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Dev Neurobiol
2010 Nov 01;7013:862-74. doi: 10.1002/dneu.20822.
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Sexually distinct development of vocal pathways in Xenopus laevis.
Yamaguchi A
,
Muñoz MM
,
Bose TO
,
Oberlander JG
,
Smith S
.
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Deterministic rules, rather than experience, are thought to regulate the development of simple behaviors in vertebrates and invertebrates. We revisited this issue through examination of the sexually distinct vocalizations of African clawed frogs (Xenopus laevis), a reproductive behavior used by sexually mature males and females. We discovered that, as expected for simple behavior, female vocalizations develop through deterministic rules. The rare calls of juvenile females are indistinguishable from those of adult females. The vocal pathways of juvenile females, as measured by the contractile properties of the laryngeal muscles (the vocal muscles) and the laryngeal motoneuron somata (vocal motoneurons) size, are the developmental default and do not differentiate as they mature. Male Xenopus, in contrast, produce extensive vocalizations with rudimentary acoustic structure before reaching sexual maturity. Moreover, the functional properties of the vocal central pattern generator mature before muscle fibers and motoneuron size are fully masculinized. The results suggest that neuronal activity during development may be important in organizing the contractile properties of the muscle fibers in male, but not in female Xenopus.
Figure 1. Vocal development in male and female Xenopus. AâG: Normalized frequency histograms of instantaneous click rates obtained from adult females (A), juvenile females (B), juvenile males (all animals combined, C), Group I juvenile males (D), Group II juvenile males (E), Group III juvenile males (F), adult males (G). HâM: Sound spectrograms of calls recorded from an adult female (H), juvenile female (I), Group I juvenile male (J), Group II juvenile male (K), Group III juvenile male (L), and adult male (M).
Figure 2. Body mass of juvenile males is a poor predictor of vocal maturity. Bivariate plots of maximum instantaneous click rates (top) and maximum sustained click rates (bottom) as a function of body mass. Note that there is no association between click rates and body mass. The range of body weight for each juvenile group is indicated with a horizontal bar with double arrows in the bottom.
Figure 3. Sound spectrograms of advertisement calls produced by adult males and juvenile Group III males. Dotted line indicates the onset of fast trills. Arrows indicate the silent intervals found at the end of the fast trills in all juvenile males.
Figure 4. Fictive advertisement calls produced by adult and juvenile male brains. Shaded boxes indicate fast trills in each call. Note that there are no silent intervals (see Fig. 3). In fictive advertisement calls of juvenile males.
Figure 5. Contractile properties of adult and juvenile laryngeal muscles. A: Contractile force recorded from a laryngeal muscle in response to repetitive stimulation delivered to the laryngeal nerve. B: Slope to peak tension and halfârelaxation time were measured from the tension profile elicited in response to a single shock delivered to the nerve. C: Proportion of fused tension produced in response to stimuli delivered at 10, 30, 50, and 70 Hz by larynges obtained from adult females, juvenile females, juvenile males, and adult males. D, E: Cell plots of tension slope (D) and half relaxation time (E). Error bars indicate standard errors. Asterisks in C, D, and E indicate significant differences, and ân.s.â indicates not significant difference. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]
Figure 6. Size of laryngeal motoneuron somata. A: Cell plots of somata size obtained from adult and juvenile males and females. Error bars indicate standard errors. B: Regression plot of mean somata volume as a function of body mass. Four groups of animals (adult and juvenile males and females) are color coded as in A. C: Bivariate plot showing the somata volume as a function of body mass. Color coding scheme is the same as in A. Adult males do not have small sized motoneurons, indicated by dotted line.
Doupe,
Birdsong and human speech: common themes and mechanisms.
1999, Pubmed
Doupe,
Birdsong and human speech: common themes and mechanisms.
1999,
Pubmed
Fleshman,
Rheobase, input resistance, and motor-unit type in medial gastrocnemius motoneurons in the cat.
1981,
Pubmed
Gundersen,
Determination of muscle contractile properties: the importance of the nerve.
1998,
Pubmed
Hamburger,
Periodic motility of normal and spinal chick embryos between 8 and 17 days of incubation.
1965,
Pubmed
Hanson,
Characterization of the circuits that generate spontaneous episodes of activity in the early embryonic mouse spinal cord.
2003,
Pubmed
Kelley,
Neuroeffectors for vocalization in Xenopus laevis: hormonal regulation of sexual dimorphism.
1986,
Pubmed
,
Xenbase
Knörnschild,
Complex vocal imitation during ontogeny in a bat.
2010,
Pubmed
Komuro,
Orchestration of neuronal migration by activity of ion channels, neurotransmitter receptors, and intracellular Ca2+ fluctuations.
1998,
Pubmed
Konczak,
The development of goal-directed reaching in infants: hand trajectory formation and joint torque control.
1995,
Pubmed
Moody,
Ion channel development, spontaneous activity, and activity-dependent development in nerve and muscle cells.
2005,
Pubmed
Potter,
Androgen-induced vocal transformation in adult female African clawed frogs.
2005,
Pubmed
,
Xenbase
Rhodes,
Xenopus vocalizations are controlled by a sexually differentiated hindbrain central pattern generator.
2007,
Pubmed
,
Xenbase
Ruedi,
Age, but not experience, affects courtship gene expression in male Drosophila melanogaster.
2009,
Pubmed
Saint-Amant,
Time course of the development of motor behaviors in the zebrafish embryo.
1998,
Pubmed
Shatz,
Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents.
1988,
Pubmed
Tobias,
Vocal communication between male Xenopus laevis.
2004,
Pubmed
,
Xenbase
Tobias,
Rapping, a female receptive call, initiates male-female duets in the South African clawed frog.
1998,
Pubmed
,
Xenbase
Tobias,
Vocalizations by a sexually dimorphic isolated larynx: peripheral constraints on behavioral expression.
1987,
Pubmed
,
Xenbase
Wetzel,
Androgen and gonadotropin effects on male mate calls in South African clawed frogs, Xenopus laevis.
1983,
Pubmed
,
Xenbase