Download A century of parasitology: discoveries, ideas, and lessons by John Janovy Jr., Gerald W. Esch PDF

By John Janovy Jr., Gerald W. Esch

ISBN-10: 1118884760

ISBN-13: 9781118884768

Reviews key components in ecological, scientific and molecular parasitology

  • Features essays from the various world's leading parasitologists

 

  • Each subject is determined in context through that includes a key paper from the magazine of Paraistology over the last a hundred years

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Read Online or Download A century of parasitology: discoveries, ideas, and lessons learned by scientists who published in the Journal of Parasitology, 1914-2014 PDF

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Additional info for A century of parasitology: discoveries, ideas, and lessons learned by scientists who published in the Journal of Parasitology, 1914-2014

Sample text

Knipes, and G. Langford. 2007. Gregarina niphandrodes (Eugregarinorida: Septatorina): Oocyst surface architecture. Journal of Parasitology 93: 714–716. ________, J. Detwiler, S. Schwank, M. G. Bolek, A. K. Knipes, and G. J. Langford. 2007. New and emended descriptions of gregarines from flour beetles (Tribolium spp. and Palorus subdepressus: Coleoptera, Tenebrionidae). Journal of Parasitology 93: 1155–1170. Jensen, J. B. 2005. William Trager, 1910–2005. Journal of Parasitology 91: 728. ________, and W.

1970. Recent progress in some aspects of the physiology of parasitic protozoa. Journal of Parasitology 56: 627–633. ________. 1975. On the cultivation of Trypanosoma vivax: a tale of two visits in Nigeria. Journal of Parasitology 61: 2–11. ________. 1976. Prolonged cultivation of malarial parasites (Plasmodium coatneyi and P. falciparum. In Biochemistry of parasites and host-parasite relationships, H. ). Elsevier-North Holland Biomedical Press, Amsterdam, Netherlands, p. 427–434. ________, and J.

5-ml lots are dispensed into 35-mm plastic petri dishes. Culture dishes are placed in a glass desiccator with a stopcock. A candle is placed in the desiccator jar, lighted, and the candle jar is covered. When the flame extinguishes itself, the stopcock is closed. The method produces an inexpensive, predictable, oxygen poor, carbon dioxide enriched atmosphere for erythrocyte culture. Each day the medium is aspirated off, replaced, and the culture is placed in a new candle jar. Thus, the serum supplemented RPMI medium and the culture atmosphere are replaced each day.

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