Panthera spelaea, commonly known as the cave lion (or less commonly as the steppe lion), is an extinct Panthera species that was native to Eurasia and northwest North America during the Pleistocene epoch. Genetic analysis of ancient DNA has revealed that while closely related, it was a distinct species genetically isolated from the modern lion ( Panthera leo), with the genetic divergence between the two species estimated at around 500,000 years ago.
The earliest fossils of the P. spelaea lineage (either regarded as the separate species Panthera fossilis or the subspecies P. spelaea fossilis) in Eurasia date to around 700,000 years ago (with possible late Early Pleistocene records). It is closely related and probably ancestral to the American lion ( Panthera atrox). The species ranged from Western Europe to eastern Beringia in North America, and was a prominent member of the mammoth steppe fauna, and an important apex predator across its range along with other large carnivores like Cave hyena, which cave lions came into conflict with.
It closely resembled living lions with a coat of yellowish-grey fur though unlike extant lions, males appear to have lacked manes. Whether or not cave lions lived in social groups like living lions is uncertain, but they are frequently suggested to have been largely solitary, similar to living Tiger.
Panthera spelaea interacted with both Neanderthals and modern humans, who used their pelts and in the case of the latter, depicted them in artistic works.
Cave lions became extinct about 13,000 years ago as part of the end-Pleistocene extinction event, the precise cause of which is unknown, though climatic change, changes in prey abundance, and competition with other carnivores and humans have been suggested as possible causal factors.
Several anatomical studies of remains of Panthera spelaea were conducted during the early-mid 19th century, who found the morphology of the species most similar to Lion, Tiger and Jaguar. A monograph by W. Dawkins and W. Sandford studying P. spelaea published in 1868 found that it had closest affinities with the modern lion. At the end of the 19th century, the earliest remains of P. spelaea from Siberia were reported by M. Tschersky, who mistook them for those of a tiger. During the 20th century and the first decade of the 21st century, Panthera spelaea was often regarded as a subspecies of the modern lion, and therefore as Panthera leo spelaea. However, other authors considered the cave lion to be more closely related to the tiger, based in part on a comparison of skull shapes, with some proposing that it should be considered a subspecies of the tiger as Panthera tigris spelaea. Analysis of cave lion mitochondrial genomes published in 2004 supported the modern lion as the closest relative of P. spelaea, with this result being later confirmed by analysis of the nuclear genome. Results from morphological studies showed that it is distinct in cranial and dental anatomy to justify the Species status of Panthera spelaea. Results of genetic studies also support this assessment.
In 2001, the subspecies Panthera spelaea vereshchagini was proposed for seven specimens found in Siberia and Yukon, which have smaller skulls and teeth than the average P. spelaea. Before 2020, genetic analysis using ancient DNA provided no evidence for their distinct subspecific status; DNA signatures from P. spelaea from Europe and Alaska were indistinguishable, suggesting one large panmictic population. However, analysis of mitochondrial genome sequences from 31 cave lions showed that they fall into two monophyletic . One lived across western Europe and the other was restricted to Beringia during the Pleistocene. For this reason, the Beringian population is considered a distinct subspecies, P. s. vereshchagini.
Cladogram after Tseng et al. (2014):
The arrival of Panthera (spelaea) fossilis in Europe was part of a faunal turnover event around the Early-Middle Pleistocene transition in which many of the species that characterised the preceding late Villafranchian became extinct. In the carnivore guild, this notably included the giant hyena Pachycrocuta and the sabertooth cat Megantereon. Following the arrival of Panthera (spelaea) fossilis the lion-sized sabertooth cat Homotherium and the "European jaguar" Panthera gombaszoegensis became much rarer, ultimately becoming extinct in Europe during the late Middle Pleistocene, with competition with lions suggested to be a likely important factor.
Specimens intermediate between P. fossilis and Late Pleistocene P. spelaea are referred to as the subspecies P. s. intermedia. The transition from P. fossilis to Late Pleistocene P. spelaea shows significant reduction in body size, as well as changes in skull and tooth morphology. Mitochondrial DNA sequence data from fossil lion remains show that the American lion represents a sister group of Late Pleistocene P. spelaea, and likely arose when an early P. spelaea population became isolated south of the Cordilleran Ice Sheet. Initially this was suggested to be around 340,000 years ago, but later studies suggested that the split between the two species was probably younger, around 165,000 years ago, consistent with the late first appearance of P. spelaea in Eastern Beringia (now Alaska and adjacent regions) during the Illinoian (around 190-130,000 years ago).
P. spelaea had a relatively longer and narrower muzzle compared to that of the extant lion, with the Zygomatic bone region being strongly arched, with the carnassial teeth having differences in cusp morphology (displaying preparastyles). Like modern lions, females were smaller than males. Compared to the earlier P. ( spelaea) fossilis, Late Pleistocene P. spelaea spelaea differs (in addition to previously mentioned size differences) in having larger incisor teeth, more narrow and flattened Canine tooth, as well narrower upper and lower third and fourth premolars, which display some differences in cusp morphology, with the lower first molar being narrower and more elongate. The orbits (eye sockets) of P. spelaea spelaea are also relatively larger and muzzle marginally narrower compared to P. ( spelaea) fossilis, with the nasal region also being proportionally narrower, while the postorbital and mastoid regions of the skull are wider, with the Tympanic bulla being more inflated.SABOL, Martin. Panthera fossilis (REICHENAU, 1906) (Felidae, Carnivora) from Za Hájovnou Cave (Moravia, the Czech Republic): a fossil record from 1987–2007. Fossil Imprint / Acta Musei Nationalis Pragae, Series B – Historia Naturalis Prague: National Museum, 2014, 70(1-2), 59-70. ISSN 2533-4050 (tisk), 2533-4069 (online).
In 2016, hair found near the Maly Anyuy River was identified as cave lion hair through DNA analysis. Comparison with hair of a modern lion revealed that cave lion hair was probably similar in colour as that of the modern lion, though slightly lighter. In addition, the cave lion is thought to have had a very thick and dense undercoat comprising closed and compressed yellowish-to-white wavy downy hair with a smaller mass of darker-coloured guard hairs, possibly an adaptation to the Ice age climate. While juveniles fur coat colour was yellowish, adult cave lions are suggested to have had grey fur.
The cave lion probably inhabited predominantly open habitats such as steppe and grasslands although it would have also occurred in open woodlands as well. While during the Last Glacial Period it was often associated with cold environments, the species also inhabited temperate environments, such as in Europe during the Last Interglacial/Eemian.
Isotopic analyses of bone collagen samples extracted from remains in Europe and East Beringia indicate that reindeer were particularly prominent in the diet of cave lions in these regions during the Last Glacial Period. Cave lions also seem to have opportunistically preyed on the cubs of Cave bear, with adult cave bears also likely being targeted at least on occasion. Isotopic analysis of other European specimens suggests a diet including wild horse, woolly mammoth and cave bears for these individuals. It may have sought out hibernating bears in montane caves as a food source during the winter. Bite marks found on the bones of straight-tusked elephants in Neumark Nord, Germany, dating to the Last Interglacial, have been suggested to be the result of scavenging by cave lions.
Other possible prey species were giant deer, red deer, muskox, aurochs, wisent, bison priscus, and young woolly rhinoceros. It likely competed for prey with the European leopards, cave hyenas, brown bears and grey wolves in Eurasia, along with Arctodus, the sabertooth cat Homotherium, and Beringian wolf in Beringia.
Isotopic analysis on cave lions by Hervé Bocherens and colleagues lead them to suggest that cave lions may have been solitary, due to cave lions shifting their diets after the disappearance of cave hyenas, carcasses being consumed the cave hyenas as well, suggests they were at a competitive disadvantage, and the scattering of isotopic data between individuals. Within mountain ranges and higher altitude environments, cave lions may have also been solitary or hunt in mating pairs, much like today’s lions. Lions tend to hunt in prides in altitudes below 1,500 meters, but within higher altitudes, they tend to be solitary or hunt in mating pairs. This proposed behavior for cave lions is further supported by the ratios of males and females from Moravian Karst being 1:1.
Cave lion cubs appear to have lived in dens during their earliest stages of life, like modern lion cubs and were likely solely raised by females, like living Panthera species.
Following the arrival of modern humans into Europe into the Upper Paleolithic, they drew cave paintings of cave lions, engraved their likeness on bones and created sculptures of them, including the famous anthropomorphic lion-man ( Löwenmensch) figure from Hohlenstein-Stadel cave in Germany dating to around 41-35,000 years ago with the body of a human and the head of a lion. Cave lion canines with perforated holes may have been worn as personal ornaments. Decorated stones with engravings representing cave lions have been found in southern Italy. Modern humans also like Neanderthals utilized their pelts, as evidenced by phalanges found at the La Garma site in Spain dating to the Magdalenian, around 16,800 years ago. Some bones of cave lions found in Upper Paleolithic layers (such as the Aurignacian and Gravettian) of the Swabian Jura of southern Germany display cut marks and modification into tools,Kitagawa, K., Krönneck, P., Conard, N. J. & Münzel, S. C. Exploring cave use and exploitation among cave bears, carnivores and hominins in the Swabian Jura. Germany. J. Taphon. 10, 439–461 (2012). which may represent evidence of hunting, though evidence of hunting cave lions by modern humans during the Upper Paleolithic is uncommon.
The extinction formed part of the broader end-Pleistocene extinction event, in which most large terrestrial mammals globally became extinct, including many large carnivores.
In 2017, another frozen specimen, thought to be a lion cub, was found in Yakutia on the banks of the Tirekhtyakh River (), a tributary of the Indigirka River. This male cub was thought to be slightly older than the 2015 cubs at the time of its death; it is estimated to have been around one and a half to two months. In 2018, another preserved carcass of a cub was found in a location away. It was considered to be around a month old when it died approximately 50,000 years ago, and presumed to be a sibling of the male cub. However, carbon date showed them to have lived about 15,000 years apart, with the female estimated to have lived 28,000 years ago, and the male 43,448 years ago. Both cubs were well preserved, albeit with a few damages, with the female possibly being the "best preserved" animal discovered from the Ice age.
Evolution
Description
Distribution and habitat
Paleobiology
Ecology
Social behavior
Relationship with humans
Extinction
Mummified specimens
Notes
See also
External links
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