Skip to main content
Log in

GENDER DIMORPHISM AND ALTITUDINAL VARIATION OF SECONDARY COMPOUNDS IN LEAVES OF THE GYNODIOECIOUS SHRUB Daphne laureola

  • Published:
Journal of Chemical Ecology Aims and scope Submit manuscript

Abstract

In this article, we analyzed the concentration of coumarins in leaves of female and hermaphrodite individuals of the gynodioecious shrub Daphne laureola, along an elevational gradient in southern Spain. Combining HPLC and NMR techniques, we identified three different glycosides of 7-methoxy-coumarin in leaves of this species. Total coumarin concentration averaged between 60 and 120 mg/g dry weight for mature summer leaves of D. laureola growing at six different populations. As predicted by optimal theory, females tended to have a higher concentration of coumarins than hermaphrodites, thus upholding the idea that male reproductive function is costly for hermaphrodites. Furthermore, concentrations in females but not hermaphrodites were positively correlated with increasing population altitude, and the magnitude of gender divergence in coumarin concentration varied among populations, suggesting that the cost of the male function may be context dependent. To our knowledge, this is the first evidence of gender differences in chemical defenses of a gynodioecious species in the field.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ågren, J., Danell, K., Elmqvist, T., Ericson, L., and Hjältén, J. 1999. Sexual dimorphism and biotic interactions, pp. 217–246, M. A. Geber, T. E. Dawson, and L. F. Delph (eds.). Gender and Sexual Dimorphism in Flowering Plants. Springer, Berlin.

    Google Scholar 

  • Alonso, C. and Herrera, C. M. 1996. Variation in herbivory within and among plants of Daphne laureola (Thymelaeaceae): Correlation with plant size and architecture. J. Ecol. 84:495–502.

    Google Scholar 

  • Alonso, C. and Herrera, C. M. 2000. Seasonal variation in leaf characteristics and food selection by larval noctuids on an evergreen Mediterranean shrub. Acta Oecol. 21:257–265.

    Google Scholar 

  • Alonso, C. and Herrera, C. M. 2001. Neither vegetative nor reproductive advantages account for high frequency of male-steriles in southern Spanish gynodioecious Daphne laureola (Thymelaeaceae). Am. J. Bot. 88:1016–1024.

    Google Scholar 

  • Alonso, C. and Herrera, C. M. 2003. Developmental and spatial covariation of nutrients in growing leaves of Daphne laureola and their relationships with herbivory. New Phytol. 159:645–656.

    Google Scholar 

  • Ashman, T.-L. 2002. The role of herbivores in the evolution of separate sexes from hermaphroditism. Ecology 83:1175–1184.

    Google Scholar 

  • Berenbaum, M. R. 2001. Chemical mediation of coevolution: phylogenetic evidence for Apiaceae and associates. Ann. Mo. Bot. Gard. 88:45–59.

    Google Scholar 

  • Boecklen, W. J., Price, P. W., and Mopper, S. 1990. Sex and drugs and herbivores: sex-biased herbivory in arroyo willow (Salix lasiolepis). Ecology 71:581–588.

    Google Scholar 

  • Brown, S. A. 1970. Biosynthesis of furanocoumarins in parsnips. Phytochemistry 9:2471–2475.

    Google Scholar 

  • Cipollini, D., Purrington, C. B., and Bergelson, J. 2003. Costs of induced responses in plants. Basic Appl. Ecol. 4:79–85.

    Google Scholar 

  • Collin, C. L., Pennings, P. S., Rueffler, C., W idmer, S., and Shykoff, J. A. 2002. Natural enemies and sex: How seed predators and pathogens contribute to sex-differential reproductive success in a gynodioecious plant. Oecologia 131:94–102.

    Google Scholar 

  • Delph, L. F. 1990. Sex-differential resource allocation patterns in the subdioecious shrub Hebe subalpina. Ecology 71:1342–1351.

    Google Scholar 

  • Dudt, J. F. and Shure, D. J. 1994. The influence of light and nutrients on foliar phenolics and insect herbivory. Ecology 75:86–98.

    Google Scholar 

  • Eckhart, V. M. and Seger, J. 1999. Phenological and developmental costs of male sex function in hermaphroditic plants, pp. 195–213, T. O. Vuorisalo and P. K. Mutikainen (eds.). Life History Evolution in Plants. Kluwer, Dordrecht.

    Google Scholar 

  • Fung, S.-Y. and Herrebout, W. M. 1987. Coumarins in Prunus mahaleb and its herbivore the small ermine moth Yponomeuta mahalebellus. J. Chem. Ecol. 13:2041–2047.

    Google Scholar 

  • Gömez, D., Azorín, J., Bastida, J., Viladomat, F., and Codina, C. 2003. Seasonal and spatial variations of alkaloids in Merendera montanain relation to chemical defense and phenology. J. Chem. Ecol. 29:1117–1126.

    Google Scholar 

  • Gouyon, P. H. and Vernet, P. 1980. Étude la de variabilitégénétique dans une population de Thymus vulgaris L. Observations sur le polymorphismes sexuel et chimique, effets du régime de reproduction. Acta Oecol., Oecol. Plant. 1:165–178.

    Google Scholar 

  • Hegnauer, R. 1973. Chemotaxonomie der Pflanzen. VI. Thymeleaeceae. Birkauser Verlag, Basel.

    Google Scholar 

  • Herms, D. A. and Mattson, W. J. 1992. The dilemma of plants to grow or to defend. Quart. Rev. Biol. 67:283–334.

    Google Scholar 

  • Hoy, C. W., Head, G. P., and Hall, F. R. 1998. Spatial heterogeneity and insect adaptation to toxins. Annu. Rev. Entomol. 43:571–594.

    Google Scholar 

  • Jing, S. W. and Coley, P. D. 1990. Dioecy and herbivory: The effect of growth rate on plant defense in Acer negundo. Oikos 58:369–377.

    Google Scholar 

  • Johnson, K. and Scriber, J. M. 1994. Geographic variation in plant allelochemicals of significance to insect herbivores, pp. 7–31, T. N. Ananthakrishnan (ed.). Functional Dynamics of Phytophagous Insects. Science Publishers, Lebanon, New Hampshire, USA.

    Google Scholar 

  • Jung, M., Zinsmeister, H. D., and Geiger, H. 1994. New three- and tetraoxygenated coumarin glucosides from the mosses Atrichum undulatumand Polytrichum formosum. Z. Naturforsch 49c:697–702.

    Google Scholar 

  • Konishi, T., Wada, S., and Kiyosawa, S. 1993. Constituents of the leaves of Daphne pseudo-mezereum. Yakugaku Zasshi J. Pharm. Soc. Jap. 113:670–675.

    Google Scholar 

  • Louda, S. M. and Rodman, J. E. 1983. Ecological patterns in the glucosinolate content of a native mustard, Cardamine cordifolia, in the Rocky Mountains. J. Chem. Ecol. 9:397–422.

    Google Scholar 

  • Marshall, M. and Ganders, F. R. 2001. Sex-biased seed predation and the maintenance of females in a gynodioecious plant. Am. J. Bot. 88:1437–1443.

    Google Scholar 

  • Maynard-Smith, J. 1978. Optimization theory in evolution. Annu. Rev. Entomol. 9:31–56.

    Google Scholar 

  • Murray, R. D. H., Méndez, J., and Brown, S. A. 1982. The Natural Coumarins. Occurrence, Chemistry and Biochemistry. Wiley, Chichester, UK.

    Google Scholar 

  • Obeso, J. R. 2002. Tansley review no. 139. The costs of reproduction in plants. New Phytol. 155:321–348.

    Google Scholar 

  • Rozema, J., Chardonnens, A., Tosserams, M., H afkenscheid, R. and Bruijnzeel, S. 1997. Leaf thickness and UV-B absorbing pigments of plants in relation to an elevational gradient along the Blue Mountains, Jamaica. Plant Ecology 128:151–159.

    Google Scholar 

  • Salmore, A. K. and Hunter, M. D. 2001. Elevational trends in defense chemistry, vegetation, and reproduction in Sanguinaria canadensis. J. Chem. Ecol. 27:1713–1727.

    Google Scholar 

  • SAS Institute. 1996. SAS/STAT Software: Changes and Enhancements Through Release 6.11. SAS Institute, Cary, North Carolina.

  • Stratmann, J. 2003. Ultraviolet-B radiation co-opts defense signalling pathways. Trends. Plant. Sci. 8:526–533.

    Google Scholar 

  • Thompson, H. J. and Brown, S. A. 1984. Separations of some coumarins of higher plants by liquid chromatography. J. Chrom. 314:323–336.

    Google Scholar 

  • Ulubelen, A., Terem, B., and Tuzlaci, E. 1986. Coumarins and flavonoids from Daphne gnidioides. J. Nat. Prod. 49:692–694.

    Google Scholar 

  • Uno, G. E. 1982. Comparative reproductive biology of hermaphroditic and male-sterile Iris douglasiana Herb. (Iridaceae). Am. J. Bot. 69:818–823.

    Google Scholar 

  • Zobel, A. M. and Brown, S. A. 1988. Localization of daphnetin and umbelliferone in different tissues of Daphne mezereum shoots. Can. J. Bot. 67:1456–1459.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to CONCHITA ALONSO.

Rights and permissions

Reprints and permissions

About this article

Cite this article

ALONSO, C., PÉREZ, R., NIETO, P.M. et al. GENDER DIMORPHISM AND ALTITUDINAL VARIATION OF SECONDARY COMPOUNDS IN LEAVES OF THE GYNODIOECIOUS SHRUB Daphne laureola. J Chem Ecol 31, 139–150 (2005). https://doi.org/10.1007/s10886-005-0980-6

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10886-005-0980-6

Navigation