加勒比海卡里亚科海沟和挪威德拉姆斯峡湾两个厌氧环境中的氮/氩和氮同位素比率

Francis A. Richards , Bruce B. Benson
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引用次数: 69

摘要

利用质谱法测量氮/氩和氮同位素比率,研究了两个厌氧海洋环境(加勒比海的卡里亚科海沟和挪威的德拉姆斯峡湾)中有机物分解产生的氮的去向。这些水中的N2/A值比大气中溶解气体的预期值要大。通过假设A浓度在生物学上不受影响,可以计算出N2的过量量。这与有机物分解所产生的氮的含量是一致的。后者的值是根据观察到的氮化合物浓度和观察到的无机磷酸盐浓度或从水中消耗的氧(游离或结合在硫酸盐离子中的)的量计算出来的。结果表明,生物源氮与大气溶解氮的氮同位素比值存在显著差异。结果表明,游离氮很可能只能通过作为中间体形成的硝酸盐的反硝化作用从有机物中生成。
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Nitrogen/argon and nitrogen isotope ratios in two anaerobic environments, the Cariaco Trench in the Caribbean Sea and Dramsfjord, Norway

Mass spectrometric measurements of nitrogen/argon and nitrogen isotope ratios have been used to examine the fate of nitrogen arising from the decomposition of organic matter in two anaerobic marine environments, the Cariaco Trench in the Caribbean Sea and the Dramsfjord in Norway.

Values of N2/A in these waters are larger than would be expected from dissolved atmospheric gases. By assumingthat the A concentration is biologically unaffected, the excess quantities of N2 can be calculated. These are in good agreement with the amounts of nitrogen which would be expected to arise from the decomposition of organic matter. The latter values are computed from the observed concentrations of nitrogen compounds and either the observed concentrations of inorganic phosphate or the amounts of oxygen (either free or bound in the sulphate ion) consumed from the water.

It is shown that nitrogen isotope ratios are markedly different in the nitrogen of biogenic origin from those in nitrogen dissolved from the atmosphere.

It is shown that it is probable that free nitrogen can be formed from organic matter only through the denitrification of nitrate, formed as an intermediate.

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