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@ARTICLE{Jiang:276177,
author = {Jiang, Xiaoqian and Bol, R. and Willbold, S. and Vereecken,
H. and Klumpp, E.},
title = {{S}peciation and distribution of {P} associated with {F}e
and {A}l oxides in aggregate-sized fraction of an arable
soil},
journal = {Biogeosciences discussions},
volume = {12},
number = {13},
issn = {1810-6285},
address = {Katlenburg-Lindau [u.a.]},
publisher = {Copernicus},
reportid = {FZJ-2015-06644},
pages = {9879 - 9903},
year = {2015},
abstract = {To maximize crop productivity fertilizer P is generally
applied to arable soils, a significant proportion of which
becomes stabilized by mineral components and in part
subsequently becomes unavailable to plants. However, little
is known about the relative contributions of the different
organic and inorganic P bound to Fe/Al oxides in the smaller
soil particles. The alkaline (NaOH-Na2EDTA) extraction with
solution 31P-nuclear magnetic resonance (31P-NMR)
spectroscopy is considered as a reliable method for
extracting and quantifying organic P and (some) inorganic P.
However, any so-called residual P after the alkaline
extraction has remained unidentified. Therefore, in the
present study, the amorphous (a) and crystalline (c) Fe/Al
oxide minerals and related P in soil aggregate-sized
fractions (> 20, 2–20, 0.45–2 and < 0.45 μm) were
specifically extracted by oxalate (a-Fe/Al oxides) and
dithionite (DCB, both a- and c-Fe/Al oxides). These soil
aggregate-sized fractions with and without the oxalate and
DCB pre-treatments were then sequentially extracted by
alkaline extraction prior to solution 31P-NMR spectroscopy.
This was done to quantify the various chemical P forms which
were associated with a- and c-Fe/Al oxides both in alkaline
extraction and in the residual P of different soil
aggregate-sized fractions.The results showed that overall P
contents increased with decreasing size of the soil
aggregate-sized fractions. However, the relative
distribution and speciation of varying P forms were found to
be independent of soil aggregate-size. The majority of
alkaline extractable P was in the a-Fe/Al oxide fraction
(42–47 $\%$ of total P), most of which was orthophosphate
(36–41 $\%$ of total P). Furthermore, still significant
amounts of particularly monoester P were bound to the
oxides. Intriguingly, however, Fe/Al oxides were not the
main bonding sites for pyrophosphate. Residual P contained
similar amounts of total P associated with both a- (10–13
$\%$ of total P) and c-Fe oxides (10–12 $\%$ of total P)
in various aggregate-sized fractions, suggesting that it was
likely occluded within the a- and c-Fe oxides in soil. This
implies that with the dissolution of Fe oxides, these P may
be released and thus available for plants and microbial
communities.},
cin = {IBG-3 / ZEA-3},
ddc = {570},
cid = {I:(DE-Juel1)IBG-3-20101118 / I:(DE-Juel1)ZEA-3-20090406},
pnm = {255 - Terrestrial Systems: From Observation to Prediction
(POF3-255)},
pid = {G:(DE-HGF)POF3-255},
typ = {PUB:(DE-HGF)16},
doi = {10.5194/bgd-12-9879-2015},
url = {https://juser.fz-juelich.de/record/276177},
}