Browsing by Author "Meylan, Peter A. (Peter Andre)"
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Item Caninemys, a new side-necked turtle (Pelomedusoides, Podocnemididae) from the Miocene of Brazil. (American Museum novitates, no. 3639)(2009) Meylan, Peter A. (Peter Andre); Gaffney, Eugene S.; Campos, Diógenes de Almeida.A new genus and species of podocnemidid pleurodire, Caninemys tridentata, is described on the basis of a skull collected by L.I. Price in 1962 from the late Miocene of Acre, Brazil. It is unique among podocnemidids (and all other turtles) in having greatly inflated maxillae, each with a ventral, toothlike process. Along with a midline process of the premaxillae, these processes form a tridentate condition in the upper triturating surface, also unique among podocnemidids but comparable to the condition in the kinosternid Claudius. This skull has previously been identified as the shell-based genus Stupendemys, but there are no associations supporting this assignment. The type specimens are separated by over 2000 km, and other large podocnemidid taxa are known from this time and region. Although relatively large with a condylobasal skull length of about 17 cm, Caninemys was probably about half the size of Stupendemys. Phylogenetic analysis of 63 skeletal characters provides evidence that this new taxon nests within the family Podocnemididae as follows: (Bauruemys (“Roxochelys” (Podocnemis (Caninemys (Dacquemys ((Erymnochelys, Peltocephalus) (Neochelys (Shweboemys, Stereogenys)))))))).Item The ecology and migrations of sea turtles. 8, Tests of the developmental habitat hypothesis. (Bulletin of the American Museum of Natural History, no. 357)(American Museum of Natural History., 2011-08-10) Meylan, Peter A. (Peter Andre); Meylan, Anne Barkau.; Gray, Jennifer A.The existence of ontogenetic shifts in habitat by marine turtles, and of immature-dominated assemblages in "developmental habitat," were important concepts first proposed by Archie Carr in 1956. Results of long-term, in-water capture programs in Caribbean Panama (17 yr) and Bermuda (37 yr) allow the testing and refinement of these ideas, in particular the developmental habitat hypothesis for Chelonia mydas, Eretmochelys imbricata, and Caretta caretta. A literature survey reviews worldwide studies on these species, and also incorporates Lepidochelys kempii. The studies in Panama and Bermuda reported in this paper use netting, mark/recapture, laparoscopy, and satellite telemetry to investigate size distributions, maturity status, residency, site fidelity, and developmental migrations of three species of sea turtles at three study sites. Characteristics of benthic developmental habitat of C. mydas, E. imbricata, L. kempii, and, to a lesser extent, C. caretta in the Atlantic Ocean usually include benthic feeding; exclusive or nearly exclusive occupation by immature animals; seasonal or multiyear residency and site fidelity in specific areas; developmental migration from the habitat before maturation; and high genetic diversity. Variation of these traits worldwide, contradictory evidence regarding the concept of developmental habitat, and evolution of this life stage are presented. Laparoscopic data provide information concerning the process of sexual maturation; mean size and size range are presented for three maturity stages of C. mydas from Panama and Bermuda, and for size at onset of puberty and maturity for Eretmochelys and Caretta in the West Atlantic. Nicaragua is the primary site of recovery of immature green turtles tagged in Bermuda, representing a developmental migration of at least 2800 km. To the extent that tag returns and stranding data represent good proxies for mortality, transitions between life stages appear to be periods of decreased survivorship.Item Evolution of the side-necked turtles : the families Bothremydidae, Euraxemydidae, and Araripemydidae ; Bulletin of the American Museum of Natural History, no. 300(New York, NY : American Museum of Natural History, 2006) Gaffney, Eugene S.; Tong, Haiyan.; Meylan, Peter A. (Peter Andre)Although pleurodires have been considered significantly less diverse than their sister group, the cryptodires, current discoveries show that pleurodires had a more complex and extensive evolutionary history than had been realized. Previously unknown radiations, particularly in the near-shore marine realm, are revealed by taxa with diverse cranial morphology, indicating many different feeding and sensory strategies. The pleurodire group that is changed the most by the new discoveries is its largest group, the hyperfamily Pelomedusoides. The hyperfamily Pelomedusoides now consists of the families Pelomedusidae, Podocnemididae, Bothremydidae, Araripemydidae, and Euraxemydidae, new family. The families Bothremydidae, Araripemydidae, and Euraxemydidae, new family, are documented with descriptions of skulls, lower jaws, and shells. The relationships of the family Podocnemididae to its sister taxa Hamadachelys and Brasilemys are recognized by placing them in the epifamily Podocnemidinura. The epifamily Podocnemidinura is the sister group to the family Bothremydidae, and together they form the superfamily Podocnemidoidea. The family Araripemydidae consists of one taxon, Araripemys barretoi, from the Aptian-Albian of Brazil. Description of new cranial material suggests that it is the sister group to all other Pelomedusoides or the sister group to the Pelomedusidae, but these relationships are only weakly supported. There is strong support for a multichotomy of Araripemys, Pelomedusidae, and remaining Pelomedusoides. Araripemys is characterized by very thin triturating surfaces and by a shell that lacks mesoplastra and has the first costals reaching the shell margin. The new family Euraxemydidae consists of two new genera: Euraxemys essweini, n. gen. et sp., from the Albian Santana Formation of Brazil, and Dirqadim schaefferi, n. gen. et sp., from the Cenomanian Kem Kem beds of Morocco. Members of the Euraxemydidae are united by the unique possession of a medial process of the quadrate partially covering the prootic and narrowly contacting a ventral process of the exoccipital, in contrast to all other pleurodires, which have either complete exposure or complete covering of the prootic ventrally. Furthermore, members have a ventral process of the exoccipital that is exposed at the lateral margin of the basioccipital in an elongate foot. The Euraxemydidae is hypothesized as the sister group to the superfamily Podocnemidoidea. The family Bothremydidae and the epifamily Podocnemidinura (consisting of the family Podocnemididae, Hamadachelys, and Brasilemys) are united as the superfamily Podocnemidoidea based on the possession of a quadrate-basioccipital contact, the complete or nearly complete ventral covering of the prootic, and the extension of the pectoral scales onto the entoplastron. The family Bothremydidae is a large and diverse group extending from the Albian to the Eocene in North and South America, Europe, Africa, and India. Its monophyly is supported by the presence of a wide exoccipital-quadrate contact, a eustachian tube separated from the incisura columellae auris usually by bone to form a bony canal for the stapes, absence of a fossa precolumellaris, a supraoccipital--quadrate contact (except in the tribe Taphrosphyini), and a posterior enlargement of the fossa orbitalis. Although there is a diversity of triturating surfaces within the family, primitively bothremydids have a posteriorly wide triturating surface with a significant palatine contribution in the upper jaw. The family Bothremydidae consists of four newly recognized, monophyletic groups: the tribes Kurmademydini, Cearachelyini, Bothremydini, and Taphrosphyini. The tribe Kurmademydini consists of two taxa: Kurmademys kallamedensis, from the Maastrichtian Kallamedu Formation of India, and Sankuchemys sethnai, from the Maastrichtian Intertrappean beds of India. The tribe Kurmademydini is characterized by extensive temporal and cheek emargination, a large fossa precolumellaris, and a small, anterior exposure of the prootic on the ventral surface. The tribe Kurmademydini is the sister group to the subfamily Bothremydinae (consisting of the tribes Cearachelyini, Bothremydini, and Taphrosphyini). Members of the subfamily Bothremydinae all possess a foramen stapedio-temporale that faces anteriorly. The tribe Cearachelyini consists of Cearachelys placidoi, from the Albian Santana Formation of Brazil, and Galianemys emringeri and Galianemys whitei, both from the Cenomanian Kem Kem beds of Morocco. The tribe Cearachelyini is characterized by a jugal retracted from the orbital margin and a fenestra postotica formed into a short slit. The tribe Cearachelyini is the sister group to the infrafamily Bothremydodda (consisting of the tribes Bothremydini and Taphrosphyini). The infrafamily Bothremydodda is characterized by a quadrate shelf formed below the cavum tympani, a foramen stapedio-temporale and foramen nervi trigemini that are very close together on the anterior face of the otic chamber, and a condylus occipitalis and occipital neck that are formed only by the exoccipitals. The tribe Bothremydini consists of Foxemys mechinorum, from the Campanian-Maastrichtian of France; Polysternon provinciale, from the Campanian of Europe; Zolhafah bella, from the Maastrichtian Dakla Formation of Egypt; Rosasia soutoi, from the Campanian-Maastrichtian of Portugal; Araiochelys hirayamai, n. gen. et sp., from the Danian phosphates of Ouled Abdoun Basin, Morocco; Bothremys cooki, from the Maastrichtian Navesink Formation of New Jersey; Bothremys maghrebiana, n. sp., from the Danian phosphates of Ouled Abdoun Basin, Morocco; Bothremys kellyi, n. sp., from the Ypresian phosphates of Ouled Abdoun Basin, Morocco; Bothremys arabicus, from the Santonian of Jordan; Chedighaii hutchisoni, n. gen. et sp., from the Campanian Kirtland Formation of New Mexico; and Chedighaii barberi, n. gen., from the Campanian of Arkansas, Alabama, Kansas, and New Jersey. The tribe Bothremydini is the sister group to the tribe Taphrosphyini. The tribe Taphrosphyini is characterized by the presence of a jugal-quadrate contact, the absence of a maxilla-quadratojugal contact, and the absence of a supraoccipital-quadrate contact. Members of the tribe Taphrosphyini have a considerable variety of triturating surfaces but they lack the wide, triangular surfaces typical of the other bothremydids. The tribe Taphrosphyini consists of Taphrosphys sulcatus, from the Danian Hornerstown Formation of New Jersey; Taphrosphys congolensis, from the Paleocene of Cabinda, west Africa; Taphrosphys ippolitoi, n. sp., from the Danian phosphates of the Ouled Abdoun Basin, Morocco; Labrostochelys galkini, n. gen. et sp., from the Danian phosphates of the Ouled Abdoun Basin, Morocco; Phosphatochelys tedfordi, from the Ypresian phosphates of the Ouled Abdoun Basin Morocco; Ummulisani rutgersensis, n. gen. et sp., from the Ypresian phosphates of the Ouled Abdoun Basin, Morocco; Rhothonemys brinkmani, n. gen. et sp., from the Paleogene phosphates of the Ouled Abdoun Basin, Morocco; Azabbaremys moragjonesi, from the Paleocene Teberemt Formation of Mali; Nigeremys gigantea, from the Maastrichtian of Niger; and Arenila krebsi, from the Maastrichtian Dakla Formation of Egypt. Among the Bothremydidae, the Taphrosphyini is the most diverse morphologically. The triturating surfaces show a wide range of variation. The long, narrow skull of Labrostochelys differs significantly from the very short skull of Phosphatochelys. Other genera, such as Azabbaremys and Arenila, have large and massive skulls, but without broadly expanded triturating surfaces, while Ummulisani has very narrow and deep labial ridges. The nasal regions of Taphrosphyini also show wide diversity. Rhothonemys has nasal openings and cavities more than twice the size of the orbits, but the nasal openings in Labrostochelys are smaller than the relatively small orbits. This diversity of Taphrosphyini skull morphology is mostly evident in the Paleogene of North Africa. A phylogenetic analysis of the core dataset of 41 taxa, 122 cranial characters, and 52 postcranial characters relies on comparative descriptions of these taxa. The analysis using PAUP results in one most parsimonious cladogram of 382 steps with a consistency index of 0.6. A Bremer decay analysis shows that the family Bothremydidae is strongly supported at five steps: the tribes Kurmademydini and Cearachelyini have an index of 2, and the tribe Taphrosphyini has an index of 3. The tribe Bothremydini becomes unresolved at one step and is the most weakly supported of these groups. The addition of selected shell-only taxa with low missing data values to the core dataset results in one equally parsimonious cladogram that is resolved as: (Proterochersis (Platychelyidae (Dortoka (Chelidae (Pelomedusidae + Araripemys) (Euraxemydidae (Teneremys (Podocnemididae + Hamadachelys + Brasilemys (Bothremydidae)))))))). A partitioned dataset consisting only of cranial characters (excluding all shell-only taxa) results in one equally parsimonious cladogram identical to the most parsimonious cladogram resulting from the whole dataset; however, a partitioned dataset consisting only of postcranial characters (excluding all skull-only taxa) resulted in 2704 trees, the consensus of which lacks resolution for nearly all Pelomedusoides, but which does resolve more basal pleurodires. When the skull morphology of the Bothremydidae is placed in the context of all other turtles, it becomes apparent that this family has the greatest range of skull forms of any turtle family yet known. In fact, the skull morphologies of many turtle families seem remarkably uniform in comparison (e.g., Testudinidae, Kinosternidae, Pelomedusidae, Trionychidae, Carettochelyidae)...Item Evolution of the side-necked turtles : the family Podocnemididae. (Bulletin of the American Museum of Natural History, no. 350)(American Museum of Natural History., 2011) Gaffney, Eugene S.; Meylan, Peter A. (Peter Andre); Wood, Roger Conant.; Simons, Elwyn L.; Campos, Diógenes de Almeida.The family Podocnemididae consists of 20 genera and 30 species considered here as valid and diagnosable by cranial characters. Three of these genera and eight species persist into the Recent fauna, barely reflecting the evolutionary diversity and distribution of the group. The family extends from the late Cretaceous to the Recent and occurs in North and South America, Europe, Asia, and Africa. A phylogenetic analysis utilizes 31 podocnemidid taxa (30 named and one unnamed; a total of 37 taxa analyzed includes outgroups) in the Podocnemididae that are analyzed using PAUP. The resulting consensus of nine equally parsimonious cladograms is the basis for a new classification of the family. The family Podocnemididae is reconfirmed as monophyletic, using the unique possession of a cavum pterygoidei formed by the basisphenoid, pterygoid, prootic, and quadrate, underlain by the pterygoid and basisphenoid, among other characters. Much of our resolution agrees with that of França and Langer (2006), which can be modified and restated as follows: (Bauruemys (vilavilensis (Podocnemis (Peltocephalus, Erymnochelys)))). The two clades proposed by Broin (1991) and Lapparent de Broin (2000b, 2001, 2003a, 2003b), designated by her as the "subfamily Podocnemidinae" and the "subfamily Erymnochelinae," are inconsistent with our analysis. In our analysis the "Podocnemidinae" (sensu Broin, 1991) is paraphyletic, and the "Erymnochelinae" (sensu Broin, 1991) could be made monophyletic, with the important addition of Peltocephalus (placed in the "Podocnemidinae" by Broin). We add a number of new taxa to the basal Podocnemididae and to the broad-jawed subtribe Stereogenyina. Within the family Podocnemididae Cope, 1868, the sister taxon to all other podocnemidids and recognized as the subfamily Bauruemydinae, new, is Bauruemys elegans (Suárez, 1969a), known from associated skulls and shells. All other podocnemidids, the redefined subfamily Podocnemidinae Cope, 1868, are united by a slight to absent temporal emargination, a completely closed foramen jugulare posterius, and saddle-shaped cervical centra (modified as a separate state in Erymnochelys). A basal group of Cretaceous-Paleocene podocnemidids that are the sister group to all remaining podocnemidids, here termed the infrafamily Peiropemydodda, consisting of two taxa from the late Cretaceous of Brazil, Peiropemys mezzalirai, n. gen. et sp., and Pricemys caiera, n. gen. et sp., and Lapparentemys vilavilensis (Broin, 1971), n. gen., from the Paleocene of Bolivia. The resolution of the basal members of the family is: (Bauruemys (Pricemys (Lapparentemys, Peiropemys)) (Infrafamily Podocnemidodda)). The remaining podocnemidids form the infrafamily Podocnemidodda Cope, 1868, new rank, and is characterized by the possession of a cheek emargination that does not reach above the level of the orbit, the medial expansion of the triturating surfaces with a median maxillary ridge present, and the presence of accessory ridges on the triturating surfaces. This group contains the living podocnemidids and a series of extinct forms, including the marine broad-jawed taxa. Within the Podocnemidodda, the genus Podocnemis is the sister group to all the remaining taxa, which is the magnatribe Erymnochelydand. When only the living fauna is considered our results show Podocnemis as the sister taxon to Erymnochelys plus Peltocephalus, in common with Williams (1954c), Franc¸a and Langer (2006), Meylan et al. (2009), and Cadena et al. (2010). With the fossil taxa present, the Erymnochelydand is united only by the small to absent cheek emargination. However, some of the fossil taxa (i.e., Caninemys, Dacquemys), are not known for a number of characters, and, if the analysis is reduced to include only the living species, Erymnochelys and Peltocephalus are united by a greater number of characters: cavum pterygoidei with enlarged anterior opening, so that the foramen cavernosum enters the roof of the cavum pterygoidei, orbits facing anterolaterally, jugal-quadrate contact present, cheek emargination slight to absent, horizontal occipital shelf absent, premaxillae reach apertura narium interna (also in some Podocnemis), supraoccipital roof exposure slight or absent, chorda tympani enclosed in processus retroarticularis, neural series extends to costal six, and axillary musk duct not in bridge. When one considers just the Recent genera, none of the published molecular results reproduce the Gaffney and Meylan (1988) and Lapparent de Broin (2000b) resolution of (Erymnochelys (Podocnemis, Peltocephalus)); rather these publications show a preference for the (Peltocephalus (Podocnemis, Erymnochelys)) arrangement, while we, in agreement with Franc¸a and Langer (2006) and the earlier version of the present data set, Meylan et al. (2009), place our marbles with the third alternative, (Podocnemis (Peltocephalus, Erymnochelys)). This latter hypothesis has a number of characters favoring its resolution, even when fossils are excluded. One of the more compelling ones is the large cavum pterygoidei with an enlarged anterior opening and the foramen cavernosum containing the lateral head vein, entering the roof of the cavum pterygoidei. Within the magnatribe Erymnochelydand are the following taxa: Caninemys, Dacquemys, unnamed genus UCMP 42008, Albertwoodemys, Turkanemys, Peltocephalus, Erymnochelys, Neochelys, Papoulemys, and the members of the tribe Stereogenyini (see below). The resolution of Caninemys within the Erymnochelydand is not strongly supported; in only one step it becomes a multichotomy with Podocnemis and the infrafamily Peiropemydodda. Neochelys, Papoulemys (possibly a synonym of Neochelys), and Dacquemys, however, are strongly supported as part of the magnatribe Erymnochelydand, as proposed earlier (Broin, 1991; Lapparent de Broin, 2000b, 2001, 2003a, 2003b). A new shell-based taxon, Albertwoodemys testudinum, n. gen. et sp., and an unnamed skull and shell, UCMP 42008, are united by a high-domed shell with thick lateral ridges along the plastron and the absence/fusion of the pectoral scales. The skull of UCMP 42008 agrees with that in Dacquemys in having large parietals and a supraoccipital covering the posterior margin. Lacking a skull, Albertwoodemys is not entered into the data set, but the skull-shell specimen of the closely related UCMP 42008 is in the analysis. New skull material identifiable as Neochelys has been discovered associated with shells of ‘‘Podocnemis’’ fajumensis Andrews, 1903, resulting in the new combination Neochelys fajumensis (Andrews, 1903). Neochelys has the Erymnochelydand synapomorphy of a large cavum pterygoidei with an enlarged anterior opening and the foramen cavernosum entering the roof of the cavum pterygoidei, as in Peltocephalus and Erymnochelys. The European Neochelys species are Eocene and the African Fayum species is Early Oligocene, extending both spatial and temporal ranges of the genus. The tribe Stereogenyini has a dorsal process of the palatine that reaches the frontal in the septum orbitotemporale, the fossa precolumellaris is absent, and both foramina nervi hypoglossi are combined and recessed in a short canal that opens on the occipital surface. Within the tribe Stereogenyini, Mogharemys blanckenhorni Dacque´ (1912), n. gen., is the sister taxon to the welldefined subtribe Stereogenyina. Two groups are recognized within the subtribe Stereogenyina. The infratribe Bairdemydita contains Bairdemys Gaffney and Wood, Latentemys plowdeni, n. gen. et sp., Cordichelys antiqua (Andrews, 1903), n. gen. The infratribe Stereogenyita contains Brontochelys gaffneyi (Wood, 1970), n. gen., Lemurchelys diasphax, n. gen. et sp., Shweboemys Swinton, 1939, and Stereogenys Andrews, 1901. The subtribe Stereogenyina is strongly supported by a secondary palate with a median cleft, unique among turtles, as well as other characters. While the other Podocnemididae were apparently freshwater species, there is evidence that many or all of the subtribe Stereogenyina were marine or near-shore marine. Compared with a group such as the Bothremydidae, we see in the evolution of the Podocnemididae, a relatively conservative series of South American paraphyletic taxa with an unusually persistent cranial as well as shell morphology, beginning in the Late Cretaceous with Bauruemys, Peiropemys, and Pricemys, and continuing with the Paleocene Lapparentemys, culminating in the Recent Podocnemis. A monophyletic Tertiary group with more geographic, taxonomic, and morphologic diversity, the magnatribe Erymnochelydand, contains African, European, Asian, and South American taxa, as well as a radiation of marine, broad-jawed species in the mid-Tertiary. The living remnants of the Erymnochelydand are the South American Peltocephalus and the African Erymnochelys, close relatives despite their current geographic separation.Item Galianemys, a new side-necked turtle (Pelomedusoides, Bothremydidae) from the late Cretaceous of Morocco. American Museum novitates ; no. 3379(New York, NY : American Museum of Natural History, 2002) Gaffney, Eugene S.; Tong, Haiyan.; Meylan, Peter A. (Peter Andre)The Cenomanian redbeds of southern Morocco have yielded skulls of a new genus and two new species of side-necked turtles, Galianemys whitei and Galianemys emringeri. The genus is based on a series of nine well-preserved skulls and three partial skulls. Galianemys is a pelomedusoid pleurodire belonging to the family Bothremydidae Baur, 1891, because it has: (1) precolumellar fossa absent, (2) foramen stapedio-temporale facing anteriorly, (3) eustachian tube separated from stapes by bone, and (4) exoccipital-quadrate contact. Within the Bothremydidae Galianemys is best resolved as the sister group to Cearachelys because both have the jugal retracted from the orbital margin and a small, slitlike fenestra postotica. Galianemys emringeri has a deep fossa pterygoidei, ventrally exposed prootic, foramen nervi facialis and foramen nervi vidiani, a thicker labial ridge, and the jugal not exposed on the triturating surface, while Galianemys whitei has a shallow fossa pterygoidei, covered prootic and foramen nervi facialis and vidiani, a thinner labial ridge, and a jugal exposed on the triturating surface.Item The phylogenetic relationships of soft-shelled turtles (family Trionychidae). Bulletin of the AMNH ; v. 186, article 1([New York] : American Museum of Natural History, 1987) Meylan, Peter A. (Peter Andre)"Phylogenetic analysis of 113 characters of the osteology of the 22 living species of trionychid turtles and representatives of all other living turtle families, provides abundant evidence on the relationships of soft-shelled turtles to other turtles and on the interrelationships within the family. These data suggest that the family Trionychidae shares a unique common ancestor with the Dermatemydidae, Kinosternidae, and Carettochelyidae, and that the Kinosternidae share a unique common ancestor with the Trionychidae and Carettochelyidae. Furthermore, it appears that the staurotypine kinosternids are most closely related to the Trionychidae and Carettochelyidae. Carettochelyids and trionychids share numerous unique features and clearly constitute a monophyletic group. Within the Trionychidae, the subfamilies Cyclanorbinae and Trionychinae are recognized as monophyletic clades. Recognition of three cyclanorbine genera, Cycloderma, Cyclanorbis, and Lissemys, is warranted. Within the Trionychinae, four distinct clades are recognized. The Trionyx cartilagineus group includes Chitra indica and Pelochelys bibroni, on the basis of the unique location of the foramen posterior canalis carotici interni, and features of the trigeminal region. The North American group includes T. triunguis, T. euphraticus, T. swinhoei, T. ferox, T. spiniferus, and T. muticus, and can be recognized by the presence of eight or fewer neurals (first and second are fused), deeply emarginate prefrontals, and a large contribution by the parietal to the processus trochlearis oticum. The Indian group includes four species: T. gangeticus, T. hurum, T. leithii, and T. nigricans; all exhibit a free first neural, five plastral callosities, and intermediately extended epiplastra. Lastly, the T. steindachneri group, which includes T. steindachneri, T. sinensis, and T. subplanus, is diagnosed by a descending spine of the opisthotic that divides the fenestra postotica in most specimens. Two equally parsimonious arrangements of the Trionychinae differ in the placement of the North American clade. In one, this clade is the sister group of the T. cartilagineus clade; in the other, it is the sister group of the T. steindachneri clade. In both, the Indian group is paraphyletic and gives rise to the T. steindachneri clade. A revised classification of the family Trionychidae is provided. The use of 2 subfamilies, 6 tribes, and 14 genera is recommended. This expanded taxonomy will more completely reflect the hierarchical relationships that reflect recency of common ancestry as determined by the cladistic analyses"--P. 4.Item Redescription of the skull of Dacquemys Williams, 1954, a podocnemidid side-necked turtle from the late Eocene of Egypt. American Museum novitates ; no. 3372(New York, NY : American Museum of Natural History, 2002) Gaffney, Eugene S.; Deblieux, Donald D.; Simons, Elwyn L.; Sanchez-Villagra, Marcelo R.; Meylan, Peter A. (Peter Andre)The known material of the side-necked turtle Dacquemys paleomorpha Williams, 1954, consists of the type skull and a new skull from the late Eocene of Egypt. Dacquemys is reaffirmed as a member of the Podocnemididae because of its well-developed cavum pterygoideus. Within the Podocnemididae Dacquemys uniquely possesses a fully roofed temporal region produced by a posteriorly extensive parietal and wide supraoccipital, a very wide interorbital area, and two accessory maxillary ridges meeting anteriorly to form an enclosed trough.Item The skeletal morphology of the Cretaceous cryptodiran turtle, Adocus, and the relationships of the Trionychoidea. American Museum novitates ; ; no. 2941.(New York, N.Y. : American Museum of Natural History, 1989) Meylan, Peter A. (Peter Andre); Gaffney, Eugene S.Item The Transylvanian turtle, Kallokibotion, a primitive cryptodire of Cretaceous Age. American Museum novitates ; no. 3040(New York, N.Y. : American Museum of Natural History, 1992) Gaffney, Eugene S.; Meylan, Peter A. (Peter Andre)