Description: Highlights • Very high rates of dissimilatory nitrate reduction to ammonium by Thioploca. • Non-steady state model predicts Thioploca survival on intracellular nitrate reservoir. • Ammonium release by Thioploca may be coupled to pelagic N loss by anammox. • Thioploca may contribute to anammox long after bottom water nitrate disappearance. • Model indicates that benthic foraminifera account for 90% of benthic N2 production. Abstract Benthic N cycling in the Peruvian oxygen minimum zone (OMZ) was investigated at ten stations along 12oS from the middle shelf (74 m) to the upper slope (1024 m) using in situ flux measurements, sediment biogeochemistry and modelling. Middle shelf sediments were covered by mats of the filamentous bacteria Thioploca spp. and contained a large ‘hidden’ pool of nitrate that was not detectable in the porewater. This was attributed to a biological nitrate reservoir stored within the bacteria to oxidize sulfide to sulfate during ‘dissimilatory nitrate reduction to ammonium’ (DNRA). The extremely high rates of DNRA on the shelf (15.6 mmol m-2 d-1 of N), determined using an empirical steady-state model, could easily supply all the ammonium requirements for anammox in the water column. The model further showed that denitrification by foraminifera may account for 90% of N2 production at the lower edge of the OMZ. At the time of sampling, dissolved oxygen was below detection limit down to 400 m and the water body overlying the shelf had stagnated, resulting in complete depletion of nitrate and nitrite. A decrease in the biological nitrate pool was observed on the shelf during fieldwork concomitant with a rise in porewater sulfide levels in surface sediments to 2 mM. Using a non-steady state model to simulate this natural anoxia experiment, these observations were shown to be consistent with Thioploca surviving on a dwindling intracellular nitrate reservoir to survive the stagnation period. The model shows that sediments hosting Thioploca are able to maintain high ammonium fluxes for many weeks following stagnation, potentially sustaining pelagic N loss by anammox. In contrast, sulfide emissions remain low, reducing the economic risk to the Peruvian fishery by toxic sulfide plume development.

Description: The upwelling area off North-West Africa is characterized by high export production, high nitrate and low oxygen concentration in bottom waters. The underlying sediment consists of sands that cover most of the continental shelf. Due to their permeability sands allow for fast advective pore water transport and can exhibit high rates of nitrogen (N) loss via denitrification as reported for anthropogenically eutrophied regions. However, N loss from sands underlying naturally eutrophied waters is not well studied, and in particular, N loss from the North-West African shelf is poorly constrained. During two research cruises in April/May 2010/2011, sediment was sampled along the North-West African shelf and volumetric denitrification rates were measured in sediment layers down to 8 cm depth using slurry incubations with 15N-labeled nitrate. Areal N loss was calculated by integrating volumetric rates down to the nitrate penetration depth derived from pore water profiles. Areal N loss was neither correlated with water depth nor with bottom water concentrations of nitrate and oxygen but was strongly dependent on sediment grain size and permeability. The derived empirical relation between benthic N loss and grains size suggests that pore water advection is an important regulating parameter for benthic denitrification in sands and further allowed extrapolating rates to an area of 53,000 km2 using detailed sediment maps. Denitrification from this region amounts to 995 kt yr-1 (average 3.6 mmol m-2 d-1) which is 4 times higher than previous estimates based on diffusive pore water transport. Sandy sediments cover 50-60% of the continental shelf and thus may contribute significantly to the global benthic N loss.

Description: Highlights • Sulphidic event on the shelf resulted in a temporal imbalance of the benthic N cycle. • Bacterial NOx storage is a major source of oxidative power during euxinia. • Peruvian shelf and upper slope sediments are strong recycling sites of fixed N. Abstract Oxygen minimum zones (OMZ) are key regions for fixed nitrogen loss in both the sediments and the water column. During this study, the benthic contribution to N cycling was investigated at ten sites along a depth transect (74–989 m) across the Peruvian OMZ at 12 °S. O2 levels were below detection limit down to ~ 500 m. Benthic fluxes of N2, NO3–, NO2–, NH4+, H2S and O2 were measured using benthic landers. Flux measurements on the shelf were made under extreme geochemical conditions consisting of a lack of O2, NO3– and NO2– in the bottom water and elevated seafloor sulphide release. These particular conditions were associated with a large imbalance in the benthic nitrogen cycle. The sediments on the shelf were densely covered by filamentous sulphur bacteria Thioploca, and were identified as major recycling sites for DIN releasing high amounts of NH4+up to 21.2 mmol m−2 d−1 that were far in excess of NH4+release by ammonification. This difference was attributed to dissimilatory nitrate (or nitrite) reduction to ammonium (DNRA) that was partly being sustained by NO3– stored within the sulphur oxidizing bacteria. Sediments within the core of the OMZ (ca. 200 to 400 m) also displayed an excess flux of N of 3.5 mmol m−2 d−1 mainly as N2. Benthic nitrogen and sulphur cycling in the Peruvian OMZ appears to be particularly susceptible to bottom water fluctuations in O2, NO3−and NO2−, and may accelerate the onset of pelagic euxinia when NO3−and NO2−become depleted.

Description: The squat lobster Pleuroncodes monodon is a key species of the highly productive, but oxygen-poor upwelling system of the Eastern Tropical South Pacific. Observations of P. monodon in the water column off Peru have led to the hypothesis that anoxic conditions force this otherwise primarily benthic species to adopt a pelagic lifestyle. Here we show that off Peru, P. monodon can be found in the oxygenated surface water, but also on the anoxic seafloor. Our physiological experiments demonstrate that juvenile and adult specimens have a very low critical respiratory pO2 of 0.5 kPa and that adults survive anoxia for 30.5–70.5 h. Anoxic conditions at the seafloor should therefore force P. monodon to regularly migrate to the oxic surface layer in order to restore energy reserves and recycle metabolic end products of anaerobic metabolism. It was recently estimated that the ammonium supply mediated by diel vertical migrations (DVMs) of zooplankton and nekton considerably fuels bacterial anaerobic ammonium oxidation—a major loss process for fixed nitrogen in the ocean. These estimates were based on the implicit assumption that anoxia does not result in a down-regulation of ammonium excretion. We here show that exposure to anoxia elicits a fourfold reduction in ammonium excretion from 2.1 ± 0.6 µmol h−1 g dry weight−1 under normoxic to 0.5 ± 0.6 µmol h−1 g DW−1 under anoxic conditions in P. monodon. Estimates of ammonium supply to the anoxic core of oxygen minimum zones via DVM therefore are likely too high.

Description: This study investigates the biogeochemical processes that control the benthic fluxes of dissolved nitrogen (N) species in Boknis Eck - a 28 m deep site in the Eckernförde Bay (southwestern Baltic Sea). Bottom water oxygen concentrations (O2-BW) fluctuate greatly over the year at Boknis Eck, being well-oxygenated in winter and experiencing severe bottom water hypoxia and even anoxia in late summer. The present communication addresses the winter situation (February 2010). Fluxes of ammonium (NH4+), nitrate (NO3-) and nitrite (NO2-) were simulated using a benthic model that accounted for transport andbiogeochemical reactions and constrained with ex situ flux measurements and sediment geochemical analysis. The sediments were a net sink for NO3- (-0.35 mmol m-2 d-1 of NO3-), of which 75% was ascribed to dissimilatory reduction of nitrate to ammonium (DNRA) by sulfide oxidizing bacteria, and 25% to NO3- reduction to NO2- by denitrifying microorganisms. NH4+ fluxes were high (1.74 mmol m-2d-1 of NH4+), mainly due to the degradation of organic nitrogen, and directed out of the sediment. NO2-fluxes were negligible. The sediments in Boknis Eck are, therefore, a net source of dissolved inorganic nitrogen(DIN = NO3- + NO2- + NH4+) during winter. This is in large part due to bioirrigation, which accounts for 76% of the benthic efflux of NH4+, thus reducing the capacity for nitrification of NH4+. The combined rate of fixed N loss by denitrification and anammox was estimated at 0.08 mmol m-2 d-1 of N2, which is at the lower end of previously reported values. A systematic sensitivity analysis revealed that denitrification and anammox respond strongly and positively to the concentration of NO3- in the bottomwater (NO3-BW).Higher O2-BW decreases DNRA and denitrification but stimulates both anammox and the contribution ofanammox to total N2 production (%Ramx). A complete mechanistic explanation of these findings is provided. Our analysis indicates that nitrification is the geochemical driving force behind the observed correlation between %Ramx and water depth in the seminal study of Dalsgaard et al. (2005). Despite remaining uncertainties, the results provide a general mechanistic framework for interpreting the existing knowledge of N-turnover processes and fluxes in continental margin sediments, as well as predicting the types of environment where these reactions are expected to occur prominently.

Description: Benthic nitrogen (N) cycling was investigated at six stations along a transect traversing the Peruvian oxygen minimum zone (OMZ) at 11 °S. An extensive dataset including porewater concentration profiles and in situ benthic fluxes of nitrate (NO3–), nitrite (NO2–) and ammonium (NH4+) was used to constrain a 1–D reaction–transport model designed to simulate and interpret the measured data at each station. Simulated rates of nitrification, denitrification, anammox and dissimilatory nitrate reduction to ammonium (DNRA) by filamentous large sulfur bacteria (e.g. Beggiatoa and Thioploca) were highly variable throughout the OMZ yet clear trends were discernible. On the shelf and upper slope (80 – 260 m water depth) where extensive areas of bacterial mats were present, DNRA dominated total N turnover (less-than-or-equals, slant 2.9 mmol N m–2 d–1) and accounted for greater-or-equal, slanted 65 % of NO3– + NO2– uptake by the sediments from the bottom water. Nonetheless, these sediments did not represent a major sink for dissolved inorganic nitrogen (DIN = NO3– + NO2– + NH4+) since DNRA reduces NO3– and, potentially NO2–, to NH4+. Consequently, the shelf and upper slope sediments were recycling sites for DIN due to relatively low rates of denitrification and high rates of ammonium release from DNRA and ammonification of organic matter. This finding contrasts with the current opinion that sediments underlying OMZs are a strong sink for DIN. Only at greater water depths (300 – 1000 m) did the sediments become a net sink for DIN. Here, denitrification was the major process (less-than-or-equals, slant 2 mmol N m–2 d–1) and removed 55 – 73 % of NO3– and NO2– taken up by the sediments, with DNRA and anammox accounting for the remaining fraction. Anammox was of minor importance on the shelf and upper slope yet contributed up to 62 % to total N2 production at the 1000 m station. The results indicate that the partitioning of oxidized N (NO3–, NO2–) into DNRA or denitrification is a key factor determining the role of marine sediments as DIN sinks or recycling sites. Consequently, high measured benthic uptake rates of oxidized N within OMZs do not necessarily indicate a loss of fixed N from the marine environment.

Description: In situ methane emission measurements from sediments are combined with water column backscatter anomalies recorded with an Acoustic Doppler Current Profiler (ADCP) integrated on a benthic observatory. During cruise SO191 to the Hikurangi Margin (New Zealand), the Fluid Flux Observatory (FLUFO) was deployed at a cold seep site at Omakere Ridge. The sediments incubated in the two benthic chambers of FLUFO contained seep-associated fauna, including small and larger tubeworms, juvenile bivalves of the genus Acharax and some juvenile clams. The first 26 h of in situ incubation revealed low to moderate methane fluxes of 0.01 to 0.4 mmol m− 2 d− 1 into the overlying water of the backup and flux chamber, respectively. In the following sampling sequence, however, the methane concentration in the flux chamber reached 3-fold higher concentrations whereas the methane concentration in the backup chamber remained low and unchanged. Simultaneous to the sudden methane increase, a significant backscatter anomaly was recorded and persisted for 30 min and covered the entire depth range (100 m) of the upward looking ADCP. Data analyses revealed that a single-phase plume (no bubbles) outburst likely occurred during this time. While bubbles appeared to be present during some periods, plume simulations revealed that the volume of gas required (rate of 8 ton/day) does not support a bubble plume. A second data set was obtained during lander deployments at Rock Garden where visual observations by ROV confirmed the transient pattern of free gas injection into the water column. Acoustic flares and methane concentration increase in the bottom water hint towards a pressure (tidal) induced discharge mechanism. The presented data demonstrate the temporal and spatial variability of seabed methane emission, and very short methane signal lifetime in the water column (hours to a few days) due to turbulent diffusion. Both have to be considered when methane budgets are extrapolated from single methane emission rates.

Description: This study combines sediment geochemical analysis, in situ benthic lander deployments and numerical modeling to quantify the biogeochemical cycles of carbon and sulfur and the associated rates of Gibbs energy production at a novel methane seep. The benthic ecosystem is dominated by a dense population of tube-building ampharetid polychaetes and conspicuous microbial mats were unusually absent. A 1D numerical reaction-transport model, which allows for the explicit growth of sulfide and methane oxidizing microorganisms, was tuned to the geochemical data using a fluid advection velocity of 14 cm yr−1. The fluids provide a deep source of dissolved hydrogen sulfide and methane to the sediment with fluxes equal to 4.1 and 18.2 mmol m−2 d−1, respectively. Chemosynthetic biomass production in the subsurface sediment is estimated to be 2.8 mmol m−2 d−1 of C biomass. However, carbon and oxygen budgets indicate that chemosynthetic organisms living directly above or on the surface sediment have the potential to produce 12.3 mmol m−2 d−1 of C biomass. This autochthonous carbon source meets the ampharetid respiratory carbon demand of 23.2 mmol m−2 d−1 to within a factor of 2. By contrast, the contribution of photosynthetically-fixed carbon sources to ampharetid nutrition is minor (3.3 mmol m−2 d−1 of C). The data strongly suggest that mixing of labile autochthonous microbial detritus below the oxic layer sustains high measured rates of sulfate reduction in the uppermost 2 cm of the sulfidic sediment (100–200 nmol cm−3 d−1). Similar rates have been reported in the literature for other seeps, from which we conclude that autochthonous organic matter is an important substrate for sulfate reducing bacteria in these sediment layers. A system-scale energy budget based on the chemosynthetic reaction pathways reveals that up to 8.3 kJ m−2 d−1 or 96 mW m−2 of catabolic (Gibbs) energy is dissipated at the seep through oxidation reactions. The microorganisms mediating sulfide oxidation and anaerobic oxidation of methane (AOM) produce 95% and 2% of this energy flux, respectively. The low power output by AOM is due to strong bioenergetic constraints imposed on the reaction rate by the composition of the chemical environment. These constraints provide a high potential for dissolved methane efflux from the sediment (12.0 mmol m−2 d−1) and indicates a much lower efficiency of (dissolved) methane sequestration by AOM at seeps than considered previously. Nonetheless, AOM is able to consume a third of the ascending methane flux (5.9 mmol m−2 d−1 of CH4) with a high efficiency of energy expenditure (35 mmol CH4 kJ−1). It is further proposed that bioenergetic limitation of AOM provides an explanation for the non-zero sulfate concentrations below the AOM zone observed here and in other active and passive margin sediments.

Description: Current de-oxygenation of the oceans is associated with severe habitat loss and distinct changes in the species composition of bentho-pelagic communities. We investigated the distributions of epibenthic megafauna across the Peruvian OMZ (11°S) at water depths ranging from ∼80 to 1000 m water depth using sea floor images. Likely controls of distributions were adressed by combining the abundances of major groups with geochemical parameters and sea-floor topography. In addition to bottom-water oxygen levels and organic-carbon availability, particular emphasis is laid on the effects of local hydrodynamics. Beside the occurrence of microbial mats at the shelf and upper slope, distinct zones of highly abundant megafauna, dominated by gastropods (900 ind. m−2), ophiuroids (140 ind. m−2), and pennatulaceans (20 ind. m−2), were observed at the lower boundary of the OMZ. Their distribution extended from 460 m water depth (O2 levels 〈 2 μM), where gastropods were abundant, to 680 m (O2 ∼6 μM) where epifaunal abundances declined sharply. Bottom water O2 represents a major factor that limits the ability of metazoans to invade deeply into the OMZ where they could have access to labile organic carbon. However, depending on their feeding mode, the distribution of organisms appeared to be related to local hydrodynamics caused by the energy dissipation of incipient internal M2 tides affecting the suspension, transport and deposition of food particles. This was particularly evident in certain sections of the investigated transect. At these potentially critical sites, energy dissipation of internal tides is associated with high bottom shear stress and high turbulences and coincides with elevated turbidity levels in the benthic boundary layer, increased Zr/Al-ratios, low sedimentation rates as well as a shift in the grain size towards coarser particles. In or near such areas, abundant suspension-feeding organisms, such as ophiuroids, pennatulaceans, and tunicates were present, whereas deposit-feeding gastropods were absent. The influence of local hydrodynamic conditions on the distribution of epibenthic organisms has been neglected in OMZ studies, although it has been considered in other settings.