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Variation of hind-wing colour and length in Sympetrum internum (Odonata: Libellulidae) from the Canadian prairie provinces

Published online by Cambridge University Press:  02 April 2012

Paul M. Catling
Affiliation:
Biodiversity, National Program on Environmental Health, Research Branch, Agriculture and Agri-Food Canada, William Saunders Building, Central Experimental Farm, Ottawa, Ontario, Canada K1A 0C6 (e-mail: catlingp@agr.gc.ca)

Abstract

Amber coloration, called saffroning, extends from 1 to 15 mm across the hind-wing base in females of Sympetrum internum Montgomery from the prairie provinces but extends only from 2 to 3 mm in males. There are no substantial differences in hind-wing length between the sexes. A significant correlation was found between hind-wing length and the extent of saffroning for both males and females. Regressions of these characters against latitude and longitude revealed that (1) there is a significant decrease in hind-wing length northward for both sexes; (2) there is a significant decrease in saffroning northward that is more significant for females; (3) there is no significant effect of longitude on hind-wing length; and (4) saffroning in females significantly increases westward but there is no similar effect in males, and the trend in females is much less significant than the latitudinal trend. Within the prairie provinces, extensive saffroning is confined to the Prairie Ecozone and moderate saffroning occurs around the edges of this ecozone. The surrounding Boreal Plains Ecozone is characterized by females with very limited saffroning. There is generally extensive variation in the extent of saffroning within some Prairie Ecozone locations, ranging from limited to moderate or extensive, but limited and moderate saffroning were more frequent at most locations in the Prairie Ecozone. Various explanations for saffroning are considered. Since limited, moderate, and extensive saffroning occur together throughout an extensive area, and occur within many populations and within a group emerging at the same time, formal taxonomic recognition of individuals with moderate or extensive saffroning seems unwarranted.

Résumé

Une coloration ambrée, appelée ici safranisation, s’étend sur une distance de 1 à 15 mm à la base de l’aile postérieure des femelles de Sympetrum internum Montgomery des provinces des Prairies, mais seulement sur 2 à 3 mm chez les mâles. Il n’y a pas de différence importante de longueur de l’aile postérieure entre les deux sexes. Il existe une corrélation significative entre la longueur de l’aile et l’étendue de la safranisation, tant chez les mâles que les femelles. Des régressions de ces caractères en fonction de la latitude et la longitude montrent: (1) une diminution significative de la longueur de l’aile vers le nord chez les deux sexes, (2) une diminution significative de la safranisation vers le nord, plus marquée chez les femelles, (3) aucun effet significatif de la longitude sur la longueur de l’aile postérieure et (4) une augmentation significative de la safranisation en direction ouest, chez les femelles, mais nullement chez les mâles; cette tendance chez les femelles est beaucoup moins significative que la tendance latitudinale. Dans les provinces des Prairies, la safranisation étendue est confinée à l’écozone des Prairies avec une safranisation modérée en périphérie de l’écozone. Les femelles de l’écozone environnante des Plaines boréales se caractérisent par une safranisation très réduite. Il y a généralement une importante variation de l’étendue de la safranisation dans quelques localités de l’écozone des Prairies, allant de réduite à modérée et à importante; la safranisation réduite ou modérée est la plus commune dans la plupart des localités de l’écozone des Prairies. Plusieurs explications de la safranisation sont considérées. Puisque des safranisations réduites, modérées et importantes peuvent se retrouver ensemble sur une grande étendue géographique et qu’elles peuvent survenir au sein de plusieurs populations et dans un groupe qui émerge ensemble à la même période, il n’est pas justifié de reconnaître taxonomiquement les individus qui possèdent une safranisation modérée ou importante.

[Traduit par la Rédaction]

Type
Articles
Copyright
Copyright © Entomological Society of Canada 2007

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References

Cannings, R.A. 1980. Ecological notes on Sympetrum madidum (Hagen) in British Columbia, Canada (Anisoptera: Libellulidae). Notulae Odonatologicae, 1 (6): 9799.Google Scholar
Cannings, R.A. 2002. Introducing the dragonflies of British Columbia. Royal British Columbia Museum, Victoria, British Columbia.Google Scholar
Cannings, R.A., and Stuart, K.M. 1977. The dragon-flies of British Columbia. British Columbia Provincial Museum Handbook No. 35.Google Scholar
Cannings, S.G., and Cannings, R.A. 1997. Dragon-flies (Odonata) of the Yukon. In Insects of the Yukon. Edited by Danks, H.V. and Downes, J.A.. Biological Survey of Canada (Terrestrial Arthropods), Ottawa, Ontario. pp. 169200.Google Scholar
Carle, F.L. 1993. Sympetrum janeae spec. nov. from eastern North America, with a key to the Nearctic Sympetrum (Anisoptera: Libellulidae). Odonatologica, 22 (1): 116.Google Scholar
Catling, P.M., Cannings, R.A., and Brunelle, P.M. 2005. An annotated checklist of the Odonata of Canada. Bulletin of American Odonatology, 9 (1): 120.Google Scholar
Corbet, P.S. 1999. Dragonflies — behaviour and ecology of Odonata. Cornell University Press, Ithaca, New York.Google Scholar
Donnelly, T.W. 1991. Current problems in Sympetrum and Libellula (a.k.a. Plathemis). Argia (Newsjournal of the Dragonfly Society of the Americas), 3 (4): 812.Google Scholar
Donnelly, T.W. 2004. Distribution of North American Odonata. Part II: Macromiidae, Corduliidae and Libellulidae. Bulletin of American Odonatology, 8 (1): 132.Google Scholar
Dunkle, S.W. 2000. Dragonflies through binoculars — a field guide to dragonflies of North America. Oxford University Press, New York.Google Scholar
Frantsevich, L.I., and Mokrushov, P.A. 1984. Visual stimuli releasing attack of a territorial male in Sympetrum (Anisoptera: Libellulidae). Odonatologica, 13: 335350.Google Scholar
Gardner, A.E. 1951. The life-history of Sympetrum danae (Sülzer) = S. scoticum (Donovan) (Odonata). Entomologist's Gazette, 2: 109127.Google Scholar
Johansson, F., Crowley, P.H., and Brodin, T. 2005. Sexual size dimorphism and sex ratios in dragonflies (Odonata). Biological Journal of the Linnaean Society, 86 (4): 507513.CrossRefGoogle Scholar
Miller, L.A., Hamrun, C.L., and Anderson, M.A. 1964. Identification and distribution of Sympetrum in Minnesota (Libellulidae, Odonata). Proceedings of the Minnesota Academy of Science, 31 (2): 116119.Google Scholar
Montgomery, B.E. 1943. Sympetrum internum, new name for Sympetrum decisum auct., nec Hagen, Odonata, Libellulidae. The Canadian Entomologist, 75: 5758.CrossRefGoogle Scholar
Needham, J.G., Westfall, M.J. Jr., and May, M.L. 2000. Dragonflies of North America. Scientific Publishers, Gainesville, Florida.Google Scholar
Tai, L.C.C. 1967. Biosystematic study of Sympetrum (Odonata: Libellulidae). Ph.D. thesis, Purdue University, Lafayette, Indiana.Google Scholar
Tillyard, R.J. 1917. The biology of dragonflies. Cambridge University Press, Cambridge, United Kingdom.Google Scholar
Van Buskirk, J. 1987. Influence of size and date of emergence on male survival and mating success in a dragonfly, Sympetrum rubicundulum. American Midland Naturalist, 118 (1): 169176.CrossRefGoogle Scholar
Walker, E.M. 1912. The Odonata of the prairie provinces of Canada. The Canadian Entomologist, 44 (9): 253266.CrossRefGoogle Scholar
Walker, E.M. 1927. The Odonata of the Canadian Cordillera. Provincial Museum of Natural History of British Columbia, Victoria, British Columbia.Google Scholar
Walker, E.M. 1938. Notes on Odonata from the vicinity of Cultus Lake, B.C. The Canadian Entomologist, 70 (7): 144151.CrossRefGoogle Scholar
Walker, E.M. 1940. A preliminary list of the Odonata of Saskatchewan. The Canadian Entomologist, 72 (2): 2635.CrossRefGoogle Scholar
Walker, E.M. 1947. Further notes on the subarctic Odonata of North America. The Canadian Entomologist, 79 (4): 6267.CrossRefGoogle Scholar
Walker, E.M. 1950. Notes on some Odonata from Kenora and Rainy River Districts, Ontario. The Canadian Entomologist, 82 (1): 1621.CrossRefGoogle Scholar
Walker, E.M. 1951 a. Sympetrum semicinctum and its allies. Entomological News, 62 (5): 153163.Google Scholar
Walker, E.M. 1951 b. The Odonata of the northern insect survey. The Canadian Entomologist, 83 (10): 269278.CrossRefGoogle Scholar
Walker, E.M., and Corbet, P.S. 1975. The Odonata of Canada and Alaska. Vol. 3. Part III: The Anisoptera — three families. University of Toronto Press, Toronto, Ontario.CrossRefGoogle Scholar
Whitehouse, F.C. 1941. British Columbia dragonflies (Odonata), with notes on distribution and habits. American Midland Naturalist, 26 (3): 488557.CrossRefGoogle Scholar
Williamson, E.B. 1933. The status of Sympetrum assimilatum (Uhler) and Sympetrum decisum (Hagen). (Odonata—Libelulinae). Occasional Papers of the Museum of Zoology, University of Michigan No. 264. pp. 17.Google Scholar
Wissinger, S.A. 1988. Spatial distribution life history and estimates of survivorship in a fourteen-species assemblage of larval dragonflies (Odonata: Anisoptera). Freshwater Biology, 20 (30): 329340.CrossRefGoogle Scholar