Sex differences in the waveform of the pulse-type electric fish,Pollimyrus isidori (Mormyridae)

Summary This paper reports the finding of a sexual dimorphism in the electric organ discharge of the weakly electric fishPollimyms isidori. The difference in the head-positive components of the waveform (Fig. 1) was found in 95% of adults. Juvenile fish always possessed female type discharges. Fourier analysis (Fig. 3) revealed significant sex differences in the power spectra of the discharges, indicating that specific phase information is perhaps unnecessary for sexual identification. The results are discussed with reference to our current knowledge of coding of electrocommunication signals in the electrosensory system.Abbreviation EOD electric organ discharge     

Reproduction and development of the weakly electric fish,Pollimyrus isidori (Mormyridae,Teleostei) in captivity

Synopsis No clear sexual dimorphism occurs in Pollimyrus isidori. Females usually grew slightly larger than males. The anal-fin reflex, however, makes it easy to discriminate between males and females. Spawning took place during the first six hours of the dark phase, in the territory of the male. During each spawning act 2–4 eggs were laid. The male put the eggs into a well-hidden nest previously constructed from plant material. The eggs, free embryos, and larvae of several spawnings were guarded by the male for several weeks. The females laid on average 120 eggs per fractional spawning. The eggs were 2 mm in diameter, not adhesive and very yolky. There was a relationship between pH and viability (% embryos hatched). Hatching occurred on the third day after spawning. The respiratory network of segmental origin in the median fin fold was well developed in the free embryos. Transition to exogenous feeding occurred on day 14. The larval period ended when the fish were 15 mm long and 40–50 days old. First gonadal recrudescence occurred at a total length of 6 cm (about 200 days old). The environmental factors decreasing conductivity and pH, increasing water level, and imitation of rain led to gonadal recrudescence, but pH did not act as a cue. Recrudescence was triggered by a decrease of conductivity, but absolute values or ionic composition of the water were not important. Maturation was completed after about fifty days. Mature and spawning fish no longer required any variation of these environmental factors to maintain mature gonads. A steady and considerable increase in conductivity led to gonadal regression. The fish did not show postbreeding refractoriness.     

On the electromotor neurons of both electric organs of Pollimyrus isidori (Mormyridae, Teleostei)

The electromotor neurons (EMNs) of the adult electric organ of Pollimyrus isidori and the "giant neurons" (GNs) found in the more rostral part of the spinal cord were investigated both with light and electron microscopical methods. The two kinds of neuron are more or less similar in size, about 30 microns, and are found in the more dorsal part of the spinal cord. The EMNs show somatosomatic gap junctions, as do the GNs. In addition, chemical synapses could be found between nerve fibres and both types of neurons. Histochemical investigations show that the EMNs and the GNs are both AChE positive. On the basis of the arguments presented in the discussion, we believe that the "giant neurons" are the electromotor neurons of the larval electric organ of Pollimyrus isidori.     

Central auditory neurophysiology of a sound-producing fish: the mesencephalon of Pollimyrus isidori (Mormyridae)

This paper describes the auditory neurophysiology of the mesencephalon of P. isidori, a soundproducing mormyrid fish. Mormyrids have a specialized pressure-sensitive auditory periphery, and anatomical studies indicate that acoustic information is relayed to the mesencephalic nucleus MD. Fish were stimulated with tone bursts and clicks, and responses of MD neurons were recorded extracellularly. Auditory neurons had best frequencies (BF) and best sensitivities (BS) that fell within the range of frequencies and levels of the natural communication sounds of these fish. BSs were in the range of 0 to — 35 dB (re. 1.0 dyne/cm²). Many of the neurons were tuned (Q_{10 dB}: 2–6), and had BFs in the range of 100–300 Hz where the animal's sounds have their peak energy. A range of different physiological cell types were encountered, including phasic, sustained, and complex neurons. Some of the sustained neurons showed strong phase-locking to tones. Many neurons exhibited non-monotonic rate-level functions. Frequencies flanking the BF often caused a reduction in spontaneous activity suggesting inhibition. Many neurons showed excellent representation of click-trains, and some showed a temporal representation of inter-click-intervals with errors less than 1 ms.Abbreviations BF best frequency - BS best sensitivity - ELa anterior exterolateral toral nucleus - ELp posterior exterolateral toral nucleus - EOCD electric organ command discharge - FFT fast Fourier transform - HRP horseradish peroxidase - ICI inter-clickinterval - MD mediodorsal toral nucleus (=auditory nucleus) - OR onset response rate - PSTH peri-stimulus-time-histogram - R synchronization coefficient - RA response area - SS steady state response rate     

Trained Weakly-electric Fishes Pollimyrus isidori and Gnathonemus petersii (Mormyridae,Teleostei) Discriminate between Waveforms of Electric Pulse Discharges

Fish of the family Mormyridae emit weak, pulse-like electric organ discharges (EODs). The discharge rhythm is variable, but the waveform of the EOD is constant for each fish, with species- and individual characteristics. The ability of Pollimyrus isidori and Gnathonemus petersii (Mormyridae) to discriminate between different EOD waveforms was tested using a differential conditioning procedure. Fish were first trained to respond to a reference signal in swimming to a dish to receive a bloodworm (food reward). The reference signal consisted of a 10-Hz train of the digitally recorded EOD of a conspecific. Second, an alternative signal (10-Hz train of a different EOD, either from another species, or from a conspecific of the other sex) was associated with air bubbles as punishment. The two signals were played at successive trials in random order. On each trial the latency was measured between the onset of the signal and the response. 7 out of the 8 P. isidori tested and both of the two G. petersii tested associated the reference EOD with food. Among these, five P. isidori and two G. petersii responded differentially (p < 0.01) to EODs of different species. P. isidori similarly discriminated between conspecific EODs of different sexes. The quantity of different alternative EODs which could be tested was limited when fish eventually habituated to the punishment. Even when the amplitude of the EODs was randomly changed at each trial, two out of two G. petersii differentiated between EODs of the two species, and three out of three P. isidori tested differentiated between EODs within their own species. Response latencies to the rewarded signal during the basic training and during discrimination (when it had to be distinguished from the S-) were similar. G. petersii showed differential responses for S+ and S- also in the rhythm of discharge exhibited during playback, after five EOD pulses for one fish, and after a single pulse for the other. Mormyrids may therefore distinguish between conspecifics and members of other species, and even between individual conspecifics, by their EOD waveform.     

The anal fin complex in a weakly discharging electric fish, Gnathonemus petersii(Mormyridae)

An examination of the permanent bony structures of the anal fin complex in the mormyrid fish, Gnathonemus petersii , revealed two new structural sexual dimorphisms: longer proximal pterygiophores and wider anal fin rays in males than in females. Both structures are thought to facilitate the male's courtship‐associated anal fin reflex. Adult male mormyrid fishes are characterized by a dorsally directed indentation of the posterior body wall (anal fin indentation). The expression of this indentation in males, presumably driven by anal fin musculature, was correlated with the fish's gonadal state: large indentations were associated with high gonado‐somatic indices and small indentations with low indices.     

Development of the gigantocerebellum of the weakly electric fish Pollimyrus

The morphogenesis of the "hypertrophied" mormyrid cerebellum was investigated in Pollimyrus (Pisces). Two adults and 36 larvae and young fish raised in captivity were used. Two Gnathonemus petersii adults were taken for comparison. The ontogenetic development of the various cerebellar structures was analysed in inverse chronological order with the aid of serial sagittal and frontal brain sections. Special attention was given to the trilobed corpus cerebelli (C1, C2, C3), the lobi transitorii et caudales, the valvula, the crista cerebelli, the eminentia granularis and the lobus lineae lateralis. 1. The cerebellar structures are of bilateral origin; they develop from the cerebellar and acoustico-lateral "anlage" of the rhombencephalon behind the rhombomesencephalic fissure, either through budding or individualisation and appear between the 4th and 11th day after spawning. The midline fusion of the symmetrical structures is accomplished somewhat later, between the 8th and 23rd days. 2. The cerebellar structures acquire their definitive spatial organisation within 38 days, except for the valvula whose development takes much longer. Recognisable from the 11th day, the valvula upon which ridges are visible from the beginning continues to grow after the 38th day beyond the mesencephalic ventricle, finally overlying the telencephalon frontally and the different rhombencephalic structures caudally. This development, which includes a large antero-lateral folding of the valvula, takes 240 days. 3. Cytological differentiation is just as complex as the general development of the cerebellar structures. Cortical stratification first begins on the 8th to the 11th day in the corpus cerebelli and in the valvula from day 21 to 23 onwards. This differentiation is characterised throughout almost the entire cerebellum by a downward migration of the superficial undifferentiated cells which then constitute the granular layer. In the valvula, the majority of the undifferentiated cells leave the ridges to form a continuous granular layer at the base of the ridges. 4. A differentiation gradient was observed on the antero-posterior axis. 5. In spite of its complexity, the mormyrid cerebellum develops much more rapidly than the cerebellum of the trout.     

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.     

Differentiation of morphology, genetics and electric signals in a region of sympatry between sister species of African electric fish (Mormyridae)

Mormyrid fishes produce and sense weak electric organ discharges (EODs) for object detection and communication, and they have been increasingly recognized as useful model organisms for studying signal evolution and speciation. EOD waveform variation can provide important clues to sympatric species boundaries between otherwise similar or morphologically cryptic forms. Endemic to the watersheds of Gabon (Central Africa), Ivindomyrus marchei and Ivindomyrus opdenboschi are morphologically similar to one another. Using morphometric, electrophysiological and molecular characters [cytochrome b sequences and amplified fragment length polymorphism (AFLP) genotypes], we investigated to what extent these nominal mormyrid species have diverged into biological species. Our sampling covered the known distribution of each species with a focus on the Ivindo River, where the two taxa co-occur. An overall pattern of congruence among datasets suggests that I. opdenboschi and I. marchei are mostly distinct. Electric signal analysis showed that EODs of I. opdenboschi tend to have a smaller initial head-positive peak than those of I. marchei, and they often possess a small third waveform peak that is typically absent in EODs of I. marchei. Analysis of sympatric I. opdenboschi and I. marchei populations revealed slight, but significant, genetic partitioning between populations based on AFLP data (F(ST) approximately 0.04). Taken separately, however, none of the characters we evaluated allowed us to discriminate two completely distinct or monophyletic groups. Lack of robust separation on the basis of any single character set may be a consequence of incomplete lineage sorting due to recent ancestry and/or introgressive hybridization. Incongruence between genetic datasets in one individual, which exhibited a mitochondrial haplotype characteristic of I. marchei but nevertheless fell within a genetic cluster of I. opdenboschi based on AFLP genotypes, suggests that a low level of recent hybridization may also be contributing to patterns of character variation in sympatry. Nevertheless, despite less than perfect separability based on any one dataset and inconclusive evidence for complete reproductive isolation between them in the Ivindo River, we find sufficient evidence to support the existence of two distinctive species, I. opdenboschi and I. marchei, even if not 'biological species' in the Mayrian sense.     

Basal expansion of anal-fin rays: a new osteological character in weakly discharging electric fish (Mormyridae)

Bone expansion of anal-fin rays in mormyrid fish is introduced as a new osteological character to distinguish two mormyrid species, Brienomyrus brachyistius from Nigeria and Brienomyrus kingsleyae from Gabon. This character is sexually dimorphic and species-specific, affecting the bases of anal-fin rays in adult males only. Between the two species, it differed in degree, the number of rays involved, and the number of the first ray affected. These differences together with differences in conventional meristic and morphometric characters further support ongoing revisions of Brienomyrus taxonomy.     

Eighteen microsatellite loci for endemic African weakly electric fish (Campylomormyrus,Mormyridae) and their cross species applicability among related taxa

We describe isolation and characterization of the first microsatellite loci specifically developed for African weakly electric fish (Mormyridae), for the genus Campylomormyrus. Seventeen of our 18 loci are polymorphic within the Campylomormyrus numenius species complex. The polymorphic loci showed four to 15 alleles per locus, an expected heterozygosity between 0.46 and 0.94, and an observed heterozygosity between 0.31 and 1.00. Most primers also yield reproducible results in several other mormyrid species. These loci comprise a set of molecular markers for various applications, from moderately polymorphic loci suitable for population studies to highly polymorphic loci for pedigree analysis in mormyrids.     

Petrocephalus boboto and Petrocephalus arnegardi,two new species of African electric fish (Osteoglossomorpha,Mormyridae) from the Congo River basin

A specimen of the African weakly electric fish genus Petrocephalus (Osteoglossomorpha, Mormyridae) collected in the Congo River at Yangambi, Orientale Province, Democratic Republic of Congo, is described as a new species. Petrocephalus boboto sp. n. can be distinguished from other Central African species of Petrocephalus by a combination of the following characteristics: three distinct black spots on the body, one at the origin of the pectoral fin, one at the origin of the caudal fin and one below the anterior base of the dorsal fin; Nakenrosette and Khelrosette electroreceptor clusters distinct on head but Augenrosette cluster reduced in size; 23 branched dorsal rays, 34 branched anal rays, and electric organ discharge waveform triphasic. Petrocephalus boboto sp. n. most closely resembles the holotype of Petrocephalus binotatus but is easily distinguished from it by its smaller mouth. A comparative molecular analysis including 21 other Petrocephalus species shows Petrocephalus boboto sp. n. to be genetically distinctive and to represent a deep lineage in the genus. Two specimens of Petrocephalus collected at Yangambi are morphologically similar and genetically closely related to specimens previously assigned to Petrocephalus binotatus, collected in the northwestern Congo River basin within Odzala-Kokua National Park, Republic of the Congo. This prompts us to formally describe a new species from these collections, Petrocephalus arnegardi sp. n., that, although similar to the holotype of Petrocephalus binotatus, can be distinguished from it by its smaller mouth and shorter interorbital width.