Liu Juan, Wang Lulu, Lin Jingfen, Yuan Wenhuan, Li Liangzhong, Peng Yung-Kang, Xiong Xinni, Cao Huimin, Wei Xudong, Ouyang Qi'en, Lippold Holger, Wang Jin, Lin Ke
Key Laboratory of Water Quality and Conservation in the Pearl River Delta, Ministry of Education, School of Environmental Science and Engineering, Guangzhou University, Guangzhou, China.
CAS Key Laboratory of Renewable Energy, Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China.
Sci Total Environ. 2024 Feb 25;913:169542. doi: 10.1016/j.scitotenv.2023.169542. Epub 2023 Dec 21.
Thallium is a rare metal known for its highly toxic nature. Recent research has indicated that the precise determination of Tl isotopic compositions using Multi-Collector Inductively Coupled Plasma Mass Spectrometry (MC-ICP MS) provides new opportunities for understanding Tl geochemical behavior. While isotopic fractionation of Tl derived from anthropogenic activities (e.g., mining, smelting) have been reported, there is limited information regarding Tl influenced by both natural weathering processes and anthropogenic origins. Herein, we investigated, for the first time, the Tl isotopic compositions in soils across a representative Tl-rich depth profile from the Lanmuchang (LMC) quicksilver mine (southwest China) in the low-temperature metallogenesis zone. The results showed significant variations in Tl isotope signatures (εTl) among different soil layers, ranging from -0.23 to 3.79, with heavier isotope-Tl enrichment observed in the bottom layers of the profile (εTl = 2.18-3.79). This enrichment of Tl was not solely correlated with the degree of soil weathering but was also partially associated with oxidation of Tl(I) by Fe (hydr)oxide minerals. Quantitative calculation using εTl vs. 1/Tl data further indicated that the Tl enrichment across the soil depth profile was predominantly derived from anthropogenic origins. All these findings highlight that the robustness and reliability of Tl isotopes as a proxy for identifying both anthropogenic and geogenic sources, as well as tracing chemical alterations and redox-controlled mineralogical processes of Tl in soils. The nascent application of Tl isotopes herein not only offers valuable insights into the behavior of Tl in surface environments, but also establishes a framework for source apportionment in soils under similar circumstances.
铊是一种以高毒性著称的稀有金属。最近的研究表明,使用多接收电感耦合等离子体质谱仪(MC-ICP MS)精确测定铊的同位素组成,为理解铊的地球化学行为提供了新的机会。虽然已经报道了源自人为活动(如采矿、冶炼)的铊的同位素分馏情况,但关于受自然风化过程和人为来源共同影响的铊的信息有限。在此,我们首次研究了中国西南部低温成矿带兰木厂(LMC)汞矿一个具有代表性的富铊深度剖面土壤中的铊同位素组成。结果表明,不同土壤层之间铊同位素特征(εTl)存在显著差异,范围为-0.23至3.79,在剖面底层观察到较重同位素铊的富集(εTl = 2.18 - 3.79)。这种铊的富集不仅与土壤风化程度不完全相关,还部分与铁(氢)氧化物矿物对Tl(I)的氧化有关。使用εTl与1/Tl数据进行的定量计算进一步表明,整个土壤深度剖面的铊富集主要源自人为来源。所有这些发现突出了铊同位素作为识别自然和人为来源以及追踪土壤中铊的化学变化和氧化还原控制的矿物学过程的代理指标的稳健性和可靠性。本文中铊同位素的初步应用不仅为铊在地表环境中的行为提供了有价值的见解,还为类似情况下土壤中的源分配建立了框架。