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N2O production and consumption from stable isotopic and concentration data in the Peruvian coastal upwelling system

机译:N2O在秘鲁沿海上升系统中的稳定同位素和集中数据的生产和消费

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The ocean is an important source of nitrous oxide (N2O) to the atmosphere, yet the factors controlling N2O production and consumption in oceanic environments are still not understood nor constrained. We measured N2O 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 (similar to 5-16 degrees S, 75-81 degrees W) in December 2012 and January 2013. N2O concentrations varied from below equilibrium values in the oxygen deficient zone (ODZ) to up to 190 nmol L-1 in surface waters. We used a 3-D-reaction-advection-diffusion model to evaluate the rates and modes of N2O production in oxic waters and rates of N2O consumption versus production by denitrification in the ODZ. Intramolecular site preference in N2O isotopomer was relatively low in surface waters (generally -3 to 14 parts per thousand) 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(-1) off the Peru coast. Other evidence, e.g., the absence of a relationship between Delta N2O and apparent O-2 utilization and significant relationships between nitrate, a substrate during denitrification, and N2O isotopes, suggest that N2O production by incomplete denitrification or nitrifier-denitrification decoupled from aerobic organic matter remineralization are likely pathways for extreme N2O accumulation in newly upwelled surface waters. We observed imbalances between N2O production and consumption in the ODZ, with the modeled proportion of N2O consumption relative to production generally increasing with biogenic N-2. However, N2O production appeared to occur even where there was high N loss at the shallowest stations.
机译:海洋是氧化亚氮(N2O)的重要来源,但控制N2O生产和海洋环境消耗的因素仍未理解也不受到约束。我们测量了N 2 O浓度和同位素比率,以及O-2,营养和生物是N-2浓度,以及在秘鲁海岸的两次巡航期间在几个沿海站的硝酸盐和亚硝酸盐的同位素组成(类似于5-16℃ ,75-81摄氏度W)于2012年12月和2013年1月。N2O浓度从低于表面水中的氧缺陷区(ODZ)的平衡值低于高达190nmol L-1。我们使用了一个三维反作用 - 平流扩散模型来评估氧化物水中N2O产生的速率和模式,并通过奥兹中的反硝化对N2O消费的率。在N 2 O同位素中的分子内部位偏好在表面水中相对较低(通常为-3至14份/每千份),并与建模结果一起证实了硝化亚硝化或不完全的反硝化偶氮的优势,对应于高达0.6 Tg的流出n yr(-1)关闭秘鲁海岸。其他证据(例如,δN2O和明显O-2在硝酸的明显O-2使用和明显O-2利用率之间的关系和硝酸盐之间的显着关系)表明N2O通过不完全反硝化或硝化硝化物从有氧有机物分离的硝基脱氮结肠化可能是新升高的地表水中极端N2O积累的途径。我们观察到ODZ中N2O生产和消费之间的不平衡,相对于生产的N2O消耗的建模比例通常随生物元N-2的增加而增加。然而,即使在最浅的地方,也似乎发生了N2O产量。

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