不同发育时期水曲柳种子的形态生理变化及其层积处理后的萌发效应

探讨不同发育时期水曲柳种子的外部形态和生理变化及其层积处理后的萌发效应结果表明：水曲柳开花120d后为成熟脱水阶段,开花110d后种子的胚长和胚乳干重趋于稳定,花后110～120d期间种子胚干重趋于稳定;花后70～100d采集的种子不耐层积,层积处理后逐渐死亡,花后110d采集的种子经层积处理后可以萌发;110d后采集的水曲柳种子经暖温（20℃）16周＋低温（5℃）12周的层积处理后,其休眠破除的效果较好,适当延长暖温层积时间有利于提高种子萌发率。     

莎草科4种植物种子休眠与萌发特性的研究

以嵩草、黑穗苔草、藨草和苔草4种莎草科植物种子为材料,研究了硫酸、植物生长调节剂及低温层积处理对其休眠与萌发特性的影响,以揭示其休眠机制及其破除方法,为指导生产提供理论依据。结果表明:(1)4种参试植物种子均存在不同程度的生理休眠,其中嵩草为浅度生理休眠,黑穗苔草为中度生理休眠,藨草和苔草为深度生理休眠。(2)浓硫酸浸种可显著提高嵩草、黑穗苔草种子的萌发,随浸种时间增加,种子萌发率先增加后降低,最大值分别达86%、77%,但浓硫酸处理对藨草和苔草的种子萌发无显著促进作用。(3)赤霉素(GA3)、氟啶酮(FL,脱落酸抑制剂)和KNO3单独处理可显著提高嵩草种子萌发,但对其他3种植物种子无显著作用;而硫酸处理后再用赤霉素或氟啶酮处理,则显著促进黑穗苔草种子的萌发率。(4)低温层积对种子萌发的影响因种与层积时间而异,层积2个月可显著提高嵩草种子萌发,层积4个月可显著提高嵩草和藨草种子萌发;层积6个月可显著提高嵩草、黑穗苔草、藨草和苔草4种植物种子萌发,其最终萌发率分别为90%、73%、17%、7%。     

濒危植物西康玉兰种子休眠、萌发及贮藏特性

研究了西康玉兰(Magnolia wilsonii)种胚的形态大小,温度、层积、硝酸钾、浸种处理和GA_3对种子休眠及萌发的影响.通过将种子脱水至不同含水量和在两种温度(4℃和一20℃)下贮藏100 d后测其生活力,分析各处理对西康玉兰种子活力的影响.结果表明:西康玉兰种子胚尚未分化完全,需经过低温层积完成生理后熟;低温层积和GA3可打破种子休眠.种子最适萌发温度为25/20℃.由此推测,西康玉兰种子具有形态生理休眠特性.西康玉兰种子当含水量降至5.39%,存活率为53.50%.不同含水量的种子贮藏在-20℃条件下,100 d后种子全部死亡;但在4℃下含水量为10.31%的种子存活力高达76%.因此,西康玉兰种子极可能属于中间性种子,其适宜贮藏环境为4℃下的干藏或湿藏.     

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。     

东北刺人参种子萌发影响因子的研究

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。     

短梗南蛇藤种子的萌发特性

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。     

珍稀濒危植物金丝李种子的休眠机理

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。     

东北刺人参种子萌发影响因子的研究

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.     

短命植物独行菜种子萌发过程对低温的耐受特性

以独行菜（Lepidium apetalum）为材料,研究了其种子在萌发过程中耐受低温的特性,并对耐受低温的机制作了初步的探讨。结果表明：1.萌发至I、II、III期的独行菜种子经过冷诱导处理后,对零下低温-5℃、-10℃胁迫具有较强的耐受性,这种耐受性随萌发发展相对有所降低。2.独行菜种子萌发过程中胚根生长速度明显受到低温抑制,但也仍然能够生长。3.适当时间的低温层积能使独行菜萌发势显著提高,对终萌发率影响不大;过长时间的低温层积会使独行菜种子萌发势和最终萌发率降低。4.独行菜种子在4℃条件下不能萌发,但4℃层积2d的种子经25℃处理6h以上后,可耐受4℃低温而萌发,且萌发率随25℃处理时间增加而升高。如果25℃处理时间少于5h则不能在4℃低温下萌发。经4℃层积10d、再经25℃萌发处理1h的独行菜种子就能在4℃低温下萌发。综合分析认为独行菜种子不能耐受4℃低温萌发,原因可能是在露白前存在一个关键的生理阶段,在4℃胁迫逆境中不能越过这个阶段,该阶段之前与之后的萌发过程都能耐受4℃低温,因此对低温胁迫有良好的耐受性。这为探索早春短命植物耐受低温萌发的机制提供了新的思路。     

刺木蓼和长枝木蓼种子休眠的解除及萌发条件

刺木蓼（Atraphaxis spinosa）和长枝木蓼（A.virgata）为蓼科木蓼属灌木,是乌鲁木齐周边植被组成的重要种。这两种木蓼种子成熟后不萌发,处于休眠状态,对其种子进行5℃（黑暗）和野外低温层积处理,结果表明：5℃层积处理能明显提高两种木蓼种子在15/6、20/10、25/15和30/20℃（昼12 h/夜12 h）的萌发率。野外层积处理显著提高了种子在15/6℃的萌发率。刺木蓼和长枝木蓼的种子均为非深度生理休眠,分别经8、6周的低温层积处理后种子休眠得以解除。刺木蓼种子的休眠程度比长枝木蓼深,休眠解除后,种子萌发所需的最低温度降低。这两种木蓼种子经过冬天的低温层积,可以在春天较低的生境温度下萌发。     

Burial of canopy-stored seeds in the annual psammophyte Agriophyllum squarrosum Moq. (Chenopodiaceae) and its ecological significance

Agriophyllum squarrosum Moq. is a dominant annual on sand dunes in the arid regions of central Asia. A high percentage of seeds is retained on dead plants which become covered by moving sand, but little is known about the ecological significance of burial of canopy-stored seeds. We investigated the size and dynamics of the buried canopy-stored seed bank and effects of burial on seed germination. In March (during the windy season), May (beginning of the germination season), and July (middle of the growing season), the number of seeds per square meter in sample plots in the dunes was 623, 223 and 22, respectively, with 54.6, 30.6 and 12.9% of the total seeds retained on buried plant canopies. In a controlled experiment, more seedlings emerged from released (dispersed) than from canopy-stored seeds when burial depth was the same. No viable ungerminated released seeds were found, but 45–80% of the ungerminated canopy-stored seeds were viable. In general, with an increase in applied water germination of released seeds buried at a depth of 1 or 2 cm and of canopy-stored seeds buried at 1 cm increased, but regardless of watering regime few or no released seeds at 4 cm or canopy-stored seeds at 2 or 4 cm germinated. Significantly more seedlings emerged from plants buried in a horizontal than in a vertical position. Seedlings originating from buried canopy-stored seeds on an active dune accounted for only 5.4% of the total seedlings emerging, and most of them emerged later than those from released seeds. Thus, seed release is more effectively postponed in buried than in exposed canopies, and burial of canopy-stored seeds is a mechanism that helps regulate seed germination and seedling emergence of A. squarrosum on active dunes.     

Effects of sand burial on purple sandgrass (Triplasis purpurea): the significance of seed heteromorphism

The effects of sand burial on seedling emergence, growth, and reproduction of the annual dune grass Triplasis purpurea (Walt.) Chapm. were examined. This species matures heteromorphic seeds on panicles enclosed by leaf sheaths along tiller nodes in a characteristic pattern: seeds at the lower nodes are heaviest, whilst those at the upper nodes are lightest. Field excavation of seedlings revealed that seedlings can emerge from seeds buried to 4 cm.In one experiment in an incubator, seeds collected from the upper and lower tiller nodes of glasshouse-grown parental plants were buried in sand at depths of 0, 3, and 6 cm. As expected, the effects of seed depth on seedling growth were due to delayed emergence for seedlings from buried seeds. However, seedlings from the larger seeds from the lower nodes of parental plants had significantly greater dry mass than those from the lighter seeds from upper nodes. Because lower node seeds are the most likely to become buried by sand in nature, the seed heteromorphism may be adaptive in the coastal environment.A second experiment involved the burial of seedlings to 0, 50, or 100% of their height. Although most seedlings did not survive complete burial (100% height), for partially buried seedlings (50% height) there was high survival and a marked stimulation of growth and eventual reproduction compared to unburied seedlings. This stimulation could be linked to increased root growth for seedlings that had been buried. The ability to respond positively to sand accumulation may represent an adaptation to the dynamic dune environment.     

Ignorant seed predators and factors affecting the seed survival of a tropical palm

In addition to acting as seed predators, some terrestrial mammals bury seeds via scatter hoarding. This study system used two permanent plots in examining the interaction between small rodents and the seeds of the palm Astrocaryum mexicanum. We tested how experimental burial, and fruiting status of the parent, distance to the parent, seed size, and microsite characteristics affect the survival of these seeds. Up to 34% of the buried seeds that were exposed only to ignorant rodent foragers (individuals not responsible for burial) survived. In comparison, less than 1% of seeds buried by scatter hoarding rodents survived in previous studies, a percentage that is comparable to the low survival of unburied seeds in this study (<2%). Although unburied seeds had very low survival, increasing distance and/or seed density positively affected survival of unburied seeds. Distance to parent had no effect on buried seed survival.
Buried seed survival was most strongly and significantly determined by the fruiting status of the trees under which they occurred. Seeds experienced significantly greater predation if buried under “parent” trees that fruited during the experiment. Buried seed survival was also negatively affected by germination, as germination may signal the presence of a seed to foraging rodents. There was some indication of a positive effect of tree density on seed survival between the two plots, whereas differences in rodent abundance appear to have no effect on seed survival. Seed size and microsite characteristics had no significant effect on buried seed survival, likely due to the greater proportional effects of other factors and the longevity of A. mexicanum seeds. The results of this study were used to generate a hypothetical causal network showing how comparatively low recovery of buried seeds by ignorant foragers – combined with processes determining the removal of scatter hoarding foragers from their scattered seed caches – may affect seedling recruitment in A. mexicanum.     

同种竞争压力对小泡巨鼠贮藏油茶种子行为的作用分析

2002年11～12月,在四川省都江堰地区的亚热带常绿阔叶林内利用人工修建的半自然状态围栏进行实验,研究了小泡巨鼠在有同种竞争存在条件下对油茶种子的埋藏行为。结果表明,小泡巨鼠在有竞争存在条件下,显增加了埋藏油茶种子的量。这一结果支持了“竞争的存在刺激鼠类埋藏”的假说。同时,研究结果表明,小泡巨鼠在有竞争存在条件下,显增加了对埋藏种子的搬运距离,每个贮藏点埋藏种子的数量也有所增加,同时埋藏的生境更多地偏向于遮蔽较好的微生境(草丛底层、灌丛下层)中。这些行为策略有可能有利于种子被埋藏植物的种群扩散。在讨论中,我们还通过比较鸟类和兽类在感觉器官上的差别,分析它们在有竞争存在条件下所采取的不同贮食策略。     

Seed Dispersal by Monkeys and the Fate of Dispersed Seeds in a Peruvian Rain Forest1

Primary seed dispersal by two species of monkeys and the effects of rodents and dung beetles on the fate of dispersed seeds are described for a rain forest in southeastern Perú. During the six-month study period (June–November 1992) spider monkeys (Ateles paniscus) dispersed the seeds of 71 plant species, whereas howler monkeys (Alouatta seniculus) dispersed seeds of 14 species. Spider and howler monkeys also differed greatly in their ranging behavior and defecation patterns, and as a consequence, produced different seed rain patterns. Monkey defecations were visited by 27 species of dung beetles (Scarabaeidae). Dung beetles buried 41 percent of the seeds in the dung, but the number of seeds buried varied greatly, according to seed size. Removal rates of unburied seeds by rodents varied between 63–97 percent after 30 d for 8 plant species. The presence of fecal material increased the percentage of seeds removed by seed predators, but this effect became insignificant with time. Although seed predators found some seeds buried in dung balls (mimicking burial by dung beetles), depth of burial significantly affected the fate of these seeds. Less than 35 percent of Brosimum lactescens seeds buried inside dung balls at a depth of 1 cm remained undiscovered by rodents, whereas at least 75 percent of the seeds escaped rodent detection at a depth of 3 cm and 96 percent escaped at 5 cm. Both dung beetles and rodents greatly affected the fate of seeds dispersed by monkeys. It is thus important to consider postdispersal factors affecting the fate of seeds when assessing the effectiveness of frugivores as seed dispersers.     

Litter and seed burying alter food availability and foraging efficiency of granivorous birds in the Monte desert

We assessed experimentally if the main granivorous bird species that feed on the ground in the central Monte desert are able to detect and consume seeds buried in the soil or trapped within litter. Understanding seed vulnerability to birds allows 1) a better understanding of how seed abundance translates into seed availability, a necessary step to assess seed limitation scenarios, and 2) whether birds alter the distribution of soil seeds through their consumption. Rufous‐collared sparrows found and consumed high proportions of buried seeds, though less seeds were eaten at increasing depths. In contrast, many‐colored chaco‐finches, common diuca‐finches and cinnamon warbling‐finches did not find buried seeds. All bird species fed on every substrate offered but, as a whole, birds reduced by 50% their seed consumption in Prosopis litter, and by 30% in Larrea litter, compared to consumption in bare soil. This effect was less notable for rufous‐collared sparrows, whose ‘double scratch’ foraging method would contribute to its great diet breath and abundance in the Monte desert. As birds do not reach a fraction of seeds buried and trapped by litter, seeds readily available for them may be scarcer than previously estimated through soil seed bank studies. Furthermore, since the four bird species detect and consume seeds from littered microhabitats, seed consumption by them surely affects the seasonal dynamics of the soil seed bank in all microhabitat types of the Monte desert.     

围栏条件下捕食风险对岩松鼠贮藏核桃种子行为的影响

面对捕食风险,贮藏植物种子的啮齿动物如何通过调整其贮藏行为,权衡捕食风险和贮食效益,需要深入研究。2006 年9 月,在北京东灵山地区,以黄鼬作为捕食风险源,在半自然围栏内比较了有无捕食风险源时,岩松鼠贮藏的核桃种子的状态,以及埋藏种子在实验围栏内的分布、微生境和搬运距离,以探讨捕食风险对岩松鼠贮藏种子行为的影响。结果表明,捕食风险源存在时,搬运和埋藏种子的比例都显著减少,弃置地表种子的比例无显著差异;埋藏于高风险区的种子比例减少,中风险区和低风险区的埋藏种子比例增加,但差异都不显著;位于裸地和草下的埋藏种子比例减少,位于墙基的埋藏种子比例增加,但差异都不显著;此外,埋藏种子的搬运距离也没有显著差异。可见,捕食风险源存在时,岩松鼠显著减少了搬运和埋藏种子的比例,但对埋藏种子时的埋藏区域和微生境选择,以及搬运距离无显著影响。差异不显著可能与围栏效应有关。     

红松阔叶林中红松种子的分布及更新

天然阔叶红松林的红松种子经过动物活动的处理,在林内呈四个层次的垂直分布．其中在地被物下是以簇状埋藏着,数量相当多,尤其在红松密林中高大树木的周围,这些簇状分布的种子成为红松天然更新的基础。在次生阔叶林中红松种子埋藏量则很小。而埋藏位置与红松幼苗适生生境的不吻合是红松天然更新的主要障碍。     

The ecology of the seed in Trapa natans var. Japonica in a eutrophic lake

The production, density and environment of buried seeds and the temperature response of germinating seeds in Trapa natans var. japonica Nakai were ascertained. The mechanism of high reproductivity, tolerance of the plant for eutrophication and the stability of the stand in an eutrophic lake are discussed. The mean fresh weight of seeds was about 7.2 g, and the density of liver and dead seeds in April ranged 66.7 to 80.0 m^-2 and 26.7 to 97.8 m^-2, respectively. The threshold temperature that breaks dormancy and promotes germination in the lake was the low temperature, 8°C. The dormancy of buried seeds was almost broken under the field condition in January. The rate of germination obtained by the field experiment, and the estimation from the density of buried seed and the number of seeds germinated at the stand, were 87% and 60%, respectively. It was estimated that about 30% of the seedlings died before the floating leaf reached water surface. A rosette produced less than three seeds a year, which were fewer than for another Trapa, but the size of the former was larger. The number of seeds changed year by year, but the size-distribution pattern of seeds did not change with years, nor was it affected by the density of rosettes. The reason why T. natans var. japonica could succeed in eutrophic waters was attributed to reproductive strategy. The stand could recover by increasing the number of rosettes through the great branching ability of the main stem, even when the density of buried seeds was greatly decreased in the previous year.     

果肉和埋土深度对新疆野杏种子萌发与幼苗生长的影响

为探明新疆野杏（Armeniaca vulgaris）种子萌发与幼苗生长对果肉和埋土深度的响应,以期为新疆野杏的天然更新与实生苗培育提供理论参考。通过2种果皮结构（有果肉和无果肉）的种子在不同埋土深度（地表至18.0 cm的14个梯度）对新疆野杏种子萌发和幼苗生长进行研究,旨在揭示果皮结构和埋土深度对新疆野杏种子萌发与成苗能力的影响。结果表明：果肉和埋土深度显著影响野杏种子的萌发、幼苗生长与质量（P<0.05）。埋土深度<3.0 cm不利于成苗,埋土深度>6.0 cm时,萌发能力与幼苗生长量随埋土深度的增加而降低,3.0～6.0cm为适宜埋土深度。无果肉种子萌发优于有果肉种子,萌发率、萌发指数、成苗率、活力指数分别增长了37.18%、3.88%、37.18%、26.59%,幼苗高、基径、叶片数量、根冠比、幼苗质量指数分别增长了36.99%、7.48%、68.69%、20.61%、14.29%,其萌发能力与幼苗生长量显著高于有果肉种子（P<0.05）。有无果肉种子的萌发和幼苗生长指标与埋土深度呈显著负相关（P<0.05）。研究结果表明,无果肉处理对新疆野杏种...