scholarly journals First record of Gymnotus henni (Albert, Crampton and Maldonado, 2003) in Panama: phylogenetic position and electric signal characterization

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2013 ◽  
Vol 9 (3) ◽  
pp. 655 ◽  
Author(s):  
Fernando Alda ◽  
Sophie Picq ◽  
Luis Fernando De León ◽  
Rigoberto González ◽  
Henriette Walz ◽  
...  

We present the first record of the weakly electric fish Gymnotus henni in Panama, which also represents the first record of Gymnotus in the Pacific slope of the country. One specimen was collected in a tributary of the Chucunaque River in the Tuira basin. The species showed a monophasic electric organ discharge. Molecular analyses indicated that G. henni from Panama and Colombia are closely related and represent an independent and basal lineage to the Central American G. cylindricus and South American G. carapo groups. Evolutionary and biogeographic implications are discussed.

2000 ◽  
Vol 203 (3) ◽  
pp. 481-492 ◽  
Author(s):  
R. Budelli ◽  
A.A. Caputi

Weakly electric fish explore the environment using electrolocation. They produce an electric field that is detected by cutaneous electroreceptors; external objects distort the field, thus generating an electric image. The electric image of objects of complex impedance was investigated using a realistic model, which was able to reproduce previous experimental data. The transcutaneous voltage in the presence of an elementary object is modulated in amplitude and waveform on the skin. Amplitude modulation (measured as the relative change in the local peak-to-peak amplitude) consists of a ‘Mexican hat’ profile whose maximum relative slope depends on the distance of the fish from the object. Waveform modulation depends on both the distance and the electrical characteristics of the object. Changes in waveform are indicated by the amplitude ratio of the larger positive and negative phases of the local electric organ discharge on the skin. Using the peak-to-peak amplitude and the positive-to-negative amplitude ratio of this discharge, a perceptual space can be defined and correlated with the capacitance and resistance of the object. When the object is moved away, the perceptual space is reduced but keeps the same proportions (homothetically): for a given object, the positive-to-negative amplitude ratio is a linear function of the peak-to-peak amplitude. This linear function depends on the electrical characteristics of the object. However, there are ‘families’ of objects with different electrical characteristics that produce changes in the parameters of the local electric organ discharge that are related by the same linear function. We propose that these functions code the perceptual properties of an object related to its impedance.


1993 ◽  
Vol 71 (11) ◽  
pp. 2301-2310 ◽  
Author(s):  
Günther K. H. Zupanc ◽  
Leonard Maler

Apteronotus leptorhynchus, a gymnotiform fish, produces highly regular electric organ discharges of 600–1000 Hz. Short-term modulations of the electric organ discharge ("chirps") were elicited by imitating the discharges of neighboring fish. Chirps displayed an increase in frequency of approximately 100 Hz, a duration of about 15 ms, and an absolute amplitude of 0.5–2 mV. Since, similar to natural conditions, chirps summated with the beat caused by interference of the fish's own electric organ discharge and the imitating discharge, the size and shape of the chirp's amplitude envelope varied greatly according to its phase relative to the beat cycle; however, the frequency of the chirp amplitude modulation was always 50–100 Hz. All 21 males examined chirped, but their rate of chirping varied considerably (range 2–59 chirps/30 s; mean 22 chirps/30 s). In contrast, only one out of nine females chirped (mean 0.25 chirps/30 s). The latency between stimulus onset and first chirp was variable and often long (range 1.0–25.0 s; median 3.3 s). We propose that chirps are not a sensory reflex but a communicatory behavior regulated by hypothalamic peptidergic input.


2010 ◽  
Vol 7 (2) ◽  
pp. 197-200 ◽  
Author(s):  
Vincent Fugère ◽  
Hernán Ortega ◽  
Rüdiger Krahe

Animals often use signals to communicate their dominance status and avoid the costs of combat. We investigated whether the frequency of the electric organ discharge (EOD) of the weakly electric fish, Sternarchorhynchus sp., signals the dominance status of individuals. We correlated EOD frequency with body size and found a strong positive relationship. We then performed a competition experiment in which we found that higher frequency individuals were dominant over lower frequency ones. Finally, we conducted an electrical playback experiment and found that subjects more readily approached and attacked the stimulus electrodes when they played low-frequency signals than high-frequency ones. We propose that EOD frequency communicates dominance status in this gymnotiform species.


2000 ◽  
Vol 203 (9) ◽  
pp. 1433-1446 ◽  
Author(s):  
S. Schuster

During their entire lives, weakly electric fish produce an uninterrupted train of discharges to electrolocate objects and to communicate. In an attempt to learn about activity-dependent processes that might be involved in this ability, the continuous train of discharges of intact Gymnotus carapo was experimentally interrupted to investigate how this pausing affects post-pause electric organ discharges. In particular, an analysis was conducted of how the amplitude and relative timing of the three major deflections of the complex discharge change over the course of the first 1000 post-pause discharges. The dependence of these variables on the duration of the preceding pause and on water temperature is analysed. In addition, pause-induced small reverberations at the end of the discharge are described. Common to all amplitude changes is a fast initial decrease in amplitude with a slow recovery phase; amplitude changes scale with the duration of the preceding pause and are independent of the interdischarge interval. The absence of changes in the postsynaptic-potential-derived first phase of the discharge together with changes in the amplitude ratio of the third and fourth deflections suggest that the amplitude changes are mainly due to pause-induced changes in the inner resistance of the electric organ. A model is formulated that approximates the pattern of amplitude changes. The post-pause changes described here may provide a new way to test current models of complex discharge generation in Gymnotus carapo and illustrate the speed at which changes of an electric organ discharge can take place.


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