镉胁迫对草莓光合的影响

通过盆栽试验,研究了Cd胁迫对草莓叶片叶绿素含量、光合速率、气孔导度、蒸腾速率和胞间二氧化碳浓度的影响.结果表明,Cd降低草莓叶片中的叶绿素总量,并改变叶绿素a和叶绿素b的比例;Cd降低草莓叶的光合速率和气孔导度,但在Cd胁迫初期,低浓度的Cd对草莓叶的光合速率和气孔导度有促进作用;Cd还降低草莓叶片的蒸腾速率和胞间CO₂浓度,其中,胞间CO₂浓度的降低幅度相对较小.     

黄连木对干旱胁迫的生理响应

研究了自然干旱条件下黄连木（Pistacia chinensis Bunge）的生理变化。结果表明,随土壤含水量的减少,叶绿素b含量、光合速率、叶片相对含水量与叶水势均下降;叶绿素a和可溶性糖含量、叶绿素a和b的比值及总叶绿素含量呈现上升的趋势;超氧化物歧化酶活性先升后降;丙二醛含量干旱胁迫前期升高,后期变化不明显;净光合速率、气孔导度和蒸腾速率随土壤含水量的减少逐步降低。气孔和可溶性糖含量都是影响黄连木光合速率的关键因子,干旱胁迫前12d光合速率主要受气孔限制,之后为非气孔限制。干旱胁迫前期渗透调节物质以可溶性糖为主,干旱胁迫较重时脯氨酸含量急剧升高,与可溶性糖同时起渗透调节作用。     

模拟大气硫酸铵污染对香樟幼苗生长及光合特性的影响

通过室内盆栽实验研究了大气颗粒污染物硫酸铵对香樟幼苗生长及光合特性的影响。结果表明,香樟幼苗叶片涂抹硫酸铵处理对植物生长无显著影响;低浓度硫酸铵(2 g·L^-1)提高了叶片叶绿素含量,而高浓度(4 g·L^-1)却降低了叶片叶绿素含量;与对照相比,低浓度处理的香樟叶片净光合速率、气孔导度、胞间二氧化碳浓度与蒸腾速率无显著差异;高浓度处理的香樟叶片净光合速率与蒸腾速率高于对照,而气孔导度与胞间二氧化碳浓度与对照无显著差异。机理分析表明,硫酸铵颗粒物主要通过影响叶片气孔导度来影响植物光合特性。     

水杨酸和茉莉酸甲酯对丹参幼苗叶片显微结构、光合及非结构糖积累的影响

研究了水杨酸(SA)和茉莉酸甲酯(MeJA)处理对丹参(Salvia miltiorrhiza Bunge)幼苗叶片显微结构、叶片光合能力及幼苗中非结构糖积累的影响.结果显示:SA处理增加了丹参幼苗叶片气孔密度;叶肉细胞排列紧密、体积减小,叶肉细胞内叶绿体数目减少,但叶绿体体积增大,叶绿体基粒片层结构的数目增加;叶片中叶绿素a、b含量、叶气孔导度、蒸腾速率以及净光合速率均增加;同时,幼苗根中和叶片中酸性转化酶活性降低,幼苗地上部分蔗糖含量及可溶性糖总量显著高于对照.MeJA处理减少了叶片气孔密度,气孔发育畸形;叶肉细胞间隙增大,栅栏细胞层数减少,叶肉细胞内叶绿体数目减少,叶绿体体积减小,叶绿体基粒片层结构被破坏;叶片中叶绿素a及类胡萝卜素含量、叶片的净光合速率低于对照,叶气孔导度、蒸腾速率增强;同时,幼苗根中及叶中酸性转化酶活性增加,幼苗根中蔗糖含量及可溶性糖总量显著低于对照.可见,SA处理能促进植物叶片显微结构发育,增强叶片光合能力,抑制蔗糖降解并促进蔗糖积累;而MeJA处理则破坏了植物叶片显微结构,降低了叶片光合能力,促进了蔗糖降解并减少蔗糖积累.     

水分胁迫对小麦叶片光合作用的影响及其与抗旱性的关系

在水分胁迫初期,两个小麦品种叶片光合速率,气孔导度和细胞间隙CO_2浓度降低,气孔限制值增加,光合速率的降低主要是气孔因素的限制。中度到严重水分胁迫使叶片光合速率、气孔导度和气孔限制值降低,细胞间隙CO_2浓度明显增加,且叶圆片放氧能力,叶绿体Hill反应、叶绿素荧光强度和表观量子产额降低,此时光合速率的降低主要是叶肉细胞光合活性的下降引起的。抗旱性弱的郑引一号叶肉细胞光合活性比抗旱性强的丰抗13更容易受到水分胁迫的影响。     

不同蚕豆品种对铅污染的光合生理响应特征

以3个蚕豆品种(分别为K0883、K0502、K0697)为试验材料,通过大田模拟小剂量Pb污染(浓度为40和250 mg·kg^-1),研究了净光合速率、气孔导度、蒸腾速率、细胞间隙CO₂浓度、水分利用效率、叶绿素含量等光合生理响应特征的变化在不同品种中的差异.结果表明,Pb污染下3个蚕豆品种气孔导度和蒸腾速率没有显著变化,叶绿素含量有不同程度的上升;在250 mg·kg^-1 Pb浓度下,K0883蚕豆品种净光合速率、水分利用效率、细胞间隙CO₂浓度分别升高121.80％、上升193.70％、下降42.76％.3个蚕豆品种对Pb污染的抗性大小顺序为K0883＞K0697＞K0502.蚕豆不同光合生理指标对小剂量Pb污染的响应特征不同.不同蚕豆品种对小剂量Pb污染的响应特征存在差异,这种种内的差异性采用单个生理指标难以反映,只有通过对多个指标的整合分析才能表现出来.     

NaCl胁迫抑制玉米幼苗光合作用的可能机理

用NaCl 100mmol/L处理玉米幼苗,216 h内不同时间分别测叶片光合速率及其它生理指标,结果表明随处理时间的延长,光合速率下降,气孔导度减小,细胞间隙CO2浓度先降低后升高(图1);叶片MDA(图5a)、Cl-、Pi(图4)及可溶性糖(图2b)含量增加;质膜透性增大(图2a);Chla/Chl b(图3b)及Fv/Fm(图5b)减小;MDH、PEPC酶活性降低(图6).细胞间隙CO2浓度的变化,说明光合速率下降的原因短时间内以渗透胁迫产生的气孔限制因素为主,长时间时以非气孔因素为主.Cl-多对细胞产生离子毒害,Pi的增多可竞争性地抑制RuBP羧化酶的活性.MDA的增加表明活性氧增多,活性氧通过使酶失活和膜伤害抑制细胞生长,使细胞内糖利用减少,可溶性糖含量增加,进而反馈性地抑制光合作用.活性氧还可以漂白叶绿素、增强光抑制及使与光合作用有关的酶失活,而抑制光合作用.因此,NaCl胁迫下光合作用降低的原因是多因素共同作用的结果,短时间内以气孔限制因素为主,长时间时以非气孔因素为主,在非气孔因素中活性氧的增加是主导因素.     

脱硫废弃物对盐碱地水稻幼苗生理特性的影响

以 '96-D10'水稻品种为材料,测定了不同脱硫废弃物施用量下盐碱地水稻幼苗光合作用和相关生理指标的变化,以探讨脱硫废弃物对水稻生长影响的生理机制.结果表明,施用适量的脱硫渣能显著增加水稻幼苗的根长、株高和生物量;适量的脱硫废弃物能使水稻叶片的净光合速率、气孔导度、气孔限制值、蒸腾速率和水分利用效率均较对照有显著增加,而细胞间隙CO2浓度比对照显著降低;施用适量的脱硫废弃物还能显著提高水稻叶片叶绿素含量,增加脯氨酸和可溶性糖的积累.研究发现,施用适量(22.5 t/hm2)脱硫废弃物能有效改善盐碱地水稻幼苗的光合作用,增强其渗透调节物质的积累,从而显著促进幼苗生长.     

水稻矮杆多分蘖突变体CA648的光合生理特性分析

本研究分析了水稻矮杆多分蘖突变体丛矮648 (CA648)及对照中花11 (ZH11)在分蘖期叶片的叶绿素含量、光合速率,还原糖、蔗糖含量以及POD酶活力。结果表明,分蘖期ZH11剑叶中叶绿素含量高于CA648。水稻分蘖前期,CA648的净光合速率、气孔导度、蒸腾速率都低于ZH11,胞间CO2浓度高于ZH11;而在分蘖盛期(分蘖期后20 d)两种材料的净光合速率差异显著,ZH11净光合速率比CA648高17.5%,同时CA648的气孔导度、胞间CO2浓度和蒸腾速率都低于ZH11;而分蘖后期ZH11与CA648净光合速率几乎相同。分蘖盛期CA648叶片还原糖含量明显比对照高;而茎杆还原糖含量与对照无差异。CA648叶片蔗糖含量低于对照,约为ZH11的77.5%;而茎杆的蔗糖含量高于对照,比ZH11高30.7%。两种材料POD酶活力差异明显,其中在分蘖盛期,CA648叶、茎中的POD酶活力分别比ZH11高73.0%、16.8%。     

我国1950s～1990s推广的玉米品种叶片

自1950s以来,我国玉米（Zea maysL.）产量以年递增幅度为126kg.hm-2.a-1的速率迅速提高。在高肥力自然光照条件下,通过对我国1950s、1970s、1990s等3个年代玉米主要推广品种的光合特性研究表明：当代品种叶片光合速率高且高值持续期长,光合色素叶绿素a、叶绿素b、类胡萝卜素等的含量高且持续时间长,与光合有关的蒸腾速率（E）、细胞间隙CO2浓度（Ci）、气孔导度（gs）等也有较大改良,中下部叶片尤其明显;在生育后期,当代品种具有更高的光合优势。在品种更替过程中光合色素的组成比率没有显著变化,随品种更替生育后期当代品种细胞间隙CO2浓度低的原因不是气孔限制,而是叶片同化CO2能力增强的结果。我国玉米产量的大幅度提高在很大程度上应归功于叶片光合性能的改良。     

Mechanisms and ecological consequences of plant defence induction and suppression in herbivore communities

Background Plants are hotbeds for parasites such as arthropod herbivores, which acquire nutrients and energy from their hosts in order to grow and reproduce. Hence plants are selected to evolve resistance, which in turn selects for herbivores that can cope with this resistance. To preserve their fitness when attacked by herbivores, plants can employ complex strategies that include reallocation of resources and the production of defensive metabolites and structures. Plant defences can be either prefabricated or be produced only upon attack. Those that are ready-made are referred to as constitutive defences. Some constitutive defences are operational at any time while others require activation. Defences produced only when herbivores are present are referred to as induced defences. These can be established via de novo biosynthesis of defensive substances or via modifications of prefabricated substances and consequently these are active only when needed. Inducibility of defence may serve to save energy and to prevent self-intoxication but also implies that there is a delay in these defences becoming operational. Induced defences can be characterized by alterations in plant morphology and molecular chemistry and are associated with a decrease in herbivore performance. These alterations are set in motion by signals generated by herbivores. Finally, a subset of induced metabolites are released into the air as volatiles and function as a beacon for foraging natural enemies searching for prey, and this is referred to as induced indirect defence.Scope The objective of this review is to evaluate (1) which strategies plants have evolved to cope with herbivores and (2) which traits herbivores have evolved that enable them to counter these defences. The primary focus is on the induction and suppression of plant defences and the review outlines how the palette of traits that determine induction/suppression of, and resistance/susceptibility of herbivores to, plant defences can give rise to exploitative competition and facilitation within ecological communities “inhabiting” a plant.Conclusions Herbivores have evolved diverse strategies, which are not mutually exclusive, to decrease the negative effects of plant defences in order to maximize the conversion of plant material into offspring. Numerous adaptations have been found in herbivores, enabling them to dismantle or bypass defensive barriers, to avoid tissues with relatively high levels of defensive chemicals or to metabolize these chemicals once ingested. In addition, some herbivores interfere with the onset or completion of induced plant defences, resulting in the plant’s resistance being partly or fully suppressed. The ability to suppress induced plant defences appears to occur across plant parasites from different kingdoms, including herbivorous arthropods, and there is remarkable diversity in suppression mechanisms. Suppression may strongly affect the structure of the food web, because the ability to suppress the activation of defences of a communal host may facilitate competitors, whereas the ability of a herbivore to cope with activated plant defences will not. Further characterization of the mechanisms and traits that give rise to suppression of plant defences will enable us to determine their role in shaping direct and indirect interactions in food webs and the extent to which these determine the coexistence and persistence of species.     

Relative growth rate, biomass allocation pattern and water use efficiency of three wheat cultivars during early ontogeny as dependent on water availability

We have investigated the water use efficiency of whole plants and selected leaves and allocation patterns of three wheat cultivars (Mexipak, Nesser and Katya) to explore how variation in these traits can contribute to the ability to grow in dry environments. The cultivars exhibited considerable differences in biomass allocation and water use efficiency. Cultivars with higher growth rates of roots and higher proportions of biomass in roots (Nesser and Katya) also had higher leaf growth rates, higher proportions of their biomass as leaves and higher leaf area ratios. These same cultivars had lower rates of transpiration per unit leaf area or unit root weight and higher biomass production per unit water use. They also had higher ratios of photosynthesis to transpiration, and lower ratios of intercellular to external CO₂ partial pressure. The latter resulted from large differences in stomatal conductance associated with relatively small differences in rates of photosynthesis. There was little variation between cultivars in response to drought, and differences in allocation pattern and plant water use efficiency between cultivars as found under well-watered conditions persisted under dry conditions. At the end of the non-watered treatment, relative growth rates and transpiration rates decreased to similar values for all cultivars. High ratios of photosynthesis to transpiration, and accordingly high biomass production per unit of transpiration, is regarded as a favourable trait for dry environments, since more efficient use of water postpones the decrease in plant water status.     

Striga hermonthica reduces photosynthesis in sorghum: the importance of stomatal limitations and a potential role for ABA?

We report the effects of the root hemiparasite Striga hermonthica (Del.) Benth. on the growth and photosynthesis of two cultivars of sorghum: CSH-1, a susceptible variety, and Ochuti, which shows some tolerance to S. hermonthica in the field. Within 4 d of parasite attachment to the host roots, infected plants of both cultivars were significantly shorter than uninfected controls. At 55 d, infected plants of both cultivars had significantly less shoot and root biomass, and significantly smaller leaf areas than uninfected controls. The dry weight of S. hermonthica attached to host roots was insufficient at this stage to explain the decreased growth in terms of a competing sink for carbon and nitrogen. Leaf chlorophyll and nitrogen per unit area were greater in infected plants of both cultivars compared with control plants. However, whereas photosynthesis and transpiration in young leaves of infected CSH-1 plants declined with time when compared with controls, the rates in infected Ochuti plants were similar to those in uninfected controls throughout the time course of observation. In both cultivars, a strong correlation was observed between the rate of photosynthesis and stomatal conductance during photosynthetic induction, but infection resulted in a much slower induction than in controls. In CSH-1 plants, both steady-state photosynthesis and stomatal conductance were lower than in controls, whereas in leaves of Ochuti steady-state photosynthesis and stomatal conductance eventually reached the same values as in the control leaves. Results from AlC_i analysis and also from determination of ¹³C isotope discrimination were consistent with a stomatal limitation to photosynthesis in the leaves of Striga-infected plants. The concentration of the plant growth regulator abscisic acid (ABA) was measured in the xylem sap of infected CSH-1 plants only, and was found to be twice that of uninfected plants. A possible role of ABA in determining host response to infection by S. hermonthica is discussed.     

The efficiency of water use in water stressed plants is increased due to ABA induced stomatal closure

Gas exchange and abscisic acid content of Digitalis lanata EHRH. have been examined at different levels of plant water stress. Net photosynthesis, transpiration and conductance of attached leaves declined rapidly at first, then more slowly following the withholding of irrigation. The intercellular partial pressure of CO₂ decreased slightly. The concentration of 2-cis(S)ABA increased about eight-fold in the leaves of non-irrigated plants as compared with well-watered controls. A close linear correlation was found between the ABA content of the leaves and their conductance on a leaf area basis. In contrast, the plot of net assimilation versus ABA concentration was curvilinear, leading to an increased efficiency of water use during stress. After rewatering, photosynthesis reached control values earlier than transpiration, leaf conductance and ABA content. From these data it is concluded that transpiration through the stomata is directly controlled by the ABA content, whereas net photosynthesis is influenced additionally by other factors.Possible reasons for the responses of photosynthesis and water use efficiency to different stress and ABA levels are discussed.Abbreviations A net CO₂ assimilation - ABA abscisic acid - C_i intercellular CO₂ concentration - g stomatal conductance - T transpiration - WUE water use efficiency     

中国北方杂草稻光合与水分生理特性

杂草稻是一类重要的稻属种质资源,具有耐寒、耐旱、耐瘠薄等优良特性.本文以88份中国北方杂草稻资源和4份栽培稻为材料,研究了中国北方杂草稻的光合速率、蒸腾速率、气孔导度等光合与水分生理特性及其相互关系.结果表明: 北方杂草稻资源的光合和水分生理特性存在较大差异,具有丰富的多样性.杂草稻的光合速率变化范围在12.47～28.67 μmol CO₂·m^-2·s^-1,瞬时水分利用效率的变化范围在1.39～3.40 mg·g^-1.光合参数中,胞间CO₂浓度的变异系数最小,气孔导度的变异系数最大.光合速率与蒸腾速率、气孔导度呈极显著的二次曲线关系,光合速率与胞间CO₂浓度呈显著的直线关系,瞬时水分利用效率与蒸腾速率、气孔导度呈极显著的二次曲线关系.可用杂草稻材料的优越性能对栽培稻进行品种改良.     

Mechanisms of plant defense against insect herbivores

Plants respond to herbivory through various morphological, biochemicals, and molecular mechanisms to counter/offset the effects of herbivore attack. The biochemical mechanisms of defense against the herbivores are wide-ranging, highly dynamic, and are mediated both by direct and indirect defenses. The defensive compounds are either produced constitutively or in response to plant damage, and affect feeding, growth, and survival of herbivores. In addition, plants also release volatile organic compounds that attract the natural enemies of the herbivores. These strategies either act independently or in conjunction with each other. However, our understanding of these defensive mechanisms is still limited. Induced resistance could be exploited as an important tool for the pest management to minimize the amounts of insecticides used for pest control. Host plant resistance to insects, particularly, induced resistance, can also be manipulated with the use of chemical elicitors of secondary metabolites, which confer resistance to insects. By understanding the mechanisms of induced resistance, we can predict the herbivores that are likely to be affected by induced responses. The elicitors of induced responses can be sprayed on crop plants to build up the natural defense system against damage caused by herbivores. The induced responses can also be engineered genetically, so that the defensive compounds are constitutively produced in plants against are challenged by the herbivory. Induced resistance can be exploited for developing crop cultivars, which readily produce the inducible response upon mild infestation, and can act as one of components of integrated pest management for sustainable crop production.     

不同时期毛乌素沙区主要植物种光合作用和蒸腾作用的变化

 采用LI—6000便携式光合分析系统对毛乌素沙区主要植物种油蒿、中间锦鸡儿、旱柳进行了不同时期光合作用,蒸腾作用日进程的测定,并同步测定有效光辐射、空气相对湿度、叶温、气温、胞间CO2浓度、气孔阻力、叶片水势及土壤水势等因子;结果表明：不同时期、不同植物种其光合、蒸腾特征各异;植物的光合、蒸腾与环境因子和植物内部因子之间有密切关系,其中有效光辐射是影响光合作用、蒸腾作用诸因子中的主导因子,而气孔阻力变化则在调节光合和蒸腾中起着重要作用;不同植物种间气孔对环境条件变化的响应程度不同,以中间锦鸡儿最为灵敏;3种植物的水分利用效率表明,中间锦鸡儿的水分利用效率较油蒿、旱柳为高。     

拟单性木兰不同季节断根和剪枝后蒸腾和光合特性的变化

在2005年春季、夏季和秋季,对10a生拟单性木兰(Parakmeriaomeiensis)进行断根和剪枝处理,模拟移栽,用LICOR-6400测定了植株叶片的蒸腾速率、光合速率等生理指标,探讨这些生理指标对不同季节移栽成活率的影响。结果表明,春季处理后叶片能迅速关闭部分气孔,蒸腾速率和光合速率都减小,两者最低时约为对照的60%,生理机能的减弱有利于维持地上、地下部分的平衡,因而最有利于植株成活。夏季处理后叶片气孔导度显著增加,光合速率和蒸腾速率也随之增大,最高时约为对照的2倍左右,此时,若主要依靠剪枝来降低水分消耗,很难保证水分代谢平衡,移栽成活率低。秋季处理后植株叶片气孔导度高于对照,光合速率和蒸腾速率也增加,但增加幅度相对夏季较小,前期最高约增加40%,此时移栽可以通过适当的剪枝和增加土壤水分含量等措施提高成活率。可见,与水分相关的生理机能的调节机制,决定了移栽后的成活水平,即处理后能迅速调节自身生理机能、减少水分消耗的植株,成活率就高,反之就低。     

Interactions between plants and herbivores: A review of plant defense

Ecologists have long ignored or underestimated the importance of plant–herbivore interactions owing to the diversities of herbivores, plant defensive strategies and ecological systems. In this review, we briefly discussed the categories of herbivores. Then we reviewed the major types of plant defenses against herbivores. Selective forces of herbivore pressures have led to the evolution of various defensive mechanisms in plants, which can be classified into (i) resistance traits that reduce the amount of damage received, including physical, chemical, and biotic traits; (ii) tolerance mechanisms that decrease the impact of herbivore damage, and (iii) escape strategies that reduce the probability of plants to be found by herbivores. These strategies have been studied at different levels from molecular genetics and genomics, to chemistry and physiology, to community and ecosystem ecology. We summarized the development of the methodology for studying plant defenses against herbivores. Particularly, 24 of those hypotheses and models, which are influential in the international community concerning the relationship between plants and herbivores, including the defensive mimicry hypothesis, the compensatory continuum hypothesis, the slow-growth-high-mortality hypothesis, etc, were introduced and grouped into four categories according to plant defense strategies in the present review. Finally, we also reviewed the research progress of plant–herbivore interactions in China, and discussed the perspectives of studies on plant–herbivore interactions.     

Consequences of sequential attack for resistance to herbivores when plants have specific induced responses

Plants in nature are attacked sequentially by herbivores, and theory predicts that herbivore-specific responses allow plants to tailor their defenses. We present a novel field test of this hypothesis, and find that specific responses of Solanum dulcamara lead to season-long consequences for two naturally colonizing herbivores, irrespective of the second herbivore to attack plants. This result indicates that responses induced by the initial herbivore made plants less responsive to subsequent attack. We show that initial herbivory by flea beetles and tortoise beetles induce distinct plant chemical responses. Initial herbivory by flea beetles lowered the occurrence of conspecifics and tortoise beetles relative to controls. Conversely, initial herbivory by tortoise beetles did not influence future herbivory. Remarkably, the experimentally imposed second herbivore to feed on plants did not modify consequences (induced resistance or lack thereof) of the first attacker. Induction of plant chemical responses was consistent with these ecological effects; i.e. the second herbivore did not modify the plant's initial induced response. Thus, canalization of the plant resistance phenotype may constrain defensive responses in a rapidly changing environment.