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Pre-Imaginal Development of Different Prey Species on the Life History Parameters of Different Species of Green Lacewings (Neuroptera: Chrysopidae)

PJAR_32_2_317-324

 

 

 

Research Article

Pre-Imaginal Development of Different Prey Species on the Life History Parameters of Different Species of Green Lacewings (Neuroptera: Chrysopidae)

Shafique Ahmed Memon1,6, Arif Ali1*, Mehar-un-Nisa Narejo2, Ghulam Khaliq3, Imran Ali Rajput4, Muhammad Adeel1, Khalil Ahmed Memon5, Dzolkhifli Omar6, Muhammad Rashid7 and Abdul Rasool5

1Department of Entomology, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Balochistan, Pakistan; 2Department of Crop Physiology, Faculty of Crop Production, Sindh Agriculture University, Tando Jam, Pakistan; 3Department of Horticulture, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Balochistan, Pakistan; 4Arid Zone Research Institute (PARC) Umerkot, Sindh, Pakistan; 5Department of Entomology, Faculty of Crop Protection, Sindh Agriculture University, Tandojam, Pakistan; 6Department of Plant Protection, Faculty of Agriculture, University Putra Malaysia; 7Department of Agronomy, faculty of agriculture,Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Balochistan, Pakistan.

Abstract | Green lacewings as predators have a wide prey range, but not all preys are equally suitable for a single lacewing. Studies were carried out to evaluate the suitability of three aphid species on the pre-imaginal development of three species of green lacewings. Developmental stages of three different species of green lacewings, Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp. were provided with three different prey species, Aphis craccivora, Rhopalosiphum maidis and Corcyra cephalonica under the laboratory conditions (25±2 °C). The results indicated that a significantly increased pre-imaginal (19.93±0.24) and mean average days (70.33±0.55) of C. nipponensis on R. Maidis and also a significantly increased pre-imaginal (20.84±0.49), (21.22±0.97) and mean average days (74.18±0.33), (68.72±0.30) of P. ramburi and Apertochrysa sp. on the host of R. maidis. Whereas a significantly decreased pre-imaginal and total mean average days were observed on C. cephalonica in all species of green lacewings. A maximum fecundity of Apertochryca sp. (645.70±8.53), C. nipponensis (618.70±12.23) and P. ramburi (590.66±5.29) were found on the host of C. cephalonica while lowest fecundity of P. ramburi (508.17± 6.91), Apertochryca sp. (517.10± 8.13) and C. nipponensis (581.10± 10.91) were observed on R. maidis.


Received | January 22, 2019; Accepted | February 16, 2019; Published | March 23, 2019

*Correspondence | Arif Ali, Department of Entomology, Lasbela University of Agriculture, Water and Marine Sciences, Uthal, Balochistan, Pakistan; Email: arifalirao@mail.com

Citation | Memon, S.A., A. Ali, M.N. Narejo, G. Khaliq, I.A. Rajput, M. Adeel, K.A. Memon, D. Omar, M. Rashid and A. Rasool. 2019. Pre-imaginal development of different prey species on the life history parameters of different species of green lacewings (Neuroptera: Chrysopidae). Pakistan Journal of Agricultural Research, 32(2): 317-324.

DOI | http://dx.doi.org/10.17582/journal.pjar/2019/32.2.317.324

Keywords | Green lacewings, Pre-imaginal development, Survival, Adult longevity and fecundity



Introduction

Human interests are always threatened by the presence of pest and pesticides as the most extensively applied methods for pest control. Approximately 2.7 million tons of pesticides were applied in the world in 2011 to control noxious pests (FAOSTAT, 2013) however, pesticide usage has many adverse effects on human and their environment, often results in pest resurgence and the killing of non-target and beneficial individuals (Weathersbee and Mckenzie, 2005). Moreover, either directly or indirectly, pesticides are responsible for over 25 million cases of pesticides poisoning and 20,000 unintended death (Hajek, 2004; Ulhaq et al., 2006) considering these adverse impacts, scientists always strive for alternate methods to control pests that could provide better pest management with less hazardous to humans and their environment.

Biological control is a method to control pests through the use of natural enemies as it is environmentally sound and economically efficient in mitigating the pest densities (Sarwar et al., 2012, 2013a, 2013b, 2014). The natural enemies are used in classical, augmentative and inundative biological control programs (Tuusalo, 1984). During recent years, the use of biological control agents such as green lacewings has shown potential to manage pest population below their economic threshold. Accordingly, many integrated management programs with biological control as their key component have been employed against many damaging pests in various crops throughout the world (Canard et al., 1984).

Chrysopids feed on various aphid species, including Aphis glycines Matsumura (Ragsdale et al., 2011), Myzus persicae Sulzer (Pappas et al., 2007), Diuraphis noxia Mordvilko (Messina and Sorenson, 2001), Aphis gossypii Glover (Liu and Chen, 2001), Lipaphis erysimi Kalt. (Kumar and Singh, 2001), Rhopalosiphum maidis Fitch (El-Serafi et al., 2000), Aphis craccivora Koch (Saminathan et al., 1999) and Monellia caryella Fitch (Liao et al., 1985). They also feed on the eggs of Lepidoptera such as Corcyra cephalonica Stainin (Bansod and Sarode, 2000), Anagasta kuehniella Zeller (Zheng et al., 1993) and Sitotroga cerealella Olivier (López-Arroyo et al., 1999).

The green lacewing, Chrysoperla sinica (Tjeder) (Neuroptera: Chrysopidae), is distributed throughout China (Xu et al., 1999) and a key predator of many important agricultural pests (notably aphids, leafhoppers, thrips, mites and Lepidoptera) (Penney et al., 2000; Principi and Canard, 1984; Ding and Chen, 1986; Zheng et al., 1993; Atlihan et al., 2004; Wang and He, 2006; Ragsdale et al., 2011). However, the adults are not predators and feed mostly on plant nectar, honeydew and pollen (Villenave et al., 2006; Li et al., 2008). The larvae forage actively and are voracious predators of various species of prey (Xu et al., 1999; Duelli, 2001) and frequently used in augmentative and inundative biological control of agricultural pests (Zhou et al., 1991; Senior and McEwen, 2001). In order to optimize the conditions used by bio-control companies to rear predator and achieve a more cost-effective method of rearing various other species of prey and artificial diets have been used (Lee and Lee, 2005; Uddin et al., 2005; Kazemi and Mehrnejad, 2011). Therefore, it is important for the successful development of pest management programs that utilize predator as a bio-control agent to identify alternative high quality prey/food. However, there are no studies on the effect of different prey species on the pre-imaginal development and reproduction of adults of Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp. The importance of nutritional quality of the prey for these predators is also unknown. The aim of present study was to evaluate pre-imaginal development of different prey species on the life history parameters of different species of green lacewings in terms of survival, development and reproduction under laboratory conditions.

Materials and Methods

Culture of factitious host, Corcyra cephalonica

Initially the culture of rice moth, C. cephalonica was obtained from the Department of Plant Protection, University Putra Malaysia. To establish the culture of factitious host, the ingredients such as maize, rice, wheat and semolina (1:1:1:1) were autoclaved to prevent any unwanted infestation and/ or pathogens. Approximately after one hour of cooling the sterilized ingredients, they were mixed and placed in plastic cages measuring 37 × 28cm × 22cm. Eggs of C. cephalonica were spread over the diet inside the cage. Rearing conditions for culture were 25 ± 2 °C, 55-85% RH and 12L: 12D photoperiod to develop C. cephalonica to adult stage that was collected for matting in a plastic cage. The eggs produced were collected in a glass plate and placed in the freezer to exhaust egg viability.

Culture of natural preys, Aphis craccivora and Rhopalosiphum maidis

The culture of natural preys, Rhophalosiphum maidis and Aphis craccivora was established on their respective hosts in the laboratory conditions. Initially, the culture was collected from the farmer field of Ladang II, near the insectary of University of Putra Malaysia. The aphids were maintained in cages measuring 20 × 13cm × 10cm size. The top of the cages was covered with organza cloth for aeration and the rearing conditions for culture were 25 ± 2°C. The rearing of preys was carried out for one month to obtain a sufficient number of prey for the larvae of predators. Fresh host nymphs/ adults were provided to the all larval instars of green lacewing species in the petri dishes.

Culture of green lacewings, Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp.

The experimental adults of green lacewings were obtained from the colony. Adults were maintained in cylindrical glass jars (18 cm in diameter and 25 cm high). The standard adult diet was composed according to Alasady et al. (2010). It comprised of 2.5 g yeast, 3 g sugar, 2.5 ml honey, 3 g milk Begin Match to source 33 in source list: http://www.fspublishers.org/published_papers/67167_..pdfpowder (instead of casein) 2.5 ml distilled water and the mixture forms a slurry that was provided on a plastic strip in the rearing cages with measurement of 2 × 15cm. Thus, each larva of all respective species of green lacewings was reared separately Begin Match to source 25 in source list: Amarasekare, Kaushalya G., and Peter W. Shearer. in trays of ELISA wells. Rearing conditions for stock cultures of chrysopids were 25 ± 2°C.

In present study, three different species of green lacewings, Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp. were used with three different host species, Aphis craccivora, Rhopalosiphum maidis and Corcyra cephalonica to investigate the suitability of food for the immature stages. Third- and fourth instar nymphs of each aphid species were supplied daily to each species of green lacewing larvae (ad libitum 15–200 aphids according to larval age) throughout their larval development. In the case of C. cephalonica eggs, fresh eggs were supplied daily to larvae (ad libitum 50–250 eggs according to larval age). The pre-imaginal development and reproductive parameters were observed under the laboratory conditions 25±2 °C. After hatching of eggs of each green lacewing species, thirty (30) young larvae were randomly selected and provided each prey species separately Begin Match to source 25 in source list: Amarasekare, Kaushalya G., and Peter W. Shearer. in trays of ELISA wells. After reaching to the pupal stage, twenty-five (25) pupae were randomly selected from each treatment to find the pupal days and then from each treatment ten (10) pairs of adults sorted according to sex were confined to check the fecundity and longevity of both males and females. Similarly, these adults were supplied with the artificial diet described above for colony maintenance.

Statistical analysis

The software SPSS (SPSS Inc., Chicago, IL, US) was used for data analysis. The one-way analysis of variance (ANOVA) was used for analysis of data and means were compared using Tukey test at P<0.05.

Results and Discussion

A significant difference was observed in the developmental stages of green lacewing, Chrysoperla nipponensis against prey species, Rhopalosiphum maidis, whereas short developmental days of C. nipponensis were observed on the host of C. cephalonica. However, statistically no difference was observed on 1st larval instar in comparison to other treatments. The highest and significant increased fecundity was observed on the C. cephalonica and the lowest fecundity was recorded on R. maidis Table 1. A significant difference was recorded in all developmental periods of green lacewing Plesiochrysa ramburi when provided prey species, A. craccivora, while the short developmental periods of P. ramburi were observed on C. cephalonica. Statistically no significant difference was observed between the hosts of A. craccivora and R. maidis respectively. The highest number of fecundity was seen on the host of C. cephalonica and low fecundity was observed when supplied the host R. maidis as mentioned in Table 2. The developmental periods of green lacewing, Apertochrysa sp. were significantly increased when the green lacewing, Apertochrysa sp. was provided A. craccivora, although a significant decrease in life stages of Apertochrysa sp. were observed against C. cephalonica. While no significant difference was observed between 1st and 2nd instars of Apertochrysa sp. in all other treatments. Statistically maximum fecundity was observed when the host, C. cephalonica were provided, whereas the minimum fecundity was noticed on the host of A. craccivora as indicated in the Table 3. The green lacewing larvae feed on a variety of soft-bodied insects (Tauber and Tauber, 1983; Ding and Chen, 1986; Zheng et al., 1993; Rao et al., 2003; Rajabaskar, 2007) and are considered to be key predators of many agriculturally important pests (Principi and Canard, 1984; Ragsdale et al., 2011). It is widely reported that unsuitable food can extend the pre-imaginal development of chrysopids and decrease the survival, fecundity and longevity of the adults (Principi and Canard, 1984; Obrycki et al., 1989; Zheng et al., 1993). In this study we evaluated the pre-imaginal developmental period as well as adult longevity and fecundity of green lacewings, Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp. provided with different species of prey. Generally, the larvae of all species of green lacewings that were reared on factitious and natural preys had shorter pre-imaginal developmental periods and the adults lived longer and were more fecund except those

Table 1: Effect of prey species on the developmental stages on green lacewing, Chrysoperla nipponensis.

Developmental stages Different hosts of C. nipponensis ­­­­­­­­
  A. craccivora R. maidis C. cephalonica

1st instar

3.50±0.93a 3.56±0.62a 3.26±0.63a

2nd instar

3.53±0.62a 4.33±0.71b 3.43±0.68a
3rd Instar 3.50±0.50a 4.10±0.54b 3.26±0.44a
Pupal stage (days) 6.92±0.08b 8.00±0.15a 6.36±0.15c
Pre-imaginal days 17.41±0.33b 19.93±0.24a 16.41±0.20c
Male days (longevity) 46.40±1.49a 47.50±1.37a 39.50±0.83b
Female days (longevity) 54.30±1.44a 55.80±0.61a 47.20±0.80b
Total mean average (days) 68.51±0.60a 70.33±0.55a 59.76±0.37b
Fecundity 608.80±4.10ab 581.10± 10.91b 618.70±12.23a

Mean (± SE) followed by different letters within a column are significantly different by Tukey Test (P<0.05).

Table 2: Effect of prey species on the developmental stages on green lacewing, Plesiochrysa ramburi.

Developmental stages Different hosts of P. ramburi­­
  A. craccivora R. maidis C. cephalonica

1st Instar

3.90±0.81a 3.76±0.59ab 3.12±0.29b

2nd Instar

4.02±0.88a 3.96.±0.41a 3.51±0.45b
3rd Instar 3.90±0.75a 3.70±0.30a 3.02±0.20b
Pupal stage (days) 9.02±0.14a 8.85±0.27a 7.32±0.44b
Pre-imaginal days 20.84±0.49a 20.07±0.21a 17.01±0.39b
Male days (longevity) 47.20±0.19a 45.80±0.36a 40.27±0.73b
Female days (longevity) 59.49±1.26a 56.89±1.11ab 53.66±1.14b
Total mean average (days) 74.18±0.33a 71.41±0.88a 63.97±0.80b
Fecundity 533.40±3.18b 508.17± 6.91b 590.66±5.29a

Mean (± SE) followed by different letters within a colum are significantly different by Tukey Test (P<0.05).

Table 3: Effect of prey species on developmental stages on green lacewing, Apertochrysa sp.

Developmental stages Different hosts of Apertochrysa sp.
  A. craccivora R. maidis C. cephalonica

1st Instar

4.10±0.11a 3.90±0.37a 3.96±0.23a

2nd Instar

3.90±0.19a 3.80±0.31ab 3.66±0.28a
3rd Instar 4.30±0.15a 4.10±0.39a 3.26±0.14b
Pupal stage (days) 8.92±0.81a 8.60±0.49a 7.48±0.39b
Pre-imaginal (days) 21.22±0.97a 20.40±0.38a 18.09±0.26b
Male days (longevity) 43.10±0.69a 42.89±0.17a 40.15±0.66b
Female days (longevity) 51.60±1.38a 52.18±1.19a 49.00±1.29b
Total mean average (days) 68.72±0.30a 67.93±0.42a 62.66±0.44b
Fecundity 554.25±9.19c 517.10± 8.13b 645.70±8.53a

Mean (± SE) followed by different letters within a column are significantly different by Tukey Test (P<0.05).

reared-on C. cephalonica. This indicates that the species of prey is of paramount importance as part of a balanced source of food (Evans et al., 1999) to ensure the nutrients that enhance the pre-imaginal developmental period and the longevity and fecundity of the later stages of green lacewings. However, rearing of different species of green lacewings on range of different species of prey resulted in little variation, which might indicate that these predators are well adapted to these particular natural prey niches. The shorter pre-imaginal period of larvae of P. ramburi and Apertochrysa sp. was observed when supplied with nymphs of R. maidis as compared to A. craccivora that accords with the results of Obrycki et al. (1989), who reported that larvae of Chrysopa oculata Say take less time to develop when reared on R. maidis. Above all, rearing of green lacewings, Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp. on C. cephalonica eggs resulted in higher fecundity as compared to those reared on aphids, as previously recorded by Wang and Nordlund (1994); Pappas et al. (2007); Huang and Enkegaard (2009), suggesting that eggs are very nutritious. This probably indicates variations among predators in their physiological responses to the different nutrient contents of prey and such difference might be due to differences among the species in their nutritional requirements (El-Arnaouty et al., 1994). Finally, our study indicates that of all the prey tested the eggs of rice moth, C. cephalonica, are the most suitable food for the mass rearing of all three species of green lacewings, Chrysoperla nipponensis, Plesiochrysa ramburi and Apertochrysa sp. However, further studies are required to evaluate the field performance of these predators in Malaysia in terms of feeding on aphids when they are mass reared on the eggs of Lepidoptera.

Conclusions and Recommendations

In present investigation we observed that significantly increased developmental stages of green lacewing species Plesiochrysa ramburi and Apertochrysa sp. on the host of A. craccivora, and longer duration of Chrysoperla nipponensis were seen on the host of R. maidis. However, shorter developmental stages of all green lacewing species were found on the host of C. cephalonica. Similarly, the highest fecundity of all green lacewing species was observed on the host of C. cephalonica and minimum fecundity were seen on the host of R. maidis. This might be due to the high level of protein in eggs of C. cephalonica that green lacewing is able to complete their life cycle in earlier days and also support them for increasing fecundity in short duration. Moreover, this information would be helpful for optimizing the mass rearing of predators and for understanding its population dynamics in the field in the presence/absence of the various species of prey tested.

Acknowledgement

This research was financially supported by University Putra Malaysia’s research grant (number 63236). It is a pleasure to acknowledge all the authors whose meticulous and detailed work was cited in this paper.

Author’s Contributions

S.A. Memon conceived the idea of data collection and overall management of the manuscript, A. Ali and I.A. Rajput analyzed the data, M.N. Narejo, worked on plagiarism, K. Ghulam, Reviewed the manuscript. M. Adeel and K.A. Memon contributed to format the manuscript according to the standard of journal. O. Dzolkhifli provided technical inputs at every step of this work.

References

Alasady, M.A., A. Omar, D. Ibrahim and R. Ibrahim. 2010. Life table of the green lacewing Apertochrysa sp. (Neuroptera: Chrysopidae) reared on rice moth Corcyra cephalonica (Lepidoptera: Pyralidae). Int. J. Agric. Bio. 12(2): 266-270.

Atlihan, R., B. Kaydan and M.A. Özgökçe. 2004. Feeding activity and life history characteristics of the generalist predator, Chrysoperla carnea (Neuroptera: Chrysopidae) at different prey densities. J. Pest. Sci. 77: 17–21. https://doi.org/10.1007/s10340-003-0021-6

Bansod, R.S. and S.V. Sarode. 2000. Influence of different prey species on biology of Chrysoperla carnea (Stephens). Shashpa. 7: 21–24.

Canard, M., Y. Semeria and T.R. New. 1984. Biology of chrysopidae, Dr. W. Junk publishers. The hague. pp. 294.

Ding, Y.Q. and Y.P. Chen. 1986. Predation pattern of Chrysoperla sinica (Chrysopa) on cotton, aphid and cotton bollworm. Chin. J. Biol. Control. 2: 97–102.

Duelli, P. 2001. Lacewings in field crops. In: pp. 158-171: Lacewings in the crop environment, P.K. McEwen, T.R. New and A.E. Whittington. Cambridge Univ. Press. Cambridge, UK. https://doi.org/10.1017/CBO9780511666117.010

El-Serafi, H.A.K., A.H. Abdel-Salam and N.F. Abdel-Bakey. 2000. Effect of four aphid species on certain biological characteristics and life table parameters of Chrysoperla carnea (Stephens) and Chrysoperla septempunctata Wesmael (Neuroptera: Chrysopidae) under laboratory conditions. Pak. J. Biol. Sci. 3: 239–245. https://doi.org/10.3923/pjbs.2000.239.245

El-Arnaouty, S.A., A. Ferran and V. Beyssat-Arnaouty. 1996. Food consumption by Chrysoperla carnea (Stephens) and Chrysoperla sinica (Tjeder) of natural and substitute prey: determination of feeding efficiency (Insecta: Neuroptera: Chrysopidae). In M. Canard, H. Aspöck and M.W. Mansel. (eds): Pure and applied research in neuropterology. Proce. 5th Int. Symp. Neuropterol., Cairo, 2–6 May 1994. Sacco, Toulouse, pp. 109–117.

El-Arnaouty, S. A., A. Ferran, and V. Beyssat-Arnaouty. 1994. Food consumption by Chrysoperla carnea (Stephens) and Chrysoperla sinica (Tjeder) of natural and substitute prey: determination of feeding efficiency (Insecta: Neuroptera: Chrysopidae).” Pure and Applied Research in Neuropterology. Proceedings of the 5th International Symposium on Neuropterology, Cairo. pp. 2-6.

Evans, E.W., A.T. Stevenson and D.R. Richard. 1999. Essential versus alternative foods of insectpredators: benefit of mixed diets. Oecologia. 121: 107–112. https://doi.org/10.1007/s004420050911

FAOSTAT. 2013. World pesticed use. Food Agric. Organ. U.N. http://faostat.fao.org. Accessed on November 12, 2015.

Huang, N. and A. Enkegaard. 2009. Predation capacity and prey preference of Chrysoperla carnea on Pieris brassicae. Bio Control. 55: 379–385. https://doi.org/10.1007/s10526-009-9254-5

Hajek, A. 2004. Natural enemies an introduction to biological control. USA: Cambridge Univ. Press. pp. 378. https://doi.org/10.1017/CBO9780511811838

Kazemi, F. and M.R. Mehrnejad. 2011. Seasonal occurrence and biological parameters of the common green lacewing predators of the common Pistachio psylla, Agonoscena pistaciae (Hemiptera: Psylloidea). Eur. J. Entomol. 108: 63–70. https://doi.org/10.14411/eje.2011.008

Kumar, S. and S. Singh. 2001. Effectiveness and economics of different treatments against mustard aphid, Lipaphis erysimi (Kalt.) in mustard crop. Journal of Entomological Research, 25(2). Pp.127-129.

Li, Y., M. Meissle and J. Romeis. 2008. Consumption of Bt maize pollen expressing Cry1Ab or Cry3Bb1 does not harm adult green lacewings, Chrysoperla carnea (Neuroptera: Chrysopidae). PLoS One. 3(8): e2909. https://doi.org/10.1371/journal.pone.0002909

Lee, K.S. and J.H. Lee. 2005. Rearing of Chrysopa pallens (Rambur) (Neuroptera: Chrysopidae) on artificial diet. Entomol. Res. 35: 183–188. https://doi.org/10.1111/j.1748-5967.2005.tb00157.x

López-Arroyo, J.I., C.A. Tauber and M.J. Tauber. 1999. Effects of prey on survival, development and reproduction of trash carrying chrysopids (Neuroptera: Ceraeochrysa). Environ. Entomol. 28: 1183–1188. https://doi.org/10.1093/ee/28.6.1183

Liao, H.T., M.K. Harris, F.E. Gilstrap and F. Mansour. 1985. Impact of natural enemies on the black margined pecan aphid, Monellia caryella (Homoptera: Aphidae). Environ. Entomol. 14: 122–126. https://doi.org/10.1093/ee/14.2.122

Liu, T.X. and T.Y. Chen. 2001. Effects of three aphid species (Homoptera: Aphididae) on development, survival and predation of Chrysoperla carnea (Neuroptera: Chrysopidae). Applied Entomology and Zoology, 36(3), 361-366.

Messina, F.J. and S.M. Sorenson. 2001. Effectiveness of lacewing larvae in reducing Russian wheat aphid populations on susceptible and resistant wheat. Biol. Control. 21: 19–26. https://doi.org/10.1006/bcon.2000.0914

Obrycki, J.J., M.N. Hamid, A.S. Sajap and L.C. Lewis. 1989. Suitability of corn insect pest for development and survival of Chrysoperla carnea and Chrysoperla oculata (Neuroptera: Chrysopidae). Environ. Entomol. 18: 1126–1130. https://doi.org/10.1093/ee/18.6.1126

Pappas, M.L., G.D. Broufas and D.S. Koveos. 2007. Effects of various prey species on development, survival and reproduction of the predatory lacewing Dichochrysa prasina (Neuroptera: Chrysopidae). Biol. Control. 43: 163–170. https://doi.org/10.1016/j.biocontrol.2007.07.006

Penny, N.D., C.A. Tauber and T. Deleon. 2000. A new species of Chrysopa from western North America with a key to North American species (Neuroptera: Chrysopidae). Ann. Entomol. Soc. Am. 93(4): 776-784. https://doi.org/10.1603/0013-8746(2000)093[0776:ANSOCF]2.0.CO;2

Principi, M.M. and M. Canard. 1984. Feeding habits. In: M. Canard, Y. Semeria and T.R. New. (Eds.), Biology of chrysopidae. Dr. W. Junk, The hague. pp. 76-92.

Ragsdale, D.W., D.A. Landis, B. Jacques, G.E. Heimpel and N. Desneux. 2011. Ecology and management of the soybean aphid in North America. Annu. Rev. Entomol. 56: 375–379. https://doi.org/10.1146/annurev-ento-120709-144755

Rajabaskar, D. 2007. Stage preference and predatory potential of the bug Chrysoperla carnea against jasmine leaf webworm, Nausinoe geometralis. J. Ecobiol. 19: 97–99.

Rao, C.N., V.J. Shivankar and S. Shyam. 2003. Predatory potential and development of the green lacewing (Mallada boninensis) on citrus leaf-miner (Phyllocnistis citrella). India. J. Agric. Sci. 73: 60–61.

Sarwar, M. 2013a. Management of spider mite Tetranychus cinnabarinus (Boisduval) (Tetranychidae) infestation in cotton by releasing the predatory mite Neoseiulus pseudolongispinosus (Xin, Liang and Ke) (Phytoseiidae). Bio. Control. 65(1): 37-42. https://doi.org/10.1016/j.biocontrol.2012.09.017

Sarwar, M. 2013b. Comparing abundance of predacious and phytophagous mites (Acarina) in conjunction with resistance identification between Bt and non-Bt cotton cultivars. Afri. Entomol. 21(1): 108-118. https://doi.org/10.4001/003.021.0124

Sarwar, M. 2014. Influence of host plant species on the development, fecundity and population density of pest Tetranychus urticae Koch (Acari: Tetranychidae) and predator Neoseiulus pseudolongispinosus (Xin, Liang and Ke) (Acari: Phytoseiidae). N. Z. J. Crop Horti. Sci. 42(1): 10-20. https://doi.org/10.1080/01140671.2013.817444

Sarwar, M., X. Xuenong and W. Kongming. 2012. Suitability of webworm Loxostege sticticalis L. (Lepidoptera: Crambidae) eggs for consumption by immature and adults of the predatory mite Neoseiulus pseudolongispinosus (Xin, Liang and Ke) (Acarina: Phytoseiidae). Span. J. Agri. Res. 10(3): 786-793. https://doi.org/10.5424/sjar/2012103-461-11

Senior, L.J. and P.K. Mcewen. 2001. The use of lacewings in biological control. In McEwen P.K., New T.R and Whittington A.E. (eds): Lacewings in the Crop Environment. Cambridge Univ. Press Cambridge. pp. 296–302. https://doi.org/10.1017/CBO9780511666117.014

Saminathan, V.R., R.K.M. Baskaran and N.R. Mahadevan. 1999. Biology and predatory potential of green lacewing (Chrysoperla carnea) (Neuroptera: Chrysopidae) on different insect hosts. India. J. Agric. Sci. 69: 502–505.

Tuusalo, U. 1984. Mass rearing techniques, In: Canard M., Semeria Y. and T. R. New (Eds), Biology of Chrysopidae, pp. 213- 220. W. Junk, Dordrecht.

Tauber, M.J. and C.A. Tauber. 1983. Life history traits of Chrysopa carnea and Chrysopa rufilabris (Neuroptera: Chrysopidae): Influence of humidity. Ann. Entomol. Soc. Am. 76: 282–285. https://doi.org/10.1093/aesa/76.2.282

Ulhaq, M.M., A. Sattar, Z. Salihah, A. Farid, A. Usman and S.U.K. Khattak. 2006. Effect of different artificial diets on the biology of adult green lacewing (Chrysoperla carnea) Stephens Songkanakarin. J. Sci Tech. 28: 1-8.

Uddin, J., N.J. Holliday and P.A. Mackay. 2005. Rearing lacewings, Chrysoperla carnea and Chrysopa oculata (Neuroptera: Chrysopidae), on prepupae of alfalfa leafcutting bee, Megachile rotundata (Hymenoptera: Megachilidae). Proc. Entomol. Soc. Manitoba. 61: 11–19.

Villenave, J., B. Deutsch, T. Lodé and E. Rat-Morris. 2006. Pollen preference of the Chrysoperla species (Neuroptera: Chrysopidae) occurring in the crop environment in western France. Eur. J. Entomol. 103: 771–777. https://doi.org/10.14411/eje.2006.104

Wang, W.J. and H.E.D.H. 2006. Research of the control role of three primary natural enemies to Tetranychus urticae (Koch). Chin. J. Agric. Sci. 27: 16–19.

Weathersbee, A.A. and C.L. McKenzie. 2005. Effect of a neem biopesticide on repellency, mortality, oviposition, and development of Diaphorina citri (Homoptera: Psyllidae). Fla. Entomol. 88: 401-407. https://doi.org/10.1653/0015-4040(2005)88[401:EOANBO]2.0.CO;2

Wang, R. and D.A. Nordlund. 1994. Use of Chrysoperla spp. (Neuroptera: Chrysopidae) in augmentative release programmes for control of arthropod pests. Biocontrol News Inf. 15: 51–57.

Xu, Y., J. Mu and C. Hu. 1999. Research and utilization of Chrysoperla sinica. Entomol. Knowl. 36: 313–315.

Zheng, Y., K.S. Hagen, K.M. Daane and T.E. Mittler. 1993. Influence of larval dietary supply on the food consumption,food utilization efficiency, growth and development of lacewing Chrysoperla carnea. Entomol. Exp. Appl. 67: 1– 7. https://doi.org/10.1111/j.1570-7458.1993.tb01644.x

Zhou, W.R., R. Wang and S.B. Qiu. 1991. Field studies on the survival of Chrysoperla sinica (Neuroptera: Chrysopidae) mass reared and inoculatively released in wheat fields in Northern China. Chin. J. Biol. Control. 7: 97–100.

Pakistan Journal of Agricultural Research

September

Vol.37, Iss. 3, Pages 190-319

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