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Epidermal Cell Walls (epidermal + cell_wall)
Selected AbstractsHost and non-host pathogens elicit different jasmonate/ethylene responses in ArabidopsisTHE PLANT JOURNAL, Issue 5 2004Laurent Zimmerli Summary Arabidopsis does not support the growth and asexual reproduction of the barley pathogen, Blumeria graminis f. sp. hordei Bgh). A majority of germlings fail to penetrate the epidermal cell wall and papillae. To gain additional insight into this interaction, we determined whether the salicylic acid (SA) or jasmonate (JA)/ethylene (ET) defence pathways played a role in blocking barley powdery mildew infections. Only the eds1 mutant and NahG transgenics supported a modest increase in penetration success by the barley powdery mildew. We also compared the global gene expression patterns of Arabidopsis inoculated with the non-host barley powdery mildew to those inoculated with a virulent, host powdery mildew, Erysiphe cichoracearum. Genes repressed by inoculations with non-host and host powdery mildews relative to non-inoculated control plants accounted for two-thirds of the differentially expressed genes. A majority of these genes encoded components of photosynthesis and general metabolism. Consistent with this observation, Arabidopsis growth was inhibited following inoculation with Bgh, suggesting a shift in resource allocation from growth to defence. A number of defence-associated genes were induced during both interactions. These genes likely are components of basal defence responses, which do not effectively block host powdery mildew infections. In addition, genes encoding defensins, anti-microbial peptides whose expression is under the control of the JA/ET signalling pathway, were induced exclusively by non-host pathogens. Ectopic activation of JA/ET signalling protected Arabidopsis against two biotrophic host pathogens. Taken together, these data suggest that biotrophic host pathogens must either suppress or fail to elicit the JA/ET signal transduction pathway. [source] Visualisation of the uptake of two model xenobiotics into bean leaves by confocal laser scanning microscopy: diffusion pathways and implication in phloem translocationPEST MANAGEMENT SCIENCE (FORMERLY: PESTICIDE SCIENCE), Issue 5 2004Dr Zhiqian Liu Abstract The diffusion of two fluorescent dyes, Oregon Green 488 (Oregon Green) and Rhodamine B into the leaves of broad bean (Vicia faba L) plants was studied to simulate the foliar uptake process of pesticides. The uptake rate of these model xenobiotics into bean foliage was measured using a standard leaf surface wash-off method. Diffusion into leaf tissues was visualised in vivo by confocal laser scanning microscopy (CLSM). The moderately lipophilic dye (Rhodamine B) showed faster uptake than the hydrophilic one (Oregon Green), despite the former being a larger molecule. While no distinct channels or domains for preferential entry of any of the dyes could be detected in the cuticle layer by CLSM, two different diffusion patterns were identified for the movement of these two dyes after traversing the cuticle. Upon desorption from the cuticle, Rhodamine B diffused extensively into the vacuole of the epidermal cells. Further transport of this dye from the epidermal cells to the mesophyll cells was not observed. In contrast, Oregon Green was found in the epidermal cell walls and cytoplasm, and was also present in the mesophyll cells. Examination of the petioles of the treated leaves revealed that, once absorbed, Oregon Green moved readily out of the treated leaf, whereas Rhodamine B did not show any phloem translocation. It is proposed that these two different diffusion characters may be responsible for the contrasting phloem mobility of the two xenobiotics. The results are discussed in relation to the current knowledge on the uptake, translocation and efficacy of pesticides as influenced by their properties. Copyright © 2004 Society of Chemical Industry [source] Leaf, floret and seed infection of wheat by Pyrenophora semeniperdaPLANT PATHOLOGY, Issue 4 2003M. A. Campbell Infection processes of Pyrenophora semeniperda on seedling and adult wheat leaves and wheat ears were investigated. Almost 100% germination of conidia occurred on seedling leaves, compared with 20,30% on adult leaves. Appressoria formed over the anticlinal epidermal cell walls and haloes always accompanied infection. Sometimes papillae formed within the leaves as a resistance mechanism. Infection hyphae ramified through the intercellular spaces of the mesophyll resulting in cellular disruption. The infection processes on floral tissues were similar to those observed on leaves; however, no infection occurred on anther, stigmatic or stylar tissues. Infection of ovarian tissue occurred both with and without appressoria formation. Hyphae grew mainly in the epidermal layers and appeared unable to breach the integumental layer as no growth was observed in endosperm or embryo tissues. The optimum dew period temperature for conidial germination was 23·6°C, compared with 19·9°C for lesion development, 20·4°C for the production of infection structures on seedling leaves and 23·7°C for floret infection. Leaf disease development occurred in a logistic manner in response to dew period, with maximum infection observed after 21 h compared with > 48 h in seeds. An initial dark phase during the dew period was necessary for infection and temperature after the dew period had an effect, with significantly more numerous and larger lesions being formed at 15°C compared with 30°C. Seedling leaves were found to be more susceptible than older leaves, under both field and controlled environment conditions. Infection of wheat seeds following inoculation of ears, or after harvest burial of inoculated disease-free seeds, was demonstrated. In the latter, 3-week-old seedlings were slightly stunted, whereas older plants were unaffected. The apparent unimportance of this plant pathogen as a cause of leaf disease in relation to its poor adaptation to dew periods and dew period temperature is discussed, along with the importance of its seed borne characteristics. [source] Cuticle micromorphology of leaves of Pinus (Pinaceae) from Mexico and Central AmericaBOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 4 2001SUNG SOO WHANG Cuticle micromorphology of 34 taxa of Pinus from Mexico and Central America was studied with scanning electron microscopy, and leaf morphology was described. In total, 29 characters, 22 from the inner cuticular surfaces and seven from the outer, were described in detail. These characters have value either for testing infragenerie classifications or for identifying individual taxa. Characters relating to the periclinal wall texture of the epidermal cells, the shape and degree of development of the anticlinal walls of the epidermal cells, the basal and apical shapes of anticlinal epidermal cell walls, the continuity of the epidermal cells, the size ratio of the polar to lateral subsidiary cells, the grooves on subsidiary cells, the cuticular flanges between guard and subsidiary cells, the groove near the bristles and the elevation of the Florin ring ridge and striations on the Florin ring are particularly useful for infrageneric classification. The agreement between these characters and infrageneric classifications is discussed. Characters relating to the end wall shapes of the epidermal cells, the relative length of epidermal cells, the shape of the stomatal apparatus, the texture of guard and lateral subsidiary cell surfaces, the polar extensions, the number of subsidiary cells and epidermal cell layers between stomatal rows, the integrity of stomatal rows, cell numbers between stomata in a row, cuticular flanges between guard cells, bristle flanges and surface textures, epicuticular waxes, striations on Florin rings and stomatal shapes, contain some important information for identifying Mexican pines. The distribution of the states of each character is compared with that of the Asian pines. Cuticular characters are used to help determine the affinities of taxonomically difficult taxa. [source] Phytoliths of Indian grasses and their potential use in identificationBOTANICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2000S. KRISHNAN Phytoliths are amorphous silicon dioxide (SiO2.nH2O) inclusions abundant in leaves, in-ternodes and glumes in members of Poaceae. They may occur as inclusions filling the entire lumen of the silica cells, bulliform cells and trichomes or may be part of the outer epidermal cell walls. Since phytoliths are resistant to fungal or animal digestive juices, a large quantity of phytoliths accumulate in the soil where grasses grow. Compared with the pollen grains of grasses which tend to be uniform, phytoliths vary in sue and morphology and can be of value in identification at different taxonomic levels and in the dating of past vegetation. The size and shape of phytoliths of about 100 species of grasses from Tamil Nadu, India, have been determined. Silica bodies were observed either after isolation or in cleared leaf blades. Size and shape of phytoliths were determined under a microscope or from micrographs of the specimens. Size and shape can be used to assign the phytoliths to their respective subfamilies and to distinguish some of the grasses at the generic level. Drawings of silica cells and an identification key are provided for 80 species. [source] | ||||||||||