Geremías Sánchez-Pinedo, N. Díaz-Viloria, J. L. Ortíz-Galindo, Nelson Ferreira-Fontoura, R. Pérez-Enríquez, L. Sánchez‐Velasco, J. De La Cruz‐Agüero
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引用次数: 0
摘要
摘要:在Sciaenidae科中,Micropogonias属由墨西哥太平洋沿岸的三个已知物种组成:Micropogonias altipinnis, M. ectenes和M. megalops。这些物种表现出重叠的诊断特征,这使得物种鉴定变得困难。本研究将太平洋Micropogonias物种之间的形态差异(分生、身体形态和耳石)与DNA序列(mtDNA的CO1和16S部分以及nDNA的28S部分)联系起来。分生分析表明,三种鱼在鳐数、鳃耙数和背鳍最长棘长度上存在纬度差异,形态计量特征(体和耳石)判别分析显示三种形态实体(p < 2%)。遗传结果表明,这三个物种是一个物种,分型和形态的差异可能是表型可塑性或早期物种形成的结果。在这个意义上,M. ectenes和M. megalops被认为是M. altipinnis的初级近义词。
Proposed synonymy for Micropogonias altipinnis (Günther 1864), Micropogonias ectenes (Jordan & Gilbert 1882), and Micropogonias megalops (Gilbert 1890)
Abstract Within the Sciaenidae family, the genus Micropogonias is composed of three recognized species along the Pacific coast of Mexico: Micropogonias altipinnis, M. ectenes, and M. megalops. These species exhibit overlapping diagnostic characters, which make species identification difficult. This study ties morphological differences (meristic, morphometry of body, and otolith) with DNA sequences (CO1 and 16S fractions of mtDNA and 28S of nDNA) among Micropogonias species in the Pacific. Meristic analysis showed a latitudinal variation among the three species in the number of rays, the number of gill rakers, and length of the longest spine of the dorsal fin. Discriminant analysis of morphometric characters (body and otolith) showed three morphological entities (p < 0.001). However, the mean genetic divergences among the three species with partial sequences of mtDNA (CO1 and 16S), and nuclear (28S) were lower than those reported at the interspecific level (>2%). Genetic results suggest that the three species are one species and that the differences in meristics and morphometry could be the result of phenotypic plasticity or incipient speciation. In this sense, M. ectenes and M. megalops are proposed as junior synonyms of M. altipinnis.
期刊介绍:
Mitochondrial DNA Part A publishes original high-quality manuscripts on physical, chemical, and biochemical aspects of mtDNA and proteins involved in mtDNA metabolism, and/or interactions. Manuscripts on cytosolic and extracellular mtDNA, and on dysfunction caused by alterations in mtDNA integrity as well as methodological papers detailing novel approaches for mtDNA manipulation in vitro and in vivo are welcome. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, phylogenetics and human evolution that use mitochondrial DNA as a source of evidence for studies will be considered for publication. The Journal also considers manuscripts that examine population genetic and systematic theory that specifically address the use of mitochondrial DNA sequences, as well as papers that discuss the utility of mitochondrial DNA information in medical studies and in human evolutionary biology.