Zhang Hui, Fu Xuewu, Wu Xian, Deng Qianwen, Tang Kaihui, Zhang Leiming, Sommar Jonas Olof, Feng Xinbin
State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550081, PR China.
State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550081, PR China.
Water Res. 2025 Sep 1;283:123820. doi: 10.1016/j.watres.2025.123820. Epub 2025 May 13.
Identification of sources, transport pathways, and transformation mechanisms of mercury (Hg) is fundamental to our understanding of the biogeochemical cycling of Hg in lake ecosystems. In this study, we conducted a comprehensive investigation on the isotopic compositions of Hg in water columns, sediments, atmospheric deposition endmembers, watershed river, and runoff in Hongfeng Lake (HFL) ecosystem in southwestern China. We observed significant difference in δHg between dissolved Hg (DHg) and particulate Hg (PHg) in lake, river, and runoff samples, with lighter isotopes preferentially adsorbed onto particulate matter. ∆Hg was also significantly higher for DHg than PHg in lake and river waters, primarily due to the higher susceptibility of DHg to photochemical reduction processes. ∆Hg and ∆Hg of Hg in sediments were similar to those of PHg in water column, but significantly different from those of DHg, reflecting the dominant role of sedimentation of PHg from water column in the Hg accumulation in sediments. The isotopic compositions of Hg in lake water and sediments lay between those of atmospheric deposition and watershed runoff end-members. Using a Hg isotope mass balance model, we estimated that runoff input accounted for 62.4 % of total Hg input into the HFL ecosystem, followed by riverine input (14.5 %), particulate-bound Hg (PBM) dry deposition (11.0 %), Hg(II) wet deposition (5.5 %), Hg(0) dry deposition (4.2 %), and gaseous oxidized Hg (GOM) dry deposition (2.4 %). These results highlight the key role of watershed runoff as a source of Hg in lake ecosystems and improve our understanding of the biogeochemical cycling of Hg such ecosystems.
确定汞(Hg)的来源、迁移途径和转化机制,对于我们理解湖泊生态系统中汞的生物地球化学循环至关重要。在本研究中,我们对中国西南部红枫湖(HFL)生态系统的水柱、沉积物、大气沉降端元、流域河流和径流中的汞同位素组成进行了全面调查。我们观察到,湖泊、河流和径流样品中溶解态汞(DHg)和颗粒态汞(PHg)的δHg存在显著差异,较轻的同位素优先吸附在颗粒物上。湖泊和河流水体中DHg的∆Hg也显著高于PHg,这主要是由于DHg对光化学还原过程的敏感性更高。沉积物中汞的∆Hg和∆Hg与水柱中PHg的相似,但与DHg的显著不同,这反映了水柱中PHg的沉降在沉积物汞积累中的主导作用。湖水和沉积物中汞的同位素组成介于大气沉降和流域径流端元之间。使用汞同位素质量平衡模型,我们估计径流输入占HFL生态系统总汞输入的62.4%,其次是河流输入(14.5%)、颗粒态汞(PBM)干沉降(11.0%)、Hg(II)湿沉降(5.5%)、Hg(0)干沉降(4.2%)和气态氧化汞(GOM)干沉降(2.4%)。这些结果突出了流域径流作为湖泊生态系统汞源的关键作用,并增进了我们对这类生态系统中汞生物地球化学循环的理解。