This is shown for plant PD173074 species composition, richness and the functional composition over 258 grassland plots (Moeslund et al. 2013). This is further supported by a study on grasshoppers: south-facing pastures maintained a greater Orthoptera diversity than north facing pastures (Weiss et al. 2013); The authors further highlight that abundance is positively

correlated with bare ground (and in consequence grazing might be better than mowing). Apart from habitat size, isolation and/or landscape structure (like topography, see above), habitat quality (of both the particular habitat and the surrounding habitats) strongly influences the occurrence of species, and thus the species composition and diversity, as first demonstrated for the butterfly find more LXH254 datasheet Coenonympha tullia (Dennis and Eales 1997). For example the composition of plant species in wet grasslands is strongly affected by various abiotic factors like

chemical parameters of the soil, climatic conditions and human impact (Zelnik and Čarni 2013). In a study on Arbuscular Mycorrhizal Fungi (AMF), effects of land use, host plant neighbourhood and spatial arrangement on the AMF composition was tested over 67 grassland plots spread across the three German Biodiversity Exploratories (Morris et al. 2013). The authors show that the diversity of AMF react similar sensitive at both, large- and small scales; for example, the ability of AMF to provide protection from pathogens declined under high land-use intensity (Morris et al. 2013). Temporal and spatial gradients The floristic composition of plant communities is strongly influenced by biogeographic history; this is shown for the Dinaric versus Central-European region, both representing different biogeographical realms

(Pipenbaher Aurora Kinase et al. 2013). The authors explain the relevance of biogeographic history for the observed strong differences in floristic and functional composition of dry grassland communities. However, the processes leading to rarity in these grasslands were similar for both areas. A second contribution studying a temporal gradient highlights the effects of recent habitat transformations during the past decades, from 1970 until today (Filz et al. 2013). The authors showed that species composition changed from the past to present towards a generalist-species dominated community, despite habitat management activities, and they explain this trend by external factors as eutrophication and climate change. The following two contributions study effects along spatial gradients. Albrecht and Haider (2013) analyse effects of urbanisation (one of the main reason for decreasing grassland habitats) along a spatio-temporal urbanisation gradient from traditionally managed to urban developments.