Berries, with their high antioxidant capacities, are among the healthiest fruits for human beings. Moreover, they have a unique flavour, colour and diverse content of vitamins and minerals (Pereira et al., 2018; Gündeşli et al., 2019; Okatan, 2020). Commercially important berries are strawberries, blueberries, blackberries, raspberries, red currants and blackcurrants. Berry fruits can be consumed fresh or processed in the form of jams, cakes or pies. Red currant (
The red currant market is mostly dominated by European originated cultivars including ‘Jonkheer van Tets’, ‘Hollandische Rote’ (‘Prins Albert’), ‘Viksne’, ‘Rosetta’, ‘Rovada’, ‘Rolan’ and ‘London Market’, some old Russian cultivars like ‘Natali’ and ‘Shchedraya’ and few American cultivars, i.e. ‘Red Lake’. Besides the climatic adaptation of cultivars, resistance to gooseberry mildew (
Production of crops in a range of environmental conditions is as important as high yield for ensuring food security on the earth. Therefore, the adaptation of different cultivars/genotypes into different environmental conditions is very important for food security. However, global climate change with extreme precipitation events, increase in temperature and drought in some places has been significantly impacting the plants’ adaptation and growth in different environments (Myhre et al., 2019; Kusmec et al., 2021). Changes in CO2 concentration, precipitation and temperature also affect the growth, survival and spread of pathogens and indirectly impact crop cultivation (Zavala et al., 2008; Heeb et al., 2019). Thus, production of non-adapted cultivars in such conditions makes it difficult to obtain a high yield and requires more input. Thus, excessive use and misuse of the inputs may cause environmental degradation and induce global climate change. The plant response to climate change and to stresses is complex and includes changes at both the biochemical and physiological levels (Kumar et al., 2019; Kapoor et al., 2020). It is necessary to consider cultivar-specific physiological and biochemical reactions of plants that directly participate in the formation of adaptation processes in a particular climatic zone for a better identification of resistance in berry crops during breeding. Quite often, the consequences of drought can be seen visually as withering of leaves, reduced plant growth, shedding of the ovary and berries and decline in yield (Kawecki et al., 2006; Grabowski et al., 2009; Olen et al., 2016). Therefore, in breeding programmes, nowadays, breeders aim at adapting crops to multiple factors and climate change (Ceccarelli and Grando, 2020). On the one hand, breeders include abiotic stresses, especially drought and high temperature, and biotic stresses (the pathogens) together for them to characterise and analyse their multiple objectives. The available literature demonstrates that mainly single elements of adaptation have been studied on berry crops such as black currant, raspberry and strawberry, and data were found on some cultivars of red currant (Golyaeva and et al., 2020; Panfilova et al., 2021). According to Bratsch and Tech (2009), currant is a very sensitive crop to drought. In some black currant cultivars, the effects of drought led to a decrease in dry matter, water content, water loss and transpiration (Cosmulescu et al., 2008; Čereković et al., 2013; Netzer et al., 2019). The relationship between water exchange and drought stress was also noted for several other berry crops (Klamkowski and Treder, 2008; Morales et al., 2013; Álvarez-Herrera et al., 2019). This is mostly accepted as the initial response of adaptation mechanisms to drought stress (Chartzoulakis et al., 2002; Guerfel et al., 2009). In the present study, the growth, drought tolerance and biochemical characteristics of some introduced cultivars (‘Jonkheer van Tets’, ‘Hollandische Rote’ and ‘Viksne’) and some selected Russian cultivars and genotypes (‘Shchedraya’, ‘Natali’, 129-21-61, 111-19-81, 261-65-19 and 271-58-24) were evaluated to provide complete information about cultivar resistance in the growing zone to farmers.
The present study was conducted on a loamy haplic Luvisol soil located in the zone of temperate continental climate between May and July from 2013 to 2018 in the Central Chernozem area of Russia. Characteristics of the soil were analysed separately at a depth of 0–200 mm and 200–400 mm according to the standard methods (Mineev, 2001). The thickness of the humus horizon was 300–550 mm. In the horizon with a thickness of 0–200 mm, the soil organic matter (OM) was 2.14% ± 0.08%, soil pH was 5.40 ± 0.15 and available elemental concentrations of potassium and phosphorus were 182.50 ± 62.75 mg · kg−1 and 208.74 ± 27.6 mg · kg−1, respectively. Furthermore, in the soil horizon with a thickness of 200–400 mm, the soil OM was 1.85% ± 0.06%, soil pH was 5.5 ± 0.2 and available elemental concentrations of potassium and phosphorus were 125.42 ± 38.65 mg · kg−1 and 149.12 ± 24.34 mg · kg−1, respectively. The climatic characteristics of the study site during the experimental research are given in Table 1.
Some climatic characteristics of the experimental site.
Year | Average monthly air temperature (°C) | Humidity (mm) | Maximum soil temperature (°C) | |||
---|---|---|---|---|---|---|
May | July | May | July | May | July | |
2014 | 16 | 19.1 | 37.1 | 20 | 46.6 | 53 |
2015 | 19.5 | 20.8 | 44.2 | 79.1 | 56 | 46 |
2016 | 17.7 | 21.2 | 47.2 | 66.5 | 34.5 | 31 |
2017 | 16.3 | 22.2 | 56.3 | 85.5 | 38.5 | 41 |
2018 | 17.7 | 21.2 | 31.4 | 120 | 42 | 29 |
Long-term average | 13 | 18.5 | 36.3 | 88.8 | N/A | N/A |
Besides the above given climatic data, the water availability of the region was also calculated according to the formula of Chirkov (1986) to find out optimal and drought seasons. The water availability was estimated as the value of the hydrothermal coefficient (K).
In the above formula, R represents the amount of precipitation in millimetres and Σt is the sum of temperatures above +10 °C for the same period. A lower K value means drier area. The hydrothermal coefficient (K) of the experimental site during the study period is given in Table 2. According to the results obtained, the years 2016 and 2017 had optimal conditions, whereas other years had drought conditions. Therefore, the growth of biochemical characteristics of the red currant plants in current study were tested and compared separately for optimal and drought seasons.
Hydrothermal coefficient of the experimental site during the study period.
Period | 2014 | 2015 | 2016 | 2017 | 2018 |
---|---|---|---|---|---|
May | 0.27 | 0.81 | 1.21 | 1.11 | 0.62 |
July | 0.34 | 0.98 | 1.05 | 1.25 | 0.94 |
К > 1.3 represents excessive hydration; К = 1.0–1.3 represents optimal hydration; К < 1.0 represents insufficient hydration
In this study, three introduced cultivars (‘Jonkheer van Tets’, ‘Hollandische Rote’ and ‘Viksne’) and five Russian cultivars or genotypes (‘Shchedraya’, ‘Natali’, 129-21-61, 111-19-81, 261-65-19 and 271-58-24) were tested. More information about the cultivars and genotypes is presented in Table 3. The site was planted in October 2010. A randomised complete block design (RCBD) with three blocks (replications) was used in the present study. A total of 40 registered plants were arranged in each replication according to the scheme with 0.5 × 2.8 m dimensions. During data collection, 10 plants from each replication were used. The soil in the row spacing was kept under black steam during the research period. No irrigation was performed during the growing period. Once a year (spring, early April) ammonium nitrate (NH4NO3) was applied under the plants. After the occurrence of pests and diseases, chemical control was performed. Penconazole (C13H15Cl2N3) was used against
Introduced and Russian red currant genotypes of the present study.
Genotype | Origin | |
---|---|---|
Genetic | Geographic | |
Jonkheer van Tets | Faya Plodorodnaya × London Market | The Netherlands |
Natali | Russia | |
Hollandische Rote | The Netherlands | |
Viksne | Latvia | |
Shchedraya | Faya Plodorodnaya × Houghton Castle | Russia |
129-21-61 | Jonkheer van Tets × Hollandische Rote | Russia |
261-65-19 | Jonkheer van Tets × |
Russia |
111-19-81 | Jonkheer van Tets - free pollination | Russia |
271-58-24 | Jonkheer van Tets × |
Russia |
The selected forms (129-21-61, 111-19-81, 261-65-19 and 271-58-24) were obtained by us in the Russian Research Institute of Fruit Crop Breeding (VNIISPK) currant breeding laboratory. These genotypes were obtained in 2007 by the method of combinative selection using intersort crosses of red currants of various genetic and geographical origins. For 3 years (2007–2010), field surveys were carried out on a set of economically valuable indicators (the degree of flowering, fruiting, weight accounting of the harvest, the state of plants after winter). Based on the results of the field assessment, four genotypes were selected for further laboratory studies. ‘Jonkheer van Tets’, ‘Hollandische Rate’ and ‘Viksne’ were obtained as cuttings from the Federal State Scientific Institution ‘I. V. Michurin Federal Scientific Center’ (Michurinsk, Russia). ‘Natali’ and ‘Shchedraya’ were also obtained as cuttings from the Federal Horticultural Centre for Breeding, Agrotechnology and Nursery Russian Federation.
During the growing seasons, observations were done on each genotype about the disease resistance/sensitivity of the genotypes. The percent of disease scores (Table 4) were used for the observation of powdery mildew of red currants (
Disease scores followed for the observation of
Disease score | ||
---|---|---|
0 | No infection (healthy plant) | No infection (healthy plant) |
1.0 | Very weak disease damage (up to 10% of leaves and up to 1% of berries are affected) | Very weak damage (up to 5% leaves are affected) |
2.0 | Weak plant disease (up to ¼ of the shrub shoots, up to 25% of leaves and up to 3% of berries are affected) | Weak plant damage (up to 10% of the leaves are damaged) |
3.0 | Average plant disease (up to ⅓ of the shrub shoots, 26–50% of the leaves and up to 10% of the berries are affected) | Average plant damage (up to 30% of leaves are damaged) |
4.0 | Severe plant disease (⅓ to ¼ of the shrub shoots, 51–70% of the leaves and up to 20% of the berries are affected) | Severe plant damage (up to 50% of the leaves are damaged) |
5.0 | Very severe disease (more than ½ of the shrub shoots, more than 70% of the leaves and more than 20% of the berries are affected) | Very severe damage (more than 50% of the leaves are damaged) |
Harvesting of fruits had been performed from 1 to 10 July every year. Productivity was determined from three accounting plants of the same genotype in each replicate. The total yield of each genotype had been calculated and counted to present as tonne per hectare. The length of the raceme was measured from 10 accounting plants from each replication of each genotype. To determine the average weight of one berry, a sample of 100 berries from one genotype was weighed on a technical scale (Scout Pro SP202, Ohaus, USA) and divided by 100. Berries were picked without choice.
For biochemical analysis of berries, 300 g (from each genotype) of ripe berries was collected from 10 accounting plants of each replication. Samples (berries) for biochemical composition analysis were collected from 1 to 10 July in each season. The soluble solids concentration (SSS (sum sucrose soluble) – % Brix) of the fruits was determined by using a digital refractomer PAL-3 (ATAGO, Tokyo, Japan). The content of the sum of sugars (sucrose + monosaccharide) was determined by the weight method according to Bertrand's method (Kumar et al., 2014). Titratable acidity (%) was measured by titration with 0.1 M NaOH solution in the presence of a phenolphthalein indicator. Ascorbic acid content (100 mg · g−1) was then determined by the iodometric method based on the titration of ascorbic acid in coloured extracts with potassium iodate (KIO3) in an acidic medium in the presence of potassium iodide (KI) and starch. Finally, the total phenolic content (100 mg · g−1), which was the total sum of contents of anthocyanins, leucoanthocyanins and catechins, was determined by a colourimetric method using a photocolorimeter photometer KFK3-‘3OM3’ (Zagorsk Optical and Mechanical Factories, Sergiev Posad, Moscow Region, Russia).
The studies were carried out in dynamics from 25 to 30 May and from 20 to 25 July. The intensity of transpiration was determined in the field by using a VT-500 torsion balance (Central Research Textile Institute, Russia) from 11:00 to 12:00. The first weighing measurement was carried out immediately after cutting the leaf (a), and the second one (b) was carried out after 2 min: this made it possible to measure the level of transpiration at the state of saturation of the leaf with water. To determine the level of transpiration, the leaf area was taken into account. The area of the leaf (S) was determined by die cutting using a cork drill with a diameter of 1.0 cm; five die cuts were made from one leaf. The central vein and leaf plate were included in the sample. Then, the following formula was used to calculate the level of transpiration (I):
a – initial weight of the leaf (mg) b – leaf weight in 2 min (mg) t – exposure time (h) S – leaf area (m2)
The content of free and bound water in the leaves was determined according to the Okuntsova-Marinchik method (Voskresenskaya et al., 2008). The method is based on a change in the concentration of a sucrose solution when a leaf sample is immersed in it. Test tubes with stoppers were used. They were weighed; then, 2 ml of 30% sucrose solution was poured and weighed again. Next, 2 g of crushed leaves was placed in a sucrose solution and weighed. After 2 h, the refractive index of sucrose solution was determined in test tubes with plants using a PAL 1 refractomer (ATAGO, Tokyo, Japan). At the same time, the dry leaf mass (for bound water determination) of red currant cultivars was determined. Metal containers with a volume of 70 ml were used. A leaf sample (10 g) was placed and dried in an artificial climate chamber ‘Espec’ PSL-2KRN (ESPEC, Osaka, Japan) at 105 °C for 3 h. The containers were then placed in a desiccator with CaCI2 for cooling and then weighed. The total water content (%) (WC.in.L) of the leaves was then calculated by taking the sum of free and bound water percentages. The coefficient of bound water (%) / free water (%) in leaves was calculated by taking into account the calculated ratio.
Annual measurements were done for the determination of soil moisture and absolute soil moisture. The field soil moisture was estimated at a depth of 0–200 mm and 200–400 mm by drying the soil samples to a constant weight at a temperature of 105 °C and then weighting on a Scout Pro SP202 technical scale (OHAUS, Parsippany, NJ, USA). Calculations were made according to the following formula (Mineev, 2001):
In the above formula, W is the soil moisture (%), a is the mass of water evaporated during drying (g) and b is the mass of dry soil (g). Then, the following formula was used for the calculation of the absolute soil moisture (W1):
The comparison of the studied genotypes was done according to the studied characteristics (disease resistance, biochemical composition, water regime, yield and etc.). The raw data of each parameter were subjected to analysis of variance (Draper and Smith, 2016) by using SPSS, version 22.0, and Excel software programmes. To characterise the indicators of the variation series, the mean value (M), standard deviation (σ) and significance level (
The breeding programme at the institute is designed in such a way that the selection process is preceded by a genetic and statistical analysis of the studied quantitative traits. Therefore, the effectiveness of breeding experiments increases with a smaller volume of hybrid material. It is of great importance to determine the size of the selection of economically useful traits, which require a large cost to analyse. In the course of the work, combinations of crossing (interspecific hybridisation) of cultivars of European origin and species of red currants were carried out. The involvement in breeding practice of other species besides the cultivars of European origin reduced the quality index of berries. In the course of the study, several hybrid families were studied, including >30 seedlings, and such a number allowed us to analyse the inheritance of biochemical and economic-biological traits and to identify valuable genotypes (selected forms) for further study. In this experiment, the samples obtained on the basis of the descendant of the large – fruited
Lesions of
Berry weight, yield, raceme length and the number of berries in a raceme are among the most important characteristics for the determination of productivity and economics of berry production. The data about these parameters are presented in Figure 2.
In terms of berry weight, a significant difference was observed among the test genotypes, where drought season only affected ‘Jonkheer van Tets’ and had no impact on other genotypes. Although there is no significant difference between the berry weights of optimum and drought seasons, the drought season fruits had slightly less berry weight than the optimum season fruits. The highest berry weight was noted in the 261-65-19 genotype (0.65 g), followed by the 129-21-61 genotype (0.61 g). The lowest berry weight was noted in ‘Viksne’ (0.36 g). Besides berry weight, the total yield is also a very important indicator of productivity. Contrary to the berry weight, the yield was found to be significantly affected by the drought season. Thus, the yield of each genotype was found to be significantly higher in optimum seasons than in drought seasons. Moreover, it was also noted that the berry weight alone is not a good indicator of productivity, where the 261-65-19 genotype, which has the highest berry weight, was noted to have a moderate yield, and the highest yield was obtained in ‘Hollandische Rote’ (15.6 t · ha−1). And the lowest yield was observed in the 111-19-81 genotype (5.2 t · ha−1). The yield is also so related with the raceme length and number of berries in a raceme. Evaluation of such characteristics showed that the 271-58-24 genotype has the highest raceme length (10.9 cm), while ‘Shchedraya’ has the lowest raceme length (5.3 cm). Growing conditions were also noted to have a significant influence on the raceme length, and the highest raceme length was measured from plants growing under optimal conditions. Growing conditions had a similar impact on the number of berries in a raceme. Finally, the highest number of berries in a raceme was observed in the 271-58-24 genotype (13.6), and the lowest number was noted in ‘Shchedraya’ (7.2). A great economic value for farmers is not only the length of the raceme, the number of berries in a raceme, the weight of the berry and the yield, which are the components of productivity, but also the biochemical composition of the berries. The marketing policy in the sales markets is determined by the appearance of agricultural products, and in particular, for red currants, the length of the raceme, the number of berries in a raceme and berry weight are the appearance characteristics. Therefore, many breeding programmes for red currants are focussed on these characteristics. The biometric analyses made it possible to divide the studied genotypes into several groups according to the criteria developed by Knyazev and Bayanova (1999) (Table 5).
Biometric indicators of productivity components.
Genotypes | Raceme length | Number of berries in a raceme | Berry weight | ||||||
---|---|---|---|---|---|---|---|---|---|
Short (5.1–8.0) | Medium (8.1–10.0) | Long (10.1–12.0) | Little (7–10) | Average (11–14) | Large (15–20) | Small (0.3–0.45) | Medium (0.46–0.65) | Large (0.66–0.85) | |
Jonkheer van Tets | + | + | + | ||||||
Natali | + | + | + | ||||||
Hollandische Rote | + | + | + | ||||||
Viksne | + | + | + | ||||||
Shchedraya | + | + | + | ||||||
129-21-61 | + | + | + | ||||||
261-65-19 | + | + | + | ||||||
111-19-81 | + | + | + | ||||||
271-58-24 | + | + | + |
The genotype choice of agricultural plants corresponding to the region of cultivation, including for berry crops, is largely determined on the basis of the genotypic variability analysis of cultivars with respect to complex economically valuable characteristics. In terms of these characteristics, it is clear from the table that the most superior characteristics are obtained in the 271-58-24 genotype. Moreover, ‘Jonkheer van Tets’ and 261-65-19 genotype have moderate biometric indicators for productivity.
In the course of the research, the biochemical composition (soluble solid concentration, titratable acidity and ascorbic acid and total phenolic contents) of the berries was also evaluated (Figure 3). Current results demonstrated that the climatic conditions have a significant influence on biochemical compositions. The SSC (soluble solid concentration) and TA (titratable acidity) were mostly found to be higher in optimal seasons, where the AA (ascorbic acid) and TPC (total phenolic contents) were mostly higher in drought seasons. A significant difference was noted among the cultivars/genotypes. The highest SSC content was noted in ‘Hollandische Rote’ and the lowest in ‘Shchedraya’. On the other hand, the highest TA was observed in the 111-19-81 genotype and the lowest in ‘Natali’. The high sugar content combined with the low organic acid content provides the berries with a pleasant sweet taste (‘Natali’, ‘Viksne’ and ‘Hollandische Rote’). The balance of sugar to organic acids is important for describing the flavour characteristics of the fruits (Battino and Mezzetti, 2006; Talcott, 2007). Similar results were noted by Gorbunov and Kukushkina (2019) for some red currant genotypes which had a complex hybrid origin, i.e. as a result of crossing the species forms of red currants
One of the important indicators of the nutritional value of berries is the content of ascorbic acid (Djordjević et al., 2010). The analysis of the obtained results (average for 2014–2018) showed a significant variability among the studied genotypes, which is consistent with the data obtained on this culture by other scientists (Talcott, 2007; Djordjević et al., 2010). The highest content of ascorbic acid was obtained in the selected form of 271-58-24, while ‘Jonkheer van Tets’, ‘Hollandische Rote’ and ‘Natali’ were characterised by a low index. Contrary to current results, in studies containing ‘Jonkheer van Tets’ grown in the regions of Belgium (Djordjević et al., 2010) and Turkey (Çelik and İslam, 2019), ascorbic acid content was found to be slightly higher but comparable with the data obtained in a temperate continental climate. Similar with the AA, the TPC of the fruits was found to be highest in the 271-58-24 genotype. No significant difference was noted between ‘Viksne’ and the 271-58-24 genotype. These two forms were observed to have about 2-fold of TPC than the others. The lowest content was noted in the 111-19-81 genotype.
A moderate positive correlation was found between the SSC and TA content of the berries (Figure 4A). A moderate negative correlation was observed between the SS and TA contents. A moderate-to-strong correlation was then observed between the AA and TPC of the berries, supporting the basic information that AA is a constituent of TPC of the fruits. One of the important results of the current study was about the correlation between the TPC and berry weight, which was moderately negative. Contrary, the TPC was found to have a moderately positive correlation with the raceme length and number of berries in a raceme. The highest correlation was observed between the raceme length and number of berries in a raceme. The impacts of the test traits on the cultivars/genotypes are shown in Figure 4B. Results demonstrated that ‘Shchedraya’ and ‘Natali’ are mostly characterised by their high yield, the 271-58-24 genotype by its high AA, TPC and the number of berries in a raceme, the 261-65-19 genotype, ‘Viksne’ and ‘Jonkheer van Test’ by the high raceme length, SSC, SS and TA and ‘Hollandische Rote’, 111-19-81 and 129-21-61 genotypes by high berry weight. Hierarchical clustering (Figure 4C–4D) suggested four meaningful clusters: the introduced cultivars produced one cluster, Russian cultivars are another cluster, 261-65-19, 111-19-81 and 129-21-61 genotypes make up a third cluster and the 271-58-24 genotype (superior in terms of phenolic contents) forms the fourth cluster.
The yield and quality of products are determined by the state of the water regime of plants during the growing season. Throughout the studies, there were periods with optimal weather conditions and dry ones. An important indicator of the response of plants to stressful conditions (drought) is the assessment of water balance (El-Hendawy et al., 2019). A fairly accurate method of assessing the water status is focussed on traditional physiological measurements (Kovar et al., 2019). The water content in the leaves of the studied samples was determined in years with optimal moisture and in drought periods. At the same time, the field humidity of the soil at a depth of 0–200 mm and 200–400 mm was taken into account. The correlation among the traits is described in Figure 5. Results suggested that there is a very strong negative correlation between bound water and free water of leaves in May, and this correlation decreases in July. At the same time, a strong positive correlation was observed between the coefficient of bound/free water and bound water. The bound water in leaves was negatively correlated with the soil moisture and absolute soil moisture in the top layer (0–200 mm). This correlation decreased in July and was found to be negligible in lower layers (200–400 mm). Contrary to bound water, free water had a positive correlation with the soil moisture content of the soil. Simply, it can be concluded that the increase in the soil moisture content in the upper layers can cause an increase in the free water content of the leaves and a decrease in the bound water content of the leaves. Moreover, these correlations were higher in May as compared with those in July. It was also found that the water content of leaves and transpiration have a strong positive relationship with soil moisture at a depth of 0–200 mm but a week correlation with soil moisture at a depth of 200–400 mm. Results also showed that the transpiration of the leaves decreases in later developmental stages.
According to the results obtained, the optimal soil moisture content for the growth and development of plants is considered to be at least 70%. In the conditions of the field experiment, this corresponds to 17.3% of the absolute soil moisture (Roeva and Motyleva, 2013). At the same time, the moisture reserve in the underlying soil layers (200–400 mm) is higher than that in the upper horizon. Similar results were obtained by other scientists. It is suggested that fruit plants get the necessary amount of moisture due to the growth of roots in the deeper layers of the soil. The biomass of roots located in the deep layers of the soil correlates with the content of moisture reserve in the underlying layers of the soil (
The supply of moisture to plants is determined not only by the water content in the soil but also by the ability of plants to absorb it. The quantitative moisture content in the assimilation apparatus of red currant genotypes, as well as the change in this indicator during the growing season and growing conditions, allow us to give an objective assessment of water balance of plants and assess the degree of drought resistance. The water content in the leaves reflects the complex effect of air and soil drought. In the course of the research, direct linear dependence of the level of soil horizon moisture and leaf hydration was revealed. Under optimal weather conditions, the water content in the leaves was high (on average 64.68%), and the plants absorb the required amount of moisture from the soil horizon at a depth of 0–200 mm. In drought season, the water content in the leaves decreased (to an average of 60.59%), and the plants used water for growth and development from lower layers with a thickness of 200–400 mm. The maximum reduction in leaf hydration was in ‘Shchedraya’ and in the 261-65-19 selected form.
By the time of berry maturation (July) and due to the physiological ageing of the leaf blade, the water content in the leaves of red currants decreases (Figure 6), and this phenomenon does not depend on environmental conditions (Keller et al., 2006). The studies have shown the variability of this trait during the growing season in conditions of optimal moisture. The highest values of bound water to free water were in ‘Hollandische Rote’, ‘Jonkheer van Tets’ and the 271-58-24 selected form. From May to July, there is an increase in bound water content and, at the same time, a sharp decrease in the rate of water loss. There is a decrease in the overall water content of the leaves since water loss depends on the water content of the leaves. According to the literature data, as this content decreases, the amount of water that can be evaporated from the leaf surface progressively decreases (Williams and Amer, 1957). In addition, the increase in temperature and average humidity in July compared to May is the reason for a decrease in the rate of water loss since high humidity interferes with the normal course of the transpiration process and negatively affects the movement of nutrients and water through the xylem and the regulation of temperature and the movement of the closing cells of plant stomata (Kuznetsov and Dmitrieva, 2005). The intensity of transpiration during this period decreased sharply in comparison with optimal conditions, which was associated with a decrease in the rate of nutrient and water supply to photosynthetic cells and the movement of the closing stomatal cells. In more drought-resistant forms of plants, the evaporation process was less intense than in unstable ones (Morales et al., 2013; Basu et al., 2016). The study revealed a positive correlation between the level of transpiration and soil moisture and a negative relationship between transpiration and the amount of bound water in the plant.
The results of the water regime indicators are considered as one of the important elements in the regulation of the production process and help assess the ability of the studied red currant genotypes to tolerate the stress factors of the growing season with minimal yield losses. However, ‘Hollandische Rote’, ‘Jonkheer van Tets’, ‘Shchedraya’ and the 271-58-24 selected form showed high yields consistently (9.5–20.0 t · ha−1). According to the field observations, these genotypes were characterised by a lower percentage of berry shedding. For farms, the establishment of plantations with these cultivars would allow us to get a fairly high profit and ensure the profitability of crop production in a temperate continental climate. For scientific institutions, these genotypes are of interest to attract breeding for adaptability and yield.
This study was aimed at assessing and understanding the adaptation process of introduced cultivars and breeding genotypes of red currants in temperate continental climates and regions with a similar climate. Based on the long-term study of the red currant cultivar phenotypes, it has been found that the choice of a particular cultivar for production or breeding research is determined by genotypic variability based on the analysis of economically valuable and adaptively significant traits. None of the selected genotypes was found to be resistant to any of the diseases/pests, but ‘Jonkheer van Tets’, ‘Hollandische Rote’ and 111-19-81 were less affected from these diseases/pests. The highest berry weight was observed in the 261-65-19 genotype (0.65 g), while the highest yield was noted in ‘Hollandische Rote’ (15.6 t · ha−1).
In periods of unstable hydrothermal conditions, the cultivars of foreign selection have developed and maintained a system of morphological and physiological adaptations that protect them from stress factors. These studies clearly show the dependence of the yield of the cultivar upon the state of the water regime of plants and soil moisture. The direct dependence of the water content of the leaves of the introduced red currant cultivars on the soil moisture and the soil horizon has been revealed. The nature of the correlation relationships made it possible to determine the direction of individual trait selection. The degree of drought resistance of cultivars is determined by the amount of bound water in the leaves, the rate of transpiration and the period of development. Accurate information about the period of plant ontogenesis when plants experience the greatest moisture deficiency can be taken into account in breeding programmes to increase the resistance of cultivars to drought. Indicators of the water regime of red currant cultivars can be used to predict the yield. The cultivars of European and Russian breeding such as ‘Hollandische Rote’, ‘Jonkheer van Tets’ and ‘Shchedraya’ retain their resistance to the stress factors of the growing season of the temperate continental climate. In the framework of breeding programmes aimed at finding sources and donors of valuable economic-biological and adaptive significant traits, it is necessary to use selected forms obtained on the basis of the descendant of a large-fruited subspecies