A discontinuous climatic record from 187 to 74 ka from a speleothem of the Clamouse Cave (south of France)

This study presents a continental paleoclimatic record in the south of France, based on δ¹⁸O, δ¹³C and the ²³⁴U/²³⁸U activity ratio, dated by the ²³⁰Th/²³⁴U disequilibrium method with thermal ionization mass spectrometry. A stalagmite (Cla4) from the Clamouse Cave offers a discontinuous stable isotopic record between 189 ka and 74 ka which covers marine isotope stages (MIS) 7, 6.4, 5.5, 5.3 and 5.1. The growth phases of the Cla4 stalagmite correspond to high sea level stages, except during MIS 6.4 (169-162 ka). All the growth phases of Cla4 correspond to humid periods, corresponding to the sapropel events observed in the eastern Mediterranean basin. Thus, the influence of a strong hydrological activity in the eastern Mediterranean basin during these periods prevailed as far west as the south of France. Because the karstic system studied strongly buffers the isotopic composition of water, isotopic variations of the calcite deposited in the cave represent mainly global and large-scale environmental variations when isotopic equilibrium conditions prevailed for calcite crystallization. Sub-stage 5.3, the end of 5.5 and MIS 7 were colder by about 4-6°C (calculated temperature) compared to present-day temperature while the growth phases of sub-stages 5.1 and the beginning of 5.5 reflect environmental conditions close to present ones. The δ¹⁸O and δ¹³C values of cave deposits of the sub-stage 6.4 are: (1) strongly marked by kinetic fractionation processes such as evaporation due to moisture deficit within the cave atmosphere during the first step of this growth phase and (2) related to higher humidity due to a second period of enhanced rainfall during the second step of growth. This study shows that even if calcite has not been deposited at isotopic equilibrium, its isotopic composition can give insights into the environmental conditions at the time of deposition.     

Sub-Milankovitch climatic cycles in Holocene stalagmites from Sauerland, Germany

Calcitic stalagmites from caves in the Sauerland, Germany, prove the existence of sub-Milankovitch cycles in precipitation during the last 6000 yr. The δ¹⁸O record dated with Th/U is interpreted as an indicator of paleohumidity. Spectral analysis of δ¹⁸O from 6000 a BP up to the recent top of a stalagmite from the Atta cave yields statistically significant peaks at 1450, 117, 64 and 57 a. Additionally we find a good correlation of the stalagmite’s δ¹⁸O and Δ¹⁴C from European tree rings. The 1450 a cycle in the stalagmite probably is analogous to the pervasive millennial scale climate cycle described by Bond et al. [Science 278 (1997) 1257-1266; 294 (2001) 2130-2136] derived from the amount of ice rafted debris in deep sediments from the North Atlantic. Our results suggest that the centennial to millennial shifts observed in the North Atlantic are accompanied by synchronous shifts of the climate in Northern and Central Europe, which most probably can be attributed to solar irradiation variations.     

Two modes of climatic control in the Holocene stalagmite record from the Japan Sea side of the Japanese islands

The Holocene stalagmite FG01 collected at the Fukugaguchi Cave in Itoigawa, central Japan provides a unique high‐resolution record of the East Asian winter monsoon. Because of the climate conditions on the Japan Sea side of the Japanese islands, the volume of precipitation during the winter is strongly reflected in the stalagmite δ¹⁸O signal. Examination of the carbon isotopes and the Mg/Ca ratio of FG01 provided additional information on the Holocene climate in Itoigawa, which is characterized by two different modes separated at 6.4 ka. Dripwater composition and the correlation between the δ¹³C and Mg/Ca data of FG01 indicate the importance of prior calcite precipitation (PCP), a process that selectively eliminated ¹²C and calcium ions from infiltrating water from CO₂ degassing and calcite precipitation. In an earlier period (10.0–6.4 ka), an increase in soil pCO₂ associated with warming and wetting climate trends was a critical factor that enhanced PCP, and resulted in an increasing trend in the Mg/Ca and δ¹³C data and a negative correlation between the δ¹³C and δ¹⁸O profiles. A distinct peak in the δ¹³C age profile at 6.8 ka could be a response to an increase of approximately 10% in C4 plants in the recharge area. At 6.4 ka, the climate mode changed to another, and correlation between δ¹⁸O and δ¹³C became positive. In addition, a millennial‐scale variation in δ¹⁸O and pulsed changes in δ¹³C and Mg/Ca became distinct. Assuming that δ¹⁸O and PCP were controlled by moisture in the later period, the volume of precipitation was high during 6.0–5.2, 4.4–4.0, and 3.0–2.0 ka. In contrast, the driest interval in Itoigawa was during 0.2–0.4 ka, and broadly corresponds to the Little Ice Age.     

A possible Younger Dryas-type event during Asian monsoonal Termination 3

1 Introduction The Younger Dryas (YD) cold spell is one of the most prominent abrupt climate change events in the past and a key feature of the last glacial termination. A great agreement has been attained in terms of the tim- ing and geographic extent of…     

An isotopic calibration study of precipitation,cave dripwater,and climate in west‐central Florida

A calibration study of oxygen and hydrogen isotopic composition from precipitation and cave dripwater was conducted in west‐central Florida at Legend Cave during 2007–2008. This study was performed to better understand how modern precipitation patterns can be discerned through examination of cave dripwater and speleothem calcite for paleoclimate reconstruction. The ‘amount effect’ was shown to be a dominant control on the oxygen isotopic composition of precipitation for the study area. A meteoric water line with a slope of 6·7 suggests evaporative effects occur either during precipitation or subsequent hydrological processes. However, δ¹⁸O values of cave dripwater averaged near the mean annual amount‐weighted average of precipitation, suggesting that the isotopic composition of dripwater tracks the long‐term average of rainfall. An observed weak seasonal influence occurred in the d‐excess values, with summer precipitation being more enriched due to increased evaporative effects. Comparison of precipitation δ¹⁸O values to synoptic weather data shows the dominant amount effect influence occurs due to strong convective storms producing highly ¹⁸O‐depleted rainfall at greater amounts during the year. Constant δ¹⁸O values of the dripwater indicate that paleoclimate reconstructions using speleothems from this area would record changes in annual to interannual shifts in precipitation amount above the cave. Copyright © 2011 John Wiley & Sons, Ltd.     

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.     

Stalagmite from the Austrian Alps reveals Dansgaard-Oeschger events during isotope stage 3:: Implications for the absolute chronology of Greenland ice cores

A mass-spectrometric uranium-series dated stalagmite from the Central Alps of Austria provides unprecedented new insights into high-altitude climate change during the peak of isotope stage 3. The stalagmite formed continuously between 57 and 46 kyr before present. A series of ‘Hendy tests’ demonstrates that the outer parts of the sample show a progressive increase of both stable C and O isotope values. No such covariant increase was detected within the axial zone. This in conjunction with other observations suggests that the continuous stable oxygen isotope profile obtained from the axial zone of the stalagmite largely reflects the unaltered isotopic composition of the cave drip water. The δ¹⁸O record shows events of high δ¹⁸O values that correlate remarkably with Interstadials 15 (a and b), 14 and 12 identified in the Greenland ice cores. Interstadial 15b started rapidly at 55.6 kyr and lasted ∼300 yr only, Interstadial 15a peaked 54.9 kyr ago and was even of shorter duration (∼100 yr), and Interstadial 14 commenced 54.2 kyr ago and lasted ∼3000 yr. This stalagmite thus represents one of the first terrestrial archives outside the high latitudes which record precisely dated Dansgaard-Oeschger (D/O) events during isotope stage 3. Provided that rapid D/O warmings occurred synchronously in Greenland and the European Alps, the new data provide an independent tool to improve the GRIP and GISP2 chronologies.     

Factors controlling spatial and seasonal distributions of precipitation δ18O in China

Utilising datasets from the Global Network of Isotopes in Precipitation of the International Atomic Energy Agency, and previous isotopic studies, we investigated δ¹⁸O spatial and temporal patterns in Chinese precipitation. Significantly positive relationships existed between precipitation δ¹⁸O and air temperature above the north of 35°N and in high altitude regions above 32°N. Significantly negative relationships between precipitation δ¹⁸O and the precipitation amount existed below south of 35°N. These temperature and precipitation effects became stronger with increasing altitude except in high altitude regions between 32°N and 35°N. The NCEP/NCAR reanalysis data from 1980 to 2004 showed that variations in spatial and seasonal wind fields at 700 hpa and total precipitable water from the ground to the top of the atmosphere were correlated with the monthly spatial distribution of precipitation δ¹⁸O. Basing on this relationship, we established quantitative correlations between the mean monthly precipitation δ¹⁸O and both latitude and temperature in different seasons. We found that spatial variations in precipitation δ¹⁸O could be described well using the Bowen–Wilkinson model and second‐order equations developed during the present study only in winter (from December to February). During the rest of the year, patterns were too complex to predict using simple models. The results suggest that it is difficult to demonstrate variations of precipitation δ¹⁸O throughout the year and for all regions of China using a single model. Moreover, the new models for the relationships among precipitation, latitude, and temperature were better able to depict the variations in precipitation δ¹⁸O than the Bowen–Wilkinson model. Copyright © 2011 John Wiley & Sons, Ltd.     

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.     

Kinetic processes and stable isotopes in cave dripwaters as indicators of winter severity

We examine how the stable isotope composition of meteoric water is transmitted through soil and epikarst to dripwaters in a cave in western Romania. δ²H and δ¹⁸O in precipitation at this site are influenced by temperature and moisture sources (Atlantic and Mediterranean), with lower δ¹⁸O in winter and higher in summer. The stable isotope composition of cave dripwaters mimics this seasonal pattern of low and high δ¹⁸O, but the onset and end of freezing conditions in the winter season are marked by sharp transitions in the isotopic signature of cave dripwaters of approximately 1 ‰. We interpret these shifts as the result of kinetic isotopic fractionation during the transition phase from water to ice at the onset of freezing conditions and the input of meltwater to the cave at the beginning of the spring season. This process is captured in dripwaters and therefore speleothems from Ur?ilor Cave, which grew under such dripping points, may have the potential to record past changes in the severity of winters. Similar isotopic changes in dripwaters driven by freeze–thaw processes can affect other caves in areas with winter snow cover, and cave monitoring during such changes is essential in linking the isotopic variability in dripwaters and speleothems to surface climate.     

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.     

Vapour source and spatiotemporal variation of precipitation isotopes in Southwest Spain

The δ²H and δ¹⁸O composition of 77 precipitation samples collected between January 2014 and April 2019 from two sites across the Guadalquivir Basin, SW Spain, were analysed. The first site is located in an urban area of Seville at 100 km distance to the Atlantic coast and the second site is located in a dune area of the Doñana National Park a few kilometres from the coast. Sampling was performed within intervals of at least 14 days if rain occurred but frequently intervals were longer according to the rainfall incidence. Samples from both sites are available for the period February 2016 to June 2018 with six samples containing identical rain events at both locations. Precipitation weighted averages and local meteoric water lines produced by weighting and non-weighting regression methods are presented for its use in hydrological applications. Results show a remarkably high variability in δ²H and δ¹⁸O values and precipitation weighted average d-excess values of 11.8‰ and 13‰ at the sites Plaza de España and Doñana, respectively. Temperature and amount effects were found to be weak. A significant influence of secondary evaporation for single rainfall events during summer was identified by enriched isotopic signatures with reduced d-excess values plotting close or below the global meteoric water line. Backward trajectory analysis of 115 days with daily rainfall above 3 mm yield a predominant Atlantic Ocean vapour source with negligible Mediterranean influence and therefore, d-excess variability is attributed to the different ocean surface conditions of relative humidity and sea surface temperature. Parallel sampling indicate very similar isotopic signatures at both sites and point to the existence of thermal effects of the Plaza de España site in Seville city during the summer season.     

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.     

Applicability of isotopic hydrograph separation in a suburban basin during snowmelt

C. H. TAYLOR Methodological issues associated with isotopic hydrograph separations (IHSs) in built-up environments are explored using results from the 1990 spring melt in a suburban basin in Peterborough, Ontario, Canada. The hetrogeneous nature of suburban environments complicates the selection of appropriate isotopic signatures for event and pre-event waters. Near-stream groundwater δ¹⁸O sampled from wells was poorly mixed, such that the pre-event water signature was best characterized by δ¹⁸O in pre-melt baseflow or discharge from a headwater spring. The event water signature during snowmelt can be characterized using δ¹⁸O in the pre-melt snowpack, surface runoff samples or meltwater from lysimeters. However, the use of snowpack δ¹⁸O may be inappropriate in suburban basins where meltwater from thin snowcover may exhibit pronounced responses to δ¹⁸O in rainfall contributions. Intensive sampling of the spatial variability of runoff or meltwater δ¹⁸O may be required to characterize the average event water signature adequately. Rainfall δ¹⁸O provided an appropriate event water signal during a large rain on snow event, and differences between this IHS and one generated using an event water signature that included meltwater contributions from snow-covered surfaces were within the uncertainty attributable to the analytical error in δ¹⁸O values. Event water supplied 55-63% of the peak discharge and 48-58% of total runoff from the basin during the melt, which is consistent with the fraction of the basin that has been developed. These results contrast with IHSs conducted in forested basins that suggest that stormflow is dominated by pre-event water contributions.     

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.     

Relation between stable isotope in monsoon precipitation in southern Tibetan Plateau and moisture transport history

The moisture transport history to the south of the Tibetan Plateau was modeled using the meteorological data provided by NCEP in this paper, and the modeled results were compared with the measured δ¹⁸O in the south of the Tibetan Plateau. The relation between δ¹⁸O in precipitation in the south of the Tibetan Plateau and moisture trajectories was discussed. The results show that the extremely low δ¹⁸O in precipitation in the south of the Tibetan Plateau is always related to the moisture from the low-level sea surface evaporation. The long-distance transport of moisture also contributes to low δ¹⁸O in precipitation probably due to the rainout process during moisture transport. It is also found that low δ¹⁸O in precipitation is also related with deep layer transport of moisture, and with intensive condensation in the upper layers of the atmosphere, resulting in low δ¹⁸O because of depletion of heavy isotopes in deep condensation. However, high δ¹⁸O in precipitation whether in monsoon period or not is always companied with moisture coming from the upper layers, and the moisture is from northern or western sides of the plateau. The interpretation of the modeled results is in agreement with the isotope fractionation processes.

     

Using stable isotopes of surface water and groundwater to quantify moisture sources across the Yellow River source region

Characterization of stable isotope compositions (δ²H and δ¹⁸O) of surface water and groundwater in a catchment is critical for refining moisture sources and establishing modern isotope–elevation relationships for paleoelevation reconstructions. There is no consensus on the moisture sources of precipitation in the Yellow River source region during summer season. This study presents δ²H and δ¹⁸O data from 111 water samples collected from tributaries, mainstream, lakes, and groundwater across the Yellow River source region during summertime. Measured δ¹⁸O values of the tributaries range from ?13.5‰ to ?5.8‰ with an average of ?11.0‰. Measured δ¹⁸O values of the groundwater samples range from ?12.7‰ to ?10.5‰ with an average of ?11.9‰. The δ¹⁸O data of tributary waters display a northward increase of 1.66‰ per degree latitude. The δ¹⁸O data and d‐excess values imply that moisture sources of the Yellow River source region during summertime are mainly from the mixing of the Indian Summer Monsoon and the Westerlies, local water recycling, and subcloud evaporation. Analysis of tributary δ¹⁸O data from the Yellow River source region and streamwater and precipitation δ¹⁸O data from its surrounding areas leads to a best‐fit second‐order polynomial relationship between δ¹⁸O and elevation over a 4,600 m elevation range. A δ¹⁸O elevation gradient of ?1.6‰/km is also established using these data, and the gradient is in consistence with the δ¹⁸O elevation gradient of north and eastern plateau. Such relationships can be used for paleoelevation reconstructions in the Yellow River source region.     

Continuous monitoring of stream δ18O and δ2H and stormflow hydrograph separation using laser spectrometry in an agricultural catchment

A portable Wavelength Scanned‐Cavity Ring‐Down Spectrometer (Picarro L2120) fitted with a diffusion sampler (DS‐CRDS) was used for the first time to continuously measure δ¹⁸O and δ²H of stream water. The experiment took place during a storm event in a wet tropical agricultural catchment in north‐eastern Australia. At a temporal resolution of one minute, the DS‐CRDS measured 2160 δ¹⁸O and δ²H values continuously over a period of 36 h with a precision of ±0.08 and 0.5‰ for δ¹⁸O and δ²H, respectively. Four main advantages in using high temporal resolution stream δ¹⁸O and δ²H data during a storm event are highlighted from this study. First, they enabled us to separate components of the hydrograph, which was not possible using high temporal resolution electrical conductivity data that represented changes in solute transfers during the storm event rather than physical hydrological processes. The results from the hydrograph separation confirm fast groundwater contribution to the stream, with the first 5 h of increases in stream discharge comprising over 70% pre‐event water. Second, the high temporal resolution stream δ¹⁸O and δ²H data allowed us to detect a short‐lived reversal in stream isotopic values (δ¹⁸O increase by 0.4‰ over 9 min), which was observed immediately after the heavy rainfall period. Third, δ¹⁸O values were used to calculate a time lag of 20 min between the physical and chemical stream responses during the storm event. Finally, the hydrograph separation highlights the role of event waters in the runoff transfers of herbicides and nutrients from this heavily cultivated catchment to the Great Barrier Reef. Copyright © 2015 John Wiley & Sons, Ltd.     

Isotopic temporal and spatial variations of tropical rivers in Thailand reflect monsoon precipitation signals

Stable isotopic compositions (δ¹⁸O and d-excess) from 25 rivers in Thailand were analysed monthly during 2013–2015. Results indicated that monsoon precipitation fundamentally influences the river isotopes. The overland flow supplied from monsoon precipitation and human-altered flow regimes produces considerable isotopic variability. Spatial and temporal variations were observed among four principal geographical regions. The seasonality of monsoon precipitation in mountainous Thailand produced large variations in isotopic compositions because most rainfall occurred during the southwest monsoon, and dry conditions prevailed during the northeast monsoon. The northern and northeastern regions are mountainous, highland areas. Low δ¹⁸O values were found in these regions, likely because of altitude effects on precipitation. Conversely, monsoonal precipitation continually supplies rivers in southern Thailand all year round, producing higher and more consistent δ¹⁸O values than in the other regions. The Chao Phraya plain in the central region experienced enrichment of δ¹⁸O river runoff related to evaporation in irrigation systems. Larger catchment areas and longer residence times resulted in more pronounced evaporation effects, producing lower values of d-excess and local river water line slopes compared with precipitation. The isotopic differences between river waters and precipitation were utilized to determine river recharge elevations and water transit time. The methods presented here can be used to explore hydrological interactions in other tropical river basins.     

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.