Li C, Hardisty D S, Luo G, Huang J, Algeo T J, Cheng M, Shi W, An Z, Tong J, Xie S, Jiao N, Lyons T W
State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences, Wuhan, China.
Department of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA, USA.
Geobiology. 2017 Mar;15(2):211-224. doi: 10.1111/gbi.12222. Epub 2016 Dec 20.
Records of the Ediacaran carbon cycle (635-541 million years ago) include the Shuram excursion (SE), the largest negative carbonate carbon isotope excursion in Earth history (down to -12‰). The nature of this excursion remains enigmatic given the difficulties of interpreting a perceived extreme global decrease in the δ C of seawater dissolved inorganic carbon. Here, we present carbonate and organic carbon isotope (δ C and δ C ) records from the Ediacaran Doushantuo Formation along a proximal-to-distal transect across the Yangtze Platform of South China as a test of the spatial variation of the SE. Contrary to expectations, our results show that the magnitude and morphology of this excursion and its relationship with coexisting δ C are highly heterogeneous across the platform. Integrated geochemical, mineralogical, petrographic, and stratigraphic evidence indicates that the SE is a primary marine signature. Data compilations demonstrate that the SE was also accompanied globally by parallel negative shifts of δ S of carbonate-associated sulfate (CAS) and increased Sr/ Sr ratio and coastal CAS concentration, suggesting elevated continental weathering and coastal marine sulfate concentration during the SE. In light of these observations, we propose a heterogeneous oxidation model to explain the high spatial heterogeneity of the SE and coexisting δ C records of the Doushantuo, with likely relevance to the SE in other regions. In this model, we infer continued marine redox stratification through the SE but with increased availability of oxidants (e.g., O and sulfate) limited to marginal near-surface marine environments. Oxidation of limited spatiotemporal extent provides a mechanism to drive heterogeneous oxidation of subsurface reduced carbon mostly in shelf areas. Regardless of the mechanism driving the SE, future models must consider the evidence for spatial heterogeneity in δ C presented in this study.
埃迪卡拉纪碳循环(6.35亿至5.41亿年前)的记录包括舒拉姆偏移(SE),这是地球历史上最大的负碳酸盐碳同位素偏移(低至-12‰)。鉴于解释海水溶解无机碳δC明显的全球极端下降存在困难,这次偏移的性质仍然成谜。在此,我们展示了沿中国南方扬子地台从近岸到远岸剖面的埃迪卡拉纪陡山沱组碳酸盐和有机碳同位素(δC和δC)记录,以此检验SE的空间变化。与预期相反,我们的结果表明,这次偏移的幅度和形态及其与共存δC的关系在整个地台上高度不均一。综合地球化学、矿物学、岩石学和地层学证据表明,SE是一种主要的海洋特征。数据汇编显示,全球范围内SE还伴随着碳酸盐相关硫酸盐(CAS)的δS平行负向变化、87Sr/86Sr比值增加以及沿海CAS浓度升高,这表明在SE期间大陆风化增强,沿海海洋硫酸盐浓度增加。鉴于这些观察结果,我们提出了一个非均质氧化模型来解释陡山沱组SE和共存δC记录的高空间非均一性,这可能与其他地区的SE相关。在这个模型中,我们推断在整个SE期间海洋氧化还原分层持续存在,但氧化剂(如O和硫酸盐)的可用性增加仅限于近岸浅海边缘环境。有限时空范围内的氧化提供了一种机制,主要在陆架区域驱动地下还原碳的非均质氧化。无论驱动SE的机制如何,未来的模型都必须考虑本研究中提出的δC空间非均一性的证据。