For conservation of forest biodiversity, dead wood in the form of logs, snags, or cut high stumps is sometimes left or created when forests are harvested. In Scandinavia, such dead wood usually comes from conifers. For forests in temperate regions, few studies have analysed composition and species richness of beetles using dead wood of oaks ( Quercus spp). In this study in southern Sweden, I examined the occurrence of saproxylic beetles trapped at lying (logs) and standing (snags) dead wood of European oaks ( Quercus robur L. and Quercus petraea (Mattuschka) Liebl.) in 13 oak-rich mixed forests of relatively high conservation value. The assemblage of beetles differed strikingly between the lying and standing dead wood. Traps on lying dead wood, compared to traps on standing dead wood, had more fungivores and fewer primary and secondary wood boring species. Of 94 species tested for individual substrate preferences, 48 showed prevalence for different trap/substrate types. Absolute species richness was significantly higher on logs than snags, but a smaller proportion of the snag substrate or snag beetles may have been sampled. For red-listed beetles, no differences in their species richness were detected among substrates. These results suggest that logs of dead oaks are valuable and that both snags and logs of oak should be retained and, if needed, created in forestry, such that they are continuously available in stands.
Aim To investigate the relative role of local versus landscape factors for local species diversity of snails and slugs in conservation forests. In landscapes with small, isolated patches of semi‐natural habitats, many species that require large habitat areas have disappeared or are threatened. We asked whether small sedentary taxa that depend on local conditions, such as molluscs, are affected if total habitat area decreases in the landscape.
Location Temperate broadleaved and oak‐rich forest in southern Sweden.
Methods We sampled molluscs in 25 small conservation forests that are well‐spaced out over a large region. In each forest, sampling was conducted in two plots, each of 1 ha, separated by about 25–100 m. Factors potentially influencing local diversity of molluscs were measured in the plots and in the surrounding landscape at different scales (in space and time) and were analysed by stepwise multiple regression and ordination (PCA and NMS).
Results We recorded 53 species, and mean species richness per forest (plots pooled) was 22.6. The pH of the plant litter predicted both species richness and composition; other local (plot) factors of lower importance were canopy openness, stony ground and tree species. The area of conservation forest (woodland key habitat) within 10 km of plots was positively associated with species richness, and was also related to species composition. Openness of the landscape (agriculture) was a negative factor, but historical plot openness (1938–59) seemed to be unimportant. In addition, climate/topography (temperature and altitude) also predicted species composition of the sites.
Main conclusions We rejected the hypothesis that microhabitat factors alone, or mainly, determine local species richness and composition of land molluscs. These representatives of small, sedentary organisms seem to be substantially influenced by the surrounding landscape, which should be considered in conservation work and in plans for the protection of forest biodiversity.
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