Maḥazor Ha-Ḥayyim:Life-Cycle Celebration in the Song of the Ashkenazic Synagogue

AJS Review ◽  
2009 ◽  
Vol 33 (2) ◽  
pp. 305-339
Author(s):  
Geoffrey Goldberg

Joyous life-cycle events celebrated by American Ashkenazic Jews, especially those belonging to the more liberal denominations, invariably conclude with the singing of the wordssiman tov u-mazal tov, yehei lanu u-lekhol yisra'eil(May it bring good luck to us and to all Israel). Whether after the long anxious minutes of theberit milah, the struggle of the youngster through the Hebrew text and trope of thehaftarah, the calling up of the bridegroom (and the bride as well in most non-Orthodox synagogues) at anaufruf, or the breaking of the glass at a wedding, the spontaneous singing serves as a catharsis to relieve the built-up tensions of the communal ritual event as well as to express an outpouring of joy.

KIRYOKU ◽  
2019 ◽  
Vol 3 (2) ◽  
pp. 92
Author(s):  
Yuliani Rahmah

(Omamori in Japanese Belief ) Omamori known as one of animisn and pantheism`s tradition. Omamori, which has been known since the Tokugawa period, still exist in modern Japanese society as a talisman. Theres some questions about what and how the shape of this Japanese charm is. By using literature study approach this article will describe the existence of omamori in Japanese beliefs which includes the definition, form and type of omamori. Omamori is spiritual charms, talismans and amulets in the Japanese religious tradition that possess the power to ward off misfortune and procure good luck. They can be made of pieces of wood, patches of cloth, strips of paper or rings of metal, and come in various sizes. There are seven types of omamori which are most  used by Japanese people. That seven types of omamori are used as protective charms for each stage of the human life cycle.


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.


1994 ◽  
Vol 11 (1) ◽  
pp. 47-56
Author(s):  
Virginia C. Day ◽  
Zachary F. Lansdowne ◽  
Richard A Moynihan ◽  
John A. Vitkevich

1978 ◽  
Vol 23 (2) ◽  
pp. 85-86
Author(s):  
BERTRAM J. COHLER
Keyword(s):  

1978 ◽  
Vol 23 (9) ◽  
pp. 697-697
Author(s):  
ALVIN G. BURSTEIN

1991 ◽  
Vol 36 (4) ◽  
pp. 333-333
Author(s):  
Marilyn Shatz
Keyword(s):  

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