Experiences in successive forensic analysis of GSR and DNA traces collected on a single tape lift stub.

Gunshot residue (GSR) and deoxyribonucleic acid (DNA) analyses are used in the reconstruction of shooting incidents involving firearms. In both fields, adhesive tapes are commonly applied to recover traces. Using a simultaneous sampling approach for retrieving both types of traces from objects related to a shooting can be powerful.

Objectifying evidence evaluation for gunshot residue comparisons using machine learning on criminal case data.

Comparative gunshot residue analysis addresses relevant forensic questions such as 'did suspect X fire shot Y?'. More formally, it weighs the evidence for hypotheses of the form H: gunshot residue particles found on suspect's hands are from the same source as the gunshot residue particles found on the crime scene and H: two sets of particles are from different sources. Currently, experts perform this analysis by evaluating the elemental composition of the particles using their knowledge and experience.

Comparison of GSR composition occurring at different locations around the firing position.

Variations in gunshot residue (GSR) compositions are used in the reconstruction of shooting incidents. In this study, GSR samples taken from seven different locations around and in the firearm were collected and analyzed using scanning electron microscopy/energy dispersive X-ray analysis. Four different types of ammunition were applied.

The ring structure and organization of light harvesting 2 complexes in a reconstituted lipid bilayer, resolved by atomic force microscopy.

The main function of the transmembrane light-harvesting complexes in photosynthetic organisms is the absorption of a light quantum and its subsequent rapid transfer to a reaction center where a charge separation occurs. A combination of freeze-thaw and dialysis methods were used to reconstitute the detergent-solubilized Light Harvesting 2 complex (LH2) of the purple bacterium Rhodopseudomonas acidophila strain 10050 into preformed egg phosphatidylcholine liposomes, without the need for extra chemical agents. The LH2-containing liposomes opened up to a flat bilayer, which were imaged with tapping and contact mode atomic force microscopy under ambient and physiological conditions, respectively.