Isotopes in Environmental and Health Studies最新文献

Radiogenic isotopes of igneous and detrital minerals from various clastic rocks of mountain belts are used to reveal tectonic and sedimentary processes, which are otherwise difficult to detect. Here, we discuss the results of U-Pb and Lu-Hf zircon systems, and ⁴⁰Ar/³⁹Ar on detrital white mica in Eastern Alps. Zircon and white mica are chemically and mechanically stable and occur in magmatic, metamorphic and sedimentary rocks. During subsequent metamorphism, zircon is resistant against high temperature, >650 °C (U-Pb) and 900 °C (Lu-Hf). The Lu-Hf zircon system is used as a tracer of initial magma separation from the mantle, and the U-Pb zircon system records magmatic crystallization. The ⁴⁰Ar/³⁹Ar white mica system is stable up to 400-450 °C dating either formation or cooling after high-grade metamorphism. Detrital U-Pb zircon ages on two major rivers draining the Eastern Alps do not record any sign of Alpine orogeny or metamorphism. Consequently, U-Pb zircon studies can entirely miss the record of collisional orogeny in cool, magma-poor collision orogens. In contrast, ⁴⁰Ar/³⁹Ar white mica ages record Early and Late Alpine metamorphism but are limited to revealing the pre-orogenic history. U-Pb zircon and ⁴⁰Ar/³⁹Ar white mica yield different information in provenance studies. In the Eastern Alps, U-Pb zircon dating of magmatic and clastic rocks indicates intense formation of magmatic rocks between 630 and 230 Ma. Felsic rocks dominate the older age groups, and increasingly young mafic rocks were dated, specifically between 265 and 230 Ma. Hf isotopes record increasing juvenile input since ∼630 Ma. Two different groups with respect to Mesoproterozoic depleted mantle ages are shown: (1) one group with a Mesoproterozoic age gap typical for Gondwana-derived units, and (2) a rare group with Mesoproterozoic ages recording a new tectonic element in the Austroalpine basement in Alps.

Stable isotopes of chlorine have great application potential due to the widespread occurrence of the chlorine anion in water, minerals, living organisms and the environment. In most studies, the chloride ion from the samples is converted to chloromethane, which is then analysed isotopically using a mass spectrometer. In the present study, a new design for a chloromethane preparation line is proposed. In particular, the new chloromethane preparation line uses a new system for injecting iodomethane into the preparation system, as well as ampoules with Teflon valves and the u-shaped freezers. These improvements reduced the preparation time to about 1 h, and also achieved a decent measurement uncertainty of 0.05 permil.

For a detailed characterization of the 5.7 10⁶ mt phosphogypsum (PG) stack in the vicinity of Bacau city, Romania, the air dose rate (ADR) was measured in 72 points covering the stack surface, while 10 samples of stack material were collected for future analysis. Radiometric determinations showed for the ADR values varying between 364 ± 53 and 489 ± 8 nSv/h, with some extreme values of 2775 ± 734 nSv/h, significantly exceeding 90 nSv/h, the average value reported for the Romanian territory. High-resolution gamma-ray spectroscopy (HRGS), performed on 10 samples collected from the entire PG stack evidenced only the presence of ²²⁶Ra as the major radioactive element with a specific activity varied between 820 ± 150 and 5278 ± 264 Bq/kg for hot spots. Further analysis performed on a similar number of samples by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), X-ray fluorescence (XRF), scanning electron microscopy (SEM) and energy dispersive X-ray spectrometry (EDX), evidenced, beside gypsum as the main component, traces of brushite (CaHPO₄·2H₂O) and ardealite (Ca₂(PO₃OH)(SO₄)·4H₂O), as well as the presence of small acicular celestine (SrSO₄) agglomerates. XRF determinations of the mass fractions of major elements evidenced values such as SiO₂ (2.31 ± 0.73 %), TiO₂ (0.07 ± 0.01 %), Al₂O₃ (0.17 ± 0.04 %), Fe₂O₃ (0.87 ± 0.18 %), MnO (0.01 ± 0.01 %), MgO (0.17 ± 0.02 %), CaO (32.5 ± 0.82 %), Na₂O (0.04 ± 0.04 %), K₂O (0.05 ± 0.01 %), P₂O₅ (2.12 ± 0.51 %), LOI (20.2 ± 0.3 %), i.e. closer to literature reported data for PG of different provenience while the data concerning the distribution of 20 trace elements, including incompatible Sc, La, Ce, and Th were relatively closer to the upper continental crust (UCC).

Comparing and combining stable isotope datasets from different laboratories and different years is essential for many research areas, such as isotope hydrology, greenhouse gas observations, food studies, isotope forensics, palaeo-reconstructions, etc. Data compatibility (i.e. the ability to combine data) is related to the data quality. The prerequisite for data comparability is data normalization to a common stable isotope scale (often referred to as calibration) based on reliable reference materials (RMs) with accurately assigned values and uncertainties. Still, that does not guarantee the data compatibility (mutual agreement). Albeit metrological concepts related to data compatibility and measurement uncertainty have been developed and applied to analytical chemistry in general, these concepts have not yet been fully applied to stable isotope research. This can affect daily calibrations, analytical data and, therefore, data compatibility. In addition, IRMS users often prepare different laboratory standards themselves. Thereafter, users should then understand the contemporary concepts used for assigning RM value and uncertainty, as well as the limitations and potential problems associated with RMs. The history of RMs, preparation reports and also some problems in the past provide lessons to be learned. These include the δ¹³C drift of LSVEC (the second anchor on the δ¹³C scale before 2017), revisions to the value assignment principles, the introduction of replacements for LSVEC, related disputes and the potential underestimation of uncertainties for secondary RMs. The review describes metrological concepts related to isotopic scales, RMs and calibration hierarchies and data compatibility. The main RMs and their uncertainties are reviewed through the lens of metrology concepts. Additional focus is given to the VPDB scale for δ¹³C and issues of scale discontinuity, which can significantly reduce data compatibility in δ¹³C. The given examples of value and uncertainty assignment for RMs should be viewed as an example of value and uncertainty calculation in daily practice.

The Lower Quang Tri River Group, situated in central Vietnam, faces a myriad of challenges, notably the decline in groundwater levels and the salinisation of both groundwater and surface water, significantly impacting water availability for domestic, agricultural, and industrial purposes. To address these pressing concerns, this study adopts a comprehensive methodology integrating hydrogeological measurements, isotopic techniques, and chemical analyses of various water sources, including local precipitation, surface water bodies, reservoirs, and groundwater samples. Utilising the deuterium and oxygen-18 signatures (δ²H and δ¹⁸O) in water molecules as environmental tracers for the assessment of base flow and water sources enables a nuanced understanding of the intricate interaction between surface water and groundwater. Research findings elucidate that during the dry season, groundwater recharge primarily stems from water in the reservoirs over approximately seven months. Base flow contributes between 80 and 85 % of streamflow during the rainy season, escalating to 100 % during the dry season. The mean travelling time of the base flow is estimated at 120 ± 10 days using the sine curve model developed by Rodgers et al. The insights gleaned from this study are poised to play a pivotal role in guiding the local water resources managers in licensing for the exploitation of a right quantities of groundwater as sustainable management strategies in the region.

Isotope source tracing enables to accurately determine the fate of nutrients that are applied with fertilizers to soils. While this approach is well established for major nutrients such as nitrogen, it is not yet established for trace metals. Here, we aimed to determine the fate of the micronutrient zinc (Zn) and the contaminant cadmium (Cd) that were applied with an organic fertilizer to a soil-wheat system. A pot study was conducted in which wheat was grown on an alkaline soil. The soils received green manure and/or soluble Zn fertilizer and were compared with non-fertilized control treatments (n = 4 experimental replicates). The green manure was labelled with the stable isotopes ⁶⁷Zn and ¹¹¹Cd. For an efficient sample throughput, a method was provided and validated to determine enriched stable isotope ratios (⁶⁷Zn:⁶⁶Zn and ¹¹¹Cd:¹¹⁰Cd) and the Zn and Cd concentrations in one analytical run. To this end, single collector ICP-MS analyses and stable isotope mass balances calculations were combined. Applying this method revealed that the addition of green manure increased neither Zn nor Cd concentrations in wheat grains due to biomass dilution effects. Isotope source tracing showed that the largest fraction of these metals in the wheat shoots derived from the soil in all treatments (Zn 87-99 %, Cd 94-98 %). Moreover, the addition of green manure increased the transfer of Zn and Cd from soil to wheat by a factor 1.9 for both elements. This increased transfer was likely related to a nitrogen fertilization effect that increased root and shoot biomass and thereby the soil exploration of the wheat. This study demonstrated how the fate and dynamics of multiple trace metals can be efficiently determined in soil-fertilizer-crop systems using isotope source tracing.

We studied δ¹³C, δ¹⁵N and δ¹⁸O values, and total mercury (THg) concentrations in muscle samples from deep-sea predators - five beaked whale species and sperm whales - stranded along the coast of Hokkaido, in the north of Japan in 2010 and 2019. The δ¹³C, δ¹⁵N and δ¹⁸O values, THg concentrations, and body length (BL) of Stejneger's beaked whales were similar to those of Hubbs' beaked whales, which belong to the same genus. In contrast, δ¹³C values, THg concentrations, and BL of Sato's beaked whales were markedly different from those of Baird's beaked whales, which belong to the same genus. Stejneger's and Hubbs' beaked whales living around Hokkaido may compete in their ecological niches, whereas Sato's and Baird's beaked whales may segregate their ecological niches. Although Cuvier's beaked whales and sperm whales belong to different genera and their BLs were significantly different, their δ¹³C and δ¹⁵N values were similar, probably because they can dive and stay in deeper waters than other beaked whale species. The δ¹³C values in combined samples from all whales increased with increasing BL, probably owing to the larger whale species' dietary preference for squid. The δ¹³C values in combined samples from all whales were positively correlated with THg concentrations, whereas the δ¹⁵N values in the combined samples were negatively correlated. The δ¹⁸O values in combined samples from most whales tended to be positively correlated with THg concentrations. These correlations may be explained by a higher THg load from deep-sea feeding than from pelagic feeding and by a feeding shift towards lower trophic levels.

The application of stable isotope analysis (SIA) to the fields of ecology and animal biology has rapidly expanded over the past three decades, particularly with regards to water analysis. SIA now provides the opportunity to monitor migration patterns, examine food webs, and assess habitat changes in current and past study systems. While carbon and nitrogen SIA of biological samples have become common, analyses of oxygen or hydrogen are used more sparingly despite their promising utility for tracing water sources and animal metabolism. Common ecological applications of oxygen or hydrogen SIA require injecting enriched isotope tracers. As such, methods for processing and analyzing biological samples are tailored for enriched tracer techniques, which require lower precision than other techniques given the large signal-to-noise ratio of the data. However, instrumentation advancements are creating new opportunities to expand the applications of high-throughput oxygen and hydrogen SIA. To support these applications, we update methods to distill and measure water derived from biological samples with consistent precision equal to, or better than, ± 0.1 ‰ for δ¹⁷O, ± 0.3 ‰ for δ¹⁸O, ± 1 ‰ for δ²H, ± 2 ‰ for d-excess, and ± 15 per meg for Δ¹⁷O.

Terrestrial gamma radiation is one of the major outdoor radiation exposures to the general public that varies substantially based on the type and geological properties of the soil. The objective of this study is to evaluate the naturally occurring radioactive materials (NORMs) distribution and assess the hazard parameters in the riverbank soil within various industrial zones in the densely populated Dhaka and Chattogram cities of Bangladesh. The mean activities of ²²⁶Ra (37 ± 3), ²³²Th (58 ± 4), and ⁴⁰K (1129 ± 18) Bqkg^-1 in the assessed soil samples were found to be slightly higher than the world average values 32, 35, and 420 Bqkg^-1, respectively. The mean radium equivalent activity (207.49 Bqkg^-1) and the external and internal hazard indices were within the recommended limits of 370 Bqkg^-1 and <1, respectively. The mean absorbed dose rate (99.47 nGyhr^-1), annual effective dose (0.12 mSva^-1), ELCR (4.27 × 10^-4), and gamma level index (1.58) exceeded the world average values 59 nGyhr^-1, 0.07 mSva^-1, 2.9 × 10^-4, and 1 respectively. However, the studied areas are safe from a radiological viewpoint with no radiation health hazard to the people. The results of this study can be utilized to produce factual baseline data for future studies.