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Minimal geological methane emissions during the Younger Dryas-Preboreal abrupt warming event

机译:年轻的德里亚斯河-前波雷阿尔的突然变暖事件中的地质甲烷排放量最小

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摘要

Methane (CH4) is a powerful greenhouse gas and plays a key part in global atmospheric chemistry. Natural geological emissions (fossil methane vented naturally from marine and terrestrial seeps and mud volcanoes) are thought to contribute around 52 teragrams of methane per year to the global methane source, about 10 per cent of the total, but both bottom-up methods (measuring emissions)(1) and top-down approaches (measuring atmospheric mole fractions and isotopes)(2) for constraining these geological emissions have been associated with large uncertainties. Here we use ice core measurements to quantify the absolute amount of radiocarbon-containing methane ((CH4)-C-14) in the past atmosphere and show that geological methane emissions were no higher than 15.4 teragrams per year (95 per cent confidence), averaged over the abrupt warming event that occurred between the Younger Dryas and Preboreal intervals, approximately 11,600 years ago. Assuming that past geological methane emissions were no lower than today(3,4), our results indicate that current estimates of today's natural geological methane emissions (about 52 teragrams per year)(1,2) are too high and, by extension, that current estimates of anthropogenic fossil methane emissions(2) are too low. Our results also improve on and confirm earlier findings(5-7) that the rapid increase of about 50 per cent in mole fraction of atmospheric methane at the Younger Dryas-Preboreal event was driven by contemporaneous methane from sources such as wetlands; our findings constrain the contribution from old carbon reservoirs (marine methane hydrates(8), permafrost(9) and methane trapped under ice(10)) to 19 per cent or less (95 per cent confidence). To the extent that the characteristics of the most recent deglaciation and the Younger Dryas-Preboreal warming are comparable to those of the current anthropogenic warming, our measurements suggest that large future atmospheric releases of methane from old carbon sources are unlikely to occur.
机译:甲烷(CH4)是一种强大的温室气体,在全球大气化学中起着关键作用。自然地质排放(从海洋和陆地渗出物以及火山泥中自然排放的化石甲烷)被认为每年为全球甲烷源贡献了约52太克甲烷,约占总量的10%,但两种方法都是自下而上的(测量排放(1)和自上而下的方法(测量大气中的摩尔分数和同位素)(2),以限制这些地质排放,这具有很大的不确定性。在这里,我们使用冰芯测量来量化过去大气中的绝对含量的含放射性碳的甲烷((CH4)-C-14),并显示地质甲烷的排放量每年不高于15.4兆克(置信度为95%),大约在11600年前,在Younger Dryas和Preboreal间隔之间发生的突然变暖事件中得到平均。假设过去的地质甲烷排放量不低于今天(3,4),我们的结果表明,当前对当今自然地质甲烷排放量的估算(每年约52兆克)(1,2)太高了,因此,目前对人为化石甲烷排放量的估算(2)太低。我们的结果也改进并证实了较早的发现(5-7),在年轻的得里亚斯-普雷沃里尔事件中,大气甲烷的摩尔分数迅速增加约50%,是由湿地等来源的同期甲烷推动的;我们的发现将旧碳库(海洋甲烷水合物(8),多年冻土(9)和被冰夹住的甲烷(10))的贡献限制在19%或更少(95%置信度)。在一定程度上,最近一次冰消和新德里斯-德莱亚斯-前原冰的变暖的特征可与当前的人为变暖的特征相提并论,我们的测量结果表明,未来不太可能从旧碳源向大气中释放大量甲烷。

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  • 来源
    《Nature》 |2017年第7668期|443-446|共4页
  • 作者单位

    Univ Rochester, Dept Earth & Environm Sci, 601 Elmwood Ave, Rochester, NY 14627 USA;

    ANSTO, Locked Bag 2001, Kirrawee Dc, NSW 2232, Australia;

    Natl Inst Water & Atmospher Res NIWA, POB 14901,301 Evans Bay Parade, Wellington, New Zealand;

    Natl Inst Water & Atmospher Res NIWA, POB 14901,301 Evans Bay Parade, Wellington, New Zealand;

    Oregon State Univ, Coll Earth Ocean & Atmospher Sci, Corvallis, OR 97331 USA;

    Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA|Univ Bern, Inst Phys, CH-3012 Bern, Switzerland;

    Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA;

    ANSTO, Locked Bag 2001, Kirrawee Dc, NSW 2232, Australia;

    Oregon State Univ, Coll Earth Ocean & Atmospher Sci, Corvallis, OR 97331 USA;

    Oregon State Univ, Coll Earth Ocean & Atmospher Sci, Corvallis, OR 97331 USA;

    Univ Grenoble Alpes, CNRS, LGGE, UMR 5183, F-38041 Grenoble, France;

    Oregon State Univ, Coll Earth Ocean & Atmospher Sci, Corvallis, OR 97331 USA|Univ Utah, Dept Atmospher Sci, Salt Lake City, UT 84112 USA;

    Oregon State Univ, Coll Earth Ocean & Atmospher Sci, Corvallis, OR 97331 USA|Univ Cambridge, Dept Earth Sci, Cambridge CB2 3EQ, England;

    Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA|Univ Paris Saclay, Lab Sci Climat & Environm, LSCE IPSL, CEA CNRS UVSQ, F-91198 Gif Sur Yvette, France;

    Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA;

    Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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