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Journal of Paleontology 92(4):611–633 Megaorder Solenata Dall, 1889
Order Hiatellida Carter in Carter et al., 2011 Superfamily Hiatelloidea Gray, 1824 Family Hiatellidae Gray, 1824 Subfamily Panopeinae Bronn, 1862
Genus Panopea Ménard de la Groye, 1807 Type species.—Mya glycimeris Born, 1778 (ICZN, 1986).
Description.—Medium to large, equivalved, quadrate to trape- zoidal, elongate, gaping valves; ligamental nymphs tall; one or two small cardinal teeth; wide pallial sinus. The generic name, Panopea, has been conserved (ICZN, 1986).
Panopea henselli (Hill, 1893) Figure 11.9, 11.10
1893 Pleuromya (?) henselli Hill, p. 31, pl. 4, figs. 1, 2. 1967 Pleuromya (?) henselli; Rodgers in Lokke, p. 127. 1928 Panope (sic) henselli; Adkins, p. 170. 1924 Panopea henselli; Gillet, p. 233. 2002 Panopea henselli; Akers and Akers, p. 473. 1901 Pholadomya henselli; Hill, p. 161. 1937 Panopea hilli; Whitney p. 172, pl. 15, figs. 2, 3.
Lectotype.—Panopea henselli two cotypes NMNH 145646; here the smaller is designated the lectotype.
Diagnosis.—An elongate shell, subcentral beaks, anterior and posterior margins evenly rounded, slight posterior gape; ornament of low, rounded commarginal growth rugae.
Occurrence.—Lower Albian, Somervell County, Texas, about 12m below top of Glen Rose.
Description.—Equivalved, elliptical, elongate valve, umbo subcentral, not prominent; anterior margin rounded, posterior margin subrounded, gaping slightly; angle around beak between dorsal anterior and posterior margins 135°–140°. Ornamented by simple rounded commarginal growth rugae. The average length of the two specimens is 76.1mm; height is 46.95mm; thickness is 33.1mm.
Remarks.—Hill (1893) questioned the generic assignment of this species but created this species because it is characteristic of the Glen Rose Formation. Hill noted the similarities between P. henselli and Thracia myaeformis White (1880). Similar species in Texas Comanchean strata are Panopea texana Shumard 1854 at ‘camp 4 Cross Timbers,’ and Panopea newberryi Shumard 1860 from the Edwards Limestone in north Texas. Both species are illustrated by hand drawings; both are relatively higher than P. henselli. Roemer (1852, p. 45) noted an indeterminate Panopaea (sic) sp. together with Mesorbitolina texana (Roe- mer) near Pedernales that he compared to Panopea regularis d’Orbigny (1843). Panopea sellardsi Whitney 1952 from the middle part of the Glen Rose Formation in central Texas is much smaller than P. henselli, narrower posteriorly, and relatively more inflated.
Panopea is a common genus in pre-Albian strata in
Switzerland and in Argentina (Weaver, 1931). Panopea dupiana d’Orbigny 1843 is about twice as long as high and the umbo is closer to the anterior margin than in P. henselli.
Panopea neocomiensis (Leymerie, 1842) is ornamented by very fine radial striae. Modern Panopea bivalves have aragonite shells that dissolve quickly following death, leaving external molds, which are filled with fine crystalline carbonate. Because of this taphonomy, the resulting casts show mainly external characters.
Conclusions
Species of Pholadomyidea are common and relatively diverse in Albian–lower Cenomanian Comanchean strata in Texas and northern Mexico. Some 22 species have been classed with Pholadomya, Homomya, Pachymya, Myopholas, Panopea, and Pleuromya. Two genera most commonly reported are Homo- mya, order Pholadomyoida, superfamily Pholadomyoidea and Pleuromya, order Pholadida, superfamily Pleuromyoidea. Since 1852, more than a dozen species have been identified as either Homomya or Pleuromya. Because valve morphologies of the two genera are similar in many ways, casts are difficult to separate. Statistical analysis of height and width objectively differentiates species. Eight species are retained in Homomya, four are synonymized with these; two species are provisionally retained in “Homomya” although they differ significantly. Homomyid species in Texas and Mexico range from lower
Albian to lower Cenomanian. They are found in each of three Gulf Coast Comanchean Series groups: upper Aptian to lower Albian Trinity Group, middle to basal upper Albian Freder- icksburg Group, and upper Albian to lower Cenomanian Washita Group. They evolved across this interval, and their ranges vary from one to two million years to up to eight million years. Two sets of species form two clades, the smaller-sized H. knowltoni, H. tarrantensis, H. tlahualiloensis, H. kellumi (Fig. 4) and the larger-sized set of H. cymbiformis,H. austinensis, H. vulgaris,H.budaensis,and H.
auroraensis.Two end-member morphotypes are represented by the ‘streamlined’ Homomya knowltoni, which is an elongate, slightly inflated form with a relatively high umbo, and the cylindrical Homomya budaensis, which is a very elongate, tubular, inflated form with a very low umbo. These infaunal suspension feeders occupied offshore cal- careous mud and carbonate shelf substrates.
Acknowledgments
G. Heumann, Sammlungsverwaltung Paläontologie & Goldfuß-Museum, Steinmann-Institut, Paläontologie, Bonn, kindly provided new photographs of Roemer’s type specimen of Homomya alta. M.S. Florence, Museum Specialist, Smithso- nian Institution, arranged loan of Hill’s types of Pholadomya knowltoni and Pleuromya (?) henselli. A. Molineux and A. Thompson, Non-vertebrate Paleontological Laboratory, Uni- versity of Texas, hosted our visit to the museum and facilitated loan of M.I. Whitney’s specimens and access to the complete Cretaceous collections. D. Miller, University of Michigan Museum of Paleontology, hosted our visit to the museum and arranged loan of Perkins’s types. New photographs of the
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