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Investigating the dissolution of soil phosphate
Aims The effectiveness of phosphate fertilisers decreases with increasing period of reaction. One explanation for this is that the phosphate (P) has changed its chemical form. Evidence for this is provided by fractionation schemes which include extraction with alkali, followed by extraction with aci...
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Published in: | Plant and soil 2023-09, Vol.490 (1-2), p.591-599 |
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container_title | Plant and soil |
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creator | Barrow, N. J. Debnath, Abhijit Sen, Arup |
description | Aims
The effectiveness of phosphate fertilisers decreases with increasing period of reaction. One explanation for this is that the phosphate (P) has changed its chemical form. Evidence for this is provided by fractionation schemes which include extraction with alkali, followed by extraction with acid. Our aim was to test whether alkali and acid extracted different moieties and to test their ability to reflect changes in phosphate form over time.
Methods
We measured the effect of period of reaction between P and an iron (hydroxy)oxide (goethite), an aluminium oxide, and a soil, using two methods. These are: extraction with acid and extraction with alkali.
Results
Extraction of P by acid was similar to extraction by alkali. This is not consistent with the idea that they extract different kinds of phosphate. With increasing period of reaction, more iron and more aluminium needed to be dissolved in order to dissolve the same amount of P. The rate of dissolution of iron and of aluminium decreased with increasing period of reaction with phosphate.
Conclusions
Our results are consistent with diffusion of P into the reacting materials rather than formation of different chemical forms. We think the increased resistance to disolution occurred because phosphate diffused into defects and repaired them. Fractionation methods reflect increasing vigour of extraction rather than the presence of separate forms. |
doi_str_mv | 10.1007/s11104-023-06102-7 |
format | article |
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The effectiveness of phosphate fertilisers decreases with increasing period of reaction. One explanation for this is that the phosphate (P) has changed its chemical form. Evidence for this is provided by fractionation schemes which include extraction with alkali, followed by extraction with acid. Our aim was to test whether alkali and acid extracted different moieties and to test their ability to reflect changes in phosphate form over time.
Methods
We measured the effect of period of reaction between P and an iron (hydroxy)oxide (goethite), an aluminium oxide, and a soil, using two methods. These are: extraction with acid and extraction with alkali.
Results
Extraction of P by acid was similar to extraction by alkali. This is not consistent with the idea that they extract different kinds of phosphate. With increasing period of reaction, more iron and more aluminium needed to be dissolved in order to dissolve the same amount of P. The rate of dissolution of iron and of aluminium decreased with increasing period of reaction with phosphate.
Conclusions
Our results are consistent with diffusion of P into the reacting materials rather than formation of different chemical forms. We think the increased resistance to disolution occurred because phosphate diffused into defects and repaired them. Fractionation methods reflect increasing vigour of extraction rather than the presence of separate forms.</description><identifier>ISSN: 0032-079X</identifier><identifier>EISSN: 1573-5036</identifier><identifier>DOI: 10.1007/s11104-023-06102-7</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Acids ; Agriculture ; Aluminum ; Aluminum oxide ; Biomedical and Life Sciences ; Dissolution ; Ecology ; Fractionation ; Goethite ; Iron ; Life Sciences ; Phosphate ; Phosphates ; Plant Physiology ; Plant Sciences ; Research Article ; Soil Science & Conservation ; Soils</subject><ispartof>Plant and soil, 2023-09, Vol.490 (1-2), p.591-599</ispartof><rights>The Author(s) 2023. corrected publication 2023</rights><rights>The Author(s) 2023. corrected publication 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-8dec12ceb205aa50c36232f0de38607ec8dbcc8b2ba3c7dc6744373773b37de3</citedby><cites>FETCH-LOGICAL-c363t-8dec12ceb205aa50c36232f0de38607ec8dbcc8b2ba3c7dc6744373773b37de3</cites><orcidid>0000-0002-7695-5351</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>Barrow, N. J.</creatorcontrib><creatorcontrib>Debnath, Abhijit</creatorcontrib><creatorcontrib>Sen, Arup</creatorcontrib><title>Investigating the dissolution of soil phosphate</title><title>Plant and soil</title><addtitle>Plant Soil</addtitle><description>Aims
The effectiveness of phosphate fertilisers decreases with increasing period of reaction. One explanation for this is that the phosphate (P) has changed its chemical form. Evidence for this is provided by fractionation schemes which include extraction with alkali, followed by extraction with acid. Our aim was to test whether alkali and acid extracted different moieties and to test their ability to reflect changes in phosphate form over time.
Methods
We measured the effect of period of reaction between P and an iron (hydroxy)oxide (goethite), an aluminium oxide, and a soil, using two methods. These are: extraction with acid and extraction with alkali.
Results
Extraction of P by acid was similar to extraction by alkali. This is not consistent with the idea that they extract different kinds of phosphate. With increasing period of reaction, more iron and more aluminium needed to be dissolved in order to dissolve the same amount of P. The rate of dissolution of iron and of aluminium decreased with increasing period of reaction with phosphate.
Conclusions
Our results are consistent with diffusion of P into the reacting materials rather than formation of different chemical forms. We think the increased resistance to disolution occurred because phosphate diffused into defects and repaired them. Fractionation methods reflect increasing vigour of extraction rather than the presence of separate forms.</description><subject>Acids</subject><subject>Agriculture</subject><subject>Aluminum</subject><subject>Aluminum oxide</subject><subject>Biomedical and Life Sciences</subject><subject>Dissolution</subject><subject>Ecology</subject><subject>Fractionation</subject><subject>Goethite</subject><subject>Iron</subject><subject>Life Sciences</subject><subject>Phosphate</subject><subject>Phosphates</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Research Article</subject><subject>Soil Science & Conservation</subject><subject>Soils</subject><issn>0032-079X</issn><issn>1573-5036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMouK7-AU8Fz3EnmTZpj7L4sbDgZQ_eQpqmH0ttatIK_nuzVvDmKUx43neGh5BbBvcMQG4CYwxSChwpCAacyjOyYplEmgGKc7ICQE5BFm-X5CqEI5xmJlZksxs-bZi6Rk_d0CRTa5OqC8H189S5IXF1ElzXJ2PrwtjqyV6Ti1r3wd78vmtyeHo8bF_o_vV5t33YU4MCJ5pX1jBubMkh0zqD-MuR11BZzAVIa_KqNCYveanRyMoImaYoUUosUUZoTe6W2tG7jzkeqI5u9kPcqHguiliCWREpvlDGuxC8rdXou3ftvxQDdfKiFi8qelE_XpSMIVxCIcJDY_1f9T-pbwZ7ZVw</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Barrow, N. 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J. ; Debnath, Abhijit ; Sen, Arup</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-8dec12ceb205aa50c36232f0de38607ec8dbcc8b2ba3c7dc6744373773b37de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acids</topic><topic>Agriculture</topic><topic>Aluminum</topic><topic>Aluminum oxide</topic><topic>Biomedical and Life Sciences</topic><topic>Dissolution</topic><topic>Ecology</topic><topic>Fractionation</topic><topic>Goethite</topic><topic>Iron</topic><topic>Life Sciences</topic><topic>Phosphate</topic><topic>Phosphates</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Research Article</topic><topic>Soil Science & Conservation</topic><topic>Soils</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barrow, N. J.</creatorcontrib><creatorcontrib>Debnath, Abhijit</creatorcontrib><creatorcontrib>Sen, Arup</creatorcontrib><collection>SpringerOpen website</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Agricultural Science Collection</collection><collection>Biology Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Plant and soil</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barrow, N. J.</au><au>Debnath, Abhijit</au><au>Sen, Arup</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigating the dissolution of soil phosphate</atitle><jtitle>Plant and soil</jtitle><stitle>Plant Soil</stitle><date>2023-09-01</date><risdate>2023</risdate><volume>490</volume><issue>1-2</issue><spage>591</spage><epage>599</epage><pages>591-599</pages><issn>0032-079X</issn><eissn>1573-5036</eissn><abstract>Aims
The effectiveness of phosphate fertilisers decreases with increasing period of reaction. One explanation for this is that the phosphate (P) has changed its chemical form. Evidence for this is provided by fractionation schemes which include extraction with alkali, followed by extraction with acid. Our aim was to test whether alkali and acid extracted different moieties and to test their ability to reflect changes in phosphate form over time.
Methods
We measured the effect of period of reaction between P and an iron (hydroxy)oxide (goethite), an aluminium oxide, and a soil, using two methods. These are: extraction with acid and extraction with alkali.
Results
Extraction of P by acid was similar to extraction by alkali. This is not consistent with the idea that they extract different kinds of phosphate. With increasing period of reaction, more iron and more aluminium needed to be dissolved in order to dissolve the same amount of P. The rate of dissolution of iron and of aluminium decreased with increasing period of reaction with phosphate.
Conclusions
Our results are consistent with diffusion of P into the reacting materials rather than formation of different chemical forms. We think the increased resistance to disolution occurred because phosphate diffused into defects and repaired them. Fractionation methods reflect increasing vigour of extraction rather than the presence of separate forms.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s11104-023-06102-7</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7695-5351</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acids Agriculture Aluminum Aluminum oxide Biomedical and Life Sciences Dissolution Ecology Fractionation Goethite Iron Life Sciences Phosphate Phosphates Plant Physiology Plant Sciences Research Article Soil Science & Conservation Soils |
title | Investigating the dissolution of soil phosphate |
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