Characidae: Cheirodontinae: Compsurini)

Characidae: Cheirodontinae: Compsurini)

Neotropical Ichthyology, 9(2):299-312, 2011 Copyright © 2011 Sociedade Brasileira de Ictiologia Revision of the genus Macropsobrycon Eigenmann, 1915 (Characidae: Cheirodontinae: Compsurini) Fernando C. Jerep1 and Luiz R. Malabarba2 The cheirodontine genus Macropsobrycon is redefined and considered monotypic. The type species, M. uruguayanae, is redescribed based on samples from the entire known geographical distribution of the species. Sexually dimorphic characters of M. uruguayanae are further described and the relationships of the species with the remaining Compsurini are discussed. O gênero Macropsobrycon de Cheirodontinae é redefinido e considerado monotípico. A espécie-tipo, M. uruguayanae, é redescrita com base em amostras de toda a distribuição geográfica conhecida da espécie. Caracteres de dimorfismo sexual secundário de M. uruguayanae são descritos e as relações da espécie com outros Compsurini são discutidas. Key words: Neotropical, Sexual dimorphism, Systematics, Taxonomy. Introduction from Parecbasis by having fainter dentition and incomplete lateral line, from Aphyodite by having the caudal fin naked Historical review. Eigenmann (1915) described Macropsobrycon, and well developed pseudotympanum, and from Leptobrycon containing a single species, M. uruguayanae, in the subfamily by having the anal fin longer. Although consistent, Eigenmann’s Cheirodontinae. In the Eigenmann’s early concept of this description was incomplete in some aspects as the color pattern subfamily (now corresponding to Aphyocharacinae + of the dorsal and anal fins, and neither mentioned the complex Aphyoditeinae + Cheirodontinae + Paragoniatinae + some caudal-fin structures present on mature males. He still affirmed Tetragonopterinae characid genera sensu Mirande, 2010), the that scales were “apparently absent from caudal” causing Cheirodontinae diagnosis was presented in a topic uncertainty about the presence of them on the caudal fin. “Generalized type of the subfamily” in which he referred the Géry (1960), reviewing the morphological affinities of some conspicuous small body size, the single tooth series, and the Cheirodontinae, placed Macropsobrycon in an “intermediate teeth with “lateral notches” [cusps] to these characids. section” of the subfamily, jointly with 13 genera characterized Actually, the multicuspid teeth and the presence of one tooth by the presence of slender conical or tricuspid teeth, fourth series in the premaxilla and dentary have been the main infraorbital not developed, and presence of an adipose fin. In characters used in subsequent years to diagnose the this work, Géry split this “section” in three smaller groups, Cheirodontinae among characids (Eigenmann, 1915). In the situating Macropsobrycon with some other “degenetrate or end of the description of M. uruguayanae, notably Eigenmann specialized species” of the genera Parecbasis, Leptobrycon, considered that its conical teeth would “place it outside the Aphyodite, and Thrissobrycon Böhlke, based on the shared subfamily”, but also stated that its relationships [to presence of an elongated body, conical teeth reduced in number Cheirodontinae] are “unmistakable”. He further considered and size (at least on the maxilla), and a thicker and blade-like Macropsobrycon related to Parecbasis Eigenmann, maxilla. Géry still briefly distinguished Macropsobrycon from Aphyodite Eigenmann, Leptobrycon Eigenmann, and possibly these other genera by the presence of a superior mouth, to some Megalamphodus Eigenmann, all genera currently postorbitals (infraorbitals 4 and 5) not developed, fontanels removed from Cheirodontinae (Malabarba, 1998), differing short, lateral line incomplete, caudal naked, pseudotympanum 1Pontifícia Universidade Católica do Rio Grande do Sul, Laboratório de Sistemática de Vertebrados, Setor de Ictiologia, Museu de Ciências e Tecnologia. Av. Ipiranga 6681, 90619-900 Porto Alegre, RS, Brazil. [email protected] 2Universidade Federal do Rio Grande do Sul, Laboratório de Ictiologia, Departamento de Zoologia e Programa de Pós-Graduação em Biologia Animal, IB, UFRGS, Porto Alegre, RS, Brazil. [email protected] 299 300 Revision of the genus Macropsobrycon and some interhaemals (caudal-fin procurrent rays) present; Stevardiinae sensu Mirande, 2010), and Cheirodontinae, and described the shape of the Macropsobrycon premaxilla represented by M. uruguayanae. The same authors described and mesethmoid (dermethmoid in that paper) bones as identical briefly the spermatozoa ultrastructure of M. uruguayanae, to those of the representatives of the “tricuspid cheirodontines” and through new ultrastructural characters supported group, where the premaxilla is asymmetric with a high ascending Malabarba’s (1998) hypothesis of independent development process and low horizontal process, and the mesethmoid of insemination in the Glandulocaudinae and in the pointed. inseminating Cheirodontinae (now Compsurini). Later on, Géry (1965) also included Macropsobrycon in his phenetic the sperm ultrastructure of Macropsobrycon uruguayanae diagram with the representatives of the sub-tribe was described in detail by Oliveira et al. (2008), and its Aphyoditeini, suggesting that the genus could be the reproductive biology and gill gland development by Azevedo “junction” between the subgroup formed by Prodontocharax et al. (2010), making M. uruguayanae the best known Eigenmann & Pearson, Hyphessobrycon stigmatias Fowler, cheirodontine in terms of reproductive aspects to date. and Microschemobrycon Eigenmann; and the subgroups formed by Aphyodite, Brittanichthys, Leptobrycon, and Systematics and relationships. In a phylogenetic study, Parecbasis Géry. Later on, Géry (1972) proposed an updated Malabarba (1998) defined Cheirodontinae sensu stricto and phenetic diagram for the Aphyoditeini, where demonstrated cladistically that in the former systematic Macropsobrycon was grouped with Aphyodite representing arrangement of the subfamily the species were artificially a major group with Brittanichthys, Leptobrycon and grouped, and several genera and species were then removed Thrissobrycon. In this work, Géry also emphasized the from that taxon. Macropsobrycon uruguayanae, sharing the differences between Aphyocharax melanotus [sic] and main synapomorphies with the other members of the subfamily, Macropsobrycon uruguayanae, disagreeing with was kept in the more restricted group of the Cheirodontinae Eigenmann´s (1915) suggestion about a possible close as part of a new inseminating tribe, Compsurini. On the other relationship between these species, and proposed the new hand, M. xinguensis was considered species incertae sedis combination Microschemobrycon melanotus (Eigenmann). in Characidae, since it does not present all of the The genus remained monotypic up to Géry (1973) synapomorphies of the subfamily (Malabarba, 1998; Reis et description of Macropsobrycon xinguensis in a revisionary al., 2003). The genus Macropsobrycon was further diagnosed study of the “Aphyoditeina” species from the Amazon basin. by Malabarba (1998) based on four characters: (1) presence Géry (1973) quoted several differences between M. of a large space bearing hypertrophied tissue between the uruguayanae and M. xinguensis, like, for instance, the absence twelfth and thirteenth caudal-fin rays; (2) small and flexible of a humeral hiatus in his new species, as well as the presence spines present along the proximal portion of the lower lobe of partially scaled caudal-fin lobes, tricuspid teeth (vs. conical), principal caudal-fin rays; (3) jaw teeth elongated and conical dorsal-fin in front of mid-body, number of branched anal-fin or tricuspid [modified herein, see diagnosis of rays (17-18 vs. 19-22 in M. uruguayanae), number of perforated Macropsobrycon]; and (4) the dorsal-fin strongly black- lateral line scales (8 vs. 5-6 in M. uruguayanae), and a different pigmented along the mid-length of the second unbranched caudal color pattern. The placement of the new species in and first 5 branched rays [modified herein, see diagnosis of Macropsobrycon was considered by Géry a “conservative Macropsobrycon], and weakly pigmented along their distal solution”, taken “provisorily”, once both species have similar portion. characters like feeble teeth, toothless maxilla and incomplete Secondary sexual characters of M. uruguayanae have pored lateral line. Géry (1977) arranged the Cheirodontinae in been briefly discussed by Malabarba & Weitzman (1999, 2000) two major groups: the Cheirodontinae sensu stricto, and the and Malabarba et al. (2004) in comparison to Acinocheirodon “allied genera”. The group represented by the “allied genera” melanogramma Malabarba & Weitzman, Kolpotocheirodon was split in three tribes: Grundulini, Henochilini, and theloura Malabarba & Weitzman, and Kolpotocheirodon Probolodini. His former Aphyoditeina, including the figueiredoi Malabarba, Lima & Weitzman, respectively. Macropsobrycon species, was now treated as the “Aphyodite- Mirande (2009, 2010) proposed a hypothesis of group”, inside the tribe Grundulini together with the Grundulus- relationships among characid representatives and a new group and the Pristella-group. classification. Although the genus Macropsobrycon was kept in Cheirodontinae, none of its species were included in his Reprodutive biology. Little was known about the biology and analysis. Most recently, Javonillo et al. (2010) developed a reproductive characters of Macropsobrycon up to Burns et phylogenetic study within the Characidae based on molecular al. (1997) analysed histological sections of Macropsobrycon

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