Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-26T16:48:27.116Z Has data issue: false hasContentIssue false

Natural history of Symmetrischema lavernella (Lepidoptera: Gelechiidae): a moth with two feeding strategies and the ability to induce fruit formation in the absence of pollination

Published online by Cambridge University Press:  06 January 2017

T’ai H. Roulston*
Affiliation:
Department of Environmental Sciences, University of Virginia, Charlottesville, Virginia, 22904-4123, United States of America Blandy Experimental Farm, Boyce, Virginia, 22620, United States of America
Stephanie Cruz-Maysonet
Affiliation:
Department of Environmental Sciences, University of Virginia, Charlottesville, Virginia, 22904-4123, United States of America Blandy Experimental Farm, Boyce, Virginia, 22620, United States of America
Amy L. Moorhouse
Affiliation:
Department of Biology, Minnesota State University Moorhead, Moorhead, Minnesota, 56563, United States of America
Sangmi Lee
Affiliation:
Hasbrouck Insect Collection, School of Life Sciences, Arizona State University, Tempe, Arizona, 85287-4501, United States of America
Amber N. Emerson
Affiliation:
Department of Biology, Howard University, Washington, District of Columbia, 20059, United States of America
*
4Corresponding author (e-mail: [email protected]).

Abstract

The moth Symmetrischema lavernella (Chambers) (Lepidoptera: Gelechiidae) has two feeding strategies on its host plant Physalis Linnaeus (Solanaceae): a fruitworm that feeds on developing ovules in a fruit and a budworm that consumes a floral bud. The fruitworm strategy occurs when a neonate caterpillar enters the ovary of a flower bud above a size threshold (~4 mm in Physalis heterophylla Nees), consumes the developing ovules, and pupates in the fruit. In P. heterophylla, occupancy of the ovary by S. lavernella causes fruit development to occur in the absence of pollination, indicating that the caterpillar initiates developmental pathways associated with pollination. The budworm strategy occurs in buds below ~4 mm, involves consumption of the ovary and immature anthers, and results in pupation inside the uninflated calyx. The two strategies co-occur on plants, determined by the sizes of the available buds at the time of oviposition. The most prominent natural enemy of S. lavernella using the fruitworm strategy was the frugivorous caterpillar Heliothis subflexa (Guenée) (Lepidoptera: Noctuidae), also a specialist of Physalis. The larger Heliothis subflexa feeds on the fruit externally, consumes S. lavernella, and caused 31.3% of fruitworm mortality in field surveys. Parasitoids included wasps (Hymenoptera) of the families Braconidae, Ichneumonidae, and Chalcididae.

Type
Behaviour & Ecology
Copyright
© Entomological Society of Canada 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

1

Present address: Department of Sociology and Anthropology, University of Puerto Rico, Río Piedras, San Juan, PR 00931, Puerto Rico

2

Present address: Department of Ecology, Evolution and Organismal Biology, Iowa State University, Ames, Iowa, 50011, United States of America

3

Present address: Houston Independent School District, Houston, Texas, 77092-8501, United States of America

Subject editor: Chris Schmidt

References

Bateman, M. 2006. Impact of plant suitability, biogeography, and ecological factors on associations between the specialist herbivore Heliothis subflexa G. (Lepidoptera: Noctuidae) and the species in its host genus, Physalis L. (Solanaceae), in west-central Mexico. Ph.D. thesis. North Carolina State University, Raleigh, North Carolina, United States of America. Available from https://repository.lib.ncsu.edu/handle/1840.16/4322 [accessed 18 November 2016].Google Scholar
Bates, D., Mächler, M., Bolker, B., and Walker, S. 2015. Fitting linear mixed-effects models using lme4. Journal of Statistical Software, 67: 148. https://doi.org/10.18637/jss.v067.i01.CrossRefGoogle Scholar
Bautista-Martinez, N., Lopez-Bautista, E., and Madriz, H.V. 2015. Percentage damage to tomatillo crops by Heliothis subflexa (Lepidoptera: Noctuidae) at various altitudes. Florida Entomologist, 98: 790791.CrossRefGoogle Scholar
Benda, N.D., Brownie, C., Schal, C., and Gould, F. 2009. Fruit abscission by Physalis species as defense against frugivory. Entomologia Experimentalis et Applicata, 130: 2127.CrossRefGoogle Scholar
Blanchard, A. and Knudson, E.C. 1982. A new species of Symmetrischema Povolný (Lepidoptera: Gelechiidae) from Texas. Proceedings of the Entomological Society of Washington, 84: 628631.Google Scholar
Brower, A.E. 1984. A list of the Lepidoptera of Maine Part 2, the microlepidoptera Section 2. Maine Agricultural Experiment Station Technical Bulletin, 114: 170.Google Scholar
Busck, A. 1903. A review of the American moths of the family Gelechiidae, with descriptions of new species. Proceedings of the United States National Museum, 25: 767938.CrossRefGoogle Scholar
Busck, A. 1931. Two new Peruvian microlepidoptera of economic importance (Gelechiidae and Oecophoridae). Proceedings of the Entomological Society of Washington, 33: 5963.Google Scholar
Chambers, V.T. 1874. Tineina from Texas. The Canadian Entomologist, 6: 229259.CrossRefGoogle Scholar
Des Vignes, W.G. 1979. Biology and description of stages of Symmetrischema capsica (Bradley & Povolný). Journal of the Agricultural Society of Trinidad and Tobago, 79: 116126.Google Scholar
Galil, J., Dulberger, R., and Rosen, D. 1970. The effects of Sycophaga sycomori L. on the structure and development of the synconia in Ficus sycomorus L. New Phytologist, 69: 103111. https://doi.org/10.1111/j.1469-8137.1970.tb04054.x.CrossRefGoogle Scholar
He, C. and Saedler, H. 2007. Hormonal control of the inflated calyx syndrome, a morphological novelty, in Physalis . The Plant Journal, 49: 935946. https://doi.org/10.1111/j.1365-313X.2006.03008.x.CrossRefGoogle ScholarPubMed
Hodges, R.W. 1998. The Gelechioidea. In Lepidoptera: moths and butterflies 1. Handbook of Zoology IV/35. Edited by N.P. Kristensen. Walter de Gruyter, Berlin, Germany. Pp. 131158.Google Scholar
Hu, J.-Y. and Saedler, H. 2007. Evolution of the inflated calyx syndrome in Solanaceae. Molecular Biology and Evolution, 24: 24432453. https://doi.org/10.1093/molbev/msm177.CrossRefGoogle ScholarPubMed
Karban, R. and Agrawal, A.A. 2002. Herbivore offense. Annual Review of Ecology and Systematics, 33: 641664. https://doi.org/10.1146/annurev.ecolsys.33.010802.150443.CrossRefGoogle Scholar
Karsholt, O., Mutanen, M., Lee, S., and Kaila, L. 2013. A molecular analysis of the Gelechiidae (Lepidoptera, Gelechioidea) with an interpretative grouping of its taxa. Systematic Entomology, 38: 334348. https://doi.org/10.1111/syen.12006.CrossRefGoogle Scholar
Keasar, T., Kalish, A., Becher, O., and Steinberg, S. 2005. Spatial and temporal dynamics of potato tuberworm (Lepidoptera: Gelechiidae) infestation in field-stored potatoes. Journal of Economic Entomology, 98: 222228. https://doi.org/http://dx.doi.org/10.1093/jee/98.1.222.CrossRefGoogle ScholarPubMed
Khan, M.R., Hu, J., and He, C. 2012. Plant hormones including ethylene are recruited in calyx inflation in Solanaceous plants. Journal of Plant Physiology, 169: 940948. https://doi.org/10.1016/j.jplph.2012.02.015.CrossRefGoogle ScholarPubMed
Lee, S., Hodges, R.W., and Brown, R.L. 2009. Checklist of Gelechiidae (Lepidoptera) in America north of Mexico. Zootaxa, 2231: 139.CrossRefGoogle Scholar
Petzold-Maxwell, J., Wong, S., and Arellano, C. 2011. Host plant direct defence against eggs of its specialist herbivore, Heliothis subflexa . Ecological Entomology, 36: 700708.CrossRefGoogle Scholar
Povolný, D. 1967. Genitalia of some Nearctic and Neotropic members of the tribe Gnorimoschemini (Lepidoptera, Gelechiidae). Acta Entomologica Musei Nationalis Pragae, 37: 51127.Google Scholar
Powell, J.A. and Povolný, D. 2001. Gnorimoschemini moths of coastal dune and scrub habitats in California (Lepidoptera: Gelechiidae). Holarctic Lepidoptera, 8(Supplement 1): 153.Google Scholar
R Development Core Team. 2013. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. Available from http://www.R-project.org [accessed 17 November 2016].Google Scholar
Roulston, T.H., Cane, J.H., and Buchmann, S.L. 2000. What governs the protein content of pollen: pollinator preferences, pollen-pistil interactions, or phylogeny? Ecological Monographs, 70: 617643.Google Scholar
Shaltiel-Harpaz, L., Gerling, D., and Graph, S. 2016. Control of the tomato leafminer, Tuta absoluta (Lepidoptera: Gelechiidae), in open-field tomatoes by indigenous natural enemies occurring in Israel. Journal of Economic Entomology, 109: 120131.CrossRefGoogle ScholarPubMed
Solomon, B.P. 1980. Frumenta nundinella (Lepidoptera, Gelechiidae) – life-history and induction of host parthenocarpy. Environmental Entomology, 9: 821825.CrossRefGoogle Scholar
Story, J.M., Boggs, K.W., Good, W.R., Harris, P., and Nowierski, R.M. 1991. Metzneria paucipunctella Zeller (Lepidoptera – Gelechiidae), a moth introduced against spotted knapweed – its feeding strategy and impact on two introduced Urophora spp (Diptera, Tephritidae). The Canadian Entomologist, 123: 10011007.CrossRefGoogle Scholar