Osmotic Responses in the Sipunculid Dendrostomum Zostericolum

1954 ◽  
Vol 31 (3) ◽  
pp. 402-423
Author(s):  
WARREN J. GROSS
Keyword(s):  
Body Weight ◽  
Body Wall ◽  
Sea Water ◽  
Body Fluids ◽  
The Body ◽  
Volume Control ◽  
Active Particles

1. The sipunculid Dendrostomum zostericolum demonstrates no ability to regulate osmotically. 2. Dendrostomum behaves superficially as an osmometer, but is actually more complex: (a) the worm shows volume control in concentrated and dilute sea water; (b) it is permeable to salts, mostly through the gut and/or nephridiopores; (c) it can release osmotically active particles from its body wall to the blood. 3. The body wall of Dendrostomum is highly permeable to water, but only slightly to salts. Permeability for both salts and water is greater inwards than outward. 4. Dendrostomum can tolerate a loss of 36% body weight by desiccation and recover when returned to sea water. The mechanism of this tolerance appears to be the removal by fixation in the tissues, of osmotically active particles from the body fluids.

scholarly journals Adaptation to Changes of Salinity in the Polychaetes

1937 ◽  
Vol 14 (1) ◽  
pp. 56-70
Author(s):  
L. C. BEADLE
Keyword(s):  
Hydrostatic Pressure ◽  
Body Wall ◽  
Sea Water ◽  
Calcium Deficiency ◽  
Body Fluids ◽  
The Body ◽  
Concentration Curve ◽  
Body Volume ◽  
Weight Curve ◽  
Body Wall Muscles

1. Nereis diversicolor collected from the same locality at different times showed smaller weight increases in dilute sea water (25 per cent) during the winter than during the summer months. 2. In spite of great variations in the weight curve, the body fluid concentration curve was very constant. 3. The maintenance of hypertonic body fluids and the regulation of body volume are largely unconnected. 4. The lowering of the weight curve below that theoretically expected from the concentration curve cannot be attributed to passive salt loss through the body surface. It is suggested that this is due to the removal of fluid through the nephridia under the hydrostatic pressure produced by the contraction of the body wall muscles. 5. Animals previously subjected to dilute sea water, when placed in water isotonic with the body fluids, will increase the concentration of the latter. This result is more marked when the internal hydrostatic pressure is high. 6. The results suggest that the osmotic regulatory mechanism involves the removal by the nephridia of fluid hypotonic to the body fluids. But no direct evidence for this is available. 7. Calcium deficiency and cyanide in dilute sea water cause an increase of weight and ultimately inhibit the maintenance of hypertonic body fluids. Both these effects are reversible. 8. The mechanism by which body fluids are maintained hypertonic to the external medium is not sufficiently developed to be of survival value in the locality in which the animals were found. 9. The control of body volume is probably of greater importance. 10. The majority of the extra oxygen consumption in dilute sea water is not the result of osmotic work. It is suggested that it may be due to work done by the body wall muscles in resisting swelling.

Change of Weight of Marine Animals in Diluted Media

1932 ◽  
Vol 9 (1) ◽  
pp. 61-68
Author(s):  
K. HUKUDA
Keyword(s):  
Body Weight ◽  
Osmotic Pressure ◽  
Marine Invertebrates ◽  
Sea Water ◽  
Quantitative Agreement ◽  
Body Fluids ◽  
The Body ◽  
Marine Animals ◽  
Osmotic Swelling

1. Several species of marine invertebrates, and an elasmobranch, have been kept in diluted media. The increase of body weight so caused was compared with the resulting dilution of the body fluids. 2. The bounding membrane of the invertebrates was permeable to salts when the animals were immersed in diluted sea water. 3. The bounding membrane of the elasmobranch was semipermeable, i.e. permeable to water but not to solute. There is a close quantitative agreement between the osmotic swelling observed and the diminution of the osmotic pressure of the blood.

Sodium Regulation and Adaptation to Fresh Water in Gammarid Crustaceans

1968 ◽  
Vol 48 (2) ◽  
pp. 359-380
Author(s):  
D. W. SUTCLIFFE
Keyword(s):  
Body Weight ◽  
Fresh Water ◽  
Body Surface ◽  
Sea Water ◽  
Sodium Concentration ◽  
The Body ◽  
Outward Diffusion ◽  
Gammarus Zaddachi ◽  
Freshwater Habitats ◽  
Sodium Regulation

1. Sodium uptake and loss rates are given for three gammarids acclimatized to media ranging from fresh water to undiluted sea water. 2. In Gammarus zaddachi and G. tigrinus the sodium transporting system at the body surface is half-saturated at an external concentration of about 1 mM/l. and fully saturated at about 10 mM/l. sodium. In Marinogammarus finmarchicus the respective concentrations are six to ten times higher. 3. M. finmarchicus is more permeable to water and salts than G. zaddachi and G. tigrinus. Estimated urine flow rates were equivalent to 6.5% body weight/hr./ osmole gradient at 10°C. in M. finmarchicus and 2.8% body weight/hr./osmole gradient in G. zaddachi. The permeability of the body surface to outward diffusion of sodium was four times higher in M. finmarchicus, but sodium losses across the body surface represent at least 50% of the total losses in both M. finmarchicus and G. zaddachi. 4. Calculations suggest that G. zaddachi produces urine slightly hypotonic to the blood when acclimatized to the range 20% down to 2% sea water. In fresh water the urine sodium concentration is reduced to a very low level. 5. The process of adaptation to fresh water in gammarid crustaceans is illustrated with reference to a series of species from marine, brackish and freshwater habitats.

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 Physiology of the Antennal Gland of Carcinus Maenas (L.)

1969 ◽  
Vol 51 (1) ◽  
pp. 11-16
Author(s):  
R. BINNS
Keyword(s):  
Body Weight ◽  
Sea Water ◽  
Carcinus Maenas ◽  
Urine Flow ◽  
The Body ◽  
Antennal Gland ◽  
Urine Production ◽  
The Mean ◽  
Gland Function ◽  
Water Clearance

1. The space measured by inulin distribution, the ‘inulin volume’, has been determined, and represents approximately 20% of the body weight in crabs ranging in size from 20.0 to 57.2 g. 2. After the injection of labelled inulin into crabs, the increase in activity of the medium is equal to the fall in blood inulin in all dilutions of sea water. Clearance of inulin from the blood is due only to urine production, and therefore the molecule can be used for quantitative investigations of antennal gland function. 3. Urine production in various concentrations of sea water has been determined by measuring the clearance of inulin from the blood and the rates at which the tracer appeared in the external media. By these methods the mean rate of urine production in 100% sea water was estimated to be 4.4% body weight per day. In dilute sea water the rate of urine production increases; for example, in 50% sea water the urine flow is four times greater than in normal sea water.

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 Viscoelasticity of Holothurian Body Wall

1984 ◽  
Vol 109 (1) ◽  
pp. 63-75 ◽  
Author(s):  
TATSUO MOTOKAWA
Keyword(s):  
Mechanical Model ◽  
Body Wall ◽  
Sea Water ◽  
Elastic Stiffness ◽  
Chemical Stimulation ◽  
The Body ◽  
Connective Tissues ◽  
Creep Tests ◽  
Covalent Bonds ◽  
Viscosity Change

1. Stress-relaxation tests and creep tests were performed on the body-wall dermis of two sea cucumbers, Actinopyga echinites (Jäger) and Holothuria leucospilota Brandt. 2. These viscoelastic connective tissues had mechanical properties which agreed well with those of a four-element mechanical model composed of two Maxwell elements connected in parallel. 3. The elastic stiffness of the dermis of Actinopyga was 1.7 MPa and that of Holothuria was 042 MPa. 4. The viscosity of the dermis showed great variation of more than two orders. 5. Chemical stimulation with artificial sea water containing 100 mM potassium increased the viscosity but not elasticity. 6. The viscosity change is suggested to be caused by the change in weak (non-covalent) bonds between macromolecules which constitute the dermis.

scholarly journals Ionic Regulation in Some Marine Invertebrates

1949 ◽  
Vol 26 (2) ◽  
pp. 182-200
Author(s):  
JAMES D. ROBERTSON
Keyword(s):  
Marine Invertebrates ◽  
Sea Water ◽  
Protein Complexes ◽  
Ionic Composition ◽  
Body Fluids ◽  
The Body ◽  
The Other ◽  
Tissue Fluid ◽  
Ionic Regulation ◽  
Decapod Crustacea

1. Analyses have been made of the ionic composition of the body fluids of some twenty marine invertebrates belonging to five phyla. The body fluids were again analysed after dialysis in collodion sacs against samples of the original sea water in which the animals had been kept. Comparison of the two analyses in terms of weight of water gives a true measure of ionic regulation by taking into account such factors as the Donnan equilibrium and the formation of calcium-protein complexes in those animals with significant concentrations of protein in their blood. 2. Some ionic regulation is found in all the animals examined, but it is most pronounced in the cephalopod Mollusca and the decapod Crustacea. 3. The mesogloeal tissue fluid of the jelly-fish Aurelia showed the following composition (expressed as percentage of concentration in the dialysed fluid): Na 99%, K 106%, Ca 96%, Mg 97%, Cl 104%, SO4 47%. This regulation seems to be brought about by elimination of sulphate and accumulation of potassium by the epithelia bounding the mesogloea, with resultant alteration in the remaining ions in conformity with osmotic equilibrium between the jelly and sea water. 4. In the echinoderms studied only potassium is regulated, values in the perivisceral fluid not exceeding 111% being found, with higher values in the ambulacral fluid. Polychaetes regulated potassium (up to 126%) and sometimes reduced sulphate (92%). 5. Regulation extends to all ions in the decapod Crustacea. In six species the range was Na 104-113%, K 77-128%, Ca 108-131%, Mg 14-97% Cl 98-104%, SO4 32-99%. There is a series Lithodes, Cancer, Carcinus, Palinurtis, Nephrops and Homarus in which magnesium falls from 97 to 14%; the series is roughly in accordance with increase of activity. Analyses given of the secretion from the antennary glands emphasize the importance of these organs in controlling the composition of the blood. They eliminate magnesium, sulphate, and sometimes calcium, and conserve the other ions. 6. Lamellibranchs and gastropods accumulate potassium and calcium, and eliminate sulphate to a small degree. Range of values in six species was Na 97-101%, K 107-155%, Ca 103-112%, Mg 97-103%, Cl 99-101%, SO4 87-102%. 7. Considerable ionic regulation exists in the Cephalopoda, ranges being Na 95-98%, K 152-219%, Ca 94-107%, Mg 102-103%, Cl 101-104%, SO4 29-81%. In Eledone and Sepia differential excretion by renal organs is an important factor in this. Sulphate and sodium are eliminated in quantities greater than would be present in an ultrafiltrate of the plasma, tending to lower these values, whereas the other ions are excreted in proportions below those of an ultrafiltrate, tending to elevate their concentrations in the blood. 8. The ratio of equivalents Na+K/Ca+Mg in the body fluids of these marine invertebrates remains at the sea-water figure of 3.8 in Aurelia, echinoderms, anneli worms, and lamellibranchs, but decreases in the gastropods and cephalopods to 3.5. In the decapod Crustacea, owing principally to reduction of magnesium, it increases from 3.8 in Lithodes to 9 and 12 in the Palinura and Astacura genera.

Studies on the Physiology of Ascaris Lumbricoides

1952 ◽  
Vol 29 (1) ◽  
pp. 1-21
Author(s):  
A. D. HOBSON ◽  
W. STEPHENSON ◽  
L. C. BEADLE
Keyword(s):  
Osmotic Pressure ◽  
Body Fluid ◽  
Body Wall ◽  
Sea Water ◽  
External Medium ◽  
Chloride Concentration ◽  
The Body ◽  
Intestinal Fluid ◽  
The Difference ◽  
Saline Medium

1. The total osmotic pressure, electrical conductivity and chloride concentration of the body fluid of Ascaris lumbricoides and of the intestinal contents of the pig have been measured. 2. The results obtained agree with the observations of previous workers that Ascaris normally lives in a hypertonic medium and that it swells or shrinks in saline media which are too dilute or too concentrated. 3. Experiments comparing the behaviour of normal and ligatured animals show that both the body wall and the wall of the alimentary canal are surfaces through which water can pass. 4. 30% sea water has been used as a balanced saline medium for keeping the worms alive in the laboratory. This concentration was selected as being the one in which there was least change in the body weight of the animals exposed to it. 5. The osmotic pressure of the body fluid of worms kept in 30% sea water is approximately the same as in animals taken directly from the pig's intestine. The body fluid of fresh worms is hypertonic to 30% sea water and hypotonic to the intestinal fluid. In 30% sea water the normal osmotic gradient across the body wall is therefore reversed. 6. In 30% sea water the total ionic concentration (as measured by the conductivity) decreases slightly, but the chloride concentration increases by about 50%, although still remaining much below that of the external medium. 7. Experiments in which the animals were allowed to come into equilibrium with various concentrations of sea water from 20 to 40% show that there are corresponding changes in the osmotic pressure of the body fluid which is, however, always slightly above that of the saline medium. The conductivity also changes in a similar manner but is always less than that of the medium, and the difference between the two becomes progressively greater the more concentrated the medium. 8. The chloride concentration of the body fluid varies with but is always below that of the external medium, whether this is intestinal fluid or one of the saline media. In the latter the difference between the internal and external chloride concentrations is least in 20% sea water and becomes progressively greater as the concentration of the medium is increased. 9. Experiments with ligatured worms and with eviscerated cylinders of the body wall show that these share the capacity of the normal worm to maintain the chloride concentration of the body fluid below that of the environment. This power is not possessed by cylinders composed of the cuticle alone. 10. If the worms which have had their internal chloride concentration raised by exposure to 30% sea water are transferred to a medium composed of equal volumes of 30% sea water and isotonic sodium nitrate solution, the chloride concentration of the body fluid is reduced to a value below that of the external medium. This phenomenon is also displayed by worms ligatured after removal from the 30% sea water and, to an even more marked degree, by eviscerated cylinders of the body wall. 11. It is concluded that Ascaris is able to maintain the chloride concentration of the body fluid below that of the external medium by an process of chloride excretion against a concentration gradient, and that this mechanism is resident in the body wall, the cuticle being freely permeable to chloride.

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