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Using ship-borne observations of methane isotopic ratio in the Arctic Ocean to understand methane sources in the Arctic

机译:在北冰洋中使用甲烷同位素比例的甲烷同位素比例来了解北极的甲烷来源

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摘要

Characterizing methane sources in the Arctic remains challenging due to the remoteness, heterogeneity and variety of such emissions. In situ campaigns provide valuable datasets to reduce these uncertainties. Here we analyse data from the summer 2014 SWERUS-C3 campaign in the eastern Arctic Ocean, off the shore of Siberia and Alaska. Total concentrations of methane, as well as relative concentrations of 12CH4 and 13CH4, were measured continuously during this campaign for 35 d in July and August. Using a?chemistry-transport model, we link observed concentrations and isotopic ratios to regional emissions and hemispheric transport structures. A?simple inversion system helped constrain source signatures from wetlands in Siberia and Alaska, and oceanic sources, as well as the isotopic composition of lower-stratosphere air masses. The variation in the signature of lower-stratosphere air masses, due to strongly fractionating chemical reactions in the stratosphere, was suggested to explain a?large share of the observed variability in isotopic ratios. These results point towards necessary efforts to better simulate large-scale transport and chemistry patterns to make relevant use of isotopic data in remote areas. It is also found that constant and homogeneous source signatures for each type of emission in a?given region (mostly wetlands and oil and gas industry in our case at high latitudes) are not compatible with the strong synoptic isotopic signal observed in the Arctic. A?regional gradient in source signatures is highlighted between Siberian and Alaskan wetlands, the latter having lighter signatures (more depleted in 13C). Finally, our results suggest that marine emissions of methane from Arctic continental-shelf sources are dominated by thermogenic-origin methane, with a?secondary biogenic source as well.
机译:由于偏差,异质性和各种各种排放,北极地区的甲烷来源仍然挑战。原位活动提供有价值的数据集,以减少这些不确定性。在这里,我们分析了2014年夏季的夏季C3在东北角海洋,偏离西伯利亚和阿拉斯加州的数据。在7月和8月在此次活动期间,在这项运动期间连续测量甲烷的总浓度,以及12CH4和13CH4的相对浓度。使用a?化学传输模型,我们将观察到的浓度和同位素比率与区域排放和半球运输结构联系起来。 a?简单的反演系统有助于约束西伯利亚和阿拉斯加和阿拉斯加和海洋来源的湿地的源签名,以及低层间空气群众的同位素组成。由于平流层中强烈分馏的化学反应,较低平流层空气群众签名的变化被提出了解释了同位素比例的观察到变异性的大量。这些结果指出了更好地模拟大规模运输和化学模式的必要努力,以便在偏远地区进行同位素数据的相关使用。还发现,对于每种类型的排放中的恒定和均匀的源签名在1个给定的区域(大多数湿地和石油和天然气行业,在高纬度地区)与在北极中观察到的强偶发性同位素信号不相容。 a?在西伯利亚和阿拉斯加湿地之间突出了源签名中的区域梯度,后者具有更轻的签名(在13c中更耗尽)。最后,我们的结果表明,北极大陆架子源的甲烷海洋排放由热原甲烷主导,其中α二次生物源。

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