Dissertations / Theses on the topic 'Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS)'

The need for elemental analysis of biological matrices such as bone, teeth, and plant matter for sourcing purposes has emerged within the forensic and geochemical laboratories. Trace elemental analyses for the comparison of aterials such as glass by inductively coupled plasma mass spectrometry (ICP-MS) and laser ablation ICP-MS has been shown to offer a high degree of discrimination between different manufacturing sources. Unit resolution ICP-MS instruments may suffer from some polyatomic interferences including 40Ar16O+, 40Ar16O1H+, and 40Ca16O+ that affect iron measurement at trace levels. Iron is an important element in the analysis of glass and also of interest for the analysis of several biological matrices. A comparison of the nalytical performance of two different ICP-MS systems for iron analysis in glass for determining the method detection limits (MDLs), accuracy, and precision of the measurement is presented. Acid digestion and laser ablation methods are also compared. Iron polyatomic interferences were reduced or resolved by using dynamic reaction cell and high resolution ICP-MS. MDLs as low as 0.03 ìg g-1 and 0.14 ìg g-1 for laser ablation and solution based analyses respectively were achieved. The use of helium as a carrier gas demonstrated improvement in the detection limits of both iron isotopes (56Fe and 57Fe) in medium resolution for the HR-ICP-MS and with a dynamic reaction cell (DRC) coupled to a quadrupole ICP-MS system. The development and application of robust analytical methods for the quantification of trace elements in biological matrices has lead to a better understanding of the potential utility of these measurements in forensic chemical analyses. Standard reference materials (SRMs) were used in the development of an analytical method using HR-ICP-MS and LA-HR-ICP-MS that was subsequently applied on the analysis of real samples. Bone, teeth and ashed marijuana samples were analyzed with the developed method. Elemental analysis of bone samples from 12 different individuals provided discrimination between individuals, when femur and humerus bones were considered separately. Discrimination of 14 teeth samples based on elemental composition was achieved with the exception of one case where samples from the same individual were not associated with each other. The discrimination of 49 different ashed plant (cannabis)samples was achieved using the developed method.

As a consequence of the widespread use of computers coupled to high-quality printers and different types of papers, forgery, counterfeiting, change of wills, anonymous letter writing and felonious use of the documents have become serious problems. Forensic analysts are always seeking methods that can provide reliable information on whether a specimen collected at the crime scene is linked to the crime or to a source of known origin. Sensitive methods that can provide more detailed characterization of natural or man-made materials or even provide information not previously available to forensic examiners. Recent advances in rapid solid sampling of materials using laser ablation (LA) coupled to inductively coupled plasma mass spectroscopy (ICP-MS) have led to this analytical method to be regarded as the “gold standard” in the field of elemental analysis for trace level components in solids. Another, emerging, analytical technique that uses the same laser pulse to generate a plasma that can be interrogated with spectroscopy is laser induced break down spectroscopy (LIBS). The analysis of ink and paper is also possible because of the surface removal effect of laser interactions with the samples. In the present study, printing inks were analyzed using LIBS, LA-ICP-MS and both of them in tandem mode. In the tandem setup, the light generated during the relaxation of the excited species (LIBS) was used to create a spectral signature of the elements, and the mass-to-charge ratio of the ejected particles (ICP-MS) was used to create a mass spectrum. For a set of 319 printing ink samples, LA-ICP-MS alone provided discrimination greater than 99%. A subset of 43 printing inks, having a very similar elemental profile, was analyzed by tandem LIBS/LA-ICP-MS. The fusion of LIBS and LA-ICP-MS provided additional discrimination through the detection of elements like Ca, Si, Fe, and K by LIBS, that are difficult to detect and confirm using standalone ICP-MS because of the spectral interferences (isobaric and polyatomic) involved. The combination of these two sensors was found to minimize the individual limitations and provide a more complete and representative chemical characterization of printing inks.

Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS) is now a well established analytical technique used to sample solid materials and determine their elemental composition. Two areas that are becoming increasingly important, and for which LA-ICP-MS is a key tool, are bio-imaging and the analysis of micro-particulates. However, current instrumental designs limit the practicality of the technique for these applications. This study investigates the development of a high speed, high efficiency LA-ICP-MS interface through modelling of the flow dynamics of a newly designed laser ablation cell and experimental investigation of single laser pulse response. Through this work the Sniffer-Dual Concentric Injector interface was realised. This interface reduced particle residence times within the laser cell and transport tubing. The interface was also used to investigate turbulence related aerosol dispersion within the ICP and potential designs to overcome this. The resulting design yields an interface with improved sensitivity and reduced aerosol dispersion such that a lower limit of detection is achieved, important when considering the mass of analyte in a single cell or micro-particulate, compared to existing designs. Thus the interface can be used to improve image spatial resolution as the ablation spot size, and thus pixel information, can be reduced; and also reduces total analysis time. The calibration technique Laser Ablation of a Sample In Liquid (LASIL) was also investigated as a means of calibration for solid samples. The investigation lead to the development of LASIL in a droplet, a technique that can be used to calibrate solid samples when a matrix matched standard is unavailable. The mechanism of the technique resulted in an improved laser-energy sample coupling efficiency and a reduction in the liquid to ablated mass ratio, thus decreasing sampling time. As the technique captures the ablated particulate in solution, post chemistry techniques can be used to remove analyte interferences.

Laser Ablation Inductively coupled plasma mass spectrometry (LA-ICP-MS) and Raman spectroscopy are both powerful imaging techniques. Their applications are numerous and extremely potential in the field of biology. In order to improve upon LA-ICP-MS an in-house built cold cell was developed and its effectiveness studied by imaging Brassica napus seeds. To further apply LA-ICP-MS and Raman imaging to the field of entomology a prong gilled mayfly (Ephemeroptera: Leptophlebiidae) from the Róbalo River, located on Navarino Island in Chile, was studied. Analysis of both samples showcased LA-ICP-MS and Raman spectroscopy as effective instruments for imaging trace elements and larger molecules in biological samples respectively.

Cellular therapy is emerging as a clinically viable strategy in the field of solid organ transplantation, where it is expected to reduce the dependency on conventional immunosuppression. This has produced a demand for highly sensitive methods to monitor the persistence and tissue distribution of administered cells in vivo. However, tracking cells presents significant challenges. In many cases transplanted cells are autologous with the immune system of the transplant recipient, and hence are invisible to typical methods of detection. To enable their differentiation, the cells must be labelled with a suitable, non-toxic and long lifetime label, prior to their administration to patients. In addition, administered cells represent only a small fraction of the recipient's endogenous cells, which necessitates the use of an extremely sensitive detection method. Laser ablation – inductively coupled plasma – mass spectrometry (LA-ICP-MS) is an exquisitely sensitive analytical technique, capable of imaging trace elements in complex samples, at high spatial resolution.

The necessity of elemental analysis techniques to solve forensic problems continues to expand as the samples collected from crime scenes grow in complexity. Laser ablation ICP-MS (LA-ICP-MS) has been shown to provide a high degree of discrimination between samples that originate from different sources. In the first part of this research, two laser ablation ICP-MS systems were compared, one using a nanosecond laser and another a femtosecond laser source for the forensic analysis of glass. The results showed that femtosecond LA-ICP-MS did not provide significant improvements in terms of accuracy, precision and discrimination, however femtosecond LA-ICP-MS did provide lower detection limits. In addition, it was determined that even for femtosecond LA-ICP-MS an internal standard should be utilized to obtain accurate analytical results for glass analyses. In the second part, a method using laser induced breakdown spectroscopy (LIBS) for the forensic analysis of glass was shown to provide excellent discrimination for a glass set consisting of 41 automotive fragments. The discrimination power was compared to two of the leading elemental analysis techniques, µXRF and LA-ICP-MS, and the results were similar; all methods generated >99% discrimination and the pairs found indistinguishable were similar. An extensive data analysis approach for LIBS glass analyses was developed to minimize Type I and II errors en route to a recommendation of 10 ratios to be used for glass comparisons. Finally, a LA-ICP-MS method for the qualitative analysis and discrimination of gel ink sources was developed and tested for a set of ink samples. In the first discrimination study, qualitative analysis was used to obtain 95.6% discrimination for a blind study consisting of 45 black gel ink samples provided by the United States Secret Service. A 0.4% false exclusion (Type I) error rate and a 3.9% false inclusion (Type II) error rate was obtained for this discrimination study. In the second discrimination study, 99% discrimination power was achieved for a black gel ink pen set consisting of 24 self collected samples. The two pairs found to be indistinguishable came from the same source of origin (the same manufacturer and type of pen purchased in different locations). It was also found that gel ink from the same pen, regardless of the age, was indistinguishable as were gel ink pens (four pens) originating from the same pack.

[Truncated abstract] The sale of fraudulent South-East Asian ceramics constitutes a large proportion of the illegal artefact and antique trade and threatens to undermine the legitimate international market. The sophistication and skill of forgers has reached a level where, using traditional appraisal by eye and hand, even the most experienced specialist is often unable to distinguish between a genuine and fraudulent piece. In addition, the current scientific method of authentication used by the international antiques and art industry, thermoluminescence (TL) dating, carries severe limitations. The technique has an error margin of +/-20 % and requires the removal of a significant piece of the sample being tested, which decreases both the monetary and cultural value of the artefact. Of more concern, forgers have developed methods which produce false test results and which appear to corroborate false claims for the age of artefacts. Consequently, the use of TL dating for authentication of ancient ceramics, especially those of South-East Asian origin, has now come into serious question. The most suitable method for authenticating ceramics is through provenance establishment. Studies published in the literature have investigated the application of various analytical techniques to provide this information for ceramic wares and have highlighted their potential to be used for provenance establishment. However, the value of each of these techniques is limited rendering them generally unsuitable for practical use in the international antiques and art world to authenticate high-value South-East Asian artefacts. Consequently, there is a desperate need for the development of a robust, accurate and non-destructive method which can be practically applied in the industry to authenticate South-East Asian ceramics. ... Minor variations between spectral profiles of artefacts produced in the same country have also been used to further provenance artefacts to a specific production region or kiln site. The results of analyses have been compiled to form a unique reference database which can be added to in the future and used by experts internationally. Adaptation of the developed sampling and analytical methodologies to allow in-situ sampling of large artefacts using the

The elemental analysis of soil is useful in forensic and environmental sciences. Methods were developed and optimized for two laser-based multi-element analysis techniques: laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) and laser-induced breakdown spectroscopy (LIBS). This work represents the first use of a 266 nm laser for forensic soil analysis by LIBS. Sample preparation methods were developed and optimized for a variety of sample types, including pellets for large bulk soil specimens (470 mg) and sediment-laden filters (47 mg), and tape-mounting for small transfer evidence specimens (10 mg). Analytical performance for sediment filter pellets and tape-mounted soils was similar to that achieved with bulk pellets. An inter-laboratory comparison exercise was designed to evaluate the performance of the LA-ICP-MS and LIBS methods, as well as for micro X-ray fluorescence (μXRF), across multiple laboratories. Limits of detection (LODs) were 0.01-23 ppm for LA-ICP-MS, 0.25-574 ppm for LIBS, 16-4400 ppm for µXRF, and well below the levels normally seen in soils. Good intra-laboratory precision (≤ 6 % relative standard deviation (RSD) for LA-ICP-MS; ≤ 8 % for µXRF; ≤ 17 % for LIBS) and inter-laboratory precision (≤ 19 % for LA-ICP-MS; ≤ 25 % for µXRF) were achieved for most elements, which is encouraging for a first inter-laboratory exercise. While LIBS generally has higher LODs and RSDs than LA-ICP-MS, both were capable of generating good quality multi-element data sufficient for discrimination purposes. Multivariate methods using principal components analysis (PCA) and linear discriminant analysis (LDA) were developed for discriminations of soils from different sources. Specimens from different sites that were indistinguishable by color alone were discriminated by elemental analysis. Correct classification rates of 94.5 % or better were achieved in a simulated forensic discrimination of three similar sites for both LIBS and LA-ICP-MS. Results for tape-mounted specimens were nearly identical to those achieved with pellets. Methods were tested on soils from USA, Canada and Tanzania. Within-site heterogeneity was site-specific. Elemental differences were greatest for specimens separated by large distances, even within the same lithology. Elemental profiles can be used to discriminate soils from different locations and narrow down locations even when mineralogy is similar.

Bei der Schwefelquantifizierung in Kupfer und anderen reinen Metallen zeigte sich in der Vergangenheit eine mangelnde SI-Rückführung und zusätzlich inkonsistente Ergebnisse, wenn verschiedene Methoden verglichen wurden. Um diesen Mangel zu beheben ist ein Referenzverfahren erforderlich, welches SI-rückführbare Werte mit einem zuverlässigen Unsicherheitsbudget ermöglicht. In dieser Studie wurde ein entsprechendes Referenzverfahren zur Quantifizierung von Gesamtschwefel in Kupfer basierend auf der induktiv gekoppelten Plasma-Massenspektrometrie und der Isotopenverdünnungsanalyse (ICP-IDMS) entwickelt. Um diese Probleme zu lösen wurde mit Hilfe der Ionenaustauschchromatographie ein Schwefel-Matrix-Trennverfahren entwickelt. Dieses Trennverfahren wurde mit ICP-IDMS kombiniert, um Schwierigkeiten mit der Kalibrierung zu lösen und fehlende metrologische Konzepte einzuführen. So wurden die in diesem Projekt erzielten IDMS-Messwerte für die Kalibrierung von GDMS und LA-ICP-MS verwendet, beides Verfahren die im industriellen Einsatz üblich sind. Dadurch konnten mit beiden Routineverfahren zuverlässige Ergebnisse erzeilt warden, die zudem auf SI rückführbar sind. Darüber hinaus wurde ein auf der LA-ICP-IDMS basierendes Verfahren entwickelt, um den Probenvorbereitungsschritt von ICP-IDMS mit Schwefel-Matrix-Trennung zu reduzieren. Die Vorteile dieser Methode sind ein geringerer Arbeits- und Zeitaufwand, die SI- Rückführung der Messergebnisse und eine für LA-ICP-MS vergleichsweise hohe Genauigkeit. Die Schlüsselrolle hierbei spielte der innovative Einsatz von Polyethylenfritten als Trägermaterial der aufgelösten Probe. Dadurch war die Quantifizierung von Schwefel in Kupferproben mittels LA-ICP-IDMS möglich. Die wesentlichen Parameter wie Absorptionseffizienz der Fritten und Matrixeffekt wurden untersucht. Das entwickelte Verfahren konnte mit Hilfe der ICP-IDMS vollständig validiert werden.
Sulphur quantification in copper and other pure metals in the past revealed a lack of SI-traceability and also showed inconsistent results, when different methods are compared. Therefore, a reference procedure is required to enable SI-traceable measurement results accompanied by a sound uncertainty budget. In this study, such a procedure was developed for the quantification of total sulphur in copper using inductively coupled plasma-isotope dilution mass spectrometry (ICP-IDMS). For solving these problems ion exchange chromatography was applied, and a sulphur-matrix separation procedure was developed. This procedure was combined with ICP-IDMS to solve difficulties with the calibration and to realize metrological concepts. An application of the IDMS procedure was realized by using the measurement results of specific copper samples values for calibrating glow discharge mass spectrometry (GDMS) and laser ablation ICP-MS (LA-ICP-MS). Both techniques are considered routine techniques. Thus, they could provide reliable results which are traceable to the SI. Additionally, a procedure based on LA-ICP-IDMS was developed to significantly reduce the sample preparation step of ICP-IDMS with sulphur-matrix separation. This procedure is less laborious and the measurement results are still SI traceable and offer a comparatively high accuracy for LA-ICP-MS. Key for this development was the innovative application of polyethylene frits as support material for the dissolved sample. Thus, the quantification of sulphur in copper samples by LA-ICP-IDMS could be realized. The essential parameters are investigated such as the absorption efficiency of the frit and matrix effects. The developed procedure was fully validated by means of the ICP-IDMS results.

La tècnica de LA-ICP/MS presenta certs avantatges respecte altres tècniques d'anàlisi molt interessants per l'aplicació en el Camp de l'estudi del Patrimoni Cultural. Per una banda l'Ablació Laser aporta la possibilitat de la presa de mostra no manual, metodologia en moltes ocasions, més adequada en termes de destructivitat que els mètodes tradicionals. D'altra banda l'ús d'un ICP/MS com a detector aporta un nivell de sensibilitat per a la detecció de majoritaris i minoritaris però també de components en molt baixes concentracions que permet l'obtenció de resultats amb molt poca quantitat de mostra. Malgrat això, el seu ús per la caracterització materials d'objectes del Patrimoni Cultural està molt restringit i fins a dia d'avui només es troben estudis aplicats a objectes ceràmics, metàl·lics i algunes aproximacions a materials d'arxiu, però no en l'aplicació específica a obra pictòrica. Una de les restriccions més importants ve relacionada amb les dimensions dels objectes, en general massa grans per ser analitzats en equips comercials. Des d'un punt de vista analític existeixen dos aspectes importants a tenir present per la caracterització material d'aquest tipus d'objectes. Per una banda la heterogeneïtat intrínseca que presenten, fet que implica una complexitat important per la gran varietat de materials i estructures que es poden trobar. Per l'altre, la necessitat de conservar la integritat física, el que limita en molts casos la metodologia i procediments que es poden aplicar. En aquest context, l'objectiu d'aquesta tesi doctoral ha estat el desenvolupament d'un sistema de LA-ICP/MS per a la caracterització material no destructiva d'objectes del Patrimoni Cultural i la seva aplicació a diferents tipologies d'objectes, especialment a Pintura de Cavallet i Materials d'Arxiu. Dues de les aportacions més importants en el marc d'aquest treball han estat el desenvolupament d'un sistema òptic i la construcció d'una cel·la d'ablació. El sistema òptic permet dirigir el laser sobre un punt concret de l'objecte. A més permet també controlar tant el diàmetre del feix làser incident (diàmetre dels cràters d'ablació 100 µm) com la zona irradiada mitjançant una microcàmera de control. D'altra banda la cel·la d'ablació dissenyada és de fons obert i pot ser posicionada en qualsevol punt de l'objecte permetent l'anàlisi in situ sense restriccions en les seves mides, sense la necessitat d'extreure una mostra prèviament. Finalment l'aplicació de polsos successius sobre un mateix punt permet obtenir la informació estratigràfica, amb bona resolució espaial, tant en superfície com en profunditat. En l'aplicació a Pintura de Cavallet els objectius responen a l'avaluació del senyal obtingut, la capacitat d'identificar la composició tant de majoritaris com de minoritaris, així com la resolució en profunditat, per l'adquisició de la informació estratigràfica de capes pictòriques i de preparació, fent especial èmfasi en la capacitat de detectar capes primes com veladures. Aquesta fase es va dur a terme mitjançant l'anàlisi de pintures simulacre realitzades al laboratori i també amb obra real. En el cas d'obra real s'han analitzat dues pintures sobre taula, una amb tècnica al tremp Verge amb el nen i un àngel atribuïda a Jan Massys, i una a l'oli titulada Retrato de Piero de Medici 'il Gotoso', de Jacomo Pontormo. En ambdós casos s'ha determinat la composició tant de superfície com de capes subjacents i s'ha contribuït a la contextualització i atribució de les obres. En el cas de Material d'Arxiu, l'estudi s'ha centrat també en la caracterització material de manuscrits antics, fabricats a mà de draps i escrits amb tinta ferrogàl·lica. En aquest cas s'han estudiat les capacitats en termes de caracterització i distribució espaial en superfície, tant dels materials constitutius com dels efectes induïts per tractaments de conservació, en especial de desacidificació i laminació, avaluant els efectes de factors de corrosió i la seva influència en la conservació dels manuscrits. Per les dues aplicacions la tècnica ha aporta informació útil i es constitueix com una alternativa complementària a altres tècniques utilitzades en el camp com el SEM-EDX o FTIR.
Laser Ablation -ICP/MS is a technique which presents certain advantages regarding analysis of objects from Cultural Heritage field. In one hand the Laser Ablation device provides and alternative sampling procedure that may be more suitable for the analysis in this context. On the other hand the use of the ICP/MS as a detector, allows for the determination of the elemental composition in a wide range of concentrations with a minimum amount of material required. Nevertheless, its use for the material characterization of Cultural Heritage objects is highly restricted and only some experiences are published on the field of ceramic objects, metallic and some few cases study in manuscript analysis, but not on the analysis of paintings. One of the main drawbacks is the dimensions of the objects. As a consequence there are no commercially available instruments for LA-ICP/MS, including ablation cell, that permit the analysis of large objects like artworks neither Laser Ablation systems for “in situ” sampling had not been described until recently. From an analytical point of view, there are two primary concerns when characterizing works of art composition: the heterogeneity in the distribution of the components, at the macro and micro levels, and the need to preserve the physical integrity of each object In order to accomplish the analysis of objects regardless their size and material heterogenic composition, a specific optical system and ablation cell have been designed and coupled to the ICP/MS. The whole system has been applied on two different type of objects, easel Painting and Manuscripts, and some capabilities for each application evaluated. The capability of the developed LA-ICP/MS system for the analysis of paintings was evaluated in terms of damage produced on the artwork and its potential for stratigraphic composition determination by analyzing real painting such as the portrait of a member of the Medici Family attributed to Jacopo Pontormo, and a mannerist painting attributed to Jan Massys. Regarding the application to Manuscripts the main objective was the characterization of the original material composition and the effects of some restoration interventions in the pH, corrosion and degradation, evaluating the superficial resolution and the possibility to perform maps of the distribution. Results were compared with those obtained by SEM/EDX and FTIR.

The primary aim of this thesis is to develop image processing algorithms to quantitatively determine the link between traumatic brain injury (TBI) severity and chronic traumatic encephalopathy (CTE) neuropathology, specifically looking into the role of blood-brain barrier disruption following TBI. In order to causally investigate the relationship between the tau protein neurodegenerative disease CTE and TBI, mouse models of blast neurotrauma (BNT) and impact neurotrauma (INT) are investigated. First, a high-speed video tracking algorithm is developed based on K-means clustering, active contours and Kalman filtering to comparatively study the head kinematics in blast and impact experiments. Then, to compare BNT and INT neuropathology, methods for quantitative analysis of macroscopic optical images and fluorescent images are described. The secondary aim of this thesis focuses on developing methods for a novel application of metallomic imaging mass spectrometry (MIMS) to biological tissue. Unlike traditional modalities used to assess neuropathology, that suffer from limited sensitivity and analytical capacity, MIMS uses a mass spectrometer -- an analytical instrument for measuring elements and isotopes with high dynamic range, sensitivity and specificity -- as the imaging sensor to generate spatial maps with spectral (vector-valued) data per pixel. Given the vector nature of MIMS data, a unique end-to-end processing pipeline is designed to support data acquisition, visualization and interpretation. A novel multi-modal and multi-channel image registration (MMMCIR) method using multi-variate mutual information as a similarity metric is developed in order to establish correspondence between two images of arbitrary modality. The MMMCIR method is then used to automatically segment MIMS images of the mouse brain and systematically evaluate the levels of relevant elements and isotopes after experimental closed-head impact injury on the impact side (ipsilateral) and opposing side (contralateral) of the brain. This method quantifiably confirms observed differences in gadolinium levels for a cohort of images. Finally, MIMS images of human lacrimal sac biopsy samples are used for preliminary clinicopathological assessments, supporting the utility of the unique insights MIMS provides by correlating areas of inflammation to areas of elevated toxic metals. The image processing methods developed in this work demonstrate the significant capabilities of MIMS and its role in enhancing our understanding of the underlying pathological mechanisms of TBI and other medical conditions.
2019-07-09T00:00:00Z

Tooth enamel is among the most durable substances in the human body and as such has high recoverability in forensic anthropology cases. Its crystalline hydroxyapatite matrix has a slightly variable chemical composition which incorporates biologically available trace elements. The trace elements are derived from an individual's diet and the water he or she consumes during the period of enamel formation. As a result, trace element profiles of enamel can reflect the geology, pollution, and certain cultural dietary factors of the area in which the individual resided during this period. This research examines a sample of teeth with known demographic information from the Antioquia Modern Skeletal Reference Collection in Medellin, Colombia. A sample set of 75 teeth from 61 individuals born in areas throughout northwestern Colombia were analyzed using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), a minimally destructive, semi-quantitative technique. Analysis was performed at the Center for Archaeology, Materials, and Applied Spectroscopy (CAMAS) at Idaho State University. 33 elements were analyzed in the sample. Nonparametric methods were used to assess the relationship between elemental profiles and region of origin. Sr, Mo, Ag, Ba, Eu, and Tm concentration profiles were found to vary among regional groups. Al, Ni, Cr, Mn, Co, Sr, Cd, Sb, Sm, Eu, and U were found to predict region of origin. Differences in municipality were classified with 72% accuracy, variation across the department of Antioquia was classified with 67% accuracy, and the age of the geologic substrate was classified with 67% accuracy. The results suggest that trace element analysis of permanent tooth enamel may be of some use in estimating an individual's region of origin in forensic anthropological contexts. Further research with both larger sample sizes and more geographic variation is necessary.

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Many minor/trace elements can substitute into the crystal lattice of galena at various concentrations. In-situ LA-ICP-MS analysis and trace element mapping are used to obtain minor/trace element data from a range of natural galena specimens aiming to enhance understanding of the governing factors that control minor/trace element partitioning. The coupled substitution Ag+ + (Bi, Sb)3+ ↔ 2Pb2+, is confirmed by data obtained, although when Bi and/or Sb are present at high concentrations (~> 0.002 mol.%), site vacancies most likely come into play through the additional substitution 2(Bi, Sb)3+ + □ ↔ 3Pb2+. Galena is the primary host of Tl in all mapped mineral assemblages. Thallium is likely incorporated into galena along with Cu through the coupled substitution: (Ag, Cu, Tl)+ + (Bi, Sb)3+ ↔ 2Pb2+. Tin can reach significant concentrations in galena, particularly when the latter formed via metamorphic recrystallisation. Tin is concentrated in galena, likely via the substitution: Sn4+ + □ ↔ 2Pb2+, involving the creation of lattice vacancies, or Sn2+ ↔ Pb2+. Tin and In concentrations show a strong positive correlation across the sample suite indicating that the availability of these elements is intimately linked in natural systems. Cadmium and minor Hg can be incorporated into galena; the simple isovalent substitution (Cd, Hg)2+ ↔ Pb2+ is inferred. Significant oscillatory compositional zoning, and lesser sector zoning of minor/trace elements (Ag, Sb, Bi, Se, Te) is confirmed, for the first time, in galena from two epithermal ores. Zoning is attributed to slow crystal growth into open spaces within the vein at relatively low temperatures. The datasets generated increase understanding of the nature and distribution of minor/trace elements in galena, and partitioning between galena and coexisting minerals. These data have several applications in the minerals industry, particularly in studies of mineral deposit genesis, ore processing and, potentially, also in mineral exploration.
Thesis (B.Sc.(Hons)) -- University of Adelaide, School of Physical Scences, 2013

This investigation represents the first extensive application of Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry to ancient dental analysis and paleodietary reconstruction. Enamel strontium composition is examined because it is a reliable hard tissue indicator of diet during enamel formation in childhood. Here, infant diet and weaning behavior of pre-contact and colonial period Maya from Lamanai, Belize are reconstructed. Weaning is a critical dietary transition that has adaptive significance for later life. Since the strontium-calcium (Sr/Ca) ratio of solid food is high compared to that of breast milk, strontium composition of hard tissues developing before, and after, food supplementation can infer the timing of food introduction and weaning. Known timing of permanent enamel development allows correlation of canine enamel Sr/Ca values with age in childhood, which is facilitated by continuous laser microsampling. The results indicate that enamel Sr/Ca faithfully records a biogenic signal associated with childhood dietary intake. The total Sr/Ca pattern generally follows the projected model of strontium change, with food supplementation starting at around nine months of age, which increases gradually until there is a substantial surge in food intake at approximately two years of age. Lamanai children continue to nurse afterward, possibly up to five years of age, but it comprises a minor nutritional component. Significantly, the disadvantaged colonial Maya cohort has a reduced Sr/Ca pattern compared to elite Postclassic Maya, suggesting that colonial children may have exclusively breastfed for longer, delaying the age of food supplementation and weaning. Colonial Maya also exhibit greater Sr/Ca variation, reflecting dietary shifts that can be attributed to poorer nutrition and health. Female economic responsibilities partially account for the differences in colonial childcare practices. Additionally, enamel variation may reflect the different childhood origins (and weaning patterns) of possible migrants at Lamanai. Ultimately, the nature of infant diet and enamel Sr/Ca can be linked to interrelated ecological, political and economic factors. LA-ICP-MS analysis reveals enamel Sr/Ca to be a sensitive gauge of the prolonged and complex process of weaning and it proves to be an ideal method of capturing the richness of early life history documented in sequentially-formed enamel.

Ph.D. (Geology)
The successions of the Cape- and Karoo Supergroups preserve an integrated history of sedimentation along the paleo-Pacific margin of Gondwana from the Paleozoic to the Early Mesozoic. The Cape- and Karoo Supergroups have been well studied with regard to stratigraphy, sedimentary facies and depositional environment. However, the nature and location of their source regions, especially for the changeover from deposition within an Atlantic-type continental margin basin for the successions of the Cape Supergroup to an Andean-type continental foreland basin for some of the units of the Karoo Supergroup, remains poorly understood. In order to shed light on the nature of these source regions, a comprehensive U-Pb detrital zircon study of the successions of the Cape- and lower Karoo Supergroups was launched. A representative number of samples from the upper and lower successions of the Table Mountain- Bokkeveld- and Witteberg Groups of the Cape Supergroup as well as the Dwyka and Ecca Groups of the Karoo Supergroup were collected throughout the western, southwestern and southern Cape region. A few samples of the Dwyka Group were also collected within the more eastern outcrop regions of the succession located in Kwazulu-Natal. The sedimentary rocks of the Natal Group and Msikaba Formation have long been regarded as coeval with the Cape Supergroup. Similar to the successions of the Cape- and Karoo Supergroups, very little is known about their sedimentary source regions. Also, their relative age of sedimentation remains poorly constrained. The U-Pb detrital zircon study of the successions of the Cape- and lower Karoo Supergroups was thus extended so as to include the successions of the Natal Group and Msikaba Formation. The detrital zircon age populations of the successions of the Natal Group and Msikaba Formation would not only improve the present understanding with regards to the sedimentary source regions to these units but would also facilitate the evaluation of possible correlations between these units and the stratigraphic units of the Cape Supergroup. Samples of both the lower Durban Formation and the upper Mariannhill Formation of the Natal Group and the Msikaba Formation (which is presently regarded as being part of the Cape Supergroup) were therefore collected within their respective outcrop regions in the Kwazulu-Natal area. The similarities in litho- and bio-stratigraphy between the successions of the Cape- and Karoo Supergroups and those of the Ordovician to Early Permian successions of the Ventania System and the Ordovician to Silurian successions of the Tandilia System in Argentina have long been recognized. Although the detrital zircon populations of some of the formations within these Systems have been evaluated in the past, it is yet to be determined whether these successions and those of the Cape- and lower Karoo Supergroups have certain source regions in common. In order to facilitate such a comparison, samples of selected units of the Ventania System were therefore collected near Sierra de la Ventania, while a sample of the Balcarce Formation of the Tandilia System was obtained near Mar del Plata. The detrital zircon age populations of the successions of the Ventania and Tandilia Systems were also further evaluated in the light of establishing or confirming a time-correlation between these formations and those of the Cape- and lower Karoo Supergroups. U-Pb age determination of the detrital zircons population of the samples was conducted by means of Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS). Although LA-ICP-MS is a routine, well-established technique where the U-Pb age determination of detrital zircons is concerned, it was yet to be established at the centralized analytical facility of the University of Johannesburg, SPECTRUM, using the instrumentation currently available (i.e. 213nm Nd:YAG laser coupled to Quadrupole-based ICP-MS). The U-Pb age determination of detrital zircons was therefore preceded by a fair amount of instrument optimization and method development. Well studied shortcomings of U-Pb detrital zircon dating by LA-ICP-MS such as laser induced elemental fractionation, mass discrimination effects and as well as the possible occurrence of minor common-Pb needs were addressed and corrected for. The detrital zircon populations of successions in the Cape Supergroup have a distinct major Neoproterozoic to Early Cambrian age component, which can be attributed to an input of detritus from successions related to the Pan-African Orogeny in South Africa, such as the Gariep- and Saldania Belts located towards the north of the Cape Basin. A substantial amount of Mesoproterozoic detrital zircon grains is also present in all the samples from the successions of the Cape Supergroup. These grains of Mesoproterozoic age were probably derived from the Namaqua-Natal Metamorphic Province, which is also regarded as the source of some minor amounts of Paleoproterozoic detrital zircon grains. The near absence of Archean grains from the detrital zircon populations of the successions of the Cape Supergroup is notable, and is thought to be due to the Namaqua-Natal Metamorphic Province acting as a geomorphological barrier at the time of their deposition. The minor Paleozoic (Ordovician to Carboniferous) detrital zircon populations in the samples from the formations of the Cape Supergroup increase progressively upwards through the succession. ....

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The Telfer Au-Cu deposit, Paterson Province, W.A. is hosted within two doubly-plunging anticlines, the Main Dome and the West Dome. The deposit consists of vertically-stacked, stratabound Au-Cu mineralised horizons ('reefs') linked by associated stockwork, sheeted and discordant veins. The study targeted a better petrographic, mineralogical and geochemical understanding of pyrite and chalcopyrite in E-Reefs mineralization with the objective of placing additional constraints on ore genesis. Particular emphasis is placed on Type-4 pyrite as defined by Fargher (2012), notably the speciation of mineral inclusions within this type and their significance for a genetic model involving granitoid-sourced fluids. The trace element chemistry of the associated chalcopyrite was characterised by Laser-Ablation Inductively-Coupled Plasma Mass-Spectrometry (LA-ICP-MS) to identify whether a similar signature is present. Back-scatter electron imaging established a number of mineral associations and inclusions within pyrite and chalcopyrite. These define a pronounced Sn-Bi-Ag geochemical signature in the E-Reefs. LA-ICP-MS data for pyrite, and particularly chalcopyrite, from the E-Reefs exhibit the same Sn-Ag-Bi geochemical signature and are indicative of a granitophile character. Such a signature is unlike that of the Middle Vale Reef. Arsenopyrite- and gersdorffite-bearing assemblages within crosscutting veins indicate a superposed hydrothermal event, in which additional elements, like As, were introduced to the system. There is also evidence of extensive ore remobilisation as the result of a later thermal event. These findings support a modified model of ore genesis for the Telfer deposit in which not all components in the ore fluid were leached from the surrounding sedimentary rocks but also involve fluids from adjacent granites. This has application not only to the Telfer deposit but carries implications for other ore systems in the Paterson Province. Results also contribute to ongoing work 'fingerprinting' chalcopyrite from different ore types to establish a basis for discriminating metal sources and fluid evolution.
Thesis (B.Sc.(Hons)) -- University of Adelaide, School of Physical Sciences, 2014