Airborne pollen and fungal spores in Garki, Abuja (North-Central Nigeria) Dimphna Nneka Ezike, Catherine V. Nnamani, Oluwatoyin T. Ogundipe & Olushola H. Adekanmbi Aerobiologia International Journal of Aerobiology including the online journal `Physical Aerobiology' ISSN 0393-5965 Aerobiologia DOI 10.1007/s10453-016-9443-5 1 23 Your article is published under the Creative Commons Attribution license which allows users to read, copy, distribute and make derivative works, as long as the author of the original work is cited. You may selfarchive this article on your own website, an institutional repository or funder’s repository and make it publicly available immediately. 1 23 Aerobiologia DOI 10.1007/s10453-016-9443-5 ORIGINALPAPER Airborne pollen and fungal spores in Garki, Abuja (North-Central Nigeria) Dimphna Nneka Ezike . Catherine V. Nnamani . Oluwatoyin T. Ogundipe . Olushola H. Adekanmbi Received: 20 November 2015 / Accepted: 11 May 2016 Ó The Author(s) 2016. This article is published with open access at Springerlink.com Abstract The ambient atmosphere is dominated with pollen and spores, which trigger allergic reactions and diseases and impact negatively on human health. A survey of pollen and fungal spores constituents of the atmosphere of Garki, Abuja (North-Central Nigeria) was carried out for 1 year (June 1, 2011–May 31, 2012). The aim of the study was to determine the prevalence and abundance of pollen and fungal spores in the atmosphere and their relationship with meteorological parameters. Airborne samples were trapped using modified Tauber-like pollen trap, and the recipient solutions were subjected to acetolysis. Results revealed the abundance of fungal spores, pollen, fern spores, algal cysts and diatoms in decreasing order of dominance. The atmosphere was qualitatively and quantitatively dominated by pollen during the period of late rainy/harmattan season than the rainy season. Numerous fungal spores were trapped throughout the sampling periods among which Alternaria spp., Fusarium spp., Cladosporium spp. and Curvularia spp. dominated. These fungi have been implicated in allergic diseases and are dermatophytic, causing diverse skin diseases. Other pathogenic fungi D. N. Ezike (&)
C. V. Nnamani Department of Applied Biology, Faculty of Science, Ebonyi State University, Abakaliki, Ebonyi, Nigeria e-mail: dimphna.nneka@yahoo.com O. T. Ogundipe
O. H. Adekanmbi Department of Botany, Faculty of Science, University of Lagos, Akoka, Lagos, Nigeria found in the studied aeroflora were Dreschlera spp., Helminthosporium spp., Torula spp., Pithomyces spp., Tetraploa spp., Nigrospora ssp., Spadicoides spp., Puccinia spp. and Erysiphe graminis. Total pollen and fungal spores counts do not show significant correlation with meteorological parameters. Keywords Abuja
Allergy
Atmosphere
Meteorological parameters
Pollen
Fungal spores 1 Introduction Pollen and fungal spores are the most dominant aeroallergens, because of their ubiquitous and wide distribution in time and space than any other representatives of living matter (Shahali et al. 2007). Their dispersal in the atmosphere is modulated by meteorological parameters such as rainfall, humidity, temperature, wind velocity and strength. Geography and vegetation also play a crucial role in the type of pollen or spores present in the atmosphere of any region (Burge 2002; Perveen et al. 2007). The clinical significance of airborne particles is largely related to their allergenicity which is influenced by their numbers and perhaps their bulk concentrations. Allergies due to pollen are seasonal, and hypersensitive individuals living in an area with high atmospheric concentration of anemophilous plants have a higher risk of developing allergic sensitization. Atmospheric 123 Aerobiologia pollen and fungal spores are recognized to provoke allergic sensitizations such as conjunctivitis, extrinsic rhinitis and asthma. Their importance in clinical allergy has been well established for many years ago (Li and Kendrick 1995). The provocation of pollen allergies is due to allergen protein contained in the sporoderm and cytoplasm (Perveen et al. 2007). Knowledge of their prevalence is required for a rational approach to diagnosis and management of allergic diseases (Chatterjee and Hargreave 1974). Airborne fungal spores’ concentration could be used as an indicator of pathogen development and could be useful when the infection levels are initially determined by inoculum rather than the weather. In these conditions, monitoring of airborne inoculums and their relationship with meteorological data provides a valuable tool for establishing the basis for an accurate modern integrated pest management strategy (Escuredo et al. 2011). Airborne pollen have proved to be extremely relevant in the evaluation of the vegetation characteristics of a study area, understanding of the flowering periodicity and in developing a functional model for predicting pollen concentration in the atmosphere. Most aeropalynological works have been carried out in Nsukka (South-East Nigeria) (Agwu and Osibe 1992; Agwu 1997; Njokuocha 2006), in Lagos (SouthWest Nigeria) (Adeniyi et al. 2014; Adekanbi and Ogundipe 2010) in Rivers State (South-south) (Agwu and Osibe 1992). The present study was carried out in Garki, Abuja, over a period of 12 months. The objectives of the study were to ascertain (a) the atmospheric pollen and fungal spores (aeroallergens) concentration in Garki, and (b) the seasonal prevalence of airborne pollen and fungal spores and their relationship to meteorological parameters. 2 Materials and methods 2.1 Study area The study was conducted in Garki, Abuja, the Federal Capital Territory of Nigeria, located north of the confluence of the River Niger and Benue River. The Federal Capital Territory has an area of 7314.2 km2, and the actual city occupies 273.3 km2. It is bordered by Niger state to the West and North, Kaduna to the 123 North-East, Nasarawa to the East and South and Kogi to the South-West (Fig. 1). The climate is influenced by two main seasons: the rainy season which lasts from May to September and dry season from October to April. The area belongs to the tropical region with average monthly temperature fluctuating between 24.7 and 34.3 °C. The mean annual rainfall varies from 19.0 to 130.3 mm. The vegetation is a mosaic of lowland Rainforest and secondary Grassland (Ofomata 1975; White 1983). The sampled site is located at 9°00 000 N and 7°300 300 E. Grassland dominates the vegetation around the trap and is characterized by Panicum maximum, Andropogon tectorum, Imperata cylindrica, Anthephora ampulacea, Imperata cylindrica, Pennisetum purpureum and Hyparrhenia barteri. The vegetation is highly diverse and includes lowland Rainforest taxa in protected areas and derived Savanna dominated by Elaeis guineensis, Alchornea cordiforlia, Pentacletra macrophylla, Gloriosa superba, etc. The herbaceous plants were dominated by Aspilia africana and Ageratum conyzoides. 2.2 Sample collection Modified Tauber-like pollen trap was employed for the collection of the airborne pollen and spores. The trap was placed at the height of 5 ft above the ground level (Fig. 2). A solution made of glycerol (50 ml), formaldehyde (10 ml) and phenol (5 ml) was prepared and poured into the trap. The recipient solutions were collected monthly for the period of 1 year. Samples were sieved through 200-lm mesh wire gauze to filter off large organic particles. The liquid with suspended palynomorphs was centrifuged at 2500 revolution per minute for 5 min to recover the palynomorphs residues. The residues were washed three times with water and were acetolyzed according to a modified version of Erdtman (1971) procedures; acetolysis mixture which consists of concentrated sulfuric acid and acetic anhydride in the ratio of 9: 1 was prepared; 5 ml of the acetolysis mixture was poured into each sample and placed in water bath for 10 min at 100 °C. They were centrifuged, decanted and washed twice with distilled water. The recovered residues were stored in vials with two drops of glycerine. Temporary slides were prepared and examined using light Olympus CH Trinocular microscope (LM), equipped with Aerobiologia Fig. 1 Map of Abuja (North-Central Nigeria), showing the study area 650 IS Cannon Digital camera at 4009 and 1009 magnifications. Identification was based on comparison with reference collection of pollen slides, description and photomicrographs of pollen and spores using books and journals (Agwu and Akanbi 1985; Y’bert 1979). Agwu (1997) and Agwu and Osibe (1992) also used Tauber-like pollen traps similar to the trap employed in this study and also the same methodology. Pollen and fungal spores obtained were counted monthly and expressed in frequency. The data obtained were analyzed using the SPSS statistical package version 20 (SPSS Inc. Chicago, Illinois USA). Correlation coefficients were generated to examine the relationship among pollen, fungal spores frequency and meteorological data. Meteorological data were obtained from Nigerian Meteorological Centre Abuja, Nigeria. 123 Aerobiologia 5 ft Fig. 2 Modified Tauber-like pollen trap in the field 3 Results Fifty-three pollen types belonging to 36 families were identified (Table 1). Three, thirteen and 37 pollen were identified to family, generic and species levels, respectively. The atmosphere was qualitatively and quantitatively dominated with varied species of fungal spores. Eighteen fungal spore types were identified (Table 2). The annual contribution of fungal spores of 3534 (54.98 %) was found to be greater than the 2852 pollen grains (45.01 %). The months with the highest pollen abundance were October 518 (17.65 %), November 472 (16.08 %) and December 354 (12.07 %). May 96 (3.37 %) and June 94 (3.29 %) had the lowest pollen records (Fig. 3). High values of fungal spores were recorded in November, which was essentially dominated by Erysiphe graminis accounting 93 % of its annual total. February with 12 spores (0.34 %) had the lowest record of fungal spores (Fig. 2; Table 2). The major pollen contributors were Poaceae 524 (18.4), Pentaclethra macrophylla 402 (14.1), Elaeis guineensis 365(12.80), Justicia spp. 211 (7.39), Cassia spp. 160 (5.6), Alchornea cordiforlia 103 (3.61) and Luffa spp. 102 (3.57). The anemophilous pollen recorded from aeroflora of Abuja include those of Poaceae, Elaies guineensis, 123 Cyperus esculenta, Amaranthaceae/Chenopodiaceae, Terminalia sp., Casuarina equisetifolia, Cocos nucifera and Dracaena arborea. The overall percentage contribution of anemophilous pollen (71 %) was higher than recorded by entomophilous pollen (29 %). Anemophilous pollen dominated from the month of June to February, while the entomophilous were more abundant from the month of September to May. Poaceae and Elaeis guineensis were the most pollen producers taxa. Poaceae pollen showed the maximum abundance in October; Elaeis guinensis pollen delayed 1 month and peaked in November (Fig. 4). Airborne pollen grains were grouped into three categories based on their sources: trees/shrubs, herbs and grasses pollen. Trees and shrubs comprised of 51.61 %, grasses and herbs reached 32.70 and 15.68 %, respectively. Trees and shrubs pollen were the bulk contributors of the atmospheric pollen, and their dominance could be demarcated between the months of September to February. The dominant trees and shrubs pollen at the studied location were: Pentaclethra macrophylla 402 (14.10), Elaeis guineensis 365 (12.80), Justicia spp. 213 (7.47), Lannea acida 71 (2.4), Alchornea cordiforlia 103 (3.61) and Khaya senegalensis 98 (3.44) among others. As regards the fungal spores, the atmosphere was dominated by different species such as Erysiphe graminis 1235 (34.95 %), Hansfordiella spp. 3209 (9.05), Puccinia spp. 294 (8.32), Nigrospora spp. 224 (6.34), Pithomyces spp. 163 (4.61) and Curvularia spp. 153 (4.33). Most spores were more abundant from the months of June to December, and their atmospheric load declined after the month of December. The relationship between pollen counts and weather parameters was correlated (Fig. 5). The total pollen counts correlated not significantly, negatively with rainfall, relative humidity and wind but positively with temperature. Poaceae pollen concentration was positively correlated with rainfall and humidity, whereas it was negatively correlated with increasing temperature and wind. The pollen of Luffa sp. showed a positive and highly significant coefficient of correlation with wind (Table 3). There was a positive but not significant correlation between the total fungal spores count and relative humidity (Table 4). However, most dominant fungal spores with the exception of Erysiphe graminis correlated Aerobiologia Table 1 Frequency of atmospheric pollen of Garki, Abuja (North-Central Nigeria), from June 2011 to May 2012 S. no Pollen Months Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Total % 1 Acacia spp. 2 0 2 2 0 0 0 0 0 0 0 0 6 0.21 2 Adansonia digitata 0 0 0 0 0 12 4 0 0 0 0 0 16 0.56 3 Ageratum conyzoides 0 0 0 0 12 0 0 16 0 0 0 0 28 0.98 4 Albizia spp. 0 2 0 0 0 0 0 0 0 0 0 0 2 0.07 5 Alchornea cordiforlia 1 0 0 12 2 52 8 2 16 4 6 0 103 3.61 6 Aloe bateri 0 0 0 0 3 0 0 0 0 0 0 0 3 0.11 7 Amaranthaceae/ Chenopodiaceae 0 0 44 8 0 16 0 4 0 0 0 0 72 2.52 8 Aneilema beninlense 0 2 0 0 0 0 0 0 0 0 0 0 2 0.07 9 Anthocleista djalonensis 0 0 0 4 0 0 0 20 0 0 0 0 24 0.84 10 Aspilia africana 0 0 6 22 2 8 0 0 0 0 1 6 45 1.58 11 12 Asteraceae Bridelia ferruginea 4 0 0 0 0 0 0 0 0 24 0 0 0 0 0 0 0 0 0 0 0 0 0 0 4 24 0.14 0.8 13 Bulbostylis filamentosa 0.14 14 Cassia spp. 15 0 0 0 0 0 0 4 0 0 0 0 0 4 28 0 0 4 10 8 0 0 8 30 16 56 160 5.6 Casuarina equisetifolia 1 6 2 0 0 0 0 0 0 8 6 4 27 0.95 16 Ceiba pentandra 0 4 0 0 0 0 0 0 0 0 0 0 4 0.14 17 Celtis zenkeri 0 0 0 0 0 16 20 0 0 0 0 0 36 1.26 18 Cissus spp. 0 0 0 2 0 0 0 0 0 0 0 0 2 0.1 19 Cochlospermum tinctorum 0 16 0 0 0 0 42 0 0 0 0 0 58 2.03 20 Cocos nucifera 4 0 0 0 0 0 0 0 0 0 0 0 4 0.14 21 Crotalaria spp. 0 0 0 0 0 0 0 6 4 0 0 0 10 0.35 22 Cyperus esculenta 0 0 0 4 0 44 4 1 10 6 2 2 73 2.56 23 Dichrostachys cinera 0 0 0 0 0 0 2 8 0 0 0 10 0.35 24 Dracaena arborea 0 0 8 0 2 0 0 0 0 0 0 0 10 0.35 25 Drypetes gilgiana 0 0 0 0 0 0 2 0 0 0 0 0 2 0.07 26 27 Eichlornia natans Elaeis guineensis 2 118 0 6 0 8 0 5 0 0 6 206 0 8 0 8 0 8 0 0 0 0 0 0 2 365 0.07 12.80 28 Eugenia spp. 0 0 0 0 2 0 0 0 0 0 0 0 2 0.07 29 Gardenia imperialis 0 0 0 0 0 0 2 0 0 0 0 0 2 0.07 30 Gloriosa superba 0 0 2 0 32 0 2 6 0 0 0 0 42 1.50 31 Hexabolus scrispiflorus 0 0 0 0 0 0 8 0 0 0 0 0 8 0.28 32 Hymenocardia acida 0 2 4 12 12 0 0 0 6 0 20 0 56 1.96 33 Ipomea spp. 0 0 0 0 0 0 0 8 32 0 0 0 48 1.68 34 Justicia spp. 0 8 8 0 0 2 4 13 18 134 14 12 213 7.47 35 Khaya senegalensis 3.44 36 Lannea acida 37 0 0 2 30 18 48 0 0 0 0 0 0 98 63 6 2 0 0 0 0 0 0 0 0 0 71 2.40 Lannea welwitschii 0 0 2 0 0 0 0 0 0 0 0 0 2 0.07 38 Lophira alata 0 0 0 0 2 0 0 0 0 0 0 0 2 0.07 39 Luffa spp. 0 0 0 0 21 2 0 6 12 26 73 2 102 3.58 40 Marantochloa cuspidate 0 0 2 0 0 0 0 0 0 0 0 0 2 0.07 41 42 Milletia spp. Olax subscorpoides 2 0 0 0 0 0 0 0 0 0 0 0 0 12 0 12 0 0 0 0 0 0 0 0 2 24 0.07 0.84 43 Parkia biglobosa 2 0 0 0 6 0 0 16 0 0 0 0 24 0.84 123 Aerobiologia Table 1 continued S. no Pollen Months Jun 44 Pentaclethra macrophylla 45 Poaceae 46 Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Total % 0 0 4 120 0 36 188 54 0 0 0 0 402 14.10 48 44 44 68 248 20 28 16 8 0 0 0 524 18.37 Phyllanthus discoides 2 0 0 0 0 0 0 0 0 0 0 0 2 0.07 47 Polygala multiflora 0 0 2 0 0 0 2 0 0 0 0 0 4 0.14 48 Solenostemon monostachys 0 0 0 0 0 0 0 2 0 0 0 0 2 0.07 0.50 49 Syzygium spp. 50 Uapaca togoensis 51 Terminalia spp. 0 0 0 0 0 0 12 2 0 0 0 0 14 14 0 0 0 4 0 0 0 2 2 8 14 44 1.54 4 0 0 0 0 0 2 0 0 0 0 0 6 0.21 52 Vernonia spp. 0 0 0 0 0 0 0 12 0 0 0 0 12 0.42 53 Vigna multinervis 0 0 0 0 0 2 0 0 0 0 0 0 2 0.07 294 94 142 181 518 472 354 212 124 210 146 96 2852 Total pollen Table 2 Frequency of atmospheric fungal spores of Garki, Abuja (North-Central Nigeria), from June 2011 to May 2012 S. no Fungal spores Months Jun 1 Alternaria spp. 2 3 Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Total % 14 4 0 6 0 0 0 0 0 0 18 28 70 1.98 Apiosporina spp. 0 0 0 0 2 0 0 0 0 0 0 0 2 0.06 Aspergillus spp. 0 0 2 0 0 0 1 0 0 0 0 0 3 0.08 4 Cercosporella spp. 3 0 0 0 0 0 0 0 0 0 0 0 3 0.08 5 Cladosporium spp. 15 24 0 0 45 0 8 4 0 0 0 0 96 2.72 6 Curvularia spp. 0 4 12 9 96 2 0 18 12 0 0 0 153 4.33 7 Erysiphe graminis 0 0 2 0 0 1200 24 9 0 0 0 0 1235 34.95 8 Fusarium spp. 0 0 6 0 0 20 0 0 0 0 0 0 26 0.74 9 Hansfordiella spp. 37 123 90 6 64 0 0 0 0 0 0 0 320 9.05 10 Helminthosporium sp. 6 0 6 30 0 6 8 0 0 0 0 0 56 1.58 11 Pithomyces spp. 12 15 20 20 54 6 36 0 0 0 0 0 163 4.61 12 Nigrospora spp. 51 6 48 12 45 12 0 6 0 24 10 10 224 6.34 13 Puccinia spp. 12 28 189 60 3 1 1 0 0 0 0 0 294 8.32 14 Spadicoides spp. 0 75 0 30 46 0 0 0 0 20 0 0 171 4.84 15 16 Sporidesmium spp. Tetraploa spp. 32 111 0 3 0 9 0 3 165 2 0 0 0 12 0 0 0 0 0 0 0 0 0 0 197 140 5.57 3.96 17 Torula spp. 15 28 6 12 3 1 1 0 0 0 0 0 66 1.87 18 Venturia spp. 0 0 0 1 8 0 0 0 0 0 0 0 9 0.25 19 Indeterminate 2 2 120 21 40 24 84 0 0 0 0 0 293 8.29 310 312 510 210 573 1285 175 37 12 44 28 38 3534 Total pollen positively with rainfall and relative humidity and negatively with the wind (Table 4). Puccinia spp. showed a negative and highly significant coefficient of correlation with temperature. Hansfordiella spp. 123 was associated positively and significantly with relative humidity (Table 4). The photomicrographs of some recovered pollen and fungal spores are shown in Fig. 6. Aerobiologia Absolute pollen and spores counts 1400 1200 1000 800 POLLEN 600 SPORES 400 200 0 JUN JLY AUG SEP OCT NOV DEC JAN FEB MCH APL MAY 300 Elaeis Poaceae 250 200 150 100 50 0 JUN JLY AUG SEP OCT NOV DEC JAN FEB MCH APL MAY Months Fig. 4 Monthly variations of Poaceae and Elaeis guineensis pollen from June 2011 to May 2012 in Garki 4 Discussion The results provided detailed information about the relative abundance of the source plants as well as their pollination periods. The number of pollen types (53) recorded in this work for 1 year is higher compared to 40 pollen types belonging to twenty-six families recovered in 1 year in two sampling sites in Nsukka plateau, South-East Nigeria (Njokuocha 2006). Thirty-seven pollen types belong to 30 families in Shomolu Local Government Area, South-West Nigeria (Adeniyi et al. 2014). The vegetation was therefore inferred rich and more diverse than previous studied areas in Nigeria. Flowering was observed throughout the year though with some variations. The dominant trees, shrubs and grass pollen at the studied location Mean monthly temperature, rainfall, relaƟve humidity and wind Values of Elaeis guinensis and Poaceae Fig. 3 Monthly variations of atmospheric pollen and fungal spores from June 2011 to May 2012 in Garki 300 T R 250 R.H 200 W 150 100 50 0 Months Fig. 5 Mean monthly values of meteorological parameters in Garki (June 2011–May 2012). Mean monthly values of meteorological parameters in Garki (June 2011–May 2012). T Mean monthly temperature (°C), R mean monthly rainfall (mm); R.H. mean monthly relative humidity (%), W, mean monthly wind speed (km/h) reflect the mosaic of lowland Rainforest and secondary Grassland ecotype as indicated by Ofomata (1975) and White (1983). This is consistent with the work of Nnamani and Uguru (2013), who reported the abundance of these species in their work carried out in Nigeria. The atmosphere contained more pollen during the dry season (October to March), especially at harmattan period (October to January) than the rainy season (April to September). Major pollen contributors during the rainy season were Poaceae and Elaeis guineensis, and they reached their monthly maximum load in dry season. Large recovery of Elaeis 123 Aerobiologia Table 3 Correlation coefficients between frequency of pollen and meteorological parameters Pollen count R R.H W Alchornea cordiforlia -.466 .111 -225 -.106 Cyperus spp. Elaeis guineensis -.434 .109 -.293 -.237 .004 .044 Justicia spp. T .334 -.213 .346 -.273 -.293 Luffa spp. -.186 .347 -.132 Pentaclethra macrophylla -.371 -.016 -.443 -.120 .289 -.162 .415 -.411 -.352 .019 -.176 -.243 Poaceae Total pollen count .334 .917** ** Correlation is significant at p = 0.01 level (2-tailed) R mean monthly rainfall (mm), T mean monthly temperature (°C), R.H mean monthly relative humidity (%), W mean monthly wind speed (km/h) Table 4 Correlation coefficients between frequency of fungal spores and meteorological parameters Spores count Curvularia spp. R T R.H W .087 -.087 .211 -.323 Erysiphe graminis -.312 .022 -.097 -.146 Hansfordiella spp. .555 -.558 .654* Nigrospora spp. .279 -.507 .590 -.291 Pithomyces spp. .236 -.317 .262 -.400 Puccinia spp. .485 -.933** .497 -.298 Spadicoides spp. .550 .067 .499 -.246 Sporidesmium spp. .100 .010 .299 -.286 Tridentarium spp. .094 -.058 .249 -.133 -.021 -.324 .266 -.405 Total fungal spores -.373 ** Correlation is significant at the p = 0.01 level (2-tailed) * Correlation is significant at the p = 0.05 level (2-tailed) R mean monthly rainfall (mm), T mean monthly temperature (°C), R.H. mean monthly relative humidity (%), W mean monthly wind speed (km/h) guineensis pollen could reflect the extent of palm forest within the study area. More pollen dominated the atmosphere at dry and more windy periods than the rainy and humid periods. Harmattan period (October to January) was designated as a higher risk period for hypersensitive individuals to pollen. The greater intensity of rainfall inferred through its amount and duration leads to a decline in pollen morphotypes, since rainfall washes down suspended pollen in the atmosphere. 123 Among the anemophilous pollen, Poaceae and Elaeis guinensis pollen were the most abundant. Njokuocha (2006) and Agwu and Osibe (1992) also found them preponderant in their studies. Poaceae pollen include the wild and cultivated grass pollen, which were more abundant from June and December; pollen allergies at this period could be attributed partly to their higher antigenic load. Taketomi et al. (2008) founded the pollen of Poaceae family as a major sensitizing agent in patients with pollinosis. D’Amato et al. (2007) stated also that grass-induced pollinosis is the most common pollen allergy in Europe. Anemophilous pollen have been reported to be more implicated in allergies because of their higher atmospheric load. Chatterjee and Hargreave (1974) stated that they also have better aerodynamic properties than the entomophilous pollen. Furthermore, anemophilous plants produce more pollen than entomophilous species as their pollination is hazardous. This could have led to their more preponderance than the latter. Their smaller sizes make them easily trapped on skin, conjunctiva of the eyes and mucous membrane of the nose; they might penetrate the lower respiratory tract and induce symptoms of bronchial asthma and/or hay fever (Abou Chakra et al. 2009). The dominance of Erysiphe graminis coincided with the decline of Poaceae pollen as Erysiphe graminis is a pathogenic fungi on species of Poaceae. The decline of pollen at the months of lower rainfall could also be due to post-anthesis and the persistence annual bush fires which usually occur during the harmattan period in South-East and North-Central Nigeria. Total pollen counts correlated negatively with rainfall, relative humidity and wind but positively with temperature. These findings are similar to those of Barnes et al. (2000), Teranishi et al. (2000), Riberio et al. (2003) and Njokuocha (2006), who found that airborne pollen concentration correlated significantly and positively with temperature and is correlated negatively with rainfall and number of rainy days. In contrast to our results, several studies obtained significant and positive correlations between daily Poaceae pollen concentration and daily maximum temperature (Valencia-Barrera et al. 2001; Green et al. 2004) or daily minimum temperature (Green et al. 2004). In this study, pollen was dominated in the month of October followed by November, and the fungal spores dominated in the month of November followed by October. This is contrary to Essien and Aerobiologia 25 μm 4 μm 38 μm F E D 33 μm C B A 8 μm 15 μm G 1 μm Fig. 6 Photomicrographs of some recovered pollen and fungal spores in the atmosphere of Garki. Pollen a Elaeis guineensis, b Bombax buonopozense, fungal spores c Curvularia sp.; d Tridentarium sp.; e Alternaria sp.; f Nigrospora sp.; g, Fusarium sp. All magnifications 9400 Oluwagbemiga (2014), who found pollen more abundant in the month of May followed by June and spores more preponderant in the month of December followed by March, in the atmosphere of Anyigba, Kogi State, Nigeria. The study also was contrary to Njokuocha (2006), who found pollen more abundant in September followed by December in the atmosphere of Nsukka, Nigeria. The highly significant positive correlation of Luffa sp. to wind unlike the other dominant pollen indicates its pollen transport is being influenced by the prevailed local wind in the month of April and probably its localization on the trajectory of the dominant wind direction. Alternaria spores were only present during the rainy season from April to September. Escuredo et al. (2011) also reported their presence in the atmosphere 123 Aerobiologia and their impacts on agricultural crops and human health risks. Alternaria spores are potential source of allergic disorders in human beings (Escuredo et al. 2011). Alternaria solani produces an early blight in potato crops. The pathogen can infect all aerial parts of Solanaceous crops including tomato, potato, eggplant and pepper, as well as potato tubers (Tsitsigiannis et al. 2008). Only a significant positive correlation was observed with W (Luffa sp.), RH (Hansfordiella spp.) and significant negative correlation with T (Puccinia spp.). The positive correlation of 80 % of dominant fungal spores with rainfall and 90 % with relative humidity is probably related to the sporulation of fungi during the rainy season. This agrees with Lyon et al. (1984), who found significant correlation between humidity and ascospores. This finding also agrees with the report by Phanichyakarn et al. (1989), who also found dominance of fungal spores in the rainy season and lower in the dry season in the atmosphere of Bangkok. Sabariego et al. (2000) found different indices in the correlation coefficients between fungal spores concentration and meteorological parameter. From the result, 3 pollen dispersal patterns and 1 fungal season were detected: 1. 2. 3. 4. Pollen morphotypes recorded in dry season and dominated by pollen from Elaeis guineensis, Poaceae, Cassia spp., Justicia spp., Luffa spp. and Pentaclethra macrophylla Pollen morphotypes recorded during rainy season with long season (Elaeis guineensis, Poaceae) and short season (Lannea acida, Cassia spp.) Pollen morphotypes recorded during harmattan period dominated by Poaceae, Elaeis guineensis, Khaya senegalensis, Cyperus spp., Alchornea cordiforlia, Pentaclethra macrophylla. Rainy to late rainy season dominated by most fungal spores. 5 Conclusion This study contributes to the knowledge of the pollen and spore content of the atmosphere of Garki, Abuja. Their presence in the air was influenced by weather parameters, geography and vegetation. As a result of these variables, their atmospheric count vary from one season to the other, resulting in a more pollen load during the dry season, especially during the harmattan 123 period and more fungal spores load during the rainy season with the exception of Erysiphe graminis in November. The occurrence of some dominant fungal spores could be an indicator of pathogen development in the area and could warn the farmers and agriculturists to protect their crops from diseases. We consider it necessary to include more years of sampling in order to establish correlation between total pollen and fungal spores counted and meteorological parameters. Acknowledgments We sincerely appreciate the Department of Botany, University of Lagos, Akoka, for the provision of laboratory equipment for this research. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:// creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. References Abou Chakra, O. R., Lacroix, G., Peltre, G., Rogerieux, F., Sénéchal, H., & Sutra, J. P. (2009). Immunological interactive effects between Pollen grains and their cytoplasmic granules on brown Norway Rats. Word Allergy Organization Journal, 2, 201–207. Adekanbi, O., & Ogundipe, O. T. (2010). Aeropalynological studies of the University studies of the University of Lagos Campus, Nigeria. Notulae Scientia Biologicae, 2(4), 34–39. Adeniyi, T. A., Adeonipekun, P. A., Olowokudejo, J. P., & Akande, I. S. (2014). Airborne Pollen records of Shomolu local government area in Lagos state. Notulae Scientia Biologicae, 6(4), 428–432. Agwu, C. O. C. (1997). Modern pollen rain in Nsukka: An indicator of the vegetation of Nsukka Plateau. Wurzburger Geographie Arbied, 92, 97–115. Agwu, C. O. C., & Akanbi, T. O. (1985). A palynological study of honey from four vegetation zones of Nigeria. Pollen et Spores, 27, 335–348. Agwu, C. O. C., & Osibe, E. E. (1992). Airborne palynomorphs of Nsukka during the months of February–April 1990. Nigerian Journal of Botany, 5, 177–185. Barnes, C., Pachecco, F., Landuyt, J., Frank, H., & Portnoy, J. (2000). The effect of temperature, relative humidity and rainfall on airborne ragweed pollen concentrations. Aerobiologia, 17, 61–68. Burge, H. A. (2002). An update on Pollen and fungal spore aerobiology. Journal of Allergy and Clinical Immunology, 110, 544–552. Chatterjee, J., & Hargreave, F. E. (1974). Atmospheric pollen and spores in Hamilton in 1972 estimated by the Hirst automatic volumetric spore trap. Canadian Medical Association Journal, 110, 659–663. Aerobiologia D’Amato, G. D., Cecchi, L., Bonini, S., Nunes, C., AnnesiMaesano, I., Behrendt, H., et al. (2007). Allergenic pollen and pollen allergy in Europe. Allergy, 1111, 1398–1413. Erdtman, G. (1971). An introduction to Pollen analysis. Waltham, MA: Chronica Botanica. Escuredo, O., Fernández-González, M., Iglesias, I., & Seijo, M. C. (2011). Effects of meteorological factors on the levels of Alternaria spores on a potato crop. International Journal of Biometerology, 10, 234–239. Essien, B. C., & Oluwagbemiga, A. D. (2014). The role of airborne pollen grains of some Angiosperms and fungal spores in allergic and pathogenic infection in Anyigba, Kogi State, Nigeria. International Journal of Advances in Medical Sciences and Biotechnology, 2(3), 23–28. Green, B. J., Dettmann, M., Yli-Panula, E., Rutherford, S., & Simpson, R. (2004). Atmospheric Poaceae pollen frequencies and associations with meteorological parameters in Brisbane, Australia: a 5-year record, 1994–1999. International Journal of Biometeorology, 48, 172–178. Li, D. W., & Kendrick, B. (1995). A year round comparison of fungal spores in indoor and outdoor air. Mycologia, 87(2), 190–195. Lyon, F. L., Kramer, C. L., & Eversmeyer, M. G. (1984). Variation of airspora in the atmosphere due to weather conditions. Grana, 23, 177–181. Njokuocha, R. C. (2006). Airborne pollen grains in Nsukka, Nigeria. Grana, 45, 73–80. Nnamani, C. V., & Uguru, A. N. (2013). Diversity of honey producing plants of southern Nigeria: basic requisite for conservation and sustainability. Journal of Sustainable Science and Management, 8(1), 103–112. Ofomata, G. E. (1975). Nigeria in maps. Benin City: East St, Athiope Publ. H. Perveen, A., Qaiser, M., & Sad-ul-Islam, M. (2007). Airborne pollen survey of Karachi and adjacent areas in relation to allergy. World Applied Sciences Journal, 2(4), 289–298. Phanichyakarn, P., Kraisarin, C., & Sasisakulporn, C. (1989). Atmospheric pollen and mold spores in Bangkok: A 15 year survey. Asian Pacific Journal of Allergy and Immunology, 7, 113–118. Riberio, H., Cunha, M., & Abreu, I. (2003). Airborne pollen concentration in the region of Braga, Portugal and its relationship with meteorological parameter. Aerobiologia, 19, 21–27. Sabariego, S., Diaz, G. C., & Alba, F. (2000). The effect of meteorological factors on daily variation of airborne fungal spores in Granada (southern Spain). International Journal of Biometeorology, 44(1), 1–5. Shahali, Y., Majd, A., Pourpak, Z., Tajadod, G., Haftlang, M., & Mostafa, M. (2007). Comparative study of the pollen protein contents in two major varieties of Cupressus arizonica planted in Tehran. Iranian Journal of Allergy, Asthma and Immunology, 6(3), 123–127. Taketomi, E. A., Sopelete, M. C., Vierra, P. F., & Moreira, F. M. C. (2008). Pollen allergic disease: Pollen and its major allergens. Revista Brasileira otorrinolaringologia. doi:10. 1590/50034-7299200640004000. Teranishi, H., Kenda, Y., Katoli, T., Kasuya, M., Oura, E., & Taira, H. (2000). Possible role of climate change in the pollen scatter of Japanese cedar, Crptomeria japonica. Aerobiology, 14, 65–70. Tsitsigiannis, D. I., Antoniou, P. P., & Tjamos, S. E. (2008). Major diseases of tomato, pepper and egg plant in green houses. The European Journal of Plant Science and Biotechnology, 2, 106–124. Valencia-Barrera, R. M., Comtois, P., & Fernández-González, D. (2001). Biogeography and bioclimatology in pollen forecasting—An example of grass in León (Spain) and Montreal (Canada). Grana, 40, 223–229. White, F. (1983). The vegetation of Africa. IAPT, 33, 549–555. Y’bert, J. P. (1979). Atlas des pollen de cote d’Ivoire. Paris: Orstom. 123