Yesterday Pardo et al. 2017
described two conspecific and incomplete amphibians in the lineage of caecilians, Chinlestegophis jerkinsi (DMNH 56658, DMNH 39033, Figs. 1, 3). These long-sought specimens were discovered in the late 1990s preserved in Late Triassic burrows.
This is really big news!
Congratulations to the Pardo team!!
From the abstract:
“Here, we report on a small amphibian from the Upper Triassic of Colorado, United States, with a mélange of caecilian synapomorphies and general lissamphibian plesiomorphies. We evaluated its relationships by designing an inclusive phylogenetic analysis that broadly incorporates definitive members of the modern lissamphibian orders and a diversity of extinct temnospondyl amphibians, including stereospondyls. Stem caecilian morphology reveals a previously unrecognized stepwise acquisition of typical caecilian cranial apomorphies during the Triassic. A major implication is that many Paleozoic total group lissamphibians (i.e., higher temnospondyls, including the stereospondyl subclade) fall within crown Lissamphibia, which must have originated before 315 million years ago.”
“Small stereospondyl with a combination of brachyopoid and caecilian characteristics.” Stereospondyls were generally large, flat-skulled aquatic taxa that had simplified and rather weak vertebrae in which the intercentrum was topped by a neural arch and the pleurocentrum was reduced to absent. According to Wikipedia, “All lepospondyls have simple, spool-shaped vertebrae that did not ossify from cartilage, but rather grew as bony cylinders around the notochord.”
This is the opposite of
Reptilomorphs, in which the pleurocentra are large and the intercentra are smaller. Reptilomorphs generally were smaller and better adapted to terrestrial environments.
In the LRT traditional stereospondyls
(Fig. 5, pink) are mid-sized basalmost tetrapods, aquatic with a weak backbone because they are not far from fish with fins. Temnospondyls have stronger limbs and stronger backbones (Fig. 5, yellow), but typically remain large and aquatic.
(Fig. 5, orange) tend to be smaller with stronger limbs and vertebrae and reduce their dependence on water. Both lepospondyls (including living amphibians) and reptiles arise from this clade in the LRT.
were included in the Pardo et al study (Fig. 4) and the topology of their tree is very different from the present topology. Caecilians nest with lepospondyl microsaurs in the large reptile tree (LRT, 2014).
several skull bones are identified differently here (Fig. 1) than in the Pardo et al. study (Fig. 3). Pardo et al. identify an otic notch (that hole in the temporal region). Here that appears to be the space left open after the supratemporal has popped out during taphonomy. The supraorbital bones are all re-identified and both the lacrimal and quadratojugal are now listed in the present identification of bones. Based on conversations with Pardo and others, bone identification on several taxa may be the cause of the differing tree topologies.
Outgroup taxa should help identify the bones.
Pardo et al. recover Rileymillerus and Batrachosuchus as outgroup taxa within a large clade that includes Eryops and Sclerocephalosaurus at one base and Trimerorhachis and Greererpeton at the very base. By contrast, the LRT recovers Microbrachis and ultimately Utegenia as outgroup taxa. Microsaurs, Microbrachis and Utegenia were not mentioned in the Pardo et al. report.
First step: Learn about Rileymillerus
As usual, I knew nothing about this taxon earlier this week. Now, according to the LRT Rileymillerus nests with Oestocephalus and Ophiderpeton, two other long-bodied microsaurs with round cross-section skulls, not included in the Pardo et all study. The apparent loss or lack of bones in the temporal region may be homologous with the lateral temporal fenestra in Ophiderpeton. That’s a rare trait among basal tetrapods.
Pardo et al. excluded most of the taxa that the LRT found were most closely related to the clade Chinlestephos + (caecilians + lysorophians) That includes Microbrachis and the rest of the microsaurs. They had good reason for doing so (see below).
The Pardo et al. skull bone labels
differ from the present interpretation (Fig. 3). Even with such massive dissonance, Pardo et al. and the LRT both nest Chinlestegophis with caecilians and not far from Rileymillerus.
How can such a thing happen??
I can’t answer that at present. It’s frankly surprising.
The drifting of the postorbital
In most tetrapods the postorbital is one of the circumorbital bones. In caecilians and their relatives the postfrontal takes over that spot and the postorbital drifts posteriorly, still lateral to the parietal. This observation may be one of the issues attending circumorbital and temporal bone identification arguments in this clade.
In their Supplemental Info
Pardo et al. added the traits for Chinlestegophis to the dataset of Maddin et al. 2012 (who earlier described Jurassic Eocaecilia) and found Chinlestegophis nested with Rileymillerus, close to the stem frog Micromelerpeton and strong-legged Acheloma all far from the caecilians and all derived from a sister to giant Eryops. This study did include microsaurs. Lots of them! Other mismatches include nesting the large reptile Limnoscelis between Seymouria and tiny Utaherpeton and Microbrachis, taxa that share few traits with each other in the LRT. Numerous other morphological mismatches also occur In Maddin et al. Evidently no one is using scaled reconstructions in their analyses as a final check on these mismatches. In the LRT caecilians nest with similar long-bodied, tiny-limbed taxa, which some claim is due to convergence. On a similar note, the LRT lumped and separated snakes from amphisbaenids while other trees failed to do this. So perhaps convergence is not the reason here when dealing with burrowing amphibians.
A note from Jason Pardo
restates that the Maddin et al. study “found no close relationship between Eocaecilia and lepospondyls nor did we find a close relationship between Chinlestegophis and those taxa.”
All three cladograms
share few major branches in common. As everyone knows by now, the major branches are the more difficult ones to determine. And, if we can’t agree on the identify of the skull bones, of specimens, the tree topologies will have a hard time finding consensus.
“Currently, the three prevailing theories of lissamphibian (extant amphibians) origin are:
- Monophyletic within the temnospondyli
- Monophyletic within lepospondyli
- Diphyletic (two separate ancestries) with apodans (=caecilians) within the lepospondyls and salamanders and frogs within the temnospondyli.”
So… even the experts have not come to a consensus
on basal tetrapod topologies. The LRT agrees that the lissamphibia are monophyletic within the lepospondyli, matching option #2 above. There are many aspects of caecilians that need to be interpreted in light of their phylogeny. And we’re not coming to a consensus on that. Earlier we looked at the fusion of the cheek bones in caecilians here with the extant taxon Dermophis.
Bolt JR and Chatterjee S 2000. A New Temnospondyl Amphibian from the Late Triassic of Texas. Journal of Paleontology 74(4):670-683.
Maddin HC, Jenkins FA, Jr, Anderson JS 2012. The braincase of Eocaecilia micro podia (Lissamphibia, Gymnophiona) and the origin of Caecilians. PLoS One 7:e50743.
Pardo JD, Small BJ and Huttenlocker AK. 2017, Stem caecilian from the Triassic of Colorado sheds light on the origins of Lissamphibia. PNAS: 7 pp. www.pnas.org/cgi/doi/10.1073/pnas.1706752114