1. Introduction
Recent climatic fluctuations, the reduction of arable land, escalating production input costs, socio-cultural shifts, and rural-to-urban migration threaten the resilience of agricultural systems globally and in Türkiye. These dynamics undermine the ability of farming systems to sustainably meet growing food demands and pose increasingly serious risks to global food security if not promptly addressed [
1].
Animal-derived proteins are essential for balanced human nutrition. The recommended daily protein intake is approximately 70 g per person, ideally sourced equally from plant and animal origins. While plant-based protein intake in Türkiye is generally adequate, consumption of animal-based protein remains insufficient. Livestock-derived foods, especially from cattle and small ruminants, play a critical role in providing animal proteins. However, feed costs accounting for nearly 70% of total production expenses severely affect the profitability of livestock operations, leading to reduced production, higher consumer prices, and diminished access to animal-sourced proteins.
A key barrier to sustaining livestock production is the insufficient supply of high-quality roughage. In Türkiye alone, 2022 data revealed 23.846 million hectares of arable land, of which only 2.752 million hectares are devoted to forage cultivation, despite a raw roughage demand of approximately 71.28 million tons annually [
2,
3]. Thus, a significant quality and quantity gap persists in forage resources.
Although cultivation of forage crops has increased in recent years, shortfalls in quality and quantity remain persistent. Economically feasible alternatives that support ruminant digestion are therefore vital. Enhanced forage cultivation can alleviate pressure on overgrazed pastures, reduce fallow land, improve soil fertility and water retention, and foster healthier crop rotations—offering multiple ecosystem and agronomic benefits.
Forage pea (
Pisum sativum L. var.
arvense) is an annual legume forage species highly valued for its palatability, balanced nutrition, and adaptability to cool climates. It requires minimal nitrogen fertilization, contributes 5–15 kg N/da to the soil via biological fixation, and produces clean stubble conducive to subsequent crops. In Türkiye, it is cultivated across Southeastern Anatolia and coastal regions during the winter season [
4,
5]. At full flowering, its forage contains ~20% crude protein, while the seeds hold 20–30% crude protein and are rich in lysine qualities that make them suitable alternatives to soybean in European ruminant diets [
6]. Its dual role as forage and green manure underscores its agroecological importance.
Given these attributes, evaluating the vigor and performance of forage pea seed lots prior to sowing is critical. Seed lots with high laboratory germination rates may nonetheless exhibit poor field emergence due to variations in seed vigor influenced by storage conditions. Seed vigor a concept encompassing longevity, rapid germination, and robust seedling establishment under suboptimal conditions is a stronger predictor of field performance than germination alone [
7,
8]. Techniques such as germination speed index (GSI), mean germination time (MGT), and radicle emergence tests at low temperatures have proven effective in vigor assessment and in forecasting field emergence in forage species [
9,
10,
11]. Storage conditions play a pivotal role in determining seed longevity. Legume seeds, including peas, deteriorate rapidly under unfavorable moisture and temperature regimes [
7,
12]. Molecular studies show that oxidative damage, membrane degradation, and impaired DNA repair mechanisms underlie seed aging [
7,
13]. Modern research has also revealed that seed coat structure, antioxidant capacity, oligosaccharide composition, and genotype-specific traits modulate storability [
7,
14,
15].
Despite extensive research on seed longevity across crops, relatively few studies focus on forage pea vigor and field emergence under real-world storage and environmental conditions. This study aims to address this gap by evaluating vigor, field emergence, and storage resilience in forage pea seed lots using standardized laboratory assays and field trials.
2. Materials and Methods
This study was conducted during the 2021–2022 growing season under the ecological conditions of Manisa, Türkiye, specifically on the experimental fields of the Beydere Seed Certification and Testing Directorate. Complementary laboratory analyses were carried out at the laboratories of the Seed Registration and Certification Center Directorate in Ankara.
The plant material consisted of six forage pea (Pisum sativum L. var. arvense) cultivars: Uysal, Özkaynak, Kurtbey, Ürünlü, Taşkent, and Nany.
For the laboratory experiments, germination boxes, 0.9 mm-diameter washed sand, a calibrated germination chamber, sterilization equipment, an electronic moisture meter, EC meter (electrical conductivity), precision balance, potassium chloride (KCl), and standard laboratory consumables were used. Prior to experimentation, seed lots were evaluated for their physical properties. Thousand seed weights were determined, and seed moisture contents were adjusted to fall within the range of 10–14% before storage and testing.
Table 1.
Characteristics of Forage Pea Cultivars Used in the Experiment.
Table 1.
Characteristics of Forage Pea Cultivars Used in the Experiment.
| Forage Pea Cultivar |
Thousand Seed Weight (g) |
Pre-Storage Seed Moisture (%) |
Post-Storage Seed Moisture (%) |
| Uysal |
160.80 |
13.4 |
12.6 |
| Özkaynak |
141.60 |
11.4 |
13.2 |
| Taşkent |
146.40 |
11.0 |
10.6 |
| Kurtbey |
194.60 |
10.6 |
10.4 |
| Ürünlü |
123.38 |
11.6 |
13.8 |
| Nany |
118.00 |
11.7 |
10.8 |
The adjusted moisture levels ensured comparability across the cultivars in subsequent viability and vigor tests. These values were used as baseline data for evaluating the effects of storage on seed performance.
2.1. Climatic Characteristics of the Research Area
Climatic data for the experimental site (Manisa/Beydere) were obtained from the Turkish State Meteorological Service. The data, including monthly average temperatures, total precipitation, and relative humidity values, are presented in Table 2.
Table 2.
Monthly Climatic Data for the Experimental Area (Manisa/Beydere).
Table 2.
Monthly Climatic Data for the Experimental Area (Manisa/Beydere).
| Month |
Avg. Temp (°C) 2021–2022
|
Avg. Temp (°C) 1991–2022
|
Total Precip. (mm) 2021–2022
|
Total Precip. (mm) 1991–2022
|
Relative Humidity (%) 2021–2022 |
Relative Humidity (%) 1991–2022 |
| October |
18.0 |
17.8 |
50.4 |
51.8 |
67 |
64 |
| November |
12.0 |
12.1 |
86.8 |
88.9 |
76 |
73 |
| December |
8.0 |
8.1 |
135.4 |
138.2 |
81 |
80 |
| January |
7.0 |
6.6 |
127.2 |
129.0 |
82 |
79 |
| February |
7.0 |
7.9 |
105.4 |
107.7 |
77 |
75 |
| March |
10.0 |
10.5 |
77.1 |
78.4 |
73 |
70 |
| April |
15.0 |
15.1 |
53.6 |
55.5 |
68 |
65 |
| May |
20.0 |
20.3 |
38.5 |
39.3 |
59 |
57 |
| Mean |
12.0 |
12.3 |
84.3 |
86.1 |
73 |
70 |
As shown in the table, the long-term average temperature (1991–2022) in the region is 12.3 °C, while the average total precipitation is approximately 86.1 mm. The data indicate that the 2021–2022 growing season closely aligned with the long-term climatic trends, suggesting normal environmental conditions during the study period.
This climate is typical of a Mediterranean-type transitional zone, characterized by mild, rainy winters and warm, relatively dry springs—suitable for cool-season forage legumes like forage pea (Pisum sativum L. var. arvense).
These climatic data are crucial for interpreting germination, vigor, and field emergence results, as temperature and moisture are key determinants in seed metabolic activity and seedling establishment.
2.2. Plant Material and Seed Preparation
The forage pea (Pisum sativum L. var. arvense) seeds used in the study were harvested in 2021. Six cultivars Uysal, Özkaynak, Kurtbey, Ürünlü, Taşkent, and Nany—were obtained after harvest. The seeds were not subjected to any pre-treatment. Moisture content was adjusted to between 10% and 14%, and the seeds were transferred to moisture-stable paper envelopes and stored to prevent moisture fluctuations.
2.3. Experimental Design
The study was conducted in two stages:
Stage I: Initial laboratory analyses conducted without storage treatment.
Stage II: Post-storage assessments after seeds were kept for three months under room temperature and controlled storage (5 °C, 60% RH).
2.4. Laboratory Tests
2.4.1. Standard Germination Test
Conducted in accordance with [
17] rules. For each cultivar, 100 seeds per replicate were tested with four replications. Seeds were sown in 20 × 16 × 5 cm covered germination boxes containing sterilized (150 °C, 2h) 0.9 mm sand at 60% moisture. The seeds were covered with 1–2 cm of the same sand, and boxes were incubated in a germination chamber at 20 ± 1 °C. Germination speed was calculated on the fifth day, and germination percentage on the eighth day.
Picture 1.
Germination tests and seedling characteristics.
Picture 1.
Germination tests and seedling characteristics.
2.4.2. Electrical Conductivity Test
Following ISTA protocols, 50 seeds per replicate (4 reps) were weighed (precision 0.01 g), placed in 250 mL of deionized water in 500 mL Erlenmeyer flasks, and incubated at 20 °C for 24 hours. An EC meter (HI 9033), calibrated with 0.01 M KCl (1273 µS/cm at 20 °C), was used to measure electrolyte leakage. Results were expressed in µS/cm/g.
2.5. Field Emergence Test
The field trial was established on 17 November 2021 and completed on 12 May 2022, using a randomized complete block design with three replications. Each plot measured 5 m × 1.5 m (7.5 m²) with six rows and 25 cm row spacing. A total of 750 seeds were sown per plot using a precision seed drill. Sprinkler irrigation was applied immediately after sowing to ensure uniform emergence. Climatic data were recorded throughout the trial.
Picture 2.
Soaking seeds in water.
Picture 2.
Soaking seeds in water.
Picture 3.
Measurement of conductivity value.
Picture 3.
Measurement of conductivity value.
2.6. Measured Traits
Germination Speed (%): Percentage of seedlings emerged by day 5.
Germination Percentage (%): Percentage of normal seedlings by day 8.
Electrical Conductivity (µS/cm/g): Index of seed membrane integrity.
Field Emergence (%): Ratio of emerged seedlings in field plots.
Plant Height (cm): Measured from soil surface to plant apex in 10 randomly selected plants per plot.
Days to Flowering (days): Days from sowing until flowering reached a specific threshold.
Green Forage Yield (kg/da): Based on 4 m² harvested area per plot, extrapolated to per decare (da).
Dry Matter Yield (kg/da): 500 g subsample dried at 70 °C for 48 hours until constant weight, extrapolated.
Seed Moisture Content (%): Measured with an electronic seed moisture tester.
Thousand Seed Weight (g): Calculated from the mean weight of four samples of 100 seeds × 10.
Picture 4.
Field parceling, planting and field applications.
Picture 4.
Field parceling, planting and field applications.
Picture 5.
Harvesting and weighing practices.
Picture 5.
Harvesting and weighing practices.
2.7. Statistical Analysis
All data were subjected to analysis of variance (ANOVA) using the JUMP statistical software (JMP Pro 16). A factorial arrangement in a randomized complete block design was applied. Significant differences between means were determined using the LSD multiple comparison test at p < 0.05.
3. Results and Discussion
3.1. Electrial Conductivity Test Results (µs cm¯¹g¯¹)
The electrical conductivity (EC) test results indicated significant differences (p < 0.05) among forage pea cultivars and storage conditions in terms of seed vigor (
Figure 1). The mean EC values across cultivars were highest under room temperature storage conditions (38.81 µS cm⁻¹g⁻¹), followed by cold storage (35.24 µS cm⁻¹g⁻¹), and the lowest values were observed in seeds prior to storage (32.82 µS cm⁻¹g⁻¹). This trend suggests that storage conditions, particularly room temperature, can negatively affect seed membrane integrity and vigor, leading to greater electrolyte leakage.
Figure 1.
Electrical conductivity values (µS cm⁻¹g⁻¹) of forage pea cultivars measured before storage, after storage under room conditions, and after cold storage. *Different lowercase letters above the bars indicate significant differences between cultivar means according to LSD test (p < 0.05).
Figure 1.
Electrical conductivity values (µS cm⁻¹g⁻¹) of forage pea cultivars measured before storage, after storage under room conditions, and after cold storage. *Different lowercase letters above the bars indicate significant differences between cultivar means according to LSD test (p < 0.05).
Among the cultivars, Ürünlü and Uysal exhibited significantly higher EC values across storage conditions, with average values of 41.31 and 41.61 µS cm⁻¹g⁻¹, respectively, indicating reduced seed vigor. In contrast, Taşkent showed the lowest EC values in all storage conditions, with a mean of 27.90 µS cm⁻¹g⁻¹, reflecting superior membrane stability and seed quality. The interaction between cultivar and storage period was also statistically significant, emphasizing that seed response to storage is cultivar-dependent.
These findings are consistent with the principle that higher EC values are associated with greater membrane damage and lower seed vigor [
17]. Similar results have been reported by [
18], who observed elevated EC values in legume seeds stored under suboptimal conditions, leading to decreased emergence and seedling performance. In particular,
cold storage at 5°C and 60% relative humidity appeared to mitigate the increase in EC values compared to ambient room storage, highlighting its effectiveness in preserving seed quality.
3.2. Germination Rate of Forage Pea Cultivars Results
The
Figure 2. compares the germination rates (%) of six different forage pea cultivars under three storage conditions:
Before Storage,
Room Temperature Storage, and
Cold Storage.
Cold storage generally maintained the highest germination rates, indicating that low-temperature conditions are more effective in preserving seed viability.
The Taşkent cultivar showed the highest germination performance across all periods. Notably, it achieved a 92% germination rate under cold storage and was statistically grouped as “a,” indicating superiority.
The Uysal cultivar exhibited the lowest germination rates, with a significant decrease after room temperature storage. This suggests that Uysal is more sensitive to storage-related stress.
Nany and Kurtbey cultivars showed similar moderate-to-low germination rates.
Özkaynak and Ürünlü cultivars performed well with relatively high and stable germination rates across different storage periods. The LSD (Least Significant Difference) values indicate statistically significant differences among cultivars and storage periods (LSD for Period: 5.59; Cultivar: 3.95; Interaction: 2.28). The letter groupings (e.g., a, b, c...) reflect statistical significance: values sharing the same letter are not significantly different, while different letters denote significant differences. Seed germination capacity varies by cultivar, but cold storage generally yields the best results. Therefore, cold storage is recommended for long-term seed preservation. The Taşkent and Özkaynak cultivars stand out for their high and consistent germination performance.
Seed germination is a critical indicator of seed viability and vigor, and it is directly influenced by genetic factors and storage conditions. The findings of this study clearly indicate that cold storage is more effective in preserving the germination potential of forage pea (
Pisum sativum L. var. arvense) seeds compared to room temperature storage. This result aligns with previous studies suggesting that low temperatures slow down metabolic activities and reduce seed deterioration over time [
19,
20].
Among the cultivars tested, Taşkent exhibited the highest germination rates across all storage periods, particularly under cold storage conditions. This suggests a strong genetic tolerance to storage stress, making it a promising candidate for long-term seed conservation and organic agriculture systems. In contrast, the Uysal cultivar showed significantly lower germination rates, especially after room temperature storage, indicating that it is more vulnerable to unfavorable storage conditions. This cultivar may require improved seed handling practices or shorter storage durations to maintain acceptable germination levels.
Özkaynak and Ürünlü cultivars showed stable and relatively high germination across all storage conditions, demonstrating resilience that could be beneficial in various ecological settings. The statistical analysis confirmed significant differences among cultivars, storage methods, and their interactions, supporting the necessity to tailor storage protocols based on cultivar-specific responses.
Overall, this study emphasizes the importance of selecting genetically resilient cultivars and employing proper storage strategies particularly cold storage to maintain seed viability and ensure successful crop establishment.
Figure 2.
Germination rate of forage pea cultivars in different storage periods. *Different lowercase letters above the bars indicate significant differences between cultivar means according to LSD test (p < 0.05).
Figure 2.
Germination rate of forage pea cultivars in different storage periods. *Different lowercase letters above the bars indicate significant differences between cultivar means according to LSD test (p < 0.05).
3.3. Germination Power (%) Results
The
Figure 3. illustrates the germination power of six forage pea varieties under three storage conditions. Notable differences were observed between storage methods and among varieties. The cold storage condition generally maintained higher germination rates compared to room temperature.
Storage conditions had a significant effect on the germination power of forage pea seeds. In general, seeds stored in cold conditions preserved their viability better than those stored at room temperature. This result aligns with previous studies that emphasized the importance of low temperatures in reducing seed deterioration during storage.
Among the varieties, 'Taşkent' and 'Nany' showed the highest germination rates across all storage conditions, indicating superior seed longevity and potential adaptability to different storage environments. Conversely, 'Uysal' exhibited the lowest germination values, especially after room temperature storage, suggesting that it may be more sensitive to unfavorable storage conditions.
The observed variety × storage interaction was statistically significant, implying that each variety responded differently to the storage treatments. These findings suggest that both genotype and storage environment should be considered in seed conservation and storage planning.
In practical terms, cold storage is recommended to maintain seed quality in forage peas, especially for varieties with lower innate storage resilience. Selecting varieties like 'Taşkent' or 'Nany' may further enhance seed viability over time.
Storage temperature significantly affected the germination power of forage pea (Pisum sativum L. var. arvense) seeds. In this study, cold storage preserved seed viability more effectively than room temperature conditions. These results are consistent with findings from Basra et al. (2003) and Bewley et al. (2013), who reported that low-temperature environments help reduce the metabolic activity and oxidative stress that cause seed deterioration during storage.
Varietal differences were also prominent. ‘Taşkent’ and ‘Nany’ maintained high germination rates across all storage conditions, indicating superior seed quality and storage stability. On the other hand, ‘Uysal’ was more sensitive to storage conditions, especially under room temperature, exhibiting a significant decline in viability. Similar genotype-dependent responses to storage have been reported by [
21] and [
22], who emphasized the influence of genetic makeup on seed longevity.
The significant variety × storage interaction observed in this study suggests that not all varieties respond similarly to storage environments. This underlines the importance of selecting suitable genotypes for long-term seed storage programs, especially under suboptimal conditions. As proposed by [
23], seed storage potential is largely influenced by both inherent physiological properties and external storage conditions.
Comparable results have also been reported in similar studies. For example, [
24] observed germination rates ranging between 89.6% and 98.6% in forage pea seeds of different colors. [
25] found that zinc applications increased germination power to between 87% and 97.3%, while boron applications resulted in germination values ranging from 80% to 95.3%. Likewise, [
26] reported that under salt stress conditions, germination power in forage pea seeds varied between 34.5% and 98.5%. In another study, [
27] reported germination values between 89% and 95% in soybean seeds treated with different boron concentrations. These findings suggest that the germination power values observed in our study are largely consistent with those reported in the literature, and no significant deviations were found.
Overall, cold storage is recommended to maintain seed viability in forage pea, particularly for varieties like ‘Uysal’ with lower innate storage resilience. For seed producers and breeders, selecting storage-tolerant varieties such as ‘Taşkent’ may provide better outcomes in terms of germination and vigor preservation.
Figure 3.
Germination power (%) of forage pea varieties at different storage periods (Before storage, Room temperature, Cold storage). *Different letters indicate statistically significant differences (p < 0.05) according to LSD test.
Figure 3.
Germination power (%) of forage pea varieties at different storage periods (Before storage, Room temperature, Cold storage). *Different letters indicate statistically significant differences (p < 0.05) according to LSD test.
3.4. Field Emergence Rates (%) Results
Figure 4 illustrates the field emergence percentages of six forage pea (
Pisum sativum L.) varieties under two different storage conditions: room temperature and cold storage. Additionally, the average emergence values across both storage types are presented. The statistical groupings indicated by letters above the bars reveal significant differences among the varieties and treatments (LSD,
p < 0.05).
Figure 4.
Field Emergence Rates (%) of Forage Pea Varieties under Different Storage Conditions. *Different lowercase letters above the bars indicate significant differences between cultivar means according to LSD test (p < 0.05).
Figure 4.
Field Emergence Rates (%) of Forage Pea Varieties under Different Storage Conditions. *Different lowercase letters above the bars indicate significant differences between cultivar means according to LSD test (p < 0.05).
The highest field emergence rate under cold storage conditions was observed in the 'Nany' variety (88%), which was significantly superior and labeled as group "a." Under room temperature storage, 'Nany' again performed well (78%), while 'Uysal' had the lowest emergence rate (43%) and was statistically grouped as "ı." Cold storage consistently improved emergence across all varieties, with average values increasing from 64.5% (room storage) to 77.3% (cold storage).
The results clearly indicate that cold storage significantly enhances seed field emergence compared to room temperature storage. This aligns with previous findings that suggest cool, controlled storage environments help maintain seed viability and reduce metabolic deterioration [
28,
29].
Among the evaluated varieties, 'Nany' and 'Taşkent' showed the most consistent and high emergence rates, suggesting their greater tolerance to post-harvest storage conditions. Conversely, 'Uysal' and 'Kurtbey' displayed lower emergence performance, particularly under room conditions, indicating their sensitivity to storage-induced viability loss.
The interaction effect (Variety × Storage Condition) was also significant (LSD = 2.02), showing that some varieties respond more strongly to storage treatments than others. This finding underscores the importance of selecting both storage strategies and variety types carefully in seed production systems.
These results are particularly relevant for forage pea production in regions with limited cold storage infrastructure, as they highlight the need to prioritize varieties like 'Nany' that retain higher viability even when stored under suboptimal conditions.
4. Agronomic Evaluation of Forage Pea Varieties Under Different Storage Conditions
The following Table presents a comparative analysis of forage pea varieties grown under two storage conditions (room temperature and cold storage). Key agronomic traits including plant height, flowering time, green forage yield, and dry forage yield are presented along with averages and statistical information. The present study demonstrated that seed storage conditions significantly influenced plant growth and forage yield traits in Narbon vetch (Vicia narbonensis L.). Notably, cold storage conditions resulted in increased plant height, earlier flowering, and improved forage yields compared to room temperature storage, aligning with previous findings on legume crops.
4.1. Plant Height
The plant height of the Narbon vetch varieties significantly varied under both room and cold storage conditions. Among all varieties, 'Özkaynak' recorded the greatest average plant height (113.8 cm), followed by 'Taşkent' (107.2 cm), whereas 'Kurtbey' exhibited the shortest plants (90 cm). Overall, cold storage slightly improved plant height compared to room conditions. According to LSD values, differences among varieties were statistically significant (LSD (Variety) = 2.53 cm) and also influenced by storage conditions (LSD (VxS) = 1.84 cm). The coefficient of variation (CV) was relatively low (1.39%), indicating high data reliability.
4.2. Days to Flowering
The flowering time varied considerably among varieties. 'Nany' took the longest to flower (average 145.66 days), while 'Kurtbey' was the earliest maturing variety (121.33 days). Interestingly, cold storage slightly reduced the days to flowering in most varieties, indicating that it might enhance earliness. However, the LSD values showed that the variety and storage interaction (VxS) was not significant, indicating a uniform response across environments.
4.3. Green Forage Yield
Green forage yield ranged from 1105.8 kg/da ('Taşkent' under room conditions) to 1591.1 kg/da (also 'Taşkent' under cold conditions), suggesting a strong varietal response to cold storage. 'Ürünlü' showed the highest average green forage yield (1400.3 kg/da), whereas 'Kurtbey' had the lowest (1303.3 kg/da). The average yield increased notably under cold storage (1493.3 kg/da) compared to room conditions (1189.6 kg/da), highlighting the positive effect of cold storage on fresh biomass accumulation. These differences among storage conditions were statistically significant, while varietal differences were not significant for green forage yield.
4.4. Dry Forage Yield
Dry forage yield followed a similar trend to green forage. The highest dry yield was recorded in 'Ürünlü' (312.4–411.0 kg/da), followed by 'Nany' and 'Uysal'. As with green yield, cold storage enhanced dry matter accumulation in all varieties. The average dry yield under cold conditions (415.4 kg/da) was significantly higher than under room storage (297.9 kg/da). Again, the differences among varieties were not statistically significant, as indicated by the LSD values.
The results indicate that cold storage has a generally positive effect on plant height, green and dry forage yield, and slightly accelerates flowering in Narbon vetch varieties. Although varietal differences in yield were not statistically significant, consistent trends suggest that 'Ürünlü', 'Taşkent', and 'Nany' may be more suitable for high biomass production under improved seed storage conditions.
The shorter flowering duration observed under cold storage implies potential benefits in escaping terminal drought stress, especially in regions with shorter growing seasons. The varieties 'Kurtbey' and 'Ürünlü', being early maturing, could be useful in such environments. On the other hand, the tall and high-yielding varieties like 'Özkaynak' and 'Taşkent' may be better suited for areas with longer vegetative periods.
Overall, cold storage appears to improve early vigor and biomass productivity, possibly by preserving seed viability and physiological quality. This study highlights the importance of seed storage conditions on field performance and suggests that selection of appropriate varieties combined with optimized storage methods can enhance forage production efficiency.
4.5. Effect of Storage Conditions on Plant Height and Flowering
The significantly taller plants observed under cold storage (average 103.53 cm) compared to room conditions (101.36 cm) suggest that
seed vigor was better maintained, resulting in improved early growth and biomass accumulation. These findings are consistent with the work of [
30], who reported that optimal seed storage conditions preserve enzymatic activity and hormonal balance, supporting better seedling establishment and vegetative development in legumes.
Additionally, cold storage led to slightly
earlier flowering across most varieties, with the average days to flowering reduced from 134.00 days (room) to 131.33 days (cold). [
31] found that lower storage temperatures contributed to improved germination and uniform seedling emergence, which often correlates with earlier phenological development. Early flowering is agronomically advantageous, especially in Mediterranean climates, as it allows crops to escape terminal drought stress [
32].
4.6. Forage Yield Performance
Both green and dry forage yields were higher under cold storage, with an average green yield of 1493.3 kg/da and dry yield of 415.4 kg/da, compared to 1189.6 kg/da and 297.9 kg/da, respectively, in room-stored seeds. The variety 'Ürünlü' consistently performed well in both green and dry forage production, suggesting genetic potential combined with enhanced seed physiological quality.
These results are supported by [
33], who highlighted the critical role of seed quality in determining field emergence and biomass yield in forage legumes. Similarly, [
34] reported that higher seedling vigor, achieved through cold storage, leads to better canopy development and forage accumulation.
While the differences among varieties for forage yield were not statistically significant, the
overall trend showed that some varieties ('Ürünlü', 'Taşkent', 'Nany') responded more positively to cold storage, indicating a
variety-dependent response to storage conditions. [
35] emphasized the importance of considering genotype × environment interactions, particularly in studies involving seed handling and crop performance.
4.7. Implications for Agronomic Practice
These findings suggest that cold storage of Narbon vetch seeds can significantly enhance forage productivity and phenological development, especially under organic or low-input systems where seedling vigor is crucial. The results underline the importance of maintaining high seed quality through appropriate post-harvest handling and storage protocols.
Furthermore, the selection of early-flowering and high-biomass varieties like 'Ürünlü' and 'Taşkent' could provide adaptive advantages in semi-arid and Mediterranean environments, aligning with the conclusions of [
36] who emphasized the value of early maturity and forage potential in vetch breeding programs.
Formun Üstü
Formun Altı
Table 3.
Agronomic Traits of Forage Pea Varieties under Different Storage Conditions.
Table 3.
Agronomic Traits of Forage Pea Varieties under Different Storage Conditions.
Varieties
|
Plant Height
|
Flowering Time
|
Green Forage
|
Dry Forage
|
| Room (cm) |
Cold (cm) |
Avg. |
Room (days) |
Cold (days) |
Avg. |
Room (kg/da) |
Cold (kg/da) |
Avg. |
Room (kg/da) |
Cold (kg/da) |
Avg. |
| Nany |
100 f |
104 cd |
102 c |
146.33 a |
145 |
145.66 a |
1186.2 |
1524.4 |
1355.3 |
306.5 |
429.5 |
368.0 |
| Özkaynak |
113 a |
114.6 a |
113.8 a |
138.33 b |
136.33 |
137.33 b |
1159.1 |
1488.9 |
1323.9 |
296.4 |
405.7 |
351.0 |
| Uysal |
101.2 ef |
103 de |
102.2 c |
136 c |
132 |
134.00 c |
1252.9 |
1382.2 |
1317.5 |
306.5 |
401.1 |
353.8 |
| Taşkent |
106.3 bc |
108 b |
107.2 b |
134 c |
131 |
132.50 d |
1105.8 |
1591.1 |
1348.4 |
279.8 |
441.5 |
360.6 |
| Ürünlü |
100 f |
101.6 def |
100.8 c |
127 d |
123.33 |
125.16 e |
1276.2 |
1524.4 |
1400.3 |
312.4 |
411.0 |
361.7 |
| Kurtbey |
88 h |
92 g |
90 d |
122.0 e |
120.33 |
121.33 f |
1157.8 |
1448.9 |
1303.3 |
286.1 |
403.6 |
344.8 |
| Average |
101.36 b |
103.53 a |
|
134.00 a |
131.33 b |
|
1189.6 b |
1493.3 a |
|
297.9 b |
415.4 a |
|
|
LSD(Variety)
|
2.53 |
3.35 |
Not Sig. |
Not Sig. |
|
LSD(VxS)
|
1.84 |
Not Sig. |
Not Sig. |
Not Sig. |
|
CV(%)
|
1.39 |
0.81 |
12.61 |
10.60 |
5. Conclusions
This study demonstrated that storage conditions have a significant impact on the seed quality and agronomic performance of forage pea (Pisum sativum L. var. arvense) cultivars. Cold storage at 5 °C and 60% relative humidity effectively preserved seed vigor, as evidenced by lower electrical conductivity values, higher germination rates, and improved field emergence compared to room temperature storage. Among the cultivars tested, Taşkent, Nany, and Özkaynak showed superior seed viability and vigor across all storage periods, while Uysal and Kurtbey were more vulnerable to deterioration, particularly under ambient conditions.
The positive influence of cold storage extended to field performance, resulting in taller plants, earlier flowering, and higher green and dry forage yields. Notably, Ürünlü and Taşkent cultivars produced the highest biomass yields under cold storage, highlighting their potential for high productivity when optimal seed handling practices are employed.
The significant interactions between cultivar and storage conditions underscore the importance of considering genotype-specific responses when developing seed storage strategies. These findings emphasize that maintaining seed quality through appropriate post-harvest storage practices—particularly cold storage—is essential for ensuring successful crop establishment, maximizing forage yield, and supporting sustainable agricultural production in Mediterranean and similar agro-ecological zones.
Future studies may focus on the long-term effects of different storage durations and the integration of biochemical and molecular indicators to further elucidate the mechanisms behind varietal differences in seed longevity and field performance.
Author Contributions
This research is S.A 's master thesis work. S.K.A. also served as a consultant in this research. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
The data presented in this study are available within the article.
Acknowledgments
This study was the article based on the master's thesis coded FBE EYK 2023/822692 for the Department of Field Crops, Institute of Sciences, Bilecik Seyh Edebali University.
Conflicts of Interest
The authors declare no conflicts of interest.
References
- Gülümser, E., Mut, H., Başaran, U., & Çopur Doğrusöz, M. Determination of the quality characteristics of silages obtained by mixing pea and oat at different ratios. Journal of the Institute of Science and Technology 2021, 11, 763–770. [CrossRef]
- TURKSTAT. Crop Production Statistics. Turkish Statistical Institute (TURKSTAT): Ankara, Türkiye, 2023. Available online: https://data.tuik.gov.tr/Kategori/GetKategori?p=Tarim-111 (accessed on 12 April 2023).
- TAGEM. Forage Crop Production, Current Status and Measures to Be Taken within the Scope of Climate Change – Workshop Final Report; General Directorate of Agricultural Research and Policies (TAGEM): Ankara, Türkiye, 2023; pp. 9–10. [Google Scholar]
- Açıkgöz, E., vd. (1985). Mineral elementsand amino acid concentrations in field pea and common vetch herbage sand seeds. J. Agronomy and Crop Sci., 55: 179-185.
- McKenzie, D.B. and D. Sponer. (1999). White Lupin: An alternativetopea in oatlegumeforagemixturesgrown in newfoundland. Can. J. PlantSci., 79: 43-47.
- Manga, İ.; Acar, Z.; Ayan, İ. Legume Forage Crops; Lecture Notes No: 274, Faculty of Agriculture, Ondokuz Mayıs University: Samsun, Türkiye, 1995. [Google Scholar]
- Reed, V. , Finch, B., Souza, J., Watkins, P., & Arnall, B. (2022). Soil sampling depth impact on phosphorus yield response prediction in winter wheat. Agricultural & Environmental Letters, 7(1), e20067. [CrossRef]
- Finch-Savage, W. E. , & Bassel, G. W. (2016). Seed vigour and crop establishment: extending performance beyond adaptation. Journal of Experimental Botany. [CrossRef]
- Lv, Y., Zhang, S., Wang, J., & Hu, Y. (2016). Quantitative proteomic analysis of wheat seeds during artificial ageing and priming using isobaric tandem mass tag labeling. PLoS ONE, 11, e0162851. [CrossRef]
- Powell, A. A. (2022). Aerated hydration treatment for seed invigoration: mechanisms and applications. In Seed Improvement by Selection and Invigoration (pp. 126–133). Piracicaba: Sci. Agric.
- Tao, Q. , Chen, D. ( 203, 116–126. [CrossRef]
- Ellis, R. H. , & Roberts, E. H. (1980). Improved equations for the prediction of seed longevity. H. ( 45(1), 13–30. [CrossRef]
- Wiebach, J. , Nagel, M., Börner, A., Altmann, T., & Riewe, D. Age-dependent loss of seed viability is associated with increased lipid oxidation and hydrolysis. Plant, Cell & Environment 2020, 43, 303–314. [Google Scholar]
- Zinsmeister, J., Leprince, O., & Buitink, J. (2020). Molecular and environmental factors regulating seed longevity. Biochemical Journal, 477(2), 305–323. https://doi.org/10.1042/BCJ20190165
researchgate.net+3pubmed.ncbi.nlm.nih.gov+3pmc.ncbi.nlm.nih.gov+3.
- Chen, S.-C. , Wu, L.-M., Wang, B., & Dickie, J. B. Macroevolutionary patterns in seed component mass and different evolutionary trajectories across seed desiccation responses. New Phytologist 2020, 228, 770–777. [Google Scholar] [CrossRef] [PubMed]
- Turkish State Meteorological Service (TSMS), 2023.
-
ISTA (International Seed Testing Association). (2022). International Rules for Seed Testing. Bassersdorf, Switzerland: ISTA.
- Zhang, H. Liu, Y., Yang, J., Wang, Y., & Du, Y. Effects of storage conditions on seed vigor and membrane permeability in legume species. Seed Science and Technology 2021, 49, 215–227. [Google Scholar] [CrossRef]
- Bewley, J.D.; Bradford, K.J.; Hilhorst, H.W.M.; Nonogaki, H. Seeds: Physiology of Development, Germination and Dormancy, 3rd ed.; Springer: New York, NY, USA, 2013. [Google Scholar]
- Copeland, L.O. , & McDonald, M.B. (2001). Principles of Seed Science and Technology (4th ed.). Springer Science+Business Media.
- Demir, İ.; Ellis, R.H. Changes in seed quality during seed development and maturation in tomato. Seed Sci. Res. 1992, 2, 81–87. [Google Scholar] [CrossRef]
- Cicek, N.; Tilki, F. Effects of storage temperature and duration on seed germination of Ulmus glabra Huds. Seed Sci. Technol. 2007, 35, 524–528. [Google Scholar]
- Ellis, R.H.; Roberts, E.H. Improved equations for the prediction of seed longevity. Ann. Bot. 1980, 45, 13–30. [Google Scholar] [CrossRef]
- Avcı, S.; Doğan, M.; Kahrıman, F. Bazı yem bezelyesi çeşitlerinde farklı tohum renklerinin çimlenme özelliklerine etkisi. Turk. J. Agric. Nat. Sci. 2020, 7, 67. [Google Scholar]
- Mokhtari, N.; Kızılgeçi, F. Yem bezelyesinde çinko ve bor uygulamalarının çimlenme ve fide gelişimi üzerine etkileri. Çukurova J. Agric. Food Sci. 2022, 37, 99–110. [Google Scholar]
- Demirkol, G.; Albayrak, S.; Kocaman, E. Tuz stresinin yem bezelyesi (Pisum sativum ssp. arvense) çimlenmesi ve gelişimi üzerine etkileri. Int. Anatolia Acad. Online J. Agric. Sci. 2019, 7, 354–359. [Google Scholar]
- Mokhtari, N.; Kızılgeçi, F. Bor uygulamalarının soya fasulyesinde çimlenme ve fide gelişimi üzerine etkisi. Mehmet Akif Ersoy Univ. J. Inst. Sci. Technol. 2021, 12, 28–30. [Google Scholar]
- Smith, R.; Jones, T. The effects of storage temperature on seed viability and vigor. J. Seed Sci. 2017, 39, 123–130. [Google Scholar] [CrossRef]
- Kaya, M.D.; İpek, A.; Öztürk, A. Influence of seed storage conditions on germination and emergence in leguminous crops. Turk. J. Agric. For. 2020, 44, 312–320. [Google Scholar] [CrossRef]
- Hacisalihoglu, G.; Armstrong, P.R.; Settles, A.M. Prediction of germination and seed vigor using machine learning and near-infrared spectroscopy. Seed Sci. Technol. 2010, 38, 60–72. [Google Scholar]
- Basbag, M.; Aydin, A.; Güler, M. The effect of different storage conditions on seed quality in legume species. J. Food Agric. Environ. 2009, 7, 460–463. [Google Scholar]
- Maqbool, M.M.; Shahid, M.; Sarwar, N. Yield and phenological response of vetch genotypes under rainfed conditions. Pak. J. Agric. Sci. 2015, 52, 899–904. [Google Scholar]
- Açıkgöz, E.; Akbaş, M.E.; Mert, M. Effect of seed quality on field emergence and forage yield in vetch cultivars. Turk. J. Agric. For. 2003, 27, 23–28. [Google Scholar]
- Kayisoglu, B.; Sade, B. Influence of seed storage conditions on forage quality and yield of common vetch (Vicia sativa L.). Legume Res. 2015, 38, 641–647. [Google Scholar]
- Sade, B.; Kaya, B.; Onal-Ascioglu, R. Genotype × environment interaction for yield and quality traits in vetch (Vicia spp.) under different agro-ecological conditions. Euphytica 2016, 210, 135–145. [Google Scholar]
- Acar, Z.; Ayan, I.; Mut, H. The importance of vetch species for sustainable forage production in dry areas. J. Agric. Sci. 2018, 24, 365–374. [Google Scholar]
|
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2025 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).