scholarly journals The Lateral Line System of Sense Organs in Some American Amphibia, and Comparison with the Dipnoans

1896 ◽  
Vol 17 ◽  
pp. 115 ◽  
Author(s):  
B. F. Kingsbury

The recognition of the morphological and developmental relationship of the vertebrate auditory organ and the lateral-line system of fishes and aquatic Amphibia rests on the foundation of a large volume of com­ parative researches. The main outlines of this generalization were already laid down forty years ago, and Cole’s work on the cranial nerves and lateral sense organs of fishes (1898) contains a comprehensive treatment of the history of the subject. The acustico-lateral or neuromast system embraces, in addition to the labyrinth and the lateral-line canals, the pit organs found to a greater or less extent in most fishes, the vesicles of Torpedo , and the ampullary canal system of Selachians and Holocephali. Concerning these Cole wrote: “The history of our knowledge of the phylogeny of the sensory canals is coincident with three discoveries—the discovery that the‘mucus’ canals contain sense organs, the discovery of Savi’s vesicles, and the dis­covery of the ampullae of Lorenzini.... We now know that all three types belong to the lateral line system, and I shall suggest that they represent three stages in the development of a canal—the most superficial condition, represented by the pit organs and Savi’s vesicles; the full development, represented by the canal; and the intermediate type, forming neither a Savi vesicle nor yet a canal, represented by the ampullae of Lorenzini” (p. 187). This conception has remained valid to the present day. The ampullae of Lorenzini, with which I am here principally concerned, are briefly described in current text-books as transitional or specialized neuromasts, and the implication always is that structurally and functionally they do not differ significantly from the neuromasts of the lateral-line canals. For example, in their recent exhaustive treatise on the vertebrate nervous system Kappers, Huber and Crosby (1936) state with reference to the lateral-line canals, the Savi vesicles and the ampullae of Lorenzini: “thus in the various animals there is a transition between an open and a closed system for perceiving vibrations" (p. 438).


For a long time after their discovery in the seventeenth century the lateral-line canals of fishes were considered to be mucus-secreting organs. In 1850 Leydig described sense organs in the lateral-line canals, and this discovery stimulated a keen interest in the investigation of both the morphological and functional features of the lateral-line system. Morphological studies have yielded a thorough understanding of the structure of these organs (Ewart and Mitchell 1892; Cole 1896; Johnson 1917; von Woellwarth 1933). Physiological studies, though numerous, have been less fruitful. An account of the older work was given by Baglioni (1913), and the more recent work is reviewed by Dykgraaf (1933). The only technique until recently available has been the elimination of the sensory system by nerve section and cauterization, and the comparison of the behaviour of intact and operated fishes in response to various stimuli. With so diffuse a structure as the lateral-line system, receiving its nerve supply from the fifth, seventh, ninth and tenth cranial nerves, this method is particularly inadequate, and involves a violent mutilation of the animal. When one considers the crudity of many of these operations, it is not the uncertainty of the results which is remarkable, but rather that some of the conclusions reached should remain valid to-day in the light of far more penetrating experimental analysis. This method of organ elimination could yield at best only an indication of the kind of stimulus that is effective in evoking the excitation of lateral-line receptors. In current textbooks the conclusion of Parker (1904) that the effective stimulus for the lateral line is low-frequency vibration, and that of Hofer (1907) that it is movement of water (i. e. local currents) have received most notice. The observations of Dykgraaf (1933), who employed the more refined methods of von Frisch’s futterdressur technique, support Hofer’s conclusion, and to some extent also Parker’s. Dykgraaf considers the lateral-line system to be an organ of Ferntastsinn , and if this is taken to mean a mechanoreceptor of such sensitivity that it can function both as a touch organ and as a receptor for disturbances coming from a distance, it is undoubtedly a true description, for it is fully confirmed by the direct electrophysiological studies of Hoagland (1933 a, b, c and d ) and of Schriever (1935). The latter, apparently unacquainted with Hoagland’s work, did little more than to confirm several of his observations.


Author(s):  
Jennifer D. Liddicoat ◽  
B. L. Roberts

The sense organs of the lateral-line system of lower aquatic vertebrates are mechanoreceptors which respond to water movements. They are distributed over the body, usually in lines which form a definite pattern on the head and along each side of the trunk. In the Cyclostomes the sense organs project from the body surface ('free neuromasts'); in other aquatic vertebrates they are usually housed in canals which are sunk into the dermis and which open at regular intervals to the exterior, although in some teleosts and in all modern amphibia the canal system has been secondarily lost and the neuromasts are once again situated externally.


Author(s):  
T. S. Kemp

‘The amphibians’ world’ focuses on the amphibians’ sense organs. Amphibians have the eyes, ears, olfactory organs of smell in the nose, and touch receptors common to all vertebrates, but the relative importance of the different senses varies from group to group depending on habitats and modes of life. Anurans have a sensory world most like that of humans; their vision is good, and includes the ability to see colours, and their hearing is acute. Urodeles and caecilians rely much more on their senses of smell and touch. Amphibian larvae have an additional sensory system called the lateral line system. Amphibians use several sensory cues in combination to navigate around their territories.


1933 ◽  
Vol 16 (4) ◽  
pp. 715-732 ◽  
Author(s):  
Hudson Hoagland

1. The lateral-line nerves of trout as well as those of catfish are found to discharge impulses spontaneously at a high frequency. 2. The frequency of nerve impulse discharge is measured as a function of the number of participating receptor groups (lateral-line sense organs). A quantitative analysis is made of the contribution to the total response made by each group of sense organs. 3. An analysis of the variability of the response is presented which makes it possible to estimate quantitatively the longitudinal extent of damage to the neuromasts due to surgical manipulation. 4. A method is described for recording the response of a single nerve fiber in the lateral-line trunk. 5. The frequency of the spontaneous discharge from the lateral-line nerve trunk when plotted as a function of temperature according to the Arrhenius equation yields a temperature characteristic of approximately 5000 calories. 6. The variability of the frequency of response as a function of temperature indicates the existence of temperature thresholds for the spontaneous activity of the neuromasts. 7. A possible basis for the spontaneous activity is considered. It is pointed out that the lateral-line system may serve as a model of the Purkinje cells of the cerebellum.


1895 ◽  
Vol 20 ◽  
pp. 475-480 ◽  
Author(s):  
J. C. Ewart ◽  
F. J. Cole

The Glossopharyngeal.—The glossopharyngeal is usually looked upon as the most typical of the cranial nerves. In Amia, according to Allis, it consists of post- and præ-branchial branches, a visceral or pharyngeal branch, and a dorsal branch which takes part in innervating the lateral line system—supplying by a single twig one of the sense organs of the lateral canal, and in addition a row of pit organs.


1951 ◽  
Vol 26 (3) ◽  
pp. 264-280 ◽  
Author(s):  
Margaret R. Wright

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