Ladich F, Bass A H
Institute of Zoology, University of Vienna, Wien, Austria.
Brain Behav Evol. 1998;51(6):315-30. doi: 10.1159/000006545.
Among teleost fishes, representatives of several distantly related groups have sound-producing (sonic/vocal) muscles associated with the swimbladder or pectoral girdle/fin. Here, the diversity of vocal organs and central motor pathways in four families of catfish, order Siluriformes, is compared to that in families from two distantly related orders, the Scorpaeniformes and Batrachoidiformes. Several catfish families have two sonic mechanisms--a swimbladder vibration established by 'drumming muscles' that differ in origin and insertion between families, and a pectoral spine stridulatory apparatus. In ariids, mochokids and doradids, sonic swimbladder muscles originate at various cranial or postcranial elements and insert onto an 'elastic spring' that vibrates the swimbladder, while in pimelodids the muscles insert ventrally at the swimbladder. Sonic motoneurons are located along the midline, ventral to the fourth ventricle/central canal in doradids and mochokids but lateral to the medial longitudinal fasciculus in ariids; pimelodids have motoneurons in both locations. The axonal trajectory for the lateral motoneurons in pimelodids and ariids implies that they are a migrated, midline population of sonic motoneurons. Pectoral spine-associated motoneurons are located in the ventral motor column. Unlike catfishes, a diversity of sonic mechanisms in Scorpaeniformes is not associated with different positions for sonic motoneurons. Cottids (sculpin) lack a swimbladder but have sonic muscles that originate at the occipital cranium and insert at the pectoral girdle; sonic motoneurons are located within the ventral motor column. Some triglids have intrinsic swimbladder muscles, although ontogenetic data indicate a transient association with the pectoral girdle; sonic motoneurons are in the same location as in cottids. Among Batrachoidiformes, all known representatives have intrinsic swimbladder muscles that are never associated with the pectoral girdle and are innervated by midline sonic motoneurons. The results suggest two patterns of organization for sound-producing systems in teleost fishes: pectoral fin/girdle-associated muscles are innervated by sonic motoneurons positioned within the ventral motor column, adjacent to the ventral fasciculus; non-pectoral associated muscles are innervated by sonic motoneurons located on or close to the midline, adjacent to the medial longitudinal fasciculus.
在硬骨鱼类中,几个远缘类群的代表都有与鳔或胸带/胸鳍相关的发声(声波/发声)肌肉。在此,将鲶形目四个科的发声器官和中枢运动通路的多样性与两个远缘目的科,即鲉形目和蟾鱼目的科进行了比较。几个鲶鱼科有两种发声机制——一种是由“击鼓肌肉”建立的鳔振动,不同科的击鼓肌肉在起点和止点上有所不同,另一种是胸鳍棘摩擦发声器官。在海鲶科、蝌蚪鲶科和陶乐鲶科中,发声鳔肌起源于各种头前部或头后部结构,并插入到一个使鳔振动的“弹性弹簧”上,而在油鲶科中,这些肌肉腹侧插入鳔。发声运动神经元位于中线沿线,在陶乐鲶科和蝌蚪鲶科中位于第四脑室/中央管的腹侧,但在海鲶科中位于内侧纵束的外侧;油鲶科在这两个位置都有运动神经元。油鲶科和海鲶科外侧运动神经元的轴突轨迹表明它们是迁移而来的中线发声运动神经元群体。与胸鳍棘相关的运动神经元位于腹侧运动柱中。与鲶鱼不同,鲉形目多样的发声机制与发声运动神经元的不同位置无关。杜父鱼科(杜父鱼)没有鳔,但有起源于枕骨并插入胸带的发声肌肉;发声运动神经元位于腹侧运动柱内。一些鲂鮄科有内在的鳔肌,尽管个体发育数据表明其与胸带存在短暂关联;发声运动神经元与杜父鱼科的位置相同。在蟾鱼目中,所有已知代表都有从不与胸带相关联且由中线发声运动神经元支配的内在鳔肌。结果表明硬骨鱼类发声系统有两种组织模式:与胸鳍/胸带相关的肌肉由位于腹侧运动柱内、与腹侧束相邻的发声运动神经元支配;与胸鳍无关的肌肉由位于中线或靠近中线、与内侧纵束相邻的发声运动神经元支配。