胡杨异形叶光合作用对光强与CO2浓度的响应
收稿日期: 2014-05-30
录用日期: 2014-07-16
网络出版日期: 2021-04-20
基金资助
国家自然科学基金(30960033);国家自然科学基金(31260-058);中国科学院“西部之光”人才培养项目(RCPY 201209)
Photosynthetic responses of the heteromorphic leaves in Populus euphratica to light intensity and CO2concentration
Received date: 2014-05-30
Accepted date: 2014-07-16
Online published: 2021-04-20
胡杨(Populus euphratica)叶形多变, 随个体生长发育, 植株出现条形、卵形和锯齿阔卵形叶。在新疆塔里木河上游人工胡杨林内选择具有此3种叶形的成年标准株, 将枝条拉至同一高度, 通过活体测定, 比较其光合作用-光与CO2响应及叶绿素荧光响应特征。结果表明: 胡杨异形叶光合速率对光强/CO2浓度与电子传递速率对光强的响应曲线均可用直角双曲线修正模型来拟合, 得出的主要光合参数与实测值较吻合。胡杨卵形叶、锯齿阔卵形叶光合速率-光响应参数与生化参数及快速光响应参数与条形叶差异显著, 而光合速率-CO2响应参数则无显著差异。胡杨异形叶CO2饱和浓度下的最大净光合速率(Pnmax)较饱和光强下的Pnmax高, 表明胡杨强光下光合速率在很大程度上受CO2供应和1,5-二磷酸核酮糖(RuBP)再生能力的限制。卵形叶、锯齿阔卵形叶的初始量子效率(α)、初始羧化效率(CE)、Pnmax、光合能力(Amax)与最大羧化速率(Vcmax)均显著高于条形叶; 锯齿叶光饱和点(LSP)、最大电子传递速率(ETRmax)与光呼吸速率(Rp)高于卵形叶, 条形叶光补偿点(LCP)与LSP、α、CE最低。表明荒漠干旱环境下胡杨锯齿叶最耐强光, 高Rp可能是其耗散过剩光能、保护光合机构免于强光破坏的重要途径; 卵形叶高的α、CE、磷酸丙糖利用效率(TPU)、PSII实际光化学效率(ΦPSII)与低LCP及叶氮分配策略是其保持高光合速率的原因; 条形叶ΦPSII、ETR、Pn低, 因其制造光合产物不足而难以满足树体生长逐渐减少并处于树冠下部。可见, 胡杨条形叶光合效率低、抗逆性差, 主要以维持生长为主; 随着树体长大, 条形叶难以适应荒漠环境来维系其生长, 出现了卵形叶; 卵形叶光合效率高, 易于快速积累光合产物而加快树体生长, 但其LSP低和耐光抑制能力弱, 逐渐被更耐强光、高温与大气干旱的锯齿叶所取代, 从而使胡杨在极端逆境下得以生存, 这是胡杨从幼苗到成年叶形变化及异形叶着生在树冠不同高度的原因。
王海珍, 韩路, 徐雅丽, 牛建龙 . 胡杨异形叶光合作用对光强与CO2浓度的响应[J]. 植物生态学报, 2014 , 38(10) : 1099 -1109 . DOI: 10.3724/SP.J.1258.2014.00104
Aims Populus euphratica is an important tree species and its leaf shape changes along the growth stages. Adult trees commonly comprise polymorphic leaves, including lanceolate, oval and serrated broad-oval leaves. Our objective were to elucidate the ecophysiological mechanisms of P.euphratica adapting to high temperature and strong light environment and its survival strategy by comparing photosynthetic efficiency and chlorophyll fluorescence parameters in heteromorphic leaves in an extremely arid desert area, and to explore the causes of changes in leaf shape in P.euphratica, in order to provide a scientific basis for the protection of desert P.euphratica forests.
Methods Individuals with 10 cm diameter at breast height from a planted P.euphratica forest were selected. Measurements were made on the parameters of gas changes and chlorophyll fluorescence of three different leaf shapes on branches at the similar height using a LI-6400 Portable Photosynthesis System and a PAM-2100 chlorophyll fluorometer. The light/CO2 response curves of net photosynthetic rate (Pn) and rapid light curves of chlorophyll fluorescence in heteromorphic leaves were fitted and analyzed.
Important findings The light and CO2response curves, rapid light curves of the three different leaf shapes in P.euphraticawere better fitted by the modified rectangular hyperbola models, and the model values of key photosynthetic parameters were very close to the measured data. There were significant differences in the light responses, biochemical parameters and the parameters of rapid light curves among the oval, serrated broad-oval leaves and lanceolate leaves, but the heteromorphic leaves did not significantly differ in carbon assimilation efficiency. The maximum net photosynthetic rate (Pnmax) of the heteromorphic leaves under saturated intercellular CO2concentration was higher than under saturated irradiance, indicating that photosynthetic efficiency was limited to the great extent by CO2supply and regeneration rate of ribulose biphosphate (RuBP). Initial quantum yield (α), initial carboxylation efficiency (CE),Pnmax, photosynthetic capacity (Amax), maximum carboxylation rate (Vcmax) were greater in the oval and serrated broad-oval leaves than in the lanceolate leaves; the serrated broad-oval leaves had the highest light saturation point (LSP), photosynthetic electron transportation rate (ETRmax) and rate of photorespiration (Rp), whereas the lanceolate leaves had the lowest light compensation point (LCP), LSP, α and CE. All the results above indicate that the serrated broad-oval leaves having greater resistance to strong light and higher Rp may be an important mechanism for dissipating excessive light energy and protecting the photosynthetic apparatus from light damage. In contrast, the oval leaves had higher values in α, CE, triose-phosphate utilization efficiency (TPU), PSII actual photochemical efficiency (ΦPSII), leaf nitrogen allocation strategy and low LCP and therefore could maintain high photosynthetic rate in extremely arid areas. The lanceolate leaves had the lowest values in Pn, ΦPSII, and ETR, which would be difficult to meet the individual growth demand because of the low production of photosynthate, and their number declined with growth and distributed mainly toward the lower tree crowns.
| [1] | Albert KR, Mikkelsen TN, Michelsen A, Ro-Poulsen H, van der Linden L (2011). Interactive effects of drought elevated CO2and warming on photosynthetic capacity and photo system performance in temperate heath plants. Journal of Plant Physiology, 168,1550-1561. |
| [2] | Bai X, Zhang SJ, Zheng CX, Hao JQ, Li WH, Yang Y (2011). Comparative study on photosynthesis and water physiology of polymorphic leaves of Populus euphratica. Journal of Beijing Forestry University, 33(6),47-52. (in Chinese with English abstract) |
| [2] | [ 白雪, 张淑静, 郑彩霞, 郝建卿, 李文海, 杨扬 (2011). 胡杨多态叶光合和水分生理的比较. 北京林业大学学报, 33(6),47-52.] |
| [3] | Brodribb T, Hill RS (1997). Light response characteristics of a morphologically diverse group of southern hemisphere conifers as measured by chlorophyll fluorescence. Oecologia, 110,10-17. |
| [4] | Coste S, Roggy JC, Imbert P, Born C, Bonal D, Dreyer E (2005). Leaf photosynthetic traits of 14 tropical rain forest species in relation to leaf nitrogen concentration and shade tolerance. Tree Physiology, 25,1127-1137. |
| [5] | Demmig-Adams B, Adama III WW (1992). Photoprotection and other responses of plants to high light stress. Annual Review of Plant Physiology and Plant Molecular Biology, 43,599-626. |
| [6] | Deng X, Li XM, Zhang XM, Ye WH, Foezki A, Runge M (2003). The studies about the photosynthetic response of the four desert plants. Acta Ecologica Sinica, 23,598-605. |
| [7] | Farquhar GD, von Caemmerer S, Berry JA (1982). A biochemical model of photosynthetic CO2assimilation in leaves of C3species. Planta, 149,78-90. |
| [8] | Forcel L, Critchley C, van Rensen JS (2003). New fluorescence parameters for monitoring photosynthesis in plants. Photosynthesis Research, 78,17-33. |
| [9] | Guo LW, Shen YG (1996). Protective mechanisms against photo damage in photosynthetic apparatus of higher plants. Plant Physiology Communications, 32,1-8. (in Chinese with English abstract) |
| [9] | [ 郭连旺, 沈允钢 (1996). 高等植物光合机构避免强光破坏的保护机制. 植物生理学通讯, 32,1-8.] |
| [10] | Huang HY, Dou XY, Sun BY, Deng B, Wu GJ, Peng CL (2009). Comparison of photosynthetic characteristics in two ecotypes of Jatropha curcas in summer. Acta Ecologica Sinica, 29,2861-2867. (in Chinese with English abstract) |
| [10] | [ 黄红英, 窦新永, 孙蓓育, 邓斌, 吴国江, 彭长连 (2009). 两种不同生态型麻疯树夏季光合特性的比较. 生态学报, 29,2861-2867.] |
| [11] | Krause GH (1998). Photoinhibition of photosynthesis. An evaluation of damaging and protective mechanisms. Physiologia Plantarum, 74,566-574. |
| [12] | Lombardini L, Restrepo-Diaz H, Volder A (2009). Photosynthetic light response and epidermal characteristics of sun and shade pecan leaves. Journal of the American Society for Horticultural Science, 134,372-378. |
| [13] | Lu S, Zhang YQ, Wu B, Qin SG, Shen YB (2014). Measurement and simulation of photosynthesis-light response process in Artemisia ordosica under water stress. Journal of Beijing Forestry University, 36(1),55-61. (in Chinese with English abstract) |
| [13] | [ 鲁肃, 张宇清, 吴斌, 秦树高, 沈应柏 (2014). 水分胁迫下油蒿光合光响应过程及其模拟. 北京林业大学学报, 36(1),55-61.] |
| [14] | Ma HC, Fung L, Wang SS, Altman A, Hüttermann A (1997). Photosynthetic response of Populus euphratica to salt stress. Forest Ecology and Management, 93,55-61. |
| [15] | Maxwell K, Johnson GN (2000). Chlorophyll fluorescence―a practical guide. Journal of Experimental Botany, 51,659-668. |
| [16] | Schreiber U, Gademann R, Ralph PJ (1997). Assessment of photosynthetic performance of prochloron in Lissoclinum patella in Hospite by chlorophyll fluorescence measurements. Plant and Cell Physiology, 38,945-951. |
| [17] | Sofo A, Dichio B, Montanaro G, Xiliyannis C (2009). Photosynthetic performance and light response of two olive cultivars under different water and light regimes. Photosynthetica, 47,602-608. |
| [18] | Su PX, Zhang LX, Du MW, Bi YR, Zhao AF, Liu XM (2003). Photosynthetic character and water use efficiency of different leaf shapes of Populus euphratica and their response to CO2enrichment. Acta Phytoecologica Sinica, 27,34-40. (in Chinese with English abstract) |
| [18] | [ 苏培玺, 张立新, 杜明武, 毕玉蓉, 赵爱芬, 刘新民 (2003). 胡杨不同叶形光合特性、水分利用效率及其对加富CO2的响应. 植物生态学报, 27,34-40.] |
| [19] | Sun CX, Qi H, Hao JJ, Miao L, Wang J, Wang Y, Liu M, Chen LJ (2009). Single leaves photosynthetic characteristics of two insect-resistant transgenic cotton (Gossypium hirsutum L.) varieties in response to light. Photosynthctica, 47,399-408. |
| [20] | Tartachnyk II, Blanke MM (2004). Effect of delayed fruit har- vest on photosynthesis, transpiration and nutrient remobilization of apple leaves. New Phytologist, 164,441-450. |
| [21] | Tyree MC, Seiler JR, Maier CA, Johnsen KH (2009). Pinus taeda clones and soil nutrient availability: effects of soil organic matter incorporation and fertilization on biomass partitioning and leaf physiology. Tree Physiology, 29,1117-1131. |
| [22] | Wang HL, Yang SD, Zhang CL (1997). The photosynthetic characteristics of differently shaped leaves in Populus euphratica Olivier. Photosynthetica, 34,545-553. |
| [23] | Wang HZ, Han L, Xu YL, Wang L, Jia WS (2011). Response of chlorophyll fluorescence characteristics of Populus euphratica heteromorphic leaves to high temperature. Acta Ecologica Sinica, 31,2444-2453. (in Chinese with English abstract) |
| [23] | [ 王海珍, 韩路, 徐雅丽, 王琳, 贾文锁 (2011). 胡杨异形叶叶绿素荧光特性对高温的响应. 生态学报, 31,2444-2453.] |
| [24] | Wang RR, Xia JB, Yang JH, Zhao YY, Liu JT, Sun JK (2013). Comparison of light response models of photosynthesis in leaves of Periploca sepium under drought stress in sand habitat formed from seashells. Chinese Journal of Plant Ecology, 37,111-121. (in Chinese with English abstract) |
| [24] | [ 王荣荣, 夏江宝, 杨吉华, 赵艳云, 刘京涛, 孙景宽 (2013). 贝壳砂生境干旱胁迫下杠柳叶片光合光响应模型比较. 植物生态学报, 37,111-121.] |
| [25] | Wullschleger SD (1993). Biochemical limitations to carbon assimilation in C3 plants—a retrospective analysis of the A/Ci curves from 109 species. Journal of Experimental Botany, 44,907-920. |
| [26] | Xia JB, Zhang SY, Zhang GC, Xie WJ, Lu ZH (2011). Critical responses of photosynthetic efficiency in Campsis radicans (L.) Seem to soil water and light intensities. African Journal of Biotechnology, 10,17748-17754. |
| [27] | Ye ZP (2010). A review on modeling of responses of photosynthesis to light and CO2. Chinese Journal of Plant Ecology, 34,727-740. (in Chinese with English abstract) |
| [27] | [ 叶子飘 (2010). 光合作用对光和CO2响应模型的研究进展. 植物生态学报, 34,727-740.] |
| [28] | Ye ZP, Yu Q, Kang HJ (2012). Evaluation of photosynthetic electron flow using simultaneous measurements of gas exchange and chlorophyll fluorescence under photorespi-ratory conditions. Photosynthetica, 50,472-476. |
| [29] | Zhang GC, Xia JB, Shao HB, Zhang SY (2012). Grading woodland soil water productivity and soil bioavailability in the semi-arid Loess Plateau of China. Clean-Soil, Air, Water, 40,148-153. |
| [30] | Zhang YM, Zhou GS (2012). Advances in leaf maximum carboxylation rate and its response to environmental factors. Acta Ecologica Sinica, 32,5907-5917. (in Chinese with English abstract) |
| [30] | [ 张彦敏, 周广胜 (2012). 植物叶片最大羧化速率及其对环境因子响应的研究进展. 生态学报, 32,5907-5917.] |
/
| 〈 |
|
〉 |