Atmospheric Deposition of Organochlorine Pesticides and Industrial Compounds to Seasonal Surface Snow at Four Glacier Sites on Svalbard, 2013–2014

2020 ◽  
Vol 54 (15) ◽  
pp. 9265-9273
Author(s):  
Mark H. Hermanson ◽  
Elisabeth Isaksson ◽  
Richard Hann ◽  
Camilla Teixeira ◽  
Derek C. G. Muir
1986 ◽  
Vol 21 (2) ◽  
pp. 251-256 ◽  
Author(s):  
Robert C. McCrea ◽  
Greg M. Wickware

Abstract Peatland waters of the Moose River basin, as well as surficial sediments and vascular plants of the estuary were sampled in 1982. Elevated levels of PCBs were found at all five peatland sites; concentrations ranged from 28 to 65 ng/L. Of the seventeen organochlorine pesticides investigated, the hexachlorocyclohexane isomers (a-and y-BHC) were the most prominent with total BHC concentrations ranging from 1.5 to 13.7 ng/L. The presence of these contaminants in ombrotrophic bogs indicated that there was atmospheric deposition of organochlorine contaminants in the basin. Analyses of surficial sediments, collected from tidal flats and coastal marshes, showed that PCBs and organochlorine pesticides were not present. Samples of Triglochin maritima L. seed heads and Typha latifolia L. roots were also free of PCBs.


2020 ◽  
Author(s):  
Jiayue Huang ◽  
Lyatt Jaeglé ◽  
Qianjie Chen ◽  
Becky Alexander ◽  
Tomás Sherwen ◽  
...  

Abstract. We use the GEOS-Chem chemical transport model to examine the influence of bromine release from blowing snow sea salt aerosol (SSA) on springtime bromine activation and O3 depletion events (ODEs) in the Arctic lower troposphere. We evaluate our simulation against observations of tropospheric BrO vertical column densities (VCDtropo) from the GOME-2 and OMI spaceborne instruments for three years (2007–2009), as well as against surface observations of O3. We conduct a simulation with blowing snow SSA emissions from first-year sea ice (FYI, with a surface snow salinity of 0.1 psu) and multi-year sea ice (MYI, with a surface snow salinity of 0.05 psu), assuming a factor of 5 bromide enrichment of surface snow relative to seawater. This simulation captures the magnitude of observed March–April GOME-2 and OMI VCDtropo to within 17 %, as well as their spatiotemporal variability (r = 0.76-0.85). Many of the large-scale bromine explosions are successfully reproduced, with the exception of events in May, which are absent or systematically underpredicted in the model. If we assume a lower salinity on MYI (0.01 psu) some of the bromine explosions events observed over MYI are not captured, suggesting that blowing snow over MYI is an important source of bromine activation. We find that the modeled atmospheric deposition onto snow-covered sea ice becomes highly enriched in bromide, increasing from enrichment factors of ~ 5 in September–February to 10–60 in May, consistent with freshly fallen snow composition observations. We propose that this progressive enrichment in deposition could enable blowing snow-induced halogen activation to propagate into May and might explain our late-spring underestimate in VCDtropo. We estimate that atmospheric deposition of SSA could increase snow salinity by up to 0.04 psu between February and April, which could be an important source of salinity for surface snow on MYI as well as FYI covered by deep snowpack. Inclusion of halogen release from blowing snow SSA in our simulations decreases monthly mean Arctic surface O3 by 4–8 ppbv (15–30 %) in March and 8–14 ppbv (30–40 %) in April. We reproduce a transport event of depleted O3 Arctic air down to 40º N observed at many sub-Arctic surface sites in early April 2007. While our simulation captures a few ODEs observed at coastal Arctic surface sites, it underestimates the magnitude of other events and entirely misses some events. We suggest that inclusion of direct snowpack activation, which is a strong local source of Br radicals in the shallow Arctic boundary layer, could help reconcile the success of our simulation at capturing satellite retrievals of VCDtropo with its difficulty in reproducing local ODEs.


2012 ◽  
Vol 433 ◽  
pp. 290-295 ◽  
Author(s):  
Jung-Ho Kang ◽  
Min-Hee Son ◽  
Soon Do Hur ◽  
Sungmin Hong ◽  
Hideaki Motoyama ◽  
...  

1970 ◽  
Vol 53 (2) ◽  
pp. 251-261
Author(s):  
G E Bagley ◽  
W L Reichel ◽  
E Cromartie

Abstract Polychlorinated biphenyls are widely used industrial compounds marketed in the United States under the trade name Aroclor. They have appeared in fish and wildlife tissues in this country and in Europe. They are known to be toxic, but more importantly, their presence in samples along with the commonly occurring organochlorine pesticides complicates the analysis to a serious degree, making i denti fication of pesticide residues by GLC without preliminary separation extremely unreliable. Residues of both polychlorinated biphenyls and organochlorine pesticides were present in eagle carcasses. Many of the polychlorinated biphenyl components had retention times identical with those of certain organochlorine pesticide residues. Identification was accomplished by preliminary separationson thin layer plates followed by combined GLC-mass spectrometry.


Chemosphere ◽  
2020 ◽  
Vol 243 ◽  
pp. 125324 ◽  
Author(s):  
Mark H. Hermanson ◽  
Elisabeth Isaksson ◽  
Dmitry Divine ◽  
Camilla Teixeira ◽  
Derek C.G. Muir

Sign in / Sign up

Export Citation Format

Share Document