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Examination of Firearms Review: 2007 to 2010 - Interpol

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Morgan et al [43] studied the statistical validity <strong>of</strong> discrimination between<br />

various polymer classes and dyed textile fibres, visualisation <strong>of</strong> significant<br />

differences between groups <strong>of</strong> spectra discrimination, and tracking <strong>of</strong> spectral<br />

changes with environmental changes. Fibres and associated spectra<br />

contained in the database, combined with validated s<strong>of</strong>tware, are useful for<br />

fibre comparisons in casework and for quality control and the training <strong>of</strong><br />

analysts. This paper describes the application <strong>of</strong> linear discriminant analysis<br />

<strong>to</strong> a database containing more than 5,000 UV/visible absorbance and<br />

fluorescence spectra.<br />

Abendshien et al [44] Reported on the development <strong>of</strong> the FBI Forensic<br />

Au<strong>to</strong>motive Carpet Fibre Identification Database (FACID). At present, FACID<br />

contains more than 700 au<strong>to</strong>motive carpet samples from private vehicles and<br />

vehicle manufacturers. Questioned carpet-type fibres can be searched by<br />

microscopic characteristics, fibre type, and/or colour information in order <strong>to</strong><br />

determine whether or not a particular type <strong>of</strong> vehicle was involved in the<br />

commission <strong>of</strong> a crime. FACID can also be searched by vehicle make, model,<br />

year, and/or colour in order <strong>to</strong> determine the carpet samples available for<br />

comparison.<br />

Ali et al [45] this study, a natural dye extracted from Eucalyptus camaldulensis<br />

was used <strong>to</strong> colour cot<strong>to</strong>n fabric by direct dyeing under a range <strong>of</strong> different<br />

conditions. The aim <strong>of</strong> this work was <strong>to</strong> compare the fastness properties <strong>of</strong><br />

dyeing by different dyeing techniques. This dye shows fairly good saturation<br />

on cot<strong>to</strong>n and has medium-<strong>to</strong>-good fastness properties.<br />

Morgan et al [46] assessed whether forensic fibre discrimination could be<br />

improved by extracting the dye from the fibre prior <strong>to</strong> trace analysis by a highresolution<br />

separation technique. Methods developed for the extraction <strong>of</strong><br />

unknown dyes from fibres, were based on three capillary electrophoresis (CE)<br />

procedures for dyes from six classes <strong>of</strong> textile dyes. CE with diode array<br />

detection is useful for the analysis <strong>of</strong> longer-length fibres, but a more sensitive<br />

and selective method, such as CE/mass spectrometry (MS) is required for the<br />

analysis <strong>of</strong> the small amount <strong>of</strong> dye (2-200 ng) associated with forensically<br />

relevant fibre samples. The analytical approach was destructive, but only an<br />

extremely small sample (approx. 2 mm <strong>of</strong> a single 15-um diameter fibre) was<br />

required. CE/MS analysis was found <strong>to</strong> be capable <strong>of</strong> separating extracted<br />

dye components and providing semi-quantitative estimates <strong>of</strong> dye amounts<br />

whilst providing qualitative information for the identification <strong>of</strong> dyes.<br />

Eng and Bhagwandin [47] investigated the effect <strong>of</strong> metamerism in the<br />

generation <strong>of</strong> different UV-visible spectra. Metameric samples <strong>of</strong> blue textile<br />

fibres, created using different colouring agents or different relative<br />

concentrations <strong>of</strong> the colouring agents, were examined in order <strong>to</strong><br />

demonstrate their differentiation based on their spectra between 350 and 800<br />

nm using UV-visible microspectropho<strong>to</strong>metry. It was found that some <strong>of</strong> the<br />

metameric samples intersected at three or more loci, but some did not<br />

intersect at all. In the intersecting spectra, there was no correlation between<br />

either the dye chemistries <strong>of</strong> the relative component concentrations.<br />

194

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