The recoverability of fingerprints on paper exposed to elevated temperatures - Part 1: comparison of enhancement techniques

This research investigates the recoverability of fingerprints which have been exposed to elevated temperatures in order to mimic the environment a piece of paper may be exposed to within an arson scene. Arson is an expensive crime, costing the UK economy, on average, £53.8 million each week [1]. Anything which may give rise to the identity of the fire setter should be analysed and as such, unburnt paper may be a potential source of fingerprints. While it is true that even a moderate fire will obscure and render partially useless some types of evidence, many items, including fingerprints, may still survive [2-4]. This research has shown that fingerprints are still retrievable from paper which has been subjected to the maximum testing conditions of 200˚C for 320min. In fact, some fingerprints naturally enhance themselves by the heating process. This investigation has also shown that the most effective enhancement technique was found to be 1,8-diazafluoren-9-one (DFO) for exposure temperatures upto 100˚C. Physical developer (PD) is the most effective enhancement technique for exposure temperatures from 100˚C to 200˚C. For porous surfaces, there are fingerprint development techniques which are effective at enhancing fingerprints exposed upto a temperature of 200˚C, irrespective of the firefighting extinguishing technique, as PD, in addition to developing fingerprints exposed to high temperatures, is one of the few processes which will enhance fingermarks on wetted surfaces

The recoverability of fingerprints on paper exposed to elevated temperatures - Part 2: natural fluorescence

Previous work by the authors [1] investigated the recoverability of fingerprints on paper which had been exposed to elevated temperatures by comparing various chemical enhancement techniques (ninhydrin, 1,8-diazafluoren-9-one (DFO), and physical developer (PD)). During that study, it became apparent, as a consequence of observations made in operational work [2], that fingerprints on paper subjected to 150˚C fluoresced under examination with green light of waveband 473-548nm with a 549nm viewing filter. This work examined the three types of prints (eccrine, sebaceous, and ungroomed) after 20 min exposure to the temperature range 110˚C to 190˚C (in 10˚C increments) and found that the eccrine fingerprints fluoresced more brightly. This indicated that it was a component of the eccrine deposit which was causing the fluorescence. Luminance measurements found that the maximum fluorescence was experienced at 170˚C on both types of paper. As a consequence, eccrine heat-treated fingerprints were viewed under violet-blue (350-469nm), blue (352-509nm), and green light (473-548nm) which indicated that the greatest luminance intensities were obtained under blue light and the smallest under green light. In order to determine what component of the eccrine fingerprint was causing this fluorescence, five of the most prevalent amino acids (alanine, aspartic acid, glycine, lysine, and serine) [3-4] were exposed to this temperature range. The luminance measurements were taken under exposure to the green light in order for the minimum fluorescence to be observed, with an assumption that blue-violet or blue illumination will provide brighter fluorescence in practice. The results indicated that four of the amino acids are behaving similarly across the temperature range, but with slightly different luminance measurements, but all are exhibiting some level of fluorescence. Thermal degradation products of alanine and aspartic acid have been suggested by Richmond-Aylor et al. [5]. The structure of these thermal degradation products is cyclic in nature, and as such, there is a possibility that two of these products would fluorescence. Sodium chloride and urea were also exposed to the temperature range and they also fluoresced to some extent. This work shows that eccrine fingerprints that have been exposed to temperatures of between 130˚C to 180˚C will fluoresce under violet-blue, blue, and green light. This level of fluorescence for ungroomed fingerprints is much less but this will be dependent on the individual, the more eccrine the deposit, the stronger the fluorescence. This work shows that the amino acids, sodium chloride, and urea present in fingerprint deposits are all contributing to the fluorescence of the print, but may not be the sole contributor as other eccrine components have not yet been tested

The visualisation of fingermarks on Pangolin scales using gelatine lifters

Recent media reports document the plight of the Pangolin and its current position as “the most trafficked mammal in the world”. They are described by some as scaly anteaters as all species are covered in hard keratinous tissue in the form of overlapping scales acting as a “flexible dermal armour”. It is estimated that between 2011 and 2013, 117,000–234,000 pangolins were slaughtered, but the seizures may only represent as little as 10% of the true volume of pangolins being illegally traded. In this paper, methods to visualise fingermarks on Pangolin scales using gelatine lifters is presented. The gelatine lifters provide an easy to use, inexpensive but effective method to help wildlife crime rangers across Africa and Asia to disrupt the trafficking. The gelatine lifting process visualised marks producing clear ridge detail on 52% of the Pangolin scales examined, with a further 30% showing the impression of a finger with limited ridge detail. The paper builds on an initial sociotechnical approach to establishing requirement, then it focuses on the methods and outcomes relating to lifting fingermarks off Pangolin scales using gelatine lifters, providing an evaluation of its use in practice

The visualisation on Pangolin scales using gelatine lifters

Recent media reports document the plight of the Pangolin and its current position as “the most trafficked mammal in the world”. They are described by some as scaly anteaters as all species are covered in hard keratinous tissue in the form of overlapping scales acting as a “flexible dermal armour”. It is estimated that between 2011 and 2013, 117,000 to 234,000 pangolins were slaughtered, but the seizures may only represent as little as 10% of the true volume of pangolins being illegally traded. In this paper, methods to visualise fingermarks on Pangolin scales using gelatine lifters is presented. The gelatine lifters provide an easy to use, inexpensive but effective method to help wildlife crime rangers across Africa and Asia to disrupt the trafficking. The gelatine lifting process visualised marks producing clear ridge detail on 52% of the Pangolin scales examined, with a further 30% showing the impression of a finger with limited ridge detail. The paper builds on an initial sociotechnical approach to establishing requirement, then it focuses on the methods and outcomes lifting fingermarks off Pangolin scales using gelatine lifters, providing an evaluation of the viability of using the lifters in practice

Home Office Fingerprint Source Book

The Fingerprint Source Book is primarily intended to provide the background and validation for the techniques currently (up to 2016) recommended by the Home Office Centre for Applied Science and Technology (CAST), and to publish, in some cases for the first time, data collected over 45 years of research. It will therefore often present information in an ‘CASTcentric’ way, emphasising research that was carried out at Sandridge or Horseferry House, possibly sometimes at the expense of research carried out elsewhere. It is not the intention of the authors to ignore the significant contributions made by other research groups and apologies are made in advance if this sometimes appears to be the case. The document is also aimed at providing the UK Forensic Science Regulator and the United Kingdom Accreditation Service (UKAS), which has carried out ISO 17025 accreditation in the UK, with the background evidence behind the advice given in the Fingermark Visualisation Manual

The Reed-Stanton press rig for the generation of reproducible fingermarks : towards a standardised methodology for fingermark research

In the search for better or new methods/techniques to visualise fingermarks or to analyse them exploiting their chemical content, fingermarks inter-variability may hinder the assessment of the method effectiveness. Variability is due to changes in the chemical composition of the fingermarks between different donors and within the same donor, as well as to differential contact time, pressure and angle. When validating a method or comparing it with existing ones, it is not always possible to account for this type of variability. One way to compensate for these issues is to employ, in the early stages of the method development, a device generating reproducible fingermarks. Here the authors present their take on such device, as well as quantitatively describing its performance and benefits against the manual production of marks. Finally a short application is illustrated for the use of this device, at the method developmental stages, in an emerging area of fingerprinting research concerning the retrieval of chemical intelligence from fingermarks

Filarial Parasites Develop Faster and Reproduce Earlier in Response to Host Immune Effectors That Determine Filarial Life Expectancy

During larval development, filarial nematodes adjust their lifelong reproductive strategy to the presence of anti-parasitic immune cells that determine host resistance and experimental vaccine efficacy

Understanding Human-Plasmodium falciparum Immune Interactions Uncovers the Immunological Role of Worms

BACKGROUND: Former studies have pointed to a monocyte-dependent effect of antibodies in protection against malaria and thereby to cytophilic antibodies IgG1 and IgG3, which trigger monocyte receptors. Field investigations have further documented that a switch from non-cytophilic to cytophilic classes of antimalarial antibodies was associated with protection. The hypothesis that the non-cytophilic isotype imbalance could be related to concomittant helminthic infections was supported by several interventions and case-control studies. METHODS AND FINDINGS: We investigated here the hypothesis that the delayed acquisition of immunity to malaria could be related to a worm-induced Th2 drive on antimalarial immune responses. IgG1 to IgG4 responses against 6 different parasite-derived antigens were analyzed in sera from 203 Senegalese children, half carrying intestinal worms, presenting 421 clinical malaria attacks over 51 months. Results show a significant correlation between the occurrence of malaria attacks, worm carriage (particularly that of hookworms) and a decrease in cytophilic IgG1 and IgG3 responses and an increase in non-cytophilic IgG4 response to the merozoite stage protein 3 (MSP3) vaccine candidate. CONCLUSION: The results confirm the association with protection of anti-MSP3 cytophilic responses, confirm in one additional setting that worms increase malaria morbidity and show a Th2 worm-driven pattern of anti-malarial immune responses. They document why large anthelminthic mass treatments may be worth being assessed as malaria control policies

Volatilised pyrene: A phase 1 study demonstrating a new method of visualising fingermarks with comparisons to iodine fuming

Pyrene is a fluorescent polycyclic aromatic hydrocarbon that can be volatilised under mild conditions. When fumed, pyrene is rapidly absorbed into the sebaceous residues of fingermarks, enabling their fluorescent visualisation upon excitation with ultraviolet radiation. This new means of fluorescent fingermark detection is more sensitive than the non-fluorescent iodine fuming approach for nonporous surfaces. This is demonstrated here in a phase 1 study using split-print comparisons on metal and glass surfaces. Pyrene-treated fingermarks also retain the volatile fluorophore for comparably long time periods relative to iodine fuming (in the order of hours). The phase 1 study comprised four donors, and 80 natural fingermarks that were grouped into two time periods; aged 24 h and 1 week. Iodine fuming was chosen as a reference to showcase the effectiveness of pyrene given it is the most closely-related chemical fuming method in routine use. This study demonstrates that pyrene fuming increases the quantity and quality of fingermark visualisations relative to iodine fuming, and is free of many of the latter method’s drawbacks. Preliminary results shown here also show the effectiveness of pyrene fuming on highly patterned surfaces, and its compatibility with the use of gelatine lifters. Pyrene fuming is thus easy to effect, low-cost, and shows great promise as a new means of visualising fingermarks on non-porous surfaces