{"title":"CaCO3在自然和人工水生环境中的降水。机制、类似物和代用物","authors":"Martin Dietzel, Ronny Boch","doi":"10.1016/j.chemer.2024.126206","DOIUrl":null,"url":null,"abstract":"<div><div>Calcium carbonate precipitates occur in diverse and widespread aquatic environments, both from marine to terrestrial natural surroundings and from anthropogenic to engineered settings. In aquatic media, calcium and carbonate ions react to form hydrous and anhydrous CaCO<sub>3</sub>-containig solids in types of amorphous and crystalline phases, with calcite, aragonite and dolomite being the most frequent carbonate minerals in the Earth's crust. Understanding the CaCO<sub>3</sub> formation kinetics and mechanisms is key to exploring and evaluating individual aspects of biomineralization, speleothem and travertine growth, lime−/dolostone genesis, diagenetic pathways, climate reconstruction, CO<sub>2</sub> sequestration, tailored synthesis, unwanted scaling, mediated cementation, (geo)chemical forensics, etc. Although the literature dealing with CaCO<sub>3</sub> abundance, formation conditions, reaction mechanisms, nano- and macrostructures, elemental and isotope proxies is extensive, a comprehensive and up-to-date review of the highly diverse environments of CaCO<sub>3</sub> precipitation from aqueous media is valuable due to the tremendous increase in our knowledge about (i) CaCO<sub>3</sub> formation settings, analogues, reaction dynamics, and (potential) applications, (ii) novel high-precision, temporally and spatially highly-resolved analytical techniques, and (iii) monitoring, tracing and modeling tools. The present review on the formation of CaCO<sub>3</sub> in natural and man-made aquatic environments focuses on a systematic compilation and assessment of (i) reaction kinetics, mechanisms, and pathways of carbonate precipitation, (ii) analytical tools and proxies for tracking and reconstructing the solid-fluid-gas interactions and physico(<em>bio</em>)chemical environmental conditions during CaCO<sub>3</sub> precipitation, and (iii) natural and man-made analogs for the precipitation settings. The present review approach is not encyclopedic, but aims at a diverse array of environmental settings, the complex and coupled reaction pathways, state-of-the-art elemental and isotopic environmental proxies, and novel monitoring and modeling concepts for CaCO<sub>3</sub> precipitation.</div></div>","PeriodicalId":55973,"journal":{"name":"Chemie Der Erde-Geochemistry","volume":"84 4","pages":"Article 126206"},"PeriodicalIF":2.6000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Precipitation of CaCO3 in natural and man-made aquatic environments - Mechanisms, analogues, and proxies\",\"authors\":\"Martin Dietzel, Ronny Boch\",\"doi\":\"10.1016/j.chemer.2024.126206\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Calcium carbonate precipitates occur in diverse and widespread aquatic environments, both from marine to terrestrial natural surroundings and from anthropogenic to engineered settings. In aquatic media, calcium and carbonate ions react to form hydrous and anhydrous CaCO<sub>3</sub>-containig solids in types of amorphous and crystalline phases, with calcite, aragonite and dolomite being the most frequent carbonate minerals in the Earth's crust. Understanding the CaCO<sub>3</sub> formation kinetics and mechanisms is key to exploring and evaluating individual aspects of biomineralization, speleothem and travertine growth, lime−/dolostone genesis, diagenetic pathways, climate reconstruction, CO<sub>2</sub> sequestration, tailored synthesis, unwanted scaling, mediated cementation, (geo)chemical forensics, etc. Although the literature dealing with CaCO<sub>3</sub> abundance, formation conditions, reaction mechanisms, nano- and macrostructures, elemental and isotope proxies is extensive, a comprehensive and up-to-date review of the highly diverse environments of CaCO<sub>3</sub> precipitation from aqueous media is valuable due to the tremendous increase in our knowledge about (i) CaCO<sub>3</sub> formation settings, analogues, reaction dynamics, and (potential) applications, (ii) novel high-precision, temporally and spatially highly-resolved analytical techniques, and (iii) monitoring, tracing and modeling tools. The present review on the formation of CaCO<sub>3</sub> in natural and man-made aquatic environments focuses on a systematic compilation and assessment of (i) reaction kinetics, mechanisms, and pathways of carbonate precipitation, (ii) analytical tools and proxies for tracking and reconstructing the solid-fluid-gas interactions and physico(<em>bio</em>)chemical environmental conditions during CaCO<sub>3</sub> precipitation, and (iii) natural and man-made analogs for the precipitation settings. The present review approach is not encyclopedic, but aims at a diverse array of environmental settings, the complex and coupled reaction pathways, state-of-the-art elemental and isotopic environmental proxies, and novel monitoring and modeling concepts for CaCO<sub>3</sub> precipitation.</div></div>\",\"PeriodicalId\":55973,\"journal\":{\"name\":\"Chemie Der Erde-Geochemistry\",\"volume\":\"84 4\",\"pages\":\"Article 126206\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemie Der Erde-Geochemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0009281924001314\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GEOCHEMISTRY & GEOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemie Der Erde-Geochemistry","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0009281924001314","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
Precipitation of CaCO3 in natural and man-made aquatic environments - Mechanisms, analogues, and proxies
Calcium carbonate precipitates occur in diverse and widespread aquatic environments, both from marine to terrestrial natural surroundings and from anthropogenic to engineered settings. In aquatic media, calcium and carbonate ions react to form hydrous and anhydrous CaCO3-containig solids in types of amorphous and crystalline phases, with calcite, aragonite and dolomite being the most frequent carbonate minerals in the Earth's crust. Understanding the CaCO3 formation kinetics and mechanisms is key to exploring and evaluating individual aspects of biomineralization, speleothem and travertine growth, lime−/dolostone genesis, diagenetic pathways, climate reconstruction, CO2 sequestration, tailored synthesis, unwanted scaling, mediated cementation, (geo)chemical forensics, etc. Although the literature dealing with CaCO3 abundance, formation conditions, reaction mechanisms, nano- and macrostructures, elemental and isotope proxies is extensive, a comprehensive and up-to-date review of the highly diverse environments of CaCO3 precipitation from aqueous media is valuable due to the tremendous increase in our knowledge about (i) CaCO3 formation settings, analogues, reaction dynamics, and (potential) applications, (ii) novel high-precision, temporally and spatially highly-resolved analytical techniques, and (iii) monitoring, tracing and modeling tools. The present review on the formation of CaCO3 in natural and man-made aquatic environments focuses on a systematic compilation and assessment of (i) reaction kinetics, mechanisms, and pathways of carbonate precipitation, (ii) analytical tools and proxies for tracking and reconstructing the solid-fluid-gas interactions and physico(bio)chemical environmental conditions during CaCO3 precipitation, and (iii) natural and man-made analogs for the precipitation settings. The present review approach is not encyclopedic, but aims at a diverse array of environmental settings, the complex and coupled reaction pathways, state-of-the-art elemental and isotopic environmental proxies, and novel monitoring and modeling concepts for CaCO3 precipitation.
期刊介绍:
GEOCHEMISTRY was founded as Chemie der Erde 1914 in Jena, and, hence, is one of the oldest journals for geochemistry-related topics.
GEOCHEMISTRY (formerly Chemie der Erde / Geochemistry) publishes original research papers, short communications, reviews of selected topics, and high-class invited review articles addressed at broad geosciences audience. Publications dealing with interdisciplinary questions are particularly welcome. Young scientists are especially encouraged to submit their work. Contributions will be published exclusively in English. The journal, through very personalized consultation and its worldwide distribution, offers entry into the world of international scientific communication, and promotes interdisciplinary discussion on chemical problems in a broad spectrum of geosciences.
The following topics are covered by the expertise of the members of the editorial board (see below):
-cosmochemistry, meteoritics-
igneous, metamorphic, and sedimentary petrology-
volcanology-
low & high temperature geochemistry-
experimental - theoretical - field related studies-
mineralogy - crystallography-
environmental geosciences-
archaeometry