Photosynthetica 2016, 54(3):381-389 | DOI: 10.1007/s11099-016-0199-5

Comparison of morphological and physiological characteristics in two phenotypes of a rare and endangered plant, Begonia fimbristipula Hance

Y. Wang1,5, L. Shao2,5, J. Wang1,5, H. Ren1,*, H. Liu3,4, Q. M. Zhang1, Q. F. Guo5, X. W. Chen2
1 Key Laboratory of Vegetation Restoration and Management of Degraded Ecosystems, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China
2 College of Life Science, Zhaoqing University, Zhaoqing, China
3 International Center for Tropical Botany, Department of Earth and Environment, Florida International University, Miami, Florida, USA
4 Forestry College, Guangxi University, Nanning, China
5 Eastern Forest Environmental Threat Assessment Center, USDA Forest Service, RTP, New York, USA

The rare and endangered plant, Begonia fimbristipula, shows red and green phenotypes, differentiated by a coloration of the abaxial leaf surface. In this study, we compared morphological and physiological traits of both phenotypes. The results showed that the red phenotype contained a significantly higher chlorophyll content, closer arrangement of chloroplasts, and a more developed grana. In addition, the red phenotype transferred significantly more light energy into the electron transport during the photoreaction. Similarly, the maximum photosynthetic rate, instantaneous water-use and light-use efficiencies of the red B. fimbristipula were all significantly higher than those of the green individuals. The differentiation between these two phenotypes could be caused by their different survival strategies under the same conditions; epigenetic variations may be in some correlation with this kind of phenotype plasticity. Red B. fimbristipula has an advantage in resource acquisition and utilization and possesses a better self-protection mechanism against changes in environmental conditions, therefore, it might adapt better to global climate change compared to the green phenotype. Further studies on the possible epigenetic regulation of those phenotypic differentiations are needed.

Keywords: anatomy; epigenetic; macronutrient; morphology; pigment

Received: August 17, 2015; Accepted: December 18, 2015; Published: September 1, 2016Show citation

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Wang, Y., Shao, L., Wang, J., Ren, H., Liu, H., Zhang, Q.M., Guo, Q.F., & Chen, X.W. (2016). Comparison of morphological and physiological characteristics in two phenotypes of a rare and endangered plant, Begonia fimbristipula Hance. Photosynthetica, 54(3), 381-389. doi: 10.1007/s11099-016-0199-5.
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    References

    1. Abraham E.M., Kyriazopoulos A.P., Parissi Z.M.: Growth, dry matter production, phenotypic plasticity, and nutritive value of three natural populations of Dactylis glomerata L. under various shading treatments.-Agroforest. Syst. 88: 287-299, 2014. Go to original source...
    2. Allen J.F., Forsberg J.: Molecular recognition in thylakoid structure and function.-Trends Plant Sci. 6: 317-326, 2001. Go to original source...
    3. Allis C.D., Jenuwein T., Reinberg D. et al. (ed.): Epigenetics. Pp. 408. Cold Spring Harbor Lab. Press, New York 2007.
    4. Boyko A., Kovalchuk I.: Epigenetic control of plant stress.-Environ. Mol. Mutagen. 49: 61-72, 2008. Go to original source...
    5. Bradshaw A.D.: Evolutionary significance of phenotypic plasticity in plants.-Adv. Genet. 13: 115-155, 1965. Go to original source...
    6. Chinnusamy V., Zhu J.K.: Epigenetic regulation of stress responses in plants.-Curr. Opin. Plant. Biol. 12: 133-139, 2009.
    7. Clausen J., Keck D., Hiesey W.M.: Experimental Studies on the Nature of Species. I. Effect of Varied Environments on Western North American Plants. Pp. 132. Carnegie Inst. Washington, Washington DC 1940.
    8. Coley P.D., Aide T.M.: Red coloration of tropical young leaves: a possible antifungal defence?-J. Trop. Ecol. 5: 293-300, 1989. Go to original source...
    9. Cooney L.J., Van Klink J.W., Hughes N.M. et al.: Red leaf margins indicate increased polygodial content and function as visual signals to reduce herbivory in Pseudowintera colorata.-New Phytol. 194: 488-497, 2012. Go to original source...
    10. Dalling J.W., Winter K., Nason J.D. et al.: The unusual life history of Alesis blackiana: a shade-persistent pioneer tree?-Ecology 82: 933-945, 2001. Go to original source...
    11. Davidson A.M., Jennions M., Nicotra A.B.: Do invasive species show higher phenotypic plasticity than native species and, if so, is it adaptive? A meta-analysis.-Ecol. Lett. 14: 419-431, 2011. Go to original source...
    12. Demmig-Adams B., Adams W.W.: Photoprotection in an ecological context: the remarkable complexity of thermal energy dissipation.-New Phytol. 172: 11-21, 2006. Go to original source...
    13. Deng Y., Li C., Shao Q. et al.: Differential responses of double petal and multi petal jasmine to shading: I. Photosynthetic characteristics and chloroplast ultrastructure.-Plant Physiol. Bioch. 55: 93-102, 2012a. Go to original source...
    14. Deng Y., Shao Q., Li C. et al.: Differential responses of double petal and multi petal jasmine to shading: II. Morphology, anatomy and physiology.-Sci. Hortic.-Amsterdam 144: 19-28, 2012b. Go to original source...
    15. Donato A.M., de Morretes B.L.: Plinia edulis-leaf architecture and scanning electron micrographs.-Braz. J. Pharmacogn. 23: 410-418, 2013. Go to original source...
    16. Dong M.: [Survey, Observation and Analysis of Terrestrial Biocommunities]. Pp. 38. Chinese Standard Press, Beijing 1996.[In Chinese]
    17. Gould K.S.: Nature's Swiss army knife: The diverse protective roles of anthocyanins in leaves.-J. Biomed. Biotechnol. 5: 314-320, 2004. Go to original source...
    18. Gu C.Z.: [Flora of China]. Pp. 194. Science Press, Beijing 1999.[In Chinese]
    19. Henderson I.R., Jacobsen S.E.: Epigenetic inheritance in plants.-Nature 447: 418-424, 2007. Go to original source...
    20. Holton T.A., Cornish E.C.: Genetics and biochemistry of anthocyanin biosynthesis.-Plant Cell 7: 1071-1083, 1995. Go to original source...
    21. Hughes N. M.: The photoprotective role of anthocyanin pigment in leaf tissues.-Photosynthetica 46: 637-640, 2009.
    22. Joesting H.M., McCarthy B.C., Brown K.J.: Determining the shade tolerance of American chestnut using morphological and physiological leaf parameters.-Forest. Ecol. Manage. 257: 280-286, 2009. Go to original source...
    23. Kim B.G., Kim J.H., Min S.Y. et al.: Anthocyanin content in rice is related to expression levels of anthocyanin biosynthetic genes.-J. Plant Biol. 50: 156-160, 2007. Go to original source...
    24. Kitajima M., Butler W.L.: Quenching of chlorophyll fluorescence and primary photochemistry in chloroplasts by dibromothymoquinone.-Biochim. Biophys. Acta 376: 105-115, 1975. Go to original source...
    25. Koerselman W., Meuleman A.F.M.: The vegetation N:P ratio: a new tool to detect the nature of nutrient limitation.-J. Appl. Ecol. 33: 1441-1450, 1996. Go to original source...
    26. Kordyum E., Klimenko E.: Chloroplast ultrastructure and chlorophyll performance in the leaves of heterophyllous Nuphar lutea (L.) Smith plants.-Aquat. Bot. 110: 84-91, 2013. Go to original source...
    27. Kubis S.E., Castilho A.M., Vershinin A.V. et al.: Retroelements, transposons and methylation status in the genome of oil palm (Elaeis guineensis) and the relationship to somaclonal variation.-Plant. Mol. Biol. 52: 69-79, 2003. Go to original source...
    28. Kurepin L.V., Farrow S., Walton L.J. et al.: Phenotypic plasticity of sun and shade ecotypes of Stellaria longipes in response to light quality signaling: Cytokinins.-Environ. Exp. Bot. 84: 25-32, 2012. Go to original source...
    29. Landhäusser S.M., Lieffers V.J.: Photosynthesis and carbon allocation of six boreal tree species grown in understory and open conditions.-Tree Physiol. 21: 243-250, 2001. Go to original source...
    30. Lee D.W.: Anthocyanins in leaves: distribution, phylogeny and development.-Adv. Bot. Res. 37: 37-53, 2002. Go to original source...
    31. Lee D.W., Collins T.M.: Phylogenetic and ontogenetic influences on the distribution of anthocyanins and betacyanins in leaves of tropical plants.-Int. J. Plant Sci. 162: 1141-1153, 2001. Go to original source...
    32. Lee D.W., Gould K.S.: Anthocyanins in leaves and other vegetative organs: An introduction.-Adv. Bot. Res. 37: 1-16, 2002. Go to original source...
    33. Li Q.Z., Li C.W., Yang T.W.: [Stress response and memory mediated by DNA methylation in plants.]-Plant Physiol. J. 50: 725-734, 2014.[In Chinese]
    34. Li H., Zhang G.C., Xie H.C., et al.: The effects of the phenol concentrations on photosynthetic parameters of Salix babylonica L.-Photosynthetica 53: 430-435, 2015. Go to original source...
    35. Lin Z.F., Li S.S., Lin G.Z., et al.: Superoxide dismutase activity and lipid peroxidation in relation to senescence of rice leaves.-Acta. Bot. Sin. 26: 605-615, 1984.
    36. Liu N., Guan L.: Linkages between woody plant proliferation dynamics and plant physiological traits in southwestern North America.-J. Plant. Ecol. 5: 407-416, 2012. Go to original source...
    37. Mattick J.S.: Non-coding RNAs: the architects of eukaryotic complexity.-EMBO Rep. 2: 986-991, 2001. Go to original source...
    38. Maxwell K., Johnson G.N.: Chlorophyll fluorescence-a practical guide.-J. Exp. Bot. 51: 659-668, 2000. Go to original source...
    39. Moreira N.S., Nascimento L.B.S., Leal-Casta M.V. et al.: Comparative anatomy of leaves of Kalanchoe pinnata and K. crenata in sun and shade conditions, as a support for their identification.-Braz. J. Pharmacogn. 22: 929-936, 2012. Go to original source...
    40. Moriuchi K.S., Winn A.A.: Relationships among growth, development and plastic response to environment quality in a perennial plant.-New Phytol. 166: 149-158, 2005. Go to original source...
    41. Murray J.R., Hackett W.P.: Dihydroflavonol reductase activity in relation to differential anthocyanin accumulation in juvenile and mature phase Hedera helix L.-Plant Physiol. 97: 343-351, 1991. Go to original source...
    42. Nicotra A.B. Atkin O.K., Bonser S.P. et al.: Plant phenotypic plasticity in a changing climate.-Trends Plant Sci. 15: 684-692, 2010. Go to original source...
    43. Nijs I., Ferris R., Blum H.: Stomatal regulation in a changing climate: a field study using free air temperature increase (FATI) and free air CO2 enrichment (FACE).-Plant Cell. Environ. 20: 1041-1050, 1997. Go to original source...
    44. Parkinson J.A., Allen S.E.: A wet oxidation procedure suitable for the determination of nitrogen and mineral nutrients in biological materials.-Commun. Soil Sci. Plant 6: 1-11. 1975.
    45. Pourcel L., Irani N.G., Koo A.J.K. et al.: A chemical complementation approach reveals genes and interactions of flavonoids with other pathways.-Plant J. 74: 383-397, 2013. Go to original source...
    46. Reddy V.S., Dash S., Reddy A.R.: Anthocyanin pathway in rice (Oryza sativa L.): identification of a mutant showing dominant inhibition of anthocyanins in leaf and accumulation of proanthocyanins in pericarp.-Theor. Appl. Genet. 91: 301-312, 1995. Go to original source...
    47. Schlichting C.D., Smith H.: Phenotypic plasticity: linking molecular mechanisms with evolutionary outcomes.-Evol. Ecol. 16: 189-211, 2002. Go to original source...
    48. Schulze E.D., Beck E., Müller-Hohenstein K.: Plant Ecology. Pp. 118. Springer-Verlag, Berlin 2002.
    49. Shao L., Liang K., Cheng X.W. et al.: [Effect of sucrose on growth of tissue culture seedling and anthocyanin accumulation in Begonia fimbristipula Hance on Dinghushan Mountain].-Chin. Agr. Sci. Bull. 28: 242-246, 2012.[In Chinese]
    50. Shao L., Liang K., Cheng X.W., et al.: [Natural growth characteristics of Begonia fimbristipula Hance population in different habitats of Dinghu Mountain].-Guangdong Agr. Sci. 40: 42-46, 2013.[In Chinese]
    51. Shao Q.S., Wang H.Z., Guo H.P. et al.: Effects of shade treatments on photosynthetic characteristics, chloroplast ultrastructure, and physiology of Anoectochilus roxburghii.-PLOS One. 9: e85996, 2014. Go to original source...
    52. Si C.C., Dai Z.C., Lin Y. et al.: Local adaptation and phenotypic plasticity both occurred in Wedelia trilobata invasion across a tropical island.-Biol. Invasions 16: 2323-2337, 2014. Go to original source...
    53. Škerget M., Kotnik P., Hadolin M. et al.: Phenols, proanthocyanidins, flavones and flavonols in some plant materials and their antioxidant activities.-Food. Chem. 89: 191-198, 2005. Go to original source...
    54. Souza R.P., Machado E.C., Silva J.A.B. et al.: Photosynthetic gas exchange, chlorophyll fluorescence and some associated metabolic changes in cowpea (Vigna unguiculata) during water stress and recovery.-Environ. Exp. Bot. 51: 45-56, 2004. Go to original source...
    55. Sultan S.E.: Phenotypic plasticity for plant development, function and life history.-Trends Plant Sci. 5: 537-542, 2000. Go to original source...
    56. Sun Y.Q., Yan F., Cui X.Y. et al.: Plasticity in stomatal size and density of potato leaves under different irrigation and phosphorus regimes.-J. Plant Physiol. 171: 1248-1255, 2014. Go to original source...
    57. Tessier J.T., Raynal D.J.: Use of nitrogen to phosphorus ratios in plant tissue as an indicator of nutrient limitation and nitrogen saturation.-J. Appl. Ecol. 40: 523-534, 2003. Go to original source...
    58. Titus J., Sullivan P.G.: Heterophylly in the yellow waterlily, Nuphar variegate (Nymphaeaceae): effects of [CO2], natural sediment type, and water depth.-Am. J. Bot. 88: 1469-1478, 2001. Go to original source...
    59. Wells C.L., Pigliucci M.: Adaptive phenotypic plasticity: the case of heterophylly in aquatic plants.-Perspect. Plant Ecol. 3: 1-18, 2000. Go to original source...
    60. Wolffe A.P., Matzke M.A.: Epigenetics: regulation through repression.-Science 286: 481-486, 1999. Go to original source...
    61. Xing F.W.: [Rare plants of China]. Pp. 129. Hunan Educ. Publ. House, Changsha 2005.[In Chinese]
    62. Xu X., Lu Z., Luo Y.F.: [Determination of trace elements in different graded leaves in Begonia fimbristipula Hance].-Guangdong. Trace. Elem. Sci. 4: 55-57, 2000.[In Chinese]
    63. Ye Z.P., Yu Q.: A coupled model of stomatal conductance and photosynthesis for winter wheat.-Photosynthetica 46: 637-640, 2008. Go to original source...
    64. Yuan Y.Y., Chiu L.W., Li L.: Transcriptional regulation of anthocyanin biosynthesis in red cabbage.-Planta 230: 1141-1153, 2009. Go to original source...
    65. Zhang L.Y., Li G.G.: [The factors affecting anthocyanin content in plantlets of Begonia fimbristipula in vitro II].-Acta. Bot. Yunnanica 8: 60-66, 1986.[In Chinese]
    66. Zhang L.Y., Li G.G., Guo J.Y.: [Some factors affecting the anthocyanin content in plantlets of Begonia fimbristipula in vitro I].-Acta Bot. Yunnanica 7: 195-202, 1985.[In Chinese]
    67. Zilberman D., Henikoff S.: Epigenetic inheritance in Arabidopsis: selective silence.-Curr. Opin. Genet. Dev. 15: 557-562, 2005 Go to original source...

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