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HBCDs in the top predator Greenland shark (Somniosus microcephalus) from Greenla...
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Occurrence of PBDEs in the Greenland Shark Somniosus microcephalus
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Age of black dogfish ( Centroscyllium fabricii ) estimated from fin spines growt...
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Characteristics And Propagation Of Airgun Pulses In Shallow Water With Implicati...
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Air-sea fluxes of water vapour and CO 2 in the North Atlantic
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Characteristics and propagation of airgun pulses in shallow water with implicati...
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Timing and genesis of base- metal mineralisation in black shales of the Upper Pe...
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The importance of genetic verification for determination of Atlantic salmon in n...
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Gm Types of Greenland Eskimos
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Age of black dogfish (Centroscyllium fabricii) estimated from fin spines growth...
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Thermochemical sulfate reduction by hydrocarbons in an evaporate-carbonate reser...
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How a simple adaptive foraging strategy can lead to emergent home ranges and inc...
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Foraging behaviour and fuel accumulation of capital breeders during spring migra...
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Genetic variation in Norwegian piscine myocarditis virus in Atlantic salmon, Sal...
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Allee effect in polar bears: a potential consequence of polychlorinated biphenyl...
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Competition between whiting and cod in the western Baltic Sea ...
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Competition between whiting and cod in the western Baltic Sea ...
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Evidence of DDTs in the Greenland shark Somniosus microcephalus from Greenland s...
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A Fast Light-weight Core Drill
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Allee effect in polar bears: A potential consequence of polychlorinated biphenyl...
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