Extinct members of Proboscidea include the deinotheres, mastodons, gomphotheres and stegodonts. The family Elephantidae also contains several extinct groups, including mammoths and Palaeoloxodon. Proboscideans include some of the largest known land mammals, with the elephant Palaeoloxodon namadicus and mastodon "Mammut" borsoni suggested to have body masses surpassing 16 tonnes (35,000 lb), rivalling or exceeding paraceratheres (the otherwise largest known land mammals) in size.[2] The largest extant proboscidean is the African bush elephant, with a world record of size of 4 m (13.1 ft) at the shoulder and 10.4 t (11.5 short tons).[2] In addition to their enormous size, later proboscideans are distinguished by tusks and long, muscular trunks, which were less developed or absent in early proboscideans.
Evolution
Over 180 extinct members of Proboscidea have been described.[3] The earliest proboscideans, Eritherium and Phosphatherium are known from the late Paleocene of Africa.[4] The Eocene included Numidotherium, Moeritherium and Barytherium from Africa. These animals were relatively small and some, like Moeritherium and Barytherium were probably amphibious.[5][6]
A major event in proboscidean evolution was the collision of Afro-Arabia with Eurasia, during the Early Miocene, around 18-19 million years ago allowing proboscideans to disperse from their African homeland across Eurasia, and later, around 16-15 million years ago into North America across the Bering Land Bridge. Proboscidean groups prominent during the Miocene include the deinotheres, along with the more advanced elephantimorphs, including mammutids (mastodons), gomphotheres, amebelodontids (which includes the "shovel tuskers" like Platybelodon), choerolophodontids and stegodontids.[7] Around 10 million years ago, the earliest members of the family Elephantidae emerged in Africa, having originated from gomphotheres.[8] The Late Miocene saw major climatic changes, which resulted in the decline and extinction of many proboscidean groups such as amebelodontids and choerolophodontids.[7] The earliest members of modern genera of Elephantidae appeared during the latest Miocene-early Pliocene around 6-5 million years ago. The elephantid genera Elephas (which includes the living Asian elephant) and Mammuthus (mammoths) migrated out of Africa during the late Pliocene, around 3.6 to 3.2 million years ago.[9]
Over the course of the Early Pleistocene, all non-elephantid probobscideans outside of the Americas became extinct (including mammutids, gomphotheres and deinotheres), with the exception of Stegodon.[7] Gomphotheres dispersed into South America during this era as part of the Great American interchange,[10] and mammoths migrating into North America around 1.5 million years ago.[11] At the end of the Early Pleistocene, around 800,000 years ago the elephantid genus Palaeoloxodon dispersed outside of Africa, becoming widely distributed in Eurasia.[12] By the beginning of the Late Pleistocene, proboscideans were represented by around 23 species. Proboscideans underwent a dramatic decline during the Late Pleistocene as part of the Late Pleistocene megafauna extinctions, with all remaining non-elephantid proboscideans (including Stegodon, mastodons, and the American gomphotheres Cuvieronius and Notiomastodon) and Palaeoloxodon becoming extinct, with mammoths only surviving in relict populations on islands around the Bering Strait into the Holocene, with their latest survival being on Wrangel Island around 4,000 years ago.[7][13]
The following cladogram is based on endocasts.[14]
Over the course of their evolution, proboscideans experienced a significant increase in body size. Some members of the families Deinotheriidae, Mammutidae, Stegodontidae and Elephantidae are thought to have exceeded modern elephants in size, with shoulder heights over 4 metres (13 ft) and masses over 10 tonnes (22,000 lb), with average fully grown males of the mammutid "Mammut" borsoni having an estimated body mass of 16 tonnes (35,000 lb), making it one the largest and perhaps the largest land mammal ever, with a fragmentary specimen of the Indian elephant species Palaeoloxodon namadicus only known from a partial femur being speculatively estimated in the same study to have possibly reached a body mass of 22 tonnes (49,000 lb).[15] As with other megaherbivores, including the extinct sauropod dinosaurs, the large size of proboscideans likely developed to allow them to survive on vegetation with low nutritional value.[16] Their limbs grew longer and the feet shorter and broader.[17] The feet were originally plantigrade and developed into a digitigrade stance with cushion pads and the sesamoid bone providing support, with this change developing around the common ancestor of Deinotheriidae and Elephantiformes.[18] Members of Elephantiformes which have retracted nasal regions of the skull indicating the development of a trunk, as well as well-developed tusks on the upper and lower jaws.[19]
The skull grew larger, especially the cranium, while the neck shortened to provide better support for the skull. The increase in size led to the development and elongation of the mobile trunk to provide reach. The number of premolars, incisors and canines decreased. The cheek teeth (molars and premolars) became larger and more specialised.[17] In Elephantiformes, the second upper incisor and lower incisor were transformed into ever growing tusks.[20][21] The tusks are proportionally heavy for their size, being primarily composed of dentine. In primitive proboscideans, a band of enamel covers part of the tusk surface, though in many later groups including modern elephants the band is lost, with elephants only having enamel on the tusk tips of juveniles. The upper tusks were initially modest in size, but from the Late Miocene onwards proboscideans developed increasingly large tusks, with the longest ever recorded tusk being 5.02 metres (16.5 ft) long belonging to the mammutid "Mammut" borsoni found in Greece, with some mammoth tusks likely weighing over 200 kilograms (440 lb). The lower tusks are generally smaller than the upper tusks, but could grow to large sizes in some species, like in Deinotherium (which lacks upper tusks), where they could grow over 1.5 metres (4.9 ft) long, the amebelodontidKonobelodon has lower tusks 1.61 metres (5.3 ft) long, with the longest lower tusks ever recorded being from the primitive elephantid Stegotetrabelodon which are around 2.2 metres (7.2 ft) long.[22]
The molar teeth changed from being replaced vertically as in other mammals to being replaced horizontally in the clade Elephantimorpha.[23] While early Elephantimorpha generally had lower jaws with an elongated mandibular symphysis at the front of the jaw with well developed lower tusks/incisors, from the Late Miocene onwards, many groups convergently developed brevirostrine (shortened) lower jaws with vestigial or no lower tusks.[24][25] Elephantids are distinguished from other proboscideans by a major shift in the molar morphology to parallel lophs rather than the cusps of earlier proboscideans, allowing them to become higher crowned (hypsodont) and more efficient in consuming grass.[26]
Several species of proboscideans lived on islands and experienced insular dwarfism. This occurred primarily during the Pleistocene, when some elephant populations became isolated by fluctuating sea levels, although dwarf elephants did exist earlier in the Pliocene. These elephants likely grew smaller on islands due to a lack of large or viable predator populations and limited resources. By contrast, small mammals such as rodents develop gigantism in these conditions. Dwarf proboscideans are known to have lived in Indonesia, the Channel Islands of California, and several islands of the Mediterranean.[27]
It has been suggested that members of Elephantimorpha, including mammutids,[30] gomphotheres,[31] and stegodontids,[32] lived in herds like modern elephants. Analysis of remains of the American mastodon (Mammut americanum) suggest that like modern elephants, that herds consisted of females and juveniles and that adult males lived solitarily or in small groups, and that adult males periodically engaged in fights with other males during periods similar to musth found in living elephants. These traits are suggested to be inherited from the last common ancestor of elephantimorphs,[30] with musth-like behaviour also suggested to have occurred in gomphotheres.[33] All elephantimorphs are suggested to have been capable of communication via infrasound, as found in living elephants.[34] Deinotheres may have also lived in herds, based on tracks found in the Late Miocene of Romania.[35] Over the course of the Neogene and Pleistocene, various members of Elephantida shifted from a browse-dominated diet towards mixed feeding or grazing.[36]
Classification
Below is a taxonomy of proboscidean genera as of 2019.[37][38][39][40]
^H. Saegusa, H. Nakaya, Y. Kunimatsu, M. Nakatsukasa, H. Tsujikawa, Y. Sawada, M. Saneyoshi, T. Sakai Earliest elephantid remains from the late Miocene locality, Nakali, Kenya Scientific Annals, School of Geology, Aristotle University of Thessaloniki, Greece VIth International Conference on Mammoths and Their Relatives, vol. 102, Grevena -Siatista, special volume (2014), p. 175
^Carpenter, K. (2006). "Biggest of the big: a critical re-evaluation of the mega-sauropod Amphicoelias fragillimus Cope, 1878". In Foster, J.R.; Lucas, S.G. (eds.). Paleontology and Geology of the Upper Jurassic Morrison Formation. New Mexico Museum of Natural History and Science Bulletin. Vol. 36. New Mexico Museum of Natural History and Science. pp. 131–138.
^Tikhonov, A.; Agenbroad, L.; Vartanyan, S. (2003). "Comparative analysis of the mammoth populations on Wrangel Island and the Channel Islands". Deinsea. 9: 415–20. ISSN0923-9308.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^Wang, Shi-Qi; Deng, Tao; Ye, Jie; He, Wen; Chen, Shan-Qin (2017). "Morphological and ecological diversity of Amebelodontidae (Proboscidea, Mammalia) revealed by a Miocene fossil accumulation of an upper-tuskless proboscidean". Journal of Systematic Palaeontology. 15 (8): 601–615. Bibcode:2017JSPal..15..601W. doi:10.1080/14772019.2016.1208687. S2CID89063787.