Taxonomy of the catfish genus Pseudoplatystoma Bleeker  (Siluriformes: Pimelodidae) with recognition of eight species

Zootaxa ◽  
2007 ◽  
Vol 1512 (1) ◽  
pp. 1-38 ◽  
Author(s):  
URIEL ANGEL BUITRAGO–SUÁREZ ◽  
BROOKS M. BURR

The genus Pseudoplatystoma Bleeker consists of three species long recognized as: P. fasciatum (Linnaeus), P. tigrinum (Valenciennes), and P. corruscans (Spix & Agassiz), and five species recently recognized or described here: P. punctifer (Castelnau), P. reticulatum Eigenmann & Eigenmann, P. orinocoense n. sp., P. metaense n. sp., and P. magdaleniatum n. sp. The eight species form a monophyletic group with two clades that are supported by anatomical features (i.e., skeletal anatomy and myology). One clade (P. tigrinum and P. metaense) is restricted to the Orinoco and Amazon basins, and the other clade, comprised of the remaining six species, is found in the Guyanas, Orinoco, Amazon, and Paraná basins. The species are diagnosed on the basis of body shape, color pattern (e.g., bars, loops, and spots), skeletal anatomy, and vertebral numbers. Pseudoplatystoma punctifer and P. tigrinum) are sympatric in the Amazon Basin, P. metaense and P. orinocoense in the Orinoco Basin, and P. corruscans and P. reticulatum, are sympatric in the Paraná. Pseudoplatystoma magdaleniatum (Magdalena basin) and P. fasciatum (Guyanas) each occur as the only species of Pseudoplatystoma in their respective individual ranges. Pseudoplatystoma reticulatum may be sympatric with the two other species in the Amazon Basin, but we have no records of them being captured together in the mainstream or tributaries. All eight species are used as food in both commercial and subsistence fishing, and there is a moderate–sized ornamental fish market for the young and juveniles. A key to adults of the eight species is included.

2001 ◽  
Vol 133 (2) ◽  
pp. 155-164 ◽  
Author(s):  
Miguel Archangelsky ◽  
Marc A. Branham

AbstractThe last instar and pupa of Pyropyga nigricans (Say, 1823) are described, illustrated, and compared to those of Pyropyga modesta Green, 1961; these species differ in the color pattern of the pronotum and abdominal tergites, and the morphology of the maxilla and labium. Larvae of the genus Pyropyga Motschulsky, 1852 are compared to those of the genera Lamprohiza Motschulsky, 1853, Lucidota LeConte, 1833, and Phosphaenus Laporte, 1833 (all belonging to the tribe Photinini but to different subtribes); on the basis of general body shape and morphology of the head capsule, antennae, and mouthparts, larvae of the genus Pyropyga seem more closely related to those of the genus Lucidota than to those of the other two genera.


Zootaxa ◽  
2008 ◽  
Vol 1822 (1) ◽  
pp. 1 ◽  
Author(s):  
JONATHAN W. ARMBRUSTER

Peckoltia contains 12 described species, eight of which are considered valid. Peckoltia arenaria, P. filicaudata, and P. ucayalensis are recognized as synonyms of P. bachi and P. kuhlmanni is recognized as a synonym of P. vittata. In addition, two new species are described. The type species of Peckoltichthys and Sophiancistrus are synonyms of P. bachi and both genera are recognized as junior synonyms of Peckoltia. The species of Peckoltia range throughout much of the Amazon basin, the upper Orinoco, the upper Essequibo, and perhaps the Maroni, and can be identified from most other ancistrins by having dentaries that form angle of 90° or less and from others with angled dentaries by lacking the synapomorphies of those genera. The species of Peckoltia vary from one another mostly in coloration. Peckoltia braueri, P. caenosa n. sp., P. cavatica and P. vittata lack spots on the head while the other species have them. Peckoltia braueri and P. cavatica have orange bands in the dorsal and caudal fins and have the bones and plates of the head and nape outlined in black (vs. no orange bands and head plates and bones not outlined in black in P. caenosa and P. vittata). Peckoltia caenosa has a color pattern consisting of dark vermiculations on the head and abdomen (vs. saddles or blotches on the head and faint dark spots on the abdomen in P. vittata). Among the species with spots on the head, P. lineola n. sp. and P. vermiculata have some of the spots combining to form vermiculations (vs. spots free in P. bachi, P. brevis, P. furcata, and P.oligospila) with the vermiculations larger than the pupil in P. lineola and narrower in P. vermiculata and the vermiculations radiating from a central point in P. vermiculata vs. no such pattern in P. lineola. Peckoltia bachi can be identified from the other species by having widened pelvic-fin spines that can be pulled ventrally such that they are completely ventral and parallel to the body (vs. pelvic-fin spines narrow and cannot be adducted ventral to body) and by having the eye low on the head (vs. high). Peckoltia brevis can be identified from P. furcata and P. oligospila by having well-developed dorsal saddles (vs. saddles faint), no spots on the body behind the nape (vs. spots generally present behind the nape); from P. oligospila by having bands in the caudal fin (vs. spots); and from P. furcata by having the lower caudal-fin spine longer than the upper (vs. upper spine longer). Peckoltia furcata can be identified from P. oligospila by having the upper caudal-fin spine longer than the lower (vs. lower spine longer) and by having bands in the caudal fin (vs. spots). Ancistrus yaravi had been recognized as a species of Peckoltia. The type of A. yaravi is lost, but the original description suggests that the species is the senior synonym of Neblinichthys roraima. A revised morphological phylogeny demonstrates the lack of support for Peckoltia and Hemiancistrus as monophyletic, and phenetic definitions are provided for the two genera. The phylogeny also demonstrates a lack of support of the genus Watawata.


BMC Zoology ◽  
2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Ansa E. Cobham ◽  
Christen K. Mirth

Abstract Background Organisms show an incredibly diverse array of body and organ shapes that are both unique to their taxon and important for adapting to their environment. Achieving these specific shapes involves coordinating the many processes that transform single cells into complex organs, and regulating their growth so that they can function within a fully-formed body. Main text Conceptually, body and organ shape can be separated in two categories, although in practice these categories need not be mutually exclusive. Body shape results from the extent to which organs, or parts of organs, grow relative to each other. The patterns of relative organ size are characterized using allometry. Organ shape, on the other hand, is defined as the geometric features of an organ’s component parts excluding its size. Characterization of organ shape is frequently described by the relative position of homologous features, known as landmarks, distributed throughout the organ. These descriptions fall into the domain of geometric morphometrics. Conclusion In this review, we discuss the methods of characterizing body and organ shape, the developmental programs thought to underlie each, highlight when and how the mechanisms regulating body and organ shape might overlap, and provide our perspective on future avenues of research.


The early development of the head and pharynx of Hynobius nebulosus (11.5 to 32 mm long) and retardatus (27 and 37 mm specimens) was investigated in some detail from transverse serial microtome sections. Analysis included the chondrocranium, jaws and hyobranchial skeleton, ossifications, cranial and anterior spinal nerves, musculature, blood system and other associated anatomical features. The structure of the skeletogenous elements in general agreed with earlier descriptions. However, a rudimentary fenestra lateralis nasi is found in the nasal capsule of H. nebulosus , hitherto not reported, and a complete cartilaginous processus pterygoideus, confluent with the trabecula and inner margin of the lamina orbito-nasalis described by Edgeworth (1923 a ), was not extant in any Hynobius specimen. H. retardatus has a hypoglossal foramen (and nerve) and joins H. nebulosus (Fox 1957), Cryptobranchus japonicus and alleghaniensis as the only living Amphibia to possess this structure. The neural arch homology of the occipital crest is reaffirmed. The columella stilus of the 32 mm H. nebulosus is confluent with the pterygo-quadrate cartilage and because the hyoid and columella have a common blastematous origin in Hypogeophis (Marcus 1910), it is suggested that there was an ancestral cartilaginous continuity between the hyoid and pterygo-quadrate cartilage, similar to the commissura terminales of the branchiale. This feature would further emphasize the branchial segmental homologies of the mandibular cartilage, hyoid and branchiale. The pattern of the cranial nerves is similar to that of other urodele larvae and the arrangement of the profundus and maxillaris nerves supports the view of the descent of urodeles from porolepiforme crossopterygians (Jarvik 1942). There is a segmental series of eleven head-pharynx segments, a complete branchial segment including a levator muscle, nerve, cartilage bar and gill cleft. Each post-hyoid segment is complete except for the absence of branchiale V and VI, and behind the fourth functional gill cleft there are three vestigial blind ones and then the larynx and trachea leading to the lungs. The masseter (2nd segment), digastricus (3rd segment), dilator laryngeus (10th segment) and trapezius (11th segment) are considered to be the homologues of the other six intervening levator gill arch muscles. The arytenoid and tracheal cartilages are considered to be branchial bars of the 10th and 11th segments respectively, and the lungs to have developed from gill pouches of the 11th segment which failed to reach the exterior early in vertebrate evolution. The classical view of the homology of the laryngo-tracheal skeleton with a branchial bar enunciated by Gegenbaur and Wilder independently in 1892 is therefore upheld; disagreement is merely a numerical one. The basic segmental components of the amphibian head and pharynx are modified in ontogeny by omission, distortion or addition, in order to fit the animal for a terrestrial existence.


2016 ◽  
Vol 14 (4) ◽  
Author(s):  
Rafaela Priscila Ota ◽  
◽  
Lúcia Helena Rapp Py-Daniel ◽  
Michel Jégu ◽  
◽  
...  

ABSTRACT A new Metynnis is described from the rio Negro in Brazil and Venezuela, and from black- or clearwater tributaries in Brazil including the rios Parauari, Uatumã, Trombetas, and Sucunduri (the latter belonging to the rio Madeira basin). The new species can be distinguished readily from all congeners by having a high concentration of dark chromatophores on the lateral line scales. It can be further distinguished by the combination of head length 24.3-27.5% of SL, 13-18 gill-rakers on upper limb and 16-24 gill-rakers on lower limb. The new species is most similar to and likely most closely related to Metynnis hypsauchen . These two species share a similar color pattern, body shape and sexual dimorphism of the anal fin. However, they differ in that M. hypsauchen has a lightly pigmented lateral line. The new species is also distinguished from M. hypsauchen by having 56-65 predorsal scales and 90-104 lateral line scales (vs . 36-54, and 65-82, respectively). A detailed osteological description of the new species is provided.


2013 ◽  
Vol 85 (3) ◽  
pp. 1149-1156 ◽  
Author(s):  
Rodrigo Y. Fujimoto ◽  
Mikaelle S. Neves ◽  
Ruda F.B. Santos ◽  
Natalino C. Souza ◽  
Marcia V.S. do Couto ◽  
...  

A total of 281 specimens of freshwater armored ornamental fish species (Leporacanthicus galaxias, Lasiancistrus saetiger, Cochliodon sp., Hypostomus sp., Pseudacanthicus spinosus, Ancistrus sp. and Rineloricaria cf. lanceolata) were captured at the hydrological basin of Guamá River, Pará, Brazil. The infection by Trypanosoma spp. was inspected. The morphological and morphometric characterization of the parasites and the hematological parameters were determined. Leporacanthicus galaxias and Pseudacanthicus spinosus presented 100% infection prevalence, and the other species showed a variable prevalence of infection. The parasites showed clearly different morphotypes and dimensions, and probably belong to different species. The hematological response to the infection varied with the host. Cochliodon sp. showed no differences between infected and not infected fish. In other species several modifications on some hematological parameters were found, but apparently without causing disease. It is emphasized the possibility of introduction of the parasites in new environments due to the artificial movements of these ornamental fish.


2019 ◽  
Vol 20 (72) ◽  
pp. 360-374 ◽  
Author(s):  
Maria do Socorro Rocha da Silva ◽  
Eduardo Antonio Ríos-Villamizar ◽  
Hillândia Brandão da Cunha ◽  
Sebastião Átila Fonseca Miranda ◽  
Sávio José Filgueiras Ferreira ◽  
...  

The geological diversity of the Amazon Basin, as well as the pluvial regime, influences the characteristics of the waters. To know the water types of the rivers of the Amazon basin, 288 superficial water samples were collected, 94 of them along the Amazon River and 194 in their tributaries, from March 2009 to September 2012. The physical, chemical, and physicochemical properties were analyzed. Rivers with pH between 6.5 and 7.6 and electrical conductivity (40.00 - 80.00 μS cm-1) are water bodies that are influenced by the Andean region (e.g., the Amazon River and some of its right bank tributaries). On the other hand, the rivers with pH in the range of 3.5 to 5.5 and conductivity <30.00 μS cm-1, which are Amazon River’s left bank tributaries, reflect the characteristics of the Guiana Shield. The rivers with pH (6.0 to 7.0), low ionic charge, and conductivity <40.0 μS cm-1, such as the lower Amazon River’s right bank tributaries (Tapajos and Xingu) which are influenced by the Central Brazilian Shield, and also the middle/upper Amazon River’s right bank tributaries (Tefé, Coari and Jutaí).


2005 ◽  
Vol 3 (3) ◽  
pp. 319-328 ◽  
Author(s):  
Sandra E. Favorito ◽  
Angela M. Zanata ◽  
Maria I. Assumpção

Synbranchus lampreia, new species, is described from rio Goiapi, Marajó Island, Pará, northern Brazil. It differs from the other two described species of the genus by its color pattern, which consists of large roundish black blotches scattered over a light brown or yellowish ground pigmentation and presence of inconspicuous brown small spots distributed among the large dark spots. The species is further distinguished from S. marmoratus by a higher number of vertebrae and from S. madeira by a shorter postanal length. Information about reproductive aspects is provided and larval stages are described and illustrated.


2021 ◽  
Vol 19 (4) ◽  
Author(s):  
Cárlison Silva-Oliveira ◽  
Rafaela P. Ota ◽  
Flávio C. T. Lima ◽  
Lúcia Rapp Py-Daniel

ABSTRACT A redescription of Bryconops gracilis is provided, a species poorly known for more than a century. Bryconops gracilis differs from all congeners by having the following combination of features: eight branched pelvic-fin rays, 31-36 anal-fin rays, 15-17 predorsal scales arranged in a regular series, two rows of premaxillary teeth, and 53-60 lateral-line scales. The species was often misidentified as B. alburnoides by sharing an overall elongated body shape, caudal fin yellowish in life, and a high number of lateral-line scales. A diagnosis between B. alburnoides and B. gracilis is provided. The holotype of B. gracilis which for many years had whereabouts unknown, was recovered, examined and illustrated by CT-Scan. Additionally, more detailed information about the type locality, morphology, color pattern (including in living specimens), habitat and distribution pattern of species are provided.


2008 ◽  
Vol 33 (3) ◽  
pp. 490-494 ◽  
Author(s):  
Johan B. Mols ◽  
Paul J. A. Keßler ◽  
Steven H. Rogstad ◽  
Richard M. K. Saunders

Recently published molecular phylogenies of the Annonaceae have confirmed the long-held hypothesis that the large paleotropical genus Polyalthia is polyphyletic. Species previously assigned to Polyalthia are now known to belong to up to six distinct, generally well-supported clades. Three members of a group of six species previously referred to as the Polyalthia hypoleuca complex form a monophyletic group (with 99% bootstrap support) that is only distantly related to the other species of Polyalthia sampled. Putative morphological synapomorphies are assessed, and justification provided for validating a new generic name, Maasia. Six species names in the Polyalthia hypoleuca complex are accordingly transferred to Maasia: M. discolor, M. glauca, M. hypoleuca, M. multinervis, M. ovalifolia, and M. sumatrana.


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