|
|
||||||||
The Biological Bulletin, Vol 196, Issue 1 1-17, Copyright © 1999 by Marine Biological Laboratory
PHYSIOLOGY |
S. Dudgeon, A. Wagner, J. R. Vaisnys and L. W. Buss
Department of Biology, California State University, Northridge, California 91330-8303
Time-lapse video microscopy and image analysis algorithms were used to generate high-resolution time series of the length and volume of a single hydrozoan polyp before and after feeding. A polyp of Podocoryne carnea prior to feeding is effectively static in length and volume. At 20{deg}C, feeding elicits 8-millihertz (mHz) oscillations in polyp length and volume. A polyp connected to a colony by a single stolon displayed an abrupt transition from low-amplitude, 8-mHz oscillations to large-amplitude, 6-mHz oscillations at 1.5-2 h after feeding. The transition was preceded by a substantial decrease in polyp volume and increase in length which coincided with the export of food items from the digestive cavity of the polyp into the colonial gastrovascular system. In contrast, 8-mHz oscillations of a polyp isolated from a colony continued for 12.7 h after feeding, at which time particulates from the digestive cavity were exported into the hydrorhiza and a 4-mHz subharmonic became briefly dominant. Regular oscillatory behavior was terminated by regurgitation at comparable intervals post-feeding in coupled and isolated polyps. These observations are compatible with the hypothesis that the presence of nutrients in the digestive cavity induces polyp oscillations and that release of nutrients into the gastrovascular system similarly induces unfed polyps to oscillate, thereby distributing the contents of the fed polyp throughout the colony.
This article has been cited by other articles:
![]() |
N. W. Blackstone and D. M. Bridge Model Systems for Environmental Signaling Integr. Comp. Biol., August 1, 2005; 45(4): 605 - 614. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. W. Blackstone, M. J. Bivins, K. S. Cherry, R. E. Fletcher, and G. C. Geddes Redox signaling in colonial hydroids: many pathways for peroxide J. Exp. Biol., January 15, 2005; 208(2): 383 - 390. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. W. Blackstone Redox signaling in the growth and development of colonial hydroids J. Exp. Biol., February 15, 2003; 206(4): 651 - 658. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. H. Van Winkle and N. W. Blackstone Variation in Growth and Competitive Ability Between Sexually and Clonally Produced Hydroids Biol. Bull., April 1, 2002; 202(2): 156 - 165. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Ponczek and N. W. Blackstone Effect of Cloning Rate on Fitness-Related Traits in Two Marine Hydroids Biol. Bull., August 1, 2001; 201(1): 76 - 83. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. W. Blackstone Redox state, reactive oxygen species and adaptive growth in colonial hydroids J. Exp. Biol., January 6, 2001; 204(11): 1845 - 1853. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Blackstone Redox control in development and evolution: evidence from colonial hydroids J. Exp. Biol., January 12, 1999; 202(24): 3541 - 3553. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |