干旱胁迫下胡杨光合光响应过程模拟与模型比较

以塔里木干旱荒漠区2年生胡杨幼苗为试材,盆栽模拟荒漠生境5种水分梯度,利用Li-6400便携式光合作用系统测定胡杨在干旱胁迫下光合作用的光响应过程,并采用4种光响应模型对其进行拟合与比较,以期优选出适用于干旱荒漠环境的光响应模型,阐明胡杨光合作用对干旱胁迫的响应规律与适应机制。结果表明:胡杨净光合速率(P_n)随干旱胁迫加剧呈下降趋势,同一光强(PAR)下P_n降幅增大。中度干旱胁迫以下(土壤相对含水量,RSWC45%)胡杨在高PAR下仍能维持相对较高P_n,光抑制程度轻;直角双曲线、非直角双曲线和指数模型均可较好地模拟P_n-PAR响应过程,但最大净光合速率(P_(nmax))、光饱和点(LSP)拟合值与实测值差异极显著(P0.01)。中度干旱胁迫以上(RSWC45%)胡杨P_n随PAR升高而显著下降,LSP与P_(nmax)极显著降低,光抑制现象明显;仅直角双曲线修正模型拟合的胡杨光响应过程、光响应参数与实际情况较吻合。4种模型模拟效果顺序:直角双曲线修正模型指数模型非直角双曲线模型直角双曲线模型。4种光响应模型对干旱胁迫具有不同的适应性,直角双曲线修正模型适用于各种水分条件,尤其适用于干旱荒漠生境,其它3种模型适用于水分条件较好的生境。光响应特征参数对干旱胁迫的响应阈值不同。随干旱胁迫加剧,胡杨表观量子效率(AQY)、P_n、LSP与P_(nmax)持续降低,严重干旱胁迫下暗呼吸速率(R_d)、LCP反而明显增大。RSWC45%胡杨仍能保持较高的AQY、P_(nmax)、LSP,RSWC45%其P_(nmax)、LSP显著降低,干旱胁迫显著抑制了胡杨光合进程和光强耐受范围,降低了光合效率,严重干旱胁迫严重影响胡杨苗木的正常生长和光合作用。干旱荒漠环境下,胡杨采取缩窄光照生态幅、降低光能利用率和减少呼吸消耗来积极抵御荒漠干旱逆境伤害的生态对策。因此,从极端干旱荒漠区种群保护与植被恢复角度来看,胡杨林土壤水分应维持在RSWC 50%左右,符合干旱缺水地区植物生长和高效用水的管理原则。     

贝壳砂生境干旱胁迫下杠柳叶片光合光响应模型比较

以黄河三角洲贝壳堤岛3年生杠柳(Periploca sepium)苗木为试验材料, 模拟设置贝壳砂生境下的4种水分梯度, 利用CIRAS-2型光合作用系统测定杠柳叶片在不同干旱胁迫下的光合作用光响应过程, 采用4种光响应模型进行拟合分析, 以比较贝壳砂生境干旱胁迫下适宜的光响应模型, 探讨最佳光响应模型参数对干旱胁迫的适应规律。结果表明: 4种模型对杠柳叶片光合作用光响应过程拟合效果的优劣顺序为: 直角双曲线修正模型>非直角双曲线模型>指数模型>直角双曲线模型, 后3种模型均为没有极值的函数, 故不能很好地拟合光响应曲线光抑制过程, 并不能直接求解最大净光合速率(P_nmax)和光饱和点(LSP)。光响应参数拟合效果最佳表现为: 非直角双曲线模型的暗呼吸速率(R_d), 直角双曲线模型的光补偿点(LCP), 直角双曲线修正模型的P_nmax和LSP。4种光响应模型对干旱胁迫具有不同的适应性, 直角双曲线修正模型适应各种水分条件, 直角双曲线模型和指数模型较适合轻度干旱胁迫条件, 非直角双曲线模型较适合重度干旱胁迫条件。随干旱胁迫的加剧, 光响应参数表观量子效率(AQY)、R_d和LCP先升高后下降, 净光合速率(P_n)、P_nmax和LSP逐渐下降。轻度、中度和重度干旱胁迫下, LSP分别比对照下降5.2%、16.3%和34.5%, P_nmax分别比对照下降17.8%、39.0%和59.0%。水分充足条件下, 杠柳叶片光能利用最强, 光照生态幅最宽; 重度干旱胁迫下, 杠柳叶片表现出明显的光饱和、光抑制现象, 光能利用减弱, 光合能力受到较大限制。     

不同光照环境下荷花叶片光合光响应模型比较

以上海荷花品种‘伯里夫人’为试验材料,设置全光照和林下遮荫(50%全光照)2种不同的光照环境,采用4种光响应模型拟合分析荷花叶片净光合速率光响应过程,比较不同光照下适宜的光响应模型,研究荷花品种对遮荫环境的适应规律.结果表明: 4种模型对荷花叶片光合作用光响应过程拟合效果的优劣顺序为：直角双曲线修正模型>指数模型>非直角双曲线模型>直角双曲线模型,后3种模型均为没有极值的函数,不能直接求得最大净光合速率(P_{n max})和光饱和点(LSP).直角双曲线修正模型对LSP、P_{n max}、暗呼吸速率(R_d)和光补偿点(LCP)等光响应参数表现出最佳的拟合效果,拟合值与实测值相对误差最小.随光强减弱,荷花主要的光合生理参数均降低,其中,R_d下降幅度显著,其他参数变化不显著.说明荷花对适度弱光环境具备一定的适应能力,表现出良好的光合适应性反应与调节,能够维持植株的正常生长.
     

不同淹水时间下中华蚊母树光响应特征及其模型比较

本文模拟库区秋冬季淹水环境,利用Li-6400 XT便携式光合仪测定了淹水条件下2年生中华蚊母树的光响应曲线,并采用直角双曲线模型、非直角双曲线模型和直角双曲线修正模型3种数学模型进行拟合分析,以探讨不同模型对水淹胁迫下中华蚊母树的适用性以及最佳光合参数对水淹胁迫的适应规律.结果表明:非直角双曲线模型对正常水分生长和短期水淹下(水淹15 d)中华蚊母树光响应过程的拟合优于其他两种模型,而直角双曲线修正模型对长期水淹下(水淹30、45和60 d)中华蚊母树光响应过程的拟合更具优势.直角双曲线修正模型对光补偿点(LCP)、最大净光合速率(Pn max)和光饱和点(LSP)的拟合效果最佳,非直角双曲线模型对暗呼吸速率(Rd)的拟合效果最佳.水淹前期(30 d),中华蚊母树表观量子效率(Φ)、Pn max和LSP逐渐降低,而LCP和Rd逐渐升高,但随着水淹时间的继续增加,中华蚊母树逐渐对水淹产生了适应性,各项光合生理指标逐渐趋于稳定,说明中华蚊母树具有一定适应水淹环境的能力.     

光强与水分处理下景宁木兰光合光响应模型拟合比较

采用5种数学模型(直角双曲线模型、非直角双曲线模型、二次函数模型、指数模型、直角双曲线修正模型)对不同光照与水分处理下景宁木兰(Magnolia sinostellata)幼苗光响应过程进行拟合分析,以期筛选出光照与水分胁迫下景宁木兰适宜的光响应模型。结果表明:(1)5种拟合模型对景宁木兰光响应过程拟合精度为:指数模型直角双曲线修正模型直角双曲线模型非直角双曲线模型二次函数模型。(2)光合参数的拟合效果表现为:指数模型对景宁木兰最大净光合速率(Pnmax)、光饱和点(LSP)进行求解较准确,直角双曲线修正模型对光补偿点(LCP)求解最佳,而暗呼吸速率(Rd)的结果采用非直角双曲线模型较为合理。(3)景宁木兰幼苗能适应一定的弱光及流动水环境,而深度遮阴及积水环境抑制景宁木兰幼苗的光合速率。     

亚热带10种蕨类植物光响应模型拟合及光合特性研究

通过合适的光响应模型来准确计算植物光合参数是研究植物光合特性的重要手段。为深入了解亚热带蕨类植物的光合特性,采用直角双曲线模型、非直角双曲线模型、指数模型和直角双曲线修正模型等4种常用光响应模型分别对10种亚热带蕨类植物进行光响应曲线拟合。通过分析决定系数(R~2)、均方根误差(RMSE)、平均绝对误差(MAE)、光饱和点(LSP)、光补偿点(LCP)、最大净光合速率(P_nmax)、暗呼吸速率(R_d)和表观量子效率(AQE)等9种参数,探讨亚热带蕨类植物的光响应模型拟合效果及其光合特性。结果表明：直角双曲线修正模型和非直角双曲线模型对本研究10种亚热带蕨类植物的拟合效果较好,其中直角双曲线修正模型的LSP拟合效果最好,非直角双曲线模型的拟合精度最高。光合参数的聚类分析和TOPSIS(Technique for Order Preference by Similarity to an Ideal Solution)综合评价法表明,10种亚热带蕨类植物的光合特性既具有相似性又存在物种特异性。黑鳞耳蕨(Polystichum makinoi(Tag...     

不同水分条件下胡杨光响应曲线拟合模型比较

本研究通过测量不同水分条件下胡杨（Populus euphratica Oliv.）叶片的光响应曲线,并采用4种光响应模型对其光合特征参数拟合值与实测值进行比较,分析了不同水分条件下光响应曲线模型对胡杨适用性的影响机制。结果表明,当水分供应充足时,胡杨非直角双曲线模型对暗呼吸速率（R_d）的拟合效果最优,直角双曲线修正模型拟合光饱和点（LSP）、最大净光合速率（P_nmax）、光补偿点（LCP）的结果与实测值较接近;但当胡杨受到水分亏缺后,直角双曲线修正模型对P_nmax和光饱和点（LSP）的拟合效果最优,直角双曲线模型对R_d和LCP的拟合效果最佳。因此,水分条件有利时胡杨应用直角双曲线修正模型、非直角双曲线模型较好;水分亏缺条件下采用直角双曲线修正模型、直角双曲线模型更为适合。     

三峡库区消落带不同水淹强度下池杉与落羽杉的光合生理特性

为探究三峡库区消落带原位人工种植的池杉(Taxodium ascendens)和落羽杉(Taxodium distichum)在该特殊生境下的适应机制,设置了浅淹(SS,海拔175m,对照)、中度水淹(MS,海拔170m)和深度水淹(DS,海拔165m)3个水淹处理组,测定了两树种在连续4个周期性水淹处理后的光合响应过程,并采用直角双曲线模型、非直角双曲线模型、直角双曲线修正模型和指数模型进行拟合,比较各模型拟合结果差异并选出最优模型,通过最优模型来分析水淹后落干期两树种的光合生理变化。结果表明:(1)不同模型间的光响应曲线拟合结果存在差异(P0.05)。综合分析可知,4种模型中,指数模型是拟合两树种光响应曲线的最优模型,更符合植物的生理学意义。(2)两树种的光响应曲线有相似的变化规律,光合速率(P_n)的表现均为DS组MS组SS组。(3)中度水淹和深度水淹两树种的最大净光合速率(P_(nmax))、表观量子效率(α)、光饱和点(LSP)均高于浅淹,而光补偿点(LCP)则显著降低。以上结果说明落干生长期两树种对强光和弱光的利用能力增强,水淹对两树种的光合潜力有一定的促进作用,这可能与其遭受水淹胁迫后的自我调节能力和光合补偿机制有关。由此表明,当生境发生不良变化时,植物的适应性变化往往表现为沿着有利于光合作用最大化的方向发展。     

关键生育阶段持续干旱对东北春玉米光合特性的影响

采用持续无补水方式对东北春玉米"丹玉39"拔节至成熟阶段进行干旱胁迫处理,对干旱及复水过程中玉米光合特性进行动态观测,研究净光合速率(P_n)、蒸腾速率(T_r)、气孔导度(G_s)、胞间CO_2浓度(C_i)等光合作用中主要变量以及表观量子效率(AQY)、最大净光合速率(P_(nmax))、光补偿点(LCP)和光饱和点(LSP)等光合参数对干旱过程的响应特征。结果表明:P_n、T_r、G_s和C_i随干旱持续均呈减小趋势,对干旱的响应在抽雄期比拔节期更为明显,T_r比P_n更快,C_i在弱光条件下比强光更敏感;各变量对干旱后复水的响应差异较大,恢复能力随干旱时间的延长而下降,在抽雄期弱于拔节期;经历短期干旱复水后P_n会超过正常植株;T_r对复水的响应滞后于P_n,恢复能力弱于P_n;C_i对干旱后复水的恢复在强光下更为敏感;各光合参数中,随干旱加重,AQY先增大后减小;P_(nmax)不断减小且响应速度加快,对复水的恢复能力逐渐下降;LCP和LSP分别呈增大和减小趋势;除LCP与土壤湿度呈显著负相关关系外,AQY、LSP、P_(nmax)以及光合作用可利用光强范围均随土壤湿度增大而显著增大。     

几种光合作用光响应典型模型的比较研究

光响应曲线是判定植物光合效率的重要方法,通过曲线可以获得植物光合特性的相关生理参数,但不同模型提取的光响应参数和指标存在差异。本文选择直角双曲线、非直角双曲线和两种指数曲线模型,分别对3个品系常绿杨光响应数据进行拟合,提取了各光响应曲线模型的主要特征参数,对比分析了各模型参数问的差异,并对光饱和点（LSP）的不同计算方法进行了讨论。最后用巨尾桉光响应数据对分析结果作了进一步验证。结果表明,直角和非直角双曲线模型拟合的最大净光合速率（P＇max）、表观量子效率（a）及暗呼吸速率（Rd）值高于指数模型拟合值,且直角双曲线拟合的各参数均比非直角双曲线拟合的各参数的值大,而两指数模型各参数拟合值基本一致;在LSP计算方法中,用光通量200μmol·m^-2·s^-1以下的点拟合的Pn-I直线与其它模型相结合得到光饱和点的方法不可靠,会使计算结果明显偏小,用接近最大总光合速率Pmax一定比例的方法估计LSP也存在较大偏差,而P＇max由于消除了Rd的影响,计算光饱和点时各模型的估计比例相对固定,是一个比较理想的LSP估计方法,初步得出直角、非直角及指数模型用P＇max来估计光饱和点时应选取的比例分别为（78±1）％、（82±1）％及（96±1）％。     

亚热带森林演替阶段下不同光环境对芒萁光合生理的影响

光环境的变化是群落演替进程中植物进入和退出群落的重要因素。为研究亚热带森林次生演替不同阶段的光照对芒萁光合生理的影响，对灌草丛、马尾松林和常绿阔叶林这3种群落内盆栽芒萁的光响应过程和叶绿素荧光诱导动力学参数进行了研究。结果表明：芒萁在光强为400μmol m^-2 s^-1左右且日变化幅度较小的马尾松林下净光合速率(P_n)最高，在光强50μmol m^-2 s^-1左右的常绿阔叶林下次之，在400—1800μmol m^-2 s^-1左右波动的灌草丛内最低。这是因为灌草丛内芒萁J点相对可变荧光(V_j)、K点标准化后的相对可变荧光(W_k)显著升高，以吸收光能为基础的光系统Ⅱ性能指数(PSⅡ)(PI_ABS)显著降低，而热耗散参数(φ_Do)基本不变，即强光破坏了芒萁光合机构PSⅡ的供体侧和受体侧，使其产生了光抑制。常绿阔叶林内芒萁叶绿素荧光诱导动力学参数与马尾松林下...     

Light responses ofBeggiatoa

Studies on nativeBeggiatoa demonstrated diel vertical migration into, and out of, sediments at the bottom of warm spring pools. Laboratory experiments withBeggiatoa in natural sediments suggested that high light was the cause of the downward movement. The nature of this presumed photomotion was clarified by microscopic observation of individual filaments of nativeBeggiatoa at light/dark boundaries where the light was varied in intensity and quality. Using white light, a negative photo-response was demonstrated, and a dose-response curve was constructed which indicates an increasing response to light over three orders of magnitude of intensity. A coarse action spectrum implicated a pigment with a peak in the blue region as the receptor. Pure culture studies showed the negative response to be a step-up phobic one. The light intensity increase necessary to invoke reversals was a smaller percentage of the initial intensity for higher initial intensities. The light intensity levels and gradient strengths necessary to evoke reversals in single filaments were consistent with the hypothesis that the step-up response accounts for the disappearance in the field. This response has adaptive significance since full sunlight was completely inhibitory toBeggiatoa growth, even when filaments were aggregated in tufts. Dilute suspensions were also inhibited by as little as 5000 lux (fluorescent lamps).     

Effects of microbeam light on growth and phototropism ofPilobolus crystallinus sporangiophores

A small blue-light beam (50 μm in diam) was used to examine light-growth response and phototropism inPilobolus crystallinus sporangiophores. Continuous irradiation by microbeam of a region 100–150 μm from the apex promoted the growth of a dark-adapted sporangiophore for about 15 min after a lag period of 1–2 min. After the promotion, the growth rate fell below that before the irradiation. Irradiation of the apex of sporangiophore slightly promoted the growth but strongly inhibited the growth after the promotion. A smaller light beam (10 μm in diam) applied continuously at grazing incidence along one side of the sporangiophore caused bending toward the shaded side, implying that the irradiated side grew more rapidly than the shaded side and that the lens effect is involved in the phototropism of young sporangiophores ofP. crystallinus. The involvement of the lens effect was confirmed by the fact that a carotenoid-less mutant was 1.5–2 times more sensitive to unilateral blue light than the wild type, probably because of a smaller intracellular light attenuation during passage through the mutant cell.     

种源地气候对蒙古莸光响应特性的影响

植物对环境的长期适应所形成的遗传特性对其光合、生长等有着重要影响。通过测定8种不同种源地蒙古莸在相同环境条件下的光响应曲线,分析、比较了不同种源地蒙古莸光合响应参数的差异及种源地气候对其影响大小,以期了解蒙古莸光合特性响应环境变异的机理。结果表明:(1)在相同环境条件下,蒙古莸的光合能力与其种源地有密切关系。随种源地从东到西、从北到南,光合能力逐渐降低,其中内蒙古苏尼特左旗、二连浩特种源的最大净光合速率(Pnmax)最高,甘肃民勤种源Pnmax最小。(2)种源地气候对蒙古莸光响应特性有着显著影响,其中温度和海拔是主要因素,温度、海拔与最大净光合速率(Pnmax)、暗呼吸速率(Rd)均显著负相关(P0.01)。(3)种源地气候对各个光合参数的解释程度为:16.65%—73.52%,对表观量子效率(α1)、最大净光合速率(Pnmax)、光补偿点(Ic)和暗呼吸速率(Rd)有着重要影响,解释力均大于40%。由此可见,种源地气候差异引起的遗传变异是造成不同种源间光响应特性差异的重要因素之一。不同种源蒙古莸光合能力的差异是其适应特有环境的体现。     

Phototropic fluence-response relations for Avena coleoptiles on a clinostat

Phototropism of Avena sativa L. has been characterized using a clinostat to negate the gravitropic response. The kinetics for development of curvature was measured following induction by a single pulse of blue light (BL), five pulses of BL at 20-min intervals, and this same pulsed-light regime following a 2-h red light (RL) pre-irradiation. A final curvature of about 14° is expressed within 180 min following the single pulse; a final curvature of about 62° in about 240 min following five pulses without pre-irradiation; and a curvature of over 125° in 360 min following five pulses after the RL pre-irradiation. For seedlings not pre-irradiated, the final curvature to five pulses of BL at a total fluence of 9.4 pmol·cm^-2 increases with time of darkness between pulses up to 15 min; with seedlings pre-irradiated with RL, curvature increased more slowly with time of darkness between pulses to a maximum at 35 min. The final curvature induced by a constant fluence of 9.4 pmol·cm^-2 increases linearly with time between the first pulse and last pulse of a five-pulse sequence. The curvature induced by a single BL pulse with a 5-min RL co-irradiation increases with fluence to a maximum of about 60° at about 10 pmol·cm^-2, and then decreases to 0° at about 200 pmol·cm^-2. Curvature induced by five BL pulses following a 2-h RL pre-irradiation increased with fluence from a threshold of about 0.05 pmol·cm^-2 to a maximum of 90° at about 10 pmol·cm^-2, and then gradually decreased with fluence to 50° at 1 000 pmol·cm^-2. Based on these data, it is concluded that the initial photoproduct formed by a BL pulse has a limited lifetime, that there is a kinetic limitation downstream of the photoreceptor pigment for phototropism, and that the additivive effect of pulsed BL is distinct from the potentiating effect of RL on phototropism. Thus, any degree of curvature from 0° to over 90° may be induced by a fluence in the ascending arm of what is traditionally called the first positive phototropic response.Abbreviations BL blue light - RL red light     

A single positive phototropic response induced with pulsed light in hypocotyls of Arabidopsis thaliana seedlings

The fluence-response curves were measured for phototropic curvature in response to unilateral 450-nm light in hypocotyls of Arabidopsis thaliana (L.) Heynh. These show the classical first positive (peak curvature of 9–10°), indifferent and second positive phototropic response. Reciprocity is valid only for the first positive response; the fluence requirements for its induction are similar to those for induction of the first positive phototropic response of coleoptiles. Large angles of curvature also may be induced by multiple pulses if the individual pulses are separated by an optimum dark period of about 15 min. The curvature induced by a given fluence, whether applied in continuous irradiation or a sequence of pulses, is a linear function of the duration of continuous irradiation or the duration between first and last pulse, respectively. For a given fluence applied in a sequence of pulses, reciprocity remains valid provided the duration between first and last exposure is kept constant. When the duration between first and last pulse is sufficiently long, the fluence required for high phototropic curvature falls in the first positive fluence range. These results are interpreted to indicate the existence of a kinetic limitation in the transduction sequence, and a relatively short lifetime of an initial physiologically active photoproduct. The apparent existence of more than one positive response may have resulted from these characteristics of the transduction sequence.     

7个光响应曲线模型对不同植物种的实用性

光响应曲线研究方法被广泛应用在植物生理的研究中,但是在应用光响应模型拟合光响应数据时,往往只考虑到研究的目的,很少考虑到模型是否适用于所研究的植物。本文通过采用7个不同的光响应模型对白桦叶片和兴安落叶松针叶光响应曲线数据拟合的比较,发现不同模型对同一种植物光响应曲线的拟合结果存在着差异,同一模型对同种植物不同部位叶片光响应曲线的拟合效果也不同,所以在研究植物的光响应时,应考虑到所选光响应模型对该种植物的光响应情况的描述是否恰当。根据具体情况选择最佳模型,以最大限度地保证估测生理指标结果的精确性。     

Strong-light response of Micrasterias thomasiana Archer

Prostrate cells of Micrasterias thomasiana Archer were irradiated from above with intensive blue light. Many of the cells reacted by rising to a profile position. During a period of 15 to 90 min the response is linearly dependent on the duration of irradiation, inferred from the number of rising cells. In a range from 10 to 30 mol m^-2 s^-1 (equalling 2.7–8.0 W m^-2 at a wavelength of 450 nm) and for an irradiation time of 30 min, the rising reaction was linearly dependent on the quantum flux density. Choosing 30 min irradiation time and a quantum flux density of 30 mol m^-2 s^-1, the reactive number of rising cells was employed in establishing an action spectrum. As a result of this, a flavin is postulated as the light-percepting pigment in the reaction, whereas chlorophylls do not appear to be involved. The rising reaction can be distinguished from other light-induced movements as a strong-light response, resembling in this respect the movement of chloroplasts within cells. The different sensitivity of individual cells and the importance of this strong-light response for the algal cells is discussed.     

Action spectra of the light-growth response in three behavioral mutants of Phycomyces

Null-point action spectra of the light-growth response were measured for three mutants of Phycomyces blakesleeanus (Burgeff) and compared with the action spectrum of the wild type (WT). The action spectrum for L150, a recently isolated night-blind mutant, differs from the WT spectrum. The L150 action spectrum has a depression near 450 nm and small alterations in its long-wavelength cutoff, the same spectral regions where its photogravitropism action spectrum is altered. This indicates that the affected gene product influences both phototropism and the light-growth response. For L85, a hypertropic (madH) mutant, the light-growth-response action spectrum is very similar to that of WT even though the photogravitropism action spectrum of L85 has been shown previously to be altered in the near-UV region. The affected gene product in this mutant appears to affect phototropic transduction but not light-growth-response transduction. The action spectrum of C110, a stiff (madE) mutant, differs significantly from the WT spectrum near 500 nm, the same spectral region where sporangiophores of madE mutants have been shown to have small alterations in second-derivative absorption spectra. This indicates that the madE gene product may be physically associated with a photoreceptor complex, as predicted by system-analysis studies.Abbreviations SE standard error of the mean - UV ultraviolet light - Wt wild type I dedicated to Masaki Furuya on the occasion of his 65th birthdayWe thank H. Reiner Schaefer for performing some of the experiments and for help in data analysis, David Durant for computer programming, and Benjamin Horwitz for helpful discussions. This work was supported by a grant from the National Institutes of Health (GM29707) to E.D. Lipson.     

盐分胁迫下杠柳叶片光合特性的光响应研究

利用CID型便携式光合作用仪测定不同NaCl浓度下杠柳叶片净光合速率(P_n)、蒸腾速率(T_r)、气孔导度(G_s)、水分利用效率（WUE）及光能利用率(LUE)生理参数的光响应过程,阐明盐分胁迫下其对光照响应的规律,探讨有利于杠柳正常生长的盐分浓度和光照条件。结果表明:（1）各盐分浓度下杠柳叶片光补偿点（LCP）在21.89～65.05 μmol·m^-2·s^-1之间变动,介于阴性植物与阳性植物之间;杠柳随土壤盐分的不同,其光合作用参数对光照强度表现出一定的适应性和可塑性;50 mmol·L^-1盐分浓度下杠柳光合同化能力最强,最有利于其干物质的积累,表现出一定的耐盐性。（2）轻度的盐分胁迫（小于50 mmol·L^-1）可以提高杠柳叶片的P_n、G_s、WUE和LUE,而盐分胁迫对杠柳的T_r有抑制作用,并随着盐分浓度的增加其抑制作用愈强烈。（3）维持杠柳正常生长的土壤盐分浓度小于50 mmol·L^-1,最佳PAR为1 000～2 000 μmol·m^-2·s^-1;而保持杠柳最大WUE和LUE的光照强度分别为800和100 μmol·m^-2·s^-1。