''Tetragonias'' is an extinct
genus
Genus ( plural genera ) is a taxonomic rank used in the biological classification of extant taxon, living and fossil organisms as well as Virus classification#ICTV classification, viruses. In the hierarchy of biological classification, genus com ...
of
dicynodont
Dicynodontia is an extinct clade of anomodonts, an extinct type of non-mammalian therapsid. Dicynodonts were herbivorous animals with a pair of tusks, hence their name, which means 'two dog tooth'. Members of the group possessed a horny, typicall ...
from the
Anisian
In the geologic timescale, the Anisian is the lower stage or earliest age of the Middle Triassic series or epoch and lasted from million years ago until million years ago. The Anisian Age succeeds the Olenekian Age (part of the Lower Triassic Ep ...
Manda Beds of
Tanzania
Tanzania (; ), officially the United Republic of Tanzania ( sw, Jamhuri ya Muungano wa Tanzania), is a country in East Africa within the African Great Lakes region. It borders Uganda to the north; Kenya to the northeast; Comoro Islands and ...
. With ''tetra'' meaning “four,” and ''goni'' meaning “angle,” the name references the square shape of the ''Tetragonias'' skull when viewed dorsally.
Not to be confused with the plant ''
Tetragonia
''Tetragonia'' is a genus of about 85 species of flowering plants in the family Aizoaceae, native to temperate and subtropical regions mostly of the Southern Hemisphere, in New Zealand, Australia
Australia, officially the Commonwealth ...
,'' ''Tetragonias'' were dicynodont anomodonts discovered in the late 1960s by paleontologist A. R. I. Cruickshank in the Manda Formation. Only the type species, ''T. njalilus'', has been recognized.
Originally thought to have existed during the lower Middle Triassic age, also called the
Anisian
In the geologic timescale, the Anisian is the lower stage or earliest age of the Middle Triassic series or epoch and lasted from million years ago until million years ago. The Anisian Age succeeds the Olenekian Age (part of the Lower Triassic Ep ...
age, Gay and Cruickshank (1999) later postulated that the Manda Formation may have actually been of the Ladinian age. This terrestrial herbivore was determined to have relation to the genera Lystrosaurus and Kannemeyeria.
Discovery and historical information
Initially described by
F. von Huene in 1942 as ''Dicynodon njalilus'', Cruickshank renamed this species ''Tetragonias njalilus'' to correctly point out how different the palate and intertemporal bar structures of this Triassic creature were from the other mostly Permian dicynodonts. He mainly aimed to revise the earlier von Huene descriptions of the skull and postcranial skeleton. Cruickshank's contribution to the scientific classification for ''Tetragonias'' is what is used today, although, there have been questions as of late concerning the "taxonomic integrity" of ''Tetragonias'' due of Cruickshank's misattribution of certain size differences in features to sexual dimorphism as opposed to feeding differences or other taxa.
Description and paleobiology
As for Cruickshank's specific diagnosis, ''T. njalilus'' was described as a “medium sized dicynodont, tusked in both sexes" with an overall rectangular skull shape in dorsal view. He included details about the maxillary processes surrounding the tusks differently in males and females, the fact that the postorbital bones do not meet the squamosals at the back of the temporal fenestrae, information about the size of the interpterygoid space in relation to the length of the internal nares, and most significantly, that the intertemporal bar is “drawn out into low parietal crest.”
Skull
''T. njalilus'' skull bones are quite large. One notable feature is the “sharply downturned snout,” which inspired the hypothesis of possible relation to the genus ''Lystrosaurus''. However, ''T. njalilus'' has much larger temporal fenestrae than ''Lystrosaurus'' ''murrayi'', as well as a shallower skull, no postfrontals, a parietal crest, and differences in size of some parts of the palate. The postorbitals don't cover the parietals to the same degree as von Huene had described, and as mentioned before, do not meet the squamosals.
The palatal openings to the internal nares of Triassic dicynodonts are significantly larger than the palatal openings of Permian dicynodonts, which is a consistent pattern that have prompted some have tried to explain using the idea that concentrations of atmospheric oxygen have been gradually declining and contributed to end-Permian extinction.
Postcranial skeleton
Pelvic girdle and locomotion
![Phylogenetic-relationships-of-higher-taxonomic-groups-with-the-Dicynodontia-The](https://upload.wikimedia.org/wikipedia/commons/6/66/Phylogenetic-relationships-of-higher-taxonomic-groups-with-the-Dicynodontia-The.png)
To further expound on the posture of the ''Tetragonias'' pelvic girdle, the iliac blade forms a ventromedial angle with the ischium and the pubis. All the pelvic bones in the acetabulum are fused. There is a curvature in the pelvis of ''Tetragonias'' that causes the pubis and ischium to extend far medially and ventrally (see Fig. 4 of Fröbisch). This causes the iliac blade to form the major vertical component of the pelvic bone, which contrasts with what Cruickshank's 1967 paper suggests. It appears there was a misinterpretation about the entire pelvis being vertical.
In ''Tetragonias'' the straight medial margins of the puboischiadic suggest an articulation which is supported by ligaments or cartilage, although there's no evidence for a suture or fusion along the midline. All pelvic bones in the holotype of ''T. njalilus'' at both the left and right sides of the pelvic girdle of are fused. This indicates that movement b/n the pelvic bones of one body side was impossible (in the mature animal). The pelvis is separated into a vertically & a more horizontally oriented part. It possesses an upward-arched backbone, though less pronounced than Cruickshank had postulated.
As mentioned earlier concerning the biomechanical strain on the hind limb, most of ''Tetragonias's'' body weight would have been carried by the adducted hind limb rather than pelvis: “In this orientation of the pelvic girdle, the supraacetabular crest is strongly overhanging the acetabulum, forming a well-developed dorsal roof to the laterally pointing articulation surface. This feature emphasizes a direct transmission of the body load from the pelvis to the femur, resulting in a more adducted position of the hind limb.”
This inhibits ''Tetragonias'' from sprawling motion, but rather, a parasaggital gait.
Vertebrae
Most synapsids possess only 3 sacral vertebrae, which articulate with the ilium and are vital in tetrapod locomotion. According to Griffin et al., “The ancestral synapsid probably possessed two sacral vertebrae (Romer 1956; LeBlanc and Reisz 2014), with Therapsida and some non-therapsid lineages (e.g.,
Caseidae
Caseidae are an extinct family of basal synapsids that lived from the Late Carboniferous to Middle Permian between about 300 and 265 million years ago. Fossils of these animals come from the south-central part of the United States (Texas, Oklaho ...
,
Edaphosauridae,
Sphenacodontidae) incorporating a third sacral from the caudal series.”
Synapsids display very little variation in the number of presacral vertebrae, as their axial column is highly conserved. However, Dicynodontia, including ''T. njalilus'', is an exception, containing a clade of anomodont therapsids with far greater variation in morphology. These amonodonts can possess up to seven or even more sacral vertebrae, which is quite the deviation from its therapsid relatives. This is likely attributable to the trend of growing body size observed throughout dicynodont evolutionary history, which positively correlates with an increase in sacral vertebrae number. This has also led to a wide-ranging variety of body sizes. These sacral vertebrae are used as a key identifying feature in ''Tetragonias'' phylogeny.
Researchers hypothesize that dicynodonts that increased their number of sacral vertebrae from three to four achieved this by adding a novel fourth vertebrae anteriorly to the other three, which make up the plesiomorphic sacrum. (Griffin) As for taxa with more than four sacral vertebrae, they essentially follow the same body plan in that there are “three plesiomorphic sacrals...in addition to one or more novel vertebrae...(see Figs. 1, 2)...Taken together, our observations indicate that all dicynodonts with a given sacral count appear to possess identically constructed sacra...Most novel sacral vertebrae are added anteriorly to the plesiomorphic sacrum in dicynodonts, with only one vertebra added posteriorly.”
Other features
The basicranium of most Triassic dicynodonts shortens compared to those of the Permian. However, ''Tetragonias'' and a few other genera actually maintain the same basicranial length as Permian dicynodonts.
Geological and paleoenvironmental information
The Manda Formation, also known as Manda Beds, is a geological formation located in the southern region of Tanzania in the Ruhuhu Basin. The formation is made primarily of sandstone but also consists of siltstone and mudstone.
![Journal](https://upload.wikimedia.org/wikipedia/commons/9/9a/Journal.pone.0072753.g001.png)
At the time of his 1967 publishing, Cruickshank hypothesized that the Manda Formation was of the Middle Triassic age and also made mention that some parts of the Manda Beds were understood to be the stratigraphic equivalent of the Molteno Beds of South Africa. This latter piece of information was due to the fact that Kannemeyeria latifrons, which existed during the Lower Triassic Cynognathus-zone, occurred in both formations.
References
External links
The main groups of non-mammalian synapsids at Mikko's Phylogeny Archive
{{Taxonbar, from=Q2309862
Dicynodonts
Anisian life
Middle Triassic synapsids of Africa
Triassic Tanzania
Fossils of Tanzania
Fossil taxa described in 1967
Anomodont genera