Myoglanis

Carlos Donascimiento & John G. Lundberg, 2005, Myoglanis aspredinoides (Siluriformes: Heptapteridae), a new catfish from the Río Ventuari, Venezuela., Zootaxa 1009, pp. 37-49 : 44-45

publication ID

z01009p037

publication LSID

lsid:zoobank.org:pub:CC27B747-2338-4221-A174-58F16073C8C6

DOI

https://doi.org/10.5281/zenodo.6267749

persistent identifier

https://treatment.plazi.org/id/DAB76468-4685-CB5E-C7A1-C96C6B2EBC22

treatment provided by

Thomas

scientific name

Myoglanis
status

 

[[ Genus Myoglanis View in CoL View at ENA   ZBK ]]

Discussion

Eigenmann (1912) created the genera Brachyglanis   ZBK , Myoglanis   ZBK and Leptoglanis   ZBK for new species of small catfishes from Guyana. The last of these, being preoccupied by Leptoglanis Boulenger   ZBK (1902), was replaced by Leptorhamdia Eigenmann   ZBK (1918). The fishes in Eigenmann’s genera are similar in having a thick layer of jaw adductor muscle on the skull roof, strong pectoral-fin spines and subcutaneous eyes. As diagnosed by Eigenmann, Brachyglanis   ZBK , Myoglanis   ZBK and Leptorhamdia   ZBK differ primarily in degree of spine-like ossification of the dorsal spine, length of the adipose fin and its contact with the caudal, and caudal-fin shape. The taxonomic histories of Myoglanis   ZBK and Leptorhamdia   ZBK are checkered with their synonymy by Gosline (1941) followed by renewed recognition by Lundberg et al. (1991), Bockmann (1998) and Bockmann and Guazelli (2003).

Brachyglanis   ZBK , Leptorhamdia   ZBK and Myoglanis   ZBK along with Gladioglanis   ZBK and the members of the Nemuroglanis   ZBK subclade (Ferraris 1988) were assigned by Lundberg et al. (1991) to a large unnamed monophyletic group characterized by the loss of a free orbital rim around the eye. This group excludes the genera Brachyrhamdia   ZBK , Pimelodella   ZBK (with its synonyms Caecorhamdella   ZBK and Typhlobagrus   ZBK ), Rhamdella and Rhamdia (including Caecorhamdia   ZBK ). Because of their plesiomorphic retention of a strong pectoral spine Gladioglanis   ZBK , Brachyglanis   ZBK , Leptorhamdia   ZBK and Myoglanis   ZBK are excluded from the Nemuroglanis   ZBK subclade in which the spine is reduced to a segmented, unbranched ray. Moreover, Gladioglanis   ZBK , Leptorhamdia   ZBK and Myoglanis   ZBK each share different synapomorphic characters with the Nemuroglanis   ZBK subclade, the resulting pattern of incongruence resulted in an unresolved arrangement at this level with Brachyglanis   ZBK in a lower level because of its plesiomorphic condition for all of those characters. Lundberg et al. (1991) also advanced a hypothesis of possible monophyly of Brachyglanis   ZBK , Leptorhamdia   ZBK and Myoglanis   ZBK based on the invasion of the adductor mandibulae muscle onto the skull roof, an obvious derived condition for Siluriformes (Lundberg 1982; Grande & Lundberg 1988).

More recently Bockmann (1998) presented a comprehensive hypotheses of phylogenetic relationships and diagnoses for heptapterid genera and higher subgroups. Bockmann (1998) presented phylogenetic evidence for a sister group relationship between Leptorhamdia   ZBK and Myoglanis   ZBK within a clade also including Brachyglanis   ZBK . In our study we located two additional informative characters that corroborate the Leptorhamdia   ZBK - Myoglanis   ZBK pair. First, the anteriormost cutaneous sensory pores of supraorbital (SO1), infraorbital (IO1) and mandibular branch (MA1-3 in Leptorhamdia   ZBK and Myoglanis aspredinoides   ZBK ; MA1-5 in Myoglanis   ZBK sp) are wider than remaining pores. In the case of Myoglanis potaroensis   ZBK only SO1 and IO1 are considerably wider than the others and the pores of preoperculomandibular canal are relatively wide but of similar diameter. A widened condition of cutaneous sensory pores in the head is also found in Gladioglanis   ZBK , but in this case all the pores of each canal exhibit the same diameter and are therefore considered different from the asymmetric condition of Leptorhamdia   ZBK and Myoglanis   ZBK . Second, the anterior margin of first and second pelvic-fin rays are pinnate (Fig. 4), with long anterior extensions of the lepidotrich segments. In Heptapteridae a similar but less developed condition is present in Cetopsorhamdia   ZBK sp., where the lepidotrich segments are restricted to the distal margin. Elsewhere in Siluriformes the glyptosternoid fishes of the family Sisoridae exhibit an extreme pinnate condition both in pectoral and pelvic fins that has apparently evolved independently and is associated with the torrential stream habitat of glyptosternoids (Hora & Silas 1952). Table 2 summarizes these and other characters varying among Myoglanis   ZBK , Leptorhamdia   ZBK and Brachyglanis   ZBK . Thus, in the latest authoritative treatments, Myoglanis   ZBK is considered both valid and monophyletic. Within this framework, the diagnostic synapomorphies of Myoglanis   ZBK are: ossified portion of dorsal spine greatly reduced; first dorsal-fin basal radial inserted posterior to neural spine of vertebra 6; 46 or more total vertebrae (vs. 47 or fewer); 16 or more anal-fin rays (vs. 17 or fewer); lower half or more of adipose fin thickened (vs. base only thickened); adipose fin reaching and broadly confluent with caudal fin (vs. adipose fin not reaching caudal fin or if close adipose retains a free posterior lobe); upper procurrent rays of the caudal fin reduced to 8-13 (vs. 12 or more). Within the genus, M. aspredinoides   ZBK exhibits the most highly derived conditions of total vertebral, dorsal procurrent caudal-fin ray and anal-fin ray counts, and matches its congeners in the dorsal and adipose fin synapomorphies.

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