Transgenerational effects on overall fitness: influence of larval feeding experience on the oviposition behaviour of seed beetle Acanthoscelides obtectus (Say)
Treść / Zawartość
Oviposition behaviour is recognized as an ecologically significant trait in insects. Since herbivorous insect females have a potential to lay eggs on unsuitable host species, it is hypothesized that this behaviour may be the first step in host-range expansion. The most intriguing phenomenon, found in some insect species, is the ability of females to lay eggs on unsuitable places if hosts are unavailable; this behaviour is termed ‘egg-dumping’. Egg-dumping can be adaptive plastic response in environments where hosts, either preferred or less suitable, may eventually become available. Transgenerational effects of this behaviour presume changes in larval feeding experience on different host species. Also, diverse larval experience may induce alterations in oviposition behaviour. To test whether egg laying behaviour of adult females can be modified by larval experience, we performed the experiment on two laboratory populations of Acanthoscelides obtectus (Say). First population (P) is housed in the laboratory on the common bean for 200 generations, whereas the second population (C) is derived from the first but has been raised for 197 generations on chickpea, a novel and less suitable host for larval development. In order to analyze differences between short-term and long-term effects of larval experience on eggdumping, both populations have been exposed to each host seed for one generation. The results of the study show that females from P population lay eggs more frequently in the absence of seeds when developed on chickpeas, compared with P females reared on beans. By contrast to P females, in C population, larval experience has no significant effects either on the number of dumped eggs or on the frequency of dumper females. These results demonstrate a significant inter-population diversification of phenotypic plasticity in egg-dumping behaviour depending on larval host experience. In other words, modification of oviposition behaviour, as a consequence of a long-term larval nutritional stress, can evoke previously unrecognized transgenerational effects.
- Bisby F.A., Buckingham J., Harborne J.B. 1994 – Phytochemical Dictionary of the Leguminosae – Chapman and Hall, London, 1180 pp.
- Cheng C-W., Yang R-L., Cheng I-C., Horng S-B. 2008 – Egg-dumping: a strategy for host range expansion in Callosobruchus maculatus (Coleoptera: Bruchidae) – Annals Ent. Soc. Am. 101: 950–954.
- Crispo E. 2007 – The Baldwin effect and genetic assimilation: revisiting two mechanisms of evolutionary change mediated by phenotypic plasticity – Evolution, 61: 2469–2479.
- Davis J.M. 2008 – Patterns of variation in the influence of natal experience on habitat choice – Quart. Rev. Biol. 83: 363–380.
- Ernande B., Dieckmann U. 2004 – The evolution of phenotypic plasticity in spatially structured environments: implications of intraspecific competition, plasticity costs and environmental characteristics – J. Evol. Biol. 17: 613–628.
- Futuyma D.J., Peterson S.C. 1985 – Genetic variation in the use of resource by insects – Ann. Rev. Entom. 30: 217–238.
- Huignard J., Biemont J.C. 1978 – Comparison of four populations of Acanthoscelides obtectus (Coleoptera Bruchidae) from different Colombian ecosystems: assay of interpretation – Oecologia, 35: 307–318.
- Lazarević J., Perić-Mataruga V., Stojković B., Tucić N. 2002 – Adaptation of the gypsy moth to an usuitable host plant – Ent. Exper. Applicata, 102: 75–86.
- Levins R. 1968 – Evolution in Changing Environments – Princeton University Press, Princeton, New Jersey, 132 pp.
- Messina F.J. 2004 – Predictable modification of body size and competitive ability following a host shift by a seed beetle – Evolution, 58: 2788–2797.
- Messina F.J., Fox, C.W. 2011 – Egg-dumping behavior is not correlated with wider host acceptance in the seed beetle Callosobruchus maculatus (Coleoptera: Chrysomelidae: Bruchinae) – Ann. Entomol. Soc. Am. 104: 850–856.
- Messina F.J., Fr y J.D. 2003 – Environmentdependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus – J. Evol. Biol. 16: 501–509.
- Messina F.J., Jones J.C. 2009 – Does rapid adaptation to a poor-quality host by Callosobruchus maculatus (F.) cause cross-adaptation to other legume hosts? – J. Stored Prod. Res. 45: 215–219.
- Messina F.J., Morrey J.L., Mendenhall M. 2007 – Why do host-deprived cowpea weevil ’dump’ their eggs? – Phys. Entom. 32: 259–267.
- Milanović D., Aleksić I., Tucić N. 1991– Nonrandom association between host acceptance and fitness – Zeitschrift fur Zoologische Systematik und Evolutionforschrung, 29: 108–114.
- Mousseau T.A., Fox C.W. 1998 – Maternal Effects as Adaptations – Oxford University Press, New York, 400 pp.
- Papaj D.R. 2000 – Ovarian dynamics and host use – Ann. Rev. Entom. 45: 423–448.
- Parsons D.M.H., Credland P.F. 2003 – Determination of oviposition in Acanthoscelides obtectus, a nonconformist bruchids – Phys. Entom. 28: 221–231.
- Pigliucci M. 2001 – Phenotypic Plasticity: Beyond Nature and Nurture – The Johns Hopkins University Press, Baltimore, Maryland, 344 pp.
- Price P.W. 1997 – Insect Ecology – John Wiley and Sons Inc., New York, 874 pp.
- SAS Institute 2003 – SAS/STAT user’s guide, v.9.1.3. – SAS Institute, Cary NC.
- Šešlija D., Stojković B., Tucić B., Tucić N. 2009 – Egg-dumping behaviour in the seed beetle Acanthoscelides obtectus selected for early and late reproduction – Eur. J. Entom. 106: 565–572.
- Sokal R.R., Rohlf F.J. 1994 – Biometry – W.H. Freeman, New York, 880 pp.
- Suzuki Y., Nijhout H.F. 2006 – Evolution of a polyphenism by genetic accommodation – Science, 311: 650–652.
- Tallamy D.W. 2005 – Egg dumping in insects – Ann. Rev. Entom. 50: 347–370.
- Thiery D., Jarry M., Pouzat J. 1994 – To penetrate or not to penetrate? A behavioral choice by bean beetle first-instar larvae in response to Phaseolus vulgaris seed surface quality – J. Chem. Ecol. 20: 1867–1875.
- Tucić N., Mikuljanac S., Stojković O. 1997 – Genetic variation and covariation among life history traits in populations of Acanthoscelides obtectus maintained on different hosts – Entom. Exper. Applicata, 85: 247–256.
- Tucić N., Milanović D., Mikuljanac S. 1995 – Laboratory evolution of host plant utilization in the bean weevil (Acanthoscelides obtectus) – Gen. Sel. Evol. 27: 491–502.
- Wang M.-H., Horng S.-B. 2004 – Egg dumping and life history strategy of Callosobruchus maculatus – Phys. Entom. 29: 26–31.
- Wehling W.F., Thompson J.N. 1997 – Evolutionary conservatism of oviposition preference in a widespread polyphagous insect herbivore, Papilio zelicaon – Oecologia, 111: 209–215.
- Wilson K., Hill L. 1989 – Factors affecting egg maturation in the bean weevil Callosobruchus maculatus – Phys. Entom. 14: 115–126.
- Yanagi S.-I., Tuda M. 2010 – Interaction effect among maternal environment, maternal investment and progeny genotype on life history traits in Callosobruchus chinensis – Funct. Ecol. 24: 383–391.