Open Access
Issue
BIO Web Conf.
Volume 17, 2020
International Scientific-Practical Conference “Agriculture and Food Security: Technology, Innovation, Markets, Human Resources” (FIES 2019)
Article Number 00065
Number of page(s) 4
DOI https://doi.org/10.1051/bioconf/20201700065
Published online 28 February 2020

© The Authors, published by EDP Sciences, 2020

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

1 Introduction

Environmentally friendly plant resources are widely used in the agriculture. Numerous publications provide data on the ecological and physiological role of bacterial preparations that inhabit the rhizosphere and internal tissues of plants. In particular, a positive effect on plant development and grain yield growth has been identified. Their ability to suppress pathogenic microorganisms, contributes to the neutralization of toxins in the soil and the plant, and enhances the digestibility of phosphorus and nitrogen. Associative bacteria can synthesize a number of natural products that are used by the plant itself [1, 2]. Strains of endophytic bacteria reduce the influence of biotic and abiotic factors due to the positive biochemical and physiological effects of the latter on plants [3] Therefore, using the beneficial potential of herbal preparations is an effective resource in increasing the size and quality of the crop, as well as optimizing ecological conditions of the habitat of plants.

The application of microbiologically active preparations for buckwheat is being developed, the development of plants and the yield is subject to the significant influence of climatic stresses. They are especially critical in the zone of the Middle Volga region, when an unfavorable combination of hydrothermal vegetation conditions is observed in the most critical phases of the formation of the plants’ productive potential. Spring drought or the return of cold weather in the early stages of development determines the growth processes of both the root system and terrestrial vegetative organs, reduces the number of reproductive organs. Frequently repeated soil-atmospheric droughts against the background of high temperatures in the middle of the plant vegetation, during flowering and fruit formation, reduce the flight activity of bees and cause the death of a significant part of the formed ovary.

Researchers identified an increase in the agrochemical responsiveness of buckwheat plants during seed treatment with rhizoagrin and flavobacterin [4]. Their metabolic products can inhibit the development of pathogenic microflora, stimulate seed germination and increase their germination [5].

A study by Chinese scientists showed the influence of endophytic fungi from Tatar buckwheat (F.tataricum) on the growth of root hairs of the host and the production of functional metabolites. The authors say that the use of specific fungal pathogens can be an effective strategy to improve the nutritional regime and functional qualities of seedlings of Tatar buckwheat [6].

In the studies conducted on buckwheat (F.esculentum), the use of bacterial fertilizers increased the length of plants, nodes, length, width and the number of leaves in general) [7].

The aim of our research was to study the effect of seed treatment and evaluate the effectiveness of using the Streptomyces sp strain on the growth and development of buckwheat plants.

The gram-positive bacteria influence the soil and plants characterized by a complex secondary metabolism. It is known that they synthesize a large number of antibiotics that can suppress the phytopathogenic microflora. In addition, their metabolites can have a growth-promoting and adaptogenic effect on plants under the influence of stressful conditions, thereby reducing the negative effects of the latter.

2 Material and methods

The experiment was conducted on the experimental site of the agronomical faculty of Kazan State Agrarian University, on gray forest soils with a humus content of 3.2 %, with an increased phosphorus content (145 mg per 100 g of soil) and an average potassium content (110 mg per 100 g of soil) with a pH of 5.3. A suspension of microorganisms Streptomyces sp was given by the Center for Agroecological Research of Kazan State Agrarian University.

Small plot experiments were performed on plots with an area of 5 m2. The technology of tillage and sowing is generally accepted for the Republic of Tatarstan. The seeding rate was 3.0 million pcs. seed per hectare. The Batyr variety used in the Middle Volga region of the Russian Federation was chosen.

The object of study was the Batyr variety, admitted to cultivation in the Middle Volga region of the Russian Federation. The variety is mid-season, has a high potential for seed productivity in comparison with other varieties cultivated in the Republic of Tatarstan, blooms evenly and actively, is bee pollinated. However, in years with the manifestation of extreme vegetation conditions, especially during the formation of generative organs, this variety significantly reduces the plant productivity coefficient due to disturbances in the process of gametogenesis and embryogenesis [8].

The experimental strain of Streptomyces sp. was compared with the control option and the option involving the treatment with Rizoplan biofungicide, chemical protectant “Armor 3” (AI tebuconazole, thiabendazole, imazalil). It is known that Rizoplan can suppress the development of phytopathogens, has a growth-activating and antidepressant effect. It has been tested on a wide range of cultures.

The study options were four standards for making suspension Streptomyces sp: 0.5; 1.0; 1.5; 2.0 l/ha with a flow rate of 200 l/ha. The control preparations were used according to the recommended norms.

The hydrothermal conditions of the first half of buckwheat vegetation were arid. The rainfall deficit amounted to 60 % of the normin May, less than 50% of the norm in June. For this reason, there was a slight lag in growth and branching compared to the favorable years. During the period of mass growing, the average daily temperature exceeded the long-term norm by 2.5 °C. Precipitation was only 37 % of the norm. Thus, in the most critical periods of crop formation, buckwheat plants suffered from a deficit of precipitation.

The following analyzes were carried out: phenological dates of the plant development phases, field germination and ecological stability of plants, plant structure and yield of leaf surface measurements in dynamics, quantity and qualitative composition of chlorophyll, taking into account the yield of experimental options, statistical processing of experimental data.

The study of the dynamics of biomass accumulation, the leaf surface area, biometric parameters of plants, and seed productivity of plants were evaluated according to the generally accepted methods [8].

3 Results and discussion

The maximum field germination (99 %) was obtained when applying 1 liter per hectare (Table 1). A close value (94 %) was obtained for the control option. For other options, this indicator ranged from 70 to 80 %

The ecological resistance of plants to vegetation conditions, expressed as the preservation of plants for harvesting, was maximum (88 %) in the variants with seed treatment with the strain in the amount of 1.5 and 2.0 liters per ton of seeds. In the cases where the field germination of seeds was higher, the plants’ conservation for harvesting decreased to 69...73 % due to more stringent competitive relations.

During the period of mass flowering and at the beginning of fruit formation, on the options with seed treatment by the studied strain, a more intensive growth of plants was noted in length, combined with an increase in the mass of leaf-stem mass, the mass of the reproductive organs and leaf surface (Table 2).

Seed treatment with Streptomyces sp contributed to an increase in the biometric parameters of plants (Table 3).

Activation of plant growth is observed in variants with a low rate of suspension (0.5 and 1.0 l/t). Bacterial treatment with Streptomyces sp. increased the number of nodes, productive shoots of the first order, inflorescences, fruits. The value of these signs increases as the norm increases from 0.5 to 2.0 l/t. When treating seeds with Rizoplan and chemical preparations, plant growth processes were activated, but the number of shoots and inflorescences significantly decreased.

Plant productivity is determined by the quantity and efficiency of photosynthetic pigments, which are responsible for the absorption and conversion of solar energy into the energy of chemical compounds. The biosynthesis of photosynthetic pigments is significantly affected by environmental conditions, including the climatic conditions of the growing season and agrotechnical methods [9], We associated the intensity of production processes with the amount of chlorophyll in the leaves, The data on the dynamics of the chlorophyll biosynthesis “a” and “b” in the leaves of buckwheat are presented in Table 4.

During the period of mass flowering, the biosynthesis of pigments in the leaves of the control and experimental variants was more intensive than during the period of fruit formation, This can be explained by the accelerated rate of transition of plants to a new life cycle, when synthetic processes are replaced by the processes of attraction of plastic elements from the leaves to the fruits, The total amount of chlorophyll decreased by 58 %, in the variants treated with the Streptomyces sp strain – by 32...45 %, When treating with Rizoplan and chemical preparations, this dynamics was not observed.

The biosynthesis of pigments during flowering and intensive growth and development when treating seeds with Streptomyces sp in the amount of 1 to 1.5 l/t of seeds was intensive.

Table 5 presents data on the relative amount of chlorophyll “a” to chlorophyll “b” during mass flowering and fruit formation.

During the mass flowering, this ratio was relatively stable. The amount of chlorophyll “a” exceeded the amount of chlorophyll “b” by 2.5...2.7 times.

In the phase of mass fruit formation, the proportion of chlorophyll “b” increased.

In the modern literature on plant physiology, the role of chlorophyll in the regulation of ontogenesis phases is discussed along with the photosynthetic properties of pigments. Strengthening the synthesis of chlorophyll “b” in the transgenic lines of Arabidopsis thaliana slowed down the rate of plant aging, delaying the processes of transformation of vegetative meristems and the transition of plants to subsequent phases of [10] ontogenesis.

Buckwheat is prone to unproductive growth [11, 12]. In the regions with a short favorable period of vegetation, any delay in the process of fruit formation reduces its productivity [13], Variants with a reduced proportion of chlorophyll “b” accelerated the rate of formation of the reproductive system of plants, thereby increasing their seed productivity.

Table 6 presents the data on total biological productivity and productivity of experimental plots.

According to the data, the total biological productivity of plots treated with biological preparations was inferior to the control variant and the variant involving treatment with chemical preparations, To a large extent, this is due to the smaller number of plants per square meter (see Table 1).

The maximum grain yield in the experiment with 249,7 g/m2 was obtained when applying Streptomyces sp, in the amount of 2,0 liters per ton of seeds, The excess in the grain yield over the control one and the one obtained when treating with a chemical preparation was 53 and 37,5%, respectively, The additional yield was obtained due to an increase in the number of branches and inflorescences, as well as the number of full-fledged fruits.

Table 1.

Field germination and environmental sustainability of buckwheat plants during seed treatment with chemical and biological preparations

Table 2.

The effect of seed treatment on the production potential of plants of the buckwheat Batyr variety

Table 3.

Biometric parameters of buckwheat during seed treatment

Table 4.

The effect of seed treatment with Streptomyces sp. on the dynamics of chlorophyll biosynthesis “a” and “b” in the leaves of buckwheat plants

Table 5.

The ratio of the amount of chlorophyll “a” to chlorophyll “b” during mass flowering and fruit formation

Table 6.

The effect of seed treatment with biological and chemical compounds on the buckwheat biomass and yield

4 Conclusion

The studies showed that in the arid conditions of 2018, the treatment of buckwheat seeds Batyr with Streptomyces sp reduced the field germination, increased the number of nodes and shoots, stimulated the biosynthesis of chlorophyll in the leaves during the period of active plant growth and development, In the leaves of the control option, treatment with Rizoplan and Streptomyces sp (0,5 l/t), increased the proportion of chlorophyll “b”, whose value negatively correlated with productivity.

Based on the data on the regulatory properties of chlorophyll “b”, it can be assumed that experimental variants with a reduced share of this fraction in the total amount accelerated the rate of formation of the plant reproductive system, thereby increasing the seed productivity of plants.

5 Recommendations

To increase the stability of buckwheat crops in regions with spring-summer drought during seed treatment, a bacterial preparation containing Streptomyces sp strains, activating the productive shoots, inflorescences, and full-fledged fruits can be used.

Acknowledgments

The study was conducted with the financial support provided by the Ministry Of Education And Science Of The Russian Federation, The subsidy agreement number is №14.610.21.0017. The unique identifier of the project is RFMEFI61017X0017.

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All Tables

Table 1.

Field germination and environmental sustainability of buckwheat plants during seed treatment with chemical and biological preparations

Table 2.

The effect of seed treatment on the production potential of plants of the buckwheat Batyr variety

Table 3.

Biometric parameters of buckwheat during seed treatment

Table 4.

The effect of seed treatment with Streptomyces sp. on the dynamics of chlorophyll biosynthesis “a” and “b” in the leaves of buckwheat plants

Table 5.

The ratio of the amount of chlorophyll “a” to chlorophyll “b” during mass flowering and fruit formation

Table 6.

The effect of seed treatment with biological and chemical compounds on the buckwheat biomass and yield

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