scholarly journals Studies of the Fine Structure of the Wax Layer of Sultana Grapes

1963 ◽  
Vol 16 (4) ◽  
pp. 818 ◽  
Author(s):  
TC Chambers ◽  
JV Possingham
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Drying Rate ◽  
Distilled Water ◽  
Replica Technique ◽  
Carbon Replica

The surface waxy bloom of sultana grapes has been studied using the carbon. replica technique in combination with electron microscopy. This layer consists of a series of overlapping wax platelets, each of which is about 0�1 f' wide. The air spaces between the wax platelets become filled with liquid when sultana berries are dipped in commercial emulsions known to accelerate their drying rate. Washing in distilled water removes this layer of dipping emulsion from the surface. The appearance of dipped and washed grapes is similar to that of untreated grapes.

scholarly journals Cuticular Transpiration and Wax Structure and Composition of Leaves and Fruit of Vitis Vinifera

1967 ◽  
Vol 20 (6) ◽  
pp. 1149 ◽  
Author(s):  
JV Possingham ◽  
TC Chambers ◽  
F Radler ◽  
M Grncarevic
Keyword(s):  
Fine Structure ◽  
Chemical Composition ◽  
Vitis Vinifera ◽  
Light Petroleum ◽  
Replica Technique ◽  
Carbon Replica ◽  
Cuticular Transpiration ◽  
Leaf Wax ◽  
Surface Wax ◽  
Platelet Structure

The fine structure of the surface wax of leaves of sultana vines (Vitia viiUJera var. sultana) has been examined using the carbon replica technique. Leaf wax was found to be morphologically similar to the wax on the surface of grapes and to consist of a series of overlapping platelets. A brief period (30 sec) of exposure to light petroleum vapour disorganized the platelet structure of both leaf and fruit wax. This treatment markedly increased the cuticular transpiration of both fruits and leaves. The results are discussed in relation to the known chemical composition of these waxes. It is suggested that the surface wax, which consists of overlapping platelets that are hydrophobic in nature, may be important in controlling cuticular transpiration in both the fruit and leaves of grape.vines.

scholarly journals The Structure of the Cuticular Wax of Prune Plums and its Influence as a Water Barrier

1967 ◽  
Vol 20 (5) ◽  
pp. 895 ◽  
Author(s):  
Joan M Bain ◽  
D Mcg Mcbean
Keyword(s):  
Electron Microscopy ◽  
Outer Layer ◽  
Layer Structure ◽  
Cuticular Wax ◽  
Replica Technique ◽  
Carbon Replica ◽  
Water Barrier

Wax on the surface of prune plums, sampled from 2 weeks before fruit was mature until 2 weeks after, was shown by electron microscopy, using the carbon� replica technique, to occur in a two-layer structure. The iruier layer consisted of a matrix of thin platelets, while the outer layer was composed of fragile projections, many of which appeared tubular. The incidence and complexity of the projections in the outer layer increased as the fruit matured.

Fine Structure of Pollen Grain Ektexine of Maize, Teosinte and Tripsacum

1972 ◽  
Vol 30 ◽  
pp. 226-227
Author(s):  
Umesh C. Banerjee ◽  
Elso S. Barghoorn
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Zea Mays ◽  
Fine Structure ◽  
Light Microscope ◽  
Pollen Grains ◽  
Pollen Grain ◽  
Wild Relatives ◽  
Distilled Water ◽  
Scanning Electron

Using light microscope (LM) it was found very difficult to distinguish the ektexine (outer sculptured layer of exine) pattern of maize (Zea mays L.) pollen grains from that of its wild relatives teosinte (Euchlaena mexicana Schrad.) and tripsacum (Tripsacum spp.). At the magnifications obtained by LM, the pollen grain ektexine is faintly granular or netted. By the use of electron microscopy, however, it is possible to characterize their pollen ektexine patterns.For scanning electron microscopy (SEM) acetolysed pollen grains were used. After acetolysis the pollen samples were washed several times in glass-distilled water to remove traces of acids. Each sample was dispersed in a drop of distilled water placed on specimen holders.

Fine structure of normal and regenerated shell of Helix

1971 ◽  
Vol 49 (1) ◽  
pp. 37-41 ◽  
Author(s):  
A. S. M. Saleuddin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fine Structure ◽  
Organic Matrix ◽  
Nacreous Layer ◽  
Replica Technique ◽  
Thin Sections ◽  
Thin Sectioning ◽  
Inorganic Components ◽  
Scanning Electron

Fine structure of the normal and the regenerated shell of Helix has been studied by thin sectioning, replica technique, and scanning electron microscopy. Normal shell consists of four calcareous layers: innermost nacreous, two cross lamellar, and outermost prismatic. Crystals of the shell are well defined and are surrounded by intercrystalline organic matrix. Intracrystalline organic matrix is recognized, particularly in decalcified sections. Interrelationships between the organic and inorganic components have been studied in decalcified thin sections. Regenerated shell appears similar to nacreous layer of the normal shell. Crystals are large and stacked like bricks. Intracrystalline organic matrix is very prominent. Electron diffraction of the crystals of the regenerated shell generally gives calcite pattern whereas the normal shell gives aragonite. Surface topography of the normal and regenerated shell has been compared by replica techniques.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

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).

Surface Structure of Nucleated Animal Cells: Carbon Replicas

1967 ◽  
Vol 25 ◽  
pp. 120-121
Author(s):  
Robert M. Glaeser ◽  
Thea B. Scott
Keyword(s):  
Cell Surface ◽  
Surface Structure ◽  
Particle Diameter ◽  
Cellular Functions ◽  
Animal Cells ◽  
Replica Technique ◽  
Carbon Replica ◽  
Characteristic Particle ◽  
Cell Surface Structure ◽  
Carbon Replicas

The carbon-replica technique can be used to obtain information about cell-surface structure that cannot ordinarily be obtained by thin-section techniques. Mammalian erythrocytes have been studied by the replica technique and they appear to be characterized by a pebbly or “plaqued“ surface texture. The characteristic “particle” diameter is about 200 Å to 400 Å. We have now extended our observations on cell-surface structure to chicken and frog erythrocytes, which possess a broad range of cellular functions, and to normal rat lymphocytes and mouse ascites tumor cells, which are capable of cell division. In these experiments fresh cells were washed in Eagle's Minimum Essential Medium Salt Solution (for suspension cultures) and one volume of a 10% cell suspension was added to one volume of 2% OsO4 or 5% gluteraldehyde in 0.067 M phosphate buffer, pH 7.3. Carbon replicas were obtained by a technique similar to that employed by Glaeser et al. Figure 1 shows an electron micrograph of a carbon replica made from a chicken erythrocyte, and Figure 2 shows an enlarged portion of the same cell.

Fibroblasts During Hypertrophic Scar Formation and Resolution

1973 ◽  
Vol 31 ◽  
pp. 428-429
Author(s):  
C. W. Kischer
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Cell Proliferation ◽  
Fine Structure ◽  
Metabolic Activity ◽  
Hypertrophic Scar ◽  
Normal Skin ◽  
Ground Substance ◽  
Hypertrophic Scars ◽  
Scanning Electron

The morphology of the fibroblasts changes markedly as the healing period from burn wounds progresses, through development of the hypertrophic scar, to resolution of the scar by a self-limiting process of maturation or therapeutic resolution. In addition, hypertrophic scars contain an increased cell proliferation largely made up of fibroblasts. This tremendous population of fibroblasts seems congruous with the abundance of collagen and ground substance. The fine structure of these cells should reflect some aspects of the metabolic activity necessary for production of the scar, and might presage the stage of maturation.A comparison of the fine structure of the fibroblasts from normal skin, different scar types, and granulation tissue has been made by transmission (TEM) and scanning electron microscopy (SEM).

Variations in Surface Textures of Quartz Sand using Electron Microscopy

1970 ◽  
Vol 28 ◽  
pp. 494-495
Author(s):  
Eugene J. Amaral
Keyword(s):  
Electron Microscopy ◽  
Glass Industry ◽  
Glass Slide ◽  
Distilled Water ◽  
Early Paleozoic ◽  
Secondary Effects ◽  
Surface Textures ◽  
High Silica ◽  
Sand Deposit ◽  
The U.S

Examination of sand grain surfaces from early Paleozoic sandstones by electron microscopy reveals a variety of secondary effects caused by rock-forming processes after final deposition of the sand. Detailed studies were conducted on both coarse (≥0.71mm) and fine (=0.25mm) fractions of St. Peter Sandstone, a widespread sand deposit underlying much of the U.S. Central Interior and used in the glass industry because of its remarkably high silica purity.The very friable sandstone was disaggregated and sieved to obtain the two size fractions, and then cleaned by boiling in HCl to remove any iron impurities and rinsed in distilled water. The sand grains were then partially embedded by sprinkling them onto a glass slide coated with a thin tacky layer of latex. Direct platinum shadowed carbon replicas were made of the exposed sand grain surfaces, and were separated by dissolution of the silica in HF acid.

Studies of Circular DNA Using a New Electron Microscopic Technique

1973 ◽  
Vol 31 ◽  
pp. 596-597
Author(s):  
C. N. Gordon
Keyword(s):  
Electron Microscopy ◽  
Aqueous Salt Solution ◽  
Contour Length ◽  
Cleavage Surface ◽  
Mica Substrate ◽  
Electron Microscopic ◽  
Replica Technique ◽  
Circular Dna ◽  
Transmission Electron ◽  
Electron Microscopic Technique

Gordon and Kleinschmidt have described a new preparative technique for visualizing DNA by electron microscopy. This procedure, which is a modification of Hall's “mica substrate technique”, consists of the following steps: (a) K+ ions on the cleavage surface of native mica are exchanged for Al3+ ions by ion exchange. (b) The mica, with Al3+ in the exchange sites on the surface, is placed in a dilute aqueous salt solution of DNA for several minutes; during this period DNA becomes adsorbed on the surface. (c) The mica with adsorbed DNA is removed from the DNA solution, rinsed, dried and visualized for transmission electron microscopy by Hall's platinum pre-shadow replica technique.In previous studies of circular DNA by this technique, most of the molecules seen were either broken to linears or extensively tangled; in general, it was not possible to obtain suitably large samples of open extended molecules for contour length measurements.

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