Layered cuticle

Crevasse breach in a levee on the bank of a river through which floodwater may flow. Crystalline Fe stable crystalline forms of Fe found in minerals such as goethite. Cutins lipid polyester polymers in vascular plant tissues which serve as a protective layer cuticle. 

The histological structure of wool fibre comprises consisting three layers the scaly covering layer (cuticle), the fibrous fibrillar layer (cortex) and medullary layer (medulla). Fig. 1 - 5 shows the diagarm of wool fibre showing fibre morphology... 

Cutin. Structural component of the outer lipophilic protective layer (cuticle) of the aerial parts of plants, especially leaves. Suberin serves similar functions in roots and bark. C. is a natural polyester, formed enzymatically from hydroxyfatty acids with 16 and 18 C atoms. o+Hydroxy- and dihydroxyfatty acids, e.g., 10,16-dihydroxypalmitic acid, as well as epoxy- and oxofatty acids, and a,o>-dicarboxylic acids are the main components of cutin. Cutinases (C.-cleaving enzymes) occur especially in pollen and in plant-pathogenic fungi, e.g., Fusarium solani (while rot in potatoes). 

Wool and hair have the most complex structures of any textile fibres. In the paper by Viney, fig. 1 shows how keratin proteins, of which there are more than one type, all having a complicated sequence of amino acids, assemble into intermediate filaments (IFs or microfibrils). But, as shown in Fig. 5a, this is only one part of the story. The microfibrils are embedded in a matrix, as shown in Fig. 5b. The keratin-associated proteins of the matrix contain substantial amounts of cy.stine, which cross-links molecules by -CH2-S-S-CH2- groups. Furthermore, terminal domains (tails) of the IFs, which also contain cystine, project into the matrix and join the cross-linked network. At a coarser scale, as indicated in Fig. 5c, wool is composed of cells, which are bonded together by the cell membrane complex (CMC), which is rich in lipids. As a whole, wool has a multi-component form, which consists of para-cortex, ortho-cortex, meso-cortex (not shown in Fig. 5a), and a multi-layer cuticle. In the para-and meso-cortex the fibril-matrix is a parallel assembly and the macrofibrils, if they are present, run into one another, but in the ortho-cortex the fibrils are assembled as helically twisted macrofibrils, which are clearly apparent in cross-section.s. 

Hurst (19) discusses the similarity in action of the pyrethrins and of DDT as indicated by a dispersant action on the lipids of insect cuticle and internal tissue. He has developed an elaborate theory of contact insecticidal action but provides no experimental data. Hurst believes that the susceptibility to insecticides depends partially on the cuticular permeability, but more fundamentally on the effects on internal tissue receptors which control oxidative metabolism or oxidative enzyme systems. The access of pyrethrins to insects, for example, is facilitated by adsorption and storage in the lipophilic layers of the epicuticle. The epicuticle is to be regarded as a lipoprotein mosaic consisting of alternating patches of lipid and protein receptors which are sites of oxidase activity. Such a condition exists in both the hydrophilic type of cuticle found in larvae of Calliphora and Phormia and in the waxy cuticle of Tenebrio larvae. Hurst explains pyrethrinization as a preliminary narcosis or knockdown phase in which oxidase action is blocked by adsorption of the insecticide on the lipoprotein tissue components, followed by death when further dispersant action of the insecticide results in an irreversible increase in the phenoloxidase activity as a result of the displacement of protective lipids. This increase in phenoloxidase activity is accompanied by the accumulation of toxic quinoid metabolites in the blood and tissues—for example, O-quinones which would block substrate access to normal enzyme systems. The varying degrees of susceptibility shown by different insect species to an insecticide may be explainable not only in terms of differences in cuticle make-up but also as internal factors associated with the stability of oxidase systems. 

In an alkaline solution, the cuticle—the outermost layer of a strand of hair—swells up, softens, and becomes rougher. The cuticle is made up of translucent, flattened cells that line the hair shaft like shingles on a roof. The cuticle gets rougher when the cells do not lay flat. When the raised cuticle cells of one piece of hair get stuck on the raised cuticle cells of another piece of hair, the hair tangles. The raised cells also reflect light differently than smooth, flat cells, making the hair appear dull. 

Consistent with the definition of terms adopted for the discussion in this series of papers of integral phases of the residue studies being conducted by the Division of Entomology, University of California Citrus Experiment Station (2, 13-15), the following distinctions are noted Residues may be specified as pretreatment, posttreatment, harvest, or ultimate. The latter refers to the residue on or in foodstuffs, whether fresh or processed, at the time of consumption (2, 13). The location of residues with reference to fruit parts may be extra-surface (external to the cuticle) or subsurface. Subsurface residues may be differentiated with reference to actual location as cuticular residues or specified intracarp residues. Residues in the cuticular layers or in any of the cellular structures or matrices are herein indicated as subsurface (penetrated) residues (2, 13). 

Drosophila Ddc is expressed primarily in the CNS and the hypoderm, the epithelial layer of the fly that secretes the cuticle. In the CNS, Ddc is expressed in a small subset of neurons that produce either dopamine or serotonin (Budnik and White, 1988 Valles and White, 1988). In the hypoderm, Ddc expression leads to synthesis of dopamine, which is further metabolized into quinones that have a vital function in the cross-linking, hardening, and pigmentation of the fly cuticle (Wright, 1987). The developmental profile of DDC activity in these two tissues is quite different (Hirsh, 1986). DDC is first detected during late embryo-... 

A thin outer, sometimes hairy layer, known as the epidermis or cuticle... 

Fig. 9.1. Transmission electron micrographs of parasitic nematode cuticles in transverse section. The structurally distinct layers and the underlying hypodermal syncytia are indicated. Nematodes depicted are the infective larval stage of the canid parasite Toxocara canis and the fourth larval stage of the human filarial parasite Brugia malayi.

Late lethargus is characterized by the formation of the new cuticle, which arises externally to the cell membrane of the hypodermis, and thus represents a true extracellular matrix. The epicuticular and cortical layers are the first to be formed and these layers are enriched in the highly... 

Plants were probably the first to have polyester outerwear, as the aerial parts of higher plants are covered with a cuticle whose structural component is a polyester called cutin. Even plants that live under water in the oceans, such as Zoestra marina, are covered with cutin. This lipid-derived polyester covering is unique to plants, as animals use carbohydrate or protein polymers as their outer covering. Cutin, the insoluble cuticular polymer of plants, is composed of inter-esterified hydroxy and hydroxy epoxy fatty acids derived from the common cellular fatty acids and is attached to the outer epidermal layer of cells by a pectinaceous layer (Fig. 1). The insoluble polymer is embedded in a complex mixture of soluble lipids collectively called waxes [1], Electron microscopic examination of the cuticle usually shows an amorphous appearance but in some plants the cuticle has a lamellar appearance (Fig. 2). 

The cuticle, being attached to the epidermal cells via a pectinaceous layer, can be released by disruption of this layer by chemicals such as ammonium oxalate/oxalic acid or by pectin-degrading enzymes. After treatment of the recovered cuticular layer with carbohydrate-hydrolyzing enzymes to remove the remaining attached carbohydrates, the soluble waxes can be removed by ex-... 

The conquest of the land by plants necessitated the development of a coating, the cuticle, that would reduce water loss. Suberin and cutin vary in their proportion of fatty acids, fatty alcohols, hydroxyfatty acids, and dicarboxylic acids. The cuticle is synthesized and excreted by the epidermis of aerial portions of the plant, such as the primary stems, leaves, flower organs, and fruits. The two major hydrophobic layers that contribute to the cuticle are composed of phenolic molecules combined with lipid polymers. Cutin is a polymer found in the outer cell wall of the epidermis, which is... 

These gas- and water-impermeable cell layers protect the plant from desiccation, but they also hamper the uptake of carbon dioxide necessary for photosynthesis and oxygen necessary for respiration. Specialized tissues have evolved to allow passive (lenticels) and active (guard cells) modification of the permeability of the external cuticle to gas exchange. 

Epidermal cells Tabular are layered sheets on surfaces of leaves and young roots, stems, flowers, fruits, seeds, ovules Secrete the fatty substance, cutin, which forms a protective layer, the cuticle cuticle covered by an epicuticular wax... 

This method gives a bright fluorescence of callose but also a side effect due to the presence of chlorophyll. Chlorophyll dispersed in the specimen yields a red fluorescence all around the tissue, especially a red layer on the surface of the organs due to chlorophyll deposition in any lipid substances, such as a cuticle. 

Niche The section of the environment with which a particular property of the chemical product interacts is referred to as niche. For example, a pesticide can have as the environment the plant, the atmosphere, and the human beings. The pesticide interacts with the environment through its properties. There are different kinds of interaction depending on the niche. For example, some properties such as the contact area depend on the surfactant characteristics and the surface of the leaf. The niche is the surface of the leaf. The absorption of the pesticide depends on the characteristics of the layers, like the cuticle [25], In this case, the niche consists of the layers of the plant s leaves. Also, the diffiisivity of the active product in the layers of the plant leaves corresponds to a property that depends on the environment-product interaction. Some other pesticide properties, such as solubility of the active agent in the solvent, do not depend on the environment. 

Terrestrial BMOs have also been widely used for monitoring environmental contaminants. In particular, the lipid-like waxy cuticle layer of various types of plant leaves has been used to monitor residues of HOCs in the atmosphere. However, some of the problems associated with aquatic BMOs apply to terrestrial BMOs as well. For example, Bohme et al. (1999) found that the concentrations of HOCs with log KoaS < 9 (i.e., those compounds that should have attained equilibrium) varied by as much as 37-fold in plant species, after normalization of residue concentrations to levels in ryegrass (Lolium spp.). These authors suggested that differences in cuticular wax composition (quality) were responsible for this deviation from equilibrium partition theory. Other characteristics of plant leaves may affect the amount of kinetically-limited and particle-bound HOCs sampled by plant leaves but to a lesser extent (i.e., <4-fold), these include age, surface area, topography of the surface, and leaf orientation. 

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