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海平面对埃迪卡拉纪-寒武纪动物辐射的控制。

Sea level controls on Ediacaran-Cambrian animal radiations.

机构信息

School of GeoSciences, University of Edinburgh, James Hutton Road, Edinburgh EH9 3FE, UK.

出版信息

Sci Adv. 2024 Aug 2;10(31):eado6462. doi: 10.1126/sciadv.ado6462. Epub 2024 Jul 31.

DOI:10.1126/sciadv.ado6462
PMID:39083611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11290527/
Abstract

The drivers of Ediacaran-Cambrian metazoan radiations remain unclear, as does the fidelity of the record. We use a global age framework [580-510 million years (Ma) ago] to estimate changes in marine sedimentary rock volume and area, reconstructed biodiversity (mean genus richness), and sampling intensity, integrated with carbonate carbon isotopes (δC) and global redox data [carbonate Uranium isotopes (δU)]. Sampling intensity correlates with overall mean reconstructed biodiversity >535 Ma ago, while second-order (~10-80 Ma) global transgressive-regressive cycles controlled the distribution of different marine sedimentary rocks. The temporal distribution of the Avalon assemblage is partly controlled by the temporally and spatially limited record of deep-marine siliciclastic rocks. Each successive rise of metazoan morphogroups that define the Avalon, White Sea, and Cambrian assemblages appears to coincide with global shallow marine oxygenation events at δC maxima, which precede major sea level transgressions. While the record of biodiversity is biased, early metazoan radiations and oxygenation events are linked to major sea level cycles.

摘要

埃迪卡拉纪-寒武纪后生动物辐射的驱动因素仍不清楚,记录的保真度也是如此。我们使用全球年龄框架[5.8 亿至 5.1 亿年前]来估计海洋沉积岩体积和面积的变化、重建生物多样性(平均属丰富度)和采样强度,同时结合碳酸盐碳同位素(δC)和全球氧化还原数据[碳酸盐铀同位素(δU)]。采样强度与整体平均重建生物多样性相关>5.35 亿年前,而二级(~10-80 百万年)全球海进-海退旋回控制着不同海洋沉积岩的分布。阿瓦隆组合的时间分布部分受深海硅质碎屑岩记录的时间和空间限制的控制。定义阿瓦隆、白海和寒武纪组合的后生动物形态群的每一次连续上升似乎都与 δC 最大值处的全球浅海氧化事件同时发生,而这些事件发生在前海的主要海平面上升之前。尽管生物多样性的记录存在偏差,但早期后生动物辐射和氧化事件与主要的海平面周期有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/08ac4768cce9/sciadv.ado6462-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/36d51db2c2c6/sciadv.ado6462-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/dd9e7d454615/sciadv.ado6462-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/d80c0c422f60/sciadv.ado6462-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/fb954966ddb6/sciadv.ado6462-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/08ac4768cce9/sciadv.ado6462-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/36d51db2c2c6/sciadv.ado6462-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/a05eea308936/sciadv.ado6462-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/dc2c6f5fae50/sciadv.ado6462-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/dd9e7d454615/sciadv.ado6462-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/d80c0c422f60/sciadv.ado6462-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/fb954966ddb6/sciadv.ado6462-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d487/11290527/08ac4768cce9/sciadv.ado6462-f7.jpg

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