Biology and Bionomics of Dusky Cotton Bug (Oxycarenus laetus) (Lygaeidae: Hemiptera) on Three Different Hosts
Biology and Bionomics of Dusky Cotton Bug (Oxycarenus laetus) (Lygaeidae: Hemiptera) on Three Different Hosts
Muhammad Sarmad, Syed Muhammad Zaka* and
Syed Muhammad Tahir Abbas Shah
Department of Entomology, Faculty of Agricultural Sciences and Technology, Bahauddin Zakariya University, Multan, Pakistan.
ABSTRACT
The dusky cotton bug, Oxycarenus laetus Kirby. (Lygaidae: Hemiptera) had become a critical pest of cotton crop. Dusky cotton bug feeds on leaves, stems and seeds of host plants. Being a serious pest of many important crops, the present work will study on biology and bionomics of O. laetus on three different hosts Gossypium hirsutum, Abelmoschus esculentus and Helianthus annuus. Shorter nymphal duration was observed on Gossypium hirsutum 20.00 ±0.14 days as compared to Abelmoschus esculentus 21.00 ±0.26 days and Helianthus annuus 23.80 ±0.20 days. The longer adult life was observed on G. hirsutum (female 13.40 ±0.76 days and male 12.20 ±0.22 days) as compared to A. esculentus (female 9.40 ±0.40 days and male 8.20 ±0.37 days) and H. annuus (female 11.40 ±0.51 days and male 10.20 ±0.58 days). Fecundity (mean number of eggs) was significantly highestin case of G. hirsutum (16.33 ±0.88)as compared to A. esculentus (11.67 ±0.67) and H. annuus (6.67 ±0.33). Biology and bionomic study on different hosts will help the researchers make IPM strategies.
Article Information
Received 30 March 2019
Revised 11 July 2019
Accepted 11 September 2019
Available online 01 May 2020
Authors’ Contribution
MS performed the experiments. SMZ supervised the work. SMTAS coordinated the experiments.
Key words
Oxycarenus laetus, Bionomics, Gossypium hirsutum, Abelmoschus esculentus, Helianthus annuus
DOI: https://dx.doi.org/10.17582/journal.pjz/20190330090327
* Corresponding author: [email protected]
0030-9923/2020/0004-1619 $ 9.00/0
Copyright 2020 Zoological Society of Pakistan
Cotton is one of the main cash crops which account 5.1 percent in agriculture value addition and 1.0 percent of GDP in Pakistan. It provides raw material for textile industries and cotton lint is also exported. The crop was cultivated on 2917 thousand hectare during the year, 2015-16 (Anonymous, 2015-16). Average per acre yield of cotton is still low after many struggles in Pakistan as compared to other states (Bakhsh et al., 2005). Insect pests are the most significant factors that causing 30-40% yield loss of cotton (Kannan et al., 2004). In all cotton growing areas dusky cotton bug Oxycranus laetus (Hemiptera: Lygaeidae) is the most important pest that cause losses at economic level (Henry, 1983). Seeds of cotton appear undamaged but seed weight reduces up to 15% by internal feeding of O. laetus. Seeds are unable to grow and became useless. The damage of O. laetus also results in lint staining of cotton and seed quality deteriorate (Khan and Ahmed, 2000). O. laetus population also affects stored cotton (Henry, 1983). Severe attack of bugs results in less germination of seeds. It produces unpleasant smell when fed on cotton seeds. (Nakache, 1992; Thangavelu, 2007). O. laetus female prefers new bolls during oviposition (Sharma and Pamphapathy, 2006; Samy, 2007). Nymphs and adults of dusky cotton bug fed on stem, seeds and leaves of host plants (Sewify and Semeada, 1993). Feeding of dusky cotton bug was also reported on apple, maize, dates, figs, grapes, peach, okra and pineapple (USDA, 2009). Dusky cotton bug can feed on young petiole tissues (Holtz, 2006). Currently dusky cotton bug has 40 hosts reported from malvales order. These host plants produce seeds for dusky cotton bug at different time intervals of the year (Schaefer and Panizzi, 2000). Focus of our work was to explore the knowledge about comparative biology of O. laetus on three different hosts Gossypium hirsutum, Abelmoschus esculentus and Helianthus annuus and to study comparative change in bionomics on different hosts i.e. body length, width, antennal size, proboscis, pro-leg, meso-leg, meta-leg, fore and hind wing size of O. laetus.
Materials and methods
The adults of O. laetus were collected from cotton field of Bahauddin Zakariya University, Multan, Punjab, Pakistan on 2 October, 2017. The adults were reared in plastic jar (11×4×4 inches). The mouth of jars were covered with the muslin cloth and tied with the rubber band. Rearing was done under the laboratory condition 27 ±2°C, 70 ±5% R.H and photoperiod L14: D10 h. For rearing, cotton seeds (Gossypium hirsutum) were obtained from cotton research station Multan, while okra seeds (Abelmoschus esculentus) and sun flower seeds (Helianthus annuus) were obtained from local nursery. Soaked seeds were provided in separate petri dishes for feeding of O. laetus. Seeds were changed after every two days. Cotton soaked in water and placed in each jar to maintain the moisture level.
To study the reproductive biology of O. laetus on three hosts, fifteen newly hatched nymphs were selected from the collection and placed in petri dishes separately provided (Gossypium hirsutum, Abelmoschus esculentus and Helianthus annuus) seeds and very small cotton soak for moisture. Nymphal duration and adult longevity of both male and female of O. laetus were also recorded by observing either with eyes or where necessary with a simple microscope.
For studying bionomics, five replications were made and each replication representing five individuals of each instar which were randomly selected. Length and width of each body parts were measured. Stage micrometer (0.01-1 mm) ocular micrometer (0.2-2.5 mm) and graded scales (1-150 mm) were used for taking the measurement of each body part.
The data were statistically analyzed according to Completely Randomized Design on Statistical Analysis System (SAS Institute, 2002).
Results and discussion
First nymph: Duration of the first nymph was longer on H. annuus i.e. 4.40 ±0.24 days as compared to that of A. esculentus 4.00 ±0.32 days and G. hirsutum 3.80 ±0.22 days (P= 0.284, F= 1.40, df= 2, 14) (Fig. 1). The length of meso-leg was significantly greater on G. hirsutum 0.84 ±0.02 mm than that of H. annuus 0.76 ±0.04 mm and A. esculentus 0.74 ±0.02 mm (P= 0.041, F= 3.00, df= 2). Proboscis length 1.22 ±0.04 mm, antennal length 0.80 ±0.03 mm, length of pro-leg 0.62 ±0.04 mm, length of meta-leg 1.02 ±0.02 mm, body length 1.08 ±0.04 mm and body width 0.24 ±0.02 mm were found to be highest on G. hirsutum than other two hosts i.e. A. esculentus and H. annuus (Table I).
Second nymph: Duration of second nymph was longer on H. annuus i.e. 5.20 ±0.37 days as compared to A. esculentus 4.40 ±0.40 days and G. hirsutum 4.40 ±0.27 days (P= 0.210, F= 1.78, df= 2, 14) (Fig. 1). The body length of 2nd nymph was significantly greater on G. hirsutum 1.48 ±0.02 mm as compared to H. annuus 1.34 ±0.02 mm and A. esculentus 1.24 ±0.04 mm (P<0.0001, F= 16.67, df= 2). Measured length of proboscis 1.16 ±0.04 mm, length of antennae 0.94 ±0.02 mm, length of pro-leg 0.76 ±0.02 mm, length of meso-leg 0.96 ±0.02 mm, length of meta-leg 1.18 ±0.02 mm, and body width 0.38 ±0.02 mm were highest on G. hirsutum than other two hosts i.e. A. esculentus and H. annuus (Table I).
Third nymph: Duration of third nymph was longer on A. esculentus 5.00 ±0.45 days than other two hosts i.e. G. hirsutum and H. annuus (P= 0.291, F= 1.37. df= 2, 14) (Fig. 1). The size of pro-leg was same on G. hirsutum and A. esculentus 1.02 ±0.04 mm respectively and greater than H. annuus 0.94 ±0.04 mm. The length of meso-leg was significantly highest on G. hirsutum 1.24 ±0.02 mm as compared to H. annuus 1.16 ±0.02 mm and A. esculentus 1.14 ±0.02 mm (P= 0.031, F= 4.67, df= 2). Proboscis length 1.60 ±0.04 mm, antennal length 1.10 ±0.03 mm, length of meta-leg 1.46 ±0.02 mm, length of body 1.86 ±0.04 mm and length of width 0.78 ±0.04 were highest on G. hirsutum then A. esculentus and H. annuus (Table I).
Fourth nymph: Highest duration of fourth nymph 4.20 ±0.20 days was found on H. annuus than G. hirsutum 4.00 ±0.50 days and A. esculentus 3.40 ±0.51 days (P= 0.383, F= 1.04, df= 2, 14) (Fig. 1). Measured proboscis length 1.88 ±0.04 mm, antennal length 1.54 ±0.04 mm, length of pro-leg 1.36 ±0.02 mm, length of meso-leg 1.60 ±03 mm, length of meta-leg 1.94 ±0.05 mm and length of body 2.96 ±0.05 were greater on G. hirsutum than that of A. esculentus and H. annuus. The body width 1.16 ±0.02 mm was significantly higher on G. hirsutum than H. annuus and A. esculentus (P= 0.019, F= 5.56, df= 2) (Table I).
Fifth nymph: Duration of fifth nymph was significantly highest on H. annuus 5.20 ±0.20 days as compared to G. hirsutum 3.60 ±0.45 days and A. esculentus 4.20 ±0.49 days (P= 0.035, F= 4.45, df= 2, 14) (Fig. 1). The length of antennae 1.84 ±0.02 mm, length of meta-leg 2.32 ±0.04 mm, body length 3.58 ±0.04 mm and body width were significantly highest on G. hirsutum. Proboscis length 2.48 ±0.05 mm, length of pro-leg 1.56 ±0.02 mm and length of meso-leg 1.88 ±0.04 mm were found to be highest on G. hirsutum as compared to A. esculentus and H. annuus (Table I).
Table I. Bionomics of Oxycarenus laetus in relation to different stages.
Ins-ectsta-ges |
Seeds |
Size of different body parts (mm ± S.E) |
||||||||
Prob-oscis |
Ante-nnae |
Pro-leg |
Meso-leg |
Meta-leg |
Body length |
Body width |
Fore wing |
Hind wing |
||
1st instar |
G. hirsutum |
1.22 ±0.04a |
0.80 ±0.03a |
0.62 ±0.04a |
0.84 ±0.02a |
1.02 ±0.02a |
1.08 ±0.04a |
0.24 ±0.02a |
||
A. esculentus |
1.08 ±0.04a |
0.78 ±0.04a |
0.60 ±0.03a |
0.74 ±0.02b |
0.98 ±0.02a |
1.02 ±0.02a |
0.22 ±0.02a |
|||
H. annuus |
1.12 ±0.04a |
0.70 ±0.03a |
0.54 ±0.05a |
0.76 ±0.04ab |
0.96 ±0.04a |
1.04 ±0.02a |
0.18 ±0.04a |
|||
2nd instar |
G. hirsutum |
1.16 ±0.04a |
0.94 ±0.02a |
0.76 ±0.02a |
0.96 ±0.02a |
1.18 ±0.02a |
1.48 ±0.02a |
0.38 ±0.02a |
||
A. esculentus |
1.10 ±0.04a |
0.92 ±0.04a |
0.68 ±0.04a |
0.90 ±0.03a |
1.10 ±0.03a |
1.24 ±0.04c |
0.30 ±0.03b |
|||
H. annuus |
1.10 ±0.04a |
0.90 ±0.03a |
0.70 ±0.05a |
0.88 ±0.04a |
1.10 ±0.03a |
1.34 ±0.02b |
0.34 ±0.02ab |
|||
3rd instar |
G. hirsutum |
1.60 ±0.04a |
1.10 ±0.03a |
1.02 ±0.04a |
1.24 ±0.02a |
1.46 ±0.02a |
1.86 ±0.04a |
0.78 ±0.04a |
||
A. esculentus |
1.56 ±0.02a |
1.04 ±0.02a |
1.02 ±0.04a |
1.14 ±0.02b |
1.36 ±0.04a |
1.84 ±0.02a |
0.72 ±0.04a |
|||
H. annuus |
1.52 ±0.04a |
1.02 ±0.04a |
0.94 ±0.04a |
1.16 ±0.02b |
1.38 ±0.04a |
1.76 ±0.06a |
0.74 ±0.02a |
|||
4th instar |
G. hirsutum |
1.88 ±0.04a |
1.54 ±0.04a |
1.36 ±0.02a |
1.60 ±0.03a |
1.94 ±0.05a |
2.96 ±0.05a |
1.16 ±0.02a |
||
A. esculentus |
1.86 ±0.02a |
1.42 ±0.04a |
1.30 ±0.03a |
1.58 ±0.04a |
1.86 ±0.02a |
2.66 ±0.05b |
1.06 ±0.02b |
|||
H. annuus |
1.84 ±0.04a |
1.46 ±0.05a |
1.30 ±0.03a |
1.52 ±0.04a |
1.86 ±0.05a |
2.86 ±0.05a |
1.06 ±0.02b |
|||
5th instar |
G. hirsutum |
2.48 ±0.05a |
1.84 ±0.02a |
1.56 ±0.02a |
1.88 ±0.04a |
2.32 ±0.04a |
3.58 ±0.04a |
1.46 ±0.02a |
||
A. esculentus |
2.34 ±0.04a |
1.76 ±0.02b |
1.50 ±0.03a |
1.78 ±0.02a |
2.08 ±0.04b |
3.06 ±0.05b |
1.28 ±0.02b |
|||
H. annuus |
2.40 ±0.05a |
1.74 ±0.02b |
1.50 ±0.03a |
1.78 ±0.04a |
2.30 ±0.03a |
3.52 ±0.04a |
1.38 ±0.04a |
|||
Male adult |
G. hirsutum |
2.60 ±0.03a |
2.16 ±0.04a |
2.00 ±0.04a |
2.24 ±0.05a |
2.82 ±0.04a |
4.38 ±0.04a |
1.38 ±0.04a |
2.98 ±0.04a |
2.46 ±0.05a |
A. esculentus |
2.50 ±0.04a |
2.10 ±0.03a |
1.88 ±0.02b |
2.16 ±0.02ab |
2.56 ±0.02b |
3.92 ±0.04c |
1.28 ±0.02a |
2.82 ±0.04b |
2.44 ±0.02a |
|
H. annuus |
2.52 ±0.04a |
2.08 ±0.04a |
1.86 ±0.04b |
2.10 ±0.04b |
2.54 ±0.02b |
4.08 ±0.04b |
1.28 ±0.04a |
2.96 ±0.02a |
2.42 ±0.04a |
|
Fem-ale adult |
G. hirsutum |
2.78 ±0.04a |
2.36 ±0.04a |
2.16 ±0.04a |
2.48 ±0.04a |
3.06 ±0.02a |
4.68 ±0.04a |
1.60 ±0.03a |
3.10 ±0.03a |
2.56 ±0.04a |
A. esculentus |
2.72 ±0.02ab |
2.34 ±0.02a |
2.10 ±0.03a |
2.42 ±0.04ab |
2.96 ±0.02b |
4.52 ±0.04b |
1.52 ±0.04a |
3.04 ±0.02a |
2.42 ±0.04b |
|
H. annuus |
2.66 ±0.02b |
2.28 ±0.04a |
2.08 ±0.04a |
2.32 ±0.04b |
3.06 ±0.04a |
4.48 ±0.04b |
1.52 ±0.02a |
3.04 ±0.02a |
2.52 ±0.02ab |
Means followed by the same latters along the column are statistically non-significant (P<0.05). Analysis of all the stages was done separately.
Adult male: Significant highest duration of adult male 12.20 ±0.22 days was found on G. hirsutum than that of H. annuus 10.20 ±0.58 days and A. esculentus 8.20 ±0.37 days (P< 0.0001, F= 23.08, df= 2, 14) (Fig. 1). The length of pro-leg 2.00 ±0.04 mm, length of meso-leg 2.24 ±0.05 mm, length of meta-leg 2.82 ±0.04 mm, body length 4.38 ±0.04 mm and length of fore-wing 2.98 ±0.04 mm were significantly highest on G. hirsutum than A. esculentus and H. annuus. Measured proboscis length 2.60 ±0.03 mm, antennal length 2.16 ±0.04 mm, body width 1.38 ±0.04 mm and length of hind-wing 2.46 ±0.05 mm were higher on G. hirsutum as compared to A. esculentus and H. annuus (Table I).
Adult female: Duration of adult female 13.40 ±0.76 days was significantly higher on G. hirsutum as compared to H. annuus 11.40 ±.51 days and A. esculentus 9.40 ±0.40 days (P< 0.0001, F= 13.64, df=2, 14) (Fig. 1). The length of proboscis 2.78 ±0.04 mm, length of meso-leg 2.48 ±0.04 mm, length of meta-leg 3.06 ±0.02 mm, body length 4.68 ±0.04 mm and length of hind-wing 2.56 ±0.04 mm were significantly highest on G. hirsutum as compared to A. esculentus and H. annuus. Length of antennae 2.36 ±0.04 mm, length of pro-leg 2.16 ±0.04 mm, body width 1.60 ±0.03 mm and length of fore-wing 3.10 ±0.03 mm were greater than A. esculentus and H. annuus (Table I). The body length, width, antenna size, proboscis, foreleg, hind leg, fore-wing and hind-wing explain the vigor of insects on the hosts (Bilgrami and Gaugler, 2004). No previous studies have been found on the bionomics of O. laetus. In our study, we measured the body parts of both immature and mature stages of O. laetus. D. koenigii was reared on seeds of G. hirsutum and A. esculentus to keep up uniformity (Kohno and Ngan, 2004). Duration of nymphs was minimum on G. hirsutum. While, fecundity was maximum on G. hirsutum (Saxena, 1969).
Fecundity: Fecundity of O. laetus was significantly highest, when fed on G. hirsutum 16.33 ±0.88 eggs as compared to A. esculentus 11.67 ±0.67 eggs and H. annuus 6.67 ±0.33 eggs (P<0.0002, F= 52.58, df= 2) (Fig. 2). The highest survival and reproductive rate of insects have variation when fed on different hosts (Kumar and Sahu, 2009).
Conclusion
The study concludes that G. hirsutum is the most preferable host for survival, longevity and fecundity of O. laetus as compared to A. esculentus and H. annuus. A. esculentus and H. annuus do not grow in G. hirsutum growing areas but O. laetus can successfully complete their life cycle on these hosts. This study provides the frame work for future detailed study on the immature and mature stages of O. laetus.
Acknowledgement
The authors wish to acknowledge the Department of Entomology, Central Cotton Research Institute for coordinating in the present research work and undergraduate students for helping in experiments.
Statement of conflict of interest
The authors declare there is no conflict of interest.
References
Anonymous, 2015-16. Economic survey of Pakistan, Ministry of Finance, Government of Pakistan. http://www.finance.gov.pk
Bakhsh, K., Hassan, I. and Maqbool, A., 2005. J. Agric. Soc. Sci., 1: 332-334.
Bilgrami, A.L. and Gaugler, R., 2004. Feeding behaviour. Nematode behaviour (eds. R. Gaugler and A.L. Bilgrami). CABI, Wallingford,UK. pp. 91-126. https://doi.org/10.1079/9780851998183.0091
Henry, T., 1983. Pests not known to occur in the United States or of limited distribution, no. 38 cotton seed bug. United States Department of Agriculture, Animal and Plant Health Inspection Service. Plant Protection and Quarantine.
Holtz, T. 2006. Qualitative analysis of potential consequences associated with the introduction of the cotton seed bug (Oxycarenus hyalinipennis) into the United States. Available online at http://www.Monsanto.co.uk/news/ ukshowlib.html?wid=8478.
Kannan, M., Uthamasamy, S. and Mohan, S., 2004. Curr. Sci., 86: 726-729.
Khan, M. and Ahmed, S., 2000. Acta Biol. Cracov. Zool., 42: 372-376.
Kohno, K. and Ngan, B.T., 2004. Appl. Ent. Zool., 39: 183-187. https://doi.org/10.1303/aez.2004.183
Kumar, G. and Sahu, J., 2009. Eur. J. Ent., 106: 565-569. https://doi.org/10.14411/eje.2009.071
Nakache, Y. and Klein, M., 1992. The cotton seed bug attacked various crops in Israel in 1991.
Samy, O., 2007. J. Nat. Hist., 5: 367-384. https://doi.org/10.1080/00222937100770281
SAS Institute, 2002. The SAS system for Windows, Release 9.0, SAS Institute, Cary, N.C.
Saxena, K.N., 1969. Ent.. Exp. Appl., 12: 751-766. https://doi.org/10.1111/j.1570-7458.1969.tb02569.x
Schaefer, C.W. and Panizzi, A.R., 2000. Heteroptera of economic importance. CRC press. https://doi.org/10.1201/9781420041859
Sewify, G. and Semeada, A., 1993. Bull. Facul. Agric. Univ. Cairo, 44: 445-452.
Sharma, H.C. and Pampapathy, G., 2006. Crop Prot., 25: 800-813. https://doi.org/10.1016/j.cropro.2005.11.002
Thangavelu, K., 2007. J. Nat. His., 12: 289-294. https://doi.org/10.1080/00222937800770161
USDA. 2009. Significant pest bulletin: Cotton seed bug. United States Department of Agriculture.
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