The concentration and isotopic composition of U dissolved in pore waters from hemipelagic sediments of the Labrador Sea were determined by thermal ionization mass spectrometry in two 30 cm long box cores. The present fluxes of seawater U that diffuses across the sediment–seawater interface are on the order of 2–4 μg/(cm2∙ka). This diffusion imposes decreasing gradients of dissolved U downwards, but the U concentration in pore waters immediately below the surface is much lower than that of open-ocean seawater. This is a primary feature that cannot be explained by carbonate precipitation due to decompression during core retrieval. More likely, it reflects the presence of a stagnant benthic boundary layer above the sediment–water interface, in which molecular diffusion of U is slower than in the overlying turbulently mixed seawater, and (or) of microzones near the interface where U is bioaccumulated. Uranium is adsorbed at depths onto the solid phase in response to changes in the redox conditions within the sediments. In the Labrador Sea, this occurs at the onset of iron reduction and corresponds to a colour transition from brown to grey. Adsorption of U is sufficiently large to alter the initial content and the isotopic composition of U in the detrital component. Accumulation of authigenic U on the solid phase does not proceed at a steady state. This is due to the uneven burial rates of organic matter, which is essential to the establishment of redox conditions appropriate for U reduction, and concomitant stepwise displacement of the redox fronts. This indicates that discrete periods of enhanced primary productivity recurred over the last millenium in the Labrador Sea, inducing U fluxes to the sediments greater than they are now. Measured pore-water U concentrations are greater than the overlying seawater at depth in the cores, despite the fact that none of the conditions necessary to release U under reducing conditions are present in the sediments. More likely, U-bearing particles < 0.45 μm were transferred with the solution phase through the filtering device, artificially increasing the pore-water U content.