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W A Nicholson

Publications and source records attributed to W A Nicholson.

At least 19 recordsLinked to original sources

The continuum normalization method for quantification of X-ray spectra in biological microanalysis. 1. Generalized bremsstrahlung production cross-sections and analysis using standards.

The thin self-supporting biological specimens used for quantitative X-ray microanalysis are problematical because the sections are most unlikely to be uniform in thickness or density, so the intensities of the characteristic lines alone are not a good measure of composition. The method developed to overcome these problems was introduced by T. A. Hall in 1971 and uses the bremsstrahlung or continuum intensity recorded in the X-ray spectrum to normalize each characteristic line, and hence is frequently referred to as the continuum normalization (CN) procedure. Reformulating the CN method of quantification in terms of generalized cross-sections and calculating more accurate values of bremsstrahlung production using a formula allows us a better understanding of the options open to the analyst of biological thin sections by which the errors in the measurement may be reduced. If one chooses to use the original Hall (1971) method using Kramers cross-sections, the window measuring the continuum for normalization should be set in the 4-7 keV region for typical scanning electron microscope and microprobe beam energies, 20-40 kV, and above 10 keV for transmission electron microscope energies of 80 kV and above. Although it is clear that peak counts must not contribute to the white count, the window should be as wide as possible to reduce statistical errors.

Journal Article↗

Standardless analysis of biological tissue sections.

The X-ray microanalysis of thin biological samples which are usually supported on a thin organic film or are self-supporting specimens, has required the use of standards which contain the elements of interest. Spectra from the standards are used to calculate the factors for converting X-ray data recorded on the specimen into elemental concentrations. A method is discussed here, in which these factors are evaluated from formulae. The most important physical process to be evaluated is that of characteristic X-ray production in the specimen. The bremsstrahlung production must also be evaluated if the Hall or continuum normalisation (CN) method of quantitation is to be used. This paper discusses briefly methods of calculating values for the X-ray production cross-sections for both characteristic and bremsstrahlung radiation. The way in which these are incorporated into standardless quantitation methods for biological samples is described. Calculations of some cross-section data are presented for typical analytical conditions.

Animals↗

Preparation of cryosections with a modified Sorvall MT2B ultramicrotome and cryoattachment.

The Sorvall MT2B ultramicrotome and cryoattachment were modified to extent the duration of cutting and to overcome problems in tissue preparation. Microtome and cryochamber were encased and surrounded by an atmosphere of dry nitrogen gas at room temperature. A specially designed cold block sited within the box close to the microtome enabled tissues to be trimmed at low temperatures in the dry environment. Tissues could be readily visualized both on the trimming block and in the chamber with the existing microscope modified to improve its working distance and lighting system. During transfer from storage in liquid nitrogen, through the trimming procedure, to arrival in the cryochamber, the temperature of tissues as determined using thermocouples embedded in PVP on a stub, never exceeded 140 K. Although there was a considerable standing temperature gradient within the cryochamber, the cutting environment, specimen and edge of the knife were thermally stable. Sections could be routinely cut dry and freeze-dried within the chamber, if desired.

Animals↗

A low x-ray background low temperature specimen stage for biological microanalysis in the TEM.

The side entry specimen stage described in this paper is a development of a specimen stage for use at room temperature in the JEOL JEM 100 and 200 series transmission electron microscopes. The earlier specimen stage was designed to ensure that the extraneous instrumental contribution to thin specimen X-ray spectra is both small and quantifiable. As well as having a low X-ray background the new stage will also maintain the specimen at temperatures sufficiently low (down to 100 K) to minimize the loss of organic material due to electron irradiation. A new anticontaminator which provides a clean low temperature environment for the specimen stage is also described.

Cold Temperature↗

Quantitation and localisation of aluminum in human cancellous bone in renal osteodystrophy.

There is increasing evidence that aluminium toxicity may be responsible for a type of vitamin D-resistant osteomalacia and an unusually severe form of dementia ("dialysis dementia") occurring in some patients with chronic renal failure on regular haemodialysis. High concentrations of Al have been found in blood, bone and brain tissue from these patients. The A1 comes either from the water used during dialysis (added in some public water supplies during purification to precipitate contaminants) or from aluminium salts taken orally to bind phosphates and so restrict their dietary adsorption. Recent X-ray microanalytical studies have demonstrated Al in lysosomes of cerebral cells and at the calcification front in bone of patients dying of dialysis dementia but its concentration at this site in bone has not been measured using this technique. We have examined transiliac bone biopsies from 3 patients with dialysis dementia and 6 non-demented patients on regular haemodialysis, Atomic absorption spectrometry (AAS) reveals high Al content in bone from the 3 demented and 2 of the non-demented patients. All had vitamin D-resistant osteomalacia. Using X-ray microanalysis Al was located in the bone of these five patients only. The Al had a highly focal distribution and was measured at up to 40 times higher concentration than by AAS but only in mineralisation nuclei of the calcification front or less than 2 micrometer into the mineralized bone. The study was done retrospectively on biopsies fixed in 10% buffered formalin, which almost certainly eluted some of the Al. In life, Al levels may have been higher than those we have detected.

Adolescent↗

Aspects of microprobe analysis of mineralized tissues.

Mineralizing tissues were the first biological specimens to be examined by the electron microprobe. The necessity for performing analyses at high spatial resolution has led to the increasing use of energy dispersive (ED) detectors in CTEMs/STEMs. Because the ED detector accepts x-rays from a large solid angle, it often detects a large extraneous x-ray contribution from the instrument. By carefully redesigning and remaking the specimen stage and its environment from aluminium, the instrumental contribution may be subtracted from spectra recorded on this specimens. Measurements of the apparent concentrations of Ca and P in araldite due to extraneous x-rays from other parts of the specimen, show that accurate quantitative analyses of Ca and P may be performed in unmineralized organic matrix such as osteoid, despite the proximity of fully mineralized tissue. Quantitative microprobe analyses have been performed on 1) intracellular mineral deposits, 2) osteoid, 3) mineralized matrix in trabecular bone from rachitic (R), vitamin D-treated (D) and normal (N) rats. The composition of the intracellular mineral deposits was similar in all 3 groups with mean Ca:P molar ratios = approximately 1.0. The Ca and P levels in osteoid from each group were sufficiently high that, assuming: a) that all of the Ca and P was in ionized form and b) that osteoid has a water content of 59% the calculated [Ca2+] x [HPO4(2-)] products were much greater than that required for spontaneous precipitation of mineral. In the D and N groups, the Ca and P concentrations in mineralized matrix increased with increasing distance into bone, but in the R group they remained constant. The Ca:P molar ratios of the mineralized matrix and of the serum were highest in the R group (bone: 1.85--1.87, serum: 5.76 +/- 1.05), intermediate in the D group (bone: 1.72--1.90, serum: 2.46 +/- 0.36) and lowest in the N group (bone: 1.68--1.80, serum: 1.25 +/- 0.17).

Bone Matrix↗

Comparison of the methods of cathodoluminescence, electronprobe microanalysis, and calcium staining, applied to human aorta with isthmus stenosis.

Electron probe x-ray microanalysis is a useful method for studying pathologic and age-related calcification mechanisms in the aorta and in muscular arteries by means of elemental analysis in microareas. In the present investigation, this method was correlated with the histochemical alizarin-S-calcium staining and with cathodoluminescence analysis in the scanning electron microscope. Portions of the proximal region of a human aorta with isthmus stenosis was shock-frozen and sectioned in a cryostat. Serial sections were investigated by calcium staining, electron probe, and cathodoluminescence microanalysis. Using quantitative electron probe microanalysis of calcium and phosphorus, it was shown that the principal regions of calcium phosphate mineralization could be located using either alizarin-S staining or cathodoluminescence analysis. The advantage of the cathodoluminescence analysis is its higher lateral resolution compared with that of light microscopy, and the fact that no special staining is required. In addition, it was possible to obtain scanning images, thus providing additional information about the topology of the tissue surface, which is necessary to decide whether or not the section is suitable for microanalysis. Quantitative microanalysis is a valuable tool for basic research on calcified arteries. The results of the combined analysis in the proximal and distal regions as well as in the stenosis will be published in a later paper.

Aortic Coarctation↗

Electron microprobe investigations into the process of hard tissue formation.

The electron microprobe microanalyser has been used to measure the concentrations of Ca, P and S in the predentine of young rat incisors. The specimens were prepared as alcohol embedded ultrathin sections, unfixed vacuum embedded dry cut ultrathin sections and as thin cryostat sections. The results show the influence of preparation on the measured compositions and indicate that Ca is tightly bound to the matrix, whereas P can be easily washed out. Measurements along the dentine-predentine border demonstrated zones of Ca enrichment, the average size of which suggests that the zones could be the prestages of calcospherites. A mineralisation mechanism is discussed in which the high Ca concentration activates pyrophosphosphatase or ATPase before the onset of nucleation.

Animals↗

Changing sex ratios in diabetes.

A survey of sexes and ages in patients attending the Hartlepool diabetic clinic was carried out for the 20-year period 1948-67. The proportion of men aged 50 and over rose from 25.9% in the first decade to 38.2% in the second. An attempt has been made to explain this pronounced and rapid change.

Adolescent↗