Jump to content

Arctodus

From Wikipedia, the free encyclopedia
(Redirected from A. simus)

Arctodus
Temporal range: Pleistocene
A. simus from the La Brea Tar Pits
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Family: Ursidae
Subfamily: Tremarctinae
Genus: Arctodus
Leidy, 1854
Type species
Arctodus pristinus
Leidy, 1854
Other species
  • A. simus (Cope, 1879)
Arctodus simus range
Synonyms
synonyms of A. pristinus
synonyms of A. simus
  • Arctodus nebrascensis Berger 1930
  • Arctotherium californicum Merriam 1911
  • Arctotherium simum Cope 1879
  • Arctotherium yukonense Lambe 1911
  • Dinarctotherium merriami Barbour 1916
  • Tremarctotherium simum Gidley 1928

Arctodus is an extinct genus of short-faced bear that inhabited North America during the Pleistocene (~2.5 Mya until 12,800 years ago). There are two recognized species: the lesser short-faced bear (Arctodus pristinus) and the giant short-faced bear (Arctodus simus). Of these species, A. simus was larger, is known from more complete remains, and is considered one of the best known members of North America's extinct Ice Age megafauna. A. pristinus was largely restricted to the Early Pleistocene of the eastern United States, whereas A. simus had a broader range, with most finds being from the Late Pleistocene of the United States, Mexico and Canada. A. simus evolved from A. pristinus, but both species likely overlapped in the Middle Pleistocene. Both species are relatively rare in the fossil record.

Today considered to be an enormous omnivore, Arctodus simus is believed to be one of the largest known terrestrial carnivorans that has ever existed. However, Arctodus, like other bears, was highly sexually dimorphic. Adult A. simus ranged between 300 and 950 kilograms (660 and 2,090 lb), with females clustering at ≤500 kilograms (1,100 lb), and males around 800 kilograms (1,800 lb). The largest males stood at 1.67 metres (5 ft 6 in) at the shoulder, and up to 3.4 metres (11 ft) tall on their rear legs. Studies suggest that Arctodus simus browsed on C3 vegetation and consumed browsing herbivores such as deer, camelids, and tapir. A. simus preferred temperate open woodlands but was an adaptable species, taking advantage of many habitats and feeding opportunities.

Arctodus belongs to the Tremarctinae subfamily of bears, which are endemic to the Americas. Of these short-faced bears, Arctodus was the most widespread in North America. However, the genus was restricted to the Pleistocene. A. pristinus went extinct around 300,000 years ago, with A. simus disappearing ~12,800 years ago in the Late Pleistocene extinctions. The cause behind these extinctions is unclear, but in the case of A. pristinus, this was likely due to climate change and competition with other ursids, such as the black bear and Tremarctos floridanus. A. simus likely went extinct due to ecological collapse disrupting the vegetation and prey it relied on.

Taxonomy

[edit]
Partial mandible of A. pristinus uncovered from Port Kennedy Cave.

Arctodus was first described by Joseph Leidy in 1854, with finds of A. pristinus from the Ashley Phosphate Beds, South Carolina.[1][2][3] The scientific name of the genus, Arctodus, derives from Greek, and means "bear tooth". The first fossils of Arctodus simus were found in the Potter Creek Cave, Shasta County, California, by J. A. Richardson in 1878, and were initially described as Arctotherium simum by Edward Drinker Cope in 1879.[4][5][6] Historically, all specimens were grouped together under A. pristinus, until a revision by Björn Kurtén in 1967.[7]

In the 19th and early 20th centuries, specimens of Arctodus were occasionally referred to Arctotherium, and vice versa.[6][8][9][10][11] However, today neither genera are considered to have overlapped, with the closest point of contact being México, with the giant Arctodus simus in Valsequillo, Puebla,[7][12][13] and the smaller Arctotherium wingei in the Yucatán Peninsula.[14] Other early researchers believed Arctodus to be a sister lineage of the agriotheriin Indarctos.[15] Sometimes described as the "American cave bear",[4][16] Arctodus should not be mistaken for the similarly large Eurasian cave bear (Ursus spelaeus). As an ursine, the Eurasian cave bear last shared a common ancestor with the tremarctine Arctodus circa 13.4 million years ago.[17]

Fossils of Arctodus pristinus can be confused with the similarly sized, partially contemporaneous short-faced bear, Tremarctos floridanus.[1] Arctodus has higher crowned and considerably larger teeth than its relative Tremarctos. A. pristinus can be distinguished by broader and taller molars on average, but as they are often worn, differentiation can be difficult.[2] Moreover, diagnosing isolated A. simus remains (such as femora, scapulae, certain vertebrae, ribs, podials) from brown bears can be challenging, as some large brown bears overlap in dimensions with small Arctodus simus.[7] Beyond standard differences between tremarctine and ursine bears, A. simus has a more anterior protocone & extended enamel ridge forming a shearing blade on the maxillary P4. The molars are also shorter & broader in Arctodus than brown bears.[18]

Evolution

[edit]
Tremarctinae within Ursidae

Hemicyoninae

Ursavinae

Ailuropodinae

Ursinae

Tremarctinae (short-faced bears)

Plionarctos

Arctodus

Arctodus belongs to the subfamily Tremarctinae, which appeared in North America during the earliest parts of the late Miocene epoch in the form of Plionarctos. The medium-sized Arctodus pristinus, Tremarctos floridanus and Arctotherium sp. evolved from Plionarctos in the Blancan age of North America.[2][19][20] The genetic divergence date for Arctodus is ~5 million years ago,[17][21] around the Miocene-Pliocene boundary, when tremarctine bears, along with other ursids, experienced an explosive radiation in diversity, as C4 vegetation (grasses) and open habitats dominated. The world experienced a major temperature drop and increased seasonality, and a faunal turnover which extinguished 70–80% of North American genera.[22][23]

Arctodus pristinus was mostly restricted to the more densely forested thermal enclave in eastern North America.[24][25] A. pristinus has the greatest concentration of fossils in Florida,[2] with the earliest finds being from the Late Blancan Kissimmee River 6 (2.7 - 2.2 Mya) and Santa Fe River 1 sites.[1][2][26] During the early Irvingtonian faunal stage, a western population of A. pristinus evolved into the enormous A. simus, with the earliest confirmed records being at least 780,000 years old from the Irvington type locality in California.[7][27] Correspondingly, A. simus is most plentiful from western North America,[28][29] albeit preferring mixed habitat such as temperate open woodlands.[30][31][32][33][34] Their ranges may have met in the Middle Pleistocene of Kansas,[7] with A. simus migrating east in the Late Pleistocene (around the extinction of A. pristinus).[20][35] Although both Arctodus species co-inhabited North America for at least half a million years during the Middle Pleistocene (A. pristinus went extinct ~300,000 BP), there is no direct evidence of overlap or competition in the fossil record as of yet, as both species established largely separate ranges.[20]

Irvingtonian age (1,900,000 BP - 250,000 BP) specimens of Arctodus simus are particularly sparse. Finds are mostly from California, with additional remains from Texas, Kansas, Nebraska, and Montana.[36][37][38] However, A. simus became a pan-continental species in the Rancholabrean faunal stage (Late Pleistocene), sharing that distinction with the black bear.[27][33] Despite Arctodus simus' large temporal and geographic range, fossil remains are comparatively rare (109 finds as of 2010, in otherwise well-sampled localities).[20][17]

Description

[edit]

Size

[edit]
Restoration of Arctodus simus.

Arctodus pristinus

[edit]

Around the size of grizzly bears, A. pristinus specimens closely overlap the size of Tremarctos floridanus, with some males of A. pristinus overlapping in size with the females of A. simus.[1] Floridan A. pristinus individuals were calculated to an average of ~140 kilograms (310 lb).[39][40] However, the dimensions of some individuals from Port Kennedy Bone Cave and Aguascalientes suggest that northern and western A. pristinus may have been larger than Floridan A. pristinus,[7] being up to 400 kilograms (880 lb).[41]

Arctodus simus

[edit]

Some A. simus individuals might have been the largest land-dwelling specimens of Carnivora that ever lived in North America. Standing up on its hind legs, A. simus stood 2.4–3.4 m (8–11 ft),[42][43] with a maximum vertical arm reach of 4.3 metres (14 ft).[44] When walking on all fours, A. simus stood 1–1.67 m (3.3–5.5 ft) high at the shoulder, with the largest males being tall enough to look an adult human in the eye.[45][43][46] The average weight of A. simus was ~625 kilograms (1,378 lb), with the maximum recorded at 957 kilograms (2,110 lb).[47][39]

Studies
[edit]

In a 2010 study, the mass of six A. simus specimens was estimated; half of the specimens weighed between 740 kg (1,631 lb) and 957 kg (2,110 lb), with a mean weight of ~850 kg, suggesting larger specimens were probably more common than previously thought. However, the other specimens were calculated to be less than 500 kg (1,100 lb). The weight range calculated from all examined specimens was between 957 kg and 317 kg (699 lb).[47] Hypothetically, the largest individuals of A. simus may have approached 1,000 kilograms (2,200 lb),[48] or even 1,200 kg (2,600 lb).[41] However, a 2006 study argued that the maximum size of Arctodus was ~555 kilograms (1,224 lb), based on the largest known skull.[49] Additionally, a 1998 study calculated the average weight of Arctodus specimens from the La Brea Tar Pits at ~372 kilograms (820 lb), smaller than recovered brown bear remains (~455 kilograms (1,003 lb), although these remains postdate Arctodus).[50][51][52] A 1999 study by Per Christiansen calculated a mean weight of ~770 kilograms (1,700 lb) from seven male A. simus limb bones, suggesting large males weighed between 700 kilograms (1,500 lb) and 800 kilograms (1,800 lb).[48]

Sexual dimorphism

[edit]
Arctodus simus skeletal at the Field Museum of Natural History, Chicago.

There is much variation in adult size among specimens- the lack of finds, sexual dimorphism, individual variation and potentially ecomorphs could be augmenting the average size of both species of Arctodus.[2][7][53] Size differences between specimens of Arctodus simus (such as skull and long bone dimensions) led Kurtén to suggest a larger northern/central subspecies (A. s. yukonensis) and a southern subspecies (A. s. simus).[47][7][38] evolving in the Irvingtonian and Rancholabrean respectively.[38][7] However, the discovery of a very large southern Arctodus simus in Florida and New Mexico (deep within the supposed range of A. s. simus),[20][54] & possibly Rancho La Brea,[7][36] and notably small specimens from the Yukon and Vancouver Island,[17][18] put doubt on this designation.[55] Perceived ecomorphologies are possibly due to the low number of specimens, and sex-biased sampling.[20]

For example, only one baculum (penis bone) has been recovered from over 100 giant short-faced bear sites in North America, although it may belong to a black bear (Potter Cave).[56] None of the specimens assigned to the larger morph (A. s. yukonensis) is from a cave passage, being usually isolated remains from open sites. Furthermore, over 70% of the smaller specimens (once assigned as the A. s. simus subspecies) are from cave deposits where bacula would likely be found if present, suggesting that mostly female individuals of A. simus were using caves.[57][40][7] Therefore, in conjunction with ursid sexual dimorphism (e.g. male spectacled bears are 30% - 40% larger than females), the larger, massive Arctodus individuals are often considered male, particularly older males, with the smaller, more lightly built individuals being females.[20][58][36] Sexual dimorphism may also explain A. simus teeth (from multiple individuals at the same site) generally clustering into two sizes.[7]

Anatomy

[edit]

The two species of Arctodus are differentiated not only by size, but also by the shorter snout, greater prognathism, more robust teeth and longer limbs of A. simus, and the relative proportions of each species' molars and premolars. Arctodus pristinus is distinguished from A. simus smaller, narrower, and less crowded teeth. However, the morphologies of both species are otherwise very similar. As a result, differentiating Arctodus simus from Arctodus pristinus can be difficult, as male individuals of Arctodus pristinus can overlap in size with female individuals of Arctodus simus.[20][57][59] Arctodus simus superficially resembled living hyaenids in skull shape and relative lengths of the trunk, back and limbs.[49] The most nearly complete skeleton of A. simus found in the United States was unearthed in Fulton County, Indiana; the original bones are in the Field Museum of Natural History, Chicago.[45][56]

Skull

[edit]
Male A. simus skull, photographed at the Cleveland Museum of Natural History in Cleveland, Ohio.

Members of the Tremarctinae subfamily of bears appear to have a disproportionately short snout compared with most modern bears, giving them the name "short-faced". Arctodus has also been argued to exhibit a wide and shortened rostrum, potentially giving Arctodus a more felid-like appearance.[38][60] Matheus suggested that a broad snout could have housed a highly developed olfactory apparatus, or accommodated a larger throat passage to bolt down large food items, akin to spotted hyenas.[61] However, this apparent shortness is an illusion caused by the deep snouts and short nasal bones of tremarctine bears compared with ursine bears; Arctodus has a deeper but not a shorter face than most living bears. This characteristic is also shared by the only living tremarctine bear, the omni-herbivorous spectacled bear.[28][47][62] Snout deepness could be variable, as specimens from Huntington Reservoir in Utah, and the Hill-Shuler locality, Texas, were noted as being distinctly "short-faced" in comparison with other Arctodus simus individuals.[63][64]

The orbits of Arctodus are proportionally small compared to the size of the skull, and somewhat laterally orientated (a characteristic of tremarctine bears), more so than actively predatory carnivorans or even the brown bear, suggesting that stereoscopic vision was not a priority.[49][62][65] The optic canal and other sphenoidal openings crowd together more in A. simus than in Ursus.[18] As with Tremarctos ornatus, specimens with a large sagittal crest were likely male, whereas females had a reduced or no sagittal crest.[2] Although there are limited samples, the middle ear bones of A. simus are proportionally larger than modern ursine bears, suggesting the species was particularly attuned to low-frequency sounds.[66]

Morphologically, Arctodus simus exhibits masticular characteristics common to herbivorous bears. This includes cheek teeth with large, blunt surface areas, a deep mandible, and large mandibular muscle attachments (which are rare in carnivorous mammals). As herbivorous carnivorans such as Arctodus lack the gut microbiota to efficiently break down plant matter, these features created a high mechanical advantage of the jaw to break down plant matter via extensive chewing or grinding.[28][23][67] Although the low mandibular condyle relative to the tooth row (and therefore potential wide gape) of Arctodus simus has been inferred as an adaptation for carnivory,[38][68][18] it is also present in the omni-herbivorous spectacled bear.[47] However, both Arctodus pristinus and Tremarctos floridanus have condyles raised well above the plane of the teeth.[69] The purpose of the highly vaulted calvarium and straight cheek bones of Arctodus simus have been similarly disputed.[47]

A 2009 analysis of the mandibular morphology of tremarctine bears found notable differences between Arctodus pristinus and Arctodus simus, with A. simus specimens possessing a concave jaw, large masseter and temporalis muscles, deeper horizontal ramus and a reduced slicing dentition length when compared to A. pristinus. Instead, Arctodus simus was most similar to Arctotherium angustidens- however, both species of Arctodus and Arctotherium angustidens were still comfortably in the "omnivorous" bear cranio-morphotype.[62]

Dentition
[edit]
Right lower second molar (M2) of Arctodus simus, from Rancho La Brea, California.

The premolars and first molars of Arctodus pristinus are relatively smaller and more widely spaced than those of Arctodus simus.[1][20] In A. pristinus, the features of the dentition can be quite variable, particularly the M2 molar.[2] An analysis of the Hunter-Schreger bands from the teeth of A. pristinus and A. simus demonstrated an evolutionary trend towards partially reinforced tooth enamel. This has been convergently evolved with giant pandas, agriotheriin bears, and Hemicyon.[70] The dentition of A. simus has been used as evidence of a predatory lifestyle- in particular the large canines, the high-crowned lower first molar, and the possible carnassial shear with the upper fourth premolar. However, the wearing of the molars to a relatively flat & blunt loph (suitable as a crushing platform as per modern omnivorous bears), small shear facet, and the flattened cusps across age ranges (unlike carnivores, which instead have carnassial shears) disagrees with this hypothesis.[28][71][18]

Dentition can be a poor indicator of size in A. simus, as some medium-size individuals have teeth that surpass the size of those with the largest skeletons.[7] Additionally, while A. simus evolved from the smaller A. pristinus, their teeth remained generally the same size.[7] A specimen of A. simus from the Seale Pit of the Hill-Shuler locality, Texas, with only two premolars, crowding of the anterior premolar out of line, and a wider and shorter muzzle, was suggested to be an undescribed form of Arctodus.[64]

Post-cranial

[edit]
Limbs
[edit]
A. simus compared with a human.

Researchers have differing interpretations on the limb morphology of Arctodus. A comprehensive 2010 study concluded that the legs of Arctodus weren't proportionally longer than modern bears would be expected to have, and that bears in general are long-limbed animals, obscured in life by their girth and fur. The study concluded the supposed "long-legged" appearance of the bear is largely an illusion created by the animal's relatively shorter back and torso. In fact, Arctodus probably had an even shorter back than other bears, due the necessary ratio between body length and body mass of the huge bear.[47][72] However, other researchers argue that the limb bones of Arctodus simus are proportionally longer than those of other bears, leading to a "gracile" appearance. Although longer, the proportions still overlap with Ursus, and the limb bones are stouter than in the large-bodied felids (Panthera). Rather than for running, these elongated limb bones may have evolved for increased locomotor efficiency during prolonged travel.[73][74] This stiff-legged, swinging gait could have been similar to a polar bear's.[75] Some researchers suggest that proportionally longer limbs may be an adaptation for increased vision over tall ground cover in an open habitat, or were used in tearing and pulling down vegetation.[28][46]

Researchers also disagree when interpreting the humerus of Arctodus simus.[73] Sorkin argued that the pronation of the forearm and the flexion of the wrist and digits, and more lightly muscled forelimbs, all of which are crucial to grasping a large prey animal with the forepaws, were probably less powerful in Arctodus than in either the brown bear or in Panthera. This is due to a weak medial epicondyle and reduced development of the pronator teres muscle.[49] The forelimb of Arctodus could have been in the early stages of cursorial evolution, being capable of more efficient and high-speed straight-line locomotion (relative to extant bears), and was possibly more adept at pursuing large prey than polar and brown bears.[76] On the other hand, some researchers argue that the epicondyles were still well developed, with this wide range of ulna rotation suggests that forearms of Arctodus were powerful and could subdue large prey.[73] A 2013 examination of Rancho La Brean specimens found that they did not possess distally elongated limbs, which discredited cursoriality. Furthermore, the relatively broad humeral & femoral epicondyles were characteristic of diggers and polar bears, and suggested Arctodus simus could have foraged for roots, tubers and ground squirrels and/or had developed forelimb muscles to immobilze moving prey.[77] The shape of the elbow joint, along with an well-developed medial epicondyle which forms an angle with the condyle, and shallower olecranon fossa, would have given Arctodus a higher degree of forelimb dexterity. Originally evolved to facilitate arboreality, other researchers believe that the terrestrial Arctodus (along with Arctotherium and the giant panda) retained this characteristic to assist in foraging for vegetation.[21][28][78]

Paws
[edit]

The paws (metapodials and phalanges) of Arctodus were characteristically long, slender, and more elongated along the third and fourth digits compared to ursine bears. Arctodus' paws were therefore more symmetrical than ursine bears, whose feet have axes aligned with the most lateral (fifth) digit. Also, the first digit of Arctodus was positioned more closely and parallel to the other four digits (i.e. with straight toes, Arctodus had less lateral splaying).[72][46]

For comparison, the manus of the spectacled bear has five digits arrayed in a shallow arc (Chaquil Cave, Peru).[79][80]

However this is potentially contradicted by possible Arctodus simus trackways from near Lakeview, Oregon, with strong toe splaying, three centrally aligned & evenly spaced toes at the front, and two almost perpendicular lateral toes (80° from the axis of the foot on either side). The trackways suggest that Arctodus had an oval-shaped, undivided pad on its sole, front paws that were slightly larger than its back paws, possessed long claws, and had its hind foot overstep the forefoot when walking, like modern bears.[81] An additional A. simus paw print measuring 15 cm (5.9 in) long and 19 cm (7.5 in) wide has been recovered from White Sands National Park, New Mexico.[82][83] Some claw marks attributed to Arctodus simus at Riverbluff Cave (as they were four meters above the floor of the cave) were nearly 20 cm in width.[84][85]

The presence of a partial false thumb in Arctodus simus is a characteristic shared with Tremarctos floridanus and the spectacled bear, and is possibly an ancestral trait. Absent in ursine bears, the false thumb of the spectacled bear has been suggested to assist in herbivorous food manipulation (such as bromeliads, leaves, berries, tree bark & fruits, cactus fruits & pulp, palm hearts & fronds), or arboreality.[86][23][28]

Paleopathology

[edit]

Beyond carbohydrate-associated dental pathologies present in the genus,[57][87][18] extensive pathologies have been preserved on the most nearly complete skeleton of Arctodus. The leading hypothesis suggests the Fulton County Arctodus specimen suffered from a syphilis-like (treponemal) disease, or yaws, based on the various lesions present.[45][88][89] The same individual records a pathological growth distorting the right humerus,[49] with abscesses are noted between the molars and on both ulna. Hypotheses include syphilis, osteoarthritis, a fungal infection in addition to long term syphilis, or an infected wound.[45][90] Several specimens from Fairbanks, Alaska, also exhibit either pathological growths or periodontal disease,[7] along with a healed toe bone from Big Bear Cave, Missouri.[56]

Paleobiology

[edit]

Locomotion

[edit]

Paul Matheus proposed that Arctodus simus may have moved in a highly efficient, moderate-speed pacing gait, more specialized than modern bears. His research concluded that the large body size, taller front legs, high shoulders, short and sloping back, and long legs of Arctodus also compounded locomotive efficiency, as these traits swelled the amount of usable elastic strain energy in the tendons, and increased stride length, making Arctodus built more for endurance than for great speed.[42][74] His calculations suggested that Arctodus likely had a top speed of 40–45 kilometres per hour (25–28 mph), and based on hyaenid proportions, would shift from singlefoot locomotion to a pace at 8.5 km/h (5.3 mph), and would begin to gallop at 18.5 km/h (11.5 mph), a fairly high speed. Based on other mammals, the optimal pace speed of Arctodus would have been 13.7 km/h (8.5 mph). For comparison, hyenas cross country ~10 km/h (6.2 mph).[74] This mobility would have facilitated travelling across a large home range, which Mattson suggests may have topped 1,000 square miles (2,600 km2).[56] Swimming has also been presented as a hypothesis for the colonization of Vancouver Island by Arctodus simus.[91][56]

Maturity

[edit]

Examinations on a mostly full sized young individual of Arctodus simus from an Ozark cave suggest that Arctodus, like other ursids, reached sexual maturity well before full maturity. Comparisons with black bears suggest the Arctodus specimen was either 4–6 years of age if female, or 6–8 years if the specimen was male. Additionally, wear patterns on the individual's teeth are similar to a 4-6 year old Ursus americanus. Fused sutures, epiphyses, and epiphyseal plates, along with tooth eruption, have been used to determine adulthood in Arctodus.[57][17]

Genetic diversity

[edit]
Arctodus is located in North America
Chiquihuite Cave
Sheriden Cave (E)
Natural Trap Cave (N/A)
San Miguel Island (N/A)
Clover Bar (Edmonton, F)
Cripple Creek (F)
Sixtymile River (F)
Dawson (Canyon Creek, Dawson City, Eldorado Creek, Gold Run, Hester Creek, Lower Hunker Creek, Ophir Creek, Quartz Creek, ADF)
Lilian Creek (A)
Fairbanks (Dawson Cut, Ester Creek, Eva Creek Mine, Gold Hill, Goldstream, No.2 G-Strip Area, ABCDFG)
DNA distribution map of Arctodus simus

Legend: Main mitochondrial haplogroup of A. simus (haplotypes A, B, C, D, E, F, G)

Chiquihuite Cave A.simus

Unassigned A.simus

An examination of mitochondrial DNA sequenced from specimens of Arctodus simus from Alaska, Alberta, Ohio and the Yukon suggest an extremely low level of genetic diversity among the 23 individuals studied (≤ 44,000 14C BP), with only seven haplotypes recovered. Genetic diversity was comparable to modern endangered fauna, such as the brown kiwi and African cheetah. Explanations include a genetic bottleneck before 44,000 14C BP, or a low level of genetic diversity being a feature of a species which was primarily solitary, with a large home range and relatively small population size.[92] However, this does not entirely preclude genetic diversity in Arctodus simus, with genetic samples from Chiquihuite Cave, Zacatecas indicating a deep divergence with previously studied specimens of A. simus.[17] Additional specimens from the California Channel Islands and Wyoming have been sequenced, but are unassigned.[93]

Haplotype cladogram

[edit]

Below is a cladogram exploring the relationships between the mitochondrial haplogroups of Arctodus simus. Other than the specimen from Chiquihuite Cave, all haplotypes form a single clade.[17][92]

Chiquihuite Cave

A

B

C

D

E

F

G

Diet

[edit]

Herbivory

[edit]
Arctodus faeces found at South Dakota and the Yukon contain Juniperus seeds. Seed cones and berries are still important food sources for northern bears today.

The fact that Arctodus did not significantly differ in dentition or build from modern bears has led most authors to support the hypothesis that the A. simus was omnivorous, like most modern bears, and would have eaten significant amounts of plant matter.[71][94] Morphologically, Arctodus simus exhibits masticular and dental characteristics which confirms that short-faced bears such as the spectacled bear and Arctodus were adapted to and actively consumed vegetation.[28][62][23][71][67] This is affirmed by a lack of dental damage associated with carnivory amongst specimens of Arctodus.[95] Dental pathologies which have been found, such as incisor wear & supragingival dental calculus in a young individual from Missouri,[57] and cavities associated with carbohydrate consumption in individuals from the La Brea Tar Pits & Pellucidar Cave (Vancouver Island), further suggest an omnivorous diet for Arctodus simus.[87][95][18] Additional morphological adaptations include dexterous forelimbs and a partial false thumb, which would have assisted in foraging for vegetation,[78][86] along with the body size of large Arctodus simus (~1000 kg) matching or exceeding the expected upper limitations for a terrestrial carnivore (based on the more restrictive energy base for a carnivorous diet).[28][96][97]

While features of Arctodus simus morphology suggest herbivory, their close phylogenetic relationship to the omni-herbivorous spectacled bear presents the possibility that these traits may be an ancestral condition of the group. A browsing diet foraged from the canopies of trees and shrubs could have been difficult with the large and flattened rostrum and incisor build of Arctodus, while evidence of digging adaptations in Arctodus' forelimbs and claws (e.g. for rooting) is mixed.[46][49][77] Regardless, gross tooth wear suggests consumption of plant matter in the diet of Arctodus simus.[23][28] The diet of individuals from La Brea was most similar to the spectacled bear, which consumes tough leafy matter, seeded & pitted fruits and occasional protein. Arctodus' tooth wear remained consistent throughout the Pleistocene in La Brea. This indicated a less generalized diet than modern omni-herbivorous black bears, with none of the dental evidence of hard food consumption (such as carcasses or nuts) found in polar bears, black bears and hyenas.[23] Comparisons with the dental microwear of Ursus speleaus suggest dietary differences between the species, with cave bears consuming tougher vegetation than A. simus.[94] Although some researchers argue that herbivory should be more obvious from the isotope data gathered from northern Arctodus,[59] several Arctodus coprolites from The Mammoth Site in South Dakota and Meander Cave at Ni'iinlii'njik Territorial Park, Yukon contain Juniperus seeds (toxic to black & brown bears).[65][98]

Opportunistic carnivory

[edit]
Arctodus' closest living relative is the spectacled bear. Although mostly herbivorous, Tremarctos ornatus is on occasion an active predator.[99]

Evidence suggests that Arctodus also consumed meat, as evidenced by elevated nitrogen-15 isotope levels (corresponding to protein consumption) and bone damage on contemporary fauna. Additionally, elevated carbon-13 levels (corresponding to C3 resources) from many localities (Alaska,[100] California,[30][93] San Luis Potosí,[31] Texas,[101] Vancouver Island,[91][102] and the Yukon)[103] largely suggest browsers (and browsed vegetation) were the core of A. simus' diet.[47]

Arctodus simus' status as a predator is questioned by its gracility and lack of agility, which could have complicated predation upon adult mega-herbivores, and hindered the chasing down of nimbler prey.[74][76] Nevertheless, larger (male) Arctodus simus are suggested to have been more carnivorous than females, as very large brown bears may not be able to sustain themselves on a vegetarian diet.[102] Furthermore, the much larger frame of A. simus would have provided an advantage in disputes over carcasses.[20]

Studies establish that Arctodus simus would have had a varied diet across its range,[23] and was outcompeted and/or more herbivorous with increased competition from other predators.[87][102][100][93] The extinction of cursorial, hyper-carnivorous Borophagus and Huracan in the more open western North America left a vacant niche, possibly contributing to the evolution of A. simus (along with changes to the herbivore guild).[21][73]

Bone damage

[edit]
Arctodus may have found young proboscideans to be suitable prey.

The bite marks found on many bones of ground sloths (Northrotheriops texanus) and young proboscideans at Leisey Shell Pit in Florida matched the size of the canine teeth of Arctodus pristinus. It is not known if these bite marks are the result of active predation or scavenging.[1] Additionally, Arctodus pristinus was the most common large predator from Port Kennedy Cave, Pennsylvania, where the majority of mastodon remains were juveniles and likely represent accumulated prey.[104]

Arctodus simus has been found in association with proboscidean remains near Frankstown, Pennsylvania (juvenile mastodon), and at The Mammoth Site, South Dakota (Columbian mammoths). However, questions remain as to whether these finds determine a predatory or scavenging relationship, or whether they were simply preserved at the same deposit (possibly at different times).[65][105] On the other hand, a woolly mammoth specimen from Saltville, Virginia was likely scavenged on by Arctodus simus, as evidenced by a canine gouge through the calcaneus.[59] Several Columbian mammoth bones from a cave near Huntington Reservoir, Utah also record ursid gnaw marks attributed to Arctodus, with an Arctodus specimen preserved in association with the remains.[63]

Importantly, the canines of Panthera atrox overlap in size with Arctodus simus, complicating the identification of tooth marks.[59] However, this is not to discredit all tooth marks attributed to Arctodus, as damaged bones from near Tanana River, Alaska suggest that Arctodus transported megafaunal longbones back to a cave-like den and chewed on them,[106][68][107] at a time when lions had a limited overlap with Arctodus in Beringia.[108][87] Furthermore, a perforated peccary ilium from Sheriden Cave has also been hypothesized as being scavenged by Arctodus simus.[109] Bone damage on a cranial fragment (and possibly the humerus) of an Arctodus individual on Vancouver Island may have been due to cannibalism.[18][102]

Beringia

[edit]

Analysis of bones from Alaska showed high concentrations of nitrogen-15, a nitrogen isotope accumulated most strongly in carnivores. Although few specimens exist, there is currently no evidence of the same carbohydrate-related dental pathologies evident in southern populations of Arctodus simus.[87] Based on this evidence, A. simus was suggested to have been more carnivorous in Beringia than the rest of North America (with a preference for herbivores which consumed C3 vegetation, particularly caribou).[100][103][110] Increased carnivory may be due to a lower proportion of competitors and probably a lower availability of carbohydrate-rich food supplies across the year in the far northern latitudes.[87] Survival during the cold season for some northern populations of A. simus could have depended on the regular scavenging of ungulate carcasses, as is the case with Alaskan brown bears.[47][93] Ultimately, an opportunistic foraging strategy including up to 50% vegetation, and the meat of reindeer, muskox, carrion, and possibly some predators, is consistent with the isotopic data and the conclusions of the ecomorphological studies.[100]

Carbon isotope studies

[edit]

Although elevated nitrogen-15 levels have been argued to indicate carnivory, even the isotope data of the most carnivorous Beringian Arctodus overlapped with modern, typically omni-herbivorous brown bears from Europe, eastern Wyoming, and central Montana, demonstrating that isotope data cannot distinguish between hypercarnivores and omnivores which eat a significant amount of animal matter.[49][100] Studies are also complicated by a lack of compound-specific data,[93] and isotope data being variable in carbon-13,[111][112] and nitrogen-15 (due to individual/evolving prey and plant choices, the isotopic composition of the local environment, and nutritional stress).[103][113] Carbon-13 levels in Arctodus simus (enriched by both plants and prey matter) consistently reflect a diet based on C3 resources, typically found in closed to mixed habitats with at least some tree cover (such as open woodlands).[30][31][91][100][93][101] This includes C3 vegetation (leaves, stems, fruits, bark, and flowers from trees, shrubs, and cool season grasses)[28] and the browsers that fed on them, such as deer, camelids, tapir, bison and ground sloths.[31][47]

Studies
Location Age Carbon 13 (δ13C) Nitrogen 15 (δ15N) Results
Irvington, California Early

Pleistocene

−14.5 N/A Arctodus simus carbon isotope values from Irvington (along with Fairmead Landfill and McKittrick Tar Pits) are consistent with diet based on C3 resources.[30]
Fairmead Landfill, California Middle Pleistocene −11.9 N/A Initially proposed to consume Columbian mammoth, and large ungulates,[114] a 2015 study recalculated Arctodus' carbon isotope values to be closest to C3 vegetation consuming deer and mastodon.[30]
Cedral, San Luis Potosí Late Pleistocene −11.8 N/A This Arctodus individual had the strongest δ13C value of its local fauna. Arctodus' carbon isotope value was closest to values from the tapir and Hemiauchenia.[31]
Natural Trap Cave, Wyoming Late Pleistocene -13.1 N/A The Natural Trap specimens have the lowest δ13C of the Pleistocene fauna. Comparisons with contemporary Ursus suggest that the seasonality & individual choices within omnivorous diets could result in extreme isotope data, with each tooth not fully reflecting the total isotopic range consumed.[112]
Channel Islands, California Late Pleistocene -17.9 13.2 Nitrogen isotope signatures suggested a ~19% consumption rate of seals (along with bison and camels). Fossil was likely transported post-mortem from the mainland; a partial reliance on marine resources has been suggested to be as a result of a competitive carnivore guild on mainland California. The marine signal was in between island foxes and bald eagles, most closely resembling Late Pleistocene California condors.[93]
McKittrick Tar Pits, California Late Pleistocene -10.9 N/A This carbon isotope value was closest to deer, similar to the one inferred for the Cedral individual.[31][114]
Little Box Elder Cave, Wyoming Late Pleistocene -14.9 N/A Like Natural Trap Cave, the Little Box Elder Cave specimen had distinctly lower δ13C levels, being only higher than Ursus.[112]
Friesenhahn Cave, Texas Late Pleistocene -16.5 9.7 The Friesenhahn Cave specimen had a nitrogen-15 sample closest to the omnivorous striped skunk.[101]
Vancouver Island, British Columbia Late Pleistocene -18.9 10.6 A specimen from Cowichan Head, Vancouver Island, had isotopes suggesting a terrestrial diet at a relatively high trophic level.[91]
Fairbanks, Alaska Late Pleistocene -18.0 8.4 Nitrogen & carbon isotope data from several specimens suggests that Arctodus specialized on reindeer in central Alaska, both before and during the Last Glacial Maximum.[103]
Dawson, Yukon Late Pleistocene -18.5 9.9 Arctodus' nitrogen-15 levels are higher in the Yukon, suggesting a possibly even higher trophic level than other Arctodus in eastern Beringia. However, this contrast likely reflects subtle differences in the isotopic composition of local plants,[61][115] & muskox in the region, and possibly fellow predators and their kills, complimenting the consumption of reindeer.[100]

Hibernation

[edit]
A. simus specimens have been particularly plentiful from caves in the montane woodlands of the US Interior Highlands, such as the Ozarks.

Arctodus pristinus specimens have been found in caves such as Port Kennedy, Pennsylvania (where fossils from as many as 36 individuals have been found), and Cumberland Cave, Maryland, often in association with the black bear. This suggests a close association with the biome.[2][116]

According to a 2003 study, in karst regions, fossils of Arctodus simus have been recovered almost exclusively from cave sites.[57] In the contiguous United States, that ~38% of all sites are from caves (possibly ~50% in western USA)[54] suggests a close association between this species and cave environments. Metabolic denning (hibernation/torpor) is unclear in Arctodus. Like polar bears, male and unmated female A. simus may have forgone denning, leaving maternal denning by females as the preferred explanation behind the recovery of the small, yet relatively complete individuals recovered from caves.[57][40] However, to date, there are no records of adults with associated offspring from caves.[58] Regardless, Arctotherium angustidens, a fellow giant short-faced bear, has been recovered from a cave in Argentina with offspring.[117]

At Riverbluff Cave, the most abundant claw marks are from Arctodus simus. They are most abundant at the bear beds and their associated passageways, indicating a close relationship with denning.[84] Numerous "bear" beds often preserve Arctodus simus and both Pleistocene and modern American black bears in association (U.a. amplidens and U. a. americanus)- such deposits have been found in Missouri, Oklahoma and Potter Creek Cave, California. These mixed deposits are assumed to have accumulated over time as individual bears (including Arctodus) died during winter sleep.[5][118][119] Furthermore, environmental DNA suggests that Arctodus and black bears shared a cave in Chiquihuite cave, Zacatecas.[17] At Labor-of-Love Cave, Nevada, both American black bears and brown bears have been found in association with Arctodus simus. A study in 1985 noted that sympatry between Arctodus and brown bears preserved in caves is rare, with only Little Box Elder Cave, Wyoming and Fairbanks II, Alaska hosting similar remains.[28][51]

Paleoecology

[edit]

Arctodus pristinus

[edit]
A reconstruction of Arctodus pristinus, from the Bishop Museum of Science and Nature, Florida.

Endemic to the late Blancan faunal stage and Irvingtonian faunal stage, Arctodus pristinus was a relatively large tremarctine bear.[1] Sometimes referred to as the eastern short-faced bear,[120] A. pristinus has been found in Florida,[2] Kansas,[7] Maryland,[7] New Mexico,[121] Pennsylvania,[54][116] South Carolina,[122] and West Virginia in the US,[7] and Aguascalientes in Mexico.[123] Possible remains have also been recovered from Arizona.[7][124] A. pristinus is particularly well known from Florida, especially from the Leisey Shell Pit.[125] Like A. simus and other tremarctine bears, A. pristinus had adaptations for herbivory, and was likely largely herbivorous itself,[2] although Arctodus has been suggested to be generally more carnivorous than contemporary bears.[1][38]

Eastern North America

[edit]

Arctodus pristinus is considered a biochronological indicator for the period between the Late Blancan and late Irvingtonian periods of Pleistocene Florida- more fossils of Arctodus pristinus are known from Florida (about 150) than anywhere else.[2] In the Early Pleistocene of Blancan Florida, the Santa Fe River 1 site (~2.2 Ma), which Arctodus pristinus inhabited,[1][2] was a fairly open grassland environment dotted with karst sinks and springs and dominated by longleaf pine flatwoods. Arctodus pristinus co-existed with terror birds, sabertooth cats, giant sloths (Eremotherium, Megalonyx, Paramylodon), giant armadillos (Glyptotherium, Holmesina, Pachyarmatherium), gomphotheres, hyenas, canids (Borophagus, Canis lepophagus), peccaries, llamas, dwarf pronghorns, and three-toed horses. Smaller fauna included condors, rails, ducks, porcupines, and alligators.[126][127]

Arctodus simus

[edit]
By the Late Pleistocene, Arctodus simus was present in most physiographic regions of the Nearctic realm.

Evolving from the smaller A. pristinus in the early Irvingtonian faunal stage,[7][27] scholars today mostly conclude that Arctodus simus was a colossal, opportunistic omnivore, with a flexible, locally adapted diet akin to the brown bear.[47][62][18][93][39] If Arctodus simus wasn't largely herbivorous,[2][28] the scavenging of megaherbivore carcasses, and the occasional predatory kill would have complimented the large amounts of vegetation consumed when available.[47][49][18][128]

Sometimes referred to as the bulldog bear,[129][130] or great short-faced bear,[15][131] Arctodus simus has been recovered from a comparatively small number of finds in relation to other large carnivorans, with the species suggested to have lived in low population densities.[17] Matheus argues that unlike other Nearctic carnivorans, A. simus did not appear to have an ecological equivalent ("super-huge bear") in the Palearctic realm.[55]

Arctodus simus was initially restricted to the western United States during the Irvingtonian.[36][37][38] However, in the Rancholabrean faunal stage, A. simus expanded its range from southern Canada to central Mexico in the west, and to Pennsylvania and Florida in the east.[7][12][20][132] A. simus also inhabited eastern Beringia at times, with finds today spanning from northern Alaska to the Yukon.[17][20][132] Based on the wide distribution of the species, Arctodus simus inhabited a diversity of climatic conditions and environments.[20][28][87] A 2009 study examining megafaunal extinctions in Northern America noted 12 records (<40,000 BP) of Arctodus simus from the Intermontane Plateaus, 7 from the Pacific Mountain System, 6 each from the Interior Plains and Interior Highlands, 3 each from the Atlantic Plains and Rocky Mountain System, and 1 from the Appalachian Highlands.[133]

A. simus was relatively plentiful in western North America, with over 50% of specimens from the western contiguous United States (<40,000 BP).[33][87] Arctodus simus was integral to what has been referred to as the Camelops fauna, or alternatively Camelops/"Navahoceros" fauna, a faunal province centered in western North America. The Camelops fauna was also characterized by shrub-ox, prairie dogs, dwarf pronghorns, Shasta ground sloths, and American lions. The diverse flora of the Camelops faunal province included montane conifers and oak parklands, shrub and grassland that stretched across the North American Cordillera south of Canada, to the Valley of Mexico. This faunal province supported a variety of large grazing and browsing mammals.[29][134][135]

Western Mountains

[edit]
Arctodus simus inhabited Californian savannas for around a million years.

The Pacific Mountain System seems to represent a cradle of evolution for Arctodus simus. The earliest confirmed finds of Arctodus simus are from Irvington, California,[136] which are at least 780,000 years old, but may be older than 1.2Mya.[27] Other Irvingtonian age sites come from California, such as Elsinore,[137][138] Fairmead,[139] and Murrieta.[36] Older yet disputed remains come from El Casco (1.4Mya).[36][140]

Despite the shift to aridified, mixed C3-C4 habitats between the Early and Late Pleistocene of the Central Valley (~1Mya to ~15,000 BP), Arctodus simus remained consistent with the consumption of C3 resources. Dire wolves and Arctodus simus were ever present members of the local predator guild throughout the Pleistocene, whereas jaguars, Homotherium, Miracinonyx and Smilodon (Fairmead & Irvington) transitioned to Panthera atrox and coyotes (McKittrick Tar Pits).[30] Although Arctodus could have hunted other closed habitat browsers such as deer (Cervus & Odocoileus), camelids (Hemiauchenia & Camelops), Paramylodon, and peccaries,[30] specimens collected from the La Brea Tar Pits suggest A. simus preferred a herbivorous diet. A. simus is particularly famous from fossils found in the La Brea Tar Pits, with 33 individuals recovered (the most of any locality).[141][23][142] As only one juvenile has been found from La Brea, A. simus is suggested to have been solitary.[128] Many more finds come from across California,[7][5][143] Vancouver Island,[18][91] and Washington,[91] where the semi-arid woodland/scrub transitioned to forest-steppe,[144] and open grasslands/heath.[91]

Comparatively, the Rocky Mountain System had the fewest number of specimens of Arctodus simus in western North America.[33] However, one of the youngest dated Arctodus simus is from a cave near Huntington Reservoir, Utah, which sits at an elevation of 2,740m (~9,000 ft). The central and southern Rocky Mountains may have acted as refugia for boreal parkland megafauna from the plateau such as Arctodus simus,[63][29] with the Huntington specimen being the only confirmed extinct megafauna dated to the Younger Dryas of the Great Basin.[145] Other remains have been found from Wyoming (such as Natural Trap Cave),[146][147] and Montana.[148][149]

Intermontane Plateaus

[edit]
A reconstruction of Rancholabrean New Mexico (White Sands).

The Intermontane Plateaus had the highest number of Arctodus simus specimens south of the ice sheets.[33][133] The region has yielded some of the largest specimens of A. simus, including what was once the largest specimen on record, from Salt Lake Valley, Utah.[53] Disputed Irvingtonian remains from eastern California (Victorville and Vallecito Creek) may be as old as 2Mya.[7][150][151]

In contrast with other parts of North America, the plateaus received more rainfall during the Late Pleistocene, as glacially cooled air collided with hot desert air. As a result, this greatly expanded the range of subalpine parkland, piñon-juniper & ponderosa woodlands, sagebrush grasslands and pluvial lakes where desert exists today.[145][144][54][152] The mid-Wisconsian U-Bar Cave, New Mexico, was vegetated by sagebrush, grasses, and woodlands. Notable fauna which lived alongside Arctodus simus included Shasta ground sloth, shrub-ox, pronghorns (Stockoceros, Capromeryx), Camelops, Odocoileus, horses, Lynx, puma, black bear, mountain goats, prairie dogs, and Stock's vampire bat.[32][153] Dire wolves were also found in association with Arctodus simus, and both species are the most common large carnivorans of Rancholabrean New Mexico.[54] Beyond Utah and New Mexico,[54][154][155][156][157][158] other important US specimens have also been found in Arizona,[7] eastern California,[7][159][160] Idaho,[7] Nevada,[161] and eastern Oregon.[162][163][164]

The Intermontane Plateaus extended into central Mexico, with the Mexican Plateau sharing the Late Pleistocene mesic savanna and piñon–juniper woodland ecoregion with the southwestern USA.[165][166] While Arctodus was limited to the Mexican plateau, the typical tropical thorn scrub and scrub woodland of the plateau was seemingly prime habitat for tremarctine bears.[33][144][167] An Arctodus simus individual from Cedral, San Luis Potosí, inhabited closed vegetation, based on the individual's δ13C signature. Consuming C3 resources, its diet may have incorporated local C3 specialists such as tapir, llamas, camels, and Shasta ground sloth along with browsed vegetation. The site, incorporating trees, herbs and cacti, hosted an open gallery forest near grassland or scrub with a humid climate.[31] Similar highland remains have been recovered from Jalisco,[168] Michoacán,[167] Puebla,[7] State of Mexico,[169][170] and Zacatecas.[17]

Interior Plains

[edit]

The Interior Plains were composed of temperate steppe grassland,[144] and among the specimens yielded from this region is one of the largest Arctodus simus currently on record, from the banks of the Kansas river.[171] The late Irvingtonian Doeden gravel pits in Montana preserves an open grassland habitat, with riparian woodlands, and likely some shrublands.[172] Arctodus simus co-existed with ground sloths (Megalonyx, Paramylodon), Pacific mastodon, camels, and Bootherium.[173][174][37] As bison were yet to migrate into North America, Columbian mammoths and horses dominated these early Illinoian grasslands.[175] Additional Irvingtonian remains are from Kansas, Nebraska and Texas.[36][38][7]

Arctodus also roamed the southern mixed grasslands of Texas.

In the Rancholabrean age, Arctodus simus, grey wolves and coyotes were part of a predator guild throughout the great plains, and were joined by Columbian mammoths, camels, Hemiauchenia, and American pronghorns. While the northern plains aridified into cold steppe (e.g. Mammoth site, South Dakota),[176] the southern plains were a parkland with riparian hackberry forests, and large expanses of mixed grass prairie grasslands grading into wet meadows, with limited seasonality. In the south (Lubbock Lake, Texas), this fauna was joined by Smilodon, dire wolves, grey fox and red fox, preying upon prairie dogs, horses (Equus & Haringtonhippus), peccaries, Odocoileus, Capromeryx, Bison antiquus and Holmesina.[176][177] Beyond Texas,[178] Arctodus has also been found in Iowa,[179] Kansas,[7][180] Nebraska,[7] and southern Canada (Alberta & Saskatchewan),[181][182][183] which when unglaciated, would have formed a tundra ecosystem with an ice-free corridor to Beringia.[184]

In the lowlands of the eastern Interior plains, the plains transitioned to closed habitat. At the terminal Pleistocene Sheriden Cave, Ohio, a mosaic habitat consisting of marsh, open woodland, and patchy grassland was home to Arctodus simus, Cervalces scotti, caribou, peccaries (Platygonus, Mylohyus), giant beaver, porcupine, and American pine marten.[185][109] Similar remains have been found in Indiana,[45] and Kentucky.[186][187]

Interior Highlands

[edit]

To the south, the Interior Highlands had a very high density of Arctodus simus specimens (second only to the black bear),[33][87] due to the high rate of preservation in the cave-rich region. Sympatry between the two species is most apparent in Missouri- Arctodus simus has been found in association with black bears at Riverbluff, Bat and Big Bear caves.[188] Big Bear Cave preserves fossilized hair associated with Arctodus.[57] During the Last Glacial Maximum, both bears were joined by dire wolves, coyotes, jaguars, snowshoe hare, groundhogs and beavers at Bat Cave, which also records thousands of Platygonus remains. These fauna inhabited well-watered forest-grassland ecotone with a strong taiga influence, although the region did occasionally cycle through drier, grassier periods. These open woodlands were dominated by pines and spruce, and to a lesser extent by oaks.[189][190][191][192][193] Additional finds have been recovered from Oklahoma.[118][119]

Eastern USA

[edit]
Lake Rousseau, Florida, is the south-easternmost locality which Arctodus simus is known to have inhabited.

Compared to other regions, Arctodus simus was relatively rare in eastern North America.[20][33][87] To the north, the Appalachian Highlands were dominated by taiga.[144] Post-LGM Saltville, Virginia, was a mosaic of grassy/herb laden open areas intermixed with open canopy boreal woodlands (oaks, pines, spruce, birch, firs) and marshes. Inhabiting in this C3 resource dominated environment were Arctodus simus, mastodon, (southernmost) woolly mammoths, Bootherium, horses, caribou, Megalonyx, dire wolves, beavers, Cervalces, and a variety of warm-adapted reptiles, suggesting a more mesic and less seasonal climate than today. Heavy bone damage on a mammoth carcass by both dire wolves and Arctodus suggests a potentially competitive scavenging relationship [194][59] Beyond Virginia,[58] additional remains have been found in Pennsylvania.[7][105]

To the south, the subtropical Atlantic Plains covered a great expanse of lowland, from the open deciduous woodlands of the Atlantic coast, to the semi-arid woodland/scrub of Florida, to the spruce-fir conifer forests and open habitat of the Gulf Coastal Plain. Although scarce, this contrast of habitats highlights the adaptability of Arctodus simus. At the Rainbow River and Lake Rousseau localities in Rancholabrean Florida, three Arctodus simus specimens have been recovered, alongside Smilodon, dire wolves, jaguars, ground sloths (Megalonyx, Paramylodon), llamas (Hemiauchenia, Palaeolama), Vero's tapir, giant beaver, capybara, Holmesina, horses, Bison antiquus, mastodon, Columbian mammoths and Tremarctos floridanus, in a climate similar to today's. Furthermore, the abundance of black bears, and particularly Tremarctos floridanus in Florida, has led to a theorized niche partitioning of ursids in Florida, with Tremarctos floridanus being herbivorous, and black bears and Arctodus simus being omnivorous, with Arctodus being possibly more inclined towards carnivory.[20] Additional finds of south-eastern Arctodus simus are from Alabama,[195] Arkansas,[196] Mississippi,[197][198][199] South Carolina,[200] and Texas.[64][201]

Beringia

[edit]
Arctodus is suggested to have had a kleptoparasitic relationship with Beringian wolves, akin to modern wolves and brown bears.

Largely isolated by the Cordilleran and Laurentide ice sheets, Beringia is considered ecologically separate to the rest of North America, being largely an extension of the mostly open and treeless Eurasian mammoth steppe.[202] However, the occasional opening of an ice-free corridor, and the migration barrier of the Beringian gap, meant that eastern Beringia (Alaska and the Yukon) supported a unique assemblage of fauna, with many endemic North American fauna flourishing.[75] Currently, all specimens of A. simus in Beringia have been dated to a 27,000 year window (50,000 BP - 23,000 BP) from eastern Beringia,[108][18][7][56] while additional undated remains may be of Sangamonian age.[203][55] Unlike contemporary Beringian carnivorans, A. simus apparently never inhabited western Beringia (and therefore Asia).[55] The largest known skull of A. simus was recovered from the Yukon, and may represent the largest specimen known.[49][204]

The North Slope of Alaska <40,000 BP (Ikpikpuk and Titaluk rivers) preserves an upland and floodplain environment, with horses, bison then caribou being the most populous herbivores, and woolly mammoths, muskox, elk and saiga antelope more scarce. Cave lions, bears (Ursus arctos and Arctodus simus), and Beringian wolves made up the megafaunal predator guild.[205][206] Isotope data implies that caribou and muskox were principal components of the carnivorous portion of Arctodus simus' Arctic diet, suggesting that the warmer, wetter vegetation on the margins of the dry mammoth steppe (similar to the moist acidic tundra vegetation which dominates today) was the preferred habitat of Arctodus in Beringia.[100][205]

Additionally, upon the flooding of the Bering Strait and expansion of moist tundra and peatlands in eastern Beringia during MIS-3, lions, brown bears and Homotherium went regionally extinct ~35,000 BP, whereas wolves and Arctodus persisted. Simultaneously, most megafaunal herbivores in Beringia experienced population bottlenecks, whilst mammoth populations steadily declined. This restriction of prey and habitat could explain the extinctions. However, genetically distinct cave lions and brown bears appear in MIS-2 circa the extinction of Arctodus in a re-emerged Beringia ~23,000 BP, opening up the possibility that some level of competition was at play.[108][100][207][208][209] The idea that Arctodus had a kleptoparasitic relationship with wolves and Homotherium in Beringia has been explored,[100] with the additional possibility that Arctodus successfully competed against brown bears and Homotherium for access to caribou pre-LGM.[103]

The local extinction of Arctodus in Beringia ~23,000 BP (possibly due to sharp climatic cooling associated with Heinrich Event-2),[108][18] was much earlier than in other parts of its range. While recolonized by cave lions and brown bears from Eurasia, Arctodus did not repopulate Beringia once the ice-free corridor to the south re-opened later in the Pleistocene.[108][210]

Map of fossil localities

[edit]
Arctodus is located in North America
American Falls (Hop-Strawn Pit, Cedar Ridge, 26,500 ± 3500 BP)
Birch Creek (34,974 ± 652 BP)
Bonner Springs (Kansas River, 10,921 ± 50 BP)
Chiquihuite Cave (11,419 ± 34 BP)
Cueva Quebrada (12,280 ± 170)
Fairbanks (Cleary, Cleary Creek, Dawson Cut, Engineer Creek, Ester, Ester Creek, Eva Creek Mine, Gold Hill, Goldstream, No.2 G-Strip Area, Upper Cleary River Beds, 39,565 ± 1126 BP - 20,524 ± 180 BP?)
Friesenhahn Cave (10,814 ± 55 BP)
Fulton County (11,040 ± 310 BP)
Gold Run Creek (26,040 ± 270 BP)
Huntington Dam (10,976 ± 40 BP)
Ikpikpuk River (27,160 ± 280 BP)
Island Ford Cave (34,080 ± 480 BP)
La Brea Tar Pits (35,370 - 26,427 cal. BP (≤50,000?))
Meander Cave (37,500 cal. BP?)
Natural Trap Cave (20,220 ± 150 BP)
Pellucidar Cave (11,615 ± 30 BP)
Potter Creek Cave (type locality (+ Samwell Cave & Stone Man Cave), 12,650 ± 350 BP)
Rainbow Beach (21,500 ± 700 BP)
Salt Lake Valley (Silver Creek/Bonneville, 12,650 ± 70 BP)
Saltville Valley (14,853 ± 55 BP)
San Miguel Island (Daisy Cave, California Channel Islands, 14,130 ± 70 BP)
Sheriden Cave (11,566 ± 40 BP)
Sixtymile River (44,240 ± 930 BP)
The Mammoth Site (26,075 ± 975 BP)
Three-Forks Cave (Gittin' Down Mountain, 34,063 ± 460 BP)
Titaluk River (42,600 ± 2,200 BP)
Airport Lane
Alameda Tube
Albuquerque Gravel Pits
Atepetzingo (Rancho de Tepetzingo)
Beaver Crossing (unknown age)
Beemer & West Point (Cuming County Wet Gravel Pits)
Big Bear Cave, Bat Cave, Carroll Cave, West Cave
Big Bear Site ("Arctodus site", Blackwater Draw)
Bitter Springs Playa (Rogers Ridge, Fort Irwin)
Blacktail Cave
Box Butte Creek
Burnet Cave (Rocky Arroyo)
Cedar Creek (Black Belt, c.f. simus)
Cedral
'Chat' (Chatanika River)
Chicken Creek (Lost Chicken Creek?)
Clover Bar (Edmonton)
Conkling Cavern?
Cooper River
Copper Mine
Cripple Creek
Dalhart
Diamond Valley
Drews Gap (footprints, Lakeview)
Duck Flat
Fern Cave
Fort Qu' Appelle (Bliss Gravel Pit-Echo Lake Gravel)
Fossil Lake
Frankstown Cave
Gatesville (Coryell County, Ursidae c.f. A. simus)
Glass Cave
Hall's Cave
Isleta Caves
Jaguar Cave
Jinglebob
Keams Canyon
Kotzebue
La Cinta Portalitos
Labor-of-Love Cave
Lake San Agustin (White Lake)
Lebret
Lilian Creek
Little Box Elder Cave
Lubbock Lake
Manix Lake (Camp Cady)
Maricopa Tar Seeps
Moore Pit (Hill Shuler/ Trinity River)
Old Crow Flats
Oregon Caves?
Oso Cave
Pendejo Cave?
Powder Mill Creek Cave, Round Spring Cave
Proctor Cave
Prospects Cave
Red Willow local fauna (Upper Republican River)
Red Willow local fauna (McCook, unknown age)
Riverbluff Cave
San Juan Island
Schultz Cave
Seale Pit (Hill-Shuler/Trinity River)
Selawik
Skeleton Cave
Spalding Site
Tequixquiac
The Bar (Central Mississippi Alluvial Valley)
Troublesome Creek
Tofty (Tofty Placer District)
U-Bar Cave
Valsequillo
Wasden Site (Owl Cave)
Wright Materials North
Zacoalco
Arkalon
Cass County
Doeden Gravel Pit (Yellowstone River)
El Casco fauna? (San Timoteo)
Elsinore
Fairmead Landfill
Gordon
Irvington
Murrieta (Riverside)
Rock Creek (Briscoe County)
Rushville
Vallecito Creek? (Anza-Borrego)
Victorville (cf. simus)
111 Ranch (Arctodus sp.)
Aguascalientes (Cedazo)
Apollo Beach, Leisey Shell Pit 1, Leisey Shell Pit 1A & Leisey Shell Pit 3
Bass Point Waterway, Rigby Shell Pit, Venice Beach
Coleman 2A
Crystal River Power Plant (Inglis 1A & Inglis 1B)
Cumberland Bone Cave
Haile 16A
Kissimmee 6
La Union (Mesilla Basin Fauna B)
Lost World Caverns (Grapevine Cave)
McLeod Limerock Mine
Morgan River
Myrtle Beach
Port Charlotte
Port Kennedy Cave
Santa Fe River 1
Sebastian Canal 2
Stout's Ranch (Saw Rock Canyon)
Whitlock Oil Well (San Simon Creek, Arctodus sp.)
Ashley River (Bee's Ferry, "Wando Formation"), Cooper River, Ladson Formation, Walrus Ditch Local Fauna
Hay Springs
Lake Rousseau & Rainbow River
McKittrick Tar Seeps (11,040 ± 310 BP)
Perkins Cave (16,910 ± 50 BP)
Cowichan Head (22,750 ± 140 BP)
La Sena (19,487 ± 95 BP)
Dawson (Canyon Creek, Dawson City, Eldorado Creek, Hester Creek, Lower Hunker Creek, Ophir Creek, Quartz Creek, 49,800 cal. BP - 22,417 ± 452 BP)
White Sands National Park (footprint, ~18,500 BP)
Interactive distribution map of Arctodus (hover over dots for locality information)

Legend: A. pristinus (Late Blancan / Irvingtonian)

Early/Middle Pleistocene (Irvingtonian) A.simus

Late Pleistocene (Rancholabrean) A. simus

Radiocarbon dated A.simus (14C Date (1σ), ≤50,000 BP)

Relationships with other bears

[edit]

Arctodus pristinus

[edit]

In the Early Pleistocene, Arctodus pristinus was much more populous the south-east of North America, whereas the black bear was more common in the north-east.[211] The black bear has inhabited North America since at least the Middle Pleistocene,[102] while Tremarctos floridanus, a tremarctine bear inhabiting western North America at the time, is very similar to A. pristinus in terms of size, skeletal anatomy, and dietary preferences.[2]

Despite this, generally speaking large tremarctine fossils from the Early and Middle Pleistocene of Florida are considered to be A. pristinus, whereas those from the Late Pleistocene of Florida are considered to be T. floridanus. Indeed, black bears and Tremarctos floridanus are believed to have only colonized Florida with the extinction of A. pristinus (both of which only appear in Florida in the Late Pleistocene), however, T. floridanus could yet still be found from older sites in Florida.[2] T. floridanus was possibly an ecological replacement of A. pristinus, with T. floridanus finds being widespread in Rancholabrean Florida and the wider southeastern United States.[2][25][33]

Arctodus simus

[edit]
Arctodus simus reconstruction at the Hot Springs Mammoth Site, South Dakota.

The most commonly accepted ecological parallel of Arctodus simus in scientific literature is the brown bear.[47][62][18] Both brown bears and Arctodus simus exhibit a high degree of dietary variability, and while largely herbivorous, meat can be an important dietary element to certain populations of both species.[100] Additionally, the potential of habitual kleptoparasitism is often noted in Arctodus, with brown bears being opportunistic, curious, and regularly stealing kills from smaller predators.[72][100] One past theory behind the extinction of Arctodus simus is that A. simus may have been out-competed by brown bears as the latter expanded southwards from eastern Beringia ~13,000 BP, and gradually established itself in North America.[51]

However this has been refuted as new dates establish an extended coexistence, with some isolated A. simus remains being re-evaluated as brown bears.[108][18] Brown bears (along with lions, bison and red foxes) first emigrated to North America via Beringia during the Illinoian Glaciation, with brown bears first arriving between ~177,000 BP and ~111,000 BP in eastern Beringia.[108] Genetic divergences suggest brown bears first migrated south during MIS-5 (~92,000 - 83,000 BP) upon the opening of the ice-free corridor,[108][102] with the first fossils being near Edmonton (26,000 BP).[18] On a continent-wide scale, although the brown bear and Arctodus simus were sympatric at times as brown bears spread into North America, Arctodus simus may typically have dominated competitive interactions, and displaced brown bears from specific localities.[18] Additionally, Arctodus' prolonged co-existence with black bears may have put significant constraints on the black bear's evolution.[15]

At the end of the Pleistocene, one reason brown bears persisted where Arctodus simus went extinct was because Arctodus may have been less flexible in adapting to new and rapidly changing environments that impacted the availability or quality of food and habitat.[18] Brown bears and Arctodus have been discovered together in Alaska (then Beringia) between 50,000 BP and 34,000 BP,[108] and in later Pleistocene deposits in Vancouver Island, California, Wyoming and Nevada.[7][18]

Beringia

[edit]

Isotope values (δ13C and δ15N) in numerous Beringian Arctodus simus specimens suggests A. simus usually occupied a higher trophic level compared with invading brown bears. While some Beringian brown bears consumed salmon, data from Beringian specimens of Arctodus clustered much more tightly, and suggested that only terrestrial sources of meat were important for Beringian Arctodus.[61] The forcing of a smaller bear into a more herbivorous diet has been compared to the modern relationship between brown bears and American black bears.[72][100] Where they overlap, black bears take the lower trophic niche, with lower population densities, much smaller territorial ranges, and seasonal migrations.[102] That Arctodus simus (along with local climate change) may have excluded brown bears from eastern Beringia from ~34,000 to ~23,000 BP further suggests that Arctodus may typically have been dominant over brown bears.[207][208] When Arctodus went extinct in Beringia ~23,000 BP, brown bears recolonized Beringia, but had more carnivorous diets than their Beringian kin pre ~34,000 BP. This bolsters the idea that these bears competed for similar resources and niches.[108][18] Extinction and repopulation is further evidenced by the high genetic (mitochondrial) diversity of Beringian brown bears in contrast with Beringian Arctodus simus. This contrast in genetic diversity has also been hypothesized to suggest that while female brown bears have a permanent home range, female Arctodus simus may not have (at least not to the same extent).[92][108]

The brown bear was a direct competitor of Arctodus simus.

Vancouver Island

[edit]

Brown bears, black bears and Arctodus simus all co-existed on Vancouver Island once the island de-glaciated ~14,500 BP.[102][18] According to an isotope analysis, all three bears relied on terrestrial resources, Arctodus holding an intermediate trophic position between the brown and black bears. This may be an underestimate, as the Arctodus specimens from Vancouver Island are believed to be female; as per brown and black bears, female A. simus may have had a significant decrease in protein consumption compared with male A. simus when co-existing with brown bears. Additionally, an analysis of Arctodus' data suggested that when consuming protein, meat was preferred.[102] While niche-partitioning on Vancouver Island was possible, both Arctodus simus and brown bears appeared to have preferred more open habitats.[102]

Convergent evolution

[edit]

Both giant short-faced bears Arctodus simus and Arctotherium angustidens reached huge body sizes, in an example of convergent evolution.[21] However, beyond gigantism, there are notable differences between the species. Not only did Arctotherium angustidens reach a higher maximum weight (an exceptional specimen was calculated at ~1,670 kilograms (3,680 lb)), A. angustidens was a much more robust animal, in contrast with the gracile Arctodus simus.[41] Excluding the exceptional specimen, Arctotherium angustidens had been calculated to a weight range between 1,200 kilograms (2,600 lb) and 412 kilograms (908 lb),[212][47] with the largest specimens of either species being said to be comparable to one another.[212][62] The panda-relative Agriotherium africanum has also been suggested to share ecomorphological convergences with Arctodus simus.[49] Together with great size, the two species converged on several adaptations, including a skull with a short broad rostrums, premasseteric fossa on the mandible, possible carnassial shears (P4 and m1), and long limbs (relative to body length). These features were also shared by other extinct bears (Agriotherium, Huracan and Arctotherium bonariensis).[49] However, while Agriotherium and Huracan have definitive adaptions for meat-heavy diets stemming from a running, predatory lifestyle, Arctodus simus lacks similar adaptations beyond proportionally longer limbs.[73]

Interactions with humans

[edit]
The Clovis people are the first known culture to have interacted with Arctodus.

One documented interaction with Clovis people is present at the Lubbock Lake Landmark, Texas. A likely already deceased Arctodus simus was processed for subsistence (butchery marks indicated skinning, de-fleshing and disarticulation) and tool production, much in the same way as a mammoth carcass (~13,000 BP / 11,100 14C BP ).[213][214] Additionally, other remains of the Arctodus simus have been found in association with Paleo-Indian artifacts in Sheriden Cave, Ohio,[185][109][215] and Huntington Dam, Utah,[63] with an A. simus footbone fragment from Spalding, Idaho also being charred.[216][217] The direct relationship between humans and some associated Arctodus remains has been debated.[218][219][220] Human hunting and butchery of large megafauna, particularly mammoths and mastodon, would likely have put people in competition with Arctodus simus. Defense against these large bears and the abandonment of carcasses are plausible outcomes,[18] along with the possible caching and disposal of carcass remains underwater to mask its odor from Arctodus.[221]

Migration barrier hypothesis

[edit]

In the late 1980s, Val Geist hypothesized that "specialist, aggressive, competitive Rancholabrean fauna" such as Arctodus were a barrier for humans (along with other Siberian megafauna such as moose, grey wolves and brown bears) when migrating into North America (both Beringia and below the ice sheets).[222] Male A. simus were the largest and most powerful carnivorous land mammals in North America, with the potential specialization in obtaining and dominating distant and scarce resources. Humans in this hypothesis, though familiar with brown bears, would not have been able to avoid predation or effectively compete with Arctodus simus and other large Pleistocene North American carnivores, making human expansion difficult in Beringia and impossible south of the ice sheets.[18][72][55] However, this theory has never been accepted by anthropologists.[55] Paul Matheus argues that there were negligible ecological differences across the mammoth steppe, and that humans successfully competed against and even hunted territorial cave bears, cave hyenas, cave lions, leopards, tigers and wolves in Eurasia before reaching eastern Beringia, making the solitary Arctodus an unlikely impediment to expansion.[55] Indeed, new dates establish an extended co-existence of humans and megafauna such as Arctodus across North America.[223][224][225][226]

Beringia

[edit]
Beringia during the Last Glacial Maximum.

Humans migrated to North America via the Siberian mammoth steppe, arriving at eastern Beringia (Alaska and the Yukon). However, the migration was halted at the North American Ice Sheet, which separated Beringia and southern North America for most of the Late Pleistocene.[227] Both humans and Arctodus are first dated to ~50,000 BP in Beringia, both from sites in the Yukon, and co-existed until Arctodus went extinct in Beringia ~23,000 BP during the Last Glacial Maximum. This co-existence continued through the regional extinction of other Beringian predators such as cave lions, brown bears and saber-tooth cats.[108] Important sites of pre-LGM human occupation in Beringia include Old Crow Flats and the Klondike,[228][229] Kuparuk River Valley,[230] and the Bluefish Caves.[231][232]

Contiguous North America

[edit]

The human colonization of North America south of the ice sheets further disproves the idea that Arctodus was a migration barrier. The earliest universally accepted pre-Clovis site south of Beringia are the White Sands footprints in New Mexico, dated to ~22,000 cal. BP.[223] Other pre-LGM sites across the Americas, such as Chiquihuite Cave,[233][224] Valsequillo,[234] El Cedral,[235] Santa Elina,[225] Gault,[236] and Hartley Mammoth Site,[237] affirm that humans proliferated alongside megafauna (such as Arctodus) in southern North America for more than ten thousand years.[224][226][236][237][238] Humans were definitively widespread across the Americas by at least 15,000 BP.[18][226]

Extinction

[edit]

Arctodus pristinus

[edit]

Arctodus pristinus went extinct in the Middle Pleistocene (300,000 years ago),[20] being last recorded from the Coleman 2A site, Florida.[239] The evolution of Arctodus simus, competition with Tremarctos floridanus and black bears, and possibly the transitioning of Pleistocene Florida from a hot, wet, densely forested habitat to a still hot, but drier and much more open biome are thought to be factors behind the gradual disappearance of Arctodus pristinus in the late Irvingtonian faunal stage.[20][33] There are dubious records of A. pristinus in South Carolina and California from the Late Pleistocene,[69][240] however these are heavily disputed.[122][93] Modern research establishes A. pristinus as existing between the Pliocene-Pleistocene boundary and the Middle Pleistocene.[2][20][122]

Arctodus simus

[edit]
Skeletal reconstruction of Arctodus simus.

With the extinction of Arctodus pristinus, Arctodus simus became the final representative of the genus. Arctodus simus went extinct around 12,800 years ago, and is one of the most recently dated megafauna to go extinct in North America, being reliably dated to within the Pleistocene-Holocene boundary (13,800 BP - 11,400 BP).[241][133][242] Both local and regionalized dietary flexibility has been a factor suggested for the species' longevity.[87]

Various factors, including the depletion in number of large herbivores,[50][46] the diminishing nutritional quality of plants during climate change, and competition with fellow omnivores (humans and brown bears) for food resources, have been suggested as the cause of Arctodus simus' extinction.[213] However, multiple studies put doubt on brown bears being culpable in Arctodus simus' extinction, with the brown bear being more of an ecological replacement that was more adaptable to change.[33][18][46] Moreover, there is no systematic evidence that humans hunted large extinct Pleistocene carnivores in North America, and no clear indication of direct human involvement in the extinction of Arctodus simus.[18] Additionally, dental wear evidence from Rancho La Brea does not suggest that food shortages were to blame for the demise large bodied carnivorans such as Arctodus simus.[23]

Climate change

[edit]

Of the factors discussed, vegetation shifts in the latest Pleistocene may have been particularly unfavorable for Arctodus simus, due to a reduction of quality foraging for subsistence. For example, on Vancouver Island (~13,500 BP), vegetation changed rapidly from open woodlands with abundant lodgepole pine to increasingly closed forests with shade-tolerant spruce, mountain hemlock, and red alder. These changes, effective by ~12,450 BP, point toward cool and moist conditions during the Younger Dryas stadial. Closed forests continued to expand in the early Holocene. Even though Arctodus simus was not restricted to open areas and could inhabit in different environments, the timing of the regional shift from an open pine woodland habitat to a densely forested vegetation implies that these vegetation changes contributed to the local extinction of Arctodus simus, along with many other megafauna.[18]

Low genetic diversity

[edit]
Low genetic diversity could have hastened Arctodus' extinction.

Arctodus simus had a very low level of genetic diversity from most sampled specimens, albeit a sample with a Beringian and temporal bias (<44,000 BP). A loss and/or replacement of mitochondrial DNA lineages before the Last Glacial Maximum, and decrease in population size from a previously genetically diverse population, has been noted in a variety of Eurasian and American Late Pleistocene megafauna.[92][243] That the individual from Sheriden Cave, Ohio was very closely related to Beringian specimens may further support this idea, as these populations had possibly been isolated from before the Last Glacial Maximum (tens of thousands of years).[92]

A lack of genetic diversity has been attributed to a reduced ability to adapt to environmental conditions. Small population sizes may be characteristic of tremarctine bears- the spectacled bear, while having low levels of genetic diversity, has no signs of a recent genetic bottleneck. However, brown bears had diverse, sympatric source populations in Eurasia, allowing for repopulations/reinvasions into the Americas. If Arctodus simus experienced genetic bottlenecks or local extinctions prior to the Last Glacial Maximum, Arctodus would have been unable to supplement their reduced genetic diversity with new migrants like the brown bear could, making them vulnerable to extinction.[92]

Last dates

[edit]

The youngest date for Arctodus simus is circa 12,700 BP from Friesenhahn Cave, Texas, calibrated from 10,814 ± 55 radiocarbon years (14C BP). However, this date should be viewed with caution, as analyses suggest the collagen protein was degraded. A vertebra from Bonner Springs, Kansas, was dated to ca. 12,800 BP (based on 10,921 ± 50 radiocarbon years) from well preserved collagen. However, another radiocarbon date from a different laboratory on the same vertebra widens the possible age of the vertebra to between 9,510 and 11,021 14C BP (at 2σ). Nevertheless, a specimen from Huntington Dam, Utah was also dated to ca. 12,800 BP from two radiocarbon dates (10,870 ± 75 & 10,976 ± 40 14C BP) and is therefore considered reliable.[58][241]

History of research

[edit]

"Super predator" hypothesis

[edit]
Skeletal reconstruction of Arctodus simus at the Royal Ontario Museum, Toronto.

One past proposal envisaged A. simus as a brutish predator that overwhelmed very large but slow megafauna with its great physical strength.[74] However, despite being very large, its limbs were too gracile for such an attack strategy,[74][76][55] significantly more gracile so than Arctotherium angustidens at that.[41]

Due to their long legs, an alternative hypothesis suggested by Björn Kurtén is that it may have hunted by running down Pleistocene herbivores such as wild horses and saiga antelopes, an idea that at one time earned it the name "running bear".[46][47][130] However, during pursuit of speedy game animals, the bear's sheer physical mass, inflexible spine and plantigrade gait would be a handicap; modern brown bears can run at the same speed but quickly tire and cannot keep up a chase for long. Correspondingly, although a 700 kg (1,500 lb) Arctodus may have been able to reach a maximum speed of 51 kilometres per hour (32 mph), all modern bears have maximum speeds significantly lower than mass-based calculations for speed. As a result, paleontologist Paul Matheus suggests that Arctodus' top speed was 40–45 km/h (25–28 mph). Arctodus skeletons do not articulate in a way that would have allowed for quick turns – an ability required of any predator that survives by chasing down agile prey.[42][49][74] Proportionally taller legs, a short trunk, proximally elongated limbs, a stride which had little to no unsupported intervals, small and laterally-orientated eyes, and proportionally short canines ill-suited for spinal and tracheal attacks further complicated ambush hunting as a lifestyle for Arctodus.[28][49][73]

Furthermore, the lack of definitive predatory adaptions (such as the absence of laterally compressed canines, and carnassials built for crushing and grinding rather than shearing meat) puts doubt to any species-wide hyper-carnivorous interpretations of Arctodus.[47][78][49][71] The anatomical requirements for a large, cursorial, hyper-carnivorous bear are present in Huracan and Agriotherium, but not Arctodus.[73][244] Adaptations for predatory behavior are highly divergent in ursids versus other carnivorans, with features such as a short rostrum and long carnassials not being indicative of a predatory lifestyle in Arctodus.[71] Although the only living hyper-carnivorous ursid, the polar bear, also lacks carnassial shears, the species' specialization on small prey and reliance on blubber (rather than coarser flesh) invalidates this comparison with Arctodus.[28][49][71] However, both Arctodus simus and polar bears may have had similar overall limb proportions.[77] Regardless, carnivory was likely limited to the regular scavenging of carcasses and opportunistic hunting, as is the case with the modern brown bear.[46][47][49]

Specialist kleptoparasite vs Omnivore

[edit]
Mastodon arm bone from the Snowmastodon site with predator damage at the Denver Museum of Nature & Science in Denver, Colorado.

The idea that Arctodus was an obligate kleptoparasite was most notably proposed by Paul Matheus.[42] Under this model, A. simus was ill-equipped to be an active predator, having evolved as a specialized scavenger adapted to cover an extremely large home range in order to seek out broadly and unevenly distributed mega-mammal carcasses.[49] There would have been additional selective pressure for increased body size, so that Arctodus could procure and defend carcasses from other large carnivores, some of which were gregarious, or chase them from their kills and steal their food.[74] Matheus calculated that with a hyper-carnivorous diet, a 700 kg (1,500 lb) Beringian Arctodus would need to consume ~5,853 kilograms (12,904 lb) of meat per year- the equivalent of 12 bison, 44.6 horses, or 2 woolly mammoths (adjusted for the non-edible portions of the body). Therefore, Arctodus would have had to obtain 100 kg (220 lb) of flesh/edible carrion every 6.25 days (16 kg (35.3 lb) per day).[42][72][245]

Furthermore, the short rostrum, resulting in increased out-forces of the jaw-closing muscles (temporalis and masseter), may have been an adaptation for cracking bones with their broad carnassials. Such use of the P4 and m1 teeth is supported by the heavy wear on these teeth in old individuals of Arctodus simus and Agriotherium (another giant bear).[49] Additionally, strengthened tooth enamel in Arctodus may have evolved to crack bone.[70] Moreover, at least in Beringia, the conservative growth strategies, long lives and low natural mortality rates of horses and mammoths should have provided somewhat evenly distributed carcasses throughout the year (unlike ruminants such as bison, whose mortality peaks in late winter to early spring).[72] Finally, that Arctodus and the cave hyena did not spread into Siberia and North America respectively suggests some form of competitive exclusion was at play.[65]

Rebuttal

[edit]
Clues from Arctodus' dentition, such as the absence of molar damage associated with processing bone, dental cavities, and the lack of specialisation in the canines, discourages a hyper-carnivorous interpretation of Arctodus.

The kleptoparasite hypothesis has been repeatedly challenged. The short, broad rostrum of Arctodus is a characteristic also shared with the sun bear and the spectacled bear, which are both omnivorous.[47] Specialized scavengers like hyenas show distinctive patterns of molar damage from cracking bones. Based on lack of "bone-cracking" wear in specimens from Rancho La Brea, researchers in 2013 concluded that Arctodus simus was not a specialized scavenger. Of living bears, this population of A. simus showed the most similar tooth wear patterns to its closest living relative, the spectacled bear, which can have a highly varied diet ranging from omnivory to almost pure herbivory.[28][23]

Additionally, severe tooth crown fractures and alveolar infections were found in the South American giant short-faced bear (Arctotherium angustidens). These were interpreted as evidence of feeding on hard materials (e.g. bones), which could tentatively indicate for these bears the regular scavenging of ungulate carcasses obtained through kleptoparasitism. However, such dental pathologies were not observed in various specimens of A. simus, other than the strong wear facets of old individuals.[47] Instead, recovered dental damage (incisor wear, dental calculus & cavities) is herbivorous in origin.[57][87][18] Moreover, researchers in 2015 reviewing links between canine breakage, microwear texture patterns and carnivorans from La Brea found that A. simus consumed foods softer yet tougher than black bears and polar bears, avoided hard/brittle foods such as bone, and reaffirmed affinities between A. simus and modern, largely herbivorous spectacled bears.[95] In addition to hyenas, many other fauna did not cross the Rancholabrean Beringian gap, such as the American badger, Bootherium and the woolly rhino).[246][247][248]

Furthermore, the relative lack of Arctodus remains at predator traps such as the La Brea Tar Pits, suggests that Arctodus did not regularly compete for carcasses.[87] Although La Brea has produced more Arctodus simus specimens than any other site, Arctodus represents only 1% of all carnivorans in the pits.[95] While more abundant than brown bears and black bears, Arctodus was calculated to its baseline continental abundance, contrasting with the overabundance of other large carnivorans.[249] A similar rate (~0.9%) of relative abundance was calculated for Arctodus compared to other megafauna at the Natural Trap Cave in Wyoming by 1993.[250] Additionally, isotope analyses of Beringian Arctodus specimens suggest that Arctodus had a low consumption rate of horses and mammoths in Beringia, despite those species making up ~50% of the available biomass in Beringia.[100] Further evidence comes from the evolution of brain size relative to body size- bears with high caloric diets and which do not exhibit dormancy showed a weak but significant correlation with bigger relative brain size. Arctodus simus plotted in between the likely hypercarnivorous Cephalogale, and the almost exclusively herbivorous Eurasian cave bear and Indarctos, suggesting omnivory.[251]

See also

[edit]

References

[edit]
  1. ^ a b c d e f g h i "Arctodus pristinus". Florida Museum. 2017-03-30. Retrieved 2022-02-21.
  2. ^ a b c d e f g h i j k l m n o p q r Emslie, Steven D. (1995). "The fossil record of Arctodus pristinus (Ursidae: Tremarctinae) in Florida" (PDF). Bulletin of the Florida Museum of Natural History. 37 (15): 501–514. doi:10.58782/flmnh.hduf9651. S2CID 168164209.
  3. ^ "South Carolina Fossils". Nature. 20 (510): 354–355. 1879-08-01. Bibcode:1879Natur..20..354.. doi:10.1038/020354a0. ISSN 1476-4687. S2CID 4034608.
  4. ^ a b Cope E. D. (1879). "The cave bear of California". American Naturalist. 13: 791.
  5. ^ a b c Feranec, Robert S. (November 2009). "Implications of Radiocarbon Dates from Potter Creek Cave, Shasta County, California, USA". Radiocarbon. 51 (3): 931–936. Bibcode:2009Radcb..51..931F. doi:10.1017/S0033822200034007. S2CID 131722109.
  6. ^ a b Merriam, John C.; Stock, Chester (1925), Relationships and Structure of the Short-Faced Bear, Arctotherium, from the Pleistocene of California, Washington, DC: Carnegie institution of Washington, pp. 1–25, retrieved 2022-05-06
  7. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag Richards, Ronald L.; Churcher, C.S.; Turnbull, William D. (1996-12-31), "Distribution and size variation in North American Short-faced bears, Arctodus simus", Palaeoecology and Palaeoenvironments of Late Cenozoic Mammals, University of Toronto Press, pp. 191–246, doi:10.3138/9781487574154-012, ISBN 978-1-4875-7415-4, retrieved 2023-11-15
  8. ^ "Arctodus". www.utep.edu. Retrieved 2022-05-05.
  9. ^ Spamer, Earle E.; Daeschler, Edward; Philadelphia, Academy of Natural Sciences of; Vostreys-Shapiro, L. Gay (1995). A Study of Fossil Vertebrate Types in the Academy of Natural Sciences of Philadelphia: Taxonomic, Systematic, and Historical Perspectives. Academy of Natural Sciences. ISBN 978-0-910006-51-4.
  10. ^ Hay, Oliver Perry (1901). Bibliography and Catalogue of the Fossil Vertebrata of North America. U.S. Government Printing Office.
  11. ^ Kurtén, Björn (June 1, 1963). "Fossil Bears from Texas" (PDF). The Pearce-Sellards Series. 1 – via Texas Memorial Museum, University of Texas.
  12. ^ a b Ferrusquía-Villafranca, Ismael; Arroyo-Cabrales, Joaquín; Martínez-Hernández, Enrique; Gama-Castro, Jorge; Ruiz-González, José; Polaco, Oscar J.; Johnson, Eileen (2010-04-15). "Pleistocene mammals of Mexico: A critical review of regional chronofaunas, climate change response and biogeographic provinciality". Quaternary International. Faunal Dynamics and Extinction in the Quaternary: Studies in Honor of Ernest L. Lundelius, Jr. 217 (1): 53–104. Bibcode:2010QuInt.217...53F. doi:10.1016/j.quaint.2009.11.036. ISSN 1040-6182.
  13. ^ Arroyo-Cabrales, Joaquín; Polaco, Oscar J.; Johnson, Eileen; Ferrusquía-Villafranca, Ismael (2010-02-01). "A perspective on mammal biodiversity and zoogeography in the Late Pleistocene of México". Quaternary International. Quaternary Changes of Mammalian Communities Across and Between Continents. 212 (2): 187–197. Bibcode:2010QuInt.212..187A. doi:10.1016/j.quaint.2009.05.012. ISSN 1040-6182.
  14. ^ Schubert, Blaine W.; Chatters, James C.; Arroyo-Cabrales, Joaquin; Samuels, Joshua X.; Soibelzon, Leopoldo H.; Prevosti, Francisco J.; Widga, Christopher; Nava, Alberto; Rissolo, Dominique; Erreguerena, Pilar Luna (May 2019). "Yucatán carnivorans shed light on the Great American Biotic Interchange". Biology Letters. 15 (5): 20190148. doi:10.1098/rsbl.2019.0148. PMC 6548739. PMID 31039726.
  15. ^ a b c McLellan, Bruce; Reiner, David C. (1994). "A Review of bear evolution" (PDF). Int. Conf. Bear Res. And Manage. 9 (1): 85–96. doi:10.2307/3872687. JSTOR 3872687. Archived (PDF) from the original on 2022-10-09.
  16. ^ "Big Pine Citizen 2 March 1918 — California Digital Newspaper Collection". cdnc.ucr.edu. Retrieved 2024-07-18.
  17. ^ a b c d e f g h i j k Pedersen, Mikkel Winther; De Sanctis, Bianca; Saremi, Nedda F.; Sikora, Martin; Puckett, Emily E.; Gu, Zhenquan; Moon, Katherine L.; Kapp, Joshua D.; Vinner, Lasse; Vardanyan, Zaruhi; Ardelean, Ciprian F. (2021-06-21). "Environmental genomics of Late Pleistocene black bears and giant short-faced bears". Current Biology. 31 (12): 2728–2736.e8. Bibcode:2021CBio...31E2728P. doi:10.1016/j.cub.2021.04.027. hdl:10037/22808. PMID 33878301. S2CID 233303447.
  18. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab Steffen, Martina L.; Fulton, Tara L. (2018-02-01). "On the association of giant short-faced bear (Arctodus simus) and brown bear (Ursus arctos) in late Pleistocene North America". Geobios. 51 (1): 61–74. Bibcode:2018Geobi..51...61S. doi:10.1016/j.geobios.2017.12.001.
  19. ^ Soibelzon, Leopoldo H.; Romero, M.R. Aguilar (2008-10-14). "A Blancan (Pliocene) short-faced bear from El Salvador and its implications for Tremarctines in South America". Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen. 250 (1): 1–8. doi:10.1127/0077-7749/2008/0250-0001.
  20. ^ a b c d e f g h i j k l m n o p q r Schubert, Blaine; Hulbert, Richard; MacFadden, Bruce; Searle, Michael; Searle, Seina (2010-01-01). "Giant Short-faced Bears (Arctodus simus) in Pleistocene Florida USA, a Substantial Range Extension". Journal of Paleontology. 84 (1): 79–87. Bibcode:2010JPal...84...79S. doi:10.1666/09-113.1. S2CID 131532424.
  21. ^ a b c d Mitchell, Kieren J.; Bray, Sarah C.; Bover, Pere; Soibelzon, Leopoldo; Schubert, Blaine W.; Prevosti, Francisco; Prieto, Alfredo; Martin, Fabiana; Austin, Jeremy J.; Cooper, Alan (2016-04-30). "Ancient mitochondrial DNA reveals convergent evolution of giant short-faced bears (Tremarctinae) in North and South America". Biology Letters. 12 (4): 20160062. doi:10.1098/rsbl.2016.0062. PMC 4881349. PMID 27095265.
  22. ^ Krause, Johannes; Unger, Tina; Noçon, Aline; Malaspinas, Anna-Sapfo; Kolokotronis, Sergios-Orestis; Stiller, Mathias; Soibelzon, Leopoldo; Spriggs, Helen; Dear, Paul H; Briggs, Adrian W; Bray, Sarah CE; O'Brien, Stephen J; Rabeder, Gernot; Matheus, Paul; Cooper, Alan (December 2008). "Mitochondrial genomes reveal an explosive radiation of extinct and extant bears near the Miocene-Pliocene boundary". BMC Evolutionary Biology. 8 (1): 220. Bibcode:2008BMCEE...8..220K. doi:10.1186/1471-2148-8-220. ISSN 1471-2148. PMC 2518930. PMID 18662376.
  23. ^ a b c d e f g h i j Donohue, Shelly L.; DeSantis, Larisa R. G.; Schubert, Blaine W.; Ungar, Peter S. (30 October 2013). "Was the giant short-faced bear a hyper-scavenger? A new approach to the dietary study of ursids using dental microwear textures". PLOS ONE. 8 (10): e77531. Bibcode:2013PLoSO...877531D. doi:10.1371/journal.pone.0077531. PMC 3813673. PMID 24204860.
  24. ^ Brown, Gary (1996). Great Bear Almanac. Lyons & Burford. p. 340. ISBN 978-1-55821-474-3.
  25. ^ a b Russell, Dale A.; Rich, Fredrick J.; Schneider, Vincent; Lynch-Stieglitz, Jean (May 2009). "A warm thermal enclave in the Late Pleistocene of the South-eastern United States". Biological Reviews. 84 (2): 173–202. doi:10.1111/j.1469-185X.2008.00069.x. PMID 19391200. S2CID 9609391.
  26. ^ Morgan, Gary S. (2005). "The Great American Biotic Interchange in Florida" (PDF). Bulletin of the Florida Museum of Natural History. 45 (4): 271–311. doi:10.58782/flmnh.pkqn7297.
  27. ^ a b c d Bell, Christopher; Lundelius, Ernest L.; Barnosky, Anthony D.; Zarzewski, Richard J.; Graham, Russell; Lindsay, Everett H.; Ruez, Dennis R.; Semken, Holmes A.; Webb, S. David (2004-04-21). "Chapter 7: The Blancan, Irvingtonian, and Rancholabrean Mammal Ages". In Woodburne, Michael O. (ed.). Late Cretaceous and Cenozoic Mammals of North America. Columbia University Press. doi:10.7312/wood13040. ISBN 978-0-231-50378-5.
  28. ^ a b c d e f g h i j k l m n o p q Emslie, Steven D.; Czaplewski, Nicholas J. (1985-11-15). "A new record of giant short-faced bear, Arctodus simus, from western North America with a re-evaluation of its paleobiology". Contributions in Science. 371: 1–12. doi:10.5962/p.226835. S2CID 133986793.
  29. ^ a b c Martin, Larry; Neuner, A. (1978-01-01). "The End of the Pleistocene in North America". Transactions of the Nebraska Academy of Sciences and Affiliated Societies.
  30. ^ a b c d e f g Trayler, Robin B.; Dundas, Robert G.; Fox-Dobbs, Kena; Van De Water, Peter K. (2015-11-01). "Inland California during the Pleistocene—Megafaunal stable isotope records reveal new paleoecological and paleoenvironmental insights". Palaeogeography, Palaeoclimatology, Palaeoecology. 437: 132–140. Bibcode:2015PPP...437..132T. doi:10.1016/j.palaeo.2015.07.034. ISSN 0031-0182.
  31. ^ a b c d e f g Pérez-Crespo, Víctor Adrián; Arroyo-Cabrales, Joaquín; Morales-Puente, Pedro; Cienfuegos-Alvarado, Edith; Otero, Francisco J. (March 2018). "Diet and habitat of mesomammals and megamammals from Cedral, San Luis Potosí, México". Geological Magazine. 155 (3): 674–684. Bibcode:2018GeoM..155..674P. doi:10.1017/S0016756816000935. S2CID 132502543.
  32. ^ a b Harris, Arthur H. (November 1985). "Preliminary report on the vertebrate fauna of U-Bar Gave, Hidalgo County, New Mexico" (PDF). New Mexico Geology. 7 (4): 74–84. doi:10.58799/NMG-v7n4.74. S2CID 237056633.
  33. ^ a b c d e f g h i j k Esker, Donald; Wilkins, William; Agenbroad, Larry (2010-08-13). "Esker, Wilkins, and Agenbroad—Multivariate Analysis Of Ursids: A multivariate analysis of the ecology of North American Pleistocene bears, with a focus on Arctodus simus". ResearchGate.
  34. ^ Akersten, William A. (1996-12-31), "Diversity bottlenecks, oddball survivors, and negative keys", Palaeoecology and Palaeoenvironments of Late Cenozoic Mammals, University of Toronto Press, pp. 1–15, doi:10.3138/9781487574154-004, ISBN 978-1-4875-7415-4, retrieved 2024-01-23
  35. ^ Phillips, George Edward (6 August 2006). "Paleofaunistics of Nonmammalian Vertebrates from the Late Pleistocene of the Mississippi-Alabama Black Prairie". North Carolina State University (Masters) – via North Carolina State University Library.
  36. ^ a b c d e f g Scott, Eric; Cox, Shelley M. (May 24, 1993). "Arctodus simus (Cope, 1879) from Riverside County, California" (PDF). PaleoBios. 15 (2): 27–36.
  37. ^ a b c Hill, Christopher L.; Wilson, Mike C. (2000). "The Doeden Local Fauna (Illinoian/Sangamonian?), Eastern Montana". Unknown: 140–142 – via ResearchGate.
  38. ^ a b c d e f g h Kurtén, Björn (1967). Pleistocene Bears of North America: Genus Arctodus, short-faced bears. Societas pro Fauna et Flora Fennica.
  39. ^ a b c Van Valkenburgh, Blaire; Hayward, Matthew W.; Ripple, William J.; Meloro, Carlo; Roth, V. Louise (2016-01-26). "The impact of large terrestrial carnivores on Pleistocene ecosystems". Proceedings of the National Academy of Sciences. 113 (4): 862–867. Bibcode:2016PNAS..113..862V. doi:10.1073/pnas.1502554112. ISSN 0027-8424. PMC 4743832. PMID 26504224.
  40. ^ a b c Fowler, Nicholas L.; Spady, Thomas J.; Wang, Guiming; Leopold, Bruce D.; Belant, Jerrold L. (October 2021). "Denning, metabolic suppression, and the realisation of ecological opportunities in Ursidae". Mammal Review. 51 (4): 465–481. doi:10.1111/mam.12246. S2CID 233847639.
  41. ^ a b c d Soibelzon, Leopoldo H.; Schubert, Blaine W. (2011). "The Largest Known Bear, Arctotherium Angustidens, from the Early Pleistocene Pampean Region of Argentina: With a Discussion of Size and Diet Trends in Bears". Journal of Paleontology. 85 (1): 69–75. doi:10.1666/10-037.1. hdl:11336/104215. JSTOR 23019499. S2CID 129585554.
  42. ^ a b c d e Nancy Sisinyak. "The Biggest Bear ... Ever". Alaska Fish and Wildlife News. Retrieved 2008-01-12.
  43. ^ a b Fisher, W. A. (2018-02-05). "How Big Was This Short-Faced Bear?". North American Bear Center. Retrieved 2023-11-02.
  44. ^ "Giant Short-faced Bear | Yukon Beringia Interpretive Centre". www.beringia.com. Retrieved 2023-12-01.
  45. ^ a b c d e Richards, Ronald L.; Neiburger, Ellis J.; Turnbull, William D. (1995). Giant short-faced bear (Arctodus simus yukonensis) remains from Fulton County, northern Indiana. Chicago, Ill.: Field Museum of Natural History.
  46. ^ a b c d e f g h Mattson, David J. (1998). "Diet and Morphology of Extant and Recently Extinct Northern Bears". Ursus. 10: 479–496. JSTOR 3873160.
  47. ^ a b c d e f g h i j k l m n o p q r s Figueirido; et al. (2010). "Demythologizing Arctodus simus, the 'short-faced' long-legged and predaceous bear that never was". Journal of Vertebrate Paleontology. 30 (1): 262–275. Bibcode:2010JVPal..30..262F. doi:10.1080/02724630903416027. hdl:10630/33066. S2CID 85649497.
  48. ^ a b Christiansen, Per (1999). "What size were Arctodus simus and Ursus spelaeus (Carnivora: Ursidae)?". Annales Zoologici Fennici. 36 (2): 93–102. JSTOR 23735739.
  49. ^ a b c d e f g h i j k l m n o p q r Sorkin, B. (January 2006). "Ecomorphology of the giant short-faced bears Agriotherium and Arctodus". Historical Biology. 18 (1): 1–20. Bibcode:2006HBio...18....1S. doi:10.1080/08912960500476366. S2CID 85301983.
  50. ^ a b Lambert, W. David; Holling, Crawford S. (1998-03-01). "Original Articles: Causes of Ecosystem Transformation at the End of the Pleistocene: Evidence from Mammal Body-Mass Distributions". Ecosystems. 1 (2): 157–175. Bibcode:1998Ecosy...1..157L. doi:10.1007/s100219900012. ISSN 1432-9840. S2CID 29456831.
  51. ^ a b c Kurten, B.; Anderson, Elaine (1974). "Association of Ursus arctos and Arctodus simus (Mammalia: Ursidae) in the late Pleistocene of Wyoming". Breviora. 426: 1––6. ISSN 0006-9698.
  52. ^ "The California grizzly bear | La Brea Tar Pits". tarpits.org. Retrieved 2022-06-22.
  53. ^ a b Nelson, Michael E.; Madsen, James H. (1983). "A Giant Short-Faced Bear (Arctodus simus) from the Pleistocene of Northern Utah". Transactions of the Kansas Academy of Science. 86 (1): 1–9. doi:10.2307/3628418. JSTOR 3628418.
  54. ^ a b c d e f Lucas, Spencer G.; Sullivan, Robert M. Vertebrate Paleontology in New Mexico: Bulletin 68. New Mexico Museum of Natural History and Science.
  55. ^ a b c d e f g h Paul, Matheus (2001). "Pleistocene carnivores and humans in eastern Beringia: did short-faced bears really keep people out of North America?". In Gerlach, S. Craig; Murray, Maribeth S. (eds.). People and Wildlife in Northern North America: Essays in honor of R. Dale Guthrie. BAR Publishing. pp. 79–101. doi:10.30861/9781841712369. ISBN 978-1-4073-5292-3.
  56. ^ a b c d e f Stark, Mike (2022). Chasing the Ghost Bear: On the Trail of America's Lost Super Beast. University of Nebraska Press. doi:10.2307/j.ctv2br108d. ISBN 978-1-4962-2902-1. JSTOR j.ctv2br108d. S2CID 247872305.
  57. ^ a b c d e f g h i Schubert, Blaine; Kaufmann, James (2003-08-01). "A partial short-faced bear skeleton from an Ozark Cave with comments on the paleobiology of the species". Journal of Cave and Karst Studies. 65.
  58. ^ a b c d Schubert, Blaine W. (2010-04-15). "Late Quaternary chronology and extinction of North American giant short-faced bears (Arctodus simus)". Quaternary International. Faunal Dynamics and Extinction in the Quaternary: Studies in Honor of Ernest L. Lundelius, Jr. 217 (1): 188–194. Bibcode:2010QuInt.217..188S. doi:10.1016/j.quaint.2009.11.010.
  59. ^ a b c d e Schubert, Blaine W.; Wallace, Steven C. (August 2009). "Late Pleistocene giant short-faced bears, mammoths, and large carcass scavenging in the Saltville Valley of Virginia, USA". Boreas. 38 (3): 482–492. Bibcode:2009Borea..38..482S. doi:10.1111/j.1502-3885.2009.00090.x. S2CID 129612660.
  60. ^ Goswami, Anjali; Milne, Nick; Wroe, Stephen (2011-06-22). "Biting through constraints: cranial morphology, disparity and convergence across living and fossil carnivorous mammals". Proceedings of the Royal Society B: Biological Sciences. 278 (1713): 1831–1839. doi:10.1098/rspb.2010.2031. ISSN 0962-8452. PMC 3097826. PMID 21106595.
  61. ^ a b c Matheus, Paul E. (1995-11-01). "Diet and Co-ecology of Pleistocene Short-Faced Bears and Brown Bears in Eastern Beringia". Quaternary Research. 44 (3): 447–453. Bibcode:1995QuRes..44..447M. doi:10.1006/qres.1995.1090. ISSN 0033-5894. S2CID 83542760.
  62. ^ a b c d e f g FIGUEIRIDO, BORJA; SOIBELZON, LEOPOLDO H. (2009-08-19). "Inferring palaeoecology in extinct tremarctine bears (Carnivora, Ursidae) using geometric morphometrics". Lethaia. 43 (2): 209–222. doi:10.1111/j.1502-3931.2009.00184.x.
  63. ^ a b c d Gillette, David D.; Madsen, David B. (1992-03-06). "The short-faced bear Arctodus simus from the late Quaternary in the Wasatch Mountains of central Utah". Journal of Vertebrate Paleontology. 12 (1): 107–112. Bibcode:1992JVPal..12..107G. doi:10.1080/02724634.1992.10011436.
  64. ^ a b c Slaughter, B. H.; Crook, W. W. Jr.; Harris, R. K.; Allen, D. C.; Seifert, M. (1962-01-01). The Hill-Shuler Local Faunas of the Upper Trinity River, Dallas and Denton Counties, Texas. Report Investigation. The University of Texas at Austin, Bureau of Economic Geology. doi:10.23867/ri0048d.
  65. ^ a b c d Baryshnikov, Gennady (1994). Agenbroad, Larry D.; Mead, Jim I. (eds.). The Hot Springs Mammoth Site: A Decade of Field and Laboratory Research in Paleontology, Geology and Paleoecology. The Mammoth Site of Hot Springs, South Dakota Inc. pp. Chapter 16.
  66. ^ Dickinson, Edwin; Elminowski, Erin E.; Flores, Deanna; Eldridge, Emma I.; Granatosky, Michael C.; Hartstone-Rose, Adam (October 2022). "A morphological analysis of carnivoran ossicles from Rancho La Brea". Journal of Morphology. 283 (10): 1337–1349. doi:10.1002/jmor.21506. ISSN 0362-2525. PMC 9826070. PMID 36041006.
  67. ^ a b Meloro, Carlo (2011-03-17). "Feeding habits of Plio-Pleistocene large carnivores as revealed by the mandibular geometry". Journal of Vertebrate Paleontology. 31 (2): 428–446. Bibcode:2011JVPal..31..428M. doi:10.1080/02724634.2011.550357. ISSN 0272-4634. S2CID 85255472.
  68. ^ a b Voorhies, M. R.; Corner, R. G. (1986). "Giant Bear Arctodus as a Potential Breaker and Flaker of Late Pleistocene Megafaunal Remains". Current Research in the Pleistocene. 3: 49–51.
  69. ^ a b Sanders, Albert E. (2002). Additions to the Pleistocene Mammal Faunas of South Carolina, North Carolina, and Georgia. American Philosophical Society. ISBN 978-0-87169-925-1.
  70. ^ a b Stefen, Clara (2001). "Enamel Structure of Arctoid Carnivora: Amphicyonidae, Ursidae, Procyonidae, and Mustelidae". Journal of Mammalogy. 82 (2): 450–462. doi:10.1644/1545-1542(2001)082<0450:ESOACA>2.0.CO;2. ISSN 0022-2372. JSTOR 1383726. S2CID 85871953.
  71. ^ a b c d e f Figueirido, B.; Palmqvist, P.; Pérez-Claros, J. A. (2008-12-22). "Ecomorphological correlates of craniodental variation in bears and paleobiological implications for extinct taxa: an approach based on geometric morphometrics". Journal of Zoology. 277 (1): 70–80. doi:10.1111/j.1469-7998.2008.00511.x. ISSN 0952-8369.
  72. ^ a b c d e f g Matheus, Paul Edward (1997). Paleoecology and ecomorphology of the giant short-faced bear in Eastern Beringia (PhD thesis).
  73. ^ a b c d e f g Jiangzuo, Qigao; Flynn, John J.; Wang, Shiqi; Hou, Sukuan; Deng, Tao (2023-03-14). "New Fossil Giant Panda Relatives (Ailuropodinae, Ursidae): A Basal Lineage of Gigantic Mio-Pliocene Cursorial Carnivores". American Museum Novitates (3996): 1–71. doi:10.1206/3996.1. ISSN 0003-0082. S2CID 257508340.
  74. ^ a b c d e f g h Matheus, Paul E. (2003). Locomotor adaptations and ecomorphology of short-faced bears (Arctodus simus) in eastern Beringia. Yukon Palaeontologist, Gov't. of Yukon. OCLC 243520303.
  75. ^ a b Churcher, C. S.; Morgan, A. V.; Carter, L. D. (2011-02-08). "Arctodus simus from the Alaskan Arctic Slope". Canadian Journal of Earth Sciences. 30 (5): 1007–1013. doi:10.1139/e93-084.
  76. ^ a b c Lynch, Eric Randally (2012-08-06). Cursorial Adaptations in the Forelimb of the Giant Short-Faced Bear, Arctodus simus, Revealed by Traditional and 3D Landmark Morphometrics. East Tennessee State University. OCLC 818344518.
  77. ^ a b c Samuels, Joshua X.; Meachen, Julie A.; Sakai, Stacey A. (13 September 2012). "Postcranial morphology and the locomotor habits of living and extinct carnivorans". Journal of Morphology. 274 (2): 121–146. doi:10.1002/jmor.20077. ISSN 0362-2525. PMID 22972188.
  78. ^ a b c Meloro, Carlo; de Oliveira, Alessandro Marques (2019-03-01). "Elbow Joint Geometry in Bears (Ursidae, Carnivora): a Tool to Infer Paleobiology and Functional Adaptations of Quaternary Fossils" (PDF). Journal of Mammalian Evolution. 26 (1): 133–146. doi:10.1007/s10914-017-9413-x. S2CID 25839635.
  79. ^ Weems, Robert E. (2018). "An Early Pleistocene (Early Irvingtonian) Footprint Fauna from the Bacons Castle Formation, Westmoreland Formation, Virginia". New Mexico Museum of Natural History and Science Bulletin. 79: 731–748 – via ResearchGate.
  80. ^ Stucchi, Marcelo; Salas-Gismondi, Rodolfo; Baby, Patrice; Guyot, Jean-Loup; Shockey, Bruce J. (2009). "A 6,000+ year-old specimen of a spectacled bear from an Andean cave in Peru". Ursus. 20: 63–68. doi:10.2192/08GR017R1.1. S2CID 86731722.
  81. ^ Packard, E.L.; Allison, I.S.; Cressman, L.S. "Mammalian Tracks in the Late Pliocene or Early Pleistocene Beds of Lake County Oregon" (PDF). Oregon Geology. Retrieved June 11, 2017.
  82. ^ Gentry, Andrew; Franco, Christopher Michael; Bustos, David (September 2011). "Mammalian Ichnofauna from the Upper-Pleistocene deposits of White Sands National Monument, Otero County, New Mexico". Geoscientists-in-the Parks, National Park Service, Denver, Colorado. – via ResearchGate.
  83. ^ Nadeau, Andy J.; Allen, Kathy; Benck, Kevin; Davis, Anna M.; Hutchins, Hannah; Gardner, Sarah; Amberg, Shannon; Robertson, Andrew (September 2017). "White Sands National Monument Natural Resource Condition Assessment" (PDF). Natural Resource Report NPS/WHSA/NRR—2017/1508: 276–277 – via National Park Service, Fort Collins, Colorado.
  84. ^ a b Lucas, Spencer G.; Spielmann, Justin A.; Lockley, Martin G. (2007). "Cenozoic Vertebrate Tracks and Traces". New Mexico Museum of Natural History and Science Bulletin. 42.
  85. ^ Rovey II, Charles W.; Forir, Matt; Balco, Greg; Gaunt, David (2010-01-01). "Geomorphology and Paleontology of Riverbluff Cave, Springfield, Missouri". In Evans, Kevin R.; Aber, James S. (eds.). From Precambrian Rift Volcanoes to the Mississippian Shelf Margin: Geological Field Excursions in the Ozark Mountains (Field Guide 17 ed.). Geological Society of America. pp. 31–32. ISBN 978-0-8137-0017-5.
  86. ^ a b Salesa, M. J.; Siliceo, G.; Antón, M.; Abella, J.; Montoya, P.; Morales, J. (2006-12-30). "Anatomy of the "false thumb" of Tremarctos ornatus (Carnivora, Ursidae, Tremarctinae): Phylogenetic and functional implications". Estudios Geológicos. 62 (1): 389–394. doi:10.3989/egeol.0662133. hdl:10261/22444. ISSN 1988-3250.
  87. ^ a b c d e f g h i j k l m Figueirido, Borja; Perez, Alejandro; Schubert, Blaine; Serrano, Francisco; Farrell, Aisling; Pastor, Francisco; Neves, Aline; Romero, Alejandro (2017-12-19). "Dental caries in the fossil record: A window to the evolution of dietary plasticity in an extinct bear". Scientific Reports. 7 (1): 17813. Bibcode:2017NatSR...717813F. doi:10.1038/s41598-017-18116-0. PMC 5736623. PMID 29259277.
  88. ^ Rothschild, Bruce M.; Martin, Larry D. (2006). Skeletal Impact of Disease: Bulletin 33. New Mexico Museum of Natural History and Science.
  89. ^ Rothschild, Bruce M. (13 October 1988). "Scientific Correspondence" (PDF). Nature. 335 (Existence of syphilis in a Pleistocene bear): 595. doi:10.1038/335595a0. PMID 3050529. S2CID 4280184.
  90. ^ Pinto, A. C.; Etxebarría, F. (2001). "Description of pathological conditions in the skeleton of an adult male brown bear Ursus arctos from the Cantabrian range of mountains (Reserva Nacional de Caza de Riaño, León) Coruña" (PDF). Cadernos Lab. Xeolóxico de Laxe. 2001: 471. ISSN 0213-4497.
  91. ^ a b c d e f g Steffen, Martina L.; Harington, C. R. Harington (2010-07-23). "Giant short-faced bear (Arctodus simus) from late Wisconsinan deposits at Cowichan Head, Vancouver Island, British Columbia". Canadian Journal of Earth Sciences. 47 (8): 1029–1036. Bibcode:2010CaJES..47.1029S. doi:10.1139/E10-018.
  92. ^ a b c d e f Bray, Sarah C. E. (September 2010). Mitochondrial DNA Analysis of the Evolution and Genetic Diversity of Ancient and Extinct Bears (PDF) (Thesis). School of Environmental and Earth Sciences, University of Adelaide. pp. 214 (230).
  93. ^ a b c d e f g h i Mychajliw, Alexis M.; Rick, Torben C.; Dagtas, Nihan D.; Erlandson, Jon M.; Culleton, Brendan J.; Kennett, Douglas J.; Buckley, Michael; Hofman, Courtney A. (2020-09-16). "Biogeographic problem-solving reveals the Late Pleistocene translocation of a short-faced bear to the California Channel Islands". Scientific Reports. 10 (1): 15172. doi:10.1038/s41598-020-71572-z. PMC 7494929. PMID 32938967.
  94. ^ a b Jones, D. Brent; Desantis, Larisa R. G. (2016-06-29). "Dietary Ecology of the Extinct Cave Bear: Evidence of Omnivory as Inferred from Dental Microwear Textures". Acta Palaeontologica Polonica. 61 (4): 735–741. doi:10.4202/app.00253.2016. ISSN 0567-7920. S2CID 55803102.
  95. ^ a b c d DeSantis, Larisa; Schubert, Blaine; Schmitt-Linville, Elizabeth; Ungar, Peter; Donohue, Shelly; Haupt, Ryan (2015-01-01). "Dental Microwear Textures of Carnivorans from the La Brea Tar Pits, California, and Potential Extinction Implications". La Brea and Beyond: The Paleontology of Asphalt-Preserved Biotas: 37–52.
  96. ^ Carbone, Chris; Teacher, Amber; Rowcliffe, J. Marcus (2007-01-16). "The Costs of Carnivory". PLOS Biology. 5 (2): e22. doi:10.1371/journal.pbio.0050022. ISSN 1545-7885. PMC 1769424. PMID 17227145.
  97. ^ Smith, Felisa A.; Boyer, Alison G.; Brown, James H.; Costa, Daniel P.; Dayan, Tamar; Ernest, S. K. Morgan; Evans, Alistair R.; Fortelius, Mikael; Gittleman, John L.; Hamilton, Marcus J.; Harding, Larisa E.; Lintulaakso, Kari; Lyons, S. Kathleen; McCain, Christy; Okie, Jordan G. (2010-11-26). "The Evolution of Maximum Body Size of Terrestrial Mammals". Science. 330 (6008): 1216–1219. Bibcode:2010Sci...330.1216S. doi:10.1126/science.1194830. ISSN 0036-8075. PMID 21109666. S2CID 17272200.
  98. ^ Lauriol, Bernard; Gotthardt, Ruth (2016). Leduc, Heather (ed.). The Ni'iinlii Njik Caves, Northern Yukon (PDF). Government of Yukon. ISBN 978-1-55362-752-4.
  99. ^ Soibelzon, Leopoldo H.; Grinspan, Gustavo A.; Bocherens, Hervé; Acosta, Walter G.; Jones, Washington; Blanco, Ernesto R.; Prevosti, Francisco (November 2014). "South American giant short-faced bear (Arctotherium angustidens) diet: evidence from pathology, morphology, stable isotopes, and biomechanics". Journal of Paleontology. 88 (6): 1240–1250. Bibcode:2014JPal...88.1240S. doi:10.1666/13-143. hdl:11336/34149. ISSN 0022-3360. S2CID 54869873.
  100. ^ a b c d e f g h i j k l m n Bocherens, Hervé (2015-06-01). "Isotopic tracking of large carnivore palaeoecology in the mammoth steppe". Quaternary Science Reviews. 117: 42–71. Bibcode:2015QSRv..117...42B. doi:10.1016/j.quascirev.2015.03.018. ISSN 0277-3791.
  101. ^ a b c Smith, Felisa A.; Elliott Smith, Emma A.; Villaseñor, Amelia; Tomé, Catalina P.; Lyons, S. Kathleen; Newsome, Seth D. (2022-09-27). "Late Pleistocene megafauna extinction leads to missing pieces of ecological space in a North American mammal community". Proceedings of the National Academy of Sciences. 119 (39): e2115015119. Bibcode:2022PNAS..11915015S. doi:10.1073/pnas.2115015119. ISSN 0027-8424. PMC 9522422. PMID 36122233.
  102. ^ a b c d e f g h i j Kubiak, Cara; Grimes, Vaughan; Van Biesen, Geert; Keddie, Grant; Buckley, Mike; Macdonald, Reba; Richards, M. P. (2022-06-27). "Dietary niche separation of three Late Pleistocene bear species from Vancouver Island, on the Pacific Northwest Coast of North America". Journal of Quaternary Science. 38: 8–20. doi:10.1002/jqs.3451. ISSN 0267-8179. S2CID 250134103.
  103. ^ a b c d e Fox-Dobbs, Kena; Leonard, Jennifer A.; Koch, Paul L. (2008-04-24). "Pleistocene megafauna from eastern Beringia: Paleoecological and paleoenvironmental interpretations of stable carbon and nitrogen isotope and radiocarbon records". Palaeogeography, Palaeoclimatology, Palaeoecology. 261 (1): 30–46. Bibcode:2008PPP...261...30F. doi:10.1016/j.palaeo.2007.12.011. ISSN 0031-0182.
  104. ^ Daeschler, Edward B. (1996-12-31), "Selective mortality of mastodons (Mammut americanum) from the Port Kennedy Cave (Pleistocene; lrvingtonian), Montgomery County, Pennsylvania", Palaeoecology and Palaeoenvironments of Late Cenozoic Mammals, University of Toronto Press, pp. 83–96, doi:10.3138/9781487574154-008, ISBN 978-1-4875-7415-4, retrieved 2024-01-23
  105. ^ a b "A Baby Mastodon Deathtrap (?)". Science. 2010-02-17. Archived from the original on June 9, 2022. Retrieved 2022-06-09.
  106. ^ Guthrie, R. Dale (1988). Mead, Jim I. (ed.). "Bone Litter from an Alaskan Pleistocene Carnivore Den" (PDF). Current Research in the Pleistocene. 5: 84–85.
  107. ^ Sattler, Robert A. (1997). "Large Mammals in Lower Rampart Cave 1, Alaska: Interspecific Utilization of an Eastern Beringian Cave". Geoarchaeology. 12 (6): 657–688. Bibcode:1997Gearc..12..657S. doi:10.1002/(SICI)1520-6548(199709)12:6<657::AID-GEA7>3.0.CO;2-Y.
  108. ^ a b c d e f g h i j k l Salis, Alexander T; Bray, Sarah C E; Lee, Michael S Y; Heiniger, Holly; Barnett, Ross; Burns, James A; Doronichev, Vladimir; Fedje, Daryl; Golovanova, Liubov; Harington, C Richard; Hockett, Bryan; Kosintsev, Pavel; Lai, Xulong; Mackie, Quentin; Vasiliev, Sergei; Weinstock, Jacobo; Yamaguchi, Nobuyuki; Meachen, Julie; Cooper, Alan; Mitchell, Kieren J (3 September 2020). "Lions and brown bears colonized North America in multiple synchronous waves of dispersal across the Bering Land Bridge". bioRxiv 10.1101/2020.09.03.279117.
  109. ^ a b c Redmond, Brian G.; Tankersley, Kenneth B. (10 February 2005). "Evidence of Early Paleoindian Bone Modification and Use at the Sheriden Cave Site (33WY252), Wyandot County, Ohio". American Antiquity. 70 (3): 503–526. doi:10.2307/40035311. ISSN 0002-7316. JSTOR 40035311. S2CID 162034505.
  110. ^ BOCHERENS, H; EMSLIE, S. D.; BILLIOU, D.; MARIOTTI, A. (1995). "Stables isotopes (13C, 15N) and paleodiet of the giant short-faced bear (Arctodus simus)". Stables Isotopes (13C, 15N) and Paleodiet of the Giant Short-faced Bear (Arctodus Simus). 320 (8): 779–784. ISSN 1251-8050.
  111. ^ Rawlence, Nicolas J.; Wood, Jamie R.; Bocherens, Herve; Rogers, Karyne M. (2016-06-15). "Dietary interpretations for extinct megafauna using coprolites, intestinal contents and stable isotopes: Complimentary or contradictory?". Quaternary Science Reviews. 142: 173–178. Bibcode:2016QSRv..142..173R. doi:10.1016/j.quascirev.2016.05.017. ISSN 0277-3791.
  112. ^ a b c Kohn, Matthew J.; McKay, Moriah P. (2012-04-01). "Paleoecology of late Pleistocene–Holocene faunas of eastern and central Wyoming, USA, with implications for LGM climate models". Palaeogeography, Palaeoclimatology, Palaeoecology. 326–328: 42–53. Bibcode:2012PPP...326...42K. doi:10.1016/j.palaeo.2012.01.037. ISSN 0031-0182.
  113. ^ Fisher, Daniel C.; Cherney, Michael D.; Newton, Cody; Rountrey, Adam N.; Calamari, Zachary T.; Stucky, Richard K.; Lucking, Carol; Petrie, Lesley (November 2014). "Taxonomic overview and tusk growth analyses of Ziegler Reservoir proboscideans". Quaternary Research. 82 (3): 518–532. Bibcode:2014QuRes..82..518F. doi:10.1016/j.yqres.2014.07.010. ISSN 0033-5894. S2CID 42376537.
  114. ^ a b Trayler, Robin Brendan (December 2012). "Stable Isotope Records of Inland California Megafauna- New Insights Into Pleistocene Paleoecology and Paleoenvironmental Conditions (Masters Thesis)". College of Science and Mathematics, California State University Fresno.
  115. ^ Lanoë, François B.; Reuther, Joshua D.; Holmes, Charles E.; Hodgins, Gregory W. L. (2017-11-01). "Human paleoecological integration in subarctic eastern Beringia". Quaternary Science Reviews. 175: 85–96. Bibcode:2017QSRv..175...85L. doi:10.1016/j.quascirev.2017.10.003. ISSN 0277-3791.
  116. ^ a b Daeschler, Edward B.; Spamer, Earl E.; Parris, David C. (1993). "Review and New Data on the Port Kennedy Local Fauna and Flora (Late Irvingtonian), Valley Forge National Historical Park, Montgomery County, Pennsylvania". The Mosasaur - Delaware Valley Paleontological Society. 5: 23–41 – via ResearchGate.
  117. ^ Soibelzon, Leopoldo H.; Pomi, Lucas H.; Tonni, Eduardo P.; Rodriguez, Sergio; Dondas, Alejandro (2009-09-01). "First report of a South American short-faced bears' den (Arctotherium angustidens): palaeobiological and palaeoecological implications". Alcheringa: An Australasian Journal of Palaeontology. 33 (3): 211–222. Bibcode:2009Alch...33..211S. doi:10.1080/03115510902844418. ISSN 0311-5518. S2CID 55636895.
  118. ^ a b Czaplewski, Nicholas; Rogers, Kyler; Russell, Clayton (2018-06-01). "Late pleistocene vertebrates from three-forks cave, Adair county, Oklahoma Ozark highland". Journal of Cave and Karst Studies. 80 (2): 1–16. doi:10.4311/2017PA0118.
  119. ^ a b Puckette, William L. (1976). "Notes on the occurrence of the short-faced bear (Arctodus) in Oklahoma". Proceedings of the Oklahoma Academy of Science. 56: 67–68. CiteSeerX 10.1.1.605.3584.
  120. ^ Grumet, Robert S. (September 2000). Bay, Plain, and Piedmont- A Landscape History of the Chesapeake Heartland from 1.3 Billion Years Ago to 2000. The Chesapeake Bay Heritage Context Project. pp. 16, 21, 167.
  121. ^ Morgan, Gary S.; Lucas, Spencer G. (2005). "Pleistocene vertebrate faunas in New Mexico from alluvial, fluvial, and lacustrine deposits". New Mexico Museum of Natural History and Science Bulletin. 28: 207.
  122. ^ a b c Albright, L. Barry; Sanders, Albert; Weems, Robert; Cicimurri, David; Knight, James (2020-01-24). "Cenozoic Vertebrate Biostratigraphy of South Carolina, USA, and Additions to the Fauna". Showcase of Faculty Scholarly & Creative Activity.
  123. ^ Dalquest, W. W.; Mooser, O. (1980-12-19). "Arctodus pristinus Leidy in the Pleistocene of Aguascalientes, Mexico". Journal of Mammalogy. 61 (4): 724–725. doi:10.2307/1380320. JSTOR 1380320.
  124. ^ White Jr., Richard S.; Morgan, Gary S. (2005). "Arizonan Blancan Vertebrate Faunas in Regional Perspective". Vertebrate Paleontology of Arizona, Mesa Southwest Museum Bulletin. 11.
  125. ^ Berta, Annalisa (1995). "Fossil carnivores from the Leisley Shell Pit, Hillsborough County, Florida" (PDF). Bulletin of the Florida Museum of Natural History. 37 Part II (14): 436–499.
  126. ^ Gould, G.C.; Quitmyer, Irvy (2005-01-01). "Titanis walleri: Bones of contention". Bulletin of the Florida Museum of Natural History. 45 (4): 201–229. doi:10.58782/flmnh.xumx1681.
  127. ^ MacFadden, Bruce; Labs-Hochstein, Joann; Hulbert, Richard; Baskin, Jon (2007-02-01). "Revised age of the late Neogene terror bird (Titanis) in North America during the Great American Interchange". Geology. 35 (2): 123. Bibcode:2007Geo....35..123M. doi:10.1130/G23186A.1.
  128. ^ a b Domínguez-Rodrigo, Manuel; Egeland, Charles P.; Cobo-Sánchez, Lucía; Baquedano, Enrique; Hulbert, Richard C. (2022-05-02). "Sabertooth carcass consumption behavior and the dynamics of Pleistocene large carnivoran guilds". Scientific Reports. 12 (1): 6045. Bibcode:2022NatSR..12.6045D. doi:10.1038/s41598-022-09480-7. ISSN 2045-2322. PMC 9061710. PMID 35501323.
  129. ^ Legge, A. J. (March 1991). "Where ends meat". Antiquity. 65 (246): 147–153. doi:10.1017/S0003598X00079424. ISSN 0003-598X. S2CID 163458417.
  130. ^ a b "The Giant Short-Faced Bear". North American Bear Center. 2018-03-02. Retrieved 2022-03-01.
  131. ^ "great short-faced bear fossil". www.backyardnature.net. Retrieved 2023-10-23.
  132. ^ a b Holliday, Vance; Surovell, Todd; Meltzer, David; Grayson, Donald; Boslough, Mark (2014-08-01). "The Younger Dryas impact hypothesis: A cosmic catastrophe". Journal of Quaternary Science. 29 (6): 515–530. Bibcode:2014JQS....29..515H. doi:10.1002/jqs.2724. S2CID 18644154.
  133. ^ a b c Faith, J. Tyler; Surovell, Todd A. (2009-12-08). "Synchronous extinction of North America's Pleistocene mammals". Proceedings of the National Academy of Sciences. 106 (49): 20641–20645. Bibcode:2009PNAS..10620641F. doi:10.1073/pnas.0908153106. ISSN 0027-8424. PMC 2791611. PMID 19934040.
  134. ^ Pichardo, Mario (2003). "Overview of Central Mexican Prehistory: Morphostratigraphy, Chronostratigraphy, Biostratigraphy". Anthropologischer Anzeiger. 61 (2): 141–174. doi:10.1127/anthranz/61/2003/141. ISSN 0003-5548. JSTOR 29542453. PMID 12872543.
  135. ^ "KGS--Guidebook 5--Wisconsinan Mammalian Faunas". www.kgs.ku.edu. Retrieved 2022-08-01.
  136. ^ Firby, Jean Brower (1968). Revision of the Middle Pleistocene Irvington Fauna of California. University of California.
  137. ^ III, Alois F. Pajak; Scott, Eric; Bell, Christopher J. (13 September 1996). "A review of the biostratigraphy of Pliocene and Pleistocene sediments in the Elsinore Fault Zone, Riverside County, California" (PDF). PaleoBios. 17 (2–4): 28–49.
  138. ^ "Elsinore Fault Zone". www.utep.edu. Retrieved 2024-07-22.
  139. ^ Dundas, Robert G.; Chatters, James C. (2013-01-01). "The mid-Irvingtonian Fairmead Landfill fossil site, Madera County Paleontology Collection, and Fossil Discovery Center of Madera County, California". In Keith Putirka (ed.). Geologic Excursions from Fresno, California, and the Central Valley: A Tour of California's Iconic Geology. Geological Society of America. pp. 63–78. doi:10.1130/2013.0032(04). ISBN 978-0-8137-0032-8.
  140. ^ "San Timoteo Badlands". www.utep.edu. Retrieved 2024-07-22.
  141. ^ Tar Pits Fossil Count (PDF). La Brea Tar Pits and Museum.
  142. ^ Carbone, Chris; Maddox, Tom; Funston, Paul J.; Mills, Michael G.L.; Grether, Gregory F.; Van Valkenburgh, Blaire (2009-02-23). "Parallels between playbacks and Pleistocene tar seeps suggest sociality in an extinct sabretooth cat, Smilodon". Biology Letters. 5 (1): 81–85. doi:10.1098/rsbl.2008.0526. ISSN 1744-9561. PMC 2657756. PMID 18957359.
  143. ^ Springer, Kathleen; Scott, Eric; Murray, Lyndon K.; Sagebiel, James (2009). Albright, L. B. III (ed.). "The Diamond Valley Lake local fauna: late Pleistocene vertebrates from inland southern California". Papers on Geology, Vertebrate Paleontology, and Biostratigraphy in Honor of Michael O. Woodburne.
  144. ^ a b c d e University of Geneva, Switzerland; Ray, N.; Adams, J.M. (2001). "A GIS-based Vegetation Map of the World at the Last Glacial Maximum (25,000-15,000 BP)". Internet Archaeology (11). doi:10.11141/ia.11.2.
  145. ^ a b Goebel, Ted; Hockett, Bryan; Adams, Kenneth D.; Rhode, David; Graf, Kelly (2011-10-15). "Climate, environment, and humans in North America's Great Basin during the Younger Dryas, 12,900–11,600 calendar years ago". Quaternary International. HUMANS AND YOUNGER DRYAS: DEAD END, SHORT DETOUR, OR OPEN ROAD TO THE HOLOCENE?. 242 (2): 479–501. Bibcode:2011QuInt.242..479G. doi:10.1016/j.quaint.2011.03.043. ISSN 1040-6182.
  146. ^ Long, C. A. (1971). "Significance of the Late Pleistocene fauna from the Little Box Elder Cave, Wyoming, to studies of zoogeography of recent mammals". Great Basin Naturalist. 31 (2) 11. S2CID 55933331.
  147. ^ Walker, Danny N. (1987). "Late Pleistocene/Holocene Environmental Changes in Wyoming: the Mammalian Record" (PDF). Office of the Wyoming State Archeologist.
  148. ^ Smith, Larry N.; Hill, Christopher L.; Reiten, Jon. "Quaternary and Late Tertiary of Montana: Climate, Glaciation, Stratigraphy, and Vertebrate Fossils" (PDF). Montana Bureau of Mines and Geology Publication 122. 1: Geologic History – via Montana Bureau of Mines and Geology.
  149. ^ Hill, Christopher L. (2006-01-01). "Stratigraphic and geochronologic contexts of mammoth (Mammuthus) and other Pleistocene fauna, Upper Missouri Basin (northern Great Plains and Rocky Mountains), U.S.A." Quaternary International. Third International Mammoth Conference, Dawson, Yukon. 142–143: 87–106. Bibcode:2006QuInt.142...87H. doi:10.1016/j.quaint.2005.03.007. ISSN 1040-6182.
  150. ^ Cassiliano, Michael L. (1999). "Biostratigraphy of Blancan and Irvingtonian Mammals in the Fish Creek-Vallecito Creek Section, Southern California, and a Review of the Blancan-Irvingtonian Boundary". Journal of Vertebrate Paleontology. 19 (1): 169–186. doi:10.1080/02724634.1999.10011131. ISSN 0272-4634. JSTOR 4523978.
  151. ^ Murray, Lyndon Keith (December 2008). "Effects of taxonomic and locality inaccuracies on biostratigraphy and biochronology of the Hueso and Tapiado formations in the Vallecito Creek-Fish Creek section, Anza-Borrego Desert, California". University of Texas at Austin. hdl:2152/15340.
  152. ^ Grayson, Donald K. (2006-11-01). "The Late Quaternary biogeographic histories of some Great Basin mammals (western USA)". Quaternary Science Reviews. 25 (21): 2964–2991. Bibcode:2006QSRv...25.2964G. doi:10.1016/j.quascirev.2006.03.004. ISSN 0277-3791.
  153. ^ "U-Bar Cave". www.utep.edu. Retrieved 2022-07-24.
  154. ^ Schultz, C. Bertrand; Howard, Edgar B.; Schultz, C. Bernard (1935). "The Fauna of Burnet Cave, Guadalupe Mountains, New Mexico". Proceedings of the Academy of Natural Sciences of Philadelphia. 87: 273–298. ISSN 0097-3157. JSTOR 4064215.
  155. ^ Harris, Arthur H. (1993). "Quaternary Vertebrates of New Mexico" (PDF). Vertebrate Paleontology in New Mexico, New Mexico Museum of Natural History and Science. Bulletin 2: 179–197.
  156. ^ Harris, A. H.; Findley, J. S. (1964-01-01). "Pleistocene-Recent fauna of the Isleta caves, Bernalillo County, New Mexico". American Journal of Science. 262 (1): 114–120. Bibcode:1964AmJS..262..114H. doi:10.2475/ajs.262.1.114. ISSN 0002-9599.
  157. ^ Morgan, Gary S.; Lucas, Spencer G.; Love, David (2009). "Cenozoic vertebrates from Socorro County, central New Mexico" (PDF). In Virgil Lueth; Spencer G. Lucas; Richard M. Chamberlin (eds.). New Mexico Geological Society Fall Field Conference Guidebook: 60 Geology of the Chupadera Mesa. pp. 321–336.
  158. ^ Morgan, Gary S.; Lucs, Spencer G. (2005-01-01). "Pleistocene vertebrates from southeastern New Mexico". KIP Articles.
  159. ^ Jefferson, George T. (2003), "Stratigraphy and paleontology of the middle to late Pleistocene Manix Formation, and paleoenvironments of the central Mojave River, Southern California", Paleoenvironments and paleohydrology of the Mojave and southern Great Basin deserts, Geological Society of America, doi:10.1130/0-8137-2368-x.43, ISBN 978-0-8137-2368-6, retrieved 2024-07-18
  160. ^ "Catalogue of Late Quaternary Vertebrates from California" (PDF). City of Santee. 26 March 2011.
  161. ^ Emslie, Steven D.; Mead, Jim I. (August 2020). "The Age and Vertebrate Paleontology of Labor-of-Love Cave, White Pine County, Nevada". Western North American Naturalist. 80 (3): 277–291. doi:10.3398/064.080.0301. ISSN 1527-0904. S2CID 225958789.
  162. ^ "LATE PLEISTOCENE AIRPORT LANE FOSSIL SITE, LA GRANDE ..." yumpu.com. Retrieved 2022-07-17.
  163. ^ Van Tassell, Jay; Rinehart, John; Mahrt, Laura (June 2014). "Late Pleistocene Airport Lane fossil site, La Grande, northeast Oregon" (PDF). Oregon Geology. 70 (1): 3–13 – via Oregon Department of Geology and Mineral Studies.
  164. ^ "The Spokesman-Review - Google News Archive Search". news.google.com. Retrieved 2022-07-20.
  165. ^ Harris, Arthur (2014-08-30). Pleistocene Vertebrates of Southwestern USA and Northwestern Mexico.
  166. ^ Harris, Arthur H. "Reconstruction of Mid Wisconsin Environments in Southern New Mexico" (PDF). National Geographic Research.
  167. ^ a b Eng-Ponce, Joaquin (August 2021). "Reconstruccion paeloambiental del yacimiento La Cinta-Portalitos, Michoacan-Guanajuato, Mexico (thesis)" (PDF). Faculty of Biology, Universidad Michoacana de San Nicolás de Hidalgo.
  168. ^ Lucas, Spencer G. (January 2008). "Late Pleistocene Vertebrate Fossil Assemblages From Jalisco, Mexico". Neogene Mammals. New Mexico Museum of Natural History and Science. Bulletin 44: 51–64 – via ResearchGate.
  169. ^ Hibbard, Claude W. (18 February 1955). "Pleistocene Vertebrates from the Upper Becerra (Becerra Superior) Formation, Valley of Tequixquiac, Mexico, with Notes on Other Pleistocene Forms". Contributions from the Museum of Paleontology. XII (5): 47–96. hdl:2027.42/48290.
  170. ^ Carranza-Castañeda, Oscar; Miller, Wade E. (16 September 1987). "Rediscovered type specimens and other important published Pleistocene mammalian fossils from Central Mexico". Journal of Vertebrate Paleontology. 7 (3): 335–341. Bibcode:1987JVPal...7..335C. doi:10.1080/02724634.1987.10011664.
  171. ^ Gobetz, Katrina E.; Martin, Larry D. (2001). "An Exceptionally Large Short-faced Bear (Arctodus simus) from the Late Pleistocene(?) /Early Holocene of Kansas" (PDF). Current Research in the Pleistocene. 18: 97–99. ISSN 8755-898X.
  172. ^ "Abstract: PLEISTOCENE VERTEBRATES FROM THE DOEDEN LOCAL FAUNA (ILLINOIAN/SANGAMONIAN?), YELLOWSTONE RIVER VALLEY, EASTERN MONTANA (Rocky Mountain - 55th Annual Meeting (May 7-9, 2003))". gsa.confex.com. Retrieved 2022-07-20.
  173. ^ McDonald, Andrew T.; Atwater, Amy L.; Dooley Jr, Alton C.; Hohman, Charlotte J.H. (2020-11-16). "The easternmost occurrence of Mammut pacificus (Proboscidea: Mammutidae), based on a partial skull from eastern Montana, USA". PeerJ. 8: e10030. doi:10.7717/peerj.10030. ISSN 2167-8359. PMC 7676352. PMID 33240588.
  174. ^ Hill, Christopher L; Wilson, Michael C (2002). "Fossil Arctodus from the Doeden Local Fauna (Illinoian/Sangamonian?), Eastern Montana". Unknown – via ResearchGate.
  175. ^ Froese, Duane; Stiller, Mathias; Heintzman, Peter D.; Reyes, Alberto V.; Zazula, Grant D.; Soares, André E. R.; Meyer, Matthias; Hall, Elizabeth; Jensen, Britta J. L.; Arnold, Lee J.; MacPhee, Ross D. E. (2017-03-28). "Fossil and genomic evidence constrains the timing of bison arrival in North America". Proceedings of the National Academy of Sciences. 114 (13): 3457–3462. Bibcode:2017PNAS..114.3457F. doi:10.1073/pnas.1620754114. ISSN 0027-8424. PMC 5380047. PMID 28289222.
  176. ^ a b Louguet-Lefebvre, Sophie (2013-12-15). "The Columbian mammoths from the Upper Pleistocene of Hot Springs (South Dakota, United States)". PALEO. Revue d'archéologie préhistorique (24): 149–171. doi:10.4000/paleo.2861. ISSN 1145-3370.
  177. ^ Johnson, Eileen (1986). "Late Pleistocene and Early Holocene Vertebrates and Paleoenvironments on the Southern High Plains, U.S.A." (PDF). Géographie physique et Quaternaire. 40 (3): 249–261. doi:10.7202/032647ar.
  178. ^ Smith, Felisa A.; Tomé, Catalina P.; Elliott Smith, Emma A.; Lyons, S. Kathleen; Newsome, Seth D.; Stafford, Thomas W. (February 2016). "Unraveling the consequences of the terminal Pleistocene megafauna extinction on mammal community assembly". Ecography. 39 (2): 223–239. Bibcode:2016Ecogr..39..223S. doi:10.1111/ecog.01779. ISSN 0906-7590. S2CID 4823663.
  179. ^ "Giant Short-Faced Bear | University of Iowa Museum of Natural History - The University of Iowa". mnh.uiowa.edu. Retrieved 2022-07-18.
  180. ^ Taylor, D. W. (1960). "Late Cenozoic molluscan faunas from the High Plains". USGS Report: 4. Bibcode:1960usgs.rept....4T. doi:10.3133/pp337. ISSN 2330-7102.
  181. ^ Harington, C. R. (1973). "A Short-Faced Bear From Ice Age Deposits at Lebret, Saskatchewan". Blue Jay. 31 (1). doi:10.29173/bluejay4039. ISSN 2562-5667. S2CID 222373512.
  182. ^ Harington, C. (1990). "Vertebrates of the Last Interglaciation in Canada: A Review, with New Data". Géographie physique et Quaternaire. 44 (3): 375–387. doi:10.7202/032837ar. ISSN 0705-7199.
  183. ^ Burns, James A.; Young, Robert R. (1994-02-01). "Pleistocene mammals of the Edmonton area, Alberta. Part I. The carnivores". Canadian Journal of Earth Sciences. 31 (2): 393–400. Bibcode:1994CaJES..31..393B. doi:10.1139/e94-036. ISSN 0008-4077.
  184. ^ Young, Robert R.; Burns, James A.; Smith, Derald G.; Arnold, L. David; Rains, R. Bruce (1994-08-01). "A single, late Wisconsin, Laurentide glaciation, Edmonton area and southwestern Alberta 2.3.CO;2". Geology. 22 (8): 683–686. doi:10.1130/0091-7613(1994)022<0683:ASLWLG>2.3.CO;2. ISSN 0091-7613.
  185. ^ a b Tankersley, Kenneth B. (26 May 1997). "Sheriden: A Clovis cave site in eastern North America". Geoarchaeology. 12 (6): 713–724. Bibcode:1997Gearc..12..713T. doi:10.1002/(SICI)1520-6548(199709)12:6<713::AID-GEA9>3.0.CO;2-1.
  186. ^ Wilson, Ronald C. (1985). "Vertebrate Remains in Kentucky Caves". In Percy H. Dougherty (ed.). Caves and Karst of Kentucky (PDF). Series XI. Vol. 12. Kentucky Geological Survey, University of Kentucky Lexington. p. 171. ISSN 0075-5613.
  187. ^ Colburn, Mona L. (July 2005). "Paleontological Inventory Project: Vertebrate Remains Found in Select Passages and Caves at Mammoth Cave National Park, Kentucky" (PDF). Illinois State Museum: 271, 281, 292.
  188. ^ Hawksley, Oscar (July 1965). "Short-Faced Bear (Arctodus) Fossils from Ozark Caves" (PDF). Bulletin of the National Speleological Society. 27 (3): 77–92.
  189. ^ Woodruff, Aaron L. (2016). "Description, Taphonomy, and Paleoecology of the Late Pleistocene Peccaries (Artiodactyla: Tayassuidae) from Bat Cave, Pulaski County, Missouri". Department of Geosciences, East Tennessee State University (Paper 3051) – via East Tennessee State University Digital Commons @ East Tennessee State University.
  190. ^ Woodruff, Aaron L.; Schubert, Blaine W. (2019-07-04). "Seasonal denning behavior and population dynamics of the late Pleistocene peccary Platygonus compressus (Artiodactyla: Tayassuidae) from Bat Cave, Missouri". PeerJ. 7: e7161. doi:10.7717/peerj.7161. ISSN 2167-8359. PMC 6612422. PMID 31308997.
  191. ^ Hawksley, Oscar; Reynolds, Jack F.; Foley, Robert F. (July 1973). "Pleistocene Vertebrate Fauna of Bat Cave, Pulaski County, Missouri" (PDF). Bulletin of the National Speleological Society. 35 (3): 61–87.
  192. ^ Santucci, Vincent L.; Kenworthy, Jason; Kerbo, Ron (2022-01-18). "An inventory of paleontological resources associated with national park service caves". KIP Articles.
  193. ^ Smith, Matthew D; Dorale, Jeffrey A; Johnson, Aaron W; Forir, Matthew D (2013). "A speleothem record of paleoenvironmental change from Riverbluff Cave, Missouri, U.S.A". iro.uiowa.edu. Retrieved 2022-07-26.
  194. ^ Simpson, Emily (2019-05-01). Paleoecology and Land-Use of Quaternary Megafauna from Saltville, Virginia (Master thesis). East Tennessee State University.
  195. ^ Ebersole, Jun A.; Ebersole, Sandy M. (December 2011). "Late Pleistocene Mammals of Alabama: A Comprehensive Faunal Review with 21 Previously Unreported Taxa" (PDF). Alabama Museum of Natural History Bulletin. 28: 24–25 – via University of Alabama.
  196. ^ Baghai-Riding, Nina L.; Husley, Danielle B.; Beck, Christine; Blackwell, Eric (December 2017). "Late Pleistocene Megafauna from Mississippi Alluvium Plain Gravel Bars" (PDF). Paludicola. 11 (3): 124–147 – via Rochester Institute of Vertebrate Paleontology.
  197. ^ Ruddell, Michael W. (December 1999). "Quaternary Vertebrate Paleoecology of the Central Mississippi Alluvial Valley; Implications for the Initial Human Occupation". Tennessee Research and Creative Exchange – via University of Tennessee, Knoxville.
  198. ^ Kurtén, Björn; Kaye, John M. (March 1982). "Late Quaternary Carnivora from the Black Belt, Mississippi". Boreas. 11 (1): 47–52. Bibcode:1982Borea..11...47K. doi:10.1111/j.1502-3885.1982.tb00519.x.
  199. ^ Kaye, John Morgan (1974). "Pleistocene Sediment and V ocene Sediment and Vertebrate Fossil Associations in the ossil Associations in the Mississippi Black Belt: a Genetic Approach". LSU Historical Dissertations and Theses. 2612 – via Louisiana State University.
  200. ^ Miller, Andrew (26 March 2021). "SC diver finds rare prehistoric bear tooth fossil in Cooper River". Post and Courier. Retrieved 2022-07-09.
  201. ^ Slaughter, Bob H. (1966). "The Moore Pit Local Fauna; Pleistocene of Texas". Journal of Paleontology. 40 (1): 78–91. ISSN 0022-3360. JSTOR 1301775.
  202. ^ David Webb, S.; Graham, Russell W.; Barnosky, Anthony D.; Bell, Christopher J.; Franz, Richard; Hadly, Elizabeth A.; Lundelius, Ernest L.; Gregory McDonald, H.; Martin, Robert A. (2003), Vertebrate paleontology, Developments in Quaternary Sciences, vol. 1, Elsevier, pp. 519–538, doi:10.1016/s1571-0866(03)01025-x, ISBN 978-0-444-51470-7, retrieved 2022-06-28
  203. ^ Harington, C. R. (1980). "Radiocarbon Dates on Some Quaternary Mammals and Artifacts from Northern North America". Arctic. 33 (4): 815–832. doi:10.14430/arctic2598. ISSN 0004-0843. JSTOR 40509084.
  204. ^ "The Ottawa naturalist: Vol. 25, no. 2 (May 1911) - Canadiana". www.canadiana.ca. Retrieved 2023-01-10.
  205. ^ a b Mann, Daniel H.; Groves, Pamela; Kunz, Michael L.; Reanier, Richard E.; Gaglioti, Benjamin V. (2013-06-15). "Ice-age megafauna in Arctic Alaska: extinction, invasion, survival". Quaternary Science Reviews. 70: 91–108. Bibcode:2013QSRv...70...91M. doi:10.1016/j.quascirev.2013.03.015. ISSN 0277-3791.
  206. ^ Monteath, Alistair J.; Gaglioti, Benjamin V.; Edwards, Mary E.; Froese, Duane (2021-12-28). "Late Pleistocene shrub expansion preceded megafauna turnover and extinctions in eastern Beringia". Proceedings of the National Academy of Sciences. 118 (52): e2107977118. Bibcode:2021PNAS..11807977M. doi:10.1073/pnas.2107977118. ISSN 0027-8424. PMC 8719869. PMID 34930836.
  207. ^ a b Murchie, Tyler J.; Monteath, Alistair J.; Mahony, Matthew E.; Long, George S.; Cocker, Scott; Sadoway, Tara; Karpinski, Emil; Zazula, Grant; MacPhee, Ross D. E.; Froese, Duane; Poinar, Hendrik N. (2021-12-08). "Collapse of the mammoth-steppe in central Yukon as revealed by ancient environmental DNA". Nature Communications. 12 (1): 7120. Bibcode:2021NatCo..12.7120M. doi:10.1038/s41467-021-27439-6. ISSN 2041-1723. PMC 8654998. PMID 34880234.
  208. ^ a b Barnes, I.; Matheus, P.; Shapiro, B.; Jensen, D.; Cooper, A. (2002-03-22). "Dynamics of Pleistocene Population Extinctions in Beringian Brown Bears". Science. 295 (5563): 2267–2270. Bibcode:2002Sci...295.2267B. doi:10.1126/science.1067814. ISSN 0036-8075. PMID 11910112. S2CID 5883943.
  209. ^ Leonard, Jennifer A.; Vilà, Carles; Fox-Dobbs, Kena; Koch, Paul L.; Wayne, Robert K.; Van Valkenburgh, Blaire (July 2007). "Megafaunal Extinctions and the Disappearance of a Specialized Wolf Ecomorph". Current Biology. 17 (13): 1146–1150. Bibcode:2007CBio...17.1146L. doi:10.1016/j.cub.2007.05.072. hdl:10261/61282. ISSN 0960-9822. PMID 17583509.
  210. ^ Pedersen, Mikkel W.; Ruter, Anthony; Schweger, Charles; Friebe, Harvey; Staff, Richard A.; Kjeldsen, Kristian K.; Mendoza, Marie L. Z.; Beaudoin, Alwynne B.; Zutter, Cynthia; Larsen, Nicolaj K.; Potter, Ben A. (2016). "Postglacial viability and colonization in North America's ice-free corridor" (PDF). Nature. 537 (7618): 45–49. Bibcode:2016Natur.537...45P. doi:10.1038/nature19085. PMID 27509852. S2CID 4450936.
  211. ^ Lucas, Spencer G.; Sullivan, Robert M. Fossil Record 6 Volume 2. New Mexico Museum of Natural History and Science.
  212. ^ a b Soibelzon, Leopoldo; Tarantini, Viviana Beatriz (January 2009). "Body mass estimation of extinct and extant South American bears (Ursidae, Tremarctinae)". Revista del Museo Argentino de Ciencias Naturales. 11 (2): 243–254. doi:10.22179/REVMACN.11.263 – via ResearchGate.
  213. ^ a b Arroyo-Cabrales, Joaquin; Johnson, Eileen; Graham, Russell W.; Pérez-Crespo, Victor (2016-07-24). North American ursid (mammalia: ursidae) defaunation from Pleistocene to recent. Vol. 33. ICBS Proceedings (Cranium). pp. 51–56. OCLC 1227719621.
  214. ^ Holliday, Vance T.; Johnson, Eileen; Haas, Herbert; Stuckenrath, Robert (1983). "Radiocarbon Ages from the Lubbock Lake Site, 1950-1980: Framework for Cultural and Ecological Change on the Southern High Plains". Plains Anthropologist. 28 (101): 165–182. doi:10.1080/2052546.1983.11909122. ISSN 0032-0447. JSTOR 25668371.
  215. ^ Brian G. Redmond (March 2006). "Before the Western Reserve: An Archaeological History of Northeast Ohio" (PDF). The Cleveland Museum of Natural History. p. 2. Retrieved January 28, 2020.
  216. ^ Kenworthy, Jason P.; Santucci, Vincent L.; McNerney, Michaleen; Snell, Kathryn (August 2005). "Paleontological Resource Inventory and Monitoring: Upper Columbian Basin Network" (PDF). National Park Service (U.S. Department of the Interior). TIC# D-259: 51.
  217. ^ Chadez, Jenifer; Sappington, Robert Lee (2017-12-01). "The Holocene exploitation of mammals in the Clearwater and lower Snake River regions of north-central Idaho". Journal of Archaeological Science: Reports. 16: 258–265. Bibcode:2017JArSR..16..258C. doi:10.1016/j.jasrep.2017.09.030. ISSN 2352-409X.
  218. ^ Grayson, Donald K.; Meltzer, David J. (2002). "Clovis Hunting and Large Mammal Extinction: A Critical Review of the Evidence". Journal of World Prehistory. 16 (4): 313–359. doi:10.1023/A:1022912030020. S2CID 162794300.
  219. ^ Cannon, Michael D.; Meltzer, David J. (2004-10-01). "Early Paleoindian foraging: examining the faunal evidence for large mammal specialization and regional variability in prey choice". Quaternary Science Reviews. 23 (18): 1955–1987. Bibcode:2004QSRv...23.1955C. doi:10.1016/j.quascirev.2004.03.011. ISSN 0277-3791.
  220. ^ Reid, Kenneth C. (2017-07-20). "Idaho beginnings: A review of the evidence". Quaternary International. After Anzick: Reconciling New Genomic Data and Models with the Archaeological Evidence for Peopling of the Americas. 444: 72–82. Bibcode:2017QuInt.444...72R. doi:10.1016/j.quaint.2017.03.040. ISSN 1040-6182.
  221. ^ Kenady, Stephen M.; Wilson, Michael C.; Schalk, Randall F.; Mierendorf, Robert R. (March 2011). "Late Pleistocene butchered Bison antiquus from Ayer Pond, Orcas Island, Pacific Northwest: Age confirmation and taphonomy". Quaternary International. 233 (2): 130–141. Bibcode:2011QuInt.233..130K. doi:10.1016/j.quaint.2010.04.013.
  222. ^ Geist, Valerius (1989), "Did Large Predators keep Humans out of North America?" (PDF), in Clutton-Brock, Juliet (ed.), The Walking larder: patterns of domestication, pastoralism, and predation, Unwin Hyman, pp. 282–294, ISBN 0-0444-5013-3, archived from the original (PDF) on 16 December 2008
  223. ^ a b Pigati, Jeffrey S.; Springer, Kathleen B.; Honke, Jeffrey S.; Wahl, David; Champagne, Marie R.; Zimmerman, Susan R. H.; Gray, Harrison J.; Santucci, Vincent L.; Odess, Daniel; Bustos, David; Bennett, Matthew R. (2023-10-06). "Independent age estimates resolve the controversy of ancient human footprints at White Sands". Science. 382 (6666): 73–75. Bibcode:2023Sci...382...73P. doi:10.1126/science.adh5007. ISSN 0036-8075. PMID 37797035. S2CID 263672291.
  224. ^ a b c Boëda, Eric; Gruhn, Ruth; Vialou, Agueda Vilhena; Aschero, Carlos; Vialou, Denis; Pino, Mario; Gluchy, Maria; Pérez, Antonio; Ramos, Marcos Paulo (2021-01-02). "The Chiquihuite Cave, a Real Novelty? Observations about the Still-ignored South American Prehistory". PaleoAmerica. 7 (1): 1–7. doi:10.1080/20555563.2020.1851500. ISSN 2055-5563. S2CID 230533453.
  225. ^ a b Pansani, Thais R.; Pobiner, Briana; Gueriau, Pierre; Thoury, Mathieu; Tafforeau, Paul; Baranger, Emmanuel; Vialou, Águeda V.; Vialou, Denis; McSparron, Cormac; de Castro, Mariela C.; Dantas, Mário A. T.; Bertrand, Loïc; Pacheco, Mírian L. A. F. (2023-07-12). "Evidence of artefacts made of giant sloth bones in central Brazil around the last glacial maximum". Proceedings of the Royal Society B: Biological Sciences. 290 (2002). doi:10.1098/rspb.2023.0316. ISSN 0962-8452. PMC 10336383. PMID 37434527.
  226. ^ a b c Gruhn, Ruth (2023-07-03). "An Anthropological Conception of the Initial Peopling of the Americas". PaleoAmerica. 9 (3): 167–173. doi:10.1080/20555563.2023.2278948. ISSN 2055-5563. S2CID 265285459.
  227. ^ Graf, Kelly E.; Buvit, Ian (2017-12-01). "Human Dispersal from Siberia to Beringia: Assessing a Beringian Standstill in Light of the Archaeological Evidence". Current Anthropology. 58 (S17): S583–S603. doi:10.1086/693388. ISSN 0011-3204. S2CID 149080106.
  228. ^ Harington, C. R.; Morlan, Richard E. (2002). "Evidence for Human Modification of a Late Pleistocene Bison (Bison sp.) Bone from the Klondike District, Yukon Territory, Canada". Arctic. 55 (2): 143–147. doi:10.14430/arctic698. ISSN 0004-0843. JSTOR 40512447.
  229. ^ Holen, Steven R.; Harington, C. Richard; Holen, Kathleen A. (2017). "New Radiocarbon Ages on Percussion-Fractured and Flaked Proboscidean Limb Bones from Yukon, Canada". Arctic. 70 (2): 141–150. doi:10.14430/arctic4645. ISSN 0004-0843. JSTOR 26379757.
  230. ^ Goebel, Ted; Hoffecker, John F.; Graf, Kelly E.; Vachula, Richard S. (June 2022). "Archaeological reconnaissance at Lake E5 in the Brooks Range, Alaska and implications for the early human biomarker record of Beringia". Quaternary Science Reviews. 286: 107553. Bibcode:2022QSRv..28607553G. doi:10.1016/j.quascirev.2022.107553. S2CID 248736952.
  231. ^ Bourgeon, Lauriane; Burke, Ariane; Higham, Thomas (2017-01-06). "Earliest Human Presence in North America Dated to the Last Glacial Maximum: New Radiocarbon Dates from Bluefish Caves, Canada". PLOS ONE. 12 (1): e0169486. Bibcode:2017PLoSO..1269486B. doi:10.1371/journal.pone.0169486. ISSN 1932-6203. PMC 5218561. PMID 28060931.
  232. ^ Bourgeon, Lauriane (2021-06-01). "Revisiting the mammoth bone modifications from Bluefish Caves (YT, Canada)". Journal of Archaeological Science: Reports. 37: 102969. Bibcode:2021JArSR..37j2969B. doi:10.1016/j.jasrep.2021.102969. ISSN 2352-409X. S2CID 234816694.
  233. ^ Ardelean, Ciprian F.; Becerra-Valdivia, Lorena; Pedersen, Mikkel Winther; Schwenninger, Jean-Luc; Oviatt, Charles G.; Macías-Quintero, Juan I.; Arroyo-Cabrales, Joaquin; Sikora, Martin; Ocampo-Díaz, Yam Zul E.; Rubio-Cisneros, Igor I.; Watling, Jennifer G.; de Medeiros, Vanda B.; De Oliveira, Paulo E.; Barba-Pingarón, Luis; Ortiz-Butrón, Agustín (2020-08-06). "Evidence of human occupation in Mexico around the Last Glacial Maximum". Nature. 584 (7819): 87–92. Bibcode:2020Natur.584...87A. doi:10.1038/s41586-020-2509-0. ISSN 0028-0836. PMID 32699412. S2CID 256819465.
  234. ^ Pichardo, M. (1997). "Valsequillo biostratigraphy: New evidence for Pre-Clovis date". Anthropologischer Anzeiger. 55 (3/4): 233–246. doi:10.1127/anthranz/55/1997/233. ISSN 0003-5548. JSTOR 29540729.
  235. ^ Gonzalez, Sofia; Huddart, David (2008). "The Late Pleistocene Human Occupation of Mexico". FUMDHAMentos VII – via ResearchGate.
  236. ^ a b Gruhn, Ruth (2020-08-06). "Evidence grows that peopling of the Americas began more than 20,000 years ago". Nature. 584 (7819): 47–48. Bibcode:2020Natur.584...47G. doi:10.1038/d41586-020-02137-3. ISSN 0028-0836. PMID 32699366. S2CID 220717778.
  237. ^ a b Rowe, Timothy B.; Stafford, Thomas W.; Fisher, Daniel C.; Enghild, Jan J.; Quigg, J. Michael; Ketcham, Richard A.; Sagebiel, J. Chris; Hanna, Romy; Colbert, Matthew W. (2022). "Human Occupation of the North American Colorado Plateau ∼37,000 Years Ago". Frontiers in Ecology and Evolution. 10. doi:10.3389/fevo.2022.903795. ISSN 2296-701X.
  238. ^ Gruhn, Ruth (2022), Miotti, Laura; Salemme, Monica; Hermo, Darío (eds.), "To the End of the World: Southern Patagonia in Models of the Initial Peopling of the Western Hemisphere", Archaeology of Piedra Museo Locality, The Latin American Studies Book Series, Cham: Springer International Publishing, pp. 449–456, doi:10.1007/978-3-030-92503-1_16, ISBN 978-3-030-92502-4, S2CID 246571694, retrieved 2023-12-11
  239. ^ Karrow, P.F.; Morgan, G.S.; Portell, R. W.; Simons, E.; Auffenberg, K. (1996-12-31), "Middle Pleistocene (early Rancholabrean) vertebrates and associated marine and non-marine invertebrates from Oldsmar, Pinellas County, Florida", Palaeoecology and Palaeoenvironments of Late Cenozoic Mammals, University of Toronto Press, pp. 97–133, doi:10.3138/9781487574154-009, ISBN 978-1-4875-7415-4, retrieved 2024-01-23
  240. ^ Feranec, Robert S.; Hadly, Elizabeth A.; Blois, Jessica L.; Barnosky, Anthony D.; Paytan, Adina (2007). "Radiocarbon Dates from the Pleistocene Fossil Deposits of Samwel Cave, Shasta County, California, USA". Radiocarbon. 49 (1): 117–121. Bibcode:2007Radcb..49..117F. doi:10.1017/S0033822200041941. S2CID 130708736.
  241. ^ a b Stuart, Anthony John (May 2015). "Late Quaternary megafaunal extinctions on the continents: a short review: LATE QUATERNARY MEGAFAUNAL EXTINCTIONS". Geological Journal. 50 (3): 338–363. doi:10.1002/gj.2633. S2CID 128868400.
  242. ^ Haynes, Gary (2013-02-08). "Extinctions in North America's Late Glacial landscapes". Quaternary International. Peopling the last new worlds: the first colonisation of Sahul and the Americas. 285: 89–98. Bibcode:2013QuInt.285...89H. doi:10.1016/j.quaint.2010.07.026. ISSN 1040-6182.
  243. ^ Mitchell, Kieren J.; Bover, Pere; Salis, Alexander T.; Mudge, Caitlin; Heiniger, Holly; Thompson, Mary; Hockett, Bryan; Weyrich, Laura S.; Cooper, Alan; Meachen, Julie A. (November 2021). "Evidence for Pleistocene gene flow through the ice-free corridor from extinct horses and camels from Natural Trap Cave, Wyoming". Quaternary International. 647–648: 71–80. doi:10.1016/j.quaint.2021.11.017. S2CID 244706923.
  244. ^ Stynder, Deano D.; Kupczik, Kornelius (September 2012). "Tooth Root Morphology in the Early Pliocene African Bear Agriotherium africanum (Mammalia, Carnivora, Ursidae) and its Implications for Feeding Ecology". Journal of Mammalian Evolution. 20 (3): 227–237. doi:10.1007/s10914-012-9218-x. ISSN 1064-7554. S2CID 254692536.
  245. ^ Bocherens, H.; Emslie, S. D.; Billiou, D.; Mariotti A. (1995). "Stable isotopes (13C, 15N) and paleodiet of the giant short-faced bear (Arctodus simus)". C R Acad Sci. 320: 779–784.
  246. ^ Stuart, Anthony J.; Lister, Adrian M. (2012-09-19). "Extinction chronology of the woolly rhinoceros Coelodonta antiquitatis in the context of late Quaternary megafaunal extinctions in northern Eurasia". Quaternary Science Reviews. 51: 1–17. Bibcode:2012QSRv...51....1S. doi:10.1016/j.quascirev.2012.06.007. ISSN 0277-3791.
  247. ^ "Beringia: Lost World of the Ice Age (U.S. National Park Service)". www.nps.gov. Retrieved 2022-06-09.
  248. ^ Blinnikov, Mikhail S.; Gaglioti, Benjamin V.; Walker, Donald A.; Wooller, Matthew J.; Zazula, Grant D. (2011-10-01). "Pleistocene graminoid-dominated ecosystems in the Arctic". Quaternary Science Reviews. 30 (21): 2906–2929. Bibcode:2011QSRv...30.2906B. doi:10.1016/j.quascirev.2011.07.002. ISSN 0277-3791.
  249. ^ McHorse, Brianna K.; Orcutt, John D.; Davis, Edward B. (2012-04-15). "The carnivoran fauna of Rancho La Brea: Average or aberrant?". Palaeogeography, Palaeoclimatology, Palaeoecology. 329–330: 118–123. Bibcode:2012PPP...329..118M. doi:10.1016/j.palaeo.2012.02.022. ISSN 0031-0182.
  250. ^ Wang, Xiaoming; Martin, Larry (1993-01-01). "Late Pleistocene, paleoecology and large mammal taphonomy, Natural Trap Cave, Wyoming". National Geographic Research & Exploration. 9: 422–435.
  251. ^ Veitschegger, Kristof (2017-06-05). "The effect of body size evolution and ecology on encephalization in cave bears and extant relatives". BMC Evolutionary Biology. 17 (1): 124. Bibcode:2017BMCEE..17..124V. doi:10.1186/s12862-017-0976-1. ISSN 1471-2148. PMC 5460516. PMID 28583080.