Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-19T04:17:12.214Z Has data issue: false hasContentIssue false

Seasonal abundance and prey selection of the nymphs of three sympatric species of Sympetrum (Odonata: Libellulidae) in an intermittent pond

Published online by Cambridge University Press:  02 April 2012

Catherine M. Febria
Affiliation:
Surface and Groundwater Ecology Research Group, Department of Life Sciences, University of Toronto at Scarborough, Ontario, Canada M1C 1A4
A. Katarina Magnusson
Affiliation:
Surface and Groundwater Ecology Research Group, Department of Life Sciences, University of Toronto at Scarborough, Ontario, Canada M1C 1A4
D. Dudley Williams*
Affiliation:
Surface and Groundwater Ecology Research Group, Department of Life Sciences, University of Toronto at Scarborough, Ontario, Canada M1C 1A4
*
1 Corresponding author (e-mail: [email protected]).

Extract

Odonates are obligate predators (Pritchard 1964), and the composition of their diet is reflective of their microhabitat and effectiveness in detecting and capturing prey (Griffiths 1973; Thompson 1978). In an intermittent woodland pond in southern Ontario, Canada, three species of Sympetrum (Odonata: Libellulidae) were found to coexist: S. internum Montgomery, S. costiferum (Hagen), and S. obtrusum (Hagen). Sympetrum species spend most of their life cycle in the aquatic stage and consume prey at all nymphal stadia (Pritchard 1964; Corbet 1999). They overwinter in the egg stage, hatch in early spring, and typically emerge in late June to late July (Walker and Corbet 1975). To better understand the role of coexisting Sympetrum nymphs in this intermittent pond environment, and to evaluate potential mechanisms behind their coexistence, we collected seasonal abundance and body size data for 2 years and analyzed gut contents of each species. In addition, we experimentally tested the prey selection and predatory rate of two different size classes of Sympetrum nymphs and two of their potential competitors, Lestes sp. (Odonata: Lestidae) and Acilius sp. (Coleoptera: Dytiscidae), in laboratory microcosms.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 2005

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.)

References

Bazzanti, M., Della Bella, V., and Seminara, M. 2003. Factors affecting macroinvertebrate communities in astatic ponds in central Italy. Journal of Freshwater Ecology, 18: 537548.Google Scholar
Benke, A.C., and Benke, S.S. 1975. Comparative dynamics and life histories of coexisting dragonfly populations. Ecology, 56: 302317.CrossRefGoogle Scholar
Corbet, P.S. 1999. Dragonflies: behaviour and ecology of Odonata. Cornell University Press, Ithaca, New York.Google Scholar
Griffiths, D. 1982. The food of animals in an acid moorland pond. Journal of Animal Ecology, 42: 285293.Google Scholar
Havel, J.E., Link, J., and Niedzwiecki, J. 1993. Selective predation by Lestes (Odonata, Lestidae) on littoral microcrustacea. Freshwater Biology, 29: 4758.Google Scholar
Johnson, D.M., Crowley, P.H., Bohanan, R.E., Watson, C.N., and Martin, T.H. 1985. Competition among larval dragonflies — a field enclosure experiment. Ecology, 66: 119128.CrossRefGoogle Scholar
Larson, D.J. 1990. Odonate predation as a factor influencing dytiscid beetle distribution and community structure. Quaestiones Entomologicae, 26: 151162.Google Scholar
Merrit, R.W., and Cummins, K.W. 1984. An introduction to the aquatic insects of North America. 2nd ed. Kendall/Hunt, Dubuque, Iowa.Google Scholar
Pritchard, G. 1964. Prey of dragonfly larvae (Odonata; Anisoptera) in ponds in northern Alberta. Canadian Journal of Zoology, 42: 785800.CrossRefGoogle Scholar
Schneider, D.W., and Frost, T.M. 1996. Habitat duration and community structure in temporary ponds. Journal of the North American Benthological Society, 15: 6486.CrossRefGoogle Scholar
Tavares-Cromar, A.F., and Williams, D.D. 1996. The importance of temporal resolution in food web analysis: evidence from a detritus-based system. Ecological Monographs, 66: 91113.CrossRefGoogle Scholar
Thompson, D.J. 1978. Prey selection by larvae of the damselfly, Ischnura elegans (Odonata). Journal of Animal Ecology, 47: 769785.CrossRefGoogle Scholar
Thorp, J.H., and Cothran, M.L. 1984. Regulation of freshwater community structure at multiple intensities of dragonfly predation. Ecology, 65: 15461555.CrossRefGoogle Scholar
Walker, E.M., and Corbet, P. S. 1975. The Odonata of Canada and Alaska. Vol. 3. The Anisoptera — three families. University of Toronto Press, Toronto, Ontario.Google Scholar
Williams, D.D. 2005. The biology of temporary waters. Oxford University Press, Oxford.CrossRefGoogle Scholar
Wissinger, S.A. 1988. Life history and size structure of larval dragonfly populations. Journal of the North American Benthological Society, 7(1): 1328.Google Scholar