夏威夷和埃内韦塔克近海的深海成岩作用,对较老的碳酸盐岩有影响

IF 1.9 3区 地球科学 Q1 GEOLOGY
Arthur Saller, Charlotte Winterbottom
{"title":"夏威夷和埃内韦塔克近海的深海成岩作用,对较老的碳酸盐岩有影响","authors":"Arthur Saller,&nbsp;Charlotte Winterbottom","doi":"10.1002/dep2.216","DOIUrl":null,"url":null,"abstract":"<p>Cenozoic limestones from Hawaii and Enewetak were studied to characterise diagenesis in deep sea water. Hawaii samples were from subsea outcrops of drowned Pleistocene reefs 150–1,505 m deep (maximum age 550–600 ka). Most samples had early fibrous aragonite and high-magnesium calcite cements precipitated in shallow sea water. Partial dissolution of aragonite (including coral) and high-magnesium calcite were significant at 412 m and increased to 1,505 m. Crusts of ‘stubby’ sparry calcite cement (2–8 mol.% MgCO<sub>3</sub>; ‘lower Mg calcite’) precipitated on early aragonite and high-magnesium calcite cements at 473–1,358 m. Dissolution of aragonite and high-magnesium calcite was incomplete. Aragonite and high-magnesium calcite were not neomorphosed to low-magnesium calcite ( &lt;5 mol.% MgCO<sub>3</sub>). Enewetak well samples came from 3 to 1,400 m (Holocene to Upper Eocene). Lower Miocene to Upper Eocene carbonates at 380–1,380 m near the atoll margin showed pervasive dissolution of aragonite and conversion of high-magnesium calcite fossils to low-magnesium calcite. Their lower-Mg calcite cements (380–820 m; mainly radiaxial) were associated with aragonite dissolution. The lower-Mg calcite cements and bulk limestones below 500 m had geochemistry indicating precipitation or stabilisation in sea water at 10–27°C. Data indicate Enewetak dolomitisation (1,250–1,320 m) in cold sea water during burial &gt;1,000 m. Coralline algae showed little petrographic alteration, but Mg decreased downward from 15 to 1.5 mol.% MgCO<sub>3</sub>. In both areas, aragonite dissolution, alteration of high-magnesium calcite, and precipitation of lower-Mg calcite cements occurred in deep sea water (&gt;300 m) undersaturated for aragonite, but supersaturated for low-magnesium calcite. Original high-magnesium calcite was partially dissolved in Hawaii samples, but converted to low-magnesium calcite in deep Enewetak cores, possibly due to gradual deepening at Enewetak. Dolomitisation and low-magnesium calcite dissolution occurred below the calcite saturation depth (approximately 1,000 m) in Enewetak, but not deep Hawaii samples, possibly because dolomitisation is slower. Temporal variations in carbonate saturation, especially related to pCO<sub>2</sub>, are interpreted as the main control on mineralogy during marine diagenesis now and in many ancient oceans.</p>","PeriodicalId":54144,"journal":{"name":"Depositional Record","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2022-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/dep2.216","citationCount":"2","resultStr":"{\"title\":\"Deep marine diagenesis, offshore Hawaii and Enewetak, with implications for older carbonates\",\"authors\":\"Arthur Saller,&nbsp;Charlotte Winterbottom\",\"doi\":\"10.1002/dep2.216\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Cenozoic limestones from Hawaii and Enewetak were studied to characterise diagenesis in deep sea water. Hawaii samples were from subsea outcrops of drowned Pleistocene reefs 150–1,505 m deep (maximum age 550–600 ka). Most samples had early fibrous aragonite and high-magnesium calcite cements precipitated in shallow sea water. Partial dissolution of aragonite (including coral) and high-magnesium calcite were significant at 412 m and increased to 1,505 m. Crusts of ‘stubby’ sparry calcite cement (2–8 mol.% MgCO<sub>3</sub>; ‘lower Mg calcite’) precipitated on early aragonite and high-magnesium calcite cements at 473–1,358 m. Dissolution of aragonite and high-magnesium calcite was incomplete. Aragonite and high-magnesium calcite were not neomorphosed to low-magnesium calcite ( &lt;5 mol.% MgCO<sub>3</sub>). Enewetak well samples came from 3 to 1,400 m (Holocene to Upper Eocene). Lower Miocene to Upper Eocene carbonates at 380–1,380 m near the atoll margin showed pervasive dissolution of aragonite and conversion of high-magnesium calcite fossils to low-magnesium calcite. Their lower-Mg calcite cements (380–820 m; mainly radiaxial) were associated with aragonite dissolution. The lower-Mg calcite cements and bulk limestones below 500 m had geochemistry indicating precipitation or stabilisation in sea water at 10–27°C. Data indicate Enewetak dolomitisation (1,250–1,320 m) in cold sea water during burial &gt;1,000 m. Coralline algae showed little petrographic alteration, but Mg decreased downward from 15 to 1.5 mol.% MgCO<sub>3</sub>. In both areas, aragonite dissolution, alteration of high-magnesium calcite, and precipitation of lower-Mg calcite cements occurred in deep sea water (&gt;300 m) undersaturated for aragonite, but supersaturated for low-magnesium calcite. Original high-magnesium calcite was partially dissolved in Hawaii samples, but converted to low-magnesium calcite in deep Enewetak cores, possibly due to gradual deepening at Enewetak. Dolomitisation and low-magnesium calcite dissolution occurred below the calcite saturation depth (approximately 1,000 m) in Enewetak, but not deep Hawaii samples, possibly because dolomitisation is slower. Temporal variations in carbonate saturation, especially related to pCO<sub>2</sub>, are interpreted as the main control on mineralogy during marine diagenesis now and in many ancient oceans.</p>\",\"PeriodicalId\":54144,\"journal\":{\"name\":\"Depositional Record\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2022-12-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/dep2.216\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Depositional Record\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/dep2.216\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GEOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Depositional Record","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/dep2.216","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOLOGY","Score":null,"Total":0}
引用次数: 2

摘要

研究了夏威夷和埃内韦塔克的新生代石灰岩,以表征深海中的成岩作用。夏威夷的样本来自150–1505年淹没的更新世珊瑚礁的海底露头 m深(最大年龄550–600 ka)。大多数样品具有在浅水中沉淀的早期纤维状霰石和高镁方解石胶结物。文石(包括珊瑚)和高镁方解石的部分溶解在412处显著 m,增加到1505 m.在473–1358年,“短粗”亮晶方解石胶结物(2–8 mol.%MgCO3;“低镁方解石”)的地壳沉淀在早期文石和高镁方解石胶结物上 m.霰石和高镁方解石的溶解不完全。Aragonite和高镁方解石未新生为低镁方解石(1000 m.珊瑚藻几乎没有岩相变化,但Mg从15 mol.%MgCO3下降到1.5 mol.%MgCO3。在这两个区域,深海中都发生了霰石溶解、高镁方解石蚀变和低镁方解石胶结物沉淀(>300 m) 文石不饱和,但低镁方解石过饱和。原始的高镁方解石在夏威夷样品中部分溶解,但在Eneweak深部岩芯中转化为低镁方解石,这可能是由于Eneweaak的逐渐加深。白云石化和低镁方解石溶解发生在方解石饱和深度以下(约1000 m) Enewetak,但不是夏威夷的深层样品,可能是因为白云石化作用较慢。碳酸盐饱和度的时间变化,特别是与pCO2有关的变化,被解释为现在和许多古代海洋成岩过程中矿物学的主要控制因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deep marine diagenesis, offshore Hawaii and Enewetak, with implications for older carbonates

Deep marine diagenesis, offshore Hawaii and Enewetak, with implications for older carbonates

Cenozoic limestones from Hawaii and Enewetak were studied to characterise diagenesis in deep sea water. Hawaii samples were from subsea outcrops of drowned Pleistocene reefs 150–1,505 m deep (maximum age 550–600 ka). Most samples had early fibrous aragonite and high-magnesium calcite cements precipitated in shallow sea water. Partial dissolution of aragonite (including coral) and high-magnesium calcite were significant at 412 m and increased to 1,505 m. Crusts of ‘stubby’ sparry calcite cement (2–8 mol.% MgCO3; ‘lower Mg calcite’) precipitated on early aragonite and high-magnesium calcite cements at 473–1,358 m. Dissolution of aragonite and high-magnesium calcite was incomplete. Aragonite and high-magnesium calcite were not neomorphosed to low-magnesium calcite ( <5 mol.% MgCO3). Enewetak well samples came from 3 to 1,400 m (Holocene to Upper Eocene). Lower Miocene to Upper Eocene carbonates at 380–1,380 m near the atoll margin showed pervasive dissolution of aragonite and conversion of high-magnesium calcite fossils to low-magnesium calcite. Their lower-Mg calcite cements (380–820 m; mainly radiaxial) were associated with aragonite dissolution. The lower-Mg calcite cements and bulk limestones below 500 m had geochemistry indicating precipitation or stabilisation in sea water at 10–27°C. Data indicate Enewetak dolomitisation (1,250–1,320 m) in cold sea water during burial >1,000 m. Coralline algae showed little petrographic alteration, but Mg decreased downward from 15 to 1.5 mol.% MgCO3. In both areas, aragonite dissolution, alteration of high-magnesium calcite, and precipitation of lower-Mg calcite cements occurred in deep sea water (>300 m) undersaturated for aragonite, but supersaturated for low-magnesium calcite. Original high-magnesium calcite was partially dissolved in Hawaii samples, but converted to low-magnesium calcite in deep Enewetak cores, possibly due to gradual deepening at Enewetak. Dolomitisation and low-magnesium calcite dissolution occurred below the calcite saturation depth (approximately 1,000 m) in Enewetak, but not deep Hawaii samples, possibly because dolomitisation is slower. Temporal variations in carbonate saturation, especially related to pCO2, are interpreted as the main control on mineralogy during marine diagenesis now and in many ancient oceans.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.10
自引率
16.70%
发文量
42
审稿时长
16 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信