Hostname: page-component-cd9895bd7-gvvz8 Total loading time: 0 Render date: 2024-12-23T23:58:04.406Z Has data issue: false hasContentIssue false

The efficiency of Amblyseius swirskii in control of Tetranychus urticae and Trialeurodes vaporariorum is affected by various factors

Published online by Cambridge University Press:  30 August 2018

N. Mortazavi
Affiliation:
Department of Entomology, Faculty of Agriculture, Tarbiat Modares University, P.O. Box 14115-336, Tehran, Iran
Y. Fathipour*
Affiliation:
Department of Entomology, Faculty of Agriculture, Tarbiat Modares University, P.O. Box 14115-336, Tehran, Iran
A.A. Talebi
Affiliation:
Department of Entomology, Faculty of Agriculture, Tarbiat Modares University, P.O. Box 14115-336, Tehran, Iran
*
*Author for correspondence Phone: +98 21 48292301 Fax: +98 21 48292200 E-mail: [email protected]

Abstract

Amblyseius swirskii Athias-Henriot is a well-known predator that is used for controlling the population of two-spotted spider mites (TSSM), Tetranychus urticae Koch, and greenhouse whitefly (GHWF), Trialeurodes vaporariorum Westwood, in strawberry greenhouses. To find the effective factors that influence the efficiency of this predator, the predation rates of A. swirskii fed on (Ι) TSSM in the presence and absence of the pollen, webbing, and GHWF, as well as on (II) GHWF in the presence and absence of the pollen, and GHWF-produced honeydew were determined. Furthermore, developmental time, fecundity, and population growth rate of this predator under the same conditions were measured. Our results showed that A. swirskii was able to reduce TSSM population, while the spider mite webbing had an adverse effect on the performance of the predator. Therefore, the presence of the predator population at the time of the infestation is crucial to the success of biological control. It can be concluded that the alternative food sources such as pollen and GHWF-produced honeydew play an important role in maintaining the predator population in the absence of pests. Moreover, the results indicate that using the pollen and another pest along with the target pest can promote the predator density. A. swirskii consumed lower numbers of TSSM when concurrently offered with GHWF and/or maize pollen, and lower numbers of GHWF in the presence of pollen. On the other hand, in the presence of alternative food or alternative prey, the fecundity of the predator was much higher.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2018 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bostanian, N.J., Beudjekian, S., McGregor, E. & Racette, G. (2009) A modified excised leaf disc method to estimate the toxicity of slow-and fast-acting reduced-risk acaricides to mites. Journal of Economic Entomology 102, 20842089.10.1603/029.102.0610Google Scholar
Buitenhuis, R., Murphy, G., Shipp, L. & Scott-Dupree, C. (2015) Amblyseius swirskii in greenhouse production systems: a floricultural perspective. Experimental and Applied Acarology 65, 451464.10.1007/s10493-014-9869-9Google Scholar
Calvo, F.J., Knapp, M., van Houten, Y.M., Hoogerbrugge, H. & Belda, J.E. (2015) Amblyseius swirskii: what made this predatory mite such a successful biocontrol agent? Experimental and Applied Acarology 65, 419433.Google Scholar
Chi, H. (1988) Life-table analysis incorporating both sexes and variable development rates among individuals. Environmental Entomology 17, 2634.10.1093/ee/17.1.26Google Scholar
Chi, H. (2016 a) TWOSEX-MS Chart: a computer program for the age-stage, two-sex life table analysis. Available online at http://140.120.197.173/Ecology/Download/TWOSEX-MSChart.rar (accessed February 2016).Google Scholar
Chi, H. (2016 b) CONSUME-MSChart: Computer program for consumption rate analysis based on the age stage, two-sex life table. Available online at http://140.120.197.173/Ecology/Download/CONSUMSChart.rar (accessed February 2016).Google Scholar
Chi, H. & Liu, H. (1985) Two new methods for the study of insect population ecology. Bulletin of the Institute of Zoology, Academia Sinica 24, 225240.Google Scholar
Chi, H. & Yang, T.-C. (2003) Two-sex life table and predation rate of Propylaea japonica Thunberg (Coleoptera: Coccinellidae) fed on Myzus persicae (Sulzer)(Homoptera: Aphididae). Environmental Entomology 32, 327333.10.1603/0046-225X-32.2.327Google Scholar
Delisle, J., Brodeur, J. & Shipp, L. (2015) Evaluation of various types of supplemental food for two species of predatory mites, Amblyseius swirskii and Neoseiulus cucumeris (Acari: Phytoseiidae). Experimental and Applied Acarology 65, 483494.10.1007/s10493-014-9862-3Google Scholar
Duso, C., Pozzebon, A., Capuzzo, C., Bisol, P.M. & Otto, S. (2003) Grape downy mildew spread and mite seasonal abundance in vineyards: evidence for the predatory mites Amblyseius andersoni and Typhlodromus pyri. Biological Control 27, 229241.10.1016/S1049-9644(03)00016-1Google Scholar
Fathipour, Y. & Maleknia, B. (2016) Mite predators. pp. 329366 in Omkar, (Ed.) Ecofriendly Pest Management for Food Security. San Diego, USA, Elsevier.10.1016/B978-0-12-803265-7.00011-7Google Scholar
Gould, H. (1977) Biological control of glasshouse whitefly and red spider mite on tomatoes and cucumbers in England and Wales, 1975–76. Plant Pathology 26, 5760.10.1111/j.1365-3059.1977.tb01023.xGoogle Scholar
Holt, R.a. & Lawton, J. (1994) The ecological consequences of shared natural enemies. Annual Review of Ecology, Evolution, and Systematics 25, 495520.Google Scholar
Janssen, A. & Sabelis, M.W. (2015) Alternative food and biological control by generalist predatory mites: the case of Amblyseius swirskii. Experimental and Applied Acarology 65, 413418.10.1007/s10493-015-9901-8Google Scholar
Juan-Blasco, M., Qureshi, J.A., Urbaneja, A. & Stansly, P.A. (2012) Predatory mite, Amblyseius swirskii (Acari: Phytoseiidae), for biological control of Asian citrus psyllid, Diaphorina citri (Hemiptera: Psyllidae). Florida Entomologist 95, 543551.Google Scholar
Khanamani, M., Fathipour, Y. & Hajiqanbar, H. (2013) Population growth response of Tetranychus urticae to eggplant quality: application of female age-specific and age-stage, two-sex life tables. International Journal of Acarology 39, 638648.Google Scholar
Khanamani, M., Fathipour, Y., Talebi, A.A. & Mehrabadi, M. (2017) Quantitative analysis of long-term mass rearing of Neoseiulus californicus (Acari: Phytoseiidae) on almond pollen. Journal of Economic Entomology 110, 14421450.Google Scholar
Lemos, F., Sarmento, R.A., Pallini, A., Dias, C.R., Sabelis, M.W. & Janssen, A. (2010) Spider mite web mediates anti-predator behaviour. Experimental and Applied Acarology 52, 110.10.1007/s10493-010-9344-1Google Scholar
Messelink, G.J. & Janssen, A. (2009) Whitefly-induced plant defenses in cucumber and their impact on biological control of spider mites. IOBC/wprs Bulletin 50, 6363.Google Scholar
Messelink, G.J., van Maanen, R., van Steenpaal, S.E. & Janssen, A. (2008) Biological control of thrips and whiteflies by a shared predator: two pests are better than one. Biological Control 44, 372379.10.1016/j.biocontrol.2007.10.017Google Scholar
Messelink, G.J., Van Maanen, R., Van Holstein-Saj, R., Sabelis, M.W. & Janssen, A. (2010) Pest species diversity enhances control of spider mites and whiteflies by a generalist phytoseiid predator. Biocontrol 55, 387398.10.1007/s10526-009-9258-1Google Scholar
Mortazavi, N., Fathipour, Y. & Talebi, A.A. (2017) Interactions between two-spotted spider mite, Tetranychus urticae and greenhouse whitefly, Trialeurodes vaporariorum on strawberry. Systematic and Applied Acarology 22, 20832092.10.11158/saa.22.12.5Google Scholar
Nomikou, M., Janssen, A. & Sabelis, M.W. (2003) Phytoseiid predators of whiteflies feed and reproduce on non-prey food sources. Experimental and Applied Acarology 31, 1526.Google Scholar
Nomikou, M., Janssen, A. & Sabelis, M.W. (2010) Pollen subsidies promote whitefly control through the numerical response of predatory mites. Biocontrol 55, 253260.Google Scholar
Ragusa, S. & Swirski, E. (1977) Feeding habits, post-embryonic and adult survival, mating, virility and fecundity of the predacious mite Amblyseius swirskii [Acarina: Phytoseiidae] on some coccids and mealybugs. Biocontrol 22, 383392.Google Scholar
Rezaie, M., Saboori, A., Baniamerie, V. & Allahyari, H. (2013) Susceptibility of Tetranychus uticae Koch (Acari: Tetranychidae) on seven strawberry cultivars. International Research Journal of Applied and Basic Sciences 4, 24552463.Google Scholar
Riahi, E., Fathipour, Y., Talebi, A.A. & Mehrabadi, M. (2016) Pollen quality and predator viability: life table of Typhlodromus bagdasarjani on seven different plant pollens and two-spotted spider mite. Systematic and Applied Acarology 21, 13991412.Google Scholar
Riahi, E., Fathipour, Y., Talebi, A.A. & Mehrabadi, M. (2017) Linking life table and consumption rate of Amblyseius swirskii (Acari: Phytoseiidae) in presence and absence of different pollens. Annals of the Entomological Society of America 110, 244253.Google Scholar
Sabelis, M.W. & Bakker, F.M. (1992) How predatory mites cope with the web of their tetranychid prey: a functional view on dorsal chaetotaxy in the Phytoseiidae. Experimental & Applied Acarology 16, 203225.10.1007/BF01193804Google Scholar
Swirski, E. (1967) Laboratory studies on the feeding, development and reproduction of the predaceous mites Amblyseius rubini swirski and Amitai and Amblyseius swirski Athias (Acarina: Phytoseiidae) on various kinds of food substances. Israel Journal of Agricultural Research 17, 101119.Google Scholar
Van Lenteren, J., Babendreier, D., Bigler, F., Burgio, G., Hokkanen, H., Kuske, S., Loomans, A., Menzler-Hokkanen, I., Van Rijn, P. & Thomas, M. (2003) Environmental risk assessment of exotic natural enemies used in inundative biological control. BioControl 48, 338.Google Scholar
Weis, J.S., Smith, G. & Santiago-Bass, C. (2000) Predator/prey interactions: a link between the individual level and both higher and lower level effects of toxicants in aquatic ecosystems. Journal of Aquatic Ecosystem Stress and Recovery 7, 145153.Google Scholar