scholarly journals Controls on the water vapor isotopic composition near the surface of tropical oceans and role of boundary layer mixing processes

2019 ◽  
Author(s):  
Camille Risi ◽  
Joseph Galewsky ◽  
Gilles Reverdin ◽  
Florent Brient

Abstract. Understanding what controls the water vapor isotopic composition of the sub-cloud layer (SCL) over tropical oceans (δD0) is a first step towards understanding the water vapor isotopic composition everywhere in the troposphere. We propose an analytical model to predict δD0 as a function of sea surface conditions, humidity and temperature profiles, and the altitude from which the free tropospheric air originates (zorig). To do so, we extend previous studies by (1) prescribing the shape of δD0 vertical profiles, and (2) linking δD0 to zorig. The model relies on the hypotheses that δD0 profiles are steeper than mixing lines and no clouds are precipitating. We show that δD0 does not depend on the intensity of entrainment, dampening hope that δD0 measurements could help constrain this long-searched quantity. Based on an isotope-enabled general circulation model simulation, we show that δD0 variations are mainly controlled by mid-tropospheric depletion and rain evaporation in ascending regions, and by sea surface temperature and zorig in subsiding regions. When the air mixing into the SCL is lower in altitude, it is moister, and thus it depletes more efficiently the SCL. In turn, could δD0 measurements help estimate zorig and thus discriminate between different mixing processes? Estimates that are accurate enough to be useful would be difficult to achieve in practice, requiring measuring daily δD profiles, and measuring δD0 with an accuracy of 0.1 ‰ and 0.4 ‰ in trade-wind cumulus and strato-cumulus clouds respectively.

2019 ◽  
Vol 19 (19) ◽  
pp. 12235-12260 ◽  
Author(s):  
Camille Risi ◽  
Joseph Galewsky ◽  
Gilles Reverdin ◽  
Florent Brient

Abstract. Understanding what controls the water vapor isotopic composition of the sub-cloud layer (SCL) over tropical oceans (δD0) is a first step towards understanding the water vapor isotopic composition everywhere in the troposphere. We propose an analytical model to predict δD0 motivated by the hypothesis that the altitude from which the free tropospheric air originates (zorig) is an important factor: when the air mixing into the SCL is lower in altitude, it is generally moister, and thus it depletes the SCL more efficiently. We extend previous simple box models of the SCL by prescribing the shape of δD vertical profiles as a function of humidity profiles and by accounting for rain evaporation and horizontal advection effects. The model relies on the assumption that δD profiles are steeper than mixing lines, and that the SCL is at steady state, restricting its applications to timescales longer than daily. In the model, δD0 is expressed as a function of zorig, humidity and temperature profiles, surface conditions, a parameter describing the steepness of the δD vertical gradient, and a few parameters describing rain evaporation and horizontal advection effects. We show that δD0 does not depend on the intensity of entrainment, in contrast to several previous studies that had hoped that δD0 measurements could help estimate this quantity. Based on an isotope-enabled general circulation model simulation, we show that δD0 variations are mainly controlled by mid-tropospheric depletion and rain evaporation in ascending regions and by sea surface temperature and zorig in subsiding regions. In turn, could δD0 measurements help estimate zorig and thus discriminate between different mixing processes? For such isotope-based estimates of zorig to be useful, we would need a precision of a few hundred meters in deep convective regions and smaller than 20 m in stratocumulus regions. To reach this target, we would need daily measurements of δD in the mid-troposphere and accurate measurements of δD0 (accuracy down to 0.1 ‰ in the case of stratocumulus clouds, which is currently difficult to obtain). We would also need information on the horizontal distribution of δD to account for horizontal advection effects, and full δD profiles to quantify the uncertainty associated with the assumed shape for δD profiles. Finally, rain evaporation is an issue in all regimes, even in stratocumulus clouds. Innovative techniques would need to be developed to quantify this effect from observations.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Xiaoxin Yang ◽  
Tandong Yao

Abstract This study integrated isotopic composition in precipitation at 50 stations on and around the Tibetan Plateau (TP) and demonstrated the distinct seasonality of isotopic composition in precipitation across the study period. The potential effect of water vapor isotopes on precipitation isotopes is studied by comparing the station precipitation data with extensive isotopic patterns in atmospheric water vapor, revealing the close linkage between the two. The analysis of contemporary water vapor transport and potential helps confirm the different mechanisms behind precipitation isotopic compositions in different areas, as the southern TP is more closely related to large-scale atmospheric circulation such as local Hadley and summer monsoon circulations during other seasons than winter, while the northern TP is subject to the westerly prevalence and advective moisture supply and precipitation processes. The new data presented in this manuscript also enrich the current dataset for the study of precipitation isotopes in this region and together provide a valuable database for verification of the isotope-integrated general circulation model and explanation of related physical processes.


2017 ◽  
Vol 10 (8) ◽  
pp. 3125-3144 ◽  
Author(s):  
Rike Völpel ◽  
André Paul ◽  
Annegret Krandick ◽  
Stefan Mulitza ◽  
Michael Schulz

Abstract. We present the first results of the implementation of stable water isotopes in the Massachusetts Institute of Technology general circulation model (MITgcm). The model is forced with the isotopic content of precipitation and water vapor from an atmospheric general circulation model (NCAR IsoCAM), while the fractionation during evaporation is treated explicitly in the MITgcm. Results of the equilibrium simulation under pre-industrial conditions are compared to observational data and measurements of plankton tow records (the oxygen isotopic composition of planktic foraminiferal calcite). The broad patterns and magnitude of the stable water isotopes in annual mean seawater are well captured in the model, both at the sea surface as well as in the deep ocean. However, the surface water in the Arctic Ocean is not depleted enough, due to the absence of highly depleted precipitation and snowfall. A model–data mismatch is also recognizable in the isotopic composition of the seawater–salinity relationship in midlatitudes that is mainly caused by the coarse grid resolution. Deep-ocean characteristics of the vertical water mass distribution in the Atlantic Ocean closely resemble observational data. The reconstructed δ18Oc at the sea surface shows a good agreement with measurements. However, the model–data fit is weaker when individual species are considered and deviations are most likely attributable to the habitat depth of the foraminifera. Overall, the newly developed stable water isotope package opens wide prospects for long-term simulations in a paleoclimatic context.


2016 ◽  
Vol 29 (24) ◽  
pp. 9125-9139 ◽  
Author(s):  
Adeline Bichet ◽  
Paul J. Kushner ◽  
Lawrence Mudryk

Abstract Better constraining the continental climate response to anthropogenic forcing is essential to improve climate projections. In this study, pattern scaling is used to extract, from observations, the patterned response of sea surface temperature (SST) and sea ice concentration (SICE) to anthropogenically dominated long-term global warming. The SST response pattern includes a warming of the tropical Indian Ocean, the high northern latitudes, and the western boundary currents. The SICE pattern shows seasonal variations of the main locations of sea ice loss. These SST–SICE response patterns are used to drive an ensemble of an atmospheric general circulation model, the National Center for Atmospheric Research (NCAR) Community Atmosphere Model, version 5 (CAM5), over the period 1980–2010 along with a standard AMIP ensemble using observed SST—SICE. The simulations enable attribution of a variety of observed trends of continental climate to global warming. On the one hand, the warming trends observed in all seasons across the entire Northern Hemisphere extratropics result from global warming, as does the snow loss observed over the northern midlatitudes and northwestern Eurasia. On the other hand, 1980–2010 precipitation trends observed in winter over North America and in summer over Africa result from the recent decreasing phase of the Pacific decadal oscillation and the recent increasing phase of the Atlantic multidecadal oscillation, respectively, which are not part of the global warming signal. The method holds promise for near-term decadal climate prediction but as currently framed cannot distinguish regional signals associated with oceanic internal variability from aerosol forcing and other sources of short-term forcing.


2015 ◽  
Vol 15 (10) ◽  
pp. 5537-5555 ◽  
Author(s):  
R. Eichinger ◽  
P. Jöckel ◽  
S. Brinkop ◽  
M. Werner ◽  
S. Lossow

Abstract. This modelling study aims at an improved understanding of the processes that determine the water vapour budget in the stratosphere by means of the investigation of water isotope ratios. An additional (and separate from the actual) hydrological cycle has been introduced into the chemistry–climate model EMAC, including the water isotopologues HDO and H218O and their physical fractionation processes. Additionally an explicit computation of the contribution of methane oxidation to H2O and HDO has been incorporated. The model expansions allow detailed analyses of water vapour and its isotope ratio with respect to deuterium throughout the stratosphere and in the transition region to the troposphere. In order to assure the correct representation of the water isotopologues in the model's hydrological cycle, the expanded system has been evaluated in several steps. The physical fractionation effects have been evaluated by comparison of the simulated isotopic composition of precipitation with measurements from a ground-based network (GNIP) and with the results from the isotopologue-enabled general circulation model ECHAM5-wiso. The model's representation of the chemical HDO precursor CH3D in the stratosphere has been confirmed by a comparison with chemical transport models (1-D, CHEM2D) and measurements from radiosonde flights. Finally, the simulated stratospheric HDO and the isotopic composition of water vapour have been evaluated, with respect to retrievals from three different satellite instruments (MIPAS, ACE-FTS, SMR). Discrepancies in stratospheric water vapour isotope ratios between two of the three satellite retrievals can now partly be explained.


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