|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Journal of Experimental Biology, Vol 202, Issue 9 1139-1150, Copyright © 1999 by Company of Biologists
JOURNAL ARTICLES |
SP Leys, GO Mackie and RW Meech
Biology Department, University of Victoria, British Columbia, Canada V8W 2Y2 and Department of Physiology, University Walk, Bristol BS8 1TD, UK. r.meech@bristol.ac.uk.
All-or-none propagated electrical impulses were recorded from the hexactinellid sponge Rhabdocalyptus dawsoni using suction electrodes attached to lumps of aggregated sponge tissue grafted onto the surface of pieces of the same sponge. Impulses were normally evoked by means of externally applied electrical shocks. Recorded externally using an a.c.-coupled amplifier, the electrical event was triphasic and lasted approximately 30 s; integration gave a diphasic waveform. A further integration to give the form of the membrane action potential produced a monophasic signal. Impulses propagated at 0.27+/-0.1 cm s-1 with an absolute refractory period of 29 s and a relative refractory period of approximately 150 s. Concurrent thermistor flow meter recordings confirmed that water flow through the sponge was arrested following the passage of an impulse, presumably as result of the cessation of beating of the flagella in the flagellated chambers. Tactile stimuli also evoked impulses, as did addition of particulate material to the incoming water stream. Impulses continued to propagate through the sponge during arrests, indicating that the conduction and effector systems were independent. Sponges lack nerves, and a variety of evidence indicates that the conducting tissues are the syncytial trabecular reticulum and pinacoderm layers. Na+-deficient solutions had little effect on the action potential, but propagation was blocked by 10 mmol l-1 Co2+, 1 mmol l-1 Mn2+ or 24 micromol l-1 nimodipine. Tetraethylammonium ions at 1-5 mmol l-1 also blocked propagation without prolonging the action potential. Impulse conduction in the sponge is discussed in relation to excitability and conduction in the protozoa and in plants and to non-nervous conduction in more advanced animals.
This article has been cited by other articles:
![]() |
G. R. D. Elliott and S. P. Leys Coordinated contractions effectively expel water from the aquiferous system of a freshwater sponge J. Exp. Biol., November 1, 2007; 210(21): 3736 - 3748. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. K. Jacobs, N. Nakanishi, D. Yuan, A. Camara, S. A. Nichols, and V. Hartenstein Evolution of sensory structures in basal metazoa Integr. Comp. Biol., November 1, 2007; 47(5): 712 - 723. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. M. Haen, B. F. Lang, S. A. Pomponi, and D. V. Lavrov Glass Sponges and Bilaterian Animals Share Derived Mitochondrial Genomic Features: A Common Ancestry or Parallel Evolution? Mol. Biol. Evol., July 1, 2007; 24(7): 1518 - 1527. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Okamura, A. Nishino, Y. Murata, K. Nakajo, H. Iwasaki, Y. Ohtsuka, M. Tanaka-Kunishima, N. Takahashi, Y. Hara, T. Yoshida, et al. Comprehensive analysis of the ascidian genome reveals novel insights into the molecular evolution of ion channel genes Physiol Genomics, August 11, 2005; 22(3): 269 - 282. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Nickel Kinetics and rhythm of body contractions in the sponge Tethya wilhelma (Porifera: Demospongiae) J. Exp. Biol., December 15, 2004; 207(26): 4515 - 4524. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. P. Leys The Significance of Syncytial Tissues for the Position of the Hexactinellida in the Metazoa Integr. Comp. Biol., February 1, 2003; 43(1): 19 - 27. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. P. Leys and B. M. Degnan Cytological Basis of Photoresponsive Behavior in a Sponge Larva Biol. Bull., December 1, 2001; 201(3): 323 - 338. [Abstract] [Full Text] [PDF] |
||||