Cycling and effects of primary biological aerosol particles in the atmosphere and biosphere (adapted from Pöschl, 2005).
Table 1. Characteristic types of primary biological aerosol particles (PBAP)
Particle types
Examples
Biological organisms or dispersal units (dead or alive, isolated or aggregated)
Bacteria, fungi, protozoa, algae, spores, pollen, lichen, archaea, viruses, etc.
Solid fragments or excretions of biological organisms or dispersal units
Detritus, microbial fragments, plant debris/leaf litter, animal tissue and excrements, brochosomes, etc.
Table 2. Taxonomic information on biological particles in air mentioned in the review
Column density of bacterial tracer (106 m−2), simulated from estimated emissions for a set of ten ecosystems estimates (Burrows et al., 2009b).
Fig. 3.
Fungal spores with and without coating by secondary organic aerosol (dark gray envelope in left panel). Electron micrographs of aerosol filter samples from pristine tropical rainforest air in the Amazon (Pöschl et al., 2010), (Reproduced with permission from AAAS).
Table 3. Global emission estimates for different types of PBAP and size ranges of air particulate matter (PMx, x = upper limit of particle diameter; TSP = total suspended particulates)
Global emissions (Tg yr−1)
Size range
References
Bacteria
0.74 (0.4–1.8)
Diameter: 1 µm (PM1)
Burrows et al. (2009b)
0.7
Diameter: 1 µm (PM1)
Hoose et al. (2010a)
2.58
Diameter: 1.17 µm
A. Sesartic, personal communication
28.1
Lognormally distributed with geometric mean number diameter: 2 µm, standard deviation = 1.37
Jacobson and Streets (2009)
Fungal spores
8
Diameter: 4 µm (PM4)
Sesartic and Dallafior (2011)
28
Two size modes: fine (<2.5 µm) and coarse (2.5–10 µm) (PM10)
Heald and Spracklen, (2009)
31
Diameter: 5 µm (PM5)
Hoose et al. (2010a)
50
Diameter: 5 µm (PM5)
Elbert et al. (2007)
186
Lognormally distributed with geometric mean number diameter: 3 µm, standard deviation = 1.37
Jacobson and Streets (2009)
Pollen
47
Diameter: 30 µm (PM30)
Hoose et al. (2010a)
84
Lognormally distributed with geometric mean number diameter: 30 µm, standard deviation = 1.37
Jacobson and Streets (2009)
Total PBAP
<10 (dominated by plant debris and fungal spores),
Diameter: 4 µm for fungal spores; diameter not specified for plant debris (TSP)
Winiwarter et al. (2009)
56 (0–90)
Diameter <2.5 µm (PM2.5)
Penner (1995)
78 (includes only bacteria, fungal spores and pollen)
Diameters as above (PM30)
Hoose et al. (2010a)
186
Split equally into the two coarse size fractions: 2.5–5 and 5–10 µm (PM10)
Mahowald et al. (2008)
296 (includes only bacteria, fungal spores and pollen)
Diameters as above
Jacobson and Streets, (2009)
~1000 (includes cellular fragments)
TSP
Jaenicke (2005)
Table 4. Characteristic magnitudes of the number and mass concentrations of PBAP in air over vegetated regions
Number concentration
[m−3 air]
Mass concentration [µg m−3]
Size range
References
Bacteria
~104
~0.1
PM10
Bauer et al. (2002a); Burrows et al. (2009a)
Plant debris (free cellulose)
~0.1–1
PM10
Sánchez-Ochoa et al. (2007)
Viral particles
~104
~10−3
This work, Sect. 2.4
Fungal spores
~103–104
~0.1–1
TSP
Elbert et al. (2007); Fröhlich-Nowoisky et al. (2009)
Fungal hyphal fragments
~103
Pady and Gregory (1963)
Pollen
~10 (up to ~103)
~1
TSP
Sofiev et al. (2006); Fröhlich-Nowoisky et al. (2009)
Algae
~100 (up to ~103)
~10−3
Reisser (2002)
Fern spores
~10 (up to ~103)
~1
TSP
Mücke and Lemmen (2008)
Fig. 4.
Characteristic time series and number size distribution of fluorescent biological aerosol particles (FBAPs) measured with an ultraviolet aerodynamic particle sizer (UV-APS) in central Europe (Mainz, Germany, October 2006). The peaks at ~1.5, ~3 and ~13 µm can be attributed to bacteria, fungal spores, and pollen. NF,c is the number concentration of FBAPs, and NT,c is the number concentration of total aerosol particles with aerodynamic diameters Da>1 µm; dNF/dlogDa is the number size distribution function of FBAPs (Huffman et al., 2010).
Table 5. Compilation of laboratory measurements of the hygroscopic properties of biological particles (n.a.=data not available)
Measurements at subsaturation
Measurements at supersaturation
Diameter, Dve–volume equivalent, Dgma. geometric mass aerodynamic, Dmma – mass median aerodynamic, Da – aerodynamic
Maximum growth factor at RH
RH at which hygroscopic growth was measured
Critical supersaturation
CCN/CN ratio
References
BacteriaPseudomonas syringae, Erwinia herbicola
n.a.
–
–
activation observed at 0.5%
n.a.
Snider et al. (1985)
Erwinia carotovora
3 µm (maximum cellular dimension)
–
–
0.2% to 2.2%
≤ 0.5
Franc and DeMott (1998)
Arthrobacter agilis
1.1 µm Dve
–
–
0.11%
1.03±0.7
Bauer et al. (2003)
“new species”
1.1 µm Dve
–
–
0.11%
0.88±0.5
Bauer et al. (2003)
Sphingomonas echinoides
1.2 µm Dve
–
–
0.09%
0.92±0.6
Bauer et al. (2003)
Sphingomonas echinoides – fixed
1.2 µm Dve
–
–
0.07%
0.99±0.4
Bauer et al. (2003)
Saccharomonospora viridis
1.15 µm Dgma
1.3 at 95%
95%
–
–
Madelin and Johnson (1992)
Streptomyces albus
1.15 µm Dgma
1.09 at 95%
95%
–
–
Madelin and Johnson (1992)
Bacillus subtilis
0.94 µm Dmma
~1.22 at 90%
10–90%
–
–
Johnson et al. (1999)
Pseudomonas syringae
0.89 µm Dmma
~1.15 at 90%
10–90%
–
–
Johnson et al. (1999)
Escherichia coli
0.63 µm Da
1.34 at 98%
20–98%
–
–
Lee et al. (2002)
Bacillus subtilis
0.75 µm Da
1.16 at 98%
20–98%
–
–
Lee et al. (2002)
Fungal sporesAspergillus flavus
3.3 µm Dgma
1.15 at 95%
95%
–
–
Madelin and Johnson (1992)
Aspergillus fumigatus
1.9 µm Dgma
1.16 at 98%
95 and 98%
–
–
Madelin and Johnson (1992)
Cladosporium cladosporioides
2.3 µm Dgma
1.12 at 98%
95 and 98%
–
–
Madelin and Johnson (1992)
Paecilomyces variotii
2.5 µm Dgma
1.06 at 98%
95 and 98%
–
–
Madelin and Johnson (1992)
Penicillium chrysogenum
2.6 µm Dgma
1.07 at 98%
95 and 98%
–
–
Madelin and Johnson (1992)
Penicillium minioluteum
1.6 µm Dgma
1.12 at 98%
95 and 98%
–
–
Madelin and Johnson (1992)
Scopulariopsis brevicaulis
5.1 µm Dgma
1.08 at 95%
95%
–
–
Madelin and Johnson (1992)
Penicillium brevicompactum
2.9 µm Dgma
~1.05 at 90%
30–100%
–
–
Reponen et al. (1996)
Penicillium melinii
2.4 µm Dgma
~1.08 at 90%
30–100%
–
–
Reponen et al. (1996)
Aspergillus versicolor
2.1 µm Dgma
~1.07 at 90%
30–100%
–
–
Reponen et al. (1996)
Aspergillus fumigatus
2.1 µm Dgma
~1.06 at 90%
30–100%
–
–
Reponen et al. (1996)
Cladosporium cladosporioides
1.8 µm Dgma
~1.04 at 90%
30–100%
–
–
Reponen et al. (1996)
Pollen
various ragweed, amaranth-chenopod and grass pollens
n.a.
Mass increase by up to a factor of 2
‘very dry’ to ‘moist’
–
–
Durham (1943)
Ambrosia artemisiifolia
20 µm
Effective density increase: 1.52 at 93–100%, no geometric growth
11–100%
–
–
Harrington and Metzger (1963)
various pollens (deciduous trees, conifers and grasses)
22 to 115 µm
Mass increase by up to a factor of 4 at 95%
73 and 95%
–
–
Diehl et al. (2001)
Daffodil, water birch and pussy willow pollens
25 µm (birch pollens)
Mass increase by up to a factor of 1.3 at 85%
2–~85%
≤0.002% (calculated)
Pope (2010)
Algal exudates (extracellular polymeric substances, EPS)
Artificial seawater with diatomaceaous and nanoplancton exudates
40–105 nm
~2.5 at 92%, lower than for artificial seawater devoid of exudates
45–92%
0.1 to 0.5% for sizes between 40 and 105 nm
–
Fuentes et al. (2011)
Artificial seawater with exudate of four different algal species
25–500 nm
~4 at 99%, lower than for artificial seawater devoid of exudates
75–99%
0.1 to 0.4% for diameters between 40 and 100 nm
–
Wex et al. (2010)
Fig. 5.
Ice nucleating number fraction fIN at the observed IN onset and maximum activity temperatures from the experiments listed in Table 6. For comparison, fIN data for immersion freezing on mineral dust (natural soil samples, median diameters of 0.2–1 µm) are included (M. Niemand, personal communication).
Table 6. Compilation of laboratory measurements of the IN properties of biological particles (n.a.=data not available)
Species
Highest T,°C where INA observed
Active number fraction or active IN per unit mass at highest INA temperature
Highest observed active fraction and corresponding temperature
Freezing mode (Immersion freezing = If, Contact freezing = Ctf, Condensation freezing = Cdf)
References
Bacteria isolated from air or precipitationPseudomonas fluorescens isolated from leaves, lake/stream water and/or snow
−10
0.02
0.94 (T=−16°C)
If
Maki and Willoughby (1978)
Unidentified microbacterium isolated from air above the Arctic Ocean
−4
0.05
1 (T = − 18°C)
If
Jayaweera and Flanagan (1982)
Pseudomonas sp. isolated from air above the Arctic Ocean
−9
0.1
n.a.
If
Jayaweera and Flanagan (1982)
Pseudomonas syringae isolated from rain and hail
−4
n.a.
n.a.
If
Sands et al. (1982)
Pseudomonas syringae and Erwinia herbicola isolated from air above plant canopies and bare soil
−10
n.a.
n.a.
If
Lindemann et al. (1982)
Pseudomonas syringae isolated from air and rainwater sampled over a soybean field
−5
n.a.
n.a.
If
Constantinidou et al. (1990)
Pseudomonas sp. isolated from cloud and rain water
−21 to −29
n.a.
n.a.
If
Ahern et al. (2007)
Pseudomonas syringae isolated from rain, snow, alpine streams, lakes and wild plants
−2 to −6
10−7
n.a.
If
Morris et al. (2008)
Microbacterium, Xanthomonas, Bacillus, Acinetobacter, Luteimonas, Stenotrophomonas and unspecified bacteria isolated from snow
−13 to −18
n.a.
n.a.
If
Mortazavi et al. (2008)
Bacteria isolated from air other habitats (list not exhaustive)Pseudomonas syringae
−5
2·10−6
5·10−5 (T = − 15°C)
If
Vali et al. (1976)
Pseudomonas syringae, different strains
–5
0.0043 to 10–7
n.a.
If
Gross et al. (1983)
Pseudomonas syringae strain 31R1
−1
10−8
0.5 (T = − 12°C)
If
Lindow et al. (1989)
Pseudomonas syringae
−8±1
0.0032
n.a.
If/Cdf
Möhler et al. (2008)
Pseudomonas viridiflava/Pseudomonas syringae mixture
−9.7
0.005
n.a.
If/Cdf
Möhler et al. (2008)
Pseudomonas syringae isolated from decaying alder leaves (Alnus tenuifolia)
−3
10−6
0.01(T = − 20°C)
If
Maki et al. (1974)
Pseudomonas sp. isolated from the guts of sub-Antartic beetles
−3.4
10−6
n.a.
If
Worland and Block (1999)
Pseudomonas Antarctica
−4
10−7
0.2 (T = − 10°C)
If
Obata et al. (1999)
Erwinia herbicola
−9±1
0.0007
n.a.
If/Cdf
Möhler et al. (2008)
Erwinia herbicola, cell-free centrifuged suspensions
−3
n.a.
n.a.
If
Phelps et al. (1986)
M1
−3
10−6
0.01 (T = − 10°C)
If
Yankofsky et al. (1981)
M1
−3
n.a.
n.a.
Ctf
Levin and Yankofsky (1983)
M1
−3
n.a.
n.a.
If
Levin and Yankofsky (1983)
Flavobacterium sp., Psychrobacter sp., and Sphingomonas sp. isolated from permafrost soil
n.a.
n.a.
4·10−7 (T = − 10°C)
If
Ponder et al. (2005)
Snomax
−5.6
0.01
0.23 (T = − 8±1°C)
If/Cdf
Möhler et al. (2008)
Snomax
−4
1.3·1012 g−1
5.5·1012 g−1 (T = − 12°C)
Cdf
Ward and DeMott (1989)
Snomax
−5.3
n.a.
n.a.
If
Wood et al. (2002)
Snomax
−26, Rhi = 116±6%
0.001–0.01
n.a.
Deposition nucleation (no experiments at warmer T)
Chernoff and Bertram (2010)
INA bacteria on oat leaves
−2.5
10−7
0.008 (T < − 4°C)
If
Hirano et al. (1985)
several representative Arctic and Antarctic sea-ice bacterial isolates
−40 to −42
n.a.
n.a.
If
Junge and Swanson (2008)
LichensRhizoplaca chrysoleuca (the most active of 15 investigated lichen species)
−2.3
103 g−1, grinded material
108 g−1 (T = − 3C), grinded material
If
Kieft (1988)
Psora decipiens (the least active of 15 investigated lichen species)
−8
103 g−1, grinded material
105 g−1 (T = − 12 °C), grinded material
If
Kieft (1988)
18 lichen mycobionts
−4.1 to −10
n.a.
n.a.
If
Kieft and Ahmadjian (1989)
Lecanora dispersa (lichen fungus)
−4.2
~104 g−1
~7·107 g−1 (T = − 8 °C)
If
Kieft and Ahmadjian (1989)
Cladonia cristatella (lichen fungus)
−6.3
~106 g−1
~5·106 g−1( (T = − 12 °C)
If
Kieft and Ahmadjian (1989)
Ascospora fuscata (lichen fungus)
−9.1
~2·104 g−1
~2·105 g−1 (T = − 12°C)
If
Kieft and Ahmadjian (1989)
Rhizoplaca chrysoleuca (lichen fungus), different clones
−4.6 to −4.8
104 to 2·105 g−1
~2·107 g−1 (T = − 12°C)
If
Kieft and Ahmadjian (1989)
13 lichen photobionts
−5.1 to −16
n.a.
n.a.
If
Kieft and Ahmadjian (1989)
Trebouxia incrustata (lichen photobiont)
−9.1
~2·104 g−1
~6·104 g−1 (T = − 12°C)
If
Kieft and Ahmadjian (1989)
Trebouxia erici (lichen photobiont)
−9.2
~6·105 g−1
~106 g−1 (T = − 12°C)
If
Kieft and Ahmadjian (1989)
Trebouxia sp. (lichen photobiont)
−6
~6·104 g−1
~106 g−1 (T = − 12°C)
If
Kieft and Ahmadjian (1989)
Unspecified lichen fragments from Norway, Faroe Islands, Ethiopia, UK, Australia, Antartica
−5.1
n.a.
n.a.
If
Henderson-Begg et al. (2009)
FungiPenicillium digitatum spores isolated from air
−10
0.01
n.a.
If
Jayaweera and Flanagan (1982)
Cladosporium herbarum spores isolated from air
−15
0.01
n.a.
If
Jayaweera and Flanagan (1982)
Penicillium notatum spores isolated from air
−22
0.01
n.a.
If
Jayaweera and Flanagan (1982)
Penicillium frequentes spores isolated from air
−22.5
0.01
n.a.
If
Jayaweera and Flanagan (1982)
Rhizopus stolonifera spores isolated from air
−23
0.01
n.a.
If
Jayaweera and Flanagan (1982)
Fusarium avanaceum
−2.5
105 g−1
1011 g−1 (T = − 10°C)
If
Pouleur et al. (1992)
Fusarium acuminatum
−5
n.a.
n.a.
If
Pouleur et al. (1992)
Fusarium sp. isolated from the guts of insect larvae
−5
n.a.
n.a.
If
Tsumuki et al. (1992)
Fusarium oxysporum (12 out of 42 isolates, from plants)
−1
n.a.
n.a.
If
Richard et al. (1996)
Fusarium tricinctum (8 out of 14 isolates, from plants and soil)
−1
n.a.
n.a.
If
Richard et al. (1996)
Cladosporium spores
−28.5
~0.002
0.2 to 1 (T = − 35°C)
If
Iannone et al. (2011)
Pollen
Pine pollen
−8
0.1
0.9 (T = − 18°C)
Cdf
Diehl et al. (2001)
Pine pollen
−16
n.a.
n.a.
If
Diehl et al. (2002)
Pine pollen
−12
n.a.
n.a.
Ctf
Diehl et al. (2002)
Birch pollen
−8
0.04
0.98 (T = − 18°C)
Cdf
Diehl et al. (2001)
Birch pollen
−10
n.a.
n.a.
If
Diehl et al. (2002)
Birch pollen
−6
n.a.
n.a.
Ctf
Diehl et al. (2002)
Oak pollen
−8
0.03
0.5 (T = − 18°C)
Cdf
Diehl et al. (2001)
Oak pollen
−14
n.a.
n.a.
If
Diehl et al. (2002)
Oak pollen
−10
n.a.
n.a.
Ctf
Diehl et al. (2002)
Grass pollen
−8
0.02
0.8 (T = − 18°C)
Cdf
Diehl et al. (2001)
Grass pollen
−14
n.a.
n.a.
If
Diehl et al. (2002)
Grass pollen
−10
n.a.
n.a.
Ctf
Diehl et al. (2002)
Alder pollen
−10
n.a.
n.a.
If
von Blohn et al. (2005)
Alder pollen
−10
n.a.
n.a.
Ctf
von Blohn et al. (2005)
Lombardy poplar pollen
−18
n.a.
n.a.
If
von Blohn et al. (2005)
Lombardy poplar pollen
−14
n.a.
n.a.
Ctf
von Blohn et al. (2005)
Redtop grass pollen
−16
n.a.
n.a.
If
von Blohn et al. (2005)
Redtop grass pollen
−16
n.a.
n.a.
Ctf
von Blohn et al. (2005)
Kentucky blue pollen
−14
n.a.
n.a.
If
von Blohn et al. (2005)
Kentucky blue pollen
−10
n.a.
n.a.
Ctf
von Blohn et al. (2005)
Various pollen, including crushed pollen
no IN observed
−
−
Deposition nucleation
Diehl et al. (2001)
Algae
25 algae species isolated from Antarctic soils
−5 (>-8 for 4 out of 25 species)
n.a.
n.a.
If
Worland and Lukesova (2000)
Seaweed (8 species)
−7
n.a.
n.a.
If
Lundheim (1997)
Leaf litter
Poplar mulch
−5
~105 g−1
~5·109 g−1 (T = − 15°C)
If
Schnell and Vali (1972)
Sage leaf litter
−6
~103 g−1
~107 g−1 (T = − 17°C)
If
Schnell and Vali (1972)
Green poplar leaves
−9
~2·102 g−1
~2·104 g−1 (T = − 17°C)
If
Schnell and Vali (1972)
Leaf litter of several trees and grasses in tropical climate zones
−7
~102 g−1
~4·104 g−1 (T = − 18°C)
If
Schnell and Vali (1976)
Leaf litter of several trees and grasses in humid mesothermal climate zones
−6
~102 g−1
~4·108 g−1 (T = − 23°C)
If
Schnell and Vali (1976)
Leaf litter of several trees and grasses in humid microthermal climate zones
−4
~102 g−1
~4·1010 g−1 (T = − 22°C)
If
Schnell and Vali (1976)
Tea leaf litter
−5
102 g−1
~5·104 g−1 (T = − 12°C)
If
Schnell and Tan-Schnell (1982)
PlanktonCachonina Niei
−3
102 g−1
~1 (T = − 14°C); 106 g−1 (T = − 10°C)
If
Schnell (1975)
Ochromonus danica and Porphyridium aerugineum
>− 15
n.a.
n.a.
If
Schnell (1975)
Unspecified mixture of 95% phytoplankton, 5% zooplankton and associated debris
−3.5
102 g−1
106 g−1 (T = − 10°C)
If
Schnell and Vali (1975)
AMS
Aerodyne Mass Spectrometer
ATOFMS
TSI Aerosol Time-of-Flight Mass Spectrometer
ATP
Adenosine Triphosphate
BAMS
Bioaerosol Mass Spectrometry
Bp
Base Pairs
BS
Break-Down Spectroscopy
CCN
Cloud Condensation Nuclei
CFU
Colony Forming Units
DAPI
4.6-diamidino-2-phenylindole
ddNTP
dideoxynucleotidetriphophate
DNA
Deoxyribonucleic Acid
dNTP
deoxynucleotidetriphosphate
EPS
Exopolymer Secretions
FBAP
Fluorescent Biological Aerosol Particles
FISH
Fluorescent in-situ hybridization
GF
Growth Factor
Hulis
Humic Like Substances
IN
Ice Nuclei
INA
Ice Nucleation Active
IPCC
Intergovernmental panel on climate change
ISI
Institute for Scientific Information
ITS
Internal Transcribed Spacer
LDD
Long Distance Dispersal
LIBS
Laser-Induced Breakdown Spectroscopy
LIDAR
LIght Detection And Ranging
MALDI-TOF
Matrix-Assisted Laser Desorption Ionization Time-of-Flight
MS
Mass Spectrometry
NCBI
National Center for Biotechnology Information
OC
Organic Carbon
PBAP
Primary Biological Aerosol Particles
PCR
Polymerase Chain Reaction
PIXE
Particle-Induced x-ray Emission
PM
Patriculate Matter
RH
Relative Humidity
RNA
Ribonucleic Acid
rRNA
Ribosomal RNA
SEM
Scanning Electron Microscopy
SIBS
Spark-Induced Breakdown Spectroscopy
SOA
Secondary Organic Aerosol
STXM
Scanning Transmission X-ray Microscopy with Near-Edge X-ray Absorption Fine Structure
TIRFM
Total Internal Reflection Fluorescence Microscopy
T-RFLP
Terminal Restriction Fragment Length Polymorphism
TSP
Total Suspended Particles
UV
Ultraviolet Light
UV-APS
Ultraviolet Aerodynamic Particle Sizer
WIBS
Wide Issue Bioaerosol Spectrometer
AMS
Aerodyne Mass Spectrometer
ATOFMS
TSI Aerosol Time-of-Flight Mass Spectrometer
ATP
Adenosine Triphosphate
BAMS
Bioaerosol Mass Spectrometry
Bp
Base Pairs
BS
Break-Down Spectroscopy
CCN
Cloud Condensation Nuclei
CFU
Colony Forming Units
DAPI
4.6-diamidino-2-phenylindole
ddNTP
dideoxynucleotidetriphophate
DNA
Deoxyribonucleic Acid
dNTP
deoxynucleotidetriphosphate
EPS
Exopolymer Secretions
FBAP
Fluorescent Biological Aerosol Particles
FISH
Fluorescent in-situ hybridization
GF
Growth Factor
Hulis
Humic Like Substances
IN
Ice Nuclei
INA
Ice Nucleation Active
IPCC
Intergovernmental panel on climate change
ISI
Institute for Scientific Information
ITS
Internal Transcribed Spacer
LDD
Long Distance Dispersal
LIBS
Laser-Induced Breakdown Spectroscopy
LIDAR
LIght Detection And Ranging
MALDI-TOF
Matrix-Assisted Laser Desorption Ionization Time-of-Flight
MS
Mass Spectrometry
NCBI
National Center for Biotechnology Information
OC
Organic Carbon
PBAP
Primary Biological Aerosol Particles
PCR
Polymerase Chain Reaction
PIXE
Particle-Induced x-ray Emission
PM
Patriculate Matter
RH
Relative Humidity
RNA
Ribonucleic Acid
rRNA
Ribosomal RNA
SEM
Scanning Electron Microscopy
SIBS
Spark-Induced Breakdown Spectroscopy
SOA
Secondary Organic Aerosol
STXM
Scanning Transmission X-ray Microscopy with Near-Edge X-ray Absorption Fine Structure
TIRFM
Total Internal Reflection Fluorescence Microscopy
T-RFLP
Terminal Restriction Fragment Length Polymorphism
TSP
Total Suspended Particles
UV
Ultraviolet Light
UV-APS
Ultraviolet Aerodynamic Particle Sizer
WIBS
Wide Issue Bioaerosol Spectrometer