Seasonal variation in end-members and discharge mechanisms of a caldera spring with multiple groundwater flow systems: insights from multi-tracer analysis in the Aso Caldera, Japan

Short-term (0.5–3 d) precipitation samples were collected from January 1992 to December 2001 in Calgary, Alberta, Canada, and the stable isotope ratios of hydrogen (2H/1H) and oxygen (18O/16O) for these samples were determined. The 10-yr amount-weighted average δ2H and δ18O values of precipitation were −136.1° and −17.9°, respectively. Consistent with International Atomic Energy Agency (IAEA) established practice, the following local meteoric water line (LMWL) for Calgary was derived using amount-weighted monthly average δ2H and δ18O values: δ2H = 7.68 δ18O −0.21 (r2= 0.96, n= 104). The correlation equation between δ2H and δ18O values from individual samples was found to be δ2H = 7.10 δ18O −13.64 (r2= 0.95, n= 839), which is different from the LMWL, exhibiting lower slope and intercept values. A comparison of δ2H and δ18O correlation equations with temperature during precipitation events showed a trend of decreasing slopes and intercepts with increasing temperature. Our data suggest that this is caused by incorporation of moisture derived from evaporation from water bodies and soils along the storm paths and by secondary evaporation between the cloud base and the ground during precipitation events. These processes compromise the usefulness of d-excess values as an indicator for the meteorological conditions in the maritime source regions. The δ18O temperature dependence at Calgary was found to be ⊼ 0.44°¼C−1. The study shows that short-term sampling of individual precipitation events yields valuable information, which is not obtainable by the widely used monthly collection programs.

To clarify the determining processes of stable isotope ratios of hydrogen (δD) and oxygen (δ18O) in paddy water and the factors affecting them, we collected irrigated water, drain water, and ponded water in mid-May, early in June, and at the beginning of August in 2002 from a paddy field, where intensive measurement of water balance was performed. The values of δD and δ18O gradually increased along the flow direction of paddy water. In a δ18O vs. δD diagram, these data were plotted linearly for each month, and the slopes ranged from 4.3 to 5.8, showing kinetic isotope fractionation during evaporation. In August, the increase of δ values was much less than that in May and June, while the slope of evaporation line (SEL) was largest. Considering evaporative fractionation based on the Craig-Gordon model, the large SEL in August resulted from limited kinetic fractionation due to high humidity under a grown rice canopy. The grown canopy would also lower the increase of δ values by restricting evaporation. At the beginning of August, however, rainfall from a thunderstorm and the change of irrigation management also influenced δ values, so the lowered δ-increase was not attributed only to the restriction of evaporation. The result of the study shows the possibility to separate evaporation and transpiration using isotope hydrological approaches, which is usually impossible by micrometeorological direct measurements.

Water quality, stable isotope ratios of hydrogen and oxygen (δ18O and δ D) and temperature-depth profile in the Chikushi Plain were examined by field observations and chemical analysis in 2004 and 2005. Water samples for chemical analysis were collected from observation wells, pumping wells, rivers and springs.

We measured major inorganic ions and stable isotope ratios of nitrogen and oxygen of nitrate in the stream water in the Chichibu region during the course of nitrogen saturation. Nitrate concentration showed a high west-east gradient in the study area. Stable isotope ratios of oxygen in nitrate showed clear relationships with nitrate concentration. A direct relationship was apparent in the lower range of nitrate concentrations in that the stable isotope ratio of oxygen increases as the nitrate concentration increases. On the other hand, oxygen stable isotope ratios of nitrate hardly increase in the middle to higher concentrations of nitrate. This phenomenon may suggest that the oxygen stable isotope ratios of nitrate reflect a phase of the nitrogen saturation in the forest ecosystems.

Stable isotope studies on stable isotope ratios of hydrogen and oxygen in water within plants provide new information on water sources and water use patterns under natural conditions. In this study, the sources of water uptake for two typical xerophytic shrubs, Caragana korshinskii and Artemisia ordosica, were determined at four different-aged revegetated sites (1956, 1964, 1981, and 1987) in the Tengger Desert, a revegetated desert area in China. Samples from precipitation, soil water at different soil layers, and xylem water from each species were collected in 2013. The proportion of plant water sources derived from different potential sources was determined using oxygen (δ18O) and hydrogen (δD) stable isotope analysis combined with a multiple-source linear mixing model. Results showed that the local meteoric water line (LMWL) at Shapotou was as follows: δD = 7.39δ18O + 3.91 (R2 = 0.93; n = 26). The vertical distribution of soil water content in older vegetation areas (1956a and 1964a) was much lower than that in relatively younger vegetation areas (1981a and 1987a). Mean soil water δD and δ18O values varied with depth, and the variation decreased as the age of the revegetated site increased. In general, C. korshinskii and A. ordosica mainly tapped water from the upper soil layer (10–100 cm) during the wet seasons. With increasing sand stabilization age, the proportion of water sources from shallow soil water decreased, whereas deep soil moisture utilization increased. During the dry season, C. korshinskii and A. ordosica showed evident hierarchical utilization of soil water in different soil layers. Small rainfall events did not significantly affect the water source of C. korshinskii and A. ordosica. However, large rainfall events not only complemented the deep soil moisture, but also recharged the shallow soil water after a few days, and the proportion of soil water source from deep soil layer increased from 2% ± 0.7% to 10% ± 1.4% for both plants.

Stable isotope ratios of hydrogen and oxygen (δ2H and δ18O) in tap water provide important insights into the way that people interact with and manage the hydrological cycle. Understanding how these interactions vary through space and time allows for the management of these resources to be improved, and for isotope data to be useful in other disciplines. The seasonal variation of δ2H and δ18O in tap water within South Africa was assessed to identify municipalities that are supplied by seasonally invariant sources that have long residence periods, such as groundwater, and those supplied by sources that vary seasonally in a manner consistent with evapoconcentration, such as surface water—the proposed two tap water “worlds”. Doing so allows for the cost-effective spatial interpolation of δ2H and δ18O values that likely reflect that of groundwater, removing the residual error introduced by other sources that are dependent on discrete, isolated factors that cannot be spatially generalised. Applying the proposed disaggregation may also allow for the efficient identification of municipalities that are dependent on highly variable or depleted surface water resources, which are more likely to be vulnerable to climate and demographic changes.

As is the case for carbon, the study of stable hydrogen and oxygen isotopes in plant matter has its origins in the field of geochemistry. Geochemists for some time have been interested in using stable hydrogen and oxygen isotope ratios in fossil plant matter to determine climate during the formation of the plant matter in question. They reasoned that since the oxygen and hydrogen isotope ratios of water available for incorporation into plant biomass is influenced by climate, then the hydrogen and oxygen isotope ratios of plant matter should also be determined by climate. To determine climate, it would only be a question of deciphering the isotopic fractionation steps from water entering the roots to cellulose synthesized in the leaves.KeywordsIsotope RatioOxygen IsotopeLeaf WaterIsotopic FractionationCrassulacean Acid MetabolismThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

The stable isotope ratios of oxygen, hydrogen, carbon and sulfur from extracted wood of 87 samples of oaks from the United States were analysed. Relationships with climate variables and the stable isotope ratios of the 69 training dataset samples were investigated to a monthly resolution using long-term monthly mean climate data from NASA and the University of East Anglia’s Climate Research Unit, in conjunction with forecast data for hydrogen and oxygen isotope ratios in precipitation. These relationships were used to construct model isoscapes for oxygen, hydrogen, carbon and sulfur for US oak with the aim of using them to forecast isotopic patterns in areas that were not sampled and predict values in samples not used to construct the models. The leading predictors for isoscape generation were oxygen isotope ratios in January precipitation for oak oxygen isotope ratios, hydrogen isotope ratios in July precipitation for oak hydrogen isotope ratios, water vapour in April for carbon isotope ratios, and reflected shortwave radiation in March in combination with sulfate concentration in May for oak sulfur isotopes. The generated isoscapes can be used to show regions an unknown sample may have originated from with a resolution dependent on the rarity of the stable isotope signature within the United States. The models were assessed using the data of 18 samples of georeferenced oak. The assessment found that 100% of oxygen, 94% of hydrogen, 78% of carbon, and 94% of sulfur isotope ratios in the 18 test dataset samples fell within two standard deviations of the isoscape models. Using the results of the isoscapes in combination found that there were 4/18 test samples which did not fall within two standard deviations of the four models, this is largely attributed to the lower predictive power of the carbon isoscape model in conjunction with high local variability in carbon isotope ratios in both the test and training data. The method by which this geographic origin method has been developed will be useful to combat illegal logging and to validate legal supply chains for the purpose of good practice due diligence.

Geographical discrimination of mulberry leaves is very important for their efficacy and quality as a traditional Chinese medicine. Stable hydrogen, oxygen, and carbon isotope ratios were measured in 292 mulberry leaves collected at 2 growth stages in 2 seasons from 8 regions of China. A stepwise linear discriminant analysis (LDA) approach were proposed to combine with stable isotope technology to tracing the origin of mulberry leaves. The results showed that leaves sampled in autumn were extremely depleted in 2H and 18O and slightly enriched in 13C compared with leaves sampled in summer, correlated with the effect of season, transpiration and photorespiration on stable isotopes. δ2H and δ18O of the leaves were enriched during the growth process. The overall discrimination accuracy of the autumn tender model was 81%, demonstrating that analysis of δ2H, δ18O, and δ13C is a promising technique for tracing the geographical origin of mulberry leaves, although season, growth stage and number of samples affect the accuracy of discrimination.

Tropical seasonality in the late Campanian (late Cretaceous): Comparison between multiproxy records from three bivalve taxa from Oman

: Increasingly, hydrologic studies require information on the isotopic composition of natural waters. This report presents stable hydrogen (delta2H) and oxygen isotope ratios (delta18O) from 391 selected sites of the U.S. Geological Survey's National Stream Quality Accounting Network (NASQAN) and BENCHMARK surface water networks collected during the years 1984 1987. Depth-integrated samples were collected and analyzed from each site bimonthly or quarterly for about 3 years.

Abstract. About 80 % of the precipitation at the Colorado River's headwaters is snow, and the resulting snowmelt-driven hydrograph is a crucial water source for about 40 million people. Snowmelt from alpine and subalpine snowpack contributes substantially to groundwater recharge and river flow. However, the dynamics of snowmelt progression are not well understood because observations of the high-elevation snowpack are difficult due to challenging access in complex mountainous terrain as well as the cost and labor intensity of currently available methods. We present a novel approach to infer the processes and dynamics of high-elevation snowmelt contributions predicated upon stable hydrogen and oxygen isotope ratios observed in streamflow. We show that deuterium-excess (d-excess) values of stream water could serve as a comparatively cost-effective proxy for a catchment-integrated signal of high-elevation snowmelt contributions to catchment runoff. We sampled stable hydrogen and oxygen isotope ratios of the precipitation, snowpack, and stream water in the East River, a headwater catchment of the Colorado River, and the stream water of larger catchments at sites on the Gunnison River and Colorado River. The d-excess of snowpack increased with elevation; the upper subalpine and alpine snowpack (> 3200 m) had substantially higher d-excess compared to lower elevations (< 3200 m) in the study area. The d-excess values of stream water reflected this because d-excess values increased as the higher-elevation snowpack contributed more to stream water generation later in the snowmelt/runoff season. End-member mixing analyses based on the d-excess data showed that the share of high-elevation snowmelt contributions within the snowmelt hydrograph was on average 44 % and generally increased during melt period progression, up to 70 %. The observed pattern was consistent during 6 years for the East River, and a similar relation was found for the larger catchments on the Gunnison and Colorado rivers. High-elevation snowpack contributions were found to be higher for years with lower snowpack and warmer spring temperatures. Thus, we conclude that the d-excess of stream water is a viable proxy to observe changes in high-elevation snowmelt contributions in catchments at various scales. Inter-catchment comparisons and temporal trends of the d-excess of stream water could therefore serve as a catchment-integrated measure to monitor if mountain systems rely on high-elevation water inputs more during snow drought compared to years of average snowpack depths.

The stable isotopes of oxygen and hydrogen incorporated in the water molecule (18O and 2H) have become an important tool not only in Isotope Hydrology, routinely applied to study the origin and dynamics of surface and groundwaters, but also in studies related to atmospheric circulation and palaeoclimatic investigations. A proper understanding of the behaviour of these tracers in the water cycle is required for a meaningful use of these tools in any of these disciplines. Our knowledge of the vertical distribution and the factors controlling the stable isotope ratios of oxygen and hydrogen in atmospheric moisture derives from a limited number of observations and vertical profiles in the atmosphere. An international programme jointly operated by the International Atomic Energy Agency (IAEA) and the World Meteorological Organization (WMO), and operational since 1961, has resulted in the development of a dedicated database to monitor isotope ratios in precipitation in more than 500 meteorological stations world-wide. The main features of the spatial and temporal variations of stable isotope ratios of oxygen and hydrogen in precipitation and atmospheric moisture at the global scale are presented based on the analysis of limited data on water vapour, data obtained by the Global Network for Isotopes in Precipitation (GNIP) and the few observations at high latitudes. Copyright © 2000 John Wiley & Sons, Ltd.

The stable isotopes of oxygen and hydrogen incorporated in the water molecule (18O and 2H) have become an important tool not only in Isotope Hydrology, routinely applied to study the origin and dynamics of surface and groundwaters, but also in studies related to atmospheric circulation and palaeoclimatic investigations. A proper understanding of the behaviour of these tracers in the water cycle is required for a meaningful use of these tools in any of these disciplines. Our knowledge of the vertical distribution and the factors controlling the stable isotope ratios of oxygen and hydrogen in atmospheric moisture derives from a limited number of observations and vertical profiles in the atmosphere. An international programme jointly operated by the International Atomic Energy Agency (IAEA) and the World Meteorological Organization (WMO), and operational since 1961, has resulted in the development of a dedicated database to monitor isotope ratios in precipitation in more than 500 meteorological stations world-wide. The main features of the spatial and temporal variations of stable isotope ratios of oxygen and hydrogen in precipitation and atmospheric moisture at the global scale are presented based on the analysis of limited data on water vapour, data obtained by the Global Network for Isotopes in Precipitation (GNIP) and the few observations at high latitudes. Copyright © 2000 John Wiley & Sons, Ltd.

Stable isotopes are commonly utilized for the geographical origin verification of foods, including wheat. However, assessing processed products poses a greater challenge due to the alterations that take place during processing and which have not been fully elucidated yet. In the current study, the effects of the formulation (the mass ratios of gluten to starch), boiling process and their interaction on the stable hydrogen (δ2H) and oxygen (δ18O) isotopic ratios of wheat noodles were evaluated. The δ2H and δ18O of noodles with different formulations (the mass ratios of gluten to starch) as raw materials, in uncooked and cooked (boiled in water) noodles, were examined. The results indicated that the δ2H of the boiled noodles ranged from -80.1‱ to -46.8‱ and were significantly lower than those of the raw materials, which ranged from -73.0‱ to -39.2‱, and the uncooked noodles, which ranged from -73.3‱ to -39.6‱. Oppositely, 18O was enriched in the boiled noodles, ranging from 27.7‱ to 31.3‱, compared with the uncooked noodles, ranging from 28.4‱ to 29.6‱. In addition, a significant interaction effect between the formulation and the boiling process was recorded for δ18O. This study shows that the hydrogen and oxygen stable isotopic compositions of noodles were significantly changed during the boiling process, and the isotopic fractionation varies with the different formulations.