Malmberg G
Department of Zoology, Stockholm University, Sweden.
Int J Parasitol. 1998 Oct;28(10):1625-35. doi: 10.1016/s0020-7519(98)00058-7.
On the basis of six main types of protonephridial systems in the genus Gyrodactylus and results from further studies of the protonephridial systems in other gyrodactylid genera and other monogenean families, evolutionary lines within the Gyrodactylidae and the origin of the genera Ooegyrodactylus, Swingleus, Gyrdicotylus and Polyclithrum are discussed. An excretory bladder (on both sides of the body) with separate openings for the main canals of the anterior and the posterior systems, a median junction between the two anterior systems and likewise a junction between the two posterior systems, many flame bulbs and an absence of lateral flames in the main canals were found to be primitive monogenean characters. A system similar to that in the acanthocotylid larva but with secondarily evolved lateral flames in the posterior systems may have given rise to a first protogyrodactylid system, in turn giving rise to the system of Macrogyrodactylus. In a second protogyrodactylid line, the main canal of the anterior system (on both sides of the body) was connected to that of the posterior system and lateral flames were developed also in the anterior system. From this system all other described gyrodactylid systems may arise: one main line gave rise to the system of the G. (Gyrodactylus) and another to a system of G. (Mesonephrothus) type. The systems of Swingleus and Gyrdicotylus are of the latter type. Through loss of all lateral flames, the system of G. (Metanephrotus) may have evolved. Isancistrum has a system of the G. (Metanephrotus) type. From this type of system, those of Polyclithrum, G. (Neonephrotus), G. (Paranephrotus) and G. (Limnonephrotus) can be derived. The fact that the system of Ooegyrodactylus is more closely related to that of G. (Gyrodactylus) than to that of Macrogyrodactylus prompts discussion regarding the evolution of the viviparity of the family Gyrodactylidae. According to the evolutionary system presented, primitive gyrodactylids parasitise primitive fish species and the most advanced gyrodactylids parasitise the most advanced fish species. However, Anguillidae and Clupeidae may have been secondarily infected by members of G. (Metanephrotus) and G. (Neonephrotus) respectively, and Cyprinidae, Salmonidae and Esocidae may similarly have been secondarily infected by members of G. (Limnonephrotus). Isancistrum may have infected squids (Loligidae) at a medium level in the evolution within the Gyrodactylidae, while progenitors of Gyrdicotylus may have been adapted to clawed toads (Xenopidae) earlier in evolution.
基于三代虫属原肾管系统的六种主要类型,以及对其他三代虫科属和其他单殖吸虫科原肾管系统的进一步研究结果,本文讨论了三代虫科内部的进化谱系以及卵形三代虫属、斯温格三代虫属、回旋三代虫属和多枝三代虫属的起源。排泄膀胱(位于身体两侧),前后系统的主管道有独立开口,两个前系统之间有一个中间连接,两个后系统之间同样有一个连接,许多焰细胞,主管道中没有侧焰,这些被认为是原始单殖吸虫的特征。一种与棘杯科幼虫相似但后系统中侧焰次生进化的系统可能产生了第一个原三代虫系统,进而产生了巨三代虫属的系统。在第二条原三代虫谱系中,前系统的主管道(位于身体两侧)与后系统的主管道相连,前系统中也发育出了侧焰。所有其他已描述的三代虫系统可能都源于这个系统:一条主线产生了三代虫属(三代虫)的系统,另一条产生了中肾三代虫属类型的系统。斯温格三代虫属和回旋三代虫属的系统属于后一种类型。通过失去所有侧焰,后肾三代虫属的系统可能已经进化。伊桑吸虫属有一个后肾三代虫属类型的系统。从这种系统类型可以衍生出多枝三代虫属、新肾三代虫属、副肾三代虫属和湖肾三代虫属的系统。卵形三代虫属的系统与三代虫属(三代虫)的系统比与巨三代虫属的系统关系更密切,这一事实引发了关于三代虫科胎生进化的讨论。根据所提出的进化系统,原始三代虫寄生于原始鱼类物种,最先进的三代虫寄生于最先进的鱼类物种。然而,鳗鲡科和鲱科可能分别被后肾三代虫属和新肾三代虫属的成员次生感染,鲤科、鲑科和狗鱼科可能同样被湖肾三代虫属的成员次生感染。在三代虫科的进化过程中,伊桑吸虫属可能在中等水平上感染了鱿鱼(枪乌贼科),而回旋三代虫属的祖先可能在进化早期就适应了爪蟾(负子蟾科)。