Altitudinal variation of sexual size dimorphism in ground beetle Carabus odoratus Shill.

Authors

  • Ananina Tatyana State Budgetary Establishment “Zapovednoe Podlemorie”, Komsomolskaya str. 44 – 64, Ulan Ude, 670045, Russian Federation.
  • Sukhodolskaya Raisa State Budgetary Establishment Research Institute for Problems of Ecology and Mineral Wealth, Daurskaya str. 28, Kazan Tatarstan 420087 Russian Federation.
  • Saveliev Anatoliy Kazan (Volga Region), Federal University, Kremlevskaya str. 18, Kazan-2, Tatarstan, Russian Federation.

DOI:

https://doi.org/10.30574/gscbps.2020.12.2.0216

Keywords:

Sexual Size Dimorphism, Ground Beetle, Altitude Gradient, RMA II.

Abstract

Samples of Carabus odoratus barguzinicus Shil. сollected in different altitudes of Barguzin Mountain Range at the northeast part of Baikal Lake (N 54° 20’; E 109° 30’, Russia). In total eight populations were analyzed, two in each belt: Coast, Low-, Middle- and High Mountains (455-460, 500-700, 701-1300, 1301-1700 m above sea level). Morphometric measurements included six traits (elytra length and width, pronotum length and width, head length, and the distance between eyes) of 1300 specimens. Sexual size dimorphism (SSD) in Carabus odoratus was female-biased. Its value was significant and more pronounced in Low- and High mountains and varied from 0.01 to 0.1 in different traits and at different altitudes. The largest values of SSD was at Low- and High mountains. The latter considered the most favorable biotopes to the species studied. RMA II method resulted in positive Intercepts in most traits treated. That demonstrated the higher sensitivity of females to environmental conditions and that Carabus odoratus follows the opposite Rensch′s rule.

Metrics

Metrics Loading ...

References

Darwin C. (1859). On the origin of species. London, Murray, 1-199.

Hedrick AV and Temeles EJ. (1989). Evolution of sexual dimorphism in animals: hypotheses and tests. Trends in Ecology & Evolution, 4(5), 136 – 138.

Honěk A. (1993). Intraspecific variation in body size and fecundity in insects: a general relationship. Oikos, 1, 483 – 492.

Fairbairn DJ. (1997). Allometry for sexual size dimorphism: pattern and process in the coevolution of body size in males and females. Annual review of ecology and systematic, 28(1), 659 – 687.

Temeles EJ, Pan IL, Brennan JL and Horwitt JN. (2000). Evidence for ecological causation of sexual dimorphism in a hummingbird. Science, 289(5478), 441 – 443.

Davidowitz G and Nijhout HF. (2004). The physiological basis of reaction norms: the interaction between growth rate, the duration of growth, and body size. Integrative and Comparative Biology, 44(6), 443 – 449.

Andersson MB. (1994). Sexual selection. Princeton University Press, Princeton, 1-405.

Blanckenhorn WU. (2005). Behavioral causes and consequences of sexual size dimorphism. Ethology, 111(11), 977 – 1016.

Lande R. (1980). Sexual dimorphism, sexual selection, and adaptation in polygenic characters. Evolution, 34(2), 292 – 305.

Slatkin M. (1984). Ecological causes of sexual dimorphism. Evolution, 38(3), 622 – 630.

Shine R. (1989). Ecological causes for the evolution of sexual dimorphism: a review of the evidence. The Quarterly Review of Biology, 64(4), 419 – 461.

Crowley PH. (2000). Sexual dimorphism with female demographic dominance: age, size, and sex ratio at

Savalli UM and Fox CW. (1998). Sexual selection and the fitness consequences of male body size in the seed beetle Statorlimbatus. Animal Behaviour, 55(2), 473 – 483.

Shine R. (1991). Intersexual dietary divergence and the evolution of sexual dimorphism in snakes. The American Naturalist, 138(1), 103 – 122.

Hochkirch A, Gröning J and Krause S. (2007). Intersexual niche segregation in Cepero’s Ground-hopper, Tetrixceperoi. Evolutionary Ecology, 21(6), 727 – 738.

Reeve JP and Fairbairn J. (1999). Change in sexual size dimorphism, as a correlated response to selection on fecundity. Heredity, 83(6), 697 – 706.

Bidau CJ and Marti DA. (2007). Clinal variation of body size in Dichropluspratensis (Orthoptera: Acrididae): inversion of Bergmann's and Rensch's rules. Annals of the Entomological Society of America, 100(6), 850 – 860.

Hochkirch A and Gröning J. (2008). Sexual size dimorphism in Orthoptera (sens. Str.): a review. Journal of Orthoptera Research, 1, 189 – 196.

Kelly CD, Bussière LF and Gwynne DT. (2008). Sexual selection for male mobility in a giant insect with female-biased size dimorphism. The American Naturalist, 172(3), 417 – 423.

Blanckenhorn WU. (2000). The Evolution of body size: what keeps organisms small? The quarterly review of biology, 75(4), 385 – 407.

Wiklund C and Kaitala A. (1995). Sexual selection for large male size in a polyandrous butterfly: the effect of

Bouteiller‐Reuter and Perrin N. (2005). Sex‐specific selective pressures on body mass in the greater white‐toothed shrew, Crocidura russula. Journal of evolutionary biology, 18(2), 290 – 300.

Cox RM and Calsbeek R. (2010). Sex‐specific selection and intraspecific variation in sexual size dimorphism. Evolution: International Journal of Organic Evolution, 64(3), 798 – 809.

Stillwell RC, Blanckenhorn WU, Teder T, Davidowitz G and Fox CW. (2010). Sex differences in phenotypic plasticity affect variation in sexual size dimorphism in insects: from physiology to evolution. Annual review of entomology, 55, 227 – 245.

Atkinson D. (1994). Temperature and organism size: a biological law for ectotherms? Adv. Ecol. Res, 25, 1 – 58.

Angilletta MJ and Dunham AE. (2003). The Temperature-size rule in ectotherms: simple evolutionary explanations may not be general. The American Naturalist, 162(3), 332 – 342.

Teder T and Tammaru T. (2005). Sexual size dimorphism with in species increases with body size in insects. Oikos, 108(2), 321 – 334.

Abouheif E and Fairbairn DJ. (1997). Comparative analysis of allometry for sexual size dimorphism: assessing Rensch's rule. The American Naturalist, 149(3), 540 – 562.

Rensch BE. (1950). Die Abhängigkeit der relative en Sexual differenz vonde rKörpergrösse. Bonner Zoologische Beiträge, 1, 58 – 69.

Blanckenhorn WU, Dixon AF, Fairbairn DJ, Foellmer MW, Gibert P, Linde KV, Meier R, Nylin S, Pitnick S, Schoff C and Signorelli M. (2006). Proximate causes of Rensch’s rule: does sexual size dimorphism in arthropods result from sex differences in development time? The American Naturalist, 169(2), 245 – 257.

Fairbairn DJ, Blanckenhorn WU and Székely T. (2007). Sex, size, and gender roles: Evolutionary studies of sexual size dimorphism. Oxford University Press, Oxford, UK, 1-290.

Kraushaar U and Blanckenhorn WU. (2002). Population variation in sexual selection and its effect on size allometry in two dung fly species with contrasting sexual size dimorphism. Evolution, 56(2), 307 – 321.

Quezada‐Euán JJ, Sanabria‐Urbán S, Smith C and Cuevadel-Castillo R. (2019). Patterns of sexual size dimorphism in stingless bees: Testing Rensch’s rule and potential causes in highly eusocial bees (Hymenoptera: Apidae, Meliponini). Ecology and evolution, 9(5), 2688 – 2698.

Ananin АА and Ananina Т L. (2011). Long-term dynamics of birds and ground beetles population density in catena of Barguzinskiy ridge (Northern Pribaikalye). Findings of Samara Research Centre of Russian Academy of Sciences, 13(1/5), 1041-1044.

Ananina ТL. (2010). Carabid’s dynamic of number in Mountain of North-East Prybaikalie. State nature biosphere reserve “Barguzinskyi”. Buryat State University Publishing Department, Ulan-Ude, 1- 120.

Obydov D. (2006). A new subspecies of Carabus (Morphocarabus) odoratusMotchulsky, 1844 (Coleoptera, Carabidae) from Eastern Siberia. Mun. Entom. Zoology, 1(1), 149.

Shilenkov VG. (1996). Ground Beetles of Carabus L. genus of Southern Siberia. Irkutsk University Publishing, Irkutsk, 1-88.

Lovich JE and Gibbons JW. (1992). A review of techniques for quantifying sexual size dimorphism. Growth Development and Aging, 56, 269 – 281.

R Development Team. (2015). R: A Language and environment for statistical computing. Vienna, Austria, 1- 409.

Fairbairn DJ and Preziosi RF. (1994). Sexual selection and the evolution of allometry for sexual size dimorphism in the water strider, Aquarius remigis. The American Naturalist, 144(1), 101 – 118.

Fairbairn DJ. (2005). Allometry for sexual size dimorphism: testing two hypotheses for Rensch’s rule in the water strider Aquarius remigis. The American Naturalist, 166(4), 69 – 84.

Young KA. (2005). Life–history variation and allometry for sexual size dimorphism in Pacific salmon and trout. Proceedings of the Royal Society B. Biological Sciences, 272(1559), 167 – 172.

Sukhodolskaya RA, Saveliev AA and Muhammetnabiev TR. (2016). Sexual Dimorphism of Insects and Conditions of Its Manifestation. Research Journal of Pharmaceutical, Biological and Chemical Sciences, 7(2), 1992 – 2001.

Ananina TL. (2015). Biotopic preferences of ground beetles (Carabidae, Coleoptera) of the Barguzin Ridge by the example of Carabus odoratus barguzinicus Shil. Eurasian Entomological Journal, 14(6), 511-517.

Sukhodolskaya RA and Ananina TL. (2015). Altitudinal variation in population density, body size and morphometric structure in Carabus odoratus Shil, 1996 (Coleoptera: Carabidae). Acta Biol. Univ. Daugavp, 15(1), 179 – 190.

Ikeda H, Tsuchiya Y, Nagata N, Ito MT and Sota T. (2012). Altitudinal life cycle and body-size variation in ground beetles of the genus Carabus (subgenus Ohomopterus) in relation to the temperature conditions and prey earthworms. Pedobiologia, 55(2), 67 – 73.

Cvetkovska-Gjorgjievska A, Hristovski S, Prelić D, Jelaska LŠ, Slavevska-Stamenković V and Ristovska M. (2017). Body size and mean individual biomass variation of ground-beetles community (Coleoptera: Carabidae) as a response to increasing altitude and associated vegetation types in mountainous ecosystem. Biologia, 72(9), 1059 – 1066.

Brehm G, Zeuss D and Colwell RK. (2018). Moth body size increases with elevation along a complete tropical elevational gradient for two hyper diverse clades. Ecography, 41, 1 – 11.

Baranovská E and Knapp M. (2018). Steep converse Bergmann's cline in a carrion beetle: between‐and within‐population variation in body size along an elevational gradient. Journal of Zoology, 304(4), 243 – 251.

Bulgarella M, Trewick SA, Godfrey AJ, Sinclair BJ and Morgan-Richards M. (2015). Elevational variation in adult body size and growth rate but not in metabolic rate in the tree weta Hemideina crassidens. Journal of insect physiology, 75, 30 – 38.

Downloads

Published

2022-02-04

How to Cite

Tatyana , A., Raisa , S., & Anatoliy, . S. (2022). Altitudinal variation of sexual size dimorphism in ground beetle Carabus odoratus Shill. GSC Biological and Pharmaceutical Sciences, 12(2), 027–036. https://doi.org/10.30574/gscbps.2020.12.2.0216

Issue

Section

Review Article