Abstract. Exchange of dissolved substances at the sediment–water
interface provides an important link between the short-term and long-term
geochemical cycles in the ocean. A second, as yet poorly understood
sediment–water exchange is supported by low-temperature circulation of
seawater through the oceanic basement underneath the sediments. From the
basement, upwards diffusing oxygen and other dissolved species modify the
sediment, whereas reaction products diffuse from the sediment down into the
basement where they are transported by the basement fluid and released to
the ocean. Here, we investigate the impact of this “second” route with
respect to transport, release and consumption of oxygen, nitrate, manganese,
nickel and cobalt on the basis of sediment cores retrieved from the Clarion
Clipperton Zone (CCZ) in the equatorial Pacific Ocean. We show that in this
abyssal ocean region characterised by low organic carbon burial and
sedimentation rates vast areas exist where the downward- and upward-directed
diffusive fluxes of oxygen meet so that the sediments are oxic throughout.
This is especially the case where sediments are thin or in the proximity of
faults. Oxygen diffusing upward from the basaltic crust into the sediment
contributes to the degradation of sedimentary organic matter. Where the
sediments are entirely oxic, nitrate produced in the upper sediment by
nitrification is lost both by upward diffusion into the bottom water and by
downward diffusion into the fluids circulating within the basement. Where
the oxygen profiles do not meet, they are separated by a suboxic sediment
interval characterised by Mn2+ in the porewater. Where porewater
Mn2+ in the suboxic zones remains low, nitrate consumption is low and
the sediment continues to deliver nitrate to the ocean bottom waters and
basement fluid. We observe that at elevated porewater manganese
concentrations, nitrate consumption exceeds production and nitrate diffuses
from the basement fluid into the sediment. Within the suboxic zone, not only
manganese but also cobalt and nickel are released into the porewater by
reduction of Mn oxides, diffusing towards the oxic–suboxic fronts above and
below where they precipitate, effectively removing these metals from the
suboxic zone and concentrating them at the two oxic–suboxic redox
boundaries. We show that not only do diffusive fluxes in the top part of
deep-sea sediments modify the geochemical composition over time but also
diffusive fluxes of dissolved constituents from the basement into the bottom
layers of the sediment. Hence, the palaeoceanographic interpretation of
sedimentary layers should carefully consider such deep secondary
modifications in order to prevent the misinterpretation of primary signatures.