skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Linking ammonium nitrate‐aluminum ( AN‐AL ) post‐blast residues to pre‐blast explosive materials using isotope ratio and trace elemental analysis for source attribution
Abstract Forensic science practitioners are often called upon to attribute crimes using trace evidence, such as explosive remnants, with the ultimate goal of associating a crime with a suspect or suspects in order to prevent further attacks. The explosive charge is an attractive component for attribution in crimes involving explosives as there are limited pathways for acquisition. However, there is currently no capability to link an explosive charge to its source via post‐blast trace residues using isotope ratios or trace elements. Here, we sought to determine if pre‐blast attribution signatures are preserved after detonation and can be subsequently recovered and detected. A field study was conducted to recover samples of post‐blast explosives from controlled detonations of ammonium nitrate‐aluminum (AN‐Al), which were then analyzed via isotope ratio mass spectrometry (IRMS) and inductively coupled plasma‐mass spectrometry (ICP‐MS) for quantitation and profiling of isotopes ratio and trace element signatures, respectively. Oxygen and nitrogen isotope ratios from AN‐Al yielded some of the most promising results with considerable overlap within one standard deviation of the reference between the spreads of pre‐ and post‐blast data. Trace element results from AN‐Al support the findings in the isotope ratio data, with 26 elements detected in both pre‐ and post‐blast samples, and several elements including B, Cd, Cr, Ni, Sn, V, and Zn showing considerable overlap. These preliminary results provide a proof‐of‐concept for the development of forensic examinations that can attribute signatures from post‐blast debris to signatures in pre‐blast explosive materials for use in future investigations.  more » « less
Award ID(s):
1828492
PAR ID:
10469655
Author(s) / Creator(s):
; ; ; ; ;
Publisher / Repository:
Journal of Forensic Sciences
Date Published:
Journal Name:
Journal of Forensic Sciences
Volume:
68
Issue:
2
ISSN:
0022-1198
Page Range / eLocation ID:
407 to 415
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Isotope ratio analyses of trace elements are applied to tooth enamel, ostrich eggshell, and other archaeological hard tissues to infer mobility and other aspects of hominin and animal paleoecology. It has been assumed that these highly mineralized tissues are resistant to diagenetic alteration, but this is seldom tested and some studies document diagenetic alteration over brief time spans. Here, we build on existing research on Maximum Threshold Concentrations (MTCs) to develop screening tools for diagenesis that can inform heavy isotopic analyses. The premise of the MTC approach is that archaeological tissues are likely contaminated and unsuitable for isotope ratio analysis when they exceed characteristic modern concentration ranges of trace elements. Furthermore, we propose a new metric called the Maximum Threshold Ratio (MTR) of 85Rb/88Sr or whole element Rb/Sr, which can be measured simultaneously with 87Sr/86Sr during laser ablation (LA) MC-ICP-MS or applied during post hoc screening of specimens. We analyzed 56 enamel samples from modern Kenyan mammals and 34 modern ostrich eggshells from South Africa, Namibia, and the United States by solution ICP-MS, as well as a subset of shells using LA-MC-ICP-MS. Our results indicate that thresholds are consistent across taxa at a single location, but likely vary across locations. Therefore, MTCs and MTRs need to be tissue and locality specific, but not necessarily taxon-specific. Other important differences are observed between the inner and outer surfaces of the eggshells and between LA and solution ICP-MS. This exploratory study provides guidelines for building reference thresholds to screen enamel and eggshell for diagenesis potentially impacting biogenic isotope ratios. 
    more » « less
  2. ABSTRACT We report isotope data for C, N, Al, Si, and S of 33 presolar SiC and Si3N4 grains (0.3–1.6 $$\mu$$m) of Type X, C, D, and N from the Murchison CM2 meteorite of likely core-collapse supernova (CCSN) origin which we discuss together with data of six SiC X grains from an earlier study. The isotope data are discussed in the context of hydrogen ingestion supernova (SN) models. We have modified previously used ad-hoc mixing schemes in that we considered (i) heterogeneous H ingestion into the He shell of the pre-SN star, (ii) a variable C-N fractionation for the condensation of SiC grains in the SN ejecta, and (iii) smaller mass units for better fine-tuning. With our modified ad-hoc mixing approach over small scales (0.2–0.4 M⊙), with major contributions from the O-rich O/nova zone, we find remarkably good fits (within a few per cent) for 12C/13C, 26Al/27Al, and 29Si/28Si ratios. The 14N/15N ratio of SiC grains can be well matched if variable C-N fractionation is considered. However, the Si3N4 isotope data point to overproduction of 15N in hydrogen ingestion CCSN models and lower C-N fractionation during SiC condensation than applied here. Our ad-hoc mixing approach based on current CCSN models suggests that the O-rich O/nova zone, which uniquely combines explosive H- and He-burning signatures, is favourable for SiC and Si3N4 formation. The effective range of C/O abundance variations in the He shell triggered by H ingestion events in the massive star progenitor is currently not well constrained and needs further investigation. 
    more » « less
  3. Abstract Fluids mediate the transport of subducted slab material and play a crucial role in the generation of arc magmas. However, the source of subduction-derived fluids remains debated. The Kamchatka arc is an ideal subduction zone to identify the source of fluids because the arc magmas are comparably mafic, their source appears to be essentially free of subducted sediment-derived components, and subducted Hawaii-Emperor Seamount Chain (HESC) is thought to contribute a substantial fluid flux to the Kamchatka magmas. Here we show that Tl isotope ratios are unique tracers of HESC contribution to Kamchatka arc magma sources. In conjunction with trace element ratios and literature data, we trace the progressive dehydration and melting of subducted HESC across the Kamchatka arc. In succession, serpentine (<100 km depth), lawsonite (100–250 km depth) and phengite (>250 km depth) break down and produce fluids that contribute to arc magmatism at the Eastern Volcanic Front (EVF), Central Kamchatka Depression (CKD), and Sredinny Ridge (SR), respectively. However, given the Tl-poor nature of serpentine and lawsonite fluids, simultaneous melting of subducted HESC is required to explain the HESC-like Tl isotope signatures observed in EVF and CKD lavas. In the absence of eclogitic crust melting processes in this region of the Kamchatka arc, we propose that progressive dehydration and melting of a HESC-dominated mélange offers the most compelling interpretation of the combined isotope and trace element data. 
    more » « less
  4. ABSTRACT The trace element composition of planktic foraminifera shells is influenced by both environmental and biological factors (‘vital effects’). As trace elements in individual foraminifera shells are increasingly used as paleoceanographic tools, understanding how trace element ratios vary between individuals, among species, and in response to high frequency environmental variability is of critical importance. Here, we present a three-year plankton tow record (2010–2012) of individual shell trace element (Mg, Sr, Ba, and Mn) to Ca ratios in the planktic species Globigerina ruber (pink), Orbulina universa, and Globorotalia menardii collected throughout the upper 100 m of Cariaco Basin. Plankton tows were paired with in situ measurements of water column chemistry and hydrography. The Mg/Ca ratio reflects different calcification temperatures in all three species when calculated using species-specific temperature relationships from single-species averages of Mg/Ca. However, individual shell Mg/Ca often results in unrealistic temperate estimates. The Sr/Ca ratios are relatively constant among the four species. Ratios of Mn/Ca and Ba/Ca are highest in G. menardii and are not reflective of elemental concentrations in open waters. The Mn/Ca ratio is elevated in all species during upwelling conditions, and a similar trend is demonstrated in Neogloboquadrina incompta shells from the California margin collected during upwelling periods. Together this suggests that elevated shell Mn/Ca may act as a tracer for upwelling of deeper water masses. Our results emphasize the large degree of trace element variability present among and within species living within a limited depth habitat and the roles of biology, calcification environment, and physical mixing in mediating how trace element geochemistry reflects environmental variability in the surface ocean. 
    more » « less
  5. A synthetic laser ruby crystal (HD-LR1) is introduced as a new matrix-matched reference material for secondary ionization mass spectrometry (SIMS) analysis of oxygen isotopes in corundum. Laser fluorination isotope ratio mass spectrometry (LF-IRMS) bulk analyses of multiple mg-sized fragments are homogenous, averaging δ18O = +18.40 ± 0.14‰ (95% confidence interval, n = 23) and Δ′17O = −0.368 ± 0.005‰ (as deviation from slope 0.528 for δ′17O vs. δ′18O at 95% conf., n = 11) relative to Vienna Standard Mean Ocean Water (V-SMOW). SIMS spot analyses show homogeneous O-isotopic values at the ng-scale independent of the location in the HD-LR1 single crystal and in four different crystallographic orientations. However, sample surface topography as an artefact of polishing corundum embedded in epoxy creates excess variability in δ18O within ∼100 μm from the edges of the grains. HD-LR1 is a chemical pure crystal with only Cr as a trace component detected at 276 μg g−1 by EPMA, whereas Be, often introduced in artificial gem enhancement, is <0.002 μg g−1 based on SIMS analyses. Therefore, HD-LR1 can also be used as a reference material for Cr, or as a blank for other trace element analyses of corundum by SIMS or LA-ICP-MS. 
    more » « less