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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]

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]

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]

The metaturbidite‐hosted, ∼380 Ma Dufferin gold deposit, Meguma terrane, northeastern Appalachian Orogen (Nova Scotia, Canada) is an orogenic gold deposit with mineralized saddle reef‐type quartz veins hosted by metasandstones and black slates in a tightly folded anticline. Together with native gold inclusions, genetically related hydrothermal carbonaceous material (CM) in veins occurs as pyrobitumen in cavities and along fractures/grain boundaries proximal to vein contacts and wallrock fragments. Integrating several microanalytical methods we document the precipitation of gold via coupled fluid‐fO2 reduction (via interaction with CM) and pH increase. These changes in fluid chemistry destabilized gold bisulfide complexes, leading to efficient Au precipitation from a gold‐undersaturated (0.045 ± 0.024 ppm Au; 1σ; n = 58 fluid inclusions) aqueous‐carbonic fluid (H2O‐NaCl‐CO2 ± N2 ± CH4). The proposed mineralization mechanism is supported by: (a) a complementary decrease in Au and redox‐sensitive semimetals (As, Sb), and increase in wall rock‐derived elements (i.e., Mg, K, Ca, Sr, Fe) concentrations in fluid inclusions with time; (b) a corresponding decrease in the XCO2, consistent with CO2 removal via reduction/respeciation and late carbonate precipitation; and (c) gold embedding in, or on, the surface of CM inside mineralized cavities and fractures. Despite mineralizing fluids transporting low concentrations of Au far from saturation, precipitation of gold was locally evidently high where such fluids interacted with CM, contributing to the overall gold endowment of Meguma deposits. This work re‐emphasizes CM as a potential prerequisite for efficient gold precipitation within the overall genetic model for similar orogenic metasedimentary settings globally where the presence and/or role of CM has been documented. Plain Language Summary: The Dufferin gold deposit in Nova Scotia, Canada, formed ∼380 million years ago within metamorphosed sedimentary rocks called the Meguma Group. The deposit contains gold‐bearing quartz veins sandwiched between layers of tightly folded rocks. This study focused on unraveling the mechanisms behind some of the gold deposition within this deposit, specifically where associated with carbonaceous matter (CM). We found a close association between gold and CM, which represents organic matter preserved in the rocks. CM is abundant within small cavities throughout the quartz veins that also contain appreciable gold occurring as microscopic particles in the CM. By using a variety of analytical techniques, we determined that efficient gold mineralization occurred in response to specific chemical changes to the gold‐carrying fluid, including a decrease in the oxidation potential and a decrease in the acidity of the fluid through interaction with the CM‐rich rocks. Such changes to the fluid caused gold to become insoluble and form particles that were deposited in the rocks and vein material. Importantly, despite the fluid having a low concentration of dissolved gold, it exhibited a remarkable ability to deposit significant quantities of the precious metal, underscoring the important role of CM in facilitating efficient gold precipitation from fluids. Key Points: First fluid gold concentrations (0.045 ± 0.024 μg/g) measured from an economic, Meguma‐type metasediment‐hosted gold depositFluid Au, S, As, W, and B concentrations comparable to Alpine and Variscan metamorphic fluids hosted in uneconomic, Au‐poor vein systemsGold and carbonaceous matter are coeval and co‐distributed in flysch wallrocks and vein laminae [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]

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]

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]

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]

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]

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]

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]

This study investigates the potential of laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) U‐Pb dating for carbonate nodules in the Late Triassic Ischigualasto Formation of northwestern Argentina. We establish a fully characterized paragenetic sequence to guide the analysis of three pedogenic carbonates and compare the U‐Pb ages with published geochronology from volcanic ashes within the sedimentary succession. Our findings demonstrate the importance of interpreting U‐Pb data within a well‐defined paragenetic framework for accurate age interpretation of pedogenic carbonates. We observe variations in U‐Pb isotopic signatures across different generations of carbonate precipitates and identify syn‐pedogenic and early burial calcite cements as most suitable for precise dating. Respectively, these two calcite cements are interpreted as microcodium and crack‐lining calcite cements formed early in the paragenetic sequence during pedogenesis to early burial of the paleosols as they transitioned from the unsaturated vadose to saturated phreatic zone below the water table. The U‐Pb ages obtained from the carbonate nodules agree with the radioisotopic ages of volcanic ashes, supporting the validity of our dating strategy. These results contribute to advancing U‐Pb carbonate geochronology and highlight its increased potential for dating sedimentary records in the terrestrial realm. Future research should focus on replicating similar work on different carbonate nodules within the Ischigualasto Fm and expanding the application of LA‐ICP‐MS U‐Pb dating to other carbonate‐bearing formations, especially in successions with limited absolute ages or where volcanic ashes are sparse or absent. Plain Language Summary: Carbonate minerals that formed in fossil soils can provide valuable insights into past physical, biological, and chemical processes on Earth's surface. Despite their significance in reconstructing ancient climates and environments, determining the age of these fossil soils via uranium‐to‐lead dating has proven challenging. This difficulty arises from factors associated with soil carbonate minerals, including low uranium content, high lead content, complex formation chemistry, multiple formation episodes (generations), and potential for post‐formation chemical alteration. To address these issues, we first identified the order in which carbonate minerals formed within three samples from the Late Triassic Ischigualasto Formation of Argentina. Then, we dated each generation within each sample and compared the results to identify and understand the most optimal sample locations for dating. Analysis of our data shows that carbonate minerals formed due to biological processes near the surface as well as during the burial and submersion of the fossil soils below the water table are the most suitable for dating and approximate the timing of soil formation. Importantly, the ages from these soil carbonate samples align with ages from volcanic ashes found within the Ischigualasto Formation, thus validating our results and the potential to apply our strategy in other locations. Key Points: A well‐defined paragenetic framework is necessary to interpret laser ablation inductively coupled plasma mass spectrometry U‐Pb data for accurate age interpretation of pedogenic carbonatesU‐Pb isotopic signatures vary across generations of carbonate precipitates, with syn‐pedogenic and early burial cements being the most suitable for precise datingSyn‐pedogenic and early burial cements approximate the timing of pedogenesis and transition from the unsaturated vadose to the saturated phreatic zone, respectively [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]

Rutile stands as a classical mineral within U‐Pb geochronology, offering insights into both magmatic and metamorphic events, and contributing to the understanding of provenance of detrital sedimentary rocks. Addressing the paucity of high‐quality Archaean rutile reference materials suitable for microbeam U‐Pb dating, we present a natural rutile (RKV01) sourced from the Kaap Valley pluton, South Africa, positing it as a potential Archaean reference material. Major element determination was executed via electron probe microanalysis, while trace element determination was conducted using laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS). The determination of U‐Pb ages involved the application of isotope dilution‐thermal ionisation mass spectrometry (ID‐TIMS), secondary ion mass spectrometry (SIMS) and LA‐ICP‐MS. The ID‐TIMS mean 207Pb/206Pb age is 3225.61 ± 0.64 Ma (2s, MSWD = 0.83), interpreted as the best estimate for the crystallisation age. The relatively high U mass fraction (~ 83 μg g‐1), extremely low Th mass fraction (~ 0.003 μg g‐1), negligible common Pb and isotopically homogeneous compositions collectively facilitated precise 207Pb/206Pb age determination via microbeam methods. Both LA‐ICP‐MS and SIMS 207Pb/206Pb ages are characterised by reproducibility and were consistent with the ID‐TIMS age within 2s analytical uncertainty. The results underscore the potential of RKV01 rutile as an Archaean reference material for microbeam U‐Pb dating. [ABSTRACT FROM AUTHOR]

Chemical analysis of glass from African archaeological sites has become a standard research tool over the past decades. Despite the multiplication of studies, the continent still exhibits vast unexplored regions. One of these is the surroundings of Lake Chad. This paper discusses the results of LA‐ICP‐MS analysis of recently excavated glass beads from the late medieval Chadian site of Tié. We demonstrate that the composition of those glass beads largely matches assemblages from along the East African coast. This indicates that most of the beads examined entered the region via a hitherto undocumented east–west Sudanic route linking Northeast Africa with Lake Chad. [ABSTRACT FROM AUTHOR]

The Flinton Group is a metasedimentary succession of the Grenville Province in SE Ontario, potentially allowing insight into the tectono‐thermal evolution of continental crust during the Mesoproterozoic. At its Green Bay locality, Flinton Group metapelites of the staurolite zone contain abundant, post‐kinematic garnet porphyroblasts. Whereas the larger garnet crystals are typically impinged, smaller crystals are isolated from each other, occasionally exhibiting elongated shapes with apparently trigonal morphology. Central sections of the garnet population of a representative sample reveal that garnet is composed of different compositional and microstructural domains. In the largest crystals of the population, garnet contains rectangular to rhombic domains, marked by sharp increases in the concentrations of Nb, V, Ti, and Cr. These domains are associated with irregularly shaped patches, characterized by spatially heterogenous enrichments of Ca and LREE, and depletions in the contents of P, Y, MREE, and HREE, accompanied by increased densities of comparatively coarse‐grained quartz inclusions hosting apatite. Microstructural relationships indicate that these domains correspond to portions of garnet that pseudomorphed biotite, with the enrichments of Nb, V, Ti, and Cr outlining the original biotite shapes. The compositional patterns formed by Ca, P, Y, and REE indicate that apatite participated in the grain‐fluid interactions that operated during the metasomatic replacement of biotite by garnet. The statistical analyses of the garnet number and size distributions confirm that garnet initially nucleated on biotite, controlled by the kinetics of attachment and detachment processes at the garnet/biotite interface, resulting in the typical impingement habit. In situ Lu–Hf garnet geochronology applied to garnet that did not pseudomorph biotite, and hence is enriched in HREE, points to a first metamorphic event at c. 1080 ± 31 Ma. Subsequent pseudomorphism of staurolite by white mica in a Al2O3‐ and FeO‐mobile system resulted in the concomitant crystallization of a new garnet generation, forming overgrowths on the first garnet generation and nuclei in the fine‐grained matrix. Garnet that nucleated during this event grew to isolated and elongated crystals with apparently trigonal morphology, aligned in a direction c. perpendicular to the rock matrix foliation. The open‐system behaviour during this event limits the use of whole‐rock‐based geochronological and thermobarometrical applications. However, previously published in situ U–Pb ages of monazite included in the rims of the garnet crystals and in the rock matrix indicate that this event took place at c. 976 ± 4 Ma, likely associated with a period of increased hydrothermal activity late in the metamorphic history of the Grenvillian Orogeny. Diffusion geospeedometry calculations indicate that garnet growth during this hydrothermal event lasted for less than 6 Myr. [ABSTRACT FROM AUTHOR]

We characterise zircon megacrysts from the Kawisigamuwa carbonatite as a new potential reference material for laser ablation‐inductively coupled plasma‐mass spectrometry U‐Pb and Hf isotope measurement. We studied ten 0.5–4 cm long, brown megacrysts that consist of oscillatory zoned (OZ) and nearly featureless cathodoluminescence‐bright recrystallised (RX) zircon domains. The zircons have low to moderate radiation damage (total α‐dose < 0.5 x 1018 events g‐1), tested by the measured FWHM of the ν3 (SiO4) Raman band < 5 cm‐1. An ID‐TIMS weighted mean 206Pb/238U age of 532.39 ± 0.66 Ma (2s uncertainty) was determined for OZ zircon domains of three grains. While hafnium content varies within and between crystals (6630–9960 μg g‐1) the in situ mean 176Hf/177Hf ratios of ten crystals overlap within uncertainty. We recommend a mean 176Hf/177Hf ratio of 0.282003 ± 0.000020 (2s) as preliminary working value for OZ domains. Two OZ megacrysts yield indistinguishable δ18OVSMOW of 12.1 ± 0.4‰ and 12.2 ± 0.4‰ (2s). Elevated Th/U (> 1.5), Zr/Hf (59–75) and low hafnium contents in OZ domains are similar to those of zircons from carbonatites of mantle origin, while high δ18O and low εHfi (‐15.8 to ‐17.1) indicate a crustal contribution. The zircons probably grew from crustal‐derived carbonate melts under high grade metamorphic conditions. [ABSTRACT FROM AUTHOR]

In this work, we prepared three CaWO4 single crystals (CaW‐0, CaW‐1 and CaW‐3) doped with rare earth elements (REEs) at nominal mass fractions of 50, 250 and 5000 μg g‐1 using the Czochralski method. Electron probe microanalysis (EPMA) and laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) were employed to evaluate the within‐ and between‐unit homogeneity of major elements and REEs, respectively. The within‐unit variation (sr) of 0.40–0.84% and between‐unit sr of 0.14–1.48% for major elements were obtained. Within‐ and between‐unit sr of 0.53–5.56% were also found for REEs by LA‐ICP‐MS spot analyses. A comparison of the sr of repeat analyses was compared with the analytical uncertainty (u), i.e., the mean square weighted deviation (MSWD), which is close to or slightly higher than 1, indicating that no obvious chemical heterogeneity was found in these crystals. Reference values for these elements were obtained through various analytical methods across four different laboratories and applications of the reference materials to calibrating REE mass fractions in a natural scheelite were performed. No significant difference of the results was found as t values are less than 2.75 at the 99% confidence interval. The excellent linearity (R2 > 0.98) between the REE mass fractions and both LA‐ICP‐MS signal intensity and wafer absorbance was found, but the crater height and the absolute mass transported into ICP‐MS decreased when REE mass fractions as well as the colour of crystals increased. These results suggest that the reference materials have the potential to calibrate REE mass fractions in natural scheelite. [ABSTRACT FROM AUTHOR]

We present the results of a study to generate reference glasses that reflect an environment analogous to historic nuclear fallout samples of interest for post‐detonation nuclear forensics. The glasses were generated by melting and then quenching SiO2, Al2O3 and CaCO3 powders. Two suites of glasses with three distinct U isotopic ratios were successfully made with enrichments in the 235U isotope (~ natural [0.72%], ~ 53% and 94%), but the bulk elemental data showed heterogeneity (~ 10% RSD) with U mass fractions ranging from 331.47 to 373.63 μg g‐1. Spatially resolved U isotopic measurements were performed using three mass spectrometry techniques (secondary ion mass spectrometry‐single stage accelerator mass spectrometry [SIMS‐SSAMS], large geometry [LG] ‐ SIMS, and laser ablation‐inductively coupled plasma‐mass spectrometry [LA‐ICP‐MS]) across five National Laboratories. The results showed good agreement with the bulk U isotopic data for the low, medium, and high U mass fractions. We conclude that despite elemental heterogeneity, these samples can serve as useful working reference materials for spatially resolved nuclear fallout analyses, as well as for other related spatially resolved analyses. [ABSTRACT FROM AUTHOR]

Excavations at Soba, the capital of Alwa, between 2019 and 2022 yielded more than 30 glass fragments in addition to a glass cosmetic bottle. An analysis of 30 glass samples has identified glass belonging to a number of compositional groups. The majority of fragments were made of plant ash‐soda glass produced in the Middle East (Iran, Iraq) between the 9th and 10th centuries, and in the Eastern Mediterranean (Levant and Egypt) between the mid‐10th and mid‐12th centuries. Seven fragments were made of mineral–soda‐lime glass produced in 9th‐century Egypt and three high‐lead glasses find analogies in the 9th‐ to 11th‐century glass. Archeological evidence, as well as textual sources, leave no doubt about Alwa's intense transcultural connections. This article provides the first insight into the chemistry of glass shards from medieval Nubia, and the results of analysis contribute to evidence for long‐distance contacts of Soba, the capital of one of the medieval kingdoms of Sahelian Africa. [ABSTRACT FROM AUTHOR]

This study examined the impact of two different transport mechanisms and water/cement (w/c) ratios on the ingress depth of damaging ions into hardened cement paste (hcp). In addition, the effect of sample preparation, i.e. drying before and after exposure, is considered within this study. We applied Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA‐ICP‐MS) as an analytical method to determine the ion ingress depth. The results show that post‐drying of the samples (after exposure) significantly affects the ion ingress depth in hcp as determined by LA‐ICP‐MS. Our results confirmed, as previous studies, that ions ingress the hcp faster due to capillary suction than diffusion. This work shows that although LA‐ICP‐MS is not commonly applied in the analysis of construction material, it has a vast potential to examine the profile ingress of damaging ions. [ABSTRACT FROM AUTHOR]

Columbite‐tantalite LA‐ICP‐MS U‐Pb dating is a fast and useful method to determine the age of rare‐metal deposits and fingerprint the provenance of columbite‐tantalite ore concentrates. Accurate LA‐ICP‐MS U‐Pb dating requires matrix‐matched reference materials. We analysed three columbite‐tantalite samples (SN3, HND and RL2) from China using ID‐TIMS and LA‐ICP‐MS to assess their potential as reference materials for in situ U‐Pb dating. Coltan 139 and these three columbite‐tantalite samples with variable compositions yielded internally consistent LA‐ICP‐MS U‐Pb ages when using each other for calibration and the weighted mean 206Pb/238U ages are comparable to respective ID‐TIMS ages. Composition‐dependent U‐Pb fractionation seems to be insignificant under the LA‐ICP‐MS conditions used. Sample SN3 has a low percentage of heterogeneity for 206Pb/238U ages (4%) with low common Pb contributions (f206 < 1%) and shows a good potential in calibrating unknown samples as primary reference material for LA‐ICP‐MS analysis. Samples RL2 and HND have altered sections characterised by high LREE contents, flat LREE patterns and old 206Pb/238U apparent ages, and are not suited as reference materials. The low 207Pb/206Pb intercepts for samples RL2 and HND lack geological meaning but provide strong evidence that the disturbed U‐Pb systematics with anomalous apparent 206Pb/238U ages is a secondary feature. [ABSTRACT FROM AUTHOR]

Four natural chromite samples (LBS13‐04, LBS13‐06 and LBS13‐13) from the Luobusa ophiolite (China) and 16SW2‐6 from the Stillwater Complex (USA) were developed as reference materials for in situ element microanalysis. Approximately 8 g of chromite fragments with grain sizes of 0.5–1.5 mm from each chromite sample were separated under a binocular microscope and analysed by EPMA, XRF, LA‐ICP‐MS and solution nebulisation ICP‐MS techniques for major and trace elements at six laboratories. The results show that the four chromite samples are homogeneous with respect to MgO, Al2O3, Cr2O3, FeO, Sc, Ti, V, Mn, Co, Ni, Zn and Ga. These samples are thus suitable to be used as reference materials for in situ microanalysis. [ABSTRACT FROM AUTHOR]

A new reference material, STDGL3, for the calibration of in situ analyses of sulfide minerals by LA‐ICP‐MS has been developed and characterised. It represents a lithium‐borate‐based glass containing a mixture of Zn‐ and Fe‐sulfide concentrates doped with several chalcophile elements as well as Zr, Gd, Hf and Ta required for assessing common interferences on Ag, Au and Pt. STDGL3 has a wider range of elements and a better homogeneity compared with existing reference materials for LA‐ICP‐MS analysis of sulfides. Compositional variations for most elements are below 3% RSD, below 5% RSD for Ag, Au and Pt, and below 7% RSD for Se, when performing spot analyses with a 50 μm beam size. Its preparation recipe is reproducible allowing for multiple batches to be made. Use of STDGL3 significantly improves accuracy of sulfide mineral analysis by LA‐ICP‐MS when compared with use of other available reference materials. Performance of STDGL3 was evaluated using several different laser systems. No significant change was observed between 193 nm ArF excimer lasers with 5 and 20 ns pulse widths, but use of 213 and 248 nm lasers displays more systematic differences, especially when analysing galena. Correction coefficients are needed for some elements (Zn and Cd in particular) when analysing sulfide minerals using STDGL3 as a calibration reference material. [ABSTRACT FROM AUTHOR]

Dengjiashan is a large‐scale Pb–Zn deposit discovered in the western part of the Xicheng ore field within the West Qinling metallogenic belt. Information regarding the distribution and occurrence of trace elements in ore minerals and mineralization, as well as the genesis of this deposit, remains scarce. Laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) analysis and elemental mapping were used to determine the distribution and occurrence of trace elements in the sulfide minerals of the Dengjiashan deposit, as well as delineate the process of its genesis. Our results showed that the trace elements enriched in the different sulfides were significantly different. Sphalerite is the main carrier mineral of the scattered elements Cd, Ge and Ga. Based on the trace element content and ratio, principal component analysis and colour of the sphalerite and pyrite, the deposit likely formed in a medium‐temperature environment. The comparative analysis of trace elements from multiple deposits of different origins, combined with the geological characteristics and distribution of sulfide trace elements, suggests that Dengjiashan is a sedimentary exhalative (SEDEX)‐type deposit. As the metallogenic process had a closer relationship to medium‐low temperature hot brine and later tectonic metamorphic hydrothermal fluid, than with magmatic hydrothermal fluid, the deposit is likely of non‐magmatic SEDEX–hot brine superimposed transition origin. This study provides additional insight on the distribution of trace elements in the sulfide minerals of the Dengjiashan deposit, as well as the processes that led to its formation, and may further facilitate ongoing and future key metal prospecting and exploration efforts. [ABSTRACT FROM AUTHOR]

The in situ (U‐Th‐Sm)/He and U/Pb laser‐ablation double‐dating procedure is a valuable method that can provide a large dataset relatively efficiently in contrast with conventional bulk helium thermochronometry. In this study, we evaluate the potential age error associated with the double ablation procedure and report the in situ (U‐Th‐Sm)/He double‐ablation dating of 249 zircons from the Fish Canyon Tuff locality. With LA‐ICP‐MS pseudo‐depth profiling and 3D numerical modelling, we show that the concentric double‐ablation procedure in minerals with U‐Th‐Sm zoning can generate a significant (U‐Th‐Sm)/He age error (positive or negative), resulting in over‐scattering and/or an offset of the mean age. Pseudo‐depth profiling is insufficient to predict the individual age error, partly because of the superimposed ablations. To evaluate the consequence of this inherent bias, we confront a synthetic age distribution to the error expected for U‐Th‐Sm zoned zircons analysed with double‐ablation (U‐Th‐Sm)/He thermochronometry. As expected, a strong age bias causes the spreading of peak ages, downgrading the original signal. Yet, the throughput of the ablation‐based method can allow intra‐ and inter‐sample peak age identification and comparison, and the coupling of (U‐Th‐Sm)/He and U/Pb ages extends our ability to deconvolute a multimodal age spectrum. [ABSTRACT FROM AUTHOR]

Gem quality andradite‐rich garnet (IUC‐1), obtained from the Miocene trachyte dome near Ankara city (Turkey), has been identified as a potential natural secondary reference material for U‐Pb dating. In this study, U‐Pb dating was performed in five different laboratories using isotope dilution TIMS and laser ablation ICP‐MS to determine the homogeneity of euhedral garnet crystals. The U‐Pb ID‐TIMS data for IUC‐1 yielded 207Pb/235U and 206Pb/238U ages of 20.9 ± 0.4 and 20.6 ± 0.8 Ma respectively, and these values are consistent with U‐Pb LA‐ICP‐MS analyses, in which different garnet crystals yielded ages of 20.8 ± 0.1, 20.7 ± 0.1, 20.7 ± 0.2 and 20.2 ± 0.1 Ma. An andradite (IUC‐2) from the Serçeören wollastonite skarn (Turkey) can be used as a secondary reference material provided detailed imaging of the crystals is undertaken. ID‐TIMS data yielded 207Pb/235U and 206Pb/238U ages of 20.4 ± 0.4 and 20.9 ± 1.0 Ma respectively, and yielded U‐Pb ages on different grains of 20.5 ± 0.1, 20.7 ± 1.0, 20.8 ± 1.7 and 20.9 ± 1.6 Ma. The assigned weighted mean age of IUC‐1 (20.4 ± 0.5 Ma, 2s) is proposed as a 2023 reference value. IUC‐1 garnet is expected to contribute significantly to rapidly developing garnet geochronology in the near future. [ABSTRACT FROM AUTHOR]

The last decade has seen a marked increase in U‐Th‐Pb petrochronological studies focused on titanite and apatite. This has motivated the need for detailed, phase‐specific method development and well‐characterised reference materials with a wide variety of ages and chemical compositions. This study presents new U‐Th‐Pb isotope and major‐, minor‐ and trace‐element mass fraction data for ten titanite and five apatite reference materials based on integrated EPMA, LA‐ICP‐MS and isotope‐dilution (ID) multi‐collector (MC)‐ICP‐MS characterisation. Cross‐comparison of EPMA and LA‐ICP‐MS data for the same titanite reference material suite demonstrates that careful selection of EPMA primary reference materials is necessary to minimise inaccuracies. We further identify a significant X‐ray interference when measuring low Ce abundances in Ti‐bearing phases and outline a method for its correction. New ID‐MC‐ICP‐MS and LA‐ICP‐MS data suggest tri‐concordance (defined as concordant ages for the 238U‐206Pb, 235U‐207Pb and 232Th‐208Pb decay systems) of the MKED‐1 titanite reference material and demonstrate the reproducibility of 208Pb/232Th measurements in some secondary titanite reference materials. Integration of 208Pb/232Th results with U‐Pb geochronology provides a meaningful tool to help interpret complex U‐Th‐Pb isotopic age spectra. We provide example applications of 208Pb/232Th LA‐ICP‐MS measurements toward interpreting Archaean titanite ages from the Acasta Gneiss Complex, Northwest Territories, Canada. [ABSTRACT FROM AUTHOR]

U‐Pb dating of andradite‐grossular garnet (grandite) and rutile by LA‐ICP‐MS can be used to constrain various metamorphic, metasomatic and igneous geological processes. In this study, we examine and compare the impact of different analytical conditions (fluence, pulse width, laser beam size and ablation frequency) on the ablation crater morphology, ablation rates, down‐hole fractionation and U‐Pb ages of grandite and rutile samples of different compositions. The shapes of grandite ablation craters suggest the mineral ablates by classical evaporation with significant melting that cannot be eliminated even at fluences just above the ablation threshold. Grandite garnets with higher andradite proportions have faster ablation rates. The overall low U contents of grandite require using large laser beam sizes to obtain acceptable precision of U‐Pb ages. At such conditions and crater depths < 10 μm, fluences of 2.1 and 3.5 J cm‐2, laser pulse width of 5 ns and 20 ns, and ablation frequencies between 3.5 and 6.5 Hz, obtain similar and reproducible ages when the proportion of grossular is < 35%. Rutile ablation crater morphology shows evidence of melt splashing and thermal stress cracking. They have significant crater bottom features, which increase in relief with lower fluences and a higher number of laser shots, indicating the features are probably energy‐related and making higher fluences, such as 5 J cm‐2, necessary for uniform ablation when using 193 nm excimer lasers. The slow ablation rate at low fluences and then steep increase at around 2.0 J cm‐2 suggests a transition in the ablation mechanism from exfoliation to classical vaporisation. Crater bottom features and other ablation behaviour vary between samples, which could be related to their difference in colour. Although the down‐hole fractionation patterns of the samples are similar at 5 J cm‐2, the U‐Pb ages of some samples vary significantly with different analytical conditions and/or measurement sessions, particularly when using laser beam sizes of 30 μm, suggesting differences in mass bias and more variable ablation behaviour. A laser beam size of at least 60 μm is recommended for reproducible U‐Pb dating of rutile. [ABSTRACT FROM AUTHOR]

Although in situ analysis by LA‐ICP‐MS is considered a rapid technique with minimal sample preparation and data reduction, mapping areas of millimetres in size using a small beam (< 15 μm) can be time consuming (several hours) when a quadrupole ICP‐MS is used. In addition, fully quantitative imaging using internal standardisation by LA‐ICP‐MS is challenging in samples with more than one mineral phase present due to varying ablation rates. A new protocol for the quantification of multiple coexisting phases, mapped at a rate of about 12 mm2 h‐1 and a resolution of 12 μm × 12 μm per pixel, is presented. The protocol allows mapping of most atomic masses, ranging from 23Na to 238U, using a time‐of‐flight mass spectrometer (ICP‐ToF‐MS, TOFWERK) connected to a 193 nm excimer laser. A fast‐funnel device was successfully used to increase the aerosol transport speed, reducing the time usually required for mapping by a factor of about ten compared with a quadrupole ICP‐MS. The lower limits of detection for mid and heavy masses are in the range 0.1–10 μg g‐1, allowing determination of trace to ultra‐trace elements. The presented protocol is intended to be a routine analytical tool that can provide greater access to the spatial distribution of major and trace elements in geological materials. [ABSTRACT FROM AUTHOR]

Revealing hydrothermal evolution from the early oxide to late carbonate stages for quartz–wolframite vein‐type deposits is essential for understanding the ore‐forming process. In this study, we choose the Baishitouwa tungsten polymetallic deposit located in the southern Great Xing'an Range tungsten belt as a case study, and present detailed deposit geology and in situ fluid inclusion (FI) analyses including microthermometry, laser Raman spectra, and LA‐ICP‐MS microanalysis to address this issue. Four stages of hydrothermal activity were identified: (1) quartz–wolframite (I), (2) quartz–wolframite (II)–pyrite–chalcopyrite, (3) quartz–polymetallic sulphides, and (4) quartz–carbonate. Four types of FIs were recognized: CO2‐rich, CO2‐bearing, liquid‐rich, and brine inclusions. Microthermometric data showed that the homogenization temperatures and salinities from the early to late stages are 380–460°C, 7.4–17.3, and 29.3–43.2 wt% NaCl equiv., 300–390°C and 7.1–17.0 wt% NaCl equiv., 220–320°C and 2.7–8.1 wt% NaCl equiv., and 150–250°C and 0.5–4.8 wt% NaCl equiv., respectively, suggesting a decreasing trend. Geochemically, all stage fluids contained high Rb and Mn concentrations, high Rb/Na, Cs/Na, Li/Na, K/Na, Rb/Sr, low K/Rb, and consistent Cs/Rb and Cs/(Na + K) ratios, indicating that the mineralizing fluids originated from a common source—an underlying, geochemically uniform, and highly fractionated granitic magma. Fluid immiscibility and cooling are the main mechanisms for wolframite precipitation, whereas greisenization is subordinate; the incursion of meteoric water into the hydrothermal system initiated at the sulphide stage, and fluid mixing is the dominant mechanism for sulphide precipitation. [ABSTRACT FROM AUTHOR]

Christian Nubia was a region with intensive transcultural connections that are visible through the understudied overseas glass bead imports found there. This paper presents the results of an analysis of 20 glass beads from Banganarti, a Christian pilgrim site active during the Makuria kingdom (mid‐sixth to 14th centuries CE). Compositional analyses using laser ablation–inductively coupled plasma–mass spectrometry (LA‐ICP‐MS) have identified glass belonging to a number of broad compositional groups. Two beads were made of mineral soda‐lime glass, dated before the mid‐ninth century CE. Numerous beads were made from plant ash‐soda‐lime glass associated with "Mesopotamian" production dated between the eighth and 10th centuries CE. Lead‐soda‐silica glass has parallels in the ninth–10th centuries glass found in Africa and Europe. One plant ash‐soda‐lime bead was of eastern Mediterranean origin dated after the 10th century CE. Results of this study provide new evidence for provenance and chronology of glass beads available in the mediaeval Northeast Africa as well as contribute new data to the research on the pilgrim and/or trade routes of that time. [ABSTRACT FROM AUTHOR]

Variation among individuals within species is a biological precondition for co‐existence. Traditional geochemical analysis based on bulk averages facilitates rapid data gathering but necessarily means the loss of large amounts of potentially crucial information into variability within a given sample. As the sensitivity of geochemical analysis improves, it is now feasible to build sufficiently powerful datasets to investigate paleoclimatic variation at the level of individual specimens. Here, we investigate geochemical and morphological variation among the sensu stricto, sensu lato and sensu lato extreme subspecies of the workhorse extant planktic foraminifera Globigerinoides ruber. Our experimental design distinguishes between subspecies and intraspecific variability as well as the repeatability of laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS). We show that geochemical variability in Mg/Ca ratios is driven by differences in subspecies depth habitat and that ontogenetic trends in Mg/Ca ratios are evident in the final whorl, with the final chamber consistently showing depleted Mg/Ca. These ontogenetic trends are not driven by individual chamber or test size. The Mg/Ca value variance among individuals is ∼100 times higher than the variance among repeated laser spot analyses of single chambers, directing laboratory protocols towards the need to sample ecologically and environmentally homogeneous samples. Our results emphasize that we can use LA‐ICP‐MS to quantify how individual variability aggregates to bulk results, and highlights that, with sufficient sample sizes, it is possible to reveal how intraspecific variability alters geochemical inference. Plain Language Summary: Planktic foraminifera are small marine life forms whose fossil remains are used to reconstruct past climates and ocean conditions. As with all living things, each individual foraminifer varies from one to the next. Understanding this variation among individuals is important for many branches of science. Here, we studied variation within one of the most used species of foraminifera for paleoceanographic reconstructions, Globigerinoides ruber. We show that the observed geochemical variation is organized within biologically meaningful groups and among life stages. We need the bigger sample sizes we use here to pick apart individual variation and its drivers as future reconstructions of past climates need to consider variation among individuals to get a fuller understanding of the co‐evolution of life and the planet. Key Points: Globigerinoides ruber shows large variability in Mg/Ca ratios that is partially explained by the presence of subspeciesWithin‐specimen variation through ontogeny explains more variation in Mg/Ca ratios than differences among subspeciesSubspecies differences in G. ruber geochemistry are driven by depth habitat differences [ABSTRACT FROM AUTHOR]

U‐Pb Saturn is new freeware for U‐Pb LA‐ICP‐MS data reduction. It has been developed to provide easy interaction with and visualisation of LA‐ICP‐MS U‐Pb datasets, and allows fast and reliable data reduction of hundreds of data‐points. Saturn offers dynamic graphic interfaces to quickly view, evaluate, and plot U‐Pb and Pb‐Pb isotope data. It operates online (or offline), giving the freedom to change parameters and reprocess data at any stage of data acquisition. The main interface allows the user to: (1) choose the best statistics for drift correction, (2) include/exclude offset factors and (3) apply (or not) Pbc corrections in different modes. Signal intensities are displayed in a separate graphic interface that allows users to interact with the time‐resolved signal of individual spot analyses. All graphic windows are interactive; any modification to data treatment (e.g., inclusion or exclusion of analyses of reference material, or modification of the time‐resolved signal windows) is instantaneously updated on the data tables. Saturn is particularly attractive for beginners in LA‐ICP‐MS U‐Pb geochronology as it is non‐commercial, easy to install, and very interactive. Coding information and a version of the software can be accessed at http://www.air.ufop.br. [ABSTRACT FROM AUTHOR]

Laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) is used to compare the suitability of four cassiterite (SnO2) materials (SPG, Yankee, AY‐4 and Jian‐1), and three matrix‐mismatched reference materials (NIST SRM 612, NIST SRM 614 and 91500 zircon) for normalisation of U‐Pb and Pb‐Pb isotope ratios in cassiterite. The excess variance of ages determined by LA‐ICP‐MS is estimated to be ±0.33% for 207Pb/206Pb vs. 208Pb/206Pb isochron ages and ± 1.8% and for U‐Pb ages. Incorporation of this excess variance in cassiterite ages is necessary for realistic uncertainties. 207Pb‐206Pb ages are advantageous for dating Precambrian cassiterite such as SPG compared with U‐Pb ages as matrix effect on instrumental mass fractionation of Pb isotopes are generally considered to be minor. We note minor bias in 207Pb/206Pb vs. 208Pb/206Pb isochron ages (~ 0.6%) when using either the NIST SRM 614 or 91500 zircon reference materials and emphasise the requirement for uncertainty propagation of all sources of error and reference materials with comparable U and Pb mass fraction to the cassiterite. The 238U/206Pb isotopic ratios from normalisation to matrix‐mismatched reference materials show varied results, which emphasises the need to use matrix‐matched reference materials for calculating U‐Pb ages. When cross‐calibrated against each other, LA‐ICP‐MS U‐Pb ages of the ca. 1535 Ma SPG, ca. 245 Ma Yankee and ca. 155 Ma Jian‐1 cassiterites are all consistent with their ID‐TIMS values. [ABSTRACT FROM AUTHOR]

Two clinopyroxene megacrysts, DMP‐2 and DMP‐3, were collected from Cenozoic alkali basalts in the Hannuoba region of China. They were characterised for major and trace element compositions for in situ microanalysis. EPMA and LA‐ICP‐MS analyses indicate homogeneity in the element mass fractions in both clinopyroxene samples. Bulk analyses using various techniques (XRF, ICP‐OES and solution ICP‐MS) also reveal good consistency in their major and trace element data. They, thus, can be used as potential reference materials for elemental in situ microanalysis. Accordingly, element mass fractions are recommended for thirty‐two elements. [ABSTRACT FROM AUTHOR]

Four CGSP (Chinese Geological Standard Powders) carbonate matrix element reference materials were prepared by a coprecipitation method. The major and trace elements were dissolved from natural rare earth carbonate raw materials in strong acid and precipitated with ammonium bicarbonate or ammonia to form carbonate matrix phases. The carbonate reference materials were ground and pressed into tablets for microanalysis. The element homogeneity and stability in CGSP reference materials were tested by LA‐ICP‐MS using a calibration strategy without an internal standard element and evaluated mainly following ISO Guide 35: 2017 and JJF 1343‐2012. Although the homogeneity of most of elements in the CGSP series were comparable to the repeatability obtained from homogeneous glasses, some elements (e.g., Mo, Se, Ga, Ge, Cd, Ni, Co, U) were found to have some degree of heterogeneity. All of elements passed the t‐test evaluation in a 32‐month stability examination except for Mo in CGSP‐A, Na, Ge, Mo in CGSP‐B, Ni, Cd, Sn in CGSP‐C, and Al, P, Tb, Ho in CGSP‐D. The certified element mass fraction values and uncertainties were determined with the characterisation of a non‐operationally defined measurand using various bulk analysis methods in eight laboratories. GGSPs will provide a new carbonate calibration reference option for microanalysis. [ABSTRACT FROM AUTHOR]

The Barrovian metamorphism of the Lepontine dome is manifested by isograds that cross‐cut tectonic nappe contacts, which is commonly interpreted as metamorphism that occurred after nappe emplacement. However, the pervasive mineral and stretching lineation in amphibolite facies, associated with top‐to‐foreland shearing, suggests that peak Barrovian conditions are coeval with nappe‐overthrusting. Here, we combine mapping and U‐Pb zircon dating to better constrain the relation between metamorphism and overthrusting. Metamorphic zircon rims show two age populations at 31–33 and 22–24 Ma. The younger population is locally observed in post‐foliation dikes (and associated metasomatism) likely sourced from deep‐migmatites exhuming along the Alpine backstop. The older population occurs regionally and is found in syn‐kinematic migmatites which occur along a crustal‐scale shear zone. Below this shear zone, magmatic and detrital zircon cores suggest that the Cima Lunga unit, previously interpreted as a tectonic mélange with Mesozoic fragments, was a pre‐Variscan metasedimentary sequence intruded by Permian granitic sills, now orthogneisses. This unit was strongly sheared along the top of the Simano nappe during overthrusting of a rock pile here‐termed Maggia‐Adula nappe. This large‐scale nappe emplacement imprinted the regional lineation and peak temperatures until 31–33 Ma. Péclet (1–10) and Brinkman (0.002–1.8) numbers, estimated for the overthrusting, suggest an advection‐dominated heat transfer caused by rock exhumation, with some diffusion (conduction) during nappe emplacement. Diffusion contributed to Barrovian isograds discordant to the thrust. Shear heating was important if stress times shearing rate >∼5·10−6 W·m−3 within the nappe. The thermal evolution after overthrusting was spatially heterogeneous until ca. 22 Ma. Plain Language Summary: The Lepontine area constitutes the core of the Central European Alps. It has a dome structure and it is internally formed by rock units which register pressure and temperature conditions typical of collisional orogens. The temperatures recorded by minerals are high and the origin of the heat that affected the Lepontine units is still unclear. In this study, we implemented different branches of geology to reveal the age of the Alpine events which juxtaposed the Lepontine units, their provenance and evolution. We performed extensive geological mapping to define the lithologies and structures of rocks. From 13 samples, we extracted 1158 zircon crystals that we analyzed and dated. Fieldwork permitted us to discover new rock units and better characterize the transition between the large‐scale units constituting the Lepontine dome. We propose a geodynamic scenario involving a major large‐scale Alpine unit. The emplacement of this unit generated the main heating event at 31–33 Ma, which is widespread and resulted in peak temperature conditions. The thermal evolution after this event was regionally complex and spatially heterogeneous. Locally in the south we document magmatic/fluid injections at 22–24 Ma, which were sourced from still‐hot regions in the roots of the orogen. Key Points: Geological mapping reveals widespread syn‐tectonic migmatitic rocks along a main crustal‐scale shear zone inside the Lepontine domeAlpine nappe emplacement is regionally recorded at 31–33 Ma, locally overprinted in the south by magmatic/fluid pulses at 22–24 MaMapping and detrital zircon crystals suggest a structurally coherent Cima Lunga unit of pre‐Variscan age, as part of the Simano nappe [ABSTRACT FROM AUTHOR]

Understanding post‐depositional processes altering the layer sequence in ice cores is especially needed to avoid misinterpretation of the oldest and most highly thinned layers. The record of soluble and insoluble impurities represents an important part of the paleoclimate proxies in ice cores but is known to be affected through interaction with the ice matrix, diffusion, and chemical reactions. Laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) has been recognized for its micron‐scale resolution and micro‐destructiveness in ice core impurity analysis. Employing LA‐ICP‐MS for 2D chemical imaging has already revealed a close relationship between the ice grain boundary network and impurity signals with a significant soluble component, such as Na and Mg. Here we show the latest improvements in chemical imaging with LA‐ICP‐MS, by increasing the spatial resolution to 20 μm and extending the simultaneous analysis to also mostly insoluble impurities, such as Al and Fe. All analytes reveal signals of dispersed spots in a sample of an East Greenland ice core. Based on their average size around 50–60 times larger than an average particle and their heterogeneous elemental ratios these spots are interpreted as particle clusters. To distinguish their origin, a simple colocalization classification reveals elemental ratios consistent with marine and mineral dust aerosol. Based on already existing data from cryo‐Raman spectroscopy, we discuss potential ways to integrate the two methods in a future comparison. Such a combined approach may help constraining post‐depositional changes to the dust‐related insoluble impurity components, such as cluster formation and chemical reactions at grain boundaries. Plain Language Summary: Aerosols of marine and terrestrial origin delivered to the polar ice sheets are archived in the ice and can be studied via the analysis of ice cores. The chemical composition and size of mineral dust can deliver important information about past climatic changes and atmospheric transport. However, it has already been shown that this insoluble material is not always passively archived in the ice but can undergo changes in its chemical composition and size, for example, by forming particle aggregates. To investigate these processes, it is preferable to study the chemical composition of insoluble particles and their localization within the ice matrix. Here we show how this can be done by a new chemical imaging method for ice using laser ablation inductively coupled plasma mass spectrometry. In a sample of a Greenland ice core we find clear signals of particle clusters, 50–60 times larger than a single particle. Based on their chemical composition, it is possible to differentiate between marine and terrestrial material. We discuss the results against findings previously obtained for the same sample from a different method, cryo‐Raman spectroscopy. Bringing together several methods may provide important added value for a more comprehensive understanding of these important indicators of past climate. Key Points: Laser ablation inductively coupled plasma mass spectrometry imaging investigates the geochemical composition and localization of particles in samples of the East Greenland Ice Core Project ice core, East GreenlandThe maps reveal clusters of insoluble particles 50–60 times larger than an average particle, at intra‐grain locations and grain boundariesGeochemical signals of the particles are consistent with cryo‐Raman spectroscopy and with known dust sources and sea salt aerosol [ABSTRACT FROM AUTHOR]

In situ238U‐230Th dating was conducted using an ICP‐mass spectrometer coupled with a laser ablation sampling system (LA‐ICP‐MS). To minimise the contribution of mass spectrometric interferences on 230Th, a kinetic energy discrimination technique using a collision/reaction cell (CRC) system was employed. The major problem associated with the CRC‐ICP‐MS system is the lower transmission efficiencies of ions than sector field mass spectrometers. To improve the signal‐to‐background ratio for analytes, a combination of a multiple‐spot laser ablation (msLA) system together with a sensitivity‐enhanced dry plasma cone was employed. Analytical accuracy was evaluated through analyses of three zircon reference materials (GJ‐1, OD‐3 and Plešovice) and the resulting 230Th/238U ratios for GJ‐1 and Plešovice zircons agreed with the secular equilibrium value. The developed technique was applied to Quaternary volcanic zircon and monazite samples from Japan. The resulting ages are 113.5 +5.4‐5.2 ka for the Toya tephra, 105.1 +6.4‐6.1 ka for the Sambe Kisuki tephra, 55.2 +7.7‐7.2 ka for the Hikageyama lava and 16.2 +4.2‐4.1 ka for the Susaki pumice (95% confidence levels). The resulting ages are consistent with previous chronological constraints including zircon fission track ages. The data obtained here demonstrate clearly that the combination of the CRC‐ICP‐MS system and the msLA protocol can become a powerful analytical tool for in situ U‐Th disequilibrium dating. [ABSTRACT FROM AUTHOR]

This new comprehensive in situ mineral‐chemical characterisation of the Happy Jack uraninite has discovered additional information regarding matrix effects and trace element homogeneity, relevant to proposals that it could serve as a reference material (RM). On the LA‐ICP‐MS instrumentation used, there was an absence of discernible matrix effects relative to the silicate glass NIST SRM 610. Lanthanides and Y are found to be very homogeneously distributed in Happy Jack uraninite, Zr, Nb and Ti mass fractions reproducible but only within individual fragments, and other elements still generally heterogeneous. This means that the Happy Jack uraninite can serve as a secondary RM for quality control in studies of natural uraninites. In terms of absolute accuracy and intermediate measurement precision, the Happy Jack uraninite can be used for the homogeneous elements. For elements that are homogeneous within individual fragments only, intermediate measurement precision can still be evaluated, while information values will be obtained for the generally heterogeneous elements. Two distinct groups (high vs. low Zr) were distinguished to exist among different Happy Jack fragments in association with minor variation of REE mass fractions, which possibly explains the observed (heavy) REE discrepancy between in situ laser ablation and bulk solution ICP‐MS analyses. [ABSTRACT FROM AUTHOR]

: Practical methods for determining the ultra‐trace abundances of precious metals in geological materials are needed for research into magmatic and hydrothermal processes and to expand the geochemical footprints of concealed ore deposits. This study presents a new protocol for determining Au, Ag, As, Pt and Re mass fractions in both volcanic glasses and in rock powders prepared as nano‐powder pellets, through the synthesis and refinement of published LA‐ICP‐MS methods. This matrix flexibility allows the method and its limitations to be rigorously assessed for the first time using different volcanic materials. High‐yield laser parameters, interference corrections and low oxide production rates facilitated by laser ablation sampling enabled accurate measurements without chemical pre‐separation. A key finding is that ablation‐remobilised system contamination must be quantified and corrected to make accurate ng g−1‐level Au determinations by LA‐ICP‐MS, resulting in a mean + 2s quantification limit for Au of 0.38 ng g−1. This approach is likely necessary for other ultra‐trace LA‐ICP‐MS analyses of certain elements. Following this correction, the protocol can be usefully applied to both in situ analysis of volcanic materials and efficiently integrated into methods for the determination of major and trace elements in nano‐powder pellets. [ABSTRACT FROM AUTHOR]

Three natural geological glasses (andesitic glass OJY‐1, and rhyolitic obsidians OH‐1 and OA‐1) of specimen sizes 50–150 g were characterised as reference materials for in situ microanalysis of major and trace elements, and Pb isotope ratios. Utilised techniques include isotope‐dilution analyses by TIMS and MC‐ICP‐MS, bulk analyses by XRF, ICP‐OES, ICP‐MS, and microanalysis (10–120 μm spot size) by electron probe microanalyser, LA‐ICP‐MS and LA‐MC‐ICP‐MS. Microanalyses (10–120 μm) indicate that all three glasses are homogeneous with respect to fifty‐four out of fifty‐eight determined elements and Pb isotope ratios, except for Ni in OJY‐1, and Cu, Zr and Ce in OH‐1. The determination of reference values as well as their uncertainties at the 95% confidence level closely followed International Organization for Standardization (ISO) guidelines and the certification protocol of the International Association of Geoanalysts (IAG). These three glasses are fully natural without any subsequent heat treatment, and they represent useful additions to the widely distributed MPI‐DING, USGS and CGSG reference glasses for microanalytical techniques such as electron probe microanalysis, μ‐XRF, LA‐ICP‐MS and SIMS. [ABSTRACT FROM AUTHOR]

The Khan River (Namibia) and Bear Lake (Canada) titanites are investigated as potential reference materials (RM) for LA‐ICP‐MS applications. The Bear Lake titanite is texturally and compositionally homogeneous. The Khan River titanite is texturally heterogeneous and characterised by variable trace element compositions and total rare earth element contents. However, both titanites have consistent U‐Pb and Nd‐isotope ratios. U‐Pb isotope dilution‐thermal ionisation mass spectrometry analyses yielded Pbc‐uncorrected intercept ages of 516.3 ± 1.3 Ma (2s, n = 5, MSWD = 2.4) and 1067.81 ± 0.74 Ma (2s, n = 4, MSWD = 0.35) for Khan River and Bear Lake titanites, respectively. Multiple U‐Pb LA‐SF/MC‐ICP‐MS analyses gave consistent Pbc‐uncorrected intercept ages for both, Khan River (517 ± 1/5 Ma, 2s, n = 262, MSWD = 1.5) and Bear Lake (1070 ± 1/11 Ma, 2s, n = 325, MSWD = 0.88). U‐Pb SHRIMP analyses on the same material returned identical (within uncertainty) ages. Khan River and Bear Lake gave internally consistent solution MC‐ICP‐MS 143Nd/144Nd ratios of 0.511587 ± 0.000027 (2s, n = 2) and 0.512321 ± 0.000004 (2s, n = 2), respectively. The 143Nd/144Nd ratios via solution‐MC‐ICP‐MS and LA‐ICP‐MS all agree within uncertainty and suggest that both titanites can be used as RMs for Nd‐isotope analyses. [ABSTRACT FROM AUTHOR]

Garnet occurs in a wide range of rock types, from mantle peridotites to granites, from eclogites to skarns. In recent years, garnet LA‐ICP‐MS (Laser Ablation Inductively Coupled Plasma Mass Spectrometry) U‐Pb dating has provided a powerful solution for retrieving the ages of rock formations, but successful dating is often prohibited by the low concentration of U. However, the concentration of U, a trace element of garnet, is unknown prior to the LA‐ICP‐MS analysis. In this study, we propose that the U concentration in garnet can be predicted by the contents of major and minor elements, which can be quantitatively obtained by EPMA (electron probe microanalysis). Using a supervised machine learning method (neural network), a model is trained to discriminate U‐rich (>2 ppm) and U‐poor (<2 ppm) garnets, based on EPMA results. Results of cross validation shows that the model has an average accuracy of ∼92% and is a powerful tool in detecting datable U‐rich garnet. To facilitate the use of the discriminator, it is programmed as a stand‐alone Microsoft Excel spreadsheet (HighUGarnet) and users directly paste the molar proportions of garnet end members into it and obtain the discrimination result. [ABSTRACT FROM AUTHOR]

This article examines the production and exchange of kaolin ceramics among Recuay communities in highland Ancash, Peru (ca. 100–700 ce). We draw upon geochemical (laser ablation–inductively coupled plasma–mass spectrometry; LA‐ICP‐MS) and petrographic data to investigate raw material use, provenance, and intraregional trade. We present data on 115 decorated and plain ceramics sampled from nine archaeological sites, which we compare with data on raw kaolin clays. The results indicate a complex network of production and exchange, which included: (1) local production near almost all sites; (2) the limited exchange of ceramic vessels; and (3) the possible distribution of kaolin clay from at least two sources. [ABSTRACT FROM AUTHOR]

Gahnite occurs in diverse rock types and metamorphosed mineral deposits. The gahnite geochemistry is being used as an exploration tool for zinc sulfide deposits. In the present study, the geochemistry of gahnite and associated minerals viz. sphalerite, garnet, sillimanite, staurolite, anthophyllite, biotite, ilmenite, and chlorite, and their petrography have been used in studying the genesis, metamorphic evolution, deposit characterization, and exploration significance of seven Palaeoproterozoic volcanogenic massive sulfides (VMS) deposits in the Betul belt in the Central Indian Tectonic Zone, India. Different textural types of gahnites are recognized in the Betul belt. Field investigations of textural and geochemical characteristics suggest that the gahnites were formed by multiple geological processes: desulfidation of sphalerite, breakdown of almandine garnet, and zincian staurolite, and chloritization of zincian biotite corresponding with regional metamorphism. The temperature conditions of gahnite formation are estimated to be ~600–650°C using empirical Ti in biotite thermometry. The elemental concentrations in gahnites vary from Zn/Fe ratio 2–4; Co 1–30 ppm; Ga 14–573 ppm and Mn 126–3422 ppm, indicating that bimodal volcanics and volcano‐sedimentary rocks as protolith. High Mn content in gahnite suggests an influx of magmatic‐hydrothermal fluid in the protolith. Variations of trace elements (Mg vs. Al/V, Ti vs. Co/Mn, Co vs. V/Ga, Mn vs. Zn/Fe) and high‐temperature of gahnite formation attest to sensu stricto VMS type mineralization in Betul belt, which is entirely different from SEDEX, Broken Hill‐type, and non‐sulfide deposits. Principal component analysis of trace elements shows the geochemical variations at a few deposits and reveals that gahnites were formed as a result of the competing effect of fS2‐fO2 and governed by bulk rock composition. [ABSTRACT FROM AUTHOR]

: Precise age determinations of volcanic deposits from the Late Pleistocene and Holocene are fundamental for hazard assessment. Retrieving accurate radiogenic ages typically relies on analysing specific minerals (such as zircon or sanidine), which are in many cases lacking in the deposits. We present a new 230Th‐238U disequilibrium dating method by LA‐ICP‐MS for inclusion‐bearing ilmenite, and discuss its details and challenges. The technique is tested on ilmenites from the 86.4 ± 1.1 ka Aso‐4 super‐eruption, Japan, and from the Lower Pumice (63.1 ± 4.7 ka) and Upper Pumice (58.4 ± 2.7 ka) eruptions of Nisyros volcano, Greece. Ilmenites of the Aso‐4 eruption produce well‐defined global isochrons yielding ilmenite crystallisation ages of 89 ± 10 ka (2s) and 81 ± 15 ka (2s). Two‐point isochron model ages from the Nisyros eruptions produce youngest population ages of 66.3 ± 5.7 ka (1s) for the Lower Pumice and 61.2 ± 4.4 ka (1s) for the Upper Pumice. The age determinations obtained during this study are compatible with data reported from conventional techniques. These results demonstrate the applicability of this new method to date young volcanic deposits in a quick, reproducible way, and without relying on zircon or K‐bearing phases. [ABSTRACT FROM AUTHOR]

Inter‐session excess variance of U/Pb and Pb/Pb ratios in LA‐ICP‐MS zircon dating is the largest contributor to systematic errors, which in turn limit the accuracy of age determinations. Quantifying long‐term excess variance of reference materials allows for the estimation of excess variance in samples, but such compilations are not available in the literature. Here, we present the results of over 100 measurement sessions over 6 years for seven common zircon reference materials and calculate a characteristic excess variance for each. For 206Pb/238U ages, these values (2s) are as follows: AusZ7‐1 = 1.7% (115 sessions), AusZ7‐5 = 0% (74), OD‐3 = 0.6% (19), Temora2 = 1.2% (86), Plešovice = 1.1% (100), 91500 = 1.0% (146) and Mud Tank = 3.0% (12). For 207Pb/206Pb ages, smaller excess variances are observed: Temora2 = 0.3%, Plešovice = 0.4%, Mud Tank = 1.7% and 91500 = 0.4%. These values are well‐constrained estimates of inter‐session excess variance for the ETH Zürich LA‐ICP‐MS laboratory using a sector‐field ICP‐MS, and may provide either a first‐order estimate for other laboratories or a value to compare against their own reference material compilations. [ABSTRACT FROM AUTHOR]