[1] Nitrogen isotopes are an important tool for evaluating past biogeochemical cycling from the paleoceanographic record. However, bulk sedimentary nitrogen isotope ratios, which can be determined routinely and at minimal cost, may be altered during burial and early sedimentary diagenesis, particularly outside of continental margin settings. The causes and detailed mechanisms of isotopic alteration are still under investigation. Case studies of the Mediterranean and South China Seas underscore the complexities of investigating isotopic alteration. In an effort to evaluate the evidence for alteration of the sedimentary N isotopic signal and try to quantify the net effect, we have compiled and compared data demonstrating alteration from the published literature. A >100 point comparison of sediment trap and surface sedimentary nitrogen isotope values demonstrates that, at sites located off of the continental margins, an increase in sediment 15 N/ 14 N occurs during early burial, likely at the seafloor. The extent of isotopic alteration appears to be a function of water depth. Depth-related differences in oxygen exposure time at the seafloor are likely the dominant control on the extent of N isotopic alteration. Moreover, the compiled data suggest that the degree of alteration is likely to be uniform through time at most sites so that bulk sedimentary isotope records likely provide a good means for evaluating relative changes in the global N cycle.Citation: Robinson, R. S., et al. (2012), A review of nitrogen isotopic alteration in marine sediments, Paleoceanography, 27, PA4203,

Global warming is expected to decrease ocean oxygen concentrations by less solubility of surface ocean and change in ocean circulation. The associated expansion of the oxygen minimum zone would have adverse impacts on marine organisms and ocean biogeochemical cycles. Oxygen reduction is expected to persist for a thousand years or more, even after atmospheric carbon dioxide stops rising. However, long-term changes in ocean oxygen and circulation are still unclear. Here we simulate multimillennium changes in ocean circulation and oxygen under doubling and quadrupling of atmospheric carbon dioxide, using a fully coupled atmosphere-ocean general circulation model and an offline biogeochemical model. In the first 500 years, global oxygen concentration decreases, consistent with previous studies. Thereafter, however, the oxygen concentration in the deep ocean globally recovers and overshoots at the end of the simulations, despite surface oxygen decrease and weaker Atlantic meridional overturning circulation. This is because, after the initial cessation, the recovery and overshooting of deep ocean convection in the Weddell Sea enhance ventilation and supply oxygen-rich surface waters to deep ocean. Another contributor to deep ocean oxygenation is seawater warming, which reduces the export production and shifts the organic matter remineralization to the upper water column. Our results indicate that the change in ocean circulation in the Southern Ocean potentially drives millennial-scale oxygenation in deep ocean, which is opposite to the centennial-scale global oxygen reduction and general expectation.

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[1] To investigate the iron cycle at Station A4 in the Oyashio region of the western subarctic Pacific, we developed a 1-D ecosystem model consisting of 14 components including the iron cycle. The parameters associated with the iron cycle were optimized by assimilating monthly averaged data from time series observations for depth-integrated net primary production, nitrate, silicate, dissolved and particulate iron within the surface mixed layer (ML) and at two depths (200 and 300 m depth). The model successfully reproduced the observations and demonstrated that (1) on an annual basis, winter mixing of subsurface water supplies more dissolved iron (Fe d ) to the ML than does dust dissolution, (2) Fe d concentration in the ML rapidly declines to near-depletion during the peak period of the diatom bloom in spring, which results in an increasing consumption ratio of silicate to nitrogenous nutrients by diatoms as they become more iron-limited, causing a more rapid decrease of silicate compared to that of nitrogenous nutrients in the ML, followed by the silicate limitation of diatoms, and (3)