Journal of Iranian Plant Protection Research

Journal of Iranian Plant Protection Research

Comparison of Efficiency of the Predatory Mite Neoseiulus californicus (Acari: Phytoseiidae) Reared on Several Plant Pollens

Document Type : Research Article

Author
Zoology Research Department, Iranian Research Institute of Plant Protection, Agricultural Research, Education and Extension Organization (AREEO), Tehran, Iran
Abstract
Introduction
The predatory mite Neoseiulus californicus (McGregor) is an effective predator for the control of many pests, especially in greenhouses. Evaluation of mass rearing of biological agents has several objectives and strategies, and predator quality control plays a key role in the use of these biological agents. Pollen can be used as an available food source for the rearing and mass production of phytoseiid mites. The nutritional value of pollen varies between plant species. In this study, the efficiency of the predatory mites reared on several plant pollens (corn, palm, sunflower, and walnut pollen) and different developmental stages of the storage mite Tyrophagus putrescentiae (Schrank) (Acari: Acaridae) was investigated. Evaluate the effectiveness of the predatory mites, it is necessary to examine characteristics such as host preference, predation rate, and functional response.
 
Material & Methods
The female predatory mites N. californicus from the rearing colonies were placed on strawberry leaf discs (2 × 2 cm2) with 50-60 spider mite eggs and the number of spider mite eggs after 24 hours was counted. The predation rate of the predatory mites reared on tested pollen and storage mites for one, five, and 20 generations from Tetranychus urticae Koch (Acari: Trtranychidae) eggs was compared. In another test, the predation rate of individuals reared on tested pollen from different life stages of the two-spotted spider mite was compared. The host preference of the populations of different life stages of the two-spotted spider mite were also investigated. The Manley method was used to determine the host preference of the predatory mite. The functional response of three-day old mated female from the rearing colonies feeding on densities of T. urticae eggs (2, 4, 8, 16, 32, 45, 60 and 70) was studied on strawberry leaves. These tests were conducted under laboratory condition (27±1˚C, 16L: 8D photoperiod and 70-80% RH).
 
Results & Discussion
The results showed that the duration of rearing of the predatory mite had no significant effect on the predation rate. The lowest predation rate of spider mite nymphs and adults was reported for individuals reared on sunflower pollen. Among prey life stages, adults in reared populations of N. californicus mites showed a greater preference for protonymphs, while no differences were observed between populations. The handling time among the tested populations was different, and the shortest time for the predatory mites reared on sunflower pollen and corn pollen. There is a significant difference in the predation rate of predatory mites on eggs, nymphs and adults of spider mites. The highest predation rate is on spider mites nymphs. The presence of pollen in the rearing containers has caused a significant difference in the predation rate of predatory mites on two-spotted spider mite eggs. The calculated Manley ß index of predatory mite populations on different life stages of spider mites is significant. The functional response of the predatory mite on sunflower pollen, palm pollen, walnut pollen populations exhibited type Π and on the spider mites and corn pollen populations exhibited type Ш. The Rogers equation was used to determine the statistics of attack coefficient (a, b) and handling time (Th). The attack coefficient for the predatory mite N. californicus reared on sunflower pollen, palm pollen and walnut pollen was estimated to be 0.057±0.020, 0.180±0.017 and 0.077±0.023, respectively. The handling time and attack coefficient (b) for populations of predatory mites N. californicus reared on corn pollen and two-spotted spider mite eggs were estimated to be (1.360±0.220 h and 0.100±0.090) and (2.370±0.210 h and 0.170±0.010), respectively. Using the combined equation, the functional response statistics were compared and it was found that the handling time of predatory mites in different rearings was significantly different from each other. The shortest time for a predatory mite to reach prey is in mites reared on sunflower pollen and corn pollen.
 
Conclusion
The time to reach prey varies among the populations tested, and the shortest time for the predatory mites to reach prey is in mites reared on sunflower pollen and corn pollen. The use of walnut pollen and palm pollen in addition to different life stages of the storage mite T. putrescentiae is suitable for mass and semi-mass rearing of the predatory mite N. californicus. The efficiency of reared mites in terms of predation rate from preferred prey was also better in populations reared on walnut pollen or palm pollen with storage mites than in other cases studied, and their use is recommended for rearing predatory mites. The use of walnut and palm pollen with different life stages of the storage mite T. putrescentiae is suitable for mass and semi-mass rearing of N. californicus. The efficiency of reared mites in terms of predation rate from preferred prey was also better in populations reared on walnut pollen or palm pollen with storage mites than in other cases studied, and their use is recommended for rearing predatory mites.
Keywords
Subjects

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Badi, M. H., McMurtry, J. A., & Flores, A. E. (1999). Rates of development, survival and predation of immature stages of Phytoseiulus Longipes (Acari: Mesostigmata: Phytoseiidae). Experimental Applied Acarology, 23, 611-621. https://doi.org/10.1023/A:1006179323636
Blackwood, J. S., Schausberger, P., Croft, B. A. (2001). Prey- stage preference in generalist and specialist phytoseiid mite (Acari: phytoseiidae) when offered Tetranychus urticae (Acari: Tetranychidae) eggs and larvae. Environmental Entomology, 30, 1103-1111. https://doi.org/10.1603/0046-225X-30.6.1103
Canlas, L., Amano, H., Ochiai, N., & Takeda, M. (2006). Biology and predation of the Japanese strain of Neoseiulus californicus (Acari: Phytoseiidae). Systematic & Applied Acarology, 11, 141-157. https://doi.org/10.11158/saa.11.2.2
Castagnoli, M., & Simoni, S. (1999). Effect of long-term feeding history on functional and numerical response of Neoseiulus californicus (Acari: Phytoseiidae). Experimental Applied Acarology, 23, 217-234. https://doi.org/10.1023/A:1006066930638
Coll, M., & Ridgway, R. L. (1995) Functional and numerical responses of Orius insidiosus (Heteroptera: Anthocoridae) to its prey in different vegeta Ble crops. Annals of the Entomological Society of America, 88, 732-738. https://doi.org/10.1093/aesa/88.6.732
Croft, B. A., Monetti, L. N., & Pratt, P. D. (1998). Comparative life histories and predation types: Are Neoseiulus californicus and N. fallacies (Acari: Phytoseiidae) similar type II selective ality control of mass– reared arthropods: Nutritional effects on performanance of predatory mites. Experimental Applied Acarology, 108, 462-475. https://doi.org/10.1093/ee/27.3.531
De Clercq, P., Mohaghegh, J., & Tirry, L. (2000) Effect of host plant on the functional response of the predator Podisus nigrispinus (Heteroptera: Pentatomidae). Biological Control, 18, 65-70. https://doi.org/10.1006/bcon.1999.0808
De Moraes, G. J., McMurtry, J. A., Denmark, H. A., & Campos, C. B. )2004(. A revised catalog of the mite family Phytoseiidae. Magnolia Press, Auckland. 494 pp. https://doi.org/10.11646/zootaxa.434.1.1
Farazmand, A., Fathipour, Y., & Kamali, K. (2012). Functional response and mutual interference of Neoseiulus californicus and Typhlodromus bagdasarjani (Acari: Phytoseiidae) in Tetranychus urticae (Acari: Tetranychidae). International Journal of Acarology, 38(5), 369-376. https://doi.org/10.1080/01647954.2012.655310
Friese, D. D., & Gilstrap, F. E. (1982). Influence of prey availability on reproduction and prey consumption of Phytoseiulus persimilis, Amblyseius californicus, and Metaseiulus occidentalis (Acarina: Phytoseiidae). International Journal of Acarology, 1982(8), 85-89. https://doi.org/10.1080/01647958208683283
Hatherly, L. S., Bale, J. S., & Walters, K. F. A. (2005). Intraguild predation and feeding preferences in three species of phytoseiid mite used for biological control. Experimental Applied Acarology, 37, 43-55. https://doi.org/10.1007/s10493-005-0358-z
Helle, W., & Overmeer, W. P. J. (1985). Rearing techniques. In: W. M. Helle & W. Sablis (Eds.) Spider Mites: Their Biology. Elsevier, Amsterdam. Natural Enemies and Control, 1a, 331-335.
Kostiainen, T., & Hoy, M.A. (1994). Egg-harvesting allows large scale rearing of Amblyseius finlandicus (Acari: Phytoseiidae) in the laboratory. Experimental Applied Acarology, 18, 155-165. https://doi.org/10.1007/BF02353683
Hokkanen, H. M. T. (1989) Choosing an effective biocontrol agant - an evolutionary prespeetive. Acta Entomologica Fennica, 53, 19-24.
Laing, J. E., & Osborn, J. A. L. (1974). The effect of prey density on functional and numerical response of three species of predatory mites. Entomophaga, 19, 267-277. https://doi.org/10.1007/bf02371052
Lester, P. J., & Harmsen, R. (2002). Functional and numericalresponses do not always indicate the most effectivepredator for biological control: An analysis of two predatorsin a two-prey system. Journal of Applied Ecology, 39, 455-468. https://doi.org/10.1046/j.1365-2664.2002.00733.x
Luck, R. F. (1990). Evaluation of natural enemis for biological control: A behavioral evaluation. Trends  of Ecology Evoltion.  In: U. Gerson, R. L. Smiley, & R. Ochoa (Eds). Mites (Acari) For Pest Control. Blackwell Science Ltd, Oxford, Uk, 539 p.
Jervis, M., & Kidd, K. (1996). Insect natural enemy’s practical approaches to their study and evaluation, 1st Edition. Chapman & Hall. London.
Jeschke, J. M., Kopp, M., & Tollrian, R. (2002). Predator functional responses: Discriminating between handling and digesting prey. Ecological Monographe, 72(1), 95-112. https://doi.org/10.1890/0012-9615(2002)072[0095:PFRDBH]2.0.CO;2  
Juliano, S. A. (2001). Nonlinear curve-fitting, predation and functional n and Analysis of Ecolresponse curves. In: S. M. Scheiner & J. Gurevitch (Eds.). Desigogical Experiment. Oxford University Press. New York.432 p. https://doi.org/10.1093/oso/9780195131871.003.0010  
Manly, B. F. J. (1974). A model for certain types of selection experiments. Biometrics, 30, 281-294. https://doi.org/10.2307/2529649
Marafel, P. P., Reis, P. R., Silveira, E. C., Toledo, M. A., & Souza-Pimentel, G.C. (2011). Neoseiulus californicus preying in different life stages Tetranychus urticae (Acari: Phytoseiidae, Tetranychidae). Acarologia, 51, 499- 506. https://doi.org/10.1051/acarologia/20112031ff .
Messina, F. J., & Hanks, J. B. (1998). Host plant alters the shape of functional response of an aphid predator (Coloptera: Coccinellidae). Environmenyal Entomology, 27, 1196-1202. https://doi.org/10.1093/ee/27.5.1196
McMurtry, J. A., & Croft, B. A. (1997). Life-styles of phytoseiid mite and their roles in biological control. Annual Review of Entomology, 42, 291-321. https://doi.org/10.1146/annurev.ento.42.1.291
Murdoch, W. W. (1969). Switching in general predators experiments on predator specificity and stability of prey populations. Ecological Monographe, 39(4), 335-354. https://doi.org/10.2307/1942352
Nomikou, M., Janssen, A., & Sabelis, M. W.)  2003(. Phytoseiid predators of whiteflies feed and reproduce on non-prey food source. Experimental Applied Acarology, 31, 15-26. https://doi.org/10.1023/b:appa.0000005142.31959.e8.
Norbakhesh, S. (2023). List of important pests, diseases and weeds of major agricultural crops, pesticides and recommended methods for their control. Plant Protection Organization.Tehran, 226 p.
Rezaie, M., Saboori, A., & Baniameri, V. (2017). The effect of strawberry cultivars on functional culticvars on functional response and prey- stage pereference of Neoseiulus californicus (Acari: Phytoseiidae) on Tetranychus urticae (Acari: Tetranychidae). Journal of Entomology and Zoology Studies, 5(1), 27-35.
Rogers, D. J. (1972). Random search and insect population models. Journal of Animal Ecology, 41(2), 369-383. https://doi.org/10.2307/3474
Rott, A. S, & Ponsonby, D. J. (1998). The effect of temperature, relative humidity and host plant on the behaviour of Amblyseius californicus as a predator of the two-spotted spider mite (Tetranychus urticae). The Proceedings of the British Crop Protection Council International Conference: Pests and Diseases. vol 3. Brighton. 807-812 pp.
Sabelis, M. W. (1985). Reproductive strategies: In: W. Helle & M. W. Sabelis (Eds). Spider Mites. Their Biology, Natural Enemies and Controls, Vol. 1A. Elsevier. Amsterdam. pp. 265-278.
Samaras, K., Pappas, M. L., Pekas, A., Wackers, F., & Broufas, G. D. (2021). Benefits of a balanced diet? Mixing prey with pollen is advantageous for the phytoseiid predator Amblydromalus limonicus. Biological Control, 155, 104531, https://doi.org/10.1016/j.Biocontrol.2021.104531 .
SAS, Inc. (2003). Version 9.1. SAS Institute Inc. Cary. Nc. USA.
Shimoda, T., Kishimoto, H., Takabayashi, J., Amano, H., & Dicke, M. (2009). Comparison of thread-cutting behavior in three specialist predatory mite to cope with complex webs of Tetranychus spider mitte. Experimental Applied Acarology, 47, 111-120. https://doi.org/10.1007/s10493-008-9205-3
SPSS Inc.) 2012 .(IBM SPSS Statistics for Windows, version 21.0. Armonk, NY: IBM Crop
Steiner, M. Y. (1993). Some observations on the quality of biological control organisms used in greenhouses. IOBC/WPRS Bulltein, 16, 165-168.
Swirski, E., Amitai, S., & Dorzia, N. (1970). Laboratory studies on the feeding habits, post-embryonic survival and oviposition of the predaceous mites Amblyseius chilenensis Dosse and Amblyseius hibisci Chant (Acarina: Phytoseiidae) on various kinds of food substances. Entomophaga, 15, 93-106. https://doi.org/10.1007/bf02371627
Tanigoshi, L. K. (1982). Advances in knowledge of the biology of the Phytoseiidae. 1-22. In: U. Gerson, R. L. Smiley & R. Ochoa. Mites (acari) for Pest Control. Blackwell Science Ltd.
Timms, J. E., Oliver, T. H., Straw, N. A., & Leather, S. R. (2008). The effects of host plant on three coccinellid functional response. Is the conifer specialist Aphidecta obliterate (L.) (Coleoptera: coccinelidae) better adapted to spruce than the generalist Adatia bipunctat (L.) (Coloptera: Coccinelidae)? Biological Control, 47, 273-281. https://doi.org/10.1016/j.biocontrol.2008.08.009.
Reis, P. R., Teodoro, A. V., Eto, M. V., & Silva, E. V. (2007). Life history of Amblyseius herbicolus (Chant) (Acari: Phytoseiidae) on coffee plants. Neotropical Entomology, 36, 282-287. https://doi.org/10.1590/s1519-566x2007000200016
Van Alphen, J. J. M., & Jervis, M. A, (1996). Foraging behaviour. In: M. Jervis & N. Kidd (Eds). Insect Natural Enemies Practical Approaches to Their Study and Evaluation. Chapman & Hall.London, 491 p.
van Lenteren, J. C., & De Ponti, O. M. B. (1990). Plant- leaf morphology, host- plant resistance and biological control. Symposia biologica hungarica. Hungary, 39, 365-386.
van Rijn, P. C. I., & Tanigoshi, L. K. (1999). Pollen as food for the predatory mites Iphiseius degenerans and Neoseiulus cucumeris (Acari: Phytoseiidae): dietary range and life history. Experimental Applied Acarology, 23, 785-805. https://doi.org/10.1023/A:1006227704122
Vacacela, H. E., Colares, E., Lemos, F., Marques, P. H., Franlin, E. C. (2019). Supplementary food for Neoseiulus californicus boosts biological control of Tetranychus urticae on strawberry. Pest Manag Science, 75(7), 1989-1992. https://doi.org/10.1002/ps.5312
Walzer, A., Castagnoli, M., Simoni, S., & Liguori, M. (2007). Intraspecifc variation in humidity susceptibility of the predatory mite Neoseiulus californicus: Survival, development and reproduction. Biological Control, 41, 42-52. https://doi.org/10.1016/j.biocontrol.2006.11.012
Weintraub, P., & Palevsky, E. (2008). Evaluation of the predatory mite, Neoseiulus californicus,f or spider mite control on greenhouse sweet pepper under hot arid weld conditions. Experimental Applied Acarology, 45, 29-37. https://doi.org/10.1007/s10493-008-9169-3
Xiao, Y., & Fadamiro, H. Y. (2010). Functional responses and prey-stage preferences of three species of predacious mites (Acari: Phytoseiidae) on citrus red mite, Panonychus citri (Acari: Tetranychidae). Biogical Control, 53, 345-352. https://doi.org/10.1016/j.biocontrol.2010.03.001
Yan, L., Mori, Sh., Haroyama, N., HiraL, N., & Osakable, M. (2020). Strawberry pollen as a source of UV‐B protection ingredients for the phytoseiid mite Neoseiulus californicus (Acari: Phytoseiidae). Pest Management Science77(2). https://doi.org/10.1002/ps.6089
 
Yue, B., & Tsai, J. H. (1996). Development, survivorship and reproduction of Amblyseius largoensis (Acari: Phytoseiidae) on selected plant pollens and temperatures. Environmental of Entomology, 125, 488- 494. https://doi.org/10.1093/ee/25.2.488
Zhang, B. X., Li, D. S., Feng, L., & Huang, S. H. (2007). Research progress of mass production and release technologies of predatory mites. Chinese Journal of Biological Control, 23, 279-283.
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