33 resultados para Stratification

em Chinese Academy of Sciences Institutional Repositories Grid Portal


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A new thermoplastic-photoconductor laser holographic recording system has been used for real-time and in situ observation of alpha-LiIO3 crystal growth. The influence of crystallization-driven convection on the concentration stratification in solution has been studied under gravity field. It is found that the stratification is closely related to the seed orientation of alpha-LiIO3 crystal. When the optical axis of crystal seed C is parallel to the gravity vector g, the velocity of the concentration stratification is two times larger than that in the case of C perpendicular-to g. It needs 40 h for the crystalline system of alpha-LiIO3 to reach stable concentration distribution (expressed as tau) at 47.6-degrees-C. The time tau is not sensitive to the seed orientation. Our results provide valuable data for designing the crystal growth experiments ia space.

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Turbulence was generated by an oscillating grid above a bed of sediment of spherical glass beads. As expected, part of the sediment was lifted up by the grid action and a suspension layer of depth D formed above the grid. This depth was found remaining independent of grid action but varying with the sediment layer depth when the grid action was kept constant. Volume concentration measurements show the existence of only weak concentration gradients over the layer depth with a rapid fall off in concentration at the outer edge. The theoretical analysis based on a concentration flux model is in good qualitative agreement with observations.

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In general, competition between buoyancy mechanisms and mixing dynamics largely determines the water column structure in a shelf sea. A three dimensional baroclinic ocean model forced by surface heat fluxes and the 2.5 order Mellor-Yamada turbulence scheme is used to simulate the annual cycle of the temperature in the Bohai Sea. The difference between the sea surface temperature (SST) and sea bottom temperature (SBT) is used to examine the evolution of its vertical stratification. It is found that the water column is well-mixed from October to March and that the seasonal thermocline appears in April, peaks in July and then weakens afterwards, closely following the heat budget. In addition, the Loder parameter based on the topography and tidal current amplitude is also computed in order to examine tidal fronts in the BS, which are evident in summer months when the wind stirring mechanism is weak.

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Existing models of baroclinic tides are based upon the "traditional approximation'', i. e., neglect of the horizontal component of the Earth's rotation, leading to a well- known conclusion that no freely propagating internal waves can exist beyond the critical latitude and the wave rays are symmetric to the vertical. However, recent studies have contended that the situation may change if both the vertical and horizontal components of the Earth's rotation are taken into account. With the full account of the Coriolis force, characteristics of the internal wavefield generated by tidal flow over uneven topography are investigated. It is found that "nontraditional effects'' profoundly change not only the dynamics of internal waves but also the rate at which the barotropic tidal energy is fed into the internal wavefield. Discarding the traditional approximation, internal waves are proved to be able to generate poleward of the critical latitude, rays of which are no longer symmetric and the limiting values of ray angles become greater or less than 90 degrees, depending on the local latitude and the direction of ray. More importantly, in contrast to the predictions of models based upon the traditional approximation, a substantial conversion occurs in the situations when stratification is so weak that the buoyancy frequency is below the tidal one.

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In this paper, we study the fission of a solitary wave in the stratified fluid with a free surface. It has been discovered that there is no difference between the fissions of the internal solitary waves in odd or even modes, and the effect of the stratification on the fission of a surface solitary wave can almost be neglected

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首先阐述了将渐变折射率薄膜细分为多层均匀薄膜的分层介质理论,接着给出了一种获得最佳分层数目的分层评价方法,最后以线性变化渐变折射率薄膜为例说明了如何优化获得渐变折射率薄膜的分层数目.研究发现:渐变折射率薄膜的分层数目与薄膜的厚度和薄膜的折射率变化快慢有关,在一定的折射率变化范围内,渐变折射率薄膜的分层数目随着薄膜厚度的增加先减小后增大.

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肉质小半灌木盐节木(Halocnemum strobilaceum)、里海盐爪爪(Kalidium capsicum)和盐爪爪(Kalidium foliatum)是中国西北盐生荒漠中分布的重要优势种植物。本文对生长在新疆盐漠环境中的三种植物种子的萌发生态学进行了研究。研究内容包括:(1)光照、温度对种子萌发的影响;(2)NaCl盐度对种子萌发和恢复、幼苗生长和恢复的影响;以及(3)低温层积处理对三种盐生植物种子休眠打破和耐盐性影响。 新成熟的盐节木、里海盐爪爪和盐爪爪种子都具有非深度生理休眠,它们分别需要经过4,4和8周的低温层积处理打破休眠。打破休眠的种子萌发的最适光温条件分别是25-30°C和光照(盐节木);15-30°C,光照或黑暗(里海盐爪爪);25°C和黑暗(盐爪爪)。 三种盐生植物的种子萌发对NaCl盐度胁迫有相似的响应,即低浓度不抑制萌发,高于一定浓度后,种子萌发随盐度的升高而逐渐降低,直至种子萌发被完全抑制。但是,开始抑制和完全抑制三种植物种子萌发的NaCl盐度是不同的。三种植物种子萌发受到抑制的起始浓度和种子萌发完全被抑制的盐度分别是:0.4和2.0 M(盐节木),0.2和0.6 M(里海盐爪爪),0.2和1.0 M(盐爪爪)。将未萌发的种子转入用蒸馏水饱和的滤纸上继续萌发,三种盐生植物的种子均有可恢复萌发的能力,经4.0 M NaCl处理后的种子,萌发恢复率都高于80%。三种植物的种子在蒸馏水中的总萌发率(在初始盐溶液中萌发的种子数与在蒸馏水中恢复萌发的种子数之和占所有供试种子数的百分率)高于各盐度条件下的种子总萌发率(在初始盐溶液中萌发的种子数与在蒸馏水中恢复萌发的种子数之和占所有供试种子数的百分率)。 盐节木和里海盐爪爪的种子萌发出的幼苗的早期生长对NaCl盐度胁迫有相似的响应,即随着盐度的升高,胚根的伸长逐渐降低;但是低盐度(≤0.4 M)不影响、甚至促进盐节木胚根的伸长,而各个盐度的NaCl均抑制里海盐爪爪的胚根伸长。盐节木的胚根生长较慢,在蒸馏水中培养24 h 后的根长< 1mm。低盐(0.2 M)促进胚根的伸长,但随盐度的继续升高(≥ 0.6 M),胚根伸长逐渐受到抑制,当盐度 ≥ 2.0 M NaCl时,盐节木胚根伸长完全停止。里海盐爪爪的胚根伸长快速,在蒸馏水中培养12 h后的平均根长为5 cm。低盐并不促进里海盐爪爪胚根的伸长,随盐度升高,胚根伸长逐渐受抑制。当盐度 ≥ 1.0 M NaCl时,里海盐爪爪的胚根伸长完全停止。但当转入蒸馏水中时,两种植物的胚根都可以继续伸长,伸长的能力随预处理盐溶液浓度的升高而降低,经 ≥ 4.0 M NaCl 预处理的盐节木胚根完全丧失继续伸长的能力;经0.6 M NaCl 预处理的里海盐爪爪胚根无法继续伸长。 低温层积处理对三种盐生植物的种子在NaCl溶液中的萌发均有显著促进作用。低温层积后,种子萌发可以发生的盐度范围提高;相同浓度NaCl溶液中,低温层积后的种子的萌发率和萌发速率都显著高于未经低温层积处理的种子。 实验结果表明三种盐生植物在种子萌发和早期幼苗生长阶段对盐生生境具有适应性。种子和幼苗早期在高盐分胁迫下保持的萌发恢复能力和胚根伸长生长的恢复能力是对盐生环境的特殊适应对策。这种适应对策有助于这三种植物在新疆的盐漠环境中得以成功的生存和繁衍。

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干旱区和半干旱区生长的植物具有复杂的生存机制,以确保其能够在特定的环境中生存和发展。植物在干旱的荒漠条件下的生存,与其特殊的种子萌发机制密切相关,这种机制能够确保植物在合适的时间与地点进行种子萌发与幼苗生长发育。在植物的生活史中,种子对极端环境具有最大的忍耐力,而萌发的幼苗对环境胁迫的忍耐程度最小。在干旱区生长的植物往往具有特殊的萌发机制使萌发出的幼苗能够度过对外界的敏感期,对于植物的生存具有重要意义。 毛乌素沙地是我国的四大沙地之一,该地区具有水分短缺,蒸发强烈,风沙剧烈和生境异质性高的特征。本文假设生长在这种极端环境中的植物也发展出了“适时适地”的种子萌发和幼苗生长的适应对策。为了验证以上的假设,本文选取毛乌素沙地不同生境中生长的两种优势固沙禾草——流动沙丘上生长的沙鞭(Psammochloa villosa)和固定沙丘上生长的赖草(Leymus secalinus)为研究材料,通过野外调查、温室控制实验和实验室控制实验的方法,从生理生态学的角度探讨这两种植物的种子萌发和幼苗生长过程对沙丘环境的适应对策,主要对比它们在种子休眠、萌发和幼苗早期生长过程中对沙丘生境适应性的异同点。研究结果表明: (1)新成熟的沙鞭和赖草的种子为适应冬季低温而发展出生理性的内生休眠——非深度生理休眠。沙鞭和赖草的种子分别需要经过4周和8周的低温层积处理(3-5ºC)来完全打破休眠。另外,划破种皮或者部分切除胚乳也能够促进种子的萌发,这进一步证明两种植物的种子具有非深度生理休眠。然而,切除胚乳在不同程度上影响它们的幼苗生长。由非深度生理休眠、温度和损伤种皮/胚乳调节的部分萌发机制能够确保两种植物的种子即使在条件适宜的情况下只有部分种子萌发,从而分散植物生存的风险性。 (2)毛乌素沙地的小量降水(无法触发萌发)使种子经常遭受湿润-干燥的交替胁迫过程。种子先在湿润条件下吸涨1d或者2d,然后在室温下干燥0-8天。尽管在经历反复吸涨和自然干燥脱水后仍能够保持萌发能力,沙鞭和赖草种子的萌发特性却发生了不同的变化:和各自的对照相比,沙鞭种子萌发率相同而萌发速率降低;赖草种子的萌发率和萌发速率都降低,部分种子进入休眠状态。沙鞭和赖草萌发出的幼苗可能由于没有后续降雨或者因沙蚀而遭受干燥胁迫,但是其幼苗在生长早期能够忍耐一定程度的干燥,再次湿润后部分幼苗能够恢复生长。沙鞭和赖草幼苗的耐干燥的“极限点”不同:当幼根长度为1 mm时,它们的幼苗忍耐干燥的时间分别是60d和30d;当幼根长度为4 mm时,它们的幼苗忍耐干燥的时间分别是14d和7d。沙鞭和赖草的种子和生长早期的幼苗的耐干燥性特性可能是它们对降雨量和降雨时间都不可预测的沙地生境的生存策略之一。 (3)不同的沙埋深度影响沙鞭和赖草的种子萌发和出苗。这两种植物的种子萌发和出苗都需1-2 cm的浅层沙埋。随着沙埋深度的增加,两种植物的种子萌发率和出苗率逐渐降低,强迫休眠率逐渐升高;萌发率与出苗率和沙埋深度呈负相关关系而休眠率和沙埋深度呈正相关关系。但是,沙鞭种子出苗的最大沙埋深度是8 cm,而赖草的则为4 cm。因强迫休眠而没有萌发的种子对维持一个长期的土壤种子库来说具有生态学优势,这些种子暴露在合适的萌发土壤深度时具有生长出幼苗的潜能。 (4)沙鞭和赖草的种子都具有大小的差异性,种子大小对沙鞭和赖草的种子在不同沙埋深度的出苗具有不同的影响。沙鞭的三种不同大小种子的平均质量分别为小,4.489 ± 0.012 mg (4 – 4.9 mg);中,5.457 ± 0.012 mg (5 – 5.9 mg)和大,6.415 ± 0.011 mg (6 – 6.9 mg)。赖草的两种不同大小种子的平均质量分别为小,3.083 ± 0.026 mg (3 – 3.5 mg)和大3.955 ± 0.028 mg (3.6 – 4.0 mg)。在相同的沙埋深度下,两种植物的大种子的出苗率都显著高于小种子。和小种子相比,两种植物的大种子由于贮藏更多的能量,所以在相同深度的沙埋中具有出苗率更高的生态优势,而大量小种子在沙埋中不能萌发,可以作为种子库保存在沙层中,这样就分散了一次性大量萌发给植物带来的冒险性。 (5)沙鞭和赖草的幼苗在生长过程中会遭受沙埋,其幼苗忍耐沙埋的能力与沙埋的相对深度(沙埋比例)和幼苗年龄有关。沙鞭和赖草幼苗的耐沙埋能力不同:沙鞭的2周龄幼苗可以忍耐达到株高100%的沙埋,而其1周龄幼苗只能忍耐75%的沙埋。赖草的1周龄和2周龄幼苗都只能忍耐75%的沙埋。沙埋之后,沙鞭和赖草幼苗的生物量,根/茎比以及根和茎的长度都受到不同程度的影响。赖草幼苗不能忍耐完全沙埋可能是限制它在流动沙丘上分布的一个原因。 (6)降雨量和降雨频率能够不同程度地影响沙鞭和赖草在不同沙层的萌发和出苗。这两种植物的种子萌发和出苗需要的最小降雨量不同:在一次浇水相当于5 mm降雨量后,沙鞭和赖草种子的萌发率都超过50%;但是使沙鞭和赖草的出苗率能够达到50%的降雨量分别为10 mm和15 mm。沙埋中的沙鞭和赖草种子的出苗对降雨的响应具有以下特征:两种植物种子的出苗随降雨量或者降雨频率的增加而增加;沙鞭的出苗率受到降雨量和降雨频率的显著影响,但是二者交互作用的影响不显著;赖草的出苗率受到降雨量、降雨频率以及二者交互作用的显著影响。 由非深度生理休眠,种子大小,干燥-湿润循环,沙埋和降雨调节的种子萌发和出苗机制确保了自然条件下沙鞭和赖草每次只有少量种子萌发和出苗,从而分散了两种植物在沙丘上的生存风险。 根据沙鞭和赖草在沙丘上的种子萌发和幼苗生长特性,本文为毛乌素沙地通过植物固沙恢复受损的沙地生态系统的种子飞播实践提出了几点建议。

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本文以中国极危种大花黄牡丹种子为研究材料,对其种子生物学、休眠与萌发特性进行研究,采用变温层积和激素处理解除种子休眠,并通过生物抑制物测试、胚培养、激素含量动态变化的测定,研究种子休眠的原因,从根本上解决了大花黄牡丹迁地保护过程中种子繁殖的技术难题,并初步探讨了大花黄牡丹致濒因素与种子休眠及萌发特性的关系,结果表明: 1.大花黄牡丹种子饱实度高,活力强,种皮较坚硬,但不存在吸水障碍,干燥条件下易因失水而丧失活力。迁地保护冷室中盆播18个月方可出苗,出苗率约4%;变温层积实验表明该种具有典型的下胚轴休眠和上胚轴生长抑制。 2.胚组织培养表明:带胚乳和种皮的胚不能萌发,剥除种皮和胚乳后,胚根可萌发,胚芽不生长,GA3处理上胚轴可促进生长,说明种皮和胚乳是导致大花黄牡丹种子下胚轴休眠的关键因素,而上胚轴生长抑制与胚本身关系更密切。 3.抑制物质提取实验表明:大花黄牡丹种子胚乳、种皮、胚等各部位的浸提液均存在抑制小白菜种子萌发的物质,且抑制作用依次增强,说明胚乳和胚是其下胚轴休眠的主要原因。经过暖层积(15 ℃/90 d)种子(未解除上胚轴生长抑制)的胚根、子叶、胚轴浸提液对小白菜和已解除休眠的大花黄牡丹种子的萌发均有不同程度的抑制作用,并依次减弱,说明种胚本身的抑制物质是导致生理休眠的主要原因。 4.变温层积处理和外源激素实验表明:新鲜种子采收后15 ℃暖层积3个月生根率可达85%,下胚轴休眠解除对温度要求严格,高于或低于15 ℃及变温条件均不利于下胚轴萌发;暖层积90d、根长大于6 cm种子再经过60~80 d/ 5 ℃冷层积,即可有效解除大花黄牡丹种子上胚轴的生长抑制,出芽率达80%,最终出苗率68%。不同浓度GA3及不同处理时间促进上胚轴伸长实验结果显示,GA3 400 mg/L浸种根长大于1.5 cm的种子2 h,出芽率可达100%,可以完全解除上胚轴的生长抑制作用。 5.休眠萌发过程中种子各部位内源激素含量动态变化分析结果说明,初始状态脱落酸含量高是导致大花黄牡丹种子下胚轴休眠、上胚轴生长抑制的主要原因之一,且上胚轴抑制与子叶、下胚轴和根的脱落酸含量密切相关;同时认为种子各部位初始生长素含量水平低是导致其休眠的另一个主要原因;变温层积过程中胚各部位脱落酸含量的急剧下降和生长素的迅速升高是解除休眠的关键;同时发现赤霉素在解除休眠和促进萌发过程中起着重要的促进作用,外源GA3能够有效地打破上胚轴的深度休眠。玉米素核苷在休眠与萌发进程中变化趋势与生长素和赤霉素相似,说明其对种子胚根和上胚轴的萌发和生长具有一定的促进作用。

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Mitochondrial disease currently received an increasing concern. However, the case-control design commonly adopted in this field is vulnerable to genetic background, population stratification and poor data quality. Although the phylogenetic analysis could

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以延河流域为例,采用环境梯度分层采样技术,对该流域种子植被的区系成分进行调查分析。结果表明,延河流域主要的种子植物区系共涉及57个科、148属、211种,其中裸子植物3科3属3种,被子植54科145属208种。从植物区系科属的分布型看,热带亚热带成分占31.57%,温带成分占28.07%;从属的分布型看,热带亚热带成分占11.72%,温带成分占60.54%。温带成分构成了本区系的主体,本区种子植物区系属温带性质。虽然数量上较整个黄土高原的植物区系成分较少,但这些物种却是该流域种子植物群落的主要构成种,对该区的生态恢复具有更重要的意义。在此基础上,进一步借助物种空间分布与环境要素响应图,分析211个物种分布的环境梯度空间,结果表明,它们可直接满足生态恢复重建的物种选择等需求,具有较好的应用价值。

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潜在植被的分布预测与制图对植被恢复规划具有重要的指导价值.利用广义相加模型(generalized additive model,GAM),结合GIS空间分析技术和环境梯度分层采样技术,为延河流域24个地带性物种建立了分布模型,并在考虑群落内部物种种间关系及其分布概率的基础上,对物种分布进行运算,模拟预测了延河流域37种植物群落的分布状况和延河流域的潜在植被分布.结果表明:研究区植被分布预测值与实际调查值间的差异不显著,预测的植被空间分布较好地反映了延河流域潜在的植被分布状况,表明该模型具有较好的预测能力,对于区域植被恢复的目标设定和恢复规划具有重要意义.

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繁殖更新是植物生活史的重要阶段,在退化生态系统中,植物繁殖更新能力往往较差,是植被恢复的限制环节,因而也成为恢复研究重点和核心。本研究选择岷江干旱河谷广泛分布的三种蔷薇:多苞蔷薇(R. multibracteata)、黄蔷薇(R. hugonis)和川滇蔷薇(R. soulieana)为研究对象,通过野外调查,在查明其生长、繁殖更新状况的基础上,采用控制和模拟实验,对种子和幼苗阶段进行了深入研究,综合分析更新潜力,并提出相对应的促进更新和植被恢复措施。主要结论如下: 1)三种蔷薇在岷江干旱河谷广泛分布,生长和繁殖状况良好,结实量大。各生长指标:株高、基径和冠幅,繁殖指标:结实数量、重量和单果重量都具有显著的空间差异性。基径对多苞蔷薇结实量影响最大;而冠幅对黄蔷薇结实量影响最大。海拔和纬度是对蔷薇生长和繁殖影响最大的环境因素,随着海拔和纬度的升高,植株生长更高大,结实量增加;坡度和坡向对其生长和繁殖也有一定影响,随着坡度 和坡向增加,蔷薇生长和结实受到抑制。 2)三种蔷薇在岷江干旱河谷更新现状不佳, 但更新潜力大。活力种子比率低,动物取食以及两年生幼苗的大量死亡是蔷薇更新的主要限制因素。多苞蔷薇和黄蔷薇的结实率低,川滇蔷薇较高。三种蔷薇种子产量大,但种子质量较差,更新具有充足的种源。三种蔷薇都能形成持久种子库,种子库中种子总量大,但有效种子少,黄蔷薇被动物啃食的比例很高,多苞蔷薇和川滇蔷薇也有一部分种子受到动物破坏。三种蔷薇幼苗库组成特征表现为,当年生幼苗所占比例很高,年龄较大幼苗所占比例小。 3)三种蔷薇都具有不同程度休眠,未经处理种子的发芽率极低。黄蔷薇休眠程度最深,为深度生理休眠;多苞蔷薇为中度生理休眠;川滇蔷薇为非深度生理休眠。三种蔷薇种子在形态上发育成熟,种皮具有透水性。蔷薇果果肉和瘦果中含有抑制物质,其浸泡液抑制了油菜种子萌发,果肉抑制作用更强,果肉和瘦果浸泡液的抑制程度分别为:川滇蔷薇>黄蔷薇>多苞蔷薇。切割和硫酸腐蚀提高了川滇蔷薇种子的发芽能力,而对多苞蔷薇和黄蔷薇没有影响。完全去除瘦果果皮和种皮提高了多苞蔷薇种子发芽率,但对黄蔷薇没有影响。赤霉素和烟水对蔷薇种子萌发没有促进作用。三种蔷薇打破休眠所需低温层积时间分别为:黄蔷薇>多苞蔷薇>川滇蔷薇。对于多苞蔷薇和川滇蔷薇,层积前对种子进行硫酸腐蚀或暖温层积能缩短低温层积时间,提高发芽率。对于多苞蔷薇,变温层积中暖温层积和低温层积具有一定的负补性,即延长暖温层积可以缩短种子萌发对低温层积的需要。 4)多苞蔷薇种子形态特征和种子休眠与萌发在不同海拔梯度间存在较大差异。种子采集时间、采集季节和干藏影响多苞蔷薇和川滇蔷薇的种子休眠。多苞蔷薇果实大小、种子大小和千粒重、种皮厚度随海拔升高而增加,而种子饱满率和活力随海拔升高而降低,种子休眠程度也随海拔升高而增加。种皮厚度与种子大小、千粒重成正相关关系,硫酸腐蚀后的种子经过不同时间的低温层积后,种子发芽率与种皮厚度、种子大小、千粒重、海拔成正相关关系。2006 年采集川滇蔷薇和多苞蔷薇种子休眠程度较2005 年低。种子休眠随种子年龄增加而减弱。高温和干旱能减轻多苞蔷薇和川滇蔷薇种子休眠。 5)三种蔷薇的生长和生物量积累在干旱胁迫条件下受到抑制,而生物量分配、叶片形态特征和水分利用特征等都发生了变化。三种蔷薇的根、茎、叶各器官生物量以及总生物量等在干旱胁迫下明显减小,叶片脱落数量增加。在干旱胁迫条件下,较多的生物量分配到地下部分,从而这使R/S 明显增加。比叶面积(SLA)和冠层面积比(LAR)对干旱胁迫的反应不敏感,仅有部分物种在干旱胁迫条件下发生了变化,并且其变化特点在不同年龄幼苗之间有一定差异。干旱胁迫对WUE 的影响在不同物种间存在差异。多苞蔷薇和黄蔷薇的WUE 随着干旱胁迫的增加而增大, 而川滇蔷薇的WUE 则随干旱胁迫增加而减小。在干旱胁迫条件下,多苞蔷薇和黄蔷薇叶片脱落量和生物量减小幅度较川滇蔷薇大,表明其抗旱能力较强。在干旱胁迫条件,三种蔷薇两年生幼苗的生物量减小幅度较当年生幼苗小,表明两年生幼苗的抗旱能力更强。 6)两种植被恢复措施中,幼苗移栽比播种具有更好的植被恢复效果。播种后,蔷薇种子的发芽率较高,但出苗率都很低,即使出苗,幼苗也几乎在一月内全部死亡。 三种微生境条件下(灌木、半灌木和裸地),种子出苗和幼苗成活没有差异。移栽幼苗总体死亡率都比较低,小于20%。特别是两年生幼苗死亡率更低,小于2%。移栽后的幼苗生长状况良好,在整个生长季中,各生长指标不断增加。生境对幼苗的存活率没有显著影响,但对于幼苗的生长和生物量积累有一定影响,裸地更有利于幼苗生长和生物量积累。与当年生幼苗相比,两年生幼苗具有更高的成活率。总之,三种蔷薇在干旱河谷分布广泛、生长繁殖状况良好,结实量大,具有丰富种源,繁殖更新潜力大,但繁殖更新状况不佳;种子散布后动物对种子的取食、种子的深度休眠过程、种子出苗以及当年生幼苗的存活和定居是更新的主要限制环节。水分是影响结实、种子休眠解除和萌发,幼苗存活和定居的最主要的限制因素。在植被恢复中,应在种子成熟季节大量采集种子,在室内打破休眠后进行人工播种,培育两年生幼苗,通过幼苗移栽方式进行植被恢复。川滇蔷薇应栽种在相对湿润的过渡区,而多苞蔷薇和黄蔷薇可以应用于核心区植被恢复。 Regeneration is an important phase in plant life cycle. It has been a key component of ecological restoration in degradation ecosystem in which plants commonly has poor regeneration. In this paper, we investigated the natural growth, propagation and regeneration status of native three rose species, Rosa multibracteata, R. hugonis and R. soulieana, and analysis the limitation in seed germination and seedling establishment stages. Advice on facilitating the use of these plants in restoration based on the results has been proposed. The results were as follows: 1) Three rose plants widely distributed in the dry valley of the Minjiang River, and made a good performance in growth and propagation. There were significant spatial differences in each growth parameter, such as ramet height, basal diameter, crown diameter and propagation parameters including hip number of a clump, hip mass of a clump and a hip mass. Basa diameter was the most important growth parameter influencing fruit number for R. multibracteata and crown diameter was for R. hugoni. Altitude and latitude had the greatest effect on the growth and propagation of rose plants among environmental conditions. Each parameter of growth and propagation increased with the increase of altitude and latitude. In addition, the increase of slope and aspect limited the growth and propagation. 2) Three rose plants had poor natural regeneration, but great regeneration potential. Low seed viability, predation and higher mortality of current year old seedlings were the limitation in regeneration. R. multibracteata and R. hugonis had higher fruiting rates than R. souliean. All three plants produced a great number of seeds, while their viability was poor. Three rose plants had persistent seed banks, with high total seed number but very low viable seed density. Predation was most severe in R. hugonis, and it also existed to some degree in R. multibracteata and R. soulieana. The seedling age-structure was characteristic of current-year seedlings predominating and few older seedlings were observed. 3) Three rose seeds were dormant and untreated seeds germinated with very low germination percentages. The rose seeds had morphological mature embryos, and achenes were permeable. Some inhabit substances existed in hips and achenes for the extracts of hips and achenes inhibited germination of Brassica campestris. The inhibition effect of the extracts of three rose hip and achenes was R. soulieana>R. hugonis>R. multibracteata. Mechanical and H2SO4 scarification increased R. soulieana germination but had no effect on germination of R. hugonis and R. multibracteata seeds. Full removal of pericarp and testa improved the germination of R. multibracteata but did not affect R. hugonis germination. GA3 and smoke water had no positive effect on rose seed germination. The periods of cold stratification required to released seed dormancy was R. hugonis > R. soulieana >R. multibracteata. H2SO4 scarification and warm stratification shortened cold stratification to release dormancy for R. soulieana and R. multibracteata. Warm stratification had complementary effect for cold stratification, i.e. the longer warm stratification seeds received, the shorter cold stratification were required to obtain the same germination percentage. Three rose seeds had different kinds of dormancy; R. hugonis has deep physiological dormancy, R. multibracteata with intermediate physiological dormancy and R. souliean non-deep physiological dormancy. 4)The seeds traits and dormancy of R. multibracteata showed significant difference across altitudes. Year and season of seed collection had significant effect on seed dormancy for both R. souliean and R. multibracteata. Hip size, seed size, seed weight, seed coat thickness and seed dormancy level increased with the increase of the altitude. There were positive relations between seed coat thickness with seed size and seed weight. Germination percentage of seeds treated with H2SO4 scarification following different periods of cold stratification showed positive relation with seed coat thickness, seed size, seed weight and altitude. Seeds of R. souliean and R. multibracteata collected in 2006 had low dormancy level than those collected in 2005. Seed dormancy decreased with increasing seeds age. High temperature and drought were associated with low dormancy level. 5) Seedling growth, the total dry mass and their components of seedlings were reduced, while leaf senescence accelerated under drought stress. More biomass allocation to root system resulted in higher R/S ratio under drought. Water-use efficiency (WUE) of R. multibracteata and R. hugonis increased, while it declined for R. soulieana under drought stress. R. soulieana seedlings had poor drought-resistance capacity it had more senescent leaves, and its reduction of biomass was stronger than two other rose plants under drought. The reduction degree of one year old seedlings under drought stress was slighter than that of current year seedlings. Therefore, one year old seedling was more drought-resistent compared to current year seedlings. 6)Planting seedlings may have better effect in comparison with direct seeding. Most seeds germinated after seeding, but seedling emergence was very low. More than 80 % seedlings from direct seeding died within a months after emergence. Seedling emergence and survival rate did not show difference among microhabitats. Mortality rates of seedlings artificially planted in microhabitats were general lower than 20 %, and the mortality rate of one year old seedlings was lower than 2 %. Each grow parameter including plant height, leaf number and branch number continually increased after planting. Microhabitat type had effect on the growth parameter and biomass production, but it did not influence the seedling survival. Bare land tended to facilitate seedling growth. One year old seedlings had higher survival rate than current year seedlings. In conculsion, the three rose had wide distribution in the dry valley of the Minjiang River. They produced many seeds and had tolerance to drought stress to some degree. But they had poor regeneration in habitats may be caused by predation, seed dormancy,and high mortality in current year seedlings. We recommend that rose plants should be utilized in restoration by planting two-year old seedlings in spring. A large quantity of seeds should be collected artificially in autumn, release seed dormancy in room, and then cultivate two-year old seedlings by seeding in particular container. R. soulieana seedling probably be planted in transition area, and R. multibracteata and R. hugonis can be used in core area of the dry valley of the Minjiang River.