The Dzungarian Gobi (DzG), one of 16 phytogeographical regions in the country, is located in the southwestern part of Khovd province in western Mongolia. It comprises some of Mongolia’s largest reserves, namely the Great Gobi B Strictly Protected Area and the National Park Bulgan gol-Ikh Ongog. We conducted a comprehensive survey of the area’s floristic diversity between 2009 and 2019 by collecting vascular plants from different vegetation types in various seasons. In addition, we critically checked relevant published literature and material from the herbaria ALTB, GLM, GWF, HAL, KHU, LE, MW, NS, OSBU, UBA, and UBU to determine the occurrence of vascular plant species in the DzG region. Based on our collection data, a comprehensive checklist of DzG’s flora was compiled, representing 913 vascular plant taxa (including 34 subspecies and one variety) belonging to 329 genera and 70 families. Twenty-one taxa were newly found in the DzG region. We also investigated the conservation status of all species noted, and 19 endemic plants and 96 threatened species, including six critically endangered, 26 endangered, 57 vulnerable, and seven near threatened plants were recognized in this region. Eight rare species were newly assessed according to regional conservation status based on GeoCat and IUCN. The richest plant families found were Asteraceae (153 species), Fabaceae (77 species), Amaranthaceae (69 species), and Poaceae (68 species). Several uncertain endemic and non-endemic plants remain still discussion, such as Papaver baitagense and Rosa baitagensis; thus, further studies are needed on their taxonomic and conservation status. For each taxon, we provide its distribution in the region, elevation range, voucher number, and additional references. Finally, we analyzed species hotspots of DzG, based on three different plant species richness criteria: i. all recorded species, ii. endemic species, and iii. threatened species using our georeferenced records. The most diverse hotspot area in DzG is the Baitag Bogd Mountain area, which comprises the highest species number of all three richness criteria.

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www.ssbg.asu.ru/turczaninowia.php Summary. A new system of the family Woodsiaceae is proposed. A new genus Woodsiopsis is described and new combinations in the genera Physematium, Eriosoriopsis, and Woodsiopsis are validated. The systems of Woodsia and Eriosoriopsis are clarified and new intrageneric taxa in these genera are established. Резюме. Предложена новая система семейства Woodsiaceae. Описан новый род Woodsiopsis, обнародованы новые комбинации в родах Physematium, Eriosoriopsis и Woodsiopsis. Уточнены системы родов Woodsia и Eriosoriopsis, в которых описаны новые внутриродовые таксоны.

Constituting one of Earth’s major biomes, steppes are characterised by naturally treeless extra-tropical vegetation. The formation of the Eurasian steppe belt, the largest steppe region in the world, began in Central Asia during the Neogene. In the glacial stages of the Pleistocene, steppe displaced forest vegetation, which in turn recolonised the area during the warmer interglacial periods, thus affecting the distribution of plants adapted to these habitats. Krascheninnikovia ceratoides (Chenopodiaceae) is a plant characteristic of dry steppe and semi-desert formations. Earlier studies showed that the ancestor of this autochthonous steppe element originated in Central Asia during the Miocene/Pliocene, i.e., in the same region and at the same time as the first appearance of steppe vegetation. However, as the extant lineages of Krascheninnikovia ceratoides diversified only 2.2 ± 0.9 Mya, it may represent a modern element of current dry steppe and semi-desert formations, rather than a component of the first steppe precursors of the Miocene. As such, it may have capitalised on the climatic conditions of the cold stages of the Quaternary to expand its range and colonise suitable habitats outside of its area of origin. To test this hypothesis, phylogeographic methods were applied to high-resolution genotyping-by-sequencing data. Our results indicate that Krascheninnikovia originated in western Central Asia and the Russian Altai, then spread to Europe in the West, and reached North America in the East. The populations of eastern Central Asia and North America belong to the same clade and are genetically clearly distinct from the Euro-Siberian populations. Among the populations west of the Altai Mountains, the European populations are genetically distinct from all others, which could be the result of the separation of populations east and west of the Urals caused by the Pleistocene transgressions of the Caspian Sea.

Finding morphological differences between cytotypes that are stable throughout their geographical range is important for understanding evolution of polyploid complexes. The ancient monocot lineage Acorus includes two groups, of which A. calamus s.l., an important medicinal plant, is a polyploid complex with a centre of diversity in Asia. European plants are sterile triploids introduced by humans. An early study suggested that plants from temperate Asia are tetraploids, but subsequent work revealed diploids and triploids rather than tetraploids in Asiatic Russia; however, cytotype diversity in Western Siberia is insufficiently known. We document the occurrence of diploids and triploids in Western Siberia. Triploids that do not differ in genome size from European Acorus are abundant in the valley of the river Ob where the ability for extensive vegetative propagation provides ecological advantages. An isolated population of aneuploid triploids with 33 chromosomes is found outside the Ob valley. Flow cytometry provides an efficient tool for identification of aneuploid plants in Acorus. All triploids are sterile, but their flowers develop uniform parthenocarpic fruits. Fruits of diploids usually vary in size within a spadix depending on the number of developing seeds. In contrast to North America, where the native diploid plants differ from the introduced triploids by the absence of a secondary midrib of the ensiform leaf blade, Siberian diploids are similar to triploids in possessing a secondary midrib. We confirm that diploids differ from triploids in the size of air lacunae in leaves, which is determined by cell number rather than cell size in septa of aerenchyma. A combination of spathe width and spadix length measured after the male stage of anthesis shows different (slightly overlapping) patterns of variation between diploids and triploids in our material.