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      Phosphorus retention in calcareous soils and the effect of organic matter on its mobility

      research-article
      1 ,
      Geochemical Transactions
      BioMed Central

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          Abstract

          A survey of the interactions between phosphorus (P) species and the components of calcareous soils shows that both surface reactions and precipitation take place, especially in the presence of calcite and limestone. The principal products of these reactions are dicalcium phosphate and octacalcium phosphate, which may interconvert after formation. The role of calcium carbonate in P retention by calcareous soils is, however, significant only at relatively high P concentrations – non-carbonate clays play a more important part at lower concentrations. In the presence of iron oxide particles, occlusion of P frequently occurs in these bodies, especially with forms of the element that are pedogenic in origin. Progressive mineralization and immobilization, often biological in nature, are generally observed when P is added as a fertilizer.

          Manure serves both as a source of subsurface P and an effective mobilizing agent. Blockage of P sorption sites by organic acids, as well as complexation of exchangeable Al and Fe in the soil, are potential causes of this mobilization. Swine and chicken manure are especially rich P sources, largely due the practice of adding the element to the feed of nonruminants. Humic materials, both native and added, appear to increase recovery of Olsen P. In the presence of metal cations, strong complexes between inorganic P and humates are formed. The influence of humic soil amendments on P mobility warrants further investigation.

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          Most cited references138

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          Phosphorus Leaching from Soils Containing Different Phosphorus Concentrations in the Broadbalk Experiment

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            Effect of phosphorus supply on the formation and function of proteoid roots of white lupin (Lupinus albus L.)

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              Characterizing phosphorus in environmental and agricultural samples by 31P nuclear magnetic resonance spectroscopy.

              B Cade (2005)
              Phosphorus nuclear magnetic resonance ((31)P-NMR) spectroscopy has advanced our knowledge of organic phosphorus (P) in soils and environmental samples more than any other technique. This paper reviews the use of (31)P-NMR spectroscopy for soil, water and other environmental samples. The requirements for a successful solid-state or solution (31)P-NMR experiment are described, including experimental set-up, sample preparation, extractants, experimental conditions, and post-experimental processing. Next, the literature on solid-state and solution (31)P-NMR spectroscopy in environmental samples is reviewed, including papers on: methods; P transformations; agricultural, forest and natural ecosystem soil studies; humic acid and particle size separations; manure, compost and sludge studies; and water research, including freshwater, estuary and marine studies. Future research needs are also discussed as well as suggestions to improve results, such as increased standardization among research groups.
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                Author and article information

                Journal
                Geochem Trans
                Geochemical Transactions
                BioMed Central (London )
                1467-4866
                2006
                12 June 2006
                : 7
                : 6
                Affiliations
                [1 ]Department of Chemistry, University of Idaho, Moscow, ID 83844-2343, USA
                Article
                1467-4866-7-6
                10.1186/1467-4866-7-6
                1483820
                16768791
                d61aa2ce-be54-49e5-a05c-3a582db72790
                Copyright © 2006 von Wandruszka; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 2 June 2006
                : 12 June 2006
                Categories
                Research Article

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