Factors controlling carbon isotope ratios of dissolved inorganic carbon in two major tributaries of the Han River,Korea

Understanding the carbon cycle of the Han River system in Korea is of prime interest in managing and preserving this valuable water resource for more than 20 million residents in the area. As a part of a comprehensive carbon cycling study for the Han River system, this report focuses on the carbon isotope compositions of dissolved inorganic carbon (DIC) in its two major tributaries, the North and the South Han Rivers. The major difference in carbonate chemistry of the tributaries originates primarily from the lithology of the catchment areas. The South Han River, draining a carbonate‐dominant terrain, has much higher alkalinities and DIC concentrations, whereas the lower concentrations in the North Han River indicate little influence of carbonate weathering. Likewise, δ¹³C_DIC values in the South Han River indicate that the DIC input from the carbonate rocks is important in controlling carbon isotope ratios of DIC. For the North Han River, the oxidation of organic material influences the amount of riverine DIC and δ¹³C_DIC values to a greater extent. Overall, remarkable seasonal and spatial variations of river chemistry and carbon isotope compositions of DIC reflect the variability in geo‐hydrologic characteristics, in the water regime, and in metabolic activities in the river water and/or the drainage areas. Copyright © 2006 John Wiley & Sons, Ltd.     

淮南采煤沉陷区积水水文地球化学及氢氧稳定同位素特征

以安徽淮南采煤沉陷积水为研究对象,通过样品采集与测试,研究不同沉陷年限及类型积水水文地球化学和氢氧稳定同位素组成特征及影响因素.结果表明：（1）研究区水化学类型主要为Cl-Na、HCO₃·Cl-Na型,沉陷积水中常量离子主要来源于蒸发岩溶解和硅酸盐风化,受蒸发作用和人为活动的影响明显,水化学组成随沉陷时间和类型变化不大.（2）淮南大气降水线方程为：δD=8.85δ¹⁸O+18.73,沉陷区积水氢氧稳定同位素值在淮南大气降水线右下方依次分布并接近降水线,表明沉陷积水主要来源于大气降水.（3）在降水稀释、水体蒸发及地下水补给的作用下,随着沉陷年限的增加,积水中重同位素越来越贫化,同一年限不同类型的积水同位素值变化较小.     

Differing controls on river‐ and lake‐water hydrogen and oxygen isotopic values in the western United States

Surface water oxygen and hydrogen isotopic values are commonly used as proxies of precipitation isotopic values to track modern hydrologic processes while proxies of water isotopic values preserved in lake and river sediments are used for paleoclimate and paleoaltimetry studies. Previous work has been able to explain variability in USA river‐water and meteoric‐precipitation oxygen isotope variability with geographic variables. These studies show that in the western United States, river‐water isotopic values are depleted relative to precipitation values. In comparison, the controls on lake‐water isotopic values are not well constrained. It has been documented that western United States lake‐water input values, unlike river water, reflect the monthly weighted mean isotopic value of precipitation. To understand the differing controls on lake‐ and river‐water isotopic values in the western United States, we examine the seasonal distribution of precipitation, evaporation and snowmelt across a range of seasonality regimes. We generate new predictive equations based on easily measured factors for western United States lake‐water, which are able to explain 69–63% of the variability in lake‐water hydrogen and oxygen isotopic values. In addition to the geographic factors that can explain river and precipitation values, lake‐water isotopic values need factors related to local hydrologic and climatic characteristics to explain variability. Study results suggest that the spring snowmelt runs off the landscape via rivers and streams, depleting river and stream‐water isotopic values. By contrast, lakes receive seasonal contributions of precipitation in proportion to the seasonal fraction of total annual precipitation within their watershed. Climate change may alter the ratio of snow to rain fall, affecting water resource partitioning between rivers and lakes and by implication of groundwater. Paleolimnological studies must account for the multiple drivers of water isotopic values; likewise, studies based on the isotopic composition of fossil material need to distinguish between species that are associated with rivers versus lakes. Copyright © 2010 John Wiley & Sons, Ltd.     

Spatial,seasonal, and source variability in the stable oxygen and hydrogen isotopic composition of tap waters throughout the USA

To assess spatial, seasonal, and source variability in stable isotopic composition of human drinking waters throughout the entire USA, we have constructed a database of δ¹⁸O and δ²H of US tap waters. An additional purpose was to create a publicly available dataset useful for evaluating the forensic applicability of these isotopes for human tissue source geolocation. Samples were obtained at 349 sites, from diverse population centres, grouped by surface hydrologic units for regional comparisons. Samples were taken concurrently during two contrasting seasons, summer and winter. Source supply (surface, groundwater, mixed, and cistern) and system (public and private) types were noted. The isotopic composition of tap waters exhibits large spatial and regional variation within each season as well as significant at‐site differences between seasons at many locations, consistent with patterns found in environmental (river and precipitation) waters deriving from hydrologic processes influenced by geographic factors. However, anthropogenic factors, such as the population of a tap's surrounding community and local availability from diverse sources, also influence the isotopic composition of tap waters. Even within a locale as small as a single metropolitan area, tap waters with greatly differing isotopic compositions can be found, so that tap water within a region may not exhibit the spatial or temporal coherence predicted for environmental water. Such heterogeneities can be confounding factors when attempting forensic inference of source water location, and they underscore the necessity of measurements, not just predictions, with which to characterize the isotopic composition of regional tap waters. Published 2013. This article is a U.S. Government work and is in the public domain in the USA.     

Temporal variation of stable isotopes in a precipitation–groundwater system: implications for determining the mechanism of groundwater recharge in high mountain–hills of the Loess Plateau,China

The groundwater in shallow loess aquifers in high mountain–hills in the western Loess Plateau in China is almost the sole water resource for local residents. However, the question about how the loess groundwater naturally circulates in these high mountain–hills, characterized by low precipitation and high potential evaporation, remains unclear. The objectives of this study are to evaluate the application of hydrogen and oxygen isotopes to (1) examine temporal variations of the isotopic composition of precipitation and shallow groundwater and (2) uncover the mechanism of groundwater recharge in high mountain–hills. Results from 2 years of monitoring data show a difference in the stable isotopes for groundwater and local precipitation between the winter and summer periods. Similar to precipitation, stable isotopes in groundwater are observed to be depleted in winter and enriched in summer, particularly in oxygen isotope. A prominent characteristic is that H and O isotopes of groundwater show a very clear response to strong precipitation in the rainy season in 2013. The results highlight that local precipitation is the likely recharge source for groundwater in shallow loess aquifers. Annual recharge from local precipitation maintains the groundwater resource in the shallower loess aquifer. The mechanisms governing shallow loess groundwater recharge in high mountain–hills were evaluated. In addition to possible vertical slow percolation of soil water through the unsaturated zone, rapid groundwater recharge mechanisms have been identified as temporal preferential infiltration through sinkholes, slip surface or landslide surface and through the interface of loess layer and palaeo‐soils. Most groundwater can be recharged after a heavy rainy season. Copyright © 2015 John Wiley & Sons, Ltd.     

Origin and chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta,Botswana

The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ¹⁸O and δ¹³C_DIC). The δD and δ¹⁸O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO₃ type and the deep (≥10 m) groundwater is Na–K–HCO₃ to HCO₃–Cl–SO₄ to Cl–SO₄–HCO₃. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ¹³C_DIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.     

Evolution and variation of the Tsushima warm current during the late Quaternary: Evidence from planktonic foraminifera, oxygen and carbon isotopes

The evolution and variation history of the Tsushima warm current during the late Quaternary was reconstructed based on the quantitative census data of planktonic foraminiferal fauna, together with oxygen and carbon isotope records of mixed layer dweller G. ruber and thermocline dweller N. dutertrei in piston core CSH1 and core DGKS9603 collected separately from the Tsushima warm current and the Kuroshio dominated area. The result showed that the Tsushima warm current vanished in the lowstand period during 40―24 cal ka BP, while the Kuroshio still flowed across the Okinawa Trough, arousing strong upwelling in the northern Trough. Meanwhile, the influence of freshwater greatly increased in the northern Okinawa Trough, as the broad East China Sea continental shelf emerged. The freshwater reached its maximum during the last glacial maximum (LGM), when the upwelling obviously weakened for the lowest sea-level and the depression of the Kuroshio. The modern Tsushima warm current began its development since 16 cal ka BP, and the impact of the Kuroshio increased in the middle and north- ern Okinawa Trough synchronously during the deglaciation and gradually evolved as the main water source of the Tsushima current. The modern Tsushima current finally formed at about 8.5 cal ka BP, since then the circulation structure has been relatively stable. The water of the modern Tsushima cur- rent primarily came from the Kuroshio axis. A short-term wiggle of the current occurred at about 3 cal ka BP, probably for the influences from the enhancement of the winter monsoon and the depression of the Kuroshio. The cold water masses greatly strengthened during the wiggle.     

Stable isotope ratios of carbon,nitrogen and oxygen in killer whales (Orcinus orca) stranded on the coast of Hokkaido,Japan

We analyzed δ¹³C, δ¹⁵N and δ¹⁸O in the muscle and liver from killer whales stranded on the coast of Japan. The δ¹⁵N values in the muscle samples from calves were apparently higher than those in their lactating mothers, suggesting that nursing may result in the higher δ¹⁵N values in the muscle samples of calves. The δ¹⁵N value in the muscle samples of male and female whales, except for the calves, were positively correlated with the δ¹³C values and body length, suggesting that the increases in δ¹⁵N were due to the growth of the whales and increase in their trophic level. In contrast, the δ¹⁸O values in the muscle samples of female whales except for the calves were negatively correlated with the δ¹³C and δ¹⁵N values. The δ¹⁸O may be lower in whales occupying higher trophic positions (δ¹⁵N), although it might also be affected by geographic and climatic conditions.     

Comparison of C and N stable isotope ratios between surface particulate organic matter and microphytoplankton in the Gulf of Lions (NW Mediterranean)

Carbon and nitrogen stable isotope ratios of particulate organic matter (POM) in surface water and 63–200 μm-sized microphytoplankton collected at the fluorescence maximum were studied in four sites in the Gulf of Lions (NW Mediterranean), a marine area influenced by the Rhone River inputs, in May and November 2004. Some environmental (temperature, salinity) and biological (POM, Chlorophyll a and phaeopigments contents, phytoplankton biomass and composition) parameters were also analysed. Significantly different C and N isotopic signatures between surface water POM and microphytoplankton were recorded in all sites and seasons. Surface water POM presented systematically lower δ¹³C (∼4.2‰) and higher δ¹⁵N (∼2.8‰) values than those of microphytoplankton, due to a higher content of continental and detrital material. Seasonal variations were observed for all environmental and biological parameters, except salinity. Water temperature was lower in May than in November, the fluorescence maximum was located deeper and the Chlorophyll a content and the phytoplankton biomass were higher, along with low PON/Chl a ratio, corresponding to spring bloom conditions. At all sites and seasons, diatoms dominated the phytoplankton community in abundance, whereas dinoflagellate importance increased in autumn particularly in coastal sites. C and N isotopic signatures of phytoplankton did not vary with season. However, the δ¹⁵N of surface water POM was significantly higher in November than in May in all sites likely in relation to an increase in ¹⁵N/¹⁴N ratio of the Rhone River POM which influenced surface water in the Gulf of Lions. As it is important to determine true baseline values of primary producers for analysing marine food webs, this study demonstrated that C and N isotopic values of surface water POM cannot be used as phytoplankton proxy in coastal areas submitted to high river inputs.     

A comparison of peak and plate electrodes in electrical resistivity tomography: application to the chalky groundwater of the Beauvais aquifer (northern part of the Paris basin,France)

Electrical resistivity tomography was used in order to explore an experimental site of the LaSalle Beauvais Polytechnic Institute (France). The test was conducted along a profile line of 315 m length, using 64 electrodes deployed at an inter‐electrode spacing of 5 m, and the data were recorded using gradient, Wenner and pole–dipole arrays. The performance of plate electrodes (non‐conventional flat‐based) is compared with the performance of peak electrodes (conventional spike). The hydrogeophysical investigation of the chalk aquifer system of Beauvais shows that the performance of plate electrodes is satisfactory, leading to inversions of small root‐mean‐square errors. Peak and the plate electrodes were tested before and after injection of a salt tracer in the piezometer of the experimental site. The study demonstrates the usefulness of plate electrodes (efficient, less time consuming) and the possibility of aquifer characterization by a salt tracer. Copyright © 2010 John Wiley & Sons, Ltd.