Bulbasaurus SAM-PK-K10587.png

''Bulbasaurus'' (meaning "bulbous reptile") is an extinct genus of dicynodont that is known from the Lopingian epoch of the Late Permian period of what is now South Africa, containing the type and only species ''B. phylloxyron''. It was formerly considered as belonging to ''Tropidostoma''; however, due to numerous differences from ''Tropidostoma'' in terms of skull morphology and size, it has been reclassified the earliest known member of the family Geikiidae, and the only member of the group known from the ''Tropidostoma'' Assemblage Zone. Within the Geikiidae, it has been placed close to ''Aulacocephalodon'', although a more basal position is not implausible.

''Bulbasaurus'' was ostensibly not directly named after the Pokémon Bulbasaur, but rather after its nasal bosses, which are unusually bulbous among geikiids; however, the describers noted that the similarity in name "may not be entirely coincidental." Additionally, the specific name of the type species means "leaf razor", which is most directly a reference to its keratin-covered jaws. Other distinguishing characteristics of ''Bulbasaurus'' among the geikiids include the hook-like beak, very large tusks, and absence of bossing on the prefrontal bone.

Discovery and naming

The holotype specimen of ''Bulbasaurus'' was found by Roger M.H. Smith in the Vredelus locality, which is located at an altitude of , in the district of Fraserburg, Northern Cape, South Africa. This locality is part of what is known as the ''Tropidostoma'' Assemblage Zone, which belongs to the Lopingian (upper Permian) Hoedemaker Member of the Middle Teekloof Formation. The ''Tropidostoma'' AZ is named after the oudenodontid ''Tropidostoma'', which occurs commonly at the site. The holotype itself, which is catalogued as SAM-PK-K11235, is a partially complete skull that is missing the left subtemporal and both postorbital bars. It was discovered lying right-side-up in a bed of grey siltstone with embedded micrite nodules, and there were no associated remains from the rest of the skeleton. "Head-only" preservation is common in therapsid fossils of the Hoedemaker Member, because the specimens were probably left out in the open and became disarticulated before being rapidly buried by flash floods.

Other referred specimens include the nearly-complete skull CGP/1/938 (from the Wilgerbosch Kloof locality in Fraserburg), the complete skull CGP/1/949 (also from Wilgerbosch Kloof), the complete skull with associated lower jaws and postcranial remains CGP/1/970 (from the Blaauwkrans locality in Beaufort West, Western Cape), the complete but crushed skull CGP/1/2263 (locality unknown), the crushed skull with lower jaws SAM-PK-K10106 (from the Paalhuisberg locality in Beaufort West), and the complete juvenile skull with lower laws SAM-PK-K10587 (from the Doornhoek locality in Beaufort West). All of these specimens are either held at the Iziko Museums in Cape Town or the Council for Geoscience in Praetoria. Before being referred to the new genus ''Bulbasaurus'', they were initially treated as specimens of ''Tropidostoma'' in collections.

''Bulbasaurus'' was described by Christian Kammerer and Smith in 2017. The description states that the generic name combines the Latin ''bulbus'', referring to the very large and bulbous nasal bosses, with the common suffix ''-saurus''. As for the specific name ''phylloxyron'', meaning literally "leaf razor", it is derived from the Greek and , and apparently refers to the keratinous covering on the premaxilla, maxilla, and palate that would have been used to shear plant material. Thus, as published, the name of ''Bulbasaurus'' does not directly refer to Pokémon, or specifically the similarly-named Bulbasaur. However, Kammerer noted that "if one wished to read between the lines concerning certain similarities, I wouldn't stop them", and later added that "similarities between this species and certain other squat, tusked quadrupeds may not be entirely coincidental."

Description

Premaxilla, maxilla, and palate

At the front of the upper jaw of ''Bulbasaurus'', the tips of the fused premaxillae are strongly hook-like, much more so than ''Tropidostoma'' and other dicynodonts but not as much as ''Dinanomodon''. Also unlike ''Tropidostoma'', the flattened front face of the premaxillae bear a tall, narrow, prominent ridge; '' Aulacephalodon'' also has a similar ridge, albeit broader and not as sharp. The back of the premaxillae narrow and extend between the roughened bosses on the nasal bones. Viewed from underneath, the bone is roughly pentagonal; the bottom surface bears two ridges near the front, as well as an additional ridge extending backward from where the two forward ridges end, which gradually becomes taller and wider. These ridges are separated by depressions in the bone of roughly equal depth, which is like other geikiids but unlike ''Tropidostoma''. At the outer extremities of the premaxillae, low and roughened ridges are located near the base of the tusks.

Further back on the interior of the upper jaw, the palatine bones are exposed as a palatine pad, which is very roughened and would have been covered in keratin, although the portion where they contact the premaxillae is smooth and sloping. The back portion of the palatines are thinner than the rest of the bone, but it is still thicker than that of either ''Tropidostoma'' or ''Oudenodon'', instead resembling ''Aulacephalodon'' more closely. The pterygoid bones are robust in contrast to ''Tropidostoma'', and bear ridges that converge into a tall, blade-like process known as the . The pterygoids also project outwards in rod-like structures to meet the quadrate bones.

Compared to other dicynodonts, the maxillary tusk of ''Bulbasaurus'' was massive; the holotype skull, which is long, has a tusk diameter. Only ''Aulacephalodon'' has comparably large tusks proportionally, but these belong to adult specimens much larger than ''Bulbasaurus'' (in juveniles the size of ''Bulbasaurus'', the tusks are still erupting). The root of the tusk bulges outwards from the surface of the maxilla due to its large size. Extensive pitting on the surface of the maxilla is suggestive of some kind of keratinous covering, which has also been inferred for other dicynodonts. Unlike other geikiids and most other cryptodontian dicynodonts, there is no ridge behind the tusk, although mature ''Aulacephalodon'' also lack this ridge.

Nasal and orbital rim

The nasal bones, which form the roof the snout, bear a pair of enlarged bosses of bone as in other cryptodontians. In contrast to the small, oval-shaped, relatively narrow, and smooth-textured bosses of ''Tropidostoma'', the roughened bosses of ''Bulbasaurus'' are very large and nearly form a single continuous boss (although a narrow strip of the premaxilla extends backwards between the bosses). ''Aulacephalodon'' and '' Pelanomodon'' also have large and roughened bosses, but they are separated in part by the nasals. At the back of the bosses, a slight indentation wrapping around the top and sides of the skull separates them from the eye socket, typical of cryptodontians except for '' Odontocyclops''. The suture between the nasals and the frontal bones is slightly raised relative to the rest of the skull; the same raised suture is also seen in ''Aulacephalodon'' and ''Pelanomodon''.

Typical of geikiids, the interorbital region between the eyes was quite broad. The lacrimal bones, prefrontal bones, frontal bones, and jugal bones form the margin of the eye socket, with the portion comprised by the lacrimals having an orbital ridge that is better-developed and more raised. Unlike other cryptodontians, there is no evidence of a second set of bosses on the prefrontals, although their surfaces are somewhat thickened. A relatively deep midline depression (mildly developed in ''Tropidostoma'' and ''Oudenodon'', but absent in other geikiids) is visible on the frontals, which are situated largely between the eyes and form roughened edges where they contributes to the rims of the eye sockets. There appears to be no separation of the postfrontal bones from the frontals, which is probably an adult characteristic as in ''Aulacephalodon''. The elongate jugals form part of the zygoma, or bony cheek, and ends at the temporal fenestra. It also forms part of the temporal and postorbital bars; ''Pelanomodon'' differs from ''Bulbasaurus'' in having small bosses on the latter portions of the jugals.

Postorbital skull

Most of the postorbital bar is made up of the postorbital bones, which are very robust relative to other cryptodontians as in other geikiids. However, compared to other geikiids, the postorbital bar of ''Bulbasaurus'' is relatively smooth and free of bosses. The sides of the postorbitals, which would have anchored jaw musculature, are very concave. Near the back, the postorbitals curve and converge to form a somewhat pinched intertemporal bar that overlaps the parietal bones to varying extents. The squamosal bones also contribute to the postorbital bar; its back edge along the postorbital bar is somewhat twisted in ''Bulbasaurus'', which is seen in other cryptodontians but is taken to an extreme by ''Aulacephalodon'' and ''Pelanomodon'', where the bone has become entirely twisted such that the interior faces outwards. Projections of the squamosal bones partially surround the posttemporal fenestrae on the rear of the skull, like ''Aulacephalodon'', ''Pelanomodon'', ''Oudenodon'', and ''Tropidostoma''.

As for the underlying parietals themselves, they are slightly concave. In front of the parietals are the small midline preparietal bones, which are relatively broad and have a rounded tip, as in ''Aulacephalodon'' and ''Pelanomodon'' but in contrast to ''Tropidostoma''. The pineal foramen is bordered by the preparietals and parietals, and it is surrounded by a simple ridge instead of being on a raised boss like either the large rhaciocephalids and '' Endothiodon'' or some large specimens belonging to ''Aulacephalodon''. On the braincase, no sutures are visible, suggesting that the bones are very fused. The occipital bones are likewise very fused. The contribution of the supraoccipital bones to the back of the skull is unusually extensive and occupies much of the area not part of the squamosals above the level of the foramen magnum. Also unusual are the smaller elements at the back of the skull, namely the postparietals and tabulars. The postparietals are not part of the continuous flat surface at the back of the skull, instead forming a sharp divot; additionally, a strong midline crest is present on the postparietals and do not extend onto other bones. Meanwhile, the tabulars are wider than they are long.

Mandible and postcrania

The mandible of ''Bulbasaurus'' was largely similar to ''Aulacephalodon''. At the front of the mandible, the two toothless dentary bones fuse at the front to form a continuous beak with a sharp, pointed tip. The somewhat convex front surface of this junction, or the dentary symphysis, is separated from the sides of the dentaries by sharp ridges, a condition also seen in ''Pelanomodon'' and ''Geikia'' but not seen in ''Aulacephalodon''. Overall, the dentary was tall and robust, the symphysis more so than the rest of the bone. Located at the mid-height of the dentaries are the mandibular fenestrae, which are small and oval, and bordered on top by a dentary shelf that expands into a boss. Asides from the skull, the other portions of ''Bulbasaurus'' have not been prepared in depth. The ribs are gently curved and are bicipital in that they have two heads. On the humerus, the deltopectoral crest was robust and strongly separated.

Ontogeny

Most skulls referred to ''Bulbasaurus'' are long, with two skulls (CGP/1/2263 and SAM-PK-K10587) being smaller at and respectively. The larger skulls generally belong to mature specimens. While the CGP/1/2263's size is largely due to compression, SAM-PK-K10587 seems to be a genuinely immature individual. Notably, it differs from other specimens in having a shorter and less hooked snout; relatively smaller but still completely erupted tusks; less developed nasal bosses that are more separated by the premaxilla; a narrower interorbital region between the eyes; a wider intertemporal region at the back of the skull; relatively weak depressions in the interorbital and intertemporal regions; no overlap of the parietals by the postorbitals; and minimal twisting of the squamosal on the postorbital bar.

These differences are most likely due to growth, as similar transformations are also seen in ''Aulacephalodon''. However, the latter (and all other geikiids where the growth sequence is known) differs from ''Bulbasaurus'' in that the degree of overlap of the parietals by the postorbitals does not change; instead, the parietals themselves simply become wider. In this respect, ''Bulbasaurus'' retains the ancestral cryptodontian condition, which is also seen in rhachiocephalids as well as ''Oudenodon'', ''Tropidostoma'', and other oudenodontids. Overall, the relatively small ''Bulbasaurus'' provides evidence that the growth sequence of large geikiids such as ''Aulacephalodon'' did not develop along with their size, but rather was already present ancestrally and was retained as geikiids grew.

Classification

In 2017, ''Bulbasaurus'' was assigned to the Geikiidae clade of dicynodonts on account of its prominent nasal-frontal ridge, its relatively wide interorbital region, and its twisted squamosal on the postorbital bar. This assignment was supported by a phylogenetic analysis based on that conducted by Kammerer ''et al.'' in 2011, which found it as the closest relative of ''Aulacephalodon'' on the basis of it lacking a ridge behind its tusk (which is ontogenetically influenced). However, this assignment is somewhat questionable, and forcing ''Bulbasaurus'' as a basal geikiid outside of the Geikiinae (''Aulacephalodon'', '' Geikia'', and ''Pelanomodon'') only requires one additional evolutionary step. Overall, the Cryptodontia (including the Geikiidae) were very unstable, suggesting that current datasets may not be able to sufficiently evaluate their relationships. An excerpt from the consensus of two phylogenetic trees, illustrating the relationships between cryptodontians, is shown below.

''Tropidostoma'', the genus ''Bulbasaurus'' was originally assigned to, exhibits two distinct morphologies - a robust morph with short snout and large tusks, and a gracile morph with long snout and small tusks, which probably represents sexual dimorphism as in other dicynodonts. However, ''Bulbasaurus'' matches neither of those morphologies; it differs from the genus ''Tropidostoma'' as a whole in many respects (addressed above). Additionally, even the holotype of ''Tropidostoma'' (which is probably immature judging by the unerupted tusks) is larger than adult specimens of ''Bulbasaurus'', which further warrants their separation. The same is true of ''Bulbasaurus'' and ''Aulacephalodon'', in addition to their differing boss morphologies and different interorbital widths. ''Bulbasaurus'' also differs from the problematic specimens BP/1/763 (assigned once to its own genus, ''Proaulacocephalodon'', or to a juvenile ''Aulacephalodon'') and TM 1480 (assigned once to '' Dicynodon hartzenbergi'') by its larger tusks and wider interorbital region, among other characteristics. These specimens are additionally from the younger ''Cistecephalus'' assemblage zone.

Paleoecology

Although the ''Tropidostoma'' Assemblage Zone, from where ''Bulbasaurus'' hails, is named after the oudenodontid ''Tropidostoma'', ''Tropidostoma'' is only the third most common dicynodont in this assemblage zone. Most common is the small '' Diictodon'', over 2000 specimens of which are known from the ''Tropidostoma'' AZ alone. Also more common than ''Tropidostoma'' is ''Pristerodon''. Other dicynodonts present include '' Cistecephalus'', '' Dicynodontoides'', '' Emydops'', ''Endothiodon'', ''Oudenodon'', '' Palemydops'', and ''Rhachiocephalus''. Notable in the ''Tropidostoma'' AZ is the lack of geikiid and dicynodontoid dicynodonts (''Dicynodontoides'' is a diictodont), which is unusual since they must have already diverged from their ancestral lineages by this time; ''Bulbasaurus'' happens to fill the former gap.

The ''Tropidostoma'' AZ also records the gradual diversification of therocephalians and gorgonopsians. Therocephalians present include '' Hofmeyria'', ''Ictidosuchoides'' (most common), ''Ictidosuchops'', ''Ictidosuchus'', and ''Lycideops''; gorgonopsids present include '' Aelurognathus'', ''Aelurosaurus'', ''Aloposaurus'', ''Cyonosaurus'', '' Gorgonops'' (most common), '' Lycaenops'', and '' Scymnognathus''. Within the Karoo Supergroup, cynodonts also first appear within the ''Tropidostoma'' AZ; they include '' Abdalodon'' (formerly assigned to '' Procynosuchus'') and '' Charassognathus''. Rarer members of the ''Tropidostoma'' AZ assemblage include the burnetiamorphs ''Lobalopex'' and ''Lophorhinus''; parareptiles '' Pareiasaurus'' and ''Saurorictus''; the archosauromorph '' Younginia''; and the temnospondyl '' Rhinesuchus''.

''Bulbasaurus'' was probably buried on floodplains surrounding a meandering river up to wide and with point bars up to in diameter. This river flowed from the southern mountains northeast onto an alluvial fan some wide. The water flow in the rivers was seasonally dependent, but there was probably flowing water year-round. About every 30,000 years, the river banks were breached by flooding, leaving overbank deposits and a series of small, isolated ponds.

References

{{Taxonbar, from=Q28647194

Dicynodonts
Lopingian synapsids of Africa
Permian South Africa
Fossils of South Africa
Fossil taxa described in 2017
Anomodont genera
Monotypic vertebrate genera