Changes In Isotopic Composition Research Articles

Zinc- and cadmium-isotope evidence for redox-driven perturbations to global micronutrient cycles during Oceanic Anoxic Event 2 (Late Cretaceous)

This study uses organic-rich sediments from the Tarfaya Basin, Morocco, to assess the Cd- and Zn-isotope response to dramatic global palaeoenvironmental change during the Cenomanian–Turonian interval (Late Cretaceous). These organic-rich continental-margin deposits include an expression of Oceanic Anoxic Event 2 (OAE 2, ∼94 Ma), an interval associated with the spread of low-oxygen marine environments and widespread burial of organic-rich sediments. Due to placement of the Tarfaya Basin in a region of upwelling and relatively constant local environmental conditions, the stratigraphic variations in δ114Cd and δ66Zn values largely reflect changes in the seawater isotopic composition of the sub-surface proto-North Atlantic Ocean. Positive shifts of ∼0.2–0.3‰ away from background values in δ114Cd and δ66Zn are observed during the main phase of the positive carbon-isotope excursion associated with OAE 2. These isotopic shifts are coeval with decreases in Cd/TOC and Zn/TOC ratios and thus imply that drawdown of isotopically light Cd and Zn from seawater inventories was a result of extensive burial of these metals in organic-rich marine sediments globally. Low δ66Zn values during the Plenus Cold Event, a cooler episode during OAE 2, are similar in timing and magnitude to variations found in the English Chalk (Eastbourne, UK) and support the inference of a global control on these isotopic excursions. The δ66Zn values during the Plenus Cold Event are taken to record global oxygenation, possibly including the remobilization of isotopically light Zn from continental-margin sediments. A considerably smaller change in δ114Cd values for this interval implies that the Cd- and Zn-isotope systems can provide information about slightly different environmental processes, with global seawater composition with respect to Zn also being influenced by the magnitude of oxic removal sinks and isotopically light Zn input fluxes from sediments and hydrothermal fluids.

Cu isotope ratios are meaningful in ovarian cancer diagnosis

BackgroundOvarian cancer diagnosis is currently based on imaging and circulating CA-125 concentrations with well-known limits to sensitivity and specificity. New biomarkers are required to complement CA-125 testing to increase effectiveness. Increases in sensitivity of isotopic separation via multi collector inductively coupled plasma-mass spectrometry have recently allowed highly accurate measurement of copper (Cu) isotopic variations. Studies in breast cancer patients have revealed changes of serum copper isotopic composition demonstrating the potential for development as a cancer biomarker. Evaluating 65Cu/63Cu ratios (δ65Cu) in serum samples from cancer patients has revealed a strong correlation with cancer development. In this study blood samples from forty-four ovarian cancer patients, and 13 ovarian biopsies were investigated. ResultsHere we demonstrate that changes in Cu isotopes also occurs in ovarian cancer patients. Copper composition determined by multiple collector inductively coupled plasma mass spectrometry revealed that the copper isotopic ratio δ65Cu in the plasma of 44 ovarian cancer patient cohort was significantly lower than in a group of 48 healthy donors, and indicated that serum was enriched for 63Cu. Further analysis revealed that the isotopic composition of tumour biopsies was enriched for 65Cu compared with adjacent healthy ovarian tissues. ConclusionsWe propose that these changes are due to increase lactate and Cu transporter activities in the tumour. These observations demonstrate that, combined with existing strategies, δ65Cu could be developed for use in ovarian cancer early detection.

Shifts in carbon and nitrogen stable isotope composition and epicuticular lipids in leaves reflect early water-stress in vineyards

Changes in leaf carbon and nitrogen isotope composition (δ13C and δ15N values) and the accumulation of epicuticular lipids have been associated with plant responses to water stress. We investigated their potential use as indicators of early plant water deficit in two grapevine (Vitis vinifera L.) cultivars, Chasselas and Pinot noir, that were field-grown under well-watered and water-deficient conditions. We tested the hypothesis that the bulk δ13C and δ15N values and the concentrations of epicuticular fatty acids may change in leaves of similar age with the soil water availability. For this purpose, leaves were sampled at the same position in the canopy at different times (phenological stages) during the 2014 growing season. Bulk dry matter of young leaves from flowering to veraison had higher δ13C values, higher total nitrogen content, and lower δ15N values than old leaves. In both cultivars, δ15N values were strongly correlated with plant water deficiency, demonstrating their integration of the plant water stress response. δ13C values recorded the water deficiency only in those plants that had not received foliar organic fertilization. The soil water deficiency triggered the accumulation of C>26 fatty acids in the cuticular waxes. The compound-specific isotope analysis (CSIA) of fatty acids from old leaves showed an increase in δ13C among the C16-C22 chains, including stress signaling linoleic and linolenic acids. Our results provide evidence for leaf 13C-enrichment, 15N-depletion, and enhanced FA-chain elongation and epicuticular accumulation in the grapevine response to water stress. The leaf δ13C and δ15N values, and the concentration of epicuticular fatty acids can be used as reliable and sensitive indicators of plant water deficit even when the level of water stress is low to moderate. They could also be used, particularly the more cost-efficient δ13C and δ15N measurements, for periodic biogeochemical mapping of the plant water availability at the vineyard and regional scale.

Retrospective Analysis of Tree Decline Based on Intrinsic Water-Use Efficiency in Semi-Arid Areas of North China

Long-term tree growth is significantly affected by climate change, which have become a global concern. Tree-ring width and isotopic information can show how trees respond to climate change on a long-term scale and reveal some phenomena of tree decline or death. In this study, we used isotopic techniques and investigated annual changes in carbon isotope composition and tree-ring width of Populus simonii Carr. in Zhangbei, as well as trends in tree-ring carbon discrimination (Δ13C) and iWUE in normal, mildly declining and severely declining trees, in order to make a retrospective analysis and further understand the process of tree decline. We found that there were significant differences (p < 0.01 **) in δ13C, Δ13C, ci and iWUE at different decline stages, meaning that the δ13C and iWUE could be new indicators of tree health. The iWUE of all groups increased significantly, while the growth rate of declined P. simonii was much higher than that of normal growth P. simonii. According to the analysis, there may be a threshold of iWUE for healthy trees, which once the threshold value is exceeded, it indicates that trees are resistant to adversity and their growth is under stress. Similarly, the changing trend of BAI supports our conclusion with its changes showed that tree growth became slower and slower as degradation progressed. iWUE inferred from tree-ring stable carbon isotope composition is a strong modulator of adaptation capacity in response to environmental stressors under climate change. Elevated annual temperatures and increased groundwater depth are all contributing to the decline of P. simonii in north China.

Large S isotope and trace element fractionations in pyrite of uranium roll front systems result from internally-driven biogeochemical cycle

Complex pyrite textures associated with large changes in isotopic and trace element compositions are routinely assumed to be indicative of multi-faceted processes involving multiple fluid and sulfur sources. We propose that the features of ore-stage pyrite from roll front deposits across the world, revealed in exquisite detail via high-resolution trace element mapping by LA-ICP-MS, reflect the dynamic internal evolution of the biogeochemical processes responsible for sulfate reduction, rather than externally driven changes in fluid or sulfur sources through time. Upon percolation of oxidizing fluids into the reduced host-sandstones, roll front systems become self-organized, with a systematic reset of their activity cycle after each translation stage of the redox interface down dip of the aquifer. Dominantly reducing conditions at the redox interface favor the formation of biogenic framboidal pyrite (δ34S from −30.5 to −12.5‰) by bacterial sulfate reduction and the genesis of the U mineralization. As the oxidation front advances, oxidation of reduced sulfur minerals induces an increased supply of sulfate and metals in solution to the bacterial sulfate reduction zone that has similarly advanced down the flow gradient. Hence, this stage is marked by increased rates of the bacterial sulfate reduction associated with the crystallization of variably As-Co-Ni-Mo-enriched concentric pyrite (up to 10,000′s of ppm total trace contents) with moderately negative δ34S values (from −13.7 to −7.5‰). A final stage of pyrite cement with low trace element contents and heavier δ34S signature (from −6.9 to +18.8‰) marks the end of the roll front activity cycle and the transition from an open to a predominantly closed system behavior (negligible advection of fresh sulfate). Blocky pyrite cement is formed using the remaining sulfate, which now becomes quickly heavy according to a Rayleigh isotope fractionation process. This ends the cycle by depleting the nutrient supplies for the sulfate-reducing bacteria and cementing pore spaces within the host sandstone, effectively restricting fluid infiltration. This internally-driven roll front activity cycle results in systematic, large S isotope and trace element fractionation. Ultimately, the long-time evolution of the basin and fluid sources control the metal endowment and evolution of the system; these events, however, are unlikely to be preserved by the roll front, as a direct result of its hydrodynamic nature.

Probing silicate weathering reactions in soils with B isotopes

The determination of the mechanisms and extent of soil mineral weathering can be challenging, and the caveats reside in 1) difficulty identifying minerals that are actually involved in weathering reactions, 2) non-stoichiometric release of cations during weathering processes due to coupled dissolution, precipitation and transformation reactions and, 3) impact of vegetation activity on elemental cycles in upper soil horizons.To better characterize mechanisms controlling mineral weathering in soils and trace the evolution of B concentration and isotope ratios during chemical weathering, quantitative mineralogical analyses were coupled to B isotopes in a group of minerals (biotite, muscovite, K-feldspar and albite). Samples were selected along an Alocrisol (Alumic Cambisol, WRB FAO) soil profile from the bedrock (at 130 cm depth) up to 20 cm depth, developed on granitic bedrock in the Breuil-Chenue forest (France). The samples consist of residual primary minerals associated with weathering secondary phases (vermiculite, kaolinite…) in varying proportions.The B isotopic compositions of the most pristine minerals span a very narrow range of values (around −31‰), whereas all secondary phases point to a much heavier value (around −16‰), regardless of mineralogy. Our results also show a mineral-dependent evolution of B concentration or isotopic composition as weathering progresses: no variation is observed during dissolution of K-feldspars; B behaves like a very mobile element in micas (biotite and muscovite), whereas it concentrates in weathered products derived from albite. However, rates of B concentrations and changes in isotopic compositions appear to be much faster than those inferred from mineralogy or major element concentrations determined by XRD and bulk chemical analyses, respectively. These results indicate that B is involved in very early weathering reactions and raises the question of its actual location in the structure of the various soil minerals as well as its pathway to solution.

Variations in eastern Mediterranean hydrology during the last climatic cycle as inferred from neodymium isotopes in foraminifera

The Nd isotopic compositions (εNd) of mixed planktonic foraminifera have been analyzed in two sediment cores collected in the Nile deep-sea fan in order to reconstruct past εNd of the Eastern Mediterranean Deep Water (EMDW) and to assess the relative contributions of Nile discharge and Modified Atlantic Water (MAW) inflow to the Eastern Mediterranean Sea hydrology, as well as their potential control on anoxic events over the last climatic cycle. The two foraminiferal εNd records are similar and display an increase in εNd values during the African Humid Periods. Superimposed on this precession-forced variability (insolation received by the Earth at low latitudes), the record of variations in foraminiferal εNd indicates a 2-unit decrease in εNd during the interglacial Marine Isotope Stages (MIS) 5 and 1 compared to glacial MIS6, 4, 3 and 2. The εNd results suggest that the long-term glacial to interglacial changes in Nd isotopic composition of EMDW were not entirely induced by variations in Nile River discharge and Saharan dust inputs. Decreases in εNd during MIS5 and MIS1 interglacials indicate an increase in the contribution of unradiogenic MAW to the eastern Mediterranean Sea related to high sea-level stands and greater seawater exchange between the North Atlantic and Mediterranean basins. In addition, radiogenic seawater εNd values observed during African Humid Periods (and sapropel events) are associated with an intensification of Nile discharge and an increase in residence time of deep-water masses in the eastern Mediterranean Sea, which induces an increase in the interaction between deep-water masses and radiogenic sediments along the margin of the eastern Mediterranean Sea. Results confirm that an intensification of the hydrological exchanges between the western and eastern Mediterranean basins during high sea-level stand and the subsequent higher proportion of Atlantic Water in the Levantine Basin may have preconditioned the eastern Mediterranean Sea to sapropel depositions during the last climatic cycle.

New insights into the trophic ecology of young white sharks (Carcharodon carcharias) in waters off the Baja California Peninsula, Mexico

White sharks (Carcharodon carcharias) are described as generalist predators, with a demonstrated ontogenetic dietary shift which occurs between subadult and adult life stages. Trophic ecology studies on white shark have been focused mainly on large and mature individuals, necessitating studies of young white shark trophic ecology to better understand their resource use. This study provides new insights into young white shark diet in the North eastern Pacific Ocean using stable isotope analysis in muscle tissues. We analyzed δ13C and δ15N values of young white shark muscle (n = 21) from Sebastian Vizcaino Bay (SBV) during 2015–2018. We found changes in prey composition across early [neonates, young-of-the-years (YOYs), juveniles] white shark life stages, with significant changes in isotopic composition throughout early ontogeny. Mixing model results indicate a high use of coastal areas for foraging, mainly for juvenile stages and the substantial contribution of pelagic preys (e.g., S. japonicus, Prionotus spp., Cynoscion spp., S. sagax, etc.) in YOYs, white shark diet also indicates an important role of offshore foraging. This change in isotopic composition likely represents the shift from the embryo’s typical maternally derived isotopic signature, incorporated in offshore foraging regions, to the postpartum isotopic composition incorporated by foraging neonates in inshore nursery habitats. This study provides relevant information regarding young white shark feeding preferences, reinforces the importance of coastal areas as critical habitat for the development and the successful foraging of this species, and also provides indirect insights on the feeding habits of the adult female of white sharks, which constitutes a baseline for further research.

Isotopic Study of Springs Near Haditha Dam Western Iraq

Stable isotopic technique and hydrochemistry was used in studying the water resources interaction of near Haditha Reservoir area, western Iraq. Throughout the study area, 14 groundwater samples (Bashina, Zwachi springs and Wells), 8 surface water samples from the study area, and 7 spring samples were analyzed for 2H and 18O stable isotopes and hydrochemical analysis. In this study, the temperature, altitude and continental effects on the isotopic composition of rain water in Iraq were studied. The climate of the study area is classified as semi-arid to arid region. The results show a variation in the isotopic values of Haditha reservoir and Euphrates river. This variation is due to the effect of the low surface area and the low velocity of water of Haditha Reservoir on the amount of evaporation, compared with the high velocity and the large surface area of Euphrates river. There was a variation in the isotopic values between Bishina and Zwachi springs, due to two factors that appear to modify the isotopic signatures of the springs, namely the lack of hydraulic connection between the springs of Bishina and Zwachi, meaning that they recharge from different sources. The changes in oxygen isotope composition of the groundwater between a deep reservoir and the springs (Bishina) may be caused by the dilution with near surface waters (Haditha reservoir) with different oxygen isotope compositions. The variation in the isotopic content in the studied area indicated that there are various origins of springs recharge and a different interactions of the multiple sources of springs with the mutli-depths of springs water.

The triple oxygen isotope composition of Precambrian chert

The temperature and chemistry of early seawater have both been inferred from the isotopic composition of Precambrian chert (SiO2), a precipitated mineral formed on or within marine sediments. The δ18O of chert shows a robust quasi-linear increase through time - a signal that has been interpreted in a number of conflicting ways. For example, changing δ18O has been hypothesized to reflect the product of cooling surface ocean temperatures, a signature of evolving seawater δ18O composition, or the product of later stage diagenesis (where measured δ18O reflects the composition of diagenetic fluids). We suggest this uncertainty can be resolved through the additional measurement and interpretation of the minor oxygen isotope 17O (noted as Δ'17O) in conjunction with δ18O. In this study, we present a suite of triple oxygen isotope data on stratigraphically constrained Precambrian chert (both peritidal chert nodules in carbonates and iron formation silica). These mineralogically well-defined data allow for the first stratigraphic tests of the fidelity of 17O in SiO2. We then apply a Monte Carlo resampling technique to test the features of the competing hypotheses noted above, here now including critical constraints from 17O. The most parsimonious interpretation of these data suggests that secondary alteration with higher-temperature, meteoric-derived groundwater has skewed an original geochemical signature. This treatment can allow for some change in the oxygen isotope composition of seawater itself, however this does not appear to be the most statistically defensible single solution - clearly, some combination of multiple mechanisms is always possible and even likely. What is definitively the case is an equitable, modern-like Archean surface ocean temperature.

Changes in geochemical and carbon isotopic compositions during reactions of CO2-saturated groundwater with aquifer materials

This study evaluated impacts of CO2 leakage on a shallow groundwater system through laboratory column experiments, which simulated field push-and-pull and natural-gradient tests. The sediment and groundwater were collected from the Environmental Impact evaluation Test (EIT) facility in the Korea CO2 Storage Environmental Management (K-COSEM) test site, and temporal and spatial changes in aqueous chemistry at different stages were monitored. The results showed that as CO2-saturated groundwater was passing through the columns, the concentrations of cations, electrical conductivity (EC), and alkalinity increased, indicating dissolution of primary silicate minerals and perhaps trace amounts of undetected carbonate minerals. There was a significant difference in carbon-13 isotope ratios between the background and CO2-saturated groundwater, and isotopic composition change (with an enrichment factor of 1‰) occurred as CO2-saturated groundwater reacted with the aquifer materials. This study suggests that detailed temporal and spatial geochemical changes are helpful providing insights into the underlying geochemical mechanisms. Also, the isotopic fractionation modeling applied in this study is useful for detecting a small degree of carbon fractionation during the reactions of leaked CO2 and aquifer materials.

Hafnium isotopic record of mantle-crust interaction in an evolving continental magmatic system

Tracing the origin and evolution of magmas on their pathway through the lithosphere is key to understanding the magmatic processes that eventually produce eruptions. For ancient magmatic provinces, isotope-geochemical tracers are powerful tools to probe the source regions and magma-crust interaction during ascent and storage. Here we present hafnium isotopic compositions of ID-TIMS dated zircons to trace the evolution of the Middle Triassic magmatic province in the Southern Alps (northern Italy) at high temporal resolution. Systematic changes in hafnium isotopic composition with time record progressively stronger crustal assimilation over 3.5 million years, followed by a rapid increase in εHf towards more juvenile compositions for the major pulse of mafic intrusions and post-intrusive volcanic ash beds within one million years. We interpret these trends to reflect variations in mantle-crust interaction through time. Initial intrusions of basaltic dykes into the relatively cold lower crust cause only limited crustal melting and assimilation but an ensuing magma injection into progressively hotter crust results in more extensive partial melting and assimilation of crustal material. Subsequent intrusions into the magmatic lower-crustal roots cannibalize previous intrusions with progressively less isotopic contrast due to dilution with mantle-derived magmas. This is potentially accompanied by an increase in magma flux due to delamination of dense lower crustal cumulates into the subcontinental lithospheric mantle. The observed trends in hafnium isotopic composition therefore do not necessarily require tectonic re-organizations or changes in mantle sources. Instead these trends may trace variations in mantle-crust interaction during thermally induced chemical maturation of the lower crustal magmatic roots progressively replacing ancient pelitic to mafic lower crustal lithologies by juvenile cumulates.

The calcium isotopic composition of carbonate hardground cements: A new record of changes in ocean chemistry?

Reconstructing changes in the calcium isotopic composition (δ44Ca) of the ocean over Earth history has been challenging. This difficulty is due to the large range of calcium isotope fractionation factors during mineral precipitation and the potential for overwriting the initial δ44Ca of minerals during shallow marine diagenesis. We present a new δ44Ca record measured in carbonate hardground cements, an inorganic carbonate-mineral precipitate that rapidly forms at or near the sediment-water interface. The range in the δ44Ca for any particular carbonate hardground cements is between 0.05 and 0.56‰. In some cases, the progressive increase in the δ44Ca during precipitation can be observed, consistent with precipitation in a ‘closed-system’. Our data show an average calcium isotope fractionation during carbonate hardground cement precipitation that is −0.57 ± 0.27‰, similar to the calcium isotope fractionation factor for inorganic calcite precipitates in previous laboratory and modelling studies, and closer to what is considered a kinetic end member calcium isotope fractionation than growth at equilibrium. This is consistent with the rapid carbonate mineral precipitation expected for carbonate hardground cements. Our δ44Ca record over the Phanerozoic is similar to other calcium-bearing mineral records over the same time interval, with average δ44Ca becoming lower going back in time by about 0.5 to 0.7‰. Our results add further support for the evolution of seawater δ44Ca over time, and we discuss the possible causes of these changes with suggestions for future studies.

Authigenic carbonate burial in the Late Devonian–Early Mississippian Bakken Formation (Williston Basin, USA)

AbstractLate Devonian (Famennian) marine successions globally are typified by organic‐rich black shales deposited in anoxic and euxinic waters and the cessation of shelf carbonate sedimentation. This global ‘carbonate crisis’, known as the Hangenberg Event, coincides with a major extinction of reef‐building metazoans and perturbations to the global carbon cycle, evidenced by positive carbon‐isotope excursions of up to 4‰. It has been suggested that authigenic carbonate, formed as cements in sedimentary pore spaces during early burial diagenesis, is a significant mass fraction of the total global carbon burial flux, particularly during periods of low oxygen concentration. Because some authigenic carbonate could have originated from remineralization of organic carbon in sediments, it is possible for this reservoir to be isotopically depleted and thereby drive changes in the carbon isotopic composition of seawater. This study presents bulk isotopic and elemental analyses from fine‐grained siliciclastics of the Late Devonian–Early Mississippian Bakken Formation (Williston Basin, USA) to assess the volume and isotopic composition of carbonates in these sediments. Carbonate in the Bakken black shales occurs primarily as microscopic disseminated dolomite rhombs and calcite cements that, together, comprise a significant mass‐fraction (ca 9%). The elemental composition of the shales is indicative of a dynamic anoxic to sulphidic palaeoenvironment, likely supported by a fluctuating chemocline. Despite forming in an environment favourable to remineralization of organic matter and the precipitation of isotopically depleted authigenic carbonates, the majority of carbon isotope measurements of disseminated carbonate fall between −3‰ and +3‰, with systematically more depleted carbonates in the deeper‐water portions of the basin. Thus, although there is evidence for a significant total mass‐fraction of carbonate with contribution from remineralized organic matter, Bakken authigenic carbonates suggest that Famennian black shales are unlikely to be sufficiently 13C‐depleted relative to water column dissolved inorganic carbon to serve as a major lever on seawater isotopic composition.

Subcellular Chemical Imaging: New Avenues in Cell Biology.

To better understand the physiology and acclimation capability of the cell, one of the great challenges of the future is to access the interior of a cell and unveil its chemical landscape (composition and distribution of elements and molecules). Chemical imaging has greatly improved in sensitivity and spatial resolution to visualize and quantify nutrients, metabolites, toxic elements, and drugs in single cells at the subcellular level. This review aims to present the current potential of these emerging imaging technologies and to guide biologists towards a strategy for interrogating biological processes at the nanoscale. We also describe various solutions to combine multiple imaging techniques in a correlative way and provide perspectives and future directions for integrative subcellular imaging across different disciplines.

Changes in temperature and oxygen isotopic composition of Mediterranean water during the Mid-Pleistocene transition in the Montalbano Jonico section (southern Italy) using the clumped-isotope thermometer

Taking advantage of the recent clumped-isotope methodological developments, the present study focuses on the reconstruction of temperatures and seawater δ18O in the central Mediterranean Sea across the Mid-Pleistocene section from Montalbano Jonico (south of Italy). Our results suggest that Mg/Ca paleothermometer can be biased over several intervals, making clumped-isotope a promising choice to reconstruct past changes in seawater temperature and isotopic composition in the Mediterranean Sea. Our results provide the first clumped-isotope temperature and δ18OSW reconstruction across several glacial and interglacial Marine Isotope Stages from MIS 36 to MIS 19 in the central Mediterranean Sea.During the climatic optimums of MIS 31 and MIS 19, considered as close analogues to the current interglacial in terms of insolation forcing, reconstructed average sub-surface temperatures from benthic foraminifer analyses (13.8 ± 1.5 °C and 14.8 ± 1.3 °C, respectively) and isotopic composition of seawater (between 1.6 ± 0.4‰ and 2.0 ± 0.3‰) are similar to the ones measured today below the thermocline in the Gulf of Taranto. Our results show that bottom water conditions remained similar in all the studied glacial periods, with cold temperatures around ~ 8 °C in average. The lack of a clear cooling across the Mid-Pleistocene either suggest that glacial oceanographic conditions in the Mediterranean Sea remained relatively stable between the 41 ka-world and the 100 ka-world or that the tectonic uplift that took place during this transition balanced out the MPT cooling trend through the shallowing of the deposition site.

ГЛИНИСТІ МІНЕРАЛИ ЕОЦЕНОВОЇ КАМ’ЯНОЇ СОЛІ ФОРМАЦІЇ БАХАДАР ХЕЛЬ, ПАКИСТАН

According to studies of the pelitic fraction of the water-insoluble residue of 10 samples of Eocene rock salt of the Bahadur Khel Formation (Pakistan), it was determined that the clay minerals association contains swelling chlorite, chlorite-smectite, illite and kaolinite; chlorite was identified in three samples. Non-clay minerals are represented by quartz, dolomite, less often – magnesite; one sample contains impurities of both carbonates. Swelling chlorite, chlorite and mixed-layer minerals are trioctahedral, and illite and kaolinite are dioctahedral. All identified clay minerals, with the exception of kaolinite, are authigenic. The presence of swelling chlorite in Eocene rock salt is probably caused by changes in the concentration of brines in the basin against the background of complex geological processes of this era (climate change from thermal maximum to global cooling, changes in water circulation in oceans, changes in isotopic composition of carbonates). The association of clay minerals of Eocene rock salt, taking into account the peculiarities of its composition and the presence of swelling chlorite in it, we attributed to that formed during the SO4-rich seawater chemical type. This is also confirmed by two finds of swelling chlorite in the Triassic evaporites (rock salt of the Western Moroccan Basin, Midland marl) described in the literature, which are known to have been deposited from SO4-rich seawater. The presence of kaolinite in almost all samples is caused by its largest accumulation in sediments of this time period – terrigenous kaolinite came in large quantities from dry land and did not transform even at the stage halite precipitation. Full Text Keywords clay minerals, swelling chlorite, rock salt, Eocene, Bahadur Khel Salt, Pakistan.

Effects of temperature on food isotopic integrity and trophic fractionation in Chironomus riparius in laboratory experiments

Our experimental study was designed to assess the effects of temperature on food isotopic integrity and trophic fractionations (of carbon and nitrogen stable isotopes: Δ13C and Δ15N) in chironomid larvae. A laboratory experiment was run using Chironomus riparius larvae at 15, 18 and 23°C, and under three pulverized food resources. There were significant changes in the stable isotopic composition of the uneaten food, revealing the difficulty of preventing food microbial degradation in rearing experiments. C/N ratios of chironomid larvae were also affected by temperature, regardless of the food resource, suggesting changes in lipid contents and associated effects on the larval δ13C values. Therefore, differences in calculation methods (with vs. without lipid normalizations, fresh vs. old food isotopic baselines) induced large variability in Δ13C and Δ15N values, but our trophic fractionation estimates were similar to those previously reported in literature. Therefore, we conclude that temperature is not a major driver of the variability in trophic fractionations for chironomid larvae, and stable isotope composition of aquatic consumers can be used in food webs studies under changing temperature conditions. Variability in trophic fractionation estimates should, however, be considered to avoid misinterpretations of food web structure.

Effects of Farming Activities on the Temporal and Spatial Changes of Hydrogen and Oxygen Isotopes Present in Groundwater in the Hani Rice Terraces, Southwest China

Landform changes caused by human activities can directly affect the recharge of groundwater, and are reflected in the temporal and spatial changes in groundwater stable isotope composition. These changes are particularly evident in high-intensity farming areas. In this study, we tested and analyzed groundwater stable isotope samples at different elevations of rice terraces in a typical agricultural watershed of the Hani Terraces, a World Heritage Cultural Landscape in southwest China. Thus, we determined the characteristic variations and factors that influence the temporal and spatial effects on groundwater stable isotopes in the Hani Terraces, which are under the influence of high-intensity farming activities. The elevation gradients of δ18O and δ2H in groundwater are significantly increased due to farming activities. The values were 0.88‰ (100 m)−1 and −4.5‰ (100 m)−1, respectively, and they changed with time. The groundwater circulation cycle is approximately three months. We also used the special temporal and spatial variation characteristics of the groundwater isotopes as a way to evaluate the source and periodic changes of groundwater recharge. In addition, high-intensity rice farming activities, such as ploughing every year from October to January can increase the supply of terraced water to groundwater, thus ensuring the sustainability of rice cultivation in the terraces during the dry season. This demonstrates the role of human wisdom in the sustainable and benign transformation of surface cover and the regulation of groundwater circulation.

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).