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1.
以‘拉丁诺’白三叶为材料,用0、10%、15%、20%(W/V)即的聚乙二醇(PEG-6000)溶液模拟干旱条件,研究亚精胺fSpd)浸种对渗透胁迫下白三叶种子萌发和淀粉代谢的影响。结果表明,在PEG渗透胁迫下,白三叶种子的发芽率、发芽势、发芽指数、胚芽及胚根鲜重和胚根长度均显著(P〈0.05)降低,淀粉水解为糖类的速率减慢;与蒸馏水浸种相比,0.05mmol.L-1 Spd浸种处理显著(P〈0.05)提高了在渗透胁迫条件下种子的发芽率、发芽势、发芽指数、胚芽及胚根鲜重、干重和胚根长度,同时大幅提高了α-淀粉酶、β-淀粉酶及(α+β).淀粉酶总活性,降低了淀粉含量,增加了还原糖和葡萄糖含量。说明Spd浸种提高了白三叶种子在渗透胁迫下的萌发能力和幼苗生长的环境适应性,这可能与增强种子体内淀粉酶活性,加速淀粉水解为还原糖和葡萄糖,为种子萌发和幼苗早期生长及时提供充足能量有关。  相似文献   

2.
洋葱种子含水量与贮藏温度对其寿命的影响   总被引:14,自引:0,他引:14  
不同含水量(MC 7.1%-1.2)的洋葱种子贮藏在35℃、室温、15℃和5℃条件下1-3年,适度超于处理能延长种子的贮藏寿命;种子的贮藏寿命与种子含水量和贮藏温度密切相关。种子贮藏的最适含水量随温度的改变而发生相应的变化,35℃时MC为3.4%;室温时为3.4%-3.5%;15℃时为4.5%-5.1%。MC≤2.2%不利于延长种子寿命。在室温自然条件下贮藏1-3年,适度超干种子(MC3.4%)内MDA和H2O2含量、O2^-产生速率和LOX活性明显地低于未超干种子(MC7.1%)和高度超干种子(MC1.2%),而抗氧化酶AsA-POD 、CAT和SOD的活性显著地高于未超干种子(MC7.1%)和高度超干种子(MC1.2%)。据此认为对脂质过氧化的抑制作用是适度超干种子耐贮藏的生理原因之一。  相似文献   

3.
矮沙冬青种子特性和萌发影响因素的研究   总被引:28,自引:0,他引:28       下载免费PDF全文
 对矮沙冬青(Ammopiptanthus nanus)种子的特性和萌发影响因素进行了初步研究,结果表明:种子不易传播;虫蛀率高,室温贮藏60 d的种子虫害率为38%;易形成硬实,含水量为7.68%的种子在30 ℃温水中浸泡90 h,只有33.33%能吸水膨胀。种子萌发时不需光,在15~30 ℃和室温(18~32 ℃)条件下,经9 d的萌发,发芽率均可达80%以上,30℃时萌发最快;在1~2 cm深的沙壤中,种子出苗率可达75%以上,超过3 cm显著降低,超过6 cm则低于20%;种子在沙壤中萌发时,沙壤的适宜湿度为19.35%~28.75%,高于32.43%或低于3.85%,很少有种子萌发;含水量分别为19.36%、10.64% 和7.68%的种子发芽率无显著差异,在-10 ℃和5 ℃下贮藏7个月,发芽率也无显著降低,但在室温和35 ℃下贮藏7个月则显著下降,发芽率下降的速度与种子本身的含水量和贮藏温度正相关;在湿度分别为7.41%、13.79%和28.57%的沙壤中播种育苗,幼苗死亡率高达77.49%、81.25%和89.49%,即使用三唑酮拌种,死亡率亦高达50.27%、69.53%和76.03%,幼苗死亡率与沙壤湿度正相关。  相似文献   

4.
为测定不同脱水程度金丝李(Garcinia paucinervis)种子的萌发情况及其复水后的吸水率、脱水过程中抗性生理指标的变化以及不同贮藏方式下种子的萌发情况,该文研究了金丝李种子的脱水敏感性和储藏特性。结果表明:(1)金丝李种子初始含水量为45.29%,室内通风处放置35 d失水率即达45%。(2)种子失水率低于18%时,萌发率和复水后的吸水率变化不显著;失水率超过18%时,萌发率和复水后吸水率均显著下降,失水率为42%时萌发率为0。其种子的临界含水量为27.29%,半致死含水量为12.72%。(3)随着种子脱水程度的加深,相对电导率、可溶性糖及脯氨酸含量逐步上升;丙二醛含量在失水率低于24%时变化不大,高于24%时显著提高; SOD和POD的活性均呈波动性变化,失水率为18%时活性均最高。(4)室温干藏1个月和-1、-20℃下湿藏1个月的种子均不能萌发;水浸贮藏1个月的种子萌发率显著降低; 4℃湿藏1、3和6个月均显著延缓种子萌发,但对萌发率无显著影响。表明金丝李种子在失水率低于18%时,种子可通过抗性调节维持细胞的正常代谢,能忍受一定程度的脱水和低温;当失水率超过18%时,种子代谢失衡发生劣变直至死亡,属于低度的顽拗性种子。4℃湿沙藏(含水量7.5%)是短期贮藏其种子的较好方法。  相似文献   

5.
用10、50、100、150和200mg·L-15种浓度赤霉素(GA3)溶液处理于10℃冰箱中贮藏5年的花椰菜老化种子。结果表明,100mg·L-1GA3浸种22h的效果最佳,老化种子的发芽率、发芽势、活力指数、根长均有提高,畸形苗率下降;过氧化物酶(POD)、过氧化氢酶(CAT)和脱氢酶活性提高,可溶性蛋白和叶绿素含量也提高,种子浸出液的电导率和丙二醛(MDA)含量则下降。另外,100mg·L-1GA3处理后的种子在温度为25℃条件下贮藏时间不宜超过25d。  相似文献   

6.
以沙芥种子(含水量4.5%)和斧形沙芥种子(含水量4.3%)为材料,采用硅胶干燥法将其含水量分别降至3.1%、2.2%、1.3%,在50℃、35℃和20℃条件下密闭贮藏1年,研究贮藏温度和超干处理对种子萌发指标、解剖结构的影响,为种子老化及贮藏研究提供理论参考。结果表明:(1)随着贮藏温度升高和种子含水量降低,沙芥和斧形沙芥种子的发芽率、胚根长、胚根干质量均在下降。(2)解剖观察发现,贮藏温度升高和种子含水量降低,首先加剧种子胚内部维管束组织活性的降低,其次由里及外对薄壁细胞活性和结构产生破坏,同时胚淀粉粒活性和数量下降。(3)沙芥和斧形沙芥种子分别在含水量4.5%和4.3%(CK)、并于20℃~35℃条件下贮藏后,种子的萌发和结构活性保持最好,而且斧形沙芥种子的保持能力强于沙芥。  相似文献   

7.
为探讨将种子发芽率转化为存活比,促使种子存活曲线转变成直线,并用于预测种子寿命的可行性,3个含水量水平的3种8个种子批的小麦种子被贮藏在20℃、30℃和40℃的温度下长达810d,以获取发芽率数据。比较和分析了概率、存活比与贮藏时间绘制的种子存活曲线、构建的概率回归和存活比线性回归方程的拟合性比,以及贮藏温度和种子含水量对种子死亡时间分布标准差的影响。结果表明,和概率值相比,存活比更容易使种子存活曲线直线化,和贮藏时间的线性回归方程的拟合性也更优于概率回归方程;贮藏温度和种子含水量的交互作用对种子寿命的影响是真实的,其作用也大于单独的温度、水分或水分的对数;只包含贮藏温度和种子含水量交互作用的预测种子寿命的存活比线性回归方程,即Gi/G0=A-P/10KE-CWH(t譵),被贮藏在低温种质库的小麦种子的实际发芽率和贮藏时间证明,是适合用于预测贮藏在低温种质库的小麦种子寿命的,尤其在预测发芽率时较预测贮藏时间有更高的准确性。  相似文献   

8.
测定水稻、玉米和狼见草花粉在低温(5℃)低湿(45%)、低温(5℃)高湿(80%)、高温(35℃)低湿(45%)和高温(35℃)高湿(90%)4种贮藏条件下的活力表明:低温高湿下花粉活力保持的时间最长;狼尾草花粉比水稻、玉米花粉耐贮藏,在低温高湿条件下贮藏30d后,仍有38.3%的萌发率;狼尾草花粉中蛋白质含量较高,淀粉含量较低。  相似文献   

9.
洋葱种子含水量与贮藏温度对其寿命的影响   总被引:2,自引:0,他引:2  
不同含水量(MC7.1%~1.2%)的洋葱种子贮藏在35℃、室温、15℃和5℃条件下1~3年,适度超干处理能延长种子的贮藏寿命;种子的贮藏寿命与种子含水量和贮藏温度密切相关。种子贮藏的最适含水量随温度的改变而发生相应的变化,35℃时MC为3.4%;室温时为3.4%~4.5%;15℃时为4.5%~5.1%。MC≤2.2%不利于延长种子寿命。在室温自然条件下贮藏1~3年,适度超干种子(MC3.4%)内MDA和H2O2含量、O-*2产生速率和LOX活性明显地低于未超干种子(MC7.1%)和高度超干种子(MC1.2%),而抗氧化酶AsA-POD、CAT和SOD的活性显著地高于未超干种子(MC7.1%)和高度超干种子(MC1.2%)。据此认为对脂质过氧化的抑制作用是适度超干种子耐贮藏的生理原因之一。  相似文献   

10.
紫花苜蓿种子对逆境贮藏条件的反应   总被引:7,自引:0,他引:7  
以陇东紫花苜蓿 (MedicagosativaL .cv .“Longdong”)种子为材料 ,在室温、35℃和 35℃ +10 %的种子含水量 (SMC) 3种贮藏、接种或不接种燕麦镰刀菌 (Fusariumavenaceum (Fr.)Sacc .)的条件下 ,1年贮藏期内对各逆境处理的种子每隔 6 0d进行 1次标准发芽试验 ,2 0℃恒温、第 10d统计种子的发芽率和死亡率 ,试验结束时计测种子幼苗的长度和感病率 ;在大田条件下观测各处理种子的出苗率 ,确定催腐 (CD)与各种贮藏条件下的苜蓿种带真菌种类和检出率 .结果表明 ,随着贮藏温度和种子含水量等逆境贮藏条件胁迫的加剧 ,苜蓿种带真菌检出率逐渐增高 ,从室温、35℃条件下的 10 %上升到CD +35℃ +10 %SMC条件下的 2 9% ;抗病性逐渐减弱 ,35℃ +10 %SMC条件下幼苗的感病率和种子死亡率显著 (P <0 .0 5 )高于室温和 35℃下的感病率和种子死亡率 ;室内种子发芽率和田间出苗率逐渐下降 ,35℃ +10 %SMC条件下的种子的发芽率和田间出苗率显著 (P <0 .0 5 )低于在室温和 35℃下的发芽率和田间出苗率 ;幼苗生长受到抑制 ,35℃ +10 %SMC条件下的苗长和根长显著 (P <0 .0 5 )低于在室温和 35℃下的幼苗长度 .随着贮藏时间的延长 ,种子真菌检出率和田间出苗率下降 ,幼苗感病率增加 .与未接种的对照相比 ,接种燕麦镰刀菌的种子  相似文献   

11.
A study was conducted to investigate the physiological responses of greenhouse-produced Oxalis corniculata seeds to light, temperature, moist heat treatment, aging, and season of production. Fresh seeds exhibited over 90% germination and required low levels of light (5 μmol m-2 s-1, 400–700 nm) to germinate. Seeds germinated over a broad, yet seasonally-dependent range of incubation temperatures. Seeds produced in winter had the narrowest temperature range of germination (15 to 25 C) and the lowest germination percent (44% at 2 wk) at optimum temperature (17 C); seeds produced in summer had the widest temperature range of germination (10 to 30 C) and the highest germination percent (93% at 2 wk) at optimum temperature (17 C). Incubation at non-optimum temperatures between 5 and 40 C suppressed or slowed the rate of germination until seeds were placed at optimum temperature, where full germination subsequently occurred. Moist heat treatment at temperatures over 40 C resulted in varying degrees of inhibition of subsequent germination. When seeds were stored dry in laboratory conditions, three of four seed lots examined retained over 80% germination capacity until ca. 8 months; 50% capacity remained after ca. 15 months. These results indicate that the seasonal temperature and daylength effects on maternal plants in the greenhouse environment are major determinants of seed germination characteristics of O. corniculata.  相似文献   

12.
BACKGROUND AND AIMS: Although a claim has been made that dormancy cycling occurs in seeds of Ipomoea lacunosa (Convolvulaceae) with physical dormancy, this would seem to be impossible since the water gap cannot be closed again after it opens (dormancy break). On the other hand, changes in sensitivity (sensitive <--> non-sensitive) to dormancy-breaking factors have been reported in seeds of Fabaceae with physical dormancy. The primary aim of the present study was to determine if sensitivity cycling also occurs in physically dormant seeds of I. lacunosa. METHODS: Treatments simulating conditions in the natural habitat of I. lacunosa were used to break seed dormancy. Storage of seeds at temperatures simulating those in spring, summer, autumn and winter were tested for their effect on sensitivity change. Seeds made non-dormant were stored dry in different temperature regimes to test for dormancy cycling. In addition, seeds collected on different dates (i.e. matured under different climatic conditions) were used to test for maternal effects on sensitivity to dormancy-breaking factors. KEY RESULTS: Sensitivity was induced by storing seeds under wet conditions and reversed by storing them under dry conditions at low (< or = 5 degrees C) or high (> or = 30 degrees C) temperatures, demonstrating that seeds of I. lacunosa can cycle between sensitive and insensitive states. Sensitive seeds required > or = 2 h at 35 degrees C on moist sand for release of dormancy. However, there is no evidence to support dormancy cycling per se. Conceptual models are proposed for sensitivity cycling and germination phenology of I. lacunosa in the field. CONCLUSIONS: Seasonal germination behaviour of physically dormant I. lacunosa seeds can be explained by sensitivity cycling but not by dormancy cycling per se. Convolvulaceae is only the second of 16 families known to contain species with physical dormancy for which sensitivity cycling has been demonstrated.  相似文献   

13.
白沙蒿种子萌发特性的研究 II. 环境因素的影响   总被引:9,自引:0,他引:9       下载免费PDF全文
白沙蒿(Artemisia sphaerocephala Kraseh.)是中国西北部沙漠的流动及固定沙丘上广泛分布的优势种灌木。白沙蒿种子为需光种子,种子在光下萌发而在黑暗中受到抑制。种子萌发的适宜温度为25℃,在10℃和30℃萌发速率和萌发率都很低,萌发在5℃受到抑制。种子在沙中被埋越深,其萌发速率和萌发率就越低。在沙平面下2cm或更深层沙土下出苗率为零。但是,当将种子上层沙土移走,只保留0.5cm沙土覆盖种子,这些种子的萌发率达到原先就位于沙土下0.5cm的种子的萌发率,但是后者的萌发速率较高。土壤水分含量越高,从1.7%到14.7%,其萌发就越快。土壤水分含量从19.4%起,种子的萌发受到了延迟,苗的发育受到了抑制.  相似文献   

14.
六盘山区辽东栎的实生苗更新及其影响因子   总被引:3,自引:2,他引:1       下载免费PDF全文
 研究了六盘山区辽东栎(Quercus liaotungensis)灌丛的种子产量、土壤种子库组成、湿沙和风干贮藏对种子寿命的影响以及动物取食子叶对种子萌发和幼苗建立的影响。结果表明, 辽东栎灌丛种子的完好率为27.51%, 被动物取食或搬运种子的比例(41.51%)显著高于其他类型种子(p < 0.01); 辽东栎次生林土壤种子库中萌发和虫蛀种子分别占35.16%和38.29%, 完好种子仅占13.65%, 捕食动物主要通过贮藏或搬运而影响土壤种子库中的种子密度。湿沙贮藏60天的辽东栎种子自动萌发率高达96.67%, 短期贮藏可加快种子的萌发进程, 提高萌发率和萌发指数, 但随着贮藏时间的延长, 种子萌发进程延迟, 萌发率、萌发指数和活力指数均不同程度地降低。排除动物取食处理的幼苗在林窗和林下生境的存活率分别为80%和83%, 而不排除动物取食幼苗在2种生境中分别仅有25%和31%能够存活, 表明子叶在幼苗建立中具有重要作用。林窗中幼苗子叶的动物取食率(85.00%)高于林下(71.00%), 子叶留存的幼苗在林窗中的存活率(6.00%)低于林下(15.50%), 而子叶被取食幼苗的存活率在两种环境中基本相等(分别为18.50%和18.00%)。  相似文献   

15.
Adenosine 3′,5′-cyclic monophosphate (cAMP) is known as a key second messenger in many living organisms, regulating a wide range of cellular responses. In higher plants the function of cAMP is poorly understood. In this study, we examined the role of cAMP in seed germination of the root parasitic plant Orobanche minor whose seeds require preincubation in warm moist environments for several days, termed conditioning, prior to exposure to germination stimulants released from roots of host plants. Accumulation of endogenous cAMP was observed in the conditioned O. minor seeds. When the seeds were exposed to light or supraoptimal temperature during the conditioning period, cAMP did not accumulate and the seeds showed low germination rates after stimulation with strigol, a germination stimulant. Addition of membrane-permeable cAMP to the medium restored the germination rates of the seeds treated with light or supraoptimal temperature during the conditioning period, suggesting that cAMP functions during the conditioning period. The endogenous cAMP levels of the seeds conditioned in the light or at a supraoptimal temperature were elevated by treatment of the seeds with gibberellin (GA) during the conditioning period. Uniconazole, a potent inhibitor of GA biosynthesis, blocked elevation of the cAMP level. Furthermore, a correlation between the endogenous cAMP level and GA level was observed during the conditioning period. These results suggest that GAs elevate the cAMP level, which is required for the germination of O. minor seeds.  相似文献   

16.
  • Information on the optimal conditions to promote the germination of Lamprocapnos spectabilis (L.) Fukuhara seeds is limited; consequently, this study was conducted to establish the requirements to break seed dormancy and promote germination.
  • The selected seeds had morphophysiological dormancy and had not begun embryo development. To study the dormancy breaking and embryo development processes, seeds were subjected to constant or changing temperature treatments during moist stratification.
  • High temperature and humidity resulted in vigorous embryo growth, with the longest embryos occurring after 1 month of incubation at 20 °C. At 4 °C, the seeds required incubation period of at least 3 months to germinate. Embryo growth and germination were higher with changing high and low temperatures than under a constant temperature, and changing temperatures also considerably changed the endogenous hormone levels, embryo development and germination. Bioactive gibberellin (GA) content was higher in seeds incubated at 20 °C for 1 month, then at 4 °C for 2 months. The content of endogenous abscisic acid in seeds subjected to the same treatment decreased by 97.6% compared with that of the untreated seeds.
  • Embryo growth and seed germination require changing high and low temperatures; however, exogenous GA3 could substitute for high temperatures, as it also causes accelerated germination. In this study, the seeds of L. spectabilis were identified as an intermediate simple type, a sub‐level of morphophysiologically dormant seeds.
  相似文献   

17.
The germination characteristics of a population of the winter annual Phacelia dubia (L.) Trel. var. dubia from the middle Tennessee cedar glades were investigated in an attempt to define the factor(s) regulating germination in nature. Factors considered were changes in physiological response of the seeds (after-ripening), temperature, age, light and darkness, and soil moisture. At seed dispersal (late May to early June), approximately 50 % of the seeds were non-dormant but, would germinate only at low temperatures (10–15 C). As the seeds aged from June to September, there was an increase in rate and total percent of germination at 10, 15, and 20 C, and the maximum temperature for germination increased to 25 C. Little or no germination occurred at the June, July, and August temperatures in 0- to 2-month-old seeds, even in seeds on soil that was kept continuously moist during this 3-month period. At the September, October, and November temperatures 3- to 5-month-old seeds germinated to high percentages. In all experiments seeds germinated better at a 14-hr photoperiod than in constant darkness. Inability of 0- to 2-month-old seeds to germinate at high summer temperatures allows P. dubia dubia to pass the dry summer in the seed stage, while increase in optimum and maximum temperatures for germination during the summer permits seeds to germinate in late summer and early fall when conditions are favorable for seedling survival and eventual maturation.  相似文献   

18.
In arid zones, precipitation distribution is extremely uneven, with saline‐waterlogging and dry–moist cycles appearing frequently, which negatively impact on seed germination and seedling establishment. The responses of two halophytes, Suaeda physophora and Haloxylon ammodendron, and a xerophyte, Haloxylon persicum, to saline‐waterlogging and dry–moist cycles were studied. The results showed that aeration increased seed germination for all species when seeds were submerged in NaCl, especially for xerophyte. Compared with S. physophora and H. ammodendron, seed germination, recovery germination, and total germination of H. persicum were much lower when seeds were submerged in 700 mm NaCl, especially for the recovery germination and total germination of nongerminated seeds when the seeds were desiccated and then transferred to distilled water. However, when the seeds were submerged in 700 mm NaCl with aeration, the seed germination, recovery germination, and total germination of nongerminated seeds transferred to distilled water increased dramatically for H. persicum. No adverse effect of desiccation was found on those values of nongerminated seeds pretreated in NaCl with or without aeration for the two halophytes. In conclusion, seeds of the two halophytes were more tolerant to waterlogging and dry–moist cycles than seeds of the xerophyte during emergence under saline conditions; these traits may be important for halophytes to survive extreme saline environments during the seed germination stage.  相似文献   

19.
After 120 yr of burial in moist, well-aerated sand, 23 seeds of Verbascum blattaria and two seeds of a Verbascum sp. germinated and produced normal plants (50% germination for Verbascum). After a 6-wk cold treatment, a single seed of Malva rotundifolia germinated also, producing a normal plant (2% germination). Plants were grown to maturity in a greenhouse, and flowering was induced by exposure to a 6-wk cold treatment. Flowers were artificially pollinated to produce seed of both Verbascum blattaria and Malva rotundifolia. The Verbascum sp. failed to set seed. Collected seeds were subsequently germinated, producing normal plants. F(1) seeds of V. blattaria had a germination of 64%. Seeds (6%) of M. rotundifolia germinated after a cold treatment.  相似文献   

20.
The seeds of Fraxinus excelsior L. are dormant after harvest, since they need a period of chilling for germination. Moist treatment at 20°C for 2–3 months followed by stratification at 4°C for 7 months breaks dormancy. We observed that germination occurred during stratification and was spread over a period of 3 months. Germination at low temperature was temporarily inhibited by a moderate reduction of the seed water content initiated after the third month of stratification. This allowed the afterripening process to continue.
The following procedure was developed to suppress dormancy and to induce uniform germination:
  • 1. 

    Imbibition of the seeds and moist treatment at 20°C for 2–3 months;

  • 2. 

    stratification for 3 months;

  • 3. 

    treatment at low temperature and low water potential for at least 4 months, this treatment should not exceed 6 months;

  • 4. 

    complete rehydration of the seeds at 16°C.

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