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Responses of clonal growth and photosynthesis in Amomum villosum to different light environments

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Photosynthetica

Abstract

Clonal growth is of great importance for survival, growth, expansion, and resource utilization of some species. Knowing how clonal plants respond morphologically and physiologically to different light environments can be useful to explain their occurrence and abundance patterns under specific environmental conditions. Responses of clonal growth, leaf gas exchange, fluorescence emission, and photosynthetic pigment concentrations to different light environments (100, 60, 30, and 15%) were studied in Amomum villosum, grown in the traditional way for economic purpose in Xishuangbanna, southwest China. The results showed that A. villosum attained vigorous clonal growth under 30% and 60% light, with a higher plant height, number of ramets, stolon length, thicker stems and stolons. Shade-grown A. villosum possessed a larger leaf area than that of the sun-grown plants in order to capture more light. For A. villosum, the higher light-saturated net photosynthetic rate, light-saturation point, larger fresh and dry biomass can explained the better clonal growth for A. villosum under 30% and 60% light. Amomum villosum attained the highest values of minimal chlorophyll fluorescence under 100% light and the lowest values of maximum photochemical efficiency of PSII under 15% light. Our findings indicated that the full irradiance was too strong and 15% light was too weak for A. villosum plants. It was also verified by higher concentrations of photosynthetic pigments in the shaded plants compared to those grown under full sun light. Our results suggested that A. villosum seemed to be adapted to moderate light environment (60–30%) which was indicated by vigorous clonal growth and higher photosynthesis. This information is very useful to select clonal species for rainforest or understory projects. The cultivation of A. villosum in rainforest should not be done under too strong (100%) or too weak light environment (less than 15%).

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Abbreviations

Car:

carotenoid

Chl:

chlorophyll

FL:

full sunlight

F0 :

minimal fluorescence yield of the dark adapted state

Fv/Fm :

maximal quantum yield of PSII photochemistry

LCP:

light-compensation point

LSP:

light-saturation point

P Nmax :

lightsaturated net photosynthetic rate

R D :

dark respiration rate

S15:

15% shading

S30:

30% shading

S60:

60% shading

α:

apparent quantum yield

References

  • Aleric K.M., Kirkman L.K.: Growth and photosynthetic responses of the federally endangered shrub, Lindera melissifolia (Lauraceae), to varied light environments.–Am. J. Bot. 92: 682–689, 2005.

    Article  PubMed  Google Scholar 

  • Alpert P.: Effects of clonal integration on plant plasticity in Fragaria chiloensis.–Plant Ecol. 141: 99–106, 1999.

    Article  Google Scholar 

  • Arnon D.I.: Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris.–Plant Physiol. 24: 1–15, 1949.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bailey S., Horton P., Walters R.G.: Acclimation of Arabidopsis thaliana to the light environment: the relationship between photosynthetic function and chloroplast composition.–Planta 218: 793–802, 2004.

    Article  CAS  PubMed  Google Scholar 

  • Baker N.R.: Chlorophyll fluorescence: a probe of photosynthesis in vivo.–Annu. Rev. Plant Biol. 59: 89–113, 2008.

    Article  CAS  PubMed  Google Scholar 

  • Barth C., Krause G.H., Winter K.: Responses of photosystem I compared with photosystem II to high light stress in tropical shade and sun leaves.–Plant Cell Environ. 24: 163–176, 2001.

    Article  CAS  Google Scholar 

  • Bond B.J., Farnsworth B.T., Coulombe R.A., Winner W.E.: Foliage physiology and biochemistry in response to light gradients in conifers with varying shade tolerance.–Oecologia 120: 183–192, 1999.

    Article  Google Scholar 

  • Campos M.A.A., Uchida T.: Influence of shade on the growth of seedlings of three Amazon species.–Pesqui. Agropecu. Bras. 37: 281–288, 2002.

    Article  Google Scholar 

  • Catoni R., Granata M.U., Sartori F. et al.: Corylus avellana responsiveness to light variations: morphological, anatomical, and physiological leaf trait plasticity.–Photosynthetica 53: 35–46, 2015.

    Article  Google Scholar 

  • Chaves A.R., Ten-Caten A., Pinheiro H.A. et al.: Seasonal changes in photoprotective mechanisms of leaves from shaded and unshaded field-grown coffee (Coffea arabica L.) trees.–Trees 22: 351–361, 2008.

    Article  CAS  Google Scholar 

  • Chen H.Y., Klinka K.: Light availability and photosynthesis of Pseudotsuga menziesii seedlings grown in the open and in the forest understory.–Tree Physiol. 17: 23–29, 1997.

    Article  CAS  PubMed  Google Scholar 

  • DaMatta F.M.: Ecophysiological constraints on the production of shaded and unshaded coffee: a review.–Field Crop. Res. 86: 99–114, 2004.

    Article  Google Scholar 

  • Dong M.: Morphological responses to local light conditions in clonal herbs from contrasting habitats, and their modification due to physiological integration.–Oecologia 101: 282–288, 1995.

    Article  Google Scholar 

  • Dong M., Pierdominici M.G.: Morphology and growth of stolons and rhizomes in three clonal grasses, as affected by different light supply.–Vegetatio 116: 25–32, 1995.

    Google Scholar 

  • Feng Y.L., Cao K.F., Feng Z.L.: Thermal dissipation, leaf rolling and inactivation of PSII reaction centres in Amomum villosum.–J. Trop. Ecol. 18: 865–876, 2002a.

    Article  Google Scholar 

  • Feng Y.L., Li X.: The combined effects of soil moisture and irradiance on growth, biomass allocation, morphology and photosynthesis in Amomum villosum.–Agroforest. Syst. 71: 89–98, 2007.

    Article  Google Scholar 

  • Feng Z.L., Feng Y.L., Cao K.F.: Effects of light intensity on photoinhibition of photosynthesis and thermal dissipation in Amomum villosum Lour.–Acta Phytoecol. Sin. 26: 77–82, 2002b.

    CAS  Google Scholar 

  • Hanba Y.T., Kogami H., Terashima I.: The effect of growth irradiance on leaf anatomy and photosynthesis in Acer species differing in light demand.–Plant Cell Environ. 25: 1021–1030, 2002.

    Article  Google Scholar 

  • Huang D., Wu L., Chen J.R., Dong L.: Morphological plasticity, photosynthesis and chlorophyll fluorescence of Athyrium pachyphlebium at different shade levels.–Photosynthetica 49: 611–618, 2011.

    Article  CAS  Google Scholar 

  • Jackson R.B., Caldwell M.M.: Geostatistical patterns of soil heterogeneity around individual perennial plants.–J. Ecol. 81: 683–692, 1993.

    Article  Google Scholar 

  • Klimeš L., Klimešová J., Hendriks R., Groenendael J.: Clonal plant architecture: A comparative analysis of form and function.–In: Kroon H., Groenendael J. (ed.): The Ecology and Evolution of Clonal Plants. Pp.1–29. Backhuys Publishers, Leiden 1997.

    Google Scholar 

  • Koike T., Kitao M., Maruyama Y. et al.: Leaf morphology and photosynthetic adjustments among deciduous broad-leaved trees within the vertical canopy profile.–Tree Physiol. 21: 951–958, 2001.

    Article  CAS  PubMed  Google Scholar 

  • Laing W.A., Greer D.H., Schnell T.A.: Photoinhibition of photosynthesis causes a reduction in vegetative growth rates of dwarf bean (Phaseolus vulgaris) plants.–Funct. Plant Biol. 22: 511–520, 1995.

    CAS  Google Scholar 

  • Lam E., Oritz W., Mayfield S., Malkin R.: Isolation and characterization of a light-harvesting chlorophyll a/b protein complex associated with photosystem I.–Plant Physiol. 74: 650–655, 1984.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lechowicz M.J., Bell G.: The ecology and genetics of fitness in forest plants. II. Microspatial heterogeneity of the edaphic environment.–J. Ecol.79: 687–696, 1991.

    Article  Google Scholar 

  • Leverenz J.W.: Shades shoot structure of conifers and the photosynthetic response to light at two CO2 partial pressure.–Funct. Ecol. 9: 413–421, 1995.

    Article  Google Scholar 

  • Liscum E., Stowe Evans E.L.: Phototropism: A “simple” physiological response modulated by multiple interacting photosensory-response pathways.–Photochem. Photobiol. 72: 273–282, 2000.

    Article  CAS  PubMed  Google Scholar 

  • Liu H.M., Gao L., Zheng Z., Feng Z.L.: The impact of Amomum villosum cultivation on seasonal rainforest in Xishuangbanna, Southwest China.–Biodivers. Conserv. 15: 2971–2985, 2006.

    Article  Google Scholar 

  • Lusk C.H., Reich P.B., Montgomery R.A. et al.: Why are evergreen leaves so contrary about shade?–Trends Ecol. Evol. 23: 299–303, 2008.

    Article  PubMed  Google Scholar 

  • Matos F.S., Wolfgramm R., Gonçalves F.V. et al.: Phenotypic plasticity in response to light in the coffee tree.–Environ. Exp. Bot. 67: 421–427, 2009.

    Article  CAS  Google Scholar 

  • Oborny B., Bartha S.: Clonality in plant communities: an overview.–Abstracta Bot. 19: 115–127, 1995.

    Google Scholar 

  • Pires M.V., Almeida A.F., Figueiredo A.L. et al.: Photosynthetic characteristics of ornamental passion flowers grown under different light intensities.–Photosynthetica 49: 593–602, 2011.

    Article  CAS  Google Scholar 

  • Poorter L.: Growth responses of 15 rain-forest tree species to a light gradient: the relative importance of morphological and physiological traits.–Ecology 13: 396–410, 1999.

    Google Scholar 

  • Rohácek K.: Chlorophyll fluorescence parameters: the definitions, photosynthetic meaning, and mutual relationships.–Photosynthetica 40: 13–29, 2002.

    Article  Google Scholar 

  • Roiloa S.R., Retuerto R.: Responses of the clonal Fragaria vesca to microtopographic heterogeneity under different water and light conditions.–Environ. Exp. Bot. 61: 1–9, 2007.

    Article  Google Scholar 

  • Ryser P., Eek L.: Consequences of phenotypic plasticity vs. interspecific differences in leaf and root traits for acquisition of aboveground and belowground resources.–Am. J. Bot. 87: 402–411, 2000.

    Article  CAS  PubMed  Google Scholar 

  • Saitoh T., Seiwa K., Nishiwaki A.: Importance of physiological integration of dwarf bamboo to persistence in forest understorey: a field experiment.–J. Ecol. 90: 78–85, 2002.

    Article  Google Scholar 

  • Schneider S., Ziegler C., Melzer A.: Growth towards light as an adaptation to high light conditions in Chara branches–New Phytol. 172: 83–91, 2006.

    Article  PubMed  Google Scholar 

  • Thornley J.H.: Mathematical Models in Plant Physiology. Pp. 318. Academic Press, London 1976.

    Google Scholar 

  • Valladares F., Gianoli E., Gómez J.M.: Ecological limits to plant phenotypic plasticity.–New Phytol. 176: 749–763, 2007.

    Article  PubMed  Google Scholar 

  • Wilk J.A., Kramer A.T., Ashley M.V.: High variation in clonal vs. sexual reproduction in populations of the wild strawberry, Fragaria virginiana (Rosaceae).–Ann. Bot.-London 104: 1413–1419, 2009.

    Article  Google Scholar 

  • Wyka T., Robakowski P., Zytkowiak R.: Leaf age as a factor in anatomical and physiological acclimative responses of Taxus baccata L. needles to contrasting irradiance environments.–Photosynth. Res. 95: 87–99, 2008.

    Article  CAS  PubMed  Google Scholar 

  • Yang Z.J., Zheng H.S., Yin G.T. et al.: Influence of rubber plantation intercropping with Amomum villosum or coffee on soil fertility.–Forest Res. 8: 466–470, 1995.

    Google Scholar 

  • Yoshimura K.: Irradiance heterogeneity within crown affects photosynthetic capacity and nitrogen distribution of leaves in Cedrela sinensis.–Plant Cell Environ. 33: 750–758, 2010.

    CAS  PubMed  Google Scholar 

  • Zhang Q., Chen Y.J., Song L.Y. et al.: Utilization of lightflecks by seedlings of five dominant tree species of different subtropical forest successional stages under low-light growth conditions.–Tree. Physiol. 32: 545–553, 2012.

    Article  PubMed  Google Scholar 

  • Zhang S., Ma K., Chen L.Z.: Response of photosynthetic plasticity of Paeonia suffruticosa to changed light environments.–Environ. Exp. Bot. 49: 121–133, 2003.

    Article  Google Scholar 

  • Zhou S.Q.: Cultivation of Amomum villosum in tropical forests.–Forest. Ecol. Manage. 60: 157–162, 1993.

    Article  Google Scholar 

Download references

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Correspondence to X. J. Ma.

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Acknowledgments: This study was supported by Yuannan Base Construction for Seed and Seedling Breeding Required by National Essential Medicines of China (Treasury department 2013 NO.135), by creative group research project, Special Fund for Basic Scientific Research Business of Central Public Research Institutes (YZYN-13-01) of Institute of Medicinal Plant Development, by Chinese Academy of Medical Sciences: Germplasm Innovation and Breeding of Tropical Famous Medical Plants (121306), and by Special Support from Collaborative Innovation Research Center of South Medicines of Yunnan Provincial Education Department.

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Guo, Y.H., Yuan, C., Tang, L. et al. Responses of clonal growth and photosynthesis in Amomum villosum to different light environments. Photosynthetica 54, 396–404 (2016). https://doi.org/10.1007/s11099-016-0194-x

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  • DOI: https://doi.org/10.1007/s11099-016-0194-x

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