© The Authors, published by EDP Sciences, 2021

1 Introduction

Identification of the plant development features, the architecture, and the life forms depending on the habitat conditions are one of the promising areas of biodiversity research [1, 2]. Recently, this data has been used to create models of plant responses to climate change, to study the functional traits of populations and communities, and for biomimetic architecture [3, 4]. The objects of such studies are widespread plant species with high morphological variability. In this connection, Thymus L. is of interest. This work is devoted to the study of Thymus mongolicus (Ronn.) Ronn., which is widespread in the mountain steppes of Siberia [5]. The aim of the study is to identify the features of T. mongolicus morphogenesis in the conditions of Southern Siberia.

2 Materials and Methods

The material was collected nearby the village of Aktash (Mountain Altai), in the intermountain basin, in the petrophytic steppe, the total projective grass cover is 50 %, the projective cover of T. mongolicus is 3%. For comparative analysis we used data obtained earlier in the study of T. mongolicus in the Altai and Tuva [6], as well as data by N.M. Pyak [7]. In the study of ontogenesis, the concept of discrete description of ontogenesis was adopted [8]. The phases of morphogenesis are identified according to the works on thestudy of dwarf shrubs [9]. The type of T. mongolicus biomorph is established in accordance with the phytocenotic classification by O.V. Smirnova [10]. The age of the individuals was determined by the annual rings of skeletal axes using the Carl Zeiss SteREO Discovery stereomicroscope.V12 with AxioCam HRc camera (Germany).

3 Results

At the initial stages of ontogenesis (seedling (p), juvenile state (j)), individuals represent orthotropic primary shoot. During autumn germination, the shoot of the seedling is shorted to 0.5 cm long. The next year, in the juvenile state, an elongated annual shoot develops, the further development of the individual coincides with the development of T. mongolicus, described by N. M. Pyak [7], and T. petraeus Serg. [11]. During spring germination in the same year in juvenile individuals, the primary shoot is elongated to 1 cm. Buds are laid in the axils of all the leaves. In the second year, in immature individuals (im), the primary shoot consists of two elongated annual shoots and reaches 2 cm. From the buds in the leaf axils of the first annual shoot, orthotropic shorted (or elongated) vegetative shoots are developed. The primary bush is formed. In the third year, the apical part of the primary shoot dies off. Lateral shoots have monopodially growth, resting and proleptic buds begin to grow on the preserved part of the primary shoot (Table 1). The root system consists of a main root and adventitious roots.

In the fourth year in the virginal state (v), the lateral shoot, which is close in position to the place of death of the apical part of the primary shoot, becomes a replacement shoot and lies down. A plagiotropic acrosympodially main skeletal axis is formed. Similarly, the lateral shoots become from the 1st order. The type of biomorph is monocentric.

The first generative shoots appear in the middle part of the skeletal axes at year 7, the individual passes into a young generative state (g1). At the top of the generative shoot, a capitate thyrse is formed from opposite dichasias. Skeletal axes 2nd and 3rd orders develop in the bush. The plant is a clump consisting of a primary bush and 2–3 partial bushes. The monocentric type of biomorph changes to dense polycentric type. The clump lasts for the entire generative period (from young to old generative states), which is about 14 years. In the mature generative state (g2), vegetative reproduction begins. The separated ramets (partial bushes) are rejuvenated to a virginal or young generative state. Vegetative reproduction prevails over seed reproduction and ensures self-maintenance of T. mongolicus populations. By the age of 19, in the old generative state (g3), the clump breaks up into separate partial bushes that are in the same ontogenetic state. After that, the individual passes into a subsenile state (ss) and is a dilapidated primary bush with several vegetative shoots in the basal part.

4 Discussion

The analysis of the obtained data, their comparison with the data obtained earlier [6, 7] showed the similarity of the morphogenesis of individuals growing in different habitats. However, depending on the shape of the topography, the substrate and the total projective grass cover, T. mongolicus shows a polyvariance of development. The longest duration of ontogenesis is observed in individuals in the petrophytic steppes on the mountain slopes (Table 2). Quickly, already at the 2nd year of development, the individual passes to branching and the primary bush is formed. Self-maintenance of populations occurs due to vegetative reproduction. In petrophytic steppes on the leveled areas of intermountain basins, the duration of ontogenesis of individuals is reduced, and self-maintenance of populations is carried out equally by seed and vegetative reproduction. The duration of ontogenesis of individuals also decreases along the banks of rivers on pebbles and on scree rocky slopes. The curtain is formed already in the virginal state, in the same or in the young generative state, vegetative reproduction occurs. Self-maintenance of populations occurs mainly in a vegetative way. The shortest duration of ontogenesis is observed in individuals in the sandy steppes on the interwoven sandy substrate. The primary bush is formed in the first year, when the primary shoot lies down and begins to branch. Skeletal axes and shoots are intensively rooted, and vegetative reproduction begins in the young generative state. The resulting ramets can be rejuvenated to an immature state.

Thus, the features of T. mongolicus development (different duration of individual ontogenetic states, ontogenesis and morphogenesis phases, the way of self-maintenance of populations) contribute to plant adaptation, survival and distribution of the species in different habitat conditions of Southern Siberia.

The work was carried out with the financial support of the project of the State Assignment of Central Siberian Botanical Garden of the Siberian Branch of the Russian Academy of Sciences No AAAA-A21-121011290026-9.

References

All Tables