Polar Biology

, Volume 40, Issue 3, pp 553–561 | Cite as

A race against time: habitat alteration by snow geese prunes the seasonal sequence of mosquito emergence in a subarctic brackish landscape

  • John S. Park
Original Paper


Species compositions in highly seasonal habitats often exhibit predictable patterns through time. However, the roles that ecological interactions play in shaping the sequence of species phenologies through a season are largely unexplored. Across the tundra on the Hudson Bay Lowlands, extensive foraging by lesser snow goose populations has been driving alterations to the landscape. Here, I show that this widespread and dramatic disturbance increases evaporation rates of ephemeral ponds and consequently constricts the temporal availability of seasonal aquatic habitats for larval mosquitoes. I also show that this constriction decreases the temporal diversity of closely related univoltine mosquito species that have varying emergence schedules. Three species of mosquitoes emerged through the season from four sampled ephemeral ponds associated with no goose grubbing; only one species emerged, early in the season, from the four ponds that experienced heavy grubbing. This study demonstrates a mechanism for temporal composition change in a ubiquitous and abundant group of arthropods on the tundra. It does not show life history evolution of emergence time of mosquitoes; however, it highlights the rather unexplored role of ecological interactions in altering the diversity of phenologies across seasonal time.


Seasonal ecology Life history strategies Temporal diversity Tundra 



I thank Stephen C. Stearns for his guidance and Marta M. Wells for her support. I thank R. J. Pupedis and Yale Peabody Museum of Natural History’s Division of Entomology for their generous support with equipment. L. E. Munstermann at Yale School of Public Health and S. K. Burian provided important suggestions for study design. L. E. Munstermann also aided in mosquito species identification. This project is indebted to the support and good company of D. T. Iles, D. N. Koons, R. F. Rockwell, L. M. Aubry, C. P. Mulder, and J. F. House in the field at LPB. Financial support for this project was provided by the Sherwood E. Silliman Fellowship from Yale University.

Supplementary material

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Supplementary material 1 (XLSX 11 kb)
300_2016_1978_MOESM2_ESM.pdf (187 kb)
Supplementary material 2 (PDF 187 kb)
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Supplementary material 3 (XLSX 11 kb)


  1. Adler PB, Lauenroth WK (2003) The power of time: spatiotemporal scaling of species diversity. Ecol Lett 6:749–756CrossRefGoogle Scholar
  2. Adler PB, White EP, Lauenroth WK, Kaufman DM, Rassweiler A, Rusak JA (2005) Evidence for a general species-time-area relationship. Ecology 86:2032–2039CrossRefGoogle Scholar
  3. Alisauskas RT, Rockwell RF, Dufour KW, Cooch EG, Zimmerman G, Drake KL, Leafloor JO, Moser TJ, Reed ET (2011) Harvest, survival, and abundance of midcontinent lesser snow geese relative to population reduction efforts. Wildl Monogr 179:1–42CrossRefGoogle Scholar
  4. Baker MC (1977) Shorebird food habits in the eastern Canadian Arctic. Condor 79:56–62CrossRefGoogle Scholar
  5. Bazzanti M, Seminara M, Baldoni S (1997) Chironomids (Diptera: Chironomidae) from three temporary ponds of different wet phase duration in central Italy. J Fresh Ecol 12:89–99CrossRefGoogle Scholar
  6. Bentley MD, Day JF (1989) Chemical ecology and behavioral aspects of mosquito oviposition. Annu Rev Entomol 34:401–421CrossRefPubMedGoogle Scholar
  7. Chesson P (2000) Mechanisms of maintenance of species diversity. Annu Rev Ecol Syst 31:343–366CrossRefGoogle Scholar
  8. Clark TM, Flis BJ, Remold SK (2004) Differences in the effects of salinity on larval growth and developmental programs of a freshwater and a euryhaline mosquito species (Insecta: Diptera, Culicidae). J Exp Biol 207:2289–2295CrossRefPubMedGoogle Scholar
  9. Coulson SJ, Hodkinson ID, Webb NR (2003) Aerial dispersal of invertebrates over a high-Arctic glacier foreland: Midtre Lovénbreen, Svalbard. Polar Biol 26:530–537CrossRefGoogle Scholar
  10. Danks HV (1981) Arctic arthropods: a review of systematics and ecology with particular reference to the North American fauna. Entomol Society of Canada, OttawaGoogle Scholar
  11. Danks HV (2002) Modification of adverse conditions by insects. Oikos 99:10–24CrossRefGoogle Scholar
  12. Darsie RF, Ward RA (2004) Identification and geographical distribution of the mosquitoes of North America, North of Mexico. University Press of Florida, GainesvilleGoogle Scholar
  13. Drake M (2001) The importance of temporary waters for Diptera (true-flies). Freshw Forum 17:26–39Google Scholar
  14. Gaston AJ, Elliott KH (2013) Effects of climate-induced changes in parasitism, predation and predator–predator interactions on reproduction and survival of an Arctic marine bird. Arctic 66:43–51CrossRefGoogle Scholar
  15. Gaston AJ, Hipfner JM, Campbell D (2002) Heat and mosquitoes cause breeding failures and adult mortality in an Arctic-nesting seabird. Ibis 144:185–191CrossRefGoogle Scholar
  16. Giannini TC, Chapman DS, Saraiva AM, Alves-dos-Santos I, Biesmeijer JC (2013) Improving species distribution models using biotic interactions: a case study of parasites, pollinators and plants. Ecography 36:649–656CrossRefGoogle Scholar
  17. Gjullin CM, Sailer RI, Stone A, Travis BV (1961) The Mosquitoes of Alaska. Agricultural Research Service, U.S Dept. of Agriculture, WashingtonGoogle Scholar
  18. Godsoe W, Harmon LJ (2012) How do species interactions affect species distribution models? Ecography 35:811–820CrossRefGoogle Scholar
  19. Handa IT, Harmsen R, Jefferies RL (2002) Patterns of vegetation change and the recovery potential of degraded areas in a coastal marsh system of the Hudson Bay lowlands. J Ecol 90:86–99CrossRefGoogle Scholar
  20. Haufe W, Burgess L (1956) Development of Aedes (Diptera: Culicidae) at Fort Churchill, Manitoba, and prediction of dates of emergence. Ecology 37:500–519CrossRefGoogle Scholar
  21. Hodkinson ID, Coulson SJ, Webb NR, Block W, Strathdee AT, Bale JS, Worland MR (1996) Temperature and the biomass of flying midges (Diptera: Chironomidae) in the high Arctic. Oikos 75:241–248CrossRefGoogle Scholar
  22. Jefferies RL, Rockwell RF (2002) Foraging geese, vegetation loss and soil degradation in an Arctic salt marsh. Appl Veg Sci 5:7–16CrossRefGoogle Scholar
  23. Jefferies RL, Jensen A, Abraham KF (1979) Vegetational development and the effect of geese on vegetation at La Pérouse Bay, Manitoba. Can J Bot 57:1439–1450CrossRefGoogle Scholar
  24. Jefferies RL, Rockwell RF, Abraham KF (2004) Agricultural food subsidies, migratory connectivity and large-scale disturbance in Arctic coastal systems: a case study. Integr Comp Biol 44:130–139CrossRefPubMedGoogle Scholar
  25. Jefferies RL, Jano AP, Abraham KF (2006) A biotic agent promotes large-scale catastrophic change in the coastal marshes of Hudson Bay. J Ecol 94:234–242CrossRefGoogle Scholar
  26. Korhonen JJ, Soininen J, Hillebrand H (2010) A quantitative analysis of temporal turnover in aquatic species assemblages across ecosystems. Ecology 91:508–517CrossRefPubMedGoogle Scholar
  27. Leafloor JO, Moser TJ, Batt DJ (2012) Evaluation of special management measures for midcontinent lesser snow geese and Ross’s geese. Arctic Goose Joint Venture Special Publication, US Fish and Wildlife Service, Washington, DCGoogle Scholar
  28. MacArthur RH (1965) Patterns of species diversity. Biol Rev 40:510–533CrossRefGoogle Scholar
  29. Maciolek JA (1989) Tundra ponds of the Yukon Delta, Alaska, and their macroinvertebrate communities. In: Vincent WF, Ellis-Evans JC (eds) High latitude limnology. Springer, Dordrecht, pp 193–206CrossRefGoogle Scholar
  30. MacLean SF Jr, Pitelka FA (1971) Seasonal patterns of abundance of tundra arthropods near Barrow. Arctic 24:19–40CrossRefGoogle Scholar
  31. Magurran AE (2007) Species abundance distributions over time. Ecol Lett 10:347–354CrossRefPubMedGoogle Scholar
  32. McLaren JR, Jefferies RL (2004) Initiation and maintenance of vegetation mosaics in an Arctic salt marsh. J Ecol 92:648–660CrossRefGoogle Scholar
  33. Medeiros AS, Quinlan R (2011) The distribution of the Chironomidae (Insecta: Diptera) along multiple environmental gradients in lakes and ponds of the eastern Canadian Arctic. Can J Fish Aquat Sci 68:1511–1527CrossRefGoogle Scholar
  34. Memmott J, Craze PG, Waser NM, Price MV (2007) Global warming and the disruption of plant–pollinator interactions. Ecol Lett 10:710–717CrossRefPubMedGoogle Scholar
  35. Parker BM (1982) Temperature and salinity as factors influencing the size and reproductive potentials of Aedes dorsalis (Diptera: Culicidae). Ann Entomol Soc Am 75:99–102CrossRefGoogle Scholar
  36. Pianka ER (1966) Latitudinal gradients in species diversity: a review of concepts. Am Nat 100:33–46CrossRefGoogle Scholar
  37. Rouse WR, Douglas MS, Hecky RE, Hershey AE, Kling GW, Lesack L, Marsh P, McDonald M, Nicholson BJ, Roulet NT, Smol JP (1997) Effects of climate change on the freshwaters of arctic and subarctic North America. Hydrol Process 11:873–902CrossRefGoogle Scholar
  38. Schneider DW, Frost TM (1996) Habitat duration and community structure in temporary ponds. J North Am Benthol Soc 15:64–86CrossRefGoogle Scholar
  39. Sheath RG (1986) Seasonality of phytoplankton in northern tundra ponds. Hydrobiologia 138:75–83CrossRefGoogle Scholar
  40. Shurin JB (2007) How is diversity related to species turnover through time? Oikos 116:957–965CrossRefGoogle Scholar
  41. Solga MJ, Harmon JP, Ganguli AC (2014) Timing is everything: an overview of phenological changes to plants and their pollinators. Nat Area J 34:227–234CrossRefGoogle Scholar
  42. Srivastava DS, Jefferies RL (1996) A positive feedback: herbivory, plant growth, salinity, and the desertification of an Arctic salt-marsh. J Ecol 84:31–42CrossRefGoogle Scholar
  43. Van Hemert C, Pearce JM, Handel CM (2014) Wildlife health in a rapidly changing North: focus on avian disease. Front Ecol Environ 12:548–556CrossRefGoogle Scholar
  44. Walsh MR, Post DM (2011) Interpopulation variation in a fish predator drives evolutionary divergence in prey in lakes. Proc R Soc B 278:2628–2637CrossRefPubMedPubMedCentralGoogle Scholar
  45. Walsh MR, La Pierre KJ, Post DM (2013) Phytoplankton composition modifies predator-driven life history evolution in Daphnia. Evol Ecol 28:397–411CrossRefGoogle Scholar
  46. Wessel DA, Rouse WR (1994) Modelling evaporation from wetland tundra. Bound Layer Meteorol 68:109–130CrossRefGoogle Scholar
  47. Witter LA, Johnson CJ, Croft B, Gunn A, Poirier LM (2012) Gauging climate change effects at local scales: weather-based indices to monitor insect harassment in caribou. Ecol Appl 22:1838–1851CrossRefPubMedGoogle Scholar
  48. Wolfe BB, Light EM, Macrae ML, Hall RI, Eichel K, Jasechko S, White J, Fishback L, Edwards TW (2011) Divergent hydrological responses to 20th century climate change in shallow tundra ponds, western Hudson Bay Lowlands. Geophys Res Lett 38:L23402Google Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  1. 1.Committee on Evolutionary BiologyUniversity of ChicagoChicagoUSA

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