Sensitive determination of enzymatically labile dissolved organic phosphorus and its vertical profiles in the oligotrophic western North Pacific and East China Sea
Trace concentrations of labile dissolved organic phosphorus (LDOP) in oligotrophic seawater were measured by use of an enzymatic procedure and a nanomolar phosphate analytical system consisting of a gas-segmented continuous flow analyzer with a liquid waveguide capillary cell. LDOP, defined as DOP h...
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Veröffentlicht in: | Journal of oceanography 2013-06, Vol.69 (3), p.357-367 |
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creator | Hashihama, Fuminori Kinouchi, Shinko Suwa, Shuhei Suzumura, Masahiro Kanda, Jota |
description | Trace concentrations of labile dissolved organic phosphorus (LDOP) in oligotrophic seawater were measured by use of an enzymatic procedure and a nanomolar phosphate analytical system consisting of a gas-segmented continuous flow analyzer with a liquid waveguide capillary cell. LDOP, defined as DOP hydrolyzed by alkaline phosphatase (AP) from
Escherichia coli
, was quantified as the difference between the phosphate concentrations of the seawater sample with and without AP treatment. For sensitive measurement of LDOP, we found that phosphate contamination derived from commercially available AP must be corrected, and azide treatment before AP treatment proved effective in removing biological effect that occurs during DOP hydrolysis. Field observations at six stations of the western North Pacific and the East China Sea during the boreal summer revealed that, in the upper 200 m of the water column, LDOP concentrations ranged from the detection limit (3 n
M
) to 243 n
M
, and phosphate concentrations ranged from 5 to 374 n
M
. The spatial distribution patterns of LDOP were similar to those of phosphate. Most of the depth profiles for LDOP and phosphate showed concentrations were extremely low, |
doi_str_mv | 10.1007/s10872-013-0178-4 |
format | Article |
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Escherichia coli
, was quantified as the difference between the phosphate concentrations of the seawater sample with and without AP treatment. For sensitive measurement of LDOP, we found that phosphate contamination derived from commercially available AP must be corrected, and azide treatment before AP treatment proved effective in removing biological effect that occurs during DOP hydrolysis. Field observations at six stations of the western North Pacific and the East China Sea during the boreal summer revealed that, in the upper 200 m of the water column, LDOP concentrations ranged from the detection limit (3 n
M
) to 243 n
M
, and phosphate concentrations ranged from 5 to 374 n
M
. The spatial distribution patterns of LDOP were similar to those of phosphate. Most of the depth profiles for LDOP and phosphate showed concentrations were extremely low, <25 n
M
, between the surface and the deep chlorophyll maximum layer (DCML) and increased below the DCML. Strongly depleted LDOP and phosphate above the DCML suggest that LDOP is actively hydrolyzed under phosphate-depleted conditions and utilized by microbes.</description><identifier>ISSN: 0916-8370</identifier><identifier>EISSN: 1573-868X</identifier><identifier>DOI: 10.1007/s10872-013-0178-4</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Biological effects ; Chemical analysis ; Chemical oceanography ; Continuous flow ; Dissolved organic phosphorus ; Distribution patterns ; E coli ; Earth and Environmental Science ; Earth Sciences ; Escherichia coli ; Freshwater & Marine Ecology ; Marine ; Oceanography ; Original Article ; Phosphates ; Phosphorus content ; Seawater ; Spatial distribution ; Water analysis ; Water column</subject><ispartof>Journal of oceanography, 2013-06, Vol.69 (3), p.357-367</ispartof><rights>The Oceanographic Society of Japan and Springer Japan 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-c4a3dc8727b08b0752ab2730fdf45ae879fcd91022440db2a75b8cde7dbe39543</citedby><cites>FETCH-LOGICAL-c442t-c4a3dc8727b08b0752ab2730fdf45ae879fcd91022440db2a75b8cde7dbe39543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10872-013-0178-4$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10872-013-0178-4$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Hashihama, Fuminori</creatorcontrib><creatorcontrib>Kinouchi, Shinko</creatorcontrib><creatorcontrib>Suwa, Shuhei</creatorcontrib><creatorcontrib>Suzumura, Masahiro</creatorcontrib><creatorcontrib>Kanda, Jota</creatorcontrib><title>Sensitive determination of enzymatically labile dissolved organic phosphorus and its vertical profiles in the oligotrophic western North Pacific and East China Sea</title><title>Journal of oceanography</title><addtitle>J Oceanogr</addtitle><description>Trace concentrations of labile dissolved organic phosphorus (LDOP) in oligotrophic seawater were measured by use of an enzymatic procedure and a nanomolar phosphate analytical system consisting of a gas-segmented continuous flow analyzer with a liquid waveguide capillary cell. LDOP, defined as DOP hydrolyzed by alkaline phosphatase (AP) from
Escherichia coli
, was quantified as the difference between the phosphate concentrations of the seawater sample with and without AP treatment. For sensitive measurement of LDOP, we found that phosphate contamination derived from commercially available AP must be corrected, and azide treatment before AP treatment proved effective in removing biological effect that occurs during DOP hydrolysis. Field observations at six stations of the western North Pacific and the East China Sea during the boreal summer revealed that, in the upper 200 m of the water column, LDOP concentrations ranged from the detection limit (3 n
M
) to 243 n
M
, and phosphate concentrations ranged from 5 to 374 n
M
. The spatial distribution patterns of LDOP were similar to those of phosphate. Most of the depth profiles for LDOP and phosphate showed concentrations were extremely low, <25 n
M
, between the surface and the deep chlorophyll maximum layer (DCML) and increased below the DCML. Strongly depleted LDOP and phosphate above the DCML suggest that LDOP is actively hydrolyzed under phosphate-depleted conditions and utilized by microbes.</description><subject>Biological effects</subject><subject>Chemical analysis</subject><subject>Chemical oceanography</subject><subject>Continuous flow</subject><subject>Dissolved organic phosphorus</subject><subject>Distribution patterns</subject><subject>E coli</subject><subject>Earth and Environmental Science</subject><subject>Earth Sciences</subject><subject>Escherichia coli</subject><subject>Freshwater & Marine Ecology</subject><subject>Marine</subject><subject>Oceanography</subject><subject>Original Article</subject><subject>Phosphates</subject><subject>Phosphorus content</subject><subject>Seawater</subject><subject>Spatial distribution</subject><subject>Water analysis</subject><subject>Water column</subject><issn>0916-8370</issn><issn>1573-868X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kcGOFCEURYlxEtsZP8AdiRs3pVBQBbU0nXE0majJjIk7QsGrLiY0tFDdpv2d-VFf2y6MiYsHgZx7ueES8pKzN5wx9bZyplXbMC5wlG7kE7LinRKN7vW3p2TFBt43Wij2jDyv9YExNmglVuTxDlINSzgA9bBA2YZkl5ATzROF9PO4xZOzMR5ptGOISIVaczyAp7lsbAqO7uZcccq-Ups8DUulByi_ZXRX8oSqSkOiyww0x7DJS8m7GYU_oOKLiX7KZZnpF-vChLcnj2tbF7qeMQu9A3tFLiYbK7z4s1-Sr--v79cfmtvPNx_X724bJ2W74GqFd_gLamR6ZKpr7dgqwSY_yc6CVsPk_MBZ20rJ_Nha1Y3aeVB-BDF0UlyS12dfTP19j-HMNlQHMdoEeV8NF72Sg-yZQvTVP-hD3peE6ZDqpOK9EANS_Ey5kmstMJldCVtbjoYzc6rNnGszWJs51WZOIdqzpiKbNlD-cv6v6BfEbJ59</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Hashihama, Fuminori</creator><creator>Kinouchi, Shinko</creator><creator>Suwa, Shuhei</creator><creator>Suzumura, Masahiro</creator><creator>Kanda, Jota</creator><general>Springer Japan</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7ST</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>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>GNUQQ</scope><scope>H96</scope><scope>HCIFZ</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><scope>SOI</scope><scope>7TV</scope></search><sort><creationdate>20130601</creationdate><title>Sensitive determination of enzymatically labile dissolved organic phosphorus and its vertical profiles in the oligotrophic western North Pacific and East China Sea</title><author>Hashihama, Fuminori ; Kinouchi, Shinko ; Suwa, Shuhei ; Suzumura, Masahiro ; Kanda, Jota</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-c4a3dc8727b08b0752ab2730fdf45ae879fcd91022440db2a75b8cde7dbe39543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Biological effects</topic><topic>Chemical analysis</topic><topic>Chemical oceanography</topic><topic>Continuous flow</topic><topic>Dissolved organic phosphorus</topic><topic>Distribution patterns</topic><topic>E coli</topic><topic>Earth and Environmental Science</topic><topic>Earth Sciences</topic><topic>Escherichia coli</topic><topic>Freshwater & Marine Ecology</topic><topic>Marine</topic><topic>Oceanography</topic><topic>Original Article</topic><topic>Phosphates</topic><topic>Phosphorus content</topic><topic>Seawater</topic><topic>Spatial distribution</topic><topic>Water analysis</topic><topic>Water column</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashihama, Fuminori</creatorcontrib><creatorcontrib>Kinouchi, Shinko</creatorcontrib><creatorcontrib>Suwa, Shuhei</creatorcontrib><creatorcontrib>Suzumura, Masahiro</creatorcontrib><creatorcontrib>Kanda, Jota</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Environment 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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>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><collection>Environment Abstracts</collection><collection>Pollution Abstracts</collection><jtitle>Journal of oceanography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashihama, Fuminori</au><au>Kinouchi, Shinko</au><au>Suwa, Shuhei</au><au>Suzumura, Masahiro</au><au>Kanda, Jota</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sensitive determination of enzymatically labile dissolved organic phosphorus and its vertical profiles in the oligotrophic western North Pacific and East China Sea</atitle><jtitle>Journal of oceanography</jtitle><stitle>J Oceanogr</stitle><date>2013-06-01</date><risdate>2013</risdate><volume>69</volume><issue>3</issue><spage>357</spage><epage>367</epage><pages>357-367</pages><issn>0916-8370</issn><eissn>1573-868X</eissn><abstract>Trace concentrations of labile dissolved organic phosphorus (LDOP) in oligotrophic seawater were measured by use of an enzymatic procedure and a nanomolar phosphate analytical system consisting of a gas-segmented continuous flow analyzer with a liquid waveguide capillary cell. LDOP, defined as DOP hydrolyzed by alkaline phosphatase (AP) from
Escherichia coli
, was quantified as the difference between the phosphate concentrations of the seawater sample with and without AP treatment. For sensitive measurement of LDOP, we found that phosphate contamination derived from commercially available AP must be corrected, and azide treatment before AP treatment proved effective in removing biological effect that occurs during DOP hydrolysis. Field observations at six stations of the western North Pacific and the East China Sea during the boreal summer revealed that, in the upper 200 m of the water column, LDOP concentrations ranged from the detection limit (3 n
M
) to 243 n
M
, and phosphate concentrations ranged from 5 to 374 n
M
. The spatial distribution patterns of LDOP were similar to those of phosphate. Most of the depth profiles for LDOP and phosphate showed concentrations were extremely low, <25 n
M
, between the surface and the deep chlorophyll maximum layer (DCML) and increased below the DCML. Strongly depleted LDOP and phosphate above the DCML suggest that LDOP is actively hydrolyzed under phosphate-depleted conditions and utilized by microbes.</abstract><cop>Japan</cop><pub>Springer Japan</pub><doi>10.1007/s10872-013-0178-4</doi><tpages>11</tpages></addata></record> |
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subjects | Biological effects Chemical analysis Chemical oceanography Continuous flow Dissolved organic phosphorus Distribution patterns E coli Earth and Environmental Science Earth Sciences Escherichia coli Freshwater & Marine Ecology Marine Oceanography Original Article Phosphates Phosphorus content Seawater Spatial distribution Water analysis Water column |
title | Sensitive determination of enzymatically labile dissolved organic phosphorus and its vertical profiles in the oligotrophic western North Pacific and East China Sea |
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