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Shivalingaswamy, T. M.
- Mud Wasp, Sceliphron madraspatanum (Fabricius) (Hymenoptera: Sphecidae): A Threat or Nature's Regulation of Spider Fauna in the Vegetable Agroecosystem?
Authors
1 Crop Protection Division, Indian Institute of Vegetable Research, Varanasi 221 305, Uttar Pradesh, IN
2 National Bureau of Agriculturally Important Insects, Bangalore 560 024, IN
3 Division of Entomology, Indian Agricultural Research Institute, New Delhi 110 012, IN
Source
Journal of Biological Control, Vol 26, No 4 (2012), Pagination: 373–375Abstract
The biology and behaviour of mud wasp, Sceliphron madraspatanum (Fabricius) and its possible role in insect pest management were studied under vegetable agroecosystem. The gravid female lays a single egg (2.75±0.33 mm in length) in a mud chamber that is provisioned almost exclusively with orb-weaver spiders, wolf spiders and jumping spiders available in the vegetable agroecosystem. Total numbers of spiders provisioned in each cell was negatively correlated with their mean body weight. However, the wasps avoided provisioning of lynx spider, the most predominant spider in this ecosystem, due to its short and reduced abdomen and also the presence of large, strong and erect setae over its body. In the agroecosystem, mud wasp was found to constitute the third trophic level in the food chain comprising of the vegetable crops–insect pests–spiders–S. madraspatanum and thereby their role could be detrimental for the pest management.Keywords
Sceliphron madraspatanum, Biology, Prey Spiders, Tritrophic Interactions.References
- Elgar MA, Jebb M. 1999. Nest provisioning in the muddauber wasp Sceliphron laetum (F. Smith): Body mass and taxa specific prey selection. Behaviour 136: 147– 159.
- Freeman BE, Johnston B. 1978. The biology in Jamaica of the adults of the sphecid wasp Sceliphron assimile Dahlbom. Ecol Ent. 3(1): 39–52.
- Jackson RR, Brssington RJ. 1987. The biology of Pholcus phalangioides (Araneae, Pholcidae): predatory versatility, araneophagy and aggressive mimicry. J Zool. 211(2): 227–238.
- Kumari B, Kumar S. 2009. An insight into the ethnozoology of Panch Pargana area of Jharkhand, India. J Thr Taxa 1(8): 441–443.
- Landes DA, Martin S Obin, Cady, AB, Hunt JH. 1987. Seasonal and latitudinal variation in spider prey of the mud dauber Chalybion californicum (Hymenoptera: Sphecidae). J Arachn. 15(2): 249–256.
- Nyffeler M, Dean DA, Sterling WL. 1989. Prey selection and predatory importance of orb-weaving spiders (Araneae: Araneidae, Uloboridae). Texas Cotton Env Ent. 18(3): 373–380.
- Rajan V, Shukla AN. 1996. Towards ecological farming in India for poverty alleviation, environmental regeneration, and political stabilization. J Sust Agric. 6(4): 61–96.
- Sahu S, Singh R, Pawan K. 1996. Host preference and feeding potential of spiders predaceous on insect pests of rice. J Ent Res. 20(2): 145–150.
- Sunderland K. 1999. Spiders for pest control. Pesticide Outlook 4: 82–85.
- Okra Shoot and Fruit Borer, Earias vittella (F.), A New Host Record for the Egg Parasitoid, Trichogramma Chilotraeae Nagaraja and Nagarkatti from India
Authors
1 Indian Institute of Vegetable Research, Varanasi 221 305, Uttar Pradesh, IN
2 Central Research Institute for Jute and Allied Fibres, Barrackpore 700 120, West Bengal, IN
Source
Journal of Biological Control, Vol 25, No 2 (2011), Pagination: 146-147Abstract
An in situ survey on native natural enemies of okra shoot and fruit borer, Earias vittella was conducted during September-October 2008, at IIVR research farm, Varanasi, Uttar Pradesh, India. The survey revealed that Trichogramma chilotraeae Nagaraja and Nagarkatti is a potential egg parasitoid which was occurring naturally in the okra ecosystem in spite of the pubescence of the okra plant. This is the first record of natural parasitism of T. chilotraeae on E. vittella.Keywords
Earias vittella, Trichogramma chilotraeae, Okra, Record.- Variability in Foraging Behaviour, Thermal Requirement and Virulence of Entomopathogenic Nematodes against Sod Webworm, Herpetogramma phaeopteralis Guenee (Lepidoptera: Crambidae)
Authors
1 ICAR-National Bureau of Agricultural Insect Resources, P. B. No. 2491, H. A. Farm Post, Bellary Road, Hebbal, Bangalore − 560 024, Karnataka, IN
Source
Journal of Biological Control, Vol 33, No 1 (2019), Pagination: 36-47Abstract
Variability in virulence among entomopathogenic nematodes, Heterorhabditis indica, H. bacteriophora and Steinernema abbasi, was studied for lethality, foraging behaviour in response to host volatiles, thermal requirements (degree-days), recyclability, persistence and field efficacy against Turfgrass Sod Webworm (TSW), Herpetogramma phaeopteralis. Comparatively, lethal concentration and time were lowest for H. indica against TSW. Recyclability of EPN ranged from 3.42 × 105 to 4.23 × 105 IJs g1 of TSW. H. bacteriophora recorded highest movement rate on agar (0.38–0.78cm) and sand-agar (0.45–0.56cm), followed by S. abbasi, and H. indica. Responding to TSW volatiles, S. abbasi recorded maximum movement, H. bacteriophora, moderate, and H. indica, lowest. Heterorhabditis indica (with nictitation); S. abbasi and H. bacteriophora (without nictitation) were ambusher and cruiser, respectively. S. abbasi preferred warmer temperatures (30–33°C), H. bacteriophora, moderate (24–27°C), and H. indica, a wider range (24–30°C), for virulence based on thermal requirement. In field, EPNs were comparable to chlorpyriphos against TSW. We demonstrated the complementarity of thermal preferences of EPNs and insect pest was critical besides attributes like foraging behaviour, recyclability, persistence, and lethality values for their success in the field.Keywords
Degree-Days, Foraging, Herpetogramma phaeopteralis, Heterorhabditis indica, H. bacteriophora, Sod Webworm, Steinernema abbasi, Thermal Requirement, Turfgrass, Virulence, Variability.References
- Abbott WS. 1925. A method of computing the effectiveness of an insecticide. J Econ Entomol. 18: 265−267. https:// doi.org/10.1093/jee/18.2.265a.
- Bélair G, Koppenhöfer AM, Dionne J, Simard L. 2010. Current and potential use of pathogens in the management of turfgrass insects as affected by new pesticide regulations in North America. Intl J Pest Manage. 56: 51−60. https:// doi.org/10.1080/09670870903076012.
- Campbell JF, Gaugler R. 1993. Nictation behavior and its ecologicalimplications in the host search strategies of entomopathogenic nematodes (Heterorhabditidae and Steinernematidae). Behaviour 126: 155−169. https:// doi.org/10.1163/156853993X00092.
- Campbell JF, Gaugler R. 1997. Inter-specific variation in entomopathogenicnematode foraging strategy: dichotomy or variation along a continuum. Fundam Appl Nematol. 20: 393−398.
- Dhillon MK, Sharma HC. 2009. Temperature influences the performance and effectiveness of field and laboratory strains of the ichneumonid parasitoid, Campoletis chlorideae. BioControl 54: 743−750. https://doi.org/10.1007/s10526-009-9225-x.
- Ebssa L, Koppenhofer AM. 2011. Efficacy and persistence of entomopathogenic nematodes for black cutworm control in turfgrass. Biocontrol SciTechn. 21: 779−796. https://doi.org/10.1080/09583157.2011.584610.
- Glazer I, Lewis EE. 2000. Bioassays for entomopathogenic nematodes. pp. 229−247. In: Navon A, Ascher KRS (Eds.). Bioassays of Entomopathogenic Microbes and Nematodes. Wallingford, UK: CABI Publishing. https://doi.org/10.1079/9780851994222.0229.
- Grewal PS, Koppenhofer AM, Choo HY. 2005. Lawn, turfgrass, and pasture applications. Pp.115−146. In: Grewal PS, Ehlers RU, and Shapiro-Ilan DI, (Eds.). Nematodes as biocontrol agents. Wallingford: CABI Publishing. https://doi.org/10.1079/9780851990170.0115.
- Haydu JJ, Hodges AW, Hall CR. 2006. Economic impacts of the turfgrass and lawncare industry in the United States. University of Florida, IFAS, EDIS document FE 632.
- Hill MP, Malan AP, Terblanche JS. 2015. Divergent thermal specialisation of two South African entomopathogenic nematodes. Peer J. 3: e1023. http://doi.org/10.7717/peerj.1023. https://doi.org/10.7717/peerj.1023.
- Kaya HK. 1990. Soil ecology. Pp. 93−115. In: Gaugler R and Kaya HK, (Eds.). Entomopathogenic nematodes in biological control. Boca Raton: CRC Press.
- Klein MG, Grewal PS, Jackson TA, Koppenhofer AM. 2007. Lawn, turf and grassland pests.Pp. 655−675. In: Lacey LA and Kaya HK (Eds.), Field Manual of Techniques in Invertebrate Pathology: Application and evaluation of pathogens for control of insects and other invertebrate pests. Second Edition. Dordrecht: Springer. https://doi.org/10.1007/978-1-4020-5933-9_32.
- Koppenhofer AM, Grewal PS, Fuzy EM. 2006. Virulence of the entomopathogenic nematodes, Heterorhabditis bacteriophora, Heterorhabditis zealandica, and Steinernema scarabaei against five white grub species (Coleoptera: Scarabaeidae) of economic importance in turfgrass in North America. Biol Control 38: 397−404. https://doi.org/10.1016/j.biocontrol.2005.12.013.
- Kurtz B, Toepfer S, Ehlers RU, Kuhlmann U. 2007, Assessment of establishment and persistence of entomopathogenic nematodes for biological control of western corn ischolar_mainworm. J Appl Entomol. 131: 420−425. doi: 10.1111/j.1439-0418.2007.01202. https://doi.org/10.1111/j.1439-0418.2007.01202.x.
- Lacey AL, Georgis R. 2012. Entomopathogenic nematodes for control of insect pests above and below ground with comments on commercial production. J Nematol. 44(2): 218−225.
- Lewis EE. 2002. Behavioral Ecology. Pp. 205−224. In: Gaugler R, (Ed.), Entomopathogenic Nematology. Wallingford: CABI Publishing. https://doi.org/10.1079/9780851995670.0205.
- Lewis EE, Gaugler R, Harrison R. 1992. Entomopathogenic nematodehost finding: response to host contact cues by cruise and ambush foragers. Parasitology 105: 309−315. https://doi.org/10.1017/S0031182000074230.
- Lewis EE.Gaugler R, Harrison R. 1993. Response of cruiser and ambusher entomopathogenic nematodes (Steinernematidae) in host volatile cues. Can J Zool. 71: 765−769. https://doi.org/10.1139/z93-101.
- Meagher RL, Epsky ND, Cherry R. 2007. Mating behavior and female-produced pheromones use in tropical sod webworm (Lepidoptera: Crambidae). Fla Entomol. 90: 304−308. https://doi.org/10.1653/0015-4040(2007)90[304:MBAFPU]2.0.CO;2.
- Niemczyk HD. 1981. Destructive turf insects. HDN Book Sales. Wooster, OH. 48 pp.
- Noosidum A, Hodson AK, Lewis EE, Chandrapatya A. 2010. Characterization of new entomopathogenic nematodes from Thailand: foraging behavior and virulence to the Greater wax moth, Galleria mellonella L. (Lepidoptera: Pyralidae). J Nematol. 42: 281−291.
- Racke KD. 2000. Pesticide for turfgrass pest management uses and environmental issues. Pp-45. In: Clark M and M. P. Kennum MP (Eds.), Fate and Management of turf grass chemicals. https://doi.org/10.1021/bk-2000-0743.ch003.
- Reinert JA, Engelke MC, Genovesi AD, Chandra A, McCoy JE. 2009. Resistance to tropicalsod webworm (Herpetogramma phaeopteralis) (Lepidoptera:Crambidae) in St. Augustine grass and zoysia grass. Intl Turfgrass Society Res J. 11: 663−673.
- Shapiro-Ilan DI, Blackburn D, Duncan L, El-Borai FE, Koppenho¨fer H, Tailliez P, Adams BJ. 2014. Characterization of biocontrol traits in Heterorhabditis floridensis: A species with broad temperature tolerance. J Nematol. 46(4): 336−345.
- Tofangsazi N, Cherry RH, Arthurs SP. 2014. Efficacy of commercial formulations of entomopathogenic nematodes against tropical sod webworm, Herpetogramma phaeopteralis (Lepidoptera: Crambidae). J Appl Entomol. DOI: 10.1111/jen.12125. https://doi.org/10.1111/jen.12125.
- White GF. 1927. A method for obtaining infective nematode from cultures. Science 66: 302− 303. https://doi.org/10.1126/science.66.1709.302-a.
- Woodring LJ and Kaya KH. 1988. Steinernematid and Heterorhabditid nematodes. A handbook of biology and techniques. Southern Cooperative Series Bulletin. A publication ofthe nematode subcommittee of the Southern Research Project S135- Entomopathogens foruse in Pest Management Systems.
- Biodiversity of Pollinators in Four Bee-Friendly Plant Species
Authors
1 ICAR-National Bureau of Agricultural Insect Resources, Post Bag No. 2491, H. A. Farm Post, Hebbal, Bengaluru – 560024, Karnataka, IN
Source
Journal of Biological Control, Vol 33, No 4 (2019), Pagination: 360-364Abstract
Bees are the primary pollinators of many important agricultural crops. Enhancing the suitability of farm landscapes for native pollinators by growing flowering non crop plants is necessary for in-situ conservation of bee pollinators. A study has been conducted to find the role of four different plants, viz., Hamelia patens, Ocimum basilicum, Asystesia sp. and Jacquemontia sp. in the conservation of native bee pollinators. The different species of bees visiting the flowers were Apis cerana, A. florea, Hoplonomia sp., Amegilla zonata, A. confusa and Ceratina hieroglyphica. The diversity indices were higher during morning hours than the afternoon. The number of bees visited per flower, time spent and numbers of flowers visited on Jacquemontia sp. were more compared to other plant species. Biodiversity indices were calculated by using Insect Biodiversity Analysis Portal, which is an online tool to carry out biodiversity analysis and hosted at https://www.nbair.res.in/Biodiversity. The planting of bee-friendly plant species as identified in this study will help support healthy, diverse pollinator and other beneficial insect communities.Keywords
Bee Pollinators, Biodiversity Indices, In-Situ Conservation, Non-Crop Plants.References
- Duffy KJ, Johnson SD, Peter CI. 2014. A temporal dimension to the influence of pollen rewards on bee behaviour and fecundity in Aloe tenuior. PLoS ONE 9: e94908. https://doi.org/10.1371/journal.pone.0094908 PMid:24755611 PMCid:PMC 3995886
- Emile May. 2018. Managing land for pollinators and conservation biocontrol. https://www.ecolandscaping.org/01/landscaping-for-wildlife/beneficialspollinators/managing-land-pollinators-conservation-biocontrol/
- Fussell M, Corbet SA. 1992. Flower usage by bumblebees - a basis for forage plant management. J Appl Ecol. 29: 451-465. https://doi.org/10.2307/2404513
- Jones EL, Leather SR. Invertebrates in urban areas: A review. European J Entomol. 109: 463-478.
- Kremen C, Williams NM, Thorp RW. 2002. Crop pollination from native bees at risk from agricultural intensification. Proc Nat Acad Sci. 99: 16812-16816.https://doi.org/10.1073/pnas.262413599 PMid:12486221 PMCid: PMC139226
- Piedade-Kiill, Lucia H, Neusa Taroda R. 2000. Biologia floral e sistema de reprodução de Jacquemontia multiflora (Choisy) Hallier f. (Convolvulaceae). Rev Bras Fisioter. 23: 37-43. https://doi.org/10.1590/S0100-84042000000100004
- Pywell RF, Meek WR, Hulmes L, Hulmes S, James KL, Nowakowski M, Carvell C. 2011. Management to enhance pollen and nectar resources for bumble bees and butterflies within intensively farmed landscapes. J Insect Conserv. 15: 853-864. https://doi.org/10.1007/s10841-011-9383-x
- Silvia KD, Gimenes M. 2016. The efficiency of bees in pollinating ephemeral flowers of Jacquemontia bracteosa (Convolvulaceae). Iheringia Ser Zool. 106: ISSN 0073-4721, On-line version ISSN 1678-4766. https://doi.org/10.1590/1678-4766e2016025
- Biology and Potential of Pentatomid Predator, Eocanthecona furcellata (Wolff) (hemiptera: Pentatomidae) on Fall Armyworm, Spodoptera frugiperda (Smith)
Authors
1 Department of Entomology, UAS, Bengaluru – 560065, Karnataka, IN
2 Division of Germplasm Conservation and Utilization, ICAR-NBAIR, Hebbal, Bengaluru – 560024, Karnataka, IN
3 Resource Management in Plant Protection, ICAR-NBAIR, Hebbal, Bengaluru – 560024, Karnataka, IN
4 Department of Plant Pathology, UAS, Bengaluru – 560065, Karnataka, IN
5 Department of Crop Physiology, UAS, Bengaluru – 560065, Karnataka, IN
Source
Journal of Biological Control, Vol 34, No 1 (2020), Pagination: 26-29Abstract
Studies on the biology and feeding potential of Eocanthecona furcellata (Wolff) on Spodoptera frugiperda (Smith) were carried out at NBAIR, Bengaluru. Experimental results revealed that the total developmental period from egg to adult for male and female were 27.92±2.87 and 39.62±3.28 d, respectively. The life cycle of male and female passed through first, second, third, fourth and fifth nymphal instars (male: 2.42±0.51 d, 3.25±0.45 d, 3.25±0.45 d, 4.00±0.60 d, 4.42±0.51 d) and (female: 2.54±0.52 d, 3.46±0.52 d, 4.00±0.71 d, 4.38±0.65 d, 5.08±0.49 d), respectively. Total nymphal period is about 17.83±1.34 d for male and 19.46±1.20 days for female, respectively. Adult longevity of male is lower (10.25±2.96 d) compared to that of female (20.15±3.39 d). The premating period and mating period of adult E. furcellata was 2.33±0.50 days and 6.44±2.24 hrs, respectively. The pre-oviposition period, oviposition period of adult female was 2.89±0.60 and 11.22±1.72 days, respectively. The average number of eggs laid by the female was 209.29±28.11 in a single mated system. Egg incubation period was about 5.42±0.51 days. The predation rates of second, third, fourth, fifth instar nymphs, adult female and male on 2nd, 4th, 6th instar prey of E. furcellata were (16 ±0.95, 27 ±4.06, 55±4.67, 68 ±5.41, 126 ± 4.76, 97 ± 2.85), (7±1.34, 24±2.77, 40±3.39 45±0.71, 88±1.37, 51±1.60) and (4±0.82, 9±1.64, 21±2.81, 38±1.03, 69±1.32, 36±2.73), respectively.
Keywords
Biology, Developmental Period, Eocanthecona furcellata, Predatory Potential, Spodoptera frugiperda.References
- Ahmad M, Singh AP, Sharma S, Mishra RK and Ahmad MJ.1996. Potential estimation of predatory bug, Canthecona furcellata Wolff. against poplar defoliator, Clostera cupreata. Ann Forestry 4(2): 133–138.
- Basappa H. 2011. Biodiversity of biocontrol agents in sunflower ecosystem. J Biol Control 25(3): 182–187.
- Cherian MC and Brahmachari K. 1941. Notes on the three predatory hemipterans from south India. Indian J Entomol. 3: 115–119.
- Kumar S and Singh SV. 2007, Longevity fecundity and sex ratio of Canthecona furcellata on lepidopterous insect pests. Ann Plant Prot Sci. 15(7): 235–281.
- Lenin SEA and Rajan SJ. 2016. Biology of predatory bug Eocanthecona furcellata Wolff (Hemiptera: Pentatomidae) on Corcyra cephalonica. J Entomol Zool Stud. 4(3): 338–34.
- Nebapure SM and Agnihotri M. 2011. Canthecona furcellata: A predator of Maruca vitrata. Anna Plant Prot Sci. 19: 451–508.
- Pant CP. 1960. Some aspects of bionomics of Eariasw spp. at Kanpur. Agra University. J Res Sci. 9: 31–40.
- Pillai AK and Agnihotri M. 2013. Biology and predatory potential of Eocanthecona furcellata (Wolff.) on Maruca vitrata Geyer. Madras J Agric Sci. 100: 193–195.
- Siddaiah AA and Devi AR. 2015. Biology of a predatory bug Eocanthecona furcellata Wolff (Hemiptera: Pentatomidae) on Vapourer tussock moth larvae: a major pest of tasar silkworm food plants. Int J Indust Entomol.30(1): 26–30. https://doi.org/10.7852/ijie.2015.30.1.26
- Tuan SJ, Yeh CC, Atlihan R and Chi H. 2016. Linking life table and predation rate for biological control: A comparative study of Eocanthecona furcellata (Hemiptera: Pentatomidae) fed on Spodoptera litura (Lepidoptera: Noctuidae) and Plutella xylostella (Lepidoptera: Plutellidae). J Econ Entomol. 109(1): 13–24. https://doi.org/10.1093/jee/tov265
- Vanitha K, Raviprasad TN and Shwetha V. 2018. Life cycle of Eocanthecona furcellata Wolff. (Hemiptera: Pentatomidae) a predatory bug in cashew plantations, upon rearing on wax moth larvae. J Entomol Zool Stud.6(2): 3007–3010.
- Yi NN and Kyi W. 2000. Biological Control Research Center, Mandalay Division, Singaing Township, Paleik, Myanmar. Proceedings of the Annual Research Conference (Agricultural Sciences), Yangon, Myanmar, pp.58–73.
- Optimum density of Eocanthecona furcellata (Wolff) (Hemiptera:Heteroptera: Pentatomidae) to be considered for mass production under laboratory conditions
Authors
1 Department of Agricultural Entomology, UAS, Bengaluru – 560065, Karnataka, IN
2 Division of Germplasm Conservation and Utilization, ICAR-NBAIR, Hebbal, Bengaluru – 560024, Karnataka, IN
3 Division of Germplasm Conservation and Utilization, ICAR-NBAIR, Hebbal, Bengaluru –560024, Karnataka, IN
4 Department of Plant Pathology, UAS, Bengaluru – 560065, Karnataka, IN
5 Department of Crop Physiology, UAS, Bengaluru – 560065, Karnataka, IN
Source
Journal of Biological Control, Vol 35, No 1 (2021), Pagination: 1-5Abstract
Eocanthecona furcellata (Wolff) is a potential native predator of lepidopteran larvae that can be easily reared under laboratory conditions and released in augmentative biocontrol for management of pests in various crops. For successful mass production of any predator cannibalism under crowded rearing conditions is the major limiting factor. In the present study, attempts were made to know the ideal population considered for group rearing with minimal or no cannibalism. It was recorded that the predator population of 5 to 25 on Corcyra cephalonica (S.) and Galleria mellonella L. and 5 to 30 on Samia cynthia ricini Boisd. and Spodoptera litura F. was feasible for group rearing with higher percent survival rate when reared in different group arenas. The survival percent was higher on hosts, C. cephalonica, G. mellonella, S. litura and recorded lower on S. cynthia ricini under group rearing condition.
Keywords
Corcyra cephalonica, Eocanthecona furcellata, Galleria mellonella, Group Rearing, Optimum Density, Samia cynthia ricini, Spodoptera lituraReferences
- Ahirwar R, Devi P, Gupta R. 2015. Seasonal incidence of major insect-pests and their biocontrol agents of soybean crop (Glycine max L. Merrill). Sci Res Essays. 10(12): 402–406.
- Aland SR, Mamlayya AB, Kohli YJ, Bharmal DL. Bhawane GP. 2010. Studies on the heteropteran (Insecta:Heteroptera) fauna of Amba Reserved Forest, Western Ghats, Maharashtra. Bioscan. 5(3): 461–463.
- Aruna AS, Devi AR. 2015. Biology of a predatory bug E. furcellata Wolff (Hemiptera:Pentatomidae) on Vapourer tussock moth larvae: A major pest of tasar silkworm food plants. Int J Industrial Entomol. 30(1): 26–30.
- Chandrika M, Sathiamma B. 2007. Potential for lab rearing of Apanteles taragamae, the larval endoparasitoid of coconut pest Opisina arenosella, on the rice moth Corcyra cephalonica. Bio Control. 52: 747–752.
- Cherian MC, Brahmachari K. 1941. Notes on the three predatory hemipterans from South India. Indian J Entomol. 3(1): 115–119.
- De Clercq P. 2000. Predaceous stink bugs (Pentatomidae:Asopinae). Heteroptera of economic importance. CRC Press. pp. 759–812. https://doi.org/10.1201/9781420041859.ch32
- Khuhro S, Lohar M, Abro G, Talpur M, Khuhro R. 2012. Feeding potential of lady bird beetle, Brumus suturalis Fabricius (Coleoptera:Coccinellidae) on cotton mealy bug Phenococcus solenopsis (Tinsley) in laboratory and field. Sarhad J Agric. 28: 259–265.
- Meth T, Gogoi H. 2016. Rearing of Eri silkworm (Samia cynthia ricini Boisd) (Lepidoptera:Saturniidae) in Arunachal Pradesh: A study in Papumpare district. J Bio Resources. 3: 46–52.
- Metwally HM, Hafez GA, Hussein MA, Hussein MA, Salem HA, Saleh MME. 2012. Low cost artificial diet for rearing the greater wax moth, Galleria mellonella L. (Lepidoptera:Pyralidae) as a host for entomopathogenic nematodes. Egypt J Biol Pest Co. 22(1): 15.
- Mohamed MA, Coppel HC. 2017. Mass rearing of the greater wax moth, Galleria mellonella (Lepidoptera:Pyralidae), for small-scale laboratory studies. Great Lakes Entomol. 16(4): 7.
- Nabapure SM, Agnihotri M. 2011. Canthecona furcellata: A predator of Maruca vitrata. Ann Plant Prot Sci. 19: 451–508.
- Prasad D, Singh KM, Singh RN, Mehto DN. 1983. A new predator of a new pest of jasmine in Delhi. Bull. Entomol. 24: 140–141.
- Sharma AK, Bisem S, Bisem UK. 2015. Comparative analysis on activity of major predatory and insect pest species of paddy in two distinct (formincal) locations through light trap. Ecoscan. 9(1): 81–84.
- Shorey MM, Hale LL. 1965. Mass rearing of the larvae of nine noctuid species on a simple artificial medium. J Econ Entomol. 58: 522–524.
- Usha Rani P, Vukkala IH. 1993. Predatory and Mating Behaviour of Eocanthecona furcellata (Wolff.) (Heteroptera:Pentatomidae) a Promising Natural Enemy of Lepidopterous Larvae. Biol Control. 7(1): 9–11.
- Wadaskar PS, Jethva DM, Vigneswara S, Rode NS. 2015. Studies on effect of temperature and relative humidity on biology of rice moth Corcyra cephalonica (Stainton) under laboratory condition. Ecoscan. 9(1,2): 201–204.
- Wakamura S. 1988. Rearing of the beet armyworm, Spodoptera exigua (Hubner) (Lepidoptera:Noctuidae), on an artificial diet in the laboratory. Japanese J Appl Entomol Zool. 32(4): 329–331. https://doi.org/10.1303/jjaez.32.329
- Yasuda T. 2000. Role of semio-chemicals in preylocating behaviour of a generalist predatory stink bug, Eocanthecona furcellata (Wolff) (Heteroptera:Pentatomidae). Japan Agri Res. 34(1): 15–20.
- Yi NN, Kyi W. 2000. Biological Control Research Centre, Mandalay Division, Singaing Township, Paleik, Myanmar. Proceedings of the Annual Research Conference (Agricultural Sciences), Yangon, Myanmar,
- -5 April, pp. 58–73.