scholarly journals A Review on Macroscopy, Microscopy and Pharmacological Activity of Cayratiatrifolia Linn.

2020 ◽  
Vol 8 (2) ◽  
pp. 90-95
Author(s):  
Kapil Sharma ◽  
Lavish Salvi ◽  
Ravi Gupta ◽  
Monika Meghani ◽  
Pradhuman Kumar Nagar ◽  
...  

Cayratiatrifolia (Linn.)Domin is a perennial climber, family Vitaceae, found in India, Asia and Australia. The plant is found in hilly regions as well as the hotter part of India from Jammu and Rajasthan to Assam. It is commonly known as fox grape in English, Amalbel, Ramchana in Hindi and Amlavetash in Sanskrit.   The plant has trifoliated leaves with (2-3cm) long petioles and ovate to oblong-ovate leaflets. Flowers are small greenish white and brown in colour. Fruits are fleshy, juicy, spherical, about 1 cm in diameter of dark purple or black colour.The stem composed of cork cells on the outer side and composed of small size sclerenchymatous cells. The cortex is wide and has parenchymatous cells. Numbers of sclereids are widely distributed in the cortex region. Cortex also shows the presence of calcium oxalate crystals.The leaf surface shows the stomata covered with guard cells followed by epidermis layer (Figure2A). Epidermal cells are rectangular, thin and straight walled cells. Stomata are anisocytic or unequal celled stomata, three subsidiary cells, one is smaller than other two. Leaf surface analysis also shows the presence of veins, vein islet and vein termination (Figure2B). Transverse section of leaf shows the epidermis layer followed by cuticle layer and vascular bundles (xylem and phloem).The leaf powder is pale green in color, with a characteristic odour and bitter taste.This plant also contains kaempferol, myricetin, quercetin, triterpenes and epifriedelanol. Whole plant of Cayratiatrifolia has been reported to contain yellow waxy oil, steroids/terpenoids, flavonoids, tannins. Plant shows the antioxidant, antidiabetic, antibacterial, antiviral and anticancer activity.    

2013 ◽  
Vol 20 (2) ◽  
pp. 135-144 ◽  
Author(s):  
Lin Meng ◽  
Peichun Mao

The micromorphological and anatomical characters of Elytrigia caespitosa (K.Koch) Nevski , E. intermedia (Host) Nevski × E. elongata (Host) Nevski, E. intermedia(Host) Nevski and  E. repens (L.) Desv. ex Nevski have been studied using Scanning Electron Microscope (SEM) to determine interspecific variation. The results show that the root transverse section consists of epidermis, cortex and stele. Two rings of vascular bundles and a central pith cavity appear in stem morphology. The leaves of  E. caespitosa have either single or twin, horse shoe-shaped short cells born along the costal zone of the upper epidermis, which lack prickle hairs and contain spherical or oblique-shaped papillae. In  E. intermedia, the parallel subsidiary cells are distributed on the upper epidermis, and there are no short cells in the leaves. Dome-shaped subsidiary cells appear on the upper epidermis of  E. intermedia × E. elongata and E. repens, but E. intermedia × E. elongata showes spot-shaped papillae, and its bulliform cells sank into the “hinge cells”. E. repens has no papillae, and its bulliform cells are not sunken into the mesophyll. Therefore, the differences in micromorphological characters on the upper epidermis of the leaf could be useful in classifying and determining phylogenetic relationships among the species.DOI: http://dx.doi.org/10.3329/bjpt.v20i2.17388Bangladesh J. Plant Taxon.  20(2): 135-144, 2013


Author(s):  
A. Sivanesan

Abstract A description is provided for Rosellinia bunodes. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On arrowroot, Artocarpus integer, avocado, banana, cacao, camphor, cassava, Centrosemapubescens, Cinchona, Citrus, coffee, Colocasia antiquorum, Crotalaria, Desmodium gyroides, Dryobalanops aromatica, Erythrina, ginger, Gliricidia, Grevillea robusta, Hibiscus rosa-sinensis, Holigarna longifolia, Indigofera, Inga laurina, Leucaena glauca, Litsea, pepper (black), Petiveria alliacea, Phyllanthus, rattan, rubber, Schleichera trijuga, tea, Tephrosia and yams. DISEASE: Black root rot, mainly of tropical and subtropical woody hosts; plurivorous but described mostly from cacao (Theobroma cacao), quinine (Cinchona spp.), coffee (Coffea spp.), rubber (Hevea brasiliensis) and tea (Camellia sinensis). Wilt and death of the whole plant or single branches may be the first signs of attack. At the collar the mycelial sheet is at first cream-white shading to purplish-black and may extend well above the soil surface in damp conditions. On the root surface the firm, black, branching strands are firmly applied and thicken into irregular knots. In the cortex the strands have a black periphery and white core; in the wood they appear thread-like and black or sometimes as dots in transverse section. In culture the mycelium is white, later buff with black strands. GEOGRAPHICAL DISTRIBUTION: Widespread in tropical America and also in Central African Republic, India (Nilgris, Maharashtra). Indonesia (Java, Sumatra), Malaysia (W.), Philippines. Sri Lanka (Ceylon) and Zaire Republic (CMI Map 358, ed. 2, 1970). Additional records not yet mapped are Honduras, Panama. TRANSMISSION: As mycelium from surface oreanic litter and woody debris.


1991 ◽  
Vol 4 (2) ◽  
pp. 391
Author(s):  
M Lazarides ◽  
J Lenz ◽  
L Watson

Clausospicula, a new monotypic genus from the Darwin and Gulf District, Northern Territory, Australia, is described and illustrated. Its diagnostic characters include cleistogamous spikelets, reduced panicles, racemes and spikelets, and pedicelled spikelets which are poorly developed and deciduous, or suppressed. Also, the glumes of the bisexual spikelet are awned and slightly keeled or without keels. A prominent feature is the extension of the peduncle into an appendage to which the callus of the bisexual spikelet is attached. The epidermis is notable for its distinct costal and intercostal zones, rectangular intercostal long-cells with tessellated, pitted cell walls, stomata inserted beneath the overlapping interstomatals and arranged in definite rows bordering the costal zones, the presence of macrohairs, narrow microhairs 39–46.5 µm long, silica-celllcork-cell pairs with dumbbell-shaped silica bodies costally and butterfly-shaped silica bodies intercostally. The transverse section shows a distinct midrib with the vascular bundles arranged in a conventional arc abaxially and colourless tissue adaxially, and a symmetrically ordered lamina. The primary vascular bundles are accompanied by sclerenchyma as girders abaxially and adaxially; the adaxial epidermis is extensively bulliform and the abaxial epidermis is of bulliform-like cells.


2020 ◽  
pp. 182-186
Author(s):  
G. Prabhakar ◽  
K. Shailaja ◽  
P. Kamalakar

The paper deals with a detailed investigation on the leaves of Maerua oblongifolia (Forssk.) A. Rich. which includes it’s morphological, anatomical and powder analysis. It is a low woody bushy under-shrub belonging to the family Capparaceae. The leaves are used in treatment of as fever, ear ache, stomach ache, skin infections, urinary calculii, diabetes mellitus, epilepsy, rigidity in lower limbs, and abdominal colic. The leaf amphistomatic, with mostly anamocytic, few tetracytic stomata. In transverse section of leaf is ribbed on either sides at midvein, epidermis one layered. Mesophyll differentiated into palisade and spongy tissues. Ground tissue of midvein differentiated into palisade, collenchyma and parenchyma. The midvien consists of one large oval shaped vascular bundles arranged are at the centre. Petiole in transverse section is circular adaxially small, grooved at centre and epidermis is having one layered, a single circular vascular bundle present at the centre, vascular bundle is enclosed by endodermis. The powder microscopic and organoleptic characters are also presented in this study. This study would helps as an appropriate source for authentification of the present studied drug.  


2016 ◽  
Vol 46 (2) ◽  
pp. 119-126 ◽  
Author(s):  
Ana Paula Ramos ARIANO ◽  
Ivone Vieira da SILVA

ABSTRACT Leaves have a variety of morphological and anatomical characters mainly influenced by climatic, edaphic and biotic factors. The aim of this study was to describe the anatomical leaf traits of Qualea parviflora from three phytophysiognomies. The studied phytophysiognomies were Amazon Savannah on rocky outcrops (ASR), Transition Rupestrian Cerrado (TRC), and Cerradão (CDA). Freehand sections of the leaf blade were made and stained with 0.5% astra blue and with basic fuchsin. From the adaxial and abaxial leaf surface, freehand paradermal sections were made for epidermis analysis. The Jeffrey´s method, with modifications, was used in the epidermis dissociation process. The samples from the TRC phytophysiognomy had relatively smaller ordinary epidermal cells, higher abundance of trichomes, and mesophyll with few intercellular spaces, in comparison to the other phytophysiognomies. The leaves from the ASR phytophysiognomy had higher stomatal index (SI = 21.02), and five to six layers of sclerenchyma surrounding the midrib vascular bundle. The secondary vascular bundles had thicker cell walls and the bundle sheath extended up to the epidermal tissue of both leaf sides. Leaves from the CDA phytophysiognomy had mesomorphic environmental traits, such as a thinner cuticle. It is concluded that trees from ASR and TRC phytophysiognomies have xeromorphic traits following the environmental conditions where they occur.


1992 ◽  
Vol 22 (10) ◽  
pp. 1441-1448 ◽  
Author(s):  
Daniel K. Struve ◽  
Robert J. Joly

One-year-old red oak seedlings (Quercusrubra L.) from three open-pollinated families were produced in 1 m tall containers during 1989. In spring 1990, the seedlings were either transplanted (which included pruning the main root to a 15-cm length) or not. Transplanted seedlings either received a 5-s basal dip in 20 mM indole-3-butyric acid or did not. The seedlings were placed in a greenhouse and harvested at the beginning of the first lag phase, at the beginning of elongation of the second growth flush, and 70 days after the beginning of the experiment. Root-pruning removed 42 to 50% of whole-plant dry weight. Transplanted seedlings had significantly reduced leaf surface area and began a second growth flush later than untransplanted seedlings. There were no treatment differences in CO2 assimilation rate on a per unit leaf surface area. Predawn xylem water potential in transplanted seedlings was lower than in untransplanted seedlings. Transplanted seedlings used less root and more shoot reserves to develop the first flush than untransplanted seedlings. Treating root-pruned seedlings with 20 mM indole-3-butyric acid did not significantly increase growth potential compared with untreated transplanted seedlings. For transplanted red oak, transplant shock seems to be mediated through reduced leaf surface area, which reduces whole-plant water use.


1937 ◽  
Vol 69 (4) ◽  
pp. 86-89
Author(s):  
T. D. A. Cockerell
Keyword(s):  
Red Eyes ◽  

Triepeolus helianthi Robertson. Lethbridge, Aug. 11 (G. A. Mail.) Described from Illinois, but known to be widely distributed.Triepeolus stricklandi n. sp.♀. Length about 8 mm.; black, including mandibles (except a dull red band in middle), antennae, tegulae (except red spot on outer side) and legs (except small joints of tarsi, which are red) ; eyes pale green, with a purplish suffusion below; pubescent markings pale cream-colour, pure white in region about antennae, the under side of abdomen without light markings; spurs black.


2012 ◽  
Vol 517 ◽  
pp. 112-117 ◽  
Author(s):  
Dong Sheng Huang ◽  
Ai Ping Zhou ◽  
Hai Tao Li ◽  
Yi Su ◽  
Guo Chen

Considering bamboo as a 2-phase natural composite made up of vascular bundles (reinforcement or fiber) and matrixes (ground tissues) on the scale of micromechanics. By test of bamboo specimens and analysis of microscopic images of their cross sections, the distribution of vascular bundles along the axial and radial of bamboo culm were investigated. The relations between tensile properties of bamboo and its distribution of vascular bundles were studied. The results show that the vascular bundles are graded distributing along the radius of bamboo culm. The volume fraction of vascular bundles is larger near the outside, and attenuates rapidly to about 40 percent of that at the location away from outer side about 1/3 thickness of bamboo culm, and than slowly reduces to 0 near the inner side of culm. In axial direction, the volume fraction of vascular bundles in the bottom culm is smaller than that in the middle culm where the volume fraction is less variation, and reaches the largest value at the top culm. The tensile moduli and strength of bamboo are linearly related to the volume fraction of vascular bundles. The tensile moduli and the strength of vascular bundle are largely grater than that of matrix. The stiffness and the strength of bamboo are mainly offered by vascular bundles.


In the fourth of this series of Memoirs (‘Phil. Trans.,' 1873, p. 377, et seq .) I described a remarkable plant under the name of Dictyoxylon Oldhamium ; I also gave reasons for substituting the late Mr. Gourlie ’s generic name of Lyginodendron for that of Dictyoxylon . In the same Memoir (p. 403) I referred to some petioles, to which I proposed to assign the name of Edraxylon ; but later researches demonstrated the necessity for abandoning this as a generic term and substituting for it the more comprehensive one of Rachiopteris aspera . In my Memoir, Part VI. ('Phil. Trans.,' 1874, Plate 2, p. 679, et seq .), I described this proposed Edraxylon under the name of Rachiopteris aspera . Certain similar features exhibited by the above two plants led me to remark in Memoir IV., p. 403, after showing that the Rachiopteris aspera was obviously the petiole of a Fern, “I think it far from impossible that these may prove to belong to Dictyoxylon ( Lyginodendron ) Oldhamium ; but since I have not yet succeeded in correlating them with any certainty, 1 shall add no more respecting them at present.” Since 1873 1 have accumulated a vast amount of material illustrative of the structure and relations of these two plants, and am now in a position to demonstrate that they respectively represent the stem and petiole of the same organism which proves to be a Fern. I was long under the conviction that the remarkable exogenous development of the stems of many of the Carboniferous Cryptogams, which I have so continuously demonstrated to exist, and which is now so universally recognised by Palæontologists, had no existence amongst Ferns. I have now to show that this development did exist amongst Ferns as well as amongst the arborescent Lycopods and Calamites, in which it is so conspicuous. Fig. 1 (Plate 12) is part of a transverse section of a stem or branch of Lyginodendron Oldhamium , in which a represents the medulla; b , the exogenous xylem zone; c , the place of the inner cortex, wanting in this specimen; d , one of the pairs of vascular bundles, so characteristic of the, cortex of this plant; e , the outermost cortex, composed, in transverse sections, of radiating bands of sclerenchyma, g , alternating with parenchymatous areas, f . At k, k we find two bundles of tracheids, like those at d , forming the centre of the cortical structures of a petiole of Rachiopteris aspera , i, i , which petiole is organically united to the cortex e of the Lyginodendron . The two bundles k, k are assuming the oblique relative positions seen in the similar bundles of the free petiole of R. aspera , represented in fig. 2. Other sections in my cabinet, similar to fig. 1, demonstrate the same facts, viz., that the pairs of bundles, fig. 1, d , which form so characteristic a feature of transverse sections of the middle cortex of Lyginodendrom Oldhamium , pass outwards, through the outer cortex, to become the tracheæal bundles of the petioles of the plant, and which petioles I had previously designated Rachiopteris aspera . I may state that my friend Graf Solms-Laubach, who has obtained numerous specimens of the Lyginodendron associated with others of Rachiopteris aspera from a locality on the continent, agrees with me in the conclusion at which I have arrived respecting their unity. The more perfect specimens of the Lyginodendron obtained during the last seventeen years have thrown yet further light upon those figured in 1873. In the latter, as at fig. 1, c, no traces of the middle bark were preserved; but examples from Halifax, for which I am indebted to my friends Mr. Cash and Mr. Spencer, of Halifax, have supplied what was wanting. Fig. 3 is a transverse section in which this inner cortex, c , is shown to consist of a zone of extremely delicate, thin-walled parenchymatous cells, scattered throughout which are numerous gum-canals, l . Three of these canals are represented, enlarged 250 diameters, in figs. 4 and 5, embedded in the thin-walled cells, c, c , of the cortex.


1999 ◽  
Vol 47 (5) ◽  
pp. 795 ◽  
Author(s):  
Geoffrey E. Burrows ◽  
Suzanne Bullock

Leaves of adult morphology from Wollemi pine(Wollemia nobilis W.G.Jones, K.D.Hill & J.M.Allen)possess a thick cuticle, sunken stomata, abundant hypodermal fibres, distinctpalisade and spongy mesophyll with most palisade development on the adaxialside, compartmented cells, resin canals, sclereids, and vascular bundles withtransfusion tissue and a fibre cap abaxial to the phloem. Stomata are presenton both leaf surfaces, although in greater density on the abaxial surface, andusually have an oblique orientation and four or five subsidiary cells. At thelight microscope level, Araucaria can be distinguishedfrom Agathis as it possesses unusual compartmented cellsin the mesophyll, while Agathis does not. In addition,most Agathis species are hypostomatic, while mostAraucaria species have stomata on both the abaxial andadaxial surfaces. Thus W. nobilis has a leaf anatomywhich has a greater similarity to Araucaria than toAgathis.


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