Mapping environmental suitability for anthrax reemergence in the Arctic

Recent studies have raised concerns about the potential reemergence of infectious diseases in Arctic regions associated with warming temperatures. Among these, particular attention has been devoted to anthrax, as a consequence of the outbreak that occurred in the Russian Yamalo-Nenets peninsula in 2016. Understanding how environmental change might influence the diffusion of this pathogen could allow informed decisions to prevent further zoonotic or epidemic episodes. To that end, the present study aims to identify and investigate the driving variables that may favor anthrax transmission within the Arctic, in order to build environmental niche maps describing the future suitability of these regions for the pathogen. To do so, we use the MaxEnt statistical learning tool informed by Arctic-specific variables, such as reindeer herd distribution and active-layer variation. Because of the relative lack of reliable georeferenced information in these regions, the resulting potential distribution maps are to be considered preliminary, but they can already provide a first assessment tool for local communities living in potential risk areas. They also indicate areas in which additional investigation is needed to improve the reliability of environmental niche modeling, hence the accuracy of risk mapping and the usefulness to Arctic communities

Determination of Fe2+ and Fe3+ species by FIA-CRC-ICP-MS in Antarctic ice samples

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Characterization of organic-rich mineral debris revealed by rapid glacier retreat, Indren Glacier, European Alps

In the summer of 2003 and 2004, characterized by a rapid glacier retreat, a stony surface covered by well-structured organic-rich mineral debris was observed very close to the Indren glacier terminus (Monte Rosa Massif, NW Italy, 3100 m ASL), on an area covered by the glacier tongue till the year before. The origin and type of this organic-rich material were investigated, in order to detect their characteristics, potential sources and fate within the foreland system. The deposits were dated using Carbon-14 and analyzed for the chemical characteristics of the organic component, the elemental composition of the mineral fraction and presence of microbial markers. The material, granular and dark in color, had a total organic carbon (TOC) content ranging between 17.4 ± 0.39 and 28.1 ± 0.63 g kg$^{−1}$ dry weight (dw), significantly higher than the surrounding glacial till (~ 1.4 g kg$^{−1}$ dw), although only 0.33% of it was in water soluble form. Microbial carbon (C) and nitrogen (N) accounted for 10.6% and 3.13% of TOC and total N, respectively. Dissolved nitrogen (N), mainly present as ammonium, represented 2.40% of the total N. The low aromatic component and large presence of nitrogen (N)-derived compounds suggested that most of the organic carbon (OC) in these organic-rich mineral deposits was derived from microbial cells, although the high average radiocarbon age of about 2900 years may also point to the contribution of aeolian depositions of anthropogenic or natural origin. Elemental composition and the crustal enrichment factor of trace elements in the mineral fraction of the aggregates corroborated the hypothesis that most part of the accumulated material derived from ice meltwater. Some indicators of the colonization of these deposits by microbial communities were also reported, from the abundance of DNA and phylogenetic markers, to the presence of bacterial taxa commonly able to thrive in similar habitats. All these elements suggested that such kind of deposits may have a potential role as energy and nutrient sources in recently deglaciated areas, highlighting the necessity to better understand the processes underlying their formation and their evolution

Fast Liquid Chromatography Coupled with Tandem Mass Spectrometry for the Analysis of Vanillic and Syringic Acids in Ice Cores

The development of new analytical systems and the improvement of the existing ones to obtain high-resolution measurements of chemical markers in samples from ice cores, is one of the main challenges the paleoclimatic scientific community is facing. Different chemical species can be used as markers for tracking emission sources or specific environmental processes. Although some markers, such as methane sulfonic acid (a proxy of marine productivity), are commonly used, there is a lack of data on other organic tracers in ice cores, making their continuous analysis analytically challenging. Here, we present an innovative combination of fast liquid chromatography coupled with tandem mass spectrometry (FLC-MS/MS) to continuously determine organic markers in ice cores. After specific optimization, this approach was applied to the quantification of vanillic and syringic acids, two specific markers for biomass burning. Using the validated method, detection limits of 3.6 and 4.6 pg mL–1 for vanillic and syringic acids, respectively, were achieved. Thanks to the coupling of FLC-MS/MS with the continuous flow analytical system, we obtained one measurement every 30 s, which corresponds to a sampling resolution of a sample every 1.5 cm with a melting rate of 3.0 cm min–1. To check the robustness of the method, we analyzed two parallel sticks of an alpine ice core over more than 5 h. Vanillic acid was found with concentrations in the range of picograms per milliliter, suggesting the combustion of coniferous trees, which are found throughout the Italian Alps.publishedVersio

Chemical and Lead Isotope characterisation of First World War shrapnel balls and bullets used on the Alpine Austrian\u2013Italian Front

Chemical and lead isotope characterisation was carried out on shrapnel balls and bullets dating back to the First World War (WWI). These ammunitions were widely utilised in the Alpine Austrian\u2013Italian front located in the Italian Alps. The investigation has been performed using inductively coupled plasma quadrupole mass spectrometry equipped with an octopole reaction system (ORS-ICP-QMS). The main goal of this work was to identify the elemental and lead isotope composition of raw materials and to discriminate between the military objects analysed. The results of multi-elemental analysis indicate that the shrapnel ball samples consisted of soft Pb or hard Pb with Sb depending on the use, the weapon type and the specific nation. The Italian shrapnel balls were made from hard Pb, as opposed to those of the Austrian\u2013 Hungarian samples. Through the investigation of lead isotope ratios, it has been possible to differentiate most of the Italian shrapnel balls from those of Austrian\u2013 Hungarian origin. Furthermore, some Italian shrapnel balls had a different lead isotope composition depending on their calibre. The elemental composition and lead isotopic signature of bullets show a clear discrimination between the external jacket and the core in relation to projectile type and nationality. The bullet cores consist of 164 Scientia Militaria, South African Journal of Military Studies, Vol 46, Nr 1, 2018. doi: 10.5787/46-1-1230 Pb\u2013Sb alloy regardless of the region of origin. This work allowed us to investigate the potential applications of trace elements and lead isotope analyses to discriminate military artefacts of different origin

Chemical and lead isotope characterisation of First World War shrapnel balls and bullets used on the Alpine Austrian–Italian Front

Chemical and lead isotope characterisation was carried out on shrapnel balls and bullets dating back to the First World War (WWI). These ammunitions were widely utilised in the Alpine Austrian–Italian front located in the Italian Alps. The investigation has been performed using inductively coupled plasma quadrupole mass spectrometry equipped with an octopole reaction system (ORS-ICP-QMS). The main goal of this work was to identify the elemental and lead isotope composition of raw materials and to discriminate between the military objects analysed. The results of multi-elemental analysis indicate that the shrapnel ball samples consisted of soft Pb or hard Pb with Sb depending on the use, the weapon type and the specific nation. The Italian shrapnel balls were made from hard Pb, as opposed to those of the Austrian– Hungarian samples. Through the investigation of lead isotope ratios, it has been possible to differentiate most of the Italian shrapnel balls from those of Austrian– Hungarian origin. Furthermore, some Italian shrapnel balls had a different lead isotope composition depending on their calibre. The elemental composition and lead isotopic signature of bullets show a clear discrimination between the external jacket and the core in relation to projectile type and nationality. The bullet cores consist of  Pb–Sb alloy regardless of the region of origin. This work allowed us to investigate the potential applications of trace elements and lead isotope analyses to discriminate military artefacts of different origins.Keywords: ICP-MS, trace element, source identification, principal component analysis, forensic scienc

An upgraded CFA - FLC - MS/MS system for the semi-continuous detection of levoglucosan in ice cores

A new Continuous Flow Analysis (CFA) system coupled with Fast Liquid Chromatography – tandem Mass Spectrometry (FLC-MS/MS) has been recently developed for determining organic markers in ice cores. In this work we present an upgrade of this innovative technique, optimized for the detection of levoglucosan in ice cores, a crucial tracer for reconstructing past fires. The upgrade involved a specific optimization of the chromatographic and mass spectrometric parameters, allowing for a higher sampling resolution (down to 1 cm) and the simultaneous collection of discrete samples, for off-line analysis of water stable isotopes and additional chemical markers. The robustness and repeatability of the method has been tested by the analysis of multiple sticks of ice cut from the same shallow alpine ice core, and running the system for several hours on different days. The results show similar and comparable trends between the ice sticks. With this upgraded system, a higher sensitivity and a lower limit of detection (LOD) was achieved compared to discrete analysis of alpine samples for levoglucosan measurements. The new LOD was as low as 66 ng L−1, a net improvement over the previous LOD of 600 ng L−1