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1.	Okeme, Joseph, et al. (author) Gas chromatographic estimation of vapor pressures and octanol-air partition coefficients of semivolatile organic compounds of emerging concern 2020 In: Journal of Chemical and Engineering Data. - Washington, DC, USA : American Chemical Society (ACS). - 0021-9568 .- 1520-5134. ; 65:5, s. 2467-2475 Journal article (peer-reviewed)abstract The subcooled liquid-phase vapor pressures (pL298/Pa) and octanol–air partition coefficients (KOA298) at T/K = 298, enthalpies of vaporization (ΔVAPH/kJ·mol–1), and internal energies of phase transfer from octanol to air (ΔOAU/kJ·mol–1) were estimated for synthetic musks, novel brominated flame retardants (N-BFR), organophosphate esters, and ultraviolet filters using the capillary gas chromatographic retention time (GC-RT) method. These compounds, which spanned approximately six and three orders of magnitude for pL298/Pa and KOA298, respectively, were co-chromatographed with one of three reference compounds to give initial estimates of properties at T/K = 298. The initial GC-RT property estimates were subsequently calibrated using 18 compounds that spanned 6 log units for pL298/Pa and 13 compounds covering 4 log units for KOA298. The calibrated log10pL298/Pa values estimated here ranged from 0.14 ± 0.19 to −9.19 ± 0.29 for cyclopentadecanone to syn-dechlorane plus (syn-DDC-CO), respectively, while the range of log10KOA298 values was 6.59 ± 0.26 to 11.40 ± 0.23 for cyclopentadecanone to 2,2′,4,4′,5-pentabromodiphenyl ether (BDE-99), respectively. The calibrated GC-RT-derived values were highly correlated with, and were within an average of 0.70 log units of, the literature data for compounds with well-established pL298/Pa and KOA298 measured or derived using non-GC-RT methods. Nonpolar compounds were used in this study to estimate the target polar compound data, which may introduce systematic errors. However, the comparison of our GC-RT results against the literature non-GC-RT values shows that the GC-RT methods performed similarly well for estimating both polar and nonpolar target compounds studied in this work.
2.	Rodgers, Timothy F.M., et al. (author) Novel Bayesian Method to Derive Final Adjusted Values of Physicochemical Properties : Application to 74 Compounds 2021 In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 55:18, s. 12302-12316 Journal article (peer-reviewed)abstract Accurate values of physicochemical properties are essential for screening semivolatile organic compounds for human and environmental hazard and risk. In silico approaches for estimation are widely used, but the accuracy of these and measured values can be difficult to ascertain. Final adjusted values (FAVs) harmonize literature-reported measurements to ensure consistency and minimize uncertainty. We propose a workflow, including a novel Bayesian approach, for estimating FAVs that combines measurements using direct and indirect methods and in silico values. The workflow was applied to 74 compounds across nine classes to generate recommended FAVs (FAVRs). Estimates generated by in silico methods (OPERA, COSMOtherm, EPI Suite, SPARC, and polyparameter linear free energy relationships (pp-LFER) models) differed by orders of magnitude for some properties and compounds and performed systematically worse for larger, more polar compounds. COSMOtherm and OPERA generally performed well with low bias although no single in silico method performed best across all compound classes and properties. Indirect measurement methods produced highly accurate and precise estimates compared with direct measurement methods. Our Bayesian method harmonized measured and in silico estimated physicochemical properties without introducing observable biases. We thus recommend use of the FAVRs presented here and that the proposed Bayesian workflow be used to generate FAVRs for SVOCs beyond those in this study.
3.	Bidleman, Terry F., et al. (author) Air-surface exchange of halomethoxybenzenes in a Swedish subarctic catchment 2024 In: Science of the Total Environment. - : Elsevier. - 0048-9697 .- 1879-1026. ; 948 Journal article (peer-reviewed)abstract Halomethoxybenzenes (HMBs) and related halomethoxyphenols are produced naturally in the marine and terrestrial environment and some also have anthropogenic origins. They are relatively volatile and water soluble and undergo atmospheric exchange with water bodies and soil. Here we report air-surface exchange of HMB compounds brominated anisoles and chlorinated dimethoxybenzenes in a Subarctic lake and catchment in Sweden during September 2022. HMBs were isolated from water on solid-phase extraction cartridges and from ground litter/soil by solvent extraction and determined by capillary gas chromatography - quadrupole mass spectrometry. Identified compounds in lake and stream water in the 10–100 pg L−1 range were 1,2,4,5-tetrachloro-3,6-dimethoxybenzene (DAME) > 2,4-dibromoanisole (DiBA) ≥ 2,4,6-tribromoanisole (TriBA) > 1,2,3,4-tetrachloro-5,6-dimethoxybenzene (tetrachloroveratrole, TeCV). DAME and the related compound 2,3,5,6-tetrachloro-4-methoxyphenol (DA) are reported in Subarctic litter/soil in the range 0.005–1.1 mg kg−1 dry weight (dw), whereas DiBA and TriBA were not detected in any litter/soil sample and TeCV in only one. Exchanges were assessed from concentrations in water and soil, air concentrations from a monitoring station at Pallas, Finland, and the physicochemical properties of the HMBs. Fluxes to and from the lake were estimated using the two-film gas exchange model. Net loadings (deposition minus volatilization) for the month of September were − 23, −15 and − 68 g for DiBA, TriBA and DAME, respectively, which amounted to about 4–7 % of the estimated lake inventory. An exchange assessment for DAME from litter/soil showed significant net volatilization at five sites, net deposition at one site and near-equilibrium at one site. The Torneträsk catchment appeared close to steady state with respect to HMB exchange during September 2022. The situation could be different during the warmer and colder seasons, and extending the study to cover these periods is a suggested next step.
4.	Bidleman, Terry F., et al. (author) Air-water exchange of brominated anisoles in the northern baltic sea 2014 In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 48:11, s. 6124-6132 Journal article (peer-reviewed)abstract Bromophenols produced by marine algae undergo O-methylation to form bromoanisoles (BAs), which are exchanged between water and air. BAs were determined in surface water of the northern Baltic Sea (Gulf of Bothnia, consisting of Bothnian Bay and Bothnian Sea) during 2011-2013 and on a transect of the entire Baltic in September 2013. The abundance decreased in the following order: 2,4,6-tribromoanisole (2,4,6-TBA) > 2,4-dibromoanisole (2,4-DBA) ≫ 2,6-dibromoanisole (2,6-DBA). Concentrations of 2,4-DBA and 2,4,6-TBA in September were higher in the southern than in the northern Baltic and correlated well with the higher salinity in the south. This suggests south-to-north advection and dilution with fresh riverine water enroute, and/or lower production in the north. The abundance in air over the northern Baltic also decreased in the following order: 2,4,6-TBA > 2,4-DBA. However, 2,6-DBA was estimated as a lower limit due to breakthrough from polyurethane foam traps used for sampling. Water/air fugacity ratios ranged from 3.4 to 7.6 for 2,4-DBA and from 18 to 94 for 2,4,6-TBA, indicating net volatilization. Flux estimates using the two-film model suggested that volatilization removes 980-1360 kg of total BAs from Bothnian Bay (38000 km(2)) between May and September. The release of bromine from outgassing of BAs could be up to 4-6% of bromine fluxes from previously reported volatilization of bromomethanes and bromochloromethanes.
5.	Bidleman, Terry F., et al. (author) Atmospheric transport and deposition of bromoanisoles along a temperate to arctic gradient 2017 In: Environmental Science and Technology. - Washington : American Chemical Society (ACS). - 1086-931X .- 1520-6912 .- 0013-936X .- 1520-5851. ; 51:19, s. 10974-10982 Journal article (peer-reviewed)abstract Bromoanisoles (BAs) arise from O-methylation of bromophenols, produced by marine algae and invertebrates. BAs undergo sea-air exchange and are transported over the oceans. Here we report 2,4-DiBA and 2,4,6-TriBA in air and deposition on the Swedish west coast (Råö) and the interior of arctic Finland (Pallas). Results are discussed in perspective with previous measurements in the northern Baltic region in 2011−2013. BAs in air decreased from south to north in the order Råö > northern Baltic > Pallas. Geometric mean concentrations at Pallas increased signiﬁcantly (p < 0.05) between 2002 and 2015 for 2,4-DiBA but not for 2,4,6-TriBA. The logarithm of BA partial pressures correlated signiﬁcantly to reciprocal air temperature at the coastal station Råö and over the Baltic, but only weakly (2,4-DiBA) or not signiﬁcantly (2,4,6-TriBA) at inland Pallas. Deposition ﬂuxes of BAs were similar at both sites despite lower air concentrations at Pallas, due to greater precipitation scavenging at lower temperatures. Proportions of the two BAs in air and deposition were related to Henry’s law partitioning and source regions. Precipitation concentrations were 10−40% of those in surface water of Bothnian Bay, northern Baltic Sea. BAs deposited in the bay catchment likely enter rivers and provide an unexpected source to northern estuaries. BAs may be precursors to higher molecular weight compounds identiﬁed by others in Swedish inland lakes.
6.	Bidleman, Terry F., et al. (author) Biannual cycles of organochlorine pesticide enantiomers in arctic air suggest changing sources and pathways 2014 In: Atmospheric Chemistry and Physics Discussions. - : Copernicus GmbH. - 1680-7367 .- 1680-7375. ; 14:17, s. 25027-25050 Journal article (peer-reviewed)abstract Air samples collected during 1994–2000 at the Canadian arctic air monitoring stationAlert (82300 N, 62200 W) were analyzed by enantiospecific gas chromatography –mass spectrometry for -hexachlorocyclohexane (-HCH), trans-chlordane (TC) and5 cis-chlordane (CC). Results were expressed as enantiomer fractions (EF = quantitiesof (+)/[(+)+(−)] enantiomers), where EFs=0.5, < 0.5 and > 0.5 indicate racemic composition,and preferential depletion of (+) and (−) enantiomers, respectively. Long-termaverage EFs were close to racemic values for -HCH (0.504±0.004, n =197) andCC (0.505±0.004, n =162), and deviated farther from racemic for TC (0.470±0.013,10 n =165). Digital filtration analysis revealed biannual cycles of lower -HCH EFs insummer-fall and higher EFs in winter-spring. These cycles suggest volatilization ofpartially degraded -HCH with EF < 0.5 from open water and advection to Alert duringthe warm season, and background transport of -HCH with EF> 0.5 during the coldseason. The contribution of sea-volatilized -HCH was only 11% at Alert, vs. 32%15 at Resolute Bay (74.68 N, 94.90W) in 1999. EFs of TC also followed biannual cyclesof lower and higher values in the warm and cold seasons. These were in phasewith low and high cycles of the TC/CC ratio (expressed as FTC =TC/(TC+CC)), whichsuggests greater contribution of microbially “weathered” TC in summer-fall vs. winterspring.CC was closer to racemic than TC and displayed seasonal cycles only in 1997–20 1998. EF profiles are likely to change with rising contribution of secondary emissionsources, weathering of residues in the environment, and loss of ice cover in the Arctic.Enantiomer-specific analysis could provide added forensic capability to air monitoringprograms.
7.	Bidleman, Terry F., et al. (author) Breakthrough during air sampling with polyurethane foam : What do PUF 2/PUF 1 ratios mean? 2018 In: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 192, s. 267-271 Journal article (peer-reviewed)abstract Frontal chromatography theory is applied to describe movement of gaseous semivolatile organic compounds (SVOCs) through a column of polyurethane foam (PUF). Collected mass fractions (FC) are predicted for sample volume/breakthrough volume ratios (τ = VS/VB) up to 6.0 and PUF bed theoretical plate numbers (N) from 2 to 16. The predictions assume constant air concentrations and temperatures. Extension of the calculations is done to relate the collection efficiency of a 2-PUF train (FC1+2) to the PUF 2/PUF 1 ratio. FC1+2 exceeds 0.9 for PUF 2/PUF 1 ≤ 0.5 and lengths of PUF commonly used in air samplers. As the PUF 2/PUF 1 ratio approaches unity, confidence in these predictions is limited by the analytical ability to distinguish residues on the two PUFs. Field data should not be arbitrarily discarded because some analytes broke through to the backup PUF trap. The fractional collection efficiencies can be used to estimate air concentrations from quantities retained on the PUF trap when sampling is not quantitative.
8.	Bidleman, Terry F., et al. (author) Bromoanisoles and Methoxylated Bromodiphenyl Ethers in Macroalgae from Nordic Coastal Regions 2019 In: Environmental Science. - London : Royal Society of Chemistry. - 2050-7887 .- 2050-7895. ; , s. 881-892 Journal article (peer-reviewed)abstract Marine macroalgae are used worldwide for human consumption, animal feed, cosmetics and agriculture. In addition to beneficial nutrients, macroalgae contain halogenated natural products (HNPs), some of which have toxic properties similar to those of well-known anthropogenic contaminants. Sixteen species of red, green and brown macroalgae were collected in 2017–2018 from coastal waters of the northern Baltic Sea, Sweden Atlantic and Norway Atlantic, and analyzed for bromoanisoles (BAs) and methoxylated bromodiphenyl ethers (MeO-BDEs). Target compounds were quantified by gas chromatography-low resolution mass spectrometry (GC-LRMS), with qualitative confirmation in selected species by GC-high resolution mass spectrometry (GC-HRMS). Quantified compounds were 2,4-diBA, 2,4,6-triBA, 2′-MeO-BDE68, 6-MeO-BDE47, and two tribromo-MeO-BDEs and one tetrabromo-MeO-BDE with unknown bromine substituent positions. Semiquantitative results for pentabromo-MeO-BDEs were also obtained for a few species by GC-HRMS. Three extraction methods were compared; soaking in methanol, soaking in methanol–dichloromethane, and blending with mixed solvents. Extraction yields of BAs did not differ significantly (p > 0.05) with the three methods and the two soaking methods gave equivalent yields of MeO-BDEs. Extraction efficiencies of MeO-BDEs were significantly lower using the blend method (p < 0.05). For reasons of simplicity and efficiency, the soaking methods are preferred. Concentrations varied by orders of magnitude among species: ∑2BAs 57 to 57 700 and ∑5MeO-BDEs < 10 to 476 pg g−1 wet weight (ww). Macroalgae standing out with ∑2BAs >1000 pg g−1 ww were Ascophyllum nodosum, Ceramium tenuicorne, Ceramium virgatum, Fucus radicans, Fucus serratus, Fucus vesiculosus, Saccharina latissima, Laminaria digitata, and Acrosiphonia/Spongomorpha sp. Species A. nodosum, C. tenuicorne, Chara virgata, F. radicans and F. vesiculosus (Sweden Atlantic only) had ∑5MeO-BDEs >100 pg g−1ww. Profiles of individual compounds showed distinct differences among species and locations.
9.	Bidleman, Terry F, et al. (author) Chiral persistent organic pollutants as tracers of atmospheric sources and fate : review and prospects for investigating climate change influences 2012 In: Atmospheric Pollution Research. - 1309-1042. ; 3:4, s. 371-382 Journal article (peer-reviewed)abstract Elimination of persistent organic pollutants (POPs) under national and international controls reduces “primary” emissions, but “secondary” emissions continue from residues deposited in soil, water, ice and vegetation during former years of high usage. Secondary sources are expected to dominate in the future, when POPs transport and accumulation will be controlled by air–surface exchange and the biogeochemical cycle of organic carbon. Climate change is likely to affect mobilization of POPs through, e.g., increased temperature, loss of ice cover in polar regions, melting glaciers and changes in soil and water microbiology which affect degradation and transformation. Chiral compounds offer advantages for following transport and fate pathways because of their ability to distinguish racemic (newly released or protected from microbial attack) and nonracemic (microbially altered) sources. Here we explain the rationale for this approach and suggest applications where chiral POPs could aid investigation of climate–mediated exchange and degradation processes. Examples include distinguishing agricultural vs. non–agricultural and recently used vs. residual pesticides, degradation and sequestration processes in soil, historical vs. recent atmospheric deposition, sources in arctic air and influence of ice cover on volatilization.
10.	Bidleman, Terry F, et al. (author) Chiral Pesticides in Soil and Water and Exchange with the Atmosphere 2002 In: TheScientificWorldJOURNAL. - : Hindawi Limited. ; 2, s. 357-373 Journal article (peer-reviewed)abstract The enantiomers of chiral pesticides are often metabolised at different rates in soil and water, leading to nonracemic residues. This paper reviews enantioselective metabolism of organochlorine pesticides (OCPs) in soil and water, and the use of enantiomers to follow transport and fate processes. Residues of chiral OCPs and their metabolites are frequently nonracemic in soil, although exceptions occur in which the OCPs are racemic. In soils where enantioselective degradation and/or metabolite formation has taken place, some OCPs usually show the same degradation preference — e.g., depletion of (+)trans-chlordane (TC) and (-)cis-chlordane (CC), and enrichment of the metabolite (+)heptachlor exo-epoxide (HEPX). The selectivity is ambivalent for other chemicals; preferential loss of either (+) or (-)o,p?-DDT and enrichment of either (+) or (-)oxychlordane (OXY) occurs in different soils. Nonracemic OCPs are found in air samples collected above soil which contains nonracemic residues. The enantiomer profiles of chlordanes in ambient air suggests that most chlordane in northern Alabama air comes from racemic sources (e.g., termiticide emissions), whereas a mixture of racemic and nonracemic (volatilisation from soil) sources supplies chlordane to air in the Great Lakes region. Chlordanes and HEPX are also nonracemic in arctic air, probably the result of soil emissions from lower latitudes. The (+) enantiomer of a-hexachlorocyclohexane (a-HCH) is preferentially metabolised in the Arctic Ocean, arctic lakes and watersheds, the North American Great Lakes, and the Baltic Sea. In some marine regions (the Bering and Chukchi Seas, parts of the North Sea) the preference is reversed and (-)a-HCH is depleted. Volatilisation from seas and large lakes can be traced by the appearance of nonracemic a-HCH in the air boundary layer above the water. Estimates of microbial degradation rates for a-HCH in the eastern Arctic Ocean and an arctic lake have been made from the enantiomer fractions (EFs) and mass balance in the water column. Apparent pseudo first-order rate constants in the eastern Arctic Ocean are 0.12 year-1 for (+)a-HCH, 0.030 year-1 for (-)a-HCH, and 0.037 year-1 for achiral ?-HCH. These rate constants are 3–10 times greater than those for basic hydrolysis in seawater. Microbial breakdown may compete with advective outflow for long-term removal of HCHs from the Arctic Ocean. Rate constants estimated for the arctic lake are about 3–8 times greater than those in the ocean.
11.	Bidleman, Terry F., et al. (author) Chlorinated pesticides and natural brominated anisoles in air at three northern Baltic stations 2017 In: Environmental Pollution. - : Elsevier. - 0269-7491 .- 1873-6424. ; 225, s. 381-389 Journal article (peer-reviewed)abstract Abstract Polyurethane foam (PUF) disk passive samplers were deployed at one inland and two island locations in the Bothnian Bay region of the northern Baltic Sea. Uptake was linear over 81–147 d and a temperature range of −2.6 to 14.2 °C for organochlorine pesticides (OCPs) and current-use pesticides (CUPs) having log KOA ≥9 at ambient temperatures. Partial saturation of the PUF disks occurred for the more volatile OCPs hexachlorocyclohexanes (HCHs) and hexachlorobenzene (HCB), and for bromoanisoles (BAs), which are products of bromophenols released by natural and anthropogenic sources. Correction for nonlinear uptake of these was made using experimentally measured PUF-air partition coefficients. Passive-derived air concentrations of pesticides were uniform over the bay and agreed within a factor of 2 or better with levels determined by active (pumped) sampling at one of the island stations. Levels of OCPs were similar to those reported at background sites in the European and Canadian Arctic and at monitoring stations in the central Baltic and southern Scandinavia, indicating long-range transport. The insecticide chlorpyrifos was 10 times lower at bay stations than in the Canadian Arctic. Insight to sources and processes was gained by examining compound profiles. Fractions Falpha = α-HCH/(α-HCH + γ-HCH) and FTC = trans-chlordane/(trans-chlordane + cis-chlordane) at bay stations were higher than in the Norwegian and Finnish Arctic and similar to those at the southern monitoring stations. Volatilization of chlordanes from Baltic seawater may also modify FTC. Higher FTriBA = 2,4,6-TriBA/(2,4,6-TriBA + 2,4-DiBA) distinguished local volatilization from the Baltic Sea versus lower FTriBA found at the inland site and reported in air on the Norwegian coast, suggesting westerly transport from the Atlantic across Norway and Sweden.
12.	Bidleman, Terry F., et al. (author) Drosophilin a methyl ether (DAME) and other chlorinated dimethoxybenzenes in fungi and forest litter from Sweden 2023 In: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 347 Journal article (peer-reviewed)abstract Fungi and substrates undergoing fungal decomposition were collected from forests in northern and southernSweden and analyzed for chlorinated dimethoxybenzenes (DMBs). Specimens were fungi fruiting bodies, rottingwood, forest litter and underlying humus. Targeted compounds were DAME (1,2,4,5-tetrachloro-3,6-DMB) andrelated fungal secondary metabolites. A screening procedure was developed which involved soaking the speci-mens in ethyl acetate followed by analysis by capillary gas chromatography – mass spectrometry with mass selec-tive detection (GC-MSD). DAME was the most frequently found (62% of 47 specimens) and often the most abun-dant target compound, with range and mean ± SD concentrations of <0.0017–3.81 and 0.21 ± 0.63 mg kg−1ww. Based on log-log correlations of partition coefficients of hydrophobic compounds between fungal biomass/water (KD) and octanol/water (KOW), five species of fungi are suggested to produce DAME de novo versus bioaccu-mulation from forest runoff water. Full-scan mass spectra of some high-concentration specimens indicated thepresence of a Cl2DMB and a Cl3DMB, which could not be identified further due to lack of standards, anddrosophilin A (DA = 2,3,5,6-tetrachloro-4-methoxyphenol), the precursor to DAME. Tetrachloroveratrole(TeCV = 1,2,3,4-tetrachloro-5,6-DMB) was found in only a few specimens. This study supports our hypothesis offungi as a source of DAME in terrestrial runoff and indicates that other chlorinated secondary metabolites arepresent. DAME is widely distributed globally, and it would be good to have a better understanding of its sourcesand pathways as a marker of terrestrial organochlorines and their availability for bioaccumulation
13.	Bidleman, Terry F., et al. (author) Field estimates of polyurethane foam : air partition coefficients for hexachlorobenzene, alpha-hexachlorocyclohexane and bromoanisoles 2016 In: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 159, s. 126-131 Journal article (peer-reviewed)abstract Partition coefficients of gaseous semivolatile organic compounds (SVOCs) between polyurethane foam (PUF) and air (KPA) are needed in the estimation of sampling rates for PUF disk passive air samplers. We determined KPA in field experiments by conducting long-term (24-48 h) air sampling to saturate PUF traps and shorter runs (2-4 h) to measure air concentrations. Sampling events were done at daily mean temperatures ranging from 1.9 to 17.5 °C. Target compounds were hexachlorobenzene (HCB), alpha-hexachlorocyclohexane (α-HCH), 2,4-dibromoanisole (2,4-DiBA) and 2,4,6-tribromoanisole (2,4,6-TriBA). KPA (mL g(-1)) was calculated from quantities on the PUF traps at saturation (ng g(-1)) divided by air concentrations (ng mL(-1)). Enthalpies of PUF-to-air transfer (ΔHPA, kJ mol(-1)) were determined from the slopes of log KPA/mL g(-1) versus 1/T(K) for HCB and the bromoanisoles, KPA of α-HCH was measured only at 14.3 to 17.5 °C and ΔHPA was not determined. Experimental log KPA/mL g(-1) at 15 °C were HCB = 7.37; α-HCH = 8.08; 2,4-DiBA = 7.26 and 2,4,6-TriBA = 7.26. Experimental log KPA/mL g(-1) were compared with predictions based on an octanol-air partition coefficient (log KOA) model (Shoeib and Harner, 2002a) and a polyparameter linear free relationship (pp-LFER) model (Kamprad and Goss, 2007) using different sets of solute parameters. Predicted KP values varied by factors of 3 to over 30, depending on the compound and the model. Such discrepancies provide incentive for experimental measurements of KPA for other SVOCs.
14.	Bidleman, Terry F., et al. (author) Forty-five years of foam : a retrospective on air sampling with polyurethane foam 2019 In: Bulletin of Environmental Contamination and Toxicology. - New York : Springer. - 0007-4861 .- 1432-0800. ; 102:4, s. 447-449 Journal article (peer-reviewed)
15.	Bidleman, Terry F., et al. (author) Is There Still “New” DDT in North America? An Investigation Using Proportions of DDT Compounds 2013 In: Occurrence, fate and impact of atmospheric pollutants on environmental and human health. - Washington, DC : American Chemical Society (ACS). - 9780841228900 - 9780841228917 ; , s. 153-181 Book chapter (peer-reviewed)abstract Usage of DDT ceased over four decades ago in Canada and the United States, and since 2000 in Mexico. Potential sources in the North American atmosphere today include emissions of legacy residues from soils and long-range transport from other countries where DDT is still used or recently banned. Distinction of source types is investigated here using proportions of p,p'-DDT, o,p'-DDT, p,p'-DDE and p,p'-DDD. The relative volatilization of DDT compounds can be accurately described by their subcooled liquid vapor pressures (PO; e.g., (p,p'-DDT/p,p'-DDE)AIR = (p,p'-DDT/p,p'-DDE)son. x PL, (DDT)/P-L,P-DDE. Using this model, the expected proportions in air due to volatilization from technical DDT and from soils in Canada, the U.S.A. and Mexico were estimated and expressed as the fractions F-DDTE = p,p'-DDT/(p,p'-DDT + P,P'-DDE), F-DDTO = p,p1-DDT/(p,p'-DDT + o,p'-DDT), and FDDTD = p,p1-DDT/(p,p'-DDT + p,p1-DDD). FDDTE, FDDTO and FDDTD predicted from soil emissions were compared to compound fractions in ambient air sampled at the Integrated Atmospheric Deposition Network (IADN) of stations on the Great Lakes between Canada and the U.S.A., and at arctic monitoring stations. FDDTE in air at IADN stations on lakes Erie, Ontario, Michigan and Huron were lower than in technical DDT vapor. This is consistent with emissions of aged residues from agricultural land and urban centers near these lakes. By comparison, FDDTE values were higher at stations on Lake Superior where atmospheric DDT is likely due to long-range transport rather than regional soil emissions. FDDTE increased from the early 1990s to 2005 at the Lake Superior stations and at the Canadian arctic station Alert between 2002-2005, whereas a significant decline in FDDTE was observed at the Norwegian arctic station Zeppelin Mountain. The mean FDDTO in air at IADN stations were consistent with either soil emissions or technical DDT composition, but annual values showed significant downward trends at two Canadian stations, and also decreased with time at Zeppelin Mountain (but not at Alert). These trends might signify contribution from dicofol-type DDT sources, which have a lower FDDTO than technical DDT or soil emissions, or preferential degradation of p,p'-DDT vs. o,p'-DDT over time. FDDTD in air at IADN stations were lower than in technical DDT vapor, showing the influence of soil sources. The enantiomer proportions of the chiral compounds o,p'-DDT and o,p1-DDD were nonracemic in some soils and ambient air, but enantiospecific analysis has not been done for IADN air samples. It is suggested that isomer, parent/metabolite and enantiomer composition information be incorporated into air monitoring programs to help identify sources.
16.	Bidleman, Terry F., et al. (author) Lake Superior Has Lost over 90% of Its Pesticide HCH Load since 1986 2021 In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 55:14, s. 9518-9526 Journal article (peer-reviewed)abstract The time trend of α- and γ-hexachlorocyclohexane (HCH) isomers in Lake Superior water was followed from 1986 to 2016, the longest record for any persistent organic pollutant (POP) in Great Lakes water. Dissipation of α-HCH and γ-HCHs was first order, with halving times (t1/2) of 5.7 and 8.5 y, respectively. Loss rates were not significantly different starting a decade later (1996−2016). Concentrations of β-HCH were followed from 1996−2016 and dissipated more slowly (t1/2 = 16 y). In 1986, the lake contained an estimated 98.8 tonnes of α-HCH and 13.2 tonnes of γ-HCH; by 2016, only 2.7% and 7.9% of 1986 quantities remained. Halving times of both isomers in water were longer than those reported in air, and for γ-HCH, they were longer in water than those reported in lake trout. Microbial degradation was evident by enantioselective depletion of (+)α-HCH, which increased from 1996 to 2011. Volatilization was the main removal process for both isomers, followed by degradation (hydrolytic and microbial) and outflow through the St. Mary’s River. Sedimentation was minor. Major uncertainties in quantifying removal processes were in the two-film model for predicting volatilization and in microbial degradation rates. The study highlights the value of long-term monitoring of chemicals in water to interpreting removal processes and trends in biota.
17.	Bidleman, Terry F. (author) Letter to the Editor regarding 'Celebrating Bidleman's 1988 "Atmospheric Processes" 2015 In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 49:5, s. 2586-2586 Journal article (peer-reviewed)
18.	Bidleman, Terry F., et al. (author) Sea-air exchange of bromoanisoles and methoxylated bromodiphenylethers in the Northern Baltic 2016 In: Marine Pollution Bulletin. - : Elsevier. - 0025-326X .- 1879-3363. ; 112:1-2, s. 58-64 Journal article (peer-reviewed)abstract Halogenated natural products in biota of the Baltic Sea include bromoanisoles (BAs) and methoxylated bromodiphenyl ethers (MeO-BDEs). We identified biogenic 6-MeO-BDE47 and 2'-MeO-BDE68 in Baltic water and air for the first time using gas chromatography - high resolution mass spectrometry. Partial pressures in air were related to temperature by: log p/Pa=m/T(K)+b. We determined Henry's law constants (HLCs) of 2,4-dibromoanisole (2,4-DiBA) and 2,4,6-tribromoanisole (2,4,6-TriBA) from 5 to 30°C and revised our assessment of gas exchange in the northern Baltic. The new water/air fugacity ratios (FRs) were lower, but still indicated net volatilization in May-June for 2,4-DiBA and May - September for 2,4,6-TriBA. The net flux (negative) of BAs from Bothnian Bay (38,000km2) between May - September was revised from -1319 to -532kg. FRs of MeO-BDEs were >1, suggesting volatilization, although this is tentative due to uncertainties in their HLCs and binding to dissolved organic carbon.
19.	Bidleman, Terry F., et al. (author) Will Climate Change Influence Production and Environmental Pathways of Halogenated Natural Products? 2020 In: Environmental Science and Technology. - Washington, DC, USA : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 54:11, s. 6468-6485 Journal article (peer-reviewed)abstract Thousands of halogenated natural products (HNPs) pervade the terrestrial and marine environment. HNPs are generated by biotic and abiotic processes and range in complexity from low molecular mass natural halocarbons (nHCs, mostly halomethanes and haloethanes) to compounds of higher molecular mass which often contain oxygen and/or nitrogen atoms in addition to halogens (hHNPs). nHCs have a key role in regulating tropospheric and stratospheric ozone, while some hHNPs bioaccumulate and have toxic properties similar those of anthropogenic-persistent organic pollutants (POPs). Both chemical classes have common sources: biosynthesis by marine bacteria, phytoplankton, macroalgae, and some invertebrate animals, and both may be similarly impacted by alteration of production and transport pathways in a changing climate. The nHCs scientific community is advanced in investigating sources, atmospheric and oceanic transport, and forecasting climate change impacts through modeling. By contrast, these activities are nascent or nonexistent for hHNPs. The goals of this paper are to (1) review production, sources, distribution, and transport pathways of nHCs and hHNPs through water and air, pointing out areas of commonality, (2) by analogy to nHCs, argue that climate change may alter these factors for hHNPs, and (3) suggest steps to improve linkage between nHCs and hHNPs science to better understand and predict climate change impacts.
20.	Chartrand, Michelle, et al. (author) Compound specific isotope analysis of hexachlorocyclohexane isomers : a method for source fingerprinting and field investigation of in situ biodegradation 2015 In: Rapid Communications in Mass Spectrometry. - : John Wiley & Sons. - 0951-4198 .- 1097-0231. ; 29:6, s. 505-514 Journal article (peer-reviewed)abstract RATIONALE: The manufacturing and uses of hexachlorocyclohexane (HCH) have resulted in a serious environmentalchallenge and legacy. This study highlights the ability of compound specific isotope analysis (CSIA) to distinguishamong various HCH sources and to support the evaluation of the potential for in situ biodegradation in contaminatedgroundwater.METHODS: Tests were conducted to verify the absence of significant isotope fractionation during HCH sample preconcentrationincluding dichloromethane extraction, solvent exchange into iso-octane, and H2SO4 clean-up, and analysisby gas chromatography/combustion-isotope ratio mass spectrometry (GC/C-IRMS). The method was then applied tofour Technical Grade (TG) HCH mixtures procured from different sources and to groundwater samples from acontaminated site.RESULTS: The pre-concentration method enabled determination of carbon isotope ratios (δ13C values) of HCH isomerswith no significant isotopic fractionation. The TG-HCH mixtures had significantly different δ13C values. Moreover, forany given TG-HCH, all isomers had δ13C values within 1.1‰ of each other – a distinctly uniform fingerprint. At theHCH-contaminated field site, compared with source wells, downgradient wells showed significant (up to 5.1‰)enrichment in 13C and the δ13C values of the HCH isomers were significantly different from each other.CONCLUSIONS: A method was successfully developed for the CSIA of HCH isomers that showed potential for HCHsource differentiation and identification of HCH in situ biodegradation. At the HCH-contaminated site, the observedpreferential isotopic enrichment of certain isomers relative to others for a given source allows differentiation betweenbiodegraded and non-biodegraded HCH.
21.	Hites, Ronald, et al. (author) Atmospheric Concentrations of Hexachlorobenzene and Octachlorostyrene Are Uniform across the Great Lakes Region and Have Not Changed Much in 25 Years 2022 In: Environmental Science and Technology Letters. - : American Chemical Society (ACS). - 2328-8930. ; 9:8, s. 660-665 Journal article (peer-reviewed)abstract Hexachlorobenzene (HCB) was used in the United States from 1945 to 1966 as a fungicide on wheat, while octachlorostyrene (OCS) was never marketed. However, both HCB and OCS continue to be emitted into the atmosphere as byproducts of several industrial processes. We have measured the atmospheric concentrations of HCB and OCS in samples collected every 12 days at five sites on the shores of the North American Great Lakes since 1991. The geometric mean concentrations of HCB and OCS are ∼60 and 0.7 pg/m3, respectively, at all sites regardless of the local population, and these concentrations have not changed significantly over time. The concentrations of HCB measured here are similar to those reported by other studies of the northern troposphere and are ∼3 times those reported in the southern troposphere, suggesting that HCB sources are largely in the Northern Hemisphere. It is apparent that direct and recycled emissions of HCB and OCS into the northern troposphere are widespread in scope and, despite the elimination of HCB as a fungicide, have not changed in a meaningful way in the past 20–30 years. This is unlike the case for other legacy chemicals, for which global restrictions on their use have been more effective.
22.	Jantunen, Liisa, et al. (author) 20 Years of Air-Water Gas Exchange Observations for Pesticides in the Western Arctic Ocean 2015 In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 49:23, s. 13844-13852 Journal article (peer-reviewed)abstract The Arctic has been contaminated by legacy organochlorine pesticides (OCPs) and currently used pesticides (CUPs) through atmospheric transport and oceanic currents. Here we report the time trends and air−water exchange of OCPs and CUPs from research expeditions conducted between 1993 and 2013. Compounds determined in both air and water were trans- and cis-chlordanes (TC, CC), trans- and cis-nonachlors (TN, CN), heptachlor exo-epoxide (HEPX), dieldrin (DIEL), chlorobornanes (ΣCHBs and toxaphene), dacthal (DAC), endosulfans and metabolite endosulfan sulfate (ENDO-I, ENDO-II, and ENDO SUL), chlorothalonil (CHT), chlorpyrifos (CPF), and trifluralin (TFN). Pentachloronitrobenzene (PCNB and quintozene) and its soil metabolite pentachlorothianisole (PCTA) were also found in air. Concentrations of most OCPs declined in surface water, whereas some CUPs increased (ENDO-I, CHT, and TFN) or showed no significant change (CPF and DAC), and most compounds declined in air. Chlordane compound fractions TC/(TC + CC) and TC/(TC + CC + TN) decreased in water and air, while CC/(TC + CC + TN) increased. TN/(TC + CC + TN) also increased in air and slightly, but not significantly, in water. These changes suggest selective removal of more labile TC and/or a shift in chlordane sources. Water−air fugacity ratios indicated net volatilization (FR > 1.0) or near equilibrium (FR not significantly different from 1.0) for most OCPs but net deposition (FR < 1.0) for ΣCHBs. Net deposition was shown for ENDO-I on all expeditions, while the net exchange direction of other CUPs varied. Understanding the processes and current state of air−surface exchange helps to interpret environmental exposure and evaluate the effectiveness of international protocols and provides insights for the environmental fate of new and emerging chemicals.
23.	Kupryianchyk, Darya, et al. (author) Industrial and natural compounds in filter-feeding black fly larvae and water in 3 tundra streams 2018 In: Environmental Toxicology and Chemistry. - : John Wiley & Sons. - 0730-7268 .- 1552-8618. ; 37:12, s. 3011-3017 Journal article (peer-reviewed)abstract We report concentrations of polychlorinated biphenyls, polybrominated diphenyl ethers, novel flame retardants, and naturally occurring bromoanisoles in water and filter-feeding black fly (Simuliidae) larvae in 3 tundra streams in northern Sweden. The results demonstrate that black fly larvae accumulate a wide range of organic contaminants and can be used as bioindicators of water pollution in Arctic streams.
24.	Kurt-Karakus, Perihan Binnur, et al. (author) CURRENT-USE PESTICIDES IN INLAND LAKE WATERS, PRECIPITATION, AND AIR FROM ONTARIO, CANADA 2011 In: Environmental Toxicology and Chemistry. - : WILEY-BLACKWELL. - 0730-7268 .- 1552-8618. ; 30:7, s. 1539-1548 Journal article (peer-reviewed)abstract Concentrations of current-use pesticides (CUPs) in water, zooplankton, precipitation, and air samples as well as stereoisomer fractions (SF; herbicidally active/total stereoisomers) of metolachlor were determined in water samples collected from 10 remote inland lakes in Ontario, Canada, between 2003 and 2005. The most frequently detected chemicals in lake water, precipitation, and air were alpha-endosulfan, atrazine, metolachlor, chlorpyrifos, chlorothalonil, and trifluralin, and alpha-endosulfan and chlorpyrifos were the chemicals detected frequently in zooplankton. Air concentrations of these CUPs were within the range of previously reported values for background sites in the Great Lakes basin. High detection frequency of CUPs in lake water and precipitation was attributed to high usage amounts, but some CUPs such as ametryn and disulfoton that were not used in Ontario were also detected. Mean bioaccumulation factors (wet wt) in zooplankton for endosulfan ranged from 160 to 590 and from 20 to 60 for chlorpyrifos. The overall median SF of metolachlor in precipitation samples (0.846) was similar to that of the commercial S-metolaehlor (0.882). However, the median SF of metolachlor in water from all sampled inland lakes (0.806) was significantly lower compared with Ontario rivers (0.873) but higher compared with previous measurements in the Great Lakes (0.710). Lakes with smaller watershed areas showed higher SFs, supporting the hypothesis of stereoselective processing of deposited metolachlor within the watersheds, followed by transport to the lakes. Environ. Toxicol. Chem. 2011;30:1539-1548. (C) 2011 SETAC
25.	Lohmann, Rainer, et al. (author) Passive-sampler-derived PCB and OCP concentrations in the waters of the world : first results from the AQUA-GAPS/MONET network 2023 In: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 57:25, s. 9342-9352 Journal article (peer-reviewed)abstract Persistent organic pollutants (POPs) are recognized as pollutants of global concern, but so far, information on the trends of legacy POPs in the waters of the world has been missing due to logistical, analytical, and financial reasons. Passive samplers have emerged as an attractive alternative to active water sampling methods as they accumulate POPs, represent time-weighted average concentrations, and can easily be shipped and deployed. As part of the AQUA-GAPS/MONET, passive samplers were deployed at 40 globally distributed sites between 2016 and 2020, for a total of 21 freshwater and 40 marine deployments. Results from silicone passive samplers showed α-hexachlorocyclohexane (HCH) and γ-HCH displaying the greatest concentrations in the northern latitudes/Arctic Ocean, in stark contrast to the more persistent penta (PeCB)- and hexachlorobenzene (HCB), which approached equilibrium across sampling sites. Geospatial patterns of polychlorinated biphenyl (PCB) aqueous concentrations closely matched original estimates of production and use, implying limited global transport. Positive correlations between log-transformed concentrations of Σ7PCB, ΣDDTs, Σendosulfan, and Σchlordane, but not ΣHCH, and the log of population density (p < 0.05) within 5 and 10 km of the sampling sites also supported limited transport from used sites. These results help to understand the extent of global distribution, and eventually time-trends, of organic pollutants in aquatic systems, such as across freshwaters and oceans. Future deployments will aim to establish time-trends at selected sites while adding to the geographical coverage.

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