In the field of document examination, several approaches can be taken to probe the authenticity of a piece of ancient writing. Scholars have the task of analyzing, and possibly translating, the language and content of a document, and assessing the character and quality of the script. Materials characterization plays another role. Both the document substrate and the ink can be examined to determine whether the materials and methods of creation are consistent with those known to be used during the historical period to which the document is attributed.

Electron microscopy and x-ray microanalysis are common techniques in many research, development and quality labs (Garratt-Reed and Bell, 2002; Goldstein et al., 2003). As systems become ever more automated, as well as easy to use, new applications for the use of these systems develop and expand. One such application is particle analysis. These “particles” might be small loose fragments that can be applied to a conductive adhesive or a filter, embedded in epoxy and polished, or they can be inclusions within collect an EDS spectrum.

A silicon multi-cathode detector (SMCD) has been developed for microanalysis and x-ray mapping applications. The SMCD has a large active area (∼0.5 cm2), excellent energy resolution, and high count rate capability. The detector utilizes novel structures that have produced very low dark current, high electric field, uniform charge collection, low noise and high sensitivity to low energy x-rays. The detector's spectral response was evaluated using a 55Fe radioisotope source, as well as by fluorescing materials with an x-ray generator. Figure 1 shows a 55Fe spectrum with an energy resolution of 125 eV FWHM at 5.9 keV collected at 12 μs peaking time. This energy resolution has been repeatably measured on many different detectors. To evaluate the high count rate x-ray performance, which is very important for fast x-ray mapping, a Cu sample was fluoresced using a Rh-anode x-ray tube.

Fluctuation microscopy is the enigmatic name given to an otherwise straightforward technique for studying medium range order in highly disordered materials. By medium range, we mean atomic ordering at length scales within the range 0.5-2.0 nm, where traditional imaging and diffraction techniques have the most difficulty detecting structural correlations in amorphous materials. Puzzlement over fluctuation microscopy generally arises not because of the "microscopy" part of the name, but because of the "fluctuation" part. What, exactly, is fluctuating? And, why does it fluctuate?

The fluctuations are simply the variations in scattering between small sub-volumes within a thin sample. These are usually not timevarying fluctuations (although they could be), but instead they are the position-varying fluctuations in local diffraction.

Cross-section transmission electron microscope (TEM) specimen preparation of Ill-V materials using conventional methods can be a painful and time-consuming activity, with a day or more from receipt of a sample to examination in the TEM being the norm. This article describes the cross-section TEM specimen preparation technique used at Bookham Caswell. The usual time from start to finish is <1 hour. Up to 10 samples can be prepared at once, depending upon sample type. Most of the tools used are widely available and inexpensive, making the technique ideal for use in institutions with limited resources.

McDowell and Trump published a seminal paper examining the efficacy of several fixative formulas. They were attempting to determine the best solution for producing samples that could be put in fixative during surgical procedures or in the morgue and then processed for both electron and light microscopy evaluation without significantly compromising either examination method.

When it comes to mineral synthesis, there is a lot we can learn from nature. Although we can synthesize a range of materials in the laboratory, the experimental conditions are often constrained to particular ranges of temperature, pH, etc. Biological systems, on the other hand, seem to be able to produce individual minerals and complex composite mineral structures under a variety of conditions, many of which are far from those applied to create their synthetic counterparts. Understanding how nature does this could provide a means to produce novel biomimetic materials with potential applications in a diverse range of fields from medicine to materials engineering.

Biofilms are communities of microbial cells and extracellular polymeric substances (EPS) attached to a surface. Bacteria exist preferentially in the biofilm state in nature and in many engineered systems. In this state, microbes tolerate antibiotics and disinfectants. Bacterial biofilms are now implicated in a wide range of human diseases and infections including cystic fibrosis, otitis media, chronic wounds, artificial joint and prosthesis infection, and many nosocomial infections. Biofilm-related infections and industrial fouling problems cost billions of dollars each year.

The Field Emission SEM was introduced to improve imaging resolution available with conventional SEMs with a tungsten source. Thermal assisted or Schottky Field Emission SEMs were introduced in s the nineties by a number of companies as a stable source to overcome the beam instability of the cold FESEMs introduced earlier. The Gemini® based Field Emission SEM launched by Zeiss 12 years ago has been designed from the beginning as a high stability FESEM with a relatively large multi-ported chamber. The drive to develop Gemini® technology was the need for a FESEM capable of ultra-high resolution performance over the entire accelerating voltage range that also possessed the flexibility needed for a wide range of analytical applications.

Various fluorescent stains and vital dyes have been used to identify dead cells in animal tissues and celi lines. In plants, fluorescein diacetate and propidium iodide have been used to label nuclei and to identify necrotic cells in plant protoplasts and 4,6-diamidino-2-phenylindole (DAPI) has been used to mark senescing cells in sections of roots. However, these dyes may be problematic when used with intact plant tissue with well-developed cells walls which may impede dye penetration. Endogenous fluorescence has been used to identify dead cells in intact and sectioned plant tissues. Published procedures typically employ ultraviolet (UV) excitation wavelengths of 340-380 nm and emission wavelengths of 400- 425 nm, thus requiring a UV filter set.

One of the capabilities of electron microscopes is to obtain diffraction patterns, which can be analyzed to give information about the structure of the specimen. This brief review discusses some of the technical considerations in using electron diffraction patterns for structural analysis. The technique of selected-area electron diffraction uses diffraction obtained from a limited region of the specimen.

Hexamethyltiisilizane (HMDS) is an excellent method of chemical drying of hydrated specimens. There are several variables involved in its use, the most easily controlled being the number of transitional steps from 100% eihanol (EtOH) to 100% HMDS and the drying temperature.

Fixation and dehydration are the same for both HMDS and CPD. Once thespecimenisinthefinal 100% ethanol, it must then be transferred to 100% HMDS through a graded series of ethanol-HMDS mixtures.