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1.
胡杨叶片气孔导度特征及其对环境因子的响应   总被引:19,自引:2,他引:17  
依据2005年对极端干旱区荒漠河岸林胡杨的观测资料,对胡杨气孔运动进行了分析研究以揭示胡杨的水分利用特征与抗旱机理。结果表明:(1)胡杨叶片气孔导度日变化呈现为周期波动曲线,其波动周期为2 h,傍晚(20:00)波动消失;净光合速率和蒸腾速率与气孔导度的波动相对应而呈现同步周期波动。(2)胡杨的阳生叶气孔导度高于阴生叶,且不同季节气孔导度值不同,阳生叶气孔导度的季节变幅大于阴生叶。(3)胡杨气孔导度与气温、相对湿度和叶水势有显著相关关系,当CO2浓度较小时,胡杨气孔导度随CO2浓度的增加而增加,当CO2浓度达到一定值后气孔导度不再增加,反而随CO2浓度的增加大幅度降低。(4)胡杨适应极端干旱区生境的气孔调节机制为反馈式反应,即由于叶水势降低导致气孔导度减小,从而减少蒸腾耗水,达到节约用水、适应干旱的目的,表明胡杨的水分利用效率随气孔限制值的增大而减小,二者呈显著负相关。  相似文献   

2.
''金光杏梅''叶片净光合速率与生理生态因子的关系   总被引:13,自引:3,他引:10  
以‘金光杏梅’成熟叶片为试验材料,采用CI-301型便携式CO2气体分析仪测定了其叶片净光合速率(Pn)日变化,并通过多元逐步回归和通径分析方法探讨了净光合速率与生理生态因子间的关系。结果表明:‘金光杏梅’叶片净光合速率日变化为双峰曲线,在上午10:00和下午15:00分别出现一次高峰,具有典型的"午休"现象,它是由气孔因素和非气孔因素两种因素造成的;叶片气孔导度和蒸腾速率日变化均与净光合速率日变化呈正相关,回归方程分别为yPn=0.947xGs2 0.2874xGs 57.945,(R2=0.8534)和yPn=0.8079xTr0.5421,(R2=0.5716);影响‘金光杏梅’叶片净光合速率的主要生态因子是光合有效辐射和大气CO2浓度,主要生理因子是气孔导度和蒸腾速率。  相似文献   

3.
米槁幼苗光合作用及光响应曲线模拟对干旱胁迫的响应   总被引:5,自引:0,他引:5  
为阐明米槁光合作用对干旱胁迫的响应规律与适应机制,以一年生米槁幼苗为研究对象,进行盆栽试验研究设置3种不同土壤含水量梯度,利用Li-6400便携式光合作用系统测定干旱胁迫下的光合生理指标及光响应过程,光响应曲线模拟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进行拟合并对比,以期选出适用于干旱环境下的光响应模型。结果表明(1)光响应曲线模型对干旱胁迫下米槁幼苗的光合作用拟合中直角双曲线、非直角双曲线和指数模型适用于低光合有效辐射(PAR),但拟合光响应参数与实测值相差大,只有直角双曲线修正模型能够很好的拟合各个处理且拟合参数比较精确米槁幼苗。(2)光合作用的表观量子效率(Φ)小于一般植物的光合量子效率,则其对弱光的光能利用效率相对较低。(3)在较强的光合有效辐射条件下,严重干旱胁迫下的米槁净光合速率P_n显著下降,出现了明显的光抑制现象;中度胁迫下净光合速率(P_n)、最大净光合速率(P_(nmax))、光补偿点(LSP)最大,米槁具有较宽的抗旱适应范围,有一定的抗旱性;严重胁迫下P_n、P_(nmax)、LSP降低,蒸腾速率(T_r)与气孔导度(G_s)下降幅度更大,但仍具有较高的水分利用效率(WUE),米槁在严重的干旱胁迫下光合机构受到一定的损伤,但自身可以通过生理调节来积极适应不良环境,减少光合机构伤害。(4)综合来看,在人工管理或种植米槁时,为了适应米槁生长发育,建议土壤含水量保持在23.05%到14.92%之间。  相似文献   

4.
不同水分条件下胡杨光响应曲线拟合模型比较   总被引:1,自引:0,他引:1       下载免费PDF全文
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(Rd)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(Pnmax)、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Pnmax和光饱和点(LSP)的拟合效果最优,直角双曲线模型对Rd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。  相似文献   

5.
小麦拔节期淹水对叶片光合特性的影响   总被引:3,自引:0,他引:3  
为研究拔节期涝害对小麦叶片光合特性的影响,以小麦品种烟农19为试验材料,采用盆栽试验,于小麦拔节期进行淹水(涝害)处理,分析小麦叶片光合气体交换参数的变化。结果表明,拔节期淹水6 d后小麦叶片SPAD值较对照显著下降。在淹水3–9 d内,随着小麦叶片净光合速率逐渐下降,叶片气孔导度和胞间CO_2浓度亦显著下降,说明烟农19光合速率下降主要是叶片气孔限制引起的。而在淹水后期(9d之后),净光合速率持续下降,而叶片胞间CO_2浓度却升高,说明在涝害发生后期叶片光合速率下降主要由非气孔因素引起。在小麦拔节期涝害前期叶片光合速率下降主要是由叶片气孔限制引起的,而在涝害发生后期叶片光合速率下降主要由非气孔因素引起。  相似文献   

6.
塔里木河中游胡杨与灰叶胡杨气体交换特性对比研究   总被引:1,自引:0,他引:1  
在自然条件下利用Li-6400光合作用系统对塔里木河中游地区的天然胡杨、灰叶胡杨净光合速率(Pn)、气孔导度(Gs)、胞间CO2浓度(Ci)、蒸腾速率(Tr)和水分利用效率(WUE)等生理指标进行测定分析,探讨它们对外界干旱环境适应的生理特性,为进一步研究胡杨、灰叶胡杨的光合水分生理特性,以及保护恢复塔里木河流域的天然胡杨林提供依据。结果表明:(1)在整个光合日变化进程中,胡杨的日平均Pn、Gs、Tr以及WUE均高于灰叶胡杨。(2)胡杨和灰叶胡杨的净光合速率日变化均呈"双峰"曲线并存在光合"休眠"现象。(3)胡杨、灰叶胡杨在正午时分出现的Pn下降主要是受到气孔限制的影响既气孔限制值增大、胞间CO2浓度减小;傍晚时分出现的光合速率下降主要是因受到外界光照强度减弱,既受非气孔限制影响较大。(4)决定胡杨和灰叶胡杨Pn日变化的环境因子作用大小均为:光量子通量密度(PPFD)>气孔导度(Gs)>空气相对湿度(RH)>气温(Tair);决定胡杨与灰叶胡杨Tr日变化的环境因子作用大小顺序分别为:气温(Tair)>光量子通量密度(PPFD)>气孔导度(Gs)>空气相对湿度(RH)和光量子通量密度(PPFD)>气温(Tair)>气孔导度(Gs)>空气相对湿度(RH)。研究认为,胡杨与灰叶胡杨为适应干旱半干旱区的环境,在长期适应过程中形成了不同的生理生态对策,胡杨主要是通过调节Gs来有效控制蒸腾失水,提高WUE,进而适应干旱环境;灰叶胡杨主要是通过高蒸腾耗水,降低WUE来减少干旱环境对自身的伤害。  相似文献   

7.
羊草气孔导度的Jarvis-类模型   总被引:4,自引:2,他引:2  
牛海山  旭日  张志诚  陈佐忠 《生态学杂志》2005,24(11):1287-1290
在干旱半干旱气候条件下,土壤水分状况通常是决定植物气孔导度的重要因素,现有气孔导度模型Jarvis-类和耦合模型(或光合-导度模型)未充分考虑这一因素对气孔导度的影响。本文以Jarvis气孔导度模型为基础,提出一个充分考虑土壤水分状况因素的气孔导度模型。该模型对羊草连续两年(1998~1999)野外实地观测结果拟合良好(R2=0.603),预测能力较线性回归方程(R2=0.361)有明显提高。  相似文献   

8.
四种水稻品种的光合光响应曲线及其模型拟合   总被引:12,自引:0,他引:12  
应用4种典型的光响应模型对4个水稻品种“02428”、“淦鑫688”、“JR8892-1”和“JR8892-2”叶片的光合光响应曲线进行了拟合.结果表明:直角双曲线模型、非直角双曲线模型、指数函数以及修正的直角双曲线模型对4个水稻品种的光合光响应曲线都可以进行拟合,决定系数均为R2 >0.99.但只有修正的直角双曲线模型可以拟合发生光抑制部分的光响应曲线,且可直接计算其饱和光强(Isat);由各模型计算的光合参数可知,直角双曲线模型、非直角双曲线模型求得的最大净光合速率(Pnmax)远高于实测值,指数函数与修正的直角双曲线模型求得的Pnm.与实测值最为接近;直角双曲线、非直角双曲线模型以及指数函数求得的Isat均与实测值相差较大,除了“JR8892-1”采用指数函数求得的Isat大于实测值外,其余3个品种用上述3种模型拟合求得的Isat均小于实测值,唯有修正的直角双曲线模型求得的Isat与实测值最为相符;对于低光强部分的参数光补偿点(Ic)与暗呼吸速率(Rd),修正的直角双曲线模型最接近其测量值;不同水稻品种的光合特性,“JR8892-1”饱和光强与最大净光合速率明显高于高光效品种“02428”;处于分蘖盛期的“JR8892-2”也表现出较高的饱和光强和最大净光合速率,而超级稻“淦鑫688”相对于其他品种,则具有较低的暗呼吸速率,光合产物消耗少.  相似文献   

9.
胡杨、灰叶胡杨光合及叶绿素荧光特性的比较研究   总被引:42,自引:10,他引:32  
比较研究了两年生胡杨和灰叶胡杨叶片的光合及叶绿素荧光特性.结果表明:胡杨和灰叶胡杨均表现出净光合速率(Pn)日变化呈单峰曲线,只是在12:00时胡杨的Pn略微降低;气孔导度日变化均呈单峰型曲线;胞间CO2浓度日变化呈近“V”字型曲线.相同的试验条件下,胡杨的净光合速率、气孔导度高于灰叶胡杨,净光合速率与气孔导度峰值出现在上午10:00时;胡杨胞间CO2浓度低于灰叶胡杨,胞间CO2浓度最低值均出现在中午14:00时.经充分暗适应后的叶片叶绿素荧光参数初始荧光、PSⅡ原初光能转换效率和PSⅡ潜在活性均为胡杨显著大于灰叶胡杨.以太阳光为光化学光,测定的叶绿素荧光参数日变化显示,胡杨PSⅡ实际的光化学反应量子效率、非循环电子传递速率、光化学猝灭系数均大于灰叶胡杨,而非光化学猝灭系数却较灰叶胡杨小.胡杨与灰叶胡杨在光合与叶绿素荧光特性上的差异,是胡杨更能适应干旱荒漠区高光、高温与低相对空气湿度环境,从而表现出高净光合速率的部分生理学原因之一.  相似文献   

10.
利用便携式光合蒸腾仪于夏季、秋季各测定了国家重点保护植物丹霞梧桐(Firmiana danxiaensis Huse et H.S.Kiu)叶片的光合特性及生态因子,以期为了解该植物的生态适应性提供基础数据。结果表明:夏季测定日的气温、大气相对湿度、CO_2浓度、光合有效辐射、叶片SPAD值、净光合速率、蒸腾速率及气孔导度等光合特性等指标均高于秋季测定日的相应值,但叶片水分利用效率、各因子之间的相关性则夏季低于秋季。夏季在测定日平均气温近37.37℃高温下,大气相对湿度65.66%,丹霞梧桐叶片净光合速率平均为14.35μmol CO_2/m~2·s,蒸腾速率4.28 mmol H_2O/m~2·s,气孔导度184.33 mol H_2O/m~2·s;秋季测定日气温平均33.78℃,大气相对湿度41.97%,叶片净光合速率8.70μmol CO_2/m~2·s,蒸腾速率2.75 mmol H_2O/m~2·s,气孔导度85.19 mol H_2O/m~2·s;可见,丹霞梧桐在夏季以高的净光合速率、蒸腾速率和气孔导度,表现出对丹霞地貌高温高湿环境的高度适应性。  相似文献   

11.
羊草叶片气孔导度特征及数值模拟   总被引:20,自引:3,他引:17  
对松嫩平原草地羊草叶片气孔导特征及与环境因子关系的研究结果表明,羊草叶片气孔导度日变化与环境因子密切相关,晴天表现为双峰曲线,阴天为单峰曲线,同时叶片气孔导度(gs)对瞬时光合有效辐射(PAR),叶片与空气间的水汽压亏损(VPD),空气温度(Ta)反应十分明显,依据野外实测资料,在对国际上两类代表性气孔导度模型验证比较的基础上,建立了适用于羊草草原的羊草叶片气孔导度对环境因子的响应模型gs=PAR(2.01Ta^2 147.74Ta-2321.11)/(444.62 PAR)(-538.04 VPD).  相似文献   

12.
Zeiger E  Field C 《Plant physiology》1982,70(2):370-375
The photocontrol of the functional coupling between photosynthesis and stomatal conductance in the leaf was investigated in gas exchange experiments using monochromatic light provided by lasers. Net photosynthesis and stomatal conductance were measured in attached leaves of Malva parviflora L. as a function of photon irradiance at 457.9 and 640.0 nanometers.

Photosynthetic rates and quantum yields of photosynthesis were higher under red light than under blue, on an absorbed or incident basis.

Stomatal conductance was higher under blue than under red light at all intensities. Based on a calculated apparent photon efficiency of conductance, blue and red light had similar effects on conductance at intensities higher than 0.02 millimoles per square meter per second, but blue light was several-fold more efficient at very low photon irradiances. Red light had no effect on conductance at photon irradiances below 0.02 millimoles per square meter per second. These observations support the hypothesis that stomatal conductance is modulated by two photosystems: a blue light-dependent one, driving stomatal opening at low light intensities and a photosynthetically active radiation (PAR)-dependent one operating at higher irradiances.

When low intensity blue light was used to illuminate a leaf already irradiated with high intensity, 640 nanometers light, the leaf exhibited substantial increases in stomatal conductance. Net photosynthesis changed only slightly. Additional far-red light increased net photosynthesis without affecting stomatal conductance. These observations indicate that under conditions where the PAR-dependent system is driven by high intensity red light, the blue light-dependent system has an additive effect on stomatal conductance.

The wavelength dependence of photosynthesis and stomatal conductance demonstrates that these processes are not obligatorily coupled and can be controlled by light, independent of prevailing levels of intercellular CO2. The blue light-dependent system in the guard cells may function as a specific light sensor while the PAR-dependent system supplies a CO2-modulated energy source providing functional coupling between the guard cells and the photosynthesizing mesophyll.

  相似文献   

13.
The effect of soil flooding on photosynthesis, transpiration and stomatal conductance of Jatropha curcas seedlings were studied under natural environmental variables. Soil flooding reduced photosynthesis (P N), transpiration (E) and stomatal conductance (gs) in response to leaf positions of Jatropha curcas plants. Based on the results, we conclude that decrease in stomatal opening and stomatal limitation of photosynthesis, followed by decrease in individual leaf area are the main causes of reductions in carbon uptake of flooded seedlings. A mathematical relationship was successfully developed to describe photosynthesis, transpiration and stomatal response of Jatropha under soil flooding stress.  相似文献   

14.
Photosynthesis and water efflux were measured in different PAR and stomatal conductance in members of Avicenniaceae and Rhizophoraceae. Trend of leaf temperature with irradiance and its effect on photosynthesis were also estimated. In most of the studied species, photosynthesis and stomatal conductance followed similar trends with increase in irradiance. The rate of net photosynthesis and stomatal conductance were higher in members of Avicenniaceae than in Rhizophoraceae. In Avicenniaceae, the optimum PAR for maximum photosynthesis ranged between 1340–1685 (μmol m-2s-1, which was also higher than that of Rhizophoraceae (840-1557 μmol m-2s-1). Almost in all the studied taxa, transpiration and stomatal conductance followed similar trends and reached the maximal peaks at the same PAR value. The range of breakeven leaf temperature was almost the same in both the families (34-36°C in Avicenniaceae and 33.5-36.3°C in Rhizophoraceae), beyond which assimilation rate declined.  相似文献   

15.
Aerial parts of lettuce plants were grown under natural tropical fluctuating ambient temperatures, but with their roots exposed to two different root-zone temperatures (RZTs): a constant 20 degrees C-RZT and a fluctuating ambient (A-) RZT from 23-40 degrees C. Plants grown at A-RZT showed lower photosynthetic CO2 assimilation (A), stomatal conductance (gs), midday leaf relative water content (RWC), and chlorophyll fluorescence ratio Fv/Fm than 20 degrees C-RZT plants on both sunny and cloudy days. Substantial midday depression of A and g(s) occurred on both sunny and cloudy days in both RZT treatments, although Fv/Fm did not vary diurnally on cloudy days. Reciprocal temperature transfer experiments investigated the occurrence and possible causes of stomatal and non-stomatal limitations of photosynthesis. For both temperature transfers, light-saturated stomatal conductance (gs sat) and photosynthetic CO2 assimilation (A(sat)) were highly correlated with each other and with midday RWC, suggesting that A was limited by water stress-mediated stomatal closure. However, prolonged growth at A-RZT reduced light- and CO2-saturated photosynthetic O2 evolution (Pmax), indicating non-stomatal limitation of photosynthesis. Tight temporal coupling of leaf nitrogen content and P(max) during both temperature transfers suggested that decreased nutrient status caused this non-stomatal limitation of photosynthesis.  相似文献   

16.
Whole-plant hydraulic conductance, shoot growth, and leaf photosynthetic properties were measured on kiwifruit vines with four clonal rootstocks to examine the relationship between plant hydraulic conductance and leaf stomatal conductance (gs) and to test the hypothesis that reduced hydraulic conductance can provide an explanation for reductions in plant vigour caused by rootstocks. The rootstocks were selected from four species of Actinidia and grafted with Actinidia chinensis var. chinensis 'Hort16A' (yellow kiwifruit) as the scion. Total leaf area of the scion on the least vigorous Actinidia rootstock, A. kolomikta, was 25% of the most vigorous, A. hemsleyana. Based on shoot growth and leaf area, the selections of A. kolomikta and A. polygama are low-vigour rootstocks, and A. macrosperma and A. hemsleyana are high-vigour rootstocks for A. chinensis. Whole-plant hydraulic conductance, the ratio of xylem sap flux to xylem water potential, was lower in the low-vigour rootstocks, reflecting their smaller size. However, leaf-area-specific conductance (Kl) and gs were both higher in the low-vigour rootstocks, the opposite of the expected pattern. Differences in Kl were found in the compartment from the roots to the scion stem, with no difference between rootstocks in the conductance of stems or leaves of the scion. There was no evidence that the graft union caused a significant reduction in hydraulic conductance of vines with low-vigour rootstocks. Leaf photosynthetic capacity did not vary between rootstocks, but photosynthesis and carbon isotope discrimination (Delta13C) under ambient conditions were higher in the low-vigour rootstocks because gs was higher. gs and Delta13C were positively correlated with Kl, although the mechanism for this relationship was not based on stomatal regulation of a similar xylem water potential because water potential varied between rootstocks. For Actinidia rootstocks, changes in Kl do not provide a direct explanation for changes in vigour of the scion. However, depending on the rootstock in question, changes in hydraulic conductance, biomass partitioning, and crown structure are involved in the response.  相似文献   

17.
植物叶片最大羧化速率及其对环境因子响应的研究进展   总被引:3,自引:0,他引:3  
张彦敏  周广胜 《生态学报》2012,32(18):5907-5917
植物叶片最大羧化速率对环境因子的响应关系是陆地生态系统生产力与碳收支研究的重要方面。论文从测定方法、影响因子与模拟模型3方面综述了植物叶片最大羧化速率及其对环境因子响应研究的最新进展,指出现有的植物叶片最大羧化速率对单个环境因子的响应研究严重制约着陆地生态系统生产力的准确评估。为弄清植物叶片最大羧化速率对环境因子的综合响应关系,迫切需要加强以下研究:(1)植物叶片最大羧化速率的生物与环境控制机制研究;(2)生物与环境因子协同作用下的植物叶片最大羧化速率定量模拟及其尺度化研究;(3)植物叶片最大羧化速率的环境因子阈值研究。  相似文献   

18.
Fourteen genotypes of barley were compared for response to salinity by monitoring the parameters gas exchange and chlorophyll fluorescence. We present relationships between stomatal conductance (gs) gas exchange chlorophyll fluorescence parameters and aboveground dry matter (AGDM). We found that genetic variability provided a continuum of data for gs across control and saline conditions. We used this continuum of gs values to test the overall relationships between gs and net photosynthesis (A), leaf internal CO2 concentration (Ci), actual quantum yield of PSII electron transport (PhiPSII), relative electron yield over net CO2 assimilation rate (ETR/A), and AGDM. The relationship between gs and A was highly significant (P < 0.0001) for both control and saline treatments, while correlations between gs and Ci, and Ci and A were significant only under control conditions. Unexpectedly, we found positive correlations between gs and PhiPSII (P < 0.0001) for both conditions. A comparison between relationships of gs and A, and gs and PhiPSII seemed to indicate a possible acclimation to salinity at the chloroplastic level. Finally, the relationships between gs and ETR/A were exceptionally strong for both growing conditions (P < 0.0001) indicating that, as gs values were negatively affected in barley by genetics and salinity as main or interactive effects, there was a progressive increase in photorespiration in barley. Overall, we found that stomatal conductance was a key parameter in the study of barley responses to limiting situations for photosynthesis. We also found a strong relationship between AGDM and gs regardless of growing conditions and genotypes. For breeding evaluations to select barley genotypes for salinity tolerance, it may be possible to replace all measurements of gas exchange and chlorophyll fluorescence by the simple use of a porometer.  相似文献   

19.
气孔导度对CO_2浓度变化的模拟及其生理机制   总被引:2,自引:0,他引:2  
王建林  温学发 《生态学报》2010,30(17):4815-4820
基于气孔运动的生理生化机制重点进行了气孔导度(gs)对CO2浓度变化的响应机制分析,并推导得到气孔导度(gs)对CO2浓度变化响应模型,并以9种植物进行了模型验证。结果表明:随着CO2浓度的升高,气孔导度会逐渐降低,且下降的幅度会随着CO2浓度的升高而逐渐减弱。气孔导度对CO2浓度(Cs)变化的响应模型可以表达为gs=gmax/(1+Cs/Cs0),其中式中gmax是最大气孔导度和Cs0是实验常数。该模型较好地模拟了气孔导度随CO2浓度变化的规律,模型参数具有明确的生理意义,与Jarvis模型和Ball-Berry模型相比,该模型如何实现多种环境因子的耦合有待进一步突破。另外,模型是在短期改变叶片CO2浓度的条件下得出的,在CO2浓度长期胁迫下的适用性也有待进一步确认。  相似文献   

20.
Potatoes (Solanum tuberosum L., cv. Bintje) were grown in a naturally lit glasshouse. Laboratory measurements on leaves at three insertion levels showed a decline with leaf age in photosynthetic capacity and in stomatal conductance at near saturating irradiance. Conductance declined somewhat more with age than photosynthesis, resulting in a smaller internal CO2 concentration in older relative to younger leaves. Leaves with different insertion number behaved similarly. The changes in photosynthesis rate and in nitrogen content with leaf age were closely correlated. When PAR exceeded circa 100 W m–2 the rate of photosynthesis and stomatal conductance changed proportionally as indicated by a constant internal CO2 concentration. The photosynthesis-irradiance data were fitted to an asymptotic exponential model. The parameters of the model are AMAX, the rate of photosynthesis at infinite irradiance, and EFF, the slope at low light levels. AMAX declined strongly with leaf age, as did EFF, but to a smaller extent. During drought stress photosynthetic capacity declined directly with decreasing water potential (range –0.6 to –1.1 MPa). Initially, stomatal conductance declined faster than photosynthetic capacity.Abbreviations LNx leaf number x, counted in acropetal direction - DAP days after planting - DALA days after leaf appearance - Ci CO2 concentration in the leaf - Ca CO2 concentration in ambient air - LWP leaf water potential - OP osmotic potential - PAR photosynthetically active radiation  相似文献   

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