Photosynthetica, 2017 (vol. 55), issue 1

Photosynthetica 2017, 55(1):184-192 | DOI: 10.1007/s11099-016-0219-5

Photosynthetic responses of Chrysanthemum morifolium to growth irradiance: morphology, anatomy and chloroplast ultrastructure

S. Han1,2, S. M. Chen1, A. P. Song1, R. X. Liu1, H. Y. Li1, J. F. Jiang1, F. D. Chen1,*
1 College of Horticulture, Nanjing Agricultural University, Nanjing, China
2 College of Life Science, Shangqiu Normal University, Shangqiu, Henan, China

Seedlings of Chrysanthemum, cultivar 'Puma Sunny', were grown under a range of shading regimes (natural full sunlight, 55, 25, and 15% of full sunlight) for 18 days. Here, we characterized effects of varying light regimes on plant morphology, photosynthesis, chlorophyll fluorescence, anatomical traits, and chloroplast ultrastructure. We showed that leaf color was yellowish-green under full sunlight. Leaf area, internode length, and petiole length of plants were the largest under 15% irradiance. Net photosynthetic rate, water-use efficiency, PSII quantum efficiency, and starch grain were reduced with decreasing irradiance from 100 to 15%. Heavy shading resulted in the partial closure of PSII reaction centers and the CO2 assimilation was restricted. The results showed the leaves of plants were thinner under 25 and 15% irradiance with loose palisade tissue and irregularly arranged spongy mesophyll cells, while the plants grown under full sunlight showed the most compact leaf palisade parenchyma. Irradiance lesser than 25% of full sunlight reduced carbon assimilation and led to limited plant growth. Approximately 55% irradiance was suggested to be the optimal for Chrysanthemum morifolium.

Keywords: chlorophyll; dry mass; photochemical efficiency; photosystem; gas exchange

Received: November 1, 2015; Accepted: March 8, 2016; Published: March 1, 2017Show citation

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Han, S., Chen, S.M., Song, A.P., Liu, R.X., Li, H.Y., Jiang, J.F., & Chen, F.D. (2017). Photosynthetic responses of Chrysanthemum morifolium to growth irradiance: morphology, anatomy and chloroplast ultrastructure. Photosynthetica55(1), 184-192. doi: 10.1007/s11099-016-0219-5.
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References

  1. Ballare C.: Keeping up with the neighbours: phytochrome sensing and other signalling mechanisms. - Trends Plant Sci. 4: 97-102, 1999. Go to original source...
  2. Bilger W., Björkman O.: Role of the xanthophyll cycle in photoprotection elucidated by measurements of light-induced absorbance changes, fluorescence and photosynthesis in leaves of Hedera canariensis. - Photosynth. Res. 25: 173-185, 1990. Go to original source...
  3. Cavagnaro J., Trione S.: Physiological, morphological and biochemical responses to shade of Trichloris crinita, a forage grass from the arid zone of Argentina. - C J. Arid Environ. 68: 337-347, 2007. Go to original source...
  4. Correia M.J., Osório M.L., Osório J. et al.: Influence of transient shade periods on the effects of drought on photosynthesis, carbohydrate accumulation and lipid peroxidation in sunflower leaves. - Environ. Exp. Bot. 58: 75-84, 2006. Go to original source...
  5. Craven D.S., Gulamhussein S., Berlyn G.P.: Physiological and anatomical responses of Acacia koa (Gray) seedlings to varying light and drought conditions. - Environ. Exp. Bot. 69: 205-213, 2010. Go to original source...
  6. Dai Y.J., Shen Z.G., Liu Y. et al.: Effects of shade treatments on the photosynthetic capacity, chlorophyll fluorescence and chlorophyll content of Tetrastigma hemsleyanum Diels et Gilg. - Environ. Exp. Bot. 65: 177-182, 2009. Go to original source...
  7. Deng Y.M., Li C.C., Shao Q.S. 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, 2012.. Go to original source...
  8. Deng Y.M., Shao Q.S., Li C.C.: 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...
  9. Dimassi-Theriou K., Bosabalidis A.M.: Effects of light, magnesium and sucrose on leaf anatomy, photosynthesis, starch and total sugar accumulation, in kiwifruit cultured in vitro. - Plant Cell Tiss. Org. 47: 127-134, 1997. Go to original source...
  10. Evans J.R., Poorter H.: Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain. - Plant Cell Environ. 24: 755-767, 2001. Go to original source...
  11. Evans J.R.: Leaf anatomy enables more equal access to light and CO2 between chloroplast. - New Phytol. 143: 93-104, 1999. Go to original source...
  12. Favaretto V.F., Martinez C.A., Soriani H.H. et al.: Differential responses of antioxidant enzymes in pioneer and latesuccessional tropical tree species grown under sun and shade conditions. - C J. Exp. Bot. 70: 20-28, 2011. Go to original source...
  13. Fu W., Li P. Wu Y. et al.: Effects of different light intensities on chlorophyll fluorescence characteristics and yield in lettuce. - Sci. Hortic.-Amsterdam 135: 45-51, 2012.
  14. Garty J., Tamir O., Hassid I. et al: Photosynthesis, chlorophyll integrity, and spectral reflectance in lichens exposed to air pollution. - C J. Environ. Qual. 30: 884-893, 2001. Go to original source...
  15. Genty B., Briantais J.M., Braker N.R.: The relationship between quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescene. - Biochim. Biophys. Acta 990: 87-92, 1989. Go to original source...
  16. Genty B., Harbinson J.M., Baker N.R.: Relative quantum efficiencies of the two photosystems of and photorespiratory non-respiratory conditions. - Plant Physiol. Bioch. 28: 1-10, 1990.
  17. Goldschmidt E.E., Huber S.C.: Regulation of phosynthesis by end-product accumulation in leaves of plants storing starch, sucrose and hexose sugars. - Plant Physiol. 99: 1443-1448, 1992. Go to original source...
  18. Gregoriou K., Pontikis K., Vemmos S.: Effects of reduced irradiance on leaf morphology, photosynthetic capacity, and fruit yield in olive (Olea europaea L.). - Photosynthetica 45: 172-181, 2007. Go to original source...
  19. Guidi L., Tonini M., Soldatini G.F.: Effects of high light and ozone fumigation on photosynthesis in Phaseolus vulgaris. - Plant Physiol. Bioch. 38: 717-725, 2000. Go to original source...
  20. Han H., Gao S., Li B.F. et al.: Overexpression of violaxanthin de-epoxidase gene alleviates photoinhibition of PSII and PSI in tomato during high light and chilling stress. - C J. Plant Physiol. 167: 176-183, 2010. Go to original source...
  21. Han S., Chen L.S., Jiang H.X. et al.: Boron deficiency decreases growth and photosynthesis, and increases starch and hexoses in leaves of citrus seedlings. - C J. Plant Physiol. 165: 1331-1341, 2008. Go to original source...
  22. Chen X.Y., Li W., Lu Q.T.: The xanthophyll cycle and antioxidative defense system are enhanced in the wheat hybrid subjected to high light stress. - C J. Plant Physiol. 168: 1828-1836, 2011.
  23. Krall J.P., Edwards G.E.: Relationship between photosystem II activity and CO2 fixation in leaves. - Physiol. Plantarum 86: 180-187, 1992. Go to original source...
  24. Kubínová L.: Stomata and mesophyll characteristics of barley leaf as affected by light: stereological analysis. - C J. Exp. Bot. 42: 995-1001, 1991. Go to original source...
  25. Li H.W., Li B., Zheng Q. et al.: Variation in photosynthetic traits and antioxidant enzyme activities in wheat seedlings transferred from low to high light growth condition. - Acta Agr. Sin. 36: 449-456, 2010.
  26. Lichtenthaler H.K.: Chlorophylls and carotenoids: pigments of photosynthetic biomembranes. - Method. Enzymol. 148: 350-382, 1987. Go to original source...
  27. Maxwell K., Johnson G.N.: Chlorophyll fluorescence-a practical guide. - CJ. Exp. Bot. 51: 659-668, 2000. Go to original source...
  28. Müller P., Li X.P., Niyogi K.K.: Non-photochemical quenching. A response to excess light energy. - Plant Physiol. 125: 1558-1566, 2001. Go to original source...
  29. Naramoto M., Katahata S.I., Mukai Y. et al.: Photosynthetic acclimation and photoinhibition on exposure to high light in shade-developed leaves of Fagus crenata seedlings. - Flora 201: 120-126, 2006. Go to original source...
  30. Osmond C.B.: What is photoinhibition? Some insights from comparisons of shade and sun plants. - In: Baker N.R., Bowyer J.R. (ed.): Photoinhibition of Photosynthesis, from the Molecular Mechanisms to the Field. Pp.1-24. BIOS Sci. Press, Oxford 1994.
  31. Paiva é.A.S., dos Santos Isaias R.M., Vale F.H.A. et al.: The influence of light intensity on anatomical structure and pigment contents of Tradescantia pallida (Rose) Hunt. CV. purpurea Boom (Commelinaceae) Leaves. - Braz. Arch. Biol. Technol. 46: 617-624, 2003.
  32. Quero J.L., Villar R., Marañón T. et al.: Interactions of drought and shade effects on seedlings of four Quercus species: physiological and structural leaf responses. - New Phytol. 170: 819-834, 2006. Go to original source...
  33. Schiefthaler U., Russell A.W., Bolh¨¤r-Nordenkampf H.R. et al: Photoregulation and photodamage in Schefflera arboricola leaves adapted to different light environments. - Aust. J. Plant Physiol. 26: 485-494, 1999. Go to original source...
  34. Skillman J. Garcia B.M., Virgo A. et al.: Growth irradiance effects on photosynthesis and growth in two co-occurring shade-tolerant neotropical perennials of contrasting photosynthetic pathways. - Am. J. Bot. 92: 1811-1899, 2005.
  35. Sui X.L., Mao S.L., Wang L. H. et al.: Effects of low light intensity on gas exchange and chlorophyll fluorescence characteristics of capsicum seedlings. - Acta Hortic. Sin. 34: 615-622, 2007.
  36. Valladares F., Chico J.M. Aranda I.: The greater seedlings highlight tolerance of Quercus robur over Fagus sylvatica is linked to a greater physiological plasticity. - Trees 16: 395-403, 2002. Go to original source...
  37. Veres S., Tóth V.R., Láposi R. et al.: Carotenoid composition and photochemical activity of four sandy grassland species. - Photosynthetica 44: 255-261, 2006. Go to original source...
  38. Wherley B., Gardner D., Metzger J.: Tall fescue photomorphogenesis as influenced by changes in the spectral composition and light intensity. - Crop Sci. 45: 562-568, 2005. Go to original source...
  39. Zavala J.A., Ravetta D.A.: Allocation of photoassimilates to biomass, resin and carbohydrates in Grindelia chiloensis as affected by light intensity. - Field Crop. Res. 69: 143-149, 2001. Go to original source...