Abstract. Geographic variation can lead to the evolution of different local varieties within a given species, therefore influencing its distribution and genetic structure. We investigated the contribution of plasticity and local adaptation to the performance of a common aquatic plant (Potamogeton pectinatus) in contrasting climates, using reciprocal transplants at three experimental sites across a latitudinal cline in Europe. Plants from 54 genets, originally collected from 14 populations situated within four climatic regions (subarctic, cold temperate, mild temperate, and mediterranean) were grown in three different localities within three of these regions (cold temperate, Norway; mild temperate, The Netherlands; mediterranean, Spain). Tuber production was highest for the mild-temperate genets, irrespective of locality where the genets were grown. Selection coefficients indicated that populations at the European center of the species distribution perform better than all other populations, at all sites. However, marginal populations showed changes in life-history traits, such as compressed life cycles in the north and true perenniality in the south, that may allow them to perform better locally, at the limits of their distribution range. Our results thus suggest that local adaptation may overlap spatially with center-periphery gradients in performance caused by genetic factors (such as genetic drift and inbreeding in range-marginal populations).

Niche and neutral processes drive community assembly and metacommunity dynamics, but their relative importance might vary with the spatial scale. The contribution of niche processes is generally expected to increase with increasing spatial extent at a higher rate than that of neutral processes. However, the extent to what community composition is limited by dispersal (usually considered a neutral process) over increasing spatial scales might depend on the dispersal capacity of composing species. To investigate the mechanisms underlying the distribution and diversity of species known to have great powers of dispersal (hundreds of kilometres), we analysed the relative importance of niche processes and dispersal limitation in determining beta‐diversity patterns of aquatic plants and cladocerans over regional (up to 300 km) and continental (up to 3300 km) scales. Both taxonomic groups were surveyed in five different European regions and presented extremely high levels of beta‐diversity, both within and among regions. High beta‐diversity was primarily explained by species replacement (turnover) rather than differences in species richness (i.e. nestedness). Abiotic and biotic variables were the main drivers of community composition. Within some regions, small‐scale connectivity and the spatial configuration of sampled communities explained a significant, though smaller, fraction of compositional variation, particularly for aquatic plants. At continental scale (among regions), a significant fraction of compositional variation was explained by a combination of spatial effects (exclusive contribution of regions) and regionally‐structured environmental variables. Our results suggest that, although dispersal limitation might affect species composition in some regions, aquatic plant and cladoceran communities are not generally limited by dispersal at the regional scale (up to 300 km). Species sorting mediated by environmental variation might explain the high species turnover of aquatic plants and cladocerans at regional scale, while biogeographic processes enhanced by dispersal limitation among regions might determine the composition of regional biotas.

GORNALL, R. J., 1987. An outline of a revised classification of Saxifraga. A revised classification of Saxifraga is presented in which 15 sections, 19 subsections and 34 series are recognized. A total of 394 names are accounted for, including the following new taxa, combinations and names: series Hirculoideae (Engler & Irmscher) Gornall, stat. nov.; series Lychnitidae (Engler & Irmscher) Gornall, stat. nov.; series Nulanles (Engler & Irmscher) Gornall, stat. nov.; series Cinctae (H. Sm.) Gornall, stat. nov.; series Gemmiparae (Engler & Irmscher) Gornall, stat. nov.; series Spinulosae (C. B. Clarke) Gornall, stat. nov.; subsection Rosulares Gornall, nom. nov.; subsection Serpyllifoliae Gornall, subscct. nov.; subsection Hemisphaericae (Engler & Irmscher) Gornall, stat. nov.; section Merkianae (Engler & Irmscher) Gornall, stat. nov.; subsection Stellares (Engler & Irmscher) Gornall, stat. nov.; series Birostres Gornall, ser. nov.; series Melanocentrae (Engler & Irmscher) Gornall, stat. nov.; series Astasianlhes (Sternberg) Gornall, stat. nov.; subsection Micranthes (Haworth) Gornall, stat. nov.; series Aulaxis (Haworth) Gornall, stat. nov.; series Dermasea (Haworth) Gornall, stat. nov.; series Micranthes (Haworth) Gornall, stat. nov.; scries Aretioideae (Engler & Irmscher) Gornall, stat. nov.; series Juniperifoliae (Engler & Irmscher) Gornall, stat. nov.; series Lilacinae Gornall, ser. nov.; series Marginatae (Engler & Irmscher) Gornall, stat. nov.; series Squarrosae (Engler & Irmscher) Gornall, stat. nov.; series Rigidae (Engler & Irmscher) Gornall, stat. nov.; subsection Engleria (Siindermann) Gornall, stat. nov; series Subsessiliflorae Gornall, ser. nov.; series Oppositiofoliae (Hayek) Gornall, stat. nov.; series Tetrameridium (Engler) Gornall, stat. nov.; subsection Mutatae (Engler & Irmscher) Gornall, stat. nov.; subsection Florulentae (Engler & Irmscher) Gornall, stat. nov.; section Odontophyllae Gornall, sect, nov.; series Biternatae (Engler & Irmscher) Gornall, stat. nov.; subsection Triplinervium (Gaudin) Gornall, stat. nov.; series Arachnoideae (Engler & Irmscher) Gornall, stat. nov.; subsection Tridactylites (Haworth) Gornall, stat. nov.

No abstract

Nearly half of the species in the large genus Saxifraga belong to Saxifraga sect. Ciliatae, a largely Sino‐Himalayan taxon. We report here that evidence from chloroplast DNA sequences (psbA‐trnH, trnL‐F) and from nuclear sequences (ITS) indicates that this section is monophyletic and composed of at least three main lineages, corresponding to (1) a clade made up of species from S. subsect. Gemmiparae, subsect. Cinerascentes, subsect. Flagellares and subsect. Hemisphaericae, in which the last three subsections are nested in the first; (2) a clade of species belonging to S. subsect. Rosulares (including S. subsect. Serpyllifoliae); and (3) a clade of species belonging to S. subsect. Hirculoideae. Species relationships in S. subsect. Rosulares and subsect. Hirculoideae are not well resolved. A molecular clock analysis indicates that the diversification of S. sect. Ciliatae into its three lineages dates from ca. 9.48 Ma, coinciding with orogenic events associated with one of the most important phases of uplift of the Qinghai‐Tibet Plateau. Extensive diversifications within S. subsect. Rosulares and subsect. Hirculoideae have been more recent (ca. 4.51 Ma and 2.12 Ma, respectively), again correlated with Qinghai‐Tibet Plateau uplift events and, in the case of S. subsect. Hirculoideae, have occurred at a rate comparable to that seen in the radiation of Hawaiian fruit flies.