Skip to main content

Advertisement

Log in

Life-history variation in a native perennial grass (Tridens flavus): reproductive allocation, biomass partitioning, and allometry

  • Published:
Plant Ecology Aims and scope Submit manuscript

Abstract

Investment of limited resources into reproduction is a common feature of plants; coadapted life-history traits function as adaptations that have evolved to maximize fitness. There is currently little known about reproductive allocation (RA) of perennial grasses as a component of a partitioning strategy evolved to optimize sexual reproduction or about how RA may be related allometrically to vegetative size. This study examined variation in RA, biomass partitioning, and allometry in populations of a caespitose perennial grass (Tridens flavus) native to eastern North America. Plants reared from seeds of five populations in central New Jersey, USA, were planted in July 2015 into two undisturbed gardens 30 m apart that differed in availability of sunlight and soil moisture. After 3 years, data were collected on number of seeds (fecundity) and dry mass of seeds, panicles, culms, and leaves. RA (seed mass/vegetative mass) was significantly higher (13.1%) in the garden with higher light and lower soil moisture compared to the other garden in which RA was lower (9.1%) and varied significantly among populations. Fecundity was tightly correlated with vegetative mass in both gardens. A weak, but significant, trade-off between seed mass and number occurred in the garden with lower light and higher soil moisture. RA was positively correlated with relative fitness in both gardens. This research illustrates how population differentiation in reproductive allocation and partitioning may be revealed only in specific environments. Relatively high investment in seed production is important for recruitment and expansion of caespitose perennial grasses throughout successional habitats.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Aarssen LW, Taylor DR (1992) Fecundity allocation in herbaceous plants. Oikos 65:225–232

    Google Scholar 

  • Abrahamson WG, Gadgil M (1973) Growth form and reproductive effort in goldenrods (Solidago, Compositae). Am Nat 107:651–661

    Google Scholar 

  • Adams DE, Wallace LL (1985) Nutrient and biomass allocation in five grass species in an Oklahoma tallgrass prairie. Am Mid Nat 113:170–181

    Google Scholar 

  • Aguilera MO, Lauenroth WK (1995) Influence of gap disturbance and type of microsites on seedling establishment in Bouteloua gracilis. J Ecol 83:87–97

    Google Scholar 

  • Bazzaz FA (1997) Allocation of resources in plants: state of the science and critical questions. In: Bazzaz FA, Grace J (eds) Plant resource allocation. Academic Press, San Diego, pp 1–37

    Google Scholar 

  • Bazzaz FA, Ackerly DD (1992) Reproductive allocation and reproductive effort in plants. In: Fenner M (ed) The ecology of regeneration in plant communities. CAB International, Wallingford, pp 1–26

    Google Scholar 

  • Boggess N, Baker BS (1983) Edaphic requirements and characteristics of purpletop. Agron J 75:53–56

    Google Scholar 

  • Bonser SP, Aarssen LW (2009) Interpreting reproductive allometry: individual strategies of allocation explain size-dependent reproduction in plant populations. Persp Plant Ecol Evol Syst 11:31–40

    Google Scholar 

  • Braendle C, Heyland A, Flatt T (2011) Integrating mechanistic and evolutionary analysis of life history variation. In: Flatt T, Heyland A (eds) Mechanisms of life history evolution. Oxford University Press, New York, pp 3–10

    Google Scholar 

  • Briske DD, Derner JD (1998) Clonal biology of caespitose grasses. In: Cheplick GP (ed) Population biology of grasses. Cambridge University Press, Cambridge, pp 106–135

    Google Scholar 

  • Cheplick GP (1995a) Life-history trade-offs in Amphibromus scabrivalvis (Poaceae): allocation to clonal growth, storage, and cleistogamous reproduction. Amer J Bot 82:621–629

    Google Scholar 

  • Cheplick GP (1995b) Plasticity of seed number, mass, and allocation in clones of the perennial grass Amphibromus scabrivalvis. Int J Plant Sci 156:522–529

    Google Scholar 

  • Cheplick GP (2005) The allometry of reproductive allocation. In: Reekie EG, Bazzaz FA (eds) Reproductive allocation in plants. Elsevier Academic Press, Burlington, pp 97–128

    Google Scholar 

  • Cheplick GP (2015) Approaches to plant evolutionary ecology. Oxford University Press, New York

    Google Scholar 

  • Cheplick GP (ms) Fitness components in populations of a native perennial grass (Tridens flavus): a three-year common garden experiment. [Unpublished manuscript]

  • Collins B, Wein G, Philippi T (2001) Effects of disturbance intensity and frequency on early old-field succession. J Veget Sci 12:721–728

    Google Scholar 

  • de Jong T, Klinkhamer P (2005) Evolutionary ecology of plant reproductive strategies. Cambridge University Press, Cambridge

    Google Scholar 

  • Foote LE, Jackobs JA (1966) Occurrence and stand density of Tridens flavus (L.) Hitchc. as related to some soil factors. Agron J 58:412–414

    Google Scholar 

  • Gotelli NJ, Ellison AM (2004) A primer of ecological statistics. Sinauer Associates, Sunderland

    Google Scholar 

  • Gross KL, Berner T, Marschall E, Tomcko C (1983) Patterns of resource allocation among five herbaceous perennials. Bull Torrey Bot Club 110:345–352

    Google Scholar 

  • Guàrdia R, Raventós J, Caswell H (2000) Spatial growth and population dynamics of a perennial tussock grass (Achnatherum calamagrostis) in a badland area. J Ecol 88:950–963

    Google Scholar 

  • Hancock JF, Pritts MP (1987) Does reproductive effort vary across different life forms and seral environments? A review of the literature. Bull Torrey Bot Club 114:53–59

    Google Scholar 

  • Hara T, Kawano S, Nagai Y (1988) Optimal reproductive strategy of plants, with special reference to the modes of reproductive resource allocation. Plant Sp Biol 3:43–59

    Google Scholar 

  • Harper JL (1977) Population biology of plants. Academic Press, San Diego

    Google Scholar 

  • Harper JL, Ogden J (1970) The reproductive strategy of higher plants. I. The concept of strategy with special reference to Senecio vulgaris L. J Ecol 58:681–688

    Google Scholar 

  • Hartnett DC (1990) Size-dependent allocation to sexual and vegetative reproduction in four clonal composites. Oecologia 84:254–259

    CAS  PubMed  Google Scholar 

  • Herben T, Šerá B, Klimešová J (2015) Clonal growth and sexual reproduction: tradeoffs and environmental constraints. Oikos 124:469–476

    Google Scholar 

  • Honu YAK, Gibson DJ, Middleton BA (2006) Response of Tridens flavus (L.) A. S. Hitchc. to soil nutrients and disturbance in an early successional old field. J Torrey Bot Soc 133:421–428

    Google Scholar 

  • Hutchings MJ (1997) Resource allocation patterns in clonal herbs and their consequences for growth. In: Bazzaz FA, Grace J (eds) Plant resource allocation. Academic Press, San Diego, pp 161–189

    Google Scholar 

  • Jurik TW (1983) Reproductive effort and CO2 dynamics of wild strawberry populations. Ecology 64:1329–1342

    Google Scholar 

  • Karlsson PS, Méndez A (2005) The resource economy of plant reproduction. In: Reekie EG, Bazzaz FA (eds) Reproductive allocation in plants. Elsevier Academic Press, Burlington, pp 1–49

    Google Scholar 

  • Kawano S (1981) Trade-off relationships between some reproductive characteristics in plants with special reference to life history strategy. Bot Mag Tokyo 94:285–294

    Google Scholar 

  • Kawano S, Miyake S (1983) The productive and reproductive biology of flowering plants. X. Reproductive energy allocation and propagule output of five congeners of the genus Setaria (Gramineae). Oecologia 57:6–13

    PubMed  Google Scholar 

  • Kleyer M, Minden V (2015) Why functional ecology should consider all plant organs: an allocation-based perspective. Basic Appl Ecol 16:1–9

    Google Scholar 

  • Kőrner C (1994) Biomass fractionation in plants: a reconsideration of definitions based on plant functions. In: Roy J, Garnier E (eds) A whole plant perspective on carbon-nitrogen interactions. SPB Academic Press, The Hague, pp 173–185

    Google Scholar 

  • Li C, Li H, Yang Y (2019) Senescence in growth and reproductive allocation in a bunchgrass. Plant Biol 21:300–306

    CAS  PubMed  Google Scholar 

  • Lovett Doust J (1989) Plant reproductive strategies and resource allocation. Trends Ecol Evol 4:230–234

    CAS  PubMed  Google Scholar 

  • Marbà N, Duarte CM, Agusti S (2007) Allometric scaling of plant life history. Proc Nat Acad Sci USA 104:15777–15780

    PubMed  Google Scholar 

  • Martinková Z, Honĕk A (1992) Effect of plant size on the number of caryopses in barnyard grass, Echinochloa crus-galli (Poaceae). Preslia Praha 64:171–176

    Google Scholar 

  • Mason CM, Goolsby EW, Davis KE, Bullock DV, Donovan LA (2017) Importance of whole-plant biomass allocation and reproductive timing to habitat differentiation across the North American sunflowers. Ann Bot 119:1131–1142

    PubMed  PubMed Central  Google Scholar 

  • McCarthy MC, Enquist BJ (2007) Consistency between an allometric approach and optimal partitioning theory in global patterns of plant biomass allocation. Funct Ecol 21:713–720

    Google Scholar 

  • Morris WF (2009) Life history. In: Levin SA (ed) The Princeton guide to ecology. Princeton University Press, Princeton, pp 126–136

    Google Scholar 

  • Moser LE, Burson BL, Sollenberger LE (2004) Warm-season (C4) grass overview. In: Moser LE, Burson BL, Sollenberger LE (eds) Warm-season (C4) grasses. American Society of Agronomy, Crop Science Society of America, Soil Science Society of America, Madison, pp 1–14

    Google Scholar 

  • Niklas KJ (1994) Plant allometry. University of Chicago Press, Chicago

    Google Scholar 

  • Niklas KJ, Enquist BJ (2003) An allometric model for seed plant reproduction. Evol Ecol Res 5:79–88

    Google Scholar 

  • Olszewski MW, Folin GJ (2009) Germination responses of purpletop and big bluestem caryopses subjected to distilled water or potassium nitrate prechilling, sodium hypochlorite, and storage. Hort Sci 44:1407–1411

    Google Scholar 

  • Partridge L, Harvey PH (1988) The ecological context of life history evolution. Science 241:1449–1454

    CAS  PubMed  Google Scholar 

  • Paul-Victor C, Turnbull LA (2009) The effect of growth conditions on the seed size/number trade-off. PLoS ONE 4:e6917. https://doi.org/10.1371/journal.pone.0006917

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Pitelka LF, Stanton DS, Peckenham MO (1980) Effects of light and density on resource allocation in a forest herb, Aster acuminatus (Compositae). Am J Bot 67:942–948

    Google Scholar 

  • Poorter H, Sack L (2012) Pitfalls and possibilities in the analysis of biomass allocation patterns in plants. Front Plant Sci 3:1–10

    Google Scholar 

  • Pyke DA (1990) Comparative demography of co-occurring introduced and native tussock grasses: persistence and potential expansion. Oecologia 82:537–543

    PubMed  Google Scholar 

  • Quinn JA, Hodgkinson KC (1984) Plasticity and population differentiation in reproductive characters and resource allocation in Danthonia caespitosa (Gramineae). Bull Torrey Bot Club 111:19–27

    Google Scholar 

  • Reekie EG (1998) An explanation for size-dependent reproductive allocation in Plantago major. Can J Bot 76:43–50

    Google Scholar 

  • Reekie EG (1999) Resource allocation, trade-offs, and reproductive effort in plants. In: Vuorisalo TO, Mutikainen (eds) Life history evolution in plants. Kluwer Academic, Dordrecht, pp 173–193

    Google Scholar 

  • Reznick D (2017) Evolution of life histories. In: Losos JB (ed) The Princeton guide to evolution. Princeton University Press, Princeton, pp 270–277

    Google Scholar 

  • Roos FH, Quinn JA (1977) Phenology and reproductive allocation in Andropogon scoparius (Gramineae) populations in communities of different successional stages. Amer J Bot 64:535–540

    Google Scholar 

  • Roybal CM, Butterfield BJ (2019) Species-specific trait-environment relationships among populations of widespread grass species. Oecologia 189:1017–1026

    PubMed  Google Scholar 

  • Salguero-Gómez R, Violle C, Gimenez O, Childs D (2018) Delivering the promises of trait-based approaches to the needs of demographic approaches, and vice versa. Funct Ecol 32:1424–1435

    PubMed  PubMed Central  Google Scholar 

  • Samson DA, Werk KS (1986) Size-dependent effects in the analysis of reproductive effort in plants. Am Nat 127:667–680

    Google Scholar 

  • Sarath G, Baird LM, Mitchell RB (2014) Senescence, dormancy and tillering in perennial C4 grasses. Plant Sci 217:140–151

    PubMed  Google Scholar 

  • Schaffer WM, Gadgil MD (1975) Selection for optimal life histories in plants. In: Cody ML, Diamond JM (eds) Ecology and evolution of communities. Harvard University Press, Cambridge, pp 142–157

    Google Scholar 

  • Schmid B, Bazzaz FA, Weiner J (1995) Size dependency of sexual reproduction and of clonal growth in two perennial plants. Can J Bot 73:1831–1837

    Google Scholar 

  • Smith CC, Fretwell SD (1974) The optimal balance between size and number of offspring. Am Nat 108:499–506

    Google Scholar 

  • Stearns SC (1976) Life-history tactics: a review of the ideas. Quart Rev Biol 51:3–47

    CAS  PubMed  Google Scholar 

  • Stearns SC (1977) The evolution of life history traits: A critique of the theory and a review of the data. Ann Rev Ecol Syst 8:145–171

    Google Scholar 

  • Stearns SC (1989) Trade-offs in life-history evolution. Funct Ecol 3:259–268

    Google Scholar 

  • Stearns SC (1992) The evolution of life histories. Oxford University Press, New York

    Google Scholar 

  • Sugiyama S, Bazzaz FA (1998) Size dependence of reproductive allocation: the influence of resource availability, competition and genetic identity. Funct Ecol 12:280–288

    Google Scholar 

  • Thompson K, Stewart AJA (1981) The measurement and meaning of reproductive effort in plants. Am Nat 117:205–211

    Google Scholar 

  • United States Department of Agriculture (2002) Purpletop: Tridens flavus (L.) Hitchc. Plant Fact Sheet, Natural Resources Conservation Service, Plant Materials Program (https://plant-materials.nrcs.usda.gov)

  • Valdés-Reyna J (2003) Tridens Roem. & Schult. In: Barkworth ME, Capels KM, Long S, Piep MB (eds) Flora of North American North of Mexico, Volume 25, Magnoliophyta: Commelinidae (in part): Poaceae, part 2. Oxford University Press, New York, pp 33–40

    Google Scholar 

  • Venable DL (1992) Size-number trade-offs and the variation of seed size with plant resource status. Am Nat 140:287–304

    Google Scholar 

  • Weiner J (2004) Allocation, plasticity and allometry in plants. Pesp Plant Ecol Evol Syst 6:2017–2215

    Google Scholar 

  • Weiner J, Campbell LG, Pino J, Echarte L (2009) The allometry of reproduction within plant populations. J Ecol 97:1220–1233

    Google Scholar 

  • Welham CVJ, Setter RA (1998) Comparison of size-dependent reproductive effort in two dandelion (Taraxacum officinale) populations. Can J Bot 76:166–173

    Google Scholar 

  • Wenk EH, Falster DS (2015) Quantifying and understanding reproductive allocation schedules in plants. Ecol Evol 5:5521–5538

    PubMed  PubMed Central  Google Scholar 

  • Williams JL, Auge H, Maron JL (2008) Different gardens, different results: native and introduced populations exhibit contrasting phenotypes across common gardens. Oecologia 157:239–248

    PubMed  Google Scholar 

  • Wilson AM, Thompson K (1989) A comparative study of reproductive allocation in 40 British grasses. Funct Ecol 3:297–302

    Google Scholar 

  • Younginger BS, Sirová D, Cruzan MB, Ballhorn DJ (2017) Is biomass a reliable estimate of plant fitness? Appl Plant Sci 5:1600094

    Google Scholar 

Download references

Acknowledgements

The manuscript benefited greatly from the comments and suggestions of two anonymous reviewers.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to G. P. Cheplick.

Additional information

Communicated by Wayne Polley.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Cheplick, G.P. Life-history variation in a native perennial grass (Tridens flavus): reproductive allocation, biomass partitioning, and allometry. Plant Ecol 221, 103–115 (2020). https://doi.org/10.1007/s11258-019-00996-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11258-019-00996-z

Keywords

Navigation