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以皮克数量级分辨率追踪单个颗石藻的溶解及其对二氧化碳封存和海洋酸化的影响。

Tracking single coccolith dissolution with picogram resolution and implications for CO2 sequestration and ocean acidification.

机构信息

Department of Chemistry, Nano-Science Center, University of Copenhagen, 2100 Copenhagen, Denmark.

出版信息

Proc Natl Acad Sci U S A. 2011 May 24;108(21):8571-6. doi: 10.1073/pnas.1009447108. Epub 2011 May 6.

DOI:10.1073/pnas.1009447108
PMID:21551094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3102388/
Abstract

Coccoliths are micrometer scale shields made from 20 to 60 individual calcite (CaCO(3)) crystals that are produced by some species of algae. Currently, coccoliths serve as an important sink in the global carbon cycle, but decreasing ocean pH challenges their stability. Chalk deposits, the fossil remains of ancient algae, have remained remarkably unchanged by diagenesis, the process that converts sediment to rock. Even after 60 million years, the fossil coccolith crystals are still tiny (< 1 μm), compared with inorganically produced calcite, where one day old crystals can be 10 times larger, which raises the question if the biogenic nature of coccolith calcite gives it different properties than inorganic calcite? And if so, can these properties protect coccoliths in CO(2) challenged oceans? Here we describe a new method for tracking dissolution of individual specimens, at picogram (10(-12) g) resolution. The results show that the behavior of modern and fossil coccoliths is similar and both are more stable than inorganic calcite. Organic material associated with the biogenic calcite provides the explanation. However, ancient and modern coccoliths, that resist dissolution in Ca-free artificial seawater at pH > 8, all dissolve when pH is 7.8 or lower. Ocean pH is predicted to fall below 7.8 by the year 2100, in response to rising CO(2) levels. Our results imply that at these conditions the advantages offered by the biogenic nature of calcite will disappear putting coccoliths on algae and in the calcareous bottom sediments at risk.

摘要

球石是由 20 到 60 个单独的方解石(CaCO(3))晶体组成的微米级盾牌,由一些藻类物种产生。目前,球石是全球碳循环中的一个重要汇,但海洋 pH 值的降低挑战了它们的稳定性。白垩沉积物是古代藻类的化石遗迹,经过成岩作用(将沉积物转化为岩石的过程)后仍然保持着惊人的不变。即使经过 6000 万年,化石球石晶体仍然很小(<1μm),与无机方解石相比,一天大的晶体可以大 10 倍,这就提出了一个问题,即球石方解石的生物成因是否赋予了它与无机方解石不同的性质?如果是这样,这些特性是否能保护球石免受 CO(2)挑战的海洋的影响?在这里,我们描述了一种新的方法,可以在皮克微克(10(-12)g)分辨率下跟踪单个标本的溶解情况。结果表明,现代和化石球石的行为相似,两者都比无机方解石更稳定。与生物成因方解石相关的有机物质提供了答案。然而,在 pH 值大于 8 的无钙人工海水中抵抗溶解的古代和现代球石,当 pH 值为 7.8 或更低时都会溶解。预计到 2100 年,海洋 pH 值将下降到 7.8 以下,以应对 CO(2)水平的上升。我们的研究结果表明,在这些条件下,方解石的生物成因所带来的优势将消失,这使得球石及其所在的藻类和钙质底泥处于危险之中。