Isotopic Signatures Research Articles

Recent advancements in meat traceability, authenticity verification, and voluntary certification systems

The growing demand for transparency in the food industry has led to significant advancements in meat traceability. Ensuring the authenticity and origin of meat products is critical for consumer trust, public health, and compliance with regulations. This paper reviews recent innovations in meat traceability, with a focus on blockchain technology as a novel approach to ensuring traceability. Additionally, advanced methods for verifying meat authenticity and origin, such as isotope fingerprinting, DNA analysis, and spectroscopic methods, are discussed. The role of voluntary certification schemes in enhancing traceability and authenticity verification in the meat industry is also explored. The findings highlight the importance of integrating cutting-edge technologies and certification schemes to build a robust and transparent meat supply chain.

First direct measurements of the nitrogen isotopic composition of vehicle tailpipe-emitted NH3 and implications for the source apportionment of NH3 in urban atmosphere.

The introduction of three-way catalytic converter (TWC) to meet stringent vehicular NOx emission standards worldwide has led to an unintended consequence of vehicle-derived ammonia (NH3) emission, which might degrade air quality and affect human health, especially in urban areas. The nitrogen stable isotope composition of NH3 (δ15N-NH3) may be a useful tool to trace NH3 sources, but the isotopic signature of vehicle-emitted NH3 is lacking. Here we report the δ15N-NH3 measured from tailpipe exhausts collected directly from 19 different vehicles equipped with TWC using "grab" sample technique optimized to avoid isotopic fractionation. We found a large of range of NH3 concentration (from 1 to 37 ppm, x̄ ± 1σ = 10 ± 8 ppm) and δ15N value (from -38.1 ‰ to 49.0 ‰, x̄ ± 1σ = 1.2 ± 20.9 ‰) for our samples (n = 57). Our results indicate a correlation between δ15N-NH3 and NH3 concentrations (i.e. δ15N-NH3 (‰) = 16.9(± 2.2)In(NH3 concentration; ppm) - 31.7(± 4.7) (R2 = 0.53, P < 0.01) that is associated with the catalyst temperature, which is generally agree with the results of theoretical calculation. After consideration of the vehicle emission evolution, dominant driving condition and tunnel δ15N-NH3 variation, a representative δ15N-NH3 value (meanminmax) of vehicle source is identified as 0.8000-2.20005.2000, which is distinct from (larger than) other NH3 volatilization-related emission sources. Using our newly measured δ15N values and Bayesian mixing model, we approximate the overall contribution of vehicles to ambient NH3 before, during, and after an international event in Beijing was 14.1 %, 7.9 %, and 21.5 %, respectively, which agree well with the course of traffic restriction. Collectively, our findings demonstrate the importance of using vehicle-emitted δ15N-NH3 to quantify vehicular NH3 contribution in urban atmospheres.

Presolar Grains as Probes of Supernova Nucleosynthesis.

We provide an overview of the isotopic signatures of presolar supernova grains, specifically focusing on 44Ti-containing grains with robustly inferred supernova origins and their implications for nucleosynthesis and mixing mechanisms in supernovae. Recent technique advancements have enabled the differentiation between radiogenic (from 44Ti decay) and nonradiogenic 44Ca excesses in presolar grains, made possible by enhanced spatial resolution of Ca-Ti isotope analyses with the Cameca NanoSIMS (Nano-scale Secondary Ion Mass Spectrometer) instrument. Within the context of presolar supernova grain data, we discuss (i) the production of 44Ti in supernovae and the impact of interstellar medium heterogeneities on the galactic chemical evolution of 44Ca/40Ca, (ii) the nucleosynthesis processes of neutron bursts and explosive H-burning in Type II supernovae, and (iii) challenges in identifying the progenitor supernovae for 54Cr-rich presolar nanospinel grains. Drawing on constraints and insights derived from presolar supernova grain data, we also provide an overview of our current understanding of the roles played by various supernova types- including Type II, Type Ia, and electron capture supernovae- in accounting for the diverse array of nucleosynthetic isotopic variations identified in bulk meteorites and meteoritic components. We briefly overview the potential mechanisms that have been proposed to explain these nucleosynthetic variations by describing the transport and distribution of presolar dust carriers in the protoplanetary disk. We highlight existing controversies in the interpretation of presolar grain data and meteoritic nucleosynthetic isotopic variations, while also outlining potential directions for future research.

Land-Use Impacts on Soil Erosion: Geochemical Insights from an Urban Drinking Catchment, South-Central Chile

We investigate the influence of land use and land cover (LU/LC) changes on soil erosion and chemical weathering processes within the Nonguén watershed in the Coastal Cordillera of south-central Chile. The watershed is divided into three sub-basins, each characterized by distinct LU/LC patterns: native forest and exotic plantations. A comprehensive geochemical analysis, including trace elements and lithium (Li) isotopes, was conducted on river water and suspended sediment samples collected from streams within these sub-basins to assess how land management practices, particularly plantation activities, influence the geochemical composition of river systems. Our results show that sub-basins dominated by exotic plantations exhibit significantly higher concentrations of major and trace elements in suspended sediments compared to sub-basins dominated by native forests. The elevated trace element concentrations are primarily attributed to increased physical erosion due to forestry activities such as clear-cutting and soil disturbance, which enhance sediment mobilization. Notably, concentrations of elements such as Fe, Al, and As in plantation-dominated sub-basins are raised to ten times higher than in native-dominated sub-basins. In contrast, sub-basins with native forest cover exhibit lower levels of sediment transport and trace element mobilization, suggesting that native vegetation exerts a stabilizing effect that mitigates soil erosion. Despite the substantial differences in sediment transport and element concentrations, Li isotopic data (δ7Li) show minimal fractionation across the different LU/LC types. This indicates that land use changes impact the chemical weathering processes less compared to physical erosion. The isotopic signatures suggest that physical erosion, rather than chemical weathering, is the dominant process influencing trace element distribution in plantation-dominated areas. The study provides critical insights into how forestry practices, specifically the expansion of exotic plantations, accelerate soil degradation and affect the geochemical composition of river systems. The increased sediment loads, and trace element concentrations observed in plantation-dominated sub-basins, raise concerns about the long-term sustainability of forest management practices, particularly regarding their impacts on water quality in urban catchment areas. These results are of significant relevance for environmental management and policy, as they underscore the need for more investigation and sustainable land use strategies to minimize soil erosion and preserve water resources in regions undergoing rapid LU/LC changes.

Fate of methane in canals draining tropical peatlands.

Tropical wetlands and freshwaters are major contributors to the growing atmospheric methane (CH4) burden. Extensive peatland drainage has lowered CH4 emissions from peat soils in Southeast Asia, but the canals draining these peatlands may be hotspots of CH4 emissions. Alternatively, CH4 oxidation (consumption) by methanotrophic microorganisms may attenuate emissions. Here, we used laboratory experiments and a synoptic survey of the isotopic composition of CH4 in 34 canals across West Kalimantan, Indonesia to quantify the proportion of CH4 that is consumed and therefore not emitted to the atmosphere. We find that CH4 oxidation mitigates 76.4 ± 12.0% of potential canal emissions, reducing emissions by ~70 mg CH4 m-2 d-1. Methane consumption also significantly impacts the stable isotopic fingerprint of canal CH4 emissions. As canals drain over 65% of peatlands in Southeast Asia, our results suggest that CH4 oxidation significantly influences landscape-scale CH4 emissions from these ecosystems.

Composite Mesozoic Carbon and Oxygen Isotope Signals of Selected Events as Encountered in the Southern Tethyan Margin: an Overview

Composite Mesozoic Carbon and Oxygen Isotope Signals of Selected Events as Encountered in the Southern Tethyan Margin: an Overview

Characteristics of carbazole compounds in ultra-deep marine oil from Fuman oilfield, Tarim Basin: Significance for thermal maturity assessment of crude oil

Carbazoles in Ordovician ultra-deep marine oil from the FI17 fault zone in Fuman oilfield (Tarim Basin) were separated using a recently proposed silica gel column chromatographic method and the enriched fractions were analyzed by GC–MS. Biomarker and carbon isotope signatures revealed that all oil in the study area was produced from the same source rock and that compositional differences can be attributed to thermal maturation. The convergent ratios of N-H shielded isomers/N-H half shielded isomers and benzo[a]carbazole/(benzo[a]carbazole + benzo[c]carbazole) suggested that carbazoles in crude oil had not been affected by vertical migration. Therefore, thermal maturity was identified as the main controlling factor affecting chages of carbazole concentrations and ratios in crude oil. The concentrations of the total carbazole and its three isomers (N-H shielded isomers, N-H half shielded isomers and exposed isomers) in crude oil decreased sharply with increasing maturity. The 1,8-dimethylcarbazole/carbazole (1,8-MCa/Ca) and 1,8-dimethylcarbazole/2,4-dimethylcarbazole (1,8-MCa/2,4-MCa) ratios showed significant correlation with maturity expressed as %VRE (the vitrinite reflectance equivalent converted from MPI1 and MPR) when %VRE is <1.2 %. Similar trends were observed in the 1-methylcarbazole/3-methylcarbazole (1-MCa/3-MCa) as well as 1,8-dimethylcarbazole/2,6- dimethylcarbazole (1,8-DMCa/2,6-DMCa), (1,5- dimethylcarbazole + 3-ethylcarbazole)/2, 6-dimethylcarbazole ((1, 5-DMCa + 3-ECa)/2, 6-DMCa), and (1, 4-dimethylcarbazole + 4-ethylcarbazole)/2, 6-dimethylcarbazole ((1, 4-DMCa + 4-ECa)/2, 6-DMCa) when the %VRE of crude oil exceeds 1.0 %. This indicated that the concentrations and ratios of carbazole can be used to qualitatively evaluate crude oil maturity. The ratio of 1,8-dimethylcarbazole/1-ethylcarbazole (1,8-DMCa/1-ECa) showed a strict linear relationship with %VRE. The maturity of marine oil can be calculated using the formulas %Rc (the vitrinite reflectance equivalent calculated from MPI1) = −0.0335(1, 8-DMCa/1-ECa) + 1.2902 or %Rc1 (the vitrinite reflectance equivalent calculated from MPR) = −0.0405 (1, 8-DMCa/1-ECa) + 1.3418. The study can be helpful for exploring ultra-deep hydrocarbons and restoring the thermal history of source rocks in the Tarim Basin.

Molybdenum isotopes demonstrate that multistage upgrading is required to generate heavy rare earth element–enriched carbonatites

Carbonatites with heavy rare earth element (HREE) enrichment are a rare and intriguing prospect for economic geology research, due to the growing global demand for HREEs in various industries. However, debate persists over the mechanism responsible for HREE enrichment in carbonatites, with the mantle source, magmatic-hydrothermal evolution, or a combination of these factors proposed to be responsible. This study examines three adjacent Late Triassic carbonatites (from the Huanglongpu, Huayangchuan, and Jialu carbonatite dike systems) in the Lesser Qinling of Central China and uses Mo isotope systematics to provide unique insights into the HREE enrichment process of these magmas. All three carbonatites exhibit elevated total REE (ΣREE) concentrations (up to 4600 ppm), along with significant HREE enrichment (ΣHREE/ΣREE = 0.1−0.4). Notably, Jialu carbonatite stands out for having the highest total HREE concentrations (≥360 ppm) and ΣHREE/ΣREE ratios (0.2−0.4). Regardless of their variable degrees of HREE enrichment, the three carbonatites display similar Sr-Nd-Pb isotope signatures, which indicates a shared enriched mantle source. The Huanglongpu and Huayangchuan carbonatites mostly display significantly lighter δ98/95Mo (−1.71‰ to −0.15‰) values than the depleted mantle, which indicates an origin from an enriched mantle influenced by recycled pelagic clays and Fe-Mn nodules. Both types of marine sediments are enriched in REEs and would have undergone initial HREE enrichment during slab dehydration and metamorphism, resulting in an HREE-enriched mantle source region. In contrast, Jialu carbonatite possesses significantly heavier δ98/95Mo (0.13‰−1.89‰), which is indicative of the subsequent influence of hydrothermal processes. Additional evidence of this hydrothermal influence at Jialu is preserved in calcite crystal fluid inclusions, elevated δ18O (8.71‰−10.72‰), non-charge-and-radius−controlled (CHARAC) Y/Ho ratios (36−41), and low Sr concentrations (&amp;lt;4800 ppm). Secondary upgrading of HREEs at Jialu occurred due to preferential complexation and transportation during hydrothermal exsolution. This study demonstrates that maximum HREE enrichment in carbonatites is achieved through a two-stage process that involves both a refertilized mantle source and late-stage hydrothermal exsolution.

Predicting oxygen-18 and deuterium over South America: Local Meteoric Water Lines for countries and biogeographical regions

ABSTRACT Rainfall stable isotopes ratios of water, 2H/1H and 18O/16O, play a crucial role as natural tracers through the various compartments of the hydrological cycle in hydrological studies. Knowing the isotopic signatures of precipitation help us to interpret water entry into continental hydrological systems, such as basins and aquifers. Spatial predictions of δ18 O and δ2 H in precipitation across South America were performed using multivariate geostatistics supported by remote sensing covariates. This is the first map dedicated to describing countries and biogeographical region’s spatiotemporal isotopic distributions with their Local Meteoric Water Lines (LMWL). R2 from 0.90 to 0.99 were found considering all LMWLs. Historical, May-September, and October-April periods modeling errors are 2.83, 2.41, and 2.67% for δ2 H, and 0.33, 0.37, and 0.41% for δ18 O, respectively.

Discriminative characteristics of hydrochemical components and sedimentary organic matter in Korean coastal aquaculture systems during summer

Understanding the spatial distribution and sources of sedimentary organic matter (OM) in coastal environments is crucial for effective water quality management and the preservation of ecosystem health. Although extensive research has been conducted on OM dynamics, there remains a gap in understanding the ongoing biogeochemical processes in Korean coastal aquaculture zones, particularly during the summer season. To address this gap, we investigated the spatial variation of water chemical properties and isotopic composition of sedimentary OM to trace the composition, source, and reactivity of mixed OM in aquaculture systems along the Korean coast during the summer season. The isotopic approach was applied to surface sediments from five sections: western (W)-1, W-2, southern (S)-1, S-2, and eastern (E)-1. With respect to increased nutrients (mainly nitrate; 1.2 ± 0.6 mg/L) by dam-water discharge near W sections, our isotopic signatures revealed that a substantial fraction of sedimentary OM might dominantly originated from autochthonous OM source (algae; 36.5%) related to the increase of terrestrial nutrients. Simultaneously, the deposition of allochthonous OM (aquacultural feces; 44%) was predominant in the S-2 sections. The 34S-depleted patterns (approximately -7.2‰) in the S-2 section was indicative of active sulfate reduction occurring at the sedimentary boundary. Therefore, together with the precise determination of ongoing OM, our isotopic results provide valuable insights for effectively managing water-sedimentary qualities under the increase of anthropogenic contamination.

Conspicuous parasite modifies appearance and energetics of a marine copepod

Abstract Parasitism is an important driver of ecosystem processes. Copepods are fundamental trophic links in marine food webs and harbour many microeukaryotic parasites, but unreliable access to infected individuals limits quantitative studies of parasite infection costs. Calanus spp., (helgolandicus or finmarchicus), infected with the Yellow-Hyphal Parasite become pigmented and are found near the surface, suggesting predator-mediated dispersal. Conventional markers prevented phylogenetic inference but confirmed that the parasite is not Ichthyophonus hoferi, as previously thought. We identified the pigments, quantified the pigment content and respiration rate, and derived stable isotope signatures of infected and uninfected Calanus spp. to examine costs of infection. We found that the pigments were astaxanthin and β-carotene, associated with the host and parasite, respectively. Parasitized hosts had increased astaxanthin content, reduced respiration rate, and lower lipid content. Ultrastructure imaging revealed parasitic cells associated with lipids in the haemocoel. The changes to host phenotype have detrimental impacts on energetics and the ecology of Calanus. We discuss the role of pigments in parasite-host interactions and suggest that the parasite produces β-carotene pigment for its physiological benefits. The trade-off between physiological benefits of pigments and conspicuousness for parasites is relevant in zooplankton-host systems, as zooplankton rely heavily on transparency for survival.

Contact metamorphism and dolomitization overprint on Cambrian carbonates from the Ossa-Morena Zone (SW Iberian Massif): implications to Sr-chronology of carbonate rocks

AbstractThe Cambrian Series 2 Carbonate Formation from the Alter do Chão Elvas-Cumbres Mayores unit (Ossa-Morena Zone, SW Iberian Massif) is composed of regionally metamorphosed marbles and marlstones that underwent chlorite zone metamorphism and preserve the primaeval limestone 87Sr/86Sr ratios (0.7083–0.7088). These are consistent with the established Lower Cambrian seawater curve, and therefore used for age constraints in formations lacking fossil contents. The regional mineralogical and Sr-isotopic features of the carbonate rocks are frequently overprinted by the effects of contact metamorphism induced by magmatic bodies emplaced during rift-related and synorogenic events of the Palaeozoic, as well as by post-metamorphic dolomitization processes. The development of calc-silicate minerals due to contact metamorphism is common in the rocks of the Carbonate Formation and apparently results from the interaction of the protolith with fluids of different origin: (i) internally produced fluids released by conductive heating (observed in external contact aureoles) and (ii) external intrusion-expelled fluids that, besides leading to the appearance of distinctive assemblages, also promote an influx of strontium content (observed in roof pendants). Calc-silicate mineralogy varies substantially throughout the region, likely due to the heterogeneous distribution of silicate minerals of the protolith, progression of intrusion-driven fluids, and the irregular effect of thermal gradients. Results suggest that high-grade contact metamorphism (hornblende facies or higher) and dolomitization processes imposed on the Carbonate Formation significantly influence the isotopic signatures of the carbonates, providing limitations in applying Sr-isotopic chronology. Graphical abstract

Stable Isotope Analysis of Planktonic Lower Food Webs of Lakes Erie, Huron, Michigan and Superior

Historical plankton samples from the St. Lawrence Great Lakes were subjected to taxon-specific 15N analysis to test the hypothesis that the changes recorded in zooplankton communities during the 21st Century are related to changes in the trophic positions of large-bodied carnivorous copepods. Daphnia mendotae was used as the reference herbivore for trophic-level comparisons. The results were that Limnocalanus macrurus, Diaptomus (Leptodiaptomus) sicilis as well as the cladoceran Bythotrephes cederstroemi show evidence of elevated carnivory compared to data from the 20th Century. The large diaptomid Diaptomus (Leptodiaptomus) sicilis has a stable isotope signature that is significantly more carnivorous in Lake Superior than in Lakes Michigan and Huron by approximately one-half trophic level. Differences were found in 10 cases out of 15 for Limnocalanus (Huron, Michigan Superior), 6 cases out of 15 for Diaptomus (Huron, Michigan) and in 1 out of 1 for Senecella (Superior). We did not find evidence to support the theory that large-bodied calanoid copepods may have improved their representation in the food webs of the upper Great Lakes by shifting their trophic position downward. Instead, large-bodied Calanoida have increased their trophic positions in parallel with their increased relative abundance. More research is thus needed to explain the driving forces for changing food web dynamics in the Great Lakes.

Simulation of Space Charge Effects in Fourier Transform Quadrupole Ion Traps (FT-QITs).

We present ion dynamics simulations regarding the effect of space charge on the performance of Fourier transform quadrupole ion traps (FT-QITs) with special attention to signal stability, mass resolving power, and sensitivity. Ion trajectory simulations within an idealized QIT geometry are performed by applying a dedicated application (QITSim) using an in-house developed open simulation framework (IDSimF). Image current detection transients are generated by the application and are subsequently transformed into frequency spectra of ion secular motion. Such frequency spectra are the basis for the calculation of mass spectra in FT-QIT instruments. The simulation results are used to assess the extent of space charge induced effects regarding the analytical performance of FT-QIT systems. The simulation results for two Cl+ and seven Xe+ isotope ions exhibit diverse space charge induced phenomena. Most prominently, complete isotope signal fusion, quantitative individual signal suppression, and severe signal distortions are observed even at low absolute numbers of trapped ions. Furthermore, significant shifts of the secular oscillation frequencies occur, even when the signal shape appears to be mostly unaffected and when the frequency separation for trapped ions with different masses is large. This significantly limits the applicability of FT-QIT systems for high resolution mass spectrometry. An increase of the RF amplitude of the trapping field as well as increasing the extent of ion excitation partly mitigate these adverse space charge effects; nevertheless, the usable operational range of the simulated FT-QIT system for analytical applications remains rather narrow.

Stable silicon isotope fractionation reflects the routing of water through a mesoscale hillslope

Concentration - isotope Ratio - Discharge (C-R-Q) relationships offer a promising means of disentangling the underlying hydrologic, geochemical, and ecological factors that produce variations in stream solute chemistry across a variety of critical zone systems. However, natural environments are both temporally and spatially complex, and prevailing interpretations of these C-R-Q patterns remain difficult to validate. Here we employ three replicate artificially constructed hillslopes at the Landscape Evolution Observatory (LEO) in Tucson, Arizona as simplified analogs to natural catchments. LEO allows us to record silicon stable isotope (δ30Si) signatures of fluid discharge under a controlled irrigation schedule in a system devoid of vegetation. This unique meso‑scale experiment enables, for the first time, evaluation of metalloid stable isotope signatures at the scale of natural hillslopes constrained to known fluid transit time distributions (TTDs) and limited to fractionation in association with secondary mineral formation. We report δ30Si in discharge samples collected over three randomized storm events of varying intensity. The data reflect consistent enrichment in the fluid phase between +1.00 and +2.07 ‰ across the three hillslopes, despite highly variable irrigation scenarios, reflecting substantial loss of SiO2 from solution due to secondary mineral precipitation. We compare results from an isotope-enabled Reactive Transport Model (RTM) and the discharge measurements from LEO to constrain the contributions of both characteristic watershed TTDs and fractionation pathways in emergent δ30Si signatures. Our study confirms and expands upon recent work in natural systems attributing intra-site variability in silicon stable isotope signatures to the routing of fluid through catchments.

Deep mantle plumes feeding periodic alignments of asthenospheric fingers beneath the central and southern Atlantic Ocean

High-resolution full waveform seismic tomography of the Earth's mantle beneath the south and central Atlantic Ocean brings into focus a series of asthenospheric low shear velocity channels, or "fingers" on both sides of the southern and central mid-Atlantic ridge (MAR), elongated in the direction of absolute plate motion with a spacing of [Formula: see text]1,800 to 2,000 km, and associated with bands of shallower residual seafloor depth anomalies that suggest channeled flow over thousands of kilometers. Each of the three most clearly resolved fingers on the African side of the MAR corresponds to a separate group of whole mantle plumes rooted in distinct patches at the core-mantle boundary, feeding hotspots, and volcanic lines with distinct isotopic signatures. Plumes of a given group appear to merge at the top of the lower mantle before separating again, suggesting interaction of deep mantle flow with a more vigorous mesoscale circulation in the upper mantle. The corresponding hotspots are generally offset from the location of the deep mantle plume roots. The distinct isotopic signatures of these hotspot groups are also detected in the mid-ocean ridge basalts at the location where the fingers meet the ridge. Meanwhile, at least some of the variability within each plume group could originate in the upper mantle and extended transition zone where plumes in a given group appear to merge and pond. This study also adds to mounting evidence that the African large low shear velocity province is not a uniform, unbroken pile of dense material rising high above the core-mantle boundary, but rather a collection of mantle plumes rooted in patches of distinct composition.

Using mercury and lead stable isotopes to assess mercury, lead, and trace metal source contributions to Great Salt Lake, Utah, USA

Great Salt Lake is a critical habitat for migratory birds that is threatened by elevated metal concentrations, including mercury (Hg) and lead (Pb), and is subject to severe hydrologic changes, such as declining lake level. When assessing metal profiles recorded in Great Salt Lake sediment, a large data gap exists regarding the sources of metals within the system, which is complicated by various source inputs to the lake and complex biogeochemistry. Here, we leverage Hg and Pb stable isotopes to track relative changes in metal source contributions to Great Salt Lake over time. Mercury and Pb concentrations increase in sediments deposited after 1920 and peak between 1965 and 1995, following closure of several local smelters and the onset of increased emission controls. The nominal associations above are confirmed via Hg stable isotopes in pre-1920 background sediments, which reflect atmospheric inputs from regional and global origin, whereas Hg and Pb stable isotopes together indicate that elevated metal concentrations in mid-late 20th century sediments reflect increased mining/smelting inputs. The observed minimal rebound towards pre-1920 Pb isotope signatures in 21st century sediments indicates that mining/smelting inputs, though reduced, remain a primary source of Pb to Great Salt Lake. In contrast, the more pronounced rebound of Hg stable isotope signatures to pre-1920 values indicate a greater contribution of atmospheric inputs of regional/global origin to current Hg inputs, though Hg concentrations are ~10 times greater than pre-1920 background values due to global increases in atmospheric Hg concentrations or possibly slow recovery from local contamination. The importance of regional/global Hg sources to the system suggests that reductions in Hg bioaccumulation in the open water food webs of Great Salt Lake are more dependent on national and global reductions in Hg emissions and management strategies to limit methylmercury production within system. This work highlights the utility of using coupled Hg and Pb stable isotope values to assess trace metal pollution sources and pathways in aquatic systems.

Impact of submarine volcanic versus hydrothermal activity onto the strontium and lithium isotopic signatures of the water column (TONGA)

During the TONGA cruise (2019), seawater samples were collected to assess the effect of volcanic eruption versus submarine hydrothermal system on the water column. For this purpose, two locations were investigated, the first one located directly under the influence of the New Late’iki island (eruption in October 2019), and the second one showing ongoing submarine hydrothermal activity. At both locations, the total strontium (TSr) and lithium (TLi) concentrations vary between 94.4 and 152.3 µmol/L and 13.2 and 203.5 µmol/L, respectively. When combined, TSr and TLi concentrations of all samples in the water column are higher than those of the oligotrophic water. Both volcanic eruption and submarine hydrothermal activity (e.g. volcanic ashes, particles, gas condensate) can deliver substantial amount of TSr and TLi to the water column. The distribution of TSr versus TLi evidences linear trends either with a negative or positive slope. The negative correlation is observed in the water column at both sites, directly under the influence of the eruption and in the vicinity of the volcano with hydrothermal activity. The positive TSr versus TLi correlation is observed at site under submarine hydrothermal influence and is in line with black smokers related hydrothermal plumes. The 87Sr/86Sr ratios vary between 0.709147 and 0.709210 and δ7Li values vary between +10.1 and +37.6 ‰. While 92% of the measured 87Sr/86Sr ratios are in line with the mean value of oligotrophic waters, once combined with the δ7Li values, only 20% of them remains within this field. The wide range of δ7Li values decreases from sea-surface down to ~140 mbsl, before increasing at greater depth, while defining different linear trend according to the dissolved inorganic carbon concentrations. The variability of δ7Li values reflect hydrothermal contribution, mineral–seawater interaction and potentially biology–environment interaction. In the particular geological setting of the study, where both hydrothermal and volcanic activities were at play, disentangling both contributions on water column implies a combined use of elemental and isotopic signatures of Sr and Li tracers.

Porphyry copper formation driven by water-fluxed crustal melting during flat-slab subduction

AbstractThe prevailing view of the formation of porphyry copper deposits along convergent plate boundaries involves deep crustal differentiation of metal-bearing juvenile magmas derived from the mantle wedge above a subduction zone. However, many major porphyry districts formed during periods of flat-slab subduction when the mantle wedge would have been reduced or absent, leaving the source of the ore-forming magmas unclear. Here we use geochronology and thermobarometry to investigate deep crustal processes during the genesis of the Late Cretaceous–Palaeocene Laramide Porphyry Province in Arizona, which formed during flat-slab subduction of the Farallon Plate beneath North America. We show that the isotopic signatures of Laramide granitic rocks are consistent with a Proterozoic crustal source that was potentially pre-enriched in copper. This source underwent water-fluxed melting between 73 and 60 Ma, coincident with the peak of granitic magmatism (78–50 Ma), porphyry genesis (73–56 Ma) and flat-slab subduction (70–40 Ma). To explain the formation of the Laramide Porphyry Province, we propose that volatiles derived from the leading edge of the Farallon flat slab promoted melting of both mafic and felsic pre-enriched lower crust, without requiring extensive magmatic or metallogenic input from the mantle wedge. Other convergent plate boundaries with flat-slab regimes may undergo a similar mechanism of volatile-mediated lower-crustal melting.

Desert dust improves the photophysiology of heat-stressed corals beyond iron

Desert dust is an important source of essential metals for marine primary productivity, especially in oligotrophic systems surrounded by deserts, such as the Red Sea. However, there are very few studies on the effects of dust on reef-building corals and none on the response of corals to heat stress. We therefore supplied dust to two coral species (Stylophora pistillata and Turbinaria reniformis) kept under control conditions (26 °C) or heat stress (32 °C). Since dust releases large amounts of iron (Fe) in seawater, among other metals, the direct effect of different forms of Fe enrichment on coral photosynthesis was also tested. First, our results show that the desert dust altered the coral metallome by increasing the content of metals that are important for coral physiology (e.g. lithium (up to 5-fold), manganese (up to 4-fold in S. pistillata), iron (up to 3-fold in S. pistillata), magnesium (up to 1.3-fold), molybdenum (up to 1.5-fold in S. pistillata)). Overall, metal enrichment improved the photosynthetic performance of corals, especially under thermal stress (e.g. Pgross (up to 2-fold), Pnet (up to 10-fold), chlorophyll (up to 1.5-fold), symbionts (up to 1.6-fold)). However, Fe exposure (ferric chloride or ferric citrate) did not directly improve photosynthesis, suggesting that it is the combination of metals released by the dust, the so-called “metal cocktail effect”, that has a positive impact on coral photophysiology. Dust also led to a decrease in Ni uptake (up to 1.4-fold in the symbionts), likely related to the nitrogen metabolism. Finally, we found that the isotopic signature of metals such as iron, zinc and copper is a good indicator of heat stress and dust exposure in corals. In conclusion, desert dust can increase coral resistance to bleaching by supplying corals with essential metals.