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Issue: Vol. 22: 30 Nov. 2022
Type: Proceedings Papers
Published: 2022-11-30
DOI: 10.11646/zoosymposia.22.1.72
Page range: 117–120
Abstract views: 149
PDF downloaded: 14

Dosage-dependent and prey stage-specific non-consumptive effects of predators on prey: interactions between Neoseiulus cucumeris and Tyrophagus putrescentiae

School of Biological Sciences, The University of Auckland, Auckland, New Zealand
School of Biological Sciences, The University of Auckland, Auckland, New Zealand, Manaaki Whenua Landcare Research, Auckland, New Zealand, 1072
Neoseiulus cucumeris Tyrophagus putrescentiae

Abstract

Predators can affect prey both directly through consumption and indirectly through non-consumptive effects such as predation risk. The latter has been less studied than consumptive effects in predator-prey interactions, although many studies have shown that non-consumptive effects could significantly affect various life history traits of the prey (Clinchy et al. 2013; Gurr et al. 2017; Hawlena & Schmitz 2010; Hermann & Thaler 2014; McCauley et al. 2011; Peckarsky et al. 2002; Skelhorn et al. 2011; Stoks 2001; Zanette et al. 2011), such as development, reproduction and lifespan in mite prey-predator systems (Choh & Takabayashi 2010; Freinschlag & Schausberger 2016; Grostal & Dicke 1999; Li & Zhang 2019; Ristyadi et al. 2022; Škaloudová et al. 2007; Wei & Zhang 2019, 2022). Most published studies examined the short-term effects of predation risk on prey immature development, reproduction and behaviour (e.g. Abrams & Rowe 1996; Choh et al. 2010; Majchrzak et al. 2022; Oku et al. 2003; Oliveira & Moraes 2021; Rocha et al. 2020; Saavedra et al. 2022; Warkentin 1995). In this study, we examined the effects of predation risk on short-term as well as long-term traits such as fecundity and lifespan. In addition, we also compared the effects of exposure to predation risks for long versus short duration.

References

  1. Abrams, P.A. & Rowe, L. (1996) The effects of predation on the age and size of maturity of prey. Evolution, 50, 1052–1061.  https://doi.org/10.1111/j.1558-5646.1996.tb02346.x

  2. Choh, Y. & Takabayashi, J. (2010) Predator avoidance by phytophagous mites is affected by the presence of herbivores in a neighboring patch. Journal of Chemical Ecology, 36, 614–619.  https://doi.org/10.1007/s10886-010-9792-4

  3. Choh, Y., Uefune, M. & Takabayashi, J. (2010) Predation-related odours reduce oviposition in a herbivorous mite. Experimental and Applied Acarology, 50, 1–8.  https://doi.org/10.1007/s10493-009-9277-8

  4. Clinchy, M., Sheriff, M.J. & Zanette, L.Y. (2013) Predator-induced stress and the ecology of fear. Functional Ecology, 27, 56–65.  https://doi.org/10.1111/1365-2435.12007

  5. Freinschlag, J. & Schausberger, P. (2016) Predation risk-mediated maternal effects in the two-spotted spider mite, Tetranychus urticae. Experimental and Applied Acarology, 69, 35–47.  https://doi.org/10.1007/s10493-016-0014-9

  6. Grostal, P. & Dicke, M. (1999) Direct and indirect cues of predation risk influence behavior and reproduction of prey: a case for acarine interactions. Behavioral Ecology, 10, 422–427.  https://doi.org/10.1093/beheco/10.4.422

  7. Gurr, G.M., Wratten, S.D., Landis, D.A. & You, M. (2017) Habitat management to suppress pest populations: progress and prospects. Annual Review of Entomology, 62, 91–109.  https://doi.org/10.1146/annurev-ento-031616-035050

  8. Hawlena, D. & Schmitz, O.J. (2010) Herbivore physiological response to predation risk and implications for ecosystem nutrient dynamics. Proceedings of National Academy of Sciences of the United States of America, 107, 15503–15507.  https://doi.org/10.1073/pnas.1009300107

  9. Hercus, M.J., Loeschcke, V. & Rattan, S.I.S. (2003) Lifespan extension of Drosophila melanogaster through hormesis by repeated mild heat stress. Biogerontology, 4, 149–156.  https://doi.org/10.1023/A:1024197806855

  10. Hermann, S.L. & Thaler, J.S. (2014) Prey perception of predation risk : volatile chemical cues mediate non ‑ consumptive effects of a predator on a herbivorous insect. Oecologia, 176, 669–676.  https://doi.org/10.1007/s00442-014-3069-5

  11. Jiao, R., Xu, C., Yu, L., He, X.Z., Qiao, G., He, L. & Li, L. (2016) Prolonged coldness on eggs reduces immature survival and reproductive fitness in Tetranychus urticae (Acari: Tetranychidae). Systematic and Applied Acarology, 21, 1651–1661.  https://doi.org/10.11158/saa.21.12.6

  12. Li, G.-Y. & Zhang, Z.-Q. (2019) Development, lifespan and reproduction of spider mites exposed to predator-induced stress across generations. Biogerontology, 20, 871–882.  https://doi.org/10.1007/s10522-019-09835-0

  13. Majchrzak, Y.N., Peers, M.J.L., Studd, E.K., Menzies, A.K., Walker, P.D., Shiratsuru, S., McCaw, L.K., Boonstra, R., Humphries, M., Jung, T.S., Kenney, A.J., Krebs, C.J., Murray, D.L. & Boutin, S. (2022) Balancing food acquisition and predation risk drives demographic changes in snowshoe hare population cycles. Ecology Letters, 25, 981–991.  https://doi.org/10.1111/ele.13975

  14. McCauley, S.J., Rowe, L. & Fortin, M.-J. (2011) The deadly effects of “nonlethal” predators. Ecology, 92, 2043–2048.  https://doi.org/10.1890/11-0455.1

  15. Oku, K., Yano, S., Osakabe, M. & Takafuji, A. (2003) Spider mites assess predation risk by using the odor of injured conspecifics. Journal of Chemical Ecology, 29, 2609–2613.  https://doi.org/10.1023/A:1026395311664

  16. Oliveira, J.A. & Moraes, L.J.C.L. (2021) Mating behavior of Anolis punctatus ( Squamata : Dactyloidae ) in the Brazilian Amazonia. Phyllomedusa, 20, 185–190.  https://doi.org/10.11606/issn.2316-9079.v20i2p185-190

  17. Peckarsky, B.L., Mcintosh, A.R., Taylor, B.W. & Dahl, J. (2002) Predator chemicals induce changes in mayfliy life history traits: a whole-stream manipulation. Ecology, 83, 612–618.  https://doi.org/10.1890/0012-9658(2002)083[0612:PCICIM]2.0.CO;2

  18. Ristyadi, D., He, X.Z. & Wang, Q. (2022) Thermotolerance in a spider mite: implications in disinfestation treatment. Systematic and Applied Acarology, 27, 473–481.  https://doi.org/10.11158/saa.27.3.6

  19. Rocha, M.S., Celada, L.A., Rodrigues, E.N.L. & Costa-Schmidt, L.E. (2020) Under pressure: Predation risk defining mating investment in matured spider mite Tetranychus urticae. Systematic and Applied Acarology, 25, 1359–1372.  https://doi.org/10.11158/saa.25.8.1

  20. Saavedra, I., Tomás, G. & Amo, L. (2022) Assessing behavioral sex differences to chemical cues of predation risk while provisioning nestlings in a hole-nesting bird. bioRxiv, 482199.  https://doi.org/10.1101/2022.03.14.482199

  21. Škaloudová, B., Zemek, R. & Křivan, V. (2007) The effect of predation risk on an acarine system. Animal Behaviour, 74, 813–821.  https://doi.org/10.1016/j.anbehav.2007.02.005

  22. Skelhorn, J., Rowland, H.M., Delf, J., Speed, M.P. & Ruxton, G.D. (2011) Density-dependent predation in fl uences the evolution and behavior of masquerading prey. Proceedings of National Academy of Sciences of the United States of America, 108, 6532–6536.  https://doi.org/10.1073/pnas.1014629108

  23. Søvik, G. & Leinaas, H.P. (2003) Adult survival and reproduction in an arctic mite, Ameronothrus lineatus (Acari, Oribatida): Effects of temperature and winter cold. Canadian Journal of Zoology, 81, 1579–1588.  https://doi.org/10.1139/z03-113

  24. Stoks, R. (2001) Food stress and predator-induced stress shape developmental performance in a damselfly. Oecologia, 127, 222–229.  https://doi.org/10.1007/s004420000595

  25. Torson, A.S., Yocum, G.D., Rinehart, J.P., Kemp, W.P. & Bowsher, J.H. (2015) Transcriptional responses to fluctuating thermal regimes underpinning differences in survival in the solitary bee Megachile rotundata. The Journal of Experimental Biology, 218, 1060–1068.  https://doi.org/10.1242/jeb.113829

  26. Warkentin, K.M. (1995) in hatching age: A response. Proceedings of National Academy of Sciences of the United States of America, 92, 3507–3510.

  27. Wei, X. & Zhang, Z.-Q. (2022) Level-dependent effects of predation stress on prey development, lifespan and reproduction in mites. Biogerontology, 23, 515–527.  https://doi.org/10.1007/s10522-022-09980-z

  28. Wei, X. & Zhang, Z.Q. (2019) A modified Munger cell for testing long-Term effects of predator-induced stress on prey: An example using Tyrophagus putrescentiae (Acaridae) and its predator Neoseiulus cucumeris (Phytoseiidae). Systematic and Applied Acarology, 24, 2285–2289.  https://doi.org/10.11158/saa.24.12.1

  29. Wei, X.Y., Li, G.Y. & Zhang, Z.-Q. (2022a) Prey life stages modulate effects of predation stress on prey lifespan, development, and reproduction in mites. Insect Science. https://doi.org/10.1111/1744-7917.13124

  30. Wei, X.Y., Liu, J.F. & Zhang, Z.-Q. (2022b) Predation stress experienced as immature mites extends their lifespan. Biogerontology. https://doi.org/10.1007/s10522-022-09990-x

  31. Zanette, L.Y., White, A.F., Allen, M.C. & Clinchy, M. (2011) Perceived predation risk reduces the number of offspring songbirds produce per year. Science, 334, 1398–1401.  https://doi.org/10.1126/science.1210908

  32. Zhang, G.H., Li, Y.Y., Zhang, K.J., Wang, J.J., Liu, Y.Q. & Liu, H. (2016) Effects of heat stress on copulation, fecundity and longevity of newlyemerged adults of the predatory mite, Neoseiulus barkeri (Acari: Phytoseiidae). Systematic and Applied Acarology, 21, 295–306.  https://doi.org/10.11158/saa.21.3.5

  33. Zheng, J., Cheng, X., Ho, A.A., Zhang, B. & Ma, C. (2017) Are adult life history traits in oriental fruit moth a ff ected by a mild pupal heat stress ? Journal of Insect Physiology, 102, 36–41.  https://doi.org/10.1016/j.jinsphys.2017.09.004