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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Chromium isotope cycling in the water column and sediments of the Peruvian continental margin
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Chromium isotope cycling in the water column and sediments of the Peruvian continental margin

机译:铬同位素在水柱中循环和秘鲁大陆边缘的沉积物

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Chromium (Cr) isotope fractionation is sensitive to redox changes and the Cr isotopic composition (delta Cr-53) of sedimentary rocks has been used to reconstruct marine redox conditions and atmospheric oxygenation in the past. However, little is known about the behaviour of chromium isotopes across modern marine redox boundaries. We investigated Cr concentrations and delta Cr-53 variations in seawater and sediment across the Peruvian oxygen minimum zone (OMZ) to provide a better understanding of Cr cycling in the ocean. We found that seawater delta Cr-53 values ranged from 0.02 +/- 0.16 parts per thousand to 0.59 +/- 0.11 parts per thousand (2SD) and sediment values from 0.31 +/- 0.07 to 0.92 +/- 0.12 parts per thousand. Neither Cr concentrations nor delta Cr-53 values in the water column revealed significant shifts across the oxic-anoxic boundaries. Instead, processes that operate at a local scale, such as Cr scavenging by Fe-rich particles and Cr release from reducing sediments, are identified as the main controls on Cr concentrations and isotope compositions in the water column. The delta Cr-53 values of sediments deposited in permanently anoxic waters (0.77 +/- 0.19 parts per thousand, n = 5) are significantly different from the delta Cr-53 values of sediments deposited in oxic bottom waters (0.46 +/- 0.19 parts per thousand, n = 4). This suggests that sediment Cr concentrations and delta Cr-53 values are to some extent influenced by water column redox (e.g. reductive dissolution and transport of Fe oxides) and/or early diagenetic (e.g. redistribution of Cr during phosphogenesis) processes as well as biologic activity. Our data demonstrate that local scale water column redox gradients and sediment exchange can lead to a large range of delta Cr-53 values in sediments, comparable to the range found in the entire geologic record to date. Given the increasing prominence of Cr isotope measurements in constraining atmospheric oxygenation in deep time, we argue that th
机译:铬(Cr)同位素分馏对氧化还原变化敏感,沉积岩的Cr同位素组合物(Delta Cr-53)已被用于重建过去的海洋氧化还原条件和大气氧合。然而,对现代海洋氧化还原界限的铬同位素的行为知之甚少。我们研究了CR浓度和Delta CR-53在秘鲁氧气最小区域(OMZ)上的海水和沉积物的变化,以更好地了解海洋中的Cr循环。我们发现海水Delta CR-53值范围从0.02 +/- 0.16份,0.59 +/- 0.11份,0.31 +/- 0.07至0.92 +/- 0.12零件0.92 + 0.12份。水柱中的Cr浓度和ΔCr-53值都没有显示出氧缺氧边界的显着变化。相反,以局部规模操作的方法,例如通过Fe-Rich颗粒和Cr释放从还原沉积物中的Cr清除,被鉴定为水柱中Cr浓度和同位素组合物的主要对照。沉积在永久性缺氧水处(0.77 +/- 0.19份,N = 5)中沉积的沉积物的值与沉积在氧底部水中的沉积物的Delta Cr-53值显着不同(0.46 +/- 0.19百分之一,n = 4)。这表明沉积物Cr浓度和δCr-53值在一定程度上受水柱氧化还原的影响(例如还原溶解和Fe氧化物的运输)和/或早期成岩(例如,磷酸过程中Cr的再分布)过程以及生物活性。我们的数据表明,本地规模水柱氧化还原梯度和沉积物交换可以导致沉积物中的大量Delta Cr-53值,与迄今为止整个地质记录中的范围相当。鉴于Cr同位素测量的越来越突出,在深度时间内约束大气氧合,我们认为

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