The megatooth shark, Otodus megalodon, is widely accepted as the largest macrophagous shark that ever lived; and yet, despite over a century of research, its size is still debated. The great white shark, Carcharodon carcharias, is regarded as the best living ecological analog to the extinct megatooth shark and has been the basis for all body length estimates to date. The most widely accepted and applied method for estimating body size of O. megalodon was based upon a linear relationship between tooth crown height and total body length in C. carcharias. However, when applying this method to an associated dentition of O. megalodon (UF-VP-311000), the estimates for this single individual ranged from 11.4 to 41.1 m. These widely variable estimates showed a distinct pattern, in which anterior teeth resulted in lower estimates than posterior teeth. Consequently, previous paleoecological analyses based on body size estimates of O. megalodon may be subject to misinterpretation. Herein, we describe a novel method based on the summed crown width of associated fossil dentitions, which mitigates the variability associated with different tooth positions. The method assumes direct proportionality between the ratio of summed crown width to body length in ecologically and taxonomically related fossil and modern species. Total body lengths were estimated from 11 individuals, representing five lamniform species: Otodus megalodon, Otodus chubutensis, Carcharodon carcharias, Carcharodon hubbelli, and Carcharodon hastalis. The method was extrapolated for the largest known isolated upper tooth of O. megalodon, resulting in a maximum body length estimate of 20 m.
Abstract.-This newly described chondrichthyan fauna from the late Miocene Chucunaque Formation of Lago Bayano reveals a prolific and highly diverse assemblage from Panama, and one of the richest shark faunas from the Neotropics. Strontium geochronology indicates an age of 10-9.5 Ma for the chonrichthyan-bearing strata. Field efforts resulted in 1429 identifiable specimens comprising at least 31 taxa, of which at least eight are new to the documented fossil record of Panama. With this information an analysis of functional diversity was conducted, indicating ecosystems dominated by generalist species feeding upon a wide range of organisms, from plankton to marine mammals. A probabilistic approach of paleobathymetric estimation suggests a neritic environment. Previous studies based on foraminifera have suggested that the Chucunaque Formation had a greater Pacific Ocean affinity, making this the first Miocene chondrichthyan fauna described from the Pacific shelf of Panama. However, our geographic comparisons show that this fauna has mixed Caribbean and Pacific biogeographic affinities, which likely supports the previously purported connection between chondrichthyan faunas during the late Miocene.
The teeth of two megatooth macro-predatory shark species (Carcharocles chubutensis and Carcharocles megalodon; Otodontidae, Chondrichthyes) occur within the Miocene Chesapeake Group of Maryland, U.S.A. Definitive separation between all the teeth of Carcharocles chubutensis and Carcharocles megalodon is impossible because a complex mosaic evolutionary continuum characterizes this transformation, particularly in the loss of lateral cusplets. The cuspleted and uncuspleted teeth of Carcharocles spp. are designated as chronomorphs because there is wide overlap between them both morphologically and chronologically. In the lower Miocene Beds (Shattuck Zones) 2-9 of the Calvert Formation (representing approximately 3.2 million years, 20.2-17 Ma, Burdigalian) both cuspleted and uncuspleted teeth are present, but cuspleted teeth predominate, constituting approximately 87% of the Carcharocles spp. teeth represented in our sample. However, in the middle Miocene Beds 10-16A of the Calvert Formation (representing approximately 2.4 million years, 16.4-14 Ma, Langhian), there is a steady increase in the proportion of uncuspleted Carcharocles teeth. In the upper Miocene Beds 21-24 of the St. Marys Formation (representing approximately 2.8 million years, 10.4-7.6 Ma, Tortonian), lateral cusplets are nearly absent in Carcharocles teeth from our study area, with only a single specimen bearing lateral cusplets. The dental transition between Carcharocles chubutensis and Carcharocles megalodon occurs within the Miocene Chesapeake Group. Although this study helps to elucidate the timing of lateral cusplet loss in Carcharocles locally, the rationale for this prolonged evolutionary transition remains unclear.
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