Three new papers from the lab have
been accepted during the last weeks. They will be published online early during
the next weeks/months, but here go the abstracts:
Ulrich, W., S. Soliveres, W. Kryszewski, F. T. Maestre & N. J. Gotelli. Matrix
models for quantifying competitive intransitivity from species abundance data. Oikos
In a network of competing species, a competitive
intransitivity occurs when the ranking of competitive abilities does not follow
a linear hierarchy (A>B>C but C>A). A variety of mathematical models
suggests that intransitive networks can prevent or slow down competitive exclusion
and maintain biodiversity by enhancing species coexistence. However, it has
been difficult to assess empirically the relative importance of intransitive
competition because a large number of pairwise species competition experiments are
needed to construct a competition matrix that is used to parameterize existing
models. Here we introduce a statistical framework for evaluating the
contribution of intransitivity to community structure using species abundance
matrices that are commonly generated from replicated sampling of species
assemblages. We provide metrics and analytical methods for using abundance matrices
to estimate species competition and patch transition matrices by using reverse-engineering
and a colonization-competition model. These matrices provide complementary
metrics to estimate the degree of intransitivity in the competition network of
the sampled communities. Benchmark tests
reveal that the proposed methods could successfully detect intransitive competition networks, even in the
absence of direct measures of pairwise competitive strength. To illustrate the approach,
we analyzed patterns of abundance and biomass of five species of necrophagous
Diptera and eight species of their hymenopteran parasitoids that co-occur in
beech forests in Germany. We found evidence for a strong competitive hierarchy
within communities of flies and parasitoids. However, for parasitoids, there
was a tendency towards increasing intransitivity in higher weight classes,
which represented larger resource patches. These tests provide novel methods for
empirically estimating the degree of intransitivity in competitive
networks from observational datasets. They can be applied to experimental
measures of pairwise species interactions, as well as to spatio-temporal samples
of assemblages in homogenous environments or environmental gradients.
Escudero,
A., S. Palacio, F. T. Maestre &
A. Luzuriaga. 2014. Plant life on gypsum: a review of its multiple
facets. Biological Reviews
The adaptation of plants to particular soil types has long intrigued
biologists. Gypsum soils occupy large areas in many regions of the world and
host a striking biological diversity, but their vegetation has been much less
studied than that developing over serpentine or saline soils. Herein, we review
all aspects of plant life on gypsum ecosystems, discuss the main processes
driving their structure and functioning, and highlight the main conservation
threats that they face. Plant communities in gypsum habitats typically show
distinctive bands at very small spatial scales, which are mainly determined by
topography. Plants living on gypsum soils can be classified into three
categories: (i) wide gypsophiles are specialists that can penetrate the
physical soil crust during early life stages and have physiological adjustments
to cope with the chemical limitations imposed by gypsum soils; (ii) narrow
gypsophiles are refugee plants which successfully deal with the physical soil
crust and can tolerate these chemical limitations but do not show specific
adaptations for this type of soils; and (iii) gypsovags are non-specialist
gypsum plants that can only thrive in gypsum soils when the physical crust is
absent or reduced. Their ability to survive in gypsum soils may also be
mediated by below-ground interactions with soil microorganisms. Gypsophiles and
gypsovags show efficient germination at low temperatures, seed and fruit
heteromorphism within and among populations, and variation in seed dormancy
among plants and populations. In gypsum ecosystems, spatio-temporal changes in
the composition and structure of aboveground vegetation are closely related to
those of the soil seed bank. Biological soil crusts (BSCs) dominated by
cyanobacteria, lichens and mosses are conspicuous in gypsum environments
worldwide, and are important drivers of ecosystem processes such as carbon and
nitrogen cycling, water infiltration and run-off and soil stability. These
organisms are also important determinants of the structure of annual plant
communities living on gypsum soils. The short-distance seed dispersal of
gypsophiles is responsible for the high number of very narrow endemisms
typically found in gypsum outcrops, and suggests that these species are
evolutionarily old taxa due to the time they need to colonize isolated gypsum
outcrops by chance. Climate change and habitat fragmentation negatively affect
both plants and BSCs in gypsum habitats, and are among the major threats to
these ecosystems. Gypsum habitats and specialists offer the chance to advance
our knowledge on restrictive soils, and are ideal models not only to test
important evolutionary questions such as tolerance to low Ca/Mg proportions in
soils, but also to improve the theoretical framework of community ecology and
ecosystem functioning.
Guerrero,
C., B. Stenberg, J. Wetterlind, R. A. Viscarra Rossel, A. M. Mouazen, R.
Zornoza, F. T. Maestre, J. D.
Ruiz-Sinoga & B. Kuang. 2014. Assessment
of soil organic carbon at local scale with spiked NIR calibrations: effects of selection
and extra-weight of the spiking subset. European Journal of Soil Science
Spiking is an interesting approach to improve the accuracy of regional
or national spectroscopic calibrations when they are used to predict at local.
For doing this, a small subset of local samples (spiking subset; SS) is added
to recalibrate the regional or national calibration. If the SS is small in
comparison with the size of the initial calibration (IC) set, then the
information added with this SS could have a little noticeable effect, and the
improvement in the calibration model is also small. For these reasons, we
hypothesised that the accuracy of the spiked calibrations can be improved when
the statistical relevance of the SS is extra-weighted (EW). Moreover, we also
hypothesised that the selection of the SS, and also the size of the IC set are relevant
and can affect the accuracy of the recalibrated models. With the aim to test
these hypotheses, we have evaluated thirteen different strategies, without and
with EW, to select the best SS to spike three ICs of different sizes. These
calibrations were used to predict the soil organic carbon (SOC) in samples from
four independent target sites. The results confirmed that spiking improves the
prediction accuracy of the ICs. The accuracy was significantly improved when
the SS was EW. This result is very interesting because EW is a simple, fast and
inexpensive task. As expected, we observed differences in accuracy depending on
the SS used. The best results were obtained with the SS containing local
samples evenly distributed in the spectral space, regardless the
characteristics of the ICs. The best results were obtained using the small- and
medium-sized ICs, suggesting that incipient spectral libraries could be useful
if the SS is properly selected and EW. Overall, our results indicate that the
efforts needed for the use NIR spectroscopy for SOC assessment at local scale
can be minimized by using EW, which is highly recommended when calibrations are
spiked.
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