Gibbs Melissa Ann
Department of Biology, Stetson University, DeLand, Fla 32723, USA.
Brain Behav Evol. 2004;64(3):163-81. doi: 10.1159/000079745.
The lateral line system is composed of both mechanoreceptors, which exhibit little variation in structure between taxonomic groups, and electroreceptors, which exhibit considerably more variation. Cathodally sensitive ampullary electroreceptors are the primitive condition and are found in agnathans, chondrichthyans, and most osteichthyans. Aquatic amphibians also have ampullary electroreceptors for at least part of their life cycle. The more recently evolved anodally sensitive ampullary electroreceptors and tuberous electroreceptors are only found in four groups of teleost fishes. The basic ontogenetic unit of lateral line development is the dorsolateral placode. Primitively, there are six pairs of placodes, which pass through sequential stages of development into lateral line receptors. There is no question about the origin of primitive mechanoreceptors or electroreceptors, however, we do not have a good understanding of the origin of teleost mechanoreceptors and their ampullary or tuberous electroreceptors; do they come exclusively from dorsolateral placodes or from neural crest or even general ectoderm? A second intriguing lateral line question is how certain teleost fish groups evolved tuberous electroreceptors. Electroreception appears to have re-evolved at least twice in teleosts after being lost during the neopterygian radiation. It has been suggested that the development of tuberous electroreceptors might be due to changes in placodal patterning or a change in the general ectoderm that placodes arise from. Unfortunately, our understanding of lateral line origins in fishes is very sketchy, and, if we are to answer such an evolutionary question, we first need more complete information about lateral line development in a variety of fishes, which can then be combined with gene expression data to better interpret lateral line receptor development.
侧线系统由机械感受器和电感受器组成,机械感受器在分类群之间结构变化很小,而电感受器的结构变化则大得多。阴极敏感的壶腹电感受器是原始状态,见于无颌类、软骨鱼类和大多数硬骨鱼类。水生两栖动物在其生命周期的至少一部分时间里也有壶腹电感受器。最近进化出的阳极敏感壶腹电感受器和结节状电感受器仅在四类硬骨鱼类中发现。侧线发育的基本个体发生单位是背外侧基板。原始情况下,有六对基板,它们经过连续的发育阶段成为侧线感受器。原始机械感受器或电感受器的起源是毫无疑问的,然而,我们对硬骨鱼机械感受器及其壶腹或结节状电感受器的起源了解并不充分;它们是完全来自背外侧基板,还是来自神经嵴甚至是一般外胚层呢?另一个有趣的侧线问题是某些硬骨鱼群是如何进化出结节状电感受器的。电感受在新鳍鱼辐射期间丧失后,似乎在硬骨鱼中至少重新进化了两次。有人提出,结节状电感受器的发育可能是由于基板模式的变化或基板所起源的一般外胚层的变化。不幸的是,我们对鱼类侧线起源的了解非常粗略,如果我们要回答这样一个进化问题,我们首先需要关于各种鱼类侧线发育的更完整信息,然后将其与基因表达数据结合起来,以更好地解释侧线感受器的发育。