Abstract
The winter dormancy adaptation in gall-inducing sawflies is poorly known. Diapause termination and the following post-diapause quiescence enhance synchronous eclosion in spring. This is probably the most critical part in the life history in gall-inducing sawflies, as there is only a short phenological window of opportunity for mating and oviposition. In a 2 years’ study, diapause duration, termination, survival and eclosion synchrony were experimentally investigated for three gall-inducing sawfly species (Symphyta: Tenthredinidae: Pontania nivalis, P. glabrifrons and P. arcticornis). Field-collected galls, sampled from willows (Salix spp.) in early autumn, were kept under natural temperatures outdoors until next spring. Subsamples were successively transferred to the laboratory at 14-day intervals from October to April in a test of development time to eclosion and survival ratio. The time to eclosion decreased throughout the experiment, whereas the proportion successfully eclosed and eclosion synchronicity increased, all indicative of prepupae entering a diapause in early autumn. The diapause terminates midwinter, and the prepupae enter a post-diapause quiescence until the temperature in spring allows a direct development and contributes to a nearly synchronous eclosion. In all three species, males eclosed 1–2 days prior to females (protandry). We hypothesize that synchronous eclosion as well as protandry enhance mating and oviposition success. Our finding indicates that gall-inducing sawflies are well adapted to its harsh subarctic and arctic environment.
Similar content being viewed by others
References
Bartelt RJ, Kulman HM, Jones RL (1981) Effect of temperature on diapausing cocoons of the yellowheaded spruce sawfly, Pikonema alaskensis. Ann Entomol Soc Am 72:472–477
Craig TP, Mopper S (1993) Sex ratio variation in sawflies. In: Wagner MR, Raffa KF (eds) Sawfly life history adaptation to woody plants. Academic Press, San Diego, pp 61–92
Craig TP, Price PW, Itami JK (1992) Facultative sex ratio shifts by a herbivorous insect in response to variation in host plant quality. Oecologia 92:153–161
Danks HV (1987) Insect dormancy: an ecological perspective. Biol Survey Canada, Natl Mus Nat Sci, Ottawa
Danks HV (2004) Seasonal adaptations in arctic insects. Integr Comp Biol 94:85–94
Denlinger DL (2002) Regulation of diapause. Annu Rev Entomol 47:93–122
Elverum F, Johansen TJ, Nilssen AC (2003) Life history, egg cold hardiness and diapause of Argyresthia retinella (Lepidoptera: Yponomeutidae). Nor J Entomol 50:43–53
Fagerström T, Wiklund C (1982) Why do males emerge before females? Protandry as a mating strategy in male and female butterflies. Oecologia 54:164–166
Graf B, Höhn H, Höpli HU (1996) The apple sawfly, Hoplocampa testudinea: a temperature driven model for spring emergence of adults. Entomol Exp Appl 78:301–307
Henden JA, Ims RA, Yoccoz NG, Sørensen R, Killengreen ST (2011) Population dynamics of tundra voles in relation to configuration of willow thickets in southern arctic tundra. Polar Biol 34:533–540
Hjältén J, Roininen H, Danell K, Price PW (2003) Distribution and oviposition preference of galling sawflies in arctic Canada. Polar Biol 26:768–773
Hodek I (1988) Photoperiodic response and reproductive activity in Pyrrhocoris-Apterus L. (Heteroptera) in relation to diapause development. Zool Jahrb Allg Zool 92:57–70
Hodek I (1996) Diapause development, diapause termination and the end of diapause. Eur J Entomol 93:475–487
Hodek I (2002) Controversial aspects of diapause development. Eur J Entomol 99:163–173
Hodek I, Hodková M (1988) Multiple role of temperature during insect diapause: a review. Entomol Exp Appl 49:153–165
Humble LM (2006) Overwinter adaptation in arctic sawflies (Hymenoptera: Tenthredinidae) and their parasitoids: cold tolerance. Can Entomol 138:59–71
Kalushkov P, Hodková M, Nedvěd O, Hodek I (2001) Effect of thermoperiod on diapause intensity in Pyrrhocoris apterus (Heteroptera Pyrrhocoridae). J Insect Physiol 47:55–61
Karlsen SR, Høgda KA, Johansen B, Elvebakk A, Tømmervik H (2002) Use of AVHRR NDVI data to map vegetation zones in north-western Europe. In: Proceeding of the 29th international symposium on remote sensing of environment (ISRSE), Buenos Aires, p 4
Knerer G (1983) Diapause strategies in Diprionid sawflies. Naturwissenschaften 70:203–205
Knerer G (1993) Life history diversity in sawflies. In: Wagner MR, Raffa KF (eds) Sawfly life history adaption to woody plants. Academic Press, San Diego, pp 33–59
Kopelke J-P (1990) Die Arten der viminalis-Gruppe, Gattung Pontania O. Costa 1859, Mittel- und Nordeuropas (Insecta: Hymenoptera: Tenthredinidae). Senckenb Biol 71:65–128
Kopelke J-P (1999) Gallenerzeugende Blattwepsen Europas—Taxonomiche Grundlagen, Biologie und Ökologie (Tenthredinidae: Nematinae: Euura, Phyllocolpa, Pontania). Cour Forschungsinst Senckenb 212:1–183
Koštál V (2006) Eco-physiological phases of insect diapause. J Insect Physiol 52:113–127
Martel J, Kause A (2002) The phenological window of opportunity for early-season birch sawflies. Ecol Entomol 27:302–307
Masaki S (2002) Ecophysiological consequences of variability in diapause intensity. Eur J Entomol 99:143–154
Moen A (1999) Natsjonalatlas for Norge: Vegetasjon. Statens kartverk, Norwegian Mapping Authority, Hønefoss
Morbey YE, Ydenberg RC (2001) Protandrous arrival timing to breeding areas: a review. Ecol Lett 4:663–673
Nilssen A, Tenow O (1990) Diapause, embryo growth and supercooling capacity of Epirrita autumnata eggs from northern Fennoscandia. Entomol Exp Appl 57:39–55
Nunes MV, Saunders D (1999) Photoperiodic time measurement in insects: a review of clock models. J Biol Rhythms 14:84–104
Nuorteva M (1971) Die Sägewepsenfauna (Hym., Symphyta) von Vuohiniem, Südfinnland. Ann Ent Fenn 37:179–189
Nyman T, Farrell BD, Zinovjev AG, Vikberg V (2006) Larval habits, host-plant associations, and speciation in nematine sawflies (Hymenoptera: Tenthredinidae). Evolution 60:1622–1637
Price PW (2003) Macroevolutionary theory on macroevolutionary patterns. Cambridge University Press, New York
Price P, Roininen H, Zinovjev AG (1998) Adaptive radiation of gall-inducing sawflies in relation to architecture and geographic range of willow host plants. In: Csóka G, Matteson WJ, Stone GN, Price PW (eds) The biology of gall-inducing arthropods. USDA Forest Service Gen Tech Rep NC-199, pp 196–203
Ring RA, Tesar D (1981) Adaption to cold in Canadian arctic insects. Cryobiology 18:199–211
Roininen H, Danell K, Zinovjev A, Vikberg V, Virtanen R (2002) Community structure, survival and mortality factors in arctic populations of Eupontania leaf gallers. Polar Biol 25:605–611
Saunders DS (2002) Insect clocks, 3rd edn. Elsevier, Amsterdam
Tanno K (1970) Frost injury and resistance in the poplar sawfly, Trichiocampus populi Okamoto. Contrib Inst Low Temp Sci Hokkaido Univ B 16:1–41
Tauber MJ, Tauber CA (1976) Insect seasonality: diapause maintenance, termination, and postdiapause development. Annu Rev Entomol 21:81–107
Tauber MJ, Tauber CA, Masaki S (1986) Seasonal adaptation of insects. Oxford University Press, New York
Uchidoi T, Naito T, Takeda M (1993) Life cycle characteristics of sympatric Athalia sawflies (Hymenoptera: Tenthredinidae) sharing food resources. Appl Entomol Zool 28:407–415
Viitasaari M (2002) Sawflies (Hymenoptera, Symphyta) Vol I: a review of the suborder, the Western Palearctic taxa of Xyeloidae and Pamphilioidae. Tremex Press Ltd, Helsinki
Virtanen R, Oksanen L, Razzhivin V (1999) Topographical and regional patterns of tundra heath vegetation from northern Fennoscandia to the Taimyr Peninsula. Acta Bot Fenn 167:29–83
Wagner MR, Raffa KF (1993) Sawfly life history adaptations to woody plants. Academic Press Inc, San Diego
Walker DA, Raynolds MK, Daniels FJA, Einarsson E, Elvebakk A, Gould WA, Katenin AE, Kholod SS, Markon CJ, Melnikov ES, Moskalenko NG, Talbot SS, Yurtsev BA (2005) The circumpolar Arctic vegetation map. J Veg Sci 16:267–282
Wiklund C, Fagerström T (1977) Why do males emerge before females? A hypothesis to explain the incidence of protandry in butterflies. Oecologia 31:153–158
Zinovjev AG (1998) Palearctic sawflies of the genus Pontania Costa (Hymeoptera: Tenthredinidae) and their host-plant specificity. In: Csóka G, Matteson WJ, Stone GN, Price PW (eds) Biology of gall-inducing arthropods. USDA Forest Service Gen Tech Rep NC-199, pp 204–225
Acknowledgments
We would like to thank the “EcoFinn” project at University of Tromsø for help with field logistics and accommodation, Terje Barstad as field assistant and Prof. John R. Anderson for improving the language. The study was funded by Tromsø University Museum.
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Barstad, T.E., Nilssen, A.C. Hibernation adaptation and eclosion synchrony in leaf-galling sawflies in subarctic Norway. Polar Biol 35, 1097–1103 (2012). https://doi.org/10.1007/s00300-012-1157-8
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00300-012-1157-8