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In two experiments, the effect has been investigated of a mildand a more prolonged drought on the spatial distribution ofgrowth, epidermal cell lengths and cell wall peroxidase activitiesin the leaf elongation zone of the grass species Lolium temulentumL. In both experiments drought reduced the size of the elongationzone and local rates of elongation within it. Abrupt increasesin cell wall-associated peroxidase activity occurred at or closeto the position where elongation ceased in the leaf elongationzones of well-watered and mildly drought-stressed plants. Moreprolonged drought caused a 200–300% increase in the cellwallassociated peroxidase activity in the elongation zone only.The significant increase in the elongation zone cell wall peroxidaseactivity and its spatial variation provides evidence of a potentiallycausal role for cell wall-associated peroxidase in restrictingcell expansion during drought. Key words: Cell wall peroxidase, leaf expansion, drought  相似文献   

4.
Abstract Temporal analyses of cell division and tissue expansion in pea, tobacco, and sunflower leaves reveal that both processes follow similar patterns during leaf development. Relative cell division and relative tissue expansion rates are maximal and constant during early leaf development, but they decline later. In contrast, relative cell expansion rate follows a bell-shaped curve during leaf growth. Cell division and tissue expansion have common responses to temperature, intercepted radiation, and water deficit. As a consequence, final leaf area and cell number remain highly correlated throughout a large range of environmental conditions for these different plant species, indicating that cell division and tissue expansion are co-ordinated during leaf development. This co-ordination between processes has long been explained by dependence between both processes. Most studies on dicotyledonous leaf development indicate that leaf expansion rate depends on the number of cells in the leaf. We tested this hypothesis with a large range of environmental conditions and different plant species. Accordingly, we found a strong correlation between both absolute leaf expansion rate and leaf cell number. However, we showed that this relationship is not necessarily causal because it can be simulated by the hypothesis of independence between cell division and tissue expansion according to Green's theory of growth (1976). Received 23 February 2000; accepted 3 March 2000  相似文献   

5.
干旱对夏玉米苗期叶片权衡生长的影响   总被引:3,自引:0,他引:3  
麻雪艳  周广胜 《生态学报》2018,38(5):1758-1769
叶片是植物对干旱响应最敏感的器官之一,叶片性状变化及其权衡关系能够反映植物对资源的利用策略以及对干旱的适应对策。基于2014年6个初始土壤水分梯度的夏玉米持续干旱模拟试验研究表明,随着干旱的发展,夏玉米各叶片性状均会受到影响,但不同干旱程度的影响不一致。基于水分胁迫系数及干旱持续时间提出了干旱程度的定量表达,随着干旱的发生发展,干旱程度在0—1之间变化。当干旱程度小于0.21时,夏玉米叶片性状不会受到显著影响;0.21—0.76时,叶片性状大小受到影响,但变化趋势不会发生改变;0.76—0.91时,新叶形成补偿不了老叶脱落,有效叶片数、叶干重、绿叶面积和叶含水量等性状提前出现下降趋势;大于0.91时,叶片生长几乎停滞。夏玉米叶片性状在干旱条件下的适应性生长本质上体现了其在快速生长与维持生存之间的权衡,但不同干旱程度下,夏玉米叶片性状生长的权衡策略不同:未发生干旱时,夏玉米倾向于维持较高的代谢活性,一旦干旱程度大于0,夏玉米就会降低叶片代谢活性;当干旱程度小于0.48时,夏玉米倾向于通过迅速增加叶面积来吸收较多的能量,以获得较大的生长速率,为生殖器官的生长及产量形成储备能量;当干旱程度大于0.48时,夏玉米会减小单叶面积以减少水分散失,倾向于资源贮存以提高其生存能力。  相似文献   

6.
Despite the importance of understanding plant growth, the mechanisms underlying how plant and fruit growth declines during drought remain poorly understood. Specifically, it remains unresolved whether carbon or water factors are responsible for limiting growth as drought progresses. We examine questions regarding the relative importance of water and carbon to fruit growth depending on the water deficit level and the fruit growth stage by measuring fruit diameter, leaf photosynthesis, and a proxy of cell turgor in olive (Olea europaea). Flow cytometry was also applied to determine the fruit cell division stage. We found that photosynthesis and turgor were related to fruit growth; specifically, the relative importance of photosynthesis was higher during periods of more intense cell division, while turgor had higher relative importance in periods where cell division comes close to ceasing and fruit growth is dependent mainly on cell expansion. This pattern was found regardless of the water deficit level, although turgor and growth ceased at more similar values of leaf water potential than photosynthesis. Cell division occurred even when fruit growth seemed to stop under water deficit conditions, which likely helped fruits to grow disproportionately when trees were hydrated again, compensating for periods with low turgor. As a result, the final fruit size was not severely penalized. We conclude that carbon and water processes are able to explain fruit growth, with importance placed on the combination of cell division and expansion. However, the major limitation to growth is turgor, which adds evidence to the sink limitation hypothesis.  相似文献   

7.
Sensitivity of soybean leaf development to water deficits   总被引:4,自引:1,他引:3  
Abstract. Drought effects on the final leaf area of individual leaves were hypothesized to depend on the leaf developmental stage at which drought occurred. To evaluate this hypothesis, final leaf area and cell number were measured for soybean ( Glycine max (L.) Merr.) leaves that were at different stages of development when single or cyclical drought treatment was imposed. Leaf emergence rate from the meristem, as depicted by changes in the plastochron index, was not as sensitive as leaf expansion to cyclical droughts. For leaf expansion, small leaves, once they emerged from the meristem, suffered larger decreases in growth than leaves undergoing rapid leaf area expansion. Decreases in final leaf area as a result of a cyclical drought were correlated with decreases in final cell number. Decreases resulting from a single 8-d drought were dependent on the age of the leaf at the time of drought, because small leaves were found to have proportionately larger decreases in final cell number and area than larger leaves. These results indicated that age-dependent leaf responses to drought are based on the relative activity of cell division and expansion at the time stress was imposed.  相似文献   

8.
Drought responses of diurnal gas exchange, malic acid accumulation and water status were examined in Delosperma tradescantioides , a succulent that grows in drought-prone microenvironments in summer rainfall and all-year rainfall regions of southern Africa. When well-watered, this species exhibited Crassulacean acid metabolism (CAM)-cycling, but its carbon fixation pattern changed during the development of drought, shifting to either low-level CAM or to CAM-idling. The rate and pattern of this change depended on environmental conditions, duration of water stress and leaf age. At the onset of drought, diurnal malate fluctuation increased, but was strongly depressed (by ca 70%) as drought continued, and when leaf water content and water potential were low (ca 35 and 50% of the initial levels, respectively). When rewatered, rates of growth and photosynthesis, gas exchange and water status recovered fully to pre-stressed values within two days. Whole-shoot carbon uptake rates suggested that leaf growth had continued unabated during a short-term (≅ one week) drought. This emphasises that CAM-idling allows the maintenance of active metabolism with negligible gas exchange when soil water is limiting. It is possible that old or senescent leaves may provide water for the expansion of developing leaves during initial periods of drought. Regardless of the water regime and environmental conditions, leaf nocturnal malate accumulation and water content were positively correlated and increased with leaf age. Thus the gradual loss of water from older mature leaves may induce CAM-idling, which reduces water loss. An important ecological consequence of this combination of CAM modes is the potential to switch rapidly between fast growth via C3 gas exchanges when well-watered to water-conserving CAM-idling during drought.  相似文献   

9.
Drought responses of diurnal gas exchange, malic acid accumulation and water status were examined in Delosperma tradescantioides , a succulent that grows in drought-prone microenvironments in summer rainfall and all-year rainfall regions of southern Africa. When well-watered, this species exhibited Crassulacean acid metabolism (CAM)-cycling, but its carbon fixation pattern changed during the development of drought, shifting to either low-level CAM or to CAM-idling. The rate and pattern of this change depended on environmental conditions, duration of water stress and leaf age. At the onset of drought, diurnal malate fluctuation increased, but was strongly depressed (by ca 70%) as drought continued, and when leaf water content and water potential were low (ca 35 and 50% of the initial levels, respectively). When rewatered, rates of growth and photosynthesis, gas exchange and water status recovered fully to pre-stressed values within two days. Whole-shoot carbon uptake rates suggested that leaf growth had continued unabated during a short-term (∼ one week) drought. This emphasises that CAM-idling allows the maintenance of active metabolism with negligible gas exchange when soil water is limiting. It is possible that old or senescent leaves may provide water for the expansion of developing leaves during initial periods of drought. Regardless of the water regime and environmental conditions, leaf nocturnal malate accumulation and water content were positively correlated and increased with leaf age. Thus the gradual loss of water from older mature leaves may induce CAM-idling, which reduces water loss. An important ecological consequence of this combination of CAM modes is the potential to switch rapidly between fast growth via C3 gas exchanges when well-watered to water-conserving CAM-idling during drought.  相似文献   

10.
The effect of drought and recovery on cellular and spatial parametersof the growth process in tall fescue leaves was studied in twoexperiments. In both experiments plants grown on vermiculiteand maintained in a controlled environment were submitted toa 7 d drought period generated by withholding water. Droughtwas followed by a 3 d recovery period in experiment II. As leafelongation rate (LER) decreased during developing drought boththe growth zone length (initially 40 mm) and the maximum relativeelemental growth rate (initially 0.09 mm mm–1 h–1during the dark period of diurnal cycles) within the growthzone declined. But the growth zone still exhibited a lengthof approximately 15 mm when LER approached 0 under severe drought(–2.0 MPa predawn leaf water potential). The growth potentialof the basal 15-mm-long portion of the leaf was conserved duringthe period when drought effected the complete arrest of leafelongation. A (retrospective) analysis of the position-timerelationships of epidermal cells identified on leaf replicas(experiment II) indicated that the cell flux out of the growthzone responded very sensitively to drought. Before drought theflux was maximum at approximately 3.2 cells (cell file h)–1during the dark period. Flux decreased to 0 when leaf elongationstopped. Flux also varied diurnally both under well-wateredand droughted conditions. In well-watered conditions it wasabout 30% less during the light than the dark period. Cell elongationwas also sensitive to drought. Under well-watered conditionsepidermal cell elongation stopped when cells attained a lengthof approximately 480 µm. During developing drought cellsstopped elongating at progressively shorter lengths. When LERhad decreased to almost nil, cells stopped elongating at a lengthof approximately 250 µn. When drought was relieved followinga 2 d complete arrest of leaf elongation then cells shorterthan 250 µm were able to resume expansion. Following rewateringcell flux out of the growth zone increased rapidly to and abovethe pre-drought level, but there was only a slow increase overtime in the length at which cell elongation stopped. About 2d elapsed until the leaf growth zone produced cells of similarlength as before drought (i.e. approximately 480 µm). Key words: Epidermal cell length, cell flux, (leaf) growth zone, leaf elongation rate, relative elemental growth rate, position-time relationships (path line, growth trajectory), drought, water deficit  相似文献   

11.
We report that phytochrome B (phyB) mutants exhibit improved drought tolerance compared to wild type (WT) rice (Oryza sativa L. cv. Nipponbare). To understand the underlying mechanism by which phyB regulates drought tolerance, we analyzed root growth and water loss from the leaves of phyB mutants. The root system showed no significant difference between the phyB mutants and WT, suggesting that improved drought tolerance has little relation to root growth. However, phyB mutants exhibited reduced total leaf area per plant, which was probably due to a reduction in the total number of cells per leaf caused by enhanced expression of Orysa;KRP1 and Orysa;KRP4 (encoding inhibitors of cyclin-dependent kinase complex activity) in the phyB mutants. In addition, the developed leaves of phyB mutants displayed larger epidermal cells than WT leaves, resulting in reduced stomatal density. phyB deficiency promoted the expression of both putative ERECTA family genes and EXPANSIN family genes involved in cell expansion in leaves, thus causing greater epidermal cell expansion in the phyB mutants. Reduced stomatal density resulted in reduced transpiration per unit leaf area in the phyB mutants. Considering all these findings, we propose that phyB deficiency causes both reduced total leaf area and reduced transpiration per unit leaf area, which explains the reduced water loss and improved drought tolerance of phyB mutants.  相似文献   

12.
The effects of senescence and drought on the levels and activities of chlorophyllase (EC 3.1.1.14), phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) and ribulose-1,5-bisphosphate carboxylase (Rubisco, EC 4.1.1.39) in the intact primary leaves of soybean ( Glycine max L. cv. Jackson) were monitored. Plants were grown either (1) for 2 to 8 weeks and the primary leaves harvested every week or (2) for 2 weeks and the plants subjected to drought stress and compared to control plants that were watered daily. In the senescence experiment, chlorophyllase activity changed in parallel with water content, leaf chlorophyll and total protein per unit dry weight of leaf tissue, with all factors increasing in concert during expansion of the primary leaves in the first 4 to 5 weeks of seedling development. Thereafter, all factors, including chlorophyllase activity, declined reaching markedly reduced values at weeks 7 and 8 when the primary leaves were yellow and ready to abscise. PEPC and Rubisco activities peaked in the third week, i.e. well before full leaf expansion, and then declined. In contrast to its response during senescence, chlorophyllase activity per unit leaf dry weight did not change during drought stress, but the specific activity of the enzyme rose and showed an inverse relationship to total leaf chlorophyll and protein content. Rubisco activity was highly sensitive to drought, with decrements observed in the activity and in levels of the large subunit within 2 days of withholding water and before significant changes in leaf water content were detected.  相似文献   

13.
We have followed the expansion of individual pea leaves frominitiation to maximum area, over two markedly different periods.During the first one (2/3 of total leaf development time), cellproduction occurred while cell and leaf expansions were slow.Rapid expansion (95% of total) occurred for a second periodlasting 1/3 of total development time, whereas cell divisionwas virtually completed. Water deficits of 15 d were appliedduring either slow or rapid expansion, and characterized bymeasurements of soil water potential, stomatal conductance,leaf water potential and xylem [ABA]. Plants which experiencedwater deficit during the slow expansion period had markedlyreduced expansion during the second period (i.e. 1 or 2 weeksafter cessation of deficit), while all variables characterizingwater status were returned to the level of the control. This‘after effect’ was accounted for by a reduced cellnumber per leaf, while individual cell area was not affected.In contrast, water deficit occurring during rapid leaf expansionimmediately reduced leaf expansion via cell area, without affectingcell number per leaf. These experiments indicate a role, inthe response to water deficits, for events occurring very earlyin the development of pea leaves, while leaf expansion is tooslow to be measured with macroscopic methods. This role wouldbe accounted for by cell production during the first 2/3 ofleaf development while cell expansion would account for changesin the area of leaves experiencing a later stress. These resultssuggest that long-term temporal analysis may be essential inthe study of dicot leaf expansion compared to monocot leaveswhere temporal analysis can be inferred from spatial analysis. Key words: Leaf growth, dicot leaves, water stress, ell division, cell expansion, Pisum sativum L.  相似文献   

14.
马铃薯块茎膨大期不同程度干旱后复水的源库补偿效应   总被引:1,自引:0,他引:1  
旱后复水的补偿效应在多种作物的不同生育时期都存在,是植物抵抗逆境胁迫和伤害的重要自我调节机制,也是对有限水分高效利用的体现.本研究在马铃薯块茎膨大期进行两轮干旱后复水处理,明确马铃薯补偿效应产生的干旱胁迫阈值,并从源-库角度探索马铃薯旱后复水补偿效应产生的缘由.试验选取‘大西洋’马铃薯脱毒组培苗为材料,设置充分供水(W)、轻度干旱后复水(D1-W)、中度干旱后复水(D2-W)和重度干旱后复水(D3-W)4个水分处理并经过两个循环.结果表明:在经过两轮轻度干旱复水后,马铃薯产量表现出超补偿效应,水分利用效率和产量比充分供水分别提高了17.5%和6.3%;中度水分胁迫表现出近等量补偿效应,产量与充分供水差异不大,而水分利用效率提高了8.4%;而重度水分胁迫没有表现出产量补偿效应.不同程度的干旱胁迫均降低马铃薯叶片叶绿素含量、净光合速率、叶面积等源的大小和活性,而在复水后,轻度和中度胁迫出现了超补偿和补偿效应,增强了源的供应能力.同时,适度干旱后复水显著增强了块茎(库)中蔗糖-淀粉代谢途径关键酶的活性,提高了库活性,进而表现为块茎平均重量的增加.综上,马铃薯块茎膨大期适度的水分亏缺在复水后源-库均存在补偿和超补偿效应,以此来弥补干旱带来的损失,最终在产量上表现为补偿或者超补偿效应,并显著提高了水分利用效率.  相似文献   

15.
The tropical rainforest mesocosm within the Biosphere 2 Laboratory, a model system of some 110 species developed over 12 years under controlled environmental conditions, has been subjected to a series of comparable drought experiments during 2000–2002. In each study, the mesocosm was subjected to a 4–6 week drought, with well‐defined rainfall events before and after the treatment. Ecosystem CO2 uptake rate (Aeco) declined 32% in response to the drought, with changes occurring within days and being reversible within weeks, even though the deeper soil layers did not become significantly drier and leaf‐level water status of most large trees was not greatly affected. The reduced Aeco during the drought reflected both morphological and physiological responses. It is estimated that the drought‐induced 32% reduction of Aeco has three principal components: (1) leaf fall increased two‐fold whereas leaf expansion growth of some canopy dominants declined to 60%, leading to a 10% decrease in foliage coverage of the canopy. This might be the main reason for the persistent reduction of Aeco after rewatering. (2) The maximum photosynthetic electron transport rate at high light intensities in remaining leaves was reduced to 71% for three of the four species measured, even though no chronic photo‐inhibition occurred. (3) Stomata closed, leading to a reduced ecosystem water conductance to water vapour (33% of pre‐drought values), which not only reduced ecosystem carbon uptake rate, but may also have implications for water and energy budgets of tropical ecosystems. Additionally, individual rainforest trees responded differently, expressing different levels of stress and stress avoiding mechanisms. This functional diversity renders the individual response heterogeneous and has fundamental implications to scale leaf level responses to ecosystem dynamics.  相似文献   

16.
Carbon isotope discrimination (Δ) was measured in irrigated and droughted potato. Under irrigation, Δ in leaflets at given nodes increased (P < 0.001) between 21 and 63 d after emergence (DAE), which was attributed to increasing stomatal conductance (gs) during leaf expansion. The effect of leaf position on Δ was non-significant in mature leaves. Under drought, Δ decreased (P < 0.001) in successive leaves up the stem, reflecting changes in gs and water stress. At each node Δ remained constant or decreased, suggesting that effects of water stress were greater than changes with leaf expansion. There were significant differences in Δ between cultivars in both treatments, and in the progressive decrease in Δ up the stem under drought. Differences in Δ between cultivars were consistent with differences in stomatal control of leaf water status following water stress. Values for Δ in tubers were consistently lower than in stem and leaf, and decreased more rapidly. Differences in Δ between cultivars did not reflect dry matter production in either treatment, and differences in water use were non-significant between cultivars under drought. So, plants can achieve similar dry matter production through different growth strategies when irrigated or droughted, and Δ does not provide a simple, indirect method of selecting for dry matter production under water stress.  相似文献   

17.
Genetic variability in the plasticity of leaf area expansion in response to water deficit has been reported in Arabidopsis thaliana. Here, the objective was to identify the underlying dynamic and cellular processes involved in this variability. Twenty-five accessions were subjected to identical soil water deficit treatments. In all accessions, the plasticity of leaf production was low compared with that of individual leaf expansion. A subset of accessions was selected for further dissection of individual leaf expansion into its underlying variables: the rate and duration of leaf expansion and epidermal cell number and area. In all accessions, water deficit had opposite effects on the rate and duration of leaf expansion. The accumulation of these effects was reflected in changes in final leaf area. At the cellular level, moderate water deficits had opposite effects on cell number and cell size, but more severe ones reduced both variables. The importance of these opposing effects is highlighted by the behaviour of the accession An-1, for which the compensation between the decrease in leaf expansion rate and the increase in the duration of expansion is total. This dynamic plasticity in response to water deficit is not detectable when only final measurements are done.  相似文献   

18.
Water relations of cotton flower petals and fruit   总被引:5,自引:2,他引:3  
Water needed for expansion is believed to enter plant tissue in response to a growth-induced water potential gradient that occurs as turgor is reduced during relaxation of cell walls or in response to increased solutes. Under water stress, the cotton flower petal continues to expand when all leaves on the plant are wilted and new leaf expansion has ceased in the shoot tips. This study was undertaken to determine if water for expansion entered the petal in response to a gradient or to increased solutes. Water potentials of cotton petal, leaf, bract and fruit were determined pre-dawn and midday in dryland and irrigated field plots. The mechanism by which petal expansion occurs appears not to be associated with a growth-induced water potential gradient or to increased solutes because the gradient is reversed from that needed to drive expansion. The water potential of the petal tissues was consistently higher than that of the subtending leaves and bracts both during and after anthesis, and under different water stress conditions. How this reversal in water potential gradient is established and maintained should provide insight into mechanisms involved in growth during water stress.  相似文献   

19.
赵福年  张强  周广胜  王润元  陈斐  齐月  张凯  王鹤龄 《生态学报》2023,43(13):5581-5591
与缓慢发展的干旱过程不同,骤旱具有发生速度快,短期内可致害的特点。目前,关于作物骤旱致害的临界阈值及其调控机制尚不清楚。以春小麦为供试作物,通过桶栽试验,模拟研究骤旱过程中小麦受旱致害的过程特征及其控制因素。结果发现,发生骤旱时土壤含水量下降呈先快后慢的变化趋势,叶片水分和叶水势则呈先慢后快的指数变化趋势。叶片光合生理指标对土壤水分的下降存在明显的阈值响应,且不同生理指标的阈值并不完全相同,其中净光合速率与表征叶片光合能力的指标(最大羧化速率)对土壤有效含水量的响应阈值为0.4,气孔导度和蒸腾速率对土壤有效含水量的响应阈值分别为0.5和0.4。而小麦光合生理指标对叶片水分和叶水势的阈值响应并不明显。同时依据各生理指标相关和通径分析结果得出,骤旱发生时引起小麦叶片净光合速率快速降低的主导因子为非气孔因素,而并不是以往作物受旱研究中的气孔因素。本研究结果有望丰富干旱影响认知,并可为科学应对干旱提供依据。  相似文献   

20.
植物根系和叶片生长对水分亏缺的原初反应   总被引:14,自引:0,他引:14  
细胞扩张生长是植物受水分亏缺影响最敏感的生理过程之一。主要在对细胞水分导性、细胞壁特性和延伸组织中溶质传输结果分析的基础上 ,从细胞、组织和器官水平上对细胞扩展生长进行了探讨。根系和叶片细胞主要通过以下 2个过程来补偿水分胁迫的作用 :调节扩展生长需要的细胞临界膨压 ;溶质在延伸组织中的运移。此外 ,还探讨了植物根系和叶片生长对水分亏缺的生理适应机制  相似文献   

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