To the hoverflies fauna (Diptera: Syrphidae) of the high mountains of Eastern Sayan in Siberia

A list of 101 species of hoverflies recorded from three high altitudinal belts in the Eastern Sayan mountain region is given. Most species belong to the subfamilies Syrphinae (60 species) and Eristalinae (38 species), while Pipizinae and Microdontinae are presented by two and one species, respectively. Totally, 96 species were found in the forest zone, 37 species were found in the mountain tundra and only Platycheirus chilosia has been caught in the golsty belt. New synonymy is established: Melangyna arctica (Zetterstedt, 1838) = Melangyna soszynskii Mielczarek, 2013 syn. n., = Melangyna tsherepanovi (Violovitsh, 1965) syn. n.

The vegetation cover of the «Aryskannyg» cluster of the «Ubsunurskaya Kotlovina» Reserve (Ubsunur hollow) (the southern slopes of the East Tannu-Ola Mountain Range, Republic of Tyva)

This paper studies the vegetation cover organization of the Aryskannyg cluster of the state natural biosphere reserve Ubsunurskaya Kotlovina. In the course of the work 2 ecological and phytocoenotic profiles were laid and 2 large-scale mapping was carried out. The steppe type of vegetation is mainly represented by different variants of real turf-and-slag steppes: shrubby, petrophytic and dry. The original steppe communities are the resurrection ( Selaginella sanguinolenta ) and eastern feather grass coenoses ( Stipa orientalis ). An independent high-altitude belt forms mountain expositional forest-steppes. The forest component consists of grass and rhytidium larch forests, and the daurian rhododendron occupies an active position in the undergrowth. The steppe component consists of thickened mixed-grass-stop-grass meadow, as well as mixed-grass-fine-grained-slag petrophytic steppes. The mountain-taiga belt is represented by communities of larch and cedar formations. The high-altitude belt is dominated by yernik ( Betula rotundifolia ) and dryad ( Dryas oxyodontha ) mountain-tundra communities. It is revealed that the territory has a complex vegetation cover, which was formed in the conditions of mountain relief and sharply continental climate, the diversity of plant communities (from dry-steppe to mountain-tundra) is due to the length of the cluster territory in three high-altitude zones and the complex influence of latitudinal and local abiotic factors. The leading factors in the distribution of vegetation are the exposure of the slopes and the absolute height of the terrain.

The origin of the mountain (goltzy) deserts of the European Arctic: A review of theories .

The main theories of origin of the European Arctic tundra and subarctic mountain(goltzy)deserts are reviewed, in application to the Kola Peninsula. The theory of «tabula rasa» stated that all plants died during glaciation, and then immigrated fromtheCentral Europe, Siberia, and British Isles. According to another theory, during several Pleistocene glaciations, plants survived in ice-free refugia. Modern bota-ny point of views supports post-glacial migration of species and rather «tabula rasa»theory. The border of the timberline moving up inthe Holocene thermal optimum did not affect the subarctic mountain de-serts, unlike the tundra zone. Based on this, the evolution of the high mountain deserts vegetation probably meant the establishment of groups of species that differ from modern communities of the lower disposed tundra zone. Many types of mountain tundra vegetation, apparently, came from the mountains of North-East Azia; however, many species have been originated from the forest communi-ties. The subarctic mountain deserts have apparently not changed since the retreat of the glacier.

The first report on the oribatid mites (Acari: Oribatida) in tundra of the Chunatundra Mountains on the Kola Peninsula, Russia

The aim of this research was to obtain initial data on the fauna and abundance of the oribatid mites from the main types of the mountain tundra habitats of the Chunatundra Mountains. Four plots, including two lichen tundra plots, one dwarf shrub tundra plot and one sphagnum bog in the belt of mountain tundra were investigated. Multidimensional scaling and discriminant function analysis were used to identify trends in the fauna and abundance of oribatid species through the explored plots. A total of 70 species and one subspecies from 37 genera and 24 families were found during the course of this investigation. Nine species, one subspecies, one genus and one family of oribatid mites have been added to the fauna of the Kola Peninsula. The families Brachychthoniidae, Oppiidae and Suctobelbidae are the most diverse in the discovered local fauna. According to literature data, the first two families are characteristic of the low tundra communities, the third family is more common for the boreal zone. The discovered oribatid fauna is similar to the fauna of other tundra sites of the Kola Peninsula studied previously and is significantly different to the local oribatid mite faunae of the Scandinavian Peninsula. The abundance of the adult oribatid mites reached 39 080 ind./m2 in the lichen tundra and 56 200 ind./m2 in the dwarf shrub tundra. The minimum abundance of oribatid mites, 18 640 ind./m2 was found in the sphagnum bog. Differences in the oribatid mite complexes of lichen tundra, dwarf shrub tundra and the sphagnum bog were found. The species Carabodes labyrinthicus, Nothrus borussicus, Sellnickochthonius immaculatus, Mycobates sarekensis, and Tectocepheus velatus were associated with the lichen tundra habitats. Nanhermannia sellnicki, Chamobates borealis and a few species of Oppiella and Suctobelbella were associated with the dwarf shrub tundra. Mucronothrus nasalis, Limnozetes ciliatus, Platynothrus peltifer, Trimalaconothrus foveolatus, Limnozetes cf. rugosus, and Trimalaconothrus maior are most characteristic of the sphagnum bog. The family Suctobelbidae was represented by a large number of species, while the families Ceratozetidae and Camisiidae were much less diverse. The low diversity of Ceratozetidae, a high diversity of Suctobelbidae and relatively high abundance of oribatid mites in the explored tundra habitats may be explained by an ambivalent nature of the oribatid community, which combines boreal and arctic features due to marine climate. Also, this result may be a feature of a local mountain tundra which is surrounded by the underlying belts of the mountain forests that are a source of the increasingly diversity of species.