The distribution of lead concentrations and isotope compositions in the eastern Tropical Atlantic Ocean

被引:23
|
作者
Bridgestock, Luke [1 ]
Rehkaemper, Mark [1 ]
van de Flierdt, Tina [1 ]
Paul, Maxence [1 ]
Milne, Angela [2 ]
Lohan, Maeve C. [3 ]
Achterberg, Eric P. [4 ]
机构
[1] Imperial Coll London, Dept Earth Sci & Engn, London SW7 2AZ, England
[2] Univ Plymouth, Sch Geog Earth & Environm Sci, Plymouth PL4 8AA, Devon, England
[3] Univ Southampton, Natl Oceanog Ctr Southampton, Ocean & Earth Sci, Southampton SO14 3ZH, Hants, England
[4] GEOMARHelmholtz Ctr Ocean Res, D-24148 Kiel, Germany
关键词
Anthropogenic Pb; Pb isotopes; Transient tracers; Ocean circulation; WESTERN NORTH-ATLANTIC; ANTHROPOGENIC LEAD; WATER MASSES; PB-ISOTOPES; CIRCULATION; SECTION; RECORD; RECONSTRUCTION; CONTAMINATION; VARIABILITY;
D O I
10.1016/j.gca.2018.01.018
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Anthropogenic emissions have dominated marine Pb sources during the past century. Here we present Pb concentrations and isotope compositions for ocean depth profiles collected in the eastern Tropical Atlantic Ocean (GEOTRACES section GA06), to trace the transfer of anthropogenic Pb into the ocean interior. Variations in Pb concentration and isotope composition were associated with changes in hydrography. Water masses ventilated in the southern hemisphere generally featured lower Pb-206/Pb-207 and Pb-208/Pb-207 ratios than those ventilated in the northern hemisphere, in accordance with Pb isotope data of historic anthropogenic Pb emissions. The distributions of Pb concentrations and isotope compositions in northern sourced waters were consistent with differences in their ventilation timescales. For example, a Pb concentration maximum at intermediate depth (600-900 m, 35 pmol kg(-1)) in waters sourced from the Irminger/Labrador Seas, is associated with Pb isotope compositions (Pb-206/Pb-207 = 1.1818-1.1824, Pb-208/Pb-207 = 2.4472-2.4483) indicative of northern hemispheric emissions during the 1950s and 1960s close to peak leaded petrol usage, and a transit time of similar to 50-60 years. In contrast, North Atlantic Deep Water (2000-4000 m water depth) featured lower Pb concentrations and isotope compositions (Pb-206/Pb-207 = 1.176 2-1.184, Pb-208/Pb-207 = 2.4482-2.4545) indicative of northern hemispheric emissions during the 1910s and 1930s and a transit time of similar to 80-100 years. This supports the notion that transient anthropogenic Pb inputs are predominantly transferred into the ocean interior by water mass transport. However, the interpretation of Pb concentration and isotope composition distributions in terms of ventilation timescales and pathways is complicated by (1) the chemical reactivity of Pb in the ocean, and (2) mixing of waters ventilated during different time periods. The complex effects of water mass mixing on Pb distributions is particularly apparent in seawater in the Tropical Atlantic Ocean which is ventilated from the southern hemisphere. In particular, South Atlantic Central Water and Antarctic Intermediate Water were dominated by anthropogenic Pb emitted during the last 50-100 years, despite estimates of much older average ventilation ages in this region. (C) 2018 The Author(s). Published by Elsevier Ltd.
引用
收藏
页码:36 / 51
页数:16
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