Abstract
Here we investigate the long-cited pattern that throughout the eastern United States, Solidago species (goldenrods), and in particular S. canadensis displace Aster species and dominate old-field communities. Theory predicts that such a ubiquitous pattern of repeated dominance should be linked to competitive ability for a limiting resource. However, no one has investigated this possibility in old-fields, representing a potentially significant gap in our understanding of a common human-altered environment. We tested the hypothesis that S. canadensis is the superior competitor for light compared to other common co-occurring goldenrod species, and that the goldenrods in general are the superior competitors for light compared to coexisting aster species, which are typically less abundant. We tested this hypothesis by comparing the light attenuation abilities of four goldenrod species, S. canadensis, S. rugosa, S. gigantea, and Euthamia graminifolia, and three aster species, Aster novae-angliae, A. pilosus, and A. prenanthoides. Consistent with our hypothesis, S. canadensis had a greater ability to attenuate light than any of the other goldenrods at higher densities, and the goldenrods overall had a greater ability to attenuate light than the asters. By conducting a census in our study area, we verified that S. canadensis is locally the most abundant goldenrod and that goldenrods are more locally abundant than asters. Furthermore, by conducting a literature survey we found evidence that S. canadensis replaces A. pilosus through time. Thus we found a close correspondence between relative abundance in the field and light attenuation ability in field experiments. These results are consistent with theory predicting that competition for limiting resources, in this case light, explains patterns of dominance and relative abundance in old-field plant communities.
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References
Armesto JJ, Pickett STA (1985) Experiments on disturbance in old-field plant communities: impact on species richness and abundance. Ecology 66:230–240
Bakelaar RG, Odum EP (1978) Community and population level responses to fertilization in an old-field ecosystem. Ecology 59:660–665
Baskin JM, Baskin CC (1979) Germination strategy of oldfield aster (Aster pilosus). Am J Bot 66:1–5
Bazzaz FA (1968) Succession on abandoned fields in the Shawnee Hills, southern Illinois. Ecology 49:924–936
Bazzaz FA (1996) Plants in a changing environment. Cambridge University Press, Cambridge
Bowers MA (1993) Influence of herbivorous mammals on an old-field plant community: years 1–4 after disturbance. Oikos 67:129–141
Canham CD, Finzi AC, Pacala SW, Burbank DH (1994) Causes and consequences of resource heterogeneity in forests: interspecific variation in light transmission by canopy trees. Can J For Res 24:337–349
Cannell MGR, Grace J (1993) Competition for light: detection, measurement, and quantification. Can J For Res 23:1969–1979
Carson WP, Barrett GW (1988) Succession in old-field plant communities: effects of contrasting types of nutrient enrichment. Ecology 69:984–994
Carson WP, Peterson CJ (1990) The role of litter in an old-field community: impact of litter quantity in different seasons on plant species richness and abundance. Oecologia 85:8–13
Carson WP, Pickett STA (1990) Role of resources and disturbance in the organization of an old-field plant community. Ecology 71:226–238
Carson WP, Root RB (2000) Herbivory and plant species coexistence: community regulation by an outbreaking phytophagus insect. Ecol Monogr 70:73–99
Chmielewski JG, Semple JC (2001) The biology of Canadian weeds. 114. Symphyotrichum pilosum (Willd.) Nesom (Aster pilosus Willd.). Can J Plant Sci 81:851–865
Chmielewski JG, Semple JC (2003) The biology of Canadian weeds. 125. Symphyotrichum ericoides (L.) Nesom (Aster ericoides L.) and S. novae-angliae (L.) Nesom (A-novae-angliae L.). Can J Plant Sci 83:1017–1037
Durand LZ, Goldstein G (2001) Photosynthesis, photoinhibition, and nitrogen use efficiency in native and invasive tree ferns in Hawaii. Oecologia 126:345–354
Harpole WS, Tilman D (2006) Non-neutral patterns of species abundance in grassland communities. Ecol Lett 9:15–23
Hartnett DC, Bazzaz FA (1985) The integration of neighborhood effects by clonal genets in Solidago canadensis. J Ecol 73:415–427
Hubbell SP, Foster RB, O’Brien ST, Harms KE, Condit R, Wechsler B, Wright SJ, Loo de Lao S (1999) Light-gap disturbances, recruitment limitation, and tree diversity in a neotropical forest. Science 283:554–557
Huisman J (1999) Population dynamics of light-limited phytoplankton: microcosm experiments. Ecology 80:202–210
Keddy PA, Twolan SL, Wisheu IC (1994) Competitive effect and response rankings in 20 wetland plants: are they consistent across three environments? J Ecol 82:635–643
Keever C (1950) Mechanisms of plant succession on old fields of Lancaster County, Pennsylvania. Bull Torrey Bot Club 106:299–308
Leck MA, Leck CF (1998) A ten-year seed bank study of old field succession in central New Jersey. J Torrey Bot Soc 125:11–32
Mellinger MV, McNaughton SJ (1975) Structure and function of successional vascular plant communities in central New-York. Ecol Monogr 45:161–182
Miller TE, Burns JH, Munguia P, Walters EL, Kneitel JM, Richards PM, Mouquet N, Buckley HL (2005) A critical review of twenty years’ use of the resource-ratio theory. Am Nat 165:439–448
Pattison RR, Goldstein G, Ares A (1998) Growth, biomass allocation and photosynthesis of invasive and native Hawaiian rainforest species. Oecologia 117:449–459
R Development Core Team (2007) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna. http://www.R-project.org. Accessed on October 14, 2007
Rejmánek M (1989) Invasibility of plant communities. In: Mooney HA, DiCastri F, Groves RH, Kruger FJ, Rejmánek M, Williamson M (eds) Biological invasions: a global perspective. John Wiley & Sons, Chichester, UK, pp 369–377
SAS Institute, Inc (2003) JMP IN version 5.1. Cary
Schmid B, Bazzaz FA (1990) Plasticity in plant size and architechture in rhizome-derived Solidago and Aster. Ecology 71:523–535
Schmid B, Bazzaz FA (1992) Growth responses of rhizomatous plants to fertilizer application and interference. Oikos 65:13–24
Schmid B, Bazzaz FA (1994) Crown construction, leaf dynamics, and carbon gain in two perennials with contrasting architechture. Ecol Appl 64:177–203
Seabloom EW, Harpole WS, Reichman OJ, Tilman D (2003) Invasion, competitive dominance, and resource use by exotic and native California grassland species. Proc Natl Acad Sci USA 100:13384–13389
Sheppard AW, Shaw RH, Sforza R (2006) Top 20 environmental weeds for classical biological control in Europe: a review of opportunities, regulations and other barriers to adoption. Weed Res 46:93–117
Sokal RR, Rohlf FJ (1995) Biometry: the principles and practice of statistics in biological research. W.H. Freeman and Company, New York
Stevens MH (1999) Ph.D Dissertation
Stevens MHH, Bunker DE, Schnitzer SA, Carson WP (2004) Establishment limitation reduces species recruitment and species richness as soil resources rise. J Ecol 92:339–347
Tilman D (1982) Resource competition theory and community structure. Princeton University Press, NJ
Tilman D (1988) Dynamics and structure of plant communities. Princeton University Press, NJ
Tramer EJ (1975) The regulation of plant species diversity on an early successional old-field. Ecology 56:905–914
Vankat JL, Carson WP (1991) Floristics of a chronosequence corresponding to old field deciduous forest succession in southwestern Ohio. III. Post-disturbance vegetation. Bull Torrey Bot Club 118:385–391
Vankat JL, Snyder GW (1991) Floristics of a chronosequence corresponding to old field deciduous forest succession in southwestern Ohio. 1. Undisturbed vegetation. Bull Torrey Bot Club 118:365–376
Walck JL, Baskin JM, Baskin CC (2001) Why is Solidago shortii narrowly endemic and S. altissima geographically widespread? A comprehensive comparative study of biological traits. J Biogeogr 28:1221–1237
Werner PA, Bradbury IK, Gross RS (1980) The biology of Canadian weeds. 45. Solidago canadensis L. Can J Plant Sci 60:1393–1409
Wright SJ (2002) Plant diversity in tropical forests: a review of mechanisms of species coexistence. Oecologia 130:1–14
Zhang JJ, Stephenson DE, Semple JC, Oldham MJ (1999) COSEWIC status report on the crooked-stem aster Symphyotrichum prenanthoides. In: COSEWIC assessment and status report on the crooked-stem aster Symphyotrichum prenanthoides in Canada. Committee on the Status of Endangered Wildlife in Canada, pp 1–16
Acknowledgements
We would like to thank Calvin Ernst and Mark Feeley of Ernst Conservation Seed Company for allowing us to utilize their crop rows and for logistical help. We would also like to thank Linesville High School students (Linesville, PA) for their assistance with the experimental setup and data collection. We appreciate Daniel Bunker, Mark Jonas, Kelly O’Donnell, Massimo Pigliucci, and Christina Richards for their comments on earlier versions of this manuscript, and Norris Muth for providing his expertize on invasive species. Scott Meiners provided unpublished data from the Buell–Small Succession Study. This manuscript was significantly improved by comments from Karel Prach and two anonymous reviewers. This work was funded by NSF grant DEB-9903912 to Walter Carson and Martin H. H. Stevens, a University of Pittsburgh Honor’s College Brackenridge fellowship to Scott Stark, and logistical support from Miami University of Ohio to Joshua Banta.
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Banta, J.A., Stark, S.C., Stevens, M.H.H. et al. Light reduction predicts widespread patterns of dominance between asters and goldenrods. Plant Ecol 199, 65–76 (2008). https://doi.org/10.1007/s11258-008-9412-3
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DOI: https://doi.org/10.1007/s11258-008-9412-3