2.2.1. The skull

The skull is preserved in palatal view and the palate is rather badly crushed so that no sutures can reliably be distinguished. Nevertheless, certain details, particularly on the right side, can be determined. For example, the contact between the maxilla and palatine is quite well exposed but there is no evidence of a suborbital fenestra. More anteriorly there is a narrow opening in the palate that we interpret as the posterior end of the right internal naris. Also, on the right side, the transverse process of the pterygoid, which would have articulated with, and ventrally overlapped, the ectopterygoid, is visible. It is characterised by a well-defined ridge that curves anterolaterally from the margin of the interpterygoid vacuity, but there is clearly no development of any ventrally directed pterygoid-ectopterygoid flange. This is a feature that is preserved even more clearly in IVPP V17977 (see below). Rieppel et al. (Reference Rieppel, Li and Fraser2008) postulated that the pterygoids met posteriorly along the midline and possibly even covered the basicranium. However, with the discovery of IVPP V17977, we now know that this is an artifact of preservation, and that the basioccipital and parabasisphenoid must be displaced in this specimen. The posterior end of the right mandibular ramus is well preserved and, as noted previously (Rieppel et al. Reference Rieppel, Li and Fraser2008), supports earlier observations that the retroarticular process is considerably reduced in Dinocephalosaurus orientalis.

2.2.2. The cervical series

Behind the skull, the centrum of the atlas is preserved in direct articulation with the axis. As previously described (Rieppel et al. Reference Rieppel, Li and Fraser2008), an additional 16 cervical vertebrae are articulated as a series behind the axis (making a total of 18 cervical vertebrae) before there is a clean break in the column. Following this an additional series of seven articulated cervical vertebrae extends at a right angle to the proximal 18 cervical vertebrae and in close association with a tight bundle of cervical ribs. It is not clear whether there are any cervical vertebrae missing at this first break in the axial skeleton, although it seems unlikely as there are no isolated sections of rib that cannot be matched with either of the two articulated sections.

There then follows a second break in the cervical column corresponding to a point between cervical 25 and 26. Here it appears that cervical 26 and 27 have been displaced and ‘twisted’ out of alignment with the rest of the column (Fig. 2) and are slightly disarticulated. Rieppel et al. (Reference Rieppel, Li and Fraser2008) were unable to come to any definitive conclusion on the number of cervical vertebrae, but based on a discernible reduction in length of the centra considered it most likely that the next vertebra in the series represented the first dorsal, despite the fact that the pectoral girdle is situated more posteriorly. However, we now know that in some long-necked early archosauromorphs, for example Tanystropheus spp., there is a distinct shortening of the most posterior cervical vertebrae compared to the anterior and mid cervical vertebrae. In this case the vertebrae can still be distinguished as cervical vertebrae based on their association with characteristic plough-shaped ribs (Rieppel et al. Reference Rieppel, Jiang, Fraser, Hao, Motani, Sun and Sun2010), although those ribs are much shorter and more robust than the more anterior cervical ribs. Based on this knowledge it is now apparent that there are at least five additional vertebrae behind cervical 27 that are associated with shortened rather plough-shaped ribs with very robust heads. Thus, we consider this individual to show at least 32 cervical vertebrae. The ribs associated with vertebrae 28 and 29 have a clear anterior process, but this becomes less pronounced in the next three vertebrae. Nevertheless, they have greatly thickened heads that turn in sharply towards their articulations with the vertebrae. However, the exact distinction between the cervical and dorsal series remains somewhat equivocal as the region around the pectoral girdle is rather poorly preserved. Indeed, details of much of the trunk region, including the pectoral and pelvic girdles, are rather indistinct.

Rieppel et al. (Reference Rieppel, Li and Fraser2008) recorded the presence of the right ilium and pubis in fairly close association although not in complete articulation. The posterior edge of the pubis is relatively straight and lacks any posterior emargination. This is a condition that is confirmed by examination of ZMNH M8752 and IVPP V20295 (see below). Dinocephalosaurus orientalis therefore lacked a thyroid fenestra entirely. A thyroid fenestra is present in most tanystropheids, but it is absent in Tanytrachelos ahynis and Fuyuansaurus acutirostris, and in the probable non-tanystropheid archosauromorph Jesairosaurus lehmani (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). The ilium possesses a well-defined facet for the ischium set off from that for the pubis (Rieppel et al. Reference Rieppel, Li and Fraser2008), but the ischium appears to be missing completely and therefore did not form a fused pubo-ischiadic plate with the pubis, similar to other early archosauromorphs. There may even have been a slight separation of the ischium and pubis along their ventral symphysis.

2.3.1. The skull

The dermal palate is nearly closed in Dinocephalosaurus orientalis. Although beautifully exposed and lacking the level of crushing seen in IVPP V13898, it is still difficult to clarify details of the sutures, particularly between the palatines and the pterygoid. Some of the clearest are the interdigitating sutures separating the vomers from the pterygoids, and on the right side there appears to be a fairly well-defined suture between the palatine and vomer (Fig. 3b). Lateral to this suture, the posterior margin of the internal naris is clearly visible on the right side bounded by the palatine. A suborbital fenestra is absent, and the broad palatal rami of the pterygoids meet each other at the midline for most of their length. The contact between them is established shortly in front of the open palatobasal articulation. The palatal ramus of the pterygoid meets the ectopterygoid and palatine laterally and the broad vomer anteriorly, thus separating the paired palatines from each other along the midline. The very wide palatal ramus of the pterygoid resembles the condition seen in Tanystropheus hydroides (Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b) and contrasts with the much narrower pterygoid seen in other tanystropheids and early archosauromorphs (e.g., Macrocnemus spp., Miedema et al. Reference Miedema, Spiekman, Fernandez, Reumer and Scheyer2020; Scheyer et al. Reference Scheyer, Wang, Li, Miedema and Spiekman2020, and Azendohsaurus madagaskarensis, Flynn et al. Reference Flynn, Nesbitt, Michael Parrish, Ranivoharimanana and Wyss2010). The boundaries between the palatines and pterygoids are completely indistinct. On the left side of the palate there is a prominent ridge running anteroposteriorly for at least two-thirds of the length of the entire palate (Fig. 3b). While superficially this appears to be an articulation between the two elements, significantly it is not repeated on the right side and it is completely inconsistent with the configuration of the palatine and pterygoid in other diapsids. A long connection with the palatine along the lateral margin of the palatal ramus of the pterygoid can also be observed in dorsal view through the orbit in IVPP V20295 (see below). Therefore, the condition of the left side of the palate of IVPP V13898 is considered to be an artifact of preservation. Likewise, there is no obvious separation between the ectopterygoid and pterygoid. As noted above for IVPP V13898, there is a very clear ridge that essentially demarcates the anterior boundary of the pterygoid transverse process. This is preserved symmetrically on both sides but does not seem likely to represent the ectopterygoid-pterygoid boundary. Nor does it seem to represent an impression resulting from the extreme compression of the dorsal roof of the skull since its position is inconsistent with the position of either the orbital margins or the borders of the temporal fenestrae. We therefore regard this ridge as a characteristic feature of Dinocephalosaurus orientalis. The posterolateral corner of the transverse process of the pterygoid is curved posteriorly and hook-shaped in ventral view, which is a condition that is also found in Jesairosaurus lehmani, Tanstropheus spp., Amotosaurus rotfeldensis and certain allokotosaurs among early archosauromorphs (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). This posterior hook of the transverse flange of the pterygoid is absent in Macrocnemus spp. and Prolacerta broomi.

Although the palate would seem to be generally devoid of any dentition, there are the possible remnants of two small denticles preserved on what is taken to be the posterior edge of the right palatine just anterior to the transverse process of the pterygoid. Palatal dentition is present on the pterygoid, vomer and palatine in most non-archosauriform archosauromorphs in which these regions have been observed (Ezcurra Reference Ezcurra2016; Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). However, Tanystropheus hydroides also shows a distinct reduction in palatal dentition, since it only possesses a single row of well-developed teeth along the outer margin of the vomer (Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b).

The quadrate process of the pterygoid is broad and distinctly curved posterolaterally, its deeply concave lateral margin defining the medial contours of the relatively short subtemporal fenestra. The quadrate process of the pterygoid terminates in a blunt tip that contacts the medial aspect of the quadrate narrowly above its mandibular condyle.

Between the quadrate rami of the pterygoids the basicranium is exposed in ventral view. The ventral surface of the parabasisphenoid posterior to the palatobasal articulation is concave. Little morphological detail is discernible in the crushed bone that comprises the basioccipital, occipital condyle and the atlas centrum and neural arches. The first cervical ribs appear to have been articulating on the atlas. The right exoccipital and opisthotic are well preserved and exposed, however, indicating lack of fusion of these two elements. The exoccipital and opisthotic are generally not fused in mature specimens of non-archosauriform archosauromorphs, with the exception of Tanystropheus hydroides and certain allokotosaurs (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021).

2.3.2. The mandible

The articulated mandible is exposed in ventral view. On the left mandibular ramus, a faint suture may represent the boundary of the splenial, but its boundaries remain unclear. In the right mandibular ramus, below the mandibular joint, the angular is exposed as a distinct medial expansion. The retroarticular process projects only slightly posterior to the glenoid fossa.

The broadened anterior tips of the premaxillaries protrude anteriorly from below the anterior ends of the dentaries. This condition is typical of Dinocephalosaurus orientalis among archosauromorphs, and can also be observed in the holotype skull. The right premaxilla shows that the fourth premaxillary tooth formed the enlarged premaxillary fang, as was also inferred to be the case in the holotype (Rieppel et al. Reference Rieppel, Li and Fraser2008). On both sides, two enlarged maxillary fangs protrude from below the mandibular rami, separated from the premaxillary fang by a series of smaller teeth, the number of which cannot unequivocally be established. Indeed, the difficulty in unequivocally identifying maxillary versus dentary teeth, more numerously exposed on the right than on the left side, renders a precise tooth count for these two elements impossible. Those teeth lying immediately behind the right premaxillary fang belong to a well-defined series of anterior dentary teeth, which indicates the possible existence of a diastema in the upper jaw tooth row separating the premaxillary from the maxillary dentition. In the holotype skull, this diastema appears to accommodate two, possibly three, dentary teeth.

2.3.3. The vertebrae

The series of vertebrae are preserved with their right lateral sides exposed. The first nine elements are preserved in almost perfect articulation and even the cervical ribs are paired in relatively close association with their respective vertebrae, although they are splayed ventrally away from the long axis of the neck. There is then a short gap in the slab that accounts for the posterior part of the ninth vertebra together with all of the tenth vertebra. Vertebrae 11 to 17 are also preserved in perfect articulation with each other and their respective ribs. Each rib has a very distinctive anterior process that extends beyond the separate capitulum and tuberculum. In lateral view this anterior process has a distinct excavation on its dorsal edge just in front of the capitulum. The process then broadens out slightly before tapering again towards its anterior tip. This depression corresponds exactly to the position of the posterior edge of the preceding centrum and it seems likely that in life it formed a direct articulation with the centrum. If this was the case it might have permitted a certain degree of dorsiflexion of the neck. The relative length of the anterior process of the ribs is comparable to that seen in Sclerostropheus fossai, Tanytrachelos ahynis and Pectodens zhenyuensis among tanystropheids and dinocephalosaurids (Olsen Reference Olsen1979; Li et al. Reference Li, Rieppel and Fraser2017b; Spiekman & Scheyer Reference Spiekman and Scheyer2019) and also similar to that seen in the putative early archosauromorph Czatkowiella harae (Borsuk-Białynicka & Evans Reference Borsuk-Białynicka and Evans2009), and considerably longer than that seen in other early archosauromorphs. The ribs on the first nine or ten vertebrae are almost entirely straight. But from cervical 11 onwards the ribs assume a very gentle uniform curvature. None exhibit the slight kinks described in the cervical ribs of a specimen of Tanystropheus (Rieppel et al. Reference Rieppel, Jiang, Fraser, Hao, Motani, Sun and Sun2010) where they extended across the intervertebral joints.

2.4.1. The skull and dentary

In the exploded skull the well-preserved right premaxilla (Fig. 5a) is exposed in medial view. The alveolar margin of the body of the premaxilla carries five identifiable tooth positions, of which the anteriormost and posteriormost ones are empty. The slender, tapering nasal process (prenarial process) of the premaxilla extends posterodorsally; its length is about twice that of the body of the premaxilla. This process would have separated the two external nares from each other, as is the case in most non-archosauriform archosauromorphs, except for Tanystropheus spp., certain allokotosaurs (e.g., Shringasaurus indicus, Azendohsaurus madagaskarensis, Pamelaria dolichotrachela), rhynchosaurs and Teyujagua paradoxa, in which the external nares are confluent (Dilkes Reference Dilkes1998; Flynn et al. Reference Flynn, Nesbitt, Michael Parrish, Ranivoharimanana and Wyss2010; Pinheiro et al. Reference Pinheiro, Simão-Oliveira and Butler2019; Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020a, Reference Spiekman, Fraser and Scheyer2021). The process directed posteriorly from the main body of the premaxilla (postnarial process) is strongly reduced in Dinocephalosaurus orientalis and tapers posterodorsally. Three premaxillary teeth are preserved in the second to the fourth tooth positions. Tooth implantation (sensu Ezcurra Reference Ezcurra2016) is subthecodont. The third and fourth teeth are equal in length while distinctly longer than the second tooth. The teeth are pointed and recurved, and the enamel surface is distinctly striated in the apical part. Resorption pits are located on the labial side of the tooth base, with a replacement tooth located inside its pit at the base of the third premaxillary tooth.

Figure 5 Dinocephalosaurus orientalis, ZMNH M8727, interpretative drawings of selected cranial remains. (a) Premaxilla, dentary and mandibular condyle of quadrate. (b) Right maxilla in medial view. (c) Left pterygoid in ventral view. (d) Right (?) quadrate in medial (?) view. Abbreviations: as.p = ascending process of the maxilla; d = dentary; np.pm = nasal process of the premaxilla; pl.p.pt = palatine process of the pterygoid; pm = premaxilla; pm.f = premaxillary process of the maxilla; q.cph.c = cephalic condyle of the quadrate; q.md.c = medial condyle of the quadrate; q.p.pt = quadrate process of the pterygoid; sym = symphysis; tr.p.pt = transverse process of the pterygoid.

Located behind the right premaxilla lies the right maxilla, which is also exposed in medial view (Fig. 5b). The maxilla carries a rather slender anterior process that projects beyond the anteriormost preserved tooth, and that ends in a blunt tip. Its dorsal margin would seem to have defined the lateral margin of the external naris that was located within the antorbital recess. The ascending (facial) process of the maxilla ascends rather abruptly at what appears to have been the level of the posterior margin of the external naris. From there, the dorsal margin of the ascending process gently curves posterodorsally, the maxilla thus gaining in height. The ascending process is damaged (incomplete) in its posterior part, which does not allow us to ascertain whether it defined the anterior margin of the orbit, or whether a lacrimal was present. Although again incomplete at its posterior end, the maxilla does show a tapering, tooth-bearing suborbital process extending posteriorly below the anterior part of the orbit, as is also seen in the skull of the holotype.

The holotype skull (Fig. 1) shows a minimum of three maxillary teeth preceding the paired maxillary fangs, and the same is observed in ZMNH M8727. If this is indeed the natural condition, the anterior process of the maxilla, lining the external naris laterally, would be edentulous and the premaxillary and maxillary tooth row would thus be separated by a diastema that accommodates anterior dentary teeth. The total number of teeth preserved on the left maxilla amounts to 13, to which may be added four, possibly five, empty tooth positions (the posterior tip of the maxilla is missing). Tooth implantation is thecodont (sensu Ezcurra Reference Ezcurra2016). The relatively long anterior maxillary teeth are distinctly recurved, the shorter posterior maxillary teeth are straight. All teeth are pointed, the enamel covering distinctly striated towards the apex of the crown. The base of the teeth reveals deep striations that appear to result from infolding, thus revealing the presence of plicidentine in Dinocephalosaurus orientalis. Plicidentine has previously not been established in any archosauromorph reptile, but is known to occur in ichthyosaurs, choristoderes, squamates and possibly sauropterygians among diapsids (Maxwell et al. Reference Maxwell, Caldwell and Lamoureux2011; Spiekman & Klein Reference Spiekman and Klein2021). The morphology of the tooth crowns is very similar to that seen in Tanystropheus hydroides (Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b). This taxon similarly possesses fang-like, striated maxillary teeth that are heterogeneous in size. In Tanystropheus hydroides, the maxillary teeth increase in size until tooth position seven, after which the size of the teeth gradually decreases until the 15th and terminal tooth position. However, in contrast to Dinocephalosaurus orientalis, tooth implantation in the maxilla of Tanystropheus hydroides is distinctly subthecodont and there is no plicidentine infolding at the tooth roots.

The parietal skull table is preserved in ventral view, pierced by the relatively large pineal foramen located well within the parietal. The posterolateral (supratemporal) processes of the parietal are incomplete, however. The irregularly shaped, but essentially triradiate element located next to the parietal skull table most likely represents a damaged, or incompletely exposed postorbital.

The left pterygoid is well exposed in ventral view (Fig. 5c). It shows the large, broad, plate-like palatal ramus, which, as mentioned above, is similar in outline to that of Tanystropheus hydroides (Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b), and which dominates the formation of the nearly closed dermal palate. The transverse posterior margin that defines the anterior margin of the subtemporal fenestra is nearly straight. The relatively slender quadrate ramus of the pterygoid curves posterolaterally, forming a concave lateral margin. A distinct notch on the medial margin of the pterygoid, located at the juncture of the palatine and quadrate rami, marks the location of the palatobasal articulation. The anterior end of the palatal ramus of the left pterygoid is crossed over by the anterior end of the incompletely preserved palatal ramus of the right pterygoid, its posterior end broken.

Two ossifications are identifiable as representing the quadrates (Fig. 4b). One is located next to the disarticulated right dentary. It is a relatively small ossification of irregular pentagonal shape, its smoothly convex ventral margin forming the mandibular condyle. The other quadrate lies at some distance from the posterior end of the left pterygoid, again showing the same convex configuration of the mandibular condyle. In contrast to the (presumably) right quadrate, the (presumably) left quadrate is dorsally broadly expanded (Fig. 5d). It lacks the hook-shaped posterior end of the dorsal head seen in Tanystropheus hydroides, Tanystropheus longobardicus and allokotosaurs (Flynn et al. Reference Flynn, Nesbitt, Michael Parrish, Ranivoharimanana and Wyss2010; Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b, Reference Spiekman, Fraser and Scheyer2021; Sengupta & Bandyopadhyay Reference Sengupta and Bandyopadhyay2022). The posterior margin is distinctly concave due to a posterodorsal expansion that terminates in a pointed tip. Much more expansive is an anterodorsal, deep and flange-like expansion, forming what looks like an anterodorsal wing of the quadrate. By comparison to the holotype skull, it appears that the (presumably) left quadrate is associated with incomplete remains of the squamosal.

The right dentary is beautifully exposed in medial view (Fig. 5a). It is a slender element that is expanded at its anterior tip, forming a somewhat fortified mandibular symphysis, which is similar to the condition seen in Tanystropheus hydroides, albeit less strongly developed (Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b). A distinct alveolar shelf overhangs Meckel's canal and carries the dentary teeth. Posteriorly, the dentary gains somewhat in depth, terminating in an indented convex margin. The indentations most probably accommodated the anterior tip of the surangular. A total of 13 complete teeth are preserved on the dentary, an incomplete number. The complete tooth count is difficult to estimate, but could comprise as many as 20 to 21 teeth. Tooth implantation is thecodont (sensu Ezcurra Reference Ezcurra2016). The teeth are pointed, covered with striated enamel apically, and showing indications of resorption pits and plicidentine infolding on the lingual aspect of the tooth base. The anteriormost preserved dentary tooth is distinctly recurved, but more anteriorly than in the upper tooth row the dentary teeth subsequently become upright.

2.4.2. The vertebral column

(Table 1). Two kidney-shaped ossifications located in front of the axis could represent the atlas neural arches. The axis is disarticulated but aligned with the cervical series behind it and it is beautifully exposed in left lateral view (Fig. 6a). It is distinctly shorter than the third and subsequent cervical vertebrae. The ventral margin of the centrum is strongly concave in lateral view. At the anterior end of the centrum the pedicel of the neural arch contributes to the formation of a short yet distinct transverse process that supported the cervical rib (not preserved). The neurocentral suture is fused. The prezygapophysis is damaged (incomplete), but the postzygapophysis is distinct and bears a well-developed epipophysis dorsally. Between the pre- and postzygapophyses the neural arch shows a slight elevation with a weakly convex dorsal margin, which is all there is in terms of a rudimentary neural spine, or rather neural crest. Thus, Dinocephalosaurus orientalis lacks the anterodorsal expansion of the axial neural spine seen in tanystropheids (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021).

Table 1 Length and height of the cervical vertebrae, specimens ZMNH M8727, IVPP V13898, IVPP V0666, and ZMNH M8752. Abbreviation: CV = cervical vertebra. The length was measured across the ventral margin of the centrum; the height was measured across mid-centrum and includes the neural crest. All measurements are in mm. The measurements of ZMNH M8752 are approximate only, which is due to the tight articulation between vertebrae, as well as to the cervical ribs often obscuring the ventral margin of the centrum. Superscripts: 1 = estimate; 2 = incomplete element; 3 = element is missing part of the centrum, but the ventral limit of the bone can be accurately measured from the impression of the bone in the matrix; 4 = includes a fine crack running through the element; 5 = element partially crushed and distorted; 6 = element minimally obscured along the margin; 7 = unclear where the articulation between the centra lies. Combined length of centra 25 + 26 is 189.

Figure 6 Dinocephalosaurus orientalis, ZMNH M8727, interpretative drawings of selected postcranial elements. (a) Axis in left lateral view. (b) Sixth cervical vertebra in left lateral view. (c) Posterior cervical vertebra (between 18th and 24th) in right lateral view. (d) Anterior dorsal vertebra in anterior view. (e) Right scapula in medial view. (f) Both coracoids, right coracoid in medial view and left coracoid in lateral view. Abbreviations: c = centrum; co.dex = right coracoid; co.sin = left coracoid; gl.f = glenoid facet; ncr = neural crest; poz = postzygapophysis; prz = prezygapophysis; sc = scapula blade; tr.p = transverse process.

Behind the axis, the third through to the 18th cervical vertebrae are preserved in an undisturbed, articulated string of vertebrae that is bent backwards. The morphology of the cervical vertebrae is generally very similar throughout this section of the neck (Fig. 6b, c). The vertebrae are distinctly elongated, increasing in length all the way up to the 18th cervical vertebra, the last one preserved in articulation. The ventral margin of the centrum is distinctly concave in lateral view, similar to that seen in Augustaburiania vatagini (Sennikov Reference Sennikov2011). The articular facets for the cervical ribs are located closely together, low on the centrum near its anterior margin. The neurocentral suture is obliterated. The postzygapophysis is slender and underlain by the more massively built prezygapophysis, the latter terminating in a deep, rounded (anteriorly convex) tip. Dorsal to the postzygapophysis, a pronounced, slender and lateromedially narrow epipophysis is present, which extends posteriorly beyond the articular facet of postzygapophysis, as in the long-necked tanystropheids Tanystropheus spp., Amotosaurus rotfeldensis, Raibliania calligarisi, Augustaburiania vatagini and Fuyuansaurus acutirostris (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). The neural spine is represented by a low neural crest with a weakly concave dorsal margin that dorsally expands between the pre- and postzygapophysis, which is similar to the condition seen in Amotosaurus rotfeldensis and Augustaburiania vatagini (Fraser & Rieppel Reference Fraser and Rieppel2006; Sennikov Reference Sennikov2011). The cervical neural spines do not bear mammillary processes, nor are they transversely expanded distally to form a spine table, in contrast to several archosauromorph taxa, including certain tanystropheids (Pritchard et al. Reference Pritchard, Turner, Nesbitt, Irmis and Smith2015; Ezcurra Reference Ezcurra2016; Scheyer et al. Reference Scheyer, Wang, Li, Miedema and Spiekman2020; Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). Generally, this neural crest becomes progressively more distinctly developed in an antero-posterior gradation within this articulated series of cervical vertebrae.

Behind the series of 18 articulated cervical vertebrae a set of six partially or fully disarticulated cervical vertebrae is located, which retain the distinctly elongated morphology. Of these, four elements continue the string of the 18 articulated elements across an area damaged by breakage. Two elements are fully disarticulated and oriented at an angle relative to the long axis of the articulated cervical column. Within this set of six cervical vertebrae, an increasingly more prominent development of the neural crest is the only distinctive feature that distinguishes them from more anterior cervical vertebrae. The neural crest is most prominently developed in a vertebra that is fully disarticulated and dislocated, lying somewhat to the side with its postzygapophysis pointing in an anterior direction relative to the whole skeleton. By virtue of its well-developed neural crest, this element is identified as the 24th cervical (Fig. 6c). The 25th to the 28th cervical vertebrae again form an articulated series, preserved in reverse orientation relative to the anterior series of the 18 articulated cervical vertebrae. The 28th cervical is incompletely preserved, whereas the neural crest on the 27th cervical is either incompletely preserved or incompletely exposed. The 25th and 26th cervical vertebrae document a further elaboration of the neural crest, which gains in height particularly in its posterior part, and acquires a more pronounced convex dorsal margin.

With reference to other specimens of Dinocephalosaurus orientalis to be described below, more posterior cervical vertebrae are known to be much shorter in length compared to the preceding cervical vertebrae and to approach the morphology of anterior dorsal elements. A string of nine shortened but otherwise incompletely exposed posterior cervical vertebrae and/or anterior dorsal vertebrae lies in front of the preserved elements of the pectoral girdle. On the basis of associated relatively short posterior cervical ribs, four out of the string of nine vertebrae in front of the elements of the pectoral girdle are identified as shortened posterior cervical vertebrae. The next element in the series is overlain by a dorsal rib, which might have been associated with it. It is therefore counted as one out of five anterior dorsal vertebrae preserved in the series. Including the atlas and the axis, the vertebral count for the cervical region is thus a string of 18 fully articulated elements that includes the atlas and axis, two dislocated elongated elements, another section of four articulated elongated elements of which the last one is the 28th cervical, and a minimum of four shortened, posteriormost cervical vertebrae, which amounts to a total of 32 cervical vertebrae.

The cervical ribs are typical of non-crocopodan archosauromorphs, much elongated and aligned parallel to the ventrolateral margin of the cervical series of vertebrae. A distinct, free-ending anterior process projects beyond the articular head of the rib. The latter is oriented at a right angle to the shaft of the rib and articulates on a facet located low on the centrum near the latter's anterior margin. As preserved, the cervical ribs are deflected away from the posteriorly bent neck (Fig. 4). In their natural orientation, ribs associated with the fourth cervical vertebra would have bridged three successive intervertebral joints; the rib associated with the eighth cervical would have bridged five successive intervertebral joints; the rib associated with the 13th cervical would also have bridged five succeeding intervertebral joints. Cervical ribs extend the length of two or more cervical vertebrae in Protorosaurus speneri, Pectodens zhenyuensis and most tanystropheids, except for Tanytrachelos ahynis and Langobardisaurus pandolfii, which have relatively shorter cervical ribs (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). In the posterior part of the cervical vertebral column, where the vertebrae become shorter, the cervical ribs likewise become shorter, and at the same time more massively built, as is also the case in tanystropheids.

Partially overlapping the laterodorsal aspect of the (articulated) 18th cervical is a disarticulated anterior dorsal vertebra that is beautifully exposed in anterior view (Fig. 6d). The entire height of the element, from the ventral margin of the centrum to the tip of the neural spine, is 73.1 mm; the total width across the transverse processes is 85 mm. The height of the centrum alone is 34.7 mm and its width is 33.9 mm. The articular surface of the centrum is of rounded circumference, amphicoelous, and the centrum is non-notochordal. The neural canal is of rectangular contours, the massive prezygapophyses projecting from its dorsal margin. A distinct neural spine, which is not transversely expanded distally, rises up from the neural arch behind the prezygapophyses. Laterally, the neural arch is developed into deep transverse processes. Their tall distal articular surface faces ventrolaterally. In Dinocephalosaurus orientalis, the transverse processes of the posteriormost cervical vertebrae and anterior dorsal vertebrae are very distinctively differentiated in that their anterior surface is deeply excavated (concave) and their posterior surface correspondingly convex in lateral view (see below). The dorsal surface is flat, the anterodorsal margin forming an overhanging shelf. A second anterior dorsal is incompletely exposed in the area between the 18th and 27th cervical.

A number of disarticulated dorsal ribs are preserved, scattered across the specimen (Fig. 4). They are evenly curved and show a slight distal expansion. Their proximal articular head is distinctly expanded to match the articular surface on the tall transverse process of the dorsal vertebrae. In addition to the cervical and dorsal ribs, scattered gastral ribs are likewise preserved. Generally slender and of delicate structure, they display two different morphologies. The medioventrally located elements are slightly angulated and taper to a fine tip on both sides. The collateral elements are weakly but evenly curved, terminating in a blunt tip proximally and in a finely pointed tip distally. Although disarticulated, the dense accumulation of gastralia suggests they formed a tightly bundled gastral basket.

2.4.3. The pectoral girdle and forelimb

Of the elements of the pectoral girdle, both coracoids are preserved lying next to one another (Fig. 6f). They form kidney-shaped plate-like elements 77 mm long (left coracoid) and 51 mm deep (right coracoid). A well-demarcated peduncle carries the ventral part of the glenoid facet. The coracoid foramen is located below and somewhat in front of this glenoid ‘process’. The right scapula is dislocated but fully exposed (Fig. 6e). Again, a kidney-shaped plate-like element 98 mm long and 63.5 mm deep, it carries a glenoid ‘peduncle’ or ‘process’ that, together with its counterpart on the coracoid, completes the glenoid facet. A kidney-shaped scapula with a semicircular scapular blade is typical of Dinocephalosaurus orientalis, Pectodens zhenyuensis and tanystropheids among archosauromorphs (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021), and it is absent in other archosauromorphs, including the non-crocopodans Protorosaurus speneri and Prolacerta broomi (Gottmann-Quesada & Sander Reference Gottmann-Quesada and Sander2009; Spiekman Reference Spiekman2018). The shape of the anterior margins of both the scapula and coracoid suggests that a scapulocoracoidal fenestra, as is present in tanystropheids, is absent in Dinocephalosaurus orientalis. This observation is corroborated in IVPP V20295, which preserves an articulated scapulacoracoid (see below). The left scapula is only partially exposed, but its posteroventral portion protrudes from below the left coracoid. The anterior part is developed into a broad plate, the exact contours of which remain concealed by the overlapping coracoid. Posteriorly, the element appears to extend into a robust posterior stem that tapers to a blunt tip. A broken curved ossification located near the left coracoid could represent an incomplete clavicle, but it could also be a fragment of a dorsal rib.

Both the left and the right humeri are well preserved and exposed (Fig. 4). They are slightly curved elements which, due to skeletal paedomorphosis, show little morphological differentiation. An entepicondylar foramen is absent. The ectepicondylar groove is shallow, with a weakly expressed ectepicondylar notch at its distal end. Only a fragment of the distal end of the left radius is preserved. Of the left ulna, only the distinctly expanded proximal part is exposed. The right zeugopodium is more completely preserved and exposed, although overlying ribs again obscure parts of the elements. The proximal end of the ulna is more distinctly expanded than that of the radius, whereas distally the radius is more massively built than the ulna. A total of seven rounded carpal ossifications are scattered across the slab distal to the stylopodial and zeugopodial elements, as are five, possibly six, metacarpals and a number of phalanges (Fig. 4). These autopodial elements evidently derive from both hands. Their disarticulation and incompleteness do not allow a reconstruction of the structure of the manus.

2.5.1. The skull and mandible

The incompletely preserved right side of the skull and the right mandible are preserved in articulation. The body of the right premaxilla shows five tooth positions with the first four teeth preserved in situ and the fifth tooth being broken. The third premaxillary tooth is the largest, given that the fourth tooth position shows an erupting replacement tooth. The tooth crown is recurved and pointed, covered by striated enamel towards the apex. Behind the premaxilla extends a strip of bone that represents the partially preserved and exposed maxilla; the maxillary tooth row is not preserved or exposed, except for two alveolar sockets located at the level of the anterior margin of the orbit. A gap located behind the body of the premaxilla, separating the preserved/exposed part of the maxilla from a sheet of bone that represents the nasal, most probably corresponds to the antorbital recess. Posterior to the maxilla and nasal lies a well-defined, vertically oriented, semi-lunar prefrontal with a strongly convex anterior margin, and a concave posterior margin that defines the anterior margin of the orbit, which is typical of early archosauromorphs, including tanystropheids (e.g., Flynn et al. Reference Flynn, Nesbitt, Michael Parrish, Ranivoharimanana and Wyss2010; Miedema et al. Reference Miedema, Spiekman, Fernandez, Reumer and Scheyer2020; Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b). Crushed and distorted parts of the parietal skull table, involving the frontal and parietal, are exposed at the dorsal margin of the skull above the orbital and temporal region. Crushed bone fragments, which are posterodorsally located and offer no anatomical detail, most probably represent remains of the braincase. The right pterygoid is very well preserved (Fig. 8b) and exposed below the posterior part of the maxilla, the orbit and the temporal region. The palatine ramus of the pterygoid can be seen reaching far forward to a level well in front of the prefrontal, although its further anterior extent disappears below the remains of the maxilla. The prominent and rounded transverse process is deflected ventrally as a consequence of distortion, and exhibits a strongly rugose lateral surface, which is similar to that seen in Tanystropheus hydroides (Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b). The quadrate process of the pterygoid is revealed to be rather deep in lateral view. It terminates in a tall posterior edge that has separated from the crushed quadrate lying behind it. Within the area of the orbit, behind the posterior end of the exposed part of the maxilla and located right at the base of the palatine ramus of the pterygoid, lie a couple of trapezoid-shaped ossifications, their lateral margins slightly convex. Given their intact preservation and location, these elements are identified as ectopterygoids.

Figure 8 Dinocephalosaurus orientalis, ZMNH M8728, interpretative drawings of selected elements. (a) Right mandibular ramus in lateral view. (b) Right pterygoid in lateral view. (c) Posterior cervical vertebrae and anteriormost dorsal vertebra (cv26–do.v1) in right lateral view. (d) Mid-dorsal vertebrae in right lateral view. (e) Right forelimb, as preserved. (f) Left forelimb, as preserved. Abbreviations: ang = angular; ar = articular; c = centrum; cv = cervical vertebra; d = dentary; dc = distal carpal; do.v = dorsal vertebra; hu = humerus; int = intermedium; mc = metacarpal; ncr = neural crest; ns = neural spine; pl.p.pt = palatine process of the pterygoid; poz = postzygapophysis; prz = prezygapophysis; q.p.pt = quadrate process of the pterygoid; sang = surangular; sym = symphysis; tr.p = transverse process; tr.p.pt = transverse process of the pterygoid; ra = radius; rad = radiale; ul = ulna; uln = ulnare.

The right mandibular ramus is preserved in right lateral view (Fig. 8a); from below it emerges the lower margin of the left mandibular ramus, with the left dentary sheared off and exposed ventrally. The anterior tip of the dentary is slightly broadened to form a fortified mandibular symphysis. The largest dentary teeth, four in number, follow two or three much smaller anterior dentary teeth. The four enlarged dentary teeth would thus come to lie in between the premaxillary and the maxillary fangs. The dentary tooth row is not completely preserved, but with 14 complete and incomplete dentary teeth preserved in situ, a total of 19–21 tooth positions can be assumed. While the enlarged anterior dentary teeth are still somewhat recurved, those located behind them are straight upright. Again, the dentary teeth are pointed, their enamel covering striated towards the apex of the crown. Some of the more posteriorly located dentary teeth show plicidentine infolding at their base. If any coronoid process were developed it could form a weak elevation only, obscured by the overlapping transverse process of the pterygoid. A retroarticular process is again confirmed to be reduced in size. Sutural details are hardly identifiable except for the partial posterior delimitation of the dentary. What looks like a sinuously curved crack in the postdentary part of the mandible might represent the natural separation of the dorsally located surangular from the ventrally located angular.

2.5.2. The vertebral column

(Table 2). The atlas is not identifiable and the axis is only partially exposed, crushed between the posterior end of the right mandibular ramus and bone fragments that most probably represent remnants of the braincase. But from the third cervical vertebra on backwards, the entire cervical and most of the dorsal region is beautifully preserved in articulation (with a break between cervical 23 and cervical 24), and exposed in right lateral view (Fig. 7). Cervical vertebrae 3 through to 28 show the elongated morphology also characteristic of the other specimens of Dinocephalosaurus orientalis. The length of the centrum increases steadily from cervical vertebra 3 to cervical vertebra 23, behind which it decreases again more rapidly. Up to cervical vertebra 24, the ventral margin of the centrum is strongly concave in lateral view, which gives the impression of a markedly expanded anterior and posterior intervertebral articular facet. The articular facets for the cervical ribs lie low on the centrum near its anterior margin. The prezygapophysis is again shorter and more massively built than the postzygapophyses, the latter bearing prominent epipophyses that extend beyond the posterior margin of the centrum as it tapers to a pointed tip. Up to cervical vertebra 24, the neural crest is extremely shallow, its concave dorsal margin resulting in weakly expressed anterior and posterior dorsal projections located between the pre- and postzygapophyses respectively. The neurocentral suture is fused; there is no indication that the vertebral centra would be hollow, as they are in Tanystropheus (Wild Reference Wild1973; Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b).

Table 2 Length and height of the presacral vertebrae, specimens IVPP V20295 and ZMNH M8728. Abbreviations: CV = cervical vertebra; PSV = presacral vertebra. The length was measured across the ventral margin of the centrum; the height was measured across mid-centrum and includes the neural crest. All measurements are in mm. Superscripts: 1 = not completely exposed; 2 = dorsals 5 and 6 are slightly distorted; 3 = element marginally obscured; 4 = approximate length as the element is broken.

A transition in the morphology of the cervical vertebrae starts with cervical 26 (Fig. 8c). Somewhat shorter already (see Table 5), the vertebra gains in depth, the ventral margin of the centrum being less concave in lateral view, the neural crest more prominently developed and with a straight dorsal margin. Posteriorly, the neural crest develops into a posterior projection that overhangs the zygapophyseal articulation. Pre- and postzygapophyses are more symmetrically developed, projecting less beyond the anterior and posterior margins of the centrum than in more anteriorly located cervical vertebrae. In cervical vertebra 27, the same trend of morphological transformation continues, culminating in cervical vertebra 28, which again has diminished in length compared to the directly preceding vertebrae. The central margin of the centrum is only slightly concave in lateral view; the neural crest is rather prominently developed with a distinctly convexdorsal margin, and it carries a posterior projection that extends well beyond the zygapophyseal articulation. In addition, the diapophysis, which in preceding cervical vertebrae was positioned directly adjacent to the parapophysis near the anteroventral end of the centrum, has shifted dorsally onto about the mid-height of the centrum.

Further modifications occur in more posterior cervical vertebrae as these lead up to the anterior dorsal vertebrae (Fig. 8c). The length of the centrum decreases rapidly, whereas its depth increases, such that the centrum of cervical vertebra 32 has acquired the proportions characteristic of dorsal vertebrae. The ventral margin of the centrum becomes more pronouncedly concave again in lateral view. The articular facets for the cervical rib are increased (to match the size of the articular heads of the short and more massively built cervical rib), with the diapophysis being positioned further dorsally, possibly being placed partially on the neural arch, and a laterally projecting crest develops that runs from the diapophysis backwards along the length of the centrum. Pre-and postzygapophyses are symmetrically developed, and between them rises up a prominent yet slender, curved, finger-like neural spine pointing posterodorsally, which is a morphology that is apparently unique among early archosauromorphs. The 32rd presacral vertebra can be identified as a cervical based on its position distinctly anterior to the pectoral and its short associated rib that is oriented mostly posterior and slightly ventral to the vertebral column (i.e., a rib that therefore does not contribute to the rib cage of the trunk). The 36th presacral vertebra can be identified as a dorsal element, as it is associated with a dorsal rib (i.e., a rib that curves ventrolaterally from its head to contribute to the rib cage). The 33rd presacral vertebra has only a partial rib associated with it, whereas no ribs are preserved in association with the 34th and 35th presacral vertebrae, and these elements might be considered transitional elements.

The anterior cervical ribs are much elongated, their shaft aligned along the long axis of the cervical vertebral column (Fig. 7). The rectangular articular heads, which are set parallel to each other, are oriented at a right angle relative to the long axis of the shaft, and the cervical rib terminates anteriorly in an elongate free-ending, anterior process. The ribs associated with cervical vertebrae 3 and 4 are clearly identifiable, which leaves the shafts of a total of four cervical ribs bridging the intervertebral joint between axis and cervical 3. This confirms that the first pair of cervical ribs articulated on the atlas. It is noteworthy that the shaft of these anteriormost cervical ribs is much elongated already, as its posterior tip lies behind the intervertebral joint between cervical 3 and 4. Towards the middle and more posterior parts of the neck, cervical ribs may bridge up to five or six intervertebral joints. The last of these slender, much elongated cervical ribs, articulating with cervical vertebra 27 and – possibly – cervical vertebra 28, terminate posteriorly just in front of, or below, cervical vertebra 32 and the first dorsal vertebra. Starting with cervical vertebra 29, the cervical ribs undergo a characteristic modification, which also occurs in other long-necked archosauromorphs like Tanystropheus spp. and Tanytrachelos ahynis (Olsen Reference Olsen1979; Rieppel et al. Reference Rieppel, Jiang, Fraser, Hao, Motani, Sun and Sun2010): they become much more robustly built and shorter. The articular head increases in relative size, as does the free-ending anterior process, while the posteriorly extending shaft is short, distinctly curved, and terminating in a pointed tip.

A string of 21 dorsal vertebrae is preserved, the last one in the series only incompletely so. The centra of the dorsal vertebrae are both laterally and ventrally strongly constricted (Fig. 8d). The neural arch of the dorsal vertebrae is very robust, being in that regard more similar to that seen in sauropterygians than that of archosauromorphs (Rieppel Reference Rieppel2000; Ezcurra Reference Ezcurra2016; Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). Pre- and postzygapophyses are symmetrically differentiated and do not project far beyond the anterior and posterior margins of the centrum. The well-developed transverse processes are of a rather peculiar morphology: they are very tall in their dorso-ventral dimension, but slender in their antero-posterior dimension. Their anterior surface is deeply excavated or concave, which translates into a prominently convex posterior surface. As was described above, cervical vertebrae 29 through to 32 develop a prominent neural spine that forms a slender, posterodorsally curving projection. With presacral vertebra 33 begins a reduction in the relative size of the neural spine that continues through to the 40th and 41st presacral vertebra. Further posteriorly, the development of the neural spine becomes more prominent again, now assuming rectangular contours in lateral view. Their anterior and posterior margin is slightly concave in lateral view, whereas their dorsal margin is either straight or slightly convex. The dorsal ribs are evenly curved and show a slight distal expansion. Their proximal articular head is much expanded into a triangular structure that matches the height of the transverse processes.

The gastral rib basket is well preserved, albeit mostly disarticulated (Fig. 7). Some of the gastral ribs retain their natural configuration, however, showing that each gastral rib is composed of three elements, an angulated medioventral one, the apex pointing forwards, and one collateral element on either side, forming an overlapping contact. The collateral elements are slender, pointed at both ends, and weakly curved dorsally in their lateral part. The gastral basket was clearly tightly bunched.

2.5.3. The pectoral girdle and forelimb

Despite the pectoral girdle of ZMNH M8728 being otherwise complete and the entire skeleton being largely in articulation, an interclavicle is not preserved, nor is it in any other known specimen of Dinocephalosaurus orientalis. This suggests that an ossified interclavicle was probably absent in this taxon, as is also the case in Tanystropheus spp. and Ozimek volans (Spiekman et al. Reference Spiekman, Fraser and Scheyer2021). The right clavicle is broken across the transition from the cervical to the dorsal vertebral column. The anterior (medial) part of the left clavicle protrudes from below the right scapula (Fig. 7). The clavicle is an evenly curved, blade-like element, with its anterior (medial) end slightly set off by a weak constriction. The right scapulocoracoid is well preserved and exposed in articulation; it overlaps, and thus partly obscures, the left scapulocoracoid. The right coracoid forms a kidney-shaped element with the dorsal ‘glenoid process’ located in its posterodorsal part. The coracoid foramen is located just anteroventral to this ‘glenoid process’, and it is fully enclosed by bone. The length of the coracoid is 93 mm and its depth is 47 mm. The scapula again forms a kidney-shaped element with a ‘glenoid process’ located at its anterior end, which together with its counterpart from the coracoid completes the glenoid facet. The length of the right scapula is about 82 mm and its depth is 67.8 mm.

The right humerus is well preserved and exposed (Figs 7, 8e); the distal end of the left humerus protrudes from below the two coracoids and passes below the distal end of the right humerus. In ZMNH M8728, the (right) humerus is a rather straight element, unlike in ZMNH M8727, where it appears curved. Possibly, this is the result of the angle under which the elements are exposed, which cannot be discerned confidently due to the lack of observable features (attributable to paedomorphosis). Its proximal and distal ends are expanded, which results in a biconcave shaft. Little morphological detail is differentiated or identifiable. An entepicondylar foramen is absent. The ectepicondylar groove and (distal) notch are weakly expressed. Both the right and the left zeugopodium are well preserved and exposed (Fig. 8e, f). The radius and ulna are subequal in length, the ulna being just a bit shorter than the radius (see Table 3). The radius is a bit more robustly built than the ulna. It is expanded proximally as well as distally to a similar degree, which results in a biconcave shaft. The concavity of the postaxial margin of the shaft, defining the spatium interosseum, is more pronounced than the concavity of the preaxial margin of the shaft. The ulna is markedly expanded proximally but only weakly expanded distally. An ossified olecranon is absent. The preaxial margin, defining the spatium interosseum, is concave; its preaxial margin is rather straight instead, with a weak concavity expressed at the distal end.

Table 3 Length and width of the individual forelimb elements in the four specimens preserving the forelimbs, ZMNH M8727, ZMNH M8728, ZMNH M8752 and IVPP V20295. Abbreviations: L = length; PW = proximal width; MW = minimal width; DW = distal width. All measurements are in mm.

Five carpal ossifications are preserved in the right manus (Fig. 8e) and six in the left autopodium (Fig. 8f). In both hands, there are three proximal carpal ossifications, and two versus three distal carpal ossifications, respectively. In the right manus, the irregularly polygonically shaped proximal carpals are preserved in articulation (sutural contact) and comprise the radiale (maximum exposed length: left, 19.2 mm; right, 19.6 mm), intermedium (left, 21 mm; right, 20.7 mm) and ulnare (left, 13,6 mm; right, 15.2 mm). Of those, the intermedium is the largest and the ulnare the smallest. In the distal carpal row of the right hand, a distinctly larger element lies in a preaxial position relative to the smaller distal carpal located postaxially. The same two distal carpals of similar relative size can be identified in the left manus, where the larger preaxially located element lies proximal to metacarpal II. The somewhat smaller postaxially located element is situated proximal to metacarpal IV, albeit a bit removed from it. A much smaller third distal carpal is located in between the two aforementioned elements, situated proximal to metacarpal III. This latter element has been lost or failed to ossify in the right manus. In ZMNH M8728, there are thus three distal carpals ossified, of which dcII is the largest, dcIII the smallest, and dcIV is intermediate in size.

Of the five metacarpals (Fig. 8e, f), the first through to the fourth are relatively elongated, slender elements with a biconcave shaft. Amongst them, the third and the fourth are the longest. The fifth metacarpal is distinctly shorter, approximately of the same length as the first metacarpal, but more sturdily built. The phalangeal count is 1–2–4–5–1 in both hands and only the digits III and IV terminate in an element that is clearly identifiable as an ungual. It thus appears that the more distal phalanges in digits I, II and V were absent or did not ossify. There is no indication of a juvenile status of this specimen, since it is of respectable adult size, and this limited phalangeal count probably represents a paedomorphism related to aquatic adaptation.

2.6.1. The skull and mandible

The skull and mandible are preserved in articulation and exposed in left lateral view. Preservation is such, however, that little anatomical detail is discernible. The tip of the snout is deflected to the left so as to expose the premaxillae in anterior view. As a consequence, a left and a right premaxillary fang embrace the tip of the left mandible. On the dorsal surface of the rostrum, the anterior end of the antorbital recess is particularly well exposed on the left side, lined medially by the very elongate posterior (nasal) process of the premaxilla. The remainder of the skull is preserved as a crushed mass of bone, with the isolated left squamosal rotated and exposed anterodorsal to the well-preserved and well-delineated left quadrate. The latter shows a broad expansion of the cephalic condyle atop a relatively slender shaft. The quadrate is only weakly concave posteriorly. Little morphological detail is again discernible on the mandible. As in other specimens of Dinocephalosaurus orientalis, the dentary is somewhat expanded anteriorly as it participates in the formation of a reinforced mandibular symphysis. There is no indication of a coronoid process. The way the specimen is preserved suggests the presence of a large, posteroventrally deflected retroarticular process, but since such is absent in other specimens of Dinocephalosaurus orientalis, this appearance must be due to breakage and deformation, and a dislocation of the left mandible and left quadrate relative to one another.

Three teeth are preserved in situ on the left premaxilla, of which the anterior two form premaxillary fangs. A total of 15 teeth are preserved in situ on the left maxilla, of which the anterior four are distinctly larger than the succeeding maxillary teeth. The largest maxillary fang is the fourth tooth preserved in the tooth row, behind which the maxillary teeth gradually decrease in size. A total of at least 12 dentary teeth can be counted as preserved in situ, of which three enlarged anterior fangs are located in between the posteriormost preserved premaxillary tooth and the anteriormost preserved maxillary tooth. This again suggests a diastema in the upper tooth row in the area of the relatively slender anterior process of the maxilla that lines the lateral margin of the anterior end of the antorbital recess housing the external naris. It appears possible, however, that a much smaller maxillary tooth located in front of the anterior maxillary fangs is largely concealed by the third dentary fang. The large anterior fang-like teeth are only weakly recurved if at all, and the more posterior teeth are upright. All teeth are pointed, the enamel surface striated apically. Especially in the larger teeth, plicidentine infolding is apparent at the base of the tooth.

2.6.2. The vertebral column

(Table 1). The atlas and axis are not exposed in ZMNH M8752. The elongated and slender third cervical vertebra protrudes from below the left mandible. Starting with cervical vertebra 3, the cervical vertebral column is well preserved and exposed in left lateral view in an articulated series up to cervical vertebra 28 (Fig. 9). The general morphology of the cervical vertebrae is again very similar to that observed in other specimens of Dinocephalosaurus orientalis. The cervical vertebrae 23 through to 25 are broken and incompletely preserved, but the neck vertebrae in front of that break are longer and more delicately built than vertebrae 26 to 28. The first 20 cervical vertebrae are elongated and slender, with a very shallow neural crest that retains a concave dorsal margin in lateral view. This results in antero- and posterodorsal neural crest projections located in between the pre- and postzygapophyses respectively. The epipophyses dorsal to the postzygapophyses form a distinct, slender, posterior projection capping the more sturdily built prezygapophyses as they extend well beyond the posterior margin of the centrum. The articular facets for the cervical ribs are located low on the centrum near its anterior margin. The intervertebral articulation between the centra is somewhat obliquely oriented, slanted in an anterodorsal–posteroventral direction. The 26th through to the 28th cervical vertebrae increase in depth but decrease in length. The centrum gains in height, as does the neural crest, which develops a convex dorsal margin. In cervical 27, and even more so in cervical 28, the neural crest furthermore develops into an increasingly distinct posterior projection located in between the postzygapophyses. Up to the tenth cervical, the cervical ribs are deflected away from the posteriorly bent neck. They show the typical structure with a medially directed articular head that is oriented at right angles to the much-elongated shaft, and that carries a free-ending anterior process. Starting with cervical 11, the cervical ribs retain their natural position, together forming a tight bundle of bony rods that runs along the ventrolateral aspect of the cervical vertebral column, obscuring the ventral margin of the centra.

At the position of cervical 28, the cervical series partially disappears below four segments of the proximal caudal vertebral column that have snapped and separated but still remain clustered. At the transition from neck to trunk, the vertebral column turns around and becomes fully exposed again from below more distal parts of the tail (Fig. 9). The anterior region of the dorsal vertebral column is intersected by the neck (cervical 23 to 25). Subsequent, more posteriorly located dorsal vertebrae have been subjected to crushing, distortion or incomplete preservation. A complete count of 62 presacral vertebrae (including the non-exposed atlas and axis) is nonetheless possible, comprising 32 cervical vertebrae and 30 dorsal vertebrae.

Behind the elements of the pectoral girdle five dorsal vertebrae are located, which are well preserved and exposed (Fig. 9). They show the marked lateral as well as ventral constriction of the centrum, and the sturdily built neural arch that forms the tall, anteriorly deeply excavated transverse processes. The pre- and postzygapophyses are symmetrically developed, the plane of articulation between them horizontally oriented. The neural spine is distinct, marked by essentially rectangular contours but slanting slightly backwards. Progressing backward within the dorsal region, the neural spines become more prominent, increasing both their height as well as their antero-posterior dimension. The anterior dorsal ribs form evenly curved elements; more posterior dorsal ribs are mttore pronouncedly curved in the proximal ‘shoulder’ region. The dorsal ribs are distally slightly expanded and form a distinct articular head proximally.

As is true of the posterior dorsal vertebrae, the sacrum is poorly preserved (Fig. 9). It is possible to identify two sacral vertebrae, which however offer no relevant anatomical detail.

The tail in ZMNH M8752 is broken into several segments in its proximal part. A total of 69 caudal vertebrae are preserved (Fig. 9 ) but this is an incomplete count. The first few caudal vertebrae are partially obscured by overlying elements of the left hindlimb (femur and tibia). Caudal ribs are associated (not fused) with the first six caudal vertebrae. They decrease in both width and length in a posterior direction. Small, ‘stubby’ transverse processes can be identified on three more caudal vertebrae, but there is no evidence of caudal ribs being present beyond the ninth caudal. The neural spine morphology again shows significant changes within the caudal vertebral column (Fig. 10). Of essentially rectangular shape in the first six caudal vertebrae, they resemble those of the posterior dorsal vertebrae. Between the sixth and the ninth caudal vertebra, the neural spines begin to assume rounded contours (i.e., with a distinctly convex dorsal margin in lateral view), which become fully expressed beyond the ninth caudal vertebra resulting in a highly distinctive morphology. Very prominent anteriorly, the neural spines gradually decrease in size posteriorly, particularly past the 39th caudal vertebra. More posteriorly, beginning around the 40th to 43rd preserved caudal vertebrae, the neural spines start to form a posterodorsally directed projection. Prominent at first, and characterised by an anteroposterior expansion towards the distal end, the neural spines progressively decrease in size more posteriorly; the last, diminutive rudiment of a neural spine can be identified on the 65th preserved caudal vertebra. The chevrons similarly show a changing morphology along the caudal vertebral column (Fig. 10). Articulating in an intervertebral position, they form a broad plate-like ventral expansion of rounded contours in the anterior tail region, mirroring the neural spines in their structure (Fig. 10a). Again, in the area of the 40th through to the 43rd preserved caudal vertebrae, the chevrons are seen to gradually change their shape, forming an inverted T-bar, the stem of which articulates in an intervertebral position on the ventral edge of the centra (Fig. 10b, c). This morphology is not unique to Dinocephalosaurus orientalis, as a somewhat similar distal expansion of the chevrons is also present in Trilophosaurus buettneri (Spielmann et al. Reference Spielmann, Lucas, Rinehart and Heckert2008). Again, the chevrons continue to gradually decrease in size in a posterior direction; the last diminutive chevron articulates on the 64th and 65th preserved caudal vertebrae respectively.

Figure 10 Dinocephalosaurus orientalis, ZMNH M8752, detailed drawings of selected caudal vertebrae. (a) Anterior caudal vertebraea in right lateral view. (b) Mid- to posterior caudal vertebrae in right lateral view. (c) Posterior caudal vertebrae in right lateral view. Abbreviations: ca.c = caudal centrum; chv = chevron; ns = neural spine.

The gastral rib basket is preserved in a somewhat disarticulated condition in the anterior, middle and posterior trunk region (Fig. 9). Particularly in the anterior trunk, it can be ascertained that each gastral rib is composed of three elements: an angulated midventral element, the apex pointing anteriorly, and two collateral elements that meet the midventral element in an overlapping contact, and that are slightly curved in their lateral part.

2.6.3. The pectoral girdle and forelimb

The distal (dorsal) ends of both left and right clavicles are exposed, their proximal ends being buried below the caudal vertebral column. The distal part of the clavicle is evenly curved and tapers to a blunt tip. The left scapula is preserved in articulation with the left coracoid, which itself is incomplete. The scapular blade forms a kidney-shaped ossification with a convex dorsal and concave ventral margin that carries a glenoid process near its posteroventral end. The length of the scapula is 80 mm and its depth is 51.1 mm. The left coracoid is less well preserved, but shows the coracoid foramen to be located in its anterior part, in front of and below the glenoid facet. The right scapulocoracoid is not preserved or exposed.

Both forelimbs are preserved in ZMNH M8752, but the left one is better exposed than the right one (Table 3), which is partly obscured by rib fragments (Fig. 9). The humerus in ZMNH M8752 is rather straight, as is also the case in ZMNH M8728, whereas it appears curved in ZMNH M8727, which is probably attributable to its angle of preservation. The proximal head of the left humerus is incomplete; its minimal width at mid-shaft is 17 mm and its distal width is 30 mm. The length of the right humerus is 103 mm, but both its proximal and distal ends are not fully exposed, such that their width cannot be measured. An entepicondylar foramen is absent. The ectepicondylar groove, as well as the distal ectepicondylar notch, are weakly expressed. The left radius and ulna are very well preserved and exposed. Again, as in ZMNH M8728, the radius is somewhat more robustly built than the ulna. The radius shows marked expansions both proximally and distally, which result in a biconcave shaft, the postaxial margin of which is more deeply concave than the preaxial margin. The ulna is distinctly expanded proximally, but only weakly expanded distally. Its preaxial margin is concave, although less so than the postaxial margin of the radius. Together, the two elements define the spatium interosseum. The postaxial margin of the ulna is rather straight, yet damaged in its distal part.

Six carpal elements are ossified and preserved in the left manus. The proximal row of carpal elements of pentagonal circumference is preserved in articulation. Of those, the intermedium is the largest (maximum exposed length: 15.4 mm), followed by the radiale (15.2 mm) and the ulnare (14.3 mm). The distal carpal row comprises three ossifications of rounded contours, a large distal carpal 4 and smaller distal carpals 3 and 2. The metacarpals of the left manus are deflected away from the distal carpal ossifications and have been pushed up against one another, partially obscuring metacarpal V. Metacarpals I through to IV are all straight elements, with expanded proximal and distal ends and a biconcave shaft. Metacarpal V, well exposed in the right manus, is short and somewhat more massively built. Of all metacarpals, mcIII is the longest in the left manus, mcIV is the longest in the right manus and mcV is the shortest in both (Table 3).

Preservation of the phalanges is incomplete in the left manus. Digit II preserves two phalanges, digit III comprises two phalanges (a third one possibly lying atop a dorsal rib) and digit IV preserves three phalanges – evidently an incomplete count.

In the right forelimb, radius and ulna are partially obscured and crossing over each other. In the proximal carpal row, the radiale, intermedium and ulnare are identifiable yet less well preserved and exposed than in the left manus. The distal carpal ossifications cannot be located except for one that protrudes from below a phalanx. A total of nine disarticulated phalanges can be identified.

2.6.4. The pelvic girdle and hindlimb

As mentioned above, the sacral region is poorly preserved in ZMNH M8752, although two sacral vertebrae are identifiable. Neither ilium can be identified, but the ventral part of the left pubo-ischiadic plate is well preserved and exposed. It shows that, at least in their ventral parts, both the pubis and ischium are broad, plate-like ossifications, which meet each other for most of their depth in a suture. The thyroid fenestra is thus eliminated. The fact that this is not a primitive condition but a secondary development is indicated by the persistence of a small yet distinct cleft between pubis and ischium in the ventral margin of the pubo-ischiadic plate.

Both hindlimbs are preserved, but the left one is broken across the clustered segments of the proximal caudal vertebral column (Fig. 9). The femur is a rather straight element that is both proximally and distally expanded. Its preaxial (anterior) margin is at best only slightly concave, while the postaxial (posterior) margin is more distinctly concave. Like the other zeugopodial and stylopodial elements, the femur shows little morphological differentiation. The internal trochanter is not distinct and the articulation for tibia and fibula is continuous. The proximal end of the right femur is crushed and distorted.

The tibia and fibula are well preserved and exposed in the left hindlimb. The tibia is broadly expanded proximally, but less distinctly expanded distally. The shaft is biconcave, with the postaxial margin more deeply excavated than the preaxial margin. The proximal end of the tibia has straight pre- and postaxial margins, and its proximal margin is incomplete (broken). The fibula is only weakly expanded proximally, but it is very broadly expanded distally. Its preaxial margin is deeply concave, its postaxial margin slightly convex. Together, the tibia and fibula define the spatium interosseum distal to which the astragalus is located.

The left tarsus comprises three ossifications of rounded contours. The astragalus, located distal to the spatium interosseum in an intermedium position, is the largest (maximum exposed length: 18.5 mm), followed by the calcaneum (17.5 mm) located distal to the fibula; the distal tarsal IV (11.6 mm) is located proximal to metatarsal IV (Table 5). All five metatarsals are beautifully preserved and exposed in the left foot. The first metatarsal is distinctly shorter than the other ones and almost of rectangular contours. All other metatarsals are straight elements with somewhat expanded proximal and distal ends and a biconcave shaft; there is no overlap of their proximal heads. Of all the metatarsals, mtIII is the longest. Other than the most proximal ones, the phalanges of the left foot are obscured by overlying caudal vertebrae. The right foot, broken across a proximal segment of the tail, allows a phalangeal count in the fourth digit only, which shows five phalanges (four phalanges and an ungual) – the primitive number.

2.7.1. The skull and mandible

(Figure 12). The skull is 201 mm long and 108.7 mm wide across the temporal region as preserved. At the anteriormost end, the premaxillae have separated slightly along the midline. This is the result of dorsoventral compression of the skull, causing the anterior end to be somewhat splayed laterally. Clearly defined medial processes of the premaxillae extend posteriorly together over one third of the total length of the skull. The sutures marking the edges of the maxillae are clearly marked on both sides and are mirror images of each other. The sutures separating the nasals from the frontals and the parietal from the frontals are less clearly distinguishable, but they generally seem to follow the pattern in the holotype with interdigitating sutures. The presence of the distinctive narial gutters (antorbital recess) extending posteriorly from the external nares likewise mirrors the morphology of the holotype. The frontals are broad anteriorly where they meet the prefrontals, but they become noticeably constricted posteriorly, where they form the posterodorsal borders of the orbits. The frontals of most non-archosauriform archosauromorphs are also somewhat constricted in the interorbital region, with the notable exceptions of Tanystropheus hydroides and Tanystropheus longobardicus, in which the frontals are widened above the orbits, covering them dorsally (Nosotti Reference Nosotti2007; Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020a, Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020b). There is a pronounced interdigitating median suture separating the frontals just anterior to the parietal. The parietal table is narrow, but flares posteriorly into the parietal ‘wings’ marking the posterior borders of the sub-circular supratemporal fenestrae. These parietal ‘wings’ are oriented posterolaterally as in most early archosauromorphs, except Tanystropheus spp., Protorosaurus speneri and Azendohsaurus madagaskarensis, which exhibit a lateral orientation of these processes (Gottmann-Quesada & Sander Reference Gottmann-Quesada and Sander2009; Flynn et al. Reference Flynn, Nesbitt, Michael Parrish, Ranivoharimanana and Wyss2010; Spiekman et al. Reference Spiekman, Neenan, Fraser, Fernandez, Rieppel, Nosotti and Scheyer2020a). The prominent pineal foramen is of an elongate oval shape. A pineal foramen is generally present in most non-archosauriform archosauromorphs, although it is missing in Macrocnemus spp., Trilophosaurus buettneri, certain specimens of Prolacerta broomi and the putative archosauromorph Czatkowiella harae (Spielmann et al. Reference Spielmann, Lucas, Rinehart and Heckert2008; Borsuk-Białynicka & Evans Reference Borsuk-Białynicka and Evans2009; Spiekman Reference Spiekman2018; Miedema et al. Reference Miedema, Spiekman, Fernandez, Reumer and Scheyer2020). The postfrontal is an elongated bone, oriented transversely relative to the longitudinal axis of the skull. On its medial end it articulates with the parietal on its posterior half and the frontal on its anterior half. This configuration corresponds with that of the holotype as outlined above (following the interpretation of Rieppel et al. Reference Rieppel, Li and Fraser2008). As with the holotype skull, the strong dorsoventral crushing of the skull hampers observation of the relationship between the squamosal, postorbital and jugal. The postorbital in particular is badly broken and incomplete, and the dorsal portion of the jugal is also poorly preserved.

Figure 12 Dinocephalosaurus orientalis IVPP V20295. Detail of skull in dorsal view. (a) Photograph. (b) Photograph with interpretative drawing. Abbreviations: fr = frontal; la = lacrimal; mx = maxilla; n = nasal; pa = parietal; pl = palatine; pm = premaxilla; po = postorbital; prf = prefrontal; pt = pterygoid: rap retroarticular process.

Parts of the palate can be observed in dorsal view through the orbit and supratemporal fenestra. On the right side a clear articulation is observed between the broad pterygoid and palatine, whereas the exact articulation between these elements is unclear on the left side. An additional disarticulated element is poorly preserved, but based on its relative position it might represent an ectopterygoid. Posteriorly, the articulation between the quadrate ramus of the pterygoid and the pterygoid wing of the quadrate is well preserved, with the latter overlapping the former laterally.

The two large ‘fangs’ seen on the maxilla of the holotype are not readily apparent in this new specimen, although the base of one such tooth has been exposed on the right side with the distal part extending into the matrix. The larger teeth develop striations towards the apex of the enamel crown, as in the other specimens. On the left side a break in the block has resulted in the loss of the posterior end of the premaxilla and the anterior portion of the maxilla. Nevertheless, each premaxilla is seen to bear at least one large tooth, and on the right side two similar teeth project up from the mandible. On the right side, two mandibular teeth can be observed through the orbit as a result of the deformation of the specimen. Two very weakly developed retroarticular processes can be seen behind the temporal region on both sides.

2.7.2. The vertebral column

(Table 4). The neural arch elements of the atlas are slightly displaced, but essentially the neck is in complete articulation with the skull. The first 22 cervical vertebrae flex around to form an almost complete circle with the tip of the snout before the series continues, passing backwards under the posterior region of the trunk immediately in front of the pelvis and straight back to the pectoral girdle. The cervical ribs of the first 17 cervical vertebrae have moved out of natural articulation with the individual vertebrae, lying in bundles just to one side of the neck. However, from cervical 18 onwards they are more closely articulated with their respective vertebrae.

Table 4 Length and height of the sacral and caudal vertebrae, specimen IVPP V20295. Abbreviations: CAV = caudal vertebra; SV = sacral vertebra. The length was measured across the ventral margin of the centrum; the height was measured across mid-centrum and includes the neural crest. All measurements are in mm.

In ZMNH M8728 (above) we noted a change in the form of the cervical vertebrae from a less concave ventral margin in lateral view together with an increase in the height of the neural spine at cervical 24. They also become shorter at this point. It would seem that this change in morphology might take place at vertebra 22 in IVPP V20295, although it should be noted that this is also exactly the region where the neck is overlain by the curled dorsal vertebrae and it is therefore somewhat difficult to assess this with complete confidence. Where the neck emerges from under the dorsal vertebrae, the vertebra (considered to be cervical vertebra 25) is very poorly preserved.

Cervical vertebra 27 has a neural spine that is much anteroposteriorly narrower and slightly taller than the preceding cervical vertebrae. The posteriormost cervical vertebrae (presacral vertebrae 28–32) together with the anterior dorsal vertebrae have characteristic neural spines that take the form of a relatively narrow backward-pointing hook. The transition to the dorsal vertebrae seems to be partially marked by this neural spine having a slight anterior projection or knob (forming a weak T-shape in lateral view). Whereas all the preceding cervical ribs have a clear anterior process and a posteriorly curving shaft, the rib of presacral vertebra 32 is transitional; it lacks an anterior process and its shaft is straight but posteroventrally directed, relatively short, and with a blunt distal end. Since this rib is considerably shorter than the subsequent dorsal ribs and does not seem to contribute to the dorsal rib cage, its corresponding vertebra is identified as the posteriormost cervical, as in ZMNH M8728.

In contrast to Tanystropheus hydroides, the neck of Dinocephalosaurus orientalis is often preserved strongly flexed, and in IVPP V20295 the neck is coiled to the extreme. As in other specimens, many of the ribs have ‘popped out’ of position – not flexed nor broken, so that they retain their long straight shafts. This may simply be because of the relatively shorter but greater numbers of vertebrae allowing the neck to flex postmortem. It is very unlikely that the neck was so flexible in life. The ribs certainly maintain a straight position with no major flexion. Although the rib heads may have been displaced away from the vertebral column, they still remain very much aligned with their respective vertebrae – they have moved relatively little forward or backward from the positions in life. This is perhaps indicative of these splayed ribs being encased by skin at the time of burial. On the other hand, although shorter than in Tanystropheus in absolute terms, they do traverse a greater number of intervertebral joints – five is a typical number crossed – which in the absence of any dewlap would suggest a degree of rigidity from these bundles of ribs.

The first six dorsal vertebrae are slightly out of articulation with each other and describe a tight radius. There is then a small break followed by the remaining dorsal vertebrae that complete the circular disposition of the body. There are either 29 or 30 dorsal vertebrae depending on which vertebra is considered the first sacral, but 30 is considered the most likely.

Where the posteriormost cervical and anteriormost dorsal vertebrae lie alongside the proximal tail, the vertebrae are rather poorly preserved and the bone surface is very fragmented. The same condition also pertains to most of dorsal vertebrae 5–15, as well as sections of the caudal vertebrae including those situated alongside the first two dorsal vertebrae.

The neural spines of all the dorsal vertebrae are relatively small and narrow, but expand distally into a low, rugose ridge, so that they are broadly T-shaped in lateral view. As in all other specimens, the anterior dorsal vertebrae (1 through to approximately 12) have very distinctive and well developed transverse processes with a deeply excavated anterior surface and a concomitantly markedly convex posterior edge. They are also very tall and narrow. In the region of dorsal vertebra 13 or 14 the height of the transverse process is somewhat reduced and the diapophysis becomes more prominent and circular. This reduction in height and development of a more circular facet for the rib continues to the sacral vertebrae.

For the most part the dorsal ribs lie disarticulated from the vertebrae, but still in close association. They are all single-headed, but anteriorly they have deeper heads with what could be described as a more robust tuberculum portion that extends ventrally into a narrow and elongate capitulum region. In the more posterior ribs, the heads become more rounded, corresponding to the reduction in complexity of the transverse processes.

The short transverse processes on vertebrae 60–63 are quite pronounced, with those on 61 and 62 being the largest, and which we regard here as the two sacral vertebrae. Yet at first glance vertebrae 61 and 62 also seem to have associated ‘haemal spines’, which is hard to reconcile. However, on closer inspection, it is clear that these ‘haemal spines’ have exceptionally anteroposteriorly flared distal rami and it is almost certain that they represent sacral ribs that have been displaced, in turn indicating that they were not fused to the sacral vertebrae. These ribs are also consistent with the element thought to be a sacral rib overlying the top edge of the left ilium. If they are sacral ribs then there are only four preserved, which in turn is indicative of just two sacral vertebrae, the number present in all known non-archosauriform archosauromorphs. Equally, it does not appear as though both ribs could articulate with the ilium, as the iliac blade is so reduced (see below). Vertebra 63 also has a broad and prominent facet on the end of a short transverse process, but it must be assumed to be the first caudal. It would have been impossible for the associated rib to have made any contact with the pelvis.

The left femur partially covers the neural spines of the last dorsal, both sacral and the anteriormost caudal vertebrae. In addition, the left fibula partially obscures the second caudal, so it is not possible to state unequivocally whether there is a distinct change in the nature of the neural spines between the dorsal vertebrae, sacral vertebrae and caudal vertebrae. However, from what is exposed of these elements, it would appear that both sacral vertebrae have relatively tall neural spines that are rectangular in lateral view, a condition shared with the anterior caudal vertebrae. This contrasts with the somewhat ‘waisted’ (or weakly T-shaped) appearance of the preceding dorsal neural spines terminating in a distinctly rugose surface.

It is difficult to measure the dimensions of the dorsal vertebrae (Table 4) because of the way the torso curls around on itself and the ribs overlap the vertebrae, but dorsal vertebrae 6 and 7 (although distorted) are clearly exposed and provide potentially useful reference points for other specimens, as does dorsal vertebra 20.

The tail is preserved completely intact and fully articulated with a complement of 81 vertebrae. The mid to distal tail is beautifully exposed, and displays the remarkable hatchet-shaped chevrons mirroring the rounded neural processes. The first haemal arches are quite broad-based and occur in the first two caudal vertebrae. At least the first ten – if not more – caudal vertebrae have a ‘typical’ rectangular neural spine and chevron bones. The transition to the hatchet-shaped form appears to begin at around caudal 16, although bones of the pectoral girdle obscure part of the tail in this region. The chevrons become much shallower and more elongate at caudal 44, and there is also a change in shape, so that the ventral edge is convex in lateral view. At about the same point there is also a noticeable shift in the shape of the neural spines so that they are more inclined posteriorly and more clearly expressed on the posterior half of the vertebra. The chevrons and neural spines progressively diminish in size but the chevrons can still be clearly distinguished as separate elements even as far posteriorly as caudal 75, where the centra is a mere disc of bone.

The gastralia are loosely associated and extend from about the sixth dorsal vertebra back as far as the sacrum. As in other specimens, they display two different morphologies: the medioventral elements that are slightly angulated and the collateral elements that terminate in a blunt tip proximally and a slender tapering tip distally.

2.7.3. The pectoral girdle and forelimb

Both pectoral girdles and forelimbs are almost intact and only partially disarticulated. The left limb and girdle lie a short distance from the vertebral column and are missing the proximal head of the humerus and the glenoid portion of the coracoid. The right pectoral girdle is also displaced from its natural position and lies partially under the dorsal ribs (the scapula) and over the proximal tail (the coracoid) where it coils around the body. Both the scapula and coracoid are kidney-shaped elements of approximately equal size, the scapula just marginally larger in the development of the posterodorsally projecting scapular blade. The posterior margin of the coracoid is deeply notched below the level of the glenoid fossa, and there is a distinct coracoid foramen. Neither interclavicle nor clavicles are preserved.

The humeri and epipodials are all columnar elements with minimal development of the proximal and distal heads. The left radius almost completely overlies the left ulna, and in the right limb the radius is also out of position. The arrangement of carpals is difficult to discern as both wrists overlap. Nevertheless, there is a total of 12 circular carpals and therefore presumably a total of six in each wrist. As preserved in the left forelimb the phalangeal formula is 1:2:3:5:1 (Table 3), but the terminally preserved hourglass-shaped phalanges are similar in form to all the other phalanges and are not spatulate or claw-shaped as might be expected for unguals. The right forelimb is a bit disrupted where it extends over the left forelimb, and digits 1 and 2 are disassociated. However, digit 3 bears three phalanges, digit 4 has six phalanges, with the terminal one being expressed as a small round disc, and in digit 5 just a single phalanx is preserved. Thus, it would seem that terminal phalanges fail to ossify in this taxon.

2.7.4. The pectoral girdle and hindlimb

(Figure 13) Of all the specimens of Dinocephalosaurus orientalis described here, the elements of the pelvis are the most clearly displayed in IVPP V20295. There is no definitive embayment constituting the thyroid fenestra between the pubis and ischium, although there was almost certainly a deep notch along the articulation between the two towards the median symphysis.

Figure 13 Dinocephalosaurus orientalis IVPP V20295. Detail of left hindlimb as preserved. Abbreviations: ac = acetabulum; as = astragalus; ca = calcaneum; ect = ectopterygoid; in tr = internal trochanter; mt = metatarsal; po p = posterior process of the ilium; pu f = pubic foramen: sa.r = sacral rib.

The three elements of the left pelvic girdle have separated slightly from each other, with the ischium and ilium almost in their original position relative to each other. The pubis has been pushed forward slightly by the intervention of the right femur and ischium. The pubis is an almost circular element that is slightly larger than the ischium. It bears a rugose area on its dorsal margin that articulated directly with the ilium. The ischium is of an approximate trapezoidal shape with the posterior margin being slightly convex, resulting in a very weak posterior process. The left ilium is complete but the small dorsal process is partially covered by the second sacral rib. This dorsal process is not developed anteriorly at all (i.e., a preacetabular process is completely absent) but has a short, poorly developed posterior projection (i.e., a postacetabular process). The acetabulum is shallow and the acetabular contribution of the ilium is semi-lunate shaped.

The right ilium is not obviously visible, but it is probably covered by the left pubis. A short section of bone extending between the left pubis and left ilium apparently represents a short section of the dorsal process of the right ilium. The right pubis lies just anterior to its left counterpart. It displays a weakly developed bony strut extending anteroventrally from the margin of the acetabulum. The right ischium is draped over and closely oppressed to the proximal half of the femur, such that the boundaries of the femur can be clearly distinguished through the plate-like ischium. The anterior margin is a little fragmented and the posterior margin is covered by the left ischium so that it adds nothing further to the description.

The right hindlimb is almost in full articulation so that the proximal head of the femur appears to be resting within the acetabulum, although it is covered by the ischium. The left femur preserves a clear internal trochanter, which is proximodistally straight. Proximally, the trochanter does not quite reach the proximal end of the femur. The femur is a robust, relatively straight element, and the tibia is the more robust of the two columnar epipodials, which bow away from each other to leave a prominent spatium interosseum as in all other specimens. The only tarsal elements preserved are the astragalus and calcaneum, and these are simple rounded discs that are not in contact with each other. There is a noticeable gap between the proximal carpals and the metatarsals, strongly implying that distal carpals were not ossified.

Unfortunately, the distal end of digit 3 is missing on the block, but the other four digits would appear to be complete. If so, this gives the rather unusual formula of 1:2:?:2:1 with the third digit having a minimum of three phalanges (Table 5). The left hindlimb is more disarticulated with the femur and epipodials draped over the proximal tail, although the fibula is deflected away from the tibia distally. The astragalus and calcaneum lie on top of the neural spines of the sixth and seventh caudal vertebrae, and the digits extend backward below the tail. However, only three digits are clearly exposed. The longest digit (likely digit 3) has six phalanges including a blunt spatulate-shaped terminal phalanx.

Table 5 Length and width of hindlimb elements in the two specimens preserving the hindlimbs, ZMNH M8752 and IVPP V20295. Abbreviations: L = length; PW = proximal width; MW = minimal width; DW = distal width. All measurements are in mm.

2.7.5. Remains in the abdomen

(Figure 14). Within the body cavity in the mid-dorsal region lie the remains of a minimum of four fishes. Their scales clearly overlap the right ribs, but are under the left ribs. At least one of these fishes, the most complete, can be referred to the genus Lashanichthys, a holostean. In addition, two partially preserved specimens lying close by, probably belong to the same taxon. A larger specimen with distinct ganoid scales is possibly a member of the genus Colobodus, which is known from Panxian (currently known as Panzhou) (e.g., Sun et al. Reference Sun, Tintori, Lombardo, Jiang, Hao, Sun, Wu and Rusconi2008). Further posteriorly, there are remains of a number of small vertebral elements and a possible limb bone. These could conceivably represent an embryo, or alternatively are the remnants of a small prey reptile, but their identities remain equivocal. The three most complete of the tiny vertebrae lie on top of the 23rd cervical. One has a distinct and quite broad neural spine that is perhaps not entirely consistent with any of the Dinocephalosaurus vertebrae apart from the axis. The limb element is a straight shaft with no distinct enlargement of either end and is 26.6 mm long.

Figure 14 Dinocephalosaurus orientalis IVPP V20295. Detail of gut contents (fishes) in gastral region. On the left is a complete specimen of Lashanichthys sp. and on the right a partial specimen referred to Colobodus sp.