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研究论文

增温对川西亚高山针叶林内不同光环境下红桦和岷江冷杉幼苗生长和生理的影响

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  • 1 中国科学院成都生物研究所,成都 610041
    2 四川省阿坝州川西林业局,四川阿坝州 623102

收稿日期: 2008-02-22

  录用日期: 2008-05-30

  网络出版日期: 2008-09-30

基金资助

国家自然科学基金重点项目(30530630);中国科学院西部行动计划重大项目(KZCX2-XB2-02);中国科学院知识创新工程重要方向项目(KSCX2-YW-N-066);西部之光人才计划项目

WARMING EFFECTS ON GROWTH AND PHYSIOLOGY OF SEEDLINGS OF BETULA ALBO-SINENSIS AND ABIES FAXONIANA UNDER TWO CONTRASTING LIGHT CONDITIONS IN SUBALPINE CONIFEROUS FOREST OF WESTERN SICHUAN, CHINA

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  • 1Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China
    2West Sichuan Forestry Bureau of Aba Tibetan and the Qiang People Autonomous Prefecture, Aba Prefecture, Sichuan 623102, China

Received date: 2008-02-22

  Accepted date: 2008-05-30

  Online published: 2008-09-30

摘要

川西亚高山针叶林是青藏高原东部高寒林区的重要组成部分, 也是研究全球变化对森林生态系统影响的重要森林类型。开展亚高山针叶林不同树种对气候变暖响应差异的研究, 可为预测未来气候变暖背景下亚高山针叶林植被组成和森林动态提供科学依据。我们以川西亚高山针叶林两种主要树种——红桦(Betula albo-sinensis)和岷江冷杉(Abies faxoniana)为研究材料, 采用开顶式增温法(Open-top chamber, OTC)模拟气候变暖, 研究了增温对全光条件和林下低光环境中(约为全光的10%)生长的红桦和岷江冷杉幼苗生长和生理的影响。在人工林环境下, OTC使增温框内平均气温和地表温度分别升高了0.51和0.33 ℃; 而在林外空地处, OTC使二者分别升高了0.69和0.41 ℃。研究结果显示, 增温总体上促进了两种幼苗的生长和生理过程, 并促使幼苗将更多的生物量投入到其同化部位——叶, 使幼苗的根冠比(R/S)显著降低。增温通过增加叶片的光合色素含量和表观量子效率等光合参数, 促进了幼苗的光合过程和生长。然而, 增温对两种幼苗生长和生理的影响效果与植物种类及其所处的光环境有关。增温仅在林外全光条件下显著影响红桦幼苗的生长和生理过程。岷江冷杉幼苗对增温的响应与红桦相反, 即增温仅在林下低光环境下对岷江冷杉幼苗的生长和生理过程有明显促进作用。这种响应差异可能赋予这两种植物在未来气候变暖背景下面对外界环境变化时具有不同的适应能力和竞争优势, 从而对亚高山针叶林生态系统物种组成和森林动态产生潜在影响。

本文引用格式

尹华军, 赖挺, 程新颖, 蒋先敏, 刘庆 . 增温对川西亚高山针叶林内不同光环境下红桦和岷江冷杉幼苗生长和生理的影响[J]. 植物生态学报, 2008 , 32(5) : 1072 -1083 . DOI: 10.3773/j.issn.1005-264x.2008.05.012

Abstract

Aims The subalpine coniferous forests in eastern Qinghai-Tibet Plateau provide a natural laboratory for studying effects of climate warming on terrestrial ecosystems. Research on differences between tree species in their responses to experimental warming can provide insights into their regeneration behavior and community composition under a future warmer climate.

Methods We used open-top chamber (OTC) to determine short-term effects of two levels of air temperature (ambient and warmed) and light (full light and ca. 10% of full light regimes) on the early growth and physiology of Betula albo-sinensis and Abies faxonianaseedlings.

Important findings The OTC manipulation increased mean air temperature and soil surface temperature by 0.51 ℃ and 0.33 ℃, respectively, under the 60-year plantation and 0.69 ℃ and 0.41 ℃, respectively, under the forest opening. Warming generally increased the growth, biomass accumulation and advanced physiological processes for seedlings of both species. In response to warming, both species allocated relatively more biomass to foliage and had significantly decreased root/shoot ratios (R/S), which might provide tree species an adaptive advantage when other environmental factors are not limiting. Warming may enhance photosynthesis in the two seedlings by increasing efficiency of PSⅡ in terms of increase inFv/Fm, photosynthetic pigment concentrations and apparent quantum yield (Φ). However, the effects of warming on seedling growth and physiological performance varied by light conditions and species. For B. albo-sinensis seedlings, the effects of warming were pronounced only under full-light conditions, while the growth and physiological responses of A. faxoniana seedlings to warming were found only under low-light conditions. Competitive and adaptive relationships between the two species may be altered as a result of response differences to warming manipulation. The short-term beneficial impact of warming on the early growth and development of the two species suggests that global warming may lead to changes in regeneration dynamics and species composition in subalpine coniferous forest ecosystems.

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参考文献

[1] Aerts R, Cornelissen JHC, Dorrepaal E (2006). Plant performance in a warmer world: general responses of plants from cold, northern biomes and the importance of winter and spring events. Plant Ecology, 182,65-77.
[2] Aiken RM, Smucker AJM (1996). Root system regulation of whole plant growth. Review of Phytopathology, 25,325-346.
[3] Awada T, Radoglou K, Fotelli MN, Constantinidou HIA (2003). Ecophysiology of seedlings of three Mediterranean pine species in contrasting light regimes. Tree Physiology, 23,33-41.
[4] Bilger W, Fisahn J, Brummet W (1995). Violaxanthin cycle pigment contents in potato and tobacco plants with genetically reduced photosynthetic capacity. Plant Physiology, 108,1479-1486.
[5] Bj?rkman O (1981). Responses to different quantum flux densities. In: Lange OL, Nobe PS, Ziegler Heds. Encyclopedia of Plant Physiology. Springer-Verlag, Berlin,57-106.
[6] Cai TB, Dang QL (2002). Effects of soil temperature on parameters for a coupled photosynthesis-stomatal conductance model. Tree Physiology, 22,819-829.
[7] Camm EL, Harper GJ (1991). Temporal variations in cold sensitivity of root growth in cold-stored white spruce seedlings. Tree Physiology, 9,425-431.
[8] Cornelissen JHC, Castro Diez P, Hunt R (1996). Seedling growth, allocation and leaf attributes in a wide range of woody plant species and types. Journal of Ecology, 84,755-765.
[9] Danby RK, Hik DS (2007). Responses of white spruce ( Picea glauca) to experimental warming at a subarctic alpine treeline. Global Change Biology, 13,437-451.
[10] Domisch T, Finér L, Lehto T (2002). Growth, carbohydrate and nutrient allocation of Scots pine seedlings after exposure to simulated low soil temperature in spring. Plant and Soil, 246,75-86.
[11] Havranek WM, Tranquillini W (1995). Physiological processes during winter dormancy and their ecological significance. In: Smith WK, Hinckley TM eds. Ecophysiology of Coniferous Forests. Academic Press, San Diego, CA, USA, 95-124.
[12] Hirose T, Werger MJA (1987). Nitrogen use efficiency in instantaneous and daily photosynthesis of leaves in the canopy of a Solodago alissima stand. Physiologia Plantarum, 70,215-222.
[13] Hollister RD, Webber PJ (2000). Biotic validation of small open-top chambers in a tundra ecosystem. Global Change Biology, 6,835-842.
[14] IPCC Intergovernmental Panel on Climate Change (2007). Contribution of working group Ⅲ to the fourth assessment report of the intergovernmental panel on climate change. In: Metz B, Davidson OR, Bosch PR, Dave R, Meyer LA eds. Climate Change in 2007: Mitigation. Cambridge University Press, Cambridge, UK.
[15] Kauppi P, Posch M (1985). Sensitivity of boreal forests to possible climatic warming. Climatic Change, 7,45-54.
[16] Kennedy AD (1995). Simulated climate change: are passive greenhouses a valid microcosm for testing the biological effects of environmental perturbations? Global Change Biology, 1,29-42.
[17] Kolek J, Kozinka V (1991). Physiology of the Plant Root System. Kluwer Academic Publishers, Dordrecht, 26.
[18] Krause GH, Weis E (1991). Chlorophyll fluorescence and photosynthesis: the basics. Annual Review of Plant Physiology and Plant Molecular Biology, 42,313-349.
[19] Kullman L (2002). Rapid recent range-margin rise of tree and shrub species in the Swedish Scandes. Journal of Ecology, 90,68-77.
[20] Lewis JD, Olszyk D, Tingey DT (1999). Seasonal patterns of photosynthetic light responses in Douglas-fir seedlings subjected to elevated atmospheric CO 2 and temperature. Tree Physiology, 19,243-252.
[21] Lichtenthaler HK (1987). Chlorophylls and carotenoids:pigments of photosynthetic biomembranes. In: Colowick SP, Kaplan NO eds. Methods in Enzymology. Academic Press, New York, 350-381.
[22] Liu Q (刘庆) (2002). Ecological Research on Subalpine Coniferous Forests in China(亚高山针叶林生态学研究). Sichuan University Press,Chengdu. (in Chinese)
[23] Liu XD, Chen BD (2000). Climatic warming in the Tibetan Plateau during recent decades. International Journal of Climatology, 20,1729-1742.
[24] Lloret F, Pe?uelas J, Estiarte M (2004). Experimental evidence of reduced diversity of seedlings due to climate modification in a Mediterranean-type community. Global Change Biology, 10,248-258.
[25] Lopushinsky W, Max TA (1990). Effect of soil temperature on root and shoot growth and on budburst timing in conifer seedling transplants. New Forests, 4,107-124.
[26] Marion GM, Henry GHR, Freckman DW, Johstone J, Jones G, Jones MH, Levesque E, Molau U, Parsons AN, Svoboda J, Virginia RA (1997). Open-top designs for manipulating field temperature in high-latitude ecosystems. Global Change Biology, 3 (Suppl. 1),20-30.
[27] Maxwell K, Johnson GN (2000). Chlorophyll fluorescence—a practical guide. Journal of Experimental Botany, 51,659-668.
[28] Mitchell AK, Arnott JT (1995). Effects of shade on the morphology and physiology of amabilis fir and western hemlock seedlings. New Forests, 10,79-98.
[29] Mortensen LV (1994). Effect of carbon dioxide concentration on assimilation partitioning, photosynthesis and transpiration of Betula pendula. Roth and Picea abies (L.) Karst. seedlings at two temperatures. Acta Agriculturae Scandinavica Section B-Soil and Plant Science, 44,164-169.
[30] Ormrod D, Lesser VM, Olszyk DM, Tingey DT (1999). Elevated temperature and carbon dioxide affect chlorophyll and carotenoids in Douglas-fir seedlings. International Journal of Plant Sciences, 160,529-534.
[31] Saxe H, Cannel MGR, Johnsen O, Ryan MG, Vourlitis G (1998). Tree and forest functioning in an enriched CO 2 atmosphere. New Phytologist, 139,369-400.
[32] Taiz L, Zeiger E (1998). Plant Physiology 2nd edn.Sinauer Associates Inc. Publishers, Sunderland, Massachusetts, USA, 518.
[33] Usami T, Lee J, Oikawa T (2001). Interactive effects of increased temperature and CO 2 on the growth of Quercus myrsinaefolia saplings. Plant, Cell and Environment, 24,1007-1019.
[34] Wang KY, Kellom?ki S, Zha T (2003). Modifications in photosynthetic pigments and chlorophyll fluorescence in 20-year-old pine trees after a four-year exposure to carbon dioxide and temperature elevation. Photosynthetica, 41,167-175.
[35] Yin HJ (尹华军), Liu Q (刘庆) (2005). Seed rain and soil seed banks of Picea asperata in subalpine spruce forests, western Sichuan, China. Acta Phytoecologica Sinica (植物生态学报), 29,108-115. (in Chinese with English abstract)
[36] Yin HJ, Liu Q, Lai T (2008). Warming effects on growth and physiology in the seedlings of the two conifers Picea asperata and Abies faxoniana under two contrasting light conditions. Ecological Research, 23,459-469.
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