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Manta cephalic lobes are derived from shark labial cartilages, former placoderm quadrates

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A few years ago,
Swenson et al 2018 reported they determined the origin of cephalic fins in cownose rays (Rhinoptera, Fig 1, red) were derived from an anterior subset of the pectoral fin modified for prey capture, detached and separated from the large lateral portion devoted to locomotion (cyan).

Figure 1. Ventral view of Rhinopterus from an old engraving. Colors added here. The cephalic fins (red) are not connected to the pectoral fins (cyan). Rather they originate at the mouth corners, where the quadrate is. These are labial cartilages, as in other sharks, located lateral to the mouth. ” data-image-caption=”

Figure 1. Ventral view of Rhinopterus from an old engraving. Colors added here. The cephalic fins (red) are not connected to the pectoral fins (cyan). Rather they originate at the mouth corners, where the quadrate is. These are labial cartilages, as in other sharks, located lateral to the mouth.

” data-medium-file=”https://pterosaurheresies.files.wordpress.com/2024/01/rhinoptera-ventral588.jpg?w=233″ data-large-file=”https://pterosaurheresies.files.wordpress.com/2024/01/rhinoptera-ventral588.jpg?w=584″ src=”https://pterosaurheresies.files.wordpress.com/2024/01/rhinoptera-ventral588.jpg” alt=”Figure 1. Ventral view of Rhinopterus from an old engraving. Colors added here. The cephalic fins (red) are not connected to the pectoral fins (cyan). Rather they originate at the mouth corners, where the quadrate is. These are labial cartilages, as in other sharks, located lateral to the mouth. ” class=”wp-image-83983″ />

Figure 1. Ventral view of Rhinopterus from an old engraving. Colors added here. The cephalic fins (red) are not connected to the pectoral fins (cyan). Rather the lobes originate at the mouth corners, where the quadrate is/was. These are labial cartilages, as in other sharks, located lateral to the mouth.

That hypothesis is falsified here.
The cephalic lobes originate at the mouth corners, where the quadrate is/was. That homology was not recognized or identified by Swenson et al. In the present hypothesis, the placoderm quadrate becomes the shark labial cartilage (as we learned earlier here) and continues enlarging and becoming more complex and mobile in the ray cephalic fin/lobe. This occurred several times in rays by convergence, each time resulting in a different sort of cephalic lobe.just ‘Rays’ converged in body shape from several different origins according to the LRT.

The present hypothesis can be falsified. It awaits confirmation, refutation or modification by independent workers employing phenomic phylogenetic analyses.

Figure 2. The enigmatic structures surrounding the mouth of Harpacanthus now appear to be cephalic lobes derived from labial cartilages derived from placoderm quadrate. ” data-image-caption=”

Figure 2. The enigmatic structures surrounding the mouth of Harpacanthus now appear to be cephalic lobes derived from labial cartilages derived from placoderm quadrate.

” data-medium-file=”https://pterosaurheresies.files.wordpress.com/2024/01/harpacanthuslabial588.jpg?w=106″ data-large-file=”https://pterosaurheresies.files.wordpress.com/2024/01/harpacanthuslabial588.jpg?w=362″ src=”https://pterosaurheresies.files.wordpress.com/2024/01/harpacanthuslabial588.jpg” alt=”Figure 2. The enigmatic structures surrounding the mouth of Harpacanthus now appear to be cephalic lobes derived from labial cartilages derived from placoderm quadrate.” class=”wp-image-83987″ />

Figure 2. The enigmatic structures surrounding the mouth of Harpacanthus now appear to be cephalic lobes derived from labial cartilages derived from placoderm quadrates.

The understanding that
cephalic lobes/fins in rays are derived from quadrate labial cartilages found in other sharks sheds light on similar structures found in Carboniferous Harpacanthus (Fig 2, Traquair 1886) appearing independently and by convergence due to a unique three-part substructure.

The traditional clade, Batoidea, was dismantled earlier by the LRT

Figure 3. The labial cartilages in the kitefin shark, Dalatias, are shown here in red. ” data-image-caption=”

Figure 3. The labial cartilages in the kitefin shark, Dalatias, are shown here in red.

” data-medium-file=”https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg?w=147″ data-large-file=”https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg?w=503″ src=”https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg?w=503″ alt=”Figure 3. The labial cartilages in the kitefin shark, Dalatias, are shown here in red.” class=”wp-image-84005″ srcset=”https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg?w=503 503w, https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg?w=74 74w, https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg?w=147 147w, https://pterosaurheresies.files.wordpress.com/2024/01/dalatias_licha_skull588.jpg 588w” sizes=”(max-width: 503px) 100vw, 503px” />

Figure 3. The labial cartilages in the kitefin shark, Dalatias, are shown here in red.

Not all sharks retain labial cartilages.
Others, like Dalatias, the seafloor skimming kitefin shark, enlarge those former external quadrates.

References
Bancroft EN 1829. On the Fish known in Jamaica as the Sea-Devil. The Zoological Journal. 4: 444–457.
Fisher RA 2010, revised 2012. Life history, trophic ecology, & prey handling by cow nose ray, Rhinoptera bonasus, from Chesapeake Bay.
Garman S 1884. An Extraordinary Shark. Bulletin of the Essex Institute: 47–55.
Linnaeus C 1758. Systema naturæ per regna tria naturæ, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis. Tomus I. Editio decima, reformata.
Lund R and Grogan E 2004. Five new euchondrocephalan Chondrichthyes from the Bear Gulch Limestone (Serpukhovian, Namurian E2b) of Montana, USA. In G. Arratia, M. Wilson, R. Cloutier (eds.), Recent Advances in the Origin and Early Radiation of Vertebrates 505-531.
Rafineque CS 1810. Indice d’ittiologia siciliana ossia catalogo metodico dei nomi latini, italiani, e siciliani dei pesci, che si rinvengono in Sicilia disposti secondo un metodo naturale eseguito da un appendice che contiene la descrizione di alcuni nuovi pesci siciliani. Opuscolo del signore C.S. Rafinesque Schmaltz. Messina. 70 pp. + 2 plates.
Smith A 1829. Descriptions of new, or imperfectly known objects of the animal kingdom, found in the south of Africa. South African Commercial Advertiser 3: 2.
Swenson JD et al. 2018. How the Devil Ray Got Its Horns: The Evolution and Development of Cephalic Lobes in Myliobatid Stingrays (Batoidea: Myliobatidae). Front. Ecol. Evol, published online November 13, 2018; doi: 10.3389/fevo.2018.00181
Traquair RH 1886. On Harpacanthus, a new genus of Carboniferous Selachian Spines. Journal of Natural History. Series 5. 18(108): 493–496.
White WT et al. 2018. Phylogeny of the manta and devilrays (Chondrichthyes: mobulidae), with an updated taxonomic arrangement for the family. Zoological Journal of the Linnean Society, 2018, 182, 50–75.

wiki/Sarcastic Fringehead
wiki/Harpacanthus
wiki/Manta
wiki/Giant_oceanic_manta_ray
wiki/Whale_shark
sci-news.com/biology/manta-rays-cephalic-lobes.html
wiki/Batoidea

Goodbye Batoidea, another traditional clade invalidated by the LRT


Source: https://pterosaurheresies.wordpress.com/2024/01/29/manta-cephalic-lobes-are-derived-from-shark-labial-cartilages-former-placoderm-quadrates/


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