Skip to main content
Log in

Sex expression, female frequency, and reproductive output in a gynodioecious clonal herb, Glechoma longituba (Lamiaceae)

  • Published:
Plant Ecology Aims and scope Submit manuscript

Abstract

We investigated the sex morphs and frequency of females in 24 natural populations of the clonal, gynodioecious species Glechoma longituba. In addition to the presence of hermaphrodites and females, there were some individuals with intermediate sex expression that could not be categorized as either morph. The majority of populations contained a predominance of hermaphrodites, although female frequency varied from 0 to 100%. The sexual expression of individual ramets did not change over three consecutive years or when ramets were transplanted to different populations, but it did change over the course of a flowering season. Seeds from females weighed more than those from hermaphrodites. The seed set of hermaphrodites was relatively constant across populations; the seed set of females was higher than that of hermaphrodites in most populations, but lower in populations in which females occurred at a very high frequency because of pollen limitation. This led to a negative correlation being detected between the seed set of females and the frequency of females in a population. We postulated that the adjustment of sex expression within seasons could be an adaptive mechanism of reproductive assurance in this system.

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

Access this article

Subscribe and save

Springer+
from $39.99 /Month
  • Starting from 10 chapters or articles per month
  • Access and download chapters and articles from more than 300k books and 2,500 journals
  • Cancel anytime
View plans

Buy Now

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

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Ågren J, Willson MF (1991) Gender variation and sexual differences in reproductive characters and seed production in gynodioecious Geranium maculatum. Am J Bot 78:470–480

    Article  Google Scholar 

  • Ashman TL (1999) Determinants of sex allocation in a gynodioecious wild strawberry: implications for the evolution of dioecy and sexual dimorphism. J Evol Biol 12:648–661

    Article  Google Scholar 

  • Ashman TL, Baker I (1992) Variation in floral sex allocation with time of season and currency. Ecology 73:1237–1243

    Article  Google Scholar 

  • Ashman TL, Hitchens MS (2000) Dissecting the causes of variation in intra-florescence allocation in a sexually polymorphic species, Fragaria virginiana (Rosaceae). Am J Bot 87:197–204

    Article  PubMed  Google Scholar 

  • Ashman TL, Pacyna J, Diefenderfer C, Leftwich T (2001) Size-dependent sex allocation in a gynodioecious wild strawberry: the effects of sex morph and inflorescence architecture. Int J Plant Sci 162:327–334

    Article  Google Scholar 

  • Asikainen E, Mutikainen P (2003) Female frequency and relative fitness of females and hermaphrodites in gynodioecious Geranium sylvaticum (Geraniaceae). Am J Bot 90:224–232

    Article  Google Scholar 

  • Barrett SCH (1992) Gender variation and the evolution of dioecy in Wurmbea dioica (Liliaceae). J Evol Biol 5:423–444

    Article  Google Scholar 

  • Barrett SCH, Case AL, Peters GB (1999) Gender modification and resource allocation in subdioecious Wurmbea dioica (Colchicaceae). J Ecol 87:123–137

    Article  Google Scholar 

  • Charlesworth D (1981) A further study of the problem of the maintenance of females in gynodioecious species. Heredity 46:27–39

    Article  Google Scholar 

  • Charlesworth B, Charlesworth D (1978) A model for the evolution of dioecy and gynodioecy. Am Nat 112:975–997

    Article  Google Scholar 

  • Charlesworth D (1999) Theories on the evolution of dioecy. In: Geber MA, Dawson TE, Delph LF (eds) Gender and sexual dimorphism in flowering plants. Springer, Berlin, pp 33–60

    Google Scholar 

  • Couvet D, Atlan L, Belhassen CG, Gouyon P-H, Kjellberg F (1990) Co-evolution between two symbionts: the case of cytoplasmic male-sterility in higher plants. Oxf Surv Evol Biol 6:225–249

    Google Scholar 

  • Darwin C (1877) The different forms of plants of the same species. John Murray, London

    Google Scholar 

  • Del Castillo RF (1993) Consequences of male sterility in Phacelia dubia. Evol Tre Pl 7:15–21

    Google Scholar 

  • Delph LF, Touzet P, Bailey MF (2006) Merging theory and mechanism in studies of gynodioecy. Trends Ecol Evol 22:17–24

    Article  PubMed  Google Scholar 

  • Delph LF, Wolf DE (2005) Evolutionary consequences of gender plasticity in genetically dimorphic breeding systems. New Phytol 166:119–128

    Article  PubMed  Google Scholar 

  • Delph LF (1990) Sex ratio variation in the gynodioecious shrub Hebe strictissima (Scrophulariaceae). Evolution 44:134–142

    Article  Google Scholar 

  • Delph LF (2003) Sexual dimorphism in gender plasticity and its consequences for breeding system evolution. Evol Dev 5:1, 34–39

    Article  Google Scholar 

  • Delph LF, Carroll SB (2001) Factors affecting relative seed fitness and female frequency in a gynodioecious species, Silene acaulis. Evol Ecol Res 3:487–505

    Google Scholar 

  • Delph LF, Lloyd DG (1991) Environmental and genetic control of gender in the dimorphic shrub Hebe subalpina. Evolution 45:1957–1964

    Article  Google Scholar 

  • Dommee B, Assouad MW, Valdeyron G (1978) Natural selection and gynodioecy in Thymus vulgaris L. Bot J Linn Soc 77:17–28

    Article  Google Scholar 

  • Dulberger R, Horovtiz A (1984) Gender polymorphism in flowers of Silene vulgaris (Caryophyllaceae). Bot J Linn Soc 89:101–117

    Article  Google Scholar 

  • Ehlers BK, Thompson JD (2004) Temporal variation in sex allocation in hermaphrodites of gynodioecious Thymus vulgaris L. J Ecol 92:15–23

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Gouyon PH, Couvet D (1988) A conflict between two sexes, females and hermaphrodites. In: Stearns SC (ed) The evolution of sex and its consequences. Birkhauser Verlag, Basel, Switzerland, pp 245–261

    Google Scholar 

  • Hermanutz LA, Innes DJ (1994) Gender variation in Silene acaulis (Caryophyllaceae). Plant Syst Evol 191:69–81

    Article  Google Scholar 

  • Kesseli R, Jain SK (1984) An ecological genetic study of gynodioecy in Limnanthes douglasii (Limnanthaceae). Am J Bot 71:775–786

    Article  Google Scholar 

  • Koelewijn HP, van Damme JMM (1996) Gender variation, partial male sterility and labile sex expression in gynodioecious plantago coronopus. New phytol 132:67–76

    Article  Google Scholar 

  • Krohne DT, Baker T, Baker HG (1980) The maintenance of the gynodioecious breeding system in Plantago lanceolata L. Am Mid Nat 103:269–279

    Article  Google Scholar 

  • Lewis D (1941) Male sterility in natural populations of hermaphrodite plants. New Phytol 40:56–63

    Article  Google Scholar 

  • His-Wen L (1977) Flora of China, vol 17, pp 118–119. Science press, Beijing (in Chinese)

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

    Google Scholar 

  • Lloyd DG (1974) Theoretical sex ratios of dioecious and gynodioecious angiosperms. Heredity 32:11–34

    Article  Google Scholar 

  • Lloyd DG (1980) Sexual strategies in plants. I. An hypothesis of serial adjustment of maternal investment during one reproductive session. New Phytol 86:69–79

    Article  Google Scholar 

  • McCauley DE, Brock MT (1998) Frequency-dependent fitness in Silene vulgaris, a gynodioecious plant. Evolution 52:30–36

    Article  Google Scholar 

  • McCauley DE, Taylor DR (1997) Local population structure and sex ratio: evolution in gynodioecious plants. Am Nat 150:406–419

    Article  PubMed  CAS  Google Scholar 

  • Molina-Freaner F, Jain SK (1992) Female frequencies and fitness components between sex phenotypes among gynodioecious populations of the colonizing species Trifolium hirtum AII. In California. Oecologia 63:279–286

    Article  Google Scholar 

  • Ross MD (1970) Digenic inheritance of male-sterility in Plantago lanceolata. Can J Cytol 11:739–744

    Google Scholar 

  • Ross MD (1978) The evolution of gynodioecy and subdioecy. Evolution 32:174–188

    Article  Google Scholar 

  • Shykoff JA (1988) Maintenance of gynodioecy in Silene acaulis (Caryophyllaceae): stage-specific fecundity and viability selection. Am J Bot 75:844–850

    Article  Google Scholar 

  • Shykoff JA (1992) Sex polymorphism in Silene acaulis (Caryophyllaceae) and the possible role of sexual selection in maintaining females. Am J Bot 79:138–143

    Article  Google Scholar 

  • Slade AJ, Hutchings MJ (1989) Within- and between population variation in ramet behaviour in the gynodioecious clonal herb, Glechoma hederacea (Labiatae). Can J Bot 67:633–639

    Article  Google Scholar 

  • Widén B, Widén M (1990) Pollen limitation and distance-dependent fecundity in females of the clonal gynodioecious herb Glechoma hederacea (Lamiaceae). Oecologia 83:191–196

    Article  Google Scholar 

  • Widén M, Widén B (1999) Sex expression in the clonal gynodioecious herb Glechoma hederacea (Lamiaceae). Can J Bot 77:1689–1698

    Article  Google Scholar 

  • Wolfe LM, Shmida A (1995) Regulation of gender and flowering behavior in a sexually dimorphic desert shrub (Ochradenus baccatus) Delile (Resedaceae). Isr J Plant Sci 43:325–337

    Google Scholar 

  • Zhang YW (2007) Sex expression and the reproductive ecology in a gynodioecious- Glechoma longituba (Lamiaceae). PhD Dissertation, Wuhan University, Hubei, China

Download references

Acknowledgments

We like to thank Liao Kuo, Wang XueYi, Shi XiaoChuan, and Chen Lei for their assistance in the field. Lynda Delph assisted in manuscript preparation. This work was supported by a grant from Specialized Research Fund for the Doctoral Program of Higher Education.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ji-Min Zhao.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhang, YW., Wang, Y., Yu, Q. et al. Sex expression, female frequency, and reproductive output in a gynodioecious clonal herb, Glechoma longituba (Lamiaceae). Plant Ecol 199, 255–264 (2008). https://doi.org/10.1007/s11258-008-9430-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11258-008-9430-1

Keywords