Plant height
Plant height increased progressively with crop age and nutrient input (Table 2). At 30 DAS, the tallest plants (25.33 cm) were recorded under T12, followed by T11 (24.33 cm) and T10 (23.00 cm), whereas T1 recorded the minimum (9.00 cm). At 60 DAS, T12 again recorded the maximum height (119.67 cm), followed by T11 (115.00 cm) and T10 (110.67 cm). At maturity, T12 reached 172.00 cm compared with 94.00 cm in T1. The progressive enhancement in plant height with combined inorganic-organic inputs is attributed to improved nitrogen and phosphorus availability, better soil moisture retention and stimulation of beneficial soil microflora that promote cell elongation and apical meristem activity (
Mehta and Singh, 2019;
Mondal et al., 2015). Similar responses to nutrient management and sulphur nutrition have been reported in mustard
(Thaneshwar et al., (2017) and
Arya et al., (2007); Chandel et al., 2019; Keerthi et al., 2017; Saral et al., 2025).
Number of leaves and branches per plant
The number of leaves plant
-1 followed a similar treatment response to plant height (Table 2). Maximum leaves at maturity (17.67) were recorded under T12, followed by T10 and T11 (17.33 each), while T1 and T2 recorded the minimum (11.00 each). Number of branches at maturity was highest in T11 (14.33) and T12 (14.00) and lowest in T1 and T2 (5.33 each). The greater branching under integrated nutrient treatments may be associated with improved nutrient availability and greater vegetative growth. Comparable positive responses of growth attributes to integrated or sulphur-based nutrient management have been reported in mustard
(Shorna et al., 2020; Dongrawar et al., 2007; Rundal et al., 2013; Chandel et al., 2019).
Yield attributes and crop yield
The number of siliquae plant
-1 differed significantly among treatments (Table 3). The maximum value was recorded in T11 (337.67), followed by T12 (316.00) and T10 (313.33), while T1 recorded the minimum (109.33). Siliqua length was maximum in T11 and T12 (8.67 cm each) and minimum in T1 (3.67 cm). Seeds siliqua
-1 were highest in T12 (17.00) and were statistically at par with T9, T10 and T11 (16.67 each). Test weight showed a non-significant trend, ranging from 3.48 g in T1 and T2 to 3.99 g in T11. The improvement in yield attributes under integrated nutrient supply is consistent with earlier reports for mustard
(Kasved et al., (2010); Manna and Siddique, 2025).
Grain yield increased significantly with increasing intensity of integrated nutrient inputs. T12 recorded the highest grain yield (22.33 q ha
-1), followed by T11 (22.00 q ha
-1) and T10 (21.00 q ha
-1), which were statistically at par, whereas T1 recorded the minimum (10.67 q ha
-1). Thus, T12 produced 109% higher grain yield than the control. The higher yield under T12 may be attributed to the combined supply of nutrients from NPK, sulphur, vermicompost and FYM, which supported vegetative growth and reproductive development (
Aulakh, 2010;
Basu and Patel, 2022). The role of sulphur in mustard productivity is well established and recent work has demonstrated positive responses of
Brassica crops to sulphur-based nutrient management
(Chandel et al., 2019; Saral et al., 2025; Manna and Siddique, 2025). Stover yield was highest in T11 and T12 (42.67 q ha
-1 each) and lowest in T1 (19.67 q ha
-1). Harvest index ranged from 31.36% in T6 to 36.46% in
(Maheshbabu et al., 2008).
Insect pest population
Insect population increased with increasing intensity of organic amendment across the observed growth stages (Table 3). At 30 DAS, T12 recorded the highest observed population (12.83 insects plant
-1), whereas T1 recorded 4.17 insects plant
-1. At 60 DAS, T12 recorded 15.88 insects plant
-1 compared with 10.12 insects plant
-1 in T1. At maturity, T12 (14.25), T11 (14.08) and T10 (13.45) had the highest observed populations. Five pest species were observed:
Lipaphis erysimi,
Athalia lugens proxima,
Bagrada hilaris,
Pieris rapae and Plutella xylostella. The higher pest counts in treatments supporting greater crop growth may be associated with differences in canopy development and plant nutritional status; however, these mechanisms were not directly measured in the present experiment and should therefore be interpreted as plausible explanations rather than demonstrated causal effects. The pest observations reinforce the need to combine nutrient management with regular monitoring and need-based integrated pest management, consistent with the broader emphasis on integrated pest protection in oilseed crops
(Obermeier et al., 2022; Golizadeh et al., 2025).
Correlation
Pearson correlation analysis showed strong positive treatment-level associations between crop performance and insect population (Table 4). Grain yield was positively correlated with insect population at 30 DAS (r = 0.979), 60 DAS (r = 0.857) and maturity (r = 0.971), while plant height at maturity was correlated with insect population at 30 DAS (r = 0.870), 60 DAS (r = 0.942) and maturity (r = 0.886). Grain yield and stover yield were also strongly correlated (r = 0.972). With 12 treatment means, all reported correlation coefficients were significant at P<0.001. These associations indicate that treatments producing greater crop growth and yield also tended to have greater insect populations; they do not, by themselves, establish that higher nutrient availability caused insect multiplication. Therefore, integrated nutrient management should be accompanied by regular pest surveillance and need-based integrated pest management.