
两个乌桕新品种苗木光合特性比较
Comparison of photosynthetic characteristics of two new Triadica sebifera varieties
【目的】探讨两个乌桕新品种‘海滨绯红’、‘海滨紫晶’夏季光合特性并进行比较,为乌桕新品种的栽培与推广应用提供理论依据。【方法】盆栽条件下测定2年生嫁接苗叶片光合色素含量、光合日变化、光响应曲线以及CO2响应曲线,并进行灰色关联分析。【结果】① ‘海滨紫晶’的叶绿素a(Chla)、叶绿素b(Chlb)、类胡萝卜素(Car)含量以及叶绿素a/b(Chla/b)均高于‘海滨绯红’,其中叶绿素a、叶绿素b和类胡萝卜素含量存在显著性差异;② 两个品种8月光合日变化曲线皆为典型的单峰型,无“午休”现象,‘海滨紫晶’净光合速率(Pn)、气孔导度(Gs)和蒸腾速率(Tr)的日均值和峰值均显著高于‘海滨绯红’,而胞间CO2浓度(Ci)则相反;灰色关联分析表明,影响两个品种Pn的主要环境因子是大气温度(Ta)和光合有效辐射(PAR)。与‘海滨绯红’相比,‘海滨紫晶’的Pn与Ta的关联度更大,而与大气CO2浓度(Ca)关联度较小;③ ‘海滨紫晶’的最大净光合速率(Pn,max)、光饱和点(LSP)、暗呼吸速率(Rd)和光补偿点(LCP)均高于‘海滨绯红’,表观量子效率(AQY)低于‘绯红’,其中Pn,max、LSP和Rd存在显著性差异;④ ‘海滨紫晶’的最大光合能力(An,max)、CO2饱和点(CSP)、羧化效率(CE)和光呼吸速率(Rp)大于‘海滨绯红’,CO2补偿点(CCP)小于‘海滨绯红’,其中An,max、CSP存在显著性差异。【结论】两个乌桕新品种在光合特性上均表现出较强的夏季生长适应性。与‘海滨绯红’相比,‘海滨紫晶’光合性能较优,对高温及强光的适应性更强。其较强的光合能力与其在高温强光下所受的非气孔限制相对较小有关,较高的羧化效率和1,5-二磷酸核酮糖(RUBP)再生能力可能是‘海滨紫晶’改善非气孔限制的主要原因,光呼吸可能是其在高温强光下避免光抑制和光破坏的一种机制。
【Objective】The photosynthetic characteristics of two new Triadica sebifera varieties ‘Haibin Feihong’ (‘Feihong’) and ‘Haibin Zijing’ (‘Zijing’) in summer were studied and compared. This provided a theoretical basis for the cultivation and application of new T. sebifera varieties. 【Method】The photosynthetic pigment content, diurnal variation of photosynthesis, light response curve and CO2 response curve of 2-year-old grafted seedlings were measured under pot culture conditions, and a grey correlation analysis was conducted. 【Result】① The contents of chlorophyll a (Chl a), chlorophyll b (Chl b), carotenoid (Car) and chlorophyll a/b (Chl a/b) of ‘Zijing’ were all higher than that of ‘Feihong’, and the differences in Chl a, Chl b and Car content were significant. ② The diurnal variation curves of the photosynthesis of the two cultivars in August were a typical single peak type, and there was no ‘noon break’ phenomenon. The daily mean and peak values of the net photosynthetic rate (Pn), stomatal conductance (Gs) and transpiration rate (Tr) of ‘Zijing’ were significantly higher than those of ‘Feihong’, while the intercellular CO2 concentration (Ci) was the opposite. The grey correlation analysis showed that the main environmental factors affecting the two varieties of Pn were atmospheric temperature (Ta) and light intensity (PAR). Compared with ‘Feihong’, Pn was more related to Ta, but less to atmospheric CO2 concentration (Ca) in ‘Zijing’. ③ The maximum net photosynthetic rate (Pn,max), light saturation point (LSP), dark respiration rate (Rd) and light compensation point LCP) of ‘Zijing’ were all higher than those of the ‘Feihong’, and the apparent quantum efficiency (AQY) was lower than that of the ‘Feihong’, in which Pn,max, LSP and Rd were significantly different. ④ The maximum photosynthetic capacity (An,max), CO2 saturation point (CSP), carboxylation efficiency (CE) and light absorption rate (Rp) of the ‘Zijing’ were higher than those of ‘Feihong’, the CO2 compensation point (CCP) was smaller than that of the ‘Feihong’, and there were significant differences between An,max and CSP. 【Conclusion】The two new varieties of S. sebiferum showed strong adaptability to summer growth in terms of photosynthetic characteristics. Compared with ‘Feihong’, ‘Zijing’ had the best photosynthetic performance and better adaptability to high temperature and strong light. Its stronger photosynthetic capacity is related to its relatively small non-stomatal limitation. The higher carboxylation efficiency and RUBP regeneration ability may be the main reason for the improvement of non-stomatal limitation by ‘Zijing’. Photorespiration may be a mechanism to avoid light suppression and light destruction under high temperature and strong light.
乌桕新品种 / 光合日变化 / 光响应曲线 / CO2响应曲线
new varieties of Triadica sebifera / diurnal variation of photosynthesis / light response curve / CO2 response curve
[1] |
中国科学院中国植物志编辑委员会. 中国植物志[M]. 北京: 科学出版社, 2004.
Editorial Committee of Flora of China. Flora of China[M]. Beijing: Science Press, 2004.
|
[2] |
刘亚珍, 项瑶, 郭文锋, 等. 乌桕对南方根结线虫与地上不同食性昆虫互作的光合生理响应[J]. 植物保护, 2019,45(6):222-228.
|
[3] |
王文静, 董泰玮. 超声波辅助提取乌桕籽油的工艺优化研究[J]. 中国油脂, 2019,44(4):6-9.
|
[4] |
|
[5] |
张永丽, 潘其明, 张贵杰, 等. 山乌桕茎叶的化学成分研究[J]. 中国中药杂志, 2019,44(17):3738-3744.
|
[6] |
高莉, 田华, 吕培军, 等. 乌桕叶化学成分研究[J]. 中国中药杂志, 2015,40(8):1518-1522.
|
[7] |
董峰平. 乌桕EST-SSR标记开发与遗传评价[D]. 杭州:浙江农林大学, 2019.
|
[8] |
段亚豪, 曹玉玺, 吴祖芳, 等. 果酒酵母菌混合培养的生长规律及对山乌桕蜂蜜酒发酵风味分析[J]. 中国野生植物资源, 2019,38(05):36-42.
|
[9] |
史莹, 张丽珍, 曾志将, 等. 山乌桕蜂蜜酒酿造酵母的筛选、鉴定及应用[J]. 中国食品学报, 2013,13(10):197-204.
|
[10] |
Photosynthetic rate is concurrently limited by stomatal limitations and nonstomatal limitations (NSLs). However, the controls on NSLs to photosynthesis and their coordination with stomatal control on different timescales remain poorly understood. According to a recent optimization hypothesis, NSLs depend on leaf osmotic or water status and are coordinated with stomatal control so as to maximize leaf photosynthesis. Drought and notching experiments were conducted on Pinus sylvestris, Picea abies, Betula Pendula and Populus tremula seedlings in glasshouse conditions to study the dependence of NSLs on leaf osmotic and water status, and their coordination with stomatal control, on timescales of minutes and weeks, to test the assumptions and predictions of the optimization hypothesis. Both NSLs and stomatal conductance followed power-law functions of leaf osmotic concentration and leaf water potential. Moreover, stomatal conductance was proportional to the square root of soil-to-leaf hydraulic conductance, as predicted by the optimization hypothesis. Though the detailed mechanisms underlying the dependence of NSLs on leaf osmotic or water status lie outside the scope of this study, our results support the hypothesis that NSLs and stomatal control are coordinated to maximize leaf photosynthesis and allow the effect of NSLs to be included in models of tree gas-exchange.
|
[11] |
常恩福, 李娅, 李品荣, 等. 不同育苗基质对铁橡栎和乌桕苗木生长的影响[J]. 西部林业科学, 2018,47(3):56-62.
|
[12] |
|
[13] |
Drought is among the most damaging climate extremes, potentially causing significant decline in ecosystem functioning and services at the regional to global scale, thus monitoring of drought events is critically important. Solar-induced chlorophyll fluorescence (SIF) has been found to strongly correlate with gross primary production on the global scale. Recent advances in the remote sensing of SIF allow for large-scale, real-time estimation of photosynthesis using this relationship. However, several studies have used SIF to quantify the impact of drought with mixed results, and the leaf-level mechanisms linking SIF and photosynthesis are unclear, particularly how the relationship may change under drought. We conducted a drought experiment with 2-yr old Populus deltoides. We measured leaf-level gas exchange, SIF, and pulse amplitude modulated (PAM) fluorescence before and during the 1-month drought. We found clear responses of net photosynthesis and stomatal conductance to water stress, however, SIF showed a smaller response to drought. Net photosynthesis (Anet ) and conductance dropped 94% and 95% on average over the drought, while SIF values only decreased slightly (21%). Electron transport rate dropped 64% when compared to the control over the last week of drought, but the electron transport chain did not completely shut down as Anet approached zero. Additionally, SIF yield (SIFy ) was positively correlated with steady-state fluorescence (Fs ) and negatively correlated with non-photochemical quenching (NPQ; R(2) = 0.77). Both Fs and SIFy , after normalization by the minimum fluorescence from a dark-adapted sample (Fo ), showed a more pronounced drought response, although the results suggest the response is complicated by several factors. Leaf-level experiments can elucidate mechanisms behind large-scale remote sensing observations of ecosystem functioning. The value of SIF as an accurate estimator of photosynthesis may decrease during mild stress events of short duration, especially when the response is primarily stomatal and not fully coupled with the light reactions of photosynthesis. We discuss potential factors affecting the weak SIF response to drought, including upregulation of NPQ, change in internal leaf structure and chlorophyll concentration, and photorespiration. The results suggest that SIF is mainly controlled by the light reactions of photosynthesis, which operate on different timescales than the stomatal response.
|
[14] |
马迎莉, 高雨, 袁婷婷, 等. 重金属铬胁迫对髯毛箬竹光合特性的影响[J]. 南京林业大学学报(自然科学版), 2019,43(1):54-60.
|
[15] |
|
[16] |
苍晶, 赵会杰. 植物生理学实验教程[M]. 北京: 高等教育出版社, 2013:57-59.
|
[17] |
|
[18] |
叶子飘, 高峻. 光响应和CO2响应新模型在丹参中的应用[J]. 西北农林科技大学学报(自然科学版), 2009,37(1):129-134.
|
[19] |
The calculated maximum net photosynthetic rate (P N) at saturation irradiance (I m) of 1 314.13 μmol m−2 s−1 was 25.49 μmol(CO2) m−2 s−1, and intrinsic quantum yield at zero irradiance was 0.103. The results fitted by nonrectangular hyperbolic model, rectangular hyperbolic method, binomial regression method, and the new model were compared. The maximum P N values calculated by nonrectangular hyperbolic model and rectangular hyperbolic model were higher than the measured values, and the I m calculated by nonrectangular hyperbolic model and rectangular hyperbolic model were less than measured values. Results fitted by new model showed that the response curve of P N to I was nonlinear at low I for Oryza sativa, P N increased nonlinearly with I below saturation value. Above this value, P N decreased nonlinearly with I.
|
[20] |
Stressful environments such as salinity, drought, and high temperature (heat) cause alterations in a wide range of physiological, biochemical, and molecular processes in plants. Photosynthesis, the most fundamental and intricate physiological process in all green plants, is also severely affected in all its phases by such stresses. Since the mechanism of photosynthesis involves various components, including photosynthetic pigments and photosystems, the electron transport system, and CO2 reduction pathways, any damage at any level caused by a stress may reduce the overall photosynthetic capacity of a green plant. Details of the stress-induced damage and adverse effects on different types of pigments, photosystems, components of electron transport system, alterations in the activities of enzymes involved in the mechanism of photosynthesis, and changes in various gas exchange characteristics, particularly of agricultural plants, are considered in this review. In addition, we discussed also progress made during the last two decades in producing transgenic lines of different C3 crops with enhanced photosynthetic performance, which was reached by either the overexpression of C3 enzymes or transcription factors or the incorporation of genes encoding C4 enzymes into C3 plants. We also discussed critically a current, worldwide effort to identify signaling components, such as transcription factors and protein kinases, particularly mitogen-activated protein kinases (MAPKs) involved in stress adaptation in agricultural plants. |
[21] |
赵辉, 吕良贺, 路鑫, 等. 杂种金叶银杏叶片光合特性分析[J]. 南京林业大学学报(自然科学版), 2020,44(1):193-199.
|
[22] |
李春喜, 韩蕊, 邵云, 等. 小麦开花期旗叶光合特性与地上部干物质量的相关和通径分析[J]. 江苏农业科学, 2019,47(6):66-70.
|
[23] |
汤文华, 窦全琴, 潘平平, 等. 不同薄壳山核桃品种光合特性研究[J]. 南京林业大学学报(自然科学版), 2020,44(3):81-88.
|
[24] |
|
[25] |
|
[26] |
|
[27] |
叶子飘, 谢志亮, 段世华, 等. 设施栽培条件下三叶青叶片光合的气孔和非气孔限制[J]. 植物生理学报, 2020,56(1):41-48.
|
[28] |
Environmental stresses trigger a wide variety of plant responses, ranging from altered gene expression and cellular metabolism to changes in growth rates and crop yields. A plethora of plant reactions exist to circumvent the potentially harmful effects caused by a wide range of both abiotic and biotic stresses, including light, drought, salinity, high temperatures, and pathogen infections. Among the environmental stresses, drought stress is one of the most adverse factors of plant growth and productivity. Understanding the biochemical and molecular responses to drought is essential for a holistic perception of plant resistance mechanisms to water-limited conditions. Drought stress progressively decreases CO2 assimilation rates due to reduced stomatal conductance. Drought stress also induces reduction in the contents and activities of photosynthetic carbon reduction cycle enzymes, including the key enzyme, ribulose-1,5-bisphosphate carboxylase/oxygenase. The critical roles of proline and glycine-betaine, as well as the role of abscisic acid (ABA), under drought stress conditions have been actively researched to understand the tolerance of plants to dehydration. In addition, drought stress-induced generation of active oxygen species is well recognized at the cellular level and is tightly controlled at both the production and consumption levels in vivo, through increased antioxidative systems. Knowledge of sensing and signaling pathways, including ABA-mediated changes in response to drought stress, is essential to improve crop management. This review focuses on the ability and strategies of higher plants to respond and adapt to drought stress.
|
[29] |
吴志庄, 高贵宾, 熊德礼, 等. 9个主要丛生竹种光响应曲线的研究[J]. 竹子研究汇刊, 2013,32(2):16-20.
|
[30] |
Background: Over the past decades, the structural and functional genomics of rice have been deeply studied, and high density of molecular genetic markers have been developed. However, the genetic variation in leaf photosynthesis, the most important trait for rice yield improvement, was rarely studied. The lack of photosynthesis phenotyping tools is one of the bottlenecks, as traditional direct photosynthesis measurements are very low-throughput, and recently developed high-throughput methods are indirect measurements. Hence, there is an urgent need for a fast, accurate and direct measurement approach. Result: We reported a fast photosynthesis measurement (FPM) method for phenotyping photosynthetic capacity of rice, which measures photosynthesis of excised tillers in environment-controlled lab conditions. The light response curves measured using FPM approach coped well with that the curves measured using traditional gas exchange approach. Importantly, the FPM technique achieved an average throughput of 5.4 light response curves per hour, which was 3 times faster than the 1.8 light response curves per hour using the traditional method. Tillers sampled at early morning had the highest photosynthesis, stomatal conductance and the lowest variability. In addition, even 12 h after sampling, there was no significant difference of photosynthesis rate between excised tillers and in situ. We finally investigated the genetic variations of photosynthetic traits across 568 F2 lines using the FPM technique and discussed the logistics of screening several hundred samples per day per instrumental unit using FPM to generate a wealth of photosynthetic phenotypic data, which might help to improve the selection power in large populations of rice with the ultimate aim of improving yield through improved photosynthesis. Conclusions: Here we developed a high-throughput method that can measure the rice leaf photosynthetic capacity approximately 10 times faster than traditional gas exchange approaches. Importantly, this method can overcome measurement errors caused by environmental heterogeneity under field conditions, and it is possible to measure 12 or more hours per day under lab conditions.
|
[31] |
郑威, 何琴飞, 彭玉华, 等. 石漠化区6种退耕树种光响应曲线研究[J]. 中南林业科技大学学报, 2017,37(12):85-90.
|
[32] |
A modified exponential model was used to describe light-response curves of Nicotiana tabacum L. The accuracies of an exponential model, a nonrectangular hyperbola model, a rectangular hyperbola model, a modified rectangular hyperbola model and the modified exponential model were evaluated by Mean square error (MSE) and Mean absolute error (MAE). The tests MSE and MAE of the modified exponential model were the lowest among the five models. The light saturation point (LSP) obtained by the exponential model, the nonrectangular hyperbola model and the rectangular hyperbola model were much lower than the measured values, and the maximum net photosynthetic rates (P(max)) calculated from these models, were greater than the measured values. P(max) at LSP of 1,077 mu mol m(-2) s(-1) calculated by the modified exponential model was 12.34 mu mol(CO(2)) m(-2) s(-1), which was more accurate than the values obtained from the modified rectangular hyperbola model. The results show that the modified exponential model is superior to other models for describing light-response curves.
|
[33] |
|
[34] |
To clarify detailed characteristics of fruit photosynthesis, possible gas exchange pathway and photosynthetic response to different environments were investigated in Satsuma mandarin (Citrus unshiu). About 300 mm(-2) stomata were present on fruit surface during young stages ( approximately 10-30 mm diameter fruit) and each stoma increased in size until approximately 88 days after full bloom (DAFB), while the stomata collapsed steadily thereafter; more than 50% stomata deformed at 153 DAFB. The transpiration rate of the fruit appeared to match with stoma development and its intactness rather than the density. Gross photosynthetic rate of the rind increased gradually with increasing CO2 up to 500 ppm but decreased at higher concentrations, which may resemble C4 photosynthesis. In contrast, leaf photosynthesis increased constantly with CO2 increment. Although both fruit and leaf photosynthesis were accelerated by rising photosynthetic photon flux density (PPFD), fruit photosynthesis was greater under considerably lower PPFD from 13.5 to 68 mumolm(-2)s(-1). Thus, Satsuma mandarin fruit appears to incorporate CO2 through fully developed and non-collapsed stomata, and subject it to fruit photosynthesis, which may be characterized as intermediate status among C3, C4 and shade plant photosynthesis. The device of fruit photosynthesis may develop differently from its leaf to capture CO2 efficiently.
|
[35] |
Photosynthetic responses to carbon dioxide concentration can provide data on a number of important parameters related to leaf physiology. Methods for fitting a model to such data are briefly described. The method will fit the following parameters: V(cmax), J, TPU, R(d) and g(m)[maximum carboxylation rate allowed by ribulose 1.5-bisphosphate carboxylase/oxygenase (Rubisco), rate of photosynthetic electron transport (based on NADPH requirement), triose phosphate use, day respiration and mesophyll conductance, respectively]. The method requires at least five data pairs of net CO(2) assimilation (A) and [CO(2)] in the intercellular airspaces of the leaf (C(i)) and requires users to indicate the presumed limiting factor. The output is (1) calculated CO(2) partial pressure at the sites of carboxylation, C(c), (2) values for the five parameters at the measurement temperature and (3) values adjusted to 25 degrees C to facilitate comparisons. Fitting this model is a way of exploring leaf level photosynthesis. However, interpreting leaf level photosynthesis in terms of underlying biochemistry and biophysics is subject to assumptions that hold to a greater or lesser degree, a major assumption being that all parts of the leaf are behaving in the same way at each instant.
|
[36] |
刘杨杨, 李俊, 于强, 等. 甘蔗叶片光合CO2响应参数分析及其品种间差异[J]. 中国农业气象, 2019,40(10):637-646.
|
[37] |
李威, 杨德光, 牟尧, 等. 去遮荫后东北红豆杉幼苗和幼树光合特性对比[J]. 林业科学, 2018,54(2):179-185.
|
[38] |
Photorespiratory metabolism is essential for plants to maintain functional photosynthesis in an oxygen-containing environment. Because the oxygenation reaction of Rubisco is followed by the loss of previously fixed carbon, photorespiration is often considered a wasteful process and considerable efforts are aimed at minimizing the negative impact of photorespiration on the plant's carbon uptake. However, the photorespiratory pathway has also many positive aspects, as it is well integrated within other metabolic processes, such as nitrogen assimilation and C1 metabolism, and it is important for maintaining the redox balance of the plant. The overall effect of photorespiratory carbon loss on the net CO2 fixation of the plant is also strongly influenced by the physiology of the leaf related to CO2 diffusion. This review outlines the distinction between Rubisco oxygenation and photorespiratory CO2 release as a basis to evaluate the costs and benefits of photorespiration.
|
[39] |
何丽斯, 李辉, 刘晓青, 等. 基于光合特性评价10个杜鹃花品种的耐热能力[J]. 江苏林业科技, 2019,46(4):21-26.
|
/
〈 |
|
〉 |