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Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways.

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Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways. / Macdonald, R. W.; Barrie, L. A.; Bidleman, T. F. et al.
In: Science of the Total Environment, Vol. 254, No. 2-3, 01.06.2000, p. 93-234.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Macdonald, RW, Barrie, LA, Bidleman, TF, Diamond, ML, Gregor, DJ, Semkin, RG, Strachan, WMJ, Li, YFWF, Alaee, M, Alexeeva, LB, Backus, SM, Bailey, RE, Bewers, JM, Gobeil, C, Halsall, CJ, Harner, T, Hoff, JT, Jantunen, LMM, Lockhart, WL, Mackay, D, Muir, DCG, Pudykiewicz, J, Reimer, KJ, Smith, JN, Stern, GA, Schroeder, WH, Wagemann, R & Yunker, MB 2000, 'Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways.', Science of the Total Environment, vol. 254, no. 2-3, pp. 93-234. https://doi.org/10.1016/S0048-9697(00)00434-4

APA

Macdonald, R. W., Barrie, L. A., Bidleman, T. F., Diamond, M. L., Gregor, D. J., Semkin, R. G., Strachan, W. M. J., Li, Y. F. W. F., Alaee, M., Alexeeva, L. B., Backus, S. M., Bailey, R. E., Bewers, J. M., Gobeil, C., Halsall, C. J., Harner, T., Hoff, J. T., Jantunen, L. M. M., Lockhart, W. L., ... Yunker, M. B. (2000). Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways. Science of the Total Environment, 254(2-3), 93-234. https://doi.org/10.1016/S0048-9697(00)00434-4

Vancouver

Macdonald RW, Barrie LA, Bidleman TF, Diamond ML, Gregor DJ, Semkin RG et al. Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways. Science of the Total Environment. 2000 Jun 1;254(2-3):93-234. doi: 10.1016/S0048-9697(00)00434-4

Author

Macdonald, R. W. ; Barrie, L. A. ; Bidleman, T. F. et al. / Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways. In: Science of the Total Environment. 2000 ; Vol. 254, No. 2-3. pp. 93-234.

Bibtex

@article{c2d347756c304b7b98997d5078bd7ad0,
title = "Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways.",
abstract = "Recent studies of contaminants under the Canadian Northern Contaminants Program (NCP) have substantially enhanced our understanding of the pathways by which contaminants enter Canada{\textquoteright}s Arctic and move through terrestrial and marine ecosystems there. Building on a previous review (Barrie et al., Arctic contaminants: sources, occurrence and pathways. Sci Total Environ 1992:1–74), we highlight new knowledge developed under the NCP on the sources, occurrence and pathways of contaminants (organochlorines, Hg, Pb and Cd, PAHs, artificial radionuclides). Starting from the global scale, we examine emission histories and sources for selected contaminants focussing especially on the organochlorines. Physical and chemical properties, transport processes in the environment (e.g. winds, currents, partitioning), and models are then used to identify, understand and illustrate the connection between the contaminant sources in industrial and agricultural regions to the south and the eventual arrival of contaminants in remote regions of the Arctic. Within the Arctic, we examine how contaminants impinge on marine and terrestrial pathways and how they are subsequently either removed to sinks or remain where they can enter the biosphere. As a way to focus this synthesis on key concerns of northern residents, a number of special topics are examined including: a mass balance for HCH and toxaphene (CHBs) in the Arctic Ocean; a comparison of PCB sources within Canada{\textquoteright}s Arctic (Dew Line Sites) with PCBs imported through long-range transport; an evaluation of concerns posed by three priority metals — Hg, Pb and Cd; an evaluation of the risks from artificial radionuclides in the ocean; a review of what is known about new-generation pesticides that are replacing the organochlorines; and a comparison of natural vs. anthropogenic sources of PAH in the Arctic. The reseArch and syntheses provide compelling evidence for close connectivity between the global emission of contaminants from industrial and agricultural activities and the Arctic. For semi-volatile compounds that partition strongly into cold water (e.g. HCH) we have seen an inevitable loading of Arctic aquatic reservoirs. Drastic HCH emission reductions have been rapidly followed by reduced atmospheric burdens with the result that the major reservoir and transport agent has become the ocean. In the Arctic, it will take decades for the upper ocean to clear itself of HCH. For compounds that partition strongly onto particles, and for which the soil reservoir is most important (e.g. PCBs), we have seen a delay in their arrival in the Arctic and some fractionation toward more volatile compounds (e.g. lower-chlorinated PCBs). Despite banning the production of PCB in the 1970s, and despite decreases of PCBs in environmental compartments in temperate regions, the Arctic presently shows little evidence of reduced PCB loadings. We anticipate a delay in PCB reductions in the Arctic and environmental lifetimes measured in decades. Although artificial radionuclides have caused great concern due to their direct disposal on Russian Shelves, they are found to pose little threat to Canadian waters and, indeed, much of the radionuclide inventory can be explained as remnant global fallout, which was sharply curtailed in the 1960s, and waste emissions released under license by the European reprocessing plants. Although Cd poses a human dietary concern both for terrestrial and marine mammals, we find little evidence that Cd in marine systems has been impacted by human activities. There is evidence of contaminant Pb in the Arctic, but loadings appear presently to be decreasing due to source controls (e.g. removal of Pb from gasoline) in Europe and North America. Of the metals, Hg provokes the greatest concern; loadings appear to be increasing in the Arctic due to global human activities, but such loadings are not evenly distributed nor are the pathways by which they enter and move within the Arctic well understood.",
keywords = "Canadian Arctic, Chemical contaminants, Metals, Model, Organochlorine, Polycyclic aromatic hydrocarbons, Pathways, Radionuclides, Temporal trends",
author = "Macdonald, {R. W.} and Barrie, {L. A.} and Bidleman, {T. F.} and Diamond, {M. L.} and Gregor, {D. J.} and Semkin, {R. G.} and Strachan, {W. M. J.} and Li, {Y. F. W. F.} and M. Alaee and Alexeeva, {L. B.} and Backus, {S. M.} and Bailey, {R. E.} and Bewers, {J. M.} and C. Gobeil and Halsall, {Crispin J.} and T. Harner and Hoff, {J. T.} and Jantunen, {L. M. M.} and Lockhart, {W. L.} and D. Mackay and Muir, {D. C. G.} and J. Pudykiewicz and Reimer, {K. J.} and Smith, {J. N.} and Stern, {G. A.} and Schroeder, {W. H.} and R. Wagemann and Yunker, {M. B.}",
year = "2000",
month = jun,
day = "1",
doi = "10.1016/S0048-9697(00)00434-4",
language = "English",
volume = "254",
pages = "93--234",
journal = "Science of the Total Environment",
issn = "0048-9697",
publisher = "Elsevier Science B.V.",
number = "2-3",

}

RIS

TY - JOUR

T1 - Contaminants in the Canadian Arctic : 5 years of progress in understanding sources, occurrence and pathways.

AU - Macdonald, R. W.

AU - Barrie, L. A.

AU - Bidleman, T. F.

AU - Diamond, M. L.

AU - Gregor, D. J.

AU - Semkin, R. G.

AU - Strachan, W. M. J.

AU - Li, Y. F. W. F.

AU - Alaee, M.

AU - Alexeeva, L. B.

AU - Backus, S. M.

AU - Bailey, R. E.

AU - Bewers, J. M.

AU - Gobeil, C.

AU - Halsall, Crispin J.

AU - Harner, T.

AU - Hoff, J. T.

AU - Jantunen, L. M. M.

AU - Lockhart, W. L.

AU - Mackay, D.

AU - Muir, D. C. G.

AU - Pudykiewicz, J.

AU - Reimer, K. J.

AU - Smith, J. N.

AU - Stern, G. A.

AU - Schroeder, W. H.

AU - Wagemann, R.

AU - Yunker, M. B.

PY - 2000/6/1

Y1 - 2000/6/1

N2 - Recent studies of contaminants under the Canadian Northern Contaminants Program (NCP) have substantially enhanced our understanding of the pathways by which contaminants enter Canada’s Arctic and move through terrestrial and marine ecosystems there. Building on a previous review (Barrie et al., Arctic contaminants: sources, occurrence and pathways. Sci Total Environ 1992:1–74), we highlight new knowledge developed under the NCP on the sources, occurrence and pathways of contaminants (organochlorines, Hg, Pb and Cd, PAHs, artificial radionuclides). Starting from the global scale, we examine emission histories and sources for selected contaminants focussing especially on the organochlorines. Physical and chemical properties, transport processes in the environment (e.g. winds, currents, partitioning), and models are then used to identify, understand and illustrate the connection between the contaminant sources in industrial and agricultural regions to the south and the eventual arrival of contaminants in remote regions of the Arctic. Within the Arctic, we examine how contaminants impinge on marine and terrestrial pathways and how they are subsequently either removed to sinks or remain where they can enter the biosphere. As a way to focus this synthesis on key concerns of northern residents, a number of special topics are examined including: a mass balance for HCH and toxaphene (CHBs) in the Arctic Ocean; a comparison of PCB sources within Canada’s Arctic (Dew Line Sites) with PCBs imported through long-range transport; an evaluation of concerns posed by three priority metals — Hg, Pb and Cd; an evaluation of the risks from artificial radionuclides in the ocean; a review of what is known about new-generation pesticides that are replacing the organochlorines; and a comparison of natural vs. anthropogenic sources of PAH in the Arctic. The reseArch and syntheses provide compelling evidence for close connectivity between the global emission of contaminants from industrial and agricultural activities and the Arctic. For semi-volatile compounds that partition strongly into cold water (e.g. HCH) we have seen an inevitable loading of Arctic aquatic reservoirs. Drastic HCH emission reductions have been rapidly followed by reduced atmospheric burdens with the result that the major reservoir and transport agent has become the ocean. In the Arctic, it will take decades for the upper ocean to clear itself of HCH. For compounds that partition strongly onto particles, and for which the soil reservoir is most important (e.g. PCBs), we have seen a delay in their arrival in the Arctic and some fractionation toward more volatile compounds (e.g. lower-chlorinated PCBs). Despite banning the production of PCB in the 1970s, and despite decreases of PCBs in environmental compartments in temperate regions, the Arctic presently shows little evidence of reduced PCB loadings. We anticipate a delay in PCB reductions in the Arctic and environmental lifetimes measured in decades. Although artificial radionuclides have caused great concern due to their direct disposal on Russian Shelves, they are found to pose little threat to Canadian waters and, indeed, much of the radionuclide inventory can be explained as remnant global fallout, which was sharply curtailed in the 1960s, and waste emissions released under license by the European reprocessing plants. Although Cd poses a human dietary concern both for terrestrial and marine mammals, we find little evidence that Cd in marine systems has been impacted by human activities. There is evidence of contaminant Pb in the Arctic, but loadings appear presently to be decreasing due to source controls (e.g. removal of Pb from gasoline) in Europe and North America. Of the metals, Hg provokes the greatest concern; loadings appear to be increasing in the Arctic due to global human activities, but such loadings are not evenly distributed nor are the pathways by which they enter and move within the Arctic well understood.

AB - Recent studies of contaminants under the Canadian Northern Contaminants Program (NCP) have substantially enhanced our understanding of the pathways by which contaminants enter Canada’s Arctic and move through terrestrial and marine ecosystems there. Building on a previous review (Barrie et al., Arctic contaminants: sources, occurrence and pathways. Sci Total Environ 1992:1–74), we highlight new knowledge developed under the NCP on the sources, occurrence and pathways of contaminants (organochlorines, Hg, Pb and Cd, PAHs, artificial radionuclides). Starting from the global scale, we examine emission histories and sources for selected contaminants focussing especially on the organochlorines. Physical and chemical properties, transport processes in the environment (e.g. winds, currents, partitioning), and models are then used to identify, understand and illustrate the connection between the contaminant sources in industrial and agricultural regions to the south and the eventual arrival of contaminants in remote regions of the Arctic. Within the Arctic, we examine how contaminants impinge on marine and terrestrial pathways and how they are subsequently either removed to sinks or remain where they can enter the biosphere. As a way to focus this synthesis on key concerns of northern residents, a number of special topics are examined including: a mass balance for HCH and toxaphene (CHBs) in the Arctic Ocean; a comparison of PCB sources within Canada’s Arctic (Dew Line Sites) with PCBs imported through long-range transport; an evaluation of concerns posed by three priority metals — Hg, Pb and Cd; an evaluation of the risks from artificial radionuclides in the ocean; a review of what is known about new-generation pesticides that are replacing the organochlorines; and a comparison of natural vs. anthropogenic sources of PAH in the Arctic. The reseArch and syntheses provide compelling evidence for close connectivity between the global emission of contaminants from industrial and agricultural activities and the Arctic. For semi-volatile compounds that partition strongly into cold water (e.g. HCH) we have seen an inevitable loading of Arctic aquatic reservoirs. Drastic HCH emission reductions have been rapidly followed by reduced atmospheric burdens with the result that the major reservoir and transport agent has become the ocean. In the Arctic, it will take decades for the upper ocean to clear itself of HCH. For compounds that partition strongly onto particles, and for which the soil reservoir is most important (e.g. PCBs), we have seen a delay in their arrival in the Arctic and some fractionation toward more volatile compounds (e.g. lower-chlorinated PCBs). Despite banning the production of PCB in the 1970s, and despite decreases of PCBs in environmental compartments in temperate regions, the Arctic presently shows little evidence of reduced PCB loadings. We anticipate a delay in PCB reductions in the Arctic and environmental lifetimes measured in decades. Although artificial radionuclides have caused great concern due to their direct disposal on Russian Shelves, they are found to pose little threat to Canadian waters and, indeed, much of the radionuclide inventory can be explained as remnant global fallout, which was sharply curtailed in the 1960s, and waste emissions released under license by the European reprocessing plants. Although Cd poses a human dietary concern both for terrestrial and marine mammals, we find little evidence that Cd in marine systems has been impacted by human activities. There is evidence of contaminant Pb in the Arctic, but loadings appear presently to be decreasing due to source controls (e.g. removal of Pb from gasoline) in Europe and North America. Of the metals, Hg provokes the greatest concern; loadings appear to be increasing in the Arctic due to global human activities, but such loadings are not evenly distributed nor are the pathways by which they enter and move within the Arctic well understood.

KW - Canadian Arctic

KW - Chemical contaminants

KW - Metals

KW - Model

KW - Organochlorine

KW - Polycyclic aromatic hydrocarbons

KW - Pathways

KW - Radionuclides

KW - Temporal trends

U2 - 10.1016/S0048-9697(00)00434-4

DO - 10.1016/S0048-9697(00)00434-4

M3 - Journal article

VL - 254

SP - 93

EP - 234

JO - Science of the Total Environment

JF - Science of the Total Environment

SN - 0048-9697

IS - 2-3

ER -