1959
DOI: 10.1002/jez.1401410202
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The physiology of the spider vibration receptor

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Cited by 74 publications
(18 citation statements)
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“…This may allow them to detect and discriminate potential nearby prey and predators (22,23), which is different from the well-known substrate-borne information transmission induced by animals making direct contact with the silk (24)(25)(26)(27).…”
Section: Significancementioning
confidence: 87%
“…This may allow them to detect and discriminate potential nearby prey and predators (22,23), which is different from the well-known substrate-borne information transmission induced by animals making direct contact with the silk (24)(25)(26)(27).…”
Section: Significancementioning
confidence: 87%
“…A single slit in this position is reported for the ctenid Czipiennius s a k i (Barth & Libera, 1970), while Foelix (1970b: figs 16, 17) apparently figures a series of slit sensilla in this position for Aruneus diadernatus (Araneidae), without noting their presence. Barth (1971) provides an excellent description of the morphology of slit sensilla, while others (Pringle, 1955;Walcott & van der Kloot, 1959) have provided good evidence for the function of arachnid slit sensilla as mechanoreceptors. The slit sensilla of the spider are thought to provide information in regard to cuticular stress, particularly when that stress is perpendicular to the sensillum and the deformation of the cuticle (strain) is maximized (Barth, 1972;Seyfarth & Barth, 1972).…”
Section: Slit Sensillamentioning
confidence: 99%
“…Again, it is not clear that extrapolation to small displacements is always justified (see Walcott and van der Kloot 1959), but since similar tuning curves and thresholds were obtained by both Autrum and Schneider ( 1948) and Schnorbus ( 197 1 a,b) using different devices, this potential pitfall may not have been important in practice.…”
Section: Critique Of Previous Attempts To Measure Absolute Vibration mentioning
confidence: 82%
“…As part of a comparative study, Autrum and Schneider ( 1948) attached isolated mesothoracic legs to the vibrating coil of a dynamic speaker from which the main diaphragm had been removed, so that the whole leg was vibrated as a unit. Again, it is not clear that extrapolation to small displacements is always justified (see Walcott and van der Kloot 1959), but since similar tuning curves and thresholds were obtained by both Autrum and Schneider ( 1948) and Schnorbus ( 197 1 a,b) using different devices, this potential pitfall may not have been important in practice. Potentially a more serious problem with the experimental designs of both Autrum and Schneider ( 1948) and Schnorbus (1971a,b) is that their vibrators accelerated the entire leg through stationary air, necessarily generating pressure transients in the cut ends of the large tracheae at the surface of amputation.…”
Section: Absolute Vibration Threshold In Cockroach Legsmentioning
confidence: 96%