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The African species Cheiracanthium furculatum Karsch, 1879 was recognised as being introduced to Germany and is re-described and illustrated in the present study. C. tenuipes Roewer, 1961 is recognised as a junior synonym of C. africanum Lessert, 1921 (new synonymy); both subspecies of C. strasseni Strand, 1915, namely C. strasseni strasseni Strand, 1915 and C. strasseni aharonii Strand, 1915, are recognised as junior synonyms of C. mildei L. Koch, 1864 (new synonymies). Photographic images of the copulatory organs of the types of C. cretense Roewer, 1928, recently synonymised with C. mildei, are provided and discussed in the course of intraspecific variation in C. mildei. The female holotype of C. rehobothense Strand, 1915 is re-described and illustrated. Relations of C. rehobothense to other Cheiracanthium species are discussed.
Sauron rayi (Simon, 1881) is recorded in Austria for the first time. Male and female specimens of this rare European spider were found in two “Austrian pine forests” in Lower Austria. Data on distribution, habitat, phenology and Red List status from the Austrian localities and from published records in other countries are presented.
The knowledge of phenotypic variation in the European range of the highly allergenic Ambrosia artemisiifolia L. (common ragweed) is not entirely complete, even though it is an invasive species of utmost concern. We hypothesized the prevalence of phenotypic differentiations between common ragweed populations in the introduced range, and we assumed that those differentiations were related to environmental conditions at the points of origin. Using a common garden experiment, we investigated biomass allocation, growth rates, and flowering phenology of 38 European common ragweed populations originating from a major geographical gradient. We observed considerable phenotypic variation in growth parameters and flowering phenology, e.g. mean aboveground biomass varied from 23.3 to 47.3 g between the populations. We were able to relate most measured traits with environmental parameters prevailing at the points of origin. For example, early growth of ruderal populations was highly correlated with temperature and precipitation at the point of origin. Late growth and flowering phenology were highly correlated with latitude, i.e. individuals from northern populations grew smaller and flowered and dispersed their pollen and seeds up to 5 weeks earlier than individuals from southern populations. We also found a longitudinal gradient in flowering phenology which has not yet been described. The existence of such a high variability in the introduced range may facilitate further range expansion. We suggest that the correlation with environmental variables rests upon genetic variation possibly due to adaptations to the respective environment. To clarify if such adaptation results from multiple events of introduction or as evolutionary response after introduction, genetic investigations are needed.