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2010 | 32 | 3 |

Tytuł artykułu

Sun/shade adaptations of the photosynthetic apparatus of Hoya carnosa, an epiphytic CAM vine, in a subtropical rain forest in northeastern Taiwan

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Most past work on the ecophysiology of the Crassulacean acid metabolism (CAM) plant, Hoya carnosa, in the lab and in situ in Australia indicates that this epiphytic vine is better adapted to shaded, not exposed, locations, although a recent study of this species in Taiwan presents findings that run counter to this conclusion. Thus, photosynthetic characteristics of shaded and exposed individuals of H. carnosa were compared in situ in a subtropical rain forest in northeastern Taiwan in order to determine whether this CAM epiphyte is better adapted to the shade or the sun. Although leaves of shade plants had much greater chlorophyll concentrations than did those of sun plants, chlorophyll a/b ratios did not differ between the two groups of plants. Fluorescence measurements revealed some ability of leaves to acclimate to both shade and sun, although some evidence for photoinhibition (photoprotection) was observed in more exposed plants. Despite the latter, both exposed and shaded plants exhibited CAM, measured as diel fluctuations in leaf acidity, and CAM was more consistently found in the exposed plants. Furthermore, some evidence for more CAM at higher light availabilities was found. Overall, the results of this investigation reveal that H. carnosa in this subtropical rain forest in Taiwan exhibits adaptations to both high and low light levels, which should prove adaptive for an epiphytic vine with leaves on the same individual exposed to a wide range of exposure and shade in the host tree canopy.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

32

Numer

3

Opis fizyczny

p.575-581,fig.,ref.

Twórcy

autor
  • Taiwan Forestry Research Institute, 53 Nanhai Rd, Taipei 10066, Taiwan, ROC
  • Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, KS 66045, USA
autor
  • Taiwan Forestry Research Institute, 53 Nanhai Rd, Taipei 10066, Taiwan, ROC
autor
  • Taiwan Forestry Research Institute, 53 Nanhai Rd, Taipei 10066, Taiwan, ROC
  • Department of Life Science, National Taiwan Normal University, 88 Ting-Chou Road, Section 4, Taipei 116, Taiwan, ROC

Bibliografia

  • Adams WW III (1988) Photosynthetic acclimation and photoinhibition of terrestrial and epiphytic CAM tissues growing in full sunlight and deep shade. Aust J Plant Physiol 15:123–134
  • Adams WW III, Osmond CB, Sharkey TD (1987) Responses of two CAM species to different irradiances during growth and susceptibility to photoinhibition by high light. Plant Physiol 83:213–218
  • Adams WW III, Terashima I, Brugnoli E, Demmig B (1988) Comparisons of photosynthesis and photoinhibition in the CAM vine Hoya australis and several C3 vines growing on the coast of eastern Australia. Plant Cell Environ 11:173–181
  • Adams WW III, Volk M, Hoehn A, Demmig-Adams B (1992) Leaf orientation and the response of the xanthophyll cycle to incident light. Oecologia 90:404–410
  • Adams WW III, Demmig-Adams B, Barker DH, Kiley S (1996) Carotenoids and Photosystem II characteristics of upper and lower halves of leaves acclimated to high light. Aust J Plant Physiol 23:669–677
  • Björkman O (1981) Responses to different quantum flux densities. In: Lange OL, Nobel PS, Osmond CB, Ziegler H (eds) Physiological plant ecology. Responses to the physical environment, vol I. Springer, Berlin, pp 57–107
  • Boardman NK (1977) Comparative photosynthesis of sun and shade plants. Annu Rev Plant Physiol 28:355–377
  • Demmig-Adams B, Adams WW III, Barker DH, Logan BA, Bowling DR, Verhoeven AS (1996) Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation. Physiol Plant 98:253–264
  • Demmig-Adams B, Adams WW III, Mattoo A (Eds) (2006) Photoprotection, photoinhibition, gene regulation, and environment. Springer, Dordrecht, p 380
  • Griffiths H, Ong BL, Avadhani PN, Goh CJ (1989) Recycling of respiratory CO₂ during Crassulacean acid metabolism: alleviation of photoinhibition in Pyrrosia piloselloides. Planta 179:115–122
  • Hsu C-C, Lin T-C, Chiou W-L, Lin S-H, Lin K-C, Martin CE (2006) Canopy CO₂ concentrations and Crassulacean acid metabolism in Hoya carnosa in a subtropical rain forest in Taiwan: consideration of CO₂ availability and the evolution of CAM in epiphytes. Photosynthetica 44:130–135
  • Huang T-C (1998) Flora of Taiwan, 2nd edn, vol 4. Angiosperms–Dicotyledons (Diapensiaceae–Compositae). Editorial Committee of the Flora of Taiwan, Taipei, p 1217
  • Kluge M, Ting IP (1978) Crassulacean acid metabolism. Analysis of an ecological adaptation. Springer, Berlin, p 209
  • Knauft RL, Arditti J (1969) Partial identification of dark ¹⁴CO₂ fixation products in leaves of Cattleya (Orchidaceae). New Phytol 68:657–661
  • Lüttge U (1987) Carbon dioxide and water demand: Crassulacean acid metabolism (CAM), a versatile ecological adaptation exemplifying the need for integration in ecophysiological work. New Phytol 106:593–629
  • Martin CE, McLeod KW, Eades CA, Pitzer AF (1985) Morphological and physiological responses to irradiance in the CAM epiphyte Tillandsia usneoides L. (Bromeliaceae). Bot Gaz 146:489–494
  • Martin CE, Eades CA, Pitner RA (1986) Effects of irradiance on Crassulacean acid metabolism in the epiphyte Tillandsia usneoides L. (Bromeliaceae). Plant Physiol 80:26–32
  • Martin CE, McKee JM, Schmitt AK (1989) Responses of photosynthetic O₂ evolution to PPFD in the CAM epiphyte Tillandsia usneoides L. (Bromeliaceae). Photosyn Res 21:145–150
  • Martin CE, Tüffers A, Herppich WB, Von Willert DJ (1999) Utilization and dissipation of absorbed light energy in the epiphytic CAM bromeliad Tillandsia ionantha. Int J Plant Sci 160:307–313
  • Martin CE, Lin T-C, Hsu C-C, Lin S-H, Lin K-C, Hsia Y-J, Chiou WL (2004) Ecophysiology and plant size in a tropical epiphytic fern, Aplenium nidus, in Taiwan. Int J Plant Sci 165:65–72
  • Martin S, Davis R, Protti P, Lin T-C, Lin S-H, Martin CE (2005) The occurrence of Crassulacean acid metabolism in epiphytic ferns, with an emphasis on the Vittariaceae. Int J Plant Sci 166:623–630
  • Martin CE, Hsu R (C-C), Lin T-C (2009) The relationship between CAM and leaf succulence in two epiphytic vines, Hoya carnosa and Dischidia formosana (Asclepiadaceae), in a subtropical rainforest in northeastern Taiwan. Photosynthetica 47:445–450
  • Moran R (1982) Formulae for determination of chlorophyllous pigments extracted with N, N-dimethylformamide. Plant Physiol 69:1376–1381
  • Osmond CB (1978) Crassulacean acid metabolism: a curiosity in context. Annu Rev Plant Physiol 29:379–414
  • Skillman JB, Winter K (1997) High photosynthetic capacity in a shade-tolerant Crassulacean acid metabolism plant. Implications for sunfleck use, nonphotochemical energy dissipation, and susceptibility to photoinhibition. Plant Physiol 113:441–450
  • Sokal RR, Rohlf FJ (1981) Biometry. The principles and practice of statistics in biological research, 2nd edn. WH Freeman & Co, New York, p 859
  • Wanntorp L, Van Donkelaar R, Renner SS (2006) Towards a monophyletic Hoya (Marsdenieae, Apocynaceae): inferences from the chloroplast trnL region and the rbcL-atpB spacer. Syst Bot 31:586–596
  • Winter K, Osmond CB, Hubick KT (1986) Crassulacean acid metabolism in the shade. Studies on an epiphytic fern, Pyrrosia longifolia, and other rainforest species from Australia. Oecologia 68:224–230

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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