Somitogenesis in the amphibian Xenopus laevis: scanning electron microscopic analysis of intrasomitic cellular arrangements during somite rotation

Development ◽  
1981 ◽  
Vol 64 (1) ◽  
pp. 23-43
Author(s):  
B. Woo Youn ◽  
George M. Malacinski

The intrasomitic changes in cell arrangement which accompany somite rotation during somitogenesis in Xenopus laevis were analysed with the scanning electron microscope (SEM). Longitudinal, horizontal fractures of whole embryos were examined at various dorsoventral levels of stage-22 to -24 embryos. Observations of the gross morphological features of somitogenesis, and the cellular changes which accompany somite segmentation and somite rotation were made. Several of these observations lead to modifications of previous models for the cellular basis of somitogenesis in Xenopus. Individual cellular rearrangements, rather than simultaneous block rotation of a whole somite, appear to be responsible for the 90° rotation of myotomal cells within a single somite. Cellular arrangments in fused somites were also examined. Some ultraviolet-irradiated embryos displayed a complete lack of a notochord. The somites in those embryos were fused across the midline beneath the neural tube. The dorsal and ventral arms of the somites are not fused. Normal rotation occurs only in the dorsal and ventral arms while, in the majority of cases, cells in the fused region fail to rotate normally. In some cases, individual cells in the fused region undergo partial rearrangement. Those observations support the notion that individual cellular rearrangements account for the rotation of the whole somite.

Author(s):  
M.D. Graham

The recent development of the scanning electron microscope has added great impetus to the study of ultrastructural details of normal human ossicles. A thorough description of the ultrastructure of the human ossicles is required in order to determine changes associated with disease processes following medical or surgical treatment.Human stapes crura were obtained at the time of surgery for clinical otosclerosis and from human cadaver material. The specimens to be examined by the scanning electron microscope were fixed immediately in the operating room in a cold phosphate buffered 2% gluteraldehyde solution, washed with Ringers, post fixed in cold 1% osmic acid and dehydrated in graded alcohol. Specimens were transferred from alcohol to a series of increasing concentrations of ethyl alcohol and amyl acetate. The tissue was then critical point dried, secured to aluminum stubs and coated with gold, approximately 150A thick on a rotating stage in a vacuum evaporator. The specimens were then studied with the Kent-Cambridge S4-10 Scanning Electron Microscope at an accelerating voltage of 20KV.


1999 ◽  
Vol 5 (S2) ◽  
pp. 328-329
Author(s):  
M. Amy Sheldon

Research into bone histology of fossil material is a growing area of inquiry in vertebrate paleontology. Incorporating histological study into ontogenetic investigation presents new opportunities for gaining data to better understand ontogeny, ecology, and evolution of mosasaurs. Adding scanning electron microscopy to the growing technology being applied to fossil research can only further the understanding of long extinct animals.Mosasaurs were totally marine lizards which inhabited both open ocean and epicontinental seas during the late Cretaceous (Turonian through Maestrichtian), approximately 90-65. million years ago. Mosasaurs have been collected from many areas of North America. The specimens used in this study were collected from Alabama, Kansas, South Dakota, and Texas. I have restricted the fossil material for destructive analysis to ribs and vertebrae. Ribs have not been shown to have importance in morphological analysis relating to systematics or evolution, therefore their destruction does not imped the research of others. Vertebrae were isolated on outcrop but could be identified to genus and growth stage.


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