THE ONTOGENY OF INTERSEXUAL AND INTRASEXUAL VOCAL MUSCLE DIMORPHISMS IN A SOUND-PRODUCING FISH

被引:60
作者
BRANTLEY, RK [1 ]
TSENG, J [1 ]
BASS, AH [1 ]
机构
[1] UNIV CALIF BODEGA BAY, BODEGA MARINE LAB, BODEGA BAY, CA USA
关键词
SEXUAL DIMORPHISM; ALTERNATIVE REPRODUCTIVE TACTICS; PEDOMORPHOSIS; PROGENESIS; HETEROCHRONY; TELEOST;
D O I
10.1159/000114170
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
This study documents the development of inter- and intrasexual dimorphisms in the vocal ('sonic') muscles of the swimbladder in the plainfin midshipman fish, Porichthys notatus. Midshipman have two male reproductive morphs, Types I and II. Only Type I males build nests and generate mate calls to attract females; Type II males sneak or satellite spawn. Vocal muscles in the mate-calling Type I males were 25-fold larger in absolute size (sixfold larger when scaled to body size) compared with females or non-calling Type II males. Dimorphisms in muscle mass were correlated with dimorphisms in fiber number and diameter. Only nascent Type I males experienced a pre-maturational, fourfold increase of fiber number followed by a rapid, fivefold increase in fiber cross-sectional area at sexual maturity. Also specific to Type I males was a striking change in cell structure: the ratio of sarcoplasm to myofibril area increased fivefold. By contrast, Type II males and females matured without showing any of these changes in sonic muscle - the the trajectories which described juvenile growth continued to hold through maturity and adulthood. The results indicate distinct, non-sequential, ontogenetic trajectories for Type I and Type Il males. The origin of the Type II male morphotype is described as paedomorphosis by progenesis: size distributions of free-living animals suggest that Type II males can mature precocially as one-year-old fish, whereas Type I males defer reproduction until they are at least two years of age.
引用
收藏
页码:336 / 349
页数:14
相关论文
共 59 条
[1]  
Arnold A.P., Gorski H.A., Gonadal steroid induction of structural sex differences in the central nervous system, Ann. Rev. Neurosci, 7, pp. 413-444, (1984)
[2]  
Bass A.H., Evolution of vertebrate motor systems for acoustic and electric communication: Peripheral and central elements, Brain Behav. Evol, 33, pp. 237-247, (1989)
[3]  
Bass A.H., Sounds from the intertidal zone: ‘vocalizing' fish, Bioscience, 40, pp. 247-258, (1990)
[4]  
Bass A.H., Dimorphic male brains and alternative reproductive tactics in a vocalizing fish, Trends Neurosei, 15, pp. 139-145, (1992)
[5]  
Bass A.H., Andersen K., Intra- and Inter-sexual dimorphisms in the sound generating motor system in a vocalizing fish: Motor axon number and size, Brain Behav. Evol, 57, pp. 204-214, (1991)
[6]  
Bass A.H., Baker R., Sexual dimorphisms in the vocal control system of a teleost fish: Morphology of physiologically identified neurons, J. Neurobiol, 21, pp. 1155-1168, (1990)
[7]  
Bass A.H., Baker R., Evolution of homologous vocal control traits, Brain Behav. Evol, 58, pp. 240-254, (1991)
[8]  
Bass A.H., Marchaterre M.A., Soundgenerating (sonic) motor system in a teleost fish (Porichthys notatus): Sexual polymorphism in the ultrastructure of myofibrils, J. Comp. Neurol, 256, pp. 141-153, (1989)
[9]  
Billon H.T., Alderdice D.F., Schnute J.T., Influence of time and size at release of juvenile coho salmon (Oncorhynchus kisutch) on returns at maturity, Can. J. Fish. Aq. Sci, 39, pp. 426-447, (1982)
[10]  
Brantley R.K., Ontogeny of inter- and intrasexual dimorphism in a vocalizing fish: Behavioral, morphological, and endocrine correlates, (1992)