Mitigating the atmospheric CO2 increase and ocean acidification by adding limestone powder to upwelling regions

The feasibility of enhancing the absorption of CO2 from the atmosphere by adding calcium carbonate (CaCO3) powder to the ocean and of partially reversing the acidification of the ocean and the decrease in calcite supersaturation resulting from the absorption of anthropogenic CO2 is investigated. CaC...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Geophysical Research: Oceans 2008-04, Vol.113 (C4), p.n/a
1. Verfasser: Harvey, L. D. D.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue C4
container_start_page
container_title Journal of Geophysical Research: Oceans
container_volume 113
creator Harvey, L. D. D.
description The feasibility of enhancing the absorption of CO2 from the atmosphere by adding calcium carbonate (CaCO3) powder to the ocean and of partially reversing the acidification of the ocean and the decrease in calcite supersaturation resulting from the absorption of anthropogenic CO2 is investigated. CaCO3 could be added to the surface layer in regions where the depth of the boundary between supersaturated and unsaturated water is relatively shallow (250–500 m) and where the upwelling velocity is large (30–300 m a−1). The CaCO3 would dissolve within a few 100 m depth below the saturation horizon, and the dissolution products would enter the mixed layer within a few years to decades, facilitating further absorption of CO2 from the atmosphere. This absorption of CO2 would largely offset the increase in mixed layer pH and carbonate supersaturation resulting from the upwelling of dissolved limestone powder. However, if done on a large scale, the reduction in atmospheric CO2 due to absorption of CO2 by the ocean would reduce the amount of CO2 that needs to be absorbed by the mixed layer, thereby allowing a larger net increase in pH and in supersaturation in the regions receiving CaCO3. At the same time, the reduction in atmospheric pCO2 would cause outgassing of CO2 from ocean regions not subject to addition of CaCO3, thereby increasing the pH and supersaturation in these regions as well. Geographically optimal application of 4 billion t of CaCO3 a−1 (0.48 Gt C a−1) could induce absorption of atmospheric CO2 at a rate of 600 Mt CO2 a−1 after 50 years, 900 Mt CO2 a−1 after 100 years, and 1050 Mt CO2 a−1 after 200 years.
doi_str_mv 10.1029/2007JC004373
format Article
fullrecord <record><control><sourceid>wiley_pasca</sourceid><recordid>TN_cdi_pascalfrancis_primary_20388946</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JGRC10789</sourcerecordid><originalsourceid>FETCH-LOGICAL-i3059-2844a9f0fa92f49eb7011e5da25c43fe2a0ebc50c7e73dfd021c776fc95948723</originalsourceid><addsrcrecordid>eNpNkD1PwzAURS0EElVh4wd4YQw8fySOR4igpSogEAiJxXKd52JIkygOKv33pCqqeMsd7jlvuIScMbhgwPUlB1CzAkAKJQ7IiLM0SzgHfkhGwGSeAOfqmJzG-AnDyTSTwEakuQ99WNo-1EvafyC1_aqJ7Qd2wdHikdNQuw5tHIq6pI1DW1PrQhl8cIPU1HSxobYst3oVVhj7pkbaNusSO9o39LtdY1Vt2w6XAx5PyJG3VcTTvxyT19ubl2KazB8nd8XVPAkCUp3wXEqrPXiruZcaFwoYw7S0PHVSeOQWcOFScAqVKH0JnDmlMu90qmWuuBiT893f1kZnK9_Z2oVo2i6sbLcxHESea5kNnNhx61DhZt8zMNtRzf9RzWzyXDBQuR6sZGeF2OPP3rLdl8mUUKl5e5gYMX1QT_qdmWvxC3lKe3w</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Mitigating the atmospheric CO2 increase and ocean acidification by adding limestone powder to upwelling regions</title><source>Wiley Journals</source><source>Wiley-Blackwell AGU Digital Library</source><source>Wiley Online Library (Open Access Collection)</source><source>Alma/SFX Local Collection</source><creator>Harvey, L. D. D.</creator><creatorcontrib>Harvey, L. D. D.</creatorcontrib><description>The feasibility of enhancing the absorption of CO2 from the atmosphere by adding calcium carbonate (CaCO3) powder to the ocean and of partially reversing the acidification of the ocean and the decrease in calcite supersaturation resulting from the absorption of anthropogenic CO2 is investigated. CaCO3 could be added to the surface layer in regions where the depth of the boundary between supersaturated and unsaturated water is relatively shallow (250–500 m) and where the upwelling velocity is large (30–300 m a−1). The CaCO3 would dissolve within a few 100 m depth below the saturation horizon, and the dissolution products would enter the mixed layer within a few years to decades, facilitating further absorption of CO2 from the atmosphere. This absorption of CO2 would largely offset the increase in mixed layer pH and carbonate supersaturation resulting from the upwelling of dissolved limestone powder. However, if done on a large scale, the reduction in atmospheric CO2 due to absorption of CO2 by the ocean would reduce the amount of CO2 that needs to be absorbed by the mixed layer, thereby allowing a larger net increase in pH and in supersaturation in the regions receiving CaCO3. At the same time, the reduction in atmospheric pCO2 would cause outgassing of CO2 from ocean regions not subject to addition of CaCO3, thereby increasing the pH and supersaturation in these regions as well. Geographically optimal application of 4 billion t of CaCO3 a−1 (0.48 Gt C a−1) could induce absorption of atmospheric CO2 at a rate of 600 Mt CO2 a−1 after 50 years, 900 Mt CO2 a−1 after 100 years, and 1050 Mt CO2 a−1 after 200 years.</description><identifier>ISSN: 0148-0227</identifier><identifier>EISSN: 2156-2202</identifier><identifier>DOI: 10.1029/2007JC004373</identifier><language>eng</language><publisher>Washington, DC: Blackwell Publishing Ltd</publisher><subject>Earth sciences ; Earth, ocean, space ; Exact sciences and technology ; ocean acidification ; ocean carbon sink</subject><ispartof>Journal of Geophysical Research: Oceans, 2008-04, Vol.113 (C4), p.n/a</ispartof><rights>Copyright 2008 by the American Geophysical Union.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1029%2F2007JC004373$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1029%2F2007JC004373$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,11514,27924,27925,45574,45575,46409,46468,46833,46892</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20388946$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Harvey, L. D. D.</creatorcontrib><title>Mitigating the atmospheric CO2 increase and ocean acidification by adding limestone powder to upwelling regions</title><title>Journal of Geophysical Research: Oceans</title><addtitle>J. Geophys. Res</addtitle><description>The feasibility of enhancing the absorption of CO2 from the atmosphere by adding calcium carbonate (CaCO3) powder to the ocean and of partially reversing the acidification of the ocean and the decrease in calcite supersaturation resulting from the absorption of anthropogenic CO2 is investigated. CaCO3 could be added to the surface layer in regions where the depth of the boundary between supersaturated and unsaturated water is relatively shallow (250–500 m) and where the upwelling velocity is large (30–300 m a−1). The CaCO3 would dissolve within a few 100 m depth below the saturation horizon, and the dissolution products would enter the mixed layer within a few years to decades, facilitating further absorption of CO2 from the atmosphere. This absorption of CO2 would largely offset the increase in mixed layer pH and carbonate supersaturation resulting from the upwelling of dissolved limestone powder. However, if done on a large scale, the reduction in atmospheric CO2 due to absorption of CO2 by the ocean would reduce the amount of CO2 that needs to be absorbed by the mixed layer, thereby allowing a larger net increase in pH and in supersaturation in the regions receiving CaCO3. At the same time, the reduction in atmospheric pCO2 would cause outgassing of CO2 from ocean regions not subject to addition of CaCO3, thereby increasing the pH and supersaturation in these regions as well. Geographically optimal application of 4 billion t of CaCO3 a−1 (0.48 Gt C a−1) could induce absorption of atmospheric CO2 at a rate of 600 Mt CO2 a−1 after 50 years, 900 Mt CO2 a−1 after 100 years, and 1050 Mt CO2 a−1 after 200 years.</description><subject>Earth sciences</subject><subject>Earth, ocean, space</subject><subject>Exact sciences and technology</subject><subject>ocean acidification</subject><subject>ocean carbon sink</subject><issn>0148-0227</issn><issn>2156-2202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNpNkD1PwzAURS0EElVh4wd4YQw8fySOR4igpSogEAiJxXKd52JIkygOKv33pCqqeMsd7jlvuIScMbhgwPUlB1CzAkAKJQ7IiLM0SzgHfkhGwGSeAOfqmJzG-AnDyTSTwEakuQ99WNo-1EvafyC1_aqJ7Qd2wdHikdNQuw5tHIq6pI1DW1PrQhl8cIPU1HSxobYst3oVVhj7pkbaNusSO9o39LtdY1Vt2w6XAx5PyJG3VcTTvxyT19ubl2KazB8nd8XVPAkCUp3wXEqrPXiruZcaFwoYw7S0PHVSeOQWcOFScAqVKH0JnDmlMu90qmWuuBiT893f1kZnK9_Z2oVo2i6sbLcxHESea5kNnNhx61DhZt8zMNtRzf9RzWzyXDBQuR6sZGeF2OPP3rLdl8mUUKl5e5gYMX1QT_qdmWvxC3lKe3w</recordid><startdate>200804</startdate><enddate>200804</enddate><creator>Harvey, L. D. D.</creator><general>Blackwell Publishing Ltd</general><general>American Geophysical Union</general><scope>BSCLL</scope><scope>IQODW</scope></search><sort><creationdate>200804</creationdate><title>Mitigating the atmospheric CO2 increase and ocean acidification by adding limestone powder to upwelling regions</title><author>Harvey, L. D. D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3059-2844a9f0fa92f49eb7011e5da25c43fe2a0ebc50c7e73dfd021c776fc95948723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Earth sciences</topic><topic>Earth, ocean, space</topic><topic>Exact sciences and technology</topic><topic>ocean acidification</topic><topic>ocean carbon sink</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harvey, L. D. D.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><jtitle>Journal of Geophysical Research: Oceans</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harvey, L. D. D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitigating the atmospheric CO2 increase and ocean acidification by adding limestone powder to upwelling regions</atitle><jtitle>Journal of Geophysical Research: Oceans</jtitle><addtitle>J. Geophys. Res</addtitle><date>2008-04</date><risdate>2008</risdate><volume>113</volume><issue>C4</issue><epage>n/a</epage><issn>0148-0227</issn><eissn>2156-2202</eissn><abstract>The feasibility of enhancing the absorption of CO2 from the atmosphere by adding calcium carbonate (CaCO3) powder to the ocean and of partially reversing the acidification of the ocean and the decrease in calcite supersaturation resulting from the absorption of anthropogenic CO2 is investigated. CaCO3 could be added to the surface layer in regions where the depth of the boundary between supersaturated and unsaturated water is relatively shallow (250–500 m) and where the upwelling velocity is large (30–300 m a−1). The CaCO3 would dissolve within a few 100 m depth below the saturation horizon, and the dissolution products would enter the mixed layer within a few years to decades, facilitating further absorption of CO2 from the atmosphere. This absorption of CO2 would largely offset the increase in mixed layer pH and carbonate supersaturation resulting from the upwelling of dissolved limestone powder. However, if done on a large scale, the reduction in atmospheric CO2 due to absorption of CO2 by the ocean would reduce the amount of CO2 that needs to be absorbed by the mixed layer, thereby allowing a larger net increase in pH and in supersaturation in the regions receiving CaCO3. At the same time, the reduction in atmospheric pCO2 would cause outgassing of CO2 from ocean regions not subject to addition of CaCO3, thereby increasing the pH and supersaturation in these regions as well. Geographically optimal application of 4 billion t of CaCO3 a−1 (0.48 Gt C a−1) could induce absorption of atmospheric CO2 at a rate of 600 Mt CO2 a−1 after 50 years, 900 Mt CO2 a−1 after 100 years, and 1050 Mt CO2 a−1 after 200 years.</abstract><cop>Washington, DC</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1029/2007JC004373</doi><tpages>21</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0148-0227
ispartof Journal of Geophysical Research: Oceans, 2008-04, Vol.113 (C4), p.n/a
issn 0148-0227
2156-2202
language eng
recordid cdi_pascalfrancis_primary_20388946
source Wiley Journals; Wiley-Blackwell AGU Digital Library; Wiley Online Library (Open Access Collection); Alma/SFX Local Collection
subjects Earth sciences
Earth, ocean, space
Exact sciences and technology
ocean acidification
ocean carbon sink
title Mitigating the atmospheric CO2 increase and ocean acidification by adding limestone powder to upwelling regions
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T09%3A23%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mitigating%20the%20atmospheric%20CO2%20increase%20and%20ocean%20acidification%20by%20adding%20limestone%20powder%20to%20upwelling%20regions&rft.jtitle=Journal%20of%20Geophysical%20Research:%20Oceans&rft.au=Harvey,%20L.%20D.%20D.&rft.date=2008-04&rft.volume=113&rft.issue=C4&rft.epage=n/a&rft.issn=0148-0227&rft.eissn=2156-2202&rft_id=info:doi/10.1029/2007JC004373&rft_dat=%3Cwiley_pasca%3EJGRC10789%3C/wiley_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true