Structure and development of the sieve-cell protoplast in leaf veins ofWelwitschia

PROTOPLASMA ◽  
1973 ◽  
Vol 76 (1) ◽  
pp. 1-21 ◽  
Author(s):  
Ray F. Evert ◽  
Chris H. Bornman ◽  
Valerie Butler ◽  
Margaret G. Gilliland
1975 ◽  
Vol 53 (22) ◽  
pp. 2589-2597 ◽  
Author(s):  
H. H. Edwards

M1-a-mediated resistance in barley to invasion by the CR3 race of Erysiphe graminis f. sp. hordei does not occur in every host cell with the same speed and severity. In some cells ultrastructural changes within the host cell as a result of resistance will occur within 24 h after inoculation, whereas in other cells these changes may take up to 72 h. In some cells the ultrastructural changes are so drastic that they give the appearance of a hypersensitive death of the host cell, whereas in other cells the changes are very slight. In any case, at the end of these changes the fungus ceases growth. The ultrastructural changes occur in penetrated host epidermal cells as well as non-infected adjacent epidermal and mesophyll cells.The following ultrastructural changes have been observed: (1) an electron-dense material which occurs either free in the vacuole or adhering to the tonoplast (the material is granular or in large clumps); (2) an increased electron density of the host cytoplasm and nucleus; (3) a breakdown of the tonoplast so that the cytoplasmic constituents become dispersed throughout the cell lumen; and (4) the deposition of papillar-like material in areas other than the penetration site. The first three changes take place within the host cell protoplasts and are directly attributable to the gene M1-a. These changes are typical of stress or incompatibility responses and thus M1-a appears to trigger a generalized incompatibility response in the presence of race CR3. The papillar-like material occurs outside the host cell protoplast in the same manner as the papilla and probably is not directly attributable to M1-a.


AoB Plants ◽  
2020 ◽  
Vol 12 (5) ◽  
Author(s):  
Wanli Zhao ◽  
Peili Fu ◽  
Guolan Liu ◽  
Ping Zhao

Abstract Emergent aquatic plants mostly occur in shallow waters and root in bottom substrates, but their leaves emerge from the water surface and are thus exposed to air, similar to the leaves of terrestrial plants. Previous studies have found coordination between leaf water supply and demand in terrestrial plants; however, whether such a coordination exists in emergent aquatic plants remains unknown. In this study, we analysed leaf veins and stomatal characteristics of 14 emergent aquatic and 13 terrestrial monocotyledonous herb species (EMH and TMH), with 5 EMH and 8 TMH belonging to Poaceae. We found that EMH had significantly higher mean leaf area, leaf thickness, stomatal density, stomatal number per vein length and major vein diameter, but lower mean major vein length per area (VLA) and total VLA than TMH. There was no significant difference in stomatal length, minor VLA and minor vein diameter between the two groups. Stomatal density and total VLA were positively correlated among the EMH, TMH, as well as the 8 Poaceae TMH species, but this correlation became non-significant when data from both the groups were pooled. Our results showed that the differences in water supply between emergent aquatic and terrestrial plants modify the coordination of their leaf veins and stomatal traits.


PROTOPLASMA ◽  
1994 ◽  
Vol 179 (1-2) ◽  
pp. 83-94 ◽  
Author(s):  
Anne-Marie Rusig ◽  
H. Le Guyader ◽  
G. Ducreux
Keyword(s):  

Plant Disease ◽  
2005 ◽  
Vol 89 (4) ◽  
pp. 432-432 ◽  
Author(s):  
P. Jimenez ◽  
T. A. Zitter

In early August 2004, pumpkin and zucchini squash (Cucurbita pepo) plants grown in conventional and organic commercial operations in Orange and Dutchess counties, respectively, showed spindle-shaped lesions on vegetative tissues and silver russeting and spots on fruit, typical of Plectosporium blight. Approximately 20% of pumpkin fruit were affected at this early time in yield development, while the zucchini planting had been abandoned due to disease. Symptomatic pieces of stem, petioles, and main leaf veins were excised, surface disinfected with 0.5% sodium hypochlorite, placed on one-quarter-strength potato dextrose agar, and incubated at 21°C with a 12-h photoperiod. Pale pink colonies with pinkish, hyaline, aerial mycelium developed from the tissues. When examined microscopically, simple and branched conidiophores with apical phialides were observed, as well as non- and one-septate ellipsoidal to slightly curved conidia that measured 7.5 to 13.0 × 2.5 to 3.3 μm. The fungus fits the description of Plectosporium tabacinum (van Beyma) M.E. Palm, W. Gams, & H.I. Nirenberg (synonyms Microdochium tabacinum (von Arx, 1984) and Fusarium tabacinum (Gams & Gerlagh, 1968) (1). Pathogenicity was tested on 10 seedlings each of pumpkin, zucchini, gourd (C. pepo), winter squash (C. moschata), and cucumber (Cucumis sativa). Plants were spray inoculated at the three true-leaf stage with a spore suspension at 104 conidia/ml in water with 1% gelatin. Plants were held overnight in a moist chamber and then transplanted into 12-cm-diameter pots and kept in the greenhouse for the rest of the experiment. P. tabacinum was reisolated from all inoculated plants which completes Koch's postulates. Symptoms were noted 3 days after inoculation on pumpkin, zucchini, and gourd, with typical spindle-shaped lesions on the main stem, petioles, and main leaf veins (2). Symptoms developed after 1 week on winter squash, and lesions were mostly concentrated on the older portion of the stem with occasional lesions on the petiole and main leaf veins. Symptoms on cucumber, however, did not develop until 2 weeks after inoculation and appeared as an inconspicuous line of coalesced lesions on the ridges of the main stem only. These symptoms could easily be misidentified as physical abrasions from handling or from wind scarring. These results confirm the high susceptibility of C. pepo species, and indicate that other cucurbits are susceptible, albeit at a lower level. To our knowledge, this is the first report of P. tabacinum in New York. A voucher specimen has been deposited in the Cornell Plant Pathology Herbarium (Accession No. CUP 67504). References: (1) M. E. Palm et al. Mycologia 87:397, 1995; (2) T. A. Zitter. Microdochium blight. Page 28 in: Compendium of Cucurbit Diseases. T. A. Zitter, D. L. Hopkins, and C. E. Thomas, eds. The American Phytopathological Society, St. Paul, MN, 1996.


Nature ◽  
2014 ◽  
Vol 515 (7527) ◽  
pp. 352-353 ◽  
Author(s):  
María C. Martí ◽  
Alex A. R. Webb
Keyword(s):  

Plant Disease ◽  
2014 ◽  
Vol 98 (12) ◽  
pp. 1709-1716 ◽  
Author(s):  
Jayme Garcia Arnal Barbedo

A method is presented to detect and quantify leaf symptoms using conventional color digital images. The method was designed to be completely automatic, eliminating the possibility of human error and reducing time taken to measure disease severity. The program is capable of dealing with images containing multiple leaves, further reducing the time taken. Accurate results are possible when the symptoms and leaf veins have similar color and shade characteristics. The algorithm is subject to one constraint: the background must be as close to white or black as possible. Tests showed that the method provided accurate estimates over a wide variety of conditions, being robust to variation in size, shape, and color of leaves; symptoms; and leaf veins. Low rates of false positives and false negatives occurred due to extrinsic factors such as issues with image capture and the use of extreme file compression ratios.


Author(s):  
J. L. Mulder

Abstract A description is provided for Ramularia gossypii. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Gossypium spp. DISEASE: Grey mildew of cotton (Gossypium). The symptoms occur chiefly on the older leaves as the plants mature. The spots are hypophyllous, rarely amphigenous, pale at first, becoming darker, (1-) 3-4 (-10) mm diam., angular, irregular in shape, limited by the leaf veins; conidia in profusion give a frosted appearance to the spots. GEOGRAPHICAL DISTRIBUTION: Widespread with hosts (CMI Map 260, ed. 2, 1967). TRANSMISSION: No specific studies reported.


Phytotaxa ◽  
2019 ◽  
Vol 427 (4) ◽  
pp. 239-248
Author(s):  
FRANK ARROYO ◽  
ÁLVARO J. PÉREZ ◽  
ALEX DAHUA MACHOA ◽  
DAVID A. NEILL ◽  
ALONDRA SALOME ORTEGA-PEÑA ◽  
...  

Magnolia napoensis, a new species from the Amazonian lowlands of Ecuador and Peru is described and illustrated. This species belongs to subsection Talauma; it is similar to M. rimachii in leaf shape but differs from the latter in being taller with a larger diameter and having fewer lateral leaf veins, more numerous hypsophylls, larger flowers, longer outer petals, more numerous stamens and fruits ovoid and ribbed vs. subglobose and smooth. The new species differs from M. neillii by its leaves with fewer lateral veins, glabrous petioles and terminal internodes, more numerous hypsophylls, fewer stamens and ovoid fruits of smaller size, with fewer carpels. Magnolia napoensis is assessed as endangered (EN B2ab(iii)) in accordance with the IUCN criteria.


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