Elizabeth J. Trower, Brianna M. Hibner, Tyler A. Lincoln, Jacqueline E. Dodd, Cedric J. Hagen, Marjorie D. Cantine, Maya L. Gomes
{"title":"重新审视现代碳酸盐平台沉积物中升高的 δ13C 值","authors":"Elizabeth J. Trower, Brianna M. Hibner, Tyler A. Lincoln, Jacqueline E. Dodd, Cedric J. Hagen, Marjorie D. Cantine, Maya L. Gomes","doi":"10.1029/2023GL107703","DOIUrl":null,"url":null,"abstract":"<p>The measured carbon isotopic compositions of carbonate sediments (δ<sup>13</sup>C<sub>carb</sub>) on modern platforms are commonly <sup>13</sup>C-enriched compared to predicted values for minerals forming in isotopic equilibrium with the dissolved inorganic carbon (DIC) of modern seawater. This offset undermines the assumption that δ<sup>13</sup>C<sub>carb</sub> values of analogous facies in the rock record are an accurate archive of information about Earth's global carbon cycle. We present a new data set of the diurnal variation in carbonate chemistry and seawater δ<sup>13</sup>C<sub>DIC</sub> values on a modern carbonate platform. These data demonstrate that δ<sup>13</sup>C<sub>carb</sub> values on modern platforms are broadly representative of seawater, but only after accounting for the recent decrease in the δ<sup>13</sup>C value of atmospheric CO<sub>2</sub> and shallow seawater DIC due to anthropogenic carbon release, a phenomenon commonly referred to as the <sup>13</sup>C Suess effect. These findings highlight an important, yet overlooked, aspect of some modern carbonate systems, which must inform their use as ancient analogs.</p>","PeriodicalId":12523,"journal":{"name":"Geophysical Research Letters","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1029/2023GL107703","citationCount":"0","resultStr":"{\"title\":\"Revisiting Elevated δ13C Values of Sediment on Modern Carbonate Platforms\",\"authors\":\"Elizabeth J. Trower, Brianna M. Hibner, Tyler A. Lincoln, Jacqueline E. Dodd, Cedric J. Hagen, Marjorie D. Cantine, Maya L. Gomes\",\"doi\":\"10.1029/2023GL107703\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The measured carbon isotopic compositions of carbonate sediments (δ<sup>13</sup>C<sub>carb</sub>) on modern platforms are commonly <sup>13</sup>C-enriched compared to predicted values for minerals forming in isotopic equilibrium with the dissolved inorganic carbon (DIC) of modern seawater. This offset undermines the assumption that δ<sup>13</sup>C<sub>carb</sub> values of analogous facies in the rock record are an accurate archive of information about Earth's global carbon cycle. We present a new data set of the diurnal variation in carbonate chemistry and seawater δ<sup>13</sup>C<sub>DIC</sub> values on a modern carbonate platform. These data demonstrate that δ<sup>13</sup>C<sub>carb</sub> values on modern platforms are broadly representative of seawater, but only after accounting for the recent decrease in the δ<sup>13</sup>C value of atmospheric CO<sub>2</sub> and shallow seawater DIC due to anthropogenic carbon release, a phenomenon commonly referred to as the <sup>13</sup>C Suess effect. These findings highlight an important, yet overlooked, aspect of some modern carbonate systems, which must inform their use as ancient analogs.</p>\",\"PeriodicalId\":12523,\"journal\":{\"name\":\"Geophysical Research Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1029/2023GL107703\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Geophysical Research Letters\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1029/2023GL107703\",\"RegionNum\":1,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GEOSCIENCES, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geophysical Research Letters","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1029/2023GL107703","RegionNum":1,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOSCIENCES, MULTIDISCIPLINARY","Score":null,"Total":0}
Revisiting Elevated δ13C Values of Sediment on Modern Carbonate Platforms
The measured carbon isotopic compositions of carbonate sediments (δ13Ccarb) on modern platforms are commonly 13C-enriched compared to predicted values for minerals forming in isotopic equilibrium with the dissolved inorganic carbon (DIC) of modern seawater. This offset undermines the assumption that δ13Ccarb values of analogous facies in the rock record are an accurate archive of information about Earth's global carbon cycle. We present a new data set of the diurnal variation in carbonate chemistry and seawater δ13CDIC values on a modern carbonate platform. These data demonstrate that δ13Ccarb values on modern platforms are broadly representative of seawater, but only after accounting for the recent decrease in the δ13C value of atmospheric CO2 and shallow seawater DIC due to anthropogenic carbon release, a phenomenon commonly referred to as the 13C Suess effect. These findings highlight an important, yet overlooked, aspect of some modern carbonate systems, which must inform their use as ancient analogs.
期刊介绍:
Geophysical Research Letters (GRL) publishes high-impact, innovative, and timely research on major scientific advances in all the major geoscience disciplines. Papers are communications-length articles and should have broad and immediate implications in their discipline or across the geosciences. GRLmaintains the fastest turn-around of all high-impact publications in the geosciences and works closely with authors to ensure broad visibility of top papers.