Toward a Comprehensive Upper Quaternary Tephra and Ignimbrite Stratigraphy in New Zealand using Electron Microprobe Analysis of Glass Shards

1983 ◽  
Vol 19 (2) ◽  
pp. 188-200 ◽  
Author(s):  
P. C. Froggatt

AbstractNew Zealand Quaternary marine and terrestrial sequences contain numerous tephras, or volcanic-ash horizons, that are the distal correlatives of voluminous welded ignimbrite sheets, erupted from central North Island. Electron microprobe analyses of glass shards from the distal tephras demonstrate their homogeneity and are shown to identify each tephra examined. By matching tephras from stratigraphically controlled sequences, the first comprehensive tephra stratigraphy spanning from 50,000 to 700,000 yr ago and covering the New Zealand region is advanced.Analyses on glass shards from the unwelded base of ignimbrite sheets are comparable to the distal tephra analyses and allow correlation between ignimbrites and to the distal tephras. The better exposed tephra record constrains the number of separate eruptive events and the stratigraphy of the ignimbrites, both of which were previously confused by lack of outcrop.Samples from pumiceous marine sediments were found to contain two or more chemically distinct populations of glass. The pumice is in cross-bedded sands or sand lenses within conglomerate, attesting to a shallow high-energy environment where reworking could occur. However, each glass population could be matched to older, known tephras.

Author(s):  
R. I. Johnsson-Hegyeli ◽  
A. F. Hegyeli ◽  
D. K. Landstrom ◽  
W. C. Lane

Last year we reported on the use of reflected light interference microscopy (RLIM) for the direct color photography of the surfaces of living normal and malignant cell cultures without the use of replicas, fixatives, or stains. The surface topography of living cells was found to follow underlying cellular structures such as nuceloli, nuclear membranes, and cytoplasmic organelles, making possible the study of their three-dimensional relationships in time. The technique makes possible the direct examination of cells grown on opaque as well as transparent surfaces. The successful in situ electron microprobe analysis of the elemental composition and distribution within single tissue culture cells was also reported.This paper deals with the parallel and combined use of scanning electron microscopy (SEM) and the two previous techniques in a study of living and fixed cancer cells. All three studies can be carried out consecutively on the same experimental specimens without disturbing the cells or their structural relationships to each other and the surface on which they are grown. KB carcinoma cells were grown on glass coverslips in closed Leighto tubes as previously described. The cultures were photographed alive by means of RLIM, then fixed with a fixative modified from Sabatini, et al (1963).


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