Separation of visibly-excited fluorescent components in fingerprint residue by thin-layer chromatography.

The use of lasers for the detection of fingermarks is widespread in the forensic field. Despite this, and the fact that many studies have been conducted into the composition of fingermark residue, the components responsible for the inherent visible fluorescence remain unidentified. Traditionally compositional studies have been performed on sweat, sebum, or skin surface washes, none of which are truly representative of the situation when a fingerprint is deposited on a surface. In this paper thin-layer chromatography (TLC) has been performed on sebum-rich fingermarks laid directly onto TLC plates and an argon ion laser used to visualize the separated components. It has been found to be a robust and reproducible method for studying the fluorescent components in fingermark residue and is considered to be more realistic than other methods of sample preparation as it eliminates the chances of extraneous matter being extracted from the skin surface. Investigations into the nature of the separated compounds have also been made and the results are reported.

A new visibly-excited fluorescent component in latent fingerprint residue induced by gaseous electrical discharge.

A technique that exposes fingerprint residue to a gaseous electrical discharge in nitrogen followed by treatment with ammonium hydrogen carbonate vapors to produce fluorescence is investigated. Particular attention is made to fluorescence observed via laser illumination at 514 nm. Insight into the nature of the fluorescent components is achieved through the use of thin-layer chromatography (TLC) of fingerprint residue. Results reported indicate the fluorescence observed is from previously non-fluorescent fractions of the fingerprint residue, and TLC results point towards lipid derivatives as a possible source of the fluorescence.

The effects of fingermark enhancement light sources on subsequent PCR-STR DNA analysis of fresh bloodstains.

This paper describes a study designed to investigate the effects of light sources used to enhance fingermarks on the subsequent polymerase chain reaction (PCR)-short tandem repeat (STR) analysis of bloodstains. Dried bloodstains on glass were exposed for up to 30 min to five different light sources: Argon ion laser, Polilight UV, Polilight green, Superlite, and shortwave UV. The bloodstains were subsequently analyzed using a quadruplex PCR system. It was found that treating the bloodstains with four of the five light sources had no appreciable effect on the results obtained from subsequent PCR analysis. However, exposure of the bloodstains to shortwave UV light for more than 30 s precluded the acquisition of results from PCR testing. Therefore, under casework conditions, it would be preferable to avoid exposing bloodstains, on which PCR typing is to be performed, to shortwave UV.

Fluorescence spectroscopy as an aid to imaging latent fingermarks in the ultraviolet.

Two- and three-dimensional fluorescence spectroscopic data have been recorded from sebum-rich latent fingermarks on quartz and white card. The fingermark residue was found to fluoresce between 310 to 380 nm and have an excitation range between 260 to 300 nm. The data are used to describe the results observed when imaging the inherent ultraviolet photoluminescence of latent fingermarks.

Control of Culex quinquefasciatus in pit latrines, using shredded, waste polystyrene.

As an alternative to the use of commercially available, expanded-polystyrene beads, a study was made of the effectiveness of shredded, waste polystyrene (SWAP) for the control of Culex quinquefasciatus. The relevant physical properties of the SWAP were first investigated in the laboratory. Then, under field conditions in wet pit latrines, mosquito emergence rates were measured before and after application of the material. In the laboratory, when compared with the commercial product, the irregular shape of the SWAP particles greatly reduced their capacity to spread over the water surface and the interstitial air spaces also permitted respiration and development of mosquito larvae. Nevertheless, under field conditions, with careful application of the SWAP over the water surfaces in wet pit latrines, almost complete control of mosquito breeding was observed within a few days. This was sustained for 60 days, at which time observations were discontinued. SWAP appears to offer an effective, cheap and readily available alternative to the commercial product for the control of C. quinquefasciatus. The practicality of using it in community-based, mosquito-control programmes warrants further study.

Control of Culex quinquefasciatus in pit latrines, using shredded, waste polystyrene

As an alternative to the use of commercially available, expanded-polystyrene beads, a study was made of the effectiveness of shredded, waste polystyrene (SWAP) for the control of Culex quinquefasciatus. The relevant physical properties of the SWAP were first investigated in the laboratory. Then, under field conditions in wet pit latrines, mosquito emergence rates were measured before and after application of the material. In the laboratory, when compared with the commercial product, the irregular shape of the SWAP particles greatly reduced their capacity to spread over the water surface and the interstitial air spaces also permitted respiration and development of mosquito larvae. Nevertheless, under field conditions, with careful application of the SWAP over the water surfaces in wet pit latrines, almost complete control of mosquito breeding was observed within a few days. This was sustained for 60 days, at which time observation were discontinued. SWAP appears to offer an effective, cheap and readily available alternative to the commercial product for the control of C. quinquefasciatus. The practicality of using it in community-based, mosquito-control programmes warrants further study.(AU)

Ultraviolet luminescence from latent fingerprints.

Illumination of latent fingerprints on white paper using 266-nm radiation from a Nd:YAG laser and photographic detection of their ultraviolet fluorescence, produces images with good ridge detail. The detection rate was 69% in a survey of fingerprints from 34 people compared with only 23% using an argon-ion laser at 514 nm. Prolonged exposure to UV light decreased the inherent UV fluorescence intensity but no adverse effects were observed on subsequent treatment with 1,8-diazafluoren-9-one or ninhydrin.

Catecholamine responses to histamine infusion in man.

To evaluate the effects of histamine-induced hypotension on plasma catecholamine levels, eight normal men, aged 20 to 40 years, were infused with incremental doses of histamine starting at 0.2 microgram/kg/min at a 30 degree tilt position with monitoring of blood pressure (BP) and heart rate. Histamine dosage was increased every 5 minutes by 0.1 to 0.2 microgram/kg/min until mean BP fell greater than 15 mm Hg or a dosage of 1.6 micrograms/kg/min was reached. Plasma catecholamine samples were taken between the fourth and fifth minute of each histamine dosage. Identical measurements were made during nitroglycerin-induced hypotension in these subjects. Histamine produced threefold greater increases in heart rate and plasma norepinephrine (NE) levels than did nitroglycerin for comparable decreases in BP. Although NE levels increased twofold to fivefold from baseline with histamine infusion, epinephrine levels increased minimally at the highest doses or not at all. Our data demonstrate that histamine selectively releases NE from adrenergic nerve terminals without significant adrenal catecholamine release. We suggest that neural NE release plays an important role in the cardiac effects of histamine.