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1.
Areal distributions and complete time histories since 1952 are presented of the tritium and90Sr concentrations in North Atlantic surface water. The distributions are based on a compilation of measured North Atlantic surface water tritium concentrations which is part of this paper and includes hitherto unpublished measurements, and on available90Sr compilations. To reconstruct the insufficiently represented early concentrations, a two-box North Atlantic mixing model with tropospheric input is employed, for which the input is specified (on relative scales), and which is fitted to the available surface water observations. This procedure gives a natural tritium concentration of 0.2 TU (±30%), and furthermore suggests that part of the old oceanic tritium and90Sr measurements are high. The fit requires characteristic model mixing times of 2.5 years (exchange with an intermediate-depth reservoir about three times the size of the surface box) and 30 years (loss into the deep ocean), and a tritium/90Sr input ratio of 310 Ci/Ci. The areal distributions and time histories can serve as boundary value data for evaluations of subsurface tritium and90Sr measurements.  相似文献   

2.
Although the Arctic methane reservoir is large,the emission of methane from the Arctic Ocean into the atmosphere remains poorly constrained.Continuous ship-borne measurements of atmospheric methane near the surface ocean were carried out during two cruises to investigate methane emission from the Arctic Ocean up to the latitude of 87°N.Three-day air mass back trajectories along the cruise tracks indicated that the surface Arctic Ocean could be a potentially important source of methane to the atmosphere.Rapid bursts in methane concentration occurred mainly along the ocean frontal area,suggesting that frontal upwelling in the upper layer of the Arctic Ocean might contribute to methane emissions into the atmosphere.  相似文献   

3.
Seth Rose 《水文研究》1992,6(1):67-78
Environmental tritium was measured in 33 natural water samples representative of precipitation, stream runoff, and groundwater (derived principally from production wells) within the Georgia Piedmont Province. Major ion analyses were used to assist in the interpretation of the tritium results. Tritium concentrations were significantly greater within shallow groundwater derived from the regolith (28–34 TU) and stream runoff (25–30 TU) than within recent rainfall (4–17 TU). Based upon the decay-corrected tritium input function, this probably indicates that at least some of the shallow water is stored within the regolith for a period of approximately 25 years. A ‘post-bomb’ component of recharge was present in all groundwater derived from production wells in the study area. Groundwater sampled from the bedrock aquifers was commonly less tritiated than either stream runoff or shallow water stored in the regolith. the lower tritium concentrations May, have resulted from the mixing of ‘pre-bomb’ water stored within the fractures or the transitional zone directly above the bedrock and modern water stored in the shallow regolith. the preponderance of modern water provides evidence that groundwater flow paths are areally restricted within this setting, probably confined to local surface water drainage basins. the residence time of groundwater in the Piedmont is limited by the lack of deep, gravity-driven regional flow and the localized vertical flow induced by pumping. the results of this study indicate that relatively small tritium concentration variations (10-20 TU) May, have regional hydrological significance in the southeastern Piedmont Province and similar settings.  相似文献   

4.
Future use of tritium in mapping pre-bomb groundwater volumes   总被引：2，自引：0，他引：2  
The tritium input to groundwater, represented as volume-weighted mean tritium concentrations in precipitation, has been close to constant in Tucson and Albuquerque since 1992, and the decrease in tritium concentrations at the tail end of the bomb tritium pulse has ceased. To determine the future usefulness of tritium measurements in southwestern North America, volume-weighted mean tritium levels in seasonal aggregate precipitation samples have been gathered from 26 sites. The averages range from 2 to 9 tritium units (TU). Tritium concentrations increase with site latitude, and possibly with distance from the coast and with site altitude, reflecting local ratios of combination of low-tritium moisture advected from the oceans with high-tritium moisture originating near the tropopause. Tritium used alone as a tool for mapping aquifer volumes containing only pre-bomb recharge to groundwater will become ambiguous when the tritium in precipitation at the end of the bomb tritium pulse decays to levels close to the analytical detection limit. At such a time, tritium in precipitation from the last one to two decades of the bomb pulse will become indistinguishable from pre-bomb recharge. The threshold of ambiguity has already arrived in coastal areas with a mean of 2 TU in precipitation and will follow in the next three decades throughout the study region. Where the mean tritium level is near 5 TU, the threshold will occur between 2025 and 2030, given a detection limit of 0.6 TU. Similar thresholds of ambiguity, with different local timing possible, apply globally.  相似文献   

5.
The Arctic Ocean, the northernmost parts of the earth, covers the total surface area of 14.79 million square kilometers and amounts to only about 4% of global ocean surface area. Although its surface area is the smallest in the four major oceans, the Arct…  相似文献   

6.
Radium-226 (226Ra) activities were measured in the surface water samples collected from the Arctic Ocean and the Bering Sea during the First Chinese National Arctic Research Expedition. The results showed that 226Ra concentrations in the surface water ranged from 0.28 to 1.56 Bq/m3 with an average of 0.76 Bq/m3 in the Arctic Ocean, and from 0.25 to 1.26 Bq/m3 with an average of 0.71 Bq/m3 in the Bering Sea. The values were obviously lower than those from open oceans in middle and low latitudes, indicating that the study area may be partly influenced by sea ice meltwater. In the Bering Sea, 226Ra in the surface water decreased northward, probably as a result of the exchange between the 226Ra-deficient sea ice meltwater and the 226Ra-rich Pacific water. In the Arctic Ocean, 226Ra in the surface water increased northward and eastward. This spatial distribution of 226Ra reflected the variation of the 226Ra-enriched river component in the water mass of the Arctic Ocean. The vertical profiles of 226Ra in the Canadian Basin showed a concentration maximum at 200 m, which could be attributed to the inputs of the Pacific water or/and the bottom shelf water with high 226Ra concentration. This conclusion was consistent with the results from 2H, 18O tracers.  相似文献   

7.
Tritium data in the Dead Sea for the period 1960–1979 are given. Tritium levels have increased until 1965 in the upper layers of the Dead Sea reaching a level of 170 TU, in response to the atmospheric buildup of tritium from thermonuclear testing. The levels have been decreasing ever since, both because of rapidly declining atmospheric concentrations of tritium and because of mixing of the surface layers with tritium deficient, deeper water masses. The depth of penetration of the tracer delineated the depth of meromictic stratification and successfully monitored the deepening of the pycnocline, until the overturn in 1979 homogenised the entire tritium profile. Modelling the changing tritium inventory over this period showed the predominance of the direct exchange across the air/sea interface, both in the buildup of tritium in the lake and also in its subsequent removal from it. The good fit between calculated and measured tritium inventories confirmed the evaporation estimate of 1.46 m/yr (the mean value for the period) with a precision unattained by other methods.  相似文献   

8.
Characteristics of the pCO2 distribution in surface water of the Bering Abyssal Plain and their relationships with the ambient hydrological conditions were discussed using variations of the partial pressure of CO2 in surface water of the Bering Abyssal Plain and the Chukchi Sea. Data in this study are from a field investigation during the First Chinese National Arctic Research Expedition in 1999. Compared to the high productivity in the Bering Continental Shelf, much lower levels of chlorophyll a were observed in the Bering Abyssal Plain. The effect of hydrological factors on the pCO2 distribution in surface seawater of the Plain in summer has become a major driving force and dominated over biological factors. The Plain also presents a High Nutrient Low Chlorophyll (HNLC). In addition, the pCO2 distribution in the Bering Abyssal Plain has also been found to be influenced from the Bering Slope Current which would transform to the Anadyr Current when it inflows northwestward over the Plain. The Anadyr Current would bring a high nutrient water to the western Arctic Ocean where local nutrients are almost depleted in the surface water during the summer time. Resupplying nutrients would stimulate the growth of phytoplankton and enhance capacity of absorbing atmospheric CO2 in the surface water. Otherwise, in the Bering Sea the dissolved inorganic carbon brought from freshwater are not deposited down to the deep sea water but most of them would be transported into the western Arctic Ocean by the Alaska Coastal Current to form a carbon sink there. Therefore, the two carbon sinks in the western Arctic Ocean, one carried by the Anadyr Current and another by the Alaska Costal Current, will implicate the western Arctic Ocean in global change.  相似文献   

9.
The global warming has obviously been causingthe Arctic sea ice shrinking and thinning during thelast 30 years, which would increase free ice waters andenhance biological productivity. These changes willimpact the source and sink of carbon in the ArcticOcean and subarctic waters as well as a feedback tothe global change[1—3]. The Chukchi Sea is located in the southwest ofthe western Arctic Ocean and the Bering Sea in thenorthwest of the North Pacific Ocean. Both seas are 1997—2001) and…  相似文献   

10.
Variation in the concentrations of iodine-129 (129I, T1/2=15.7 Myr), a low-level radioactive component of nuclear fuel waste, is documented in surface waters and depth profiles collected during 2001 along a transect from the Norwegian Coastal Current to the North Pole. The surface waters near the Norwegian coast are found to have 20 times higher 129I concentration than the surface waters of the Arctic Ocean. The depth profiles of 129I taken in the Arctic Ocean reveal a sharp decline in the concentration to a depth of about 300-500 m followed by a weaker gradient extending down to the bottom. A twofold increase in the 129I concentration is observed in the upper 1000 m since 1996. Based on known estimates of marine transient time from the release sources (the nuclear reprocessing facilities at La Hague, France, and Sellafield, UK), a doubling in the 129I inventory of the top 1000 m of the Arctic Ocean is expected to occur between the years 2001 and 2006. As 129I of polar mixed layer and Atlantic layer of the Arctic Ocean is ventilated by the East Greenland Current into the Nordic Seas and North Atlantic Ocean, further dispersal and increase of the isotope concentration in these regions will be encountered in the near future.  相似文献   

11.
The Arctic plays a fundamental role in the climate system and shows significant sensitivity to anthropogenic climate forcing and the ongoing climate change. Accelerated changes in the Arctic are already observed, including elevated air and ocean temperatures, declines of the summer sea ice extent and sea ice thickness influencing the albedo and CO2 exchange, melting of the Greenland Ice Sheet and increased thawing of surrounding permafrost regions. In turn, the hydrological cycle in the high latitude and Arctic is expected to undergo changes although to date it is challenging to accurately quantify this. Moreover, changes in the temperature and salinity of surface waters in the Arctic Ocean and Nordic Seas may also influence the flow of dense water through the Denmark Strait, which are found to be a precursor for changes in the Atlantic meridional overturning circulation with a lead time of around 10 years (Hawkins and Sutton in Geophys Res Lett 35:L11603, 2008). Evidently changes in the Arctic and surrounding seas have far reaching influences on regional and global environment and climate variability, thus emphasizing the need for advanced quantitative understanding of the ocean circulation and transport variability in the high latitude and Arctic Ocean. In this respect, this study combines in situ hydrographical data, surface drifter data and direct current meter measurements, with coupled sea ice–ocean models, radar altimeter data and the latest GOCE-based geoid in order to estimate and assess the quality, usefulness and validity of the new GOCE-derived mean dynamic topography for studies of the ocean circulation and transport estimates in the Nordic Seas and Arctic Ocean.  相似文献   

12.
Radiocarbon data for 11 stations and tritium data for 16 stations in the North Atlantic Ocean from 74°N to 3°N are presented. For radiocarbon, normal errors inΔ14C are± 4‰, and in tritium,± 0.09TU or± 3%, whichever is larger. There is a remarkable, but not simply linear, correlation between oceanic bomb transients in14C and3H. The deep convective mixing in the Greenland Sea is reflected in substantial bomb tracer penetration to all depths, with residence time for the deep, cold core water that seems to be 20 to 30 years. The outflow in the bottom layer southward over the sills of the Denmark Strait and Faroe Passage carries significant tritium concentration, at least to 40°N. Complicated, but coherent, profile structures in the subtropical Atlantic suggest effects of large-scale lateral advection. In particular, a pronounced minimum in both14C and3H might be associated with the Antarctic intermediate water.  相似文献   

13.
The results for three-dimensional (3D) winter and summer tidal flows in the homogeneous Arctic Ocean, obtained with the use of a modified version of the 3D finite-element hydrothermodynamic model QUODDY-4, are presented. It is shown that seasonal variability of the M2 tidal constants (amplitudes and phases of tidal sea surface level elevations) in the Central and Canadian parts of the Arctic Ocean is less than the error in the predicted tidal sea surface level elevations. This means that the seasonal variability can be neglected at least as a first approximation. A different situation is encountered in the Siberian continental shelf, where seasonal changes of tidal amplitude are ±5 cm, while those of tidal phase vary from 15° to several tens of degrees.  相似文献   

14.
Tritium concentrations are used to trace water circulation in the Urumqi and Turfan basins in the Xinjiang, western China. Tritium analyses were made for 77 water samples of river waters, groundwaters, spring waters, lake waters and glacier ice collected in summers in 1992 and 1994. The tritium concentrations in the waters are in a wide range from 0 to 125 TU, most of which are considerably high compared with those of most waters in Japan, because tritium levels in precipitation in the area are over ten times as high as those in Japan. River waters originating in glacier regions contain melt glacier, the proportion of which is over 0.5 to river water. The mean resi-dence time of circulating meteoric water in the mountain regions is estimated to be about 15 years. Most groundwaters and spring waters in the flat regions are mainly derived from river waters originating in glacier regions. The groundwater of greatest tritium concentrations in wells in Urumqi City is derived from Urumqi River about 25 years ago. It takes several ten years for river water to pass the underground to many springs. Some groundwaters and spring waters have taken a long time more than 40 years to travel under the ground. Enrichment of tritium in lake water by evaporation is considered to estimate the contribution of groundwater flow to the recharge of lake. Various contributions of groundwater to lakes are inferred for the various type of salinity in closed or semi-closed lakes. The inflow rates of groundwater to salt lakes are small as against fresh water lakes.  相似文献   

15.
Recent hydrographic data (1981–1982) from the western Canadian Arctic Archipelago and adjacent areas of the Arctic Ocean are interpreted from the viewpoint of thermal energy transfer. Within the Archipelago, a warmer halocline than in the Arctic Ocean and a cooler Atlantic layer are identified. The warmer halocline is a consequence of the continued diffusion of heat from underlying Atlantic water without a significant downward penetration from the surface of cold (≤1.5°C) seawater with salinity increased consequent to ice growth. The cooler Atlantic layer is primarily attributable to an enhanced cooling of these waters in a narrow band over the continental slope and shelf of the southern Beaufort Sea prior to their inflow into the Archipelago. Rates of transport and vertical diffusion in this region are estimated. The significance of these findings in regional and Arctic oceanography is discussed.  相似文献   

16.
Water sampling during the 1993 IV Russian–US Joint Expedition to the Bering and Chukchi Seas (BERPAC) indicates that Pacific Ocean burdens of the long-lived radionuclide 129I are relatively low in the Pacific-influenced Arctic, particularly compared to high latitude waters influenced by the North Atlantic. These low concentrations occur despite the presence of potential submerged anthropogenic sources in the East Sea (Sea of Japan), and in the northwest Pacific Ocean, east of the Kamchatka Peninsula. The concentration of 129I entering the Arctic Ocean through Bering Strait, 0.7×108 atoms kg−1, is only slightly higher than observed in deep Pacific waters. Similar concentrations (0.44–0.76×108 atoms kg−1) measured in Long Strait indicate no significant transfer of 129I eastward into the Chukchi Sea in the Siberian Coastal Current from the Siberian marginal seas to the west. However, the concentrations reported here are more than an order of magnitude higher than the Bering Strait input concentration estimated (1.0×106 atoms kg−1) from bomb fallout mass balances, which supports other existing evidence for a significant atmospheric deposition term for this radionuclide in surface ocean waters. Near-bottom water samples collected in productive waters of the Bering and Chukchi Seas also suggest that sediment regeneration may locally elevate 129I concentrations, and impact its utility as a water mass tracer. As part of this study, two deep 129I profiles were also measured in the East Sea in 1993–1994. The near-surface concentration of 129I ranged from 0.12 to 0.31×108 atoms kg−1. The 129I concentration showed a steady decrease with depth, although because of active deep water ventilation, the entire 3000 m water column exceeded natural concentrations of the radionuclide. Atom ratios of 129I/137Cs in the East Sea also suggest an excess of 129I above bomb fallout estimates, also possibly resulting from atmospheric deposition ultimately originating from nuclear facilities.  相似文献   

17.
Long-term variability of heat content (HC) in the upper 1,000 m of the Arctic Ocean is investigated using surface and subsurface temperature and current data during 1958–2005 compiled by Simple Ocean Data Assimilation. Annual cycle of the Arctic Ocean HC is controlled primarily by the negative and positive excursions in net upper ocean heat flux, while the inter-annual variability is mainly associated with meridional thermal advection from the North Atlantic Ocean. Variability in HC is experienced as a basin-wide cooling/warming in association with the Arctic Oscillation on a decadal time scale. In the first three dominant modes of Empirical Orthogonal Function, the maximum amplitude of HC variability occurs in the Greenland–Norwegian Sea and Eurasian Basin. In general, HC showed increasing trend during 1958–2005 indicating continuous warming with regional variations in magnitude.  相似文献   

18.
Regional behaviour of the groundwater flow system in the Cochabamba Valley, Bolivia, is evaluated through the interpretation of tritium (3H) distributions in groundwater samples from wells and springs. In order to interpret groundwater 3H concentrations in Cochabamba Valley, where no historical record of 3H concentrations in rainfall exists, a reconstructed 3H precipitation record is developed. The record of 3H concentrations in precipitation is fairly extensive in the Amazon Basin and this record was extrapolated to the neighbouring Cochabamba Valley. Tritium concentrations in rainfall have been observed to increase under natural conditions with increasing latitude and with increasing distance from the ocean. By considering these trends, a linear relationship for increasing 3H concentration in precipitation is developed, based on data from the Amazon Basin, that realistically predicts regional 3H distributions from the northeast Brazilian coast to Cuzco, Peru. This 3H precipitation record is then extrapolated to the Cochabamba Valley and, after correction for radiogenic decay, is used to interpret trends in groundwater 3H concentrations within the valley.

The groundwater flow system in one of the principal alluvial fans, which serves as an important groundwater resource for the city, is studied in detail. Tritium concentrations drop from approximately 8–10 tritium units (TU) in the recharge area to concentrations below the detection limit of 0.8 TU further out in the valley. Groundwater velocities of approximately 0.3 to 0.9 m d−1 are estimated from distributions of groundwater 3H concentrations along the alluvial fan with the use of the reconstructed precipitation 3H record. Regional characteristics of the groundwater flow system are discussed with respect to future development and protection of the groundwater resources.  相似文献   


19.
It is of major scientific interests to determine the parameters of momentum, heat and vapor exchange in the planetary boundary layer in order to study the effects of ocean-ice-atmosphere interactions and their feedback mechanisms on global climate[1]. Lin…  相似文献   

20.
Mean annual rates of tritium input into the ocean averaged over 5° latitude bands are presented for the major oceans, for the period 1952–1975. The rates are obtained by converting tritium concentrations in marine precipitation into net oceanic tritium input, by means of a hydrological model. The tropospheric tritium pattern is specified on the basis of available observations, and climatological means from the literature are used for the rates of evaporation and precipitation and for the relative humidity in ship's height, that enter the model. Tritium input by water vapor exchange exceeds that by precipitation about three-fold. Tritium input by river runoff and by net tropospheric tritium outflow from the continents is also accounted for. This contribution is small except for the northern Indian Ocean and the North Atlantic.The inputs have hemispheric maxima near 50° latitude. The northern hemisphere inputs were strongly peaked in 1963–1964, whereas temporal changes in the southern hemisphere were much more gradual. By 1972, about 75% of the total oceanic input had been received by the northern ocean. For the Pacific, the computed total input agrees with the actual tritium inventory within the limits of uncertainty (about ±20%). The global tritium inventory is estimated at 1.9 GCi in 1972, which corresponds to an average tritium yield of 0.9 kg tritium per megaton TNT equivalent of nuclear fusion.  相似文献   

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