Using flow cytometry and light-induced fluorescence to characterize the variability and characteristics of bioaerosols in springtime in Metro Atlanta, Georgia
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Published:2020-02-14
Issue:3
Volume:20
Page:1817-1838
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ISSN:1680-7324
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Container-title:Atmospheric Chemistry and Physics
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language:en
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Short-container-title:Atmos. Chem. Phys.
Author:
Negron Arnaldo, DeLeon-Rodriguez Natasha, Waters Samantha M., Ziemba Luke D., Anderson Bruce, Bergin Michael, Konstantinidis Konstantinos T., Nenes AthanasiosORCID
Abstract
Abstract. The abundance and speciation of primary biological aerosol particles (PBAP)
is important for understanding their impacts on human health, cloud
formation, and ecosystems. Towards this, we have developed a protocol for
quantifying PBAP collected from large volumes of air with a portable
wet-walled cyclone bioaerosol sampler. A flow cytometry (FCM) protocol was
then developed to quantify and characterize the PBAP populations from the
sampler, which were confirmed against epifluorescence microscopy. The
sampling system and FCM analysis were used to study PBAP in Atlanta, GA, over
a 2-month period and showed clearly defined populations of nucleic-acid-containing particles: low nucleic acid-content particles above threshold
(LNA-AT) and high nucleic acid-content particles (HNA) likely containing
wet-ejected fungal spores and pollen. We find that the daily-average springtime
PBAP concentration (1 to 5 µm diameter) ranged between 1.4×104 and 1.1×105 m−3. The LNA-AT population
dominated PBAP during dry days (72±18 %); HNA dominated the PBAP
during humid days and following rain events, where HNA comprised up to
92 % of the PBAP number. Concurrent measurements with a Wideband
Integrated Bioaerosol Sensor (WIBS-4A) showed that fluorescent
biological aerosol particles (FBAP) and total FCM counts
are similar; HNA (from FCM) moderately correlated with ABC-type FBAP
concentrations throughout the sampling period (and for the same particle
size range, 1–5 µm diameter). However, the FCM LNA-AT population,
possibly containing bacterial cells, did not correlate with any FBAP type.
The lack of correlation of any WIBS FBAP type with the LNA-AT suggests
that airborne bacterial cells may be more difficult to unambiguously detect with
autofluorescence than currently thought. Identification of bacterial cells
even in the FCM (LNA-AT population) is challenging, given that the
fluorescence level of stained cells at times may be comparable to that seen
from abiotic particles. HNA and ABC displayed the highest concentration on a
humid and warm day after a rain event (14 April 2015), suggesting that both
populations correspond to wet-ejected fungal spores. Overall, information
from both instruments combined reveals a highly dynamic airborne bioaerosol
community over Atlanta, with a considerable presence of fungal spores during
humid days and an LNA-AT population dominating the bioaerosol community during dry
days.
Funder
National Aeronautics and Space Administration Camille and Henry Dreyfus Foundation H2020 European Research Council
Publisher
Copernicus GmbH
Subject
Atmospheric Science
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