Effects of leaf shape plasticity on leaf surface temperature

干旱区植物叶片形态可塑性是植物适应高温干旱环境的重要生存策略, 但目前仍缺乏直观的数据予以证明。该研究应用热成像技术和图像分析技术, 同步测定真实叶片与模拟叶片的叶温、形态及风速、辐射和温度等环境参数。研究结果显示: 在干旱、高温环境下, 除了蒸腾, 叶片形态变化也是调控叶温的重要因子。干旱区植物叶片变小, 有利于加速叶片与环境的物质及热量交换, 从而达到降低叶温的目的。样地数据显示, 在高温、低风速环境下, 叶片宽度每减少1 cm, 叶片表面温度降低约2.1 ℃, 而模拟叶片叶宽度每减少1 cm, 叶片表面温度降低0.60-0.86 ℃。该研究对深入理解植物生存策略与环境适能力具有重要意义。     

干旱区植物叶片大小对叶表面蒸腾及叶温的影响

利用热及物质交换原理, 并结合前人研究成果, 在单叶尺度上建立了简单的叶温和水气蒸腾模型。模型通过预设值驱动, 预设值参照干旱区环境及植物叶片特征设置。模拟结果显示: 随气孔阻力的增加, 叶片蒸腾速率降低, 叶温升高; 同一环境下, 具有低辐射吸收率的叶片蒸腾速率和叶温更低, 并且气孔阻力越大, 这种差异越明显。另外, 叶片宽度及风速是影响叶片蒸腾及叶温的重要因子。干旱地区植物生长季节, 风速小于0.1 m·s ^-1、气孔阻力接近1000 s·m ^-1时, 降低叶片宽度不仅有利于降低叶片温度, 而且能够降低叶片蒸腾速率, 从而实现保持水分, 增强植物适应高温、干旱的能力。     

形态变化对叶片表面温度的影响

干旱区植物叶片形态可塑性是植物适应高温干旱环境的重要生存策略, 但目前仍缺乏直观的数据予以证明。该研究应用热成像技术和图像分析技术, 同步测定真实叶片与模拟叶片的叶温、形态及风速、辐射和温度等环境参数。研究结果显示: 在干旱、高温环境下, 除了蒸腾, 叶片形态变化也是调控叶温的重要因子。干旱区植物叶片变小, 有利于加速叶片与环境的物质及热量交换, 从而达到降低叶温的目的。样地数据显示, 在高温、低风速环境下, 叶片宽度每减少1 cm, 叶片表面温度降低约2.1 ℃, 而模拟叶片叶宽度每减少1 cm, 叶片表面温度降低0.60-0.86 ℃。该研究对深入理解植物生存策略与环境适能力具有重要意义。     

Relationships between sclerophylly,leaf biomechanical properties and leaf anatomy in some Australian heath and forest species

ABSTRACT

A previous study of 19 south-east Australian heath and forest species with a range of leaf textures showed that they varied considerably in leaf biomechanical properties. By using an index of sclerophylly derived from botanists' rankings (botanists' sclerophylly index, BSI) we determined that leaves considered by botanists to be sclerophyllous generally had both high strength and work to fracture (particularly in punching and tearing tests), both at the level of leaf and per unit leaf thickness. In the current study we have shown that leaves from the same species also varied considerably in leaf specific mass (46–251 g m^-2), neutral detergent fibre concentration (20–59% on a dry weight basis) and in leaf anatomy. Multiple regression indicated a very strong correlation between BSI and the first two components of a principal components analysis (PCA) of leaf anatomy (R ² = 0.91). In addition, there was strong correlation between the first component of a PCA of the mechanical properties (correlated with BSI) and the two axes derived from anatomical characteristics (R ² = 0.66). The anatomical properties contributing most to the significant component axes were thickness of palisade mesophyll and upper cuticle (axis 1) and percentage fibre (neutral detergent fibre) and lower epidermis thickness (axis 2). However, whether these relationships are causal, or reflect correlations with characteristics not measured in this study, such as vascularization and sclerification, is not clear. At a finer scale, however, there is evidence that there are various ways to be sclerophyllous, both in terms of anatomical and mechanical properties. This is illustrated by comparison of two of the sclerophyllous species, Eucalyptus baxteri and Banksia marginata.     

Evolution of leaf developmental mechanisms

Leaves are determinate organs produced by the shoot apical meristem. Land plants demonstrate a large range of variation in leaf form. Here we discuss evolution of leaf form in the context of our current understanding of leaf development, as this has emerged from molecular genetic studies in model organisms. We also discuss specific examples where parallel studies of development in different species have helped understanding how diversification of leaf form may occur in nature.     

Variations in the relationship between maximum leaf carboxylation rate and leaf nitrogen concentration

叶片最大羧化速率是表征植物光合能力的关键参数, 受到光照、温度、水分、CO₂浓度、叶片氮含量等多个要素的控制。准确地模拟植物叶片最大羧化速率对环境因子的响应是预测未来植被生产力和碳循环过程的前提。目前大多数陆地碳循环过程模型以Farqhuar光合作用模型为基础模拟植物的光合作用, 关于植物叶片的最大羧化速率与叶氮含量关系的模拟方法却各不相同。该文汇总了1990-2013年国内外植物叶片光合速率观测研究文献中叶片最大羧化速率与叶氮含量的关系式及相关数据, 分析了叶片最大羧化速率与叶氮含量关系随不同植被功能型和时间的变化特征, 以及环境因子变化条件下最大羧化速率与叶氮含量关系的变化特征, 探讨了二者关系变异性的可能原因以及影响因子。结果表明: 1)不同功能型植物叶片的最大羧化速率和叶氮含量的关系存在较大差异, 二者线性关系式的斜率平均值变化范围为16.29-50.25 μmol CO₂·g N^-1·s^-1。落叶植被叶片的最大羧化速率随叶氮含量的变化率和光合氮利用效率一般都高于常绿植被, 其变异主要源于植物的比叶重和叶片内部氮素分配的差异。2)叶片最大羧化速率随叶氮含量的变化存在季节和年际变异。在没有受到水分胁迫的年份中, 叶片最大羧化速率随叶氮含量变化的速率一般在春季或夏季最高, 其季节变异与比叶重和叶氮在Rubisco的分配比例的季节变化有关。受到干旱的影响, 叶片最大羧化速率随叶氮含量的变化率会升高。3)当大气CO₂浓度增加时, 由于叶片中Rubisco含量的降低, 多年生针叶叶片最大羧化速率和叶氮关系斜率值会出现降低; 当供氮水平增加时, 叶片最大羧化速率和叶片氮含量均表现出增加趋势, 二者线性关系的斜率也相应增加。在此基础上, 该文指出在模拟叶片最大羧化速率与叶氮含量的关系时, 应考虑叶片比叶重和叶氮在Rubisco中的分配比例的季节变异、水分胁迫、大气CO₂浓度和供氮水平变化对二者关系的影响。囿于数据的有限性, 今后应进一步加强多因子控制实验研究, 深入探讨叶片最大羧化速率与叶氮含量关系的变异性机理, 并获得更系统的观测数据, 以助生态系统过程模型的改进, 提高模型的模拟精度。     

Decline of photosynthetic capacity with leaf age in relation to leaf longevities for five tropical canopy tree species

The effect of leaf aging on photosynthetic capacities was examined for upper canopy leaves of five tropical tree species in a seasonally dry forest in Panama. These species varied in mean leaf longevity between 174 and 315 d, and in maximum leaf life span between 304 and 679 d. The light-saturated CO2 exchange rates of leaves produced during the primary annual leaf flush measured at 7-8 mo of age were 33-65% of the rates measured at 1-2 mo of age for species with leaf life span of < 1 yr. The negative regression slopes of photosynthetic capacity against leaf age were steeper for species with shorter maximum leaf longevity. In all species, regression slopes were less steep than the slopes predicted by assuming a linear decline toward the maximum leaf age (20-80% of the predicted decline rate). Maximum oxygen evolution rates and leaf nitrogen content declined faster with age for species with shorter leaf life spans. Statistical significance of regression slopes of oxygen evolution rates against leaf age was strongest on a leaf mass basis (r = 0.49-0.87), followed by leaf nitrogen basis (r = 0.48-0.77), and weakest on a leaf area basis (r = 0.35-0.70).     

植物叶片最大羧化速率与叶氮含量关系的变异性

叶片最大羧化速率是表征植物光合能力的关键参数, 受到光照、温度、水分、CO₂浓度、叶片氮含量等多个要素的控制。准确地模拟植物叶片最大羧化速率对环境因子的响应是预测未来植被生产力和碳循环过程的前提。目前大多数陆地碳循环过程模型以Farqhuar光合作用模型为基础模拟植物的光合作用, 关于植物叶片的最大羧化速率与叶氮含量关系的模拟方法却各不相同。该文汇总了1990-2013年国内外植物叶片光合速率观测研究文献中叶片最大羧化速率与叶氮含量的关系式及相关数据, 分析了叶片最大羧化速率与叶氮含量关系随不同植被功能型和时间的变化特征, 以及环境因子变化条件下最大羧化速率与叶氮含量关系的变化特征, 探讨了二者关系变异性的可能原因以及影响因子。结果表明: 1)不同功能型植物叶片的最大羧化速率和叶氮含量的关系存在较大差异, 二者线性关系式的斜率平均值变化范围为16.29-50.25 μmol CO₂·g N^-1·s^-1。落叶植被叶片的最大羧化速率随叶氮含量的变化率和光合氮利用效率一般都高于常绿植被, 其变异主要源于植物的比叶重和叶片内部氮素分配的差异。2)叶片最大羧化速率随叶氮含量的变化存在季节和年际变异。在没有受到水分胁迫的年份中, 叶片最大羧化速率随叶氮含量变化的速率一般在春季或夏季最高, 其季节变异与比叶重和叶氮在Rubisco的分配比例的季节变化有关。受到干旱的影响, 叶片最大羧化速率随叶氮含量的变化率会升高。3)当大气CO₂浓度增加时, 由于叶片中Rubisco含量的降低, 多年生针叶叶片最大羧化速率和叶氮关系斜率值会出现降低; 当供氮水平增加时, 叶片最大羧化速率和叶片氮含量均表现出增加趋势, 二者线性关系的斜率也相应增加。在此基础上, 该文指出在模拟叶片最大羧化速率与叶氮含量的关系时, 应考虑叶片比叶重和叶氮在Rubisco中的分配比例的季节变异、水分胁迫、大气CO₂浓度和供氮水平变化对二者关系的影响。囿于数据的有限性, 今后应进一步加强多因子控制实验研究, 深入探讨叶片最大羧化速率与叶氮含量关系的变异性机理, 并获得更系统的观测数据, 以助生态系统过程模型的改进, 提高模型的模拟精度。     

Determinants of some leaf characteristics of Australian mangroves

Leaf characteristics reflecting the size, lifespan (longevity), moisture content (degree of succulence) and complexity of structure of 20 mangrove species were studied over several years at 13 locations along the tropical and subtropical Australian coast. These characteristics were found to fall generally within the ranges of those for woody species from other ecosystems. With the exception of one species, it was found that leaf longevity was related inversely to leaf moisture content, increasing from nearly 6 months in more succulent species to over 2 years in less succulent species. This suggested that more succulent leaves are less complex in their structure because they have less well‐developed ability to compartmentalize salt. There was a tendency also for leaf longevity to increase in species with larger leaves. These findings were consistent with the general view for land plants that leaf longevity is greater in species that have developed tolerance to environmental stress, salt particularly in the case of mangroves. Leaf tissue in such species is more robust or complex and requires greater metabolic resources in its construction; the plant is then advantaged by retaining the tissue for longer periods. Classification of the species considered here, based on their leaf longevity, moisture content and complexity, identified phylogenetically related species groupings that reflected these leaf longevity effects.     

不同沙丘生境主要植物比叶面积和叶干物质含量的比较

研究了生长在不同沙丘生境中 (流动沙丘 ,半固定沙丘和固定沙丘 ) 2 0个植物种 (10个 1年生植物种和 10个多年生植物种 )的比叶面积 (SL A)和叶干物质含量 (L DMC)的变化 ,并且分析了各个沙丘生境的土壤养分特征。结果表明 ,各个植物种的平均 SL A和 L DMC在植物种之间差异显著 ;多数在两种或 3种沙丘生境均有分布的植物其 SL A在不同沙丘生境之间差异显著 ,但是仅有 6个植物种的 L DMC在不同沙丘生境之间表现出差异 (p<0 .0 5 )。与许多研究结果类似 ,1年生植物的 SL A显著大于多年生植物的 SL A,而且两者之间 L DMC存在一定的差异。 1年生植物 SL A和 L DMC之间相关性不显著 ,但多年生植物SL A和 L DMC之间呈显著负相关。综合所有 2 0个植物种可以发现 ,SL A增大时 ,L DMC有下降的趋势     

茶树种质叶片色素含量与叶色参数的关系

为了探究茶树种质资源叶片色素含量与叶色参数之间的关系,以143份黄、白化和紫化叶色特异茶树种质为材料,比较分析各种质叶片叶色参数L*、ɑ*、b*值和花青素、叶绿素、类胡萝卜素含量差异,并通过主成分分析、聚类分析、相关性分析、多元逐步回归分析和通径分析探讨叶片色素含量和叶色参数关系,为叶色特异茶树种质叶片呈色机理及品种选育提供依据。结果表明:(1)紫化茶树种质花青素含量和ɑ*值较高,叶片呈现紫红色;黄化种质类胡萝卜素含量/叶绿素含量比值和b*值较高,叶片呈黄色,白化种质L*值较高,叶片呈白色。在叶色表型性状方面,叶色特异茶树种质大体聚为两大类群,白色系和黄色系聚为一大类,紫色系聚为另一大类。(2)叶色特异茶树种质叶片叶色参数ɑ*值与花青素含量呈极显著正相关,L*值、b*值与花青素和叶绿素含量均呈极显著负相关,且b*值与类胡萝卜素含量呈极显著正相关;花青素、叶绿素对叶片CIEL*ɑ*b*值直接作用较大。总之,ɑ*值可作为描述叶色特异茶树种质叶片紫红色性状的代表性参数,b*值可作为描述叶色特异茶树种质叶片黄色性状的代表性参数。     

Changes in leaf optical properties associated with light-dependent chloroplast movements

We surveyed 24 plant species to examine how leaf anatomy influenced chloroplast movement and how the optical properties of leaves change with chloroplast position. All species examined exhibited light-dependent chloroplast movements but the associated changes in leaf absorptance varied considerably in magnitude. Chloroplast movement-dependent changes in leaf absorptance were greatest in shade species, in which absorptance changes of >10% were observed between high- and low-light treatments. Using the Kubelka-Munk theory, we found that changes in the absorption (k) and chlorophyll a absorption efficiency (k*) associated with chloroplast movement correlated with cell diameter, such that the narrower, more columnar cells found in sun leaves restricted the ability of chloroplasts to move. The broader, more spherical cells of shade leaves allowed greater chloroplast rearrangements and in low-light conditions allowed efficient light capture. Across the species tested, light-dependent chloroplast movements modulated leaf optical properties and light absorption efficiency by manipulating the package (sieve or flattening) effect but not the detour (path lengthening) effect.     

Diurnal cycles of leaf extension in unsalinized and salinized Beta vulgaris

Abstract. Continuous high resolution measurement of sugar beet leaf extension over 5 d in growth chambers showed average leaf extension rates (LER) in darkness to be from three to six times those in light for plants growing in non-salinized media. The changes in LER in light-dark transitions occurred within seconds, a response which was more rapid than stomatal opening or closing. When the growth medium was salinized to 100 mol m⁻³ NaCl, LER's were reduced by about 50% in darkness and 90% in light, markedly increasing the ratio of dark to light LER.
A 2-d episode of root-zone salinity imposed midway through a 5-d period of measurement decreased LER and produced higher leaf temperatures. LER and diurnal leaf temperature patterns reverted to their pre-salinized levels when root-zone salinity was removed. Thus, the effects of short episodes of high sodium chloride in the growth medium appear to be reversible, suggesting a water stress mechanism of growth reduction rather than toxicity effects of salt.     

观察植物叶迹、叶隙立体结构的实验方法

通过实验研究提出了观察植物叶迹、叶隙立体结构的方法。对观察节处维管组织的变化, 有重要意义。     

落叶收集法测定叶面积指数的快速取样方法

叶面积指数(LAI)是植被冠层结构的一个重要参数,它不仅是许多生态和气候模型的重要输入变量,而且是生态系统动态变化监测的一个重要指标。LAI可通过各种间接和直接的手段来观测,而间接观测的LAI值常常需要直接的观测数据来校验。落叶收集法是一种广泛使用的直接观测LAI的方法,过去的研究还未发现有涉及落叶收集的取样技术及其观测精度的内容。对长白山和北京地区落叶阔叶林的落叶进行了3a的观测,每年一次性收集落叶样品分析,研究结果表明:①不同层次落叶的含水量差异巨大,且落叶含水量的日变化明显。上下层落叶的含水量绝对值差异高达10%以上,日变化绝对值差异高达20%以上。因此,在野外收集落叶样本时,为减小落叶含水量变化所导致的LAI观测误差,应从上到下直到地面进行取样,且尽可能多地收集落叶样本。②在落叶阔叶人工林和天然林里,无论样地的大小(1hm2或30m×30m样地),无论取样单元的大小(1m2或25m2分辨率),林内的LAI分布很不均匀,LAI介于0-15.5(1m2分辨率的1hm2样地)或者2.6-9.1(25m2分辨率的30m×30m样地)。③要准确测定落叶林的LAI,收集落叶的样地面积越大越好,且尽量选择地势平坦的样地。对于1hm2或者30m×30m大小的样地,可随机布设一个10m×10m的小样地来观测,精度分别可达85%、80%。④10m×10m小样地的LAI观测,可将其分为4个相邻的5m×5m小样进行取样。对每个5m×5m小样,快速的取样方法是:Ⅰ.随机布设6个1m2取样,这样取样可以保证在99%概率水平上,100m2、30m×30m和1hm2样地的LAI观测精度分别为90%、75%、70%左右。Ⅱ.随机布设11个1m2取样。可以保证在99%概率水平上,100m2、30m×30m和1hm2样地的LAI观测精度分别为94%、80%、75%左右。