巴西雅卡迪戈组铁矿沉积过程中的地表水含氧量和低生物生产率:镉-铬同位素组合的启示

IF 3.6 2区 地球科学 Q1 GEOCHEMISTRY & GEOPHYSICS Chemical Geology Pub Date : 2024-04-25 DOI:10.1016/j.chemgeo.2024.122101
Robert Frei , Claudio Gaucher , Paulo César Boggiani , Jesper Allan Frederiksen , Samantha Renee Walker , Henrique Albuquerque Fernandes , Fabricio Caxito
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引用次数: 0

摘要

班达阿尔塔地层(巴西南马托格罗索州乌鲁库姆区)由∼600 Ma铁和锰矿床组成,是世界上最年轻、最大的新新生代沉积铁和锰地层(IF;MnF)之一。这些矿床沉积在一个氧化还原分层的海洋次盆地(Jacadigo 盆地)中,该盆地受到冰川前进/后退周期的强烈影响,大陆淡水暂时流入,富含金属的深层缺氧海水上涌。从钻探岩芯样本中精心分离的赤铁矿介带上测量到的铬和镉同位素在整个约 325 米厚的取样序列中相对均匀。在班达阿尔塔地层取样的 325 米厚层序中,自生δ53Cr 平均值为 +0.93 ± 0.24 ‰(2σ;n = 23),δ114Cd 平均值为 -0.14 ± 0.14 ‰(2σ;n = 15)。铬的显著富集与其他氧化还原敏感元素(铀、钼)的强烈富集并存,证明了在周期性冰川退缩阶段,富含 Fe2+ 的上涌水体到达暴露于大气的含氧表层时,表层水体中有效和高效的还原去除过程。假定铁氧氢氧化物对溶解镉具有类似的定量和高效去除途径,那么推断出的雅卡迪戈盆地表层水平均δ114Cd特征值为-0.14 ± 0.14 ‰,明显低于现代海洋表层水的特征值(δ114Cd范围约为∼0.4至∼1 ‰),甚至低于现代海洋深层水的特征值(δ114Cd范围为∼0.3 ‰)。这可能证明,与今天相比,新近纪晚期雅卡迪戈组沉积过程中初级生产水平降低,营养物质利用率降低。尽管推断这一时期的地表水层一定是氧化的,但赤铁矿介带所显示的类似海水的、页岩归一化稀土元素和钇(REY)模式中记录的强正分馏铬同位素特征和明显的负铈异常都暗示了这一点。本文提供的数据说明(1)沉积时,稳定的同位素重铬输入到雅卡迪戈盆地,这意味着新近纪晚期大气中的氧气水平较高,(2)溶解的铬和镉可能分别定量地还原融入/吸附到沉淀的铁氧氢氧化物中,以及(3)在冰川退缩周期中,雅卡迪戈盆地的营养物质浓度和利用率普遍较低。带状铁地层被认为是重建过去海洋沉积盆地(包括新近纪冰川条件下的沉积盆地)氧化还原和生物生产率水平的合适档案,方法是采用铬镉同位素双示踪剂对富铁介带进行示踪。
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Surface water oxygenation and low bioproductivity during deposition of iron formation of the Jacadigo Group (Brazil): Insights from combined cadmium – Chromium isotopes

The Banda Alta Formation (Urucum district, Mato Grosso do Sul, Brazil) comprises ∼600 Ma Fe and Mn deposits, which are among the world's youngest and largest Neoproterozoic sedimentary Fe and Mn formations (IF; MnF). These have been deposited in a redox-stratified, marine sub-basin (Jacadigo Basin), which was strongly influenced by glacial advance/retraction cycles with temporary influx of continental freshwater and upwelling of metal-enriched deep anoxic seawater. Cr and Cd isotopes measured on meticulously separated hematite mesobands from drill core samples are relatively homogenous throughout the ca. 325 m thick sequence sampled in the Banda Alta Fm., with average authigenic δ53Cr values of +0.93 ± 0.24 ‰ (2σ; n = 23) and δ114Cd values of −0.14 ± 0.14 ‰ (2σ; n = 15). The significant enrichment of Cr, in parallel with the strong enrichments of other redox sensitive elements (U, Mo), attests for effective and efficient reduction removal processes in the surface waters during cycles where upwelling Fe2+-rich waters reached the oxygenated surface layer exposed to the atmosphere during episodic glacier retreat stages. Assuming a similar quantitative and efficient removal pathway of dissolved Cd by iron oxyhydroxides, the so-inferred average δ114Cd signature of −0.14 ± 0.14 ‰ in the Jacadigo Basin surface water is significantly lower than signatures of modern ocean surface waters with a range of δ114Cd of ca. ∼0.4 to ∼1 ‰ and even lower than the signature of modern ocean deep waters with δ114Cd of ∼0.3 ‰. It possibly attests to reduced primary production levels and lower nutrient utilization rates during deposition of the Late Neoproterozoic Jacadigo Group, compared to today. This despite the inferred oxidized surface water layer that must have prevailed during this time, as implied by the strongly positively fractionated Cr isotope signatures and pronouncedly negative Ce-anomalies recorded in the seawater-like, shale-normalized Rare Earth Element and Yttrium (REY) patterns exhibited by the hematite mesobands. Data presented herein speak for: (1) a stable, isotopically heavy Cr input to the Jacadigo Basin at the time of deposition, implying high atmospheric O2 levels in the Late Neoproterozoic (2) likely quantitative, reductive incorporation / adsorption processes of dissolved Cr and Cd, respectively, into/onto precipitating iron oxyhydroxides, and (3) the prevalence of low nutrient concentrations and utilization rates in the Jacadigo Basin during glacier retreat cycles. Banded iron formations are considered suitable archives for reconstructing redox and bioproductivity levels in past marine depositional basin, including those prevalent in Neoproterozoic glacial conditions, via employing the CrCd isotope double tracer to iron-rich mesobands.

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来源期刊
Chemical Geology
Chemical Geology 地学-地球化学与地球物理
CiteScore
7.20
自引率
10.30%
发文量
374
审稿时长
3.6 months
期刊介绍: Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry. The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry. Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry. The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.
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