Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 6 von 524

Details

Autor(en) / Beteiligte
Titel
Wildland fire as an atmospheric source of viable microbial aerosols and biological ice nucleating particles
Ist Teil von
  • The ISME Journal, 2021-02, Vol.15 (2), p.461-472
Ort / Verlag
London: Nature Publishing Group UK
Erscheinungsjahr
2021
Quelle
MEDLINE
Beschreibungen/Notizen
  • The environmental sources of microbial aerosols and processes by which they are emitted into the atmosphere are not well characterized. In this study we analyzed microbial cells and biological ice nucleating particles (INPs) in smoke emitted from eight prescribed wildland fires in North Florida. When compared to air sampled prior to ignition, samples of the air–smoke mixtures contained fivefold higher concentrations of microbial cells (6.7 ± 1.3 × 10 4  cells m −3 ) and biological INPs (2.4 ± 0.91 × 10 3  INPs m −3 active at temperatures ≥ −15 °C), and these data significantly positively correlated with PM 10 . Various bacteria could be cultured from the smoke samples, and the nearest neighbors of many of the isolates are plant epi- and endophytes, suggesting vegetation was a source. Controlled laboratory combustion experiments indicated that smoke emitted from dead vegetation contained significantly higher numbers of cells, INPs, and culturable bacteria relative to the green shrubs tested. Microbial viability of smoke aerosols based on formazan production and epifluorescent microscopy revealed no significant difference in the viable fraction (~80%) when compared to samples of ambient air. From these data, we estimate each fire aerosolized an average of 7 ± 4 × 10 9 cells and 2 ± 1 × 10 8 biological INPs per m 2 burned and conclude that emissions from wildland fire are sources of viable microbial aerosols to the atmosphere.
Sprache
Englisch
Identifikatoren
ISSN: 1751-7362
eISSN: 1751-7370
DOI: 10.1038/s41396-020-00788-8
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8027831

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX