Plant Bugs (Heteroptera: Miridae) Development and Damage to
Cotton Crop in Uzbekistan
MUSAYEV DILSHOD1, NAVRUZ SATTOROV2, JAMILA ABDULLAEVA3,
MUSAEVA MAKHLIYO2, SAPAROV ABDIRAHMAN4, BAKHTIYOR KHOLMATOV1,
YUSUPOVA ASIYA5, MEDETOV MAXSETBAY1
1Entomology Laboratory, Institute of Zoology,
Bogishamol, str. 232 B 100125, Tashkent, UZBEKISTAN
2Agrotaxology and Food Safety, Institute of Plant quarantine and Protection,
Bobur, str. 4. 111215, Tashkent, UZBEKISTAN
3Department of Ecology, National University of Uzbekistan,
University, str. 4. 100174, Tashkent,
UZBEKISTAN
4Department of Zoology, Human Morphophysiology, Nukus State Pedagogical Institute,
P. Seyitov, str. 2. 230105, Nukus,
UZBEKISTAN
5Department of General Biology and Physiology, Karakalpak State University,
Abdirov str.,1, 230101 Nukus,
UZBEKISTAN
Abstract: - This article provides information on the types of plant bugs, their damage, and measures to
combat them in cotton agrobiocenoses of Uzbekistan. As a result of the conducted research, 15 species of
bugs, of which Eurystylus bellevoyei (Reuter, 1879) species were identified for the first time in the cotton
fields of Uzbekistan. In special experiments in the cages, it was determined that when 100-150 bugs
correspond to 100 cotton plants during the vegetation stage of the cotton plant, cotton yield decreases to
32.3-36.4% owing to the effect of alfalfa bug (Adelphocoris lineolatus) and 8.6-13.5% owing to the plant
bug (Lygus. protensis). If cotton is infected with a cotton shredder bug (Creontiades pallidus) in the early
period (June), the yield of cotton decreases from 61.6% to 88.9%, if there are 30 to 150 plant bugs per 100
cotton plants. If it is infected later (July-August), the yield of cotton decreases from 38.0 to 50.2%. If fine
fiber cotton is damaged by bugs (100-150 specimens per 100 cotton plants) during the vegetation stage, the
cotton yield will decrease by 55.5-65.3% compared to the control variant. The most effective drugs against
plant bugs are: Safegor, 40% (98.3%), Ribo Super, 25% (93.4%), Transform, 50% (92.5%), and Mosetam 20
(82.8-81.9%). Arvilmek 1.8 (active substance- abamectin), Lead, 5% (substance-pymetrozine), Imido Star,
20% (imidacloprid) were found to have unsatisfactory (below 70.0%) results against cotton bugs.
Key-Words: - miridae, cotton bugs, cotton crop, dynamics, agrobiocenosis, population, economic loss,
entomological cage.
Received: October 15, 2022. Revised: February 19, 2023. Accepted: March 17, 2023. Published: April 20, 2023.
1 Introduction
Otherwise, insect pests were estimated to cause an
average annual loss of 7.7% in crop production in
Brazil alone, corresponding to a total annual
economic loss of approximately US$17.7 billion,
[1].
The Heteroptera, commonly called true bugs,
are one of four suborders in the order Hemiptera.
They are one of the most diverse groups of
hemimetabolous insects, comprising more than
45000 species in 91 families worldwide
(http://heteroptera.org/). Globally, the study and
assessment of hemiptera, as well as the
preservation of their biological diversity is a
global problem of modern biology and ecology.
They deplete plants and reduce yields by feeding
on the sap of their generative organs and seeds.
The most dangerous pests of agricultural crops
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Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
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belong to the family’s plant bugs (Miridae) and
shield bugs (Pentatomidae), [2].
The plant bugs (Miridae) are the largest family
of true bugs (Hemiptera: Heteroptera), comprising
nearly 10 000 described species in approximately
1400 genera, [3]. In China, more than 20 species
of mirid bugs have been detected in cotton. Mirid
bugs are polyphagous insects with more than 200
species of host plants, including cotton, Chinese
date, grape, apple, pear, peach, and many other
crops, [4]. Plant bug Apolygus lucorum alone is
held responsible for cotton yield losses of up to
2030% every year. The main control measures
for Apolygus lucorum in cotton fields in China
include chemical control, cultural control (e.g.,
intercropping with trap crops), physical control
(e.g., light traps and sticky traps), and
biological control (e.g., releasing parasitic wasps
and conserving and utilizing natural enemies).
The purpose of reducing the damage of A.
lucorum on cotton yield in China is the highest
results were achieved by chemical treatment with
neonicotinoids of seeds, [5].
Within the Miridae and Pentotomidae families
there is enormous variation in diet and feeding
behavior, including species that are major crop
pests as well as important predators of crop pests,
[6]. Several predatory mirids have been used as
biological controls for pest control, while some
omnivorous species have been considered both a
pest and an important predator of other pest
species, depending on conditions, [7]. Many
phytophagous mirids are globally important pests
of crops such as cotton, lucerne, soybean,
mungbean, strawberry, sorghum, cocoa, apples
and tea, and these species show enormous
variation in diet, ranging from monophagy to
polyphagy, [8].
Nowadays, in cotton-producing countries, the
species of Creontiades pallidus, Creontiades
biseratense, Creontiades dilutus, Lygus lineolaris,
Lygus hesperus, Lygus dessinus, which belong to
the Miridae family of Creontiades and Lygus
geneus cause serious damage to the cotton crop.
As a result, they cause a 30-50% reduction in
cotton yield and up to 80% in common cotton
cultivation areas, [9]. Goodman (1953),
Creontiades pallidus (Rambus) was extensively
distributed throughout the Anglo-Egyptian Sudan
and it was also recorded in Egypt and the Belgian
Congo as a cotton pest. Stamp reported that crop
losses of up to 54 % have been observed at these
stages (1987) however, according to [10], losses
have been higher (82 %) if the pest damages the
plant during the flowering period. Creontiades
biseratense has been found in the Karnataka,
Tamil Nadu, Andhra Pradesh, and Maharashtra
provinces of the Arabian Sea of India, causing
severe damage to Bt cotton, [11]. As reported by
[12], the mirid bug, C. biseratense incidence on
50 days old cotton crop reached its highest point
during November’s last week (17.2 bugs/10
squares) and thereafter, the population declined.
Observed the infestation of mirid bug, C.
biseratense in an epidemic form in Coimbatore on
Bt cotton hybrids during December 2006, [13].
The Australian cotton industry faces several
problems in fighting against pests. These include
damage from key pests, such as the mirid bug,
Creontiades dilutus. Tarnished plant bug (Lygus
lineolaris) caused significant damage to the cotton
balls in the cotton fields, [14], [15]. Since 2000,
scientists have conducted a lot of research to save
cotton from Creontiades pallidus in south Adana
Province Qukurova Region, Turkey, and south
Sabzevar, Razavi Khorasan Province, Iran, [16].
Nowadays, the broaden of the habitat of the pest is
being observed under the influence of various
ecological factors, [17].
In particular, the migration of pest from
southern to central regions and northern regions
were observed C. pallidus and C. dilitus in
Australia, recpectivly. A survey conducted in
Uzbekistan revealed that agricultural crops were
attacked by 19 species of mirids. The predominant
species on cotton included Adelphocoris
lineolatus (Goeze) Adelphocoris jakovlevi
(Reuter), Lygus pratensis (Linnaeus), Lygus
gemellatus (Herrich-schaeffer), Lygus
rugulipennis (Poppius), Orthotylus flavosparsus
(Sahlberg) and Poeciloscytus cognatus (Fieb).
Field trials indicated different losses in seed
caused by mirids on medium and thin fibre
cultivars, [18], [19].
In particular, Creontiades pallidus, which
penetrated the southern Surkhandarya and
Kashkadarya regions of Uzbekistan from the
Middle East through Turkmenistan in 20002005,
has been harming cotton production for the last 10
years, [20], [21]. The analysis of Surkhandarya
region in the 20162019 study reveals that up to
60% of the cotton crop was lost in some areas.
Creontiades pallidus spread over 143714 hectares
in 2017 and 78500 hectares of cotton in 2019,
resulting in over 10 billion dollars spent on
controlling against it. Today, the development of
effective methods to control the bioecology and
damage of cotton shedder bug, [22].
2 Material and Methods
The research was conducted in 20202022 at the
Scientific Research Institute of Agrotechnology of
Crop Breeding and Breeding in the Surkhandarya
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region. Use of an entomological insect net of 38
cm in diameter to determine and distribute cotton
shedder bug in cotton and alfalfa fields. In this
case, the average number of bugs in 10 pairs of
insect net from five areas of the field was
calculated. In cotton, 10 places (a total of 100
plants) were harvested from 10 places on a 1 m
white cloth (Beat Sheet method) and the average
number of bugs per 100 plants was calculated.
Surkhandarya region accounts for 7% of the
cotton area in Uzbekistan. 8590% of farms in
Surkhandarya region specialize in growing cotton
and grain. It is no secret that Uzbekistan is one of
the world's leading cotton-growing countries,
producing about 3.33.4 million tons of raw
cotton annually. At present, mainly medium-
stapled cotton is cultivated in large areas of the
country, but in the past, the cultivation of fine-
stapled cotton varieties in the southern region -
Surkhandarya region - also played a special role.
More than 315000 tons of fine-fiber cotton is
grown in the CIS countries, 116000 tons in the
United States, 36000 tons in China, 31000 tons in
Israel, 24000 tons in Peru, 295 000 tons in Egypt
and 314000 tons in Australia. As the area of fine-
stapled cotton in the region expands, we have
studied the damage that cotton shedder bugs can
cause to this variety of cotton crop, as well as
chemicals that have high biological effectiveness
in combating it.
The experiments were conducted in the
SP-1607 fine-stapled cotton plant which was
planted in 90 cm rows. The special entomologic
cages (Fig. 1) are 120 cm X 120 cm X 120 cm and
are installed in cotton rows 2 to 5 cm (total 10
pairs) to 25-30 cm tall (Fig.1).
Fig. 1: Special cages set up to study the damage
that bugs do to the cotton crop
The special entomologic cages were surrounded
by a small poor cloth, and a special entry to put
bug inside was placed on one side to examine the
damage. Adult bugs were placed on each bale at a
ratio of 0 (control) 10, 30, 50 (early), and 0
(control), 3, 5, and 10 in cultivation late time of
the plant. The damage to the cotton crop of cotton
shredder bug (Creontiades pallidus), alfalfa bug
(Adelphocoris lineolatus) and plant bug (Lygus
pratensis) was calculated as a control.
3 Results
3.1 Monitoring of the True Bugs
Distributed in the Cotton Fields of
Uzbekistan
The monitoring of the species composition of
heteropteras distributed in the cotton fields was
carried out in Surkhandarya, Kashkadarya,
Navoiy, Bukhara, Tashkent, Ferghana regions,
and Karakalpakistan during the years 2020-2022.
The scientific significance of these studies is to
develop effective control measures for cotton
agrobiocenosis, and prevent the spread of harmful
species and damage to other regions.
According to the results, 15 types of bugs were
found in the cotton agrobiocenosis, 6 of which
were phytophagous (Adelphocoris lineolatus,
Creontiades pallidus, Lygus gemellatus, Lygus
pratensis, Orthotylus flavosparsus, Eurystylus
bellevoyei, Trigonotylus ruficornis, Dolycoris
baccarum), 3 zoophaguous (Orius niger, Nabis
palifer, Geocoris after) and 4 zoophytophagous
(Campylomma diversicorne, Campylomma
verbasci, Psallus cognatus, Deraeocoris
punctulatus) (Table 1).
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Table 1. The distribution of bugs by species in the
cotton agrobiocenosis in the regions of our
republic
Species of
bugs
Karakalpakista
n
Surkhandarya
Bukhara
Navoiy
Tashkent
Ferghana
Adelphocori
s lineolatus
++
+
++
++
+
++
+
Creontiades
pallidus
-
++
+
+
+
-
-
Lygus
gemellatus
+
+
++
++
++
++
Lygus
pratensis
++
+
++
+
+
++
Orthotylus
flavosparsus
+
+
+
+
+
+
Campylomm
a
diversicorne
++
++
+
++
++
++
++
Campylomm
a verbasci
+
++
+
++
+
+
+
Trigonotylus
ruficornis
+
Eurystylus
bellevoyei
-
+
-
-
-
-
Dolycoris
baccarum
+
-
-
-
++
-
Psallus
cognatus
-
++
+
+
+
+
Deraeocoris
punctulatus
++
++
++
++
++
++
Orius niger
*
++
+
++
+
++
+
++
+
++
+
++
+
Nabis
palifer *
+
+
+
+
+
+
Geocoris
after*
+
+
+
+
+
+
Note: +- less common, ++-moderately common, +++-
common, *- predator bugs
As a result of the research, in the season of 2022,
Eurystylus bellevoyei, belonging to the Miridae
family, was identified for the first time in Angor
district, Surkhondarya region in the coordination
372456.63". N, 670945.68" E. In Uzbekistan
(Fig.2).
Fig. 2: Eurystylus bellevoyei, a new species for
Uzbekistan
In our republic Lygus pratensis in the northern
regions, Adelphacoris lineolatus in the central
regions, and Creontiades pallidus (cotton bug) in
the southern regions dominate the harmful
phytophagous species and they were 90-95% in
cotton compared to other species. During the
years 2016-2019, it was observed that the cotton
bugs spread mainly in the southern Surkhandarya
and partly in the Kashkadarya regions of
Uzbekistan. In the course of our research in 2020,
for the first time, the cotton bug was found at an
altitude of 306 m above sea level in Qorovulbazar
district of Bukhara region at the coordinates
39°33'3,47"С, 64°47'43,12"В and in Kyziltepa
district of Navoi region, it was found to be
distributed at the coordinates 39°33'3,47"С,
64°47'43,12"В at an altitude of 238 m above sea
level. This indicates that the Creontiades pallidus,
which has been spreading widely in Uzbekistan in
recent years, has adapted to the natural climatic
conditions of Uzbekistan and is increasing its
distribution area (Fig.3).
1 2
Fig. 3: Distribution map of Creontiades pallidus
(1) in Bukhara and Navoi regions (2).
A similar situation was previously observed in
other pests, such as the melon fly and the
mulberry moth. On the one hand, this means that
the Creontiades pallidus is in danger of spreading
to all regions of Uzbekistan, and on the other
hand, it may not spread widely throughout
Uzbekistan due to the fact that it is a species
adapted to live only in the southern (desert)
regions, based on the biology of the insect. In
general, by today, the spread of Creontiades
pallidus is observed in 4 regions of Uzbekistan,
mainly in Surkhandarya, Kashkadarya, and
partially in the desert districts of Bukhara and
Navoi regions near the Todakol reservoir (Fig. 4).
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Fig. 4: The spread of Creontiades pallidus
Uzbekistan
3.2 The Development Dynamics of the
Main Harmful Species of Bug
In the conditions of Uzbekistan, the study of the
development dynamics of the main harmful
species of bugs was carried out in the southern
regions. The first issue was to study the
development and quantity of bugs from the
appearance of the first species of alfalfa, field, and
Creontiades pallidus, which emerged from the
winter, until the end of the season, in crops other
than weed, alfalfa, and cotton. The obtained
results were scientifically analyzed at the end of
the season. According to the results, in the
conditions of the southern districts of
Surkhandarya region, the migration of the
Creontiades pallidus to the cotton fields from the
weeds scattered around the field (Glycyrrhiza,
Alhagi, Medicago) and from alfalfa and other
cultural plants planted in the plots of the
population is observed from the second decade of
May. The number of bugs corresponded to an
average of 1-2 pieces per 10 pairs of movements
of the entomological brush.
During our observations, the first-generation
larvae of the Creontiades pallidus began to appear
in the second decade of June. The maximum
increase in the number of cotton bugs in cotton
corresponded to the third decade of July and the
first decade of August when its average number
increased to 25-30 per 10 plants. Later, after the
defoliation of cotton in September, the number of
cotton bugs decreased sharply (on average 3-5 per
10 plants) due to unfavorable conditions for the
development of cotton bugs in the cotton fields.
In the cotton agrocenoses of the northern
districts of Surkhandarya region (Shorchi, Denov,
Sariosiyo, Uzun), it was observed that the dates
and quantity (number) of the Creontiades pallidus
were significantly different from those of the
southern districts. In the northern regions, the
initial appearance of the Creontiades pallidus was
observed from the third decade of June, when
their number was 2-3 per 10 pairs of movements
of the entomological brush. Later, their number in
the cotton was observed to increase, reaching 20-
25 in 10 bushels of cotton at the end of July and
the beginning of August.
In general, the emergence of bugs from
wintering coincided with March-April, when they
were observed to develop in the surrounding
weeds and early cultivated crops. Their transition
to cotton corresponded to the period of formation
of the generative organs of cotton, i.e. May-June.
This is the time when the second generation of
bugs in nature develops. This year, it was
observed that the bugs left wintering early. After
leaving wintering in June 2021, the first
generation of larvae began to emerge in cotton in
July. We made calculations comparing the
number of bugs leaving wintering and the number
of encounters in previous years. It was observed
that the 2022 Creontiades pallidus came out of
wintering early, and its number was large. It can
be seen that 2021 came out of wintering later than
2020 and encountered very little (Fig. 5).
Fig. 5: Development dynamics of Creontiades
pallidus between 2020-2022 y. in the South of
Uzbekistan
The spread of Adelphocoris lineolatus in northern
districts was observed 15-20 days before cotton
bugs. However, it was observed that the number
of Adelphocoris lineolatus in cotton during the
season in northern and southern districts is
significantly less than that of cotton bugs, i.e., it
does not exceed 1-2 in 10 plants on average. The
main reason for this is that the Adelphocoris
lineolatus is considered an phytophagous insect
and has tropical contact with plants belonging to
the leguminous family. The number of Lygus
protensis in cotton is significantly less than that of
cotton bugs, and only in the northern districts, it is
slightly more common than Adelphocoris
lineolatus.
In the course of our research, we studied the
development levels of all three bug species in
agricultural crops (Phaseolus aureus, Phaseolus,
Zea mays, Medicago, Panicum) that develop
before moving to cotton, and in weeds around
0
10
20
30
40
50
60
70
80
90
100
III III I II III I II III I II III I II III
April Маyjune july Аugust
2020 2021 2022
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cotton. According to the obtained results, it was
observed that from the first decade of April, from
the period of wintering, weed bugs were found in
weeds scattered among fields, ditches, and winter
wheat, and in alfalfa plants planted in residential
plots.
All species of bugs that winter in the form of
eggs was initially found in the above-mentioned
places and plants. From the 3rd decade of April,
the adult varieties of alfalfa bugs began to be
found in the alfalfa field in very small quantities
(an average of 5-7 pieces).
In early May, the first generation of
herbivorous bugs began to breed en masse around
the fields, ditches, and alfalfa plots. During this
period, the average number of alfalfa bugs was
25-30, field bugs were 8-10. In the southern
districts of the Surkhandarya region, Creontiades
pallidus was observed almost a month earlier than
in the northern districts, and it was observed in
small numbers (1-2 units) from the second decade
of April.
The mass reproduction of the Adelphocoris
lineolatus was observed at the end of June and the
beginning of July, and the average number in 10
pairs of movements of the entomological brush
reached 90-100. Unlike Adelphocoris lineolatus,
the maximum number of the Creontiades pallidus
occurred at the end of July and the beginning of
August, and it was 35-40 on average, while the
maximum number of field bugs was found in the
second decade of June, and it was 15-20 on
average. While the number of alfalfa and field
bugs is observed to decrease sharply by the
autumn months, the number of cotton bugs was
found to be more than other bugs in our
observations.
In general, the release of bugs from wintering
coincides with March-April, and at this time, it
was observed that they develop in the surrounding
weeds and early cultivated crops. Their transition
to cotton corresponded to the period of formation
of cotton's generative organs, i.e. June. This is the
time when the second generation of bugs in nature
develops. But later, if we observe their
distribution in cotton, we can see that the
Creontiades pallidus develops in more numbers
than other species. Taking this into account, we
have carried out special calculations to study the
ratio of these three species in the cotton field.
Experiments in this regard were conducted in the
southern regions of our republic in the conditions
of Surkhandarya and Kashkadarya (Karshi,
Nishon districts), and in the northern regions of
Tashkent and Fergana regions. In this case, 100
cotton bugs were collected from the cotton fields
grown in the researched regions using an
entomological comb, and the percentage
differences of all three species were calculated.
According to the obtained results, it was found
that in the southern regions of Uzbekistan, the
largest amount was occupied by Creontiades
pallidus - on average 90-95%, Adelphocoris
lineolatus 0.5-1.0%, Lygus protensis 4.0-8.0%.
3.3 Determining the Damage Caused by
Herbivorous Bugs to the Cotton Crop
More than 25 percent of the world's cotton, that is,
about 6.5 million tons of cotton per year, is grown
in China. More than 100 000 farmers work for
this, and it is worth noting that China has been
able to achieve high efficiency in this regard in a
very short time. Today, Uzbekistan ranks sixth in
the world in terms of cotton cultivation, after
China, India, the USA, Pakistan, and Brazil.
Currently, an average of 1.1-1.2 million tons of
cotton is harvested throughout the republic (5-6
million tons were harvested during the USSR).
Cotton is the main export product of our republic.
Also, in our country, three types of valuable
products are produced from cotton raw materials,
that is, raw materials for textile products - fiber,
oil for food, and animal feed. However, in recent
years, due to drought, environmental factors, and
pests, cotton cultivation is becoming more
complicated. In particular, the impact of harmful
weeds on the yield and quality of cotton is
increasing (Fig.6).
Fig. 6: External and internal views of a cotton
plant affected by Creontiades pallidus.
Determining the possible damage caused by
cotton bugs to the cotton crop is of great practical
importance. In the 2020-2022 season, we
conducted research aimed at studying the damage
caused by cotton bug species to the cotton crop in
the conditions of Uzbekistan.
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The research was carried out on 20 hectares of
cotton fields at the Surkhandarya experimental
station of the Scientific Research Institute of
Agrotechnology of Cotton Breeding, Seeding and
Cultivation (SRI ACBSC). Experiments were
carried out on medium-fiber “UzPITI-1604” and
fine-fiber “SP 1607” varieties of cotton planted
between rows of 90 cm. First, special tents with a
height and width of 120 cm were prepared for the
experiments. Tents were installed in two rows
during the formation of the elements of the cotton
crop before the period of migration of the cotton
fields. In all the tents, 5 rows of 10 bunches of
cotton were left in two rows, and they were
surrounded by a net with a small mesh that the
bugs could not penetrate. A special opening and
closing place was left on one side of the tents to
specially insert the handcuffs and monitor the
damage levels of the cotton crop. Cotton crop
elements (cotton flower, comb, and boll) are
opened on one side of the cages to study the
degree of damage caused by bollworms.
The place (lock, door) is set. The damage
caused by the plant bugs to the cotton crop was
calculated in each decade of the month compared
to the control option (cages installed without the
plant bugs).
3.4 Identify the Damage Caused by Cotton
Bugs to Medium Fiber Cotton Variety
(Gossypium hirsutum)
In the area taken for the experiment (in the tents),
the density of cotton seedlings was 55,000 bushels
per hectare. To the tents, the types of plant bugs
(cotton, alfalfa, and field bugs) are distributed in
the proportion of 0.3-0.8-0.5-1.0-1.5 pieces per
bush of cotton (the number of bugs is suitable for
10 cotton bushes), taking into account the spread
over time, we conducted our experiments in
earlier and later periods.
In the experiment, each tent has a special
value, therefore, each tent was numbered and the
classification of the experiment placed inside it
was written down. In the experiments, each option
was carried out in 3 replications, and the plants of
the control option were left clean (without pests).
During the season, every ten days, the appearance
of crops, damage, spillage, and the opening of
pods were calculated, and the biological
productivity was concluded.
In the first experiment of the first option
conducted in the ratio of 1:1 (10 specimens of
bugs per 10 cotton plants) of alfalfa and field
bugs, there was a decrease of 69.9% of cotton
bolls and flowers, and - 41.2% of cotton bolls
compared to the control options. The second
option for alfalfa bugs, i.e., in experiments with
15 bugs for 10 cotton plants, it was found that the
number of cotton stalks and flowers decreased by
82.2%, and the number of bolls decreased by -
21.1% compared to the control. In the end, the
biological productivity obtained from the first and
second harvests compared to the control in 1/ha
centner was -9.6 c/ha (-32.3%) in the 1:1 ratio
experiment, and the yield obtained from the 1:1.5
ratio experiment compared to the control options
was -10.8 c/ha or -36.4% less compared to the
obtained yield. The same experiment was carried
out simultaneously in the field bugs. In 1:1 ratio
experiments of field bugs, it was observed that
there was a -80.8% reduction of bolls and flowers,
and a -2.6% reduction of cotton bolls compared to
the control options.
The second option for field bugs, i.e., in
experiments with a cotton ratio of 1:1.5, the cotton
grew by +12.5 cm compared to the control, the
number of bolls and flowers decreased by -91.8%,
and the number of pods decreased by -4.4%. At
the end of the field experiments, the biological
yield obtained from the first and second harvests
compared to the control in 1/ha centner was - 2.6
c/ha (-8.6%) in the 1:1 ratio experiment, in the
1:1.5 ratio experiment it was determined that the
yield was -4.0 c/ha or - 13.5% less than the yield
obtained from the control variants.
In the conditions of the Surkhandarya region,
in the cotton agrocenoses, the spread of the cotton
bugs in comparison to other herbivorous plants
and its appearance in different periods in the
northern and southern districts was observed.
Based on the above circumstances, we carried out
the cotton bugs in early and slightly later periods
and greater proportions (1:0.3, 1:0.8, 1:1 until the
end of the season, 1:1 within a month, 1:1.5). We
have also studied the possible damage of this type
of cotton bugs to the cotton crop due to the
expansion of thin fiber cotton fields in
Surkhandarya region in recent years.
In an experiment conducted on June 30th of
cotton bugs in the medium-fiber cotton variety at
a ratio of 1:03 (3 bugs per 10 bushels of cotton),
by August 29, compared to the control, it was
observed that the length of the cotton increased by
+14.9 cm, nodes, and flowers -61.6%, bolls -
51.8% compared to the control. At a ratio of 1:08,
the height of cotton increased to +15.2 cm, the
number of nodes and flowers decreased by -
71.2%, and the number of bolls decreased by -
62.3%.
At the end of the experiments carried out for
cotton bugs, as in the case of alfalfa and field
bugs, in comparison with the first and second
harvest control, in the experiment it was found
that the yield decreased by -18.3 c/ha (by -61.6%)
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DOI: 10.37394/232015.2023.19.29
Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
E-ISSN: 2224-3496
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at a ratio of 1:0.3, by -19.8 c/ha (-66.7 %) at a
ratio of 1:0.8 and by -23.2 c/ha (-78.1) at a ratio of
1:1 (until the end of the season), -21.2 c/ha. When
this ratio is carried out for one month, the
decrease was 21,2 c/ha (-71,4 %), this ratio in
later experiments was 11.3 c/ha (-38.0 %), in the
1:1.5 ratio -26,4 c/ha (-88,9 %), this ratio in later
experiments was 14.8 c/ha (50.2%).
3.5 Identify the Damage of Cotton Bugs
(Gossypium barbadense) to the Fine-Fiber
Cotton Crop
Only Lygus protensis, Adelphocoris lineolatus are
included in the list of pests of a cotton plant in the
Republic of Uzbekistan. Several local scientists
have conducted scientific research on the damage
and control system of these plant bugs species to
cotton. It is known that all pests are combated
only when they reach the Economic Injury Level.
In all the old literature available to us, it was
stated by local scientists that it is necessary to
fight against Adelphocoris lineolatus only when
there are 100-150 cotton bolls per 100 cotton
plants, and this was followed. However, in recent
years in the south of our republic, a new species
of plant bugs (Creontiades pallidus) appeared in
the cotton fields and began to cause great damage.
Based on old data, agricultural experts used to
control Creontiades pallidus in cotton fields only
when there were 100-150 plants per 100 cotton
plants, resulting in major crop losses was
observed. Today, we conducted our scientific
research in order to study the level of damage to
the cotton crop when there are 100 or more
bollworms per 100 cotton plants.
The study of the damage of cotton bugs to the
fine-fiber cotton crop was carried out at two ratios
of 10:10 (10 bugs per 10 plants) and 10:15. The
experiments were conducted in the third decade of
June. Spills of cotton lye elements (boll, flower)
lyre by cotton handcuffs were calculated every 10
days against control. Prior to the experiments, the
combs and flowers were made of cotton elements
in each ratio at almost the same rate of 10x10,
10x15, and in the control, respectively, at 6.7-7.2-
7.0, and the cotton stalks at 1.3-1.1-1.0. A sharp
decrease in cotton yield was observed by
handcuffs every 10 days compared to the control.
Two months later, the experimental cotton stalks
and flowers were placed in both ratios at a rate of
79.5% in the 10x10 ratio and 89.7% (0.8-0.4-3.9)
in the 10x15 ratio, a decrease of 59.6% (9.4-9.2-
22.4) was observed (Table 2).
Table 2. Effect of the yield of fine-stapled cotton
on a cotton shaft on yield Southern Uzbekistan,
Surkhandarya region, 2020
Cotton-
bugs
Number of flowers and stems per plant
ratio
20,1
30,1
10,1
22,1
28,1
17,1
29,1
10:10
6,7
12,3
10,6
2,1
1,5
1
0,8
10:15
7,2
13,1
10,5
2
0,5
0,1
0,4
Control
7
13,2
13,4
9,9
9,6
8,4
3,9
The average number of cotton balls per plant
20,1
30,1
10,1
22,1
28,1
17,1
29,1
1,3
4,9
9,5
12,4
9,4
9,5
9,4
1,1
3,9
8,1
10,2
9,3
9,1
9,2
1
4,3
8,5
13,1
14,5
20,2
22,8
The difference from control
Control
Bud, difference in flower, %
10:10
6,8
20,9
78,8
84,4
88,1
79,5
10:15
0,8
21,6
79,8
94,8
98,8
89,7
Control
-
-
-
-
-
-
Difference in balls,%
-
12,2
10,5
5,3
35,2
53
58,8
-
9,3
4,7
22,1
39,9
55
59,6
-
-
-
-
-
-
-
At the end of the experiments, the cotton fiber in
all tents was harvested in late September and mid-
October and calculated for control. Cotton yields
were found to be - 14.7 c/ha (55.5%) and - 17.2
(65.3%) loss, respectively, compared to the
control in the 10 x 10 and 10 x 15 ratios with the
plant.
3.6 Identify the Effect of Insecticides
against Bugs
The main sucking insect pests of cotton belong to
the orders Hemiptera and Thysanoptera, and
include aphids, leafhoppers, silverleaf whitefly,
sucking bugs (mirids, green vegetable bugs), and
thrips, [23]. In China, mirid bugs were the
primary pests after the adoption of Bt cotton and
the subsequent reduction in insecticide used to
manage H. armigera. In addition to mirid bugs,
the number of other sucking pests, such as aphids,
mealy bugs, planthoppers, and silverleaf
whiteflies, increased about three years after the
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Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
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introduction of Bt cotton, [24]. In Australia, the
importance of the green vegetable bug Nezara
viridula L. and the green mirid Creontiades
dilutus (Stål) have increased since the adoption of
Bt cotton. Studied the bioefficacy of insecticides
against mirid bug C. bisertense in irrigated Bt
cotton and reported that fipronil 5 SC @ 25 g
ai/ha was recorded lowest mirid population
(0.52/15 square) with the highest yield (34.31
q/ha), [25], [26].
Suggested a similar approach that 32 Bt and
non-Bt cotton hybrids against mirid bug incidence
was recorded on five squares from the top canopy
of each plant. It was also reported that NCHB-990
recorded the least number of mirid bug (5.30
mirid/5squres) of all hybrids. However, non Bt
hybrid DCH-32 and DHB-105 recorded a high
incidence of mirid bug (11.5-11.2 mirid/5
squares). Whereas, shedding varied, with least
being observed on MRC-6918 followed by DCH-
32, [8].
The bio-efficacy of certain insecticides
against mirid bug, P. biseratense and the
economic feasibility were also studied by B.
Prajna Devaiah et al., in Mandya city of India.
Their studies showed that among nine insecticide
molecules tested for their bio-efficacy against
mirid bug, the seed treatment along with foliar
sprays of imidacloprid 60 FS and thiamethoxam
25 WG @ 0.3 g/l found to be effective and this
was followed by flonicamid 50 WG @ 0.4 g/l,
imidacloprid 60 FS + acetamiprid 20 SP @ 0.3 g/l
and clothianidin 50 WDG @ 0.1 g/l, [22].
Lygus protensis and Adelphocoris lineolatus
were considered the main pests of cotton fields in
Uzbekistan. Chemical preparations recommended
for all sucking pests of cotton (aphid, thrips,
spider mite, spider mite) are used in the fight
against them. The effectiveness of chemical
preparations has given the intended result.
However, in recent years, in the south of our
republic regions (mainly desert areas) in the
cotton fields, the species Creontiades pallidus,
introduced from neighboring countries, began to
spread widely and cause great damage. Cotton
farmers have been fighting Creontiades pallidus
with chemicals used in other regions to control
Lygus protensis and Adelphocoris lineolatus and
have not achieved the expected positive results.
To determine the cause of the above problem,
we studied the biological effectiveness of several
classes of chemical preparations against
Creontiades pallidus.
In our research, we studied the effectiveness of
several chemical drugs against phytophagous
bugs, which are causing great damage to the
cotton crop today. 300 liters of working fluid
(Water) per hectare were used for processing
using an OVX-600 tractor sprayer. Calculations
were made on pretreatment and posttreatment
days, and efficacy was calculated using Abbot's
formula, which provides a control option.
In the experiment, 7 drugs that have been
proposed to combat the pests of cotton in recent
years in Uzbekistan were tested (Table 3).
Table 3. Biological efficacy of insecticides against
Creontiades pallidus in cotton plants
Variants
Active
substance
Drug
use,
kg, l/hа
Transform,
50%.w.s.g.
sulfoxaflor
0.15
Lead, 5% w.s.g.
pymetrozine
0.2
Ribo super, 25% s.c
chlorpyrifos
2.0
Imido, 35% s. c
imidocloprid
0.135
Safegor, 40% e. c
dimethoate
1.0
Malation, 57% e. c
malathion
0.6
Sumi alfa, 20% e. c
esfenvalerate
0.1
Control (without
insecticides)
-
-
As a result of experiments, Transform, Transform,
50% water soluble granules (active substance
sulfoxaflor) had a satisfactory effect of 89.8-92.5-
77.6% at a rate of 0.15 kg/ha, Safegor, Safegor,
40% emulsion concentrate (98.3%) and Ribo
Super, 25% suspension concentrate (93.4 %) had
a good effect. Lead, 5% water soluble granules
had 59.0-31.8%, Imido, 35% suspension
concentrate had (18.9%), Malation had 73.4-
58.8%, Sumi alfa had 66.4-20.3% unsatisfactory
results, taking into account the high damage of
boll, this result will not be sufficient (Fig.7).
Fig. 7: Biological effectiveness of chemical
preparations against harmful Creontiades pallidus
As a result of the scientific research
conducted to determine the effectiveness of
chemical preparations against Creontiades
pallidus, we were convinced that this type of plant
bugs is more resistant to drugs than other plant
0
20
40
60
80
100
Percent, %
Biological efficacy, %
1 day
4 day
8 day
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Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
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bugs (Lygus protensis, Adelphocoris lineolatus).
Since this plant bugs population is resistant to
chemical preparations belonging to the
organophosphorus class, the biological
effectiveness of Transform 50%, Ribo Super 25%,
and Safegor 40% drugs showed high results. On
the other hand, Creontiades pallidus showed low
efficiency due to strong resistance to pyrethroid
and neonicotinoid chemicals (Imido, 35%, Sumi
alfa, 20%). From this, it can be concluded that in
the southern regions of the republic where
Creontiades pallidus is spread, it is impossible to
fight with complex chemical preparations against
all sucking pests. In farms, it is necessary to fight
against them with chemical preparations
belonging to the organophosphorus class, which
have been highly effective in separate tests.
4 Conclusion
As a result of the conducted research, 15 species
of cotton bugs were identified in the cotton fields
of Uzbekistan, of which the species Eurystylus
bellevoei was identified for the first time. It was
determined that the yield of alfalfa (A. lineolatus)
decreases by 32.3-36.4%, and by 8.6-13.5%, when
there are 100-150 bugs per 100 cotton plants
during the cotton picking period. If cotton is
infected with cotton bugs (C. pallidus) in the early
period (June), the yield of cotton decreased from
61.6% to 88.9%, if there are 30 to 150 bugs per
100 cotton plants, and if it is infected later (July-
August) a decrease from 38.0 to 50.2% was
observed. If fine fiber cotton is damaged by cotton
bugs (100-150 specimens per 100 bushels) during
the vegetation period, the cotton yield is reduced
by 55.5-65.3%.
The obtained results show that in our republic,
agricultural experts fight against bollworms based
on old data, i.e. not when there are more than 100
bollworms per 100 cotton bushes, but when they
first appear in small numbers in the fields, will
have to fight against.
The most effective drugs against heteroptera
are: Safegor, 40% emulsion concentrate (98.3%),
Ribo Super, 25% suspension concentrate (93.4%),
Transform, 50% water soluble granules (92.5%),
and Mosetam 20 SP (82.8-81.9%). Arvilmek 1.8
EC (active substance- abamectin), Lead, 5% water
soluble granules (active substance-pymetrozine),
Imido Star, 20% suspension concentrate (i.e.
imidacloprid) were found to have unsatisfactory
(below 70.0%) results against cotton heteropteras.
Based on the obtained results, it is not
possible to fight with complex chemical
preparations against all sucking pests in the
areas where Creontiades pallidus is spread in
the south of Uzbekistan. In farms, it is
necessary to fight against them with chemical
preparations belonging to the
organophosphorus class, which have been
highly effective in separate tests.
Acknowledgments:
We express our gratitude to Konstantinov Fedor
Vladimirovich, a researcher at the Institute of
Zoology of the Russian Academy of Sciences,
who closely helped in identifying a new species of
Eurystylus bellevoyei for the fauna of Uzbekistan.
We also thank the Committee on Ecology and
Environmental Protection of Karakalpakstan and
Surkhandarya for their close cooperation. Institute
of Zoology, Academy of Sciences of the Republic
of Uzbekistan for permission of using true bugs
collection in the Department of Zoological
collection of the institute.
References:
[1] Devaiah, B. P., Kumar, L. V., Sunil, K., &
Manjunath, G. Bio-efficacy of selected new
insecticides against mired bug
Poppiocapsidea biseratense (Distant) and
cost economics of mirid bug management in
sesame. International Journal of Chemical
Studies, 8(4), 2020, pp.144150.
doi.org/10.22271/chemi.2020.v8.i4c.9881
[2] Akbar, W. A new transgenic trait protects
cotton from thrips and Lygus damage.
International Congress of Entomology., 2016.
doi.org/10.1603/ice.2016.112914
[3] Cassis, G., & Schuh, R. T. Systematics,
Biodiversity, Biogeography, and Host
Associations of the Miridae (Insecta:
Hemiptera: Heteroptera: Cimicomorpha).
Annual Review of Entomology, 57(1), 2012,
pp. 377404. doi.org/10.1146/annurev-ento-
121510-133533
[4] Zhang, Z., Wang, Y., Zhao, Y., Li, B., Lin,
J., Zhang, X., Liu, F., & Mu, W. Nitenpyram
seed treatment effectively controls against the
mirid bug Apolygus lucorum in cotton
seedlings. Scientific Reports, 7(1). 2017,
doi.org/10.1038/s41598-017-09251-9
[5] Jiang, Y. Y., Lu, Y. H. & Zeng, J. Forecast
and management of mirid bugs in multiple
agroecosystems of China. China
Agriculture Press: 2015, pp. 9298.
[6] Meisner, M. H., Zaviezo, T., & Rosenheim,
J. A. Landscape crop composition effects on
cotton yield, Lygus hesperus densities and
pesticide use. Pest Management Science,
WSEAS TRANSACTIONS on ENVIRONMENT and DEVELOPMENT
DOI: 10.37394/232015.2023.19.29
Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
E-ISSN: 2224-3496
338
Volume 19, 2023
73(1), 2016, pp.232239.
doi.org/10.1002/ps.4290
[7] Saeed, R., Razaq, M., & Hardy, I. C. W. The
importance of alternative host plants as
reservoirs of the cotton leaf hopper, Amrasca
devastans, and its natural enemies. Journal of
Pest Science, 88(3), 2014, pp.517531.
doi.org/10.1007/s10340-014-0638-7
[8] Rohini & Mallapur, C.P. Reaction of
cultivated Bt cotton hybrids to mirid bug,
Creontiades biseratense (Distant) (Miridae:
Hemiptera). Karnataka Journal of
Agricultural Sciencis. - India. 23(1): 2013,
pp.133-134.
[9] Cappadonna, J. K., Miles, M. M., Hereward,
J. P., & Walter, G. H. Invasions of green
mirid (Creontiades dilutus) (Stål)
(Hemiptera: Miridae) into cotton
perceptions of Australian crop consultants.
Agricultural Systems, 166, 2018, Pp.7078.
doi.org/10.1016/j.agsy.2018.07.017
[10] Abdulla Iskandarov, Lola Gandjaeva,
Dilshod Musaev, Gulnara Mirzayeva,
Bakhtiyor Kholmatov, Hasan Jumanazarov,
Aygul Jangabaeva, Kahramon Razzakov,
Ulmasbek Abdullaev, Ikram Abdullaev.
Updated Checklist of the Pentatomidea
(Heteroptera: Pentatomomorpha) of
Uzbekistan. Wseas Transactions on
Environment and Development. Volume 18,
2022., pp. 1283-1295.
10.37394/232015.2022.18.121
[11] Saeed, R., Razaq, M., & Hardy, I. C. W. The
importance of alternative host plants as
reservoirs of the cotton leaf hopper, Amrasca
devastans, and its natural enemies. Journal of
Pest Science, 88(3), 2014, pp.517531.
doi.org/10.1007/s10340-014-0638-7
[12] Hill, L. Migration of green mirid,
Creontiades dilutus (Stål) and residence of
potato bug, Closterotomus norwegicus
(Gmelin) in Tasmania (Hemiptera: Miridae:
Mirinae: Mirini). Crop Protection, 96, 2017,
pp.211220.
doi.org/10.1016/j.cropro.2017.02.006
[13] Efil, L., & Bayram, A. Factors affecting the
distribution of two mirid bugs, Creontiades
pallidus (Rampur) and Campylomma
diversicornis (Reuter) (Hemiptera: Miridae)
and notes on the parasitoid Leophron
decifiens Ruthe (Hymenoptera: Braconidae).
Entomologica Fennica, 20(1), 2009, pp.917.
doi.org/10.33338/ef.84454
[14] Ravi, P. R., Patil, B. V., Narayanaswamy, K.
S., Sowmya, E., Lepakshi, N. M., & Sajjan,
P. S. Biology of mirid bug, Creontiades
biseratense (Hemiptera: Miridae).
International Journal of Bioresource Science,
2(3), 2015, pp.157. doi.org/10.5958/2454-
9541.2015.00011.0
[15] Musaev D., Kholmatov B., Sattarov N.,
Amirov I., Musayeva М. & Abdurakhmonov
Sh. Cotton shredder bug Creontiades pallidus
(Rambur, 1839) damage to cotton crop in
Surkhandara region of South Uzbekistan.
EurAsian Journal of BioSciences. Turkey.
14. 2020, pp. 4683-4687.
[16] Varshney, R., & Budhlakoti, N. Biology and
functional response of the predator, Dortus
primarius (Distant) (Hemiptera: Miridae)
preying on Frankliniella schultzei (Trybom)
(Thysanoptera: Thripidae). Egyptian Journal
of Biological Pest Control, 32(1). 2022,
doi.org/10.1186/s41938-022-00531-9
[17] Oliveira CM, Auad AM, Mendes SM, Frizzas
MR Crop losses and the economic impact of
insect pests on Brazilian agriculture. Crop
Prot. 2014. pp.56:50.
doi.org/10.1016/j.cropro.2013.10.022
[18] Bouagga, S., Urbaneja, A., & Pérez-Hedo,
M. Comparative biocontrol potential of three
predatory mirids when preying on sweet
pepper key pests. Biological Control, 121,
2018, pp.168174.
doi.org/10.1016/j.biocontrol.2018.03.003
[19] Varshney, R., & Budhlakoti, N. Biology and
functional response of the predator, Dortus
primarius (Distant) (Hemiptera: Miridae)
preying on Frankliniella schultzei (Trybom)
(Thysanoptera: Thripidae). Egyptian Journal
of Biological Pest Control, 32(1). 2022,
doi.org/10.1186/s41938-022-00531-9
[20] Ruzmetov, R., Matyakubova, Y., Abdullaev,
I. 2020 Cytosporosis diseases of apple trees
(Reinette Simirenkomalus) and its
distribution in the lower Amudarya region //
nternational Journal of Current Research and
Review, 12 (14), 6267.DOI.
10.31782/IJCRR.2020.121413
[21] Abdullaev U.R., Abdullaev I.I., Gandjaeva L.A.
The Social WASP Fauna of Riparian Tuqai
Forestin Khorezm region Uzbekistan
(Hymenoptera, Vespidae) International Journal of
Current Research and Review Vol 12, Issue 14,
2020, pp. 96-99. DOI:
10.31782/IJCRR.2020.121420
[22] Hosseini, S. M., Asadi, H. B., Kaunail, K.,
Shojaii, M., & Hadiostvan. Study on
bioecology of cotton shedder bug
Creontiades pallidus (Rambur).
(Heteroptera: Miridae) in cotton fields of
Khorassan. Journal of Agricultural Sciencis.
Iran. 8(2), 2022, pp. 910.
[23] Hill, L. Migration of green mirid,
Creontiades dilutus (Stål) and residence of
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Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
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potato bug, Closterotomus norwegicus
(Gmelin) in Tasmania (Hemiptera: Miridae:
Mirinae: Mirini). Crop Protection, 96, 2017,
pp.211220.
doi.org/10.1016/j.cropro.2017.02.006
[24] Musser, F. R. Integrating multiple strategies
for Lygus lineolaris management in cotton.
2016 International Congress of
Entomology.https:doi.org/10.1603/ice.2016.9
3445
[25] Sahana K B, Navi, S., L, V., Kumar C, S.,
Kumar V B, S., G, S., & N M, C. Resistance
to Mirid Bug Creontiades biseratense
(Distant) in Cotton. Indian Journal of
Entomology, 2022, pp. 14.
doi.org/10.55446/ije.2022.671
[26] Rasheed, I. Screening of different
insecticides against Helicoverpa armigera
(Hubner), (Lepidoptera: Noctuidae) and its
effect on yield of tomato crop. Pure and
Applied Biology, 7(4). 2018,
https://doi.org/10.19045/bspab.2018.700208
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en_US
WSEAS TRANSACTIONS on ENVIRONMENT and DEVELOPMENT
DOI: 10.37394/232015.2023.19.29
Musayev Dilshod, Navruz Sattorov,
Jamila Abdullaeva, Musaeva Makhliyo,
Saparov Abdirahman, Bakhtiyor Kholmatov,
Yusupova Asiya, Medetov Maxsetbay
E-ISSN: 2224-3496
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