Biology:Diplocynodon
Diplocynodon is an extinct genus of eusuchian, either an alligatoroid crocodilian or a stem-group crocodilian, that lived during the Paleocene to Middle Miocene in Europe. Some species may have reached lengths of 3 metres (9.8 ft),[1] while others probably did not exceed 1 metre (3.3 ft).[2] They are almost exclusively found in freshwater environments.[3] The various species are thought to have been opportunistic aquatic predators.[4]
In the nineteenth century, D. steineri was named from Styria, Austria and D. styriacus was named from Austria and France. A third Austrian species, Enneodon ungeri, was placed in its own genus. The Austrian and French species of Diplocynodon were synonymized with E. ungeri in 2011, and because the name Diplocynodon has priority over Enneodon, the species is now called D. ungeri.[5] Other genera have recently been found to be synonymous with Diplocynodon. Hispanochampsa muelleri of Spain was determined to be synonymous with Diplocynodon in 2006,[6] and Baryphracta deponaie of Germany was confirmed to be synonymous with Diplocynodon in 2012.[7]
Well preserved specimens have been found in the Messel Pit and the Geiseltal lignite deposit in Germany. Most articulated Diplocynodon specimens from these localities contain gastroliths. In the Eocene epoch, the German sites were either a swampy freshwater lake (Messel Pit) or a peat bog swamp (Geiseltal).
Species
| Species | |||||
|---|---|---|---|---|---|
| Species | Age | Location | Unit | Notes | Images |
|
D. darwini |
|
Messel pit |
All specimens are from Messel pit of Germany. Synonyms are: D. ebertsi and D. hallense. |
||
|
Middle Eocene |
|
Messel pit |
Synonyms are: Baryphracta deponaie. | ||
|
D. elavericus[9] |
Middle Priabonian |
|
Domérat |
All specimens came from Allier, Massif Central of France. | |
|
D. gervaisi |
Earliest Rupelian |
|
Ronzon |
Synonyms are: Saurocainus gervaisi. | |
|
D. hantoniensis |
Early Priabonian |
|
All specimens came from Hordwell, southern England. D. cf. hantoniensis is known from the Oligocene of Dordogne, France. | ||
| D. levantinicum[1] | Oligocene (Chattian) | Maritsa Formation | |||
|
D. kochi |
Eocene (Priabonian) |
|
Cluj Limestone Formation |
||
|
D. muelleri[6] |
Middle Rupelian |
|
El Talladell |
More than 100 are known, all from Lleida Province, Catalonia. Synonyms are: Hispanochampsa muelleri, D. guerini and D. marini. | |
|
D. ratelii |
|
|
Saint-Gérand-le-Puy* |
D. ratelii is the type species of Diplocynodon. Most of the specimens came from Allier, Massif Central of France. Synonyms are: D. gracile. | |
|
D. tormis |
Late Bartonian |
|
Salamanca |
||
|
D. ungeri[5] |
Middle Miocene |
|
|
Synonyms are: Enneodon ungeri, D. steineri, and D. styriacus (see text). | |
*Locality and/or horizon of the type specimen.
Phylogeny
Diplocynodon is one of the basal-most members of the superfamily Alligatoroidea. Diplocynodon's placement within Alligatoroidea can be shown in the cladogram below, based on a 2018 tip dating study by Lee & Yates that simultaneously used morphological, molecular (DNA sequencing), and stratigraphic (fossil age) data.[10]
| Crocodylia |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Below is a more detailed cladogram of Diplocynodon:[11]
| Diplocynodon |
| ||||||||||||||||||||||||
In a 2025 study, Jules D. Walter and colleagues argue that many character states previously thought to be diagnostic for alligatoroids were actually much more widespread. In their analysis several genera traditionally viewed as basal alligatoroids, among them Diplocynodon, were found to not only fall outside of Alligatoroidea but to not even be true crocodilians, instead representing derived non-crocodilian eusuchians.[12]
Palaeobiology
Osteohistological analysis of D. hantoniensis suggests that it had a similar pattern of growth to the modern American alligator, exhibiting a determinate, seasonally-controlled rate of growth. Additionally, D. hantoniensis was allometrically very similar to American alligators, with the femoral length and femoral circumference scaling in a similar fashion in both species.[13]
CT scans of D. tormis reconstruct internal structures of its snout and a portion of its brain, with implications for its sensory and cognitive capabilities. The relative sizes of the olfactory bulbs overlap with alligatoroids and fall short of true crocodiles, adding to anatomical evidence for a closer relationship to alligatoroids. The optic lobes and reptile encephalization quotient are proportionally smaller than other medium-sized crocodilians, though this could be influenced by incomplete preservation at the back of the skull.[14]
Palaeoecology
Based on skull shape analysis of the crocodylians known from the Lutetian site of Geiseltal, Diplocynodon was a small generalist carnivore that partitioned its resources with the larger Asiatosuchus.[15] According to enamel δ13C values from specimens from the Late Oligocene site of Enspel, the Diplocynodon living in the palaeoenvironment fed primarily on aquatic vertebrates.[16]
References
- ↑ 1.0 1.1 Massonne, Tobias; Böhme, Madelaine (2022-11-09). "Re-evaluation of the morphology and phylogeny of Diplocynodon levantinicum Huene & Nikoloff, 1963 and the stratigraphic age of the West Maritsa coal field (Upper Thrace Basin, Bulgaria)" (in en). PeerJ 10. doi:10.7717/peerj.14167. ISSN 2167-8359. PMID 36389401.
- ↑ Delfino, Massimo; Smith, Thierry (November 2012). "Reappraisal of the morphology and phylogenetic relationships of the middle Eocene alligatoroid Diplocynodon deponiae (Frey, Laemmert, and Riess, 1987) based on a three-dimensional specimen" (in en). Journal of Vertebrate Paleontology 32 (6): 1358–1369. doi:10.1080/02724634.2012.699484. ISSN 0272-4634. Bibcode: 2012JVPal..32.1358D. http://www.tandfonline.com/doi/abs/10.1080/02724634.2012.699484.
- ↑ Sabău I, Venczel M, Codrea VA, Bordeianu M. 2021. Diplocynodon: a salt water eocene crocodile from Transylvania? North-Western Journal of Zoology 17(1):117-121
- ↑ Tütken, Thomas; Absolon, Julia (March 2015). "Late Oligocene ambient temperatures reconstructed by stable isotope analysis of terrestrial and aquatic vertebrate fossils of Enspel, Germany" (in en). Palaeobiodiversity and Palaeoenvironments 95 (1): 17–31. doi:10.1007/s12549-014-0183-7. ISSN 1867-1594. Bibcode: 2015PdPe...95...17T. http://link.springer.com/10.1007/s12549-014-0183-7.
- ↑ 5.0 5.1 Jeremy E. Martin; Martin Gross (2011). "Taxonomic clarification of Diplocynodon Pomel, 1847 (Crocodilia) from the Miocene of Styria, Austria". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen 261 (2): 177–193. doi:10.1127/0077-7749/2011/0159.
- ↑ 6.0 6.1 Cite error: Invalid
<ref>tag; no text was provided for refs namedHispanochampsa - ↑ 7.0 7.1 Cite error: Invalid
<ref>tag; no text was provided for refs namedBaryphracta - ↑ Cite error: Invalid
<ref>tag; no text was provided for refs namedRossman - ↑ Jeremy E. Martin (2010). "A new species of Diplocynodon (Crocodylia, Alligatoroidea) from the Late Eocene of the Massif Central, France, and the evolution of the genus in the climatic context of the Late Palaeogene". Geological Magazine 147 (4): 596–610. doi:10.1017/S0016756809990161. Bibcode: 2010GeoM..147..596M.
- ↑ Michael S. Y. Lee; Adam M. Yates (27 June 2018). "Tip-dating and homoplasy: reconciling the shallow molecular divergences of modern gharials with their long fossil". Proceedings of the Royal Society B 285 (1881). doi:10.1098/rspb.2018.1071. PMID 30051855.
- ↑ Tobias Massonne; Davit Vasilyan; Márton Rabi; Madelaine Böhme (2019). "A new alligatoroid from the Eocene of Vietnam highlights an extinct Asian clade independent from extant Alligator sinensis". PeerJ 7. doi:10.7717/peerj.7562. PMID 31720094.
- ↑ Walter, J. D.; Massonne, T.; Paiva, A. L. S.; Martin, J. E.; Delfino, M.; Rabi, M. (2025). "Expanded phylogeny elucidates Deinosuchus relationships, crocodylian osmoregulation and body-size evolution". Communications Biology 8: 611. doi:10.1038/s42003-025-07653-4.
- ↑ Hoffman, D. K.; Goldsmith, E. R.; Houssaye, A.; Maidment, S. C. R.; Felice, R. N.; Mannion, Philip D. (9 February 2025). "Evolution of growth strategy in alligators and caimans informed by osteohistology of the late Eocene early-diverging alligatoroid crocodylian Diplocynodon hantoniensis" (in en). Journal of Anatomy. doi:10.1111/joa.14231. ISSN 0021-8782. PMID 39924872.
- ↑ Serrano-Martínez, Alejandro; Luján, Àngel H.; García-Pérez, Ángel; Fortuny, Josep (2025-02-24). "New data on the inner skull cavities of Diplocynodon tormis (Crocodylia, Diplocynodontinae) from the Duero Basin (Iberian Peninsula, Spain)" (in en). Fossil Record 28 (1): 67–77. doi:10.3897/fr.28.133743. ISSN 2193-0074. https://fr.pensoft.net/article/133743/.
- ↑ Hastings, Alexander K.; Hellmund, Meinolf (January 2017). "Evidence for prey preference partitioning in the middle Eocene high-diversity crocodylian assemblage of the Geiseltal-Fossillagerstätte, Germany utilizing skull shape analysis" (in en). Geological Magazine 154 (1): 119–146. doi:10.1017/S0016756815001041. ISSN 0016-7568. Bibcode: 2017GeoM..154..119H. https://www.cambridge.org/core/journals/geological-magazine/article/abs/evidence-for-prey-preference-partitioning-in-the-middle-eocene-highdiversity-crocodylian-assemblage-of-the-geiseltalfossillagerstatte-germany-utilizing-skull-shape-analysis/717771502180E87AA6FE3E8966955D72. Retrieved 19 February 2025.
- ↑ Tütken, Thomas; Absolon, Julia (12 February 2015). "Late Oligocene ambient temperatures reconstructed by stable isotope analysis of terrestrial and aquatic vertebrate fossils of Enspel, Germany" (in en). Palaeobiodiversity and Palaeoenvironments 95 (1): 17–31. doi:10.1007/s12549-014-0183-7. ISSN 1867-1594. Bibcode: 2015PdPe...95...17T. https://link.springer.com/article/10.1007/s12549-014-0183-7. Retrieved 23 December 2024.
- Fossils (Smithsonian Handbooks) by David Ward (Page 243)
External links
Template:Extinct Crocodilia Wikidata ☰ Q13797209 entry

