Isotope Fractionation Research Articles

Zinc isotope fractionation during the sorption of Zn to minerals and organic matter in sediment cores affected by anthropogenic pollution

Zinc stable isotopes (δ66Zn) serve as a widely fingerprinting tool for detecting anthropogenic Zn contamination. However, there is a limited understanding of δ66Zn behavior during the sorption of Zn to minerals and organic matter. In this study, we have determined the δ66Zn values in specific fractions to investigate their effectiveness in tracing anthropogenic Zn. The revised Community Bureau of Reference (BCR) extraction procedure was applied to a coastal marine core from Osaka Bay and from a lacustrine core from Lake Biwa, both with a history of anthropogenic metal pollution. The δ66Zn values varied from −0.14 ‰ to +1.00 ‰ across the four to five chemical fractions with up to 0.9 ‰ variation within a single horizon. The highest δ66Zn values in the acid-soluble fraction (up to +1.00 ‰) could be explained by the preferential sorption of 66Zn to carbonates and/or the preferential incorporation of 66Zn into calcite. The complex isotopic fractionation during the sorption of Zn to and co-precipitation with Fe–Mn oxyhydroxides likely resulted in an unclear pattern of the δ66Zn values of the reducible fraction. Low δ66Zn values in the oxidizable fraction (Osaka Bay) agree with the 64Zn enrichment in phytoplankton. Higher δ66Zn values of the reducible and oxidizable fractions of the Lake Biwa core indicate that environmental conditions (e.g. ionic strength) and for instance different phytoplankton species or dissolved and suspended particulate matter input drive the Zn isotope fractionation depending on the system (marine vs. lacustrine). The δ66Zn values of the acid-soluble fraction (Osaka Bay and Lake Biwa), of the reducible fraction (only Lake Biwa) and of oxidizable fraction (only Osaka Bay) better reflected the temporal changes in the Zn concentration than the bulk sediment, indicating that these fractions could be a sensitive fingerprinting tool for anthropogenic Zn contamination.

Early planetesimal differentiation and late accretion shaped Earth's nitrogen budget.

The relative roles of protoplanetary differentiation versus late accretion in establishing Earth's life-essential volatile element inventory are being hotly debated. To address this issue, we employ first-principles calculations to investigate nitrogen (N) isotope fractionation during Earth's accretion and differentiation. We find that segregation of an iron core would enrich heavy N isotopes in the residual silicate, while evaporation within a H2-dominated nebular gas produces an enrichment of light N isotope in the planetesimals. The combined effect of early planetesimal evaporation followed by core formation enriches the bulk silicate Earth in light N isotopes. If Earth is comprised primarily of enstatite-chondrite-like material, as indicated by other isotope systems, then late accretion of carbonaceous-chondrite-like material must contribute ~ 30-100% of the N budget in present-day bulk silicate Earth. However, mass balance using N isotope constraints shows that the late veneer contributes only a limited amount of other volatile elements (e.g., H, S, and C) to Earth.

Geographical origin traceability of sweet cherry (Prunus avium (L.) Moench) in China using stable isotope and multi-element analysis with multivariate modeling

The deliberately origin mislabeling of sweet cherry causes significantly disruptions to market integrity and consumers' trust. In this study, 153 cherry samples from five provinces in China and the corresponding irrigation water and soil samples were collected. 5 stable isotope ratios (δ13C, δ15N, δ2H, δ18O, 87Sr/86Sr) and 8 multi-element contents (Na, Mg, P, K, Ca, Fe, Zn, Se) of cherry were determined by EA-IRMS and ICP-MS to study isotopic fractionation and elemental enrichment mechanisms for origin traceability. The results show the δ2H and δ18O of cherry exhibit a strong correlated with its irrigation water (r2 > 0.85), while δ15N, 87Sr/86Sr, Fe, Zn and Se contents are related to its cultivated soil (r2 > 0.75), and the δ13C is related to the local microclimate. ANOVA reveals that the regional differences of δ13C, δ2H, δ18O, 87Sr/86Sr as well as Na, Mg, Ca contents of cherry are significant (P < 0.05), and are important geographical indicators. Various multivariate modeling methods, HCA, PLS-DA, and LDA, were employed with the overall accuracy exceeding 90%. This strategy provides an effective mean to verify the label authenticity of cherry origin in Chinese market.

Sources and processes affecting the abundances of atmospheric NHx using δ15N over northwestern Indo-Gangetic plain

Ammonia (NH3) is the major constituent among all the reactive nitrogen species present in the atmosphere, and the most essential species for secondary inorganic aerosol formation. Recent satellite-based observations have identified the Indo-Gangetic Plain (IGP) as a major hotspot of global NH3 emission; however, the major sources and atmospheric processes affecting its abundance are poorly understood. The present study aims to understand the wintertime sources of NH3 over a semi-urban site (Patiala, 30.3°N, 76.4°E, 249 m amsl) located in the IGP using species specific δ15N in PM2.5. A distinct diurnal variation in the stable isotopic signature of total nitrogen (δ15N-TN) and ammonium (δ15N–NH4+) were observed; although, average day and night time concentrations of TN and NH4+ were similar. Mixing model results using δ15N–NH3 reveal the dominance of non-agricultural emissions (NH3 slip: 47 ± 24%) over agricultural emissions (24 ± 11%), combustion sources (19 ± 14 %), and biomass burning (10 ± 8%) for atmospheric NH3. Diurnal variability in source contributions to NH3 was insignificant. Further, significantly negative correlations of δ15N–NH4+ with ambient relative humidity (RH) and daytime NO3−-N concentration were observed, and attributed to the possibility of NH4NO3 volatilization during day-time owing to lower RH and higher temperature, resulting in isotopic enrichment of the remaining NH4+ in aerosol phase. This study, a first of its type from India, highlights the importance of non-agricultural NH3 emissions over the agriculture dominated IGP region, and the role of local meteorology on the isotopic fractionation of δ15N in aerosol NH4+.

Quantifying Nitrogen Treatment by an In-stream Bioreactor in a Watershed Served by Septic Systems

Septic systems are potentially significant sources of nitrogen to groundwater and surface water. In-stream practices, such as in-stream bioreactors (IBRs), that promote or enhance nitrogen treatment are promising solutions to reduce nitrogen loads to nutrient-sensitive water. More work is needed to evaluate the efficiency of IBRs in new applications, such as residential sub-watersheds with a high-density of septic systems. The goal of this study was to quantify nitrogen treatment by an in-stream bioreactor (IBR) during baseflow conditions. The IBR was constructed in March 2017 when approximately 1 m of streambed sediment was excavated and backfilled with 0.75 m of woodchips capped by 0.2 m of rotary-kiln, expanded slate and boulder-sized riprap. Samples were collected monthly from July 2017 – March 2019 including IBR inflow, monitoring ports within the IBR, groundwater seeps draining to the IBR, and IBR outflow. Water samples were analyzed for total dissolved nitrogen (TDN), nitrate, ammonium, dissolved organic carbon, chloride, and nitrate isotopic fractionation. The IBR reduced the median concentration of TDN and nitrate by 40% and 77%, respectively. The median mass removal of TDN and nitrate was 26 and 5.2 g day− 1, respectively. Nitrogen-chloride ratios and isotopic fractionation data suggest that denitrification was likely a predominant nitrogen reduction mechanism. In addition to nitrogen treatment, the IBR provided other benefits by improving erosion control, streambank stabilization, and increased bank-full storage from 6 m3 to 19.2 m3. Results indicated that the IBR improved water quality and other residential sub-watersheds with septic systems would benefit from similar practices.

Comparison of δ13C and δ15N of ecologically relevant amino acids among beluga whale tissues

Ecological applications of compound-specific stable isotope analysis (CSIA) of amino acids (AAs) include 1) tracking carbon pathways in food webs using essential AA (AAESS) δ13C values, and 2) estimating consumer trophic position (TP) by comparing relative differences of ‘trophic’ and ‘source’ AA δ15N values. Despite the significance of these applications, few studies have examined AA-specific SI patterns among tissues with different AA compositions and metabolism/turnover rates, which could cause differential drawdown of body AA pools and impart tissue-specific isotopic fractionation. To address this knowledge gap, especially in the absence of controlled diet studies examining this issue in captive marine mammals, we used a paired-sample design to compare δ13C and δ15N values of 11 AAs in commonly sampled tissues (skin, muscle, and dentine) from wild beluga whales (Delphinapterus leucas). δ13C of two AAs, glutamic acid/glutamine (Glx, a non-essential AA) and, notably, threonine (an essential AA), differed between skin and muscle. Furthermore, δ15N of three AAs (alanine, glycine, and proline) differed significantly among the three tissues, with glycine δ15N differences of approximately 10 ‰ among tissues supporting recent findings it is unsuitable as a source AA. Significant δ15N differences in AAs such as proline, a trophic AA used as an alternative to Glx in TP estimation, highlight tissue selection as a potential source of error in ecological applications of CSIA-AA. Amino acids that differed among tissues play key roles in metabolic pathways (e.g., ketogenic and gluconeogenic AAs), pointing to potential physiological applications of CSIA-AA in studies of free-ranging animals. These findings underscore the complexity of isotopic dynamics within tissues and emphasize the need for a nuanced approach when applying CSIA-AA in ecological research.

Leaf wax n-alkane distribution and hydrogen isotopic fractionation in fen plant communities of two Mediterranean wetlands (Tenaghi Philippon, Nisí fen—Greece)

Many continental paleoclimate archives originate from wetland sedimentary sequences. While several studies have investigated biomarkers derived from peat-generating vegetation typical of temperate/boreal bogs (e.g., Sphagnum), only scant information is available on emergent plants predominant in temperate/subtropical coastal marshlands, peri-lacustrine and fen environments. Here, we address this gap, focusing on two wetlands in the Mediterranean (Nisí fen and Tenaghi Philippon, Greece). We examined the concentration, homologue distribution, and hydrogen stable isotopic composition (δ2H) of leaf wax n-alkanes in 13 fen plant species, their surrounding soil, and surface water during the wet growing season (spring) and the declining water table period (summer). Our findings indicate that local graminoid species primarily contribute to the soil n-alkane signal, with a lesser influence from forbs, likely owing to differences in morphology and vegetation structure. The δ2H values of surface and soil water align with local average annual precipitation δ2H, reflecting winter-spring precipitation. Consistently, the average δ2H of local surface, soil, and lower stem water showed negligible evaporative enrichment, confirming minimal 2H-fractionation during water uptake. We find that δ2H values of source water for wax compound synthesis in local fen plants accurately mirror local annual precipitation. Furthermore, despite differences between leaves and lower stems in n-alkane production rates, their δ2H values exhibit remarkable similarity, indicating a shared metabolic substrate, likely originating in leaves. Our net 2H-fractionation values (i.e., precipitation to leaf n-alkanes) align with those in Chinese highlands and other similar environments, suggesting consistency across diverse climatic zones. Notably, our data reveal a seasonal decrease in the carbon preference index (CPI) in plant samples, indicating wax lipid synthesis changes associated with increased aridity. Additionally, we introduce a new parity isotopic difference index (PID) based on the consistent δ2H difference between odd and even n-alkane homologues. The PID demonstrates a strong anticorrelation with plant CPI, suggesting a potential avenue to trace long-term aridity shifts through δ2H analysis of odd and even n-alkane homologues in sedimentary archives. While further development of the PID is necessary for broad application, these findings highlight the intricate interplay between plant physiology, environmental parameters, and sedimentary n-alkanes in unravelling past climatic conditions.

Oxygen Isotopologues Resolved from Water Oxidation Electrocatalysis by Electron Paramagnetic Resonance Spectroscopy.

Electrocatalytic water oxidation is a key transformation in many strategies designed to harness solar energy and store it as chemical fuels. Understanding the mechanism(s) of the best electrocatalysts for water oxidation has been a fundamental chemical challenge for decades. Here, we quantitate evolved dioxygen isotopologue composition via gas-phase EPR spectroscopy to elucidate the mechanisms of water oxidation on metal oxide electrocatalysts with high precision. Isotope fractionation is paired with computational and kinetic modeling, showing that this technique is sensitive enough to differentiate O-O bond-forming steps. Strong agreement between experiment and theory indicates that for the nickel-iron layered double hydroxide─one of the best earth-abundant electrocatalysts to be studied─water oxidation proceeds via a dioxo coupling mechanism to form a side-bound peroxide rather than a hydroxide attack to form an end-bound peroxide.

Elemental and oxygen isotopic fractionation recorded in highly vaporized cosmic spherules from Widerøefjellet, Sør Rondane Mountains (East Antarctica)

AbstractUpon passage through Earth's atmosphere, micrometeorites undergo variable degrees of melting and evaporation. Among the various textural and chemical groups recognized among cosmic spherules, that is, melted micrometeorites, a subset of particles may indicate anomalously high degrees of vaporization based on their chemical and isotopic properties. Here, a selection of such refractory element‐enriched cosmic spherules from Widerøefjellet (Sør Rondane Mountains, East Antarctica) is characterized for their petrographic features, major and trace element concentrations (N = 35), and oxygen isotopic compositions (N = 23). Following chemical classification, the highly vaporized particles can be assigned to either the “CAT‐like” or the “High Ca‐Al” cosmic spherule groups. However, through the combination of major and trace element concentrations and oxygen isotopic data, a larger diversity of processes and precursor materials are identified that lead to the final compositions of refractory element‐enriched particles. These include fragmentation, disproportional sampling of specific mineral constituents, differential melting, metal bead extraction, redox shifts, and evaporation. Based on specific element concentrations (e.g., Sc, Zr, Eu, Tm) and ratios (e.g., Fe/Mg, CaO + Al2O3/Sc + Y + Zr + Hf), and variations of O isotope compositions, “CAT‐like” and “High Ca‐Al” cosmic spherules likely represent a continuum between mineral endmembers from both primitive and differentiated parent bodies that experienced variable degrees of evaporation.

Continuous-Flow Stable Sulfur Isotope Analysis of Organic and Inorganic Compounds by EA-MC-ICPMS.

Elemental analysis (EA) coupled to isotope ratio mass spectrometry (IRMS) is a well-established method to derive stable isotope ratios of sulfur (34S/32S). Conversion of sulfur to SO2 by EA and measurement of SO2 isotopologues by IRMS represents the simplest and most versatile method to accomplish isotope measurement of sulfur even in bulk samples. Yet, interferences by oxygen isotopes in SO2 often impair the precision and trueness of measured results. In the current study, we coupled EA to multicollector inductively coupled plasma mass spectrometry (MC-ICPMS) to establish a method that avoids such interferences due to direct measurement of S+ ions. In addition, measurement of the 33S/32S isotope ratios is possible, thus representing the first bulk method that is suitable to study mass-independent isotope fractionation (MIF). Analytical precision (σ) of available Ag2S and BaSO4 reference materials (RMs) was, on average, 0.2 mUr for δ33S and δ34S, never exceeding 0.3 mUr within this study (1 mUr = 1‰ = 0.001). Measured δ34S values of reference materials agreed within ±0.2 mUr of officially reported values. Measurement of wood samples yielded good precision (0.2 mUr) for sulfur amounts as low as 3.5 μg, but precision deteriorated for samples at lower sulfur contents due to poor peak shape. Finally, we explored cross-calibration of organic liquids separated via gas chromatography (GC) against solid RMs combusted via EA that avoids challenging offline conversion of RMs. Results indicate good precision (≤0.08 mUr) and acceptable trueness (≤0.34 mUr) for determination of δ34S, demonstrating the future potential of such an approach.

Calcium isotopic composition of the bulk silicate Earth: A komatiite perspective

Calcium (Ca) isotopic composition of the mantle has been previously estimated as δ44/40Ca. However, δ44/40Ca of the mantle records both its stable isotopic composition and excess/deficit in radiogenic 40Ca that can be produced by the decay of 40K. Here, we present the high-precision Ca isotopic compositions of 16 Archean komatiites from five representative localities (Barberton, Munro, Abitibi, Yilgarn, and Taishan). Due to the high degrees of partial melting that led to their formation, these komatiites are used here to simultaneously estimate ε40/44Ca, δ44/40Ca, and δ44/42Ca of the bulk silicate Earth. The komatiites exhibit a resolvable negative ε40/44Ca relative to SRM915a, with an average of −0.6 ± 0.1 (2SE, 95 c.i.% if not specified). Given the lack of significant differences among the samples and the non-zero value of ε40/44Ca, we suggest using δ44/42Ca to report the stable Ca isotopic composition in this study. Excluding one sample (SD6/400), which may have been affected by alteration, the remaining komatiites display relatively homogeneous δ44/42Ca, ranging from 0.39 ± 0.02‰ (2SE, N = 16) to 0.49 ± 0.02‰ (2SE, N = 10), defining a mean of 0.44 ± 0.02‰ (2SE, N = 15). The absence of correlations between δ44/42Ca and LOI, Sr/Nd, (Dy/Yb)N, and (La/Sm)N among the komatiites indicates that post-eruption alteration, the influence of residual garnet, as well as prior melt extraction from the mantle source have had a negligible influence on their stable Ca isotopic compositions. Based on available experimental petrological data and isotope fractionation factors, it is demonstrated that komatiites were insignificantly fractionated from their mantle sources (i.e., <0.02% in δ44/42Ca). Their δ44/42Ca represents the ambient mantle at the time of segregation. Accordingly, we suggest that the average δ44/42Ca and ε40/44Ca of the komatiites measured here are representative of the bulk silicate Earth. Our new estimate can serve as a reference point for Ca isotopes as a two-dimensional tracer for sources and geological processes.

Tl, Mo and U isotopes in U-ore deposits record Earth's fundamental redox processes

Understanding changes in redox conditions in the Earth's geological record is fundamental to unravelling some of the major events of our planet's history, such as the Great Oxidation Event (G.O.E.), biological changes through time related to mass extinctions, or the formation of ore deposits for primordial metal resources. Rocks from uranium deposits are ideal candidates to examine the coupled isotopic fractionation of Tl, Mo and U, as they are fundamentally caused by redox processes, occur in a wide variety of geological settings throughout much of geological history (from about 3 Ga), and result from the interplay between fluids and rocks of variable redox states. Herein we measure δ97Mo (−10.2 to +6.1 ‰), ε205Tl (−9.5 to +5.0 ε-units), and δ238U (−0.72 to 0.30 ‰) for 34 samples from granite-related, intrusive, metamorphic, and Proterozoic unconformity related U deposits. Collectively, these results suggest: 1) in metamorphic and unconformity-related contexts, samples with decreasing ε205Tl values also have decreasing δ238U values, indicative of change in redox conditions, 2) ε205Tl values in the sulfide-rich samples likely reflect the affinity of 205Tl for these minerals, 3) Tl undergoes significant isotopic fractionation during the reduction of U-bearing fluids to precipitate uraninite, and 4) Tl isotopes do not fractionate during secondary remobilization of elements within these systems, and thus retain a record of the conditions of formation, whereas Mo isotopes are heavily fractionated by secondary remobilization. We suggest that the study of U, Mo, and Tl isotopes in U-ore deposits conveys new information related to building blocks of life on Earth and shows great potential for the study of past oxygenation events, thus potentially allowing us to reconstruct the geological and chemical history of our planet.

Antimony isotopic fractionation induced by Sb(V) adsorption on β-MnO2

Antimony (Sb) isotopes hold immense promise for unraveling Sb biogeochemical cycling in environmental systems. Mn oxides help control the fate of Sb via adsorption reactions, yet the behavior and mechanisms of Sb isotopic fractionation on Mn oxides are poorly understood. In this study, we examine the Sb isotopic fractionation induced by adsorption on β-MnO2 in different experiments (kinetic, isothermal, effect of pH). We observe that adsorption on β-MnO2 surfaces preferentially enriches lighter Sb isotopes through equilibrium fractionation, with Δ123Sbaqueous-adsorbed of 0.55–0.79 ‰. Neither the pH or surface coverage affects the fractionation magnitude. The analysis of extended X-ray absorption fine structure (EXAFS) demonstrates that the enrichment of light isotope results from the adsorption of inner-sphere complexation on solids. Our finding of this study enhances our comprehension of the impact of β-MnO2 on Sb isotopic fractionation behavior and mechanism and facilitate the applicability of Sb isotopes as effective tracers to elucidate the origins and pathways of Sb contamination in environmental systems, as well as provide a new insight into forecasting the isotopic fractionation of other similar metals adsorbed by manganese oxides.

Synthesis of 13C-depleted organic matter from CO in a reducing early Martian atmosphere

Organic matter found in early Martian sediment may yield clues to the planet’s environmental conditions, prebiotic chemistry and habitability, but its origin remains unclear. Strong 13C depletion in sedimentary organic matter at Gale crater was recently detected by the Curiosity rover. Although this enigmatic depletion remains debated, if correct, a mechanism to cause such strong 13C depletion is required. Here we show from CO2 photolysis experiments and theoretical considerations that solar ultraviolet photolysis of CO2 in a reducing atmosphere can yield strongly 13C-depleted CO. We suggest that atmospheric synthesis of organic compounds from photolysis-produced CO is a plausible mechanism to explain the source of isotopically depleted organic matter in early Martian sediments. Furthermore, this mechanism could explain 13C enrichment of early Martian CO2 without requiring long-term carbon escape into space. A mass balance model calculation using our estimated isotopic fractionation factor indicates the conversion of approximately 20% of volcanic CO2 emissions on early Mars into organics via CO, consistent with the available data for carbon isotopes of carbonate. Although alternative pathways for organic compound production have been proposed, our findings suggest that considerable amounts of organic matter may have been synthesized from CO in a reducing early Martian atmosphere and deposited in sediments.

Zircon Zr[sbnd]Hf isotope disequilibrium during crustal anatexis: A record from the Mesozoic migmatite in the eastern Gangdese arc, South Tibet

Stable zirconium (Zr) isotopes have become the focus of attention as potential tracers of magma crystallization and differentiation processes. However, the effects of partial melting, especially disequilibrium melting, on Zr isotope fractionation remain unclear. Here we report in-situ zircon UPb ages, major and trace elements, and ZrHf isotope data for the migmatites in the eastern Gangdese arc, South Tibet. The leucosomes from the metatexite and diatexite migmatites are generally concordant with the foliation of the paleosome and display diffuse and gradational contacts with the melanosomes, indicating that they are in-source leucosomes. Zircon in the paleosome, the protolith of the migmatites, have UPb age of 361 ± 2 Ma and low 176Hf/177Hf ratios of 0.282399–0.282482. They exhibit intragrain variation in δ94/90Zr values, increasing from the core (−0.10 ‰ to +0.36 ‰) to the rim (+0.14 ‰ to +0.55 ‰) domains. The negative correlation between δ94/90Zr values and Zr/Hf ratios suggests preferential incorporation of light Zr isotopes during the crystallization of the zircon in the protolith. Most zircon in the leucosomes from the metatexite and diatexite migmatites exhibit distinct overgrowth rims around the inherited cores. The inherited cores have consistent UPb ages (ca. 360 Ma), trace elements, and Hf isotopic compositions (0.282362–0.282449) with zircon in the paleosome, indicating in situ partial melting. The inherited cores display δ94/90Zr values ranging from −0.12 ‰ to +0.31 ‰, consistent with the zircon core domains in the paleosome. The overgrowth rims have UPb ages of ca. 102 Ma and display higher 176Hf/177Hf ratios (0.282592–0.282900) and δ94/90Zr values (+0.01 ‰ to +0.63 ‰) than their inherited cores. The elevated 176Hf/177Hf for the overgrowth rims resulted from the retention of unradiogenic 177Hf in the residue due to limited zircon dissolution and more release of radiogenic 176Hf to the melts because of the garnet breakdown, indicating disequilibrium melting. The elevation of δ94/90Zr for the overgrowth rims relative to the inherited cores was not caused by the disequilibrium melting of other Zr-bearing minerals but was mainly controlled by the Zr isotopic composition and dissolution degree of the zircon in the protolith. The preferential melting of isotopically heavy zircon rims would elevate the δ94/90Zr values in the melts relative to their zircon-bearing protoliths. Crustal anatexis may be another important mechanism contributing to the Zr isotope fractionation during crustal differentiation.

Synergies of chemodenitrification and denitrification in a saline inland lake

The interconnection between biotic and abiotic pathways involving the nitrogen and iron biogeochemical cycles has recently gained interest. While lacustrine ecosystems are considered prone to the biotic nitrate reduction (denitrification), their potential for promoting the abiotic nitrite reduction (chemodenitrification) remains unclear. In the present study, batch incubations were performed to assess the potential for chemodenitrification and denitrification in the saline inland lake Gallocanta. Sulfidic conditions are found in top sediments of the system while below (5–9 cm), it presents low organic carbon and high sulfate and ferrous iron availability. Anoxic incubations of sediment (5–9 cm) and water from the lake with nitrite revealed potential for chemodenitrification, especially when external ferrous iron was added. The obtained isotopic fractionation values for nitrite (ɛ15NNO2) were −6.8 and −12.3 ‰ and therefore, fell in the range of those previously reported for the nitrite reduction. The more pronounced ɛ15NNO2 (−12.3 ‰) measured in the experiment containing additional ferrous iron was attributed to a higher contribution of the chemodenitrification over biotic denitrification. Incubations containing nitrate also confirmed the potential for denitrification under autotrophic conditions (low organic carbon, high ferrous iron). Higher reaction rate constants were found in the experiment containing 100 μM compared to 400 μM nitrate. The obtained ɛ15NNO3 values (−8.5 and −15.1 ‰) during nitrate consumption fell in the range of those expected for the denitrification. A more pronounced ɛ15NNO3 (−15.1 ‰) was determined in the experiment presenting a lower reaction rate constant (400 μM nitrate). Therefore, in Gallocanta lake, nitrite generated during nitrate reduction can be further reduced by both the abiotic and biotic pathways. These findings establish the significance of chemodenitrification in lacustrine systems and support further exploration in aquatic environments with different levels of C, N, S, and Fe. This might be especially useful in predicting nitrous oxide emissions in natural ecosystems.

Novel extraction methods and compound-specific isotope analysis of methoxychlor in environmental water and aquifer slurry samples

Multi-element compound-specific stable isotope analysis (ME-CSIA) allows monitoring the environmental behavior and transformation of most common and persistent contaminants. Recent advancements in analytical techniques have extended the applicability of ME-CSIA to organic micropollutants, including pesticides. Nevertheless, the application of this methodology remains unexplored concerning harmful insecticides such as methoxychlor, a polar organochlorine pesticide usually detected in soil and groundwater. This study introduces methods for dual carbon and chlorine compound-specific stable isotope analysis (δ13C-CSIA and δ37Cl-CSIA) of both methoxychlor and its metabolite, methoxychlor olefin, with a sensitivity down to 10 and 100 mg/L, and a precision lower than 0.3 and 0.5 ‰ for carbon and chlorine CSIA, respectively. Additionally, three extraction and preconcentration techniques suitable for ME-CSIA of the target pesticides at environmentally relevant concentrations were also developed. Solid-phase extraction (SPE) and liquid-solid extraction (LSE) effectively extracted methoxychlor (107 ± 27 % and 87 ± 13 %, respectively) and its metabolite (91 ± 27 % and 106 ± 14 %, respectively) from water and aquifer slurry samples, respectively, with high accuracy (Δδ13C and Δδ37Cl ≤ ± 1 ‰). Combining CSIA with polar organic chemical integrative samplers (POCISs) for the extraction of methoxychlor and methoxychlor olefin from water samples resulted in insignificant fractionation for POCIS-CSIA (Δδ13C ≤ ± 1 ‰). A relevant sorption of methoxychlor was detected within the polyethersulfones membranes of the POCISs resulting in temporary carbon isotope fractionation depending on the sorbed mass fraction during the first deployment days. This highlights the critical role of the interactions of polar analytes with POCIS sorbents and membranes in the performance of this method. Altogether, this study proposes a proof of concept for ME-CSIA of methoxychlor and its metabolites, opening the door for future investigations of their sources and transformation processes in contaminated sites.

Insights into fluid evolution and Re enrichment by mineral micro-analysis and fluid inclusion constraints: Evidence from the Maronia Cu-Mo ± Re ± Au porphyry system in NE Greece

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

Energy flux couples sulfur isotope fractionation to proteomic and metabolite profiles in Desulfovibrio vulgaris.

Microbial sulfate reduction is central to the global carbon cycle and the redox evolution of Earth's surface. Tracking the activity of sulfate reducing microorganisms over space and time relies on a nuanced understanding of stable sulfur isotope fractionation in the context of the biochemical machinery of the metabolism. Here, we link the magnitude of stable sulfur isotopic fractionation to proteomic and metabolite profiles under different cellular energetic regimes. When energy availability is limited, cell-specific sulfate respiration rates and net sulfur isotope fractionation inversely covary. Beyond net S isotope fractionation values, we also quantified shifts in protein expression, abundances and isotopic composition of intracellular S metabolites, and lipid structures and lipid/water H isotope fractionation values. These coupled approaches reveal which protein abundances shift directly as a function of energy flux, those that vary minimally, and those that may vary independent of energy flux and likely do not contribute to shifts in S-isotope fractionation. By coupling the bulk S-isotope observations with quantitative proteomics, we provide novel constraints for metabolic isotope models. Together, these results lay the foundation for more predictive metabolic fractionation models, alongside interpretations of environmental sulfur and sulfate reducer lipid-H isotope data.

Compound-specific, intra-molecular, and clumped 13C fractionations in the thermal generation and decomposition of ethane and propane: A DFT and kinetic investigation

The distribution of stable isotopes in organic compounds within geochemical systems reflects the reactions they undergo, which are often kinetically governed and can be elucidated through quantification based on first principles: employing quantum chemical simulations to derive energy barriers and kinetic isotope effects (KIEs), followed by kinetic calculations using these parameters. In this paper, the distribution of 13C in hydrocarbon gases during the thermal generation and decomposition of ethane and propane has been addressed. The work is based on abundant and systematic isotopic data, including the compound- and position-specific 13C compositions, recent improvements in kinetic networks in hydrocarbon generation, and state-of-the-art quantum chemical methods that can process organic geochemical systems involving solid phases. Density Functional Theory computations validate the carbonium path of hydrocarbon generation and the free-radical path of their decomposition under geological conditions. The first step of each path (alkyl sidechain protonation for generation and hydrogen abstraction for decomposition) is the rate-limiting step and determines the 13C fractionations of gaseous hydrocarbons, with the reaction rate constrained by the concentration or accessibility of the active species (hydrated protons and surface free radicals in the two paths, respectively). Alkyl protonation has normal 13C KIEs, but hydrogen abstraction on the surfaces of solid organic matter has inverse ones (substituting 12C by 13C accelerates the reaction). These inverse KIEs explain three isotopic phenomena in gaseous hydrocarbons in their late thermal evolution: 1) the depletion of 13C in ethane and propane accompanied by their decreased fraction in hydrocarbon gases (isotope “rollover”); 2) the reversed 13C sequence with carbon number (δ13Cmethane > δ13Cethane > δ13Cpropane); and 3) the depletion of 13C in the center carbon atoms of residual propane. Isotopic fractionation between gaseous hydrocarbons upon generation is evaluated using the Successive Random Chain-Scission model. The covariation of δ13C in alkanes shows a depletion in CH4 compared with the values expected from the reciprocal of the carbon numbers, indicating that this deviation may be intrinsic instead of mixing with microbial methane. The comparison of intramolecular 13C fractionation of propane between computational and observed data suggests the contribution of isoprenoids at the beginning of the generation, in addition to isotopic homogenization between the center and end carbon atoms through the ring closure of intermediate cations. The 13C–13C clumping exhibits a weak KIE in both the generation and decomposition of ethane; the clumping is essentially stochastically governed. This work demonstrates how first-principle calculations can provide significant insights into the details of geochemical reactions governing the isotopic distributions.