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Carcharhinus falciformis, the Silky shark, is a medium/large-sized (to 3.5m) circumtropical species. They are deep-water reef-associated/epipelagic usually in waters less than 500m. The species feeds mainly on teleosts (particularly tuna), but also cephalopods and crustaceans. (Ref. Garrick 1982, Compagno 1984, Compagno et al 2005, and FishBase.org.)
The dentition is cutting-clutching in design with moderately broad distally inclined uppers and narrow upright lowers. Teeth (generally) number 15 per quadrate (plus parasymphyseals)2 displaying gradational and dignathic heterodonty.
The upper teeth are characterized by large coarse shoulder (basal crown) serrations that result in a distinct notch when they meet the triangular main cusp (apical portion of crown) with its finer serrations (ref. fig. left); the notch is displayed along the mesial and (more so) distal edges. The roots are well-developed with a strong nutrient groove.
Lower teeth are rather indistinct but vary positionally. Using the above extant specimen (fig. ) as an example:
Anterior-most positions (fig. right) tend to have an erect cusp with incomplete cutting-edges (finely serrate) and limited to the apical half of the crown; in addition the shoulders of these positions begin to display shoulder serrations commencing from the lateral margins and expanding in more distal positions (by the eighth position (fig. left), the shoulders are nearly completely serrate). In the 10th position, the cusp shows a more distal inclination, the "bulged" appearance of the apical cutting-edge is lost and their serrations disappear to the naked-eye. By the 12th position, the mesial cutting edge is complete (root to apex) and the distal distinguished only by a notch (fig. right). This particular file-set may or may not be typical of the species.
Lee Creek Perspective
The Carcharhinus falciformis tooth-design is fairly common in the Miocene of the Chesapeake and Carolinas. Müller (1999: 49, pl 6, fig 12) include these teeth from the Calvert and Pungo River Fms. as C. priscus (AGASSIZ 1843).
Purdy et al (2001: 151) reported five teeth from Pungo River units 2-4 and attributed them to the extant taxon. The teeth are usually fairly small and closely follow the above description of Recent individuals. It should be noted that Recent teeth tend to have a broader cusp relative to height and the distal shoulder meets the main cusp more apically than seen in Pungo examples.
When evaluating a large (i.e., 100) group of collected Pungo River specimens, certain iconic tooth-designs can be readily recognized; however, when attempting to identify all specimens, many teeth become ambiguous.
With C. falciformis, the primary problem for the junior author were the teeth of C. perezii. These teeth are variable and often display distal & mesial notches and enlarged shoulder serrations; similar to the less variable falciformis. The latter's root tends to be more robust and "v"-shaped when contrasted with perezii (ref. fig. ).
Some C. limbatus teeth are also similar to falciformis; in this case the strength of the distal notch and shoulder & main cusp serrations become a determining factor (ref. fig. , stronger in falciformis. Note that the basal perspectives indicate the actual tooth-positions are also different).
Falciformis lineage
In addition to the extant tooth-design, Oligocene deposits of the area include a version with a non-serrate main cusp. Müller (1999: 48-49, pl 6 fig. 7-9) reported this tooth-design from the Old Church (VA) and Ashley (SC) Fms.and attributed it to C. elongatus (LERICHE 1910). These teeth are also found in the Belgrade Fm of North Carolina (BH pers obs) and a single example (Early Miocene, ? reworked Oligocene) from the Lower Pungo River at Lee Creek (JB, ref. fig. ). It is really difficult to understand the tooth-design(s) represented in Leriche's plate XIX, fig 26-30; none are well illustrated and they appear to represent more than one taxon. Somewhere, probably in the European literature) is a proper description for this tooth/dentition-design, but lacking the library and time to address this problem; the website will simply reject elongatus as a valid name and refer the teeth to falciformis-lineage.
Footnotes
1 | Compagno (1984: 470) attributed falciformis to Bibron in Müller & Henle, 1839; FishBase (Dec 2008) attributes the species to simply Müller & Henle, 1839. |
2 | Garrick (1982: 159-165, Fig 74) notes the formula is usually 15:2:15/15:1:15; but can range greatly: 14-16:1-3:14-16 /14-17:1-3:14-17. |
References
Compagno, L.,1984. FAO Species Catalogue, Vol 4, parts 1 & 2 Sharks of the World. United Nations Development Program.
Compagno, L.,1988. Sharks of the Order Carcharhiniformes. Princeton University Press, Princeton, NJ. 486 pp , 35 plates.
Compagno, L,, Dando & M., Fowler, S., 2005. Sharks of the World. Harper Collins, 368 p.
FishBase.org Dec. 2008.
Garrick, J., 1982. Sharks of the Genus Carcharhinus. NOAA Technical Report NMFS Circular 445. 194 pp
Leriche, M. 1910. Les poissons tertiaires de la Belgique. III. Le poissons oligocènes. Mémoires du Musée Royal d'Histoire Naturelle de Belgique, 3: 49-228.
Müller, A. 1999. Ichthyofaunen aus dem atlantischen Tertiär der USA. Leipziger Geowissenschafteb, Leipzig, 9/10: 1-360.
Purdy, R., Schneider, V., Appelgate, S., McLellan, J., Meyer, R. & Slaughter, R., 2001. The Neogene Sharks, Rays, and Bony Fishes from Lee Creek Mine, Aurora, North Carolina. In: Geology and Paleontology of the Lee Creek Mine, North Carolina, III. C. E. Ray & D. J. Bohaska eds. Smithsonian Contributions to Paleobiology, No 90. Smithsonian Institution Press, Washington D.C. pp. 71-202.
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