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Columbian mammoth

Extinct species of mammoth that inhabited North America

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Skeleton of Mammuthus columbi on display at the Page Museum at the La Brea Tar Pits.
Jonathan Chen · CC BY-SA 4.0

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Through Extinction, Species and Molar (tooth)

Reaching 3.72–4.2 m (12.2–13.8 ft) at the shoulders and 9.2–12.5 t (9.1–12.3 long tons; 10.1–13.8 short tons) in weight, the Columbian mammoth was one of the largest species of mammoth, larger than the woolly mammoth and the African bush elephant. It had long, curved tusks and four molars at a time, which were replaced six times during the lifetime of an individual. It most likely used its tusks and trunk like modern elephants—for manipulating objects, fighting, and foraging. Bones, hair, dung, and stomach contents have been discovered, but no preserved carcasses are known. The Columbian mammoth preferred open areas, such as parkland landscapes, and fed on sedges, grasses, and other plants. It did not live in the Arctic regions of Canada, which were instead inhabited by woolly mammoths. The ranges of the two species may have overlapped, and genetic evidence suggests that they interbred. Several sites contain the skeletons of multiple Columbian mammoths, either because they died in incidents such as a drought, or because these locations were natural traps in which individuals accumulated over time.

For a few thousand years prior to their extinction, Columbian mammoths coexisted in North America with Paleoindians – the first humans to inhabit the Americas – who hunted them for food, used their bones for making tools, and possibly depicted them in ancient art. Columbian mammoth remains have been found in association with Clovis culture artifacts. The Clovis peoples are suggested to have been specialized mammoth hunters, though they possibly also scavenged their remains. The last Columbian mammoths are dated to about ~12,000 years ago, with the species becoming extinct as part of the Late Pleistocene extinction event, simultaneously with most other large megafaunal mammals present in the Americas. It is one of the last recorded North American megafauna to have gone extinct. The extinction of the Columbian mammoth and other American megafauna was most likely a result of habitat loss caused by climate change, hunting by humans, or a combination of both.

Taxonomy

Around 1725, enslaved Africans digging in the vicinity of the Stono River in South Carolina unearthed 3-4 molar teeth now known to have belonged to Columbian mammoths, which were subsequently examined by the British naturalist Mark Catesby, who visited the site, and published his account of the visit in 1743. While the slave owners were puzzled by the objects and suggested that they originated from the great flood described in the Bible, Catesby noted that the slaves unanimously agreed that the objects were in fact the teeth of elephants, similar to those of African elephants that they were familiar with from their homeland, to which Catesby concurred, marking the first technical identification of any fossil animal in North America. A similar observation was made in 1782 after enslaved Africans had excavated mammoth bones and teeth from a salt marsh in Virginia. These remains were subsequently sent on by US army commander Arthur Campbell to future US president Thomas Jefferson. Campbell noted in a letter that several Africans had seen one of the teeth, and "All ... pronounced it an elephant." Catesby's account was later noted by the French paleontologist Georges Cuvier around the beginning of the 19th century, with Cuvier personally examining the teeth from Stono, which he used to support his theory of catastrophism.

The Columbian mammoth was first scientifically described in 1857 by the Scottish naturalist Hugh Falconer, who named the species Elephas columbi after the explorer Christopher Columbus. The animal was brought to Falconer's attention in 1846 by the Scottish geologist Charles Lyell, who sent him molar fragments found during the 1838 excavation of the Brunswick–Altamaha Canal in Georgia, in the southeastern United States. At the time, similar fossils from across North America were attributed to woolly mammoths (then Elephas primigenius). Falconer found that his specimens were distinct, confirming his conclusion by examining their internal structure and studying additional molars from Mexico. Although scientists William Phipps Blake and Richard Owen believed that E. texianus was more appropriate for the species, Falconer rejected the name; he also suggested that E. imperator and E. jacksoni, two other American elephants described from molars, were based on remains too fragmentary to classify properly. More complete material that may be from the same quarry as Falconer's fragmentary holotype molar (which is cataloged as specimen BMNH 40769 at the British Museum of Natural History) was reported in 2012, and could help shed more light on that specimen, since doubts about its adequacy as a holotype have been raised.

In the early 20th century, the taxonomy of extinct elephants became increasingly complicated. In 1942, the American paleontologist Henry Fairfield Osborn's posthumous monograph on the Proboscidea was published, wherein he used various generic and subgeneric names that had previously been proposed for extinct elephant species, such as Archidiskodon, Metarchidiskodon, Parelephas, and Mammonteus. Osborn also retained names for many regional and intermediate subspecies or "varieties", and created recombinations such as Parelephas columbi felicis and Archidiskodon imperator maibeni.

The taxonomic situation was simplified by various researchers from the 1970s onwards; all species of mammoth were retained in the genus Mammuthus, and many proposed differences between species were instead interpreted as intraspecific variation. In 2003, the American paleontologist Larry Agenbroad reviewed opinions about North American mammoth taxonomy, and concluded that several species had been declared junior synonyms, and that M. columbi (the Columbian mammoth) and M. exilis (the pygmy mammoth) were the only species of mammoth endemic to the Americas (as other species lived both there and in Eurasia). The idea that species such as M. imperator (the imperial mammoth) and M. jeffersoni (Jefferson's mammoth) were either more primitive or advanced stages in Columbian mammoth evolution was largely dismissed, and they were regarded as synonyms. In spite of these conclusions, Agenbroad cautioned that American mammoth taxonomy is not yet fully resolved.

Evolution

The earliest known members of Proboscidea, the clade that contains the elephants, existed about 55 million years ago around the Tethys Sea area. The closest living relatives of the Proboscidea are the sirenians (dugongs and manatees) and the hyraxes (an order of small, herbivorous mammals). The family Elephantidae existed six million years ago in Africa, and includes the living elephants and the mammoths. Among many now extinct clades, the mastodon (Mammut) is only a distant relative, and part of the distinct family Mammutidae, which diverged 25 million years before the mammoths evolved. The Asian elephant (Elephas maximus) is the closest extant relative of the mammoths. The following cladogram shows the placement of the Columbian mammoth among other Late Pleistocene proboscideans, based on genetic studies:

Since many remains of each species of mammoth are known from several localities, reconstructing the evolutionary history of the genus is possible 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 taller in height and the skulls became taller to accommodate this. At the same time, the skulls became shorter from front to back to reduce the weight of the head. The short, tall skulls of woolly and Columbian mammoths are the culmination of this process.

The first known members of the genus Mammuthus are the African species M. subplanifrons from the Pliocene, and M. africanavus from the Pleistocene. The former is thought to be the ancestor of later forms. Mammoths entered Europe around 3 million years ago. The earliest European mammoth has been named M. rumanus; it spread across Europe and China. Only its molars are known, which show that it had 8–10 enamel ridges. A population evolved 12–14 ridges, splitting off from and replacing the earlier type, becoming M. meridionalis about 2.0–1.7 million years ago. In turn, this species was replaced by the steppe mammoth (M. trogontherii) with 18–20 ridges, which evolved in eastern Asia around 2.0–1.5 million years ago. The Columbian mammoth evolved from a population of M. trogontherii that had crossed the Bering Strait and entered North America about 1.5-1.3 million years ago; it retained a similar number of molar ridges. Mammoths derived from M. trogontherii evolved molars with 26 ridges 400,000 years ago in Siberia and became the woolly mammoth (M. primigenius). Woolly mammoths entered North America about 100,000 years ago.

A population of mammoths derived from Columbian mammoths that lived between 80,000 and 13,000 years ago on the Channel Islands of California, 10 km (6.2 mi) away from the mainland, evolved to be less than half the size of the mainland Columbian mammoths. They are, therefore, considered to be the distinct species M. exilis, the pygmy mammoth (or a subspecies, M. c. exilis). These mammoths presumably reached the islands by swimming there when sea levels were lower, and decreased in size due to the limited food provided by the islands' small areas. Bones of larger specimens have also been found on the islands, but whether these were stages in the dwarfing process, or later arrivals of Columbian mammoths is unknown.

Hybridization

A 2011 ancient DNA study of the complete mitochondrial genome (inherited through the female line) showed that two examined Columbian mammoths, including the morphologically typical "Huntington mammoth", were grouped within a subclade of woolly mammoths. This suggests that the two populations interbred and produced fertile offspring. One possible explanation is introgression of a haplogroup from woolly to Columbian mammoths, or vice versa. A similar situation has been documented in modern species of African elephant (Loxodonta), the African bush elephant (L. africana) and the African forest elephant (L. cyclotis). The authors of the study also suggest that the North American type formerly referred to as M. jeffersonii may have been a hybrid between the two species, as it is apparently morphologically intermediate. These findings were unexpected, and other researchers requested further study to clarify the situation.

A 2015 study of mammoth molars confirmed that M. columbi evolved from Eurasian M. trogontherii, not M. meridionalis as had been suggested earlier, and noted that M. columbi and M. trogontherii were so similar in morphology that their classification as separate species may be questionable. The study also suggested that the animals in the range where M. columbi and M. primigenius overlapped formed a metapopulation of hybrids with varying morphology. In 2016, a genetic study of North American mammoth specimens confirmed that the mitochondrial diversity of M. columbi was nested within that of M. primigenius and suggested that both species interbred extensively, were both descended from M. trogontherii, and concluded that morphological differences between fossils may, therefore, not be reliable for determining taxonomy. The authors also questioned whether M. columbi and M. primigenius should be considered "good species", considering that they were able to interbreed after supposedly being separated for a million years, but cautioned that more specimens need to be sampled.

In 2021, DNA older than a million years was sequenced for the first time, from two steppe mammoth-like teeth of Early Pleistocene age found in eastern Siberia. One tooth from Adyocha (1-1.3 million years old) belonged to a lineage that was ancestral to later woolly mammoths, whereas the other from Krestovka (1.1–1.65 million years old) belonged to new lineage, possibly a distinct species, that is estimated to have split from the ancestors of woolly mammoths around 2.7-1.8 million years ago. The study found that a large proportion of the ancestry of Columbian mammoths came from the Krestovka lineage, which were probably representative of the first mammoths to have colonized North America, and another substantial contribution coming from early representatives of the woolly mammoth lineage, with the hybridisation between the two lineages likely happening at least 420,000 years ago, during the Middle Pleistocene, resulting in the Columbian mammoths of the Late Pleistocene having around 40-50% ancestry from the Krestovka lineage, and 50-60% related to woolly mammoths. Later woolly and Columbian mammoths also interbred occasionally, and mammoth species perhaps hybridized routinely when brought together by glacial expansion. The study also found that genetic adaptations to cold environments, such as hair growth and fat deposits, were already present in the steppe mammoth lineage, and was not unique to woolly mammoths. This research has raised questions about which material the name Mammuthus columbi should be applied to, as there is no obvious difference in tooth morphology between Early Pleistocene presumably pre-hybridisation North American mammoths and later Pleistocene M. columbi. In a 2024 review, Adrian Lister and Love Dalén argued that M. columbi should be retained in a broad sense covering the entire time-period of mammoth occupation of North America.

A 2025 study found that two genetically sequenced molar teeth of Late Pleistocene age in British Columbia, Canada, belonged to mammoths of predominantly woolly mammoth ancestry, but harbored significant levels (21.6 ± 0.9% and 34.6 ± 0.1%) of Columbian mammoth ancestry, indicating interbreeding and bidirectional gene flow between Columbian mammoths and woolly mammoths during the Late Pleistocene in North America where their ranges overlapped, rather than just undirectional woolly mammoth gene flow into Columbian mammoths as had previously been recognized. Another 2025 study examining M. columbi from the Valley of Mexico doubled the number of known mitochondrial genomes, and revealed that Mexican M. columbi possessed a highly divergent mitochondrial lineage (with diverse sub-lineages), which was separate to the mitochondrial lineages present in both woolly and Columbian mammoths in northern America. The last common ancestor between Mexican and northern American mammoths was 361,000 years ago (shortly after diverging from Eurasian woolly mammoths), while the divergence date between Columbian and woolly mammoths in northern America was 247,000 years ago.

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