Ablation Inductively Coupled Plasma Mass Spectrometry Research Articles

Endodermal suberin restricts root leakage of cesium: a suitable tracer for potassium.

An urgent challenge within crop production is to maintain productivity in a world plagued by climate change and its associated plant stresses, such as heat, drought and salinity. A key factor in this endeavor is to understand the dynamics of root suberization, and its role in plant-water relations and nutrient transport. This study focuses on the hypothesis that endodermal suberin, acts as a physical barrier preventing radial potassium (K) movement out of the vascular tissues during translocation. Previous attempts to experimentally support this idea have produced inconsistent results. We developed a Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS) method, allowing us to visualize the distribution of mineral elements and track K movement. Cesium (Cs), dosed in optimized concentrations, was found to be an ideal tracer for K, due to its low background and similar chemical/biological properties. In suberin mutants of Arabidopsis thaliana, we observed a positive correlation between suberin levels and K translocation efficiency, indicating that suberin enhances the plant's ability to retain K within the vascular tissues during translocation from root to shoot. In barley (Hordeum vulgare), fully suberized seminal roots maintained higher K concentrations in the stele compared to younger, less suberized root zones. This suggests that suberization increases with root maturity, enhancing the barrier against K leakage. In nodal roots, suberin was scattered towards the phloem in mature root zones. Despite this incomplete suberization, nodal roots still restrict outward K movement, demonstrating that even partial suberin barriers can significantly reduce K loss. Our findings provide evidence that suberin is a barrier to K leakage during root-to-shoot translocation. This understanding is crucial to maintain crop productivity in the face of climate change.

Juvenile downstream migration patterns of an anadromous fish, allis shad (Alosa alosa), before and after the population collapse in the Gironde system, France.

Diadromous fish have exhibited a dramatic decline since the end of the 20th century. The allis shad (Alosa alosa) population in the Gironde-Garonne-Dordogne (GGD) system, once considered as a reference in Europe, remains low despite a fishing ban in 2008. One hypothesis to explain this decline is that the downstream migration and growth dynamics of young stages have changed due to environmental modifications in the rivers and estuary. We retrospectively analysed juvenile growth and migration patterns using otoliths from adults caught in the GGD system 30 years apart during their spawning migration, in 1987 and 2016. We coupled otolith daily growth increments and laser ablation inductively-coupled plasma mass spectrometry measurements of Sr:Ca, Ba:Ca, and Mn:Ca ratios along the longest growth axis from hatching to an age of 100 days (i.e., during the juvenile stage). A back-calculation allowed us to estimate the size of juveniles at the entrance into the brackish estuary. Based on the geochemistry data, we distinguished four different zones that juveniles encountered during their downstream migration: freshwater, fluvial estuary, brackish estuary, and lower estuary. We identified three migration patterns during the first 100 days of their life: (a) Individuals that reached the lower estuary zone, (b) individuals that reached the brackish estuary zone, and (c) individuals that reached the fluvial estuary zone. On average, juveniles from the 1987 subsample stayed slightly longer in freshwaterthan juveniles from the 2016 subsample. In addition, juveniles from the 2016 subsample entered the brackish estuary at a smaller size. This result suggests that juveniles from the 2016 subsample might have encountered more difficult conditions during their downstream migration, which we attribute to a longer exposure to the turbid maximum zone. This assumption is supported by the microchemical analyses of the otoliths, which suggests based on wider Mn:Ca peaks that juveniles in 2010s experienced a longer period of physiological stress during their downstream migration than juveniles in 1980s. Finally, juveniles from the 2016 subsample took longer than 100 days to exit the lower estuary than we would have expected from previous studies. Adding a new marker (i.e., Ba:Ca) helped us refine the interpretation of the downstream migration for each individual.

Mineralogy and elemental geochemistry of pyrite coal-balls, Datong Coalfield, Shanxi Province, China: Implications for differentiation mechanism

The pyrite coal-balls found in No.9 coal of Taiyuan Formation in Dongzhouyao Mine of Datong Coalfield were selected to investigate its mineralogy and elemental geochemistry using optical microscope observation, scanning electron microscopy combined with an energy-dispersive X-ray spectrometer (SEM-EDX), inductively coupled plasma mass spectrometry analysis (ICP-MS), laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS), and electron probe micro-analysis (EPMA). Due to the high content of pyrite, the major-element oxides in the coal-ball samples were mainly Fe2O3, with an average of 62.68 %. LA-ICP-MS results showed that coal-balls were enriched in Tl (CC = 32.79), Pb (CC = 9.22), and Mo (CC = 2.07), while the coals in the same layer were enriched in Ga (CC = 5.31), Tl (CC = 3.66), and Li (CC = 2.27). Affinities to S or Fe and the variation of elemental concentration in the environment during the formation of coal-balls were the primary factor of the elemental differentiation between coals and coal-balls, as well as within coal-balls. The coal-balls formed in four stages in a marine-continental transition environment, with Fe from terrestrial sources and S from marine phases, and its physical origin is basically consistent with that of some Carboniferous-Permian coals in the Datong Coalfield. According to the formation sequence and geochemical characteristics, four periods of pyrite coal-balls evolution have been proposed.

Improving the chronostratigraphic framework of the Transvaal Supergroup (South Africa) through in-situ and high-precision U-Pb geochronology

The Transvaal Supergroup, on the Kaapvaal Craton in South Africa, is widely accepted as one of the best-preserved sedimentary archives to constrain planetary-scale environmental changes during the late Archean and early Proterozoic, yet the sedimentation age for certain stratigraphic intervals remains poorly constrained. To improve the temporal control on some of the first-order global changes recorded in these rocks, we carried out U-Pb analyses of detrital zircon populations from several clastic and volcano-clastic sedimentary units of the Transvaal Supergroup. We applied the Chemical Abrasion-Isotope Dilution-Thermal Ionization Mass Spectrometry (CA-ID-TIMS) technique on detrital and volcanic zircon populations that had been previously screened using the Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS) technique. We report new maximum depositional age estimates for the Pannetjie (2456.6 ± 7.0 Ma), the Heynskop (2451.5 ± 2.5 Ma), the Makganyene (2423.1 ± 1.0 Ma) and the Hekpoort formations (2248.0 ± 1.1 Ma).A ca. 2.25 Ga-old cluster of LA-ICP-MS analyses in the Makganyene Formation was identified to be spurious, since it was completely removed during the chemical abrasion. Thus, we speculate that circulation of hydrothermal fluids and associated Pb-loss from a radiation-damaged lattice during the emplacement of the much younger Hekpoort Formation or possibly the Ophthalmia Orogeny, recorded in Western Australia, may have reset the U-Pb system of this zircon population. This implies that the accurate maximum depositional age of the Makganyene Formation is ca. 2.42 Ga instead, which denotes the age of the oldest glacial event of global extent during the Paleoproterozoic. Therefore, we suggest that the combination of both dating techniques is essential to ensure accurate maximum depositional age constraints for ancient detrital sedimentary rocks. Additionally, our data provides temporal constraints on a period characterized by major fluctuations in atmospheric oxygen. Finally, and supporting the complex nature of the Paleoproterozoic, linkages between widespread glaciations and atmospheric oxygen fluctuations remain to be explored.

Obsidian exchange networks and highland-lowland interaction in the Lesser Caucasus borderlands

Obsidian sourcing studies have a long history in the Near East, but relatively few have focused on obsidian exchange after the Early Bronze Age. Here, we present a multi-technique analysis of an assemblage of 111 obsidian artifacts from excavated Late Bronze and Early Iron Age (LBA-EIA; c. 15th-6th c BCE) contexts at Mtsvane Gora, southern Georgia. Because the site is situated in the lowland Kura Valley and the nearest obsidian sources are in the highlands to the south and west, obsidian provenance can serve as a proxy for mapping highland-lowland interactions. Chemical compositions analyzed via portable X-ray fluorescence spectrometry (pXRF), electron microprobe analysis (EMPA), and laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS), were compared with existing geological datasets of chemical analyses to identify the source of all but one of the artifacts analyzed. The results show that Chikiani, a source in the highlands of southern Georgia, was the geological origin of >90% of the objects analyzed. While acknowledging that obsidian exchange is just one aspect of highland-lowland interaction, this finding implies that Mtsvane Gora’s connections with the adjacent highlands were skewed towards greater engagement with some highland areas relative to others. More generally, the research suggests that geographic adjacency of highlands and lowlands does not necessarily mean that they were highly interconnected.

Examining the Nasca religious network on the south coast of Peru: LA-ICP-MS of Early Nasca ceramics from the Upper Ica Valley (AD 250–450)

This study investigates the geographic extent of a hypothesized pilgrimage network on the south coast of Peru during the Early Intermediate Period (AD 100-650), centered around the important ceremonial site of Cahuachi. It has been argued that Early Nasca style ceramics were manufactured here and distributed to pilgrims from surrounding Southern Nasca Region (SNR) villages as symbols of their pilgrimage, and daily reminders of the Cahuachi ideology. However, the participation of people from other, more distant parts of the Nasca homeland, including the Upper Ica Valley, has not been tested. We do so here by conducting a compositional study using Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS) on ceramics from two Upper Ica Valley sites, Cerro Soldado and Cerro Tortolita. The results indicate that ceramics recovered from the SNR and the Upper Ica Valley are chemically distinct, supporting different raw material sources and production zones. Furthermore, our results indicate that pottery produced with SNR raw materials is not present at either site. These findings lead us to reassess the direct reach of Cahuachi’s pilgrimage network, and the importance of production centers outside of Cahuachi for contributing to the Nasca iconography and culture.

Distribution of Li, Ga, Nb, and REEs in coal as determined by LA-ICP-MS imaging: A case study from Jungar coalfield, Ordos Basin, China

Previous studies on modes of occurrence of Li, Ga, and Nb in coal are primarily based upon statistical analyses due to the low concentrations of these elements and the lack of methods of direct analysis. Laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) can be used for the in-situ determination of trace elements in minerals. The strong heterogeneity and diversity of macerals lead to a lack of suitable internal calibration elements required for LA-ICP-MS-based analysis of trace elements in coal, making the determination of trace elements in organic matter in coal challenging. In this study, the previously investigated high-Al and Li-Ga-Nb enriched No. 6 coal in the Haerwusu Mine of the Jungar Coalfield, Ordos Basin, China, was chosen for revealing the distribution and modes of occurrence of Li, Ga, Nb, and rare earth elements (REEs; REY if Y included) in coal, using the LA-ICP-MS method of mapping (imaging) technology. The results indicate that the majority of Ga and Nb present within the coal was concentrated within a specific collotelinite layer. Gallium and Nb have an organic association and are rare within minerals (i.e., clay minerals and boehmite). Lithium is homogeneously distributed throughout the clay minerals in the collodetrinite. Most of the La and Ce in the coal are concentrated in La- and Ce-enriched minerals, including monazite, bastnaesite, and lanthanite. The other REEs are concentrated in the Ga- and Nb-enriched collotelinite, along with small amounts of La and Ce. A similar characterization processing may be used to determine the modes of occurrences of trace elements in other organic-rich rocks or fine-grained sediments.

Progresses in Fluid Inclusion Synthesis in Quartz

High-temperature and high-pressure (HTHP) fluids are one of the most extensive participants in geological events. The representative in situ sampling of the HTHP fluids, which is an essential prerequisite for precisely characterizing the HTHP fluids (including compositional and volumetric properties), has been a vital challenge. The technique of fluid inclusion synthesis (FIS) in quartz is one of the only options. It has experienced an almost 40-year development since the standard fracture healing method was invented. Considerable advances in our understanding of physicochemical properties of geological fluids and their roles in many geological processes have been achieved by the use of the FIS techniques. A set of methodologies for fluid inclusion synthesis have been established. Great progresses have also been made, which includes the various pretreatment FIS techniques, the in situ fracturing FIS technique closely associated with the HTHP apparatus, the in situ fracturing refilled FIS technique for large fluid inclusion synthesis at controlled time under unfavorable conditions, and the novel fluid inclusion synthesis by fused silica capillary. Such great many progresses of the quartz FIS techniques have been scattered in the geochemists’ individual research work, and systematic collection and objective evaluation are missing. Consequently, we synthesize existing research, describe and identify the basic operations, discuss the methodological issues like pros and cons, and highlight the problems and prospects of the quartz FIS techniques. Furthermore, it is suggested that in situ and (or) large volume fluid inclusion synthesis will be an important future direction in view of the growing applications of the FIS techniques in combination with microanalytical techniques, especially the Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS). Our review would provide technical guidance to those who wish to investigate HTHP fluids and be beneficial to the future development and applications of the FIS techniques.

The sampling and phase characterisation of black mass

“Black mass” is the industry term used to describe a type of e-waste comprising crushed and shredded battery cells. It is an intermediate product in the recycling of spent, end-of-life, batteries. It comprises a mixture of metals including; lithium, manganese, cobalt and nickel, which are valuable recycling commodities, of increasing strategic and economic importance to meet future global demands in the “battery revolution”. The objective of this “phase characterisation” investigation was to provide an indicative profile of the morphological characteristics, grain size, composition and textural variability for a natural state (unprepared) and prepared (powdered) sample of black mass from Europe. It is envisaged that this is relevant to: (a) develop a pragmatic sampling strategy to ensure a non-biased, representative sample is provided for assaying; (b) determine the optimal processing route (e.g., hydrometallurgical, pyrometallurgical); (c) identify the presence of payable phases; (d) identify phases that may hinder metal recovery or penalty components; (e) develop assay procedures; and (f) assist in the identification of hazards and the mitigation of risks. The techniques used were: (1) visual examination and binocular microscopy; (2) manual scanning electron microscopy (SEM); (3) automated scanning electron microscopy with linked energy dispersive spectrometers (SEM-EDS), to characterise the phases present and particle types (using AMICS); (4) X-ray computed tomography (X-CT) to provide the 3D morphology of the particles; and (5) laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) to detect and quantify the phases that cannot be detected using automated SEM-EDS and X-CT. The results demonstrated that automated SEM-EDS can be used to characterise and quantify the phases present, and the phase chemistry allows the particle types to be assigned back to the primary battery components. Some phases identified are at present not linked back to the original components and further work is needed to refine the compositional groups, with the analysis of additional samples from different feeds/streams in Europe, China and USA. Interactive SEM-EDS analysis also demonstrated that there is a high-resolution chemical variability within the individual particle categories. X-CT imaging demonstrated the complex 3D textures and morphology of the particles, which is potentially significant during sample preparation and chemical analysis. Neither automated nor manual interactive analysis can determine the presence / abundance of the light elements, such as lithium. However, LA-ICP-MS was successful in detecting and quantifying lithium. Furthermore, LA-ICP-MS was able to determine contents of 67 other non-metals and metals at a 20-micron scale with ppm to ppb level detection limits.

Genesis of the Gaolong gold deposit in Northwest Guangxi Province, South China: Insights from in situ trace elements and sulfur isotopes of pyrite

The Guangxi-Yunnan-Guizhou district, also named Dian-Qian-Gui “Golden Triangle”, in Southwest China has a large amount of Carlin-type Au deposits. Gaolong is one source of Carlin-type Au deposit in the northwestern Guangxi Province. Pyrites are the major Au-bearing sulfides. Majority of Au are structurally bound Au+, with a few nanoparticles (Au0) occurring in the sulfides. In this study, in situ chemical and S isotopes of pyrites in the Gaolong Au deposit were analyzed by laser ablation inductively-coupled plasma mass spectrometry and laser ablation multi-collector inductively-coupled plasma mass spectrometry, respectively. Backscattered electron (BSE) images and chemical composition analysis showed that the pyrites were divided into four main types: (1) As-poor Py1 (pre-ore sedimentary or diagenetic stage, with prominent spotted and aggregate structures. These are fine-grained pyrite aggregates with rough surfaces and low brightness under the BSE, with edges often eroded by hydrothermal fluid); (2) As-weak Py2 (early ore stage, the core of the rim pyrite, with good crystallization and characteristic corrosion spots in the particle, and with the edge dissolved to show irregular structure); (3) As-rich Py3 (main ore stage, the narrow pyrite rims overgrowing Py1 and Py2, irregularly-shaped and less than 50 μm in width); and (4) As-rich Py4 (fine-grained pyrite, with good crystallization, high brightness, and symbiotic with Py3 and Py1, or an isolated distribution). Py1 contains higher concentrations of S, Fe, and W, and lower Co/Ni ratios (average of 0.91), suggesting a pre-ore origin. The ore-stage pyrites Py2, Py3, and Py4, have elevated mineralization elements—Au of 0.25–72 ppm, As of 2214–40613 ppm, Tl of 0.95–109 ppm, Sb of 31.16–1851 ppm, Cu of 49.09–910 ppm, with average Co/Ni ratios of 0.43. Au was positively correlated with As, Tl, Cu, and Ni in these pyrites. Electron micro probe analyzer (EMPA) elemental mappings show that: 1) Py1 has a low Au content, while Py2, Py3, and Py4 have high Au, As, Cu, Ti, and Mg contents; 2) Au occurs in As-rich pyrite in the form of invisible gold; 3) Rim pyrite contains high concentrations of Cu, which has a good positive correlation with As, while As and Au are decoupled on a smaller scale. The Au contents and Au/As ratios show that the Au-carrying fluids are unsaturated with Au. In situ S isotopes show that the δ34S values range from 10.19‰ to 13.79‰ with a mean value of 12.07‰ for Py1, 8.60‰ to 10.78‰ with a mean value of 9.77‰ for Py2, 1.42‰ to 8.29‰ with a mean value of 6.81‰ for Py3, and − 0.49‰ to 4.42‰ with a mean value of 1.67‰ for Py4. The δ34S data decreased from Py1 to Py4, whereas the As content increased significantly. This indicates that Au and As are enriched in ore-forming fluids, and the ore-forming fluids have low S isotope values. Based on a comprehensive study of geological and geochemical data, we believe that the magmatic hydrothermal genetic model can explain the genesis of the Gaolong gold deposit. We conclude that the S isotope of pyrites resulted from the mixing of magmatic S and sedimentary S, and the Au-bearing fluid came from deep-concealed granite, establishing a magma genesis of the Gaolong Au deposit.

Chemical study of group IIIF iron meteorites and the potentially related pallasites Zinder and Northwest Africa 1911

Group IIIF was established as a magmatic iron-meteorite group based on similar Ga and Ge abundances, unusually high Ga/Ge ratios, and the IIIAB-like interelement trends in its members; recent Mo and Ru isotopic data indicate that three of its members exhibit the isotopic signature of carbonaceous-chondrite (CC) irons. Here we report the elemental chemistry of this group and model its crystallization history. Included are new elemental data for IIIF irons acquired by both instrumental neutron activation analysis (INAA) and laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS). A fractional-crystallization model was used to evaluate the IIIF compositional trends for 19 elements and was unable to explain the observed fractionation trends for several key elements (Co, Ga, Ge). In particular, the inability of this model to match Co in the IIIF irons is striking because (1) group IIIF has the widest Co variation among all magmatic iron groups and (2) none of the tested initial S contents (0–20 wt.%) explains both the wide Co variation and steep Co-As slope. Attempts to fit subsets of the IIIF irons were also unsuccessful. In addition, group IIIF has the greatest variety of structural classes and kamacite bandwidths among all established magmatic iron groups. If the IIIF irons constitute a coherent group, they were derived from a parent body that experienced more complex processes than simple fractional crystallization of the core.The Zinder and Northwest Africa (NWA) 1911 pyroxene-bearing pallasites were recently suggested to be related to group IIIF based on their Ga and Ge contents, and we completed a petrographic study of the pallasite silicates and LA-ICP-MS analyses of their metal fractions. The two pallasites are related to one another: they have nearly identical mineralogical, elemental and O-isotopic compositions in their silicates and metals. Their metallic compositions resemble those of the IIIF irons Moonbi, St. Genevieve County, and Cerro del Inca, but their O-isotopic compositions resemble those of non-carbonaceous (NC) achondrites. Additional isotopic measurements are needed to test the potential genetic relationship to group IIIF.

Trace element geochemistry of sphalerite and chalcopyrite in arc-hosted VMS deposits

Trace element compositions of sphalerite and chalcopyrite have been investigated for four arc-hosted Cretaceous VMS deposits (María Teresa, Perubar, and Palma in Peru, and Cerro de Maimón in the Dominican Republic) using laser ablation inductively-coupled plasma mass spectrometry. In sphalerite, Fe, Mn, Cd, Hg, Ag, Sb, Se, In, Ge, and Ga are lattice-bound, whereas Sn, Tl, Bi, and Pb occur at least partly as mineral microinclusions. Significant variations in the contents of minor and trace elements are observed in sphalerite grains from individual deposits. A strong negative correlation between Fe (Inter-Quartile Range [IQR] 44,009–18,168 ppm) and Zn indicates a dominant Fe2+ ↔ Zn2+ simple isovalent substitution. Regarding potential high-tech by-products, the contents of In (IQR 42–1.6 ppm, up to 415 ppm) and Ga (IQR 31–5.9 ppm, up to 96 ppm) in the studied sphalerite are normally much higher than those of Ge (IQR 0.85–0.16 ppm, up to 9.3 ppm). Correlation trends suggest Cu+ + In3+ ↔ 2Zn2+, Cu+ + Ga3+ ↔ 2Zn2+, and more complex substitution mechanisms of Zn involving combinations of monovalent (Cu+, Ag+), divalent (Ge2+?), trivalent (In3+, Ga3+, [Sn3+?]), and quadrivalent (Ge4+, Sn4+) cations.As for chalcopyrite, Zn, Ag, Sn, Cd, Se, In, Ga, and Ge are interpreted to be lattice-bound, whereas Mo, Au, Tl, Sb, Pb, and Bi probably occur as microinclusions. Relative to sphalerite, chalcopyrite is depleted in In (IQR 28–8.4 ppm, up to 49 ppm) and Ga (IQR 8.3–2.9 ppm, up to 24 ppm) and enriched in Ge (IQR 5.9–0.70 ppm, up to 80 ppm). Of the other trace elements, Zn (IQR 426–190 ppm) is the most highly concentrated in the studied chalcopyrite, followed by Ag (IQR 136–23 ppm), Se (IQR 64–22 ppm), Sn (IQR 53–1.3 ppm), and Cd (IQR 12–6.0 ppm). General positive correlation trends between Zn, Cd, In, Ge, and Ga in chalcopyrite suggest varied coupled substitution mechanisms of Fe and Cu with fluctuating valences due to covalent bonding.Trace-element distribution patterns in sphalerite and chalcopyrite were studied for the zone-refined Sofía-D massive sulfide body in the María Teresa deposit, which comprises a lower lower portion of dominant pyrite sheathed upward by zones of chalcopyrite (Cu zone), sphalerite (Zn zone) and galena + sphalerite ± fahlore ± barite (Pb – Zn – Ag zone). Bottom to top of the sulfide body, sphalerite records progressive depletion in In, Cu, Mn, and Se, and enrichment in Ge. This distribution pattern agrees with increasing crystallization temperatures and/or volatile magmatic influx towards the lower portion of the massive mineralization. Distribution of trace elements in chalcopyrite is rather uneven except for a sustained enrichment in Se towards the basal portion of the sulfide body. The fact that such trends are preserved in spite of extensive recrystallization during thermal metamorphism in parts of the Sofía-D massive sulfide mineralization suggests i) a closed metamorphic system and ii) that element interdiffusion was prominently local. Accordingly, we propose that sphalerite lattice-bound trace elements distribution patterns described in this article can help determine the polarity of massive sulfide bodies in VMS districts in metamorphosed and tectonized terranes.

Translational Research of PT-112, a Clinical Agent in Advanced Phase I Development: Evident Bone Tropism, Synergy In Vitro with Bortezomib and Lenalidomide , and Potent Efficacy in the Vk*MYC Mouse Model of Multiple Myeloma

Introduction: PT-112 is a first-in-class platinum-pyrophosphate agent under advanced Phase I development in solid tumors. PT-112 was rationally designed to circumvent the toxicity and mechanisms of resistance associated with conventional chemotherapy. In previous preclinical models using PT-112, multiple cell signaling effects have been observed: p16 mediated G1/S cell cycle arrest; MDM2/p53 expression modulation; extrinsic apoptosis initiation; and signals indicative of immunogenic cell death (Ames et al., Eur. J. Cancer 2016). In addition, the ongoing first-in-human PT-112-101 Phase I trial in solid tumors has demonstrated a positive therapeutic index, with a range of biological activity observed at well-tolerated dose levels and a lack of severe hematotoxicity (Karp et al., J. Clin. Oncol. 2017).Due to the pyrophosphate present in PT-112, we hypothesized that PT-112 should localize to bone tissue, and be efficacious against bone marrow malignancies such as multiple myeloma (MM). Biodistribution was measured via laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS), along with translational experimentation in the orthotopic Vk*MYC mouse model of MM. In addition, an assessment of synergy was conducted in vitro in combination with standard of care (SoC) agents such as bortezomib (BOR) and lenalidomide (LEN).Methods: In vitro - Cell viability and IC50 values in MM1R and RPMI-8226 suspension cells were measured after treatment with PT-112, LEN, BOR, or PT-112-containing combinations thereof. Combination indices to assess synergy were calculated using the Chou-Talalay method.Biodistribution - After a single dose with 90 mg/kg PT-112 or vehicle control via tail vein injection, mice were euthanized 45min or 24h post-dose and snap frozen. Slides were prepared and LA-ICP-MS was used to measure and image the presence and concentration of platinum (Pt) in full sagittal plane cross sections, and in individual organs and tissues at higher spatial resolution.In vivo - Genetically engineered de novo Vk*MYC mice with established MM were treated with either 100 mg/kg PT-112 twice weekly (n=2) or 67 mg/kg (n=1) thrice weekly via intraperitoneal injection. In parallel experiments, mice engrafted with the BOR resistant Vk12598 transplantable line received vehicle (n=11) or PT-112 at 62.5 mg/kg (n=12) twice/week. M-spike levels were monitored weekly during treatment and for several weeks after.Results: In vitro, the combination of PT-112 with LEN and BOR resulted in strong synergy in both RPMI-8226 and dexamethasone-resistant MM1R multiple myeloma cells, as indicated by combination indices as low as 0.0029. In vivo, PT-112-derived Pt was observed in kidney, lung, liver and other tissue types, but most prominently in bone. All bone tissue observed had high concentrations of Pt, with the highest amount reaching ~15mM, a concentration >103 fold higher than the IC50 of PT-112 in in vitro cell viability experiments.PT-112 treatment induced a response in all of the de novo Vk*MYC mice with a >50% reductions in M-spike at the 2-week time point, passing the statistically correlated activity threshold indicative of robust activity in human MM patients (Chesi et al., Blood 2012). At this point treatments were discontinued, and M-spikes levels continued to decline for 1-2 weeks, with the lowest level observed at 19% of baseline at 11 days after treatment discontinuation. Importantly, we also noted pronounced single agent PT-112 activity against the BOR refractory Vk12598 tumors, resulting in statistically significant improved overall survival. In vivo combination studies are ongoing.Conclusions: Sophisticated biodistribution imaging techniques reveal the presence of PT-112 derived Pt in several target tissues, with a demonstrably preferential accumulation in bone tissue. These biodistribution results likely explain in part the strong efficacy observed in Vk*MYC mice. Given the predictive power of this model, the likelihood of PT-112 activity in human MM patients is high. Additionally, the potent synergy observed in in vitro systems provides encouraging evidence that PT-112 might combine well with SoC agents in treatment of MM. Taken together, these data provide a strong rationale for study of PT-112 as both a single agent and in combination in MM patients, with a further prospect for investigating other hematological malignancies. DisclosuresAmes:Phosplatin Therapeutics: Employment, Equity Ownership. Sharik:Phosplatin Therapeutics: Research Funding. Rather:Phosplatin Therapeutics: Research Funding. Hochart:Phosplatin Therapeutics: Research Funding. Bonnel:Phosplatin Therapeutics: Research Funding. Linehan:Phosplatin Therapeutics: Research Funding. Stauber:Phosplatin Therapeutics: Research Funding. Wing:Phosplatin Therapeutics: Employment, Equity Ownership. Jimeno:Phosplatin Therapeutics: Employment, Equity Ownership. Medina:Phosplatin Therapeutics: Research Funding. Bertino:Phosplatin Therapeutics: Research Funding. Chesi:Phosplatin Therapeutics: Research Funding. Bergsagel:Phosplatin Therapeutics: Research Funding.

Composite grains from volcanic terranes: Internal dose rates of supposed ‘potassium-rich’ feldspar grains used for optical dating at Liang Bua, Indonesia

In optical dating of feldspars, it is commonly supposed that potassium (K)-rich feldspar grains have been isolated for luminescence measurements by means of density separation. The K and rubidium (Rb) concentrations of these grains deliver a significant internal beta dose rate. K and Rb concentrations of 12.5 ± 0.5 wt% and 400 ± 100 ppm, respectively, are typically assumed for dose rate and age calculation, but this assumption may be wrong. Thorium (Th) and uranium (U) also contribute to the beta and alpha components of the internal dose rate. We investigated the K, Rb, Th and U concentrations of individual luminescent feldspar grains in four sediment samples from Liang Bua in Indonesia to determine single-grain internal dose rates and appropriate sample-average internal dose rates. The composition of the ‘K-rich’ feldspar fraction was investigated using X-ray diffraction spectrometry (XRD), which found that this fraction was heavily contaminated in each sample by quartz and plagioclase feldspars. Grains with detectable post-infrared infrared stimulated luminescence (pIRIR) signals were characterised using a range of techniques, including energy-dispersive spectroscopy (EDS), wavelength-dispersive spectroscopy (WDS) and quantitative evaluation of minerals using EDS (QEM-EDS). The grains were found to be composed of a range of minerals, including feldspars, quartz, clay minerals and heavy minerals, as well as volcanic glass. The K concentrations of these composite grains were determined using QEM-EDS, and their Rb, Th and U concentrations were determined using laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS). The calculated internal dose rates were very low for the majority of grains in each sample (<0.2 Gy.ka−1 for 180–212 μm-diameter grains), although a wide spread of internal dose rates was also observed. None of the samples showed any relationship between internal dose rate and either pIRIR signal intensity or equivalent dose (De). Two samples of clastic sediment were found to have different distributions of internal dose rate to those of two samples of tephra. To obtain reliable ages for sediment samples from Liang Bua thus requires the use of appropriate whole-of-grain and sample-average internal dose rates for grains with composite mineralogies deposited in these contrasting sedimentary contexts. More generally, greater consideration needs to be given to the internal dose rates of feldspar grains in volcanic regions such as Island Southeast Asia, especially composite grains with complex mineralogies, to ensure that the calculated ages are accurate.

Geochemistry and U-Pb ages from the Kösdağ Metavolcanics in the southern Central Pontides (Turkey): Complementary data for early Late Cretaceous island arc development in the Northern Neotethys

The Kosdag Metavolcanics (KMs) in the southern Central Pontides are exposed between the Izmir-Ankara-Erzincan Suture Belt in the south and the Sakarya Composite Terrane in the north. They comprise an approximately 40-km-long tectonic unit, bounded by the splays of the North Anatolian Transform Fault in the north and the Kizilca Thrust in the south. The basement of the unit mainly consists of metabasalts, metaandesites, and metarhyolites, with well-developed blastomylonitic textures, which are interlayered by recrystallized pelagic limestone and chert. Late Cretaceous pelagic limestones of the Dikmen Formation disconformably overlie the basement. Geochemically, the KMs exhibit enrichment in Th and La relative to Nb (and Ti), indicating subduction-related magmatic signatures. The KMs are subdivided into two main types, as Type 1 and Type 2, based on their relative Zr-Hf enrichment/depletion features. All of the members of the KMs have a subalkaline nature (Nb/Y - 0.08-0.19 for Type 1; Nb/Y = 0.05-0.13 for Type 2) and display a calc-alkaline affinity. The high Zr/Nb (38.1-52.9 for Type 1, 21.8-41.2 for Type 2), low Zr/Y (4.07-5.25 for Type 1, 1.58-2.44 for Type 2), and Nb/Y (0.08-0.14 for Type 1,0.05-0.10 for Type 2) signatures of the KMs indicate that they have derived from a depleted source, which has been modified by a subduction component. The laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) U-Pb zircon ages of the metarhyolite samples ranged between 94.64 +/- 0.77 Ma and 113.2 +/- 2.3 Ma, suggesting the presence of an intraoceanic subduction zone during the early Late Cretaceous within the Izmir-Ankara-Erzincan branch of the Neotethys Ocean in the Central Pontides.

LA-ICP-MS and MALDI-MS image registration for correlating nanomaterial biodistributions and their biochemical effects

Laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) imaging and matrix assisted laser desorption ionization mass spectrometry imaging (MALDI-MSI) are complementary methods that measure distributions of elements and biomolecules in tissue sections. Quantitative correlations of the information provided by these two imaging modalities requires that the datasets be registered in the same coordinate system, allowing for pixel-by-pixel comparisons. We describe here a computational workflow written in Python that accomplishes this registration, even for adjacent tissue sections, with accuracies within ±50 μm. The value of this registration process is demonstrated by correlating images of tissue sections from mice injected with gold nanomaterial drug delivery systems. Quantitative correlations of the nanomaterial delivery vehicle, as detected by LA-ICP-MS imaging, with biochemical changes, as detected by MALDI-MSI, provide deeper insight into how nanomaterial delivery systems influence lipid biochemistry in tissues. Moreover, the registration process allows the more precise images associated with LA-ICP-MS imaging to be leveraged to achieve improved segmentation in MALDI-MS images, resulting in the identification of lipids that are most associated with different sub-organ regions in tissues.

Five thousand years of bellyaches: Exploring boron concentration in ancient populations of the Atacama Desert.

This study explores whether ancient Atacama Desert populations in northern Chile were exposed to endemic boron contamination. Using Laser Ablation-Inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS), we studied 144 strands of ancient mummy hair, ranging from 3000 B.C. to 1500 A.D., excavated from the Lluta, Azapa, and Camarones valleys in northern Chile. We tested whether these ancient populations showed signs of significant boron concentration in hair tissue. On average, all individuals from these valleys showed high boron concentrations, ranging from 1.5 to 4 times above the average boron concentration in contemporary hair (baseline <0.85 μg/g). The boron concentration in mummy hair varied according to the main geographic areas mentioned above. The rivers of northern Chile have high geogenic boron concentrations. They contain 38 times above the recommended limit for human consumption. Geogenic boron contamination likely played a role in population morbidity and the types of crops that were cultivated in antiquity. The ancient populations were chronically affected by boron overexposure, suggesting that ancient geogenic water contamination should be considered when discussing the biocultural trajectories of ancient populations.

New horizons in quantitative compositional mapping – Analytical conditions and data reduction using XMapTools

Quantitative compositional mapping is a key technique for imaging solids and, therefore, for trying to understand compositional zoning systematics in a broad range of geological materials. Compositional mapping requires an adapted analytical method for efficient data collection, a post-processing calibration stage to obtain elemental concentration values, and specific computer tools for exploring and visualising the data. In this contribution, we describe optimal analytical conditions, possible physical limitations and data reduction strategies for compositional maps of major, minor and trace elements obtained by electron probe microanalysis (EPMA) and laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS). Data reduction is performed using the computer software XMapTools, which incorporates a large variety of options and tools for data processing, data calibration and data visualisation based on single and multi-channel maps or via binary, ternary and spider diagrams.

Dysregulated biodynamics in metabolic attractor systems precede the emergence of amyotrophic lateral sclerosis.

Evolutionarily conserved mechanisms maintain homeostasis of essential elements, and are believed to be highly time-variant. However, current approaches measure elemental biomarkers at a few discrete time-points, ignoring complex higher-order dynamical features. To study dynamical properties of elemental homeostasis, we apply laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) to tooth samples to generate 500 temporally sequential measurements of elemental concentrations from birth to 10 years. We applied dynamical system and Information Theory-based analyses to reveal the longest-known attractor system in mammalian biology underlying the metabolism of nutrient elements, and identify distinct and consistent transitions between stable and unstable states throughout development. Extending these dynamical features to disease prediction, we find that attractor topography of nutrient metabolism is altered in amyotrophic lateral sclerosis (ALS), as early as childhood, suggesting these pathways are involved in disease risk. Mechanistic analysis was undertaken in a transgenic mouse model of ALS, where we find similar marked disruptions in elemental attractor systems as in humans. Our results demonstrate the application of a phenomological analysis of dynamical systems underlying elemental metabolism, and emphasize the utility of these measures in characterizing risk of disease.

Melt and fluid evolution in an upper-crustal magma reservoir, preserved by inclusions in juvenile clasts from the Kos Plateau Tuff, Aegean Arc, Greece

Pre- to syn-eruptive fluids released by the magmatic system forming the non-welded rhyolitic Kos Plateau Tuff ignimbrite, Greece, were characterized using fluid inclusions entrapped in quartz from granitic clasts entrained from the roof or walls of the feeding magma reservoir. This fluid was initially of intermediate density and relatively low salinity (3–11 wt% NaClequivalent). Following significant pressure drop(s), it separated into immiscible brine and CO2-bearing vapor occurring as texturally less mature inclusions. The transition from single- to two-phase-fluid occurred at magmatic conditions, as supported by high fluid inclusion homogenization temperatures (ca. 700 °C) and simultaneous trapping of fluid inclusions with silicate melt inclusions. The large recorded pressure drop together with texturally immature fluid inclusion shapes suggests a possible direct relation between the fluid phase change and the incipient 161 ka caldera-forming eruption. All inclusion types occur predominantly along (pseudo-) secondary trails in the granitic clasts, indicating efficient entrapment in microfractures formed at high crystallinity, as attested to by elevated concentrations of incompatible elements in the silicate melt inclusions.Fast quenching of the inclusions due to eruption prevented significant post-entrapment chemical modification, providing pristine samples of magmatic fluid compositions. Element concentrations in co-existing fluids and silicate melt were analyzed using laser ablation inductively-coupled plasma mass spectrometry and compared in view of element transporting capabilities and magmatic-hydrothermal ore formation. Economically important metals such as Cu, Zn, Mo, and W were extracted from the silicate melt by the fluid. In particular, Cu concentrations in the single-phase fluid in the range of 100–500 ppm agree well with previous experimental and modeling studies and, therefore, represent values expected for primary magmatic fluids. Most elements got further enriched in the brine upon phase separation, except Li, B, and As, which may have contributed significantly also to the vapor phase. Considering the similarity between vapor and intermediate-density fluid in terms of salinity, however, the metal-enriched brine phase only comprised a minor fraction of the bulk fluid.