Textural and compositional complexities resulting from coupled dissolution-reprecipitation reactions in geomaterials

被引:138
|
作者
Altree-Williams, Alexander [1 ]
Pring, Allan [2 ]
Ngothai, Yung [1 ]
Brugger, Joel [3 ]
机构
[1] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5000, Australia
[2] Flinders Univ S Australia, Sch Chem & Phys Sci, Bedford Pk, SA 5042, Australia
[3] Monash Univ, Sch Earth Atmosphere & Environm, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
Dissolution and precipitation; Fluid-driven mineral transformations; Interface chemistry; Ore petrography; Pseudomorphism; Reactive transport; Reaction mechanism; Textural evolution; MINERAL REPLACEMENT REACTIONS; CALCIUM-CARBONATE; AQUEOUS-SOLUTIONS; GRAIN-BOUNDARIES; ALKALI FELDSPARS; SOLID-SOLUTIONS; CRYSTAL-GROWTH; HIGH-PRESSURE; FLUID-FLOW; PSEUDOMORPHIC REPLACEMENT;
D O I
10.1016/j.earscirev.2015.08.013
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Texture encompasses 'the overall appearance a rock has because of the size, shape, and arrangement of its constituent mineral grains'. Textural observations are crucial for deciphering the origin and geological history of rocks and their constituting minerals. In metamorphic and hydrothermal settings, textural observations hence serve to reconstruct the P,T path and the compositions and origins of the parent fluids. Over the past 13 years, a number of studies have emphasized the role of 'coupled dissolution reprecipitation reactions' (CDR) in geological systems. In these fluid-driven reactions, the replacement of one phase by another occurs via coupling between the dissolution of the parent and the precipitation of the product. In this paper we review the diversity of textures that arise from the CDR mechanism. The great diversity of textures relates to the diversity of mechanisms responsible for the coupling between dissolution and precipitation. Key parameters defining textures include volume change, the rate-limiting process, and the local composition at the mineral-fluid interface. In many of the reviewed examples, reaction mechanisms, rather than intensive properties such as P-T history, control the textures in the products, and far-from-equilibrium or local equilibriums at the mineral-fluid interface play a key role in controlling the final textures and mineral assemblages. These processes can also lead to the scavenging of trace elements from hydrothermal fluids. Because by nature CDR reactions are interface-controlled, many of the products are metastable, which further drives the reactions. These subsequent reactions can add to the textural complexity, or on the contrary obscure the original reaction mechanism. This review emphasizes the need to improve our understanding of reaction mechanisms, especially in systems containing even minor amounts of fluids (ore systems; metasomatic and metamorphic systems). Such a process-driven understanding is vital to supporting the petrological interpretation of textures. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:628 / 651
页数:24
相关论文
共 48 条
  • [41] A new mode of mineral replacement reactions involving the synergy between fluid-induced solid-state diffusion and dissolution-reprecipitation: A case study of the replacement of bornite by copper sulfides
    Adegoke, Idowu A.
    Xia, Fang
    Deditius, Artur P.
    Pearce, Mark A.
    Roberts, Malcolm P.
    Brugger, Joel
    GEOCHIMICA ET COSMOCHIMICA ACTA, 2022, 330 : 165 - 190
  • [42] Dissolution-reprecipitation vs. solid-state diffusion in electrum: Examples from metamorphosed Au-bearing, volcanogenic massive sulfide (VMS) deposits
    Liu, Haiming
    Beaudoin, Georges
    AMERICAN MINERALOGIST, 2021, 106 (10) : 1654 - 1667
  • [43] Hydrothermal alteration of aragonitic biocarbonates: assessment of micro- and nanostructural dissolution-reprecipitation and constraints of diagenetic overprint from quantitative statistical grain-area analysis
    Casella, Laura A.
    He, Sixin
    Griesshaber, Erika
    Fernandez-Diaz, Lourdes
    Greiner, Martina
    Harper, Elizabeth M.
    Jackson, Daniel J.
    Ziegler, Andreas
    Mavromatis, Vasileios
    Dietzel, Martin
    Eisenhauer, Anton
    Veintemillas-Verdaguer, Sabino
    Brand, Uwe
    Schmahl, Wolfgang W.
    BIOGEOSCIENCES, 2018, 15 (24) : 7451 - 7484
  • [44] U-Pb, trace element and Lu-Hf properties of unique dissolution-reprecipitation zircon from UHP eclogite in SW Sulu terrane, eastern China
    Liu, Fulai
    Gerdes, Axel
    Liu, Pinghua
    GONDWANA RESEARCH, 2012, 22 (01) : 169 - 183
  • [45] Nano-scale evidence for coupled interfacial dissolution-reprecipitation (CDR) controlling corrosion of alumina-forming austenitic (AFA) steel in static lead-bismuth eutectic (LBE) at 600°C
    Zhang, Decang
    Zhang, Xiaoxin
    Zou, Qing
    Zhang, Jun
    Ren, Hao
    Zeng, Xian
    Yan, Qingzhi
    CORROSION SCIENCE, 2025, 243
  • [46] Pseudomorphic Rhythmically Banded and Oscillatory Tetrahedrite–Tennantite Aggregates in the Darasun Gold Deposit (Eastern Transbaikalia, Russia): A Result of Coupled Dissolution–Reprecipitation Reactions
    N. G. Lyubimtseva
    N. S. Bortnikov
    S. E. Borisovsky
    O. V. Vikent’eva
    V. Yu. Prokofiev
    Doklady Earth Sciences, 2018, 483 : 1431 - 1436
  • [47] Coupled textural and compositional characterization of basaltic scoria: Insights into the transition from Strombolian to fire fountain activity at Mount Etna, Italy
    Polacci, M
    Corsaro, RA
    Andronico, D
    GEOLOGY, 2006, 34 (03) : 201 - 204
  • [48] Fabrication of calcite blocks from gypsum blocks by compositional transformation based on dissolution-precipitation reactions in sodium carbonate solution
    Ishikawa, Kunio
    Kawachi, Giichiro
    Tsuru, Kanji
    Yoshimoto, Ayami
    MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2017, 72 : 389 - 393