1. |
- Carlsson, Pernilla, et al.
(författare)
-
Polychlorinated biphenyls (PCBs) as sentinels for the elucidation of Arctic environmental change processes : a comprehensive review combined with ArcRisk project results
- 2018
-
Ingår i: Environmental Science and Pollution Research. - : Springer Science and Business Media LLC. - 0944-1344 .- 1614-7499. ; 25:23, s. 22499-22528
-
Forskningsöversikt (refereegranskat)abstract
- Polychlorinated biphenyls (PCBs) can be used as chemical sentinels for the assessment of anthropogenic influences on Arctic environmental change. We present an overview of studies on PCBs in the Arctic and combine these with the findings from ArcRisk-a major European Union-funded project aimed at examining the effects of climate change on the transport of contaminants to and their behaviour of in the Arctic-to provide a case study on the behaviour and impact of PCBs over time in the Arctic. PCBs in the Arctic have shown declining trends in the environment over the last few decades. Atmospheric long-range transport from secondary and primary sources is the major input of PCBs to the Arctic region. Modelling of the atmospheric PCB composition and behaviour showed some increases in environmental concentrations in a warmer Arctic, but the general decline in PCB levels is still the most prominent feature. 'Within-Arctic' processing of PCBs will be affected by climate change-related processes such as changing wet deposition. These in turn will influence biological exposure and uptake of PCBs. The pan-Arctic rivers draining large Arctic/sub-Arctic catchments provide a significant source of PCBs to the Arctic Ocean, although changes in hydrology/sediment transport combined with a changing marine environment remain areas of uncertainty with regard to PCB fate. Indirect effects of climate change on human exposure, such as a changing diet will influence and possibly reduce PCB exposure for indigenous peoples. Body burdens of PCBs have declined since the 1980s and are predicted to decline further.
|
|
2. |
- Degrendele, Celine, et al.
(författare)
-
Multiyear levels of PCDD/Fs, dl-PCBs and PAHs in background air in central Europe and implications for deposition
- 2020
-
Ingår i: Chemosphere. - : Elsevier. - 0045-6535 .- 1879-1298. ; 240
-
Tidskriftsartikel (refereegranskat)abstract
- This study presents four years ambient monitoring data of seventeen 2,3,7,8-chlorine substituted poly-chlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs), twelve dioxin-like poly-chlorinated biphenyls (dl-PCBs) and sixteen polycyclic aromatic hydrocarbons (PAHs) designed by the US EPA at a background site in central Europe during 2011-2014. The concentrations expressed as toxic equivalents (TEQs) using the WHO2005-scheme for PCDD/Fs (0.2 fg m(-3)-61.1 fg m(-3)) were higher than for dl-PCBs (0.01 fg m(-3)-2.9 fg m(-3)), while the opposite was found in terms of mass concentrations. Sigma PAHs ranged from 0.20 ng m(-3) to 134 ng(-3). The mass concentration profile of PCDD/Fs, dl-PCBs and PAHs was similar throughout the four years. PCDD/Fs and PAHs concentrations were dominated by primary sources peaking in winter, while those of dl-PCBs were controlled by secondary sources characterized by a spring-summer peak. During 2011-2014, no significant decrease in the atmospheric levels of Sigma PCDD/Fs was observed. On the other hand, the concentrations of Sigma dl-PCBs and Sigma PAHs were decreasing, with halving times of 5.7 and 2.7 years, respectively. We estimated that 422 pg m(-2) year pg m(-2) year TEQ PCDD/Fs and 3.48 pg m(-2) year(-1)-15.8 pg m(-2) year(-1) TEQ dl-PCBs were transferred from the air to the ground surfaces via dry particulate deposition during 2011-2014.
|
|
3. |
|
|
4. |
- Kukucka, Petr, 1982-, et al.
(författare)
-
Contamination of Antarctic snow by polycyclic aromatic hydrocarbons dominated by combustion sources in the polar region
- 2010
-
Ingår i: Environmental Chemistry. - : CSIRO Publishing. - 1448-2517 .- 1449-8979. ; 7:6, s. 504-513
-
Tidskriftsartikel (refereegranskat)abstract
- Firn samples attributed to the period between 2002 and 2005 were collected from a snow pit on the Ekstrom Shelf Ice in the Weddell Sea (70 degrees 43.8'S, 8 degrees 25.1'W). Low-volume meltwater samples (5 mL) were extracted by solid-phase microextraction (SPME) and analysed for polycyclic aromatic hydrocarbons (PAHs) by gas chromatography-mass spectrometry. The recovery of the analytical method for the 4-6 ring PAHs was low. PAH concentrations in snow were found within the range of 26-197 ng L(-1). The most prevailing substances were determined to be naphthalene, 1- and 2-methylnaphthalene, acenaphthylene, acenaphthene and phenanthrene, with naphthalene accounting for an overall mean of 82% of total PAH. Potential emission sources of PAHs in snow were studied using back-trajectory statistics and available emission data of combustion sources in and around Antarctica. The distance to the sources (ships and research stations) in this region was found to control the snow PAH concentrations. There was no indication for intercontinental transport or marine sources.
|
|
5. |
- Lammel, Gerhard, et al.
(författare)
-
Air and seawater pollution and air-sea gas exchange of persistent toxic substances in the Aegean Sea : spatial trends of PAHs, PCBs, OCPs and PBDEs
- 2015
-
Ingår i: Environmental Science and Pollution Research. - : Springer Berlin/Heidelberg. - 0944-1344 .- 1614-7499. ; 22:15, s. 11301-11313
-
Tidskriftsartikel (refereegranskat)abstract
- Near-ground air (26 substances) and surface seawater (55 substances) concentrations of persistent toxic substances (PTS) were determined in July 2012 in a coordinated and coherent way around the Aegean Sea based on passive air (10 sites in 5 areas) and water (4 sites in 2 areas) sampling. The direction of air-sea exchange was determined for 18 PTS. Identical samplers were deployed at all sites and were analysed at one laboratory. hexachlorobenzene (HCB), hexachlorocyclohexanes (HCHs) as well as dichlorodiphenyltrichloroethane (DDT) and its degradation products are evenly distributed in the air of the whole region. Air concentrations of p,p'-dichlorodiphenyldichloroethylene (p,p'-DDE) and o,p'-DDT and seawater concentrations of p,p'-DDE and p,p'-DDD were elevated in Thermaikos Gulf, northwestern Aegean Sea. The polychlorinated biphenyl (PCB) congener pattern in air is identical throughout the region, while polybrominated diphenylether (PBDE)patterns are obviously dissimilar between Greece and Turkey. Various pollutants, polycyclic aromatic hydrocarbons (PAHs), PCBs, DDE, and penta- and hexachlorobenzene are found close to phase equilibrium or net-volatilisational (upward flux), similarly at a remote site (on Crete) and in the more polluted Thermaikos Gulf. The results suggest that effective passive air sampling volumes may not be representative across sites when PAHs significantly partitioning to the particulate phase are included.
|
|
6. |
- Lammel, Gerhard, et al.
(författare)
-
Organochlorine pesticides and polychlorinated biphenyls along an east-to-west gradient in subtropical North Atlantic surface water
- 2017
-
Ingår i: Environmental Science and Pollution Research. - Hedielberg, Germany : Springer. - 0944-1344 .- 1614-7499. ; 24:12, s. 11045-11052
-
Tidskriftsartikel (refereegranskat)abstract
- Despite the fact that most persistent toxic substances have hardly been primarily emitted for several decades, their concentrations are only slowly decreasing in the global oceans. Surface seawater samples were collected along a 38°-24° N/28°-67° W transect in the subtropical North Atlantic Ocean. While the concentration levels of hexachlorobenzene (2.1-6.1 pg L(-1)), dichlorodiphenyltrichloroethane (DDT, up to 2.1 pg L(-1)) and polychlorinated biphenyls (PCB, 10.8-24.9 pg L(-1)) were in the same range as observed earlier in the North Atlantic, hexachlorocyclohexane (HCH, 90-627 pg L(-1)) was found elevated, partly also relative to previous measurements in the same sea region. Hereby, the ratio α-HCH/γ-HCH was very low, 0.09-0.13. Chlordane and endosulfan were found in the range <3.0-11.1 and <5.8-8.8 pg L(-1) respectively. DDT metabolites, endrin and related pesticides were found below quantification limits. Spatial pollution patterns in surface seawaters seem to be determined by atmospheric and oceanic transport patterns, rather than by mixing and air-sea equilibrium. The comparison with global multicompartment chemistry-transport model predictions of surface seawater levels indicate underestimated degradation of PCBs and overestimated emissions of endosulfan.
|
|
7. |
- Mayer, Ludovic, et al.
(författare)
-
Widespread Pesticide Distribution in the European Atmosphere Questions their Degradability in Air
- 2024
-
Ingår i: Environmental Science and Technology. - 0013-936X. ; 58:7, s. 3342-3352
-
Tidskriftsartikel (refereegranskat)abstract
- Risk assessment of pesticide impacts on remote ecosystems makes use of model-estimated degradation in air. Recent studies suggest these degradation rates to be overestimated, questioning current pesticide regulation. Here, we investigated the concentrations of 76 pesticides in Europe at 29 rural, coastal, mountain, and polar sites during the agricultural application season. Overall, 58 pesticides were observed in the European atmosphere. Low spatial variation of 7 pesticides suggests continental-scale atmospheric dispersal. Based on concentrations in free tropospheric air and at Arctic sites, 22 pesticides were identified to be prone to long-range atmospheric transport, which included 15 substances approved for agricultural use in Europe and 7 banned ones. Comparison between concentrations at remote sites and those found at pesticide source areas suggests long atmospheric lifetimes of atrazine, cyprodinil, spiroxamine, tebuconazole, terbuthylazine, and thiacloprid. In general, our findings suggest that atmospheric transport and persistence of pesticides have been underestimated and that their risk assessment needs to be improved.
|
|
8. |
- Mulder, Marie D., et al.
(författare)
-
Long-range atmospheric transport of PAHs, PCBs and PBDEs to the central and eastern Mediterranean and changes of PCB and PBDE congener patterns in summer 2010
- 2015
-
Ingår i: Atmospheric Environment. - : Elsevier. - 1352-2310 .- 1873-2844. ; 111, s. 51-59
-
Tidskriftsartikel (refereegranskat)abstract
- The central and eastern Mediterranean is a receptor area for persistent organic pollutants (POPs) emitted in western, central and eastern Europe, particularly during summer. Atmospheric concentrations of PCBs, DDXs, PBDEs, penta- and hexachlorobenzene were measured during a ship-borne survey in the summer of 2010. The concentration of PCBs (sum of 7 congeners) was 3.61 (2.08-7.72) pg m(-3), of which 6.7% was associated with the particulate phase. The mean concentration of DDT isoi-ners and their metabolites, DDE and DDD, was 2.60 (0.46-7.60) pg m(-3) (particulate mass fraction theta = 0.097), of penta- and hexachlorobenzene 0.22 (<039-2.80) pg m(-3) and 6.29 (2.48-24.16) pg m(-3), respectively, and of PBDEs (sum of 8 congeners) 7.31 (2.80-19.89) pg m(-3). The air masses studied had been transported mostly across central Europe, some crossing western Europe. The observed changes of PCB congener patterns along transport routes are in agreement with the perception that the reaction with the OH radical is dominating PCB atmospheric lifetime, and indicate an overestimation of the second order gas-phase reaction rate coefficient of PCB:153 with OH by structure-activity relationship.
|
|
9. |
- Mulder, Marie D., et al.
(författare)
-
Reprint of : Long-range atmospheric transport of PAHs, PCBs and PBDEs to the central and eastern Mediterranean and changes of PCB and PBDE congener patterns in summer 2010 (Reprinted from Atmospheric Environment, vol 111, pg 51-59)
- 2015
-
Ingår i: Atmospheric Environment. - : Elsevier. - 1352-2310 .- 1873-2844. ; 121, s. 66-74
-
Tidskriftsartikel (refereegranskat)abstract
- The central and eastern Mediterranean is a receptor area for persistent organic pollutants (POPs) emitted in western, central and eastern Europe, particularly during summer. Atmospheric concentrations of PCBs, DDXs, PBDEs, penta- and hexachlorobenzene were measured during a ship-borne survey in the summer of 2010. The concentration of PCBs (sum of 7 congeners) was 3.61 (2.08-7.72) pg m(-3), of which 6.7% was associated with the particulate phase. The mean concentration of DDT isomers and their metabolites, DDE and DDD, was 2.60 (0.46-7.60) pg m(-3) (particulate mass fraction theta = 0.097), of penta- and hexachlorobenzene 0.22 (<0.39-2.80) pg m(-3) and 6.29(2.48-24.16) pg m(-3), respectively, and of PBDEs (sum of 8 congeners) 7.31 (2.80-19.89) pg m(-3). The air masses studied had been transported mostly across central Europe, some crossing western Europe. The observed changes of PCB congener patterns along transport routes are in agreement with the perception that the reaction with the OH radical is dominating PCB atmospheric lifetime, and indicate an overestimation of the second order gas-phase reaction rate coefficient of PCB153 with OH by structure-activity relationship.
|
|