High-quality counterfeit stamp impressions made by inkjet printers remain challenging in questioned document examination and forensic analyses. A dataset comprised of various printed stamp impressions, using ten options of conditions and materials, and hand stamped impressions was generated. In this paper, we report printed impressions in pure color and high-quality printing mode are very similar to hand stamped impressions in terms of their microscopic characteristics. These similarities may lead to incorrect conclusions via traditional identification methods. Here, we proposed a method for identifying counterfeit stamp impressions via texture features and image quality parameters extracted from impressions. First, the statistical analysis methods were used to verify a significant difference between the printed and hand stamped impressions. Principal component analysis (PCA) was used to show the variation between the impressions, and the differences between printed and hand stamped impressions were obvious in the three-dimensional plot. After filtering the background of the stamp impressions, image processing analysis was introduced to extract features of gray level co-occurrence matrix (GLCM), segmentation-based fractal texture analysis (SFTA), local binary pattern (LBP), and image quality metrics (IQM), which were used to characterize the stamp impressions. Finally, specific cases were simulated by random selection, based on the dataset of stamp impressions, and an evaluation system for stamp evidence was established to calculate the likelihood ratios (LRs) under two alternative hypotheses. The likelihood ratio interprets calibrated evaluations on the strength of stamp impressions as evidence. We can also balance these LRs against the rates of misleading evidence with a reasonable performance (equal error rate = 0.048). This paper provides a system to differentiate high-quality printed and hand stamped impressions with reasonable performance.

Over the years, forensic science has primarily positioned itself as a service provider for the criminal justice system, following the dominant and traditional reactive law enforcement model. Unfortunately, this focus has limited its capacity to provide knowledge about crime systems and to support other forms of policing styles through forensic intelligence. Although forensic intelligence research has steadily developed over the last few years, it is rarely covered in the core of academic teaching and research programs. Developing forensic intelligence programs would empower graduates with an awareness of forensic intelligence meaning and models, creating great opportunities to shape their future professional activities and progressively shift the dominant paradigm through a bottom-up approach. In this article, the teaching and learning strategies in forensic intelligence developed at the University of Lausanne (Switzerland) and adapted at the University of Technology Sydney (Australia) and the Université du Québec à Trois-Rivières (Canada) are presented. The objective behind the strategy is to reflect on and work on real case scenarios using a progressive teaching and learning approach that builds upon the theory and practical exercise putting students in real-life situations. Through this innovative learning process, students move away from the Court as the sole end purpose of forensic science. They learn to adopt different roles, adopt a proactive attitude as well as work individually and collaboratively. This teaching and learning strategy breaks the current silos observed in the forensic science discipline by focusing on processes and critical thinking. It can be foreseen, through the evolution of crime and policing models, that the learning and teaching strategy described in this article offers and will offer the students with many new job opportunities. The article concludes with the advantages that such teaching and learning programs in forensic intelligence bring to the forensic science community.

The use of plastics is extremely prevalent in society, with most individuals likely to handle several plastic items per day. It is therefore not surprising that many exhibits recovered from the scene of a crime are plastics, which are processed and examined for traces such as fingermarks. Societal trends have been pushing towards more environmentally friendly products with alternatives to traditional disposable plastics becoming increasingly available. These alternate plastics have different chemical compositions and physical properties, which may impact fingermark development for these substrates. As most detection techniques are known to be substrate-dependent, it is crucial to review current methods and procedures to examine how effective they are on new materials. The aim of this research was to assess a range of fingermark detection techniques on biodegradable plastics and provide recommendations for the preferred technique. First, the prevalence of these materials in the Australian market was evaluated. Over 40 different plastics obtained within the Sydney area were then divided into six broad categories using consumer information in combination with ATR-FTIR spectroscopy analysis. Following this, selected plastics from each category were used as substrates for the fingermark development study. In total, 6480 fingermark specimens were collected as split marks, to form 2160 fingermark comparisons. Each substrate was then developed with four fingermark detection techniques suitable for plastic substrates: cyanoacrylate (CA) fuming, vacuum metal deposition (VMD), powder suspensions (PS), and single metal deposition (SMD). SMD resulted in the most consistent development method across all tested substrates. VMD was able to successfully develop fingermarks on polyethylene-based plastics, but led to poorer results on alternative plastics, while CA fuming and PS were notably more dependent on the surface texture. This research was successful in confirming that biodegradable plastics do in fact have an impact on fingermark development techniques commonly applied on traditional plastics and recommendations have been formed to aid in operational contexts to improve the potential to recover latent fingermarks from biodegradable plastics.

In a field study of insect colonization on domestic pig carcasses, the typical colonization sequence took a different turn midway through decomposition when Necrodes surinamensis (Fabricius) (Coleoptera: Silphidae) dramatically increased in abundance on some carcasses. This provided an opportunity to test the prediction that N. surinamensis would aggregate at clumped carcasses but not as much at dispersed carcasses, thus leaving enough resources in less heavily colonized habitat patches to support weaker competitors, as predicted by the aggregation model of coexistence. Larger aggregations of this silphine beetle resulted in the collapse of blow fly (Diptera: Calliphoridae) maggot populations due to intraguild predation, and a decline or exclusion of late-successional insect species. This phenomenon has been reported in a European Necrodes species but it is the first time it is documented with N. surinamensis, a widespread species in North America. Substantial increases in adult and larval populations of N. surinamensis were first documented on clumped carcasses and were not as pronounced on dispersed carcasses. The specifics of N. surinamensis aggregations are discussed with reference to ecological and forensic implications, including the fact that feeding by N. surinamensis larvae makes the remains appear to have been altered by scavengers and decomposing for longer than they have.

The Death Certificate (DC) is an important medical-legal. However, despite its importance, the professionals involved are not well trained and consequently there exist many errors in completion. This situation can cause misclassification in mortality statistics, but also it means that many natural deaths end up being studied by the medical examiner, entailing a waste of resources. An analysis of 1974 DCs in Madrid is carried out to assess the quality of the completion, discover the main errors in the certificates and analyse possible improvement strategies. The study highlights that the demographic and personal information about the deceased is mostly correct; in 16,2 % of the cases the official document was not used; 91 % of the DCs in the sample have a certain degree of error (major or minor); and 38,4 % of the documents chain of causes were incorrect. The main measure proposed is increased training for certifiers, which should begin with activities at undergraduate level and continue later with periodic training workshops. In addition, we consider it essential to digitalise DCs in Spain. This would greatly facilitate completion. It is also proposed that medical examiners use, in Spain, a document similar to the official DC so that the statistics of violent and natural deaths which have required the medical examiners' intervention will improve.

Since the publication of Lamendin's age estimation technique, the root dentin translucency has received increasing attention as an important indicator of age. Recently, Parra and colleagues presented the Forensic International Dental Database (FIDB), a proposal to estimate age at death in adults based on Bayes theorem by applying the criteria of Lamendin's technique. The present study aims to update the procedure and to evaluate a new version of the method (named FIDBv2) using two control samples from Colombia and Greece. The performance of this new version was acceptable and suggests that the method is suitable for age at death estimation in adult individuals from different forensic contexts. The best approximations to chronological age were obtained for individuals between 30 and 60 years old, with errors less than 10 years. The age estimations calculated on control samples suggest the adequate performance of FIDBv2 on individuals from varied populations. It can be stated that the FIDBv2 constitutes a solid alternative to be used in contexts where no additional data are available. Here we reinforce the initial idea that this model for estimating age at death in adults may be generalizable to any forensic context in the world.

This study expands upon a previously developed method that quantifies the similarity of the compared tape edges by systematically studying the effect of several separation methods and tape grades on the quality of a fit. Analysts examined more than 3300 pairs of hand-torn or scissor-cut duct tapes from three different tape grades while they were kept blind from the ground truth to minimize bias. The samples were examined following a three-step methodology: 1) qualitative assessment of the overall edge alignment and description of edge pattern, 2) macroscopic evaluation of the edges' features, 3) bin by bin subunit assessment of tape edges and estimation of the edge similarity score. A report template was designed to maintain records of the decision-making process. In the second and third steps, eight comparison features were defined and documented using auto-populated cell options. Generally, misidentification rates were low, with no false positives reported. Coinciding with previous research, low scores (under 20%) provided the most support for a non-fit conclusion, while high scores (80% or higher) supported a fit conclusion. A statistical analysis of the separation method and quality of tape revealed a potential interaction between these factors and showed that they significantly impact the edge scores for true fitting pairs, but not the true non-fits' scores. The developed comparison and documentation criteria can assist practitioners with a more straightforward, consistent, and transparent interpretation and reporting approach.

This research explores DNA consistency and attempts to detect STR profiles from the degrading menstrual blood samples (MBS) as reliable forensic evidence. Peripheral (PBS) and MBS of 30 healthy fertile females were taken on the menstrual cycle's second day. They were obtained at different time periods (0, 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 24, and 48 h) at 25 °C. DNA evaluation was fulfilled to analyze DNA profiles. A considerable elevation in the median concentrations of DNA between 0 and 14-h intervals were documented, whereas decreased extents were registered between 16 and 48 h. Moreover, complete STR profiles (24/24) for DNA were discovered in all the intervals (0, 2, and 48 h). Periods of 0-8 h demonstrated the maximum extents of DNA materials. Full STR were discovered in all the intervals (0, 2, and 48 h). Eventually, MBS can be utilized as forensic evidence.

In forensic work, predicting the age of the criminal suspect or victim could provide beneficial clues for investigation. Epigenetic age estimation based on age-correlated DNA methylation has been one of the most widely studied methods of age estimation. However, almost all available epigenetic age prediction models are based on autosomal CpGs, which are only applicable to single-source DNA samples. In this study, we screened the available methylation data sets to identify loci with potential to meet the objectives of this study and then established a male-specific age prediction model based on 2 SNaPshot systems that contain 13 Y-CpGs and the mean absolute deviation (MAD) values were 4-6 years. The multiplex methylation SNaPshot systems and age-predictive model have been validated for sensitivity (the DNA input could be as low as 0.5 ng) and male specificity. They are supposed to have feasibility in forensic practice. In addition, it demonstrated that the method was also applicable to bloodstains, which were commonly found at crime scenes. The results showed good performance (the training set: R2 = 0.9341, MAD = 4.65 years; the test set: R2 = 0.8952, MAD = 5.73 years) in case investigation for predicting male age. For mixtures, when the male to female DNA ratio is 1:1, 1:10, the deviation between the actual age and the predicted age obtained by the model was less than 8 years, which offers great hope for future prediction of the age of males in mixtures and will be a powerful tool for special cases, such as sexual assault. Furthermore, the work provides a basis for the application of Y-CpGs in forensic science.

The synthetic cannabinoid receptor agonist (SCRA) market is undergoing important changes since the enactment of the 2021 class-wide generic SCRA ban in China, one of the most important source countries for new psychoactive substances (NPS). Recently, various compounds with new structural features, synthesized to bypass this legislation, have entered the recreational drug market. Certain monocyclic pyrazole-carrying "FUPPYCA" SCRAs have been sporadically detected since 2015 without gaining further popularity. However, as evidenced by their recent detection in Scottish prisons, 5F-3,5-AB-PFUPPYCA and 3,5-ADB-4en-PFUPPYCA have re-emerged, potentially triggered by the new legislative ban. The aim of this study was to characterize the in vitro intrinsic CB1 and CB2 receptor activation potential of 5F-3,5-AB-PFUPPYCA and 3,5-ADB-4en-PFUPPYCA, as well as 4 analogs (5F-3,5-ADB-PFUPPYCA, 3,5-AB-CHMFUPPYCA, 5,3-AB-CHMFUPPYCA and 5,3-ADB-4en-PFUPPYCA) using live cell β-arrestin 2 recruitment assays. Most analogs were essentially inactive at either CB1 or CB2, with only 3,5-AB-CHMFUPPYCA, 5,3-AB-CHMFUPPYCA and 5,3-ADB-4en-PFUPPYCA showing a limited activation potential at CB1. Furthermore, the importance of the position of the tail structure was demonstrated, with 5,3 regioisomers being more active than their 3,5 analogs. Moreover, all compounds exhibited antagonistic behavior at both receptors, which may be associated with their structural resemblance to cannabinoid antagonists and inverse agonists. Although the 3,5 regioisomers of these "FUPPYCA" SCRAs circumvent the Chinese ban, it is unlikely that these SCRAs will pose a major threat to public health, given the lack of pronounced CB receptor activity.

It is a commonly held belief that drug residues may affect the integrity of DNA and/or interfere with DNA analysis, and therefore DNA on drug paraphernalia and the associated drugs may be overlooked as a source of evidence. This study investigated whether DNA could be isolated from a drug residue-bearing surface to ascertain whether a forensically useful DNA profile could be obtained. Human blood and pre-extracted "naked" DNA were deposited on samples of acetaminophen, codeine, morphine, oxycodone, ketamine, and synthetic cannabinoids and left for an hour before DNA extraction using DNA-IQ™. To investigate DNA integrity, the absolute amount of DNA recovered, degradation index, and number of PCR cycles required for the IPC to reach threshold (Ct), number of reportable alleles and average peak height (APH) in the DNA profile, were examined. The samples were also qualitatively analysed using LC:MS to determine if any residual drugs were present in the samples post-DNA extraction. Overall, the drugs had no to minimal degradation or inhibitory effects on the DNA with sufficient DNA recovered to generate a partial or full DNA profile in 80% of naked DNA samples and 100 % of blood samples. The amount of DNA collected was sufficient for further analysis in 86% of naked DNA samples, and 100% of blood samples, with all median APH values being over the 175 RFU standard. Chemical analysis showed that traces of the drug were still present in the samples after DNA extraction was performed. Therefore, this study demonstrates forensically useful DNA can be recovered from surfaces bearing drug residues, even when sampling directly from the samples of drugs.

Overlapping fingermark images are sometimes discarded because fingermark collation for the individual fingermarks is difficult. Fluorescence hyperspectral data (HSD) measured using the models of double overlapping fingermarks obtained under the excitation of a high-power, continuous wave, green laser is suitable for obtaining individual fingermark images. However, there are limitations such as the problems on each spectrum of the individual fingermark and the forensic value of the obtained images. In this study, independent component analysis (ICA) was applied to the fluorescence HSD obtained from the models of doubly overlapping fingermarks, to obtain independent component (IC) spectra and the corresponding IC images. Forensic value of the obtained IC images was examined, considering the possibility of fingermark collation in masked fashion to the model sample information. The IC images obtained from the HSD had enough potential to enable extracting twelve minutiae required for fingermark collation if the image quality was good.

There appears to be some hesitation within the forensic biology community to formally evaluate and report on findings given activity level propositions. This hesitance in part stems from concerns about the lack of relevant data on the dynamics of biological traces and doubt about the relevance of such expert opinions to the trier of fact. At the Netherlands Forensic Institute formal evaluative opinions on the probability of case findings given propositions at the activity level are provided since 2013, if requested by a mandating authority. In this study we share the results from a retrospective analysis of 74 of such requests. We explore which party initiates requests, the types of cases that are submitted, the sources of data being used to assign probabilities to DNA transfer, persistence, prevalence and recovery (TPPR) events, the conclusions that were drawn by the scientists, and how the conclusions were used by the courts. This retrospective analysis of cases demonstrates that published sources of data are generally available and can be used to address DNA TPPR events in most cases, although significant gaps still remain. The study furthermore shows that reporting on forensic biology findings given activity level propositions has been generally accepted by the district and appeal courts, as well as the other parties in the criminal justice system in the Netherlands.

Sudden cardiac death (SCD) is the leading cause of natural death worldwide which is responsible for almost half of all heart disease deaths, making it a substantial public health problem. Previous epidemiological studies from different countries have demonstrated the significant SCD incident difference rate between males and females. Besides environmental and social effects, differential genetic architecture also underlines the SCD incidence discrepancy. To this end, the functional (CAG)n repeat polymorphism within Androgen Receptor (AR) gene was analyzed to evaluate its associations with SCD originated from coronary artery disease (SCD-CAD) susceptibility in Chinese populations using 182 SCD-CAD cases and 564 healthy controls. At allelic level, the (CAG)26 allele conferred a lower SCD-CAD risk in males (adjusted odds ratio [OR] = 0.428; 95% confidence interval [CI] = 0.254, 0.915; P = 0.023). On the contrary, the (CAG)26 allele was reversely associated with a higher SCD-CAD risk in females (OR = 2.581; 95% CI = 0.944, 7.056; P = 0.057). Further cutoff strategy analysis revealed that those male subjects carrying shorter allele (≤26 repeats) had significantly lower SCD-CAD risk (OR = 0.343; 95% CI = 0.221, 0.531; P = 8.1653e-7). Additionally, an allele-dependent SCD risk tendency was observed in male subjects. Specifically, compared with males carrying allele longer than 26 repeats, the SCD-CAD risk (OR value) for male subjects carrying shorter alleles (from 25 to 21) gradually increased from 0.437 to 0.533, indicating the (CAG)26 allele of the repeat polymorphism may be the watershed in male SCD etiology. Lastly, the length variations associated with multiple phenotypes were also summarized. Collectively, our results revealed for the first time that the (CAG)n repeat polymorphism within the AR gene was associated with SCD-CAD risk in Chinese populations with sex discrepancy, proposing a new candidate genetic marker for molecular diagnosis of SCD-CAD. Furthermore, a sex-dependent SCD-CAD risk stratification and prevention approach was encouraged. Further studies with more female samples were warranted to validate our findings.

In this study, glass from 30 different portable electronic devices (PED) screens, 15 screen protectors (SP), and 3 brands of liquid glass (LG) were analyzed using a µ-XRF instrument equipped with two silicon drift detectors (SDD). Additional analysis of six fragments, all originating from the same PED and SP screen, assessed the elemental homogeneity within a single glass source. Examinations of the 30 PEDs and the majority of the SP screens revealed spectra with low sodium and high potassium, which is likely due to the ion exchange process at the surface during the glass manufacturing process. The absence of calcium in the XRF spectra was also characteristic of PED formulations. Initial spectral overlay examinations classified the PED and SP samples into major groups based on their distinctive elemental profiles (5 PED groups, 4 SP groups). Further discrimination of within-group samples was possible when considering reproducible differences in signal intensities (discrimination 98.4 % PED, 98.1 % SP). Additionally, a 3 s (3 % Relative Standard Deviation, RSD) comparison criterion produced the lowest false exclusion rates among same-source fragments (3.3 % PED, 0.8 % SP) while maintaining a high discrimination power among different-source fragments (98.4 % PED, 100 % SP). Same source PED and SP samples resulted in low variability within most elements examined (< 8 % RSD), except for potassium. An experimental threshold established from the quantitative metric of spectral similarity, spectral contrast angle (SCA) ratio of same-source and different-source datasets, produced false exclusion and false inclusion rates of 4 % or 0.95 % for PED and SP fragments, respectively. Spectra of just the liquid glass residues indicated some major elements present but the effect of these elements in PED fragments treated with liquid glass was not significant. This study provides a preliminary understanding of the elemental composition of modern PED glasses and their accessories and the discrimination capability of µ-XRF for forensic comparisons.

An in-depth study into the physical substrate characteristics such as substrate surface roughness, topography, and physicochemical characteristics like wettability and surface free energy (SFE) was conducted to investigate the impact on the deposition and adherence of touch and salivary deposits on aluminium and polypropylene. A robust protocol was established to generate a set of substrates with a controlled linear surface roughness range (0.5-3.5 µm) in order to identify the impact of surface roughness on DNA transfer, persistence, prevalence, and recovery (DNA-TPPR). The polypropylene substrate was shown to produce fibres when artificially roughened, becoming more prominent at a higher surface roughness range, and has shown to have a direct impact on the distribution of salivary and touch deposits. At the low to moderate surface roughness range 0.5-2.0 µm, salivary and touch deposits have generally shown to follow the topographical features of the substrate they were deposited on, before a plateau of the surface roughness measure on the deposit was observed, indicating that a saturation point was reached and the grooves in the substrate were beginning to fill. Touch deposits have shown to maintain a consistent deposition height pre-surface roughness threshold, irrespective of substrate surface roughness while the deposition height of salivary deposits was heavily influenced by substrate surface roughness and topography. The substrate SFE, wettability, hydrophobicity, and the surface tension of the deposit was shown to drive the adhesion properties of the saliva and touch deposits on the respective substrates, and it was observed that this may be of importance for the improvement of the current DNA-TPPR understanding, DNA sampling protocols, and DNA transfer considerations within casework.

In the pattern comparison disciplines, forensic practitioners evaluate two impressions with respect to the same-source and different-sources propositions. The results are communicated using a pre-determined conclusion scale, and in the friction ridge discipline Identification is typically the highest category on the scale for reporting evidence supporting the same source proposition. Although error rates have been measured in most disciplines, there are no widespread quantitative approaches and therefore most conclusions rely on subjective human evaluations. The current work uses articulation decisions provided by fingerprint examiners in error rate studies to produce a quantitative likelihood ratio measure that characterizes the strength of the support for the two propositions. We use an ordered probit model to summarize the distribution of responses of examiners who participated in error rate and validation studies. We then aggregate the data for all image pairs in a database to construct a set of likelihood ratios based on the ratio of the two strength-of-support values. We find that these values are modest relative to values typically produced by DNA analysis or implied by current fingerprint articulation language. The technique can be applied to any pattern comparison discipline for which error-rate data is available, and therefore can be used to appropriately weigh the evidence from different disciplines.

The ability to determine the post-mortem interval (PMI) in complex death investigations involving human remains, is a vital task faced by law enforcement. Establishing the PMI in a case can significantly aid in the reconstruction of forensically relevant events surrounding that death. However, due to the complexities surrounding the decomposition of human remains, the determination of the PMI still remains a challenge in some cases. Thus, the identification of biomarkers of human decomposition are an emerging, and essential, area of research. Previous studies have also demonstrated great success in the use of textiles as a host to indirectly capture decomposition by-products. This study reports the successful adaptation and optimisation of an analytical chemical workflow for the targeted analysis of lipids from textiles associated with decomposing human remains using gas-chromatography (GC) coupled with tandem mass spectrometry (MS/MS). This study discusses novel information regarding the complex challenges of matrix effects observed with decomposition samples. In addition, the first lipid profiles obtained from textiles associated with two decomposing human donors from the Australian Facility for Taphonomic Experimental Research (AFTER) using GC-MS/MS are presented.

Hair evidence collected during a forensic investigation has the potential to provide valuable sourcing information through DNA analysis of its root. Over time, hair examiners at the North Carolina State Crime Laboratory observed hair roots being sent for DNA analysis were not yielding profiles as expected. Recent advancements in the Forensic Biology Section's detection limits prompted research into whether changes to the current root removal protocol could increase the likelihood of developing a DNA profile from a hair root. An internal validation was completed for the method of Hematoxylin staining to screen telogen roots for DNA analysis. Over 900 head hairs from approximately 15 living donors were examined for telogen roots. Those roots were stained using Hematoxylin and examined for nuclei. The roots were separated into groups based on nuclei present: Group I (1-10 nuclei), Group II (11-20 nuclei), Group III (21-30 nuclei), Group IV (31-40 nuclei), and Group V (41 or greater nuclei). A set of 64 roots, including a Negative Control (0 nuclei) and a Positive Control (anagen or catagen roots), were sent for quantitative DNA analysis. The data showed a clear separation between Groups I and II, where 36% of Group I verses 80% of Group II passed the quantification cutoff. All samples in the Negative Control, Group I, and the Positive Control were then amplified along with a representative sample in Groups II through V. After amplification, the delineation between Groups I and II maintained with 27% of Group I verses 89% of Group II obtaining DNA profiles. As a result, the nuclei required to obtain a potential DNA profile at our laboratory is eleven or more. Prior to Hematoxylin, anagen, catagen, or telogen roots with follicular tissue were sent for DNA analysis, resulting in 32% of roots yielding DNA results. Following implementation of Hematoxylin into casework in March 2019, the success rate has more than doubled to 69%, illustrating the utility of Hematoxylin root staining in improving casework efficiency. Through this methodology, only roots with the best potential to develop a DNA profile are sent for testing, thereby decreasing DNA caseload, cost, and time of analysis. In fact, Hematoxylin staining has resulted in a 14% reduction in the number of hair roots forwarded for DNA analysis, meaning hairs not meeting nuclear threshold are preserved for future examinations.

Homicide, particularly where a body has been concealed, is uniquely challenging for investigators to estimate the time of occurrence due to the methods employed by perpetrators to hide the body or its constituent parts from detection. The regularity of necrophagous insect lifecycles to determine minimum post-mortem interval (minPMI) is widely employed but remains an unreliable technique if used without a clear understanding of the factors that affect insect access and oviposition behaviour to concealed remains. The purpose of this study was to investigate the effect of wrapping body parts on fly colonisation and implications for minPMI calculations. Field studies were carried out using four treatments of pork (as surrogate body parts), in five replicates, one unwrapped, the other three wrapped in either a black plastic sack, a small-zipped wash bag (to simulate a suitcase), or a plastic sack further placed in a wash bag. Over a 48-h period all the methods of wrapping significantly disrupted the host-finding process of blowflies to dismembered carcasses, with a delay of initial contact and oviposition of 30+h (dependant on wrapping) and even more in wet conditions (48+ h). Egg numbers were also reduced by as much as 99.1% on wrapped samples compared to unwrapped. These new findings highlight the importance of applying adjustments to minPMI calculations when encountering wrapped remains. Advances in the accuracy of minPMI calculations will prevent the waste of valuable police time and resources and better focus the search for witnesses and suspects in homicide investigations.

The use of non-destructive forensic methods for cocaine identification is of outstanding importance, given the amount of samples seized. Techniques such as ATR-FTIR, Raman, and NIR spectroscopy have become alternatives to circumvent this problem, as they allow fast, cheap analysis, and enable the reanalysis of samples. When combined with chemometrics, these spectroscopic methods can be used to determine and quantify cocaine samples, meaning that the limitations of existing techniques can be overcome. This review article covers spectroscopic techniques for identifying cocaine in different forms and matrices, such as food and textiles, which are materials used for smuggling. The chemometric identification of cocaine in oral fluid and water is also discussed. In addition, vibrational spectroscopy techniques using portable equipment are described. This work seeks to evaluate the main chemometric applications of spectroscopic data and to find new perspectives on the identification of cocaine using chemometrics.

Kinship testing using genetic markers such as short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs) is crucial for forensic analysis. Although STR markers have superior discriminatory power due to their highly polymorphic properties, they have several weak points in determining extended distant or complex relationships because of high mutation rates and low success rates in degraded samples. Therefore, SNPs are regarded as promising tools in forensic science because they have low mutation rates and small amplicon sizes. Herein, we propose an SNP panel consisting of 1400 autosomal SNPs obtained from the Korean National Standard Reference Variome (KoVariome) database. To evaluate its performance, in-silico analysis was performed using whole-genome sequencing (WGS) data from 21 Korean families. Subsequently, to estimate pairwise relatedness, kinship coefficients were calculated using PLINK, and Welch's one-way ANOVA test with Games-Howell's pairwise comparison test was performed. As a result, the average kinship coefficients of first- (parent-offspring and full siblings), second- (grandparent-grandchildren and aunt/uncle-niece/nephew), and third- (first cousin and grandniece/grandnephew) degree relatives, and unrelated were 0.24, 0.11, - 0.054, and - 0.0082, respectively. Consequently, relatives (first and second degree) were distinguished from non-relatives; however, further studies are required to investigate more effective SNP markers for discriminating extended kinship. Nevertheless, the results of this study go beyond the scope of screening using the discovered 1400 SNPs in Korean families and suggest the applicability of kinship analysis in the Korean population.

Determining fetal death causes is a complex problem for the forensic pathologist. Beyond the medico-legal context, the expert must be able to evaluate the viability of the fetus at the time of death, to eliminate in-utero fetal death and to determine if the death is related to a fetal, a maternal, a placental cause, or simply related to obstetrical complications. The authors present the case of a 21-year-old woman who unexpectedly gave birth to a fetus during a party. As pregnancy was not acknowledged by the mother (regular menstrual cycles and use of hormonal contraception), no obstetrical check-up had been performed. She would have presented violent abdominal pain and expelled a mass in the toilet. The fetus body, enclosed in the amniotic pouch, and the placenta were found in the toilet. A forensic autopsy was performed jointly by a forensic pathologist and a specialist in fetal pathology. Histological, toxicological and genetic samples were collected. Body morphometry and bone maturation indicated a gestational age of 31-32 weeks of amenorrhea. A significant asphyxia syndrome and non-specific multi-visceral congestion were noted at autopsy. Histological analysis of the fetal tissues revealed a lung and skeletal muscle maturation in accordance with the estimated term. At the brain level, there were signs of anoxia and abnormal cortical development with periventricular nodular heterotopia areas. The placenta microscopic analysis revealed acute chorioamniotitis, the probable cause of the premature fetal expulsion. Toxicological analyses revealed the presence of ecstasy (48 ng/mL) and its metabolite MDA (2 ng/mL) in fetal blood. Although negative in blood, THC-COOH tested positive in urine (9 ng/mL). The fetus was repetitively exposed to cannabis, as Δ9-THC tested positive in hair (51 pg/mg). Maternal hair analysis on 4 × 3 cm evidenced a long-term use of cannabis, while results support single massive exposure to ecstasy. In this article, the authors try to explain the reflexive pathway carried out to establish death causes and the maternal toxic consumption imputability on the cerebral malformations and fetal death. This case illustrates both the interest of toxicological analyses in cases of fetal death and the importance of a collaborative work between forensic and fetal pathologists and toxicologists, which appeared critical to answer in the best conditions to the magistrates questions, as well as to the bereaved families.

Members of the genus Aconitum have been used for millennia, both as poisons and medicines, in Eastern culture. Higenamine has non-selective beta-agonist effects, activating both β1 and β2 adrenoreceptors, and is present in a variety of plants. The World Anti-Doping Agency has banned Higenamine both in competition and out of competition. Due to the common uses of higenamine in Brazilian culture, both as medicine and food, we studied the urinary concentrations of higenamine after the consumption of fruits of the Annona genus. We evaluated whether the ingestion of these fruits has the potential to cause anti-doping code violations. We measured higenamine concentrations for a 72 h period in the urine of ten healthy, physically active males (age 20-30; weight 70-80 kg; not consuming supplements or medications) after eating a unique meal containing fruits. Fruit consumption ranges were: Carica papaya (control) 348 ± 98 g; A. muricata 450 ± 282 g; and A. squamosa 314 ± 60 g. (all mean± SD). Higenamine was measured using ultra-performance liquid chromatography coupled with electrospray-tandem mass spectrometry. The appearance of urinary higenamine occurred within the first 12 h after eating A. muricata (n = 3), and the maximum concentration found was 1.9 ng/mL. The ingestion of A. squamosa has also been shown to cause higenamine urinary excretion. The elimination kinetics of the subjects who ingested A. squamosa (n = 4) were different from each other. After ingestion of the control fruit, C. papaya, we detected no higenamine in the urine of any participants (n = 3). Although the kinetics varied by individuals and fruits, A. muricata ingestion produced higher higenamine excretion; however, the A. squamosa portion weighed ∼66 % of the A. muricata portion. We conclude that eating Annonaceae family fruits cause detectable higenamine excretion. Conversely, single ingestion did not reach the WADA's threshold to cause adverse analytical findings.

A case of fatal left iliac penetrating wound in a thirty-year-old man, during a fight, was presented. The medical file described a transfixing five-centimeter large wound on the left iliac vein and a puncture wound on the left iliac artery. After performing an autopsy, we concluded that the death was secondary to multivisceral failure, secondary to hemorrhagic shock. The judge investigating the case requested a detailed forensic medical reconstructive opinion focusing on the sequence of events leading to the fatal blow. Our having access to the videorecording and the photographs of the crime scene, added to the testimonies of witnesses proved to be a great help to the investigation. The data from the crime scene video recordings allowed us to estimate the victim's physical activity after the fatal stabbing (running between 20 and 140 meters) and the time when he collapsed (between 32s and 1 min) after the stabbing which is rarely described with methods using Closed-Circuit Television material, especially in cases of fatal vascular injuries. Those data are usually estimated from eyewitnesses' accounts, which remain an unreliable method.

Nowadays, the diagnostic value of postmortem microbiological investigations is still a debated topic, but postmortem microbiology (PMM) remains a discipline with great forensic potential. To evaluate the usefulness and diagnostic-forensic value of postmortem microbiological cultures, it has been conducted a study on cadaveric material sampled during autopsy aiming to identify the correct cause of death. The study analyzed 45 cadavers subjected to judicial autopsy, divided into two groups based on the presence or absence of external or internal macroscopic autopsy signs suggesting infectious pathology. In the same cases, both the microbiological and conventional histological investigations have been simultaneously carried out. From the investigations, mono-bacterial, mono-fungal, mixed and negative cultures were observed. In mono-species microbiological growth, the histological epicrisis confirmed an infectious cause of death due to the presence of signs of acute infection with an aggressive infectious agent. In cases where growth was mixed, it was possible to distinguish between simple postmortal contamination and perimortem colonization. Finally, in some cases where the microbiology was negative, this has been essential in highlighting signs of a vital reaction to viral or parasitic infection. The joint and integrated evaluation of the laboratory results made it possible to correctly understand even those peculiar situations in which the PMM results alone would not have been significant. These methods, when combined, constitute an optimal forensic approach for the identification of the real cause of death and thus reduce the number of unsolved cases.

The volume of blood leaked from blood vessels may change due to evaporation of water under the natural influence of the external environment. Bloodstains and dried blood spots (DBS), which describes blood dried in the external environment, are similar in their production and their metabolite quantification profiles. In both bloodstain metabolite analysis in the forensic science field and DBS metabolite analysis in the clinical field, it is important to determine the volume of the origin blood as this affects metabolite quantification results. Therefore, the purpose of this study is to discover the internal standard metabolites that have quantitatively proportional relationships with origin blood volume and maintain constant concentrations even as the age of the bloodstain increases. As a result, the concentrations of L-isoleucine and L-phenylalanine increased in proportion to the origin blood volume of the bloodstain. The differences in concentration of L-isoleucine were significant in all volume comparisons except in the comparison between 65 μL and 85 μL. The differences in concentration of L-phenylalanine were significant in all volume comparisons except between 65 μL and 45 μL and between 65 μL and 85 μL. In addition, it was confirmed that both metabolites tended to maintain constant concentrations without being affected by bloodstain age as the volume became smaller. These internal standard metabolites can be used for estimating the origin blood volume of bloodstains during metabolite analysis of bloodstains and DBS and could provide a volume criterion for standardization when comparing metabolite quantification between samples.

Bayesian Belief Networks (BBNs) can be applied to solve inverse problems such as the post-mortem interval (PMI) by a simple and logical graphical representation of conditional dependencies between multiple taphonomic variables and the observable decomposition effect. This study is the first cross-comparison retrospective study of human decomposition across three different geographical regions. To assess the effect of the most influential taphonomic variables on the decomposition rate (as measured by the Total Decomposition Score (TDS)), decomposition data was examined from the Forensic Anthropology Research Facility at the University of Tennessee (n = 312), the Allegheny County Office of the Medical Examiner in Pittsburgh, US (n = 250), and the Crime Scene Investigation department at Southwest Forensics in the UK (n = 81). Two different BBNs for PMI estimations were created from the US and the UK training data. Sensitivity analysis was performed to identify the most influential parameters of TDS variance, with weaker variables (e.g., age, sex, clothing) being excluded during model refinement. The accuracy of the BBNs was then compared by additional validation cases: US (n = 28) and UK (n = 10). Both models conferred predictive power of the PMI and accounted for the unique combination of taphonomic variables affecting decomposition. Both models had a mean posterior probability of 86% (US) and 81% (UK) in favor of the experimental hypothesis (that the PMI was on, or less than, the prior last known alive date). Neither the US nor the UK datasets represented any cases below 'moderate' support for the value of PMI evidence. By applying coherent probabilistic reasoning to PMI estimations, one logical solution is provided to model the complexities of human decomposition that can quantify the combined effect of several uncertainties surrounding the PMI estimation. This approach communicates the PMI with an associated degree of confidence and provides predictive power on unknown PMI cases.