Loading…

The marine carbonate system of the Arctic Ocean: Assessment of internal consistency and sampling considerations, summer 2010

The Arctic Ocean has experienced tremendous changes in recent years. To evaluate temporal and spatial variations of the marine carbonate system, a rigorous evaluation of the quality and internal consistency of Arctic field data and the applicability of existing thermodynamic constants to Arctic cond...

Full description

Saved in:
Bibliographic Details
Published in:Marine chemistry 2015-11, Vol.176, p.174-188
Main Authors: Chen, Baoshan, Cai, Wei-Jun, Chen, Liqi
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73
cites cdi_FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73
container_end_page 188
container_issue
container_start_page 174
container_title Marine chemistry
container_volume 176
creator Chen, Baoshan
Cai, Wei-Jun
Chen, Liqi
description The Arctic Ocean has experienced tremendous changes in recent years. To evaluate temporal and spatial variations of the marine carbonate system, a rigorous evaluation of the quality and internal consistency of Arctic field data and the applicability of existing thermodynamic constants to Arctic conditions is needed. Low Arctic temperatures fall outside the range of conditions used to experimentally determine these constants. Using data collected during the Chinese National Arctic Research Expedition (CHINARE) cruise of summer 2010, we compared underway measurements of the partial pressure of carbon dioxide (pCO2) to pCO2 values calculated using measurements of dissolved inorganic carbon (DIC) and total alkalinity (TAlk) and seven sets of dissociation constants. For waters sampled outside areas of active sea ice melt, calculated and measured pCO2 values agreed best when the calculations incorporated the carbonic acid dissociation constants of Mehrbach et al. (1973) (as refit by Dickson and Millero (1987)) (mean difference of 1.5μatm±standard deviation of 5.7μatm) or Lueker et al. (2000) (2.3±5.4μatm). Differences between calculated and measured pCO2 values were related to temperature and salinity and were, for all sets of constants, increasing with increasing T and S over a temperature range of −1.5 to 10.5°C and a salinity range of 25.8 to 33.1. In the relatively warm Bering Sea, calculated pCO2 was higher than measured pCO2, but in the colder Canada Basin, calculated values were lower than measured values. This pattern indicates that calculations of pCO2 in very cold waters may underestimate pCO2, with an uncertainty of ~5μatm in accuracy. In areas of active sea ice melt (ice cover
doi_str_mv 10.1016/j.marchem.2015.09.007
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1762108146</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0304420315300451</els_id><sourcerecordid>1727673676</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73</originalsourceid><addsrcrecordid>eNqNUcFq3DAQFaGFbNN-QkHHHmJ3JNuSN5ewhCQtBHJJz0KWR40WW95otIGFfny1bO7JaYZ57w0z7zH2XUAtQKif23q2yT3jXEsQXQ3rGkCfsZXotax014tPbAUNtFUroTlnX4i2AKCabr1i_56ekRd5iMidTcMSbUZOB8o488XzXOBNcjk4_ujQxiu-IUKiGWM-4iFmTNFO3C2RQlFFd-A2jpzsvJtC_HsCRkw2h9JdctrPMyZeToWv7LO3E-G3t3rB_tzdPt38qh4e73_fbB4q1-guV6pTg5JOduPgRDfYViP0Ta_9IPworJe9G8G3Wpd5O2gcnBXaraVusPfC6-aC_Tjt3aXlZY-UzRzI4TTZiMuejNBKCuhFqz5AlVrpRukjtTtRXVqIEnqzS6FYeTACzDEYszVvwZhjMAbWpgRTdNcnHZaXXwMmQy4U33AMCV024xLe2fAfHXSa4A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1727673676</pqid></control><display><type>article</type><title>The marine carbonate system of the Arctic Ocean: Assessment of internal consistency and sampling considerations, summer 2010</title><source>ScienceDirect Journals</source><creator>Chen, Baoshan ; Cai, Wei-Jun ; Chen, Liqi</creator><creatorcontrib>Chen, Baoshan ; Cai, Wei-Jun ; Chen, Liqi</creatorcontrib><description>The Arctic Ocean has experienced tremendous changes in recent years. To evaluate temporal and spatial variations of the marine carbonate system, a rigorous evaluation of the quality and internal consistency of Arctic field data and the applicability of existing thermodynamic constants to Arctic conditions is needed. Low Arctic temperatures fall outside the range of conditions used to experimentally determine these constants. Using data collected during the Chinese National Arctic Research Expedition (CHINARE) cruise of summer 2010, we compared underway measurements of the partial pressure of carbon dioxide (pCO2) to pCO2 values calculated using measurements of dissolved inorganic carbon (DIC) and total alkalinity (TAlk) and seven sets of dissociation constants. For waters sampled outside areas of active sea ice melt, calculated and measured pCO2 values agreed best when the calculations incorporated the carbonic acid dissociation constants of Mehrbach et al. (1973) (as refit by Dickson and Millero (1987)) (mean difference of 1.5μatm±standard deviation of 5.7μatm) or Lueker et al. (2000) (2.3±5.4μatm). Differences between calculated and measured pCO2 values were related to temperature and salinity and were, for all sets of constants, increasing with increasing T and S over a temperature range of −1.5 to 10.5°C and a salinity range of 25.8 to 33.1. In the relatively warm Bering Sea, calculated pCO2 was higher than measured pCO2, but in the colder Canada Basin, calculated values were lower than measured values. This pattern indicates that calculations of pCO2 in very cold waters may underestimate pCO2, with an uncertainty of ~5μatm in accuracy. In areas of active sea ice melt (ice cover &lt;35%), large differences between calculated and measured pCO2 values occurred. We explored possible explanations for these large differences and concluded that dissolution of CaCO3 precipitates from sea ice in samples is the most likely cause. Further research including a comparison of filtered and unfiltered samples is needed to resolve this issue. Many processes influence the marine carbonate system of the Arctic Ocean, and further assessment of their relative roles is needed. •We evaluate the internal consistency of the CO2 system through pCO2, DIC, and TAlk in the Arctic Ocean•Mehrbach et al. (1973) as refit by Dickson and Millero (1987), and Lueker et al. (2000) are recommended in the Arctic•Calculated pCO2 values from DIC and TAlk are about 5µatm underestimated in the cold Arctic waters•Potential sampling artifacts are discussed to explore the cause of disagreement between calculated and measured pCO2 values</description><identifier>ISSN: 0304-4203</identifier><identifier>EISSN: 1872-7581</identifier><identifier>DOI: 10.1016/j.marchem.2015.09.007</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Arctic Ocean ; Assessments ; Carbon dioxide ; Carbonates ; Constants ; Dissociation constants ; Dissolution ; Marine ; Mathematical analysis ; Oceanography ; Polar waters ; Sea ice</subject><ispartof>Marine chemistry, 2015-11, Vol.176, p.174-188</ispartof><rights>2015 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73</citedby><cites>FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73</cites><orcidid>0000-0003-3606-8325</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Chen, Baoshan</creatorcontrib><creatorcontrib>Cai, Wei-Jun</creatorcontrib><creatorcontrib>Chen, Liqi</creatorcontrib><title>The marine carbonate system of the Arctic Ocean: Assessment of internal consistency and sampling considerations, summer 2010</title><title>Marine chemistry</title><description>The Arctic Ocean has experienced tremendous changes in recent years. To evaluate temporal and spatial variations of the marine carbonate system, a rigorous evaluation of the quality and internal consistency of Arctic field data and the applicability of existing thermodynamic constants to Arctic conditions is needed. Low Arctic temperatures fall outside the range of conditions used to experimentally determine these constants. Using data collected during the Chinese National Arctic Research Expedition (CHINARE) cruise of summer 2010, we compared underway measurements of the partial pressure of carbon dioxide (pCO2) to pCO2 values calculated using measurements of dissolved inorganic carbon (DIC) and total alkalinity (TAlk) and seven sets of dissociation constants. For waters sampled outside areas of active sea ice melt, calculated and measured pCO2 values agreed best when the calculations incorporated the carbonic acid dissociation constants of Mehrbach et al. (1973) (as refit by Dickson and Millero (1987)) (mean difference of 1.5μatm±standard deviation of 5.7μatm) or Lueker et al. (2000) (2.3±5.4μatm). Differences between calculated and measured pCO2 values were related to temperature and salinity and were, for all sets of constants, increasing with increasing T and S over a temperature range of −1.5 to 10.5°C and a salinity range of 25.8 to 33.1. In the relatively warm Bering Sea, calculated pCO2 was higher than measured pCO2, but in the colder Canada Basin, calculated values were lower than measured values. This pattern indicates that calculations of pCO2 in very cold waters may underestimate pCO2, with an uncertainty of ~5μatm in accuracy. In areas of active sea ice melt (ice cover &lt;35%), large differences between calculated and measured pCO2 values occurred. We explored possible explanations for these large differences and concluded that dissolution of CaCO3 precipitates from sea ice in samples is the most likely cause. Further research including a comparison of filtered and unfiltered samples is needed to resolve this issue. Many processes influence the marine carbonate system of the Arctic Ocean, and further assessment of their relative roles is needed. •We evaluate the internal consistency of the CO2 system through pCO2, DIC, and TAlk in the Arctic Ocean•Mehrbach et al. (1973) as refit by Dickson and Millero (1987), and Lueker et al. (2000) are recommended in the Arctic•Calculated pCO2 values from DIC and TAlk are about 5µatm underestimated in the cold Arctic waters•Potential sampling artifacts are discussed to explore the cause of disagreement between calculated and measured pCO2 values</description><subject>Arctic Ocean</subject><subject>Assessments</subject><subject>Carbon dioxide</subject><subject>Carbonates</subject><subject>Constants</subject><subject>Dissociation constants</subject><subject>Dissolution</subject><subject>Marine</subject><subject>Mathematical analysis</subject><subject>Oceanography</subject><subject>Polar waters</subject><subject>Sea ice</subject><issn>0304-4203</issn><issn>1872-7581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNUcFq3DAQFaGFbNN-QkHHHmJ3JNuSN5ewhCQtBHJJz0KWR40WW95otIGFfny1bO7JaYZ57w0z7zH2XUAtQKif23q2yT3jXEsQXQ3rGkCfsZXotax014tPbAUNtFUroTlnX4i2AKCabr1i_56ekRd5iMidTcMSbUZOB8o488XzXOBNcjk4_ujQxiu-IUKiGWM-4iFmTNFO3C2RQlFFd-A2jpzsvJtC_HsCRkw2h9JdctrPMyZeToWv7LO3E-G3t3rB_tzdPt38qh4e73_fbB4q1-guV6pTg5JOduPgRDfYViP0Ta_9IPworJe9G8G3Wpd5O2gcnBXaraVusPfC6-aC_Tjt3aXlZY-UzRzI4TTZiMuejNBKCuhFqz5AlVrpRukjtTtRXVqIEnqzS6FYeTACzDEYszVvwZhjMAbWpgRTdNcnHZaXXwMmQy4U33AMCV024xLe2fAfHXSa4A</recordid><startdate>20151120</startdate><enddate>20151120</enddate><creator>Chen, Baoshan</creator><creator>Cai, Wei-Jun</creator><creator>Chen, Liqi</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7TN</scope><scope>F1W</scope><scope>H96</scope><scope>L.G</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope><orcidid>https://orcid.org/0000-0003-3606-8325</orcidid></search><sort><creationdate>20151120</creationdate><title>The marine carbonate system of the Arctic Ocean: Assessment of internal consistency and sampling considerations, summer 2010</title><author>Chen, Baoshan ; Cai, Wei-Jun ; Chen, Liqi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Arctic Ocean</topic><topic>Assessments</topic><topic>Carbon dioxide</topic><topic>Carbonates</topic><topic>Constants</topic><topic>Dissociation constants</topic><topic>Dissolution</topic><topic>Marine</topic><topic>Mathematical analysis</topic><topic>Oceanography</topic><topic>Polar waters</topic><topic>Sea ice</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Baoshan</creatorcontrib><creatorcontrib>Cai, Wei-Jun</creatorcontrib><creatorcontrib>Chen, Liqi</creatorcontrib><collection>CrossRef</collection><collection>Oceanic Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy &amp; Non-Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Marine chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Baoshan</au><au>Cai, Wei-Jun</au><au>Chen, Liqi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The marine carbonate system of the Arctic Ocean: Assessment of internal consistency and sampling considerations, summer 2010</atitle><jtitle>Marine chemistry</jtitle><date>2015-11-20</date><risdate>2015</risdate><volume>176</volume><spage>174</spage><epage>188</epage><pages>174-188</pages><issn>0304-4203</issn><eissn>1872-7581</eissn><abstract>The Arctic Ocean has experienced tremendous changes in recent years. To evaluate temporal and spatial variations of the marine carbonate system, a rigorous evaluation of the quality and internal consistency of Arctic field data and the applicability of existing thermodynamic constants to Arctic conditions is needed. Low Arctic temperatures fall outside the range of conditions used to experimentally determine these constants. Using data collected during the Chinese National Arctic Research Expedition (CHINARE) cruise of summer 2010, we compared underway measurements of the partial pressure of carbon dioxide (pCO2) to pCO2 values calculated using measurements of dissolved inorganic carbon (DIC) and total alkalinity (TAlk) and seven sets of dissociation constants. For waters sampled outside areas of active sea ice melt, calculated and measured pCO2 values agreed best when the calculations incorporated the carbonic acid dissociation constants of Mehrbach et al. (1973) (as refit by Dickson and Millero (1987)) (mean difference of 1.5μatm±standard deviation of 5.7μatm) or Lueker et al. (2000) (2.3±5.4μatm). Differences between calculated and measured pCO2 values were related to temperature and salinity and were, for all sets of constants, increasing with increasing T and S over a temperature range of −1.5 to 10.5°C and a salinity range of 25.8 to 33.1. In the relatively warm Bering Sea, calculated pCO2 was higher than measured pCO2, but in the colder Canada Basin, calculated values were lower than measured values. This pattern indicates that calculations of pCO2 in very cold waters may underestimate pCO2, with an uncertainty of ~5μatm in accuracy. In areas of active sea ice melt (ice cover &lt;35%), large differences between calculated and measured pCO2 values occurred. We explored possible explanations for these large differences and concluded that dissolution of CaCO3 precipitates from sea ice in samples is the most likely cause. Further research including a comparison of filtered and unfiltered samples is needed to resolve this issue. Many processes influence the marine carbonate system of the Arctic Ocean, and further assessment of their relative roles is needed. •We evaluate the internal consistency of the CO2 system through pCO2, DIC, and TAlk in the Arctic Ocean•Mehrbach et al. (1973) as refit by Dickson and Millero (1987), and Lueker et al. (2000) are recommended in the Arctic•Calculated pCO2 values from DIC and TAlk are about 5µatm underestimated in the cold Arctic waters•Potential sampling artifacts are discussed to explore the cause of disagreement between calculated and measured pCO2 values</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.marchem.2015.09.007</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-3606-8325</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0304-4203
ispartof Marine chemistry, 2015-11, Vol.176, p.174-188
issn 0304-4203
1872-7581
language eng
recordid cdi_proquest_miscellaneous_1762108146
source ScienceDirect Journals
subjects Arctic Ocean
Assessments
Carbon dioxide
Carbonates
Constants
Dissociation constants
Dissolution
Marine
Mathematical analysis
Oceanography
Polar waters
Sea ice
title The marine carbonate system of the Arctic Ocean: Assessment of internal consistency and sampling considerations, summer 2010
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T17%3A14%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20marine%20carbonate%20system%20of%20the%20Arctic%20Ocean:%20Assessment%20of%20internal%20consistency%20and%20sampling%20considerations,%20summer%202010&rft.jtitle=Marine%20chemistry&rft.au=Chen,%20Baoshan&rft.date=2015-11-20&rft.volume=176&rft.spage=174&rft.epage=188&rft.pages=174-188&rft.issn=0304-4203&rft.eissn=1872-7581&rft_id=info:doi/10.1016/j.marchem.2015.09.007&rft_dat=%3Cproquest_cross%3E1727673676%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c375t-656b62c25dbc15ba47e08387fb1fd1af28cd0f4777e04b7ebca17c9273e8f1f73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1727673676&rft_id=info:pmid/&rfr_iscdi=true