Waveform generation in Rhamphichthys rostratus (L.) (Teleostei,Gymnotiformes)

Rhamphichthys rostratus (L.) emits brief pulses (2 ms) repeated very regularly at 50 Hz. The electric organ shows a heterogeneous distribution of the electrocyte tubes and the occurrence of three electrocyte types (caudally innervated, rostrally innervated and marginallycaudally innervated). In the sub-opercular region the electric organ consists of a pair of tubes containing only caudally innervated electrocytes. At the abdominal region the EO consists of three pairs of tubes. Each pair contains one of the described electrocyte types. The number of electrocyte tubes increases toward the tail to reach nine or ten pairs in the most caudal segments. In the intermediate region most tubes contain doubly innervated electrocytes except the ventral pair that contains caudally innervated electrocytes. The caudal 25% contains exclusively caudally innervated electrocytes. The electric organ discharge consists of five wave components (V1 to V5). Electrophysiological data are consistent with the hypothesis that V1 results from the activity of the rostral faces of rostrally innervated electrocytes. V2 results from the activities of rostral faces of marginally-caudally innervated electrocytes while V3 results from the activities of caudal faces of most electrocytes. Curarization experiments demonstrated that V4 and V5 result from action potential invasion and are not directly elicited by neural activity.Abbreviations AEN1 anterior electromotor nerve 1 - AEN2 anterior electromotor nerve 2 - BMB boraxic methylene blue - CIE caudally innervated electrocytes - EMF electromotive force - EO electric organ - EOD electric organ discharge - I current amplitude - MCIE marginally-caudally innervated electrocytes - MT medial tubes - PEN posterior electromotor nerve - R _n internal impedance - RIE rostrally innervated electrocytes - Rl load resistor - SAT short abdominal tubes - V voltage amplitude     

Spatial distribution of the medullary command signal within the electric organ of Gymnotus carapo

The pacemaker nucleus of Gymnotus carapo contains two types of neurons: pacemaker cells which set up the frequency of the electric organ discharge (EOD) and relay cells which convey the command signal to the spinal cord. Direct activation of a single relay cell provides enough excitation to discharge a pool of spinal electromotor neurons and electrocytes, generating a small EOD (unit EOD). Different relay cells generate unit EODs of variable size and waveform, indicating the involvement of different groups of electrocytes. A special technique of EOD recording (multiple air-gap) was combined with intracellular stimulation of relay cells to study the spatial distribution within the electric organ (EO) of the command signal arising from different relay cells. Three types of relay cells could be identified: type I commanding the rostral 10% of the EO, type II which distribute their command all along the EO and type III driving the caudal 30%. Waveform analysis of unit EODs indicates that doubly innervated electrocytes which are the most relevant for attaining the specific EOD waveform, receive a favored command from the pacemaker nucleus.Abbreviations CV conduction velocity - EMF electromotive force - EMN electromotor neuron - EO electric organ - EOD electric organ discharge - PN pacemaker nucleus - uEOD unit electric organ discharge     

A hormone-sensitive communication system in an electric fish

The electric communication system includes both special muscle-derived cells or electrocytes that produce species-typical electric signals, or electric organ discharges (EODs), and specialized sensory receptors, or electroreceptors, that encode the electric fields set up by EODs. Steroid hormones can influence the characteristic properties of both EODs and electroreceptors. Steroids appear to directly effect the anatomy and physiology of the electrocytes that generate an EOD. In contrast, the steroid effect on electroreceptors may be predominantly via an indirect mechanism whereby changes in the spectral characteristics of the EOD appear to induce changes in the spectral sensitivity of electroreceptors. Continued studies of electrosensory and electromotor systems will offer insights into the cellular bases for the development and evolution of steroid-sensitive pathways in the vertebrate nervous system.     

Electric organ activation in Gymnotus carapo: Spinal origin and peripheral mechanisms

A new technique of multiple-air-gap recording was developed to study the EO activation process in Gymnotus carapo. Using this technique, the spatiotemporal pattern of electromotive force generation was investigated in normal and spinal-lesioned animals.Our data indicate that the EOD may be considered as the result of the sequential activation of 3 defined portions of the EO: the abdominal portion (included in the rostral 25% of the fish body), the central portion (comprising the intermediate 50% of the fish body) and the tail portion (the caudal 25% of the fish body). The EOD generated at each portion is characterized by: 1) timing respect to the pacemaker nucleus discharge, 2) speed of progression within the region, 3) waveform, and 4) magnitude.Spinal sections demonstrated that EMNs serving relatively small portions of the EO are widely distributed (convergence) and that surgical exclusion of relatively small portions of the spinal cord diminishes the amplitude of the EOD along an extended portion of the EO (divergence).Abbreviations EMF electromotive force - EMN electromotor-neurons - EO electric organ - EOD electric organ discharge - PMNFP pacemaker nucleus field potential - PEN posterior electromotor nerve - PNA peripheral neural activity     

Ontogeny and evolution of electric organs in gymnotiform fish

In order to further our understanding of the evolution of electric organs in the Neotropical gymnotiform fish, we studied the ontogeny of the electric organs in eight species. In Eigenmannia virescens, Sternopygus macrurus, and Apteronotus leptorhynchus the earliest electrocytes are located between muscle fibres of the hypaxial muscle (Type A electrocytes). We present arguments that these Type A electrocytes represent the plesiomorphic condition. In S. macrurus, in addition to the electrocytes in the hypaxial muscle, additional electrocytes were found in the epaxial muscle. In A. leptorhynchus a neurogenic organ develops later during ontogeny in the medial part of the hypaxial muscle in addition to the early myogenic organ. In E. virescens the early electrocytes in hypaxial muscle will degenerate later during ontogeny, and this organ will be replaced functionally by electrocytes located in the caudal appendage and below the hypaxial muscle. In Electrophorus electricus, two Gymnotus species, Rhamphichthys sp., and Brachyhypopomus pinnicaudatus the first electrocytes were found below the hypaxial muscle (Type B electrocytes); they are assumed to be the more derived stage. In R. sp., and B. pinnicaudatus the electrocytes of Type B developed directly into the adult organ. In the two Gymnotus ssp. electrocytes were also found in the medial part of the organ in-between muscle fibres of the hypaxial muscle. In E. electricus a germinative zone was observed to separate from the ventral myotome. This zone is generating electrocytes continuously so that, as a consequence, the relative proportion of electric organ to muscle increases greatly. In 45 mm long E. electricus a separation of low voltage orientation pulses and high voltage trains of pulses (shocks) was observed. A first appearance of Hunter’s organ was found in 140 mm specimens of E. electricus. The first discharges of all species studied were head- positive, with the exception of R. sp., which produced a triphasic discharge, its main component, however, being head-positive. The arguments presented indicate that the Type A electrocytes found in E. virescens, S. macrurus, and A. leptorhynchus would represent the plesiomorphic condition. On the basis of the evidence regarding the formation, cytological appearance, and anatomical location, as well as the early electrical recordings, we would hypothesise that during the evolution of gymnotiforms wave type species evolved first, and in a second step pulse type species followed. This view, however, is corroborated by only some phylogenetic hypotheses.     

The electric image in weakly electric fish: I. A data-based model of waveform generation inGymnotus carapo

Understanding how electrosensory images are generated and perceived in actively electrolocating fish requires the study of the characteristics of fish bodies as electric sources. This paper presents a model ofGymnotus carapo based on measurements of the electromotive force generated by the electric organ and the impedance of the passive tissues. A good agreement between simulated and experimentally recorded transcutaneous currents was obtained. Passive structures participate in the transformation of the electromotive force pattern into transcutaneous current profiles. These spatial filtering properties of the fish's body were investigated using the model. The shape of the transcutaneous current profiles depends on tissue resistance and on the geometry and size of the fish. Skin impedance was mainly resistive. The effect of skin resistance on the spatial filtering properties of the fish's body was theoretically analyzed.The model results show that generators in the abdominal and central regions produce most of the currents through the head. This suggests that the electric organ discharge (EOD), generated in the abdominal and central regions is critical for active electrolocation. In addition, the well-synchronized EOD components generated all along the fish produce large potentials in the far field. These components are probably involved in long-distance electrocommunication.Preliminary results of this work were published as a symposium abstract.     

Signal variation and its morphological correlates in <Emphasis Type="Italic">Paramormyrops kingsleyae</Emphasis> provide insight into the evolution of electrogenic signal diversity in mormyrid electric fish

We describe patterns of geographic variation in electric signal waveforms among populations of the mormyrid electric fish species Paramormyrops kingsleyae. This analysis includes study of electric organs and electric organ discharge (EOD) signals from 553 specimens collected from 12 localities in Gabon, West-Central Africa from 1998 to 2009. We measured time, slope, and voltage values from nine defined EOD “landmarks” and determined peak spectral frequencies from each waveform; these data were subjected to principal components analysis. The majority of variation in EODs is explained by two factors: the first related to EOD duration, the second related to the magnitude of the weak head-negative pre-potential, P0. Both factors varied clinally across Gabon. EODs are shorter in eastern Gabon and longer in western Gabon. Peak P0 is slightly larger in northern Gabon and smaller in southern Gabon. P0 in the EOD is due to the presence of penetrating-stalked (Pa) electrocytes in the electric organ while absence is due to the presence of non-penetrating stalked electrocytes (NPp). Across Gabon, the majority of P. kingsleyae populations surveyed have only individuals with P0-present EODs and Pa electrocytes. We discovered two geographically distinct populations, isolated from others by barriers to migration, where all individuals have P0-absent EODs with NPp electrocytes. At two sites along a boundary between P0-absent and P0-present populations, P0-absent and P0-present individuals were found in sympatry; specimens collected there had electric organs of intermediate morphology. This pattern of geographic variation in EODs is considered in the context of current phylogenetic work. Multiple independent paedomorphic losses of penetrating stalked electrocytes have occurred within five Paramormyrops species and seven genera of mormyrids. We suggest that this key anatomical feature in EOD signal evolution may be under a simple mechanism of genetic control, and may be easily influenced by selection or drift throughout the evolutionary history of mormyrids.     

Waveform generation of the electric organ discharge inGymnotus carapo

Summary The electric organ (EO) ofGymnotus carapo was studied using different neurohistological techniques including conventional electron microscopy. The electric tissue extends along the fish body from the pectoral girdle to the tip of the tail, constituting a single, undivided organ. However, taking into account the number, arrangement, and innervation of the electrocytes, it is possible to divide the EO into three different portions. The more rostral portion is included within the ventral wall of the abdominal cavity. It consists of singly and doubly innervated electrocytes arranged in two rows at each side of the midline. Innervation of this zone is supplied by the first 5–7 segmental nerves and by the anterior electromotor nerves. Segmental nerves terminate on the rostral faces of doubly innervated electrocytes; axons stemming from the anterior electromotor nerves end on the caudal faces of both doubly and singly innervated electrocytes. There is an intermediate body-tail region in which the electrocytes are arranged in four dorsoventral tubes (tubes 1 to 4) on each side of the midline. In this zone, doubly innervated electrocytes (confined within tube 1) coexist together with singly innervated ones, receiving nerve terminals on their caudal faces (tubes 2, 3, and 4). The innervation characteristics appear modified at more distal portions of the tail where the doubly innervated electrocytes of tube 1 are replaced by singly innervated units. The most distal portion of the EO (approximately its terminal 30%) consists of numerous, homogeneously innervated electrocytes with nerve endings distributed exclusively on their caudal faces. Nerve supply to the intermediate and distal regions derives from the posterior electromotor nerves (PENs) which appear as well-defined anatomical entities beyond the level of metamere XXVII. At the bodytail and more distal regions the innervation pattern of the EO is particularly complex. Thin nerve trunks arise from the PENs and project ventrally toward the electrocyte tubes. Before reaching the electric tissue the electromotor axons branch frequently. Our anatomical studies indicate that the EO is heterogeneous, a feature consistent with most recent electrophysiological and biophysical experiments.Abbreviations AEN anterior electromotor nerve - EMN electromotoneurons - EO electric organ - EOD electric organ discharge - LLN lateral line nerve - PEN posterior electromotor nerve     

Single electrocytes produce a sexually dimorphic signal in South American electric fish,Hypopomus occidentalis (Gymnotiformes,Hypopomidae)

Summary Hypopomus occidentalis is a weakly electric Gymnotiform fish with a pulse-type electric organ discharge (EOD).Hypopomus used in this study were taken from one of the northernmost boundaries of this species, the Atlantic drainage of Panama where the animals breed at the beginning of the dry season (December). In normal breeding populations,Hypopomus occidentalis exhibit a sexual dimorphism in EOD and morphology. Mature males are large with a broad tail and have an EOD characterized by a low peak power frequency. Females and immature males are smaller, having a slender tail and EODs with higher peak power frequencies (Fig. 1). This study describes differences in the EOD and electric organ morphology between breeding field populations of male and femaleHypopomus. Changes in physiology, morphology and EOD shape which may accompany this seasonal change were examined in steroid injected fish, using standard histological and physiological techniques.A group of females were injected with hormones (5-dihydrotestosterone (DHT), estrogen or saline) to assess changes in their morphology and EOD. Animals treated with DHT developed characteristics which mimicked the sexually dimorphic characteristics of a male, while the other groups did not (see Fig. 5). Tissue from the tails of breeding males and females, and females treated with DHT, were sampled to measure the size of the electrocytes in the tail. The broader tail of males and DHT-females is composed of large electrocytes, whereas the slender tail of normal females is composed of smaller electrocytes. Therefore, the increase in the tail width in the female DHT group is caused by an enlargement of the electrocytes in this area.Intracellular recordings from the electrocytes of saline and DHT injected females show a difference in the responses of the rostral faces of the electrocytes from the two groups, which reflect the differences in their EODs. Saline-treated animals had symmetrical EODs (the first and second phase of the EOD were equal in duration and amplitude), while the physiological responses from each face of the electrocytes yielded responses that were similarly equal in duration and amplitude. DHT-treated animals had asymmetrical EODs (the first phase of the EOD was similar to that of saline treated fish and larger in amplitude and shorter in duration than the second phase) and the physiological responses of the electrocytes reflected this asymmetry. The differential recordings across the caudal face were similar to those from saline treated fish, while the responses from the rostral face were longer in duration and smaller in amplitude.These data suggest that the effects of androgens underlie the changes in single electrocytes which produce the sexually dimorphic signals and morphology present in natural breeding populations ofHypopomus occidentalis.     

Electric organ discharges of the gymnotiform fishes: III. Brachyhypopomus

We measured and mapped the electric fields produced by three species of neotropical electric fish of the genus Brachyhypopomus (Gymnotiformes, Rham phichthyoidea, Hypopomidae), formerly Hypopomus. These species produce biphasic pulsed discharges from myogenic electric organs. Spatio-temporal false-color maps of the electric organ discharges measured on the skin show that the electric field is not a simple dipole in Brachyhypopomus. Instead, the dipole center moves rostro-caudally during the 1st phase (P1) of the electric organ discharge, and is stationary during the 2nd phase (P2). Except at the head and tip of tail, electric field lines rotate in the lateral and dorso-ventral planes. Rostro-caudal differences in field amplitude, field lines, and spatial stability suggest that different parts of the electric organ have undergone selection for different functions; the rostral portions seem specialized for electrosensory processing, whereas the caudal portions show adaptations for d.c. signal balancing and mate attraction as well. Computer animations of the electric field images described in this paper are available on web sites http://www.bbb.caltech.edu/ElectricFish or http://www.fiu.edu/∼stoddard/electricfish.html. Accepted: 22 September 1998     

Sodium-dependent plateau potentials in electrocytes of the electric fish <Emphasis Type="Italic">Gymnotus carapo</Emphasis>

The weakly electric fish Gymnotus carapo emits a triphasic electric organ discharge generated by muscle-derived electrocytes, which is modified by environmental and physiological factors. Two electrode current clamp recordings in an in vitro preparation showed that Gymnotus electrocytes fired repetitively and responded with plateau potentials when depolarized. This electrophysiological behavior has never been observed in electrocytes from related species. Two types of plateaus with different thresholds and amplitudes were evoked by depolarization when Na⁺-dependent currents were isolated in a K⁺- and Ca²⁺-free solution containing TEA and 4-AP. Two electrode voltage clamp recordings revealed a classical fast activating–inactivating Na⁺ current and two persistent Na⁺-dependent currents with voltage-dependencies consistent with the action potential (AP) and the two plateaus observed under current clamp, respectively. The three currents, the APs and the plateaus were reduced by TTX, and were absent in Na⁺-free solution. The different Na⁺-dependent currents in Gymnotus electrocytes may be targets for the modifications of the electric organ discharge mediated by environmental and physiological factors.     

Skeletal muscle transformation into electric organ in S. macrurus depends on innervation

The cells of the electric organ, called electrocytes, of the weakly electric fish Sternopygus macrurus derive from the fusion of mature fast muscle fibers that subsequently disassemble and downregulate their sarcomeric components. Previously, we showed a reversal of the differentiated state of electrocytes to that of their muscle fiber precursors when neural input is eliminated. The dependence of the mature electrocyte phenotype on neural input led us to test the hypothesis that innervation is also critical during formation of electrocytes. We used immunohistochemical analyses to examine the regeneration of skeletal muscle and electric organ in the presence or absence of innervation. We found that blastema formation is a nerve-dependent process because regeneration was minimal when tail amputation and denervation were performed at the same time. Denervation at the onset of myogenesis resulted in the differentiation of both fast and slow muscle fibers. These were fewer in number, but in a spatial distribution similar to controls. However, in the absence of innervation, fast muscle fibers did not progress beyond the formation of closely apposed clusters, suggesting that innervation is required for their fusion and subsequent transdifferentiation into electrocytes. This study contributes further to our knowledge of the influence of innervation on cell differentiation in the myogenic lineage.     

Magnetic and electric characteristics of the electric fish Gymnotus carapó.

The fresh water fish Gymnotus carapó produces a continuous series of weak pulsed electric fields in its surroundings and senses disturbances of this field as part of its sensory system. The electric and magnetic properties of the electric organ of this fish were studied. Magnetic fields close to the fish on the order of nT are produced by currents on the order of 10(-4) A in the electric organ of the fish. The electromotive force, the internal resistance, the current, and the electric power of the equivalent circuit were determined noninvasively.     

Morphological variation in the electric organ of the little skate (Leucoraja erinacea) and its possible role in communication during courtship

Skates discharge an electrical current too weak to be used for predation or defense, and too infrequent and irregular to be used for electrolocation. Additionally, skates possess a specialized sensory system that can detect electrical stimuli at the same strength at which they discharge their organs. These two factors are suggestive of a communicative role for the electric organ in skates, a role that has been demonstrated in similarly weakly electric teleosts (e.g., mormyrids and gymnotiforms). There is evidence that the sexual and ontogenetic variations in the electric organ discharge (EOD) in these other weakly electric fishes are linked to morphological variations in electric organs and the electrogenerating cells of the organs, the electrocytes. Little work has been done to examine possible sexual and ontogenetic variations in skate EODs or variations in the electrocytes responsible for those discharges. Electric organs and electrocyte morphology of male and female, and mature and immature little skates, Leucoraja erinacea, are characterized here. Female electric organs were bigger than male electric organs. This is suggestive of a sexually dimorphic EOD waveform or amplitude, which might be used as a sex-specific identification signal during courtship. The shapes of electrocytes that make up the organ were found to be significantly different between mature and immature individuals and, in some cases, posterior membrane surface area of the electrocytes increased at the onset of maturity due to the formation of membrane surface invaginations and papillae. This is evidence that the EOD of skates may differ in its waveform or amplitude or frequency between mature and immature skates, and act as a signal for readiness to mate. This study supports a communicative role during courtship for the weak electric organs of little skates, but studies that characterize skate EOD dimorphisms are needed to corroborate this speculation before conclusions can be drawn about the role the electric organ plays in communication during courtship.     

Oscillations of electric spatial patterns emerging from the homogeneous state in characean cells

Electric spatial patterns of bands formed along the cell wall of the characean internode were studied using a multi-electrode measuring system. The electric potential near the surface of the cell was measured by arranging about 25 electrodes along the cell at approximately 1.6 mm intervals. Since the time required for one scan over the cell length is only 1 s, the temporal change in the spatial pattern of surface electric potential can be readily observed. Oscillations were sometimes found as the electric pattern started to appear after the cell was illuminated. Fourier analysis shows that a single spatial mode arises gradually and then becomes stabilized in an oscillatory manner. A simple electric circuit model comprising three variables, i.e., a membrane potential, an electric current across the membrane and an electromotive force, can simulate well the oscillatory rise of bands. These results imply that the electric spatial pattern observed in characean internodes is a self-organized structure emerging far from equilibrium, known as a dissipative structure. Biophysical mechanisms of band formation are discussed.     

A field potential analysis of the electromotor system in Gymnotus carapo

To investigate the synchronization mechanisms operating in the electromotor system, electric organ discharge related field potentials of neural origin were recorded in intact fish. Components corresponding to the relay nucleus, the bulbar-spinal electromotor tract, the electromotoneurons and the peripheral nerves were identified. Delays between components were used to estimate the following intervals: (1) the conduction time along the cord (central conduction interval), (2) the interval between the local activation of the tract and the electromotoneuron firing within a restricted portion of the cord (coupling interval) and (3) the conduction time along the peripheral axons plus the time taken by synaptic activation of the electrocytes (peripheral interval). While central conduction interval increases with the distance from the pacemaker, the coupling interval diminishes. Peripheral interval also diminishes from rostral to caudal targets in the electric organ. It is concluded that the electrocyte synchronization, resulting from matching the three above-defined intervals, is achieved by a cascade of synergetic mechanisms.Abbreviations EBST electromotor bulbar-spinal tract - EMN electromotoneuron - EO electric organ - EOD electric organ discharge - PEN posterior electromotor nerve - PNA peripheral nerve activity - SFP skin surface field potentials     

Sound production to electric discharge: sonic muscle evolution in progress in Synodontis spp. catfishes (Mochokidae)

Elucidating the origins of complex biological structures has been one of the major challenges of evolutionary studies. Within vertebrates, the capacity to produce regular coordinated electric organ discharges (EODs) has evolved independently in different fish lineages. Intermediate stages, however, are not known. We show that, within a single catfish genus, some species are able to produce sounds, electric discharges or both signals (though not simultaneously). We highlight that both acoustic and electric communication result from actions of the same muscle. In parallel to their abilities, the studied species show different degrees of myofibril development in the sonic and electric muscle. The lowest myofibril density was observed in Synodontis nigriventris, which produced EODs but no swim bladder sounds, whereas the greatest myofibril density was observed in Synodontis grandiops, the species that produced the longest sound trains but did not emit EODs. Additionally, S. grandiops exhibited the lowest auditory thresholds. Swim bladder sounds were similar among species, while EODs were distinctive at the species level. We hypothesize that communication with conspecifics favoured the development of species-specific EOD signals and suggest an evolutionary explanation for the transition from a fast sonic muscle to electrocytes.     

Innervation pattern and electric organ discharge waveform in Gymnotus carapo (Teleostei; Gymnotiformes)

The electrogenic organ (EO) of Gymnotus carapo has two main portions: a posterior region consisting of four bilaterally arranged electrocyte rows; and an anterior portion composed of only two. The lateral row (LR) of the anterior portion contains doubly innervated electrocytes with axon terminals from different nerves on their rostral and caudal faces. The LR is continuous with the most dorsal row of the caudal region. This row also contains doubly innervated electrocytes. The medial row (MR) electrocytes of the anterior region and ventral rows of the caudal region are exclusively caudally innervated. All caudal faces of the anterior or abdominal region are supplied by two nerves which originate from spinal roots VIII to XXI. Roots I to VII give origin to pure rostral nerves whose electromotor axons terminate on the rostral surfaces of the first seven LR electrocytes. A given doubly innervated electrocyte is supplied on its caudal face by a nerve originating several segments (usually seven) posterior to the spinal root supplying its rostral face. Transections of the spinal cord at the level of root VIII isolate the activity of the rostral surfaces of the first electrocytes. The EO discharge (EOD) then appears as a head negative deflection which arises from abdominally located electrocytes. Its monophasic character reveals that the activity remains restricted to the rostral electrocyte surfaces. Damage of the abdominal portion of the EO abolishes the first negative deflection of the normal pulse. Transections of the spinal cord at the level of root XXI isolate the activity of the whole abdominal portion of the EO. Since both doubly and singly innervated electrocytes remain active, the EOD appears biphasic. Comparative studies have shown that the EOD of Hypopomus sp. lacks any early negative wave and correspondingly all its electrocytes are exclusively caudally innervated.     

Cytoembryologic aspects of evolution of specialized electric organs of fishes

Almost all fish electric organs (EO) developed from the skeletal muscles or from its embryonic rudiments. The only exception is the definite (in contrast to larval) EO of Apteronotidae, formed by motoneurons, whose loss of relation with muscles is secondary. The main feature of all EO of the muscle genesis is cooperative morphological and electrophysiological polarity of their electrocyte cells anterioposteriorly or (in Torpedo, Uranoscopus) of the dorso-ventral axes of the body. In particular, for the EO of muscular origin, unilateral asymmetric innervation of electrocytes by electromotoneurons is characteristic. Such innervation is a prerequisite condition for the summation of electric discharges. It is one of the main distinctions of EO from definitive skeletal muscles. However, in the emryogenesis of all vertebrates the initial innervation of muscle rudiments by the so-called pioneer motoneurons occurs. In teleosts (according to data on Brachidanio rerio available) extending to every myotome are outgrowths of three pioneer motoneurons referred to after their position in the nerotubule as "rostral", "medial" and "caudal". The former two innervate dorsally with the dorsal compartment of the myotome. The third approaches the ventral compartment of the same myotome caudally. In the gymnotic fish the innervation of EO formed from the axial skeletal muscles retains the same nature. The electrocytes of EO from the dorsal and ventral compartments of the myotome, are approached by electromotoneurons, respectively, rostrally and caudally. In compartments, the antipolarity of the innervation of the dorsal and ventral EO compartments leads to a paradoxical effect of generation of anti-polar pulses. The summation of these pulses creates a very short difference electric charge. In Mormyridae the antipolarity of the innervation of the rostral and ventral compartments of EO formed from the axial muscle is not pronounced. However, electroneurons resemble pioneer motoneurons by the following characters: the large size of the bodies and their localization near the central tube, absence of dendrities, electrosynaptic connection, polar (asymmetrical) pattern of electrocyte innervation. Outside EO, the cooperative polarity of the cells is only characteristic of epithelia, particularly, ciliated. At the same time, in some electric fish, the electrogeneratory tissue is similar to epithelium in a number of morphological characters, or the genes expressed in it show the gene of keratin AE-1, typical of epithelia. The above gives grounds to believe that EO of muscle origin are a product of fixation and aggravation by natural selection of hereditary anomalies, manifested in the recovery or in the retaining of the embryonic (i.e., polar nature) of the efferent innervation of some parts of skeletal muscles. Another distinction of EO from the muscles appears to lie in the expression of some individual components of the gene epithelial complex. A method is proposed for electromyographic recording of such anomalies and molecular-genetic approachers to analysis of their nature. The causes of the absence of EO epithelial genesis are discussed and also of the fact that these organs developed only in the evolution of fish.