Notes on the taxonomy and distribution of species of the Dryopteris dilatata complex in the Caucasus, Siberia and the Far East

The Dryopteris dilatata complex in the Caucasus, Siberia and the Far East was studied on the herbarium material from the Komarov Institute of Botany in Leningrad. The macromorphological characters of the sporophyte as well as the morphology and colour of spores were used. It has been found that Dryopteris extremiorientalis V. Vasil., regarded as an endemic taxon for the Far East, is conspecific with Dryopteris assimilis S. Walker, and Dryopteris Alexeenkoana Fom., regarded as a West Caucasian endemic species is identical with Dryopteris dilatata (Hoffm.) A. Gray, em. S. Walker. In .the paper the distribution of D. assimilis in the Asiatic part of the USSR was given

Staminodial Nectary Structure in Two Pulsatilla (L.) Species

In plants belonging to the Ranunculaceae the floral nectaries may differ in origin, location in the flower, shape and structure. In many cases they are defined as modified tepals or modified stamens. The nectary organs in this family are frequently termed "honey leaves," and staminodial origin is attributed to them. Gynopleural and receptacular nectaries are rarely found in Ranunculaceae. To date there are no reports on the structure of the nectary organs in plants of the genus Pulsatilla. We used light and scanning electron microscopy to study the location and structure of the nectaries in Pulsatilla slavica and P. vulgaris flowers. The staminodial nectaries were found to be nectar-secreting organs. The number of stamens per flower (102-398) increases with plant age. The share of staminodes is 12–15%. The staminodes are composed of a filament and a modified head. They are green due to the presence of chloroplasts in the epidermal and parenchymal cells. The parenchymal cells are in a loose arrangement. Stomata (3–20), through which nectar exudation occurred, were found only in the abaxial epidermis of the staminode head. The stomata are evenly distributed and have well-developed outer cuticular ledges. Some of them are immature during nectar secretion, with their pores covered by a layer of cuticle. During the activity of the nectariferous organs in the flowers, primary (on the staminode surface) and secondary nectar (at the base of tepals) are presented. The staminodes of the two Pulsatilla species show similar structural features and have similar shares in the androecium

Genetic diversity in widespread species is not congruent with species richness in alpine plant communities

The Convention on Biological Diversity (CBD) aims at the conservation of all three levels of biodiversity, that is, ecosystems, species and genes. Genetic diversity represents evolutionary potential and is important for ecosystem functioning. Unfortunately, genetic diversity in natural populations is hardly considered in conservation strategies because it is difficult to measure and has been hypothesised to co-vary with species richness. This means that species richness is taken as a surrogate of genetic diversity in conservation planning, though their relationship has not been properly evaluated. We tested whether the genetic and species levels of biodiversity co-vary, using a large-scale and multi-species approach. We chose the high-mountain flora of the Alps and the Carpathians as study systems and demonstrate that species richness and genetic diversity are not correlated. Species richness thus cannot act as a surrogate for genetic diversity. Our results have important consequences for implementing the CBD when designing conservation strategies