苔癣植物适应孢子传播的结构

本文论述了苔癣植物的真蒴柄、假蒴柄、生殖托柄、孢蒴表皮、蒴齿和弹丝等适应孢子传播的形态、结构和功能。     

水位与光强变化对尖叶泥炭藓孢蒴生产动态的影响

选取尖叶泥炭藓(Sphagnum capillifolium)为试验材料, 在模拟水位与光强条件下, 对人工构建的苔藓植物群落进行室内培养, 每隔1-3天观察并记录植株高度、孢蒴变化过程及变化时间, 分析了不同水位与光强条件对孢蒴生产的植物功能属性动态的影响。水位上升促进了蒴柄伸长及植株高增长, 增加了孢蒴开裂率及遮蔽率。光强增加有助于孢蒴生长, 并提高了孢蒴开裂率。在孢蒴直径以及植株高增长性状上, 水位与光强存在交互作用。水位与光强对孢蒴增长率均没有影响。此外, 水位升高与光强增加使孢蒴成熟及蒴柄伸长时间提前, 总体上使孢子释放时间分别提前了4.0 d和4.8 d, 由此可能减小了孢子体因受夏季干旱影响而败育的风险。孢子释放后, 繁殖株高增长加速, 可为未来的再次繁殖奠定基础。     

Effects of water level and light intensity on capsule production dynamics of Sphagnum capillifolium

 选取尖叶泥炭藓(Sphagnum capillifolium)为试验材料, 在模拟水位与光强条件下, 对人工构建的苔藓植物群落进行室内培养, 每隔1-3天观察并记录植株高度、孢蒴变化过程及变化时间, 分析了不同水位与光强条件对孢蒴生产的植物功能属性动态的影响。水位上升促进了蒴柄伸长及植株高增长, 增加了孢蒴开裂率及遮蔽率。光强增加有助于孢蒴生长, 并提高了孢蒴开裂率。在孢蒴直径以及植株高增长性状上, 水位与光强存在交互作用。水位与光强对孢蒴增长率均没有影响。此外, 水位升高与光强增加使孢蒴成熟及蒴柄伸长时间提前, 总体上使孢子释放时间分别提前了4.0 d和4.8 d, 由此可能减小了孢子体因受夏季干旱影响而败育的风险。孢子释放后, 繁殖株高增长加速, 可为未来的再次繁殖奠定基础。     

苔藓植物孢子形态的研究(一)——几种泥炭藓(Sphagnum)孢子的光学研究和电子显微镜观察

泥炭藓(Sphagnum)是水湿或沼泽地区丛生藓类。其植物体形态和构造分化简单,孢子体仅具由配子体组织发育的假蒴柄;孢蒴球形,盖裂,无蒴轴及蒴齿分化,因而为鲜纲中一个独立的亚纲,在苔藓系统排列中,列为原始的类型之一。     

乌兰坝紫萼藓(紫萼藓科)成熟孢子体的发现（英文）

最近在中国内蒙古发现了乌兰坝紫萼藓(Grimmia ulaandamana J. Mu?oz, C. Feng, X.L. Bai&J. Kou)的可育植株,介绍了乌兰坝紫萼藓成熟孢子体、雌株和雄株的特征。孢子体的孢蒴长于蒴柄,蒴柄弯曲,蒴壶表面具纵褶,蒴壁中部表皮细胞厚壁,环带细胞方形或短长方形,蒴盖有喙;蒴齿具疣并在上部分叉,蒴齿在基部分开,蒴齿基部低于蒴壶口,蒴壁表皮细胞和蒴齿之间存在一层小型细胞,蒴齿骨小梁在基部1/3处强烈凸出;蒴帽基部完整。最内侧雌苞叶较茎叶大。乌兰坝紫萼藓具有重要的形态特征变异,可育植株与相似种直叶紫萼藓(G. elatior)易于区分。对乌兰坝紫萼藓进行了全面的描述并配显微图,探讨了孢子体对确定其系统发育位置的重要性。     

中国藓类植物新记录属—筛齿藓属

作者在芬兰赫尔辛基大学植物标本馆(H)研究Dr.T.Koponen 1970年在台湾采集的部份苔藓标本时,发现了筛齿藓(Coscinodon cribrosus (Hedw.) Spruce)。筛齿藓属(Coscinodon Spreng)为中国植物新记录属,特此报道。筛齿藓的主要区别特征为:(1)植物体矮小,呈丛生垫状,叶先端具透明毛尖;(2)叶披针形,中肋两侧具明显长纵褶;(3)叶基部细胞长形至长方形,薄壁;(4)蒴柄短,孢蒴内隐于孢叶之中;(5)蒴帽大,钟形,具纵褶,覆盖大部孢蒴;(6)蒴齿具筛孔。     

中国新记录——毛齿藓短蒴变种(新拟)

该研究首次报道了毛齿藓短蒴变种(新拟)在中国的分布和毛齿藓属在新疆的分布。研究表明：(1)毛齿藓短蒴变种的主要识别特征为：叶基部鞘状,突然狭窄成线状披针形,背仰,叶缘平展,中肋充满叶上部,背面粗糙,远轴面有厚壁细胞束分化,叶细胞长方形至短长方形;有假根生芽胞;孢蒴椭球形,稍弓形弯曲,蒴齿线状披针形,二裂至近基部。(2)毛齿藓属的3个分类单位在中国均有分布,毛齿藓短蒴变种以较短的孢蒴和蒴柄区别于原变种,以有根生芽胞、叶基部呈明显鞘状、叶缘平展区别于云南毛齿藓的无假根生芽胞、叶基部略呈鞘状、叶缘背卷。(3)在牛毛藓科中有许多类群与毛齿藓短蒴变种形态相似,但仅有毛齿藓属的叶在横切面上主细胞的远轴面有厚壁细胞束,而其他类群的叶在横切上主细胞的近轴面和远轴面均有厚壁细胞束。该变种的叶背仰不同于牛毛藓科其他属的叶直立;以具鞘部的叶、表面光滑的孢蒴、内弯的蒴齿区别于无鞘部的叶、表面有纵沟槽的孢蒴、直立的蒴齿的牛毛藓属。(4)该变种属北极 高山分布类型,表现出了明显的欧洲 亚洲 北美洲间断分布模式,可作为研究气候变化、海陆变迁的重要材料。     

角苔孢蒴发育的显微观察

对角苔科(Anthocerotaceae)角苔(Anthoceros punctatus)孢蒴的形态和发育进行显微观察。通过观察发现,角苔孢蒴在开裂带处有2列特殊的表皮细胞分布,开裂带下方的细胞扁小且排列紧密,蒴壁最内层细胞在孢蒴发育后期其内切向壁和径向壁强烈加厚,弹丝细胞具明显加厚的壁,角苔孢蒴的上述结构特征都有利于孢子的散发。同时,在角苔孢子体上观察到了与苔类和藓类不同的独特特征。     

葫芦藓原丝体的采集和观察

初中植物学苔蘚植物类这一节,要讲到葫芦蘚。采集葫芦蘚的茎叶、蒴柄、孢蒴的观察是很容易的,但采集和观察它的原絲体就较为困难一些,因为原絲体是长在土壤表层,体很微小,肉眼不易区別它。但在教学中,让学生对原絲体进行观察,对认识苔蘚植物跟藻类植物系统发生的联系,是非常有必要的。现将原絲体的采集和观察方法叙述如下。     

烟气对泥炭藓孢子萌发影响的模拟研究

适量烟气能促进种子萌发,但对苔藓植物孢子的作用尚不清楚.选取采自长白山区泥炭地的粗叶泥炭藓和中位泥炭藓的孢蒴为试验材料,通过燃烧泥炭地植物产生烟气,制备烟溶液,分别与不同大小(大:直径为2.10～2.50 mm;小:直径为1.50～1.90 mm)以及不同保存时长(旧:4.3和6.3年;新:0.3年)的孢蒴进行两组双因素试验,经不同时长的烟溶液浸泡和萌发试验,模拟研究烟气、孢蒴大小和保存时长对苔藓植物孢子萌发的影响.结果表明: 烟溶液浸泡影响孢子萌发,培养10 d时,不同时长的烟溶液浸泡均可使孢子的萌发率提高5倍以上,小孢蒴孢子的萌发率高;培养21 d时,仅适度浸泡(3 d)表现出促进萌发的作用,孢蒴大小对孢子萌发率无影响;烟溶液浸泡对长时间保存(4.3和6.3年)的孢蒴孢子萌发无促进作用.研究表明,适量烟气可加速新泥炭藓孢子以及小孢蒴孢子的萌发.在存在不定期火烧干扰的泥炭地中,与对种子植物的作用类似,烟气可能在苔藓植物种群的有性更新和种群维持中发挥重要作用.     

Design and Mechanics Simulation of Bionic Lubrication System of Artificial Joints

We propose a new structure for artificial joints with a joint capsule which is designed to overcome the drawback of current prostheses that omit many functions of the lubricant and the joint capsule. The new structure is composed of three components： lubricant, artificial joint and artificial joint capsule. The lubricant sealed in the capsule can not only reduce the wear of the artificial joint but also prevents the wear particles leaking into the body. So unexpected reactions between the wear particles and body can be avoided completely. A three-dimensional （3-D） finite element analysis （FEA） model was created for a bionic knee joint with capsule. The stresses and their distribution in the artificial capsule were simulated with different thickness, loadings, and flexion angles. The results show that the maximum stress occurs in the area between the artificial joint and the capsule. The effects of capsule thickness and the angles of flexion on stress are discussed in detail.     

Genetic organization of the Escherichia coli K10 capsule gene cluster: identification and characterization of two conserved regions in group III capsule gene clusters encoding polysaccharide transport functions

Analysis of the Escherichia coli K10 capsule gene cluster identified two regions, regions 1 and 3, conserved between different group III capsule gene clusters. Region 1 encodes homologues of KpsD, KpsM, KpsT, and KpsE proteins, and region 3 encodes homologues of the KpsC and KpsS proteins. An rfaH mutation abolished K10 capsule production, suggesting that expression of the K10 capsule was regulated by RfaH in a manner analogous to group II capsule gene clusters. An IS3 element and a phiR73-like prophage, both of which may have played a role in the acquisition of group III capsule gene clusters, were detected flanking the K10 capsule genes.     

The capsule biosynthetic locus of Pasteurella multocida A:1

Pasteurella multocida is the aetiological agent of fowl cholera, bovine haemorrhagic septicaemia and atrophie rhinitis in pigs. Many strains of P. multocida express a capsule on their surface. However, nothing is known about the capsule biosynthetic locus in P. multocida although the capsule has been implicated as a virulence factor. The entire capsule locus of P. multocida A:1 was cloned and sequenced. The locus is divided into three regions. Region 1 comprises four ORFs which are involved in the transport of the capsule polysaccharide to the surface. Region 2 comprises five ORFs whose postulated protein products are involved in the biosynthesis of the polysaccharide capsule. Region 3 comprises two ORFs whose postulated products show similarity to proteins that are involved in the phospholipid substitution of the polysaccharide capsule.     

Isolation and characterization of capsule structure mutant strains of Cryptococcus neoformans

The capsule of Cryptococcus neoformans is the most obvious virulence factor of this pathogenic yeast. The main capsule constituents are glucuronoxylomannans (GXM). Although several studies have focused on GXM composition and structure, very little is known about their genetics. To elucidate the relationship between the capsule structure and the pathophysiology of the cryptococcosis, genetic screening for mutant strains producing a structurally modified capsule was set up. Using monoclonal antibodies specific for different capsule sugar epitopes, we isolated strains with different mutated capsule structures (Cas mutants). According to their reactivities with various monoclonal antibodies, the mutants were classified into six groups (Cas1 to Cas6). One Cas2 mutant was used to clone the corresponding gene by complementation. This gene (USX1) encodes the previously identified UDP-xylose synthase. We demonstrated that it is necessary for both capsule xylosylation and C. neoformans virulence.     

The volume and hydration of the Cryptococcus neoformans polysaccharide capsule

We present a new method to measure capsule size in the human fungal pathogen Cryptococcus neoformans that avoids the limitations and biases inherent in India ink measurements. The method is based on the use of gamma-radiation, which efficiently releases the capsule from the cell. By comparing the volume of irradiated and non-irradiated cells, one can accurately estimate the relative size of the capsule per cell. This method was also used to obtain an estimate of the capsule weight and water content. The C. neoformans capsule is a highly hydrated structure in all the conditions measured. However, after capsule enlargement, the amount of capsular polysaccharide significantly increases, suggesting a that capsule growth has a high energy cost for the cell.     

Spatial and temporal sequence of capsule construction in Cryptococcus neoformans

The pathogenic yeast Cryptococcus neoformans is distinguished by an extensive polysaccharide capsule, which impedes host defences and is absolutely required for fungal virulence. Despite the biological importance of the capsule, nothing is known about how it is assembled. Substantial capsule growth occurs in two distinct situations relevant to cryptococcal pathogenesis: formation of new buds and induction of capsule on mature cells. We developed pulse-chase protocols to examine these events in a dynamic way using a variety of microscopy techniques. We show that the capsule overlying buds is newly synthesized and differs physically from the corresponding parental material. New capsule formed by mature cells upon induction of synthesis is added at the inner aspect of the existing structure, displacing pre-existing material outwards. Surprisingly, new polysaccharide material is also deposited throughout the capsule, yielding a progressively denser structure. These results yield the first model of capsule synthesis and open new lines of investigation into the underlying mechanisms.     

Effect of 2-chloroethylphosphonic acid on capsule formation and alkaloid content in Papaver somniferum

Application of different concentrations of ethephon (2-chloroethylphosphonic acid) to Papaver somniferum L. at the times of stem elongation, bud, and capsule formation produced different effects. Ethephon (10^-2 M ) retarded growth of the plant and inhibited capsule formation during stem elongation, significantly reduced capsule size during the flowering period, but did not alter capsule development during capsule formation. When applied during the period of stem elongation, ethephon (10^-3 M and 10^-4 M ) reduced capsule size; alkaloid accumulation was reduced by ethephon at a concentration of 10^-3 M , but slightly increased by 10^-4 M . Ethephon (10^-3 M and 10^-4 M ) did not alter capsule development or alkaloid content significantly when applied during bud formation, but stimulated capsule size and alkaloid content when applied during capsule formation. Pretreating the plants with Ag⁺ (silver nitrate) did not reverse the ethephon effect. The results suggest that capsule maturation and alkaloid accumulation in P. somniferum are modified by ethylene, which is produced as a result of exogenous ethephon treatment.     

Radiological studies reveal radial differences in the architecture of the polysaccharide capsule of Cryptococcus neoformans

The polysaccharide capsule of the pathogenic fungus Cryptococcus neoformans is an important virulence factor, but relatively little is known about its architecture. We applied a combination of radiological, chemical, and serological methods to investigate the structure of this polysaccharide capsule. Exposure of C. neoformans cells to gamma radiation, dimethyl sulfoxide, or radiolabeled monoclonal antibody removed a significant part of the capsule. Short intervals of gamma irradiation removed the outer portion of the cryptococcal capsule without killing cells, which could subsequently repair their capsules. Survival analysis of irradiated wild-type, acapsular mutant, and complemented mutant strains demonstrated that the capsule contributed to radioprotection and had a linear attenuation coefficient higher than that of lead. The capsule portions remaining after dimethyl sulfoxide or gamma radiation treatment were comparable in size, 65 to 66 microm3, and retained immunoreactivity for a monoclonal antibody to glucuronoxylomannan. Simultaneous or sequential treatment of the cells with dimethyl sulfoxide and radiation removed the remaining capsule so that it was not visible by light microscopy. The capsule could be protected against radiation by either of the free radical scavengers ascorbic acid and sorbitol. Sugar composition analysis of polysaccharide removed from the outer and inner parts of the capsule revealed significant differences in glucuronic acid and xylose molar ratios, implying differences in the chemical structure of the constituent polysaccharides. Our results provide compelling evidence for the existence of two zones in the C. neoformans capsule that differ in susceptibility to dimethyl sulfoxide and radiation and, possibly, in packing and composition.