As a supplementary or the only water source in dry regions, dew plays a critical role in the survival of organisms. The new hydrological tracer17O-excess, with almost sole dependence on relative humidity, provides a new way to distinguish the evaporation processes and reconstruct the paleoclimate. Up to now, there is no published daily dew isotope record on δ2H, δ18O, δ17O, d-excess, and17O-excess. Here, we collected daily dew between July 2014 and April 2018 from three distinct climatic regions (i.e., Gobabeb in the central Namib Desert with desert climate, Nice in France with Mediterranean climate, and Indianapolis in the central United States with humid continental climate). The δ2H, δ18O, and δ17O of dew were simultaneously analyzed using a Triple Water Vapor Isotope Analyzer based on Off-Axis Integrated Cavity Output Spectroscopy technique, and then d-excess and17O-excess were calculated. This report presents daily dew isotope dataset under three climatic regions. It is useful for researchers to use it as a reference when studying global dew dynamics and dew formation mechanisms.
Dew is one of the important moisture sources in many arid and semiarid regions. The knowledge of moisture origin of dew under various climatic conditions is still lacking. Isotopic variations can preserve information about moisture origin and formation mechanisms. Therefore, the isotopic compositions of dew and precipitation (δ2H, δ18O, δ17O,
- NSF-PAR ID:
- 10419859
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Hydrological Processes
- Volume:
- 37
- Issue:
- 6
- ISSN:
- 0885-6087
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Abstract -
Abstract The isotopic composition of precipitation is used to trace water cycling and climate change, but interpretations of the environmental information recorded in central Andean precipitation isotope ratios are hindered by a lack of multi‐year records, poor spatial distribution of observations, and a predominant focus on Rayleigh distillation. To better understand isotopic variability in central Andean precipitation, we present a three‐year record of semimonthly δ18Opand δ2Hpvalues from 15 stations in southern Peru and triple oxygen isotope data, expressed as ∆′17Op, from 32 precipitation samples. Consistent with previous work, we find that elevation correlates negatively with δ18Opand that seasonal δ18Opvariations are related to upstream rainout and local convection. Spatial δ18Opvariations and atmospheric back trajectories show that both eastern‐ and western‐derived air masses bring precipitation to southern Peru. Seasonal d‐excesspcycles record moisture recycling and relative humidity at remote moisture sources, and both d‐excesspand ∆′17Opclearly differentiate evaporated and non‐evaporated samples. These results begin to establish the natural range of unevaporated ∆′17Opvalues in the central Andes and set the foundation for future paleoclimate and paleoaltimetry studies in the region. This study highlights the hydrologic understanding that comes from a combination of δ18Op, d‐excessp, and ∆′17Opdata and helps identify the evaporation, recycling, and rainout processes that drive water cycling in the central Andes.
-
Arctic sea-ice loss is emblematic of an amplified Arctic water cycle and has critical feedback implications for global climate. Stable isotopes (δ 18 O, δ 2 H, d-excess ) are valuable tracers for constraining water cycle and climate processes through space and time. Yet, the paucity of well-resolved Arctic isotope data preclude an empirically derived understanding of the hydrologic changes occurring today, in the deep (geologic) past, and in the future. To address this knowledge gap, the Pan-Arctic Precipitation Isotope Network (PAPIN) was established in 2018 to coordinate precipitation sampling at 19 stations across key tundra, subarctic, maritime, and continental climate zones. Here, we present a first assessment of rainfall samples collected in summer 2018 ( n = 281) and combine new isotope and meteorological data with sea ice observations, reanalysis data, and model simulations. Data collectively establish a summer Arctic Meteoric Water Line where δ 2 H = 7.6⋅δ 18 O–1.8 ( r 2 = 0.96, p < 0.01). Mean amount-weighted δ 18 O, δ 2 H, and d-excess values were −12.3, −93.5, and 4.9‰, respectively, with the lowest summer mean δ 18 O value observed in northwest Greenland (−19.9‰) and the highest in Iceland (−7.3‰). Southern Alaska recorded the lowest mean d-excess (−8.2%) and northern Russia the highest (9.9‰). We identify a range of δ 18 O-temperature coefficients from 0.31‰/°C (Alaska) to 0.93‰/°C (Russia). The steepest regression slopes (>0.75‰/°C) were observed at continental sites, while statistically significant temperature relations were generally absent at coastal stations. Model outputs indicate that 68% of the summer precipitating air masses were transported into the Arctic from mid-latitudes and were characterized by relatively high δ 18 O values. Yet 32% of precipitation events, characterized by lower δ 18 O and high d-excess values, derived from northerly air masses transported from the Arctic Ocean and/or its marginal seas, highlighting key emergent oceanic moisture sources as sea ice cover declines. Resolving these processes across broader spatial-temporal scales is an ongoing research priority, and will be key to quantifying the past, present, and future feedbacks of an amplified Arctic water cycle on the global climate system.more » « less
-
Abstract Explosive volcanic eruptions are one of the largest natural climate perturbations, but few observational constraints exist on either the climate responses to eruptions or the properties (size, hemispheric aerosol distribution, etc.) of the eruptions themselves. Paleoclimate records are thus important sources of information on past eruptions, often through the measurement of oxygen isotopic ratios (
δ 18O) in natural archives. However, since many processes affectδ 18O, the dynamical interpretation of these records can be quite complex. Here we present results from new, isotope‐enabled members of the Community Earth System Model Last Millennium Ensemble, documenting eruption‐inducedδ 18O variations throughout the climate system. Eruptions create significant perturbations in theδ 18O of precipitation and soil moisture in central/eastern North America, via excitation of the Atlantic Multidecadal Oscillation. Monsoon Asia and Australia also exhibit strong precipitation and soilδ 18O anomalies; in these cases,δ 18O may reflect changes to El Niño‐Southern Oscillation phase following eruptions. Salinity and seawaterδ 18O patterns demonstrate the importance of both local hydrologic shifts and the phasing of the El Niño‐Southern Oscillation response, both along the equator and in the subtropics. In all cases, the responses are highly sensitive to eruption latitude, which points to the utility of isotopic records in constraining aerosol distribution patterns associated with past eruptions. This is most effective using precipitationδ 18O; all Southern eruptions and the majority (66%) of Northern eruptions can be correctly identified. This work thus serves as a starting point for new, quantitative uses of isotopic records for understanding volcanic impacts on climate. -
Abstract Hydrogen (δD) and oxygen (δ18O) isotopic ratios are strongly correlated in precipitation over time and space, defining the meteoric water line, and the slope of this δD‐δ18O relationship reflects covariations of deuterium excess (d‐excess) with δD or δ18O. This δD‐δ18O line provides a tool for inferring hydrologic processes from the evaporation source to condensation site. Here, we present δD‐δ18O relationships on seasonal and annual timescales for daily precipitation, snow pits, and a 15‐m ice core (Owen) at Summit, Greenland. Seasonally, precipitation δD‐δ18O slopes are less than 8 (summer = 7.70; winter = 7.77), while the annual slope is greater than 8 (8.27). We suggest that intra‐season slopes result primarily from Rayleigh distillation, which, under prevailing conditions, produces slopes less than 8. The summer line has a greater intercept (higher d‐excess) than the winter line. This separation causes annual slopes to be greater than seasonal ones. We attribute high summer d‐excess primarily to contributions of vapor sublimated from the Greenland Ice Sheet and other terrestrial sources. High sublimated moisture proportions result in a large separation between seasonal δD‐δ18O lines, and thus high annual slopes. Inter‐seasonal weighting of precipitation amount also influences annual slopes because slopes are weighed by the number of storms each season. Using snow pit measurements, we demonstrate that precipitation isotopic signals translate to the snowpack. We generate indices to determine Sublimation Proportion Index and Precipitation Weighting Index, and find that annual Owen core δD‐δ18O line slopes are significantly related to these indices, demonstrating that these factors are recorded in ice cores.