Isotopic composition (δ18O and δD) of precipitation and groundwater in a semi‐arid,mountainous area (Guadiana Menor basin,Southeast Spain)

We characterize the precipitation and groundwater in a mountainous (peaks slightly above 3000 m a.s.l.), semi‐arid river basin in SE Spain in terms of the isotopes ¹⁸O and ²H. This basin, with an extension of about 7000 km², is an ideal site for such a study because fronts from the Atlantic and the Mediterranean converge here. Much of the land is farmed and irrigated both by groundwater and runoff water collected in reservoirs. A total of approximately 100 water samples from precipitation and 300 from groundwater have been analysed. To sample precipitation we set up a network of 39 stations at different altitudes (800–1700 m a.s.l.), with which we were able to collect the rain and snowfall from 29 separate events between July 2005 and April 2007 and take monthly samples during the periods of maximum recharge of the aquifers. To characterize the groundwater we set up a control network of 43 points (23 springs and 20 wells) to sample every 3 months the main aquifers and both the thermal and non‐thermal groundwater. We also sampled two shallow‐water sites (a reservoir and a river). The isotope composition of the precipitation forms a local meteoric water line (LMWL) characterized by the equation δD = 7·72δ¹⁸O + 9·90, with mean values for δ¹⁸O and δD of − 10·28‰ and − 69·33‰, respectively, and 12·9‰ for the d‐excess value. To correlate the isotope composition of the rainfall water with groundwater we calculated the weighted local meteoric water line (WLMWL), characterized by the equation δD = 7·40δ¹⁸O + 7·24, which takes into account the quantity of water precipitated during each event. These values of (dδD/dδ¹⁸O)< 8 and d‐excess (δD–8δ¹⁸O)< 10 in each curve bear witness to the ‘amount effect’, an effect which is more manifest between May and September, when the ground temperature is higher. Other effects noted in the basin were those of altitude and the continental influence. The isotopic compositions of the groundwater are represented by the equation δD = 4·79δ¹⁸O − 18·64. The groundwater is richer in heavy isotopes than the rainfall, with mean values of − 8·48‰ for δ¹⁸O and − 59·27‰ for δD. The isotope enrichment processes detected include a higher rate of evaporation from detrital aquifers than from carbonate ones, the effects of recharging aquifers from irrigation return flow and/or from reservoirs' leakage and enrichment in δ¹⁸O from thermal water. Copyright © 2010 John Wiley & Sons, Ltd.     

Isotopic composition of precipitation in a topographically steep,seasonally snow‐dominated watershed and implications of variations from the global meteoric water line

The local meteoric water line (LMWL), the functional relationship between locally measured values of δ¹⁸O and δ²H in precipitation, represents the isotopic composition of water entering hydrologic systems. The degree to which the LMWL departs from the global meteoric water line (GMWL), moreover, can reveal important information about meteoric sources of water (e.g. oceanic or terrestrial) and atmospheric conditions during transport. Here we characterize the isotopic composition of precipitation within an experimental watershed in the Western US that is subject to large topographic and seasonal gradients in precipitation. Interpreting the hydrometeorologic and spatial controls on precipitation, we constructed a seasonally weighted LMWL for southwestern Idaho that is expressed by the equation δ²H = 7.40 × δ¹⁸O ? 2.17. A seasonally weighted LMWL that is based on weighting isotopic concentrations by climatic precipitation volumes is novel, and we argue better represents the significant seasonality of precipitation in the region. The developed LMWL is considerably influenced by the semiarid climate experienced in southwest Idaho, yielding a slope and y‐intercept lower than the GMWL (δ²H = 8 × δ¹⁸O + 10). Moderate to strong correlations exist between the isotopic composition of precipitation from individual events and surface meteorologic variables, specifically surface air temperature, relative humidity, and precipitation amount. A strong negative correlation exists between the annual average isotopic composition of precipitation and elevation at individual collection sites, with a lapse rate of ?0.22‰/100 m. Copyright © 2016 John Wiley & Sons, Ltd.     

Influence of below-cloud evaporation on stable isotopes of precipitation in the Yellow River source region

The study of below-cloud evaporation effects under clouds in the Yellow River source region is of great significance for regional water resource generation as well as for water resource security in the arid and semi-arid regions of northern China. In this study, we quantitatively assessed the evapotranspiration effect in the Yellow River source region from March to November based on the improved Stewart model. The study concluded that: (1) below-cloud evaporation was slightly higher in summer than in other seasons (residual fractions of raindrop evaporation were 80.57% in summer, 81.12% in spring, and 84.2% in autumn, respectively); and (2) sub-cloud evaporation diminishes with increasing altitude (residual fractions of raindrop evaporation were 83.09% in the western part of the area, 81.82% in the central part of the area, and 81.36% in the eastern part of the area, respectively). (3) The total linear index between study areas f and ∆d is 2.24, where f > 95%, it is 1.19; that is, the evaporation of raindrops increases by 1% and the reduction in the excess of mercury by about 2‰. (4) Local meteorological factors (temperature, precipitation, and relative humidity) and raindrop diameter have a cross-influence on below-cloud evaporation, with relative humidity having the most significant effect, with the highest correlation coefficient of 3.03 when relative humidity is less than 70%. The results of the study can provide a parameter basis for hydrological and climatic models in the Yellow River Basin.     

Using stable water isotopes to identify spatio-temporal controls on groundwater recharge in two contrasting East African aquifer systems

Understanding the spatio-temporal variability in groundwater recharge is a prerequisite to sustainable management of aquifers. Spatial analysis of groundwater stable isotopes uncovered predominant controls on groundwater recharge in the Nairobi aquifer system (NAS) and the South Coast aquifer (SC), two exemplar East African aquifers relied upon by 7 million people. We analysed 368 samples for stable isotopes and basic physico-chemical parameters. The NAS groundwater isotopes are controlled by precipitation orographic effects and enriched recharge from impounded lakes/wetlands; the SC isotopes are correlated with water-table depth influencing evapotranspiration. Global Network of Isotopes in Precipitation (GNIP) data revealed groundwater recharge during months of heavy rains in the NAS, whilst the SC experiences spatio-temporally diffuse recharge. Inferred “isoscapes” show: in the NAS, (1) direct, rapid recharge favoured by faults, well-drained soils and ample rainfall in uplands, (2) delayed recharge from impounded lakes and wetlands in mid-lands, and (3) focused, event-based recharge in floodplains; and in the SC, diffuse recharge complicated by significant water-table evapotranspiration processes.     

Origin and type of rainfall for recharge of a karstic aquifer in the western Mediterranean: a case study from the Sierra de Gador–Campo de Dalias (southeast Spain)

Isotope signatures in precipitation from the Global Network for Isotopes in Precipitation around the Mediterranean basin and literature data are compared with isotopic data from a large karstic aquifer in southeast Spain to explain the origin and type of the precipitation events dominating recharge. Analysis of the deuterium excess d at the scale of the Mediterranean basin and at the regional scale allows us to understand the isotopic context of the study area: Campo de Dalias and the Sierra de Gador (Almería province). The origin of precipitation can be determined from its d value. The d value changes as a function of the initial evaporation condition. It depends on the relative humidity and temperature during the evaporation producing the water vapour of the clouds. The water vapour, which dominates the study area, is generated in two areas: the Atlantic Ocean (d = 10‰) and the western Mediterranean basin (d = 15‰). With increasing precipitation volume, the western Mediterranean character dominates. These heavier storms contribute mainly to recharge, as illustrated by the d value of 13·6‰ in deep groundwater of the Campo de Dalias. Weighted d values increase with the volume of precipitation, giving a significant relationship for the southern and eastern coasts of the Iberian Peninsula. This selectivity of d to monthly precipitation was used to estimate the return period of precipitation leading to aquifer recharge at 0·9–4·9 years. Moderate rainfall, which occurs more frequently, still represents ～60–90% of the total precipitation. One of the challenges to meet ever‐growing water demands is to increase recharge from moderate events yielding intermediate quantities per event, but forming the bulk of the annual precipitation. Copyright © 2006 John Wiley & Sons, Ltd.     

Spatial distribution and seasonal variation in 18O/16O of modern precipitation and river water across the conterminous USA

We report a quantitative analysis of regional differences in the the oxygen isotope composition of river water and precipitation across the USA because data are now available to undertake a more geographically and temporally extensive analysis than was formerly possible. Maps of modern, mean annual δ¹⁸O values for both precipitation (δ¹⁸O_PPT) and river water (δ¹⁸O_RIV) across the 48 contiguous states of the USA have been generated using latitude and elevation as the primary predictors of stable isotope composition while also incorporating regional and local deviations based on available isotopic data. The difference between these two maps was calculated to determine regions where δ¹⁸O_RIV is significantly offset from local δ¹⁸O_PPT. Additional maps depicting seasonal and extreme values for δ¹⁸O_RIV and δ¹⁸O_PPT were also constructed. This exercise confirms the presence of regions characterized by differences in δ¹⁸O_RIV and δ¹⁸O_PPT and specifically identifies the magnitude and regional extent of these offsets. In particular, the Great Plains has δ¹⁸O_RIV values that are more positive than precipitation, while much of the western USA is characterized by significantly lower δ¹⁸O_RIV values in comparison with local δ¹⁸O_PPT. The most salient feature that emerged from this comparison is the ‘catchment effect’ for the rivers. Because river water is largely derived from precipitation that fell upstream of the sample locality (i.e. at higher elevations) δ¹⁸O_RIV values are often lower than local δ¹⁸O_PPT values, particularly in catchments with high‐elevation gradients. Seasonal patterns in the isotopic data substantiate the generally accepted notion that amplitudes of δ¹⁸O variation are greatly dampened in river water relative to those of local precipitation. Copyright © 2005 John Wiley & Sons, Ltd.     

Stable isotopes in the source waters of the Yamuna and its tributaries: seasonal and altitudinal variations and relation to major cations

Water samples from the Yamuna and its tributaries, one of the major river systems draining the Himalaya, have been analysed for their stable oxygen and hydrogen isotopes during three seasons (summer, monsoon and post‐monsoon). The data show clear seasonal and altitudinal variations; waters from higher altitudes and those collected during monsoon season are characterized by relatively depleted isotopic composition. Regression analysis of δD–δ¹⁸O data of samples collected during summer and monsoon seasons shows that the slope of the best‐fit lines are nearly identical to those of precipitation at New Delhi for the same period. The similarity in their slopes suggests that the isotopic composition of precipitation contributing water to these rivers are reasonably well preserved in both monsoon and non‐monsoon seasons, however, during the non‐monsoon period both rainfall and river waters carry signatures of evaporation. The ‘deuterium excess’ in river waters during the three seasons though overlap with each other, the values during October are higher. This can be understood in terms of recycled moisture contributions to precipitation. The ‘altitude effect’ for δ¹⁸O in these waters is determined to be 0·11‰ per 100 m, a factor of about two less than that reported for the Ganga source waters from similar altitudinal range. The variability in altitude effects in rivers draining the Himalaya seems to be controlled by the ‘amount effect’ associated with the monsoon. The significant spatial variability in altitude effect in these river basins, which are a few hundred kilometers apart, suggests that reconstruction of palaeoelevation in the Himalaya, based on δ¹⁸O‐altitude gradients, would depend critically on its proper assessment in the region. This study has established a relationship between total cation abundance and δ¹⁸O in waters of the Yamuna mainstream; total cations (corrected for cyclic components) double for a 1·4 km decrease in altitude as the Yamuna flows downstream. Copyright © 2002 John Wiley & Sons, Ltd.     

Dual effects of precipitation and evaporation on lake water stable isotope composition in the monsoon region

We present the results of a 3‐year monitoring programme of the stable isotope composition of lake water and precipitation at Taozi Lake, in the East Asian monsoon region of China. Our aims were to reveal the spatiotemporal pattern of variation of stable isotopes in a small closed‐basin lake and to quantitatively determine the impacts of precipitation and evaporation on the stable isotope composition of lake water under a humid monsoon climate. In the time domain, the stable oxygen isotopic ratio of the lake water (δ¹⁸O_L) exhibited substantial seasonal and interannual variations, but the isotope variations between different precipitation events substantially exceeded seasonal and interannual variations. Compared with the stable isotopes in precipitation, δ¹⁸O_L was substantially positive and d_L was negative. In the space domains, the lake water was homogeneously mixed. Indicated by statistic analyses, precipitation plays a dominant role in dynamic of the lake stable isotope during precipitation events of relatively large magnitude, whereas the effect of evaporation is dominant during smaller precipitation events. Results advance our understanding of the stable isotope change rule in the process of lake water evaporation, and it is helpful to identify the climatic significance recorded in stable isotopic compositions of lake bottom sediments.     

Identifying the source of atmospheric moisture over arid deserts using stable isotopes (2H and 18O) in precipitation

Precipitation is a major component of the hydrologic cycle in arid desert areas. To date, however, few studies have been conducted on investigating the isotope characteristics and moisture sources of precipitation in arid desert environments. The Alxa Desert Plateau is a critical arid desert area in North China. This study is the first to analyse the stable isotopic composition of precipitation to identify the sources of atmospheric moisture over this plateau. Our results show that the δD and δ¹⁸O values of precipitation across the plateau change greatly at both daily and monthly timescales, and exhibit seasonal variations. Among the main meteorological parameters, atmospheric temperature is the most predominant factor controlling the isotopic composition and the δD–δ¹⁸O relationship of local precipitation. Analyses of the precipitation isotopes with the Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) model reveal that (a) the westerly and polar moisture sources are the dominant controls on summer and winter precipitation and (b) the evaporation of local lake water significantly affects winter precipitation even though it only represents a small amount. Based on the isotope data of 2013–2016 precipitation, a local meteoric water line (LMWL) is derived: δD = (8.20 ± 0.22)·δ¹⁸O + (8.15 ± 2.16)‰ for the study site. Compared to the global meteoric water line, the LMWL has a greater slope and lower d‐excess. This can be explained by admixing of atmospheric moisture resulting from the evaporation of local lake water. Based on this LMWL, we are able to trace that groundwater of the Badain Jaran Desert originates from the surrounding mountains with altitudes of <4,000 m. The newly derived LMWL shows that the recharge altitudes of desert groundwater are overestimated on the basis of the previous LMWLs. This study not only provides insights into the hydrological cycle but also offers guidance for water resource management in arid desert areas of China. Additionally, this study provides techniques that can be applied to the analyses of precipitation isotopes in similar arid regions of the world.     

A study on the spatial variations in stable isotopic composition of precipitation in a semiarid region of Southern India

The stable isotope analysis of all major rain events from Moinabad (MB), Rajendranagar (RN) and Osmanasagar (OS) reservoir, three closely placed locations in Hyderabad, India, were carried out during the 2005 to 2008 period. The OS station recorded the highest amount of rainfall with an average value of 1000 mm, whereas the MB station recorded the lowest average rainfall of 790 mm. The stable isotope (δ¹⁸O) values of the precipitation samples during these period varied from ?11.43‰ to ?0.03‰ for the MB station, ?8.21‰ to 0.54‰ for the RN station and ?11.47‰ to 0.72‰ for the OS station. The d‐excess of precipitation at the three stations also showed considerable variations and revealed that the precipitation in the region undergoes significant modification through secondary evaporation during its fall. The possible causes for these observed spatial and temporal variations in amount and the isotopic composition of precipitation in a small geographical area within the city were studied. The observed variations may be attributed to the regional scale differences in water budget induced by rapid urbanisation activities in the city coupled with the differences in secondary effects undergone by the falling drops. This study elucidating changes in precipitation patterns in the city and its possible causes may largely help in its water balance calculation. Copyright © 2011 John Wiley & Sons, Ltd.     

Spatial variation of isotope composition in precipitation in a tropical environment: a case study from the Deduru Oya river basin,Sri Lanka

The stable isotope composition (¹⁸O and ²H) in the tropical precipitation collected from 18 locations throughout the Deduru Oya river basin in Sri Lanka, has been studied during August and September 2001, in order to characterize the isotopic composition of precipitation in the dry and intermediate climatic zones of Sri Lanka. The isotope compositions are described with respect to the distance from the coast and the altitude. The analyses show that δ¹⁸O vary from ? 5·11 to 1·39‰ and δD vary from ? 35·71 to 12·55‰. The d‐excess values range from ? 0·65 to 13·17 with an average value of ～7. Regression for the δ¹⁸O ? δD is y = 6·8x + 4·9 (R² = 0·9) which is compatible with the precipitation in other tropical regions. The lower slope in the regression line and the lower d‐excess value indicate high temperature events which were possibly aided by concentration through successive evaporation within the atmosphere. The spatial variation of isotope composition indicates two different cloud contributions for the rain events, of which one may be linked to the Indian Ocean contribution and the other to the high altitude condensation. Copyright © 2008 John Wiley & Sons, Ltd.     

Using stable isotopes 18O and 2H of lake water and biogeochemical analysis to identify factors affecting water quality in four estuarine Amazonian shallow lakes

Stable isotopes analyses of oxygen and hydrogen of lake water were used to estimate the effect of evaporation (E) on the water quality of four shallow lakes in the Amapá State coast—Amazon/Brazil. These lakes, with different size and hydrologic conditions, were sampled during the course of the 2015/2016 El‐Niño (record‐breaking warming/drought in the Amazon rainforest). Hydrometeorological and water quality parameters were simultaneously performed to the isotopic sampling. The results showed that the evaporation process and the water quality can be explained by climate season and distances from the Atlantic Ocean. Lake evaporation losses ranged from ≈0–22% during the wet season in April/2016 and ≈35.7% during the dry season in November/2015. As expected, the evaporation of lake water was greater during the dry season, but it was higher for lakes farther away from the Atlantic Ocean compared with more coastal lakes due to tidal preponderance and the influence of major river channels. The more inland estuarine lakes showed a lower level of salinity (0.00–0.03 ppt) compared with those closer to the Atlantic Ocean (0.01–0.08 ppt). The El Niño phenomenon, with a lower precipitation in the Amazon basin, may initiate salinization of lakes closer to the Atlantic Ocean. Furthermore, strong mean seasonal variations of evaporation (0.06 ≤ E ≤ 0.22) and other hydrologic parameters were observed (precipitation, water temperature, and water depth), with significant effects on the water quality such as salinity, dissolved oxygen, chlorophyll (p < .05). We conclude that the occurrence of the extreme climatic events can disrupt the biogeochemical and hydrological balance of these aquatic ecosystems and salinization of lakes closer to the Atlantic Ocean.     

Spatial and temporal distributions of stable isotopes in precipitation over Thailand

Spatial and temporal variations of the isotopic composition of precipitation over Thailand were investigated. The local meteoric water line for Thailand deviates slightly from the global meteoric water line, with lower slopes (7.62 ± 0.07, 7.59 ± 0.08) and intercepts (6.42 ± 0.39, 6.22 ± 0.42) using ordinary and precipitation weighted methods. Differences in spatial and temporal δ¹⁸O distributions between the tropical monsoon and tropical savanna climate zones were found due to differing moisture source contributions and seasonal precipitation patterns. The temporal data reveals that the northeast monsoon rains originate from isotopically-enriched local moisture with isotope values of −9.36 to −0.09‰ (mean − 3.73 ± 0.42‰), whereas the southwest monsoon clouds had a more significant rainout effect from Rayleigh distillation, with isotope values of −9.56 to −1.78‰ (mean − 5.40 ± 0.38‰). The precipitation amount at each site was negatively correlated with δ¹⁸O (−0.24 to −3.20‰ per 100 mm, R² = 0.1–0.9). Furthermore, δ¹⁸O was negatively correlated with geography (latitude, altitude) for the southwest monsoon periods, as expected based on other observed correlations. However, an inverse correlation was seen in the northeast monsoon due to differing moisture transportation as part of the continental effect. The correlation coefficient (R) was higher in the southwest monsoon (−0.84 for latitude effect, −0.64 for altitude effect) than the northeast monsoon (0.67 for latitude effect, 0.35 for altitude effect). The spatial pattern of isotopic composition reflects the southwest monsoon more clearly than the northeast monsoon, but the two monsoons also have a cancelling impact on orographic patterns. An agreement of the δ¹⁸O and deuterium excess (d-excess) was a negative correlation and found to reflect precipitation sources and re-evaporation processes. The d-excess was slightly higher for the northeast monsoon, bringing moisture from the Pacific Ocean and travelling across the continent before reaching the observed stations. By contrast, the d-excess was relatively lower for the Indian Ocean's moisture in the southwest monsoon.     

The stable isotopes of natural waters at the Marcell Experimental Forest

We present a new data set from the Marcell Experimental Forest (MEF) that compiles water isotope measurements from multiple research catchments, some of which have been studied since the 1960s. The MEF is located in northern Minnesota, USA, and is home to heavily studied and monitored forests, streams, bogs, and fens. Peat-forming systems (bogs and fens) are an important component of the MEF landscape and have a profound impact on the water cycle in these catchments. Within the last decade, analysis of stable isotopes of water (expressed as δD and δ¹⁸O) has been implemented to characterize the different components of the water budget, and to allow researchers to look at catchment and peatland-specific hydrologic effects in the watershed. This δD and δ¹⁸O data set of natural waters from MEF catchments is primarily composed of measurements from three peatlands (S1, S2, S6) during an 11-year period. More recently collection and analysis were expanded to also include samples from the Spruce and Peatland Responses Under Changing Environments (SPRUCE) project in the S1 bog, peatlands S3, S4, S5, as well as nearby lakes. We establish a local meteoric water line by analyzing the isotopic composition of precipitation, which fills a void in regional meteoric water lines for Minnesota. Furthermore, we establish baseline isotopic composition for bog outlet streams, bog porewater, aquifer groundwater, overland flow, subsurface stormflow, and snowpack, as well as runoff from the SPRUCE experimental chambers. These data are publicly available and will be expanded upon in the future.     

Spatial and temporal variations of stable isotopes in precipitation in midlatitude coastal regions

Spatial and temporal variations of the isotopic composition of precipitation were investigated to better understand their controlling factors. Precipitation was collected from six locations in Hokkaido, Japan, and event‐based analyses were conducted for a period from March 2010 to February 2013. Relatively low δ values and a high d‐excess for annual averages were observed at three sites located along the Japan Sea compared to the three sites at Pacific Ocean side. Lower δ values in spring and fall and higher d‐excess in winter were observed for the region along the Japan Sea. In total, 264 precipitation events were identified. Precipitation originated predominantly from low‐pressure system (LPS) events, which were classified as northwest (LPS‐NW) and southeast (LPS‐SE) events according to the routes of the low‐pressure center, that passed northwest and southeast of Hokkaido, respectively. LPS‐SE events showed lower δ¹⁸O than LPS‐NW events, which is attributable to the lower δ¹⁸O of water vapor resulting from heavy rainfalls in the upstream region of the LPS air mass trajectories over the Pacific Ocean. This phenomenon observed in Hokkaido can be found in other midlatitude coastal regions and applied for hydrological, atmospheric, and paleoclimate studies. A characteristic spatial pattern was found in LPS‐NW events, in which lower δ¹⁸O was observed on the Japan Sea side than on the Pacific Ocean side in each season. This is likely due to the location of the sampling sites and their distance from the LPS: Precipitation with lower δ¹⁸O in the region along the Japan Sea occurs in a well‐developed cloud system near the low‐pressure center in cold and warm sectors of LPS, whereas precipitation with higher δ¹⁸O on the Pacific side mainly occurs in a warm sector away from the low‐pressure center. Air mass from the north does not always cause low δ in precipitation, and the precipitation process in the upstream region is another important factor controlling the isotopic composition of precipitation, other than the local temperature and precipitation amount.     

Seasonal variations of deuterium and oxygen‐18 isotopes and their response to moisture source for precipitation events in the subtropical monsoon region

Deuterium and oxygen‐18 are common environmental tracers in water used to investigate hydrological processes such as evaporation and groundwater recharge, and to trace moisture source. In this study, we collected event precipitation from 01 January 2010 to 28 February 2011 at a site in Changsha, Yangtze River Basin to estimate the influence of moisture source and atmospheric conditions on stable isotope compositions. The local meteoric water line, established as δD = (8.45 ± 0.13) δ¹⁸O + (17.7 ± 0.9) (r² = 0.97, n = 189), had a higher slope and intercept than global meteoric water line. Temperature–δ¹⁸O exhibited complex correlations, with positive correlations during Nov.–Apr. superior to during Jun.–Sep., which was attributed to distinctive moisture sources, but vague the overall period; amount effect examined throughout the year. Linear regressions between δ¹⁸O and δD value in different precipitation event size classes revealed progressively decreasing slope and intercept values with decreasing precipitation amount and increasing vapour pressure deficit, indicating that small rainfall events (0–5 mm) were subject to secondary evaporation effects during rainwater descent. In contrast, snowfall and heavy precipitation events exhibited high slope and intercepts for the regression equation between δ¹⁸O and δD. High concentrations of heavy isotopes were associated with precipitation events sourced from remote westerly air masses, degenerated tropical marine air masses from the Bay of Bengal (BoB), and inland moisture in the pre‐monsoon period, as determined from backward trajectories assessed in the HYSPLIT model. Meanwhile, low concentrations of heavy isotopes were found to correspond with remote maritime moisture from BoB, the South China Sea, and the west Pacific at three different air pressures in summer monsoon and post‐monsoon using HYSPLIT and records of typhoon paths. These findings suggest that stable isotope compositions in precipitation events are closely associated with the meteorological conditions and respond sensitively to moisture source in subtropical monsoon climates. Copyright © 2013 John Wiley & Sons, Ltd.     

Spatial and temporal variability of stable isotopes (δ18O and δ2H) in surface waters of arid,mountainous Central Asia

Characterization of spatial and temporal variability of stable isotopes (δ¹⁸O and δ²H) of surface waters is essential to interpret hydrological processes and establish modern isotope–elevation gradients across mountainous terrains. Here, we present stable isotope data for river waters across Kyrgyzstan. River water isotopes exhibit substantial spatial heterogeneity among different watersheds in Kyrgyzstan. Higher river water isotope values were found mainly in the Issyk‐Kul Lake watershed, whereas waters in the Son‐Kul Lake watershed display lower values. Results show a close δ¹⁸O–δ²H relation between river water and the local meteoric water line, implying that river water experiences little evaporative enrichment. River water from the high‐elevation regions (e.g., Naryn and Son‐Kul Lake watershed) had the most negative isotope values, implying that river water is dominated by snowmelt. Higher deuterium excess (average d = 13.9‰) in river water probably represents the isotopic signature of combined contributions from direct precipitation and glacier melt in stream discharge across Kyrgyzstan. A significant relationship between river water δ¹⁸O and elevation was observed with a vertical lapse rate of 0.13‰/100 m. These findings provide crucial information about hydrological processes across Kyrgyzstan and contribute to a better understanding of the paleoclimate/elevation reconstruction of this region.     

Orographic distillation and spatio‐temporal variations of stable isotopes in precipitation in the North Atlantic

Little is known about the spatial and temporal variability of the stable isotopic composition of precipitation in the North Atlantic and its relationship to the North Atlantic Oscillation (NAO) and anthropogenic climate change. The islands of the Azores archipelago are uniquely positioned in the middle of the North Atlantic Ocean to address this knowledge gap. A survey of spatial and temporal variability of the stable isotope composition of precipitation in Azores is discussed using newly presented analyses along with Global Network of Isotopes in Precipitation data. The collected precipitation samples yield a new local meteoric water line (δ²H = 7.1 * δ¹⁸O + 8.46) for the Azores region and the North Atlantic Ocean. The annual isotopic mean of precipitation shows a small range for the unweighted and precipitation mass‐weighted δ¹⁸O‐H₂O values. Results show an inverse relation between the monthly δ¹⁸O‐H₂O and the amount of precipitation, which increases in elevation and into the interior of the island. Higher amounts of precipitation (from convective storm systems) do not correspond to the most depleted values of stable isotopes in precipitation. Precipitation shows an orographic effect with depleted δ¹⁸O‐H₂O values related to the Rayleigh effect. Monthly δ¹⁸O‐H₂O values for individual precipitation sampling stations show little relationship to air temperature. Results show a local source of moisture during the summer with the characteristics of the first vapour condensate. The stable isotope composition of precipitation is strongly correlated to the NAO index, and δ¹⁸O‐H₂O values show a statistically significantly trend towards enrichment since 1962 coincident with the increased air temperature and relative humidity due to climate change. Results are in line with observations of increasing sea surface temperature and relative humidity.     

Mechanisms of isotopic control of precipitation in the Yellow River source region

The study of water vapour sources and water cycle patterns in the Yellow River source region is of great significance for ensuring water resource security in the arid and semi-arid regions of northern China. We established a precipitation stable isotope observation system in the Yellow River source region for three consecutive years (2020–2022), systematically analysed the spatial and temporal distribution characteristics of precipitation stable isotopes ²H and ¹⁸O in the Yellow River source region and their interrelationships with environmental factors and topography, and explored the regional water vapour transport pathways by using the HYSPLIT model and combining with the global reanalysis data. The results show that: (1) the δ¹⁸O and δ²H values of precipitation in the Yellow River source region follow the seasonal pattern, with the first half of the year being richer than the second half of the year; (2) the spatial variations of δ¹⁸O of precipitation in the Yellow River source region show a low in the southwest and a high in the northeast; (3) the water vapour source in the source area is basically stable, and the complex transport paths and the cross-effects of the local factors determine the stable isotope characteristics of the water, and the stable isotope characteristics of the water are determined by the cross-effects of the local factors, because the source of the water vapour and the local factors such as the height will not change significantly in the short term. Since the source of water vapour and local elevation factors will not change significantly in the short term, the precipitation pattern in the source area of the Yellow River can be considered to be basically stable.     

Use of stable isotopes to understand run‐off generation processes in the Red River Delta

This paper presents the use of stable isotopes of water for hydrological characterization and flow component partitioning in the Red River Delta (RRD), the downstream section of the Red River. Water samples were collected monthly during 2015 from the mainstream section of the river and its right bank tributaries flowing through the RRD. In general, δ¹⁸O and δ²H river signatures were depleted in summer–autumn (May–October) and elevated in winter–spring (November–April), displaying seasonal variation in response to regional monsoon air mass contest. The Pacific equatorial–maritime air mass dominates in summer and the northern Asia continental air mass controls in winter. Results show that water of the RRD tributaries stems solely from local sources and is completely separated from water arriving from upstream subbasins. This separation is due to the extensive management of the RRD (e.g., dykes and dams) for the purposes of irrigation and inundation prevention. Mainstream river section δ¹⁸O and δ²H compositions range from ?10.58 and ?73.74‰ to ?6.80 and ?43.40‰, respectively, and the corresponding ranges inside the RRD were from ?9.35 and ?64.27‰ to ?2.09 and ?15.80‰. A combination of data analysis and hydrological simulation confirms the role of upstream hydropower reservoirs in retaining and mixing upstream water. River water inside the RRD experienced strong evaporation characterized by depleted d‐excess values, becoming negative in summer. On the other hand, the main stream of the Red River has d‐excess values around 10‰, indicating moderate evaporation. Hydrograph separation shows that in upstream subbasins, the groundwater fraction dominates the river flow composition, especially during low flow regimes. Inside the RRD, the river receives groundwater during the dry season, whereas groundwater replenishment occurs in the rainy season. Annual evaporation obtained from this hydrograph separation computation was about 6.3% of catchment discharge, the same order as deduced from the difference between subbasin precipitation and discharge values. This study shows the necessity to re‐evaluate empirical approaches in large river hydrology assessment schemes, especially in the context of climate change.