A Note on the Habits and Nutrition of Solemya parkinsoni (Protobranchia: Bivalvia)

1961 ◽  
Vol s3-102 (57) ◽  
pp. 15-21
Author(s):  
G. OWEN

Adult specimens of Solemya parkinsoni Smith, embedded in mud at a depth of 50 cm or more, were collected near low water (spring tide). The animal burrows with the anterior end downwards and does not maintain an opening to the surface. An inhalant current is drawn into the mantle cavity anteriorly on each side of the foot, while an exhalant current leaves by the single, posteriorly situated aperture. This is probably a respiratory current, bottom material entering the mantle cavity as a result of the muscular activity of the mantle and foot. The course of the alimentary canal is described, and the problem of feeding and nutrition correlated with the extreme reduction of the gut exhibited by S.parkinsoni discussed. It is suggested that an initial breakdown of organic material may take place in the mantle cavity.

1942 ◽  
Vol s2-83 (331) ◽  
pp. 357-397 ◽  
Author(s):  
H. H. HOWELLS

1. The anatomy and histology of the alimentary canal, process of feeding, and physiology of digestion in Aplysia punctata have been investigated. 2. The food undergoes little trituration in the buccal cavity. The mode of action of the jaws and odontophore is adapted to the rapid intake of vegetable food. 3. The oesophagus and crop together form an anatomical and physiological unit. 4. Trituration occurs in the gizzard. The teeth are adapted to the trituration of plant material; this is of particular importance owing to the weak action of the cellulase. 5. Coarser particles of weed are retained by the teeth of the filter chamber and returned to the gizzard during the forward movement of the gut fluid. 6. The ciliary currents in the anterior intestine ensure that only food in a finely divided or fluid state is admitted to the stomach. Medium and larger sized particles are carried straight into the intestine. 7. Ciliary currents in the stomach are concerned with the removal of material rejected from the tubules of the digestive diverticula. This material is consolidated, cemented, and moulded into a faecal rod within the caecum, and conveyed by ciliary action to the intestine. 8. The intestine is concerned with the further consolidation and moulding of the complete faecal mass, and its propulsion (by combined ciliary and muscular action) to the rectum. 9. Mucus is secreted throughout the gut with the exception of the regions of the jaws, gizzard, and filter chamber. Enzymes are secreted in the salivary glands (amylase and protease) and in the digestive diverticula (carbohydrases, lipase, and proteases). Glands probably secreting a lubricant (other than mucus) occur in the epithelium of the lateral walls of the buccal cavity, and others, secreting a cementing substance, in the caecum and intestine. 10. Absorptive cells occupy the greater part of the epithelium of the digestive diverticula. They occur together with secretory, excretory, and storage cells. 11. Digestion occurs within the oesophagus and crop, gizzard, filter chamber, anterior intestine, stomach, and tubules of the digestive diverticula. The hydrogen ion concentration is here suitable for the action of the enzymes, and the gut fluid is kept in motion by the muscular activity of the walls. 12. A high pH exists in the lumen of the caecum, posterior intestine, and rectum, probably assisting in the consolidation of the faecal mass by increasing the viscosity of the mucus. 13. The presence of a highly efficient mechanism for the formation of the faeces is probably correlated with the poorly developed cleansing mechanism in the mantle cavity.


1928 ◽  
Vol s2-71 (284) ◽  
pp. 563-651
Author(s):  
GUY D. MORISON

1. The entire musculature of the alimentary canal is described in gross and in histological detail. The development of the muscle is considered. The innervation is described, likewise the tracheation and its relation to muscular activity and the bloodstream. 2. The heart is described with a detailed histological account of its muscle-fibres. Its tracheation is described and its apparent lack of innervation is discussed. 3. The ‘alary’ muscles of the dorsal diaphragm are described with a detailed account of their histology, innervation, and tracheation. 4. The ventral diaphragm is described as well as the histology, innervation, and tracheation of its muscle-fibres. The course of blood and physiological questions connected with it receive discussion. 5. The muscles of the reproductive organs of drone, queen, and worker are described with particular reference to the histology, innervation, tracheation, and physiology of their fibres. 6. The indirect muscles of the wings (fibrous muscle) have their histology, innervation, and tracheation described in detail. The method of contraction of the entire muscles and of the individual fibres and fibrils is discussed. The sarcosomes are described with their physiological significance to contraction. 7. The attachment of all the types of muscle found in the bee is described in histological detail. Different opinions of muscle attachment to chitin are summarized. 8. Throughout the paper, histological measurements are given for the various types of muscle-fibres and their nuclei in the three castes of bee. Since in the three castes the histological appearance is so similar for each type of muscle, the illustrations have been limited to portions of the muscles of worker bees.


Author(s):  
C. M. Yonge

The anatomy and histology of the food collecting and alimentary organs of the adult oyster are described.The anatomy of the stomach is investigated with the aid of gelatin casts and attention drawn to the food caecum, the ventral groove, and the two ducts of the digestive diverticula.Cilia and mucus glands are universal throughout the food collecting and alimentary organs.There is evidence that the gastric shield is composed of fused cilia.The histology of the style-sac resembles that described by Mackintosh for Crepidula. There is evidence that secretion of the style takes place in the groove.Phagocytes are everywhere numerous in the blood vessels, connective tissue and epithelia, and free in the gut and mantle cavity.The alimentary organs of the larva are described.The anatomy and histology of these organs in the spat isdescribed, the palps are relatively large and the gills asymmetrical. The style-sac is distinct from the mid-gut.The course of the ciliary currents on the gills and palps is described and the importance of the various selective mechanisms emphasized.Selection appears to be purely quantitative, large particles or mucus masses being rejected and smaller ones accepted.Muscular activity is of great importance in the functioning of both gills and palps. Reversal of cilia has never been seen.Rejected matter is removed from the mantle cavity.Material is sorted in the food caecum in the stomach, larger particles passing into the mid-gut and smaller ones towards the gastric shield and ducts of the digestive diverticula, within the tubules of which there is a constant circulation.The rotation of the style assists in the stirring of matter in the stomach.In the style-sac are cilia, which rotate the style and others which push it into the storuach.In the larva the velum acts as a food collecting organ ; the style lies in an extension of the stomach and rotates rapidly. Material passes freely into the digestive diverticula.In the spat rejective mechanisms are highly developed. The style revolves at a speed of between sixty and seventy revolutions per minute.The tubules of the digestive diverticula are the only place where soluble matter is absorbed, in adult, larvae, or spat.Fine particles are ingested and digested intracellularly in the tubules of the digestive diverticula, the products of digestion carried away by amoebocytes, and useless matter rejected into the lumen.Larger particles are ingested and digested by phagocytes in all parts, the products of digestion being carried to the vesicular connective tissue cells and there stored.Enzymes in the style digest starch and glycogen. The amylase, at pH 5.9, has an optimum temperature of 43'C, and is destroyed atThe optimum medium is pH 5-9. It is inactivated by purification with absolute alcohol or by dialysis, but action is restored on the addition of chlorides or bromides and to a less extent iodides, nitrates, and carbonates, but not with sulphates or fluorides.Sucroclastic enzymes in the digestive diverticula act on starch, glycogen, sucrose, raffinose, maltose, lactose, salicin, and amygdalin, but not on inulin, cellulose, or pentosans.The amylase, at pH 5-5, has an optimum temperature of 44-5, and is destroyed at between 64 and 67. It has an optimum pH of 5-5, and is inactivated after purification or dialysis, action being restored in the presence of chlorides or bromides.There is a weak lipase and protease, the latter has two optima at pH 3-7 and at or above 9-0 ; its action is very slow.The only enzymes free in the stomach are those from the style.There is no evidence of any enzymes free in the gill mucus.There is a powerful complete oxidase system in the style, and a catalase in the digestive diverticula and gonad, and traces in the palps, gills, and muscle.The style is the most acid substance in the gut and the cause of the acidity of the gut.The style is dissolved rapidly in fluid of pH 2-3 and above, but very slowly below that point. It is readily dissolved and reformed in the oyster, its presence depending on the maintenance of the balance between the rate of secretion and the rate of dissolution. Its condition is a valuable indication of the state of metabolism.Glycogen and fat are stored, particularly in the vesicular connective tissue cells, the former furnishing the principal reserve food material.The presence of abundant supplies of microscopic plant life rich in carbohydrates provides ideal food for the oyster, and represents optimum conditions for fattening and reproduction.


Author(s):  
C. M. Yonge

SUMMARYNormal healthy oysters with openings drilled in both inhalent and exhalent chambers, remove considerable amounts of glucose from solution. The average diminution in 5 experiments, each consisting of two such animals kept in 4 litres of sea-water containing about 0-2% of glucose, was 8-17% at the end of 36 hours.In similar experiments, using the same oysters after their mouths had been plugged with wax and plasticine, there was only an average diminution of 1-4:6% in the glucose at the end of 36 hours. In two of the experiments there was no diminution, and in the three others there was evidence that one of the two oysters in each had been incompletely plugged and glucose had passed into the alimentary canal.Oysters which had been plugged for 8 days so that they were bleeding profusely, the mantle cavity containing vast numbers of leucocytes, were used for a third set of experiments in which the average diminution was 7-4% at the end of 36 hours.There was no evidence of bacterial decomposition of glucose within the experimental period.These results, taken with those of previous investigations, show that the ciliated epithelia of Lamellibranchs cannot absorb (nor ingest phagocytically). Absorption takes place in the tubules of the digestive diverticula within the alimentary canal, and, in the mantle cavity, only through the agency of phagocytes which are extruded in great numbers when Lamellibranchs bleed as a result of bad conditions.The opinion of Ranson that Marennin and other soluble matter is absorbed directly by the ciliated epithelia in the mantle cavity cannot be upheld, this material being deposited in the cells by the phagocytes which either absorb it directly from the mantle cavity and gut, or transport it from the digestive diverticula.


1976 ◽  
Vol 54 (4) ◽  
pp. 482-500 ◽  
Author(s):  
Brian Morton

The Southeast Asian mangrove is inhabited by a number of bivalves one of which, Polymesoda (Geloina) erosa (Solander, 1786), is widely distributed; it occurs on the landward fringe, in fetid pools of water formed at the bases of the mangrove trees. It is covered only by spring tides and at other times is inundated by rainwater draining through the mangrove from the land. G. erosa can withstand long periods of exposure, during which time it can use subterranean water contained in the burrow. Any particles present in this water are taken into the mantle cavity via the pedal gape and so into the alimentary canal. This is an extreme adaptation to a semiterrestrial mode of life. Aerial respiration is also achieved via the mantle margin.The functional morphology of G. erosa is described and related to the animal's life in the mangrove. The morphological adaptations of Geloina are also compared with those of other bivalves, particularly the Dreissenacea to which the Corbiculacea are possibly closely related.


1974 ◽  
Vol 61 (2) ◽  
pp. 411-419
Author(s):  
A. PACKARD ◽  
E. R. TRUEMAN

1. The action of the mantle of Sepia and Loligo has been monitored under nearly natural conditions. Respiratory movements are confined to the anterior mantle whilst during jet cycles the circular muscles contract powerfully throughout the mantle. 2. Contraction of circular muscle results in thickening of the mantle and expulsion of water from the mantle cavity. Activity of radial muscles causes the mantle to become thinner and to expand in surface area so as to inhale water. 3. During such movements these two groups of muscles antagonize each other directly without the participation of a discrete skeleton.


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