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Biogeochemical context impacts seawater pH changes resulting from atmospheric sulfur and nitrogen deposition

机译:生物地球化学背景影响由大气硫和氮沉积引起的海水pH变化

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摘要

Seawater acidification can be induced both by absorption of atmospheric carbon dioxide (CO2) and by atmospheric deposition of sulfur and nitrogen oxides and ammonia. Their relative significance, interplay, and dependency on water column biogeochemistry are not well understood. Using a simple biogeochemical model we show that the initial conditions of coastal systems are not only relevant for CO2-induced acidification but also for additional acidification due to atmospheric acid deposition. Coastal areas undersaturated with respect to CO2 are most vulnerable to CO2-induced acidification but are relatively least affected by additional atmospheric deposition-induced acidification. In contrast, the pH of CO2-supersaturated systems is most sensitive to atmospheric deposition. The projected increment in atmospheric CO2 by 2100 will increase the sensitivity of coastal systems to atmospheric deposition-induced acidification by up to a factor 4, but the additional annual change in proton concentration is at most 28%.
机译:海水的酸化既可以通过吸收大气中的二氧化碳(CO2),也可以通过大气中硫,氮氧化物和氨的沉积来诱导。它们的相对重要性,相互作用和对水柱生物地球化学的依赖性尚不十分清楚。使用简单的生物地球化学模型,我们显示了沿海系统的初始条件不仅与二氧化碳诱导的酸化有关,而且与大气酸沉积引起的其他酸化有关。相对于CO2饱和度不足的沿海地区最容易受到CO2诱导的酸化的影响,但受其他大气沉积物诱导的酸化的影响相对最小。相反,CO2过饱和系统的pH对大气沉积最敏感。预计到2100年大气CO2的增加将使沿海系统对大气沉积诱导的酸化的敏感性增加多达4倍,但是质子浓度的额外年度变化最多为28%。

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