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Rise to modern levels of ocean oxygenation coincided with the Cambrian radiation of animals.海洋氧合作用上升到现代水平与动物的寒武纪辐射同时发生。
Nat Commun. 2015 May 18;6:7142. doi: 10.1038/ncomms8142.
2
Uranium isotopes distinguish two geochemically distinct stages during the later Cambrian SPICE event.铀同位素区分了寒武纪晚期“香料”事件期间两个地球化学性质不同的阶段。
Earth Planet Sci Lett. 2014 Sep 1;401:313-326. doi: 10.1016/j.epsl.2014.05.043.
3
Isotopic constraints on biogeochemical cycling of copper in the ocean.海洋中铜的生物地球化学循环的同位素制约。
Nat Commun. 2014 Dec 5;5:5663. doi: 10.1038/ncomms6663.
4
Quantification of dissolved iron sources to the North Atlantic Ocean.量化进入北大西洋的溶解态铁源。
Nature. 2014 Jul 10;511(7508):212-5. doi: 10.1038/nature13482. Epub 2014 Jul 2.
5
Stable isotope ratio measurements of Cu and Zn in mineral dust (bulk and size fractions) from the Taklimakan Desert and the Sahel and in aerosols from the eastern tropical North Atlantic Ocean.对来自塔克拉玛干沙漠和萨赫勒地区的矿物尘(整体和粒径分级)以及来自东北大西洋东部的气溶胶中的铜和锌的稳定同位素比值进行测量。
Talanta. 2013 Sep 30;114:103-9. doi: 10.1016/j.talanta.2013.03.062. Epub 2013 Apr 2.
6
A new method for precise determination of iron, zinc and cadmium stable isotope ratios in seawater by double-spike mass spectrometry.双带同位素稀释质谱法精确测定海水中铁、锌和镉稳定同位素比值的新方法。
Anal Chim Acta. 2013 Sep 2;793:44-52. doi: 10.1016/j.aca.2013.07.025. Epub 2013 Jul 15.
7
Determination of isotopic composition of dissolved copper in seawater by multi-collector inductively coupled plasma mass spectrometry after pre-concentration using an ethylenediaminetriacetic acid chelating resin.采用乙二胺四乙酸螯合树脂预富集,多接收电感耦合等离子体质谱法测定海水中溶解态铜的同位素组成。
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8
A Zn isotope perspective on the rise of continents.从锌同位素角度看大陆的崛起。
Geobiology. 2013 May;11(3):201-14. doi: 10.1111/gbi.12030. Epub 2013 Feb 20.
9
Zinc isotopic fractionation: why organic matters.锌同位素分馏:为何是有机物。
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10
A biomarker based on the stable isotopes of nickel.一种基于镍稳定同位素的生物标志物。
Proc Natl Acad Sci U S A. 2009 Jul 7;106(27):10944-8. doi: 10.1073/pnas.0900726106. Epub 2009 Jun 24.

镍和锌同位素的海洋收支:以黑海为例说明硫化环境的重要性。

The oceanic budgets of nickel and zinc isotopes: the importance of sulfidic environments as illustrated by the Black Sea.

作者信息

Vance Derek, Little Susan H, Archer Corey, Cameron Vyllinniskii, Andersen Morten B, Rijkenberg Micha J A, Lyons Timothy W

机构信息

Institute of Geochemistry and Petrology, Department of Earth Sciences, ETH Zürich, Clausiusstrasse 25, 8092 Zürich, Switzerland

Institute of Geochemistry and Petrology, Department of Earth Sciences, ETH Zürich, Clausiusstrasse 25, 8092 Zürich, Switzerland.

出版信息

Philos Trans A Math Phys Eng Sci. 2016 Nov 28;374(2081). doi: 10.1098/rsta.2015.0294.

DOI:10.1098/rsta.2015.0294
PMID:29035259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5069529/
Abstract

Isotopic data collected to date as part of the GEOTRACES and other programmes show that the oceanic dissolved pool is isotopically heavy relative to the inputs for zinc (Zn) and nickel (Ni). All Zn sinks measured until recently, and the only output yet measured for Ni, are isotopically heavier than the dissolved pool. This would require either a non-steady-state ocean or other unidentified sinks. Recently, isotopically light Zn has been measured in organic carbon-rich sediments from productive upwelling margins, providing a potential resolution of this issue, at least for Zn. However, the origin of the isotopically light sedimentary Zn signal is uncertain. Cellular uptake of isotopically light Zn followed by transfer to sediment does not appear to be a quantitatively important process. Here, we present Zn and Ni isotope data for the water column and sediments of the Black Sea. These data demonstrate that isotopically light Zn and Ni are extracted from the water column, probably through an equilibrium fractionation between different dissolved species followed by sequestration of light Zn and Ni in sulfide species to particulates and the sediment. We suggest that a similar, non-quantitative, process, operating in porewaters, explains the Zn data from organic carbon-rich sediments.This article is part of the themed issue 'Biological and climatic impacts of ocean trace element chemistry'.

摘要

作为全球海洋微量元素研究计划(GEOTRACES)及其他项目的一部分,迄今收集的同位素数据表明,相对于锌(Zn)和镍(Ni)的输入而言,海洋溶解态库的同位素偏重。直到最近测量的所有锌汇,以及目前唯一测量到的镍输出,其同位素都比溶解态库偏重。这将需要一个非稳态海洋或其他未明确的汇。最近,在生产力较高的上升流边缘富含有机碳的沉积物中测量到了同位素偏轻的锌,这至少为锌的这一问题提供了一种可能的解决方案。然而,同位素偏轻的沉积锌信号的来源尚不确定。细胞摄取同位素偏轻的锌然后转移到沉积物中,似乎不是一个数量上重要的过程。在此,我们展示了黑海水柱和沉积物的锌和镍同位素数据。这些数据表明,同位素偏轻的锌和镍是从水柱中提取的,可能是通过不同溶解态物种之间的平衡分馏,然后轻锌和镍在硫化物物种中被螯合到颗粒物和沉积物中。我们认为,在孔隙水中发生的类似但非定量的过程,可以解释富含有机碳沉积物中的锌数据。本文是主题为“海洋微量元素化学的生物和气候影响”特刊的一部分。