Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Amplification of plant volatile defence against insect herbivory in a warming Arctic tundra

Abstract

Plant-emitted volatile organic compounds (VOCs) play fundamental roles in atmospheric chemistry and ecological processes by contributing to aerosol formation1 and mediating species interactions2. Rising temperatures and the associated shifts in vegetation composition have been shown to be the primary drivers of plant VOC emissions in Arctic ecosystems3. Although herbivorous insects also strongly alter plant VOC emissions2, no studies have addressed the impact of herbivory on plant VOC emissions in the Arctic. Here we show that warming dramatically increases the amount, and alters the blend, of VOCs released in response to herbivory. We observed that a tundra ecosystem subjected to warming, by open-top chambers, for 8 or 18 years showed a fourfold increase in leaf area eaten by insect herbivores. Herbivory by autumnal moth (Epirrita autumnata) larvae, and herbivory-mimicking methyl jasmonate application, on the widespread circumpolar dwarf birch (Betula nana) both substantially increased emissions of terpenoids. The long-term warming treatments and mimicked herbivory caused, on average, a two- and fourfold increase in monoterpene emissions, respectively. When combined, emissions increased 11-fold, revealing a strong synergy between warming and herbivory. The synergistic effect was even more pronounced for homoterpene emissions. These findings suggest that, in the rapidly warming Arctic, insect herbivory may be a primary determinant of VOC emissions during periods of active herbivore feeding.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Individual and joint impacts of in situ warming and mimicked herbivory on VOC emissions.
Fig. 2: Impacts of warming and mimicked herbivory on VOC blends.
Fig. 3: Time course of VOC induction.
Fig. 4: Impacts of in situ warming on background insect herbivory.

Similar content being viewed by others

Data availability

All VOC and background herbivory data that support the findings of this study are available in Figshare with the data DOI identifier https://doi.org/10.6084/m9.figshare.7879340.

References

  1. Jokinen, T. et al. Production of extremely low volatile organic compounds from biogenic emissions: measured yields and atmospheric implications. Proc. Natl Acad. Sci. USA 112, 7123–7128 (2015).

    Article  CAS  Google Scholar 

  2. Turlings, T. C. J. & Erb, M. Tritrophic interactions mediated by herbivore-induced plant volatiles: mechanisms, ecological relevance, and application potential. Annu. Rev. Entomol. 63, 433–452 (2018).

    Article  CAS  Google Scholar 

  3. Kramshoj, M. et al. Large increases in Arctic biogenic volatile emissions are a direct effect of warming. Nat. Geosci. 9, 349–352 (2016).

    Article  Google Scholar 

  4. Kesselmeier, J. et al. Volatile organic compound emissions in relation to plant carbon fixation and the terrestrial carbon budget. Glob. Biogeochem. Cycles 16, 73-1–73-9 (2002).

    Article  Google Scholar 

  5. Dicke, M., van Loon, J. J. A. & Soler, R. Chemical complexity of volatiles from plants induced by multiple attack. Nat. Chem. Biol. 5, 317–324 (2009).

    Article  CAS  Google Scholar 

  6. Vickers, C. E., Gershenzon, J., Lerdau, M. T . & Loreto, F.A. A unified mechanism of action for volatile isoprenoids in plant abiotic stress. Nat. Chem. Biol. 5, 283–291 (2009).

    Article  CAS  Google Scholar 

  7. Peñuelas, J. & Staudt, M. BVOCs and global change. Trends Plant Sci. 15, 133–144 (2010).

    Article  Google Scholar 

  8. Kessler, A. & Baldwin, I. T. Defensive function of herbivore-induced plant volatile emissions in nature. Science 291, 2141–2144 (2001).

    Article  CAS  Google Scholar 

  9. Holopainen, J. K., Kivimäenpää, M. & Nizkorodov, S. A. Plant-derived secondary organic material in the air and ecosystems. Trends Plant Sci. 22, 744–753 (2017).

    Article  CAS  Google Scholar 

  10. Ehn, M. et al. A large source of low-volatility secondary organic aerosol. Nature 506, 476–479 (2014).

    Article  CAS  Google Scholar 

  11. IPCC Climate Change 2014: Synthesis Report (eds Pachauri, R. K. et al.) (Cambridge Univ. Press, 2014).

  12. Potosnak, M. J. et al. Isoprene emissions from a tundra ecosystem. Biogeosciences 10, 871–889 (2013).

    Article  Google Scholar 

  13. Valolahti, H., Kivimäenpää, M., Faubert, P., Michelsen, A. & Rinnan, R. Climate change-induced vegetation change as a driver of increased subarctic biogenic volatile organic compound emissions. Glob. Change Biol. 21, 3478–3488 (2015).

    Article  Google Scholar 

  14. Tang, J., Valolahti, H., Kivimäenpää, M., Michelsen, A. & Rinnan, R. Acclimation of biogenic volatile organic compound emission from subarctic heath under long-term moderate warming. J. Geophys. Res. Biogeosci. 123, 95–105 (2018).

    Article  CAS  Google Scholar 

  15. Ameye, M. et al. Green leaf volatile production by plants: a meta-analysis. New Phytol. 220, 666–683 (2018).

    Article  CAS  Google Scholar 

  16. Rowen, E. & Kaplan, I. Eco-evolutionary factors drive induced plant volatiles: a meta-analysis. New Phytol. 210, 284–294 (2016).

    Article  CAS  Google Scholar 

  17. Bergström, R., Hallquist, M., Simpson, D., Wildt, J. & Mentel, T. F. Biotic stress: a significant contributor to organic aerosol in Europe? Atmos. Chem. Phys. 14, 13643–13660 (2014).

    Article  Google Scholar 

  18. Deutsch, C. A. et al. Increase in crop losses to insect pests in a warming climate. Science 361, 916–919 (2018).

    Article  CAS  Google Scholar 

  19. Post, E. et al. Ecological dynamics across the Arctic associated with recent climate change. Science 325, 1355–1358 (2009).

    Article  CAS  Google Scholar 

  20. Lesk, C., Coffel, E., D’Amato, A. W., Dodds, K. & Horton, R. Threats to North American forests from southern pine beetle with warming winters. Nat. Clim. Change 7, 713–717 (2017).

    Article  Google Scholar 

  21. Barrio, I. C., Bueno, C. G. & Hik, D. S. Warming th e tundra: reciprocal responses of invertebrate herbivores and plants. Oikos 125, 20–28 (2016).

    Article  Google Scholar 

  22. Jepsen, J. U. et al. Rapid northwards expansion of a forest insect pest attributed to spring phenology matching with sub-Arctic birch. Glob. Change Biol. 17, 2071–2083 (2011).

    Article  Google Scholar 

  23. Sistla, S. A. et al. Long-term warming restructures Arctic tundra without changing net soil carbon storage. Nature 497, 615–618 (2013).

    Article  CAS  Google Scholar 

  24. Hollesen, J. et al. Winter warming as an important co-driver for Betula nana growth in western Greenland during the past century. Glob. Change Biol. 21, 2410–2423 (2015).

    Article  Google Scholar 

  25. Schuman, M. C., Heinzel, N., Gaquerel, E., Svatos, A. & Baldwin, I. T. Polymorphism in jasmonate signaling partially accounts for the variety of volatiles produced by Nicotiana attenuata plants in a native population. New Phytol. 183, 1134–1148 (2009).

    Article  CAS  Google Scholar 

  26. Barrio, I. C. et al. Background invertebrate herbivory on dwarf birch (Betula glandulosa– nana complex) increases with temperature and precipitation across the tundra biome. Polar Biol. 40, 2265–2278 (2017).

    Article  Google Scholar 

  27. Kozlov, M. V., Lanta, V., Zverev, V. & Zvereva, E. L. Global patterns in background losses of woody plant foliage to insects. Glob. Ecol. Biogeogr. 24, 1126–1135 (2015).

    Article  Google Scholar 

  28. Halitschke, R., Stenberg, J. A., Kessler, D., Kessler, A. & Baldwin, I. T. Shared signals—‘alarm calls’ from plants increase apparency to herbivores and their enemies in nature. Ecol. Lett. 11, 24–34 (2008).

    PubMed  Google Scholar 

  29. Mentel, T. F. et al. Secondary aerosol formation from stress-induced biogenic emissions and possible climate feedbacks. Atmos. Chem. Phys. 13, 8755–8770 (2013).

    Article  Google Scholar 

  30. Paasonen, P. et al. Warming-induced increase in aerosol number concentration likely to moderate climate change. Nat. Geosci. 6, 438–442 (2013).

    Article  CAS  Google Scholar 

  31. Abisko Scientific Research Station. Temperature and precipitation data 1913–2015 (Polarforskningssekretariatet Press, 2016).

  32. Tholl, D. et al. Practical approaches to plant volatile analysis. Plant J. 45, 540–560 (2006).

    Article  CAS  Google Scholar 

  33. Johnsen, L. G., Skou, P. B., Khakimov, B. & Bro, R. Gas chromatography–mass spectrometry data processing made easy. J. Chromatogr. A 1503, 57–64 (2017).

    Article  CAS  Google Scholar 

  34. Guenther, A. B., Zimmerman, P. R., Harley, P. C., Monson, R. K. & Fall, R. Isoprene and monoterpene emission rate variability: model evaluations and sensitivity analyses. J. Geophys. Res. Atmos. 98, 12609–12617 (1993).

    Article  Google Scholar 

  35. Schuman, M. C., Allmann, S. & Baldwin, I. T. Plant defense phenotypes determine the consequences of volatile emission for individuals and neighbors. eLife 4, e04490 (2015).

    Article  Google Scholar 

  36. Graus, M., Müller, M. & Hansel, A. High resolution PTR–TOF: quantification and formula confirmation of VOC in real time. J. Am. Soc. Mass Spectrom. 21, 1037–1044 (2010).

    Article  CAS  Google Scholar 

  37. Holzinger, R. PTRwid: a new widget tool for processing PTR–TOF–MS data. Atmos. Meas. Tech. 8, 3903–3922 (2015).

    Article  Google Scholar 

  38. Kozlov, M. V., Filippov, B. Y., Zubrij, N. A. & Zverev, V. Abrupt changes in invertebrate herbivory on woody plants at the forest–tundra ecotone. Polar Biol. 38, 967–974 (2015).

    Article  Google Scholar 

  39. R Core Team. R: A Language and Environment for Statistical Computing (R Foundation for Statistical Computing, 2009).

  40. Oksanen, J. F. et al. Vegan: Community ecology package v.2.0-5 (CRAN, 2012); http://CRAN.R-project.org/package=vegan

  41. Brückner, A. & Heethoff, M. A chemo-ecologists’ practical guide to compositional data analysis. Chemoecology 27, 33–46 (2017).

    Article  Google Scholar 

Download references

Acknowledgements

We thank M. Jylkkä for providing the image of E. autumnata and C.L. Davie-Martin for language editing. We gratefully acknowledge financial support from the Danish Council for Independent Research/Natural Sciences, the Danish National Research Foundation (grant No. CENPERM DNRF100), the Marie Sklodowska-Curie grant (No. 751684) and the European Research Council (grant No. 771012) under the European Union’s Horizon 2020 research and innovation programme. The Abisko Scientific Research Station (Sweden) is thanked for housing and logistics support.

Author information

Authors and Affiliations

Authors

Contributions

T.L. and R.R. designed the experiment. A.M. established the experimental site. T.L. and T.H. developed the methodology for the volatile emission time course experiments. T.L. collected, analysed and interpreted the data and wrote the manuscript. All authors commented on the manuscript and approved the final version.

Corresponding author

Correspondence to Tao Li.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Journal Peer Review Information: Nature Plants thanks Robert Hollister and the other anonymous reviewers for their contribution to the peer review of this work.

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary information

Supplementary Figs. 1–10.

Reporting Summary.

Supplementary Tables 1–6

Supplementary Table 1: VOC emissions of Betula nana under different treatments. Supplementary Table 2: Summary of mixed-effects models testing for main warming and mimicked herbivory effects and their interactions. Supplementary Table 3: Summary of Kruskal–Wallis tests for warming and herbivory effects. Supplementary Table 4: Timelines of real time measurements of VOC emissions. Supplementary Table 5: List of ion masses and molecular formulae measured with the PTR–ToF–MS. Supplementary Table 6: Summary of mixed-effects models testing for warming, litter addition, herbivory effects and their interactions.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Li, T., Holst, T., Michelsen, A. et al. Amplification of plant volatile defence against insect herbivory in a warming Arctic tundra. Nat. Plants 5, 568–574 (2019). https://doi.org/10.1038/s41477-019-0439-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41477-019-0439-3

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing