Lorena S. Vieira , Diego F.B. Vaz , Andre L. Netto-Ferreira
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引用次数: 0
Abstract
The batracoidid Plainfin Midshipmen Porichthys notatus Girard has been extensively studied due to the sound production abilities and specializations of its swim bladder. The present study describes three-dimensional variations of the morphology of the swim bladder and sonic muscles of P. notatus during its post-hatch larval development, with the use of three-dimensional computed tomography. This study also includes descriptions of the relative position of the swim bladder to other visceral organs. The swim bladder, digestive tract, and liver were already present in the smallest examined specimens (5.9 mm; newly hatched larvae) along with the yolk sac. In the smallest specimens, the digestive tract is straight, but from 7.1 mm TL, the digestive tract forms the first intestinal loops, and at 25.5 mm TL, a second intestinal loop. In smallest specimens, the swim bladder is oval, but at 7.1 mm TL, the anterior margin starts invaginating, forming a pair of anterior lobes. The first appearance of the intrinsic sonic muscles in swim bladder occurs at 13.1 mm TL. Additionally, we provide comparisons between the shape of the swim bladder of P. notatus and other species. The shape of the swim bladder of P. notatus and other members of Porichthyinae have an ovoid posterior region with two anterior lobes and differs from the cordiform or semiconected/bilobed the swim bladders observed in the other Batrachoididae.
由于其鱼鳔的发声能力和特殊性,斑尾鱼已被广泛研究。本研究利用三维计算机断层扫描技术描述了斑点蛙在孵化后幼虫发育过程中膀胱和声波肌形态的三维变化。这项研究还包括对鱼鳔与其他内脏器官的相对位置的描述。膀胱、消化道和肝脏已经存在于最小的检查标本(5.9毫米;新孵化的幼虫)以及卵黄囊中。在最小的标本中,消化道是直的,但从7.1毫米的TL开始,消化道形成第一个肠环,在25.5毫米的TL形成第二个肠环。在最小的标本中,鱼鳔是椭圆形的,但在7.1毫米的TL处,前边缘开始内陷,形成一对前叶。鱼鳔中固有声波肌的首次出现发生在13.1 mm TL处。此外,我们还对P.nottus和其他物种的鱼鳔形状进行了比较。P.nottus和Porchhyinae的其他成员的鱼鳔的形状有一个带两个前叶的卵球形后部区域,不同于在另一蝙蝠科中观察到的心形或半封闭/双叶的鱼鳔。
期刊介绍:
Zoology is a journal devoted to experimental and comparative animal science. It presents a common forum for all scientists who take an explicitly organism oriented and integrative approach to the study of animal form, function, development and evolution.
The journal invites papers that take a comparative or experimental approach to behavior and neurobiology, functional morphology, evolution and development, ecological physiology, and cell biology. Due to the increasing realization that animals exist only within a partnership with symbionts, Zoology encourages submissions of papers focused on the analysis of holobionts or metaorganisms as associations of the macroscopic host in synergistic interdependence with numerous microbial and eukaryotic species.
The editors and the editorial board are committed to presenting science at its best. The editorial team is regularly adjusting editorial practice to the ever changing field of animal biology.