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Allometric growth of the proglottids and strobila of the tapeworm, Hymenolepis diminuta

Published online by Cambridge University Press:  12 April 2024

P.W. Pappas*
Affiliation:
Department of Evolution, Ecology, and Organismal Biology, The Ohio State University, 1735 Neil Avenue, Columbus, OH, 43210, USA
*
*Fax: 614 292 2030 E-mail: [email protected]
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Abstract

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Hymenolepis diminuta adults were killed and fixed in fully extended positions, and the total lengths of the strobilae, numbers of proglottids, and distances of proglottids along the strobilae were determined. The relationship of proglottid number to distance along the strobila was exponential. Beginning at proglottid 100 (P100), the lengths and widths of proglottids at 100 proglottid intervals were determined, and the surfaces areas were calculated. The relationships of proglottid length and width to proglottid number were linear, but the relationship of proglottid number to surface area (SA) was exponential. The volumes of proglottids were calculated, and the relationship of volume (V) to proglottid number was exponential. The relationship of surface area to volume ratio (SAVR) to proglottid number was exponential; at the anterior end of the worm (P100), the SAVR was 14.6, while at the posterior end of the worm (P1300) the ratio was 4.2. A single exponential equation describing the relationships among proglottid number, SA, and V was derived.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2000

References

Alexander, R.M. (1979) The invertebrates. Cambridge, Cambridge University Press.Google Scholar
Pappas, P.W. (1971) The use of a chrome alum-gelatin (subbing) solution as a general adhesive for paraffin sections. Stain Technology 46, 121124.CrossRefGoogle ScholarPubMed
Pappas, P.W. (1998) Predictability of morphological gradients in the tapeworm, Hymenolepis diminuta . Journal of Helminthology 72, 5557.CrossRefGoogle ScholarPubMed
Pappas, P.W. & Leiby, D.A. (1986) Variation in the sizes of eggs and oncospheres and the numbers and distributions of testes in the tapeworm, Hymenolepis diminuta . Journal of Parasitology 72, 383391.CrossRefGoogle ScholarPubMed
Pappas, P.W., Barley, A.J. & Wardrop, S.M. (1999) Hymenolepis diminuta: glucose and glycogen gradients in the adult tapeworm. Experimental Parasitology 91, 315326.CrossRefGoogle ScholarPubMed
Read, C.P., Rothman, A.H. & Simmons, J.E. (1963) Studies on membrane transport, with special to parasite-host integration. Annals of the New York Academy of Sciences 113, 154205.CrossRefGoogle ScholarPubMed
Roberts, L.S. (1980) Development of Hymenolepis diminuta in its definitive host. pp. 357423 in Arai, H. (Ed.) Biology of the tapeworm, Hymenolepis diminuta. New York, Academic Press.Google Scholar
Threadgold, L.T. & Robinson, A. (1984) Amplification of the cestode surface: a stereological analysis. Parasitology 89, 523535.CrossRefGoogle Scholar