Ministry of Education Laboratory of Earth Surface Process, College of Urban and Environmental Sciences, Peking University, Beijing 100871, China; Key Laboratory of Geographic Information Science (Ministry of Education), East China Normal University, Shanghai 200241, China; School of Geographic Sciences, East China Normal University, Shanghai 200241, China.
School of Environment and Natural Resources, Renmin University of China, Beijing 100872, China.
Sci Total Environ. 2018 Jan 1;610-611:24-31. doi: 10.1016/j.scitotenv.2017.07.182. Epub 2017 Aug 9.
Growing concern about the risk associated with increasing environmental mercury (Hg) concentrations has resulted in a focus on the relationships between intercontinental emitted and accumulated Hg. We use a global biogeochemical Hg model with 8 continental regions and a global ocean to evaluate the legacy impacts of historical anthropogenic releases (2000BCE to 2008AD) on global source-receptor relationships of Hg. Legacy impacts of historical anthropogenic releases are confirmed to be significant on the source-receptor relationships according to our results. Historical anthropogenic releases from Asia account for 8% of total soil Hg in North America, which is smaller than the proportion (~17%) from previous studies. The largest contributors to the global oceanic Hg are historical anthropogenic releases from North America (26%), Asia (16%), Europe (14%) and South America (14%). Although anthropogenic releases from Asia have exceeded North America since the 1970s, source contributions to global Hg receptors from Asia have not exceeded North America so far. Future projections indicate that if Hg emissions are not effectively controlled, Asia will exceed North America as the largest contributor to the global ocean in 2019 and this has a long-term adverse impact on the future environment. For the Arctic Ocean, historical anthropogenic release from North America contributes most to the oceanic Hg reservoir and future projections reveal that the legacy impacts of historical releases from mid-latitudes would lead to the potential of rising Hg in the Arctic Ocean in the future decades, which calls for more effective Hg controls on mid-latitude releases.
对与不断增加的环境汞(Hg)浓度相关的风险的日益关注,促使人们关注洲际排放和积累的 Hg 之间的关系。我们使用具有 8 个大陆区域和一个全球海洋的全球生物地球化学 Hg 模型,评估历史人为排放(公元前 2000 年至 2008 年)对 Hg 的全球源-汇关系的遗留影响。根据我们的结果,历史人为排放的遗留影响被确认对源-汇关系具有重要影响。历史人为排放的 Hg 中,亚洲的排放占北美的土壤总 Hg 的 8%,小于之前研究中的比例(~17%)。对全球海洋 Hg 贡献最大的是北美(26%)、亚洲(16%)、欧洲(14%)和南美洲(14%)的历史人为排放。尽管自 20 世纪 70 年代以来,亚洲的人为排放已经超过了北美,但到目前为止,亚洲对全球 Hg 受体的源贡献尚未超过北美。未来预测表明,如果 Hg 排放得不到有效控制,亚洲将在 2019 年超过北美,成为全球海洋的最大贡献者,这对未来环境将产生长期不利影响。对于北冰洋,北美历史人为排放对海洋 Hg 库的贡献最大,未来预测显示,中纬度历史排放的遗留影响将导致未来几十年北冰洋 Hg 含量上升的可能性,这需要对中纬度排放进行更有效的 Hg 控制。