SIPHONOPIDAE, Bonaparte, 1850
publication ID |
https://doi.org/ 10.1111/j.1096-3642.2012.00838.x |
persistent identifier |
https://treatment.plazi.org/id/03DB87B7-FFE6-FFAA-FEE3-9754FD26679E |
treatment provided by |
Marcus |
scientific name |
SIPHONOPIDAE |
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SIPHONOPIDAE View in CoL ( FIGS 9 View Figure 9 , S18)
The sphenethmoid is substantially more robust in Siphonops annulatus ( Fig. 9A View Figure 9 ) in comparison to Microcaecilia albiceps (Fig. S18A). The main body of the sphenethmoid is relatively short and broad in siphonopids ( Fig. 9A View Figure 9 ), and accounts for less than half of the total length of the sphenethmoid. An expansion is present representing the only ossified portion of the anterolateral processes, but it is weakly developed ( Fig. 9B View Figure 9 ). The dorsomedial process is thin and covered dorsally in M. albiceps (Fig. S18B) and robust and exposed in Si. annulatus ( Fig. 9B View Figure 9 ). In both species the process extends beyond the anterior limit of the lateral walls. The posterior margin of the lateral wall is deeply incised by the anterior margin of the optic foramen ( Fig. 9A View Figure 9 ). The posterior margin of the floor is incised at the midline and concave in outline ( Fig. 9B View Figure 9 ), more so in M. albiceps (Fig. S18B).
The nasal region is divided by a moderately long nasal septum, which is tall in M. albiceps (Fig. S18A) and short in Si. annulatus ( Fig. 9A View Figure 9 ). It terminates as a tall process just posterior to the external naris. The dorsal sutural surface tapers towards the tip, and for the majority of its length the dorsal margin is thin and blade-like ( Fig. 9B View Figure 9 ). The ventral surface is similarly thin for most of its length. A pair of well-developed, tubular sola nasi extends from the anterior surface of the main body ( Fig. 9C View Figure 9 ).
The anterior wall is pierced by two pairs of foramina ( Fig. 9E View Figure 9 ). The ventral pair is displaced somewhat laterally from the midline ( Fig. 9E View Figure 9 ). The dorsal foramina lead to short canals before exiting onto the anterior surface of the sphenethmoid. The anterolateral foramina are incomplete laterally ( Fig. 9D View Figure 9 ).
The antotic wall of the os basale is slightly angled towards the midline anteriorly when viewed dorsally ( Fig. 9B View Figure 9 ), more so in M. albiceps (Fig. S18B). In anterior view the wall is vertical in Si. annulatus ( Fig. 9F View Figure 9 ), but it is dorsolaterally inclined in M. albiceps (Fig. S18F). The dorsal sutural surface is very narrow; however, there is a large expansion over the antotic region in Si. annulatus ( Fig. 9B View Figure 9 ). The anterior margin of the antotic wall is moderately incised by the posterior margin of the oval optic foramen ( Fig. 9A View Figure 9 ). Five foramina perforate the antotic wall ( Fig. 9H View Figure 9 ), and these have the same configuration and transmit the same structures as those of rhinatrematids and dermophiids (referred to here as Pattern 1; Maddin, 2011). The two large foramina that transmit the two trunks of the trigeminal nerve are incompletely differentiated in the specimens of M. albiceps examined (Fig. S18H), possibly indicating immaturity.
The dorsal surface of the otic-occipital complex is tilted posteroventrally and remains broad in Si. annulatus ( Fig. 9B View Figure 9 ), but tapers in width towards the midline to a narrow surface in M. albiceps (Fig. S18B). The fenestra vestibuli is elongate anteroposteriorly ( Fig. 9A View Figure 9 ), and is especially small in Si. annulatus ( Fig. 9A View Figure 9 ). In posterior view the fenestra vestibuli only slightly incises the lateral margin of the otic-occipital complex ( Fig. 9G View Figure 9 ). The occipital condyle projects far beyond the posterior limit of the otic capsule and the large jugular foramen is visible in lateral view ( Fig. 9A View Figure 9 ). The foramen magnum is subcircular in outline ( Fig. 9G View Figure 9 ).
The medial wall of the otic capsule is pierced by four foramina (endo- and perilymphatic foramina, anterior and posterior vestibulocochlear nerve foramina), in the common locations found in all species examined here ( Fig. 9H View Figure 9 ). Variably within the family two or three additional foramina are present along the ventral margin of the otic capsule for the transmission of parts of the medial branch of the vestibulocochlear nerve ( Maddin, 2011).
The anterior margin of the floor of the os basale tapers continuously to a point towards the tip, anterior to an abrupt constriction in Si. annulatus ( Fig. 9C View Figure 9 ). The tip extends to contact the ventral surface of the nasal septum. A median posterior depression is present and well defined ( Fig. 9F View Figure 9 ). Lateral to the antotic wall is the well-developed basicranial articulation ( Fig. 9A View Figure 9 ). In ventral view the lateral margin of the floor of the os basale is slightly constricted medially, towards the level of the carotid foramina (arrowhead; Fig. 9C View Figure 9 ), and slightly more so in M. albiceps (Fig. S18C). A weak ventral projection is present on the ventral surface of each otic capsule, although this is very poorly developed in M. albiceps (Fig. S18C). The posterior margin of the floor of the os basale terminates at a rounded point, the apex of which closely approaches the ventral margin of the foramen magnum.
The foramen leading to the canal for the carotid artery enters the floor of the os basale anterior to the otic capsule ( Fig. 9C View Figure 9 ) and bifurcates, resulting in lateral and medial canals. The canals terminate in foramina located ventral to the antotic foramina.
The footplate of the stapes is elongate anteroposteriorly, and its long axis is orientated slightly anteroventrally as in Si. annulatus ( Fig. 9I, J View Figure 9 ) to horizontally (Fig. S18I, J). It is also very small and bears a large anterior articular surface in Si. annulatus . The columellar process of the stapes extends roughly horizontally from the lateral surface of the footplate. A weak ridge is present on the process of M. albiceps towards its distal tip (Fig. S18I). There is no foramen present in the base of the columellar process.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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