Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways
Air samples collected during 1994–2000 at the Canadian Arctic air monitoring station Alert (82°30' N, 62°20' W) were analysed by enantiospecific gas chromatography–mass spectrometry for α-hexachlorocyclohexane (α-HCH), <i>trans</i>-chlordane (TC) and <i>cis</i>-chlo...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Copernicus Publications
2015-02-01
|
Series: | Atmospheric Chemistry and Physics |
Online Access: | http://www.atmos-chem-phys.net/15/1411/2015/acp-15-1411-2015.pdf |
id |
doaj-40d21f342824423ab4b7f233cd8101ad |
---|---|
record_format |
Article |
spelling |
doaj-40d21f342824423ab4b7f233cd8101ad2020-11-24T22:48:54ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242015-02-011531411142010.5194/acp-15-1411-2015Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathwaysT. F. Bidleman0L. M. Jantunen1H. Hung2J. Ma3G. A. Stern4B. Rosenberg5J. Racine6Department of Chemistry, Umeå University, 901 87 Umeå, SwedenAir Quality Processes Research Section, Environment Canada, 6248 Eighth Line, Egbert, ON, L0L 1N0, CanadaAir Quality Processes Research Section, Environment Canada, 4905 Dufferin St., Toronto, ON, M3H 5T4, CanadaKey Laboratory of Western China's Environmental System, Ministry of Education, College of Earth and Environment Sciences, Lanzhou University, Lanzhou, ChinaCentre for Earth Observation Science, University of Manitoba, 474 Wallace Building, 125 Dysard Road, Winnipeg, MB, R3T 2N2, CanadaFreshwater Institute, Department of Fisheries and Oceans, University of Manitoba, 501 University Crescent, Winnipeg, MB, R3T 2N6, CanadaAir Quality Modelling Application Section, Canadian Meteorological Centre, 2121 Trans-Canada Highway, Dorval, QC, H9P 1J3, CanadaAir samples collected during 1994–2000 at the Canadian Arctic air monitoring station Alert (82°30' N, 62°20' W) were analysed by enantiospecific gas chromatography–mass spectrometry for α-hexachlorocyclohexane (α-HCH), <i>trans</i>-chlordane (TC) and <i>cis</i>-chlordane (CC). Results were expressed as enantiomer fractions (EF = peak areas of (+)/[(+) + (−)] enantiomers), where EFs = 0.5, < 0.5 and > 0.5 indicate racemic composition, and preferential depletion of (+) and (−) enantiomers, respectively. Long-term average EFs were close to racemic values for α -HCH (0.504 ± 0.004, <i>n</i> = 197) and CC (0.505 ± 0.004, <i>n</i> = 162), and deviated farther from racemic for TC (0.470 ± 0.013, <i>n</i> = 165). Digital filtration analysis revealed annual cycles of lower α-HCH EFs in summer–fall and higher EFs in winter–spring. These cycles suggest volatilization of partially degraded α-HCH with EF < 0.5 from open water and advection to Alert during the warm season, and background transport of α-HCH with EF > 0.5 during the cold season. The contribution of sea-volatilized α-HCH was only 11% at Alert, vs. 32% at Resolute Bay (74.68° N, 94.90° W) in 1999. EFs of TC also followed annual cycles of lower and higher values in the warm and cold seasons. These were in phase with low and high cycles of the TC/CC ratio (expressed as F<sub>TC</sub> = TC/(TC+CC)), which suggests greater contribution of microbially "weathered" TC in summer–fall versus winter–spring. CC was closer to racemic than TC and displayed seasonal cycles only in 1997–1998. EF profiles are likely to change with rising contribution of secondary emission sources, weathering of residues in the environment, and loss of ice cover in the Arctic. Enantiomer-specific analysis could provide added forensic capability to air monitoring programs.http://www.atmos-chem-phys.net/15/1411/2015/acp-15-1411-2015.pdf |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
T. F. Bidleman L. M. Jantunen H. Hung J. Ma G. A. Stern B. Rosenberg J. Racine |
spellingShingle |
T. F. Bidleman L. M. Jantunen H. Hung J. Ma G. A. Stern B. Rosenberg J. Racine Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways Atmospheric Chemistry and Physics |
author_facet |
T. F. Bidleman L. M. Jantunen H. Hung J. Ma G. A. Stern B. Rosenberg J. Racine |
author_sort |
T. F. Bidleman |
title |
Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways |
title_short |
Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways |
title_full |
Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways |
title_fullStr |
Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways |
title_full_unstemmed |
Annual cycles of organochlorine pesticide enantiomers in Arctic air suggest changing sources and pathways |
title_sort |
annual cycles of organochlorine pesticide enantiomers in arctic air suggest changing sources and pathways |
publisher |
Copernicus Publications |
series |
Atmospheric Chemistry and Physics |
issn |
1680-7316 1680-7324 |
publishDate |
2015-02-01 |
description |
Air samples collected during 1994–2000 at the Canadian Arctic air
monitoring station Alert (82°30' N, 62°20' W) were analysed by enantiospecific gas chromatography–mass
spectrometry for α-hexachlorocyclohexane (α-HCH),
<i>trans</i>-chlordane (TC) and <i>cis</i>-chlordane (CC). Results were expressed as enantiomer
fractions (EF = peak areas of (+)/[(+) + (−)] enantiomers), where
EFs = 0.5, < 0.5 and > 0.5 indicate racemic
composition, and preferential depletion of (+) and (−) enantiomers,
respectively. Long-term average EFs were close to racemic values for α
-HCH (0.504 ± 0.004, <i>n</i> = 197) and CC (0.505 ± 0.004, <i>n</i> = 162), and deviated farther
from racemic for TC (0.470 ± 0.013, <i>n</i> = 165). Digital filtration analysis revealed annual cycles of
lower α-HCH EFs in summer–fall and higher EFs in winter–spring. These cycles
suggest volatilization of partially degraded α-HCH with EF < 0.5 from open water and advection to Alert during the warm season, and
background transport of α-HCH with EF > 0.5 during the
cold season. The contribution of sea-volatilized α-HCH was only
11% at Alert, vs. 32% at Resolute Bay (74.68° N,
94.90° W) in 1999. EFs of TC also followed annual cycles of lower
and higher values in the warm and cold seasons. These were in phase with low
and high cycles of the TC/CC ratio (expressed as F<sub>TC</sub> = TC/(TC+CC)),
which suggests greater contribution of microbially "weathered" TC in
summer–fall versus winter–spring. CC was closer to racemic than TC and
displayed seasonal cycles only in 1997–1998. EF profiles are likely to
change with rising contribution of secondary emission sources, weathering of
residues in the environment, and loss of ice cover in the Arctic.
Enantiomer-specific analysis could provide added forensic capability to air
monitoring programs. |
url |
http://www.atmos-chem-phys.net/15/1411/2015/acp-15-1411-2015.pdf |
work_keys_str_mv |
AT tfbidleman annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways AT lmjantunen annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways AT hhung annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways AT jma annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways AT gastern annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways AT brosenberg annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways AT jracine annualcyclesoforganochlorinepesticideenantiomersinarcticairsuggestchangingsourcesandpathways |
_version_ |
1725678265933234176 |