Anthropogenic Zn contamination dispersion in Sepetiba Bay evidenced by Zn isotopes

Bruno C A Cunha, D. Araújo, J. Garnier, E. Dantas, M. Babinski, I. Ruiz, C. Souto-Oliveira, M. Geraldes, D. Rocha, W. Machado
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Abstract

Sedimentary processes in coastal environments play a key role in the spatial dispersion of metal contaminants, including Zn. Combining Zn stable isotope signatures (δ66Zn) with traditional proxies of sedimentary sources and dispersal and post-depositional processes is a promising approach to understanding Zn anthropogenic dynamics in coastal systems that remains untested. To this end, we coupled geochemical and isotope tools to infer sedimentary contributions on Zn fate and behavior in surface sediments of Sepetiba bay, a tropical lagoon in Rio de Janeiro state chronically contaminated by an old stake of electroplating wastes Zn-enrich. Our results show high variability in δ66Zn values (0.43‰ to 0.89‰) and Zn enrichment factors (1 to 23-fold), evidencing a gradient in mixing sedimentary sources. The biplot δ66Zn versus 1/[Zn] highlights that the Zn isotope variability of most samples fell within a mixing source trend involving natural Zn (+0.29‰, 67 mg.kg-1) and anthropogenic Zn (+0.89‰, 3,440 mg.kg-1), the latter attributed to the Sepetiba bay’s historical Zn metallurgical contamination. Based on the isotope mixing model and geochemical proxies (e.g., Ti/Al ratio), we calculated that Zn excess in the Sepetiba Bay varies from 42% to 98%. The Zn enrichment distribution across the bay confirmed anthropogenic Zn dispersal from the Saco de Engenho, mainly controlled by the clock direction water current. Sediments mineralogical composition and correlations between Zn isotope and Al concentrations indicate that the high content of anthropogenic Zn is associated with silt and clay sediment particles composed of gibbsite and clay minerals such as kaolinite and organic matter. Our findings demonstrate that combining Zn isotope ratios with other geochemical proxies may help pinpoint Zn anthropogenic origins and behavior as well as track its dispersion in the land-sea continuum. In this case, this approach provides more accurate results on Zn contamination dispersion in the Sepetiba Bay and avoids possible misleading interpretations concerning anthropogenic Zn origins at low Zn concentration levels.
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由锌同位素证明的Sepetiba湾人为锌污染扩散
沿海环境中的沉积过程在包括锌在内的金属污染物的空间扩散中起着关键作用。将锌稳定同位素特征(δ66Zn)与沉积源、扩散和沉积后过程的传统指标相结合,是了解沿海系统中锌人为动力学的一种很有前途的方法,但尚未经过测试。为此,我们结合地球化学和同位素工具,推断沉积对Sepetiba湾表层沉积物中锌命运和行为的贡献。Sepetiba海湾是里约热内卢州的一个热带泻湖,长期受到电镀废物富集锌的老桩污染。我们的结果显示,δ66Zn值(0.43‰至0.89‰)和Zn富集因子(1至23倍)具有很高的可变性,证明了混合沉积源的梯度。δ66Zn与1/[Zn]的双标图突出表明,大多数样品的Zn同位素变异性属于混合源趋势,包括天然Zn(+0.29‰,67 mg.kg-1)和人为Zn(+0.89‰,3440 mg.kg--1),后者归因于Sepetiba湾历史上的锌冶金污染。根据同位素混合模型和地球化学指标(如Ti/Al比),我们计算出Sepetiba湾的Zn过剩率在42%至98%之间。整个海湾的锌富集分布证实了人为的锌从萨科-德恩根霍扩散,主要受时钟方向水流的控制。沉积物的矿物学组成以及Zn同位素和Al浓度之间的相关性表明,高含量的人为Zn与由三水铝石和粘土矿物(如高岭石和有机物)组成的淤泥和粘土沉积物颗粒有关。我们的研究结果表明,将锌同位素比率与其他地球化学指标相结合,可能有助于确定锌的人为起源和行为,并追踪其在陆海连续体中的分布。在这种情况下,这种方法提供了关于Sepetiba湾锌污染扩散的更准确的结果,并避免了对低锌浓度水平下人为锌来源的可能误导性解释。
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审稿时长
16 weeks
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