Klaus Froehlich

Stable isotope composition of precipitation over southeast Asia

Spatial and temporal variability of the stable isotope composition of precipitation in the southeast Asia and western Pacific region is discussed, with emphasis on the China territory, based on the database of the International Atomic Energy Agency/World Meteorological Organization Global Network Isotopes in Precipitation and the available information on the regional climatology and atmospheric circulation patterns. The meteorological and pluviometric regime of southeast Asia is controlled by five different air masses: (1) polar air mass originating in the Arctic, (2) continental air mass originating over central Asia, (3) tropical-maritime air mass originating in the northern Pacific, (4) equatorial-maritime air mass originating in the western equatorial Pacific, and (5) equatorial-maritime air mass originating in the Indian Ocean. The relative importance of different air masses in the course of a given year is modulated by the monsoon activity and the seasonal displacement of the Intertropical Convergence Zone (ITCZ). Gradual rain-out of moist, oceanic air masses moving inland, associated with monsoon circulation, constitutes a powerful mechanism capable of producing large isotopic depletions in rainfall, often completely overshadowing the dependence of δ 18 O and δ 2 H on temperature. For instance, precipitation at Lhasa station (Tibetan Plateau) during rainy period (June-September) is depleted in 18 O by more than 6 ‰ with respect to winter rainfall, despite of 10°C higher surface air temperature in summer. This characteristic isotopic imprint of monsoon activity is seen over large areas of the region. The oceanic air masses forming the two monsoon systems, Pacific and Indian monsoon, differ in their isotope signatures, as demonstrated by the average δ 18 O of rainfall, which in the south of China (Haikou, Hong Kong) is about 2.5‰ more negative than in the Bay of Bengal (Yangoon). Strong seasonal variations of the deuterium excess values in precipitation observed in some areas of the studied region result from a complete reversal of atmospheric circulation over these areas and changing source of atmospheric moisture. High d-excess values observed at Tokyo and Pohang during winter (15-25‰) result from interaction of dry air masses from the northern Asian continent passing the Sea of Japan and the China Sea and picking up moisture under reduced relative humidity. The isotopic composition of precipitation also provides information about the maximum extent of the ITCZ on the continent during summer.

Deuterium and oxygen-18 isotope composition of precipitation and atmospheric moisture

The stable isotopes of oxygen and hydrogen incorporated in the water molecule ( 18 O and 2 H) have become an important tool not only in Isotope Hydrology, routinely applied to study the origin and dynamics of surface and groundwaters, but also in studies related to atmospheric circulation and palaeoclimatic investigations. A proper understanding of the behaviour of these tracers in the water cycle is required for a meaningful use of these tools in any of these disciplines. Our knowledge of the vertical distribution and the factors controlling the stable isotope ratios of oxygen and hydrogen in atmospheric moisture derives from a limited number of observations and vertical profiles in the atmosphere. An international programme jointly operated by the International Atomic Energy Agency (IAEA) and the World Meteorological Organization (WMO), and operational since 1961. has resulted in the development of a dedicated database to monitor isotope ratios in precipitation in more than 500 meteorological stations world-wide. The main features of the spatial and temporal variations of stable isotope ratios of oxygen and hydrogen in precipitation and atmospheric moisture at the global scale are presented based on the analysis of limited data on water vapour, data obtained by the Global Network for Isotopes in Precipitation IGNIP) and the few observations at high latitudes.

Deuterium excess in precipitation of Alpine regions – moisture recycling

The paper evaluates long-term seasonal variations of the deuterium excess (d-excess = δ2H − 8… δ18O) in precipitation of stations located north and south of the main ridge of the Austrian Alps. It demonstrates that sub-cloud evaporation during precipitation and continental moisture recycling are local, respectively, regional processes controlling these variations. In general, sub-cloud evaporation decreases and moisture recycling increases the d-excess. Therefore, evaluation of d-excess variations in terms of moisture recycling, the main aim of this paper, includes determination of the effect of sub-cloud evaporation. Since sub-cloud evaporation is governed by saturation deficit and distance between cloud base and the ground, its effect on the d-excess is expected to be lower at mountain than at lowland/valley stations. To determine quantitatively this difference, we examined long-term seasonal d-excess variations measured at three selected mountain and adjoining valley stations. The altitude differences between mountain and valley stations ranged from 470 to 1665 m. Adapting the ‘falling water drop’ model by Stewart [J. Geophys. Res., 80(9), 1133–1146 (1975).], we estimated that the long-term average of sub-cloud evaporation at the selected mountain stations (altitudes between about 1600 and 2250 m.a.s.l.) is less than 1 % of the precipitation and causes a decrease of the d-excess of less than 2 ‰. For the selected valley stations, the corresponding evaporated fraction is at maximum 7 % and the difference in d-excess ranges up to 8 ‰. The estimated d-excess differences have been used to correct the measured long-term d-excess values at the selected stations. Finally, the corresponding fraction of water vapour has been estimated that recycled by evaporation of surface water including soil water from the ground. For the two mountain stations Patscherkofel and Feuerkogel, which are located north of the main ridge of the Alps, the maximum seasonal change of the corrected d-excess (July/August) has been estimated to be between 5 and 6 ‰, and the corresponding recycled fraction between 2.5–3 % of the local precipitation. It has been found that the estimated recycled fractions are in good agreement with values derived from other approaches.

Isotope studies in the Caspian Sea.

Oceanographic and isotopic investigations in the Caspian Sea and the analyses of the available data on the discharge to the sea and the observed sea level changes suggest that climatically caused changes of river inflow are the major cause of the sea level fluctuations over the last century. Hydrogen-3 and 3H-3He data indicate that the deep basins of the sea are rapidly ventilated, although the hydraulic turnover time of the sea is approximately 200 years. The concentration levels of the anthropogenic radionuclides 90Sr, 137Cs and 239,240Pu in the water column can be explained by global fallout and therefore, at the sampling sites visited, there were no signs of dumping of radioactive wastes. The anthropogenic radionuclide data support the idea of fast exchange of water masses in the Caspian Sea. The isotopic and oceanographic data collected during the cruises have shown potential to allow for a better understanding of the water circulation in the Caspian Sea.

Lower Groundwater 14C Age by Atmospheric CO2 Uptake During Sampling and Analysis

Uptake of atmospheric CO₂ during sample collection and analysis, and consequent lowering of estimated ages, has rarely been considered in radiocarbon dating of groundwater. Using field and laboratory experiments, we show that atmospheric CO₂ can be easily and rapidly absorbed in hyperalkaline solutions used for the extraction of dissolved inorganic carbon, resulting in elevated ¹⁴C measurements. Kinetic isotope fractionation during atmospheric CO₂ uptake may also result in decrease of δ¹³C, leading to insufficient corrections for addition of dead carbon by geochemical processes. Consequently, measured ¹⁴C values of groundwater should not be used for age estimation without corresponding δ¹³C values, and historical ¹⁴C data in the range of 1 to 10% modern Carbon should be re-evaluated to ensure that samples with atmospheric contamination are recognized appropriately. We recommend that samples for ¹⁴C analysis should be collected and processed in the field and the laboratory without exposure to the atmosphere. These precautions are considered necessary even if ¹⁴C measurements are made with an accelerator mass spectrometer.

Seasonal variation of oxygen-18 in precipitation and surface water of the Poyang Lake Basin, China

Based on the monthly δ18O value measured over a hydrology period in precipitation, runoff of five tributaries and the main lake of the Poyang Lake Basin, combined with hydrological and meteorological data, the characteristics of δ18O in precipitation (δ18OPPT) and runoff (δ18OSUR) are discussed. The δ18OPPT and δ18OSUR values range from−2.75 to−14.12 ‰ (annual mean value=−7.13 ‰ ) and from−2.30 to−8.56 ‰, respectively. The seasonal variation of δ18OPPT is controlled by the air mass circulation in this region, which is dominated by the Asian summer monsoon and the Siberian High during winter. The correlation between the wet seasonal averages of δ18OSUR in runoff of the rivers and δ18OPPT of precipitation at the corresponding stations shows that in the Poyang Lake catchment area the river water consists of 23% direct runoff (precipitation) and 77% base flow (shallow groundwater). This high proportion of groundwater in the river runoff points to the prevalence of wetland conditions in the Poyang Lake catchment during rainy season. Considering the oxygen isotopic composition of the main body of Poyang Lake, no isotopic enrichment relative to river inflow was found during the rainy season with maximum expansion of the lake. Thus, evaporation causing isotopic enrichment is a minor component of the lake water balance in the rainy period. During dry season, a slight isotopic enrichment has been observed, which suggests a certain evaporative loss of lake water in that period.

Distribution of 90Sr, 137Cs and 239,240Pu in Caspian Sea water and biota

Abstract Two sampling expeditions were carried out in the Caspian Sea in 1995 and 1996. The aim was to investigate oceanographic conditions, water dynamics of the Sea and to measure radionuclide concentrations using 90 Sr, 137 Cs and 239,240 Pu as tracers in the water column. Of the three basins comprising the Caspian Sea, the two deep basins (the central and southern basins) appear to be rapidly ventilated on a time scale of about 30 years, as shown by the penetration of radionuclides to bottom waters. The main source of radionuclides in the Sea has been global fallout and subsequent river run-off from catchment areas. At the stations visited, there were no signs of radioactive waste dumping, although the 90 Sr levels found were higher than expected from global fallout, which may be due to remobilization of 90 Sr from soil and its transport by rivers to the Sea. Radionuclide concentrations in fish and caviar are within the expected ranges and are not of radiological importance for consumption of fish and caviar from the Caspian Sea.