The anatomy of roots and mycorrhizae of the orchidDendrobium cunninghamii Lindl

The root cap develops out of the cells of the caliptrodermatogen. The root apex belongs to the first of Haberlandt’s histogen types. The velamen usually consists of three layers of cells, and develops out of the protoderm by periclinal divisions. Funnel-shaped cells later divide tangentially into two cells, and in one of these cells a fibrous body develops. Two to four thick-walled cells alternate, usually with one passage cell in the exodermis. The cortex proper consists of approximately ten to twelve layers of parenchymatic cells in the mature root. There are eight to sixteen xylem poles alternating with the same number of phloem poles in the central cylinder. In the roots ofDendrobium cunninghamii I observed two types of mycorrhizal infection, which can be classified as transitive types between ptyophagus and tolypophagus mycorrhizae. In my opinion, a state of balanced symbiosis exists between the fungus and the plant; a part of the time the plant acts as a parasite on the fungus.     

喀斯特地区莎叶兰的解剖构造及其环境适应性

以广西西北部雅长兰科植物保护区的莎叶兰( Cymbidium cyperifolium)为对象,采用石蜡切片法对莎叶兰叶片和根的解剖构造及其对喀斯特环境的适应性进行了研究。结果表明：(1)莎叶兰叶片的上表皮覆盖有较厚的角质层,气孔均分布于下表皮,且凸出表皮细胞之上;各表皮性状在叶片不同部位存在显著差异,叶片下部的气孔密度、气孔指数和气孔长度最大,表皮细胞密度以叶片上部的最大;叶片属于等面叶,叶肉无栅栏组织和海绵组织的分化;叶脉为明显的平行脉,且粗细交互分布;(2)莎叶兰根的横切面包括根被、皮层、中柱3部分,其中根被细胞排列紧密,为生活细胞;皮层由薄壁细胞组成;根部维管束属于辐射维管束,14原型。菌根粗壮,稀根毛,共生真菌主要分布于根被及皮层中,菌丝体通过根被薄壁细胞间隙及内、外皮层的通道细胞进行侵染。(3)莎叶兰叶片和根的结构不仅有湿生植物特征,如叶片相对较薄、气孔少且凸出表皮细胞、冠/根比值大等;还有旱生植物的特征,如叶片角质层较厚、机械组织发达、细胞结构紧密、具含晶细胞,肉质根具根被,内、外皮层细胞壁明显增厚等。这些结构是莎叶兰对当地缺水、干湿季明显、分布于林下多石砾土壤的生长环境的一种高度适应性表现。     

密花石斛等六种兰科植物菌根的显微结构研究

本文对密花石斛等六种兰科植物根的显微结构进行了比较观察。结果表明,它们具有典型的兰科植物根,具根被和发达的皮层组织,皮层细胞内分布有针状结晶和菌根真菌形成的菌丝结,发现菌根真菌通过外皮层薄壁通道细胞或破坏根被组织和外皮层细胞侵入皮层细胞,形成内生菌根。     

密花石斛等六种兰科植物菌根的显微结构研究

本文对密花石斛等六种兰科植物根的显微结构进行了比较观察。结果表明,它们具有典型的兰科植物根,具根被和发达的皮层组织,皮层细胞内分布有针状结晶和菌根真菌形成的菌丝结,发现菌根真菌通过外皮层薄壁通道细胞或破坏根被组织和外皮层细胞侵入皮层细胞,形态内生菌根。     

TILOSOMES IN ROOTS OF ORCHIDACEAE: MORPHOLOGY AND SYSTEMATIC OCCURRENCE

Tilosomes, also called “fibrous bodies” or “rod bodies” in older literature, are lignified excrescences from the walls of cells of the innermost velamen cell layer adjacent to thin-walled passage cells of the exodermis in roots of many epiphytic orchids. Seven broad morphological types are recognized: spongy, lamellate, discoid, webbed, meshed, baculate, and plaited. Some types characterize specific genera or subtribes of Orchidaceae. Of the 350 species in 175 genera included in a survey of the family, tilosomes occur in 95 species and 39 genera and are concentrated in tribe Polystachyeae and subtribes Sobraliinae, Coelogyninae, Laeliinae, Pleurothallidinae, Bulbophyllinae, Lycastinae, and Maxillariinae. With the exception of the pantropical genera Bulbophyllum and Polystachya and the Paleotropical subtribe Coelogyninae, tilosomes are almost exclusively Neotropical phenomena.     

Impatiens macrantha (Balsaminaceae) sp. nov., a new species from limestone areas in Guangxi,China

Impatiens macrantha S. X. Yu&Ying Qin (Balsaminaceae), a new species from Guangxi, China, is described and illustrated. Phylogenetic analysis based on molecular data shows the new species to belong to I. subg. Clavicarpa and to be closely related to I. tubulosa with which it shares succulent stems and racemose inflorescences, but it can be easily distinguished by having a 4 – or 5 – ridged stem, obovate or elliptic leaf blade, and saccate lower sepal. Furthermore, I. macrantha is distinguishable from other Impatiens in China by its obviously larger leaves and flowers. The evidence from morphology and molecular data both support I. macrantha as new to science.     

PHYLOGENETIC COMPARISON OF LARGE NUCLEAR DNA CONTENTS OF DIFFERENTIATED CELLS IN THE ROOTS OF EQUISETUM,TRADESCANTIA, AND HORDEUM

Nuclear DNA of meristematic, epidermal and root cap cells from the roots of three vascular plants—the cryptogam, Equisetum hyemale L, and the phanerogams, Tradescantia Clone 02 and Hordeum vulgare L.—was measured with quantitative Feulgen microspectrophotometry. Epidermal cells of all three species and root cap cells in both phanerogams contained up to 8fold the amount of nuclear DNA found in their respective meristematic telophase nuclei. In general, the large amounts of nuclear DNA parallel development and differentiation in the epidermis regardless of phylogeny, habitat, or degree of domestication. However, comparisons of the increase in nuclear DNA contents in the various epidermal cell types among these three species suggest that the mechanisms giving rise to these increases may differ phylogenetically and may represent another character in which cryptogams and phanerogams diverged in their evolution.     

Die Ionenaufnahme durch die Luftwurzel vonEpidendrum

Summary The uptake of³⁵SO₄ ^–– by aerial roots ofEpidendrum was investigated using microautoradiographic techniques. During a 30 min application to the velamen the isotope is transported through the cortex and the passage cells of the endodermis and pericycle and accumulated into the protoxylem vessels. The results are discussed with regard to the general problem of ion uptake into the xylem.     

ULTRASTRUCTURE OF THE FLAGELLA OF THE COLORLESS PHAGOTROPH PERANEMA TRICHOPHORUM (EUGLENOPHYCEAE).II. FLAGELLAR ROOTS1

Peranema trichophorum (Ehrenberg) Stein, a colorless phagotrophic euglenoid flagellate, has a typically euglenoid microtubular root complement. Striated root components, relatively uncommon in euglenoids, are connected to the basal bodies and to a microtubular root. The flagellar system of Peranema consists of three unequal microtubular roots which extend anteriorly beneath the reservoir membrane, and narrow-band striated roots (periodicity = 29–33 nm) which connect one of the four basal bodies to the movable rodorgan of the feeding apparatus. An inter basal body striated fiber forms a three-way connection between one particular microtubular root, a flagellar basal body, and the striated roots. A striated fibril (periodicity = 18–25 nm), which may be an extension of the striated root system, extends beneath the reservoir membrane. Associated with the striated fibril and the striated roots are cisternae of smooth endoplasmic reticulum.     

The root-tuber anatomy of Asphodelus aestivus

The root tubers of Asphodelus aestivus consist mostly of enlarged fleshy storage tissue. They are bounded by a multiple-layered velamen, responsible for rapid water uptake, water loss reduction, osmotic and mechanical protection. In the cortex area, thin-walled idioblasts contain numerous raphides of calcium oxalate in their large vacuole with a distinctive tonoplast. Wide morphological variations are observed among the raphide cross sections. Electron-dense compounds penetrate the raphide surface and raphide groove. Raphides seem to be vital for the protection of the root tuber parenchyma from herbivores. The cells of uniseriate endodermis are heavily thickened possessing a few plasmodesmata. The vascular cylinder is 20–28-arch and the root xylem consists of vessels in short radial rows, alternating with clusters of phloem cells. The presence of cells, which contain soluble polysaccharides in their large vacuole, is conspicuous after employing the Schiff's reagent. Exodermis cells and all cell walls, especially the thick ones of the endodermis, are also stained. Numerous parenchyma cells, especially those around vascular bundles are stained intensely, when exposed to Sudan Black B. These cells occurring as solitary idioblasts abundantly accumulate oil. Electron-dense remnants are evident within the vacuoles of the storage cells especially near the vascular tissue. The morphological features of A. aestivus root tubers and the major part of the total plant biomass are responsible for the species’ occurrence and frequent dominance in a wide array of arid environments. A. aestivus possessing root tubers is proved to be very efficient in storing water during the long summer drought, less susceptible to climatic stress and well synchronized with the climatic fluctuations of the Mediterranean environment.     

Subterranean axes in tribe Diurideae (Orchidaceae): Morphology,anatomy, and SYSTEMATIC SIGNIFICANCE

The morphological and anatomical nature of perennating storage organs of the predominantly Australasian orchid tribe Diurideae (Orchidoideae: Orchidaceae) as well as anatomical concepts in tribes Orchideae and Diseae of Orchidoideae have been problematic for 150 yr, reflected in conflicting or vague terminology and questions about polystely and even monophyly of Orchidoideae. From a representative survey of underground organs of 145 species in 37 ingroup genera (Diurideae) and two outgroup genera (Spiranthes and Disa), the so-called “root-stem tuberoids” are here interpreted as root tubers (except for the stem tubers of Rhizanthella) borne on either droppers or stolonoid roots. All root tubers examined are bounded by a 1–4 layered velamen and exodermis, whereas droppers and stolonoid roots may have velamen-exodermis or a simple epidermis depending on the taxon and often bear multiseriate or uniseriate trichomes associated with mycorrhiza (as do roots of some taxa). The “polystely” reported in tubers of many Orchideae also occurs in tubers of many Diurideae but represents only dissection of the siphonostele into 2–13 traces. Cladistic analyses of data show extraordinarily high levels of homoplasy in characters related to root, dropper/stolonoid root, and tuber, so that these characters alone are of limited usefulness.     

Root tubercles in apostasiad orchids

Tubercles are swollen, stalked, warty branches arising from the main elongated roots of species in the terrestrial orchid genus Apostasia (subfamily Apostasioideae). Generalized anatomy resembles that of the main roots, except tubercles lack a velamen and conductive strands are few. There are multinucleate cortical cells, and stomata occur in the epidermis. Pores of stomata appear to be permanently open and thus may enhance the interchange of gases between root tissues and soil under the moist conditions in which apostasias grow. Multicellular warts seem to function as holdfasts and are points of entry for mycorrhizal fungi.     

大花地不容块根生物碱成分的研究

为研究大花地不容块根的生物碱成分,该研究采用酸提碱沉法从大花地不容块根中提取出总生物碱,通过硅胶柱色谱法和制备液相色谱技术对大花地不容块根的总生物碱提取物进行分离纯化,并利用波谱学手段对化合物进行结构鉴定。结果表明:(1)从总生物碱提取物中分离得到11个化合物,分别鉴定为青藤碱(1)、青风藤碱(2)、斯帝酚灵碱(3)、瑞枯灵(4)、异紫堇定(5)、紫堇单酚碱(6)、巴婆碱(7)、sukhodianine(8)、荷包牡丹碱(9)、7-氧代克班宁(10)和巴马汀(11)。(2)体外细胞毒性测试显示,大花地不容总生物碱和其主成分青藤碱对人类肺癌细胞A549的IC₅₀值分别为7.5×10^-4 g·mL^-1和6.59×10^-9 g·mL^-1。化合物2、3、4、7、8、9和10系首次从大花地不容中分离得到。大花地不容块根中含有吗啡烷、原阿朴啡、阿朴啡、苄基四氢异喹啉和原小檗碱5种类型的生物碱。     

THE DEVELOPMENT OF THE SEED OF ABUTILON THEOPHRASTI I. OVULE AND EMBRYO

Winter , Dorothy M. (Iowa State U., Ames.) The development of the seed of Abutilon theophrasti. I. Ovule and embryo. Amer. Jour. Bot. 47(1): 8–14. Illus. 1960.—Abutilon theophrasti Medic, is a widespread annual weed which produces an abundance of seed in capsules which mature within 20 days after pollination. Ovule differentiation may be observed at least 8 days before anthesis when a sporogenous cell becomes evident and 2 integuments are initiated. An 8-nucleate embryo sac is produced from the chalazal megaspore approximately 2 days before anthesis. The outer integument of the mature campylotropous ovule consists of 2 cell layers, the inner integument has 6 to 15 cell layers. The initially free-nucleate endosperm becomes cellular betwen 3 and 7 days after pollination. At maturity a thin layer of gelatinous endosperm encases the embryo. The Asterad-type proembryo of Abutilon has a stout suspensor and develops rapidly. Four days after pollination cotyledons are initiated; 4 days later a leaf primordium is evident. Fifteen days after pollination the embryo, which has essentially completed its growth, consists of a large hypocotyl with root promeristem and root cap at its basal end, and 2 flat, folded, leaflike cotyledons enclosing a small epicotyl at its upper end. The epicotyl consists of an embryonic leaf and a stem apex.     

Digestive Retention Times in Forest Guenons (Cercopithecus spp.) with Reference to Chimpanzees (Pan troglodytes)

Because the length of time food is maintained in the gut influences fermentation rates and its overall digestibility, information on digestive passage rates is critical to explain the overall feeding and foraging strategy of a species. I present results from digestive passage experiments conducted on captive Cercopithecus ascanius, C. mitis, C. neglectus, Miopithecus talapoin, and Pan troglodytes. I recorded several measures of digestive passage time, including transit time (time of first marker appearance; TT), mean retention time of markers (MRT), and time of last appearance of a marker (TLA). I conducted 4 trials on each of the 10 subjects. A trial consists of the administration of 20, non-toxic colored plastic markers. Overall, the 5 species varied in digestive times (p < 0.01), but there is no difference between Cercopithecus neglectus and Pan troglodytes (p = 0.131) or between C. mitis and C. ascanius (p = 0.661). When the effect of body size is removed (by computing the ratio y/x, where x = body mass, and y = MRT), Pan troglodytes exhibits a low ratio, suggesting relatively slow retention times in the 4 cercopithecines. My findings and other published digestive passage rates suggest that lengthy digestive retention times may be characteristic of cercopithecines. These data may help to interpret how the smaller-bodied guenons are able to consume a higher percentage of fiber than that of chimpanzees, a specialized frugivore. Small body size, in combination with long digestive passage times may be an adaptation on the part of Cercopithecus species to consume a high fiber diet, while maintaining a greater capacity to detoxify secondary metabolites.     

THE FLAGELLAR APPARATUS OF CHRYSOLEPIDOMONAS DENDROLEPIDOTA (CHRYSOPHYCEAE), A SINGLE-CELLED MONAD COVED WITH ORGANIC SCALES1

The flagellar apparatus of Chrysolepidomonas dedrolepidota Peters et Andersen is similar to that of other members of the Ochromonadales, Chrysophyceae. there are four microtubular roots (R_1-4) and a system II fiber (= rhizoplast). the R₁ root consists of three microtubules that nucleate many cytoplasmic microtubules. One compressed band of 10 or more cytoplasmic microtubules is directed black along the R1 root in an anti-parallel direction. The R₂ root consists of one to two microtubules, and it extends toward the distal end of the R₁ root. The R₃ root consists of six (?seven) microtubules near its proximal end. The “a” and “f” microtubules of the R₃ root are under the short flagellum, and the “f” microtubule loops back and under the basal body, extending down to the nucleus. The R₄ root consists of one to two microtubules extending along the left side of the shot flagellum and curving under the short flagellum where it terminates near the “a” microtubule of R₃ Both flagella have a transitional plate and a transitional helix with five gyres. There is a thin, second plate in the basal body at the level of the distal end of the “c” tubules of the basal body triplets. The tripartite flagellar hairs have long lateral filaments but lack short lateral filaments. We compare the flagellar apparatus with that of other members of the Ochromonadales and members of the Hydrurales and Hibberdiales.     

SHOOTLESSNESS,VELAMENTOUS ROOTS,AND THE PRE-EMINENCE OF ORCHIDACEAE IN THE EPIPHYTIC BIOTOPE

Roots of representative epiphytic orchids were examined for anatomical detail, desiccation resistance and evidence of CAM activity. Those “shootless” taxa examined (Campylocentrum pachyrrhizum (Reichenb. f.) Rolfe, Harrisella porrecta Reichenb. f.) Fawc. & Rendle, and Polyradicion lindenii (Lindl.) Cogn. ex Urban) and a semi-shootless type (Kingidium taeniale (Lindl.) P. F. Hunt) bear thinner or eroded velamina and greater volumes of cortical intercellular space than do those of the leafy forms tested (Campylocentrum sellowii (Reichenb. f.) Rolfe, Encyclia tampensis (Lindl.) Small, Epidendrum radicans Pavon ex Lindl., Phalaenopsis amabilis (L.) Blume, Rangaeris amaniensis (Krzl.) Summerhayes and Vanda parishii (Reichenb. f.)). Shootless species also bear a more elaborate aeration apparatus at the velamen-cortex interface. Structurally distinct cortical cells located in this region may regulate gas exchange across the exodermis. Velamen thickness varies greatly among the ten species, as does the development of outer tangential walls of U cells in the underlying exodermis. Desiccation resistance under laboratory conditions was more closely related to root surface-to-volume ratio (S/V) than to any other measured anatomical parameter, including velamen development. Modes of carbon gain and the possible pathway for movement of fungus-borne carbon into an orchid's pool of assimilates are described, as is the possible significance of these processes to survival in forest canopy habitats.     

SHOOT APEX ORGANIZATION AND ORIGIN OF THE RHIZOME-BORNE ROOTS AND THEIR ASSOCIATED GAPS IN DENNSTAEDTIA CICUTARIA

The shoot apex of Dennstaedtia cicutaria consists of three zones—a zone of surface initials, a zone of subsurface initials, and a cup-shaped zone that is subdivided into a peripheral region and central region. A diffuse primary thickening meristem, which is continuous with the peripheral region of the cup-shaped zone, gives rise to a broad cortex. The roots occurring on the rhizomes are initiated very near the shoot apex in the outer derivatives of the primary thickening meristem. The roots that occur on the leaf bases also differentiate from cortical cells. Eventually, those cortical cells situated between the newly formed root apical cell and the rhizome procambium (or leaf trace) differentiate into the procambium of the root trace, thus establishing procambial continuity with that of the rhizome or leaf trace. Parenchymatous root gaps are formed in the rhizome stele and leaf traces when a few of their procambial cells located directly above the juncture of the root trace procambium differentiate into parenchyma. As the rhizome procambium or leaf trace continues to elongate, the parenchyma cells of the gap randomly divide and enlarge, thus extending the gap.     

Vegetative anatomy of subtribe Orchidinae (Orchidaceae)

Leaves in Orchidinae are essentially glabrous; anticlinal walls of foliar epidermal cells arc basically straight-sided to curvilinear, and cells arc fundamentally polygonal on both surfaces; adaxial cells are larger than abaxial cells. Stomata arc anomocytic and usually only abaxial and superficial; substomatal chambers are small to moderate; outer and inner guard cell ledges are mostly small. There is no hypodermis nor are there fibre bundles. Mesophyll is homogeneous, chlorcnchyma cells arc thin-walled, and intercellular spaces numerous. Crystalliferous idioblasts abound. Vascular bundles are collateral, organized in a single series. and lack associated sclerenchyma. Bundle sheath cells are thin-walled and chlorophyllous. Stems are glabrous; stomata arc frequent in one species, lacking in others. Cortical cells are oval to circular, thick-walled, and interspersed with triangular intercellular spaces. Ground-tissue cells are circular, and triangular intercellular spaces are present. Vascular bundles arc collateral and scattered throughout the ground-tissue or are absent from the central ground-tissue. Epidermis in absorbing roots is one-layered and non-velamcntous. Exodcrmal cells are thin-walled and dead cell walls bear tenuous scalariform bars; some species lack an exodermis. Outer cortical cells are polygonal and lack intercellular spaces; middle layer cortical cells are rounded with triangular intercellular spaces; inner layer cells are polygonal and lack intercellular spaces. Endodermis and pericycle are thin-walled and one-layered. Vascular cylinder is mostly 7–9-arch with xylcm and phloem components alternating regularly; vascular tissue is embedded in parenchyma; pith cells are parenchymatous, polygonal, thin-walled and lack intercellular spaces. Root tubers generally bear a velamen of variable thickness; bulbous-based unicellular hairs frequently form a dense mat; exodermal cells are thin-walled; dead cells have scalariform bars, passage cells are sparse. Ground-tissue consists of rounded water-storage and assimilatory cells interspersed with triangular or quadrangular intercellular spaces; peripheral cells arc polygonal lacking intercellular spaces. Vascular tissue consists of monarch to pentarch meristeles distributed thoughout the ground-tissue each surrounded by a uniscriale endodermis of thin-walled cells. Thin roots ofPlalanthera exhibit a typical central cylinder surrounded by a homogeneous cortex uninterrupted by meristeles; thicker roots show a central vascular cylinder and cortex in which meristeles are also present; in globoid root tubers there is no central cylinder, and the ground-tissue is replete with scattered meristeles. Because the central vascular cylinder in Platanthera gives rise to branches (meristeles), these represent components of a single vascular system and are not separate stelar entities as implied by the use of the term ‘polystele’.     

COMPARATIVE ANALYSES OF THE DINOFLAGELLATE FLAGELLAR APPARATUS. II. CERATIUM HIRUNDINELLA1

The three-dimensional structure of the flagellar apparatus in the gonyaulacoid dinoflagellate. Ceratium hirundinella var. furcoïdes (Schröder) Hub.-Pest. was determined using serial section electron microscopy. The flagellar apparatus is quite large and consists of several components. The two basal bodies nearly abut at their proximal ends and are separated by an angle of approximately 120° The broad longitudinal microtubular root extends from the cell's left edge of the longitudinal basal body and bends around the sulcal/cingular depression into the cell's left antapical horn. A transverse striated fibrous root is associated with the transverse basal body and a narrow electron dense extension is present along the anterior edge of the transverse basal body. This study revealed severa1 hitherto unreported fibrous components of the flagellar apparatus that link the various microtubular and fibrous components to themselves and to the two striated collars. A large striated fibrous connective links the two striated collars to one another. This fibrous connective is linked to another striated fibrous connective that originates from the longitudinal basal body and lies perpendicular to the longitudinal microtubular root. The readily identifiable and numerous components of the Ceratium flagellar apparatus are comparable to those of other dinoflagellates. The combined presence of well dpveloped striated collars, a striated collar connective, and a basal body angle of approximately 120° indicates that this flagellar apparatus is most like that described for Peridinioid dinoflagellates. Important similarities are also noticeable between this flagellar apparatus and that of Oxyrrhis marina.