温度、光照和盐分对外来植物黄顶菊种子萌发的影响

对黄顶菊(Flaveria bidentis)种子的表面形态进行了扫描电镜观察,并从温度、光照、NaCl胁迫及浸种等方面对黄顶菊种子萌发特性进行了探讨.结果表明:黄顶菊种子喜高温,35℃下种子萌发迅速,且发芽率、发芽指数及活力指数最高;光照对种子发芽率影响不大,但随光照时间延长,种子发芽高峰推迟且峰值下降,发芽指数和活力指数逐渐下降;随NaCI浓度升高,种子发芽高峰推迟日.峰值变小,发芽率也呈下降趋势,但低NaCl浓度(0.01 mol/L和0.05 moi/L)胁迫下种子发芽率仍保持在90%以上,且促进了种子发芽指数及活力指数提高及胚根的伸长,结合天津地区黄顶菊生境中土壤的含盐量的分析表明,黄顶菊具有相当强的耐盐性;浸种对种子发芽率和发芽指数影响也很大.因此,黄顶菊成为潜在入侵种与其种子极高的萌发率及耐受高温和盐碱等特性密切相关.     

横断山区干旱河谷川滇蔷薇种子休眠与萌发的地理空间差异

通过测定横断山区干旱河谷18个川滇蔷薇种群新采集种子以及低温层积8周种子的发芽率和发芽速度,分析发芽率和发芽速度与种子特征以及环境因子之间的关系,阐明川滇蔷薇种子休眠与萌发的地理空间差异及其影响因素。结果表明,18个川滇蔷薇种群种子具有不同程度的休眠,新采集种子发芽率变化幅度大,为15.8%±5.0%至82.7%±2.3%,发芽速度指数范围：2.3%±0.2%至5.3%±0.5%。不同种群种子发芽率和发芽速度差异显著。新采集种子的发芽率在流域间存在显著差异,表现为金沙江流域 > 雅砻江流域 > 大渡河流域和岷江流域。新采集种子的发芽率和发芽速度随着采集地点海拔的升高而显著增加,即种子休眠程度随着海拔的升高呈现降低趋势。低温层积8周显著提高了种子发芽率和发芽速度,但减弱了种子发芽率和发芽速度在流域以及海拔间的差异。偏相关分析表明：瘦果皮厚度与新采集种子萌发速度成显著负相关关系;环境因子中年蒸发量与发芽率以及发芽速度之间关系最为密切,成极显著正相关关系;其次为年降水量,与发芽率和发芽速度之间具有显著的负相关关系。综合分析表明,川滇蔷薇种子休眠与萌发在横断山区干旱河谷存在较强地理空间差异。环境因子中年蒸发量和年降水量以及植物自身特征瘦果皮厚度是引起种子休眠与萌发地理空间差异的主要因素。     

扁蓿豆和苜蓿种子萌发期抗旱性和耐盐性比较

为明晰扁蓿豆[Medicago ruthenica(Linn.)Trautv.]和苜蓿(Medicago varia Martin.)种子萌发期的抗旱性和耐盐性强弱,以不同浓度的聚乙二醇(PEG-6000)和Na Cl溶液模拟干旱和盐胁迫,研究了不同程度干旱和盐浓度对采自甘肃景泰的扁蓿豆和苜蓿品种阿尔冈金(M.varia Martin.cv."Algonquin")种子萌发和幼苗生长的影响。结果表明,干旱胁迫和盐胁迫降低了扁蓿豆和苜蓿种子的发芽率、发芽指数、活力指数,抑制了胚芽和胚根的生长。-0.3~-0.9 MPa和-1.5 MPa的PEG处理下苜蓿和扁蓿豆种子的相对发芽率间无显著差异,-1.2 MPa的PEG胁迫下苜蓿种子的相对发芽率显著高于扁蓿豆。-0.3~-1.2MPa的PEG胁迫下苜蓿种子的相对发芽指数均显著高于扁蓿豆,其相对芽长无显著差异。Na Cl渗透势为-0.9~-1.5 MPa时,苜蓿种子的相对发芽率显著高于扁蓿豆;-0.3~-1.2 MPa的Na Cl胁迫下苜蓿种子的相对发芽指数和相对活力指数均显著高于扁蓿豆。通过种子萌发期的相对发芽率、相对发芽指数、相对活力指数、相对胚根长和相对胚芽长5项指标,应用隶属函数法对参试材料种子萌发期抗旱性和耐盐性进行综合评价的结果表明,苜蓿品种阿尔冈金种子萌发期的抗旱性、耐盐性均强于来自景泰的扁蓿豆。此结果和人们以往对扁蓿豆和苜蓿的认识"扁蓿豆的抗旱性和耐盐性优于苜蓿"不一致。     

温度和种子大小对黄花委陵菜种子萌发特征的影响

种子萌发是一个代谢过程,受到种子自身的内在因素和外界环境因素的双重作用。影响种子萌发的主要内在因素是种子大小,主要外在因素是外界环境温度。本研究以黄花委陵菜种子为材料,进行了温度和种子大小对种子发芽影响的研究。结果表明:温度显著影响种子的发芽率、发芽势和发芽指数。20℃是黄花委陵菜种子的发芽率、发芽势和发芽指数最高。种子大小只与其发芽率有显著关系,未能显著改变发芽势和发芽指数。综合各项指标,黄花委陵菜的最适发芽温度是20℃,温度适应范围比较小,在园林育种、管理等应用方面要严格控制其外界温度变化。     

西双版纳桑寄生植物的繁殖

桑寄生植物的种子无休眠期,在果实内可以发芽。月平均温度15—26℃,相对湿度78—88％时,种子在多种死、活物体上均能发芽,总平均发芽率87.3％;极大多数种子在室温18—32℃时、2—8天发芽,发芽率97.3％;冰箱内温度4—5℃时,10—31天发芽,发芽率78％,但发芽种子移室温下不再继续生长。去果肉的种子发芽时间短,发芽率比带果肉的种子高。室内弱光照下的种子发芽率比不见光的高。桑寄生的幼苗只能在其寄主树上生长成株,完成生命周期。人工栽培必须用新鲜果实内的种子,在适宜的温湿度和光照下,播种在其寄主树的小枝上。从播种至开花结果约需1.5—3年。     

光照和不同药剂浸种对龙葵种子发芽率的影响

为探索超富集植物龙葵种子的快速发芽方法,以滤纸为发芽基质,采用恒温培养箱及温室培养的方法,对龙葵种子进行不同浸种处理,探讨光照及不同浸种液对龙葵种子发芽的影响.结果表明: 光照条件是龙葵种子发芽的重要条件之一,光照条件下的发芽率约为无光照条件下发芽率的5倍(P<0.05);不同浸种液均能显著提高龙葵种子的发芽率,其中以双氧水的处理效果最好,发芽时间最短(P<0.05);浸种后不经清洗处理的龙葵种子发芽率约为浸种后再经清洗处理发芽率的2～3倍(P<0.05).     

浓硫酸处理对海滨木槿10个家系种子萌发的影响

以海滨木槿10个家系种子为材料,采用浓硫酸不同时间(0、10、15和20 min)处理,测定种子发芽率、发芽势、发芽指数及萌发过程中相对吸水率、可溶性糖、淀粉和α-淀粉酶含量,研究浓硫酸处理对海滨木槿种子萌发的影响以及不同家系间种子萌发差异.结果表明:浓硫酸处理显著提高了海滨木槿种子的发芽率、发芽指数和发芽势,缩短了发芽时间.浓硫酸处理15 min后,种子发芽率、发芽势和发芽指数分别为95.7％、91.3％和13.28,萌发时间最短,效果最佳.海滨木槿不同家系间种子发芽率、发芽势和发芽指数差异显著,最高发芽指数(15.13)是最低发芽指数(7.15)的2.12倍,最高发芽势(98.0％)是最低发芽势(55.5％)的1.77倍.浓硫酸处理可加快海滨木槿种子萌发代谢生理生化进程.相对吸水率、可溶性糖和α-淀粉酶均呈单峰曲线变化(先升后降),在萌发初期达到最大值;淀粉含量与种子发芽指数呈显著负相关.     

不同贮藏条件和发芽方法对羊草种子萌发的影响

贮藏条件(温度、水分和贮藏介质)和发芽方法(发芽床种类×播种方法)是影响羊草种子萌发的重要因素.研究了4种贮藏条件(4 ℃低温干贮、自然室温干贮和非盐碱土低温湿贮、盐碱土低温湿贮)、3种发芽床(滤纸、非盐碱土与盐碱土)和2种播种方法(表面与内部播种)对羊草种子发芽率的影响.结果表明,与室温干贮相比,低温干贮可以提高羊草种子的发芽速率和整齐度,但对最终发芽率没有显著影响.盐碱土低温湿贮显著降低羊草种子发芽率(28.8%);非盐碱土低温湿贮可显著提高羊草种子的发芽率(73.7%).6种组合发芽方法的发芽率大小和顺序依次为：非盐碱土表发芽法(89.3%)>纸间发芽法(68.0%)>纸上发芽法(64.0%)>非盐碱土内发芽法(61.3%)>盐碱土表发芽法(25.6%)>盐碱土内发芽法(6.0%).     

旱生灌木岷谷木蓝种子的休眠与萌发特征

岷谷木蓝(Indigofera lenticellata)是横断山区干旱河谷广泛分布的豆科灌木.本文对其种子的休眠与萌发特征进行了研究.结果表明:岷谷木蓝种子具有物理休眠,其萌发困难的原因在于种皮的不透水性;种子的硬实比率高(85%),针刺种皮和沙摩处理能有效打破种子休眠,提高发芽率,其中沙摩7 h最为快速有效.岷谷木蓝种子发芽温度范围较广,10℃～30℃均可发芽,最适温度范围为20℃～30℃,低温不利于种子萌发.岷谷木蓝具有一定的抗旱性,在聚乙二醇6000(PEG)溶液模拟水分胁迫条件下,种子在25% PEG胁迫下仍能达到100%的发芽率,但水分胁迫对种子发芽有一定的延缓作用,发芽率和发芽速度降低,发芽周期和发芽准备期增长,发芽高峰期滞后.其中对于发芽能力检测的各项指标对水分胁迫的敏感性顺序为发芽指数>发芽势>发芽率.岷谷木蓝种子的发芽特征是对干旱河谷生存环境长期适应的结果.野外播种的适宜时间为4月初,并在播种前对种子进行7 h的沙摩处理.     

板蓝根种子的吸水特性及发芽条件研究

采用室内测定方法,对板蓝根种子的吸水特性及不同处理下种子的发芽率、发芽势和相对活力指数等进行比较研究。结果表明,板蓝根种子具有快速吸水的生物学特性,分为快速吸水期、缓慢吸水期和缓慢吐水期三个阶段,入水后2 h的吸水量达最大吸水量的73.29%,为快速吸水阶段;温度对板蓝根种子的萌发影响较大,最适发芽温度为30℃。光照、发芽床和种子预处理对板蓝根种子的萌发无明显影响。这说明板蓝根种子的萌发主要取决于水分和温度。     

快速打破结缕草种子休眠方法的比较

用水和30%NaOH对结缕草(Zoysia japonica Steud.)种子进行浸种处理,筛选能快速打破结缕草种子休眠的方法.结果表明:用水浸种6d,8d内发芽率仅为14.70%;用30%NaOH浸种120min,8d内发芽率也仅达28.00%;而用水浸泡2d后再用30%NaOH处理40min,8d内结缕草种子的发芽率达到了82.00%.说明用水和30%NaOH综合处理的方法可以快速有效打破结缕草种子休眠,缩短发芽周期,达到快速出苗的目的.     

A meta-analysis of the effects of frugivory (endozoochory) on seed germination: role of seed size and kind of dormancy

Heretofore, no study has determined how germination of ingested seeds is affected by the kind (class) of dormancy nor by seed dormancy x seed size interaction. Thus, we aimed to determine the effects of seed size, kind of dormancy and their interaction on germination of defecated seeds using a meta-analysis. We collected data for 366 plant species in 97 plant families from 76 publications. In general, gut passage significantly increased germination percentage of defecated seeds by 5% compared with that of control seeds. Germination percentages of non-dormant, physiologically dormant, and morphologically/morphophysiologically dormant seeds (all water-permeable) significantly decreased after gut passage by 40, 18, and 14%, respectively, compared with control seeds (non-gut-passed). Changes in germination percentage of seeds with physical dormancy (water-impermeable) were positive, and gut passage increased germination by 69% compared with control seeds. Germination of small seeds decreased 8% after gut passage, whereas germination of both medium and large seeds increased by 18%. However, changes in germination percentage differed between categories of seed size in each class of dormancy. In physically dormant seeds, germination of all seed sizes improved after gut passage, and the magnitude of increase was higher for large than for medium and small seeds. Thus, gut passage increased germination of medium-size water-permeable seeds (physiologically dormant and morphologically/morphophysiologically dormant) more than it did for large and small seeds. However, gut-passage decreased or did not change the germination percentage of non-dormant seeds. Seed size and kind of dormancy should be included in studies on the effect of gut passage on germination.     

光信号与激素调控种子休眠和萌发研究进展

休眠是种子植物在长期进化过程中产生的适应性性状, 通过抑制种子在不适宜的环境中萌发进而保证植物能够在逆境中生存。此外, 休眠有助于种子的长距离运输和扩散, 因此休眠对种子延续和物种保存具有重要意义。种子由休眠向萌发的发育转变不仅关系到物种的繁衍, 而且对保证农业生产中作物的产量和品质也具有重要作用。种子的休眠和萌发受到内源激素和外源光信号的共同调控。其中, 外源光信号主要通过调控内源ABA和GA的生物合成及信号转导进而调控种子休眠和萌发。该文系统综述了外源光信号和内源激素调控种子休眠和萌发的作用通路以及两类信号通路之间的交互作用, 旨在为农业生产中利用光和激素调控种子休眠与萌发提供参考。     

温带半干旱地区一年生植物种子的萌发特性

在实验室条件下研究了中国温带半干旱地区科尔沁沙地的23种1年生植物的种子萌发特性（新采集种子、冷藏和干藏种子）.大籽蒿、虎尾草、冠芒草、沙蓬和地锦的新种子萌发率达90%左右,11种植物新种子萌发率均低于70%,说明这些植物的新种子具有或多或少的休眠属性.经过150d的冷干藏后,大籽蒿、虎尾草萌发率保持在90%以上,说明这两种植物完全没有休眠机制;冠芒草、沙蓬和地锦的种子萌发率下降较多,可能是储藏的环境条件导致的2次休眠现象;冷藏和干藏处理均能使绿珠藜、毛马唐、细叶益母草、雾冰藜、金狗尾草、苋菜、马齿苋、碱地肤和水稗草的种子在生长季开始时完成生理后熟,萌发率达到80%以上;干藏有利于促进毛马唐、细叶益母草、马齿苋和鹤虱的种子成熟,冷藏有利于促进绿珠藜和金狗尾草的种子成熟;黄蒿、灰绿藜、画眉草和烛台虫实在不同处理下的萌发率都比较低,说明种子内在生理休眠作用较强,具有减少种子一次性萌发数量的风险分摊策略.大多数1年生植物均能在较短时间内达到最终萌发率的90%,表现出迅速萌发的特性;黄蒿、灰绿藜、碱地肤和沙蓬种子则在不同处理中表现出延长萌发时间的策略来适应半干旱地区不确定的环境条件.最后,探讨了几种主要1年生植物的种子萌发对策与其对环境适应机制之间的关系.     

光信号与激素调控种子休眠和萌发研究进展

休眠是种子植物在长期进化过程中产生的适应性性状, 通过抑制种子在不适宜的环境中萌发进而保证植物能够在逆境中生存。此外, 休眠有助于种子的长距离运输和扩散, 因此休眠对种子延续和物种保存具有重要意义。种子由休眠向萌发的发育转变不仅关系到物种的繁衍, 而且对保证农业生产中作物的产量和品质也具有重要作用。种子的休眠和萌发受到内源激素和外源光信号的共同调控。其中, 外源光信号主要通过调控内源ABA和GA的生物合成及信号转导进而调控种子休眠和萌发。该文系统综述了外源光信号和内源激素调控种子休眠和萌发的作用通路以及两类信号通路之间的交互作用, 旨在为农业生产中利用光和激素调控种子休眠与萌发提供参考。     

Are fungi important for breaking seed dormancy in desert species? Experimental evidence in Opuntia streptacantha (Cactaceae)

Seeds of Opuntia spp. have physiological dormancy; they need a period of after-ripening to break dormancy, and the embryos have low growth potential. We evaluated the combined effects of seed age and presence of fungi on the testa on germination of Opuntia streptacantha, an abundant species in the Chihuahuan Desert (Mexico), assuming that older seeds have broken seed dormancy and fungi can reduce mechanical resistance to germination. In a preliminary experiment, we found no germination of 9-year-old (1998) and freshly collected (2007) seeds. However, we obtained 67% and 27% germination from 9-year-old and fresh non-sterilized seeds, respectively, and found fungi growing on the testa of all germinated seeds. Two fungal strains were isolated and identified using ribosomal internal transcribed spacer (ITS) sequence analysis: Penicillium chrysogenum and Phoma sp. In a second experiment, we inoculated seeds with strains of P. chrysogenum and Phoma sp., as well as Trichoderma koningii and binucleate Rhizoctonia (Gto17S2), to evaluate their ability to break seed dormancy. Seeds inoculated with P. chrysogenum, Phoma sp. and T. koningii had higher germination than controls for both seed ages, but germination was higher in older seeds. Scanning electron microscopy showed that these fungi eroded the funiculus, reducing its resistance. Binucleate Rhizoctonia did not lead to germination and controls had almost no germination. Our results strongly indicate that fungi are involved in breaking seed dormancy of O. streptacantha, and that the effect of fungi on seeds is species-specific.     

Deep and intermediate complex morphophysiological dormancy in seeds of Ferula gummosa (Apiaceae)

We tested the hypothesis that seeds of the monocarpic perennial Ferula gummosa from the Mediterranean area and central Asia have deep complex morphophysiological dormancy. We determined the water permeability of seeds, embryo morphology, temperature requirements for embryo growth and seed germination and responses of seeds to warm and cold stratification and to different concentrations of GA₃. The embryo has differentiated organs, but it is small (underdeveloped) and must grow inside the seed, reaching a critical embryo length, seed length ratio of 0.65–0.7, before the seed can germinate. Seeds required 9 weeks of cold stratification at <10°C for embryo growth, dormancy break and germination to occur. Thus, seeds have morphophysiological dormancy (MPD). Furthermore, GA₃ improved the germination percentage and rate at 5°C and promoted 20 and 5% germination of seeds incubated at 15 and 20°C, respectively. Thus, about 20% of the seeds had intermediate complex MPD. For the other seeds in the seed lot, cold stratification (5°C) was the only requirement for dormancy break and germination and GA₃ could not substitute for cold stratification. Thus, about 80% of the seeds had deep complex MPD.     

Delayed germination and dispersal in desert annuals: Escape in space and time

Summary A model is developed to consider the interplay between dispersibility and delayed germination in desert annuals. The model explores the effect of low levels of dispersal, considered realistic for annual plants, on optimal germination fraction. The model also demonstrates the effect of the amount and accuracy of predictive (responsive to the environment) dormancy on the optimal innate germination fraction (not responsive to environmental conditions).Optimal germination fraction is found to be very sensitive to changes in despersibility especially at the limited dispersibilities that are realistic for annual plants. As dispersibility increases, optimal germination fraction increases. If plants make two kinds of seeds with differing despersibility, reproduction is maximized if the low dispersal seeds have delayed germination and the high dispersal seeds have quick germination. If dormancy mechanisms permit seeds to germinate when environmental conditions allow successful maturation, and remain dormant when environmental conditions do not permit successful maturation, what fraction of seeds should remain dormant under predicted good conditions as a hedge against inaccurate prediction of the environment? If environmental cues that break dormancy are uncorrelated with environmental conditions that permit successful maturation, predictive dormancy has little or no effect on the optimal innate germination fraction. When predictive dormancy lowers the probability of germinating when environmental conditions preclude successful maturation, the optimal innate germination fraction increases with increasing germination control by predictive dormancy. With a moderate degree of germination control by predictive dormancy, the optimal innate dormancy is still sensitive to changes in dispersal in the low dispersal ranges characteristic of annual plants.Evidence is presented from plant species that have both dispersal and germination dimorphisms to support the predicted correlation of high germination fractions with high dispersal.     

极度濒危植物大果木莲种子的休眠与萌发

大果木莲种子具吸水性,胚未完全发育。新鲜种子25℃下的萌发率仅2％,在30／20℃和20／10℃的条件下30d内分别有27％和36％种子萌发。在20／10℃下,1000mg·L^-1浓度的GA3可以有效打破种子休眠。冷层积120d的种胚生长不显著,大果木莲种子具有条件休眠特性,属于浅度简单型形态生理休眠。种子经冷层积60d的萌发率最高,而后下降,提示其可能有休眠循环现象。     

贵州毕节喀斯特地区优势植物种子萌发特性初步研究

对采自贵州毕节地区的11种植物的种子萌发特性进行了初步研究,结果表明：①盐肤木、火棘、化香、云贵金丝桃与白栎种子在4周之内能够萌发;除云贵鹅耳枥胚坏死之外（萌发实验前后对种子进行解剖）,其他5种植物的种子都未萌发,处于不同的休眠状态。②盐肤木、化香、云贵金丝桃的种子光照时的萌发率远高于黑暗时的萌发率,具有显著差异,尤其是云贵金丝桃,因此3种植物种子均属于喜光性种子;而火棘与白栎种子有无光照都可以萌发,而且萌发率没显著差异,因此属于光不敏感或光中性种子。③盐肤木、云贵金丝桃的种子在30℃较高温条件下萌发最好;白栎、火棘种子在15℃、20℃低温条件下萌发更好;化香种子萌发温度既不能低于20℃也不能高于25℃。④刺异叶花椒种子吸水率高达85%,胚包埋在胚乳之中非常微小、未分化,因此可以初步判定属于形态休眠或者形态生理休眠;而平枝荀子、西域旌节花、云南旌节花种子吸水率都在20%以上,胚长/种子长都超多1/2,并且胚已发育完全,应属于生理休眠;小果蔷薇种子吸水率约27%,胚长/种子长都达2/3,并且通过对种子的解剖发现胚还未发育,应属于形态生理休眠。