领春木茎次生木质部中导管穿孔板的变异

领春木Euptelea pleiosperma Hook. f. &; Thoms.隶属领春木科Eupteleaceae。该科为东亚特有的单型科,其系统位置一直颇有争议。本文对中国产领春木茎次生木质部中导管穿孔板的变异进行了观察,以期为它的系统位置提供进一步的解剖学证据。结果表明,领春木茎次生木质部中包括无明显穿孔板的管胞状导管和典型的导管两种类型。在无明显穿孔板的导管中,穿孔中的纹孔膜全部或部分消失,但穿孔无规则排列或聚集,不形成具典型的形态特征的穿孔板;在典型的导管中,穿孔板形态变异较大,包括几个类型:网状穿孔板(含麻黄式穿孔板)、网状和梯状混合型穿孔板、梯状穿孔板、梯状穿孔板向单穿孔板的过渡。在上述导管穿孔板类型中,只有梯状穿孔板的穿孔中可以观察到纹孔膜的残余。在领春木次生木质部中也观察到了端壁多穿孔板及侧壁穿孔板。根据观察结果,我们认为领春木次生木质部导管穿孔板的许多特征说明该科可能处于毛茛目中比较原始的系统位置。     

黄三七(毛茛科)茎次生木质部导管穿孔板的研究

利用扫描电子显微镜对东亚特有植物黄三七（Souliea vaginata（Maxim.） Franch.）茎的次生木质部离析材料进行了观察,结果表明,黄三七茎次生木质部中的导管分子端壁上具网状穿孔板（麻黄式穿孔板）、梯状穿孔板、网状-梯状混合穿孔板、网状-梯状-单穿孔混合型穿孔板、梯状-单穿孔混合型穿孔板及单穿孔板,同时也观察到了端壁多穿孔板和侧壁穿孔板,并对不同类型穿孔板中纹孔膜的残留也进行了观察。其中,网状穿孔板、各种过渡类型的穿孔板均为毛茛科植物中首次报道。根据观察结果,对导管分子穿孔板的演化及黄三七属植物的系统位置进行了分析。     

维管植物导管及其穿孔板的研究进展

介绍了导管及其穿孔板的研究进展,包括导管的特征(穿孔板的类型、多穿孔板与侧壁穿孔板、纹孔膜残留),导管的起源与穿孔板的演化,蕨类植物、裸子植物与被子植物导管的比较,并就导管进化与穿孔板演化．导管的二型性现象、侧壁穿孔板、多穿孔板与穿孔中纹孔膜．生态对导管进化的影响等方面以及对今后的研究作了展望。     

昆栏树属、水青树属和领春木属花粉形态的研究

昆栏树属(Trochodendron)、水青树属(Tetracentron)和领春木属(Euptelea)是一群 种数少而较原始的被子植物。它们主要分布于我国。 对于它们的系统位置存在着不同的看 法。因此本研究的目的,一方面为讨论系统位置时提供孢粉学的资料,另一方面也可为鉴定化 石花粉提供依据。 从花粉形态看,支持这三个属分别成立三个科。昆栏树属和水青树属花粉具三沟,而木兰科为单槽类型,因此不同意把它们放在木兰科(或目)。领春木属花粉具皱(rugate),皱膜上具粗颗粒(短条),如果皱进一步缩短和增加数目,类似于金缕梅科某些属,因此支持ronquist (1968)把领春木科放在金缕梅目。Hutchinson(1969)把昆栏树属和领春木属放在同一科(昆栏树科),从形态结构,导管存在与否,染色体数目,这两属差异较大,同时花粉的形态差别也较大,本文不支持这种观点。     

黄三七( 毛茛科) 茎次生木质部导管穿孔板的研究*

利用扫描电子显微镜对东亚特有植物黄三七( Souliea vaginata (Maxim. ) Franch. ) 茎的次生木质部
离析材料进行了观察, 结果表明, 黄三七茎次生木质部中的导管分子端壁上具网状穿孔板( 麻黄式穿孔
板) 、梯状穿孔板、网状- 梯状混合穿孔板、网状- 梯状- 单穿孔混合型穿孔板、梯状- 单穿孔混合型穿
孔板及单穿孔板, 同时也观察到了端壁多穿孔板和侧壁穿孔板, 并对不同类型穿孔板中纹孔膜的残留也进
行了观察。其中, 网状穿孔板、各种过渡类型的穿孔板均为毛茛科植物中首次报道。根据观察结果, 对导
管分子穿孔板的演化及黄三七属植物的系统位置进行了分析。     

阳桃次生木质部导管分子及侵填体的研究

运用细胞图象分析系统和显微照相的方法对阳桃次生木质部导管分子进行了观察研究。次生木质部导管分子类型有两端具尾导管、一端具尾导管和无尾导管。导管分子穿孔板存在着2种类型:两端均为一个单穿孔板;一端为一个单穿孔板,另一端为具两个单穿孔的复穿孔板。48%的导管分子具有囊状侵填体;管间纹孔式为互列纹孔式。     

余甘子次生木质部导管分子观察研究

运用细胞图象分析系统及显微照相的方法,对余甘子次生木质部导管分子进行观察研究.结果发现,余甘子次生木质部导管分子中存在着许多不同的样式,导管分子大多数具尾;其穿孔板存在着两种类型:(1)两端均为1个单穿孔板;(2)一端为1个单穿孔板另一端为2个单穿孔板;(3)极少数的导管分子具有特殊的内含物;(4)管间纹孔式为互列纹孔式;(5)导管射线间纹孔式为混合型纹孔与横列刻痕状纹孔以及梯状穿孔.     

类叶升麻(毛茛科)次生木质部管状分子的研究

利用扫描电子显微镜对毛良科类叶升麻（Artaea asiaticaHara）根和根状茎次生木质部中的管状分子进行观察．发观其管状分子类型丰富,主要有：管胞、管胞状导管、纤维导管和典型的导管分子,其中管胞、管胞状导管和纤维导管为在该类群中首次报道;在导管分子中．存在着梯状穿孔板、网状穿孔板、混合型穿孔板和单穿孔板．其中网状穿孔板和混合型穿孔板为在陔类群中的首次报道;对其导管分子上的侧壁穿孔板、多穿孔板和纹孔膜残余也进行了描述。根据类叶升麻次生木质部中多变的管状分子类型,认为以往积累的有关毛茛科植物管状分子类型及导管穿孔板类型是小个面的,因此以该性状为参考作出的有关某一个类群的原始性和进化性的推论也是不可靠的。同时探讨了不同类型管状分子作类叶升麻不同器官的分布与其生理功能和生态环境的关系,同时将该植物作为毛莨科的代表类群．与其它基邴类群植物导管分子进行了比较。     

木通科4属植物导管穿孔板的比较研究

运用扫描电子显微镜法(SEM)对木通科(Lardizabalaceae)4属植物茎的次生木质部导管分子进行观察,结果表明:(1)端壁均具有单穿孔板;(2)串果藤属的导管分子具有丰富的穿孔板类型,包括网状、梯状、单穿孔及过渡类型,穿孔具有网状、丝状、片状的纹孔膜残余;大血藤属和八月瓜属的导管分子具有相似的特征,端壁具有梯状、单穿孔及梯—单混合穿孔板;野木瓜属只具有单穿孔板;(3)侧壁上具有穿孔板,多为梯状或梯—网混合类型(除了野木瓜属);(4)野木瓜属的导管侧壁具有独特的螺旋状加厚。各属导管的不同特征为木通科的系统演化提供比较可靠的依据。     

领春木的染色体数目及配子体的发育

本文报道了领春木属的一个国产种Euptelea pleiospermum Hook.f.et Thoms的染色体数目,n=14,2n=28。描述了它的胚珠结构,大小孢子的发育及胚囊的类型。     

The effect of SEM preparation on pit membrane remnants in vessel element end-walls of primitive angiosperms

Scanning electron microscope (SEM) is necessary to demonstrate presence or absence of pit membranes in possible perforations or the type of pit membrane remnants in perforations in vessel element end-walls of angiosperms, but it was unconfirmed and questionable whether pit membrane absence in pits was affected by the processing and handling before SEM observations. To solve this question, the secondary xylem of four woody species from primitive angiosperms, Illicium henryi Diels. (Illiciaceae), Schisandra rubriflora (Franch.) Rehd. et Wils. (Schisandraceae), Tetracentron sinensis Oliv. and Trochodendron aralioides Sieb. & Zucc. (Trochodendraceae) was chosen and the following techniques were used: (1) fresh materials were examined in low-vacuum with ESEM. (2) Air-dried materials were examined both in low- and high-vacuum with ESEM. (3) Fresh materials fixed in several different fixatives were observed in low-vacuum, respectively. (4) Smooth surface of the material by paraffin section methods was examined in high-vacuum. (5) Materials treated by Jeffrey's Fluid were observed in high-vacuum.Pit membranes and remnants in perforations of fresh material were little different from that of treated materials. Absence of the pit membrane in perforations (pits) in the end-wall was not attributed to the processing and handling. Information of pit membranes and remnants in perforations in end-wall based on the SEM observation might be validly claimed.     

Origin and nature of vessels in monocotyledons. 5. Araceae subfamily Colocasioideae

Tracheary elements from macerations of roots and stems of one species each of five genera of Araceae subfamily Colocasioideae were studied by means of SEM (scanning electron microscopy). All of the genera have vessel elements not merely in roots, as previously reported for the family as a whole, but also in stems. The vessel elements of stems in all genera other than Syngonium are less specialized than those of roots; stem vessel elements are tracheid-like and have porose pit membrane remnants in perforations. The perforations with pit membrane remnants demonstrate probable early stages in evolution of vessels from tracheids in primary xylem of monocotyledons. The vessel elements with such incipient perforation plates lack differentiation in secondary wall thickenings between perforation plate and lateral wall, and such vessel elements cannot be identified with any reliability by means of light microscopy. The discrepancy in specialization between root and stem vessel elements in genera other than Syngonium is ascribed to probable high conductive rates in roots where soil moisture fluctuates markedly, in contrast with the storage nature of stems, in which selective value for rapid conduction is less. Syngonium stem vessels are considered adapted for rapid conduction because the stems in that genus are scandent. Correlation between vessel element morphology and ecology and habit are supported. Although large porosities in vessel elements facilitate conduction, smaller porosities may merely represent rudimentary pit membrane lysis.     

The anatomy of lotus fibers found in petioles of Nelumbo nucifera

Lotus fibers are the isolated helical secondary cell wall thickenings from tracheary elements of lotus (Nelumbo nucifera Gaertn) petioles. In this study the anatomical characteristics of lotus petioles and microstructures of tracheary elements were studied using light microscopy (LM) and scanning electron microscopy (SEM). The results show that vascular bundles of lotus petioles are scattered throughout ground tissue. Their tracheary elements are of various sizes and there are several patterns of secondary wall thickening present. However, only secondary thickening in a ribbon-like helical pattern can be drawn out from the petiole to form lotus fibers for subsequent utilization. Study of the microstructure of the tracheary elements reveals that there are two pit structures present in the end walls in addition to pits with intact pit membranes: those with porose or web-like remnants pit membrane and those that lack pit membranes. This is an indication of the transitional stage between tracheids and vessel elements. This study provides supportive evidence that lotus fibers are found in both helically thickened tracheids and helically thickened primitive vessels.     

Occurrence of plasmodesmata between differentiating vessels and other xylem cells inSorbus torminalis L. Crantz and their fate during xylem maturation

Summary The development of pit-pairs between differentiating xylem cells has been examined by transmission electron microscopy in young shoots ofSorbus torminalis. In some vessel-to-tracheid pits, as well as in previously studied intertracheid pits, a thickening of the pit membrane containing branched plasmodesmata was observed. A secondary wall-like cap was deposited over the thickening prior to cytoplasmic autolysis; some plasmodesmata, parallel to the plane of section, appeared to perforate the cap. At the end of the cell maturation stage, the central part of the primary wall thickening was hydrolysed, while the cap, including plasmodesmata remnants, appeared unaltered. In half-bordered pit-pairs between a parenchyma cell and a vessel or a tracheid, similar structures could be observed beside the conducting elements. When the vessel or tracheid matured, sealing of the pit membrane plasmodesmata resulted from the formation of a protective layer on the parenchyma-side rather than from the deposition of a cap on the conducting cell-side. These observations provide the first information on the presence of symplasmic connections in pits between differentiating vessels and neighbouring xylem cells. InS. torminalis, xylem differentiation is probably highly coordinated within a symplasmic domain; the persistence of such connections may account for the lack of specialization ofSorbus wood.     

Possible Mechanisms Limiting Movement of Ralstonia solanacearum in Resistant Tomato Tissues

The distribution and appearance of Ralstonia solanacearum in the upper hypocotyl tissues of root‐inoculated tomato seedlings of resistant rootstock cultivar LS‐89 (a selection from Hawaii 7998) and susceptible cultivar Ponderosa were compared to clarify the mechanism that limits the movement of the bacterial pathogen in resistant tomato tissues. In stems of wilted Ponderosa plants, bacteria colonized both the primary and the secondary xylem tissues. Bacteria were abundant in vessels, of which the pit membranes were often degenerated. All parenchyma cells adjacent to vessels with bacteria were necrotic and some of them were colonized with bacteria. In stems of LS‐89 plants showing no discernible wilting symptoms, bacteria were observed in the primary xylem tissues but not in the secondary xylem tissues. Necrosis of parenchyma cells adjacent to vessels with bacteria was observed occasionally. The pit membranes were often thicker with high electron density. The inner electron‐dense layer of cell wall of parenchyma cells and vessels was thicker and more conspicuous in xylem tissues of infected LS‐89 than in xylem of infected Ponderosa or mock‐inoculated plants. Electron‐dense materials accumulated in or around pit cavities in parenchyma cells next to vessels with bacteria, and in vessels with bacteria. Many bacterial cells appeared normal in vessels, except for those in contact with the pit membranes. These results indicate that R. solanacearum moves from vessel to vessel in infected tissues through degenerated pit membranes and that restricted movement in xylem tissues was the characteristic feature in LS‐89. The limitation in bacterial movement may be related to the thickening of the pit membranes and/or the accumulations of electron‐dense materials in vessels and parenchyma cells.     

PIT MEMBRANE REMNANTS IN PERFORATION PLATES OF PRIMITIVE DICOTYLEDONS AND THEIR SIGNIFICANCE

Perforations of vessel elements characteristically retain remnants of pit membranes (primary walls) in woods of species of more than 30 families of dicotyledons. Scanning electron microscopy is necessary to demonstrate presence and type of membrane remnant. Species with these remnants in perforations given in earlier literature as well as those newly reported here are listed. Perforation membrane remnants may take the form of flakes, strands, or webs, and particular types may characterize particular families (e.g., strands or bands in Illiciaceae). Some families have abundant perforation membrane remnants (e.g., Chloranthaceae, Illiciaceae). Where membranes are nearly intact, they are porose and closely resemble the porose pit membranes on end walls of Tetracentron tracheids. In Tetracentron, however, tracheary elements are monomorphic, so vessel origin cannot yet be said to have occurred. Membrane remnants in perforations are regarded as a relictual primitive feature that should be added to the list of primitive character states claimed for vessel elements in angiosperms; alternative hypotheses are considered and discussed, and evidence from DNA phylogenies is needed. In vessel-bearing dicotyledons with membrane remnants in perforations, many perforations are relatively clear, but an appreciable proportion of perforation plates do have membrane remnants.     

润楠属植物叶片和枝条水力特征的协同关系

以润楠属(Machilus) 7种植物成年个体为材料,对其进行生理指标测定,并对它们的叶片水分供需关系以及木质部纹孔特征和导水效率之间的关联进行分析。结果显示,润楠属7种植物相比原始被子植物具有更高的叶脉密度(VD),叶脉密度为9.8～14.1 mm/mm~2;气孔密度(SD)与叶脉密度呈显著正相关,说明叶片水分供需存在协同关系;气孔密度与气孔大小(GLC)呈负相关;气孔越大的叶片其膨压丧失点(TLP)的绝对值越低。枝条边材比导率(Ks)较低,为0.13～1.87 kg·m~(-1)·s~(-1)·MPa~(-1),且种间差异较大。叶脉和气孔密度均与边材比导率呈正相关。边材比导率与纹孔膜面积、纹孔口面积以及纹孔口长短轴比例相关性不显著。研究结果表明润楠属植物虽然叶脉密度较高,且木质部水分供应和叶片结构具有协同关系,但木质部解剖结构较为原始,导管多具梯形穿孔板,导水效率低,只能适应比较湿润的生境。     

Zinc Toxicity and Xylem Vessel Wall Alterations in White Beans

When white beans are exposed to excess zinc, reddish brown patchesappear along the leaf veins. Ultrastructural observations ofthe xylem vessels in the discoloured zones show several modificationsof the vessel walls including gelation of the pit membranes,coating of the lumen surface with an abnormal layer and depositionof electron-dense material in the secondary vessel walls. Histochemicalstudies indicate that the altered pit membranes and the coatinglayer stain positively for lipid, while the secondary wall depositsstain positively for phenolic compounds. Phaseolus vulgaris L., white bean, xylem vessels, zinc toxicity     

SEM studies on vessels in ferns. 11. Ophioglossum

With scanning electron microscopy (SEM), the nature of metaxylem vessel elements and tracheids was examined in Ophioglossum crotalophomides, 0. pendulum subsp. falcatum , and 0. vulgatum roots and rhizomes. Vessels were identified in all species. End walls of vessel elements, which bear perforations, are like lateral wall pitting of those elements in the secondary wall framework and differ only in absence of pit membranes or presence of pit membrane remnants. Some of the perforations contain pit membrane remnants that have large pores, small porosities, or are threadlike or weblike in structure. Dimorphic perforations were found in some vessel elements of rhizomes of 0. pendulum subsp. falcatum. Tracheids are very likely present in addition to vessels in all three species. The secondary wall framework of both tracheids and vessels is basically scalariform, although deviations in pattern are present. Vessel elements of Ophiglossum are entirely comparable to those of leptosporangiate ferns.