Research Article
Assessment of Key Brinjal (Solanum melongena L.) Cultivars Against Sucking Insect Pests and Economic Analysis Under Field Conditions in Peshawar, Pakistan
Mehran Ullah1* and Muhammad Anwar Khan1
1Department of Plant Protection, Faculty of Crop Protection sciences, The University of Agriculture, Peshawar, Pakistan.
Abstract | An experiment was conducted to study the population dynamics of sucking insect pests along with economic parameters on key brinjal cultivars at Newly Developmental Farms (NDF), The University of Agriculture Peshawar. Six different treatments, i.e., Nirala (T1), Shamli hybrid (T2), Cluster king (T3), Purple long (T4), Dilnasheen (T5) and Bemisaal (T6) were cultivated in randomized complete block design (RCBD) with three replications. Data were collected on the population dynamics of aphids (Aphis gossypii), jassids (Amrasca biguttula), whiteflies (Bemicia tabaci), host plant susceptibility index (HPSI), yield (ton ha-1) and cost-benefit analysis, respectively. Results regarding the time interval data indicated that the highest insect populations were recorded in May. While screening results showed that Nirala and Shamli hybrid cultivars were found resistant against sucking insect pests of brinjal crops, it resulted in the lowest host plant susceptibility indices (HPSIs), higher yields, and the maximum cost-benefit ratio among the six tested cultivars. Thus, it can be hypothesized that Nirala and Shamli hybrid brinjal cultivars are highly resistant against sucking insect pest of brinjal crop and can be recommended for inclusion in integrated pest management (IPM) and sustainable development programs to minimize pest damage and improve brinjal production.
Received | Jun 14, 2025; Accepted | Sep 4, 2025; Published | December 08, 2025
*Correspondence | Mehran Ullah, Department of Plant Protection, Faculty of Crop Protection sciences, The University of Agriculture, Peshawar, Pakistan; Email: [email protected]
Citation | Ullah, M. and M.A. Khan. 2025. Assessment of key brinjal (Solanum melongena L.) cultivars against sucking insect pests and economic analysis under field conditions in Peshawar, Pakistan. Sarhad Journal of Agriculture, 41(5): 01-13.
DOI | https://dx.doi.org/10.17582/journal.sja/2025/41.5.01.13
Keywords | Brinjal, Climatic conditions, Relative humidity, Sucking insect Pest, Temperature.
Copyright: 2025 by the authors. Licensee ResearchersLinks Ltd, England, UK.
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Introduction
Brinjal, Solanum melongena Linnaeus is commonly grown vegetable of Solanaceae family also known as Aubergine (Kantharajha and Golegaonkar, 2004) cultivated in tropical and subtropical climatic zones (Kaushik et al. 2016). The Solanaceae family comprises approximately 2,450 species distributed across 95 genera, cultivated globally (Mabberley, 2008). Eggplant is rich in essential nutrients, including iron, calcium, phosphorus, potassium, vitamin B, water, protein, fiber, fat, minerals, carbohydrates, folic acid, ascorbic acid, and riboflavin (Bhatti et al. 2013). Extracts from brinjal are employed in traditional medicine for conditions such as diabetes, gonorrhea, cholera, bronchitis, diarrhea, and hemorrhoids. Chlorogenic acid, a bioactive compound in eggplant, exhibits anticancer, cardioprotective, anti-obesity, analgesic, cholesterol-lowering, and antioxidant properties (Bello et al., 2005; Suroowan et al., 2019).
Globally, approximately 1.57 billion hectares of land are dedicated to crop cultivation, whereas in Pakistan, 30.94 million hectares are allocated for this purpose, Similarly, the global per capita cropland average is 0.20 hectares, while Pakistan falls below this average at 0.13 hectares per capita (FAO, 2024). The data indicate a progressive increase in the total cultivated area and production of vegetables in Pakistan over time. Between 2000-01 and 2017-18, the vegetable cultivation area expanded by 24%, while production exhibited a more substantial rise of 66% during the same period (GoP, 2018). In 2022, Pakistan’s food exports amounted to 5,103 million USD, while food imports reached 9,070 million USD, resulting in a net trade deficit of 3,968 million USD (FAO, 2024). China, India, Egypt, Turkey, and Iran are the leading producers of eggplant globally, with China contributing 58% of the total production, followed by India at 25%, and significant outputs from Egypt, Turkey, and Iran (Younas et al., 2022). In Pakistan, Brinjal is cultivated over an area of 6,667 hectares, yielding an annual production of 95,001 tons (MNFSR, 2022-23), While in Khyber Pakhtunkhwa province, brinjal cultivation spans 1,045 hectares, producing 7,759 tons annually with average yield of 10.50-ton ha-1 (MNFSR, 2022-23). In Khyber Pakhtunkhwa, brinjal cultivation has shown minimal expansion over the five-year period from 2018-19 to 2022-23, with the cultivated area increasing marginally from 1,039 to 1,045 hectares (MNFSR, 2022-23). Conversely, brinjal production declined from 9,206 tonnes in 2018-19 to 7,759 tonnes in 2022-23. Despite this reduction in production, the average monthly wholesale price of brinjal in the major markets of Peshawar surged from 1,100 to 3,067 Rupees per 40 kg over the same period (MNFSR, 2022-23). Khyber Pakhtunkhwa’s diverse climate, with temperatures ranging from below 0°C in the north to over 45°C in the south, supports a wide variety of crops, fruits, and vegetables, offering significant potential for the vegetable sector if proper attention is given and quality factors are addressed (Jalal-ud-Din, 2011).
The fructification cycle of eggplant is completed within three months. As a warm-season crop, eggplant thrives under a photoperiod of 10–12 hours and an optimal temperature range of 23°C-26°C however low temperatures of 10°C–12°C negatively influenced the growth of flowering and fruit sets (Sekara et al., 2007; Singh, 2018), these temperature ranges showed that brinjal cultivation is perfectly suitable for the climatic conditions Khyber Pakhtunkhwa, Pakistan. Eggplant height ranges from 0.4 to 1.5 meters, characterized by branching stems and broad leaves. Similarly, flowers of eggplant are hermaphroditic or male, complete, actinomorphic, star-shaped, and can be either hypogynous or epigenous. They may appear as solitary blooms or in clusters of 3 to 5 flowers. Flower diameter ranges from 3 cm to 5 cm (Daunay et al., 2001; Hassan et al., 2015).
In Pakistan, from cultivation till harvest, brinjal crops are severely damaged by various insect pests (Rai et al., 2014), among which, aphids (Aphis gossypii), jassids (Amrasca biguttula), thrips (Thrips palmi Karny), brinjal stem borer (Euzophera perticella Ragonot), fruit and shoot borer (Leucinodes orbonalis Guenee), leaf roller (Eublemma olivacea Walker) and whitefly (Bemicia tabaci Genn.) are the most important (Mehmood et al., 2002; FAOSTAT, 2010; Prasad et al., 2017; Yousafi et al., 2020; Ullah et al., 2022). Under the climatic conditions of Peshawar, B. tabaci, A. biguttula biguttula, A. gossypii, and L. orbonalis are the primary insect pests causing substantial damage to various brinjal (Solanum melongena L.) cultivars, including Shamli, Pearl Long, Local long, Black Neelam, Purple long and Black Beauty (Habib et al., 2015; Ayub et al., 2020 and Ullah et al., 2022).
A. gossypii both nymph and adult present on the lower side of leaf damaging young shoots and leaf surfaces by sucking cell sap. Light infestation results in yellowing of leaves while severe infestation causes leaf curling and deformation; also produces honeydew which leads to the development of soot mold fungi and disturbs the process of photosynthesis (Srinivasan, 2009). Aphids attack the crop at 35-40 days after transplanting (Choudhury et al., 2015). At the seedling stages of the crop, larvae attack foliar, while in later stages, flower buds and fruits are also attacked due to which the production is severely affected (Yousafi et al., 2020). In the months of July-October, 60% damages are caused by this pest to brinjal crop (Dhandapani et al., 2003). A. biguttula biguttula adult feed on the lower side of the leaves by sucking the sap from the plant, results in curling and yellowing of leaf by injecting the toxic material which lead to necrosis and ultimately causes almost 54% damage to brinjal crop (Khan et al., 2015 and Chand et al., 2024). Jassid infestation stunts plant growth, reduces bud and flower production, lowers yield, and transmits the mycoplasmal disease ‘little leaf’ resulting in significant economic losses (Thakar et al., 2024). B. tabaci is highly polyphagous as both nymphs and adults feed on plant sap, leading to reduced plant vigor. Severe infestations cause leaf yellowing and abscission. This diurnal insect typically rests on the underside of leaves during nighttime. (Srinivasan, 2009).
Molecular, morphological and biochemical markers are used to evaluate the diversity and economic parameters in different cultivars of brinjal crops. Morphological markers are defined as observable physical traits, that are used to assess interspecific and intraspecific diversity (Prohens et al., 2005; Ullah et al., 2014). Data regarding the population dynamics of insect pest should be collected from randomly selected plants within each plot arranged in a randomized complete block design (Yousafi et al., 2020). Weekly data collection on the population dynamics of sucking insect pests facilitates the identification of resistant brinjal (Solanum melongena L.) cultivars (Yousafi et al., 2013). Furthermore, data should be conducted during early morning hours when the activity levels of the pests are minimal (Ashraf et al., 2017). The host plant susceptibility indices (HPSIs) are a critical metric for identifying susceptible cultivars among the tested brinjal varieties (Ali et al., 2014). The population dynamics of sucking insect pests exhibits temporal variation across different brinjal cultivars (Yousafi et al., 2013). Similarly, data regarding yield also exhibits significant variation on different cultivars of brinjal crop (Ali et al., 2014).
Synthetic chemicals such as organophosphates, pyrethroids, neonicotinoids and insect growth regulators are commonly used to control pests like aphids, whiteflies, borers and mites (Dwarka et al., 2024). The application of Bacillus thuringiensis (Bt), Methoxyfenozide, and Emamectin Benzoate effectively reduces general pest damage, leading to increased brinjal yield (Sahu et al., 2023). Chemical Insecticides are commonly used against aphids, jassids and whiteflies, but they are costly, environmentally harmful, contribute to resistance, and have adverse effects on beneficial insects (Hrynko et al., 2021 and Ullah et al., 2022).
Biological control utilizes natural enemies of insect pest, including predators, parasitoids and entomopathogens, for sustainable pest management (Dwarka et al., 2024). Predators like coccinellids and lacewings regulate aphid and whitefly populations, while endo-parasites such as Arescon enocki and Chrysoperla spp. effectively control jassids (Sahito et al., 2018). Orius insidiosus suppresses thrips, and parasitoids like Encarsia formosa, Eretmocerus spp., and Chrysocharis pentheus aid in managing B. tabaci population (Raina and Yadav, 2018). Extracts of A. indica, E. globulus, and M. pulegium have demonstrated significant efficacy, reducing aphid, jassid, and leaf hopper populations by 93–97%, 87–92%, and 25–73%, respectively (Maqsood et al., 2023). Plant-based products, both crude and purified, have proven effective as herbicides, fungicides and bactericides (Jabeen et al., 2021; Javaid et al., 2022 and Saeed et al., 2023), with recent studies highlight their effectiveness against insect pests, leading to higher production and improved cost-benefit analysis in brinjal cultivation (Maqsood et al., 2023).
One of the most important factors in integrated pest management (IPM) strategies is host plant resistance which is environmentally friendly and can be used alone or in combination (Barzman et al., 2015). Host Plant Resistance enhances integrated pest management (IPM) by reducing insecticide use and promoting natural enemy efficacy, where even low plant tolerance significantly decreases the need for chemical control (Deguine et al., 2021). Host plant resistance can render crops unsuitable for insect pests without inducing inheritable resistance within the pest population (Mani et al., 2022). Morphological and biochemical characteristics of plants significantly contribute to resistance; for instance, leaf trichome length on midrib, thickness of leaf lamina, nitrogen and manganese percentage exhibits a negative correlation with insect pest populations (Mani et al., 2022 and Shah et al., 2023). The selection of resistance cultivars is one of the most important methods of integrated pest management (Maqsood et al., 2023). Screening of several cultivars has been carried out by researchers and growing resistance cultivars has been recommended by these experts (Shaukaet et al., 2018 and Younas et al., 2022). Brinjal is favored by breeders for its resilience, hardy nature, large flowers, and high seed yield from a single pollination event (Farooq and Delvadiya, 2023). The economic viability of brinjal cultivation has been enhanced by the cost-effective production of F1 seeds and the low seed requirement per unit area (Mishra et al., 2023). Enhancing pest resistance in plants is vital for sustainable agriculture, reducing pesticide use, improving crop yields, and promoting environmental and food security (Kumari et al., 2022). Keeping in view the importance of resistance cultivars, an experiment was conducted to record the economic parameters and population dynamics of A. gossypii, A. biguttula biguttula and B. tabaci on six important cultivars of brinjal crops.
Materials and Methods
An experiment was conducted to study the population dynamics of aphids (Aphis gossypii), whitefly (Bemicia tabaci) and jassids (Amrasca biguttula) along with economic parameters on six different brinjal cultivars at Newly Developmental Farms (NDF), The University of Agriculture Peshawar. Six different treatments, i.e., Nirala (T1), Shamli hybrid (T2), Cluster king (T3), Purple long (T4), Dilnasheen (T5) and Bemisaal (T6) were used in this experiment to find the resistant cultivar against sucking insect pests. The experiment was conducted in Randomized Complete Block design (RCBD) with three replications. Distance between row to row and plant to plant was kept 60 cm and 50 cm, respectively. A buffer zone of 2ft was kept isolating treatments and replications. During the cropping season, agronomic practices were carried out in each treatment.
Population dynamics of aphids, jassids and whiteflies
Five plants from each replication were selected and tagged for recording data on aphids (nymph + adult), jassids (nymph + adult), and whiteflies (nymph + adult). Data collection did not include the nursery period. Observations were made biweekly over a four-month period, starting from the commencement of the experiment. Three leaves (one each from the top, middle, and bottom) were randomly selected per plant, and the number of sucking insect pests were recorded visually in the early morning when insect activity was minimal. The mean population density of sucking insect pest was calculated for each block. (Ashraf et al., 2017; Yousafi et al., 2020).
Host plant susceptibility indices (HPSIs)
The host plant susceptibility index (HPSI) was calculated to assess the per-leaf vulnerability of selected brinjal cultivars to sucking insect pests. Individual and cumulative indices were determined using Microsoft Excel on an IBM-compatible system. The HPSI (%) was derived using the formula (Ali et al., 2014):

Where:
Fruits were harvested at 1–2 cm width and 5–10 cm length, while overripe fruits, identified by a brown hue, spongy texture, and crinkled skin, were excluded. In three replicates, mature, healthy fruits were collected weekly. Fruits from each treatment were weighed using an electronic balance, and the average yield was calculated in ton ha-1 (Ullah et al., 2022).
Cost-benefit analysis
For the calculation of cost benefit ratio, input expenses for land preparation, seeds, and labor required from cultivation to harvest were recorded as unit costs per hectare. The market value of brinjal was calculated based on wholesale prices in Peshawar. The Cost-Benefit Ratio (CBR) was computed using standard methodology.
|
Treatments |
Marketable Yield (kg ha-1) |
Gross revenue in rs. per ha=marketable yield x price kg-1) |
Total cultivation cost |
CBR=Gross revenue/cultivation cost |
Statistical analysis
All the recorded data were analyzed statistically by using two factorial Randomized Complete Block Design (RCBD) in STATISTIX (8.1) software. Means were separated by using Least Significance Difference Test at 5% level of significance (Steel and Torrie, 1980).
Results and Discussion
Population trend of aphids (A. gossypii) leaf-1 on six different brinjal cultivars under field conditions at Newly Developed Malakandair Farms, Peshawar.
Table 1: Aphid (Aphis gossypii) population trends leaf-1 on six brinjal cultivars under field conditions at newly developed malakandair farms, Peshawar.
|
Cultivar |
Time interval |
Mean |
|||||||
|
15th Mar |
1st Apr |
15th Apr |
1st May |
15th May |
1st June |
15th June |
1st July |
||
|
Nirala (T1) |
6.99q |
13.33l |
16.62ij |
17.04i |
13.16l |
8.80p |
5.81r |
3.23s |
10.62e |
|
Shamli hybrid (T2) |
5.79r |
12.28mn |
15.78k |
16.71ij |
12.27o |
7.65q |
5.91r |
2.97s |
9.85 e |
|
Cluster king (T3) |
12.27mn |
19.19g |
26.09c |
26.35c |
15.98jk |
13.03lm |
8.74p |
3.56s |
15.65c |
|
Purple long (T4) |
8.79p |
16.71ij |
23.31ef |
23.55e |
15.70k |
11.05o |
7.16q |
3.10s |
13.67d |
|
Dilnasheen (T5) |
16.02jk |
23.90 |
29.86b |
29.52b |
22.74f |
17.11i |
11.64no |
6.96q |
19.72b |
|
Bemisaal (T6) |
19.38g |
24.83d |
34.65a |
34.54a |
26.17c |
18.24h |
11.12o |
7.34q |
22.03a |
|
Mean |
11.53c |
18.37b |
24.38a |
24.69a |
17.50b |
12.64c |
8.40d |
4.52e |
|
Those means which have the same alphabet are not statistically different from one another at 5% level of significance using LSD test (P < 0.05)
LSD for cultivars= 1.2742
LSD for time interval= 1.3166
LSD for cultivars*time interval= 0.7756
Table 2: Jassids (Amrasca biguttula biguttula) population trends leaf-1 on six brinjal cultivars under field conditions at newly developed malakandair farms, Peshawar.
|
Cultivar |
Time interval |
Mean |
|||||||
|
15th Mar |
1st Apr |
15th Apr |
1st May |
15th May |
1st June |
15th June |
1st July |
||
|
Nirala (T1) |
1.44stu |
2.65no |
3.75j |
3.83ij |
2.22pq |
2.49o |
1.17wx |
0.33y |
2.23e |
|
Shamli hybrid (T2) |
1.55rst |
2.78mn |
3.93hi |
3.99hi |
231p |
2.51o |
1.24vwx |
0.36y |
2.33d |
|
Cluster king (T3) |
2.19pq |
3.21kl |
4.77ef |
4.69efg |
3.09l |
3.31k |
1.61r |
1.20wx |
3.01c |
|
Purple long (T4) |
2.18pq |
3.23kl |
4.77ef |
4.84e |
3.13l |
3.33k |
1.60rs |
1.13x |
3.03c |
|
Dilnasheen (T5) |
3.17kl |
5.10d |
7.15b |
7.36a |
4.62fg |
4.77ef |
2.15pq |
1.39tuv |
4.46a |
|
Bemisaal (T6) |
2.83m |
4.59g |
6.59c |
7.13b |
4.02h |
4.01h |
2.08q |
1.31uvw |
4.07b |
|
Mean |
2.23e |
3.59c |
5.16a |
5.31a |
3.23e |
3.41d |
1.64e |
0.95ef |
|
Those means which have the same alphabet are not statistically different from one another at 5% level of significance using LSD test (P < 0.05)
LSD for cultivars= 0.1953
LSD for time interval= 0.3592
LSD for cultivars*time interval= 0.1676
The results indicate that the population of A. gossypii leaf-1 varied significantly among six brinjal cultivars (Table 1). The highest mean population of A. gossypii leaf-1 was observed on the Bemisaal cultivar followed by Dilnasheen and Cluster king cultivars, respectively. In contrast, the lowest mean population of A. gossypii leaf-1 was recorded on the Shamli hybrid, followed by the Nirala cultivar, with no significant difference between these two cultivars. The perusal of data regarding time interval demonstrated that A. gosyypii peaked at the end of April and during the first half of May and diminished during the month of July. Additionally, it was revealed that A. gossypii exhibited significantly higher population on the Bemisaal cultivar throughout the experiment, whereas the lowest densities were observed on the Shamli hybrid cultivar. Our results are in conformity with Habib et al. (2015) who observed the infestation of A. gossypii three weeks after transplanting, with the maximum infestation recorded in mid-May on different brinjal cultivars. Similarly, Patel et al. (2015) reported aphid infestation from the beginning to the termination of the crop cycle, recording the highest population density in May. The findings of this study on the susceptibility and resistance of brinjal cultivars align with those of Yousafi et al. (2020), who reported that the Nirala cultivar exhibited significant resistance to A. gossypii compared to the Bemisaal and Dilnasheen cultivars. Similarly, Ayub et al. (2020) found the Shamli hybrid cultivar resistant, aligning with our findings, but reported the Purple Long cultivar as highly susceptible, whereas our study classified it as moderately resistant among six tested cultivars. They also observed that the A. gossypii population peaked during the second week of May and declined by the end of June. Beyond chemical control, botanicals like A. indica have been extensively studied, with azadirachtin identified as a key insecticidal compound. It acts as a repellent, antifeedant, and sterilizing agent (Chaudhary et al., 2017) as well as various bioactive compounds from A. indica leaves contribute to its insecticidal properties (Ahmad et al., 2019 and Khan and Javaid, 2021).
Population trend of jassids (amrasca biguttula) leaf-1 on six different brinjal cultivars under field conditions at newly developed malakandair farms, Peshawar
The results indicate significant variation in the population of A. biguttula biguttula leaf-1 among the tested brinjal cultivars (Table 2). The highest mean population of A. biguttula biguttula leaf-1 was observed on the Dilnasheen brinjal cultivar, followed by Bemisaal, Purple Long, and Cluster King brinjal cultivars, respectively. However, significantly lowest mean population density was recorded on the Nirala cultivar, followed by the Shamli hybrid brinjal cultivar. The analysis of the time interval data revealed that the population of A. biguttula biguttula reached its peak at the end of April and during the first half of May, subsequently declining in July. Furthermore, it was revealed that A. biguttula biguttula consistently exhibited higher populations on the Dilnasheen cultivar throughout the experiment, whereas the lowest densities were observed on the Nirala brinjal cultivar. The findings of this study on the susceptibility and resistance of brinjal cultivars align with those of Yousafi et al. (2013), who reported that the Nirala cultivar exhibited significant resistance to A. biguttula biguttula compared to the Bemisaal and Dilnasheen cultivars. Similarly, Ashraf et al. (2017) reported that Shamli hybrid brinjal cultivar showed resistance to A. biguttula biguttula as compared to tested cultivars. Our results regarding A. biguttula biguttula population ranging from 2.23 to 4.46 leaf-1, differ from Elanchezhyan et al. (2008), who reported a range of 0.00 to 6.80 per leaf across 25 brinjal varieties, likely due to differences in varieties and experimental locations. Our findings regarding the time interval align with Ali et al. (2016), who reported that A. biguttula biguttula infestation began in April, peaked in May, and declined by late June. Similarly, Mahmood et al. (2002) observed that A. biguttula biguttula populations were positively correlated with high temperatures and negatively correlated with rainfall. Halder et al. (2023) investigated the effects of entomopathogenic fungi, botanicals, and chemicals, reporting the lowest jassid (1.77, 2.33/leaf) and whitefly (1.41, 1.63/leaf) populations in plots treated with entomopathogenic fungi, comparable to (Chemical) Imidacloprid.
Population trend of whiteflies (bemicia tabaci) leaf-1 on six different brinjal cultivars under field conditions at newly developed malakandair farms, Peshawar.
The results indicate that the population density of B. tabaci leaf-1 varied significantly across six brinjal cultivars (Table 3). The maximum mean population density was recorded on the Bemisaal cultivar, followed by Dilnasheen, Cluster King, and Purple Long brinjal cultivars. In contrast, the minimum mean population density was observed on the Nirala, followed by the Shamli hybrid cultivar. The data regarding time interval indicated that the population of Aphis gossypii remains significantly higher during
Table 3: Whitefly (Bemicia tabaci) population trends leaf-1 on six brinjal cultivars under field conditions at newly developed malakandair farms, Peshawar.
|
Cultivar |
Time interval |
Mean |
|||||||
|
15th Mar |
1st Apr |
15th Apr |
1st May |
15th May |
1st June |
15th June |
1st July |
||
|
Nirala (T1) |
7.48t |
8.66rs |
11.54n |
14.72gh |
13.87ij |
9.32pqr |
4.49vw |
3.90w |
8.25e |
|
Shamli hybrid (T2) |
7.50t |
8.74rs |
12.08mn |
14.93g |
14.08hi |
9.86p |
5.04v |
3.90w |
9.51d |
|
Cluster king (T3) |
8.29s |
9.86p |
13.13kl |
17.92d |
17.21e |
13.64ijk |
9.07qr |
6.11u |
11.90c |
|
Purple long (T4) |
8.36s |
9.63pq |
12.52lm |
18.27cd |
16.51ef |
13.27jk |
8.91rs |
5.97u |
11.68c |
|
Dilnasheen (T5) |
10.65o |
14.85g |
18.85c |
26.93a |
26.44a |
18.41cd |
12.15mn |
6.62u |
16.86b |
|
Bemisaal (T6) |
14.02hi |
15.12f |
20.84b |
26.71a |
27.01a |
18.80c |
13.89ij |
6.66u |
18.01a |
|
Mean |
9.38f |
11.31e |
14.83c |
19.91a |
19.19b |
13.88d |
8.92g |
5.53h |
|
Those means which have the same alphabet are not statistically different from one another at 5% level of significance using LSD test (P < 0.05)
LSD for cultivars= 0.2503
LSD for time interval= 0. 2890
LSD for cultivars* time interval = 0.7079
the month of May and gradually declined by July. Additionally, it was revealed that B. tabaci consistently exhibited higher populations on the Bemisaal cultivar throughout the experiment, while the lowest densities were recorded on the Nirala cultivar. Muthukumar and Kalyanasundaram, (2003) stated that B. tabaci appeared initially after the first week of transplanting and remained active throughout the cropping season. Our findings align with Ayub et al. (2020), who reported the Shamli hybrid as resistant to B. tabaci. However, they classified the Purple Long as resistant cultivar against B. tabaci, whereas our study categorized it as moderately susceptible among the six tested cultivars. Both studies observed similar trends regarding the peak population of B. tabaci. Furthermore, Patel et al. (2015) have demonstrated a positive correlation between B. tabaci populations and maximum and minimum temperatures, and a negative correlation with rainfall and relative humidity. Abubakar et al. (2023) studied the eco-friendly management of B. tabaci and revealed that neem leaf extract (60ml/L) was found highly effective against whiteflies (1.2-1.3 adults leaf-1) resulting in better production.
Host plant susceptibility indices (HPSIs) of six different brinjal cultivars against sucking insect pest under field conditions.
The host plant susceptibility indices (HPSI) based on the population densities of A. gossypii, A. biguttula biguttula, and B. tabaci across six brinjal cultivars are presented in Figure 1. The results indicate that the Bemisaal genotype exhibited the highest HPSI values, at 23.20% for B. tabaci, 23.51% for A. biguttula biguttula, and 24.06% for A. gossypii, identifying it as the most susceptible cultivar, followed by Dilnasheen. In contrast, the lowest HPSI values were recorded for Nirala, with 11.97% for B. tabaci and 11.77% for A. biguttula biguttula, and for Shamli hybrid, with 10.75% for A. gossypii, followed by Purple Long and Cluster King cultivars. These findings are consistent with the results of Ali et al. (2014), who categorized various brinjal cultivars into resistant and susceptible groups based on host plant susceptibility indices (HPSIs). Based on the HPSI results, two cultivars, Nirala and Shamli Hybrid, were identified as resistant, while Cluster King and Purple Long exhibited intermediate resistance. While, the remaining cultivars, Bemisaal and Dilnasheen, were classified as susceptible to sucking insect pests of brinjal crops. Furthermore, through host plant resistance, insect damage has been minimized (Mouden et al., 2017). Resistant eggplant varieties possess thick, elongated clasping calyxes that hinder larval penetration (Dar et al., 2017). Narrow, elongated, and hairy fruits exhibit lower infestation rates due to reduced pest preference for oviposition (Gautam et al., 2019). Additionally, pericarp thickness shows a positive correlation with infestation, whereas trichome density is negatively correlated (Challa et al., 2021).
Table 4: Impact of six different brinjal cultivars on fruit Yield (ton ha-1) under field condition at newly developed malakandair farms, Peshawar.
|
Treatments |
Yield plant-1 |
Yield (Ton ha1) |
|
Nirala (T1) |
1.079 a |
14.953 a |
|
Shamli hybrid (T2) |
0.933 b |
13.477 b |
|
Cluster king (T3) |
0.768 c |
10.407 c |
|
Purple long (T4) |
0.817c |
10.627 c |
|
Dilnasheen (T5) |
0.501 d |
7.653 e |
|
Bemisaal (T6) |
0.447 d |
8.263 d |
|
LSD |
0.1031 |
0.4511 |
|
F |
56.16 |
398.98 |
|
P-Value |
0.0000 |
0.0000 |
Impact of six different brinjal cultivars on fruit Yield (ton ha-1)
Fruit yield is a critical parameter from the perspective of farmers’ economics. A significant variation in yield (ton ha-¹) was observed among the six brinjal cultivars (Table 4). The Nirala cultivar recorded the highest yield (14.95-ton ha-¹), followed by the Shamli hybrid (13.47-ton ha-¹). However, the Dilnasheen cultivar exhibited the lowest yield (7.65-ton ha-¹), followed by the Bemisaal and Cluster King cultivars, with yields of
Table 5: The Cost-benefit ratio of six various brinjal cultivars under field conditions at at newly developed malakandair farms, Peshawar.
|
Treatments |
Marketable yield (kg ha-1) |
Gross revenue in rs. ha-1 = marketable yield x price kg-1 |
Total cultivation cost |
CBR=Gross revenue/cultivation cost |
|
Nirala (T1) |
14953 |
448590 |
76514 |
1:5.86 |
|
Shamli hybrid (T2) |
13477 |
404310 |
79864 |
1:5.06 |
|
Cluster king (T3) |
10407 |
312210 |
75284 |
1:4.14 |
|
Purple Long (T4) |
10627 |
318810 |
76145 |
1:4.18 |
|
Dilnasheen (T5) |
7653 |
229590 |
77689 |
1:2.95 |
|
Bemisaal (T6) |
8263 |
247890 |
77468 |
1:3.19 |
Average wholesale market brinjal price kg-1 in Peshawar= Rs. 30/-
8.26 and 10.40-ton ha-¹, respectively. These findings are consistent with those of Rehman et al. (2019), who reported the highest fruit yield plant-1 for the Nirala cultivar as compared to other tested cultivars. Similar results were also documented by Javed et al. (2017). However, the observed fruit yield per plant differs from the findings of Kundu et al. (2023), who reported yields ranging between 1.08 and 7.65 kg plant-1. This variation may be due to differences in the tested brinjal cultivars and the environmental conditions at the experimental sites.
Effect of six different brinjal cultivars on Cost-benefit ratio
Table 5 summarizes the cost-benefit ratio analysis for the six tested brinjal cultivars. The data reveal that the Nirala cultivar achieved the highest cost-benefit ratio (1:5.86), followed by the Shamli hybrid (1:5.06). In contrast, the Dilnasheen cultivar exhibited the lowest cost-benefit ratio (1:2.95), followed by Bemisaal (1:3.19), Cluster King (1:4.14), and Purple Long (1:4.18), respectively. These results are in agreement with the findings of Gogoi et al. (2018), who reported significant variation in the cost-benefit ratio among different brinjal cultivars, with values ranging from a maximum of 5.35 to a minimum of 0.92, respectively. Similar findings were reported by Sahu et al. (2022), who conducted an evaluation of different brinjal cultivars and reported significant variability in the economic performance of the tested cultivars as highest cost-benefit ratio recorded was 3.87, while the lowest cost-benefit ratio observed was 1.06, respectively. Athawale et al. (2023) reported the highest cost-benefit ratio of 2.64 in small-scale farms, followed by 2.52 in medium-scale and 2.47 in large-scale farms. Yousafi et al. (2016) reported the highest cost-benefit ratio of 1:5.40 in plots treated with Emamectin Benzoate applied four times, followed by Spinosad with a ratio of 1:3.72. Cultural practices significantly influence the cost-benefit analysis of brinjal, with the highest benefit ratio (1:6.3) observed in plots implementing mulching and clipping, compared to the control (1:1.8) (Muhammad et al., 2021).
These results align with the current study, further emphasizing the influence of cultivar selection on economic outcomes in brinjal production.
Conclusions and Recommendations
Nirala and Shamli hybrid demonstrated resistance to sucking insect pests of brinjal crops, exhibiting the lowest host plant susceptibility indices, higher yields, and the maximum cost-benefit ratio among the six tested cultivars. Thus, it can be hypothesized that Nirala and Shamli hybrid brinjal cultivars are highly resistant against A. gossypii, A. biguttula and B. tabaci and can be recommended to farmers for the commercial production and inclusion in integrated pest management (IPM) programs under the climatic conditions of Peshawar. Furthermore, Climate change is anticipated to influence pest distribution and severity, necessitating the development of pest forecasting models and climate-resilient brinjal varieties for effective pest management.
Acknowledgments
The authors express their gratitude to Prof. Dr. Inam Ullah, Department of Agronomy, Farm Manager at the Newly Developmental Farms (NDF), The University of Agriculture Peshawar, for his valuable support and technical guidance throughout the research.
Novelty Statement
This study aims to identify the most resistant brinjal cultivar against sucking insect pests with superior economic parameters and to recommend that cultivar to farmers for commercial production under the climatic condition of Peshawar.
Author’s contribution
Muhammad Anwar Khan: Designed and supervised the experiment.
Mehran Ullah: Conducted the experiment, analyzed data, and wrote the manuscript. All authors read and approved of the final manuscript.
Generative AI or AI assisted technology statement
No AI technology has been used in this whole experimental research trial.
Conflict of Interest
The authors declares that there is no conflict of interest regarding the publication of this article
References
Abubakar, M., D. Yadav, B. Koul and M. Song. 2023. Efficacy of eco-friendly bio-pesticides against the whitefly Bemisia tabaci (Gennadius) for sustainable eggplant cultivation in Kebbi State, Nigeria. Agron., 13(12): 3083. https://doi.org/10.3390/agronomy13123083
Ahmad, S., A. Maqbool, A. Srivastava and S. Gogoi. 2019. Biological detail and therapeutic effect of Azadirachta indica (neem tree) products-a review. J. Evidence-Based Med. Healthcare., 6: 1607-1612 https://doi.org/10.18410/jebmh/2019/324
Alam, S.N., M.A. Rashid, F.M.A. Rouf, R.C. Jhala, J.R. Patel, S. Satpathy, T.M. Shivalingaswamy, S. Rai, I. Wahundeniya, A. Cork, C. Ammaranan and N.S. Talekar. 2003. Development of an integrated pest management strategy for eggplant fruit and shoot borer in South Asia. Shanhua, Taiwan: AVRDC the World Vegetable Center. Techn. Bullet., 28(03): 1-56.
Ali, M., M. Ashfaq, N. Rana, M.S. Haider and M. Amjad. 2014. The susceptibility study of some aubergine (Solanum melongena l.) cultivars against jassid (Amrasca biguttula biguttula (ISHIDA). Pak. J. Agric. Sci., 51(3): 679-683.
Ali, M., M. Ashfaq, M.H. Ranjha, A. Gulzar, S. Ahmad and A. Ali. 2016. The host plant susceptibility indices and varietal preference of jassid (Amrasca bigutulla bigutulla Ishida) on eggplant (Solanum melongena L.) in Punjab Pakistan. Pak. Entomol., 38(1): 15-18.
Anwar, S., J.M. Mari, F. Ullah, M.A. Khanzada, H. Badshah, H. Zada and A. Ahmad. 2017. Population dynamics of brinjal shoot and fruit borer Leucinodes orbonalis Guen (Pyralidae: Lepidoptera) in central districts of Khyber Pakhtunkhwa, Pakistan. Pure Appl. Biol., 6(4): 1464-1476. https://doi.org/10.19045/bspab.2017.600158
Ashraf, H.M.I., M.W. Hassan and M. Jamil. 2017. Evaluation of Different Brinjal (Solanum melongena L.) Cultivars for Yield Performance and Sucking Insect Pests in Bahawalpur, Pakistan. J. Basic Appl. Sci., 13: 437-441. https://doi.org/10.6000/1927-5129.2017.13.72
Athawale, S., S. Suryawanshi and S. Gawande. 2023. Cost benefit analysis of brinjal cultivation in Amravati district of Maharashtra. Pharma Innov. J., 12(12): 2249-2254
Ayub, H.M.F., I.A. Khan, A. Sadozai, J. Sarwar and W. Ahmad. 2020. Population abundance and correlation of sucking insect pests and their natural enemies on different brinjal genotypes. Pure Appl. Biol., 9(1): 193-201. https://doi.org/10.19045/bspab.2020.90023
Barzman, M., P. Bàrberi, A.N.E. Birch, P. Boonekamp, S. Dachbrodt-Saaydeh, B. Graf and M. Sattin. 2015. Eight principles of integrated pest management. Agron. Sustain. Develop. 35(4): 1199-1215.
Bello, S.O., B.Y. Muhammad, K.S. Gammaniel, I. Abdu-Aguye, H. Ahmed, C.H. Njoku and A.M. Salka. 2005. Preliminary evaluation of the toxicity and some pharmacological properties of the aqueous crude extract of Solanum melongena. Res. J. Agric. Biol. Sci., 1(1): 1-9.
Bhatti, K.H.K., R. Nazia, H. Umer, N. Khalid and E.H. Siddiqi. 2013. Effects of biotic stresses on eggplant (Solanum melongena L.). World Appl. Sci. J., 26: 302–311.
Challa, N., M. Singh, R.K. Bharadwaj, R. Sharma, M.B. Gaikwad and P. Thakur. 2021. Characterization of eggplant genotypes for different resistance mechanisms against Leucinodes orbonalis. Neotrop. Entomol., 50: 643–653. https://doi.org/10.1007/s13744-021-00888-w
Chand, P., S.K. Mandal, A.P. Tiwari, A. Mishra and S.K. Yadav. 2024. Soil application of Cyazypyr 20% SC for jassid (Empoasca flavescens Ishida) control in brinjal. J. Exp. Agric. Int., 46(5): 474–478. https://doi.org/10.9734/jeai/2024/v46i52399
Chaudhary, S., R.K. Kanwar, A. Sehgal, D.M. Cahill, C.J. Barrow, R. Sehgal and J.R. Kanwar. 2017. Progress on Azadirachta indica based biopesticides in replacing synthetic toxic pesticides. Frontiers in Plant Sci., 8: Article 610. https://doi.org/10.3389/fpls.2017.00610
Choudhury, M.A.R., M.M. Rahman, M.Z. Alam, M.M. Hossain and Q.A. Khaliq. 2015. Fluctuation pattern of insect pests and natural enemies in summer brinjal ecosystem. J. Sylhet Agric. Uni., 2(2): 149-155.
Daunay, M.R., Lester and G. Ano. 2001. Cultivated eggplants, in Tropical Plant Breeding, A. Charpier, M. Jacquot, S. Hamon and D Nicolas, Eds., Oxford University Press, Oxford, UK.
Dhandapani, N., U.R. Shelkar and M. Murugan. 2003. Bio-intensive pest management in major vegetable crops. An Indian Perspective. J. Food Agri. Environ., 1(2): 330-339.
Dar, S.A., A.R. Wani, Muneer, A. Sofi and S.S. Pathana. 2017. IPM for brinjal shoot and fruit borer (Leucinodes Orbonalis)- A review. Ind. J. Entomol., 79(2): 130-137. https://doi.org/10.5958/0974-8172.2017.00027.X
Deguine, J.P., J.N. Aubertot, R.J. Flor, F. Lescourret, K.A. Wyckhuys and A. Ratnadass. 2021. Integrated pest management: good intentions, hard realities. A review. Agron. Sustain. Develop., 41(3): 38. https://doi.org/10.1007/s13593-021-00689-w
Dwarka., N. Chadar, S. Thakur, S. Parveen, S. Parmar, Maneesha and M.K. Ahirwar. 2024. Overview of Brinjal (Solanum melongena L.) Pests and Their Management: A Review. Arch. Curr. Res. Int., 24(11): 244-252. https://doi.org/10.9734/acri/2024/v24i11966
Elanchezhyan, K., R.K. Baskaran and D.S. Rajavel. 2008. Field screening of brinjal cultivars on major pests and their natural enemies. J. Biopest., 1(2): 113-120. https://doi.org/10.57182/jbiopestic.1.2.113-120
FAO FAOSTAT. Eggplant statistics. 2010. Statistical Division, Food and Agriculture Organization of the United Nations, 2012.
FAO, 2024. Statistical Yearbook, World Food and Agriculture. http://www.fao.org.)
Farooq, F. and I.R. Delvadiya. 2023. Blossoming heterosis: unveiling the potential of hybridization in eggplant (Solanum melongena L.). Int. J. Plant Soil Sci., 35(18): 2162-2168. https://doi.org/10.9734/ijpss/2023/v35i183530
Gautam, M., S. Kafle, B. Regmi, G. Thapa and S. Paudel. 2019. Management of brinjal fruit and shoot borer (Leucinodes orbonalis Guenee) in Nepal”. Acta Sci. Agric., 3(9): 188-195. https://doi.org/10.31080/ASAG.2019.03.0632
Gogoi, S., N. Mazumder and J. Talukdar. 2018. Evaluation of brinjal varieties for yield, genetic variability and disease reaction grown as late rabi season crop in Assam. Ind. J. Agric. Res., 52(2): 191-194. https://doi.org/10.18805/IJARe.A-4792
GoP. 2018. Fruit, vegetables and condiments statistics of Pakistan (2017-18). Minist. Nat. Food Secur. Res. http://www.mnfsr.gov.pk/frmDetails.aspx
Gulati, R. and M. Jangra. 2017. Incidence of Tetranychus urticae Koch on brinjal under field and screen house conditions. Emer. Life Sci. Res., 3: 16-22.
Habib, K., I.A. Khan, R. Akbar, A. Khan, M. Saeed, A. Farid, I. Ali and M. Alam. 2015. Response of Brinjal, Solanum melongena L. (Solanales: Solanaceae), Genotypes against Insect Pests in Peshawar. Pak. J. Entomol. Zool. Stud., 3(3): 423-427.
Halder, J., S. Majumder and K.K. Pandey. 2023. Whether the addition of neem oil increases the bioefficacy of entomopathogenic fungi against sucking pests: A case study from eggplant ecosystem. Munis Entomol. Zool., 18(1): 409–417.
Hassan, I., S.A. Jatoi, M. Arif and S.U. Siddiqui. 2015. Genetic variability in eggplant for agro-morphological traits. Sci. Technol. Develop., 34(1): 35-40. https://doi.org/10.3923/std.2015.35.40
Hrynko, I., B. Łozowicka and P. Kaczyński. 2021. Development of precise micro analytical tool to identify potential insecticide hazards to bees in guttation fluid using LC–ESI–MS/MS. Chemosph., 263: 128143. https://doi.org/10.1016/j.chemosphere.2020.128143
Jabeen, N., A. Javaid, A. Shoaib and I.H. Khan. 2021. Management of southern blight of bell pepper by soil amendment with dry biomass of Datura metel. J. Plant Pathol., 103(3): 901-913. https://doi.org/10.1007/s42161-021-00874-6
Javaid, A., F.A. Chaudhury, I.H. Khan and M.F.H. Ferdosi. 2022. Potential health-related phytoconstituents in leaves of Chenopodium quinoa. Advanc. Life Sci. 9(4): 574-578. https://doi.org/10.62940/als.v9i4.1552
Jalal-ud-Din, M. 2011. The socio-economic problems of small farmers in adopting new agricultural technology: A case study of three villages in District Mardan. Sar. J. Agric., 27(2): 299-304.
Javed, H., S.S. Hussain, K. Javed, T. Mukhtar and N.A. Abbasi. 2017. Comparative infestation of brinjal stem borer (Euzophera perticella) on six aubergine cultivars and correlation with some morphological characters. Pak. J. Agric. Sci., 54(4): 753-758.
Kantharajha, A. and P. Golegaonkar. 2004. Somatic embryogenesis in eggplant. Sci. Hort., 99(2): 107-117. https://doi.org/10.1016/S0304-4238(03)00090-6
Kaushik, P., J. Prohens, S. Vilanova, P. Gramazio and M. Plazas. 2016. Phenotyping of eggplant wild relatives and interspecific hybrids with conventional and phenomics descriptors provides insight for their potential utilization in breeding. Frontiers Plant Sci., 7: 677. https://doi.org/10.3389/fpls.2016.00677
Khan, I.A., K. Habib, R. Akbar, A. Khan, A. Saeed, A. Farid, I. Ali and M. Alam. 2015. Proximate chemical composition of brinjal, Solanum melongena L. (Solanales: Solanaceae), genotypes and its Correlation with the insect pests in Peshawar. J. Entomol. Zool. Stud., 3(4): 303-306.
Khan, M.M., Khan, M.Y., Ullah, R.M.K., Yasir, M., Khalid, A., & Khan, M.A. 2018. Morphological and biochemical characters of eggplant (Solanum melongena) conferring resistance against whitefly (Bemisia tabaci). J. Entomol. Zool. Stud., 6(5): 915-920.
Khan, I.H. and A. Javaid. 2021. Identification of biologically important compounds in neem leaves through GC-MS analysis. Jord. J. Pharmaceut. Sci., 14(3): 359-366.
Kundu, P.K., S. Parveen, M.S.A. Banu, M.H. Rashid and K.M.K. Huda. 2023. Morphological variations in some brinjal (Solanum melongena L.) genotypes. Bangladesh J. Agric., 48(1): 123-129. https://doi.org/10.3329/bjagri.v48i1.66763
Kumari, P., P. Jasrotia, D. Kumar, P.L. Kashyap, S. Kumar, C.N. Mishra, S. Kumar and G.P. Singh. 2022. Biotechnological Approaches for Host Plant Resistance to Insect Pests. Front. Genet., 13: 914029. https://doi.org/10.3389/fgene.2022.914029
Mabberley, D.J. 2008. Mabberley’s Plant-Book: A Portable Dictionary of Plants, their Classifcations and Uses, Cambridge University Press, Cambridge, UK.
Mahmood, T., S.I. Hussain, K.M. Khokhar, Hidayatullah and G. Jeelani. 2002. Varietal resistance in eggplant to cotton jassid (Amrasca biguttula biguttula). Asi J. Pl. Sci., 1(4): 107-108. https://doi.org/10.3923/ajps.2002.107.108
Mani, M., N. Natarajan, R.D. Hegde and M.K. Tej. 2022. Host Plant Resistance to Insect Pests in Horticultural Crops. Trends Hort. Entomol., 335-386. https://doi.org/10.1007/978-981-19-0343-4_11
Maqsood, S., M.U. Shafi, A. Javaid, I.H. Khan, M. Ali and M.F. Ferdosi. 2023. Control of insect pests and yield improvement in brinjal by plant extracts. Int. J. Biol. Biotechnol., 20(2): 329-335.
Ministry of National Food Security and Research. 2022-23. Government of Pakistan. Fruit, vegetables and condiments statistics of Pakistan.
Mishra, S.L., P. Tripathy, G.S. Sahu, D. Lenka, M.K. Mishra, S.K. Tripathy, G.G. Padhiary, A. Mohanty and S. Das. 2023. Study of heterosis, combining ability and gene action in brinjal (Solanum melongena L.) landraces of Odisha. Elect. J. Plant Breed., 14(2): 572-583. https://doi.org/10.37992/2023.1402.068
Mouden, S., K.F. Sarmiento, G.L.K. Peter and A.L. Kirsten. 2017. Integrated pest management in western flower thrips: past, present and future. Pest Manage. Sci., 73: 813–822. https://doi.org/10.1002/ps.4531
Muhammad, W., H. Javed, M. Ahmad and T. Mukhtar. 2021. Economical impact of some selected cultural practices on population build-up of Leucinodes orbonalis in brinjal crop. Fresenius Environ. Bull., 30: 7346-7354.
Muthukumar, M. and M. Kalyanasundaram. 2003. Efficacy of certain insecticides against major sucking insects of brinjal (Solanum melongena L.). South Ind. Hort., 51(6): 207-213.
Patel, H.V., G.G. Radadia and S.K. Chavda. 2015. Seasonal incidence of major insect pests of brinjal crop during summer season. Insect. Environ., 20(4): 149-151.
Prasad, B., D.B.L. Jat, P. Sharma, V. Kumar, V. Kumar and B. Singh. 2017. To assess the crop losses due to shoot and fruit borer, Leucinodes orbonalis Guenee.in brinjal. J. Entomol. Zool. Stud., 5(4): 826-828.
Prohens, J., M. Blanca and F. Nuez. 2005. Morphological and molecular variation in a collection of eggplants from a secondary center of diversity: implications for conservation and breeding, J. American Soci. Hort. Sci., 130(1): 54–63. https://doi.org/10.21273/JASHS.130.1.54
Rai, A.B., J. Halder and M.H. Kodandaram. 2014. Emerging insect pest problems in vegetable crops and their management: An appraisal. Pest Manag. Hort. Ecosys., 20(2): 113-122.
Raina, J. and G.S. Yadav. 2018. BSFB: Bioecology and management. J. Pharmacogn. Phytochem., 7(4): 444-449.
Rehman, S., I.A. Hafiz, I. Ali and N.A. Abbasi. 2019. Growth and Yield Response of Different Brinjal Cultivars to Irrigation Deficit Conditions. J. Hort. Sci. Technol., 2(3): 78-84. https://doi.org/10.46653/jhst190203078
Saeed, H.M., M.F.H. Ferdosi, I.H. Khan, A. Javaid and M.W. Sultan. 2023. Antibacterial activity and GCMS analysis of white flowers extract of Nerium oleander L., Int. J. Biol. and Biotechnol., 20(1): 163-168.
Sahito, H.A., F. Soomro, T. Kousar, Z.H. Shah and W.M. Mangrio. 2018. Population management of cotton jassid, Amrasca biguttula biguttula Ishida through its biological control agent, Arescon enocki (Rao and Kaur) under field and laboratory conditions at upper Sindh, Pakistan. Int. J. Biosci., 13(2): 210-216.
Sahu, P., M. Mandloi, and R.K. Jaiswal. 2022. Evaluation of different varieties of brinjal (Solanum melongena L.) For growth, yield and economics attributing characters. Pharma Innov. J., 11(1): 107-111.
Sahu, A. Dwarka and R. Pachori. 2023. The evaluation of insecticides against Leucinodes orbonalis on brinjal (Solanum melongena) crop. Zool. Entomol. Letter., 3(1): 37-42.
Sekara, A., S. Cebula and E. Kunicki. 2007. Cultivated eggplants–origin, breeding objectives and genetic resources, A review. Folia Hort., 19(1): 97–114.
Shah, A.N., E.E. Kandil, N. Manzoor, M. Islam, I. Afzal, C. Pinghua and C. Pinghua. 2023. Recent Advances on Nitrogen Use Efficiency in Crop Plants and Climatic Challenges. Front. Plant Sci., 184061.
Shaukat, M.A., A. Ahmad, F. Mustafa. 2018. Evaluation of resistance in brinjal (Solanum melongena L.) against brinjal shoot and fruit borer (Leucinodes orbonalis Guen.) infestation: A review. Int. J. Appl. Sci. Biotechnol., 6(3): 199-206. https://doi.org/10.3126/ijasbt.v6i3.19187
Singh, S. 2018. Agrometeorological requirements for sustainable vegetable crops production. J. Food Prot., 2(3): 1-22.
Steel, R. G. D and J. H. Torrie. 1980. Principals and procedures of the statistics. (With special reference to biological sciences). 2nd Edition. McGraw Hill Book Company New York. 4(3): 481.
Srinivasan, R. 2009. Insect and mite pests on eggplant: a field guide for identification and management. P. 64. In AVRDC–The World Vegetable Center, Shanhua, Taiwan. AVRDC.
Suroowan, S., K.B. Pynee and M.F. Mahomoodally. 2019. A comprehensive review of ethnopharmacologically important medicinal plant species from Mauritius. South African J. Bot., 122(1): 189-213. https://doi.org/10.1016/j.sajb.2019.03.024
Thakar, P.K., P.S. Patel, R.S. Jaiman and S. Deb. 2024. Harnessing Natural Arsenal for Effective Management of Jassid on Brinjal (Solenum melongena L.). J. Exp. Agric. Int., 46(11): 655-662. https://doi.org/10.9734/jeai/2024/v46i113087
Thapa, R. B. 2010. Integrated management of brinjal fruit and shoot borer, Leucinodes orbonalis Guenee: An overview. J. Ins. Agric. Ani. Sci., 30(32): 1-16.
Ullah, S., U. Ijaz, T.I. Shah, M. Najeebullah and S. Niaz. 2014. Association and genetic assessment in brinjal. Euro. J. Biotech. Biosci., 2(5): 41–45.
Ullah, M., F. Ullah, M.A. Khan, S. Ahmad, M. Jamil, S. Sardar and N. Ahmed. 2022. Efficacy of various natural plant extracts and the synthetic insecticide cypermethrin 25EC against Leucinodes orbonalis and their impact on natural enemies in brinjal crop. Int. J. Trop. Insect Sci., 42: 173-182. https://doi.org/10.1007/s42690-021-00528-1
Younas, Z., S. Naseer, A. Kazmi, A. Ali, A. Wahab, T. Sultana and M. Rahimi. 2022. Assessment of diversity among important Brinjal (Solanum melongena) cultivars using morphological markers. J. Food Quality., (1):1-13. https://doi.org/10.1155/2022/4255554
Yousafi, Q., M. Afzal, M. Aslam, M. Razaq and M. Shahid. 2013. Screening of Brinjal (Solanum melongena L.) Cultivars Sown in autumn for Resistance to Cotton Jassid Amrasca biguttula biguttula (Ishida). Pak. J. Zool., 45(4): 897-902.
Yousafi, Q., M. Afzal, M. Aslam and A.D. Abid. 2016. Effectiveness and benefit cost ratio of selected insecticides at different application on intervals for brinjal shoot and fruit borer, Leucinodes orbonalis (G.) management on brinjal, Solanum melongena (L.) at Sahiwal, Pakistan. Phytoparas., 44: 423-427. https://doi.org/10.1007/s12600-016-0527-0
Yousafi, Q., M. Aslam and S. Saleem. 2020. Varietal Screening of Brinjal against Aphid (Aphis gossypii G.) Infestation and Population Fluctuation Plus Interaction between Aphid and Ladybeetle (Coccinella septempunctata L.) Populations. Pak. J. Zool., 52(1): 223. https://doi.org/10.17582/journal.pjz/2020.52.1.223.230