Metallicity Research Articles

Exploring the Origin of Cold Gas and Star Formation in a Rare Population of Strongly Bulge-dominated Early-type Galaxies

We analyze the properties of a rare population, the strongly bulge-dominated early-type galaxies (sBDEs) with significant H i gas, using the databases from the FAST All Sky H i survey (FASHI) and the Arecibo Legacy Fast ALFA (ALFALFA) survey. We select the sBDEs from the Sloan Digital Sky Survey and crossmatch with the FASHI-ALFALFA combined H i sample, resulting in 104 H i-rich sBDEs. These sBDEs tend to have extremely high H i reservoirs, which is rare in previous studies such as ATLAS3D. A total of 70% of the selected sBDEs are classified as quiescent galaxies, even though they have a large H i reservoir. We study the properties of these sBDEs from four main aspects: stellar population, gas-phase metallicity, stacked H i spectra, and environment. The majority of H i-rich sBDEs appear to show lower gas-phase metallicity and are located in significantly lower-density environments, suggesting an external origin for their H i gas. We find that star-forming sBDEs exhibit statistically higher star formation efficiency and slightly older stellar populations compared to normal star-forming galaxies, suggesting a recent star formation on the Gyr timescale. They also show narrower and more concentrated H i profiles compared to control star-forming galaxies, which may explain their higher star formation efficiency.

Pyrite trace metal and sulfur isotopic compositions track metalliferous fluid circulation within the Ordovician/Silurian organic-rich black shales in the eastern Sichuan Basin, southwestern China

Depicting metalliferous fluid flows in sedimentary basins has a remarkable implication for understanding the formation and evolution of organic-rich sediments. The Middle-Upper Yangtze region in South China hosts voluminous gaseous hydrocarbons and MVT-type ZnPb deposits. Natural gases are mainly distributed in the Sichuan Basin, yet ZnPb deposits are found in surrounding regions of the basin. Such a unique distribution pattern implies that the interplay between metalliferous fluids and organic-rich sediments may be extensive in the boundary of these two types of deposits. A typical Ordovician/Silurian (Wufeng/Longmaxi formations) organic-rich black shale outcrop occurs in the eastern boundary of the Sichuan Basin. Pyrites are frequently distributed across this section, providing an ideal opportunity to investigate features of metalliferous fluids and their potential impacts on organic-rich sediments. Pyrites associated with high-angle carbonate veinlets are recognized in the studied area, and this group of pyrites (“Group 2”) commonly display planar-laminated morphologies, moderate δ34S values (0.78 ‰–8.86 ‰), and elevated trace metal contents (Ni, Pb, Mn, Mo, Tl, and REE) than those not associated with carbonate veinlets. These features suggest that this group of pyrites may be precipitated via local metalliferous fluid flows. Besides, pyrites with relatively lower trace metal contents can be further divided into two groups, including a group of euhedral/subhedral pyrites with more depleted δ34S values (−18.06 ‰ – -1.15 ‰; “Group 1”) and a group of planar-laminated/cubic pyrites with enriched δ34S values (10.55 ‰–37.62 ‰; “Group 3”). Pyrites of Group 1 and Group 3 may be formed via bacterial sulfate reduction (BSR) and thermochemical sulfate reduction (TSR), respectively. The discovery of fluid-related, trace-metal-enriched pyrites implies that fluid circulation within organic-rich black shales has the potential to remobilize, transport, and re-deposit trace metals. Besides, metalliferous fluid may also promote organic matter maturation within the Sichuan Basin. The outcomes of this study, combined with previous findings of metalliferous fluid flows in the center of the basin and ZnPb mineralization belts surrounding the basin, imply that a widespread Ediacaran-Palaeozoic fluid circulation system may exist in the Middle-Upper Yangtze region.

A seaweed-inspired separator for high performance Zn metal batteries: Boosting kinetics and confining side-reactions

Uncontrolled dendrite growth, sluggish reaction kinetics, and drastic side reactions on the anode-electrolyte interface are the main obstacles that restrict the application prospect of aqueous zinc-ion batteries. Traditional glass fiber (GF) separator with chemical inertness is almost ineffective in restricting these challenges. Herein, inspired by the ionic enrichment behavior of seaweed plants, a facile biomass species, anionic sodium alginate (SA), is purposely decorated on the commercial GF separator to tackle these issues towards Zn anode. Benefiting from the abundant zincophilic functional groups and superior mechanical strength properties, the as-obtained SA@GF separator could act as ion pump to boost the Zn2+ transference number (0.68), reduce the de-solvation energy barrier of hydrated Zn2+, and eliminate the undesired concentration polarization effect, which are verified by experimental tests, theoretical calculations, and finite element simulation, respectively. Based on these efficient modulation mechanisms, the SA@GF separator can synchronously achieve well-aligned Zn deposition and the suppression of parasitic side-reactions. Therefore, the Zn||Zn coin cell integrated with SA@GF separator could yield a prolonged calendar lifespan over 1230 h (1 mA cm−2 and 1 mAh cm−2), exhibiting favorable competitiveness with previously reported separator modification strategies. Impressively, the Zn-MnO2 full and pouch cell assembled with the SA@GF separator also delivered superior cycling stability and rate performance, further verifying its practical application effect. This work provides a new design philosophy to stabilize the Zn anode from the aspect of separator.

Constructing electrochemically stable single crystal Ni-rich cathode material via modification with high valence metal oxides

Single crystal Ni-rich cathode materials (SCNCM) are a good supplement in the market of nickel-based materials due to their safety and excellent electrochemical performance. However, the challenges of cation mixing, phase change during charge/discharge, and low thermal stability remain unresolved in single crystal particles. To address these issues, SCNCM are rationally modified by incorporating transition metal (TM) oxides, and the influence of metal ions with different valence states on the electrochemical properties of SCNCM is methodically explored through experimental results and theoretical calculations. Enhanced structural stability is demonstrated in SCNCM after the modifications, and the degree of improvement in the matrix materials varies depending on the valence state of doped TM ions. The highest structural stability is found in WO3-modified SCNCM, due to the smaller effective ion radii, higher electro-negativity, stronger W–O bond, and efficient suppression of oxygen vacancy generation. As a result, WO3-modified SCNCM have outstanding cycle performance, with a capacity retention rate of 90.2% after 200 cycles. This study provides an insight into the design of advanced SCNCM with enhanced reversibility and cyclability.

Caffeic acid enhances the postharvest quality by maintaining the nutritional features and improving the aroma volatiles for nectarine fruit

Maintaining the quality of postharvest nectarine fruit is considerably challenging owing to their vigorous metabolism processes. This study explored the effectiveness of the natural preservative caffeic acid in extending the shelf-life and improving the flavor quality of nectarine. The decay rate of caffeic acid-treated fruit was only 40.00 % but 73.33 % in control group at the end of storage. Other results showed that caffeic acid inhibited fruit quality deterioration, reflected in weight loss, peel color, pulp softening, respiration rate, malondialdehyde accumulation and ethylene biosynthesis. Findings might be attributed to increased levels of antioxidant compounds, such as ascorbic acid, simple phenols and flavonoids, which maintained high antioxidant capacity and metal reducing power of fruit cells. Notably, the content of phenolics was maintained at 241.11 mg kg−1 in caffeic acid-treated fruit by 8 d, which was only 138.21 mg kg−1 in control. Importantly, nectarine treated with caffeic acid possessed a suitable sugar-to-acid ratio, imparting the fruit with an excellent taste. Additionally, caffeic acid facilitated the effective release of esters and lactones, especially γ- and δ-decalactone with fruity aroma, and prevented green aroma and alcoholic off-flavor. The level of lactones in caffeic acid-treated fruit reached 126.76 μg kg−1 during mid-storage, giving the fruit an attractive flavor quality, while was only 50.61 μg kg−1 in control. Overall, caffeic acid exhibited the potential to preserve the quality of nectarine, ensuring both nutritional and edible value for fruit.

Corrosion behavior of co-gasification slag of furfural residue and coal on alumina-silica refractories

Gasification of furfural residue with coal can realize its efficient and clean utilization. But the high alkali metal content in furfural slag is easy to cause the corrosion of gasifier refractory. Two gasification coals with different silica alumina ratio and a furfural residue were selected in the study. The effects of furfural residue additions on corrosion of silica brick, corundum brick, high alumina brick and mullite brick were investigated by using XRD, SEM-EDS and Factsage Software, and the corrosion mechanism was analyzed. With increasing furfural residue addition, the permeability of the slags to high-aluminium-bearing refractories first decreases and then increases, while the permeability on silica brick shows a slight decrease trend. Leucite (KAlSi2O6) with high-melting temperature is generated from the reaction of K2O and SiO2 in slag with Al2O3 in refractories after furfural residue is added, which hinders the infiltration of slag in refractories. Kaliophilite (KAlSiO4) of low-melting point is formed when K2O content increases, and this contributes to the infiltration of slag in refractories. The acid-base reaction between slag and silica brick is distinctly occurred, more slag reacts with SiO2 in the silicon brick, resulting in a decrease in the amount of slag infiltrating into the silicon brick as furfural residue is added. The corrosion of silica brick is mainly caused by the acid-base reaction, while the corrosion of three alumina based refractory bricks of corundum, mullite and high alumina brick is determined by slag infiltration. A linear correlation between the percolation rate and slag viscosity is established, the slag permeability increases with decreasing viscosity, resulting in stronger permeability for the high Si/Al ratio slag with lower viscosity.

Green synthesis of nano silver-modified date syrup 3D graphene for adsorptive removal of heavy metals from wastewater and its antibacterial efficiency

Abstract Many researchers are focusing on the eco-friendly and cost-effective green synthesis of materials for removing heavy metals from wastewater using materials made from natural sources. In this research, date syrup was used as a rich carbon source while potassium chloride particles were used as a substrate. Green synthesized silver nanoparticles modified the graphene foam to enhance its heavy metal removal and antibacterial efficiency. The morphology and structure of the graphene foam were examined using scanning electron microscopy and Raman spectroscopy. The Brunauer-Emmett-Teller method examines textural features such as surface area, pore volume and diameter. The study focused on evaluating the efficiency of removing heavy metals including cadmium, lead, zinc, and chromium from water. The results indicated that the date syrup graphene foam has high heavy metal removal efficiency despite the short contact time, especially for Cd2+ and Pb2+, with removal efficiencies of 68% and 39%, respectively. It shows a relatively lower efficacy for Zn2+ and Cr2+, with removal efficiencies of 10% and 27%, respectively. The addition of silver nanoparticles greatly improved the removal efficiency of Cd2+ (75%), Zn+2 (22%), and Cr2+ (33%). Moreover, the antibacterial efficacy test showed significant improvement after the nanosilver modification to reach a 100% bacterial-killing rate.

Magnetic Field Geometry of the Gamma-Ray Binary PSR B1259–63 Revealed via X-Ray Polarization

Some X-ray binaries containing an energetic pulsar in orbit around a normal star accelerate particles to high energies in the shock cone formed where the pulsar and stellar winds collide. The magnetic field geometry in the acceleration region in such binaries is unknown. We performed the first measurement of the polarization of the X-ray synchrotron emission from a gamma-ray-emitting binary system. We observed PSR B1259–63 with the Imaging X-ray Polarimetry Explorer during an X-ray bright phase following the periastron passage in 2024 June. X-ray polarization is detected with a polarization degree of 8.3% ± 1.5% at a significance of 5.3σ. The X-ray polarization angle is aligned with the axis of the shock cone at the time of the observation. This indicates that the predominant component of the magnetic field in the acceleration region is oriented perpendicular to the shock-cone axis.

A Census from JWST of Extreme Emission-line Galaxies Spanning the Epoch of Reionization in CEERS

We present a sample of 1165 extreme emission-line galaxies (EELGs) at 4 < z < 9 selected using James Webb Space Telescope (JWST) NIRCam photometry in the Cosmic Evolution Early Release Science (CEERS) program. We use a simple method to photometrically identify EELGs with Hβ + [O iii] (combined) or Hα emission of observed-frame equivalent width (EW) > 5000 Å. JWST/NIRSpec spectroscopic observations of a subset (34) of the photometrically selected EELGs validate our selection method: All spectroscopically observed EELGs confirm our photometric identification of extreme emission, including some cases where the spectral-energy-distribution-derived photometric redshifts are incorrect. We find that the medium-band F410M filter in CEERS is particularly efficient at identifying EELGs, both in terms of including emission lines in the filter and in correctly identifying the continuum between Hβ + [O iii] and Hα in the neighboring broadband filters. We present examples of EELGs that could be incorrectly classified as ultrahigh redshift (z > 12) as a result of extreme Hβ + [O iii] emission blended across the reddest photometric filters. We compare the EELGs to the broader (subextreme) galaxy population in the same redshift range and find that they are consistent with being the bluer, high-EW tail of a broader population of emission-line galaxies. The highest-EW EELGs tend to have more compact emission-line sizes than continuum sizes, suggesting that active galactic nuclei are responsible for at least some of the most extreme EELGs. The photometrically inferred emission-line ratios are consistent with interstellar medium conditions with high ionization and moderately low metallicity, consistent with previous spectroscopic studies.

Grids of stellar models with rotation

Context. Grids of stellar evolution models with rotation using the Geneva stellar evolution code (GENEC) have been published for a wide range of metallicities. Aims. We introduce the last remaining grid of GENEC models, with a metallicity of Z = 10−5. We study the impact of this extremely metal-poor initial composition on various aspects of stellar evolution, and compare it to the results from previous grids at other metallicities. We provide electronic tables that can be used to interpolate between stellar evolution tracks and for population synthesis. Methods. Using the same physics as in the previous papers of this series, we computed a grid of stellar evolution models with GENEC spanning masses between 1.7 and 500 M⊙, with and without rotation, at a metallicity of Z = 10−5. Results. Due to the extremely low metallicity of the models, mass-loss processes are negligible for all except the most massive stars. For most properties (such as evolutionary tracks in the Hertzsprung-Russell diagram, lifetimes, and final fates), the present models fit neatly between those previously computed at surrounding metallicities. However, specific to this metallicity is the very large production of primary nitrogen in moderately rotating stars, which is linked to the interplay between the hydrogen- and helium-burning regions. Conclusions. The stars in the present grid are interesting candidates as sources of nitrogen-enrichment in the early Universe. Indeed, they may have formed very early on from material previously enriched by the massive short-lived Population III stars, and as such constitute a very important piece in the puzzle that is the history of the Universe.

Convert food waste into easily biodegradable liquid substrate: New insights into wet oxidation as a pretreatment for anaerobic digestion

This study is the first comprehensive investigation into the industrial application of wet oxidation (WO) for food waste (FW) valorization. We analyzed the physicochemical properties of WO products and performed a material flow analysis. WO achieved a 25.7 % reduction in chemical oxygen demand and produced liquid and solid products suitable for high-value applications. The liquid product featured high biodegradability (B/C ratio of 0.65), significant BOD5 (33 ± 9 g/L), low total solids (3.5 % ± 0.4 %), and low metal concentrations, making it ideal for high-efficiency anaerobic digestion or as a carbon source in wastewater treatment. The solid product, with a total solids content of 63.9 % ± 1.4 %, is a potential organic fertilizer alternative. Life cycle assessment showed that WO-related scenarios offered superior greenhouse gas (GHG) reduction compared to conventional anaerobic digestion (11.30 kg CO2-eq/t FW slurry). The most effective scenario, combining WO with a carbon source and organic fertilizer alternative, achieved a GHG reduction of −21.80 kg CO2-eq/t FW slurry. Consequently, this study demonstrates that WO, as a pretreatment for food waste valorization, is both technically feasible and environmentally sound, offering valuable engineering references for the implementation of high-efficiency anaerobic digestion processes for food waste.

Synthesis of various types of green biosorbents materials for removals of sulphates from contaminated water for better aquatic environments

Human and industrial activities pollute water resources with sulphur metal, endangering human health and ecosystems. Chemical precipitation and membrane filtration are expensive when treating large amounts of water, inefficient at low metal concentrations, and produce large amounts of toxic sludge and other products that must be disposed of waste water bio-sorption is eco-friendly and alternative. These methods are cheaper, more accessible, and reusable than conventional ones. This study investigates the bio-sorption of sulphur from contaminated water using neem leaf, custard apple leaf, mango tree leaf, orange peels, and banana peels biological waste materials. This work achieves 100 % removal efficiency. Biosorbents remove sulphates from contaminated water: custard leaves 100 % at 4gm, orange peels 40 % at 5gm, tea waste 50 % at 4gm, neem leaves 70 % at 5gm, and mango leaves 75 % at 5gm. The performances of biosorbents for removals of sulphates from water as follows: Custard leaves waste > Mango leaves > Neem leaves > Tea trash > Orange peels the sulphate reduction by biosorbents. The best biosorption occurred at basic pH 6.5, 3.7gm dosage, 90 min contact duration, 30 °C temperature, and 120 rpm agitation speed. The effects of contact time, agitation speed, adsorbent dosage, pH, and temperature are also examined. Before usage, biosorbents materials can be physically and chemically measured the changes. Regenerating and reusing bio-sorbent after sulphates removals makes the method cost-effective for removals of pollutants from water.

The R-process Alliance: Fifth Data Release from the Search for R-process-enhanced Metal-poor Stars in the Galactic Halo with the GTC* * This paper includes data gathered with the 10.4 m Gran Telescopio Canarias located at La Palma, Canary Islands, Spain.

Understanding the abundance pattern of metal-poor stars and the production of heavy elements through various nucleosynthesis processes offers crucial insights into the chemical evolution of the Milky Way, revealing primary sites and major sources of rapid neutron-capture process (r-process) material in the Universe. In this fifth data release from the R-Process Alliance (RPA), we present the detailed chemical abundances of 41 faint (down to V = 15.8) and extremely metal-poor (down to [Fe/H] = −3.3) halo stars selected from the RPA. We obtained high-resolution spectra for these objects with the HORuS spectrograph on the Gran Telescopio Canarias. We measure the abundances of light, α, Fe-peak, and neutron-capture elements. We report the discovery of five carbon-enhanced metal-poor, one limited-r, three r-I, and four r-II stars, and six Mg-poor stars. We also identify one star of a possible globular cluster origin at an extremely low metallicity at [Fe/H] = −3.0. This adds to the growing evidence of a lower-limit metallicity floor for globular cluster abundances. We use the abundances of Fe-peak elements and the α-elements to investigate the contributions from different nucleosynthesis channels in the progenitor supernovae. We find the distribution of [Mg/Eu] as a function of [Fe/H] to have different enrichment levels, indicating different possible pathways and sites of their production. We also reveal differences in the trends of the neutron-capture element abundances of Sr, Ba, and Eu of various r-I and r-II stars from the RPA data releases, which provide constraints on their nucleosynthesis sites and subsequent evolution.

Subsurface Superoxide Spans the Baltic Sea

AbstractSuperoxide is a reactive oxygen species that is influential in the redox chemistry of a wide range of biological processes and environmental cycles. Using a novel in situ sensor we report the first water column profiles of superoxide in the Baltic Sea, at concentrations higher than previously observed in other oceans. Our data revealed consistent peaks of superoxide (2.0–15.1 nM) in dark waters just below the mixed layer. The oxic waters, low metal concentrations, and lack of sunlight imply that the peak is likely of biological origin. Several profiles displayed a concomitant dip in dissolved oxygen mirroring this superoxide peak, strongly suggesting a link between the two features. The magnitude and distribution of superoxide observed warrants re‐evaluation of the most relevant sources and controls of superoxide in seawater. Locally, these high concentrations of superoxide may create environments conducive to reactions with trace metals and organic matter and present an overlooked sink of oxygen in the Baltic Sea.

Synergistic catalytic degradation of Methotrexate using Ce-based high-entropy metal oxides: Insights from DFT calculations and CWPO performance

Methotrexate (MTX), a widely used anticancer drug, is a refractory organic pollutant posing serious threats to ecosystems and human health. This study focuses on the development of a novel catalyst composed of Ce-based high-entropy metal oxides (NHEMO) supported on nepheline for the catalytic wet peroxide oxidation (CWPO) process, targeting MTX degradation in simulated wastewater. The NHEMO catalyst exhibited a unique high-entropy structure that enhances catalytic performance by facilitating diverse electronic interactions, which was confirmed through X-ray diffraction (XRD) and transmission electron microscopy (TEM) analyses showing a well-defined crystal structure and uniform dispersion of metal oxides. Additionally, X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDS) revealed a stable metal composition and high oxidation states of active metal sites. At a reaction temperature of 160 °C, with a residence time of 150 s and an oxidation coefficient of 5, the catalyst achieved a MTX removal rate of 93.49 % and a chemical oxygen demand (COD) removal of 99.95 %. Density Functional Theory (DFT) calculations further demonstrated that H2O2 decomposes into both adsorbed (surface-bound) and free (solution-phase) hydroxyl radicals (·OH). These radicals synergistically degrade MTX through both radical and non-radical pathways, ensuring comprehensive pollutant breakdown. The catalyst also showed excellent stability and a very low metal dissolution rate during the reaction, maintaining high catalytic activity after repeated recycling. This catalyst offers high cost-effectiveness, activity, and stability, providing a promising solution for treating refractory organic pollutants in pharmaceutical wastewater.

First full-scale application of barium carbonate as an effective dispersed alkaline substrate for sulfate removal from acid mine drainage

A full-scale passive treatment plant using barium carbonate (BaCO3), the mineral witherite, as a Dispersed Alkaline Substrate (DAS) for strongly contaminated acid mine drainage was implemented for the first time globally at Mina Concepción, located in the Iberian Pyrite Belt (SW Spain). The plant was monitored over a 105-day period, covering the wettest months of the hydrological year and with a mean flow around 4 L s−1. The AMD treated in the plant exhibits a high strength, with an average sulfate concentration around 1500 mg L−1 and net acidity close to 1000 mg L−1 as CaCO₃ equivalent. According to the above, the loading rate for SO4 and Fe was around 400 and 80 kg day−1, respectively. The treatment process produced an alkaline effluent with low metal content. Nearly complete removal of most metal(loid)s was achieved, with significant sulfate decrease to below 500 mg L−1 in the alkaline outflow of the barium carbonate tank. Barium carbonate demonstrated superior performance compared to magnesia, particularly in enhancing alkalinity and lowering net acidity and concentrations of sulfate and manganese. The high efficiency attained by the plant after the barium carbonate treatment is evidenced by compliance with environmental water quality standards for most contaminants.

Mechanical property, corrosion behavior and cytocompatibility of CoCrMo for dental application: A comparative study of cast and laser powder bed fusion

In this work, by employing powders sourced directly from the original ingot for additive manufacturing, we enabled a comparative overview of the performance between CoCrMo manufactured via laser powder bed fusion (LPBF) and those in their original cast condition. Microstructural analysis revealed that the cast (CT) alloy predominantly consisted of coarse grains with distribution of sigma phase, while the LPBF process resulted in a refined grain structure devoid of the sigma phase. The tensile strength tests demonstrated that the LPBF-derived CoCrMo alloy had substantially greater tensile strength, and ductility compared to CT alloy. Corrosion tests indicated superior corrosion resistance in the LPBF alloy, albeit with a lower metal ion release. In vitro assays confirmed that LPBF CoCrMo alloys displayed favorable cytocompatibility. Consequently, it is concluded that the CoCrMo alloy processed through laser powder bed fusion exhibited enhanced mechanical performance and corrosion resistance. These improvements are primarily attributed to the transformation of the original coarse columnar grain structure through the LPBF technique.

Calibrating and Standardizing the Tip of the Red Giant Branch in the Small Magellanic Cloud Using Small-amplitude Red Giants

We investigate the absolute calibration of the tip of the red giant branch (TRGB) in the Small Magellanic Cloud (SMC) using small amplitude red giant stars (SARGs) classified by the Optical Gravitational Lensing Experiment (OGLE). We show that all stars near the SMC’s TRGB are SARGs. Distinguishing older and younger RGs near the tip according to two period–luminosity sequences labeled A and B, we show many similarities among SARG populations of the Large Magellanic Cloud (LMC) and the SMC, along with notable differences. In particular, SMC SARGs have shorter periods due to lower metallicity and smaller amplitudes due to younger ages than LMC SARGs. We discover two period–color relations near the TRGB that span all A-sequence and B-sequence stars in the OGLE-III footprints of the SMC and LMC, and we investigate using periods instead of color for TRGB standardization. Using variability-derived information only, we trace the SMC’s age and metallicity gradients and show the core to be populated by younger, more metal-rich RGs. The B-sequence yields the brightest and most accurate calibration (M F814W,syn = −4.057 ± 0.019(stat.) ± 0.029(syst.) mag), which we use to measure the distance modulus difference between the Clouds and investigate metallicity effects. Distance measurements not informed by variability should employ the SARG-based calibration based on all stars near the tip (M F814W,syn = −4.024 ± 0.041(stat.) ± 0.029(syst.) mag). Our work highlights the impact of RG population diversity on TRGB distance measurements. Further study is needed to unravel these effects and improve TRGB standardization.

Iron Isotopes reveal volcanogenic input during Oceanic Anoxic Event 2 (OAE 2 ∼ 94 Ma)

Anomalously high metal concentrations including iron enrichments are recorded in marine carbonates deposited during Ocean Anoxic Event 2 (OAE 2). These metal enrichments have been attributed to massive submarine eruptions during the formation of one or more large igneous provinces, the proposed trigger for OAE 2 (hydrothermal hypothesis), or to the release of metals from the reoxidation of formerly anoxic marine sediment during a period of temporary cooling during OAE 2 (sediment release hypothesis). Here we use iron stable isotopes to help distinguish between the two hypotheses for a trace metal enriched interval during OAE 2 in the Iona-1 core in the Western Interior Seaway, Texas. Our results show a two-step negative excursion during OAE 2 that is coincident with osmium isotope volcanic proxies measured in the same core, with peak negative values centered on a trace metal-enriched interval. After corrections for detrital and locally supplied iron to the study setting, the δ56Fe value of the remotely supplied iron is –0.28 ± 0.05 ‰, falling in the range of iron δ56Fe values observed in modern hydrothermal plumes (–0.1 to –0.5 ‰), thus supporting the hydrothermal hypothesis as the source of iron and other associated trace metals enriched in the study core during OAE 2. By contrast, the sediment release hypothesis predicts much lower δ56Fe values, between –1.0 ‰ to –3.3 ‰ predicted for benthic supplies of iron from anoxic marine sediment overlying re-oxygenated bottom waters. This study shows that combining iron with other proxies for environmental change, particularly submarine volcanism, can distinguish hydrothermally supplied iron from dust, rivers, and shelf sediment supplies of iron despite iron’s reputation for complicated cycling.

Flower-like boron-doped zinc single-atom nanozymes for colorimetric sensing and smartphone-assisted detection of Cr(VI)

With the development of electronics, electroplating, printing, and dyeing industries, environmental pollution caused by hexavalent chromium (Cr(VI)) has become increasingly prominent. Skin contact with Cr (VI) can cause allergies or genetic defects, and inhalation can cause cancer, which is a lasting danger to the environment and the human body. Developing effective strategies to monitor Cr(VI) in environmental water or industrial wastewater can evaluate the degree of water pollution and risk warning, thus helping to prevent the spread of Cr(VI) pollution, promote the protection of water resources and the ecological environment, and ensure human safety and sustainable development. On the basis of the regulation of dopamine, boron-doped zinc single-atom nanozymes (Zn/B-NC SAzymes) with three-dimensional nanoflower morphology were controlled in this work. The introduction of B in Zn/B-NC SAzymes and the high metal loading of Zn (6.5 wt%) led to the formation of more active sites, resulting in the material showing excellent enzyme-like activity. H2O2 decomposed to generate superoxide radicals under the catalysis of Zn/B-NC SAzymes, which then oxidized the substrate 3,3′,5,5′-tetramethylbenzidine (TMB) to generate blue oxTMB. When Cr(VI) was introduced into the sensor system, the color of blue oxTMB is deepened, and the colorimetric method of Cr(VI) was constructed. The linear range is 0.2–40 μM, LOD is 59 nM, and the visual detection of Cr (VI) is performed with the aid of the smartphone. This work not only provides experimental and theoretical guidance for understanding the active centers of Zn-SAzymes and their catalytic processes, but also provides a promising and alternative detection strategy for the rapid and even visual on-site detection of Cr(VI) in aquatic environments, which is of great significance for the control of Cr(VI) pollution in the environment and industrial wastewater.