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Understanding the composition and transport of mineral dust is essential for assessing its environmental and health impacts. We investigated the properties of mineral dust along the urbanized Wasatch Front in northern Utah (USA), comparing it with natural dust collected from upwind locations in the arid Great Basin. Using physical and geochemical analyses, we identified significant differences between urban and natural dust that are not attributable to the intervening landscapes. These differences arise from the mixing of natural dust with local anthropogenic materials, including sediments from the Great Salt Lake playa conditioned by over a century of urban activity. This urban-influenced dust is transported downwind, where it may contribute to elevated levels of cadmium, copper, and zinc in streams of downwind mountain watersheds. These findings underscore the far-reaching impact of urban dust on critical ecosystems and highlight the need for integrated management strategies to mitigate dust-related environmental consequences. 

Glacial meltwater contributions to streams depend on watershed characteristics that impact water quantity and quality, with potential changes as glaciers continue to recede. The purpose of our study was to investigate the influence of glacier and bedrock controls on water chemistry in glacial streams, focusing on a range of small to large watersheds in Alaska. Southcentral Alaska provides an ideal study area due to diverse geologic characteristics and varying amounts of glacial coverage across watersheds. To investigate spatial and temporal variability due to glacial coverage and bedrock type, we analyzed water samples (n= 343) from seven watersheds over 2 years for major and trace element concentrations and water stable isotopes. We found variable water chemistry across the glacial rivers related to glacial coverage and the relative amount of metamorphic, sedimentary, and igneous bedrock. Some sites had elevated concentrations of harmful trace elements like As and U from glacier melt or groundwater. Longitudinal (upstream to downstream) variability was apparent within each river, with increasing inputs from tributaries, and groundwater altering the water chemistry relative to glacier meltwater contributions. The water chemistry and isotopic composition of river samples compared with endmember sources suggested a range from glacier-dominated to groundwater-dominated sites along stream transects. For example, water chemistry in the Knik and Matanuska rivers (with large contributing glaciers) was more influenced by glacier meltwater, while water chemistry in the Little Susitna River (with small glaciers) was more influenced by groundwater. Across all rivers, stream chemistry was controlled by glacier inputs near the headwaters and groundwater inputs downstream, with the water chemistry reflecting bedrock type. Our study provides a greater understanding of geochemical and hydrological processes controlling water resources in rapidly changing glacial watersheds. 

Terminal lakes (without outflow) retain elements and compounds that reach them through fluvial, point source or atmospheric deposition. If the lake sediment is exposed, some of these chemicals could become toxic dust particulates. The Great Salt Lake (GSL) in Utah is a terminal lake that experienced record-low lake elevation in 2021-22, exposing vast areas of playa. Here, we used inductively coupled plasma mass spectrometry to analyze the environmental chemistry of GSL shallow sediment during historic lows in spring, summer, and fall of 2021. Contaminants at the subsurface interface are most able to influence diffusion into the water column and uptake by benthic biota. We focused our analysis on copper, thallium, arsenic, mercury, lead, and zinc, which have been historically deposited in this region and are toxic when at high concentrations. We compared records of regional mining activity to understand the current contamination and assess relevant spatial and temporal gradients. We also used two different extraction methods (EPA 3050b and NH₄AcO at pH=7) that can distinguish “environmentally available” vs. tightly associated and less available fractions. We observed consistent concentration of copper across sites indicating a larger relative impact of atmospheric deposition, with some evidence indicating further impacts of point sources. Arsenic, on the other hand, is maintained at high levels in submerged sediments and is likely geologically- and fluvially- derived. Thallium and mercury fluctuate seasonally and correlate with lake elevation. Lead and zinc levels are relatively low in GSL sites compared with freshwater input sites, indicating the deep brine layer may sequester these heavy metals, preventing their release into the water column. Overall, the concentrations of most metals in GSL sediments have declined from historic highs. However, each contaminant has distinct sources, seasonality, mobility and transmission. Complete recovery (if possible) may require many more decades and individual remediation strategies. 

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. 

Dust events originate from multiple sources in arid and semi-arid regions, making it difficult to quantify source contributions. Dust geochemical/mineralogical composition, if the sources are sufficiently distinct, can be used to quantify the contributions from different sources. To test the viability of using geochemical and mineralogical measurements to separate dust-emitting sites, we used dust samples collected between 2018 and 2020 from ten National Wind Erosion Research Network (NWERN) sites that are representative of western United States (US) dust sources. Dust composition varied seasonally at many of the sites, but within-site variability was smaller than across-site variability, indicating that the geochemical signatures are robust over time. It was not possible to separate all the sites using commonly applied principal component analysis (PCA) and cluster analysis because of overlap in dust geochemistry. However, a linear discriminant analysis (LDA) successfully separated all sites based on their geochemistry, suggesting that LDA may prove useful for separating dust sources that cannot be separated using PCA or other methods. Further, an LDA based on mineralogical data separated most sites using only a limited number of mineral phases that were readily explained by the local geologic setting. Taken together, the geochemical and mineralogical measurements generated distinct signatures of dust emissions across NWERN sites. If expanded to include a broader range of sites across the western US, a library of geochemical and mineralogical data may serve as a basis to track and quantify dust contributions from these sources. 

Abstract Strontium isotope ratios (⁸⁷Sr/⁸⁶Sr) of incrementally grown tissues have been widely used to study movement ecology and migration of animals. However, the time scale of⁸⁷Sr/⁸⁶Sr incorporation from the environment into tissue and how it may influence data interpretation are still poorly understood. Using the relocation of a zoo elephant (Loxodonta africana) named Misha, we characterise and model the⁸⁷Sr/⁸⁶Sr turnover process using high‐resolution measurements of its tusk dentine. We seek to develop a framework that can improve quantitative interpretation of⁸⁷Sr/⁸⁶Sr data in tissues.The⁸⁷Sr/⁸⁶Sr transition associated with the relocation is measured using laser ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) on a prepared tusk slab. We develop a turnover model (BITS), with a rapidly exchanging central pool and a slowly exchanging peripheral pool, in a Bayesian statistical framework. The measured dentine data are first used to calibrate model parameters. The parameters are then used to estimate possible⁸⁷Sr/⁸⁶Sr input time series from two datasets via model inversion: a fidelity test using Misha's dentine data and a case study using published dentine measurements from an Alaskan Woolly Mammoth (Mammuthus primigenius).The LA‐ICP‐MS data are consistent with a two‐compartment turnover process with equivalent half‐lives of 41 days for the central pool and 170 days for the peripheral pool. The model inversion shows good fidelity when estimating the intake⁸⁷Sr/⁸⁶Sr time series associated with Misha's relocation. In the case study, the model suggests an abrupt pattern of change in, and a much wider range of, intake⁸⁷Sr/⁸⁶Sr values than expressed in the woolly mammoth dentine data themselves.Our framework bridges the gap between environmental⁸⁷Sr/⁸⁶Sr variation and data measured in tusk dentine or other incrementally grown tissues. It could be coupled with movement models and additional isotope tracers to study seasonal residency or the spatial and temporal patterns of movement/migration. The generic turnover processes can be adapted to other isotope systems, additional incremental tissues, or other organisms, thus expanding our modelling toolkit to investigate niche partitioning, life history traits and behavioural patterns in conservation biology, archaeology and paleoecology.