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1.
铁元素是岩浆-热液成矿系统中参与成矿的重要金属元素之一,岩浆-热液矿床中富铁矿物(黄铁矿、磁铁矿、黄铜矿、磁黄铁矿、斑铜矿、毒砂、菱铁矿)的δ56Fe值变化较大(-2.07‰～+1.58‰),指示铁同位素在岩浆演化、流体出溶和热液演化过程中均存在明显的分馏,因此,在约束岩浆-热液成矿系统中成矿金属的迁移-富集-沉淀过程和示踪成矿物质来源方面具有巨大的应用潜力。通过整理和分析前人研究资料,文章总结了岩浆-热液成矿系统岩浆演化、流体出溶和热液演化过程中铁同位素地球化学行为的研究现状。岩浆演化过程中铁同位素会发生显著分馏,如部分熔融过程中,熔体相比残余固相富集重铁同位素;矿物分离结晶会引起残余熔体铁同位素组成的变化,主要受含Fe2+或Fe3+矿物结晶的影响,如磁铁矿分离结晶会导致残余熔体铁同位素组成变轻,总体反映岩浆氧化还原状态对铁同位素分馏的主要控制作用,因此,含矿岩体铁同位素组成及其变化可用于确定岩浆的氧化还原状态。流体出溶是含矿岩浆演化成为岩浆热液矿床的关键过程,出溶流体相对于母岩富集轻铁同位素,但实验研究表明出溶流体铁... 相似文献
2.
金厂河矿床是西南三江成矿省保山地块最具代表性的远端矽卡岩型多金属矿床之一,查明其成矿金属来源对理解该类矿床成因以及区域成矿规律具有重要意义。本文通过分析不同成矿阶段代表性含铁矿物的铁同位素组成,探讨其在成矿过程中的分馏机制,从而示踪成矿金属的源区特征。金厂河矽卡岩型矿床中成矿前阶段未蚀变的石榴子石和氧化物成矿阶段的磁铁矿均相对富集铁的重同位素,其δ;Fe值分别为0.05‰~0.16‰和0.07‰~0.18‰,而硫化物成矿阶段的黄铁矿和黄铜矿则相对富集铁的轻同位素,其δ;Fe值分别为-0.12‰~0.17‰和-0.54‰~-0.38‰,整体显示出从高氧逸度的成矿前阶段向低氧逸度的硫化物成矿阶段演化过程中矿物δ;Fe值逐渐降低的趋势,指示Fe;富集铁的重同位素,Fe;富集铁的轻同位素。同时,金厂河矿床各阶段矿物的δ;Fe值均显著低于碳酸盐围岩,而接近全球花岗岩的δ;Fe值,表明成矿的铁不是由围岩贡献,而是来自于隐伏的中酸性岩体。 相似文献
3.
锌同位素在矿床学中的应用：认识与进展 总被引：8，自引：1，他引：7
文章报道了安徽铜陵新桥和凤凰山矽卡岩型矿床中闪锌矿和共生黄铁矿间的Zn同位素组成,获得了锌同位素在这2个矿物间的分馏系数,系统总结了锌同位素在不同储库和不同类型矿床中的分布特征,结合最新的研究成果,较全面地总结了锌同位素在矿床学领域的应用,得出了锌同位素可以用来示踪流体演化和源区变化的基本认识。在成矿流体体系的演化过程中,随着矿物的沉淀,流体的逐渐富集重同位素,晚期矿物相对于早期矿物富集锌的重同位素。在热液流体对同一源区淋滤萃取的过程中,重同位素优先被淋滤出来,晚期淋滤出的流体相对早期淋滤出的流体富集轻同位素。 相似文献
4.
同位素示踪技术是矿床学研究的重要手段。近代成矿理论的许多重大进展都得益于同位素示踪技术(C、O、S、Pb、Sr、Nd等)的应用。新近发展起来的Fe同位素体系为直接示踪成矿物质来源和成矿作用过程提供了可能,但如何运用这些新同位素技术对矿床学中的重大科学问题进行制约仍有待于探索。流体出溶和流体演化是 相似文献
5.
铜同位素在矿床学中的应用:认识与进展 总被引：7，自引：0，他引：7
在甘肃西峰剖面黄土样品的铜同位素组成测定基础上,讨论了地壳的平均铜同位素组成.根据铜同位素在不同储库、不同类型矿床和不同矿物中的分布特征,认为铜同位素可以用来指示成矿温度、源区变化、流体出溶过程、矿化过程和次生富集过程等与成矿作用相关的信息.具体表现在:低温环境下形成的矿物比高温环境下形成的矿物具有更大的铜同位素组成变化范围;流体出溶过程中,铜同位素会发生分馏,早期出溶的流体富集铜的轻同位素,晚期出溶的流体富集铜的重同位素;同一矿化集中区内,根据同类型矿床间的铜同位素分布特征可以判别出其是否为同一矿化事件的产物;热液萃取源区铜的过程中,铜的重同位素优先从源区中淋滤出来.此外,在成矿体系中,淋滤帽富集轻同位素的特征可能暗示其下部存在铜矿化富集带. 相似文献
6.
确定金属矿床成矿物质的来源才能更好的探讨金属矿床的矿床成因、总结其成矿规律、为地质找矿服务。目前在成矿物质来源研究中常需要依据其他科学方法来间接测定和推断矿质的大致来源,硫同位素示踪研究就是其方法之一。应用硫同位素可以有效示踪金属矿床中成矿物质的来源、成矿流体搬运及成矿机制、矿床成因等。但硫同位素在示踪金属矿床中成矿物质来源时,因不同金属矿床的地质特征、成矿流体演化的物理化学条件以及矿物组合规律差异都会对判断硫源有影响,因此不但要选择合适方法成功获取成矿流体的δ34S∑S数据,还需具体的分析金属矿床的地质特征,采用多元的示踪方法相结合,让示踪结果更准确地接近地质事实,这样才能更好的确定金属矿床中成矿物质的来源。 相似文献
7.
根据矿床地质背景、热液蚀变组合、流体包裹体和稳定同位素地球化学，特别是根据浅成岩浆热液环境中特征矿物明矾石的稳定同位素组成，研究岩浆成矿流体的来源、动态与化成矿机理，获得了许多新认识；根据δ＾１４Ｓ和δ＾１８Ｏ可将明矾石划分出两种不同的成因类型；岩浆成矿热液在时间上从早期的气相流体向主成矿期的液相流体演化，而岩浆热液矿床在空间上主要定位于脆性－延性过渡带。 相似文献
8.
大兴安岭南段敖仑花斑岩钼(铜)矿床成矿流体来源与成矿作用:稳定同位素C、H、O、S和放射性Pb同位素约束 总被引：2，自引：0，他引：2
基于稳定同位素C、H、O、S和放射性Pb同位素的测试和分析,对大兴安岭南段敖仑花斑岩钼(铜)矿床成矿流体的来源进行了示踪,探讨了流体演化与成矿作用过程。新的稳定同位素数据显示:敖仑花矿床成矿热液具有混合来源性质;脉石矿物石英中流体的C、H、O同位素和矿石硫化物的S同位素组成指示成矿络合剂主要来自地幔,同时在热液期经历了地壳流体参与的过程;辉钼矿中放射性成因的Pb同位素组成表明,成矿物质(Mo)主要来自造山带物质,部分来自深部幔源。根据H、O同位素组成变化和已有流体包裹体资料,认为敖仑花矿床早、中阶段两次矿化的成矿机制不同:早阶段金属矿化主要与岩浆水和大气降水的流体混合有关,而中阶段大规模成矿作用主要是由流体沸腾所致。综合区域地质演化认为:敖仑花矿床是大兴安岭南段在晚侏罗世—早白垩世时期演化为弧后伸展背景、陆内造山带物质重新活化、壳幔岩浆-热液相互作用的产物,同时暗示壳幔作用强烈的地区利于内生金属矿床成矿。 相似文献
9.
阿西金矿床流体成矿的地球化学示踪研究 总被引：8，自引：0，他引：8
依据阿西金矿床Ｈ、Ｏ同位素组成特点对成矿流体的来源进行了示踪研究,并且研究了矿床的水岩交换作用,讨论了水－岩作用与金成矿的关系。根据矿床中典型热液矿物和岩矿石的稀土元素地球化学特征对成矿流体作用过程进行了示踪研究,与同位素地球化学示踪研究取得了基本一致的结果。根据成矿流体活动踪迹建立找矿标志,是进行矿产资源预测的新思路。 相似文献
10.
热液型矿床形成过程中流体的组成、运移、演化及其矿质沉淀机制是矿床学研究的重点内容和难点。矽卡岩矿床中具有震荡环带结构的石榴子石完整记录了热液流体的性质、组成及演化过程,这种震荡环带的出现暗示了不同成分系列的石榴子石对不同阶段热液流体成矿物化环境的特定选择性。石榴子石晶体元素化学分带现象是流体运移和矿物再沉淀过程周期性循环再现的结果,对指示早期矽卡岩阶段热液流体中主、微量元素化学分带机制具有重要意义。不同成分系列、不同期次石榴子石的Fe_2O_3和Al_2O_3含量差异显著,其对热液流体演化过程中氧化还原环境的变化具有较好的示踪作用;相对主量元素而言,微量元素在流体演化过程中具有更好的探针作用,钙铝榴石常富集Al、Ti、Zr、HREE元素,而钙铁榴石常富集As、W、Mo、Fe、LREE元素。借助EMPA和LA_ICP_MS技术对具震荡环带结构的石榴子石进行主、微量元素(包括稀土元素)的微区和原位分析是探讨成矿过程中流体组成和性质演化的重要手段,其有可能揭示矿物生长机制、成矿环境以及成矿流体组成与性质的演化,而这一地质信息对于全面理解矽卡岩型矿床的矿化分带及成矿作用非常重要。 相似文献
11.
Yue Wang Xiang-kun Zhu Jing-wen Mao Zhi-hong Li Yan-bo Cheng 《Ore Geology Reviews》2011,43(1):194-202
Fe isotope compositions of mineral separates and bulk samples from Xinqiao Cu–S–Fe–Au skarn type deposit were investigated. An overall variation in δ57Fe values from − 1.22‰ to + 0.73‰ has been observed, which shows some regularity. The δ57Fe values of endoskarn and the earliest formed Fe-mineral phase magnetite are ca.1.2‰ and ca. 0.3‰ lower, respectively, relative to the quartz–monzodiorite stock, indicating that fluid exsolved from the stock is enriched in light Fe isotopes. Moreover, spatial and temporal variations in δ57Fe values are observed, which suggest iron isotope fractionation during fluid evolution. Precipitation of Fe-bearing minerals results in the Fe isotope composition of residual fluids evolving with time. Precipitation of Fe (III) minerals incorporating heavy iron isotopes preferentially leaves the remaining fluid enriched in light isotopes, while precipitation of Fe (II) minerals preferentially taking-up light iron isotopes, and makes the Fe isotopic composition of the fluid progressively heavier. The regularity of Fe isotope variations occurred during fluid exsolution and evolution indicates that the dominant Fe source of Xinqiao deposit is magmatic. Overall, this study demonstrates that Fe isotope composition has great potential in unraveling ore-forming processes, as well as constraining the metal sources of ore deposits. 相似文献
12.
不同地质储库中的镁同位素组成及碳酸盐矿物形成过程中的镁同位素分馏控制因素 总被引：1，自引：1，他引：0
镁同位素在低温地球化学过程中显著的分馏效应,是其示踪地球表生环境演化及物质循环的基础。本文在前人研究的基础上,对地球上不同地质储库中的镁同位素组成及碳酸盐矿物形成过程中的镁同位素分馏控制因素进行了总结:火成岩的镁同位素组成较均一;风化产物总体富集重的镁同位素,且变化较大;碳酸盐岩中灰岩相对白云岩富集轻的镁同位素,但总体上富集轻的镁同位素;岩石类型、风化强度以及植被等因素对河流地表水的镁同位素组成影响较大,导致地表水的镁同位素组成总体变化较大;海水的镁同位素组成均一,平均值约为-0.83‰;低温条件下,控制碳酸盐矿物无机成因过程中镁同位素分馏的因素有矿物相、沉淀速率和温度,其中矿物相是主要控制因素;生物成因碳酸盐矿物镁同位素组成与生物体对含镁碳酸盐矿物的利用形式有关,除了需考虑与无机碳酸盐沉淀类似的控制因素外,还需考虑不同物种对轻、重镁同位素的选择性吸收能力;因生物成因海相碳酸盐矿物几乎都是由最初的无定形相碳酸盐转变而来,故生物成因海相碳酸盐矿物的镁同位素特征不能代表生成无定形相碳酸盐的流体的镁同位素特征。镁同位素在低温条件下具有良好的分馏效应,随着分析测试技术的发展及不同地质储库中镁同位素组成数据的积累和完善,有关表生环境中镁同位素分馏机制的许多问题将逐步得到解决,镁同位素在揭示地球表生环境演化及物质循环方面将发挥更大的作用。 相似文献
13.
Iron isotopes fractionate during hydrothermal processes. Therefore, the Fe isotope composition of ore-forming minerals characterizes either iron sources or fluid histories. The former potentially serves to distinguish between sedimentary, magmatic or metamorphic iron sources, and the latter allows the reconstruction of precipitation and redox processes. These processes take place during ore formation or alteration. The aim of this contribution is to investigate the suitability of this new isotope method as a probe of ore-related processes. For this purpose 51 samples of iron ores and iron mineral separates from the Schwarzwald region, southwest Germany, were analyzed for their iron isotope composition using multicollector ICP-MS. Further, the ore-forming and ore-altering processes were quantitatively modeled using reaction path calculations. The Schwarzwald mining district hosts mineralizations that formed discontinuously over almost 300 Ma of hydrothermal activity. Primary hematite, siderite and sulfides formed from mixing of meteoric fluids with deeper crustal brines. Later, these minerals were partly dissolved and oxidized, and secondary hematite, goethite and iron arsenates were precipitated. Two types of alteration products formed: (1) primary and high-temperature secondary Fe minerals formed between 120 and 300 °C, and (2) low-temperature secondary Fe minerals formed under supergene conditions (<100 °C). Measured iron isotope compositions are variable and cover a range in δ56Fe between −2.3‰ and +1.3‰. Primary hematite (δ56Fe: −0.5‰ to +0.5‰) precipitated by mixing oxidizing surface waters with a hydrothermal fluid that contained moderately light Fe (δ56Fe: −0.5‰) leached from the crystalline basement. Occasional input of CO2-rich waters resulted in precipitation of isotopically light siderite (δ56Fe: −1.4 to −0.7‰). The difference between hematite and siderite is compatible with published Fe isotope fractionation factors. The observed range in isotopic compositions can be accounted for by variable fractions of Fe precipitating from the fluid. Therefore, both fluid processes and mass balance can be inferred from Fe isotopes. Supergene weathering of siderite by oxidizing surface waters led to replacement of isotopically light primary siderite by similarly light secondary hematite and goethite, respectively. Because this replacement entails quantitative transfer of iron from precursor mineral to product, no significant isotope fractionation is produced. Hence, Fe isotopes potentially serve to identify precursors in ore alteration products. Goethites from oolitic sedimentary iron ores were also analyzed. Their compositional range appears to indicate oxidative precipitation from relatively uniform Fe dissolved in coastal water. This comprehensive iron isotope study illustrates the potential of the new technique in deciphering ore formation and alteration processes. Isotope ratios are strongly dependent on and highly characteristic of fluid and precipitation histories. Therefore, they are less suitable to provide information on Fe sources. However, it will be possible to unravel the physico-chemical processes leading to the formation, dissolution and redeposition of ores in great detail. 相似文献
14.
高温下非传统稳定同位素分馏 总被引：5，自引：1，他引：4
过去十几年来,非传统稳定同位素地球化学在高温地质过程的研究中取得了的重大进展。多接收诱导耦合等离子质谱(MC-ICP-MS)的应用引发了稳定同位素分析方法的重大突破,使得精确测定重元素的同位素比值成为可能。本文总结了以Li、Fe和Mg同位素为代表的非传统稳定同位素在岩石地球化学研究中的应用。Li同位素目前被广泛地用于地幔地球化学、俯冲带物质再循环和变质作用的研究中,可以用来示踪岩浆的源区性质和扩散等动力学过程。不同价态的Fe在矿物熔体相之间的分配可以产生Fe同位素分馏,可以发生在地幔交代、部分熔融、分离结晶等过程中。岩浆岩的Mg同位素则大致反映其源区的特征,地幔的Mg同位素组成比较均一,这为研究低温地球化学过程中Mg同位素的分馏提供一个均一的背景。此外,Cl,Si,Cu,Ca,U等等同位素体系也具有广阔的应用前景。对同位素分馏机制的实验研究和理论模拟为理解非传统稳定同位素数据提供了必要的指导。实验表明,高温下具有不同的迁移速度的轻、重同位素可以产生显著的动力学同位素分馏,这一分馏可以在化学扩散、蒸发和凝华等过程中发生;同位素在矿物和熔体以及流体相中化学环境的差异使得不同相之间可以发生平衡分馏。而最近的硅酸盐岩浆的热扩散和热迁移实验则揭示了一种"新"的岩浆分异和同位素分馏机制。沿着温度梯度,硅酸盐岩浆可以发生显著的元素和同位素分异,湿的安山岩可以通过这种方式演变成花岗质成分,因此这个过程可能对陆壳的产生和演化有重大影响。如果温度梯度在岩浆作用中能长期存在,热扩散就可以产生稳定同位素的分馏,这一机制有别于传统的平衡和动力学同位素分馏。 而多个稳定同位素体系的正相关关系是示踪热迁移过程的最有力证据。在热扩散过程中,流体承载的物质的浓度和它的索瑞系数有关。但是这个系数对体系的很多参数非常敏感,变化极大,因此对热扩散效应的研究产生极大的困难。对热扩散实验的镁、钙和铁同位素测量表明,同位素比值的变化与体系的化学组成以及总温度无关,只和温度变化的幅度有关,这意味着即使元素的索瑞系数变化多端,某一元素的同位素之间的索瑞系数的差别总为常数。这一发现有助于简化对热扩散和索瑞系数这一基础物理问题的研究 。 相似文献
15.
矿床的形成受制于多种复杂的地质作用,包括全球尺度的板块构造运动、岩浆活动、变质沉积改造等过程,并普遍伴随热液活动、流体迁移、水-岩相互作用、元素分异及同位素分馏等一系列局部区域地质和地球化学过程.在过去的矿床学研究中,地球化学方法主要围绕在主、微量元素和传统的稳定同位素等手段,解决了很多矿床成因问题.但仍存在不少的多解和难解问题,比如许多矿床在矿化类型、蚀变分带与金属矿物组合方面具有诸多相似之处,常规地球化学指标难以区分.随着测试精度的提高和自然储库组成的完善,Li同位素近些年来已成为新兴的稳定同位素体系.Li同位素在自然界过程中高达80‰的同位素分馏使其具有更好的辨识能力,同时兼有直接和间接指示作用,有潜力成为研究各种复杂成矿过程的良好示踪剂.本文总结了近年来有关矿床学中Li同位素的研究和应用进展,以俯冲带成矿为主,阐述了斑岩型-热液矿床、伟晶岩型矿床和沉积矿床等类型矿床的Li同位素地球化学特征,并探究新的Li同位素方法在矿床中的应用前景.基于Li同位素体系在各类矿床的应用实例,我们认为Li同位素体系将为矿床学研究提供更多的指示信息和依据. 相似文献
16.
贫碳酸盐的蚀变洋壳具有与新鲜洋中脊玄武岩一致的Mg同位素组成，说明低温和高温洋壳蚀变不会导致Mg同位素分馏.大别山港河和花凉亭的早期变质脉比榴辉岩具有偏高的δ56Fe-δ26Mg值，而且早期到晚期变质脉的δ56Fe-δ26Mg值逐渐降低.这些结果说明，在流体-岩石反应和流体演化过程中，Fe-Mg同位素发生了显著的分馏，且矿物溶解-再沉淀是同位素分馏的控制因素.相比洋中脊玄武岩，蚀变洋壳和变质脉具有相似或偏高的δ56Fe-δ26Mg值，说明蚀变洋壳脱水产生的流体富集重Fe-Mg同位素，不能解释弧岩浆岩的轻Fe/重Mg同位素组成.因此，弧岩浆岩异常的Fe-Mg同位素组成是熔体提取和富集54Fe-26Mg的蛇纹岩流体交代地幔楔两个过程共同作用的结果. 相似文献
17.
汞作为一种重要的成矿元素,广泛分布于不同地质体中,并参与成岩成矿作用。随着质谱技术的飞跃发展,汞同位素地球化学研究取得引人瞩目的进展。汞同位素被广泛地应用于示踪地球表生生物地球化学过程及汞污染等。近年来,汞同位素又被应用于揭示行星的演化过程、识别地质历史时期大火成岩省及示踪矿床成矿物质来源等方面。本文在前人研究的基础上,对不同地质储库汞同位素组成进行了系统总结。陨石、岩浆岩、变质岩、沉积岩、火山气体等地质储库汞同位素组成变化较大,部分样品还显示非质量分馏信息。本文着重阐述了低温热液矿床(现代热泉、汞矿床、铅锌矿床、锑矿床、金矿床)汞的赋存状态及同位素组成特征,构筑了汞同位素体系的基本格架。结合最新的研究成果,较全面地总结了矿床成矿过程中可能会发生的汞同位素分馏机制。热液矿床中汞同位素的质量分馏可能由流体挥发或者沸腾作用、冷凝作用、氧化还原反应、硫化物沉淀等引起。岩矿石中汞同位素的非质量分馏信息可能是地质历史时期汞光化学作用的产物,或者是继承某一特定的源岩信息所致。因此,未来汞同位素在示踪低温热液矿床的成矿物质来源、刻画成矿流体演化过程方面具有较大的应用潜力。 相似文献
18.
Mirjam Kiczka Jan G. Wiederhold Jakob Frommer Stephan M. Kraemer Ruben Kretzschmar 《Geochimica et cosmochimica acta》2011,75(19):5559-5573
The chemical weathering of primary Fe-bearing minerals, such as biotite and chlorite, is a key step of soil formation and an important nutrient source for the establishment of plant and microbial life. The understanding of the relevant processes and the associated Fe isotope fractionation is therefore of major importance for the further development of stable Fe isotopes as a tracer of the biogeochemical Fe cycle in terrestrial environments. We investigated the Fe mineral transformations and associated Fe isotope fractionation in a soil chronosequence of the Swiss Alps covering 150 years of soil formation on granite. For this purpose, we combined for the first time stable Fe isotope analyses with synchrotron-based Fe-EXAFS spectroscopy, which allowed us to interpret changes in Fe isotopic composition of bulk soils, size fractions, and chemically separated Fe pools over time in terms of weathering processes. Bulk soils and rocks exhibited constant isotopic compositions along the chronosequence, whereas soil Fe pools in grain size fractions spanned a range of 0.4‰ in δ56Fe. The clay fractions (<2 μm), in which newly formed Fe(III)-(hydr)oxides contributed up to 50% of the total Fe, were significantly enriched in light Fe isotopes, whereas the isotopic composition of silt and sand fractions, containing most of the soil Fe, remained in the range described by biotite/chlorite samples and bulk soils. Iron pools separated by a sequential extraction procedure covered a range of 0.8‰ in δ56Fe. For all soils the lightest isotopic composition was observed in a 1 M NH2OH-HCl-25% acetic acid extract, targeting poorly-crystalline Fe(III)-(hydr)oxides, compared with easily leachable Fe in primary phyllosilicates (0.5 M HCl extract) and Fe in residual silicates. The combination of the Fe isotope measurements with the speciation data obtained by Fe-EXAFS spectroscopy permitted to quantitatively relate the different isotope pools forming in the soils to the mineral weathering reactions which have taken place at the field site. A kinetic isotope effect during the Fe detachment from the phyllosilicates was identified as the dominant fractionation mechanism in young weathering environments, controlling not only the light isotope signature of secondary Fe(III)-(hydr)oxides but also significantly contributing to the isotope signature of plants. The present study further revealed that this kinetic fractionation effect can persist over considerable reaction advance during chemical weathering in field systems and is not only an initial transient phenomenon. 相似文献
19.
Iron isotope fractionation during proton- and ligand-promoted dissolution of primary phyllosilicates
Mirjam Kiczka Jan G. Wiederhold Jakob Frommer Bernard Bourdon 《Geochimica et cosmochimica acta》2010,74(11):3112-6415
We studied stable iron isotope fractionation during dissolution of a biotite and chlorite enriched mineral fraction from granite by HCl and 5 mM oxalic acid in a pH range of 4-5.9. Batch experiments covered a time period from 2 h to 100 days and were performed at initial potassium concentrations of 0, 0.5, and 5 mM to induce different levels of biotite exfoliation. All experiments were kept anoxic to investigate solely the dissolution step without the influence of oxidation and precipitation of secondary Fe oxyhydroxides. Oxalic acid increased the release of Fe by a factor of ∼15 compared with the HCl experiments. Addition of 0.5 mM K to initial solutions in proton-promoted dissolution decreased the release of Fe by 30-65% depending on the dissolution stage. In ligand-controlled dissolution, K reduced the Fe release only to a minor extent. All solutions of the early dissolution stages were enriched in light Fe isotopes by up to −1.4‰ in δ56Fe compared with the isotopic composition of biotite and chlorite mineral separates, which we explained by a kinetic isotope effect. In proton-promoted dissolution, early released fractions of K-enriched experiments were significantly lighter (−0.7‰ to −0.9‰) than in the initially K-free experiments. The evolution of Fe isotope ratios in solution was modeled by a linear combination of kinetic isotope effects during two independent dissolution processes attacking different crystallographic sites. In ligand-controlled dissolution, K did not influence the kinetic isotope effect and the Fe isotope composition in solution in the late dissolution stages remained slightly lighter than the bulk composition of the biotite/chlorite enriched mineral fraction. This study demonstrates that the initial Fe weathering flux should be enriched in light Fe isotopes and that Fe isotope data in combination with dissolution kinetics and stoichiometry provide new insights into dissolution mechanisms. 相似文献