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Limnological regime shifts caused by climate warming and Lesser Snow Goose popul...
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Aqueous uptake and sublethal toxicity of p,p′-DDE in non-feeding larval stages o...
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Tithonian mafic intrusions in north-central Newfoundland: link to Atlantic rifti...
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Did enhanced afforestation cause high severity peat burn in the Fort McMurray Ho...
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Environmental DNA dispersal from Atlantic salmon farms
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Biological and geochemical changes in shallow lakes of the Hudson Bay Lowlands:...
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Re-evaluating the dietary requirement of EPA and DHA for Atlantic salmon in fres...
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The sedimentary and crustal velocity structure of Makarov Basin and adjacent Alp...
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The Eoarchean legacy of Isua (Greenland) worth preserving for future generations
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Net atmospheric mercury deposition to Svalbard: Estimates from lacustrine sedime...
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Solar Radiation and Air and Ground Temperature Relations in the Cold and Hyper‐A...
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Triassic echinoids (Echinodermata) from the Aksala Formation, north Lake Laberge...
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Evaluation of carbon dioxide sequestration via interaction with peridotite and p...
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Uncertainty-Incorporated Ice and Open Water Detection on Dual-Polarized SAR Sea...
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The combined effects of predation, fishing, and ocean productivity on salmon spe...
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The Impact of Low Flow on Riverine Food Webs in South-Central Newfoundland
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Fractionation of hydrogen and oxygen in artificial sea ice with corrections for...
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Multifrequency Microwave Backscatter From a Highly Saline Snow Cover on Smooth F...
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Dietary characteristics of co-occurring polar cod (Boreogadus saida) and capelin...
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Diurnal Scale Controls on C-Band Microwave Backscatter From Snow-Covered First-Y...
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