𝔖 Bobbio Scriptorium
✦   LIBER   ✦

High resolution and image processing of otoconia matrix

✍ Scribed by C. D. Fermin


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
913 KB
Volume
25
Category
Article
ISSN
1059-910X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

This study was designed to investigate patterns of fibrils organization in histochemically stained otoconia. Transmission electron microscope and video imaging were used. These data indicate that otoconia of the chick (Gallus domesticus) inner ear may have central cores in vivo. The data also show that the ultrastructural organization of fibrils fixed with aldehydes and histochemical stains follows trajectories that conform to the hexagonal shape of otoconia. These changes in direction may contribute to the formation of a central core. The existence of central cores is important for the in vivo buoyancy of otoconia. Packing of fibrils is tighter after phosphotungstic acid (PTA) stained otoconia than with other histochemical stains, which usually produce looser packing of fibrils and seemingly larger central core. TEM of tilted and untilted material showed that turning of fibrils occurs at the points where the face angles of otoconia form and where central cores exist. Video image processing of the images allowed reconstructing a template which, if assumed to repeat and change trajectories, would fit the pattern of fibrils seen in fixed otoconia. Since it is highly unlikely that aldehyde primary fixation or PTA stain caused such drastic change in the direction of fibrils, the template derived from these results may closely approximate patterns of otoconia fibrils packing in vivo. However, if the above is correct, the perfect crystallographic diffraction pattern of unfixed otoconia do not correspond to patterns of fixed fibrils. Β© 1993 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Image processing based on the combinatio
✍ Li, F.H. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 743 KB

A method of crystal structure determination by electron crystallographic image processing based on the combination of high-resolution electron microscopy (HREM) and electron diffraction is introduced. It consists of two stages: image deconvolution and resolution enhancement. In the first stage an i

Matrix-free high-resolution imaging mass
✍ Yoshihiko Nakata; Yoshiro Honda; Satoshi Ninomiya; Toshio Seki; Takaaki Aoki; Ji πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 312 KB

## Abstract The importance of imaging mass spectrometry (MS) for visualizing the spatial distribution of molecular species in biological tissues and cells is growing. We have developed a new system for imaging MS using MeV ion beams, termed MeV‐secondary ion mass spectrometry (MeV‐SIMS) here, and d