RESUMEN

Nine new species of Phenacogaster Eigenmann, 1907 are described: Phenacogaster capitulatus sp. nov. from the Neshuya River system, Ucayali River basin; Phenacogaster maculoblongus sp. nov. from the upper Cuyuni River, and tributaries of the lower Orinoco River; Phenacogaster napoatilis sp. nov. from the Napo River system, upper Amazon River basin; Phenacogaster ojitatus sp. nov. from the Xingu River system; Phenacogaster prolatus sp. nov. from the Orinoco River, canal Casiquiare and upper and middle Negro River; Phenacogaster retropinnus sp. nov. from the Negro, Madeira and Xingu river systems; Phenacogaster simulatus sp. nov. from the Potaro River, Essequibo drainage; Phenacogaster wayampi sp. nov. from the Oiapoque River, and Phenacogaster wayana sp. nov. from the Corantijn (Suriname), Maroni, Mana, Sinnamary and Approuague rivers (French Guiana). The geographic distribution of P. megalostictus, previously recorded for the Negro River, Amazon River system, is restricted to the Essequibo River system, Guiana. The distribution of P. carteri, previously known only from the type-locality (Cuyuni River, Guyana), is extended to the lower Orinoco River. The reduction of the latero-sensory canal, mentioned in the literature as an autapomorphy for P. tegatus was observed in three additional species of Phenacogaster. The posterior humeral spot, found only in P. tegatus, is herein considered autapomorphic for the species. Diagnoses are given for previously described species based on the analysis of type material and additional specimens, and a key to the species of the genus is provided.

RESUMEN

Nine new species of Phenacogaster Eigenmann, 1907 are described: Phenacogaster capitulatus sp. nov. from the Neshuya River system, Ucayali River basin; Phenacogaster maculoblongus sp. nov. from the upper Cuyuni River, and tributaries of the lower Orinoco River; Phenacogaster napoatilis sp. nov. from the Napo River system, upper Amazon River basin; Phenacogaster ojitatus sp. nov. from the Xingu River system; Phenacogaster prolatus sp. nov. from the Orinoco River, canal Casiquiare and upper and middle Negro River; Phenacogaster retropinnus sp. nov. from the Negro, Madeira and Xingu river systems; Phenacogaster simulatus sp. nov. from the Potaro River, Essequibo drainage; Phenacogaster wayampi sp. nov. from the Oiapoque River, and Phenacogaster wayana sp. nov. from the Corantijn (Suriname), Maroni, Mana, Sinnamary and Approuague rivers (French Guiana). The geographic distribution of P. megalostictus, previously recorded for the Negro River, Amazon River system, is restricted to the Essequibo River system, Guiana. The distribution of P. carteri, previously known only from the type-locality (Cuyuni River, Guyana), is extended to the lower Orinoco River. The reduction of the latero-sensory canal, mentioned in the literature as an autapomorphy for P. tegatus was observed in three additional species of Phenacogaster. The posterior humeral spot, found only in P. tegatus, is herein considered autapomorphic for the species. Diagnoses are given for previously described species based on the analysis of type material and additional specimens, and a key to the species of the genus is provided.

RESUMEN

Nine new species of Phenacogaster Eigenmann, 1907 are described: Phenacogaster capitulatus sp. nov. from the Neshuya River system, Ucayali River basin; Phenacogaster maculoblongus sp. nov. from the upper Cuyuni River, and tributaries of the lower Orinoco River; Phenacogaster napoatilis sp. nov. from the Napo River system, upper Amazon River basin; Phenacogaster ojitatus sp. nov. from the Xingu River system; Phenacogaster prolatus sp. nov. from the Orinoco River, canal Casiquiare and upper and middle Negro River; Phenacogaster retropinnus sp. nov. from the Negro, Madeira and Xingu river systems; Phenacogaster simulatus sp. nov. from the Potaro River, Essequibo drainage; Phenacogaster wayampi sp. nov. from the Oiapoque River, and Phenacogaster wayana sp. nov. from the Corantijn (Suriname), Maroni, Mana, Sinnamary and Approuague rivers (French Guiana). The geographic distribution of P. megalostictus, previously recorded for the Negro River, Amazon River system, is restricted to the Essequibo River system, Guiana. The distribution of P. carteri, previously known only from the type-locality (Cuyuni River, Guyana), is extended to the lower Orinoco River. The reduction of the latero-sensory canal, mentioned in the literature as an autapomorphy for P. tegatus was observed in three additional species of Phenacogaster. The posterior humeral spot, found only in P. tegatus, is herein considered autapomorphic for the species. Diagnoses are given for previously described species based on the analysis of type material and additional specimens, and a key to the species of the genus is provided.

RESUMEN

The analysis of the material obtained in the rescue of archaeological sites in the area surrounding the Hydroelectric Plant of Machadinho, Rio Grande do Sul, revealed that a considerable amount of bones and fish scales incorporated in the alimentary remains. Using an osteological collection as reference, we identified remains of Salminus brasiliensis (Cuvier, 1816) (Characidae), Brycon orbignyanus (Valenciennes, 1849) (Characidae), Pogonopoma obscurum Quevedo & Reis, 2002 (Loricariidae), Hemiancistrus fuliginosus Cardoso & Malabarba, 1999, Prochilodus lineatus (Valenciennes, 1836) (Prochilodontidae), Schizodon sp. (Anostomidae), Leporinus sp. (Anostomidae), Hoplias sp. (Erythrinidae), Hypostomus sp. (Loricariidae) and Crenicichla sp. (Cichlidae). Based on specimens from fish collections, regressions were obtained comparing the size of the pre-maxillary bone in Crenicichla spp. and the length of the pectoral fin spine of Hemiancistrus fuliginosus, Pogonopoma obscurum and Hypostomus spp, with the standard length and weight of corresponding specimens. The estimated size and weight of the specimens obtained from fish remains in the archaeological sites varied between 79.7-153.9 mm and 13.5-33.9 g for Hemiancistrus fuliginosus, 158.2-151.0 mm and 179.5-194.3 g for Pogonopoma obscurum, 117.1-166.2 mm and 86.6-93.1 g for Crenicichla spp., and 62.2-397.2 mm and 34-20.3 g for Hypostomus spp. Therefore using these estimates of standard lengths and weights it was possible to formulate a hypotheses on the fishing technology used by the inhabitants of these sites.

RESUMEN

The analysis of the material obtained in the rescue of archaeological sites in the area surrounding the Hydroelectric Plant of Machadinho, Rio Grande do Sul, revealed that a considerable amount of bones and fish scales incorporated in the alimentary remains. Using an osteological collection as reference, we identified remains of Salminus brasiliensis (Cuvier, 1816) (Characidae), Brycon orbignyanus (Valenciennes, 1849) (Characidae), Pogonopoma obscurum Quevedo & Reis, 2002 (Loricariidae), Hemiancistrus fuliginosus Cardoso & Malabarba, 1999, Prochilodus lineatus (Valenciennes, 1836) (Prochilodontidae), Schizodon sp. (Anostomidae), Leporinus sp. (Anostomidae), Hoplias sp. (Erythrinidae), Hypostomus sp. (Loricariidae) and Crenicichla sp. (Cichlidae). Based on specimens from fish collections, regressions were obtained comparing the size of the pre-maxillary bone in Crenicichla spp. and the length of the pectoral fin spine of Hemiancistrus fuliginosus, Pogonopoma obscurum and Hypostomus spp, with the standard length and weight of corresponding specimens. The estimated size and weight of the specimens obtained from fish remains in the archaeological sites varied between 79.7-153.9 mm and 13.5-33.9 g for Hemiancistrus fuliginosus, 158.2-151.0 mm and 179.5-194.3 g for Pogonopoma obscurum, 117.1-166.2 mm and 86.6-93.1 g for Crenicichla spp., and 62.2-397.2 mm and 34-20.3 g for Hypostomus spp. Therefore using these estimates of standard lengths and weights it was possible to formulate a hypotheses on the fishing technology used by the inhabitants of these sites.

RESUMEN

The analysis of the material obtained in the rescue of archaeological sites in the area surrounding the Hydroelectric Plant of Machadinho, Rio Grande do Sul, revealed that a considerable amount of bones and fish scales incorporated in the alimentary remains. Using an osteological collection as reference, we identified remains of Salminus brasiliensis (Cuvier, 1816) (Characidae), Brycon orbignyanus (Valenciennes, 1849) (Characidae), Pogonopoma obscurum Quevedo & Reis, 2002 (Loricariidae), Hemiancistrus fuliginosus Cardoso & Malabarba, 1999, Prochilodus lineatus (Valenciennes, 1836) (Prochilodontidae), Schizodon sp. (Anostomidae), Leporinus sp. (Anostomidae), Hoplias sp. (Erythrinidae), Hypostomus sp. (Loricariidae) and Crenicichla sp. (Cichlidae). Based on specimens from fish collections, regressions were obtained comparing the size of the pre-maxillary bone in Crenicichla spp. and the length of the pectoral fin spine of Hemiancistrus fuliginosus, Pogonopoma obscurum and Hypostomus spp, with the standard length and weight of corresponding specimens. The estimated size and weight of the specimens obtained from fish remains in the archaeological sites varied between 79.7-153.9 mm and 13.5-33.9 g for Hemiancistrus fuliginosus, 158.2-151.0 mm and 179.5-194.3 g for Pogonopoma obscurum, 117.1-166.2 mm and 86.6-93.1 g for Crenicichla spp., and 62.2-397.2 mm and 34-20.3 g for Hypostomus spp. Therefore using these estimates of standard lengths and weights it was possible to formulate a hypotheses on the fishing technology used by the inhabitants of these sites.

RESUMEN

The analysis of the material obtained in the rescue of archaeological sites in the area surrounding the Hydroelectric Plant of Machadinho, Rio Grande do Sul, revealed that a considerable amount of bones and fish scales incorporated in the alimentary remains. Using an osteological collection as reference, we identified remains of Salminus brasiliensis (Cuvier, 1816) (Characidae), Brycon orbignyanus (Valenciennes, 1849) (Characidae), Pogonopoma obscurum Quevedo & Reis, 2002 (Loricariidae), Hemiancistrus fuliginosus Cardoso & Malabarba, 1999, Prochilodus lineatus (Valenciennes, 1836) (Prochilodontidae), Schizodon sp. (Anostomidae), Leporinus sp. (Anostomidae), Hoplias sp. (Erythrinidae), Hypostomus sp. (Loricariidae) and Crenicichla sp. (Cichlidae). Based on specimens from fish collections, regressions were obtained comparing the size of the pre-maxillary bone in Crenicichla spp. and the length of the pectoral fin spine of Hemiancistrus fuliginosus, Pogonopoma obscurum and Hypostomus spp, with the standard length and weight of corresponding specimens. The estimated size and weight of the specimens obtained from fish remains in the archaeological sites varied between 79.7-153.9 mm and 13.5-33.9 g for Hemiancistrus fuliginosus, 158.2-151.0 mm and 179.5-194.3 g for Pogonopoma obscurum, 117.1-166.2 mm and 86.6-93.1 g for Crenicichla spp., and 62.2-397.2 mm and 34-20.3 g for Hypostomus spp. Therefore using these estimates of standard lengths and weights it was possible to formulate a hypotheses on the fishing technology used by the inhabitants of these sites.

RESUMEN

The analysis of the material obtained in the rescue of archaeological sites in the area surrounding the Hydroelectric Plant of Machadinho, Rio Grande do Sul, revealed that a considerable amount of bones and fish scales incorporated in the alimentary remains. Using an osteological collection as reference, we identified remains of Salminus brasiliensis (Cuvier, 1816) (Characidae), Brycon orbignyanus (Valenciennes, 1849) (Characidae), Pogonopoma obscurum Quevedo & Reis, 2002 (Loricariidae), Hemiancistrus fuliginosus Cardoso & Malabarba, 1999, Prochilodus lineatus (Valenciennes, 1836) (Prochilodontidae), Schizodon sp. (Anostomidae), Leporinus sp. (Anostomidae), Hoplias sp. (Erythrinidae), Hypostomus sp. (Loricariidae) and Crenicichla sp. (Cichlidae). Based on specimens from fish collections, regressions were obtained comparing the size of the pre-maxillary bone in Crenicichla spp. and the length of the pectoral fin spine of Hemiancistrus fuliginosus, Pogonopoma obscurum and Hypostomus spp, with the standard length and weight of corresponding specimens. The estimated size and weight of the specimens obtained from fish remains in the archaeological sites varied between 79.7-153.9 mm and 13.5-33.9 g for Hemiancistrus fuliginosus, 158.2-151.0 mm and 179.5-194.3 g for Pogonopoma obscurum, 117.1-166.2 mm and 86.6-93.1 g for Crenicichla spp., and 62.2-397.2 mm and 34-20.3 g for Hypostomus spp. Therefore using these estimates of standard lengths and weights it was possible to formulate a hypotheses on the fishing technology used by the inhabitants of these sites.

RESUMEN

Spermiogenesis in the curimatid species, Steindachnerina insculpta, Cyphocharax gillii, C. modestus, C. spilotus, and Potamorhina altamazonica, is characterized by lateral development of the flagellum, nuclear rotation, eccentric nuclear fossa formation, and chromatin compacted into thick fibers. These spermatozoa exhibit a spherical head containing a nucleus with the chromatin highly condensed into thick fibers with small electron-lucent areas, and no acrosome. The nuclear fossa is of the moderate type and eccentric and penetrated by the centriolar complex. The midpiece is small, has many elongate vesicles, and a short cytoplasmic channel. Mitochondria may be elongate, branched or C-shaped, and are separated from the initial segment of the axoneme by the cytoplasmic channel. The flagellum contains the classical axoneme structure (9+2) and has a membranous compartment in the initial region; it does not have lateral fins. Only small differences were observed among the analyzed species and genera of the Curimatidae. Spermiogenesis and spermatozoa in the Curimatidae have many of the characteristics found in almost all other characiform species. On the other hand, the presence of a membranous compartment in the initial region of curimatid flagella, a structure common in many Cypriniformes spermatozoa, is unknown in other characiforms. Spermiogenesis and the spermatozoa of the Characiformes are discussed.

A espermiogênese nas espécies Steindachnerina insculpta, Cyphocharax gillii, C. modestus, C. spilotus e Potamorhina altamazonica de Curimatidae é caracterizada pelo desenvolvimento lateral do flagelo, rotação do núcleo, formação excêntrica da fossa nuclear e cromatina compactada em fibras espessas. Estes espermatozóides exibem uma cabeça esférica contendo um núcleo com cromatina altamente condensada em fibras espessas com pequenas áreas eletronlúcidas, e sem acrossoma. A fossa nuclear é do tipo moderado e excêntrico, penetrada pelo complexo centriolar. A peça média é pequena, tem muitas vesículas alongadas e um curto canal citoplasmático. Mitocôndrias podem ser alongadas, ramificadas ou em forma de C, e são separadas do segmento inicial do axonema pelo canal citoplasmático. O flagelo contém a estrutura clássica do axonema (9+2) e tem um compartimento membranoso na região inicial; não possui expansões laterais ("fins"). Somente pequenas diferenças foram observadas entre as espécies e gêneros analisados de Curimatidae. A espermiogênese e os espermatozóides de Curimatidae têm muitas das características encontradas em quase todas as outras espécies de Characiformes. Por outro lado, a presença de um compartimento membranoso na região inicial do flagelo dos curimatídeos, uma estrutura comum nos espermatozóides de muitos cipriniformes, é desconhecida em outros characiformes. Discute-se sobre a espermiogênese e espermatozóides de Characiformes.

RESUMEN

Spermiogenesis in the curimatid species, Steindachnerina insculpta, Cyphocharax gillii, C. modestus, C. spilotus, and Potamorhina altamazonica, is characterized by lateral development of the flagellum, nuclear rotation, eccentric nuclear fossa formation, and chromatin compacted into thick fibers. These spermatozoa exhibit a spherical head containing a nucleus with the chromatin highly condensed into thick fibers with small electron-lucent areas, and no acrosome. The nuclear fossa is of the moderate type and eccentric and penetrated by the centriolar complex. The midpiece is small, has many elongate vesicles, and a short cytoplasmic channel. Mitochondria may be elongate, branched or C-shaped, and are separated from the initial segment of the axoneme by the cytoplasmic channel. The flagellum contains the classical axoneme structure (9+2) and has a membranous compartment in the initial region; it does not have lateral fins. Only small differences were observed among the analyzed species and genera of the Curimatidae. Spermiogenesis and spermatozoa in the Curimatidae have many of the characteristics found in almost all other characiform species. On the other hand, the presence of a membranous compartment in the initial region of curimatid flagella, a structure common in many Cypriniformes spermatozoa, is unknown in other characiforms. Spermiogenesis and the spermatozoa of the Characiformes are discussed.

A espermiogênese nas espécies Steindachnerina insculpta, Cyphocharax gillii, C. modestus, C. spilotus e Potamorhina altamazonica de Curimatidae é caracterizada pelo desenvolvimento lateral do flagelo, rotação do núcleo, formação excêntrica da fossa nuclear e cromatina compactada em fibras espessas. Estes espermatozóides exibem uma cabeça esférica contendo um núcleo com cromatina altamente condensada em fibras espessas com pequenas áreas eletronlúcidas, e sem acrossoma. A fossa nuclear é do tipo moderado e excêntrico, penetrada pelo complexo centriolar. A peça média é pequena, tem muitas vesículas alongadas e um curto canal citoplasmático. Mitocôndrias podem ser alongadas, ramificadas ou em forma de C, e são separadas do segmento inicial do axonema pelo canal citoplasmático. O flagelo contém a estrutura clássica do axonema (9+2) e tem um compartimento membranoso na região inicial; não possui expansões laterais ("fins"). Somente pequenas diferenças foram observadas entre as espécies e gêneros analisados de Curimatidae. A espermiogênese e os espermatozóides de Curimatidae têm muitas das características encontradas em quase todas as outras espécies de Characiformes. Por outro lado, a presença de um compartimento membranoso na região inicial do flagelo dos curimatídeos, uma estrutura comum nos espermatozóides de muitos cipriniformes, é desconhecida em outros characiformes. Discute-se sobre a espermiogênese e espermatozóides de Characiformes.