scholarly journals A method for recording electrical activity from the body wall nerve nets in sea anemones

1995 ◽  
Vol 198 (3) ◽  
pp. 817-820
Author(s):  
K Cho ◽  
I D McFarlane

Glass microelectrodes were used to record electrical activity from thin rings cut from the column of the sea anemone Calliactis parasitica. This is the first time that pulses have been recorded from the nervous system in the column. Three pulse types were detected, types A, B and C. Type A pulses are probably associated with neurones of the through-conducting nerve net. Type B pulses may be from the endodermal slow conduction system (SS2). Type C pulses have not previously been recorded and are thought to represent activity in a local nerve net. At this stage we cannot positively state whether the recordings are intracellular from endodermal myoepithelial cells or are extracellular from the sub-epithelial region.

1984 ◽  
Vol 108 (1) ◽  
pp. 137-149
Author(s):  
IAN D. MCFARLANE

1. Single shocks to the column sometimes evoke tentacle contractions, ranging from slight movement of a few scattered tentacles to rapid bending or shortening of all the tentacles. Some individuals are more responsive than others. Complex bursts of electrical activity follow single shocks, but only in tentacles that contract. 2. These single shocks excite pulses in two conducting systems - the through-conducting nerve net (TCNN) and the ectodermal slow conduction system (SSI). When a single shock evokes contractions and bursts of electrical activity, these usually follow the SSI pulse, rarely the TCNN pulse. Stimulation of the SSI alone causes tentacle contraction in responsive anemones. 3. Fast tentacle contractions always follow the second of two closelyspaced TCNN pulses: the TCNN shows facilitation (Pantin, 1935a). An SSI pulse, however, does not facilitate subsequent pulses in either the SSI or TCNN. 4. There are two pathways for activation of tentacle contractions. The TCNN pathway is mechano-sensitive and normally requires facilitation. The SSI pathway is mechano- and chemosensitive, only requires a single SSI pulse to evoke contraction, but is very labile. It is proposed that the TCNN and the SSI do not excite the ectodermal muscles directly, but via a multipolar nerve net.


1974 ◽  
Vol 61 (1) ◽  
pp. 129-143
Author(s):  
I. D. MCFARLANE

1. The rhythm of spontaneous nerve-net pulses is reset by intercalated evoked nerve-net pulses. 2. The origin of spontaneous nerve-net pulses can shift during a burst. There seem to be many potential pacemakers, widely distributed throughout the body, but apparently absent from the tentacles. 3. If a spontaneous or evoked pulse in the endodermal slow conduction system (SS 2) occurs during a burst, the nerve-net pulse intervals are increased during a 15-30 sec period following the SS 2 pulse. Additional SS 2 pulses cause a further increase in pulse intervals. 4. Nerve-net bursts are followed by a sequence of muscular contractions. The size of the contraction shown by any muscle group depends on nerve-net pulse number and frequency, the optimum frequency being different for different muscles. It is suggested that the SS 2 pulse action on nerve-net pulse frequency can significantly alter the behavioural output of nerve-net bursts. The SS 2 activity may represent sensory feedback on to the nervous pacemakers.


1987 ◽  
Vol 133 (1) ◽  
pp. 157-168 ◽  
Author(s):  
I. D. McFARLANE ◽  
D. GRAFF ◽  
C. J.P. GRIMMELIKHUIJZEN

In the sea anemone Calliactis parasitica endodermal application of the anthozoan neuropeptide Antho-RFamide (<Glu-Gly-Arg-Phe-amide), at a concentration of 10−6 or 10−7moll−1, caused a long-lasting increase in tone, contraction frequency and contraction amplitude in several slow muscle groups but had no effect on contractions in fast muscles. The effects were investigated further in isolated muscle preparations. Ectodermal application to whole animals had no effect on muscle contractions. Both ectodermal and endodermal application, at 10−7moll−1, raised electrical activity in an ectodermal conduction system, the SSI, but had no effect on an endodermal conduction system, the SS2. Electrical activity in the SS2 was increased by application at 10−6moll−1 to the endoderm but not to the ectoderm. The peptide had no effect on the through-conducting nerve net. It is concluded that contractions evoked by Antho-RFamide may be partly due to neuronal activity, but probably also involve direct excitation of the muscles. The diverse excitatory actions of Antho-RFamide suggest that it may be a neurotransmitter or neuromodulator in sea anemones.


2000 ◽  
Vol 78 (9) ◽  
pp. 1626-1639 ◽  
Author(s):  
G O Mackie ◽  
R C Wyeth

The behaviour of Chelyosoma productum and Corella inflata (Ascidiacea) was studied in normal and deganglionated animals. Chelyosoma productum lived for over a year after deganglionation and the ganglion did not regenerate. Electrophysiological recordings were made from semi-intact preparations. Responses to stimulation and spontaneous activity continued to be transmitted through the body wall and branchial sac after deganglionation. Spread was slow, decremental, and facilitative. Treatment with >10 µg·mL-1 d-tubocurarine abolished all responses, indicating that nerves mediate conduction of excitation after deganglionation. Histological study using cholinesterase histochemistry and immunolabelling with antisera against tubulin and gonadotropin-releasing hormone showed no evidence of a peri pheral nerve net in regions showing conduction, contrary to previous claims. The cell bodies of the motor neurones were found to lie entirely within the ganglion or its major roots. Their terminal branches intermingled to form netlike arrays. Sensory neurons were identified with cell bodies in the periphery, in both the body wall and the branchial sac. Their processes also intermingled in netlike arrays before entering nerves going to the ganglion. It is concluded that the "residual" innervation that survives deganglionation is composed of either interconnected motor nerve terminals, interconnected sensory neurites, or some combination of the two. In re-inventing the nerve net, ascidians show convergent evolution with sea anemones, possibly as an adaptation to a sessile existence.


1991 ◽  
Vol 156 (1) ◽  
pp. 419-431 ◽  
Author(s):  
I. D. McFarlane ◽  
P. A. Anderson ◽  
C. J. Grimmelikhuijzen

Antho-RWamide I (less than Glu-Ser-Leu-Arg-Trp-NH2) and Antho-RWamide II (less than Glu-Gly-Leu-Arg-Trp-NH2), the second and third anthozoan neuropeptides to be identified, both induced slow contractions of several endodermal muscles in four species of sea anemone. In a fifth species, Protanthea simplex, Antho-RWamide II, but not Antho-RWamide I, evoked contractions of body wall muscles. Isolated, trimmed sphincter muscle preparations of Calliactis parasitica contracted at a threshold concentration of 10(−9) mol l-1 Antho-RWamide II. Antho-RWamide II was more potent than Antho-RWamide I. Unlike the responses to Antho-RFamide (the first anthozoan neuropeptide described), these were simple contractions with no change in spontaneous activity. The Antho-RWamides did not excite electrical activity in any of the three known conducting systems (the through-conducting nerve net and the slow systems 1 and 2), indicating that they may be acting directly on endodermal muscles. Application of peptides to smooth muscle cells, isolated from the sphincter of C. parasitica, confirmed that Antho-RWamide I and II act directly on the muscle. We conclude that the Antho-RWamides may be neurotransmitters at some neuromuscular synapses in sea anemones.


Extracellular polythene suction electrodes have been used to record electrical activity in four species of Madreporaria - Dendrogyra cylindrus, Meandrina meandrites, Mussa angulosa and Eusmilia fastigiata . A colonial conduction system, believed to be the nerve net, was found in all species. It conducted without decrement between all polyps. A second colonial system was found in Meandrina, Mussa and Eusmilia . Pulses could be recorded only from tentacles or oral disks though the system could be excited by electrical or mechanical stimuli to any part of the colony. In the tentacles and oral disk, this conduction system had a refractory period of about 60 ms while in the column or interpolyp regions the refractory period was much longer - up to several seconds. The effect of these differences was to limit the frequency of conduction of pulses in this system between polyps. The second system is compared to the s. s. 1 (ectodermal slow conduction system) of the sea anemone Calliactis parasitica . It is the first demonstrated example of a colonial slow conduction system in the Hexacorallia and is similar in properties to a colonial slow conduction system previously described for Pennatula phosphorea (Octocorallia). The slow conduction system may have a rôle during feeding behaviour by promoting expansion of tentacles and the production of mucus.


1969 ◽  
Vol 51 (2) ◽  
pp. 387-396
Author(s):  
I. D. MCFARLANE

1. Electrical activity has been recorded from the sphincter region of Calliactis parasitica during the behavioural sequence in which the anemone detaches from the substrate and attaches to a Buccinum shell. The ectodermal slow-conduction system (SS1) fires repetitively, the majority of observed pulses occurring in the period prior to detachment (a typical example is 25 SS1pulses at an average frequency of 1 pulse/7 sec.). Shell-tentacle contact is essential for stimulation of SS1activity. 2. Mechanical stimulation of the column excites the SS1, and 30 stimuli at a frequency of about one shock/5 sec. give pedal disk detachment. 3. Electrical stimulation of the ectoderm excites the SS1and about 30 stimuli at frequencies between one shock/3 sec. and one shock/9 sec. produce detachment. Detachment and the SS1 have an identical stimulus threshold. It is concluded that detachment is co-ordinated by the SS1.


1962 ◽  
Vol 39 (3) ◽  
pp. 373-386
Author(s):  
R. MCN. ALEXANDER

1. Creep of narcotized Metridium and Calliactis body-wall at constant tensile stress has been studied quantitatively. 2. It was found to be reversible, and seemed to be controlled by the mesogloea. Its course could be represented by equations of the formε(t)= εo+ευ(I-e-t/τ),where the retardation time τ was about 1 hr. for Metridium and many hours for Calliactis. 3. The results can most simply be explained in terms of a cross-linked and a noncross-linked polymeric system, acting in parallel. An explanation in terms of a lattice of inextensible fibres is not satisfactory. 4. The results are discussed in relation to the behaviour of the animals.


Zoosymposia ◽  
2019 ◽  
Vol 15 (1) ◽  
pp. 44-70
Author(s):  
EMERIC GILLET ◽  
BERTRAND LEFEBVRE ◽  
VERONIQUE GARDIEN ◽  
EMILIE STEIMETZ ◽  
CHRISTOPHE DURLET ◽  
...  

Bolboporites is an enigmatic Ordovician cone-shaped fossil, the precise nature and systematic affinities of which have been controversial over almost two centuries. For the first time, a wide range of techniques (CT-scan, SEM, cathodoluminescence, XPL, UV epifluorescence, EBSD, FT-IR and XRF spectrometry) were applied to well-preserved specimens of Bolboporites from Norway and Russia. Our main finding confirms its echinoderm affinities, as shown by its stereomic microstructure and by the first definitive evidence of its monocrystalline nature. Each cone consists in a single, microporous calcitic crystal with a narrow longitudinal internal canal. These results are combined with all previous data on Bolboporites to critically discuss five alternative interpretations of this fossil, namely theca, basal cone, spine, columnal, and holdfast, respectively. The most parsimonious scenario considers Bolboporites as an isolated spine, which was articulated in life by a short biserial appendage to the body wall of an unknown echinoderm, possibly of echinozoan affinities.


1945 ◽  
Vol s2-85 (340) ◽  
pp. 343-389
Author(s):  
KARM NARAYAN BAHL

1. In an earthworm, as in most aquatic invertebrates, urea and ammonia form the main bulk of nitrogenous excretion and there is no trace of uric acid. These excretory products are first formed in the body-wall and gut-wall, pass therefrom into the coelomic fluid and blood, and are thence eliminated to the exterior by the nephridia. In Pheretima urea and ammonia pass out from the nephridia to the exterior either directly through the skin or through the two ends of the gut. 2. Ammonia and urea have been estimated for the first time in the blood, coelomic fluid, and urine of the earthworm. It has been shown that blood is not a mere carrier of oxygen, as Rogers believed, but that it also takes part in carrying urea and ammonia from the body-wall and gut-wall to the nephridia. The blood of the earthworm does not coagulate, indicating absence of fibrinogen. 3. The role of the nephridia in excretion and osmotic regulation has been determined. A comparison of the osmotic pressures of blood, coelomic fluid, and urine shows that the coelomic fluid is hypotonic to the blood, and that urine is markedly hypotonic both to the blood and coelomic fluid. The protein and chloride contents of the blood, coelomic fluid, and urine have been determined with a view to elucidate the differences in their osmotic pressures. It has been found that the urine contains the merest trace of protein, but that the amount of proteins in the blood is about eight times that contained in the plasma of the coelomic fluid. On the contrary, the chloride content of the coelomic fluid-plasma is about 60 per cent, higher than that of the blood-plasma. 4. The part of urine which is excreted from the blood is probably a protein-free filtrate, but the nephridia reabsorb all the proteins passing into them with the coelomic fluid-plasma. Similarly, there is a reabsorption of chlorides on a large scale from the initial nephridial filtrate during its passage through the nephridia. 5. A convenient method has been devised for collecting urine of the earthworm, which has made it possible to collect as much as 25 c.c. of urine in two and a half hours. The rate of excretion of the urine has been determined and it has been found that in an earthworm living in water the outflow of urine in twenty-four hours must be more than 45 per cent, of its body-weight. 6. It seems that an earthworm, when submerged in water, can live like a fresh water animal, and its gut acts as an osmoregulatory organ in addition to the nephridia, but in the soil it lives like a terrestrial animal and the osmo-regulatory function is adequately discharged by the nephridia alone which reabsorb chlorides and proteins, and are also active in the conservation of water. In Pheretima and other earthworms with an enteronephric type of nephridial system, the gut takes a prominent part in reabsorbing the water of the nephridial fluid and conserving water to its maximum extent. 7. The phagocytic section (ciliated middle tube) believed by Schneider to be absent in the nephridia of Pheretima has been shown to be distinctly present; it is also present in the nephridia of Lampito , Eutyphoeus, and Tonoscolex. The brownish yellow granules characteristic of this phagocytic section form a heavy deposit in the septal nephridia of Pheretima posthuma, heavier than that described in Lumbricus. The deposit increases with the age of the earthworm and forms a ‘storage excretory product’. 8. Spectroscopic examination has revealed that these brownish yellow granules, so far believed to be of guanine, are really blood-pigment granules, since a pyridine solution of them shows the two characteristic bands of haemochromogen. With regard to the blood-pigment, the nephridia function as ‘storage kidneys’. 9. The mechanism of nephridial excretion of the earthworm can be analysed into processes of filtration, reabsorption, and chemical transformation. 10. It is probable that the dorsal and ventral phagocytic organs of earthworms are additional excretory organs.


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