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Chapter 12 – Relationships of Lower Euteleostean Fishes

TLDR
In the first Interrelationships of Fishes lower euteleosts were omitted and Fink (1984a) summarized the history of protacanthopterygians as "erosion" and "attrition, most notably at the hands of Rosen (1973)"
Abstract
In the first Interrelationships of Fishes lower euteleosts, or "protacanthopterygians" as they were then called, were omitted, with only a comment in the Preface citing Weitzman (1967, on osmeroids and stomiatoids), McDowall (1969, on osmeroids and galaxioids), Rosen and Greenwood (1970, on gonorynchiforms and ostariophysans), Greenwood and Rosen (1971, on argentinoids and alepocephaloids), and Nelson (1970b, on salangids and argentinids; 1972, on esocoids and galaxioids). Ten years later, in Ontogeny and Systematics of Fishes, Fink (1984a) summarized the history of protacanthopterygians as "erosion" and "attrition, most notably at the hands of Rosen (1973)" [in the first Interrelationships of Fishes]. Fink then saw the problems as these: (1) What are the relationships of the Esocoidei? (2) What are the relationships of the Ostariophysi? Do these fishes lie above or below the Esocoidei? (3) What is the pattern of relationships among the traditional "salmoniform" taxa, exclusive of Esocoidei and Ostariophysi? (4) What are the relationships of and within the Argentinoidei (sensu Greenwood and Rosen, 1971, i.e., argentinoids plus alepocephaloids)? (5) What are the relationships of and within the Osmeroidei? (6) What are the relationships of and within Salmonidae? (7) Where does Lepidogalaxias belong? (8) What are the relationships within stomiiform fishes? (9) What of the Myctophoidei, as recognized by Greenwood et al. (1966, i.e., Aulopiformes and Myctophiformes in current terminology)? In that agenda, items (8) and (9) are treated elsewhere in this volume and do not concern us, but items (1) through (7) do. Some classifications and/or cladograms of lower euteleosts, dating back to the first application of cladistic method, are summarized in Fig. 1. As is obvious from incongruence between all the patterns in Fig. 1, there has been protracted argument on how lower euteleostean groups are interrelated, how they are related to neoteleosts (stomiiforms and eurypterygians, Johnson, 1992), and what group is basal to other euteleosts. The most substantial treatment of these problems is in Begle's (1991,1992) cladistic analyses of Osmeroidei (1991) and Argentinoidei (1992) (Fig. 1G). Begle's two papers resulted in the cladogram in Fig. 2, in which the terminals are the genera or higher taxa sampled in his matrix. His classification (Begle, 1991, fig.l; 1992, table 2) to family level, without ranks above the superfamily and sequenced according to the conventions of Wiley (1981), was as follows:

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Citations
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Mitogenomic Exploration of Higher Teleostean Phylogenies: A Case Study for Moderate-Scale Evolutionary Genomics with 38 Newly Determined Complete Mitochondrial DNA Sequences

TL;DR: It is concluded that purposeful higher-density taxonomic sampling, subsequent sequencing efforts, and phylogenetic analyses of their mitogenomes may be decisive in resolving persistent controversies over higher-level relationships of teleosts, the most diversified group of all vertebrates, comprising over 23,500 extant species.
Journal ArticleDOI

Use of Mitogenomic Information in Teleostean Molecular Phylogenetics: A Tree-Based Exploration under the Maximum-Parsimony Optimality Criterion

TL;DR: It is concluded that judicious choice of mitochondrial genes and appropriate data weighting, in conjunction with purposeful taxonomic sampling, are prerequisites for resolving higher-level relationships in teleosts under the maximum-parsimony optimality criterion.
Journal ArticleDOI

Crying wolf, crying foul, or crying shame: alien salmonids and a biodiversity crisis in the southern cool-temperate galaxioid fishes?

TL;DR: The galaxioid fishes are the dominant, most speciose group of freshwater fishes (with >50 species) in the lands of the cool southern hemisphere, with representatives in western and eastern Australia, Tasmania, New Caledonia, Lord Howe Island, New Zealand, the Chatham, Auckland and Campbell Islands, Patagonian South America.
Journal ArticleDOI

The evolution of diadromy in fishes (revisited) and its place in phylogenetic analysis

TL;DR: Examination of fishes shows wide variability of diadromous life histories within closely related families and genera, within species, and there is even ontogenetic variation in patterns of behaviour by individual fish, which suggests diadromy is a behavioural character of dubious worth in determining phylogenetic relationships.
References
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Journal ArticleDOI

Interrelationships of the ostariophysan fishes (Teleostei)

TL;DR: The extent of sympatry, together with the widespread distribution of ostariophysan lineages, suggests that the group is older than previously supposed, and hypotheses of relationships implies that many of the extent characiform lineages evolved before the separation of Africa and South America.