The Mechanosensory Lateral Line System of the Hypogean form of Astyanax Fasciatus

The mechanosensory lateral line is a distributed, hair-cell based system which detects the water flow regime at the surface of the fish. Superficial neuromasts densely scattered over the surface of some cave fish detect the pattern of flow over the surface of the body and are important in rheotactic behaviors and perhaps in the localization of small vibrating sources. Canal neuromasts are very likely also involved in the detection of small planktonic prey, but seem also to play an essential role in replacing vision as the major sense by which blind cave-fish perceive their surroundings. The flow-field that exists around a gliding fish is perturbed by objects in the immediate vicinity, these perturbations are detected by the lateral line system. In this way the fish can build up a ‘picture’ of its environment, a process that has been called active hydrodynamic imaging. None of the lateral line behaviors exhibited by blind cave fish are necessarily exclusive to these species, but there is some evidence that their lateral line capabilities are enhanced with respect to their sighted relatives.

[1]  T. Poulson Cave Adaptation in Amblyopsid Fishes , 1963 .

[2]  S. Dijkgraaf THE FUNCTIONING and SIGNIFICANCE OF THE LATERAL‐LINE ORGANS , 1963, Biological reviews of the Cambridge Philosophical Society.

[3]  Lateral-line sensitivity in the blind cavefish (Anoptichthys jordani). , 1970 .

[4]  Kathy M. Shumaker,et al.  PATTERNS OF ALLOZYMIC SIMILARITY IN ECOLOGICALLY CENTRAL AND MARGINAL POPULATIONS OF HORDEUM JUBATUM IN UTAH , 1980, Evolution; international journal of organic evolution.

[5]  J. Janssen,et al.  Lateral Line Receptivity in the Mottled Sculpin (Cottus bairdi) , 1986 .

[6]  J. Parzefall Behavioural Ecology of Cave-Dwelling Fishes , 1986 .

[7]  T. Pitcher Behaviour of Teleost Fishes , 1986 .

[8]  J. Montgomery,et al.  Sensory Tuning of Lateral Line Receptors in Antarctic Fish to the Movements of Planktonic Prey , 1987, Science.

[9]  Jelle Atema,et al.  Sensory Biology of Aquatic Animals , 1988, Springer New York.

[10]  S. Coombs,et al.  Diversity of Lateral Line Systems: Evolutionary and Functional Considerations , 1988 .

[11]  J. Gray,et al.  Mechanical Factors in the Excitation of the Lateral Lines of Fishes , 1988 .

[12]  E. Hassan Hydrodynamic Imaging of the Surroundings by the Lateral Line of the Blind Cave Fish Anoptichthys jordani , 1989 .

[13]  J. Montgomery Lateral Line Detection of Planktonic Prey , 1989 .

[14]  R L Puzdrowski,et al.  Peripheral distribution and central projections of the lateral-line nerves in goldfish, Carassius auratus. , 1989, Brain, behavior and evolution.

[15]  T Teyke,et al.  Morphological differences in neuromasts of the blind cave fish Astyanax hubbsi and the sighted river fish Astyanax mexicanus. , 1990, Brain, behavior and evolution.

[16]  S Coombs,et al.  Form and function relationships in lateral line systems: comparative data from six species of Antarctic notothenioid fish. , 1994, Brain, behavior and evolution.

[17]  Jiakun Song,et al.  Damage and recovery of hair cells in fish canal (but not superficial) neuromasts after gentamicin exposure , 1995, Hearing Research.

[18]  J. Montgomery,et al.  The lateral line can mediate rheotaxis in fish , 1997, Nature.

[19]  John C. Montgomery,et al.  The Enigmatic Lateral Line System , 1999 .

[20]  Olfactory search tracks in the Antarctic fish Trematomus bernacchii , 1999, Polar Biology.

[21]  C. F. Baker,et al.  The sensory basis of rheotaxis in the blind Mexican cave fish, Astyanax fasciatus , 1999, Journal of Comparative Physiology A.

[22]  S. Coombs,et al.  The orienting response of Lake Michigan mottled sculpin is mediated by canal neuromasts. , 2001, The Journal of experimental biology.

[23]  A. Romero Behavior in an ‘intermediate’ population of the subterranean-dwelling characid Astyanax fasciatus , 1984, Environmental Biology of Fishes.

[24]  T. Teyke,et al.  Flow field, swimming velocity and boundary layer: parameters which affect the stimulus for the lateral line organ in blind fish , 1988, Journal of Comparative Physiology A.

[25]  El-S. Hassan Mathematical description of the stimuli to the lateral line system of fish derived from a three-dimensional flow field analysis , 2004, Biological Cybernetics.

[26]  J. Janssen,et al.  Non-visual feeding behavior of the mottled sculpin, Cottus bairdi, in Lake Michigan , 1985, Environmental Biology of Fishes.

[27]  E. Hassan,et al.  Studies on the effects of Ca2++ and Co++ on the swimming behavior of the blind Mexican cave fish , 1992, Journal of Comparative Physiology A.

[28]  El-S. Hassan,et al.  Mathematical description of the stimuli to the lateral line system of fish, derived from a three-dimensional flow field analysis. III. The case of an oscillating sphere near the fish , 1993, Biological Cybernetics.

[29]  T. Teyke,et al.  Learning and remembering the environment in the blind cave fishAnoptichthys jordani , 1989, Journal of Comparative Physiology A.

[30]  El-S. Hassan,et al.  Mathematical description of the stimuli to the lateral line system of fish derived from a three-dimensional flow field analysis , 1992, Biological Cybernetics.

[31]  C. Schemmel Vergleichende Untersuchungen an den Hautsinnesorganen ober- und unterirdisch lebender Astyanax-Formen , 1967, Zeitschrift für Morphologie der Tiere.

[32]  E. Hassan,et al.  On the discrimination of spatial intervals by the blind cave fish (Anoptichthys jordani) , 1986, Journal of Comparative Physiology A.

[33]  C. Campenhausen,et al.  Detection of stationary objects by the blind Cave FishAnoptichthys jordani (Characidae) , 1981, Journal of comparative physiology.

[34]  T. Teyke,et al.  Collision with and avoidance of obstacles by blind cave fishAnoptichthys jordani (Characidae) , 1985, Journal of Comparative Physiology A.

[35]  C. Campenhausen,et al.  Sensory performance of blind mexican cave fish after destruction of the canal neuromasts , 1990, Naturwissenschaften.