An important vegetable in Ethiopia is cabbage (Brassica oleracea L. var. capitata), but the cabbage aphid severely limits its production, resulting in yield losses of up to 80%. Reliance on synthetic insecticides has created environmental and health risks, suggesting that there must be underscoring sustainable pest control alternatives. This study assessed the efficacy of botanicals (Endod, Tobacco, Tinju, and Kitkita) against cabbage aphids in the Koga Irrigation Scheme during the 2023 irrigation season. The experiment used a randomized full block design with three replications and fourteen treatments, including three concentration levels for each botanical, a chemical check (Dimethoate 40% EC), and a control. SAS 9.4 software examined data on aphid infestation, efficacy, plant growth, yield, and economic return. All botanical treatments significantly suppressed aphid populations compared with the control. The highest efficacy was recorded in Endod 7.5% (87.17%) and Tobacco 7.5% (82.12%), comparable to Dimethoate 40% EC (92.76%). Moreover, Endod 7.5% yielded the largest net benefit (762,138 ETB ha⁻¹) with a benefit–cost ratio of 6.69, the lowest yield loss (3.49%), and the highest marketable yield (49.78 t ha⁻¹). Increasing concentration and repeated applications enhanced performance. Therefore, Endod extract at 5–7.5% concentration is recommended as an effective, economical, and eco-friendly botanical option for sustainable cabbage aphid management in Ethiopia.
INTRODUCTION
Cabbage (Brassica oleracea L. var. capitata) is one of the most popular food crops cultivated throughout the world. Brassica leafy vegetables are widely cultivated in Africa, including Ethiopia. In Ethiopia, head cabbage is mostly produced for consumption and as a source of income (Tekle & Tesfu, 2023).
In contrast to other major cabbage-producing nations, Ethiopia in general and Amhara Regional State in particular have very low levels of cabbage production and productivity (Habtamu & Mnuyelet, 2022). In 2018, Ethiopia produces only 6 tons of cabbage per hectare, which is much less than the 16 tons produced in East Africa and the 28.8 tons produced worldwide (CSA, 2021).
The quantity and quality of cabbage are influenced by various factors. Aphids are, the most economically important insect pests of cabbage. Aphids spread 50% of all insect-borne plant viruses in addition to their feeding influence (Gebreyohans, 2021). Cabbage aphid had the potential to lower cabbage yields, quality, and nutritional value (Opfer & McGrath, 2013). According to Lidet et al. (2008), entire crop failures were common during seasons with significant infestations, and losses varied from 36.1 to 91.2%. The production of cabbage has become risky, which may have an impact on the quality and market value in Ethiopia (Shiberu & Mulugeta, 2016). As Kassahun (2018) reported, the cabbage aphid is a significant pest that causes a 50–80% production reduction in the Amhara Region, Ethiopia (Abdelmuhsin et al., 2022; Fiodorova et al., 2022; Zakinyan et al., 2023; Negreiros et al., 2024).
The use of synthetic insecticides is critical for controlling cabbage aphids and increasing crop productivity (Iqbal et al., 2011). Chemical pesticides are still employed by cabbage-grower farmers to control aphids (Mengistie et al., 2017). Persistent use of chemical pesticides creates a multitude of negative results, including resistance, residues in harvested product, injury to farmers, beneficial insects, and non-target creatures, contamination of the environment, and financial loss (Shiberu & Mulugeta, 2016). Knowing the negative effects of synthetic chemicals allows for the implementation of alternate control strategies, including using botanicals to reduce synthetic chemical-related problems (Mahmood et al., 2022). It is well known that botanicals, or plant-based pesticides, have insecticidal and repellent qualities as well as reduced environmental toxicity (Zahid et al., 2016). Therefore, the purpose of this study was to assess the effectiveness of botanical aqueous extracts in controlling cabbage aphids in field settings.
MATERIALS AND METHODS
Description of the study area
The study was conducted at the Koga Irrigation Scheme in North Mecha District during the irrigation season of 2023. It is located at11° 23' 62'' N latitude and 37° 07' 87'' E longitude with an average elevation of 1850 meters above sea level. The mean annual rainfall is 1480 mm. The monthly mean temperature is 25.8°C. The soil at the experiment site is categorized as clay in its textural classification, with a pH value of 5.32. The major crops grown in the study area are Wheat, Barely, Maize, Beans, Cabbage, Potatoes, Tomatoes, Onions, Shallots, and peppers.
Collection and extraction of botanicals
The matured Endod, Kitkita, and fresh and mature Tinjut leaves were harvested in the North Mecha District, whilst tobacco leaves were taken in the Dengur District near Metekel. The leaves were washed, sanitized, and dried in the shade for 15 days to reduce chemical volatility and provide enough air supply (Sarwar, 2015). The dried leaves were cut into small bits to make them easier to grind. The dried leaves are pulverized using a mortar and pestle. Ground leaves of each measured Endod, Tobacco, and Tinjut leaf powder at 2.5%, 5%, and 7.5%, and Kitkita powder at 7.5%, 10%, and 12.5% were diluted with one liter of distilled water. The combinations were thoroughly mixed with frequent agitation at 3-hour intervals for one day to release their toxicity. After one day, the mixed mixture was filtered with cheesecloth for field spraying, and the leaves' aqueous extract stock solutions were diluted and treated at a rate of 150 liters per hectare (Alula & Tesfaye, 2021), with 0.09 liters per plot administered using a hand sprayer. Five superiors were performed at weekly intervals when the plants were at the 6-8 true leaf stage.
Description of experimental materials, treatment, and design
The cabbage variety “Copenhagen Market” was used to raise seedlings of the test crop. This variety grows well at altitudes from 500 to 3000 meters above sea level with a rainfall requirement of 380-550 mm. It can reach maturity in 90-110 days and provides 3-4 t/ha (MoA, 2019). The experiment consisted of 14 treatments. It includes four botanicals, namely, tobacco (Nicotiana tabacum L.) leaves, endod (Phytolacca dodecandra) leaves, tinjut (Otostegia integrifolia (Benth)) leaves with a concentration of 2.5%, 5%, and 7.5%, and kitikita (Dodonaea angustifolia) leaves with a concentration of 7.5%, 10%, and 12.5%. A standard check of dimethoate 40% EC (1.5 L/ha) (FAO & WHO, 2022) and an untreated check were used. The experiment was laid out in a Randomized Complete Block Design (RCBD) with three replications. The treatments were randomly assigned to the unit plot of 2.50 m x 2.40 m = 6 m². The experimental area was divided into three blocks. The total area of the experimental plot was 428.4 m². The net size of the main plot was 252 m². The blocks and plots were spaced at 1.5 m² and 0.5 m², respectively. Seedlings were planted 30 cm between plants and 50 cm between rows (Aklilu, 2019). There were five rows per plot and eight plants per row, with a total of 40 plants per plot planted.
Experimental procedures and management
Cabbage seeds were sown on a 5 m² raised seedbed in 10 cm rows, covered with mulch and soil. Mulch was removed upon germination. Seedlings were irrigated twice daily initially, then reduced after a week, and watering was stopped a week before transplanting to harden the seedlings (MoA, 2019). After five weeks, healthy seedlings with 3–4 true leaves were transplanted. DAP (100 kg/ha) and urea (200 kg/ha) were applied, with DAP at transplanting and urea split equally—half applied one month after transplanting and the remainder at the start of head formation (MoA, 2019).
Data collection
Data were collected before and after three days of treatment application. Data collection was carried out from two weeks after seedling transplantation up to harvest. The experimental plot contains five rows, and the data is obtained from the three central rows. Six plants were sampled randomly, and information on the parameters of the cabbage aphid infestation was gathered. The cabbage yield production was finally calculated and reported in tons per hectare.
Infestation percentage
Before each interval between treatments, the number of afflicted plants was counted, noted, and converted to a percentage using the Abbott (1925) methodology:
|
I |
(1) |
The numbers were recorded randomly at the middle of three central rows. Six plants per plot were sampled. The numbers of aphids were recorded before the spray and 72 hours after the application of botanicals or chemicals at weekly intervals. The numbers of aphids tagged on leaves were counted with the help of a hand lens. The number of aphids per plant was recorded. The efficacy of each treatment was calculated using the efficacy percentage formula (Abbott, 1925).
|
|
(2) |
This is the number of the plant stand at crop establishment. The number of plants in each plot was counted to determine the stand count both at harvest and during crop setup. Plant stand reduction was determined by subtracting the stand count during seedling establishment from the stand count at harvest.
|
|
(3) |
Where Yp = the yield of maximum protected plot
Yt= yield from plots of other treatments
Data and partial budget analysis
SAS version 9.4 was utilized to analyze the results of the experiment. To determine the average impacts of botanicals and chemicals on aphid fatalities, effectiveness % was computed and then subjected to an analysis of variance (ANOVA). DMRT (Duncan's Multiple Range Tests) was used to calculate means separation utilizing statistical software (P < 0.05). Additionally, analysis of variance (ANOVA) was performed on the mean value of the recorded agronomic information. The significant distinction technique was used to determine mean separation if there were significant differences between the treatments.
The cost-benefit analysis of each treatment application was conducted using the basic partial budget approach described by CIMMYT (1988). A measure of the impact of new capital invested on net returns under new management as opposed to the previous one is the marginal rate of return, expressed as tons per hectare, which was calculated (AlHussain et al., 2022; Kumar et al., 2022; Spirito et al., 2022; Hackenberg et al., 2023; Prada et al., 2024).
|
|
(4) |
Gross benefit was computed by multiplying Adjusted yield with the current market prices
|
Gross Benefit=Adjusted Yield*Market price |
(5) |
For each therapy, the net benefit was determined by deducting the total expenditures from the gross field benefit.
|
ETB/ha net profit = Gross Benefit - Total variable Cost |
(6) |
Total cost: The price of materials, applications, labor, and chemicals are all included.
The benefit-cost ratio (BCR) was also determined as:
|
|
(7) |
RESULTS AND DISCUSSION
Effect of botanical extracts application on cabbage aphid infestation
The effect of botanical extract concentration on cabbage aphid infestation was highly significant (P<0.001) (Table 1). One week after transplanting, aphid infestation declined in all botanical treated plots but increased in the control. The lowest infestations were recorded with Endod 7.5% (17.56%) and tobacco 7.5% (18.44%), following the standard check, Dimethoate 40% EC (15.11%), while the control showed 33.22%. By the third week, infestation further decreased in Endod 7.5% (9.11%), Endod 5% (9.89%), and tobacco 7.5% (9.94%) treatments, next to Dimethoate (5.17%), but rose in the control (68.8%). In the fourth week, infestation peaked in the untreated plot (83.67%) and was lowest in Dimethoate (4.61%) and Endod 7.5% (6.06%). By the fifth week, infestation dropped significantly in Endod 7.5% (5.44%) and 5% (5.89%) compared to Dimethoate (3.89%), while the control reached 99.88%. Overall, higher botanical concentrations consistently reduced aphid infestation, while untreated plots showed continuous increases. Endod 7.5% performed comparably to the standard chemical check, Dimethoate 40 EC.
These findings agree with earlier studies (Begna, 2014; Desale & Getnet, 2018; Kassahun, 2018; Mulu et al., 2023), confirming that increasing botanical concentration enhances aphid control. Desale and Getnet (2018) found that Tinjut leaves at different concentrations decreased the infestation level of cabbage aphids as the Tinjut concentration increased. Kassahun (2018) studied the management of cabbage aphids by using tobacco leaf extract in different concentrations and indicated that the infestation level of cabbage aphids decreased when tobacco concentration increased. Begna (2014) also found that cabbage aphids treated with botanicals such as Phytolacca dodecandra L'Herit, garlic, neem, and, chili recorded a higher infestation level than the conventional pesticides. The onion cultivars treated with botanical neem had the highest death rate and the fewest onion thrips (Mulu et al., 2023).
Table 1. Effect of different concentrations of botanicals on aphid infestation on Cabbage
|
Treatment |
Concentration% |
BT infestation |
2nd week infestation |
3rd week infestation |
4th week infestation |
5th week infestation |
|
Endod |
2.5 |
26.22 |
19.11efd |
10.11e |
7.56fe |
6.83gf |
|
Endod |
5 |
26.33 |
18.44gf |
9.89fe |
6.78fg |
5.89gh |
|
Endod |
7.5 |
26.22 |
17.56g |
9.11f |
6.06g |
5.44h |
|
Kitkita |
7.5 |
26.39 |
21.11b |
14.94b |
14.06a |
10.88b |
|
Kitkita |
10 |
25.89 |
20.89cb |
14.78cb |
13.44cb |
9.89cb |
|
Kitkita |
12.5 |
26.33 |
20.78cb |
14.67cb |
13.28cb |
9.22cd |
|
Tobacco |
2.5 |
26.16 |
20.00f |
11.44d |
8.11e |
7.61ef |
|
Tobacco |
5 |
26.33 |
19.00efd |
10.06e |
7.11f |
6.94gf |
|
Tobacco |
7.5 |
26.22 |
18.78ef |
9.94fe |
6.94f |
6.83gf |
|
Tinjut |
2.5 |
25.29 |
20.56cb |
14.50cb |
12.89cb |
9.06cd |
|
Tinjut |
5 |
26.33 |
20.22cbd |
14.00c |
12.44d |
8.67ed |
|
Tinjut |
7.5 |
26.22 |
19.78ced |
13.89c |
12.11d |
7.28f |
|
Dimethoate40EC |
1.5l/ha |
23.67 |
15.11h |
5.17g |
4.61h |
3.89i |
|
Untreated |
|
26.06 |
33.22a |
68.72a |
83.67a |
99.83a |
|
SE (±) |
|
1.09 |
0.69 |
0.49 |
0.45 |
0.63 |
|
Mean |
|
25.94 |
20.34 |
15.80 |
14.93 |
14.16 |
|
CV (%) |
|
4.23 |
3.37 |
3.13 |
3.01 |
4.46 |
|
P>F |
|
0.46 |
* |
* |
* |
* |
BT= Before treatment; Means in the same letter within a column are not significantly different
Efficacy of botanicals on the management of cabbage aphids
The number of cabbage aphids per plot was significantly influenced by botanical extract concentrations (P < 0.001) (Table 2). Aphid populations declined progressively in all botanical treatments after each spray, while they continued to rise in the untreated control plots.
After the first treatment (72 hours post-application), all botanicals reduced aphid numbers, whereas the control showed an increase. Endod extract at 7.5% and 5%, and tobacco extract at 7.5%, were most effective, reducing infestations by 46.51%, 44.83%, and 43.29%, respectively, next to the standard Dimethoate 40% EC. Kitkita 7.5% showed the lowest efficacy (16.59%) (Table 2).
Following the second treatment, Endod 7.5% achieved the highest reduction (76.32%), followed by Dimethoate (58.73%), while Kitkita 7.5% again showed minimal effect (18.33%). After the third application, Endod 7.5%, Endod 5%, and tobacco 7.5% recorded 66.49%, 63.32%, and 61.12% reductions, respectively, compared with Dimethoate (85.6%). Similar trends were observed after the fourth spray, and by the fifth week, Endod 7.5% reached 87.17% reduction, close to Dimethoate (92.76%), whereas Kitkita 7.5% had only 21.71%.
Across all intervals, botanical treatments substantially suppressed aphid populations, confirming that their efficacy was concentration-dependent. Aphid density increased only in the control plots. These results agree with Isman (2000), who noted reduced aphid feeding with higher botanical concentrations, and Kapoor and Sharma (2020), who attributed this to bioactive insecticidal compounds.
Comparable studies support these findings. Gonfa and Shiberu (2022) reported that tobacco extracts effectively killed Brevicoryne brassicae nymphs and adults. Alula and Tesfaye (2021) observed that Endod 5% and Kitkita 10% reduced aphids by 84% and 22.33%, respectively, consistent with the present results (81.72% and 22.41%). Kitkita generally performed poorly under field conditions, as also reported by Shiberu and Mulugeta (2016). Endod efficacy increased with concentration, achieving 87.17% reduction at 7.5%, aligning with Megersa (2016), who recorded 100% mortality at 10%.
In the current study, botanicals reduced aphid populations below the economic threshold by the third application and nearly eradicated them after the fifth spray. This strong suppression likely resulted from both toxic and repellent effects and the dispersal of winged aphids from treated plots, similar to observations by Megersa (2016).
Other studies also confirm concentration-dependent performance: Desale and Getnet (2018) for Tinjut extract, Kassahun (2018) and Patel et al. (2024) for tobacco (62.73% mortality at 5%), and Kumar and Tayde (2019), who observed a 69.68% reduction. Lanjar et al. (2017) also reported that tobacco varieties effectively suppressed cabbage aphids. Tesfaye et al. (2021) demonstrated neem’s strong efficacy, while Chane and Jenber (2025) found Endod seed extract comparable to Malathion 5% dust in insect mortality. Overall, Endod and tobacco leaf extracts, particularly at 7.5%, were the most effective botanicals for managing cabbage aphids under field conditions, showing strong potential as eco-friendly alternatives to synthetic insecticides.
Table 2. Efficacy of botanicals for the management of cabbage aphids on Cabbage
|
Treatment |
Concentration% |
1st week efficacy |
2nd week efficacy |
3rd week efficacy |
4th week efficacy |
5th week efficacy |
|
Endod |
2.5 |
42.61d |
50.87e |
58.31e |
70.19f |
71.33f |
|
Endod |
5 |
44.83c |
55.99c |
63.32c |
81.72c |
85.24c |
|
Endod |
7.5 |
46.51b |
58.73b |
66.49b |
86.26b |
87.17b |
|
Kitkita |
7.5 |
16.59i |
18.33j |
19.59j |
21.52l |
21.71m |
|
Kitkita |
10 |
18.06h |
19.23ji |
20.62ji |
22.41l |
23.32l |
|
Kitkita |
12.5 |
18.98h |
20.05i |
21.47i |
24.89k |
26.19k |
|
Tobacco |
2.5 |
40.68e |
46.70f |
56.04f |
68.35g |
69.22g |
|
Tobacco |
5 |
42.90d |
52.34d |
59.50e |
72.19e |
74.68e |
|
Tobacco |
7.5 |
43.29d |
53.53d |
61.12d |
74.45d |
77.31d |
|
Tinjut |
2.5 |
34.24g |
40.45h |
49.44h |
60.64j |
63.65j |
|
Tinjut |
5 |
35.43g |
43.17g |
51.86g |
64.18i |
65.19i |
|
Tinjut |
7.5 |
37.88f |
44.57g |
53.05g |
66.18h |
66.93h |
|
Dimethoate40EC |
1.5l/ha |
80.41a |
76.32a |
85.61a |
89.27a |
92.77a |
|
Control |
|
0.0000j |
0.0000k |
0.0000k |
0.0000m |
0.0000n |
|
SE (±) |
|
0.82 |
0.84 |
0.88 |
0.85 |
0.67 |
|
Mean |
|
35.89 |
41.45 |
47.60 |
57.29 |
58.91 |
|
CV (%) |
|
2.28 |
2.04 |
2.04 |
1.85 |
1.14 |
|
P>F |
|
* |
* |
* |
* |
* |
Means in the same letter within a column are not significantly different (p<0.05)
Effect of botanicals on stand count and cabbage head formation
Endod with concentrations of 5% and 7.5% (41.00 and 41.33) had the highest plant stand count when compared to the standard check Dimethoate 40EC (41.67) and control plots (31.67). The largest cabbage head production was found in Endod-treated plots with concentrations of 5% and 7.5%, which were 39.33 and 40.0, respectively, adjacent to the standard check Dimethoate 40EC (41.33) in comparison to the control plots (26.33). The medium stand count and cabbage head development were determined from cabbages treated with the remaining treatments. Relatively lower mean stand counts (35.00 and 35.33) and head formations (30.33 and 31.33) were recorded in Kitkita leaves with concentrations of 7.5% and 10% treated plots among botanicals close to the control. The highest stand count and head formation were seen in Endod at 5% and 7.5% doses (Table 3). It could have happened because it limits the number and potential of parasitic insects that feed on head cabbage plants. These findings corroborate Desale and Getnet's (2018) claim that the efficiency of a treatment that reduces the effects of cabbage aphids is the key factor of cabbage head development. This could mean that botanicals have a deterrent effect or are harmful antifeedants.
Table 3. Effect of botanicals on stand count, head formation, Plant height and Canopy Spread
|
Treatment |
Concentration% |
Stand count |
Head formation |
Plant height |
Canopy spread |
|
Endod |
2.5 |
39.33 bdc |
37.00de |
25.78bcd |
36.22d |
|
Endod |
5 |
41.00bac |
39.33bc |
27.39ba |
37.56c |
|
Endod |
7.5 |
41.33ba |
40.00ba |
27.89ba |
38.22b |
|
Kitkita |
7.5 |
35.00g |
30.33g |
22.28ef |
32.78h |
|
Kitikita |
10 |
35.33g |
31.33g |
22.67ef |
33.50g |
|
Kitikita |
12.5 |
36.00 fg |
32.00g |
22.89ef |
33.94g |
|
Tobacco |
2.5 |
39.00dc |
36.33def |
24.50ecd |
35.44e |
|
Tobacco |
5 |
39.67bdac |
37.33de |
26.00bcd |
36.33d |
|
Tobacco |
7.5 |
40.00bdac |
38.00dc |
26.44bc |
36.67d |
|
Tinjut |
2.5 |
36.67feg |
34.67f |
23.33e |
34.61f |
|
Tinjut |
5 |
38.00fde |
35.67ef |
23.500e |
35.06fe |
|
Tinjut |
7.5 |
38.67de |
36.00ef |
24.00ed |
35.33e |
|
Dimethoate40EC |
|
41.67a |
41.33a |
29.28a |
39.67a |
|
Control |
|
31.67h |
26.33h |
21.00f |
29.67i |
|
SE (±) |
|
1.18 |
1.04 |
1.17 |
0.27 |
|
Mean |
|
38.09 |
35.40 |
24.79 |
35.36 |
|
CV (%) |
|
3.11 |
2.94 |
4.72 |
1.77 |
|
P>F |
|
* |
* |
* |
* |
Means in the same letter within a column are not significantly different
Effect of botanicals on plant height and canopy spread
The effect of botanical extracts on the height and canopy spread of cabbage plants varied depending on the treatment (Table 3). Plots treated with Endod leaf extract at a 7.5% concentration showed the highest plant height and canopy spread, with mean values of 27.89 cm and 36.22 cm, respectively. These results were compared to the standard check, Dimethoate 40% EC, which showed 29.28 cm plant height and 38.17 cm canopy spread. Medium plant height and canopy spread were produced by cabbages treated with different botanical extracts at lower dosages.
Among the botanicals, relatively lower plant height and canopy spread were recorded in Kitkita leaf extract at 7.5% concentration (22.28 cm and 32.78 cm, respectively), followed by the untreated control, which showed the lowest plant height (21.00 cm) and canopy spread (29.67 cm).
This finding is consistent with those reported by Alula and Tesfaye (2021), who found no significant difference among treatments in cabbage plant height and canopy spread when treated with Endod leaf extract (5%) and Kitkita leaf extract (10%), recording 25.67 ± 4.73 cm and 38.67 ± 3.06 cm for Endod, and 26.67 ± 3.51 cm and 37.00 ± 10.58 cm for Kitkita, respectively. In the present study, the tallest plants and widest canopy spread were obtained from Endod-treated plots (5% and 7.5%), while the shortest plants and narrowest canopies were observed in the untreated control plots.
This outcome is consistent with Begna and Tebkew (2015), who found that plants treated with synthetic or botanical insecticides grew taller than untreated (control) plots. Similarly, Alula and Tesfaye (2021) reported comparable trends in plant growth performance, confirming that botanical insecticide applications particularly Endod, can promote healthier plant growth by effectively reducing pest pressure.
Cabbage total yield, marketable yield and unmarketable yield
The botanical concentration differential had a substantial effect on cabbage yield. The maximum yield was found in Endod berry treated plots with a 7.5% concentration compared to the standard control Dimethoate 40EC. The remaining treatments had medium yields. Lower cabbage yields were seen in plots treated with Kitikita. The highest unmarketable yield was seen on untreated plots (Table 4). These results are consistent with prior studies. According to Desale and Getnet (2018), the total marketable yield of Tinjut at concentrations of 2.5%, 5%, and 7.5% was 35.43, 36.87, and 49.64 tons per hectare, respectively.
At a 10% concentration, Kitikita had a total marketable output of 31.09 tons per hectare, while Endod had a total marketable yield of 48.02 tons per hectare. These results are consistent with recent findings (Alula & Tesfaye, 2021), which show that the total marketable yield of kitikita at a 10% concentration was 31.59 ton/ha and Endod 5% was 50.07 ton/ha. Tobacco's total marketable yield at 2.5, 5, and 7.5% concentrations was 44.39, 45.27, and 46.89 tons per hectare.
In this study, the highest level of yield was obtained in Endod within the concentration of 7.5% which was 49.78 ton/ha compared with Dimethoate 40EC (51.58 ton/ha). Plots treated with endod showed higher yields; this could be because it reduced the parasite bug that feeds on head cabbage plants, thereby reaching its maximum potential. In line with this, Sarwar (2015) determined that the extract from endod leaves performed better than the control and that sucking pests were eliminated. Thus, the crop's growth and yield were improved. In this study, the greatest Endod concentration produced the highest commercial yield. The control plots produced the lowest commercial yield. Bhat and Dhoj (2005), found that the control plots' marketable yield is significantly lower than that of the treated plots.
The difference in marketable yield was due to the aphicidal effect and concentration of botanical treatments. Cabbage aphids reduce yield directly by sucking sap and indirectly by producing honeydew that hinders photosynthesis, spreads viral diseases, and deforms heads. Higher botanical concentrations increased marketable yield, supporting Desale and Getnet (2018). Repeated application of concentrated extracts enhanced cabbage yield and quality by improving traits such as plant height, canopy spread, and head formation.
Table 4. Effect of botanicals on Cabbage yield, yield components and yield loss
|
Treatment |
Concentration |
Total Yield |
Marketable yield |
Unmartketable yield |
Yield loss |
|
Endod |
2.5 |
46.83fe |
45.11de |
1.72c |
12.55h |
|
Endod |
5 |
50.27bc |
48.02bc |
2.25cb |
6.91j |
|
Endod |
7.5 |
51.94ba |
49.78ba |
2.155cb |
3.49k |
|
Kitkita |
7.5 |
32.52i |
30.03i |
2.49cb |
41.78b |
|
Kitkita |
10 |
33.55i |
31.09ih |
2.46cb |
39.73c |
|
Kitkita |
12.5 |
37.12h |
34.34h |
2.78b |
35.64d |
|
Tobacco |
2.5 |
46.36fe |
44.39fe |
1.97cb |
13.95h |
|
Tobacco |
5 |
47.89de |
45.28de |
2.61cb |
12.22h |
|
Tobacco |
7.5 |
49.07dc |
46.89dc |
2.18cb |
9.09i |
|
Tinjut |
2.5 |
39.46g |
37.21g |
2.25cb |
27.87e |
|
Tinjut |
5 |
41.09g |
38.49g |
2.59cb |
25.38f |
|
Tinjut |
7.5 |
44.79f |
42.54f |
2.25cb |
17.52g |
|
Dimethoate40EC |
1.5l/ha |
53.09a |
51.58a |
1.51cb |
- |
|
Control |
|
20.91j |
16.17j |
4.74a |
68.65a |
|
SE (±) |
|
1.06 |
1.22 |
0.44 |
1.97 |
|
Mean |
|
42.49 |
40.07 |
2.43 |
22.48 |
|
CV (%) |
|
2.49 |
3.03 |
18.33 |
8.79 |
|
P>F |
|
* |
* |
* |
* |
Means in the same letter within a column are not significantly different
Yield loss
The biggest yield loss was found in Kitikita treated plots with a concentration of 7.5% (41.78%), followed by untreated check plots (68.65%). The medium yield reduction was observed in the remaining botanical concentrations. Lower cabbage yield losses were seen in Endod treated plots with a concentration of 7.5% (3.49%) compared to the standard check, Dimethoate 40% EC. According to this study, cabbage aphid produces a 68.65% yield reduction in the untreated check (Table 4). Botanicals reduce yield loss by disrupting aphid feeding behavior. This finding is consistent with Shonga and Emana's (2021) finding that cabbage aphid caused an 80% yield loss without treatment.
Partial budget analysis for the management of cabbage aphid using botanicals
The management cost of cabbage aphid control was calculated based on material, labor, and chemical expenses at current market prices. Cabbage yield (kg/ha) and revenue were estimated using a market price of 20 ETB/kg. Endod extract at 5% and 7.5% concentrations produced the highest net benefits (730,350.4 and 762,138.4 ETB/ha) (Table 5), benefit–cost ratios (6.45 and 6.69), and marginal rates of return (32.9 and 34.84) (Table 6). Tobacco extract at 7.5% yielded the second-highest net benefit (701,247.6 ETB/ha) with a benefit–cost ratio of 5.9 and a marginal rate of return of 20.5. Kitikita at 7.5% recorded the lowest economic return (403,305.1 ETB/ha; BCR 3.94; MRR 11.3). The lowest marginal return (9.6) was observed in Dimethoate 40EC due to its high cost. These findings agree with Alula and Tesfaye (2021), who reported higher profitability of Endod over chemical insecticides, and with Begna and Tebkew (2015), Jenber et al. (2024), Abaynew et al. (2020), and Yechale et al. (2021), who also confirmed that botanical treatments enhance net benefit and marginal return through cost-effective pest management.
Table 5. Partial budget analysis for the management of cabbage aphid using botanicals
|
Treatment |
Concentration% |
Adjusted yield (kg/ha) |
Total variable cost |
Growth benefit |
Net benefit |
|
Endod |
2.5 |
40599.9 |
161455.6 |
811998 |
650542.4 |
|
Endod |
5 |
43215.3 |
133955.6 |
864306 |
730350.4 |
|
Endod |
7.5 |
44804.7 |
133955.6 |
896094 |
762138.4 |
|
Kitkita |
7.5 |
27029.7 |
137288.9 |
540594 |
403305.1 |
|
Kitikita |
10 |
27980.1 |
137288.9 |
559602 |
422313.1 |
|
Kitikita |
12.5 |
29880 |
137288.9 |
597600 |
460311.1 |
|
Tobacco |
2.5 |
39954.6 |
140900 |
799092 |
658192.0 |
|
Tobacco |
5 |
40750.2 |
142011.1 |
815004 |
672992.9 |
|
Tobacco |
7.5 |
42204.6 |
142844.4 |
844092 |
701247.6 |
|
Tinjut |
2.5 |
33485.4 |
135622.2 |
669708 |
534085.8 |
|
Tinjut |
5 |
34640.1 |
137566.7 |
692802 |
555235.3 |
|
Tinjut |
7.5 |
38289.6 |
139511.1 |
765792 |
626280.9 |
|
Dimethoate40EC |
- |
46424.7 |
177011.1 |
928494 |
751482.9 |
|
Control |
- |
14554.8 |
117077.8 |
291096 |
174018.2 |
Table 6. Dominance analysis, benefit cost ratio and marginal rate of return for the management of cabbage aphid using botanicals
|
Treatment |
Concentr |
AY |
TVC/HA |
GB |
NB |
DA |
BCR |
MRR |
|
Control |
* |
14554.8 |
117077.8 |
291096 |
174018.2 |
~ |
2.49 |
* |
|
Endod |
5 |
43215.3 |
133955.6 |
864306 |
730350.4 |
|
6.45 |
32.9 |
|
Endod |
7.5 |
44804.7 |
133955.6 |
896094 |
762138.4 |
|
6.69 |
34.8 |
|
Tinjut |
2.5 |
33485.4 |
135622.2 |
669708 |
534085.8 |
D |
4.94 |
18.6 |
|
Kitkita |
7.5 |
27029.7 |
137288.9 |
540594 |
403305.1 |
D |
3.94 |
11.3 |
|
Kitikita |
10 |
27980.1 |
137288.9 |
559602 |
422313.1 |
D |
4.08 |
12.3 |
|
Kitikita |
12.5 |
29880 |
137288.9 |
597600 |
460311.1 |
D |
4.35 |
14.2 |
|
Tinjut |
5 |
34640.1 |
137566.7 |
692802 |
555235.3 |
D |
5.04 |
19.4 |
|
Tinjut |
7.5 |
38289.6 |
139511.1 |
765792 |
626280.9 |
D |
5.49 |
20.2 |
|
Tobacco |
2.5 |
39954.6 |
140900 |
799092 |
658192 |
D |
5.67 |
20.3 |
|
Tobacco |
5 |
40750.2 |
142011.1 |
815004 |
672992.9 |
D |
5.73 |
20.0 |
|
Tobacco |
7.5 |
42204.6 |
142844.4 |
844092 |
701247.6 |
D |
5.91 |
20.5 |
|
Endod |
2.5 |
40599.9 |
161455.6 |
811998 |
650542.4 |
D |
5.02 |
29.8 |
|
Dimethoate40EC |
|
46424.7 |
177011.1 |
928494 |
751482.9 |
D |
5.25 |
9.6 |
AY=Adjusted yield, TC/ha=Total variable cost per hectare, GB= Growth benefit, NB/ha= Net benefit per hectare, BCR= benefit cost ratio, MRR= marginal rate of return
CONCLUSION
In varying doses, all plant extracts work well to control cabbage aphids. In all experimental treatments, the impact of botanicals at varying concentrations on the degree of cabbage aphid infestation over a one-week period was encouraging. Within a week of the treatments being applied, the degree of cabbage aphid infection dropped. With the exception of the untreated plots, the effectiveness of botanicals improved and the level of cabbage aphid infestation reduced with repeated spraying.
The greater concentration of Endod leaves compared to the usual check. Dimethoate 40EC was associated with reduced aphid infestation levels, higher efficacy, higher head formation, higher stand counts, higher plant heights, higher canopy spreads, higher marketable yields, and lower cabbage yield loss percentages. When compared to control plots, Endod with 5% and 7.5% constriction can be indicated as the most economical and effective botanical in creating a substantial high rate of reduction for cabbage aphid management. This enables farmers to use locally available botanical treatments instead of chemical insecticides, increasing protection for non-target creatures and improving environmental safety (Mubayrik et al., 2022; Ayari et al., 2023; Chauhan & Angadi, 2024).
ACKNOWLEDGMENTS: None
CONFLICT OF INTEREST: None
FINANCIAL SUPPORT: None
ETHICS STATEMENT: None
Abaynew, J. J., Birara Yalew, M., & Tadesse, T. (2020). Effect of seeding rate and inter-row spacing on yield and yield components of upland rice (Oryza sativa L.) at Libo Kemkem district, Northwestern Ethiopia. International Research Journal of Applied Sciences, 2(1), 12–21.
Abbott, W. S. (1925). A method of computing the effectiveness of an insecticide. Journal of Economic Entomology, 18(2), 265–267.
Abdelmuhsin, A. A., Alghamdi, A. A., & Ibrahim, N. A. (2022). Evaluating the phenotypic and genotypic diversity of plantago ciliata in the Ha’il Region, Saudi Arabia. International Journal of Veterinary Research and Allied Sciences, 2(1), 15–23. doi:10.51847/Qd2C6vFTgc
Aklilu, S., Selamawit, K., Yosef, A., Jibicho, G., Gebyhu, W., Tesfa, B., & Melkamu, E. (2019). Achievement, gaps and future direction on vegetable crops research at Melkassa. MERCI project TERRA project.
AlHussain, B. S., AlFayez, A. A., AlDuhaymi, A. A., AlMulhim, E. A., Assiri, M. Y., & Ansari, S. H. (2022). Impact of different antibacterial substances in dental composite materials: a comprehensive review. International Journal of Dental Research and Allied Sciences, 2(1), 1–7. doi:10.51847/jg2xu2PbJK
Alula, M., & Tesfaye, A. (2021). Survey and management of cabbage aphid (Brevicoryne brassicae L.) on cabbage using botanical extracts under irrigation condition at Dera district, North West, Ethiopia. Stechnolock Plant Biology and Research, 1, 1–23.
Amuji, C. F., Echezona, B. C., & Dialoke, S. A. (2012). Extraction fractions of ginger (Zingiber officinale Roscoe) and residue in the control of field and storage pests. Journal of Agricultural Technology, 8(6), 2023–2031.
Ayari, N., Nasri, S., Moussa, A. B., Hadyaoui, D., Nouira, Z., Harzallah, B., & Cherif, M. (2023). Awareness of deep margin elevation among various dental specialists in Saudi Arabia. Turkish Journal of Public Health Dentistry, 3(1), 1–8. doi:10.51847/0F2hyAtamJ
Begna, F. (2014). Evaluation of botanical insecticides for managing diamondback moth, Plutella xylostella L. (Lepidoptera: Plutellidae) on head cabbage (M.Sc. Thesis). Haramaya University, Haramaya.
Begna, F., & Tebkew, D. (2015). Evaluation of four botanical insecticides against diamondback moth, Plutella xylostella L. (Lepidoptera: Plutellidae) on head cabbage in the central Rift Valley of Ethiopia. Sky Journal of Agricultural Research, 4(5), 97–105.
Bhat, B. R., & Dhoj, Y. D. (2005). Effect of Melia azedarach on aphid (Brevicoryne brassicae) of organic cabbage farming. In 15th IFOAM Organic World Congress (p. 664).
Chane, H. M., & Jenber, A. J. (2025). Efficacy of botanicals against rice weevil (Sitophilus oryzae (L)) on stored sorghum. Indian Journal of Entomology, 87(2), 243–247. doi:10.55446/IJE.2024.2143
Chauhan, A., & Angadi, P. V. (2024). Exploring the awareness and utilization of the metaverse in dentistry among dental students and professionals. International Journal of Dental Research and Allied Sciences, 4(1), 35–43. doi:10.51847/NOf6a25RWu
CIMMYT Economics Program. (1988). From agronomic data to farmer recommendations, an economics training manual (p. 27).
CSA. (2021). Central Statistical Agency. Agricultural sample survey 2018/19 volume 1, report on area and production of major crops private peasant holdings, Meher season (Statistical Bulletin 589). Federal Democratic Republic of Ethiopia, Addis Ababa.
Desale, G., & Getnet, A. (2018). Evaluation of selected botanical aqueous extracts against cabbage aphid (Brevicoryne brassicae L.) (Hemiptera: Aphididae) on cabbage (Brassicae oleraceae L.) under field condition in Kobo District, North Wollo, Ethiopia. Journal of Horticulture and Forestry, 10(5), 69–78.
Emana, B., Afari-Sefa, V., Fekadu, D., Ayana, A., Balemi, T., & Milkessa, T. (2015). Characterization and assessment of vegetable production and marketing systems in the humid tropics of Ethiopia. Quarterly Journal of International Agriculture, 54(2), 163–187.
FAO, & WHO. (2022). Manual on the development and use of FAO and WHO specifications for chemical pesticides (2nd ed., p. 36). Rome & Geneva: FAO and WHO. doi:10.4060/cb8401en
Fiodorova, O. A., Sivkova, E. I., & Nikonov, A. A. (2022). Safeguarding beef cattle from gnats and gadflies in the Southern Tyumen Region. International Journal of Veterinary Research and Allied Sciences, 2(2), 8–13. doi:10.51847/iVXOeXmSNZ
Gebreyohans, G., Yonas, C., Tesfaye, A., & Fasil, A. (2021). Management of cabbage aphid (Brevicoryne brassicae L. (Homoptera: Aphididae) on Ethiopian mustard (Brassica carinata Braun) using entomopathogenic fungi and selected insecticides. SINET: Ethiopian Journal of Science, 44(1), 13–26.
Gonfa, K., & Shiberu, T. (2022). Laboratory evaluation of indigenous botanical aqua extracts against cabbage aphids, Brevicoryne brassicae L. (Hemiptera: Aphididae) on cabbage (Brassicae oleracea). International Journal of Fauna and Biological Studies, 9(1), 45–48.
Griffin, R. P., & Williamson, J. (2012). Cabbage, broccoli and other cole crop insect pests. South Carolina: Clemson University, HGIC, Leucinodes orbonalis.
Habtamu, T., & Mnuyelet, J. (2022). Influences of inter- and intra-row spacing on the growth and head yield of cabbage (Brassica oleracea var. capitata) in western Amhara, Ethiopia. Open Agriculture, 7(1), 392–400.
Hackenberg, B., Schlich, M., Gouveris, H., Seifen, C., Matthias, C., Campus, G., Wolf, T. G., Muthuraman, M., & Deschner, J. (2023). Perceived competence of dental students in managing medical emergencies: a cross-sectional study. Annals Journal of Dental and Medical Assisting, 3(1), 20–25. doi:10.51847/SlNUqaRTG2
Hines, R. L., & Hutchison, W. D. (2013). Cabbage aphids. VegEdge, Vegetable IPM Resource for the Midwest. University of Minnesota, Minneapolis, MN, p. 316–352.
Iqbal, M. F., Kahloon, M. H., Nawaz, M. R., & Javaid, M. I. (2011). Effectiveness of some botanical extracts on wheat aphids. The Journal of Animal and Plant Sciences 21(1):114-115.
Isman, M. B. (2000). Plant essential oils for pest and disease management. Crop Protection, 19(8–10), 603–608.
Jenber, A. J., Birhanu, E., & Teferi, B. (2024). Integrated management of onion thrips (Thrips tabaci L.) and its effect on onion growth and yield (Allium cepa L.) under irrigation conditions in Gubalafto District, Northeastern Ethiopia. International Journal of Agricultural and Natural Sciences, 17(1), 61–79. https://www.ijans.org/index.php/ijans/article/view/826
Kapoor, B., & Sharma, K. (2020). Biorational pesticides: an envirosafe alternative to pest control. Indian Farmer, 7, 722–733.
Kassahun, Y. (2018). Effect of tobacco concentration (Tobaccumrestica) to protect cabbage aphid (Brevicornyebrassicae) on cabbage crop (Brassica oleracea). Indian J. Entomology, 6, 299–304.
Kumar, D., Gurunathan, D., Jabin, Z., & Talal, S. (2022). Comparative efficacy of aromatherapy and conscious sedation in pediatric dental anxiety management. Annals Journal of Dental and Medical Assisting, 2(1), 14–21. doi:10.51847/TVRFhVaiIQ
Kumar, S. N., & Tayde A. R. (2019). Evaluation of selected botanical extracts against cabbage aphids (Brevicoryne brassicae L.). J. Entomology and Zoology Studies, 7(5), 1414–1416.
Lanjar, Z. S., Chang, B. H., & Khuhro, N. A. (2017). Comparative efficacy of leaf extracts of tobacco varieties against cabbage aphid Brevicoryne brassicae Linnaeus (Homoptera: Aphididae). Sci. Int. (Lahore), 29(1), 271–274.
Lidet, S., Gashawbeza, A., & Tadele, T. (2008). Effect of neem-based insecticides on cabbage aphid (Brevicoryne brassicae) and its predator in the central Rift Valley of Ethiopia. Pest Management Journal of Ethiopia, 12, 59–66.
Mahmood, H., Shahid, A. M., Usama, M., Nadeem, E., Zafar, N., & Bashir, R. (2022). Knowledge and perception of periodontal-systemic interactions among dental professionals. Annals of Orthodontics and Periodontics Specialty, 2, 23–28. doi:10.51847/BbcDtqLmI1
Megersa, A. (2016). Botanicals extract for control of pea aphid (Acyrthosiphon pisum; Harris). Journal of Entomology and Zoology Studies, 4(1), 623–627.
Mengistie, B., Arthur, P. J. M., & Peter, O. (2017). Pesticide use practices among smallholder vegetable farmers in Ethiopian Central Rift Valley. Environment, Development and Sustainability, 19, 301–324.
Ministry of Agriculture (MoA). (2019). Crop Register No. 21. Plant Variety Release, Protection and Seed Quality Control Directorate. Addis Ababa, Ethiopia, 231.
Mubayrik, A. F. B., Al-Turck, K., Aldaijy, R. E., Alshehri, R. M., Bedaiwi, A. A., Alofisan, A. O., AlMani, S. A., & Alsuiati, Y. A. (2022). Understanding the dangers of sun exposure and the importance of photoprotection practices in public awareness. Turkish Journal of Public Health Dentistry, 2(1), 1–8. doi:10.51847/32g0nPWudc
Mulu, E., Jenber, A. J., Tesfaye, A., & Belay, B. (2023). Integrated management of onion thrips on onion, Mecha District, Ethiopia. World Journal of Environmental Biosciences, 12(1), 32–40. doi:10.51847/bbmj8P5dll
Negreiros, A. B., Silva, G. R. D., Pereira, F. D. M., Souza, B. D. A., Lopes, M. T. D. R., & Diniz, F. M. (2024). Evidence of genetic diversity gradients in melipona rufiventris (hymenoptera: apidae) within the Brazilian Semiarid Region. Entomology Letters, 4(1), 1–7. doi:10.51847/l9Wmr8r6qW
Opfer, P., & McGranth, D. (2013). Oregon vegetables, cabbage aphid and green peach aphid. Department of Horticulture, Oregon State University, Corvallis, OR, Disponível, 20, 13–21.
Patel, A. K., Joshi, D., Khan, A., Jaisval, G. K., Kumar, A., Pathania, R., & Kushwaha, T. N. (2024). Biology, diversity, distribution, and characterization of Brevicoryne brassicae (L) cabbage. International Journal of Plant & Soil Science, 36(3), 336–347.
Prada, A. M., Cicalău, G. I. P., & Ciavoi, G. (2024). Resin infiltration for white-spot lesion management after orthodontic treatment. Asian Journal of Periodontics and Orthodontics, 4, 19–23. doi:10.51847/ZTuGEanCSV
Pratiksha, M. (2022). Effect of different varieties and spacings on growth and yield attributes of cabbage (Brassica oleracea var. capitata L.) under Lucknow conditions. The Pharma Innovation Journal, 11(3), 1174–1178.
Sarwar, M. (2015). The killer chemicals for control of agriculture insect pests, the botanical insecticides. International Journal of Chemical and Biomolecular Science, 1(3), 123–128.
Shiberu, T., & Mulugeta, N. (2016). Effects of synthetic insecticides and crude botanicals extracts on cabbage aphid, Brevicoryne brassicae (L.) (Hemiptera: Aphididae) on cabbage. J Fertil Pestic, 7(1), 1–5.
Shonga, E., & Getu, E. (2021). Efficacy of plant derived and synthetic insecticides against cabbage aphid, Brevicoryne brassicae (L.) (Homoptera: Aphididae) and their effect on coccinellid predators. SINET: Ethiopian Journal of Science, 44(1), 27–37.
Spirito, F. D., Iacono, V. J., Alfredo, I., Alessandra, A., Sbordone, L., & Lanza, A. (2022). Impact of COVID-19 Awareness on Periodontal Disease Prevention and Management. Asian Journal of Periodontics and Orthodontics, 2, 16–26. doi:10.51847/t8D9TJGOCU
Tekle, B., & Tesfu, N. (2023). Analysis of head cabbage value chain in Guji Zone, Southern Oromia, Ethiopia. International Journal of Agricultural Economics, 8(1), 14–26.
Tesfaye, A., Jenber, A. J., & Mintesnot, M. (2021). Survey of storage insect pests and management of rice weevil, Sitophilus oryzae, using botanicals on sorghum (Sorghum bicolor L.) at Jawi District, Northwestern Ethiopia. Archives of Plant Protection and Phytopathology, 54(19–20), 2085–2100. doi:10.1080/03235408.2021.1970976
Tilahun, N., Hassen, S., & Tefera, R. (2019). Fungicidal management of garlic rust (Puccinia allii) and assessment of yield losses due to the disease. Journal of Plant Pathology and Microbiology, 10, 471.
Yechale, M., Assefa, A., & Jenber, A. J. (2021). Sowing methods and seeding rates effects on yield and yield components of Tef (Eragrostis tef [Zucc.] Trotter) at Adet, North West Ethiopia. Heliyon, 7(3):e06519. doi:10.1016/j.heliyon.2021.e06519
Zahid, S. M. A., Arshad, M., Murtaza, G., Ali, S., Aaqib, M., Yousaf, R. W., & Hussain, S. (2016). Synergistic effect of plant extracts with synthetic insecticides against citrus mealy bug Planococcus citri (Pseudococcodae: Homoptera). Journal of Agricultural Studies, 1, 1–7.
Zakinyan, R. G., Badakhova, G. K., Lopteva, M. S., Koshkina, N. A., Tolokonnikov, V. P., & Povetkin, S. N. (2023). The link between ixodid tick populations and climate change in the Stavropol Region. Entomology Letters, 3(2), 38–43. doi:10.51847/4lXTZ8h0Bs
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