Forschungszentrum Landschaftsentwicklung und Bergbaulandschaften (FZLB)
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An interactive survey panel regarding the effects of mice (Microtus spec.) on a young ecosystem
(2015)
It is widely acknowledged that increasing complexity is a key attribute of ecosystem genesis. This is particularly true for primary succession on homogeneous substrates. However, a mechanistic understanding of spatial colonisation and pattern formation during primary succession has not been achieved yet. Thus, we studied this topic for 7 years within an experimental catchment (6 ha) established in the post-mining landscape of eastern Germany. Equidistant permanent plots (120 plots à 25m²) allowed for autocorrelation analyses, and thus tracing the spatial development of species cover performance. For each species tested, the “cover balance” first increased due to colonization, while decreasing in the course of succession. Drawing a benefit from these temporal trends, we suggested cover balance levels revealed by autocorrelation analyses to best indicate well-defined phases in primary succession at spatial entities. Hence, with the help of this spatial approach, terrestrial succession can be understood now much better at the most general level of the hierarchy provided by Pickett et al. (1987). In accordance with these authors, at subordinated levels of the causal hierarchy differential species performance might get collectively explained by contributing processes or conditions, such as ecophysiological traits, life history strategies, competition and allelopathy of the occurring plant species. Further research is needed to understand their relative contributions to the pattern formation.
We hypothesized that at the very beginning of terrestrial ecosystem development, airborne testate amoebae play a pivotal role in facilitating organismic colonization and related soil processes. We, therefore, analyzed size and quantity of airborne testate amoebae and immigration and colonization success of airborne testate amoebae on a new land surface (experimental site “Chicken Creek”, artificial post-mining water catchment). Within an altogether 91-day exposure of 70 adhesive traps, 12 species of testate amoebae were identified to be of airborne origin. Phryganella acropodia (51% of all individuals found, diameter about 35–45 μm) and Centropyxis sphagnicola (23% of all individuals found, longest axis about 55–68 μm), occurred most frequently in the adhesive traps. We extrapolated an aerial amoeba deposition of 61 individuals d−1 m−2 (living and dead individuals combined). Although it would be necessary to have a longer sequence (some additional years), our analysis of the “target substrate” of aerial immigration (catchment site) may point to a shift from a stochastic (variable) beginning of community assembly to a more deterministic (stable) course. This shift was assigned to an age of seven years of initial soil development. Although experienced specialists are necessary to conduct these time-consuming studies, the presented data suggest that terrestrial amoebae are suitable indicators for initial ecosystem development and utilization.
Monitoring of ecosystem patterns and processes in an artificial catchment in Lusatia, Germany
(2009)
During early plant succession, the phylogenetic structure of a community changes in response to important environmental filters and emerging species interactions. We traced the development of temperate-zone plant communities during the first 7 years of primary succession on catchment soils to explore patterns of initial species assembly. We found pronounced small-scale differences in the phylogenetic composition of neighbouring plant assemblages and a large-scale trend towards phylogenetic evenness. This small-scale variability appears to be mediated by soil properties,
particularly carbonate content. Therefore, abiotic environmental conditions might counteract or even supersede the effects of interspecific competition among closely related species, which are usually predicted to exhibit patterns of phylogenetic evenness. We conclude that theories
on phylogenetic community composition need to incorporate effects of small-scale variability of environmental factors.