Description: Empirical transfer functions are derived for predicting the total benthic nitrate loss(LNO3) and the net loss of dissolved inorganic nitrogen (LDIN) in marine sediments,equivalent to sedimentary denitrification. The functions are dynamic vertically integratedsediment models which require the rain rate of particulate organic carbon to the seafloor(RRPOC) and a proposed new variable(O2-NO3)bw (bottom water O2 concentration minus NO3-concentration) as the only input parameters. Applied globally to maps of RRPOC and(O2-NO3)bw on a 1° x 1° spatial resolution, the models predict a NO3- drawdown of 196 Tg yr-1 (LNO3)of which 153 – 155 Tg yr-1 is denitrified to N2 (LDIN). This is in good agreement with previous estimates using very different methods. Our approach implicitly accounts for fixed N loss via anammox, such that our findings do not support the idea that the relatively recent discovery of anammox in marine sediments might require current estimates of the global benthic marine N budget to be revised. The continental shelf (0 – 200 m) accounts for 〉50% of global LNO3 and LDIN, with slope (200 – 2000 m) and deep-sea (〉2000 m) sediments contributing ca. 30% and 20%, respectively. Denitrification in high-nitrate/low-oxygen regions such as oxygen minimum zones is significant (ca. 15 Tg N yr-1; 10% of global) despite covering only 1% of the seafloor. The data are used to estimate the net fluxes of nitrate (18 Tg N yr-1) and phosphate(27 Tg P yr-1) across the sediment-water interface. The benthic fluxes strongly deviate from Redfield composition, with globally averaged N:P, N:C and C:P values of 8.3, 0.067 and 122, respectively, indicating world-wide fixed N losses (by denitrification) relative to C and P. The transfer functions are designed to be coupled dynamically to general circulation models to better predict the feedback of sediments on pelagic nutrient cycling and dissolved O2 distributions.

Description: Geochemical data (CH4, SO42−, I−, Cl−, particulate organic carbon (POC), δ13C-CH4, and δ13C-CO2) are presented from the upper 30 m of marine sediment on a tectonic submarine accretionary wedge offshore southwest Taiwan. The sampling stations covered three ridges (Tai-Nan, Yung-An, and Good Weather), each characterized by bottom simulating reflectors, acoustic turbidity, and different types of faulting and anticlines. Sulfate and iodide concentrations varied little from seawater-like values in the upper 1–3 m of sediment at all stations; a feature that is consistent with irrigation of seawater by gas bubbles rising through the soft surface sediments. Below this depth, sulfate was rapidly consumed within 5–10 m by anaerobic oxidation of methane (AOM) at the sulfate-methane transition. Carbon isotopic data imply a mainly biogenic methane source. A numerical transport-reaction model was used to identify the supply pathways of methane and estimate depth-integrated turnover rates at the three ridges. Methane gas ascending from deep layers, facilitated by thrusts and faults, was by far the dominant term in the methane budget at all sites. Differences in the proximity of the sampling sites to the faults and anticlines mainly accounted for the variability in gas fluxes and depth-integrated AOM rates. By comparison, methane produced in situ by POC degradation within the modeled sediment column was unimportant. This study demonstrates that the geochemical trends in the continental margins offshore SW Taiwan are closely related to the different geological settings.

Description: Five sediment cores from cold seeps at the forearc off Costa Rica were used to explore the relationship between fluid advection, dissolved Ca concentrations in upward migrating fluids, and authigenic CaCO3 precipitation. A numerical transport-reaction model was used to determine rates of anaerobic oxidation of methane (AOM), CaCO3 precipitation, and benthic fluxes of solutes. Production of carbonate alkalinity and formation of authigenic carbonates is most intense at intermediate flow rates (3–40 cm a−1) and reduced under low and high flux conditions (0.1 and 200 cm a−1). Dissolved Ca concentrations observed in the vent fluids off Costa Rica cover a wide range between 4 and 31 mM, clearly exceeding seawater concentrations at two locations. Systematic model runs showed that high Ca concentrations in ascending fluids enhance the rate of authigenic carbonate production at moderate flow rates leading to an almost quantitative fixation of deeply derived Ca in authigenic carbonates. Hence, CaCO3 precipitation is not only controlled by Ca diffusing into the sediment from bottom water, but also by the Ca concentration in ascending fluids. Thus, Ca enriched fluids offer a reason for enhanced subsurface CaCO3 precipitation and the occurrence of carbonate caps on dewatering structures in the Central American fore-arc. Based on average precipitation rates deduced from the systematic model runs it is possible to give a rough estimate of the global Ca-fixation at cold seeps (∼2·1010 mol Ca a−1), which suggests that cold seeps are most likely not of key importance with respect to Ca cycling in the ocean.

Description: The phosphorus budget of the pre-human modern ocean is constrained applying the most recent estimates of the natural riverine, eolian, and ice-rafted input fluxes, the phosphorus burial in marine sediments, and the hydrothermal removal of dissolved phosphate from the deep ocean. This review of current flux estimates indicates that the phosphorus budget of the ocean is unbalanced since the accumulation of phosphorus in marine sediments and altered oceanic crust exceeds the continental input of particulate and dissolved phosphorus. The phosphorus mass balance is further tested considering the dissolved phosphate distribution in the deep water column, the marine export production of particulate organic matter, rain rates of phosphorus to the seafloor, benthic dissolved phosphate fluxes, and the organic carbon to phosphorus ratios in marine particles. These independent data confirm that the phosphate and phosphorus budgets were not at steadystate in the pre-human global ocean. The ocean is losing dissolved phosphate at a rate of ≥ 11.6 x 1010 mol yr-1 corresponding to a decline in the phosphate inventory of ≥ 4.5 % kyr-1. Benthic data show that phosphate is preferentially retained in pelagic deep-sea sediments where extended oxygen exposure times favor the degradation of particulate organic matter and the up-take of phosphate in manganese and iron oxides and hydroxides. Enhanced C : P regeneration ratios observed in the deep water column (〉400 m water depth) probably reflect the preferential burial of phosphorus in pelagic sediments. Excess phosphate is released from continental margin sediments deposited in low-oxygen environments. The dissolved oxygen threshold value for the enhanced release of dissolved phosphate is ~20 μM. Benthic phosphate fluxes increase drastically when oxygen concentrations fall below this value.

Description: Vast amounts of methane hydrates are potentially stored in sediments along the continental margins, owing their stability to low temperature – high pressure conditions. Global warming could destabilize these hydrates and cause a release of methane (CH 4) into the water column and possibly the atmosphere. Since the Arctic has and will be warmed considerably, Arctic bottom water temperatures and their future evolution projected by a climate model were analyzed. The resulting warming is spatially inhomogeneous, with the strongest impact on shallow regions affected by Atlantic inflow. Within the next 100 years, the warming affects 25% of shallow and mid-depth regions containing methane hydrates. Release of methane from melting hydrates in these areas could enhance ocean acidification and oxygen depletion in the water column. The impact of methane release on global warming, however, would not be significant within the considered time span.