紫胶虫四种寄主树次生韧皮部与周皮的解剖学观察

紫胶虫的4种寄主树钝叶黄檀、南岭黄檀、木豆和苏门答腊金合欢的次生韧皮部轴向系统均由筛管、伴胞、韧皮薄壁细胞、纤维组成,径向系统由射线组成。木豆、苏门答腊金合欢中尚有少量石细胞。苏门答腊金合欢筛管分子端壁较倾斜,具复筛板,无明显的 P-蛋白质。其余3种筛管分子端壁均为横向,具单筛板,具 P-蛋白质。根据观察结果分析,4种寄主树2—3年生枝条或具表皮,或木栓层很薄;次生韧皮部的筛管看来均具相对较长的寿命;4种寄主中有3种筛管与伴胞均属特化程度高的类型。     

女贞和白蜡树的树皮结构及次生韧皮部发育的季节变化

女贞（ＬｉｇｕｓｔｒｕｍｂｕｃｉｄｕｍＡｉｔ）和白蜡树（ＦｒａｘｉｎｕｓｃｈｉｎｅｎｓｉｓＲｏｘｂ）是白蜡虫的两种主要寄主树。树皮由外向内为周皮,皮层,初生韧皮部的纤维束和次生韧皮部．它们的筛管分子具复筛板或单筛板,具Ｐ－蛋白质和筛管淀粉。伴胞为与筛管分等长的一列或单个细胞。筛管寿命在女贞中最长为一年,在白蜡树中则不超过８个月．形成层活动时间在女贞中是３月中下旬到１１月中旬,在白蜡树中是３月中下旬到１１月下旬．两种树木的木质部和韧皮部在３月中旬已开始分化,木质部和韧皮部分化停止的时间在女贞中分别是１１月中旬和１２月下旬;在白蜡树中分别是９月下旬和１１月下旬．两种树木在冬季都有部分分化的筛管分子,白蜡树中的部分分化的筛管分子于秋季形成,翌年３月中旬成熟,同年９—１０月瓦解。女贞枝条冬季平均保留１７０．２μｍ的具功能韧皮部区;而白蜡树在径向仅保留数列细胞宽的具功能韧皮都区越冬．     

美登木根的显微结构及其内生真菌的分布

本文采用石蜡永久制片和光学显微摄像的方法对美登木（Maytenus confertiflorus）根的显微结构及其内生真菌的分布进行了研究.结果表明,美登木根的次生结构由周皮和维管组织构成;周皮由木栓层、木栓形成层和栓内层组成,其中木栓层由5～6列长形细胞组成;维管组织中次生韧皮部所占根径的比例达46%,其薄壁细胞中内含物较丰富,次生木质部中分布有导管和木射线及少量木薄壁组织;在美登木木栓层和次生韧皮部中分布有菌丝片段、膨大的菌丝、菌丝团及分生孢子;内生真菌只在一定区域的皮层和次生韧皮部细胞中分布.     

凹叶厚朴细弱枝与粗壮枝导管分子的比较研究

对凹叶厚朴粗壮枝和细弱枝的次生木质部进行离析研究,发现其导管穿孔板有两种类型,即单穿孔板和梯状穿孔板。在细弱枝中,具不同类型穿孔板的导管分子有八种类型,即一端为单穿孔板的导管分子,另一端为梯状穿孔板的导管分子;只有一端为单穿孔板的导管分子;只有一端为梯状穿孔板的导管分子;两端均为单穿孔板的导管分子;两端均为梯状穿孔板的导管分子;具三个单穿孔板的导管分子;两端具单穿孔板的导管分子,中间具多个梯状穿孔板的导管分子;具多个梯状穿孔板的导管分子。粗壮枝除了无具多个梯状穿孔板的导管分子外,其它细弱枝的导管分子的类型都具有。细弱枝的导管分子宽而长,粗壮枝导管分子窄而短。     

美登木根的显微结构及其内生真菌的分布

本文采用石蜡永久制片和光学显微摄像的方法对美登木(Maytenus confertiflorus)根的显微结构及其内生真菌的分布进行了研究。结果表明, 美登木根的次生结构由周皮和维管组织构成; 周皮由木栓层、木栓形成层和栓内层组成, 其中木栓层由5～6 列长形细胞组成; 维管组织中次生韧皮部所占根径的比例达46%, 其薄壁细胞中内含物较丰富, 次生木质部中分布有导管和木射线及少量木薄壁组织; 在美登木木栓层和次生韧皮部中分布有菌丝片段、膨大的菌丝、菌丝团及分生孢子; 内生真菌只在一定区域的皮层和次生韧皮部细胞中分布。     

降香黄檀着叶期和无叶期次生韧皮部筛分子的超微结构

利用透射电镜技术研究了生长在海南岛的热带落叶树降香黄檀(Dalbegia odorifera T.Chen)1—2年生枝条着叶期和无叶期次生韧皮部筛分子的超微结构,并就这两个时期的筛分子进行了比较。着叶期每个成熟筛分子内有一个带尾的纺锤形P-蛋白质体,主体由稠密而散乱的P-蛋白质细纤维组成,尾部呈结晶状;筛分子具有横向端壁和单筛板,在邻近筛板处,细胞壁向筛分子腔内形成明显的突起。无叶期仍然保持着与着叶期大致相同厚度的有功能韧皮部,筛分子具有正常的原生质体,P-蛋白质和筛板孔的结构也与着叶期的相同,但筛分子内有较多的淀粉粒和囊泡。     

白鲜根的发育解剖学研究

应用半薄切片、常规石蜡切片并结合离析法,对药用植物白鲜(Dictamnus dasycarpus Turcz.)根的发生发育过程进行了研究。结果表明:白鲜根的发生发育过程包括4个阶段,即原分生组织阶段、初生分生组织阶段、初生结构阶段以及次生结构阶段。原分生组织位于根冠内侧及初生分生组织之间,衍生细胞分化为初生分生组织。初生分生组织由原表皮、基本分生组织以及中柱原组成。原表皮分化为表皮,基本分生组织分化为皮层,中柱原分化为维管柱,共同组成根的初生结构;在初生结构中,部分表皮细胞外壁向外延伸形成根毛,皮层中分布有油细胞,内皮层有凯氏带,初生木质部为二原型或偶见三原型,外始式;根初生结构有髓或无。次生结构来源于原形成层起源的维管形成层的活动以及中柱鞘起源的木栓形成层的活动;白鲜次生韧皮部宽广,其中多年生根中可占根横切面积的85%,另外除基本组成分子外,还分布有油细胞;周皮发达,木栓层厚;初生皮层、次生木质部和次生韧皮部薄壁细胞中常充满丰富的淀粉粒。     

杨柳科(Salicaceae)7种植物次生韧皮部的比较研究

本文研究和比较了杨柳科2属7种植物次生韧皮部解剖结构。结果表明:(1)杨属和柳属植物在次生初皮部解剖上有某些共同特征:次生韧皮部具有明显分层现象;韧皮纤维和含晶细胞与筛管分子、伴胞和韧皮薄壁组织细胞是切向带相间排列;筛管分子均为复筛板,端壁倾斜平均含有7-8个筛域。(2)两属植物在射线和晶体类型上有明显区别:柳属植物次生韧皮部无石细胞;杨属植物不具功能韧皮部中含有石细胞。(3)两属植物均有一些较为原始的韧皮部解剖特征。     

杨柳科7种植物次生韧皮部的比较研究

本文研究和比较了杨柳科２属７种植物次生韧皮部解剖结构。结果表明：１杨属和柳属植物在次生韧皮部解剖上有某些共同特征：次生韧皮部具有明显分层现象;韧皮纤维和含晶细胞与筛管分子,伴胞和韧皮薄壁组织细胞呈切向带相间排列;筛管分子均为复筛板,端壁倾斜平均含量有７－８个筛域。２两属植物在射线和晶体类型上有明显区别：柳属植物次生韧皮部无石细胞;杨属植物不具功能韧皮中含有石细胞。３两属植物均有一些较为原始的韧皮剖     

10种卫矛科植物次生韧皮部的比较解剖

研究了卫矛科（Ｃｅｌａｓｔｒａｃｅａｅ）５ 属１０ 种植物次生韧皮部的结构。根据筛管分子、韧皮射线及厚壁组织的结构特征,将这１０ 种植物次生韧皮部分为３ 种类型。类型Ⅰ：筛管分子端壁倾斜,筛域数多,都为复筛板,韧皮射线大多为单列。卫矛属（Ｅｕｏｎｙｍ ｕｓ）的５ 种植物属于这一类型;类型Ⅱ：包括南蛇藤属（Ｃｅｌａｓｔｒｕｓ）和雷公藤属（Ｔｒｉｐｔｅｒｙｇｉｕｍ ）,其特征是筛管分子短,端壁倾斜度小,筛域数少,纤维不木质化,射线多列;类型Ⅲ：筛管分子多为单筛板,端壁接近水平,在不具功能韧皮部出现成簇的石细胞和纤维,射线单列或两列。属于此类型的有十齿花属（Ｄｉｐｅｎｔｏｄｏｎ）和核子木属（Ｐｅｒｒｏｔｔｅｔｉａ）     

The Phloem of Nelumbo nucifera Gaertn

In common with other aquatic angiosperms, Nelumbo nucifera Gaertn.has a relatively strongly developed phloem tissue. The vascularsystem consists of discrete collateral bundles in which no cambiumdevelops and the phloem and xylem are separated by a narrowlayer of parenchyma cells. The phloem consists of sieve elements,companion cells, and phloem parenchyma cells. The sieve elementshave transverse end walls with simple sieve plates. The cellsattain considerable width in the late phloem (metaphloem). Thecompanion cells are in vertical strands. In the early phloem(protophloem) of large bundles the sieve tubes and companioncells are eventually obliterated. The parenchyma cells alsoform vertical strands which may contain tannin cells. Some parenchymacells and companion cells are binucleate. The sieve elementsshow ultrastructural features common for these cells in dicotyledons.At maturity, they lack nuclei, ribosomes, and tonoplasts, butretain a plasmalemma, mitochondria, and plastids. The latterare poorly differentiated and form starch. The endoplasmic reticulumis in part stacked, in part it forms a network next to the plasmalemma.The P-protein occurs in two forms. One consists of tubules notassembled in any specific type of array. The other, possiblycomposed of much extended tubules, is assembled in crystallineaggregates which are retained as such in mature cells. The sieveplate pores are lined with callose and plasmalemma. The lateralwalls are relatively thin and the nacreous layer varies in degreeof distinctness.     

Feeding Position of Laccifer lucca on Dalbergia balansae and the Influence of Parasitism on Bark Structure

When Laccifer lacca fed in the bark of Dalbergia balansae, the penetration in the bark by a stylet was mainly intracellular, seldom intercellular. Finally, the stylet arrived at the funtional sieve element, and fed in it. The tip of tt,e stylet was at a distance of 0.48–0.78 mm from the surface of periderm. 70.3% of the stylets fed in the zone of newly-differentiated sieve elements. The fed sieve element had P-protein and callose, and exhibited no serious reaction of injury. The parenchyma cells that were pierced through by the stylet and the neighbouring cells Lad obvious reaction of injury, such as: thickened cytoplasm and plasmolysed; dark stained nuclei; smaller starch grains and intracellular deposition of concentrated golden material. The stylet that pierced through the bark was encircled by a stylet sheath consisted of proteins. The stylet sheath looked like a string of beads as a whole. Branching stylet sheath was observed. Some branches even reached far into the xylem, but the stylet finally reached the sieve element. At the same time, the stylet might penetrate through many sieve elements, finally reach newly-differentiated sieve elements. These results suggest that feeding of Laccifer lacca was a process of initiative choice. Two years after collecting shellac by means of skinning instead of cutting the branch, tb.e stylets and styler sheaths still remained in the bark. Several layers of ceils around them were dead and fully imbued with yellow-brown material. Stylers and styler sheaths in the outer cortex were surrounded by bending phellogen and separated from the living cells, forming many cyst-like structures in the periderm. Such bark should not be further used for feeding.     

Seasonal Variations of Secondary Phloem Development in Pterocarya Stenoptera and Its Relation to Feeding of Kerria yunnanensis

Early in April of 1987, cells in an undifferentiated state which overwintered on the phloem side of the cambial zone in the branch of Pterocarya stenoptera began to differentiate into merebets of phloem. Cambium divided actively in mid-April and ceased to decide by early-Novembet. Five to eleven bands of fibers alternating with the bands of sieve tubes, companion cells and phloem parenchyma cells produced every year. By mid to late April, new xylem differentiation began. Phloem and xylem differentiation ceased almost simultaneously. Functional sieve tube elements were present all the year round in the phloem. During winter, most sieve tubes produced in the current year ceased functioning, leaving only the zone of functional sieve tube of several rows of cells in width with open pores in the sieve plates. These sieve tubes did not collapse until mid-May. In October, several rows of partially differentiated sieve elements appeared near the cambial zone. They still possessed nuclei. The companion cells had produced but no P-protein. They matured during April of the following year and collapsed by July to September. The life span of sieve elements extended for 8 months at the most. In winter, there were less functional sieve tubes in the branch. This may be one of the reasons that only few Kerria yunnanensis survive on the branch of Pterocarya stenoptera.     

当归根显微结构及其根腐病真菌分布研究

利用徒手切片、石蜡切片和超薄切片及显微摄像的方法,对当归根的显微结构及根腐病致病真菌的分布进行了研究。结果表明:当归的根由周皮和次生维管组织两部分组成,周皮由外向内依次分为木栓层、木栓形成层、栓内层;次生韧皮部占根径的比例在60%以上,主要成分包括筛胞、韧皮薄壁细胞、韧皮纤维和分泌道,薄壁细胞富含淀粉粒等营养物质;次生木质部由导管、木薄壁细胞和木射线组成,木质部呈多元形,木射线和韧皮射线明显。在根的周皮细胞和中柱中均有真菌分布,说明真菌由木栓层、木栓形成层、栓内层依次向里侵入到韧皮薄壁细胞,在薄壁细胞内定殖并形成菌丝结或团块状结构,进而扩展成一定的侵染区域;真菌不仅侵染周皮和韧皮部,而且还进一步侵染木质部并破坏导管。此外,研究还发现,淀粉粒是真菌定殖的主要场所,真菌穿透或缠绕在淀粉粒上,并利用其营养不断地生长与繁殖。     

The distribution of P-Protein in mature sieve elements of celery

Summary The extent of blocking of sieve-plate pores caused by release of cell turgor was investigated by fixing and processing for electron microscopy a long length of celery (Apium graveolens L.) phloem. Differences in distribution of P-protein within the pores were observed between those cells near the two cut ends, and the central cells.To assess the effect of chemical fixation on the distribution of P-protein, strands of celery phloem (fixed or unfixed, and not treated with cryoprotectants) were frozen in Freon 12 and then freeze-substituted. In sieve elements from unfixed tissue there were a greater number of sieve plates displaying partially open pores.Direct freezing of unprotected phloem tissue in Freon 12 resulted in the formation of ice crystals within the lumen of the sieve elements. Freezing of tissue at rates fast enough to avoid the formation of damaging ice crystals resulted in sieve-plate pores having an unoccluded central channel with a peripheral lining of P-protein. In the lumen of the sieve elements the P-protein filaments occurred as discrete bundles ca. 0.5 m in diameter, and as a parietal layer varying in thickness from 0.1 to 0.5 m.     

Distribution of leaf assimilates in the stem of Picea abies L.

Summary Autoradiographic and microautoradiographic studies of 2-year-old Picea abies plants show that in summer leaf assimilates from the second-year shoot are translocated basipetally. Leaf assimilates are first transported to the stem via leaf trace phloem, then to the base of the stem in the sieve cells of the latest increment of secondary phloem. On the way down leaf assimilates move radially from sieve cells into cells of the phloem parenchyma, the vascular cambium, the rays, the inner periderm and certain cells of pith and cortex, including the epithelial cells surrounding the resin ducts. Other cells of pith and cortex remain nearly free of label, despite the long translocation time (20 h). With the exception of the vascular cambial cells, the stem cells that gain leaf assimilates by radial distribution coincide with those that contain chlorophyll and starch.     

Wound phloem in transition to bundle phloem in primary roots ofPisum sativum L.

Summary 48 hours after interrupting the root stele ofPisum, wound phloem initiated (proximally or distally to the wound) to reconnect the vascular stumps was found to contain some nucleate wound-sieve elements. At the elongating end of an incomplete wound-sieve tube these elements exhibit a sequence of ultrastructural changes as known from protophloem-sieve tubes. Elongation occurs by the addition of newly divided (wound-) sieve-element/companion-cell complexes. In order to dedifferentiate and assume a new specialization formerly quiescent stelar or cortical cells require at least one (mostly more) preliminary division. Companion cells are consequently obligatory sister cells to wound-sieve elements.By reconstruction using serial sections it could be shown that wound-sieve tubes elongate bidirectionally, starting in an early activated procambial cell of the stele. The elongation is directed by the existence of plasmodesmata, preferably when lying in primary pit fields, and by the plane of preceding divisions. Thus, the developing wound-sieve tube can deviate from the damaged bundle and radiate into the cortex as soon as the plane of the preceding divisions is favourable. In the opposite direction, elongating wound-sieve tubes run parallel to pre-existing phloem traces, thus broading their base at the bundle for the deviating part of the wound-sieve tube. Frequently an individual wound-sieve tube is supplemented at the bundle by a further wound-sieve tube which is partly running parallel to it. Both sieve tubes are interlinked with sieve plates by three-poled sieve elements.Ultrastructurally, the developmental changes of nucleate wound-sieve elements follow the known pattern. In spite of its contrasting origin and odd shape a mature wound-sieve element eventually has the same contents as regular sieve elements: sieve-element plastids, mitochondria, stacked ER and small amounts of P-protein within an electronlucent cytoplasm.     

Ultrastructure of minor veins inCucurbita pepo leaves

Summary The minor veins ofCucurbita pepo leaves were examined as part of a continuing study of leaf development and phloem transport in this species. The minor veins are bicollateral along their entire length. Mature sieve elements are enucleate and lack ribosomes. There is no tonoplast. The sieve elements, which are joined to each other by sieve plates, contain mitochondria, plastids and endoplasmic reticulum as well as fibrillar and tubular (190–195 diameter) P-protein. Fibrillar P-protein is dispersed in mature abaxial sieve elements but remains aggregated as discrete bodies in mature adaxial sieve elements. In both abaxial and adaxial mature sieve elements tubular P-protein remains undispersed. Sieve pores in abaxial sieve elements are narrow, lined with callose and are filled with P-protein. In adaxial sieve elements they are wide, contain little callose and are unobstructed. The intermediary cells (companion cells) of the abaxial phloem are large and dwarf the diminutive sieve elements. Intermediary cells are densely filled with ribosomes and contain numerous small vacuoles and many mitochondria which lie close to the plasmalemma. An unusually large number of plasmodesmata traverse the common wall between intermediary cells and bundle sheath cells suggesting that the pathway for the transport of photosynthate from the mesophyll to the sieve elements is at least partially symplastic. Adaxial companion cells are of approximately the same diameter as the adaxial sieve elements. They are densely packed with ribosomes and have a large central vacuole. They are not conspicuously connected by plasmodesmata to the bundle sheath.     

Fine structure,pattern of division,and course of wound phloem in Coleus blumei

The wound phloem bridges which have developed six days after interrupting an internodal vascular bundle contain wound sieve-elements, companion cells, and phloem parenchyma cells. An analysis of the meristematic activity responding to the wounding clearly demonstrates that three consecutive divisions are prerequisite to the formation of phloem mother-cells. Companion cells are obligatory sister cells of wound sieve-elements, connected to the latter by specific plasmatic strands and provided with a dense protoplast. Six days after wounding most of the wound sieve-elements are still at a nucleate state of development, but already have characteristic P-protein bodies and plastids containing sieve-element starch. Their cytoplasmic differentiation corresponds to the changes recorded during maturation of ordinary sieve elements. Sieve-plate pores penetrate through preexisting parenchyma cell walls, only, and develop from primary pitfield-plasmodesmata. Wound sieve-elements do not connect to preexisting bundle sieve-elements, they open a new tier of young sieve elements produced by cambial activity.