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IOP Conference Series: Earth and Environmental Science

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Impact of biopesticide inundation on the diversity of soybean pests and


diseases
To cite this article: MSYYI Prayogo et al 2021 IOP Conf. Ser.: Earth Environ. Sci. 743 012003

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Impact of biopesticide inundation on the diversity of soybean


pests and diseases

Y Prayogo, MSYI Bayu, GWA Susanto, SW Indiati


Indonesian Legumes and Tuber Crops Research Institute, Jl. Raya Kendalpayak KM
08, Po. Box 66, Malang 650101, East Java, Indonesia

E-mail: [email protected]

Abstract. Soybean pests and diseases are quite abundant and have shown the resistance to
chemical pesticides. Biopesticides are biological agents derived from plant metabolites and
microorganisms. They are effective for controlling pests and diseases as well as suppress the
resistance and resurgence. This research aimed to study the impact of biopesticide inundation
on soybean pests and diseases. The study was conducted in Banyuwangi, East Java.
Biopesticides applied were Trichoderma harzianum (Trichol 8), neem seed powder,
entomopathogenic virus SlNPV (Virgra), entomopathogenic fungi Beauveria bassiana, and
eugenol from clove oil. The results showed that biopesticide applied by inundation can
suppress Sclerotium rolfsii, Phakopsora pachyrhizi, Xanthomonas axonopodis, and Spodoptera
litura. The application of biopesticides by inundation is safer and can maintain the survival of
natural enemies and can reduce yield losses. However, the application of chemical can kill
natural enemies. Oxyopes sp., Coccinella sp., Sycanus sp., Andrallus sp., Rhynocoris sp.,
Paederus sp., Entomobrya sp., Aphidius sp., Binodoxys sp., Encarsia sp., Trichogramma sp.,
and Telenomus sp. which survived on field applied with biopesticides is quite abundant.
Therefore, natural enemies have a great opportunity as biological agents for controlling
soybean pests and diseases and as an alternative to replace the use of chemical.

1. Introduction
National soybean productivity is still relatively low, which is only 0.8-1.2 t/ha, meanwhile the
potential yield from superior varieties can reach 3 t/ha. The key factor interfering the soybean yield is
the presence of pests and diseases. There are numerous main pests of soybean that attack from early
growth up to harvest. In the early growth,soybean was vulnerable to bean fly (Ophiomyia phaseoli),
stem borer (Melanagromyza sojae), and shoot borer (M. dolichostiqma) [1-2]. In vegetative phase,
there are armyworm (Spodoptera litura), leaf-rollers (Lamprosema indicata), caterpillars
(Chrysodeixis chalcites), and whitefly (Bemisia tabaci) [3-4]. Furthermore, during generative phase,
there are pod sucking pests consisting of brown stink bugs (Riptortus linearis), green stink bugs
(Nezara viridula), pale-green stink bugs (Piezodorus hybneri) [5], and pod borer (Etiella zinckenella)
[6-7]. Soybean yield losses due to pests may reach 80% and even puso if there are not controlled [8].
Another biotic factor that plays a significant role in reducing soybean yield is pathogen infection.
Important disease in the early growth of soybean is soil borne disease caused by fungi (Rhizoctonia
solani and Sclerotium rolfsii). The symptoms of plants infected with R. solani and S. rolfsii are wilting
and dying suddenly. The development of the disease in field is very fast, especially in high humidity
condition through the spread of sclerotia and mycelium as infective organs [9-10]. The important

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

diseases in the vegetative to generative phases are leaf rust (Phakopsora pachyrhizi), downy mildew
(Perenospora manshurica), and powdery mildew (Microsphaera diffusa) [11-12]. These three kinds of
disease cause necrotic leaves. The severe attack causes leaves to be dry out and fall down prematurely
[13-14]. Another disease that is no less important is the soybean mosaic virus (SMV), which is
transmitted by B. tabaci or Aphis glycines [15]. Symptoms of SMV are curling leaves and stunted
plants so that cause yield losses up to 80% and crop failure [16].
Generally, pest control technology applied by farmers is the intensive use of chemical pesticides,
but the pest population in the field increased continuously. It occurred due to some kinds of pests build
a resistance to most chemical pesticide formulations. This condition is triggered by increasing the
intensive use of chemical pesticides with excessive dosages so that an insect will survive, build
immunity and produce offspring with high tolerance [17-18]. In addition, the application of chemical
pesticides with inappropriate doses and broad spectrum cause the resurgence or explosion of
secondary pests and destroying all existing natural enemies [19]. The study by [20] indicated that
chemical insecticides containing active ingredients chlorpirifos, indoxacarb and flubendiamide were
more toxic to predators of the Coccinellidae family as compared with spinosad. The increase of the
intensive exploitation of chemical pesticides does not only seem to destroy the target pest, but also all
natural enemies so that pest outbreak will occur.
An effort to prevent pest outbreak can be done with the alternative control, namely biopesticides
[21-22]. Biopesticides are biological pesticides from plants, pathogens such as viruses and
entomopathogenic fungi, and predators. Neem seed powder (Azadirachta indica), eugenol from clove
oil (Syzygium aromaticum), entomopathogenic virus (Spodoptera litura nuclear polyhedrosis virus)
(SlNPV), entomopathogenic fungi (Beauveria bassiana), and antagonistic fungi (Trichoderma
harzianum) that applied by inundation was reported effectively suppress the population and inhibit the
outbreak of major soybean pest and disease [13], [23-24]. In addition, other research also reported that
the application of biopesticides is safer and environmentally friendly so that it can maintain the
survival of beneficial insects, both predators and parasitoids [25-27]. Based on the reason above, this
research aims to study the impact of biopesticides inundation on major soybean pest, pathogen and
natural enemies disease populations.

2. Methods
This research was conducted in Kedungasri Village, Tegaldlimo district, Banyuwangi, East Java, on
March – July 2018. Banyuwangi was chosen as the location of this technology development because
Banyuwangi is a soybean production center in East Java. In addition, the use of chemical pesticides
carried out by farmers in these locations is very intensive, the application is done weekly even though
the pest population was not dangerous. Therefore, most chemical pesticide formulations at the location
were no longer effective for suppressing the pest population, and there were pest outbreaks in each
growing season.

2.1 Experimental set-up


The total area used was 15 hectares of ex-paddy rice fields consisting of 10 ha area for control
technology by using biopesticides. The biopesticides used were; (1) Trichol 8, biofungicide containing
Trichoderma harzianum, (2) NSP, plant-based pesticide from neem seed powder, (3) Virgra,
entomopathogenic virus containing SlNPV, (4) BeBas, entomopathogenic fungus (Beauveria
bassiana), (5) Eugenol, a vegetable pesticide containing clove oil. In addition, an area of ​ ​ 5 ha was
used for control technology using chemical pesticides from Benomyl (fungicide), Captan,
Deltamethrin and Sipermetrin (insecticide) (Table 1). Soybean varieties used were; (1) Anjasmoro
(large seeds), (2) Argomulyo (large seeds), and (3) Martoloyo (Banyuwangi local varieties with small
seeds). Ex-paddy rice fields without tillage (TOT) then made drainage channels in each 4 m plot. The
width of drainage channel was 20 cm and depth of 25 cm. Soybean seeds were treated by using
Trichol 8 in the biopesticide technology plot, while the seeds in the chemical pesticide technology plot
was treated by using benomyl. Both seed treatments were used to suppress the infection of soil borne
pathogen (S. rolfsii & R. solani). Seed was planted by inserting into a hole, the plant spacing used is
40 cm x 15 cm, with two seeds in each hole.

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Table 1. Technology component of soybean cultivation by using biopesticides and chemical pesticides
No. Component Soybean cultivation technology
Chemical insecticide (5 ha) Biopesticide (10 ha)
1. Land Preparation Herbicide before planting (non Straw was burned before planting
tillage/ minimum tillage) (non tillage)
2. Drainage At each 4 m (width: 20 cm, deepth: At each 4 m (width: 20 cm, deepth:
25 cm) 25 cm)
3. Seed High quality, vigor >80% High quality, vigor >80%
4. Seed treatment captan & sipermethrin Trichol 8
5. Variety Argomulyo, Anjasmoro, Martoloyo Argomulyo, Anjasmoro, Martoloyo
(local) (local)
6. Plant method Tugal Tugal
7. Plant spacing 40 cm x 15 cm 40 cm x 15 cm
8. Organic fertilizer 2 t/ha 2 t/ha
9. Anorganic 200 kg Phonska + 100 kg SP 36/ha 200 kg Phonska + 100 kg SP 36/ha
fertilizer
10. Liquid fertilizer 5 ml/l (20, 40, 60 DAP) 5 ml/l (20, 40, 60 DAP)
11. Weeding Herbicide (15-20 DAP) Manual (15-20 DAP)
12. Pest and disease Chemical pesticide (scheduled) Biopesticide (Inundation)
control Benomyl, sipermethrin, Virgra, BeBas, Trichol 8, NSP,
deltamethrin Eugenol
13. Harvesting time Brown pods Brown pods

Note: NSP (neem seed powder), Trichol 8 (T. harzianum), Virgra (SlNPV), BeBas (B. bassiana),
eugenol (clove oil).

Weeds were sprayed using herbicides at 15-20 (DAP) and at 28-30 HST weeding was done
manually. In addition, in biopesticide technology plot, straw were burned before planting and at 28-30
DAP, weeding was done manually. Pests and diseases controlled by using chemical pesticides made
from Benomyl (fungicide), Deltamethrin, and Sipermetrin (insecticide) applied scheduled. However,
biopesticide technology used were five kinds namely Trichol 8, NSP, Eugenol, Virgra, and BeBas
(Table 2).
The observed variables are: (1) Kind of pest and population, observed visually in 10 plants and
catching insects by sweep net in a single swing for five times, as many as five points diagonally per
plot; (2) Kinds and diseases intensity, observed based on diseases incidence for soil borne diseases and
diseases severity for air borne diseases; (3) plant growth, (4) yield components (number of filled and
hollow pods), (5) seed weight per hectare (t/ha); and (6) abundance of insects as natural enemies
(predators and parasitoids).

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Table 2. Kind of pests, economic threshold, kinds and application time of chemical pesticides and
biopesticides
No. Kind of pests and Economic Application time (DAP)
diseases threshold Chemical pesticide Biopesticide
Pest

1. S. litura, C. chalcites, 10 individuals instar Cyhalotrin (21, 28, 35, SBM + Virga (28,
L. indicata III/10 plant at 42, 49) 35, 42)
flowering phase atau
13 individuals/10
plants as pod filling

2. B. tabaci 1 pair of adult/100 Amitraz (28, 35, 42, BeBas (35, 42, 49)
plants at 28 DAP 49, 56)

3. R. linearis, N. 1 pair of adult/20 Sipermethrin (42, 49, BeBas (42, 49, 56)
viridula, P. hybneri plants at 35 DAP 56, 63, 70)

4. E. zinckenella, H. 2 individuals/plant Sipermethrin (42, 49, Virgra+BeBas (42,


Armigera at 42 DAP 56, 63, 70) 49, 56)

Disease

1. R. solani, S. rolfsii DS=10% Captan (seed Trichol 8 (seed


treatment) treatment)
Mankozeb (7, 14, 21, Trichol (14, 21,
28, 35) 28)
2. P. pachyrhizi DS=35% Benomyl (35, 42, 49, Eugenol (35, 42,
56, 63, 70) 49)

2.2 Data analysis


Data were subjected to analysis of variance (ANOVA) and mean values were compared using Tukey’s
test when significant F values were obtained (α = 0.05; SPSS ver. 22).

3. Results and discussion

3.1 Pests population


Based on visual observations and catching the insect by using sweep net, several kinds of orders were
obtained including Homoptera, Hemiptera, Orthoptera, Diptera and Lepidoptera (Table 3). The highest
population was B. tabaci, both in soybean plants that are applied with biopesticides and chemical
pesticides. The population of B. tabaci at 49 DAP in the biopesticides plot was lower (43.10
individuals), while in the chemicals plot it reached 80.40 individuals. However, at 63 DAP, the
population of B. tabaci in the biopesticide plot was higher (154 individuals), while the population of B.
tabaci on the chemical pesticides plot was 96 individuals.
Another pest from the order of Homoptera obtained was Empoasca sp. with the highest population
in the biopesticide plot 2.60 individuals at 49 DAP and 11 individuals at 63 DAP. However, in the
chemical pesticide plot only 2.30 were found at 49 and 63 DAP. The Hemiptera insect caught were R.
linearis with a low population (0.10-1.50 individual). M. sojae and M. dolichostigma were also
successfully caught using sweep net in large population, especially M. dolichostigma (17 individuals)
in biopesticide plot at 63 HST. The population of M. dolichostigma in the chemical pesticide plot was
also quite high (10.60 individuals). However, the population of M. sojae caught was 4.80 individuals

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

on chemical pesticide plot at 63 DAP. The pests from the order of Lepidoptera caught were S. litura, L.
indicata, and E. zinckenella. The population of these three types of insects is quite low based on visual
observation on 10 clumps of plants.

Table 3. The population of arthropods in soybean fields applied with biopesticides and chemical
pesticides
Population average at the DAP (individual)
No. Kind of arthropods Biopesticide Chemical pesticide
49 63 49 63

1. Empoasca sp. (Homoptera: Cicadelidae) 2.6 11.0 2.3 2.3


2. B. tabaci (Homoptera: Aleyrodidae) 43.1 154.0 80.4 96.0
3. R. linearis (Hemiptera: Alydidae) 0.1 1.5 0.2 0.5
4. Valanga sp. (Orthoptera: Acrididae) 1.4 1.0 0.6 4.0
5. M. sojae (Diptera: Agromyzidae) 0.1 0.0 1.5 4.8
6. M. dolichostigma (Diptera: Agromyzidae) 0.3 17.6 1.4 10.6
7. S. litura (Lepidoptera: Noctuidae) 2.3 0.0 2.1 0.0
8. L. indicata (Lepidoptera: Noctuidae) 0.9 1.5 0.0 0.5
9. E. zinckenella (Lepidoptera: Pyralidae) 0.0 0.9 0.0 0.5

3.2 Pest attack intensity


The observations on three varieties showed that the symptoms of armyworm attack appeared with very
low intensity (1.5-5%), both in the biopesticides plot and chemical pesticides plot (Figure 2). The
performance of the plants was quite good, there was no significant damage (Figure 3). The intensity of
S. litura attack was very low, still below the economic threshold, which is 10 larvae of third instar / 10
clumps at floweing time and 13 larvae / 10 clumps during pod filling.
The highest intensity of B. tabaci attack was found in the plot that applied with biopesticides,
namely Anjasmoro (9.50%), Argomulyo (9%), and Martoloyo (6.50%). However, the intensity of B.
tabaci attacks on plot that applied using chemical pesticides was lower about 3-5% (Figure 4).

Figure 2. The intensity of S. litura attack on three soybean varieties on plot applied by
biopesticides and chemical pesticides.

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Figure 3. Performance of soybean plants applied with biopesticides (left) and chemical pesticides
(right).

Figure 4. The intensity of B. tabaci attack on three soybean varieties on plot applied by
biopesticides and chemical pesticides

3.3 Kinds and disease intensity


Observation of soil borne diseases were carried out on plants at 21 DAP. The identified soil borne
diseases are caused by Sclerotium rolfsii which can be found on plot applied with biopesticides and
chemical pesticides with intensities about 1.80 to 6.70% (Figure 4). The highest intensity occurred in
the Martoloyo variety in plot applied with captan (6.70%), while the lowest intensity occurred in plot
applied with Trichol 8. There was wilting symptom about 6.70% on seed treatment by using captan, it
was higher than the treatment by using biofungicides.

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Figure 5. The intensity of soil borne diseases (S. rolfsii) and bacterial pustules (X. axonopodis) in the
biopesticide and chemical pesticides plot.

Bacterial pustules caused by X. axonopodis was also found in plot that applied with biopesticides
and chemical pesticides. The average of disease severity that occurs in plot applied with chemical
pesticides was high (9.15%) which found on Martoloyo. However, the average of disease severity of X.
axonopodis on Anjasmoro and Argomulyo in the plot applied with biopesticides was only 2.5%.
Symptoms of bacterial pustules are small, yellowish green spots with a slightly protruding in the
middle, larger patches developing in the middle, light brown bumps on the lower surface. This
protrusions caused by hypertrophy and hyperplasis (Figure 5). The intensity of X. axonopodis disease
in both varieties (Anjasmoro & Argomulyo) was much lower than that of Martoloyo.

Figure 6. Symptoms of bacterial pustules (X. axonopodis) in Martoloyo variety applied using Trichol
8 (left) and chemical fungicides (right).

3.4 The intensity of rush disease (P.pachyrhizi)


The intensity of rust disease was very low, the intensity of this disease in the plots applied with
biopesticides was only 2.20% while, in the plots applied with chemical fungicides was about 6.70%.
However, the intensity of rust disease on farmer’s field around the research site that were not
controlled reached 27.50% (Figure 7).

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Figure 7. The average intensity of rust disease (P. pachyrhizi) in plots applied with biofungicides,
chemical fungicides, and without control (farmer's field).

3.5 Seed Weight


The highest seed weight was obtained on Anjasmoro which were applied using biopesticide (2.98 t /
ha), while the seed weight in the chemical pesticide plots was 2.89 t / ha (Figure 8). Martoloyo variety
can produce seed weight up to 2.81 t / ha on plots applied using chemical pesticides, while in
biopesticide plots, seed weight was low (2.65 t / ha). Seed weight obtained from the Argomulyo
appears to be lower than Anjasmoro and Martoloyo, which wass 2.45 t / ha in chemical pesticides
plots and 2.37 t / ha in biopesticides plots.
Anjasmoro produced higher seed weight as compared to the other two varieties, Argomulyo and
Martoloyo (Table 4). This condition related with the number of node in Anjasmoro was also greater
(21.10) than Argomulyo (16,16) and Martoloyo (18.50). The seed weight of Argomulyo was lower
than Anjasmoro and Martoloyo, but Argomulyo contains half of total number of filled pods from
Martoloyo and Anjasmoro. This incident can be proven from the number of pods on Martoloyo (84
pods), but the number of pods on Argomulyo was only 43 pods. The size of seeds on Argomulyo (16 g)
was much larger than Anjasmoro (14.8-15.3 g) and Martoloyo (10.7 g) [28].

Figure 8. Seeds weight of Anjasmoro, Argomulyo, and Martoloyo from plot applied with
biopesticide and chemical pesticide

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Table 4. Plant height, number of node, filled pods, and empty pods of three soybean varieties on plot
applied with biopesticides and chemical pesticides
Varieties Plant height Number of node Filled pod Empty pod
Biopesticide Chemical Biopesticide Chemical Biopesticide Chemical Biopesticide Chemical

Anjasmoro 66.40 71.81 21.10 22.54 81.40 83.90 0.70 1.40


Argomulyo 69.53 67.35 16.16 17.54 43.61 31.54 1.14 1.18
Martoloyo 83.16 71.76 18.00 16.43 84.84 85.53 1.57 2.23

3.6 Abundance of natural enemies


Many natural enemies was still found on the plot applied with biopesticides, both predators and
parasitoids. There were Oxyopes sp., Coccinella sp., Andrallus sp., Rhynocoris sp., Sycanus sp.,
Paederus sp., and Entomobrya sp. (Figure 9). Predators Coccinella sp., Sycanus sp., Andrallus sp., and
Rhynocoris sp. inhabit plant canopy and they have high ability to predict insect pests that attack the
soybean canopy. However, Oxyopes sp. and Paederus sp. are predators that inhabit soil surface and
also plant canopy, while predators Entomobrya sp. only inhabit soil surface. The population of
predator on plots applied with biopesticides, especially Entomobrya sp., Oxyopes sp., and Paederus sp.
were quite high at 49 to 63 DAP. However, in plots applied with chemical pesticides, no predators was
found to be survived, except Paederus sp. and Entomobrya sp. with very low populations.

Figure 9. Kind and predators population on three soybean varieties on plot applied with
biopesticides and chemical pesticides

The kind of parasitoids that can be found in plot applied with biopesticides were Aphidius sp.,
(Hymenoptera: Braconidae), Binodoxys sp. (Hymenoptera: Braconidae), Trichogramma sp.
(Hymenoptera: Trichogrammatidae), Encarsia sp. (Hymenoptera: Aphelenidae), and Telenomus
sp. (Hymenoptera: Scelionidae). The population of this four kind of parasitoids was quite high at
49 DAP, which is 8, 10, 5, and 21 individuals, respectively. The population of this four
parasitoids at 62 DAP increased significantly, especially Telenomus sp. (82 individuals),
Trichogramma sp. (42 individuals), Aphidius sp. (21 individuals), and Encarsia sp. (11
individuals) (Figure 10).

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

Figure 10. Kind and parasitoids population on three soybean varieties on plot applied with
biopesticides and chemical pesticides.

3.7 Discussion
B. tabaci population at 63 DAP was higher in plots applied with biopesticides as compared to the plots
applied with chemical pesticides. This condition occurs due to the migration of B. tabaci from plots
applied with chemical pesticide to plots applied with biopesticides because of wind. According to [29],
wind speed is one of the environmental factors that cause B. tabaci migration to other places, besides
plant age and plant height. [30] mentioned that wind speed has a positive correlation with B. tabaci
migration.
In both plots were also found M. soyae and M. dolichostigma with high numbers of population. It is
suspected that the abundance of these pests impact on the eggs laid by adult on the plant but the age of
the plant is not appropriate so they only fly over the plant surface. The low population of foliage pest
and pod borer found in plots that applied with biopesticides was due to the use of Virgra. Virgra
contains the active ingredient of the entomopathogenic virus SlNPV so that the larval stage of the
armyworm can be killed due to the virus infection. [31] reported that Virgra is an entomopathogenic
virus formulated from JTM97C isolates and it is very effective for controlling S. litura larval with a
mortality rate of up to 99%. [32] also explained that the control of S. litura was very effective by using
bioinsecticides from SlNPV.
The low intensity of S. litura attacks on plots applied with chemical pesticides because the
scheduled application, farmers also apply chemical insecticides outside the established schedule. This
activity is carried out by farmers based on the reason that cultivated of soybean does not occur damage
even though it must take out excessive input to buy chemical pesticides. SlNPV biopesticide system
requires a minimum of 3-4 days after feed insects (leaves) have been sprayed with a suspension of
virus particles. Thus, larvae still eat soybean leaves, causing damage even though the intensity of the
damaged was only about 5%. In addition, biopesticide plots was also applied with NSP containing
azadirachtin compounds. These compounds originated from vegetable pesticides that plays function to
inhibit the appetite of insects, refuse insects to come to the plants, and thwart the process of moulting.
The low intensity of soil borne diseases in plots applied with Trichol 8 through seed treatment due
to the biofungicide functions as an antagonist, causing root and stem rot. In addition, T. harzianum
plays role as a decomposer so that the litter above the soil surface can immediately be overhauled into
organic fertilizer and can increase plant growth [33-34]. Withering was a major obstacle at the early
growth in soybean production center in Banyuwangi. Seed treatment by using Trichol 8 is able to
suppress wilting in endemic areas, so that control technology innovations by using biofungicides can
be recommended to control S. rolfsii.
The intensity of X. axonopodis disease in both varieties (Anjasmoro & Argomulyo) was much
lower than that in Martoloyo. This condition is likely due to the impact of the application of T.
harzianum biofungicide that given before planting and the application was done at 21, 28, 35 DAP.
This activity caused pathogens to be not able to develop due to better plant vigor [35-36].

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The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

The low intensity of rust disease caused by the application of biofungicides (eugenol). It was
carried out four times at 28, 35, 42 and 49 DAP so can kill P. pachyrhizi spores, as a result, the disease
was unable to develop. [37] reported that eugenol from clove oil is able to damage the uredospora cell
wall so that the spores undergo lysis eventually dry and die. Further, the spores cannot develop. In
addition, the application of NSP can also negatively influence the development of leaf rust as reported
by [38] and [39], who mentioned that the application of azadirachtin compounds from neem seed
powder can reduce the severity of P. pachyrhizi rust disease up to 83%.
In case of seed weight, it appears that soybean pest control technology by using chemical pesticides
can produce higher seed weight as compared with biopesticides. This phenomenon occurs because the
application of chemical pesticides is scheduled, and it is able to kill all pests in a very fast time without
pay attention to the pest population. Therefore, there is no chance for these organisms to damage
plants, especially pods. Meanwhile, the efficacy of biopesticides which are applied in a slower
inundation which takes a minimum of 3-4 days so that the insect still doing activities to damage the
plant.
In plots applied with chemical pesticides, there were no predators found and survived, except
Paederus sp. and Entomobrya sp. even though the population is very low. This condition occured due
to the habitat of these two predators are in soil surface. Paederus sp. has fairly high mobility so that
the application of chemical pesticides does not have a negative impact on the behavior of these
predators. Predator Rhynocoris sp. has a high predation rate of S. litura up to 20 individuals/day [40].
While, predators Sycanus sp. if they prey on S. litura larvae, they have a life span up to 88 days [41].
Predator Oxyopes sp. has the ability to prey on several kinds of major soybean pests such as B. tabaci,
A. gossypii, Empoasca sp., and Nezara viridula [42]. The ability of P. fuscipes is also very high for
preying on Helicoverpa armigera [43]. Meanwhile, these two predators (Oxyopes sp. and Paederus
sp.) have the ability to prey the major soybeans pest up to 11 individuals/day [44-45]. Predator
Entomobrya sp. is a predator that inhabit soil surface. Entomobrya sp. also play role as a decomposer
insect that is effective in overhauling all soil litter. It is very useful to provide nutrients for the plant
quickly [30], [46]. The abundance of various species of predator that survived on plots applied with
biopesticides have considerable potential as biological agents to prey soybean pests.
Each parasitoid has a high level of parasitation against major soybean pests such as B. tabaci, A.
craccivora, A. gossypii, and S. litura [47-50]. The increasing in parasitoid populations in plots applied
with biopesticides was not followed in plots applied with chemical pesticides because most of the
parasitoids were killed. This phenomenon occurs because natural enemies, especially parasitoids, are
more susceptible to chemical insecticides than the pest, while parasitoids act as natural controllers.
According to [51], insecticides containing active ingredients tiametoksam, lamda sihalotrin,
chlorpyrifos, or chlorphenapy can kill all parasitoids in soybean fields. [52] and [53] stated that the
parasitoid Trichogramma pretiosum and Telenomus remus will be killed by the application of
chemical insecticides. These result indicate that the use of biopesticides derived from microorganisms
and plant-based pesticides is more environmentally friendly, because it can maintain the survival of
natural enemies while being able to suppress the existing pest populations.

4. Conclusions
From this study, we concluded that biopesticides consisting of T. harzianum, SlNPV, NSP, B.
bassiana, and eugenol applied by inundation can suppress the development of pest and disease
populations almost comparable to the efficacy of chemical pesticides. Soybean pest control by using
various kinds of biopesticides by inundation is safer and can maintain the survival of useful insects,
especially predators and parasitoids. It can maintain soybean yield almost comparable to the efficacy
of chemical pesticides. Scheduled application of chemical pesticides can kill almost all existing natural
enemies, both predators and parasitoids. Biopesticides applied by inundation can potentially be used as
alternatives to the efficacy of chemical pesticides.

11
The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

References
[1] Arnemann J A, Tay W T, Walsh T K, Brier H, Gordon K, Hickmenn F, Ugalde G and Guedes J V
C 2016 Soybean stem fly, Melanagromyza sojae (Diptera: Agromyzidae) in the new world:
Detection of high genetic diversity from soybean field in Brazil Genetic and Molecular
Research 15 1-13.
[2] Abdel_Raheem M A and Al-Keridis L A 2017 Virulence of three entomopathogenic fungi against
whitefly Bemisia tabaci (Gennadius) (Homoptera: Alydidaea) in tomato crop. Journal of
Entomology 14 155-159.
[3] Mansour S A A, Raff M N M, Khalid A S, Ismail A and Idris A G 2013 Population abundance of
whitefly Bemisia tabaci (Genn.) on chilli an other vegetable crops under glass house
conditions. Journal Tropical Agriculture and Food Scince 41 149-157.
[4] Biswas G C 2013 Insect pest of soybean (Glycine max L.) their nature of damage and succession
with the crop stages. Journal Asia Society Bangladesh Science 39 1-8.
[5] Kusuma M 2014 Kajian aspek ketahanan beberapa genotipe kedelai terhadap hama pengisap
polong Riptortus linearis F (Hemiptera: Alydidae) [Thesis] Universitas Gadjah Mada
Yogyakarta.
[6] Melo M and Silveira E P 1998 Pod borer Etiella zinckenella (Treit.) (lepidoptera: Pyralidae)
damage to common bean Anais da Sociedade Entomologica do Brasil 27 477-479
[7] Apriyanto D, Ogie H Y and Mulyadi A 2009 Performance of soybean pod borer, Etiella
zinckenella treitschke (Lepidoptera: Pyralidae), and host preference on soybean and
groundnut Akta Agrosia 12 62-67
[8] Arifin M and Tengkano W 2011 Tingkat kerusakan ekonomi hama kepik cokelat pada kedelai.
Jurnal Penelitian Pertanian Tanaman Pangan 27 47-54.
[9] Pinheiro Vd R, Seixas C D S, Godoy C V, Soares R M, MCNde O and Almeida A M R 2010
Development of Sclerotium rolfsii sclerotia on soybean, corn, and wheat straw, under
different soil temperatures and moisture contents. Pesq Agropec Brasillia 45 332-334.
[10] Kator L, Hasea Z H and Oche O D 2015 Sclerotium rolfsii: causative organism of Southern
blight, stem rot, white mold and sclerotia rot diseases. Annual of Biology Research 6 78-89.
[11] Hardaningsih S 2011 Jenis penyakit kedelai dan efektivitas jamur antagonis yang berasal dari
Kalimantan Selatan terhadap Sclerotium rolfsii di laboratorium. (SUPERMAN) Suara
Perlindungan Tanaman 1 23-25.
[12] Hardaningsih S 2012 Penyakit kacang-kacangan pada lahan kering masam di propinsi Lampung.
(SUPERMAN) Suara Perlindungan Tanaman 2 22-26.
[13] Murithi H M, Beed F, Tukamuhabwa P, Thomma B P H J and Joosten M H A J 2016 Soybean
production in eastern and southern Africa and threat of yield loss du to soybean rust caused
by Phakopsora pachyrhizi. Plant Pathology 5 176-188.
[14] Tuong H M, Truong T T, Lien T T P, Ha C H and Son L V 2016 Analysis of powdery mildew
resistant characterizatic and genetic relationship of cultivated soybean, Glycine max in
Vietnam for parental selection. International Journal of Bioscience Biochemical and
Bioinformation 6 105-113.
[15] Burrows M E L, Boerboom M C and Gaska J M 2015 The relationship between Aphis glycines
and soybean mosaic virus incidence in different pest management systems. Plant Disease 89
926-924.
[16] Mandhare V K and Gawade S B 2010 Effect of seed borne soybean mosaic virus infection on
quality and yield parameters in soybean. Agricultural Research Communication Centre.
Legume Research 33 43-43.
[17] Kontsedalov S, Abu-Moch F, Labedev G, Czosnek H, Horowitz A R and Ghanim M 2012
Bemisia tabaci biotype dynamics and resistance to insecticides in Israel during the years
2008-2010. Journal of Integrative Agriculture 11 312-320.
[18] Tabasian H, Ravan S, Bandani A R and Siahsar B A 2014 The effect of esterase activity in
resistance of Aphis gossypii to selective insecticides. Science and Technology 8 1128-1112.
[19] Ndakidemi B, Mtei K and Ndakidemi P 2016 Impacts of synthetic and botanical pesticides on
beneficial insects Agricultural Sciences 07 364-372

12
The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

[20] Natikar P K, Vinod M, Mallapur and Balikai R A 2016 Effect of newer insecticides on
populastion of natural enemies and yield of soybean. Journal Exp. Zoology India 19 492-497.
[21] Oguh C E, Ogechi O C, Ubani C S and Okekeaji U 2019 Natural pepticides (Biopesticides) and
uses in pest management- a critical review Environmental Toxicology 2 1-18
[22] Mnif I, Ghribi D 2015 Potential of bacterial derived biopesticides in pest management. Crop
Protection 77 52-64.
[23] Indiati S W 2014 The use of sugar apple and neem extract to control leaf-eating pest on soybean.
Journal of Exp Biology and Agriculture Science (JEBAS) 2 208-214
[24] Sumartini 2015 CEKA, Fungisida nabati untuk pengendalian penyakit karat pada daun kedelai.
Info Teknologi, Balai Penelitian Tanaman Aneka Kacang dan Umbi.
[25] Landis D, Wratten S D and Gurr G 2000 Habitat management to conserve natural enemies of
arthropod pests in agriculture Annual Review of Entomology 45 175-201
[26] Arena S, Palacios S M, Fenogllo M S and Defago M T 2015 Effects of Melia azedarach extract
on natural enemies of Aphids. Biopesticides International 11 1-11.
[27] Ndakidemi B, Mtel K and Ndakidemi K A 2016 Impacts of synthetic and botanical pesticides on
beneficial insects. Agricultural Science 7 364-372.
[28] [BALITKABI] Balai Penelitian Tanaman Aneka Kacang dan Umbi 2012 Deskripsi varietas
unggul kacang-kacangan dan umbi-umbian. Badan Penelitian dan Pengembangan
Pertanian, Kementerian Pertanian.
[29] Khalid S A N, Noor M R M, Touhidor M R and Ghani I A 2006 Effect of plant height, maturity
and climatic factors on the population of whitefly (Bemisia tabaci) on chilli J. Trop. Agric.
And Fc. Sc. 34 195-206
[30] Zeshan M A, Khan M A, Ali S and Arshad M 2015 Correlation of conductive environmental
conditions for the development of whitefly Bemisia tabaci population in different tomato
genotypes. Pakistan Journal Zoology 47 1511-1515.
[31] Bedjo 2004 Pemanfaatan Spodoptera litura Nuclear Polyhedrosis Virus (SlNPV) untuk
pengendalian ulat grayak (Spodoptera litura Fabricius) pada tanaman kedelai. Buletin
Palawija 7-8 1-9.
[32] Samsudin S 2017 Prospek pengembangan bioinsektisida Nucleopolyhedrovirus (NPV) untuk
pengendalian/prospect of development of Nucleopolyhedrovirus (NPV) bioinsecticide
against Perspektif 15 18
[33] Sharma B L, Sharma M L and Singh S P 2017 Bio-degradation of crop residues by Trichoderma
species vis-a vis nutrient quality of the preparat compost. Sugar Technology 14 174-180.
[34] Kushwaha S K, Kumar S and Chaudhary B 2018 Efficacy of Trichoderma against Sclerotium
rolfsii causing collar rot disease of lentil under in vitro conditions. J of Appl & Nat Sci 10
307-312.
[35] Srivastava M, Vipul K, Mohammad S and Pandey S 2016 Trichoderma-a potential and effective
bio fungicide and alternative source against notable phytopathogens: A revie African Journal
of Agriculture Research 11 310-316
[36] Amaria W , Harni R and Wardiana E 2018 Pengaruh dosis and frekuensi aplikasi biofungisida
trichoderma terhadap infeksi Rigidoporus microporus pada benih karet Jurnal Tanaman
Industri dan Penyebar 5 49
[37] Sumartini 2010 Penyakit karat pada kedelai dan cara pengendaliannya yang ramah lingkungan.
Jurnal Penelitian dan Pengembangan Pertanian 29 107-112.
[38] Jahagirdar S, Patil P V, Patil R H, Bohra B and Vyas B N 2010 Integrated management of Asian
soybean rust caused by Phakopsora pachyrhizi India. International Journal of Plant
Protection 3 289-292.
[39] Shabana Y M, Abdalla M E, Shahin A A, El-Sawy M M, Draz I S and Youssif A W 2017
Efficacy of plant extracts in controlling wheat rust disease caused by Puccinia tricinia.
Egyptian Journal of Basic and Applied Science 4 67-73.
[40] Ullah M I, Altaf N, Afzal M, Ashad M, Mehmood N, Riaz M, Majeed S, Ali S and Abdullah A
2020 Effect of entomopathogenic fungi on the biology of Spodoptera litura (Lepidoptera:

13
The 11th International Conference on Global Resource Conservation IOP Publishing
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012003 doi:10.1088/1755-1315/743/1/012003

noctuidae) and its reduviid predator, Rhynocoris marginatus (Heteroptera: Reduviidae)


International J. og Insect Science 11 11-19.
[41] Sahid A 2019 Aspek biologi Sycanus annulicornis Dohrn. (Herniptera: Reduviidae) yang
dipelihara dengan pakan alternative larva Alphitobius diaperinus Panzer (Coleoptera:
Tenebrionidae) Jurnal Agroekoteknologi Tropikal Lembab 2 50-54.
[42] Ghavani S 2008 The potential of predatory spiders as biological control agents of cotton pests in
Tehran Provices of Iran. Asian Journal Experimental Science 22 303-306.
[43] Winasa I W, Hindayana D and Santoso S 2007 Pelepasan dan pemangsaan kumbang jelajah
Paederus fuscipes (Coleoptera: Staphylinidae) terhadap telur dan larva Helicoverma
armigera (Lepidoptera: Noctuidae) pada tanaman kedelai. Jurnal Ilmu Pertanian Indonesia
3 147-153.
[44[ Udiarto B K, Hidayat P, Rauf A, Pujianto and Hidayat S H 2012 Kajian potensi predator
Coccinellidae untuk pengendalian Bemisia tabaci (Gennadius) pada cabai merah. Journal
Horticulture 22 76-84.
[45] Riaz M and Naqvi S A H 2014 Predation potential of foliage spider and estimates of utilization
curve, niche breadth and overlap in cotton filed from Punjab, Pakistan. Journal of
Biodiversity & Environmental Science 5 364-375.
[46] Ernesto M V, Liberal C N, Ferreira A S, Alves A C F, Zeppelini D, Martins C F, Pereira-
Colavite A and Creau-Duare A J 2018 Hexapoda decomposecrs of serra de Santa Catarina,
Baraiba, Brazil: an area with high potential forconservation of caatinga biodiversity. Biota
Neotropica 18 1-13.
[47] Malik A A Y and Karut K 2012 Parasitism status Bemisia tabaci (Gennadius 1889) (Homoptera:
Aleyrodidae) on different host plants in the Cukurova region of Turkey. Turky Entomology
Den 36 59-67.
[48] Hu J S, Gelman D B and Blackbum M B 2015 Age-specifict interaction between the parasitoid
Encarsia formosa and its host the silverleaf whitefly Bemisia tabaci (Strain B). Journal
Insect Science 2 1-10.
[49] Khan I A and Wan F H 2015 Prey consumption of Encarsia formosa Gahan (Hymenopetra:
Aphelinidae) un-parasitized and parasitized Bemisia tabaci (Gennadius) (Homoptera:
Aleyrodidae) biotype B prey by Coccinella septempunctata L. (Coleoptera: Coccinellidae)
predator. Journal of Entomology and Zoology Studies 3 223-228.
[50] Oliveira R de, Oliveira G M, de Sauza M D S, Burba M A, Vendruscolo J, Nunes E da S,
Nascimento I N and Batista Jd L 2016 Development and parasitism of Encarsia hispida
(Hymenoptera: Aphelenidae) on Bemisia tabaci biotype B in cotton. Academic Journals 11
2266-2270.
[51] Fernandes F L, Bacci L and Fernandes M S 2020 Impact and selectivity of insecticide to
predators and parasitoids Entomobrasilis 3 1-10
[52] Car EL, Bueno AdeF and Bueno R C O 2010 Pesticide selectivity for the egg parasitoid
Telenomus remus. BioControl 55 455-464.
[53] Bueno R C O deF, Parra J R P and Bueno A deF 2012 Trichogramma pretiosum parasitism and
dispersal capacity: a basis for developing biological control programs for soybean
caterpillars. Bulletin of Entomological Research 102 1-8.

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