Abstract

Soils comprise various heterogeneously distributed pools of lithogenic, free organic, occluded, adsorbed, and precipitated phosphorus (P) forms, which differ depending on soil forming factors. Small-scale heterogeneity of element distributions recently has received increased attention in soil science due to its influence on soil functions and soil fertility. We investigated the micro-scale distribution of total P and different specific P binding forms in aggregates taken from a high-P clay-rich soil and a low-P sandy soil by combining advanced spectrometric and spectroscopic techniques to introduce new insights on P accessibility and availability in soils. Here we show that soil substrate and soil depth determine micro-scale P heterogeneity in soil aggregates. In P-rich areas of all investigated soil aggregates, P was predominantly co-located with aluminium and iron oxides and hydroxides, which are known to strongly adsorb P. Clay minerals were co-located with P only to a lesser extent. In the low-P topsoil aggregate, the majority of the P was bound organically. Aluminium and iron phosphate predominated in the quartz-rich low-P subsoil aggregate. Sorbed and mineral P phases determined P speciation in the high-P top- and subsoil, and apatite was only detected in the high-P subsoil aggregate. Our results indicate that micro-scale spatial and chemical heterogeneity of P influences P accessibility and bioavailability.

Highlights

  • To cite this version: Florian Werner, Carsten W

  • The unavailability is a result of P leaching[1], strong chemical bonds with other elements such as calcium (Ca), iron (Fe), or aluminium (Al), e.g. as P minerals and as P bound to Al and Fe oxides and hydroxides, as well as to organic matter through metal cations[3], and immobilization of P in organic residues and microbial biomass[4]

  • soil organic matter (SOM) was strongly co-located with P in the low-P topsoil (16–31%, Table 1)

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Summary

Introduction

To cite this version: Florian Werner, Carsten W. We investigated the micro-scale distribution of total P and different specific P binding forms in aggregates taken from a high-P clay-rich soil and a low-P sandy soil by combining advanced spectrometric and spectroscopic techniques to introduce new insights on P accessibility and availability in soils. We show that soil substrate and soil depth determine micro-scale P heterogeneity in soil aggregates. Our results indicate that micro-scale spatial and chemical heterogeneity of P influences P accessibility and bioavailability. A robust assessment of the chemical and structural accessibility of P requires studying bulk P speciation in a soil or soil horizon, and spatial and chemical P heterogeneity at the micro-scale. Established chemical fractionation techniques of bulk soil[12], and advanced techniques of P speciation, as e.g. solution 31 P nuclear magnetic resonance spectroscopy[13] are inappropriate, because they destroy the structure of soil aggregates

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