Change of Weight of Marine Animals in Diluted Media

1932 ◽  
Vol 9 (1) ◽  
pp. 61-68
Author(s):  
K. HUKUDA

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.

Since Bottazzi's (1897) first determinations of the osmotic pressure of the body fluids of various marine animals many researches have been performed by other authors, particularly in reference to the permeability of the membranes separating the body from its surroundings. Bottazzi (1897, 1906, 1908, b) investigated individuals belonging to very different groups of animals, and found that the osmotic pressure of the body fluids of marine invertebrates, and of elasmobranchs, is very similar to that of the surroundings, while the osmotic pressure of the blood of teleosts is quite different. Changing the osmotic pressure of the medium, the osmotic pressure of most marine invertebrates, and of elasmobranchs, was shown to change in the same direction (L. Fredericq, 1882, 1904; Quinton, 1897; Dakin, 1908) and to reach, finally, the value of the former. The blood of teleosts is much more independent of the medium, for it shown to change only about 30 percent, in concentration, on transferring the animals from sea water to fresh water or vice versa (Dakin, 1908; Dekhuyzen, 1904: Sumner, 1905); other authors, however (fredericq, 1904: Garrey, 1905) could not field even these variations.


1949 ◽  
Vol 26 (2) ◽  
pp. 182-200
Author(s):  
JAMES D. ROBERTSON

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.


2007 ◽  
Vol 28 (2) ◽  
pp. 277-285 ◽  
Author(s):  
Kate Jackson ◽  
Daniel Brooks

AbstractWe recount here two experiments carried out which suggest the existence of the first described integumentary osmoreceptor of its kind in a vertebrate. Domed pressure receptors, present on the cranial scales of alligators have previously been demonstrated to convey the sensation of "touch" when flattened by pressure. Here we find that morphologically similar domed sensory organs present on the post-cranial scales of crocodylid but not alligatorid crocodilians flatten when exposed to increased osmotic pressure, such as that experienced when swimming in sea water hyper-osmotic to the body fluids. When contact between the integument and the surrounding sea water solution is blocked, crocodiles are found to lose their ability to discriminate salinities. We propose that the flattening of the sensory organ in hyper-osmotic sea water is sensed by the animal as "touch", but interpreted as chemical information about its surroundings.


1939 ◽  
Vol 16 (2) ◽  
pp. 155-177
Author(s):  
J. D. ROBERTSON ◽  
D. A. WEBB

Methods are presented for the estimation of sodium, potassium, calcium, magnesium, chloride and sulphate in sea water and in other solutions, such as the blood and body fluids of marine animals, whose inorganic composition is similar to that of sea water. The estimations may be performed on 1 ml. samples, and the limit of error is about 2%. Sodium is precipitated and weighed as sodium zinc uranyl acetate; potassium is precipitated as potassium silver cobaltinitrite which is titrated with ceric sulphate; calcium is titrated with ceric sulphate after two precipitations as oxalate; magnesium is precipitated with hydroxyquinoline and the precipitate brominated and estimated iodometrically; chloride is treated with silver iodate and the released iodate estimated iodometrically; sulphate is titrated with barium chloride using sodium rhodizonate as indicator.


1954 ◽  
Vol 31 (3) ◽  
pp. 402-423
Author(s):  
WARREN J. GROSS

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.


1930 ◽  
Vol 13 (4) ◽  
pp. 437-444 ◽  
Author(s):  
Albrecht Bethe

The surfaces of all marine invertebrates which have been experimented upon are permeable for water and also for both the salts or their ions which are in solution in their blood and in sea water. The forces which tend to bring the salt content of the blood into equilibrium with the salt content of the surrounding sea water are just as great as the forces which strive to prevent osmotic differences. The skin of these animals, save in the cases where special modifications have arisen, serves only as a protecting barrier preventing the loss of the body colloids.


1939 ◽  
Vol 16 (4) ◽  
pp. 387-397
Author(s):  
JAMES D. ROBERTSON

1. Analyses have been made of the body fluids of Echinus esculentus, and two decapod Crustacea, Homarus vulgaris and Cancer pagurus, before and after dialysis with sea water in which they were living. 2. The composition of the perivisceral fluid of Echinus is identical with that of sea water, complete physico-chemical equilibrium existing between the two fluids. 3. The blood plasmas of Homarus and Cancer are maintained in dynamic equilibrium with sea water. They contain more Na, K and Ca and less Cl, Mg and SO4 than sea water. 4. The antennary gland fluid of Cancer contains less Na, K, Ca and Cl and more Mg and SO4 than the blood plasma. 5. The importance of the antennary glands and the surface membranes in regulating the inorganic composition of the blood is discussed.


1968 ◽  
Vol 48 (2) ◽  
pp. 359-380
Author(s):  
D. W. SUTCLIFFE

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.


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