Water Isotope Ratios Research Articles

The relationship of δD and δ18O in soil water and its implications for soil evaporation across distinct rainfall years in winter wheat field in the North China Plain

Soil evaporation plays a key role in regulating local climate and water loss. Stable isotope ratios of water (²H/¹H and ¹⁸O/¹⁶O) are effective tracers for studying water flux. This study examines three isotope-based indicators deuterium excess (d-excess), the slope of the soil water evaporation line (SEL), and line-conditioned excess (lc-excess) across three wheat growing seasons: wet, ordinary, and dry years. The influencing factors of d-excess, SEL, and lc-excess, respectively, soil, vegetation, and meteorology, were analyzed using various methods. Wheat yields varied significantly, reaching 6.69 t ha⁻¹ in wet years, 8.66 t ha⁻¹ in dry years, and 9.28 t ha⁻¹ in ordinary years. The lc-excess was highest in ordinary years, and d-excess peaked during dry years. A negative correlation between d-excess and SEL slope, and between lc-excess and SEL slope, was observed in dry and ordinary years (P<0.05), but not in wet years (P>0.05). Multivariate regression showed that net radiation (Rn) was the primary factor influencing SEL, contributing 54.19 %, 11.58 %, and 29.27 % in wet, dry, and ordinary years, respectively. Leaf area index (LAI) was the most significant factor affecting lc-excess (37.91 % in wet years, 32.22 % in dry, and 30.92 % in ordinary years). Vapor pressure deficit (VPD) affected d-excess in wet and ordinary years, while air (Ta) and soil temperature (Ts) were key in dry years. Variation partitioning revealed meteorological factors primarily influenced SEL, lc-excess, and d-excess in wet years, while soil, vegetation, and climate interactions had greater effects in dry and ordinary years. The lc-excess, integrating multiple factors, is a better indicator of soil evaporation than SEL.

An urbanized phantom tributary subsidizes river–riparian communities of a mainstem gravel‐bed river

Abstract Urbanization transforms natural river channels, and surface water of some rivers disappeared over time. How and whether the subsurface domains of the original waterways and aquifers connecting them (a phantom of historical landscape) are functional is not known. This study examined the effects of tributary groundwater inflow on the response of river–riparian organisms in an alluvial mainstem river in northern Japan, where the tributary disappeared over the course of urban landscape transformation. A 2.8‐km lowland segment of the mainstem gravel‐bed river was examined for water properties and the river–riparian food web. In addition, watershed‐wide water sampling was conducted to isotopically distinguish several types of groundwater that contributed to the hyporheic water in the study segment. Altitude had a clear effect on the hydrogen/oxygen stable isotope ratios in the river water collected across the watershed. Groundwater unique both in chemical and isotopic signatures occurred in several spots within the study segment, and its properties resembled and its upwelling locations matched groundwater from a tributary river whose surface channel disappeared 60 years ago. Positive numerical increases in abundance and/or a sign of nitrogen transfer in river–riparian communities (algae, invertebrates and riparian trees) originating from groundwater high in nitrate with elevated nitrogen stable isotope ratios were found. We demonstrated that tributary groundwater with unique chemical properties manifested by an urban watershed river network continued to have trophic effects on biota across the river–riparian boundary in the mainstem river, even after urbanization transformed the tributary into a phantom river. We highlighted the legacy effects of landscape transformation in the subsurface domain and the significance of scrutinizing the past landscape and hydrological connectivity at the watershed scale in urban environments.

An East Antarctic, sub-annual resolution water isotope record from the Mount Brown South Ice core

We report high resolution measurements of the stable water isotope ratios (δ18O, δD) from the Mount Brown South ice core (MBS, 69.11° S 86.31° E). The record covers the period 873 - 2009 CE with sub-annual temporal resolution. Preliminary analyses of surface cores have shown the Mount Brown South site has relatively high annual snowfall accumulation (0.3 metres ice equivalent) with a seasonal bias toward lower snowfall during austral summer. Precipitation at the site is frequently related to intense, short term synoptic scale events from the mid-latitudes of the southern Indian Ocean. Higher snowfall regimes are associated with easterly winds, while lower snowfall regimes are associated with south-easterly winds. Isotope ratios are measured with Infra-Red Cavity Ring Down Spectroscopy, calibrated on the VSMOW/SLAP scale and reported on the MBS2023 time scale interpolated accordingly. We provide estimates for measurement precision and internal accuracy for δ18O and δD.

Water isotope ratios reflect convection intensity rather than rain type proportions in the pantropics.

Against the traditional view, a recently published theory argued that isotope ratios are higher in convective precipitation but lower in stratiform precipitation and proposed that isotope ratios reflect rain type proportions. This theory has been widely cited despite some early reservations. Whether the theory represents a faithful reflection of signals of water isotope ratios remains unclear. Here, we reassess its validity from different timescales and broader observations from the pantropics. Unexpectedly, our findings contradict the theory on daily, monthly, and even annual timescales. Pantropical precipitation isotope ratios remain strongly correlated to convection intensity but are independent of rain type proportions because stratiform precipitation isotope ratios cover a large range of values. We find that the theory has many serious weaknesses related to preferential data selection and suggest that new theories need to be validated at more locations on different timescales before gaining widespread acceptance.

Hydrologic source identification using stable isotope ratios of bottled drinking water in Egypt

A convenient way to understand hydrologic source identification is to make use of a suitable tracer. Isotopes of oxygen and hydrogen provide that opportunity since the isotope ratios of the primary source, precipitation, can be modified by post precipitation processes. This approach has been tested by carrying out a comprehensive isotope ratios investigation of domestic and imported bottled water sourced and distributed across Egypt. Our collection of bottled water includes 33 samples distributed under 27 distinct brands. We compare the isotope ratios of the bottled water with the isotope ratios of the reported natural water source of this water. The bottled water isotope ratios preserve information about the water sources from which they were derived. The measured oxygen and hydrogen ratios of the studied bottled water samples range from −11.51‰ to 2.94‰, with an average value of −1.89‰ for δ18O and from −81.69‰ to 23.94‰, with an average value of −9.54‰ for δ2H. The observed variability of isotope ratios in the bottled water falls within the span of the natural groundwater resources in Egypt, such as shallow and deep groundwater aquifers as well as claimed non-Egyptian sources. In general, the bottled water samples in the data set can be divided into four distinct groups based on their isotope ratios. One group represents imported bottled water brands, and three groups include domestic brands. The first group represents the imported bottled water brands. Their measured isotopic compositions are similar to those of their claimed sources. The second group has the lowest δ18O and δ2H values and likely originated from the Nubian aquifer. The third and fourth groups appear to have been sourced from the Nile Valley and Delta aquifer. The third group isotopic content and d-excess values indicate a higher degree of mixing with evaporated return flow water. The results provided in this study indicate the diverse hydrogeology of the local bottled water brands. This promises extending the approach to several sites globally.

Isotopic evaluation of the National Water Model reveals missing agricultural irrigation contributions to streamflow across the western United States.

The National Water Model (NWM) provides critical analyses and projections of streamflow that support water management decisions. However, the NWM performs poorly in lower-elevation rivers of the western United States (US). The accuracy of the NWM depends on the fidelity of the model inputs and the representation and calibration of model processes and water sources. To evaluate the NWM performance in the western US, we compared observations of river water isotope ratios ( and expressed in notation) to NWM-flux-estimated (model) river reach isotope ratios. The modeled estimates were calculated from long-term (2000-2019) mean summer (June, July, and August) NWM hydrologic fluxes and gridded isotope ratios using a mass balance approach. The observational dataset comprised 4503 in-stream water isotope observations in 877 reaches across 5 basins. A simple regression between observed and modeled isotope ratios explained 57.9 % ( ) and 67.1 % ( ) of variance, although observations were 0.5 ‰ ( ) and 4.8 ‰ ( ) higher, on average, than mass balance estimates. The unexplained variance suggest that the NWM does not include all relevant water fluxes to rivers. To infer possible missing water fluxes, we evaluated patterns in observation-model differences using ( ) and ( ). We detected evidence of evaporation in observations but not model estimates (negative and positive ) at lower-elevation, higher-stream-order, arid sites. The catchment actual-evaporation-to-precipitation ratio, the fraction of streamflow estimated to be derived from agricultural irrigation, and whether a site was reservoir-affected were all significant predictors of in a linear mixed-effects model, with up to 15.2 % of variance explained by fixed effects. This finding is supported by seasonal patterns, groundwater levels, and isotope ratios, and it suggests the importance of including irrigation return flows to rivers, especially in lower-elevation, higher-stream-order, arid rivers of the western US.

High-Precision and Real-Time Measurement of Water Isotope Ratios Based on a Mid-Infrared Optical Sensor.

A compact spectrometer based on a mid-infrared optical sensor has been developed for high-precision and real-time measurement of water isotope ratios. The instrument uses laser absorption spectroscopy and applies the weighted Kalman filtering method to determine water isotope ratios with high precision and fast time response. The precision of the measurements is 0.41‰ for δ18O and 0.29‰ for δ17O with a 1 s time. This is much faster than the standard running average technique, which takes over 90 s to achieve the same level of precision. The successful development of this compact mid-infrared optical sensor opens up new possibilities for its future applications in atmospheric and breath gas research.

Uranium-series and strontium isotope systematics in soil carbonates from dryland Critical Zones: Implications for soil inorganic carbon storage and transformation

Soil carbonates are dominantly present in dryland Critical Zone (CZ) and their formation could lead to important long-term carbon sequestration in arid to semiarid soils if the Ca ions were derived from silicate weathering or other non-carbonate sources. In managed CZ systems such as agricultural areas converted from natural drylands, irrigation has profound effects on the dryland CZ inorganic carbon storage, especially by modifying dissolution and precipitation dynamics of soil carbonates via controls of irrigation intensity and water chemistry, soil properties, and hydrological flow paths. These processes could lead to transformation of inorganic carbon in soils and groundwater aquifers underneath drylands. One key knowledge gap in studying soil carbonates from managed dryland CZ systems is to detect the formation of soil carbonates under irrigated conditions and distinguish them effectively from soil carbonates formed under natural conditions.Here, we explore the potential of using U-series and strontium isotopes to investigate the formation timescales and conditions of soil carbonates in both natural and managed dryland CZ in Chihuahua Desert of American Southwest. We obtained new U-series and Sr isotope ratios from mature stage V natural soil carbonates in the Jornada Basin of southern New Mexico and compared to previously published U-series and Sr isotope results for younger Jornada soil carbonates as well as irrigation impacted soil carbonates from the Rio Grande floodplains in west Texas. Specifically, we applied the U-series dating method (238U-234U-230Th) to estimate the timescales of soil carbonate formation under both natural climatic conditions and impacts of modern agriculture irrigation. In addition, we showed that the initial (234U/238U) activity ratios recorded in these soil carbonates reflect the systematic changes of soil infiltration rates in both natural and managed dryland CZ. We also utilized Sr isotope ratios (87Sr/86Sr) in soil carbonates, dust, and irrigation water to trace the Ca sources in soil carbonates from natural and managed dryland CZ. Soil carbonates from both settings were characterized by slightly radiogenic 87Sr/86Sr ratios, consistent with their potential of long-term carbon storage in drylands.U-series and Sr isotope systematics characterize important differences in soil carbonates from natural and managed dryland CZ with respect to their Ca sources, timescales of carbonate formation and transformation, and availability of soil moisture. Soil carbonates formed, accumulated, and transformed in natural drylands with long time scales but under irrigated arid agricultural areas its formation is significantly modified by irrigation and other agriculture practices, with implications for long- and short-term inorganic carbon sequestration in both systems of drylands.

An annually resolved chronology for the Mount Brown South ice cores, East Antarctica

Abstract. Climate reconstructions of the last millennium rely on networks of high-resolution and well-dated proxy records. This study presents age-at-depth data and preliminary results from the new Mount Brown South (MBS) ice cores, collected at an elevation of 2084 m on the boundary of Princess Elizabeth Land and Kaiser Wilhelm II Land in East Antarctica. We show an initial analysis of the site meteorology, mean annual chemical species concentrations and seasonal cycles, including the identification of a seasonal cycle in fluoride concentrations. The annually resolved chronologies were developed from the chemistry data using a site-specific layer-counting methodology that employed seasonally varying trace chemical species and stable water isotopic ratios, combined with alignment to known volcanic horizons. The uncertainty in the determination of annual horizons via layer counting was also quantified. The chronologies developed include the “Main” 295 m record spanning 1137 years (873–2009 CE) and three surface cores spanning the most recent 39–52 years up to the surface age at the time of drilling (austral summer 2017/2018). Mean annual trace chemical concentrations are compared to the Law Dome ice core (located 1130 km east of the Mount Brown South site) and discussed in terms of atmospheric transport. The MBS chronologies presented here – named MBS2023 – will underpin the development of new palaeoclimate records spanning the past millennium from this under-represented region of East Antarctica.

Abrupt Geographic Shift in Hydrogen Isotope Ratios of Meteoric Water Across the Western Andes, Peru

AbstractQuantitative isotopic paleoaltimetry has been applied in regions where Rayleigh distillation controls isotopic lapse rates. Air mass mixing and moisture recycling are viewed as complicating factors. We show here that, because of such effects, a cross‐Andean transect of meteoric water δD values precisely marks the geographic position of the Western Cordillera crest. This modern water signal is also recorded in Pliocene‐Pleistocene hydrated volcanic glass δD values. δD values between the Pacific coast and Western Cordillera exhibit no trend up to 2.5 km elevation and 100 km inboard, consistent with an arid climate in which Amazonian moisture is topographically blocked and Pacific moisture is efficiently recycled. The result is a large δD lapse rate (−98‰/km) and an abrupt horizontal δD shift (2‰/km) at the Western Cordillera crest. Therefore, we conclude that cross‐orogen δD transects could locate the ancient Western Cordillera crest.

Bidirectional energy subsidies for fish in river mouths of a large lake as revealed by stable isotopes and fatty acids

AbstractFreshwater river mouths may facilitate cross‐habitat resource use and bidirectional subsidization through (a) active cross‐habitat movement by consumers like fish and (b) water and material movement both downstream, from tributary to nearshore lake, and in the opposite direction due to backflow processes. Despite potential importance of freshwater river mouths, relative contributions of lentic and tributary energy sources to fishes along these ecotones remain understudied, in part because measuring cross‐habitat subsidization is not straightforward. We assessed cross‐habitat subsidization of three fish consumers round goby (Neogobius malanostomus), yellow perch (Perca flavescens), and alewife (Alosa psuedoharengus) in three river mouths of Lake Michigan, USA. Specifically, we (a) measured stable isotope ratios (δ13C, δ15N, δ2H, δ18O) in ambient water, bivalve shells, potential invertebrate prey, and fish soft tissue, and we assessed fish nutritional status based on essential fatty acid composition, and (b) estimated Bayesian ellipses and mixing models including either two (δ13C‐δ15N) or three (δ13C‐δ15N‐δ2H) isotope ratios. Results revealed evidence of bidirectional habitat subsidies for all fishes, but energy subsidies varied by species and across river mouths; likely related to differences in species‐specific behavior and hydrologic differences among river mouths. Relative to nearshore oligotrophic Lake Michigan, fish in productive tributary environments contained relatively low essential fatty acid content, suggesting a possible trade‐off between prey quantity and quality across habitats. This study advances our understanding of resource connectivity in lake ecosystems and the combined use of multiple stable isotopes (including mixing models) and fatty acids to document cross‐habitat subsidies along freshwater ecotones.

Investigating strontium isotope linkage between biominerals (uroliths), drinking water and environmental matrices

This study presents the mineralogy and strontium isotope ratio (87Sr/86Sr) of 21 pathological biominerals (bladder and kidney stones) collected from patients admitted between 2018 and 2020 at the Department of Urology of the San Pio Hospital (Benevento, southern Italy). Urinary stones belong to the calcium oxalate, purine or calcium phosphate mineralogy types. Their corresponding 87Sr/86Sr range from 0.707607 for an uricite sample to 0.709970 for a weddellite one, and seem to be partly discriminated based on the mineralogy. The comparison with the isotope characteristics of 38 representative Italian bottled and tap drinking waters show a general overlap in 87Sr/86Sr with the biominerals. However, on a smaller geographic area (Campania Region), we observe small 87Sr/86Sr differences between the biominerals and local waters. This may be explained by external Sr inputs for example from agriculture practices, inhaled aerosols (i.e., particulate matter), animal manure and sewage, non-regional foods. Nevertheless, biominerals of patients that stated to drink and eat local water/wines and foods every day exhibited a narrower 87Sr/86Sr range roughly matching the typical isotope ratios of local geological materials and waters, as well as those of archaeological biominerals from the same area.Finally, we conclude that the strontium isotope signature of urinary stones may reflect that of the environmental matrices surrounding patients, but future investigations are recommended to ultimately establish the potential for pathological biominerals as reliable biomonitoring proxies, taking into the account the contribution of the external sources of Sr.

Application of gas chromatography-stable isotope mass spectrometry to determine the oxygen isotope ratio of water in concentrated fruit juice

In this study, we developed a method to determine the authenticity of concentrated fruit juice using the δ18O ratio of water. We utilized the gas chromatography-isotope ratio mass spectrometry (GC-IRMS) technique along with the offline isotope exchange equilibrium method to pretreat and measure the oxygen isotopes in water in concentrated apple juice. This innovative approach uses anhydrous ethanol as a solvent to dissolve concentrated juices, thereby facilitating a more comprehensive reaction between the water in the sample and the CO2 standard gas. Additionally, the reaction vessel exhibits excellent air tightness, ensuring rapid equilibrium time and enabling accurate determination of δ18O in the water content of concentrated juice. The reaction vessel had excellent air tightness and rapid equilibration time, enabling accurate measurement of δ18O of water in concentrated fruit juice. The reaction vessel used had excellent air tightness and rapid equilibration time, ensuring accurate measurement of the δ18O of water in concentrated fruit juice. We analyzed 40 samples of concentrated apple juice and found that the range of δ18O values in the water of concentrated apple juice was between 1.29 ‰ and 7.59 ‰. Additionally, we used prepared sucrose syrup as a simulated sample and found that the δ18O distribution range was between −10.43 ‰ and −10.53 ‰. Furthermore, we conducted adulteration simulation experiments on randomly selected real samples and discovered a linear negative correlation between the adulteration ratio and the δ18O value of water in the samples.

Microbial methane formation in deep aquifers associated with the sediment burial history at a coastal site

Abstract. Elucidating the mechanisms underlying microbial methane formation in subsurface environments is essential to understanding the global carbon cycle. This study examined how microbial methane formation (i.e., methanogenesis) occurs in natural-gas-bearing sedimentary aquifers throughout the sediment burial history. Water samples collected from six aquifers of different depths exhibited ascending vertical gradients in salinity from brine to fresh water and in temperature from mesophilic to psychrophilic conditions. Analyses of gas and water isotopic ratios and microbial communities indicated the predominance of methanogenesis via CO2 reduction. However, the hydrogen isotopic ratio of water changed along the depth and salinity gradient, whereas the ratio of methane changed little, suggesting that in situ methanogenesis in shallow sediments does not significantly contribute to methane in the aquifers. The population of methane-producing microorganisms (methanogens) was highest in the deepest saline aquifers, where the water temperature, salinity, and total organic carbon content of the adjacent mud sediments were the highest. Cultivation of the dominant hydrogenotrophic methanogens in the aquifers showed that the methanogenesis rate was maximized at the temperature corresponding to that of the deepest aquifer. These results suggest that high-temperature conditions in deeply buried sediments are associated with enhanced in situ methanogenesis and that methane that forms in the deepest aquifer migrates upward into the shallower aquifers by diffusion.

Detection of dilution due to turbulent mixing vs. precipitation scavenging effects on biomass burning aerosol concentrations using stable water isotope ratios during ORACLES

Abstract. The interaction between biomass burning aerosols and clouds remains challenging to accurately determine, in part because of difficulties using direct observations to account for influences on aerosol concentrations from precipitation scavenging and dilution due to air mass mixing and separating those signals from source contributions. The prevalence of mixing versus precipitation processes in air laden with biomass burning aerosol (BBA) in the southeast Atlantic lower free troposphere (FT) and marine boundary layer (MBL) is assessed during three observation periods (September 2016, August 2017, and October 2018) during the NASA ORACLES (ObseRvations of Aerosols above CLouds and their intEractionS) campaign. Significant sources of BBAs over the African continent combined with regional circulation patterns result in BBA-laden air flowing from the continent over the southeast Atlantic in the lower FT, then subsiding onto the semi-permanent stratocumulus cloud deck, and entraining into the MBL. This study is broken into two parts, first analyzing hydrologic histories of the BBA air in the lower FT and then carrying out a similar assessment in the underlying MBL. Both analyses leverage joint measurements of water concentration and its heavy isotope ratio, interpreted in the previously established (q, δD) phase space framework. For the lower-FT analysis, in situ observations (water concentration, water isotope ratios) in the lower FT are combined with satellite and Modern-Era Retrospective analysis for Research and Applications, Version 2 (MERRA-2), global reanalysis data into simple analytical models to constrain hydrologic histories. We find that even simple models are capable of detecting and constraining the primary processes at play, e.g., distinguishing air masses that experienced moist convection and precipitation (likely over the continent) from those that underwent dry convection and turbulent mixing. Regression of the aircraft data onto a simple model of convective detrainment is used to develop a metric of total precipitation for the in situ measurements and then compared to an aerosol metric of black carbon scavenging also derived from the in situ measurements (the ratio of black carbon to carbon monoxide, BC/CO). There is a strong correlation between the two, suggesting black carbon scavenging has been detected and partially quantified, if only in a relative manner. In comparison, weak correlation is found between BC/CO and the total water concentration itself. The above method is expanded to test for entrainment and precipitation influences on BBA concentrations in the MBL. This is more difficult than the FT analysis since signals are subtle and limited by imperfect knowledge of the water and isotope ratios of the entrained air mass at cloud top. For some of the MBLs observed during 2016 and 2018, lower cloud condensation nuclei (CCN) concentrations occur in the sub-cloud layer coincident with isotopic evidence of precipitation, indicating aerosol scavenging, but more complex models are needed to produce definitive conclusions. For the 2017 observation period, with the highest sub-cloud CCN concentrations, there is no connection between precipitation signals and CCN concentrations, likely indicating the importance of different geographic sampling and air mass history in that year. Nonetheless, these findings along with the FT analysis suggest that utilizing isotope ratio signals may be an aid in addressing cloud–aerosol challenges. Especially for the FT case, these findings support the pursuit of more complex models combined with targeted in situ data to constrain BC scavenging coefficients in a manner which can guide model parameterizations, leading to improvements in the accuracy of simulated BC concentrations and lifetimes in climate models.

Modeling Water Isotopes Using a Global Non‐Hydrostatic Model With an Explicit Convection: Comparison With Gridded Data Sets and Site Observations

AbstractIn this study, we developed a global cloud system‐resolving model (GCSRM) incorporating stable water isotopes (NICAM‐WISO). Using a single‐moment cloud microphysics scheme, we applied the new model to conduct a current climate simulation at a horizontal resolution of 56 km. NICAM‐WISO simulated the seasonal means of the atmospheric hydrological cycle, as well as water isotopic ratios of precipitation and vapor. The model captured the general features of precipitation isotope effects and its spatial correlations were comparable to those of other isotope‐incorporated global atmospheric models. The model showed better spatial correlation between simulated and observed values for a fine‐horizontal‐resolution (14 km) simulation compared to coarse‐horizontal‐resolution (56 km) simulation. However, the model had isotopic biases in tropical mid‐troposphere, ocean, and cold continental regions. A comparison of stable water isotopes between the simulation and observations offered clues for improving the model. For example, in the tropical mid‐troposphere, we found a negative bias in the mixing ratio and isotopic ratio of water vapor. Our analysis using satellite retrievals revealed that these underestimations were caused by weak mixing with the boundary layer vapor and low raindrop evaporation with a small evaporation fraction. The underestimations indicated weak shallow convective mixing in the model, inducing negative bias in the mixing ratio and isotopic ratio of the mid‐tropospheric vapor. These biases were also seen in the fine horizontal‐resolution simulation. Furthermore, we conducted several km‐scale atmospheric isotope circulation simulations using NICAM‐WISO. We expect that global‐scale fine‐horizontal‐resolution simulations using isotope‐incorporated GCSRMs will improve our understanding of the atmospheric hydrological cycle.

The seasonal origins and ages of water provisioning streams and trees in a tropical montane cloud forest

Abstract. Determining the sources of water provisioning streams, soils, and vegetation can provide important insights into the water that sustains critical ecosystem functions now and how those functions may be expected to respond given projected changes in the global hydrologic cycle. We developed multi-year time series of water isotope ratios (δ18O and δ2H) based on twice-monthly collections of precipitation, lysimeter, and tree branch xylem waters from a seasonally dry tropical montane cloud forest in the southeastern Andes mountains of Peru. We then used this information to determine indices of the seasonal origins, the young water fractions (Fyw), and the new water fractions (Fnew) of soil, stream, and tree water. There was no evidence for intra-annual variation in the seasonal origins of stream water and lysimeter water from 1 m depth, both of which were predominantly comprised of wet-season precipitation even during the dry seasons. However, branch xylem waters demonstrated an intra-annual shift in seasonal origin: xylem waters were comprised of wet-season precipitation during the wet season and dry-season precipitation during the dry season. The young water fractions of lysimeter (&lt; 15 %) and stream (5 %) waters were lower than the young water fraction (37 %) in branch xylem waters. The new water fraction (an indicator of water ≤ 2 weeks old in this study) was estimated to be 12 % for branch xylem waters, while there was no significant evidence for new water in stream or lysimeter waters from 1 m depth. Our results indicate that the source of water for trees in this system varied seasonally, such that recent precipitation may be more immediately taken up by shallow tree roots. In comparison, the source of water for soils and streams did not vary seasonally, such that precipitation may mix and reside in soils and take longer to transit into the stream. Our insights into the seasonal origins and ages of water in soils, streams, and vegetation in this humid tropical montane cloud forest add to understanding of the mechanisms that govern the partitioning of water moving through different ecosystems.

Relationship between isotope ratios in precipitation and stream water across watersheds of the National Ecological Observation Network

AbstractThe timescales associated with precipitation moving through watersheds reveal processes that are critical to understanding many hydrologic systems. Measurements of environmental stable water isotope ratios (δ2H and δ18O) have been used as tracers to study hydrologic timescales by examining how long it takes for incoming precipitation tracers become stream discharge, yet limited measurements both spatially and temporally have bounded macroscale evaluations so far. In this observation driven study across North American biomes within the National Ecological Observation Network (NEON), we examined δ18O and δ2H stable water isotope in precipitation (δP) and stream water (δQ) at 26 co‐located sites. With an average 54 precipitation samples and 139 stream water samples per site collected over 2014–2022, assessment of local meteoric water lines and local stream water lines showed geographic variation across North America. Taking the ratio of estimated seasonal amplitudes of δP and δQ to calculate young water fractions (Fyw), showed a Fyw range from 1% to 93% with most sites having Fyw below 20%. Calculated mean transit times (MTT) based on a gamma convolution model showed a MTT range from 0.10 to 13.2 years, with half of the sites having MTT estimates lower than 2 years. Significant correlations were found between the Fyw and watershed area, longest flow length, and the longest flow length/slope. Significant correlations were found between MTT and site latitude, longitude, slope, clay fraction, temperature, precipitation magnitude, and precipitation frequency. The significant correlations between water timescale metrics and the environmental characteristics we report share some similarities with those reported in prior studies, demonstrating that these quantities are primarily driven by site or area specific factors. The analysis of isotope data presented here provides important constraints on isotope variation in North American biomes and the timescales of water movement through NEON study sites.

Assessing the activity of mud volcanism using boron isotope ratios in pore water from surface sediments of mud volcanoes off Tanegashima (SW Japan)

Mud volcanoes can cause various geohazards, so it is very important to know their activity level and their distribution. Surface sediments were collected from four submarine mud volcanoes (MVs) off Tanegashima (SW Japan), namely, MV1, MV2, MV3, and MV14. We extracted pore water from the surface sediments and investigated its chemical and isotopic compositions. The sodium (Na) and chloride (Cl-) concentrations decreased and the boron (B) and lithium (Li) concentrations increased with increasing depth, suggesting that some fluids with lower Na and Cl- concentrations and higher B and Li concentrations than seawater were supplied upward from the deep sub-seafloor. The fluid advection velocities estimated from the pore-water profiles differed for each MV, and those of MV3 were the fastest (14 cm/yr) in this study. The estimated equilibrium temperature with clay minerals using Na and Li concentrations were 93-134°C, corresponding to the temperature of environments around 3.7 to 5.3 km below the seafloor. This indicates that these components originated from these depths and that the origin depth did not reach the plate boundary in this area. The B isotope ratio in the pore water was extremely high up to +57 ‰, suggesting that it was strongly affected by adsorption onto the surface of the sediments. A higher B isotope ratio (+57 ‰) was detected in MV3, which was considered to be more active, indicating that more B was adsorbed onto clay minerals supplied from deeper depths.

A novel laser melting sampler for discrete, sub-centimeter depth-resolved analyses of stable water isotopes in ice cores

Abstract We developed a novel laser melting sampler (LMS) for ice cores to measure the stable water isotope ratios (δ18O and δD) as temperature proxies at sub-centimeter depth resolutions. In this LMS system, a 2 mm diameter movable evacuation nozzle holds an optical fiber through which a laser beam irradiates the ice core. The movable nozzle intrudes into the ice core, the laser radiation meanwhile melts the ice cylindrically, and the meltwater is pumped away simultaneously through the same nozzle and transferred to a vial for analysis. To avoid isotopic fractionation of the ice through vaporization, the laser power is adjusted to ensure that the temperature of the meltwater is always kept well below its boiling point. A segment of a Dome Fuji shallow ice core (Antarctica), using the LMS, was then demonstrated to have been discretely sampled with a depth resolution as small as 3 mm: subsequent analysis of δ18O, δD, and deuterium excess (d) was consistent with results obtained by hand segmentation within measurement uncertainties. With system software to control sampling resolution, the LMS will enable us to identify temperature variations that may be detectable only at sub-centimeter resolutions in ice cores.