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Outdoor airborne fungi captured by viable and non-viable methods
Institution:1. Department of Botany, Lublin University of Life Sciences, Akademicka 13, 20-950 Lublin, Poland;2. Department of Environmental Biology, University of Rzeszow, Zelwerowicza 4, 35-601 Rzeszow, Poland;3. Laboratory of Aeropalynology, Faculty of Biology, Adam Mickiewicz University, Poznan, Poland;4. Department and Clinic of Dermatology, University of Medical Sciences, Przybyszewskiego 49, 60-355 Poznan, Poland;5. Institute of Plant Genetics, Polish Academy of Sciences, Strzeszynska 34, 60-479 Poznan, Poland;6. Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704 Poznan, Poland;7. Department of Crystallography, Faculty of Chemistry, Adam Mickiewicz University, Umultowska 89b, 61-614 Poznan, Poland
Abstract:Volume assessments of the concentration of airborne fungi may provide different results depending on the methodology used. This work simultaneously analyses two methods for samples obtained outdoors and analysed in the context of meteorological conditions. The study was carried out in Badajoz (SW Spain) from Mar. 2009 to Jul. 2011. A Burkard fixed spore trap was used for the non-viable sampling, and three different methods were used for the viable sampling: a Burkard portable spore trap with two inlet port types and a Sampl'air AES trap. Daily average total concentrations of 285 CFU m−3 and 1 954 spores m−3 were recorded for the viable and non-viable methods, respectively. The spore/colony ratio showed important differences among the most relevant fungal types: Alternaria (2.6), Aspergillus–Penicillium (2.0) and Cladosporium (11.1). Although the two sampling types were essentially equivalent at showing temporal variations in outdoor airborne fungi, quantitative differences in the number of total colonies recorded depended on the culture media and conditions used.
Keywords:Aeromycology  Outdoor airborne fungi  Viable and non-viable sampling methods
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