Field frequency and pattern of inheritance of the herbivory-defence trait “resistance-by-ducking” in the giant goldenrod (Solidago gigantea, Asteraceae)
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Keywords

candy-cane stems
ducking stems
goldenrod
inheritance pattern
resistance to herbivory
Solidago

How to Cite

Wise, M. (2018) “Field frequency and pattern of inheritance of the herbivory-defence trait ‘resistance-by-ducking’ in the giant goldenrod (Solidago gigantea, Asteraceae)”, Plant Ecology and Evolution, 151(2), pp. 271-277. doi: 10.5091/plecevo.2018.1408.

Abstract

Background and aims – For a more complete understanding of the eco-evolutionary dynamics of plant-herbivore interactions, it is important to know the genetic mechanisms that control defence traits, as well as the levels of genetic variation for these traits in plant populations. Here, I present results of a study of the occurrence and pattern of inheritance of the recently discovered trait of ‘resistance-by-ducking’ in the goldenrod Solidago gigantea (Asteraceae).
Methods – I grew maternal families of seedlings from fruits collected in a large field population of S. gigantea in southwestern Virginia, USA. I determined stem phenotype (ducking or erect) for 704 plants across 36 maternal families.
Key results – Of the 704 plants, 72% had ducking stems and 28% had erect stems. Employing bootstrapping with Hardy-Weinberg principles, I found that the pattern of inheritance was consistent with stem phenotype being controlled by a major gene, with the ducking morph being recessive to the erect morph. The allele frequencies for stem phenotype in the source population were estimated to be 0.85 ducking and 0.15 erect alleles.
Conclusions – These findings not only help inform ecological studies of ducking in S. gigantea, but they lay the groundwork for comparative studies of similar goldenrod species whose populations have differing proportions of ducking stems. For example, in all previous studies on populations of S. altissima, ducking stems have been the minority morph, occurring at a frequency of less than 20%. These results suggest that ducking may be costlier in S. altissima, while S. gigantea may face different ecological pressures, or has somehow overcome some of the costs of ducking.

https://doi.org/10.5091/plecevo.2018.1408
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References

Abrahamson W.G., Weis A.E. (1997) Evolutionary ecology across three trophic levels: goldenrods, gallmakers, and natural enemies. Princeton, NJ, Princeton University Press.

Abrahamson W.G., Ball Dobley K., Houseknecht H.R., Pecone C.A. (2005) Ecological divergence among five co-occurring species of old-field goldenrods. Plant Ecology 177: 43–56. https://doi.org/10.1007/s11258-005-2069-2

Denno R.F., McClure M.S. (1983) Variability: a key to understanding plant-herbivore interactions. In: Denno R.F., McClure M.S. (eds) Variable plants and herbivores in natural and managed systems: 1–12. New York, Academic Press.

Dorchin N., Clarkin C.E., Scott E.R., Luongo M.P., Abrahamson W.G. (2007) Taxonomy, life history, and population sex ratios of North American Dasineura (Diptera: Cecidomyiidae) on goldenrods (Asteraceae). Annals of the Entomological Society of America 100: 539–548. https://doi.org/10.1603/0013-8746(2007)100[539:TLHAPS]2.0.CO;2

Dorchin N., McEvoy M.V., Dowling T.A., Abrahamson W.G., Moore J.G. (2009) Revision of the goldenrod-galling Rhopalomyia species (Diptera: Cecidomyiidae) in North America. Zootaxa 2152: 1–35.

Dorchin N., Joy J.B., Hilke L.K., Wise M.J., Abrahamson W.G. (2015) Taxonomy and phylogeny of the Asphondylia species (Diptera: Cecidomyiidae) of North American goldenrods: challenging morphology, complex host associations, and cryptic speciation. Zoological Journal of the Linnaean Society 174: 256–304. https://doi.org/10.1111/zoj.12234

Gould F. (1983) Genetics of plant-herbivore systems: interactions between applied and basic study. In: Denno R.F., McClure M.S. (eds) Variable plants and herbivores in natural and managed systems: 599–653. New York, Academic Press.

Halverson K., Heard S.B., Nason J.D., Stireman III J.O. (2008) Origins, distribution, and local co-occurrence of polyploid cytotypes in Solidago altissima (Asteraceae). American Journal of Botany 95: 50–58. https://doi.org/10.3732/ajb.95.1.50

Hull-Sanders H.M., Johnson R.H., Owen H.A., Meyer G.A. (2009) Effects of polyploidy on secondary chemistry, physiology, and performance of native and invasive genotypes of Solidago gigantea (Asteraceae). American Journal of Botany 96: 762–770. https://doi.org/10.3732/ajb.1500995

Kennedy G.G., Barbour J.D. (1992) Resistance variation in natural and managed systems. In: Fritz R.S., Simms E.L. (eds) Plant resistance to herbivores and pathogens: 13–41. Chicago, The University of Chicago Press.

Kliebenstein D.J. (2014) Quantitative genetics and genomics of plant resistance to insects. Annual Plant Reviews 47: 235–262. https://doi.org/10.1002/9781119312994.apr0511

Maddox G.D., Root R.B. (1987) Resistance to 16 diverse species of herbivorous insects within a population of goldenrod, Solidago altissima: genetic variation and heritability. Oecologia 72: 8–14. https://doi.org/10.1007/BF00385037

Maddox G.D., Root R.B. (1990) Structure of the encounter between goldenrod (Solidago altissima) and its diverse insect fauna. Ecology 71: 2115–2124. https://doi.org/10.2307/1938625

Painter R.H. (1958) Resistance of plants to insects. Annual Review of Entomology 3: 267–290. https://doi.org/10.1146/annurev.en.03.010158.001411

Schlaepfer D.R., Edwards P.J., Semple J.C., Billeter R. (2008) Cytogeography of Solidago gigantea (Asteraceae) and its invasive ploidy level. Journal of Biogeography 35: 2119–2127. https://doi.org/10.1111/j.1365-2699.2008.01937.x

Semple J.C., Ringius G.S., Leeder C., Morton G. (1984) Chromosome numbers of goldenrods, Euthamia and Solidago (Compositae: Astereae). II. Additional counts with comments on cytogeography. Brittonia 36: 280–292. https://doi.org/10.2307/2806528

Semple J.C. (2016) An intuitive phylogeny and summary of chromosome number variation in the goldenrod genus Solidago (Asteraceae: Asterae). Phytoneuron 32: 1–9.

Strausbaugh P.D., Core E.L. (1978) Flora of West Virginia. 2nd Ed. Grantsville, West Virginia, Seneca Books, Inc.

Szymura M., Szymura T.H. (2016) Historical contingency and spatial processes rather than ecological niche differentiation explain the distribution of invasive goldenrods (Solidago and Euthamia). Plant Ecology 217: 565–582. https://doi.org/10.1007/s11258-016-0601-1

Uesugi A., Kessler A. (2016) Herbivore release drives parallel patterns of evolutionary divergence in invasive plant phenotypes. Journal of Ecology 104: 876–886. https://doi.org/10.1111/1365-2745.12542

van Dam N.M., Hare D.J., Elle E. (1999) Inheritance and distribution of trichome phenotypes in glandular and non-glandular Datura wrightii. Journal of Heredity 90: 220–227. https://doi.org/10.1093/jhered/90.1.220

Weber E. (2001) Current and potential ranges of three exotic goldenrods (Solidago) in Europe. Conservation Biology 15: 122–128. https://doi.org/10.1111/j.1523-1739.2001.99424.x

Wise M.J., Abrahamson W.G. (2008) Ducking as a means of resistance to herbivory in tall goldenrod, Solidago altissima. Ecology 89: 3275–3281. https://doi.org/10.1890/08-0277.1

Wise M.J. (2009) To duck or not to duck: resistance advantages and disadvantages of the candy-cane stem phenotype in tall goldenrod, Solidago altissima. New Phytologist 183: 900–907. https://doi.org/10.1111/j.1469-8137.2009.02879.x

Wise M.J., Yi C.G., Abrahamson W.G. (2009) Associational resistance, gall-fly preferences, and a stem dimorphism in Solidago altissima. Acta Oecologica 35: 471–476. https://doi.org/10.1016/j.actao.2008.12.005

Wise M.J., Abrahamson W.G., Cole J.A. (2010a) The role of nodding stems in the goldenrod-gall-fly interaction: a test of the “ducking” hypothesis. American Journal of Botany 97: 525–529. https://doi.org/10.3732/ajb.0900227

Wise M.J., Cole J.A., Carr D.E. (2010b) A field study of potential ecological costs of resistance by ‘stem ducking’ in tall goldenrod, Solidago altissima. Entomologia Experimentalis et Applicata 136: 271–280. https://doi.org/10.1111/j.1570-7458.2010.01022.x

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