Increase in dark morphs and decrease in size during a range extension of Cheilomenes sexmaculata (coleoptera: coccinellidae)

The ladybird beetle Cheilomenes sexmaculata (Fabricius) is widely distributed throughout the intermediate latitudinal and equatorial regions. It exhibits elytral colour polymorphism with a geographical cline showing increased prevalence of melanic morphs with increasing latitude. Over the past 100 years, this species has extended its distribution towards higher latitudes in Japan because of climatic warming. In this study, long-term changes in the frequency of different morphs and adult body size of this species during this range extension were analyzed based on a survey of specimens in collections. First, we examined specimens collected from areas that were colonized (34-36°N) during the period of range extension (1949-1989) and when it ceased (1990-2005). Chronologically, both the proportions of melanic morphs increased and body size decreased significantly. Next, specimens were examined from newly colonized regions and the former range of distribution (32-34°N); these specimens were collected during period when range extension had ceased. In newly colonized regions, the frequency of melanic morphs was higher and the body size was smaller than in the former range of distribution. These two findings indicate that the smaller, melanic morphs may have undergone a positive-selection driven range extension to higher latitudes.

[1]  K. Yamazaki,et al.  Northward expansion and climatic factors affecting the distribution limits of Cheilomenes sexmaculata (Coleoptera: Coccinellidae) in Japan , 2013, Applied Entomology and Zoology.

[2]  K. Yamazaki,et al.  Geographical variations of elytral color polymorphism in Cheilomenes sexmaculata (Fabricius) (Coleoptera: Coccinellidae) , 2013 .

[3]  A. Dixon,et al.  Temporal variation in elytral colour polymorphism in Hippodamia variegata (Coleoptera: Coccinellidae) , 2012 .

[4]  I. Hodek,et al.  Ecology and behaviour of the ladybird beetles (Coccinellidae) , 2012 .

[5]  A. Roques,et al.  Direct impacts of recent climate warming on insect populations. , 2010, Integrative zoology.

[6]  A. Honěk Factors affecting the distribution of larvae of aphid predators (Col., Coccinellidae and Dipt., Syrphidae) in cereal stands , 2009 .

[7]  D. Musolin,et al.  Some like it hot! Rapid climate change promotes changes in distribution ranges of Nezara viridula and Nezara antennata in Japan , 2009 .

[8]  S. Boman Ecological and genetic factors contributing to invasion success : the northern spread of the Colorado potato beetle (Leptinotarsa decemlineata) , 2008 .

[9]  J. Yukawa,et al.  Distribution range shift of two allied species, Nezara viridula and N. antennata(Hemiptera: Pentatomidae), in Japan, possibly due to global warming , 2007 .

[10]  D. Musolin Insects in a warmer world: ecological, physiological and life‐history responses of true bugs (Heteroptera) to climate change , 2007 .

[11]  C. Fox,et al.  Geographic Variation in Body Size and Sexual Size Dimorphism of a Seed‐Feeding Beetle , 2007, The American Naturalist.

[12]  W. Blanckenhorn,et al.  Bergmann and Converse Bergmann Latitudinal Clines in Arthropods: Two Ends of a Continuum?1 , 2004, Integrative and comparative biology.

[13]  L. Kang,et al.  Variation in Cold Hardiness of Liriomyza huidobrensis (Diptera: Agromyzidae) Along Latitudinal Gradients , 2004 .

[14]  H. Strouhal Variationsstatistische untersuchung an adonia variegata gze. (col. coccinell.) , 1939, Zeitschrift für Morphologie und Ökologie der Tiere.

[15]  J. Régnière,et al.  Assessing the Impacts of Global Warming on Forest Pest Dynamics , 2022 .

[16]  Robert D. Holt,et al.  On the evolutionary ecology of species' ranges , 2003 .

[17]  Masanobu. Yoshio,et al.  Relationship between cold hardiness and northward invasion in the great mormon butterfly, Papilio memnon L. (Lepidoptera: Papilionidae) in Japan , 2001 .

[18]  Sam P. Brown,et al.  Autumn tree colours as a handicap signal , 2001, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[19]  A. Yediler,et al.  [Transportation and transformation of 14C-phenanthrene in closed chamber (nutrient solution-lava-plant-air) system]. , 2001, Ying yong sheng tai xue bao = The journal of applied ecology.

[20]  R. Ishikawa,et al.  Geographic Variation in the Body Size of Some Japanese Leptocarabus Species (Coleoptera, Carabidae) : The "Toppled-Domino Pattern" in Species along a Geographic Cline , 2000 .

[21]  D. Roff,et al.  THE EVOLUTIONARY GENETICS OF AN ADAPTIVE MATERNAL EFFECT: EGG SIZE PLASTICITY IN A SEED BEETLE , 1999, Evolution; international journal of organic evolution.

[22]  H. Takada,et al.  Suitability of Seven Aphid Species as Prey of Cheilomenes sexmaculata (Fabricius) (Coleoptera: Coccinellidae). , 1998 .

[23]  I. Hodek,et al.  Effect of Temperature on Pupal Pigmentation and Size of the Elytral Spots in Coccinella septempunctata (Coleoptera: Coccinellidae) from Four Latitudes in Japan , 1997 .

[24]  T. Gomi Geographic variation in critical photoperiod for diapause induction and its temperature dependence in Hyphantria cunea Drury (Lepidoptera: Arctiidae) , 1997, Oecologia.

[25]  A. J. Moore,et al.  The genetics of phenotypic plasticity in a colonizing population of the ladybird beetle, Hormonia axyridis , 1997, Heredity.

[26]  A. Honěk Life History and Development , 1996 .

[27]  J. Obrycki,et al.  Thermal and Dietary Requirements for Development of Hippodamia parenthesis (Coleoptera: Coccinellidae) , 1990 .

[28]  J. Obrycki,et al.  Suitability of Three Prey Species for Nearctic Populations of Coccinella septempunctata, Hippodamia variegata, and Propylea quatuordecimpunctata (Coleoptera: Coccinellidae) , 1990 .

[29]  A. Dixon,et al.  Why big species of ladybird beetles are not melanic , 1989 .

[30]  A. Dixon,et al.  Why There are So Few Species of Aphids, Especially in the Tropics , 1987, The American Naturalist.

[31]  H. Danks Insect dormancy: an ecological perspective. , 1987 .

[32]  P. Brakefield,et al.  The basis of thermal melanism in the ladybird Adalia bipunctata: Differences in reflectance and thermal properties between the morphs , 1985, Heredity.

[33]  C. N. Slobodchikoff,et al.  A New Ecology: Novel Approaches to Interactive Systems , 1984 .

[34]  H. Sasaji,et al.  Reproductive Continuity and Genetic Relationships in the Forms of the Genus Menochilus(Coleoptera:Coccinellidae) , 1979 .

[35]  D. Lonsdale,et al.  Is polymorphism in two-spot ladybird an example of non-industrial melanism? , 1974, Nature.

[36]  Sinzo Masaki GEOGRAPHIC VARIATION AND CLIMATIC ADAPTATION IN A FIELD CRICKET (ORTHOPTERA: GRYLLIDAE) , 1967, Evolution; international journal of organic evolution.

[37]  R. Blackman Studies on specificity in Coccinellidae , 1965 .

[38]  A. S. Danilevskiĭ Photoperiodism and seasonal development of insects , 1965 .

[39]  T. Dobzhansky Geographical Variation in Lady-Beetles , 1933, The American Naturalist.