Rhaponticum integrifolium is a perennial often herbaceous plant. Stem 60 - 150 cm (Figure 1). Basket spherical 4.5 - 6.0 cm in diameter. Corollas pale yellowish, at the end of flowering pale orange. Achenes are inversely ovate, glabrous, milk-white. The bristles of the tuft with grooves exceeding the diameter of the bristle more than 3 - 4 times, cream. Length 0.8 - 1.0 cm, width 0.3 - 0.5 cm.

LATENT PERIOD. Seed sizes common in different geographical latitudes and longitudes of individuals Rh. integrifolium differ sharply from each other. (Chodak: length 0.9 ± 0.25 cm, width 0.25 ± 0.11 cm, weight of 1000 seeds 22.5 ± 0.67 g; Gilan: length on average 1.1 ± 0.15 cm, width 0.37 ± 0.13 cm, weight of 1000 seeds 23.5 ± 0.94 g) (Table 1).

In laboratory conditions, the temperature increase from 18˚C to 28˚C has a positive effect on the germination of Rh. integrifolium seeds. It was found that the germination of plant seeds is very sensitive to the process of stratification (27% - 33%). In the field, the maximum germination of Rh. integrifolium seeds is observed when planting in October-November in a mechanically processed, refrigerated form (68% - 75%). In such conditions, the seed germinate 20 - 25 days earlier compared to untreated seeds in favorable weather conditions and forms the root system to increase air temperature and drainage of 10 - 20 cm of the soil horizon.

VIRGINALLY PERIOD. 1-year. Stage sprout (p). The germination of Rh. integrifolium aboveground, from the seed germinates primary (main) root. After reaching the length of the root to 1.5 - 2 cm, rapidly developing cotyledon leaves rise to the soil surface. The length of the new cotyledon leaves 1.5 - 2 cm, width 0.6 -0.7 cm.

From the first time, plants 20-25 April formed true leaves in the middle of cotyledon leaves. By this time, the root system of the seedling is formed and reaches 6 - 9 cm. In natural conditions, 2% - 3% of the seedlings are preserved. However, in the experimental plots with the help of appropriate agrotechnical measures, this figure is achieved up to 80% - 85%.

Juvenile stage (j). The plant passes to the juvenile stage in 20 - 24 days. This stage is justified by the formation of 6 - 10 basal leaves, the emergence of a new underground organ—the stem, the active formation of roots and the formation of dormant buds at the root. At the beginning of the stage, after 3 - 5 days after the formation of the first coming leaf, the second real leaves appear. Further formed leaves Rh. integrifolium compared with the previous leaves differ in the size of the petiole and leaf blade and accelerated development.

At the juvenile stage, one of the important morphological changes observed in the plant is the thickening of hypocotyl and the formation of additional roots formed in the internal tissues. At the same time, an underground organ is formed—a stem with a new functional structure. At the juvenile stage in the aboveground part of the stem, in the lower center of the leaf petioles 2 - 6 cone-shaped buds are formed-developing in the spring of next year.

Vegetation Rh. integrifolium continues from the end of July to the first decade of August and ends its vegetation with the formation of up to 6 - 7 basal leaves in each individual.

During the studies in the first year of vegetation Rh. integrifolium no signs characteristic of the immature stage were observed. In our opinion, the absence of the immature stage in the conditions of Uzbekistan in the first year of vegetation is associated with the manifestation of morpho-biological adaptations to arid conditions of the territory with the acceleration of the stages of ontogenesis of plants in hot weather conditions. Such morpho-biological adaptation is also manifested by the activity of above-ground and underground parts of plants growing in the conditions of Chodak (1000 - 1200 m above sea level) and Gilan (2200 - 2400 m above sea level) In particular, the plants growing in the experimental areas of Gilan are characterized by the active development of underground organs, and growing on the territory of Chodak—by the active development of above-ground organs—leaves, in addition to the number of regenerating buds.

2-year. Virginile stage (v). In the great life cycle of Rh. integrifolium, virginile or mature stage lasts up to 3 years (Table 2). The stage is characterized by the complete formation of vegetative organs, increased biomass, the formation of these rosette leaves from the stem and the strong development of the root system (Figure 2).

The appearance of tuberous extensions 12 - 15 cm of the main root in the third year virgin stage is of particular importance. Tuberous part of the root remains till the end of the year virgin stage and 2-phase generative period disappears as a result of intensive development of the main root.

GENERATIVE PERIOD. Young generative plants (g1). The first renal escape Rh. integrifolium passes to the generative period in the second year of vegetation. If we compare with the number of individuals, in the third year of vegetation 7% - 8% of plants pass to the generative period, in the fourth year 75% - 80%, 5-year 10% - 12% (Figure 2, Table 2).

Most generative shoots formed in the third year of vegetation do not pass the full cycle of development. In most individuals, there is a weakening of the development of internodes in the early stages of generative shoots, which leads to drying of inflorescences. Only a small number of generative shoots 10% - 15% can reach the flowering phase. On experimental plots Gilan and Chodak for 3 - 4 years of vegetation in each plant is formed by 1 generative shoot. If the length of the generative shoot formed in the first year of vegetation is low (20 - 28 cm), then in subsequent years it exceeds (70 - 90 cm) the vegetative shoot (Table 2). One of the main features of the first generative stage is the increase in the number of storing kidneys. Their increase is observed, especially in the 4th year of vegetation, which ensures the transition of plants to the Mature generative stage (g2).

Middle-aged generative plants (g2). Rh. integrifolium from 5 years of vegetation goes to the generative mature stage and lasts up to 10 years of growth. A 5-year vegetation 40% - 45% of the plants, and 6 - 7 year growing season 100% of plants are move on to a full generative mature stage. At the same time, up to 6 - 10 generative shoots can be formed. In the 2 - 4 upper nodes of the Central generative shoot, the formation of 2 generative branches and the formation of additional inflorescences in them is observed. However, the inflorescences formed in the Central generative shoot differ in a smaller volume from the other inflorescences (Table 2, Figure 2). Despite the maximum value of all the morphological parameters of the Rh. integrifolium, at the mature generative stage, the formation of particulates begins, which determines the transition of the plant to the senile period. At the g2 stage, 10% - 15% of plants form a particula.

Old generative plants (g3). To 9, and especially 10 - 11 year vegetation of Rh. integrifolium, weakens the formation of vegetative and generative organs. Reducing the number of rosette leaves, buds, generative shoots, reducing the volume of inflorescences and leaf blade and most importantly—the rotting of the root indicate the transition of the plant to the old generative stage. At this stage Rh. integrifolium begins its vegetation 15 - 20 days later in comparison with early vegetating plants and the formation of generative shoots is carried out at the expense of old generative polycyclic shoots. They number no more than 1 piece, and the height is much lower (18 - 20 cm) than vegetative shoots (Table 2, Figure 2).

In the old generative age, the formation of particulates is accelerated and is 2 - 3 pieces. In Rh. integrifolium the old generative stage lasts 3 - 4 years. Despite the weakening of all morphological features, plants at this stage are characterized by an increase in the diameter of the outlet from the aboveground part and the diameter of the base of the main root, in addition, this trend continues almost until the end of the senile period.

Senile period. The previous stage of the senile period(s)—the subsenile stage (ss) begins in 13 - 14 years of vegetation Rh. integrifolium and accelerated in the 15th year of vegetation. At the same time, the habitus of the plants is highly reduced, the flange is thickened at the expense of the partucula and the top of the main root is also being consolidated. Usually Rh. integrifolium finishes its vegetation in 17 - 18 years, but some individuals of the plant die in 20 - 21 years.

General vegetation Rh. integrifolium on the experimental plot Gilan equal 125 - 135 days, and on the experimental plot Chodak 100 - 115 days. For budding will require 10 - 15 days of the growing season, flowering is 24 - 26 days (Chodak 20 - 21 days), for the formation of seeds 30 - 35 days (the Chodak—25 - 30 days) for maturation of seeds 25 - 32 days (Chodak 20 - 22 days).

The beginning, end and duration of phenological phases of the plant are associated with air temperature, soil moisture and ontogenesis periods. Air temperature rise in relatively flat areas in 1000 - 1200 m above sea level affect the reduction of phenological phases (Chodak) or wet weather and relatively low temperatures of 2200 - 2400 m above sea level affect the duration of phenological phases (Gilan). In addition, with the approach to the middle age period of the plant there is a relatively early start of phenological phases and this is probably due to the characteristic biological characteristics of the plant.

The real seed productivity (RSP) Rh. integrifolium is 2 - 4 times less than the potential seed production (PSP), which indicates the ability to reproduce in adverse conditions. If we compare the plants in the experimental plots Chodak and Gilan (Table 3), we can see high rates of RSP in the g1 stage in plants growing on the Chodak, g2 stage in plants on the territory of Gilan.

Quality seed ripening Rh. integrifolium observed on site Gilan. This is due to the high coefficient of productivity in all generative stages compared with plants growing on the territory of Chodak (Table 2). The high coefficient of productivity of plant seeds in the territory of Gilan confirms that Rh. integrifolium grows in optimal conditions of its area.

In Uzbekistan the location of Rh. integrifolium observed in Surkhandarinskaya region (mountain of Hojagurgurata), Boysun mountains (the village Gilon and Kul), on the slopes of the Gissar and Turkestan ranges (neighborhood villages of Urgut and Madm), in Tajikistan—on the slopes of the Gissar (lane Anzob, Khodjdobigarm, a neighborhood of village Tagob, surrounds the cities of Kulyab, Shurabad) and Darvaz ranges (neighborhood villages Tavildar, Kildare and Sagirdasht). In Kyrgyzstan, the Rh. integrifolium habitat occupies the North-Western part of the Fergana ridge and the slopes of mount Baubashata (gorge of the rivers Kugart and Shaydansay).

Sh.G. Ganiev (1980) for the first time described only two associations involving Rh. integrifolium in the North-East of the area (Kyrgyzstan) and identified reserves of the aboveground part of the plant on an area of 25 hectares, which were: leaves—23 centner, inflorescences—5, roots—10 centner.

We studied the role of Rh. integrifolium in the composition of vegetation on the slopes of Gissar mountain ridge, within the Kashkadarya region; described 11 associations in which boljshegruzy Manchurian participates as edificatory or sub edificatory in the composition of the formations of the Acer turkestanicum, Amygdalis bucharica and Rhaponticum intеgrifolium:

I ACER TURKESTANICUM FORMATION. Associations: 1.1. Acer turkestanica + Agropyron trichophorum + Rhaponticum integrifolium + Рrangos pabularia; 1.2. Acer turkestanica + Rhaponticum integrifolium + Eremurus regelii + Rheum maximowiczii; 1.3. Acer turkestanica + Rhaponticum integrifolium.

II AMYGDALIS BUCHARICA FORMATION. Associations: 2.1. Amygdalis bucharica + Prangos pabularia +Rhaponticum integrifolium + Ferula kuhistanicа; 2.2. Amygdalis bucharica + Eremurus regelii + Rhapоnticum integrifоlium + Bromus inermis; 2.3. Amygdalus bucharica + Agropyrоn trichophorum + Rheum cordatum + Rhaponticum integrifolium; 2.4. Amygdalus bucharica + Poa nemoralis + Strigosella trichocarpa + Rhaponticum integrifоlium.

III RHAPONTIUM INTEGRIFOLIUM FORMATION. Associations: 3.1. Rhapontium integrifolium + Rumex paulsenianus + Carex pachystylis + Allium suworowii; 3.2. Rhapоnticum integrifolium + Rheum cordatum + Eremurus robustus + Rosa kokanica; 3.3. Rhaponticum integrifolium+ Inula grands + Prangos pobularia + Bromus oxyodon; 3.4. Rhaponticum integrifоlium + Cerasus mahaleb + Ferula kuhistanica + Poa bulbosa.

Observations show that a significant part of the territory of the Rh. integrifolium formation is used by the local population, mainly for the preparation of hayfields for cattle. For this reason, before the end of July, i.e. before the harvest of hayfields and small horned cattle here are not available. As a result, there is a possibility of self-seeding walleye. In our opinion, perhaps this contributed to the emergence of optimal conditions for germination of this plant. This, on the one hand, testifies to the positive role of anthropogenic impact in the preservation of Rh. integrifolium formation communities.

Site Gilan, Kizilemgac, Kul, Hisarak located in the vicinity of Tanhazdarya river in the foothills of the Hissar mountains dominate the area and natural resources of plants. In other words, 98% of the total Rh. integrifolium distribution in the republic and 88% of the total natural resource plants is located in the vicinity of these geographical points.

The yield of the aboveground part in the associations that make up the price complex Rh. integrifolium ranges from 210 to 950 kg/ha (Table 4).

The studied massifs with the participation of Rh. integrifolium were divided into three categories depending on the yield, the degree of remoteness from settlements and roads. The massifs of the 1st category include thickets that are easily accessible for the collection of raw materials and convenient for its transportation due to the proximity to roads. Massifs of thickets of the 2nd category are farther (on 8 - 10 km) from highways in comparison with the first category and on higher and less accessible slopes. Massifs of the 3rd category are removed from highways on considerable distance—12 - 20 km and more. Delivery of raw materials to cars is possible only with the help of pack transport.

The results of determining the areas of arrays and reserves of raw materials Rh. integrifolium in the Hissar range within Uzbekistan are shown in Table 5. As can be seen from the table, the 1^st category of thickets occupies a leading position in the total area (125 hectares, or 52% of the area of all surveyed arrays). The share of less productive and less suitable for harvesting raw materials (category 3) thickets is slightly more than 22%. The most promising for the development are investigated in the thickets surrounding villages Gilon, Khisorak and Kizilimgak.

The results of experiments to determine the rate of recovery of above-ground phytomass Rh. integrifolium using single-factor analysis of variance [29] are presented in Table 6. In the first year after cutting, the recovery of phytomass occurs due to dormant kidneys. In this generative shoots appear only in the second year of vegetation. Annual cutting of shoots Rh. integrifolium (option III) showed that the number of shoots and their height decreased by more than 69%, a strong change was observed in the yield of phytomass, which decreased to 72% at the end of the experiment. In the experiment with a break in the workpiece in one year (option II) Rh. integrifolium oppression is also clearly expressed, the number of shoots and their weight on the test sites were lower than in the control. Yields during the experiment fell by 20% (was 50.3, was 40.2 g/10m²). In the variant of the experiment with “rest” in two years after cutting (option I), the recovery of shoots was 91, and phytomass—88%.

Comparison of the results of the experience in the restoration of the above-ground parts of the plant in different variants allows us to conclude that the mode of operation of the plant thickets with a break of three years provides a complete restoration of the raw phytomass Rh. integrifolium. However, we recommend that this period be extended by another year to guarantee a reliable recovery of the phytomass, i.e. the raw material in the same array should be harvested only four years after the previous one. Breaks in the blanks Rh. integrifolium in the same array should be at least five years, and the volume of annual blanks should not exceed 20% of its operational reserve.

To determine the optimal timing of preparation of medicinal raw materials as a source of ecdysteroids (20-hydroxyecdysone) is necessary to know the dynamics of their accumulation in individual plant organs by phases of development. The obtained data on the quantitative content of 20-hydroxyecdysone in different parts of plants cultivated in the Fergana region and in the vicinity of Gilon village of Kashkadarya region are given in Table 6. As can be seen from the above data, depending on the phase of development and part of the plant, the content of 20-hydroxyecdysone varied from 0.21% to 1.42%. The maximum value recorded in the fruit—1.42%, in the roots early in the growing season—89%, and in the aerial part at the flowering stage—0.98% (Chodak, Fergana region). In the vicinity of the village Gilon Kashkadarya region the content of 20-hydroxyecdysone was from 0.06% to 2.0%, the maximum was fixed in the roots—2.0% and in the above-ground part in the flowering phase—0.9% (Table 7).

Note. Category I—thickets easily accessible for the collection of raw materials and convenient for its transportation due to the proximity to roads; category II—thickets are 8 - 10 km from roads and on higher and less accessible slopes; category III—thickets are removed from roads by 12 - 20 km or more.

Note. Option experience: I—two years of “rest” after cutting shoots; II—one year of “rest” after cutting shoots; III—annual cutting shoots; control— without cutting shoots.