Distribution of tritium and stable isotopes in precipitation in Syria

Abstract

The paper discusses aspects of the isotopic composition (tritium and stable isotopes) of precipitation, which was monitored from 2000 to 2003 at 12 stations in Syria. The seasonal variations in δ¹⁸O are smaller at the western stations than at the eastern ones due to low seasonal temperature variations. A good correlation between δ²H and δ¹⁸O was obtained for each station, and the slopes of the local meteoric water lines are significantly lower than the Global Meteoric Water Line. Values of d-excess decrease from 19‰ at the western stations to 13‰ at the eastern ones, indicating the influence of precipitation generated by air masses coming from the Mediterranean Sea. A reliable altitude effect represented by depletion of heavy stable isotopes (δ¹⁸O and δ²H), of about??0.21‰ and??1.47‰ per 100 m elevation, respectively, was observed. Monthly tritium contents in precipitation, and seasonal variations, are less at the western stations than at the eastern ones. The weighted mean tritium values are between 3 and 9 TU, and increase with distance from the Syrian coast by 1 TU/100 km.

Citation Al Charideh, A. R. & Abou Zakhem, B. (2010) Distribution of tritium and stable isotopes in precipitation in Syria. Hydrol. Sci. J. 55(5), 832–843.     

Chloride,hydrochemical and isotope methods of groundwater recharge estimation in eastern Mediterranean areas: a case study in Jordan

Jordan is classified as an arid to semi‐arid country with a population according to 1999 estimates of 4·8 millions inhabitants and a growth rate of 3·4%. Efficient use of Jordan's scarce water is becoming increasingly important as the urban population grows. This study was carried out within the framework of the joint European Research project ‘Groundwater recharge in the eastern Mediterranean’ and describes a combined methodology for groundwater recharge estimation in Jordan, the chloride method, as well as isotopic and hydrochemical approaches. Recharge estimations using the chloride method range from 14 mm year^?1 (mean annual precipitation of 500 mm) for a shallow and stony soil to values of 3·7 mm year^?1 for a thick desert soil (mean annual precipitation of 100 mm) and values of well below 1 mm year^?1 for thick alluvial deposits (mean annual rainfall of 250 mm). Isotopically, most of the groundwater in the Hammad basin, east Jordan, falls below the global meteoric water line and far away from the Mediterranean meteoric water line, suggesting that the waters are ancient and were recharged in a climate different than Mediterranean. Tritium levels in the groundwater of the Hammad basin are less than the detection limit (<1·3 TU). However, three samples in east Hammad, where the aquifer is unconfined, present tritium values between 1 and 4 TU. Copyright © 2007 John Wiley & Sons, Ltd.     

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.     

Short‐term variability in isotopic composition of precipitation: A case study from the Midwestern United States

Oxygen and deuterium isotopes in precipitation were analysed to define local isotopic trends in Iowa, US. The area is far inland from an oceanic source and the observed averages of δ¹⁸O and δ D are ? 6·43‰ and ? 41·35‰ for Ames, ? 7·53‰ and ? 51·33‰ for Cedar Falls, and ? 6·01‰ and ? 38·19‰ for Iowa City, respectively. Although these data generally follow global trends, they are different when compared to a semi‐arid mid‐continental location in North Platt, Nebraska. The local meteoric water lines of Iowa are δ D = 7·68 δ¹⁸O + 8·0 for Ames, δ D = 7·62 δ¹⁸O + 6·07 for Cedar Falls, and δ D = 7·78 δ¹⁸O + 8·61 for Iowa City. The current Iowa study compares well with a study conducted in Ames, Iowa, 10 years earlier. The differences between Iowa and Nebraska studies are attributed to a variable climate across the northern Great Plains ranging from sub‐humid in the east to semi‐arid in the west. Iowa being further east in the region is more strongly influenced by a moist sub‐humid to humid climate fed by the tropical air stream from the Gulf of Mexico. The average d‐excess values are 10·06‰ for Ames, 8·92‰ for Cedar Falls and 9·92‰ for Iowa City. Eighty seven percent of the samples are within the global d‐excess range of 0‰ and 20‰. The results are similar to previous studies, including those by National Atmospheric Deposition Programs and International Atomic Energy Agency. It appears that the impact of recycled water or secondary evaporation on δ¹⁸O values of area precipitation is minimal. Copyright © 2008 John Wiley & Sons, Ltd.     

Stable isotopic characteristic of Taiwan's precipitation: A case study of western Pacific monsoon region

The stable oxygen and hydrogen isotopic features of precipitation in Taiwan, an island located at the western Pacific monsoon area, are presented from nearly 3,500 samples collected during the past decade for 20 stations. Results demonstrate that moisture sources from diverse air masses with different isotopic signals are the main parameter in controlling the precipitation's isotope characteristics. The air mass from polar continental (Pc) region contributes the precipitation with high deuterium excess values (up to 23‰) and relatively enriched isotope compositions (e.g., ? 3.2‰ for δ¹⁸O) during the winter with prevailing northeasterly monsoon. By contrast, air masses from equatorial maritime (Em) and tropical maritime (Tm) supply the precipitation with low deuterium excess values (as low as about 7‰) and more depleted isotope values (e.g., ? 8.9‰ and ? 6.0‰ for δ¹⁸O of Tm and Em, respectively) during the summer with prevailing southwesterly monsoon. Thus seasonal differences in terms of δ¹⁸O, δD, and deuterium excess values are primarily influenced by the interactions among various precipitation sources. While these various air masses travel through Taiwan, secondary evaporation effects further modify the isotope characteristics of the inland precipitation, such as raindrop evaporation (reduces the deuterium excess of winter precipitation) and moisture recycling (increases the deuterium excess of summer precipitation). The semi-quantitative estimations in terms of evaluation for changes in the deuterium excess suggest that the raindrop evaporation fractions for winter precipitation range 7% to 15% and the proportions of recycling moisture in summer precipitation are less than 5%. Additionally, the isotopic altitude gradient in terms of δ¹⁸O for summer precipitation is ? 0.22‰/100 m, greater than ? 0.17‰/100 m of winter precipitation. The greater isotopic gradient in summer can be attributed to a higher temperature vs. altitude gradient relative to winter. The observed spatial and seasonal stable isotopic characteristics in Taiwan's precipitation not only contribute valuable information for regional monsoon research crossing the continent–ocean interface of East Asia, but also can serve as very useful database for local water resources management.     

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.     

Using stable isotopes to determine the water sources in alpine ecosystems on the east Qinghai‐Tibet plateau,China

To investigate the water circulation of eastern Qinghai‐Tibet plateau during rainy season, water samples of precipitation, throughfall, fog, soil, litter and xylem were collected for stable isotope analysis. The results showed that precipitation mainly originated as a result of the East Asian Monsoon, and the secondarily evaporated water from subalpine ecosystem was an important part in local atmospheric water cycle. The deuterium excess of rainfall in the alpine meadow was evidently higher than the precipitation in the Dengsheng stations. This suggests that a large part of precipitation in alpine meadow was derived from secondarily evaporated water and the mean contribution was 39·57%, about 3·65 mm produced shortly after rain events. Through the contrast of delta (d)‐excess value in different water samples, it could be concluded that the water in subalpine shrubland and transpiration of subalpine dark coniferous forest were the main source of secondarily evaporated water that transferred to alpine meadow. Hence, the precipitation on the east Qinghai‐Tibet plateau was doubly controlled by monsoon and local water circulation in alpine ecosystems. Copyright © 2010 John Wiley & Sons, Ltd.     

Geosecs North Atlantic radiocarbon and tritium results

Radiocarbon data for 11 stations and tritium data for 16 stations in the North Atlantic Ocean from 74°N to 3°N are presented. For radiocarbon, normal errors inΔ¹⁴C are± 4‰, and in tritium,± 0.09TU or± 3%, whichever is larger. There is a remarkable, but not simply linear, correlation between oceanic bomb transients in¹⁴C and³H. The deep convective mixing in the Greenland Sea is reflected in substantial bomb tracer penetration to all depths, with residence time for the deep, cold core water that seems to be 20 to 30 years. The outflow in the bottom layer southward over the sills of the Denmark Strait and Faroe Passage carries significant tritium concentration, at least to 40°N. Complicated, but coherent, profile structures in the subtropical Atlantic suggest effects of large-scale lateral advection. In particular, a pronounced minimum in both¹⁴C and³H might be associated with the Antarctic intermediate water.     

Tritium in the Arctic Ocean and East Greenland Current

High concentrations of tritium are found in the surface water of the Arctic Ocean (up to 50 TU) and in the East Greenland Current (up to 70 TU). These high tritium values are a direct result of atmospheric testing of nuclear weapons in the early 1960's. A box model with a time-dependent input of highly tritiated precipitation predicts that high tritium concentrations are to be expected in the surface layer of the Arctic Ocean and its various outflows. We suggest that a few tritium stations in the Arctic Ocean would provide a powerful analytical tool for assigning time scales to exchange processes.     

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.     

Water isotopic variability in Mallorca: a path to understanding past changes in hydroclimate

This paper reports the first results on δ¹⁸O and δ²H analysis of precipitations, cave drip waters, and groundwaters from sites in Mallorca (Balearic Islands, western Mediterranean), a key region for paleoclimate studies. Understanding the isotopic variability and the sources of moisture in modern climate systems is required to develop speleothem isotope‐based climate reconstructions. The stable isotopic composition of precipitation was analysed in samples collected between March 2012 and March 2013. The values are in the range reported by GNIP Palma station. Based on these results, the local meteoric water line (LMWL) δ²H = 7.9 (±0.3) δ¹⁸O + 10.8 (±2.5) was derived, with slightly lower slope than Global Meteoric Water Line. The results help tracking two main sources of air masses affecting the study sites: rain events with the highest δ¹⁸O values (> ?5‰) originate over the Mediterranean Sea, whereas the more depleted samples (< ?8‰) are sourced in the North Atlantic region. The back trajectory analysis and deuterium excess values, ranging from 0.4 to 18.4‰, further support our findings. To assess the isotopic variation across the island, water samples from eight caves were collected. The δ¹⁸O values range between ?6.9 and ?1.6‰. With one exception (Artà), the isotopic composition of waters in caves located along the coast (Drac, Vallgornera, Cala Varques, Tancada, and Son Sant Martí) indicates Mediterranean‐sourced moisture masses. By contrast, the drip water δ¹⁸O values for inland caves (Campanet, ses Rates Pinyades) or developed under a thick (>50 m) limestone cap (Artà) exhibit more negative values. A well‐homogenized aquifer supplied by rainwaters of both origins is clearly indicated by groundwater δ¹⁸O values, which show to be within 2.4‰ of the unweighted arithmetic mean of ?7.4‰. Although limited, the isotopic data presented here constitute the baseline for future studies using speleothem δ¹⁸O records for western Mediterranean paleoclimate reconstructions. Copyright © 2016 John Wiley & Sons, Ltd.     

Estimating the criterion for determining water vapour sources of summer precipitation on the northern Tibetan Plateau

According to the precipitation and δ¹⁸O data obtained during the GEWEX Asian Monsoon Experiment–Tibet Intensive Observation Period, based on the knowledge that δ¹⁸O is lower in precipitation formed from ocean air mass vapour than that from local evaporation vapour, the water vapour sources can be identified from the δ¹⁸O values in precipitation. We attempt to give the identification criterion of δ¹⁸O values in precipitation. The threshold values chosen to distinguish between ocean and local sources are δ¹⁸O < ?20‰ and δ¹⁸O > ?13‰ respectively. According to this criterion, the proportion of local evaporation‐formed precipitation and ocean air‐mass‐formed precipitation in total precipitation was estimated. The average value of precipitation at three sites (NODA, Amdo and AQB) is 249·76 mm. Among this, precipitation formed directly by the ocean air mass vapour is 80·08 mm at most. Precipitation formed by water vapour evaporated from local places is 117·05 mm at least. That is to say that precipitation formed directly by the ocean air mass vapour accounts for 32·06% of the total precipitation at most. Precipitation formed by water vapour evaporated from local places accounts for 46·86% of the total precipitation at least. At least 21·8% of the total precipitation came from water vapour that was evaporated on the way and transported by the monsoon circulation. Copyright © 2005 John Wiley & Sons, Ltd.     

Estimation of mean residence times of subsurface waters using seasonal variation in deuterium excess in a small headwater catchment in Japan

We measured deuterium excess (d = δD ? 8δ¹⁸O) in throughfall, groundwater, soil water, spring water, and stream water for 3 years in a small headwater catchment (Matsuzawa, 0·68 ha) in the Kiryu Experimental Watershed in Japan. The d value represents a kinetic effect produced when water evaporates. The d value of the throughfall showed a sinusoidal change (amplitude: 6·9‰ relative to Vienna standard mean ocean water (V‐SMOW)) derived from seasonal changes in the source of water vapour. The amplitude of this sinusoidal change was attenuated to 1·3–6·9‰ V‐SMOW in soil water, groundwater, spring water, and stream water. It is thought that these attenuations derive from hydrodynamic transport processes in the subsurface and mixing processes at an outflow point (stream or spring) or a well. The mean residence time (MRT) of water was estimated from d value variations using an exponential‐piston flow model and a dispersion model. MRTs for soil water were 0–5 months and were not necessarily proportional to the depth. This may imply the existence of bypass flow in the soil. Groundwater in the hillslope zone had short residence times, similar to those of the soil water. For groundwater in the saturated zone near the spring outflow point, the MRTs differed between shallow and deeper groundwater; shallow groundwater had a shorter residence time (5–8 months) than deeper groundwater (more than 9 months). The MRT of stream water (8–9 months) was between that of shallow groundwater near the spring and deeper groundwater near the spring. The seasonal variation in the d value of precipitation arises from changes in isotopic water vapour composition associated with seasonal activity of the Asian monsoon mechanism. The d value is probably an effective tracer for estimating the MRT of subsurface water not only in Japan, but also in other East Asian countries influenced by the Asian monsoon. Copyright © 2006 John Wiley & Sons, Ltd.     

From precipitation to runoff: stable isotopic fractionation effect of glacier melting on a catchment scale

Stable isotope variability and fractionation associated with transformation of precipitation/accumulation to firn to glacial river water is critical in a variety of climatic, hydrological and paleoenvironmental studies. This paper documents the modification of stable isotopes in water from precipitation to glacier runoff in an alpine catchment located in the central Tibetan Plateau. Isotopic changes are observed by sampling firnpack profiles, glacier surface snow/ice, meltwater on the glacier surface and catchment river water at different times during a melt season. Results show the isotopic fractionation effects associated with glacier melt processes. The slope of the δD‐δ¹⁸O regression line and the deuterium excess values decreased from the initial precipitation to the melt‐impacted firnpack (slope from 9.3 to 8.5 and average d‐excess from 13.4‰ to 7.4‰). The slope of the δD‐δ¹⁸O line further decreased to 7.6 for the glacier runoff water. The glacier surface snow/ice from different locations, which produces the main runoff, had the same δD‐δ¹⁸O line slope but lower deuterium excess (by 3.9‰) compared to values observed in the firnpack profile during the melt season. The δD‐δ¹⁸O regression line for the river water exhibited a lower slope compared to the surface snow/ice samples, although they were closely located on the δD‐δ¹⁸O plot. Isotope values for the river and glacier surface meltwater showed little scatter around the δD‐δ¹⁸O regression line, although the samples were from different glaciers and were collected on different days. Results indicate a high consistency of isotopic fractionation in the δD‐δ¹⁸O relationships, as well as a general consistency and temporal covariation of meltwater isotope values at the catchment scale. Copyright © 2013 John Wiley & Sons, Ltd.     

Future use of tritium in mapping pre-bomb groundwater volumes

The tritium input to groundwater, represented as volume-weighted mean tritium concentrations in precipitation, has been close to constant in Tucson and Albuquerque since 1992, and the decrease in tritium concentrations at the tail end of the bomb tritium pulse has ceased. To determine the future usefulness of tritium measurements in southwestern North America, volume-weighted mean tritium levels in seasonal aggregate precipitation samples have been gathered from 26 sites. The averages range from 2 to 9 tritium units (TU). Tritium concentrations increase with site latitude, and possibly with distance from the coast and with site altitude, reflecting local ratios of combination of low-tritium moisture advected from the oceans with high-tritium moisture originating near the tropopause. Tritium used alone as a tool for mapping aquifer volumes containing only pre-bomb recharge to groundwater will become ambiguous when the tritium in precipitation at the end of the bomb tritium pulse decays to levels close to the analytical detection limit. At such a time, tritium in precipitation from the last one to two decades of the bomb pulse will become indistinguishable from pre-bomb recharge. The threshold of ambiguity has already arrived in coastal areas with a mean of 2 TU in precipitation and will follow in the next three decades throughout the study region. Where the mean tritium level is near 5 TU, the threshold will occur between 2025 and 2030, given a detection limit of 0.6 TU. Similar thresholds of ambiguity, with different local timing possible, apply globally.     

Extreme short‐term stable isotope variability revealed by continuous rainwater analysis

The continuous real‐time analysis, at 30‐s intervals, of precipitation at an Australian tropical location revealed extreme and rapidly changing δ¹⁸O and δD values related to variations in moisture source areas, transport paths and precipitation histories. The range of δ¹⁸O (?19.6‰ to +2.6‰) and δD (?140‰ to +13‰) values from 5948 measurements of nine rain events over 15 days during an 8‐month period at a single location was comparable with the range measured in 1532 monthly samples from all seven Australian Global Network of Isotopes in Precipitation stations from 1962 to 2002. Extreme variations in δ¹⁸O (?8.7‰ to ?19.6‰) and δD (?54‰ to ?140‰) were recorded within a single 4‐h period. Real‐time stable isotope monitoring of precipitation at a high temporal resolution enables new and powerful tracer applications in climatology, hydrology, ecophysiology and palaeoclimatology. Copyright © 2012 John Wiley & Sons, Ltd.     

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.     

Contribution of storms to groundwater recharge in the semi‐arid region of Karnataka,India

This paper describes the application of environmental isotopes and injected tracer techniques in estimating the contribution of storms as well as annual precipitation to groundwater recharge and its circulation, in the semi‐arid region of Bagepalli, Kolar district, Karnataka. Environmental isotopes ²H, ¹⁸O and ³H were used to study the effect of storms on the hydrological system, and an isotope balance was used to compute the contribution of a storm component to the groundwater. Some of the groundwater samples collected during the post‐storm periods were highly depleted in stable isotope content with higher deuterium excess relative to groundwater from the pre‐storm periods. Significant variation in deuterium excess in groundwater from the same area, collected in two different periods, indicates the different origin of air masses. The estimated recharge component of a storm event of 600 mm to the groundwater was found to be in the range of 117–165 mm. There was no significant variation in environmental tritium content of post‐storm and pre‐storm groundwater, indicating the fast circulation of groundwater in the system. After completion of the environmental isotope work, an injected radiotracer ³H technique was applied to estimate the direct recharge of total precipitation to the groundwater. The estimated recharge to the groundwater is 33 mm of the 550 mm annual precipitation during 1992. Copyright © 2003 John Wiley & Sons, Ltd.     

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.