Abstract
The phytoseiid Proprioseiopsis mexicanus has been collected from a wide range of plants in the western hemisphere, including many cucurbit agroecosystems in South Carolina, USA. Our aim was to characterize the lifestyle of P. mexicanus and its potential as a natural enemy of Tetranychus urticae, a common pest in cucurbits. We determined developmental time, pre-oviposition time, and fecundity of females on pollen-only diets from a commercial Typha spp. supplement source, Citrullus lanatus, Cucurbita maxima, Cucurbita moschata, Cucurbita pepo, Delosperma cooperi, Trifolium incarnatum, and on T. urticae and a combination of T. urticae and Typha spp. pollen. Female development time differed based on diet—development was fastest on C. lanatus and D. cooperi diets (ca. 3 days) and slowest on Typha pollen diet (ca. 5 days). Pre-oviposition time was shorter for females fed C. lanatus and T. incarnatum (1.6 days) and longest when fed Typha pollen (3.1 days). Citrullus lanatus, T. incarnatum, and D. cooperi pollen diets resulted in more eggs/day compared to other diets. Cucurbita moschata pollen resulted in the lowest oviposition rate (0.69 eggs/day). Because these pollens varied in size, we examined pollen size as a factor in developmental and reproductive success. With the exception of Typha pollen, small-pollen diets (C. lanatus, D. cooperi, and T. incarnatum) resulted in faster development, shorter pre-oviposition time, and higher fecundity than large-pollen diets (Cucurbita spp.). We concluded that P. mexicanus is a generalist predator that may require pollen for survival and reproduction, but alone this species may not be an effective predator of T. urticae.
Similar content being viewed by others
Data availability
Datasets are available at figshare.com.
Code availability
R Statistical Software packages ggplot2, multcomp, and cluster.
References
Abou-Setta MM, Childers CC (1989) Biology of Euseius mesembrinus (Acari: Phytoseiidae): life tables and Feeding behavior on tetranychid mites on citrus. Environ Entomol 18:665–669. https://doi.org/10.1093/ee/18.4.665
Abou-Setta MM, Fouly AH, Childers CC (1997) Biology of Proprioseiopsis rotendus (Acari: Phytoseiidae) reared on Tetranychus urticae (Acari: Tetranychidae) or pollen. Fla Entomol 50:27–34. https://doi.org/10.2307/3495973
Badii M, McMurtry J (1983) Effect of different foods on development, reproduction and survival of Phytoseiulus longipes [Acarina: Phytoseiidae]. Entomophaga 28:161–166. https://doi.org/10.1007/BF02372140
Ball JC (1980) Development, fecundity, and prey consumption of four species of predacious mites (Phytoseiidae) at two constant temperatures. Environ Entomol 9:298–303. https://doi.org/10.1093/ee/9.3.298
Blackwood JS, Luh H-K, Croft BA (2004) Evaluation of prey-stage preference as an indicator of life-style type in phytoseiid mites. Exp Appl Acarol 33:261–280. https://doi.org/10.1023/B:APPA.0000038623.75416.e3
Blackwood JS, Schausberger P, Croft BA (2001) Prey-stage preference in generalist and specialist phytoseiid mites (Acari: Phytoseiidae) when offered Tetranychus urticae (Acari: Tetranychus) eggs and larvae. Environ Entomol 30:1103–1111. https://doi.org/10.1603/0046-225X-30.6.1103
Calvo F, Bolckmans K, Belda J (2011) Control of Bemisia tabaci and Frankliniella occidentalis in cucumber by Amblyseius swirskii. Biocontrol 56:185–192. https://doi.org/10.1007/s10526-010-9319-5
Croft B, Blackwood J, McMurtry J (2004) Classifying life-style types of phytoseiid mites: diagnostic traits. Exp Appl Acarol 33:247–260. https://doi.org/10.1023/B:APPA.0000038622.26584.82
Denmark HA, Evans GA (2011) Phytoseiidae of North America and Hawaii:(Acari, Mesostigmata). Indira Publishing House, West Bloomfield, MI, USA
Fadamiro HY, Xiao Y, Nesbitt M, Childers CC (2009) Diversity and seasonal abundance of predacious mites in Alabama Satsuma citrus. Ann Entomol Soc Am 102:617–628. https://doi.org/10.1603/008.102.0406
Ferguson G (2008) Combined use of predatory mites for biological control of Tetranychus urticae (Acari: Tetranychidae) in commercial greenhouse cucumber. IOBC WPRS Bulletin 32:59
Finkelstein SA (2003) Identifying pollen grains of Typha latifolia, Typha angustifolia, and Typha×glauca. Can J Bot 81:985–990. https://doi.org/10.1139/b03-084
Fouly AH, Abou-Setta MM, Childers CC (1995) Effects of diet on the biology and life tables of Typhlodromalus peregrinus (Acari: Phytoseiidae). Environ Entomol 24:870–874. https://doi.org/10.1093/ee/24.4.870
Gillespie DR (1989) Biological control of thrips [Thysanoptera: Thripidae] on greenhouse cucumber by Amblyseius cucumeris. Entomophaga 34:185–192. https://doi.org/10.1007/bf02372667
Goleva I, Zebitz CPW (2013) Suitability of different pollen as alternative food for the predatory mite Amblyseius swirskii (Acari, Phytoseiidae). Exp Appl Acarol 61:259–283. https://doi.org/10.1007/s10493-013-9700-z
Horsburgh RL, Asquith D (1968) Initial survey of arthropod predators of the European red mite in south-central Pennsylvania. J Econ Entomol 61:1752–1754. https://doi.org/10.1093/jee/61.6.1752
Hothorn T, Bretz F, Westfall P (2008) Simultaneous inference in general parametric models. Biom J 50:346–363. https://doi.org/10.1002/bimj.200810425
Kakkar G, Kumar V, Seal DR, Liburd OE, Stansly PA (2016) Predation by Neoseiulus cucumeris and Amblyseius swirskii on Thrips palmi and Frankliniella schultzei on cucumber. Biol Control 92:85–91. https://doi.org/10.1016/j.biocontrol.2015.10.004
Knisley CB, Denmark HA (1978) New phytoseiid mites from successional and climax plant communities in New Jersey. Fla Entomol 61:5–17. https://doi.org/10.2307/3494423
Maechler M, Rousseeuw P, Struyf A, Hubert M, Hornik K (2019) Cluster: cluster analysis basics and extensions. 2.1.0 edn.
Martin PS, Drew CM (1969) Scanning electron photomicrographs of Southwestern pollen grains. J Arizona-Nevada Acad Sci 5:147–176. https://doi.org/10.2307/40022035
McMurtry JA (1977) Some predaceous mites (Phytoseiidae) on citrus in the mediterranean region. Entomophaga 22:19–30. https://doi.org/10.1007/BF02372986
McMurtry JA (1981) The use of phytoseiids for biological control: progress and future prospects. In: Hoy MA (ed) Formal Conference of the Acarological Society of America, San Diego, pp 23–48
McMurtry JA (1992) Dynamics and potential impact of ‘generalist’ phytoseiids in agroecosystems and possibilities for establishment of exotic species. Exp Appl Acarol 14:371–382. https://doi.org/10.1007/BF01200574
McMurtry JA, Croft B (1997) Life-styles of phytoseiid mites and their roles in biological control. Annu Rev Entomol 42:291–321. https://doi.org/10.1146/annurev.ento.42.1.291
McMurtry JA, Rodriguez J (1987) Nutritional ecology of phytoseiid mites Nutritional ecology of insects, mites and spiders. Wiley, New York
McMurtry JA, De Moraes GJ, Sourassou NF (2013) Revision of the lifestyles of phytoseiid mites (Acari: Phytoseiidae) and implications for biological control strategies. Syst Appl Acarol 18:297–320. https://doi.org/10.11158/saa.18.4.1
Messelink GJ, van Steenpaal S, van Wensveen W (2005) Typhlodromips swirskii (Athias-Henriot)(Acari: Phytoseiidae): a new predator for thrips control in greenhouse cucumber. IOBC WPRS Bulletin 28:183–186
Messelink GJ, Van Steenpaal SEF, Ramakers PMJ (2006) Evaluation of phytoseiid predators for control of western flower thrips on greenhouse cucumber. Biol Control 51:753–768. https://doi.org/10.1007/s10526-006-9013-9
Messelink GJ, Van Maanen R, Van Holstein-Saj R, Sabelis MW, Janssen A (2010) Pest species diversity enhances control of spider mites and whiteflies by a generalist phytoseiid predator. Biocontrol 55:387–398. https://doi.org/10.1007/s10526-009-9258-1
Nguyen DT, Than AT, Jonckheere W, Nguyen VH, Van Leeuwen T, De Clercq P (2019) Life tables and feeding habits of Proprioseiopsis lenis (Acari: Phytoseiidae) and implications for its biological control potential in Southeast Asia. Syst Appl Acarol 24:857–865. https://doi.org/10.11158/saa.24.5.9
Nomikou M, Janssen A, Schraag R, Sabelis MW (2002) Phytoseiid predators suppress populations of Bemisia tabaci on cucumber plants with alternative food. Exp Appl Acarol 27:57. https://doi.org/10.1023/A:1021559421344
Nomikou M, Sabelis MW, Janssen A (2010) Pollen subsidies promote whitefly control through the numerical response of predatory mites. Biol Control 55:253–260. https://doi.org/10.1007/s10526-009-9233-x
Putman WL (1962) Life-history and behaviour of the predacious mite Typhlodromus (T.) caudiglans Schuster (Acarina: Phytoseiidae) in Ontario, with notes on the prey of related species. Can Entomol 94:163–177. https://doi.org/10.4039/Ent94163-2
R Core Team (2019) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria
Rezende JM, Lofego AC (2012) Mites (Mesostigmata, Prostigmata, Astigmatina) associated with weeds among physic nut crops (Jatropha curcas L.: Euphorbiaceae) in Brazil. Syst Appl Acarol 17:15–26. https://doi.org/10.11158/saa.17.1.5
Rezende JM, Verona RLC, Lofego AC (2016) Mites (Acari) inhabiting Jatropha curcas L. (Euphorbiaceae) crops: the role of seasonality and weeds. Syst Appl Acarol 21:1515–1524. https://doi.org/10.11158/saa.21.11.7
Schmidt-Jeffris RA, Beers EH (2015) Comparative biology and pesticide susceptibility of Amblydromella caudiglans and Galendromus occidentalis as spider mite predators in apple orchards. Exp Appl Acarol 67:35–47. https://doi.org/10.1007/s10493-015-9931-2
Stansly PA, Castillo J (2009) Control of broad mite, Polyphagotarsonemus latus and the whitefly Bemisia tabaci in open field pepper and eggplant with predaceous mites. Paper presented at the Proceedings of the IOBC WPRS Working Group ‘Integrated Control in Protected Crops’, Crete, Greece, 9–11 September 2009
Trottin-Caudal Y, Leyre J, Baffert V, Fournier C, Chabriere C (2008) Experimental studies on Typhlodromips (Amblyseius) swirskii in greenhouse cucumbers. IOBC WPRS Bulletin 32:213
van Rijn PC, Sabelis MW (1990) Pollen as an alternative food source for predatory mites and its effect on the biological control of thrips in greenhouses. Proc Exp Appl Entomol 1:44–48
van Rijn PC, Tanigoshi LK (1999) Pollen as food for the predatory mites Iphiseius degenans and Neoseiulus cucumeris (Acari: Phytoseiidae): dietary range and life history. Exp Appl Acarol 23:785–802. https://doi.org/10.1023/A:1006227704122
Wäckers F, Put K, Bollens T (2015) Pollen composition and uses thereof. Belgium Patent WO 2015/124704, 27 August 2015
Warburg S, Inbar M, Gal S, Salomon M, Palevsky E, Sadeh A (2019) The effects of a windborne pollen-provisioning cover crop on the phytoseiid community in citrus orchards in Israel. Pest Manag Sci 75:405–412. https://doi.org/10.1002/ps.5129
Wickham H (2016) ggplot2: elegant graphics for data analysis. Springer-Verlag, New York
Wu S, Gao Y, Xu X, Wang E, Wang Y, Zhongren L (2014) Evaluation of Stratiolaelaos scimitus and Neoseiulus barkeri for biological control of thrips on greenhouse cucumbers. Biocontrol Sci Technol 24:1110–1121. https://doi.org/10.1080/09583157.2014.924478
Acknowledgements
We thank Amnon Levi (USDA Vegetable Laboratory, Charleston, SC) for providing Citrullus lanatus pollen for this experiment. We thank the lab of Anthony Keinath for the use of equipment in our pollen diameter measurements. This work was supported by the NIFA Postdoctoral Fellowship grant no. 2018-67012-27994/Project accession no. 1015537 from the USDA National Institute of Food and Agriculture. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture. USDA is an equal opportunity provider and employer.
Funding
This work was supported by the NIFA Postdoctoral Fellowship grant no. 2018–67012-27994/Project accession no. 1015537 from the USDA National Institute of Food and Agriculture.
Author information
Authors and Affiliations
Contributions
All authors contributed to the study concept and design. Material preparation and data collection were performed by MAF and JC. Data analysis was performed by MAF. The first draft of the manuscript was written by MAF and all authors commented on the previous versions of the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Conflicts of interest
All authors have no relevant financial or non-financial interests to disclose.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Farfan, M.A., Coffey, J. & Schmidt-Jeffris, R.A. Suitability of food resources for Proprioseiopsis mexicanus, a potentially important natural enemy in eastern USA agroecosystems. Exp Appl Acarol 84, 121–134 (2021). https://doi.org/10.1007/s10493-021-00622-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10493-021-00622-6