Paul K Mareike, van Helmond Niels A G M, Slomp Caroline P, Jilbert Tom
Environmental Geochemistry Group, Department of Geography and Geosciences, Faculty of Science, University of Helsinki, Helsinki, P.O 64 (Gustaf Hällströmin katu 2), FI-00014, Finland.
Department of Earth Sciences, Faculty of Geosciences, Utrecht University, Utrecht 3584 CB, the Netherlands; Radboud Institute for Biological and Environmental Sciences, Faculty of Science, Radboud University, Nijmegen 6525 AJ, the Netherlands.
Sci Total Environ. 2024 Nov 15;951:175789. doi: 10.1016/j.scitotenv.2024.175789. Epub 2024 Aug 26.
Rapidly spreading industrialization since the 19th century has led to a drastic increase in trace metal deposition in coastal sediments. Provided that these trace metals have remained relatively immobile after deposition, their sedimentary enrichments can serve as records of local-regional pollution histories. Factors controlling this proxy potential include trace metal geochemistry (carrier-, and host phase affinity), and depositional environmental factors (redox variability, particulate shuttling, organic matter loading, bathymetry). Yet, the relative importance and interactions between these controls are still poorly understood, hampering the reliable use of trace metal-based environmental proxies. By summarizing nine site-specific correlation matrices of 16 metal (loid) s (Pb, Cd, Cu, Zn, Sb, Sn, Ni, As, Tl, V, Mo, U, Re, Fe, Mn, Al), total organic C, and S contents in short sediment cores into a single meta-matrix, we test a novel approach for quickly detecting common and contrasting trace metal enrichment patterns across different study locations. Our meta-matrix shows two trace metal groups, within which positive correlations of e.g., Pb, Cd, Zn, Cu, Sb suggest a primary "anthropogenically sourced" (group I) control, whereas known "redox-sensitive" (group II) trace metals (Mo, U, Re) are characterized by fewer positive correlations. However, some group I metals (Cd, Zn, Cu, Sb) also covary with group II metals, inferring that redox variability may obscure primary anthropogenic signals; Sb even shows advantages over Mo and U under oxic conditions. As a more robust pollution indicator we identified Pb; yet for reconstructing historical Pb atmospheric pollution signals (1970s Pb peak), it is crucial to consider the distance from shore. In near-shore environments, local (fluvial) pollution signals may overprint large-scale (atmospheric) signals. Our findings demonstrate that combining site-specific sedimentary correlation and distribution patterns with a meta-matrix considerably aids the understanding of trace metal sequestration in different coastal sedimentary environments, which thereby improves trace metal proxy reliability.
自19世纪以来迅速蔓延的工业化导致沿海沉积物中痕量金属沉积急剧增加。假设这些痕量金属在沉积后保持相对稳定,其在沉积物中的富集情况可作为当地 - 区域污染历史的记录。控制这种代理潜力的因素包括痕量金属地球化学(载体和宿主相亲和力)以及沉积环境因素(氧化还原变异性、颗粒穿梭、有机物质负荷、水深)。然而,这些控制因素之间的相对重要性和相互作用仍知之甚少,这妨碍了基于痕量金属的环境代理的可靠使用。通过将16种金属(类金属)(铅、镉、铜、锌、锑、锡、镍、砷、铊、钒、钼、铀、铼、铁、锰、铝)、总有机碳和硫含量在短沉积岩芯中的九个特定地点相关矩阵汇总为一个单一的元矩阵,我们测试了一种新方法,用于快速检测不同研究地点常见和对比的痕量金属富集模式。我们的元矩阵显示出两个痕量金属组,其中例如铅、镉、锌、铜、锑的正相关表明主要受“人为来源”(第一组)控制,而已知的“氧化还原敏感”(第二组)痕量金属(钼、铀、铼)的正相关较少。然而,一些第一组金属(镉、锌、铜、锑)也与第二组金属共变,这表明氧化还原变异性可能掩盖主要的人为信号;在有氧条件下,锑甚至比钼和铀表现出优势。作为一种更可靠的污染指标,我们确定了铅;然而,对于重建历史铅大气污染信号(20世纪70年代铅峰值),考虑到离海岸的距离至关重要。在近岸环境中,局部(河流)污染信号可能会覆盖大规模(大气)信号。我们的研究结果表明,将特定地点的沉积相关和分布模式与元矩阵相结合,极大地有助于理解不同沿海沉积环境中痕量金属的固存情况,从而提高痕量金属代理的可靠性。