Excretion of thiosulphate, the main detoxification product of sulphide, by the lugworm arenicola marina L

1999 ◽  
Vol 202 (7) ◽  
pp. 855-866 ◽  
Author(s):  
K. Hauschild ◽  
W.M. Weber ◽  
W. Clauss ◽  
M.K. Grieshaber
Keyword(s):  
Body Wall ◽  
Sea Water ◽  
The Body ◽  
Cell Junctions ◽  
Metabolic Inhibitors ◽  
Coelomic Fluid ◽  
Arenicola Marina ◽  
Double Exponential ◽  
Electrophysiological Measurements ◽  
Double Exponential Function

Thiosulphate, the main sulphide detoxification product, is accumulated in the body fluids of the lugworm Arenicola marina. The aim of this study was to elucidate the fate of thiosulphate. Electrophysiological measurements revealed that the transepithelial resistance of body wall sections was 76+/−34 capomega cm2 (mean +/− s.d., N=14), indicating that the body wall of the lugworm is a leaky tissue in which mainly paracellular transport along cell junctions takes place. The body wall was equally permeable from both sides to thiosulphate, the permeability coefficient of which was 1. 31×10(−)3+/−0.37×10(−)3 cm h-1 (mean +/− s.d., N=30). No evidence was found for a significant contribution of the gills or the nephridia to thiosulphate permeation. Thiosulphate flux followed the concentration gradient, showing a linear correlation (r=0.997) between permeated and supplied (10–100 mmol l-1) thiosulphate. The permeability of thiosulphate was not sensitive to the presence of various metabolic inhibitors, implicating a permeation process independent of membrane proteins and showing that the lugworm does not need to use energy to dispose of the sulphide detoxification product. The present data suggest a passive permeation of thiosulphate across the body wall of A. marina. In live lugworms, thiosulphate levels in the coelomic fluid and body wall tissue decreased slowly and at similar rates during recovery from sulphide exposure. The decline in thiosulphate levels followed a decreasing double-exponential function. Thiosulphate was not further oxidized to sulphite or sulphate but was excreted into the sea water.

scholarly journals Clot Formation in the Sipunculid WormThemiste petricola: A Haemostatic and Immune Cellular Response

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Tomás Lombardo ◽  
Guillermo A. Blanco
Keyword(s):  
Cellular Response ◽  
Body Wall ◽  
Sea Water ◽  
Circulatory System ◽  
The Body ◽  
Clot Formation ◽  
Coelomic Fluid ◽  
Fibrous Scaffold ◽  
Second Stage ◽  
Clot Structure

Clot formation in the sipunculidThemiste petricola, a coelomate nonsegmented marine worm without a circulatory system, is a cellular response that creates a haemostatic mass upon activation with sea water. The mass with sealing properties is brought about by homotypic aggregation of granular leukocytes present in the coelomic fluid that undergo a rapid process of fusion and cell death forming a homogenous clot or mass. The clot structure appears to be stabilized by abundant F-actin that creates a fibrous scaffold retaining cell-derived components. Since preservation of fluid within the coelom is vital for the worm, clotting contributes to rapidly seal the body wall and entrap pathogens upon injury, creating a matrix where wound healing can take place in a second stage. During formation of the clot, microbes or small particles are entrapped. Phagocytosis of self and non-self particles shed from the clot occurs at the clot neighbourhood, demonstrating that clotting is the initial phase of a well-orchestrated dual haemostatic and immune cellular response.

The Integration of Activity Cycles in the Behaviour of Arenicola Marina L

1951 ◽  
Vol 28 (1) ◽  
pp. 41-50
Author(s):  
G. P. WELLS ◽  
ELINOR B. ALBRECHT
Keyword(s):  
Body Wall ◽  
Sea Water ◽  
Rhythmic Activity ◽  
The Body ◽  
Neuromuscular System ◽  
Arenicola Marina ◽  
Cyclic Behaviour ◽  
Feeding Cycle ◽  
Activity Cycles ◽  
Set Up

1. Lugworms were dissected in such a way that the movements of the following parts could be simultaneously recorded: extrovert, body wall from the anterior three segments, body wall from the branchiate segments, tail. The preparations were set up in sea water and tracings were taken for many hours in each case. The preparations typically settled down to give cyclic behaviour patterns, remarkably similar to those which intact worms exhibit under favourable conditions, and in which two components were conspicuous. 2. The first, and most invariable, component is the feeding cycle (f cycle), of period 6-7 min. This rhythm originates in the oesophagus, and is transmitted to the muscles of the proboscis (where it causes outbursts of vigorous contraction) and body wall (where it causes correlated contractions in the first three segments, but periodic inhibition in the branchiate segments). 3. The second component was seen in two-thirds of the experiments. It consists of bursts of vigorous rhythmic activity in the body wall and tail, and can appear after their connexion with the extrovert has been severed. Under exceptional circumstances (exhaustion of the f cycle) it may spread to the extrovert trace. Its period is generally 20-60 min. It is apparently identical with the irrigation-defaecation cycle (i-d cycle) of intact worms. 4. Neither pacemaker directly affects the rhythm of the other. The integration of the activities which they determine probably depends on variation in the extent to which their influences spread through the neuromuscular system. They appear to compete for territory. If they happen to discharge outbursts simultaneously, the i-d pacemaker dominates over most of the body wall, and the f pacemaker over the proboscis and mouth region.

Ventilatory and metabolic responses to hypoxia and sulphide in the lugworm Arenicola marina (L.)

2000 ◽  
Vol 203 (20) ◽  
pp. 3177-3188 ◽  
Author(s):  
S.E. Wohlgemuth ◽  
A.C. Taylor ◽  
M.K. Grieshaber
Keyword(s):  
Body Wall ◽  
Oxygen Deficiency ◽  
Ventilation Rate ◽  
The Body ◽  
Coelomic Fluid ◽  
Moderate Hypoxia ◽  
Arenicola Marina ◽  
Sulphide Concentration ◽  
Aerobic Energy Metabolism ◽  
Ventilation Rates

We examined the effects of hypoxia and sulphide levels on the ventilatory activity of Arenicola marina and determined whether ventilation compensates for oxygen deficiency and affects the mode of energy provision. A. marina ventilated intermittently, irrespective of ambient P(O2) and sulphide concentration. The ventilation rate was 28.5+/−16 ml h(−1) g(−1) wet mass during normoxia, but increased to 175+/−60% of this value during moderate hypoxia, during which aerobic energy metabolism was maintained. Below a P(O2) of 6.2 kPa, A. marina reduced the ventilated volume to 54+/−16% of the normoxic value and became anaerobic, as indicated by the accumulation of succinate and strombine. Incubation with 27 micromol l(−1) ambient sulphide had no effect on the normoxic and hypoxic ventilation rates or on the P(O2) below which anaerobiosis started (P(cM)). Increased sulphide concentrations reduced the ventilation rate and shifted the P(cM) towards a higher P(O2) below 10.7 kPa. Sulphide diffused into the body and was at least partially detoxified to thiosulphate when oxygen was present. Under normoxia, sulphide accumulated in the body wall tissue and coelomic fluid when ambient sulphide levels exceeded 117 micromol l(−1) and 216 micromol l(−1), respectively. A decrease in P(O2) in the presence of 27 or 117 micromol l(−1) ambient sulphide had no significant effect on sulphide accumulation.

The Ligamentary System and the Segmental Musculature of Nephtys

1960 ◽  
Vol s3-101 (54) ◽  
pp. 149-176
Author(s):  
R. B. CLARK ◽  
M. E. CLARK
Keyword(s):  
Body Wall ◽  
The Body ◽  
Power Stroke ◽  
Coelomic Fluid ◽  
Unusual Structure ◽  
Shock Absorbers ◽  
Proximal Half ◽  
Unique System ◽  
Body Wall Muscles ◽  
The Impact

Nephtys lacks circular body-wall muscles. The chief antagonists of the longitudinal muscles are the dorso-ventral muscles of the intersegmental body-wall. The worm is restrained from widening when either set of muscles contracts by the combined influence of the ligaments, some of the extrinsic parapodial muscles, and possibly, to a limited extent, by the septal muscles. Although the septa are incomplete, they can and do form a barrier to the transmission of coelomic fluid from one segment to the next under certain conditions, particularly during eversion of the proboscis. Swimming is by undulatory movements of the body but the distal part of the parapodia execute a power-stroke produced chiefly by the contraction of the acicular muscles. It is suspected that the extrinsic parapodial muscles, all of which are inserted in the proximal half of the parapodium, serve to anchor the parapodial wall at the insertion of the acicular muscles and help to provide a rigid point of insertion for them. Burrowing is a cyclical process involving the violent eversion of the proboscis which makes a cavity in the sand. The worm is prevented from slipping backwards by the grip the widest segments have on the sides of the burrow. The proboscis is retracted and the worm crawls forward into the cavity it has made. The cycle is then repeated. Nephtys possesses a unique system of elastic ligaments of unusual structure. The anatomy of the system is described. The function of the ligaments appears to be to restrain the body-wall and parapodia from unnecessary and disadvantageous dilatations during changes of body-shape, and to serve as shock-absorbers against the high, transient, fluid pressures in the coelom, which are thought to accompany the impact of the proboscis against the sand when the worm is burrowing. From what is known of its habits, Nephtys is likely to undertake more burrowing than most other polychaetes.

Heat transfer between fish and ambient water

1976 ◽  
Vol 65 (1) ◽  
pp. 131-145 ◽  
Author(s):  
E. D. Stevens ◽  
A. M. Sutterlin
Keyword(s):  
Body Wall ◽  
Sea Water ◽  
The Body ◽  
Direct Transfer ◽  
Major Fraction ◽  
Metabolic Heat ◽  
Sea Raven ◽  
Before And After ◽  
Ventral Aorta ◽  
Hemitripterus Americanus

1. The ability of fish gills to transfer heat was measured by applying a heat pulse to blood in the ventral aorta and measuring it before and after passing through the gills of a teleost, Hemitripterus americanus. 2. 80–90% of heat contained in the blood is lost during passage through the gills. 3. The fraction of heat not lost during passage through the gills is due to direct transfer of heat between the afferent and efferent artery within the gill bar. 4. The major fraction of metabolic heat (70 - 90%) is lost through the body wall and fins of the sea raven in sea water at 5 degrees C; the remainder is lost through the gills.

The Mechanism of Proboscis Movement in Arenicola

1954 ◽  
Vol s3-95 (30) ◽  
pp. 251-270
Author(s):  
G. P. WELLS
Keyword(s):  
Body Fluid ◽  
Body Wall ◽  
The Body ◽  
Stage I ◽  
Stage Iii ◽  
Forward Movement ◽  
Arenicola Marina ◽  
Buccal Mass ◽  
The Difference ◽  
Longitudinal Muscles

The mechanism of proboscis movement is analysed in detail in Arenicola marina L. and A. ecaudata Johnston, and discussed in relation to the properties of the hydrostatic skeleton. Proboscis activity is based on the following cycle of movements in both species. Stage I. The circular muscles of the body-wall and buccal mass contract; the head narrows and lengthens. Stage IIa. The circular muscles of the mouth and buccal mass relax; the gular membrane (or ‘first diaphragm’ of previous authors) contracts; the mouth opens and the buccal mass emerges. Stage IIb. The longitudinal muscles of the buccal mass and body-wall contract; the head shortens and widens and the pharynx emerges. Stage III. As Stage I. The two species differ anatomically and in their hydrostatic relationships. In ecaudata, the forward movement of body-fluid which extrudes and distends the proboscis is largely due to the contraction of the gular membrane and septal pouches. In marina, the essential mechanism is the relaxation of the oral region which allows the general coelomic pressure to extrude the proboscis. The gular membrane of marina contracts as that of ecaudata does, but its anatomy is different and it appears to be a degenerating structure as far as proboscis extrusion is concerned. Withdrawal of the proboscis may occur while the head is still shortening and widening in Stage IIb, or while it is lengthening and narrowing in Stage III. The proboscis is used both in feeding and in burrowing; in the latter case nothing enters through the mouth; the difference is largely caused by variation in the timing of withdrawal relative to the 3-stage cycle.

scholarly journals Estabilidade osmótica dos fluídos celômicos de um pepino do mar (Holothuria grisea) e de uma estrela-do-mar (Asterina stellifera) (Echinodermata) expostos ao ar durante a maré baixa: um estudo de campo

2002 ◽  
Vol 31 ◽  
Author(s):  
DENILTON VIDOLIN ◽  
IVONETE A. SANTOS GOUVEA ◽  
CAROLINA A. FREIRE
Keyword(s):  
Body Wall ◽  
Sea Water ◽  
Weather Conditions ◽  
Coelomic Fluid ◽  
Slight Reduction ◽  
Air Exposure ◽  
Water Influx ◽  
Sunny Weather ◽  
Wall Permeability ◽  
Water Gain

Animais de entre-marés podem ser expostos ao ar durante a maré baixa, por pelo menos 1-2 horas. Os animais expostos ao ar são susceptíveis a perda de sal e/ou entrada de água durante chuva intensa, ou perda de água pela ação de dessecação do sol. A osmolalidade de amostras de fluido celômico obtidas do pepino-do-mar Holothuria grisea e da estrela-do-mar Asterina stellifera expostas ao ar, ou de animais controles imersos na água do mar adjacente foi determinada. As amostras foram obtidas imediatamente após a exposição ao ar, e novamente após uma hora de exposição ao ar, durante a maré baixa no campo, em tempo nublado, chuvoso, ou ensolarado, na Praia rochosa do Quilombo, Penha, Sul do Brasil. Uma hora de exposição a qualquer das condições climáticas indicadas não alterou a osmolalidade dos fluidos celômicos. Houve pequena redução nas osmolalidades dos fluidos celômicos durante a exposição ao ar com precipitação de chuva. Sugere-se que estes equinodermas possam imediatamente detectar sua exposição ao ar, e possam então reduzir a permeabilidade osmótica de sua parede do corpo, para evitar perda de água para o ar ou entrada de água/saída de sal durante a chuva. ABSTRACT Intertidal animals can be exposed to the air during low tide, for at least 1-2 hours. Animals exposed to the air are subject to salt loss (or water gain) from heavy rains or volume loss from the desiccating action of the sun. Coelomic fluid samples obtained from the sea-cucumber Holothuria grisea and the starfish Asterina stellifera exposed to the air or from control animals submerged in surrounding sea water have been assayed for osmolality. Samples were obtained right after air exposure and again after 1 hour of exposure to the air during low tide in the field, either under cloudy, rainy or sunny weather conditions, in the rocky beach of Quilombo, Penha, Southern Brazil. One hour of exposure to any of the conditions did not change coelomic fluid osmolalities. There was a slight reduction in coelomic fluid osmolalities upon air exposure during rainfall. It is suggested that these echinoderms can somehow immediately detect air exposure and reduce their body wall permeability to avoid water loss or water influx/salt loss during rainfall. RÉSUMÉ Animaux d’entre-marées peuvent êtres exposés a l’air libre pendant le reflux de la marée, pour environ une ou deux heures seulement. Ces animaux, quand exposés a l’air libre, sont susceptibles de perdre du sel et d’absorber de l’eau pendant une période de pluie intense. Par contre, ils peuvent perdre de l’eau si soumis a l’action de dessèchement due a une éxposition au soleil. On a réussi a determiner l’osmolalité d’échantillons du fluide celomique obtenus du Pépin-de-mer Holothuria grisea et de l’Étoile-de-mer Asterina stellifera exposés a l’air libre, e d’animaux-controles immergés dans l’eau de mer voisin. Les échantillons ont été obtenus tout de suite après l’exposition à l’air et, une seconde fois, après une heure d’exposition à l’air libre, pendant la durée de la marée basse, soit sous la pluie, soit au soleil ou soit sous un ciel ombrageux, à la plage rocailleuse de Quilombo, Penha, au sud du Brésil. Une heure d’éxposition à n’importe quelles conditions climatiques indiquées, n’ont pas pu altérer l’osmolalité des fluides celomiques, ce que sugère la conclusion que ces échinodermes peuvent détecter immédiatement sa exposition à l’air libre et peuvent tout de suite réduire la permeabilité osmotique de la membrane que recouvre son corps pour éviter perdre d’eau et, de la même façon, reduire l’absortion de l’eau pendant la pluie. On a observé une petite réduction de fluides celomiques pendant l’exposition a l’air, avec ocurrence de pluie.

Observations in the Skin Pigment and Amoebocytes, and the Occurrence of Phenolases in the Coelomic Fluid of Holothuria Forskali Delle Chiaje

1953 ◽  
Vol 31 (3) ◽  
pp. 529-539 ◽  
Author(s):  
Norman Millott
Keyword(s):  
Body Wall ◽  
Black Body ◽  
The Body ◽  
Coelomic Fluid ◽  
Histological Evidence ◽  
Oxidase System ◽  
Complete Investigation ◽  
Skin Pigment

The black body-wall pigment of Holothuria forskali shows the characteristics of melanin.From histological evidence it appears that the pigment is formed in association with the amoebocytes of the coelomic fluid, which eliminate the pigment in the body wall.The amoebocytes contain a phenolase system, distinct from the cytochromecytochrome oxidase system, with the properties of tyrosinase.The relation of these findings to those of a preceding and more complete investigation into melanogenesis in Diadema is discussed.

scholarly journals The Movements of the Proboscis in Glycera Dibranchiata Ehlers

1937 ◽  
Vol 14 (3) ◽  
pp. 290-301
Author(s):  
G. P. WELLS
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Body Wall ◽  
The Body ◽  
Inhibitory Influence ◽  
Spontaneous Movement ◽  
Arenicola Marina ◽  
Glycera Dibranchiata ◽  
The Central Nervous System ◽  
Nervous Conduction

1. The gut of Glycera consists of (a) the buccal tube, (b) the pharynx, containing the jaws with their associated muscles and glands and the principal stomatogastric ganglia, (c) the oesophagus, leading from the pharynx to (d) the intestine, in which digestion occurs. 2. An "isolated extrovert" preparation is described, consisting of the buccal tube, pharynx and oesophagus. The movements of the buccal tube and oesophagus are recorded separately. The preparation has the following properties: (a) The buccal tube shows vigorous, rapid contractions with a somewhat irregular rhythm. These contractions are due to impulses coming forwards from the pharynx, the buccal tube itself having little power of spontaneous movement. (b) The oesophagus shows tone-waves, on which more rapid contractions of small amplitude may be superposed. These contractions and tone-waves are due to impulses originating in the wall of the oesophagus itself. (c) In a few preparations only, synchronous movements of buccal tube and oesophagus were seen. The site of origin of this synchronous activity was not determined. 3. An "extrovert-body wall" preparation is described, in which the movements of the body wall and buccal tube are separately recorded while the normal nervous conduction paths between them remain intact. The preparation has the following properties: (a) In most cases the body wall shows slight movements only, and the buccal tube moves little or not at all. If, however, the buccal tube be cut across close to the mouth, it begins an irregular rhythm of vigorous contractions, due to impulses originating in the pharynx, which usually continues without diminution for hours. The quiescence of the buccal tube before this cut is made indicates that the central nervous system normally exerts an inhibitory influence on the pharynx. (b) In a few preparations, correlated outbursts of contraction in the body wall and buccal tube were seen. These outbursts, which possibly correspond to extrusion movements of the intact worm, are due to impulses originating in the central nervous system. 4. The results are compared with those previously obtained on Arenicola marina, and reported in an earlier paper.

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