Physiological response of Rosa damascena under drought stress
Relative water content (RWC) declined significantly with increasing drought stress, decreasing from 87.30-90.95% under 100% field capacity (FC) to 70.10-80.70% at 75% FC and 59.25-70.10% at 50% FC (Fig 1). Foliar application of potassium silicate significantly improved RWC under all irrigation regimes, with 150 mg L
-1 recording the highest values. Under 75% FC, RWC increased from 70.10% in control to 80.70%, while under 50% FC it increased from 59.25% to 69.60%. Increasing the concentration beyond 150 mg L
-1 did not provide further improvement. The reduction in RWC under drought stress is attributed to restricted water uptake and impaired cellular hydration, whereas potassium silicate improved plant water status by reducing transpiration through silica deposition on the leaf surface
(Farooq et al., 2009; Liang et al., 2007; Ashraf et al., 2025). Similar improvements in RWC following silicon application under drought stress have been reported in rose by
Al-Yasi et al. (2020);
Adamipour et al., (2022); Farahani et al., (2021) and in rye by
Hattori et al., (2008).
Chlorophyll-a (Chl-a), chlorophyll-b (Chl-b) and total chlorophyll contents declined progressively with increasing drought stress (Fig 2). In untreated plants, Chl-a decreased from 1.05 mg g
-1 FW at 100% field capacity (FC) to 0.75 mg g-1 FW at 50% FC, while total chlorophyll declined from 1.40 to 1.00 mg g
-1 FW. Foliar application of potassium silicate significantly improved chlorophyll pigments under all irrigation regimes, with 150 mg L
-1 recording the highest values. Under 75% FC, total chlorophyll increased from 1.20 to 1.57 mg g
-1 FW, whereas under 50% FC it increased from 1.00 to 1.36 mg g
-1 FW. Increasing potassium silicate beyond 150 mg L
-1 did not result in further improvement. The decline in chlorophyll under drought stress is associated with chlorophyll degradation, chloroplast damage and oxidative stress, whereas potassium silicate-maintained chlorophyll integrity and photosynthetic activity by improving membrane stability and antioxidant defence
(Gupta et al., 2020; Zarif et al., 2025; Goyal et al., 2025; Liang et al., 2007). Similar beneficial effects of silicon on chlorophyll retention under drought stress have been reported in rose by
Al-Yasi et al., (2020); Adamipour et al., (2020); Farahani et al., (2021); Aalam et al., (2024); Shi et al., (2019); Hassan et al., (2017) and
Soundararajan et al., (2017).
Membrane stability index (MSI) declined significantly with increasing drought stress, decreasing from 70.50% under 100% field capacity (FC) to 59.86% at 75% FC and 50.67% at 50% FC (Fig 3A). Foliar application of potassium silicate significantly improved MSI under all irrigation regimes, with 150 mg L
-1 recording the highest values of 72.90% and 62.40% under 75% and 50% FC, respectively. The reduction in MSI under drought stress is associated with oxidative damage and membrane lipid peroxidation, whereas potassium silicate enhanced membrane integrity and reduced oxidative stress, thereby improving drought tolerance. Similar findings have been reported in rose by
Zarif et al., (2025) and
Farahani et al., (2020).
Chlorophyll stability index (CSI) decreased significantly with increasing drought stress, declining from 82.30% under 100% field capacity (FC) to 75.40% under severe drought (50% FC) (Fig 3B). Foliar application of potassium silicate significantly improved CSI under all irrigation levels, with 150 mg L
-1 producing the highest values. Under severe drought, CSI increased from 75.40% in untreated plants to 82.92% following potassium silicate application. The improvement in CSI suggests that potassium silicate enhanced chlorophyll stability by protecting chloroplast membranes and reducing drought-induced oxidative damage
(Liang et al., 2007; Farooq et al., 2009; Zhu and Gong, 2014;
Anjum et al., 2017; Soundararajan et al., 2017; Zarif et al., 2025).
Changes in the drought-responsive traits of Rosa damascena
Epicuticular wax content increased progressively with increasing drought severity and potassium silicate application (Fig 4A). Under well-watered conditions (100% FC), untreated plants recorded 46.27 µg cm
-2 wax content, which increased to 52.34 µg cm
-2 under moderate drought stress (75% FC) and further to 59.60 µg cm
-2 under severe drought stress (50% FC). The increase in epicuticular wax content under moisture stress indicates an adaptive protective response that helps reduce water loss and maintain plant water status under drought conditions. Enhanced wax deposition on the leaf surface may contribute to reducing cuticular water loss and protecting tissues from excessive dehydration
(Wissemann et al., 2007). Drought-induced increases in wax accumulation have been associated with activation of cuticle-related metabolic pathways and enhanced biosynthesis of long-chain hydrocarbons that improve leaf resistance to water loss
(Buschhaus et al., 2007). Foliar application of potassium silicates further enhanced wax accumulation under all irrigation regimes. Under 100% FC, wax content increased from 46.27 µg cm
-2 in untreated plants to 54.80 µg cm
-2 with 200 mg L
-1 potassium silicate. Under moderate drought stress (75% FC), wax content increased from 52.34 µg cm-2 to 60.97 µg cm
-2, while under severe drought stress (50% FC), wax deposition increased from 59.60 µg cm-2 to 68.28 µg cm
-2 following application of 200 mg L
-1 potassium silicate. Among all treatments, the highest epicuticular wax deposition was recorded under severe drought stress combined with 200 mg L
-1 potassium silicate application. Similar increases in epicuticular wax accumulation under water-deficit conditions have been reported in rose and other ornamental crops
(Simoes et al., 2020). These findings suggest that potassium silicate promotes epicuticular wax deposition, which may contribute to drought adaptation.
Total phenol content increased with increasing drought stress, rising from 1225.40 µg GAE g
-1 FW at 100% field capacity (FC) to 1368.20 µg GAE g
-1 FW at 75% FC and 1425.60 µg GAE g
-1 FW at 50% FC (Fig 4B). Foliar application of potassium silicate significantly reduced phenol accumulation under all irrigation regimes, with 150 mg L
-1 recording the lowest values. Under 75% FC, phenol content decreased from 1368.20 to 1186.20 µg GAE g
-1 FW, while under 50% FC it declined from 1425.60 to 1248.30 µg GAE g
-1 FW. However, phenol content increased slightly at 200 mg L-1 compared with 150 mg L
-1. The increased phenol accumulation under drought reflects activation of antioxidant defence against oxidative stress, whereas potassium silicate reduced phenol synthesis by alleviating stress and improving physiological stability
(Hasanuzzaman et al., 2013; Sapre and vakharia, 2016;
Kim et al., 2017). Similar responses have been reported in
Rosa damascena by
Caser et al., (2019) and
Hessini et al., (2022).
Proline content increased significantly with increasing drought stress, rising from 0.86 µmol g
-1 FW at 100% field capacity (FC) to 1.52 µmol g-1 FW at 75% FC and 2.38 µmol g-1 FW at 50% FC (Fig 4C). Foliar application of potassium silicate significantly reduced proline accumulation under all irrigation regimes, with 150 mg L
-1 recording the lowest values. Under 75% FC, proline content decreased from 1.52 to 1.17 µmol g
-1 FW, while under 50% FC it declined from 2.38 to 1.78 µmol g
-1 FW. The increased proline accumulation under drought stress reflects osmotic adjustment and protection against dehydration, whereas potassium silicate alleviated osmotic stress by improving plant water status and membrane integrity
(Farooq et al., 2009; Yokota et al., 2002; Liang et al., 2007). Similar reductions in proline accumulation following silicon application have been reported by
Gunes et al., (2008) and
Kim et al., (2017), indicating improved physiological stability and drought tolerance.
Correlation analysis of physiological and drought-responsive traits of Rosa damascena
Correlation analysis showed significant relationships among the physiological and drought-responsive traits of
Rosa damascena under drought stress and potassium silicate application (Fig 5). Relative water content (RWC) was positively correlated with chlorophyll-a (r = 0.91), chlorophyll-b (r = 0.91), total chlorophyll (r = 0.91), membrane stability index (MSI; r = 0.97) and chlorophyll stability index (CSI; r = 0.89). Chlorophyll pigments were also strongly correlated with each other (r = 1.00) and positively associated with MSI and CSI, indicating improved photosynthetic efficiency and membrane stability
(Farooq et al., 2009; Al-Yasi et al. (2020);
Liang et al., 2007; Soundararajan et al., 2017; Hassan et al., 2017; Tamilselvan et al., 2024). In contrast, proline and total phenol contents were negatively correlated with the physiological traits, while epicuticular wax was positively correlated with proline (r = 0.74). These relationships indicate that potassium silicate maintained physiological performance while reducing drought-induced biochemical stress, thereby improving drought tolerance in
Rosa damascena (Farooq et al., 2009; Hasanuzzaman et al., 2013; Buschhaus et al., 2007; Wissemann et al., 2007).