Studies on the Physiology of Ascaris Lumbricoides

1952 ◽  
Vol 29 (1) ◽  
pp. 1-21
Author(s):  
A. D. HOBSON ◽  
W. STEPHENSON ◽  
L. C. BEADLE

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.

1952 ◽  
Vol 29 (1) ◽  
pp. 22-29
Author(s):  
A. D. HOBSON ◽  
W. STEPHENSON ◽  
A. EDEN

The results obtained in this investigation are admittedly not as extensive as is desirable but they allow certain conclusions to be drawn. 1. The sodium and potassium contents of the body fluid of Ascaris lumbricoides are somewhat variable, but these variations do not seem to be dependent upon those of the external medium. 2. The calcium and magnesium contents of the body fluid are relatively constant and are not affected by those of the external medium. 3. The chloride concentration of the body fluid is closely related to and always remains lower than that of the external medium. 4. As shown in Table 2, there is a large gap between the total concentrations of inorganic cations and anions in the intestinal fluid of the pig. Presumably a considerable proportion of the inorganic cations are combined with organic anions, at present undetermined. Exposing the worms to saline media composed of chloride caused a large rise in the internal chloride concentration. This may well be a limiting factor in the life of the animals in such media, and the next step forward would seem to be the fuller analysis of the environment to which they are normally exposed.


1954 ◽  
Vol s3-95 (30) ◽  
pp. 251-270
Author(s):  
G. P. WELLS

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.


1936 ◽  
Vol 13 (3) ◽  
pp. 309-328
Author(s):  
L. E. R. PICKEN

1. In Carcinus maenas: (a) The blood may be hypertonic, isotonic or hypotonic to the external medium. (b) The urine may be hypertonic, isotonic or hypotonic to the blood, and its concentration may differ in the two antennary glands. (c) The hydrostatic pressure of the body fluid is c. 13 cm. of water. (d) The colloid osmotic pressure of the blood is c. 11 cm. of water. (e) The urine probably contains protein and has a colloid osmotic pressure of c. 3 cm. of water. 2. In Potamobius fluviatilis: (a) The blood is hypertonic to the external medium. (b) The urine is hypotonic to the blood but hypertonic to the external medium and its concentration may differ in the two antennary glands. (c) The hydrostatic pressure of the body fluid is c. 20 cm. of water. (d) The colloid osmotic pressure of the blood is c. 15 cm. of water. (e) The urine may contain protein and has a colloid osmotic pressure (calculated) of c. 2 cm. of water. 3. In Peripatopsis spp.: (a) The blood is hypertonic to the urine. (b) The hydrostatic pressure of the body fluid is c. 10 cm. of water. (c) The colloid osmotic pressure (calculated) of the blood is c. 5 cm. of water. (d) The urine may contain protein and has a colloid osmotic pressure (calculated) of c. 2.5 cm. of water. 4. It is concluded that filtration is possible and that secretion and resorption almost certainly occur in the formation of the urine. 5. A microthermopile is described. 6. Methods are described for measuring the hydrostatic pressure and the colloid osmotic pressures of the body fluids in small animals.


1948 ◽  
Vol 25 (4) ◽  
pp. 421-436
Author(s):  
J. A. KITCHING

1. On transfer from sea water to dilute sea water, the marine peritrich ciliate Vorticella marina swells more rapidly at higher temperatures. 2. It is concluded that the permeability of the surface of V. marina to water is influenced by temperature, with a Q10 of very roughly 2·5-3·2. 3. The body volume of the fresh-water peritrich ciliate Carchesium aselli is maintained approximately constant when the organism is transferred to solutions of sucrose of concentrations up to about 0·04 M; in higher concentrations the organism shrinks. 4. The rate of output of the contractile vacuole of C. aselli decreases with increasing concentrations of sucrose in the external medium; the rate of output is very low in 0·05 M-sucrose. 5. From a consideration of the effects of sucrose solutions on the body volume and on the rate of vacuolar output it is concluded that the initial osmotic pressure of C. aselli normally exceeds that of the external pond water by about 0·04-0·05 M non-electrolyte. 6. The internal osmotic pressure of C. aselli is not materially increased by increase of temperature. 7. It is concluded that the increase in rate of vacuolar output, which accompanies increase of temperature, counterbalances an increased rate of osmotic uptake of water from the external medium, and that this increased rate of uptake is due to an effect of temperature on the permeability of the surface through which the water enters. 8. The rate of vacuolar output is temporarily much increased when C. aselli, which has been equilibrated in solutions of ethylene glycol, is returned to pond water. 9. It is suggested that the temperature and the osmotic pressure of the external solution largely determine the osmotic stress which is imposed on the organism, and that they thus influence the state of hydration of the protoplasm; in turn this may be supposed to determine the activity of the contractile vacuole.


Author(s):  
N. Kesava Panikkar

1. The brackish-water prawn Palaemonetes varians and the marine prawns Leander serratus and L. squilla are hypotonic in normal sea water, the blood of these species showing osmotic pressures equivalent to 2·3, 2·8 and 2·6 % NaCl respectively, in an external medium of 3·5 % NaCl.2. Palaemonetes varians is isotonic in water of about 2·0 % NaCl and the species is practically homoiosmotic, the difference in its osmotic pressure over a range of 5·0 % NaCl in the external medium being only 0·8–1·0 %. The species has a very wide range of tolerance from water that is nearly fresh to concentrated sea water equivalent to 5·2 % NaCl.3. Leander serratus is much less homoiosmotic than Palaemonetes, and has a limited tolerance to dilution and concentration of the environment. Homoiosmoticity is maintained up to a dilution of 2·5 % in the external medium when isotonicity is reached; but in lower dilutions there is a steady decline in osmotic pressure and the regulatory mechanism evidently breaks down.4. The osmotic behaviour of Leander squilla is very similar to that of L. serratus, but the homoiosmotic behaviour is more marked and it has greater tolerance to dilution of the environment.5. When Leander and Palaemonetes are transferred to very dilute sea water, the internal osmotic pressure falls gradually for about 14–24 hr., varying according to the size of the individual. After the lowest value has been registered there is a slight rise, and a steady state is thereafter maintained.6. Studies on the changes of weight of prawns when transferred to diluted media indicate that the integument (gills) is permeable to water and that, at least in Leander serratus, the amount of water entering is mainly responsible for the dilution of the blood. There is a similar fall in weight when prawns are transferred to concentrated media, due to loss of water.


Author(s):  
R. F. H. Freeman ◽  
T. J. Shuttleworth

Recent studies on the osmotic responses of marine invertebrates to dilution of the external medium have tended to emphasize the osmotic and ionic regulation at the intracellular level rather than at blood/body fluid level. Even in those invertebrates, principally euryhaline crustaceans, possessing osmoregulatory mechanisms which enable them to maintain concentrations of the blood above those of dilute media, the regulation is not perfect, and there is some lowering of the blood concentration below the level exhibited in full-strength sea water (Lockwood, 1962). This requires the establishment of a new osmotic equilibrium between the intracellular solutes and those of the blood. The nature of the intracellular osmotic constituents is, however, strikingly different from those of the blood, even in those invertebrates which are stenohaline and purely marine in their distribution (Robertson, 1961). The osmotic pressure of the blood is due almost entirely to the same inorganic electrolytes as are present in sea water, although the percentage contribution of the various ions may differ. On the other hand these inorganic ions account for only about one third to one half of the intracellular osmotic pressure. The remainder is accounted for by organic solutes, most particularly free amino acids.


1976 ◽  
Vol 65 (1) ◽  
pp. 131-145 ◽  
Author(s):  
E. D. Stevens ◽  
A. M. Sutterlin

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.


1972 ◽  
Vol 57 (3) ◽  
pp. 821-838
Author(s):  
JOHN P. LEADER

1. The larva of Philanisus plebeius is capable of surviving for at least 10 days in external salt concentrations from 90 mM/l sodium chloride (about 15 % sea water) to 900 mM/l sodium chloride (about 150 % sea water). 2. Over this range the osmotic pressure and the sodium and chloride ion concentrations of the haemolymph are strongly regulated. The osmotic pressure of the midgut fluid and rectal fluid is also strongly regulated. 3. The body surface of the larva is highly permeable to water and sodium ions. 4. In sea water the larva is exposed to a large osmotic flow of water outwards across the body surface. This loss is replaced by drinking the medium. 5. The rectal fluid of larvae in sea water, although hyperosmotic to the haemolymph, is hypo-osmotic to the medium, making it necessary to postulate an extra-renal site of salt excretion. 6. Measurements of electrical potential difference across the body wall of the larva suggest that in sea water this tissue actively transports sodium and chloride ions out of the body.


2003 ◽  
Vol 77 (2) ◽  
pp. 167-172 ◽  
Author(s):  
E. Frontera ◽  
F. Serrano ◽  
D. Reina ◽  
M. Alcaide ◽  
J. Sánchez-López ◽  
...  

AbstractAdult Ascaris suum were dissected to obtain different worm components (body wall, body fluid, ovaries, uterus and oesophagus) which were used as antigens when testing 95 sera of naturally A. suum-infected Iberian pigs by enzyme-linked immunosorbent assay (ELISA) and Western blot (WB). Pigs with patent Ascaris infections had significantly lower ELISA optical density values than pigs without adult worms when using the body fluid and the body wall as antigens. A poor negative correlation was found between adult intestinal worm burden or eggs in faeces and specific antibody responses, measured by ELISA and WB using all antigens. By WB, the recognition of specific bands was variable, but three groups of bands with molecular weights of 97 kDa, 54–58 kDa and 42–44 kDa were generally recognized by sera from naturally infected pigs as well as from hyperimmunized pigs when using the five antigen extracts. The ELISA and WB techniques may be used for immunodiagnosis, using somatic adult worm antigens, to declare young pigs to be Ascaris-free but cannot be used for individual Ascaris-diagnosis in adult Iberian pigs.


1960 ◽  
Vol 37 (4) ◽  
pp. 775-782
Author(s):  
A. E. NEEDHAM

1. The difference in arginase activity between the tissues of Eisenia and those of Lumbricus shows a relationship to the difference in urea output by living worms of the two species under the same dietary régime. 2. In Eisenia the difference in activity between the tissues of fasting and feeding worms is much smaller than in Lumbricus. The specific outputs of urea by living, fasting and feeding worms likewise differ less than in Lumbricus. 3. These facts strengthen previous evidence in favour of a Krebs-Henseleit type of mechanism for urea production in earthworms. 4. In Eisenia the difference in arginase activity between gut and body wall is similar to, but smaller than, that in Lumbricus, and the body wall makes a major contribution to the total activity. 5. The combined concentrations of ammonia-, amino-, and urea-nitrogen initially present in homogenates of the tissues of these worms are proportional to the combined amounts of the three components excreted per unit weight by living worms of the same species and régime. 6. The two species differ in a number of other properties investigated.


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