A Study on the Development of a Public LIFELONG EDUCATION Model for Each Stage of the Life Cycle of Residents of Metropolitan Areas in Korea: Based on the Gyeongnam Metropolitan Case

J-Institute ◽  
2021 ◽  
Vol 6 (3) ◽  
pp. 10-22
Author(s):  
Heungkweun Yang ◽  
Euna Yang ◽  
Nakyoung Choi
2018 ◽  
Vol 23 (4) ◽  
pp. 379-407
Author(s):  
Youn-chul Choi ◽  
Kyung-chul Kim ◽  
Boo-kyung Cho ◽  
Hyun-jung Seo ◽  
Hyun-joo Choi

2019 ◽  
Vol 98 (8) ◽  
pp. 897-902 ◽  
Author(s):  
Viktoria V. Erofeeva ◽  
O. V. Maslennikova

Introduction. Morbidity toxocariasis, second in prevalence geohelminthiasis in Russia, is a serious problem in recent years, especially in metropolitan areas. The involvement of earthworms in the life cycle of toxocarias remains poorly understood. The role of earthworms (paratenic hosts) in the circulation and prevention of toxocariasis is established. The work is aimed at a contribution finding out of earthworms Еisеniа fеtidа (paratenic hosts) in toxocariasis circulation and prevention. Material and methods. Nematodes dehelminthization derived from animals. For the first time in Russian Federation, experiments have been conducted on infestation of earthworms Е. fеtidа with infective eggs Tоxоcаrа cаnis and Tоxоcаrа mystax. Results. In the conducted experiments, possibility is proved of infestation of earthworms Е. fеtidа with infective eggs Т. canis and Т. mystax via earth bacterized with 10000 infective eggs. For the first time migration was proved of ascaridate larvae from intestines to skin-muscular sac of the earthworms. Conclusion. Besides, investigation was conducted aimed at finding out of the period duration of Т. canis and Т. mystax larvae staying in earthworms’ intestines and sinews.


Author(s):  
Betty Ruth Jones ◽  
Steve Chi-Tang Pan

INTRODUCTION: Schistosomiasis has been described as “one of the most devastating diseases of mankind, second only to malaria in its deleterious effects on the social and economic development of populations in many warm areas of the world.” The disease is worldwide and is probably spreading faster and becoming more intense than the overall research efforts designed to provide the basis for countering it. Moreover, there are indications that the development of water resources and the demands for increasing cultivation and food in developing countries may prevent adequate control of the disease and thus the number of infections are increasing.Our knowledge of the basic biology of the parasites causing the disease is far from adequate. Such knowledge is essential if we are to develop a rational approach to the effective control of human schistosomiasis. The miracidium is the first infective stage in the complex life cycle of schistosomes. The future of the entire life cycle depends on the capacity and ability of this organism to locate and enter a suitable snail host for further development, Little is known about the nervous system of the miracidium of Schistosoma mansoni and of other trematodes. Studies indicate that miracidia contain a well developed and complex nervous system that may aid the larvae in locating and entering a susceptible snail host (Wilson, 1970; Brooker, 1972; Chernin, 1974; Pan, 1980; Mehlhorn, 1988; and Jones, 1987-1988).


Author(s):  
Randolph W. Taylor ◽  
Henrie Treadwell

The plasma membrane of the Slime Mold, Physarum polycephalum, process unique morphological distinctions at different stages of the life cycle. Investigations of the plasma membrane of P. polycephalum, particularly, the arrangements of the intramembranous particles has provided useful information concerning possible changes occurring in higher organisms. In this report Freeze-fracture-etched techniques were used to investigate 3 hours post-fusion of the macroplasmodia stage of the P. polycephalum plasma membrane.Microplasmodia of Physarum polycephalum (M3C), axenically maintained, were collected in mid-expotential growth phase by centrifugation. Aliquots of microplasmodia were spread in 3 cm circles with a wide mouth pipette onto sterile filter paper which was supported on a wire screen contained in a petri dish. The cells were starved for 2 hrs at 24°C. After starvation, the cells were feed semidefined medium supplemented with hemin and incubated at 24°C. Three hours after incubation, samples were collected randomly from the petri plates, placed in plancettes and frozen with a propane-nitrogen jet freezer.


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