Effect of light intensities on the photosynthetic characteristics of Abies holophylla seedlings from different provenances
DOI:
https://doi.org/10.15287/afr.2014.266Keywords:
Abies holophylla seedling, provenance, light intensity, genetic difference, photosynthetic characteristicsAbstract
The photosynthetic characteristics of Abies holophylla seedlings from six provenances under four artificial light intensities in a greenhouse (full light, 75.08%, 55.42%, and 30.38% of full light) were studied to explore the underlying genetic differences in foliar photosynthesis. Varying light intensities significantly affected the foliar photosynthetic parameters of A. holophylla seedlings from six provenances. As the light intensity dropped, the foliar CO2 assimilation capacity of A. holophylla seedlings sharply decreased, and the foliar light utilization capacity significantly increased. Analysis of genetic variation showed highly significant differences in terms of CO2 assimilation capacity, light utilization capacity, and respiration depletion of A. holophylla seedlings among different provenances under different light intensities. The variations were mainly controlled by the genetic factors of the provenance itself. The obtained results revealed that different sensitivities of A. holophylla seedlings from different provenances in response to changed light intensities elicited significant differences in foliar photosynthesis among different provenances. The relationships between sensitivities and annual temperature difference, mean temperature in January, and mean annual evaporation of provenance were found to be the most closely related, which indicated that temperature range and effective precipitation of provenance were the main factors that affected photosynthetic plasticity of A. holophylla seedlings.References
Andrews S.F., Flanagan L.B., Sharp E.J., Cai T., 2012. Variation in water potential, hydraulic characteristics and water source use in montane Douglas-fir and lodgepole pine trees in southwestern Alberta and consequences for seasonal changes in photosynthetic capacity. Tree Physiology 32(2): 146-160. DOI: 10.1093/treephys/tpr136Aspinwall M.J., King J.S., McKeand S.E., Domec J.C., Whitehead D., 2011. Leaf-level gas-exchange uniformity and photosynthetic capacity among loblolly pine (Pinus taeda L.) genotypes of contrasting inherent genetic variation. Tree Physiology 31(1): 78-91. DOI: 10.1093/treephys/tpq107Babaei S.F., Jalali S.G., Sohrabi H., Shirvany A., 2014. Growth responses to irradiance regime along an ecological gradient of Quercus castaneifolia seedlings of different provenance. Ecological Research 29(2): 245-255. DOI: 10.1007/s11284-013-1119-9Carne D.J., 2013. A comparison of carbon sequestration potential and photosynthetic efficiency in evergreen and deciduous oaks growing in contrasting environments in the Southwest UK. Dissertation, University of Plymouth, Plymouth.Castanha C., Torn M.S., Germino M.J., Weibel B., Kueppers LM., 2013. Conifer seedling recruitment across a gradient from forest to alpine tundra: effects of species, provenance, and site. Plant Ecology & Diversity 6(3-4): 307-318. DOI: 10.1080/17550874.2012.716087Chong P.F., Su S.P., Gao M., Li Y., Sun Z.C., 2013. Comparative analysis on gas exchange characteristic of four geographical provenances of Nitraria tangutorum. Acta Prataculturae Sinica 22(2): 307-312. (In Chinese) Dinakar C., Djilianov D., Bartels D., 2012. Photosynthesis in desiccation tolerant plants: energy metabolism and antioxidative stress defense. Plant Science 182: 29-41. DOI: 10.1016/j.plantsci.2011.01.018Duan J., Xu C.Y., Jacobs D.F., Ma L.Y., Wei H.X., Jiang L.N., Ren J., 2013. Exponential nutrient loading shortens the cultural period of Larix olgensis seedlings. Scandinavian Journal of Forest Research 28(5): 409-418. DOI: 10.1080/02827581.2013.778328e Silva E.A.B., Hasegawa S.F., Ono K., Sumida A., Uemura S., Hara T., 2012. Differential photosynthetic characteristics between seedlings and saplings of Abies sachalinensis and Picea glehnii, in the field. Ecological Research 27(5): 933-943. DOI: 10.1007/s11284-012-0973-1Farquhar G.D., von Caemmerer S., Berry J.A., 1980. A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149(1): 78-90. DOI: 10.1007/BF00386231Flexas J., Diaz-Espejo A., Gago J., Gallé A., Galmésa J., Gulíasa J., Medranoa H., 2014. Photosynthetic limitations in Mediterranean plants: A review. Environmental and Experimental Botany 103: 12-23. DOI: 10.1016/j.envexpbot.2013.09.002Galmés J., Aranjuelo I., Medrano H., Flexas J., 2013. Variation in Rubisco content and activity under variable climatic factors. Photosynthesis Research 117(1-3): 73-90. DOI: 10.1007/s11120-013-9861-yGoldblum D., Kennett C., Lisowski A., 2012. Geographical variation in the photosynthesis characteristics of sugar maple (Acer saccharum) lab-and field-grown seedlings. Geographical Bulletin 53(2): 65-78.Jiang Z.R., Liang X.T., Zhu G., Song Y.P., Cong R.L., Wang S.X., Yang Q.Q., 2008. Sensitivity of three tree species reaction to seasonal variation and its relation to antistress ability. Journal of Northwest Forestry University 23(6): 46-49. (In Chinese)Jin X., Hu W.L., Kong X.W., Ding G.Q., Ding L., Xu QX., 2008. The effects of shading on the growth of Abies holophylla seedlings. Journal of Liaoning Forestry Science & Technology (1): 29-34. (In Chinese)Klein T., Di Matteo G., Rotenberg E., Cohen S., Yakir D., 2013. Differential ecophysiological response of a major Mediterranean pine species across a climatic gradient. Tree Physiology 33(1): 26-36. DOI: 10.1093/treephys/tps116Larcher W., 2003. Physiological plant ecology: ecophysiology and stress physiology of functional groups. Springer, Berlin. DOI: 10.1007/978-3-662-05214-3 Liu L.F., 2012. The Effects of Light on the nutrient absorption and partitioning of Abies holophylla seedlings. Dissertation, Beijing Forestry University, Beijing. (In Chinese)Mao Q.Z., Watanabe M., Imori M., Kim Y.S., Kita K., Koike T., 2012. Photosynthesis and nitrogen allocation in needles in the sun and shade crowns of hybrid larch saplings: effect of nitrogen application. Photosynthetica 50(3): 422-428. DOI: 10.1007/s11099-012-0049-zNasr Z., Khouja M.L., Aini R., Hammadi A., Manai H., Mimouni B., 2013. Ecophysiological performance of eight Jatropha curcas L. provenances cultivated in Tunisia. Journal of Applied Horticulture 15(2): 90-94.Okuto J.L., Ouma G., 2010. Provenance variation of photosynthesis of seedlings of java plum (S. cuminii) in Western Kenya. Agriculture & Biology Journal of North America 1(6): 1260-1263. DOI: 10.5251/abjna.2010.1.6.1260.1263Pan L., 2011 Study on dormancy release mechanisms of Abies holophylla Maxim. seed. Dissertation, Beijing Forestry University, Beijing. (In Chinese)Paquette A., Fontaine B., Berninger F., Dubois K., Lechowicz M.J., Messier C., Posada J.M., 2012. Norway maple displays greater seasonal growth and phenotypic plasticity to light than native sugar maple. Tree Physiology 32(11): 1339-1347. DOI: 10.1093/treephys/tps092Pérez-Ramos I.M., Gómez-Aparicio L., Villar R., García L.V., Mara-ón T., 2010. Seedling growth and morphology of three oak species along field resource gradients and seed mass variation: a seedling age-dependent response. Journal of Vegetation Science 21(3): 419-437. DOI: 10.1111/j.1654-1103.2009.01165.xReinhardt K., Castanha C., Germino M.J., Kueppers L.M., Pereira J., 2011. Ecophysiological variation in two provenances of Pinus flexilis seedlings across an elevation gradient from forest to alpine. Tree Physiology 31(6): 615-625. DOI: 10.1093/treephys/tpr055Rodríguez-García E., Bravo F., 2013. Plasticity in Pinus pinaster populations of diverse origins: Comparative seedling responses to light and Nitrogen availability. Forest Ecology and Management 307: 196-205. DOI: 10.1016/j.foreco.2013.06.046Shi H.J., Du F., Zhang X.C., 2010. Photosynthetic characteristic of some plant species in the Mu Us Desert. Journal of Northwest Forestry University 25(4): 29-34. (In Chinese)Song X.L., Yang H.Y., Zeng L.Q., Duan Y.Y., 2009. Study on the shading impact on plant. Northern Horticulture (5): 129-133. (In Chinese)Soustani F.B., Jalali S.G., Sohrabi H., Shirvany A., 2014. Growth responses to irradiance regime along an ecological gradient of Quercus castaneifolia seedlings of different provenance. Ecological Research 29(2): 245-255. DOI: 10.1007/s11284-013-1119-9Sun J.Y., Yang F.J., Pang H.H., Zhang X.K., Zu Y.G., 2007. Effects of shading treatment on photosynthetic response and life cycle form of Taxus chinensis var. mairei. Bulletin of Botanical Research 27(4): 439-444. (In Chinese)Sunil N., Vanaja M., Kumar V., Abraham B., Chakrabarty S.K., 2013. Variation in physiological traits in Jatropha germplasm from peninsular India. Indian Journal of Plant Physiology 18(2): 151-156. DOI: 10.1007/s40502-013-0026-yWang G.G., Bauerle W.L., Mudder B.T., 2006. Effects of light acclimation on the photosynthesis, growth, and biomass allocation in American chestnut (Castanea dentata) seedlings. Forest Ecology and Management 226(1): 173-180. DOI: 10.1016/j.foreco.2005.12.063Wientjes E., van Amerongen H., Croce R., 2013. Quantum yield of charge separation in photosystem II: functional effect of changes in the antenna size upon light acclimation. Journal of Physical Chemistry B 117(38): 11200-11208. DOI: 10.1021/jp401663wWyka T.P., Oleksyn J., Żytkowiak R., Karolewski P., Jagodziński A.M., Reich P.B., 2012. Responses of leaf structure and photosynthetic properties to intra-canopy light gradients: a common garden test with four broadleaf deciduous angiosperm and seven evergreen conifer tree species. Oecologia 170(1): 11-24. DOI: 10.1007/s00442-012-2279-yXu C.L., Sun X.M., Zhang S.G., 2012. Comparison in photosynthetic characteristics of Larix kaempferi, L. olgensis and their hybrids. Journal of Beijing Forestry University 34(4): 62-66. (In Chinese)Yao L., Wang Y., Ma J.F., Liu M.S., 2012. Discussion the effect on Abies holophylla canopy density to growth of natural regeneration seedling. Forestry Prospect and Design (1): 91-92. (In Chinese)Zhao X.Y., Ma K.F., Zhang M., Bian J.L., Jiao W.Y., Zhang Z.Y., 2011. Comparative analysis of the photosynthetic characteristics of three-year-old Populus tomentosa clones. Forest Research 24(3): 370-378. (In Chinese)Zhu X.G., Long S.P., Ort D.R., 2010. Improving photosynthetic efficiency for greater yield. Annual Review of Plant Biology 61: 235-261. DOI: 10.1146/annurev-arplant-042809-112206
Published
Issue
Section
License
All the papers published in Annals of Forest Research are available under an open access policy (Gratis Gold Open Access Licence), which guaranty the free (of taxes) and unlimited access, for anyone, to entire content of the all published articles. The users are free to “read, copy, distribute, print, search or refers to the full text of these articles”, as long they mention the source.
The other materials (texts, images, graphical elements presented on the Website) are protected by copyright.
The journal exerts a permanent quality check, based on an established protocol for publishing the manuscripts. The potential article to be published are evaluated (peer-review) by members of the Editorial Board or other collaborators with competences on the paper topics. The publishing of manuscript is free of charge, all the costs being supported by Forest Research and Management Institute.
More details about Open Access:
Wikipedia: http://en.wikipedia.org/wiki/Open_access