Fine structure of teliospores of the cedar-apple rust Gymnosporangium juniperi-virginianae

1975 ◽  
Vol 53 (6) ◽  
pp. 544-552 ◽  
Author(s):  
Charles W. Mims ◽  
Frank Seabury ◽  
E. L. Thurston
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Basal Cell ◽  
Spore Wall ◽  
Cellular Structures ◽  
Lipid Bodies ◽  
Germ Pore ◽  
Transmission Electron ◽  
Single Nucleus

Teliospores of the cedar-apple rust Gymnosporangium juniperi-virginianae were examined using transmission electron microscopy. Each ellipsoid spore is divided into two cells by a transverse septum. A second septum separates the basal cell of the teliospore from a long, hyaline, cylindrical pedicel. The fine structure of these septa is considered. The cytoplasm of the teliospore is very dense and contains a complement of cellular structures including ribosomes, vacuoles, mitochondria, and a large number of structures thought to be lipid bodies. Each cell of the teliospore contains a single nucleus, in which the chromatin is often considerably condensed. Two germ pore regions are present in each cell. The spore wall is thinnest in these regions and is different in structure than elsewhere around the spore.

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).

Fine structure and possible functions of the hermaphrodite duct of some pulmonate snails (Mollusca: Gastropoda)

1990 ◽  
Vol 48 (3) ◽  
pp. 68-69
Author(s):  
Alan N. Hodgson
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Seminal Vesicle ◽  
Reproductive Biology ◽  
Light Microscope ◽  
Light Microscope Level ◽  
Transmission Electron ◽  
Standard Techniques

The hermaphrodite duct of pulmonate snails connects the ovotestis to the fertilization pouch. The duct is typically divided into three zones; aproximal duct which leaves the ovotestis, the middle duct (seminal vesicle) and the distal ovotestis duct. The seminal vesicle forms the major portion of the duct and is thought to store sperm prior to copulation. In addition the duct may also play a role in sperm maturation and degredation. Although the structure of the seminal vesicle has been described for a number of snails at the light microscope level there appear to be only two descriptions of the ultrastructure of this tissue. Clearly if the role of the hermaphrodite duct in the reproductive biology of pulmonatesis to be understood, knowledge of its fine structure is required.Hermaphrodite ducts, both containing and lacking sperm, of species of the terrestrial pulmonate genera Sphincterochila, Levantina, and Helix and the marine pulmonate genus Siphonaria were prepared for transmission electron microscopy by standard techniques.

Direct Observation of Fine Structure within Images of Atoms in Crystals by Transmission Electron Microscopy

1977 ◽  
Vol 42 (3) ◽  
pp. 1073-1074 ◽  
Author(s):  
Hatsujiro Hashimoto ◽  
Hisamitsu Endoh ◽  
Takayoshi Tanji ◽  
Akishige Ono ◽  
Eiichi Watanabe
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Direct Observation ◽  
Transmission Electron

Ultrastructural morphology of the uredium and collar formation during urediosporogenesis of Uromyces transversalis on gladiolus

1990 ◽  
Vol 68 (3) ◽  
pp. 605-612 ◽  
Author(s):  
Johan F. Ferreira ◽  
F. H. J. Rijkenberg
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Basal Cell ◽  
Basal Layer ◽  
Ultrastructural Morphology ◽  
Transmission Electron

The transverse uredia of Uromyces transversalis on gladiolus leaves were investigated by scanning and transmission electron microscopy. The basal cell forms one or more protuberances distally, each being delimited by a septum to become a urediospore initial. The initial elongates and lays down a septum to form a urediospore and pedicel. The first protuberance on the basal cell forms holoblastically, and evidence is found at the same locus for the subsequent enteroblastic formation of up to three successive urediospore initials. The pedicel wall of a spore thus formed remains on the basal cell and becomes a collar around the next protuberance. The basal layer of the two-layered septum that delimited the pedicel from the basal cell grows out to form the wall of the subsequent protuberance, and in the process ruptures and laterally displaces the terminal septal layer. A new basipetal septum forms to delimit the subsequent urediospore initial. In this manner, several collars form retrogressively and concentrically at one locus.

Parental Stress and Prechilling Effects on Pennsylvania Smartweed (Polygonum pensylvanicum) Achenes

Weed Science ◽  
1982 ◽  
Vol 30 (3) ◽  
pp. 243-248 ◽  
Author(s):  
James L. Jordan ◽  
David W. Staniforth ◽  
Catalina M. Jordan
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Zea Mays ◽  
Parental Stress ◽  
Cell Walls ◽  
Lipid Bodies ◽  
Transmission Electron ◽  
Polygonum Pensylvanicum ◽  
Scanning Electron

Pennsylvania smartweed (Polygonum pensylvanicum L.) achenes were harvested from plants growing either free from competition or in competition with corn (Zea mays L. ‘Pioneer 3780′) plants. Seeds were dormant when harvested. After 15 weeks of prechilling, 4 and 35% of the seeds germinated from plants with and without corn competition, respectively; after 30 weeks of prechilling, more than 92% of all seeds germinated. Scanning electron microscopy revealed that the carpel walls of achenes from plants with corn competition were porous with many channels. Carpel walls of achenes from plants without corn competition were without pores and channels. Transmission electron microscopy showed more lipid bodies in the embryo epidermal cells of seeds from plants with corn competition. Cell walls of embryos from non-prechilled seeds from plants with corn competition contained lipoidosomes that traversed cell walls. Lipoidosomes did not occur in cells of prechilled seeds.

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