Effect of Media pH on Growth and Leaf Tissue Element Concentration of ‘Vidal blanc’ and ‘Norton’ Grape Cultivars

2011 ◽  
Vol 11 (4) ◽  
pp. 332-341 ◽  
Author(s):  
Maru Kipleting Kering ◽  
Martin Kaps
HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 547g-547
Author(s):  
Gary C. Pavlis ◽  
Joseph A. Fiola

Downy Mildew, Plasmopara viticola, causes major damage and economic loss to many wine grape cultivars grown in the Northeast. The purpose of this experiment was to test the efficacy of Vossen Blue (VB; iron pigment) in association with fungicides for the control of Downy Mildew disease of wine grapes in New Jersey. The experimental plot was a planting of Chancellor (10th leaf). Treatments (applied via back-pack sprayer) included no fungicide (NF), full fungicide (FF) (RCE commercial recs. half fungicide (HF), FF + 8%VB (FF8), HF + 8% VB (HF8), 88V B. Subjective (l-9) disease score for leaf tissue showed no statistical difference between the FF, FF8, HF and HF8 treatments however all showed superior Downy Mildew control to the 8% VB and the no fungicide control. Yield data indicated that the FF8 treatment resulted in higher yield (p is ≤ 0.01) than FF, HF and HF8. The NF and 8VB treatments resulted in the lowest yield. Compared to normal full fungicide, superior Downy Mildew control on the fruit was achieved by adding VB to full fungicide. These results are consist with previous experiments conducted on Seyval Blanc.


1987 ◽  
Vol 65 (8) ◽  
pp. 1643-1646 ◽  
Author(s):  
P. M. Miller

Photosynthetic rates, dry moss accumulation, leaf number per shoot, stem length, and tissue element concentrations were measured in Vaccinium vitis-idaea growing in tussock tundra at Toolik Lake, Alaska. Manganese concentrations of 6 800 – 12 300 μg/g dry mass in leaf tissue of V. vitis-idaea did not affect photosynthetic rates, dry mass, or leaf number when compared with plants containing 18–1500 μg manganese/g dry mass. Tissue analysis indicated possible substitution of manganese for magnesium and inhibition of uptake and (or) translocation of calcium, iron, manganese, silicon, and aluminum. High concentrations of calcium and the high correlation between manganese and silicon concentrations suggest that these elements may play a role in manganese tolerance observed in V. vitis-idaea.


Author(s):  
O. E. Bradfute ◽  
R. E. Whitmoyer ◽  
L. R. Nault

A pathogen transmitted by the eriophyid mite, Aceria tulipae, infects a number of Gramineae producing symptoms similar to wheat spot mosaic virus (1). An electron microscope study of leaf ultrastructure from systemically infected Zea mays, Hordeum vulgare, and Triticum aestivum showed the presence of ovoid, double membrane bodies (0.1 - 0.2 microns) in the cytoplasm of parenchyma, phloem and epidermis cells (Fig. 1 ).


Author(s):  
Karen K. Baker ◽  
David L. Roberts

Plant disease diagnosis is most often accomplished by examination of symptoms and observation or isolation of causal organisms. Occasionally, diseases of unknown etiology occur and are difficult or impossible to accurately diagnose by the usual means. In 1980, such a disease was observed on Agrostis palustris Huds. c.v. Toronto (creeping bentgrass) putting greens at the Butler National Golf Course in Oak Brook, IL.The wilting symptoms of the disease and the irregular nature of its spread through affected areas suggested that an infectious agent was involved. However, normal isolation procedures did not yield any organism known to infect turf grass. TEM was employed in order to aid in the possible diagnosis of the disease.Crown, root and leaf tissue of both infected and symptomless plants were fixed in cold 5% glutaraldehyde in 0.1 M phosphate buffer, post-fixed in buffered 1% osmium tetroxide, dehydrated in ethanol and embedded in a 1:1 mixture of Spurrs and epon-araldite epoxy resins.


Author(s):  
R.H.M. Cross ◽  
C.E.J. Botha ◽  
A.K. Cowan ◽  
B.J. Hartley

Senescence is an ordered degenerative process leading to death of individual cells, organs and organisms. The detection of a conditional lethal mutant (achloroplastic) of Hordeum vulgare has enabled us to investigate ultrastructural changes occurring in leaf tissue during foliar senescence.Examination of the tonoplast structure in six and 14 day-old mutant tissue revealed a progressive degeneration and disappearance of the membrane, apparently starting by day six in the vicinity of the mitochondria associated with the degenerating proplastid (Fig. 1.) where neither of the plastid membrane leaflets is evident (arrows, Fig. 1.). At this stage there was evidence that the mitochondrial membranes were undergoing retrogressive changes, coupled with disorganization of cristae (Fig. 2.). Proplastids (P) lack definitive prolamellar bodies. The cytoplasmic matrix is largely agranular, with few endoplasmic reticulum (ER) cisternae or polyribosomal aggregates. Interestingly, large numbers of actively-budding dictysomes, associated with pinocytotic vesicles, were observed in close proximity to the plasmalemma of mesophyll cells (Fig. 3.). By day 14 however, mesophyll cells showed almost complete breakdown of subcellular organelle structure (Fig. 4.), and further evidence for the breakdown of the tonoplast. The final stage of senescence is characterized by the solubilization of the cell wall due to expression and activity of polygalacturonase and/or cellulose. The presence of dictyosomes with associated pinocytotic vesicles formed from the mature face, in close proximity to both the plasmalemma and the cell wall, would appear to support the model proposed by Christopherson for the secretion of cellulase. This pathway of synthesis is typical for secretory glycoproteins.


Author(s):  
William P. Sharp ◽  
Robert W. Roberson

The aim of ultrastructural investigation is to analyze cell architecture and relate a functional role(s) to cell components. It is known that aqueous chemical fixation requires seconds to minutes to penetrate and stabilize cell structure which may result in structural artifacts. The use of ultralow temperatures to fix and prepare specimens, however, leads to a much improved preservation of the cell’s living state. A critical limitation of conventional cryofixation methods (i.e., propane-jet freezing, cold-metal slamming, plunge-freezing) is that only a 10 to 40 μm thick surface layer of cells can be frozen without distorting ice crystal formation. This problem can be allayed by freezing samples under about 2100 bar of hydrostatic pressure which suppresses the formation of ice nuclei and their rate of growth. Thus, 0.6 mm thick samples with a total volume of 1 mm3 can be frozen without ice crystal damage. The purpose of this study is to describe the cellular details and identify potential artifacts in root tissue of barley (Hordeum vulgari L.) and leaf tissue of brome grass (Bromus mollis L.) fixed and prepared by high-pressure freezing (HPF) and freeze substitution (FS) techniques.


Author(s):  
D.A. Palmer ◽  
C.L. Bender

Coronatine is a non-host-specific phytotoxin produced by several members of the Pseudomonas syringae group of pathovars. The toxin acts as a virulence factor in P. syringae pv. tomato, allowing the organism to multiply to a higher population density and develop larger lesions than mutant strains unable to produce the toxin. The most prominent symptom observed in leaf tissue treated with coronatine is an intense spreading chlorosis; this has been attributed to a loss of chlorophylls a and b in tobacco. Coronatine's effects on membrane integrity and cell ultrastructure have not been previously investigated. The present study describes changes in tomato leaves in response to treatment with purified coronatine, infection by a coronatine-producing strain of P. syringae pv. tomato, and infection by a cor" mutant.In contrast to H2O-treated tissue, coronatine-treated tissue showed a diffuse chlorosis extending approximately 5 mm from the inoculation site. Leaf thickness, cell number, and cell dimensions were similar for both healthy and coronatine-treated, chlorotic tissue; however, the epidermal cell walls were consistently thicker in coronatine-treated leaves (Figs, la and lb).


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