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冻土水热耦合模型数值求解及结果检验 总被引：1，自引：0，他引：1
首先对作者所建立的基于多孔介质理论的季节冻土水热迁移耦合模型进行数值求解;对模型方程进行修正, 并给出了模型方程中参数的确定方法。然后以长春松原公路段土体为研究对象, 对实际工程中冻结情况下水分迁移的情况进行预测;给定模型边界条件对模型求解, 将结果与野外实际监测结果进行对比。温度变化对比数据表明, 模型可以较好地预测终值情况, 而中间过程的误差较大, 但是趋势基本一致。水分迁移方向及量的对比数据表明, 模型计算结果要小于实测结果, 但是整体上计算结果与实测结果的变化趋势较一致, 且同样是和最终值吻合较好, 误差最小。结果表明, 模型计算结果可较好地模拟参数最终值, 但存在一定误差。 相似文献
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Ronald Schalla David A. Myers Mary Ann Simmons John M. Thomas Antony P. Toste 《Ground Water Monitoring & Remediation》1988,8(3):90-96
Four state-of-the-art ground water sampling systems were analyzed to determine their reliability in providing representative samples of the volatile chlorinated hydrocarbons trichloroethylene (TCE), perchloroethylene (PCE), and 1,1,1-trichloroethane (TCA) from a simulated monitoring well. The sampling systems studied represent four commonly used devices, including a stainless steel and Teflon® piston pump, a Teflon bailer, a Teflon bladder pump, and a PVC air-lift pump.
Controlled laboratory sampling experiments were conducted in a tank and well test chamber designed to approximate field conditions. A well purging and sampling procedure was used in the test apparatus to determine the accuracy and precision of each device for detecting low concentrations of the compounds in ground water. The compounds selected are some of the most ubiquitous hazardous contaminants found in shallow aquifers near hazardous waste sites throughout the United States.
No significant statistical difference was found among the four sampling systems in detecting the compounds. 相似文献
Controlled laboratory sampling experiments were conducted in a tank and well test chamber designed to approximate field conditions. A well purging and sampling procedure was used in the test apparatus to determine the accuracy and precision of each device for detecting low concentrations of the compounds in ground water. The compounds selected are some of the most ubiquitous hazardous contaminants found in shallow aquifers near hazardous waste sites throughout the United States.
No significant statistical difference was found among the four sampling systems in detecting the compounds. 相似文献
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Removal and bioaccumulation of anthropogenic, halogenated transient tracers in an anoxic fjord 总被引：1，自引：0，他引：1
The persistence of the anthropogenic halogenated tracers, CFC-11 (CCl3F), CFC-12 (CCl2F2), CFC-113 (CCl2FCClF2), carbon tetrachloride (CCl4) and methyl chloroform (CH3CCl3) in oxygen-depleted waters was investigated in the anoxic fjord Framvaren in southern Norway. A model for the ventilation of the water in the fjord was created based on tritium and CFC-12 profiles. The results suggest that CFC-12 is stable in this environment, although still affected by particulate scavenging, while the other four halocarbon species shows signs of significant removal in the oxic/anoxic interface. The first-order removal coefficients were calculated to be 0.35, 0.19, 1.23 and 0.31 year−1 for CFC-11, CFC-113, CCl4 and CH3CCl3, respectively. Significant downward flux of halogenated tracers by sinking organic matter is suggested by the model; the tracers are subsequently released to the water column by the remineralisation of the particles. This process acts as a sink of halogenated tracers in the surface waters, whereas it is a source for the deep waters. Our results points to bioaccumulation factors (BF) for the CFC tracers in the order of 4.4–5.4 (log BF), which is 100–600 times those previously reported. This might be of significance to near-shore, semi-enclosed, basins with a high flux of organic matter, but would still have little importance in open ocean basins. 相似文献
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Mauricio da Rocha Fragoso Gabriel Vieira de Carvalho Felipe Lobo Mendes Soares Daiane Gracieli Faller Luiz Paulo de Freitas Assad Raquel Toste Lívia Maria Barbosa Sancho Elisa Nóbrega Passos Carina Stefoni Böck Bruna Reis Luiz Landau Hernan G. Arango Andrew M. Moore 《Ocean Dynamics》2016,66(3):419-434
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L.G. Anderson T. Tanhua G. Björk S. Hjalmarsson E.P. Jones S. Jutterström B. Rudels J.H. Swift I. Wåhlstöm 《Deep Sea Research Part I: Oceanographic Research Papers》2010,57(7):869-879
The Arctic Ocean has wide shelf areas with extensive biological activity including a high primary productivity and an active microbial loop within the surface sediment. This in combination with brine production during sea ice formation result in the decay products exiting from the shelf into the deep basin typically at a depth of about 150 m and over a wide salinity range centered around S ～33. We present data from the Beringia cruise in 2005 along a section in the Canada Basin from the continental margin north of Alaska towards the north and from the International Siberian Shelf Study in 2008 (ISSS-08) to illustrate the impact of these processes. The water rich in decay products, nutrients and dissolved inorganic carbon (DIC), exits the shelf not only from the Chukchi Sea, as has been shown earlier, but also from the East Siberian Sea. The excess of DIC found in the Canada Basin in a depth range of about 50–250 m amounts to 90±40 g C m?2. If this excess is integrated over the whole Canadian Basin the excess equals 320±140×1012 g C. The high DIC concentration layer also has low pH and consequently a low degree of calcium carbonate saturation, with minimum aragonite values of 60% saturation and calcite values just below saturation. The mean age of the waters in the top 300 m was calculated using the transit time distribution method. By applying a future exponential increase of atmospheric CO2 the invasion of anthropogenic carbon into these waters will result in an under-saturated surface water with respect to aragonite by the year 2050, even without any freshening caused by melting sea ice or increased river discharge. 相似文献
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M.-J. Messias A.J. Watson K.I.C. Oliver E. Fogelqvist S. Bacon N. Bergman M. Danielsen E. Jeansson S.R. Olafsdottir T. Tanhua J.R. Ledwell 《Progress in Oceanography》2008,78(1):85-105
In summer 1996, a tracer release experiment using sulphur hexafluoride (SF6) was launched in the intermediate-depth waters of the central Greenland Sea (GS), to study the mixing and ventilation processes in the region and its role in the northern limb of the Atlantic overturning circulation. Here we describe the hydrographic context of the experiment, the methods adopted and the results from the monitoring of the horizontal tracer spread for the 1996-2002 period documented by ∼10 shipboard surveys. The tracer marked “Greenland Sea Arctic Intermediate Water” (GSAIW). This was redistributed in the gyre by variable winter convection penetrating only to mid-depths, reaching at most 1800 m depth during the strongest event observed in 2002.For the first 18 months, the tracer remained mainly in the Greenland Sea. Vigorous horizontal mixing within the Greenland Sea gyre and a tight circulation of the gyre interacting slowly with the other basins under strong topographic influences were identified. We use the tracer distributions to derive the horizontal shear at the scale of the Greenland Sea gyre, and rates of horizontal mixing at ∼10 and ∼300 km scales. Mixing rates at small scale are high, several times those observed at comparable depths at lower latitudes. Horizontal stirring at the sub-gyre scale is mediated by numerous and vigorous eddies. Evidence obtained during the tracer release suggests that these play an important role in mixing water masses to form the intermediate waters of the central Greenland Sea.By year two, the tracer had entered the surrounding current systems at intermediate depths and small concentrations were in proximity to the overflows into the North Atlantic. After 3 years, the tracer had spread over the Nordic Seas basins. Finally by year six, an intensive large survey provided an overall synoptic documentation of the spreading of the tagged GSAIW in the Nordic Seas. A circulation scheme of the tagged water originating from the centre of the GS is deduced from the horizontal spread of the tracer. We present this circulation and evaluate the transport budgets of the tracer between the GS and the surroundings basins. The overall residence time for the tagged GSAIW in the Greenland Sea was about 2.5 years. We infer an export of intermediate water of GSAIW from the GS of 1 to 1.85 Sv (1 Sv = 106 m3 s−1) for the period from September 1998 to June 2002 based on the evolution of the amount of tracer leaving the GS gyre. There is strong exchange between the Greenland Sea and Arctic Ocean via Fram Strait, but the contribution of the Greenland Sea to the Denmark Strait and Iceland Scotland overflows is modest, probably not exceeding 6% during the period under study. 相似文献
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