% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Temperton:21191,
author = {Temperton, V.M. and Märtin, L.L.A. and Röder, D. and
Lücke, A. and Kiehl, K.},
title = {{E}ffects of four different restoration treatments on the
natural abundance of 15{N} stable isotopes in plants},
journal = {Frontiers in plant science: FPLS},
volume = {3},
issn = {1664-462X},
address = {Lausanne},
publisher = {Frontiers Media},
reportid = {PreJuSER-21191},
pages = {70},
year = {2012},
note = {Record converted from VDB: 12.11.2012},
abstract = {δ(15)N signals in plant and soil material integrate over a
number of biogeochemical processes related to nitrogen (N)
and therefore provide information on net effects of multiple
processes on N dynamics. In general little is known in many
grassland restoration projects on soil-plant N dynamics in
relation to the restoration treatments. In particular,
δ(15)N signals may be a useful tool to assess whether
abiotic restoration treatments have produced the desired
result. In this study we used the range of abiotic and
biotic conditions provided by a restoration experiment to
assess to whether the restoration treatments and/or plant
functional identity and legume neighborhood affected plant
δ(15)N signals. The restoration treatments consisted of hay
transfer and topsoil removal, thus representing increasing
restoration effort, from no restoration measures, through
biotic manipulation to major abiotic manipulation. We
measured δ(15)N and $\%N$ in six different plant species
(two non-legumes and four legumes) across the restoration
treatments. We found that restoration treatments were
clearly reflected in δ(15)N of the non-legume species, with
very depleted δ(15)N associated with low soil N, and our
results suggest this may be linked to uptake of ammonium
(rather than nitrate). The two non-legume species differed
considerably in their δ(15)N signals, which may be related
to the two species forming different kinds of mycorrhizal
symbioses. Plant δ(15)N signals could clearly separate
legumes from non-legumes, but our results did not allow for
an assessment of legume neighborhood effects on non-legume
δ(15)N signals. We discuss our results in the light of what
the δ(15)N signals may be telling us about plant-soil N
dynamics and their potential value as an indicator for N
dynamics in restoration.},
cin = {IBG-3 / IBG-2},
ddc = {570},
cid = {I:(DE-Juel1)IBG-3-20101118 / I:(DE-Juel1)IBG-2-20101118},
pnm = {Terrestrische Umwelt},
pid = {G:(DE-Juel1)FUEK407},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22645597},
pmc = {pmc:PMC3355755},
UT = {WOS:000208837900071},
doi = {10.3389/fpls.2012.00070},
url = {https://juser.fz-juelich.de/record/21191},
}