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1.
东北刺人参(Oplopanax elatus Nakai)种子透水性良好,休眠后萌发不受其影响。种皮和胚乳的水提取物中存在萌发抑制物质,胚乳中提取物对白菜种子萌发的抑制效果比种皮更明显。种子自然脱落时胚尚未分化完全,处于心形胚阶段。种子需要先温暖层积以完成胚的分化与生长,然后转入低温层积完成生理后熟。同批种子胚的发育不完全同步,变温层积处理7个月有极少数种子萌发,连续变温层积处理17个月大部分种子萌发。不同年份受气候条件影响,种子产量和发芽率差异较大。种子耐贮性较强,贮藏2年的种子生活力变化不大,仍具有较高的萌发潜力。  相似文献   

2.
刺五加种子结构,后熟作用及其细胞化学研究   总被引:18,自引:0,他引:18  
刺五加种子为扁肾形,种皮由一层细胞构成。种子脱落时,胚处于心形胚期,胚周围的胚乳细胞解体形成囊腔包囊胚,胚细胞原生质浓厚,胚乳细胞中贮存大量蛋白质和脂类,但两者均未见贮存多糖,有萌发潜能的种子只占全部种子的12.80%,种子经变温层积处理6个月即可完成后熟过程,其细胞化学特点是:处理1.5个月时胚细胞中开始积累多糖颗粒,至4个月时达最大量并一直保持至种子萌发。试验地种植条件下饱满种子经18-20个  相似文献   

3.
山茱萸种子的休眠原因与萌发条件   总被引:8,自引:1,他引:7  
山茱萸种子的萌发受到种皮抑制物、胚生理后熟程度以及当年低温的阻抑。种子秋播后需经3个月高温(15~22℃)、2个月低温(5~16℃)的湿沙层积,才能完成生理后熟,于次年春天萌发。并研究了种子层积过程中氧的作用、种皮的单宁和ABA含量、胚乳转化、G6PDH(6—磷酸葡萄糖脱氢酶)和 6PGDH(6—磷酸葡萄糖酸脱氢酶)与萌发的关系。  相似文献   

4.
珍稀濒危植物金丝李(Garcinia paucinervis)种子的萌发十分缓慢,探讨其休眠机理,可为该物种的种质资源保育与可持续利用提供理论依据。本文对金丝李种子种皮结构及其透水性,剔除部分种皮和胚乳后种子的萌发情况,胚乳和胚等粗提物的活性,储藏、层积和不同温度下种子萌发情况,萌发过程中内源激素含量等进行了研究。结果表明:金丝李种皮无栅栏细胞层,下表面的角质层较薄;种皮对种子的吸胀阻碍小;随着种孔端剔除种皮和胚乳程度的加深,金丝李种子的萌发进程逐渐延长,甚至降低其萌发率,种脐端削除处理对种子萌发影响不大;内果皮、种皮、胚乳和胚中可能存在抑制金丝李种子萌发和生长的内源抑制物;新鲜种子胚率达86.12%,低温层积后胚率无显著变化;低温层积处理延缓其萌发进程,对萌发率无显著影响,4℃低温层积是储藏金丝李种子的较好方法;种子萌发对温度敏感,在32℃培养下可打破种子休眠,萌发速度显著加快。种子萌发过程中ABA含量降低,GA与ABA、IAA与ABA的比值随种子萌发显著升高,萌发促进与抑制物比例逐渐趋于提高。因此,金丝李种子存在内源抑制物,同时缺乏萌发促进物质,导致生理休眠。该种子休眠特性使其幼苗生长能应对生境的季节变化,种群在风险环境中得以延续,避免大量幼苗竞争。植被破坏导致种子萌发阶段受阻是造成金丝李濒危的原因之一。  相似文献   

5.
短柄五加种子结构、后熟作用及其细胞化学研究   总被引:7,自引:0,他引:7  
短柄五加Eleutherococcus brachypus Harms种子为扁肾形,种皮由一层细胞构成。种子脱落时,胚 为心形胚期,胚周围的胚乳细胞解体形成液样囊腔,并包裹胚,胚细胞中存在较多蛋白质,胚乳细胞贮 存大量蛋白质颗粒和脂类,但两者均未见多糖颗粒。有萌发潜能的种子只占全部种子的9.27%。在试 验地种植条件下饱满种子经18~19个月后萌发,出苗率为1.67%,该过程细胞化学特点是胚细胞中蛋 白质含量逐渐减少,并逐渐积累少量多糖颗粒。种子经变温层积处理6个月即可完成后熟过程,其细胞 化学特点是胚细胞中蛋白质含量逐渐减少,但在心形胚后期即已积累大量多糖颗粒,并一直保持至胚 完全发育成熟。经比较短柄五加与刺五加的种子结构、后熟作用及其细胞化学特点,认为短柄五加种子质量差、自然状态下后熟时间长和出苗率低是短柄五加致濒的重要生殖因素,并提出了相应保护方法。  相似文献   

6.
本文观察了短梗南蛇藤种子的形态和萌发过程,研究了温度、层积方法和时间、假种皮浆液、光照等对短梗南蛇藤种子萌发的影响。结果表明,短梗南蛇藤种子对温度较敏感,较适合萌发的温度为15~20℃。低温层积和变温层积均能显著提高种子发芽率、发芽势和发芽指数,层积20d效果最好。假种皮浆液联合层积处理对种子萌发有显著促进作用,其中联合低温层积20d或联合变温层积10d效果最好。光照在一定程度上抑制种子萌发。  相似文献   

7.
红松种子抑制物质的初步研究   总被引:5,自引:0,他引:5  
本文研究了红松种子抑制物质的提取方法,并测定了抑制物质的总活性,以及分布在种子各部位(外种皮、内种皮、胚乳、胚)抑制物质的相对活性。从红松种子各部位提取的抑制物质,不仅对油菜种子萌发和油菜幼根生长有抑制作用,而且也对其层积后解除休眠变黄的红松离休胚有明显的抑制作用。 通过红松种子各部位抑制物质变化动态的初步测定,表明了红松种子的休眠可能与发芽的抑制物质存在有关系。干藏红松种子各部位提取物在层析谱上 R_f值为 0.6的区段都有明显的抑制作用。除此而外,外种皮提取物在R_f值0.7区段,胚提取物在R_f值0.4、0.9区段也有明显的抑制作用。但干藏种子经过层积之后(即层积种子),各部位提取物与上述区段R_f值相比,其抑制作用有明显的下降。尤其是层积红松种子外种皮抑制物质基本消失或显著减少。 抑制物质常温下易溶于 95%乙醇、丙酮、水,其次是甲醇和乙醚,难溶于氯仿,不溶于苯。对高温(100℃)较稳定。  相似文献   

8.
青檀种子休眠机理及发芽条件的探讨   总被引:18,自引:0,他引:18  
对青檀 (PteroceltistatarinowiiMaxim .)种子的休眠机理和发芽条件进行了探讨。共设定 5个处理 :剪破种皮、热水处理 (4 0、5 0、6 0和 70℃ )、剪破种皮并变温层积 (0~ 4℃ 16h与 10~ 15℃ 8h)、低温层积 (0~ 4℃ )和变温层积(0~ 4℃ 16h与 10~ 15℃ 8h)。结果表明 ,剪破种皮、剪破种皮并变温层积和热水处理与对照的发芽率均无显著差异 ,说明青檀种子的休眠不是种皮限制所引起的。低温层积和变温层积处理均能打破种子的休眠 ,因而认为青檀种子休眠属于生理休眠。低温层积以 70d为最好 ,发芽率和发芽势分别达 6 7%和 5 5 % ;变温层积以 40d处理效果最好 ,发芽率和发芽势分别达 77%和 5 7%。同时还讨论了 2种层积处理的优缺点  相似文献   

9.
用不同质量浓度GA3浸泡天女木兰种子并结合变温层积处理,应用高效液相色谱法对不同时期种子中4种激素GA3、IAA、ABA、ZR含量进行测定,并测量种胚长和萌发率,以探讨天女木兰种胚发育,内源激素含量变化与种子休眠萌发之间的调控关系,为进一步研究种子休眠机理提供理论基础。结果表明:(1)天女木兰成熟种子胚发育不完全,胚乳内高浓度ABA和低浓度GA3是其休眠的主要原因。(2)GA3处理能促使天女木兰种子提前30d完成形态后熟,并以1 500mg·L-1 GA3处理效果最佳。(3)在变温层积过程,天女木兰种胚发育可分三个阶段:阶段Ⅰ(0~70d)完成种胚进一步分化;阶段Ⅱ(70~120d)种胚快速生长时期;阶段Ⅲ(120~150d)休眠完全解除,种子具备发芽能力。种子能否打破休眠主要取决于阶段Ⅰ和Ⅱ的状况。(4)GA3/ABA、IAA/ABA和ZR/ABA在种子后熟期间的变化同胚生长发育存在一致性,认为内源激素的相对水平对种子休眠具有重要的调控作用。  相似文献   

10.
珙桐种子休眠原因研究初报   总被引:17,自引:0,他引:17  
珙桐内果皮和种子的水浸提液及乙醚提取液中均含有抑制物质;种子中的抑制物活性主要分布在被发达的胚乳包裹着的子叶内。层积一年后,内果皮及种子中的抑制物活性并未完全消失,但已明显减弱。珙桐种胚的形态后熟以胚芽在层积过程中完成形态分化为主要特征。  相似文献   

11.
Developing seeds of alfalfa (Medicago sativa L.) acquire the ability to germinate during the latter stages of development, the maturation drying phase. Isolated embryos placed on Murashige and Skoog medium germinate well during early and late development, but poorly during mid-development; however, when placed on water they germinate well only during the latter stage of development. Germination of isolated embryos is very slow and poor when they are incubated in the presence of surrounding seed structures (the endosperm or seed coat) taken from the mid-development stages. This inhibitory effect is also achieved by incubating embryos in 10?5 M abscisic acid (ABA). Endogenous ABA attains a high level during mid-development, especially in the endosperm. Seeds developing in pods treated with fluridone (1-methyl-3-phenyl-5[3-(trifluoromethyl)-phenyl]-4(1H)-pyridinone) contain low levels of ABA during mid-development, and the endosperm and seed coat only weakly inhibit the germination of isolated embryos. However, intact seeds from fluridone-treated pods do not germinate viviparously, which is indicative that ABA alone is not responsible for maintaining seeds in a developing state. Application of osmoticum (e.g. 0.35 M sucrose) to isolated developing embryos prevents their germination. Also, in the developing seed in situ the osmotic potential is high. Thus internal levels of osmoticum may play a role in preventing germination of the embryo and maintaining development. Abscisic acid and osmoticum impart distinctly different metabolic responses on developing embryos, as demonstrated by their protein-synthetic capacity. Only in the presence of osmoticum do embryos synthesize proteins which are distinctly recognizable as those synthesized by developing embryos in situ, i.e. when inside the pod. Abscisic acid induces the synthesis of a few unique proteins, but these arise even in mature embryos treated with ABA. Thus while both osmoticum and ABA prevent precocious germination, their effects on the synthetic capacity of the developing embryo are quite distinct. Since seeds with low endogenous ABA do not germinate, osmotic regulation may be the more important of these two factors in controlling seed development.  相似文献   

12.
The Arabidopsis endosperm consists of a single cell layer surrounding the mature embryo and playing an essential role to prevent the germination of dormant seeds or that of nondormant seeds irradiated by a far red (FR) light pulse. In order to further gain insight into the molecular genetic mechanisms underlying the germination repressive activity exerted by the endosperm, a "seed coat bedding" assay (SCBA) was devised. The SCBA is a dissection procedure physically separating seed coats and embryos from seeds, which allows monitoring the growth of embryos on an underlying layer of seed coats. Remarkably, the SCBA reconstitutes the germination repressive activities of the seed coat in the context of seed dormancy and FR-dependent control of seed germination. Since the SCBA allows the combinatorial use of dormant, nondormant and genetically modified seed coat and embryonic materials, the genetic pathways controlling germination and specifically operating in the endosperm and embryo can be dissected. Here we detail the procedure to assemble a SCBA.  相似文献   

13.
Abstract

Alpine plants have evolved to fit their life cycle into the short vegetative season of mountain habitats. Fritillaria tubiformis Gren. & Godr. subsp. moggridgei (Boiss. & Reuter ex Planch.) Rix (Liliaceae) is an endemic alpine geophyte, bearing seeds with underdeveloped embryos. Seeds are dispersed in August and embryos complete their development by spring when seeds germinate. In order to optimize seed banking procedures and to develop a proper germination protocol for plant regeneration, we studied embryo morphogenesis and analyzed how this process is influenced by temperature. Radicle protrusion occurred after an incubation of 5 months at 4°C. Under these conditions, underdeveloped embryos reached maturity and acquired a well-defined shoot apex. At the time of dispersal, abundant storage compounds were present in seeds. Lipids and lipid/proteins were uniformly distributed within the embryo and the endosperm, respectively. At late stages of embryo development, starch granules were localized at the cotyledonary tip and were also detected around the shoot meristem. Results suggested that F. tubiformis embryos resumed growth over a large range of temperatures, but were only able to complete development at low temperatures after which they were able to germinate by spring.  相似文献   

14.
Rosana M. Kolb  Carlos A. Joly 《Flora》2010,205(2):112-117
Tabebuia cassinoides (Lam.) DC (Bignoniaceae) is an arboreal species common in seasonally or permanently waterlogged areas of the “restinga” forest (a type of forest that occurs on the sandbanks of the coastal plains of southeastern Brazil). The objectives of the present study were to establish seed germination responses of this species to flooding and anoxia and investigate the end products of the anaerobic metabolism of seeds subjected to these conditions, with the goal of understanding the adaptive strategies that enable this species to dominate flood prone areas of “restinga”, as well as determine reserves stored in their seeds. Seeds of T. cassinoides did not germinate under anoxia or complete submergence, but remained viable under these conditions for 15 and 20 days, respectively. Due to their membranaceous wings, the seeds float very well and reached 100% germination in this condition, an important adaptation to overcome the initial stages of development in flooded habitats. In relation to anaerobic metabolism, ethanol is the most important end product, while lactate is produced in lower concentrations. Seeds of T. cassinoides have very little endosperm and the reserves, mainly glycoproteins, lipids and free sugars, accumulate in the cotyledons. Free sugars may provide the substrate for the initial metabolism of seed germination, but the level of these reserves was not enough to allow germination under oxygen deprivation. Possibly, carbohydrate reserves were enough only to maintain seed viability for a relative short period under this condition.  相似文献   

15.
该文研究了野外条件下不同深度的沙埋对沙鞭(Psammochloa villosa)种子萌发和幼苗出土的影响,以及温室条件下种子大小对不同深度沙埋后的种子萌发和幼苗出土的影响。结果表明,沙埋深度显著影响沙鞭的种子萌发率、幼苗出土率和种子休眠率。沙子表面的种子不能萌发。2 cm的浅层沙埋时的种子萌发率和幼苗出土率最高,1 cm 沙埋的种子萌发率和幼苗出土率次之。沙埋深度超过2 cm之后,沙鞭的种子萌发率和幼苗出土率与沙埋深度呈负相关。2 cm的种子休眠率最低。从2 ~12 cm,种子休眠率随着沙埋深度的增加而增加。在幼苗能够出土的深度(1~6 cm),幼苗首次出土所需的时间随着沙埋深度的增加而延长。种子大小对沙鞭的种子萌发率没有显著影响。但是在深层沙埋(6 cm)时,与小种子相比,大种子产生的幼苗的出土率较高。从2~6 cm,大种子形成的幼苗的茎长度都较长。  相似文献   

16.
The dormancy breaking and storage behavior of Garcinia cowa Roxb. seeds were investigated.The seeds of G. cowa had 8-11 months dormancy in their natural habitat. Seeds were matured and dispersed at the end of the rainy season (mid-late August to late September) and were scatter-hoarded by rodents as food for winter after the seeds had fallen to the ground. Seedlings often emerged in the forest during the rainy season (May to August) the following year. Intact seeds of G. cowa failed to germinate after being sown at 30 ℃ for 120 d and the mean germination time (MGT) of seeds cultured in a shade (50% sunlight)nursery was 252 d. The most effective method of breaking dormancy was to remove the seed coat totally,which reduced the MGT to 13 d at 30 ℃. Germination was also promoted by partial removal of the seed coat (excising the hilum and exposing the radicle) and chemical scarification (immersion in 1% H2O2 for 1 d).Unscarified seeds take up water rapidly in the first 96 h, but water was absorbed by the outside seed coat,without penetrating through it. The moisture content (MC) of G. cowa seeds was high (50% in fresh weight)at shedding. The seeds could tolerate desiccation to some extent, until the MC reached approximately 40%;below that, the viability decreases rapidly and all seeds died at approximately 17% of MC. Seed viability decreased rapidly when seeds were chilled at 4 ℃; germination was 2% after storage for 1 week. Even stored at 10 ℃, seeds began to be damaged after 4 weeks. Seed storage for 1 yr revealed that in both dry (relative humidity (35 ± 5)%) and moist (wet sand) storage conditions, seed viability declined, but germination percentages for seeds stored under moist conditions are better than for seed stored under dry conditions.Because of their low tolerance to desiccation, marked chilling sensitivity and relatively short lifespan, G.cowa seeds should be classified into the tropical recalcitrant category. The ecological implications of dormant recalcitrant seeds and cues on storing recalcitrant seeds were discussed.  相似文献   

17.
Seeds of both Salsola imbricata and Haloxylon salicornicum have high germination level and germination speed, and form a transient seed bank in nature. The impacts of storage period and condition on germination level and speed were assessed in the two species. Storage for three months significantly increased both germination level and speed of seeds stored under the different conditions, compared to that of fresh seeds. In both species, nine months storage did not affect germination percentage in cold storage seeds, but completely inhibited it in field seeds. Storage for longer time in room and warm temperatures resulted in significant reduction or complete inhibition in the germination of the two species, so this was more pronounced in H. salicornicum. Storage significantly increased germinate rate index of seeds stored in all conditions till 17 months in S. imbricata and till 12 months in H. salicornicum. In both species, fridge storage had little effects on final germination and germination speed of seeds incubated at the different temperatures, compared to fresh seeds. However, room temperature and warm storages significantly reduced final germination and germination speed at the different temperatures, so the reduction was more pronounced at 35 °C, especially in H. salicornicum.  相似文献   

18.
The integrity of ribosomal RNA (the percentage of complete, un-nicked molecules) in seeds was studied by electrophoresis under denaturing conditions. Two batches of carrot seed, harvested at different stages of maturity, and four batches ofNicotiana seed stored for various times were used. Within each species, there was a correlation between the integrity of the rRNA of the dry seed and the rate of germination of that seed. In carrot seed, there was extensive degradation of existing rRNA in both the embryo and endosperm during the first two days of imbibition.  相似文献   

19.
Seed germination time course and seedling development mechanisms of Clintonia udensis Trautv. et Mey. (Uvulariaceae) were investigated under experimental condition. Seed germination tests were carried out under four thermal regimes, i. e. 10, 15, 20, and 25°C, after seeds were harvested, and stored at 5°C in wet conditions for 6 months under light‐exposed or shaded conditions. Approximately 63% of all seeds produced had the potential to germinate beyond 4 years and 6 months. The developmental process after germination continued for over 2 years. Phase I: the radicle first breaks through the seed coat 2 years after fructification. Phase II: the radicle becomes much larger with a hypocotyle. Phase III: part of the cotyledon elongates over 20 mm. Phase IV: the plumule further develops in two steps, i. e. the plumule is first formed, while cotyledon is disappearing, and then the plumule appears with second and third radicles, growing with cotyledon.  相似文献   

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