Controls on boron incorporation in cultured tests of the planktic foraminifer Orbulina universa

被引:72
作者
Allen, Katherine A. [1 ]
Hoenisch, Baerbel [1 ]
Eggins, Stephen M. [2 ]
Yu, Jimin [1 ]
Spero, Howard J. [3 ]
Elderfield, Henry [4 ]
机构
[1] Columbia Univ, Lamont Doherty Earth Observ, Palisades, NY 10964 USA
[2] Australian Natl Univ, Res Sch Earth Sci, Canberra, ACT, Australia
[3] Univ Calif Davis, Dept Geol, Davis, CA 95616 USA
[4] Univ Cambridge, Dept Earth Sci, Cambridge CB2 3EQ, England
基金
美国国家科学基金会; 澳大利亚研究理事会;
关键词
boron; seawater carbonate system; pH proxy; Orbulina universa; planktic foraminifera; SEAWATER CARBONATE CONCENTRATION; ISOTOPIC COMPOSITION; GLOBIGERINOIDES-SACCULIFER; SYMBIONT PHOTOSYNTHESIS; CALCITE PRECIPITATION; HUMIC ACIDS; BORIC-ACID; PH CONTROL; OCEAN; MODEL;
D O I
10.1016/j.epsl.2011.07.010
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
070403 [天体物理学]; 070902 [地球化学];
摘要
Culture experiments with living planktic foraminifers reveal that the ratio of boron to calcium (B/Ca) in Orbulina universa increases from 56 to 92 mu mol mol(-1) when pH is raised from 7.61 +/-0.02 to 8.67 +/-0.03 (total scale). Across this pH range, the abundances of carbonate, bicarbonate, and borate ions also change ( + 530, -500, and + 170 mu mol kg(-1), respectively). Thus specific carbonate system control(s) on B/Ca remain unclear, complicating interpretation of paleorecords. B/Ca in cultured O. universa also increases with salinity (55-72 mu mol mol(-1) from 29.9-35.4 parts per thousand) and seawater boron concentration (62-899 mu mol mol(-1) from 4-40 ppm B), suggesting that these parameters may need to be taken into account for paleorecords spanning large salinity changes (similar to 2 parts per thousand) and for samples grown in seawater whose boron concentration ([B](SW)) differs from modern by more than 0.25 ppm. While our results are consistent with the predominant incorporation of the charged borate species B(OH)(4) - into foraminiferal calcite, the behavior of the partition coefficient K-D. (defined as [B/Ca](calcite)/[B(OH)(4)- / HCO3-](seawater)) cannot be explained by borate incorporation alone, and suggests the involvement of other pH-sensitive ions such as CO32- For a given increase in seawater B(OH)(4) -, the corresponding increase in B/Ca is stronger when B(OH)(4) - is raised by increasing [B](sw) than when it is raised by increasing pH. These results suggest that B incorporation controls should be reconsidered. Additional insight is gained from laser-ablation ICP-MS profiles, which reveal variable B/Ca distributions within individual shells. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:291 / 301
页数:11
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