Skip to main content
Log in

Intrapopulation gender variation in common ragweed (Asteraceae: Ambrosia artemisiifolia L.), a monoecious, annual herb

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

We measured variation in gender among individuals within populations of ragweed (Ambrosia artemisiifolia) in an abandoned old-field and in the greenhouse. There was great variability in sex expression, from all-female to approximately 78% male. Plants differed significantly in gender in different locations within the field. Plants in an area abandoned from agriculture one year previously were more male than plants in a nearby area abandoned four years previously. In the greenhouse, soil moisture treatments and levels of attack by spittlebugs (Philaenus spumarius) did not affect gender. Height was positively correlated with relative maleness in both populations. Plants with greater shoot weight were relatively more male in the greenhouse, but not in the field. The gender variation we observed either has a genetic basis or is controlled by environmental variables other than those we investigated.

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

  • Abul-Fatih HA, Bazzaz FA, Hunt R (1979) The biology of Ambrosia trifida. III. Growth and biomass allocation. New Phytol 83:829–838

    Google Scholar 

  • Allard HA (1945) Flowering behavior and natural distribution of the eastern ragweeds (Ambrosia) as affected by length of day. Ecology 26:387–394

    Google Scholar 

  • Austenson HM, Walton PD (1970) Relationships between initial seed weight and mature plant characteristics in spring wheat. Can J Plant Sci 50:53–58

    Google Scholar 

  • Barker PA, Freeman DC, Harper KT (1982) Variation in the breeding system of Acer grandidentatum. For Sci 28:563–572

    Google Scholar 

  • Bassett IJ, Crompton CW (1975) The biology of Canadian weeds. 11. Ambrosia artemisiifolia L. and A. psilostachya DC. Can J Plant Sci 55:463–476

    Google Scholar 

  • Bazzaz FA (1968) Succession on abandoned fields in the Shawnee Hills, southern Illinois. Ecology 49:924–936

    Google Scholar 

  • Bazzaz FA (1974) Ecophysiology of Ambrosia artemisiifolia: a successional dominant. Ecology 55:112–119

    Google Scholar 

  • Black JN (1959) Seed size in herbage legumes. Herb Abstr 29:235–241

    Google Scholar 

  • Charlesworth D, Charlesworth B (1981) Allocation of resources to male and female functions in hermaphrodites. Biol J Linn Soc 15:57–74

    Google Scholar 

  • Charnov EL (1982) The theory of sex allocation. Princeton University Press, Princeton NJ USA

    Google Scholar 

  • Freeman DC, Harper KT, Charnov EL (1980) Sex change in plants: old and new observations and new hypotheses. Oecologia (Berlin) 47:222–232

    Google Scholar 

  • Freeman DC, McArthur ED, Harper KT, Blauer AC (1981) Influence of environment on the floral sex ratio of monoecious plants. Evolution (Lawrence Kans) 35:194–197

    Google Scholar 

  • Garnock-Jones P (1986) Floret specialisation, seed production, and gender in Artemisia vulgaris (Asteraceae, Anthemideae). Bot J Linn Soc (in press)

  • Gebben AI (1965) The ecology of common ragweed, Ambrosia artemisiifolia L. in southwestern Michigan. PhD thesis, University Michigan, Ann Arbor MI USA

    Google Scholar 

  • Halkka O, Raatikainen M, Vasarainen A, Heinonen L (1967) Ecology and ecological genetics of Philaenus spumarius L. (Homoptera). Ann Zool Fenn 4:1–18

    Google Scholar 

  • Haskins FA, Gorz HJ (1975) Influence of seed size, planting depth, and companion crop on emergence and vigor of seedlings in sweetclover. Agron J 67:652–654

    Google Scholar 

  • Hendrix SD (1984a) Reactions of Heracleum lanatum to floral herbivory by Depressaria pastinacella. Ecology 65:191–197

    Google Scholar 

  • Hendrix SD (1984b) Variation in seed weight and its effects on germination in Pastinaca sativa L. (Umbelliferae). Am J Bot 71:795–802

    Google Scholar 

  • Hendrix SD, Trapp EJ (1981) Plant-herbivore interactions: insect induced changes in host plant sex expression and fecundity. Oecologia (Berlin) 49:119–122

    Google Scholar 

  • Jones KL (1936) Studies on Ambrosia. I. The inheritance of floral types in the ragweed, Ambrosia elatior. Am Midl Nat 17:673–699

    Google Scholar 

  • Keever C (1950) Causes of succession on old fields of the Piedmont, North Carolina. Ecol Monogr 20:231–250

    Google Scholar 

  • Lloyd DG (1980) Sexual strategies in plants. III. A quantitative method for describing the gender of plants. N Z J Bot 18:103–108

    Google Scholar 

  • Lloyd DG (1984) Gender allocations in outcrossing cosexual plants. In: Dirzo R, Sarukhan J (eds) Perspectives on plant population ecology. Sinauer Associates, Sunderland MA USA, pp 277–300

    Google Scholar 

  • Lloyd DG, Bawa KS (1984) Modification of the gender of seed plants in varying conditions. Evol Biol 17:255–338

    Google Scholar 

  • Lovett Doust J (1980) Floral sex ratios in andromonoecious Umbelliferae. New Phytol 85:265–273

    Google Scholar 

  • Lovett Doust J, Harper JL (1980) The resouce costs of gender and maternal support in an andromonoecious umbellifer, Smyrnium olusatrum L. New Phytol 85:251–264

    Google Scholar 

  • Payne WW (1963) The morphology of the inflorescence of ragweeds (Ambrosia-Franseria: Compositae). Am J Bot 50:872–880

    Google Scholar 

  • Pickett STA, Bazzaz FA (1978) Organization of an assemblage of early successional species on a soil moisture gradient. Ecology 59:1248–1255

    Google Scholar 

  • Primack RB, Lloyd DG (1980) Sexual strategies in plants. IV. The distributions of gender in two monomorphic shrub populations. N Z J Bot 18:109–114

    Google Scholar 

  • Putnam WL (1953) Notes on the bionomics of some Ontario cercopids (Homoptera). Can Entomol 85:244–248

    Google Scholar 

  • Raynal DJ, Bazzaz FA (1975) Interference of winter annuals with Ambrosia artemisiifolia in early successional fields. Ecology 56:35–49

    Google Scholar 

  • Ross MD, Gregorius H-R (1983) Outcrossing and sex function in hermaphrodites: a resource-allocation model. Am Nat 121:204–222

    Google Scholar 

  • Schaal BA (1980) Reproductive capacity and seed size in Lupinus texensis. Am J Bot 67:703–709

    Google Scholar 

  • Stanton ML (1984) Seed variation in wild radish: effect of seed size on components of seedling and adult fitness. Ecology 65:1105–1112

    Google Scholar 

  • Weaver CR, King DR (1954) The meadow spittlebug. Ohio Agric Exp Stn Res Bull 741:1–99

    Google Scholar 

  • Whitham TG, Mopper S (1985) Chronic herbivory: impacts on architecture and sex expression of pinyon pine. Science 228:1089–1091

    Google Scholar 

  • Willson MF, Ruppel KP (1984) Resource allocation and floral sex ratios in Zizania aquatica. Can J Bot 62:799–805

    Google Scholar 

  • Zimmerman JK, Weis IM (1983) Fruit size variation and its effects on germination and seedling growth in Xanthium strumarium. Can J Bot 61:2309–2315

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

McKone, M.J., Tonkyn, D.W. Intrapopulation gender variation in common ragweed (Asteraceae: Ambrosia artemisiifolia L.), a monoecious, annual herb. Oecologia 70, 63–67 (1986). https://doi.org/10.1007/BF00377111

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00377111

Key words

Navigation