Article

A statistical estimator for determining the limits of contemporary and historic phenology

  • Nature Ecology & Evolution 118761882 (2017)
  • doi:10.1038/s41559-017-0350-0
  • Download Citation
Received:
Accepted:
Published online:

Abstract

Climate change affects not just where species are found, but also when species’ key life-history events occur—their phenology. Measuring such changes in timing is often hampered by a reliance on biased survey data: surveys identify that an event has taken place (for example, the flower is in bloom), but not when that event happened (for example, the flower bloomed yesterday). Here, we show that this problem can be circumvented using statistical estimators, which can provide accurate and unbiased estimates from sparsely sampled observations. We demonstrate that such methods can resolve an ongoing debate about the relative timings of the onset and cessation of flowering, and allow us to place modern observations reliably within the context of the vast wealth of historical data that reside in herbaria, museum collections, and written records. We also analyse large-scale citizen science data from the United States National Phenology Network and reveal not just earlier but also potentially more variable flowering in recent years. Evidence for greater variability through time is important because increases in variation are characteristic of systems approaching a state change.

  • Subscribe to Nature Ecology & Evolution for full access:

    $99

    Subscribe

Additional access options:

Already a subscriber?  Log in  now or  Register  for online access.

References

  1. 1.

    IPCC Climate Change 2014: Synthesis Report (eds Core Writing Team, Pachauri, R. K. & Meyer L. A.) (Cambridge Univ. Press, Cambridge, 2015).

  2. 2.

    Menzel, A. et al. European phenological response to climate change matches the warming pattern. Glob. Change Biol. 12, 1969–1976 (2006).

  3. 3.

    Parmesan, C. et al. Ecological and evolutionary responses to recent climate change. Annu. Rev. Ecol. Evol. Syst. 37, 637–669 (2006).

  4. 4.

    Wolkovich, E. M. et al. Warming experiments underpredict plant phenological responses to climate change. Nature 485, 494–497 (2012).

  5. 5.

    Silvertown, J. A new dawn for citizen science. Trends Ecol. Evol. 24, 467–471 (2009).

  6. 6.

    Pyke, G. H. & Ehrlich, P. R. Biological collections and ecological/environmental research: a review, some observations and a look to the future. Biol. Rev. 85, 247–266 (2010).

  7. 7.

    Robbirt, K. M., Davy, A. J., Hutchings, M. J. & Roberts, D. L. Validation of biological collections as a source of phenological data for use in climate change studies: a case study with the orchid ophrys sphegodes. J. Ecol. 99, 235–241 (2011).

  8. 8.

    Baird, R. C. Leveraging the fullest potential of scientific collections through digitisation. Biodivers. Informatics 7, 130–136 (2010).

  9. 9.

    Beaman, R. S. & Cellinese, N. Mass digitization of scientific collections: new opportunities to transform the use of biological specimens and underwrite biodiversity science. ZooKeys 209, 7–17 (2012).

  10. 10.

    Balke, M. et al. Biodiversity into your hands: a call for a virtual global natural history ‘metacollection’. Front. Zool. 10, 55 (2013).

  11. 11.

    Willis, C. G. et al. Crowdcurio: an online crowdsourcing platform to facilitate climate change studies using herbarium specimens. New Phytol. 215, 479–488 (2017).

  12. 12.

    Meyer, C., Weigelt, P. & Kreft, H. Multidimensional biases, gaps and uncertainties in global plant occurrence information. Ecol. Lett. 19, 992–1006 (2016).

  13. 13.

    Roberts, D. L. & Solow, A. R. Flightless birds: when did the dodo become extinct? Nature 426, 245–245 (2003).

  14. 14.

    Ruggles, R. & Brodie, H. An empirical approach to economic intelligence in World War II. J. Am. Stat. Assoc. 42, 72–91 (1947).

  15. 15.

    Cooke, P. Optimal linear estimation of bounds of random variables. Biometrika 67, 257–258 (1980).

  16. 16.

    Weissman, I. Confidence intervals for the threshold parameter. Commun. Stat. Theory Methods 10, 549–557 (1981).

  17. 17.

    Inouye, D. W. Effects of climate change on phenology, frost damage, and floral abundance of montane wildflowers. Ecology 89, 353–362 (2008).

  18. 18.

    Aldridge, G., Inouye, D. W., Forrest, J. R., Barr, W. A. & Miller-Rushing, A. J. Emergence of a mid-season period of low floral resources in a montane meadow ecosystem associated with climate change. J. Ecol. 99, 905–913 (2011).

  19. 19.

    CaraDonna, P. J., Iler, A. M. & Inouye, D. W. Shifts in flowering phenology reshape a subalpine plant community. Proc. Natl Acad. Sci. USA 111, 4916–4921 (2014).

  20. 20.

    Visser, M. E. & Both, C. Shifts in phenology due to global climate change: the need for a yardstick. Proc. R. Soc. B 272, 2561–2569 (2005).

  21. 21.

    Miller-Rushing, A. J., Inouye, D. W. & Primack, R. B. How well do first flowering dates measure plant responses to climate change? The effects of population size and sampling frequency. J. Ecol. 96, 1289–1296 (2008).

  22. 22.

    Davis, C. C., Willis, C. G., Connolly, B., Kelly, C. & Ellison, A. M. Herbarium records are reliable sources of phenological change driven by climate and provide novel insights into species phenological cueing mechanisms. Am. J. Bot. 102, 1599–1609 (2015).

  23. 23.

    Papworth, S., Rist, J., Coad, L. & Milner-Gulland, E. Evidence for shifting baseline syndrome in conservation. Conserv. Lett. 2, 93–100 (2009).

  24. 24.

    Cook, B. I. et al. Sensitivity of spring phenology to warming across temporal and spatial climate gradients in two independent databases. Ecosystems 15, 1283–1294 (2012).

  25. 25.

    Gelman, A., Carlin, J. B., Stern, H. S. & Rubin, D. B. Bayesian Data Analysis 3rd edn (CRC Press, Boca Raton, 2014).

  26. 26.

    Scheffer, M., Carpenter, S., Foley, J. A., Folke, C. & Walker, B. Catastrophic shifts in ecosystems. Nature 413, 591–596 (2001).

  27. 27.

    Scheffer, M. et al. Early-warning signals for critical transitions. Nature 461, 53–59 (2009).

  28. 28.

    Körner, C. & Basler, D. Phenology under global warming. Science 327, 1461–1462 (2010).

  29. 29.

    Cook, B. I., Wolkovich, E. M. & Parmesan, C. Divergent responses to spring and winter warming drive community level flowering trends. Proc. Natl Acad. Sci. USA 109, 9000–9005 (2012).

  30. 30.

    Brooks, S. J., Self, A., Toloni, F. & Sparks, T. Natural history museum collections provide information on phenological change in british butterflies since the late-nineteenth century. Int. J. Biometeorol. 58, 1749–1758 (2014).

  31. 31.

    R Core Team R: A Language and Environment for Statistical Computing (R Foundation for Statistical Computing, Vienna, 2016); https://www.R-project.org/

  32. 32.

    Clements, C. F. et al. Experimentally testing the accuracy of an extinction estimator: Solow’s optimal linear estimation model. J. Anim. Ecol. 82, 345–354 (2013).

  33. 33.

    Therneau, T. deming: Deming, Thiel-Sen and Passing-Bablock Regression. R package version 1.0-1 (R Foundation for Statistical Computing, Vienna, 2014); https://CRAN.R-project.org/package=deming.

  34. 34.

    Miller-Rushing, A. J. & Primack, R. B. Global warming and flowering times in Thoreau’s Concord: a community perspective. Ecology 89, 332–341 (2008).

  35. 35.

    Willis, C. G., Ruhfel, B., Primack, R. B., Miller-Rushing, A. J. & Davis, C. C. Phylogenetic patterns of species loss in Thoreau’s woods are driven by climate change. Proc. Natl Acad. Sci. USA 105, 17029–17033 (2008).

  36. 36.

    Harris, I., Jones, P., Osborn, T. & Lister, D. Updated high-resolution grids of monthly climatic observations–the CRU TS3. 10 dataset. Int. J. Climatol. 34, 623–642 (2014).

  37. 37.

    Carpenter, B. et al. Stan: a probabilistic programming language. J. Stat. Softw. 76, 1–32 (2017).

  38. 38.

    Ellwood, E. R., Temple, S. A., Primack, R. B., Bradley, N. L. & Davis, C. C. Record-breaking early flowering in the eastern United States. PLoS ONE 8, e53788 (2013).

  39. 39.

    Gelman, A. & Pardoe, I. Bayesian measures of explained variance and pooling in multilevel (hierarchical) models. Technometrics 48, 241–251 (2006).

Download references

Acknowledgements

We thank the volunteers of the NPN for data collection. W.D.P. and T.J.D. were funded by Fonds de Recherche Nature et Technologies grant number 168004. The Colorado data collection was supported by National Science Foundation grants DEB 75-15422, DEB 78-07784, BSR 81-08387, DEB 94-08382, IBN 98-14509, DEB 02-38331 and DEB 09-22080 to D.W.I. We are grateful to D. Roberts and A. Solow for helping to calculate the s.e. of estimates of timing, and E. L. Wolkovich and B. G. Waring for comments on the paper. We also thank the photographers whose images we used in Fig. 3.

Author information

Affiliations

  1. Department of Biology, McGill University, Montréal, Québec, H3A 1B1, Canada

    • William D. Pearse
    •  & T. Jonathan Davies
  2. Department of Biological Sciences, Université du Québec à Montréal, Montréal, Québec, H2X 1Y4, Canada

    • William D. Pearse
  3. Department of Biology and Ecology Center, Utah State University, 5305 Old Main Hill, Logan, UT, 84322, USA

    • William D. Pearse
  4. Department of Organismic and Evolutionary Biology and Harvard University Herbaria, Harvard University, 22 Divinity Avenue, Cambridge, MA, 02138, USA

    • Charles C. Davis
  5. Department of Biology, University of Maryland, College Park, MD, 20742, USA

    • David W. Inouye
  6. Rocky Mountain Biological Laboratory, PO Box 519, Crested Butte, CO, 81224, USA

    • David W. Inouye
  7. Biology Department, Boston University, 5 Cummington Street, Boston, MA, 02215, USA

    • Richard B. Primack

Authors

  1. Search for William D. Pearse in:

  2. Search for Charles C. Davis in:

  3. Search for David W. Inouye in:

  4. Search for Richard B. Primack in:

  5. Search for T. Jonathan Davies in:

Contributions

W.D.P., T.J.D. and C.C.D. conceived of the study. W.D.P. analysed the data. All authors wrote the manuscript and interpreted the results.

Competing interests

The authors declare no competing financial interests.

Corresponding authors

Correspondence to William D. Pearse or T. Jonathan Davies.

Electronic supplementary material

  1. Supplementary Information

    Supplementary Figures 1–4, Supplementary Tables 1–8, Supplementary Reference

  2. Life Sciences Reporting Summary