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An updated anthropogenic CO2 inventory in the Atlantic Ocean

机译:大西洋的最新人为二氧化碳清单

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摘要

[1] This paper presents a comprehensive analysis of the basin-wide inventory of anthropogenic CO_2 in the Atlantic Ocean based on high-quality inorganic carbon, alkalinity, chlorofluorocarbon, and nutrient data collected during the World Ocean Circulation Experiment (WOCE) Hydrographic Program, the Joint Global Ocean Flux Study (JGOFS), and the Ocean-Atmosphere Carbon Exchange Study (OACES) surveys of the Atlantic Ocean between 1990 and 1998. Anthropogenic CO_2 was separated from the large pool of dissolved inorganic carbon using an extended version of the ΔC* method originally developed by Gruber et al. [1996]. The extension of the method includes the use of an optimum multiparameter analysis to determine the relative contributions from various source water types to the sample on an isopycnal surface. Total inventories of anthropogenic CO_2 in the Atlantic Ocean are highest in the subtropical regions at 20°–40°, whereas anthropogenic CO_2 penetrates the deepest in high-latitude regions (>40°N). The deeper penetration at high northern latitudes is largely due to the formation of deep water that feeds the Deep Western Boundary Current, which transports anthropogenic CO_2 into the interior. In contrast, waters south of 50°S in the Southern Ocean contain little anthropogenic CO_2. Analysis of the data collected during the 1990–1998 period yielded a total anthropogenic CO_2 inventory of 28.4 ± 4.7 Pg C in the North Atlantic (equator-70°N) and of 18.5 ± 3.9 Pg C in the South Atlantic (equator-70°S). These estimated basin-wide inventories of anthropogenic CO_2 are in good agreement with previous estimates obtained by Gruber [1998], after accounting for the difference in observational periods. Our calculation of the anthropogenic CO_2 inventory in the Atlantic Ocean, in conjunction with the inventories calculated previously for the Indian Ocean [Sabine et al., 1999] and for the Pacific Ocean [Sabine et al., 2002], yields a global anthropogenic CO_2 inventory of 112 ± 17 Pg C that has accumulated in the world oceans during the industrial era. This global oceanic uptake accounts for approximately 29% of the total CO_2 emissions from the burning of fossil fuels, land-use changes, and cement production during the past 250 years.
机译:[1]本文根据世界海洋环流实验(WOCE)水文计划中收集的高质量无机碳,碱度,氯氟烃和营养数据,对大西洋沿岸全人类源CO_2清单进行了全面分析,在1990年至1998年期间进行了全球海洋通量联合研究(JGOFS)和大西洋的海洋-大气碳交换研究(OACES)调查。使用扩展的ΔC方法,从大量溶解的无机碳中分离出了人为的CO_2 *由Gruber等人最初开发的方法。 [1996]。该方法的扩展包括使用最佳多参数分析来确定各种水源水对等温面样品的相对贡献。在20°–40°的亚热带地区,大西洋的人为CO_2总库存量最高,而在高纬度地区(> 40°N),人为CO_2的渗透量最深。在北部高纬度地区更深的渗透主要是由于形成了深水,该水为深部西部边界水流输送,将人为的CO_2输送到内部。相反,南大洋南纬50°S以南的水几乎没有人为的CO_2。对1990-1998年期间收集的数据进行分析后,北大西洋(赤道70°N)和南大西洋(赤道70°)的人为CO_2总库存为28.4±4.7 Pg C,南大西洋为18.5±3.9 PgC。 S)。在考虑了观测期的差异之后,这些估计的全盆地人为CO_2清单与Gruber [1998]先前的估计非常吻合。我们对大西洋人为CO_2清单的计算,再加上先前针对印度洋[Sabine等,1999]和太平洋[Sabine等,2002]的清单,得出了全球人为CO_2工业时代在世界海洋中积累的112±17 Pg C清单。在过去250年中,全球海洋吸收量约占化石燃料燃烧,土地用途变化和水泥生产中CO_2排放总量的29%。

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