Biology:Edaphosauridae

From HandWiki

Edaphosauridae is a family of mostly large (up to 3 m (9.8 ft) or more) Late Carboniferous to Early Permian synapsids. Edaphosaur fossils are so far known only from North America and Europe. Edaphosaurids transitioned from being small carnivores in their most primitive members into some of the earliest large terrestrial herbivores. They are noted for their neural spine sails on their backs, which unlike those of Dimetrodon exhibit distinctive outwards facing growths.

Characteristics

Skull and lower jaw of Edaphosaurus, showing the development of a battery of palatal teeth on the pterygoid, ectopterygoid and palatine bones, along with a corresponding interlocking battery on the lower jaw, used to grind high fiber plant material
Size of Ianthasaurus compared to a human hand
Size of various Edaphosaurus species compared to a human

Edaphosaurids saw a transition from being small insectivores/carnivores in the most primitive members of the group like Ianthasaurus, towards being large specialised herbivores in later members of the group like Edaphosaurus. They were the earliest known herbivorous amniotes and, along with the Diadectidae, the earliest known herbivorous tetrapods.[1] The palatal dentition on the roof of the mouth changed from being relatively unspecialised in early members like Ianthasaurus, towards being modified into specialised raised batteries, which interlocked with a similar battery on the lower jaw in Edaphosaurus, which served to grind plant material.[1][2] The upper surface of the body has a large neural spine sail formed from elongated neural spines of the back vertebrae, with this sail having varied from semi-circular to sloping at the front.[3] The neural spines at the front of the sail generally lean forwards (anteriorly), while those towards the back of the sail lean posteriorly.[4] The elongate neural spines of the sail had laterally (facing directly outwards to the side) directed tuberculate growths, unlike the neural spines of sphenacodontids like Dimetrodon. These tubercules vary considerably in the patterns of their arrangement between edaphosaurid species. The purpose of the sail is unknown, but have been variously suggested to have served for thermoregulation (though the supporting evidence for this has been criticised), defense, individual/species recognition, and/or display for intraspecific competition.[5]

Classification

The interrelationships of Edaphosauridae was investigated in details by David M. Mazierski and Robert R. Reisz (2010). The cladogram below is modified after their phylogenetic analysis.[6]

Edaphosauridae
 

Ianthasaurus hardestiorum

 
 
 

Glaucosaurus megalops

 
 

Lupeosaurus kayi

 
 
 

Edaphosaurus novomexicanus

 
 
 

Edaphosaurus colohistion

 
 
 

Edaphosaurus boanerges

 
 
 

Edaphosaurus cruciger

 
 

Edaphosaurus pogonias

 
 
 
 
 
 
 

Edaphosauridae is generally placed as closely related to Sphenacodontia as part of the clade Sphenacomorpha.[7] Below is a cladogram modified from the analysis of Benson (2012):[8]

 
 

Tseajaia campi

 
 

Limnoscelis paludis

 
Amniota
 
 

Captorhinus spp.

 
 

Protorothyris archeri

 
 
Synapsida
 
 

Ophiacodontidae

 
 

Varanopidae

 
 
 
 

Caseasauria

 
 
 

Ianthodon schultzei

 
 
Edaphosauridae
 

Ianthasaurus hardestiorum

 
 
 

Glaucosaurus megalops

 
 

Lupeosaurus kayi

 
 
 

Edaphosaurus boanerges

 
 

Edaphosaurus novomexicanus

 
 
 
 
Sphenacodontia
 

Haptodus garnettensis

 
 
 

Pantelosaurus saxonicus

 
 
 

Therapsida

 
 

Sphenacodontidae

 
 
 
 
 
 
 
 
 
 

References

  1. ↑ 1.0 1.1 Mann, Arjan; Henrici, Amy C.; Sues, Hans-Dieter; Pierce, Stephanie E. (2023). "A new Carboniferous edaphosaurid and the origin of herbivory in mammal forerunners". Scientific Reports 13 (1). doi:10.1038/s41598-023-30626-8. PMID 37019927. Bibcode: 2023NatSR..13.4459M. 
  2. ↑ Modesto SP (1995) The skull of the herbivorous synapsid Edaphosaurus boanerges from the Lower Permian of Texas. Palaeontology 38, 213–239.
  3. ↑ Spencer G., Lucas; Rinehart, Larry; Celeskey, Matthew D. (November 2018). "The oldest specialized tetrapod herbivore: A new eupelycosaur from the Permian of New Mexico, USA". Palaeontologia Electronica 21.3.39A (3): 899. doi:10.26879/899. Bibcode: 2018PalEl..21..899L. 
  4. ↑ "Autapomorphies of the main clades of synapsids". http://tolweb.org/notes/?note_id=466. 
  5. ↑ Huttenlocker, Adam K.; Mazierski, David; Reisz, Robert R. (May 2011). "Comparative osteohistology of hyperelongate neural spines in the Edaphosauridae (Amniota: Synapsida)" (in en). Palaeontology 54 (3): 573–590. doi:10.1111/j.1475-4983.2011.01047.x. ISSN 0031-0239. Bibcode: 2011Palgy..54..573H. https://onlinelibrary.wiley.com/doi/10.1111/j.1475-4983.2011.01047.x. 
  6. ↑ Mazierski, David M.; Reisz, Robert R. (2010). "Description of a new specimen of Ianthasaurus hardestiorum (Eupelycosauria: Edaphosauridae) and a re-evaluation of edaphosaurid phylogeny". Journal of Vertebrate Paleontology 47 (6): 901–912. doi:10.1139/E10-017. Bibcode: 2010CaJES..47..901M. 
  7. ↑ Huttenlocker, Adam K.; Singh, Suresh A.; Henrici, Amy C.; Sumida, Stuart S. (December 2021). "A Carboniferous synapsid with caniniform teeth and a reappraisal of mandibular size-shape heterodonty in the origin of mammals". Royal Society Open Science 8 (12). doi:10.1098/rsos.211237. ISSN 2054-5703. PMID 34925870. Bibcode: 2021RSOS....811237H. 
  8. ↑ Benson, R.J. (2012). "Interrelationships of basal synapsids: cranial and postcranial morphological partitions suggest different topologies". Journal of Systematic Palaeontology 10 (4): 601–624. doi:10.1080/14772019.2011.631042. Bibcode: 2012JSPal..10..601B. 
  • Carroll, R. L. (1988), Vertebrate Paleontology and Evolution, WH Freeman & Co.
  • Reisz, R. R., 1986, Handbuch der Paläoherpetologie – Encyclopedia of Paleoherpetology, Part 17A Pelycosauria Verlag Dr. Friedrich Pfeil, ISBN 3-89937-032-5

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