Environmental assessment of gunshot residue particles in the public domain of the United Kingdom.

Only limited data currently exists on the inadvertent transfer of gunshot residue (GSR), or GSR-like particles through contact with public places. In this study, an assessment occurrence of GSR in public environments in England, UK was undertaken. Utilizing a stubbing sampling technique over 260 samples were collected from areas accessible to the public, including buses, trains, taxis, and train stations. Stub analysis was performed by Scanning Electron Microscopy with Energy Dispersive X-ray Analysis (SEM-EDX). The results showed no characteristic GSR particles were detected on any of the 262 samples taken. From these samples, a total of four indicative/consistent particles were identified on one train seat (2× BaAl, 2× PbSb). Although geographical location and firearm association is likely to influence GSR occurrence, the data suggests that the potential for inadvertent GSR transfer through contact with public transport and associated communal areas is insignificant. Further research assessing environmental background levels of GSR in additional geographical locations is critical in an evaluation of the potential for GSR transfer from the environment.

Vacuum metal deposition enhancement of friction ridge detail on ballistic materials.

The efficacy of Gold/Zinc and Silver/Zinc vacuum metal deposition (VMD) protocols were assessed as stand-alone methods of fingermark enhancement on ballistic brass materials. The results demonstrate the effectiveness of VMD enhancement on a large pool of donors (n = 20), with potentially identifiable marks recovered for the majority of donors, including samples aged up to two months. Of the 20 donors a subset of six donors were selected to assess the capability of VMD enhancement on brass fired cartridge cases, from which some friction ridge detail (FRD) was recovered. Lastly, an attempt to understand which fingermark components are facilitators of VMD enhancement was made. Fingermark residue was extracted from brass tiles and fired cartridge cases before analysing chromatographically (GC-MS). Although some key components were indicated, further evaluation of all fingermark components is needed to draw firm conclusions as to the role each plays in VMD enhancement.

Pesticides in cannabis: A review of analytical and toxicological considerations.

A review of the literature surrounding the use, analysis, and detection of pesticide material for cannabis cultivation is presented. The use of pesticides in crop cultivation is not new, and cannabis crops are no exception. Studies have found that the use of these are common and that high levels of the pesticides are transferred into the cannabis smoke. The most common pesticide classes associated with cannabis are insecticides, acaricides, and fungicides. Over 350 different pesticide products may be used on cannabis materials and of these, 16 pesticides and three plant growth regulators (PGR) are considered to be the main candidates. Many of the pesticides found in cannabis samples destined for consumption are classed as moderately hazardous by the World Health Organization. Analytical methods for pesticide detection on cannabis are being developed with a view to implementing quality control of cannabis, where it is legal, before being sold. However, no standardized protocol exists. The pesticide levels found in the cannabis samples tested were generally low (less than µg/g), these results do not, however, provide information on chronic low-dose adverse effects of pesticides in relation to cannabis consumption. Currently no research exists on the toxicity of pyrolyzed pesticides in humans from smoking cannabis. More studies are needed to further understand this potentially harmful health threat.

Fate and Behavior of Gunshot Residue: Recreational Shooter Vehicle Distribution.

The susceptibility for recreational shooters to transfer gunshot residue (GSR) to both the interior and exterior of a vehicle is investigated. A comprehensive sampling protocol was used to assess the most likely areas of GSR transfer from recreational shooter contact, such as the steering wheel and the area, the firearms were stored (the trunk). Up to 315 characteristic GSR, particles were found in several locations throughout the interior of a vehicle. As many as 876 characteristic particles were found throughout a single vehicle. The data indicate that vehicles frequently occupied by firearms users are a potential source for inadvertent transfer of GSR to persons unrelated to firearm activity. In criminal cases where vehicles have been used, such transfer processes for GSR need to be considered within the context of any case interpretation. The implications for subsequent contamination and transfer processes from such vehicles require further investigation.

The analysis of organic and inorganic gunshot residue from a single sample.

The detection and interpretation of gunshot residue (GSR) can play an important role in the investigation of firearm related incidents. Recently, the potential of organic compounds to provide an additional means to discriminate between GSR and environmental particles, in particular in cases where lead-free ammunition is used, has been highlighted. This work describes a method for the extraction and detection of complementary organic and inorganic compounds from a single GSR sample, using a methodology that makes implementation in the current standard procedure feasible. GSR samples were collected from the shooter's hands following double and single discharges, using the traditional adhesive carbon aluminium stubs. Analysis of organic compounds was performed using solid-phase microextraction gas chromatography mass spectrometry (SPME-GC-MS), followed by analysis of the traditional inorganic particles using scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDX). Detection of both categorised organic GSR compounds (e.g. ethyl centralite, diphenylamine and 2-nitrodiphenylamine) and characteristic inorganic GSR has been achieved. Given the fact that the detected organic GSR compounds are relevant with respect to the confirmation of GSR materials, this method has successfully demonstrated the ability to obtain a total chemical profile from a single GSR sample, which has the potential to increase the probative value of GSR evidence.

A Preliminary Study on Vacuum Metal Deposition as a Standalone Method for Enhancement of Fingermarks on Ballistic Brass Materials.

In order to assess the efficacy of vacuum metal deposition (VMD) as a technique to develop fingermarks on ballistic metallic surfaces, a preliminary study using six donors (three male & three female) was conducted. Using a sequential metal deposition process, two metal combinations were studied-gold/zinc and silver/zinc. Results indicate the potential of this technique, by developing identifiable fingermarks on brass metal disks aged from a few days up to more than a month old. As the development of fingermarks on fired (brass) cartridge cases is an area of interest, a further study was conducted where a total of 20 fingermarks were deposited on cases. After firing, second level fingermark characteristics were successfully observed on cartridge cases highlighting its potential as a fingermark enhancement method for ballistic brass materials. Further work is required to fully evaluate the VMD process and its reliability as a fingermark enhancing method on ballistic surfaces.

Detection of Fingermarks-Applicability to Metallic Surfaces: A Literature Review.

There are many different fingermark visualization techniques available, and the choice of methodology employed may be dependent on the surface type. This comprehensive review of the scientific literature evaluates the methodologies of fingermark enhancement methods that are applicable to metallic surfaces; optical, physical, chemical, and physicochemical methods are critically discussed. Methods that are currently used and those that have the potential to reduce the cost and time required to process evidence and increase the recovery rates are considered and are assessed against the Centre for Applied Science and Technology (CAST) and the International Fingerprint Research Group (IFRG) guidelines. The use of chemical imaging techniques in particular has increased the potential to recover fingermarks of sufficient quality for identification purposes. Presently, there appears to be a lack of detailed research pertaining to validation and thorough casework studies for fingermark enhancement techniques. Further studies incorporating these guidelines are recommended.

Fate and Behavior of Gunshot Residue-A Review.

A review of the literature concerning the fate and behavior of gunshot residue (GSR) is presented. A number of concomitant parameters including firearm and ammunition type, plume and GSR material characteristics, travel distances, chemical composition and GSR morphology are critically discussed in relation to their effects on the distribution and deposition, transfer and persistence processes of GSR. The underlying mechanisms associated with such processes are also considered. Knowledge of these processes on GSR materials could provide valuable information concerning scene preservation and subsequent forensic sampling. The number of GSR particles deposited can vary significantly with each firearm discharge, highlighting the potential to produce distinctive data in each individual case. With the continual development and compositional changes of new ammunition types, further evaluation of the effect these processes may have on GSR evidence and their possible influence on the interpretation of the analytical results should be given due consideration.

Preliminary classification of characteristic organic gunshot residue compounds.

For the first time, a classification system for organic gunshot residue (OGSR) compounds with respect to the confirmation of OGSR materials is presented. There are 136 compounds considered to be associated with OGSR that have been highlighted in the literature. Many of these compounds could be classified as being ubiquitous in the environment and thus their detection as characteristic components of OGSR could cause issues with the interpretation of chemical ballistic evidence. The proposed system aims to address this problem by classifying OGSR compounds based on their forensic relevance with respect to the confirmation of GSR materials. To increase the forensic relevance of such a system, the large number of OGSR compounds reported in the literature has been decreased to 20 OGSR compounds based on the organic chemical composition of over 200 propellant powders. Occupational and environmental materials also associated with OGSR compounds have been considered.

Injection port silylation of γ-hydroxybutyrate and trans-hydroxycrotonic acid: conditions optimisation and characterisation of the di-tert-butyldimethylsilyl derivatives by GC-MS.

Silylation is usually carried out on γ-hydroxybutyrate (GHB) for its analysis by Gas Chromatography/Mass Spectrometry (GCMS) and requires potentially long incubation times before injection during which the derivatisation reagent and derivatives (such as trimethyl-silyl compounds) can hydrolyse. Moreover, alternative internal standards (IS) are often useful depending on sample matrices, extraction/purification procedures, commercial availability and price. This study evaluated the possibility of silylating GHB with an injection port derivatisation procedure using N-methyl-N-[tert-butyldimethyl-silyl]trifluoroacetimide (MTBSTFA) with 1% tert-butyldimethylchlorosilane (TBCS) as the derivatisation reagent, producing di-tert-butyldimethyl-silyl derivatives as a novel means of analyzing GHB. In parallel, trans-hydroxycrotonic acid (t-HCA) was investigated as a potential IS for GHB quantification. Analyses were carried out with a temperature programmable injector and the GHB(t-BDMS)(2) and t-HCA(t-BDMS)(2) derivatives were successfully produced, characterised and derivatisation conditions optimised. t-HCA behaved very similarly to GHB through the derivatisation processes and was used as the IS for the determination of urinary endogenous GHB concentrations in human subjects where the method showed a limit of detection of 0.049 µg mL(-1), a limit of quantification of 0.162 µg mL(-1), and a limit of confirmation of 1.33 µg mL(-1), suitable for toxicological GHB concentration determination.

The evaluation of solid phase micro-extraction fibre types for the analysis of organic components in unburned propellant powders.

This work describes the evaluation of various solid phase micro-extraction (SPME) fibre types for the detection of compounds originating from particles of unburned propellant powders. These compounds may also be found in association with organic gunshot residues (OGSR). Seven SPME fibres were assessed based on their ability to extract the compounds of interest (diphenylamine (DPA), 4-nitrodiphenylamine (4-NDPA), ethyl centralite (EC), nitroglycerin (NG) and dibutyl phthalate (DBP)) from four ammunition types across three calibres (9 mm, 5.56 mm and 7.62 mm). Extracts were analysed by gas chromatography/mass spectrometry (GC/MS). Results indicated that the 65 µm polydimethylsiloxane/divinylbenzene (PDMS/DVB) was the most suitable fibre type for the extraction of these compounds across the ammunition types tested. Optimal extraction time parameters were also assessed with a 35-min period determined to be suitable. A number of previously unreported considerations for extracting propellant powders and potentially OGSR related materials are discussed.

Analysis of gunshot residue and associated materials--a review.

A comprehensive review of the scientific literature on gunshot residue (GSR) is presented. Aspects of both inorganic and organic GSR are discussed, from formation and distribution, to sample collection, preparation, and analysis using a variety of techniques. The interpretation of GSR results is also considered including issues surrounding the contamination, distribution, and transfer of GSR. Potential problems with ulterior sources of GSR like particles have been reported in the literature. For example, particles from environmental and occupational sources have been highlighted as exhibiting similar chemical and morphological characteristics to GSR. These findings are put into context with regard to interpreting samples. A move toward a "case by case" approach is argued to be more preferable to a "formal" classification system where possible. The analysis of both inorganic and organic compositions of residue samples as well as morphological considerations is considered to be a more ideal approach to GSR analysis, wherever practicable.

Modelling the long-term fate of mercury in a lowland tidal river. II. Calibration and comparison of two models with field data.

This study presents results of the application of two-one-dimensional/dynamic-deterministic models developed to evaluate and predict mercury contamination of a lowland river, the River Yare, Norfolk, UK. As a general indication of model performance, MODEL 1 produced a prediction of the overall mass balance of mercury in the River Yare that was 6% lower than an estimate, based on measurements, and 10% lower than the prediction provided by MODEL 2. The mercury surficial sediment concentrations calculated by MODEL 1 varied from 0.46 mg kg(-1) in 1995 (Reach 3) to 3.55 mg kg(-1) in 1986 (Reaches 6 and 7), whereas the minimum mercury concentration calculated by MODEL 2 was 0.42 mg kg(-1) in 1995 (Reach 3) and the maximum was 8.45 mg kg(-1) in 1986 (Reach 5). Average mercury concentrations experimentally measured in surficial sediments ranged from 0.47 mg kg(-1) in 1995 (Reach 3) to 8.10 mg kg(-1) in 1986 (Reach 6). MODEL 2 gave an excellent prediction of mercury in fish flesh compared with the results obtained from the actual analysis of fish flesh. Both models demonstrated good ability to simulate actual values determined for all compartments, water, surficial sediments, bottom sediments, and fish.

Modelling the long-term fate of mercury in a lowland tidal river. I. Description of two finite segment models.

Crucial determinants of the potential effects of mercury in aquatic ecosystems are the speciation, partitioning, and cycling of its various species. These processes are affected by site-specific factors, such as water chemistry, sediment transport, and hydrodynamics. This study presents two different approaches to the development of one-dimensional/dynamic-deterministic models for the evaluation and prediction of mercury contamination in a lowland tidal river, the River Yare (Norfolk, UK). The models described here were developed to encompass the entire river system and address the mass balance of mercury in a multicompartment system, including tidal reversal and saline limit. The models were focused on river systems, with the River Yare being used as a case study because previous modelling studies have been centred on lakes and wetlands whilst there is a paucity of information for rivers. Initial comparisons with actual measured water parameters (salinity and suspended solids) indicate that both models exhibit good agreement with the actual values.

Enhancement of microcrystalline identification of gamma-hydroxybutyrate.

An enhancement of the microcrystalline test for the detection of gamma-hydroxybutyrate (GHB) is described. The original test used a silver/copper reagent which consisted of 0.1 g of silver nitrate and 0.1 g of copper nitrate in 10 mL water. The enhanced test utilizes lanthanum nitrate in place of copper nitrate. A detection limit of 0.5 mg/mL was achieved and the visual discrimination was improved because of larger sized crystals. Transient crystals were observed between 0.1 and 0.4 mg/mL. Silver nitrate alone appeared to be suitable for GHB detection but was not specific as other hydroxyl acids, such as glycolic acid, produced a similar crystal pattern. Tests conducted on chemical precursors of GHB and substances with similar biological activity highlight the specificity of the enhanced test. The reagent is therefore selective and sensitive for GHB in aqueous solutions. However, in beverage testing, crystal formation appeared to be inhibited for some drinks. Citric acid was identified as a possible interference depending on its concentration relative to GHB.

Review of analytical techniques for arson residues.

Arson is a serious crime that affects society through cost, property damage, and loss of life. It is important that the methods and technologies applied by fire investigators in detection of evidence and subsequent analyses have a high degree of reliability, sensitivity, and be subject to rigorous quality control and assurance. There have been considerable advances in the field of arson investigation since the 1950s. Classification of ignitable liquids has been updated to include many new categories due to developments in the petroleum industry. Techniques such as steam or vacuum distillation and gas chromatography (GC) with flame ionization detection that may have been considered acceptable--even a benchmark--40 years ago, are nowadays generally disfavored, to the extent that their implementation may almost be considered as ignorance in the field. The advent of readily available mass spectrometric techniques has revolutionized the field of fire debris analysis, increasing the degree of sensitivity and discrimination possible considerably. Multi-dimensional GC--particularly GC x GC--while not yet widely applied, is rapidly gaining recognition as an important technique. This comprehensive review focuses on techniques and practices used in fire investigation, from scene investigation to analysis.

The partitioning of alkylphenolic surfactants and polybrominated diphenyl ether flame retardants in activated sludge batch tests.

Polybrominated diphenyl ethers and nonylphenol polyethoxylates have been reported to be estrogenic and may enter the aquatic environment through the discharge of treated sewage effluent. Therefore, their fate during wastewater treatment processes is an important factor in determining their environmental impact. Batch tests with activated sludge from a Husmann apparatus were used to determine the effects of physico-chemical properties and sludge characteristics on the partitioning of polybrominated diphenyl ether flame retardants and nonylphenol polyethoxylate surfactants during biological wastewater treatment. Hydrophobic compounds, those with high logK(ow) values, were sorbed more rapidly and to a greater extent to the solid phase than more soluble compounds. For these hydrophobic compounds sorption may become an increasingly important removal mechanism as sludge age and therefore solids content increase. The initial rate of partitioning was greatest for the most hydrophobic compounds but all rates diminished with time as a result of progressive saturation of sorbent binding sites, a reduction of sorbate availability and as a consequence of the system reaching equilibrium. The sorption of polybrominated diphenyl ethers fit Freundlich adsorption isotherms demonstrating generally increasing adsorption capacity and efficiency with increasing hydrophobic nature. A correlation between increasing logK(ow) and increasing organic matter content was also observed for both polybrominated diphenyl ethers and nonylphenol polyethoxylates indicating the organic content of mixed liquor will also be influential in removing compounds during wastewater treatment.

Degradation of nonylphenolic surfactants in activated sludge batch tests.

The fate of nonylphenol polyethoxylate surfactants in the activated sludge wastewater treatment process is a concern due to the formation of estrogenic nonlyphenols on degradation and due to the large amounts discharged to the aquatic environment through sewage treatment works. Batch tests using activated sludge from a Husmann apparatus were used to determine the effects of these compounds physico-chemical properties and biological sludge characteristics on biodegradation. Degradation of nonylphenol polyethoxylates with up to 12 ethoxy groups was observed in unacclimated sludge with a concomitant production of nonylphenol and short chain nonylphenol polyethoxylate compounds. Degradation was determined to be a biotic process involving intracellular enzyme activity, which resulted in sludge age being an influential parameter. With increasing sludge age there is an increase in mixed liquor solids concentration in activated sludge which results in greater bacterial numbers and the potential for greater species diversity which therefore increases compound degradation. However, increased degradation of long chain compounds resulted in an accumulation of shorter chain compounds and nonylphenol, which are more resistant to degradation.

An assessment of the bioaccumulation of estrone in Daphnia magna.

The bioaccumulation of estrone by Daphnia magna was determined. Direct uptake via the aqueous medium occurred within the first 16 h. A bioconcentration factor of 228 was established over all temporal periods. Ingestion via Chlorella vulgaris gave a partitioning factor of 24, which may approximate to a biomagnification factor assuming steady state conditions. These preliminary results indicate that the partitioning to Daphnia magna via the food source, C. vulgaris is less significant than bioconcentration.