The Steptoean Positive Carbon Isotope Excursion (SPICE), inorganic aragonite precipitation and sea water chemistry: Insights from the Middle–Late Cambrian Port au Port Group, Newfoundland

IF 1.9 3区 地球科学 Q1 GEOLOGY Depositional Record Pub Date : 2021-10-29 DOI:10.1002/dep2.172
Joyce E. Neilson, Rosalia Barili, Alexander Brasier, Luiz F. De Ros, Sarah Ledingham
{"title":"The Steptoean Positive Carbon Isotope Excursion (SPICE), inorganic aragonite precipitation and sea water chemistry: Insights from the Middle–Late Cambrian Port au Port Group, Newfoundland","authors":"Joyce E. Neilson,&nbsp;Rosalia Barili,&nbsp;Alexander Brasier,&nbsp;Luiz F. De Ros,&nbsp;Sarah Ledingham","doi":"10.1002/dep2.172","DOIUrl":null,"url":null,"abstract":"<p>The Late Cambrian Steptoean Positive Carbon Isotope Excursion marks a time of significant change in ocean chemistry and trilobite faunas. On the lead up to the carbon isotope excursion and at the excursion itself, there is global evidence from Laurentia and Gondwana of cementation by primary aragonite in shallow subtidal environments accompanied by deposition of aragonitic ooids. However, this occurred at a time widely considered to have been characterised by ‘calcite seas’ when the primary inorganic phases (marine cements and ooids) are normally presumed calcitic. This study has investigated the chemostratigraphy of the Middle–Late Cambrian Port au Port Group, Newfoundland, including the early marine cements. Here, the marine cements contain increasing concentrations of strontium towards the peak carbon isotope excursion (up to 5500 ppm at the peak excursion) before dropping off post-peak excursion, consistent with the original cements having been aragonitic. This trend is accompanied by relict oomouldic porosity, again suggesting an aragonitic precursor. Primary inorganic mineralogy is largely controlled by the Mg/Ca ratio of sea water but estimates of the Mg/Ca ratio of Late Cambrian oceans are variable (0.8–2). At this level, other factors such as water temperature and pCO<sub>2</sub> have been shown to affect mineralogy with warm waters and high levels of CO<sub>2</sub> favouring aragonite. It is possible that the warm waters and anoxia that caused the carbon isotope excursion created conditions favourable for the precipitation of aragonite at the same time as major trilobite faunal turnover.</p>","PeriodicalId":54144,"journal":{"name":"Depositional Record","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2021-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/dep2.172","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Depositional Record","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/dep2.172","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: 3

Abstract

The Late Cambrian Steptoean Positive Carbon Isotope Excursion marks a time of significant change in ocean chemistry and trilobite faunas. On the lead up to the carbon isotope excursion and at the excursion itself, there is global evidence from Laurentia and Gondwana of cementation by primary aragonite in shallow subtidal environments accompanied by deposition of aragonitic ooids. However, this occurred at a time widely considered to have been characterised by ‘calcite seas’ when the primary inorganic phases (marine cements and ooids) are normally presumed calcitic. This study has investigated the chemostratigraphy of the Middle–Late Cambrian Port au Port Group, Newfoundland, including the early marine cements. Here, the marine cements contain increasing concentrations of strontium towards the peak carbon isotope excursion (up to 5500 ppm at the peak excursion) before dropping off post-peak excursion, consistent with the original cements having been aragonitic. This trend is accompanied by relict oomouldic porosity, again suggesting an aragonitic precursor. Primary inorganic mineralogy is largely controlled by the Mg/Ca ratio of sea water but estimates of the Mg/Ca ratio of Late Cambrian oceans are variable (0.8–2). At this level, other factors such as water temperature and pCO2 have been shown to affect mineralogy with warm waters and high levels of CO2 favouring aragonite. It is possible that the warm waters and anoxia that caused the carbon isotope excursion created conditions favourable for the precipitation of aragonite at the same time as major trilobite faunal turnover.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
阶阶正碳同位素偏移(SPICE)、无机文石沉淀和海水化学:来自纽芬兰中晚寒武世Port au Port群的启示
晚寒武世阶梯阶正碳同位素偏移标志着海洋化学和三叶虫动物群发生重大变化的时期。在碳同位素漂移之前和漂移本身,Laurentia和Gondwana的全球证据表明,在浅海潮下环境中,原生文石胶结伴随着文石卵体的沉积。然而,这发生在一个被广泛认为具有“方解石海”特征的时期,当时的初级无机相(海洋胶结物和流体)通常被认为是方解石相。研究了纽芬兰中晚寒武统Port au Port群的化学地层学,包括早期海相胶结物。在这里,海洋胶结物中锶的浓度在碳同位素峰值偏移时增加(峰值偏移时达到5500 ppm),然后在峰后偏移时下降,这与原始胶结物为文石相一致。这种趋势伴随着残余的模塑孔隙,再次表明文石前体。原生无机矿物学在很大程度上受海水Mg/Ca比值的控制,但对晚寒武世海洋Mg/Ca比值的估计是可变的(0.8-2)。在这个水平上,水温和二氧化碳分压等其他因素已被证明会影响矿物学,温暖的海水和高水平的二氧化碳有利于文石。在三叶虫主要区系更替的同时,引起碳同位素偏移的暖水和缺氧可能为文石的降水创造了有利条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 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
期刊最新文献
Issue Information Changes in mesophotic carbonate-platform export across the end of the last glacial cycle (Saya de Malha Bank, western Indian Ocean) Evolution of a late Quaternary succession by interpretation of high-resolution seismic and bathymetric data, Adriatic Sea Chronostratigraphy and tectono-sedimentary history of the Eastern South Pyrenean foreland basin (Ripoll Syncline, North-East Spain) Issue Information
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1