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Mammuthus meridionalis

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Mammuthus meridionalis
Temporal range: 2.5–0.8 Ma
↓
 Early Pleistocene
Mounted skeleton of the Durfort mammoth [fr], National Museum of Natural History, France (Muséum national d'histoire naturelle)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Proboscidea
Family: Elephantidae
Genus: †Mammuthus
Species:
†M. meridionalis
Binomial name
†Mammuthus meridionalis
(Nesti, 1825)
Synonyms
  • Archidiskodon meridionalis
  • Mammuthus gromovi (Alexeeva & Garutt, 1965)
  • Mammuthus meridionalis vestinus
  • M. m. voigtstedtensis (Dietrich, 1965)

Mammuthus meridionalis, sometimes called the southern mammoth, is an extinct species of mammoth native to Eurasia, including Europe, during the Early Pleistocene, living from around 2.5 million years ago to 800,000 years ago.

Taxonomy

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Molar

Mammuthus meridionalis was originally named by Filippo Nesti in 1825 as Elephas meridionalis based on remains collected from the Upper Valdarno region in Tuscany, Italy.[1]

The taxonomy of extinct elephants was complicated by the early 20th century, and in 1942, Henry Fairfield Osborn's posthumous monograph on the Proboscidea was published, wherein he used various taxon names that had previously been proposed for mammoth species, including replacing Mammuthus with Mammonteus, as he believed the former name to be invalidly published.[2] Mammoth taxonomy was simplified by various researchers from the 1970s onwards, all species were retained in the genus Mammuthus, and many proposed differences between species were instead interpreted as intraspecific variation.[3] The name Archidiskodon meridionalis is retained by some Russian researchers.[4][5]

Description

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Skeletal restoration of a 4 metre tall male
Complete skeleton in the Museo Nazionale d'Abruzzo, Italy

M. meridionalis was a large proboscidean, exceeding modern elephants in size.[6] A mature adult male known from a mostly complete skeleton displayed at Forte Spagnolo, L'Aquila, Italy, estimated to be approximately 3.97–4.05 m (13.0–13.3 ft) tall at the shoulder in the flesh, was volumetrically estimated to weigh 10.7–11.4 tonnes (11.8–12.6 short tons).[6][7] Such sizes are suggested to have been typical for males of this species.[6] Like modern elephants females were considerably smaller, with estimated average adult shoulder height of 3.3 m (10.8 ft) and a weight of around 7 tonnes (7.7 short tons).[8]

The skull was prominently domed, though the height of the dome was lower than later mammoth species. The head represented the highest point of the animal. The body was broad and the back was noticeably sloped. It had robust, elongated twisted tusks, common of mammoths.[8] Its molars had low crowns[9] and around 13 thick enamel ridges (lamellae) on the third molars, substantially lower than the number in later mammoth species.[10] M. meridionalis lived in relatively warm climates, which makes it more probable that it lacked dense fur.[9] The ears are also suggested to have been medium-large sized, with the tail being shorter than living elephants but longer than later mammoth species.[8]

Later European M. meridionalis populations differ from early representatives of the species by having shorter and taller skulls and mandibles, differing shapes of the temporal fossa, orbits and tusk alveoli (sockets), and an increase in the number of lamellae on the teeth and tooth crown height (hypsodonty).[11]

Ecology

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Fossilized plants found with the remains show that M. meridionalis was living in a time of mild climate, generally as warm or slightly warmer than Europe experiences today. Some populations inhabited woodlands, which included oak, ash, beech and other familiar European trees, as well as some that are now exotic to the region, such as hemlock, wing nut and hickory. Further east, discoveries at Ubeidiya (Israel) and Dmanisi (Georgia) show the early mammoth living in a partially open habitat with grassy areas.[9]

Dental microwear of the teeth of M. meridionalis suggest that the species was a variable mixed feeder, that consumed both grass and browse, with its diet varying according to local conditions,[12] with some populations exhibiting browse-dominated feeding,[13] while others grass-dominant.[12]

During the early part of its existence in Europe, it existed alongside the "tetralophodont gomphothere" Anancus arvernensis. Dietary analysis based on microwear suggests that there was niche partitioning between the two species, with M. meridonalis occupying more open habitats.[14]

Juvenile Mammuthus meridionalis have been suggested to have at least occasionally been preyed upon by the large sabertooth cat Homotherium latidens, based on isotopic analysis of specimens from the Venta Micena locality in southeast Spain.[15] Remains from the Fuente Nueva-3 site also in southeast Spain suggests that carcasses of Mammuthus meridionalis were at times scavenged on by the giant hyena Pachycrocuta.[16]

Evolution

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Since many remains of each species of mammoth are known from several localities, it is possible to reconstruct the evolutionary history of the genus through morphological studies. Mammoth species can be identified from the number of enamel ridges (or lamellar plates) on their molars: primitive species had few ridges, and the number increased gradually as new species evolved to feed on more abrasive food items. The crowns of the teeth became deeper in height and the skulls became taller to accommodate this. At the same time, the skulls became shorter from front to back to minimise the weight of the head.[17][18]

Mammuthus meridionalis is thought to descend from Mammuthus rumanus, the oldest mammoth species known outside of Africa, with the earliest records of M. meridionalis dating to around 2.6-2.5 million years ago, at the beginning of the Pleistocene.[17] Some early members of M. meridionalis spanning from 2.6-2.0 million years ago were historically assigned to the species M. gromovi, which some authors have regarded as the subspecies M. meridionalis gromovi.[17][11] A population of M. meridionalis evolved into the steppe mammoth (M. trogontherii) with 18–20 third molar ridges in eastern Asia, prior to 1.7 million years ago.[10] The Columbian mammoth (M. columbi) evolved from a population of M. trogontherii that had crossed the Bering Strait and entered North America about 1.5 million years ago, and not M. meridionalis as has been historically suggested.[10][19][20] European M. meridionalis specimens from around 2-1.7 million years ago are assigned to the subspecies M. meridionalis meridionalis. Advanced late Early Pleistocene populations of M. meridionalis in Europe, spanning from around 1.7-0.8 million years ago are assigned to the subspecies M. meridionalis vestinus (including the likely synonym M. meridionalis depereti) and M. meridionalis tamanensis. These two subspecies may be synonymous with each other.[11] Steppe mammoths replaced M. meridionalis in Europe in a diachronous mosaic pattern at the end of the Early Pleistocene, between around 1 and 0.8-0.7 million years ago, which was also co-incident with the arrival of the straight-tusked elephant (Palaeoloxodon antiquus) into Europe, which may have out-competed M. meridionalis.[17][11] During the interval of replacement, M. meridionalis and M. trogontherii may have co-existed in some localities, with rare specimens with molar morphology intermediate between the two species suggesting that there may have been hybridisation between them.[21]

The dwarf mammoth species Mammuthus creticus, which inhabited the island of Crete at some point during the Early Pleistocene to early Middle Pleistocene, is suggested to have descended from M. meridionalis.[22]

Mammuthus meridionalis reconstruction

Relationship with humans

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Remains of M. meridionalis at several sites have been found with cut marks and/or associated with stone tools, suggested to represent evidence of butchery by archaic humans.[23] A number of bones of Mammuthus meridionalis from the Dmanisi site in Georgia, dating to 1.8 million years ago have cut marks likely created by local Homo erectus.[24] At the Fuente Nueva-3 and Barranc de la Boella sites in Spain, dating to approximately 1.3 and 1-0.8 million years ago respectively, remains of M. meridionalis are associated with stone tools (in the latter site of the Acheulean type), primarily lithic flakes. At Barranc de la Boella, some rib bones possibly bear cut marks,[23] with cut marks being definitvely reported from bones found at Fuente Nueva-3.[25] These sites likely represent evidence of opportunistic scavenging, rather than active hunting.[26]

References

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  1. ^ Palombo, Maria R.; Ferretti, Marco P. (January 2005). "Elephant fossil record from Italy: knowledge, problems, and perspectives". Quaternary International. 126–128: 107–136. Bibcode:2005QuInt.126..107P. doi:10.1016/j.quaint.2004.04.018.
  2. ^ Osborn, H. F. (1942). Percy, M. R. (ed.). Proboscidea: A monograph of the discovery, evolution, migration and extinction of the mastodonts and elephants of the world. Vol. 2. New York: J. Pierpont Morgan Fund. pp. 1116–1169.
  3. ^ Maglio, V. J. (1973). "Origin and evolution of the Elephantidae". Transactions of the American Philosophical Society. 63 (3): 1–149. doi:10.2307/1379357. JSTOR 1379357.
  4. ^ Shchelinsky, V.E. (April 2020). "Large mammal hunting and use of aquatic food resources in the Early Palaeolithic (finds from Early Acheulean sites in the southern Azov Sea region)". Quaternary International. 541: 182–188. Bibcode:2020QuInt.541..182S. doi:10.1016/j.quaint.2020.04.008. S2CID 216338569.
  5. ^ Baigusheva, Vera S.; Titov, Vadim V.; Foronova, Irina V. (October 2016). "Teeth of early generations of Early Pleistocene elephants (Mammalia, Elephantidae) from Sinyaya Balka/Bogatyri site (Sea of Azov Region, Russia)". Quaternary International. 420: 306–318. Bibcode:2016QuInt.420..306B. doi:10.1016/j.quaint.2015.08.007. ISSN 1040-6182.
  6. ^ a b c Larramendi, A. (2016). "Shoulder height, body mass and shape of proboscideans" (PDF). Acta Palaeontologica Polonica. 61. doi:10.4202/app.00136.2014.
  7. ^ Romano, Marco; Manucci, Fabio; Antonelli, Matteo; Rossi, Maria Adelaide; Agostini, Silvano; Palombo, Maria Rita (2022-07-14). "In vivo restoration and volumetric body mass estimate of Mammuthus meridionalis from Madonna della Strada (Scoppito, L'Aquila)". Rivista Italiana di Paleontologia e Stratigrafia. 128 (3). doi:10.54103/2039-4942/16665. hdl:11573/1708747. ISSN 2039-4942. S2CID 250580462.
  8. ^ a b c Larramendi, Asier; Palombo, Maria Rita; Marano, Federica (2017). "Reconstructing the life appearance of a Pleistocene giant: size, shape, sexual dimorphism and ontogeny of Palaeoloxodon antiquus (Proboscidea: Elephantidae) from Neumark-Nord 1 (Germany)" (PDF). Bollettino della Società Paleontologica Italiana (3): 299–317. doi:10.4435/BSPI.2017.29 (inactive 2024-11-20). ISSN 0375-7633.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  9. ^ a b c Lister, Adrian; Bahn, Paul (2007). Mammoths: giants of the ice age. Frances Lincoln LTD. pp. 25–26. ISBN 9780711228016.
  10. ^ a b c Lister, A. M.; Sher, A. V. (2015-11-13). "Evolution and dispersal of mammoths across the Northern Hemisphere". Science. 350 (6262): 805–809. Bibcode:2015Sci...350..805L. doi:10.1126/science.aac5660. PMID 26564853. S2CID 206639522.
  11. ^ a b c d Konidaris, George E.; Kostopoulos, Dimitris S.; Koufos, George D. (2020-03-12). "Mammuthus meridionalis (Nesti, 1825) from Apollonia-1 (Mygdonia Basin, Northern Greece) and its importance within the Early Pleistocene mammoth evolution in Europe". Geodiversitas. 42 (6): 69. doi:10.5252/geodiversitas2020v42a6. ISSN 1280-9659.
  12. ^ a b Rivals, Florent; Semprebon, Gina M.; Lister, Adrian M. (September 2019). "Feeding traits and dietary variation in Pleistocene proboscideans: A tooth microwear review". Quaternary Science Reviews. 219: 145–153. Bibcode:2019QSRv..219..145R. doi:10.1016/j.quascirev.2019.06.027. S2CID 200073388.
  13. ^ Rivals, Florent; Semprebon, Gina; Lister, Adrian (26 March 2012). "An examination of dietary diversity patterns in Pleistocene proboscideans (Mammuthus, Palaeoloxodon, and Mammut) from Europe and North America as revealed by dental microwear". Quaternary International. 255: 188–195. doi:10.1016/j.quaint.2011.05.036. Retrieved 2 September 2024 – via Elsevier Science Direct.
  14. ^ Rivals, Florent; Mol, Dick; Lacombat, Frédéric; Lister, Adrian M.; Semprebon, Gina M. (2015-08-27). "Resource partitioning and niche separation between mammoths (Mammuthus rumanus and Mammuthus meridionalis) and gomphotheres (Anancus arvernensis) in the Early Pleistocene of Europe". Quaternary International. Mammoths and their Relatives: VIth International Conference, Grevena-Siatista, Greece, part 1. 379: 164–170. Bibcode:2015QuInt.379..164R. doi:10.1016/j.quaint.2014.12.031. ISSN 1040-6182.
  15. ^ Palmqvist, P.; Perez-Claros, J. A.; Janis, C. M.; Figueirido, B.; Torregrosa, V.; Grocke, D. R. (November 2008). "Biogeochemical and Ecomorphological Inferences On Prey Selection and Resource Partitioning Among Mammalian Carnivores In An Early Pleistocene Community". PALAIOS. 23 (11): 724–737. Bibcode:2008Palai..23..724P. doi:10.2110/palo.2007.p07-073r. ISSN 0883-1351.
  16. ^ Espigares, M. P.; Palmqvist, P.; Rodríguez-Ruiz, M. D.; Ros-Montoya, S.; Pérez-Ramos, A.; Rodríguez-Gómez, G.; Guerra-Merchán, A.; García-Aguilar, J. M.; Granados, A.; Campaña, I.; Martínez-Navarro, B. (2023-05-17). "Sharing food with hyenas: a latrine of Pachycrocuta brevirostris in the Early Pleistocene assemblage of Fuente Nueva-3 (Orce, Baza Basin, SE Spain)". Archaeological and Anthropological Sciences. 15 (6). doi:10.1007/s12520-023-01784-7. ISSN 1866-9557.
  17. ^ a b c d Lister, A. M.; Sher, A. V.; Van Essen, H.; Wei, G. (2005). "The pattern and process of mammoth evolution in Eurasia" (PDF). Quaternary International. 126–128: 49–64. Bibcode:2005QuInt.126...49L. doi:10.1016/j.quaint.2004.04.014.
  18. ^ Ferretti, M. P. (2003). "Structure and evolution of mammoth molar enamel". Acta Palaeontologica Polonica. 3. 48: 383–396.
  19. ^ Enk, J.; Devault, A.; Widga, C.; Saunders, J.; Szpak, P.; Southon, J.; Rouillard, J. M.; Shapiro, B.; Golding, G. B.; Zazula, G.; Froese, D.; Fisher, D. C.; MacPhee, R. D. E.; Poinar, H. (2016). "Mammuthus population dynamics in Late Pleistocene North America: divergence, phylogeography, and introgression". Frontiers in Ecology and Evolution. 4. doi:10.3389/fevo.2016.00042.
  20. ^ van der Valk, Tom; Pečnerová, Patrícia; Díez-del-Molino, David; Bergström, Anders; Oppenheimer, Jonas; Hartmann, Stefanie; Xenikoudakis, Georgios; Thomas, Jessica A.; Dehasque, Marianne; Sağlıcan, Ekin; Fidan, Fatma Rabia (17 February 2021). "Million-year-old DNA sheds light on the genomic history of mammoths". Nature. 591 (7849): 265–269. Bibcode:2021Natur.591..265V. doi:10.1038/s41586-021-03224-9. ISSN 1476-4687. PMC 7116897. PMID 33597750.
  21. ^ Ros-Montoya, Sergio; Palombo, Maria Rita; Espigares, María Patrocinio; Palmqvist, Paul; Martínez-Navarro, Bienvenido (October 2018). "The mammoth from the archaeo-paleontological site of Huéscar-1: A tile in the puzzling question of the replacement of Mammuthus meridionalis by Mammuthus trogontherii in the late Early Pleistocene of Europe". Quaternary Science Reviews. 197: 336–351. doi:10.1016/j.quascirev.2018.08.017.
  22. ^ Herridge, V. L.; Lister, A. M. (2012). "Extreme insular dwarfism evolved in a mammoth". Proceedings of the Royal Society B: Biological Sciences. 279 (1741): 3193–3300. doi:10.1098/rspb.2012.0671. PMC 3385739. PMID 22572206.
  23. ^ a b Haynes, Gary (March 2022). "Late Quaternary Proboscidean Sites in Africa and Eurasia with Possible or Probable Evidence for Hominin Involvement". Quaternary. 5 (1): 18. doi:10.3390/quat5010018. ISSN 2571-550X.
  24. ^ Tappen, Martha; Bukhsianidze, Maia; Ferring, Reid; Coil, Reed; Lordkipanidze, David (October 2022). "Life and death at Dmanisi, Georgia: Taphonomic signals from the fossil mammals". Journal of Human Evolution. 171: 103249. Bibcode:2022JHumE.17103249T. doi:10.1016/j.jhevol.2022.103249. PMID 36116366.
  25. ^ Yravedra, José; Courtenay, Lloyd A.; Gutiérrez-Rodríguez, Mario; Reinoso-Gordo, Juan Francisco; Saarinen, Juha; Égüez, Natalia; Luzón, Carmen; Rodríguez-Alba, Juan José; Solano, José A.; Titton, Stefania; Montilla-Jiménez, Eva; Cámara-Donoso, José; Herranz-Rodrigo, Darío; Estaca, Verónica; Serrano-Ramos, Alexia (April 2024). "Not seen before. Unveiling depositional context and Mammuthus meridionalis exploitation at Fuente Nueva 3 (Orce, southern Iberia) through taphonomy and microstratigraphy". Quaternary Science Reviews. 329: 108561. Bibcode:2024QSRv..32908561Y. doi:10.1016/j.quascirev.2024.108561. hdl:10261/355323.
  26. ^ Konidaris, George E.; Tourloukis, Vangelis (2021-04-14). "Proboscidea-Homo interactions in open-air localities during the Early and Middle Pleistocene of western Eurasia: a palaeontological and archaeolocigal perspective". Human-Elephant Interactions: From Past to Present. doi:10.15496/publikation-55599.

Bibliography

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Media related to Mammuthus meridionalis at Wikimedia Commons

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