Number of reproductive stems
The results indicated a significant effect of irrigation treatment on the number of reproductive stems in alfalfa. In contrast, the results remained consistent across harvest treatments, as shown in Table 2. The lowest average number of stems was observed in treatment I4 (7.4 stems plant
-1), while the highest average was recorded in treatment I1 (12.2 stems plant
-1). The superiority of treatment I1 is due to soil water availability with the plant’s critical growth stages, Irrigation was applied at start of flowering and full formation of green pods, creating optimal conditions for stem formation. This process enhanced reproductive growth by promoting the production of growth hormones, which supports the formation of new stems.
Puppo et al. (2024) indicated that irrigation during the flowering stage increases the efficiency of photosynthesis and nutrient distribution. The fixed weekly irrigation (I4) does not meet the plant’s needs in the critical stages, which leads to loss water in stages when the plants do not need a lot of water. The study by
Orloff et al. (2005) showed that Alfalfa productivity can be reduced by up to 30% due to poor irrigation. There is no significant effect of harvest treatments on the reproductive stem number, as concluded from (Table 2). Harvest date has a weaker effect than irrigation, Due to the efficiency of the scheduling irrigation making the harvest date less influential on the stem number.
Mature racemes per stem
The number of mature racemes was significantly affected by irrigation, harvesting treatments and their interaction, as presented in Table 3. The results demonstrate a clear and significant superiority of treatment I1, which produced the highest average number of racemes (13.2 racemes stem
-1). Additionally, the table reveals that H2 (12.5 raceme stem
-1) significantly outperformed the other harvest treatments.
The significant superiority of treatment I1 can be attributed to the precise synchronization of irrigation with flowering stage, which increased the number of buds. This aligns with the findings of
Jia et al. (2024), who linked improved pollination efficiency to optimal soil water availability. The I1 treatment involved synchronizing irrigation with the physiological growth stages. This alignment was particularly evident in H2, where irrigation supported raceme growth completion before abscission began. The small number of mature racemes in the I4 treatment results from fixed weekly irrigation schedule fails to synchronize water supply with critical growth stages, particularly flowering, further limiting raceme development, leading to significant bud abscission. The results in the table demonstrate the significant superiority of treatment H2. This suggests that the optimal time for harvesting is after peak raceme maturity, once pollination is complete and pod formation has begun, thereby minimizing the risk of pod drop. This was evident in a significant 19% increase in the number of racemes compared to H1. Harvesting too early (H1) may result in problems like underdeveloped crops and lower yields than expected. Early harvest (bud formation) maximizes protein content but sacrifices dry matter yield, whereas later harvests (seed maturation) optimize biomass at the cost of feed quality (
Karayilanli and Ayhan, 2016). Data in Table 3 show that irrigation synchronized with growth stage (I1) enhances mature raceme count by 40% over traditional methods. Harvesting ten days after irrigation at 100% green pods results in the highest reproductive efficiency, with 15.6 raceme stem
-1.
Number of pods per raceme
Table 4 shows a significant effect of irrigation treatment on the number of pods per raceme in alfalfa. Treatment I1 produced the highest average (10.7 pods raceme
-1), with a peak at H2 (12.6 pods raceme
-1), demonstrating significant superiority. This was likely due to well-timed irrigation during critical growth stages, specifically at 25% of flowering and 100% green pods formation, which created optimal conditions for pod formation.
Jia et al. (2024) demonstrated that irrigation during flowering stage enhances pod formation efficiency, as soil water availability at critical growth stages improves photosynthesis, thereby increasing pod yield. Treatment I4 yielded the lowest number of pods (8.0 pods raceme
-1), due to its incompatibility with alfalfa’s growth stages. The fixed weekly irrigation schedule did not match the plant’s water requirements, causing stress and inefficient water use during less critical stages. Drought is the most limiting factor that reduces agricultural production in arid and semiarid regions of the world which cover more than 40% of global land (
Al-Hussaini and Alsaadawi, 2013).
Orloff et al. (2005) found that unregulated irrigation leads to a pod productivity decline of up to 35%. Treatment I3 showed a slight improvement over H1 (10.1 pods raceme
-1), because delayed last irrigation (at 25% brown pods) may have caused partial drying before full pod formation. The I2 treatment yielded satisfactory results (10.0 pods raceme
-1), though lower than I1. This difference may be attributed to the delayed second irrigation (at 10% flowering), which reduced its effectiveness in promoting pod formation compared to I1. Table 4 results show a significant effect of harvest treatments, with H2 performing best due to optimal maturity. Ten days after the last irrigation (H2) allowed complete pod formation without drought stress (as in H3) or premature harvest (as in H1). These findings align with
Yang et al. (2019), who reported that harvesting after 10-12 days maximizes pod and seed yields. Values at H1 were lower because premature harvesting prevented complete pod formation, resulting in fewer pods.
Table (4) reveals no significant differences in most interaction coefficients (
e.g., H1 and H3 in I3). The results also demonstrate stability in I4 across different harvest coefficients, due to the limited impact of traditional irrigation. The inefficiency of traditional irrigation reduces the influence of harvest date on pod numbers, suggesting that irrigation has a stronger effect than harvest timing in determining pod production. The results indicate that combining I1 with H2 approach maximizes pod and seed yield. Conversely, traditional irrigation (I4) should be avoided due to its inefficiency, as it wastes water and reduces productivity.
Seed count per pod
The results in Table 5 show that irrigation treatment significantly affected the average number of seeds per pod in alfalfa. Treatment I1 yielded the highest average (4.6 seeds pod
-1), while I4 produced the lowest (3.0 seeds pod
-1). As shown in Table 5, treatment I1 outperformed others due to its synchronization with growth stages. Applying irrigation at 25% flowering and 100% green pods ensured ideal seed formation conditions. Adequate moisture during flowering improves pollination, increasing seeds. Treatment I4 had a low seed count, since fixed weekly irrigation did not provide adequate water for optimal seed formation.
Miao et al. (2025) observed that a lack of water during seed formation reduces seed number by as much as 40%. In the I3 treatment, the last irrigation at 25% brown pods did not provide optimal moisture conditions during critical seed formation stages, potentially hindering complete seed development. I2 yielded satisfactory results (4.2 seeds pod
-1) but performed slightly worse than I1, likely because the second irrigation was delayed (10% flowering), possibly affecting seed formation efficiency.
A thousand seeds’ weight
Table 6 shows that seed weight remained stable across different irrigation treatments (I1-I4), due to strong genetic control, as seed weight is a consistent genetic property with limited influence from environmental factors such as irrigation
(Renzi et al., 2011). Additionally, the plant adapts to stress by adjusting physiological mechanisms, including nutrient redistribution, thereby maintaining stable seed weight despite varying irrigation conditions. Regarding harvest dates, harvesting treatments had a significant effect, difference between the highest (H3: 2.6 g) and lowest (H1: 2.4 g) values. Seed weight increased slightly at H3 due to complete physiological maturity, as delayed harvesting allows for full nutrient accumulation in the seeds.
Katanski et al. (2020) observed a similar trend, reporting a 5-7% increase in seed weight when harvesting was postponed until full maturity. In contrast, decrease at H1 resulted from incomplete seed formation, as early harvesting may disrupt nutrient deposition.
Seed yield
Table 7 indicates that irrigation and harvesting treatments significantly influenced the seed yield of plants. Among the irrigation treatments, I1 yielded the highest productivity (465.3 kg ha
-1), whereas I4 resulted in the lowest (348.2 kg ha
-1). Seed yield varied significantly among harvest treatments, demonstrating its sensitivity to harvest date. The highest mean yield was observed in H2 (431.1 kg ha
-1), while H1 recorded the lowest (379.6 kg ha
-1). The H2 treatment is optimal for complete seed formation with nutrients while minimizing mature seed loss. The H1 treatment significantly reduced seed yield due to fewer seeds per pod (3.7 seed pod
-1) and lower seed weight (2.4 g per one thousand seeds).
The results in Table 7 confirm a significant interaction effect between irrigation and harvesting treatments. Specifically, the I1 treatment at H2 achieved a seed yield of 538.3 kg ha
-1, the highest among other treatments. This can be attributed to the synchronization of irrigation intervals with critical growth stages, which promoted flowering and green pod formation. Consequently, seed formation improved, alongside increased seed size and weight. These factors collectively enhanced water use efficiency.
Jia et al. (2024) found that optimal irrigation practices can improve water use efficiency by 35%. The positive interaction between I1 and H2 treatments ensures complete maturation while preventing seed loss. However, the lower seed yield observed in I4, particularly with H1 (312.4 kg ha
-1), Fixed weekly irrigation fails to meet the plant’s water requirements during critical stages like flowering and seed formation, leading to significant seed loss. Additionally, early harvesting (H1) disrupts the full maturation cycle. These findings align with
Miao et al. (2025), who reported that unscheduled irrigation reduces productivity by 40-45%.
Biological yield
As shown in Table 8, both irrigation and harvesting treatments, as well as their interaction, had a significant effect on biological yield. The highest biological yield was recorded in treatment I4 (5391 kg ha
-1), whereas the lowest was observed in I1 (4925 kg ha
-1). Among the other treatments, H3 achieved the highest overall average (5306 kg ha
-1), while H1 was the least productive (4759 kg ha
-1).
Results in Table (8) show that I4 performed best in biological yield. This discrepancy can be attributed to factors such as excessive vegetative growth, delayed maturity and low biomass to seed conversion efficiency. Frequent weekly irrigation I4 promotes vegetative growth over reproductive formation, boosting biomass but reducing seed yield.
Soufan et al. (2019) found that excessive irrigation delays reproductive maturity, extending the vegetative stage. The findings indicate that treatment I1 struck an optimal balance in performance, sustaining a robust biological yield alongside an elevated seed yield (465.3 kg ha
-1). By emphasizing reproductive stage support, I1 achieved high conversion efficiency and an equilibrium between vegetative and reproductive growth.
The results of the harvest treatments presented in Table 8 confirm the significant superiority of H3, as delayed harvest allowed for complete dry matter accumulation, increased leaf area and enhanced metabolic processes. However, despite the increase in biomass, feed quality declined with harvest delay. Early harvest (H1) also presented challenges, such as insufficient carbohydrate accumulation, as this treatment interrupted the growth cycle before completion.
Harvest index
The results in Table (9) show that treatment I1 significantly outperformed the others, achieving the highest harvest index (9.47%). In contrast, treatment I4 had the lowest performance, with a harvest index of only 6.46%. Additionally, harvest timing significantly influenced the results, with treatment H2 (8.87%) demonstrating clear superiority over the other dates. According to the data in (Table 9), the I1 treatment demonstrated significantly better results. This can be attributed to the effective synchronization of irrigation with critical growth stages (
e.g., 25% flowering), which enhanced the allocation of carbohydrates toward reproductive organs
(Puppo et al., 2024). Additionally, this synchronization helped minimize excessive vegetative growth losses. The application of harvest treatment H2 to treatment I1 resulted in an 11.14% rate of complete seed formation while effectively minimizing seed loss. The lower yield index in treatment I4 resulted from excessive vegetative growth.
According to the data in (Table 9), treatment H2 demonstrated significant superiority due to its ideal harvest date, which balanced complete nutrient accumulation in the seeds while avoiding seed loss. As a result, the harvest index increased by 22% compared to H1. In contrast, early harvest (H1) led to insufficient carbohydrate accumulation and incomplete seed maturation.
The results in Table 9 demonstrate that irrigation (I1) synchronized with growth stage enhances biomass to seed conversion efficiency by 46% compared to traditional irrigation. Among harvest treatments, H2 yielded the highest harvest index due to optimal biological balance. In contrast, traditional irrigation (I4) resulted in a 35% resource loss in nonproductive plant parts.