• The Journal of Engineering Geology
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• v.13 no.1
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• pp.51-65
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• 2003

A series of numerical simulations were carried out using STOMP( Subsurface Transport over Multiple Phase) simulator. The flow and distribution of LNAPL were analyzed in homogeneous fine and coarse sand. Vertical movement of LNAPL is faster in the coarser sand. But the total volume of LNAPL retained in the unsaturated zone is larger in the finer sand. A fine layer in the coarse sand domain is also simulated. The results showed that the retained LNAPL volume and shape are highly influenced by the Position of the fine layer. Flow and distributions of LNAPL were simulated when there were heterogeneous lenses in the sand domain. Water table fluctuation was also considered. In these cases, it was found that the heterogeneous lens was a barrier to LNAPL flow, and water table fluctuation stimulated the downward movement of retained LNAPL. The LNAPL flow and distribution observed in these numerical experiments show that in the subsurface environment, the behaviors of LNAPL highly depend on heterogeneities of unsaturated zone and the dynamic hydrogeologic condition such as water table fluctuation. These results can explain some of the complexity of LNAPL flow and distribution Patterns in LNAPL contaminated field sites.

• Parasites, Hosts and Diseases
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• v.23 no.1
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• pp.58-72
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• 1985

A histopathological study was carried out on the duodenum of mice and rats experimentally infected by F. seoulensis. Each mouse was infected with 500 metacercariae and killed after 1, 2, 3 days, 1 and 2 weeks from infection. Each rat was given 1, 000 metacercariae and was examined after 1, 2 and 4 weeks from infection. The duodenal tissue sections of mice and rats were stained with hematoxylin eosin, and PAS stained for the rats of 1 week group. The pathological findings are summarized as below. 1. There were no differences in mucosal findings between the mice and the rats, and between the location of duodenum, 1 and 5 em distal to the pylorus. 2. Each worm embraced a villus exclusively with its foliate fore body which was inserted into the intervillous spaces. The fluke pinched villous epithelia using its oral and ventral suckers. The tribocytic organ destroyed the villous epithelia deeply up to the stroma after 3 days from infection. 3. Apparent villous changes were observed in the mice after 3 days from infection. Villous changes were shortening, widening, blunting or fusion. The villous stroma showed edema, microscopic hemorrhage, capillary congestion, dilatation of lymphatics and inflammatory cell infiltration. The cells were lymphocytes, plasma cells, eosinophils and giant cells. Rarely submucosal and trans:nural inflammation was encountered.