TY - JOUR
T1 - Eddy covariance emission and deposition flux measurements using proton transfer reaction – time of flight – mass spectrometry (PTR-TOF-MS): comparison with PTR-MS measured vertical gradients and fluxes
AU - Park, J.H.
AU - Goldstein, A.H.
AU - Timkovsky, J
AU - Fares, S.
AU - Weber, R.
AU - Karlik, J.
AU - Holzinger, R.
PY - 2013
Y1 - 2013
N2 - During summer 2010, a proton transfer reaction
– time of flight – mass spectrometer (PTR-TOF-MS)
and a quadrupole proton transfer reaction mass spectrometer
(PTR-MS) were deployed simultaneously for one month
in an orange orchard in the Central Valley of California to
collect continuous data suitable for eddy covariance (EC)
flux calculations. The high time resolution (5 Hz) and high
mass resolution (up to 5000 m/1m) data from the PTRTOF-
MS provided the basis for calculating the concentration
and flux for a wide range of volatile organic compounds
(VOC). Throughout the campaign, 664 mass peaks
were detected in mass-to-charge ratios between 10 and
1278. Here we present PTR-TOF-MS EC fluxes of the 27
ion species for which the vertical gradient was simultaneously
measured by PTR-MS. These EC flux data were validated
through spectral analysis (i.e., co-spectrum, normalized
co-spectrum, and ogive). Based on inter-comparison of
the two PTR instruments, no significant instrumental biases
were found in either mixing ratios or fluxes, and the data
showed agreement within 5% on average for methanol and
acetone. For the measured biogenic volatile organic compounds
(BVOC), the EC fluxes from PTR-TOF-MS were
in agreement with the qualitatively inferred flux directions
from vertical gradient measurements by PTR-MS. For the
27 selected ion species reported here, the PTR-TOF-MS
measured total (24 h) mean net flux of 299 μg Cm−2 h−1.
The dominant BVOC emissions from this site were
monoterpenes (m/z 81.070 +m/z 137.131 +m/z 95.086,
34 %, 102 μg Cm−2 h−1) and methanol (m/z 33.032, 18 %,
72 μgCm−2 h−1). The next largest fluxes were detected
at the following masses (attribution in parenthesis): m/z
59.048 (mostly acetone, 12.2 %, 36.5 μgCm−2 h−1), m/z
61.027 (mostly acetic acid, 11.9 %, 35.7 μg Cm−2 h−1), m/z
93.069 (para-cymene + toluene, 4.1 %, 12.2 μgCm−2 h−1),
m/z 45.033 (acetaldehyde, 3.8 %, 11.5 μgCm−2 h−1),
m/z 71.048 (methylvinylketone + methacrolein, 2.4 %,
7.1 μgCm−2 h−1), and m/z 69.071 (isoprene + 2-methyl-
3-butene-2-ol, 1.8 %, 5.3 μg Cm−2 h−1). Low levels of emission
and/or deposition (
AB - During summer 2010, a proton transfer reaction
– time of flight – mass spectrometer (PTR-TOF-MS)
and a quadrupole proton transfer reaction mass spectrometer
(PTR-MS) were deployed simultaneously for one month
in an orange orchard in the Central Valley of California to
collect continuous data suitable for eddy covariance (EC)
flux calculations. The high time resolution (5 Hz) and high
mass resolution (up to 5000 m/1m) data from the PTRTOF-
MS provided the basis for calculating the concentration
and flux for a wide range of volatile organic compounds
(VOC). Throughout the campaign, 664 mass peaks
were detected in mass-to-charge ratios between 10 and
1278. Here we present PTR-TOF-MS EC fluxes of the 27
ion species for which the vertical gradient was simultaneously
measured by PTR-MS. These EC flux data were validated
through spectral analysis (i.e., co-spectrum, normalized
co-spectrum, and ogive). Based on inter-comparison of
the two PTR instruments, no significant instrumental biases
were found in either mixing ratios or fluxes, and the data
showed agreement within 5% on average for methanol and
acetone. For the measured biogenic volatile organic compounds
(BVOC), the EC fluxes from PTR-TOF-MS were
in agreement with the qualitatively inferred flux directions
from vertical gradient measurements by PTR-MS. For the
27 selected ion species reported here, the PTR-TOF-MS
measured total (24 h) mean net flux of 299 μg Cm−2 h−1.
The dominant BVOC emissions from this site were
monoterpenes (m/z 81.070 +m/z 137.131 +m/z 95.086,
34 %, 102 μg Cm−2 h−1) and methanol (m/z 33.032, 18 %,
72 μgCm−2 h−1). The next largest fluxes were detected
at the following masses (attribution in parenthesis): m/z
59.048 (mostly acetone, 12.2 %, 36.5 μgCm−2 h−1), m/z
61.027 (mostly acetic acid, 11.9 %, 35.7 μg Cm−2 h−1), m/z
93.069 (para-cymene + toluene, 4.1 %, 12.2 μgCm−2 h−1),
m/z 45.033 (acetaldehyde, 3.8 %, 11.5 μgCm−2 h−1),
m/z 71.048 (methylvinylketone + methacrolein, 2.4 %,
7.1 μgCm−2 h−1), and m/z 69.071 (isoprene + 2-methyl-
3-butene-2-ol, 1.8 %, 5.3 μg Cm−2 h−1). Low levels of emission
and/or deposition (
U2 - 10.5194/acp-13-1439-2013
DO - 10.5194/acp-13-1439-2013
M3 - Article
SN - 1680-7316
VL - 13
SP - 1439
EP - 1456
JO - Atmospheric chemistry and physics
JF - Atmospheric chemistry and physics
ER -