scholarly journals The in vivo Three-dimensional Form of a Plant Mycoplasma-like Organism by the Analysis of Serial Ultrathin Sections

Microbiology ◽  
1980 ◽  
Vol 116 (1) ◽  
pp. 111-131
Author(s):  
H. Waters ◽  
P. Hunt
1989 ◽  
Vol 93 (2) ◽  
pp. 385-389
Author(s):  
U. KRISTEN ◽  
J. LOCKHAUSEN ◽  
W. MENHARDT ◽  
W. J. DALLAS

Computer-generated three-dimensional reconstructions of higher plant dictyosomes from electron micrographs are presented from different viewing angles in the form of shaded perspective displays. The image processing has revealed complicated structures indicating a central cisternal stack surrounded by a cloud of vesicles and vesicular and tubular protrusions. The entire dictyosome is suggested as being an approximately spherical body that is marginally penetrated by plates and tubules of the endoplasmic reticulum.


Author(s):  
D. Reis ◽  
B. Vian ◽  
J. C. Roland

Wall morphogenesis in higher plants is a problem still open to controversy. Until now the possibility of a transmembrane control and the involvement of microtubules were mostly envisaged. Self-assembly processes have been observed in the case of walls of Chlamydomonas and bacteria. Spontaneous gelling interactions between xanthan and galactomannan from Ceratonia have been analyzed very recently. The present work provides indications that some processes of spontaneous aggregation could occur in higher plants during the formation and expansion of cell wall.Observations were performed on hypocotyl of mung bean (Phaseolus aureus) for which growth characteristics and wall composition have been previously defined.In situ, the walls of actively growing cells (primary walls) show an ordered three-dimensional organization (fig. 1). The wall is typically polylamellate with multifibrillar layers alternately transverse and longitudinal. Between these layers intermediate strata exist in which the orientation of microfibrils progressively rotates. Thus a progressive change in the morphogenetic activity occurs.


Author(s):  
Peter Sterling

The synaptic connections in cat retina that link photoreceptors to ganglion cells have been analyzed quantitatively. Our approach has been to prepare serial, ultrathin sections and photograph en montage at low magnification (˜2000X) in the electron microscope. Six series, 100-300 sections long, have been prepared over the last decade. They derive from different cats but always from the same region of retina, about one degree from the center of the visual axis. The material has been analyzed by reconstructing adjacent neurons in each array and then identifying systematically the synaptic connections between arrays. Most reconstructions were done manually by tracing the outlines of processes in successive sections onto acetate sheets aligned on a cartoonist's jig. The tracings were then digitized, stacked by computer, and printed with the hidden lines removed. The results have provided rather than the usual one-dimensional account of pathways, a three-dimensional account of circuits. From this has emerged insight into the functional architecture.


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