No abstract

Blood is one of the most commonly encountered types of biological evidence found at scenes of violent crime and one of the most commonly observed fingerprint contaminants. Current visualisation methods rely on presumptive tests or chemical enhancement methods. Although these can successfully visualise ridge detail, they are destructive, do not confirm the presence of blood and can have a negative impact on DNA sampling. A novel application of visible wavelength reflectance hyperspectral imaging (HSI) has been used for the detection and positive identification of blood stained fingerprints in a non-contact and non-destructive manner on white ceramic tiles. The identification of blood was based on the unique visible absorption spectrum of haemoglobin between 400 and 500 nm. HSI has been used to successfully visualise ridge detail in blood stained fingerprints to the ninth depletion. Ridge detail was still detectable with diluted blood to 20-fold dilutions. Latent blood stains were detectable to 15,000-fold dilutions. Ridge detail was detectable for fingerprints up to 6 months old. HSI was also able to conclusively distinguish blood stained fingerprints from fingerprints in six paints and eleven other red/brown media with zero false positives.

Biological samples, such as blood, are regularly encountered at violent crime scenes and successful identification is critical for criminal investigations. Blood is one of the most commonly encountered fingerprint contaminants and current identification methods involve presumptive tests or wet chemical enhancement. These are destructive however; can affect subsequent DNA sampling; and do not confirm the presence of blood, meaning they are susceptible to false positives. A novel application of visible wavelength reflectance hyperspectral imaging (HSI) has been used for the non-contact, non-destructive detection and identification of blood stained fingerprints across a range of coloured substrates of varying porosities. The identification of blood was based on the Soret γ band absorption of haemoglobin between 400 nm and 500 nm. Ridge detail was successfully visualised to the third depletion across light coloured substrates and the stain detected to the tenth depletion on both porous and non-porous substrates. A higher resolution setup for blood stained fingerprints on black tiles, detected ridge detail to the third depletion and the stain to the tenth depletion, demonstrating considerable advancements from previous work. Diluted blood stains at 1500 and 1000 fold dilutions for wet and dry stains respectively were also detected on pig skin as a replica for human skin.

The composition of fingerprints can contain a wealth of information with regard to the donor of the fingerprint. Fatty acids and other related sebaceous materials can be used to classify donor groups, as previously reported. The extraction of these particular materials from the fingerprint entities has proven to be rather tedious and difficult to reproduce on standardised samples. We present a two step method to obtain a broad spectrum of sebaceous materials from fingerprints in high yields with good reproducibility. By dissolving the fingerprint material in MeOH in the presence of TMSCl the fatty acids are esterified to their corresponding fatty acid methyl esters. During this extraction some of the other sebaceous materials are extracted as well. Only in a consecutive extraction with CHCl 3 is an optimal extraction of the fatty content of a fingerprint achieved.

Bloodstains are often encountered at scenes of violent crime and have significant forensic value for criminal investigations. Blood is one of the most commonly encountered types of biological evidence and is the most commonly observed fingerprint contaminant. Presumptive tests are used to test blood stain and blood stained fingerprints are targeted with chemical enhancement methods, such as acid stains, including Acid Black 1, Acid Violet 17 or Acid Yellow 7. Although these techniques successfully visualise ridge detail, they are destructive, do not confirm the presence of blood and can have a negative impact on DNA sampling. A novel application of visible wavelength hyperspectral imaging (HSI) is used for the noncontact, non-destructive detection and identification of blood stained fingerprints on white tiles both before and after wet chemical enhancement using Acid Black 1. The identification was obtained in a non-contact and non-destructive manner, based on the unique visible absorption spectrum of haemoglobin between 400 and 680 nm. Results from the exploration of the selectivity of the setup to detect blood against ten other non-blood protein contaminants are also presented. A direct comparison of the effectiveness of HSI with chemical enhancement using Acid Black 1 on white tiles is also presented.

No abstract

The ability to establish the exact time a crime was committed is one of the fundamental aims of forensic science. The analysis of recovered evidence can provide information to assist in age determination, such as blood, which is one of the most commonly encountered types of biological evidence and the most common fingerprint contaminant. There are currently no accepted methods to establish the age of a blood-stained fingerprint, so progress in this area would be of considerable benefit for forensic investigations. A novel application of visible wavelength reflectance, hyperspectral imaging (HSI), is used for the detection and age determination of blood-stained fingerprints on white ceramic tiles. Both identification and age determination are based on the unique visible absorption spectrum of haemoglobin between 400 and 680 nm and the presence of the Soret peak at 415 nm. In this study, blood-stained fingerprints were aged over 30 days and analysed using HSI. False colour aging scales were produced from a 30-day scale and a 24 h scale, allowing for a clear visual method for age estimations for deposited blood-stained fingerprints. Nine blood-stained fingerprints of varying ages deposited on one white ceramic tile were easily distinguishable using the 30-day false colour scale.