Meaningful ecological studies on insect communities require sampling protocols that take into consideration temporal fluctuations in abundance and species composition. Bees with their specific requirements for nutrition and nesting are good indicators of landscape structure and overall biodiversity, provided the ecological and seasonal patterns they show are taken into consideration. The present two year study traced the ecological and seasonal patterns on 2 km2 of a southern slope in the Swiss Alps, ranging from 1150 to 1550 m above sea level. The study area consisted mainly of grassland under different regimes, mostly hay meadows and pastures. By direct netting at five monthly intervals in each year a total of 247 bee species were recorded. This comprehensive sampling scheme identified one of the most diverse bee faunas in Central and Northern Europe, consisting of a statistically estimated 280 species. Most species were rare with 14.6% represented by a single individual. Ecological analysis of the bee community showed that the primitively eusocial species were over represented among the abundant species and the parasitic species among the rarest.
Both abundance and species richness were subject to marked seasonal variations. A substantial turnover in species composition as well as changes in ecological patterns were observed. More than 25% of all species were recorded in only one of the two years, in particular many of the parasitic species. Singletons accounted for a higher proportion when individual years rather than the pooled data were analysed. All these findings underline the importance of season-long sampling and sampling over more than one year if bees are to be used as indicators in ecological and studies on bee communities.
The intermediate disturbance hypothesis predicts that species diversity in biotic communities should peak at intermediate levels of disturbance. The vegetation of eight calcareous screes in the Northern Calcareous Alps, Austria was studied to test this hypothesis. Data on total vegetation cover and on cover of individual species were obtained from 0.25 m2 , 0.5 m2 , and 1.0 m2 plots. An index [100 – vegetation cover (%)] was used as a surrogate for direct quantification of disturbance (movement of stones and destruction of biomass). Its suitability was substantiated by the observation of position changes of marked stones after two years. In agreement with the intermediate disturbance hypothesis, significant unimodal responses of both species richness and species diversity to disturbance were found using plots of all three sizes. However, the maxima of species richness- and species diversity-disturbance curves were shifted towards higher vegetation cover (= lower disturbance) with increasing mean diameters of the scree-building stones. This shift can be interpreted either as a synergistic effect of disturbance frequency combined with disturbance intensity/extent, or as a result of an increase in spatial heterogeneity promoting species coexistence in successionally more advanced patches of vegetation.