Abstract

X-ray microanalysis and scanning electron microscopy used in conjunction with cold-stage techniques to examine frozen-hydrated bulk biological tissue is a promising method to determine the concentration and distribution of diffusible elements which are typically distorted by conventional techniques of biological tissue fixation. The proper application of this method, however, requires an understanding of the freezing and sublimation processes in bulk biological specimens, and the interaction of the electron beam with the bulk specimen in the frozen-hydrated state. These factors have been evaluated and are discussed below.One of the fundamental considerations in the examination of cryofixed bulk tissue is the formation of exogenous and endogenous ice crystals within the specimen or upon the surface of the specimen which can lead to tissue distortion and ion translocation. Techniques to minimize the exposure of the specimen to atmospheric conditions and to eleminate the formation of exogenous ice crystals have been developed by Burgio et al. (1978a), and Echlin and Moreton (1974).

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