Evolutionary transitions to marine habitats occurred frequently among Mesozoic reptiles. Only one such clade survives to the present: sea turtles (Chelonioidea). Other marine turtles originated during the Mesozoic, but uncertain affinities of key fossils have obscured the number of transitions to marine life, and the timing of the origin of marine adaptation in chelonioids. Phylogenetic studies support either a highly‐inclusive chelonioid total‐group including fossil marine clades from the Jurassic and Cretaceous (e.g. protostegids, thalassochelydians, sandownids) or a less inclusive chelonioid total‐group excluding those clades. Under this paradigm, these clades belong outside Cryptodira, and represent at least one additional evolutionary transition to marine life in turtles. We present a new phylogenetic hypothesis informed by high resolution computed tomographic data of living and fossil taxa. Besides a well‐supported Chelonioidea, which includes protostegids, we recover a previously unknown clade of stem‐group turtles, Angolachelonia, which includes the Late Jurassic thalassochelydians, and the Cretaceous–Palaeogene sandownids. Accounting for the Triassic Odontochelys, our results indicate three independent evolutionary transitions to marine life in non‐pleurodiran turtles (plus an additional two‐three in pleurodires). Among all independent origins of marine habits, a pelagic ecology only evolved once, among chelonioids. All turtle groups that independently invaded marine habitats in the Jurassic–Cretaceous (chelonioids, angolachelonians, bothremydid pleurodires) survived the Cretaceous–Palaeogene mass extinction event. This highlights extensive survival of marine turtles compared to other marine reptiles. Furthermore, deeply‐nested clades such as chelonioids are found by the middle Early Cretaceous, suggesting a rapid diversification of crown‐group turtles during the Early Cretaceous.
Turtles are a major group of reptiles and show high ecological diversity, inhabiting marine, freshwater and terrestrial environments. The ancestral ecology for crown‐turtles is inferred to be aquatic (Joyce & Gauthier 2004) and there is evidence for variation between terrestrial and aquatic habitats among stem‐group turtles (Joyce & Gauthier 2004; Scheyer & Sander 2007; Li et al. 2008; Reisz & Head 2008; Scheyer et al. 2014; Cerda et al. 2016; Joyce 2017). As an ecologically diverse extant group with an excellent fossil record, turtles provide information on the evolutionary dynamics of ecological transitions in vertebrates, and in particular the secondary reversion to marine life. This transition is not well understood in reptiles, despite its occurrence in at least 18 lineages among many higher groups (mesosaurs, thalattosaurs, ichthyosaurs, sauropterygians, crocodiliforms, rhynchocephalians, squamates, turtles) (Motani 2009; Benson 2013; Bardet et al. 2014). In part, this lack of understanding results from the extinction of most marine reptile groups by the end of the Mesozoic, or mid‐Cenozoic.
Within turtles alone, multiple lineages independently adapted to marine life from as early as the Triassic (Gaffney et al. 2006; Li et al. 2008; Mateus et al. 2009; Anquetin et al. 2015; Ferreira et al. 2015). Of these, only chelonioids (sea turtles) survive to the present. Previous phylogenetic hypotheses imply at least four and as many as eight independent transitions to marine life in turtles, throughout their entire evolutionary history (e.g. Joyce 2007; Li et al. 2008; Mateus et al. 2009; Rabi et al. 2012; Anquetin et al. 2015). However, deep uncertainty regarding the phylogenetic affinities of several extinct groups renders the precise number highly uncertain. This lack of consensus on turtle phylogeny also affects our understanding of wider macroevolutionary dynamics, such as the mode and rate of morphological evolution during ecological transitions.
Extant turtles provide genetic (= molecular) data that help to constrain their phylogenetic relationships and allow the estimation of divergence ages for subclades (e.g. Joyce et al. 2013). Morphological and molecular phylogenies have resulted in different hypotheses for the interrelationships of extant turtles (for instance regarding the monophyly and content of Chelydroidea: Shaffer et al. 1997; Parham et al. 2006; Joyce et al. 2013; Joyce 2016). Although morphological evidence has subsequently been found to support some of the propositions of molecular studies (e.g. Knauss et al. 2011 for the example of Chelydroidea) not all conflicting relationships among crown‐turtles have yet been reconciled. At present, it is common for morphological studies of turtle phylogeny to use a backbone constraint informed by the results of molecular studies (Danilov & Parham 2008; Cadena & Parham 2015; Zhou & Rabi 2015).
Nevertheless, analysis of morphological data remains important, because the placement of fossil taxa has to be established for a reliable tree calibration in molecular clock analyses (Near et al. 2005; Parham et al. 2012; Joyce et al. 2013). Additionally, the consideration of fossils is fundamental to our understanding of the patterns of morphological and ecological evolution during deep divergences, and in entirely extinct groups. This is maybe best documented by the evolutionary transition from fish to tetrapods (e.g. Ahlberg & Milner 1994; Ahlberg et al. 1996; Carroll 1996; Ahlberg & Johanson 1998; Long & Gordon 2004; Clack 2009) and by the dinosaurian origins of birds (Ostrom 1975; Gauthier 1986).
Several Mesozoic turtle groups exemplify the difficulties associated with robustly fitting fossil taxa into the turtle tree. These include the marine thalassochelydians, sandownids and protostegids, as well as the freshwater xinjiangchelyids, sinemydids and macrobaenids. Most of these groups have been alternatively proposed to be stem‐group turtles, stem‐group cryptodires, or within the crown‐group of cryptodires as stem‐ or crown‐group chelonioids, although this is in part caused by the instability of the position of pleurodires across studies (Sterli 2010). Because the placements of these groups influence reconstructions of morphological changes during deep evolutionary divergences, they have implications for the relative phylogenetic placements of other clades. Furthermore, different phylogenetic hypotheses give rise to distinct conclusions regarding: (1) the number of times that marine ecologies have evolved within turtles; (2) the timing of secondarily marine adaptation in the chelonioid total‐group; and (3) inferences of character state changes and polarities, which influence hypotheses of morphological evolution on the stem‐group of cryptodires, and among turtles more widely. Clearly, resolving the phylogeny of key fossil groups can have substantive implications for our understanding of the evolution of turtles as a whole. We present a new phylogenetic analysis that helps to clarify these issues.
Adaptation to marine life evolved independently in stem‐group turtles and in both cryptodires and pleurodires. The stem‐group turtle Odontochelys semitestacea from the middle Late Triassic (220 Ma) is generally interpreted as the oldest marine turtle based on its depositional environment (Li et al. 2008; Reisz & Head 2008; Lyson et al. 2010). Furthermore, Odontochelys has limb proportions characteristic of aquatic turtles, contrasting with other Triassic stem‐turtles (Joyce & Gauthier 2004; Li et al. 2008).
Among pleurodires, marine taxa have been identified in two phylogenetically distinct lineages, documenting at least two independent instances of adaptation to marine life: the Cretaceous–Oligocene (and possibly Miocene) Bothremydidae (Gaffney et al. 2006; Rabi et al. 2012), and the Eocene–Pleistocene Stereogyina (Sánchez‐Villagra et al. 2000; Winkler & Sánchez‐Villagra 2006; Gaffney et al. 2011; Ferreira et al. 2015). Bothremydid phylogeny suggests that there could be two independent origins of marine habits in that group, as the marine Taphrosphyini and the marine Bothremydina do not form a monophyletic group with respect to freshwater bothremydids (Gaffney et al. 2006; Rabi et al. 2012).
The number of independent lineages of marine turtles within the total group of cryptodires is less well understood. Chelonioidea, which includes all extant sea turtles, represents one unambiguous evolutionary origin of secondarily marine ecologies within the crown of cryptodires. Chelonioids form a clade of highly marine‐adapted forms that are characterized by the presence of flippers, salt glands, incipient to well‐developed secondary palates, and a range of modifications of the shell, all of which represent adaptations to a marine lifestyle, and are observed in at least some fossil chelonioids (Mlynarski 1976; Zangerl 1980; Hirayama 1994). Undisputed marine stem‐group chelonioids are also known from that time (Toxochelys spp.: Coniacian–Campanian, Nicholls 1988; Joyce et al. 2013) but the phylogenetic position of some putative crown‐group chelonioids from the Cretaceous (e.g. Allopleuron hofmanni from the late Maastrichtian; Gray 1831) have been uncertain. The only non‐marine turtles that have repeatedly been recovered as stem‐group chelonioids are various ‘macrobaenids’ (usually including Judithemys sukhanovi from the Campanian of Canada; Parham & Hutchinson 2003) and ‘sinemydids’ (Brinkman & Wu 1999; Danilov & Parham 2008; Sterli 2010; Pérez‐García 2012; Cadena & Parham 2015) but most authors argue against this (e.g. Zhou & Rabi 2015).
Other marine turtles have been recognized, especially from the Late Jurassic and Early Cretaceous. Depending on their phylogenetic position, these groups, the protostegids, thalassochelydians and sandownids, could represent additional, independent origins of marine adaptation (Fig. 1). Protostegids are known from the Barremian–Campanian (e.g. Zangerl 1953; Collins 1970; Hirayama 1994, 1998; Hooks 1998; Kear & Lee 2006; Cadena & Parham 2015). Thalassochelydians include ‘plesiochelyids’, ‘eurysternids’, ‘thalassemydids’, Solnhofia parsoni and Jurassichelon oleronensis from the Late Jurassic (e.g. Gaffney 1975a, b; Rieppel 1980; Joyce 2000; Anquetin & Joyce 2014; Anquetin et al. 2014a, b, 2015, 2017). Sandownids are known from the Cretaceous and Palaeogene (Aptian–Danian; Meylan et al. 2000; Mateus et al. 2009; Cadena 2015). Many distinct phylogenetic hypotheses have been proposed, not only for these groups, but also for their members. In the following, we provide brief summaries of all relevant groups, including evidence for their inferred ecologies and previously proposed phylogenetic relationships.Figure 1 Open in figure viewerPowerPoint Simplified phylogenetic hypotheses of selected previous studies highlighting different phylogenetic positions that have been proposed for marine, non‐pleurodiran turtles. A, Joyce (2007). B, Danilov & Parham (2008). C, Sterli (2010). D, Anquetin (2012). E, Tong & Meylan (2013). F, Sterli & de la Fuente (2013). G, Anquetin et al. (2015). H, Cadena & Parham (2015) and Cadena (2015). I, Zhou & Rabi (2015). Note that the colours denote proposed clades, following Anquetin et al. (2017) for Thalassochelydia, Tong & Meylan (2013) for Sandownidae, Cadena & Parham (2015) for Protostegidae, and Rabi et al. (2014) for Sinemydidae/Macrobaenidae. Note that ‘Chelonioidea’ is used to denote the crown‐group herein.
Protostegids are a group of Cretaceous marine turtles with a cosmopolitan distribution (e.g. Zangerl 1953; Collins 1970; Hirayama 1998; Kear & Lee 2006; Cadena & Parham 2015). They include the gigantic forms Archelon ischryos (Wieland 1896) and Protostega gigas (Cope 1871a) from the Campanian of North America, as well as early representatives such as Santanachelys gaffneyi from the late Aptian or early Albian of Brazil (Hirayama 1998) and Desmatochelys padillai from the late Barremian or early Aptian of Colombia (Cadena & Parham 2015). These taxa have been found in a monophyletic group in most phylogenetic studies so far (Hirayama 1994, 1998; Hooks 1998; Kear & Lee 2006; Cadena & Parham 2015; but see Gentry et al. 2018). They share unambiguous adaptations to a pelagic marine lifestyle with chelonioids, including the modification of hands into flippers and the reduction of the shell, and also an enlarged fenestra interorbitale indicative of salt glands (e.g. Wieland 1896, 1906; Case 1897; Hirayama 1998). Many studies have found protostegids on the stem‐lineage of Dermochelys (the extant leatherback turtle; Hirayama 1994; Kear & Lee 2006; Bardet et al. 2013; Cadena & Parham 2015; Gentry et al. 2018) with a few exceptions (Joyce 2007; Anquetin 2012; and studies expanding these matrices; see below).
Thalassochelydians (sensu Anquetin et al. 2017) are an assemblage of Late Jurassic turtles from central and western Europe (Anquetin & Chapman 2016; Anquetin et al. 2017), and possibly Argentina (Fernández & de la Fuente 1988; de la Fuente & Fernández 2011). They are exclusively found in marine depositional environments, with ‘plesiochelyids’ and ‘thalassemydids’ found in sediments indicating open‐marine carbonate platform environments, and ‘eurysternids’ such as Solnhofia parsoni coming from more marginal marine settings (Anquetin et al. 2017). Plesiochelyids have been found as a monophyletic group by almost all phylogenetic studies (e.g. Sterli 2010; Sterli & de la Fuente 2013; Anquetin et al. 2015; but see Anquetin 2012) but the monophyly of the more inclusive Thalassochelydia (including Solnhofia parsoni, Jurassichelon oleronensis and plesiochelyids) has only recently been demonstrated (Anquetin et al. 2015; but see below). The marine habits of these taxa are supported by their oxygen isotope signatures, which indicate brackish environments for ‘eurysternids’ and fully marine environments for ‘plesiochelyids’ (Billon‐Bruyat et al. 2005). Unlike chelonioids and protostegids, thalassochelydian limbs do not take the form of flippers, although their manus is notably elongated, indicating adaptation to aquatic locomotion (Anquetin et al. 2017). Furthermore, an expanded fenestra interorbitale indicates the presence of salt glands, and the presence of shell fontanelles provides morphological evidence consistent with a marine lifestyle (Anquetin et al. 2017). The shell bone histology is also consistent with an aquatic lifestyle (Scheyer et al. 2014).
Sandownids are a secondarily marine group of putative stem‐group cryptodires currently known from four taxa ranging in age from the Aptian (Sandownia harrisi; Meylan et al. 2000) or possibly late Barremian (Leyvachelys cipadi; Cadena 2015) to the Paleocene (Brachyopsemys tingitana; Tong & Meylan 2013). These taxa have been recovered as a clade by all phylogenetic studies that included more than one of them (Mateus et al. 2009; Tong & Meylan 2013; Cadena 2015). Their fossils come from shallow marine deposits, and distinctive morphological adaptations such as their extensive secondary palate indicative of a durophagous diet have been interpreted as marine adaptations (Mateus et al. 2009; Tong & Meylan 2013; Cadena 2015). Informative shell and postcranial material is only known from Leyvachelys cipadi. Leyvachelys lacks features found in pelagic marine turtles (cheloniids, dermochelyids and protostegids) as it has an unflattened and unexpanded humerus and metacarpal, a strongly ossified contact between the plastron and carapace, and lacks shell fontanelles (Cadena 2015). Sandownids are therefore thought to have lived in littoral habitats (Cadena 2015).
Extant chelonioids include cheloniids (hard‐shelled sea turtles) and the leatherback sea turtle, Dermochelys coriacea, the only dermochelyid. Molecular phylogenies find chelonioids within Cryptodira, as the sister group to Chelydroidea (Kinosternoidea + Chelydridae; e.g. Crawford et al. 2015; Pereira et al. 2017) in a clade called Americhelydia (Joyce et al. 2013). The number of independent origins of marine adaptation among eucryptodiran lineages depends on the relationships of fossil marine taxa with respect to chelonioids. A summary of phylogenetic hypotheses recovered in previous studies is presented in Figure 1.
Protostegids have frequently been placed on the stem of Dermochelyidae (Hirayama 1994, Kear & Lee 2006; Tong & Meylan 2013; Bardet et al. 2013; Cadena & Parham 2015; Gentry et al. 2018; see Fig. 1E, H). However, Joyce (2007) and some subsequent analyses (Danilov & Parham 2006, 2008; Sterli & de la Fuente 2011, 2013; Anquetin 2012) found protostegids to be basal eucryptodires on the cryptodiran stem (Fig. 1A, B, F, G), or on the turtle stem (Sterli 2010; Sterli & de la Fuente 2011; Fig. 1C). Either position would imply that protostegids evolved marine habits independently of chelonioids, and have typically been found by analysis of the Early Cretaceous Santanachelys as the sole representative of protostegids in a global matrix. When recovered outside Chelonioidea, Santanachelys has been found in a clade with Solnhofia (Danilov & Parham 2006), or Solnhofia and Jurassichelon to the exclusion of plesiochelyids (Joyce 2007; Pérez‐García et al. 2012; Sterli & de la Fuente 2013; Sterli et al. 2013), or a clade including Solnhofia, Jurassichelon and plesiochelyids (Anquetin 2012).
Many previous studies have found the taxa included in Thalassochelydia (sensu Anquetin et al. 2017) to be polyphyletic or paraphyletic (Danilov & Parham 2006, 2008; Joyce 2007; Mateus et al. 2009; Anquetin 2012; Pérez‐García et al. 2012; Sterli & de la Fuente 2013; Sterli et al. 2013; Cadena 2015; Cadena & Parham 2015; see Fig. 1A–F, H, I). This is in part because of the uncertainty that surrounds the positions of Jurassichelon (‘Thalassemys’ moseri in studies previous to the revision provided by Pérez‐García 2015) and Solnhofia, which have been variously grouped with non‐thalassochelydian taxa such as the early protostegid Santanachelys (Danilov & Parham 2006; Joyce 2007; Pérez‐García et al. 2012; Sterli & de la Fuente 2013; Sterli et al. 2013) but also sandownids (e.g. Mateus et al. 2009). Nevertheless, some concept of either one or more clades of Late Jurassic marine turtles has been present in many phylogenetic studies. Three major hypotheses have been presented concerning the positions of these turtles (regardless of their monophyly), as either: (1) stem‐group chelonioids, implying an inclusive clade of marine cryptodires that originated in the Late Jurassic; (2) stem‐group cryptodires, and therefore representing a distinct, independent origin of marine life from that in chelonioids; (3) stem‐group turtles, also representing a distinct origin of marine life. It is clear therefore that thalassochelydians share some traits with chelonioids, and others with stem‐group turtles or stem‐group cryptodires. Indeed, when constituents of Thalassochelydia have been found as stem‐group chelonioids, groups that are otherwise widely regarded as stem‐group cryptodires or stem‐group turtles (xinjiangchelyids, sinemydids; Zhou & Rabi 2015) have sometimes also been found on the stem‐group of chelonioids (Cadena & Parham 2015). However, a sinemydid–chelonioid relationship has also been found in some studies irrespective of the position of thalassochelydians (Brinkman & Wu 1999; Danilov & Parham 2008; Sterli 2010; Pérez‐García 2012). Clearly, resolving the phylogenetic affinities of Thalassochelydia is of great importance for our knowledge of turtle evolution.
Little consensus exists about the relative placement of sandownids (Fig. 1A, E, G, H). Specifically, the relationships of sandownids to ‘eurysternids’, plesiochelyids and chelonioids are unclear. The first reported sandownid, Sandownia harrisi, was originally interpreted as a basal member of Trionychia (softshell turtles; Meylan et al. 2000). However, later studies found little support for this placement (e.g. Joyce 2007) and the patterning of the carapace of Levyachelys is also inconsistent with this hypothesis (Cadena 2015). Sandownia (commonly the only sandownid taxon included in global phylogenetic studies) was tentatively placed on the stem of Cryptodira as a basal eucryptodire by Joyce (2007). Mateus et al. (2009) found sandownids to be sister to Solnhofia in a group called Angolachelonia, which formed part of a marine grade including Jurassichelon, Portlandemys and Plesiochelys on the stem of Cryptodira. Tong & Meylan (2013) and Anquetin et al. (2015) recovered sandownids as the sister‐taxon of chelonioids, and Solnhofia and Jurassichelon as eucryptodires. Finally, Cadena (2015) recovered sandownids as the sister to xinjianchelyids + sinemydids as stem‐group chelonioids, forming a large panchelonioid clade including Jurassichelon and Solnhofia, but excluding plesiochelyids, which were found as stem‐group turtles (Cadena 2015).Material and method
For our character matrix, we used information from three primary sources: Cadena (2015), Zhou & Rabi (2015), and Anquetin et al. (2015). All of these matrices are modified versions of previous studies and can be traced back to Joyce (2007), which represents the first global phylogenetic analysis of Mesozoic turtles. All three source matrices are global in scope but have different foci. Cadena's (2015) matrix is a modified version of the work of Cadena & Parham (2015) and includes character information specific to sandownids. The matrix of Cadena & Parham (2015) is a combination of global matrices (Joyce 2007; Anquetin 2012; Sterli 2008; Sterli & de la Fuente 2013) but importantly includes characters from matrices that were designed to specifically test chelonioid relationships (Hirayama 1994; Hirayama 1998; Kear & Lee 2006; Parham & Pyenson 2010). The Zhou & Rabi (2015) matrix is similarly based on several previous studies, which were focused on the relationships of stem‐group turtles and stem‐group cryptodires (Joyce 2007; Sterli 2008; Sterli & de la Fuente 2013; Rabi et al. 2013, 2014; Zhou et al. 2014). Finally, the analysis of Anquetin et al. (2015) was specifically focused on thalassochelydian relationships. By combining the character lists of these studies, we attempt to capture all morphological variation documented so far among non‐pleurodiran turtles. The 257 characters of Cadena (2015) were reconciled with the slightly different character definitions given in the other two studies, and were further modified by our own observations. This resulted in a phylogenetic data matrix of 345 characters and 80 taxa. In total, 70 characters of Cadena & Parham (2015) were modified (see Coding strategy) and modified versions of 13 characters used by Anquetin (2012), Anquetin et al. (2015), Cadena (2015), Havlik et al. (2014) and Zhou & Rabi (2015) were added. We also added 58 new cranial and mandibular characters. We re‐scored all cranial and mandibular characters from both Cadena & Parham (2015) and other sources, for all taxa in our matrix. Our scorings are based on first hand examination of specimens (44 taxa), examination of CT scans for 59 taxa, photographs of specimens not seen first hand by the authors (shared with SWE by Dr Walter Joyce), and published descriptions (data sources in Table 1). An illustrated character list with discussions of character modifications and additions, and justifications for modified scorings is available in Evers & Benson (2018b, appendix S1).Table 1. Sources for scorings in our character–taxon matrix Taxon Specimen(s) used for character scoring References used for character scoring Personal observation of taxon CT Allaeochelys libyca BSPG 1991 II 130 Havlik et al. (2014) Yes Yes Allopleuron hoffmanni NHMUK R4291; NHMM 000001 Mulder (2003) Yes Yes Annemys sp. IVPP V18106 Brinkman et al. (2013) No Yes Annemys levensis PIN 4636‐4‐2 Sukhanov (2000); Rabi et al. (2014) No No Annemys latiens PIN 4636‐6‐1 Rabi et al. (2014) No No Apalone spinifera emoryi FMNH 22178 No additional references used Yes Yes Araripemys barretoi AMNH 30778 Meylan (1996); Gaffney et al. (2011) Yes Yes Archelon ischyros YPM 3000 Wieland (1896, 1900, 1902) Yes No Argillochelys cuneiceps NHMUK R38955; NHMUK R41636 No additional references used Yes Yes Arundelemys dardeni USNM 497740 Lipka et al. (2006) No Yes Australochelys africanus BP/1/4933 Gaffney & Kitching (1995) Yes Yes Baptemys wyomingensis YPM 374, 3758; DMNH 511 Meylan & Gaffney (1989); Knauss (2014) No No Bouliachelys suteri QMF 31669 Kear & Lee (2006) No Yes Brachyopsemys tingitana AMNH 30001; AMNH 30612 Tong & Meylan (2013) Yes Yes Caretta caretta NHMUK 1918.104.22.168 No additional references used Yes Yes Carettochelys insculpta NHMUK 1903.7.10.1 No additional references used Yes Yes Chelodina oblonga NHMUK 64.12.22 No additional references used Yes Yes Chelodina longicollis a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Chelonia mydas NHMUK 1969.776 No additional references used Yes Yes Chelonoidis sp. SMF 67582 No additional references used No Yes Chelonoidis chilensis a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Chelus fimbriatus NHMUK 22.214.171.124 No additional references used Yes Yes Chelydra serpentina SMF 32846 No additional references used No Yes Chrysemys picta NHMUK 126.96.36.199 No additional references used Yes Yes Chubutemys copelloi MPEF‐PV1236 Gaffney et al. (2007); Sterli et al. (2015) No No Dermatemys mawii SMF 59463 No additional references used No Yes Dermochelys coriacea FMNH 171756; UMZC R3031 No additional references used Yes Yes Desmatochelys lowii KUVP 1200 No additional references used No Yes Desmatochelys padillai FCG‐CBP 01, 13, 15, 39, 40; UCMP 38345, 382456 Cadena & Parham (2015) No No Dracochelys bicuspis IVPP V4075; IVPP V12091 Gaffney & Ye (1992); Brinkman (2001) No No Eileanchelys waldmanni NMS.G.2004.31.15; NMS.G.2004.31.16a‐f Anquetin (2010) Yes Yes Elseya dentata NHMUK 188.8.131.52 No additional references used Yes Yes Emarginachelys cretacea KUVP 23488 Whetstone (1978) No No Emys orbicularis WGJ1987a No additional references used No Yes Eochelone brabantica NHMUK R37213 Casier (1968) Yes Yes Eosphargis breineri FUM‐N‐1450 Nielsen (1959) Yes No Eretmochelys imbricata FMNH 22242 No additional references used Yes Yes Eubaena cephalica DMNH 96004; AMNH 4948, 2602, 2604, 2606; YPM 1785 Gaffney (1972, 1979); Gaffney (1982a, b) No No Geoclemys hamiltoni NHMUK 184.108.40.206 No additional references used Yes Yes Glyptops plicatulus AMNH 336; YPM 1784, 4717, 5821 Gaffney (1979) No No Gopherus polyphemus FMNH 211815 No additional references used Yes Yes Judithemys sukhanovi TMP 87.2.1 Parham & Hutchison (2003) No No Jurassichelon oleronensis PIMUZ AIII 514 Rieppel (1980) Yes Yes Kallokibotion bajazidi NHMUK R4918; NHMUK R4921; NHMUK R4925 Gaffney & Meylan (1992) Yes Yes Kayentachelys aprix TMM 4370‐2, 43653‐1; MCZ 8914‐8917; MNA V1558, V2664 Sterli & Joyce (2007); Gaffney & Jenkins (2010) No Yes Kinosternon suburum hippocrepis FMNH 211711 No additional references used Yes Yes Kinosternon flavescens a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Kirgizemys dmitrievi ZIN PH7/15 Danilov et al. (2006) No No Kirgizemys hoburensis PIN 3334‐4; PIN 3334‐35; PIN 3334‐36 Sukhanov (2000) No No Lepidochelys kempii M009/08 Jones et al. (2012) No Yes Lepidochelys olivacea SMNS 11070 No additional references used Yes Yes Levyachelys cipadi FCG‐CBP‐71; SMU 75377, 72852, 74982, 75327; FWMSH 93B‐17 Vineyard (2009); Cadena (2015) No No Lissemys punctata SMF 74141 No additional references used No Yes Macrochelys temminckii FMNH 22111 No additional references used Yes Yes Meiolania platyceps NHMUK R682; specimens listed in Gaffney (1983) Gaffney (1983) Yes Yes Natator depressus R112123 Jones et al. (2012) No Yes Notochelone costata NHMUK R9590 No additional references used Yes Yes Ocepechelon bouyai OCPDEK/GE516 Bardet et al. (2013) No No Ordosemys sp. IVPP V12092 Brinkman & Wu (1999) No Yes Pelodiscus sinensis IW576‐2 No additional references used No Yes Pelomedusa subrufa SMF 70504 No additional references used Yes Yes Phrynops geoffroanus SMF 45470 No additional references used No Yes Platysternon megacephalum SMF 69684 No additional references used No Yes Plesiochelys planicpes OUMNH J1582 Gaffney (1975a, 1976) Yes Yes Plesiochelys etalloni MNB 435 Gaffney (1975a, 1976) Yes Yes Pleurosternon bullockii UMZC T1041 Evans & Kemp (1975) No Yes Podocnemis unifilis FMNH 45657 No additional references used Yes Yes Podocnemis expansa a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Portlandemys mcdowelli NHMUK R2914 No additional references used Yes Yes Proganochelys quenstedti SMNS 15759, 16980 Gaffney (1990) Yes No Protostega gigas AMNH 1502, 1503; CMNH 1421; FMNH PR2, P27385 Case (1897); Hay (1908) Yes No Puppigerus camperi NHMUK R14375 Moody (1974) Yes Yes Rhinochelys pulchriceps CAMSM B55775, B55783, B55776; NHMUK R43980, R2226, R35197 No additional references used Yes Yes Sandownia harrisi MIWG 3480 Meylan et al. (2000) Yes Yes Sinemys gamera IVPP V9532‐11 Brinkman & Peng (1993) No No Sinemys lens IVPP V9533‐1; IVPP V9533‐3 Brinkman & Peng (1993) No No Solnhofia parsoni TM 4023 Gaffney (1975b) Yes Yes Staurotypus salvinii NHMUK 18220.127.116.11 No additional references used Yes Yes Staurotypus triporcatus a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Sternotherus minor FMNH 211696 Bever (2009) Yes Yes Sternotherus odoratus a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Testudo marginata FMNH 51672 No additional references used Yes Yes Testudo hermanni a a Species indicated by asterisk were used only for postcranial scores. Unknown (specimen number not given in Cadena & Parham 2015) Cadena & Parham (2015) No No Toxochelys sp. AMNH1496, 5118; FMNH UR3; FMNH PR219, PR648 Hay (1896); Nicholls (1988) Yes Yes Xinjiangchelys radiplicatoides IVPP V9539‐1 Brinkman et al. (2013) No Yes Xinjiangchelys wusu PMOL‐SGPA0100‐1; PMOL‐SGPA0100‐3 Rabi et al. (2013) No No
Phylogenetic analyses of morphology are used to infer relationships from a set of comparative anatomical observations. The concept of homology is central to the delimitation of these observations as characters and character states. Homology is the hypothesis that similar attributes shared by different species are equivalent to one another due to common ancestry, and therefore reflect their phylogenetic relationships (Platnick 1979; Eldredge & Cracraft 1980; de Pinna 1991; see Patterson (1982) for a disambiguation and extensive discussion of homology). Hypotheses of homology are established based on topographic and ontogenetic correspondence and on compositional similarity of traits (Patterson 1982; Rieppel 1988; de Pinna 1991; Hawkins et al. 1997). These initial (‘primary’; de Pinna 1991) hypotheses of homology are embodied by the characters and character states, and are tested against one another by means of congruence in parsimony analysis, which maximizes the number of initial homology propositions that are upheld as true homology rather than the result of convergent evolution (homoplasy; Patterson 1982; de Pinna 1991).
Character construction therefore represents the proposition of initial hypotheses of homology based on observations of similarity. Character states are different forms that a homologous trait (i.e. the character) can take among organisms, and are equivalent transformations of one another on a single hierarchical level (the level of the character) (Platnick 1979; de Pinna 1991; Hawkins et al. 1997). Characters and character states therefore form a hierarchical framework of homology propositions. For example, a specific site in the aligned nucleotide sequences of several organisms is hypothesized to be comparable on the character level, and the (four or five) nucleobases represent possible variation of this character on the character state level (and could therefore not represent separate characters themselves) (Pleijel 1995). Construction of morphological characters is potentially more subjective. Nevertheless, we have taken various steps to ensure that our cladistics characters for turtles, both new, and modified from previous analyses, reflect homology (described below).
Character states should also be independent of each other (e.g. Pimental & Riggins 1987; Strong & Lipscomb 1999). Non‐independence of character states is problematic because it results in a single observation of similarity being coded twice, and therefore the character state is arbitrarily given a greater weight than others (Wilkinson 1995; Strong & Lipscomb 1999). Logical dependence between characters exists when the score of a taxon for one character directly affects the scoring of the same taxon in another character (e.g. coding the absence and zero size of a feature; Wilkinson 1995), and this can be readily avoided. Biological dependence is a hypothesis that character states of different characters are non‐independent due to functional or developmental linkage (Wilkinson 1995). Information on the underlying biological cause for such a linkage if often not available, which makes is hard to fully avoid biological independence in character construction.
Many morphological characters used in previous studies of turtle phylogeny combine complex observations across multiple hierarchical levels of similarity, or lump together independently varying character states. We re‐coded characters so that independently varying aspects of morphological variation are coded in separate characters. For example, character 10 of Cadena & Parham (2015) was defined as:
In this character definition, the absence of a jugal–squamosal character is assumed to be linked to the presence of a postorbital–quadratojugal contact. The character includes the assumption that a postorbital–quadratojugal character must be present when a jugal–squamosal contact is absent. However, these contacts vary independently from one another, as taxa exist (trionychids) in which a postorbital–quadratojugal contact is absent, but a jugal–squamosal contact is also absent. The approach taken here is to break up this character into two separate characters, which each code for one of the contacts (our chs 25 and 42).
We also re‐coded characters so that observations across multiple hierarchical levels of similarity are coded in separate characters. For example, we modified character 60 of Cadena & Parham (2015), which was phrased as:
The comparative anatomical observations underlying this and similar characters include both the absence of a certain feature, and variation in the shape of that feature when present (the ‘no tail; red tail; blue tail’ problem; Maddison 1993; Smith 1994; Hawkins et al. 1997; Brazeau 2011). Coding these observations into a single character, as done in most turtle studies (e.g. Joyce 2007; Cadena & Parham 2015; but see Anquetin 2012) assumes that the condition of having no epipterygoid is on the same hierarchical level as the observed shape conditions of taxa with epipterygoids. This disregards the homology implied by the presence of an epipterygoid in various taxa, irrespective of its of shape (Hawkins et al. 1997), resulting in loss of information.
To reflect the hierarchical levels of similarity of these observations of the epipterygoid, and other characters in our analysis, we used a hierarchical coding strategy. For the above example, this reformulation results in two separate characters. One character codes for the presence versus absence of the feature (e.g. epipterygoid; our ch. 87), and the second codes for the various shapes that the feature can take (e.g. epipterygoid shape; our ch. 88) (Hawkins et al. 1997; Brazeau 2011; see Anquetin 2012 for a turtle study using the same approach). Logical dependence of the character states of the second character on the first is avoided by scoring the second character as inapplicable (‘–’) when the first character is scored as ‘absent’. Inapplicability does not introduce logical dependency (contra Strong & Lipscomb 1999) because it does not represent a separate character state, and transitions to ‘inapplicable’ do not count towards the length of a cladogram. However, inapplicable scores can be problematic because inapplicability is treated the same as missing data in software implementations of parsimony analysis (e.g. Platnick et al. 1991; Strong & Lipscomb 1999; Brazeau et al. 2017). This can introduce illogical character state reconstructions during the optimization process (e.g. Platnick et al. 1991; Maddison 1993). This problem relates to computational issues that may be solved in future generations of software (e.g. Brazeau et al. 2017), and problems with inapplicable character states are herein taken to be less problematic than the homology issues of compound characters discussed above (Strong & Lipscomb 1999; Hawkins et al. 1997).
Some of our characters appear superficially to be hierarchical compound characters (as in Cadena & Parham 2015, ch. 60; above), because they include an absence state as well as several other non‐absence states. However, these characters are measurements such as the size of a structure, for which absence equates to zero. It is therefore appropriate to treat their character states as homologous with each other at the same hierarchical level. For example, our character 7 (ch. 7 of Cadena & Parham 2015):
Our approach also differs from some recent analyses of turtles (e.g. Anquetin 2012) that exclusively used binary characters. Instead, we coded instances for which multiple conditions are observed for a character as multistate characters, reflecting the hypothesis that these alternative conditions represent transformations of a single underlying feature. For example, our character 297 (identical to ch. 210 of Cadena & Parham (2015)):
The alternative approach of only using binary characters (e.g. Anquetin (2012) for turtles) requires the construction of a series of characters, or ignoring observations to artificially create binary characters, or lumping a set of distinct character states into a single character state (as done in the above example by Anquetin (2012): ch. 160, in which the conditions of procoely and opisthocoely are lumped into a single character state). Anquetin (2012) justified the usage of binary characters by stating that this approach minimizes the amount of ‘a priori assumptions about homology’ (Anquetin 2012, p. 5). However, this avoidance of homology proposition misapplies the similarity criterion used to establish primary hypotheses of homology, which are always a priori hypotheses (de Pinna 1991; Hawkins et al. 1997). Instead of avoiding assumptions of homology, the approach of Anquetin (2012) generates unexpected hypotheses of homology (e.g. that procoely and opisthocoely are interchangeable, and homologous with each other on a low hierarchical level).
Our operational taxonomic units (OTUs) were chosen specifically to test the phylogenetic relationships of non‐pleurodiran marine turtles, and we preferentially used taxa for which we had CT data. Our matrix includes many chelonioids, thalassochelydians, protostegids and sandownids (Table 1). To test the placement of these groups in a global framework, we also included a thorough sample of stem‐group turtles, including Triassic and Early Jurassic species, as well as paracryptodires and meiolaniforms. We further included a range of xinjiangchelyids, sinemydids and macrobaenids, which have been hypothesized to be stem‐group cryptodires (e.g. Zhou & Rabi 2015). We sampled extant representatives of modern clades including pleurodires, and all families of turtles. We included early fossil representatives of extant families when CT data was available to us or when sufficiently detailed anatomical descriptions were available in the literature. Of particular importance, two fossil chelydroids, Emarginachelys cretacea and Baptemys wyomingensis, were included because chelydroids (kinosternoids + chelydrids) are the extant sister‐group to chelonioids (Crawford et al. 2015) and fossil representatives of this group can thus influence character optimizations for the total group of Americhelydia (chelydroids + chelonioids).
Most of our OTUs represent modern or fossil taxa on the species level, but some OTUs are supraspecific: the extant taxa Chelodina, Chelonoidis, Kinosternon, Podocnemis, Staurotypus, Sternotherus and Testudo. This was done because our CT scans, which were used to re‐score the cranial and mandibular characters, belonged to different species from those used by Cadena & Parham (2015) (Table 1), and we retained their postcranial characters. We chose to score a supraspecific OTU for Toxochelys because this allowed inclusion of data from specimens that have been assigned to different species, and thus score a more complete OTU. Species assignments regarding specimens of Toxochelys are currently uncertain (Zangerl 1953; Nicholls 1988; Brinkman et al. 2006), particularly because the holotype specimens of valid species are relatively incomplete and lack cranial material. Pending a taxonomic revision of Toxochelys material, we consider it best to refer most Toxochelys material to Toxochelys sp., as done by some other authors (e.g. Brinkman et al. 2006).
The protostegid Rhinochelys pulchriceps was scored primarily from CT scans of the holotype specimen CAMSM B55775. However, we also used data from CT scans of other specimens, which have been referred to different species of Rhinochelys (Collins 1970; see Table 1 for specimens used). These added information on the mandible (R. cantabrigiensis: CAMSM B55783; R. elegans: CAMSM B55776). It is likely that all British specimens of Rhinochelys represent a single species (SWE, unpublished data), and we therefore consider all material in Collins (1970) to be Rhinochelys pulchriceps.
We used high‐resolution X‐ray computed‐tomography (CT) data for as many taxa as possible (summarized in Table 1). To support our anatomical observations and opinions stated throughout this work, we deposited several CT datasets and 3D models generated through manual segmentation in the software Mimics (versions 16.0–19.0; http://biomedical.materialise.com/mimics) in MorphoSource (Evers & Benson 2018a). The data represent a sample of fossil and extant turtle specimens that have been extensively used in character construction and illustration of characters (see Evers & Benson 2018b, appendix S1). These are: Apalone spinifera emroyi (FMNH 222178), Dermochelys coriacea (UMZC R3031), Elseya dentata (NHMUK 18.104.22.168), Gopherus polyphemus (FMNH 211815), Lepidochelys olivacea (SMNS 11070), Phrynops geoffroanus (SMF 45470), Plesiochelys planiceps (OUMNH J1582), Argillochelys cuneiceps (NHMUK R38955), Sandownia harrisi (MIWG 3480), Solnhofia parsoni (TM 4023), Sternotherus minor (FMNH 211696) and Rhinochelys pulchriceps (CAMSM B55783; referred to Rhinochelys cantabrigiensis by Collins (1970), but see Taxon Sampling, above). Because scanning parameters varied between all scans, details are given in the online repository with the data (Evers & Benson 2018a) and are not summarized here.
To illustrate the structure of our dataset, we produced heatmaps of similarity matrices calculated from our character–taxon matrix in R (R Core Team 2016). Polymorphisms and missing data (‘?’) were treated as inapplicable data. Similarity between two taxa was calculated as the number of identical scoring matches between these taxa divided by the number of comparable scores between them (e.g. Sneath & Sokal 1973; Foote 1994; Wagner 1997; see Benson & Druckenmiller 2014 for a similar code). The resulting values are represented in a symmetric similarity matrix. Similarity matrices were calculated for the total dataset, and partitions of that dataset representing cranial and mandibular characters, shell characters, limb characters and axial + girdle characters. For the anatomical partitions of the total dataset, taxa with no anatomical information for the respective partition, as well as taxa with 90% or more missing data were excluded. Each similarity matrix was coloured by assigning a spectrum of colours to the similarity values of each matrix using the package gclus (Hurley 2012). The R code for calculating similarity and producing the heatmaps is available in Evers & Benson (2018b).
Tree searches were performed in TNT 1.5 for Windows (Goloboff et al. 2008; Goloboff & Catalano 2016). For all analyses, we used a molecular backbone constraint following the topology of Pereira et al. (2017) for extant taxa. All fossil taxa were left unconstrained and were thus allowed to fall anywhere within the constrained topology of extant taxa. Proganochelys quenstedti was set as the outgroup. In TNT, new technology algorithms were used with default settings, and tree drifting (Goloboff 1999) and parsimony rachet (Nixon 1999) enabled. The initial level of the driven search was set to 30, and the number of times the minimum tree length should be obtained was set to 30. This procedure does not require specifying a number of replicates to be performed (Goloboff 1999; Giribet 2007). The most parsimonious trees (MPTs) of this analysis were then subjected to a final round of tree bisection and reconnection (TBR). The resulting MPTs were used to construct a strict consensus tree.
Characters were treated as unordered and equally weighted in our initial analysis. We also executed a second run in which several characters were ordered, for comparison (chs 7, 14, 18, 34, 44, 67, 76, 79, 90, 93, 94, 103, 107, 123, 130, 131, 138, 142, 147, 205, 210, 217, 248, 253, 292, 305, 325, 339, 340, 344). Ordering character states represent a priori hypotheses that transitions between character states only occur in a specific sequence (e.g. Wilkinson 1992, 1995). However, prior knowledge about the evolutionary sequence of character state transitions is often missing or otherwise not substantiated by evidence. Therefore, we only ordered multistate characters in which one character state was directly intermediate in form, size, or number of two other states (for instance ch. 340: size of ulnare vs intermedium: 0 = ulnare smaller than intermedium; 1 = ulnare nearly as large as intermedium; 2 = ulnare much larger than intermedium). If clear intermediates are not evident, the states were left unordered (for instance ch. 260: medial contact of extragulars: 0 = absent; 1 = contacting each other anterior to gulars; 2 = contacting each other posterior to gulars).
Bremer support was calculated in TNT, using the absolute Bremer support setting and TBR branch swapping on existing trees to generate suboptimal trees. Character optimization was performed in PAUP* for Macintosh (Swofford 2002) because TNT only returns unambiguous synapomorphies (i.e. those in which ACCTRAN and DELTRAN agree in determining a character state change) whereas the optimization criterion can be specified in PAUP*. The optimization was computed on a fully resolved tree. This tree was chosen from the MPTs on the basis of high congruence with a 50% majority rule consensus tree. The most important differences between the tree selected for optimization and our consensus topology are that paracryptodires are monophyletic and that the species of Sinemys form a clade that is sister group to all remaining sinemydids (see Evers & Benson 2018b, appendix 2, fig. S2.1). The tree topology chosen for the optimization, as well as unambiguous, ACCTRAN, and DELTRAN optimizations for all characters as well as all nodes are given in Evers & Benson (2018b, appendices S1–2).
To illustrate implications of our results for the age of crown‐group chelonioids (see Discussion, below), we produced a time‐scaled tree using age‐ranges of taxa derived from the literature and the PalaeoDB (https://paleobiodb.org), summarized in Table 2. Commands from the strap (Bell & Lloyd 2014) and paleotree (Bapst 2012) packages in R were used for time‐scaling and visualization. We arbitrarily used a minimum branch length argument of 1 myr for zero‐branch lengths in the timePaleoPhy command of the paleotree package (Bapst 2012). Because some lineages of turtles have older fossil representatives than the oldest fossils for those groups included in our study, we included minimum constraints for three nodes of our time scaled tree. First, we used the top of the Oxfordian (157.3 Ma) as a minimum constraint for Pleurodira based on Caribemys oxfordiensis (de la Fuente & Iturralde‐Vinent 2001; Joyce et al. 2013). Secondly, we used the base of the Cretaceous (145.0 Ma) as a minimum constraint for Cryptodira based on the total‐group trionychian Sinaspideretes wimani. Although the type locality of Sinaspideretes is not exactly known (Tong et al. 2014) it is likely that the material as well as referred material is from the Shangshaximiao Formation (Danilov & Parham 2006; Tong et al. 2014), which is probably of Late Jurassic but possibly even of Middle Jurassic age (Xing et al. 2013). Using the base of the Cretaceous as a minimum age is thus a conservative constraint, following Joyce et al. (2013). Lastly, again following Joyce et al. (2013), we use the top of the Campanian (72.1 Ma) as a minimum constraint for Chelydroidea based on a peripheral fragment that can be unambiguously identified as belonging to the total‐group of Chelydridae, which was described by Brinkman & Rodriguez de la Rosa (2006).Table 2. Stratigraphic ranges for taxa used for our time‐calibrated tree (Ma) Taxon First appaearance datum (FAD) Last appearance datum (LAD) Source Allopleuron hofmanni 72.1 66.0 Janssen et al. (2011) Annemys latiens 163.5 145.5 Rabi et al. (2010) Annemys levensis 157.3 145.5 Rabi et al. (2010) Annemys sp. 167.7 145.0 PalaeoDB Araripemys barretoi 112.6 109.0 PalaeoDB Archelon ischyros 83.6 72.1 Hirayama (1997) Argillochelys cuneiceps 56.0 47.8 Weems & Brown (2017) Arundelemys dardeni 122.46 112.6 PalaeoDB Australochelys africanus 201.6 189.6 PalaeoDB Baptemys wyomingensis 55.8 40.4 PalaeoDB Bouliachelys suteri 105.3 99.7 PalaeoDB Brachyopsemys tingitana 66.043 61.7 PalaeoDB Chubutemys copelloi 125.45 112.6 PalaeoDB Desmatochelys lowii 93.9 89.8 Hirayama (1997) Desmatochelys padillai 125.0 120.0 Cadena & Parham (2015) Dracochelys biscuspis 125.0 100.5 Rabi et al. (2010) Eileanchelys waldmanni 168.3 166.1 Joyce et al. (2016b) Eubaena cephalica 70.6 66.043 PalaeoDB Emarginachelys cretacea 70.6 66.043 PalaeoDB Eochelone brabantica 47.8 41.2 Weems & Brown (2017) Eosphargis breineri 56.0 47.8 Nielsen (1959) Glyptops plicatulus 150.8 145.5 PalaeoDB Judithemys sukhanovi 84.9 70.6 PalaeoDB Jurassichelon oleronensis 152.1 145.0 Rieppel (1980); Anquetin et al. (2017) Kallokibotion bajazidi 72.1 66.0 Joyce et al. (2016b) Kayentachelys aprix 199.3 182.7 Joyce et al. (2016b) Kirgizemys dmitrievi 130.0 112.6 PalaeoDB Kirgizemys hoburensis 125.0 100.5 Rabi et al. (2010) Leyvachelys cipadi 130.0 109.0 PalaeoDB Notochelone costata 109.0 99.7 PalaeoDB Ocepechelon bouyai 70.6 66.043 PalaeoDB Ordosemys sp. 129.4 113.0 Rabi et al. (2010) Plesiochelys etalloni 157.3 150.0 Anquetin et al. (2017) Plesiochelys planiceps 152.1 145.0 Anquetin et al. (2017) Pleurosternon bullockii 145.2 140.2 PalaeoDB Portlandemys mcdowelli 152.1 145.0 Anquetin et al. (2017) Proganochelys quenstedti 208.5 201.3 Joyce et al. (2016b) Protostega gigas 85.8 70.6 PalaeoDB Puppigerus camperi 56.0 41.2 Weems & Brown (2017) Rhinochelys pulchriceps 105.3 102.0 PalaeoDB for FAD; LAD following Collins (1970) Sandownia harrisi 125.45 122.46 PalaeoDB Santanachelys gaffneyi 112.6 109.0 PalaeoDB Sinemys gamera 129.4 100.5 Rabi et al. (2010) Sinemys lens 163.5 145.0 Rabi et al. (2010) Solnhofia parsoni 155.7 145.5 PalaeoDB; Joyce (2000) Toxochelys latiremis 85.8 70.6 PalaeoDB; Weems & Brown (2017) Xinjiangchelys radiplicatoides 168.3 152.1 Rabi et al. (2010) Xinjiangchelys wusu 163.5 152.1 PalaeoDB
To test if our phylogenetic results were influenced by the inclusion of characters that might be functionally linked to a marine lifestyle, we performed an additional analysis in which characters that were identified as being indicative of a marine lifestyle were deleted. Furthermore, to test if our phylogenetic results (specifically, the recovery of protostegids being crown‐group chelonioids, see Results below) were driven by the inclusion of advanced taxa with a highly specialized body plan with clear adaptations to pelagic life, as suggested by some authors (e.g. Cadena & Parham 2015), we performed a series of analyses in which only certain protostegids with the most plesiomorphic characters were included in the analyses. In the first of these ‘least specialized taxa analyses’, we only kept Santanachelys gaffneyi as the only representative of protostegids, as done in all studies that previously found protostegids outside Chelonioidea (e.g. Joyce 2007; Danilov & Parham 2008; Anquetin 2012; Sterli & de la Fuente 2013). In our second analysis (least specialized taxa analysis 2), we additionally kept Rhinochelys pulchriceps, for which we had the most detailed cranial information. In a third analysis (least specialized taxa analysis 3), we kept all protostegids but Archelon ischyros and Protostega gigas, which are commonly described as ‘advanced protostegids’ (e.g. Kear & Lee 2006).
To test if our topology was significantly different in tree length compared to alternative hypotheses regarding the placement of key taxa, we used Templeton's non‐parametric test (Templeton 1983) in PAUP* for Macintosh (Swofford 2002). Templeton's test uses the differences in counts of character state transitions for each character implied by a pair of trees. Resulting differences are sorted in ascending order and fractional rank scores are assigned to them. Rank scores for characters that have fewer transitions in the suboptimal tree are summed to produce a test statistic, which is subjected to a Wilcoxon's signed rank test. The default for PAUP* is a two‐tailed test (Goldman et al. 2000). However, because we use Templeton's test with one tree being known to be optimal (the null hypothesis is that constrained topologies fit the data as well as the optimal, i.e. shortest, tree) a one‐tailed test is appropriate (Templeton 1983; Goldman et al. 2000; Hipp et al. 2004). Although p‐values of one‐tailed tests are less conservative, their use has been advocated because they are generally close to the exact probability values for this test (Felsenstein 1985; Lee 2000) and p‐values reported herein were corrected accordingly (see Goldman et al. 2000). Alternative hypotheses were chosen based on phylogenetic results presented in previous studies. Our alternative hypotheses test the position of plesiochelyids, thalassochelydians, sandownids, xinjiangchelyids, sinemydids, protostegids as stem‐group cryptodires and stem‐group chelonioids, respectively, and the position of protostegids as stem‐group turtles. The alternative topologies were recovered by running parsimony analyses including one OTU relevant to each hypothesis into the molecular backbone constraint, while all other fossil OTUs were kept as floaters. For hypotheses relating to species‐rich groups or groups that have not consistently been found to be monophyletic among previous studies, such as sinemydids or thalassochelydians, several constraints using different OTUs were used. Because Templeton's test uses character changes across a tree in a pairwise comparison, individual trees had to be selected from the available MPTs of the original and constraint analyses. To do this, we computed symmetric differences (Robinson & Foulds 1981) between all MPTs from each constraint analysis and all MPTs of our original analysis using the command treedist in PAUP*, which returns a pairwise symmetric differences matrix. The least and most symmetric tree pairs between original and constraint analyses were selected from the matrix for comparison. If several tree pairs matched the least or most symmetry criterion, we randomly chose a tree pair from the symmetric difference matrix for the Templeton's tests (the procedure, including PAUP* and R code, are provided in Evers & Benson (2018b) along with all MPTs and consensus trees generated for alternative hypotheses).Results
Similarity heatmaps show high or low similarity of character states. Most clades show relatively low between‐group similarity, and relatively high within‐group similarity (Fig. 2), congruent with our phylogenetic topology. Relatively high between‐group similarity of some clades that are not close relatives of one another (according to our phylogenetic results) provide evidence of homoplasy, and possibly indicate convergent evolution.Figure 2 Open in figure viewerPowerPoint Heatmap of symmetric pairwise‐taxon similarity matrix using our full character dataset (n = 345). The phylogenetic tree to the left is identical to our strict consensus tree using unordered character data. Dotted lines delimit turtle subclades for readability. Abbreviations: AC, Angolachelonia; BS, basal stem‐group turtles; CH, Cheloniidae; CY, Chelydroidea; D, Dermochelyidae; M, Meiolaniformes; PC, Paracryptodira; PL, Pleurodira; PR, Protostegidae; SM; Sinemydidae/Macrobaenidae; T, Toxochelys sp.; TE, Testudinoidea; TR, Trionychia, XI, Xinjiangchelyidae. Colour online.
Some of the highest between‐group similarity is seen between protostegids on one hand, and sinemydids, xinjiangchelyids and angolachelonians (i.e. thalassochelydians + sandownids; details are given below) on the other hand (Fig. 2). This pattern has been noted based on qualitative comparisons before (Cadena & Parham 2015), and is according to our matrix driven predominantly by cranial and, to a lesser extent, axial + girdle characters (Fig. 3A, C). Our phylogenetic results strongly support the hypothesis that protostegids are crown‐group chelonioids, deeply nested within Cryptodira. This pattern of similarity therefore indicates a relatively high amount of convergence of the protostegid skull morphology with that of angolachelonians, sinemydids and xinjiangchelyids. In accordance with our topology, protostegid skull morphology is most similar to the skull morphology of cheloniids. However, unlike in the axial + girdle or shell partitions, cranial similarity between protostegids and cheloniids never exceeds moderate values. Paired with the moderate similarity of cranial morphology of protostegids with non‐chelonioid groups, the relatively strong differences of protostegid skulls to cheloniid skulls reveal a high amount of potential character conflict. This might explain the finding of protostegids outside Chelonioidea in some previous studies (e.g. Joyce 2007; Anquetin 2012). Furthermore, the character similarity between sinemydids, xinjiangchelyids, and angolachelonians can be used as an explanation for the unstable positions of these groups among previous phylogenetic analyses (e.g. Rabi et al. 2013; Cadena & Parham 2015; Zhou & Rabi 2015; see Discussion, below).Figure 3 Open in figure viewerPowerPoint Heatmaps of symmetric pairwise‐taxon similarity matrices of subsets of our characters data. A, cranial character data (n = 185). B, shell character data (n = 87). C, axial and girdle character data (n = 50). D, limb character data (n = 23). Note that NA values result from comparisons of taxa with non‐overlapping character preservation. Abbreviations: AC, Angolachelonia; BS, basal stem‐group turtles; CH, Cheloniidae; CY, Chelydroidea; D, Dermochelyidae; M, Meiolaniformes; PC, Paracryptodira; PL, Pleurodira; PR, Protostegidae; SM; Sinemydidae/Macrobaenidae; T, Toxochelys sp.; TE, Testudinoidea; TR, Trionychia, XI, Xinjiangchelyidae. Colour online.
Although angolachelonians are particularly similar to protostegids, the similarity of angolachelonians to chelonioids in general is high. This pattern is seen across all data partitions, and is most evident in the cranial data. However, our data partitions also show that, whereas angolachelonian skulls share more identical scorings with protostegids than with cheloniids, the shells of angolachelonians are more similar to cheloniids than to those of protostegids. High overall similarity between chelonioids and angolachelonians can possibly be explained by their marine lifestyle. Relatively high cranial similarity between Angolachelonia and Chelonioidea indicates that character convergence is more dominant in the cranium of these marine groups, than in other parts of the body.
Chelonioids (including protostegids) show high within‐group similarity for all anatomical partitions, and relatively low similarity to other groups (Fig. 3). This is particularly evident for limb morphology (Fig. 3D). The same pattern, albeit weaker, is also seen in shell, and axial + girdle morphology. This indicates that chelonioids have a specific set of shell, postcranial, and especially limb characters that differs relatively strongly to the characters of other groups, but that these characters are consistently present among members of Chelonioidea. For skull characters, low similarity values to non‐chelonioid groups are only observed in cheloniids (see discussion of protostegids above). This indicates that within Chelonioidea, the cheloniid skull has a high number of derived character states. Dermochelyoids show a strong dissimilarity to all other groups (but moderate to high similarity to cheloniids) in the shell partition, indicating a strongly derived shell morphology. Although within‐group similarity in chelonioids is generally high, cheloniids and dermochelyoids can be distinguished in the cranial and limb partitions, indicating that these parts of the body are less similar than the shell or axial + girdle skeleton.
Relatively high between‐group similarity is present among xinjiangchelyids, sinemydids and paracryptodires, which is particularly clear in the cranial and shell data, but also seen in the unpartitioned dataset. This is in accordance with our phylogenetic results, which find these groups relatively closely related to one another on the stem‐lineage of turtles. Moderate similarity is seen between testudinoids, sinemydids and xinjiangchelyids, possibly explaining why the latter groups are sometimes found as stem‐group cryptodires (e.g. Pérez‐García et al. 2012; Sterli et al. 2013; Zhou & Rabi 2015).
The similarity of pleurodires to other turtles is lower in the cranial and shell partitions than in the axial + girdle or limb partitions. Therefore, the limbs, girdles and axial elements of pleurodires are similar to those of cryptodires, whereas their skulls and shells are highly different. This might be explained by constraints imposed onto the limbs and postcranium by the presence of the shell in all turtle groups, and apparent absence of these constraints on the shell itself and the cranium.
Indeed, the limbs and axial + girdle partition shows relatively high similarity between almost all groups (Fig. 3C). Exceptions to the general pattern include chelonioid limbs, which are modified to flippers and thus dissimilar to those of all other turtles (Fig. 3D), and stem‐group turtles including meiolaniforms and paracryptodires. These show relatively low similarity (i.e. are dissimilar) to all other groups, especially among early stem‐group turtles. This indicates that the axial, girdle and limb morphology underwent substantial transformation on the turtle stem‐lineage, but then was relatively conserved within the turtle crown‐group. Finally, angolachelonians and sinemydids show higher axial + girdle and cranial similarity to cryptodires than to pleurodires, which could possibly explain their inferred positions as stem‐group cryptodires in some studies (e.g. Zhou & Rabi 2015).
Parsimony analysis of the unordered dataset in TNT resulted in 12 most parsimonious trees (MPTs) 1532 steps long. Subsequent TBR branch swapping resulted in recovery of 12 MPTs in total. Zero‐branch lengths are collapsed during the construction of a strict consensus tree in TNT. In several cases (Trionychidae, Chelinae), resulting polytomies in our strict consensus tree can actually be resolved on the basis of the molecular backbone constraint, and nodes representing these clades have been added back in to the respective figures (Fig. 4).Figure 4 Open in figure viewerPowerPoint Strict consensus trees of our phylogenetic analysis. A, strict consensus tree of 12 MPTs from analysing our data treating the characters as unordered. B, strict consensus tree of 195 MPTs treating characters as ordered. Numbers above nodes are Bremer values.
In the following, results from our unordered analysis are presented. Differences in topology found in the ordered analysis are described in the section below, and shown in Figure 4. Key results from our unordered phylogenetic analysis are: (1) the recovery of a previously unknown clade, Angolachelonia, comprising sandownids + thalassochelydians, which is placed as the immediate sister group to crown‐group turtles; (2) the recovery of a monophyletic Protostegidae as the sister to Dermochelyidae; (3) the recovery of all sinemydids, macrobaenids, and xinjiangchelyids as stem‐group turtles. Our results imply two independent and monophyletic groups of marine turtles outside Pleurodira: Angolachelonia and Chelonioidea. This shows that marine ecologies have evolved three times within non‐pleurodiran turtles, including Odontochelys.
Angolachelonia includes two monophyletic groups that have been previously recognized: Sandownidae and Thalassochelydia. The branch support for Angolachelonia is moderate (Bremer support = 3). Angolachelonia is supported by eight unambiguous synapomorphies (all cranial and mandibular; see Figs 5, 6; Table 3), of which none are unique. Within Angolachelonia, sandownids and plesiochelyids have high branch support values (Bremer support = 4), whereas Thalassochelydia (i.e. Plesiochelyidae + Solnhofia in the context of our taxon sampling) has moderate support (Bremer support = 2). Thalassochelydians share eight unambiguous synapomorphies (four cranial and mandibular; see Fig. 7; four postcranial, one of which is unique (ch. 278.0); Table 3); sandownids are united by four unambiguous cranial synapomorphies (Fig. 8; Table 3), one of which is unique (ch. 108.1). The sister‐group relationship of Angolachelonia and crown‐group turtles is well supported (Bremer support = 4).Figure 5 Open in figure viewerPowerPoint Cranial synapomorphies of Angolachelonia illustrated by renderings of 3D models generated using CT data. A, cranium of Solnhofia parsoni (TM 4023) in dorsal view showing the extend of the dermal skull roof in the temporal region, obliterating the foramen stapedio‐temporale in dorsal view (ch. 18.0). B, cranium of Sandownia harrisi (MIWG 3480) in dorsal view, showing the same features as in A. C, cranium of Solnhofia parsoni (TM 4023) in ventral view, showing the posterior direction of the articular process (ch. 84.1), the long interpterygoid contact (ch. 94.0), and the contact of the pterygoid with the mandibular articular surface of the quadrate (ch. 103.1). D, cranium of Plesiochelys planiceps (OUMNH J1582) in ventral view, showing the same features as in C. E, cranium of Solnhofia parsoni (TM 4023) in posteroventral view, showing the infolding ridge of the quadrate (ch. 83.1). F, cranium of Brachyopsemys tingitana (AMNH FARB 30612) in posteroventral view, showing the same features as in E. Abbreviations: apc, articular process of cranium; fst, foramen stapedio‐temporale; iqr, infolding ridge of quadrate; pt, pterygoid; q, quadrate. Scale bars represent: 10 mm (A–C, E); 20 mm (D, F). Colour online. Figure 6 Open in figure viewerPowerPoint Mandibular synapomorphies of Angolachelonia illustrated by renderings of 3D models generated using CT data. A, right mandibular ramus of Solnhofia parsoni (TM 4023) in lateral view, showing the coronoid notch (ch. 181.1) and the tall and pointed coronoid process (ch. 184.1). B, right mandibular ramus of Solnhofia parsoni (TM 4023) in medial view, showing the foramen in the coronoid (ch. 182.1). C, right mandibular ramus of Sandownia harrisi (MIWG 3480) in lateral view, showing the same features as in A. D, right mandibular ramus of Sandownia harrisi (MIWG 3480) in medial view, showing the same features as in B. Note that the coronoid has been shaded in all images. Abbreviations: cor f, foramen in coronoid; cor n, coronoid notch; cor p, coronoid process. Scale bars represent 10 mm. Colour online. Table 3. Synapomorphies for taxa discussed in the main text Taxon Unambiguous synapomorhies Sum Chelonioidea (total‐group) 35.1, 39.1, 58.1, 69.0, 94.0, 105.1, 132.2, 139.2, 142.1, 144.1, 163.1, 210.2, 235.0, 242.2, 255.2, 291.1, 295.0, 333.1, 334.1, 338.1, 342.1 21 Chelonioidea (crown‐group) 15.0, 93.2, 104.0, 306.1, 307.1, 337.1, 344.1 7 Cheloniidae (total‐group) 44.1, 68.1, 109.1, 119.1, 176.1 5 Dermochelyoidea 27.0, 161.1, 237.1, 340.2 4 Dermochelyidae 16.1, 53.1, 96.0, 110.0, 115.0, 149.1 6 Protostegidae 4.0, 62.1, 103.1, 236.1, 291.0, 328.1, 329.1, 335.1 8 Angolachelonia 18.0, 83.1, 84.1, 94.0, 103.1, 181.1, 182.1, 184.1 8 Sandownidae 34.0, 57.1, 68.1, 108.1 4 Thalassochelydia 81.1, 113.1, 142.1, 185.0, 210.2, 211.1, 224.0, 278.0 8 Sinemydidae/Macrobaenidae 113.1, 134.1, 242.2, 243.1 4 Xinjiangchelyidae 38.1, 91.0, 125.1, 203.1, 257.1, 270.1 6
Chelonioidea is a monophyletic group comprised of two major subgroups, Dermochelyoidea and Cheloniidae. Toxochelys is found as the only member of the chelonioid stem‐group. Within the total‐group of Cheloniidae, all extant cheloniids form a clade, and all fossil taxa are found to be stem‐group cheloniids forming a paraphyletic grade as successive sister‐taxa to the crown. Eochelone is found as the earliest‐diverging cheloniid in our taxon sample across all trees. The total‐group of Cheloniidae has a Bremer support of 2 and is supported by five unambiguous synapomorphies (Table 3), all of which are cranial, and none of which are unique. Dermochelyoidea includes the extant leatherback turtle Dermochelys coriacea and its stem‐group, including Eosphargis breineri and protostegids. Among the stem‐group of Dermochelys, Eosphargis is found as the closest relative of Dermochelys. Different authors have used different taxonomic terminology to refer to Dermochelys and closely related taxa. The name Dermochelyidae has most frequently been used to describe Dermochelys and taxa on its stem‐lineage to the exclusion of protostegids (e.g. Hirayama 1994, 1998; Kear & Lee 2006). This has been formalized in a phylogenetic definition by Joyce et al. (2004). We use Dermochelyidae in that sense. Dermochelyidae is herein supported by a Bremer support of 4, and by six unambiguous cranial synapomorphies (Table 3), none of which are unique. The total‐group of Dermochelys (i.e. dermochelyids + protostegids) has also received various names (Hirayama 1998; Joyce et al. 2004). Here, we use the name Dermochelyoidea for this group (as in Hirayama 1998; Lehman & Tomlinson 2004). Dermochelyoidea has a low branch support (Bremer support = 2) and has four unambiguous synapomorphies (two cranial; two postcranial, one of which is unique (ch. 237.1; Table 3). Cranial synapomorphies of dermochelyoids are shown in Figure 9. However, the less inclusive crown‐group Chelonioidea (i.e. Dermochelyoidea + Cheloniidae) and total‐group Chelonioidea (i.e. Toxochelys + Chelonioidea) have a high branch support with Bremer values of 4 and 5, respectively. This indicates that there is overall strong support for the placement of protostegids within Chelonioidea. The total group of Chelonioidea shares 21 unambiguous synapomorphies (Table 3; 11 cranial; 10 postcranial, 7 of which are unique (chs 255.2, 291.1, 295.0, 333.1, 334.1, 338.1, 342.1)). Crown‐group chelonioids (i.e. excluding Toxochelys) are united by seven unambiguous synapomorphies (three cranial, one of which is unique (ch. 93.2); four postcranial, two of which are unique (chs 306.1, 344.1)).Figure 9 Open in figure viewerPowerPoint Cranial synapomorphies of Dermochelyoidea illustrated by renderings of 3D models generated using CT data. A, cranium of Dermochelys coriacea (UMZC R3031) in ventral view, showing absence of medial process of jugal (ch. 27.0). B, cranium of Rhinochelys pulchriceps (CAMSM B55783) in ventral view, showing the same features as in A. C, cranium of Dermochelys coriacea (UMZC R3031) in dorsal view with the left postorbital removed, showing the opisthotic contribution to the foramen stepedio‐temporale (ch. 161.1). D, cranium of Bouliachelys suteri (QMF 31669) in dorsal view, showing the same features as in C. Abbreviations: fst, foramen stepedio‐temporale; j, jugal; op, opisthotic; pal, palatine. Scale bars represent: 20 mm (A, C, D); 1 mm (B). Colour online.
Protostegidae, including Archelon ischyros, Bouliachelys suteri, Desmatochelys lowii, Desmatochelys padillai, Notochelone, Ocepechelon bouyai, Protostega gigas, Santanachelys gaffneyi and Rhinochelys pulchriceps, is relatively well supported with a Bremer support of 3. Protostegids share eight unambiguous synapomorphies (Table 3; three cranial (Fig. 10); five postcranial, four of which are unique (chs 291.0, 328.1, 329.1, 335.1)). The in‐group relationships of Protostegidae differ in our analysis to those of most previous analysis. Commonly, Early Cretaceous protostegids such as Santanachelys, Bouliachelys, Notochelone and Rhinochelys are found as a paraphyletic grade leading to a clade of Late Cretaceous taxa, which includes Desmatochelys lowii, Archelon, and Protostega (e.g. Hirayama 1998; Kear & Lee 2006; Bardet et al. 2013). Bardet et al. (2013) found Ocepechelon in a polytomy with Bouliachelys, Santanachelys, other protostegids and dermochelyids. In our analysis, the gigantic Archelon and Protostega form a well‐supported clade (Bremer support = 7) that is sister group to all other protostegids. Within those, the Early Cretaceous taxa Santanachelys, Bouliachelys, Notochelone, Desmatochelys padillai and Rhinochelys, and the Late Cretaceous Desmatochely lowii form a well‐supported clade (Bremer support = 3) to the exclusion of the Late Cretaceous Ocepechelon. The clade including Ocepechelon has relatively strong support with a Bremer value of 3. Desmatochelys lowii and Desmatochelys padillai are sister taxa, as also found by Cadena & Parham (2015). The remaining protostegids from the Early Cretaceous (Bouliachelys, Rhinochelys, Notochelone, Santanachelys) are united in a clade that is well nested within the Protostegidae, despite their early branching positions in most other studies.Figure 10 Open in figure viewerPowerPoint Cranial synapomorphies of Protostegidae illustrated by renderings of 3D models generated using CT data. A, cranium of Rhinochelys pulchriceps (CAMSM B55783) in ventral view, showing the interpalatine contact (ch. 62.1). B, cranium of Rhinochelys pulchriceps (CAMSM B55783) in anterodorsal view, showing the lack of a medial contact between the prefrontals (ch. 4.0). C, posterior part of cranium of Rhinochelys pulchriceps (CAMSM B55783) in ventral view, showing the contact of the pterygoid with the mandibular articular surface of the quadrate (ch. 103.1). Abbreviations: pal, palatine; prf, prefrontal; pt, pterygoid; q, quadrate. Scale bars represent 1 mm. Colour online.
Various Asian and North American Mesozoic turtles that have classically been recovered on the stem of Cryptodira (Zhou & Rabi 2015) have been classified as sinemydids, macrobaenids or xinjiangchelyids (Brinkman & Wu 1999; Sukhanov 2000; Brinkman 2001; Parham & Hutchison 2003; Danilov et al. 2006; Rabi et al. 2010, 2014). These groups have been formalized by Rabi et al. (2014), who established phylogenetic definitions for the groups. One challenge to the application of these definitions is that they technically cannot be applied, if the ‘essential’ taxon of such a definition (i.e. the taxon used to define the clade) is not included in an analysis. In fact, the taxon used to define Macrobaenidae (Macrobaena mongolica) has, to our knowledge, never been included in a phylogenetic analysis, so that the taxonomic content of Macrobaenidae is entirely unclear.
We find taxa that have classically been assigned to the three groups defined by Rabi et al. (2014) in two monophyletic groups among the stem‐group of turtles as successive sister‐groups to Angolachelonia + crown‐group turtles. The group placed more crownward is comprised largely of Cretaceous species, and includes Sinemys lens (Late Jurassic; all other species in this list are Cretaceous), Sinemys gamera, Dracochelys biscuspis, Ordosemys sp., Judithemys sukhanovi, Kirgizemys dmitrievi and Kirgizemys hoburensis. Applying the phylogenetic definitions of Rabi et al. (2014), this entire group could be referred to as Sinemydidae. However, within our ‘Sinemydidae’, Sinemys lens and Sinemys gamera form a clade that is found in a polytomy with Dracochelys, Ordosemys, and a clade that includes Kirgizemys spp. and Judithemys, that is, species that are commonly referred to as macrobaenids (e.g. Gaffney & Ye 1992; Parham & Hutchison 2003). Depending on the (unresolved) phylogenetic position of Macrobaena mongolica, it is likely that our ‘Sinemydidae’ in fact comprises both sinemydids and macrobaenids. Therefore, we refer to the clade including Sinemys and Judithemys as Sinemydidae/Macrobaenidae throughout this work. Our Sinemydidae/Macrobaenidae is moderately supported by a Bremer support of 2, and the placement of sinemydids as the sister to Angolachelonia + crown‐group turtles also has a Bremer support of 2. Sinemydids/macrobaenids share two cranial and two postcranial synapomorphies, none of which are unique (Table 3).
The more stemwardly positioned group is comprised of Jurassic Asian turtles, and includes species of Xinjiangchelys and Annemys. Technically, the phylogenetic definition of Xinjiangchelyidae of Rabi et al. (2014) cannot be applied to this group, as we did not include the species of Xinjiangchelys used to define the group. However, for ease of communication, we refer to the group as Xinjiangchelyidae within this paper. Xinjiangchelyidae is moderately supported with a Bremer support of 2, although the in‐group relationships remain unclear in our analysis. Xinjiangchelyids share six unambiguous synapomorphies (three cranial; three postcranial, one of which is unique (ch. 257.1); Table 3). The node support for xinjiangchelyids plus all more crownwardly positioned turtles is high (Bremer support = 4).
Ordering characters resulted in 116 MPTs initially, and 195 MPTs 1566 steps long after additional TBR branch swapping. The results from the ordered analysis resulted in a large polytomy including all extant clades of turtles, xinjiangchelyids, angolachelonians, and the individual species of sinemydids/macrobaenids (Fig. 4B). This is caused by unstable positions of Angolachelonia, ‘macrobaenids’ (Judithemys + the species of Kirgizemys), and Ordosemys sp. and Dracochelys biscuspis. By inspecting the Adams consensus tree, we identified Ordosemys sp. as a ‘wildcard’ taxon that is alternatively found in clades with sinemydids/macrobaenids, only sinemydids or xinjiangchelyids. When Ordosemys is discarded from the set of MPTs, three main topologies are evident and are summarized in Figure 11. The MPT topologies include either: (1) Angolachelonians and ‘macrobaenids’ as successive sister groups to Toxochelys + chelonioids, making them stem‐group chelonioids; (2) only Angolachelonians as sister to Toxochelys + chelonioids, and sinemydids/macrobaenids forming a clade in the position in which they were also recovered in the unordered analysis; or (3) an identical topology to that of the unordered analysis. The topologies in which Angolachelonia is found on the stem‐group of chelonioids imply only one origin of marine lifestyles in non‐pleurodiran turtles besides Odontochelys. However, the ordered analysis agrees with the unordered one in always finding a monophyletic Angolachelonia, and always recovers protostegids as dermochelyoids.Figure 11 Open in figure viewerPowerPoint Competing MPT topologies of our ordered analysis resulting in a large polytomy. A, topology supported by a subset of MPTs that is identical with results from the unordered analysis. B, topology supported by a subset of MPTs in which angolachelonians and macrobaenids are stem‐group chelonioids. C, topology supported by a subset of MPTs in which angolachelonians, but not macrobaenids are stem‐group chelonioids. Note that Ordosemys has been pruned from the MPTs, and that protostegids are included in Chelonioidea.
Excluding ‘marine’ characters resulted in 86 MPTs 1480 steps long initially, and 104 MPTs were recovered in total after a second round of TBR branch swapping. This analysis resulted in a large polytomy that included pleurodires, trionychians, testudinoids, chelydroids, thalassochelydians, sandownids, Toxochelys and chelonioids (Evers & Benson 2018b, appendix S3, fig. S3.1). This polytomy resulted from the variable position of sandownids, which in some MPTs were found with thalassochelydians on the stem‐group of turtles, and in some MPTs forming a clade with Toxochelys on the stem‐group of chelonioids. In‐group relationships of Chelonioidea were poorly resolved, resulting a polytomy of protostegids, crown‐group cheloniids, dermochelyids, Eochelone, Allopleuron, Argillochelys and Puppigerus. However, protostegids were found to be chelonioids in all MPTs.
The ‘least specialized taxa analysis 1’ (only using Santanachelys) resulted initially in 91 MPTs 1443 steps long, and 120 MPTs were recovered after a second round of TBR branch swapping. The ‘least specialized taxa analysis 2’ (Santanachelys and Rhinochelys included) resulted in 39 MPTs 1453 steps long, and an additional 3 MPTs recovered during a second round of TBR branch swapping. The ‘least specialized taxon analysis 3’ (only Archelon and Protostega excluded) resulted in 12 MPTs 1510 steps long, and a second round of TBR branch swapping did not recover any further MPTs. In the first analysis, Eochelone was found in a polytomy with dermochelyids and cheloniids, and Toxochelys and Santanachelys were found in a polytomy with crown‐group chelonioids (Evers & Benson 2018b, appendix S3, fig. S3.2). In the second analysis, Sanatanchelys and Rhinochelys formed a monophyletic Protostegidae as the earliest branching stem‐group chelonioids (Evers & Benson 2018b, appendix S3, fig. S3.3). Toxochelys was also recovered as a stem‐group chelonioid, and as the immediate sister‐taxon to crown‐group Chelonioidea. Eochelone was found as the earliest branching stem‐group cheloniid. When only Archelon and Protostega were excluded, the relationships of all taxa were as in our unordered analysis with the complete taxon sampling, that is, protostegids were found as dermochelyoids (Evers & Benson 2018b, appendix S3, fig. S3.4).
Of the alternative hypotheses of turtle interrelationships (see Table 4) that we tested, only one could be rejected based on significant or near‐significant p‐values: the hypothesis that protostegids fall outside Chelonioidea (discussed below). Alternative hypotheses for xinjiangchelyids, sinemydids and angolachelonians could not be rejected. A possible reason for this is illustrated in our similarity results, which show that these groups have relatively high similarity to various cryptodiran groups. Although these similarities in character scores are optimized to be homoplastic in our analysis, alternative interpretations require only few more steps (see Table 4 for differences in step‐length) in parsimony analysis and are thus not significantly different to our preferred tree topology.Table 4. Constraints and hypotheses for Templeton's test and test results Constraint Hypothesis Symmetric Distance Length Test statistic N p All fossil unconstrained Topology as in Fig. 4A – 1532 – – – Plesiochelys etalloni as a stem‐group cryptodire (Constraint 1) Plesiochelyids are stem‐group cryptodires Maximum 1536 −452.5 44 0.2918 Minimum −3.5 6 0.0513c c Low p‐value due to small N. Jurassichelon oleronensis as a stem‐group chelonioid (Constraint 2) Plesiochelyids are stem‐group chelonioids Maximum 1536 −829.0 59 0.3196 Minimum −103.5 22 0.1969 Jurassichelon oleronensis as a stem‐group cryptodire (Constraint 3) Plesiochelyids are stem‐group cryptodires Maximum 1536 −473.5 45 0.2928 Minimum −3.5 6 0.0513c c Low p‐value due to small N. Solnhofia parsoni as a stem‐group cryptodire (Constraint 4) Thalassochelydia are stem‐group cryptodires Maximum 1536 −452.5 44 0.2018 Minimum −3.5 6 0.0513c c Low p‐value due to small N. Solnhofia parsoni as a stem‐group chelonioid (Constraint 5) Thalassochelydia are stem‐group chelonioids Maximum 1536 −829.0 59 0.3196 Minimum −103.5 22 0.1969 Sandownia parsoni as a stem‐group cryptodire (Constraint 6) Sandownids are stem‐group cryptodires Maximum 1536 −351.0 39 0.2686 Minimum −3.5 6 0.05125c c Low p‐value due to small N. Sandownia harrisi as a stem‐group chelonioid (Constraint 7) Sandownids are stem‐group chelonioids Maximum 1534 −565.0 48 0.3952 Minimum −162.0 26 0.3475 Rhinochelys pulchriceps as a stem‐group cryptodire (Constraint 8) Protostegids are stem‐group cryptodires Maximum 1548 −1538.5 86 0.0536d d Low p‐values that we refer to as near‐significant in the main text. Minimum −966.5 70 0.0334b b Significant at p < 0.01. Rhinochelys pulchriceps as a stem‐group turtle (Constraint 9) Protostegids are stem‐group turtles Maximum 1548 −1684.0 89 0.0727d d Low p‐values that we refer to as near‐significant in the main text. Minimum −598.5 57 0.0195b b Significant at p < 0.01. Xinjiangchelys wusu as a stem‐group cryptodire (Constraint 10) Xinjiangchelyids are stem‐group cryptodires Maximum 1538 −1088.5 68 0.2857 Minimum −646.0 53 0.2535 Sinemys lens as a stem‐group cryptodire (Constraint 11) Sinemydids are stem‐group cryptodires Maximum 1536 −829.0 59 0.3196 Minimum −247.5 33 0.2525 Judithemys sukhanovi as a stem‐group cryptodire (Constraint 12) Macrobaenids are stem‐group cryptodires Maximum 1536 −829.0 59 0.3196 Minimum −247.5 33 0.2525 Protostega gigas as a stem‐group cryptodire (Constraint 13) Protostegids are stem‐group cryptodires Maximum 1553 −1252.5 81 0.0153b b Significant at p < 0.01. Minimum −375.0 50 0.00195b b Significant at p < 0.01. Protostega gigas as a stem‐group turtle (Constraint 14) Protostegids are stem‐group turtles Maximum 1553 −1873.5 96 0.0315b b Significant at p < 0.01. Minimum −580.5 59 0.0047b b Significant at p < 0.01. Xinjiangchelys wusu as a stem‐group chelonioid (Constraint 15) Xinjiangchelyids are stem‐group chelonioids Maximum 1542 −855.0 63 0.1192 Minimum −638.0 55 0.1074 Sinemys lens as a stem‐group Chelonioid (Constraint 16) Sinemydids are stem‐group chelonioids Maximum 1537 −870.0 61 0.2695 Minimum −304.0 37 0.2056 Judithemys sukhanovi as a stem‐group chelonioid (Constraint 17) Macrobaenids are stem‐group chelonioids Maximum 1537 −870.0 61 0.2695 Minimum −304.0 37 0.2056 Santanachelys gaffneyi as a stem‐group cryptodire (Constraint 18) Protostegids are stem‐group cryptodires Maximum 1548 −1495.0 85 0.0495b b Significant at p < 0.01. Minimum −966.5 70 0.0334b b Significant at p < 0.01. Santanachelys gaffneyi as a stem‐group turtle (Constraint 19) Protostegids are stem‐group turtles Maximum 1547 −594.0 56 0.0309b b Significant at p < 0.01. Minimum −128.0 31 0.0036b b Significant at p < 0.01. Santanachelys gaffneyi as a stem‐group chelonioid (Constraint 20) Protostegids are stem‐group chelonioids Maximum 1534 −770.0 56 0.3981 Minimum −115.0 22 0.3349
Our procedure of using only one OTU to set up the constraints allowed us to additionally explore the topological effects of these hypotheses. In many cases, alternative placements of individual OTUs resulted in strong topological deviations from our original analysis and affected positions of taxa not relevant to the constraint. Some groups recovered in our analysis are also relatively unstable; for instance, our monophyletic Sinemydidae/Macrobaenidae is broken into paraphyletic or even polyphyletic assemblages in many of the constrained analyses. On the other hand, some groups, such as Angolachelonia or Xinjiangchelyidae, are relatively robustly recovered as monophyletic groups among the constrained analyses, even if their position within the tree structure varied. Consensus trees and MPTs for all constraint analyses in Newick tree format are provided in Evers & Benson (2018b); consensus trees are figured in Evers & Benson (2018b, appendix 3, figs S3.5–24).
Angolachelonia was recovered as a monophyletic group regardless of constraints on the positions of individual thalassochelydians (Plesiochelys, Jurassichelon or Solnhofia; Evers & Benson 2018b, appendix S3, figs S3.5–9), and when Sandownia is constrained to be a stem‐group cryptodire (Evers & Benson 2018b, appendix S3, fig. S3.10). In other words, specifying an alternative position for one of its members generally resulted in all members of Angolachelonia being found in that position. The one exception to this occurs when Sandownia was constrained to be a stem‐group chelonioid, in which case only sandownids followed Sandownia into this position, and Thalassochelyida was recovered on the stem‐group of turtles (Evers & Benson 2018b, appendix S3, fig. S3.11). None of the constrained analyses in which any member of Angolachelonia was included could be rejected (p > 0.05; constraint analyses required between two and four additional steps; see Table 4).
We could not reject the hypothesis that xinjiangchelyids (i.e. Xinjianchelys wusu) or sinemydids/macrobaenids (Sinemys lens or Judithemys sukhanovi) are stem‐group cryptodires (p > 0.05; four or six additional steps required; see Table 4). Constraining xinjiangchelyids to be stem‐group cryptodires resulted in a large polytomy that includes a clade comprising pleurodires and paracryptodires, a monophyletic Xinjiangchelyidae, sinemydids/macrobaenids (not forming a single clade), all cryptodiran clades recovered in our original analysis, and a monophyletic Angolachelonia (Evers & Benson 2018b, appendix S3, fig. S3.14). Constraining any member of our Sinemydidae/Macrobaenidae to be stem‐group cryptodires did not change the position of xinjiangchelyids as stem‐group turtles but resulted in the recovery of Angolachelonia as part of the total‐group of Chelonioidea, and the recovery of sinemydids/macrobaenids as a clade of stem‐group cryptodires (Evers & Benson 2018b, appendix S3, fig. S3.15–17).
Alternative hypotheses in which xinjiangchelyids or sinemydids/macrobaenids were stem‐chelonioids could not be rejected (sinemydids/macrobaenids: p > 0.05; five additional steps required; see Table 4), although p‐values for the constraint including Xinjiangchelys wusu were relatively low and tree length was relatively high (tree length = 1542 steps, i.e. 10 additional steps; maximum distance tree: p = 0.12; minimum distance tree: p = 0.11). When xinjiangchelydis were constrained to be stem‐group chelonioids, xinjiangchelyids and sinemydids formed a monophyletic group, and Angolachelonia was found on the stem‐group of turtles (Evers & Benson 2018b, appendix S3, fig. S3.19). When sinemydids were constrained to be stem‐group chelonioids, Angolachelonia was recovered the immediate sister to Chelonioidea and Toxochelys, and therefore more crownward on the cheloinioid stem than the sinemydids, which formed a clade (Evers & Benson 2018b, appendix S3, fig. S3.20–21). In these analyses, xinjiangchelyids were found to be stem‐group turtles.
We conducted an analysis in which Santanachelys gaffneyi was constrained to be a stem‐group chelonioid. This was done because this topology was found in our ‘least specialized taxa analysis 1’. This phylogenetic hypothesis could not be rejected statistically (tree length = 1534, i.e. two additional steps; maximum and minimum distance trees p > 0.5). This constraint resulted in a large polytomy among chelonioids (Evers & Benson 2018b, appendix S3, fig. S3.24). We additionally explored the Adams consensus tree, in which all fossil cheloniids were found to be members of the chelonioid stem‐group: Dermochelyidae (including Eosphagis) was sister to a clade comprising extant cheloniids, and taxa recovered as stem‐cheloniids in our original analysis formed a paraphyletic grade leading to crown‐group chelonioids. A monophyletic Protostegidae formed the next successive sister taxon, and Toxochelys was found as the earliest branching stem‐group chelonioid. Angolachelonia, Sinemydidae/Macrobaenidae and Xinjiangchelyidae were recovered in positions identical to those in the original analysis.
Constraining protostegids into alternative positions in the stem‐group of either cryptodires or turtles resulted in statistically significant or near significant p‐values, suggesting that alternative hypotheses are unlikely, although not always decisively rejected (see Table 4). The topological effects of these constraints resulted in major differences to our trees. When Rhinochelys or Santanachelys were constrained to be stem‐group cryptodires (tree length = 1548, i.e. 16 additional steps for either constraint; Rhinochelys: maximum distance tree p = 0.054; minimum distance tree p = 0.033; Santanachelys: maximum distance tree p = 0.0495; minimum distance tree p = 0.033) or stem‐group turtles, protostegids were found to be polyphyletic. The topological effects of these constraints were identical when Rhinochelys or Santanachelys were constrained to be stem‐group cryptodires (Evers & Benson 2018b, appendix S3, fig. S3.12, 22): Archelon and Protostega formed a clade on the stem of Dermochelys as crown‐group chelonioids, and the remaining protostegids were found as a monophyletic group that was sister to Thalassochelydia. Sandownids formed a clade one node more stemwardly positioned than the clade that includes Santanachelys or Rhinochelys and thalassochelydians. When Santanachelys was constrained to be a stem‐group turtle (tree length = 1547, i.e. 15 additional steps; maximum distance tree p = 0.031; minimum distance tree = 0.004) it was recovered as a plesiochelyid but all remaining protostegids were found to be dermochelyoids (Evers & Benson 2018b, appendix S3, fig. S3.23). Constraining Rhinochelys to be a stem‐group turtle (tree length = 1548, i.e. 16 additional steps; maximum distance tree p = 0.07; minimum distance tree = 0.02) resulted in the formation of a clade that included all protostegids except Archelon and Protostega (which remained dermochelyoids), plesiochelyids, and a clade including Solnhofia and sandownids (to which the phylogenetic definition of Angolachelonia sensu Mateus et al. (2009) can be applied, but which differs in taxonomic content of the Angolachelonia in our original analysis) (Evers & Benson 2018b, appendix S3, fig. S3.13).
When Protostega was constrained to be a stem‐group cryptodire (tree length = 1553, i.e. 21 additional steps; maximum distance tree p = 0.015; minimum distance tree p = 0.002), a monophyletic Protostegidae was recovered as the sister group to Angolachelonia (Evers & Benson 2018b, appendix S3, fig. S3.17). This clade was the immediate sister group to cryptodires. Sinemydids/Macrobaenids were found to be paraphyletic, and with the stem‐group turtles. Xinjiangchelyids were also found to be stem‐group turtles. When Protostega was constrained to be a stem‐group turtle (tree length = 1553, i.e. 21 additional steps; maximum distance tree p = 0.032; minimum distance tree p = 0.005) a monophyletic Protostegidae was recovered as the sister‐taxon of plesiochelyids. This clade was the sister clade to sandownids and Solnhofia, which formed a monphyletic group (Evers & Benson 2018b, appendix S3, fig. S3.18). Sinemydids/macrobaenids and xinjiangchelyids were again recovered as clades within the stem‐group turtles. In all constraints including protostegids, sinemydids/macrobaenids and xinjiangchelyids were always found to be stem‐group turtles.
BP, Bernhard Price Institute, Johannesburg, South Africa; BSPG, Bayerische Staatsammlung für Paläontologies und Geologie, Munich, Germany; CAMSM, Sedgwick Museum of Earth Sciences, Cambridge, UK; CMNH, Cleveland Museum of Natural History, Cleveland, OH, USA; DMNH, Denver Museum of Nature and Science, Denver, CO, USA; FCG‐CBP, Fundación Colombiana de Geobiología, Dentro de Investigaciones Paleontológicas, Villa de Leyva, Colombia; FMNH, Field Museum of Natural History, Chicago, IL, USA; FUM, Fur Museum (Museum Salling), Fur, Denmark; FWMSH, Fort Worth Museum of Science and History, Forth Worth, TX, USA; IVPP, Institute of Vertebrate Paleontology and Paleoanthropology, Beijing, China; IW, Ingmar Werneburg private collection; KUVP, University of Kansas, Lawrence, KS, USA; MCZ, Museum of Comparative Zoology, Harvard University, Cambridge, MA, USA; MIWG, Museum of Isle of Wight Geology, Sandown, Isle of Wight; MNA, Museum of Northern Arizona, Flagstaff, AZ, USA; MNB, Naturhistorisches Museum Basel, Basel, Switzerland; MPEF, Museo Paleontológico Egidio Feruglio, Trelew, Argentina; NHMM, Natuurhistorisch Museum Maastricht, Maastricht, Netherlands; NHMUK, Natural History Museum, London, UK; NMS, National Museum of Scotland, Edinburgh, UK; OCPDEK, Office Chérifien des Phosphates, Khouribga, Morocco; OUMNH, Oxford University Museum of Natural History, Oxford, UK; PIMUZ, Paläontologisches Institut und Museum der Universität Zürich, Zurich, Switzerland; PIN, Paleontological Institute, Russian Academy of Sciences, Moscow, Russia; PMOL, Paleontological Museum of Liaoning, Shenyang Normal University, China; QM, Queensland Museum, Brisbane, Australia; SMF, Senckenberg Museum Frankfurt, Frankfurt, Germany; SMNS, Staatliches Museum für Naturkunde, Stuttgart, Germany; SMU, Shuler Museum of Paleontology, Southern Methodist University, Dallas, TX, USA; TM, Teylers Museum, Haarlem, Netherlands; TMM, Texas Memorial Museum, Austin, TX, USA; TMP, Royal Tyrell Museum, Drumheller, Alberta, Canada; UCMP, University of California Museum of Paleontology, Berkeley, CA, USA; UMZC, University Museum of Zoology, Cambridge, UK; USNM, United States National Museum, Washington, DC, USA; WGJ, Waler Joyce private collection; YPM, Yale Peabody Museum, New Haven, CT, USA; ZIN PH, Zoological Institute of Russian Academy of Sciences, Palaeoherpotological Collection, St Petersburg, Russia.Systematic palaeontology
The clade that includes all turtles more closely related to Eurysternum wagleri Meyer, 1839, Plesiochelys etalloni (Pictet & Humbert, 1857) and Thalassemys hugii Rütimeyer, 1873, than to Pelomedusa subrufa (Bonnaterre, 1789), Testudo graeca Linnaeus, 1758, Protostega gigas (Cope, 1871b), or Sandownia harrisi Meylan et al., 2000.
Thalassochelydia can be diagnosed on the basis of the following unambiguous synapomorphies: processus trochlearis oticum is limited to the medial part of the otic chamber, and a deep recess is present on the anterior surface of the quadrate medially to the processus trochlearis oticum (ch. 81.1); presence of a fossa on the posterodorsal surface of the floor or the supratemporal fossa (ch. 113.1); splenial present (ch. 185.0); costals lack lateral ossification, allowing the dorsal exposure of the distal end of ribs and the development of fontanelles only at the most anterior and posterior costals (ch. 210.2); rib free peripherals are present (ch. 211.1); vertebrals 2 to 4 are significantly broader than pleurals (ch. 224.0); central articulations of cervical vertebrae are not formed, cervical vertebrae are amphicoelous or platycoelous (ch. 278.0).
Thalassochelydia was defined by Anquetin et al. (2017) to provide a name for the group that includes Eurysternidae, Plesiochelyidae and Thalassemydidae. To retain the association of the clade name with this taxonomic content, we chose to modify the original definition of Thalassochelydia to exclude Sandownia harrisi (the type species of Sandowniidae).
Phylogenetic definitions have been recently proposed for several commonly recovered clades of Mesozoic turtles (Joyce et al. 2004; Mateus et al. 2009; Rabi et al. 2014; Cadena & Parham 2015; Anquetin et al. 2017). These definitions usually include one or several statements of taxa excluded from the definition, and therefore associate a name very specifically to a set of fossil species or higher taxa to the exclusion of others. For example, Anquetin et al. (2017, p. 329) provided a phylogenetic definition for their newly coined clade Thalassochelydia, which includes ‘all turtles more closely related to Eurysternon wagleri Meyer, 1839, Plesiochelys etalloni (Pictet & Humbert, 1857), and Thalassemys hugii Rütimeyer, 1873, than to Pelomedusa subrufa (Bonnaterre, 1789), Testudo graeca Linnaeus, 1758, or Protostega gigas (Cope, 1871b)’. Implicit in the definition of Thalassochelydia is that Anquetin et al. (2017) had a specific idea about the content of Thalassochelydia, i.e. the group that only includes plesiochelyids, eurysternids and thalassemydids.
However, there are difficulties with applying definitions like the one above, because some of the specifiers have not been included in any phylogenetic analysis (see also definitions of Rabi et al. 2014). For example, no probable thalassemydid has ever been included in a phylogenetic analysis, and the species suitable to define Eurysternidae (i.e. Eurysternon wagleri) has also not been included in comprehensive analyses (Anquetin et al. 2017). Therefore, the application of the name rests on various untested assumptions (such as that Thalassemys hugii is more closely related to Plesiochelys etalloni than to Protostega gigas).
Despite the lack of evidence of the phylogenetic positions of the exact taxa included in the phylogenetic definition of Thalassochelyida as proposed by Anquetin et al. (2017), the definition of this taxon seems justifiable on the basis of: (1) cladistic evidence that species within the hypodigm of the three traditional families have recently been found to form a clade (plesiochelyids and the putative eurysternid Solnhofia; Anquetin et al. 2015); and (2) informal comparative anatomical evidence suggesting the existence of the group (Anquetin et al. 2017).
If the definition for Thalassochelyida is applied to our phylogenetic results, in which we find a clade comprised of Solnhofia parsoni (a putative eurysternid), Plesiochelys etalloni (a plesiochelyid) and Sandownia harrisi (a sandownid) to the exclusion of protostegids, pleurodires and cryptodires, then sandownids are also included in Thalassochelydia. However, this extended Thalassochelydia would then become an objective junior synonym of Angolachelonia, which is a clade named by Mateus et al. (2009) that is phylogenetically defined as the clade containing Solnhofia and sandownids. ‘Thalassochelydia’ as intended by Anquetin et al. (2017) (i.e. not including sandownids) still exists in our topology, but as a less inclusive clade within the extended Thalassochelydia. We consider it useful to have clade names available for sandownids, thalassochelydians (sensu Anquetin et al. 2017) and the clade that includes both of the former. Therefore, it is either necessary to accept the synonymy of Thalassochelydia with Angolachelonia and erect a new name for what Anquetin et al. (2017) intended to be Thalassochelydia, or to change the definition of either Angolachelonia or Thalassochelydia. Because Angolachelonia has priority over Thalassochelydia, we modify the definition of Thalassochelyida to specifically exclude sandownids.
Angolachelonia can be diagnosed on the basis of the following unambiguous synapomorphies: the foramen stapedio‐temporale is concealed in dorsal view by the temporal skull roof (ch. 18.0); the posterior surface of the quadrate bears an infolding ridge ventral to the incisura columella auris (ch. 83.1); the articular process of the cranium is strongly posteriorly directed (ch. 84.1); the pterygoids are in a very long medial contact with one another, longer than the basisphenoid total length in midline (ch. 94.0); the pterygoid contacts the medial edge of the mandibular condyle when is seem in ventral view (ch. 103.1); the posterior margin of the coronoid has a deep notch (ch. 181.1); the coronoid bears a foramen at the anterior end, which leads from the fossa meckelii into the space between the mandibular rami (ch. 182.1); the coronoid process is relatively high and dorsally or posterodorsally pointed (ch. 184.1).
Mateus et al. (2009) recovered sandownids as more closely related to crown‐group cryptodires than to plesiochelyids, and erected the clade Angolachelonia for a group uniting Solnhofia parsoni with Angolachelys mbaxi, a sandownid not included in our analysis. Angolachelys was not included in our analysis because limited anatomical information is available; new material is in preparation (Octavio Mateus pers. comm. to SWE in 2015). However, if Angolachelys is in fact a sandownid, as found by previous analyses (Mateus et al. 2009; Tong & Meylan 2013; Cadena 2015), then this name is applicable to the clade that includes thalassochelydians (which include Solnhofia) and sandownids (which include Angolachelys). Unlike in the analysis of Mateus et al. (2009), Angolachelonia includes plesiochelyids as well as Solnhofia and sandownids according to our results. Although we find Solnhofia as sister to plesiochelyids, branch support for this is only moderate (Bremer support = 2). If future analyses show that Solnhofia is indeed more closely related to sandownids than to plesiochelyids or other thalassemydids, Solnhofia would be removed from Thalassochelydia, and Angolachelonia would become applicable to the less inclusive clade of sandownids + Solnhofia.
The clade that includes Sandownia harrisi Meylan et al., 2000, but not Pelomedusa subrufa (Bonnaterre, 1789), Testudo graeca Linnaeus, 1758, Solnhofia parsoni Gaffney, 1975b, Eurysternum wagleri Meyer 1839, Plesiochelys etalloni (Pictet & Humbert, 1857), Thalassemys hugii Rütimeyer, 1873, or Protostega gigas (Cope, 1871b).
Sandownidae can be diagnosed on the basis of the following unambiguous synapomorphies: weak to no lower temporal emargination, the margin of the lower temporal emargination is formed by the quadratojugal or quadratojugal and jugal (ch. 34.0); a vomer–palatine contact anterior to the internal naris is present (ch. 57.1); the vomer contributes to the upper triturating surface (ch. 68.1); the pterygoid forms a posteromedial wing that partially or completely covers the parabasisphenoid, and sometimes the basioccipital in ventral view (ch. 108.1); the dorsum sellae is deep (i.e. the dorsal surface of parabasisphenoid between the clinoid processes is a transversely concave floor forming a trough between the posterior part of the dorsal surface of the parabasisphenoid, which is usually cup‐like, and the anterior portion of the parabasisphenoid forming the rostrum basisphenoidale and sella turcica) (ch. 139.0).
A monphyletic group including Sandownia harrisi, Brachyopsemys tingitana, Angolachelys mbaxi and Leyvachelys cipadi has been recognized in several studies (Mateus et al. 2009; Tong & Meylan 2013; Cadena 2015) and the group has been named as a family following a rank‐based definition by Tong & Meylan (2013). Here, we provide a phylogenetic definition of the group that is in accordance with the associated taxon‐content of the group implied by previous studies, and phrased coherently in comparison with other phylogenetic definitions for Mesozoic turtles.
Our phylogenetic results using unordered character states support the hypothesis of two independent origins of marine ecologies among non‐pleurodiran turtle from the Jurassic onwards: Angolachelonia (thalassochelydians + sandownids) and Chelonioidea (including protostegids). In addition to the Triassic stem‐group turtle Odontochelys, and 2–3 origins among pleurodires (depending on the phylogenetic relationships of Bothremydidae; Gaffney et al. 2006; Rabi et al. 2012), this demonstrates a total of 5–6 origins of marine habits through the evolutionary history of turtles. Our study represents the first analysis with a large sample of thalassochelydians and sandownids, in which these groups are found to form a clade. The only previous study with a similar sample size for these groups (Cadena 2015), recovered a polyphyletic Thalassochelydia (Plesiochelys was recovered as a stem‐group turtle, and Solnhofia and Jurassichelon were found to be stem‐group chelonioids) and sandownids as stem chelonioids. Compared to previous analyses, we included more observations regarding the cranial anatomy of turtle groups. This was possible thanks to 3D models derived from CT data for species of all major subgroups of turtles included in our taxon sampling, including several sandownids, thalassochelydians, protostegids and non‐protostegid chelonioids. However, alternative hypotheses in which angolachelonians are found to be stem‐group chelonioids cannot be rejected at present. Indeed, a parsimony analysis using ordered character states of our data supports this hypothesis in a subset of the resulting MPTs. If angolachelonians are indeed in the stem‐group of Chelonioidea, this would imply only a single origin of marine ecology outside pleurodires and Odontochelys. Angolachelonians are known from Jurassic, Cretaceous and Palaeogene deposits (e.g. Tong & Meylan 2013; Cadena 2015). Furthermore, marine bothremydids and chelonioids are also known both before and after the Cretaceous–Palaeogene boundary. Our results therefore indicate that all three major clades of Cretaceous marine turtles survived the K/Pg mass extinction. This contrasts with other marine reptiles, such as mosasaurs and plesiosaurs (Bardet 1994; Motani 2009; Benson 2013) and explanations of marine turtle survival warrant further investigation.
Differences in the nature of marine adaptation are evident among clades. Members of Angolachelonia are generally interpreted to live in shallow, nearshore marine habitats, because these turtles lack osteological evidence for a pelagic lifestyle, and are found in relatively nearshore deposits (Anquetin et al. 2017). Marine pleurodires such as bothremydids also lack evidence for a pelagic ecology, and are usually interpreted as having lived in near‐shore marine environments (e.g. Gaffney et al. 2006; Ferreira et al. 2018). Features interpreted to indicate a pelagic lifestyle, such as rigid inter‐phalangeal articulations in the manus, are only present in chelonioids, including protostegids. Because protostegids are found as chelonioids within our analysis, a pelagic lifestyle can be inferred to have evolved only once within turtles. Evolutionary refinement of key adaptations such as flippers cannot be resolved until a better understanding of the in‐group relationships of protostegids is obtained.
The Early Cretaceous protostegid Santanachelys gaffneyi has flippers in which some moveable articulations are still retained; a condition that is also present in Toxochelys (Hirayama 1998). This observation caused Hirayama (1994, 1998) to infer that derived flippers, with rigid manual articulations, evolved independently in dermochelyids, cheloniids and advanced protostegids. However, S. gaffneyi is nested deeply within Protostegidae in our analysis, and Toxochelys is found as a stem‐group chelonioid rather than a stem‐group cheloniid as in Hirayama (1998). Therefore, the presence of less specialized flippers in Santanachelys is optimized as a reversal, and the derived condition of flippers in which all manual articulations are rigid is optimized as a synapomorphy for crown‐group chelonioids (this was also implied by the matrix of Kear & Lee (2006), although not specifically stated). Unfortunately, the flipper morphology of most Early Cretaceous protostegids (e.g. Notochelone costata, Rhinochelys pulchriceps) is not known. However, Desmatochelys padillai from the Early Cretaceous of Colombia has been scored as having the advanced flipper condition (Cadena & Parham 2015), and Late Cretaceous protostegids also lack movable articulations (Hirayama 1994). In‐group relationships of Protostegidae require further investigation, because our phylogenetic results differ from those of previous analyses. If protostegids with derived flippers are found to be nested within protostegids showing the primitive condition (as in most previous studies), the flippers of protostegids and other chelonioids could have evolved convergently.
Protostegids have been hypothesized to be either: (1) on the stem‐group of the leatherback turtle Dermochelys coriacea within Chelonioidea (i.e. as dermocheyloids; Hirayama 1994, 1998; Brinkman et al. 2006; Kear & Lee 2006; Bardet et al. 2013; Cadena & Parham 2015; Cadena 2015); (2) an independent lineage of pelagic turtles on the stem‐group of cryptodires (Danilov & Parham 2006, 2008; Joyce 2007; Sterli & de la Fuente 2011, 2013; Anquetin 2012); or (3) on the turtle stem (Sterli 2010; Sterli & de la Fuente 2011). The finding of protostegids as stem‐group cryptodires, and therefore outside Chelonioidea by previous analyses, has always been based on the inclusion of the early protostegid Santanachelys as the sole representative of that group (Danilov & Parham 2006, 2008; Joyce 2007; Sterli & de la Fuente 2011, 2013; Anquetin 2012). Dermochelyoid affinities for protostegids are usually based on studies focused on the relationships of marine turtles (e.g. Hirayama 1994; Kear & Lee 2006; Bardet et al. 2013; Gentry et al. 2018), although some global studies have found protostegids in the same position (e.g. Cadena & Parham 2015; Cadena 2015).
Our matrix includes nine protostegids covering their temporal and geographical spread, body size range, and ecological adaptations. Skulls of three Early Cretaceous protostegids, Rhinochelys pulchriceps, Bouliachelys suteri and Notochelone costata, were CT‐scanned and complete skull models have been produced to facilitate character scoring. Our 3D models provide the most detailed account of the cranial osteology of protostegids. This allowed us to score numerous characters, which previously could not be scored, as well as formulate new characters, describing variation in the skull, and particularly the braincase. We find protostegids as dermochelyoids, and the total‐group and crown‐group of Chelonioidea, as well as Dermochelyoidea (i.e. Dermochelyidae + Protostegidae) are supported by a long list of unambiguous synapomorphies. Furthermore, Bremer support for these groups is robust (see Results, above).
It has been suggested that the finding of protostegids as chelonioids results from the convergent acquisition of a high number of phylogenetically‐misleading anatomical character states related to a pelagic lifestyle in both groups (Cadena & Parham 2015). To investigate this, we identified synapomorphies that support the chelonioid relationships of protostegids and could plausibly result from functional constraints on marine adaptation (Table 5). These include characters related to the reduction of shell ossification, the modification of limbs to flippers, formation of a secondary palate, and modifications of the triturating surface more generally that could be related to feeding. Several of these characters are also optimized as independently‐obtained synapomorphies of angolachelonians or angolachelonian subgroups (Table 5). Although we do not support the practice of deleting characters due to assumed ecological function, protostegids are still recovered as chelonioids by analysis excluding the characters listed in Table 5 (see Evers & Benson 2018b, appendix S3, fig. S3.1). This suggests that protostegids can be found as chelonioids independently of functionally convergent features related to marine or pelagic life. Our ‘least specialized taxa analyses’ provide further support for the hypothesis that protostegids are chelonioids, although they are found as stem‐group chelonioids rather than dermochelyoids when only the taxa from the Early Cretaceous (Santanachelys, Rhinochelys) are included. Nevertheless, our analysis is the first study in which protostegids are still allied with chelonioids when ‘advanced’ protostegids are excluded from the analysis.Table 5. ‘Marine’ synapomorphies Character state Description Synapomorphy Functional relevance 39.1 Lose squamosal–quadrate articulation Total‐group chelonioids; plesiochelyids ?Underwater hearing 58.1 Maxillary triturating surface with labial and lingual ridge Total‐group chelonioids; plesiochelyids Feeding 68.1 Vomer contributing to upper triturating surface Cheloniids; sandownids Secondary palate 210.2 Reduction of costal ossification Total‐group chelonioids; thalassochelydians Functional interpretation unclear 231.1 Presence of plastral fontanelle Total‐group chelonioids Functional interpretation unclear 333.1 Humerus longer than femur Total‐group chelonioids Swimming 337.1 Rigid articulations in first and second mandual digit Crown‐group chelonioids Swimming 338.1 Rigid articulations in third–fifth manual digits Total‐group chelonioids Swimming 342.1 Flattening of carpal and tarsal elements Total‐group chelonioids Swimming
Our heatmaps of similarity indicate that protostegids do show relatively high similarity with various non‐chelonioids among stem‐group turtles, particularly to sinemydids, xinjiangchelyids and angolachelonians. Similarities between protostegids and stem‐group turtles were also noted by Cadena & Parham (2015). While the high similarity of protostegids to sinemydids and xinjiangchelyids cannot be explained by ecological convergence, it is possible that at least some of the similarity between protostegids (and also chelonioids more generally) and angolachelonians can be explained by their marine lifestyle.
Our Templeton's tests provide explicit tests of hypotheses that protostegids are stem‐group turtles, or stem‐group cryptodires. These hypotheses, although not being strictly rejected in all cases (10 tests result in p < 0.05, and 2 tests result in 0.054 < p < 0.073; Table 4), have poor support despite the high amount of similarity of protostegid character scorings with those of the non‐chelonioid groups. Interestingly, when the Early Cretaceous protostegids Rhinochelys or Santanachelys are used to constrain protostegids into alternative positions, protostegids are found to be polyphyletic, with Late Cretaceous protostegids still being recovered as the sister to Dermochelyidae. In contrast, when Protostega was constrained to alternative positions, protostegids were found to be monophyletic. This provides an explanation for the frequent recovery of protostegids as non‐chelonioids, when the early protostegid Santanchelys was used as the only protostegid representative in phylogenetic analyses (Danilov & Parham 2006, 2008; Joyce 2007; Sterli & de la Fuente 2011, 2013; Anquetin 2012). Therefore, our matrix provides strong support for the position of protostegids within Chelonioidea. However, the hypothesis that protostegids are stem‐group chelonioids, rather than dermochelyoids, cannot be statistically rejected (p > 0.05; Table 4), and was also found in our ‘least specialized taxa analyses’ when only Early Cretaceous protostegids were included in the phylogenetic analysis.
Molecular phylogenies strongly support a sister‐group relationship between Chelydroidea (chelydrids + kinosternids) and Chelonioidea (e.g. Parham et al. 2006; Crawford et al. 2015; Pereira et al. 2017) as a clade called Americhelydia (Joyce et al. 2013). Estimates of divergence times place the chelonioid–chelydroid split in the late Early Cretaceous (113 Ma; Joyce et al. 2013) and the origin of crown‐group chelonioids in the latest Cretaceous (66 Ma; Joyce et al. 2013). The fossil calibrations used in these analyses represent the oldest specimens that can be assigned to the respective crown‐groups with high certainty (Joyce et al. 2013), and these specimens are generally younger than more ambiguous representatives such as protostegids. For example, protostegids, which are recovered confidently as crown‐group chelonioids in our analysis, are substantially older (Barremian–Aptian, 120 Ma) than the fossil calibration specimens used by Joyce et al. (2013) as the oldest crown‐group chelonioids (Eosphargis breineri from the Eocene, 55 Ma). Because the oldest protostegids are older than the molecular clock divergence time estimated for Americhelydia, our phylogenetic results have implications for the timings of deep divergences of the turtle crown‐group. Furthermore, the inclusion of protostegids within Chelonioidea has implications for the biogeographical evolution of Americhelydia.
The oldest unambiguous (although fragmentary) chelydrid and kinosternoid remains are from the Campanian of Mexico (Brinkman & Rodriguez de la Rosa 2006; Joyce et al. 2013; Joyce 2016; Joyce & Bourque 2016) and the USA (Lyson et al. 2017), and relatively complete specimens are known from the Maastrichtian of North America (Emarginachelys cretacea; Whetstone 1978; Hoplochelys clark; Knauss et al. 2011; Joyce & Bourque 2016). Furthermore, the oldest commonly accepted stem‐group chelonioid is Toxochelys from the upper Santonian or lower Campanian Niobrara Formation of North America (Nicholls 1988; Weems & Brown 2017; Gentry et al. 2018). Therefore, the earliest undisputed americhelydians suggest a North American origin of the clade (e.g. Crawford et al. 2015; Parham et al. 2014; Cadena & Parham 2015; Pereira et al. 2017) and their ages are consistent with molecular clock estimates dating the origin of Americhelydia into the late Early Cretaceous. A North American origin for Chelonioidea is also supported by a number of pre‐Maastrichtian fossils for which phylogenetic positions are currently uncertain, but which have been hypothesized to be either stem‐group chelonioids, stem‐group cheloniids or stem‐group dermochelyids, such as Ctenochelys (e.g. Matzke 2007; Gentry 2016) or Corsochelys (Zangerl 1960). Nevertheless, some poorly known fossils of Chelonioidea incertae sedis are also found in pre‐Maastrichtian deposits outside North America, such as the putative dermochelyid Mesodermochelys undulatus from the Santonian–Maastrichtian of Japan (Sato et al. 2012).
The oldest uncontentious crown‐group chelonioids are generally much younger than crown‐group chelydroid material and are not from North America. Although putative dermochelyid specimens are known from the Cretaceous, this mostly fragmentary material has not been included in a phylogenetic analysis (Joyce et al. 2013). Therefore, the oldest widely‐accepted dermochelyid is the Eocene Eosphargis breineri from Denmark (Wood et al. 1996; Joyce et al. 2013). Similarly, several Eocene taxa from Europe, including Argillochelys cuneiceps, Eochelone brabantica and Puppigerus camperi, have been consistently found as stem‐group cheloniids (e.g. Weems & Brown 2017) and this is supported by our analysis. Putative stem‐group cheloniids are also known from the Cretaceous (e.g. Brinkman et al. 2006, 2009; Parham et al. 2014; Gentry et al. 2018) but phylogenetic uncertainty surrounding these taxa has been used as an argument against their use as calibration points (Joyce et al. 2013). However, there is a growing body of evidence to suggest that some Cretaceous taxa which have been previously found in alternating phylogenetic positions (such as Ctenochelys from the Coniacian–Campanian of the USA, and Peritresius from the Campanian of the USA) can be firmly assigned to the stem‐group of cheloniids based on newly discovered or re‐analysed material (e.g. Gentry 2016; Gentry et al. 2018).
Minimum age constraints for fossil calibrations should be based on strong phylogenetic support indicating the taxon in question is actually a member of the crown‐group (Parham et al. 2012). Although we reject the possibility that protostegids fall outside the crown‐group of Cryptodira, we cannot reject the possibility that protostegids are stem‐group chelonioids. Therefore, protostegids might not be ideal candidates for constraining the crown‐group age of Chelonioidea, although they could be used as a calibration for the crown‐group of Americhelydia. Nevertheless, we find strong support for the presence of crown‐group members of Chelonioidea in the Cretaceous, even ignoring protostegids. For example, Allopleuron hofmanni from the Maastrichtian of central Europe is found as a stem‐group cheloniid. Irrespective of the affinities of protostegids (i.e. even if protostegids are not crown‐group chelonioids) the use of Allopleuron or even older taxa such as Ctenochelys or Peritresius (Gentry et al. 2018) as a calibration point for the crown‐group of Chelonioidea is likely to affect molecular clock estimates for the crown‐group age of chelonioids, and should be investigated. Although we do not provide a formal molecular clock analysis, we produced a time‐calibrated version of our tree using a posteriori calibration methods in R (see Material and Method, above), which illustrates the extensions of chelonioid ranges implied by our phylogenetic results (see Fig. 12).Figure 12 Open in figure viewerPowerPoint Simplified phylogenetic tree scaled to geologic time using range data for turtles.
The hypothesis of protostegids being crown‐group chelonioids complicates biogeographical scenarios for the evolution of Americhelydia (e.g. Joyce et al. 2013; Parham et al. 2014; Cadena & Parham 2015). This is because the cosmopolitan distribution of the earliest protostegids, lacking any records from the Early Cretaceous of North America, is hard to reconcile with the occurrence of earliest chelydroid and stem‐group chelonioid material exclusively in North America. Given the predominantly North American records of all of their close relatives, our phylogenetic results nevertheless imply a North American origin of protostegids, and therefore suggest an early, rapid, global dispersal for the group. The inferred marine ecology for all protostegids, including earliest members of the group (Cadena & Parham 2015), makes this hypothesis plausible. Furthermore, our hypothesized Late Cretaceous age for the chelonioid crown‐group also invokes rapid, early dispersal to explain the distribution of stem‐cheloniids in the Late Cretaceous; Maastrichtian, stem‐group cheloniids have a near‐global distribution, indicated by the presence of Allopleuron in Europe and the widespread distribution of Euclastes spp. (Parham et al. 2014). In the context of our phylogenetic hypothesis, it is also noteworthy that the ‘advanced’ protostegids Archelon and Protostega, which are known from the Santonian–Campanian of North America, are, contrary to earlier phylogenetic studies (e.g. Kear & Lee 2006), not deeply nested within the Protostegidae according to our analysis. This topology implies that the last common ancestor of protostegids originated in North America, but so far remains unsampled.
If protostegids are indeed crown‐group chelonioids, as proposed here, both chelydroids and cheloniids have relatively long ghost lineages of minimally 40 myr, ranging from the Campanian (the oldest occurrence of chelydroids) or the Maastrichtian (the oldest occurrence of cheloniids) back to the top of the Barremian (the oldest occurrence of protostegids; Cadena & Parham 2015). The cheloniid ghost lineage is significantly shortened, if Ctenochelys is accepted as a stem‐group cheloniid (Gentry 2016; Gentry et al. 2018). The alternative hypothesis, in which protostegids are not chelonioids (e.g. Joyce 2007; Danilov & Parham 2008; Sterli 2010; Anquetin 2012) reduces the ghost‐lineages for americhelydian crown‐groups, but in doing so implies a long ghost‐lineage for the americhelydian stem‐group that spans through the entire Early Cretaceous and into the early Late Cretaceous. Ghost‐lineages for various phylogenetic hypotheses are compared in Figure 13, and the biogeographical distributions of the earliest members of the different turtle clades considered in this study are indicated to compare biogeographical implications of these hypotheses. The (thus far unsampled) existence of Early Cretaceous americhelydians is not implausible because the sedimentary and fossil record of post‐Tithonian to pre‐Campanian tetrapods in North America is relatively poor, with only few tetrapod‐bearing formations known, and few turtle species of any groups (Ronov et al. 1980; Benson et al. 2013; Joyce et al. 2013; Nicholson et al. 2015). Therefore, the absence of chelydroid, non‐protostegid chelonioid, and protostegid fossils in the late Early and early Late Cretaceous of North America could be a taphonomic or discovery artefact.Figure 13 Open in figure viewerPowerPoint Implications of alternative positions of Protostegidae for americhelydian ghost‐lineages and biogeography illustrated by simplified calibrated trees. A, preferred hypothesis of this study, supported by unordered phylogenetic analysis. B, hypothesis placing Angolachelonia on the stem‐group of chelonioids, supported by a subset of MPTs in the ordered analysis. C, hypothesis of protostegids being stem‐group chelonioids, supported by a subset of our ‘least specialized taxa analyses’. D, hypothesis following Joyce (2007) and other authors in placing protostegids in close relation to thalassochelydians and sandownids, and having an extended cryptodiran stem‐lineage that further includes sinemydids/macrobaenids and xinjiangchelyids. Ghost lineages for americhelydian lineages are indicated by dashed arrows. Coloured squares indicate the distribution of earliest fossils according to continents.
Finally, an Early Cretaceous age for crown‐chelonioids, as implied by our phylogenetic hypothesis of protostegids, is not inconsistent with divergence time estimates for other groups of turtles, or with the oldest crown‐group turtle occurrences. The oldest unambiguous total‐group pleurodire is Caribemys oxfordiensis from the Oxfordian of Cuba (de la Fuente & Iturralde‐Vinent 2001; Joyce et al. 2013), and stem‐group pleurodires are also known from the Upper Jurassic of North America, South America and Europe (Platychelyidae; Lapparent de Broin et al. 2007; López‐Conde & Alvarado‐Ortega 2017; Sullivan & Joyce 2017), indicating that the cryptodire–pleurodire split occurred by the Late Jurassic. The origin of crown‐group Cryptodira has been dated by using representatives of the oldest documented cryptodiran clade, Trionychia (e.g. Joyce et al. 2013). The stem‐group trionychian Sinaspideretes wimani represents the oldest currently known material of Cryptodira, but the ambiguous locality information for specimens of this taxon make it difficult to use Sinaspideretes as a calibration point, as the possible age of the fossils range from the Middle Jurassic to the Early Cretaceous (Joyce et al. 2013; Tong et al. 2014). Therefore, Joyce et al. (2013) used stem‐trionychid remains from the Barremian (e.g. Hirayama et al. 2013; Joyce et al. 2013) as a minimum age constraint for Cryptodira, and dated the origin of Cryptodira to the Early Jurassic, a result that was partially driven by their soft maximum constraint at the base of the Jurassic. The oldest crown‐group trionychians are known from the Aptian and Albian (Tong et al. 2009; Joyce 2014; Li et al. 2015; Brinkman et al. 2017; Vitek et al. 2018) . Within Trionychia, trionychids have a well‐studied fossil record that indicates that the group was widely distributed and diverse in the Early Cretaceous (e.g. Hirayama et al. 2013; Danilov et al. 2014; Vitek & Joyce 2015; Joyce et al. 2016a, b; Georgalis & Joyce 2017). Similar patterns of diversification have been observed for Pleurodira: the oldest crown‐group pleurodire is Atolchelys lepida from the Barremian of Brazil (Romano et al. 2014). The pleurodire–cryptodire split and the origin of Trionychia represent early crown‐group turtle divergences. In contrast, chelonioids are deeply nested within Cryptodira. Therefore, although not inconsistent with the ages of major groups of crown‐group turtles in general, our results imply longer ghost lineages for at least some of the more deeply‐nested groups of Cryptodira than have previously been recognized.
The Early Cretaceous diversification of at least some higher clades of the turtle crown‐group (pleurodires, trionychids and chelonioids, as suggested here) is consistent with large increases in subsampled richness estimates for regional turtle assemblages during the Early Cretaceous (Nicholson et al. 2015). Our phylogenetic results suggest rapid diversification of crown‐groups of turtle subclades during this interval. This hypothesis will continue to be tested by new fossil discoveries, and re‐interpretation of existing specimens using methods like CT scanning.Conclusions
Our new phylogenetic matrix represents an effort to combine previously observed variation across non‐pleurodiran turtles with new observations informed by the study of high‐resolution CT scans. The character data has been vetted to directly reflect primary hypotheses of homology. The new phylogenetic hypothesis presented here supports two origins of marine ecology in non‐pleurodiran turtles outside Odontochelys. One of these is a newly recognized group, Angolachelonia, which includes thalassochelydians from the Late Jurassic, and sandownids from the Cretaceous and Palaeogene. Angolachelonians lack features indicative of a pelagic lifestyle, which are only present in chelonioids, supporting a single origin of pelagic ecology in turtles. Our results indicate extensive survivorship of marine turtles during the Cretaceous–Palaeogene mass extinction in comparison to other marine tetrapods, because members of all marine clades that were present at the end of the Cretaceous (i.e. bothremydid pleurodires, angolachelonians and chelonioids) survived into the Cenozoic. Furthermore, our analysis provides strong evidence for the position of protostegids within the crown‐group of chelonioids. Alternative positions for protostegids cannot be robustly statistically rejected in all cases, but these alternative hypotheses lack any substantial support from our data, and even the exclusion of ‘marine’ characters or a reduced taxon sampling only including early and less specialized taxa support our proposed relationships for protostegids. Previously proposed alternative positions for protostegids can be explained by high levels of similarity (i.e. homoplasy) to several turtle clades that are positioned more stemwardly and have been derived by using only a single early representative of the group, Santanachelys. The inclusion of protostegids, as well as some other taxa such as Allopleuron from the Maastrichtian, in the crown‐group of chelonioids implies an earlier diversification of the group than previously thought, and implies an Early Cretaceous age for the origin of the crown‐group of Chelonioidea. Although this needs further exploration, these findings are consistent with the hypothesis of rapid evolution and diversification of subclades of the turtle crown in the Early Cretaceous.Acknowledgements
This research was supported by a NERC studentship to SWE on the DTP Environmental Research (NE/L0021612/1) and further received support from the SYNTHESYS Project (http://www.synthesys.info/), which is financed by European Community Research Infrastructure Action under the FP7 ‘Capacities’ Program (grant awarded to SWE). We are thankful to all the curators who granted access to specimens under their care, namely: Carl Mehling and Mark Norell (AMNH); Oliver Rauhut (BSPG); Matt Riley (CAMSM); Jason Head (UMZC); William Simpson and Alan Resatar (FMNH); René Lyng Sylvestersen (FUR); Jérémy Anquetin (Jurassica); Alex Peaker (MIWG); Loïc Costeur (MNB); Sandra Chapman, Patrick Campbell and Paul Barrett (NHMUK); Hilary Ketchum (OUMNH); Alexander Kupfer and Rainer Schoch (SMNS); Jonah Choiniere and Bruce Rubridge (ESI at WITS), Anne Schulp (TM and Naturalis); Jessica Maisano, Matt Colbert and Chris Rowe (TMM). We further thank research and technical staff and PIs at the CT scanning facilities we used for this research, namely: Yi Hongyu (AMNH, IVPP); Tom Davies and Ben Moon (University of Bristol), Farah Ahmed (NHMUK), Zhe‐Xi Luo and April Isch Neander (University of Chicago). We thank Stephanie Wright for help with segmenting our specimen of Dermochelys. We are also grateful to colleagues who shared CT data and/or pictures of turtle material, specifically but in no particular order: Paul Barrett, Marc Jones, Don Brinkman, Thorsten Scheyer, Ingmar Werneburg, Walter Joyce, Gabriel Ferreira, Stephan Lautenschlager and Jérémy Anquetin. David Ford, Hermione Beckett, James Neenan, Erin Saupe, Gabriel Ferreira, Márton Rabi, James Parham, Donald Davesne and Gemma Benevento are thanked for discussions. We are thankful for the constructive and helpful reviews of Juliana Sterli and James Parham, which improved a previous version of this work. TNT is made freely available through the Willi Henning Society.