Mean δ18O Research Articles

Spatially-Resolved Integrated Precipitation-Surface-Groundwater Water Isotope Mapping From Crowd Sourcing: Toward Understanding Water Cycling Across a Post-glacial Landscape

Isotopic analyses of δ18O and δ2H of water in the context of the hydrologic cycle have allowed hydrologists to better understand the portioning of water between the different water domains. Isoscapes on a large spatial scale have been created to show isotopic variation in waters as a function of elevation, temperature, distance to coast, and water vapor source. We present the spatial and temporal isotopic results of precipitation, surface water, and groundwater of an ongoing study across Massachusetts, USA in order to establish an isotopic baseline for the region. This represents one of the most comprehensive and detailed isotopic studies of water across a 10,000 sq mi area that has exhaustively sampled important components of the terrestrial hydrologic cycle (precipitation, groundwater, and surface waters). We leverage the support of volunteers and citizen scientists to crowd source samples for isotopic analysis. The database consists of water samples from 14 precipitation sites, 409 ground water sites and 516 surface water sites across the state of Massachusetts, USA. The results indicate that groundwater isotopic composition ranges from δ18O −11 to −4‰ surface water ranges from δ18O −13 to −3.84‰ and precipitation ranges from δ18O −17.88 to −2.89‰. On a first order, the small bias of mean groundwater (−8.7‰) and surface water (−8.0‰) isotopes compared to precipitation δ18O (−7.6‰) supports that groundwater recharge and surface water storage effects through the hydrologic year impact the isotopic composition of surface and groundwater. While differences are distinct, they are larger than previously reported values, but still suggest more importance of summer precipitation than previously acknowledged. On average seasonal amplitudes of precipitation (2.7‰), surface water (1.13‰), and groundwater (~0‰) of the region demonstrate young water fractions of surface water to be 40% with groundwater ~0%. Results demonstrate that mean δ18O in precipitation, surface water and groundwaters are more enriched in heavy isotopes in areas near the coast, than the interior and western portion of Massachusetts. The hope is for this dataset to become an important tool for water management and water resource assessment across the region.

Stable isotopes verify geographical origin of Tibetan chicken

Due to the particularity of origin area, the yield and price of Tibetan chicken are different from those in the plain areas, which leads to chickens from the plains being disguised as Tibetan chickens. In present study, Tibetan chicken and chicken from other four provinces in plain areas were distinguished by stable isotopes and chemometric methods. The cross-validation rate was 97.6%. Secondly, correlation between mean δ13C, δ15N, δ2H and δ18O values in chicken samples and environmentalparameters was investigated. These indicators are closely related to geographical environment. δ13C and δ15N values were positively correlated with longitude (R = 0.955) and altitude (R = 0.796), respectively. δ18O and δ2H values were negatively correlated with latitude (R = 0.903) and altitude (R = 0.938), respectively. At last, we used stable isotopes to trace Tibetan chicken from the different area of Tibet. When four stable isotope ratios were combined, we can distinguish them.

Snow-Pit Record from a Coastal Antarctic Site and Its Preservation of Meteorological Features

AbstractPolar snow pits or ice cores preserve valuable information derived from the atmosphere on past climate and environment changes. A 1.57-m snow-pit record from the coastal site (Styx Glacier) in eastern Antarctica covering the period from January 2011 to January 2015 was discussed and compared with meteorological variables. The dominant contribution of the deposition of sea-salt aerosols due to the proximity of the site to the ocean and processes of sea ice formation was revealed in the ionic concentrations. Consistent seasonal peaks in δ18O, δD, MSA, , and indicate the strong enhancement of their source during warm periods, whereas the sea-salt ions (Na+, K+, Mg2+, Ca2+, Cl−, and ) exhibit a distinct distribution. Monthly mean δ18O positively correlates with the air temperature record from an automatic weather station (AWS) located in the main wind direction. Despite the shortness of the record, we suspect that the slight depletion of the isotopic composition and lowering of the snow accumulation could be related to the cooler air temperature with the decrease of open sea area. Consistency with previous studies and the positive correlation of sea-salt ions in the snow pit indicate the relatively good preservation of snow layers with noticeable climate and environmental signals [e.g., changes in sea ice extent (SIE) or sea surface temperature]. We report a new snow-pit record, which would be comparative and supportive to understand similar signals preserved in deeper ice cores in this location.

The dendroclimatic value of oak stable isotopes

Tree-ring stable oxygen and carbon isotope ratios (δ18O and δ13C) are an important archive for climate reconstructions. However, it remains unclear whether the polyvinyl acetate emulsion, often used for the preservation and fixation of wood samples, influences δ18O and δ13C signals. Further uncertainties are associated with the possible effects of geographical origin and cambial age of historical samples. Here, we present annually-resolved and absolutely-dated δ18O and δ13C measurements of 21 living oaks (Quercus robur and Q. petraea) from the Czech Republic. We find that the δ18O and δ13C signals in the extracted alpha-cellulose are not affected by polyvinyl acetate treatment. Covering the entire 20th century and reaching until 2018 CE, our dataset reveals spatial and temporal coherency within and between the individual δ18O and δ13C chronologies of different oak species, sample locations, and tree ages. Highly significant (p < 0.01) Pearson’s correlation coefficients of the site-specific δ13C and δ18O chronologies range from 0.48–0.77 and 0.36–0.56, respectively. The isotopic inter-series correlations of Q. robur and Q. petraea from the same site are 0.75 and 0.43 for the mean δ13C and δ18O values, respectively. Significant (p < 0.01) correlations of 0.49 and 0.84 are found for δ13C and δ18O, respectively, when all measurements from all sampling locations and tree ages are included. Our study shows that non-pooled oak δ18O and δ13C measurements from both species, different locations, and diverse tree ages can be combined into robust isotopic chronologies for climate reconstructions.

Origin of Middle-Upper Cambrian dolomites in eastern Laurentia: A case study from Belle Isle strait, western Newfoundland

The Middle and Upper Cambrian Port au Port Group of western Newfoundland consists mainly of mixed carbonates and siliciclastics and is composed of the March Point, Petit Jardin, and Berry Head formations. Samples were collected from the core NF-02 that spans the uppermost Hawke Bay (40 m), the March Point (~83 m thick) and the lowermost Petit Jardin (~47 m). Petrographic examination of carbonates of the March Point and Petit Jardin carbonates reveals three generations of dolomite: (i) micritic to near-micritic (D1, 4 μm −35 μm) fabric-retentive dolomite, (ii) coarse crystalline sucrosic (D2, 60 μm−150 μm) fabric-destructive dolomite (sub-to euhedral zoned rhombs with clear rim and cloudy core), and (iii) coarse anhedral (D3, >0.5 mm) fracture-filling saddle dolomite. The microthermometric measurements of primary two-phased fluid inclusions retained in D2, and D3 samples yielded homogenization temperatures (Th) showing a general increase with burial. The mean values of Th and salinity are 89.1 ± 6.4 °C vs 21.2 ± 2.2 eq. wt% NaCl, and 110 ± 8.2 °C vs 21.1 ± 4.7 eq. wt% NaCl, respectively. The investigated dolomites show a decrease of Sr from D1 (102 ± 49 ppm) to D3 (47 ± 15 ppm) which reflects the influence of progressive burial. The mean δ18O values decrease from D1 (−6.3 ± −1.1‰ VPDB), to D3 (−9.7 ± 1.7‰ VPDB) where D2 (−7.6 ± 1.2‰ VPDB) is in the middle. The estimated δ18O values of the D1 parent fluid (−5 to −10‰ VSMOW) are bracketed by those suggested for the Middle Cambrian meteoric and seawaters. The fluid-inclusion gas analyses provided CO2/CH4 and N2/Ar ratios coherent with the conclusions from the petrographic examination and geochemical compositions.

Hydrological system in Quaternary clastic deposits, Mehedinţi County, Romania: isotope composition, chemistry and radiocarbon dating

Abstract A groundwater geochemistry study was carried out on 24 samples collected from different springs and wells situated in a plateau area at an elevation of 200–300 m in the Mehedinţi County, southwestern Romania. The study was motivated by the fact that springs have represented the only source of potable water in the region, only recently completed by tens of metres-deep well drillings. Spring distributions and geological data reveal the presence of a multilayered system situated in the Lower Quaternary deposits. The mean δ 18 O and δ D values of groundwater, −9.8 and −67.8‰, respectively, reflect the yearly weighted mean of the isotopic composition of precipitation, demonstrating locally derived recharge. The Piper ternary diagrams indicate that the dominant hydrochemical type is HCO 3 − –Ca 2+ –Mg 2+ with transition towards higher SO 4 2− and Mg 2+ contents to the deeper aquifer. The anions vary from HCO 3 − with transition to no dominant type and with Cl − contents higher for the shallower aquifer. The sequence of abundance of cations is generally Ca 2+ &gt; Mg 2+ &gt; K + &gt; Na + and for anions: HCO 3 − &gt; SO 4 2− &gt; Cl − &gt; NO 3 − &gt; F − . Radiocarbon dating of dissolved inorganic carbon indicates a subrecent recharge of the aquifers. The vertical and lateral variations in groundwater chemistry may vary, and are influenced by lateral lithologic variation of the Quaternary clastic deposits. This is an unpredictable quality factor when taking the decision for the drinking water drill locations.

Diagenesis of the Vaca Muerta Formation, Neuquén Basin: Evidence from petrography, microthermometry and geochemistry

The Tithonian Vaca Muerta Formation (500 m-thick marine carbonates) in the Pampa de Tril area is a potential unconventional hydrocarbon reservoir but earlier studies rarely focused on its diagenetic history. It constitutes the upper part of the lower Mendoza Group in the Neuquén Basin, western Argentina. Petrographic examinations reveal four generations of calcite (C1, C2, Cb and C3). The microbial lime mudstone (C1, <4 μm), which exhibits dull cathodoluminescence (CL), is the most abundant with mean δ18O value of −7.2 ± 1.3‰ (VPDB) and δ13C of −1 ± 3.3‰ (VPDB) and deemed to have deposited in tropical warm shallow-water settings. The equant calcite cement (C2, 25 μm–140 μm) exhibits red CL and is associated with recrystallization of bioclasts and micritic matrix. The fibrous calcite (Cb, 35 μm–125 μm) fills parallel-to-bedding antitaxial veins (beefs) and shows bright orange CL. Its δ18O and δ13C values are more depleted (−10.7 ± 2.2‰ VPDB and −4.8 ± 3.9‰ VPDB, respectively) relative to those of C1, which is consistent with the occurrence of hydrocarbon fluid inclusions and may imply precipitation during a mid-to late stage of diagenesis within the oil window. The fracture-filling C3 consists of coarse subhedral crystals (40 μm–5 mm) showing bright orange CL, which has been interpreted as precipitated during deep burial conditions at temperatures around 118 ± 26.8 °C based on fluid-inclusion microthermometry. The relative depletion of Fe and Mn from C1 to C3 and the low concentration of U, may imply a relatively closed system of low water/rock interaction and restricted meteoric alteration. The shale normalized (REESN) patterns of C1, Cb and C3 generally exhibit parallel patterns with a distinct positive Eu anomaly and progressive enrichment towards the MREE and HREE. The positive Eu (Eu/Eu*)SN anomalies reflect the impact of dissolution of plagioclase feldspars by circulation of the diagenetic fluids through the surrounding siliciclastics in the basin.The Ce (Ce/Ce*)SN and La (La/La*)SN anomalies of Cb and C3 are consistent with precipitation under reducing conditions of deep burial settings. The Vaca Muerta carbonates are enriched in organic matter (up to 12%) that fills the pores but permeability is insignificant.

Alpine Holocene tree-ring dataset: age-related trends in the stable isotopes of cellulose show species-specific patterns

Abstract. Stable isotopes in tree-ring cellulose are important tools for climatic reconstructions even though their interpretation could be challenging due to nonclimate signals, primarily those related to tree aging. Previous studies on the presence of tree-age-related trends during juvenile as well as adult growth phases in δD, δ18O, and δ13C time series yielded variable results that are not coherent among different plant species. We analyzed possible trends in the extracted cellulose of tree rings of 85 larch trees and 119 cembran pine trees, i.e., in samples of one deciduous and one evergreen conifer species collected at the tree line in the Alps, covering nearly the whole Holocene. The age trend analyses of all tree-ring variables were conducted on the basis of mean curves established by averaging the cambial-age-aligned tree series. For cambial ages over 100 years, our results prove the absence of any age-related effect in the δD, δ18O, and δ13C time series for both the evergreen and the deciduous conifer species, with the only exception being larch δD. However, for lower cambial ages, we found trends that differ for each isotope and species; i.e., mean δ13C values in larch do not vary with aging and can be used without detrending, whereas those in cembran pine show a juvenile effect, and the data should be detrended. Mean δ18O values present two distinct aging phases for both species, complicating detrending. Similarly, mean δD values in larch change in the first 50 years, whereas cembran pine changes between 50 and 100 years. Values for these two periods of cambial age for δD and δ18O should be used with caution for climatic reconstructions, ideally complemented by additional information regarding mechanisms for these trends.

Oxygen-Hafnium-Neodymium Isotope Constraints on the Origin of the Talnakh Ultramafic-Mafic Intrusion (Norilsk Province, Russia)

Abstract The ultramafic-mafic Talnakh intrusion in the Norilsk province (Russia) hosts one of the world’s major platinum group element (PGE)-Cu-Ni sulfide deposits. This study employed a multitechnique approach, including in situ Hf-O isotope analyses of zircon combined with whole-rock Nd isotope data, in order to gain new insights into genesis of the Talnakh economic intrusion. Zircons from gabbrodiorite, gabbroic rocks of the layered series, and ultramafic rocks have similar mantle-like mean δ18O values (5.39 ± 0.49‰, n = 27; 5.64 ± 0.48‰, n = 34; and 5.28 ± 0.34‰, n = 7, respectively), consistent with a mantle-derived origin for the primary magma(s) parental to the Talnakh intrusion. In contrast, a sulfide-bearing taxitic-textured troctolite from the basal part of intrusion has high δ18O (mean of 6.50‰, n = 3), indicating the possible involvement of a crustal component during the formation of sulfide-bearing taxitic-textured rocks. The Hf isotope compositions of zircon from different rocks of the Talnakh intrusion show significant variations, with ɛHf(t) values ranging from –3.2 to 9.8 for gabbrodiorite, from –4.3 to 11.6 for unmineralized layered-sequence gabbroic rocks, from 2.3 to 12 for mineralized ultramafic rocks, and from –3.5 to 8.8 for mineralized taxitic-textured rocks at the base of the intrusion. The significant range in the initial 176Hf/177Hf values is ascribed to interaction of distinct magma sources during formation of the Talnakh intrusion. These include (1) a juvenile source equivalent to the depleted mantle, (2) a subcontinental lithospheric source, and (3) a minor crustal component. Initial whole-rock Nd isotope compositions of the mineralized taxitic-textured rocks from the base of the intrusion (mean ɛNd(t) = –1.5 ± 1.8) differ from the other rocks, which have relatively restricted ranges in initial ɛNd (mean ɛNd = 0.9 ± 0.2). The major set of ɛNd values around 1.0 at Talnakh is attributed to limited crustal contamination, presumably in deep magma chambers, whereas the smaller set of negative ɛNd values in taxitic-textured rocks is consistent with greater involvement of a crustal component and reflects an interaction with the wall rocks during emplacement.

Isotope Composition of Precipitation, Groundwater, and Surface and Lake Waters from the Plitvice Lakes, Croatia

The application of tritium, 2H, and 18O in the characterization of the precipitation, groundwater, and surface and lake water of the Plitvice Lakes (PL), Croatia, over the 1979–2019 period is presented. An increase in the mean annual air temperature of 0.06 °C/year and in the annual precipitation amount of 10 mm/year is observed. The good correlation of the tritium activity concentration in the PL and Zagreb precipitation implies that the tritium data for Zagreb are applicable for the study of the PL area. The best local meteoric water line at PL was obtained by the reduced major axis regression (RMA) and precipitation-weighted ordinary least squares regression (PWLSR) approaches: δ2HPWLSR = (7.97 ± 0.12) δ18O + (13.8 ± 1.3). The higher deuterium excess at PL (14.0 ± 2.2 ‰) than that at Zagreb reflects the higher altitude and influence of the Mediterranean precipitation. The δ2H in precipitation ranges from −132.4‰ to −22.3‰ and δ18O from −18.3 ‰ to −4.1‰. The much narrower ranges in the groundwater (&lt;1‰ in δ18O, &lt;10‰ in δ2H) indicate the good mixing of waters in aquifers and short mean residence times. The higher average δ2H in all three karst springs observed after 2003 can be attributed to the increase in the mean air temperature. The mean δ2H and δ18O values in the surface and lake water increase downstream due to the evaporation of surface waters. There is no significant difference between the surface water line and the lake water line (2011–2014). The stable isotope composition of the surface and lake waters reacts to extreme hydrological conditions.

Chronological characteristics for snow accumulation on Styx Glacier in northern Victoria Land, Antarctica

AbstractUnder the potential to reconstruct the past climatic and atmospheric conditions from a deep ice core in the coastal Antarctic site (Styx Glacier), an 8.84 m long firn core (73°50.975′ S, 163°41.640′ E; 1623 m a.s.l.) was initially studied to propose a reliable age scale for the local estimation of snow accumulation rate. The seasonal variations of δ18O, methanesulfonic acid (MSA) and non-sea-salt sulfate (nssSO42–) were used for the firn core dating and revealed 25 annual peaks (from 1990 to 2014) with volcanic sulfate signal. The observed declining trend in annual accumulation rate with a mean value of 146 ± 60 kg m–2a–1is likely to be linked to the changes of sea-ice extent in the Ross Sea region. Moreover, the temporal variation of the annual mean δ18O, an annual flux of MSA and nssSO42–also likely to be under the influence of ice-covered and open water area. This study suggests a potential to recover past changes in an oceanic environment and will be useful for the interpretation of the long ice core drilled at the same site.

KV01 zircon—A potential New Archean reference material for microbeam U-Pb age and Hf-O isotope determinations

To meet the rapid development of zircon U-Pb geochronology and Hf-O isotope geochemistry, it is imperative to develop well-characterized zircon reference materials for microbeam analysis. Here, zircon KV01 separated from the Kaap Valley pluton, South Africa is introduced as a potential Archean reference material for microbeam U-Pb age and Hf-O isotope determination. SIMS and LA-ICP-MS U-Pb isotopic measurements gave grand mean 207Pb/206Pb ages of 3233±16 Ma (2s, n=90) and 3230±26 Ma (2s, n=52), which are consistent with reported CA-ID-TIMS results. Slight heterogeneity of oxygen isotopes is revealed by SIMS analyses that yielded a relatively large δ18O range of 4.61–6.51‰. Among them, the zircon grains with clear oscillatory zones give a grand mean δ18O value of 6.17±0.33‰ (2s), which is suggested to record the primary O isotopic compositions. The homogeneity in the Hf isotopic compositions of KV01 zircon was checked by the laser ablation and solution MC-ICP-MS methods. They yielded consistent results with a recommended 176Hf/177Hf ratio of 0.280810±0.000013 (2s). The results reported here demonstrate that KV01 zircon could be a reliable reference material for microbeam 207Pb/206Pb age and Hf isotope determinations of ancient zircons, and be suitable as a quality monitor for SIMS oxygen isotopic analysis.

Paleoclimatic investigations using isotopic signatures of the Late Pleistocene-Holocene groundwater of the stratified aquifers in Kuwait

The study attempts to determine paleo recharge sources for two major aquifer units of Kuwait, namely, Kuwait Group Aquifer (KGA), and Dammam Formation (DFm) were collected and analyzed for major ions and isotopes. The obtained results of 14C ages indicated that the groundwater samples ranged from 31.9 Ky to 3.9 Ky in DFm and 23.3 Ky to 0.8 Ky in KGA. The variations in δ18O signatures with respect to age reflected that there were two major sources of rainwater such as enriched southern Indian Ocean monsoon and the depleted northwesterly (Mediterranean) vapor source. The samples found to show variations during the three marine isotopic stages (MIS 1–3), Heinrich events, Bolling-Allerod, and Dryas time periods in both aquifers. A shift in the Intertropical convergence zone (ITCZ) was witnessed in the groundwater of both aquifers from 7.8 Ky to 4.9 Ky. The variation in the Holocene climate is mainly due to the influence of tropospheric easterly jet governed by the swing in ITCZ , as a result of Holocene volcanism. The mean δ18O values of DFm samples (-3.81‰) reflect depletion than KGA samples (-2.31‰), and the d-excess values were −0.95‰ and 2.05‰ respectively. Thus it could be inferred that the DFm was predominantly recharged during Late Pleistocene period and it was in a relatively cooler climate than recharge environment of KGA. The study infers that KGA was recharged between 26oN and 26.8oN latitudes, and that of the DFm was noted to be recharged (south west of Kuwait) in two different patches between 25.8oN and 26.2oN and 26.7oN-27.4oN latitudes during Late Pleistocene. The KGA was concluded to be recharged between 25.5oN and 27.5oN latitudes, south of Kuwait, during Holocene.

Early and pervasive dolomitization by near‐normal marine fluids: New lessons from an Eocene evaporative setting in Qatar

AbstractThe upper Palaeocene–lower Eocene Umm er Radhuma Formation in the subsurface of Qatar is dominated by subtidal carbonate depositional packages overlain by bedded evaporites. In Saudi Arabia and Kuwait, peritidal carbonate depositional sequences with intercalated evaporites and carbonates in Umm er Radhuma have been previously interpreted to have been dolomitized via downward reflux of hypersaline brines. Here, textural, mineralogical and geochemical data from three research cores in Qatar are presented which, in contrast, are more consistent with dolomitization by near‐normal marine fluids. Petrographic relationships support a paragenetic sequence whereby dolomitization occurred prior to the formation of all other diagenetic mineral phases, including chert, pyrite, palygorskite, gypsum, calcite and chalcedony, which suggests that dolomitization occurred very early. The dolomites occur as finely crystalline mimetic dolomites, relatively coarse planar‐e dolomites, and coarser nonplanar dolomites, all of which are near‐stoichiometric (50.3 mol% MgCO3) and well‐ordered (0.73). The dolomite stable isotope values (range −2.5‰ to +1‰; mean δ18O = −0.52‰) and trace element concentrations (Sr = 40 to 150 ppm and Na = 100 to 600 ppm) are compatible with dolomitization by near‐normal seawater or mesohaline fluids. Comparisons between δ18O values from Umm er Radhuma dolomite and the overlying Rus Formation gypsum further suggest that dolomitization did not occur in fluids related to Rus evaporites. This study provides an example of early dolomitization of evaporite‐related carbonates by near‐normal seawater rather than by refluxing hypersaline brines from overlying bedded evaporites. Further, it adds to recent work suggesting that dolomitization by near‐normal marine fluids in evaporite‐associated settings may be more widespread than previously recognized.

Generation of Eoarchean continental crust from altered mafic rocks derived from a chondritic mantle: The ∼3.72 Ga Aktash gneisses, Tarim Craton (NW China)

Our understanding of crust – mantle evolution and geodynamics of the early Earth has been hampered by the scarcity of Hadean to Eoarchean rocks and by the almost ubiquitous isotopic disturbance of the oldest rocks. Here we present in-situ zircon U-Pb ages, O-OH and Lu-Hf isotopes, as well as whole-rock Sr-Nd-Hf-Pb isotopes for the recently identified Eoarchean Aktash gneisses in the Tarim Craton, NW China. The new age data confirm that the Aktash gneisses were formed at least by ∼3.72 Ga and were affected by two metamorphic events at ∼3.56 and ∼2.0 Ga, respectively. Whole-rock isotopic data show that the Sr-Nd-Hf-Pb isotopic systematics have all been variously disturbed by ∼2.0 Ga regional granulite facies metamorphism, resulting in decoupling of Nd-Hf isotopic systematics that is, in some samples, similar to that observed in SW Greenland. The least disturbed sample (16ALT67), however, yielded chondritic to slightly sub-chondritic whole-rock εNd (−0.3) and εHf (−0.9). This is consistent with the in-situ magmatic zircon εHf (weighted mean −0.2 to −1.8) for most samples of the Aktash gneisses, suggesting a mafic source derived from chondritic mantle with a short crustal residence time. Our data thus provide no evidence for the presence of an Eoarchean depleted mantle or a Hadean enriched crust, implying that early Earth crust – mantle differentiation was either limited or balanced by large-scale crustal recycling. In-situ zircon O–OH data show that metamorphism and later alteration tend to decrease the zircon δ18O of the Aktash gneisses, and the weighed mean δ18O of pristine magmatic zircons (6.2–6.3‰) from the least disturbed samples indicate that the mafic source was mildly altered at low temperature by the early hydrosphere, facilitating partial melting and formation of some of the earliest preserved continental crust known on Earth.

Water Sources and Factors Controlling Hydro-chemical Compositions in the Yiluo River Basin

An important tributary in the middle stream of the Yellow River, the Yiluo River consists of the Luohe River and Yihe River, which converge at Yanshi City. Mining activities were widely distributed in the upstream of the Yiluo River Basin (YRB), while residential areas concentrated in the downstream were coupled with extensively industrial and agricultural activities. To illustrate the influences of variable anthropogenic activities on the hydro-chemical composition of river water of the YRB, water samples from the main stream and tributaries were collected in the flood season (August) and normal season (December), respectively. The hydrogen and oxygen isotope values coupled with cation and anion content were analyzed. Temporal and spatial variations of hydrogen and oxygen isotopes and ion content were utilized to elucidate the sources and factors controlling the hydro-chemical composition of the river water, and to illustrate the pathways of human effects. The results demonstrated that:① Average hydrogen and oxygen isotope values (δD and δ18O) of Luo River water were -56‰ and -7.9‰, and -55‰ and -8.1‰ in the flood season and normal season, respectively. Mean δD and δ18O values of Yi River water were -49‰ and -6.9‰, and -53‰ and -7.8‰ in the flood season and normal season, respectively. These temporal variations indicated that river water was mainly recharged by local atmospheric precipitation. ② The dominant water hydro-chemical type was HCO3-SO4-Ca-Mg in the main stream of the YRB, and the ratios of Ca2+ and HCO3- molar equivalent concentrations in the flood season were lower than those in the normal season, while the ratios of SO42- molar equivalent concentrations were higher than those in the normal season, indicating more sulfate dissolved in the river water in the flood season. ③ Carbonic acid and sulfuric acid simultaneously reacted with carbonate and silicate rocks, and in the Luo River more carbonate rocks were weathered, while in the Yi River more silicate rocks were weathered. ④ Human effects on river water were mainly concentrated in the upstream where wastewater input was derived from mining activities, while in the downstream pollution of the river was due to industrial wastewater and sewage input. ⑤ Spatial variations of sulfate sulfur isotope values were mostly due to differences between anthropogenic activities in the upstream and downstream of the Yiluo River. Negative sulfur isotope values in the upstream river water confirmed dissolved sulfate from sulfide mineral oxidation, which also indirectly verified the rock chemical weathering by sulfuric acid in this area. Positive sulfur isotope values in downstream river water were connected with industrial wastewater and sewage.

An entropy-based analysis method of precipitation isotopes revealing main moisture transport corridors globally

Abstract The hydrogen (δD) and oxygen (δ18O) isotopic compositions in the water molecule have been widely used as tracers for studying the global water cycle. In 1961, the Global Network of Isotopes in Precipitation (GNIP) was established to measure D and 18O isotopes contents in precipitation around the world. However, on the spatial scale, the long-term arithmetic and/or long-term precipitation weighted mean δD and δ18O have been most commonly used to interpret the GNIP isotope data for over sixty years. The spatial distributions of mean δD and δ18O depict well the regional moisture transport, but they vary predominantly with latitude on the global scale, especially over continental areas, obscuring the continental and circulation effects. We developed a new method of using the entropy concept to reanalyze precipitation isotopic compositions data from GNIP. Calculated entropies of isotopic compositions in precipitation at GNIP stations around the world strongly correlate in a linear fashion with a slope coefficient close to unity. The spatial distributions of both isotopic compositions entropies generally reveal oceanic sources of water vapor and main moisture transport pathways from oceans to continents globally, with different patterns between summer and winter seasons. Although these results have mostly been reported in previous studies, they provide the verification of this new analysis method. The entropy method proposed here is expected to provide a new tool for data interpretation of water isotopic compositions, with implications for tracing global hydrological processes.

Long-Term Isotope Records of Precipitation in Zagreb, Croatia

The isotope composition of precipitation has been monitored in monthly precipitation at Zagreb, Croatia, since 1976. Here, we present a statistical analysis of available long-term isotope data (3H activity concentration, δ2H, δ18O, and deuterium excess) and compare them to basic meteorological data. The aim was to see whether isotope composition reflected observed climate changes in Zagreb: a significant increase in the annual air temperature and larger variations in the precipitation amount. Annual mean δ18O and δ2H values showed an increase of 0.017‰ and 0.14‰ per year, respectively, with larger differences in monthly mean values in the first half of the year than in the second half. Mean annual d-excess remained constant over the whole long-term period, with a tendency for monthly mean d-excess values to decrease in the first half of the year and increase in the second half due to the influence of air masses originating from the eastern Mediterranean. Changes in the stable isotope composition of precipitation thus resembled changes in the temperature, the circulation pattern of air masses, and the precipitation regime. A local meteoric water line was obtained using different regression methods, which did not result in significant differences between nonweighted and precipitation-weighted slope and intercept values. Deviations from the Global Meteoric Water Line GMWL (lower slopes and intercepts) were observed in two recent periods and could be explained by changes in climate parameters. The temperature gradient of δ18O was 0.33‰/°C. The tritium activity concentrations in precipitation showed slight decreases during the last two decades, and the mean A in the most recent period, 2012–2018, was 7.6 ± 0.8 Tritium Units (TU).

Can We Detect Changes in Amazon Forest Structure Using Measurements of the Isotopic Composition of Precipitation?

AbstractLarge‐scale (&gt;500 km) spatial gradients of precipitation oxygen isotope ratios (δ18Op) hold information about the hydrological cycle. They result from the interplay between rainout and evapotranspiration along air‐parcel paths, but these counteracting effects are difficult to disentangle, complicating quantification of the effect of land cover change on δ18Op. We show that disentangling can qualitatively be achieved using climate model simulations with a land‐derived precipitation tracer for tropical South America. We then either vary land cover as observed since 1870 or replace Amazon forests with bare land to determine the resulting signals. Our results indicate that effects of historically changing land cover on annual mean δ18O isotope‐ratio gradients are small and unlikely detectable, although there is a noticeable signal during the dry season. Furthermore, the effect of changes in water recycling on Amazon δ18Op in paleo‐records may have been overestimated and need reinterpretation.

Stable Isotope Reveals Tap Water Source under Different Water Supply Modes in the Eastern Margin of the Qinghai–Tibet Plateau

Based on 1260 tap water samples gathered monthly and 136 surface water samples collected seasonally in the eastern margin of the Qinghai–Tibet Plateau, the local tap water line, the basic spatiotemporal characteristics of tap water isotopes, and their indication for water source under different water supply modes were discussed, linking the local tap water supply and water source information. A new tap water isotopes data set based on dense sampling sites was established, which was reliable for the analysis of tap water isotope features, tap water supply management, and tap water sources. The main conclusions are: (1) The local tap water lines in Gannan and Longnan are δ2H = (7.06 ± 0.17) δ18O + (3.24 ± 1.75) (r2 = 0.81, p &lt; 0.01) and δ2H = (5.66 ± 0.09) δ18O + (−8.12 ± 0.82) (r2 = 0.82, p &lt; 0.01), respectively. (2) The annual mean δ2H and δ18O in tap water show an increasing trend from southwest to northeast. The seasonal differences of δ2H and δ18O in tap water in Gannan and Longnan are small. (3) The correlation of tap water isotopes with those in main source water is high, while that of isotopes in tap water with those in non-water source is low. Under the central water supply mode by local tap water company, tap water isotopes in Gannan where groundwater is the direct water source show weak connection with those in surface water and precipitation, and those in tap water in Longnan with surface water as main source water reveal good connection with isotopes in surface water. Under mixed water supply modes, tap water isotopes indicate that surface water is the main tap water source in Gannan and Longnan with multiple water sources.