Hostname: page-component-8448b6f56d-c4f8m Total loading time: 0 Render date: 2024-04-20T04:31:02.584Z Has data issue: false hasContentIssue false

Mechanical stimulation from plant contact and wind negatively impact pea aphids (Hemiptera: Aphididae) indirectly through host plants

Published online by Cambridge University Press:  27 August 2019

Tyler J. Follman
Affiliation:
Department of Entomology, North Dakota State University, Fargo, North Dakota, 58103, United States of America
Aleix Valls
Affiliation:
Department of Entomology, North Dakota State University, Fargo, North Dakota, 58103, United States of America
Katherine C. Kral-O’Brien*
Affiliation:
Department of Entomology, North Dakota State University, Fargo, North Dakota, 58103, United States of America
Jason P. Harmon
Affiliation:
Department of Entomology, North Dakota State University, Fargo, North Dakota, 58103, United States of America
*
1Corresponding author (e-mail: kralx009@gmail.com)

Abstract

Global change research has shown how altering factors like temperature and precipitation can impact insect ecology. However, despite global changes in wind patterns, the effects of altering wind have been relatively unexplored, and even less is understood about indirect effects on insects. To better understand indirect effects of wind on pea aphids (Acyrthosiphon pisum (Harris); Hemiptera: Aphididae), we performed two experiments using different techniques for simulating mechanical stimulation effects from wind. First, we used either a brush or leaf to simulate plant-to-plant contact caused by wind. Then we tested the indirect effects of wind by distinguishing between wind and wind plus plant contact produced by adjacent plants. In the first experiment, aphid fecundity was reduced on plants with the leaf-to-plant treatment compared to the control. In the second experiment, wind treatments reduced pea aphid fecundity, but wind did not interact with plant density. Our results further the idea that altering wind patterns can influence plant–insect interactions. We also show that more research is necessary to disentangle how and why wind indirectly influences herbivores. Future research should focus on how pea aphid responses to wind change due to the methodology of wind exposure and interactions with additional biotic and abiotic factors.

Type
Behaviour and Ecology
Copyright
© Entomological Society of Canada 2019 

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.)

Footnotes

Subject editor: Chandra Moffat

References

Anten, N.P., Alcalá-Herrera, R., Schieving, F., and Onoda, Y. 2010. Wind and mechanical stimuli differentially affect leaf traits in Plantago major . New Phytologist, 188: 554564. https://doi.org/10.1111/j.1469-8137.2010.03379.x.CrossRefGoogle ScholarPubMed
Atkinson, N.J. and Urwin, P.E. 2012. The interaction of plant biotic and abiotic stresses: from genes to the field. Journal of Experimental Botany, 63: 35233543. https://doi.org/10.1093/jxb/ers100.CrossRefGoogle ScholarPubMed
Barton, B.T. 2014. Reduced wind strengthens topdown control of an insect herbivore. Ecology, 95: 23752381. https://doi.org/10.1890/13-2171.1.CrossRefGoogle Scholar
Barton, B.T. 2017. Beyond global warming: putting the “climate” back into “climate change ecology”. Food Webs, 13: 5152. https://doi.org/10.1016/j.fooweb.2017.03.002.CrossRefGoogle Scholar
Bornette, G. and Puijalon, S. 2011. Response of aquatic plants to abiotic factors: a review. Aquatic Sciences, 73: 114. https://doi.org/10.1007/s00027-010-0162-7.CrossRefGoogle Scholar
Chen, C., Biere, A., Gols, R., Halfwerk, W., van Oers, K., and Harvey, J.A. 2018. Responses of insect herbivores and their food plants to wind exposure and the importance of predation risk. Journal of Animal Ecology, 87: 10461057. https://doi.org/10.1111/1365-2656.12835.CrossRefGoogle ScholarPubMed
Cherry, M.J. and Barton, B.T. 2017. Effects of wind on predator-prey interactions. Food Webs, 13: 9297. https://doi.org/10.1016/j.fooweb.2017.02.005.CrossRefGoogle Scholar
Cipollini, D.F. 1997. Wind-induced mechanical stimulation increases pest resistance in common bean. Oecologia, 111: 8490. https://doi.org/10.1007/s004420050211.CrossRefGoogle ScholarPubMed
de Langre, E. 2008. Effects of wind on plants. Annual Review of Fluid Mechanics, 40: 141168. https://doi.org/10.1146/annurev.fluid.40.111406.102135.CrossRefGoogle Scholar
Dixon, A.F.G. 2005. Insect herbivore-host dynamics: tree-dwelling aphids. Cambridge University Press, Cambridge, United Kingdom.CrossRefGoogle Scholar
Gardiner, B., Berry, P., and Moulia, B. 2016. Wind impacts on plant growth, mechanics and damage. Plant Science, 245: 94118. https://doi.org/10.1016/j.plantsci.2016.01.006.CrossRefGoogle ScholarPubMed
Gwynn, D.M., Callaghan, A., Gorham, J., Walters, K.F.A., and Fellowes, M.D.E. 2005. Resistance is costly: trade-offs between immunity, fecundity and survival in the pea aphid. Proceedings of the Royal Society of London B: Biological Sciences, 272: 18031808. https://doi.org/10.1098/rspb.2005.3089.CrossRefGoogle ScholarPubMed
Hirabayashi, Y., Mahendran, R., Koirala, S., Konoshima, L., Yamazaki, D., Watanabe, S., et al. 2013. Global flood risk under climate change. Nature Climate Change, 3: 816821. https://doi.org/10.1038/nclimate1911.CrossRefGoogle Scholar
Markovic, D., Glinwood, R., Olsson, U., and Ninkovic, V. 2014. Plant response to touch affects the behaviour of aphids and ladybirds. Arthropod-Plant Interactions, 8: 171181. https://doi.org/10.1007/s11829-014-9303-6.CrossRefGoogle Scholar
Markovic, D., Nikolic, N., Glinwood, R., Seisenbaeva, G., and Ninkovic, V. 2016. Plant responses to brief touching: a mechanism for early neighbour detection? Public Library of Science One, 11: e0165742. https://doi.org/10.1371/journal.pone.0165742.Google ScholarPubMed
McVicar, T.R., Roderick, M.L., Donohue, R.J., Li, L.T., Van Niel, T.G., Thomas, A., et al. 2012. Global review and synthesis of trends in observed terrestrial near-surface wind speeds: implications for evaporation. Journal of Hydrology, 416–417: 182205. https://doi.org/10.1016/j.jhydrol.2011.10.024.CrossRefGoogle Scholar
Miura, T., Braendle, C., Shingleton, A., Sisk, G., Kambhampati, S., and Stern, D.L. 2003. A comparison of parthenogenetic and sexual embryogenesis of the pea aphid Acyrthosiphon pisum (Hemiptera: Aphidoidea). Journal of Experimental Zoology Part B: Molecular and Developmental Evolution, 295: 5981. https://doi.org/10.1002/jez.b.3.CrossRefGoogle Scholar
Moran, P.J. and Cipollini, D.F. 1999. Effect of wind-induced mechanical stress on soluble peroxidase activity and resistance to pests in cucumber. Journal of Phytopathology, 147: 313316.CrossRefGoogle Scholar
Parmesan, C. 2006. Ecological and evolutionary responses to recent climate change. Annual Review of Ecology, Evolution, and Systematics, 37: 637669. https://doi.org/10.1146/annurev.ecolsys.37.091305.110100.CrossRefGoogle Scholar
SAS Institute. 2017. JMP, version 13.2.1. SAS Institute, Cary, North Carolina, United States of America.Google Scholar
Simon, J.C., Boutin, S., Tsuchida, T., Koga, R., Le Gallic, J.F., Frantz, A., et al. 2011. Facultative symbiont infections affect aphid reproduction. Public Library of Science One, 6: p.e21831. https://doi.org/10.1371/journal.pone.0021831.Google ScholarPubMed
Speights, C.J., Harmon, J.P., and Barton, B.T. 2017. Contrasting the potential effects of daytime versus nighttime warming on insects. Current Opinion in Insect Science, 23: 16. https://doi.org/10.1016/j.cois.2017.06.005.CrossRefGoogle ScholarPubMed
Stoddard, F.L., Nicholas, A.H., Rubiales, D., Thomas, J., and Villegas-Fernández, A.M. 2010. Integrated pest management in faba bean. Field Crops Research, 115: 308318. https://doi.org/10.1016/j.fcr.2009.07.002.CrossRefGoogle Scholar
van Emden, H.F., Macklin, R.J., and Staunton-Lambert, S. 1990. Stroking plants to reduce aphid populations. Entomologist, 109: 184188.Google Scholar
Vasseur, D.A., DeLong, J.P., Gilbert, B., Greig, H.S., Harley, C.D., McCann, K.S., et al. 2014. Increased temperature variation poses a greater risk to species than climate warming. Proceedings of the Royal Society of London B: Biological Sciences, 281: 20132612. https://doi.org/10.1098/rspb.2013.2612.CrossRefGoogle ScholarPubMed
Vautard, R., Cattiaux, J., Yiou, P., Thépaut, J.N., and Ciais, P. 2010. Northern Hemisphere atmospheric stilling partly attributed to an increase in surface roughness. Nature Geoscience, 3: 756761. https://doi.org/10.1038/NGEO979.CrossRefGoogle Scholar
Wu, Z., Dijkstra, P., Koch, G.W., Peñuelas, J., and Hungate, B.A. 2011. Responses of terrestrial ecosystems to temperature and precipitation change: a meta-analysis of experimental manipulation. Global Change Biology, 17: 927942.CrossRefGoogle Scholar
Zhao, Z., Luo, Y., and Jiang, Y. 2017. Is global strong wind declining? Collection of Advances in Climate Change Research, 2: 225228. https://doi.org/10.3724/SP.J.1248.2011.00225.CrossRefGoogle Scholar