Impact of phosphorus mineral source (Al-P or Fe-P) and pH on cluster-root formation and carboxylate exudation in Lupinus albus L
Lupinus albus L. were grown in rhizoboxes containing a soil amended with sparingly available Fe-P or Al-P (100 μg P g-¹ soil/resin mixture). Root halves of individual plants were supplied with nutrient solution (minus P) buffered at either pH 5.5 or 7.5, to assess whether the source of mineral-bound...
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description | Lupinus albus L. were grown in rhizoboxes containing a soil amended with sparingly available Fe-P or Al-P (100 μg P g-¹ soil/resin mixture). Root halves of individual plants were supplied with nutrient solution (minus P) buffered at either pH 5.5 or 7.5, to assess whether the source of mineral-bound P and/or pH influence cluster-root growth and carboxylate exudation. The P-amended soil was mixed 3:1 (w/w) with anion-exchange resins to allow rapid fixation of carboxylates. Treatments lasted 10 weeks. Forty percent and 30% of the root mass developed as cluster roots in plants grown on Fe-P and Al-P respectively, but cluster-root growth was the same on root-halves grown at pH 5.5 or 7.5. Mineral-bound P source (Al- or Fe-P) had no influence on the types of carboxylates measured in soil associated with cluster roots--citrate (and trace amounts of malate and fumarate) was the only major carboxylate detected. The [citrate] in the rhizosphere of cluster roots decreased with increased shoot P status (suggesting a systemic effect) and also, only for plants grown on Al-P, with decreased pH in the root environment (suggesting a local effect). In a separate experiment using anion exchange resins pre-loaded with malate or citrate, we measured malate (50%) and citrate (79%) recovery after 30 days in soil. We therefore, also conclude that measurements of [citrate] and [malate] at the root surface may be underestimated and would be greater than the 40- and 1.6-μmol g-¹ root DM, respectively estimated by us and others because of decomposition of carboxylates around roots prior to sampling. |
doi_str_mv | 10.1007/s11104-007-9535-7 |
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W ; Lambers, H ; Cawthray, G. R ; Kuhn, A. J ; Schurr, U</creator><creatorcontrib>Shane, M. W ; Lambers, H ; Cawthray, G. R ; Kuhn, A. J ; Schurr, U</creatorcontrib><description>Lupinus albus L. were grown in rhizoboxes containing a soil amended with sparingly available Fe-P or Al-P (100 μg P g-¹ soil/resin mixture). Root halves of individual plants were supplied with nutrient solution (minus P) buffered at either pH 5.5 or 7.5, to assess whether the source of mineral-bound P and/or pH influence cluster-root growth and carboxylate exudation. The P-amended soil was mixed 3:1 (w/w) with anion-exchange resins to allow rapid fixation of carboxylates. Treatments lasted 10 weeks. Forty percent and 30% of the root mass developed as cluster roots in plants grown on Fe-P and Al-P respectively, but cluster-root growth was the same on root-halves grown at pH 5.5 or 7.5. Mineral-bound P source (Al- or Fe-P) had no influence on the types of carboxylates measured in soil associated with cluster roots--citrate (and trace amounts of malate and fumarate) was the only major carboxylate detected. The [citrate] in the rhizosphere of cluster roots decreased with increased shoot P status (suggesting a systemic effect) and also, only for plants grown on Al-P, with decreased pH in the root environment (suggesting a local effect). In a separate experiment using anion exchange resins pre-loaded with malate or citrate, we measured malate (50%) and citrate (79%) recovery after 30 days in soil. We therefore, also conclude that measurements of [citrate] and [malate] at the root surface may be underestimated and would be greater than the 40- and 1.6-μmol g-¹ root DM, respectively estimated by us and others because of decomposition of carboxylates around roots prior to sampling.</description><identifier>ISSN: 0032-079X</identifier><identifier>EISSN: 1573-5036</identifier><identifier>DOI: 10.1007/s11104-007-9535-7</identifier><identifier>CODEN: PLSOA2</identifier><language>eng</language><publisher>Dordrecht: Dordrecht : Springer Netherlands</publisher><subject>Acid soils ; Agricultural soils ; Agronomy. Soil science and plant productions ; Animal, plant and microbial ecology ; Anion exchange ; Biological and medical sciences ; Biomass ; Biomedical and Life Sciences ; Carboxylates ; Citrate ; Citrates ; Ecology ; Fundamental and applied biological sciences. Psychology ; Geochemistry ; Life Sciences ; Lupinus albus ; Mineralogy ; P-deficiency ; Phosphorus ; Plant growth ; Plant Physiology ; Plant roots ; Plant Sciences ; Plants ; Proteoid roots ; Regular Article ; Resins ; Rhizosphere ; Roots ; Soil amendment ; Soil Science & Conservation ; Soils ; Split-root design ; Systemic signal ; White lupin</subject><ispartof>Plant and soil, 2008-03, Vol.304 (1-2), p.169-178</ispartof><rights>2008 Springer</rights><rights>Springer Science+Business Media B.V. 2007</rights><rights>2008 INIST-CNRS</rights><rights>Springer Science+Business Media B.V. 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c519t-ac40a7d074152bc15df0c7139fc16dd3c77793e0be1aa5f9f56f9d4c7a47e60f3</citedby><cites>FETCH-LOGICAL-c519t-ac40a7d074152bc15df0c7139fc16dd3c77793e0be1aa5f9f56f9d4c7a47e60f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/42951817$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/42951817$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,41488,42557,51319,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20189509$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Shane, M. W</creatorcontrib><creatorcontrib>Lambers, H</creatorcontrib><creatorcontrib>Cawthray, G. R</creatorcontrib><creatorcontrib>Kuhn, A. J</creatorcontrib><creatorcontrib>Schurr, U</creatorcontrib><title>Impact of phosphorus mineral source (Al-P or Fe-P) and pH on cluster-root formation and carboxylate exudation in Lupinus albus L</title><title>Plant and soil</title><addtitle>Plant Soil</addtitle><description>Lupinus albus L. were grown in rhizoboxes containing a soil amended with sparingly available Fe-P or Al-P (100 μg P g-¹ soil/resin mixture). Root halves of individual plants were supplied with nutrient solution (minus P) buffered at either pH 5.5 or 7.5, to assess whether the source of mineral-bound P and/or pH influence cluster-root growth and carboxylate exudation. The P-amended soil was mixed 3:1 (w/w) with anion-exchange resins to allow rapid fixation of carboxylates. Treatments lasted 10 weeks. Forty percent and 30% of the root mass developed as cluster roots in plants grown on Fe-P and Al-P respectively, but cluster-root growth was the same on root-halves grown at pH 5.5 or 7.5. Mineral-bound P source (Al- or Fe-P) had no influence on the types of carboxylates measured in soil associated with cluster roots--citrate (and trace amounts of malate and fumarate) was the only major carboxylate detected. The [citrate] in the rhizosphere of cluster roots decreased with increased shoot P status (suggesting a systemic effect) and also, only for plants grown on Al-P, with decreased pH in the root environment (suggesting a local effect). In a separate experiment using anion exchange resins pre-loaded with malate or citrate, we measured malate (50%) and citrate (79%) recovery after 30 days in soil. We therefore, also conclude that measurements of [citrate] and [malate] at the root surface may be underestimated and would be greater than the 40- and 1.6-μmol g-¹ root DM, respectively estimated by us and others because of decomposition of carboxylates around roots prior to sampling.</description><subject>Acid soils</subject><subject>Agricultural soils</subject><subject>Agronomy. Soil science and plant productions</subject><subject>Animal, plant and microbial ecology</subject><subject>Anion exchange</subject><subject>Biological and medical sciences</subject><subject>Biomass</subject><subject>Biomedical and Life Sciences</subject><subject>Carboxylates</subject><subject>Citrate</subject><subject>Citrates</subject><subject>Ecology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Geochemistry</subject><subject>Life Sciences</subject><subject>Lupinus albus</subject><subject>Mineralogy</subject><subject>P-deficiency</subject><subject>Phosphorus</subject><subject>Plant growth</subject><subject>Plant Physiology</subject><subject>Plant roots</subject><subject>Plant Sciences</subject><subject>Plants</subject><subject>Proteoid roots</subject><subject>Regular Article</subject><subject>Resins</subject><subject>Rhizosphere</subject><subject>Roots</subject><subject>Soil amendment</subject><subject>Soil Science & Conservation</subject><subject>Soils</subject><subject>Split-root design</subject><subject>Systemic signal</subject><subject>White lupin</subject><issn>0032-079X</issn><issn>1573-5036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</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>eNqNkV9r1jAUxos48HX6AbwQg7ChF9GTpmmayzHcH3hhgznwLpw3TWZf0qYmLWx3fnRTOiZ4IbtIcpLnd56T5BTFOwZfGID8mhhjUNEcUiW4oPJFsWFCciqA1y-LDQAvKUj141XxOqU9LHtWb4rfl_2IZiLBkfFnSHnEOZG-G2xET1KYo7Hk04mn1yREcmbp9WeCQ0vGCxIGYvycJhtpDGEiLsQepy4fL4DBuAv3Dx4nS-z93K5KN5DtPHZDroF-l-ftm-LAoU_27eN6WNyefft-ekG3V-eXpydbagRTE0VTAcoWZMVEuTNMtA6MZFw5w-q25UZKqbiFnWWIwiknaqfaykispK3B8cPiePUdY_g12zTpvkvGeo-DDXPSJdRlJSQ8C-RQNhn8-A-4z9815EdkBuqqroXIEFshE0NK0To9xq7H-KAZ6KVzeu2cXsKlc1rmnKNHY0wGvYs4mC49JZbAGiVAZa5cuZSl4c7Gvxf4n_n7NWmfphCfTKtSCdawRf-w6g6DxruYC9_e5JIcoBGNbCr-B0cnuxw</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Shane, M. 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Psychology</topic><topic>Geochemistry</topic><topic>Life Sciences</topic><topic>Lupinus albus</topic><topic>Mineralogy</topic><topic>P-deficiency</topic><topic>Phosphorus</topic><topic>Plant growth</topic><topic>Plant Physiology</topic><topic>Plant roots</topic><topic>Plant Sciences</topic><topic>Plants</topic><topic>Proteoid roots</topic><topic>Regular Article</topic><topic>Resins</topic><topic>Rhizosphere</topic><topic>Roots</topic><topic>Soil amendment</topic><topic>Soil Science & Conservation</topic><topic>Soils</topic><topic>Split-root design</topic><topic>Systemic signal</topic><topic>White lupin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shane, M. W</creatorcontrib><creatorcontrib>Lambers, H</creatorcontrib><creatorcontrib>Cawthray, G. R</creatorcontrib><creatorcontrib>Kuhn, A. 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W</au><au>Lambers, H</au><au>Cawthray, G. R</au><au>Kuhn, A. J</au><au>Schurr, U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of phosphorus mineral source (Al-P or Fe-P) and pH on cluster-root formation and carboxylate exudation in Lupinus albus L</atitle><jtitle>Plant and soil</jtitle><stitle>Plant Soil</stitle><date>2008-03-01</date><risdate>2008</risdate><volume>304</volume><issue>1-2</issue><spage>169</spage><epage>178</epage><pages>169-178</pages><issn>0032-079X</issn><eissn>1573-5036</eissn><coden>PLSOA2</coden><abstract>Lupinus albus L. were grown in rhizoboxes containing a soil amended with sparingly available Fe-P or Al-P (100 μg P g-¹ soil/resin mixture). Root halves of individual plants were supplied with nutrient solution (minus P) buffered at either pH 5.5 or 7.5, to assess whether the source of mineral-bound P and/or pH influence cluster-root growth and carboxylate exudation. The P-amended soil was mixed 3:1 (w/w) with anion-exchange resins to allow rapid fixation of carboxylates. Treatments lasted 10 weeks. Forty percent and 30% of the root mass developed as cluster roots in plants grown on Fe-P and Al-P respectively, but cluster-root growth was the same on root-halves grown at pH 5.5 or 7.5. Mineral-bound P source (Al- or Fe-P) had no influence on the types of carboxylates measured in soil associated with cluster roots--citrate (and trace amounts of malate and fumarate) was the only major carboxylate detected. The [citrate] in the rhizosphere of cluster roots decreased with increased shoot P status (suggesting a systemic effect) and also, only for plants grown on Al-P, with decreased pH in the root environment (suggesting a local effect). In a separate experiment using anion exchange resins pre-loaded with malate or citrate, we measured malate (50%) and citrate (79%) recovery after 30 days in soil. We therefore, also conclude that measurements of [citrate] and [malate] at the root surface may be underestimated and would be greater than the 40- and 1.6-μmol g-¹ root DM, respectively estimated by us and others because of decomposition of carboxylates around roots prior to sampling.</abstract><cop>Dordrecht</cop><pub>Dordrecht : Springer Netherlands</pub><doi>10.1007/s11104-007-9535-7</doi><tpages>10</tpages></addata></record> |
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subjects | Acid soils Agricultural soils Agronomy. Soil science and plant productions Animal, plant and microbial ecology Anion exchange Biological and medical sciences Biomass Biomedical and Life Sciences Carboxylates Citrate Citrates Ecology Fundamental and applied biological sciences. Psychology Geochemistry Life Sciences Lupinus albus Mineralogy P-deficiency Phosphorus Plant growth Plant Physiology Plant roots Plant Sciences Plants Proteoid roots Regular Article Resins Rhizosphere Roots Soil amendment Soil Science & Conservation Soils Split-root design Systemic signal White lupin |
title | Impact of phosphorus mineral source (Al-P or Fe-P) and pH on cluster-root formation and carboxylate exudation in Lupinus albus L |
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