Journal Pre-proofs Full length article In-vitro assessment of food consumption, utilization indices and losses promises of leafworm, Spodoptera litura (Fab.), on Okra crop Ahmad Nawaz, Habib Ali, Muhammad Sufyan, Muhammad Dildar Gogi, Muhammad Jalal Arif, Abid Ali, Muhammad Qasim, Waqar Islam, Muhammad Tayab, Imran Bodla, Madiha Zaynab, Khalid Ali Khan, Hamed A. Ghramh PII: DOI: Reference:
S1226-8615(19)30477-7 https://doi.org/10.1016/j.aspen.2019.10.015 ASPEN 1463
To appear in:
Journal of Asia-Pacific Entomology
Received Date: Revised Date: Accepted Date:
27 July 2019 17 September 2019 25 October 2019
Please cite this article as: A. Nawaz, H. Ali, M. Sufyan, M. Dildar Gogi, M. Jalal Arif, A. Ali, M. Qasim, W. Islam, M. Tayab, I. Bodla, M. Zaynab, K. Ali Khan, H.A. Ghramh, In-vitro assessment of food consumption, utilization indices and losses promises of leafworm, Spodoptera litura (Fab.), on Okra crop, Journal of Asia-Pacific Entomology (2019), doi: https://doi.org/10.1016/j.aspen.2019.10.015
This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
© 2019 Korean Society of Applied Entomology. Published by Elsevier B.V. All rights reserved.
In-vitro assessment of food consumption, utilization indices and losses promises of leafworm, Spodoptera litura (Fab.), on Okra crop
1 2 3
Ahmad Nawaz1*, †, Habib Ali2*,†, Muhammad Sufyan1, Muhammad Dildar Gogi1, Muhammad
4
Jalal Arif1, Abid Ali1, Muhammad Qasim3 , Waqar Islam4, Muhammad Tayab10, Imran Bodla6,
5
Madiha Zaynab5 , Khalid Ali Khan7,8,9, Hamed A. Ghramh7,8,9
6 7
1 Integrated
8 9
2 Department
Pest Management Laboratory, Department of Entomology, University of Agriculture, Faisalabad, Pakistan of Entomology, University of Agriculture, Faisalabad, Depalpur Campus, Okara,
Pakistan
10
3Institute
of Insect Sciences, Zhejiang University, Hangzhou 310058, P.R. China
11
4Institute
of Geography, Fujian Normal University, 350007, China
12
5College
of life Science, Fujian Agriculture and Forestry University, China
13 14
6Insect
15 16
7 Research
17 18
8 Unit
19 20
9Biology
21
10College
22
†
23 24 25
* Correspondience: A. Nawaz (
[email protected]) & H. Ali (
[email protected])
Biodiversity and Conservation Group, Department of Entomology, Pir Mehr Ali Shah Arid Agriculture University, Rawalpindi, Pakistan Center for Advanced Materials Science (RCAMS), King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia. of Bee Research and Honey Production, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia Department, Faculty of Science, King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia of Crop Science, Fujian Agriculture and Forestry University, China
These authors have contributed equally to this work
26
1
Abstract
27 28
The lepidopteran insect pests have significant importance in vegetable production. The present
29
study was performed to investigate the baseline studies about the assessment of feeding and
30
consumption potential, utilization indices and losses promises of leafworm, Spodoptera litura
31
(Fab.) on Okra. The data regarding feeding potential, food utilization and consumption indices
32
as well as losses of different larval instars were recorded and subjected to appropriate statistical
33
analysis. The results showed that, in the beginning, the approximate digestibility of various
34
instars was increase, e.g. third instar (51.36%-64.03%), fourth instar (63.42%-69.45%) and
35
fifth instar (70.25%-76.10%). However, after a certain period, the digestibility was decreased
36
and efficiency to convert the ingested food into biomass varied significantly. The consumption
37
index values increased with an increase in time but the consumption and growth rate was
38
declined of fourth instar larvae. The ingestion and digestion increased of third (10.01-13.06,
39
8.32-11.91 mg), fourth (11.27-17.28, 10.96-14.03 mg) and fifth (12.60-19.40, 11.93-15.28 mg)
40
larval instars. The corrected weight of consumed leaves increased with a gain in body weight.
41
However, in the third instar, a decline was observed on the last day of feeding. Maximum leaf
42
area was consumed by fifth instar larvae (44.66 cm2) followed by fourth (35.41 cm2) and third
43
(27.98 cm2) instars. In conclusion, all the dependent parameters, including food utilization
44
potential, consumption indices and losses were higher for fifth instar larvae than others. These
45
results emphasized the re-establishment of fundamental (economic threshold level: ETL,
46
economic injury level: EIL) integrated pest management concepts.
47
Keywords: Lepidopteran insect pests; armyworm; okra; feeding potential; ETL; EIC
48
Introduction
49
Okra is native to Africa, North Australia to the Pacific and South-East Asia (Kaleri et al., 2011)
50
and commercially grown in many countries of the world such as Turkey, Bangladesh, Malaysia,
51
Southern United States, Afghanistan, Pakistan, Brazil, Thailand, India, Ethiopia, Iran, Western
52
Africa, Yugoslavia, Japan, Myanmar and Cyprus (Purseglove, 1987; Benjawan et al., 2007;
53
Qhureshi, 2007). In the world, its production is about six million tons per year (Benchasri, 2012).
54
In 2009-2010, the area under okra crop was 0.43 million hectares, and the production stood at 4.54
55
million tons (Benchasri, 2012). India was the first country in the world, with 3.5 million tons of
56
okra production from over 0.35 million hectares of land (FAOSTAT, 2008). India is the most 2
57
important country in the world for okra production and shares a part of 67.1%, followed by Nigeria
58
(15.4%) and Sudan (9.3%) (Varmudy, 2011). In Pakistan, okra crop is planted on an area of 15,081
59
hectares with an annual production of 114,657 tons, and it stands sixth for its okra production
60
(Varmudy, 2011). Okra is a edible crop and mainly grown for obtaining fruits, but other plant parts
61
like leaves, petals, stems, flowers and roots are also used as medicine, bio-fuel and for food purpose
62
in several regions of the world (Aziz et al., 2011). Its nutritive value is higher than tomato, cucurbit,
63
and eggplant, except bitter gourd (Nonnecke, 1989). It contains proteins, carbohydrates and
64
vitamin C (Lamont, 1999; Owolarafe and Shotonde, 2004; Gopalan et al., 2007; Arapitsas, 2008;
65
Dilruba et al., 2009).
66
Okra is susceptible to several diseases and a wide range of insect pests (N’Guessan et al., 1992;
67
Ghanem, 2003) at its various growth stages (Ek-Amnuay, 2010; Fasunwon and Banjo, 2010). One
68
of the major limitations for okra production is heavy infestations of several insect pests (Pal et al.,
69
2013). Avoidable losses due to pests was at about 54% (Chaudhary and Dadheeck, 1989). Insect
70
pests like crickets attack at the seedling stage while the sucking pests are common during the
71
vegetative stage of the crop (Fajinmi and Fajinmi, 2010). Among chewing insects, leafworm
72
Spodoptera litura (Fab.) is the most destructive pest which feeds on early vegetative stages of okra
73
(Kumar et al., 2010). It is a sporadic insect pest that causes 25.8%-100% losses in crops (Dhir et
74
al., 1992), depending upon the crop stage and its infestation level in the field. The major crops
75
attacked by armyworm are brassica, maize, cotton, flax, lucerne, rice, soya bean, tobacco, jute, tea,
76
cucurbit, potato, capsicum, tomato, eggplant (Zhou et al., 2010), cauliflower, okra, cabbage,
77
radish, peanut and other legumes. It feeds gregariously on leaves leaving behind the midribs
78
(Ahmad et al., 2013). It is the most destructive insect pest in the Asia-Pacific region because of its
79
high reproductive potential and massive infestation rates (Ahmad et al., 2013). Eggs are laid in
80
clusters and are covered with the tuft of hair to protect them from more than 100 species of
81
biocontrol agents (Rao et al., 1993). A single female moth can lay more than 2000 eggs in her life
82
span of 6-8 days (Ahmad et al., 2013). The eggs hatch in 2-3 days, and there may be 3-4 continuous
83
layers in a single batch (Waterhouse and Norris, 1987; Hill, 1975.). Although, many biological
84
(Ali et al., 2016, 2108a,b,c,d,e; Arif et al., 2018; Bala et al., 2018; Qasim et al., 2018a,b) and
85
biopesticidal approcehs (Ali et al., 2015; Shakeel et al., 2018) has been made recently against
86
major crop pests.
3
87
But the ever-changing climatic conditions change the behavior of insects, and there is a need
88
to investigate the damaging potential of major insect pests to re-establish the economic injury
89
level and economic threshold levels. Therefore, the present research was planned to investigate
90
the baseline studies about the assessment of feeding potential, food consumption and utilization
91
indices and losses of larval instars of S. litura on okra. This study will help to analyse the
92
impact of recent climatic conditions on the behavior of S. litura in Pakistan.
93
M at er i als an d met hod s
94
Okra cultivar and its cultivation
95
The seed of hybrid variety of okra (Adventena-803) was purchased from ICI-company and used
96
as a target crop. The okra crop was sown at the University of Agriculture Faisalabad as per
97
recommended sowing method (line sowing) and agronomic practices. All the recommended
98
agronomic practices were performed uniformly throughout the growing season of okra. However,
99
no plant protection measures were practiced at least fifteen days before the picking of leaves for
100
offering to armyworm larvae.
101
Preparation of larval culture of Spodoptera litura
102
Leaves with egg-masses of S. litura were clipped from the mung bean field while adult female
103
moths were collected from light sources near the mung bean field. The collected eggs-masses were
104
placed on the moistened filter paper adjusted in petri-dishes till their hatching to get larval instars.
105
Whereas moths were kept captured inside the insects rearing cages having cotton swab soaked in
106
adult moth diet (honey: water: yeast : 1: 9: 1) and folded strips of black colors in hanging position.
107
The egg-masses on the folded strips were scratched and also placed on the moistened filter paper
108
adjusted in Petri dishes till their hatching to get larval instars. The larval culture was maintained
109
in the IPM laboratory at laboratory condition (28 ± 2 ºC, 65 ± 5 % R.H). The newly emerged larvae
110
of third, fourth and fifth instar were kept starved for 12h and then offered okra leaves as the food
111
inside the plastic boxes in the laboratory. The materials that were used in present research include
112
Electrical Balance, Plastic Boxes, Iron Net, Datasheet, Leaf Area Meter.
113
Methodology
114
Four sets, each containing 12 plastic boxes (total 48 boxes), were cleaned and sterilized, and each
115
set was denoted as one treatment. There were four treatments [third instar larvae (T1), fourth instar
116
larvae (T2), fifth instar larvae (T3) and no larvae (T0)] and each treatment was replicated 12 times 4
117
for each larval instar of S. litura. In this way, 48 boxes were arranged in four sets in insect rearing
118
room, maintained at 28 ± 2 ºC, 65 ± 5% R.H and 16h:8h of light and dark period.
119
Ten newly emerged larvae of each (third, fourth and fifth) instar were picked from laboratory
120
culture and released into each of 12 boxes of set-1, set-2 and set-3, respectively. In control
121
treatment (set-4), no larvae were released. After 12 h of starvation in sample size (set-1 and set3),
122
the initial accumulative weight of the ten larvae each replicate of each treatment was measured by
123
weighing balance, and an average weight of larvae was calculated. Fresh, cleaned and sterilized
124
okra leaves were offered as food to the larvae. Before providing these leaves, the initial area and
125
weight of the leaves were measured with the help of leaf area meter and weighing balance,
126
respectively. After 24 h, the old leaves were replaced with the fresh leaves.
127
Similarly, the area as well weight of fresh and consumed leaves were measured before and after
128
consumption, respectively. These observations were recorded daily, and the leaf area consumed
129
per day per larvae was measured. The quantity of food consumed, fecal matter excreted and larval
130
growth was determined based on the fresh and dry weight. In case of control treatment, only fresh
131
leaves after weighing were kept under the same set of condition to determine the natural loss of
132
moisture, which was used for calculating the corrected weight of consumed leaves by equitation
133
described by Ghanema (2002).
134
Corrected weight of consumed leaves = (Cb / Ca) × Ta
135
Where: Cb = Initial fresh weight of leaves without larvae; Ca = Final weight of leaves without
136
larvae; Ta = Final weight of leaves with larvae after feeding
137
In the rest of the treatments (set-1 to set-3), the weight of leaves before offering and after
138
consumption was determined daily. Amount of food ingested was calculated by subtracting the
139
weight of residual leaves from weight of leaves given as wet and dry matter. The food digested
140
was calculated by subtracting the weight of fecal matter produced from the weight of food ingested.
141
The samples of leaves, faeces and larvae were dried in the oven at 80゚C to a constant weight. The
142
leftover food and faeces were recorded and removed daily. Thus, for each instar, the increase in
143
fresh and dry weights of larvae, fresh and dry weights of food eaten and digested and dry weight
144
of faeces were recorded (Rath et al., 2003; Seidavi, 2009). Fresh leaf mass (L1), consumed fresh
145
leaf moisture as well as weight and moisture of faeces and un-used leaves (L2) was measured
146
carefully and recorded daily. The actual leaf mass-consumed was calculated using the following
147
formula: 5
148
Leaf-mass consumed = [L1 × moisture (%)]–[L2 × moisture (%)]
149
Various indices of food consumption and utilization were determined by the following
150
methods/formulae described by Waldbauer (1968), Rath et al. (2003) and Seidavi (2009).
151
Approximate Digestibility (AD) =
152
Efficiency of conversion of ingested food to biomass (ECI) =
153
Efficiency of conversion of digested food to biomass (ECD) =
154
Consumption Index (CI) =
155
Growth Rate (GR) =
156
Where: G = Fresh weight gain of larvae; C = Fresh weight of consumed leaves; F = Feces weight
157
during feeding; T = Duration of feeding period; A = Mean fresh weight of larvae during feeding
158
The whole of the experiment was laid out in CRD (completely randomized design) with twelve
159
replications and four treatments.
160
Statistical Analysis
161
The data regarding indices mentioned above of food consumption and utilization were transformed
162
and then analyzed using the ANOVA technique. The means were grouped and compared using
163
Tukey HSD test using suitable statistical software package.
164
Results
165
Table 1 showed analysis of variance of data regarding the dependent parameters (Quantity of food
166
ingested (mg), quantity of food digested (mg), efficiency of conversion of ingested food into
167
biomass (%), efficiency of conversion of digested food into biomass (%), corrected weight of
168
consumed leaves (mg), approximate digestibility (%), consumption index (mg), growth rate (mg)
Dry weight of food eaten ― Dry weight of faeces produced × 100 Dry weight of food eaten Dry weight gain of larvae × 100 Dry weight of food eaten
G × 100 C―F
C T×A
G T×A
6
169
and consumed leaf area (cm2)) by third, fourth and fifth instar larvae of armyworm (S. litura) after
170
24h, 48h and 72h, respectively. Analysis of variance parameters reveal that dependent variable
171
(Quantity of food ingested (mg), quantity of food digested (mg), efficiency of conversion of
172
ingested food into biomass (%), efficiency of conversion of digested food into biomass (%),
173
corrected weight of consumed leaves (mg), approximate digestibility (%), consumption index
174
(mg), growth rate (mg) and consumed leaf area (cm2)) varied among different treatments (third,
175
fourth and fifth larval instar) as (P < 0.05).
176
The fifth instar larvae showed the highest values for all the dependent parameters (Quantity of
177
food ingested (mg), quantity of food digested (mg), efficiency of conversion of ingested food into
178
biomass (%), efficiency of conversion of digested food into biomass (%), corrected weight of
179
consumed leaves (mg), approximate digestibility (%), consumption index (mg), growth rate (mg)
180
and consumed leaf area (cm2)) followed by fourth and third instar larvae of S.litura (Fig 1-8).
181
Discussion
182
As the results showed that approximate digestibility for the fourth instar larvae of S. litura
183
fluctuates between 63.42-69.45%. First, it increases from 66.84%-69.45% and then decreases to
184
63.42%. These results are partially consistent with the findings of Rashwan (2013) who worked
185
on cotton leafworm S. littoralis and observed a decrease in approximate digestibility (control) with
186
an increase in larval age. This small difference may be due to the change of species or in the
187
composition of food as they were reared on leaves of castor bean. Evans (1939) reported that the
188
reasons for a decrease in approximate digestibility could be described as the insects are small
189
individuals which cut off tiny parts of food and give a large surface for the process of digestion,
190
and as they grow older, the nature of the food chosen by them also varies. The results of the present
191
study indicated that efficiency to convert the ingested food into biomass (40.65%-52.42%) and
192
capability to convert the digested food into biomass (39.77%-53.95%) values increased with an
193
increase in time.
194
In fifth instar larvae of S. litura the ingestion, digestion, consumption index and growth rate
195
increases from 12.60-19.40 mg, 11.93-15.28 mg, 2.42-2.56 %, and 0.71-0.89%, respectively.
196
These outcomes are in agreement with the findings of Rath (2010) who worked on nutritional
197
parameters of Antheraea mylitta larvae by offering them fresh leaves of Tilia tomentosa. 7
198
Nutritional indices like the relative consumption rate, ingestion, relative growth rate, digestion,
199
and gain in body weight increased significantly with an increase in the number of diets per day,
200
but approximate digestibility and efficiency in converting the ingested food into biomass declined,
201
while ability in converting the digested food into biomass did not change.
202
Approximate digestibility of third (51.36%-64.03%), fourth (63.42%-69.45%) and fifth (70.25%-
203
76.10%) instar larvae first increased and then decreased, while conversion efficiency of ingested
204
food into bio-mass varies significantly between 33.85-41.59%, 40.65-52.42%, 51.21-60.28% for
205
third, fourth and fifth instar of armyworm, respectively. However, efficiency conversion of
206
digested food into bio-mass values rose between ranges of 34.26-41.84%, 39.77-53.95%, 45.23-
207
61.75% for third, fourth and fifth instar of S. litura, correspondingly. These results are in line with
208
the research outcome of Kumar and Ballal (1992) who determined the impact of parasitization by
209
Hyposoter didymator on food utilization of S. litura and found that feeding potential, faeces
210
produced and weight gained were significantly less and AD was higher in infected larvae, while
211
ECI and ECD was highest in unparasitized larvae of armyworm. The outcome mentioned above
212
of present research is also consistent with the results of Reynolds et al. (1985), who found that
213
approximate digestibility was about 60% while EC1 and ECD were both very high. EC1 was 43%
214
and ECD was 72% in fifth instar larvae of Manduca sexta (Lepidoptera: Sphingidae). However,
215
the results were found in controversy with the findings of Teimouri et al. (2015) who determined
216
the relative consumption rate to be 5.36, 11.10 and 10.631 (mg/mg/day) on artificial diet, Akbari
217
and Kalequchi cultivars, respectively. While, according to our results, its values are between 0.84-
218
0.87 mg, 1.14-1.99 mg and 2.42-2.56 mg for third, fourth and fifth larval instars of S. litura,
219
correspondingly. Carob moth Ectomyelois ceratoniae (Zeller) (Lepidoptera: Pyralidae) larvae
220
reared on Akbari cultivar showed the highest ECD (5.64 ± 0.43). The highest amount of ECI was
221
obtained on artificial diet, but approximate digestibility (AD) was the lowest on this diet. These
222
differences may be due to the difference between two species of insects as they have different size,
223
and their metabolism is also different from each other. It might be due to the difference in the
224
composition, nature and type of food used by Teimouri et al. (2015).
225
These results are partially similar to the findings of Rath (2010) who found that dry matter
226
ingested, digested, ECD and biomass gain increased with the increase of larval development of A.
227
mylitta. A similar trend was observed in S. litura, where ingestion (10.01-19.40 mg/72 h), digestion 8
228
(8.32-15.28 mg/72 h) and ECD (34.26%-61.75%) increased with the increase of larval
229
development. While the relative consumption rate and growth rate was declined, and this trend
230
was observed only in the fourth instar larvae of S. litura. This might be due to the difference in
231
size as the larger insects consume less energy for their growth as compared to the smaller insects,
232
despite high growth rate (Reynolds et al., 1985; Rath et al., 2003).
233
Hemati el al. (2012) checked the effect of different plant species on nutritional indices of H.
234
armigera. It was found that third larval instar developed on potato indicated the highest amount of
235
ECD and ECI (50.80 ± 0.11% and 13.63 ± 0.02%, respectively), and the same trend of ECD and
236
ECI (41.84 ± 0.06% and 41.59 ± 0.06%, respectively) was observed in the current study. They
237
reported that AD of the fourth instar larvae was highest (92.65%) on chickpea (Azad) and least
238
(57.14%) on potato (Agria). Likewise, we also found maximum and minimum AD value (69.45 ±
239
0.09 % and 63.42 ± 0.07%, respectively) for the fourth instar of S. litura. They reported that fifth
240
larval instar reared on tomato and white kidney bean showed the great amount of feeding (3.71
241
mg) and relative consumption rate (1.62 mg), respectively. However, the result of present study
242
indicated that consumption index and growth rate values of fifth larval instar of S. litura were 2.56
243
± 0.03 mg and 0.89 ± 0.03 mg, respectively.
244
Maximum leaf area was consumed by fifth instar larvae of armyworm (44.66 cm2) followed by
245
fourth (35.41 cm2) and third (27.98 cm2) instar larvae. The findings of the present work are
246
consistent with the results of Dhir et al. (1992) who determined the losses in groundnut caused by
247
the tobacco caterpillar, S. litura and found that one larva/plant consumed about 54.7% of leaf area.
248
At flowering and pegging stage, single larva per plant consumed the 49.1% and 38.8% of leaf area
249
and reduced the yield upto19% and 5.7%, respectively.
250
Conclusion
251
It was concluded that maximum feeding potential (leaf-area/weight/mass consumed per larvae),
252
food utilization and consumption indices (consumption index, conversion efficiency of ingested
253
food into bio-mass, corrected weight of consumed leaves, growth rate, conversion efficiency of
254
digested food into bio-mass, consumed area of leaf, approximate digestibility, quantity of food
255
ingested and quantity of digested diet) and losses promises (% dry-weight and wet-weight loss)
256
were observed in T3 (fifth larval instar) followed by T2 (fourth larval instar) and T1 (third larval 9
257
instar). This is due to the fifth instar larvae were larger, their body metabolism was fast that is why
258
they consumed more food. Ultimately, digestion was also significant, efficiency to covert the
259
quantity of food digested into bio-mass, consumption, growth rate and capability to covert the
260
quantity of food ingested into bio-mass values were also higher. So, by managing this pest we can
261
reduce the losses as this pest can cause 25.8%-100% losses in different crops, especially in
262
vegetables.
263
Conflict of Interest
264
All authors declare no conflict of interests
265
Acknowledgements
266
We are profoundly grateful to Higher Education Commission (HEC) Pakistan who provided the
267
financial support to this project. We also acknowledge the support of the King Khalid University
268
(RCAMS/KKU/010-19) Research Center for Advanced Materials Science (RCAMS) at King
269
Khalid University, Kingdom of Saudi Arabia.
270
References
271
Ali, H., Qasim, M., Saqib, H.S.A., Arif, M., Islam, S.U., 2015. Synergetic effects of various plant
272
extracts as bio-pesticide against Wheat Aphid (Diurophous noxia L.)(Hemiptera:
273
Aphididae). Afric. J. Agric. Sci. Technol. 3(7): 310-315.
274 275
Ali, H., Hou, Y., Tang, B., Shi, Z., Muhammad, A., Sanda, N.B., 2016. A way of reproductive manipulation and biology of Wolbachia pipientis. J. Exp. Biol. Agric. Sci., 4(2) 156-168.
276
Ali, H., Muhammad, A., Bala, N.S., Wang, G., Chen, Z., Peng. Z., Hou, Y., 2018a. Genomic
277
evaluations of Wolbachia and mtDNA in the population of coconut hispine beetle,
278
Brontispa longissima (Coleoptera: Chrysomelidae). Mol. Phylogenet. Evol. 127:1000-
279
1009.
280
Ali, H., Muhammad, A., Bala, N.S., Hou, Y., 2018b. The endosymbiotic Wolbachia and host COI
281
gene enable to distinguish between two invasive palm pests; coconut leaf beetle, Brontispa
282
longissima and hispid leaf beetle, Octodonta nipae. J. Econ. Entomol. 111 (6): 2894–290. 10
283
Ali, H., Muhammad, A., Islam, W., Hou, Y., 2018c. A novel bacterial symbiont association in the
284
hispid beetle, Octodonta nipae (Coleoptera: Chrysomelidae), their dynamics and
285
phylogeny. Microb. Pathog. 118:378-386.
286
Ali, H., Muhammad, A., Hou, Y., 2018d. Infection density dynamics and phylogeny of Wolbachia
287
associated with coconut hispine beetle, Brontispa longissima (Gestro) (Coleoptera:
288
Chrysomelidae) by multilocus sequence type (MLST) genotyping. J. Microbiol. Biotechn.
289
28(5):796-808.
290
Ali, H., Muhammad, A., Hou, Y., 2018e. Absence of Wolbachia in Red Palm weevil,
291
Rynchophorus ferrugineus Olivier (Coleoptera: Curculionidae): A PCR based approaches.
292
Appl. Ecol. Env. Res. 16(2):1819-1833.
293
Arif, M., Islam, S.U., Adnan, M., Anwar, M., Ali, H., Wu, Z., 2018. Recent progress on gene
294
silencing/suppression by virus-derived small interfering RNAs in rice viruses especially
295
Rice grassy stunt virus. Microb. Pathog. 125: 210-218.
296
Bala, N.S., Muhammad, A., Ali, H., Hou, Y., (2018). Entomopathogenic nematode Steinernema
297
carpocapsae surpasses the cellular immune responses of the hispid beetle, Octodonta nipae
298
(Coleoptera: Chrysomelidae). Microb. Pathog. 124: 337-345.
299 300 301 302 303 304
Ahmad, M., Ghaffar, A., Rafiq, M., 2013. Host plants of leafworm, Spodoptera litura (fabricius) (Lepidoptera: Noctuidae) in Pakistan. Asian J. Agri. Biol. 1(1): 23-28. Arapitsas, P., 2008. Identification and quantification of poly phenolic compounds from okra seeds and skins. Food Chem. 110: 1041-1045. Benchasri, S., 2012. Okra (Abelmoschus esculentus (L.) Moench) as a valuable vegetable of the world. Ratar. Povrt. 49: 105-112.
305
Benjawan, C., Chutichudet, P., Kaewsit, S., 2007. Effect of green manures on growth yield and
306
quality of green okra ( Abelmoschus esculentus L.) harlium cultivar. Pakistan J. Biol. Sci.
307
10: 1028-1035.
308 309
Chaudhary, H.R., Dadheeck, L.N., 1989. Incidence of insects attacking okra and the avoidable losses by them. Ann. Arid Zone. 28: 305-307.
310
Dhir, B.C., Mohapatra, H.K., Senapati, B., 1992. Assessment of crop loss in groundnut due to
311
tobacco caterpillar, Spodoptera litura (F.). Indian J. Plant Protect. 20(2): 215-217. 11
312
Dilruba, S., Hasanuzzaman, M., Karim, R., Nahar, K., 2009. Yield response of okra to different
313
sowing time and application of growth hormones. J. Hort. Sci. Ornamental Plants. 1: 10-
314
14.
315 316 317 318 319 320 321 322
Ek-Amnuay, P., 2010. Plant diseases and insect pests of economic crops. Amarin Printing and Publishing Public Co. Ltd, Bangkok, Thailand. Pp. 379. Evans, A.C., 1939. The utilization of food certain lepidopterous larvae Trans. R. Ent. Soc. London. 89: 13-22. FAOSTAT (Food and Agricultural Organization), 2008. (http://www.fao.org). Accessed on 4-112014. Fasunwon, B.T., Banjo, A.D., 2010. Seasonal population fluctuations of Podagrica Species on okra plant (Abelmoschus esculentus). Res. J. Agric. Biol. Sci. 6: 283-288.
323
Fajinmi, A.A., Fajinmi, O.B., 2010. Incidence of okra mosaic virus at different growth stages of
324
okra plants (Abelmoschus esculentus (L.) Moench) under tropical condition. J. General
325
Mol. Virol. 2: 28-31.
326 327
Ghanem, G.A.M., 2003. Okra leaf curl virus: a mono partite begomovirus infecting okra crop in Saudi Arabia. Arab J. Biotechnol. 6: 139-152.
328
Ghanema, H.A.E., 2002. Studies on the environmental toxicity of some insecticides among the
329
cotton leafworm Spodoptera littoralis (Boisd.) PhD Thesis, Plant Protection Department,
330
Faculty of Agrculture, Zagazig University. 1-194 pp.
331 332
Gopalan, C., Sastri, S.B.V. and Balasubramanian, S., 2007. Nutritive value of Indian foods, National Institute of Nutrition (NIN), ICMR, India. Pp. 1-156.
333
Hemati, S.A., Naseri, B., Ganbalani, G.N., Dastjerdi, H.R. and Golizadeh, A., 2012. Effect of
334
different host plants on nutritional indices of the pod borer, Helicoverpa armigera. J. Insect
335
Sci. 12 (55): 1-15.
336 337
Hill, D., 1975. Spodoptera litura(F.) In: Agricultural Insect Pests of the Tropics and their control, Hill, D., (Eds.). Cambridge University Press, London, UK. Pp. 499.
338
Kahlon, T.S., Chapman, M.H., Smith, G.E., 2007. In vitro binding of bile acids by okra, beets,
339
asparagus, eggplant, turnips, green beans, carrots and cauliflower. Food Chem. 103: 676-
340
680.
12
341
Kaleri, A.W., Lohar, M.K., Marri, J.M., Nahiyoon, A.A., 2011. Role of trap crops in control of
342
jassidAamrascabiguttulabiguttula) on okra crop at Tando Jam, Sindh-Pakistan. Pak. J.
343
Entomol. Karachi. 26 (2): 101-105.
344
Kumar, P., Ballal, C.R., 1992. The effect of parasitism by Hyposoter didymator (Hym.:
345
Ichneumonidae) on food consumption and utilization by Spodoptera litura (Lep.:
346
Noctuidae). Entomophaga. 37(2): 197-203.
347
Kumar, S., Dagnoko, S., Haougui, A., Ratnadass, A., Pasternak, D., Kouame, C., 2010. Okra
348
(Abelmoschus spp.) in West and Central Africa: potential and progress on its improvement.
349
Afri. J.Agric. Res. 5: 3590-3598.
350
Lamont, W., 1999. Okra a versatile vegetable crop. Hort. Technol. 9: 179-184.
351
N’guessan, K.P., Fargette, D., Fauquet, C., Touvenel, J.C., 1992. Aspects of the epidemiology of
352 353 354 355 356
okra leaf curl virus in CôtedIvoire. Tropical Pest Manag. 38: 122-126. Nonnecke, I. L., 1989. Vegetable production AVI Book. Published by Van Nostrad. Reinhold, pp. 1-612. Owolarafe, O.K. and Shotonde, H.O., 2004. Some physical properties of fresh okra fruit. J. Food Engin. 63: 299-302.
357
Pal, S., Maji, T.B., Mondal, P., 2013. Incidence of insect pest on okra, Abelmoschus esculentus
358
(L) Moench in red lateritic zone of West Bengal. J. Plant Protect. Sci. 5(1): 59-64.
359
Purseglove, J. W., 1987. Tropical crop: dicotyedons. Language Book Society Longman, London,
360
UK. Pp. 1-719.
361
Qasim, M., Yongwen, L., Dash, C.K., Bamisile, B.S., Ravindran, K., Islam, S.I., Ali, H., Wang,
362
F., Wang, L., 2018. Temperature-dependent development of Asian citrus psyllid on various
363
hosts, and mortality by two strains of Isaria. Microb. Pathog. 119: 109-118.
364
Qasim, M., Husain, D., Islam, S.I., Ali, H., Islam, W., Hussain, M., Wang, F., Wang, L., 2018.
365
Effectiveness of Trichogramma chilonis Ishii against spiny bollworm in Okra and
366
susceptibility to insecticides. J. Entomol. Zool. Stud. 2018; 6: 1576-1581.
367 368 369 370
Qureshi, Z., 2007. Breeding investigation in bhendi (Abelmoschus esculentus (L.) Moench). Master Thesis, University of Agriculture Sciences, GKVK, Bangalore. Pp. 1-73. Rao, G., Wightman, J., Rao, D.R., 1993. World review of the natural enemies and diseases of Spodoptera litura (F.) (Lepidoptera: Noctuidae). Insect Sci. Appl. 14: 273-284.
13
371
Rashwan, M.H., 2013. Impact of Certain Novel Insecticides on Food Utilization Ingestion and
372
Larval Growth of the Cotton Leafworm Spodoptera littoralis (Boisd.). New York Sci. J.
373
6(8): 1-7.
374
Rath, S.S., Prasad, B.C., Sinha, B.R.R.P., 2003. Food utilization efficiency in fifth instar larvae of
375
Antheraea (Lepidoptera: Saturniidae) infected with Nosema sp. and its effect on
376
reproductive potential and silk production. J. Invert. Pathol. 83: 1-9.
377 378 379 380
Rath, S.S., 2010. Impact of Quantitative Feeding on Nutritional Parameters of Fifth Instar Larvae of Antheraea mylitta. Int. J. Indust. Entomol. 20(2): 69-74. Rath, S.S., 2010. Food utilization efficiency in Antheraea mylitta fed on Terminalia arjuna leaves. Acad. J. Entomol. 3(1): 23-28.
381
Reynolds, S. R., Nottingham, S. F., Stephens, A. E., 1985. Food and water economy and its relation
382
to growth in fifth-instar larvae of the tobacco hornworm, Manduca sexta. J. Insect. Physiol.
383
31(2): 119-127.
384 385
Saifullah, M., Rabbani, M.G., 2009. Evaluation and characterization of okra ( Abelmoschus esculentusL. Moench.) genotypes. SAARC J. Agric. 7: 92-99.
386
Shakeel, M., Ali, H., Ahmad, S., Said, F., Khan, K.A., Bashir, M.A., Anjum, S.I., Islam, W.,
387
Ghramh, H.A., Ansari, M.J., Ali, H., 2018. Insect pollinators diversity and abundance in
388
Eruca sativa Mill. (Arugula) and Brassica rapa L. (Field mustard) crops. Saudi J. Biol. Sci.
389
(in press).
390 391
Sridevi, A., 2009. Determination and comparison of nutritional indices in commercial silkworm hybrids during various instars. Asian J. Anim. Veterin. Adv. 4(3): 104-113.
392
Teimouri, N., Sendi, J. J., Zibaee, A., Khosravi, R., 2015. Feeding indices and enzymatic activities
393
of carobmoth Ectomyelois ceratoniae (Zeller) (Lepidoptera: pyrallidae) on two
394
commercial pistachio cultivarsand an artificial diet. J. Saudi Soci. Agri. Sci. 14: 76-82.
395
Varmudy, V., 2011. Marking survey need to boost okra exports. Department of economics,
396 397 398
Vivekananda College, Puttur, Kar-nataka, India. Pp. 21-23. Waldbauer, G.P., 1968. The consumption and utilization of food by insects. Adv. Insect Physiol., 5: 229-288.
399
Waterhouse, D., Norris, K., 1987. Spodoptera litura (Fabricius). In: Biological Control: Pacific
400
Prospects. Waterhouse D.F. and K. Norris, (Eds.). Australian Centre for International
401
Agricultural Research, Canberra. Pp. 250-259. 14
402
Zhou, Z., Chen, Z., Xu, Z., 2010. Potential of trap crops for integrated management of the tropical armyworm, Spodoptera litura in tobacco. J. Insect Sci. 10: Pp. 117.
403 404
Conflict of Interest
405
All authors declare no conflict of interests
Dependent Parameters
Quantity of food ingested (mg) Quantity of food digested (mg) Efficiency of conversion of ingested food to biomass (%) Efficiency of conversion of digested food to biomass (%) Corrected weight of consumed leaves (mg) Approximate Digestibility (%) Consumption index (mg) Growth rate (mg) Consumed leaf area (cm2)
DF
24h
48h
72h
F value
P value
F value
P value
F value
P value
2a/33b 2a/33b 2a/33b
12.8 12.3 20.7
0.01* 0.00* 0.00*
8.96 7.49 45.6
0.00* 0.03* 0.00*
1.00 1.30 1.68
0.03* 0.02* 0.02*
2a/33b
19.0
0.00*
44.1
0.00*
1.72
0.01*
2a/33b
3.25
0.03*
0.19
0.04*
5.34
0.00*
2a/33b 2a/33b 2a/33b 2a/33b
0.66 44.4 0.02 13.5
0.02* 0.00* 0.01* 0.00*
0.25 48.1 1.65 11.6
0.00* 0.00* 0.02* 0.00*
8.37 95.2 0.58 2.35
0.01* 0.00* 0.04* 0.01*
406 407 408
Highlights
409
The lepidopteran insect pests have significant importance in vegetable production
410
All dependent parameters and losses promises of leaf worm on Okra were evaluated
411
The consumption index values increased with an increase in time
412
All dependent parameters were higher for fifth instar larvae than others.
413
These results emphasized the re-establishment of fundamental IPM.
414 415 416 417 15
418
Table 1. Analysis of variance of data regarding quantity of food ingested (mg), quantity of food
419
digested (mg), efficiency of conversion of ingested food into biomass (%), efficiency of conversion
420
of digested food into biomass (%), corrected weight of consumed leaves (mg), approximate
421
digestibility (%), consumption index (mg), growth rate (mg) and consumed leaf area (cm2) by 3rd,
422
4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours (degree of
423
freedom of replication = 2) Treatments (3rd, 4th and 5th instars of Spodoptera litura).
424 425 426 3rd instar
Quantity of food ingested (mg)
25
4th instar
19.4 C
20 15
5th instar
17.28 A 12.98 AB 13.06 A
14.12 AB 11.27 B
10.01 B
15.29 B 12.6 A
10 5 0 24 hours
48 hours Feeding durations
72hours
427 428 429
Fig. 1. Quantity of food ingested (mg) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
430
16
3rd instar
4th instar
5th instar
Quantity of food digested (mg)
18 16 14 12 10
11.93A 10.96 B
12.94B 13.16 A 10.82C
14.03B
15.28A
11.91C
8.32 C
8 6 4 2 0 24 hours
48 hours Feeding Durations
431 432 433
72hours
Fig. 2. Quantity of food digested (mg) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
434
Efficiency of conversion of ingested food to biomass (%)
435 3rd instar
4th instar
5th instar
70
60.28A
60 50 40
51.21A 40.65B 33.85C
54.08A 45.84B 36.17C
52.42B 41.59C
30 20 10 0 24 hours
48 hours Feeding Durations
72hours
436 437 438
Fig. 3. Efficiency of conversion of ingested food to biomass (%) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
439 17
Efficiency of conversion of digested food to biomass (%)
3rd instar
4th instar
5th instar
70
60.78B 61.75A 53.95A
60 50 40
41.84A 36.29AB 34.26B
47.14B
41.59C
36.17C
30 20 10 0 24 hours
48 hours Feeding Durations
72hours
440 441 442
Fig. 4. Efficiency of conversion of digested food to biomass (%) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
443 444 445 446
Corrected weight of consumed leaves (mg)
447 3rd instar
4th instar
3.5
3.05A
3
2.72A
2.5 2
5th instar
1.83C
2.04B
2.98A 2.63AB
2.55AB 2.01B
1.91B
1.5 1 0.5 0 24 hours
48 hours Feeding durations
448
18
72hours
449 450
Fig. 5. Corrected weight of consumed leaves (mg) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
451 3rd instar
4th instar
Approximate digestibility (%)
90 80 70
70.25A 66.84AB 61.67B
69.45AB 64.03B
5th instar 76.1A
60
72.68A 63.42B 51.36C
50 40 30 20 10 0 24 hours
452 453 454
48 hours Feeding durations
72hours
Fig. 6. Approximate digestibility (%) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
455 456 457 458 459
19
3rd instar
4th instar
5th instar
Consumption index (mg)
3 2.5
2.56A
2.46A
2.42A 1.99B
2
1.98B
1.5
1.14B 0.87C
0.84C
1
0.85C
0.5 0 24 hours
48 hours Feeding durations
72hours
460 461 462 463
Fig. 7. Consumption index (mg) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
464 3rd instar
4th instar
5th instar
1
0.89A
0.9 Growth rate (mg)
0.8 0.7
0.69AB0.71A 0.61B
0.78B
0.76A 0.67AB 0.64B
0.67C
0.6 0.5 0.4 0.3 0.2 0.1 0 24 hours
465 466 467
48 hours Feeding Durations
72hours
Fig. 8. Growth rate (mg) by 3rd, 4th and 5th instar larvae of armyworm (Spodoptera litura) after 24, 48 and 72 hours of feeding
468 20