Ultrastructure of pit membrane dissolution and movement of Xylella fastidiosa through pit membranes in petioles of Vitis vinifera

Botany ◽  
2010 ◽  
Vol 88 (6) ◽  
pp. 596-600 ◽  
Author(s):  
E. Ann Ellis ◽  
George Ray McEachern ◽  
Samantha Clark ◽  
B. Greg Cobb

Xylella fastidiosa is the causative agent in Pierce’s disease (PD) in Vitis vinifera L. (grape) vines. Xylella fastidiosa colonizes and disseminates itself from one xylem element to another by dissolution and breach of pit membranes. These studies on naturally infected V. vinifera grown under vineyard conditions document by transmission electron microscopy that there is dissolution and breach of pit membranes by X. fastidiosa in vertical and lateral colonization in PD. These processes were documented in two cultivars of V. vinifera: ‘Syrah’ and ‘Cabernet Sauvignon.’

IAWA Journal ◽  
2010 ◽  
Vol 31 (2) ◽  
pp. 227-240 ◽  
Author(s):  
María Luján Luna ◽  
Gabriela Elena Giudice ◽  
María Alejandra Ganem ◽  
Elías Ramón de la Sota

The structure of root and rhizome tracheary cells of Asplenium spp. (Filicales, Pteridophyta) growing in NW Argentina was studied using light microscopy (LM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). In all cases, tracheary cells consisted of tracheids with various facets, mainly with scalariform pitting. With SEM, intertracheary pit membranes appeared smooth and non porose in most cases. In some instances, porose or web-like to thread-like pit membranes were noticed in rhizome tracheids. Under TEM secondary walls displayed a smooth and uniform appearance. Pit membranes showed a variation in thickness in presumed association with their maturation stage. More mature tracheary cells showed pit membranes with a mesh-like aspect and visible openings or pores. These characteristics are attributed to pit membrane hydrolysis, which facilitates water transport among tracheary cells.


IAWA Journal ◽  
2016 ◽  
Vol 37 (3) ◽  
pp. 402-419
Author(s):  
Jong Sik Kim ◽  
Geoffrey Daniel

Although there is considerable information on the chemistry of bordered intervessel pit membranes, little is known on the pit membrane chemistry of other pit types in hardwoods. This study investigated distribution of phenolic compounds, pectins and hemicelluloses in different mature pit membranes of English oak xylem using transmission electron microscopy coupled with cytochemistry and immunocytochemistry. Mature bordered intertracheid (vasicentric)- and tracheid-vessel pits showed presence of xyloglucan and heteromannan (hemicelluloses) epitopes across the pit membrane (except for the annulus regions) with differences in amounts of epitopes between earlywood (EW) and latewood (LW). In contrast, pectin epitopes were detected only in the annulus regions of pit membranes. Unlike bordered pits, half-bordered (tracheary-parenchyma pits) and simple (parenchyma pits) pit membranes were rich in pectin epitopes but lacked heteromannan epitopes, indicating difference in pit membrane chemistry between pit types. Distribution of phenolic compounds also differed between pit types and between EW and LW. LW also showed great variations in distribution of phenolic compounds between vessels. Together, this study demonstrates that there are great variations in pit membrane chemistry between pit types and between EW and LW in English oak xylem.


Holzforschung ◽  
1999 ◽  
Vol 53 (4) ◽  
pp. 341-346 ◽  
Author(s):  
Adya Singh ◽  
Bernard Dawson ◽  
Robert Franich ◽  
Faye Cowan ◽  
Jeremy Warnes

Summary The woods of Alder and Eucalypt were examined by light microscopy before and after a chemical treatment by the Indurite process to increase the hardness of the wood. The pattern of wood cell impregnation for Alder differed significantly from Eucalypt in some respects. In Alder wood all cell types eg. vessels, fibres and rays, were impregnated in similar proportions. In comparison, in Eucalypt wood the impregnation material was largely confined to ray cells and the lumina of vessels; other cell types were either not impregnated or impregnated in very small numbers. Transmission electron microscopy of Alder and Eucalypt woods suggests that ultrastructural differences in the texture and porosity of pit membranes may be the main reason for the observed differences between these wood species with regard to their impregnability by the impregnation material used.


IAWA Journal ◽  
1987 ◽  
Vol 8 (2) ◽  
pp. 134-142 ◽  
Author(s):  
J.R. Barnett

The development of fibre-tracheid pit membranes in Pyrus communis L. has been studied using transmission electron microscopy. Pit fields in the radial walls of cambial cells in transverse section contain isolated plasmodesmata. As cell enlargement proceeds, groups of plasmodesmata develop within thickenings of the future pit membrane. These thickenings are covered by amorphous, secondary-wall-like material (the torus-like structures found in mature pits by Parameswaran ' Liese, 1981) just prior to the end of differentiation and cytoplasmic autolysis. It is suggested that this cap of material acts as aseal, preventing passage of autolytic enzymes from a dying cell to its living neighbour via the perforations occupied by plasmodesmata.


2009 ◽  
Vol 106 (17) ◽  
pp. 7245-7250 ◽  
Author(s):  
Diane M. Martin ◽  
Omid Toub ◽  
Angela Chiang ◽  
Bernard C. Lo ◽  
Sebastian Ohse ◽  
...  

Terpenoid volatiles are important information molecules that enable pollinators to locate flowers and may protect reproductive tissues against pathogens or herbivores. Inflorescences of grapevine (Vitis vinifera L.) are composed of tiny green flowers that produce an abundance of sesquiterpenoid volatiles. We demonstrate that male flower parts of grapevines are responsible for sesquiterpenoid floral scent formation. We describe temporal and spatial patterns of biosynthesis and release of floral volatiles throughout the blooming of V. vinifera L. cv. Cabernet Sauvignon. The biosynthesis of sesquiterpene volatiles, which are emitted with a light-dependent diurnal pattern early in the morning at prebloom and bloom, is localized to anthers and, more specifically, within the developing pollen grains. Valencene synthase (VvValCS) enzyme activity, which produces the major sesquiterpene volatiles of grapevine flowers, is present in anthers. VvValCS transcripts are most abundant in flowers at prebloom stages. Western blot analysis identified VvValCS protein in anthers, and in situ immunolabeling located VvValCS protein in pollen grains during bloom. Histochemical staining, as well as immunolabeling analysis by fluorescent microscopy and transmission electron microscopy, indicated that VvValCS localizes close to lipid bodies within the maturing microspore.


Author(s):  
G. G. Shaw

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.


Author(s):  
R. W. Anderson ◽  
D. L. Senecal

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.


Author(s):  
S. Fujishiro

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.


Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).


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