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The development of swimming was investigated in zebrafish aged 1.5 to 5 days postfertilization by examining both the swimming behavior and its generation by the nervous system. Upon hatching (at day 2), swimming is undirected and occurs in sustained bursts of high frequency (mean = 67 Hz) tail undulations. By 4 days, the swimming pattern matures to a more directed, less erratic, beat-and-glide pattern where slower (mean = 35 Hz) tail undulations, lasting ∼200 ms, alternate with longer gliding rest periods. Swimming is powered by two classes of embryonic muscles (embryonic red, ER and white, EW) that are electrically coupled within (but not between) classes and have physiological properties similar to vertebrate tonic and twitch muscle, respectively. ER fibers have a lower chloride ion permeability than EW fibers and do not have sodium dependent action potentials. In paralyzed preparations, motoneurons and muscle fibers received coordinated excitatory synaptic activity (with left to right alternation and head to tail propagation) corresponding to either burst or beat-and-glide swimming. ER muscle was de-recruited at the fastest swimming rates and EW fibers dropped out at the slowest swimming rates. Rhythmic motoneuron output was generated by a phasic glutamatergic and a largely tonic glycinergic synaptic drive. Glutamatergic synapses had either or both AMPA/kainate and NMDA receptors and the kinetics of these synaptic currents were fixed throughout the developmental period examined. When depolarized, motoneurons fired high frequency (up to 800 Hz) bursts of action potentials that rapidly accommodated (within ∼20 ms) due to voltage and calcium dependent outwardly rectifying conductances. These intrinsic motoneuron properties are hypothesized to interact with the rhythmic synaptic drive to pattern motor output (at ∼25--75 Hz) to locomotor muscles. The neural generation of swimming in developing zebrafish is thus fundamentally similar to locomotion in adu

Superior swimming stamina in adult fish is presumably passed on to their offspring, but the ontogeny of the appearance of superior stamina and the requisite enhanced cardio-respiratory support for locomotion in larval fishes has not been determined. Is the expression of the suite of parental traits enabling superior swimming stamina in their offspring dependent upon their achieving juvenile/adult morphology, or does it appear earlier in their larvae? To answer this, adults were classified into three groups based on swimming stamina, followed by measurement of length, mass, and width. Larval offspring from the two parental groups -high stamina larvae (HSL) and low stamina larvae (LSL)- were reared at 27°C in aerated water (21% O2). Routine and active heart rate, routine and active mass specific oxygen consumption were recorded through 21dpf, and cost of transport (COT) and factorial aerobic scope were derived from oxygen consumption measurements. Routine heart rate at 2dpf of LSL was 164 ± 1 b·min-1, compared to only 125 ± 2 b·min-1 for HSL. Routine heart rate subsequently peaked at 203 ± 1 b·min-1 at 5dpf in the HSL group, compared to 207 ± 1 b·min-1, at 4dpf in the LSP larvae. Active heart rate at 5 dpf of LSL was 218 ± 2 b·min-1 compared to 216 ± 2 b·min-1 for HSL. Active heart rate increased slightly to 227 ± 2 b·min-1 for LSL before decreasing again, while active heart rate remained relatively constant for HSL. Routine O2 consumption at 2dpf of HSL was 0.09 μmol·mg-1·hr-1, compared to 0.03 μmol·mg-1·hr-1 in LSL. Routine O2 consumption subsequently peaked at 0.70 μmol·mg-1·hr-1 at 9dpf in the HSL, compared to 0.71 μmol·mg-1·hr-1, at 9dpf in the LSL. These values dramatically decreased before leveling off at around 0.20 μmol·mg-1·hr-1 and 0.15 μmol·mg-1·h-1, respectively. Active O2 consumption at 5dpf for HSL was 0.38 μmol·mg-1·hr-1, compared to 0.57 μmol·mg-1·hr-1 for LSL. Active O2 consumption subsequently peaked at 0.97 μmol·mg-1·hr-1 at 10dpf in HSL, compared to 1.19 μmol·mg-1·hr-1 at 7dpf in LSL. These values also dramatically decreased and leveled off. Significant differences (p < 0.05) in heart rate and oxygen consumption persisted through 21dpf. The onset of differences observed in routine and active heart rate in early larvae, correlated with parent stamina, show that juvenile or adult features are not required as a precondition for the emergence of phenotypic physiological differences.