Integrative phylogenetic, phylogeographic and morphological characterisation of the Unio crassus species complex reveals cryptic diversity with important conservation implications.

The global decline of freshwater mussels and their crucial ecological services highlight the need to understand their phylogeny, phylogeography and patterns of genetic diversity to guide conservation efforts. Such knowledge is urgently needed for Unio crassus, a highly imperilled species originally widespread throughout Europe and southwest Asia. Recent studies have resurrected several species from synonymy based on mitochondrial data, revealing U. crassus to be a complex of cryptic species. To address long-standing taxonomic uncertainties hindering effective conservation, we integrate morphometric, phylogenetic, and phylogeographic analyses to examine species diversity within the U. crassus complex across its entire range. Phylogenetic analyses were performed using cytochrome c oxidase subunit I (815 specimens from 182 populations) and, for selected specimens, whole mitogenome sequences and Anchored Hybrid Enrichment (AHE) data on âˆ¼ 600 nuclear loci. Mito-nuclear discordance was detected, consistent with mitochondrial DNA gene flow between some species during the Pliocene and Pleistocene. Fossil-calibrated phylogenies based on AHE data support a Mediterranean origin for the U. crassus complex in the Early Miocene. The results of our integrative approach support 12 species in the group: the previously recognised Unio bruguierianus, Unio carneus, Unio crassus, Unio damascensis, Unio ionicus, Unio sesirmensis, and Unio tumidiformis, and the reinstatement of five nominal taxa: Unio desectusstat. rev., Unio gontieriistat. rev., Unio mardinensisstat. rev., Unio nanusstat. rev., and Unio vicariusstat. rev. Morphometric analyses of shell contours reveal important morphospace overlaps among these species, highlighting cryptic, but geographically structured, diversity. The distribution, taxonomy, phylogeography, and conservation of each species are succinctly described.

Resident and Anadromous Forms of Arctic Charr (Salvelinus alpinus) from North-East Europe: An Example of High Ecological Variability without Speciation.

Samples from 11 populations of the Arctic char of the North-European part of Russia belonging to the anadromous and resident forms and two samples from Lake Sobach'e (Taimyr) were studied. The nucleotide sequence of the mitochondrial COI gene was determined in 60 individuals. In the majority of populations, the same COI haplotype was found. In some populations of the resident chars, haplotypes differing from the widespread haplotype in a single nucleotide substitution were found. The obtained genetic data give no reason to distinguish the resident form of the Arctic char from lakes of Karelia and the Kola Peninsula as an independent species, Salvelinus lepechini. The adaptation of the Arctic char to the unstable environmental conditions is ensured primarily by its phenotypic plasticity.

[The current flow of migrants and its contribution to Rhopalocera lepidopteran (Lepidoptera, Rhopalocera) fauna on marine islands with young allochthonous biotas].

The concept that the mechanisms limiting immigration of new Lepidoptera species are analogous for islands with different ages and degrees of endemism of their biotas is discussed. Specific features of individual species play a key role in establishment of the fauna and population on small islands rather than competitive interactions between these species. It is most likely that the species stably coexisting on an island will display similar ecological characteristics and life cycles, which complies with the concepts of the neutral theory of biodiversity and biogeography.

[Mechanism of population density compensation in island bumblebee taxocenoses (Hymenoptera, Apidae, Bombus) and the notion of reserve compensatory species].

The notion of a dynamic compensatory system is discussed, characterized by the alternation of species occupying the leading position in bumblebee taxocenoses, while the total density of these pollinators in island ecosystems remains at similar levels. The functioning of the compensatory system is regulated by both abiotic factors (the weather and climate) and biotic factors (competition for trophic resources). The stability of the system is determined by the presence of reserve compensatory species capable of rapid population growth against the background of depressed abundance of other species under changing environmental conditions.

[Results of testing the comparative method: the curvature of the shell valve frontal section is inappropriate as a systematic character for the freshwater pearl mussel of the genus Margaritifera].

This paper continues a discussion on the number of pearl mussel species of the genus Margaritifera in northern Europe. A biometric study of 1711 pearl mussel Margaritifera margaritifera shells from 15 rivers in Russia and Latvia (basins of the White and Baltic seas) has been conducted. All the examined samples fall into two groups: the northern group (with the shells more flattened on average, f. margaritifera) and the southern one (with more convex shells, f. elongata); the boundary between these groups is at 63 degrees N. Analysis of intrapopulation variation has shown that the samples contain individuals that correspond to f. margaritifera, f. elongata, and f. borealis. However, any hiatus between these forms is absent in all the samples, and individuals belonging to two intermediate forms are rather frequent. The hypothesis on the species specificity of the shell valve frontal section has not been confirmed based on examination of large shell samples. The pearl mussels inhabiting rivers of Northern Europe belong to a single species, M. margaritifera.

[Does freshwater pearl mussel (Margaritifera margaritifera) change life-history of Atlantic salmon (Salmo salar)?].

The critical analysis of the literature data shows that infection of freshwater pearl mussel glochidia does not influence the duration of freshwater period of the Atlantic salmon's life, as well as on all life cycle duration of this fish. Such infection does not influence health of Atlantic salmon or worsens slightly. There are no experimental data about symbiosis between pearl mussel and salmonid fishes.

[Freshwater Pearl mussels of the genus Margaritifera (Mollusca: Bivalvia) described as M. elongata (Lamarck, 1819) and M. borealis (Westerlund, 1871) should be classified with M. margaritifera (Linnaeus, 1758)].

The shells of Pearl mussels from the basins of the Solza, Keret', and Umba rivers flowing into the White Sea have been measured to determine the ratio of shell convexity to its maximum height. This ratio is the main character that, according to Bogatov et al. (2003), allows one to distinguish between three species of the genus Margaritifera: M. margaritifera, M. elongata, and M. borealis. It has been found that the above ratio gradually increases as the shell grows. Therefore, this character is unsuitable for species diagnosis, the more so that no hiatus in it between the three forms of pearl mussels has been revealed in any of the samples studied. On this basis, it may be concluded that Northern Europe, including Russia, is inhabited by only one species of pearl mussels, M. margaritifera.

[Dispersal routes and species identification of freshwater animals in Northern Europe: a review of molecular evidence].

According to genetic data, North European freshwater areas were colonized from refugia along the eastern Atlantic coast, in southern and eastern areas of Baltic Sea, in Siberia, North America, and areas of the Caspian and Black seas. Probably, a refugium also existed in Southern Norway. Colonization from the sea also took place. The taxonomic position of some forms, such as members of the complex groups of Arctic chars and coregonids, was refined in the course of combined studies including morphological analysis and molecular markers.

[Patterns of formation of island fauna of Rhopalocera (Lepidoptera, Diurna) at the northern forest boundary in the region of Pleistocene continental glaciation (by the example of White Sea islands)].

Patterns of formation of island Rhopalocera fauna at the northern forest boundary in the region of Valdai inland ice were analyzed by the example of White Sea islands. The ecotone effect, typical for northernmost taiga and forest-tundra and introducing the transitional Rhopalocera fauna in near-tundra forest between the boreal and hypoarctic zones, was not observed on the White Sea islands. Island isolation provided for the absence of some Arctic species, entering near-tundra forest from the North, in the island fauna. Island Rhopalocera faunas represent poor variants of the northern taiga fauna lacking some polyzonal and temperate species and having a reduced set of Arctic boreal species.