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。     

小麦拔节期淹水对叶片光合特性的影响

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CO2 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(9 d 之后), 净光合速率持续下降, 而叶片胞间CO2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。     

干旱胁迫对小麦幼苗根系生长和叶片光合作用的影响

采用水培试验方法,以2个耐旱性不同的小麦品种(敏感型望水白和耐旱型洛旱7号)为材料,研究了干旱胁迫对小麦幼苗根系形态、生理特性以及叶片光合作用的影响,以期揭示小麦幼苗对干旱胁迫的适应机制.结果表明： 干旱胁迫下,2个小麦品种幼苗的根系活力显著增大,而根数和根系表面积受到抑制;干旱胁迫降低了望水白的叶片相对含水量,提高了束缚水/自由水,而对洛旱7号无显著影响;干旱胁迫降低了2个小麦品种叶片的叶绿素含量、净光合速率、蒸腾速率、气孔导度和胞间CO2浓度,但随胁迫时间的延长,洛旱7号的叶绿素含量和净光合速率与对照差异不显著;干旱胁迫降低了2个小麦品种幼苗的单株叶面积,以及望水白的根系、地上部和植株生物量,而对洛旱7号无显著影响.水分胁迫下,耐旱型品种可以通过提高根系活力、保持较高的根系生长量来补偿根系吸收面积的下降,保持较高的根系吸水能力,进而维持较高的光合面积和光合速率,缓解干旱对生长的抑制.     

干旱胁迫对小麦幼苗根系生长和叶片光合作用的影响

采用水培试验方法,以2个耐旱性不同的小麦品种(敏感型望水白和耐旱型洛旱7号)为材料,研究了干旱胁迫对小麦幼苗根系形态、生理特性以及叶片光合作用的影响,以期揭示小麦幼苗对干旱胁迫的适应机制.结果表明： 干旱胁迫下,2个小麦品种幼苗的根系活力显著增大,而根数和根系表面积受到抑制;干旱胁迫降低了望水白的叶片相对含水量,提高了束缚水/自由水,而对洛旱7号无显著影响;干旱胁迫降低了2个小麦品种叶片的叶绿素含量、净光合速率、蒸腾速率、气孔导度和胞间CO2浓度,但随胁迫时间的延长,洛旱7号的叶绿素含量和净光合速率与对照差异不显著;干旱胁迫降低了2个小麦品种幼苗的单株叶面积,以及望水白的根系、地上部和植株生物量,而对洛旱7号无显著影响.水分胁迫下,耐旱型品种可以通过提高根系活力、保持较高的根系生长量来补偿根系吸收面积的下降,保持较高的根系吸水能力,进而维持较高的光合面积和光合速率,缓解干旱对生长的抑制.     

欧洲3种常见乔木幼苗在两种光环境下叶片的气体交换、叶绿素含量和氮素含量

在室内测定了分别栽培于全光照和20％光照条件下的垂枝桦Betulapendula,欧洲水青冈Fagussylvatica和欧洲白栎Quercusrobur幼苗叶片的光合作用－光响应曲线、叶片气孔导度、胞间二氧化碳浓度、水分利用效率,叶绿素含量和氮素含量,并分析叶片叶绿素含量和净光合速率的回归关系．20％光照条件引起净光合速率的光饱和点下降,叶片气孔导度和水分利用效率以及单位叶面积叶绿素含量降低,叶片的光合物质积累减少,但氮素含量上升．回归分析结果表明,叶片叶绿素含量与净光合速率成正相关．3种植物的幼苗对荫蔽条件有一定的适应性,其中B．pendula和Q．robur的耐荫能力比Fsylvatica强.     

BTH和SA处理及白粉菌接种对甜瓜叶片光合特性的影响

以抗病品种Tam Dew和感病品种卡拉克赛为材料,研究了BTH和SA处理及白粉菌接种对甜瓜叶片叶面积、叶绿素含量、净光合速率、气孔导度、胞间CO2浓度的影响.结果表明,BTH和SA处理及白粉菌接种对甜瓜苗期叶面积扩展无显著影响;BTH和SA处理植株的叶片(第3叶)和新生叶片(第5叶)的净光合速率、叶绿素含量和气孔导度显著高于对照;白粉菌接种后,2个甜瓜叶片的叶绿素含量、净光合速率和气孔导度显著降低,而BTH和SA处理能缓解由白粉菌接种带来的叶绿素含量、净光合速率和气孔导度的下降趋势.说明BTH和SA处理能延长甜瓜叶片的光合寿命,延缓甜瓜叶片的叶绿素含量、净光合速率和气孔导度的下降趋势.     

羊草和紫花苜蓿人工草地光合特性

为探究单播与混播人工草地对羊草和紫花苜蓿光合特性的影响,测定2种牧草光合特性日变化进程,比较不同处理下羊草和紫花苜蓿光合特征。结果表明：单播处理下,羊草和紫花苜蓿的净光合速率、蒸腾速率、叶片温度呈单峰型,紫花苜蓿的气孔导度呈单峰型,羊草的气孔导度和水分利用效率呈双峰型。混播处理下,羊草和紫花苜蓿的净光合速率、蒸腾速率、叶片温度日变化呈单峰型,羊草的气孔导度和水分利用效率呈单峰型,紫花苜蓿的气孔导度呈双峰型。混播处理下,羊草净光合速率峰值显著高于单播,分别为17.72和13.65μmol CO₂·m^-2·s^-1。单播和混播处理下,羊草叶绿素含量均高于紫花苜蓿,羊草叶片氮含量均低于紫花苜蓿,且混播羊草叶片氮含量显著高于单播羊草,二者分别为27.60和22.55 g·kg^-1。不同种植方式下,羊草和紫花苜蓿的净光合速率与气孔导度、蒸腾速率呈显著正相关,与胞间CO₂浓度呈显著负相关,紫花苜蓿的净光合速率与叶片温度、水分利用效率呈显著正相关。混播处理有利于增加羊草叶片氮含量。试验结果为牧...     

田间小麦叶片光合效率日变化与光合“午睡”的关系

小麦灌浆初期叶片(旗叶)晴天中午光合速率下降(“午睡”)伴随了气孔导度、胞间CO_2浓度下降,而气孔限制值中午升高,进一步证实气孑L中午关闭是光合“午睡”的一个重要原因。叶片光合效率的中午下降并非都伴随着光合“午睡”现象。当两者同时发生时,胞间CO_2浓度降低,而光合速率与气孔导度、胞间CO_2浓度之间的相关性高于光合速率与光合效率之间的相关性。这些事实表明。即使光合效率中午下降是光合“午睡”的部分原因,但较之气孔中午关闭只是一个次要原因。     

汞胁迫对白骨壤(Avicennia marina)幼苗生理生态的影响

为了解红树植物的重金属抗性机制,对白骨壤(Avicennia marina)幼苗进行不同浓度Hg2+(1、5、10、50、100 mg·L-1)的胁迫实验,测定并分析了Hg2+胁迫对白骨壤幼苗叶片的光合作用和抗氧化酶活性的影响.结果表明:叶片净光合速率随着胁迫时间的延长而降低,高浓度(≥150 mg·L-1)Hg2+胁迫下叶片的净光合速率低于中低浓度胁迫,且高浓度胁迫的叶片净光合速率在48 h后快速下降;叶片净光合速率与胞间二氧化碳浓度呈极显著负相关,叶绿素含量随Hg2+浓度的增加而降低.气孔导度在不同浓度胁迫下反应不同,低浓度Hg2+对白骨壤幼苗光合的影响可能是气孔因素,中高浓度Hg2+对白骨壤幼苗光合作用的抑制主要是非气孔因素.低浓度Hg2+胁迫,白骨壤幼苗叶片SOD、POD活性升高,表现了一定的抗逆性,而高浓度表现为抑制作用,基本在100 mg·L-1 Hg2+胁迫下活性达到最低值.说明Hg2+可以抑制白骨壤叶片的光合活性,高浓度Hg2+胁迫削弱了白骨壤的活性氧清除能力,植物极易受到伤害.     

不同浇水量对毛乌素沙地沙柳幼苗气体交换过程及其光化学效率的影响

 利用毛乌素沙地优势灌木沙柳(Salix psammophila)幼苗,研究气体交换及其PSⅡ的光化学效率对4种浇水量响应。结果表明：不同浇水量明显影响沙柳幼苗净光合速率、蒸腾速率、气孔导度、胞间CO2浓度和叶片温度日变化动态;除幼苗叶片温度随着浇水量的增加而降低外,其它以上因素均随浇水量的增加而增大。浇水量少时,幼苗净光合速率明显有“午睡”现象,而充足浇水能有效消除幼苗净光合速率的“午睡”现象;浇水量增加降低了沙柳幼苗光补偿点,提高了饱和光强和表观量子效率;浇水量显著影响幼苗的PSⅡ光化学效率,随着浇水量减少,幼苗的最大荧光、可变荧光、最大荧光比和最大光化学效率逐渐减小。相关分析反映了在不同施水量处理下,环境因子光合有效辐射、大气温度、大气饱和水汽压差及其生理变量气孔导度、叶片温度、胞间CO2浓度均显著影响幼苗净光合速率。     

Effect of Root Position on Measured Root Position on Measured Root Membrane Potentials

Root membrane potentials were measured by interposing a plantroot between two KCI solutions of different concentrations.The potentials measured across the two calomel electrodes werefound to depend on the position of the root. The potentialswere found to be lower when the root tip rather than the rootbase was in contact with the more concentrated solution. Thisindicates that the two parts of the root do not have the samein transport properties. Using an approximate theoretical treatmentthe observed potentials could be accounted for.     

Root decisions

Root systems have recognizable developmental plans when grown in solution or agar; however, these plans often must be modified to cope with the prevailing conditions in the soil environment such as the avoidance of obstacles and the exploitation of nutrient-rich patches or water zones. The modular structure of roots enables them to respond to their environment, and roots are very adaptive at modifying growth throughout the root system to concentrate their efforts in the areas that are the most profitable. Roots also form associations with microorganisms as a strategy to enhance resource capture. However, while the responses of roots in nutrient patches are well-recognized, overall 'rules of response' and variation in strategy among plant species that can be applied in a number of different environments are still lacking. Finally, there is increasing evidence that root–root interactions are much more sophisticated than previously thought, and the evidence for roots to identify self from non-self roots will be briefly discussed.     

Root Growth Inhibitors from Root Cap and Root Meristem of Zea mays L.

A micro-assay based on the growth inhibition of root segmentsof the seminal roots of Zea mays has been used to investigatethe root-growth-inhibiting substances in root caps and meristemsrespectively of the roots of Zea mays. This micro-assay is sensitiveto 50 pg of IAA or less. Paper chromatography of the acid fractionof methanolic extracts shows the presence of one main inhibitorin root caps and a different main inhibitor in root meristems.Neither is IAA, whose presence in meristems is sometimes indicatedby small inhibitions (or stimulations) at the characteristicRf of IAA. A Commelina leaf-epidermis assay shows the presenceof one stomata-closing ABA-like substance in root caps and onein meristems, one corresponding in Rf to the main root-growthinhibitor from the root cap. The implications of these findingsfor the geotropic responses of roots is briefly discussed.     

Root gravitropism

When a plant root is reoriented within the gravity field, it responds by initiating a curvature which eventually results in vertical growth. Gravity sensing occurs primarily in the root tip. It may involve amyloplast sedimentation in the columella cells of the root cap, or the detection of forces exerted by the mass of the protoplast on opposite sides of its cell wall. Gravisensing activates a signal transduction cascade which results in the asymmetric redistribution of auxin and apoplastic Ca²⁺ across the root tip, with accumulation at the bottom side. The resulting lateral asymmetry in Ca²⁺ and auxin concentration is probably transmitted to the elongation zone where differential cellular elongation occurs until the tip resumes vertical growth. The Cholodny-Went theory proposes that gravity-induced auxin redistribution across a gravistimulated plant organ is responsible for the gravitropic response. However, recent data indicate that the gravity-induced reorientation is more complex, involving both auxin gradient-dependent and auxin gradient-independent events.     

植物根的发育

介绍了目前通过模式植物拟南芥的研究,对胚胎时期胚根的起源、侧根的起源以及原后根的生长发育等问题一些有意义的研究成果,阐述了根结构与发育的控制机制,指出位置信息、静止中心、基因在根生长发育中的作用和影响。分析了根的结构与根端分生组织的关系。     

Root architecture

<正>Numerous research publications over the past 20 years have made it quite clear that a better understanding of the molecular and genetic basis for variation in root system architecture(RSA)will greatly aid the development of crop varieties with improved and more ef ficient nutrient and water acquisition under limiting conditions.In many parts of the world,especially in developing     

Root flavonoids

Informations on root flavonoids have been extensively reviewed and their functional diversity critically appraised. Root flavonoids play significant roles in protecting the plants against pests and diseases, regulating root growth and functions, influencing different aspects of nitrogen cycle and exerting allelopathic growth effects. They also constitute an essential source of Pharmaceuticals. An exhaustive list of flavonoids which are of significance in relation to these properties has been compiled. A thorough understanding of the flavonoid composition, level, metabolism and regulation in the roots of various plants may help us in developing several applied topics. Safe and specific chemicals against root pests; chemicals regulating root growth and mineral nutrition; plant varieties resistant to root pests and adverse allelopathic effects; an improved nitrogen economy in agroecosystems; desirable varieties of medicinal plants, in whose roots flavonoids are the active principles; in vitro systems for flavonoid production obtained from root cultures, at a commercial scale.