Soil water storage depletion
Root zone soil water storage is mostly responsible for the proper growth and development of plant at different phenophases. So, to obtain satisfactory plant growth the water necessary meet their needs and no periods of moisture starvation prevails. The Fig 2(a-c) shows the different soil moisture storage under different irrigation treatments; where, the peaks appeared due to the application of irrigation water and the depletion of soil moisture by plant uptake and/or evaporation caused trough in the curve. Regarding irrigation treatments, soil moisture depleted at a rate of about 2.5 and 4.3 mm d-1 during early vegetative and peak vegetative periods, respectively. I3 more drastically reduced the soil moisture storage up to pod formation period; from where it increased water storage to 84 mm due to irrigation and lastly the decreased to the least amount (62 mm) at maturity period (Fig 2c). In case of I2, the steady depletion of soil moisture occurred from pod initiation to harvest. With the dying of soil, roots sensed resistance to grow and thus decreased development of finer roots and increased metabolites deposition in roots to increase strength which ultimately cause lesser water extraction.
Hao et al., (2015) similarly experienced higher water extraction in well water treatment (50% ETc) than water stresses ones (100% and 75% ETc) in maize. It was observed that effect of P came to exist starting from peak vegetative period and proceeded afterward. P2 resulted the maximum water storage followed by P1. P induced the higher root growth implied more water extraction than lesser P application resulting less water available to the treatments
(Mukherjee et al., 2022). The effect of P was mostly observed under I1 and I2, there was no such effect of P application observed under I3. The available water content improved the plant physiology including root growth which emphasized due to the ample availability of P in the root zone soil and thus, showing good interaction; on the other hand, the lesser amount of available water presence for I3 hindered the transportation of P to the roots and from roots to other parts of the plants. There are similar findings as observed from
Sarkar et al., (2017) and
Chtouki et al., (2022).
Soil water stress coefficient
Soil water stress coefficient (Ks) emphasizes the moisture-supplying capacity of soil that depends on available soil water content, soil water depletion and available water capacity (
Nandi et al., 2023). Ks shows no water stress up to the vegetative period, thereafter stress appeared at different quantities (Fig 3a-c). I2 showed miniature stress with Ks around 0.9 at initiation of flowering but that stress intensified at pod formation and maturity period with 35 and 67% stress, respectively. While under I3, the amount of water stress was comparatively higher about 40 and 45% at flowering and pod initiation periods; although that stress reduced to 10% at the pod formation period but increased to a maximum of 55% during the maturity period denoting heavily stress affected plants. Where I1 showed the least water stress which was 5, 15 and 27% during the vegetative, pod formation and maturity period of green gram, respectively. The stress under I3 was significantly higher than I2. Regarding the effect of P on water stress modification, it was observed that P significantly modified the water stress. P2 was recorded to produce the least amount of water stress followed by P1 and the most water stress was recorded under P3 which resulted in 18% stress during the vegetative period, 35% at flowering and 18% at pod formation period; although, all the stresses at the critical phenophases under P3 were below the critical limit (<40%). The interaction between I and P was significant mainly during flowering, pod formation and maturity periods. The stress appearance under P3 was due to the plant water extraction causing a decrement in soil water storage that positively impacted on plant growth. A similar reflection was also reported by
Saha et al., (2020).
Root morphology
Root length density
Variation of root distribution is observed accompanied by soil moisture content in the root zone (Fig 4a). The effect of K was observed as non-significant and because of that only the effect of irrigation and P were shown and discussed in this section. P significantly improved root length density (RLD) and the maximum improvement was noticed under full irrigation (I1) followed by deficit irrigation (I3). The RLD variations as observed in our study among different irrigation treatments go hand in hand with the observations of
Kang et al., (2000), who reported a 14% higher decrement of RLD at severe water stress as compared to medium water deficit. The interesting observation was the interaction of P and I. Fig 4a shows that the maximum (27%) increase in RLD from P1 to P3 was observed under I2, where the increase was merely 14% in the case of I1. The improvement of roots under water deficit I2 condition was more with the supply of P.
Lukowska (2013) observed the development of long taproots because of greater water availability at lower depths. While the decrement from P1 to P2 was almost the same for both I1 and I2 irrigation treatments. On the other hand, the application of lesser P (P2) produced lesser RLD but the P1 and P3 showed no significant differences in RLD values. There are several reports describing the decrement of RLD under the deficiency of P
(Duan et al., 2021; Hadir et al., 2020). When grown under Limited phosphorus (P) availability root elongation gets inhibited and thus exhibits a shallower architecture
(Sharma et al., 2017). On the other hand,
Teng et al., (2013) reported an increase in RLD under the influence of elevated P-fertilizer rate in wheat.
Average root diameter
The average diameter (RD) denotes the dominance of finer or coarser roots under different I and P treatments in green gram (Fig 4a). The figure implies that with the decrement of irrigation frequency, RD increased, while RD decreased with the improved amount of P application. P produced finer roots under I1 and I2, although, P application showed no such significant effect of RD under I3. More number of finer roots were produced under slight water stress (I2) with the application of higher P (P3) fertilizer. A similar P’s effect under water stress was reported by
Mataa et al., (2019) while working with common beans. Plants develop short suberized roots when water stress appears as the top soil starts to dry which is the survival mechanism of plants for reducing water loss from plant roots
(Whitmore et al., 2011).
Yield and evapotranspiration
Table 2 shows the effect of I, P and K on the grain yield, evapotranspiration and water productivity of green gram. It shows that I3 produced the maximum grain yield which was 18 and 47% greater than I1 and I2. The application of P improved grain yield irrespective of irrigation management. P3 produced the maximum grain yield of 721 kg ha
-1 followed by P1. P1 and P3 improved 26 and 35% grain yield over P2 under I2 and improved 32 and 40% grain yield over P2 under I1. The application of the higher amount of P (P3) only increased by 8% grain yield under I3. Photosynthesis-driven grain yield of crops decreases with the reduction in the relative water content (RWC) of leaves. While, responses to water deficit are the reduction of transpiration and thereby reduction of photosynthesis resulting in significant consequences on grain yield (
Álvarez et al., 2011). Similarly,
Trout and DeJonge (2017) reported a decline in grain yield with a reduction in irrigation amount.
Evapotranspiration amount was varied among different I and P treatments. I1 resulted in 13% higher ET than I2; while P1 and P3 produced 9 and 14% higher ET than P2, respectively (Table 2). The implication of I1P3 recorded the highest ET of 173 mm followed by I1P1 of 158 mm. The introduction of P1 and P3 also improved 6 and 10% ET under I2. However, not so not-so-significant enhancement of ET by P was observed under I3. The improvement of ET with the improvement of RLD either by P application or supplement irrigation has previously been provided by
Kazemi et al., (2021) and is presented in Fig 5.