The influence of neural activity on the morphology of retinal-axon-terminal arbors and the precision of the developing retinotectal projection in zebrafish embryos was explored. Terminal-arbor morphology and their distribution in the tectum was determined with anatomical fiber-tracing methods using the fluorescent dyes dil and diO. To allow development under activity-deprived conditions, TTX was injected into the eyes of 30-38-hr-old zebrafish embryos at concentrations that effectively blocked neural activity both in retinal ganglion cells and throughout the CNS. Much like axons with normal neural-activity patterns, activity-deprived axons from dorsal and ventral and from temporal and nasal regions in the retina terminated over retinotopically appropriate and nonoverlapping regions of the tectum. Even after ablation of 1 hemiretina at the time of axonal outgrowth, activity-deprived axons from the remaining hemiretina grew directed toward and arborized selectively within their retinotopically appropriate tectal half in the same way as would nondeprived axons. Besides being retinotopic, the area over which small populations of activity-deprived axons from neighboring ganglion cells arborize is as small as that of active axons. The size of terminal arbors of retinal ganglion cell axons was unaffected by blockade of neural activity. The mean terminal-arbor size was 27 x 18 microns for the TTX-injected and 31 x 22 microns for the control embryos. The tectal coverage of TTX-blocked and control axons was equally small, with values of 1.4% and 1.6%, respectively. These data show that a precisely organized retinotopic map in developing zebrafish forms independent of neural-impulse activity.

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In cichlid, poecilid and centrarchid fishes luteinizing hormone releasing hormone (LHRH)-immunoreactive neurons are found in a cell group (nucleus olfactoretinalis) located at the transition between the ventral telencephalon and olfactory bulb. Processes of these neurons project to the contralateral retina, traveling along the border between the internal plexiform and internal nuclear layer, and probably terminating on amacrine or bipolar cells. Horseradish peroxidase (HRP) injected into the eye or optic nerve is transported retrogradely in the optic nerve to the contralateral nucleus olfactoretinalis where neuronal perikarya are labeled. Labeled processes leave this nucleus in a rostral direction and terminate in the olfactory bulb. The nucleus olfactoretinalis is present only in fishes, such as cichlids, poecilids and centrarchids, in which the olfactory bulbs border directly the telencephalic hemispheres. In cyprinid, silurid and notopterid fishes, in which the olfactory bulbs lie beneath the olfactory epithelium and are connected to the telencephalon via olfactory stalks, the nucleus olfactoretinalis or a comparable arrangement of LHRH-immunoreactive neurons is lacking. After retrograde transport of HRP in the optic nerve of these fishes no labeling of neurons in the telencephalon occurred. It is proposed that the nucleus olfactoretinalis anatomically and functionally interconnects and integrates parts of the olfactory and optic systems.

We investigated the filter properties of the highly branched trunk lateral lines of the stichaeid Xiphister atropurpureus and compared them to the filter properties of simple lateral line canals. For this purpose artificial canals were constructed, some of which were fitted with artificial neuromasts. In still water, the response of a simple canal versus two types of Xiphister-like canals to a vibrating sphere stimulus were similar, as was the decrease in the responses as a function of sphere distance. Also comparable was the mechanical coupling between neighboring parts of the main canal. However, compared to the simple canal, the Xiphister-like canals showed a lower spatial resolution. Equipping artificial lateral line canals with artificial neuromasts revealed that Xiphister-like canals, i.e., lateral lines canals with tubuli that contained widely spaced pores, improve the signal-to-noise ratio in a highly turbulent environment. Even though a reduced spatial resolution is the price for this improvement, Xiphister may compensate for this compromise by having four instead of the usual single trunk lateral line canal. We suggest that lateral line canals with tubuli that contain widely spaced pores and multiple lateral line canals on each body side are an adaptation to a highly turbulent aquatic environment.

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The activities of single afferent fibers were recorded in the trunk lateral line nerve of the cichlid fish Sarotherodon niloticus L. Using both electrophysiological recordings and neuroanatomical tracing techniques, the number, arrangement, and innervation of superficial (SNs) and canal (CNs) neuromasts were determined. Both, SNs and CNs, are innervated by several afferent fibers of different diameters and efferent fibers. The CNs and SNs are neuronally separated: afferent fibers which innervate both CNs and SNs were not found. Whereas the single CN is innervated by a separate set of afferent fibers, fibers innervating the SNs within rows often branched to reach all or several SNs. The SNs within a row were thus considered to form a functional unit. With the exception of SNs on the tail fin, functional units of neuromasts were in general topographically restricted to single scales.The majority of lateral line units had resting activity. On the basis of the time interval distribution of the resting activity, 4 types of units were classified: these were labelled irregular (type I), regular (type II), bimodal (type III) and silent (type IV). Type I was the most common type of resting activity (obtained in 47.8% of the recorded units). Units with this resting activity type were identified as afferents innervating either SNs or CNs. Units with resting activity of type II represented mostly afferents of CNs if their mean activity was high (around 40 imp/s). If the mean activity of this type was below 20 imp/s the units were unresponsive to local water movements and at least some were identified as efferent fibers. Resting activity of type III was found only in units originating from CNs. Only 4% of the units were silent (type IV). These units were often identified as injured neuromasts.Abbreviations." SN superficial neuromast; CN canal neuromast Units originating from CNs show higher mean resting activity than those from SNs. For both SN and CN units, the mean discharge rate of the resting activity correlated with the sensitivity to stimulation for sinusoidal water movements.During stimulation of the neuromasts by sinusoidal water movements of small amplitude and different frequencies, the response characteristics of SN and CN units were determined by linear frequency analysis under steady state conditions. Most units responded linearly to small stimulus amplitudes. In this amplitude range the units' resting activity was modulated according to the stimulus frequency. Small stimulus amplitudes proportionally changed the amount of modulation but did not alter the phase of the response. CN and SN units that responded linearly produce differing frequency responses. Whereas CNs were most sensitive at frequencies of up to 200 Hz (center frequencies between 100 and 200 Hz), the center frequencies of SNs were distributed between 10 and 70 Hz with a maximum number at about 30 Hz. Bode plots for many CN and SN units indicated that the neuromasts were sensitive to the acceleration component of the water movement.The functional si...

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