Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/146
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dc.contributor.authorBreka, Katarinaen_US
dc.contributor.authorStupar, Milošen_US
dc.contributor.authorVidaković, Danijelaen_US
dc.date.accessioned2019-06-20T20:11:34Z-
dc.date.available2019-06-20T20:11:34Z-
dc.date.issued2018-09-
dc.identifier.citationExplore and protect the natural beauty of Balkans. International Rufford Small Grants Conference. 27th – 28th September, 2018, Silver Lake, Serbia. Abstract Booken_US
dc.identifier.isbn978-­86-­912033-­2-­0-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/146-
dc.description.abstractRecent research of frog skin microbiota were mainly focused on presence of pathogens, especially Batrachochytrium dendrobatidis, as well as on describing the bacterial communities on their skin. The specialized amphibian lifestyle where frogs’ skin is in intimate contact with the environment is of primary importance in determining frogs’ resilience to external factors. Cutaneous microbiota is thus an indicator of both frog health as well as of environmental factors acting upon frogs. Many of these factors can be detrimental to frog fitness and it is expected that the first changes in frog fitness could be assessed by identifying the changes in diversity patterns of frog’s skin epibiotic communities and/or isolating specific pathogens. Knowledge of these communities and patterns could contribute to more efficient conservation. Epibiotic communities of the green frog complex (Pelophylax esculenta complex), sampled on three localities in South Banat, Serbia (Stevanove Ravnice, Jaruga canal, Danube­-Tisa-­Danube Canal) were investigated using culture depended methods and microscopy techniques. Samples were collected using three sampling methods: 1) scraping by toothbrush for algal sample 2) swabbing with sterile cotton swabs for fungal sample and 3) nonaggressive adhesive tape method for both algal and fungal sample. The aim of this research was describing fungal and algal communities present on frogs’ skin. Culture based methods showed high diversity of air-­ and soil­-borne fungi (members of genera Acremonium, Alternaria, Aspergillus, Bionectria, Bipolaris, Botrytis, Cladosporim, Epicoccum, Fusarium, Penicillium, Trichoderma, Ulocladium, to name a few), which could be considered transients. However, microscopy techniques revealed spore germination, mycelia formation and sporulation directly on frog skin, of some typical soil­borne fungi eg. Fonseceae sp., causative agent of amphibian chromomycoses as well as human phaeohyphomycosis. Microscopy analyses of samples taken or scraped from amphibians’ skin showed the presence of morphological structures belonging to aeroaquatic hyphomycetes (eg. Canalisporium sp.) and stramenopiles, as well as high abundance of diatoms. Presence of c. 40 diatom genera was observed with dominance of mostly ubiquitous eurivalent species found in highly eutrophic waters (members of genera Amphora, Craticula, Cymbella, Cymbopleura, Cymatopleura, Diploneis, Encyonema, Epithemia, Fallacia, Gomphonema, Luticola, Navicula, Neidium, Nitzschia, Pinnularia, Planothidium, Rhopalodia, Staurosira and Surirella).en_US
dc.language.isoenen_US
dc.publisherAssociation for sustainable development and habitat protection “HabiProt”en_US
dc.relationRufford project No. 19434-1en_US
dc.titleHidden dwellers on green frog’s skin (Pelophylax esculenta complex)en_US
dc.typeConference Paperen_US
dc.relation.conferenceExplore and protect the natural beauty of Balkans. International Rufford Small Grants Conferenceen_US
dc.date.updated2023-10-14-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeConference Paper-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Animal Ecology and Zoogeography-
crisitem.author.deptChair of Algology, Mycology and Lichenology-
crisitem.author.orcid0000-0001-8775-8057-
crisitem.author.orcid0000-0002-9258-5688-
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