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Natural selection on light response curve parameters in the herbaceous annual, Impatiens capensis

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Abstract

We tested for genetic variation in light response curves and their acclimation to sun versus shade in recombinant inbred lines (RILs) of the annual species Impatiens capensis derived from a cross between sun and shade populations. We exposed replicates of 49 RILs to experimentally manipulated light levels (open versus shade) in a greenhouse and measured photosynthetic light response curves, height, biomass, and reproduction. Plants were taller in the shade treatment, but we were unable to detect differences between light treatments (i.e., acclimation) in the maximal rate of photosynthesis, the light compensation point, or the quantum efficiency of photosynthesis. Genotypic selection analyses indicated that higher maximal rates of carbon assimilation and higher light compensation points (typical of sun-acclimated light curves) were favored by natural selection in both light treatments. Thus, it appears that the pattern of selection on photosynthetic parameters may not depend on light environment in this species.

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References

  • Argyres AZ, Schmitt J (1991) Microgeographic genetic structure of morphological and life history traits in a natural population of Impatiens capensis. Evolution 45:178–189

    Google Scholar 

  • Arnold SJ, Peterson CR (2002) A model for optimal reaction norms: the case of the pregnant garter snake and her temperature-sensitive embryos. Am Nat 160:306–316

    Article  Google Scholar 

  • Arntz AM, Delph LF (2001) Pattern and process: evidence for the evolution of photosynthetic traits in natural populations. Oecologia 127:455–467

    Article  Google Scholar 

  • Baskauf CJ, Eickmeier WG (1994) Comparative ecophysiology of a rare and a widespread species of Echinacea (Asteraceae). Am J Bot 81:958–964

    Google Scholar 

  • Bennington CC, McGraw JB (1995) Natural selection and ecotypic differentiation in Impatiens pallida. Ecol Monogr 65:303–323

    Google Scholar 

  • Buchmann N, Brooks JR, Rapp KD, Ehleringer JR (1996) Carbon isotope composition of C-4 grasses influenced by light and water supply. Plant Cell Environ 19:392–402

    CAS  Google Scholar 

  • Chazdon RL, Pearcy RW (1986) Photosynthetic responses to light variation in rainforest species. II. Carbon gain and photosynthetic efficiency during light flecks. Oecologia 69:524–531

    Google Scholar 

  • Chazdon RL (1992) Photosynthetic plasticity of two rain forest shrubs across natural gap transects. Oecologia 92:586–595

    Google Scholar 

  • Clough JM, Peet MM, Kramer PJ (1981) Effects of high atmospheric CO2 and sink size on rates of photosynthesis of a soybean cultivar. Plant Physiol 67:1007–1010

    CAS  Google Scholar 

  • Davies SJ (1998) Photosynthesis of nine pioneer Macaranga species from Borneo in relation to life history. Ecology 79:2292–2308

    Google Scholar 

  • Donohue K, Messiqua D, Hammond Pyle E, Heschel MS, Schmitt J (2000) Evidence of adaptive divergence in plasticity: density- and site-dependent selection on shade avoidance responses in Impatiens capensis. Evolution 54:1956–1968

    CAS  PubMed  Google Scholar 

  • Donohue K, Hammond Pyle E, Messiqua D, Heschel MS, Schmitt J (2001) Adaptive divergence in plasticity in natural populations of Impatiens capensis and its consequences for performance in novel habitats. Evolution 55:692–702

    CAS  PubMed  Google Scholar 

  • Dudley SA (1996) Differing selection on plant physiological traits in response to environmental water availability: a test of adaptive hypotheses. Evolution 50:92–102

    Google Scholar 

  • Dudley SA, Schmitt J (1996) Testing the adaptive plasticity hypothesis: density-dependent selection on manipulated stem length in Impatiens capensis. Am Nat 147:445–465

    Article  Google Scholar 

  • Ehleringer JR (1978) Implications of quantum yield differences on the distributions of 3 carbon and 4 carbon grasses. Oecologia 31:255–268

    Google Scholar 

  • Farquhar GD, Sharkey TD (1982) Stomatal conductance and photosynthesis. Annu Rev Plant Physiol 33:317–345

    Google Scholar 

  • Farris MA, Lechowicz MJ (1990) Functional interactions among traits that determine reproductive success in a native annual plant. Ecology 71:548–557

    Google Scholar 

  • Field CB (1988) On the role of photosynthetic responses in contrasting the habitat distribution of rainforest plants. Aust J Plant Physiol 15:343–358

    Google Scholar 

  • Garbutt K (1986) Genetic differentiation in leaf and whole plant photosynthetic capacity and unit leaf rate among clones of Phlox paniculata. Am J Bot 73:1364–1371

    Google Scholar 

  • Geber MA, Dawson TE (1990) Genetic variation in and co-variation between leaf gas exchange, morphology, and development in Polygonum arenastrum, an annual plant. Oecologia 85:153–158

    Google Scholar 

  • Geber MA, Dawson TE (1997) Genetic variation in stomatal and biochemical limitations to photosynthesis in the annual plant, Polygonum arenastrum. Oecologia 109:535–546

    Article  Google Scholar 

  • Givnish TJ (1988) Adaptation to sun and shade: a whole plant perspective. Aust J Plant Physiol 15:63–92

    Google Scholar 

  • Hacker SD, Bertness MD (1995) Morphological and physiological consequences of a positive plant interaction. Ecology 76:2165–2175

    Google Scholar 

  • Heschel MS, Hausmann NJ (2001) Population differentiation for abscisic acid sensitivity in response to drought in Impatiens capensis (Balsaminaceae). Int J Plant Sci 162:1253–1260

    Article  CAS  Google Scholar 

  • Heschel MS, Donohue K, Hausmann NJ, Schmitt J (2002) Population differentiation and natural selection for water-use efficiency in Impatiens capensis (Balsaminaceae). Int J Plant Sci 163:907–912

    Article  Google Scholar 

  • Hirose T, Werger MJA (1987) Maximizing daily canopy photosynthesis with respect to the leaf nitrogen allocation pattern in the canopy. Oecologia 72:520–526

    Google Scholar 

  • Kirkpatrick M, Lofsvold D, Bulmer M (1990) Analysis of the inheritance, selection, and evolution of growth trajectories. Genetics 124:979–993

    Google Scholar 

  • Kingsolver JG, Gomulkiewicz RS, Carter PA (2001) Variation, selection, and evolution of function-valued traits. Genetica 112–113:87–104

    Google Scholar 

  • Lambers H, Chapin FS III, Pons TL (1998) Plant physiological ecology. Springer, Berlin Heidelberg New York

  • Lande R, Arnold SJ (1983) The measurement of selection on correlated characters. Evolution 37:1210–1226

    Google Scholar 

  • Larcher W (1995) Physiological plant ecology, 3rd edn. Springer, Berlin Heidelberg New York

  • Littell RC, Milliken GA, Stroup WW, Wolfinger RD (1996) SAS System for Mixed Models. SAS Institute, Cary

  • Littell RC, Henry PR, Ammerman CB (1998) Statistical analysis of repeated measures data using SAS procedures. J Anim Sci 76:1216–1231

    CAS  PubMed  Google Scholar 

  • Marshall B, Biscoe PV (1980) A model for 3 carbon leaves describing the dependence of net photosynthesis on irradiance derivation. J Exp Bot 31:29–40

    CAS  Google Scholar 

  • Mooney HA (1991) Plant physiological ecology—determinants of progress. Funct Ecol 5:127–135

    Google Scholar 

  • Mooney HA, Field C, Gulmon SL, Bazzaz FA (1981) Photosynthesis capacity in relation to leaf position in desert vs. old field annuals. Oecologia 50:109–112

    Google Scholar 

  • Mulkey SS, Smith AP, Wright SJ (1991) Comparative life-history and physiology of 2 understory neotropical herbs. Oecologia 88:263–273

    Google Scholar 

  • Paoletti C, Holsinger KE (1999) Spatial patterns of polygenic variation in Impatiens capensis, a species with an environmentally controlled mixed mating system. J Evol Biol 12:689–696

    Article  Google Scholar 

  • Parkinson KJ (1985) A simple method for determining the boundary layer resistance in leaf cuvettes. Plant Cell Environ 8:223–226

    Google Scholar 

  • Pearcy RW, Sims DA (1994) Photosynthetic acclimation to changing light environments: scaling from the leaf to the whole plant. In: Caldwell MM, Pearcy RW (eds) Exploitation of environmental heterogeneity by plants: ecophysiological processes above- and belowground. Academic, San Diego, pp 145–174

  • Peek MS, Russek-Cohen E, Wait DA, Forseth IN (2002) Physiological response curve analysis using nonlinear mixed models. Oecologia 132:175–180

    Article  Google Scholar 

  • Potvin C, Lechowicz MJ, Tardif S (1990) The statistical analysis of ecophysiological response curves obtained from experiments involving repeated measures. Ecology 71:1389–1400

    Google Scholar 

  • Rausher MD (1992) The measurement of selection on quantitative traits: biases due to environmental covariances between traits and fitness. Evolution 46:616–626

    Google Scholar 

  • Scheiner SM, Gurevitch J, Teeri JA (1984) A genetic analysis of the photosynthetic properties of populations of Danthonia spicata that have different growth responses to light level. Oecologia 64:74–77

    Google Scholar 

  • Schemske DW (1984) Population structure and local selection in Impatiens pallida (Balsaminaceae), a selfing annual. Evolution 38:817–832

    Google Scholar 

  • Schmitt J (1993) Reaction norms of morphological and life-history traits to light availability in Impatiens capensis. Evolution 47:1654–1668

    Google Scholar 

  • Schoen DJ, Latta RG (1989) Spatial autocorrelation of genotypes in populations of Impatiens pallida and Impatiens capensis. Heredity 63:181–189

    Google Scholar 

  • Schoen DJ, Stewart SC Lechowicz MJ, Bell G (1986) Partitioning the transplant site effect in reciprocal transplant experiments with Impatiens capensis and Impatiens pallida. Oecologia 70:149–154

    Google Scholar 

  • Schulz KE, Smith M, Wu Y (1993) Gas exchange of Impatiens pallida Nutt. (Balsaminaceae) in relation to wilting under high light. Am J Bot 80:361–368

    Google Scholar 

  • Sims DA, Kelley S (1998) Somatic and genetic factors in sun and shade population differentiation if Plantago lanceolata and Anthoxanthum odoratum. New Phytol 140:75–84

    Article  Google Scholar 

  • Stinchcombe JR, Rausher MD (2001) Diffuse selection on resistance to deer herbivory in the Ivyleaf Morning glory, Ipomoea hederacea. Am Nat 158:376–388

    Article  Google Scholar 

  • Stinchcombe JR, Rutter MT, Burdick DS, Tiffin P, Rausher MD, Mauricio R (2002) Testing for environmentally induced bias in phenotypic estimates of natural selection: theory and practice. Am Nat 160:511–523

    Article  Google Scholar 

  • Sultan SE, Bazzaz FA (1993) Phenotypic plasticity in Polygonum persicaria. I. Diversity and uniformity in genotypic norms of reaction to light. Evolution 47:1009–1031

    Google Scholar 

  • Teramura AH, Strain BR (1979) Localized populational differences in the photosynthetic response to temperature and irradiance in Plantago lanceolata. Can J Bot 57:2559–2563

    Google Scholar 

  • Thornley JHM (1976) Mathematical models in plant physiology. Academic, New York

  • Valladares F, Wright SJ, Lasso E, Kitajima K, Pearcy RW (2000) Plastic phenotypic response to light of 16 congeneric shrubs from a Panamanian rainforest. Ecology 81:1925–1936

    Google Scholar 

  • Waller DM (1984) Differences in fitness between seedlings derived from cleistogamous and chasmogamous flowers in Impatiens capensis. Evolution 38:427–440

    Google Scholar 

  • Wulff RD (1989) The effects of reduced irradiance and low red to far red ratios on the growth and photosynthetic capacity in Impatiens capensis (Abstract 350). Am J Bot 76(Suppl):S131–S132

    Google Scholar 

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Acknowledgements

We thank A. Aguilera, B. Leib, and F. Jackson for help in maintaining our inbred lines and superb plant care. We are grateful to H. Urabe and M. Jackson for experimental assistance, and J. Kelley for discussions about non-linear curve fitting. Our research has been supported by NSF grant DEB 0129018.

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Correspondence to M. Shane Heschel.

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M. Shane Heschel and John R. Stinchcombe contributed equally to the paper.

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Heschel, M.S., Stinchcombe, J.R., Holsinger, K.E. et al. Natural selection on light response curve parameters in the herbaceous annual, Impatiens capensis . Oecologia 139, 487–494 (2004). https://doi.org/10.1007/s00442-004-1553-z

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