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The Microscope – Volume 62, Third Quarter 2014

IN THIS ISSUE
On the cover
A cross section of a pixie chocolate candy captured with an NSI Imagix X-ray Tomography System, showing chocolate (light gray), caramel (white) and pecan (dark gray). See Inter/Micro 2014 abstract, Three-Dimensional Visualization Using X-ray Tomography, page 105. (Photo courtesy of Robert G. Myers and Philip W. Urnezis)
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Editorial | In Light Microscopy, It’s a ‘Nanoworld’ After All
Gary J. LaughlinThe Microscope 62:3, p. ii, 2014https://doi.org/10.59082/WYWT1071 Excerpt: It is not very often that microscopy, let alone light microscopy, makes front-page news — but it did recently. I would like to extend our congratulations and thanks to the 2014 Nobel Prize laureates in chemistry: Eric Betzig, Stefan Hell and William Moerner for the “development of super-resolved fluorescence microscopy.”
Inter/Micro 2014
Gary J. Laughlin The Microscope 62:3, pp. 99–115, 2014https://doi.org/10.59082/DXTW5214
Abstract: McCrone Research Institute held the 66th annual Inter/Micro microscopy conference on June 2–6 in its lecture rooms and laboratories in Chicago, drawing attendees from around the world. Participants heard indepth research presentations by leading microscopists, who covered advancements in instrumentation, techniques and applications in various fields of microscopy and microanalysis. Presentations focused on PLM, SEM, EDS, Raman, hot stage and infrared microspectroscopy; microchemistry; forensic trace evidence and criminalistics; pharmaceutical sciences; materials analysis; environmental health; food analysis; and air quality.
Microhistology of Plant Material Using Low-Cost Materials for Polarized Light Microscopy
John J. Henderson, Gary Phillips and Joseph T. SpringerThe Microscope 62:3, pp. 117–121, 2014 https://doi.org/10.59082/JCBO5735 Abstract: Microhistology is the term commonly given to the microscopic study of animal feces. A microscopic study of feces is completed to determine the diet of carnivores or herbivores and to observe parasites that have passed the digestive system. Cellular fragments, such as cellular structures (stomata, cells, tracheae, etc.) and epidermal surface attachments (trichomes, scales, glands, etc.), are commonly viewed with traditional brightfield microscopy. Crystal and non-crystal inclusions (silica, calcium compounds, starch, etc.), along with some biological materials (starch, tracheids, etc.) are enhanced with the use of polarized light. However, polarized light microscopy (PLM) is seldom used in biological laboratories. Luckily, simple and inexpensive attachments can be used for basic polarized light to enhance microhistological fragments for better identification.
Critical Focus | Crisis Point: The Rise and Fall of Penicillin
Brian J. FordThe Microscope 62:3, pp. 123–135, 2014 https://doi.org/10.59082/TZES5386 Excerpt: Our lives are at risk. The World Health Organization (WHO) says there is a global security threat that requires action across government sectors and society as a whole. In Atlanta, the Centers for Disease Control and Prevention (CDC) are similarly blunt, describing the situation as a nightmare. In London, Chief Medical Officer Sally Davies, says we now face a catastrophic threat. What is it? International terrorism? No, says Davies, the danger is greater than terrorism.
The Microscope Past: 40 Years Ago | Common Errors in Subnanogram Particle X-ray Analysis
J. Gavrilovic The Microscope 62:3, pp. 137–140, 2014Originally published in The Microscope, Vol. 22, Third Quarter, 1974. Introduction: Chemical composition of subnanogram particles (<10 μm) can be readily attained by a number or techniques such as electron microprobe X-ray analysis, ion microprobe mass analysis or, less readily, even laser microprobe spectral analysis. The most widely used technique, however, is X-ray analysis as employed in all electron microprobes and most scanning microscopes. Both of these instruments utilize electron excited X-rays for identification of the elements in a small particle. With high-resolution semi-conductor type energy dispersive spectrometers, a complete semi-quantitative analysis of a one micrometer particle can be carried out within 10 seconds. A fully quantitative analysis of a small particle obviously takes more time, but produces more reliable quantitative information about the chemical composition of a small particle than any other ultramicrotechnique (subnanogram samples). Because of the widespread use of X-ray techniques for chemical identification of small particles, it is important to recognize the nature and magnitude of possible errors in such an analysis.
Afterimage | Man-Made Wig Fibers
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Theresa Joslin and Patrick Buzzini — Forensic and Investigative Science Department, West Virginia University, Morgantown, WV The Microscope 62:3, p. 144, 2014 Cross-sectional shapes of modacrylic wig fibers. This brown wig is composed of four different types of fibers: 1) light-brown horseshoe shape, 2) dark-brown horseshoe shape, 3) orange dogbone shape, and 4) orange hexalobular shape. Cross-sections were prepared using the Joliff method. (Photo courtesy of Patrick Buzzini)
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