Sensory ecology of ostariophysan alarm substances

Author(s):  
Caio Maximino ◽  
Rhayra X. do Carmo Silva ◽  
Kimberly dos Santos Campos ◽  
Jeisiane S. de Oliveira ◽  
Sueslene P. Rocha ◽  
...  
Author(s):  
Caio Maximino ◽  
Rhayra Xavier do Carmo Silva ◽  
Kimberly dos Santos Campos ◽  
Jeiseane Souza de Oliveira ◽  
Sueslene Prado Rocha ◽  
...  

Chemical communication of predation risk has evolved multiple times in fish species, with the conspecific alarm substance (CAS) contemporaneously being the most well understood mechanism. CAS is released after epithelial damage, usually when prey fish is captured by a predator, and elicits neurobehavioral adjustments in conspecifics which increase the probability of avoiding predation. As such, CAS is a partial predator stimulus, eliciting risk assessment-like and avoidance behaviors, and disrupting the predator sequence. The present paper reviews the distribution and putative composition of CAS in fish, and presents a model for the neural processing of these structures by the olfactory and the brain aversive systems. Applications of CAS in the behavioral neurosciences and neuropharmacology are also presented, exploiting the potential of model fish (e.g., zebrafish, guppies, minnows) on neurobehavioral research.


Author(s):  
Caio Maximino ◽  
Rhayra Xavier do Carmo Silva ◽  
Kimberly dos Santos Campos ◽  
Jeiseane Souza de Oliveira ◽  
Sueslene Prado Rocha ◽  
...  

Chemical communication of predation risk has evolved multiple times in fish species, with the conspecific alarm substance (CAS) contemporaneously being the most well understood mechanism. CAS is released after epithelial damage, usually when prey fish is captured by a predator, and elicits neurobehavioral adjustments in conspecifics which increase the probability of avoiding predation. As such, CAS is a partial predator stimulus, eliciting risk assessment-like and avoidance behaviors, and disrupting the predator sequence. The present paper reviews the distribution and putative composition of CAS in fish, and presents a model for the neural processing of these structures by the olfactory and the brain aversive systems. Applications of CAS in the behavioral neurosciences and neuropharmacology are also presented, exploiting the potential of model fish (e.g., zebrafish, guppies, minnows) on neurobehavioral research.


2008 ◽  
Vol 49 (1) ◽  
pp. 4
Author(s):  
Carper
Keyword(s):  

The Auk ◽  
2021 ◽  
Author(s):  
Kristina Fialko ◽  
Jarome R Ali ◽  
Laura Céspedes Arias ◽  
Jacob Drucker ◽  
Klara K Nordén ◽  
...  
Keyword(s):  

1995 ◽  
Vol 26 (2-4) ◽  
pp. 101-118 ◽  
Author(s):  
William M. Hamner
Keyword(s):  

2014 ◽  
pp. 3-17
Author(s):  
Martín M. Kowalewski ◽  
Paul A. Garber ◽  
Liliana Cortés-Ortiz ◽  
Bernardo Urbani ◽  
Dionisios Youlatos

2010 ◽  
Vol 6 (4) ◽  
pp. 525-528 ◽  
Author(s):  
S. Mourabit ◽  
S. D. Rundle ◽  
J. I. Spicer ◽  
K. A. Sloman

Alarm substances elicit behavioural responses in a wide range of animals but effects on early embryonic development are virtually unknown. Here we investigated whether skin injury-induced alarm substances caused physiological responses in embryos produced by two Danio species ( Danio rerio and Danio albolineatus ). Both species showed more rapid physiological development in the presence of alarm substance, although there were subtle differences between them: D. rerio had advanced muscle contraction and heart function, whereas D. albolineatus had advanced heart function only. Hence, alarm cues from injured or dying fish may be of benefit to their offspring, inducing physiological responses and potentially increasing their inclusive fitness.


2021 ◽  
Vol 288 (1953) ◽  
pp. 20210774
Author(s):  
Beth Mortimer ◽  
James A. Walker ◽  
David S. Lolchuragi ◽  
Michael Reinwald ◽  
David Daballen

African elephants ( Loxodonta africana ) use many sensory modes to gather information about their environment, including the detection of seismic, or ground-based, vibrations. Seismic information is known to include elephant-generated signals, but also potentially encompasses biotic cues that are commonly referred to as ‘noise’. To investigate seismic information transfer in elephants beyond communication, here we tested the hypothesis that wild elephants detect and discriminate between seismic vibrations that differ in their noise types, whether elephant- or human-generated. We played three types of seismic vibrations to elephants: seismic recordings of elephants (elephant-generated), white noise (human-generated) and a combined track (elephant- and human-generated). We found evidence of both detection of seismic noise and discrimination between the two treatments containing human-generated noise. In particular, we found evidence of retreat behaviour, where seismic tracks with human-generated noise caused elephants to move further away from the trial location. We conclude that seismic noise are cues that contain biologically relevant information for elephants that they can associate with risk. This expands our understanding of how elephants use seismic information, with implications for elephant sensory ecology and conservation management.


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