沙柳光合作用和蒸腾作用日动态变化的初步研究

沙柳是毛乌素沙地流动沙丘和固定沙丘上广泛分布的重要固沙植物。叶片的光合速率呈现出不规则的日动态变化 ,在 1 0 :0 0～ 1 1 :0 0及 1 4 :0 0出现光合午休现象。蒸腾速率呈现出单峰型的日动态变化 ,蒸腾在午后 1 5:0 0达到最大。水分利用效率在早晨 9:0 0后保持在 2～ 2 .5μmol CO2 · mmol-1 H2 O左右。叶片水分亏缺也表现出规律性的变化。从早晨开始 ,叶片水分亏缺逐渐增大 ,在 1 8:0 0达到最大值。比较生长季节的不同时期环境因子的变化情况表明 ,春末的光照强度和气温比夏末高 ,但土壤水分含量则相反。沙柳在春末的光合速率、蒸腾速率分别是夏末的 79%和 72 .4% ,表明水分亏缺是影响沙柳生长发育的主要限制因素。沙柳在不同季节对水分的不同利用特点是对环境胁迫的弹性适应     

三种相思(Acacia)的光合作用与蒸腾作用的研究

本文主要探讨了三种相思的光合作用与蒸腾作用,并观测了不同时间内叶面气孔开启状况。 研究结果表明:三种相思中绢毛相思(A.holosericea)光合速率较高,在生长旺季高峰值可达23.16毫克CO_2·分米~(-2)·时~(-1)。此值较马占相思(A.marjian)高90％;较大叶相思(A.auriculaeformis)高22％。绢毛相思叶子生长速度较抉,叶绿素含量、比叶重也较高。在炎热的夏季,绢毛相思依靠叶片上的绒毛避免太阳光垂直照射,保持气孔开放,使光合作用保持正常。这是对环境的积极适应类型。面大叶相思则是利用增厚叶片角质层和关闭气孔的办法避免大量失水,致使光合作用速率下降。这是对环境的消极忍耐类型,这种类型可更加有效地利用水分。     

树种蒸腾作用、光合作用和蒸腾效率的比较研究

 各树种在年生长季不同测期的蒸腾速率日进程曲线一般呈单峰型。蒸腾速率与环境因子的相关性大小依次为：光照强度、气温、相对湿度和大气水势。蒸腾速率日变化一般可用具有光照因子的优化模型(即光照型、光温型、光湿型和光温湿型)来模拟。年生长季树种蒸腾速率(g·g-1LD·h-1)排序由大到小为：柠条(0.9269±0.2089)(平均值±标准差,以下同)、小叶杨(0.7177±0.2410)、河北杨(0.6256±0.1609)和北京杨(0.6007±0.2749);净光合速率(mgCO2·g-1LD·h-1)排序自高至低为：柠条(14.5949±4.6627)、小叶杨(13.4055±2.9994)、河北杨(13.2569±4.3531)和北京杨(11.6989±2.5884);蒸腾效率(gDM·g-1H2O)排序由高至低为：北京杨(1.41％±0.42％)、河北杨(1.35％±0.36％)、小叶杨(1.26％±0.23％)和柠条(1.00％±0.27％)。     

铜毒对海州香薷(Elsholtzia splendens)不同种群光合作用和蒸腾作用的影响

通过水培实验,对种子分别来自湖北省铜绿山、赤马山铜矿区和红安非矿区的海州香薷种群在铜胁迫下的光合作用和蒸腾作用进行了比较研究。结果发现,矿区两个种群在铜胁迫下的光合能力明显比非矿区种群强,尤其在高Cu（100μmol／M）处理更为显著：如铜绿山和赤马山叶片净光合速率分别为13．15μmol CO2m^-2s^-1和12．59μmol CO2m^-2s^-1,为红安种群（1．07μmol CO2m^-2s^-1）的13倍;铜绿山和赤马山种群的光能利用效率分别为0．0221μmol CO2μmol^-1和0．0224μmol CO2μmol^-1photon,为红安种群（0．0031μmol CO2μmol^-1photon）的7倍。表观量子产额在两个矿区种群中没有明显的变化,低Cu（5和20μmol／L）处理促进了矿区种群叶绿素（Chl a和Chl b）含量的增加,而非矿区种群的这两个指标则随处理浓度的增加而迅速下降。来自矿区两个种群的蒸腾速率受铜的胁迫影响较小,而来自非矿区种群随处理浓度的加大而明显降低,其叶片的蒸腾速率在5、20μmol／L和100μmol／L浓度处理时迅速下降为对照的62．74％、50．96％和42．6％;水分利用效率在矿区两个种群中随处理水平的增大而提高,在100μmol／L处理时铜绿山和赤马山种群分别是对照的161．83％和130．41％,而非矿区种群随处理浓度的增加而急剧降低。另外,矿区两个种群的呼吸速率和气孔阻力随处理浓度的降低和升高的幅度明显比非矿区小。总之,在铜污染胁迫下,矿区种群保持的这种生理生态特性是其能在这种环境中正常生长定居的重要原因,是其长期进化的结果。     

铜毒对海州香薷（Elsholtzia splendens）不同种群光合作用和蒸腾作用的影响

通过水培实验,对种子分别来自湖北省铜绿山、赤马山铜矿区和红安非矿区的海州香薷种群在铜胁迫下的光合作用和蒸腾作用进行了比较研究。结果发现, 矿区两个种群在铜胁迫下的光合能力明显比非矿区种群强,尤其在高Cu(100μmol/M)处理更为显著：如铜绿山和赤马山叶片净光合速率分别为13.15μmol CO₂ m^-2 s^-1和12.59μmolCO₂ m^-2 s^-1,为红安种群(1.07μmol CO₂ m^-2 s^-1)的13倍;铜绿山和赤马山种群的光能利用效率分别为0.0221μmol CO₂ μmol^-1和0.0224μmol CO₂ μmol^-1 photon,为红安种群(0.003μmolCO₂ μmol^-1 photon)的7倍。表观量子产额在两个矿区种群中没有明显的变化,低Cu (5和20μmol/L)处理促进了矿区种群叶绿素（Chl a 和Chl b）含量的增加,而非矿区种群的这两个指标则随处理浓度的增加而迅速下降。来自矿区两个种群的蒸腾速率受铜的胁迫影响较小,而来自非矿区种群随处理浓度的加大而明显降低,其叶片的蒸腾速率在5、20μmol/L和100μmol/L浓度处理时迅速下降为对照的62.74%、50.96%和42.6%;水分利用效率在矿区两个种群中随处理水平的增大而提高,在100μmol/L处理时铜绿山和赤马山种群分别是对照的161.83%和130.41%,而非矿区种群随处理浓度的增加而急剧降低。另外,矿区两个种群的呼吸速率和气孔阻力随处理浓度的降低和升高的幅度明显比非矿区小。总之,在铜污染胁迫下,矿区种群保持的这种生理生态特性是其能在这种环境中正常生长定居的重要原因,是其长期进化的结果。     

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。     

芦苇（Phragmites communis）光合作用与蒸腾作用的日进程

测定了野生芦苇（Ｐｈｒａｇｍｉｔｅｓｃｏｍｍｕｎｉｓ）光合作用、蒸腾作用及相关指标的日变化。叶片的净光合作用率在１０∶００～１５∶００间保持一个高的稳定阶段,平均为７３～９９μｍｏｌＣＯ２·ｍ－２·ｓ－１,光饱和状态下的最大值为１２７μｍｏｌＣＯ２·ｍ－２·ｓ－１,处于挺水植物的低限。蒸腾作用强度的峰值达４８ｍｍｏｌＨ２Ｏ·ｍ－２·ｓ－１。光合作用和蒸腾作用的日进程均未发生“午休”现象;相反,二者都是在正午前后强度最大。光合光量子流密度与净光合作用率、蒸腾强度、叶面传导率均存在不同程度的正相关。芦苇的光合作用强度和水分利用效率相对较低,但年生产量却较高,这是因为芦苇具有密实的叶子、有利的叶片配置结构和高的蒸腾作用强度。     

气温升高与干旱胁迫对宁夏枸杞光合作用的影响

以宁夏枸杞1年生苗木为材料,采用开顶式生长室模拟增温环境,设置两个温度水平(正常环境温度,增温=正常环境温度+2.5—3.7℃)和3个土壤水分水平(正常水分条件(田间最大持水量的70%—75%)、中度干旱处理(田间最大持水量的50%—55%)和重度干旱处理(田间最大持水量的35%—40%)),研究气温升高和干旱胁迫对宁夏枸杞光合作用的影响。结果表明:(1)在增温条件下,中度和重度干旱处理下的净光合速率比对照(正常供水)分别下降17.5%、48.9%,气孔导度平均下降了3.9%,水分利用效率仅为正常环境温度下的57.8%。(2)在气温升高和干旱胁迫交互作用下,枸杞叶片的净光合速率、气孔导度、胞间CO2浓度显著下降的同时,增温处理又加剧了枸杞植株的蒸腾耗水,从而导致枸杞叶片水分的利用效率和CO2同化能力降低。(3)气温升高和干旱胁迫交互作用降低了枸杞的PSⅡ活性中心的光能转换效率、使光合机构和PSⅡ反应中心受到损伤,从而导致枸杞光合作用效率下降。(4)气温升高加剧了干旱胁迫对宁夏枸杞叶片净光合速率和水分利用效率的减小作用,即气温升高加剧了干旱胁迫对宁夏枸杞光合作用的抑制作用。     

光合作用—蒸腾作用—气孔导度的耦合模型及C3植物叶片对环境因子的生理 …

以叶片的气体传输过程为基础,将蒸腾作用包括在以往光合作用－气孔导度的耦合模型中,建立了光合作用－蒸腾作用－气孔导度的耦合模型。该模型可以模拟边界层导度对生理过程的影响。模拟了Ｃ３植物叶片对环境因子,如光照、温度、湿度、边界层导度和ＣＯ２浓度等的生理响应（光合作用、蒸腾作用、气孔导度）以及Ｃｉ和水分利用效率的变化。在环境因子变化于较大范围的情况下,模拟结果符合许多实验结论。     

光合作用-蒸腾作用-气孔导度的耦合模型及C_3植物叶片对环境因子的生理响应(英文)

以叶片的气体传输过程为基础,将蒸腾作用包括在以往光合作用气孔导度的耦合模型中,建立了光合作用蒸腾作用气孔导度的耦合模型。该模型可以模拟边界层导度对生理过程的影响。模拟了Ｃ３植物叶片对环境因子,如光照、温度、湿度、边界层导度和ＣＯ２浓度等的生理响应（光合作用、蒸腾作用、气孔导度）以及Ｃｉ和水分利用效率的变化。在环境因子变化于较大范围的情况下,模拟结果符合许多实验结论。     

土壤干旱条件下不同施钾水平对烟草光合速率和蒸腾效率的影响

研究了土壤干旱条件下,不同的施钾水平对烟草光合速率,胞间CO2浓度,气孔导度,蒸腾速率,蒸腾效率及生物量的影响。结果表明：在土壤干旱条件下适量施钾可以减少叶肉细胞光合活性的下降,消弱非气孔因素对光合的限制,增强气孔调节能力,提高蒸腾效率,并获得较高的生物量。     

Requirements for obtaining maximum indices of photosynthesis and transpiration in attached leaves of willow plants grown in short-rotation forest

The results of multiyear studies of gas exchange in intact attached leaves of several willow species (Salix sp.) were analyzed. Measurements were performed with a portable Li-6400 infrared gas analyzer both on plants in their natural environment and on rooted cuttings grown in a greenhouse. Individual attached leaves were placed into the leaf chamber where climatic conditions were either similar to or different from those outside the chamber. The maximal rates of net photosynthesis (P _n) and transpiration (E) were only observed with the provision that the environmental variables inside and outside the chamber were identical. On rainy or cloudy days, the P _n and E values observed under optimum conditions inside the leaf chamber were lower than their potential maxima by 12–18% and 35–45%, respectively. Deviation of temperature in the chamber by 5–7°C from the external level and fluctuations of ambient temperature affected P _n but not E rates of tested leaves. Variations in relative air humidity in the chamber directly influenced E but had no effect on P _n of attached leaves. It was shown that the maximum rates of gas exchange in the attached willow leaf could be only attained by providing optimum conditions for the whole plant.     

滇北球花报春和滇海水仙花的光合特性研究

用LI-6400便携式光合测定仪对引种栽培的滇北球花报春和滇海水仙花的光合参数进行测定,以探讨其光合生理特性.结果表明:(1)滇北球花报春的净光合速率(P_n)和蒸腾速率(T_r)日进程曲线均呈单峰型,它们的峰值分别出现在13:00和16:00;滇海水仙花的P_n、Tr较滇北球花报春低,且在一定范围内保持稳定,没有明显的峰值,与滇北球花报春表现出较明显的种间差异;(2)两种报春比叶重( LMA)和叶氮含量(LNC_a)对其光合相关特征参数没有显著影响,而叶氮在Rubisco中的分配系数PR、生物能库中的分配系数P_B和光合组分中总氮含量N_P与光合特征参数LCP、V_(cmax)、J_(max)、CE具有显著的正相关关系;(3)滇北球花报春具有较高的气孔导度(G_s)、P_n和T_r,对强光、高温、低湿度表现出较强的环境适应性,表现出较强的光合能力.     

亚高温下不同空气湿度对番茄光合作用和物质积累的影响

为了研究亚高温下不同空气湿度对番茄植株光合作用及物质积累的影响,本试验利用人工气候室,在11:00—15:00平均温度为33℃的亚高温条件下,设置3个空气相对湿度处理,分别为70%～80%(高湿)、50%～60%(中湿)和不加湿的30%～40%(低湿)。结果表明:在处理25d时,高湿处理番茄叶片叶绿素含量、净光合速率显著高于低湿处理,而低湿处理果实空洞率比高湿处理高18.4%(P<0.05);在33℃亚高温条件下,70%～80%的相对湿度有利于光合作用的增强和果实品质的提高。     

A coupled model of stomatal conductance, photosynthesis and transpiration

A model that couples stomatal conductance, photosynthesis, leaf energy balance and transport of water through the soil–plant–atmosphere continuum is presented. Stomatal conductance in the model depends on light, temperature and intercellular CO₂ concentration via photosynthesis and on leaf water potential, which in turn is a function of soil water potential, the rate of water flow through the soil and plant, and on xylem hydraulic resistance. Water transport from soil to roots is simulated through solution of Richards’ equation. The model captures the observed hysteresis in diurnal variations in stomatal conductance, assimilation rate and transpiration for plant canopies. Hysteresis arises because atmospheric demand for water from the leaves typically peaks in mid‐afternoon and because of uneven distribution of soil matric potentials with distance from the roots. Potentials at the root surfaces are lower than in the bulk soil, and once soil water supply starts to limit transpiration, root potentials are substantially less negative in the morning than in the afternoon. This leads to higher stomatal conductances, CO₂ assimilation and transpiration in the morning compared to later in the day. Stomatal conductance is sensitive to soil and plant hydraulic properties and to root length density only after approximately 10 d of soil drying, when supply of water by the soil to the roots becomes limiting. High atmospheric demand causes transpiration rates, LE, to decline at a slightly higher soil water content, θ_s, than at low atmospheric demand, but all curves of LE versus θ_s fall on the same line when soil water supply limits transpiration. Stomatal conductance cannot be modelled in isolation, but must be fully coupled with models of photosynthesis/respiration and the transport of water from soil, through roots, stems and leaves to the atmosphere.     

Direct and indirect climate change effects on photosynthesis and transpiration

Climate change affects plants in many different ways. Increasing CO(2) concentration can increase photosynthetic rates. This is especially pronounced for C(3) plants, at high temperatures and under water-limited conditions. Increasing temperature also affects photosynthesis, but plants have a considerable ability to adapt to their growth conditions and can function even at extremely high temperatures, provided adequate water is available. Temperature optima differ between species and growth conditions, and are higher in elevated atmospheric CO(2). With increasing temperature, vapour pressure deficits of the air may increase, with a concomitant increase in the transpiration rate from plant canopies. However, if stomata close in response to increasing CO(2) concentration, or if there is a reduction in the diurnal temperature range, then transpiration rates may even decrease. Soil organic matter decomposition rates are likely to be stimulated by higher temperatures, so that nutrients can be more readily mineralised and made available to plants. This is likely to increase photosynthetic carbon gain in nutrient-limited systems. All the factors listed above interact strongly so that, for different combinations of increases in temperature and CO(2) concentration, and for systems in different climatic regions and primarily affected by water or nutrient limitations, photosynthesis must be expected to respond differently to the same climatic changes.     

The effect of vapor pressure deficit on maize transpiration response to a drying soil

A decline in plant transpiration has been widely observed to occur within a fairly stable range of threshold values of fraction transpirable soil water (FTSW), usually 0.3–0.4. However, the stability of this function has not been compared at various levels of atmospheric vapor pressure deficit (VPD). Soil hydraulic conductivity is likely to be involved in determining the threshold where water supply is limiting. Thus, it was hypothesized that at a high VPD resulting in increased transpiration rates, the FTSW threshold for the decline of transpiration rates as a result of drying soil would be increased. This study was undertaken in controlled environment chambers with two maize (Zea mays L.) hybrids (Pioneer Brand Hybrids `3165' and `3737') so as to subject plants to four VPD levels (1.1, 2.0, 2.9 and 3.6 kPa) during a soil drying experiment. In contrast to the original hypothesis, there was little ( 0.05 FTSW) change in the threshold FTSW in response to increased VPD for either hybrid. In fact, over the narrow 0.31–0.38 FTSW range observed, the two hybrids showed opposite trends in FTSW threshold as VPD increased. These results supported the view that the FTSW threshold for the decline in transpiration with drying soil is stable, showing little sensitivity to changes in VPD.     

铝胁迫对蓼科植物生长和光合、蒸腾特性的影响

采用水培试验,设置5种铝处理浓度,研究了铝对3种蓼科植物酸模叶蓼、杠板归和辣蓼叶片光合、蒸腾和叶绿素荧光参数的影响。结果表明,高铝处理(400μmol.L-1)显著抑制3种蓼科植物地上部和根系生长,并且导致3种蓼科植物叶片叶绿素含量、Chla/Chlb、净光合速率(Pn)、水分利用效率(WUE)、PSII光合电子传递量子效率(φPSII)和光化学猝灭系数(qP)显著下降。中低铝处理(25~100μmol.L-1)时,与对照相比,酸模叶蓼生物量显著增加,杠板归显著减少,辣蓼先增加后减少。其中,酸模叶蓼和辣蓼叶绿素含量、Chla/Chlb、Pn、蒸腾速率(Tr)、胞间CO2浓度(Ci)、PSII最大光化学效率(Fv/Fm)、qP均未发生显著变化,但辣蓼WUE、φPSII和非光化学猝灭系数(NPQ)显著下降,酸模叶蓼无显著变化;而杠板归除Ci、Fv/Fm外,其余叶片光合、蒸腾及叶绿素荧光参数均出现显著下降。上述结果表明,酸模叶蓼在中低铝处理条件下可通过保持较高的叶绿素含量、Chla/Chlb、WUE、Pn、PSII反应中心光化学反应效率以及提高非辐射能量耗散来增强其对铝的耐性。     

环境因子对辣椒光合与蒸腾特性的影响

采用灰色关联分析方法研究环境因子对辣椒(Capsicum annuum Linn.)光合和蒸腾特性的影响.结果表明,在强光照下影响净光合速率的环境因子大小顺序为相对湿度、CO2浓度、温度、光照强度、气孔导度;净光合速率与相对湿度、叶温呈显著的负相关,与CO2浓度呈极显著的正相关;蒸腾速率与气温呈极显著的正相关,与相对湿度呈极显著的负相关;水分利用效率与相对湿度呈极显著的正相关,与温度呈极显著的负相关.弱光照时影响净光合速率的环境因子大小顺序为光照强度、温度、相对湿度、CO2浓度;净光合速率与光照强度、CO2浓度呈显著的正相关,与相对湿度呈显著的负相关.在强光照下适当遮阳、灌水、增施CO2肥,在弱光照下减少荫蔽、通风透气、降低相对湿度、增加温度可促进辣椒光合作用,提高辣椒产量.