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Low molecular weight organic acid adsorption in forest soils: effects on soil solution concentrations and biodegradation rates
Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för naturvetenskap.
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2003 (Engelska)Ingår i: Soil Biology and Biochemistry, ISSN 0038-0717, E-ISSN 1879-3428, Vol. 35, nr 8, s. 1015-1026Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Low molecular weight (LMW) organic acids are believed to play a key role in many rhizosphere and pedogenic processes; However, their efficiency is likely to depend on their susceptibility to sorption and biodegradation. The sorption characteristics of three organic acids (citrate, oxalate and acetate) and phosphate were examined over the concentration range 0-1000 muM in three coniferous forest soil profiles. Sorption to the soil's solid phase could be adequately described by the Langmuir equation with sorption capacity following the horizon series: B > C > E > O. The strength of anion sorption followed the series: phosphate > oxalate : citrate > acetate. Calculations indicated that between 50 and 95% (0 and E horizons) and > 93% (13 horizons) of these LMW organic acids entering the soil will become sorbed to the solid phase. The amount of organic acids predicted to be present on the solid phase at typical soil solution concentrations ranged from < 1 to 1100 nmol g(-1) yielding adsorbed-to-solution ratios (adsorption coefficients) of between < 0.1 and 3100. In the case of citrate, sorption to the solid phase significantly reduced its biodegradation potential by 35-99% depending upon the degree and type of sorption surface. The findings of this work are discussed in the context of the quantitative effects of adsorption on organic acids, their ecological functions and role in soil forming processes.

Ort, förlag, år, upplaga, sidor
2003. Vol. 35, nr 8, s. 1015-1026
Nationell ämneskategori
Biokemi och molekylärbiologi
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URN: urn:nbn:se:miun:diva-13643DOI: 10.1016/S0038-0717(03)00144-5ISI: 000184666200002Scopus ID: 2-s2.0-0042704858OAI: oai:DiVA.org:miun-13643DiVA, id: diva2:411870
Tillgänglig från: 2011-04-19 Skapad: 2011-04-19 Senast uppdaterad: 2017-12-11Bibliografiskt granskad

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van Hees, P A W

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