A comparative study on the airborne fungi in Athens, Greece, by viable and non-viable sampling methods

Airborne fungi were studied in the city of Athens using two complementary methods in which 136 concurrent samplings were carried out during the 12-month period from January until December 1998. A portable Burkard air sampler for agar plates was used for trapping the culturable portion of the mycobiota. Nineteen genera of fungi were identified and assessed in terms of total numbers and fluctuations in concentration (Alternaria, Arthrinium, Aspergillus, Aureobasidium, Botrytis, Chrysonilia, Cladosporium, Drechslera, Epicoccum, Fusarium, Mucor, Nigrospora, Paecilomyces, Penicillium, Rhizopus, Sclerotinia, Scopulariopsis, Trichoderma and Ulocladium), with the exception of those included in the Sphaeropsidales, the yeasts, and the non-sporulating fungi, which were counted as groups. A volumetric Burkard air sampler for glass slides was operating simultaneously for detecting the total mycobiota, including the non-culturable and the non-viable portion. Ascospores, basidiospores, spores of Myxomycetes, Ustilaginales, Uredinales and Erysiphales, teliospores of Puccinia, as well as conidia of the genera Curvularia, Helminthosporium, Periconia, Pestalotiopsis, Pithomyces, Polythrincium, Stachybotrys, Stemphylium and Torula were also recorded. Only seven of the genera were recovered by both samplers. The total numbers of fungal spores, which had a maximum concentration of 3,175 spores/m(3), as well as the spore concentrations of the genera Cladosporium (2,565 spores/m(3)) and Alternaria (280 spores/m(3)) were underestimated by the viable method (2,435 CFU/m(3) for the total, 2,169 CFU/m(3) for Cladosporium and 180 CFU/m(3) for Alternaria). The non-viable method fails to resolve the identification of the genera Penicillium and Aspergillus, which are major components of the airborne mycobiota (1,068 CFU/m(3) and 204 CFU/m(3), respectively) based on recovery by the viable method.