scholarly journals Depot medených predmetov z Mníchovej Lehoty (okr. Trenčín). Príspevok k poznaniu antimónovej medi typu Nógrádmarcal v období staršieho eneolitu / Depotfund von Kupfergegenständen aus Mníchova Lehota (Bez. Trenčín). Beitrag zur Erkennung des Antimonkupfers vom Typ Nógrádmarcal in dem älteren Aeneolithikum

2021 ◽  
Vol 112 ◽  
pp. 301-332
Author(s):  
Mária Novotná ◽  
Tomáš Zachar ◽  
Ján Dzúrik ◽  
Martin Kvietok

Hoard of Copper Artefacts from Mníchova Lehota (Distr. Trenčín). Contribution to the Issue and Distribution of the Antimony Copper of Nógrádmarcal Type in the Early Copper Age. Submitted paper deals with the archaeological evaluation and elemental analysis of a collection of copper industry from the cadastre of municipality Mníchova Lehota (distr. Trenčín) in the north-west Slovakia. The hoard consists of two flat copper axes and a copper chisel. The basic typological-chronological analysis of the flat copper axes showed their connection with the Southeast European types and varieties of the series Pločnik, Coteana, Gumelniţa, as well as Central European types Stollhof, Strážnice, Kalinowice Dolne and axes of the group III of J. Říhovský. Statistical evaluation of basic morphometric parameters of the artefacts by means of principal component analysis (PCA) suggests that the objects from the hoard from Mníchova Lehota belong to the Central European shapes. Separate issue is the elemental analysis of the copper artefacts by means of inductively coupled plasma – mass spectrometry (ICP-MS) and X-ray fluorescence spectroscopy (XRF). On the basis of the statistical evaluation of the elemental analyses the authors set the origin of the copper material mainly in the antimonic copper. They pay attention to its distribution in the area of Central Europe and possible location of the copper material deposit.

2020 ◽  
Author(s):  
Joshua D'Uva ◽  
David DeTata ◽  
Christopher D. May ◽  
Simon W. Lewis

<p>In Australia, party sparklers are commonly used to initiate or prepare inorganic based homemade explosives (HMEs) as they are the most easily accessible and inexpensive pyrotechnic available on the market. As sparkler residue would be encountered in cases involving these types of devices, the characterisation and source determination of the residue would be beneficial within a forensic investigation. The aim of this study is to demonstrate the potential of using trace elemental profiling coupled with chemometric and other statistical techniques to link a variety of different sparklers to their origin. Inductively coupled plasma – mass spectrometry (ICP-MS) was used to determine the concentration of 50 elements in 48 pre-blast sparkler samples from eight sparkler brands/classes available in Australia. Extracting ground-up sparkler residue in 10% nitric acid for 24 hours was found to give the most reliable quantification. The collected data were analysed using Principal Component Analysis (PCA) to visualise the distribution of the sample data and explore whether the sparkler samples could be classified into their respective brands. ANOVA based feature selection was used to remove elements that did not significantly contribute to the separation between classes. This resulted in the development of a 7-elemental profile, consisting of V, Co, Ni, Sr, Sn, Sb, W, which could be used to correctly classify the samples into eight distinct groups. Linear Discriminant Analysis (LDA) was subsequently used to construct a discriminant model using four out of six samples from each class. The model successfully classified 100% of the samples to their correct sparkler brand. The model also correctly matched 100% of the remaining samples to the correct class. This demonstrates the potential of using trace elemental analysis and chemometrics to correctly identify and discriminate between party sparklers. </p>


2020 ◽  
Author(s):  
Joshua D'Uva ◽  
David DeTata ◽  
Christopher D. May ◽  
Simon W. Lewis

<p>In Australia, party sparklers are commonly used to initiate or prepare inorganic based homemade explosives (HMEs) as they are the most easily accessible and inexpensive pyrotechnic available on the market. As sparkler residue would be encountered in cases involving these types of devices, the characterisation and source determination of the residue would be beneficial within a forensic investigation. The aim of this study is to demonstrate the potential of using trace elemental profiling coupled with chemometric and other statistical techniques to link a variety of different sparklers to their origin. Inductively coupled plasma – mass spectrometry (ICP-MS) was used to determine the concentration of 50 elements in 48 pre-blast sparkler samples from eight sparkler brands/classes available in Australia. Extracting ground-up sparkler residue in 10% nitric acid for 24 hours was found to give the most reliable quantification. The collected data were analysed using Principal Component Analysis (PCA) to visualise the distribution of the sample data and explore whether the sparkler samples could be classified into their respective brands. ANOVA based feature selection was used to remove elements that did not significantly contribute to the separation between classes. This resulted in the development of a 7-elemental profile, consisting of V, Co, Ni, Sr, Sn, Sb, W, which could be used to correctly classify the samples into eight distinct groups. Linear Discriminant Analysis (LDA) was subsequently used to construct a discriminant model using four out of six samples from each class. The model successfully classified 100% of the samples to their correct sparkler brand. The model also correctly matched 100% of the remaining samples to the correct class. This demonstrates the potential of using trace elemental analysis and chemometrics to correctly identify and discriminate between party sparklers. </p>


2020 ◽  
Author(s):  
Joshua D'Uva ◽  
David DeTata ◽  
Christopher D. May ◽  
Simon W. Lewis

<p>In Australia, party sparklers are commonly used to initiate or prepare inorganic based homemade explosives (HMEs) as they are the most easily accessible and inexpensive pyrotechnic available on the market. As sparkler residue would be encountered in cases involving these types of devices, the characterisation and source determination of the residue would be beneficial within a forensic investigation. The aim of this study is to demonstrate the potential of using trace elemental profiling coupled with chemometric and other statistical techniques to link a variety of different sparklers to their origin. Inductively coupled plasma – mass spectrometry (ICP-MS) was used to determine the concentration of 50 elements in 48 pre-blast sparkler samples from eight sparkler brands/classes available in Australia. Extracting ground-up sparkler residue in 10% nitric acid for 24 hours was found to give the most reliable quantification. The collected data were analysed using Principal Component Analysis (PCA) to visualise the distribution of the sample data and explore whether the sparkler samples could be classified into their respective brands. ANOVA based feature selection was used to remove elements that did not significantly contribute to the separation between classes. This resulted in the development of a 7-elemental profile, consisting of V, Co, Ni, Sr, Sn, Sb, W, which could be used to correctly classify the samples into eight distinct groups. Linear Discriminant Analysis (LDA) was subsequently used to construct a discriminant model using four out of six samples from each class. The model successfully classified 100% of the samples to their correct sparkler brand. The model also correctly matched 100% of the remaining samples to the correct class. This demonstrates the potential of using trace elemental analysis and chemometrics to correctly identify and discriminate between party sparklers. </p>


The Holocene ◽  
2011 ◽  
Vol 21 (7) ◽  
pp. 1037-1048 ◽  
Author(s):  
Bergrún Arna Óladóttir ◽  
Olgeir Sigmarsson ◽  
Gudrún Larsen ◽  
Jean-Luc Devidal

The Holocene eruption history of subglacial volcanoes in Iceland is largely recorded by their tephra deposits. The numerous basaltic tephra offer the possibility to make the tephrochronology in the North Atlantic area more detailed and, therefore, more useful as a tool not only in volcanology but also in environmental and archaeological studies. The source of a tephra is established by mapping its distribution or inferred via compositional fingerprinting, mainly based on major-element analyses. In order to improve the provenance determinations for basaltic tephra produced at Grímsvötn, Bárdarbunga and Kverkfjöll volcanic systems in Iceland, 921 samples from soil profiles around the Vatnajökull ice-cap were analysed for major-element concentrations by electron probe microanalysis. These samples are shown to represent 747 primary tephra units. The tephra erupted within each of these volcanic system has similar chemical characteristics. The major-element results fall into three distinctive compositional groups, all of which show regular decrease of MgO with increasing K2O concentrations. The new analyses presented here considerably improve the compositional distinction between products of the three volcanic systems. Nevertheless, slight overlap of the compositional groups for each system still remains. In situ trace-element analyses by laser-ablation-inductively-coupled-plasma-mass-spectrometry were applied for better provenance identification for those tephra having similar major-element composition. Three trace-element ratios, Rb/Y, La/Yb and Sr/Th, proved particularly useful. Significantly higher La/Yb distinguishes the Grímsvötn basalts from those of Bárdarbunga and Rb/Y values differentiate the basalts of Grímsvötn and Kverkfjöll. Additionally, the products of Bárdarbunga, Grímsvötn and Kverkfjöll form distinct compositional fields on a Sr/Th versus Th plot. Taken together, the combined use of major- and trace-element analyses in delineating the provenance of basaltic tephra having similar major-element composition significantly improves the Holocene tephra record as well as the potential for correlations with tephra from outside Iceland.


Author(s):  
Sarah C. Swan ◽  
John D.M. Gordon ◽  
Beatriz Morales-Nin ◽  
Tracy Shimmield ◽  
Terrie Sawyer ◽  
...  

Otoliths were obtained from Nezumia aequalis, a small macrourid that is widely distributed throughout the Atlantic and Mediterranean—two very different physical environments. Microchemical analysis of the otoliths was carried out using solution-based inductively coupled plasma mass spectrometry of whole otoliths. Significant differences between fish populations were found for concentrations of the elements Li and Sr. Only 54% of the samples were correctly classified by area using discriminant analysis. Otolith samples from the Reykjanes Ridge were most easily distinguished. The results are discussed in relation to trace element concentrations in the waters of the north-eastern Atlantic Ocean and the Mediterranean Sea.


2021 ◽  
pp. 1-27
Author(s):  
Aranya Sen ◽  
Koushik Sen ◽  
Amitava Chatterjee ◽  
Shubham Choudhary ◽  
Alosree Dey

Abstract The Himalaya is characterized by the presence of both pre-Himalayan Palaeozoic and syn-Himalayan Cenozoic granitic bodies, which can help unravel the pre- to syn-collisional geodynamics of this orogen. In the Bhagirathi Valley of Western Himalaya, such granites and the Tethyan Himalayan Sequence (THS) hosting them are bound to the south by the top-to-the-N extensional Jhala Normal Fault (JNF) and low-grade metapelite of the THS to its north. The THS is intruded by a set of leucocratic dykes concordant to the JNF. Zircon U–Pb laser ablation multi-collector inductively coupled plasma mass spectrometry (LA-MC-ICP-MS) geochronology of the THS and one leucocratic dyke reveals that the two rocks have a strikingly similar age distribution, with a common and most prominent age peak at ~1000 Ma. To the north of the THS lies Bhaironghati Granite, a Palaeozoic two-mica granite, which shows a crystallization age of 512.28 ± 1.58 Ma. Our geochemical analysis indicates that it is a product of pre-Himalayan Palaeozoic magmatism owing to extensional tectonics in a back-arc or rift setting following the assembly of Gondwana (500–530 Ma). The Cenozoic Gangotri Leucogranite lies to the north of Bhaironghati Granite, and U–Pb dating of zircon from this leucogranite gives a crystallization age of 21.73 ± 0.11 Ma. Our geochemical studies suggest that the Gangotri Leucogranite is a product of muscovite-dehydration melting of the lower crust owing to flexural bending in relation to steepening of the subducted Indian plate. The leucocratic dykes are highly refracted parts of the Gangotri Leucogranite that migrated and emplaced along extensional fault zones related to the JNF and scavenged zircon from the host THS during crystallization.


Sign in / Sign up

Export Citation Format

Share Document