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MARIUS F G RAŞ (coord.) ___________________________________________________________________________ Studii comparative privind biodiversitatea habitatelor costiere, impactul antropic şi posibilit ţile de conservare şi restaurare a habitatelor de importanţ european dintre Capul Midia şi Capul Kaliakra - Volum cu lucr rile Conferinţei de la Constanţa (Mamaia, 26-28 septembrie 2008) 2 MARIUS F G RAŞ (coord.) Studii comparative privind biodiversitatea habitatelor costiere, impactul antropic şi posibilit ţile de conservare şi restaurare a habitatelor de importanţ european dintre Capul Midia şi Capul Kaliakra Volum cu lucr rile Conferinţei de la Constanţa (Mamaia, 26-28 septembrie 2008) Editura EX PONTO Constanţa, 2008 3 Acest volum a fost realizat în cadrul proiectului RO 2005/017-535.01.02.02 prin Programul Transfrontalier Phare CBC 2005 România-Bulgaria, cu sprijinul financiar al Uniunii Europene Editor: Universitatea Ovidius Constan a B-dul Mamaia, Nr. 124, 900527, Constan a, Tel./fax. +40 241 619040, www.univ-ovidius.ro e-mail: fagarasm@univ-ovidius.ro Data public rii: noiembrie 2008 Coordonator volum: Marius F g raş Tehnoredactare şi fotografii coperţi: Marius F g raş Referenţi ştiinţifici: Prof. univ. dr. Marian Traian Gomoiu – m.c. al Academiei Române, Universitatea “Ovidius” Constan a Cp. I dr. Dumitru Murariu – m.c. al Academiei Române, Muzeul de Istorie Natural “Grigore Antipa” Prof. univ. dr. Ioan Cristurean – Universitatea Bucureşti Prof. univ. dr. Adrian Bavaru - Universitatea “Ovidius” Constan a Prof. univ. dr. Dan Cog lniceanu - Universitatea “Ovidius” Constan a Descrierea CIP a Bibliotecii Na ionale a României F G RAŞ MARIUS (coordonator) Volum cu lucr rile Conferin ei de la Constan a (Mamaia, 26-28 septembrie 2008)/ F g raş Marius (coord.) Constan a, 2008 ISBN 978-973-644-840-9 © Drepturile de autor asupra acestei publica ii sunt rezervate Universit ii Ovidius Constan a. Volumul sau p r i ale acestuia pot fi reproduse numai cu acordul autorilor. Con inutul acestui material nu reprezint în mod necesar pozi ia oficial a Uniunii Europene http://consilium.europa.eu, http://ec.europa.eu/comm/world, http://www.roinfocentre.be, http://www.infoeuropa.ro ISBN 978-973-644-840-9 4 CUPRINS Prefaţ ................................................................................................................................................. 7 Preface................................................................................................................................................. 8 Marius F g raş – General presentation of the Phare CBC project Ro 2005 – 017535.01.02.02......................................................................................................................................... 9 Marius F g raş, Paulina Anastasiu, Gavril Negrean, Zheni Nanova – Types of habitats of conservative interest and important plant associations on the sandy beaches between Cape Midia and Cape Kaliakra................................................................................................................................ 16 Paulina Anastasiu, Marius F g raş, Gavril Negrean, Zheni Nanova – Studies concerning flora of limestone plateau and cliff from Kamen Bryag-Yailata (Bulgaria)................................................ 25 Zheni NANOVA, Marius F g raş, Paulina Anastasiu, Gavril Negrean – Study of the higher flora on the territory of Kaliakra Reserve............................................................................................ 32 Gavril Negrean – Romanian botanical contributions to the studies of flora in Bulgarian Dobrogea.............................................................................................................................................. 49 Daciana Sava, Alexandru Bologa – Macrophytobenthos evolution under present environmental quality of Romanian Black Sea coastal waters as to earlier decades................................................... Dan 61 Cog lniceanu, Ciprian Samoil , Marian Tudor, Marius Skolka – Amphibians and reptiles from the Black Sea coast area between Cape Midia and Cape Kaliakra................................. 71 Marius Skolka - Invertebrate diversity in the western part of Black Sea coast: Cape Midia-Cape Kaliakra................................................................................................................................................ 90 Gabriel B nic – Study on the avifaunistical diversity in the coastal area between Cape Midia (Romania) and Cape Kaliakra (Bulgaria)............................................................................................. 111 Stoyan Nonev – The ornithofauna of seaside Bulgarian Dobroudja................................................... 123 Gabriela-Mihaela Paraschiv - Study of the Polychaeta fauna (Annelida) from the mediolittoral and infralittoral of the Black Sea: littoral segment Cape Midia-Cape Kaliakra ................................. 130 Loreley Dana Jianu, Silvia Raluca Turcu - NATURA 2000 European ecological network in Romania............................................................................................................................................... 5 140 Lucica Tofan, Timothy J. Ehlinger, Megan Helt-Baldwin, Diana Cerjak, Daniela Vasile, Richard Shaker, Mirela Bucur, Ana Maria Buiculescu - Formulation of a shoreline development index to examine the relationship between development and ecological integrity......... 144 Monica Axini, Rodica Bercu, Ligia D. Dima – Five years of activity concerning the education of the coastal lands protection.................................................................................................................. 153 Stefka Georgieva Gabrovska – Forms and methods of ecological education and upbringing .......... 158 6 Prefaţ Acest volum reuneşte o bun parte a lucr rilor ştiin ifice prezentate şi discutate în cadrul Conferin ei interna ionale organizat la Constan a (Mamaia, 26-28 septembrie 2008) în cadrul proiectului transfrontalier Phare CBC Ro 2005/ 017-535.01.02.02, proiect implementat de Universitatea “Ovidius” Constan a, în parteneriat cu Agen ia de Protec ie a Mediului Constan a şi Getia Pontica Association, ONG din oraşul Kavarna, Bulgaria. Scopul principal al Conferin ei a fost popularizarea activit ilor de cercetare desf şurate pe teren de c tre membrii echipei de proiect în zona costier transfrontalier dintre Capul Midia (România) şi Capul Kaliakra (Bulgaria), cercet ri care au vizat studiul habitatelor naturale şi al biodiversit ii costiere în complexitatea sa (flor , asocia ii vegetale, fauna de nevertebrate, herpetofauna şi avifauna). Au fost vizate de asemenea, aspecte legate de impactul antropic în zona costier , urm rindu-se g sirea unor solu ii viabile pentru diminuarea efectelor negative ale activit ilor umane în regiunea litoralului vestic al M rii Negre, concomitent cu protec ia şi conservarea habitatelor naturale, a florei şi faunei tipice acestor habitate. Studiul comparativ al biodiversit ii din zona sudic a litoralului românesc, intens antropizat şi zona nordic a litoralului bulg resc, relativ bine conservat , au confirmat faptul c o mare parte a pierderilor de biodiversitate de la litoralul românesc al M rii Negre, semnalate în literatura de specialitate şi constatate pe teren, sunt consecin a activit ilor antropice, mai ales a dezvolt rii turistice explozive din cea de-a doua jum tate a secolului XX. Situa ia actual a biodiversit ii din zona costier a Dobrogei sudice este bine reflectat în lucr rile din acest volum, lucr ri care aduc date ştiin ifice noi, dar şi confirm ri sau infirm ri ale cunoştin elor din literatura de specialitate. Principalul merit al acestui volum este faptul c reuneşte informa ie ştiin ific complex cu privire la tipurile de habitate şi biodiversitatea costier a Dobrogei româneşti şi bulg reşti, începând cu zona infralitoral , continuând cu cea mediolitoral şi supralitoral şi terminând cu zonele umede din dreptul lacurilor paramarine, cu fâşiile de step din apropierea falezei sau cu p durile şi tuf rişurile submediteraneene ale falezelor terasate din zona bulg reasc a Dobrogei. Sunt prezentate de asemenea în acest volum aspecte ale educa iei ecologice desf şurate de c tre ecologişti inimoşi, membrii ai unor ONG-uri din România şi Bulgaria, care au participat la Conferin a noastr în calitate de invita i. Sper m ca acest volum s fie bine primit în lumea ştiin ific din România şi Bulgaria, cu atât mai mult cu cât realizarea lui este rezultatul colabor rii strânse dintre specialişti români şi bulgari din diferite domenii ale Biologiei şi Ecologiei. Doresc s mul umesc pe aceast cale atât membrilor echipei de proiect şi invita ilor noştrii care au preg tit lucr ri ştiin ifice, cât şi distinşilor referen i ai volumului. coordonatorul volumului Dr. Marius Fagaras 7 Preface This volume brings together most of the scientific papers presented and discussed during the International Conference organized in Constanta (Mamaia, September 26-28, 2008), within the transborder project PHARE CBC Ro 2005/ 017-535.01.02.02, which was implemented by “Ovidius” University Constanta in partnership with the Environmental Protection Agency Constanta and Getia Pontica Association, NGO from Kavarna, Bulgaria. The main purpose of the Conference was the popularization of the field research activities the project team members accomplished in the cross-border coastal area between Cape Midia (Romania) and Cape Kaliakra (Bulgaria). These researches targeted the study of the natural habitats and coastal biodiversity in its complexity (flora, plant associations, invertebrate fauna, herpetofauna and avifauna). The field studies also targeted aspects related to the anthropogenic impact on the littoral habitats, on their specific flora and fauna, looking for viable solution and the reduction of the negative effects caused by the human activities in the western part of the Black Sea littoral, together with the protection and preservation of the natural habitats, of the wild flora and fauna. The comparative study of the biodiversity in the southern part of the Romanian littoral, intensely anthropic, and the northern part of the Bulgarian littoral, relatively well preserved, have confirmed that much of the biodiversity losses signaled in the specialized literature and noted on the field are the consequence of the anthropic activities, especially of the explosive touristic developments in the second part of the 20th century. The current situation of the coastal biodiversity of southern Dobrogea is well reflected in the papers in this volume, as they offer many new scientific data, but they also bring confirmations or contradictions of the specialty literature. The main merit of this volume is that is brings together complex scientific information regarding the coastal biodiversity of Romanian and Bulgarian Dobrogea, starting with the infra-littoral area and continuing with the mid-littoral and supra-littoral, and ending with the wetlands around the paramarine lakes, the steppe strips on and behind the seawall or the sub-Mediterranean forests and bushes of the terraced seawalls in the Bulgarian area of Dobrogea. The volume also includes aspects of ecological education accomplished by devoted ecologists, members of NGOs in Romania and Bulgaria, which participated in our Conference as guests. We hope that this volume will be well received in the scientific community in Romania and Bulgaria, as its existence is the result of the strong collaboration between Romanian and Bulgarian specialists in different fields of biology and ecology. I wish to thank the project members and the guests that prepared scientific papers for this volume, as well as the distinguished scientific reviewers of the volume. volume coordinator Marius F g raş, Ph.D. 8 GENERAL PRESENTATION OF THE PHARE CBC PROJECT RO 2005/017 – 535.01.02.02 Marius F G RAŞ, Ph.D. * Ovidius University Constanţa, the Faculty of Natural and Agricultural Sciences, Department of Biology - Ecology 124 Mamaia Blvd , Constanţa, 900527, Romania, fagarasm@yahoo.com __________________________________________________________________________________ Abstract: This cross-border project took place over a period of 14 months through the program PHARE CBC, financed by the European Union and the Romanian Government. The project was based on the partnership between “Ovidius” University Constanta, The Environmental Protection Agency (EPA) and Getia Pontica Association of Kavarna. The aim of the project was to develop a durable partnership, to have joint activities for research and monitoring of the biodiversity in the Romanian and Bulgarian coastal area of Dobrogea, to estimate the anthropogenic impact on the natural habitats, on the wild flora and fauna, as well as to find common solutions for the preservation of the habitats that have not yet been affected by human activities or to restore those affected. The project results were presented in two Conferences organized in Constanta and Kavarna and they were also published in scientific books and papers. Keywords: PHARE CBC project, coastal biodiversity, anthropogenic impact, conservation, habitats, Cape Midia, Cape Kaliakra. __________________________________________________________________________________________ Introduction The aim of our cross-border project was to establish a durable partnership between “Ovidius” University Constanta (the Faculty of Natural and Agricultural Sciences), the Environmental Protection Agency (EPA) from Constanta and the “Getia Pontica Association for Ecology and Sustainable Developement” NGO from Kavarna, Bulgaria, with the purpose of organizing joint field research, information exchanges and monitoring activities of the coastal habitats and biodiversity (flora, plant communities, fauna, birds) in the terrestrial coastal area between Cape Midia (Romania) and Cape Kaliakra (Bulgaria) (Fig. 1), on a shore length of approximately 130 km. Such a project is an interesting idea because the area between Cape Midia and Vama Veche is a touristic area, much affected by economical activities, while the area between Durankulak and Cape Kaliakra (Bulgarian Dobrogea) is relatively well preserved, with sand dune vegetation, steppe vegetation and wetlands. Our field research data, compared with that bibliographical information, will indicate the extent to which the biodiversity losses in the southern area of the Romanian Black Sea shore are due to anthropogenic factors. As a result of our studies we wrote a common Strategy for the conservation of the coastal biodiversity of Dobrogea between Cape Midia and Cape Kaliakra. The implementation of this strategy by the environmental Authorities will lead to the improvement of the management plans in the Romanian and Bulgarian coastal areas of Dobrogea. The increased involvement of local and central authorities, as well as the interest of the riverside residents in the problems of biodiversity preservation and of the conservation and restoration of natural habitats, was another objective of the project. Our collaboration with the Bulgarian partners in this field will continue in the future through joint monitoring actions, in order to ascertain the way in which the results of our collaborative actions will lead to the improvement of the management of the coastal terrestrial territory, the protected areas or other zones that are remarkable through their biodiversity. 9 Fig. 1 – The studied coastal area between Cape Midia and Cape Kaliakra Material and Methods The inventory of biodiversity from the terrestrial coastal area between Cape Midia and Cape Kaliakra has been accomplished through numerous field trips both in Romania and Bulgaria, between April and August 2008. For the determination of botanical and zoological material, the researchers used specific books such as: Flora Europaea [Tutin T.G. (eds.), vol. 1-5, 1964-1980], Flora of Romania, vol. 1-13 (Sãvulescu Tr., 19521976), The Illustrated Flora of Romania (Ciocarlan V., 2000), The Romanian Fauna, Red Data Book of the People’s Republic of Bulgaria, Volume 2- Animals (Botev et al., 1984), Red Data Book of the People’s Republic of Bulgaria, Volume 1- Plants [Velchev V. (ed.) et al., 1984], Flora of Dobrudja (Kitanov, Penev, 1980), etc. The botanical nomenclature is in accordance with the Romanian Flora and Flora Europaea. The identification of plant communities was made by means of the phytocenological survey method, in accordance with west-European methodology (Zurich-Montpellier). The names of plant communities are in accordance with the International Code of Phytosociological Nomenclature (Weber et al, 2000). In case of rare and endangered species, their threatening degree was established on the basis of Romanian Red Lists (Negrean G., 2001, Dihoru Gh., 1994, Oltean M. and al., 1994), the Red Data Book of the People’s Republic of Bulgaria, IUCN Red List of Threatened Species (2008), The Annexes of Bern Convention, Bird Directive 79/409/EEC, etc. 10 For the identification and characterization of natural coastal habitats with conservative interest we used some scientific materials, such as: The Habitats of Romania (Donita N. and al., 2005), CORINE biotopes manual: Habitats of the European Communities, 1991, Habitats Directive 92/43/EEC, A classification of Palearctic habitats (Devillers, 1997), Manual for the Interpretation of Natura 2000 Habitats in Romania (Gafta, Owen, 2008), Biodiversity of Dobrudja (Skolka et al., 2005), Threaten and Rare Plant Communities in Bulgaria (Velchev, Bondev, 1984), etc. The mapping of the coastal habitats with European conservative importance (according to the Habitats Directive) and also the rare and endangered plant populations was made by a cartographer. For the fauna diversity analysis, samples from specific terrestrial ecosystems were collected, both from the beaches and the cliffs. Quantitative samples were taken using specific methods – the entomological net for flying insects and Barber traps for terrestrial fauna. Birds, reptiles and mammals were observed “in situ” and identified with specific methods – direct observation, field guides etc. Results and Discussions In the context of the adhesion of Romania and Bulgaria to the European Union and of environmental legislation uniformity, it is necessary to elaborate plans of cross-border management that are applicable to the entire coastal zone of Dobrogea (both Romanian and Bulgarian). To this purpose, a general evaluation of the coastal biodiversity of Dobrogea is necessary. Without a systematic inventory of the flora and fauna in the southern part of the Romanian littoral and northern part of the Bulgarian seacoast, the biodiversity losses will be neither correctly estimated nor limited. There is an imperative need for a Red List of vascular plants in the littoral zone of the Romanian and Bulgarian Dobrogea, which should not take into account borders, but only the size of populations, of territory and also the risk factors. It is also necessary to identify and locate the habitats of European interest, in order to be able to impose adequate measures for conservation and restoration beyond the territorial limits of the two neighboring countries. The implementation of the “Natura 2000” European network of protected areas but also of other environmental programs has encountered difficulties (at least in Romania) because of the lack of updated information regarding the coastal biodiversity, the distribution of habitats of European interest in the littoral zone and also the rare flora and fauna species. A complete evaluation of the biodiversity in both zones of Dobrogea will permit the elaboration of a Strategy regarding the conservation of coastal biodiversity in the Romanian and Bulgarian coastal area of Dobrogea, valid on both sides of the common border. The management of the coastal zone, especially of the sites of European importance, could be much improved as a result of the books we realized. In this context, our project had the following objectives: a). The development of a durable partnership between the project partners with the purpose of realizing collaborative actions of research and monitoring of the coastal biodiversity between Cape Midia and Cape Kaliakra; b). A better knowledge of the Romanian and Bulgarian coastal area and of the management applied for the protection of biodiversity and habitats of conservative interest; c). The evaluation of the current biodiversity (flora, fauna) situation over the entire coastal area of Dobrogea, through cross-border research realized over the entire vegetation period; d). The identification, mapping and monitoring of the natural habitats of European interest, of the plant communities, of the rare plant and animal populations (in accordance with the UNEP-WCMC database, IUCN Romanian and Bulgarian Red Lists, Bern Convention) and of those areas with remarkable biodiversity; e). The identification of unprotected coastal areas with large plant and/or animal diversity and the mapping of those areas; f). The evaluation of the anthropogenic impact over the natural coastal habitats and of the biodiversity losses determined by the economical activities. 11 g). The identification of solutions for the conservation and restoration of important habitats (according to the Habitats Directive) in the coastal areas that have been strongly affected by human activities. h). The publishing of a Strategy regarding the conservation of coastal biodiversity in the Romanian and Bulgarian coastal zone of Dobrogea; this should help both the implementation of the European environmental programs in the western coastal area of the Black Sea and the improvement of the coastal management between Cape Midia and Cape Kaliakra. i). The publication of a scientific book with our scientific results and a Volume containing scientific papers presented by lecturers within the Conferences; j). the wide popularization of our joint activities and results both in Romania and Bulgaria within Conferences (organized in Constanta and Kavarna); k). A wide dissemination of the research results, as scientific papers/reports and also materials (brochure, folders) that should be easily accessible to non-specialists and common citizens. l). The Setting up of the Information Centre regarding the Dobrogea coastal biodiversity and a website (www.coastal-biodiv.ro); All these ambitious objectives could not be realized without the consistent institutional partnership and established between the Faculty of Natural and Agricultural Sciences (“Ovidius” University Constanta), the Environmental Protection Agency (EPA) and “The Association for Ecology and Sustainable Development-Getia Pontica”, NGO from Kavarna (Bulgaria). Ovidius University Constanta is a public education institution, with competences in the field of scientific research. The Faculty of Natural and Agricultural Sciences has participated in numerous projects in the field of biodiversity protection and conservation, projects that materialized in the publication of scientific books and papers. Due to the experience accumulated over time, it took responsibility for the coordination of this project. The Environmental Protection Agency Constanta is the most important local authority responsible for the implementation of environmental programs (for example, Natura 2000, Habitats Directive, etc.), of biodiversity monitoring and of administration of protected areas in Constanta district. The Association for Ecology and Sustainable Developement “Getia Pontica”, member of the environmental NGOs network in Bulgaria, is an NGO with experience in developing projects connected to sustainable development and biodiversity protection in Dobrich district. Through this NGO, the project activities included the participation of specialists from Shumen University, the Faculty of Natural Sciences. The results of our research addressed certain target groups and final beneficiaries, with competences in implementing environment programs: The Local Environmental Authority, The National Environmental Agency, The Natural Monuments Commission within the Romanian Academy, the Regional legislative authorities (District Councils), the Dobrogea-Littoral Water Department Constanta, the Environmental Guard, environmental NGOs, the riverside residents. • • • • The main activities of the project were: Meeting with all the partners in order to establish work groups, methodology and details of the activities according to the grant scheme (April 2008). Work visit to different points of the Romanian coastal area where research activities took place; Field research in the coastal zone between Cape Midia and Cape Kaliakra, between April and August 2008. Five field trips were organized in key points of the Romanian coastal zone between Cape Midia and Vama Veche and other five in the northern coastal area of Bulgaria between Durankulak and Cape Kaliakra (Fig. 1); The organization of a Conference and a round table in Constanta (September 2008), with three main objectives: the presentation of our field research results, discussions with institution participation about the draft of the Strategy for the conservation of coastal biodiversity of Dobrogea; the wide popularization and dissemination of our collaborative activities; The organization of a Conference and a round table in Kavarna (October 2008), together with our Bulgarian partners, with the purpose of popularizing and disseminating project activities and results in Bulgaria. 12 The project activities could be accomplished due to a large team of specialists from Romania and Bulgaria. • • • • • • • • • • • • • • • • • The Romanian project team Marius F G RAŞ, Ph.D. - Ovidius University of Constanta – project Manager and expert in botany, plant ecology, plant conservation; Marian-Traian GOMOIU, Ph.D. - Ovidius University of Constanta, member of the Romanian Academy, former Governor of the Danube Delta; expert in marine zoology, ecology, biodiversity conservation; Marius SKOLKA, Ph.D. - Ovidius University of Constanta; expert in zoology, marine invasive species, biodiversity conservation; Loreley Dana JIANU – Environmental Protection Agency Constanta, Biodiversity Conservation Department; expert in protected areas and environmental legislation; Dan COG LNICEANU, Ph.D. - Ovidius University of Constanta; expert in zoology, ecology, biodiversity; Paulina ANASTASIU, Ph.D. – University of Bucharest, Faculty of Natural Sciences; expert in botany, plant conservation, invasive plants; Lenuta BOBE - Ovidius University of Constanta; economist and expert in financial aspects; Olivia CHIROBOCEA - Ovidius University of Constanta; English-Romanian and Romanian-English translator/interpreter; Gavril NEGREAN - University of Bucharest, expert in botany (volunteer); Ciprian SAMOIL – Ph.D. student at Ovidius University of Constanta; IT specialist; Gabriel B NIC – Ph.D. student at Ovidius University of Constanta; ornithologist (volunteer); Marian TUDOR – Ph.D. student at Ovidius University of Constanta; zoologist (volunteer); The Bulgarian project team Georgi Yordanov GEORGIEV – Getia Pontica Association – Bulgarian team coordinator; biologist; Galin GEORGIEV – manager of Getia Pontica Association; field guide; Zheni NANOVA – “Konstantin Preslavsky” University from Shumen (Bulgaria), Faculty of Natural Sciences; expert in botany; Alexander DOYCHINOV – “Konstantin Preslavsky” University from Shumen (Bulgaria), Faculty of Natural Sciences; expert in zoology, ecology; Lenutsa MARCEA – Getia Pontica Association; Bulgarian-Romanian and Romanian-Bulgarian translator/interpreter; Conclusions Through our inventories and monitoring of the coastal biodiversity between Cape Midia and Cape Kaliakra, our project has brought numerous new data presented in the scientific books and papers published by our team members; Through its inter-human relations component, the project facilitated the cooperation between different institutions (Ovidius University of Constanta, the University of Bucharest, the University of Shumen, the Environmental Agency Constanta, etc.) and people with various specializations from Romania and Bulgaria, to the benefit of a better protected and managed environment in the cross-border area between Cape Midia and Cape Kaliakra. Through the component of dissemination and popularization of information, the project permitted the exchange of information and experience with the Bulgarian partners but also with other organizations involved in the environmental protection problem in Bulgarian and Romania. Through its strategy component, the project permitted the elaboration of a Strategy of conservation of the coastal biodiversity, as a first step towards the improvement of management plans for the western Black Sea coastal area; 13 The establishment of a website (www.coastal-biodiv.ro) and of an Information Center regarding the coastal biodiversity of Dobrogea, will facilitate the further dissemination of the environmental information through printed and ‘on line’ materials. Since our initial objectives have been reached, we consider that our cross-border project has been a success, to which every team member has brought their contribution. References 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. BOTEV B. & TZOLO PESHEV (EDS.), BOEV N., SIMEONOV S., BESHKOV V., KARAPETKOVA M., POMAKOV V., MICHEV T., 1984 - Red Data Book of the People’s Republic of Bulgaria, Volume 2. Animals, Publishing House of the Bulgarian Academy of Sciences, Sofia. CIOCÂRLAN V., 2000 – The ilustrated Flora of Romania. Pteridophyta et Spermatophyta (in Romanian), Edit. Ceres, Bucharest. DEVILLERS P., DEVILLERS-TERSCHUREN J., 1997 – A classification of Palearctic habitats. Nature and Environment, no. 78, Strasbourg, Council of Europe. DIHORU GH., DIHORU ALEXANDRINA, 1994. Plante rare, periclitate şi endemice în flora României – lista roşie, Bucureşti, Acta Botanica Horti Bucurestiensis, Lucr. Gr d. Bot., Bucureşti: 173-197. N., POPESCU A., PAUC -COM NESCU M., MIH ILESCU S., BIRIŞ A.I., 2005 – Habitats of DONI Romania (in Romanian), Edit. Tehnic Silvic , Bucharest, 496 pp. N., POPESCU A., PAUC -COM NESCU M., MIH ILESCU S., BIRIŞ A.I., 2005 – Habitats of DONI Romania (Amendaments of Habitats Directive proposed by Romania and Bulgaria) 2006, Edit. Tehnic Silvic , Bucharest, 496 pp. GAFTA D., J.O. MOUNTFORD (eds.) & (Alexiu V., Anastasiu P., B rbos M., Burescu P., Coldea Gh., Dr gulescu C., F g raş M., Gafta D., Goia I., Groza Gh., Micu D., Mih ilescu S., Moldovan O., Nicolin L.A., Niculescu M., Oprea A., Oroian S., Pauc Com nescu M., Sârbu I., Şuteu Al.), 2008 – Handbook for interpretation of Natura 2000 habitats from Romania (in Romanian), Achieved and published in the frame of the project PHARE EuropeAid/121260/D/SV/RO “Implementation of Natura 2000 network in Romania”, Edit. “Risoprint”, Cluj-Napoca, 102 pp., ISBN 978-973-751-697-8. KITANOV B., PENEV I., 1980 – Flora of Dobrudja, Publ. House “Nauka i izkustvo”, Sofia, 630 pp. (in Bulgarian). NEGREAN G., 2001 – Lista roşie a plantelor din România existente în pajişti, inclusiv endemite şi subendemite (Tracheophyta) (pg. 30-57), în Ghid pentru identificarea şi inventarierea pajiştilor seminaturale din România, Sârbu Anca (ed.) & Coldea Gh., Sârbu I., Negrean G., 2001, Ed. “alo Bucureşti!, Bucharest, 58 pp. OLTEAN M., NEGREAN G., POPESCU A., ROMAN N., DIHORU G., SANDA V., MIH ILESCU S., 1994. Lista roşie a plantelor superioare din România, Bucureşti, Studii, Sinteze, Documente de Ecologie, 1: 1-52. S VULESCU T. (ed.), 1952-1976 – Flora of Romania (in Romanian), vol. I-XIII, Edit. Academiei Române, Bucureşti. SKOLKA M., F G RAŞ M., PARASCHIV GABRIELA, 2005 – Biodiversity of Dobrudja (in Romanian), Ovidius University Press, Constan a, 396 pp., ISBN 973-614-232-9. TUTIN T.G. (eds) & colab., 1964-1980 - Flora Europaea, Vols. 1-5, Cambridge, Cambridge University Press. TUTIN T.G. (eds) & colab. - Flora Europaea, 2nd ed., Vol. 1, Cambridge, Cambridge University Press. VELCHEV V, BONDEV I., 1984 - Threaten and Rare Plant Communities in Bulgaria (in Bulgarian; abstract in English). Savremenni Teoret. i Prilojni Aspecti na Rast. Ecologija (Modern Theoretical and Applied Aspects of the Plant Ecology). Sofia. 1:94-105. VELCHEV V. (ED.) & KOZUHAROV, BONDEV I., KUZMANOV B., MARKOVA M., VELEV V., 1984 – Red Data Book of the People’s Republic of Bulgaria, Volume 1. Plants, Publishing House of the Bulgarian Academy of Sciences, Sofia. 14 17. WEBER H.E., MORAVEC J., THEURILLAT J.P., 2000 – International Code of Phytosociological Nomenclature, 3 Ed. –J. Veg. Sci., 11 (5) :739-768. 18. *** OUG 57/2007 (OUG regarding protected areas, conservation of natural habitats and of wild flora and fauna). 19. *** Habitats Directive 92/43/EEC – Council Directive 92/43/EEC on the conservation of natural habitats and of wild Fauna and flora. 20. *** IUCN Red List of Threatened Species 2008 - http://www.iucnredlist.org 21. *** Habitats Directive 92/43/EEC – Council Directive 92/43/EEC on the conservation of natural habitats and of wild Fauna and flora. 22. *** Birds Directive 79/409/EEC – Council Directive 92/43/EEC on the conservation of wild birds. 23. *** 1991, CORINE Biotopes Manual – Habitats of the European Community. 24. *** The Bern Convention on the Conservation of the European Wildlife and Natural Habitats, 1979. 15 TYPES OF HABITATS OF CONSERVATIVE INTEREST AND IMPORTANT PLANT ASSOCIATIONS ON THE SANDY BEACHES BETWEEN CAPE MIDIA AND CAPE KALIAKRA Marius F G RAŞ*, Paulina ANASTASIU**, Gavril NEGREAN**, Zheni NANOVA*** * Ovidius University Constanţa, Faculty of Natural and Agricultural Sciences, Dept. of Biology - Ecology 124 Mamaia Blvd, Constanţa, 900527, Romania, fagarasm@yahoo.com ** University of Bucharest, Faculty of Biology, Dept. of Botany & Microbiology, 1-3 Aleea Portocalelor , Bucharest, 060101, Romania, anastasiup@yahoo.com *** University of Shoumen, Faculty of Natural Sciences, 115 "Universitetska" Street, Shoumen 9712, Bulgaria, jenidim@gmail.com __________________________________________________________________________________________ Abstract: This paper includes a characterization of all the main types of habitats of European interest, including the priority natural habitats referred to in Annex I of the Habitats Directive and identified in the area of sandy beaches between Cape Midia and Cape Kaliakra. Six types of habitats of conservative interest are characterized, as they are distributed especially in the broad sandy beaches in the proximity of the littoral lakes (Lake Corbu, Lake Siutghiol, Lake Techirghiol, Herghelie Marsh Mangalia, Lake Durankulaka and Lake Shabla). For each type of habitat, the following are specified: the characteristic plant associations, the distribution, the conservation state, the tendency in the conservation state and the main risk factors. The data in this paper are the result of field observations accomplished between April-August 2008, within the transborder project Phare CBC RO 2005/017-535.01.02.02. Keywords: habitats, plantassociations, conservation, Black Sea shore, sandy beaches, Cape Midia (Romania), Cape Kaliakra (Bulgaria). __________________________________________________________________________________________ Introduction The coastal area between Cape Midia and Cape Kaliakra, with a length of approximately 130 km, is heterogenous from the point of view of the physico-geographical conditions, with sandy beaches, wetlands, loess seawalls, limestone seawalls and limestone plateaus with steppe vegetation. The variety of the substrate and of the soil is reflected in the diversity of the natural habitats and in the large number of plant communities that populate them, many of them of European importance from the conservation point of view, according to the Directive 92/43/CEE (the Habitats Directive). Due to the expansion of the touristic resorts, of the abusive construction in the beach area, but also to the lack of a coherent strategy for preservation and sustainable management, the coastal phytodiversity in the Romanian littoral area south of Cape Midia has known a strong decline over the past 15 years. The destruction or serious damage of the natural habitats has led to the disappearance of communities of typically littoral plants and of species of rare psamophile plants at national or European level (that were indicated in this area in bibliographical papers). In the northern coastal part of Bulgaria, the anthropogenic influences are relatively reduced due to the large surfaces occupied by protected areas: the Lake Dunakulak Natural Complex, the Shabla Complex, the Yailata Natural Reserve and the Kaliakra Reserve. Consequently, the natural habitats are well preserved and they shelter a large diversity of plants, some of them floral rarities already extinct or critically endangered in the southern part of the Romanian littoral. We will mention among these species: Silene thymifolia, Stachys maritima, Euphorbia paralias, Hypecoum procumbens, Ammophila arenaria ssp. arundinacea, Corispermum 16 nitidum, Chamaesycae peplis, Cakile maritima ssp. euxina, etc. The important local populations of these species in the Durankulak Reservation (only 6-8 km south of Vama Veche) demonstrate that their decline in the Romanian littoral is mainly a consequence of the human activities that led to the degradation of the natural habitats. In this paper, we wish to describe the main habitats of conservative interest in the sandy beaches between Cape Midia (Romania) and Cape Kaliakra (Bulgaria) (Fig. 1), to present their specific plant associations and the risk or potential factors that may determine a rapid degradation of the vegetal blanket in the studied coastal area. We also wish to draw the attention to some areas with high concentration of habitats of conservative interest at EU level (Corbu-Cape Midia, Durankulak, Shabla), where touristic resorts are being built, infringing thus upon their status of protected areas. Fig. 1 – Sandy beaches with habitats of conservative interest between Cape Midia and Cape Kaliakra (the white points) Material and Methods Among the natural habitats inventoried in the coastal area between Cape Midia and Cape Kaliakra, those of conservative interest at EU level were selected. They require a designation as special conservation areas (ASC), according to Annex I of the Habitats Directive and to Annex II of OUG no. 57/2007. For all the described types of habitats, the Natura 2000 codes were specified (from the Habitats Directive) and the codes in the Palearctic Habitats classification system (Pal.Hab.) (Devillers et al., 1996). The conservation status of the habitat described was appreciated with one of the following qualifiers: very good, good, satisfactory and 17 unsatisfactory. The tendencies in the preservation state of the habitat were appreciated thus: strong decline, small decline, stable, small improvement, improvement. The specification of the plant associations characteristic to each type of habitat, to the chorological data and to the conservation state were based on the specialized bibliography (Doni et al., 2005, 2006; Gafta, Mountford et al., 2008; Tzonev et al, 2005, Velchev, Bondev, 1984; Tutin (ed.) et al., 1964-1980; S vulescu (ed.) et al., 1952-1976; Ciocârlan, 2000; Kitanov, Penev, 1980; Meshinev et al., 1991; Sanda et al., 2001; Georgiev et al., 1998; F g raş, 2002, 2003; Skolka et al., 2005) but also on the personal observations and field experience of the paper authors. The names of the plant associations are in accordance with the International Code of Phytosociological Nomenclature (Weber et al., 2000). Results and Discussions The following types of ecosystems are found in the cross-border coastal area between Cape Midia and Cape Kaliakra: • • • • • Wide sandy beaches with psammophile vegetation in the place of former sea bays (Corbu beach) or in the area of the paramarine lakes (Tasaul, Siutghiol, Techirghiol, Belona, Herghelie Marsh Mangalia, Durankulak, Shabla, etc.); Large wetlands with mesophile and higrophile vegetation behind the dune strips or in the vicinity of the paramarine lakes (Hergheliei Marsh, Lake Techirghiol, Lake Durankulak, Lake Shabla); Narrow beaches with psammophile vegetation at the base of the high seawalls (Constanta, TuzlaCostinesti, Vama Veche, Durankulak, Krapets); Low-height loess seawalls (maximum 30 m) with steppe vegetation between Cape Midia and Krapets; Steep or terraced limestone seawalls (heights of 70-80 m) with steppe vegetation and vest-pontic shrubs between Kamen Bryag and Cape Kaliakra; Among the coastal ecosystems, we will refer only to the area of sandy beaches (supralittoral) covered by psamophile vegetation, where there are several types of natural habitats of conservative interest. The largest part of the sandy beaches is covered by sand dunes and sandy belts, mobile, semifixed or stabilized by psamophile vegetation. Among the dunes and behind the dune strips, there are low areas, with stronger humitity and salinity, swampy in the heavy rain periods (especially in spring); the substrate turns into a swamp also because of the phreatic waters. Large wetlands with sandy substrate are also located in the vicinity of the littoral lakes, former river-marine lagoons (Lake Corbu, Lake Siutghiol, Lake Techirghiol, Herghelie Marsh, Lake Durankulak and Lake Shabla). The marine shore area, populated by specific vegetation, is located between the sand dunes and the sea. In the southern Romanian coastal area (Cape Midia-Vama Veche), the dune habitats were mostly destroyed during the 1960s-1970s through the extension of the touristic resorts. This kind of habitats has remained in scattered fragments in the shape of “oases” between the resorts. The situation of these “natural vegetation oases” has worsened drastically since 1995. Currently, the habitats of European interest, some even priority, are endangered because of the building of residential complexes or touristinc points of interest exactly in the area of dune habitats, as it happens between Mamaia and Navodari, North Eforie and South Eforie, 2 Mai and Vama Veche. This is why the situation of beach biodiversity in the southern area of the Romanian littoral is currently disastrous, even after the implementation of the Natura 2000 program in Romania. The dune habitats are well preserved only in the Agigea Marine Dunes Reservation, natural reserve with a surface of 8 ha. In the northern Bulgarian coastal area, the dune habitats are well represented on the large sandy beaches in front of the littoral Lakes Durankulak and Shabla. In the seawall areas, where the beaches narrow considerably, the presence of this kind of habitats is reduced. In accordance with Directive 92/43 CEE and OUG 57/2007, the natural habitats of conservative interest are classified as follows: 18 1). Natural habitats of European interest – those types of habitats that: • are endangered in their natural distribution area; • have a reduced distribution surface; • are representative samples for one or more of the five biogeographical regions specific to Romania: alpine, continental, Pannonial, steppe and Pontic (the Black Sea region). 2). Priority natural habitats – types of endangered natural habitats, for whose conservation, the European Community has a particular responsibility, due to the reduced proportion of their area on the European Union territory. • these types of habitats are indicated by an asterisk (*) in Annex I of the Habitats Directive and in Annex II of OUG 57/2007 (OUG regarding the regime of the protected natural areas, the conservation of the natural habitats and of the wild flora and fauna). In the sandy beaches (supralittoral) area between Cape Midia and Cape Kaliakra, six types of habitats of conservative interest have been identified (Tab. 1). According to the Habitats Directive (Directive 92/43 CEE), they require the designation of Special Conservation Areas (SAC) which must be include in the Natura 2000 European ecological network: • • • • • • Annual vegetation of drift lines (Code Natura 2000: 1210; code Pal. Hab: 17.2) Embryonic shifting dunes (Code Natura 2000: 2110; code Pal. Hab: 16.211) Shifting dunes along the shore line with Ammophila arenaria (white dunes) (Code Natura 2000: 2120; code Pal. Hab: 16.212); Fixed coastal dunes with herbaceous vegetation (grey dunes) (Code Natura 2000: * 2130; code Pal. Hab: 16.221-16.227, 16.22B); Humid dune slacks (Code Natura 2000: 2190; code Pal. Hab: 16.3); Mediterranean salty meadows (Juncetalia maritimi) (Code Natura 2000: 1410; code Pal. Hab: 15.5); These types of habitats characteristic to the sandy beaches between Cape Midia and Cape Kaliakra will be described in what follows. 1210. Annual vegetation of drift lines Characteristics: include plant communities which grow on coarse sand, slightly salty and rich in nitrate substances; they cover the space between the midlittoral and the first strip of dunes. Distribution: over the entire shore length between Cape Midia and Cape Shabla, including the narrow beaches at the base of seawalls. North of Cape Shabla, the presence of this habitat type can be found only occasionally, on the narrow beaches from the bay area (Russalka, Bolata, Kavarna). Conservation state: good (in Romania and Bulgaria); Tendency in the conservation state of the habitat: stable (both in Romania and Bulgaria); Risk factors: natural (big waves, strong winds) and anthropogenic; Characteristic plant associations: it includes plant communities from the class Cakiletea maritimae R.Tx. et Prsg 1952, as well as Cakilo euxinae-Salsoletum ruthenicae Vicherek 1971, Atripliceto hastataeCakiletum euxinae Sanda et Popescu 1999; Salsolo-Euphorbietum paralias Pignatti 1952 ssp. salsoletosum ruthenicae Pop 1985; Tournefortietum sibiricae Popescu et Sanda 1975; Lactuco tataricae-Glaucietum flavae Dihoru et Negrean 1976. 19 2110. Embryonic shifting dunes Characteristics: type of habitat made up of high, mobile dunes, partially or not at all fixed by vegetation; the solidification process is in its first stages. The microclimate is characterized by considerable thermal contrasts between night and day, intense solar radiation during the day and low humidity. Distribution: in several points of the marine shore between Cape Midia and Cape Kaliakra, especially in areas with wide sandy beaches, lacking seawall or with a seawall far away from the sea; type of habitat present on the beaches of Corbu-Cape Midia, N vodari, Mamaia, North Eforie, South Eforie, Durankulak, Shabla, Krapets, Bolata bay. Conservation state: unsatisfactory in the Romanian southern coastal area, good in the northern Bulgarian area; seriously affected habitat in the beach area between Mamaia-Navodari, North Eforie and South Eforie and 2 Mai-Vama Veche by the construction of residences and touristic activities. Trend in the conservation state of habitat: stable (both in Romania and Bulgaria); Risk factors: natural (strong winds) and anthropogenic (buildings, sand extraction); Characteristic plant associations: Elymetum gigantei Morariu 1957; Leymo sabulosi-Elymetum farcti Gehu et al. 1986, Artemisietum tschernievianae (arenariae) Popescu et Sanda 1977; Secali sylvestris-Alyssetum borzeani (Borza 1931) Morariu 1959; Aperetum maritimae Popescu et al. 1980; Secali sylvestris-Brometum tectorum Hargitai 1940; Crambetum maritimae (Şerb nescu 1965) Popescu et al. 1980, Convolvuletum persici (Borza 1931) Burduja 1968. 2120. Shifting dunes along the shoreline with Ammophila arenaria (white dunes) Characteristics: Habitat of high, mobile or semi-fixed dunes, generally populated by psamophile species of the alliance Ammophilion arenariae J. M. et J. Gt. 1969 and Elymion gigantei Morariu 1957; Distribution: only in the Bulgarian coastal area, between Durankulak and Shabla; they do not exist in the Romanian coastal area; the Durankulak beach (the Cosmos camp) is the northernmost point where Ammophila arenaria ssp. arundinacea was noticed; Conservation state: very good, due to the small touristic developments in the northern coastal area of Bulgaria; Trend in the conservation state of habitat: stable; Risk factors: natural (strong winds) and anthropogenic (buildings, sand extraction); Characteristic plant associations: Ammophilo arundinaceae-Elymetum gigantei Vicherek 1971, Festucetum beckeri Sanda, Popescu 1997; 2130. Fixed coastal dunes with herbaceous vegetation (grey dunes) (priority habitat) Characteristics: coastal habitat made up of low dunes, stabilized and fixed by vegetation, located behind the strips of mobile dunes; the solidification process is advanced. In this habitat type grow usually plant associations of the class Festucetea vaginatae Soó 1968. Distribution: only in the area of wide beaches in the vicinity of paramarine lakes (the beaches of CorbuCape Midia, N vodari, Mamaia, Durankulak and Shabla). This type of habitat was completely destroyed by the extension of the resorts in the Romanian coastal area north of Mamaia. Conservation state: good in the Bulgarian coastal area, unsatisfactory south of Cape Midia, except the Agigea Marine Dunes Reservation where is good. Trend in the conservation state of habitat: stable (both in Romania and Bulgaria); Risk factors: natural (strong winds) and anthropogenic (buildings, sand extraction; garbage disposal on the beach); 20 Characteristic plant associations: Scabioso argenteae-Caricetum colchicae (Simon 1960) Krausch 1965; Ephedro-Caricetum colchicae (Morariu 1959) Krausch 1965; Caricetum colchicae Simon 1960; Scabioso argenteae-Artemisietetum campestris Popescu et Sanda 1987; Plantaginetum arenariae (Buia et al. 1960) Popescu et Sanda 1987; Stachyo atherocalici-Caricetum ligericae Tzonev & al., 2005. 2190. Humid dune slacks Characteristics: type of low habitat located located between dunes, with slightly salty soils and high humidity conditions; the solidification process is advanced. Distribution: in the proximity of the wide beaches of the paramarine lakes (Corbu, Navodari, Mamaia, Herghelie Marsh, Durankulak and Schabla). This habitat does not exist in the coastal areas with seawall. Conservation state: satisfactory in the Romanian southern coastal area and very good in the Bulgaria; Trend in the conservation state of habitat: small decrease in Romania and stable in Bulgaria; Risk factors: anthropogenic (buildings, garbage disposal on the beach); Characteristic plant associations: Orchio-Schoenetum nigricantis Oberd. 1957, HoloschoenoCalamagrostietum epigeji Popescu et Sanda 1978; Lythro-Calamagrostidetum epigei I.Pop 1968, Caricetum distantis Rapaics 1927. 1410. Mediterranean salt meadows (Juncetalia maritimi) Characteristics: type of habitat populated by halophile species with sandy-clay or silty soils, low to medium salty, swamped in spring but dry during summer. Distribution: in the wet, salty, depression areas of beach, behind the dune strips. Habitat present especially in the wet and salty areas in the vicinity of the littoral lakes (Corbu, Navodari, Mamaia, Herghelie Marsh, Durankulak and Shabla). Conservation state: satisfactory in the Romanian coastal area and very good in the Bulgarian one. The habitat has been destroyed almost completely between Mamaia and N vodari. Trend in the conservation state of habitat: stable in Romania and Bulgaria; Risk factors: anthropogenic; Characteristic plant associations: Juncetum littoralis-maritimi Sanda et al. 1998; Juncetum littoralis Popescu et al. 1992; Juncetum maritimi (Rubel 1930) Pignatti 1953; Teucrio-Schoenetum nigricantis Sanda et Popescu 2002. Conclussions Six types of habitats of European conservative interest have been identified in the sandy beach area between Cape Midia and Cape Kaliakra. They could be easily identified especially by the plant communities that populate them. On the southern Romanian littoral, the habitats of European importance are fragmented among the resorts and are well represented especially in the wide beaches nearby the paramarine lakes. On the northern Bulgarian littoral, they are well represented especially in the vicinity of Lakes Durankulak and Shabla. The preservation state of the habitats nearby the sandy beaches is generally unsatisfactory in the southern Romanian coast and good and very good in the northern Bulgarian coast. In the Romanian coastal area south of Cape Midia, the conservation of the habitats of European interest is accomplished accordingly only in the Agigea Marine Dunes Reservation. The tendencies in the conservation state of the habitats in the Romanian coastal area are negative (decline of habitats), while in the Bulgarian coastal area they are generally stable. 21 The favorable conservation state of the natural habitats, but also of the flora and fauna species in the vicinity of Lakes Durankulak and Shabla, is explained by their status as protected areas and thus by the reduced human activities in these areas. References 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. CIOCÂRLAN V., 2000 – The ilustrated Flora of Romania. Pteridophyta et Spermatophyta (in Romanian), Edit. Ceres, Bucharest. DEVILLERS P., DEVILLERS-TERSCHUREN J., 1997 – A classification of Palearctic habitats. Nature and Environment, no. 78, Strasbourg, Council of Europe. N., POPESCU A., PAUC -COM NESCU M., MIH ILESCU S., BIRIŞ A.I., 2005 – Habitats of DONI Romania (in Romanian), Edit. Tehnic Silvic , Bucharest, 496 pp. N., POPESCU A., PAUC -COM NESCU M., MIH ILESCU S., BIRIŞ A.I., 2005 – Habitats of DONI Romania (Amendaments of Habitats Directive proposed by Romania and Bulgaria) 2006, Edit. Tehnic Silvic , Bucharest, 496 pp. F G RAŞ M., 2002 – Contributions regarding ecology of flora and plant communities from the Romanian Black Sea coast. Doctoral thesis (in Romanian), “Ovidius” University of Constan a, Faculty of Natural Sciences: 258 pp+25 anexe, 64 fig., 64 tab. (manuscris). F G RAŞ M., 2003 - The conspectus of plant associations from the Romanian Black Sea shore, “Ovidius” University Annals of Biology-Ecology series, Constanta, 7 (2003): 133-138. F G RAŞ M., 2002 - The main vegetation types and plant communities from the southern Romanian Black Sea shore area (in Romanian), “Ovidius” University Annals, Biology-Ecology series, Constanta, 6 (2002): 51-62. GAFTA D., J.O. MOUNTFORD (eds.) & (Alexiu V., Anastasiu P., B rbos M., Burescu P., Coldea Gh., Dr gulescu C., F g raş M., Gafta D., Goia I., Groza Gh., Micu D., Mih ilescu S., Moldovan O., Nicolin L.A., Niculescu M., Oprea A., Oroian S., Pauc Com nescu M., Sârbu I., Şuteu Al.), 2008 – Handbook for interpretation of Natura 2000 habitats from Romania (in Romanian), Achieved and published in the frame of the project PHARE EuropeAid/121260/D/SV/RO “Implementation of Natura 2000 network in Romania”, Edit. “Risoprint”, Cluj-Napoca, 102 pp., ISBN 978-973-751-697-8. GEORGIEV D. & DERELIEV S., HAYNADJIEVA V., 1998 - Durankulak Lake Natural Complex (Management plan), Bulgarian-Swiss Biodiversity Conservation Programme (Northern coastal wetlands project). GEORGIEV D. & DERELIEV S., HAYNADJIEVA V., 1998 – Shabla Lake Complex (Management plan), Bulgarian-Swiss Biodiversity Conservation Programme (Northern coastal wetlands project). GEORGIEV D. & DERELIEV S., HAYNADJIEVA V., 1998 – Kaliakra Reserve (Management plan), Bulgarian-Swiss Biodiversity Conservation Programme (Northern coastal wetlands project). KITANOV B., PENEV I., 1980 – Flora of Dobrudja, Publ. House “Nauka i izkustvo”, Sofia, 630 pp. (in Bulgarian). MESHINEV T., MILEVA M., SPIRIDONOV G., VASSILEV P., TEKKE R., 1991 - Sand Dune Inventory of Europe. Bulgaria. :71-73. (Engl.) Ed. DT. I. P. Doody. EUCC. SANDA V., POPESCU A., STANCU I., 2001 – The coenotic structure and ecological characterisation of plant communities from Romania (in Romanian), Edit. Conphis, Bucharest, 359 pp. S VULESCU T. (ed.), 1952-1976 – Flora of Romania (in Romanian), vol. I-XIII, Edit. Academiei Române, Bucureşti. SKOLKA M., F G RAŞ M., PARASCHIV GABRIELA, 2005 – Biodiversity of Dobroudja (in Romanian), Ovidius University Press, Constan a, 396 pp., ISBN 973-614-232-9. TZONEV R., DIMITROV M., Roussakova V., 2005 – Dune vegetation of the Bulgarian Black Sea coast, Hacquetia, Warsaw, 4, (1): 7-32. 22 18. TUTIN T.G. (eds) & colab., 1964-1980 - Flora Europaea, Vols. 1-5, Cambridge, Cambridge University Press. 19. TUTIN T.G. (eds) & colab. - Flora Europaea, 2nd ed., Vol. 1, Cambridge, Cambridge University Press. 20. VELCHEV V, BONDEV I., 1984 - Threaten and Rare Plant Communities in Bulgaria (in Bulgarian; abstract in English). Savremenni Teoret. i Prilojni Aspecti na Rast. Ecologija (Modern Theoretical and Applied Aspects of the Plant Ecology). Sofia. 1:94-105. 21. WEBER H.E., MORAVEC J., THEURILLAT J.P., 2000 – International Code of Phytosociological Nomenclature, 3 Ed. –J. Veg. Sci., 11 (5) :739-768. 22. *** OUG 57/2007 (OUG regarding protected areas, conservation of natural habitats and of wild flora and fauna). 23. *** Habitats Directive 92/43/EEC – Council Directive 92/43/EEC on the conservation of natural habitats and of wild Fauna and flora. 23 Tab. 1 - Coastal habitats from Cape Midia-Cape Kaliakra seashore area and their specific plant associations Code Natura 2000 1210 Annual vegetation of drift lines Code Palearctic Habitats 17.2 2110 Embryonic shifting dunes 16.211 2120 Shifting dunes along the shore line with Ammophila arenaria (white dunes) Fixed coastal dunes with herbaceous vegetation (grey dunes) 16.212 16.221,16. 227, 16.22B 2190 Humid dune slacks 16.3 1410 Mediterranean salty meadows (Juncetalia maritimi) 15.5 * 2130 Coastal habitat type 24 Typical plant associations Cakilo euxinae-Salsoletum ruthenicae Vicherek 1971, Atripliceto hastatae-Cakiletum euxinae Sanda et Popescu 1999; Salsolo-Euphorbietum paralias Pignatti 1952 ssp. salsoletosum ruthenicae Pop 1985; Tournefortietum sibiricae Popescu et Sanda 1975; Lactuco tataricae-Glaucietum flavae Dihoru et Negrean 1976. Elymetum gigantei Morariu 1957; Leymo sabulosiElymetum farcti Gehu et al. 1986, Artemisietum tschernievianae (arenariae) Popescu et Sanda 1977; Secali sylvestris-Alyssetum borzeani (Borza 1931) Morariu 1959; Aperetum maritimae Popescu et al. 1980; Secali sylvestris-Brometum tectorum Hargitai 1940; Crambetum maritimae (Şerb nescu 1965) Popescu et al. 1980, Convolvuletum persici (Borza 1931) Burduja 1968. Ammophilo arundinaceae-Elymetum gigantei Vicherek 1971, Festucetum beckeri Sanda, Popescu 1997; Scabioso argenteae-Caricetum colchicae (Simon 1960) Krausch 1965; Ephedro-Caricetum colchicae (Morariu 1959) Krausch 1965; Caricetum colchicae Simon 1960; Scabioso argenteae-Artemisietetum campestris Popescu et Sanda 1987; Plantaginetum arenariae (Buia et al. 1960) Popescu et Sanda 1987; Stachyo atherocaliciCaricetum ligericae Tzonev & al., 2005. Orchio-Schoenetum nigricantis Oberd. 1957, Holoschoeno-Calamagrostietum epigeji Popescu et Sanda 1978; Lythro-Calamagrostidetum epigei I.Pop 1968, Caricetum distantis Rapaics 1927. Juncetum littoralis-maritimi Sanda et al. 1998; Juncetum littoralis Popescu et al. 1992; Juncetum maritimi (Rubel 1930) Pignatti 1953; TeucrioSchoenetum nigricantis Sanda et Popescu 2002. STUDIES CONCERNING FLORA OF LIMESTONE PLATEAU AND CLIFF FROM KAMEN BRYAG – YAILATA (BULGARIA) Paulina ANASTASIU*, Marius F G RAŞ**, Gavril NEGREAN*, Jheni NANOVA*** *University of Bucharest, Faculty of Biology, Department of Botany & Microbiology, Aleea Portocalelor nr. 1-3, sector 6, Bucharest, Romania, anastasiup@yahoo.com **Ovidius University of Constanţa, Faculty of Natural and Agricultural Sciences, Constanţa 900552, Romania ***University of Shoumen, Faculty of Natural Sciences, str. "Universitetska" 115, Shoumen 9712, Bulgaria __________________________________________________________________________________________ Abstract: During the field research carried out on Kamen Bryag – Yailata territory (NE Bulgaria), we inventoried 338 species and subspecies of vascular plants. Most of them are therophytes and hemicryptophytes, characteristic for grasses communities in area with dry climate. An important percent of flora is represented by Steppe elements and with southern origin (Mediterranean, sub-Mediterranean, Balkan), correlated with the climate of this region. The high number of rare and protected plants (37 taxa) makes this area valuable for conservation process. Key words: vascular plants, life forms, geo-elements, protected species, Kamen Bryag – Yailata, NE Bulgaria. __________________________________________________________________________________________ Introduction Kamen Bryag – Yailata area is situated at 18 km north-eastern of Kavarna city and is included into the natural geographic subregion of the Northern Bulgarian Black Sea Coast (Fig. 1). In geological terms this territory is part of the Moesian platform (Georgieva, Vladev, 2007; Geography of Bulgaria, 1982). Here mainly chalky sandstones and marls, middle Sarmatian marly clay and sands are disclosed (Geomorphological Map of Bulgaria) and separate areas with late sarmatian shellfish limestone. East of this territory is established one of the most typical shelves slides with submeridional direction (one of the most dangerous earthquake zones in Bulgaria). Landslides and underground niches are characteristic for cliffs. The soil on the seaside ledge is humus-calcareous. The climate is temperate-continental, but with significant humidity – Black Sea climatic region. The average air temperatures in January are positive, little higher than those inside the coastal Dobrudja. The average temperature amplitude is not high (the average annual air temperature is + 11 °C). The amount of the annual rainfall rarely exceeds 500 mm (rainfall maximum in February). The snow cover is not retained. Surface fluent waters missing due to the karstic terrain (Georgieva, Vladev, 2007; Geography of Bulgaria, 1982). According to decree 822/2002, Yailata is a protected area. It covers 45.3 ha offering historical and natural attractions. Species of animal and plants, as well as their habitats are protected here. The habitats include communities of grasses with steppic character (Bondev, 1991), forests and shrub formations, coastal limestone cliffs and caves. On the territory of this protected area, according with the information from the reserve entrance, there are 19 rare and threatened plant species, including Alyssum borzaeanum, Goniolimon besserianum, Goniolimon tataricum, Limonium latifolium, Limonium meyeri, Opopanax chironium subsp. bulgaricum and also endemic plants Silene caliacrae and Centaurea caliacrae. To Yailata the biggest subpopulation of Paeonia peregrina in Bulgaria is also protected. For Northern Bulgarian Black Sea Coast there are many botanical studies or information (Pan u, 1925; Prodan, 1935; Prodan, 1936; Prodan, 1939; Paşcovschi, 1938; Kitanov, Penev, 1980; Assyov, Petrova, 2006), but for Kamen Bryag – Yailata territory only few special references exist (Kozhuharov et al., 1997; Kozhuharov et al., 2001). 25 Fig. 1 – The geographic position of Kamen Bryag – Yailata region Material and Methods This study was carried out in the April – October 2008 period, using transects method. Transects were outlined so as to cover the maximum area. The length of researched seashore is about 5 km, between 43°27'59"N, 28°33'58"E and 43°25'35"N, 28°31'53"E. Various biotopes were studied: stony grassland from the plateau, vegetal formations of the rocky cliffs, forest and ruderal places too. For rare plants we registered the coordinates in WGS 84 system, using a GPS Garmin eTrex Legend C. The nomenclature of taxa is according to Flora Europaea (Tutin et al., 1993 ; Tutin et al., 1964-1980). The floristic elements are according to Assyov & Petrova (2006) and Ciocârlan (2000). The life form for each taxon is given after Ciocârlan (2000). Rare and threatened species are according to Red Data Book of Bulgaria [Velchev (ed.), 1984], Biodiversity law and European legislation (The Bern Convention; Council Directive 92/43/EEC; IUCN Red List of Threatened Species, 2008) Results and Discussions On the research territory we recorded the next 327 taxa: Acer campestre, Achillea clypeolata, Achillea setacea, Acinos arvensis, Adonis flammea, Aegilops cylindrica, Aegilops geniculata [syn. Aegilops ovata], Agrimonia eupatoria, Agropyron cristatum subsp. pectinatum, Ailanthus altissima, Ajuga chamaepytis, Ajuga laxmannii, Alliaria petiolata, Allium flavum subsp. flavum, Allium moschatum, Allium saxatile, Althaea cannabina, Alyssum desertorum, Alyssum hirsutum, Amaranthus crispus, Amaranthus retroflexus, Anthemis austriaca, Anthemis cotula, Anthemis tinctoria, Arabis hirsuta, Arctium lappa, Arenaria serpyllifolia, Artemisia absinthium, Artemisia austriaca, Artemisia pedemontana, Artemisia santonicum, Artemisia vulgaris, Arum orientale, Asparagus verticillatus, Asperugo procumbens, Asperula tenella, Asphodeline lutea, Asplenium rutamuraria, Aster oleifolius, Astragalus hamosus, Atriplex oblongifolia, Atriplex tatarica, Ballota nigra subsp. nigra, Bassia prostrata [syn. Kochia prostrata], Beta trigyna, Bombycilaena erecta, Brassica juncea s.l., Bromus japonicus, Bromus squarrosus, Bromus sterilis, Bromus tectorum, Buglossoides arvensis subsp. sibthorpiana [syn. Lithospermum arvense subsp. sibthorpianum], Buglossoides purpurocaerulea [syn. 26 Lithospermum purpurocaeruleum], Camelina rumelica, Campanula rapunculus, Campanula sibirica, Cardaria draba subsp. draba, Carduus pycnocephalus, Carduus thoermeri, Carpinus orientalis, Carthamus lanatus, Celtis australis, Centaurea alba subsp. caliacrae, Centaurea diffusa, Centaurea napulifera subsp. thirkei, Centaurea salonitana, Centaurea solstitialis, Cephalaria transylvanica, Cephalaria uralensis, Cerastium glomeratum, Cerastium pumilum, Chamaecytisus jankae, Chenopodium album, Cichorium intybus, Clematis vitalba, Clypeola jonthlaspi, Conium maculatum, Consolida orientalis [syn. Delphinium orientale], Consolida regalis s.l., Convolvulus arvensis, Convolvulus cantabrica, Convolvulus lineatus, Conyza canadensis, Cornus mas, Corydalis solida, Crataegus monogyna, Crepis foetida subsp. rhoeadifolia, Crepis sancta, Crithmum maritimum, Crocus pallasii, Cruciata laevipes, Crupina vulgaris, Cynanchum acutum, Cynodon dactylon, Cynoglossum creticum, Cynoglossum officinale, Dactylis glomerata s.l., Datura stramonium, Descurainia sophia, Desmazeria rigida [syn. Scleropoa rigida], Dianthus giganteus, Dianthus leptopetalus, Dianthus pseudarmeria, Dichanthium ischaemum, Digitalis lanata, Echinochloa crus-galli, Echinops ritro subsp. ruthenicus, Echinops sphaerocephalus, Echium italicum, Echium vulgare, Elymus elongatus [syn. Agropyron elongatum], Elymus hispidus, Elymus repens [syn. Agropyron repens], Ephedra distachya subsp. monostachya, Erodium ciconium, Erodium cicutarium, Erophila verna s.l., Eryngium campestre, Erysimum cuspidatum, Erysimum diffusum, Eupatorium cannabinum, Euphorbia agraria, Euphorbia helioscopia, Euphorbia myrsinites, Euphorbia nicaeensis s.l., Euphorbia seguieriana, Falcaria vulgaris, Festuca arundinacea subsp. orientalis, Festuca valesiaca, Ficus carica, Filipendula vulgaris, Fragaria viridis, Fraxinus ornus, Fumaria kralikii, Fumaria rostellata, Galanthus elwesii, Galium album subsp. pycnotrichum, Galium aparine, Galium flavescens, Galium glaucum, Galium verticillatum, Geranium molle, Geranium pyrenaicum, Geranium robertianum, Geranium rotundifolium, Geum urbanum, Gleditsia triacanthos, Goniolimon besserianum, Gypsophila pallasii, Haplophyllum suaveolens, Hedera helix, Helianthemum salicifolium, Helianthus annuus, Heliotropium europaeum, Helminthotheca echioides, Herniaria incana, Hordeum bulbosum, Hordeum murinum, Hypericum elegans, Hypericum perforatum, Inula ensifolia, Inula oculus-christi, Iris pumila, Iris sintenisii, Jasminum fruticans, Jurinea consanguinea subsp. arachnoidea, Koeleria lobata [syn. Koeleria brevis], Koeleria nitidula, Lactuca quercina, Lactuca serriola, Lactuca viminea s.l., Lamium amplexicaule, Lamium purpureum, Lathyrus cicera, Legousia speculum-veneris s.l., Leonurus cardiaca, Ligustrum vulgare, Limonium latifolium, Limonium meyeri, Linaria genistifolia, Linum austriacum, Lolium perenne, Lolium rigidum subsp. lepturoides, Malva sylvestris, Marrubium peregrinum, Medicago arabica, Medicago minima, Medicago rigidula, Medicago sativa subsp. falcata, Melica ciliata, Milium vernale, Minuartia bilykiana, Minuartia glomerata, Minuartia setacea, Morus alba, Muscari racemosum, Myagrum perfoliatum, Myosotis arvensis subsp. arvensis, Myrrhoides nodosa, Nectaroscordum siculum, Onopordum acanthium, Onosma heterophylla, Opopanax chironium subsp. bulgaricum, Orlaya grandiflora, Ornithogalum comosum, Paeonia peregrina, Paeonia tenuifolia, Paliurus spina-christi, Papaver rhoeas, Parapholis incurva, Parietaria lusitanica subsp. serbica, Parietaria officinalis, Petrorhagia prolifera [syn. Tunica prolifera], Phleum paniculatum, Phleum subulatum, Phragmites australis, Pimpinella peregrina, Pisum sativum subsp. elatius, Plumbago europaea, Poa bulbosa, Poa nemoralis, Polygonum aviculare, Potentilla recta, Potentilla taurica, Prunus cerasifera, Prunus mahaleb, Prunus spinosa, Psilurus incurvus, Puccinelia limosa, Pyrus communis, Quercus pubescens, Ranunculus ficaria, Reseda lutea, Rhus coriaria, Robinia pseudacacia, Rubus caesius, Rumex patientia, Rumex tuberosus, Ruscus aculeatus, Salsola kali subsp. ruthenica, Salvia amplexicaulis, Salvia austriaca, Salvia nemorosa, Salvia nutans, Sambucus ebulus, Sanguisorba minor s.l., Satureja caerulea, Saxifraga tridactylites, Scabiosa ochroleuca, Scandix australis, Scandix pecten-veneris s.l., Scorzonera mollis, Sedum caespitosum, Sedum maximum, Sedum sexangulare, Sedum urvillei subsp. hillebrandtii, Senecio vernalis, Senecio vulgaris, Seseli campestre, Seseli rigidum, Setaria verticillata, Setaria viridis, Sherardia arvensis, Sideritis montana, Silene latifolia subsp. alba, Silene bupleuroides, Silene caliacrae, Silene conica, Silene dichotoma, Silene exaltata, Silybum marianum, Sinapis arvensis, Sisymbrium officinale, Sisymbrium orientale, Solanum dulcamara, Solanum nigrum, Sonchus oleraceus, Spergularia media, Stellaria media s.l., Sternbergia colchiciflora, Stipa capillata, Stipa lessingiana, Tagetes patula, Tamus communis, Tanacetum corymbosum, Tanacetum millefolium, Taraxacum officinale, Taraxacum serotinum, Teucrium chamaedrys, Teucrium polium subsp. capitatum, Thesium dollineri, Thlaspi 27 perfoliatum, Thymus pannonicus, Thymus zygioides, Tordylium maximum, Torilis arvensis, Torilis nodosa, Tragopogon dubius, Tragus racemosus, Tribulus terrestris, Trifolium echinatum, Trigonella gladiata, Trigonella monspeliaca, Triticum aestivum, Ulmus minor, Urtica dioica, Valeriana officinalis, Valerianella pumila, Verbascum banaticum, Verbascum ovalifolium s.l., Verbascum phoeniceum, Verbena officinalis, Veronica austriaca subsp. austriaca [syn. Veronica jaquinii], Veronica hederifolia s.l., Veronica orchidea, Viburnum lantana, Vicia narbonensis, Vicia pannonica, Vicia peregrina, Vicia sativa subsp. nigra, Vinca herbacea, Vincetoxicum hirundinaria, Viola kitaibeliana, Vulpia myuros, Xanthium italicum, Xanthium spinosum, Xeranthemum annuum. Other 11 taxa are mentioned by literature (Kozhuharov et al., 1997; Kozhuharov et al., 2001) : Adonis volgensis, Anemone sylvestris, Carduus uncinatus, Centaurium turcicum, Erodium hoefftianum, Gypsophila perfoliata, Hypecoum ponticum, Ruta graveolens, Sideritis syriaca, Thalictrum aquilegiifolium s.l., Verbascum purpureum. These taxa belong to 62 families. Asteraceae prevails with 53 taxa (15.68%). This is followed by Poaceae with 40 taxa (11.83%), Caryophyllaceae with 21 taxa (6.21%), Lamiaceae with 19 taxa (5.62%), Brassicaceae with 17 taxa (5.02%), Fabaceae with 16 taxa (4.73%), Apiaceae with 15 taxa (4.43%), Rosaceae with 13 taxa (3.84%) and Scrophulariaceae with 10 taxa (2.95%) (Fig. 2). Other 30 families are represented by 9-2 taxa, while 24 families are represented by one taxa. Famil SCR ROS API FAB BRA LAM CAR POA AST 0 10 20 30 40 50 60 Number of species and subspecies Fig. 2 – Spectrum of the main plant families from Kamen Bryag – Yailata According to life forms, the flora from Kamen Bryag – Yailata has the following structure (Fig. 3): therophytes – 115 taxa (34.02%), hemicryptophytes – 108 taxa (31.95%), phanerophytes – 26 taxa (7.69%), geophytes – 23 taxa (6.80%), hemitherophytes – 23 taxa (6.80%), chamaephytes – 15 taxa (4.43%), therophytes– hemitherophytes – 13 taxa (3.84%), hemitherophytes–hemicryptophytes – 9 taxa (2.66%), hemicryptophytes– chamaephytes – 2 taxa (0.59%), therophytes - hemicryptophytes – 2 taxa (0.59%), chamaephyte–phanerophyte – 1 taxon (.29%), hemicryptophyte–geophyte – 1 taxon (0.29%). The high percent of therophytes is correlated with dry climate of this area, while the hemicryptophytes are characteristic for grasses communities, at Kamen Bryag – Yailata these dominating the limestone plateau. 28 T H Ph G Ht Ch T-Ht Ht-H H-Ch T-H Ch-Ph H-G Fig. 3 – Spectrum of life forms of flora from Kamen Bryag – Yailata Eur.centr. & SE As Pont.-pan. Eur.centr. Atl.-medit. Eur.centr.-submedit. Eur.centr.-medit. Geoeleme Circ. Pont. Pont.-pan.balc. Eur. Adv. Balc. Submedit. Cosm. Pont.-medit. Pont.-balc. Euras.cont. Medit. Euras. 0 10 20 30 40 50 60 70 Number of taxa Fig. 4 – Spectrum of the main geographic elements of flora from Kamen Bryag - Yailata The analysis of geographic elements of flora from Kamen Bryag – Yailata (Fig. 4) reveals the prevailing of Steppe elements (76 taxa – 22.48%): Ponto-Balkan – 29 taxa, Ponto-Mediterranean – 22 taxa, PontoPannonian-Balkan – 10 taxa, Pontic – 9 taxa, Ponto-Pannonian – 4 taxa, Ponto-Caucasian – 1 taxon, PontoMediterranean-Atlantic – 1 taxon. These are followed by Euro-Asian elements (63 taxa – 18.63%), Mediterranean – 39 (11.53%) and continental Euro-Asian elements (34 taxa – 10.05%). Sub-Mediterranean and Balkan elements are well represented too, with 16 taxa (4.73%) and, respectively, 14 taxa (4.14%). Among cosmopolite elements, we identified here 18 taxa (5.32%). Alien plants are represented by 13 taxa (3.84%), but they have only small populations, especially along the roads and pathways. According with Red Data Book of Bulgaria [Velchev (ed.), 1984], the following rare species were recorded to Kamen Bryag – Yailata: Adonis volgensis (Kozhuharov et al., 1997, Buglossoides arvensis subsp. sibthorpiana – sporadic on limestone plateau, Carduus uncinatus (Kozhuharov et al., 1997), Convolvulus lineatus – rare on limestone plateau, Crithmum maritimum – rare on rocky cliff, Ficus carica – frequent on rocky cliff, Goniolimon besserianum – sporadic on limestone plateau, Gypsophila perfoliata (Kozhuharov et al., 1997), 29 Hypecoum ponticum (Kozhuharov et al., 1997), Koeleria lobata – sporadic on limestone plateau, Onosma heterophylla – sporadic on limestone plateau, Opopanax chironium subsp. bulgaricum – frequent on cliff, Paeonia tenuifolia – sporadic on limestone plateau, Parapholis incurva – rare in grassland (43°26'33"N, 28°32'55"E), Scandix australis – frequent on limestone plateau, Sideritis syriaca (Kozhuharov et al., 1997), Silene caliacrae – rare on rocky cliff (43°27'11"N, 28°33'31"E), Stipa lessingiana – frequent on limestone plateau, Verbascum purpureum (Kozhuharov et al., 1997). To these we add four endangered species: Artemisia pedemontana – rare on limestone plateau, Limonium latifolium and Limonium meyeri – rare on rocky cliff, Ruta graveolens (Kozhuharov et al., 1997). Among the species listed in Biodiversity Law we recorded on Kamen Bryag – Yailata area: Paeonia tenuifolia – sporadic on limestone plateau, Artemisia pedemontana, Convolvulus lineatus, Galanthus elwesii – in a forest at SW of Kamen Bryag (43°25'35"N, 28°31'53"E), Goniolimon besserianum, Limonium latifolium, Limonium meyeri, Silene caliacrae – endemic species for this region. Paeonia tenuifolia is also strictly protected species according to Bern Convention. Among species listed in Habitat Directive, only Ruscus aculeatus grows here. Its harvesting from the wild is forbidden. The conservation status of all these plants is favourable, the threats being almost absent. Some inventoried plants to Kamen Bryag – Yailata are rare, although they are not included in Red Data Book of Bulgaria [Velchev (ed.), 1984]. They are represented here by only few individuals: Centaurea alba subsp. caliacrae – local endemic, on limestone plateau, Centaurea napulifera subsp. thirkei – Mediterranean element, rare on limestone plateau, Cynoglossum creticum – Mediterranean element, very rare on limestone plateau, Dianthus leptopetalus – Ponto-Balkan element, rare on limestone plateau, reported for the first time for this region, Fumaria kralikii – Mediterranean element, rare on rocky places, Parietaria lusitanica subsp. serbica – Ponto-Balkan element, rare on stony cliff, Nectaroscordum siculum – Ponto-Balkan element, very rare in forest, Pisum sativum subsp. elatius – Mediterranean species, rare in shrub formations at the border of forest, Salvia amplexicaulis – Daco-Balkan species, rare on stony grassland from the plateau. We also mention the presence of some alien species: Ailanthus altissima, Amaranthus crispus, Amaranthus retroflexus, Brassica juncea, Conyza canadensis, Datura stramonium, Gleditsia triacanthos, Morus alba, Robinia pseudacacia, Xanthium italicum, Xanthium spinosum. These are spread especially along roads and pathways and don’t seem to be a threat for the native flora. Occasionally Triticum aestivum, Helianthus annuus, Tagetes patula and Pyrus communis could be found as escaped from cultivation. Conclusions Taking into account the surface of researched territory (about 300 ha), we assert that the floristic diversity of Kamen Bryag – Yailata is high. Because our study was only a preliminary one, we suspect a higher number of taxa for this region. Thermophile plants are dominating here, many of them being at the northern limit of their distribution. Many rare plant species, protected at national or European level, occur to Kamen Bryag – Yailata having a favourable status and making this territory very important for conservation. References 1. 2. 3. 4. 5. ASSYOV B., Petrova A., 2006 – Conspectus of the Bulgarian Vascular Flora. Distribution maps and floristic elements, Bulgarian Biodiversity Foundation, Sofia, 453 pp. (in Bulgarian). BONDEV I., 1991 – The vegetation of Bulgaria. Map 1: 600 000 with explanatory text, St. Kliment Ochridski University Press, Sofia (in Bulgarian). CIOCÂRLAN V., 2000 – Illustrated flora of Romania. Pteridophyta et Spermatophyta, Publ. house Ceres, Bucureşti, 1140 pp. (in Romanian) GEORGIEVA N., Vladev D., 2007 – Geography of Bulgaria, Publ. House „Faber”, Veliko Tarnovo, 410 pp. (in Bulgarian). KITANOV B., Penev I., 1980 – Flora of Dobrudja, Publ. House “Nauka i izkustvo”, Sofia, 630 pp. (in Bulgarian). 30 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. 21. KOZHUHAROV S., Dimitrov D., Lazarova M. & Kozhuharova E. 1997 – Characterization of flora and vegetation of natural plant complexes in southern Dobrudja. In: Collection of papers “Dobrudja and Kaliakra”, HIA Academic Press, Plovdiv, Pp. 42-58 (in Bulgarian). KOZHUHAROV S., Dimitrov D., Kozhuharova E. & Lazarova M., 2001 – Notes of the flora of the rocky limestone coast near village Kamen Brjag (NE Bulgaria). OT Sist. Bot. Dergisi 8/1 & 15-27. PAN U Z., 1925 – Contribution to flora of New Dobrudja, Caliacra and Durostor counties, Publ. House “Cultura Na ional ”, Bucureşti, 127 pp. (in Romanian). PAŞCOVSCHI S., 1938 – Contribution to flora of Cadrilater, Revista P durilor 50(3): 241-248. (in Romanian). PRODAN I., 1935 – Conspectus of Dobrudja Flora, First part, Publ. House “Tipografia Na ional ”, Cluj, 170 pp., 62 plates. (in Romanian). PRODAN I., 1936 – Conspectus of Dobrudja Flora, Second part, Publ. House “Tipografia Na ional ”, Cluj, 57 pp. + 46 plates. (in Romanian). PRODAN I., 1939 – Conspectus of Dobrudja Flora, Third part, Publ. House “Tipografia Cartea Româneasc ”, Cluj, 96 pp., 30 plates. (in Romanian). TUTIN, T.G., Burges, N.A., Chater, A.O., Edmonson, J.R., Heywood, V.H., Moore, D.M., Valentine, D.H., Walters, S.M. & Webb, D.A. (eds., assist. by J.R. Akeroyd & M.E. Newton; appendices ed. By R.R. Mill), 1993 – Flora Europaea. 2nd ed. Vol. 1. Psilotaceae to Platanaceae. Cambridge University Press, Cambridge. TUTIN, T.G., Heywood, V.H., Burges, N.A., Moore, D.M., Valentine, D.H., Walters, S.M. & Webb, D.A. (ed.), 1964-1980 – Flora Europaea. Vols. 1-5. Cambridge University Press, Cambridge. VELCHEV V. (ed.) 1984. Red Data Book of the People's Republic of Bulgaria. Volume 1. Plants. Sofia: Publishing House of the Bulgarian Academy of Sciences (in Bulgarian). *** 1980 – Geomorphological map of Bulgaria, scale 1: 600000. Geographical institute of BAS, Geodesy and cartography office (in Bulgarian). *** 1982 – Geography of Bulgaria. Physical geography, BAS, Geographical Institute, 513 pp. (in Bulgarian). *** Biodiversity Law, promulgated in the State Gazette no. 77/9.08.2002 (in Bulgarian). *** The Bern Convention on the Conservation of the European Wildlife and Natural Habitats, Appendix I, 1979. *** Council Directive 92/43/EEC of 21 May 1992 on conservation of natural habitats and of wild fauna and flora, annex V. *** IUCN Red List of Threatened Species 2008 - http://www.iucnredlist.org Acknowledgments Many thanks to Ciprian Samoil , PhD student at University Ovidius Constan a, providing us with the map of the region Kamen Bryag – Yailata. The study was supported by the grant Phare CBC Ro 2005/017-535.01.02.02. 31 STUDY OF THE HIGHER FLORA ON THE TERRITORY OF KALIAKRA RESERVE Zheni NANOVA*, Marius F G RAŞ**, Paulina ANASTASIU***, Gavril NEGREAN*** * University of Shoumen, Faculty of Natural Sciences, str. "Universitetska" 115, Shoumen 9712, Bulgaria, E-Mail: jenidim@gmail.com ** Ovidius University of Constanţa, Faculty of Natural and Agricultural Sciences, Constanţa 900552, Romania *** University of Bucharest, Faculty of Biology, Department of Botany & Microbiology, Bucharest, 76900, Romania Abstract: field researches were carried out on the territory of Kaliakra reserve during the period April August 2008. The purpose of the study is: Inventory of taxonomic diversity, analysis of floristic elements and life forms, establishment of endemic taxa and conservation status of taxa. As a result of the study 351 species of higher plants, referring to 222 genera and 62 families were found. Most of the species relate to two phytogeographic areas - Eastern Mediterranean and steppe-Pontic. 45 species with conservation status were established on the territory of the reserve. Key words: taxonomic diversity, floristic elements, endemic plants, conservation status Introduction "Kaliakra" is declared for a National Park in 25.09.1941 in 1966 it is categorized as a reserve. In 4.04.1980 its territory was expended and included part of the marine strip. Its main purpose is the conservation of the primary steppe vegetation, some bird species and natural habitats of monk seal (Monachus monachus). The reserve is the only one in Bulgaria that includes a sea aquatory. The total area of the reserve is 687.5 ha (287.5 ha of land part and 400 ha sea part). Kaliakra belongs to a group of the protected territories in the country, category I - strict nature reserve. Kaliakra reserve is situated on the Cape Kaliakra and neighbouring aquatory. Cape Kaliakra is part of the eastern periphery of Dobrudja plateau and is included into the same name natural-geographic subregion of the Northern Black Sea coast. Cape Kaliakra is shaped into a well-developed rock ledge. In geological terms this territory is part of the Moesian platform (Georgieva et Vladev, 2007; Geography of Bulgaria, 1980). Here lower sarmatian clays, chalky sandstones and marls, middle sarmatian marly clays, chalky sandstones and sands and upper sarmatian shellfish limestone are disclosed (Soil map of Bulgaria, 1965). This is one of the most dangerous earthquake zones in Bulgaria with magnitude 7 (the highest of all regions). There is a serious danger of windstorms and lendslides throughout the region of Cape Kaliakra.The soils on the nose and in the surroundings are humus-calcareous type (Bondev, 1991). The reserve belongs to the Black Sea climatic region. The climate is temperate continental, but with significant humidity. It features relatively mild, humid winter and dry, hot summer. The average annual air temperature in Kaliakra is 11 . August is the hottest month with average monthly temperatures of 22,5 and the coolest month is January, with average monthly temperature 0.8 . The multi-annual total of rainfalls in the region is 450-500 mm with rainfall maximum in February. In recent years there has been a reduction in the amount of rainfall and climate in the region has become increasingly arid in nature. River flow is irregular due to thekarst terrain (Georgieva et Vladev, 2007; Geography of Bulgaria, 1980). The Kaliakra reserve occupies the eastern part of South Dobrudja, with vegetation belonging to the steppe and semisteppe communities (Delipavlov et al., 1969). In vegetation mainly grass phytocenoses dominates. The most frequent are found formations, with domination of cereals - Poa bulbosa, Agropyron sp., Koeleria sp. etc. 32 The formations of Stipa pennata and Stipa capillata are relatively widespread . Less distributed are the formations of Stipa lessingiana, Artemisia pedemontana and Artemisia pontica. Iris sp., Adonis sp. and Paeonia sp. develop together with cereal plants in spring. Achillea sp., Salvia sp., Thymus sp. etc. appear in June. Species diversity significantly reduced in August (Kozhukharov et al., 1979; Andreev et al., 1992). Material and Methods For establishing a floristic composition the route method was applied. The routes were matched so as to cover the most diverse habitats. Much of the identified locations were visited several times during the vegetation period of 2008 (at once in April, May, June, July and August), so the most complete inventory of species composition. The following indicators were assessed in the floristic analysis: number of taxa by category, the richest in species and genera families, the richest in species genera, biological spectrum, floristic elements, endemic species and taxa with conservation status. The determination of taxa were carried out with “Guide to the Vascular Plants in Bulgaria” (Andeev et al., 1992) and Flora of Bulgaria, volumes I-X (Yordanov (ed.), 1964-1995). The determination of floristic elements is on a basis of “Conspectus of the Bulgarian vascular flora. Distribution maps and floristic elements” (Assyov et al., 2006). The species with conservation status are associated with: Atlas of endemic plants in Bulgaria (Velchev et al., 1992); Red Book of P.R.Bulgaria, v. 1: Plants (Velchev (ed.), 1984); Biodiversity Law and Annex I of Bern Convention. Results and Discussion The flora of Kaliakra reserve includes 351 species of vascular plants, belonging to the 221 genera and 61 families (table 1). The established species constitute 9.84% of the flora of Bulgaria (3567 species) (Yordanov (ed.), 1964-1995) and 25.66% of the flora of Dobrudja (1368 species) (Kitanov, Penev, 1980). The families represented by the biggest number of species are : Asteraceae – 56, Poaceae – 38, Fabaceae – 25, Lamiaceae – 21, Brassicaceae – 19, Caryophyllaceae – 16, Boraginaceae – 15, Apiaceae – 11, Scrophullariaceae – 11, Liliaceae – 10, Rosaceae – 10. No. Tab. 1 - Established in the reserve families with number of genera and species Family Number of genera Number of species 1 Asteraceae 31 56 2 Poaceae 24 38 3 Fabaceae 14 25 4 Lamiaceae 12 21 5 Brassicaceae 13 19 6 Caryophyllaceae 9 16 7 Boraginaceae 10 15 8 Apiaceae 10 11 9 Scrophullariaceae 5 11 10 Liliaceae 6 10 11 Rosaceae 8 10 12 Rubiaceae 4 9 13 Ranunculaceae 7 8 33 14 Chenopodiaceae 5 7 15 Geraniaceae 2 7 16 Euphorbiaceae 2 6 17 Papaveraceae 3 6 18 Dipsaceaea 2 5 19 Convolvulaceae 2 4 20 Malvaceae 3 4 21 Plumbaginaceae 2 4 22 Polygonaceae 2 4 23 Linaceaea 1 3 24 Oleaceae 3 3 25 Asclepiadaceae 2 2 26 Crassulaceae 1 2 27 Cyperaceae 2 2 28 Hypericaceae 1 2 29 Orobanchceae 1 3 30 Plantaginaceae 1 2 31 Primulaceae 2 2 32 Rutaceae 2 2 33 Aspleniaceae 1 2 34 Salicaceae 1 2 35 Violaceae 1 2 36 Valerianaceae 1 2 37 Anacardiaceae 1 1 38 Apocinaceae 1 1 39 Araceae 1 1 40 Campanulaceae 1 1 41 Cannabaceae 1 1 42 Celastraceae 1 1 43 Cistaceae 1 1 44 Dioscoreaeceae 1 1 45 Eleagnaceae 1 1 46 Equisetaceae 1 1 47 Iridaceae 1 1 48 Lithraceae 1 1 34 49 Moraceae 1 1 50 Paeoniaceae 1 1 51 Resedaceae 1 1 52 Rhamnaceae 1 1 53 Saxifragaceae 1 1 54 Simaroubaceae 1 1 55 Solanaceae 1 1 56 Tamaricaceae 1 1 57 Thymelaeceae 1 1 58 Ulmaceae 1 1 59 Urticaceae 1 1 60 Verbenaceae 1 1 61 Vitaceae 1 1 Total 221 351 Figure 1 shows the ten largest families in the flora of Bulgaria (Angelova et al., 2006). The families in first three places on both figures are Asteraceae, Poaceae and Fabaceae. The biggest differences between two figures are the positions of families Lamiaceae and Rosaceae. The Lamiaceae, which is in the ninth position for the country moves up to the fourth place for the flora of Kaliakra. The presence of many species of family Lamiaceae is due to a specific geographical location of the research area, namely its proximity to the Eastern Mediterranean and Pontic phytogeographical centres (sources of species for this family). The fact that representatives of the Lamiaceae are mainly thermophytes and xerophytes and they are located in the appropriate environmental conditions in the research area is also important. The last fact is valid and for family Boraginaceae, which is in the seventh position in the flora of Kaliakra, but is not among the ten most numerous families of the Bulgarian flora. Number of species 500 400 300 200 100 0 1 2 3 4 5 6 7 8 9 10 Families Fig. 1 - The ten richest families in species in the flora of Bulgaria: 1-Asteraceae, 2-Poaceae, 3-Fabaceae, 4-Rosaceae, 5-Caryophyllaceae, 6-Brassicaceae, 7-Scrophulariaceae, 8-Apiaceae, 9-Lamiaceae, 10-Ranunculaceae 35 The Rosaceae, which is in the fourth position for Bulgaria, shares a tenth place with Liliaceae in flora of Kaliakra. Low representation of the family Rosaceae can be explained by the fact that the family is rich in species of Alpine and Boreal origin for which the environmental conditions in the territory of Kaliakra reserve are not appropriate. Family Ranunculaceae, which is ranks the tenth place for the country is not among the ten most numerous families in the flora of Kaliakra. This is due to the fact that much of the species of family Ranunculaceae are hygrophytes and mesophytes and the environmental conditions in the territory of the reserve do not advantage their development. The first five families richest in genera are the same five families which are richest in species (Fig. 2): Asteraceae – 31, Poaceae – 24, Fabaceae – 14, Brassicaceae – 13, Lamiaceae – 12. From the established genera richest in species are: Centaurea – 7, Astragalus – 6, Galium – 6, Veronica – 6, Bromus – 5, Euphorbia – 5, Geranium – 5, Allium – 4, Artemisia – 4, Vicia - 4. Number of species 60 50 40 30 20 10 0 1 2 3 9 6 5 11 8 7 12 4 Families Fig. 2 - The ten richest families in species in the flora of Kaliakra reserve: 1-Asteraceae, 2-Poaceae, 3-Fabaceae, 9-Lamiaceae, 6-Brassicaceae, 5-Caryophyllaceae, 11-Boraginaceae, 8-Apiaceae, 7-Scrophulariaceae, 12-Liliaceae, 4-Rosaceae According to their biological type the perennial herbaceous plants prevail in the flora of reserve - 168 species (47,86%); followed by annual herbaceous - 108 species (30,77%). The species in the next group are 28 (7,98%) and it includes: annual to biennial - 17, biennial to perennial – 4 and annual to perennial – 8. This group shares a third place with bushes and trees, also 28 species (7,98%) and the least of all are biennial - 15 species (4.27%). The floristic genetic analysis shows the following distribution of species in geoelements: 1. Euro-Asian - 60 species (17,09%) 2. Sub-Mediterranean - 49 species (13,96%) 3. Euro-Mediterranean - 47 species (13, 39%) 4. Pontic-Mediterranean - 30 species (8,55%) 5. Cosmopolites – 23 species (6, 55%) 6. Mediterranean - 21 species (5,98%) 7. Euro-Siberian – 16 species (4,56%) 8. European - 15 species (4,27%) 9. Pontic - 13 species (3,70%) 10. Mediterranean-Asian – 13 species (3,70%) 11. Balkan - 12 species (3, 42%) 36 12. Sub–Boreal – 9 species (2, 56%) 13. Boreal – 8 species (2, 28%) 14. Pontic- Asian - 8 species (2,28%) 15. Adventive – 5 species(1,42%) Generally, the species of different Mediterranean type of distribution (Sub-Mediterranean, Mediterranean, Euro-Mediterranean and Mediterranean- Asian) are 130, which constitute 37,04% of the total number of species on territory of reserve (Fig. 3). The site is the richest in steppe-Pontic species in Bulgaria. Their scope is related mainly to the EuroAsian, Euro-Siberian, Pontic-Mediterranean, Pontic, and Pontic-Asian geoelements. In the territory of the reserve, they are represented by a total of 127 species (36,18%) (Fig. 3). The environmental conditions in the reserve are not appropriate for Boreal floristic elements (Boreal and Sub-Boreal–4,84%), so they a represented lessthoroughly. On the territory of the reserve 45 plant species with conservation status are found (Tab. 2) - 15 species according to literary data (Delipavlov et al, 1979) and 30 according to our studies. Kaliakra Reserve is classified as relatively poor in endemic taxa. Established eleven endemic plants (11 Balkan and 1 Bulgarian), which constitute 3,42% of the total number of species on studied territory. From the endemic species, the largest population has Achillea clypeolata. Other endemic species are presented with smaller populations. Boreal Cos 5% 7% Others 7% Eur Balkan 3% 4% Med 38% St-Pont 36% Fig. 3 - Distributions of species in geoelements: Med - species of different Mediterranean type of distribution, St-Pont - steppe-Pontic species, Cos – Cosmopolites, Eur- Europian , Boreal – Boreal and sub-Boreal, Balkan – different Balkan geoelements Tab. 2 - Conservation status and endemism of plant species in Kaliakra reserve Species Achillea clypeolata Sibth. et Sm. Alyssum borzeanum Nyár. * Anemone sylvestris L. * Artemisia lerchiana Weber. * Artemisia pedemontana Balb. Artemisia pontica L. Astragalus cornutus Pall. Endemism, categories Red Book of Bulgaria, categories Biodiversity Law Annex, № Bern Convention 3 3 3 3 + Balkan Endangered Rare Endangered Rare Endangered 37 3 Astragalus spuneri Boiss. Asyneuma anthericoides (Janka) Bornm. * Aurinia uechtritziana (Bornm.) Cullen et T. R. Dudley * Bellevalia sarmatica (Pall.ex Gweorgi) Woronow Buglossoides arvensis (L.) I.M.Johnst. subsp. sibthorpiana (Griseb.) R.Fern. Chamaecytisus jankae (Vel.) Rothm. Centaurea arenaria M. Bieb. ex Willd. * Centaurea caliacrae Prod. Centaurea napulifera Rochel subsp. thirkei (Sch.Bip.) Dostál Centaurea varnensis Vel. Cerastium gracile Dufour [syn. Cerastium bulgaricum R.Uechtr.] * Cladium mariscus (L.) Pohl. Convolvulus lineatus L. Crambe tataria Sebeok * Erysimum bulgaricum (Vel.)Anchev ex Polatschec Ficus carica L. Geranium tuberosum L. Goniolimon besseranum (Schult. ex Rchb.) Kusn. Gypsophila perfoliata L. [syn. Gypsophyla trichotoma Wender] Iris suaveolens Boiss. & Reut. * Koeleria lobata (M.Bieb.) Roem. & Schult. [syn. Koeleria brevis Steven] Lactuca tatarica (L.) C.A.Mey Limonium latifolium (Sm.) O.Kuntze Limonium meyeri (Boiss.) O.Kuntze Matthiola odoratissima (Bieb.)R.Br. Nepeta ucrainica L. * Onosma heterophylla Griseb. Opopanax chironium (L.) W.D.J.Koch ssp. bulgaricum (Vel.) Andr. Orobanche essulae Panc. * Paeonia tenuifolia L. Potentilla emili-popii Nyár. * Ruta graveolens L. Scandix australis L. Sideritis syriaca L. * Silene caliacrae Jord. et Pan. * Stipa lessingiana Trin et Rupr. Typha shuttleworthii Koch et Sonder * Balkan Balkan Rare 2,3 + 3 Rare Balkan Rare 3 Balkan Balkan Balkan Rare Rare Rare Rare 3 3 3 Rare Rare Endangered 3 Rare 3 Balkan Balkan Rare Rare Endangered Endangered Endangered Rare Rare Rare 3 3 2, 3 2,3 3 Balkan Balkan Bulgarian 38 Endangered Rare Endangered Rare Endangered Rare Rare Rare 2, 3 2, 3 3 + + 3 3 + Vicia sativa L. subsp. amphicarpa (Dorthes) Asch. & Graebn. *according to the literary data [6] Endangered 3 Erysimum bulgaricum is a newly distinguished species for the Balkan Peninsula from M. Ancev and A. Polatschek (Ancev et al., 2003). Erysimum bulgaricum is found in the south-eastern and eastern parts of the Balkan Peninsula. In Bulgaria it is wide-spread in the South-East and East of the country in localities in the Upper Thracia plain, the Tundzha hilly region, along the Black Sea coast (Balchik, Kavarna, Kaliakra cape), in the East Stara Planina and in North-Eastern Bulgaria. Erysimum bulgaricum occurs in dry grassy habitats. Thirty-three plant species, from the flora of Kaliakra, are included in the "Red Book of Bulgaria” - 11 in the category "Endangered” and 22 in the category "Rare"; 24 species fall into annexes of Biodiversity Law. In the annex 1 of the Bern Convention five species are included. From these species with a few and small populations are: Astragalus cornutus, Belevallia sarmatica, Limonium latifolium, Limonium meyeri, Matthiola odoratissima, Gypsophila trichotoma, Ruta graveolens. Well shaped populations have Artemisia pontica, Ficus carica, Opopanax chironium subsp. bulgaricum, Paeonia tenuifolia, Stipa lessingiana. Conclusions In conclusion, the flora of Kaliakra, in the main part is made up of the species of two phytogeographic areas - Eastern Mediterranean and steppe-Pontic. Forty five endemic, rare, endangered and protected plant species with high conservation value can be find on territory of Kaliakra reserve. The primary steppe vegetation, which is distributed on such big area, cannot be found nowhere else in Bulgaria. It determines the territory’s exceptional conservation value. References ANCEV, M. and A. Polatschek, 2003 - Erysimum bulgaricum (Brassicaceae), a newly distinguished species for the Balkan Peninsula. Ann. Naturhist. Mus. Wien, 104 B: 691-698. 2. ANDREEV, N., M. Anchev, St. Kozhukharov, M. Marinova, D. Peev, A. Petrova, 1992 - Guide to the Vascular Plants in Bulgaria (in Bulgarian), Publ. House “Nauka i izkustvo”, Sofia, 788 pp. 3. ANGELOVA, K., K.Trendafilov, R.Petrova, 2006 - Floristic elements and systematic structure of the vascular flora of Vitosha floristic region (in Bulgarian). Scientific articles. Ecology, Part 1: 339-358. 4. ASSYOV, B., A. Petrova, D. Dimitrov, R. Vassilev, 2006 - Conspectus of the Bulgarian vascular flora. Distribution maps and floristic elements (in Bulgarian), Bulgarian biodiversity foundation, Sofia, 452 pp. 5. BONDEV, I., 1991 - The vegetation of Bulgaria. Map 1: 600 000 with explanatory text, (in Bulgarian), St. Kliment Ochridski University Press, Sofia. 6. DELIPAVLOV, D., D. Dimitrov, J. Guteva, Hr. Jancheva, 1979 - Flora and vegetation of Kaliakra Reserve and neighbouring territories. In: Collection of papers “Dobrudja and Kaliakra” (in Bulgarian), HIA Academic Press, Plovdiv, 27-35. 7. GEORGIEVA, N., D. Vladev, 2007 - Geography of Bulgaria (in Bulgarian), Publ. House “Faber”, Veliko Tarnovo, 410 pp. 8. Geography of Bulgaria. Physical geography (in Bulgarian), 1982. BAS, Geographical institute, 513 pp. Geomorphological map of Bulgaria, scale 1: 600 000. Geographical institute of BAS, Geodesy and cartography office, 1980. 9. JORDANOV, D. (Ed.), 1964-1995 - Flora of Bulgaria, volumes I-X (in Bulgarian), Publishing House of BAS. 10. KITANOV, B., I. Penev, 1980 - Flora of Dobruga (in Bulgarian), Publ. House “Nauka i izkustvo”, Sofia, 632 pp. 1. 39 11. KOZHUKHAROV, ST., D. Dimitrov, M. Lazarova, E. Kozhukharova, 1979 - Characterization of flora and vegetation of natural plant complexes in southern Dobrudja. In: Collection of papers “Dobrudja and Kaliakra” (in Bulgarian), HIA Academic Press, Plovdiv, 42-58. 12. VELCHEV, V., St. Kozhukharov, M. Anchev, 1992 - Atlas of endemic plants in Bulgaria (in Bulgarian), Publishing House of BAS, 205 pp. 13. VELCHEV, V. (Ed.), 1984 - Red Book of P.R.Bulgaria, v. 1: Plants (in Bulgarian), Publishing House of BAS, Sofia, 447 pp. 14. ***, 2002 - Biodiversity Law, promulgated in the State Gazette № 77, 9.08.2002. 15. ***, 1965 - Soil map of Bulgaria, scale 1:400 000, Geodesy and cartography head office. Annex I - Checklist of the plant species recorded from us of the Kaliakra Reserve Species Achillea clypeolata Achillea setacea Acinos rotundifolius Adonis flammea Adonis vernalis Aegilops cylindrica Aegilops neglecta [syn. Aegilops ovata] Agropyron cristatum ssp. pectinatum Agropyron cristatum subsp. ponticum Agrostis sp. Agrostis verticillatus Ailanthus altissima Ajuga chamaepytis Ajuga laxmannii Alcea rosea [syn. Althaea rosea] Alliaria petiolata Allium flavum subsp. tauricum Allium flavum subsp. flavum Allium moschatum Allium rotundum Allium saxatile Althaea cannabina Althaea hirsuta Alyssum caliacrae Alyssum desertorum Alyssum hirsutum Anagallis arvensis Anchusa arvensis [syn. Lycopsis arvensis] Anchusa stylosa Familia Asteraceae Asteraceae Lamiaceae Ranunculaceae Ranunculaceae Poaceae Poaceae Poaceae Poaceae Poaceae Poaceae Simaroubaceae Lamiaceae Lamiaceae Malvaceae Brassicaceae Liliaceae Liliaceae Liliaceae Liliaceae Liliaceae Malvaceae Malvaceae Brassicaceae Brassicaceae Brassicaceae Primulaceae Boraginaceae Boraginaceae 40 Floristic element Bal subMed Med-CAs Eur-subMed ur-Sib Eur-As subMed Eur-Pont Eur-Pont Eur-As Adv Pont-Med SSib Med Eur-as Med Med Pont-Med Eur-OT Med-As Med-As Pont-Med Pont subMed Cos Eur-Med subMed Biological type P P 1 P P 1 1 P P P T 1,2 P 2 1,2 M M P P P P P P 1 1 1,2 1 1 Androsace maxima Angelica sylvestris Anthemis austriaca Anthemis tinctoria Arabis recta [syn. Arabis auriculata] Arenaria serpyllifolia Artemisia absinthium Artemisia austriaca Artemisia pedemontana Artemisia pontica Arum orientale Asparagus verticillatus Asperula tenella Asphodeline lutea Asplenium adiantum-nigrum Asplenium trichomanes Aster oleifolius Astragalus cornutus Astragalus hamosus Astragalus monspessulanus Astragalus onobrychis Astragalus spruneri Astragalus varius [syn. Astragalus virgatus] Atriplex hastata Atriplex nitens Atriplex oblongifolia Avena barbata Avena clauda Bassia prostrata [syn. Kochia prostrata] Bellevalia sarmatica Beta trigyna Bombycilaena erecta Brachypodium pinnatum Brachypodium sylvaticum Brassica elongata Brassica juncea Brassica nigra Bromus hordeaceus Bromus japonicus Bromus squarrosus Bromus sterilis Bromus tectorum Primulaceae Apiaceae Asteraceae Asteraceae Brassicaceae Carryophyllaceae Asteraceae Asteraceae Asteraceae Asteraceae Araceae Liliaceae Rubiaceae Liliaceae Aspleniaceae Aspleniaceae Asteraceae Fabaceae Fabaceae Fabaceae Fabaceae Fabaceae Cos Pont-Sib Pont-As Eur-As Pont-Med Eur-As Bal Fabaceae Chenopodiaceae Chenopodiaceae Chenopodiaceae Poaceae Poaceae Chenopodiaceae Liliaceae Chenopodiaceae Asteraceae Poaceae Poaceae Brassicaceae Brassicaceae Brassicaceae Poaceae Poaceae Poaceae Poaceae Poaceae Pont-As Boreal Eur-As Eur-As Med-CAs Med-CAs Eur-as Pont Med Eur-Med SSib Eur-As Eur-as As Cos SMed Med-CAs subMed Boreal Boreal 41 Eur-As Eur-Sib Eur-Med Eur-Sib Eur-As Eur-As Pont-Med Eur-Sib Pont-Med Pont Med Pont-As subMed Pont-Med 1 2 1,2 P 1 1,2 P P P P P P P P P P P P P P P P P 1 1 1 1 1 B P P 1 P P 2, P 1 1 1-P 1 1 1 1 Buglossoides arvensis subsp. sibthorpiana Buglossoides purpurocaerulea Calystegia sepium Camelina microcarpa Camelina rumelica Campanula sibirica Capsella bursa-pastoris Cardaria draba subsp. draba Carduus pycnocephalus Carduus thoermeri Carex michelii Carthamus lanatus Celtis australis Centaurea caliacrae Centaurea diffusa Centaurea napulifera subsp. thirkei Centaurea salonitana Centaurea solstitialis Centaurea varnensis Cephalaria transylvanica Cephalaria uralensis Cerastium pumilum Cerastium glomeratum Ceratocephalus testiculatus Cerinthe minor susbsp. auriculata Chamaecytissus jankae Chenopodium album Cichorium intybus Cirsium vulgare Cladium mariscus Clematis vitalba Clypeola jonthlaspi Conium maculatum Consolida regalis Convolvulus arvensis Convolvulus cantabrica Convolvulus lineatus Conyza canadensis Coronilla scorpioides Coronilla varia Crataegus monogyna Crepis foetida subsp. rhoeadifolia Crepis sancta Boraginaceae Boraginaceae Convolvulaceae Brassicaceae Brassicaceae Campanulaceae Brassicaceae Brassicaceae Asteraceae Asteraceae Cyperaceae Asteraceae Ulmaceae Asteraceae Asteraceae Asteraceae Asteraceae Asteraceae Asteraceae Dipsacaceae Dipsaceae Caryophyllaceae Caryophyllaceae Ranunculaceae Boraginaceae Fabaceae Chenopodiaceae Asteraceae Asteraceae Cyperaceae Ranunculaceae Brassicaceae Apiaceae Ranunculaceae Convolvulaceae Convolvulaceae Convolvulaceae Asteraceae Fabaceae Fabaceae Rosaceae Asteraceae Asteraceae 42 Euro-As Eur-As Cos Pont-CAs Pont-CAs subMed Cos Eur-Med Med Pont-Pann-Bal Eur subMed Med Bal Pont-Med Pann-Bal Pont-Med Eur-Med Bal Pont-Med Pont-Med Eur-Med Cos Eur-As Pont-Med Bal Cos Eur-Sib Eur-Med Kos Eur Med Eur-As Eur-Med Cos Pont Eur-As NAm(Adv) subMed Eur-Med subBoreal Eur-Med subMed 1 P P 1,2 1,2 2 1,2 P 1 1 P 1 T 1 2 1- P P 1 2 1 P 1,2 1 1 1-P B 1 P 2 P B 1 1 1 P P P 1 1 P B, T 1 1 Cruciata pedemontana Crupina vulgaris Cynanchum acutum Cynodon dactylon Cynoglossum creticum Dactylis glomerata Daucus carota subsp. carota Dianthus leptopetalus Dianthus pseudarmeria Digitalis lanata Echinochloa crus-gallii Echinops exaltatus Echinops ritro subsp. ruthenicus Echinops sphaerocephalus Echium italicum Echium vulgare Elaeagnus angustifolius Elymus elongatus [syn. Agropyron] Elymus repens Equisetum telmateia Erodium ciconium Erodium cicutarium Erophila verna Eryngium campestre Erysimum bulgaricum Erysimum diffusum Euonymus europaeus Eupatorium cannabinum Euphorbia agraria Euphorbia helioscopia Euphorbia myrsinites Euphorbia nicaeensis s.l. Euphorbia nicaeensis subsp.dobrogensis Falcaria vulgaris Festuca valesiaca Ficus carica Filipendula vulgaris Fragaria viridis Fraxinus ornus Fumaria rostellata Fumaria officinalis Fumaria schleicheri Galega officinalis Rubiaceae Asteraceae Asclepiadaceae Poaceae Boraginaceae Poaceae Apiaceae Caryophyllaceae Caryophyllaceae Scrophulariaceae Poaceae Asteraceae Asteraceae Asteraceae Boraginaceae Boraginaceae Eleagnaceae Poaceae Poaceae Equisetaceae Geraniaceae Geraniaceae Brassicaceae Apiaceae Brassicaceae Brassicaceae Celastraceae Asteraceae Euphorbiaceae Euphorbiaceae Euphorbiaceae Euphorbiaceae Euphorbiaceae Apiaceae Poaceae Moraceae Rosaceae Rosaceae Oleaceae Papaveraceae Papaveraceae Papaveraceae Fabaceae 43 Med-CAs subMed Med-CAs Cos Med-CAs Eur-As Eur-As Med subMed Cos Eur Eur-Sib Eur-Med subMed Eur-As Adv Pont-SMed Boreal Boreal subMed subBoreal Eur-Med-Cas Pont-Med Bal CSEur Eur-As Eur-As subMed Eur-As subMed Eur-Med Eur-Med Eur-As Pont Med(Adv) Euro-Med Eur-Sib subMed Eur-Med Eur-Med Eur-As Pont-Med 1 2 B P 1,2 P 1 P 1 1,2 1 P P P 2 2 B P P P 1,2 1 1 P P 2, P B, T P P 1 P P P 1-P P B, T P P D 1 1 1 P Galium album subsp. pycnotrichum Galium aparine Galium flavescens Galium glaucum Galium humifusum Galium verum subsp. verum Geranium columbinum Geranium dissectum Geranium molle Geranium rotundifolium Geranium tuberosum Glaucium corniculatum Goniolimon besserianum Gypsophila perfoliata (G. trichotoma) Gypsophila palasii (G. glomerata) Haplophyllum suaveolens Helianthemum salicifolium Heliotropium europaeum Herniaria incana Hordeum bulbosum Hordeum murinum Humulus lupulus Hypericum elegans Hypericum perforatum Inula oculus-christi Iris pumila Jasminum fruticans Jurinea consanguinea subsp.arachnoidea Kickxia elatine Koeleria lobata (K. brevis) Koeleria nitidula Koeleria splendens Lactuca tatarica Lactuca viminea Lamium amplexicaule Lamium purpureum Lappula patula (syn.L.marginata) Lathyrus cicera Lembotropis nigricans Leontodon crispus Leontodon hispidus Ligustrum vulgare Limonium latifolium Rubiaceae Rubiaceae Rubiaceae Rubiaceae Rubiaceae Rubiaceae Geraniaceae Geraniaceae Geraniaceae Geraniaceae Geraniaceae Papaveraceae Plumbaginaceae Caryophyllaceae Caryophyllaceae Rutaceae Cistaceae Boraginaceae Caryophyllaceae Poaceae Poaceae Cannabaceae Hypericaceae Hypericaceae Asteraceae Iridaceae Oleaceae Asteraceae Scrophulariaceae Poaceae Poaceae Poaceae Asteraceae Asteraceae Lamiaceae Lamiaceae Boraginaceae Fabaceae Fabaceae Asteraceae Asteraceae Oleaceae Plumbaginaceae 44 Eur-As Eur-As Bal-Dac subMed Eur-Med Eur-As subMed Eur-As Eur-Med Eur-As subMed Eur-As Pont Eur-As subMed Med subMed Eur-As Eur-Med Eur-As Boeal Eur-Sib Eur-Sib Cos Eur-Med subMed Pont-CAs subMed-Sib subMed Pont-Med Pont Pont-Med Pont-As Eur-Med Eur-As Eur-Med Eur-As subMed Eur-Med Pont-Med Eur-Med subMed Pont P 1 P P P P 1 1 1,2 1 P 1,2 P P P P 1 1 1 P 1 P P P P P B P 1 P P P P 1 1 1 1 1 B P P B P Limonium meyeri Linaria genistifolia Linum austriacum Linum tauricum Linum tenuifolium Lolium perenne Lotus corniculatus Lycopus europaeus Lythrum salicaria Malva sylvestris Marrubium peregrinum Marrubium vulgare Matricaria perforata Matthiola odoratissima Medicago minima Medicago sativa subsp. falcata Melica ciliata Melilotus alba Mentha longifolia Mercurialis annua Milium vernale Minuartia sp. Minuartia glomerata Minuartia setacea Muscari racemosum Myosotis arvensis subsp. arvensis Myosotis stricta Nigella arvensis Nonea pulla subsp. atra Onobrychis gracilis Ononis pusilla Onopordum acanthium Onopordum tauricum Onosma heterophylla Onosma taurica Opopanax chironium ssp.bulgaricum Ornithogalum comosum Ornithogalum refractum Orobanche caryophyllaceae on Galium aparine Plumbaginaceae Scrophulariaceae Linaceae Linaceae Linaceae Poaceae Fabaceae Lamiaceae Lithraceae Malvaceae Lamiaceae Lamiaceae Asteraceae Brassicaceae Fabaceae Fabaceae Poaceae Fabaceae Lamiaceae Euphorbiaceae Poaceae Caryophyllaceae Caryophyllaceae Caryophyllaceae Liliaceae Boraginaceae Boraginaceae Ranunculaceae Boraginaceae Fabaceae Fabaceae Asteraceae Asteraceae Boraginaceae Boraginaceae Apiaceae Liliaceae Liliaceae Pont-CAs Pont-Sib subMed Pont-Med Pont-Med Eur-As Eur-Med Eur-As subBoreal Cos subMed Eur-As Eur-Med Pont-Med Eur-As Cas(Adv) Eur-subMed subBoreal Eur-Sib subMed subMed Orobanchaceae Eur Orobanche sp. on Achillea Orobanche sp. on Thymus Paeonia tenuifolia Orobanchaceae Orobanchaceae Paeoniaceae 45 Eur-Med Pont subMed Eur-As subMed subMed Pont-Med subMed Eur-Med Med subMed subMed Med Med subMed P 1 P P P P P P P P P P 1 P 1 P P 1 P 1 1 1- P P P 2 1 1 1 P P 1 1 P P P P P P P subMed P P Paliurus spina-christi Papaver hybridum Papaver rhoeas Parietaria officinalis Periploca graeca Petrorhagia prolifera [ Tunica prolifera] Phleum subulatum Phragmites australis Picris hieracioides Plantago lanceolata Plantago major Plumbago europaea Poa angustifolia Poa bulbosa Polygonum aviculare Populus alba Populus canescens Potentilla recta Potentilla pedata Prunus mahaleb Psilurus incurvus Pulicaria dysenterica Pyrus elaeagrifolia Ranunculus oxyspermus Reseda lutea Rhus coriaria Rosa sp. -1 Rosa sp.- 2 Rumex obtusifolius Rumex patientia Rumex tuberosus Ruta graveolens Salsola kali subsp. ruthenica Salvia aethiopis Salvia austriaca Salvia nemorosa Salvia nutans Sanguisorba minor Satureja coerulea Saxifraga tridactylites Scabiosa argentea Scabiosa micrantha Scabiosa ochroleuca Rhamnaceae Papaveraceae Papaveraceae Urticaceae Asclepiadaceae Caryophyllaceae Poaceae Poaceae Asteraceae Plantaginaceae Plantaginaceae Plumbaginaceae Poaceae Poaceae Polygonaceae Salicaceae Salicaceae Rosaceae Rosaceae Rosaceae Poaceae Asteraceae Rosaceae Ranunculaceae Resedaceae Anacardiaceae Rosaceae Rosaceae Polygonaceae Polygonaceae Polygonaceae Rutaceae Chenopodiaceae Lamiaceae Lamiaceae Lamiaceae Lamiaceae Rosaceae Lamiaceae Saxifragaceae Dipsaceae Dipsaceae Dipsaceae 46 Eur-As Med-CAs Eur-Sib Eur Pont-Med Pont-Med Eur-As Cos Eur-As Cos Boreal subMed Cos Eur-As Cos Eur-As Eur-Med subBoreal Med Eur-Med subMed Eur-Med Med Med-CAs subBoreal Med-As Eur-Med Eur-As Boreal Pont-Med Eur-As Eur-As Eur Eur-OT Eur-Sib subBoreal subMed subBoreal Bal-Anat Pont-Med Eur-Sib B, T 1 1 P B 1 1 P 1- P P P P P P 1 T T P P B, T 2 2 T P 1, P B B B P P P P 1 2, P P P P P B 1 1- P 1 2, P Scandix australis Scandix pecten-veneris Scorzonera hispanica Scorzonera laciniata Scorzonera mollis Sedum sp. Sedum urvillei subsp. hillebrandtii (syn.S.sartorianum) Senecio vernalis Seseli tortuosum Setaria verticillata Sherardia arvensis Sideritis montana Silene conica s.l. Silene dichotoma Silene exaltata Sisymbrium orientale Solanum nigrum Sonchus arvensis Sonchus oleraceus Spartium junceum Spergularia media Stachys recta Stachys atherocalyx Stipa capillata Stipa pennata Stipa lessingiana Tamarix ramosissima Tamus communis Tanacetum corymbosum Tanacetum millefolium Taraxacum erythropsermum Taraxacum officinale Taraxacum serotinum Teucrium chamaedrys Teucrium polium subsp. capitatum Thalictrum minus Taeniatherum caput-medusae Thlaspi perfoliatum Thymelaea passerina Thymus pannonicus Thymus zygioides Torilis nodosa Apiaceae Apiaceae Asteraceae Asteraceae Asteraceae Crassulaceae Eur-Med Eur-As Med Med Med Crassulaceae Asteraceae Apiaceae Poaceae Rubiaceae Lamiaceae Caryophyllaceae Caryophyllaceae Caryophyllaceae Brassicaceae Solanaceae Asteraceae Asteraceae Fabaceae Caryophyllaceae Lamiaceae Lamiaceae Poaceae Poaceae Poaceae Tamaricaceae Dioscoreaeceae Asteraceae Asteraceae Asteraceae Asteraceae Asteraceae Lamiaceae Lamiaceae Ranunculaceae Poaceae Brassicaceae Thymelaeaceae Lamiaceae Lamiaceae Apiaceae Eur Eur-Med subMed Cos Med subMed subMed-as Eur-Med 47 Eur-As Cos Eur-As Cos Med(Adv) Eur-As Eur-Med Pont-Med Pont-Med Eur Eur-As Eur-As subMed Eur-Med Pont Eur Eur-Med Pont Eur-Med Pont-Med Eur-Sib Eur-As Eur-Med Pont Eur subMed Eur-As 1 1 P P P P P 1 1,2 1 1 1 1 1,2 P 1,2 1 P 1 B P P P P P P B P P P P P P P P P 1 1 1 P P 1 Tragopogon dubius Trigonella gladiata Trigonella monspeliaca Tussilago farfara Valerianella carinata Valerianella pumila Verbascum banaticum Verbascum ovalifolium Verbena officinalis Veronica arvensis Veronica austriaca subsp. austriaca Veronica hederifolia Veronica polita Veronica prostrata Veronica spicata subsp. prodanii Vicia sativa subsp. amphicarpa Vicia pannonica Vicia peregrina Vicia sativa subsp. nigra Vinca herbacea Viola arvensis Viola kitaibeliana Vitis sylvestris Vulpia myuros Xanthium spinosum Xeranthemum annuum Asteraceae Fabaceae Fabaceae Asteraceae Valerianaceae Valerianaceae Scrophulariaceae Scrophulariaceae Verbenaceae Scrophulariaceae Scrophulariaceae Scrophulariaceae Scrophulariaceae Scrophulariaceae Scrophulariaceae Fabaceae Fabaceae Fabaceae Fabaceae Apocinaceae Violaceae Violaceae Vitaceae Poaceae Asteraceae Asteraceae 1 - annual herbaceous plant 2 - biennial herbaceous plant P - perennial herbaceous plant B - bush T - tree 48 Eur-Med subMed subMed Eur-As Eur-Med Pont-Med Bal-Dac Pont-Bal Cos Eur-Sib Eur-Med Eur-Med Eur-As Eur Pont Med Eur-Med Eur-As Eur-Med Eur-Med Eur Eur-Med subMed subBoreal Cos subMed 2 1 1 P 1 1 2 2 P 1 P 1 P P P 1 1 1 1 P 1 1 B 1 1 1 ROMANIAN BOTANICAL CONTRIBUTIONS TO THE STUDIES OF FLORA IN BULGARIAN DOBROGEA Gavril NEGREAN University of Bucharest, Botanical Garden, Cotroceni Str., No. 32, Bucharest, Romania negrean_gavril@yahoo.com __________________________________________________________________________________________ Abstract: Since the Bulgarian botanists do not know the botanic research that Romanian botanists made in Bulgarian Dobrogea we consider that it is appropiate to make them known. A short history of botany in Dobrogea is given. Also the authors’ contribution to the Flora and Mycobiota of Bulgaria. A list of taxa (Tracheophyta and Fungi) described by romanian botanists and over than 160 number of bibliography is added. Keywords: Botanical history, Bulgarian Dobrogea, described taxa, bibliography; __________________________________________________________________________________________ Introduction Since the Bulgarian botanists do not know the botanic research that Romanian botanists made in Bulgarian Dobrogea we consider that it is appropiate to make them known. The oldest knowledge over plants in Dobrogea had the people that had lived on these places from ancient times. Plants have been used in economical purpose, for food, clothing, constructions, remedies for illnesses etc. It is known that Dioskurides, one of the greatest doctors of antiquity, had left us as inheritance several hundreds of plants, described and even illustrated. A number of over 60 of them would be of Dacian origin. Over the dacian names of Dioskurides plants there been made botanic research but most with contradictory results. This is also due to the fact that lots copies after Dioskurides work had been done in the middle ages with lots of adding’s during the years. Recently, Constantin Dr gulescu from Sibiu University has issued a very interesting and bold hypothesis, that is: it is probably that Dioskurides himself, it some of its students, have flowed the roman armies trough Dobrogea, thus being possible that some names of plants to have been picked up by the students from the local peoples. Dr gulescu is identifyind even a number of approximately 20 plants that would exist also in Dobrogea, from Dioskurides’ lists. It is a very interesting hypothesis that makes as meditates. Another information regarding Dobrogea would be represented by the metopes from Adam-Klissi. This monument has been built by the Romans to celebrate the victory of the roman armies over the gethic people. On this metopes there are figured also several plants. Their analysis leads to the conclusion that eventual the architects that buolt this monuments were from southern origin and did not know well the areas around the monument. While the Trajan’s Column (from Rom, with a very good copy at the archeology Museum in Bucharest) brought up surprisingly results, through the meaning that the architect that accompanied Traian had seen plants from Transilvania and had eternalized them of thew Column. This is the case of the fir tree, which seems that 2000 years ago had not been known by the Romans and they would have known it on these places. Another very interesting aspect on naturalistic point of view is the fact that the Column it is figured a scene in which a delegation sent by Dekebal to Trajan was carrying a message written on a huge mushrooms (a Polyporaceae, after the pores can by seen it). On the mosaic discovered in Constan a there figured several plants, though they are very stylized and do not have much of a great for the histors of botanics from Dobrogea. Maybe only an aesthetic one. Some hints to the vegetation in Dobrogea the great poet Ovidius is also making in its writings. In the 17 century the great Turkish traveler Evvia Celebi is signaling in its travels through Dobrogea a plant, Prunus spinosa and says that he has been impressed by the fact that up north to Mangalia the „porumbes were as big as plums in Turkey” (Dobrogeanu, 1913). 49 The first Romanian botanic research have started after the year 1914 an have continued until today. The greatest explorer of entire Dobrogea has been Iuliu Prodan who even wrote a monograph very valuable over the province. Among other botanists that had researched Bulgarin Dobrogea we enumerate I. C. Constantineanu (the first in IX 1914), Zaharia Pan u, Alexandru Borza, Traian S vulescu and collaborators, Iuliu Nyárády, Emil Pop and others. We mention that the International Phytogeographic trip orgnized in the year 1931 in Romania had as objective also a few areas from Bulgarian Dobrogea. Thus we have large lists of plants from Caliacra Cape and even from the Ceracman Collin (Borza, 1931). Discussions What is my connection to the flora from Balcanic Peninsula and from Bulgaria? Exactly 60 years ago, my natural sciences professor Paul Pteancu, has tought me botanics in high school. He had been the best student of Alexandru Borza, one of the gretest Romanian botanists. Paul Pteancu had been sent to the Romania high school in Sofija to teach there natural sciences an expecially to familiarize with the Balcanic Peninsula flora because proferssor Borza was the adept of the postglaciary migrations towards the Carpathians of the flora an wanted to prepare his student for continouing the grounding of this theory. We ourselses have made botanic and mycologic researches through Bulgaria starting the year 1973 when had particpated to the first Flora anf Vegetation Congress of the Balcan Peninsula, held in Varna. Wee had then one of the greatest botanist of Europe: T. G. Tutin, J. Jalas, H. Meusel, A. L. Takhdadjean, G. Fekete, Sz. Priszter, J. Holub, S. M. Walters, C. Zahariadi, A. Strid, F. Ehrendorfer, W. Greuter and others. With that occasion I have visited also the Botanical Garden in Balcic, Caliacra Cape and have climbed on the „White hill” from Balcic, frecvent pinted from many romanian painters (Şirato, Tonitza, Petraşcu, D r scu, Iser etc.). With the occassion of Botanical Congress from Varna I have made botanical trips highly attractive, from Varna to Sofija (Mount Emine, Ajtos, Sliven, Stara-Zagora, Bacicovo, Plovdiv, Velingrad, Borovecz, Assenovgrad, Pirin and Rhodopi Mountains etc.). Starting the year 1997 I have had even an official collaboration with several Bulgarian botanists and mycologists among which Cvetomir Denchev, Sharkova, Gussev etc. I have collaborated with them on mycologic researches on some groups of fungus on the Bulgarian and Romanian coasts of Dobrogea (Peronosporales, Erysiphaceae, Uredina-les, Ustilaginales) I have visited then many interes-ting areas from eastern Bulgaria, environs of Balcic, from Ecrene to Duranculac, then towards south: Emine Cape, Burgas, Strandja Mountains etc. Several notes have been publisched by us with highly interesting results. Several plants and fungi have been distributed in the exsiccatae: Flora Romaniae Exsiccata and Herbarium Mycologicum Romanicum. Outnumbered taxons have been described all this time from Bulgarian Dobrogea (species and varieties). Among the more special species we mention: Agropyron bazargicensis Prodan, Agropyron sablensis Prodan, Alyssum caliacrae Nyár. (Bolata Dere), Astragalus nyaradyanus Prodan (Cavarna), Bromus dobrogensis Prodan (Cavarna), Bromus scoparius L. subsp. cavarnae Prodan, Centaurea caliacrae Prodan, Crambe dionisopolysi Prodan (Balcic), Crambe tataria Sebeok subsp. cavarnae Prodan, Cyclamen durostoricum Pan u & Solacolu Dianthus borzaeanus Prodan, Dianthus campestris Bieb. subsp. serbanii Prodan Dianthus dobrogensis Prodan, Euphorbia bazargica Prodan, 50 Euphorbia cadrilateri Prodan, Euphorbia dobrogensis Prodan, Festuca media Prodan (Balcic), Onosma ponticum Prodan (Balcic), Poa romanica Prodan (Simionova), Potentilla bazargica Prodan, Potentilla cavarnana Prodan, Potentilla emilii-popii Nyár. Stachys leucoglossa Griseb. ssp. caliacrae Prodan, Stachys patula Griseb. subsp. ajugaefolia Prodan. And countless variety and forms. Also some fungus: Calospora crataegi S vul. & Sandu, Cercospora psoraleae-bituminosae S vul. & Sandu, Cucurbitaria pontica S vul. & Sandu, Puccinia dob-rogensis S vul., Uromyces trifolii-purpurei Const. References 1. BONTEA Vera & CONSTANTINESCU O. 1968. Herbarium Mycologicum Romanicum “Tr. S vulescu”. Schedae. Fasc. I-XIX (nr. 1-950). Bucureşti. pp.: i-iv + 1-481. 2. BONTEA Vera & CONSTANTINESCU O. 1968. Herbarium Mycologicum Romanicum “Tr. S vulescu”. Schedae. Fasc. XX-XXXV (nr. 951-1750). Bucureşti. pp.: i-ii + 482-957. 3. BORZA Al. 1921. Bibliographia botanica Romaniae; annorum 1914-1920. Bul. Gr d. Bot. Cluj 1(2): 41-54. 4. BORZA Al. 1921. Bibliographia botanica Romaniae anni 1921 cum nonnulis additamen-tis ad bibliographiam annorum 1914-1920. Bul. Gr d. Bot. Cluj 1(3): 87-91. 5. BORZA A. 1922. Bibliographia botanica Romaniae. Bul. Gr d. Bot. Cluj 2(2): 62-64. 6. BORZA A. 1922. Bibliographia botanica Romaniae. Bul. Gr d. Bot. Cluj 2(3): 89-92. 7. BORZA A. 1925. Schedae ad "Floram Romaniae Exsiccatam". Cent. VI. (nr. 501-600). Bul. Gr d. Bot. Cluj 5(3-4): 81-102. 8. BORZA Al. 1927. Schedae ad "Floram Romaniae Exsiccatam". Cent. VII. (nr. 601-700 + Addenda). Bul. Gr d. Bot. Cluj 6(3-4): 81-102. 9. BORZA A. 1928. Flora Coastei de Argint la Cluj ● Flora of the Silver coast in Cluj. “Cartea M rii” Balcic 11 pp. 2 fig. 10. BORZA A. 1929. Schedae ad "Floram Romaniae Exsiccatam". Cent. VIII-IX. (nr. 701-900). Bul. Gr d. Bot. Cluj 8(2-4): 96-151. 11. BORZA Al. 1930. Problema protec iunei naturii în România ● The problem of the protection of la nature in Roumania. Pp. 94-127, pl. II-IX, 32 fig., 1 hart . In: A. BORZA & E. POP (red.), Întâiul Congres Naţional al naturaliştilor din România, ţinut la Cluj dela 18 pân la 21 aprilie 1928. Cluj, 1930. 12. BORZA A. 1931. (red.). Guide de la sixième excursion Phytogeographique interna-tionale, Roumanie. Cluj, 243 pp. 13. BORZA A. 1931. I. Partie. Die Vegetation und Flora Rumäniens. Pp.1-55. In: A. BORZA (red.), Guide de la sixième excursion Phyto-geographique internationale, Roumanie. Cluj: Minerva, 243 pp. + 18 Pl. + 1 charta. 14. BORZA A. 1931. IX. Partie. Die Excursi-onrute durch die Dobrogea und das Donaudelta. Pp. 130-144. In: A. BORZA (red.), Guide de la sixième excursion Phytogeographique interna-tionale, Roumanie. Cluj: Minerva, 243 pp. + 18 Pl. + 1 charta color. 15. BORZA A. 1931. Schedae ad “Floram Roma-niae exsiccatam”. Cent. X (No. 901-1000). Bul. Gr d. Bot. Cluj, 1930, 11(1-2): 1-26. 51 16. BORZA A. 1933. Schedae ad “Floram Romaniae exsiccatam”. Cent. XI (No. 1001-1100). Bul. Gr d. Bot. Cluj, 1932, 12(3-4): 117-158. 17. BORZA Al. 1933. Monumentele naturii în România. Boabe de Grâu anul IV, nr. 2(febr. 1933): 65-83. 18. BORZA A. 1934. Despre Artemisia caucasica, cu observa iuni critice asupra artemisiilor alpine eurasiatice - Artemisia caucasica nebst kritischen Bemerkungen über eurasiatische Hochgebirgsartemisien. Bul. Gr d. Bot. Cluj, 1933, 13(1-4): 20-46 + 5 pl. 19. BORZA A. 1936. Schedae ad “Floram Romaniae Exsiccatam”, Cent. XII-XIV (No. 1101-1400). Bul. Gr d. Bot. Cluj, 15(1-4): 1-64. 20. BORZA Al. 1937. Gr dinile Balcicului. Notiţe dela Gr d. Bot Cluj No. 18: 1-6. /extras din “Gr dina Mea” 3(7, 8, 9, 1937)/. 21. BORZA Al. 1937. Schedae ad “Floram Romaniae exsiccatam”. Cent. XV-XVI (No. 1401-1600). Bul. Gr d. Bot. Cluj, 1936, 16(1-4): 102-142. 22. BORZA A. 24 XII 1938. Schedae ad “Floram Romaniae exsiccatam”. Cent. XVII-XVIII (No. 16011800). Bul. Gr d. Bot. Cluj, 1938, 18(1-4): 20-64. 23. BORZA A. 1939. Dela Balcic la Oradea. Note botanice-horticole ● From Balcic to Oradea. BotanicHorticole Notes. Gr dina mea 5(3-4): 3-7. 24. BORZA A. 1939. Dela Balcic la Oradea. Note botanice-horticole ● From Balcic to Oradea. BotanicHorticole Notes. Notiţe dela Gr d. Bot. Cluj No. 34: 1-4. 25. BORZA A. 1940. O Clypeola nou pentru flora României. (Une Clypeole nouvelle pour la flore de la Roumanie). Bul. Gr d. Bot. Cluj 20(1-2): 1-7. 26. BORZA A. 1940. Schedae ad “Floram Romaniae exsiccatam”. Cent. XIX-XXI (No. 1801-2100). Bul. Gr d. Bot. Cluj, 1938, 20(1-2): 8-73. 27. BORZA Al. 1941. Schedae ad “Floram Romaniae exsiccatam”. Cent. XXII-XXIII (No. 2101-2300). Bul. Gr d. Bot. Cluj, 21(3-4): 82-130 (sep. pp. 1-50). 28. BORZA Al. 1941. Die Fortschritte der botanischen Forschung und des Naturschutzes in Rumänien. Nova Acta Leop., N. F., Halle (Saale) 10: 1-10 + 2 Tab. 29. BORZA Al. 1941. Die Fortschritte der botanischen Forschung und des Naturschutzes in Rumänien. Contribuţiuni Bot. Cluj-Timişoara 4(1): 1-12. 30. BORZA A. 1941. Die Pflanzenwelt Rumäniens und ihr Schutz. Ber. Deutsch. Bot. Ges. Berlin, 59(5): 153-168 + 1 charta. 31. BORZA A. 1943. Schedae ad “Floram Romaniae exsiccatam”. Cent. XXIV-XXV (No. 2301-2500). Bul. Gr d. Bot. Cluj, 1943, 23(1-2): 1-66. 32. BORZA A. 1944. Schedae ad “Floram Romaniae exsiccatam”. Cent. XXVI (No. 2501-2600 + Addenda). Bul. Gr d. Bot. Cluj, 1944, 24(1-2): 30-75. 33. BORZA A. 1947-1949. Conspectus Florae Romaniae Regionumque affinium. Cluj. (Pp. i-vii, 1-160 in 1947; pp. 161-360 in 1949). 34. BORZA Al. 2005. Protec iunea naturii: pagini alese (Nature protection: selected papers). Camerino 2005, L’uomo e l’ambiente - 45: 1-376 pp. Edi ie îngrijit de (Edited by) prof. dr. Vasile Cristea (ClujNapoca) şi (and) prof. dr. Franco pedrotti (Camerino). Camerino, Università degli Studi, 2005. 52 35. BORZA Al. 2005. Protec iunea naturei în România. Pp. 11-28. Reimpr.: BORZA Alexandru. Protec iunea naturii: pagini alese (Nature protection: selected papers). Camerino 2005, L’uomo e l’ambiente - 45: 1-376 pp. Edi ie îngrijit de (Edited by) prof. dr. Vasile Cristea (Cluj-Napoca) şi (and) prof. dr. Franco Pedrotti (Camerino). Camerino, Università degli Studi, 2005. 36. BORZA Al. 2005. Problema protec iunei naturii în România ● The problem of the protection of nature in Roumania. Pp. 52-93. Reimpr.: BORZA Alexandru. Protec iunea naturii: pagini alese (Nature protection: selected papers). Camerino 2005, L’uomo e l’ambiente - 45: 1-376 pp. Edi ie îngrijit de (Edited by) prof. dr. Vasile Cristea (Cluj-Napoca) şi (and) prof. dr. Franco pedrotti (Camerino). Camerino, Università degli Studi, 2005. 37. BORZA Al. 2005. Monumentele naturii în România. Pp. 94-112. Reimpr.: BORZA Alexandru. Protec iunea naturii: pagini alese (Nature protection: selected papers). Camerino 2005, L’uomo e l’ambiente - 45: 1-376 pp. Edi ie îngrijit de (Edited by) prof. dr. Vasile Cristea (Cluj-Napoca) şi (and) prof. dr. Franco pedrotti (Camerino). Camerino, Università degli Studi, 2005. 38. BORZA Alexandru. 2005. IX. Partie. Die Excursionrute durch die Dobrogea und das Donaudelta. Pp. 201-215. In: A. BORZA (red.), Guide de la sixième excursion Phytogeogra-phique internationale, Roumanie. Cluj: Miner-va, 243 pp. + 18 Pl. + 1 hart color. Reimpr.: BORZA Alexandru. Protec iunea naturii: pagini alese (Nature protection: slected papers). Camerino 2005, L’uomo e l’ambiente - 45: 1-376 pp. Edi ie îngrijit de (Edited by) prof. dr. Vasile Cristea (Cluj-Napoca) şi (and) prof. dr. Franco pedrotti (Camerino). Camerino, Univer-sità degli Studi, 2005. 39. C LINESCU Raul. 1937. Focele dela Capul Caliacra. Natura (Bucureşti), /Ser. II/, 26(9): 396-401. 40. C LINESCU R. I. 1934. Dobrogea şi Marea Neagr biomorfogenetice. Analele Dobrogei 15. ca individualit i geografice şi regiuni 41. C LINESCU R. I. 1935. Cutreerând Dobrogea meridional . Adev rul, 1935. 42. CIOCÂRLAN V. 1975. Agrostis moldavica Dobr. et Beldie dans la flore de R. P. Bulgarie et quelques considerations critiques sur ce taxon et d’autres taxa apparentes de l’espèces collective A. stolonifera L. Pp. 244-246. In: ANONIM, “Problems of Balkan Flora and Vegetation”, Sofija. 43. CONSTANTINEANU I. C. 1916. Über einige neue rumänische Uredineen. Ann. Mycol. 14(3/4): 248255. 44. CONSTANTINEANU I. C. 1920. Uredinée de Roumanie. Ann. Sci. Univ. Jassy 10(3-4): 314-460. 45. CRETZOIU Paul. 1934. Distribu ia geogra-fic a speciei Fraxinus Pallisae în Peninsula Balcanic ● La distribution géographique de Fraxinus Pallisae dans la Péninsule Balcanique ● Die geohraphische Verbreitung der Fraxinus Pallisae in der Balkanhalbinsel. Revista P dur. 46(12): 889-891. 46. CRETZOIU P. 1935. Not despre lichenii de la Capul Caliacra ● Notes from lichenes at Caliacra Cape. Revista Şti. “V. Adamachi” 21(2-3): 123. 47. CRETZOIU P. 1936. Lichenii de la Capul Caliacra ● lichenes from Caliacra Cape. Revista Şti. “V. Adamachi” 22(3-4): 163-164. 48. CRETZOIU P. 1936. Die Pallis’sche Eschen in Rumänien und auf des Balkanhalbinsel. Zeitschr. Für Weltforstwirt-schaft Bd. III, Heft 6/8 (1936). 49. CRETZOIU P. 1938. Rhododendron ponticum L. In: L. DIEL & G. SAMUELSSON, „Die Pflanzenareale“, 1 Karte und 1 p. text. 53 50. CRETZOIU P. & NEUWIRTH J. 1934. Zur Kenntnis der Flora des Bezirkes Caliacra in Dobrogea. Repert. Sp. Nov. 36: 311(327)-323(339). Süd- 51. CRETZOIU P. & NEUWIRTH Jan. 1935. Not asupra câtorva plante din p durile jude ului Durostor ● Note sur quelques plants des forêts de Durostor. Revista P dur. 47(7-8): 511-514. 52. DEMETRESCU C. A. 1915. Not de câteva plante recoltate din Bulgaria în timpul campaniei din vara anului 1913 ● Notes sur quelques plantes récoltes en Bulgarie en 1913. Bucureşti: Inst. Arte Grafice “Eminescu”, 1915, 16 pp. 53. DIMONIE M/ihail/. 1934. Valea Batovei ● Batova Valley. Natura (Bucureşti), /Ser. II/ 23(3): 29-32. 54. DIOSCORIDES. 1499. De Materia Medica. Venezia, Ed. I, mense Iulio, apud Aldum. In folio. 55. DIOSCORIDES, PEDANIOS. 1518. De medica materia libri sex. Marcello Virgilio tr. comm. Florentiae: Florentini. 56. DIOSCORIDES, PEDANIOS. 1906-1914. Πε τ ϋ η ατ , I-III (ed. Max Well-mann). Berlin. 57. DR GULESCU Constantin ● . 1987. Despre autenticita-tea denumirilor dacice de plante din lucr rile lui Dioscorides şi Pseudo-Apuleius ● Sur l’authenticité des dénominations daces des plantes des travaux de Dioscorides et de Pseudo-Apuleius ● On the authenticity of the Dacian names of plants from Dioscorides and Pseudo-Apuleius works ● . Revista Muzeelor Monum. - Muzee (Bucureşti) 24(7): 73-75. 58. DR GULESCU Constantin ● . 1988. Contribu ii la istoria botanicii populare româneşti ● Contribution à l’histoire de la botanique populaire roumaine ● Contribution to the history of the Romanian folk botany ● . Revista Muzeelor Monum. - Muzee (Bucureşti) 25(9): 80-84. 59. GEORGESCU Const. C. 1930. Atacul de l custe din p durile Dobrogei de Sud ● Eine neue Insektenkalamität in den Wäldern der Süddobrogea. Revista P dur. 42(7): 799-809. 4 fig./. 60. GEORGESCU C. C. & CIOBANU I. R. 1966. Contribu ii la cunoaşterea unor specii de Quercus din R. P. Bulgaria ● Contribution à la connaissance de quelques Quercus species de Bulgarie. Stud. Cercet. Biol., Ser. Bot. 18(1): 3-6. 61. IONESCU DOBROGEANU M. 1913. Din notele de c l torie ale lui Ewlia în a doua jum tate a veacului al XVII-lea. Bul. Soc. Regale Române de Geogr. 34(1): 210-223. /Recension from: Tariki-Scyah, Histoire du voyageur, ou voyages d’Evvlia. 4 vol./. 62. NEGREAN G. 1997. VELCHO I. VEL-CHEV, STEPHAN I. KOZHUHAROV, MINCHO E. ANCHEV (red.), Atlas na endemichnite rasteniya v Bulgariya (Atlas of the Endemic Plants in Bulgaria), Sofiya, 1992, 204 pp., 164 fig. color and charta. ISBN 954-430-004-X. Stud. Cercet. Biol., Ser. Biol. Veg. 49(1-2): 142-143. /recensionen/. 63. NEGREAN Gavril, CONSTANTINESCU Ovidiu & DENCHEV Cvetomir M. 2004. Addition to the Peronosporales of Bulgaria. Mycologia Balcanica 1(1): 69-72. 64. NEGREAN Gavril & DENCHEV Cvetomir M. 2000. New record of Bulgarian parasitic fungi. Flora Mediterranea (Palermo) 10: 101-108. 65. NEGREAN Gavril & DENCHEV Cvetomir M. 2002. New record of fungi from bulgarian Dobrudzha. Pp. 21-24. In: N. RANDJELOVIĆ (ed.), Proceedings of Sixth Symposium on Flora of Southeastern Serbia and Adjacent Territories, July 4-7, 2000, Sokobanja, Yugoslavia. Vuk Karadžić, Niš. 54 66. NEGREAN Gavril & DENCHEV Cvetomir M. 2004. Addition to the Erysiphales of Bulgaria. Mycologia Balcanica 1(1): 63-66. 67. NEGREAN G. & PETRESCU M. 2008. Uredinales species on Salix from Romania. S n tatea Plantelor (Bucureşti). (in press). 68. NEGREAN G. & PETRESCU M. 2001. Eudarluca caricis, ciuperc parazit pe uredinalele salicaceelor • Eudarluca caricis, a Fungus Parasiting the Uredinales of Salicaceae. Acta Horti Bot. bucurest. 29: 87-98. 69. NYÁRÁDY E. Gyula. 1942. Új növények a Délkeleti-Kárpátok és a Feketetenger vidékének flórájához - Plantae novae ad floram regionum Carpatorum meridionali-orientalium et Ponti Euxini. Acta Bot. (Szeged) 1(1-6): 31-45. 70. NYÁRÁDY E. I. 1928. Studiu preliminar asupra unor specii de Alyssum din Sec ia Odontarrhena. Vorstudium über einige Arten der Section Odontarrhena der Gattung Alyssum. Bul. Gr d. Bot. Cluj., 1927, 7(1-2): 3-51 + 10 Pl. 71. NYÁRÁDY E. I. 1928. Studiu preliminar asupra unor specii de Alyssum din Sec ia Odontarrhena. Vorstudium über einige Arten der Section Odontarrhena der Gattung Alyssum (Fortsetzung). Bul. Gr d. Bot. Cluj, 1927, 7(3-4): 65-160. 72. NYÁRÁDY E. I. 1929. Studiu preliminar asupra unor specii de Alyssum din Sec ia Odontarrhena. Vorstudium über einige Arten der Section Odontarrhena der Gattung Alyssum. Bul. Gr d. Bot. Cluj. (1929), 9(1-2): 1-68 /germ./. 73. PAN U Z. C. 1925(?). Capul Caliacra şi Litoralul nisipos de la Ecrene (Schi de vegeta ie). Anuarul liceului ortodox român «Andrei Şaguna» din Braşov (LX şi LXI). Anul jubiliar: 1924-1925, al 75-lea an şcolar, pp. 49-53. 74. PAN U Z. C. 1926. Contribu iuni la flora Dobrogei nou adic a jude elor Caliacra şi Durostor. Memor. Secţ. Şti., Academia Român , Ser. III, tom 3: 51-177. 75. PAN U Z. C. 1931. Geraniaceele din România. Studiu monografic ● /Geraniaceae from Romania. Monographic studies/. Memoriile Secţ. Şti., Academia Român , Ser. 3, T. 8, Mem. 1: 1-143 + 12 tab. 76. PAN U Z. C. & SOLACOLU T. 1925. O excursiune botanic în jude ul Caliacra ● /Botanical excursion in Caliacra district/. Publ. Soc. Naturaliştilor România 7: 11-23. 77. PAPP C. 1935?. Schi geobotanic asupra v ii Pârîului Bolota ● Esquise géobotanique sur la Vallée du ruisseau Bolota. Bul. Soc. Regal Român Geogr. 50: 1-21 (extrasul, pe care anul este 1936). 78. PAPP C. 1935. Despre vegeta ia briofil din p durile Sud-vestice Dobrogene. Bul. Gr d. Bot. Cluj 15: . 79. PAŞCOVSKI S. 1938. Contribu iuni la flora Cadrilaterului ● Beiträge zur Kenntnis der Flora der SüdDobrudschea. Revista P dur. 50(3): 241-248. 80. PAŞCOVSKI S. 1938. Contribu iuni la flora Cadrilaterului ● Beiträge zur Kenntnis der Flora der SüdDobrudschea. Inst., Cercet. Exper. Forest., ser. II, nr. 28. 81. PETRESCO C. 1915. Plantes nouvelles pour la flore de Dobrogea. Ann. Sci. Univ. Jassy 9(3-4): 357364. 82. PETRESCU C. 1915. Plantes nouvelles pour la flore de Dobrogea. Bull. Sect. Sci., Acad. Roumaine 4(3): 143-145. 55 83. PETRESCU C. 1915. Plantes nouvelles pour la flore de Dobrogea (Deuxième note). Bull. Sect. Sci., Acad. Roumaine 4(5): 216-220. 84. PETRESCO C. 1916. Plantes nouvelles pour la flore de Dobrogea (Deuxième note). Ann. Sci. Univ. Jassy 10(1): 90-94. 85. PETRESCU C. 1916. Plantes nouvelles pour la flore de Dobrogea (Troisième Note). Bull. Sect. Sci., Acad. Roumaine 4(7): 286-296. 86. PETRESCU C. 1916. Plantes nouvelles pour la flore de Dobrogea (Quatrième Note). Bull. Sect. Sci., Acad. Roumaine 4(8): 318-322. 87. PETRESCU Mircea & NEGREAN G. 1994. Uredinalele de pe speciile de Populus din România (I) ● Uredinales on Populus species from Romania (I). Stud. Cercet. Biol., Ser. Biol. Veg. 46(1): 13-21. 88. PETRESCU Mircea & NEGREAN G. 1995. Uredinalele de pe speciile de Populus din România (II) ● Uredinales on Populus species from Romania (II). Stud. Cercet. Biol., Ser. Biol. Veg. 47(1): 13-23. 89. POP E. 1926. Prin Dobrogea de Sud. I-IV. Renaşterea, Cluj 6(36-39) : .. 90. POP E. 1929. Bibliografia botanic a Dobrogei (1878-1928). Bul. Gr d. Bot. Cluj 9(3-4): 210-220. 91. POP E. 1931. Vitis sylvestris Gmel. în România ● Vitis sylvestris Gmel. en Roumanie. Bul. Gr d. Bot. Cluj 11(3-4): 78-93. 92. POP E. 1934. Equisetum maximum Lam. din România. Bul. Gr d. Bot. Cluj, 1933, 13(1-4): 78-85. 93. POP E. 1937. Equisetum maximum Lam. din România, II. Bul. Gr d. Bot. Cluj, 1936, 16(1-4): 1-17. 94. PRODAN I. 1925. Plante noi şi rare din Dobrogea Nou (Cadrilater) - Neue und seltene Pflanzen aus Neudobrogea (Südostrumänien). Bul. Gr d. Bot. Cluj 5(1-2): 38-41. 95. PRODAN I. 1923. Flora pentru determina-rea şi descrierea Plantelor ce cresc în Româ-nia. Cluj: Edit. Cartea Româneasc . Vol. I, II. 96. PRODAN I. 1923. Flora critic a Dobrogei. Analele Dobrogei 4: 219-248; 345-370. Separat Pp. I-56. Cluj: Victoria. 97. PRODAN I. 1923. Flora critic a Dobrogei. Constan a: Institutul de Arte Grafice »Victoria» George I. Georgescu, Pia a Indep., Palatul Prim riei, p. 1-56. 98. PRODAN I. 1924. Scurt fitogeografie a Dobrogei. (Esquisse d’une phytogéographie de la Dobrogea). Lucr. Inst. Geogr. Univ. Cluj - Trav. Inst. Géogr. Univ. Cluj (Roumanie), 1922. 1. 311-319; 345-370. Separat Pp. 1-56. Cluj: Victoria. 99. PRODAN I. 1925. Plante noi şi rare din Dobrogea Nou (Cadrilater) - Neue und seltene Pflanzen aus Neudobrogea (Südostrumänien). Bul. Gr d. Bot. Cluj 5(1-2): 38-41. 100. PRODAN I. 1926. Plante noi şi rare din Dobrogea nou . Bul. Gr d. Bot. Cluj 5: 38-41. 101. PRODAN I. 1927. Centaureele din România (Centaureae Romaniae). Studiu monografic cu numeroase planşe în text şi cu tabele. Publ. Soc. Natur. România 9: 105-164. 102. PRODAN I. 1928. Flora mic ilustrat a României. Cluj: Edit. Minerva, 518 pp. 103. PRODAN I. 1928. Eine neue Euphorbia-Art aus Dobrogea. Cluj: Edit. Minerva, 2 pp. 104. PRODAN I. 1928. Eine neue Onosma-Art aus Dobrogea, O. pontica. Cluj: Edit. Minerva, 2 pp. 105. PRODAN I. 1928. Neue Pflanzen aus der Dobrudscha. Cluj: Edit. Minerva, 4 pp. 56 106. PRODAN I. 1930. Centaureele României (Centaureae Romaniae). Monographie. Cluj: Inst. Arte Grafice "Ardealul", 256 pp. + 43 tab. + 63 Pl. + 3 h r i. 107. PRODAN I. 1930. Plantae novae et rarae. Bul. Acad. Înalte Stud. Agron. Cluj No. 1: 38-57. + 2 Pl. 108. PRODAN I. 1930. Plantae novae et rarae. Cluj: Cartea Româneasc , 29 pp. + 2 Pl. /extras din Bul. Acad. Înalte Stud. Agron. Cluj No. 1: 38-57/. 109. PRODAN I. 1930. Descrierea speciilor, variet ilor şi formelor de Jurinea publicate din cuprinsul rii ● Beschreibung der aus unseren Vaterlande publizierte Arten, Varietäten und formen der Gattung Jurinea. Bul. Acad. Înalte Stud. Agron. Cluj No. 1: 63-76. 110. PRODAN I. 1930. Plantae novae et criticae. Pp. 379-394. In A. Borza & E. Pop, Întâiul Congres al Naturaliştilor din România -Premier Congrès National des Naturalistes de Roumanie - inut la Cluj dela 18 pân la 21 aprilie 1928. Tenu à Cluj du 18 au 21 Avril 1928. Cluj: Edit. Cartea Româneasc . 111. PRODAN I. 1931. Achilleele României - Achilleae Romaniae et descriptio aliquot specierum e Peninsula Balcanica nostris speciebus propinquarum facta. Monographie. Bul. Acad. Înalte Stud. Agron. Cluj. Memorii - Mémoires 2: i-iv + 1-68 + xliii tab. Cluj: "Cartea Româneasc ". 112. PRODAN I. 1931. Descrierea speciei Stachys leucoglossa Griseb. şi subspeciei caliacrae Prod.: 518520. Beschreibung von Stachys leucoglossa Griseb. und deren subspeciese caliacrae Prod. Bul. Acad. Înalte Stud. Agron. Cluj 2(1): 518-520. 113. PRODAN I. 1931. Deschreibung von Stachys leucoglossa Griseb. und deren Subspecies. Bul. Acad. Înalte Stud. Agron. Cluj 2(1): 520-523. 114. PRODAN Julius. 1931. Die Flora der Dobrudscha und einer kurzer Überlick über die Flora der Meeresküste Rumäniens. Bul. Minist. Agric. Domen. 6(11-12): 1-95. 115. PRODAN I. 1932. Trandafirii spontani şi cultiva i cunoscu i pân în prezent în România ● Die bisher Bekannten wildwachsende und angebauten Rosen Rumäniens. Bul. Acad. Înalte Stud Agr. Cluj 3: 333-477 + 59 Pl. 116. PRODAN I. 1932. Trandafirii spontani şi cultivaţi cunoscuţi pân în prezent în România ● Die bisher Bekannten wildwachsende und angebauten Rosen Rumäniens. Cluj: Tip. Na ional : 1-146 + 59 Pl. 117. PRODAN I. 1934. Conspectul Florei Dobrogei /partea I-a/. Bul. Acad. Înalte Stud. Agron. Cluj. 5(1): 175-342. 1934 /p. I/. 118. PRODAN I. 1935. Conspectul Florei Dobrogei /partea I-a/. (separat ex Bul. Acad. Înalte Stud. Agron. Cluj, 1934, 5(1). Pp. 1-170. Cluj: Tipografia Na ional S.A. 119. PRODAN I. 1936. Conspectul Florei Dobrogei. Bul. Acad. Înalte Stud. Agron. Cluj. 6: 204-261 + xlvi pl. /p. II/. 120. PRODAN I. 1936. Conspectul Florei Dobrogei. Partea II-a. Extras din Bul. Acad. Înalte Stud. Agron. Cluj. 6: 204-261 + xlvi pl. Cluj: Tipografia Na ional S. A. 1-57 + Pl. i-xlvi. 121. PRODAN I. 1935-1938. Conspectul Florei Dobrogei. Bul. Acad. Înalte Stud. Agron. Cluj. 5(1): 175342. 1935 /p. I/; 6: 204-261 + xlvi pl., 1936, /p. II/; 7: 16-102, 1938, (p.III). Et sep. 1-170, 1-57 + 46 pl., 196. 122. PRODAN I. 1935. Die Iris-Arten Rumäniens. Bul. Gr d. Bot. Cluj, 1934, 14(3-4): 105-198. 123. PRODAN I. 1936. Die Iris-Arten Rumäniens (Forsetzung). Bul. Gr d. Bot. Cluj, 1935, 15(1-4): 65-130. 124. PRODAN I. 1935. Die Iris-Arten Rumäniens. Cluj: Tipografia Na ional : 105-264 + 46 Pl. 57 125. PRODAN I. 1936. Conspectul Florei Dobrogei - partea II-a ● Le conspect de la flore de Dobrogea (en roumaine). Bul. Acad. Înalte Stud. Agron. Cluj, 1935-1936, 6: 206-259 + 45 pl. 126. PRODAN I. 1936. Conspectul Florei Dobrogei - partea II-a. (separat din Bul. Acad. Înalte Stud. Agron. Cluj, 1935-1936, 6). Cluj: Tipografia Na ional S.A. Pp. 1-60 + 46 pl. 127. PRODAN I. 1938. Conspectul Florei Dobrogei - partea III-a. Bul. Acad. Înalte Stud. Agron. Cluj. 7: 16102. 128. PRODAN I. 1939. Conspectul Florei Dobrogei - partea III-a. (Separat din Bul. Acad. Înalte Stud. Agron. Cluj. 1938, 7: 1-96 (incl. 30 pl.). Cluj: Tipografia Na ional S. A. 129. PRODAN I. 1938. Conspectul Florei Dobrogei. Bul. Acad. Înalte Stud. Agron. Cluj. (sep.): 1-170, 1-57 + 46 pl., 1-96. 130. PRODAN I. 1938. Flora Dobrogei Nou (Cadrilaterul). Bul. Fac. Cern uţi 11: 271-320. 131. PRODAN I. 1938. Flora Dobrogei Nou (Cadrilaterul). Analele Dobrogei 19(1): 120-169. 132. PRODAN I. 1939. Considera iuni critice asupra unor specii din genul Iris. (Kritische Betrachtungen über einige Iris-Arten). Anal. Acad. Înalte Stud. Agron. Cluj.(1939/40), 8: 367-406. 133. PRODAN I. 1939. Flora pentru determinarea şi descrierea plantelor ce cresc în România. Ed. II. Cluj: "Cartea Româneasc ". 1 (p. 1), (i-cix + 1-624 pp.); 1 (p. 2) (625-1278 pp.). 2 (1-713 pp.) + Addenda (1 & 2): 1-31. 134. PRODAN I. 1939. Flora mic ilustrat a României. Ed. II-a. Cluj: Inst. Arte Grafice “Ardealul”, 560 pp. 135. PRODAN I. 1951. Specii de Potentilla aflate şi studiate în herbarul Universit ii din Cluj ● /Potentilla species from Cluj University Herbarium/. Analele Acad. Române, Ser. Geol., Geogr., Biol., Şti. Tehn. Agric., 1950, Tom ii, Mem. 17: 643-660. 136. PRODAN I. 1951. Specii din genul Centaurea aflate şi studiate în Herbarul Universit ii din Cluj ● Centaurea species from Cluj University Herbarium/. Analele Acad. Române, Ser. Geol., Geogr., Biol., Şti. Tehn. & Agric., Tom. III, Memoriul 18: 661-694. 137. PRODAN I. 1957. Contribu ii la flora R.P.R. şi a rilor învecinate: U.R.S.S., R.P.F. Iugoslavia, R.P. Bulgaria, R.P. Ungar ● Contributions à la Flore de la République Populaire Roumaine et des pays voisins [U.R.S.S., Yougoslavie, République Populaire Bulgare et République Populaire Hongroise] ● ч . Н. . coce , CCCP, c H. . ., Н. ., Н. . Stud. Cercet. Biol., Acad. Român , Filiala Cluj, 8(1-2): 69-93. 138. PÉNZES A. 1948. Néhány új növényalak Bulgáriából ● Some new plant forms from Bulgaria. Borbásia 8(1-8): 3-9. 139. S VULESCU T. 1928. Herbarium Mycolo-gicum Romanicum. Fasc. 1-2 (nr. 1-100). Bucureşti, 1 IX 1928. 140. S VULESCU T. 1930. Herbarium Mycolo-gicum Romanicum. Fasc. 3-4 (nr. 101-200). Bucureşti. 141. S VULESCU T. 1931. Herbarium Mycolo-gicum Romanicum. Fasc. 5-6 (nr. 201-300). Bucureşti. 142. S VULESCU T. 1932. Herbarium Mycolo-gicum Romanicum. Fasc. 7-10 (nr. 301-500). Bucureşti. 143. S VULESCU T. 1934. Herbarium Mycolo-gicum Romanicum. Fasc. 11-14 (nr. 501-700). Bucureşti. 58 144. S VULESCU T. 1935. Contribution à la connaissance des Ustilaginées de Roumanie. Analele Inst. Cercet. Agron. România., anul 6, 7: 347-430 + 35 Pl. (1-86 + xxxv). 145. S VULESCU T. 1936. Contributions à la connaissance des Ustilaginées de Roumanie. Analele Inst. Cercet. Agron. României, 1935, anul 6, vol. 7: 1-86 + XXXV. & separat: Bucureşti: Imprimeria Na ional , 86 pp. + 35 Pl. 146. S VULESCU T. 1938. Contribution à la connaissance des macromycetes de Roumanie. Mem. Sect. Şti., Acad. Român , Ser. iii, T. XIII, Mem. 8: 267-338 + 5 Pl. 147. S VULESCU T. 1938. Nouvelle contribu-tion à la connaissance des Péronosporacées et Ustilaginacées de Roumanie. Bull. Sect. Sci. Acad. Roumaine 20(7): 1-7. 148. S VULESCU T. 1939. Contribution à la connaissance des Urédinées de Roumanie. Bull. Sect. Sci. Acad. Roumaine 21(3-4): 41-51. 149. S VULESCU T. 1939. Contribution nouvelle à la connaissance des Urédinées de Roumanie. Bull. Sect. Sci. Acad. Roumaine 22(2): 86-103. 150. S VULESCU T. 1939. Herbarium Mycolo-gicum Romanicum. Fasc. 15-24 (nr. 701-1200). Bucureşti. 151. S VULESCU T. 1940. Herbarium Mycolo-gicum Romanicum. Fasc. 25 (nr. 1201-1250). Bucureşti. 152. S VULESCU T. 1944. Matériaux pour la flore des Uredinées de Roumanie. Supplément. Bull. Sect. Sci. Acad. Roumaine 26(5): 308-332. 153. S VULESCU T., cura: BONTEA Vera & CONSTANTINESCU O. 1968. Herbarium Mycologicum Romanicum “Tr. S vulescu”. Schedae. Fasc. I-XIX (nr. 1-950). Bucureşti. pp.: i-iv + 1-481. 154. S VULESCU T., cura: BONTEA Vera & CONSTANTINESCU O. 1968. Herbarium My-cologicum Romanicum “Tr. S vulescu”. Schedae. Fasc. XX-XXXV (nr. 951-1750). Bucureşti. pp.: i-ii + 482-957. 155. S VULESCU T. & RAYSS T. 1930. Con-tribution à la connaissance des Péronosporacées de Roumanie. Ann. Mycol. 28(3-4): 297-320. 156. S VULESCU Tr. & RAYSS T. 1932. Nouvelle contribution à la connaissance des Péronosporacées de Roumanie. Ann. Mycol. 30(3-4): 354-385. 157. S VULESCU Tr. & RAYSS T. 1935. Quatrième contribution à la connaissance des Péronosporacées de Roumanie. Ann. Mycol. 33(1-2): 1-21. 158. S VULESCU T. & SANDU-VILLE C. 1933. Beiträg zur Kenntnis der Micromyceten Rumäniens. Hedwigia 73(3-4): 71-132. 159. S VULESCU T. & SANDU-VILLE C. 1935. Beitrag zur Kenntnis der Micromyceten Rumäniens. Hedwigia 75(3-4): 159-233. 160. S VULESCU T. & SANDU-VILLE C. 1940. Quatrième contribution à la connaissance des micromycètes de Roumanie. Mem. Secţ. şti., Acad. Român , Ser. III, T. XV, 1939-1940, Mem. 17: 397(1)502(106) + 15 Pl. 161. S VULESCU T. & S VULESCU Olga. 1937. Beitrag zur Kenntnis der Uredineen Rumäniens. Ann. Mycol. 35(2): 113-118. 162. S VULESCU T. & S VULESCU Olga. 1937. Uredineae novae Romaniae. Pp. 213-218 + 1 pl. In: ANONIM, “Hommage au Professeur E. C. Teodoresco”. Bucureşti. 59 163. S VULESCU T. & S VULESCU Olga. 1941. Matériaux pour la flore des Urédinées de Roumanie. Analele Acad. Române, Mem. Secţ. şti., Ser. III, Tom. 17, Mem. 4: 113(1)-261(148). 164. ŞERB NESCU Maria. 1939. Contribu iuni la studiul florei V ii Batovei ● Floristic contribution to the Batova Valley. Bul. Soc. Studenţilor Natur., 1939, 8, 9, 10: 1-4. 165. STOICULESCU Cristian D. 1964. P durea columnei vorbeşte ● The Column’s forest work. Almanahul P durii 1965, pp. 11-14. 166. STOICULESCU Cr. D. 1985. Traian’s Column documentary value from a forestry viewpoint, part. I, Dacia, ser. nou , nr. 1-2, ian.-dec., pp. 81-98. 167. STOICULESCU Cristian D. 1987. Valoa-rea documentar a Columnei traiane pentru silvicultur (partea I-a) ● Trajan’s column documentary value for forestry (part one). Pp. 39-68. In: Ştefan PASCU, Emil NEGRU IU, Victor GIURGIU & Nicolae BOŞCAIU (sub red.). “P durea şi poporul român”, Cluj-Napoca, 1987. 60 MACROPHYTOBENTHOS EVOLUTION UNDER PRESENT ENVIRONMENTAL QUALITY OF ROMANIAN BLACK SEA COASTAL WATERS AS TO EARLIER DECADES Daciana SAVA*, Alexandru S. BOLOGA** * Universitatea Ovidius Constanţa, Facultatea de Ştiinţe ale Naturii şi Ştiinţe Agricole B-dul Mamaia, nr. 124, Constanţa, 900527, România, dacianas@yahoo.com ** National Institute for Marine Research & Development “Grigore Antipa”, Mamaia 300, RO-900581, Constanta 3, Romania, e-mail: abologa@alpha.rmri.ro __________________________________________________________________________________________ Abstract: More than a century has passed since macroalgal flora was studied for the first time by Russian and Romanian scientists, and later on by Bulgarian, Turkish and Georgian ones. Several decades ago these studies showed a much higher number of taxa as presently found in the coastal waters. This paper shows the latest data on macrophytic algae from the Romanian littoral, after a five years long survey along the coast, in seven sites situated between Constan a and 2 Mai, in different periods of the year compared with previous data, in order to point out the gradual decline of this major component of the Black Sea ecosystem, with special emphasize on endangered taxa. The algae were collected from various types of hard substratum, and from each sample, algae were identified and representative individuals were kept and dried for the herbarium collection. For biomass estimation three samples were randomly taken from a surface of 100 cm2 at each depth (between 0,5 - 7 m), and the algal material was dried 24 hours at 1050C and weighed. The present observations show that the Romanian Black Sea coastal zone has been subjected to severe ecological disturbance during the last five decades; and as a result of complex and multiple anthropogenic pressures and with unfavourable natural factors, a considerable reduction of macroalgal species is evident within the general decline of biodiversity. Keywords: macrophytobenthos, Romanian Black Sea coast, Chlorophyta, Phaeophyta, Rhodophyta __________________________________________________________________________________________ Introduction More than a century has passed since macroalgal flora was studied for the first time by Russian and Romanian scientists, and later on by Bulgarian, Turkish and Georgian ones. The beginning of marine benthal algology at the Romanian Black Sea coast is marked out by the first information about native algal flora found in A. Kanitz (1881), where J. Schaarschmidt listed 233 species of algae, out of which 50 marine, and only six macrophyta are mentioned. In 1907, E. Teodorescu published a monograph of the algological flora from Romania (both fresh and marine waters) were 32 species of macrophyta where mentioned in samples taken from rocky bottoms along the Romanian coast (Teodorescu, 1906). The most decisive step in the development of marine biology in general and algology in particular, is the foundation of the Marine Zoological Station at Agigea in 1926 by I. Borcea, and of the Bio-oceanographic Institute in Constanta in 1932 by G. Antipa. Starting her activity in 1930, the outstanding algologist Maria Celan contributed with taxonomical, cytological and ecological research upon macrophytic vegetation from the Black Sea coast. Celan’ s contribution was represented by: first distinction made between the two species of Cystoseira (Celan, 1935), new macroalgal species described for the Black Sea or for the Romanian sector (Celan, 1936; Celan, 1938), cytological studies (Celan, 1940), taxonomical studies (Celan, 1948; Celan, 1958; Celan et Serb nescu, 1959Celan, 1960; Celan, 1977). Later, together with A. Bavaru, the studies were extended to algal communities (Celan et Bavaru, 1973; Celan et Bavaru, 1978). 61 Important contributions to the knowledge of algal flora belong to H. V. Skolka, who was the first to describe the repartition of red algae Phyllophora (Skolka, 1956), and continued the observations regarding macroalgae phytocoenoses and their repartition along the shore (Skolka et Bodeanu, 1971; Skolka et al., 1980). Mainly after 1970, A. Bavaru completed his research in algal systematics and phytocoenology, with contributions on the macrobenthic vegetation in general (Bavaru, 1970; Bavaru, 1977; Bavaru, 1981) and especially Cystoseira populations (Bavaru, 1971; Bavaru, 1972). Research on macroalgae extended also to their physiology and chemistry; e.g., A. S. Bologa studied the photosynthetic productivity of benthic algae (Bologa, 1979; Bologa, 1980), as well as their capacity to accumulate radioactive isotopes, representing useful bioindicators for this type of pollution (Bologa et al., 1983). Several decades ago these studies showed a much higher number of species, subspecies and varieties as presently found in the coastal waters. The continuous quantitative and qualitative lowering of algal diversity and biomass becomes evident when analyzing the related literature. According to A.D. Zinova, in 1967, the Black Sea macroalgoflora totalized a number of 277 species with 74 Chlorophyta, 3 Xanthophyta, 71 Phaeophyta and 129 Rhodophyta (Zinova, 1967). But research carried out after 1970 showed a gradual impoverishment, especially from the qualitative point of view, of the macroalgal flora. The observations on the both qualitatively and quantitatively decline of macroalgal flora, initiated by Celan, were confirmed. In 1969, only 77 species were identified (Skolka, 1969), later, in 1977, 86 species (Bavaru, 1977), and 69 and 55 respectively, after 1980 (Vasiliu, 1984; Vasiliu, 1996). It is considered that these changes are due to a number of causes such as: massive frosts, silting of the rocky bottom with suspended matter, decrease of light penetration in the water column due to same suspensions, increase of eutrophication (Bologa, 1987-1988). So, it is evident that increasing eutrophication and pollution have considerably changed the structure and functioning of the Black Sea ecosystem, mainly in its NW corner, where human activities, discharge of polluted fresh waters, inflow of sewage and industrial wastes, affected both the qualitative and quantitative state of benthic and planktonic communities; that is why macrophytobentos has shown a gradual and continuous decline. In the last 20 to 30 years, the phytal zone on the NW shelf has shrunk to a tiny fraction of its previous size: at present, the area where macrophytobenthos can develop is only a narrow inshore strip, between 2 to 7 m depth which is the only zone where there is enough light for photosynthesis. Knowing the importance of algae as food and shelter for animals as well as source of oxygen and external metabolites, such a decline is catastrophic for benthic life and for the entire ecosystem of in this part of the Black Sea. Unfortunately very few research has been carried out today regarding the present state of the macroalgal flora (Bologa, 2001). Taking this in consideration, a new approach of such studies is absolutely necessary in order to establish the major modifications that occurred in the state of macrophytobenthos, under the influence of harmful factors that disturbed the quality of marine environment and biodiversity (Bologa et Sava, 2006; Sava, 2002). The paper shows the latest data on macrophytic algae along the Romanian littoral, after a five years long survey along the coast, compared with previous data, in order to point out the gradual decline of this major component of the Black Sea ecosystem, with special emphasize on endangered taxa. Material and Methods Sampling stations One of the most important conditions for the development of macrophytes is the presence of a hard substratum, of various types. Therefore, the selection of study sites considered as principal criteria the presence of a rocky, natural or artificial bottom, In some cases, the algae were collected from the shells of mussels that covered the whole surface of rocky bottoms. The location of the sampling station covered a length of over 60 km, between Constanta to 2 Mai, close to Bulgarian border. The locations of the study sites as well as the sampling depths are illustrated in Table 1 and Figure 1. 62 Table 1 - Sampling stations of macrophytobenthos, with indication of transects and depths No. Sampling station 1. Constanta 2. 3. Agigea Eforie Nord 4. 5. 6. Eforie Sud Costinesti Mangalia 7. 2 Mai Transect Bottom type Cazino Trei Papuci Pescarie Rocky -natural Rocky- natural rocky / tetrapods natural and artificial rocky -natural rocky / tetrapods – natural and artificial dam rocky- natural rocky / tetrapods –natural and artificial Rocky –natural Sampling depth 0.5 to 1 m 0.5 to 1 m 0.5 to 4 m 0.5 to 1 m 0.5 to 1 m 0.5 to 3 m 0.5 to 3 m 0.5 to 6 m 0.5 to 5 m Fig.1 - The location of sample stations along the Romanian Black Sea coast The research has been carried out between 2000 and 2005, in different periods of the year, both in warm and in cold season, in order to collect macroalgal species that develop all year round together with the species that could only be found in certain periods of the year. Qualitative determinations Samples for qualitative determinations have been collected from various depths between 0.5 and 6 m, in plastic bags, together with a label, mentioning place and time of collection. All samples were brought fresh in the laboratory, carefully washed for sediments and associated fauna, and sorted out in three main groups: Chlorophyta (green algae), Phaeophyta (brown algae), Rhodophyta (red algae). Species identification was made macroscopically where possible, but for difficult genera, microscopic examination was necessary. Representative individuals were kept for herbarium collection. Quantitative measurements For accurate results regarding the major modification of the macrophytobenthos, quantitative determinations are also necessary giving the possibility to appreciate biomass dynamics of these algae during the last years, comparative with previous decades. The method used for quantitative measurements is a classical one, and in order to be adequate, certain requirements were respected, taking in consideration that sometimes sampling can be difficult, because of the irregular and diverse type of substratum, but, on the other hand, that algal samples must be representative for the studied algal population. In present work, the method of squares was used, using a metallic frame that covered a surface of 100 cm2. Three samples were collected from each station, transect and depth and each one was introduced in plastic bags and labeled. Samples were brought fresh into the laboratory, washed for the associated fauna and sediments, and dried in oven at 1050 C. The estimation of biomass was calculated from the mean weight of the three samples and appreciated as dry weight. Results and Discussions Qualitative results In the samples collected during six years of study, 16 Chlorophyta, 5 Phaeophyta and 10 Rhodophyta were found, as shown in the following list. CHLOROPHYTA Ord. ULVALES Fam. Ulotrichaceae 1. Ulothrix implexa (Kutz.) Kutz. 2. Ulothrix flacca (syn. U. pseudoflacca Wille) Dillw.Thur. 1. 2. 3. 4. 5. 6. Fam. Ulvaceae Ulva rigida Ag. (Fig.2) Enteromorpha intestinalis (L.) Link. Enteromorpha flexuosa (Wulf. et Roth) J.Ag. Enteromorpha compressa (L.) Grev. (Fig.3) Enteromorpha linza (L.) J.Ag. Enteromorpha prolifera (O.F.Mull) J.Ag. 1. 2. 3. 4. 5. 6. Ord. CLADOPHORALES Fam. Cladophoraceae Cladophora vagabunda (L.) Hoeck Cladophora albida (Huds.) Kutz. Cladophora sericea (Huds.) Kutz. Cladophora laetevirens (Dillw.) Kutz. Cladophora dalmatica Kutz. Chaetomorpha aerea (Dillw.) Kutz. Fam. Acrosiphonaceae 1. Urospora penicilliformis (Roth.) Aresh. Ord. BRYOPSIDALES Fam. Bryopsidaceae 1. Bryopsis plumosa (Huds.) Ag. 64 PHAEOPHYTA Ord. ECTOCARPALES Fam. Ectocarpaceae 1. Ectocarpus siliculosus (Dillw) Lyngb. 2. Ectocarpus confervoides (Roth) Le Jolis. Ord. SCYTOSIPHONALES Fam. Scytosiphonaceae 1. Scytosiphon lomentaria (Lyngb) J.Ag. Ord. PUNCTARIALES Fam. Punctariaceae 1. Punctaria latifolia Grev. Ord. FUCALES Fam. Cystoseiraceae 1. Cystoseira barbata (Good. et Wood.) Ag. RHODOPHYTA Ord. BANGIALES Fam. Bangiaceae 1. Porphyra leucosticta Thur. 2. Bangia fuscopurpurea (Dillw.) Lyngb. Ord. CRYPTONEMIALES Fam. Corallinaceae 1. Corallina officinalis L. Ord. RHODIMENIALES Fam. Champiaceae 1.Lomentaria clavellosa (Thurn.) Gail. (Fig.4) Ord. CERAMIALES Fam. Ceramiaceae 1. Ceramium rubrum (Huds.) C. Ag. (Fig.5) 2. Ceramium elegans (Roth.) Ducl. 3. Ceramium diaphanum (Lightf.) Roth. 4. Callithamnion corymbosum (Ducl.) Ag. Fam. Rhodomelaceae 1. Polysiphonia elongata (Huds.) Harv. 1. Ord. GIGARTINALES Fam. Phyllophoraceae Phyllophora pseudoceranoides (Gmel.) Newr.et A.Tayl. ( syn. P. membranifolia (Good. et Wood. ) J.Ag 65 Fig. 2 - Ulva rigida Ag. Fig. 4 - Lomentaria clavellosa (Thurn.) Gail. Fig. 3 - Enteromorpha compressa (L.) Grev. Fig. 5 - Ceramium rubrum (Huds.) C. Ag. Compared with previously reported results, it is very evident that the number of species from each phylum decreased over the years (Table 2). Analyzing both the present list and the table, several observations result: -about the exact number of species of macrophytes, opinions differ from author to author, as a result of incertitudes created by some forms and varieties and by the consideration of microscopic forms; -it is very obvious that, over the years, most species belonged to green algae. This can be explained by the fact that eutrophication, that generally has a negative influence on marine biota, favourized the development of green algae. Some genera like: Ulva, Enteromorpha, Cladophora persisted and proliferated under these environmental conditions; -as to the brown algae, the number of species also decreased and nowadays, only four cold season species were found; -red algae are also sensitive to pollution and their number has also decreased over the years, but some genera of red algae (Ceramium) can also develop in eutrophic waters, sometimes covering the hard substratum up to 90%; -another obvious fact is the lack of perennial species: only one such species was found in the samples (red alga Polysiphonia); Cystoseira barbata (brown) and Phyllophora (red) have been found in various locations along the shore during field trips, on the beach, teared out from their rocky bottom probably during storms; -the positive sign that can be pointed out is the reappearance of species that were considered lost for many years, such as Lomentaria clavellosa, but unfortunately, no exact data about its location and biomass could be achieved, as the thalli were collected from the beach, teared away from the rocky bottom. 66 Table 2 - Number of macroalgal species along the Romanian Black Sea coast identified between 1977 and 2002 Phyllum Bavaru, 1977 Vasiliu, 1980-1995 Sava,1995-2002 Chlorophyta 31 22 16 Phaeophyta 14 9 4 Rhodophyta 41 24 10 Total 86 55 30 It is evident that the benthic algal flora has endured a gradual, but continuous decline and the accentuation of this decline is not only due to natural factors but mainly to anthropogenic ones. Also, another important feature is the uniform aspect of the present vegetation and the fact that the new algal communities consist of a very small number of species. Nevertheless some of them, evinced considerable biomass. Quantitative results The qualitative data are completed with quantitative ones, allowing a better understanding of the structure and functioning of the algal populations. As it became evident from analyzing the samples, green and red algae were dominant, brown algae being represented by a few number of species, as a consequence, the biomass estimates were made only for the two major groups: Chlorophyta and Rhodophyta. The evolution of biomass since 200 evinced that green algae were dominant. Also for a complete image of the present state of macroalgal vegetation, the values of total biomass of both green and red algae, in all sampling sites are indicated (Table 3). Table 3. Total biomass of Chlorophyta (green algae) and Rhodophyta (red algae) between 2000 and 2005 (g/m3) Year Green algae Red algae 2000 2001 2002 2003 2004 2005 TOTAL 19,734 18,828 22,310 25,000 23,410 15,581 124, 863 17,845 17,910 20,802 18,010 21,772 7,830 104,169 It is once more evident that the green algae prevailed and the quantities of red algae are lower. The maximum development of green algae took place in 2003 (25,000 g/m2), but close values were registered also in 2002 (22,310 g/m2 ) and 2004 (23,410 g/m2). In 2005, a significant decrease of Chlorophyta biomass is evident, the total value being almost half (15,581 g/m2) of the one calculated for 2003. As to the red algae, the maximum value of biomass (21,722 g/m2) occurred in 2004, with slight differences compared with previous years, whereas in 2005 a reduced biomass was significant, with more than half values registered compared with the ones observed in 2000. 67 Even though the maximum values of green and red algae were not registered simultaneously, for 2005 it is evident that both decreased; this could be related to the amelioration of the state of the marine ecosystem along the Romanian shore in recent years, that could have beneficial consequences on the whole algal vegetation. It has to be point out that the high biomass of green algae is due to species belonging to the genera Ulva, Enteromorpha and Cladophora that develop all year round, together with Ulothrix and Urospora that develop only during the cold season (spring and autumn). But high biomasses of red algae are almost entirely owed to species of Ceramium, found on rocky bottom the entire year. During spring Porphyra, and sometimes Polysiphonia and Callithamnion contributed quantitatively. Only in the warm season these last two mentioned species were found in appreciable quantities in samples. This can be explained because Ceramium species, have a high capacity of both asexuate and sexuate reproduction, so they can easily and quickly populate the rocky bottoms, sometimes even completely. Conclusions As to the severe environmental degradation of the Black Sea ecosystem in general and of its NW sector in special, macrophytobenthos deserve a notable attention, as a key component of coastal waters. The impoverishment of the vegetation, starting in the ’50’s but very evident especially since 1970, is due to known natural and anthropic causes which deteriorated the quality of the marine environment (massive frosts registered in some years, progressive degradation of the marine coastal environment due to erosion, impurification of seawater quality due to increasing eutrophication, extension of hypoxia and even anoxia. These changes affected not only the macrophytobenthos, but all biological components of the ecosystem, e.g. the structure and the functioning of benthic and pelagic communities, as well the qualitative and quantitative state of all phyto and zoocommunities. Anthropogenic disturbances are still present, changing, directly and indirectly the ecosystem and community structure, by replacement of some phytocoenoses by others. Recent observations confirmed: qualitative decline (few number of species), the almost disappearance of perennial species (brown and red algae) this fact having as consequence disappearance of associated or epiphytic species, the uniformity of algal belts, that consist mainly of opportunistic species with a short life cycle, much lower productions compared with those of Cystoseira in previous years; non-stable equilibrium of macrophytic communities. The Romanian Black Sea coastal zone has been subjected to severe ecological disturbance during the last five decades; as a result of complex and multiple anthropogenic pressures together with unfavourable natural factors, a considerable reduction of macroalgal species within the general decline of biodiversity took place. Future needs for improving the existing situation may consider: • continuous biodiversity monitoring in order to enable observations of all changes that might occur; • continuous observation of the evolution of physical-chemical parametres of shallow waters, with valuable informations upon the environment quality but also upon the expected amelioration of the state of the marine ecosystem; • submission of projects that have to propose rapid but realistic rehabilitation programmes; • the maintenance of the Marine Reserve 2 Mai –Vama Veche in the south part of the Romanian Black Sea coast, and its extension across the Bulgarian border, in order to extend the interest in conserving biodiversity in both countries, and increasing the possibility of more sound related projects and reconstruction plans. References 1. 2. BAVARU A., 1970 – Consideratii generale asupra gruparilor vegetale algale din partea de N-V a Marii Negre. Com. Hidrobiol. SSA, 27-35 BAVARU A., 1977 – Contributii la studiul asociatiilor algale din faciesul de piatra de la litoralul romanesc al Marii Negre, Teza de doctorat, Universitatea Bucuresti, 195 pp 68 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. 20. 21. 22. 23. 24. BAVARU A., 1981 – Consideratii privind situatia actuala a vegetatiei algale macrofite de la litoralul romanesc al Marii Negre. Lucr. st. Inst. sup. Constanta, Biol., 97-101 BAVARU A., 1971 – Contributii la cunosterea Cystoseirelor de pe litoralul romanesc al Marii Negre – Com. Hidrobiol: 27-35 BAVARU A., 1972 – Evaluari cantitative in populatiile de Cystoseira la tarmul romanesc al Marii Negre- St. Cercet. Biol. Ser. Bot. 24, 2: 95-101 BOLOGA A. S., 1979 – Experiments on the photosynthetic rate in the alga Cladophora vagabunda L. under modified salinity and ionic rations – Rev Rom. Biol., Biol .veget., 24, 2:127-131 BOLOGA A. S., 1980 – Productivitatea fotosintetica a unor alge bentale marine – Teza de doctorat, Universitatea Bucuresti, 174 pp BOLOGA A. S., BALABAN D.P., CHIOSIL I., 1983 – Preliminary experimental data on the uptake of some radionuclides by Balck Sea macrophytes. Rapp. Comm. int. Mer Medit., 28, 7: 263-265 BOLOGA A.S., 1987-1988 – Annotated bibliography on the macrophytobenthos along the Romanian Black Sea coast (1881-1986) Cercetari marine, Recherches marines, 20 / 21, 353-384 BOLOGA A.S., 2001 – Destruction of marine biodiversity – a case study of the Black Sea. IOI – Pacem in Maribus XXVII Conference, Proceedings: 249-254 BOLOGA A.S., SAVA D., 2006 - Progressive decline and present trend of Romanian Black Sea macroalgal flora – Cercetari marine, Recherches marine, 36;31-60 CELAN M., 1935 - Notes sur la flore algologique du littoral roumain de la mer Noire. I. Sur les Cystoseira. Bull. Sect. Sci. Acad. Roumaine 17: 81-94 CELAN M., 1936 - Notes sur la flore algologique du littoral roumain de la Mer Noire. III.Quelques algues récoltées sur la portion du littoral „Institut Bio-océanographique du Constantza –Cap Midia Academie Roumaine – Mem. Sect. Sci. Romana 3:39-69 CELAN M., 1938 - Notes sur le flore algologique du littoral roumain de la Mer Noire V.- Quelques algues nouvelles pour la flore de la Mer Noire – Bull. Sci. Acad. Roumaine 20, 4-5: 84-89 CELAN M., 1940 - Recherches cytologiques sur les algue rouges. Thèse pour le Doctorat es Sciences naturelles, Botanique, Paris, 1940, 1-168, avec 7 planches hors texte, dont quatre en couleur CELAN M. - 1948 - Sur la végétation algale à Agigea (mer Noire) pendant les mois SeptembreNovembre 1946, Bull.Inst. Polytechn. Iassy 4:340-351 CELAN M., 1958 - Noi contributii la cunoaşterea florei şi vegetatiei Marii Negre –Analele Univ. „C.I. Parhon”, Bucuresti, seria St. Naturii, 17: 77-94 CELAN M., 1960 - Flora si vegetatia Marii Negre, in: Monografia Geografica a R.P.R. Geografia fizica, Ed. Academiei, Bucuresti, I: 584-585 CELAN M., SERBANESCU G., 1959- Sur les Ceramium de la mer Noire - Lucr. Ses. Sti. Stat. Zool. Mar. Prof. I. Borcea, Agigea: 531-56 CELAN M., BAVARU A., 1973 – Aperçu général sur les groupements algaux des côtes roumaines de la mer Noire. Rapp. Comm. Int. Mer Médit. 21, 655-656 CELAN M., 1977 - Sur l’appau-vrissement de la flore algae des côtes roumaines de la mer Noire – Hidrobiologia 15: 61-64 CELAN M., BAVARU A., 1978 – Sur l’état actual de la végétation algale du littoral Roumain de la mer Noire. Cercetari marine, Recherches marines, 11, 85-90 KANITZ A., 1881 – Plantas Romaniae hucusque cognitas, enumerat Augustus Kanitz: Algae auctore Julio Sachaarscmidt, Claudiopoli, 1878-1881, 151-268 SAVA D., 2002 – Impactul ecologic al poluarii asupra cenozelor de macrofite de la litoralul stancos al Marii Negre, Teza de doctorat, Universitatea “Ovidius” Constanta, 233 pp 69 25. SAVA D., ARCUS M., DOROFTEI E., BUSURICU F., BALABAN D.P., 2003 – The latest data on the qualitative structure of macrophytobenthos from the Romanian Black Sea shore. 4th Int. Conf. PH students, Miskolc, Hungary, 365-370 26. SKOLKA H.V., 1956 – Speciile de Phyllophora din apele romaneşti ale Marii Negre – raspandirea si importanta lor – Bul. Inst. Cercet. Piscicole,15, 4: 84-88 27. SKOLKA H.V., 1969 – A propos de la repartition des algue macrophytes la long de côte roumaine de la Mer Noire –Rev Roum. Biol. Ser. Bot., 14, 6:363-368 28. SKOLKA H.V., BODEANU N., 1971 – Les associations micro et macrovegetales de la partie de nordouest de la Mer noire – Rapp. Comm int. Mer Medit. 20, 3: 197-199 29. SKOLKA H.V., VASILIU F. BOLOGA A.S., 1980 – Les development des algue macrophytes le long du littoral roumain pendant les annees 1977-1978 – Cercetari marine, Recherches marine, 13: 135-142 30. TEODORESCU E.C., 1907 – Materiaux pour la flore algologique de la Roumanie, Beihefte Bot. Centralbl., 21, 2: 103-219. 31. VASILIU F., 1984 – Productia algelor macrofite de la litoralul românesc al Marii Negre, Teza de doctorat, Universitatea Bucuresti, 210 pp. 32. VASILIU F., 1996 – Unele consideratii ecologice asupra listei de specii macrofite prezente la litoralul romanesc al Marii Negre. Naturalia – Pitesti, St. cerc., II-III, 432-444. 33. ZINOVA A.D., 1967 – Opredeliteli zelenykh, burykh i krasnykh vodorosley iuzhnykh morey CCCP, Izd. “Nauka”, Moskva – Leningrad, 399 pp. 70 AMPHIBIANS AND REPTILES FROM THE BLACK SEA COAST AREA BETWEEN CAPE MIDIA AND CAPE KALIAKRA Dan COG LNICEANU, Ciprian SAMOIL , Marian TUDOR, Marius SKOLKA University Ovidius Constanţa, Faculty of Natural Sciences B-dul Mamaia, nr. 124, Constanţa, 900527, Romania, dcogalniceanu@univ-ovidius.ro __________________________________________________________________________________________ Abstract: We present a preliminary inventory of amphibian and reptile species along the coastline between Cape Midia (Romania) and Cape Kaliakra (Bulgaria). Eight amphibian species and nine reptile species were inventoried in the area. The inventory was not complete since the species accumulation curve did not reach the plateau, but the results can provide an useful baseline for a future monitoring program in the area. The two countries share many common environmental problems along the Black Sea coastline, but more efforts are required to integrate existing conservation and legislation measures into effective tools for biodiversity conservation. Keywords: inventory, amphibians, reptiles, species richness, distribution, mapping, geodatabase __________________________________________________________________________________________ Introduction The coastal area between Cape Midia and Cape Kaliakra belongs to the Pontic (Black Sea) bioregion and presents unique characteristics. It stretches along approximately 120 km and has been impacted by humans for thousands of years. The Romanian coastline has been transformed by urban, tourism and industrial development, with few parts left in a semi-natural state. The Bulgarian coastline is less stressed by human development; here there are few localities and tourist facilities and no industrial areas. The area covered by the present study does not only follow a North-South latitudinal gradient, but also a mosaic of human-impacted areas. Amphibians and reptiles are taxa that appeared and evolved during hundreds of millions of years, surviving several major extinction periods. Nevertheless, they are sensible to human impact and are good indicators of the state of the environment. Both amphibians (Stuart et al. 2004) and reptiles (Gibbons et al. 2000) are declining worldwide and are considered priority taxa for conservation (Gascon et al. 2007). Monitoring amphibian and reptile populations is recommended since they are sensible to even minor changes in the quality of their habitats (Dodd et al. in press). In the present paper we present a preliminary inventory of amphibian and reptile species along the coastline between Cape Midia (Romania) and Cape Kaliakra (Bulgaria), providing the baseline data for a future monitoring program in the area. Materials and Methods During April until August 2008 we conducted monthly field trips lasting four to five days each along the entire coastline. We used a combination of visual encounter, active search and dip-net sampling techniques to detect amphibians, as well as visual encounter and active search for reptiles. The geographical coordinates and altitude of each site were recorded with a handheld Garmin GPS device. We also recorded the characteristics of aquatic and terrestrial habitat (type, area, maxim depth, pH, conductivity, vegetation, presence of predators) and the human impact. Existing distribution data was based on Szekely et al. (in press) for the Romanian part, and on several publications covering the area of interest in Bulgaria (Lepşi 1926; 1927; 1929; Beschkov 1984a; 1984b; 1985). We did not consider the updated taxonomic nomenclature, such as the one proposed by Frost et al. (2006) for amphibians; instead we used the taxonomy still valid in the national legislations. We built an amphibians and reptiles geodatabase in order to manage the geographic distribution of species records and perform spatial queries. The spatial data originated in two main sources: GPS data collection from the inventory in 2008 and locality data extracted from bibliographic sources. 71 Both types of data were spatially joined to the UTM 5x5 km grid system based on the corresponding cell code attributes, and then exported as polygon feature classes and related attribute tables into a personal geodatabase. We performed the spatial analysis on species records and produced a series of maps with ArcGIS Desktop 9.3, using the ESRI Data and Maps 2008, and elevation Data from NASA, NGA, USGS as main basemap sources. The coordinate system used for each map was UTM Zone 35N, and datum: WGS 1984 (Figure 1). Figure 1 - The Black Sea coastal area between Cape Midia and Cape Kaliakra covered by the present study A species accumulation curve was computed for amphibians and reptiles based on individual site data (i.e. sample based) using EstimateS 7.5 (Colwell, 2005). Sample order was randomized 50 times and mean richness 72 estimates were computed for each sample accumulation level. This removes the effect of sample order and generates a smoother curve. Results and Discussion Amphibians and reptiles are widespread along the coastline, even in highly impacted areas. During our inventory we found individuals of eight amphibian species (Bombina bombina, Pelobates fuscus, Pelobates syriacus, Bufo viridis, Hyla arborea, Rana kl. esculenta, R. lessonae, R. ridibunda), and nine reptile species (Testudo graeca, Emys orbicularis, Lacerta viridis, L. trilineata, Podarcis taurica, P. muralis, Pseudopus apodus, Coluber caspius, Natrix natrix, Vipera ammodytes). Since the collecting effort differed between the two countries, we analyzed the data separately. The species accumulation curves based on the number of inventoried sites did not reach a plateau for both countries (Figures 2 and 3), indicating that the inventory was incomplete. This is normal for the two taxa where species detectability varies within a wide range. Some species (e.g. Pelobates sp., Eryx jaculus) are active only during the night, or possess cryptic coloration (e.g. Vipera ammodytes) and thus have a lower detectability Species richness 25 20 15 10 5 0 1 6 11 16 21 26 31 36 41 Number of localities Figure 2 – Species accumulation curve for amphibians and reptiles inventoried along the coastline between Cape Midia and Vama Veche (Romania). 73 Species richness 20 15 10 5 0 1 A. 3 5 7 9 11 Number of localities 10 Number of species 8 6 4 Bolata Dere Kaliakra 2 Durankulak 0 B. 1 2 3 4 5 Number of visits Figure 3 – A. Species accumulation curve for amphibians and reptiles inventoried along the coastline between Durankulak and Cape Kaliakra (Bulgaria). B. Species accumulation curve for three Bulgarian sites with high species richness according to the number of visits. 74 Some species were widespread and/or had a high detectability and were recorded from most sites and/or during each visit (Figure 4). This is the case for water frogs of the Rana esculenta complex and for the lizard Podarcis taurica and the tortoise Testudo graeca. Other species were rare, either limited to aquatic habitats (e.g. Emys orbicularis, B. bombina) or type of soil (e.g. Pelobates sp.). Rana esculenta complex Podarcis taurica Testudo graeca Podarcis muralis Lacerta viridis Hyla arborea Bufo viridis Pseudopus apodus Natrix natrix Dolicophis caspius Pelobates syriacus Bombina bombina Vipera ammodytes Emys orbicularis Lacerta trilineata 0 2 4 6 8 10 12 14 16 Number of sightings Figure 4 – Frequency of amphibians and reptiles based on the number of sightings along the Bulgarian coastline between Durankulak and Cape Kaliakra in 2008. The highest species richness was recorded in Bulgaria in sites that contained both terrestrial and aquatic habitats (Durankulak, Bolata Dere, Rusalka) while the sites without freshwater aquatic habitats had a lower species richness due to the absence of most amphibian species (Figure 5). Kaliakra Durankulak Bolata Dere Rusalka Zelenka Tuzlata Shabla Krapets Kamen Bryag Yaylata 0 2 4 6 8 10 Number of species Figure 5 – Relative species richness of amphibians and reptiles in several sites inventoried in Bulgaria in 2008. 75 The species richness pattern can not be correlated with human density, a high number of species being recorded also from urban or industrial areas (Figure 6). Overall, coastal areas with wetlands hold the highest species diversity, while the lowest is recorded from inland arid plains used mainly in agriculture, with or without irrigation. Figure 6 – Amphibian and reptile species richness along the coastline between Cape Midia and Cape Kaliakra. 76 The distribution of several amphibian and reptile species are presented below, including widespread species like Bufo viridis (Figure 7), Podarcis taurica (Figure 8), Natrix natrix (Figure 9), Dolicophis caspius (Figure 10), Testudo graeca (Figure 11), or species with specific habitat requirements and a more restricted distribution, like Bombina bombina (Figure 12), Hyla arborea (Figure 13) or Podarcis muralis (Figure 14). Figure 7 – Distribution of the Green Toad Bufo viridis along the coastline between Cape Midia and Cape Kaliakra. 77 Figure 8 – Distribution of the Balkan Wall lizard Podarcis taurica along the coastline between Cape Midia and Cape Kaliakra. 78 Figure 9 – Distribution of the Grass Snake Natrix natrix along the coastline between Cape Midia and Cape Kaliakra. 79 Figure 10 – Distribution of the Large Whip Snake Coluber caspius along the coastline between Cape Midia and Cape Kaliakra. 80 Figure 11 – Distribution of the Spur-thighed Tortoise Testudo graeca along the coastline between Cape Midia and Cape Kaliakra. 81 Figure 12 – Distribution of the Fire-bellied toad Bombina bombina along the coastline between Cape Midia and Cape Kaliakra. 82 Figure 13 – Distribution of the Tree Frog Hyla arborea along the coastline between Cape Midia and Cape Kaliakra. 83 Figure 14 – Distribution of the Wall lizard Podarcis muralis along the coastline between Cape Midia and Cape Kaliakra. 84 Several species have an even more restricted distribution in the studied area, reaching either their northern distribution limit (e.g. Ophisaurus apodus) or their southern limit (e.g. Eremias arguta) (Figure 15). Figure 15 – Distribution of the Steppe Runner Eremias arguta and the European Glass Lizard Ophisaurus apodus along the coastline between Cape Midia and Cape Kaliakra. 85 The amphibian and reptile fauna is similar for the coastline stretches of the two countries, despite the rather large differences between Balkan countries (Atatür and Yilmaz 1986). Bulgaria has a higher amphibian and reptile species diversity as compared to Romania, despite its smaller area (Table 1). The area covered by our study is relatively uniform relatively to the number of species, only two reptile species being present only in one country each (Eremias arguta in Romania and Pseudopus apodus in Bulgaria). Our inventory was not complete as indicated by the species accumulation curves. When comparing our results to the management plans for two protected areas in Bulgaria – Durankulak and Shabla the differences in species richness are significant. The species listed in the management plans are not based on inventories but on the coarse distribution of the amphibians and reptiles in Bulgaria. It is not backed by recent distribution maps (Gasc et al. 1997; Naumov and Stanchev 2008). For example, Trayanov (1996, unpublished report cited in the Draft Management Plan for Shabla Lake Complex in 1998) reports five amphibian and six reptile species in Shabla lake complex. For Kaliakra and Bolata Dere, the Draft Management Plan (1997) mentions 20 species, but the report is unreliable and does not refer to any bibliographic source. For example, it cites Triturus cristatus, which is not present in Bulgaria, clearly confusing it with T. karelinii, mentions B. variegata, confusing it with B. bombina, wrongly mentions Lacerta taurica and L. muralis, which belong to the genus Podarcis. The herpetofauna of Romania and Bulgaria differs in both species richness and percentage of species protected. The conservation status of amphibians and reptiles varies between the two countries (Table 1). While in Romania all species, except for Natrix natrix, are included in OUG 57/2007, in Bulgaria only 2/3 are included in the annexes (Law 77/2002). Table 1 – The number of species of amphibians and reptiles from Romania and Bulgaria and their conservation status. Romania also protects subspecies and they are represented in addition to the number of species preserved. PARAMETERS ROMANIA BULGARIA Surface (km2) 237,500 110,910 19+1 18 20 17 100% 94% 8 7 23+1 35 23 24 96% 68% 42+2 53 1.76/1.85 9.81 8 9 Amphibians (number of species) Protected by Habitats Directive (number) Protected by Habitats Directive (%) Number of amphibian species from the investigated coastline area Reptiles (number of species) Protected by Habitats Directive (number) Protected by Habitats Directive (%) Total number of species Species density (number of species/10,000 km2) Number of reptile species from the investigated coastline area A more detailed comparative analysis of the distribution and conservation status of amphibians and reptiles in the two countries is given in Tables 2 and 3. 86 Both countries share many environmental problems along the 170 km of terrestrial border in Dobrudja. Nevertheless there are many differences between the measures taken by the two governments in tackling environmental problems, starting from discrepancies in legislation and conservation status. Protecting the unique ecosystems and species diversity of the Black Sea Coast requires a higher degree of cooperation and joint measures, in a coherent approach. Table 2 - A comparative analysis of the conservation status of amphibians in Romania, Bulgaria and according to international conventions or IUCN Red List. The EU Habitats Directive (92/43/EEC) was implemented in Romania by OUG 57/2007 and in Bulgaria by Law 77/2002. The Romanian Red List is according to Botnariuc and Tatole (2005) and the Bulgarian according to Beschkov (1985). The species inventoried during the present study are marked with P. 87 Table 3 - A comparative analysis of the conservation status of reptiles in Romania, Bulgaria and according to international conventions or IUCN Red List. The taxonomy is according to national legislation; in four species different names are used in the two countries. The EU Habitats Directive (92/43/EEC) was implemented in Romania by OUG 57/2007 and in Bulgaria by Law 77/2002. The Romanian Red List is according to Botnariuc and Tatole (2005) and the Bulgarian Red List according to Beschkov (1985).The species inventoried during the present study are marked with P. 88 References 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19. ATATÜR, M.K., YILMAZ, I., 1986 - A comparison of the amphibian fauna of Turkish Thrace with that of Anatolia and Balkan States. Amphibia-Reptilia 7: 135-140. BESCHKOV, V., 1984 - On the Distribution, Relative Abundance and Protection of Tortoises in Bulgaria. Ekology, 14: 14-34. BESCHKOV, V., 1984 - The Effect of the Balkan Range on the Distribution of the Herpetofauna in Bulgaria. Acta zool. bulg., 25: 9-15. BESCHKOV, V., 1985 - Amphibia and Reptilia in Red Data Book of the P. R. of Bulgaria, Animals, 2: 32-41. BOTNARIUC, N., TATOLE, V. (Editors). 2005. Cartea Roşie a Vertebratelor din România. Academia Român /Muzeul Na ional de Istorie Natural “Grigore Antipa”. COLWELL, R. K., 2005 - EstimateS: Statistical estimation of species richness and shared species from samples. Version 7.5. User's Guide and application published at: http://purl.oclc.org/estimates. DODD, K.C., LOMAN, J., COG LNICEANU, D., PUKY, M. in press - Monitoring amphibian populations. Ch. 18. Amphibian Biology, vol. 8, Surrey Beatty & Sons. FROST, D.R., GRANT, T., FAIVOVICH, J., BAIN, R.H., HAAS, A., HADDAD, C.F.B., DE SA, R.O., CHANNING, A., WILKINSON, M., DONNELLAN, S.C., RAXWORTHY, C.J., CAMPBELL, J.A., BLOTTO, B.L., MOLER, P., DREWES, R.C., NUSSBAUM, R.A., LYNCH, J.D., GREEN, D.M., WHEELER, W.C., 2006 - The amphibian tree of life. Bull. Amer. Mus. Nat. Hist. 297: 1-370. GASC, J.P., CABELA, A., CRNOBRNJA-ISAILOVIC, J., DOLMEN, D., GROSSENBACHER, K., HAFFNER, P., LESCURE, J., MARTENS, H., MARTÍNEZ RICA, J.P., MAURIN, H., OLIVEIRA, M.E., SOFIANIDOU, T.S., VEITH, M., AND ZUIDERWIJK, A. (Editors), 1997 - Atlas of Amphibians and Reptiles in Europe. SEH, MNHN & SPN, Paris. GASCON, C., COLLINS, J. P., MOORE, R. D., CHURCH, D. R., MCKAY, J. E., MENDELSON, J. R. III (eds), 2007 - Amphibian Conservation Action Plan. IUCN/SSC Amphibian Specialist Group. Gland, Switzerland and Cambridge, UK. 64 pp. GIBBONS, J.W. SCOTT, D.E., RYAN, T.J., BUHLMANN, K.A., TUBERVILLE, T.D., METTS, B.S., GREENE, J.L., MILLS, T., LEIDEN, Y., POPPY, S., WINNE, C.T., 2000 - The Global Decline of Reptiles, Déjà Vu Amphibians . BioScience 50: 653-666. LEPŞI, I., 1926 - Ophisaurus apus Pall. neu für Rumänien. Verh. Mitt. Siebenb. Ver. Naturw. Hermannstadt. Sibiu, 75-76: 45-48. LEPŞI, I., 1927 - Beiträge zur Reptilien fauna der südöstlichen Dobrudscha. Verh. Mitt. Siebenb. Ver. Naturw. Hermannstadt. Sibiu, 77: 1-24. LEPŞI, I., 1929 - Despre fauna Dobrogei. Revista ştiin ific “V. Adamachi”, Iaşi, 2-3: 1-11. NAUMOV, B., STANCHEV, M., 2008 - Amphibians and reptiles in Bulgaria and Balkan Peninsula. An online edition of the Bulgarian Herpetological Society. Accessible at: http://www.geocities.com/herpetology_bg. STUART, S.N., CHANSON, I.S., COX, N.A., YOUNG, B.E., RODRIGUES, A.S.L., FISHMAN, D.L., WALLER, R.W., 2004 - Status and trends of amphibian declines and extinctions worldwide. Science 3: 1783-1785. SZÉKELY, P., PL IAŞU, R., TUDOR, M., COG LNICEANU, D. in press - The distribution and conservation status of amphibians in Dobrudja (Romania). Turkish Journal of Zoology. ***, 1998 - Shabla Lake Complex. Management Plan. Draft. Ministry of Environment & Waters BirdLife Switzerland Swiss Agency for Develpment & National Nature Protection Service /SVS/ Cooperation /SDC. Bulgaria, Varna. ***, 1997 - Kaliakra Reserve. Management Plan. Draft Ministry of Environment & Waters Swiss Agency for Develpment & National Nature Protection Service Co-operation /SDC/Bulgaria, 1997 INVERTEBRATE DIVERSITY IN THE WESTERN PART OF BLACK SEA COAST: CAPE MIDIA - CAPE KALIAKRA ZONE Marius SKOLKA Universitatea Ovidius Constanţa, Faculty of Natural and Agricultural Sciences, Dept. of Biology - Ecology Mamaia Bd. 124, Constanţa, 900527, Romania, mskolka@gmail.com ______________________________________________________________________________________ Abstract: The western littoral part of the Black Sea is characterized by a series of specific habitats, from the rocky cliffs covered with tree clusters to the marine dunes. The invertebrate fauna of these habitats is very interesting, characterized by a number of endemic species, specific to the Pontic province. The present paper succinctly presents the data known to the present day for the area between Cape Midia and Cape Kaliakra. These data represent the result of the research activities accomplished within the Program PHARE CBC RO2005/017535.01.02.02 which took place between April-August 2008. Key words: invertebrate diversity, Black Sea littoral, Romania, Bulgaria __________________________________________________________________________________________ Introduction The Black Sea littoral represents a special area from many points of view. The special ecotone conditions are practically unique compared to other types of habitats, while the fauna, as well as the littoral flora, is strongly influenced by the marine climate. The species present here – psamophylous, hygrophile or thalassophylous – even though found in considerable numbers in the neighboring areas as well (steppe vegetation or wetlands), form a particular association. Due to the narrow littoral area – a few hundred meters at most – the fauna associations – quite poor in species compared to those in the neighboring areas – are subject to much stronger anthropogenic pressure, any modification of the habitat leading to the disappearance of entire groups. Thus, the harbor developments on the one side, as well as the development of the specific touristic infrastructures on the other, have led to the disappearance of fauna encountered frequently on the beaches from large portions of the littoral (especially the area Mamaia-Eforie North). From an ecological point of view, several types of fauna groups can be found in the littoral area. If we classify these groups according to the microhabitats, the following categories can be counted: - The fauna of decomposing algae deposits and alluvial deposits; - The fauna of the beach proper, with no vegetation; - The fauna of psamophile vegetation with Crambe maritima, Salsola sp., Cakile maritima; - The fauna of the herbaceous vegetation strip dominated by Leymus sabulosus; - The fauna of the wetlands in the Vadu-Navodari area and the paramarine lake areas; - The fauna of the high seawalls in the southern part of the littoral. Among these particular types of fauna, those exclusive to the littoral area are the first four. Here, there is a number of typical species, while in the seawall fauna in the southern littoral and the wetland area north of Mamaia – more and more affected by the anthropogenic impact – the fauna is made up of species present in other types of habitats as well. A specification must be made from the very beginning. The studies effected on the fauna in the littoral area in general and the entomofauna in particular have been sporadic and, with the exception of the valuable researches of Carol Nagy (Nagy, 1971, 1972), they usually approached aspects regarding one or another of the taxonomical groups. Comparative ecological studies on these interesting insect groups lack almost completely. 90 Material and Methods The present paper is mostly based on specialized literature for the outlining of species into different taxonomic groups which occur in the littoral area. Also, the field observations within the Program PHARE CBC RO2005/017-535.01.02.02 between April-August 2008 completed the literature data for some of the insect groups. Results and Discussions The most interesting fauna group in the littoral area can be found in the vicinity of the wave breaking area, where algae debris or mollusk shells deposit all year round. All this decomposing debris represents a complex ensemble of habitat niches populated by an important number of living creatures. The trophic chains formed here are based on trophic resources of organic decomposing matter. Some of the species present in the detritus deposits can also be found in other areas, while other species are characteristic to a specific zone. Particularly interesting is the presence of certain marine species that consume the same resources in this narrow portion. Thus, in the alluvial deposits of the littoral area and under the piles of algae, one can frequently encounter gammarid amphipods, while crabs like Carcinus mediterraneus (quite rare over the last decades at the Romanian littoral) or Pachygrapsus marmoratus usually feed during the warm season with mollusk cadavers thrown on the beach by the waves, and not only. The fauna encountered in the organic detritus deposits on the beach is made up especially of insects, which dominate in terms of number of species and individuals. A number of birds specialized in exploiting the same habitat niches complete the fauna here. The insects encountered in this area are divided into several categories. A first category is represented by those species that consume decomposing organic matter. This category contains not only Dermaptera such as Labidura riparia (characteristic to the littoral area, where large populations can be found), springtails (Collembola) of the genera Entomobrya and Tomocerus, etc. but especially larvae and adults of brachycer Diptera and Coleoptera. Among these: Euconnus waterhali (Scydmenidae), Sapromyza bipunctata, Fucellia maritima (in large numbers on the beaches, even in warm days during the cold season), Choleva oblonga, Ptomaphagus varicornis, Sciodrepa watsoni, Catops tristis (Catopidae), Calobaea bifasciella, Ctenulus pectoralis, Salticella fasciata (Sciomyzidae), Pyrelia cadaverina, Piophila caripes (Piophilidae), Ephydra macellaria (whose larvae feed on epibiont Diatomea on the rocks in the wave breaking area or on decomposing vegetal remains), Lucilia sericata, Agyrtes castaneus, Necrodes littoralis, Ablataria laevigata (Silphidae), Lebia cyanocephala, Chlaenius festivus (Coleoptera). The larvae of some of these species often practice cannibalism – phenomenon also observed in Labidura. Also on the sea shore, one can encounter certain species of Heteroptera such as Prostemma gutula, Prostemma seneicole – which take shelter in mollusk shells, Prostemma sanguinea, Nysus senecionis – found on rocky beaches in the southern littoral, Tingis maculata, Aethus nigritus, found on sandy beaches in the north, Microvelia schneideri – on the piles of decomposing algae. Another category is represented by the carnivorous species that feed on larvae or adults of species in the first category or which they use as hosts. This group is made up especially of Coleoptera - Cicindela trisignata, Clivina fosor, Clivina ypsilon, Paederus riparius – or Hymenoptera genus – Teleas, Brachymeria (which are parasites for other species) and species Bembix oculata, Bembix olivacea (which feeds its larvae with different Diptera species captured on the detritus deposits on the beach), to which ants, Neuroptera or damselflies and dragonflies are added, but they are not as important. Certain birds that live on the beaches also feed on larvae of the different insect species that grow in the decomposing algae deposits. The beaches proper, deprived of vegetation, have a poor fauna, represented especially by species from the neighboring areas – the vegetation zone or the sea shore with alga or mollusk deposits. On the beaches, one may encounter especially predatory species that are active in open field – such as the Cicindelida among Coleoptera, certain species of Hymenoptera such as Pompilus plumbeus or Ammophila sabulosa, Heteroptera such as Aethus nigritus, Arma custos (which hunts other insect species), Saldula saltatoria, certain predatory Diptera in the Asilida group, the spiders. More rarely, during the night, certain large Myriapoda can be found in the same area – Scolopendra cingulata, while during the day, sand lizards venture in the area – Eremias arguta deserti. 91 In the psamophile vegetation areas with Crambe maritima and Cakile maritima, as well as in the area with Elymus sabulosus, the fauna is richer. On the bushes of Cakile maritima or Crambe maritima one can often find individuals of Heteroptera, some common like Eurydema ornata, but this is also where Eurydema spectabile is encountered, a species strictly localized on the littoral strip and which does not exist in other habitats; important populations of this species also occur on bushes of Crambe in the northern littoral. Grasshopers (Orthoptera) are also represented by common species, often in large numbers – Calliptamus italicus, Stenobothrus fischeri, Oedipoda germanica, but also by species strictly localized on the littoral strip, like Acrotylus longipes, species existing only in this type of habitat. The populations of this species have disappeared in the Mamaia-Agigea area, while it is rare in the southern littoral. An isolated population remains only in the Agigea sand dunes reservation, in the area with Convolvulus persicus; vigorous populations can be found north of Mamaia. Other species found in these areas: Gasteropoda/Gastropoda – Helicella obvia, Odonata – species of Agrion, Sympetrum, Ischnura pumilio, Orthoptera – Tetrix subulata, etc., Mantodea – Ameles decolor, seldom Mantis religiosa, Neuroptera, Heteroptera – Menccarus arenicola, Psacasta neglecta, Zicrona coerulea, Eysacoris punctatus, etc., Coleoptera – Lophyridia lunulata, Zbrus, Harpalus, Pogonidium laticolle, a large number of adults of species of Diptera, Hymenoptera – Ammophila sabulosa, Pompilus plumbeus, Bembix, Myrmecocystus. Vertebrate species can also be encountered in the area – reptiles (Eremias arguta deserti, Podarcis taurica) or birds that sometimes nestle in these habitats. The swampy areas are the richest in regards to the fauna, the following being dominant: Orthoptera – Tettigonia viridissima, Calliptamus italicus, Oedipoda coerulescens, Acrida hungarica – in areas where herbaceous vegetation dominates and the soil is not swampy, Nematocera Diptera the group of Chironomidae – Chironomus plumosus, C. salinarius, Glyptotendipes sp. and Culicidae – Culex sp., Aedes sp., Heteroptera (both the hydrocorisae Nepa, Ranatra, Notonecta, Plea, etc. - and geocorisae) and Lepidoptera – Lycaena phlaeas, Lycaena dispar. Well represented are also all types of insects with aquatic larvae or adults – Odonata of all genera (Callopteryx, Agrion, Lestes, Sympecma, Sympetrum, Ischnura, Aeschna, s.a.), Ephemeroptera – Caenis, Baetis, Ephemera), Coleoptera, etc. Still, the fauna of these habitats is not exclusive to the littoral area, as they are usually found around ponds and in Danube Delta and Danube Valley. The largest areas of this kind can be found north of Vadu-Mamaia, as in the southern littoral they are restricted to the seashore between Eforie South and Costinesti, where fresh water infiltrations occur at the basis of the seawalls and this permits the development of compact bushes. They are also restricted to the Hergheliei Swamp near Mangalia. The southern littoral with high seawalls partially covered by sparse vegetation represents another interesting habitat. The seawalls position makes them directly influenced by the salty marine moisture and by the strong sunlight. The vegetation living here is mostly of steppe origin. The particular importance of these habitats comes from the fact that the littoral steppe is almost entirely gone, being limited to a very narrow strip on the superior part of the seawalls, the rest being occupied by agricultural crops. The seawall entomofauna is also mostly represented by steppe species that take shelter in the vegetation from the edge of the seawalls or on that of the steep slopes, or it is made up of species that visit flowing plants in these narrow strips of wild vegetation. This justifies the exhaustive citation of all the taxa encountered in this area. There are frequent Odonata – Sympecma fusca, Sympetrum vulgatum, Aeschna affinis, Mantidae – Mantis religiosa, Orthoptera – Gryllus desertus, Poecillimon brunneri, Isophya speciosa, Saga pedo (very rare), Tetrix subulata, Calliptamus barbarus, Calliptamus italicus, Oedipoda sp., Acrida hungarica, Tettigonia viridissima, Phaneroptera falcata, Heteroptera – Metopoplax origani, Reduvius personatus, Anthocoris nemorum, Liocoris tripustulatus, etc, Homoptera – Centrotus cornutus, Cercopsis sanguinolenta, Neuroptera Chrysopidae and Myrmeleontidae, Coleoptera – Calosoma inquisitor, Notiophilus palustris, Bledius furcatus, a large number of species of Lepidoptera that visit flowering plants – Pontia daplidice, Colias croceus, Colias erate, Polyommatus icarus, Vanessa cardui, Vanessa atalanta, Argynnis lathonia, Coenonympha pamphilus etc, adults of Diptera that fly on the beach too, Hymenoptera. Among the Gasteropoda/Gastropoda?, quite frequent are Zebrina varnensis, Helicella obvia dobrudschae, Cernuella virgata variabilis, Helicopsis striata, Monacha carthusiana, among the Myriapoda Lithobius 92 forficatus, Scolopendra cingulata, Scutigera cleoptrata, order Araneae with families Lycosidae and/or Salticidae. The list of taxa in the Romanian littoral area Gasteropoda - Pulmonata Snails are poorly represented in the littoral areas (Grosuu, 1983, 1987, 1993; Negrea, 1994a, 1994b). The absence of vegetation on the beaches, as well as the influence of salt in the soil have caused the lack of Gasteropoda in the littoral strip. Numerous populations of Helicella or Zebrina varnensis can be encountered in the psamophile vegetation or the herbaceous areas on seawalls. In areas with swamp vegetation situated north of Mamaia, a number of aquatic or water loving species can occur. Similarly, in areas with trees or shrubs nearby the seashore, characteristic Gasteropoda occur. Zebrina varnensis Pfeiff. Milax dobrogicus Grossu Ovatella ( Myosotella) myosotis (Drap.) Cernuella virgata variabilis (Drap.) Lymnaea stagnalis (L.) Cernuella dobrogica Grossu Galba truncatula (O.F.Muller) Helicella obvia dobrudsche Clessin Ancylus fluviatilis (O.F.Muller) Helicella spiruloides Wagner Planorbis carinatus (Muller) Helicopsis striata O.F.Muller Planorbis planorbis (L.) Helicopsis dejecta Cristofori et Jan Zebrina varnensis (Pfeiff.) Helicopsis krynickii (Andr.) Chondrula tridens (O.F.Muller) Helicopsis derbentina (Krynicki) Cecilioides acicula (O.F.Muller) Cochlicella acuta (O.F.Muller) Oxychilus glaber (West) Monacha cartusiana (O.F.Muller) Oxychilus dilus rumelicus (Hesse) Helix pomatia L. Multidentula ovularis (Olivier) Helix lucorum O.F.Muller Milax kusceri H.Wagner Myriapoda – Chilopoda Millipedes and centipedes are poorly represented in the coastal habitats(Matic, 1966, 1992; Negru, 1994). Their ecological characteristic are often improper for most Myriapoda species. Still, some species can be present nearby beaches and mostly in the vegetation of high seawalls, the most frequent being Scolopendra cingulata and Scutigera cleoptrata. Lithobius forficatus (L.) Lithobius muticus Koch Lithobius (Monotarsobius) crassipes Koch Lithobius (Monotarsobius) burzenlandicus euxinicus Prunescu Scutigeromorpha Scutigera cleoptrata (L.) Scolopendra cingulata L Araneae The spiders are a little studied group in the Romanian littoral area and not only (Fuhn, Gherasim, 1995; Fuhn, Niculescu-Burlacu, 1971; Oltean, 1968). Due to the complexities of the trophic relationships in which they are involved as a group of predators, a systematic inventory of this group is absolutely necessary in the future. Lycosidae Arctosa cinerea Fabr. Pardosa italica Tong. Lycosa vultuosa Koch Pardosa luctinosa Simon Lycosa radiata Latr. Alopecosa cursor Hahn Salticidae Alopecosa sulzeri Pv. Yllenus horvathi Chyz. 93 Euophrys erratica Walck. Heliophanus flavipes Hahn. Heliophanus kochi Simon Marpissa muscosa Clerck Sitticus dzieduszyckii Koch Myrmarachne formicaria de Geer Insecta Ord. Collembola Springtails are a group that has few demands regarding the environment conditions, they often occur in large agglomerations in the littoral area, sometimes in particular microhabitats, such as the ponds remaining on rocks after storms, where hundreds of individuals can be found. The springtail fauna in the littoral area has not yet been studied systematically. Anurida maritima Guerin Archisotoma besselsi (Pacard) Entomobrya marginata Tulb. Friesea acuminata Denis Heteromorus major Mon. Onychiurus fimata Gisin Tomocerus vulgaris (Tullb.) Seira ferrari Parona Sminthurus sp. Ephemeroptera The larvae of Ephemeroptera are part of the pond fauna in the littoral area, while the adults occur in the entomofauna of herbaceous vegetation (Bogoescu, 1958). They are not present on the high seawalls in the southern littoral or on beaches. In the littoral area, only a few species can be found that also occur nearby fresh water habitats. Palingenia longicauda (Olivier) Ephemera vulgata L. Caenis horraria (L.) Baetis bioculatus (L.) Cloeon dipterum (L.) Odonata Damselflies and dragonflies are predatory species and good fliers and they can be found frequently on beaches or in habitats in their vicinity, especially where there are ponds or swamps nearby(Bulimar, 1992, 1993; Cârdei, Bulimar, 1963; Griebler, 1994) Anisoptera Libellula quadrimaculata L. Orthetrum cancellatum (L.) Sympetrum pedemontanum Allioni Sympetrum depressiusculum (Selys) Sympetrum sanguineum L. Aeschna grandis (L.) Aeschna affinis Steph. Anax imperator (Leach) Zygoptera Callopteryx splendens L. Agrion pulchellum (van der Linden) Lestes barbarus (van der Linden) Lestes viridis (van der Linden) Lestes dryas (Kirby) Sympecma fusca Lind. Agrion puella L. Ischnura pumilio Charp. Ischnura elegans Lind. Orthoptera Grasshoppers are one the groups represented especially in areas with herbaceous vegetation nearby beaches or on seawalls (Knechtel, Popovici-Baznosanu, 1950). Few species are adapted exclusively to the habitats with sparse psamophile vegetation like Acrotylus longipes with vigorous populations in the areas of Vadu-Mamaia and Eforie; the Agigea population, restricted to the sandy perimeter with Convolvulus persicus is currently endangered. 94 Tettigonioidea Tettigonia viridissima (L) Poecillimon brunneri Friv. Isophia speciosa Friv. Phaneroptera falcata Scop. Saga pedo Pall. Grylloidea Gryllus desertus (Pallas) Oecanthus pellucens Scop. Gryllotalpa gryllotalpa (L) Acridoidea Tetrix subulata L. Calliptamus italicus (L) Acrida hungarica (Herbst) Stenobothrus fischeri Ev. Oedipoda germanica Latr. Oedipoda coerulescens (L) Acrotylus longipes Charp. Blattodea Roaches occur accidentally in the littoral area. One of the species – Ectobius laponicus – is characteristic to forests and can be found only in areas with trees (Comorova Forest), while the other species prefer human presence and can be found in areas with buildings. An interesting situation is given by Periplaneta americana – a species that has immigrated recently and that has been appearing frequently since 1990 around Constanta, all year round. Ectobius laponicus L. Phyllodromia germanica L. Blatta orientalis L. Periplaneta americana L. Mantodea Praying mantids are poorly represented in the European entomofauna. Only two of the four species of Mantida (characteristic to Dobrogea) occur in the littoral areas with high seawalls (Knechtel, PopoviciBaznosanu, 1950). Mantis religiosa (L) Ameles decolor (Charp.) Dermaptera Polyphage species by excellence, Dermaptera (earwings) are one of the groups characteristic to beaches. The piles of decomposing algae or bivalves and crustaceans represent a trophic niche where Labidura riparia in particular, develop extremely numerous populations along the entire littoral. Forficula auricularia (L.) Labidura riparia Pall. Anechura bipunctata F. Chelidurella acanthopygia Gen. Thysanoptera The trips are distributed in areas with herbaceous vegetation and they are rare or absent on the beaches with sparse vegetation. The adults and the larvae occur in plant inflorescences. As with other groups, a systematic inventory of Thysanopterae in the littoral areas does not exist yet (Knechtel, 1951; Vasiliu-Oromulu, 1992, 1998). Taeniothrips frici Uzel Terebrantia Thrips tabaci (Lindeman) Aelothrips intermedius Bag. Stenothrips graminum (Uzel) Aelothrips astutus (Priesner) Limothrips angulicornis Jab. Tubulifera Haplothrips angusticornis Priesner Pseudocryptothrips meridionalis (Priesner) Haplothrips reuteri Karny Haplothrips tritici Kurd. Kakothrips robustus (Uzel) Bolothrips icarus Uzel. Taeniothrips discolor (Karny) Bolothrips bicolor (Heeger) Heteroptera Heteroptera (bugs) – particularly their representatives of the order Gymnocerata, are one of the numerous groups in the terrestrial littoral biotopes. Unlike coleoptera or Diptera, Heteroptera populate the beach strips with herbaceous vegetation and especially the seawalls or the steppes nearby beaches. The special particularities of their eating habits do not permit them to occupy the trophic niches offered by the decomposing organic material on the beaches. Criptocerata can be found only in the ponds nearby the littoral or in the paramarine lakes (Kis, 1985, 1993 ; Schneider, Plattner, 1968). Cryptocerata Derula flavoguttata M.R. Corixa punctata Illiger. Carpocoris mediterraneus (Tamanini) Hesperocorixa linnaei Fieb. Carpocoris pudicus Poda Carpocoris fuscipinus Boh. Peracorixa coccinea Fieb. Antheminia lunulata Goeze Sigara stagnalis pontica Jacz. Palomena prasina L. Sigara assimilis Fieb. Eurydema ornata L. Sigara striata L. Eurydema spectabile (L) Sigara iactans Jann. Eurydema ventrale (Kolenati) Sigara lateralis Leach Menaccarus arenicola Schltz. Plea lechi McGreg. et Kirk. Sciocoris sulcatus Fieber Notonecta glauca L. Sciocoris helferi Fieber. Ilyocoris cimicoides L. Nepa rubra L. Sciocoris deltocephalus (Fieber) Ranatra linearis L. Sciocoris macrocephalus Fieb. Gerris lacustris L. Dryoderes umbraculatus Fabr. Gerris odontogaster Zett. Aelia acuminata L. Gerris argentatus Schum. Neotiglossa pusilla Gmel. Hydrometra stagnorum L. Holcostethus sphacelatus Fabr. Gymnocerata Zicrona coerulea L. Stibaropus henkei Jak. Arma custos F. Byrsinus fossor Mulss. et Rey Jalla domosa L. Aethus nigritus F. Troilus luridus F. Aethus flavicornis (Fabricius) Eysacoris punctatus L. Geotomus punctulatus (Costa) Henestaris halophilus Bur. Geotomus caucasius (Kolenati) Lygaeosoma reticulatum H.-S. Cydnus atterimus Frst. Nysus punctipennis H.-S. Legnotus limbosus (Geoffroi) Nysus thymi Wlff. Legnotus picipes Fall. Nysus senecionis Schill. Canthophorus melanopterus H.- S. Metopoplax origani Kolenanti Schirus morio L. Derephysia foliacea Fall. Odontoscelis lineola (Rambur) Stephanitis piri Geoff. Odontoscelis dorsalis (Fabricius) Tingis maculata H.-S. Odontoscelis fuliginosa L. Reduvius personatus L. Irochrotus lanatus (Pallas) Prostemma guttula F. Prostemma seneicolle Stein Phimodera humeralis (Dalman) Prostemma sanguinea Rossi Psacasta neglecta H.-S. Hebrus pusillus Fall. Psacasta exanthematica (Scopoli) Nabis apterus F. Eurygaster austriaca (Schrank) Nabis ferus L. Eurygaster itegriceps (Puton) Nabis brevis Schltz. Eurygaster maura (L) Microvelia schneideri Schltz. Ancyrosoma leucogrammes Gmel. Velia currens F. Graphosoma lineatum L. 96 Saldula saltatoria L. Anthocoris nemorum L. Orius nigra Wlff. Orius minuta L. Capsodes gothicus L. Liocoris tripustulatus F. Camptobrochis punctulatus Fall. Codophila varia (Fabricius) Homoptera Homoptera represent another order that lacks data regarding the littoral areas. Entire taxonomic groups such as the suborder Auchenorhyncha are practically not studied. The aphids, for example, a very important group in the habitats with herbaceous vegetation can offer many interesting surprises. Centrotus cornutus F. Caliscelis bonellii Latr. Cercopsis sanguinolenta L. Neuroptera Both the adults and the larvae are predatory species. Coniopterigida and Chrysopida occur especially in areas with thick or bushy herbaceous vegetation, or in the biotopes where there are trees as well. Ant lions (Myrmeleonidae), on the other side, are by excellence inhabitants of the open biotopes, with soil that is relatively poorly covered by vegetation; their larvae prefer sandy soils on the beaches or in their close vicinity, where they build characteristic traps. The adults can be encountered in the herbaceous vegetation nearby the beaches (Kis et al, 1970). Coniopterygidea Chrysopa phyllochroma (Wesmael) Coniopteryx borealis (Tjeder) Coniopteryx loispetsederi (Aspock) Myrmeleonoidea Coniopteryx esbenpeterseni Tj. Dendroleon pantherinus (Fabr.) Coniopteryx tjederi Kimm. Megistopus flavicornis (Rossi) Hemerobiidea Creoleon lugdunense Villers Hemerobius humulinus L. Myrmeleon formicarius (L) Hemerobius stigma Steph. Myrmeleon inconspicuus (Rambur) Hemerobius micans Oliv. Euroleon nostras (Fourcroy) Aleuropteryx ornata (Kis) Acanthaclisis occitanica (Villers) Chrysopydea Acanthaclisis baetica (Ramb.) Chrysopa carnea Steph. Myrmecaelurus trigrammus (Pallas) Chrysopa hungarica (Klapalek) Neuroleon nemausiensis (Borkhausen) Chrysopa abbreviata (Curtis) Formicaleon tetragrammicus F. Chrysopa commata (Kis-Ujhelyi) Coleoptera Coleoptera represent one of the best represented groups on the beaches and in the littoral areas, alongside diptera (Crisan, 1993 ; Ienistea, 1968; Nitu, 1992; Ostafciuc, 1994; Panin, 1955; Panin, Savulescu, 1961; Popovici, 1992; Ruic nescu, 1995; Serafim, 1993°, 1993b; Serafim, Ruic nescu, 1995; Teodor, 1993; Teodor, Traian, 1996). Among Coleoptera, a large number of species literally consume – as adults or as larvae – the remains of decomposing algae on the beach; other species are saprobic, coprophage or necrophage, while others are carnivorous, attacking mostly Diptera larvae. Considering that the group befitted from detailed studies at national level, the species in the littoral area are relatively well known, too. Cicindella trisignata Dej. Carabus violaceus L. Cicindella campestris pontica Motsch. Calosoma inquisitor L. Cicindella lunulata nemoralis O. Calosoma maderae auropunctatum Hbst. 97 Oxytelus complanatus F. Stenus ater Mannh. Euplectes bicolor Denny Hister sinuatus Illig. Hister quadrimaculatus L. Hister fimetarius Hbst. Hister stercorarius Hoffm. Hister quadrinotatus Scriba Thanatophilus sinuatus F. Agyrtes castaneus Payk. Necrodes littoralis L. Silpha orientalis Brull. Silpha carinata Illig. Drilus concolor Ahr. Choleva oblonga Mull. Ptomaphagus varicornis Rosh. Scioderpa watsoni Spin. Catops tristis Panz. Dermestes lardarius L. Dermestes mustelinus Er. Attagenus piceus Oliv. Anthrenus pimpinellae F. Anthrenus scrophulariae L. Anthrenus fuscus Oliv. Atomaria ruficornis Marsh. Heterocerus flexuosus Steph. Scymnus apetzi Muls. Phyllotreta poeciloceras Cond. Cryptocephalis globicollis Sufr. Cryptocephalus flavipes F. Cryprocephalus bipunctatus L. Crepidodera helxines L. Apthona cyparissiae Koch. Epicauta verticalis Illig. Zonitis caucasica Pall. Lydus balcanicus Steutz. Lydus chalybaeus Tautsch. Trichodes quadriguttatus Adams Notoxus trifasciatus Rossi Anthicus hispidus Rossi Anthicus antherinus L. Anthicus fenestratus Schm. Anthicus humilis Germ. Onthophagus lucidus Sturm. Potosia fieberi Kr. Epicometis hirta Poda Scarabaeus affinis (Brulle) Aphodius lugens (Creutzer) Aphodius punctipenis (Erichson) Omophron limbatum F. Clivina fossor L. Clivina ypsilon Dej. Dyschirus numidicus ponticus Lutshn. Brachinus explodens Duft. Brachinus crepitans L. Brachinus angustatus Dej. Polystichus conexus Fourc. Notiophilus palustris Duft. Ditomus capito Serv. Lebia cyanocephala L. Chlenius festivus F. Amara similata Gil. Amara familiaris Duft. Amara aenea De Geer Amara equestris Duft. Trechus quadristriatus Schrk. Microlestes minutullus Goeze Microlestes plagiatus Duft. Calatus cisteloides Panz. Calatus fuscus F. Zabrus blaptoides Creutz. Zabrus curtus Dej. Harpalus aeneus F. Harpalus azureus F. Harpalus serripes Luc. Harpalus distinguendus Luc. Bembidium varium Oliv. Pogonidium laticolle Duft. Pardileus calceatus Duft. Lyperosomus aterrimus Hbst. Staphylinus cesareus L. Staphylinus murinus L. Paederus riparius L. Carpelinus memnonius Kiesw. Philonthus fulvipes F. Philonthus punctatus Grav. Philonthus longicornis Steph. Philonthus xantholoma Grav. Tachyporus nitidulus F. Tachyporus obtusus L. Tachyporus chrysomelinus L. Conosoma pubescens Grav. Oxyporus rufus L. Troglophloeus riparius Boisd. Bledius tricornis Hbst. Bledius furcatus Oliv. Bledius unicornis Germ. Haploderus caelatus Grav. 98 Maladera holoserica Scop. Homaloplia alternata Kust. Homaloplia ruricola F.. Homaloplia erythroptera Friv. Coccinela septempunctata L. Thea 22-punctata L. Calamobius filum L. Aphodius immunus (Creutzer) Trox hispidus (Pontoppidan) Pentodon bidens (Pallas) Pentodon idiota Herbst. Polyphylla fullo (L.) Anoxia orientalis (Kryn) Anomala errans (Fabr.) Mecoptera This order – that includes scorpionflies - It is represented by a single species – Panorpa communis L. – rarely on the beach, sometimes close to wetlands (Nagler, 1968). Trichoptera The members of this group are relatively rare on the beaches. However, the adults can sometimes be found in large numbers in the herbaceous vegetation of the high seawalls in the south or close to the moors in the area of Vadu-Navodari. Also, they can be present in the anthropic areas along the littoral, if there are permanent ponds nearby (Ciubuc, 1993). Argypnia varia (Fabricius) Limnephilus flavospinosus (Stein) Limnephilus affinis Curtis Limnephilus sparsus Curtis Limnephilus bipunctatus Curtis Colpotaulius incistus (Curtis) Limnephilus decipiens (Kolenati) Oecetis ochreacea (Curtis) Lepidoptera Moths and butterflies are less connected to the beach biotope, where the larvae do not find a variety of trophic resources. However, the adults can be encountered both on the beaches, where they visit the flowers of rare psamophile plants, but especially in the areas with herbaceous vegetation or bushes close to the beaches. Also, the presence of forested areas close to the seashore, such as Comorova or Neptun, facilitate the presence of forest species in the littoral area (Kovacs et Kovacs, 1998, 1999; Rakosy, 1997; Rakosy, Szekely, 1996; Rusti, 1992, 1994; Skolka, 1994; Vicol, 1997). Triodia amasinus dobrogensis Car. Tineidae Euplocamus ophisus Cram. Cossidae Phragmataecia castanea Hb. Anemopogon quercicolellus H.-S. Parahypopta caestrum Hb. Neurothaumasia ankerella Mn. Zygaenidae Tinea pellionella L. Zygaena contaminei Bsdv. Tinea flavescentella Haw. Adscita subsolana Stgr. Fermocelina inquinatella Zell. Adscita globulariae Hb. Trichophaga tapetzella L. Adscita mannii Led. Trichophaga abruptella Wall. Monopis imella Hb. Geometridae Cyclophora porata L. Monopis nominella Zag. Scopula tesselaria Bsdv. Ethmiidae Ethmia bipunctella F. Scopula turbidaria Hb. Aegeriidae Scopula marginepunctata Goeze Chamaesphecia anellata (Zeller) Scopula beckeraria Led. Chamaesphecia astatiformis (Herrich Scopula incanata L. Schaffer) Scopula laevigata Scop. Chamaesphecia empiformis (Esper) Scopula flaccidaria Zel. Paranthrene tabaniformis (Rottenburg) Idaea vulpinaria H.-S. Idaea filicata Hb. Hepialidae 99 Idaea levigata Scop. Idaea camparia H.-S. Idaea elongaria Ramb. Idaea biselata Hfn. Idaea politata Hb. Idaea seriata Schr. Idaea degeneraria Hb. Rhodostrophia vibicaria Clerck. Caclysme riguata Hb. Lythria purpuraria L. Lythria purpurata L. Orthonoma obstipata F. Catarhoe rubidata D. et S. Epirrhoe galiata D. et S. Epirrhoe rivata Hb. Pelurga comitata L. Euphitecia insigniata Hb. Euphitecia variostrigata Alph. Eupithecia centaureata D. et S. Euphitecia breviculata Donz. Euphitecia denticulata Treitsche Euphitecia extensaria Fr. Euphitecia simpliciata Haw. Gymnoscellis rufifasciata Haw. Anaitis plagiata L. Lithostege duplicata Hb. Lomaspilis marginata L. Ligdia adustata D. et S. Semiothisa glarearia Brahm. Semiothisa aestimaria sareptanaria Stgr. Narraga tessularia kasyi Mouch. et Pov. Tephrina murinaria F. Tephrina arenacearia D. et S. Gnopharmia stevenaria Bsdv. Eilicrinia trinotata Metz. Apocheima pilosarium D. et S. Biston stratarius Hfn. Agriopis bajaria D. et S. Dasycorsa modesta Stgr. Peribatodes rhomboidaria D. et S. Peribatodes secundaria D. et S. Synopsis sociaria Hb. Boarmia roboraria D. et S. Serraca punctinalis Scop. Ascotis selenaria D. et S. Campaea margaritata L. Aspitates ochrearius Rossi Boarmia selenaria (Schiffer) Calothysanis amata (L.) Cidaria bilineata (L.) Lasiocampidae Gastroparca quercifolia L. Odonestis pruni L. Notodontidae Phalera bucephala L. Cerura vinula L. Dicranura ulmi D. et S. Paradrymonia vittata bulgarica de Freina Pterostoma palpinum Cl. Arctiidae Pelosia obtusa H.-S. Lithosia pallifrons Z. Lithosia quadra L. Eilema sororculum Hfn. Eilema caniola Hbn. Eilema pygmaeola Dbld. Coscinia striata L. Chelis maculosa mannerheimii Dup. Phragmatobia fuliginosa L. Spiris striata L. Spilosoma lubricipedum L. Spilosoma urticae Esp. Arctia caja L. Arctia villica L. Ammobiota festiva Hfn. Dysauxes famula pontica Frise Noctuidae Xestia c - nigum (L.) Dysgonia algira (L.) Agrostis ipsilon (Hufnagel) Trachea atriplicis (L.) Prodotis stolida (Fabr.) Emmelia trabealis (Scopoli) Autographa gamma (L.) Autographa confusa (Stephens) Mythimna albipuncta (Denis Schiffermuler) Heliothis maritima (Graslin) Lacanobia oleracea (L.) Catocala elocata (Esper) Catocala puerpra (Giorna) Sphingidae Acherontia atropos (L.) Herse convolvuli (L.) Smerinthus ocellata L. Laothoe populi L. Celerio lineata livornica Esp. Celerio euphorbiae L. 100 Pergesa elpenor L Pergesa porcelus (L.) Macroglosum stellatarum (L.) Hesperiidae Ochlodes venatus (Brem - Grey) Charcharodus flocciferus (Zell) Pyrgus serratulae. (L) Maniola jurtina (L.) Melanargia galathea (L.) Coenonympha pamphilus (L.) Lycaenidae Lycaena phlaeas (L.) Lycaena dispar L. Plebejus idas (L.) Plebejus argus (L.) Plebejus argyrognomon (Bgstr) Celastrina argiolus L. Polyommatus icarus (Rott) Aricia agestis (Schiff) Nymphalidae Nymphalis polychloros (L.) Aglais urticae (L.) Polygonia c - album (L.) Vanessa atalanta (L.) Vanessa cardui (L.) Inachis io (L.) Melitaea varia (Mey - Dun) Melitaea trivia (Den et Schifer) Melitaea phoebe (Schiff) Argynnis lathonia (L.) Argynnis pandora (Den et Schiff) Papilionidae Iphiclides podalirius (L.) Papilio machaon (L.) Pieridae Leptidea sinapis (L.) Anthocaris cardamines (L.) Pontia daplidice (L.) Pieris brassicae (L.) Pieris napi (L.) Pieris rapae (L.) Colias croceus (Fourcr.) Colias erate Esp. Gonepteryx rhamni (L.) Satyridae Pararge megaera (L.) Pararge maera (L.) Diptera Flies and mosquitos are relatively well represented in all the littoral areas (Albu, 1980; Ceianu 1999; Dinulescu, 1958; Ionescu, Weinberg, 1960, 1963, 1971; Neacsu, 1965; Pârvu, 1993a, 1993b, 1993c; Weinberg, 1994). The most frequent are brachycer Diptera, whose larvae feed on the piles of decomposing algae or on the cadavers of mollusks, crustaceans, fish and sometimes mammals and birds thrown on the beach by waves. A considerable number of this kind of species are characteristic to the beaches, and they can be found in numerous populations over the entire length of the littoral. Nematocera Diptera reach the beach accidentally; numerous populations of Chironomida and Culicida can be found in the north – Vadu-Navodari – or the Herghelie Swamp area in Mangalia, where there are swampy biotopes (where the larvae of these species develop) in the immediate vicinity of the beaches. Leptochironomus tener Nematocera Dicrotendipes fusconotarsus Kieff. Glyptotendipes barbipes St. Tipulidae Glyptotendipes severinei Goet. Endochironomus tendens Fabr. Tipula oleracea.L. Polypedilum nubeculossum Meig. Chironomidae. Polypedilum scalaenum Schr. Chironomus gr. plumosus Tanytarsus excavatus Edw. Chironomus halophilus Kieff. Paratanytarsus inoperatus Walk. Chironomus salinarius Kieff. Culicidae Einfeldia disidens Walk. Aedes caspius Pall. Haliella noctivaga Kieff. Aedes dorsalis Meig. Cryptocladopelma virescens Meig. Aedes cantans Meig. Parachironomus arcuatus Goet. 101 Aedes salinus Edw. Aedes quartus Mart. Aedes geniculata Edw. Culex pipiens pipiens L. Culex pipiens molestus Forsk. Culex modestus Fic. Culex tipuliformis Theobald Urotaenia unguiculata Edw. Taniorhynchus richardii Fic. Anopheles maculipennis Meig. Anopheles pseudopictus Grasse Anopheles bifurcatus L. Anopheles messeae Fall. Anopheles labranchiae Fall. Anopheles hyrcanus Pall. Brachycera Laphria fulva Mg. Compsilura concinnata Mg. Siphona geniculata De Geer Monoleta cincta Nees Limnobia nubeculosa Mg. Erioptera trivialis Mg. Limnophila oleracea Mg. Bibio marci L. Sciara thomae L. Scatopse fuscipes Mg. Hermione trilineata F. Haplodonta viridula F. Rhagio lieneola F. Chrysops flavipes Meig. Chrysops italicus (Meigen) Chrysops pictus Meig. Tabanus solstitialis Mg. Tabanus lunatus F. Tabanus bifarius Loew. Chrysozona crassicornis Wahl. Chrysozona pluvialis (L.) Ochrops rusticus L. Lapharia fulva Mg. Philonicus albiceps Mg. Exoprosopa jacchus F. Exoprosopa germari Wied. Villa hotentota L. Anthrax fenestratus Fall. Bombylius major L. Tachista sabulosa Mg. Syrphus tricinctus Fall. Syrphus torvus O.-S. Syrphus balteatus De Geer. Erystalomyia tenax L. Xylota femorata L. Sapromyza bipunctata Kieff. Cnemodon vitripenis (Meigen) Lonchaea chorea F. Chilosia melanura Beck. Piophila caripes Mg. Calobaea bifasciella Mg. Ctenulus pectoralis Z. Salticella fasciata Mg. Bischoffia simplex Fall. Tetanocera arrogans Mg. Oxytaenia mikiana Hend. Meroplius stercorrarius Rob. Nemopoda nitidula Fall. Themira putris L. Themira anulipes Mg. Limosina limosa Fall. Rhamphomyia marginata L. Melieria omissa Loew. Euconnus watterhali Gyll. Choleva oblonga Mull. Ptomaphagus varicornis Rosh. Scioderpa watsoni Spin. Ephydra macellaria Egger Fucellia maritima Hall. Sepsis thoracica Rob.-Desv. Coremacera catenata Scop. Trypetoptera punctulata Scop. Hemipenthes morio Loew. Catops tristis Panz. Fannia scalaris F. Muscina stabulans Fall. Musca tempestiva Fall. Pyrella cadaverina L. Heteronychia rohdendorfi P.-S. Oxytaenia mikiana Hend. Meroplius stercorarius R.-D. Nemopoda nitidula Fall. Sarcophaga carnaria L. Bercaea hamorrhoidalis Fall. Platystoma seminationis L. Cylindomyia brassicaria F. Tephromyia grisea Mg. Metopia leucocephala Rossi Histochaeta marmorata F. Gymnosoma rotundatum L. Echinomyia prompta Mg. Lucilia ruficeps Mg. 102 Lucilia sericata Mg. Limnophora notata Fall. Dexia rustica F. Spilogona dispar Fall. Lispa hydromysina Fall. Hymenoptera The wasps and bees encountered in the littoral area are fewer compared to the Diptera or Coleoptera (Andriescu, 1993; Constantineanu et Constantineanu, 1993, 1997, 1998; Constantineanu, 1965; Ionescu, 1957, 1973 ; Iuga, 1958 ; Konnerth-Ionescu, 1963; Lacatusu, 1968; Nagy, 1968; Negru, 1965; Pascu, 1996, 1997; Scobiola, 1960, 1963; Scobiola-Palade, 1965, 1968, 1978, 1981). Among these species there are those that hunt on the beach and those that are parasites for larvae or adults of Diptera or Coleoptera. Anthophylous species are rare and only occur accidentally on the inflorescence of plants in the herbaceous vegetation area. Teleas rugosus Kieff. Bombus agrorum L. Teleas lamellatus Kieff. Bombus terrestris L. Brachymeria minuta L. Bombus lapidarius L. Vespa germanica L. Brachymeria intermedia Nees Haltichella rufipes Oliv. Pompilius plumbeus F. Ammophila sabulosa L. Ammophila heydeni Dhlb Ammophila hirsuta Scop. Ammophila affinis Kirby Ammophila morawitzi Andr. Bembix oculata Latr. Bembix olivacea Cyr. Cerceris rybyensis L. Liris nigra Lind. Stizus distinguendus Hand. Philanthus triangulum F. Philanthus coronatus F. Philanthus venustus Rossi Tetramorium caespitum L. Formicoidea Myrmecocystus cursor Fonsc. Myrmecocystus viaticus F. Myrmecocystis varialei Em. Messor structor Latr. Scelionidae Sparasion frontalis Latr. Megachilidae Eriades maxillosus L. Anthidium variegatum F. Lithurgus chrysurus F. Apoidea Dasypoda plumipes Drury Amegilla quadrifasciata quadrifasciata (Villers) Tetralonia ruficornis (Mocsary) Amobates (amobates) punctatus (Fabr.) Xylocopa violacea L. 103 The entomofauna in the Bulgarian littoral The area included in the project, located as far as Cape Kaliakra, is characterized by a much richer habitat diversity, compared to the Romanian littoral area. Thus, if the northern part of the Bulgarian littoral, between Krapets and Durankulak, is characterized by sandy beaches stretched in the vicinity of paramarine lakes or high loess seawalls, south of cape Shabla the seawall becomes rocky and its height rises to over 50 meters. In this case, a new type of habitat occurs – rather a complex of habitats – characterized by a different entomofauna that can be seen north of Vama Veche. Thus, the seawall plateau is often terraced and covered by shrubs and tree clusters in which certain species of southern origin occur. A particular complexity in terms of habitat structure can be encountered in Kamen Bryag, Yailata, Rusalka, Bolata Dere and the south-oriented seawall from cape Kaliakra, where a particular vegetation develops and shelters a largely unstudied entomofauna. Considering these reasons, we appreciate that the entomofauna of the Bulgarian littoral is much richer compared to the one at the Romanian littoral. The dune vegetation areas, exceptionally well preserved both in Durankulak and Shabla, permit the existence of important invertebrate populations that occur only isolate in the Romanian littoral area (the Agigea and Eforie South zones have been strongly affected by the anthropogenic impact and only preserve partially the characteristic species). However, the richest, most interesting and complex entomofauna can be encountered in the portions where the limestone seawall, furrowed by a system of fissures and caves (which permit the development of a characteristic fauna), is terraced and covered by forest, as well as the seawall in cape Kaliakra, where the underground water drains permit the development on the almost vertical wall of a vegetation that is mostly hygrophile, looking like a jungle. Sadly, these areas have not been studied by specialists interested in more detailed entomofauna studies and unfortunately, in some cases (Rusalka), the anthropogenic impact can already be seen. These areas are protected at national level, which means, at least theoretically, that their very important entomofauna biodiversity and flora are preserved. The Durankulak Area. It is characterized by the presence of a littoral strip that separates the lake from the sea, a strip on which vegetal associations characteristic to the marine dunes occur. They are very well preserved due to the inexistence of an access route and to the fact that the anthropogenic impact in the area is minimal compared to the Romanian littoral. In the north and south, the high loess seawalls are covered with herbaceous vegetation, while the ridge of the seawalls display plants of different wood types, from Fraxinus ornus and Carpinus orientalis to Pinus nigra and Amorpha fruticosa. At the basis of the seawall that edges the littoral strip in the north, there are very well preserved associations dominated by Crambe maritima. All these habitats are completed by the presence in the immediate vicinity of Lake Durankulak with wetland vegetal associations. In this area, the invertebrate fauna is much richer compared to the area north of cape Midia, where there are no wetlands even though there are high seawalls. Important populations of Orthoptera have been identified as they are characteristic to the associations dominated by sand plants such as Acrotylus longipes present in extremely large numbers starting with June. A considerable number of Cicindela hybrida also occurs in May. In the area with Crambe maritime, the population of the Mediterranean Heteroptera Eurydema spectabile reaches a very high density, the number of individuals per one plant exceeding 200. Among Lepidoptera – which are quite numerous in the area due to the habitat diversity – are worth mentioning especially Lycaena dispar – characteristic to wet habitats – and Zerynthia hypsipyle, both being on the lists of the Habitat Directive. The forest skirts south and north of the littoral strip shelter a considerable number of species of lepidopters such as Euchloe ausonia, Brenthis daphne, Argynnis pandora, Melitatea phoebe, Melanargia galathea, Zygaena filipendulae while the flowers in the littoral strip Astragallus attract a large number of Colias croceus, Vanessa cardiu, Aricia agestis, Polyommatus icarus, Polyommatus bellargus. A number of rare species are cited in the area such as Scopula corrivalaria and Diachrysia chryson deltaica signaled in Bulgaria only in this area, as well as Triodia amasinus dobrogensis, Macrochilo cribrumalis, Schrankia costaestrigalis, Eupithecia variostrigata, Eupithecia inturbata, Diachrysia 104 nadeja, Athetis furvula, Proxenus lepigone, Apamea sicula, Agrotis obesa scitha, Agrotis vestigialis, Pelosia obtusa, Hyles hippophaes, Colias erate, Pseudophilotes vicrama, Melitaea trivia (Abadjiev, Beshkov, 2007). The Shabla Area. The marine dunes in this area are larger compared to those in Durankulak, but they shelter a smaller entomofauna due to th fact that the vegetation is also poorer in species. Common species have been identified in this area: Pieris rapae, Colias croceus, Lycaena phlaeas, Polyommatus icarus, Coenonympha pamphilus alongside the noctuid Drasteria caucasica, species characterisitc to the sandy habitats. Other species are cited in the specialized literature in the area of sand dunes and neighboring wetlands, such as Triodia amasinus dobrogensis, Eupithecia variostrigata, Eupithecia biornata, Eupithecia ochridata, Oxicesta geographica, Simyra albovenosa, Schrankia costaestrigalis, Cucullia asteris, Proxenus lepigone, Archanara dissoluta, Agrotis vestigialis, Pelosia obtusa, Rhyparioides metelkana, many of them present in Durankulak, an area similar in many aspects regarding the habitat conditions (Abadjiev et al, 1999; Abadjiev, Beshkov, 2007; Beshkov, Abadjiev, 2000) Cape Kaliakra – Bolata Dere Located at the southern extremity of the littoral area north of cape Kaliakra, Bolata Dere valley represents an extremely interesting mixture of habitats. Thus, the narrow valley oriented east-west is sheltered by strong winds, except those that blow from the sea. The valley is swampy, populated by associations of hygrophile plants and associations of xerophile bushes on the slopes dominated by species such as Paliurus spina-christi. The valley and sea plateau are dominated by Iris and Asphodeline lutea. In this sheltered valley, the diurnal Lepidoptera are represented by common species Papilio machaon, Iphiclides podalirius, Anthocaris cardamines, Gonepteryx rhamni, Lycaena phlaeas – as well as by rarer species such as Pyrgus sidae sau Melitaea trivia. The cape Kaliakra area is very interesting in what regards the invertebrate fauna. The high seawall (over 50 m), south oriented, offers shelter from the dominant winds and permits the development of an extremely interesting vegetation with numerous species characteristic to wetlands (due to the numerous water infiltrations) and thermophile species that form associations with jungle aspect. On the limestone plateau, there is a xeric habitat characterized by species adapted to a very dry climate. Among them, the enormous agglomerations of xerophile Gasteropoda, as well as large populations of Orthoptera that populate the plateaus with natural vegetation above the seawall. A number of interesting Lepidoptera have been indentified during the field trips, such as Strymon ilicis, Zygaena ephialtes, alongside common species such as Argynnis pandora, Pararge megera or Synaphe moldavica. The Lepidoptera fauna in cape Kaliakra also includes rare species, such as Lycaena dispar, Maculinea arion, Catopta thrips – present on the lists of the Bern Convention, a number of subspecies characterized by the light colors of their wings (feature directly connected to the limestone soil) – Autophola asiatica argentea, Autophila dilucida argentea, Auchmis detersa argentea, Caradrina pertinax argentea, Dichagyris melanura albida, Dichagyris renigera argentina, Dichagyris flavina pretiosa, Agrotis obesa nivea, Meganola albula nivalis. These are completed by rare and localized species such as Triodia amasinus dobrogensis, Oncocnemis michaelorum, Lemonia balcanica, Lasiocampa quercus, Nychiodes waltheri, Eupithecia variostrigata, Pandesma robusta, Clytie syriaca, Panchrysia aurea, Oxicesta geographica, Cryphia ochsi, Cryphia amasina, Acontia titania, Pyrrhia purpurina, Pyrrhia victorina, Eutelia adoratrix, Mycteroplus puniceago, Proxenus lepigone, Chortodes morrisii, Oxytripia orbiculosa noctivolans,Lacanobia praedita, Hadula odontites, Hadena persimilis, Euxoa cos crimaea, Euxoa conspicua, Nola cristatula, Nycteola siculana, Sphingonaepiopsis gorgoniades, Hyles gallii, Hyles hippophaes, Thymelicus acteon, Pyrgus cinarae, Pseudophilotes vicrama, Glaucopsyche alexis, Plebejus sephirus, Melitaea trivia, Melitaea aurelia, (Abadjiev, Beshkov, 2007). Apart from the Lepidoptera, it is worth mentioning the presence in the area of an Orthoptera – Asiotmethis limbatus – species characteristic to the limestone habitats, rare and localized in eastern Europe, present also in the Romanian Dobrogea and once signaled in the Romanian littoral area, but currently extinct. 105 Rusalka. The Rusalka area is quite similar as habitat structure with cape Kaliakra. The difference lies in the fact that the limestone plateau is crashed forming a series of 4-5 successive terraces, covered by a complex of trees and shrubs that alternate with clearings dominated by herbaceous plants. The limestone plateau is dominated by herbaceous plants, but the habitats are less dry compared to the high seawall in Kaliakra. In this area, the entomofauna is extremely interesting, comprising on a reduced territory, species characteristic to the marine beaches, to the limestone seawalls, to the east-Balkan thermophile forests or to the steppe habitats. Among Lepidoptera, we remark the presence of interesting species that have not been observed in the other areas investigated during the Program PHARE CBC RO2005/017-535.01.02.02. Thus, among the rhopalocera, the following species were observed in July Strymon accaciae, Scolitantides orion and Pseudophilotes vicrama, Philotes baton (present also in Bolata Dere and cape Kaliakra), Pyrgus cirsii, Pyrgus armoricanus. Conclusions Analyzing comparatively the two areas studied from a biodiversity point of view within the Project PHARE CBC RO2005/017-535.01.02.02 the conclusion is that there are a number of similarities and differences between the Romanian littoral area and the Bulgarian one. Thus, the Romanian littoral displays (from a biodiversity point of view as well) a continuation north of the limestone shore in the Cape Kaliakra area. The diversity of the entomofauna decreases from south to north with the disappearance of certain habitats – limestone seawalls covered with tree clusters – north of cape Shabla. From the point of view of the entomofauna, three types of associations can be distinguished in this area of the western littoral of the Black Sea: a dominant association of forest and steppe species south of cape Shabla, an association with steppe and maritime dunes species between cape Shabla and cape Midia and a dominant association with species characteristic strictly to the littoral strips – north of cape Midia. From far, the richest in number of species is the area between Yailata and cape Kaliakra. From the point of view of the originality of fauna associations in the Romanian littoral area, the wild beaches area can be distinguished on the one hand, where human influence is minimal and where numerous populations of insects still remain alongside other invertebrates that feed either on vegetal or animal remains thrown by waves onto the beach, or on the vegetation characteristic to the sandy beaches. These areas suffered the most in the past because of the anthropogenic impact and we appreciate that they should be protected everywhere where it is necessary. Unfortunately, the entomofauna of these areas is mostly not studied, either at the level of taxonomy or ecology. Studies to outline the complex relationships among different species of insects in the vegetal associations in the littoral area should be a priority in order to understand the structurs of these habitats characteristic to the Pontic region. Due to the fact that a large part of the wild littoral is included in the Danube Delta Biosphere Reservation, the unaltered preservation of these habitats can be considered certain today. The Agigea Maritime Dunes Reservation and the seawalls in the southern littoral do not share a similar situation. Firstly, the reduction of reservation surface and the severance of any direct connection to the seashore (the harbor installations Constanta South-Agigea are currently located in front of the reservation) have led to the turning of the reservation into steppe which made the once sands lie almost entirely fallow, except a very small surface in the north. This way, the initial flora and fauna have changed profoundly. Still, that surface is protected by law, which means its protection is certain. The seawalls in the southern littoral are an interesting area where the flora and fauna characteristic to the original steppe interpenetrates the beach flora and fauna. If in the close past this area was extremely little affected by human activities, the accelerated rhythm of construction in some parts of the southern littoral in the superior part of the seawall raises a number of problems now. Due to the sewage system which is located in the close vicinity of the seawalls, the soil quality will inevitably change as certain opportunistic plant species will enter and thus deeply alter the original flora. This kind of situations occurred over the entire length of the seawall 106 in the vicinity of the cities and towns of Constanta, Eforie North or Eforie South, where the flora is currently dominated by weeds. This is why we consider imperative the decision to declare protected areas these seawall zones currently unaffected by the anthropogenic impact. In the Bulgarian littoral, the degree of preservation is much higher. The lack of access routes, of large urban agglomerations in the littoral area and the lack of harbors and resorts make the area between Durankulak and cape Kaliakra much better preserved, compared to the Romanian littoral. A large part of the coastline is included in different protected areas, which is a guarantee for its protection in the future. However, a widening of these areas is desired in order to create a green corridor. This would also prevent the development of any considerable projects that would alter the habitats radically. A general conclusion regarding the fauna of invertebrates in the analyzed area is that the correct way is to treat this area as a continuum from this point of view as well, the gradual modification of the fauna being in fact a reflection of the habitat structure in the coastal area. References 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. ALBU PAULA, 1980 Fam.Chironomidae, subfam.Chironominae in Fauna Rom.Vol.XI, fasc 13, Ed.Acad. ANDRIESCU I., 1993 – Contributii la studiul calcidoidelor (Insecta, Hymenoptera, Chalcidoidea) din Rezervatia Biosferei I Conspectul faunistic.An.St.Inst.Cerc.Vol.II: 49-58. ABADJIEV S., BESHKOV S., 2007 - Prime butterfly areas in Bulgaria, Pensoft Series Faunistica 69, 227 pp. ABADJIEV S.P., TSHIKOLOVETS V.V., BESHKOV S.V., 1999 - Notes on some late summer butterflies of Bulgaria with a short zoogeographical analysis (Lepidoptera: Hesperioidea & Papilionoidea).Atalanta 30 (1/4): 273- 276. BESHKOV S.V., ABADJIEV S.P., 2000 - The butterfly and moth fauna of the areas around the lakes of Durankulak, Ezerets, Shabla and Shablenska Tuzla in NE Bulgaria (Insecta: Lepidoptera). Atalanta 31 (3/4): 543-573. BOGOESCU C., 1958 – Ephemeroptera, in Fauna Romaniei, Vol.VIII, 3, Ed.Academiei Bucuresti BULIMAR FELICIA, 1992 – Compozitia faunistica si structura comunitatile de colembole (Collembola: Insecta) in ecosistemele stuficole din An.St.Inst.Cerc. Vol.I: 95-100 BULIMAR FELICIA, 1993 – Studiul faunei de odonate din Delta Dunarii si zonele invecinate, An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.II: 87-92. CÂRDEI F., BULIMAR FELICIA, 1963 - Odonata in “Fauna R.P.R.”, Insecta, vol.VII, fasc.5, Edit.Acad.Rom. CEIANU I., 1999 - Contribution to the knowledge of shore flies (Diptera: Ephydridae) in Romania, Entomol.Rom.3: 125-136. CIUBUC C., 1993 – Checklist of Romania Trichoptera (Insecta), in Travaux Mus.Hist.Nat.“Gr.Antipa”, XXX III, 11-147. CONSTANTINEANU M., 1965 – Hymenoptera Ichneumonidae (sf.Phaeogeninae, Alomyinae), Fauna Rom.IX, 5 CONSTANTINEANU R., CONSTANTINEANU IRINEL, 1993 – Contributii la cunoasterea ihneumonidelor (Hymenoptera, Ichneumonidae) din Delta Dunarii si imprejurimi (I), An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.II: 171-176. CONSTANTINEANU R., CONSTANTINEANU IRINEL, 1994 – Contributii la cunoasterea ihneumonidelor (Hymenoptera, Ichneumonidae) din Delta Dunarii si imprejurimi (Nota II), An.St.Inst.Cerc. Delta Dunarii, Tulcea,Vol.III (1): 129-134. CONSTANTINEANU R., CONSTANTINEANU IRINEL, 1997 – Contributions to the knowledge of Ichneumonidae from Macin Mountains; Entomol.Rom.2: 102-114 107 16. CONSTANTINEANU IRINEL, CONSTANTINEANU R., 1998 – Contributions to the faunistic and ecological study of Ichneumonids (Hymenoptera – Ichneumonidae) in the Danube Delta Biosphere Reservation.Memoriile Sec .Stiint ifice, Acad.Rom.Seria IV, tom XXI, 145-188 17. CRISAN AL., 1993 – Date asupra familiei Chrysomelidae (Coleoptera) in partea sudica a Deltei Dunarii, An.St.Inst.Cerc. Vol.II: 67-74. 18. CRISAN Al., 1994 – Noi date asupra familiei Chrysomelidae (Coleoptera) in Rezervatia Biosferei Delta Dunarii, An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.III: 159-166. 19. DINULESCU GH., 1958 – Diptera Tabanidae, “Fauna RPR”, Insecta, Vol.XI, fasc, 2.Edit.Acad.Române. 20. FUHN I., GHERASIM V., 1995 – Arachnida – Salticidae, Fauna Romaniei, Vol.V, 5, Ed.Academiei, Bucuresti 21. FUHN I., NICULESCU-BURLACU FLORIANA, 1971 – Arachnida – Lycosidae, Fauna Romaniei, Vol.V, 3, Ed.Academiei Bucuresti 22. GRIEBLER C., 1994 – Investigations on the fauna of dragonflies in the Danube Delta, An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.III: 113-120. 23. GROSSU A.V., 1983 – Gastropoda Romaniae, Ord.Styllomatophora, Ed.Litera, Bucuresti. 24. GROSSU A.V.., 1987 - Gastropoda Romaniae, Vol.2, Ed.Litera, Bucuresti. 25. GROSSU A.V., 1993 – The catalogue of the molluscs from Romania, Travaux Mus.Hist.Nat.“Gr.Antipa”, XXX III, 291-366. 26. IENIŞTEA M., 1968 – Die Hydraeniden Rumaniens (Coleoptera, Hydraenidae), in Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.VIII (2): 759-795. 27. IONESCU M.A.1957 – Hymenoptera-Cynipinae, Fauna Rom.IX, 2 28. IONESCU M.A., 1973 – Biologia Galelor, Ed.Acad, Bucuresti. 29. IONESCU M., WEINBERG MEDEEA, 1960 – Contribution a l’etude des dipteres asilides de la RPR – I, in Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol, II: 213-227. 30. IONESCU M., WEINBERG MEDEEA, 1963 – Some dipterous insects (Fam.Asilidae) from the collection of the Bruckenthal Museum – Sibiu, in Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol, IV: 290-314. 31. IONESCU M.A., WEINBERG MEDEEA, 1971 Diptera-Asilidae, Fauna Rom.XI/11 32. IUGA VICTORIA, 1958 – Hymenoptera - Apoidea, “Fauna R.P.R”, Insecta, Vol.IX, fasc.3, Edit.Acad.Române 33. KIS B., 1985 – Heteroptera, in Fauna Romaniei, Vol.VIII, 8, Ed.Academiei, Bucuresti 34. KIS B., 1993 – Originea faunei de ortoptere din Rezervatia Biosferei Delta Dunarii, An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.II: 63-66. 35. KIS B., NAGLER C., MANDRU C., 1970 – Neuroptera, in Fauna Romaniei, Vol.VIII, 6, Ed.Academiei, Bucuresti 36. KNECHTEL W., 1951 – Thysanoptera, in Fauna Romaniei, Vol.VIII, 1, Ed.Academiei, Bucuresti 37. KNECHTEL W., POPOVICI-BAZNOSANU A., 1950 – Orthoptera, in Fauna Romaniei, Vol VIII, 4, Ed.Academiei, Bucuresti 38. KONNERTH-IONESCU ANNELISE, 1963 – Halticinae recorded from Romania till 1961, in Trav.Mus.Hist.Nat.“Gr.Antipa” Vol.IV: 251-267. 39. KOVACS Z., KOVACS S., 1998a – Familia Eriocranioidae (Lepidoptera) in Romania, Bul.Inf.Soc.Lepid.Rom.9(1-2): 9-27 40. KOVACS Z., KOVACS S., 1998b – Familia Micropterigidae (Lepidoptera) in Romania, Bul.Inf.Soc.Lepid.Rom.9(1-2): 29-44 41. KOVACS Z., KOVACS S, 1999a – Familia Adelidae (Lepidoptera) in Romania, Bul.Inf.Soc.Lepid.Rom.10(1-4): 9-66 42. KOVACS Z., KOVACS S, 1999 b– The commented checklist of Gelechiidae (Lepidoptera) of Romania, Entomol.Rom.4:11-44 108 43. LACATUSU MATILDA, 1968 – Nouvelles donnees sur les braconides (Hymenoptera) de Dobroudja, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.VIII (2): 827-840. 44. MATIC Z., 1966 – Chilopoda – Anamorpha, in Fauna Romaniei, Vol.VI, 1, Ed.Academiei, Bucuresti 45. MATIC Z., 1992 – Chilopodele din Delta Dunarii, An.St.Inst.Cerc.Delta Dunarii Tulcea, Vol.I.: 9394 46. NAGLER C., 1968 – Les panorpides de la collection du Mesee “Grigore Antipa” – Bucarest, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.VIII (2): 813-826. 47. NAGY C., 1968 – Quelques especes nouvelles d’hymenopteres heterogynes en Roumania, Trav.Mus.Hist.Nat."Gr.Antipa”, Vol.VIII (2): 1029-1035. 48. NAGY C., 1971 – Beobachtungen uber die rolle der Insekten des Supralittoral in Rumanischen kustenbereich des Schwarzen Meeres, Cerc.Marine IRCM, 2: 27-36 49. NAGY C., 1972 – Contribution a l’etude des insectes du supralittoral du secteur roumain de la Mer Noire, Cerc.Marine IRCM, 3: 171-189 50. NEACSU P., 1965 – Nouvelles contributions a la connaissance des Dipteres – Itonididae, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.V (2): 899-907. 51. NEGREA ALEXANDRINA, 1994a - Contributii la cunoasterea gasteropodelor din Dobrogea (Romania), St.Cerc.Biol., Biol.Anim, Tom 46/1 : 3 – 15. 52. NEGREA ALEXANDRINA,, 1994b – Gasteropodes (Gastropoda) connus jusqu’a present des provinces biospeologiques de Roumanie, Trav.Mus.Hist.Nat.“Gr.Antipa”, XXXIV: 227-264. 53. NEGRU ST., 1965 – Les guepes-dorees (Hymenoptera, Chrysididae) de la Collection scientifique du Museum “Gr.Antipa” Bucarest, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.V: 191-207. 54. NEGRU ST., 1994 – Chilopodes (Chilopoda) cavernicoles de Roumanies connus jusqu’a present, Trav.Mus.Hist.Nat.“Gr.Antipa”, XXXIV: 265-283. 55. NITU E., 1992 – Specii de carabide noi pentru fauna Dobrogei si a Deltei Dunarii; An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.I: 119-120. 56. OLTEAN CLEOPATRA, 1968 – Contributions a l’etude des araignees de Dobroudja (foret de Babadag), Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.VIII (2): 691-698. 57. OSTAFCIUC V., 1994 – Fauna stafilinidelore (Coeloptera – Staphilinidae) si elateridelor (Coleoptera – Elateridae) rezervatiei biosferei Delta Dunarii .An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.III: 85-86. 58. PARVU C., 1993a – Genus Haematopogon Meigen (Diptera, Tabanidae) in Romania.A study on female genitalia, variability and distribution of the species, in Travaux du Mus.Hist.Nat.“Gr.Antipa”, XXXIII: 165-199 59. PARVU C., 1993b – The Tabanid species (Diptera, Tabanidae) of Romania, rpeserved in the scientiffic collections of “Grigore Antipa” Natural History Museum of Bucharest, in Travaux du Mus.Hist.Nat.“Gr.Antipa”, XXXIII: 201-214, 215-227. 60. PARVU C., 1993c – A critical analysis of Tabanid species (Diptera, Tabanidae) mentioned in Romania, in Travaux du Mus.Hist.Nat.“Gr.Antipa”, XXXIII: 215-227. 61. PASCU MARIANA, 1996 – Catalogul Suprafamiliei Apoidea (Hymenoptera) din colectiile Muzeului de Istorie Naturala Sibiu - I, Bul.Inf.Soc.Lepid.Rom.7(3-4): 283-296 62. PASCU MARIANA,, 1997 – Catalogul Suprafamiliei Apoidea (Hymenoptera) din colectiile Muzeului de Istorie Naturala Sibiu - II, Bul.Inf.Soc.Lepid.Rom.8(3-4): 261-273 63. POPOVICI LIVIA-RODICA, 1992 – Varietatea specifica a carabidelor din Delta Dunarii, An.St.Inst.Cerc.Delta Dunarii Tulcea, Vol.I: 111-118. 64. RAKOSY L., 1997 – Die endemischen Lepidopteren Rumaniens, Entomol.Rom.2: 59-81. 65. RAKOSY L., SZEKELY L., 1996 – Macrolepidopterele din sudul Dobrogei.Entomol.Rom.1: 17-62, Cluj Napoca 66. RUIC NESCU A., 1995 – Contributii la studiul faunistic si ecologic al buprestoidelor din Rez.Biosferei (Coleoptera: Buprestoidea), Bul.Inf.Soc.Lep.Rom.6(1-2): 105-125 109 67. RUŞTI D., 1992 – Starea actuala a faunei de lepidoptere din Delta Dunarii (Lepidoptera: Rhopalocera, Sphynges & Bombyces), An.St.Inst.Cerc.Delta Dunarii, Tulcea, Vol.I: 121-136. 68. RUŞTI D., 1994 – Additional data to the checklist of Romanian lepidoptera (Insecta: Lepidoptera), Trav.Mus.Hist.Nat.“Gr.Antipa”, XXXIV: 81-93. 69. SCHNEIDER E., PLATTNER H., 1968 – Beitrage zur kenntnis der Coriziden Rumaniens (Heteroptera, Corizidae Dgl.et Sc., Rhopalidae A.et S.), Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.VIII (2): 749-757. 70. SCOBIOLA XENIA, 1960 – Les especes de Sphex Linne et Ammophila Kirby (Hymenoptera, Sphecidae) dans la faune de la Republique Populaire Roumaine, in Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.II: 229-244. 71. SCOBIOLA XENIA, 1963 – Sur quelques pompilodes, nouveaux ou rares de la R.P.Roumanie, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.IV: 269-281. 72. SCOBIOLA-PALADE XENIA, 1965 – Conrtibution a la conaissance des sphecides (Sphecidae, Hymenoptera) de Roumania, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.V: 107-113. 73. SCOBIOLA-PALADE XENIA, 1968 – Nouvelles donnees sur les hymenopteres de la Roumanie, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.VIII (2): 821-826. 74. SCOBIOLA-PALADE XENIA, 1978 – Hymenoptera-Symphyta, Fauna Rom.IX, 8 75. SCOBIOLA-PALADE XENIA, 1981 – Hymenoptera-Symphyta, Fauna Rom.IX, 9 76. SERAFIM RODICA, 1993a – Contribution a la connaissance des Coleopteres Cerambycides (Coleoptera, Cerambycidae) du Delta du Danube et du Complex lagunaire Razelm (Roumanie), in Travaux Mus.Hist.Nat.“Gr.Antipa”, XXX III, 235-246. 77. SERAFIM RODICA, 1993b – La liste des especes de Coleopteres Coccinellides (Coleoptera, Coccinellidae) du du Danube et du Complex lagunaire Razelm (Roumanie), in Travaux Mus.Hist.Nat.“Gr.Antipa”, XXX III, 247-255. 78. SERAFIM RODICA, 1994 – Donnees sur la tribu Scymnini (Coleoptera: Coccinellidae) en Roumanie, Trav.Mus.Hist.Nat.“Gr.Antipa”, Vol.XXXIV: 95-115. 79. SERAFIM RODICA, RUICANESCU A., 1995 – Lista speciilor de Buprestoidea (Coleoptera) din colectia N.Savulescu a Muzeului de Istorie Naturala “Gr.Antipa” din Bucuresti.Bul.Inf.Soc.Lep.Rom.6(1-2): 123-144 80. SKOLKA M., 1994 – Date referitoare la lepidopterele din Dobrogea (Grypocera – Rhopalocera), Bul.Inf.Soc.Lepid.Rom, 5 (3-4): 223-244. 81. TEODOR L., 1993 – Contrinutii la cunoasterea curculionidelor (Coleoptera) din Delta Dunarii. An.St.Inst.Cerc.Delta Dunarii Tulcea, Vol.II: 193-196. 82. TEODOR L., TRAIAN M., 1996 – Noi contributii la cunoasterea curculionidelor din Rezervatia Biosferei “Delta Dunarii ” (Coleoptera: Curculionidae), Bul.Inf.Soc.Lep.Rom.7(3-4): 261-269 83. VASILIU-OROMULU LILIANA, 1992 – Studiul ecologic si zoogeografic al faunei de tisanoptere (Ord.Thysanoptera) din Delta Dunarii, An.St.Inst.Cerc.Delta Dunarii Tulcea, Vol.I: 101-106. 84. VASILIU-OROMULU LILIANA, 1998 – Endemits, relicts and vicariant Thysanoptera species from Romania (Insecta: Thysanoptera), Entomol.Rom.3: 59-62. 85. VICOL V., 1997 – Lista suplimentara de semnalari a microlepidopterelor din Romania.Bul.Inf.Soc.Lepid.Rom.8(3-4): 189-198. 86. WEINBERG MEDEEA, 1994 – Data on the family Micropezidae (Diptera) and its occurrence in Romania, Trav.Mus.Hist.Nat.“Gr.Antipa”, XXXIV: 125-131. 110 STUDY ON THE AVIFAUNISTICAL DIVERSITY IN THE COASTAL AREA BETWEEN CAPE MIDIA (ROMANIA) AND CAPE KALIAKRA (BULGARIA) Gabriel BANIC Universitatea Ovidius Constanta, Facultatea de Stiinte ale Naturii si Stiinte Agricole, Mamaia Bd., No. 124, 900527, Constanta, Romania, gabibiosys@yahoo.com __________________________________________________________________________________________ Abstract: The paper presents the result of the ornithological observations made in the summer of the 2008 on the wetlands from the Romanian and Bulgarian Black Sea coast. We observed 172 species of birds: in Romania 153 species and in Bulgaria 121 species. Some of this species we have seen only on the Romanian sea coast, some of them only on the Bulgarian sea coast. There are significant differences between the habitats from the two countries and the anthropic impact. They are still important bird populations in this area, but the human impact has a very big influence on these populations. We need solutions for the protections of this beautiful area. Keywords: Birds, Black Sea Coast, Wetlands, Bulgaria, Romania. __________________________________________________________________________________________ Introduction Habitats. Birds are dependent on the habitats they are living in, just as any other living creature. Naturaly, this means that habitat variety will lead to an even larger bird species diversity. The coastal habitats between Cape Midia and Cape Kaliakra are varied and alternate some with others. This favors bird populations, offering them great living conditions. Unfortunately, the coastal area is more and more under anthropic influence. People have a great tendency towards the coastline, proven by the large number of settlements (cities and holiday resorts) present everywhere on the globe. There is an important traffic, both terrestrial and aquatic. The warm season is reserved to aestival tourism, a factor extremely disturbing for the birds which may nest here. We believe that habitat variety, alongside the anthropic impact are the leading factors in determining the area’s bird diversity. In the studied area, we can distinguish the following types of the habitat: • • • The Black Sea. This is about the sea’s water surface situated close to the shore. Here, species of waterfowl and good flying birds can find shelter, birds belonging to Gaviiformes, Podicipediformes, Anseriformes, Charadriiformes orders and Fulica atra. Of course, this is not only a nesting place, it is just an area destined to resting and feeding. Marine Beach. There exists an entire series of beaches in the studied area, fine feeding and resting place for Charadriiformes species (limicoles, gulls and terns). These should’ve also been fine nesting places of this species, but because of the tourists and other anthropic activities, practically, these beaches cannot be used this way. Claysh cliffs. These cliffs are found especially in the Romanian area, as the cliff between Tuzla and Costinesti or the cliff between 2 Mai and Vama Veche. A similar cliff is found at Durankulak, in the north (Bulgaria). These are less affected areas by the human influence, and can still provide fine nesting places for species which build their nests here, as the Falco tinnunculus, Coracias garrulus, Merops apiaster, Sturnus vulgaris, Passer montanus. 111 • • • • • Stony cliffs. This sort of cliff does not exist in Romania, only in Bulgaria, at Kamen Bryag, Yaylata, Rusalka and Kalyakra Cape. These are tall cliffs, which are of little use to men. For this reason, they are favourable for the nesting places of some birds as the Oenanthe pleshanka, largely spread in the area. Coastal steppes. If in Romania this habitat almost does not exist anymore (in the coastal area), because of the antropic aggression, in Bulgaria, steppes still can be found above cliffs, at Kamen Bryag, Yaylata, Rusalka and Kaliakra Cape. Here nest birds characteristical of open areas, as the Burhinus oedicnemus, Melanocorypha calandra, Alauda arvensis, Lanius collurio, Lanius minor, Anthus campestris, Motacilla alba, Passer montanus, etc. Litoral lakes. More or less influenced by human activity, the lakes are excellent habitats, for a large number of bird species. Practically, several ecosystems can be found here, from the beaches, reed beds, open water surfaces or bushes of the shore, good places for birds, good for nesting and also for resting or feeding. There are many lakes situated in the near vicinity of the sea-side, both in Romania (especially) and Bulgaria. A large number of aquatic species may be found here. Forested areas. Forests do not exists in the word’s true meaning in the studied area, but there are some areas with trees and bushes, there are parks, which are good habitats for a large number of birds (Passeriformes). Usually, these are not good nesting places, but during migration and in the cold season, they are great refugees for many species of birds. Anthropic habitat. Here species of birds are found characteristical to settlements and harbours. The birds here have an importance which is not to be neglected, especially now that some species have started conquering this new territory, as the Larus cachinnans, bird nesting in the cities on the Romanian sea-coast. Here, is an extremely brief, a presentation of the principal habitats in Dobruja’s coastal area. Of course, wet areas are prioritary and have the utmost importance for local birds. Migration. The coastal area in the west of the Black Sea is one of the most important way of migration in Europe. Here, the Pontic and Sarmatic ways are found, followed by a large variety of species. This means that during spring and fall, both the Bulgarian and the Romanian coasts are passed by a large number of birds, especially aquatic birds, but also small passerines (Passeriformes) and birds of prey (Falconiformes). Most species of migrating birds in the Danube Delta follow this route. Birds that nest in northern Europe and even in northern Asia fly, in the majority of cases, along the west coast of the Black Sea. This fact makes bird fauna in the coastal area of Bulgaria and Romania become distinctly rich (leading to a large avifaunistical diversity). For this reason, the existence of resting and feeding places for birds is extremely important for their survival. We mention only the wetlands of Techirghiol Lake and Hergheliei Swamp, from Romania (Banica, G. 1996, Banica, G. 2000) and Durankulak Lake and Sabla Lake (Bulgaria). Wintering. There exist many aquatic species that winter in the wetlands on the shores of Dobruja (both Romanian and Bularian). This fact increases the specific diversity of birds from the area. For the the red breasted goose (Branta ruficollis), Dobruja it’s the main wintering area. To illustrate the distinct importance of this area for aquatic birds wintering here, we need to mention that the numbers of the species from the Orders Gaviiformes, Podicipediformes, Pelecaniformes, Ciconiiformes, Anseriformes, Gruiformes si Charadriiformes of this period of the year can go beyond one million individuals (Munteanu, D. et al. 1989). Antropic impact. Since the dawn of time, people have preferred the closeness of water. This is why the sea side has always been a favourite place for settling. Unfortunately, the large urban crowding on the sea shores contributed decisively to chasing birds away from these areas. Some birds from the sea coast have witnessed their habitat become more and more restrained. Here are some differences between the Bulgarian and the Romanian coast. While the Romanian shore is invaded and even suffocated with construction (between Cape 112 Midia and Vama Veche), between Durankulak and Cape Kaliakra, the sea shore is far less affected by anthropic activities. This fact makes us hope that at least this area will be protected in the future for the benefit of bird populations transiting the area year after year. The anthropic impact on the Romanian sea side will lead to less bird species nesting here, because during the warm season come the most important waves of tourists, which greatly inconvenience the area. On the other hand, during winter and spring, most touristical locations remain unhabited, and birds, especially the aquatic species, can find great resting and feeding places. In wetlands from Bulgarian coastal areas, some birds can still nest under fine conditions, an example being the nesting colony of cormorants (Phalacrocorax carbo sinensis) from Durankulak. In Romania, litoral lakes are used as fish farms (with one exception, Hergheliei Swamp). The exploitation of fish resources leads to a conflict between fishermen and fisheating birds. The disturbance provoked by the farm staff can influence other species of birds. During summertime, lakes are also used by tourists, fact contributes to the disturbance of birds. Material and Methods We used binoculars (usually Olympus 10x50) and telescopes (usually Optolyth 30x75) for our observations. We made transects along the sea coast and along the lakes side, in order to identify the species of birds and their numbers (effectivs). The book-guides used are Bruun, B. et all. 1999, Peterson, R. et all. 1989 and Svensson, L. et all. 2000. Our observations from Bulgaria were made in: 09.05.2008–11.05.2008, 06.06.2008–08.06.2008, 18.07.2008-20.07.2008 and 08.08.2008-10.08.2008. The points of observations in Bulgaria were Durankulak (the sea and the lake), Krapets (on the sea), Shablenska Tuzla (the lake and the sea), Kamen Bryag (the steppe and the sea), Yaylata (the cliff and the sea), Rusalka (the steppe, the cliff, the sea), Bolata Dere (the gorges and the sea), Kaliakra Cape (the steppe, the cliff and the sea) and Kavarna (the sea). The observations from Romania was made in the following Points: Grind Chituc, Vadu, Corbu, Navodari, Mamaia, Constanta, Eforie Nord, Eforie Sud, Costinesti , Mangalia and Vama Veche. Here, the observations were made from April till September. Results and Discussion During our research on the sea side of both countries, the following species of birds have been seen (Table 1 and Table 2 – the names of the birds are according with Munteanu, D. 1998): Table 1 - Bird Species from the North Eastern Bulgarian Black Sea Coast (2008) No. Scientific Name English Name Romanian Name 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Gavia arctica (Linnaeus) Podiceps cristatus (Linnaeus) Phalacrocorax carbo sinensis (Linnaeus) Phalacrocorax aristotelis (Linnaeus) Phalacrocorax pygmaeus (Pallas) Botaurus stellaris (Linnaeus) Ixobrychus minutus (Linnaeus) Nycticorax nycticorax (Linnaeus) Ardeola ralloides (Scopoli) Egretta garzetta (Linnaeus) Casmerodius albus (Linnaeus) Ardea cinerea Linnaeus Ardea purpurea Linnaeus Ciconia nigra (Linnaeus) Ciconia ciconia (Linnaeus) Black-throated Diver Great Crested Grebe Cormorant Shag Pygmy Cormorant Bittern Little Bittern Night-Heron Squacco Heron Little Egret Great White Egret Grey Heron Purple Heron Black Stork White Stork Cufundar polar Corcodel mare Cormoran mare Cormoran motat Cormortan mic Buhai de balta Starc pitic Starc de noapte Starc galben Egreta mica Egreta mare Starc cenusiu Starc rosu Barza neagra Barza alba 113 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 Platalea leucorodia Linnaeus Cygnus olor (Gmelin) Tadorna tadorna (Linnaeus) Anas strepera Linnaeus Anas platyrhynchos Linnaeus Anas querquedula Linnaeus Anas clypeata Linnaeus Aythya nyroca (Guldenstadt) Circus aeruginosus (Linnaeus) Accipiter nisus (Linnaeus) Buteo buteo (Linnaeus) Buteo rufinus (Cretzschmar) Falco tinnunculus Linnaeus Falco vespertinus Linnaeus Falco subbuteo Linnaeus Coturnix coturnix (Linnaeus) Phasianus colchicus Linnaeus Gallinula chloropus (Linnaeus) Fulica atra Linnaeus Haematopus ostralegus Linnaeus Himantopus himantopus (Linnaeus) Recurvirostra avosetta Linnaeus Burhinus oedicnemus (Linnaeus) Glareola pratincola (Linnaeus) Charadrius dubius Scopoli Pluvialis squatarola (Linnaeus) Vanellus vanellus (Linnaeus) Calidris ferruginea (Pontoppidan) Calidris alpina (Linnaeus) Tringa erythropus (Pallas) Tringa totanus (Linnaeus) Tringa ochropus Linnaeus Tringa glareola Linnaeus Larus melanocephalus Temminck Larus minutus Pallas Larus ridibundus Linnaeus Larus genei Breme Larus cachinnans Pallas Gelochelidon nilotica (Gmelin) Sterna sandvicensis Latham Sterna hirundo Linnaeus Chlidonias hybridus (Palllas) Chlidonias niger (Linnaeus) Chlidonias leucopterus (Temminck) 60 61 Bubo bubo (Linnaeus) Streptopelia decaocto (Frivaldszky) Spoonbill Mute Swan Shelduck Gadwall Mallard Garganey Shoveler Ferruginous Duck Marsh Harrier Sparrowhawk Common Buzzard Long-legged Buzzard Kestrel Red-footed Falcon Hobby Quail Pheasant Moorhen Coot Oystercatcher Black-winged Stilt Avocet Stone Curlew Collared Pratincole Little Ringed Plover Grey Plover Lapwing Curlew Sandpiper Dunlin Spotted Redshank Redshank Green Sandpiper Wood Sandpiper Mediterranean Gull Little Gull Black-headed Gull Slender-billed Gull Yellow-legged Gull Gull-billed Tern Sandwich Tern Common Tern Whiskered Tern Black Tern White-winged Black Tern Eagle Owl Collared Dove 114 Lopatar Lebada de vara Califar alb Rata pestrita Rata mare Rata caraitoare Rata lingurar Rata rosie Herete de stuf Uliu pasarar Sorecar comun Sorecar mare Vanturel rosu Vanturel de seara Soimul randunelelor Prepelita Fazan Gainusa de balta Lisita Scoicar Cataliga Ciocintors Pasarea ogorului Ciovlica ruginie Prundaras gulerat mic Ploier argintiu Nagat Fugaci roscat Fugaci de tarm Fluierar negru Fluierar cu picioare rosii Fluierar de zavoi Fluierar de mlastina Pescarus cu cap negru Pescarus mic Pescarus razator Pescarus rozalb Pescarus argintiu Pescarita razatoare Chira de mare Chira de balta Chirighita cu obraji albi Chirighita neagra Chirighita cu aripi albe Bufnita Gugustiuc 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 Streptopelia turtur (Linnaeus) Cuculus canorus Linnaeus Caprimulgus europaeus Linnaeus Apus apus (Linnaeus) Apus melba (Linnaeus) Merops apiaster Linnaeus Coracias garrulus Linnaeus Upupa epops Linnaeus Dendrocopos syriacus (Hemprich et Ehrenberg) Melanocorypha calandra (Linnaeus) Galerida cristata (Linnaeus) Alauda arvensis Linnaeus Riparia riparia (Linnaeus) Hirundo rustica Linnaeus Hirundo daurica Linnaeus Delichon urbica (Linnaeus) Anthus campestris (Linnaeus) Anthus spinoletta (Linnaeus) Motacilla flava flava Linnaeus Motacilla flava feldegg Michahellis Motacilla alba Linnaeus Luscinia luscinia (Linnaeus) Phoenicurus phoenicurus (Linnaeus) Saxicola rubetra (Linnaeus) Oenanthe oenanthe (Linnaeus) Oenanthe pleschanka (Lepechin) Turdus merula Linnaeus Acrocephalus shoenobaenus (Linnaeus) Acrocephalus scirpaceus (Hermann) Acrocephalus arundinaceus (Linnaeus) Hippolais pallida (Hemprich et Ehrenberg) Sylvya communis Latham Sylvya atricapilla (Linnaeus) Phylloscopus sibilatrix (Bechstein) Phylloscopus collybita (Vieillot) Phylloscopus trochilus (Linnaeus) Muscicapa striata (Pallas) Parus palustris Linnaeus Parus major Linnaeus Sitta europaea Linnaeus Oriolus oriolus (Linnaeus) Lanius collurio Linnaeus Lanius minor Gmelin Garrulus glandarius (Linnaeus) Pica pica (Linnaeus) Turtle Dove Cuckoo Nightjar Swift Alpine Swift Bee-eater Roller Hoopoe Syrian Woodpecker Turturica Cuc Caprimulg Drepnea neagra Drepnea mare Prigorie Dumbraveanca Pupaza Cocanitoare de gradini Calandra Lark Crested Lark Skylark Sand Martin Swallow Red-rumped Swalow House Martin Tawny Pipit Water Pipit Blue-headed Wagtail Black-headed Wagtail White Wagtail Thrush Nightingale Redstart Whinchat Wheatear Pied Wheatear Blackbird Sedge Warbler Reed Warbler Great Reed Warbler Olivaceous Warbler Ciocarlie de baragan Ciocarlan Ciocarlie de camp Lastun de mal Randunica Randunica roscata Lastun de casa Fasa de camp Fasa de munte Codobatura galbena Codobatura cu cap galben Codobatura alba Privighetoare de zavoi Codros de padure Maracinar negru Pietrar sur Pietrar negru Mierla Lacar mic Lacar de stuf Lacar mare Frunzarita cenusie Whitethroat Blackcap Wood Warbler Chiffchaff Willow Warbler Spotted Flycatcher Marsh Tit Great Tit Nuthach Golden Oriole Red-bached Shrike Lesser Grey Shrike Jay Magpie Silvie de campie Silvie cu cap negru Pitulice sfaraitoare Pitulice mica Pitulice fluieratoare Muscar sur Pitigoi sur Pitigoi mare Ticlean Grangur Sfrancioc rosiatic Sfrancioc cu frunte neagra Gaita Cotofana 115 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 Corvus monedula Linnaeus Corvus frugilegus Linnaeus Corvus corone cornix Linnaeus Sturnus vulgaris Linnaeus Sturnus roseus (Linnaeus) Passer domesticus (Linnaeus) Passer hispaniolensis (Temminck) Passer montanus (Linnaeus) Carduelis chloris (Linnaeus) Carduelis carduelis (Linnaeus) Carduelis cannabina (Linnaeus) Emberiza citrinella Linnaeus Emberiza schoeniclus (Linnaeus) Emberiza melanocephala Scopoli Miliaria calandra (Linnaeus) Jackdaw Rook Hooded Crow Starling Rose-coloured Starling House Sparrow Spanish Sparrow Tree Sparrow Greenfinch Goldfinch Linnet Yellowhammer Reed Bunting Black-headed Bunting Corn Bunting Stancuta Cioara de semanatura Cioara griva Graur Lacustar Vrabie de casa Vrabie negricioasa Vrabie de camp Florinte Sticlete Canepar Presura galbena Presura de stuff Presura cu cap negru Presura sura Table 2 - Bird species from Romanian Black Sea Coast (2008) No. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 Scientific Name Tachybaptus ruficollis (Pallas) Podiceps cristatus (Linnaeus) Podiceps grisegena (Boddaert) Podiceps nigricollis C.L.Brehm Phalacrocorax carbo sinensis (Linnaeus) Phalacrocorax pygmaeus (Pallas) Pelecanus onocrotalus Linnaeus Pelecanus crispus Bruch Botaurus stellaris (Linnaeus) Ixobrychus minutus (Linnaeus) Nycticorax nycticorax (Linnaeus) Ardeola ralloides (Scopoli) Egretta garzetta (Linnaeus) Casmerodius albus (Linnaeus) Ardea cinerea Linnaeus Ardea purpurea Linnaeus Ciconia ciconia (Linnaeus) Plegadis falcinellus (Linnaeus) Platalea leucorodia Linnaeus Cygnus olor (Gmelin) Anser anser (Linnaeus) Tadorna tadorna (Linnaeus) Anas strepera Linnaeus Anas crecca Linnaeus Anas platyrhynchos Anas querquedula English Name Little Grebe Great Crested Grebe Red-necked Grebe Black-necked Grebe Cormorant Pygmy Cormorant White Pelican Dalmatian Pelican Bittern Little Bittern Night-Heron Squacco Heron Little Egret Great White Egret Grey Heron Purple Heron White Stork Glossy Ibis Spoonbill Mute Swan Greylag Goose Shelduck Gadwall Teal Mallard Garganey 116 Romanian Name Corcodel mic Corcodel mare Corcodel cu gat rosu Corcodel cu gat negru Cormoran mare Cormoran mic Pelican comun Pelican cret Buhai de balta Starc pitic Starc de noapte Starc Galben Egreta mic Egreta mare Starc cenusiu Starc rosu Barza Tiganus Lopatar Lebada de vara Gasca de vara Califar alb Rata pestrita Rata mica Rata mare Rata caraitoare 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 Anas clypeata Netta rufina Aythya ferina Aythya nyroca Haliaeetus albicilla Circus aeruginosus Circus macrourus Circus pygargus Accipiter nisus Buteo rufinus Aquila pomarina Aquila clanga Hieraaetus pennatus Falco tinnunculus Falco vespertinus Falco subbuteo Perdix perdix Coturnix coturnix Phasianus colchicus Rallus aquaticus Porzana porzana Porzana parva Gallinula chloropus Fulica atra Haematopus ostralegus Himantopus himantopus Recurvirostra avosetta Burhinus oedicnemus Glareola pratincola Charadrius dubius Charadrius alexandrinus Vanellus vanellus Gallinago gallinago Limosa limosa Numenius arquata Tringa erythropus Tringa totanus Tringa stagnatilis Tringa ochropus Actitis hypoleucos Larus melanocephalus Larus minutus Larus ridibundus Larus genei Larus cachinnans Gelochelidon nilotica Sterna caspia Shoveler Red-crested Pochard Pochard Ferruginous Duck White-tailed Eagle Marsh Harrier Pallid Harrier Montagu’s Harrier Sparrowhawk Long-legged Buzzard Lesser Spotted Eagle Spotted Eagle Booted Eagle Kestrel Red-footed Falcon Hobby Grey Partridge Quail Pheasant Water Rail Spotted Crake Little crake Moorhen Coot Oystercatcher Black-winged Stilt Avocet Stone Curlew Collared Pratincole Little Ringed Plover Kentish Plover Lapwing Snipe Black-tailed Godwit Curlew Spotted Redshank Redshank Marsh Sandpiper Green Sandpiper Common Sandpiper Mediterranean Gull Little Gull Black-headed Gull Slender-billed Gull Yellow-legged Gull Gull-billed Tern Caspian Tern 117 Rata lingurar Rata cu ciuf Rata cu cap castaniu Rata rosie Codalb Herete de stuf Herete alb Herete sur Uliu pasarar Sorecar mare Acvila tipatoare mica Acvila tipatoare mare Acvila mica Vantirel rosu Vanturel de seara Soimul randunelelor Potarniche Prepelita Fazan Carstel de balta Crestet pestrit Crestet cenusiu Gainusa de balta Lisita Scoicar Cataliga Ciocintors Pasarea ogorului Ciovlica ruginie Prundaras gulerat mic Prundaras de saratura Nagat Becatina comuna Sitar de mal Culic mare Fluierar negru Fluierar cu picioare rosii Fluierar de lac Fluierar de zavoi Fluierar de munte Pescarus cu cap negru Pescarus mic Pescarus razator Pescarus rozalb Pescarus argintiu Pescarita razatoare Pescarita mare 74 75 76 77 78 79 Sterna sandvicensis Sterna hirundo Sterna albifrons Chlidonias hybridus Chlidonias niger Chlidonias leucopterus 80 81 82 83 84 85 86 87 88 89 90 91 Streptopelia decaocto Streptopelia turtur Cuculus canorus Athene noctua Asio otus Caprimulgus europaeus Apus apus Alcedo atthis Merops apiaster Coracias garrulus Upupa epops Dendrocopos major 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 Dendrocopos syriacus Melanocorypha calandra Galerida cristata Lullula arborea Alauda arvensis Riparia riparia Hirundo rustica Delichon urbica Anthus campestris Motacilla flava Motacilla alba Troglodytes troglodytes Erithacus rubecula Luscinia luscinia Luscinia megarhynchos Phoenicurus ochruros Phoenicurus phoenicurus Saxicola rubetra Saxicola torquata Oenanthe isabellina Oenanthe oenanthe Turdus merula Acrocephalus agricola Acrocephalus palustris Acrocephalus scirpaceus Acrocephalus arundinaceus Hippolais pallida Sandwich Tern Common Tern Little Tern Whiskered Tern Black Tern White-winged Black Tern Collared Dove Turtle Dove Cuckoo Little Owl Long-eared Owl Nightjar Swift Kingfisher Bee-eater Roller Hoopoe Great Spotted Woodpecker Syrian Woodpecker Calandra Lark Crested Lark Woodlark Skylark Sand Martin Swalow House Martin Tawny Pipit Blue-headed Wagtail White Wagtail Wren Robin Thrush Nightingale Nightingale Black Redstart Redstart Whinchat Stonechat Isabelline Wheatear Wheatear Blackbird Paddyfield Warbler Marsh Warbler Reed Warbler Great Reed Warbler Olivaceous Warbler 118 Chira de mare Chira de balta Chira mica Chirighita cu obraji albi Chirighita neagra Chirighita cu aripi albe Gugustiuc Turturica Cuc Cucuvea Ciuf de padure Caprimulg Drepnea neagra Pescaras albastru Prigorie Dumbraveanca Pupaza Ciocanitoare pestrita mare Ciocanitoare de gradini Ciocarlie de baragan Ciocarlan Ciocarlie de padure Ciocarlie de camp Lastun de mal Randunica Lastun de casa Fasa de camp Codobatura galbena Codobatura galbena Ochiuboului Macaleandru Privihetoare de zavoi Privighetoare roscata Codros de munte Codros de padure Maracinar mare Maracinar negru Pietrar rasaritean Pietrar sur Mierla Lacar rasaritean Lacar de mlastina Lacar de stuf Lacar mare Frunzarita cenusie 119 120 121 122 123 124 125 126 127 128 129 130 131 132 Sylvia nisoria Sylvia curruca Sylvia communis Sylvia borin Sylvia atricapilla Phylloscopus collybita Phylloscopus trochilus Muscicapa striata Ficedula albicollis Panurus biarmicus Parus palustris Parus caeruleus Parus major Certhia brachydactyila 133 134 135 136 137 138 139 140 141 142 Oriolus oriolus Lanius collurio Lanius minor Garrulus glandarius Pica pica Corvus monedula Corvus frugilegus Corvus corone cornix Sturnus vulgaris Sturnus roseus 143 144 145 146 147 148 149 150 151 152 153 Passer domesticus Passer hispaniolensis Passer montanus Fringilla coelebs Carduelis chloris Carduelis carduelis Carduelis cannabina Emberiza citrinella Emberiza hortulana Emberiza schoeniclus Miliaria calandra Barred Warbler Lesser Whitethroat Whitethroat Garden Warbler Blackcap Chiffchaff Willow Warbler Spotted Flycatcher Collared Flycatcher Bearded Tit Marsh Tit Blue Tit Great Tit Short-toed Treecreeper Golden Oriole Red-backed Shrike Lesser Grey Shrike Jay Magpie Jackdaw Rook Hooded Crow Starling Rose-coloured Starling House Sparrow Spanish Sparrow Tree Sparrow Chaffinch Greenfinch Goldfinch Linnet Yellowhammer Ortolan Reed Bunting Corn Buntng Silvie porumbaca Silvie mica Silvie de campie Silvie de zavoi Silvie cu cap negru Pitulice mica Pitulice fluieratoare Muscar sur Muscar gulerat Pitigoi de stuf Pitigoi sur Pitigoi albastru Pitigoi mare Cojoaica cu degete scurte Grangur Sfrancioc rosiatic Sfrancioc cu frunte neagra Gaita Cotofana Stancuta Cioara de semanatura Cioara griva Graur Lacustar Vrabie de casa Vrabie negricioasa Vrabie de camp Cinteza Florinte Sticlete Canepar Presura galbena Presura de gradina Presura de stuf Presura sura This show that in the period of study (april-august 2008), a number of 172 species of birds have been observed on the sea coast between Cape Midia and Cape Kaliakra (Romania-Bulgaria). In Romania (the sea coast between Cape Midia and Vama Veche), 153 species of birds have been seen. In Bulgaria (the sea coast between Durankulak and Cape Kaliakra), 121 speces of birds have been observed. A number of 42 species of birds have been seen only on the Romanian litoral, while 19 bird species have only been witnessed on the Bulgarian litoral. Because most of my time has been spent on the Romanian sea side, it is only natural that the number of species identified here will be larger that the one from Bulgaria, because there exist common birds, which is impossible not to appear on the Bulgarian sea coast, because the migration follows both the Romanian and the Bulgarian coast-line. Species as Tachybaptus ruficollis, Podiceps griseigena, Podiceps nigricollis or Gallinago 119 gallinago, Limosa limosa, Numenius arquata, Charadrius alexandrinus, identified on the Romanian coast, will surely pass during migration on the Bulgarian litoral. This is also available for a number of species from Bulgaria, as the Gavia arctica,, Buteo buteo, Burhinus oedicnemus, Pluvialis squatarola, Tringa glareola, Caprimulgus europaeus, Acrocephalus schoenobaenus, which were identified on the sea coast in past years but have not been observed in the study period. In the north of the study area (Romania) some aquatic bird species also appear during summer-time, arriving from the nesting places in the Danube Delta and from Razelm-Sinoe lagunas, which we have not been able to identify on the Bulgarian litoral: Pelecanus onocrotalus, Pelecanus crispus, Plegadis falcinellus si Anser anser. Moreover, the number of birds of prey species (Falconiformes) is considerable larger in Romania than in Bulgaria (12, respectively 7). Rocky cliff ecosistems from Bulgaria and the lack of antropic impact lead to species living here not able to be seen on the Romanian litoral. One of this species is Phalacrocorax aristotelis (Shag). We have only witnessed this bird on the sea and on the marine cliffs from Cape Kaliakra, Bolata Dere and Rusalka. The species prefers the sea and rocky cliffs and only occasionally appears on the Romanian sea side. The motif is the lack of rocky cliffs (non-existent on the Romanian littoral) and the extremely powerful anthropic impact on the Romanian coast. The birds are still nesting in the area of Bulgaria rocky cliffs in tens of mates. Another species which is not found on the Romanian littoral is Apus melba (Alpine swift). During the study period, we have only met this birds at Kavarna, Cape Kaliakra and Bolata Dere. A nesting colony exists in Kavarna on the sea-oriented wall of the spectaculous Cerahman Hill (10-12 mates). A swallow rare in Romania is the Hirundo daurica (Red-rumped Swallow) seen in the study area at Yaylata (Kamen Briag), Rusalka, but especially in the Bolata Dere canyon (probably it’s nesting place). The lack of rocky walls for the birds to nest in leads to the disappearance of it’s area before the Romanian-Bulgarian border. Oenanthe pleshanka (Pied Wheatear) is frequently met on the on the marine rocky cliffs of Bulgaria: Yaylata, Rusalka, Bolata Dere and Cape Kaliakra, where it also nests. It is entirely missing from the romanian littoral. Another species that can commonly be found in the area of lake Durankulak and lake Sabla is Passer hispaniolensis (Spanish Sparrow). If it is more frequent here (it nests in the lake surroundings) and is more numerous then Passer montanus (Tree Sparrow) and Passer domesticus (House Sparrow), past the RomanianBulgarian frontier, the situation is opposite, the most numerous being Passer domesticus followed by Passer montanus, and Passer hispaniolensis is entirely missing from the Romanian littoral. Emberiza melanocephala (Black-headed Bunting) is another bird frequently found between Durankulak and Yaylata (Kamen Briag) where it also nests. On the Romanian littoral, the species is rarely found, probably because the human impact causing an accentuated degradation of the habitat. We must state that some species, as the Hirundo daurica, Oenanthe pleshanka and Passer hispaniolensis, even if they don’t appear on the Romanian sea-coast, penetrated Dobrogea through the south-west, in the Canaralelor area from Baneasa, where these birds have found favorable habitats, coming up from the north towards and reaching Cheile Dobrogei and even Macin Mountaines. In July 2008 we had the chance to see the migration of the Riparia riparia (Sand Martin) on the Bulgarian sea coast. We estimated about 14 000 birds passing from north to south on 18-20.07.2008. On the Sabla lake, on 20.07.2008, was 10 000 sand martins. Most of this birds are protected by the international laws, like the Birds Directive – European Council Directive 79/409 EEC – Annex I (Table 3): 120 Table 3 - Bird Species from Eastern Bulgarian Black Sea Coast (2008) Birds Directive (European Council Directive 79/409 EEC) Annex I No. Scientific Name English Name Romanian Name 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 Gavia arctica (Linnaeus) Phalacrocorax carbo sinensis (Linnaeus) Phalacrocorax aristotelis (Linnaeus) Phalacrocorax pygmaeus (Pallas) Botaurus stellaris (Linnaeus) Ixobrychus minutus (Linnaeus) Nycticorax nycticorax (Linnaeus) Ardeola ralloides (Scopoli) Egretta garzetta (Linnaeus) Casmerodius albus (Linnaeus) Ardea purpurea Linnaeus Ciconia nigra (Linnaeus) Ciconia ciconia (Linnaeus) Platalea leucorodia Linnaeus Aythya nyroca (Guldenstadt) Circus aeruginosus (Linnaeus) Accipiter nisus (Linnaeus) Buteo rufinus (Cretzschmar) Haematopus ostralegus Linnaeus Himantopus himantopus (Linnaeus) Recurvirostra avosetta Linnaeus Burhinus oedicnemus (Linnaeus) Glareola pratincola (Linnaeus) Tringa glareola Linnaeus Larus melanocephalus Temminck Larus genei Breme Gelochelidon nilotica (Gmelin) Sterna sandvicensis Latham Sterna hirundo Linnaeus Chlidonias hybridus (Palllas) Chlidonias niger (Linnaeus) Bubo bubo (Linnaeus) Caprimulgus europaeus Linnaeus Coracias garrulus Linnaeus Dendrocopos syriacus (Hemprich et Ehrenberg) Melanocorypha calandra (Linnaeus) Anthus campestris (Linnaeus) Lanius collurio Linnaeus Lanius minor Gmelin Black-throated Diver Cormorant Shag Pygmy Cormorant Bittern Little Bittern Night-Heron Squacco Heron Little Egret Great White Egret Purple Heron Black Stork White Stork Spoonbill Ferruginous Duck Marsh Harrier Sparrowhawk Long-legged Buzzard Oystercatcher Black-winged Stilt Avocet Stone Curlew Collared Pratincole Wood Sandpiper Mediterranean Gull Slender-billed Gull Gull-billed Tern Sandwich Tern Common Tern Whiskered Tern Black Tern Eagle Owl Nightjar Roller Syrian Woodpecker Cufundar polar Cormoran mare Cormoran motat Cormortan mic Buhai de balta Starc pitic Starc de noapte Starc galben Egreta mica Egreta mare Starc rosu Barza neagra Barza alba Lopatar Rata rosie Herete de stuf Uliu pasarar Sorecar mare Scoicar Cataliga Ciocintors Pasarea ogorului Ciovlica ruginie Fluierar de mlastina Pescarus cu cap negru Pescarus rozalb Pescarita razatoare Chira de mare Chira de balta Chirighita cu obraji albi Chirighita neagra Bufnita Caprimulg Dumbraveanca Cocanitoare de gradini Calandra Lark Tawny Pipit Red-bached Shrike Lesser Grey Shrike Ciocarlie de baragan Fasa de camp Sfrancioc rosiatic Sfrancioc cu frunte neagra 36 37 38 39 121 We can sea easily that a large number of species of birds are protected by this important European law. That means the study area is very important for this protected birds. All this species are present also on the Romanian litoral. Conclusions In Romania the anthropical impact is very heavy for the populations of birds (especially in the summer). For this reason, here, the number of nesting birds is very poor. In Bulgaria, it is a less anthropical impact, the area is not affected by the people. In Bulgaria still exist an important number of nesting birds. The habitats are different in the two countries: in Romania are especially sand beaches and in Bulgaria are especially rocky cliffs. That means some species are seen only on the Bulgarian sea coast. The whole area is very important for the migratory birds. Here it is a major way for them. In winter, the human impact is not so important, that means the area is also an importat wintering area. The preservation of the Bulgarian sea coast is very important, because in Romania the littoral is already affected by the tourism. In Romania, the most important wetlands from the sea-coast are Techirghiol Lake and Hergheliei (Mangalia) Swamp. Here we can find the bigger number of species of birds (and the large number of birds, too). We have seen 172 species of birds in the study area – a large avifaunistical diversity. For the future, it is very important to study the relations between the people and birds, in order to make possible the survival of the men and birds. References 1. 2. 3. 4. 5. 6. 7. B NICA, G., 1996 – Contributii la studiul avifaunei lacului Techirghiol, Lucrarile celei de-a treia conferinte nationale pentru protectia mediului prin metode si mijloace biologice si biotehnice, Universitatea “Transilvania”, Brasov: 376-379. B NICA, G., 2000 - Mlastina Hergheliei, Buletin A.I.A., nr. 9, S.O.R., Cluj-Napoca:2. BRUUN, B., DELIN, H., SINGER, A., 1999 – Pasarile din Romania si Europa, S.O.R., Hamlyne Guide, Octopus Publishing Group Ltd., London. MUNTEANU, D., TONIUC, N., WEBER, P., SZABO, J., MARINOV., 1989 - Evaluarea efectivelor pasarilor acvatice in cartierele lor de iernare din Romania, Ocrotirea Naturii si a Mediului Inconjurator, t. 33, 2, Bucuresti: 105-112. MUNTEANU, D., 1998, Dictionarul poliglot al speciilor de pasari din Romania, Editia a II-a, Pblicatiile S.O.R. nr.6, Cluj-Napoca. PETERSON, R., MOUNTFORT, G., HOLLOM, P., A., D., 1989 – Guide des oiseaux d’Europe, Ed. Delachaux et Niestle, Paris. SVENSSON, L., MULLARNEY, K., ZETTERSTROM, D., GRANT, P., 2000 – Le Guide Ornitho, Ed. Delachaux et Niestle, Paris. THE ORNITHOFAUNA OF SEASIDE BULGARIAN DOBROUDJA Stoyan NONEV Regional Museum of History – Dobrich, Department “Nature”, “Konstantin Stoilov ”str. 18, P.B. 131, 9300 – Dobrich, Bulgaria __________________________________________________________________________________________ Abstract: The aim of the paper is the ornithological evaluation of the territory of the coastal Bulgarian Dobroudja, the presentation of typical species of nesting birds from the coastal steppe areas and the water birds in the humid zones of the Lakes Shabla and Durankulak, Another aim is the presentation of some bird species not typical for this territory that hibernate in south, passing trough this part of the Dobrudja. Keywords: ornithofauna, Bulgarian Dobroudja, seaside, nesting birds, steppe areas, humid zones. __________________________________________________________________________________________ Introduction Dobroudja, named in the antiquity Scythia Minor is historical-geographic region, situated in the NorthEast part of the Balkan Peninsula. On the north and north-west bordered by the river Danube, on the east by Black Sea, and on the south by Batovska river. Bulgarian Dobroudja now is divided in two parts North and South Dobroudja. Seaside Dobroudja has not so good expressed borders. She started with the territories of the municipalities Balchik, passing over the municipality Kavarna, Shabla and ended by the state border with Romania. The terrain is almost flat, come on with the elevation “0”. On some places is cutting by little gullies, part of the coast is rocky, with caves, which disrupt the flat character of the land. There are two big firth lakes, Shabla and Durankulak, as well as three hyperhalline reservoirs /tuzlas/, which are very important for the concentration of the ornithofauna of the region. The climate of Bulgarian Dobroudja is temperate to transitional continental. The coastal area belongs to the continental- Mediterranean climatic region and characterized as a proximately mild winter and hot, dry summer. The coastal area belongs to the continental- Mediterranean climatic region; during the summer the maximum air temperatures are lower, and during the winter they are above 0, the snow cover is unstable. Strong north and north-east winds prevail. They are often accompanied by abundant snow falls and icing. Natural vegetation has been significantly altered due to the long-term anthropogenic effect. Natural environment is preserved only in single small locations not included in agricultural activities. The region is characterized with xerothermic oak forests (with admixes of elm, hornbeam, etc.), lime-tree forests, and various species of xerothermic grass communities. The northernmost flooded forest, Baltata, is also located in this region. Secondary growth of Oriental hornbeam and (Jerusalem) Christ thorn can be observed, as well. On the whole, the Dobroudja region is a typical agrarian area. Under the influence of the people the firmer forests are vanished and transformed their landscape, looking like steppe. In 50-th years of the future century, the steppes are ploughed up and reduce into agriculture areas. In the same time was formed the forest shelter belts to protect the fields from the hard north winds as well during the winter as during the summer (dry winds). All these works are to restrict the erosion of the fruitful level of the soil and to keep the snow-cover during the winter. The forest shelter belts are very important for the forming of the nest ornithofauna of the region, and also for the bird migration. The fauna is represented by Euro-Siberian and European species. The region is rich in steppe species, both animals and plants. They are widespread mostly in the eastern part of the territory. On the lands of Kavarna municipality two nature-archaeological reserves Kaliakra and Jailata are situated, and in Shabla municipality - protected natural areas Shabla lake, Shablenska tuzla and Durankulak lake. Between the village of Balgarevo, cape Kaliakra and Eni Kulak area are the best preserved typical steppe communities in Dobroudja. The steppes here are the largest and in best conditions. Typical for these biotopes are species, like 123 short-toed lark (Calandrella brachydactyla), calandra lark (Melanocorypha calandra), black-headed bunting (Emberiza melanocephala), different species of wheatear (Oenanthe) and isabellina-weatear (Oenanthe isabellina) and Stone-Curlew (Burhinus oеdicnemus) among them. Here some rare species - Eagle-owl (Bubo bubo) and Long-legged Buzzard (Buteo rufinus) also nidificate. Nesting populations of these typical for the steppe species are best presented on this confined space. The area between Tyulenovo and Kaliakra is well known from the specialists and fans like a place, where a most beautiful and uncommon pink starlings (Stumus roseus) can be seen. These “wanderers” of the steppes are staying and nesting here only if they have enough nutritive value. Otherwise the flocks migrate to the south toward Turkey, or move to the north toward Rumania and Ukraine. The cape Kaliakra is the most eastern point of this seacoast. He is extremely important for the migratory birds. The region is famous as a medial station for a great amount of migratory birds along the Black Sea coast. It is known long ago, that here alight coveys of white storks and, quails and many little songbirds for a rest. During this period here feed migratory small birds of prey: harrier, falcons, hawks. When bad climatic conditions appears, the aquatoria around the bay, give shelter to the migrating, hibernating and aquatic birds. Sometimes here can be observed hundreds of loons, wild ducks, mallards etc. heaping. On the rock cornice from Kaliakra to Tyulenovo nested also the aristotelis cormorant (Phalacrocorax aristotelis). In spite of this, it is considered as vulnerable and is included to the new Red list of the species in this category. Therefore, this strategic for the birds region and especially the Kaliakra cape uses to be quite like a magnet for the ornithologists. No matter of the already existing large information over the bird species, found in this aria during different seasons, the parameters of the nest communities in this biotope is not well known. In spite of the permanent narrowing of this typical for Dobroudja landscape, it is necessary to make description of the here nesting birds’ populations, starting from an investigation of the possibilities for enlargement of the already existing reserve Kaliakra. With the help of the Bulgrian - Switzerland Programme, during the year 1996 a lot of similar surveys have been done by Bozhidar Enchev and Stoyan Nonev. Material and Methods During the nesting season in 1996 three reports concerning the nesting birds in the region have been made. For that purpose, five different in their vegetation substance and ground structure, sectors has been determined. • Typical for the Kaliakra steppe. With grass coverage to height of 10-12 centimeters. Average count of vegetation stalks above the medium height – 66,24m2. Stone coverage – approx.10-20%. Single bushes - here and there within the sector. Separate groups of trees (pine, oleaster and others) along the road Bulgarevo village – Cape Kaliakra. On this platform a stone-pit near Cape Zelenka is also situated. Through it passes a power transmission line constructed from cement and metal columns. Here also 40 goats and 240 sheep graze. Area – 73 hectare. • Area with cadastre number № 128 to the south of the Eni kulak countryside. Here the grass is with different height and it forms mosaic spots from 10 to 50 centimeters. The average height is from 18 to 20 centimeters. Average count of vegetation stalks above the medium height – 457,28m2. However the grass seems to be loose, because of the fact that the high grasses are the stalks of the wheat plants indeed. Stones – 10%. Area – 26,2hectare. Extremely well preserved steppe. No trace of a human influence. • Steppe bushy area, overgrown with hornbeam, oak, sumac, wild briar, hawthorn and ashl trees. The height of the bushes riches 3m. Coverage about 40%. Between the bushes there is typical steppe vegetation, the same as in sector №1. Area - 30 hectare. • Cape Kaliakra: from the first fortress wall to the cape (cadastre numbers 293, 296, 298,299). This sector is full of variety. The biggest part of the area is occupied with archaeological excavations. Among them there is exuberant, thick grass vegetation, and single low bushes. In the front part of the of the cape there are several buildings for living and around them and along the edge of the rock there are some 124 • group of trees and some single ones, thick bushes and several cypresses. A small number of open rock caves are also situated in this sector. Area – 26,5 hectare. A sector, located to the south of the Eni kulak countryside; between the Eni kulak, the strip of a land over the sea and the Bolata gulch. The average height is from 20 to 30 centimeters. Average count of vegetation stalks above the medium height – 100,8m2. Groups of thorn bushes, oak, ashl tree, wild briar and hornbeam and others. Coverage about 20%. There are areas without stones at all, total coverage – about 10%. Area – 16 hectare. For the determination of the number of the nidificating couples the map-making method was used. It gives the best possible results in such territories. Results and Discussions During the nesting season in 1996 in the steppes of the plateau of cape Kaliakra 32 species of nidificating birds were found. In this number we don’t include those that inhabit rock perches (12 species), 6 more additional species connected with some specific bio-zones in Bolata, as well as those, feeding in the steppe. We will discuss them separately. The location of the species in different sectors and the density of their populations are put in tables 1-5. On the fist sector the greatest number of nidificating birds was found (Table 1). The bigger part of those species nests on the ground (7 species) or in halls in the ground (6 species). Prevailing species here are the larks (Melanocorypha calandra, Calandrella brachydactyla and the Wood-lark). The availability of some hollow cement columns makes possible the nesting of the starling, the sparrow and the blue crow too. Table 1 - Number and density of the nesting birds in the sector №1 /Steppe on the East of Bulgarevo village, 73 hectares № 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 Species Melanocorypha calandra Calandrella brachydactyla Alauda arvensis Oenanthe oenanthe Anthus campestris Galerida cristata Sturnus vulgaris Oenanthe pleschanka Oenanthe isabellina Lanius minor Upupa epops Miliaria calandra Burhinus oedicnemus Emberiza melanocephala Lanius collurio Merops apiaster Falco tinnunculus Carduelis cannabina Coracias garrulus Number of nesting birds 33 27 23 14 8 8 8 7 6 5 5 4 3 3 3 3 2 1 1 125 Density of couples/10ha 4,52 3,7 3,15 1,92 1,1 1,1 1,1 0,96 0,82 0,68 0,68 0,55 0,41 0,41 0,41 0,41 0,27 0,14 0,14 20 Passer domesticus 21 Pica pica 22 Strptopelia decaocto Total 1 1 1 167 0,14 0,14 0,14 22,88 The magpie makes its nests not only on the trees but in bushes near the road and on the metal parts of the electrical columns as well. After that the kite uses those same nests. The presence of the turtle-dove is not typical, having in mind the fact that its nest is situated on the black pine tree near the road. The sector № 2 is nothing but one typical for the steppes grass community where there aren’t almost any bushes and no pasture at all. Almost identical conditions in the entire area allows here to nidificate only limited number of birds. They are adapted to the open air-spaces and they nest on the ground. Their thickness here is vastly higher in comparison with the other sectors (table 2). Table 2 - Number and density of the nesting birds in the sector №2/cad. №128; 26,2 ha № 1 2 3 4 5 6 7 8 Species Melanocorypha calandra Alauda arvensis Calandrella brachydactyla Miliari calandra Emberiza melanocephala Anthus campestris Burhinus oedicnemus Lanius collurio Total Number of nesting birds 33 11 6 2 2 1 1 1 57 Density of couples/10ha 12,60 4,20 2,29 0,76 0,76 0,40 0,40 0,40 21,76 The small number of single bushes limits the presence of the inhabiting species to two – Emberiza melanocephala and Lanius collurio. Along the Bolata gulch a bio-zone is differentiating. It differs from those we have determined as typical steppe. (sector №1) Here increases the number of the bushes, they are much higher and they make groups with vastly coverage. In this way, some conditions for nesting of additional number of species not typical for steppe region origin. (table3) Table 3 - Number and density of the nesting birds in the sector №3/ thin bushes entering the “Bolata” object; 30 ha/ № 1 2 3 4 5 6 Species Miliaria calandra Emberiza melanocephala Alauda arvensis Carduelis cannabina Lanius minor Melanocorypha calandra Number of nesting birds 6 3 2 2 2 2 126 Density of couples/10ha 2,0 1,0 0,7 0,7 0,7 0,7 7 8 9 10 11 12 Sylvia nisoria Galerida cristata Hippolais pallida Pica pica Sylvia communis Upupa epops Total 2 1 1 1 1 1 24 0,7 0,3 0,3 0,3 0,3 0,3 8,0 That’s why we divide the sector in this bio-zone, nevertheless that it is inseparable part of the landscape as a whole. Although the larks inhabit this sector too, their number here is vastly smaller. Here we can find the great number of Emberiza calandra. It prefers this bio-zone because it uses the top of the bushes from where it marks its territory. Typical for this area is also the Emberiza melanocephala. Some two other species of garden warbler appears and they also prefer thin bushes. Because of the lack of high trees here the magpie also nests. The sector №4 has its specific characteristics and it differs thoroughly from the main part of the region. That’s why here is settled a community including a great variety of species and part of them are sparrows and swallows (table 4). Table 4 - Number and density of the nesting birds in the sector №4/ from the firs fortress wall to the cape Kaliakra, cad. №293, 296, 298 and 299, 26,5 ha № 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 Species Number of nesting birds Density of couples/10ha 15 11 7 5 5 3 3 2 2 2 2 2 1 1 1 1 1 1 65 5,66 4,25 2,64 1,89 1,89 1,13 1,13 0,75 0,75 0,75 0,75 0,75 0,38 0,38 0,38 0,38 0,38 0,38 24,53 Oenanthe pleschanka Passer domesticus Emberiza melanocephala Miliaria calandra Oenanthe oenanthe Carduelis cannabina Passer montanus Galerida cristata Lanius collurio Parus major Passer hispaniolensis Upupa epops Anthus campestris Athene noctua Carduelis carduelis C. chloris Hippolais pallida Sylvia communis Total On this sector, in the existing caves also 8 more couples of swallows are nesting. 127 The most numerous species here is the black-backed wheatear and this is predetermined from the fact that there are a lot of stone walls and holes in the rocks. The next one is the sparrow. It also finds here the optimum conditions for nesting in the already existing buildings and for feeding – in the surrounding grass areas. The greater part of the species is presented here with the small number of couples. Natural platform №5 is situated along the coast. The grass here is high and the bushes are gathered in small groups. Table №5. Number and density of the nesting birds in the sector №5/ between the Eni kulak and the Bolata gulch, 16 ha № 1 2 3 4 5 6 7 Species Melanocorypha calandra Miliaria calandra E. melanocephala Oenanthe pleschanka Alauda arvensis Carduelis cannabina Lanius collurio Total Number of nesting birds 17 4 3 3 2 2 1 32 Density of couples/10ha 10,6 2,5 1,9 1,9 1,2 1,2 0,6 20,0 The great number of Melanocorypha calandra (Table 5) and the absence of the Calandrella brachydactyla is determined from the high grass here. In the west the grass became lower and the steppe starts to carry the characteristics of the sector №1. Here the count of the Calandrella brachydactyla is much higher (50 couples) than the number of the Melanocorypha calandra (10 couples). In the researched territory 3 couples of nesting partridge were found. The density of this species have been calculated, having in mind the whole territory of the area and it is 0, 04 couples per 10 hectares. Conclusions During the period 1978-79 a survey concerning the territory and the number of the Phalacrocorax aristotelis have been made by expert-curators from the Regional Museum of History – Dobrich. On the vertical rock formations near Tulenovo village and Kaliakra cape about 40 couples of these birds have been found with an annual population increase of 7 to 10 nests (baby birds). Today (2007) we can find here about 180-250 couples of the Phalacrocorax aristotelis, or we may say that the number of the birds increases and the species is stable. But we couldn’t say such kind of words for the Burhinus oеdicnemus. The pasture here is not enough and the height of the grass is three or four times bigger than the height of the Burhinus oеdicnemus. This fact breaks the conditions which assure the existing of the species. And if we put in addition the facts that the density of the Canis aureus and Elarus agentatus on this territory increases as well the presence of the rambling dogs, the great number of buildings that appears and the wind generators in the area, we may certainly say that the population of this species is threatened with extinction. Now the information needs to be refreshed, especially because of the coming changes in steppe communities – result of the wind generators constructing. The steppes of the seaside Dobroudja are turning into wet zones on the territory of Shabla and Durankulak. The Shabla Lake is declared as protected zone from the year of 1979. Inseparably part of the Shabla Lake complex is the Shablenska tuzla. This complex is one of the most well kept from anthropogenic influence wetland on the Black Sea coast. The Shabla and Durankulak lakes are included in the European Program Burd Life International - ornithological important places. The Durankulak Lake is declared as natural landmark during 128 the year 1980. Because of the fact, that they are keeping definite quantities of the aquatic birds, they are reported for Ramsar places under Ramsar convention, with Bulgaria as a side in it. The lakes play a certain part during the migration of the birds and especially in winter time. Practically the whole population, about 56 000 representatives, of the world threatened with extinction red gizzard goose (Branta ruficollis) hibernates here. Big quantities from the white frontlet goose (Anser albifrons), different types of mallards, swans and others also find a shelter here, during the winter. The role of the lakes and the shores increases vastly, when the weather in the Danube Delta is getting worse and the swamps are frozen. By such meteorology conditions our lakes are full of birds. The nesting ornithofauna is represented with 57 species, 10 from them are rare. Here can be found the border west area of the territories occupied with India warbler (Acrocephalus agricola). Because of these, there are tourists, very found of birds, coming from whole Europe. In the Durankulak Lake, during the migration, periodically one rare species, also can be found. This is the Stiff-tailed duck (Oxyura leucocephala) - an object of international project which is after its protection. Durankulak is the next station on its migration way to Greece after the Rumanian lakes in Dobroudja. During the last years, the natural communities in Dobroudja are subjects of powerful anthrop-genetic pressure. There are almost no remains from the steppe biotopes in the region. In them a number of characteristic species are found, which because of the coming changes, quick and precipitously reduce their quantity. The steppes are from a great significance for the migration for some distinct species. Here they rest and feed. That’s why their protection is very urgent. The question for the possible reintroduction of some species also needs detailed investigation. It is necessary to examine suitable terrains and to work out a similar program, in which specialists at large, representatives of state and NGOs to be able to take part. The Seaside Dobroudja, possesses varied and interesting ornithofauna. The natural diversity of Dobroudja in every season and the fact that this region is on the Black Sea migration way of the birds, are giving extremely good possibilities for development of ecology and alternative tourism in any time of the year. Utilization of this opportunity and the protection of the wild nature must be the utmost task for the municipalities and the local public. References 1. NONEV, S, 1978. Observation on the nesting and number of the Phalacrocorax aristotelis on the territory of the Dobrudja seaside 1975-1977. Orn. Inf. Bul., 3,11-13. 2. SIMEONOV, S., MICHEV, T., NANKINOV, D., 1990. Fauna of Bulgaria. Aves, vol. 1, BAN, S., 350p. 3. BOTEV, B. & TZOLO PESHEV (EDS.), BOEV N., SIMEONOV S., BESHKOV V., KARAPETKOVA M., POMAKOV V., MICHEV, T., 1984 - Red Data Book of the People’s Republic of Bulgaria, Volume 2. Animals, Publishing House of the Bulgarian Academy of Sciences, Sofia. 4. IANKOV, P. (Ed.) 2007. Atlas of breeding birds in Bulgaria.-Bulgarian Society for the Protection of Birds, Conservation series, Book 10, Sofia, BSPB, 56-57. 5. IVANOV, B. E., NONEV, S. I., 1997. Scientific reports “Dobrudja and Kaliakra”, VSI, Plovdiv 6. PETROV, B.M., ZLATNOV, S. I., 1955. Materials for the fauna of the Dobrudja’s birds, Magazine of the Scientific Institute at the Ministry of Agriculture, book 1, 93-111pp. 7. NONEV,. S., 1977. Pastor roseus L. in Dobrudja. Orn. Inf. Bul., 10-14. 8. SIMEONOV, S., MICHEV, T., 1985. Population of Bubo bubo L. in Bulgaria. Ecology, 15, 60-65pp. 9. BAUMGART, W. 1970. Ueber die Voegel im Kuestengebiet der suedlichen Dobrudscha (Silberkueste), Der Falke, 17, 220-231. 10. BIBBY, C., BURGESS, N., HILL, D., 1992. Bird census techniques. Academic Press, London, 257pp. 129 STUDY OF THE POLYCHAETA FAUNA (ANNELIDA) FROM THE MEDIOLITTORAL AND INFRALITTORAL OF THE BLACK SEA: LITTORAL SEGMENT CAPE MIDIA – CAPE KALIAKRA Gabriela - Mihaela PARASCHIV* * Universitatea Ovidius Constanţa, Facultatea de Ştiinţe ale Naturii şi Ştiinţe Agricole B-dul Mamaia, nr. 124, Constanţa, 900527, Romania, gmparaschiv@gmail.com __________________________________________________________________________________________ Abstract: Polychaeta represent an important component of the marine benthos by the number of species, the density of the abundance and biomass recorded in various benthic biocenosys of the Pontic basin. Our research subject area is characterized by the existence of a mosaic of habitats, from the sedimentary ones, from the sheltered areas of the beach protection breakwaters or port premises (reported on the Romanian seaside length), to the ones made up from platform exposed to the direct wave action from Vama Veche; from those encountered in the low depth (mediollittoral and infralittoral) to the sedimentary and shell-type substrate from 15 or 25 meters deep (Constanta and Cap Kaliakra). Community best represented by Polychaeta is the one from the hard substrate habitats of all the horizons of depth, where there are encountered vagile forms of the Palpata, as well as tubicolous forms of Scolecida group, with sedentary lifestyle and detritivorous-filtrates or sedimentfeeding style. Keywords: polychaeta community, benthic fauna, sedimentary, hard and phytal substratum __________________________________________________________________________________________ Introduction Fauna of polychaeta group from the Mediterranean-Pontic basin includes approximately 400 species, ie 5% of the total number of polychaeta species known until today; for the Black Sea are quoted from this group 199 species, which is 49.5% of Mediterranean polychaeta fauna and 2.5% of the species cited in Planetary Ocean. Structural changes reported in recent years at Planetary Ocean communities level led experts to conduct studies on benthic wildlife in general and thus of the polychaeta; these studies followed a reassessment of the taxonomic lists from various geographical regions, and especially particularly studies focusing on specific biogeography of specific and supra-specific taxons and on their distribution at regional level, depending on the main category of substrate. Concerning for polychaeta bio-geography knowledge has become a concern because it has identified some species or habitats in regions that previously had not been reported or others report the disappearance of habitats in which another time it was considered characteristic (Bartolomaeus, 2005; Bellot, 2004; Musco, 2005; Glasby, 1999, 2005). In this context, we mention the research conducted by (Sergheva, 1998; Kisseleva, 1968, 1985) on the fauna of anoxic biotopes of the Black Sea which quotes a new species for science – Vigtoriella zaikai KISSELEVA (Sergheva, 1998) and a new species for the Black Sea of the genus Protodrilus HATSCH; representatives of this genus, Protodrilus (other species than P. flavocapitatus ULIJ) have been identified by us too in different habitats of the north-western of the Pontic basin from 50-60 m depth. In the category of species which lately have not been reported in mediollittoral habitats, with gross sediments from the south of Constanta, are Ophaelia bicornis SAVIG and Praegeria remota SOUTH. (B cescu, 1972; Paraschiv and Gomoiu, 2002; Paraschiv, 2006) or in the infralittoral sedimentary habitats: Arenicola marina L. (Gomoiu, 1981) Material and Methods Our study is based on several categories of data obtained by us during 2002-2006 periods (Fig. 1): - 57 samples from small depth community (mediollittoral and infralittoral), and - 20 samples obtained through 130 research carried out in the research programs: GEF/Akademik Cruise-2003 and GEF/Parshin Cruise CERES2005 and CERES 2006. C. Midia – C. Kaliakra Littoral Zone Medio- and infralittoral Sits (0-5 m) Transects Constanta C. Midia, C.Kaliakra Fig. 1 – Researched area: Cape Midia – Cape Kaliakra and the localization of the sampling points Samples were collected from locations arranged perpendicular to the shore line, using a device type corer, (being withheld evidence in its entirety - sediment and biological material caught), from different horizons of depth (Table 1), after which fixing and conservation were conducted in order to be processed in the laboratory. Table 1: The number of samples which were included in this study and the localization of collecting point Localization of samples collecting point Mediollittoral C. Midia, Constanta, Eforie Sud, Mangalia, Vama Veche Infralittoral: C. Midia, Constanta, Eforie Sud, Mangalia, Vama Veche Transects: Cape Midia – Constanta and Cape Kaliakra Total samples Depth (m) No. samples 0 12 1,3 and 5 45 8, 15 and 25 20 77 Substratum Hard and sedimentary phytal Hard and sedimentary Exclusive rocky Sediments: Sandy silt and muddy Results and Discussions In this study have been identified 54 species for the main types of habitat considered: sedimentary, hard (especially associated to the phytal and zoo-bioderm) and stone; out of this species, Nereidae JOHN. are 17%, Phyllodocelidae LEVIN are19%, 9% Syllidae SAVIG. (45% of which is Aciculata-Palpata group) and 50% of 131 Scolecidae BLAIN (sedentary, with external tubs of sediment, out of which 37% represents Spionidae GRUBE) 7% from other groups; juvenile and larval forms are dominated by spionidae, followed by nereidae. Although the number of samples collected in the Kaliakra area is much lower compared to the rest, polychaets recorded a bigger increase in this sector than in the rest of the coast area (58%, Fig. 2); in addition, species cited only in habitats of these areas represent 62% of the species cited only with a single presence (Fig. 3). Polychaeta- Species number RO 42% BG 58% BG RO 25 m 48% 15 m 52% 15 m 44% 25 m 56% Fig. 2 – Distribution of the number of species identified in the researched area: C. Kaliakra-Bulgarian littoral and the rest of the researched area-Romanian littoral Also in the area C. Kaliakra, in the biotopes from 25 m depth, polychaets recorded the highest number of species identified, relative to the total number cited for the entire area; in the habitats located between C. Midia and Vama Veche were recorded values approximately equal for the number of species recorded on various depth horizons (Fig.2). Constant 23% RO 47% BG 53% One present 62% Frequent 15% Constant: more 80% ; Frequent: more 50% ; Fig. 3. – The analysis of the polychaeta species frequency in the two sectors of the studied area Staying in the same context, data analysis performed for the fauna of benthal metazoars (79 species), presents the northern extremity of the analyzed area (Cape Midia - Constanta) as the area with the greatest number of species and the highest values of density on abundance particularly in the horizon of depth to 15 m 132 (especially by representatives of groups Polychaeta - 27 species and Mollusca - 23 species, Fig. 4). In specific literature it is considered that approximately 75% of the benthic fauna of the Planetary Ocean is encountered in combination with hard substrate (rock, coral reefs, artificial reefs, hydro-technical constructions, or shell-type), 20% is populating sedimentary biotopes and only 5% of the benthic fauna is associated to the phytal substrate (Parsons, 1977). Metazoa (Davg*m-2) 25 m 14% RO 59% BG 41% Density metazoa/deep w ith 32 metazoa species 25 m 53% 15 m 47% w ith 23 metazoa species for each deep interval 15 m 86% w ith 21 metazoa species Fig. 4. - Analysis of the number of species and of the density after the benthic fauna abundance from the two sectors of the studied area For the study area presented shows is highlighted an almost constant presence of nereidae species, with high waist: Neanthes succinate LEUCK., Nereis rava EHLERS., with affinity for hard substrate, frequent in association with epibenthic fauna of this substrate; they are present also in association with various sedimentary deposits and this is correlated with the presence of rocks and stones large enough, at whose shelter can form such accumulation of sediments (Fig. 5); the last species quoted by us as a novelty for the Romanian coast (Paraschiv et.al., 2001); as well as a novelty in the `90 was reported for the first time at the Romanian seacoast a species of nereid, Namanereis litoralis MAR., in the mediollittoral sediments, at shelter from waves and with high concentration in particulate organic matter in interstitial water (Surugiu and Manoleli, 1998; Paraschiv and Gomoiu, 2002); populations of this polychaeta are described in the literature as typical for the mediollittoral with sediments dominated by fine fractions and with increased organic load (Vinogradov, 1968); in the study conducted by us, we found it in high enough number in the fauna associated to the protection breakwaters of the port of Cape Midia. Among the species characteristic to the rocky substrate, with epibenthic consisting in mussels and macroalgae associations, and frequently encountered by us, we quote: Platynereis dumerilii AUDOU.&EDW. and Perinereis cultrifera GRUBE. Among the forms of vagile polychaeta, a fairly large percent of species, especially among syllidae and phyllodocelidae, presents an accentuated affinity to the hard substrate particularities (38%, Fig. 5). 133 80 70 soft substratum hard sustratum F% FD% 60 50 40 30 20 Sp h yd o Po l N ea nt he s su cc in ea ra an ae te ro nn sy at lli a s bu lb Po os ly a do ra ci li a ta N er ei s ra B va ra ni a cl N er av in at e a Pl ci at rr at yn ul er us ei s Pe du ri m ne er re i li is i H cu ar lt r m ife ot ho ra e re tic ul at a 10 0 Sp. Polychaeta species num ber total num ber identificated: 54/2002-2006 16 14 12 10 8 6 4 2 0 sedim 5% until 3 m 4% rocky, until 3 m 9% RkD population from 10-25 m deep population from 3 m deep and rocky substratum A o on ni d e id es s o pa xy c uc e ib pha ra nc l a B h r C C ani iat a ap a a ito pite cl a m l v as la c ata ap t C us i ap m tat a ite in lli imu d Po es s g ly do iar C d Eu lym ra c i ili ch en on e c ata o e ru lla ris br o Et c in ct eo Eu ne a pi la ct F lia a G abr lim ru ic ba ia be t a s a te a b nu el l G a i Po rub cirr a e ly do a l t a ra imb a an te ta nn at a RkD deep biotop 44% everywhere 38% A Sp. Fig. 5 – The structure of the Polychaeta communities from the different types of occupied habitats A relatively large number of species (44%), are identified only in biotopes at depths exceeding 10 m; this is explained mainly by the presence at these depths of a particular type of sediments that form the matrix substrate (silt with slimy matrix) and the preference is given rather by the need to "build" the tube to carry out life-cycle and to a lesser extent by bathymetric factors; among these species we quote: the species of Capitella BLAINV., Capitomastus LANGERH, Polydora BOSK and Aonides CLAP., species Eucymene CLAP. and 134 12 10 8 6 4 2 0 N ea nt h es Po su ly cc do Sp in ra ea ha an er t en os na yl lis ta bu Fa lb br os ic ia a sa be N lla er ei s B ra ra va ni a c Po la va yd Pl ta or at yn a ci er l ia ei ta s du G m ru er be il i a i Po l im yd ba or Pe ta a ri n la rv er .+ ei ju s cu v l tr i fe ra F% 90 80 70 60 50 40 30 20 10 0 Polychaeta fauna from shalow w ater zone (hard and sedim entary substratum ): 28 taxa/2002-2003 Rang (RkD) Heteromastus CLAP. whose population occupies the first positions (after the rank given by the frequency – F% and dominance – DD % values) in the polychaeta fauna communities of the investigated sector (Fig. 5). Mediollittoral floor is characterized on the entire length of the analyzed coastline segment by sedimentary habitat with fine grading (C. Midia, Constanta), average and rough (Eforie Sud) and rough mixed with fragments of shell more or less run (Vama Veche); habitats of the far south, are populated by rare species strictly affinity of sediment habitats: Saccocirrus papillocercus BOBR. (216 indv.m-2) and Nerilla antennata SCHM. (1068 indv.m2 ) (Surugiu, Manoleli, 1998-1999); the most part of the species that have been identified in the biotopes of this floor and that dominate through values of the average density of the populations are the ones associated to the hard substrate epibenthic organisms (Fig. 6): Neanthes succinea (12 378 indv.m-2), Perinereis cultrifera (936 indv.m-2), Platynereis cultrifera (1 097 indv.m-2) and Nereis rava (Nereidae), Brania clavata CLAP.(1 174 indv.m-2) and Sphaerosyllis bulbosa SOUTH. (Syllidae), species of the Polydora genus (3 114 indv.m2 Populations of these species record the first five values of density rank (RkD) because of the frequency and/or increased densities. In the mediollittoral sediments from Eforie South is highlighted increased average density values (438 indv.m-2) recorded by the population of Namanereis litoralis. F% Sp. RkD Fig. 6 – The structure of polychaeta associations from the sediments and rocky substrate of the mediollittoral area, Cape Midia - Vama Veche The sedimentary habitats of the infralittoral are dominated throughout the entire length of the analyzed coastline segment by a lower number of species, but which develops increased effectives, even if they are not recorded consistently; at this level the species of Scolecidae group are dominant (Fig. 7): Nerine cirratulus DELLE-CHIAJE (3 758 indv.m-2), Spio filicornis O.F.M. (1 418 indv.m-2), Polydora ciliata JOHN. (1 087 indv.m-2); the Neanthes nereid population is reported especially in areas with development mussels effectives, but with much lower values (650 indv.m-2). 135 at N er in e Rang (RkD) Sp io ci rr fi l ic or ni Et s eo ne Sp pi io ct ni a da e la N rv er ae in id ae la Po rv ae ly do ra Po ci ly lia do ta Sp ra ha la er rv .J os uv yl lis N b ea ul bo nt he sa s su cc in ea 10 9 8 7 6 5 4 3 2 1 0 ul us F% Polychaeta fauna from sedim entary substratum : 24 taxa/2003-2005 100.00 90.00 80.00 70.00 60.00 50.00 40.00 30.00 20.00 10.00 0.00 Sp. 10 9 8 7 6 5 4 3 2 1 0 Rang (RkD) Polychaeta fauna from hard substratum : 36 taxa/2003-2005 in ea Po yd or a Sp sp N . ha er e er is os ra yl va lis Po b ly u do lb os ra H a ar an m t en ot na ho ta e Pe re ri n tic er ul ei at s a Pl cu at yn l tr i fe er ei ra s du m B er ra il i H ni i ar a m c la ot va ho ta e im br ic at a 100.00 90.00 80.00 70.00 60.00 50.00 40.00 30.00 20.00 10.00 0.00 RkD N ea nt h es su cc F% F% Sp. F% RkD Fig. 7 – The structure of the polychaeta associations from the sediments and rocky substrate of the infralittoral (until 25 m), Cape Midia – Cape Kaliakra The hard substrate infralittoral is characterized by the fact that the frequency index values are very close to a relatively large number of species (Fig. 7), though dominant through effectives are only two populations of the Polydora (Polydora sp. 32 017 indv.m-2 and P. antennata 15 034 indv.m-2); at a significant difference (6511 indv.m-2) is encountered the population of the Neanthes (RkD 3) and species Sphaerosyllis (RkD 4; 4029 indv.m2 ). While with lower effectives, we report the presence of populations of certain genus from Phyllodocelidae group: genus Harmothoe KINBERG. (H. reticulata CLAP. and H. imbricata L., on average 1400 indv.m-2), Polynoe scolopendrina SAVIG. (1250 indv.m-2), Eteone picta QUATR., Eulalia limbata CLAP. and E. viridis MULLER (on average 740 indv.m-2), Euchone rubrocincta SARS (65 indv.m-2). Analyzing from the feeding stand point the associations formed by polychaeta-fauna, two main groups are highlighted: the predators - 33% (in this group being included non-selective carnivores) and the detritivore species - 29% (consuming particulate organic substance, indifferent of the mechanisms used, Fig. 8). 136 polyvalent troph. 20% Trophic stucture of polychaeta community predatory 33% sedimentphag 18% detrivorous 29% Substr. soft Substr. hard 20 Substr. soft Substr. hard 15 No.sp. No.sp. 20 15 10 5 0 10 5 0 0-3 m until 10m until 25 m Depth 0-3 m until 10m Depth until 25 m Fig. 8 – Trophic structure of polychaeta communities from different habitats types The group of predator species includes the syllidae (Sphaerosyllis bulbosa, Syllis gracilis GRUBE, Brania clavata, Grubea limbata CLAP.and G. tenuicirrata MAR.), Harmothoe şi Phyllodoce SAVIG. species from genus. Some nereidae species are included in the non-selective carnivores group because they present a multiple trophic valence recognized in the literature (eg Hediste diversicolor O.F.M.). The largest number of species in this group was identified in the hard substrate habitats associated to the infralittoral floor (Fig. 8). The second group which includes a relatively large number of species is the on of detritivorous species; in this largest group are included the species of spionidae, scolecidae and terebelidae (Canalipalpata): the species of genus Aonides CLAP, Polydora, Spio FABR., Nerine, Euclymene CLAP., Heteromastus CLAP, Capitelida, and some nereidae – Namanereis litoralis. Out of these species are highlighed selective micro- or macrodetritivorous, as well as non-selective species. Conclusions The variety of the biotopes encountered in the littoral sector Cape Midia - Cape Kaliakra (between 0 and 25 m deep) is the premise of their employment by a diverse fauna; there are are encountered sedimentary habitats with mixture variants of the clay, silt and sandy fractions (the last category with grading subdivisions of fine, medium and rough sand, mineral or biogenic – shells material, rough, strongly run), as well as habitats characterized by a hard substrate (limestone platforms more or less extensive in the southern extremity of the area investigated, the protection breakwaters for the beaches and of the harbor from C. Midia to Mangalia, or substrate composed of strongly compacted shell material). On the basis of the 77 benthos samples collected from the C. Midia - C. Kaliakra sector, there were identified a total of 199 specific and supraspecific taxa: 117 taxa of 14 major groups of metazoars identified in the small depth benthal domain, to the north of Mangalia (with more sedimentary habitats) and 82 taxa of 18 major groups, for the Vama Veche - Cap Kaliakra sector; this situation is due to rather low number of samples collected from this sector than to the lower diversity (this not allowing the identification of a greater segment benthos fauna typical to the hard substrate). However we mention the presence of a greater number of species in the group Polychaeta (Annelida) in the southern extremity of the investigated littoral sector (58% of the total number of polychaeta species - 54) compared with 42% recorded in the benthos domain of north of Mangalia; this is explained by the greater variety of categories of sedimentary habitats or with hard substrate in the area. A constant presence (presence in percents of more than 90%) in almost all types of habitat is registered nearly 23% of Polychaeta species (Nerine cirratulus, Polydora species complex, Capitella capitata FABR., Sphaerosyllis bulbosa, etc); a high enough percentage (62%) is represented by the category of species cited as unique presence in one habitat or another, in a 137 coastal area or another; from this fauna segment, 18 fauna species are cited as unique presence for the habitats from the south of Vama Veche (hard substrate: Microspio mecznikowianus CLAP., Janua pagenstecheri QUATRE, or at more than 15 m depth). We signalize the presence of the populations of some polychaeta species cited by us in previous works as new presence for areas situated to the south of Odessa Bay: Nereis rava and Namanereis litoralis; if approximately 10 years ago we were reporting in the mediollittoral from Eforie South the presence of Namanereis species population, at present we can say that it is present as well in the sedimentary deposits sheltered at the base of the brakewaters from Cape Midia (even if not in increased effectives, 487 indv.m-2). Mediollittoral sedimentary habitats from Cape Midia to Constanta, are characterized by an extremely poor polychaeta fauna, consisting of more juvenile and larval stages of spionidae; as one goes further to the south, the sediments granulometry of this is changing, the rough fractions becoming dominant (Eforie Sud, Mangalia); in these habitats, considered in the `70 as being populated by the association of Ophelia bicornis polychaeta species (now disappeared from these habitats) we believe that restructuring of the invertebrate communities take place; deposits of small fragments, of bivalves shells (especially mussels) from the mediollittoral from Vama Veche, exposed to wave action, are populated mainly by two typical interstitial species: Saccocirrus papillocercus and Nerilla antenna; since in the literature Nerilla antenna is described as a typical small depth and psammophyl species and we have identified the representatives of this species and in association with phytofil fauna, as well as in habitats from sandy depths greater than 30m, we believe that it could be in this case a species complex, too. The mediollittoral with rocky substrate and epibenthos is dominated by nereidae species: Neanthes succinea, Perinereis cultrifera, Platynereis dumerilii, Nereis rava. The infralittoral with sediments is populated mostly by species of Polydora complex, by Nerine cirratulus, Spio filicornis, Pygospio elegans CLAP., Prionospio cirrifera WIREN; to a high enough extent, to the northern area investigated, capitelidae species develop populations with relative great effectives: Capitella capitata, Capitella minima LANGER., Capitelides giardi MESNIL, and the species Euclymene collaris, Heteromastus filiformis. In the infralittoral areas with hard substrate (particularly to the south of the area investigated), where are commonly encountered mussels colonies, associated to this particular type of habitat are encountered to a higher extent species of syllidae, phyllodocelidae, vagile forms, and mostly predators. Under feeding aspect, the polychaeta communities in the area studied are grouped into four major groups: predators (ravening and non-selective, Syllidae, Harmothoe, Polynoe SAVIG.), detritivorous (macrophagous and micophagous), the majority of scolecidae group), sedimentophagous (most of capelidae species) and the group of the species with a polyvalent trophic regime (the majority of nereidae species). References 1. 2. 3. 4. 5. 6. 7. BARTOLOMAEUS T., Purschke, G., Hausen, H., 2005 – Polychaete phylogeny based on morphological data – a comparasion of current attempts; Hydrobiologia 535: 341-356. B CESCU M.C., 1972 – Substratum; Marine Ecology, vol. 3, part 3; 1291-1314. BELLOT A., BRUNETTI, R., BURATTO, A., GABRIELE, M., GALLOTTI, D., MASIERO, L., 2004 – Community structure and abundence of sublittoral meiobenthos of Nortern Adriatic Sea; Bollettino del Museo Civico di Storia Naturale di Venezia, 55: 53-65. GLASBY J. C., 1999 – The Namanereididae (Polychaeta: Nereididae). Part 2, Cladistic Biogeography; Records of the Australian Museum, Supplement 25: 131-144. GLASBY J. C., 2005 – Polychaetae distribution patterns revisited: an historical explanation; Mar. Ecology 26: 235-245. GOMOIU, M.T. - 1981 – Some problems concerning actual ecological changes in the Black Sea; Crecet ri Marine, IRCM-Constan a, 14:109-127. KISSELEVA M. I., 1968 – Le développement du benthos dans les mers du bassin méditerranéen; Rapp. Comm. Int. Mer Medit., 19, 2: 103-105. 138 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. ***, 1985 – Vidovoi sostav i colicestvennoe razvitie razlicinâh razmernâh gruppirovoc bentosa v necatorâh soobşestah Cernogo Morea; kologhia morea, B 21: 15-19. MUSCO L., Giangrande, Adriana, 2005 – Mediterranean Syllidae (Annelida-Polychaeta) revisited: biogeography, diversity and species fidelity to environmental feature; MEPS 304: 143-153. PARASCHIV G. M., GOMOIU, M.T., 2002 – New species of Cnidaria in the Black Sea: Halammohydra sp. and Stylocoronella sp., interstitial forms at mid-littoral sandy beaches; Proc. Intern. Workshop on “Modern and Ancient Environments and Processes”- Geo-Eco-Marina 5-6/2000-2001 Bucureşti: 53-58. PARASCHIV G. M., 2006 – Present state of Polychaeta worms populations in the NW Black Sea; 1st biannual Scientific Conference Black Sea b.Ecosystem 2005 and Beyond-commision on the Protection of the Black Sea Against Pollution, 8-10 May 2006, Istanbul-Turkey: 566-579. PARASCHIV, G. M., GOMOIU, M.T., ŞERBAN V., 2001 – New species of Polychaeta (Annelida) from the Romanian Black Sea coast; 3rd International Conference of PhD Students, 13-19 August 2001, University of Miskolc, Hungary: 271-278. PARSONS T. R., TAKAHASARI, M., HARGRAVE, B., 1977 – Biological Oceanographic Processes. Pergamon Press Ltd. Headington Hill Hall, 280 pp. SERGHEVA V., ZAIKA, M., KISSELEVA, M., 1998 - Two polychaeta species bordering deep sea anoxic water in the Black Sea; Tavrichesky med.-biolog., Vestnik, no.1-2: 56-60. SKOLKA M., F G RAŞ, M., PARASCHIV, G. M., 2005 – Biodiversitatea Dobrogei, 132-134, (ed) Ovidius University Press, Constan a. SURUGIU, V., MANOLELI, D., 1998-`99 – Nouvelle contribution á l`etude des Annélides Polychétes de la region d`Agigea (Littoral Roumain); An. Stiin. Univ. “A.I. Cuza”, Iaşi, Biol. Animal , fas. XLIVXLV. VINOGRADOV K. A., LOSOVSKAYA, G. V., 1968 – Klass mnogoshetinkovye chervil – Polychaeta/ Opredelitel`Fauny Cenogo I Azovskogo Morey; Naukova Dumka I, Kiev: 251-359 pp. 139 NATURA 2000 EUROPEAN ECOLOGICAL NETWORK IN ROMANIA Loreley Dana JIANU *, Silvia Raluca TURCU* Constanţa Environmental Protection Agency, Unirii Street, No. 23, 900532, Constanţa, Romania jloreley@yahoo.com _________________________________________________________________________________________ Abstract: Natura 2000 is a Community-wide network of nature protection areas established under the 1992 Habitats Directive. It also includes areas designated under the 1979 Birds Directive. Aim of the network is long-term survival of Europe's most valuable and threatened species and habitats. Natura 2000 is not a system of strict nature reserves where all human activities are excluded. Keywords: Natura 2000, Habitats Directive, Birds Directive, environmental assesment, Constanta County’s sites __________________________________________________________________________________________ Introduction European ecological network Natura 2000 is a network of protected natural areas, through implementation of European Directives 92/43/EEC - Directive on the conservation of natural habitats and species of plants and wild animals (Habitats Directive) and 79/409/EEC - Directive on the conservation of wild birds (Birds Directive). The term Natura 2000 comes from the Habitats Directive and symbolizes efforts to conserve biodiversity for the year 2000 and in the future. Discussions Protected areas Natura 2000 are of two types: Special Areas of Conservation - SAC-s, designated under the Habitats Directive and Special Protected Areas for Birds - SPA-s established under the Birds Directive. The establishment of this network of protected areas where special measures are taken to conserve biological diversity also fulfils a clear Community obligation under the UN Convention on Biological Diversity. Nature 2000 sites selection in Romania follows two different selection processes. First, the identification and delimitation of SPA-s is entirely based on scientific criteria, and than declared as Natura 2000 sites. Second process concerns SAC-s selection, and follows few steps. Once the national list of Sites of Community Importance (SCI-s) have been adopted it is then for the Romanian State to designate these sites as SAC-s as soon as possible and within six years at most (complying by Habitats Directive criteria in the Biogeographyc Seminars debates). During this period the state should establish the necessary management or restoration measures for the sites to ensure their favourable conservation status (FCS). The first FCS monitoring report will be in 2013 for the SCI-s declared in Romania. The purpose of Natura 2000 network is to stem the decline of biological diversity by maintaining or restoring favorable conservation status of species with different degrees of endangerment (rare, vulnerable or endangered) and natural habitats of European interest. The conservation status are favorable when the species is maintained in the long term, not the natural habitats aren’t reduced are also are sufficiently broad to maintain populations in the long term. In the same time, Natura 2000 network is the main instrument of the European Union for the Conservation of biodiversity and nature, it’s irreversible loss means to affect the production of goods and services and semi-natural ecosystems, and economic well-being and health of human populations. European ecological network objectives are identifying, maintaining and restoring key areas to protect species of wild fauna and flora, and corridors linking of these, which make it possible migration and exchange between the peoples populating the same species as habitats of different areas. Romania is characterized by: the presence of five biogeographical regions (Pannonian, Steppic, Alpine, Continental and Pontic or the Black Sea region) due to geographical position - being the only country in Europe 140 with five biogeographical regions, the diversity of hydro-geomorphological units, maintaining a share of approximately 45% of natural ecological systems or partly natural from total area of the country and maintaining most types of systems and complex natural ecological systems. Both European Directives 92/43/EEC and 79/409/EEC have been translated into Romanian legislation by several legislative acts, namely: Emergency Ordinance no. 57/2007, with subsequent amendments on the regime of protected natural areas, conservation of natural habitats, wild flora and fauna, Order of the Ministry of Environment and Sustainable Development no. 1964/2007 declaring sites of community importance as part of European ecological network Natura 2000 in Romania and the Government Decision no. 1284/2007 declaring special protected areas for birds as part of European ecological network Natura 2000 in Romania. Specific lows in Romania (Emergency Ordinance no. 57/2007; Order of the Ministry of Environment and Sustainable Development no. 1964/2007, Government Decision no. 1284/2007) provides for all the plans, programmes and projects to be carried out in the Natura 2000 sites and close to them the obligation of applying the procedure of making environmental assessment for plans and programs and procedure framework for environmental impact assessment for projects. Thus, not any type of human activity is a priori prohibited in Natura 2000 sites or in the vecinity, the situations are distinct from case to case and evaluate differentiated. Projects and plans to be achieved, however, are of major public concern, including the sake of social or economic order. For this development proposals competent authority for environmental protection will determine and establish the compensatory measurements necessary to protect the coherence of the Natura 2000 network. In our country are designated 108 areas of special protection for birds (SPA-s), meaning approximately 12% of the area of national territory and 273 sites of Community importance (SCI-s), which means approximately 13% of the area of the country. In the county of Constanta are 20 SCI-s (Fig. 1) and 22 SPA-s (Fig. 2) declared to protect a significant number of very diverse habitats (forest, meadow, coastal, swamp, rocks, sand) and a number of important species of flora and fauna of Community interest. Fig. 1 Limits of sites of Community importance (SCI-s) within the county of Constanta 141 Fig. 2 Limits of areas of special protection for birds (SPA-s) on the county of Constanta The 20 sites of Community Importance present wholly or partly within the county of Constanta are the following: 1. ROSCI0006 Balta Mic a Br ilei 2. ROSCI0012 Braţul M cin 3. ROSCI0022 Canaralele Dun rii 4. ROSCI0053 Dealul Alah Bair 5. ROSCI0065 Delta Dun rii 6. ROSCI0066 Delta Dun rii - zona marin 7. ROSCI0071 Dumbr veni - Valea Urluia - Lacul Vederoasa 8. ROSCI0073 Dunele marine de la Agigea 9. ROSCI0083 Fântâniţa Murfatlar 10. ROSCI0094 Izvoarele sulfuroase submarine de la Mangalia 11. ROSCI0114 Mlaştina Hergheliei - Obanul Mare şi Peştera Movilei 12. ROSCI0149 P durea Esechioi - Lacul Bugeac 13. ROSCI0157 P durea Hagieni - Cotul V ii 14. ROSCI0172 P durea şi Valea Canaraua Fetii - Iortmac 15. ROSCI0191 Peştera Limanu 16. ROSCI0197 Plaja submers Eforie Nord - Eforie Sud 17. ROSCI0201 Podişul Nord Dobrogean 18. ROSCI0215 Recifii Jurasici Cheia 19. ROSCI0269 Vama Veche - 2 Mai 20.ROSCI0273 Zona marin de la Capul Tuzla. The list of specially protected areas for birds on the county of Constanta includes the following sites: 1. ROSPA0001 Aliman – Adamclisi 2. ROSPA0002 Allah Bair – Capidava 3. ROSPA0005 Balta Mic a Br ilei 4. ROSPA0007 Balta Vederoasa 5. ROSPA0008 B neasa - Canaraua Fetei 6. ROSPA0017 Canaralele de la Hârşova 7. ROSPA0019 Cheile Dobrogei 8. ROSPA0031 Delta Dun rii şi Complexul Razim – Sinoie 9. ROSPA0036 Dumbr veni 142 10. ROSPA0039 Dun re – Ostroave 11. ROSPA0040 Dun rea Veche - Braţul M cin 12. ROSPA0053 Lacul Bugeac 13. ROSPA0054 Lacul Dun reni 14. ROSPA0056 Lacul Oltina 15. ROSPA0057 Lacul Siutghiol 16. ROSPA0060 Lacurile Taşaul – Corbu 17. ROSPA0061 Lacul Techirghiol 18. ROSPA0066 Limanu – Herghelia 19. ROSPA0076 Marea Neagr 20. ROSPA0094 P durea Hagieni 21. ROSPA0100 Stepa Casimcea 22. ROSPA0101 Stepa Saraiu – Horea. Whereas the Natura 2000 network certainly includes nature reserves most of the land is likely to continue to be privately owned and the emphasis will be on ensuring that future management is sustainable, ecologically, economically and socially. We make the mention that in Constanta County all the natural reserves are included in Natura 2000 sites, thus their protection status is consolidated. References 1. 2. 3. 4. 5. 6. 7. 8. www.mmediu.ro www.anpm.ro www.mediu-constanta.ro/ http//ec.europa.eu/environment/nature/legislation/ habitatsdirective/ http://ec.europa.eu/environment/nature/legislation/ birdsdirective/ Emergency Ordinance no. 57/2007, with subsequent amendments on the regime of protected natural areas, conservation of natural habitats, wild flora and fauna Order of the Ministry of Environment and Sustainable Development no. 1964/2007 declaring sites of community importance as part of European ecological network Natura 2000 in Romania Government Decision no. 1284/2007 declaring special protected areas for birds as part of European ecological network Natura 2000 in Romania 143 FORMULATION OF A SHORELINE DEVELOPMENT INDEX TO EXAMINE THE RELATIONSHIP BETWEEN DEVELOPMENT AND ECOLOGICAL INTEGRITY Lucica TOFAN*, Timothy J. EHLINGER**, Megan HELT-BALDWIN**, Diana CERJAK**, Daniela VASILE*, Richard SHAKER*, Mirela BUCUR*, and Ana Maria BUICULESCU* * Ovidius Universiy of Constanţa, Natural and Agricultural Sciences Faculty 124, Mamaia Bd., Constanţa, 900527, Romania ** University of Wisconsin, Milwaukee, USA __________________________________________________________________________________________ Abstract: This paper presents a rapid methodology that was created for the assessment of shoreline development around an urban lake. Human activity on the land affects the functionality of different areas of the lakeshore. This multi-metric index attempts to collect information to examine the interconnectivity of aquatic, shoreline, riparian, biotic, and viewscape variables at sites along Lake Tabacarie, Constanta Romania. The aquatic, shoreline, and riparian variables were observed by using a modified point-transect methodology following the lake shoreline. Vegetation, organic debris, garbage, ground cover, and land usage were assessed at each sample point around the lake perimeter. The biotic variables were assessed by observation of presence of birds, amphibians, and other fauna at each site. Viewscape was evaluated using a qualitative assessment of natural landscape and culturally important or aesthetically pleasing built environs as compared to impervious surface areas (e.g. parking lots), degraded building, or commercial areas directly on the shore. Data collected were processed into a point scale and scores were given to 98 locations around Lake Tabacarie. The scores created by the application of this methodology can be utilized as indicators of the integrated environmental health and human activity. Furthermore, it can help inform and monitor sustainable development around Lake Tabacarie. Keywords: sustainable development, Tabacarie lake, functional zones, shoreline development index; __________________________________________________________________________________________ Introduction An interdisciplinary study was undertaken to develop a framework for integrated sustainable development for the Lake Tabacarie area, Constatana Romania. The first step of this study was to define the spatial characteristics of the built and natural environmental features, in an attempt to define “functional zones” that could serve as a basis for creating a systems-based model for studies of social, environmental, and economic factors. Based upon examination of satellite orthophotos, the area around the lake was divided into different land cover zones and the human activities within these zones were described (Figure 1). This formed the basis for eleven “functional zones”, including the (1) Holiday Village, Luna Park, and Shops, (2) Tabacarie Park and Playground, (3) City Park Mall, (4) Activity Park, (5) St. Mina Church Area, (6) Micro Delta Reserve, (7) The Natural Science Park, (8) Open Green Space, (9) Commercial Area, (10) North Water Treatment Plant, and (11) Arena and North Green Space. Human actions on land affect the shoreline, which in turn affects the aquatic zone. This is an issue of connectivity. Connectivity assumes the union of smaller parts. The functional zones are connected by the Lake T b c rie shoreline. The purpose of the study described in this paper is to develop a multi-metric index to gather the data needed to quantify and understand the relationships between human activities on the shoreline and the ecological integrity of the lake. This shoreline index provides a methodology to rapidly assess components of the 144 ecological integrity along the shoreline and visualize the spatial relationships as part of indentifying and monitoring sustainable development opportunities. Material and Methods A visual survey was conducted to gather information for 98 locations around Tabacarie Lake. At each location, data were evaluated for an area 10m by 10m square at each survey point. Five components of the Shoreline Development Index were considered: the Aquatic Zone, the Shoreline Zone, the Riparian Zone, a Biotic Component, and an Aesthetic Component. For each sampling point, a transect depth of 5m into the aquatic zone and 10 m into the riparian zone, with a 1m depth from the water edge for shoreline was used at each location. For the aquatic zone, shoreline, and riparian zone, the percent coverage of different vegetation, ground cover and land uses were estimated visually (see example data sheet in Figure 2). 145 The presence of birds, amphibians, and other fauna at each site were noted as either absent, present or many. Aesthetic value was determined by a qualitative assessment of natural landscape and culturally important or aesthetically pleasing built environs visible from the site. The surveys also took note of pollution sources, canopy cover, public vs. private ownership, and the “buffer zone” between lake and manmade surface. It should be noted that surveys were meant to be a rapid assessment of the locations. One person took consistent notes and filled out the surveys. Pictures of each location were taken from the shore facing land and from the land facing water. GPS was used to accurately identify locations. Aquatic Component Data were entered into Microsoft Excel ™, and the statistical distributions of the different variables were examined. Variables that were considered to contribute positively to ecological integrity were assigned positive scores and summed to generatate a “good” score. Variables those that were considered to subtract from ecological integrity were given negative scores and summed to create a “bad” score. The presence of vegetation was considered as something that added value to the aquatic zone. The types of vegetation that were present included, reeds, sedges, submerged and floating vegetation. The aquatic good score was determined by adding percent of reeds, sedges, submerged vegetation and floating vegetation, and was given the variable name “AqGoodScr”. Equation 1 shows how the variables where added: Equation 1: AqGoodScr = PercReed + PercSedge + PercSubVeg + PercFloatVeg, where AqGoodScr = good score for the aquatic component, PercReed = percent of reed, PercSedge = percent of sedge, PercSubVeg = percent of submerged vegetation, PercFloatVeg = percent of floating vegetation. Based upon the total AqGoodScr, a point value between 0 and 15 was assigned. Table 1 shows the scores once all the good variables were added and the point values that were given to each range of scores. The variables that were considered good received the highest scores. Table 1: Aquatic Good Scores AqGoodScr (Total) 0-5 5-20 20-40 40-60 60-80 80-100 Points Given 0 3 6 9 12 15 Negative variables were determined to be the categories of percent litter and percent other. The percent other category usually consisted of algae and brown foam and thus was determined to be a negative variable. The equation given to the bad score of the aquatic zone was named “AqBadScore.” Equation 2 shows how the variables were added. Equation 2: AqBadScr = PercLitter + PercOther, where 146 AqBadScr = aquatic bad score, PercLitter = percent of litter, PercOther = percent of other. Table 2 shows the scores once all the bad variables were added and the point values that were given for each range of scores. Low scores were given the most points as they signified the absence of bad variables. Table 2: Aquatic Bad Scores AqBadScr (total) 0-5 5-20 20-40 40-100 Points Given 5 3 2 0 Once the points were given for each site, the total aquatic score was found at each site. Equation 3 represents the total equation score. The most points a site could have were 20 points. Equation 3: AqTOTscr = AqGoodScr + AqBadScr, where AqTOTscr = aquatic total score, AqGoodScr = aquatic good score, AgBadScr = aquatic bad score. Shoreline Component After all of the data was inputted into excel, each of the different variables was assessed as a positive or negative aspect of the shoreline. The percentage of reeds, sedges, grass, and trees were determined to be positive, or “good” variables, and were added up as the “SLGoodScr”: Equation 4: SLGoodScore = %reed + %sedge + %grass + %tree, where SLGoodScore – good score for shoreline component. Table 3 shows the scores once all the good variables were added and the point values that were given to each range of scores. The variables that were considered good received the highest scores, and those who did not scored good, were given the lower scores. Table 3: Shoreline Good Scores Added Good Scores Points Given 0-10 0 10-20 2 20-40 4 40-60 6 60-80 8 80-100 10 The percentage of litter, wall and rock on the shoreline was determined to be negative or “bad” variables and were added up as the “SLBadScr”: 147 Equation 5: SLBadScore = %Litter + %Wall + %Rock, where SLBadScore = bad score for shoreline component. Table 4 shows the scores once all the bad variables were added and the point values that were given to each range of scores. Absence of bad variables was given the highest scores. Table 4: Shoreline Bad Scores SLBadScore 0-10 10-20 20-40 40-100 Points Given 10 5 3 0 The total shoreline score was then decided by adding the points given for the good score and the points given for the bad score. The highest points given could add up to 20. Equation 6 shows the total shoreline score: Equation 6: SLTOTScr = SLGoodScr + SLBadScr, where SLTOTScr – total score for shoreline component, SLGoodScr – good score for shoreline component, SLBadScr – bad score for shoreline component. Riparian component Within the riparian zone, positive variables included percent grass, reed, sedge and shrubs or trees. Equation 7 shows the equation that was used to determine the “RipGoodScr” Equation 7: RipGoodScr = PercReed + PercSedge + PercShrbTree + PercGrass, where RipGoodScr = good score for riparian, PercReed = percent of reed, PercSedge = percent of sedge, PercShrbTree = percent of shrubs and trees, PercGrass = percent of grass. Table 5 shows the scores once all the good variables were added and the point values that were given to each range of scores. The variables that scored good received the highest scores. Table 5: Riparian Good Scores RipGoodScr (total) 0-10 10-20 20-40 40-60 60-80 80-100 Points Given 0 2 4 6 8 10 148 Negative variables were determined as percent concrete, bare soil, and other. The other variable was usually found to be litter. Equation 8 shows the equation that was used to find the “RipBadScr.” Equation 8: RipBadScr = PercConcrete + PercBareSoil + PercOther, where RipBadScr = bad sore for riparian component, PercConcrete = percent of concrete, PercBareSoil = percent of bare soil, PercOthere = percent of others. Table 6 shows the scores once all the bad variables were added and the point values that were given for each range of scores. Low scores were given the most points as they signified the absence of bad variables. Table 6: Riparian bad scores RipBadScr (total) 0-10 10-20 20-40 40-100 Points Given 10 5 3 0 The final score for each site was decided by adding the RipGoodScr and RipBadScr variables. The highest score for each site was 20. Equation 8: RipTOTScr = RipGoodScr + RipBadScr, where RipTOTScr = total score for riparian, RipGoodScr = good score for riparian, RipBadScr = bad score for riparian. Biotic Component The biotic aspect was broken down into two parts. One variable was created for the presence of frogs and another was created for the presence of birds. Both scores had a total of ten points and then could be added to equal 20 total points. Frogs were divided into difference categories. They were either “none”, “present” or “many” at a site. Table 7 shows how the points were determined for the presence of frogs. Table 7: Presence of frogs Presence of Frogs None Present Many Points Given 0 5 10 Presence of birds was done in the same way. Birds were either determined to be “none”, “present” or “many” at a site. Table 8 shows how the points were determined for the presence of birds. 149 Table 8: Presence of birds Presence of Birds None Present Many Points Given 0 5 10 At each site then the presence of frogs was added with the presence of birds. For each site the highest score could be 20 points. Equation 9 shows how this was done. Equation 9: BioScr = Frogs + Birds, where BioScr = score for the biotic component, Frogs = presence of frogs, Birds = presence of birds. Aesthetic Quality Component The aesthetic quality section was broken down into three sections of what could be seen in the viewscape. These sections included natural beauty, aesthetically pleasing built areas, and aesthetically unpleasing built areas. The natural viewscape was given a total of ten points. Likewise, the aesthetically pleasing built areas were also given a total of ten points. The unpleasing built areas had a total of five points that could be taken away from the total score. Once each of these scores was determined in each function zone the scores were added or subtracted. Equation 10 was used to determine the final aesthetic score. Equation 10: AestScr = Natural + PleasingBuilt – UnpleasingBuilt, where AestScr = score for the aesthetic component, Natural = presence of natural features, PleasingBuilt = pleasing built environment, UnpleasingBuilt = unpleasing built environment. This equation was then used to give each functional zone a score based on the view that could be seen within that zone. Total Score At Each Site After all five of the components were assessed and given points, they were then added together to make an overall score at each site. Equation 11 shows everything that was added to make the final overall score. Equation 11: TotalSDIScr = AqTOTScr + SLTOTScr + RipTotScr + BioScr + AestScr, where TotalSDIScr = total Shoreline Development Index score, AqTOTScr = total score for the aquatic component, SLTOTScr = total score for the shoreline component, RipTotScr = total score for the riparian component, BioScr = total score for the biotic component, AestScr = total score for the aesthetic component. 150 Table 9: Total SDI Score Total SDI Score 0-20 20-40 40-60 60-80 80-100 Value Poor Average Good Very Good Excellent Each of the five components was added to make up the total score at each site. Table 9 shows how the scores were then interpreted. Results and Discussions The index results show the connectivity of the riparian zone to the shoreline zone, to the actual aquatic zone. Human activity and its effect on the lake can be quantified, and relations can be understood. Connectivity assumes the union of smaller parts. The smaller parts in this case are the functional use zones around the lake. The functional zones with all of their different uses have the lake as their common connection. When the scores were given to 98 locations around Lake Tabacarie and the Microdelta at the Dolphinarium the results showed most sites to be average, followed by a high amount of poor scoring sites (Fig 3 and 4). Excellent and very good sites were found at the Microdelta and the bay in Tabacarie Park. The high occurrence of reeds along the shoreline and in the aquatic zones in these areas correlated with higher amounts of fauna. Shoreline comprised of concrete wall was an occurrence at a great number of sites and affected the scores negatively. The Bay and the Microdelta from the Dolphinarium scored excellent, while most of the sites varied between poor and average. The Microdelta at the Delphinarium scored “very good” and has the potential to be a model for the revitalization of aquatic, shoreline, and riparian zones on Lake Tabacarie. Fig. 3 Total Shoreline Development Index Scores 151 Fig. 4: Distribution of Shoreline Scores around Tabacarie Lake Amphibian and avian numbers were highest in the Microdelta and a correlation was found between their numbers and a heavily vegetated shoreline. The zone that scored “excellent” the most was the Bay in Tabacarie Park. Generally high percentages of reed and vegetation with low levels of built environment generated an example of a potentially healthy area of the lake system. Conclusions There is a growing need to monitor and evaluate the impacts of development on lake ecosystems (Roan et al 2006, Jennings et al 2003) and to develop indicators that include biotic and abiotic aspects related to sustainable development in and around coastal zones (Butler and deMaynadier 2008, Jackson 2002). It is the interaction among the physical and biological components that contributes to the healthy functioning of ecosystems impacted by human activity. The index presented in this paper provides a rapid method for characterizing the physical and biological features of the shorelines of urban lakes that are related to sustainable development. The impacts of development in the Tabacarie Lake system are growing rapidly. As such, the need to identify areas for preservation and restoration is great. The index presented here can serve as a method for both monitoring impacts and for planning future developments to improve the functioning of the lake system. References 1. 2. 3. 4. BUTLER, R. G., MAYNADIER, P. G., 2008. The significance of littoral and shoreline habitat integrity to the conservation of lacustrine damselflies (Odonata), Journal of Insect Conservation 12(1): 23-36. JACKSON, M.W., 2002. Development of Shoreline Degradation Index (SDI): monitoring environmental change using landscapte ecology metrics and high resolution remotely sensed imagery. Geoscience and Remote Sensing Symposium, 2002. IEEE International, 5(2005): 2844-2846. JENNINGS, M. J.,. EMMONS E. E. et al., 2003. Is littoral habitat affected by residential development and land use in watersheds of Wisconsin lakes?, Lake and Reservoir Management 19(3): 272-279. ROWAN, J. S., CARWARDINE J. et al., 2006 . Development of a technique for Lake habitat survey (LHS) with applications for the European Union Water Framework Directive, Aquatic ConservationMarine and Freshwater Ecosystems 16(6): 637-657. 152 FIVE YEARS OF ACTIVITY CONCERNING THE EDUCATION OF THE COASTAL LANDS PROTECTION Monica AXINI*,** , Rodica BERCU*, Ligia D. DIMA*** * Faculty of Natural Sciences and Agricultural Sciences,”Ovidius” University of Constantza,124 Mamaia Bd 900590, Constantza, Romania ** ”Monachus” Group of Research and Ecological Education, 8 Hortensiei Alley, 900518, Constantza, Romania, monicaaxini@yahoo.com *** Museal Complex of Natural Sciences, 255 Mamaia Bd, Constantza,Romania __________________________________________________________________________________________ Abstract: The coastal lands constitute an ecological balance of the actions and retroactions from flora, fauna and climate. For this reason, it is imperative their sensible conservation and capitalisation. Its constitute the living environment for numerous animals and plants species. But, always, the man has intervened in their balance with the negativest results. In conservation preoccupation of coastal ecosystems, its frames the theoretical and practical activities carried on in the line of pupils by G.C.E.E.M. during 2003 – 2008, two. The major purpose was the development of conscience of young generation concerning the importants of the coastal lands in sustenable maintenance. The present paper point events went by the time of the Wetlands World Day, of the Water World Day, of the Earth Day, of the Black Sea International Day and of during the springs and the summers. Keywords: pupils, ecological education, coastal lands __________________________________________________________________________________________ Introduction The projects adressed to pre – school children, middle school pupils (with age between 11 – 14 years) and high school pupils (with age between 15 – 18 years) and students, too. The purposes of projects was the development of concience of childrens concerning the protection and conservation of coastal lands through: a) the pupils verification concerning their knowledges about coastal lands; b) the delivering of conferences; c) the lectured on coastal lands; d) the maked of trips in various coastal lands from Constantza County; d) the carrying on by pictures, drawings and grapfic arts competitions; e) the drawing up, the printing and the distribution of instructive teaching aids; f) the seeing of documentary films; h) the acting of sketchs (Corneanu et al. 2005). Results and Discussions The pupils verification. The pupils answers showed that they owned some knowledge about nature. But, they wish to know more about that and they will mixed up in projects concerning the knowledge, the protection and the rehabilitating of it (figure 1). 153 Fig. 1 - The pupils verification The delivering of conferences. The participation in great number of pupils at conferences organized for they it showed their interest in theoretical and practical problems of nature in general and specially of coastal zone. The lectures were maked by specialists and pupils. The pupils papers showed that they major preoccupations are: the dolphins of Black Sea, the effects os pollution and the erosion of coastal zones, the algae from romanian littoral of Black Sea and their importance in human food, legislation, the history of scientific researchs concerning coastal lands, etc. The pupils met mans of science, they knowed their preoccupations and science problems from nowadays (figure 2). Fig. 2 - The delivering of conferences The lectured on coastal lands. In other stage, the pupils participated to lectures on coastal lands. They learned: what is a coastal land and how its take form; the species which habits in such places, their adaptations at environment as well these threats and the protection measures that its will taked; the international and national legislation with reference from these and their application; theit statute. The lectures ended with pupils questions showing their interes about nature (figure 3). The maked of trips. With such stock of knowledge concerning coastal lands, the childrens participated to study trips in various protected and other coastal lands from Constantza County (figure 3). The pupils received binoculars, cameras, cases for the measurement of physical and chemical parameters, botanical cases, etc. They achieved observations concerning the phenomenons which happened in these zones. They learned to collect and to determine plants and animals species from respective zones. They learned to make herbariums, insect collections and the others, too. Finally, they understood the species adaptations at such environments (Axini, Bercu, 2006). 154 Fig. 3 – The maked lessons and trips The carrying on by pictures competitions. Its carryed on competitions of pictures, drawings and grapfic arts. The participations were many middle school pupils from Constantza County schools and pre – school childrens from two nursery schools in Constantza Town. The drawing up of instructive teaching aids. In same projects, the pupils received teaching aids concerning the coastal lands: posters, leaflets, booklets, etc. In others projects, the pupils distributed the leaflets with coastal lands informations (figure 4). Fig. 4 - The drawing up of instructive teaching aids The seeing of documentary films. The pupils saw documentary films concerning wild life from coastal places, the dolphins and 2 Mai – Vama Veche Submarine Reservation. The acting of sketchs. The last years, it was written and it staged a little play. The sketch was acted by middle school pupils from „Kemal Atatürk” National High School. The granting of diplomae and prizes of participant pupils in projests. For the implication in conferences, we granted an number of: 5 excellent prizes, 7 prizes I, 6 prizes II, 6 „The Seal of Black Sea” Prizes, 7 „The Dolphin of Sea” Prizes (see table 1). For participation to the competitions of pictures, drawings and grapfic arts, we granted an number of: 4 excellent prizes, 3 prizes I, 5 prizes II, 4 prizes III, 2 mentions and 5 „Lirica M rii” Prizes (see table 2). The great number of diplomae and prizes shows the passion of the pupils and their wish for the knowledge and the protection od nature, of coastal lands in particular. In general, the diplomae maked and financed by G.C.E.E.M. We gives prizes than: popularity science books, atlases, posters, leaflets, instructive teaching aids concerning biology and ecology of coastal lands. Table 1. Diplomae gave the pupils for the active participation to conferences THE PRIZE The Excellent Prize NUMBER OF PRIZES Middle School 2 High School 4 NUMBER OF PUPILS NUMBER OF PAPERS Middle School 2 Middle School 2 155 High School 13 High School 3 The Prize I The Prize II „The Seal of Black Sea ” Prize „The Dolphin of Sea " Prize TOTAL 5 5 - 2 1 6 5 5 - 2 1 15 5 5 - 4 1 6 4 7 4 10 5 2 16 20 16 41 17 16 Table 2. Diplomae gave the pupils for the active participation to pictures, drawings and grapfic arts competitions THE PRIZE NUMBER OF PRIZES NUMBER OF PUPILS NUMBER OF PAPERS The Excellent Prize The Prize I The Prize II The Prize III The „Lirica Marii” Prize Mention TOTAL Middle School 4 Middle School - Middle School 4 High School - Middle School 4 High School 3 5 4 5 - 3 5 4 9 - 3 5 4 5 - 2 23 - 2 27 - 2 23 - - The Foundation of J.T.R. Group In 2007, was born the group of Junior Terrestrial Rangers (J.T.R.), formed by middle school pupils with age between 11 – 15 years. This group is composed by one leader, one spokesman, one environmental reporter and group members. Their mission is the study and the protection of reserves, in general, of nature from Dobrudja by lands studies, conversations with public and the distribution of teaching aids concerning nature informations, etc. Future views Such projects, in special those with practic parts, were a success. All this, its advises us to change them into programs which we are going to develop years by years. The direct beneficiaries will be pupils from others school institutes from Constantza County. In future, we are going to be more pupils in J.T.R. group, to expand their action area and to achieve by experience changes with similar groups both in our country and others. Some of high school pupils will be include in research projects and they even will be to a scientific profession. Collaborations In all this projects, we colaborated with: 1) Faculty of Natural Sciences and Agricultural Sciences – Ph. D., Associate Professor Marius Skolka; 2) Agency of Environment Protection, Constanta – advisers Zoica C l toiu, Mihaela Condur, Marcela Popovici; 3) National Institut For Marine Research And Development „Grigore Antipa”, Constantza, Romania – strategy – cooperation manager, Ph. D. Nicolae Papadopol, biologist Maria Moldoveanu, engineer Ph. D. Laura Alexandrov, engineer Ph. D. Tania Zaharia and others; 4) Museal Complex of Natural Sciences – general manager Decebal F g d u, biologist Ph. D. Elena Şerb nescu, biologist Adela Bologa; 156 5) The national Administration „Romanian Waters” „Dobrogea – Litoral” „Waters Directorate – office leader Josefina Lipan; 6) The Romanian Naval League, Constantza Subsidiary – biologists Ph. D. Ioan and Florica Porumb, contra-admiral George Petre; 7) Consulate General of the Republic of Turkey, Constantza – general consul Haluk Ağca as well with school institutes from Constatza County: 1) „Dimitrie Cantemir” Middle School, Constantza – headmaster, teacher of history Teodora Maria Muşat, teacher of chemistry Marina Marinescu, teacher of geography Neriman Asan, teacher of drawing Bogdan Ionu Ene, teacher of technological education Violeta Cojocaru; 2) „Decebal” Theoretic High School, Constantza – teacher of biology Romica Milea, 3) „George C linescu” Theoretic High School, Constatza – teacher of drawing Bogdan Ionu Ene; 4) „Omnia” High School, Constantza – teacher Ph. D. Carmen Atanasiu; 5) „George Emil Palade” School Group, Constantza; 6) O.N. Nursery School no. 51, Constantza – headmaster Doina Albu; 7) Middle School, Crucea – teacher of Romanian language and literature Carmen Maria Dumitrescu; 8) „Nicolae B lcescu” Theoretic High School, Medgidia – teachers of geography Anca Elena B laşa and Şeila Selim; 9) „Kemal Atatürk” National College, Medgidia - teacher of geography Şeila Selim, teacher of drawing Iuliana Neacşu, schoolmaster Eugenia Ungureanu and 10) „Spiru Haret” Middle School, Medgidia – teacher of biology Felicia Simion, teacher of drawing plastic Iuliana Neacşu; 11) „Laz r Edeleanu” School Group, N vodari – teacher of biology Corina Tudoraş and Middle School no. 3, N vodari. Conclusions The participation of pupils at theoretical and practical activities of these projects show their interest in nature and costal lands, too. They wish to participate at various projects and programes concerning the study, the research and the reconstruction of such zones. References 1. 2. AXINI M., Bercu R, 2006 – Theoretical And Practical Activities Concerning The Development At Pupils Of Conscience Concerning The Coastal Wetlands, JEPE - under press; CORNEANU G. C., Cojocaru L., Corneanu M., 2005 – Quick Testing Methods Of The Environment Mutagen Capacity With The Possibility To Use Them In Schools And In Hospital Units, Journal of Envioronmental Protection and Ecology 6, No 1, 31 – 34; 157 FORMS AND METHODS OF ECOLOGICAL EDUCATION AND UPBRINGING Stefka Georgieva GABROVSKA Yordan Yovkov Primary School, Kavarna, Dobrich District, Republic of Bulgaria __________________________________________________________________________________________ Abstract: The paper deals with aspects of ecological education accomplished through a collaboration among schools and some NGOs from the Dobrich district. This collaboration is materialized through different activities with the pupils: excursions to get acquainted to the biodiversity, participation to cleaning and reforestation campaigns, information campaigns and activities for the dissemination of the information regarding the protection of the environment, biodiversity monitoring activities (especially birds), exhibitions with topics related to biodiversity, etc. Keywords: ecological education, environment, information campaigns, Dobrich district. __________________________________________________________________________________________ Introduction Due to the over-loaded curriculum, the responsibilities of Ecological education and sustainable development are put on the extracurricular activities. They enable reassertion of already acquired knowledge in the field of Ecological studies and create possibilities for the students to participate, in practice, in preservation and restoration of the Environment. Young people should be actively engaged in social activities and should be a part of what is happening in their Municipality and the whole region. This expresses their willingness to live together in clean streets, clean neighborhoods and to have a word on the social changes. Social integration of the young will help them cope with the negative trends of our time, such as self-isolation, anonymity, lack of motivation. Materials and Methods The system of extracurricular work includes components which are divided into two groups: Group 1. Principles, methods, means, stimulus, material, technological and financial provision of the activities within the system. The first three of the stated components are known from Pedagogy but are adapted to the goals of Ecological education and sustainable development. The rest of the components are developed in our school according to the given conditions. Group 2. Forms of work for educating in Ecological and sustainable development concern. The optional course called Ecology and Health works twice a week on an approved curriculum including theoretical and practical activities. The curriculum dwells on the following modules: 1. Black Sea- charm and magic 2. Humid Areas- a laboratory under the open sky 3. Water- the spring of life 4. Love and concern for the Environment 5. Planet Earth- our home The goal of the program is not merely acquiring certain knowledge but also: - to prompt students to value more the Environment in which they live and study; - to understand the importance of every person in finding solutions for ecological problems; - to present positive and healthy ways of living; - to develop a sense of personal responsibility; - to demonstrate the idea of public engagement; - to set up an adequate behavior and interest in research and exploratory activities. 158 The activities planned for the realization of the themes include excursions; meetings with representatives of Biodiversity Foundation , Bulgarian Association for Birds Preservation, lectors from the University of Shumen, Association for Ecology and Sustainable Development-Getia Pontika; forestation and cleaning campaigns; informational, propaganda and preservative work. With this eco district been created, the ideas of the optional course become popular, papers and research themes are written. The young environmentalists take part in eco competitions, quizzes, contests on ecological themes, etc. Ecopulse Club is a constant extracurricular form which tackles environmental issues and sustainable development. It was founded on 4 October 2000. Its members vary from 5th till 8th grade students with special interest in Natural sciences, all enthusiastic environmentalists. By using different methods and forms of education, students have the opportunity to be active in studying the ecological peculiarities, cultural and historic heritage of Black Sea Dobrudja as well as other regions of our country. Symbols of the club are Branta ruficollis and cape Chirakman. The activities of Ecopulse are of both permanent and temporary character but always related to significant dates like: 29 December- International Day of Preserving the Ecological Diversity 22 March- International Day of the Water 22 April- International Day of the Earth 5 June- International Day of Preserving the Environment The club is open for new members and every student who is concerned about the future of our planet is welcomed. The group of members is flexible and its members may depend on the discussed issues, the interests and abilities. The program of the club is realized through interactive education and modern forms and methods of work with a practical orientation- “brain attack”, debate, discussion. The curriculum is based on the knowledge, the skills and the attitude of the students in the different cultural-educational areas. The Environment is considered in its unity and wholeness with emphasis on the three spheres of interaction- natural, social and technological, and on the global challenges of our time. This type of education directs students towards the answers of the questions: “What needs to be done?”, “How does it need to be done?”, “Why does it need to be done?”, “What is my personal role and responsibility?”. The curriculum provide conditions for maximum number of students to be active participants in practical activities concerning preservation and restoration of the Environment In this way, they build up motivation and responsible attitude towards current and possible problems on a regional and national scale. The activities of a temporary character might be eco lecture, excursion, expedition, eco camp, informational and propaganda campaign, preservation activity, working on projects, presentations and conferences. Eco lecture - the themes are logically connected with important dates for the green-minded activists (i.e. 16 September- International Day of Ozone Layer Preservation; 3 October- International Day of Birds; First week of April- The Week of Forests; 15 May- International Day of the Climate; 29 August- the European Night of the Bat, etc.) These dates are good occasion for meetings with specialists and scientists in various fields of knowledge. Guests of Ecopulse Club have been representatives of Bulgarian Association for Birds Preservation, of Group for Studies and Preservation of Bats, ornithologists from Association for Preservation of Humid Areas- Claverock, Scotland. Our students were given the chance to see latest presentations on Birds diversity, on Bulgarian ichthyofauna, on the biological specifics of Branta Leucopsis. Informational and propaganda campaign - it aims raising the ecological consciousness of students, parents, society. With the help of the Board of Trustees of our school, we published flyers of the Youngsters section of Bulgarian Association for Birds Preservation in school, calendars, posters, etc. For the purposes of the Informational and propaganda campaign, we set up a special “eco nook” in the school. Preservation activity - it is oriented towards conservation and reproduction of the Environment Serving these goals, many organized campaigns take place: cleaning the seaside area, around the Turkish bath in Kavarna, which is presently a museum, the pedestrian lane to the seaside; forestation; making and placing rags 159 and bird feed-boxes, etc. Our students take part in such activities with consciously and with a great sense of responsibility. This fact proves that, as a result of the Ecological education, the long way of transition Knowledge of the Environment- Attitude towards the Environment- Behavior is accomplished. Technological and financial provision is a crucial factor for the efficiency of the Ecological education and sustainable development. With this regard, we carry out projects that are often sponsored by the Board of Trustees, the Regional Inspection of Preservation and Control of Public Health- Dobrich, the Association of Ecology and Sustainable Development- Detia Pontika, parents. Eco excursions - they contribute to the connection between the theoretical knowledge acquired from the optional Ecology course and the real natural conditions. Student may have first-hand experience with preserved species when visiting: the lakes in Shabla and Durankulak, cape Kaliakra, the Preserved area of Bolata, Yailata National Archaeological Reserve, Reserve Srebarna, Poda Preserved Natural Center, Atanasovsko Lake close to Burgas, etc. Eco camps - they give students the chance of long-term direct communication with Nature which helps perceiving it fully will all senses. Eco camps are organized after the end of the school year in different bases. The schedule of an Eco camp consists of theoretical studies (lectures, discourses), practical activities with ecological character and time for brakes. Eco camps could be combined with visits to museums, historic monuments, exhibitions, caves and other places of interest in the certain area. Project work - it teaches students to work in a team, to form complex knowledge based on various informational resources, to gather rich practical experience. Students’ active presence in the Monitoring of the regular bird species was materialized in the project International Ecology Forum Srebarna 2006. Their efforts were rewarded with First price for young participants. The last challenge before the students from 4th grade of Yordan Yovkov Primary School is the National students competition named The Project of Our Class for a Life without Cigarette Smoke. We take part in the Smoking Prevention section with the project I Do Not Smoke and I am Independent. On 4 November 2008 we founded a Club of the non-smoker called I Do Not Smoke and I Want the Others to Know It! The activities in the club will be competitions, lectures, presentations, speaking on radio shows, conferences, etc. Our students could compare their progress and awareness of environmental issues with their peers on the following forums: Fifth National Competition in Natural Sciences and Ecology- Dobrich; National Contest “Water- the spring of life”- Burgas: final stage of the National Olympiad of ornithology. Our students were deeply touched and inspired by the example of the Peace Corps volunteers from USA and France whom they met. They also talked to scouts from Varna and Sofia who taught them how to train their endurance, how to put a tent together, how to set fire and to orientate in the wild nature. Results and Discussions It has become a tradition in our school to celebrate 22 April- International Day of the Earth with an exhibition of the biological diversity of Bulgaria. Thus the intertextual connection between Biology, Geography, History, Literature and Art is justified. The purpose of the exhibition is to form a modern notion of the world and to imply the necessity of preserving the ecological balance and the rational use of Nature’s wealth. Its educational idea is to make students aware of at least a part of the valuable resources of Planet Earth, of the diversity of species and, as a result, to recruit new members. On the exhibition in question, abundance of items was presented: 20 paintings; photos; collections of Mollusca; research papers on Galanthus nivalis and Centaurium erythraea as well as on the theme Peoples Actions in Preserving the Endangered Plants; descriptions of favorite sea and river creatures; of favorite flower; essays on the themes Problems In the Environment I Live In, Is Life Possible on Earth without Photosynthesis? After studying about Magnoliopsida and Liliopsida in the regular Biology classes for 7th grade, the optional course continues the theme by gathering and organizing herbarium. Now our collection consists of: Rosaceae- Rubus idaeus, Rosa canina, Agrimonia eupatoria, Cydonia oblonga; Asteraceae- Bellis perennis, Achillea millefolium, Matricaria chamomilla, Cirsium arvense, Ranunculaceae- Consolida regalis, Clematis 160 vitalba; Ranunculus repens, Ficaria verna, Aquilegia vulgaris; Liliaceae- Convallaria majalis, Asparagus officinalis; Poaceae- Poa pratensis, Cynodon dactylon, Setaria glauca. Consistent observations lead to the students’ ability of unmistakably identifying the following bird species: Phalacrocoeax carbo, Fulica atra, Larus cachinnans, Motacilla cinerea, Alcedo atthis, Corvus monedula, Dendrocopos syriacus, Oriolus orilus, Carduelis chloris, Merops apiaster, Melanocorypha calandra, Carduelis carduelis, Hirundo rustica. Conclusions Working with children is a responsibility as well as a motivation. Not once have they provoked me with their own ideas resulting from their touch with books, with popular science films, with Internet. It is of great importance to have these ideas in mind and to impress on young people that the future of our planet depends on our current behavior. References 1. 2. 3. PETROV, S., PALAMAREV, E., 1989, Atlas on Botanic, Narodna Prosveta Publishing House, pgs. 120, 255, 278, 301 STANEVA, D., PANOVA, D., 1986, The Herbs in Every House, Medicine and Physical Culture, pg. 28 *** Center for Education, Culture and Ecology “21”, Interactive Education in Ecology and Sustainable Development, 2003, Volume І, Varna, pg. 53-55 161