The ocean is an important source of nitrous oxide (N 2 O) to the atmosphere, yet the factors controlling N 2 O production and consumption in oceanic environments are still not understood nor constrained. We measured N 2 O concentrations and isotopomer ratios, as well as O 2 , nutrient and biogenic N 2 concentrations, and the isotopic compositions of nitrate and nitrite at several coastal stations during two cruises off the Peru coast (~5-16°S, 75-81°W) in December 2012 and January 2013. N 2 O concentrations varied from below equilibrium values in the oxygen deficient zone (ODZ) to up to 190 nmol L À1 in surface waters. We used a 3-D-reaction-advection-diffusion model to evaluate the rates and modes of N 2 O production in oxic waters and rates of N 2 O consumption versus production by denitrification in the ODZ. Intramolecular site preference in N 2 O isotopomer was relatively low in surface waters (generally À3 to 14‰) and together with modeling results, confirmed the dominance of nitrifier-denitrification or incomplete denitrifier-denitrification, corresponding to an efflux of up to 0.6 Tg N yr À1 off the Peru coast. Other evidence, e.g., the absence of a relationship between ΔN 2 O and apparent O 2 utilization and significant relationships between nitrate, a substrate during denitrification, and N 2 O isotopes, suggest that N 2 O production by incomplete denitrification or nitrifier-denitrification decoupled from aerobic organic matter remineralization are likely pathways for extreme N 2 O accumulation in newly upwelled surface waters. We observed imbalances between N 2 O production and consumption in the ODZ, with the modeled proportion of N 2 O consumption relative to production generally increasing with biogenic N 2 . However, N 2 O production appeared to occur even where there was high N loss at the shallowest stations.
Selective removal of nitrogen (N) and phosphorus (P) from the marine dissolved organic matter (DOM) pool has been reported in several regional studies. Because DOM is an important advective/mixing pathway of carbon (C) export from the ocean surface layer and its non-Redfieldian stoichiometry would affect estimates of marine export production per unit N and P, we investigated the stoichiometry of marine DOM and its remineralization globally using a compiled DOM data set. Marine DOM is enriched in C and N compared to Redfield stoichiometry, averaging 317:39:1 and 810:48:1 for C:N:P within the degradable and total bulk pools, respectively. Dissolved organic phosphorus (DOP) is found to be preferentially remineralized about twice as rapidly with respect to the enriched C:N stoichiometry of marine DOM. Biogeochemical simulations with the Biogeochemical Elemental Cycling model using Redfield and variable DOM stoichiometry corroborate the need for non-Redfield dynamics to match the observed DOM stoichiometry. From our model simulations, preferential DOP remineralization is found to increase the strength of the biological pump by~9% versus the case of Redfield DOM cycling. Global net primary productivity increases~10% including an increase in marine nitrogen fixation of~26% when preferential DOP remineralization and direct utilization of DOP by phytoplankton are included. The largest increases in marine nitrogen fixation, net primary productivity, and carbon export are observed within the western subtropical gyres, suggesting the lateral transfer of P in the form of DOP from the productive eastern and poleward gyre margins may be important for sustaining these processes downstream in the subtropical gyres.
The allochthonous supply of dissolved organic nitrogen (DON) from gyre margins into the interior of the ocean's oligotrophic subtropical gyres potentially provides an important source of new N to gyre surface waters, thus sustaining export production. This process requires that a fraction of the transported DON be available to euphotic zone photoautotroph communities via mineralization. In this study, we investigated the biological and physical controls on the distribution and fate of DON within global ocean surface waters. Inputs of nitrate to the euphotic zone at upwelling zones fuel net accumulation of a DON pool that appears to resist rapid microbial remineralization, allowing subsequent advective transport into the subtropical gyres. Zonal gradients in DON concentrations across these gyres imply a DON sink in the surface layer. Assessment of the physical dynamics of gyre circulation and winter mixing revealed a pathway for DON removal from the mixed layer via vertical transport to the deep euphotic zone, which establishes the observed zonal gradients. Incubation experiments from the Florida Straits indicated surface‐accumulated DON was largely resistant (over a few months) to utilization by the extant surface bacterioplankton community. In contrast, this same material was remineralized three times more rapidly when exposed to upper mesopelagic bacterioplankton. These results suggest the primary fate of surface DON to be removal via vertical mixing and subsequent mineralization below the mixed layer, implying a limited role for direct DON support of gyre export production from the surface layer. DON may contribute to export production at the eastern edges of the subtropical gyres, but only after its mineralization within the deep euphotic zone.
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