Hostname: page-component-8448b6f56d-qsmjn Total loading time: 0 Render date: 2024-04-23T07:30:15.579Z Has data issue: false hasContentIssue false
  • English
  • Français

Supplementation of natural prey with pollen grains exerts an influence on the life table parameters of Neoseiulus californicus

Published online by Cambridge University Press:  09 March 2020

Afsaneh Soltaniyan ,
Katayoon Kheradmand Open the ORCID record for Katayoon Kheradmand [Opens in a new window] ,
Yaghoub Fathipour Open the ORCID record for Yaghoub Fathipour [Opens in a new window]  and
Davoud Shirdel
Afsaneh Soltaniyan
Affiliation:
Department of Entomology and Plant Pathology, College of Aburaihan, University of Tehran, Pakdasht, Iran
Katayoon Kheradmand*
Affiliation:
Department of Entomology and Plant Pathology, College of Aburaihan, University of Tehran, Pakdasht, Iran
Yaghoub Fathipour
Affiliation:
Department of Entomology, Faculty of Agriculture, Tarbiat Modares University, P.O. Box 14115-336, Tehran, Iran
Davoud Shirdel
Affiliation:
Plant Protection Research Department, East Azarbaijan Agricultural and Natural Resources Research Center, AREEO, Tabriz, Iran
*
Author for correspondence: Katayoon Kheradmand, Email: kkheradmand@ut.ac.ir
Get access Rights & Permissions [Opens in a new window]

Abstract

Better performance of generalist predators, as well as an increase in their density, may be an incentive factor in the ability of the predators to exploit more than one food item or mixed diets. In this study, the effects of four pollen grains (cedar, pear, apricot, and pistachio) when provided to Neoseiulus californicus in mixed diets with prey, Tetranychus urticae, were evaluated. The result indicated that the fastest female developmental time was observed on pistachio pollen + T. urticae, together with apricot pollen + T. urticae. Females reared on the mixed diet comprising pistachio pollen reflected the longest total life span duration, while the shortest total life span was observed in those on the diet that included pear pollen. Furthermore, the lowest fecundity, as well as the shortest reproduction period, was determined on the diets that included pear pollen, while the highest fecundity and the longest reproduction period were observed in pistachio pollen + T. urticae. In addition, the intrinsic (r) and finite rate of increase (λ), net (R0) and gross (GRR) reproductive rates were highest in pistachio pollen + T. urticae. These findings have important implications for developing a comprehensive biological control program of T. urticae, which will be discussed.

Keywords

Biological controlmixed dietNeoseiulus californicuspollenTetranychus urticae
Type
Research Paper
Information
Bulletin of Entomological Research , Volume 110 , Issue 4 , August 2020 , pp. 535 - 541
Check for updates
Copyright
Copyright © Cambridge University Press 2020

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

Akkopru, EP, Atlihan, R, Okut, H and Chi, H (2015) Demographic assessment of plant cultivar resistance to insect pests: a case study of the dusky-veined walnut aphid (Hemiptera: Callaphididae) on five walnut cultivars. Journal of Economic Entomology 108, 378–387.CrossRefGoogle ScholarPubMed
Barber, A, Campbell, CAM, Crane, H, Lilley, R and Tregidga, E (2003) Biocontrol of two-spotted spider mite Tetranychus urticae on dwarf hops by the phytoseiid mites Phytoseiulus persimilis and Neoseiulus californicus. Biocontrol Science and Technology 13, 275–284.CrossRefGoogle Scholar
Buitenhuis, R, Murphy, G, Shipp, L and Scott-Dupree, C (2015) Amblyseius swirskii in greenhouse production systems: a floricultural perspective. Experimental & Applied Acarology 65, 451–464.CrossRefGoogle ScholarPubMed
Chi, H (1988) Life-table analysis incorporating both sexes and variable development rates among individuals. Environmental Entomology 17, 26–34.CrossRefGoogle Scholar
Chi, H (2016) TWOSEX-MSChart: a computer program for the age-stage, two-sex life table analysis. Available at http://140.120.197.173/Ecology/Download/TWOSEX-MSChart.rar (Accessed February 2016).Google Scholar
Chi, H and Liu, H (1985) Two new methods for the study of insect population ecology. Bulletin of the Institute of Zoology Academia Sinica 24, 225–240.Google Scholar
Duso, C, Pozzebon, A, Capuzzo, C, Bisol, PM and 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, 229–241.CrossRefGoogle Scholar
El Taj, DF and Chuleui, J (2012) Effect of temperature on the life-history traits of Neoseiulus californicus (Acari: Phytoseiidae) fed on Panonychus ulmi. Experimental and Applied Acarology 56, 247–260.CrossRefGoogle ScholarPubMed
Hoogerbrugge, H, van Houten, YM, Knapp, M and Bolckmans, K (2011) Biological control of thrips and whitefly on strawberries with Amblydromalus limonicus and Amblyseius swirskii. IOBC/WPRS Bull 68, 65–69.Google Scholar
Huang, YB and Chi, H (2012) Assessing the application of the jackknife and bootstrap techniques to the estimation of the variability of the net reproductive rate and gross reproductive rate: a case study in Bactrocera cucurbitae (Coquillett) (Diptera: Tephritidae). Journal of Agriculture & Forest Entomology 61, 37–45.Google Scholar
Khanamani, M, Fathipour, Y, Talebi, AA and Mehrabadi, M (2017a) Linking pollen quality and performance of Neoseiulus californicus (Acari: Phytoseiidae) in two-spotted spider mite management programmes. Pest Management Science 73, 452–461.CrossRefGoogle Scholar
Khanamani, M, Fathipour, Y, Talebi, AA and Mehrabadi, M (2017b) How pollen supplementary diet affect life table and predation capacity of Neoseiulus californicus on two-spotted spider mite. Systematic and Applied Acarology 22, 135–147.CrossRefGoogle Scholar
Khanamani, M, Fathipour, Y, Talebi, AA and Mehrabadi, M (2017c) Evaluation of different artificial diets for rearing the predatory mite Neoseiulus californicus (Acari: Phytoseiidae): diet-dependent life table studies. Acarologia 57, 407–419.CrossRefGoogle Scholar
McMurtry, JA and Croft, BA (1997) Life-style of phytoseiid mites and their role in biological control. Annual Review of Entomology 42, 291–321.CrossRefGoogle Scholar
McMurtry, JA, De Moraes, GJ and Sourassou, NF (2013) Revision of the lifestyles of phytoseiid mites (Acari: Phytoseiidae). Systematic and Applied Acarology 18, 297–320.CrossRefGoogle Scholar
Momen, F and El-Borolossy, M (2010) Juvenile survival and development in three phytoseiid species (Acari: Phytoseiidae) feeding on con- and heterospecific immatures. Acta Phytopathologica et Entomologica Hungarica 45, 349–357.CrossRefGoogle Scholar
Nomikou, M, Janssen, A, Schraag, R and Sabelis, MW (2002) Phytoseiid predators suppress populations of Bemisia tabaci on cucumber plants with alternative food. Experimental and Applied Acarology 27, 57–68.CrossRefGoogle ScholarPubMed
Nomikou, M, Janssen, A and Sabelis, MW (2003) Phytoseiid predators of whiteflies feed and reproduce on non-prey food sources. Experimental and Applied Acarology 31, 15–26.CrossRefGoogle ScholarPubMed
Nomikou, M, Sabelis, MW and Janssen, A (2010) Pollen subsidies promote whitefly control through the numerical response of predatory mites. BioControl 55, 253–260.CrossRefGoogle Scholar
Nguyen, DT, Bouguet, V, Spranghers, T, Vangansbeke, D and De Clercq, P (2015) Beneficial effect of supplementing an artificial diet for Amblyseius swirskii with Hermetia illucens haemolymph. Journal of Applied Entomology 139, 342–351.CrossRefGoogle Scholar
Pappas, ML, Xanthis, C, Samaras, K, Koveos, DS and Broufas, GD (2013) Potential of the predatory mite Phytoseius finitimus (Acari: Phytoseiidae) to feed and reproduce on greenhouse pests. Experimental and Applied Acarology 61, 387–401.CrossRefGoogle ScholarPubMed
Rahmani, H, Fathipour, Y and Kamali, K (2009) Life history and population growth parameters of Neoseiulus californicus (Acari: Phytoseiidae) fed on Thrips tabaci (Thysanoptera: Thripidae) in laboratory conditions. Systematic and Applied Acarology 14, 91–100.CrossRefGoogle Scholar
Riahi, E, Fathipour, Y, Talebi, AA and 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, 1399–1412.CrossRefGoogle Scholar
Riahi, E, Fathipour, Y, Talebi, AA and Mehrabadi, M (2017a) 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, 244–253.Google Scholar
Riahi, E, Fathipour, Y, Talebi, AA and Mehrabadi, M (2017b) Natural diets versus factitious prey: comparative effects on development, fecundity and life table of Amblyseius swirskii (Acari: Phytoseiidae). Systematic and Applied Acarology 22, 711–723.CrossRefGoogle Scholar
Riahi, E, Fathipour, Y, Talebi, AA and Mehrabadi, M (2017c) Attempt to develop cost-effective rearing of Amblyseius swirskii (Acari: Phytoseiidae): assessment of different artificial diets. Journal of Economic Entomology 110, 1525–1532.CrossRefGoogle Scholar
van Rijn, PCJ and Tanigoshi, LK (1999) Pollen as food for the predatory mites Iphiseius degenerans and Neoseiulus cucumeris (Acari: Phytoseiidae): dietary range and life history. Experimental and Applied Acarology 23, 785–202.CrossRefGoogle Scholar
Van Rijn, PCJ, Van Houten, YM and Sabelis, MW (1999) Pollen improves thrips control with predatory mites. IOBC/WPRS Bull 22, 209–212.Google Scholar
van Rijn, PCJ, Van Houten, YM and Sabelis, MW (2002) How plants benefit from providing food to predators even when it is also edible to herbivores. Ecology 83, 2664–2679.CrossRefGoogle Scholar
Zemek, R and Prenerova, E (1997) Powdery mildew (Ascomycotina: Erysiphales) an alternative food for the predatory mite Typhlodromus pyri Scheuten (Acari: Phytoseiidae). Experimental and Applied Acarology 21, 405–414.CrossRefGoogle Scholar