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Coupling primary production and terrestrial runoff to ocean acidification and carbonate mineral suppression in the eastern Bering Sea
Water column pH and carbonate mineral saturation states were calculated from dissolved inorganic carbon (DIC) and total alkalinity data collected over the eastern Bering Sea shelf in the spring and summer of 2008. The saturation states (Ω) of the two most important carbonate minerals, calcite (Ωcalc...
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Published in: | Journal of Geophysical Research 2011-02, Vol.116 (C2), p.n/a, Article C02030 |
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description | Water column pH and carbonate mineral saturation states were calculated from dissolved inorganic carbon (DIC) and total alkalinity data collected over the eastern Bering Sea shelf in the spring and summer of 2008. The saturation states (Ω) of the two most important carbonate minerals, calcite (Ωcalcite) and aragonite (Ωaragonite) were strongly coupled to terrestrial runoff from the Yukon and Kuskokwim rivers, primary production in the surface waters, and remineralization of organic matter at depth over the shelf. In spring, before ice melt occurred, pH over the shelf was largely confined to a range of 7.9–8.1 and Ωcalcite and Ωaragonite ranged from 1.5 to 3.0 and 0.8 to 2.0, respectively. At the stations closest to river outflows, aragonite was undersaturated in the water column from the surface to the bottom. During the summer sea ice retreat, high rates of primary production consumed DIC in the mixed layer, which increased pH and Ωcalcite and Ωaragonite. However, Ωcalcite and Ωaragonite decreased by ∼0.3 in the bottom waters over the middle and outer shelf. Over the northern shelf, where export production is highest, Ωaragonite decreased by ∼0.35 and became highly undersaturated. The observed suppression and undersaturation of Ωcalcite and Ωaragonite in the eastern Bering Sea are correlated with anthropogenic carbon dioxide uptake into the ocean and will likely be exacerbated under business‐as‐usual emission scenarios. Therefore, ocean acidification could threaten some benthic and pelagic calcifying organisms across the Bering Sea shelf in the coming decades. |
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The saturation states (Ω) of the two most important carbonate minerals, calcite (Ωcalcite) and aragonite (Ωaragonite) were strongly coupled to terrestrial runoff from the Yukon and Kuskokwim rivers, primary production in the surface waters, and remineralization of organic matter at depth over the shelf. In spring, before ice melt occurred, pH over the shelf was largely confined to a range of 7.9–8.1 and Ωcalcite and Ωaragonite ranged from 1.5 to 3.0 and 0.8 to 2.0, respectively. At the stations closest to river outflows, aragonite was undersaturated in the water column from the surface to the bottom. During the summer sea ice retreat, high rates of primary production consumed DIC in the mixed layer, which increased pH and Ωcalcite and Ωaragonite. However, Ωcalcite and Ωaragonite decreased by ∼0.3 in the bottom waters over the middle and outer shelf. Over the northern shelf, where export production is highest, Ωaragonite decreased by ∼0.35 and became highly undersaturated. The observed suppression and undersaturation of Ωcalcite and Ωaragonite in the eastern Bering Sea are correlated with anthropogenic carbon dioxide uptake into the ocean and will likely be exacerbated under business‐as‐usual emission scenarios. Therefore, ocean acidification could threaten some benthic and pelagic calcifying organisms across the Bering Sea shelf in the coming decades.</description><identifier>ISSN: 0148-0227</identifier><identifier>ISSN: 2169-9275</identifier><identifier>EISSN: 2156-2202</identifier><identifier>EISSN: 2169-9291</identifier><identifier>DOI: 10.1029/2010JC006453</identifier><language>eng</language><publisher>Washington: Blackwell Publishing Ltd</publisher><subject>Acidification ; Alkalinity ; Anthropogenic factors ; Bering Sea ; Biological oceanography ; Calcite ; carbon biogeochemistry ; Carbon dioxide ; carbonate mineral saturation states ; Chemical oceanography ; Climate change ; Cryosphere ; Dissolved inorganic carbon ; Earth ; Geophysics ; Marine ; Ocean acidification ; Oceans ; Organic matter ; Primary production ; Rivers ; Runoff ; Sea ice ; Seawater ; Spring ; Summer ; Surface water ; Water column</subject><ispartof>Journal of Geophysical Research, 2011-02, Vol.116 (C2), p.n/a, Article C02030</ispartof><rights>Copyright 2011 by the American Geophysical Union.</rights><rights>Copyright 2011 by American Geophysical Union</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a5741-f1dc8544a81f78eb2234c39ff7497bdf006095e6a9460bfce0d660e511315a6a3</citedby><cites>FETCH-LOGICAL-a5741-f1dc8544a81f78eb2234c39ff7497bdf006095e6a9460bfce0d660e511315a6a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1029%2F2010JC006453$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1029%2F2010JC006453$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,11514,27924,27925,46468,46892</link.rule.ids></links><search><creatorcontrib>Mathis, Jeremy T.</creatorcontrib><creatorcontrib>Cross, Jessica N.</creatorcontrib><creatorcontrib>Bates, Nicholas R.</creatorcontrib><title>Coupling primary production and terrestrial runoff to ocean acidification and carbonate mineral suppression in the eastern Bering Sea</title><title>Journal of Geophysical Research</title><addtitle>J. Geophys. Res</addtitle><description>Water column pH and carbonate mineral saturation states were calculated from dissolved inorganic carbon (DIC) and total alkalinity data collected over the eastern Bering Sea shelf in the spring and summer of 2008. The saturation states (Ω) of the two most important carbonate minerals, calcite (Ωcalcite) and aragonite (Ωaragonite) were strongly coupled to terrestrial runoff from the Yukon and Kuskokwim rivers, primary production in the surface waters, and remineralization of organic matter at depth over the shelf. In spring, before ice melt occurred, pH over the shelf was largely confined to a range of 7.9–8.1 and Ωcalcite and Ωaragonite ranged from 1.5 to 3.0 and 0.8 to 2.0, respectively. At the stations closest to river outflows, aragonite was undersaturated in the water column from the surface to the bottom. During the summer sea ice retreat, high rates of primary production consumed DIC in the mixed layer, which increased pH and Ωcalcite and Ωaragonite. However, Ωcalcite and Ωaragonite decreased by ∼0.3 in the bottom waters over the middle and outer shelf. Over the northern shelf, where export production is highest, Ωaragonite decreased by ∼0.35 and became highly undersaturated. The observed suppression and undersaturation of Ωcalcite and Ωaragonite in the eastern Bering Sea are correlated with anthropogenic carbon dioxide uptake into the ocean and will likely be exacerbated under business‐as‐usual emission scenarios. Therefore, ocean acidification could threaten some benthic and pelagic calcifying organisms across the Bering Sea shelf in the coming decades.</description><subject>Acidification</subject><subject>Alkalinity</subject><subject>Anthropogenic factors</subject><subject>Bering Sea</subject><subject>Biological oceanography</subject><subject>Calcite</subject><subject>carbon biogeochemistry</subject><subject>Carbon dioxide</subject><subject>carbonate mineral saturation states</subject><subject>Chemical oceanography</subject><subject>Climate change</subject><subject>Cryosphere</subject><subject>Dissolved inorganic carbon</subject><subject>Earth</subject><subject>Geophysics</subject><subject>Marine</subject><subject>Ocean acidification</subject><subject>Oceans</subject><subject>Organic matter</subject><subject>Primary production</subject><subject>Rivers</subject><subject>Runoff</subject><subject>Sea ice</subject><subject>Seawater</subject><subject>Spring</subject><subject>Summer</subject><subject>Surface water</subject><subject>Water column</subject><issn>0148-0227</issn><issn>2169-9275</issn><issn>2156-2202</issn><issn>2169-9291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kU1uFDEQhS0EEqNJdhzAYsWCJv7v9pK0yCRRRJQElKXlcZfBocce7G6RHIB749FEEcoitamFv_dcrwqhd5R8ooTpI0YoOe8JUULyV2jBqFQNY4S9RgtCRdcQxtq36LCUO1JLSCUIXaC_fZq3Y4g_8DaHjc0PtadhdlNIEds44AlyhjLlYEec55i8x1PCyYGt7y4MwQdnn2hn8zpFOwHehAi5asq83VaDsiNCxNNPwGBLdY34GPLu4xuwB-iNt2OBw8e-RN9PvnzrT5uLy9VZ__misbIVtPF0cJ0UwnbUtx2sGePCce19K3S7HnwNT7QEZbVQZO0dkEEpApJSTqVVli_Rh71vDfl7rrHMJhQH42gjpLkYqqnWku9qid4_Q-_SnGOdzmjaKi6U6l6COkW4FKpTFfq4h1xOpWTw5nHVhhKzO535_3QV53v8Txjh4UXWnK-ue0q7mm-Jmr0q1N3eP6ls_mVUy1tpbr-uzPXxydXN6dWtEfwf_eapzw</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Mathis, Jeremy T.</creator><creator>Cross, Jessica N.</creator><creator>Bates, Nicholas R.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TG</scope><scope>7TN</scope><scope>7XB</scope><scope>88I</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>GNUQQ</scope><scope>H96</scope><scope>HCIFZ</scope><scope>KL.</scope><scope>L.G</scope><scope>M2P</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope></search><sort><creationdate>201102</creationdate><title>Coupling primary production and terrestrial runoff to ocean acidification and carbonate mineral suppression in the eastern Bering Sea</title><author>Mathis, Jeremy T. ; Cross, Jessica N. ; Bates, Nicholas R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a5741-f1dc8544a81f78eb2234c39ff7497bdf006095e6a9460bfce0d660e511315a6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acidification</topic><topic>Alkalinity</topic><topic>Anthropogenic factors</topic><topic>Bering Sea</topic><topic>Biological oceanography</topic><topic>Calcite</topic><topic>carbon biogeochemistry</topic><topic>Carbon dioxide</topic><topic>carbonate mineral saturation states</topic><topic>Chemical oceanography</topic><topic>Climate change</topic><topic>Cryosphere</topic><topic>Dissolved inorganic carbon</topic><topic>Earth</topic><topic>Geophysics</topic><topic>Marine</topic><topic>Ocean acidification</topic><topic>Oceans</topic><topic>Organic matter</topic><topic>Primary production</topic><topic>Rivers</topic><topic>Runoff</topic><topic>Sea ice</topic><topic>Seawater</topic><topic>Spring</topic><topic>Summer</topic><topic>Surface water</topic><topic>Water column</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mathis, Jeremy T.</creatorcontrib><creatorcontrib>Cross, Jessica N.</creatorcontrib><creatorcontrib>Bates, Nicholas R.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Oceanic Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ProQuest Central Student</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy & Non-Living Resources</collection><collection>SciTech Premium Collection</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Science Database</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><jtitle>Journal of Geophysical Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mathis, Jeremy T.</au><au>Cross, Jessica N.</au><au>Bates, Nicholas R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coupling primary production and terrestrial runoff to ocean acidification and carbonate mineral suppression in the eastern Bering Sea</atitle><jtitle>Journal of Geophysical Research</jtitle><addtitle>J. Geophys. Res</addtitle><date>2011-02</date><risdate>2011</risdate><volume>116</volume><issue>C2</issue><epage>n/a</epage><artnum>C02030</artnum><issn>0148-0227</issn><issn>2169-9275</issn><eissn>2156-2202</eissn><eissn>2169-9291</eissn><abstract>Water column pH and carbonate mineral saturation states were calculated from dissolved inorganic carbon (DIC) and total alkalinity data collected over the eastern Bering Sea shelf in the spring and summer of 2008. The saturation states (Ω) of the two most important carbonate minerals, calcite (Ωcalcite) and aragonite (Ωaragonite) were strongly coupled to terrestrial runoff from the Yukon and Kuskokwim rivers, primary production in the surface waters, and remineralization of organic matter at depth over the shelf. In spring, before ice melt occurred, pH over the shelf was largely confined to a range of 7.9–8.1 and Ωcalcite and Ωaragonite ranged from 1.5 to 3.0 and 0.8 to 2.0, respectively. At the stations closest to river outflows, aragonite was undersaturated in the water column from the surface to the bottom. During the summer sea ice retreat, high rates of primary production consumed DIC in the mixed layer, which increased pH and Ωcalcite and Ωaragonite. However, Ωcalcite and Ωaragonite decreased by ∼0.3 in the bottom waters over the middle and outer shelf. Over the northern shelf, where export production is highest, Ωaragonite decreased by ∼0.35 and became highly undersaturated. The observed suppression and undersaturation of Ωcalcite and Ωaragonite in the eastern Bering Sea are correlated with anthropogenic carbon dioxide uptake into the ocean and will likely be exacerbated under business‐as‐usual emission scenarios. Therefore, ocean acidification could threaten some benthic and pelagic calcifying organisms across the Bering Sea shelf in the coming decades.</abstract><cop>Washington</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1029/2010JC006453</doi><tpages>24</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acidification Alkalinity Anthropogenic factors Bering Sea Biological oceanography Calcite carbon biogeochemistry Carbon dioxide carbonate mineral saturation states Chemical oceanography Climate change Cryosphere Dissolved inorganic carbon Earth Geophysics Marine Ocean acidification Oceans Organic matter Primary production Rivers Runoff Sea ice Seawater Spring Summer Surface water Water column |
title | Coupling primary production and terrestrial runoff to ocean acidification and carbonate mineral suppression in the eastern Bering Sea |
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