Extreme precipitation stable isotopic compositions reveal unexpected summer monsoon incursions in the Qilian Mountains.

Isotope composition and moisture sources of precipitation are important for understanding water cycles and reconstructing paleoclimate. Based on 15-years' precipitation stable Isotope composition (δ18O and δ2H) from four stations of the Qilian Mountains, we found unique δ18O and δ2H features associated with the incursion of the summer monsoon over the Qilian Mountains, northwestern China. In 12 of the 15 years, similar seasonal variations of δ18O and δ2H confirmed a dominant source of moisture from Westerly circulation, and higher intercepts of the local meteoric water line (LMWL) indicated strong recycling of continental moisture. However, in August 2016 and 2018, extremely low slopes and intercepts of the LMWL, and more negative δ18O and δ2H revealed substantial contributions of the Asian summer monsoon to precipitation of the Qilian Mountains, with extremely heavy precipitation in August 2016. The column moisture flux, land-sea thermal contrast, correlations of precipitation δ18O with East Asian Summer Monsoon Index and Westerlies Index, HYSPLIT modeling results and precipitation δ18O along backward trajectories confirmed incursions of the summer monsoon in August 2016 and 2018. Our redefining of the boundary of the summer monsoon region confirmed the summer monsoon incursion zone can extend to the west of longitude 96°E and north of latitude 40°N in strong monsoon years, corresponding to boundaries of monsoon incursions in the mid-Holocene. Temperature correlated with precipitation δ18O at monthly and shorter time scales, but not for whole seasons or at yearly scale, revealing that summer monsoon incursions are therefore more likely than changing temperature to explain the multi-year cycles in the Qilian Mountains ice archives. Continent-scale shifts in atmospheric circulation strongly influence water resources in the Qilian mountains, and may change in frequency as climate warms. This study therefore has important implications for understanding water resources in the Qilian mountains in the past and into the future.

Base flow in the Yarlungzangbo River, Tibet, maintained by the isotopically-depleted precipitation and groundwater discharge.

The extension-induced rift systems on the Tibetan Plateau (TP) may convey large amount of groundwater to rivers, but sources and flow paths of such groundwater are unknown. The Yarlungzangbo River (YR) is the only large river that traverses the southern Tibetan plateau from west to east, following one major suture zone that is cut by extensional normal faults. The faults could influence the flow paths of groundwater discharging to the river. In this study, O and H isotopes, major ions and 222Rn concentrations are analyzed along the YR, and interpreted in relation to structural geology and tectonics. The YR exhibits an abrupt change of isotopic and chemical compositions along with a large increase in flow where the middle reach intersects NE-SW-trending rifts. Low values of δD and δ18O and high concentrations of major ions and 222Rn in the middle reach show that waters are modified isotopically and chemically by a variety of possible water origins, such as recharge of high-altitude glacier melt and discharge from groundwater. Groundwater contributes 27 to 40% of the river flow in the middle reach. Isotopically-light meltwater from high-altitude glacier melt cannot account for the isotope composition of the present outflow of groundwater. The O and H isotope data in the YR and discharging groundwater can be well explained by the groundwater originated as paleo-precipitation during a cooler time, such as the late Pleistocene to early Holocene. The paleo-groundwater discharge can account for about 36 × 108 m3 water budget unbalance in the middle reach. The study provides the first clear isotope evidence for the source of groundwater discharge into a large river through favorable conduits in large-scale active tensile fault zones and confirms the regional scale of groundwater flow on the Tibetan Plateau. Understanding the characteristics and changes of streamflow and surface-groundwater circulation on the Tibetan Plateau will help to manage water resources under a changing environment.

The origin of rare alkali metals in geothermal fluids of southern Tibet, China: A silicon isotope perspective.

Geothermal waters from the Semi, Dagejia and Kawu hot springs in the Shiquanhe-Yarlung Zangbo geothermal field of southern Tibet (China) are highly enriched in rare alkali metals (RAM). However, the enrichment mechanism is still hotly debated. Here, we report the first silicon isotope data of these geothermal waters to unravel the origin of the extreme RAM enrichments. Sinter precipitation in the spring vents and water-rock interaction in the deep reservoir controlled both the silicon budget and silicon isotope fractionation. The rates of water-rock interaction and sinter precipitation in three spring sites decrease in the sequences Semi > Kawu > Dagejia, and Dagejia > Kawu > Semi respectively. Silicon isotope fractionation during sinter precipitation (i.e. Δ30Siprecipitate-solution < -0.1‰) is less than that due to water-rock interaction (i.e. Δ30Sisolution-rocks at least as high as -0.47‰), which makes it possible to use the δ30Si signatures of springs to evaluate the intensity of water-rock interaction. Based on the available evidence, a conceptual model of RAM enrichment is proposed: (i) persistent magmatic activity in southern Tibet provided the initial enrichment of the RAM in host rocks and a heat sources for the deep reservoirs of geothermal systems; (ii) the high Cl- content and long residence time (thousands of years) promote the leaching of RAM from the silicate host rocks.

Adsorption Behavior of Metasilicate on N-Methyl d-Glucamine Functional Groups and Associated Silicon Isotope Fractionation.

Significant isotope fractionation of silicon provides a powerful geochemical tracer for biological and physicochemical processes in terrestrial and marine environments. The exact mechanism involved in silicon uptake as part of the biological process is not well known. The silicon uptake in biological processes is investigated using silicate adsorption onto the N-methylglucamine functional group (sugarlike structure, abbreviated as L) of Amberlite IRA-743 resin as an analogue of the formation of silicate-sugar complexes in plants. This study provides new evidence that certain sugars can react readily with basic silicic acid to form sugar-silicate chelating complexes, and the equilibrium adsorption behavior of silicate can be well described by the Langmuir isotherm with a Gibbs free energy (ΔG) of -11.94 ± 0.21 kJ·mol(-1) at 293 K. The adsorption kinetics corresponds well to a first-order kinetic model in which the adsorption rate constant ka of 1.25 × 10(-4) s(-1) and the desorption rate constant kd of 4.00 × 10(-6) s(-1) are obtained at 293 K. Both ka and kd increase with increasing temperature. The bonding configurations of silicate-sugar complexes imply the principal coordination complex of hexacoordinated silicon (silicon/L = 1:3) in the liquid phase and the dominant tetracoordinated silicon in the solid phase. Similar to those of many natural processes, the biological uptake via the sugar-silicate chelating complexes favors the preferential enrichment of light Si isotopes into solids, and the Rayleigh model controls the dynamic isotope fractionation with an estimated silicon isotope fractionation factor (i.e., αsolid-solution = [Formula: see text]) of 0.9971. This study advanced the fundamental understanding of the dynamic isotope fractionation of silicon during silicon cycling from the lithosphere to the biosphere and hydrosphere in surficial processes.

Identifying recharge from tropical cyclonic storms, Baja California Sur, Mexico.

Groundwater in the Todos Santos watershed in southern Baja California, and throughout the peninsula south of latitude 28°N, has values of (δ18 O‰, δD‰) ranging between (-8.3, -57) and (-10.9, -78). Such negative values are uncharacteristic of the site latitude near the sea level. Altitude effects do not explain the isotope data. Tropical depressions originating along the Pacific coast of North America yield rain with isotopic depletion; rain from these weather systems in southern Arizona commonly has δ18O values<-10‰ in comparison with amount-weighted mean summer and fall rain at -6‰. Isotope data indicate hurricane rain as the predominant source of recharge in southern Baja California, where named tropical depressions bring large rains (>50 mm) at least once every 2 to 3 years, and along the Pacific coast between Jalisco and Oaxaca.

Tracing ground water input to base flow using sulfate (S, O) isotopes.

Sulfate (S and O) isotopes used in conjunction with sulfate concentration provide a tracer for ground water contributions to base flow. They are particularly useful in areas where rock sources of contrasting S isotope character are juxtaposed, where water chemistry or H and O isotopes fail to distinguish water sources, and in arid areas where rain water contributions to base flow are minimal. Sonoita Creek basin in southern Arizona, where evaporite and igneous sources of sulfur are commonly juxtaposed, serves as an example. Base flow in Sonoita Creek is a mixture of three ground water sources: A, basin ground water with sulfate resembling that from Permian evaporite; B, ground water from the Patagonia Mountains; and C, ground water associated with Temporal Gulch. B and C contain sulfate like that of acid rock drainage in the region but differ in sulfate content. Source A contributes 50% to 70%, with the remainder equally divided between B and C during the base flow seasons. The proportion of B generally increases downstream. The proportion of A is greatest under drought conditions.

Geochemical quantification of semiarid mountain recharge.

Analysis of a typical semiarid mountain system recharge (MSR) setting demonstrates that geochemical tracers help resolve the location, rate, and seasonality of recharge as well as ground water flowpaths and residence times. MSR is defined as the recharge at the mountain front that dominates many semiarid basins plus the often-overlooked recharge through the mountain block that may be a significant ground water resource; thus, geochemical measurements that integrate signals from all flowpaths are advantageous. Ground water fluxes determined from carbon-14 ((14)C) age gradients imply MSR rates between 2 x 10(6) and 9 x 10(6) m(3)/year in the Upper San Pedro Basin, Arizona, USA. This estimated range is within an order of magnitude of, but lower than, prior independent estimates. Stable isotopic signatures indicate that MSR has a 65% +/- 25% contribution from winter precipitation and a 35% +/- 25% contribution from summer precipitation. Chloride and stable isotope results confirm that transpiration is the dominant component of evapotranspiration (ET) in the basin with typical loss of more than 90% of precipitation-less runoff to ET. Such geochemical constraints can be used to further refine hydrogeologic models in similar high-elevation relief basins and can provide practical first estimates of MSR rates for basins lacking extensive prior hydrogeologic measurements.