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Botanica Marina 2023; 66(4): 239–269 Review Ka-Lai Pang*, E. B. Gareth Jones*, Mohamed A. Abdel-Wahab, Sarah J. Adams, Artur Alves, Egídia Azevedo, Ali H. Bahkali, Margarida Barata, Gaëtan Burgaud, Maria Filomena Caeiro, Mark S. Calabon, Bandarupalli Devadatha, Joëlle Dupont, Sally C. Fryar, Maria C. González, Jing Jin, Mohamed Mehiri, Laurence Meslet-Cladière, Soizic Prado, Teppo Rämä, Marlis Reich, Catherine Roullier, Vemuri Venkateswara Sarma, Leif Tibell, Sanja Tibell, Patricia Velez and Allison K. Walker Recent progress in marine mycological research in different countries, and prospects for future developments worldwide https://doi.org/10.1515/bot-2023-0015 Received March 12, 2023; accepted June 2, 2023; published online June 27, 2023 Abstract: Early research on marine fungi was mostly descriptive, with an emphasis on their diversity and taxonomy, especially of those collected at rocky shores on All authors contributed equally to this paper. *Corresponding authors: Ka-Lai Pang, Institute of Marine Biology and Centre of Excellence for the Oceans, National Taiwan Ocean University, 2 Pei-Ning Road, Keelung 202301, Taiwan, ROC, E-mail: klpang@ntou.edu.tw ; and E. B. Gareth Jones, Department of Botany and Microbiology, College of Science, King Saud University, P.O Box 2455, Riyadh 11451, Kingdom of Saudi Arabia, E-mail: torperadgj@gmail.com. https://orcid.org/0000-00027286-5471 (E.B.G. Jones) Mohamed A. Abdel-Wahab, Department of Botany and Microbiology, Faculty of Science, Sohag University, Sohag 82524, Egypt. https://orcid.org/ 0000-0002-3176-8675 Sarah J. Adams and Allison K. Walker, Department of Biology, Acadia University, Wolfville, NS, Canada. https://orcid.org/0000-0002-5061-361X (A.K. Walker) Artur Alves, Centro de Estudos do Ambiente e do Mar (CESAM), Departamento de Biologia, Universidade de Aveiro, 3810-193 Aveiro, Portugal Egídia Azevedo, Centro de Ecologia, Evolução e Alterações Climáticas (CE3C), and Centro de Estudos do Ambiente e do Mar (CESAM), Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal Ali H. Bahkali, Department of Botany and Microbiology, College of Science, King Saud University, P.O Box 2455, Riyadh 11451, Kingdom of Saudi Arabia Margarida Barata, Centro de Ecologia, Evolução e Alterações Climáticas (CE3C), Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal Gaëtan Burgaud and Laurence Meslet-Cladière, Univ Brest, INRAE, Laboratoire Universitaire de Biodiversité et Écologie Microbienne, F-29280 Plouzané, France Maria Filomena Caeiro, Centro de Estudos do Ambiente e do Mar (CESAM), Departamento de Biologia Vegetal, Faculdade de Ciências, Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal. https:// orcid.org/0000-0003-0559-6344 Open Access. © 2023 the author(s), published by De Gruyter. seaweeds and driftwood. Subsequently, further substrata (e.g. salt marsh grasses, marine animals, seagrasses, sea foam, seawater, sediment) and habitats (coral reefs, deepsea, hydrothermal vents, mangroves, sandy beaches, salt marshes) were explored for marine fungi. In parallel, research areas have broadened from micro-morphology to ultrastructure, ecophysiology, molecular phylogenetics, Mark S. Calabon, Division of Biological Sciences, College of Arts and Sciences, University of the Philippines Visayas, Miagao, Iloilo 5023, Philippines. https://orcid.org/0000-0002-6603-1876 Bandarupalli Devadatha and Vemuri Venkateswara Sarma, Department of Biotechnology, School of Life Sciences, Pondicherry University, Pondicherry, India. https://orcid.org/0000-0001-6400-5407 (B. Devadatha) Joëlle Dupont, Muséum National d’Histoire Naturelle, Institut de Systématique, Evolution et Biodiversité, ISYEB – UMR 7205 – CNRS, MNHN, UPMC, EPHE, Muséum National d’Histoire Naturelle, Sorbonne Universités, CP39, 75231 Paris Cedex 5, France Sally C. Fryar, College of Science and Engineering, Flinders University, GPO Box 2100, Adelaide, SA 5001, Australia. https://orcid.org/0000-0002-95127666 Maria C. González and Patricia Velez, Departamento de Botánica, Instituto de Biología, Universidad Nacional Autónoma de México, Mexico City, Mexico Jing Jin, College of Plant Health and Medicine, Qingdao Agricultural University, Qingdao, Shandong, 266109, China Mohamed Mehiri, Marine Natural Products Team, Institut de Chimie de Nice, Université Côte d’Azur, CNRS UMR 7272, 06108 Nice, France Soizic Prado, Muséum National d’Histoire Naturelle, Unité Molécules de Communication et Adaptation des Micro-organismes, UMR 7245, CP 54, 57 rue Cuvier, 75005 Paris, France Teppo Rämä, Marbio, UiT, The Arctic University of Norway, Tomsø, Norway Marlis Reich, Molecular Ecology, FB2, University of Bremen, Bremen, Germany Catherine Roullier, Nantes Université, Institut des Substances et Organismes de la Mer, ISOMER, UR 2160, F-44000 Nantes, France Leif Tibell and Sanja Tibell, Systematic Biology, Dep. of Organismal Biology, Evolutionary Biology Centre, Uppsala University, Norbyvägen 36, 75236 Uppsala, Sweden. https://orcid.org/0000-0003-4143-9856 (S. Tibell) This work is licensed under the Creative Commons Attribution 4.0 International License. 240 K.-L. Pang et al.: Country reports of marine mycological research biogeography, biodeterioration, biodegradation, bioprospecting, genomics, proteomics, transcriptomics and metabolomics. Although marine fungi only constitute a small fraction of the global mycota, new species of marine fungi continue to be described from new hosts/substrata of unexplored locations/habitats, and novel bioactive metabolites have been discovered in the last two decades, warranting a greater collaborative research effort. Marine fungi of Africa, the Americas and Australasia are underexplored, while marine Chytridiomycota and allied taxa, fungi associated with marine animals, the functional roles of fungi in the sea, and the impacts of climate change on marine fungi are some of the topics needing more attention. In this article, currently active marine mycologists from different countries have written on the history and current state of marine fungal research in individual countries highlighting their strength in the subject, and this represents a first step towards a collaborative inter- and transdisciplinary research strategy. Keywords: Ascomycota; Basidiomycota; ecology; ecosystem; fungal community 1 Introduction Since our last update on the number of marine fungi (Jones et al. 2019), 641 species in 231 genera have been added, bringing the current total to 1898 species (Calabon et al. this issue). Although this number constitutes only a little over 1 % of the global diversity of fungi (Phukhamsakda et al. 2022), it represents the hard work of a consortium of mycologists over the last 150 years to look for this fascinating group of fungi with unique morphology in different marine habitats/niches and substrata all around the world (Jones et al. 2015). Barghoorn and Linder (1944) studied marine fungi of Massachusetts, and this study triggered a significant interest in the fungal group, especially in America and Europe (Denmark, UK). Marine mangrove fungi have attracted much interest since the study by Cribb and Cribb (1955). Subsequently, a wealth of new species has been described from mangrove habitats in tropical and subtropical countries, such as Hong Kong (Pang et al. 2016), Thailand (Jones et al. 2006), Taiwan (Pang et al. 2011b), and Malaysia (Alias and Jones 2010; Lee et al. 2012). In recent years, new researchers have documented the marine fungi of Portugal (Azevedo et al. 2010; Barata 2002), Norway (Pang et al. 2011a; Rämä et al. 2014a,b) and Italy (Panno et al. 2013). Early research on marine fungi was mostly descriptive, with an emphasis on their diversity and taxonomy (e.g. Barghoorn and Linder 1944; Jones 1962, 1968; Kohlmeyer and Kohlmeyer 1964, 1971). Ultrastructure (both scanning and transmission electron microscopy) of ascospores and ascospore appendages was used extensively to delineate species of marine fungi, especially those in the Halosphaeriaceae with diverse ascospore appendage morphology (summarized in Jones 1995). Spatafora and Blackwell (1994) were the first to use a sequence of a marine fungus in the Halophaeriaceae (Halosphaeriopsis mediosetigera) in a phylogenetic study and found it grouped with the Microascales. Sequence data, either from the ribosomal RNA gene cluster or protein genes, have significantly improved the classification of marine fungi (Jones et al. 2009, 2015, 2019). With the advancement of high throughput sequencing, environmental DNA from various substrata in the ocean has revealed a high diversity of marine fungi, in particular, the vast diversity of marine Chytridiomycota and allied taxa (Abdel-Wahab et al. 2021a; Comeau et al. 2016). This article is a community effort to report the history and current state of research in marine mycology by experts of their respective countries. Active marine mycologists are studying different topics of mycology in Africa (Egypt), Asia (China, Hong Kong, India, Malaysia, Philippines, Saudi Arabia, Taiwan, Thailand), the Americas (Canada, Mexico, United States), Europe (France, Germany, Italy, Norway, Portugal, Sweden, United Kingdom) and Australasia (Australia), from ecology, systematics and biotechnology of marine fungi in habitats from the coasts to the deep-sea. Many of the countries listed in this section also hosted the 15 meetings of the International Marine Mycology Symposium (IMMS: see www.marinefungi.com). Similarly, other organisations have included marine fungi in their research programmes and meetings, for example, the Organisation for Economic Co-operation and Development (OECD) working groups on the biodeterioration of materials in marine environment (Furtado and Jones 1980; Jones 1971; Jones et al. 1972). This article is a first step to encourage discussion on topics related to marine mycology and to promote international collaborations, knowing the research strength/ interest of each laboratory. Collaborative grants such as Biodiversa+ (https://www.biodiversa.eu/) are available every year for international marine mycologists to apply. This review gives an account of past and current research in marine mycology, highlighting key mycologists and major research findings, provides a comprehensive reference list of published papers, and offers ideas on future research topics in marine mycology. K.-L. Pang et al.: Country reports of marine mycological research 2 Africa 2.1 Egypt (M.A. Abdel-Wahab) The pioneer Egyptian marine mycologist Anwar Abdel Aleem (University of Alexandria, Egypt) studied marine fungi from various parts of the world: UK (Aleem 1950a), France (Aleem 1950b,c, 1952a,b), Sweden (Aleem 1952c, 1953), Russia (Aleem 1962), Romania (Aleem 1974, 1975), Saudi Arabia (1978) and Sierra Leone (Aleem 1980a; Aleem and Malibari 1981). Aleem (1980b) reported the first marine stramenopile, Pythium marinum, infesting Porphyra leucosticta in the Mediterranean Sea, Egypt. Subsequently, Scott Schatz (Institute of Marine Sciences, University of North Carolina) described Adomia avicenniae from pneumatophores of Avicennia marina from both Australia and Egypt (Schatz 1985). Mohamed A. Abdel-Wahab started his MSc in 1993 studying marine fungi colonizing different substrata at three mangrove sites along the Red Sea coast in Egypt. He recorded 50 marine fungi (47 sexual and asexual ascomycetes, one basidiomycete and two straminopiles) from decaying driftwood, intertidal wood of Avicennia marina, decaying seaweeds and sediment samples. All recorded fungi are new for Egypt and the research work resulted in the following publications: Abdel-Wahab (2005) and El-Sharouny et al. (1998, 1999). Abdel-Wahab (2000), during his PhD study, recorded 26 species from 432 samples collected from three mangrove sites: Abu-Mingar, Safaga and Sharm El-Sheikh. He exposed test blocks of Bruguiera parviflora, Kandelia candel and Sonneratia alba at Safaga mangroves at three tidal levels and this yielded 11 species. During his PhD study, three new species were described (Abdel-Wahab et al. 2001a,b). Abdel-Aziz (2004) studied diversity of aquatic fungi from seven water bodies in Egypt, that ranged between freshwater (River Nile) and the salinity of the open ocean (Qaroun Lake). She recorded 184 species from the seven study sites, of which 150 were new records for Egypt. Abdel-Wahab (2005) examined diversity of marine fungi on intertidal decayed wood of Avicennia marina and on decayed prop roots of Rhizophora mucronata at six mangrove stands along the Red Sea coast in Egypt; 39 species were recorded in his study, of which 19 were new records. Abdel-Wahab et al. (2009) described two new Corollospora species, C. anglusa and C. portsaidica, which were isolated from the coast of the Mediterranean Sea, Egypt. Abdel-Aziz (2010) identified 31 species (19 ascomycetes and 12 asexual fungi) with 21 new records from 100 driftwood samples collected from two sandy beaches at the Mediterranean Sea. Corollospora maritima was the most common fungus found during her 241 study. Abdel-Wahab et al. (2010) described three new asexual genera and species: Halazoon (H. melhae), Moleospora (M. maritima) and Moheitospora (M. fruticosae, later transferred to Juncigena as J. fruticosae; Réblová et al. 2016) from the Mediterranean Sea coast of Egypt. Abdel-Aziz (2008) studied the diversity of aquatic fungi in Lake Manzala (brackish lake). Sixty taxa with 19 new records for Egypt, including 26 ascomycetes and 34 asexual ascomycetes, were recorded from 300 samples collected from three sites of Manzala Lake. El-Sharouny et al. (2009) studied the fungal diversity of brackish and saline lakes in Egypt; 97 species (40 ascomycetes, 55 asexual fungi and 2 basidiomycetes) with 70 new records for Egypt were identified from 764 fungal collections recorded in 545 samples from Lakes Edku, Marriott, Burullus and Qaroun. Nour El-Din (2022) recorded 70 marine fungi (35 ascomycetes, 33 asexual fungi and two basidiomycetes) from 2400 decaying submerged herbaceous and wood samples that were collected from Qaroun Lake. Seven recorded fungi were novel to science, of which Qarounispora grandiappendiculata was formally described (Nour El-Din et al. 2022). Recently, Bakhit and Abdel-Wahab (2022) described the new genus and species, Safagamyces marinus from decaying stems of Phragmites australis collected at Safag mangrove, Egypt. 3 Americas 3.1 Canada (S.J. Adams and A.K. Walker) Marine mycology in Canada began in the late 1960s with studies of intertidal lignicolous fungi from Newfoundland (1968) and British Columbia (1969) by Gilbert C. Hughes of the University of British Columbia, who further studied the geographical distribution of marine fungi (Hughes 1974, 1975). In the following decades, most marine mycology in Canada was conducted on the Atlantic coast by both Canadian and American mycologists. The students of Darryl W. Grund (Acadia University, in Nova Scotia) studied lignicolous marine fungi from marine inundated wood along the coastline (Neish 1970) and in the saltmarshes of the Minas Basin (Boland and Grund 1979). J. David Miller and Norman J. Whitney (University of New Brunswick) then completed a series of papers investigating marine fungal diversity in seawater, macroalgae, marine sediments and salt marsh grasses throughout the Bay of Fundy and the coast of Prince Edward Island. Growth characteristics and metabolites of several marine fungi were described, the new species Didymosphaeria lignomaris was characterized (Miller and 242 K.-L. Pang et al.: Country reports of marine mycological research Savard 1989; Miller and Whitney 1981a,b,c, 1983; Miller et al. 1984; Strongman et al. 1985) and thraustochytrids were documented from seawater (Miller and Whitney 1981d). Felix Bärlocher (Mount Allison University, New Brunswick) further investigated the fungal diversity of Spartina alterniflora and the impacts of these fungi and the snail Littoria saxatalis on smooth cordgrass growth and decomposition (Bärlocher and Moulton 1999; Bärlocher et al. 1989; Mansfield and Bärlocher 1993; Samiaji and Bärlocher 1996). Trussell and Jones (1970) investigated the role of marine fungi in the decomposition of wood in the sea. Since the early 2010s, growing interest in the chemical compounds produced by fungi adapted to the North Atlantic and Arctic Oceans led to increased research on natural product discovery. David Overy and Russell Kerr (University of Prince Edward Island), Alyssa Grunwald (Atlantic Veterinary College), and Andrew Flewelling, Christopher Gray and John Johnson (University of New Brunswick) led the isolation of marine fungi from seafoam, marine sediments and macroalgae, and description of antimicrobial and other chemical compounds (Flewelling et al. 2013; Grunwald et al. 2016, 2017; Morehouse et al. 2020; Overy et al. 2014, 2019). Recent advances in sequencing and bioinformatic techniques allowed detection of novel chytrid lineages from marine environments led by Andre Comeau, Dalhousie University (Comeau et al. 2016). The new marine fungus Lulworthia fundyense was recently described from marine inundated wood (Taylor et al. 2022). Allison Walker and her students at Acadia University also characterized Spartina rhizosphere fungi, including arbuscular mycorrhizae in Nova Scotia salt marshes (d’Entremont et al. 2021), fungi and microarthropods in Spartina decomposition (Malloch et al. 2022), littoral zone lichens (Vail and Walker 2021) and algicolous fungi (Cooper and Walker 2022) from the Bay of Fundy. Currently, over 300 species of marine fungi are known from Atlantic Canada. fungi from coastal habitats, mainly mangroves and sandy beaches. Interestingly, during these explorations the Kohlmeyers noted that the marine coasts of Mexico harbor a high and unregistered diversity of fungi. A decade later, Kevin Hyde described a new manglicolous genus (Falciformispora), and two new species: F. lignatilis and Trematosphaeria lineolatispora in the State of Colima on the Pacific Ocean coast (Hyde 1992a). In the early 1990s, Maria C. Gonzalez was enrolled in the Graduate Biology Sciences Program under the tuition of Teofilo Herrera and Jan Kohlmeyer to study the biodiversity of arenicolus marine fungi on sandy beaches of Mexico. Her research deals mainly with the exploration and taxonomy of culturable marine fungi from sandy beaches, mangroves, and associated fungi on coral reefs. A few graduate students successfully completed their studies under her tuition, including: Patricia Velez (sandy beach marine fungi, and population genetics of Corollospora), María Cristina Medina Ortiz (diversity of coral reef associated fungi) and Carlos Alpuche González (diversity of mangrove marine fungi). Velez continued her studies with the exploration of diversity (sandy beaches, deep-sea, oxygen minimum zones, and hydrothermal vents), molecular ecology, bioremediation, and genetics of Corollospora. At present, marine mycology at the Institute of Biology continues as the first successfully developed research program in Mexico. González et al. (2001) listed a total of 62 species (in 41 genera) of marine fungi in Mexico, including 47 ascomycetes (in 29 genera), one basidiomycete and 14 asexual fungi (in 11 genera). Velez et al. (2013, 2015) added two new records of marine fungi, Arenariomyces majusculus and Ceriosporopsis capillacea. Recently, an updated checklist of the marine fungi of Mexico was published (Portillo-Lopez and GonzalezMartinez 2021). 3.2 Mexico (M.C. González) ‘Marine fungi: their taxonomy and biology’ (Barghoorn and Linder 1944) was a seminal work on marine mycology in the United States. T.W. Johnson completed work during the 1950s–60s on marine lignicolous fungi, ascomycetes and hyphomycetes found on wood and Spartina (e.g. Johnson 1958). In 1961, he co-authored the comprehensive book ‘Fungi in oceans and estuaries’ with F.K. Sparrow who had discovered thraustochytrids in 1934. S.P. Meyers and E.S. Reynolds were responsible for additional effort on marine lignicolous fungi (Meyers and Reynolds 1957, 1959). Meyers (1974) then characterized species associated with seagrasses and saltmarsh grasses. D. Ahearn, F.J. Roth and J.W. Fell Despite nearly 60 years of study, much of the diversity of marine fungi in Mexico still remains to be discovered. The first exploration was by Jan Kohlmeyer (1966), when he collected several species of marine fungi from mangroves located in the State of Veracruz on the Gulf of Mexico coast. The publication of that expedition in 1966 established the beginning of marine mycology in Mexico. In collaboration with Erika Kohlmeyer and Brigitte Volkmann-Kohlmeyer, Jan Kohlmeyer undertook several expeditions in the period 1971–1993, registering several species of Mexican marine 3.3 United States of America (S.J. Adams and A.K. Walker) K.-L. Pang et al.: Country reports of marine mycological research completed pioneering work on marine yeasts isolated from marine sediments, water, seagrass and invertebrates (Fell et al. 1960; Roth Jr. et al. 1962). R.V. Gessner completed extensive taxonomic characterization of fungi associated with cordgrass (Spartina) from salt marshes along the Atlantic coast of the US and Canada (Gessner 1976, 1977; Gessner and Goos 1973; Gessner and Kohlmeyer 1976). Carol Shearer, a leading authority on aquatic ascomycetes, began her career researching the distribution and taxonomy of lignicolous ascomycetes of the Chesapeake Bay (Shearer and Crane 1971), and proceeded to document a wide range of marine fungi. Steve Newell later completed long-term studies on the role of marine fungi in the decomposition of saltmarsh grass, using ergosterol as a proxy for fungal biomass (Newell 1993; Newell et al. 1987). Joey Spatafora’s phylogenetic studies refined our understanding of marine fungal evolution, resulting in the removal of the genera Lindra and Lulworthia from the Halosphaeriaceae (Kohlmeyer et al. 2000; Spatafora et al. 1998). Jinx Campbell worked on phylogenetic studies on multiple orders of marine fungi (Campbell 2005; Campbell et al. 2003, 2005, 2009; Walker and Campbell 2010). Jan Kohlmeyer, with a research career spanning more than 70 years, was a giant of North American marine mycology. The Kohlmeyers (including Erika Kohlmeyer and Brigitte Volkmann-Kohlmeyer) described 149 species, 50 genera, four families and four new orders of marine fungi, in 158 papers and four books. Their collections are preserved at the New York Botanical Garden. ‘Marine mycology: the higher fungi’ (Kohlmeyer and Kohlmeyer 1979) was one of the first comprehensive publications to combine literature, monograph genera and species and remains an indispensable reference. An international marine fungi workshop held at the Marine Biological Laboratory (Woods Hole, MA) led to the publication of ‘Fungi in the marine environment: open questions and unsolved problems’, providing a new focus for global marine mycological research (Amend et al. 2019). Identification of genes responsible for biomass degradation and fungal assimilation of nitrogen was undertaken to better understand the role of fungi and the oceanic ‘mycoloop’, re-assessing fungal biogeographical processes, revision of their taxonomy and improving protocols for isolating marine fungi as well as highlighting further research topics. Current American marine mycological research features global collaborations led by Anthony Amend (Hawaii) on patterns of biogeography, community phylogenetics and fungal biodiversity (Gladfelter et al. 2019; Tisthammer et al. 2016; Wainwright et al. 2017); Brandon Hassett on Arctic marine fungal communities; their spatial distribution, ecological roles and functional genetics (Hassett et al. 2017, 2019; Rämä et al. 2017), 243 Cassie Ettinger (California) on Zostera marina – associated fungi (Ettinger and Eisen 2020; Ettinger et al. 2021) and Amy Gladfelter (UNC) on marine fungal cell division using timelapse imagery (Gladfelter et al. 2019; Mitchison-Field and Gladfelter 2021; Mitchison-Field et al. 2019). 4 Asia 4.1 China (J. Jin and E.B.G. Jones) Although China has a long coastline and many renowned mycologists, few have ventured to examine its marine fungal diversity. The first reports are those of Lilian Vrijmoed who collected marine fungi on Hainan Island (Vrijmoed et al. 1996). Liu et al. (2010) documented the phylogenetic diversity of culturable fungi associated with two marine sponges: Haliclona simulans and Gelliodes carnosa, also collected at Hainan Island. Jin et al. (2004a,b) presented preliminary data on marine fungi from wood substrata collected at various locations along the coast of the Yellow Sea and extended knowledge of their occurrence in China. Jin et al. (2005) reported on the collection of Dryosphaera navigans and Torpedospora radiata from the Yellow Sea, both new records for China. There then followed a series of papers documenting marine fungi of China (Diao et al. 2009; Du and Jin 2010; Qiao and Jin 2011; Sun et al. 2008a,b; Yang et al. 2009a,b). Jin and Huang (2009) reported on the collection of Monosporascus cannonballus in the marine environment for the first time. In total some 142 species in 74 genera were reported on driftwood and intertidal wood collected from the Bohai Sea and the Yellow Sea, China, of which 8 genera and 36 species were regarded as new records for China. Moving on a decade, studies involved molecular techniques in documenting marine fungi in the deep sea and resulted in a number of publications from the Institute of Oceanography, Xiamen, and collaborating institutions. Xu et al. (2014, 2016) reported on the fungal diversity of deep-sea sediments of the Pacific Ocean as assessed by comparison of ITS, 18S and 28S ribosomal DNA regions. Further studies documented deep-sea fungi associated with chimney and sulfide samples from a South Mid-Atlantic Ridge hydrothermal site (Xu et al. 2017); those on deep-sea sediments of a hydrothermal vent system in the Southwest Indian Ridge (Xu et al. 2018) and fungi in the deep-sea hadal sediments of the Yap Trench (Xu et al. 2019). In the early 2000s, a collaborative research programme was established between Prof. Yong-Cheng Lin and his colleagues at Sun Yat Sen (Zhongshan) University, Guangzhou with Prof. Lilian Vrijmoed at the City University of Hong 244 K.-L. Pang et al.: Country reports of marine mycological research Kong. This resulted in the discovery of many novel compounds such as: N-cinnamoylcyclopeptide (Lin et al. 2001a), xyloketals (Lin et al. 2001b), gamma-lactone, eutypoid-A (Lin et al. 2002a), 1-(2,6-dihydroxyphenyl), isocoumarins from the mangrove endophytic fungus #2533 (Lin et al. 2001c), eniatin G from the mangrove fungus Halosarpheia sp. (#732) from the South China Sea (Lin et al. 2002b) and butanone (Huang et al. 2005), along with many others. Many other centers are investigating marine fungi in China including: College of Marine Life Sciences, Ocean University of China, Qingdao; College of Food Science and Technology, Guangdong Ocean University; the State Key Laboratory of Mycology, Institute of Microbiology, Beijing; Department of Biology, Shaoxing University, Shaoxing; Shenzhen Key Laboratory of Microbial Genetic Engineering, Shenzhen University (Han et al. 2022; Wang et al. 2016, 2017; Wu et al. 2023; Zhang et al. 2021; Zhou et al. 2016). Zhang and colleagues (Shi et al. 2021) have sequenced whole genomes of seven fungi (Westerdykella dispersa, Trichoderma lixii, Aspergillus tubingensis, Penicillium brefeldianum, Neoroussoella solani, Talaromyces fuscoviridis, Arthrinium marii) isolated from rhizospheres of two mangrove plants (Acanthus ilicifolius and Kandelia obovata) from East Harbour National Nature Reserve (Hainan, China). They were able to identify gene clusters for carbohydrate active enzymes and secondary metabolite biosynthesis. (molecular phylogeny of the Halosphaeriaceae). Steve Pointing joined the group as a research fellow and Mohamed Abdel-Wahab undertook much of his field work in Hong Kong for his PhD. After the retirement of Lilian Vrijmoed, research on marine fungi has been discontinued. In November 1992, Kevin Hyde was appointed to a tenured Associate Professorship at the Department of Ecology and Biodiversity, University of Hong Kong, and continued with his contributions to marine mycology. Studies included the taxonomy of mangrove fungi, with a number of graduate students/post-doctoral researchers: Sally Fryar (brackish water in Brunei and Philippines), Vivienne Bucher (wood decay of marine fungi), V.V. Sarma (marine fungi in Spartina and mangroves), A.D. Poonyth (taxonomy of marine fungi in Mauritian mangroves), M.V. Ranghoo (phylogeny of aquatic fungi), M.O.K. Poon (intertidal mangrove fungi) and studies by T.K. Goh (taxonomy of mangrove asexual fungi). Steve Pointing also joined University of Hong Kong to carry on his studies on the lignocellulose-degrading marine fungi. With Kevin’s move to Thailand in 2007, studies on marine fungi at the University of Hong Kong ceased. Pang et al. (2016) listed a total of 141 species (in 96 genera) of marine fungi in Hong Kong, including 125 ascomycetes (in 83 genera), 3 basidiomycetes (in 3 genera) and 13 asexual fungi (in 10 genera). 4.2 Hong Kong (K.L. Pang and E.B.G. Jones) 4.3 India (B. Devadatha and V.V. Sarma) Marine mycology in Hong Kong was initiated by Prof. Peter Thrower and Lilian Vrijmoed studying for the PhD degree which was awarded in 1983 (Vrijmoed 1983). This led to British Council exchanges and the first joint publications on marine fungi (Vrijmoed and Jones 1993). In 1996, Gareth Jones joined the City University of Hong Kong as the Royal Society Kan Tong Po Visiting Professorship and thus the establishment of a strong research group. During this period, City University of Hong Kong hosted the 7th International Marine Mycology Symposium in 1999. It was one of the largest meetings of this group (see www.marinefungi.com). Studies included potential development of thraustochytrids as a source of polyunsaturated fatty acids (PUFAs), mangrove fungal ecological studies and taxonomic studies, wood decay by marine fungi and early studies of fungi on bamboo. A few graduate students successfully completed their studies: Eduardo Leaño (ecology of Halophytophthora species in mangrove), Rex Sadaba (mangrove fungal ecology), Keith Fan (thraustochytrids in Hong Kong mangroves and their potential use for PUFAs production), Wen Luo (wood-degrading enzymes of marine fungi), Ka-Lai Pang In India, marine fungal studies were carried out on various substrata such as algae, animals, driftwood, intertidal wood, sea grasses, sea foam, mangrove wood, sediments and water. Early research was descriptive: Antennospora quadricornuta on small fishing boats at the coasts of Kerala and Chennai (Becker and Kohlmeyer 1958), Paraliomyces lentiferus (new genus and species) on wooden fishing boats from Chennai (Kohlmeyer 1959), and Corollospora pulchella from the Kerala coast (Kohlmeyer et al. 1967), while Jones (1968) recorded five marine fungi from test blocks of wood immersed near the shores of Mumbai and Kochi coasts. Nair (1970) was the first Indian scientist to investigate marine fungi on intertidal wood from the Kerala coast. Raghukumar (1973) was the first Indian researcher to examine marine fungi on intertidal decomposing mangrove wood from the Tamil Nadu coast and reported 18 species of Ascomycota. Seshagiri Raghukumar completed his PhD on marine fungi from Tamil Nadu coast in 1973 at Madras University under the supervision of C.V. Subramanian. He later studied the ecology and taxonomy of thraustochytrids with Alwin Gaertner. Later at the CSIR National Institute of K.-L. Pang et al.: Country reports of marine mycological research Oceanography, Goa, India, he began with detailed studies on the role of fungi in the marine detrital food web (Raghukumar 2005) and the seasonal dynamics of thraustochytids of the Arabian Sea. Raghukumar made significant contributions to the ecology of these stramenopilan fungi (Raghukumar 2002; Raghukumar and Damare 2011) and, in particular, he developed a novel epifluorescence technique to detect and quantify thraustochytrids in seawater and marine samples (Raghukumar and Schaumann 1973). His students who graduated in marine fungal studies include Varada Damare (ecology and molecular characterization of thraustochytrids and aplanochytrids from oceanic water column; Damare and Raghukumar 2006), Veena Sathe (ecological investigations on fungi associated with detritus from marine macrophytes) and Ruchi Jain (polyunsaturated fatty acids and extracellular polymeric substances from thraustochytrid protists). Chandralata Raghukumar graduated with a PhD in Plant Pathology from Madras University in 1975 and subsequently worked at the Institute for Marine Research, Bremerhaven, Germany for five years, where she began to work on fungal diseases of algae with Alwin Gaertner. Later at the CSIR-National Institute of Oceanography, Goa, India, she undertook studies on fungal diseases of marine algae along the coast of Goa, describing numerous algal diseases not reported till then (Raghukumar 1986). Raghukumar et al. (1992) isolated several higher marine fungi and thraustochytrids from surface-sterilized macroalgae. She was a pioneer in studying fungi in deep-sea marine sediments. Together with her students, she carried out various research studies on diversity and biology of deep-sea fungi from the Central Indian Ocean Basin (CIOB) at a depth of 5000 m; Damare et al. (2006) and Singh et al. (2012) isolated a number of fungi, the majority of which belonged to the genera Aspergillus, Penicillium, and Cladosporium. Another important area of her research was on the role of fungi in the oxygen minimum zone of the Arabian Sea, where Manohar and Raghukumar (2013) reported marine fungal diversity and anaerobic denitrification of fungi from coastal marine sediments of Goa. She also pioneered the study of fungi in hard corals of the Lakshadweep islands, along with J. Ravindran (Raghukumar and Ravindran 2012). B.D. Borse and colleagues studied marine fungi of mangroves extensively and described many new species: Didymella avicenniae and Halosarpheia ratnagiriensis (now Saagaromyces ratnagiriensis) (Patil and Borse 1983), Aigialus mangrovis, A. rhizophorae and Pleospora avicenniae (now Halojulella avicenniae) (Borse 1984, 1985, 1987), Acrocordiopsis patilii (new genus) (Borse and Hyde 1989), Biatriospora marina (new genus) and Massarina velataspora (now Morosphaeria velataspora) (Hyde and Borse 1986a, 245 1986b). Borse et al. (2013) listed 207 marine fungi recorded along the coastal states and islands of India. B.P.R. Vittal from University of Madras, Chennai and his students M. Ravikumar and V.V. Sarma also investigated marine mangrove fungi of India focusing on frequency of occurrence, host specificity, substrate recurrence, vertical distribution and seasonality (Sarma and Vittal 1998–1999, 2000, 2001, 2002; Sarma et al. 2001; Vittal and Sarma 2006), and introduced the new species Lophiostoma mangrovei (now Rimora mangrovei) (Kohlmeyer and Vittal 1986) and Bathyascus mangrovei (Ravikumar and Vittal 1991). Sarma and Vittal (2004) proposed a dichotomous key to 88 marine fungi recorded from mangroves of Godavari and Krishna deltas, east coast of India and developed an interactive CD-ROM for mangrove fungi, which included 85 mangrove fungi from Indian and Hong Kong mangroves (Sarma et al. 2000). In 2009, V.V. Sarma acquired a faculty position at Pondicherry University, India where he is now conducting research in the field of fungal biotechnology. His student B. Devadatha studied the biodiversity, morpho-molecular characterization of marine fungi in India and their antiquorum sensing potential. This resulted in five novel genera, namely Halocryptosphaeria, Pseudoastrosphaeirellopsis, Raghukumaria, Thyridariella and Vittaliana, and 25 new marine fungal species (Devadatha et al. 2017, 2018, 2019, 2021a; Dayarathne et al. 2020a). K.R. Sridhar completed his doctorate in Biosciences from Mangalore University. He made significant contributions to the fields of freshwater, mangrove, and marine mycology in India (Sridhar and Kaveriappa 1988, 1991). Ananda and Sridhar (2002) documented 10 ascomycetes and one basidiomycete on intertidal mangrove wood, and studied endophytic fungi in roots of mangrove plants from Udyavara mangroves (Ananda and Sridhar 2002). Prasannarai et al. (2000) described a new species Corollospora indica on intertidal wood, and Maria and Sridhar (2002) introduced Passeriniella mangrovei on Rhizophora mucronata from Karnataka mangroves. Maria et al. (2005) investigated the antimicrobial and enzymatic activities of endophytic fungi isolated from Acanthus ilicifolius and Acrostichum aureum from Nethravathi mangroves. Further studies on fungal diversity on decaying intertidal wood were conducted by Maria and Sridhar (2003) and Ghate and Sridhar (2015). Suryanarayanan and Kumaresan (2000), Kumaresen and Suryanarayanan (2002), Suryanarayanan (2012a,b) and Venkatachalam et al. (2015) documented the endophytes of various mangrove plants, sea sponges, sea grasses and marine macroalgae of southwest coast of India. Suryanarayanan et al. (2010) assessed the ability of endophytes to 246 K.-L. Pang et al.: Country reports of marine mycological research produce antialgal, antifungal, antibacterial, antiinsect, and antioxidant compounds. Raveendran and and Manimohan (2007) published a book entitled ‘Marine fungi of Kerala’, which covers 80 marine fungal species from the Kerala coast. Khan and Manimohan (2011) listed 23 marine fungi associated with driftwood from coastal sites in Kerala State and the Lakshadweep Islands of India. Nambiar and Raveendran (2009) examined the marine mycoflora across several coastal locations in Andhra Pradesh, Kerala, and Tamil Nadu, while Nambiar and Raveendran (2010) and Nambiar and Raveendran (2015) focused on the frequency and abundance of fungi on arenicolous marine and animal substrata, respectively. Samir Damare joined as a Scientist at the CSIR National Institute of Oceanography, Goa, India in 2009, and he currently works on diversity of deep-sea fungi and their biotechnological potential. Fungal growth in a simulated deep-sea environment was investigated using a proteomic technique by Krishnaswamy (2019). The highest number of mangrove fungi, 339, has been documented in India in studies compiled by Devadatha et al. (2021b). A total of seven novel genera and 44 species were described along the coasts of India. At present, the Department of Biotechnology, Pondicherry University and the National Institute of Oceanography in Goa, India are the only two institutions actively involved in marine fungal research. Marine fungal research, however, needs greater resources, including dedicated research facilities and personnel. Marine fungi are an integral part of India’s bioresources, and the country’s extensive coastline provides ample opportunities for exploration. 4.4 Malaysia (E.B.G. Jones) Marine fungi, especially those on mangrove substrata, have been extensively studied in Malaysia, resulting in the compilation of a monograph on Malaysian mangrove fungi (Alias and Jones 2009). Jones and Tan (1987) initiated the study of manglicolous marine fungi in Malaysia listing 32 species collected at Gelang Patah mangrove, Johor, while Jones and Kuthubutheen (1989) recorded 82 species from Morib, Kuala Selangor, Port Dickson and Sementa mangroves. Alias et al. (1995) listed 100 species of marine fungi (82 ascomycetes, 15 asexual fungi and three basidiomycetes) collected from three mangrove stands in Kuala Selangor, Morib and Port Dickson, while Alias and Jones (2000a,b) recorded 53 species of fungi associated with Rhizophora apiculata from Morib mangrove. Currently, 390 marine mangrove fungi are recorded from Malaysia (Alias et al. 2010). Investigations of marine fungi in Malaysia fall under several headings: systematics, generally supported by molecular data (Acrocordiopsis sphaerica, Alias et al. 1999; Calathella mangrovei, Jones and Agerer 1992; Corollospora besarispora, Sundari et al. 1996a; Fasciatispora lignicola, Alias et al. 1994; Phomatospora nypae, Hyde 1993b; Pyrenographa xylographoides, Alias et al. 1996; Tirisporella beccariana, Jones et al. 1996, and others); surveys of different substrata and locations (Alias and Jones 2009; Alias et al. 2010; Hyde 1993b; Hyde and Alias 2000; Jones and Alias 1996; Jones and Kuthubutheen 1989; Jones and Tan 1987; Kuthubutheen 1981; Pang et al. 2010b; Sundari et al. 1995, 1996a,b; Yanna et al. 2001; Zainuddin et al. 2008), production of antimicrobial compounds (Zainuddin et al. 2008, 2010), ultrastructure studies (TEM, SEM) (Alias et al. 2001; Yusoff et al. 1994a,b,c, 1995), and experimental studies (Alias and Jones 2010; Sundari and Vikineswary 2002). Several monographs have been published: ‘Marine fungi from mangroves of Malaysia’ by Alias and Jones (2009), ‘Checklist of fungi of Malaysia’ (Lee et al. 2012, includes marine fungi), ‘Malaysian fungal diversity’ (Jones et al. 2007, includes marine fungi). 4.5 Philippines (E.B.G. Jones and M. Calabon) Many published studies explore the marine fungi in the Philippines, the earliest by Kohlmeyer (1968) based on his single collection from Subic Bay of Antennospora quadricornuta observed from test panels of Dipterocarpus sp. and Pseudotsuya sp. Flor Uyenco was the guiding light for marine mycology in the Philippines and was the course leader of the innovative idea from UNESCO to provide funding for a six-week workshop on mangrove fungi at the University of the Philippines, Diliman campus, which supported one scientist from each Asian country, with lecturing staff that included C.V. Subramanian, Gareth Jones, and the publication of the presented papers (Agate et al. 1988). A number of the students went on to work in the subject (W.F. Leong, Singapore; J. Torres, Philippines; A. Chalermongse and T. Boonthavikoon, Thailand). Using sugarcane bagasse and rice straw as baits, Gacutan and Uyenco (1983) isolated Antennospora quadricornuta, Clavariopsis bulbosa, Halocyphina villosa, Nia vibrissa, Torpedospora radiata, Verruculina enalia and Lulworthia sp. in the Province of Aklan. Jones et al. (1988) recorded 31 manglicolous fungi (30 Ascomycota, 1 Basidomycota) from Pagbilao mangrove, Quezon. Most are Sordariomycetes (16 species), followed by Dothideomycetes (12 species), Eurotiomycetes (Sclerococcum haliotrephum), K.-L. Pang et al.: Country reports of marine mycological research and Leotiomycetes (Halenospora varia). Jones et al. (1996) introduced a novel genus Tirisporella typified by Tirisporella beccariana isolated from both the rachis of Nypa fruticans in Pampanga Province and the petioles in Quezon Province. Alias et al. (1999) studied marine fungi from mangrove driftwood and decayed wood attached to their host in three different sites (Boracay, Taklong, Pagbilao), and recorded 51 taxa including a novel species Acrocordiopsis sphaerica. In Siargao Island, Besitulo et al. (2010) identified 66 taxa with 46 new records for the Philippines. For the past decade, most researchers have focused on terrestrial fungi and there is still a large knowledge gap on the diversity of marine fungi in the Philippines. Other contributions to marine mycology in the country have been by: Thomas Edison Dela Cruz on antimicrobial, antioxidant activities and decoloration of dyes by marine fungi from mangrove material and seaweeds (Torres et al. 2012); Resurreccion B. Sadaba on marine fungal communities in bunker C oil-impacted sites off southern Guimaras, Philippines (Sadaba and Sarinas 2010). 4.6 Saudi Arabia (M.A. Abdel-Wahab and A.H. Bahkali) The first report of marine fungi from Saudi Arabia was by Aleem (1978) who reported two species: Corollospora pulchella and Okeanomyces cucullatus from driftwood samples collected along the Red Sea coast. Bokhary et al. (1992) recorded 37 fungal species from sea water and sea foam samples collected from the Arabian Gulf, of which 7 species were marine: Paradendryphiella salina, Nereiospora comata, Dictyosporium pelagicum, Ophiobolus australiensis, Papulaspora halima, Pontogeneia calospora and Okeanomyces cucullatus. Mohamed A. Abdel-Wahab joined King Saud University in 2011 where he carried out taxonomic and ecological studies on marine fungi and recently on thraustochytrids from mangroves along the coast of the Red Sea and the Arabian Gulf in Saudi Arabia. He supervised two master students (Mohamed S. Hodhod and Mohamed O. Al-Hebshi). Gareth Jones joined King Saud University in 2013 where he collaborated with Ali H. Bahkali through the Distinguished Scientist Fellowship Program (DSFP) and this collaboration is ongoing. These collaborative studies have resulted in several ecological, physiological and taxonomic studies with the introduction of 12 new species, four new genera and one new family (Abdel-Wahab et al. 2014, 2016, 2017, 2018, 2019a,b, 2020, 2021a,b,c, 2022; Ariyawansa et al. 2015; Hodhod et al. 2012; Hyde et al. 2016; Li et al. 2016; Liu et al. 2015). 247 Hodhod et al. (2012) conducted the first study of marine fungi from mangroves in Saudi Arabia. He collected decayed mangrove wood and leaf samples of Avicennia marina from two mangrove sites at Yanbu city in Saudi Arabia. He recorded 36 fungi (19 from decaying intertidal wood and 17 from decaying submerged leaves) of which 21 marine fungi (including 18 from wood and 3 from leaves) were new for Saudi Arabia. The recorded fungi included 7 new species, of which Amarenographium solium was published (Hodhod et al. 2012). Abdel-Wahab et al. (2014) recorded 37 marine fungi from 457 samples of driftwood and intertidal decayed wood of Avicennia marina collected from three sites along the Red Sea coast of Saudi Arabia. Most of the recorded fungi (31) were new records for Saudi Arabia. That study further documented marine fungi from the tropical mangroves at Al-Leith city along the coast of the Red Sea, Saudi Arabia. AlHebshi (2015) studied marine fungi from mangroves in the Arabian Gulf, Saudi Arabia for the first time. He recorded 19 species (11 ascomycetes and 8 asexual ascomycetes) from 60 samples of dead wood of Avicennia marina and driftwood that were collected from Tarut Island mangroves, Saudi Arabia. Of these 19 species, 14 were new records for Saudi Arabia and 9 were new to science, of which Halocryptovalsa avicenniae was formally described (Abdel-Wahab et al. 2017; Dayarathne et al. 2020b). Abdel-Wahab et al. (2021a) conducted high-throughput amplicon sequencing study of the mycobiome associated with leaves of the seagrass Halophila stipulacea collected from a mangrove site in Saudi Arabia. They sequenced the first 300 bp of the 28S rDNA amplicon using Illumina MiSeq (bTEFAP). Fungi represented between 1.1 % and 5.8 % of the total reads in the five samples. A total of 18,279 reads (representing 1.96 % of the total reads) were recorded from the five samples representing 296 molecular species (operational taxonomic units, OTUs) that belong to 13 fungal phyla. At the phylum level, Basidiomycota dominated the community (37.2–51.6 %) in three of the five samples, while Neocallimastigomycota (37.5 %) and Mucoromycota (42.1 %) dominated the community in the fourth and the fifth samples, respectively. 4.7 Taiwan (K.L. Pang) Early research on marine fungi/fungus-like organisms in Taiwan was on Halophytophthora, thraustochytrids and chytrids. Volz et al. (1976) isolated a number of species of the Thraustochytriaceae in coastal habitats of Taiwan, in conjunction with a few marine true chytrids, Chytridium chaetophilum, Diplochytridium citriforme, Rhizophydium sphaerotheca (Chytridiomycota) and Olpidium pendulum 248 K.-L. Pang et al.: Country reports of marine mycological research (Olpidiomycota). Chytridium lagenaria, Rhizophydium keratinophilum, Globomyces pollinis-pini and Paludomyces mangrovei were also documented from marine habitats of Taiwan (Chen 2020). Ho and Jong (1990) established the genus Halophytophthora and described H. kandeliae (now in Phytopythium) (Ho et al. 1991) and H. elongata (now in Salisapilia) from fallen mangrove leaves in Taiwan (Ho et al. 2003). SungYuan Hsieh (Bioresource Collection and Research Center, Hsinchu, Taiwan) obtained his PhD from the University of Portsmouth, UK on ultrastructure of marine fungi, especially arenicolous species (Hsieh et al. 2007). He documented 9 arenicolous marine fungi from Taiwan, including Arenariomyces spp., Carbosphaerella leptosphaerioides and Corollospora spp. (Hsieh 2002). In the same year, Hsieh et al. (2002) published a monograph of marine fungi from Taiwan and illustrated 59 species, predominantly Ascomycota. Research on marine fungi has been mainly undertaken by Ka-Lai Pang and his main collaborators Sung-Yuan Hsieh and Gareth Jones (King Saud University). In Taiwan, 107 species of Ascomycota, Basidiomycota and asexual fungi were recorded from coastal habitats (mangroves, sandy beaches, rocky shores) of Taiwan (Pang and Jheng 2012a), including many new species such as Kitesporella keelungensis (Pang and Jheng 2012a), Sedecimiella taiwanensis (Pang et al. 2010a), Pileomyces formosanus (Pang and Jheng 2012b) and Sclerococcum vrijmoediae (Pang et al. 2014). Pang et al. (2011b) published a monograph on the marine mangrove fungi of Taiwan, with full descriptions and illustrations. Currently, his research topics include the morphological and molecular diversity of marine fungi in coastal environments of Taiwan, and the ecology of fungi in a marine shallow-water hydrothermal vent at Kueishan Island, Taiwan. 4.8 Thailand (Mark S. Calabon and E.B. Gareth Jones) The first report of a marine fungus from Thailand was by Kohlmeyer (1984) who reported 15 species from the Chonburi area. Koch (1986) listed 16 species with two new marine fungi Arenariomyces parvulus and Corollospora cinnamomea. Hyde (1989), Hyde and Jones (1992), and Hyde et al. (1990) collected mangrove fungi from the Ranong and Phang Nga Provinces, and driftwood along shores at Phuket, and introduced the fungi: Astrosphaeriella mangrovei, Bathyascus grandisporus, and Hypophloeda rhizospora. Sakayaroj et al. (2004) listed 147 marine fungi from Thailand including three Basidiomycota, 117 Ascomycota and 26 asexual morphs. Research on marine fungi continued thereafter at BIOTEC (National Centre for Genetic Engineering and Biotechnology), Pathum Thani; Burapha University, Chonburi; and Mae Fah Luang University, Chiang Rai, Thailand, resulting in extensive additions to the marine mycology literature (see selected literature: Calabon et al. 2021; Dayarathne et al. 2017; Hattori et al. 2014; Hyde and Nakagiri 1989; Hyde et al. 1993; Jarikhuan 2002; Jones et al. 2017; Loilong et al. 2012; Pang et al. 2013; Pilantanapak et al. 2005; Suetrong et al. 2015, 2017; Supaphon et al. 2017; Unagul et al. 2017; Wijesinghe et al. 2023; Zhang et al. 2019). All these refer to the documentation of new taxa. Marine yeasts have been studied at Kasetsart University, Bangkok by Am-in et al. (2008) and Limtong et al. (2010) with many new taxa described from mangroves in Thailand. Another intensively researched topic in Thailand is secondary metabolite production from marine fungi at two centers: BIOTEC, Bangkok and Prince of Songkla University, Songkhla (selected literature: Chinworungsee et al. 2001; Isaka et al. 2002, 2010; Phongpaichit et al. 2006; Rukachaisirikul et al. 2009, 2011; Trisuwan et al. 2009, 2011). 5 Australasia 5.1 Australia (S.C. Fryar) The first record of a marine fungus in Australia was by Johnson and McNeil (1941) who recorded an unidentified ascomycete in hardwood immersed in seawater in Sydney. Cribb and Herbert (1954) reported three species of fungi parasitizing marine algae in Tasmania (Haloguignardia tumefaciens [as Guignardia tumefaciens], Massarina cystophorae [as Otthiella cystophorae], Chadefaudia gymnogongri), the first two were new species. Cribb and Cribb then went on to document 20 more marine fungi between 1955 and 1969 (Cribb and Cribb 1955, 1956, 1960, 1969), leading to the description of 10 new species. They were among the first in the world to study mangrove fungi. Following this, Jan Kohlmeyer and Brigitte VolkmannKohlmeyer expanded our knowledge of marine fungi in Australia, mostly with collections in Queensland (Kohlmeyer 1972, 1973a, 1984, 1986; Kohlmeyer and Volkmann-Kohlmeyer 1987, 1989, 1991). During the 1990s, Kevin Hyde added to the records (Hyde 1990, 1992b,c, 1995; Hyde and Nakagiri 1991), describing a number of new taxa including Tunicatispora australiensis (Hyde 1990), Cryptovalsa halosarceicola (Hyde 1993a), Eutypa bathurstensis (Hyde and Rappaz 1993), and Eutypella naqsii (Hyde 1995). Most of these studies were focused on fungi on mangrove wood and driftwood in Queensland, with some work also in New South Wales and Victoria. Abdel-Wahab and Jones (2000) reported three new species from driftwood collected from a sand dune at Mornington Peninsula Nature Park, Victoria, Australia: Caryospora australiensis, Platystomum scabridisporum and Savoryella melanospora. K.-L. Pang et al.: Country reports of marine mycological research A recent survey of fungi on mangrove wood in South Australia listed 43 marine fungal species (Fryar et al. 2020). Only one species, Corollospora maritima, had previously been found in South Australia and 11 had not previously been recorded in Australia. Also, in South Australia a new genus Annabella, was introduced from intertidal mangrove wood with one species Annabella australiensis (Fryar et al. 2019). Currently, there are 132 marine fungi recorded for Australia (https://freshwaterandmarinefungiaustralia.com/). Most of these records are from mangrove wood or pneumatophores. Although a range of other substrata have been investigated, such as live corals (Kendrick et al. 1982), macroalgae (Cribb and Cribb 1969), sand grains (Kohlmeyer and Volkmann-Kohlmeyer 1991), samphire (Hyde 1993a), and animal pathogens (Langdon and McDonald 1987; Norton et al. 1994), these records are rare. McCarthy (1991, 1994, 2001, 2008) reported a number of Verrucaria marine lichens from Australia, including the new species: V. alborimosa, V. coralliensis, V. meridionalis, V. australiensis, V. sessilis, and V. subdiscretia. Other species recorded from Australia include: Verrucaria mucosa, V. serpuloides, V. microsporoides, V. halizoa, V. aucklandica, V. prominula, V. striatula, V. subdiscreta, V. fusconigrescens and V. maura (McCarthy and Kantvilas 2015). To understand the ecology of marine fungi in Australia, their role and importance in marine habitats, there needs to be significantly more investment in baseline data. Most records of marine fungi in Australia are single records. We have little idea of the distribution of most species or the stability of their populations. These organisms are likely to be under significant threat from human activity and we currently have no way of knowing their conservation status. Australia has more than 34,000 km of coastline, many offshore islands, more than 1000 estuaries and hundreds of inland saltwater lakes. In other parts of the world seagrasses (Poli et al. 2022), deep-sea hydrothermal vents (Pang et al. 2019), microscopic invertebrates (Holt et al. 2022), sediments (Zhang et al. 2021) have been found to support high fungal diversity. In Australia, the vast majority of these habitats and substrata have not yet been explored for marine fungi. 6 Europe 6.1 France (G. Burgaud, L. Meslet-Cladière, M. Mehiri, J. Dupont, S. Prado and C. Roullier) Marine mycology in France started with the description of the first marine fungus, Leptosphaeria typharum (current 249 name Juncaceicola typharum) by Jean Baptiste Henri Joseph Desmazières (Desmazières 1849). Early marine mycology in France consisted of sporadic descriptions of marine fungal species by (i) the Crouan brothers in their “Florule du Finistère’’ which can be translated as the “Flora of the extreme west of Brittany” (Crouan and Crouan 1867), (ii) Feldmann (1957) describing the ascomycetous parasite Chadefaudia marina on the marine alga Palmaria palmata, and (iii) Doguet (1962) describing the basidiomycete Digitatispora marina on submerged wood in seawater. A total of 14 ascomycetous (Leptosphaeria typharum, Sphaeria posidoniae, Camarosporium roumeguerei, Thalassoascus tregoubovii, Chadefaudia marina, Asteromyces cruciatus, Diplocladiella scalaroides, Didymella magnei, Xylomyces rhizophorae, Nais inornata, Ceriosporopsis capillacea, Haloguignardia cystoseirae, Corollospora armoricana, Acremonium neocaledoniae) and three basidiomycetous (Mycaureola dilseae, Digitatispora marina, Flamingomyces ruppiae) taxa were described from France and French territories (French Guiana, Guadeloupe, Martinique, Mayotte, Réunion, French Polynesia, New Caledonia, etc.) during the period spanning 1849 to 2008. It should be noted that this list of 17 species is not exhaustive as it was obtained by cross-referencing the marinefungi.org and indexfungorum.org databases and some information was missing for certain taxa. This limited number of studies describing the marine fungal diversity in France and French territories indirectly highlights the unexplored reservoir of biodiversity in the very different and contrasted habitats spread in this vast and expanded country. For example, mangroves, lagoons, coral reefs of French overseas departments and territories, unique habitats of French Austral Lands and Seas, exploration of deep-sea and deep subseafloor habitats, etc. Marine mycology in France is currently conducted mainly by four laboratories using complementary approaches and thus working together on many research projects related to marine fungi. (i) ISOMer (“Institut des Substances et Organismes de la Mer”): Studies on marine fungi in Nantes began in the late 1990s at the instigation of Yves François Pouchus, who first hypothesized that fungi might explain some atypical episodes of seafood toxicity. Several samples in shellfish farming areas were then collected and allowed to build a collection of more than 1000 marine fungal strains from the Atlantic coast (Sallenave-Namont et al. 2000). These were then first investigated for mycotoxin production (Grovel et al. 2003; Landreau et al. 2002; Ruiz et al. 2007; Vansteelandt et al. 2012). Many families of compounds could then be identified from these fungal strains and led to more recent research, which aims at understanding their role in nature such as for 250 K.-L. Pang et al.: Country reports of marine mycological research communication or defense. The team has then gained expertise in mass spectrometry metabolomics and associated bioinformatics to decipher the impact of abiotic and biotic stresses on metabolite production from marine fungi. Media enriched with environmental samples (extracts from mussels, shrimps and sponges) as well as co-cultures (fungi-fungi, fungi-bacteria, fungimicroalgae) have been developed and are now used on a regular basis for all sorts of studies (Berry et al. 2023; Bertrand et al. 2017; Fernand et al. 2017; Hoang et al. 2018; Kerzaon et al. 2009; Roullier et al. 2016; Vansteelandt et al. 2013). In addition, the potential of marine fungi and fungal metabolites for biocontrol and drug discovery, particularly in the fight against cancer and infectious diseases, is also investigated (Dias et al. 2015; van Bohemen et al. 2021). Recent developments also include the assessment of marine fungal enzymes (more specifically vanadium-haloperoxidases) as new tools for biocatalysis and green chemistry (Cochereau et al. unpublished). Following an initial workshop in July 2014 in Prince Edward Island in Canada, the team hosted in Nantes the first international conference on Marine Fungal Natural Products (MaFNaP) in July 2015. It was a joint meeting with the 14th International Marine and Freshwater Mycology Symposium and was the first event of this type uniting both ecologists and chemists. (ii) The LUBEM, a research laboratory of the “Université de Brest, (UBO)”, began studying marine fungi in the early 2000s at the initiative of Georges Barbier, who hypothesized that fungi may occur in deep-sea habitats and more precisely in deep-sea hydrothermal vents. Having confirmed this hypothesis by highlighting fungal communities in such extreme habitats using culture-dependent and culture-independent methods with the help of several PhD students (Burgaud et al. 2009, 2010, 2011; Le Calvez et al. 2009), the research theme has then evolved towards the analysis of other habitats, either extreme, such as deep subsurface sediments (Ciobanu et al. 2014; Rédou et al. 2014), or non-extreme, such as coastal waters (Li et al. 2019; Wang et al. 2021). The team has acquired expertise in uncovering the diversity, activity and ecological roles of marine fungi by using a combination of approaches, i.e., metabarcoding, (meta)genomics, (meta) transcriptomics, metabolomics and high-throughput culturing technique. Recently, the LUBEM has implemented screening strategies to uncover the biotechnological potential of the hundreds of marine fungal isolates generated in the frame of numerous research projects and preserved in the UBO Culture Collection (https://nouveau.univ-brest.fr/ubocc/fr). These recent developments include the assessment of marine fungal enzymes involved in depolymerization of plastics (Burgaud et al. 2022; Philippe et al. 2023), degradation of hydrocarbons (Maamar et al. 2020), or more specifically vanadium-haloperoxidases as new tools for biocatalysis and green chemistry (Cochereau et al. 2022). (iii) The Marine Natural Products (MNP) team, led by Mohamed Mehiri, is a strong component of the Institute of Chemistry of Nice (ICN, UMR 7272 CNRS). Located at Université Côte d’Azur (UCA), the MNP team has a long tradition in the study of marine organisms, including marine fungi (Bovio et al. 2019a,b; Elsebai et al. 2018; Keeler et al. 2021; Marchese et al. 2020; Quémener et al. 2021). The research activity of the Natural Products group focuses on high value-added molecules isolated from diverse marine (micro)organisms with the aim to isolate and identify new bioactive compounds using the analytical facilities of the UCA (nHPLC, 2 NMR, HPLC-MS, MS L&H resolution) and an established network of collaborations, notably for screening. As leader of the MNP team, Mehiri has great experience in isolation, structural elucidation, synthesis and valorization of high value-added molecules. (iv) National Museum of Natural History (MNHN) has always had considerable expertise in mycology. The Museum’s collection of fungal strains currently contains more than 6,000 strains (including 350 types) corresponding to 1,425 different species (https://www. mnhn.fr/en/fungal-strain-collection). The collection is particularly focused on terrestrial ascomycetes and zygomycetes, but contains some specimens from marine and aquatic environments (Dupont et al. 2009; Samadi et al. 2010). Research on marine fungi has increased in recent years with the collaboration between the Chemistry of Fungal and Bacterial Natural Products (CPNFB) team of the Unit Molecules of Communication and Adaptation of Microorganisms (UMR 7245 MCAM) and the MNHN collection. Indeed, the CPNFB team is developing integrative and multiomics approaches, from the “gene to the molecule”, to decipher the molecular interactions between microbiota (bacteria and fungi) and macroalgae. In this context, endophytes and epiphytes associated with kelps (Fucales and Laminariales) were analyzed using cultivable and non-cultivable approaches along with the chemical characterization of their metabolites. These studies highlighted the key role of the chemical mediation in fungi-microbiota, fungi-pathogen and fungi-host interactions (Tourneroche et al. 2020; Vallet et al. 2018, 2020). These works have also generated a K.-L. Pang et al.: Country reports of marine mycological research collection of marine fungal strains (>500) along with a library of fungal crude extracts that are exploited in the frame of various national, European and international research projects for their biosynthetic potential, ecological role and potential uses (Dezaire et al. 2020). Today, marine mycology is a key theme of CPNFB projects and its study should open new avenues on the ecological role of fungi in the marine holobiont. 6.2 Germany (T. Rämä and M. Reich) Germany has long traditions in the studies of marine fungi and several of the pioneering researchers in the field were German. The studies made during the 20th century focused on the taxonomy, geographical and vertical distribution within the sublittoral-tidal zone and physiology of marine fungi, whereas current research focuses on molecular biosystematics, the roles and importance of marine fungi in biogeochemical processes and natural products discovery. In 1922, Erich Werdermann, the curator of the mycological collections in Berlin-Dahlem, described perhaps the most iconic marine fungus Corollospora maritima (Werdermann 1922). Willy Höhnk at the Institut für Meeresforschung in Bremerhaven studied the occurrence and taxonomy of marine fungi (Höhnk 1955). Through these studies he became convinced of the distinct nature of fungi in saline waters that legitimized the existence of marine mycology as an independent research field, and initiated the first International Marine (and later Freshwater) Mycology Symposium (IMMS) in Bremerhaven in 1966. Karsten Schaumann continued research on marine fungi in Bremerhaven with special interest in their growth and enzyme production. He isolated fungi from German and foreign waters, from the subtropics to the polar regions, thereby establishing the KMPB (Kulturensammlung Mariner Pilze Bremerhaven) collection (Schaumann 1968). Other studies at the Institut für Meeresforschung include marine and mangrove chytrids (Ulken 1970, 1972) and quantitative estimation of thraustochytrids in sea water and their taxonomy (Gaertner 1980, 1982). Zuccaro et al. (2008) investigated marine fungi associated with the brown seaweed Fucus serratus and their identification. Physiological studies of marine fungi, their reproduction and tolerance of hydrostatic pressure were conducted by Molitoris and his research team at Regensburg University (Lorenz and Molitoris 1997). At the same time, Ingeborg Schmidt conducted an extensive study on marine fungi along the German Baltic coast (Schmidt 1974). The renowned Jan Kohlmeyer started his career in Germany, with biodeterioration studies of fungi 251 in marine wood at the Bundesanstalt für Materialprüfung in Berlin-Dahlem, but continued his career, which resulted in the description of hundreds of new taxa (Kohlmeyer and Kohlmeyer 1979) and later Kohlmeyer and VolkmannKohlmeyer (2001), as professor at the University of North Carolina, USA. Currently active German marine mycologists include Marlis Reich (University of Bremen) who is developing molecular toolkits for the taxonomic classification and detection of marine fungi in environmental samples (Priest et al. 2021) and studies of marine fungal diversity (Yang et al. 2021). Additionally, she is interested in the carbon turnover of marine fungi, and recently isolated hundreds of marine fungi to establish model organisms. Hans Peter Grossart in Stechlin has been working on the biological aspects of the aquatic carbon cycle since his PhD in Constance, initially with a main focus in bacteria, but increasingly also fungi. Even though most of his work is carried out in freshwater systems, many of his results and concepts are equally valid for marine systems, such as the concept of mycoflux, mycoloop, and fungal shunt that describe the ecological roles fungi play in aquatic carbon turnover and food chains (Grossart et al. 2019; Klawonn et al. 2021). A former doctoral student of Grossart, Christian Wurzbacher (Technical University of Munich), investigates unknown fungi in aquatic biofilms, and established Oxford Nanopore Sequencing for aquatic fungi (Wurzbacher et al. 2018). Noteworthy is also William Orsi (Ludwig Maximilian University of Munich) who works on the effects of benthic microbial diversity on biogeochemical processes. Using omics and stable-isotope probing techniques, he defined a specialized role of fungi in carbohydrate recycling in the seafloor, distinct from Bacteria and Archaea (Orsi et al. 2018), and showed that marine fungi can assimilate similar amounts of carbon as bacteria (Orsi et al. 2022). Johann F. Imhoff, former professor for Marine Microbiology at the “Institut für Meereskunde” in Kiel (now GEOMAR), sustainably established the discovery of natural products of marine microbes in science and politics in Germany. In 2000s, he took over the KMPB collection, was able to draw from it a large spectrum of new secondary metabolites for various applications demonstrating the great potential of culture collections for natural product mining (Imhoff 2016). Imhoff retired in 2014 and was succeeded by Deniz Tasdemir. Tasdemir has been increasingly successful in using co-cultivation to isolate new secondary metabolites from marine fungi through interaction-dependent activation (Oppong-Danquah et al. 2018). Antje Labes (Flensburg University of Applied Sciences), a former colleague of Imhoff and Tasdemir, focused in her newest research in 252 K.-L. Pang et al.: Country reports of marine mycological research mycoremediation using marine fungi. She has accommodated a large part of the KMPB collection with about 16,000 previously unused isolates (pers. comm.) at the Flensburg strain collection of marine fungi. Frank Kempken (Christian Albrechts University in Kiel) has been working since 2001, focusing on plant and terrestrial fungi. In recent years, however, he is using his expertise to obtain information about biosynthetic gene clusters from genome sequences of marine fungi and thus deduce potential biotechnological applications (Kumar et al. 2018). The number of marine fungi documented in Germany has not been summarized in recent decades. However, it can be estimated that there are about 20,000 marine fungal isolates in existing culture collections. Molecular work in German marine waters predicts several thousand species (Banos et al. 2020). 6.3 Italy (E.B.G. Jones) In the early 1980s the seeds of marine mycology research were initiated by Vincenzo Cuomo who was working at Ciba Geigy at their plant in Torre Annunziata, as the company was interested in seeking new bioactive compounds from marine fungi. Cuomo was registered for his PhD at the University of Portsmouth and published a number of papers about marine fungi on the seagrasses Posidonia oceanica and Cymodoce nodosa (Cuomo et al. 1985, 1988) and on marine algae (Cuomo et al. 1983). In a joint paper (Jones et al. 1983) he described spore appendage development in the lignicolous marine pyrenomycetes Marinokulati chaetosa and Halosarpheia trullifera. These early studies lead to the discovery of new secondary metabolites by Francesco Pietra and his group (University of Trento), especially dendryphiellin A, the first fungal trinor-eremophilane isolated from the marine fungus Paradendryphiella salina (Guerriero et al. 1988). Subsequently, other eremophilanes were elucidated by this group (Guerriero et al. 1989). Also at this time, marine fungi were studied at the University of Messina, where Sofia Grasso was working on her PhD documenting fungi found in the local harbors (Bruni et al. 1982; Grasso et al. 1985, 1990). C. Panebianco, undertook her PhD at Messina, with practical work at the University of Portsmouth on the physiology of marine fungi (Panebianco 1990) and experimental work on the sequential colonization of wood in the sea (Panebianco et al. 2002). During this period, Montemartini Corte (1975, 1979) also contributed to our knowledge on the marine fungi of Italy with particular interest in the decay of wood in the marine environment. Italy also took part in an international co-operative research programme (OECD) into the biodeterioration of wood in the sea, leading to a number of publications (Jones et al. 1972, 1976). Jones (2010) published a list of marine fungi reported from Italian seas documenting 42 species, as part of a checklist of the flora and fauna. The next generation of marine mycologists came from the University of Turin where their work focused on marine fungi colonizing or endophytic on the seagrass Posidonia oceanica, but their first account documented asexual morphs best described as marine derived (Panno et al. 2013). These studies continued with observations of marine fungi on algae (Garzoli et al. 2014, 2018; Gnavi et al. 2017; Poli et al. 2020), Posidonia oceanica (Gnavi et al. 2014), woody substrata (Garzoli et al. 2015), oil spills (Bovio et al. 2017), and marine sponges (Bovio et al. 2019b). Many new fungal taxa were described from P. oceanica: the new genus Elbamycella with E. rosea as the type species (Juncigenaceae, Torpedosporales; Poli et al. 2019), Corollospora mediterranea (Halosphaeriaceae; Poli et al. 2021a,b) and Paralulworthia (Lulworthiaceae, Lulworthiales; Poli et al. 2019, 2022). These contributions are summarised in their recent publication (Poli et al. 2022) covering fungi on seagrasses, seaweeds and plant debris. 6.4 Norway (T. Rämä) Marine mycology is a young field of science in Norway. In the 19th and 20th centuries, a few marine fungal observations were made by mostly foreign mycologists during short visits to the country or based on exported material (summarized in Rämä et al. 2014a,b). These studies focused on studying wood substrata and seaweeds, but also fungi pathogenic in aquaculture and resulted in species described as new for science (e.g., Kohlmeyer 1973b; Pang et al. 2008, 2009; Pedersen and Langvad 1989), giving first indications that the Norwegian coastline is rich in fungal life. Systematic studies on Norwegian marine fungi were started by Teppo Rämä during his PhD studies in 2010–2014 that was initiated by Geir Mathiassen and Ove E. Eriksson from Umeå, Sweden. Eriksson had collected marine fungi in Norway and suggested Rämä to start studying these. Rämä´s thesis focused on studying the diversity and ecology of wood-inhabiting fungi in the North of the country, whereas marine fungal research has expanded to other research avenues in recent years. However, the geographical focus has been in Northern and Arctic waters, since marine mycologists have been based at UiT (The Arctic University of Norway, Tromsø at 71°N). Norwegian research on marine fungi was strengthened by Brandon Hassett who moved to Tromsø from Alaska, USA in 2017. Hassett stayed in Norway for some years and his postdoctoral research focused on the ecology of Arctic K.-L. Pang et al.: Country reports of marine mycological research marine fungi, especially chytridiomycetes, and other protists. Other persons involved in marine fungal research in Norway include Ole Christian Hagestad who defended his PhD thesis on bioprospecting of Arctic marine fungi in April 2021. Hagestad´s thesis involved culturing work and genome sequencing of promising fungal isolates to reveal their biosynthetic potential to produce new and interesting secondary metabolites. Rämä´s work as a postdoc and associate professor has continued characterizing the species diversity and expanding the culture collection of Arctic marine fungi while contributing with fungal isolates to the biodiscovery work done in the research group Marbio and Centre for New Antibacterial Strategies at UiT. The main research trends in Norwegian research on marine fungi have been in biosystematics, ecology and bioprospecting for antibacterial secondary metabolites using both traditional microscopy, culturing and bioassay, as well as -omics methods. The work has contributed to increased knowledge of the ecological importance of marine fungi and characterization of the new biological and chemical diversity of fungi in Arctic waters. Rämä et al. (2014a,b) provide a list of 61 species of marine fungi (60 ascomycetes and one basidiomycete) documented in Norway. DNA-based methods have revealed a much greater diversity but with uncertainties related to the molecular identification of fungi. Recent morphological work and the Norwegian marine fungi project (2022–2025) funded by the Norwegian Biodiversity Information Centre has already revealed several new species for Norway that is likely to bring the number of morphologically identified Norwegian species of marine fungi into the hundreds. 6.5 Portugal (E. Azevedo, M.F. Caeiro, A. Alves and M. Barata) Marine mycology in Portugal started in 1992 with the PhD work of Margarida Barata at the University of Lisbon (FCUL). The study involved the salt marshes of three rivers (Tejo, Sado and Mira) located on the west coast of Portugal and was the first report of marine fungi associated with Spartina maritima plants. This study contributed to knowledge of the vertical distribution of marine fungi in intertidal environments, as well as the recognition of the succession pattern of the marine fungi associated with S. maritima baits, placed for this purpose in the marsh of Mira River. Gareth Jones played a key role as a scientific consultant in this doctoral work, since he visited Portugal in 1993 and introduced the baiting method, essential for the detection of marine fungi on selected substrata. He helped to confirm the identification of a new basidiomycete associated with baits permanently 253 submerged in waters of the Mira River, Nia globispora (Barata et al. 1997). The work resulted in the publication of a book chapter (Barata 2002) and two scientific articles (Barata 2006; Barata et al. 1997). Margarida Barata was the supervisor of one MSc and two PhD theses. The MSc thesis of Dulce Figueira targeted the marine fungi associated with drifting substrata (wood and plant stems) collected in the intertidal zone of two beaches (Rosário and Guincho) located in the Sintra-Cascais area (Figueira and Barata 2007). Egídia Azevedo obtained a PhD degree in 2012, mainly addressing the occurrence, diversity, and similarity of marine mycota detected in Fagus sylvatica and Pinus pinaster baits submerged for a 1-year period in two marinas (Cascais and Sesimbra; Azevedo et al. 2010, 2011). This PhD project also included an inventory of the marine fungal communities associated with five categories of drift substrata (driftwood, Arundo donax, Phragmites australis, Spartina maritima, and other plant stems) randomly collected at four sandy beaches (Vagueira, Meco, Cascais and Vila Nova de Mil Fontes), leading to the proposal of a new sampling methodology to assess the representative marine mycota on drift substrata (Azevedo et al. 2012). This project was also the starting point, under the supervision of Maria F. Caeiro (FCUL), for the application of molecular techniques for fungal identification, the first publication addressing the molecular identification of isolates of asexual morphs not morphologically identified to species level (Azevedo et al. 2011). This approach, based on rRNA gene sequences, was also applied to establish phylogenetic relationships among isolates belonging to the genus Lulworthia, and the new taxon Lulworthia atlantica (Azevedo et al. 2017). Later, phylogenetic analysis associated with the estimation of pairwise distances was applied to evaluate the Nia vibrissa species complex (Azevedo et al. 2018). The PhD of Maria da Luz Calado concluded in 2016 and focused on Spartina maritima plants collected in two salt marshes: Ria de Aveiro (west north coast) and Castro Marim, Ria Formosa (south coast). This study provided an inventory of the filamentous higher marine fungi associated with this host plant, giving a better understanding of the ecology and functional roles of those fungi in the early stages of decomposition of S. maritima, also contributing to the evaluation of the effects of seasonality and environmental parameters on fungal communities (Calado et al. 2015). The molecular approach allowed either confirmation of fungi previously identified by morphological characteristics, or identification of additional fungal species only detected by this methodology (Calado et al. 2019). After her graduation, Calado et al. (2021) screened the endophytic fungi associated with the seaweed Halophteris 254 K.-L. Pang et al.: Country reports of marine mycological research scoparia for secondary metabolites with potential dermocosmetic applications. In 2021, Pedro Correia successfully completed his MSc thesis under the supervision of Egídia Azevedo and Maria F. Caeiro. This work aimed to characterize and evaluate the diversity of the Corollospora maritima sensu lato found in Portugal, and was extended to the molecular relationships between the species of the genus Corollospora, with published molecular data. Sridhar et al. (2012), while visiting Portugal, carried out a survey on seven sandy beaches on the north and central regions of west Portugal, with collections of driftwood and seaweeds, to study the occurrence, diversity and similarity of the marine fungi detected in these substrata and environments. By using direct observation of fungal morphology, Margarida Barata’s team and Sridhar et al. (2012) identified a total of 98 species of marine fungi (62 Ascomycota, five Basidiomycota and 31 asexual ascomycetes). Artur Alves group at CESAM and the University of Aveiro started working on fungi from marine environments in 2017. Since then, one PhD (Micael Gonçalves) and two MSc (Alberto Abreu, Tânia Vicente) are complete, and two PhD projects are ongoing. The overall aim of these studies is to unravel the diversity and biotechnological potential of fungi from marine environments. Strains were isolated from seawater, algae, saltmarsh plants, driftwood, submerged wood baits and sponges. Through morphological and molecular characterization (including multilocus phylogenies), more than 240 species were identified. This led to the description of 18 novel species, from 12 different genera, including some strictly marine, such as Zalerion pseudomaritima (Gonçalves et al. 2021a). A new genus, Neptunomyces, isolated from marine algae, was also described (Gonçalves et al. 2019). Gonçalves et al. (2021b) screened a collection of fungal isolates (marine-derived and strictly marine) for their ability to produce diverse extracellular enzymatic activities. Mycelial and medium extracts were also screened for antimicrobial, antioxidant, and cytotoxic activities. The genome and metabolome of Emericellopsis cladophorae, a new species from marine algae (Gonçalves et al. 2020), were analysed to gain knowledge on the biology and ecology of this fungus, and marine fungi in general, and to determine the biosynthetic potential of the species (Gonçalves et al. 2022). 6.6 Sweden (S. Tibell and L. Tibell) Carl A. Agardh, in his Syn. Alg. Scand. (Agardh 1817), included Lichina, with the marine lichen and generic type Lichina pygmaea. Elias Fries described many species, but none of them marine, although Patellaria atrata, type of Patellaria, was sanctioned in his Systema 2 (Fries 1822). Fries also described Vibrissea, which includes V. nypicola, a marine species. Although systematic mycology in Sweden, as built on the founding works of Elias Fries, remained strong in the 19th and 20th centuries, interest in marine fungi remained scant and fragmentary. Johanson (1884) described Mycosphaerella which later was to include numerous species (e.g. the marine Mycophycias ascophylli). The next note on a marine fungus did not appear until Starbäck (1896) reported Lizonia halophila as Sphaerulina halophila. Juel (1901) described Pyrrhosorus in the Labyrinthulales – at that time considered a fungus. An early 20th century report was provided by Cotton (1909), when describing Mycosphaerella ascophylli (now Stigmidium ascophylli) in Sweden (west coast). Nannfeldt, in his influential ‘Studien’ (1932), described Laetinaevia, and subsequently Orbilia marina was transferred to this genus (Kirk and Spooner 1984), so as to eventually end up in Calycina (Calycina marina). In his 1957 thesis, Lennart Holm reported Leptosphaeria littoralis and combined it into Phaeosphaeria. Similarly, Nils Lundquist described Tripterospora latipes (Lundquist 1969), the basionym for Zopfiella latipes. Rolf Santesson, an eminent lichenologist, had many-faceted interests and collected marine fungi on the Swedish west coast in the 1950s, collections that still remain mostly unrevised and kept in Uppsala. A pioneering, but neglected work, is the thesis by Erneholm (1972, in Swedish), where the author presented the methodology for studying and cultivating marine fungi. The investigations were focused on marine fungi occurring on algae from the Swedish West Coast and Kenya. The thesis also included discussions of the ecology of marine fungi and generally aimed to introduce marine mycology in Sweden. It remained unpublished, however, and the results were overlooked, although to some extent referred to by Henningsson (1974). Erneholm reported 12 ‘deuteromycete’ species from Sweden. Niels Fries, professor of physiological botany in Uppsala, initiated another line of research insofar that he concentrated on the physiology of marine fungi. Fries recruited PhD students for their study, Ulla Gustafsson being one of them (Fries 1965; Gustafsson and Fries 1956; Pedersen and Fries 1977). In the first of these papers, 10 marine ascomycetes were cultivated from material collected by Santesson. In a subsequent study, Fries (1979) described the physiology of an ‘algal endophyte’, viz. Stigmidium ascophylli. In another paper Fries and Thorén-Tolling (1978) reported on the endosymbiotic relationship between Stigmidium ascophylli and its host and identified the endophytic mycelium by antibody techniques. Here the term ‘endosymbiotic’ was used for a relationship involving a marine fungus for the K.-L. Pang et al.: Country reports of marine mycological research first time. The material used by Fries and his students was mainly obtained from wooden panels submersed at Kristineberg (now the Sven Lovén Centre, Sweden) collected by Santesson and the material identified by him. Henningsson, another pupil of Nils Fries, initially studied wood degradation and the physiology of marine fungi (Henningsson 1976a,b) and her thesis also included a first census of marine fungi of Sweden (Henningsson 1974) focusing on lignicolous species. The material was partly obtained from three different areas with different salinities along the Swedish coasts, including the Baltic, and 34 species were recorded. Birgitta Norkrans, yet another researcher who under Niels Fries’ leadership devoted herself to marine fungi and particularly their physiology, examined the physiological requirements of marine yeasts. Norkrans published on marine yeasts (Lundström-Eriksson and Norkrans 1968) and also described a new species, Candida suecica. Sven Nilsson in his thesis (Nilsson 1964) treated freshwater aquatic fungi of Sweden and in a later paper (Nilsson 1971) described Clavatospora, a genus later to accommodate C. bulbosa, the anamorph of Corollospora pulchella. In his thesis, Ove Eriksson (1981) described Amarenomyces based on A. ammophilae and also later continued to study marine/ shoreline fungi (Eriksson 1964, 1973, 1982; Kohlmeyer et al. 1995a,b,c, 1996, 1997, 1998). He meticulously included them in his checklist of non-lichenized ascomycetes of Sweden (2014), which also incorporated numbers from Fungi exsiccate suecici as published in Thunbergia volumes (Fasc. 26, 75). In addition, he referred to several of the Santesson collections of marine fungi. The precursor of the 2014 list (Eriksson 1992) also contained information on marine fungi. The international upsurge of interest in marine fungi during the late 20th century also impacted on Sweden, and a semi-popular review paper was published by Tibell (2016). Here, seven species previously unknown from Sweden were presented, two of them new to science (based on Santesson’s collection). This was part of a pilot-project funded by the Swedish Taxonomy Initiative in 2016. A crucial aspect of finding new material was a ‘kick-off’ meeting and joint fieldwork with E.B. Gareth Jones from the UK, and Ka-Lai Pang from Taiwan in June 2017 at the Sven Lovén Centre. The first outcome of the project 2018–2020 (financed by ‘ArtDatabanken’) was a compilation of previous records with substantial updates (Tibell et al. 2019) offering a census of Swedish species now amounting to 74, roughly doubling the number of species previously known from the country. The project was much indebted to the mentorship offered by Gareth Jones and Ka-Lai Pang, who both also joined in fieldwork on the Swedish east coast in 2019. Another contribution followed, including the description of a new species from Sweden, Coniochaeta marina (Jones et al. 2020). A review of the marine fungi of the Baltic (Tibell et al. 2020) 255 enumerated 77 species, where historical records were supplemented by the results of joint fieldwork in 2019. Thirteen species were reported new to Sweden. Further material collecting, axenic culturing and DNA sequence production followed until the project was discontinued due to lack of funding. 6.7 United Kingdom (E.B. Gareth Jones) Marine fungi have been extensively studied in the UK with observations from England, Ireland, Scotland and Wales. Sutherland (1915, 1916) undertook the first serious studies of marine fungi on various substrata, introducing the new genus Lulworthia on the brown alga Fucus and a number of new species: Cercospora salina, (=Paradendryphiella salina), and the doubtful species: Ophiobolus laminariae, Pleospora laminariana, P. pelvetiae, Rosellinia laminariana and Stigmatea pelvetiae. This was followed by the introduction of new taxa by Wilson (1954, 1956): Ceriosporopsis cambrensis, Halophiolobus purpurea (=Lulworthia purpurea), Halophiolobus rufus (=Lulworthia rufus) and the new genus Lindra (type species L. inflata). Studies by other British mycologists include: E.B. Gareth Jones, with circa 30 graduate students in marine mycology (systematics, wood decay, ultrastructure, ecology, physiology, phylogenetic studies, drug discovery); D.H. Jennings and his students (fungal physiology); D.J. Alderman (oyster diseases, thraustochytrids); R.A. Eaton (wood decay); S.T. Moss (ultrastructure of Ascomycota and Thraustochytrium species, Trichomycetes); G.J.F. Pugh (fungi in marine sediments, Antarctic marine fungi); L.V. Evans (fungal symbioses in marine algae); P. Curran (ecology and systematics marine fungi); and J.L. Polglase (mycotic infections of marine animals). The culture collection of marine fungi at the University of Portsmouth, comprising over 7,000 strains, including type strains, was lost through neglect on the departure of E.B.G. Jones. Key events: hosting two meetings of IMMS; edited volume by S.T. Moss ‘The Biology of marine fungi’ and checklists of marine fungi (Jones et al. 2009, 2015, 2019). Current research on marine fungi in the UK continues at the Plymouth laboratory of the Marine Biological Association U.K. with a major government project on plastic in the marine environment (Cunliffe 2023). 7 Conclusions Currently active marine mycologists have written briefly on the history and current state of marine fungal research of 20 different countries, highlighting their research interests and strengths. This is in the hope that such a paper will stimulate 256 K.-L. Pang et al.: Country reports of marine mycological research international and transdisciplinary research collaborations in marine mycology. What are the topics that marine mycologists will tackle in the forthcoming decades? (1) Few genomes of marine fungi have been sequenced and this has to be a priority area for the future (Amylocarpus encephaloides, Calycina marina, Corollospora maritima, and others). These will be important as a source of biosynthetic data that will provide information on the metabolic diversity of marine fungi, multilocus information for phylogenetic characterisation, a better resolution of their taxonomy, and comparative data on the evolution of individual genes (Galagan et al. 2005; Hagestad et al. 2021). (2) With the recent signing of a global diversity agreement for the conservation of the oceans, it is timely that marine mycologists play a greater role in the promotion of conservation, and examine the risk of extinction of marine fungi in response to climate change. (3) Future research should include a greater effort to determine the hidden diversity of basal lineages (e.g. Aphelidiomycota, Chytridiomycota, Rozellomycota), especially in global locations for which there are currently little data, including Africa, South America and Australasia (Jones 2011). (4) Greater effort is required to confront the pollution of the oceans by plastics and to educate the public about the fragility of the marine ecosystem. Many studies are in progress to determine the role of marine fungi in the breakdown of plastics, and also to evaluate how this information can be applied in the marine mileu (Cunliffe 2023; Ekanayake et al. 2022). Research funding opportunities, for example Biodiversa, are available for international consortia to apply to, and these may bring marine mycologists together to tackle these topics. Workshops/conferences (in-person/virtual) may serve as platforms for communication between marine mycologists, especially the new wave of young marine mycologists. For example, the International Marine and Freshwater Mycology Symposium has been held every 2–4 years since 1966, and was last held in 2019 in Xiamen, China. A special issue was published in Botanica Marina summarizing the contributions in this meeting (Pang et al. 2020), and the current article, as well as this new special issue, aims to encourage a more focused effort, bringing together scientists with different backgrounds in marine mycology. Acknowledgments: The authors would like to thank Dr. Paul M. Kirk for his assistance in cross-referencing the marinefungi.org and the indexfungorum.org databases. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission. Research funding: Ka-Lai Pang thanks the National Science and Technology Council, Taiwan for financial support (111– 2621–M–019–002–, 111–2621–B–019–001–MY3). Gareth Jones acknowledges the award of a Distinguished Scientist Fellowship (DSFP), King Saud University, Kingdom of Saudi Arabia. Gaëtan Burgaud acknowledges funding from the French National Research Agency grant ANR-19-CE04-000101 (MycoPLAST). Conflict of interest statement: The authors declare that they have no conflicts of interest regarding this article. References Abdel-Aziz, F.A. (2004). Biodiversity of aquatic fungi from the River Nile to the Sea, Ph.D. thesis. Sohag, South Valley University. Abdel-Aziz, F.A. (2008). Diversity of aquatic fungi on Phragmites australis at. Lake Manzala, Egypt. Sydowia 60: 1–14. Abdel-Aziz, F.A. (2010). Marine fungi from two sandy Mediterranean beaches on the Egyptian north coast. Bot. Mar. 53: 283–289. Abdel-Wahab, M.A. (2000). Diversity of fungi in subtropical mangroves. Ph.D. thesis. Sohag, South Valley University. Abdel-Wahab, M.A. (2005). Diversity of marine fungi from Egyptian Red Sea mangroves. Bot. Mar. 48: 348–355. Abdel-Wahab, M.A. and Jones, E.B.G. (2000). Three new marine ascomycetes from driftwood in Australian sand dunes. Mycoscience 41: 379–388. Abdel-Wahab, M.A., El-Sharouney, H.M., and Jones, E.B.G. (2001a). Two new intertidal lignicolous Swampomyces species from Red Sea mangroves in Egypt. Fungal Divers. 8: 35–40. Abdel-Wahab, M.A., Pang, K.L., El-Sharouney, H.M., and Jones, E.B.G. (2001b). Halosarpheia unicellularis sp. nov., (Halosphaeriales, Ascomycota) based on morphological and molecular evidence. Mycoscience 42: 255–260. Abdel-Wahab, M.A., Nagahama, T., and Abdel-Aziz, F.A. (2009). Two new Corollospora species and one new anamorph based on morphological and molecular data. Mycoscience 50: 147–155. Abdel-Wahab, M.A., Pang, K.L., Nagahama, T., Abdel-Aziz, F.A., and Jones, E.B.G. (2010). Phylogenetic evaluation of anamorphic species of Cirrenalia and Cumulospora with the description of eight new genera and four new species. Mycol. Prog. 9: 537–558. Abdel-Wahab, M.A., Hodhod, M.S., Bahkali, A.H.A., and Jones, E.B.G. (2014). Marine fungi of Saudi Arabia. Bot. Mar. 57: 323–335. Abdel-Wahab, M.A., Bahkali, A.H., Jones, E.B.G., Elgorban, A.M., Abdel-Aziz, F.A., Hodhod, M.S., and Al-Hebshi, M.O. (2016). Two new species of Kallichroma (Bionectriaceae, Hypocreales) from Saudi Arabian mangroves. Phytotaxa 260: 66–74. Abdel-Wahab, M.A., Dayarathne, D.C., Suetrong, S., Guo, S.Y., Alias, S.A., Bahkali, A.H., Nagahama, T., Elgorban, A.M., Abdel-Aziz, F.A., Hodhod, M.S., et al. (2017). New saprobic marine fungi and a new combination. Bot. Mar. 60: 469–488. Abdel-Wahab, M.A., El-Samawaty, A.M., El Gorban, A.M., Yassin, M.A., and Alsaadi, M.H. (2018). Khaleijomyces marinus gen. et sp. nov. K.-L. Pang et al.: Country reports of marine mycological research (Juncigenaceae, Torpedosporales) a new lignicolous marine fungus from Saudi Arabia. Phytotaxa 340: 277–285. Abdel-Wahab, M.A., Jones, E.B.G., Abdel-Aziz, F.A., and Bahkali, A.H. (2019a). Nia lenicarpa sp. nov. (Niaceae, Agaricales) from Red Sea mangroves in Saudi Arabia with comments on Nia vibrissa. Phytotaxa 406: 157–168. Abdel-Wahab, M.A., Jones, E.B.G., Bahkali, A.H., and El-Gorban, A.M. (2019b). Marine fungi from Red Sea mangroves in Saudi Arabia with Fulvocentrum rubrum sp. nov. (Torpedosporales, Ascomycota). Nova Hedwigia 108: 365–377. Abdel-Wahab, M.A., Jones, E.B.G., and Bahkali, A.H. (2020). Marine fungi recorded from Avicennia marina (Forsk.) Vierh. and their secondary product potential. Nova Hedwigia 111: 357–390. Abdel-Wahab, M.A., Bahkali, A.H., Elgorban, A.M., and Jones, E.B.G. (2021a). High-throughput amplicon sequencing of fungi and microbial eukaryotes associated with the seagrass Halophila stipulacea (Forssk.) Asch. from Al-Leith mangroves, Saudi Arabia. Mycol. Prog. 20: 1365–1381. Abdel-Wahab, M.A., El-Samawaty, A.M.A., Elgorban, A.M., and Bahkali, A.H. (2021b). Fatty acid production of thraustochytrids from Saudi Arabian mangroves. Saudi J. Biol. Sci. 28: 855–864. Abdel-Wahab, M.A., El-Samawaty, A.M.A., Elgorban, A.M., and Bahkali, A.H. (2021c). Thraustochytrids from the Red Sea mangroves in Saudi Arabia and their abilities to produce docosahexaenoic acid. Bot. Mar. 64: 489–501. Agardh, C.A. (1817). Synopsis algarum Scandinaviae 1817. Lundae: Ex officina Berlingiana. Agate, A.D., Subramanian, C.V., and Vannucci, M. (Eds.) (1988). Mangrove microbiology: role of microorganisms in nutrient cycling of mangrove soils and waters. United Nations Development Programme and UNESCO, New Delhi. Aleem, A.A. (1950a). A fungus in Ectocarpus granulosus C. Agardh near Plymouth. Nature 165: 119–120. Aleem, A.A. (1950b). Phycomycetes marins de diatomees et d’algues dans la region de Banyuls-sur-Mer (Pyrenees-Orientales). Vie et Milieu 1: 421–440. Aleem, A.A. (1950c). Phycomycetes marins parasites de diatomees et d’algues. Comptes Rendus Hebdomadaires des Seances de l’Academie des Sciences 231: 713–721. Aleem, A.A. (1952a). Marine fungi from the west coast of Sweden. Arkiv för botanik 2: 1–31. Aleem, A.A. (1952b). Olpidiopsis feldmanni sp. nov. champignon marin parasite d’algues de la famille des Bonnemaisoniacees. Comptes Rendus Hebdomadaires des Seances de l’Academie des Sciences 235: 1250–1252. Aleem, A.A. (1952c). Sur la présence de Melanopsamma tregoubovii Ollivier (Pyrénomycète) dans la Manche Occidentales. Parasite de Dilophus fasciola (Roth) Howe. Bulletin du Laboratoire Maritime de Dinard 36: 21–24. Aleem, A.A. (1953). Marine fungi from the west-coast of Sweden. Arkiv för Botanik 3: 1–33. Aleem, A.A. (1962). Marine fungi from the white sea. Botanicheskii Zhurnal SSSR 47: 1582–1595. Aleem, A.A. (1974). Marine fungi from Romania. Cercetari Marine, Institutul Roman de Cercetari Marine, Constanta 7: 27–55. Aleem, A.A. (1975). Marine fungi from Rumania. Rapport Commission International pour l’exploration scientifique de la Mer Mediterranee 23: 73–74. Aleem, A.A. (1978). New records of marine fungi from the Red Sea. Bull. Fac. Sci., King Abdel-Aziz University. Jeddah 2: 131–132. 257 Aleem, A.A. (1980a). Pythium marinum Sparrow (Phycomycetes) infesting Porphyra leucosticta Thuret in the Mediterranean Sea. Bot. Mar. 23: 405–407. Aleem, A.A. (1980b). Distribution and ecology of marine fungi in Sierra Leone (tropical West Africa). Bot. Mar. 23: 679–688. Aleem, A.A. and Malibari, A.A. (1981). Studies in tropical marine fungi I. Mangrove fungi from Sierra Leone (West Africa). 1. Deuteromycetes. Bull. Fac. Sci., King Abdul Aziz Univ. Jeddah 5: 51–58. Al-Hebshi, M.O. (2015). Diversity of marine fungi of Arabian Gulf, Saudi Arabia: studies at morphological and molecular levels, M.Sc. Thesis. Saudi Arabia, King Saud University. Alias, S.A. and Jones, E.B.G. (2000a). Colonization of mangrove wood by marine fungi at Kuala Selangor mangrove stand, Malaysia. In: Hyde, K.D., Ho, W.H., and Pointing, S.B. (Eds.), Aquatic mycology across the millennium. Fungal Diversity Press, Hong Kong, 9–21. Alias, S.A. and Jones, E.B.G. (2000b). Vertical distribution of marine fungi on Rhizophora apiculata at Morib mangrove, Selangor, Malaysia. Mycoscience 41: 431–436. Alias, S.A. and Jones, E.B.G. (2009). Marine fungi from mangroves of Malaysia. Institute of Ocean and Earth studies (IOES). No. 8. University of Malaya, Kuala Lumpur. Alias, S.A. and Jones, E.B.G. (2010). Fungi from mangroves of Malaysia. Institute of Ocean and Earth Science. Universiti Malaya, Kuala Lumpur. Alias, S.A., Kuthubutheen, A.J., and Jones, E.B.G. (1994). Fasciatispora lignicola sp. nov. Amphisphaeriaceae, Ascomycotina) from drift mangrove wood. Mycotaxon 52: 77–82. Alias, S.A., Hyde, K.D., and Jones, E.B.G. (1996). Pyrenographa xylographoides from Malaysian and Australian mangroves. Mycol. Res. 100: 580–582. Alias, S.A., Jones, E.B.G., and Torres, J. (1999). Intertidal fungi from the Philippines, with a description of Acrocordiopsis sphaerica sp. nov. (Ascomycota). Fungal Divers. 2: 35–41. Alias, S.A., Kuthubutheen, A.J., and Jones, E.B.G. (1995). Frequency of occurrence of fungi on wood in Malaysian mangroves. Hydrobiologia 295: 97–106. Alias, S.A., Moss, S.T., and Jones, E.B.G. (2001). Cucullosporella mangrovei, ultrastructure of ascospores and their appendages. Mycoscience 42: 405–411. Alias, S.A., Zainuddin, N., and Jones, E.B.G. (2010). Biodiversity of marine fungi in Malaysian mangroves. Bot. Mar. 53: 545–554. Amend, A., Burgaud, G., Cunliffe, M., Edgcomb, V.P., Ettinger, C.L., Gutiérrez, M.H., Heitman, J., Hom, E.F.Y., Ianiri, G., Jones, A.C., et al. (2019). Fungi in the marine environment: open questions and unsolved problems. mBio 10: e01189–18. Am-In, S., Yongmanitchai, W., and Limtong, S. (2008). Kluyveromyces siamensis sp. nov., an ascomycetous yeast isolated from water in a mangrove forest in Ranong province, Thailand. FEMS Yeast Res. 8: 823–828. Ananda, K. and Sridhar, K.R. (2002). Diversity of endophytic fungi in the roots of mangrove species on the West Coast. Can. J. Micorbiol. 48: 871–878. Ariyawansa, H.A., Hyde, K.D., Jayasiri, S.C., Buyck, B., Chethana, K.W.T., Dai, D.Q., Dai, Y.C., Daranagama, D.A., Jayawardena, R.S., Lücking, R., et al. (2015). Fungal diversity notes 111–252—taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers. 75: 27–274. Azevedo, E., Rebelo, R., Caeiro, M.F., and Barata, M. (2010). Diversity and richness of marine fungi on two Portuguese marinas. Nova Hedwigia 90: 521–531. Azevedo, E., Rebelo, R., Caeiro, M.F., and Barata, M. (2011). Biodiversity and characterization of marine mycota from Portuguese waters. Animal Biodivers. Conserv. 34: 205–215. 258 K.-L. Pang et al.: Country reports of marine mycological research Azevedo, E., Rebelo, R., Caeiro, M.F., and Barata, M. (2012). Use of drift substrates to characterize marine fungal communities from the west coast of Portugal. Mycologia 104: 623–632. Azevedo, E., Barata, M., Marques, M.I., and Caeiro, M.F. (2017). Lulworthia atlantica: a new species supported by molecular phylogeny and morphological analysis. Mycologia 109: 287–295. Azevedo, E., Barata, M., and Caeiro, M.F. (2018). Morphological and phylogenetic analyses of Nia vibrissa, a marine Basidiomycota collected in Portuguese waters. Reg. Stud. Mar. Sci. 23: 53–59. Bakhit, M.S. and Abdel-Wahab, M.A. (2022). Safagamyces marinus gen. et sp. nov. (Halosphaeriaceae, Sordariomycetes) from Red Sea mangroves, Egypt. Phytotaxa 568: 221–229. Banos, S., Gysi, D.M., Richter-Heitmann, T., Glockner, F.O., Boersma, M., Wiltshire, K.H., Gerdts, G., Wichels, A., and Reich, M. (2020). Seasonal dynamics of pelagic mycoplanktonic communities: interplay of taxon abundance, temporal ioccurrence, and biotic interactions. Front. Microbiol. 11: 1305. Barata, M. (2002). Fungi on the halophytes Spartina maritima in salt marshes. In: Hyde, K.D. (Ed.), Fungi in marine environments. Fungal Diversity Research Series, Hong Kong, pp. 179–193. Barata, M. (2006). Marine fungi from Mira River in salt marsh in Portugal. Rev. Iberoam. Micol. 23: 179–184. Barata, M., Basilio, M.C., and Baptista-Ferreira, J.L. (1997). Nia globospora, a new marine gastromycete on baits of Spartina maritima in Portugal. Mycol. Res. 101: 687–690. Barghoorn, E.S. and Linder, D.H. (1944). Marine fungi: their taxonomy and biology. Farlowia 1: 395–467. Bärlocher, F. and Moulton, V.D. (1999). Spartina alterniflora in two New Brunswick salt marshes. I. Growth and decomposition. Bull. Mar. Sci. 64: 299–305. Bärlocher, F., Newell, S.Y., and Arsuffi, T.L. (1989). Digestion of Spartina alterniflora Loisel material with and without fungal constituents by the periwinkle Littorina irrorata Say (Mollusca: Gastropoda). J. Exp. Mar. Biol. Ecol. 130: 45–53. Becker, G. and Kohlmeyer, J. (1958). Deterioration of wood by marine fungi in India and its special significance for fishing crafts. J. Timber Dryer’s Preserv. Assoc. India 4: 1–10. Berry, O., Briand, E., Bagot, A., Chaigné, M., Meslet-Cladière, L., Wang, J., Grovel, O., Jansen, J.J., Ruiz, N., du Pont, T.R., et al. (2023). Deciphering interactions between the marine dinoflagellate Prorocentrum lima and the fungus Aspergillus pseudoglaucus. Environ. Microbiol. 25: 250–267. Bertrand, S., Guitton, Y., and Roullier, C. (2017). Successes and pitfalls in automated dereplication strategy using liquid chromatography coupled to mass spectrometry data: a CASMI 2016 experience. Phytochem. Lett. 21: 297–305. Besitulo, A., Moslem, M.A., and Hyde, K.D. (2010). Occurrence and distribution of fungi in a mangrove forest on Siargao Island, Philippines. Bot. Mar. 53: 535–543. Bokhary, H.A., Moslem, M.A., and Parvez, S. (1992). Marine fungi of the Arabian Gulf coast and Saudi Arabia. Microbiologica 15: 281–290. Boland, G.J. and Grund, D.W. (1979). Fungi from the salt marshes of Minas Basin, Nova Scotia. Proc. Nova Scotian Inst. Sci. 29: 393–404. Borse, B.D. (1984). Marine fungi from India – I. Indian Bot. Rep. 3: 156–157. Borse, B.D. (1985). Marine fungi from India – II. Curr. Sci. 17: 881–882. Borse, B.D. (1987). New species of Aigialus from India. Trans. Br. Mycol. Soc. 88: 424–426. Borse, B.D. and Hyde, K.D. (1989). Marine fungi from India. III. Acrocordiopsis patilii gen. et sp. nov. from mangrove wood. Mycotaxon 34: 535–540. Borse, B.D., Borse, K.N., Pawar, N.S., and Tuwar, A.R. (2013). Marine fungi from India –XII: a revised check list. Indian J. Geol. Mar. Sci. 42: 110–119. Bovio, E., Gnavi, G., Prigione, V., Spina, F., Denaro, R., Yakimov, M., Calogero, R., Crisafi, F., and Varese, G.C. (2017). The culturable mycobiota of a Mediterranean marine site after an oil spill: isolation, identification and potential application in bioremediation. Sci. Total Environ. 576: 310–318. Bovio, E., Fauchon, M., Toueix, Y., Mehiri, M., Varese, G.C., and Hellio, C. (2019a). The sponge-associated fungus Eurotium chevalieri MUT 2316 and its bioactive molecules: potential applications in the field of antifouling. Mar. Biotech. 21: 743–752. Bovio, E., Garzoli, L., Poli, A., Luganini, A., Villa, P., Musumeci, R., McCormack, G.P., Cocuzza, C.E., Gribaudo, G., Mehiri, M., et al. (2019b). Marine fungi from the sponge Grantia compressa: biodiversity, chemodiversity, and biotechnological potential. Mar. Drugs 17: 220. Bruni, V., Grasso, S., and La Ferla, R. (1982). Sulla presneza di funghi lignicoli in aqua costiere della Sicilia nord-orietale. Mem. Biol. Mar. Ocean. 12: 27–37. Burgaud, G., Le Calvez, T., Arzur, D., Vandenkoornhuyse, P., and Barbier, G. (2009). Diversity of culturable marine filamentous fungi from deepsea hydrothermal vents. Environ. Microbiol. 11: 1588–1600. Burgaud, G., Arzur, D., Durand, L., Cambon-Bonavita, M.A., and Barbier, G. (2010). Marine culturable yeasts in deep-sea hydrothermal vents: species richness and association with fauna. FEMS Microbiol. Ecol. 73: 121–133. Burgaud, G., Arzur, D., Sampaio, J.P., and Barbier, G. (2011). Candida oceani sp. nov., a novel yeast isolated from a Mid-Atlantic Ridge hydrothermal vent (–2300 meters). Anton Leeuw. Int. J. G. 100: 75–82. Burgaud, G., Edgcomb, V.P., Hassett, B.T., Li, W., Mara, P., Philippe, A., Phule, P., Prado, S., Quémener, M., and Roullier, C. (2022). Marine fungi. In: Stal, L.J., and Cretoiu, M.S. (Eds.), The marine microbiome. Cham: Springer, pp. 243–295. Calabon, M.S., Jones, E.B.G., Promputtha, I., and Hyde, K.D. (2021). Fungal biodiversity in salt marsh ecosystems. J. Fungi 7: 1–72. Calado, M.L., Carvalho, L., Pang, K.L., and Barata, M. (2015). Diversity and Ecological characterization of sporulating higher marine fungi associated with Spartina maritima (Curtis) Fernald in two Portuguese salt marshes. Microb. Ecol. 70: 612–633. Calado, M.L., Carvalho, L., Barata, M., and Pang, K.L. (2019). Potential roles of marine fungi in the decomposition process of standing stems and leaves of Spartina maritima. Mycologia 111: 371–383. Calado, M.D.L., Silva, J., Alves, C., Susano, P., Santos, D., Alves, J., Martins, A., Gaspar, H., Pedrosa, R., and Campos, M.J. (2021). Marine endophytic fungi associated with Halopteris scoparia (Linnaeus) Sauvageau as producers of bioactive secondary metabolites with potential dermocosmetic application. PLoS One 16: e0250954. Campbell, J. (2005). Neotypification of Lulworthia fucicola. Mycologia 97: 549–551. Campbell, J., Anderson, J.L., and Shearer, C.A. (2003). Systematics of Halosarpheia based on morphological and molecular data. Mycologia 95: 530–552. Campbell, J., Volkmann-Kohlmeyer, B., Gräfenhan, T., Spatafora, J.W., and Kohlmeyer, J. (2005). A re-evaluation of Lulworthiales: relationships based on 18S and 28S rDNA. Mycol. Res. 109: 556–568. Campbell, J., Inderbitzin, P., Kohlmeyer, J., and Volkmann-Kohlmeyer, B. (2009). Koralionastetales, a new order of marine Ascomycota in the Sordariomycetes. Mycol. Res. 113: 373–380. Chen, S.F. (2020). An obligately halophytic chytrid. In: Paper presented at the 2020 Annual Joint Meeting of Mycological Society ROC and Taiwan K.-L. Pang et al.: Country reports of marine mycological research Society of Microbial Ecology & Fungal Ecology Conference, Taipei, Taiwan. Chinworungsee, M., Kittakoop, P., Isaka, M., Rungrod, A., Tantichaeron, M., and Thebaranonth, Y. (2001). Antimalarial Haloroselinic acid from the marine fungus Halorosellinia oceanica. Bioorg. Med. Chem. Lett. 11: 1965–1969. Ciobanu, M.C., Burgaud, G., Dufresne, A., Breuker, A., Redou, V., Maamar, S.B., Gaboyer, F., Vandenabeele-Trambouze, O., Lipp, J.S., Schippers, A., et al. (2014). Microorganisms persist at record depths in the subseafloor of the Canterbury Basin. ISME J. 8: 1370–1380. Cochereau, B., Meslet-Cladière, L., Pouchus, Y.F., Grovel, O., and Roullier, C. (2022). Halogenation in fungi: what do we know and what remains to be discovered? Molecules 27: 3157. Comeau, A.M., Vincent, W.F., Bernier, L., and Lovejoy, C. (2016). Novel chytrid lineages dominate fungal sequences in diverse marine and freshwater habitats. Sci. Rep. 6: 30120. Cooper, C., Walker, A.K., Sheng, X., Simons, M., Ronda, L., Mozzarelli, A., and Reeder, B.J. (2022). Endophytic fungi from marine macroalgae in Nova Scotia. Northeast. Nat. 29: 295–310. Cotton, A.D. (1909). Notes on marine pyrenomycetes. Trans. Br. Mycol. Soc. 3: 92–99. Cribb, A.B. and Cribb, J.W. (1955). Marine fungi from Queensland. 1. Papers of the Department of Botany University of Queensland 3: 77–81. Cribb, A.B. and Cribb, J.W. (1956). Marine fungi from Queensland. 2. Papers of the Department of Botany University of Queensland 3: 97–105. Cribb, A.B. and Cribb, J.W. (1960). Marine fungi from Queensland. 3. Papers of the Department of Botany University of Queensland 4: 40–44. Cribb, A.B. and Cribb, J.W. (1969). Some marine fungi from the great Barrier reef area. Queensl. Nat. 19: 118–120. Cribb, A.B. and Herbert, J.W. (1954). Three species of fungi parasitic on marine algae in Tasmania. Papers of the Department of Botany University of Queensland 3: 9–13. Crouan, P.L. and Crouan, H.M. (1867). Florule du Finistère. Klincksieck. F, Paris. Cunliffe, M. (2023). Who are the marine fungi? Environ. Microbiol. 25: 131–134. Cuomo, V., Vanzanella, F., and Cinelli, F. (1983). I funghi alhicoli marini del Isola d’Ischia. In: Frache, R. and Strobel, F. (Eds.), 4 Congresso Assoclazione Italiana di Oceanologgia e Limnologia, pp. 1–9. Cuomo, V., Vanzanella, F., Fresi, E., Cinelli, F., and Mazzella, L. (1985). Fungal flora of Posidonia oceanica and its ecological significance. Trans. Br. Mycol. Soc. 84: 35–40. Cuomo, V., Jones, E.B.G., and Grasso, S. (1988). Occurrence and distribution of marine fungi along the coast of the Mediterranean Sea. Prog. Oceanogr. 21: 189–200. Damare, V. and Raghukumar, S. (2006). Morphology and physiology of the marine straminipilan fungi, the aplanochytrids isolated from the equatorial Indian Ocean. Indian J. Mar. Sci. 35: 326–340. Damare, S., Raghukumar, C., and Raghukumar, S. (2006). Fungi in deep–sea sediments of the Central Indian Basin. Deep-Sea Res. 53: 14–27. Dayarathne, M.C., Abeywickrama, P., Jones, E.B.G., Bhat, D.J., Chomnunti, P., and Hyde, K.D. (2017). Multi-gene phylogeny of Jattaea bruguierae, a novel asexual morph from Bruguiera cylindrica. Stud. Fungi 2: 235–245. Dayarathne, M., Jones, E.B.G., Maharachchikumbura, S., Devadatha, B., Khongphinitbunjong, K., Chomnunti, P., and Hyde, K.D. (2020a). Morpho-molecular characterization of microfungi associated with marine based habitats. Mycosphere 11: 1–188. Dayarathne, M.C., Wanasinghe, D.N., Devadatha, B., Abeywickrama, P., Jones, E.B.G., Chomnunti, P., Sarma, V.V., Hyde, K.D., Lumyong, S., and 259 McKenzie, E.H.C. (2020b). Modern taxonomic approaches to identifying diatrypaceous fungi from marine habitats, with a novel genus Halocryptovalsa Dayarathne et K.D. Hyde, gen. nov. Cryptogam. Mycol. 41: 21–67. d’Entremont, T.W., Migicovsky, Z., López‐Gutiérrez, J.C., and Walker, A.K. (2021). Saltmarsh rhizosphere fungal communities vary by sediment type and dominant plant species cover in Nova Scotia, Canada. Environ. Microbiol. Rep. 13: 458–463. Desmaziéres, J.B.H.J. (1849). Plantes cryptogames de France, 2nd ed. No. 1778. NA: Lille. Devadatha, B., Sarma, V.V., Wanasinghe, D.N., Hyde, K.D., and Jones, E.B.G. (2017). Introducing the new Indian mangrove species, Vaginatispora microarmatispora (Lophiostomataceae) based on morphology and multigene phylogenetic analysis. Phytotaxa 329: 139–149. Devadatha, B., Sarma, V.V., Ariyawansa, A., and Jones, E.B.G. (2018). Deniquelata vittalii sp. nov., a novel Indian saprobic marine fungus on Suaeda monoica and two new records of marine fungi from Muthupet mangroves, East coast of India. Mycosphere 9: 565–582. Devadatha, B., Mehta, N., Wanasinghe, D.N., Baghela, A., and Sarma, V.V. (2019). Vittaliana mangrovei, gen. nov., sp. nov. Phaeosphaeriaceae. from mangroves near Pondicherry India., based on morphology and multigene phylogeny. Cryptogam. Mycol. 40: 117–132. Devadatha, B., Jones, E.B.G., Ghate, S.D., and Sarma, V.V. (2021a). Biodiversity of marine fungi in mangroves with reference to Muthupet mangroves, Tamil Nadu, east coast of India. Mar. Biodivers. 51: 88. Devadatha, B., Jones, E.B.G., Pang, K.L., Abdel-Wahab, M.A., Hyde, K.D., Sakayaroj, J., Bahkali, A.H., Calabon, M.S., Sarma, V.V., Sutreong, S., et al. (2021b). Occurrence and geographical distribution of mangrove fungi. Fungal Divers. 106: 137–227. Dezaire, A., Marchand, C.H., Vallet, M., Ferrand, N., Chaouch, S., Mouray, E., Larsen, A.K., Sabbah, M., Lemaire, S.D., Prado, S., et al. (2020). Secondary metabolites from the culture of the marine-derived fungus Paradendryphiella salina PC 362H and evaluation of the anticancer activity of its metabolite hyalodendrin. Mar. Drugs 18: 191. Diao, L.G., Jin, J., and Luo, L. (2009). Wood-inhabiting marine fungi from the coast of Shandong, China Ⅶ. Mycosystema 28: 483–489. Dias, A.C.D.S., Ruiz, N., Couzinet-Mossion, A., Bertrand, S., Duflos, M., Pouchus, Y.-F., Barnathan, G., Nazih, H., and Wielgosz-Collin, G. (2015). The marine-derived fungus Clonostachys rosea, source of a rare conjugated 4-Me-6E,8E-hexadecadienoic acid reducing viability of MCF-7 breast cancer cells and gene expression of lipogenic enzymes. Mar. Drugs 13: 4934–4948. Doguet, G. (1962). Mycologie, Digitatispora marina, ng, n. sp. nov., basidiomycete marin. Comptes rendus hebdomadaires des séances de l’Academie des Sciences 254: 4336. Du, J.J. and Jin, J. (2010). Wood inhabiting marine fungi from the coast of Shandong, China Ⅷ. Mycosystema 29: 463–466. Dupont, J., Magnin, S., Rousseau, F., Zbinden, M., Frebourg, G., Samadi, S., Richer de Forges, B., and Jones, E.B.G. (2009). Molecular and ultrastructural characterization of two ascomycetes found on sunken wood off Vanuatu Islands in the deep Pacific Ocean. Mycol. Res. 113: 1351–1364. Ekanayake, K.B., Gnanapragasam, J.J., Ranawana, K., Vidanapathirana, D.R., Abeyawardhana, U.T., Fernando, C., McQueen, A., Weston, M.A., and Symonds, M.R.E. (2022). Ecological and environmental predictors of escape among birds on a large tropical island. Behav. Ecol. Sociobiol. 76: 31. Elsebai, M.F., Ghabbour, H.A., Legrave, N., Fontaine-Vive, F., and Mehiri, M. (2018). New bioactive chlorinated cyclopentene derivatives from the marine-derived fungus Phoma sp. Med. Chem. Res. 27: 1885–1892. 260 K.-L. Pang et al.: Country reports of marine mycological research El-Sharouny, H.M., Raheem, A.M., and Abdel-Wahab, M.A. (1998). Manglicolous fungi of the Red Sea in upper Egypt. Microbiol. Res. 153: 81–96. El-Sharouny, H.M., Abd-Elaah, G.A., and Abdel-Wahab, M.A. (1999). Fungal species isolated from algae and decayed leaves and the combined effect on salinity and temperature on three marine fungi. In: Abdel-Razak, A. (Ed.), Proceedings of the 2nd international conference on fungi: hopes and challenges. Cairo: Azhar University Press, pp. 39–52. El-Sharouny, H.M., Gherbawy, Y.A.M.H., and Abdel-Aziz, F.A. (2009). Fungal diversity in brackish and saline lakes in Egypt. Nova Hedwigia 89: 437–450. Eriksson, O. (1964). Nectriella laminariae n. sp. in stipes of a Laminaria. Sven. Bot. Tidskr. 58: 233–236. Eriksson, O. (1973). Orbilia marina, an over-looked discomycete on members of Fucales. Sven. Bot. Tidskr. 67: 208–210. Eriksson, O.E. (1981). The families of bitunicate ascomycetes. Opera. Bot. 60: 1–220. Eriksson, O. (1982). Notes on ascomycetes and coelomycetes from NW Europe. Mycotaxon 15: 189–202. Eriksson, O. (1992). The non-lichenized pyrenomycetes of Sweden. Lund: SBT-förlaget. Eriksson, O. (2014). Checklist of the non-lichenized ascomycetes of Sweden. Symb. Bot. Ups. 36: 1–499. Erneholm, N. (1972). Marina svampar: studier i den tempererade och tropiska marina svampfloran, Ph.D. Thesis. Goteborg, University of Goteborg. Ettinger, C.L. and Eisen, J.A. (2020). Fungi, bacteria and oomycota opportunistically isolated from the seagrass, Zostera marina. PLoS One 15: e0236135. Ettinger, C.L., Vann, L.E., and Eisen, J.A. (2021). Global diversity and biogeography of the Zostera marina mycobiome. Appl. Environ. Microbiol. 87: e0279520. Feldmann, G. (1957). Un nouvel Ascomycete parasite d’une algue marine: Chadefaudia marina. Rev. Gen. Bot. 64: 140–152. Fell, J.W., Ahearn, D.G., Meyers, S.P., and Roth, F.J., Jr. (1960). Isolation of yeasts from Biscayne Bay, Florida and adjacent benthic areas. Limnol. Oceanogr. 5: 366–371. Fernand, M.G., Roullier, C., Guitton, Y., Lalande, J., Lacoste, S., Dupont, J., Ruiz, N., Pouchus, Y.F., Rahariniaina, C., and Ranaivoson, E. (2017). Fungi isolated from Madagascar shrimps-investigation of the Aspergillus niger metabolism by combined LC-MS and NMR metabolomics studies. Aquaculture 479: 750–758. Figueira, D. and Barata, M. (2007). Marine fungi from two sandy beaches in Portugal. Mycologia 99: 20–23. Flewelling, A.J., Ellsworth, K.T., Sanford, J., Forward, E., Johnson, J.A., and Gray, C.A. (2013). Macroalgal endophytes from the Atlantic Coast of Canada: a potential source of antibiotic natural products? Microorganisms 1: 175–187. Fries, E. (1822). Systema mycologicum 2(1). Lund. Fries, N. (1965). Vitamins and other organic growth factors. In: Ainsworth, G.C. and Sussman, A.S. (Eds.), The fungi. Vol. I. The fungal cell. Academic Press, New York, pp. 491–523. Fries, N. (1979). Physiological characteristics of Mycosphaerella ascophylli, a fungal endophyte of the marine brown alga Ascophyllum nodosum. Physiol. Plant. 45: 117–121. Fries, N. and Thorén-Tolling, K. (1978). Identity of the fungal endophyte of Ascophyllum with Mycosphaerella ascophylli established by means of fluorescent antibody techniques. Bot. Mar. 21: 409–411. Fryar, S.C., Haelewaters, D., and Catcheside, D.E.A. (2019). Annabella australiensis gen. et sp. nov. (Helotiales, Cordieritidaceae) from South Australian mangroves. Mycol. Progr. 18: 973–981. Fryar, S.C., Hyde, K.D., and Catcheside, D.E.A. (2020). A survey of marine fungi on wood in South Australia. Bot. Mar. 63: 469–478. Furtado, S.E.J. and Jones, E.B.G. (1980). The colonization selected naturally durable timbers by marine fungi and borers. Bull. Liaison C.O.I.P.M. 8: 63–93. Gacutan, M.V.C. and Uyenco, F.R. (1983). Marine fungi from batan, Aklan. Nat. Sci. Appl. Bull. 35: 1–16. Gaertner, A. (1980). Quantitative studies on the marine phycomycetes, chytrids and higher mycelial fungi of the upper Tay estuary. Proc. R. Soc. Edinb. B 78: 57–78. Gaertner, A. (1982). Lower marine fungi from the Northwest African upwelling areas and from the Atlantic off Portugal. Meteor. Forschergeb. Ergebn. 34: 9–30. Galagan, J.E., Calvo, S.E., Cuomo, C., Ma, L.J., Wortman, J.R., Batzoglou, S., Lee, S.I., Baştürkmen, M., Spevak, C.C., Clutterbuck, J., et al. (2005). Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature 438: 1105–1115. Garzoli, L., Gnavi, G., Varese, G.C., and Picco, A.M. (2014). Mycobiota associated with the rhodophyte alien species Asparagopsis taxiformis (Delile) trevisan de Saint-Leon in the Mediterranean Sea. Mar. Ecol. 36: 959–968. Garzoli, L., Tamma, F., Tosia, S., Varese, G.C., and Picco, A.M. (2015). Sink or swim: updated knowledge on marine fungi associated with wood substrates in the Mediterranean Sea and hints about their potential to remediate hydrocarbons. Prog. Oceanogr. 137: 140–148. Garzoli, L., Poli, A., Prigione, V., Gnavi, G., and Varese, G.C. (2018). Peacock’s tail with a fungal cocktail: first assessment of the mycobiota associated with the brown alga Padina pavonica. Fungal Ecol. 35: 87–97. Gessner, R.V. (1976). In vitro growth and nutrition of Buergenerula spartinae, a fungus associated with Spartina alterniflora. Mycologia 68: 583–599. Gessner, R.V. (1977). Seasonal occurrence and distribution of fungi associated with Spartina alterniflora from a Rhode Island estuary. Mycologia 69: 477–491. Gessner, R.V. and Goos, R.D. (1973). Fungi from decomposing Spartina alterniflora. Can. J. Bot. 51: 51–55. Gessner, R.V. and Kohlmeyer, J. (1976). Geographical distribution and taxonomy of fungi from salt marsh Spartina. Can. J. Bot. 54: 2023–2037. Ghate, S.D. and Sridhar, K.R. (2015). Contribution to the knowledge of macrofungi in mangroves of the South-West India. Plant Biosyst. 150: 977–986. Gladfelter, A.S., James, T.Y., and Amend, A.S. (2019). Marine fungi. Curr. Biol. 29: R191–R195. Gnavi, G., Ercole, E., Panno, L., Vizzini, A., and Varese, G.C. (2014). Dothideomycetes and Leotiomycetes sterile mycelia isolated from the Italian seagrass Posidonia oceanica based on rDNA data. SpringerPlus 3: 508. Gnavi, G., Garzoli, L., Poli, A., Prigione, V., Burgaud, G., and Varese, G.C. (2017). The culturable mycobiota of Flabellia petiolata: first survey of marine fungi associated to a Mediterranean green alga. PLoS One 12: e0175941. Gonçalves, M.F.M., Vicente, T.F.L., Esteves, A.C., and Alves, A. (2019). Neptunomyces aureus gen. et sp. nov. (Didymosphaeriaceae, K.-L. Pang et al.: Country reports of marine mycological research Pleosporales) isolated from algae in Ria de Aveiro, Portugal. MycoKeys 60: 31–44. Gonçalves, M.F.M., Vicente, T.F.L., Esteves, A.C., and Alves, A. (2020). Novel halotolerant species of Emericellopsis and Parasarocladium associated with macroalgae in an estuarine environment. Mycologia 112: 154–171. Gonçalves, M.F.M., Abreu, A., Hilário, S., and Alves, A. (2021a). Diversity of marine fungi associated with wood baits in the estuary Ria de Aveiro with descriptions of Paralulworthia halima comb. nov., Remispora submersa sp. nov. and Zalerion pseudomaritima sp. nov. Mycologia 113: 664–683. Gonçalves, M.F.M., Paço, A., Escada, L.F., Albuquerque, M.S.F., Pinho, C.A., Saraiva, J., Duarte, A.S., Rocha-Santos, T.A.P., Esteves, A.C., and Alves, A. (2021b). Unveiling biological activities of marine fungi: the effect of sea salt. Appl. Sci. 11: 6008. Gonçalves, M.F.M., Hilário, S., van de Peer, Y., Esteves, A.C., and Alves, A. (2022). Genomic and metabolomic analyses of the marine fungus Emericellopsis cladophorae: insights into saltwater adaptability mechanisms and its biosynthetic potential. J. Fungi 8: 31. González, M.C., Hanlin, R.T., and Ulloa, M. (2001). A checklist of higher marine fungi of Mexico. Mycotaxon 80: 241–253. Grasso, S., La Ferla, R., and Jones, E.B.G. (1985). Lignicolous marine fungi in a harbour environment (Milazzo). Bot. Mar. 28: 259–264. Grasso, S., Panebianco, C., and La Ferla, R. (1990). Lignicolous marine fungi in the straits of Messina, Italy. Hydrobiologia 206: 149–154. Grossart, H.P., van den Wyngaert, S., Kagami, M., Wurzbacher, C., Cunliffe, M., and Rojas-Jimenz, K. (2019). Fungi in aquatic ecosystems. Nat. Rev. Microbiol. 17: 339–354. Grovel, O., Pouchus, Y.F., and Verbist, J.F. (2003). Accumulation of gliotoxin, a cytotoxic mycotoxin from Aspergillus fumigatus, in blue mussel (Mytilus edulis). Toxicon 42: 297–300. Grunwald, A.L., Berrué, F., Overy, D.P., and Kerr, R.G. (2016). Isolation of iqalisetins A and B from a tolypocladium sp. isolated from marine sediment from Frobisher Bay in Canada’s arctic. Can. J. Chem. 94: 444–448. Grunwald, A.L., Berrue, F., Robertson, A.W., Overy, D.P., and Kerr, R.G. (2017). Mortiamides A–D, cyclic heptapeptides from a novel Mortierella sp. obtained from Frobisher Bay. J. Nat. Prod. 80: 2677–2683. Guerriero, A., D’Ambrosio, M., Cuomo, V., Vanzanella, F., and Pietra, F. (1988). Dendryphiellin A, the first fungal trinor-eremophilane. Isolation from the marine Deuteromycete Dendryphiella salina (Sutherland) Pugh et Nicot. Helv. Chim. Acta 71: 57–61. Guerriero, A., D’Ambrosio, M., Cuomo, V., Vanzanella, F., and Pietra, F. (1989). Novel trinor-ermophilanes (Dendryphiellin C, C, and D), ermophilanes (Dendryphiellin E, F, and G) and branched C9-carboxylic acids (Dendryphiellions Acid A and B) from the marine Deuteromycete Dendryphiella salina (Sutherland) Pugh et Nicot. Helv. Chim. Acta 72: 418–446. Gustafsson, U. and Fries, N. (1956). Nutritional requirements of some marine fungi. Physiol. Plant. 9: 462–465. Han, P.J., Sun, J.Q., and Wang, L. (2022). Two new sexual Talaromyces species discovered in estuary soil in China. J. Fungi 8: 36. Hagestad, O.C., Hou, L., Andersen, J.H., Hansen, E.H., Altermark, B., Li, C., Kuhnert, E., Cox, R.J., Crous, P.W., Spatafora, J.W., et al. (2021). Genomic characterization of three marine fungi, including Emericellopsis atlantica sp. nov. with signatures of a generalist lifestyle and marine biomass degradation. IMA Fungus 12: 1–23. 261 Hassett, B.T., Ducluzeau, A.-L.L., Collins, R.E., and Gradinger, R. (2017). Spatial distribution of aquatic marine fungi across the western Arctic and sub-arctic. Environ. Microbiol. 19: 475–484. Hassett, B.T., Borrego, E.J., Vonnahme, T.R., Rämä, T., Kolomiets, M.V., and Gradinger, R. (2019). Arctic marine fungi: biomass, functional genes, and putative ecological roles. ISME J. 13: 1484–1496. Hattori, T., Sakayaroj, J., Jones, E.B.G., Suetrong, S., Preedanon, S., and Klaysuban, A. (2014). Three species of Fulvifomes (Basidiomycota, Hymenochaetales) associated with rots on mangrove tree Xylocarpus granatum in Thailand. Mycoscience 55: 344–354. Henningsson, M. (1974). Aquatic lignicolous fungi in the Baltic and along the west coast of Sweden. Sven. Bot. Tidskr. 68: 401–425. Henningsson, M. (1976a). Degradation of wood by some fungi from the Baltic and the west coast of Sweden. Mater. Org. 3: 509–519. Henningsson, M. (1976b). Studies on aquatic lignicolous fungi from Swedish coastal waters, Ph.D. thesis. Uppsala, Acta Universitatis Upsaliensis. Ho, H.H. and Jong, S.C. (1990). Halophytophthora gen. nov., a new member of the family Pythiaceae. Mycotaxon 36: 377–382. Ho, H.H., Chang, H.S., and Hsieh, S.Y. (1991). Halophytophthora kandeliae, a new marine fungus from Taiwan. Mycologia 83: 419–424. Ho, H.H., Chang, H.S., and Huang, S.H. (2003). Halophytophthora elongata, a new marine species from Taiwan. Mycotaxon 85: 417–422. Hoang, T.P.T., Roullier, C., Boumard, M.C., Robiou du Pont, T., Nazih, H., Gallard, J.F., Benidir, M.A., and Grovel, O. (2018). Metabolomics-driven discovery of meroterpenoids from a mussel-derived Penicillium ubiquetum. J. Nat. Prod. 81: 2501–2511. Hodhod, M.S., Abdel-Wahab, M.A., Bahkali, A.H., and Hyde, K.D. (2012). Amarenographium solium sp. nov. From Yanbu mangroves in the Kingdom of Saudi Arabia. Cryptogam. Mycol. 33: 285–294. Höhnk, W. (1955). Studie zur Brack- und Seewassermykologie. Höhere Pilze des submersen Holzes 3: 199–227. Holt, C.C., Boscaro, V., Van Steenkiste, N.W.L., Herranz, M., Mathur, V., Irwin, N.A.T., Buckholtz, G., Leander, B.S., and Keeling, P.J. (2022). Microscopic marine invertebrates are reservoirs for cryptic and diverse protists and fungi. Microbiome 10: 161. Hsieh, S.Y. (2002). Nine arenicolous marine ascomycetes from Taiwan. Fungal Sci. 17: 39–47. Hsieh, S.Y., Yuan, G.F., and Chang, H.S. (2002). Higher marine fungi from Taiwan. Food Industry Research & Development Institute, Hsinchu, Taiwan (ROC). Hsieh, S.Y., Moss, S.T., and Jones, E.B.G. (2007). Ascoma development in the marine ascomycete Corollospora gracilis (Halosphaeriales, Hypocreomycetidae, Sordariomycetes). Bot. Mar. 50: 1–12. Huang, H.R., Feng, X.L., She, Z.G., Lin, Y.C., Vrijmoed, L.L.P., and Jones, E.B.G. (2005). 1-(2, 6-Dihydroxyphenyl) butanone. Acta Cryst. E61: 0282–0283. Hughes, G.C. (1974). Geographical distribution of the higher marine fungi. Veroffentlichungen Inst. Meeresforsch. Bremerhaven 5: 419–441. Hughes, G.C. (1975). Studies of fungi in oceans and estuaries since 1961. Lignicolous, caulicolous and folicolous species. Oceanogr. Mar. Biol. Annu. Rev. 13: 69–180. Hyde, K.D. (1989). Caryospora mangrovei sp. nov. and notes on marine fungi from Thailand. Trans. Mycol. Soc., Jpn. 30: 333–341. Hyde, K.D. (1990). Intertidal fungi from warm temperate mangroves of Australia, including Tunicatispora australiensis gen. et sp. nov. Aust. Syst. Bot. 3: 711–718. 262 K.-L. Pang et al.: Country reports of marine mycological research Hyde, K.D. (1992a). Intertidal mangrove fungi from the west coast of Mexico, including one new genus and two new species. Mycol. Res. 96: 25–30. Hyde, K.D. (1992b). Julella avicenniae (Borse) comb. nov. (Thelennellaceae) from intertidal mangrove wood and miscellaneous fungi from the North East Coast of Queensland. Mycol. Res. 96: 939–942. Hyde, K.D. (1992c). The genus Saccardoella from intertidal mangrove wood. Mycologia 84: 803–810. Hyde, K.D. (1993a). Cryptovalsa halosarceicola sp. nov. an intertidal saprotroph of Halosarceia halocnemoides. Mycol. Res. 97: 799–800. Hyde, K.D. (1993b). Fungi from palms. V. Phomatospora nypae sp. nov. and notes on marine fungi from Nypa fruticans in Malaysia. Sydowia 45: 199–203. Hyde, K.D. (1995). Eutypella naqsii sp. nov. from intertidal Avicennia. Mycol. Res. 99: 1462–1464. Hyde, K.D. and Alias, S.A. (2000). Biodiversity and distribution of fungi associated with decomposing Nypa fruticans. Biodivers. Conserv. 9: 393–402. Hyde, K.D. and Borse, B.D. (1986a). Marine fungi from Seychelles–V. Biatriospora marina gen. et sp. nov., from mangrove wood. Mycotaxon 26: 263–270. Hyde, K.D. and Borse, B.D. (1986b). Marine fungi from Seychelles–VI. Massarina velataspora. A new marine ascomycotina from mangrove wood. Mycotaxon 27: 161–167. Hyde, K.D. and Nakagiri, A. (1989). A new species of Oxydothis from the mangrove pam Nypa fruticans. Trans. Mycol. Soc., Jpn. 30: 60–75. Hyde, K.D. and Nakagiri, A. (1991). Mangrovispora pemphii gen. et sp. nov., a new marine fungus from Pemphis acidula. Syst. Ascomycet. 10: 19–25. Hyde, K.D. and Rappaz, F. (1993). Eutypa bathurstensis sp. nov. from intertidal Avicennia. Mycol. Res. 97: 861–864. Hyde, K.D. and Jones, E.B.G. (1992). Intertidal mangrove fungi: Pedumispora gen. nov. (Diaporthales). Mycol. Res. 96: 78–80. Hyde, K.D., Chalermongse, A., and Boonthavikoon, T. (1990). Ecology on intertidal fungi at Ranong mangrove, Thailand. Trans. Mycol. Soc., Jpn. 31: 17–28. Hyde, K.D., Chalermpongse, and A., and Boonthavikoon, T. (1993). The distribution of intertidal fungi on Rhizophora apiculata. In: Morton, B. (Ed.), The marine biology of the South China sea. Proceedings of the first international Conference on the marine Biology of Hong Kong and south China sea, Hong Kong. University of Hong Kong Press, Hong Kong, 643–652. Hyde, K.D., Hongsanan, S., Jeewon, R., Bhat, D.J., Mckenzie, E.H.C., Jones, E.B.G., Phookamsak, R., Ariyawansa, H.A., Boonmee, S., Zhao, Q., et al. (2016). Fungal diversity notes 367–490: taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers. 80: 1–270. Imhoff, J.F. (2016). Natural products from marine fungi-still an underrepresented resource. Mar. Drugs 14: 19. Isaka, M., Suyarnsestakorn, C., Tanticharoen, M., Kongsaeree, P., and Thebtaranonth, Y. (2002). Aigialomycins A-E, new resorcylic macrolides from the marine mangrove fungus Aigialus parvus. J. Org. Chem. 67: 1561–1566. Isaka, M., Chinthanom, P., Kongthong, S., Supothina, S., Ittiworapong, P., and Hamigeromycins, C.-G. (2010). 14-membered macrolides from the fungus Hamigera avellanea BCC 17816. Tetrahedron 66: 955–961. Jarikhuan, S. (2002). Thraustochytrids: a new alternative sorcesource of fatyfatty acids for aquaculture. In: Hyde, K.D. (Ed.), Fungi in marine environments. Fungal Diversity Press, Hong Kong, pp. 345–357. Jin, J. and Huang, J.G. (2009). The finding of Monosporascus cannonballus in marine environment. Mycosystema 28: 865–869. Jin, J., Li, G.F., Li, B.H., Zhang, T.Y., Liang, C., and Li, B.D. (2004a). Woodinhabiting marine fungi from the coast of Shandong I. Mycosystema 23: 211–215. Jin, J., Wang, Y.L., Zhang, T.Y., and Li, B.D. (2004b). New report of a marine basidiomycetous fungus from China. Mycosystema 23: 599–600. Jin, J., Li, G.F., Zhang, T.Y., and Li, B.D. (2005). New report of marine higher fungi from the Yellow Sea, China I. Mycosystema 24: 336–339. Johanson, C.J. (1884). Svampar på island. Öfvers. K. VetenskAkad. Förh. 41: 157–174. Johnson, R.A. and McNeil, F.A. (1941). Destruction of timber by marine organisms in the Port of Sydney. Supplementary Report No. 2, Maritime Services Board of NS Wales 36. Johnson, T.W., Jr. (1958). Some lignicolous marine fungi from the North Carolina coast. J. Elisha Mitchell Sci. Soc. 74: 42–48. Jones, E.B.G. (1962). Marine fungi. Trans. Br. Mycol. Soc. 45: 93–114. Jones, E.B.G. (1968). Marine fungi. Curr. Sci. 37: 378–379. Jones, E.B.G. (1971). The ecology and rotting ability of marine fungi. In: Jones, E.B.G. (Ed.), Marine borers, fungi and fouling organisms of wood. O.E.C.D., Paris, pp. 237–258. Jones, E.B.G. (1995). Ultrastructure and taxonomy of the aquatic ascomycetous order Halosphaeriales. Can. J. Bot. 73: 790–801. Jones, E.B.G. (2010). Fungi. In: Relini, G. (Ed.). Checklist of the flora and fauna in Italian seas. Biol. Mar. Mediterr. 17: 681–684. Jones, E.B.G. (2011). Are there more marine fungi to be described? Bot. Mar. 54: 343–354. Jones, E.B.G. and Agerer, R. (1992). Calathella mangrovei sp. nov. and observations on the mangrove fungus Halocyphina villosa. Bot. Mar. 35: 259–265. Jones, E.B.G. and Alias, S.A. (1996). Mangrove fungi-biodiversity, biogeography, biotechnological application. In: Wakase, T. and Takeo, K. (Eds.), Proceedings of the Asian international mycological Congress. Chiba, Japan, pp. 1–4. Jones, E.B.G. and Kuthubutheen, A.J. (1989). Malaysian mangrove fungi. Sydowia 41: 160–169. Jones, E.B.G. and Tan, T.K. (1987). Observations on manglicolous fungi from Malaysia. Trans. Br. Mycol. Soc. 89: 390–392. Jones, E.B.G., Kuhne, H., Trussell, P.C., and Turner, R.D. (1972). Results of an international co-operative research programme on the biodeterioration of timber submerged in the sea. Mater. Org. 7: 93–118. Jones, E.B.G., Turner, R.T., Furtado, S.E.G., and Kühne, H. (1976). Marine biodeterioration organisms: lignicolous fungi and bacteria and the wood boring Mollusca and Crustaceae. Int. Biodeterior. Bull. 12: 120–134. Jones, E.B.G., Moss, S.T., and Cuomo, V. (1983). Spore appendage development in the lignicolous marine pyrenomycetes Chaetosphaeria chaetosa and Halosphaeria trullifera. Trans. Br. Mycol. Soc. 80: 193–200. Jones, E.B.G., Uyenco, F.R., and Follosco, M.P. (1988). Fungi on driftwood collected in the intertidal zone from the Philippines. Asian Mar. Biol. 5: 103–106. Jones, E.B.G., Hyde, K.D., Read, S.J., Moss, S.T., and Alias, S.A. (1996). Tirisporella gen. nov., an ascomycete from the mangrove palm Nypa fruticans. Can. J. Bot. 74: 1487–1495. Jones, E.B.G., Pilantanapak, A., Chatmala, I., Sakayaroj, J., Phongpaichit, S., and Choeyklin, R. (2006). Thai marine fungal diversity. Songklanakarin J. Sci. Technol. 28: 687–708. K.-L. Pang et al.: Country reports of marine mycological research Jones, E.B.G., Hyde, K.D., and Vikineswary, S. (2007). Malaysian fungal diversity. Mushroom Research Centre, University of Malaya and Ministry of Natural Resources and Environment, Malaysia. Jones, E.B.G., Sakayaroj, J., Suetrong, S., Somrithipol, S., and Pang, K.L. (2009). Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Divers. 35: 1–187. Jones, E.B.G., Suetrong, S., Bahkali, A.H., Abdel-Wahab, M.A., Boekhout, T., and Pang, K.L. (2015). Classification of marine Ascomycota, Basidiomycota, Blastocladiomycota and Chytridiomycota. Fungal Divers. 3: 1–72. Jones, E.B.G., Ju, W.T., Lu, C.L., Guo, S.Y., and Pang, K.L. (2017). The Halosphaeriaceae revisited. Bot. Mar. 60: 453–468. Jones, E.B.G., Pang, K.L., Abdel-Wahab, M.A., Scholz, B., Hyde, K.D., Boekhout, T., Ebel, R., Rateb, M., Henderson, L., Sakayaroj, J., et al. (2019). An online resource for marine fungi. Fungal Divers. 96: 347–433. Jones, E.B.G., Bandarupalli, D., Abdel-Wahab, M.A., Dayarathne, C., Zhang, S.-N., Hyde, K.D., Liu, J.K., Bahkali, A.N., Sarma, V.V., Tibell, S., et al. (2020). Phylogeny of new marine Dothideomycetes and Sordariomycetes from mangroves and deep-sea sediments. Bot. Mar. 63: 155–181. Juel, H.O. (1901). Pyrrhosorus. Eine neue marine Pilzgattung. Bih. K. Svenska Vet.-Akad. Handl. 26(14): 1–16. Keeler, E., Burgaud, G., Teske, A., Beaudoin, D., Mehiri, M., Dayras, M., and Edgcomb, V. (2021). Deep-sea hydrothermal vent sediments reveal diverse fungi with antibacterial activities. FEMS Microbiol. Ecol. 97: fiab103. Kendrick, B., Risk, M.J., Michaelides, J., and Bergman, K. (1982). Amphibious microborers: bioeroding fungi isolated from live corals. Bull. Mar. Sci. 32: 862–867. Kerzaon, I., Pouchus, Y.F., Monteau, F., Le Bizec, B., Nourrisson, M.R., Biard, J.F., and Grovel, O. (2009). Structural investigation and elucidation of new communesins from a marine‐derived Penicillium expansum Link by liquid chromatography/electrospray ionization mass spectrometry. RCM 23: 3928–3938. Khan, S.S. and Manimohan, P. (2011). Diversity and abundance of marine fungi on driftwood collected from Kerala State and Lakshadweep Island, India. Mycosphere 2: 223–229. Kirk, P. and Spooner, B. (1984). An account of the fungi of Arran, Gigha and Kintyre. Kew Bull. 38: 503–597. Klawonn, I., Van den Wyngaert, S., Parada, A.E., Arandia-Gorostidi, N., Whitehouse, M.J., Grossart, H.P., and Dekas, A.E. (2021). Characterizing the “fungal shunt”: parasitic fungi on diatoms affect carbon flow and bacterial communities in aquatic microbial food webs. PNAS 118: e2102225118. Koch, J. (1986). Some lignicolous marine fungi from Thailand, including two new species. Nord. J. Bot. 6: 497–499. Kohlmeyer, J. (1959). Neufunde hazberrede Inder meerspilze. Nova Hedwigia 1: 77–99. Kohlmeyer, J. (1966). Neue Meerespilze an mangroven. Ber. Dtsch. Bot. Ges. 79: 27–37. Kohlmeyer, J. (1968). Marine fungi from the tropics. Mycologia 60: 252–270. Kohlmeyer, J. (1972). Parasitic Haloguignardia oceanica (ascomycetes) and hyperparasitic Sphaceoma cecidii sp. nov. (Deuteromycetes) in drift Sargassum in North Carolina. J. Elisha Mitchell Sci. Soc. 88: 255–258. Kohlmeyer, J. (1973a). Chadefaudia balliae sp. nov. (Ascomycetes) on Ballia in Australia. Mycologia 65: 244–248. Kohlmeyer, J. (1973b). Fungi from marine algae. Bot. Mar. 16: 201–215. Kohlmeyer, J. (1984). Tropical marine fungi. P.S.Z.N.I. Mar. Ecol. 5: 329–378. 263 Kohlmeyer, J. (1986). Ascocratera manglicola gen. et sp. nov. and key to the marine Loculoasomycetes on mangroves. Can. J. Bot. 64: 3036–3042. Kohlmeyer, J. and Kohlmeyer, E. (1964). Synoptic plates of higher marine fungi, 2nd ed. Cramer, Weinheim. Kohlmeyer, J. and Kohlmeyer, E. (1971). Synoptic plates of higher marine fungi. An identification guide for the marine environment, 3rd ed. Cramer, Lehre. Kohlmeyer, J. and Kohlmeyer, E. (1979). Marine mycology. The higher fungi. Academic Press, New York. Kohlmeyer, J. and Vittal, B.P.R. (1986). Lophiostoma mangrovis, a new marine ascomycete from the tropics. Mycologia 78: 485–489. Kohlmeyer, J. and Volkmann-Kohlmeyer, B. (1987). Marine fungi from Belize, with a description of two new genera of ascomycetes. Bot. Mar. 30: 195–204. Kohlmeyer, J. and Volkmann-Kohlmeyer, B. (1989). Hawaiian marine fungi, including two new genera of Ascomycotina. Mycol. Res. 92: 410–421. Kohlmeyer, J. and Volkmann-Kohlmeyer, B. (1991). Marine fungi of Queensland, Australia. Aust. J. Mar. Freshw. Res. 42: 91–99. Kohlmeyer, J. and Volkmann-Kohlmeyer, B. (2001). The biodiversity of fungi on Juncus roemerianus. Mycol. Res. 105: 1409–1412. Kohlmeyer, J., Schmidt, I., and Nair, N.B. (1967). Eine neue Corollospora (Ascomycetes) aus dem Indischen Ozean and der Ostsee. Ber. Deutsch. Bot. Ges. 80: 98–102. Kohlmeyer, J., Volkmann-Kohlmeyer, B., and Eriksson, O.E. (1995a). Fungi on Juncus roemerianus 2. New dictyosporous ascomycetes. Bot. Mar. 38: 165–174. Kohlmeyer, J., Volkmann-Kohlmeyer, B., and Eriksson, O.E. (1995b). Fungi on Juncus roemerianus 3. New ascomycetes. Bot. Mar. 38: 175–186. Kohlmeyer, J., Volkmann-Kohlmeyer, B., and Eriksson, Ο.Ε. (1995c). Fungi on Juncus roemerianus. 4. New marine ascomycetes. New Ascomycetes. Mycologia 87: 532–542. Kohlmeyer, J., Volkmann-Kohlmeyer, B., and Eriksson, Ο.Ε. (1996). Fungi on Juncus roemerianus. New marine and terrestrial ascomycetes. Mycologia 100: 393–404. Kohlmeyer, J., Volkmann-Kohlmeyer, B., and Eriksson, Ο.Ε. (1997). Fungi on Juncus roemerianus 9. New obligate and facultative marine Ascomycotina. Bot. Mar. 40: 291–300. Kohlmeyer, J., Volkmann-Kohlmeyer, B., and Eriksson, Ο.Ε. (1998). Fungi on Juncus roemerianus. 11. More new ascomycetes. Can. J. Bot. 76: 467–477. Kohlmeyer, J., Spatafora, J.W., and Volkmann-Kohlmeyer, B. (2000). Lulworthiales, a new order of marine Ascomycota. Mycologia 92: 453–458. Krishnaswamy, A. (2019). Proteomic approach to study fungal growth under simulated deep-sea conditions, Ph.D. thesis. Goa, Goa University. Kumar, A., Sorensen, J.L., Hansen, F., Arvas, M., Syed, M.F., Hassan, L., Benz, J.P., Record, E., Henrissat, B., Pöggeler, S., et al. (2018). Genome Sequencing and analyses of two marine fungi from the North Sea unraveled a plethora of novel biosynthetic gene clusters. Sci. Rep. 8: 10187. Kumaresen, V. and Suryanarayanan, T.S. (2002). Endophyte assemblage in young, mature and senescent leaves of Rhiziphora apiculata: evidence for the role of endophytes in mangrove litter degradation. Fungal Divers. 9: 82–91. Kuthubutheen, A.J. (1981). Fungi associated with the aerial parts of Malaysian mangrove plants. Mycopathologia 76: 33–43. Landreau, A., Pouchus, Y.F., Sallenave-Namont, C., Biard, J.F., Boumard, M.C., Robiou du Pont, T., Mondeguer, F., Goulard, C., and Verbist, J.F. (2002). Combined use of LC/MS and a biological test for rapid 264 K.-L. Pang et al.: Country reports of marine mycological research identification of marine mycotoxins produced by Trichoderma koningii. J. Microbiol. Meth. 48: 181–194. Langdon, J.S. and McDonald, W.L. (1987). Cranial Exophiala pisciphila infection in Salmo salar in Australia. Bull. Eur. Assoc. 7: 35–37. Le Calvez, T., Burgaud, G., Mahé, S., Barbier, G., and Vandenkoornhuyse, P. (2009). Fungal diversity in deep-dea hydrothermal ecosystems. Appl. Environ. Microbiol. 75: 6415–6421. Lee, S.S., Alias, S.A., Jones, E.B.G., Zainuddin, N., and Chan, H.T. (2012). Checklist of fungi of Malaysia. Malayan Forest Records. Research Pamphlet no. 132, pp. 1–556. Li, G.J., Hyde, K.D., Zhao, R.L., Hongsanan, S., Abdel-Aziz, F.A., Abdel-Wahab, M.A., Alvarado, P., Alves-Silva, G., Ammirati, S.F., Ariyawansa, H.A., et al. (2016). Fungal diversity notes 253–366: taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers. 78: 1–237. Li, W., Wang, M., Burgaud, G., Yu, H., and Cai, L. (2019). Fungal community composition and depth-related driving factors impacting distribution pattern and trophic modes from epi-to abyssopelagic zones of the Western Pacific Ocean. Microb. Ecol. 78: 820–831. Limtong, S., Kaewwichian, R., Am-In, S., Boonmark, C., Jindamorakot, S., Yongmanitchai, W., Srisuk, N., Kawasaki, H., and Nakase, T. (2010). Three anamorphic yeast species Candida sanitii sp. nov., Candida sekii sp. nov., and Candida suwanaritii, three novel yeasts in the Saturispora clade isolated in Thailand. FEMS Yeast Res. 10: 114–122. Lin, Y.C., Wu, X.Y., Feng, S.A., Jiang, G.C., Zhou, S.N., Vrijmoed, L.L.P., and Jones, E.B.G. (2001a). A novel N-cinnamoylcyclopeptide containing an allenic ether from the fungus Xylaria sp. (strain #2508) from the South China Sea. Tetrahedron Lett. 42: 449–451. Lin, Y.C., Wu, X.Y., Feng, S., Jiang, G.C., Luo, J.H., Zhou, S.N., Vrijmoed, L.L.P., Jones, E.B.G., Krohn, K., Steingröver, K., et al. (2001b). Five unique compounds: xyloketals from mangrove fungus Xylaria sp. from the South China Sea. J. Org. Chem. 66: 6252–6256. Lin, Y.C., Wang, J., Zhou, S.N., and Jones, E.B.G. (2001c). New isocoumarins from the mangrove endophytic fungus #2533. Chem. J. Internet 3: 30. Lin, Y.C., Li, H.J., Jiang, G.C., Zhou, S.N., Vrijmoed, L.L.P., and Jones, E.B.G. (2002a). A novel gamma-lactone, eutypoid-A and other metabolites from marine fungus Eutypa sp. (#424) from the South China Sea. Indian J. Chem. Sect. B. 41: 1542–1544. Lin, Y.C., Wang, J., Wu, X.Y., Zhou, S.N., Vrijmoed, L.L.P., and Jones, E.B.G. (2002b). A novel compound enniatin G from the mangrove fungus Halosarpheia sp. (strain #732) from the South China Sea. Aust. J. Chem. 55: 225–227. Liu, W.C., Li, C.Q., Zhu, P., Yang, J.L., and Cheng, K.D. (2010). Phylogenetic diversity of culturable fungi associated with two marine sponges: Haliclonasimulans and Gelliodescarnosa, collected from the Hainan Island coastal waters of the South China Sea. Fungal Divers. 42: 1–15. Liu, J.K., Hyde, K.D., Jones, E.B.G., Ariyawansa, H.A., Bhat, D.J., Boonmee, S., Maharachchikumbura, S.S.N., McKenzie, E.H.C., Phookamsak, R., Phukhamsakda, C., et al. (2015). Fungal diversity notes 1–110: taxonomic and phylogenetic contributions to fungal species. Fungal Divers. 72: 1–197. Loilong, A., Sakayaroj, J., Rungjindamai, N., Choeyklin, R., and Jones, E.B.G. (2012). Biodiversity of fungi on the palm Nypa fruticans. In: Jones, E.B.G. and Pang, K.L. (Eds.), Marine fungi and fungal-like organisms. De Gruyter, Berlin/Boston, 273–290. Lorenz, R. and Molitoris, H.P. (1997). Cultivation of fungi under simulated deep sea conditions. Mycol. Res. 101: 1355–1365. Lundquist, N. (1969). Tripterospora (Sordariaceae s. lat., pyrenomycetes). Bot. Notiser 122: 589–603. Lundström-Eriksson, A. and Norkrans, B. (1968). Studies on marine occurring yeasts: relations to inorganic nitrogen compounds, especially hydroxylamine. Arch. Microbiol. 62: 373–383. Maamar, A., Lucchesi, M.E., Debaets, S., Nguyen van Long, N., Quemener, M., Coton, E., Burgaud, G., and Matallah-Boutiba, A. (2020). Highlighting the crude oil bioremediation potential of marine fungi isolated from the Port of Oran (Algeria). Diversity 12: 196. Malloch, B., Kernaghan, G., and Walker, A.K. (2022). Temporal diversity patterns for fungi and mites associated with decaying Sporobolus pumilus (Spartina patens) in the Minas Basin, Nova Scotia. FACETS 7: 654–673. Manohar, C.S. and Raghukumar, C. (2013). Fungal diversity from various marine habitats deduced through culture-independent studies. FEMS Microbiol. Lett. 341: 69–78. Mansfield, S.D. and Bärlocher, F. (1993). Seasonal variation of fungal biomass in the sediment of a salt marsh in New Brunswick. Microb. Ecol. 26: 37–45. Marchese, P., Garzoli, L., Gnavi, G., O’Connell, E., Bouraoui, A., Mehiri, M., and Varese, G.C. (2020). Diversity and bioactivity of fungi associated with the marine sea cucumber Holothuria poli: disclosing the strains potential for biomedical applications. J. Appl. Microbiol. 129: 612–625. Maria, G.L. and Sridhar, K.R. (2002). A new ascomycete, Passeriniella mangrovei sp. nov. from the mangrove forest of India. Indian J. For. 25: 319–322. Maria, G.L. and Sridhar, K.R. (2003). Diversity of filamentous fungi on woody litter of five mangrove plant species from the south west coast of India. Fungal Divers. 14: 109–126. Maria, G.L., Sridhar, K.R., and Raviraja, N.S. (2005). Antimicrobial and enzyme activity of mangrove endophytic fungi of S.W. coast of India. J. Agric. Technol. 1: 67–80. McCarthy, P.M. (1991). Notes on Australian Verrucariaceae (lichens). Muelleria 7: 317–332. McCarthy, P.M. (1994). Notes on Australian Verrucariaceae (lichenised ascomycotina). Muelleria 8: 269–273. McCarthy, P.M. (2001). Verrucaria. Flora of Australia, Vol. 58A. Australian Biological Resources Study/CSIRO Publishing, Victoria. McCarthy, P.M. (2008). A new species and new combination of Australian Verrucariaceae. Austr. Lichenol. 63: 17–18. McCarthy, P.M. and Kantvilas, G. (2015). Verrucaria alborimosa, a new maritime lichen from Flinders Island, Tasmania. Muelleria 34: 55–58. Meyers, S.P. (1974). Contribution of fungi to biodegradation of Spartina and other brackish marshland vegetation. Veroeff. Inst. Meeresforsch. Bremerhaven Suppl. 5: 357–375. Meyers, S.P. and Reynolds, E.S. (1957). Incidence of marine fungi in relation to wood-borer attack. Science 126: 969. Meyers, S.P. and Reynolds, E.S. (1959). Cellulolytic activity in lignicolous marine ascomycetes. Bull. Mar. Sci. 9: 441–455. Miller, J.D. and Savard, M.E. (1989). Antibiotic activity of the marine fungus Leptosphaeria oraemaris. Proc. Nova Scotia Inst. Sci. 39: 51–58. Miller, J.D. and Whitney, N.J. (1981a). Fungi from the Bay of Fundy I: lignicolous marine fungi. Can. J. Bot. 59: 1128–1133. Miller, J.D. and Whitney, N.J. (1981b). Fungi from the Bay of Fundy II. Observations on fungi from living and cast seaweeds. Bot. Mar. 24: 405–412. Miller, J.D. and Whitney, N.J. (1981c). Fungi of the Bay of Fundy III. Geofungi in the marine environment. Mar. Biol. 65: 61–68. Miller, J.D. and Whitney, N.J. (1981d). Fungi of the Bay of Fundy IV. Thraustochytrids. Nova Hedwigia 35: 407–416. K.-L. Pang et al.: Country reports of marine mycological research Miller, J.D. and Whitney, N.J. (1983). Fungi of the Bay of Fundy V. Fungi from living species of Spartina Schreber. Proc. Nova Scotian Inst. Sci. 33: 75–83. Miller, J.D., Moharir, Y.E., Findlay, J.A., and Whitney, N.J. (1984). Marine fungi of the Bay of Fundy VI. Growth and metabolites of Leptoshpaeria oraemaris, Sphaerulina oraemaris, Monodictys pelagica and Dendryphiella salina. Proc. Nova Scotian Insti. Sci. 34: 1–8. Mitchison-Field, L.M.Y. and Gladfelter, A.S. (2021). Culturing and multiplexed time-lapse imaging of fungal isolates from marine and coastal environments. Curr. Protoc. 1: e94. Mitchison-Field, L.M.Y., Vargas-Muñiz, J.M., Stormo, B.M., Vogt, E.J.D., Van Dierdonck, S., Pelletier, J.F., Ehrlich, C., Lew, D.J., Field, C.M., and Gladfelter, A.S. (2019). Unconventional cell division cycles from marine-derived yeasts. Curr. Biol. 29: 3439–3456. Montermartini Corte, A. (1975). Observazione sui genere Lulworthia Suth. e sui suoi rapport con Limnoria Menzies e segna-lazione di alter specie. Giorn. Bot. Ital. 109: 227–237. Montermartini Corte, A. (1979). La microflora marina della Baia di Portefino. Giorn. Bot. Ital. 113: 297–325. Morehouse, N.J., Flewelling, A.J., Johnson, J.A., and Gray, C.A. (2020). Halogenated Bianthrones from Penicillium roseopurpureum: a fungal endophyte of the marine alga Petalonia fascia. Nat. Prod. Comm. 15: 1934578X20901405. Nair, N.B. (1970). The problem of timer destroying organisms along the Indian coast. In: Proceedings, 2nd International congress of marine corrosion and fouling 1968. Technical Chamber of Greece, Atenas, pp. 1–7. Nambiar, G., Raveendran, K., and Jaleel, C.A. (2009). Marine mycoflora of south India with special emphasis to lignicolous marine fungi. Front. Biol. 4: 436–441. Nambiar, G. and Raveendran, K. (2010). Frequency and abundance of algicolous marine fungi along Indian coast. Seaweed Res. Utlin. 30: 1–5. Nambiar, G. and Raveendran, K. (2015). Frequency of marine fungi on animal substrates along west coast of India. Curr. Res. Environ. Appl. Mycol. 5: 394–397. Nannfeldt, J.A. (1932). Studien über die morphologie und systematik der nicht-lichenisierten inoperculatn discomyceten. Nova Acta Regiae Soc. Sci. Upsaliensis 8: 190. Neish, G.A. (1970). Lignicolous marine fungi from Nova Scotia. Can. J. Bot. 48: 2319–2322. Newell, S.Y. (1993). Membrane-containing fungal mass and fungal specific growth rate in natural samples. In: Kemp, P.F., Cole, J.J., Sherr, B.F., and Sherr, E.B. (Eds.), Handbook of methods in aquatic microbial ecology. CRC Press, Boca Raton, pp. 579–586. Newell, S.Y., Miller, J.D., and Fallon, R.D. (1987). Ergosterol content of saltmarsh fungi: effect of growth conditions and mycelial age. Mycologia 79: 688–695. Nilsson, S. (1964). Freshwater hyphomycetes. Symb. Bot. Upsal. 21: 1–130. Nilsson, S. (1971). Validation of aquatic hyphomycete names. Trans. Br. Mycol. Soc. 57: 531–542. Norton, J.H., Thomas, A.D., and Barker, J.R. (1994). Fungal infection in the cultured juvenile boring clam Tridacna crocea. J. Invertebr. Pathol. 64: 273–275. Nour El-Din, A.A.H. (2022). Diversity of aquatic fungi in Qaroun Lake, M.Sc. thesis. Sohag, Sohag University. Nour El-Din, A.A.H., Abdel-Aziz, F.A., and Abdel-Wahab, M.A. (2022). Qarounispora grandiappendiculata gen. et sp. nov. (Halosphaeriaceae, Microascales) from Qaroun Lake, Egypt. Phytotaxa 530: 86–94. 265 Oppong-Danquah, E., Parrot, D., Blumel, M., Labes, A., and Tasdemir, D. (2018). Molecular networking-based metabolome and bioactivity analyses of marine-adapted fungi co-cultivated with phytopathogens. Front. Microbiol. 9: 2072. Orsi, W.D., Richards, T.A., and Francis, W.R. (2018). Predicted microbial secretomes and their target substrates in marine sediment. Nat. Microbiol. 3: 32–37. Orsi, W.D., Vuillemin, A., Coskun, O.K., Rodriguez, P., Oertel, Y., Niggemann, J., Mohrholz, V., and Gomez-Saez, G.V. (2022). Carbon assimilating fungi from surface ocean to subseafloor revealed by coupled phylogenetic and stable isotope analysis. ISME J. 16: 1245–1261. Overy, D.P., Berrue, F., Correa, H., Hanif, N., Hay, K., Lanteigne, M., Mquilian, K., Duffy, S., Boland, P., Jagannathan, R., et al. (2014). Sea foam as a source of fungal inoculum for the isolation of biologically active natural products. Mycology 5: 130–144. Overy, D.P., Rämä, T., Oosterhuis, R., Walker, A.K., and Pang, K.L. (2019). The neglected marine fungi, Sensu stricto, and their isolation for natural products’ discovery. Mar. Drugs 17: 42. Panebianco, C. (1990). Temperature requirements of selected marine fungi. Bot. Mar. 37: 157–161. Panebianco, C., Tam, W.Y., and Jones, E.B.G. (2002). The effect of preinoculation of balsa wood by selected marine fungi and their effect on subsequent colonisation in the sea. Fungal Divers. 10: 77–88. Pang, K.L. and Jheng, J.S. (2012a). A checklist of marine fungi of Taiwan with a description of Kitesporella keelungensis. gen. et sp. nov. Bot. Mar. 55: 459–466. Pang, K.L. and Jheng, J.S. (2012b). Pileomyces formosanus gen. et sp. nov. (Halosphaeriaceae, Ascomycota) from a rocky shore of Taiwan. Bot. Stud. 53: 535–539. Pang, K.L., Chiang, M.W.L., and Vrijmoed, L.L.P. (2008). Havispora longyearbyenensis gen. et sp. nov.: an arctic marine fungus from Svalbard, Norway. Mycologia 100: 291–295. Pang, K.L., Chiang, M.W.L., and Vrijmoed, L.L.P. (2009). Remispora spitsbergenensis sp. nov. a marine lignicolous ascomycete from Svalbard, Norway. Mycologia 101: 531–534. Pang, K.L., Alias, S.A., Chiang, M.W.L., Vrijmoed, L.L.P., and Jones, E.B.G. (2010a). Sedecimiella taiwanensis gen. et sp. nov., a marine mangrove fungus in the Hypocreales (Hypocreomycetidae, Ascomycota). Bot. Mar. 53: 493–498. Pang, K.L., Sharuddin, S.S., Alias, S.A., Nor, N.A.M., and Awaluddin, H.H. (2010b). Diversity and abundance of lignicolous marine fungi from the east and west coasts of Peninsular Malaysia and Sabah (Borneo Island). Bot. Mar. 53: 515–523. Pang, K.L., Chow, R.K.K., Chan, C.W., and Vrijmoed, L.L.P. (2011a). Diversity and physiology of marine lignicolous fungi in Arctic waters: a preliminary account. Polar Res. 30: 1–5. Pang, K.L., Jheng, J.S., and Jones, E.B.G. (2011b). Marine mangrove fungi of Taiwan. National Taiwan Ocean University Press, Keelung. Pang, K.L., Hyde, K.D., Alias, S.A., Suetrong, S., Guo, S.Y., Rizman-Idid, M., and Jones, E.B.G. (2013). Dyfrolomycetaceae, a new family in the Dothideomycetes, Ascomycota. Cryptogam. Mycol. 34: 223–232. Pang, K.L., Guo, S.Y., Alias, S.A., Hafellner, J., and Jones, E.B.G. (2014). A new species of marine Dactylospora and its phylogenetic affinities within the Eurotiomycetes, Ascomycota. Bot. Mar. 57: 315–321. Pang, K.L., Chen, I.A., Ju, W.T., and Guo, S.Y. (2016). A checklist of marine fungi of Hong Kong. Fung. Sci. 31: 7–17. Pang, K.L., Guo, S.Y., Chen, I.A., Burgaud, G., Luo, Z.H., Dahms, H.U., Hwang, J.S., Lin, Y.L., Huang, J.S., Ho, T.W., et al. (2019). Insights into fungal diversity of a shallow-water hydrothermal vent field at Kueishan 266 K.-L. Pang et al.: Country reports of marine mycological research Island, Taiwan by culture-based and metabarcoding analyses. PloS One 14: e0226616. Pang, K.L., Luo, Z.H., and Burgaud, G. (2020). The 15th international marine and freshwater mycology Symposium (IMFMS). Bot. Mar. 63: 119–120. Panno, L., Bruno, M., Voyron, S., Anastasi, A., Gnavi, G., Miserere, L., and Varese, G.C. (2013). Diversity, ecological role and potential biotechnological applications of marine fungi associated to the seagrass Posidonia oceanica. New Biotechnol. 30: 685–694. Patil, S.D. and Borse, B.D. (1983). Marine fungi from Maharashtra India. III. Some fungi from mangroves. Indian Bot. Reptr. 2: 56–58. Pedersen, M. and Fries, N. (1977). Bromophenols identified in a marine ascomycete and its culture medium. Z. Pflanzenphysiol. 82: 363–366. Pedersen, O.A. and Langvad, F. (1989). Exophiala psychrophila sp. nov., a pathogenic species of the black yeasts isolated from farmed Atlantic salmon. Mycol. Res. 92: 153–156. Philippe, A., Noël, C., Eyheraguibel, B., Briand, J.-F., Paul-Pont, I., Ghiglione, J.-F., Coton, E., and Burgaud, G. (2023). Fungal diversity and dynamics during long-term immersion of conventional and biodegradable plastics in the marine environment. Diversity 15: 579. Phongpaichit, S., Rungjindamai, N., Rukachaisirikul, V., and Sakayaroj, J. (2006). Antimicrobial activity in cultures of endophytic fungi isolated from Garcinia species. FEMS Immunol. Med. Microbiol. 48: 367–372. Phukhamsakda, C., Nilsson, R.H., Bhunjun, C.S., de Farias, A.R.G., Sun, Y.R., Wijesinghe, S.N., Raza, M., Bao, D.F., Lu, L., Tibpromma, S., et al. (2022). The numbers of fungi: contributions from traditional taxonomic studies and challenges of metabarcoding. Fungal Divers. 114: 327–386. Pilantanapak, A., Jones, E.B.G., and Eaton, R.A. (2005). Marine fungi on Nypa fruticans in Thailand. Bot. Mar. 48: 365–373. Poli, A., Bovio, E., Verkley, G., Prigione, V., and Varese, G.C. (2019). Elbamycella rosea gen. et sp. nov. (Juncigenaceae, Torpedosporales) isolated from the Mediterranean Sea. MycoKeys 55: 15–28. Poli, A., Bovio, E., Ranieri, L., Varese, G.C., and Prigione, V. (2020). Fungal diversity in the Neptune Forest: comparison of the mycobiota of Posidonia oceanica, Flabellia petiolata, and Padina pavonica. Front. Microbiol. 11: 15. Poli, A., Bovio, E., Perugini, I., Varese, G.C., and Prigione, V. (2021a). Corollospora mediterranea: a novel species complex in the Mediterranean Sea. Appl. Sci. 11: 14. Poli, A., Prigione, V., Bovio, E., Perugini, I., and Varese, G.C. (2021b). Insights on Lulworthiales inhabiting the Mediterranean Sea and description of three novel species of the genus Paralulworthia. J. Fungi 7: 940. Poli, A., Varese, G.C., Garzoli, L., and Prigione, V. (2022). Seagrasses, seaweeds and plant debris: an extraordinary reservoir of fungal diversity in the Mediterranean Sea. Fungal Ecol. 60: 101156. Portillo-Lopez, A. and Gonzalez-Martinez, S. (2021). Marine fungi from different habitats recorded from 2001 to date in Mexico. J. Microbiol. Exp. 9: 34–37. Prasannarai, K., Ananda, K., and Sridhar, K.R. (2000). Corollospora indica, a new marine fungal species from west coast at India. J. Environ. Biol. 21: 235–239. Priest, T., Fuchs, B., Amann, R., and Reich, M. (2021). Diversity and biomass dynamics of unicellular marine fungi during a spring phytoplankton bloom. Environ. Microbiol. 23: 448–463. Qiao, Q. and Jin, J. (2011). Two new Chinese records of Phaeosphaeria. J. Qingdao Agric. Univers. (Nat. Sci.) 28: 44–46. Quémener, M., Dayras, M., Frotté, N., Debaets, S., Le Meur, C., Barbier, G., Burgaud, G., and Mehiri, M. (2021). Highlighting the biotechnological potential of deep oceanic crust fungi through the prism of their antimicrobial activity. Mar. Drugs 19: 411. Raghukumar, C. (1986). Fungal parasites of the marine green algae, Cladophora and Rhizoclonium. Bot. Mar. 29: 289–298. Raghukumar, C. and Ravindran, J. (2012). Fungi and their role in corals and coral reef ecosystems. In: Raghukumar, C. (Ed.), Biology of marine fungi. Springer, Berlin/Heidelberg, pp. 89–113. Raghukumar, C. and Schaumann, K. (1973). An epifluorescence microscopy method for direct detection and enumeration of the fungilike marine protists, the thraustochytrids. Limnol. Oceanogr. 38: 182–187. Raghukumar, C., Nagarkar, S., and Raghukumar, S. (1992). Association of Thraustochytrids and fungi with living marine algae. Mycol. Res. 96: 542–546. Raghukumar, S. (1973). Marine lignicolous fungi from India. Kavaka 1: 73–85. Raghukumar, S. (2002). Ecology of the marine protists, the Labyrinthulomycetes (thraustochytrids and Labyrinthulids). Eur. J. Protistol. 38: 127–145. Raghukumar, S. (2005). The role of fungi in marine detrital processes. In: Ramaiah, N. (Ed.), Marine microbiology: facets and opportunities. The National Institute of Oceanography, Goa, pp. 91–101. Raghukumar, S. and Damare, V.S. (2011). Increasing evidence for the important role of Labyrinthulomycetes in marine ecosystems. Bot. Mar. 54: 3–11. Rämä, T., Mathiassen, G.H., and Kauserud, H. (2014a). Marine fungi new to Norway, with an outlook to the overall diversity. Agarica 35: 35–47. Rämä, T., Nordén, J., Davey, M.L., Mathiassen, G.H., Spatafora, J.W., and Kauserud, H. (2014b). Fungi ahoy! Diversity on marine wooden substrata in the high North. Fungal Ecol. 8: 46–58. Rämä, T., Hassett, B.T., and Bubnova, E. (2017). Arctic marine fungi: from filaments and flagella to operational taxonomic units and beyond. Bot. Mar. 60: 433–452. Raveendran, K. and Manimohan, P. (Eds.) (2007). Marine fungi of Kerala, a preliminary floristic and ecological study. Malbar Natural History Society, Calicat, Kerala. Ravikumar, D.R. and Vittal, B.P.R. (1991). A new species of Bathyascus from Indian mangroves. Mycol. Res. 95: 370–371. Réblová, M., Miller, A.N., Rossman, A.Y., Seifert, K.A., Crous, P.W., Hawksworth, D.L., Abdel-Wahab, M.A., Cannon, P.F., Daranagama, D.A., De Beer, Z.W., et al. (2016). Recommendations for competing sexual-asexually typified generic names in sordariomycetes (except diaporthales, hypocreales, and magnaporthales). IMA Fungus 7: 131–153. Rédou, V., Ciobanu, M.C., Pachiadaki, M.G., Edgcomb, V., Alain, K., Barbier, G., and Burgaud, G. (2014). In-depth analyses of deep subsurface sediments using 454-pyrosequencing reveals a reservoir of buried fungal communities at record-breaking depths. FEMS Microbiol. Ecol. 90: 908–921. Roth, F.J., Jr., Ahearn, D.G., Fell, J.W., Meyers, S.P., and Meyer, S.A. (1962). Ecology and taxonomy of yeasts isolated from various marine substrates1. Limnol. Oceanogr. 7: 178–185. Roullier, C., Guitton, Y., Valery, M., Amand, S., Prado, S., Robiou du Pont, T., Grovel, O., and Pouchus, Y.F. (2016). Automated detection of natural halogenated compounds from LC-MS profiles–application to the isolation of bioactive chlorinated compounds from marine-derived fungi. Anal. Chem. 88: 9143–9150. Ruiz, N., Wielgosz-Collin, G., Poirier, L., Grovel, O., Petit, K.E., MohamedBenkada, M., Robiou du Pont, T., Bissett, J., Vérité, P., Barnathan, G., et al. (2007). New Trichobrachins, 11-residue peptaibols from a marine strain of Trichoderma longibrachiatum. Peptides 28: 1351–1358. Rukachaisirikul, V., Khamthong, N., Sukpondma, Y., Pakawatchai, C., Phongpaichit, S., Sakayaroj, J., and Kirtikara, K. (2009). An [11] K.-L. Pang et al.: Country reports of marine mycological research cytochalasin derivative from the marine-derived fungus Xylaria sp. PSU-F100. Chem. Pharm. Bull. 57: 1409–1411. Rukachaisirikul, V., Rodglin, A., Phongpaichit, S., Buatong, J., and Sakayaroj, J. (2011). α-Pyrone and seiricuprolide derivatives from the mangrovederived fungi Pestalotiopsis spp. PSU-MA92 and PSU-MA119. Phytochem. Lett. 5: 13–17. Sadaba, R.B. and Sarinas, B.G.S. (2010). Fungal communities in bunker C oilimpacted sites off southern Guimaras, Philippines: a post-spill assessment of Solar 1 oil spill. Bot. Mar. 53: 565–575. Sakayaroj, J., Jones, E.B.G., Chatmala, I., and Phongpaichit, S. (2004). Marine fungi. In: Jones, E.B.G., Tantichareon, M., and Hyde, K.D. (Eds.), Thai fungal diversity. BIOTEC, Bangkok, pp. 107–117. Sallenave-Namont, C., Pouchus, Y.F., Robiou du Pont, T., Lassus, P., and Verbist, J.F. (2000). Toxigenic saprophytic fungi in marine shellfish farming areas. Mycopathologia 149: 21–25. Samadi, S., Corbari, L., Lorion, J., Hourdez, S., Haga, T., Dupont, J., Boisselier, M.C., and Richer De Forges, B. (2010). Biodiversity of deepsea organisms associated with sunken-wood or other organic remains sampled in the tropical Indo-Pacific. Cah. Biol. Mar. 51: 459–466. Samiaji, J. and Bärlocher, F. (1996). Geratology and decomposition of Spartina alterniflora Loisel in a new Brunswick saltmarsh. J. Exp. Mar. Biol. Ecol. 201: 233–252. Sarma, V.V. and Vittal, B.P.R. (1998–1999). Ecological studies on manglicolous fungi from Godavari and Krishna deltas, East coast of India. Observations on the seasonal occurrence. Kavaka 26–27: 105–120. Sarma, V.V. and Vittal, B.P.R. (2000). Biodiversity of mangrove fungi on different substrata of Rhizophora apiculata and Avicennia sp. from Godavari and Krishna deltas, East coast of India. Fungal Divers. 5: 23–41. Sarma, V.V. and Vittal, B.P.R. (2001). Biodiveristy of manglicolous fungi on selected plants in the Godavari and Krishna deltas, East Coast of India. Fungal Divers. 6: 115–130. Sarma, V.V. and Vittal, B.P.R. (2002). A preliminary study on vertical distribution of manglicolous fungi on prop roots of Rhizophora apiculata Blume at Krishna delta, East coast of India. Kavaka 30: 21–29. Sarma, V.V. and Vittal, B.P.R. (2004). Manglicolous fungi recorded from Godavary and Krishna deltas, A. P., East coast of India along with dichotomous key and notes on some taxa. Kavaka 32: 65–111. Sarma, V.V., Raghukumar, S., Hyde, K.D., Vittal, B.P.R., and Chandramohan, D. (2000). A CD-ROM for documentation and identification of mangrove fungi. Fungal Divers. 5: 195–200. Sarma, V.V., Hyde, K.D., and Vittal, B.P.R. (2001). Frequency of occurrence of mangrove fungi from the East coast of India. Hydrobiologia 455: 41–53. Schatz, S. (1985). Adomia avicenniae: a new ascomycetous genus from Red Sea and Australian mangroves. Trans. Br. Mycol. Soc. 84: 555–559. Schaumann, K. (1968). Marine höhere Pilze (Ascomycetes und Fungi imperfecti) aus dem Weser-Ästuar. Veröffentlichungen des Instituts für Meeresforschung Bremerhaven 11: 93–117. Schmidt, I. (1974). Untersuchungen über höhere Meerespilze an der Ostseeküste der DDR. Natur und Naturschutz in Mecklenburg 12: 1–148. Shearer, C.A. and Crane, J.L. (1971). Fungi of the Chesapeake Bay and its tributaries. I. Patuxent river. Mycologia 63: 237–260. Shi, C., Chen, J., Ge, Q., Sun, J., Guo, W., Wang, J., Peng, L., Xu, Q., Fan, G., Zhang, W., et al. (2021). Draft genomes and comparative analysis of seven mangrove rhizosphere-associated fungi isolated from Kandelia obovata and Acanthus ilicifolius. Front. Fungal Biol. 2: 626904. 267 Singh, P., Raghukumar, C., Meena, R.M., Verma, P., and Shouche, Y. (2012). Fungal diversity in deep-sea sediments revealed by culture-dependent and culture-independent approaches. Fungal Ecol 55: 543–553. Spatafora, J.W. and Blackwell, M. (1994). The polyphyletic origins of ophiostomatoid fungi. Mycol. Res. 98: 1–9. Spatafora, J.W., Volkmann-Kohlmeyer, B., and Kohlmeyer, J. (1998). Independent terrestrial origins of the Halosphaeriales (marine Ascomycota). Am. J. Bot. 85: 1569–1580. Sridhar, K.R. and Kaveriappa, K.M. (1988). Occurrence and survival of aquatic hyphomycetes in brackish and seawater. Arch. fur Hydrobiol. 113: 153–160. Sridhar, K.R. and Kaveriappa, K.M. (1991). A note on marine fungi from Mangalore coast. Mahasagar 24: 63–66. Sridhar, K.R., Karamchand, K.S., Pascoal, C., and Cássio, F. (2012). Assemblage and diversity of fungi on wood and seaweed litter of seven northwest Portuguese beaches. Prog. Mol. Subcel. Biol. 53: 209–228. Starbäck, K. (1896). Sphaerulina halophila (Bomm. Rouss. et Sacc.) en parasitisk pyrenomycet [Sphaerulina halophila (Bomm. Rouss. et Sacc.) a parasitic pyrenomycet]. Bihang Svenska Vet Akad Handlingar III: 3–19, (in Swedish). Strongman, D., Miller, J.D., and Whitney, N.J. (1985). Lignicolous marine fungi from Prince Edward Island with a description of Didymosphaeria lignomaris sp. nov. Proc. Nova Scotia Inst. Sci. 35: 99–105. Suetrong, S., Klaysuban, A., Sakayaroj, J., Preedanaon, S., Rungareerate, P., Phongpaichit, S., Pang, K.L., and Jones, E.B.G. (2015). Tirisporellaceae, a new family in the order Diaporthales (Sordariomycetes, Ascomycota). Cryptogam. Mycol. 36: 319–330. Suetrong, S., Preedanon, S., Klaysuban, A., Gundool, W., Unagul, P., Sakayaroj, J., Promchu, W., and Sangtiean, T. (2017). Distribution and occurrence of manglicolous marine fungi from eastern and southern Thailand. Bot. Mar. 60: 503–514. Sun, S.L., Jin, J., Li, B.D., and Lu, B.S. (2008a). Wood–inhabiting marine fungi from the coast of Shandong III. Mycosystema 27: 66–74. Sun, S.L., Jin, J., Li, B.D., Lu, B.S., and Diao, L.G. (2008b). Wood–inhabiting marine fungi from the coast of Shandong, China IV. Buergenerula, a genus new to China. Mycosystema 27: 520–524. Sundari, R. and Vikineswary, S. (2002). The effect of agitation on ascomata formation of the marine ascomycete Corollospora gracilis. In: Hyde, K.D. (Ed.), Fungi in marine environments. Fungal Diversity Press, Hong Kong, 213–233. Sundari, R., Vikineswary, S., and Yusoff, M. (1995). Fungi on driftwood from the sandy beaches of Port Dickson, Malaysia. J. Biosci. 6: 105–107. Sundari, R., Vikineswary, S., Yusoff, M., and Jones, E.B.G. (1996a). Corollospora besarispora, a new arenicolous marine fungus from Malaysia. Mycol. Res. 100: 1259–1262. Sundari, R., Vikineswary, S., Yusoff, M., and Jones, E.B.G. (1996b). Observations on tropical arenicolous marine fungi on driftwood from Malaysia and Singapore. Bot. Mar. 39: 327–334. Supaphon, P., Phongpaichit, S., Sakayaroj, J., Rukachisirkul, V., Kobmoo, N., and Spatafora, J.K. (2017). Phylogenetic community structure of fungal endophytes in seagrass species. Bot. Mar. 60: 489–502. Suryanarayanan, T.S. (2012a). The diversity and importance of fungi associated with marine sponges. Bot. Mar. 55: 553–564. Suryanarayanan, T.S. (2012b). Fungal endosymbionts of seaweeds. In: Raghukumar, C. (Ed.), Biology of marine fungi, Vol. 53. Springer, Berlin/ Heidelberg, pp. 53–69. Suryanarayanan, T.S. and Kumaresan, V. (2000). Endophytic fungi of some halophytes from an estuarine mangrove forest. Mycol. Res. 104: 1465–1467. 268 K.-L. Pang et al.: Country reports of marine mycological research Suryanarayanan, T.S., Ambayeram, V., Thirunavukkarasu, N., Ravishankar, P., Doble, M., and Geetha, V. (2010). Internal mycobiota of marine macroalgae from the Tamilnadu coast: distribution, diversity and biotechnology potential. Bot. Mar. 53: 457–468. Sutherland, G.K. (1915). New marine fungi on Pelvetia. New Phytol. 14: 33–42. Sutherland, G.K. (1916). Additional nots on marine Pyrenomycetes. Trans. Brit. Mycol. Soc. 5: 257–263. Taylor, V., Adams, S., Robicheau, B.M., and Walker, A.K. (2022). Fungal planet description sheet 1417: Lulworthia fundyense. Persoonia 48: 330–331. Tibell, S. (2016). New records of marine fungi from Sweden. Svensk Mykologisk Tidskrift 37: 43–54. Tibell, S., Tibell, L., Pang, K.L., and Jones, E.B.G. (2019). A conspectus of the filamentous marine fungi of Sweden. Bot. Mar. 63: 141–153. Tibell, S., Tibell, L., Pang, K.L., Calabon, M., and Jones, E.B.G. (2020). Marine fungi of the Baltic sea. Mycology 11: 195–213. Tisthammer, K.H., Cobian, G.M., and Amend, A.S. (2016). Global biogeography of marine fungi is shaped by the environment. Fungal Ecol. 19: 39–46. Torres, J.M., Cardenas, C., Moron, L., Guzman, A., and Dela Cruz, T.E. (2012). Dye decolorization activities of marine-derived fungi isolated from Manila Bay and Calatagan Bay, Philippines. Philippine J. Sci. 140: 133–143. Tourneroche, A., Lami, R., Burgaud, G., Domart-Coulon, I., Li, W., Gachon, C., Gèze, M., Bœuf, D., and Prado, S. (2020). The bacterial and fungal microbiota of Saccharina latissima (Laminariales, Phaeophyceae). Front. Mar. Sci. 7: 587566. Trisuwan, K., Rukachaisirikul, V., Sukpondma, Y., Preedanon, S., Phongpaichit, S., and Sakayaroj, J. (2009). Pyrone derivatives from the marine-derived fungus Nigrospora sp. PSU-F18. Phytochem 70: 554–557. Trisuwan, K., Rukachaisirikul, V., Preedanon, S., Phongpaichit, S., and Sakayaroj, J. (2011). Modiolide and Pyrone derivatives from the sea fan-derived fungus Curvularia sp. PSU-F22. Arch. Pharm. Res. 34: 709–714. Trussell, P.C. and Jones, E.B.G. (1970). Protection of wood in the marine environment. Int. Biodeterior. Bull. 6: 3–7. Ulken, A. (1970). Phycomycetes aus der Mangrove bei Cananeia (Sao Paulo, Brasilien). Veröff. Inst. Meeresf. Bremerhaven 12: 313–319. Ulken, A. (1972). Physiological studies on a Phycomycete from a mangrove swamp at Canananeia, Sao Paulo, Brazil. Veröff. Inst. Meeresf. Bremerhaven 13: 217–230. Unagul, P., Suestron, S., Preedanon, S., Klaysuban, A., Gundool, W., Surlyachadkun, C., and Sakayaroj, J. (2017). Isolation, fatty acid profiles and cryopreservation of marine thraustochytrids from mangrove habitats in Thailand. Bot. Mar. 60: 363–380. Vail, C.A. and Walker, A.K. (2021). Vertical zonation of some crustose lichens (Verrucariaceae) in Bay of Fundy littoral zones of Nova Scotia. Northeast. Nat. 28: 311–326. Vallet, M., Strittmatter, M., Murúa, P., Lacoste, S., Dupont, J., Hubas, C., Genta-Jouve, G., Gachon, C., Kim, G.H., and Prado, S. (2018). Chemically-mediated interactions between macroalgae, their fungal endophytes, and protistan pathogens. Front. Microbiol. 9: 3161. Vallet, M., Meziane, T., Thiney, N., Prado, S., and Hubas, C. (2020). Laminariales host does impact lipid temperature trajectories of the fungal endophyte Paradendryphiella salina (Sutherland). Mar. Drugs 18: 379. van Bohemen, A.I., Ruiz, N., Zalouk-Vergnoux, A., Michaud, A., Robiou du Pont, T., Druzhinina, I., Atanasova, L., Prado, S., Bodo, B., Meslet-Cladiere, L., et al. (2021). Pentadecaibins I-V: 15-residue peptaibols produced by a marine-derived Trichoderma sp. of the harzianum clade. J. Nat. Prod. 84: 1271–1282. Vansteelandt, M., Kerzaon, I., Blanchet, E., Tankoua, O.F., Robiou du Pont, T., Joubert, Y., Monteau, F., Le Bizec, B., Frisvad, J.C., Pouchus, Y.F., et al. (2012). Patulin and secondary metabolite production by marinederived Penicillium strains. Fungal Biol. 116: 954–961. Vansteelandt, M., Blanchet, E., Egorov, M., Petit, F., Toupet, L., Bondon, A., Monteau, F., Le Bizec, B., Thomas, O.P., Pouchus, Y.F., et al. (2013). Ligerin, an antiproliferative chlorinated sesquiterpenoid from a marine-derived Penicillium strain. J. Nat. Prod. 76: 297–301. Velez, P., González, M.C., Rosique-Gil, E., Cifuentes, J., Reyes-Montes, M.R., Capello-García, S., and Hanlin, R.T. (2013). Community structure and diversity of marine ascomycetes from coastal beaches of southern Gulf of Mexico. Fungal Ecol. 6: 513–521. Velez, P., González, M.C., Capello-García, S., Rosique-Gil, E., and Hanlin, R.T. (2015). Diversity of marine ascomycetes from the disturbed sandy beaches of Tabasco, Mexico. J. Mar. Biol. Assoc. UK 95: 897–903. Venkatachalam, A., Thirunavukkarasu, N., and Suryanarayanan, T.S. (2015). Distribution and diversity of endophytes in seagrasses. Fungal Ecol. 13: 60–65. Vittal, B.P.R. and Sarma, V.V. (2006). Diversity and ecology of fungi on mangroves of Bay of Bengal region – an overview. Indian J. Mar. Sci. 35: 308–317. Volz, P.A., Hsu, Y.C., and Liu, C.H. (1976). The Thraustochytriaceae and other intertidal fungi of Taiwan. Taiwania 21: 1–5. Vrijmoed, L.L.P. (1983). Physiological studies on marine lignicolous fungi with special references to their nutrition, germination and wood degrading activities, Ph.D. thesis. Hong Kong, University of Hong Kong. Vrijmoed, L.L.P. and Jones, E.B.G. (1993). Observations on subtropical mangrove fungi. In: Issac, S., Frankland, J.C., Watling, R., and Whalley, A.J.S. (Eds.), Aspects of tropical mycology. Cambridge University Press, Cambridge, p. 310. Vrijmoed, L.L.P., Jones, E.B.G., and Alias, S.A. (1996). Preliminary observations on marine fungi and mangrove fungi from Hainan Island in South China Sea. Asian J. Trop. Biol. 2: 31–36. Wainwright, B.J., Zahn, G.L., Spalding, H.L., Sherwood, A.R., Smith, C.M., and Amend, A.S. (2017). Fungi associated with mesophotic macroalgae from the ‘Au‘au Channel, west Maui are differentiated by host and overlap terrestrial communities. PeerJ 5: e3532. Walker, A.K. and Campbell, J. (2010). Marine fungal diversity: a comparison of natural and created salt marshes of the north-central Gulf of Mexico. Mycologia 102: 513–521. Wang, M.M., Li, C.L., Sun, K.M., Pan, H.Q., and Li, W. (2016). Three new records of endophytic fungi isolated from marine algae in China. Mycosystema 35: 636–640. Wang, M.M., Shenoy, B.D., Li, W., and Ca, L. (2017). Molecular phylogeny of Neodevriesia, with two new species and several new combinations. Mycologia 109: 965–974. Wang, M., Ma, Y., Cai, L., Tedersoo, L., Bahram, M., Burgaud, G., Li, W., and Zhang, S. (2021). Seasonal dynamics of mycoplankton in the Yellow Sea reflect the combined effect of riverine inputs and hydrographic conditions. Mol. Ecol. 30: 3624–3637. Werdermann, E. (1922). Corollospora maritima Werd., ein salzliebender Pilz von der Nordseeküste. Notizblatt des Königlichen Botanischen Gartens und Museums zu Berlin 73: 248–250. Wijesinghe, S.N., Calabon, M.S., Xiao, Y., Jones, E.B.G., and Hyde, K.D. (2023). A novel coniothyrium-like genus in Coniothyriaceae (Pleosporales) from salt marsh ecosystems in Thailand. Stud. Fungi 9: 6. Wilson, I.M. (1954). Ceriosporopsis halima Linder and Ceriosporopsis cambrensis sp. nov. two Pyrenomycetes on wood. Trans. Brit. Mycol. Soc. 37: 272–285. Wilson, I.M. (1956). Some new marine Pyrenomycetes on wood and rope: Halophiobolus and Lindra. Trans. Brit. Mycol. Soc. 39: 401–415. K.-L. Pang et al.: Country reports of marine mycological research Wu, K., Liu, Y., Liao, X., Yang, X., Chen, Z., Mo, L., Zhong, S., and Zhang, X. (2023). Fungal diversity and its relationship with environmental factors in coastal sediments from Guangdong, China. J. Fungi 9: 101. Wurzbacher, C., Larsson, E., Bengtsson-Palme, J., Van den Wyngaert, S., Svantesson, S., Kristiansson, E., Kagami, M., and Nilsson, R.H. (2018). Introducing ribosomal tandem repeat barcoding for fungi. Mol. Ecol. Res. 19: 118–127. Xu, W., Pang, K.L., and Luo, Z.H. (2014). High fungal diversity and abundance recovered in the deep-sea sediments of the Pacific Ocean. Microb. Ecol. 68: 688–698. Xu, W., Luo, Z.H., Guo, S.S., and Pang, K.L. (2016). Fungal community analysis in the deep-sea sediments of the Pacific Ocean assessed by comparison of ITS,18S and 28S ribosomal DNA regions. Deep Sea Res. Part I 109: 51–60. Xu, W., Guo, S.S., Pang, K.L., and Luo, Z.H. (2017). Fungi associated with chimney and sulfide samples from a South Mid-Atlantic Ridge hydrothermal site: distribution, diversity and abundance. Deep Sea Res. Part I 123: 48–55. Xu, W., Gong, L.F., Pang, K.L., and Luo, Z.H. (2018). Fungal diversity in deepsea sediments of a hydrothermal vent system in the Southwest Indian Ridge. Deep Sea Res. Part I 131: 16–26. Xu, W., Gao, Y.H., Gong, L.F., Li, M., Pang, K.L., and Luo, Z.H. (2019). Fungal diversity in the deep-sea hadal sediments of the Yap Trench by cultivation and high throughput sequencing methods based on ITS rRNA gene. Deep Sea Res. Part I 145: 125–136. Yang, Y., Banos, S., Gerdts, G., Wichels, A., and Reich, M. (2021). Mycoplankton biome structure and assemblage processes differ significantly along a transect from the shallow freshwater area of the Elbe River down to the river plume and the adjacent marine waters. Front. Microbiol. 12: 640469. Yang, Z.D., Jin, J., Li, B.D., Li, B.H., Li, G.F., and Diao, L.G. (2009a). Woodmarine fungi from the coast of Shandong, China Ⅵ. Mycosystema 28: 171–174. Yang, Z.D., Jin, J., Li, B.D., Luo, L., Li, G.F., and Wang, Y.L. (2009b). Woodmarine fungi from the coast of Shandong, China V. Pleospora. Mycosystema 28: 49–55. Yanna, Ho, W.H., Hyde, K.D., and Hodgkiss, J. (2001). Fungal communities on submerged wood from streams in Brunei, Hong Kong and Malaysia. Mycol. Res. 12: 1492–1501. Yusoff, M., Moss, S.T., and Jones, E.B.G. (1994a). Ascospore ultrastructure of Pleospora gaudefroyi Patouillard (Pleosporaceae, Loculoascomycetes, ascomycotina). Can. J. Bot. 72: 1–6. Yusoff, M., Read, S.J., Jones, E.B.G., and Moss, S.T. (1994b). Ultrastructure of Antennospora salina comb. nov. Mycol. Res. 98: 997–1004. Yusoff, M., Jones, E.B.G., and Moss, S.T. (1994c). A taxonomic reappraisal of the genus Ceriosporopsis based on ultrastructure. Can. J. Bot. 72: 1550–1559. Yusoff, M., Jones, E.B.G., and Moss, S.T. (1995). Ascospore ultrastructure in the marine genera Lulworthia Sutherland and Lindra Wilson. Cryptogam. Bot. 5: 307–315. Zainuddin, N., Sharuddin, S.S., and Alias, S.A. (2008). Occurrence of marine fungi from the Straits of Malacca, Malaysia, with first record of Mauritiana rhizophorae. Malay. J. Sci. 27: 61–69. 269 Zainuddin, N., Alias, S.A., Lee, C.W., Ebel, R., Mukhtar, M.R., and Awang, K. (2010). Antimicrobial activities of marine fungi from Malaysia. Bot. Mar. 53: 507–513. Zhang, S.N., Hyde, K.D., Jones, E.B.G., Jeewon, R., Cheewangkoon, R., and Liu, J.K. (2019). Striatiguttulaceae, a new pleosporalean family to accommodate Longicorpus and Striatiguttula gen. nov. from palms. MycoKeys 49: 99–129. Zhang, Z.F., Pan, Y.P., Liu, Y., and Li, M. (2021). High-level diversity of basal fungal lineages and the control of fungal community assembly by stochastic processes in mangrove sediments. Appl. Environ. Microbiol. 87: e0092821. Zhou, X., Fang, P., Tang, J., Wu, Z., Li, X., Li, S., Wang, Y., Liu, G., He, Z., Gou, D., et al. (2016). A novel cyclic dipeptide from deep marine-derived fungus Aspergillus sp. SCSIOW2. Nat. Prod. Res. 30: 52–57. Zuccaro, A., Schoch, C.L., Spatafora, J.W., Kohlmeyer, J., Draeger, S., and Mitchell, J.I. (2008). Detection and identification of fungi intimately associated with the brown seaweed Fucus serratus. Appl. Environ. Microbiol. 74: 931–941. Bionotes Ka-Lai Pang Institute of Marine Biology and Centre of Excellence for the Oceans, National Taiwan Ocean University, 2 Pei-Ning Road, Keelung 202301, Taiwan klpang@ntou.edu.tw Ka-Lai Pang obtained his BSc and PhD degrees from the City University of Hong Kong in 1998 and 2001, respectively. Prof. Pang studies the biology of marine fungi and fungus-like organisms and endophytic fungi associated with mangrove plants and macroalgae. E. B. Gareth Jones Department of Botany and Microbiology, College of Science, King Saud University, P.O Box 2455, Riyadh 11451, Kingdom of Saudi Arabia torperadgj@gmail.com https://orcid.org/0000-0002-7286-5471 Professor E. B. Gareth Jones currently holds the Distinguished Scientist Fellowship (DSFP), at the King Saud University, Kingdom of Saudi Arabia and is a highly cited scientist. His research interests are marine mycology, ecology and fungal systematics, and marine archaeology. Supervised over 100 PhD/MSc students, he has published 650 papers and edited volumes on Marine fungi (2012) and Freshwater fungi (2014). He is a senior curator of the website www.marinefungi.org .