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Breast cancer (BC) is the leading cause of cancer death among women worldwide, making the discovery and quantification of new biomarkers essential for improving diagnostic and preventive strategies to limit dissemination and improve prognosis. Essential trace metals such as Fe, Cu, and Zn may play critical roles in the pathophysiology of both benign and malignant breast tumors. However, due to the high metabolic activity and reduced element selectivity of cancer cells, also non-essential elements may be taken up and may even be implicated with disease progression. This study investigates the spatial distribution and concentrations of both essential and non-essential elements in breast tissues, assessing their potential for diagnostic applications. Laser ablation (LA)–inductively coupled plasma–mass spectrometry (ICP-MS) with a time-of-flight (ToF) mass analyzer (LA-ICP-ToF–MS) was used to inquire the distribution of almost all elements across the periodic table and their abundance in metastatic (n = 11), non-metastatic (n = 7), and healthy (n = 4) breast tissues. Quantification was achieved using gelatine-based standards for external calibration to quantitatively map various elements. Overall, the Fe, Cu, Zn, Sr, and Ba levels were significantly increased in tumor samples with Sr and Ba showing strong correlation, likely due to their similar chemistry. Comparison of calibrated LA-ICP-ToF–MS data with a histologic staining demonstrated the possibility to clearly differentiate between various tissue types and structures in breast tissues such as tumor niche and stroma. The levels of the studied elements were significantly higher in the tumor niche areas compared to the stroma, and for Fe, a significant accumulation was observed in the tumor niche areas from the metastatic patient group relative to the levels found in the same areas of the non-metastatic group. LA-ICP-ToF–MS was used to quantitatively map the biodistribution of essential and non-essential elements in metastatic and non-metastatic breast cancer tissues. [ABSTRACT FROM AUTHOR]

The unconformity-related uranium (URU) deposits in the Proterozoic Athabasca Basin are one of the most important U resources in the world. This type of U deposit can be divided into monometallic (U) and polymetallic (U-Ni-Co-As) subtypes. While it is generally agreed that the URU deposits formed from reaction between oxidizing, basinal brines carrying U and/or Ni-Co-As with reducing basement fluids or lithologies, it is debatable whether the polymetallic deposits formed from co-enrichment of U-Ni-Co-As or enrichment of U superimposed by a separate Ni-Co-As mineralization event. This study addresses this problem through mineralogical, geochemical and fluid inclusion investigation of the Midwest U-Ni-Co-As deposit. Petrographic studies indicate that the sequence of ore precipitation started with uraninite, followed by Ni-Co arsenides and sulfoarsenides and then Cu-Pb-Fe sulfides, and this sequence was repeated episodically. This observation suggests that the deposit did not form from two separate U and Ni-Co-As mineralization events, but rather multiple episodes of U-Ni-Co-As mineralization. Linear correlations between chemical ages and Si-Ca-Fe contents of the most pristine uraninite U1 suggest a maximum primary mineralization of ca. 1600 Ma, which is consistent with the inferred primary U mineralization age in the Athabasca Basin. Microthermometric and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses of fluid inclusions in syn-mineralization drusy quartz indicate that the composition of the ore-forming fluids is characterized by the H2O-NaCl-CaCl2-KCl-MgCl2 system and comparable to those from both monometallic and polymetallic URU deposits. The relationship between U and Ni + Co in the fluid inclusions and its comparison with other URU deposits support a model in which U and Ni-Co were co-enriched in a unified mineralization process. The development of breccia structures in the ores and the dramatic fluid pressure fluctuation revealed by fluid inclusions suggest that the deposit formed from multiple episodes of fluid flow related to repeated reactivation of basement-rooted faults. [ABSTRACT FROM AUTHOR]

Chemical fingerprinting and spectrophotometry were combined to conduct a provenance analysis of radiolarite artefacts from three Moravian (Czech Republic) Aurignacian sites of Tvarožná I, Nová Dědina I and Milovice I. Of the different methods used, laser ablation with inductively coupled plasma mass spectrometry (LA-ICP-MS) was the best suited to distinguish the different areas containing radiolarite outcrops. Based on their chemical fingerprint, Moravian Aurignacian radiolarite artefacts were most likely imported from the western Slovak part of the Pieniny Klippen Belt. The abundant radiolarite outcrops in the Vienna region were apparently ignored, with the possible exception of two radiolarite artefacts from the Milovice I site. However, these could also have been manufactured from gravel radiolarites found around the site. Upon assigning other lithologies from Aurignacian sites in Moravia to their areas of provenience, it transpired those imports derived primarily from non-south-western regions. A similar situation was previously observed in the Moravian Szeletian, possibly indicating information exchange between the two Upper Palaeolithic cultures. Although the subsequent Gravettian culture relied more on long-distance imports, north-eastern − south-western movements and transfers were predominant up until the end of the Moravian Upper Palaeolithic, largely due to the communication corridor of the Moravian Gate. Upper Palaeolithic Moravia was an important source of raw materials and a hub for gathering other materials and information from concrete supply zones, while others were neglected. [ABSTRACT FROM AUTHOR]

Magmatic hydrothermal deposits are important sources of many bulk, precious, and rare metals, and have attracted interest from both academic and industrial communities. However, it is still unclear if the major enrichment of the ore-forming metals occurs in the parental magma source region, during the magma evolution, or after the fluid exsolution. Fluid inclusions trapped in hydrothermal minerals crystallized in the early, high-temperature stage before metal precipitation record information close to that of the initially exsolved magmatic fluids, which are helpful in revealing whether the metals have been already significantly enriched prior to the hydrothermal stage. In this study, available compositional data of such early-stage fluid inclusions from magmatic hydrothermal systems globally have been compiled. The results indicate that the concentrations of Cu, Sn, and W respectively from the Cu-, Sn-, and W-mineralized fluids are significantly higher than the hydrothermal systems that do not produce ores with the corresponding metals. This suggests that Cu, Sn, and W could have already been enriched in the magma source and/or magma evolution stage. The Mo concentrations show no difference between Mo-mineralized and Mobarren fluid systems, indicating no significant pre-enrichment in the source region or during the magma evolution. This also implies that an efficient collection of Mo from a large volume of magmas is required to account for the formation of a large Mo deposit. Almost all the hydrothermal fluids contain high concentrations of Fe and Zn-Pb, but only a few of them eventually form Fe or Zn-Pb deposits, reflecting an important role of the hydrothermal evolution process on the selective metal mineralization. The above results indicate that different metals are enriched in different stages of a magmatic hydrothermal system, and that the major roles played in the formation of a deposit vary with the metal types. In addition to the metal concentrations in the ore-related magmas and fluids, other factors (including but not limited to the intrusion shapes, emplacement depths, structural pathways, and wallrock properties) are also critical in determining the fertility and mineralization diversity of a magmatic hydrothermal system. [ABSTRACT FROM AUTHOR]

The Muzidian gneiss complex (MGC) in the Northern Dabie Orogen is the oldest exposed rock formation in the South China block. However, there is still a lack of research on its metamorphic age and tectonic implications. LA-ICP-MS in situ U-Pb dating and trace element analysis of monazite were carried out on two gneiss samples from the MGC. The results show that most monazite grains exhibit homogeneous features with no zoning, evident depletion of HREEs and negative Eu anomalies, suggesting that they may be of metamorphic origin. The monazite U-Pb ages of the two gneiss samples are 129±1Ma and 130±1Ma, respectively, which represent the time of metamorphism of the MGC. These ages are broadly consistent with the emplacement age of the early Cretaceous granitoids in the Muzidian area, as well as the large amount of exposed migmatites in the Northern Dabie Orogen. Our study shows that the extensional collapse of the thickened continental crust and the delamination of the orogenic crustal root during the early Cretaceous of the Dabie Orogen caused contemporaneous metamorphism, migmatation, and magmatism, which constrained the tectonic regime switch time of the Northern Dabie Orogen from compression to extension to ~130Ma. [ABSTRACT FROM AUTHOR]

The tea-dust glaze ancient porcelain is one of the earliest crystalline glazes, which is rarely studied deeply because of its rarity. In this study, the mineral crystals in tea-dust glaze made in the Ding Kiln of the Northern Song Dynasty were analyzed by optical microscope (OM), laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), scanning electron microscopy coupled with an X-ray energy dispersive spectrometer (SEM-EDS), laser confocal Raman spectrometer (LRS), and high-resolution time of flight-secondary ion mass spectrometry (ToF-SIMS). The results show that the main crystal phase in the glaze is the same as that of the Longquanwu Kiln in the Liao and Jin Dynasty, which is anorthite and augite. The overall performance of the glaze is that the sauce-black glaze matrix is rich in iron (Fe2O3 mean 9.73%) and the mineral crystal is rich in iron (Fe2O3 mean 11.33%). In addition to α-Fe2O3 crystals, Fe3O4 crystals and other recrystallized minerals after melting, the glaze also has pleonaste, residual kaolinite and other unmelted minerals from raw glaze materials. The residual kaolinite shows that the firing temperature of the samples in this study was most likely below 1200℃. [ABSTRACT FROM AUTHOR]

Eclogite‐facies rocks provide important constraints on the behaviour of convergent plate boundaries and the geometries of tectonic reconstructions due to the high to ultrahigh pressure conditions at which they form. Many eclogite occurrences are documented near the suture zone of active collisional settings where they are interpreted to mark the approximate location of former ocean basin subduction. Such observations influence tectonic interpretations for older eclogites within more deeply eroded and/or less well‐exposed terranes. The eclogitic Glenelg inlier in northwest Scotland is one such example, with c. 1 Ga eclogites having previously been interpreted as marking the trace of a Grenville‐aged collisional suture zone that defines a third 'arm' to the Grenville orogen alongside well‐defined sutures in North America and Scandinavia. Here we use a combination of geochronology, phase equilibrium modelling and accessory‐phase thermometry to show that the eclogite‐facies assemblages were produced at ∼$$ \sim $$18–19 kbar and 700°C–750°C from c. 1.1 to 1.0 Ga. Accounting for the foreland basin setting of equivalent‐aged sedimentary rocks in the region and demonstrating the thermal viability of this setting, we show that eclogite formation occurred in deforming foreland crust adjacent to the Grenville orogen, in a setting broadly analogous to fault‐bounded basement uplifts in the forelands of active deformation belts, such as the Himalayas and Andes. Our results demonstrate that eclogite‐facies rocks can form in a greater range of tectonic settings than are sometimes considered, with implications for tectonic reconstructions of collisional zones. In this instance, our results remove the need for a third 'arm' of the Grenville orogen by placing Glenelg in a foreland setting, reconciling the absence of plentiful Grenville‐aged metamorphic rocks in northwest Scotland, the sedimentological record and paleomagnetic data in the wider region. [ABSTRACT FROM AUTHOR]

Trace element analysis of otoliths from core to edge was used to reveal differences in habitats of larvae and early juveniles of Japanese jack mackerel (Trachurus japonicus) caught in the East China Sea (ECS), Pacific Ocean, and Sea of Japan. Multi‐element signatures (Sr:Ca, Mg:Ca, Na:Ca, K:Ca, and Ba:Ca) were analyzed with multivariate statistics to determine whether these element signatures provide insight into regional population structure. The median values of elements: Ca ratios in otolith core region differed significantly among areas, with most elements between the ECS and the Pacific Ocean or Sea of Japan showing significant differences. The Sr:Ca ratios exhibited a V‐shaped trend from the otolith core to the edge, which was likely related to the vertical habitat layer shift of larvae and early juveniles of T. japonicus. Canonical analysis of principal coordinates using the element: Ca ratios and the hatching day were re‐classified according to the sampling area with higher accuracy in the ECS (88–95%) and the Sea of Japan (76–83%) compared to the Pacific Ocean (69–72%). These results indicate that the proportion of eggs, larvae, and early juveniles transported by the Kuroshio Current from the southern ECS—the main spawning ground—to the Pacific Ocean or the Sea of Japan is low and that juveniles distributed in the coastal waters off southwestern Japan may have originated from local spawners. These results suggest that determining the elemental composition of larvae and juveniles of T. japonicus is effective in determining the habitat differences of this species in the three regions. These findings will help to understand population structure and recruitment process of this species around Japan. [ABSTRACT FROM AUTHOR]

Discovered within the North Himalayan Metallogenic Belt (NHMB), the Zhaxikang Pb–Zn–Ag–Sb deposit stands as the sole super-large scale ore deposit in the region. This deposit holds significant quantities of Pb and Zn (2.066 million tons at 6.38% average grade), Ag (2661 tons at an average of 101.64 g/t), and Sb (0.235 million tons at 1.14% average grade), making it one of China's foremost Sb–polymetallic deposits. Stibnite represents the main carrier of Sb in this deposit and has been of great attention since its initial discovery. However, the trace element composition of stibnite in the Zhaxikang deposit has not yet been determined. This study carried out an analysis of the distribution patterns and substitution processes of trace elements within stibnite gathered from the Zhaxikang deposit, aiming to provide crucial information on ore-forming processes. Utilizing high-precision laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), we discovered that the studied stibnite is notably enriched in arsenic (~100 ppm) and lead (~10 ppm). Furthermore, the notably consistent time-resolved profiles suggest that elements such as Fe, Cu, As, In, Sn, Hg, and Pb predominantly exist as solid solutions within stibnite. Consequently, it is probable that the enrichment of Cu, Pb, and Sn in stibnite is due to isomorphic substitution reactions, including 3Pb2+↔2Sb3+, Cu+ + Pb2+↔Sb3+, and In3+ + Sn3+↔2Sb3+. Apart from that, Mn, Pb, and Hg with the spiky signals indicate their existence within stibnite as micro-inclusions. Overall, we found that the trace element substitutions in stibnite from the Zhaxikang Pb–Zn–Ag–Sb deposit are complicated. Incorporations of trace elements such as Pb, Cu, and In into stibnite are largely influenced by a variety of factors. The simple lattice structure and constant trace elements in studied stibnite indicate a low-temperature hydrothermal system and a relatively stable process for stibnite formation. [ABSTRACT FROM AUTHOR]

The conducted study shows that apatite is one of the key accessory minerals in the ultramafic-mafic rocks of the Khudolaz differentiated complex in the Southern Urals, including late pegmatoid gabbro. Petrographic and mineralogical investigations determine apatite crystallizing simultaneously with hornblende in pegmatoid gabbro from the residual water-saturated melt after plagioclase crystallization at a temperature of 990–800 °C, a pressure of 1–3 kbar, oxygen fugacity from −13.9 to −10.7, and water content of 3.9–5.5 wt. %. Pegmatoid gabbro apatite (Appg) from the Severnyi Buskun composite massif differs from early ultramafic-mafic apatite having a fairly high potential for sulfide-platinum metal mineralization in low chlorine and high fluorine content. Low sulfur concentrations in Appg testify to the lack of sulfide-platinum metal mineralization potential of pegmatoid gabbro, but a scanty potential for rare-metal mineralization (e.g., REE) is possible. Appg is quite poor in REE despite the enrichment of pegmatoid gabbros in REE relative to early ultramafic-mafics, which indicates REE accumulation in the fluid. The ratios of cerium and europium anomalies characterize the Appg crystallization under conditions transitional from the magmatic to the hydrothermal stage. Generally, apatite is a good indicator of the difference in the conditions of formation of late pegmatoid gabbro and early ultramafic-mafic rocks, which determines the importance of this mineral in mineralogical and petrological studies. [ABSTRACT FROM AUTHOR]

The effects of different regional tectonic events on the Neoproterozoic basement rocks of the Arabian–Nubian Shield in Sinai, as well as the Egyptian unstable and stable shelves, remain uncertain. Coupling fission-track thermochronometry findings with the modeling of the time–temperature history has proved to be an effective method for tackling these issues. The obtained zircon fission-track ages were differentiated into two groups from the Ediacaran–Cambrian and the Ordovician–Carboniferous periods, while the apatite fission-track data revealed two separate groups of cooling ages of the Carboniferous–Triassic and Late Cretaceous ages. The integration of these cooling ages and modeling of the time–temperature history revealed four discrete cooling pulses during the Neoproterozoic, Devonian–Carboniferous, Cretaceous, and Oligocene–Miocene eras. After integrating our findings with the regional tectonic historical and sedimentological records, these could be identified as cooling/exhumation pulses activated in response to the post-accretional event of erosion, Variscan tectonism, the disintegration of Gondwana, and the Gulf of Suez rifting, respectively. Furthermore, the southern border of the Egyptian unstable shelf was found to extend southward to South Sinai and south of the Bahariya depression. [ABSTRACT FROM AUTHOR]

Garnet U‐Pb dating by laser ablation‐inductively coupled plasma‐mass spectrometry requires the development of matrix‐matched reference materials of variable chemistry and U mass fraction for accurate analysis. Additional calibration of existing primary reference materials is also justified based on the relatively poor calibration of some of the widely available primary reference materials that are currently utilised by the geoscience community. We present a micro sampling workflow combined with a refined ID‐TIMS methodology for the generation of high precision (~ 0.1%) U‐Pb dates from domains within garnet single crystals. Using this workflow, we calibrated two new natural andradite reference materials, the Jumbo andradite (And99; 110.34 ± 0.03 (0.04) [0.13] Ma, n = 7, MSWD = 1.21) and the Tiptop andradite (And87; 209.57 ± 0.11 (0.13) [0.26] Ma, n = 6, MSWD = 1.39). We also present additional calibration of the widely utilised Willsboro‐Lewis andradite primary reference material (And90; 1024.7 ± 9.5 (9.6) [9.6] Ma (2s; overdispersed), n = 6). Wafers of the Jumbo and Tiptop andradite reference materials are available from the authors upon request. [ABSTRACT FROM AUTHOR]

Baddeleyite is an important U‐Pb geochronometer and Hf isotope tracer that commonly occurs as an accessory phase in silica‐undersaturated igneous rocks of terrestrial and extra‐terrestrial origin. Currently, very few well‐characterised, large sized reference materials are available for baddeleyite U‐Pb geochronology and Hf isotope measurement. In this study, we document a baddeleyite reference material (SK10‐3) of Cenozoic age. SK10‐3 is inclusion‐free and does not contain secondary alteration minerals. The baddeleyite has uniform U‐Pb ages and Hf isotope ratios, within analytical uncertainty, as demonstrated by multiple LA‐ICP‐MS spot analyses (weighted mean 206Pb/238U age: 31.59 ± 0.11 Ma, MSWD = 0.7, n = 197) and LA‐MC‐ICP‐MS analyses (arithmetic mean 176Hf/177Hf ratio: 0.282741 ± 59, 2s, n = 188). Seven ID‐TIMS analyses yielded a weighted mean 206Pb/238U age of 31.592 ± 0.020/0.022/0.040 Ma (n = 7, 2s, MSWD = 2.2). Nine aliquots of MC‐ICP‐MS analyses yielded an arithmetic mean 176Hf/177Hf ratio of 0.282742 ± 8 (2s). We further demonstrate that the method of shallow‐pit (~ 2 μm depth) ablation substantially improves the precision and accuracy of baddeleyite U‐Pb ages. SK10‐3 has a relatively high 176Yb/177Hf ratio (~ 0.007) compared with most other baddeleyites, allowing the precise measurement of βYb and may be useful in generating the βYb‐βHf relationship during LA‐MC‐ICP‐MS Hf isotope measurement. SK10‐3 may be a useful addition to previously distributed baddeleyite reference materials for microbeam‐based U‐Pb geochronology and Hf isotope measurements. [ABSTRACT FROM AUTHOR]

In this contribution, we document changes in detrital zircon ages in the upper Devonian (Famennian) to lower Carboniferous (Mississippian) Billefjorden Group on Bjørnøya, the southernmost island of Svalbard. This alluvial, coal‐bearing clastic succession is widely distributed across the archipelago and the Barents Shelf. The sediments were deposited in subsidence‐induced lowlands that formed just after regional post‐Caledonian collapse‐related extension, which created the classical 'Old Red Sandstone' basins during the Devonian, and prior to localised rift‐basin development in the middle Carboniferous (Serpukhovian–Moscovian). Moreover, the succession is little affected by Ellesmerian compressional deformation, which occurred in the latest Devonian. However, little is known of the provenance and regional sediment routing in this tectonically transitional period between the post‐Caledonian structuring events in the Devonian and the middle Carboniferous rifting. It has previously been invoked that a regional fault running parallel to the western Barents Shelf margin, the West Bjørnøya Fault, controlled sedimentation in the area. Here, we combine detrital zircon U–Pb ages and sedimentological data to investigate stratigraphic provenance variations and test whether tectonics controlled deposition of the Billefjorden Group on Bjørnøya. Sedimentological investigations demonstrate changes in fluvial style with intercalations between successions dominated by meandering channel fills and abundant overbank fines to sandstone‐dominated sheet‐like successions of braided stream origin. Palaeocurrent data show that two competing drainage directions accompany the changes in fluvial architecture. Northeasterly transport directions, recorded in the braided stream deposits, indicate possible fault‐transverse drainage. The detrital zircon content in these deposits indicates sourcing from Caledonian terranes in Northeast Greenland. Northwest‐oriented transport directions, measured in the meandering channel deposits, are inferred to represent axially positioned drainage systems. These may have been sourced from either Northeast Greenland, a more localised source, or Baltica. The latter would require long‐distance sourcing, which, given the tectonic setting of the region, seems unlikely. Although our sedimentological observations point to syn‐tectonic deposition, this is not clearly captured in the detrital zircon data, suggesting a common source for the Late Devonian–Mississippian fluvial systems of Bjørnøya. Thus, combined with previously published provenance data from Svalbard and Greenland, we demonstrate that the East Greenland Caledonides formed a long‐lived and significant source area which provided sediments to nearby basins from the Devonian to the Early Cretaceous. [ABSTRACT FROM AUTHOR]

Yechangping super-large porphyry-skarn type Mo-W deposit, located in the East Qinling Mo polymetallic metallogenic belt, preserves crucial information on skarn formation evolution and mineralization. Through detailed field geological surveys and microscopic identification, magnetite in Yechangping Mo-W Deposit is classified into 3 types:Mt1 magnetite, formed during the late skarn stage, clay minerals, etc.; Mt2 magnetite, formed during the oxide stage, is semi-euhedral to euhedral and associated with garnet, tremolite, actinolite, etc.; and Mt3 magnetite, densely disseminated and associated with molybdenite or occurring in quartz polymetallic sulfide veins. Electron probe and LA-ICP-MS in-situ trace element analysis show that the average FeO content increases progressively from Mt1 to Mt3 magnetite. Mt1 magnetite is rich in elements such as Si, Mg, and Na, and has the highest content of V, Cr, Ti, Al, and Mo. Ti content in Mt2 magnetite decreases significantly, with a slight reduction in Si content and the highest levels of Mg and Mn. Mt3 magnetite has the lowest content of Ti, Si, Na, and Ca. The changes in magnetite element characteristics suggest that Fe is easily replaced by Si, Ca, and Al elements, with Mo and other ore-forming elements gradually enriching in the ore-forming fluids during magnetite crystallization. Genesis discrimination diagrams of magnetite indicate that Mt1 magnetite has a different source material compared to Mt2 and Mt3, tending more toward a magmatic-hydrothermal origin, while Mt2 and Mt3 are more metamorphic hydrothermal in nature. The host wall rock participated more in the mineralization with the formation of Mt2 magnetite. From the higher temperature early Mt1 magnetite to the lower temperature late Mt3 magnetite, V and Ti show a clear positive correlation. Discrimination diagrams for fluid-rock interaction indicate that metasomatism intensifies progressively. Therefore, changes in oxygen fugacity and the increasing degree of fluid-rock interaction in Yechangping Mo-W Deposit are the main factors controlling mineralization. [ABSTRACT FROM AUTHOR]

Azurite, a historical blue mineral pigment, has previously been described to contain certain elemental impurities. These may originate from host rocks, vein fillings, or the primary copper ore mineralization. In this study, azurites (and also green malachites) from three important Central European deposits with a potential of being exploited for pigment usage already in the Middle Ages have been studied, together with azurite from Chessy, France, with a different geological setting. Using electron probe microanalysis and, more importantly, laser ablation inductively coupled plasma mass spectroscopy for trace elemental analysis, several indicators were pinpointed as important for provenance: characteristic elemental fingerprint of the deposit, e.g., elevated lead (Pb) in combination with rare earth elements, may be combined with zinc (Zn)/arsenic (As) ratio (indicating sources of excess Zn in the primary deposit) and the overall amount of metal impurities (suggesting the source mineral of copper for azurite formation). In addition, malachites from the same deposits were found to preferentially incorporate primary ore metal elements as well as Cd, Mg, Mn, or U. Therefore, if azurite pigment contains an elevated amount of malachite as an impurity, it may significantly influence the overall elemental composition. The results obtained on geological samples were applied to two micro-samples of works of art containing azurite-rich layers originating from the 13th–14th and 16th centuries. It was shown that it is highly beneficial to focus on the overall trace elemental composition of the paint layer and not on the admixed mineral grains, as their presence, especially in minute micro-samples, is largely accidental and thus not representative. Although a higher number of samples need to be studied in the future, the newly described criteria made it possible to exclude some of the localities of the employed azurite pigment. This confirmed the key importance of trace elements analysis of mineral pigments for the provenance studies of fine arts. [ABSTRACT FROM AUTHOR]

Glass beads from two Islamic archaeological sites in the Tagus valley in central Spain were selected and analysed by laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS), and a subset of samples (n = 6) was analysed for Pb isotopes by multicollector thermal ionization mass spectrometry (MC‐TIMS). The analytical and isotopic data of the beads from Ciudad de Vascos (Toledo) and Albalat (Cáceres) demonstrate beyond reasonable doubt that glass beads were produced in the Iberian Peninsula during the Islamic period using local Pb‐silica and soda‐rich plant‐ash glass. The bead workshops in al‐Andalus were evidently part of an efficient system of glass collection and recycling, and used only relatively simple bead‐making techniques such as winding and folding. At present it is unclear to what extent the Islamic bead‐makers in the Iberian Peninsula were involved in the international trade in glass beads or whether their products were mainly destined for a regional market. Despite local production, some samples show compositional and typological features that suggest the import of finished glass beads, perhaps from Central Asia. [ABSTRACT FROM AUTHOR]

The Xianghualing large tin-polymetallic skarn deposit is located in the Nanling W-Sn metallogenic belt, South China, showing distinct spatial zoning of mineralization. From the contact between granite and carbonate rocks, the mineralization transitions from proximal skarn Sn ore to cassiterite-sulfide ore and more distal Pb–Zn-sulfide ore. This study reveals the fluid evolution and genetic links among these different ore types. The physical and chemical characteristics of fluid inclusions from each ore types indicate that the skarn Sn ore, cassiterite-sulfide ore, and Pb–Zn-sulfide ore all originated from the identical magmatic fluid exsolved from the Laiziling granite. Their formation, however, is controlled by diverse fluid evolutionary processes and host rock characteristics. The Sn–Pb-Zn-rich fluids were primarily derived from cooled and diluted magmatic brine, which is generated by boiling of initial single phase magmatic fluid. Mixing of magmatic brine with meteoric water is crucial to form skarn Sn ore. Redox reactions of aqueous Sn (II) complexes with As (III) species and/or minor CO2 during short cooling period of ore-forming fluid is likely an effective mechanism to form high-grade cassiterite-sulfide ores, accompanied by favorable pH conditions maintained through interaction with carbonate host rocks. The later stage addition of meteoric water prompts the formation of Pb–Zn-sulfide ore. Comparing these findings with the characteristics of initial or pre-ore magmatic fluids in both mineralized and barren granitic systems indicates that high Sn content in the pre-ore fluids and the suitable fractional crystallization degree of the parent magma may determine high Sn mineralization potential in granitic magmatic-hydrothermal systems. [ABSTRACT FROM AUTHOR]

Porphyry-epithermal veins hosting Re-rich molybdenite and rheniite (ReS2) from the Maronia Cu-Mo ± Re ± Au porphyry in Thrace, NE Greece, provide new insights into the hydrothermal processes causing extreme Re enrichment. Quartz trace element chemistry (Al/Ti, Ge/Ti), Ti-in-quartz thermometry, and cathodoluminescence imaging reveal multiple quartz generations in consecutive hydrothermal quartz-sulfide veins associated with potassic, sericitic, and argillic alteration. Fluid inclusions in different quartz generations indicate that phase separation and fluid cooling are the main ore-forming processes in the porphyry stage (~ 500 – 350 °C), whereas mixing of a vapor-rich fluid with metalliferous (e.g., Pb, Zn, Au) meteoric water forms the epithermal veins (~ 280 °C). These processes are recorded by trace element ratios in pyrite that are sensitive to changes in fluid temperature (Se/Te), fluid salinity (As/Sb, Co/As), and mixing between fluids of magmatic and meteoric origin (Se/Ge). Highly variable intra-grain δ34S values in pyrite record S isotope fractionation during SO2 disproportionation and phase separation, emphasizing the importance of in situ δ34S analysis to unravel ore-forming processes. High δ34S (~ 4.5‰) values of sulfides are indicative of low SO42−/H2S fluid ratios buffered by the local host rocks and mixing of the magma-derived fluid with meteoric water. The formation of Re-rich molybdenite (~ 6600 ppm) is favored by cooling and reduction of a magma-derived, high-temperature (~400 °C), oxidized, and Re-rich fluid triggering efficient Re precipitation in early veins in the potassic alteration zone. The systematic temporal fluid evolution therefore reveals that coeval cooling and reduction of oxidized Re-rich fluids cause extreme Re enrichment at the Maronia porphyry system. [ABSTRACT FROM AUTHOR]

Porphyry indicator zircons (PIZ) are often used as an exploratory guide to distinguish fertile granitoid-hosted porphyry copper deposits (PCD). Alumina-saturated granitoids with higher zirconium (> 200 ppm) contents are often the hosts of PCD. REE profiling of zircon is used here to evaluate the chemistry of zircon from a blend of I- and A-type granitoids that hosts the 'Kaziranga' porphyry copper mineralization in the Karbi Hills of the Shillong Plateau. Zircon Hf(t) (1.69–9.88; av.4.65) and whole rock 87Sr/86Sr (0.703) of the Kaziranga granitoids suggest magma derivation in an intraplate or primitive island arc tectonic setting, in which the active mechanism of magma derivation was partial melting of a metasomatically enriched lithospheric mantle that was probably fertilized by an intraplate mantle plume. The fertility indicators with PIZ are grouped with respect to the distribution pattern of normalized REEs, as they exhibit low LREE and enriched HREE, large + Ce, and small -Eu anomalies. The hypogene alteration zones have developed on a regular basis, the potassic alteration zone being close to the central zone around Kuthori in the north Karbi Hills. Although the hosts demonstrate expansion and development of the hypogene alteration zones, the zircons from the mineralized granitoids of Kuthori central zone and granitoids of the nearby Panbari–Dallamara shear zone have similar REE pattern. The target zone's zircon has higher values of ΣHREE, U, Th, Y, Nb, and Hf. The admissible range of fertile PCD is matched by the cross plots of critical element ratios, demonstrating high calculated Ti in zircon temperature (up to 828 °C). [ABSTRACT FROM AUTHOR]

Determining the provenience of archaeological objects relies on the so-called “provenience postulate,” namely, that sources of these objects are more compositionally distinct from each other than they are internally variable. For ceramics, it can be relatively straightforward in geologically heterogeneous environments to determine where vessels were produced, and whether they were traded or not. In geologically homogeneous regions, this can be far more complicated. In this study, we mineralogically and chemically compare Bronze Age ceramics (primarily Middle Bronze Age) from five archaeological sites on the Great Hungarian Plain to a large regional clay sample. The Great Hungarian Plain is comprised almost entirely of Pleistocene loess deposits, yet prior compositional studies have identified patterned variability between ceramics from different sites. Our results show that chemical variation in the region is continuous and clinal, making it difficult to strictly apply the provenience postulate to identify distinct production locations. However, we show that this clinal chemical variability can be used to make broad statements about whether most ceramics at any given site were produced relatively locally or were obtained from further distances (c. 50 km or more). We show that while production at most of our study sites was likely relatively localized, in one instance (the tell at Berettyóújfalu-Herpály-Földvár), many ceramics may have been obtained from other Bronze Age communities, including those in the Körös River drainage. [ABSTRACT FROM AUTHOR]

The Gulf of Suez is a continental rift basin that has been developed during the Oligocene-Miocene as a northern extension of the Red Sea rift system. The Oligo-Miocene rift-activated flanks are represented by exposures of the Neoproterozoic basement rocks of the Arabian-Nubian Shield. An additional thermal overprint (i.e. mantle plume) and the preceding tectono-thermal events that also affected the rifting dynamics and the uplift of its flanks remain uncertain. We here present thermochronological data for 20 basement samples collected from the Gabal Somr ElQaa area at the northwestern flank of the Gulf of Suez. The resulted zircon fission-track ages could be divided temporospatially into two groups: the Cambrian and the Silurian-Devonian with average ages of 503 ± 14 Ma and 407 ± 11 Ma, respectively. While apatite fission-track data reveal three different age groups of the Devonian-Carboniferous, the Permian-Triassic, and the Late Cretaceous, with average ages of 349 ± 10 Ma, 246 ± 6 Ma, and 81 ± 5 Ma, respectively. The modelled t-T histories indicate four cooling pulses during the Neoproterozoic, the Devonian-Carboniferous, the Cretaceous, and the Oligocene-Miocene. Integrating our findings with the regional tectonism and depositional records indicates that these cooling pulses could be attributed to synchronous activities of the post-accretion erosional event, the Variscan tectonic event, the Mid-Atlantic Ridge spreading, and the Gulf of Suez rifting. The Gulf of Suez is a passive rift, formed by a single and rapid rifting pulse within the framework of the Red Sea rift system. An additional east-southward far-field thermal overprint from the Arabian marginal plume partially affected the Suez rifting process. This thermal print affected only the rift’s southern portion of its eastern flank, causing syn-rift cooling ages, highly elevated rift flanks, and an increased heat flow. The western rift flank and the northern segment of the eastern flank are characterized by pre-rift cooling ages, modest rift flanks, and reduction in heat flow. [ABSTRACT FROM AUTHOR]

Glass beads first appear in the archaeological record of southern Africa around the mid-first millennium CE, marking the earliest signatures of extensive connections between the southern African region, the East African coast, and the broader Indian Ocean rim. Key research focused on glass beads, particularly from notable southern African polities, like the renowned Mapungubwe and Great Zimbabwe sites, has laid the groundwork for a regional taxonomic series of these beads, emphasizing their role as indicators of wealth and social status. This paper introduces new data on 59 glass beads from a recently excavated and lesser-known Zimbabwe culture site in the Mberengwa region of south-central Zimbabwe. The analysis employs non-invasive techniques, including typological classification and laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS). The investigation identifies six glass bead series from Chumnungwa, composed of plant ash-lime (v-Na-Ca), vegetable soda-high alumina (v-Na-Al), and soda-based glasses with high-alumina concentrations (m-Na-Al). These beads, widely distributed in Asia and Africa between the eight and seventeenth centuries, shed new light on the geochemistry, provenance, and circulation patterns of glass beads in southern Africa, particularly within a community situated beyond the well-known Iron Age polities. Notably, Chumnungwa emerges as the first known Zimbabwe culture site in southern Africa to yield m-Na-Al 6 glass beads. However, as recently demonstrated at the Toutswe sites in Botswana, it is probable that other Zimbabwe culture sites in the region also possessed m-Na-Al 6 glass beads. These beads may have been misclassified as m-Na-Al 2 glass since this group was only recently unveiled on the East African coast, after the bulk of the currently available literature had been published. Insights drawn from contextual recovery data and Shona anthropology form the basis for an extended discussion on the consumption and sociality of glass beads in Iron Age southern Africa. Ultimately, the study underscores the challenge of typologically categorizing beads into established series without the application of LA-ICP-MS and other scientific approaches. [ABSTRACT FROM AUTHOR]

A series of three CGSP‐P phosphate matrix reference materials, with variable element mass fractions, were synthesised by co‐precipitation with CaCl2 and (NH4)3PO4 to form a hydroxylapatite matrix. Each powder sample was packaged into multiple bottles and pressed into tablets as replicates. The within‐bottle homogeneity was evaluated by the repeatability of element mass fractions of six spots in per tablet of CGSP‐Ps by LA‐ICP‐MS. For the between‐bottle homogeneity evaluation, one approach adopted the % RSD of element mass fractions in twelve different tablets from twelve bottles in the same reference material in comparison with the repeatability field of LA‐ICP‐MS analyses obtained from homogeneous glasses, and the other used a one‐way analysis of variance (ANOVA) approach. Most of the elements (e.g., Mg, Ca, P, Mn and REE) were homogenous within 10% RSD, and other elements (e.g., Si, Al, K, Rb, Cs and Ni) were considered heterogeneous (with > 20% RSD). All of the elements passed the t‐test except Ni in CGSP‐P3, and V, Cr, Ni, Zr, Gd, Dy and Th in CGSP‐P4 after a 29‐month period stability examination by LA‐ICP‐MS. The preliminary reference values and standard uncertainties for CGSP‐Ps are given with a network of methods and eight laboratories by bulk analysis according to ISO Guide 35:2006 and JJF 1343‐2012. [ABSTRACT FROM AUTHOR]

In marine fishes of commercial interest, defining habitat use and migration strategies through ontogeny can help better understand the structure and dynamics of harvested populations and guide their management. The present study relied on otolith chemistry to identify three contingents within the Atlantic halibut (Hippoglossus hippoglossus) stock in the Gulf of St. Lawrence (GSL). We differentiated two chemical signatures from otolith edges, one for shallow (<100 m) and another one for deep (>100 m) waters. By identifying transitions between the deep and shallow habitats, we found that most halibut display migrations from the deep waters to shallow waters during the first 3 years of life. After reaching maturity, most halibut distributing in northern regions of the GSL became full-time residents in deep areas of the GSL. In contrast, halibut found in summer on the shallow plateau of the southern GSL displayed migrating behaviour between shallow (summer) and deep (winter) waters throughout their lives, either on an annual or irregular basis. Overall, our results demonstrate that otolith chemical signatures serve as natural markers of geographically distinct marine environments, facilitating the identification and reconstruction of environmental histories of long-lived marine fishes. [ABSTRACT FROM AUTHOR]

Germanium (Ge) is a critical raw material for emerging high-tech and green industries, resulting in considerable recent interest in understanding its distribution and geochemical behavior in ore deposits. In this contribution, the distribution of Ge and related trace elements in the Fule Pb-Zn(-Ge) deposit, South China, is investigated to reveal the distribution of Ge in the hydrothermal ores and during sulfide weathering, using multiple microanalytical techniques, including scanning electron microscopy, electron probe microanalysis and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). In the Fule MVT deposit, sphalerite (ZnS) is the most significant Ge-carrier relative to other sulfides, though the five recognized textural types of sphalerite display progressive depletion in Ge from the first sphalerite generation to the late one. In the early stage, sphalerite with fine-grained chalcopyrite inclusions has the highest Ge concentrations, probably accounting for a significant proportion of the total Ge. We interpret that high Ge concentrations in the early sphalerite may be attributable to high Cu activity in the mineralizing fluids. During oxidative weathering, Ge was redistributed from its original host, sphalerite, to the weathering product willemite (Zn2SiO4) rather than smithsonite (ZnCO3), with high levels of Ge (up to 448 μg/g) present in the willemite. The formation of abundant willemite largely prevents the dispersion of Ge during weathering. In principle, willemite-hosted Ge should be fully recoverable, and the Zn-silicate ores may, therefore, be a potential target to meet future demand. This study provides new information on how Ge behaves from sulfide- to weathering-stage in MVT systems, which directly impacts Ge mobility and deportment changes and the development of metallurgical strategies for Ge recovery. [ABSTRACT FROM AUTHOR]

Understanding processes that occur during pegmatite crystallization are important for understanding magma evolution and enrichment processes of e.g. strategic and rare metals in pegmatites. Several processes are involved in the formation of pegmatites, and among these the timing of fluid saturation and exsolution is a critical area of investigation. The primary question focuses on if the timing of these processes influences pegmatite crystallization and the concentration of elements. The understanding of the relationship between fluid dynamics and mineralization is essential to develop comprehensive models of pegmatite formation. The unidirectional tourmaline prisms and quartz-tourmaline intergrowths (QTIs), composed of a central tourmaline surrounded by skeletal tourmaline intergrown with quartz are anisotropic textures, linked to disequilibrium crystallization at high degrees of undercooling. This study aims to trace fluid saturation and evolution in the outer zones of internally zoned pegmatites and to provide more accurate temperature constraints for their crystallization, using the Emmons pegmatite (Maine, USA) as a case study. The methodology comprises detailed inclusion petrography, microthermometric analyses, Raman spectroscopy, and LA-ICP-MS analyses. The results indicate that localized fluid saturation occurs early during the magmatic stage of pegmatite crystallization. At this point, the crystallizing mineral assemblages are composed of feldspar, muscovite, quartz, tourmaline, and minor garnet. The exsolved fluid is similar throughout the host tourmalines and is characterized by an H 2 O-NaCl-CO 2 -(N 2 -CH 4) composition. Temperatures, which are obtained from primary fluid inclusion isochores vary between 315 °C and 440 °C and confirm that the pegmatite crystallized at undercooled conditions. A decrease in temperature occurs on a centimeter scale between the central tourmaline and the skeletal tourmaline of the QTIs, which could be caused by a nucleation delay within individual boundary layers that are formed around the central tourmaline of the QTI. The higher concentration of water and other incompatible components, including fluxes, in the boundary layer led to fluid exsolution localized at the crystal-melt interface. The increased concentration of fluxes causes a nucleation delay, increasing the degree of undercooling and consequently leading to the skeletal morphologies seen in the QTIs. Furthermore, studied melt inclusions indicate that a compositionally modified melt was present during tourmaline crystallization, confirming the existence of a boundary layer at centimeter to decimeter scale. [ABSTRACT FROM AUTHOR]

A simple and reliable external calibration strategy of LA-ICP-MS for fresh plant soft tissues was developed. The prepared plant suspension was frozen by the designed cryogenic ablation cell and used as external standard for quantitative elemental imaging analysis of fresh plant tissues. The controllable water content of the prepared external standards provides a similar matrix with fresh soft tissues, and a homogeneous elemental distribution could be ensured due to the fine grinding particle sizes. More interestingly, the presence of water increased the signal intensity produced by the suspension by a factor of 1.6 (Pb) to 66.6 (La) compared to that of the pressed cake. The excellent dispersing property and advantage of long-term use were achieved owing to the employment of 0.1% PAANa as suspending agent. A series of plant reference materials were analyzed, and the relative errors of most elements were less than 10 %, indicating that there is a reliable accuracy of the proposed method. The limits of detection (LODs) ranged from 0.1 ng·g−1 (La) to 1279 ng·g−1 (S). This method was used for elemental imaging analysis in rice leaves under arsenic stress, and the results were consistent with previous studies, which mean that the proposed method could provide technical support for researchers in the fields of agriculture and environment. [ABSTRACT FROM AUTHOR]

U–Pb dating of zircon via laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) has become a primary method for determining the age of crystalline rocks and the provenance and maximum depositional age of (meta)sedimentary rocks. Although chemical abrasion has become a standard approach for mitigating Pb loss in zircon dated via high‐resolution thermal ionization mass spectrometry (CA‐TIMS), laser ablation dating is rarely accompanied by chemical abrasion. We evaluate the accuracy of U–Pb dates acquired via LA‐ICP‐MS relative to CA‐TIMS through analysis of a large database of paired analyses from the same zircon crystals. We show that laser ablation 206Pb/238U dates are systematically younger than their CA‐TIMS counterparts, with a greater shift in detrital zircon (−2.0%) versus igneous or metamorphic zircon (−0.9%). Although systematic biases related to “matrix effects” may be a contributing factor, our analysis suggests that unmitigated cryptic Pb loss is likely widespread in laser ablation U–Pb datasets. [ABSTRACT FROM AUTHOR]

The Songshugang deposit is a large Ta–Nb deposit in South China, with Ta–Nb mineralization associated genetically with the granite and pegmatite. A diversity of quartz from topaz–albite granite, quartz–mica pegmatite, quartz–feldspar pegmatite, and quartz–fluorite pegmatite at Songshugang was studied by CL and LA–ICP–MS in order to constrain enrichment mechanisms of Nb and Ta and to find geochemical indicators of quartz for rare metal deposits. Cathodoluminescence image illuminates a canvas of complexity, the quartz from topaz–albite granite, quartz–mica pegmatite, quartz–feldspar pegmatite, and quartz–fluorite pegmatite, exhibits numerous dark CL streaks, patches, and a series of healed fractures. These textures suggest that the rocks were fractured because of deep crustal pressure, and underwent later hydrothermal metasomatism and quartz filling. The quartz from quartz–fluorite pegmatite present limited patches or fractures but distinct growth bands, indicating that the melt fluid composition during the formation of quartz at this stage varies greatly and is less affected by mechanical fragmentation. The LA–ICP–MS analysis of quartz shows that there is a positive correlation between Al and Li in the quartz from topaz–albite granite, quartz–mica pegmatite, quartz–feldspar pegmatite, to quartz–fluorite pegmatite, indicating that Al mainly enters the quartz lattice through charge compensation substitution mechanism with Li. However, our data deviate from the theoretical Li:Al mass ratio of ~ 1:3.89 in quartz, indicating that there may be competition between H+ and Li in a water-rich magmatic environment. The quartz from topaz–albite granite is enriched in K and Na elements, and the quartz from quartz–fluorite pegmatite is enriched in fluorite with a low Ca content in quartz, further elucidating that these rocks were subjected to hydrothermal metasomatism. From topaz–albitite granite to quartz–fluorite pegmatite, Al, Li and Ge content and Al/Ti, Ge/Ti, Sb/Ti ratios in quartz gradually increased, but Ti content gradually decreased, reflecting the high evolution of magma, which can enrich rare metal elements. Based on the characteristics of quartz CL textures and trace elements in topaz–albite granite, quartz–mica pegmatite, quartz–feldspar pegmatite, and quartz–fluorite pegmatite, combined with the albitization and K-feldspathization of rocks, it is suggested that the Nb–Ta mineralization in Songshugang may be influenced by the combined action of magmatic crystallization differentiation and fluid metasomatism. By comparing the quartz in the Songshugang pluton with the quartz in the granite type and pegmatite type rare metal deposits recognized in the world, the Songshugang pegmatite share similarities with the LCT-type pegmatite. Combined with previous studies, the Ge/Ti > 0.1 and Ti < 10 ppm, as well as Al, Li, Ge, Sb, K, Na contents and Al/Ti, Sb/Ti ratios in quartz have the potential to be a powerful exploration marker for identifying granite-like pegmatitic Nb–Ta deposits in other places. [ABSTRACT FROM AUTHOR]

Ultrahigh‐temperature (UHT; >900°C) metamorphism drives crustal differentiation and is widely recognized in the rock record, but its geodynamic causes are debated. Previous work on granulite‐facies metapelite xenoliths from San Luis Potosí, Mexico suggests the lower crust experienced a protracted UHT metamorphic event that coincided with the onset of regional extension. To determine the duration, conditions, and heat sources of UHT metamorphism recorded by these xenoliths, this study characterizes the major‐element, trace‐element, and U‐Pb isotopic systematics of quartz, rutile, feldspar, garnet, and zircon by in situ electron microprobe (EPMA) and laser‐ablation inductively coupled‐plasma mass spectrometry (LA‐ICP‐MS), and augments these data with detailed petrography, thermobarometry, phase equilibria modeling, and diffusion modeling. Thermobarometry and phase equilibria modeling suggest peak metamorphic conditions exceeded 0.7 GPa and 900°C. Zircon petrochronology confirms >15 Myr of UHT conditions since its onset at ∼30 Ma. A small population of zircon record elevated temperatures following transition from backarc compression to extension during the waning stages of orogenesis (60–37 Ma). Garnet preserves trace‐element zoning and mineral inclusions consistent with suprasolidus garnet growth and subsequent compositional modification by intracrystalline rare‐earth element diffusion during protracted heating, with diffusion chronometry timescales in agreement with zircon data, followed by fluid‐driven remobilization of trace elements along now‐healed fractures within ∼1 Myr of eruption. In sum, these data are most compatible with lithospheric mantle attenuation or removal as the dominant heat transport mechanism driving synextensional UHT metamorphism and crustal melting, which has bearing on models for crustal differentiation and formation of modern and ancient granulite terranes globally. Plain Language Summary: The production of melt in the deep crust has important implications for how continents are physically and chemically modified, which in turn controls the distribution of critical mineral resources and the expression of plate tectonics at Earth's surface. One setting where significant partial melting can occur is in a high‐temperature granulite terrane, such as the lower crust beneath the Basin and Range province of southwestern North America. The Basin and Range province is a region where the continent is actively experiencing tectonic extension and, in several places, has been interpreted to have lower crust that was (or is currently) heated to above 900°C. To understand the causality between continental extension in North America and these extreme metamorphic conditions, we study exotic rock fragments of the deep crust beneath San Luis Potosí, Mexico that were brought up by a geologically recent volcanic eruption. These rocks record chemical information that tracks the temperature of the geologically modern lower crust prior to eruption and the duration of extreme temperatures and melting in this crust over the last 60 million years. Using this chemical information, we further our understanding of how tectonic extension is actively driving deep crustal melting beneath southwestern North America. Key Points: Lower crustal metapelite xenoliths from San Luis Potosi, Mexico record ultrahigh (>900°C) temperature (UHT) metamorphismZircon petrochronology suggests protracted (>15 Myr) UHT conditions since the onset of regional extensionGarnet preserves complex trace‐element zoning despite extreme temperatures; garnet diffusion chronometry timescales agree with zircon data [ABSTRACT FROM AUTHOR]

Bark paintings represent a unique artform that originated in Australia and continues to this day. This paper presents a scientific investigation into both the pigments and binders used by Aboriginal artists from across the Northern Territory (NT) and the Kimberley region in Western Australia (WA) and represents the first major study dedicated to identifying these materials in samples taken from paintings. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), Fourier transform infrared (FTIR) and Raman spectroscopy were used to identify the pigments in the four colors commonly associated with works by Aboriginal artists: red, yellow, black, and white. Iron oxides are used for red and yellow. Typically, kaolin is used for white and carbon or natural manganese ores are used for black, although the use of other pigments such as huntite (white) and battery black were seen in paintings from specific locations. Evidence of trade could not be established during this study; however, analysis shows that artists may use different pigments based on location and availability. A combination of FTIR and pyrolysis-gas chromatography-mass spectrometry (pyrolysis-GC-MS) was utilized to investigate the presence of a binder in the paint. Plant-based materials were identified as the binder in the majority of the paintings. The use of orchid juice was common, both as a preparatory layer on the bark substrate and as a paint binder. The presence of synthetic resins was more widespread than anticipated, attributed to both conservation efforts and more modern painting practices. [ABSTRACT FROM AUTHOR]

Forty-six glass finds, including vessel fragments, windows, one inlay and one indicator of production (moil) excavated in the dump of the Sarno Baths in Pompeii were selected for an interdisciplinary technological, typological and chemical study. The identification of the moil demonstrates that a glassblowing workshop most likely existed in Pompeii, thus putting an end to a long-standing scientific debate. The LA-ICP-MS chemical data show that Roman-Mn base glass predominates, along with few Egyptian natron-type glasses and some plant-ash glass of probable Egyptian origin as well. A large proportion of the analysed glass, including the moil, consists of recycled compositions, suggesting the existence of an efficient system of collection and recycling of glass, which was active even at a time when the city had an abundant supply of fresh glass. The demand for raw glass in Pompeii far exceeded the average demand of other Roman towns, because glass containers were essential for the flourishing perfume industry in Pompeii and Campania. The proximity of the Sarno dump to the perfume district in the south-western part of the city and to the horrea of the Sanctuary of Venus suggests the possible location of the glass workshop in this area. [ABSTRACT FROM AUTHOR]

The Iron Age was a period of change, with many innovations in the glass-making technology. The chemical composition of the set of objects considered in the present study demonstrates the diversity of the raw materials used and the depth of knowledge about the manipulation of glass appearance in the eighth-sixth centuries BCE. The study was carried out using fibre optics reflection spectroscopy and portable X-ray fluorescence spectrometry at the museums’ premises to examine a large number of glass beads and preliminarily group them on the basis of their composition and spectral characteristics. In addition, a smaller set of selected samples was analysed by laser ablation inductively coupled plasma mass spectrometry to provide a comprehensive chemical characterisation of the material. The compositional data indicated that the samples belonged to the high magnesium and low magnesium glass compositional types. Only one sample was recognised as low magnesium medium potassium glass. Glasses within each group were made from different sands, suggesting different provenances. Some of the samples were suggested to be of local origin, while the others were interpreted as imported glass. Evidence of glass colouring, decolouring and recycling are also discussed. [ABSTRACT FROM AUTHOR]

The Perron deposit, located in the northern part of the Archean Abitibi belt, bears some of the highest gold-grade mineralization for orogenic-vein-type deposits worldwide (High-Grade Zone: HGZ). More than 13 gold-bearing zones with different sulfide assemblages, hydrothermal alterations, and gold grades have been recently outlined, and they range from volcanogenic to orogenic in origin. In addition, seven zones are hosted in a restricted volume of ~1 km3, which is called the Eastern Gold Zone. Pyrite, sphalerite, pyrrhotite, and chalcopyrite—each from a different gold-bearing zone—were analyzed with LA-ICP-MS to decipher their genetic links, mineralizing processes, and temperature of formation. The temperatures calculated with the sphalerite GGIMFis thermometer range from 348 to 398 °C. All gold-bearing zones recorded volcanogenic hydrothermal inputs at different intensities, manifested by pyrrhotite. Pyrite was late-metamorphic and related to the orogenic gold system induced by the contact metamorphism of amphibolite facies. The pyrrhotite grains had very homogeneous trace element signatures in all zones, which is a characteristic of metamorphic recrystallization, exhibiting a loss of mobile elements (Au, Te, Bi, Tl, Sn, W, In) but high concentrations of Ni, Co, and As. Conversely, the pyrite was systematically enriched with all elements depleted from pyrrhotite, bearing five specific signatures of element enrichments: W, Tl, Sn, In-Cd-Zn, and Bi-Te-Au. For gold-rich zones (e.g., the HGZ), gold was linked to the Bi-Te-Au signature of pyrite, with Bi enrichment occurring at up to 72,000 times the background level in Archean shale pyrite. It was concluded that gold was transported, at least in part, as Bi-Te melts in the previously documented non-aqueous orogenic fluids, hence accounting for the very-high-grade gold content of the HGZ. Genetically, the metamorphism of primary gold-bearing volcanogenic mineralizations was the main source of gold during the overprinting of amphibolite (600 °C) in a metamorphically induced orogenic mineralizing event. A strong volcanogenic pre-enrichment is considered the main factor accounting for the gold endowment of the Eastern Gold Zone. [ABSTRACT FROM AUTHOR]

The Bou Dahar Pb-Zn district, located in the Moroccan High Atlas, is a typical carbonate-hosted Pb-Zn ore district (>30 Mt at 4 wt.% Pb, 4 wt.% Zn). In situ trace element analysis was performed using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) on galena and cerussite from different ore types. The galena is generally enriched in Ag and Sb, secondarily enriched in Cu, with a trace amount of Cd and As, but extremely depleted in Bi and Tl. The main substitution mechanism in galena is (Ag, Cu)+ + Sb3+ ↔ 2Pb2+, and at high Sb concentrations, the further substitution of 2Sb3+ + □ ↔ 3Pb2+ (where □ represents a vacancy) took place. Micro-inclusions of Cu-Sb-bearing minerals (such as tetrahedrite) and Ag-bearing minerals (such as acanthite) may exist in some situations. The features of trace elements in galena show the existence of different coupled substitutions in vein-related ore, breccia-related ore, and strata-bound ore. This suggests that the Bou Dahar district experienced multistage mineralization. The MVT model alone cannot fully explain the ore-forming process. The cerussite replacing strata-bound galena is enriched in Sr, Ba, Ag, and Cu, with minor Sb, As, and Tl. Strontium and Ba are directly substituted with Pb in the cerussite lattice. Copper and Ag are likely present in cerussite as nano-inclusions, which differs from the coupled substitution mechanism of the original galena. High concentrations of Ag may occur due to minor electrum inclusions. The enrichment of Ag, Cu, and Au in cerussite during the oxidation process may guide the optimization of ore processing, especially in extracting valuable trace/minor elements. [ABSTRACT FROM AUTHOR]

Raman spectroscopy and laser ablation‐inductively coupled plasma‐mass spectrometry were used to characterize the chemical composition of 34 red garnet beads from Lower Nubian sites, dated between about 3200 BCE and 600 CE. All beads from the A‐Group to the Meroitic period feature a similar calcium‐poor almandine composition (69%–78% almandine, 15%–22% pyrope, 2%–6% grossular, 3%–9% spessartine), which differs from other calcium‐poor almandine garnet types, sourced mostly from Indian deposits in Antiquity. The Nubian beads constitute a new garnet type, named "cluster I", featuring high yttrium (180 to 1205 ppm), moderately low chromium (13–70 ppm), and high scandium (119–213 ppm) concentrations. Their compositions match with previous and two new analyses from two alluvial garnet deposits, Wadi El‐Haraz and Wadi Abu Dom, near the Fourth Cataract of the Nile in Upper Nubia, about 670 km as the crow flies from the Lower Nubian graves. Garnet trade between the Bayuda desert and Lower Nubia sites, and possibly even Egypt, flourished for almost four millennia. Northeastern Africa is the cradle for the oldest use of a gemstone that is harder than quartz—the red almandine garnet. A Post‐Meroitic bead, the youngest in the assembly, displays an unusual faceting, a diamond tipped drill hole, excellent polish, distinct short‐ and long‐prismatic colorless mineral inclusions, and a calcium‐ and manganese‐poor pyrope composition. This suggests that it was not of a local, Nubian, production, but imported, most probably from a South Asian site. [ABSTRACT FROM AUTHOR]

Banded iron formations (BIFs) archive the relationship between Earth's lithosphere, hydrosphere, and atmosphere through time. However, constraints on the origin of Earth's largest ore deposits, hosted by BIFs, are limited by the absence of direct geochronology. Without this temporal context, genetic models cannot be correlated with tectono-thermal and atmospheric drivers responsible for BIF upgrading through time. Utilizing in situ iron oxide U-Pb geochronology, we provide a direct timeline of events tracing development of all the giant BIF-hosted hematite deposits of the Hamersley Province (Pilbara Craton, Western Australia). Direct dating demonstrates that the major iron ore deposits in the region formed during 1.4 to 1.1 Ga. This is one billion to hundreds of millions of years later than previous age constraints based upon 1) the presence of hematite ore clasts in conglomerate beds deposited before ~1.84 Ga, and 2) phosphate mineral dating, which placed the onset of iron mineralization in the Province at ~2.2 to 2.0 Ga during the great oxidation event. Dating of the hematite clasts verified the occurrence of a ~2.2 to 2.0 Ga event, reflecting widespread, but now largely eroded iron mineralization occurring when the Pilbara and Kaapvaal cratons were proximal. No existing phosphate mineral dates overlap with obtained hematite dates and therefore cannot be related to hematite crystallization and ore formation. New geochronology conclusively links all major preserved hematite deposits to a far younger (1.4 to 1.1 Ga) formation period, correlated with the amalgamation of Australia following breakup of the Columbia supercontinent. [ABSTRACT FROM AUTHOR]

In addition to his astronomical observations the famous Renaissance astronomer Tycho Brahe (1546–1601) was known also for his interest in alchemy. He equipped his castle Uraniborg on the island of Ven with a state-of-the-art alchemical laboratory when it was erected around 1580. After Brahe's death Uraniborg was demolished upon a royal decree from 1601, a process which was completed around 1650. In the present study we have analysed four glass shards and one ceramic shard most likely from the alchemical laboratory and retrieved during an archaeological excavation in 1988–90. Cross sections of the shards have been analysed for 31 trace elements by Laser Ablation Inductively Coupled Plasma with Mass Spectrometry with the aim of detecting any traces of the chemical substances on the inside or outside of the shards used in the laboratory. Four of the elements found in excess on the exterior surfaces of the shards, Cu, Sb, Au, and Hg, are in accordance with the reconstructed recipes of the three Paracelsian medicines for which Brahe was famous—Medicamenta tria. This is the first experimental data casting light on the alchemical experiments that took place at Uraniborg 1580–1599. [ABSTRACT FROM AUTHOR]

The Jinchanghe Pb-Zn polymetallic deposit is a representative distal skarn deposit in the Baoshan block. Due to limited research on the sources of ore-forming metals and trace elemental geochemistry of sulfides, the sources and mineralization environments of the Jinchanghe skarn Pb-Zn polymetallic deposit are still controversial. In this study, copper and sulfur isotopes and trace elements of sulfides from the Jinchanghe Pb-Zn polymetallic deposit were analyzed to reveal the sources of ore-forming materials and the ore-forming environments. The trace elemental analysis results show abundant Co, Ni, Mn and Se elements, and less As, Tl and Sb elements dominantly enter pyrite by isomorphic substitution, except for some Zn and Cu that occur as sulfide inclusions in Py1. Abundant Fe and Mn elements could substitute Zn to enter the sphalerite crystal lattice by the isomorphic substitution mechanism of (Fe2+ + Mn2+) ↔ 2Zn2+, and less Ag and Sb elements could enter the sphalerite by the isomorphic substitution mechanism of (Ag+ + Sb3+) ↔ 2Zn2+. The Cu-S isotopic and trace elemental compositions jointly suggest that the Jinchanghe distal skarn Pb-Zn polymetallic deposit formed from magmatic hydrothermal fluids with a sedimentary host-rock contribution, under mesothermal conditions (260 °C on sphalerite). [ABSTRACT FROM AUTHOR]

Apatite fission track (AFT) dating is now routinely performed using LA‐ICP‐MS, and U‐Pb age data are often acquired at the same time, allowing double dating of individual grains. Furthermore, additional geochemical data, such as REE mass fractions are readily acquired during the analysis. It is therefore of practical interest to identify a single material as a quality control on ages and composition. Here we present AFT and U‐Pb data for the McClure Mountain Syenite (MMS) apatite, already widely used as an age reference material by the U‐Pb community. We performed double dating on 238 grains, in thirteen measurement sessions over two years. The AFT data show remarkable reproducibility with an overall central age of 254.1 ± 5.1 Ma. The U‐Pb results agree with the reference age for individual sessions (and for all data together). The results show that that the McClure Mountain apatite is a valid quality control material for double dating, allowing the use of the same material for both methods. We also propose to extend the quality control using MMS to trace element measurements performed in conjunction AFT and U‐Pb dating. [ABSTRACT FROM AUTHOR]

Innate immune systems alter the concentrations of trace elements in host niches in response to invading pathogens during infection. This work reports the interplay between d-block metal ions and their associated biomolecules using hyphenated elemental techniques to spatially quantify both elemental distributions and the abundance of specific transport proteins. Here, lung tissues were collected for analyses from naïve and Streptococcus pneumoniae-infected mice fed on a zinc-restricted or zinc-supplemented diet. Spatiotemporal distributions of manganese (55Mn), iron (56Fe), copper (63Cu), and zinc (66Zn) were determined by quantitative laser ablation–inductively coupled plasma–mass spectrometry. The murine transport proteins ZIP8 and ZIP14, which are associated with zinc transport, were also imaged by incorporation of immunohistochemistry techniques into the analytical workflow. Collectively, this work demonstrates the potential of a single instrumental platform suitable for multiplex analyses of tissues and labelled antibodies to investigate complex elemental interactions at the host-pathogen interface. Further, these methods have the potential for broad application to investigations of biological pathways where concomitant measurement of elements and biomolecules is crucial to understand the basis of disease and aid in development of new therapeutic approaches. [ABSTRACT FROM AUTHOR]

The aim of this work is to evaluate two quantitative methods, based on the external calibration applied in laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis, known as (i) analytical curve and (ii) one-point calibration, using the concept of matrix matching to quantify three potentially toxic elements (PTEs) in wood samples. These can biologically register changes in the abiotic environment and be applied to monitoring climate change or environmental toxicity. In this case, standard sample preparation was evaluated to prepare the standard pellets using Pinus taeda species as a matrix-matching concept. Six pellets of P. taeda, with different Pb, Cd, and Ba concentrations, were prepared to build the analytical curve and one-point calibration strategies. The LA-ICP-MS parameters were optimised for 206Pb, 208Pb, 112Cd, 114Cd, 137Ba, and 138Ba isotope analysis in wood samples. The two calibration strategies provided 74–110% analytical recovery from certified reference materials and similar results to those obtained by ICP-MS through the acid digestion of environmental wood samples from São Paulo City (Brazil). This demonstrated the applicability of the one-point calibration strategy in quantifying PTEs in wood samples, which could be used with environmental analyses. Differences observed between the Ba isotope results obtained via LA-ICP-MS and ICP-MS quantification were related to sampling by LA-ICP-MS and the ICP-MS sample introduction, as well as to laser matrix and transport effects because of the difference between the wood species evaluated. [ABSTRACT FROM AUTHOR]

This study presents the first comprehensive investigation of perovskite from its type locality (Mineral Mines of Southern Urals, Russia), where this mineral was first described by Gustav Rose in 1839. The new data includes results from precise chemical analyses (electron-probe microanalyzer, LA-ICP-MS) and U-Pb ages (SHRIMP-II) of perovskite. Perovskite occurs in silicate-carbonate veins that transect the marginal parts of the Middle Riphaean Kusinsko-Kopanskaya layered intrusion, previously thought to be skarns. The perovskite crystals range from micrometer-scale grains to up to 11 cm in size. Chemical investigations revealed a low content of trace elements (rare earth elements, Y, Nd, U, Th) compared to perovskites from alkaline ultramafic rocks, silica-undersaturated basic rocks, carbonatites, and kimberlites. The determined age of the perovskite, 535 ± 43 Ma, significantly differs from the 1379 ± 8 Ma age of the Kusinsko-Kopanskaya intrusion, challenging the skarn-origin hypothesis for perovskite. Instead, the findings suggest a carbonatite origin for the perovskite mineralization. This timing indicates a previously unknown stage of endogenic activity on the Western Slope of the Southern Urals. [ABSTRACT FROM AUTHOR]

Mafic layered intrusions constitute a natural laboratory to investigate petrogenetic processes using trace element variations in apatite chemistry. Although these intrusions are related to large igneous provinces, there is a wide range of parameters that can affect the chemistry of the primary melt (i.e. composition of the source, pressure, temperature, oxygen fugacity), followed by possible crustal contamination. In this study, we use a comprehensive dataset of analyses of cumulus and intercumulus apatite from a variety of mafic layered intrusions to demonstrate the use of apatite as a powerful petrogenetic indicator. The dataset (determined in this study and compiled from the literature) comprises electron microprobe and LA-ICP-MS analyses, as well as in-situ LA-MC-ICP-MS analyses of Sr isotopes in apatite from well documented layered intrusions (Sept-Iles, Skaergaard, Bushveld, Panzhihua) and the Sudbury Igneous Complex. For the first time, we show that high values of (La/Nd)N, Th, U, Pb, and As in apatite correlate with high (87Sr/86Sr)initial and are related to contamination with continental crust. An elevated (Gd/Yb)N ratio might indicate melting of a mantle source deep enough to retain Yb in garnet. We also confirm that increasingly negative Eu anomaly and decreasing Sr/Y ratio in apatite are indicators of fractional crystallisation of plagioclase, and that high Sr/Y is indicative of early saturation of apatite and/or delayed crystallisation of plagioclase. The reversal to more primitive compositions caused by magma mixing is expressed by higher Sr, V, Mg and Sr/Y ratio, and lower REE + Y, As and Na concentrations in apatite following magma replenishment. Lastly, we show that apatite signature can efficiently distinguish a mafic from a felsic intrusion using its REE and Sr content coupled to its Eu anomaly. It is also possible to further identify the more primitive from the more evolved parts of a mafic layered intrusion, using the Lu, Th, V and volatile (F/Cl) content to distinguish intercumulus from cumulus apatite, respectively. Finally, identifying a mafic magmatic system using detrital apatite in till will prove useful for provenance and mineral exploration studies. [ABSTRACT FROM AUTHOR]

The study provides a detailed investigation into several representatives of La Tène jewellery. Primarily, it deals with non-metallic decorative inlays from the Late La Tène period, particularly with their application on a metal base. Unique artefacts have been selected for the study, all coming from the Czech Republic and Slovakia. A prime representative of the finds is a torc coming from a La Tène burial site in Prague (Czech Republic, Central Europe). In this geographical context, such finds are rather exceptional. The torc examined is remarkable both in terms of its origin and the production technology utilised, namely the application of decorative inlays made of red opaque glass. Available literature classifies this decorative element as an enamel technique. The highly specific type of red soda high-lead glass applied there was examined using LA-ICP-MS. Based on the trace elements detected, it can be established that the glass is most likely related to contemporary Egyptian production. Other items of the artefact set consist of two Münsingen brooches from Moravia and an exceptional brooch from Slovakia. The latter find was found to be decorated with coral (as confirmed by Raman spectroscopy). Besides identifying the materials of the decorations, we were also able to characterize the binder between individual decorative inlays and their metal base. The analysis of the binder has revealed the presence of birch tar (determined by FTIR and GC/MS). The results obtained expand the knowledge about the production technologies applied to the jewellery from the La Tène period. [ABSTRACT FROM AUTHOR]

Simultaneous U–Pb and U–Th dating using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) was performed on the ca. 0.1 Ma Toya tephra and the ca. 0.08 Ma SS14-28 U–Th zircon reference material. In U–Pb dating, both Th/U and Pa/U partitioning between magma and minerals were considered. In U–Th dating, both abundance sensitivity and molecular interferences on 230Th were reevaluated. As a result, the Toya tephra yielded an accurate weighted mean U–Pb age of 0.103 ± 0.029 Ma (2σ) using zircon and monazite. Conversely, the SS14-28 zircon yielded an inaccurate U–Pb age (0.25 ± 0.10 Ma), which was attributed to low 206Pb signal intensity. Both the Toya tephra zircon and the SS14-28 zircon yielded accurate U–Th model ages of 0.108 ± 0.014 Ma and 0.078 ± 0.007 Ma, respectively. The agreement of U–Pb and U–Th ages for Toya indicates that simultaneous U–Pb and U–Th dating is possible and viable. The inappropriate age of SS14-28 U–Pb age and appropriate U–Th model age also indicates it is preferable to apply both U–Pb and U–Th dating simultaneously for young (<0.4 Ma) zircons to check internal consistency. The proposed double dating approach may be especially useful for small grains when it otherwise would be impossible to obtain multiple ages from a single grain. By adopting simultaneous U–Pb and U–Th dating using LA-ICP-MS, zircon crystallization ages as old as 4.5 Ga to as young as 0.1 Ma (or even younger) can be obtained in a quick and cost-effective manner with a reasonable (~5% at 1σ) uncertainty. [ABSTRACT FROM AUTHOR]

This paper presents the results from analysis of thirty 12th to 13th century glass bangles from Czermno, eastern Poland. Study of the primary glass composition was carried out by laser ablation ICP‐MS and electron probe microanalysis. Lead isotope analyses were conducted to determine the origin of the glass's main raw material. Two types of lead glass were distinguished, high‐lead glass and Slavic lead ash glass, both of which were common in Central and Eastern Europe in the early Middle Ages. Isotopic investigations show that the lead flux for the Slavic glass likely came from the Cracow–Upper Silesia region in southern Poland. [ABSTRACT FROM AUTHOR]

Alzheimer's disease (AD) is a prevalent neurodegenerative disorder characterized by cognitive decline and neuropathological hallmarks, including β-amyloid (Aβ) plaques, Tau tangles, synaptic dysfunction and neurodegeneration. Emerging evidence suggests that abnormal iron (Fe) metabolism plays a role in AD pathogenesis, but the precise spatial distribution of the Fe and its transporters, such as ferroportin (FPN), within affected brain regions remains poorly understood. This study investigates the distribution of Fe and FPN in the CA1 region of the human hippocampus in AD patients with a micrometer lateral resolution using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). For this purpose, we visualized and quantified Fe and FPN in three separated CA1 layers: stratum molecular–radial (SMR), stratum pyramidal (SP) and stratum oriens (SO). Additionally, chromogenic immunohistochemistry was used to examine the distribution and colocalization with Tau and Aβ proteins. The results show that Fe accumulation was significantly higher in AD brains, particularly in SMR and SO. However, FPN did not present significantly changes in AD, although it showed a non-uniform distribution across CA1 layers, with elevated levels in SP and SO. Interestingly, minimal overlap was observed between Fe and FPN signals, and none between Fe and areas rich in neurofibrillary tangles (NFTs) or neuritic plaques (NP). In conclusion, the lack of correlation between Fe and FPN signals suggests complex regulatory mechanisms in AD Fe metabolism and deposition. These findings highlight the complexity of Fe dysregulation in AD and its potential role in disease progression. [ABSTRACT FROM AUTHOR]

Phoenician colonisation of the Iberian Peninsula in the 1st millennium BCE introduced many novel and luxurious goods to the local populations of the Western Mediterranean. Among them, black-appearing glass beads are characteristic of indigenous female burials in Southern Portugal during the 6th century BCE. This study presents the results of the first comprehensive archaeometric investigation of black-appearing glass from Vinha das Caliças 4 (Portugal), and of black-appearing glass from the Iberian Peninsula in general. A multi-analytical approach employing Stereomicroscopic observation of manufacture and use traces, VP-SEM-EDS, μ-XRD, and LA-ICP-MS was used to cover a wide range of questions regarding technology and provenance. All analysed samples are natron glass. All samples of black and white beads are characterized by high Zr and low Sr values typically ascribed to the use of Egyptian sands. A comparison of the results of previous studies from the same site clearly demonstrates at least two geochemical provenances for Phoenician-traded glass beads, located in the Levantine region and Egypt, respectively. Furthermore, different colours of glass in individual polychrome beads exhibit similar trace element patterns, which might suggest these beads could have been produced close to glassmaking sites/regions. [ABSTRACT FROM AUTHOR]