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==Description==
==Description==
⚫
[[File:Wolf cranium labelled.jpg|thumb|300px|Diagram of a wolf skull with key features labelled]]


The short-legged ''C. l. spelaeus'' was a glacial [[mammoth steppe]]-adapted white wolf. It first appeared 320,000 years ago ([[Marine isotope stages|MIS 8]], [[Middle Pleistocene]]), and disappeared along with the mammoth steppe and cave bear fauna at the end of the Late Pleistocene, somewhere between 24,000-12,000 years ago (MIS 2). Compared with the modern day [[Arctic wolf]] ''C. l. arctos'' and the Siberian [[Tundra wolf]] ''C. l. albus'', its legs are shorter than the Tundra wolf but similar to the Arctic wolf and may be its ancestor.<ref name=Diedrich2022/>
The short-legged ''C. l. spelaeus'' was a glacial [[mammoth steppe]]-adapted white wolf. It first appeared 320,000 years ago ([[Marine isotope stages|MIS 8]], [[Middle Pleistocene]]), and disappeared along with the mammoth steppe and cave bear fauna at the end of the Late Pleistocene, somewhere between 24,000-12,000 years ago (MIS 2). Compared with the modern day [[Arctic wolf]] ''C. l. arctos'' and the Siberian [[Tundra wolf]] ''C. l. albus'', its legs are shorter than the Tundra wolf but similar to the Arctic wolf and may be its ancestor.<ref name=Diedrich2022/>
Line 48: Line 47:


Its bone proportions are close to those of the [[Northwestern wolf|Canadian Arctic-boreal mountain-adapted timber wolf]] and a little larger than those of the modern [[Eurasian wolf|European wolf]]. Some postcranial bones have similarly large proportions to those from the Sophie's and Große Teufels Caves,<ref name=diedrichC5/> where the bone sizes are closer to those of Scandinavian Arctic and Canadian Columbian wolf subspecies than to those of the smaller European wolves. Bone sizes are one-eighth larger than European wolves, and this wolf was a specialized Late Pleistocene wolf [[ecomorph]].<ref name=diedrichC6/>
Its bone proportions are close to those of the [[Northwestern wolf|Canadian Arctic-boreal mountain-adapted timber wolf]] and a little larger than those of the modern [[Eurasian wolf|European wolf]]. Some postcranial bones have similarly large proportions to those from the Sophie's and Große Teufels Caves,<ref name=diedrichC5/> where the bone sizes are closer to those of Scandinavian Arctic and Canadian Columbian wolf subspecies than to those of the smaller European wolves. Bone sizes are one-eighth larger than European wolves, and this wolf was a specialized Late Pleistocene wolf [[ecomorph]].<ref name=diedrichC6/>

⚫
[[File:Wolf cranium labelled.jpg|thumb|300px|Diagram of a wolf skull with key features labelled]]


During the Late Pleistocene, ''C. l. spelaeus'' exhibited a changed skeletal development due to the harsh climatic and environmental conditions, and a preference for taking larger prey. This resulted in a larger and more robust wolf with a shortened [[rostrum (anatomy)|rostrum]], a pronounced development of the [[temporalis]] muscles, and proportionally enlarged and wider [[premolars]] and [[carnassial]]s. These features were specialised adaptations for the processing of fast-freezing carcasses associated with the hunting and scavenging of larger prey. Some populations of ''C. l. spelaeus'' showed an increase in tooth breakage when compared with the extant ''C. lupus'' because they were habitual bone crackers. The large dimensions, robust build and cranio-dental adaptations formed at this time enabled these wolves to hunt larger prey, making the adult [[Steppe Bison]] ''Bison priscus'' a more attainable target than for their ''C. lupus'' relatives.<ref name=marciszak2023/>
During the Late Pleistocene, ''C. l. spelaeus'' exhibited a changed skeletal development due to the harsh climatic and environmental conditions, and a preference for taking larger prey. This resulted in a larger and more robust wolf with a shortened [[rostrum (anatomy)|rostrum]], a pronounced development of the [[temporalis]] muscles, and proportionally enlarged and wider [[premolars]] and [[carnassial]]s. These features were specialised adaptations for the processing of fast-freezing carcasses associated with the hunting and scavenging of larger prey. Some populations of ''C. l. spelaeus'' showed an increase in tooth breakage when compared with the extant ''C. lupus'' because they were habitual bone crackers. The large dimensions, robust build and cranio-dental adaptations formed at this time enabled these wolves to hunt larger prey, making the adult [[Steppe Bison]] ''Bison priscus'' a more attainable target than for their ''C. lupus'' relatives.<ref name=marciszak2023/>

Revision as of 04:55, 24 January 2024

Cave wolf
Temporal range: Middle Pleistocene - Late Pleistocene
320,000—12,000 years ago
The Goldfuss holotype,[1] Berlin's Natural History Museum
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Order: Carnivora
Family: Canidae
Genus: Canis
Species:
C. lupus
Subspecies:
†C. l. spelaeus
Trinomial name
†Canis lupus spelaeus
Goldfuss, 1823[2]
Synonyms[5]

C. l. brevis Kuzmina and Sablin, 1994[3]
C. l. maximus Boudadi-Maligne, 2012[4]

The cave wolf (Canis lupus spelaeus) is an extinct glacial mammoth steppe-adapted white wolf that lived during the Middle Pleistocene to the Late Pleistocene. It inhabited Europe, where its remains have been found in many caves. Its habitat included the mammoth steppe grasslands and boreal needle forests.[6]

Taxonomy

The large wolf C. l. spelaeus Georg August Goldfuss, 1823 was first described based on a wolf pup skull found in the Zoolithen Cave located at Gailenreuth, Bavaria, Germany.[2] In Germany, cave wolf populations are known from three caves separated by a few kilometers from each other that are located on the Franconia Karst along the Wiesent and Ahorn River vallies in the Upper Franconia region of the state of Bavaria, Germany. Sophie's Cave sits on the northwest slope of the Ailsbach Valley near Rabenstein Castle in the Ahorntal municipality. Große Teufels Cave (Big Devil's Cave) and the Zoolithen Cave are located nearby.[7] They are also known from Hermann's Cave in the village of Rübeland near the town of Wernigerode, in the district of Harz, Saxony-Anhalt, Germany.[8]

These large wolves have not been studied in any degree of depth,[9] and their relationship to modern wolves has not been clarified using DNA. All of the top predators in Europe commenced going extinct with the loss of the pleistocene megafauna when conditions became colder during the peak of the Last Glacial Maximum around 23,000 years ago. The last cave wolves used the side branches of the main caves to protect their pups from the cold climate.[10] During this time the cave wolf was replaced by a smaller wolf-type, which then disappeared along with the reindeer, to finally be replaced by the Holocene warm-period European wolf Canis lupus lupus.[9]

Canis lupus bohemica

In 2022, a new species Canis lupus bohemica was taxonomically described after having been discovered in the Bat Cave system located near Srbsko, Central Bohemia, Czech Republic. The Bohemian wolf is an extinct short-legged wolf that first appeared 800,000 years ago (MIS 20, the Rhumian Interglacial of the early Cromerian stage, Middle Pleistocene) and once inhabited what was part of the mammoth steppe. It is proposed as the ancestor of Canis lupus mosbachensis. In comparison, C. etruscus appears to be the ancestor of the Afro-Eurasian jackal.[6]

In Hungary in 1969, a tooth (the premolar of the Maxilla) was found which dated to the Middle Pleistocene, and was assessed as being midway between that of Canis mosbachensis and the cave wolf Canis lupus spelaeus, but leaning towards C.l. spelaeus.[11] During the late Middle Pleistocene around 600,000 years ago, the Bohemian wolf diversified into two wolf lineages that specialized for different environmental and climatic conditions. One was a southern interglacial (warm climate) grey wolf of Europe which was to become the Mosbach wolf, and the other a northern glacial white wolf of Eurasia which was to become C. l. spelaeus.[6]

Canis lupus brevis

The Don wolf Canis lupus brevis Kuzmina and Sablin, 1994 is an extinct wolf whose fossil remains were found at the Kostenki I Late Pleistocene site by the Don River at Kostyonki, Voronezh Oblast, Russia and reported in 1994. Based on the size of its dental rows, the Don wolf was bigger than modern wolves from the tundra or the Middle Russian taiga. The length of its P4 was longer than the row of its molars M1-M2, which is different to the Late Pleistocene wolves from the Caucasus or the Ural Mountains. Its main characteristic was its shorter legs, due to shorter humerus, radius, metacarpals, tibia, and metatarsals.[3] This warm climate grey wolf existed at the same time as C. l. spelaeus.[6] In 2009, a study compared the skull of one of these wolves to those found in Western Europe, and proposed that C. l. brevis of eastern Europe and C. l. spelaeus of western Europe are taxonomic synonyms for the same subspecies.[5][6] These were both comparable to the remains of a 16,000 YBP wolf skull found on the Taimyr peninsula in far northern Siberia.[5]

Canis lupus maximus

The large wolf Canis lupus maximus Boudadi-Maligne, 2012 was a subspecies larger than all other known fossil and extant wolves from Western Europe. The fossilized remains of this Late Pleistocene subspecies were found across a wide area of south-western France at: Jaurens cave, Nespouls, Corrèze dated 31,000 YBP; Maldidier cave, La Roque-Gageac, Dordogne dated 22,500 YBP; and Gral pit-fall, Sauliac-sur-Célé, Lot dated 16,000 YBP. The wolf's long bones are 10 percent longer than those of extant European wolves and 20 percent longer than its probable ancestor, C. l. lunellensis. The teeth are robust, the posterior denticules on the lower premolars p2, p3, p4 and upper P2 and P3 are highly developed, and the diameter of the lower carnassial (m1) were larger than any known European wolf.[4]

Wolf body size in Europe has followed a steady increase from their first appearance up to the peak of the Last Glacial Maximum. The size of these wolves are thought to be an adaptation to a cold environment (Bergmann's rule) and plentiful game as their remains have been found in association with reindeer fossils.[4]

In 2022, a paleontologist proposed that C. l. maximus was a taxonomic synonym for C. l. spelaeus.[6]

Italian wolves

A 2014 study found wolves in Late Pleistocene Italy were comparable in tooth morphology – and therefore in size – with C. l. maximus from France. These wolves were found near Avetrana, Taranto and near Buco del Frate, Brescia and Pocala cave in Friuli Venezia Giulia.[12]

Description

The short-legged C. l. spelaeus was a glacial mammoth steppe-adapted white wolf. It first appeared 320,000 years ago (MIS 8, Middle Pleistocene), and disappeared along with the mammoth steppe and cave bear fauna at the end of the Late Pleistocene, somewhere between 24,000-12,000 years ago (MIS 2). Compared with the modern day Arctic wolf C. l. arctos and the Siberian Tundra wolf C. l. albus, its legs are shorter than the Tundra wolf but similar to the Arctic wolf and may be its ancestor.[6]

During MIS 8-3 its habitat included the mammoth steppe grasslands and boreal needle forests. It spread across all of Europe through the middle-high elevated mountains, and followed mountain glaciers down to the Mediterranean. This wolf specialized in feeding on cave bear carcasses found inside of caves, and did more damage to its teeth in doing so than any other wolf subspecies.[6]

Its bone proportions are close to those of the Canadian Arctic-boreal mountain-adapted timber wolf and a little larger than those of the modern European wolf. Some postcranial bones have similarly large proportions to those from the Sophie's and Große Teufels Caves,[7] where the bone sizes are closer to those of Scandinavian Arctic and Canadian Columbian wolf subspecies than to those of the smaller European wolves. Bone sizes are one-eighth larger than European wolves, and this wolf was a specialized Late Pleistocene wolf ecomorph.[10]

Diagram of a wolf skull with key features labelled

During the Late Pleistocene, C. l. spelaeus exhibited a changed skeletal development due to the harsh climatic and environmental conditions, and a preference for taking larger prey. This resulted in a larger and more robust wolf with a shortened rostrum, a pronounced development of the temporalis muscles, and proportionally enlarged and wider premolars and carnassials. These features were specialised adaptations for the processing of fast-freezing carcasses associated with the hunting and scavenging of larger prey. Some populations of C. l. spelaeus showed an increase in tooth breakage when compared with the extant C. lupus because they were habitual bone crackers. The large dimensions, robust build and cranio-dental adaptations formed at this time enabled these wolves to hunt larger prey, making the adult Steppe Bison Bison priscus a more attainable target than for their C. lupus relatives.[13]

Adaptation

Cave wolf illustration

Their dens have been identified, with the Zoolithen Cave supporting a large population and has yielded more than 380 bones as well as several skulls (including a holotype). Sophie's Cave has demonstrated the first "Early Late Pleistocene wolf den", with intensive faecal places and the first European record of half-digested cave bear bones found within the faecal areas in the cave. It demonstrates that wolves seem not to have used this cave as a cub-raising den, but that they were cave dwellers that fed on cave bear carcasses, similar to but less so than cave hyenas, but more so than cave lions. The abundant faeces seem to play a role in the "orientation" for trail tracking, similar to modern wolves, and less as den marking. The high abundance in a limited area of the Bear's Passage of the cave might be the result of periodical short-term den use of smaller cave areas. Wolves were scavenging on the bears that hibernated and died there, and therefore a simultaneous use as both a wolf and a cave bear den cannot be expected. Remains of a skeleton of at least one high adult wolf also might have been the result of a battle within the cave with the bears, the same as in the lion taphonomic record.[9]

The ecology of the early to middle Late Pleistocene wolves on the mammoth steppe and the boreal forests is not known, nor is whether they used caves as dens.[9]

Relationship with the dog

Mitochondrial DNA (mDNA) passes along the maternal line and can date back thousands of years.[14] Therefore, phylogenetic analysis of mDNA sequences within a species provides a history of maternal lineages that can be represented as a phylogenetic tree.[15][16]

In 2013, a study analysed the complete and partial mitochondrial genome sequences of 18 fossil canids dated from 1,000 to 36,000 YBP from the Old and New Worlds, and compared these with the complete mitochondrial genome sequences from modern wolves and dogs. Phylogenetic analysis showed that modern dog mDNA haplotypes resolve into four monophyletic clades with strong statistical support, and these have been designated by researchers as clades A-D.[17][18][19] Based on the specimens used in this study, clade A included 64% of the dogs sampled and these were sister to a 14,500 YBP wolf sequence from the Kessleroch cave near Thayngen in the canton of Schaffhausen, Switzerland, with a most recent common ancestor estimated to 32,100 YBP. This group of dogs matched three fossil pre-Columbian New World dogs dated between 1,000 and 8,500 YBP, which supported the hypothesis that pre-Columbian dogs in the New World share ancestry with modern dogs and that they likely arrived with the first humans to the New World. Clade B included 22% of the dog sequences and was related to modern wolves from Sweden and Ukraine, with a common recent ancestor estimated to 9,200 YBP. However, this relationship might represent mitochondrial genome introgression from wolves because dogs were domesticated by this time.

Clade C included 12% of the dogs sampled and these were sister to two ancient dogs from the Bonn-Oberkassel cave (14,700 YBP) and the Kartstein cave (12,500 YBP) near Mechernich in Germany, with a common recent ancestor estimated to 16,000–24,000 YBP. Clade D contained sequences from 2 Scandinavian breeds (Jamthund, Norwegian Elkhound) and were sister to another 14,500 YBP wolf sequence also from the Kesserloch cave, with a common recent ancestor estimated to 18,300 YBP. Its branch is phylogenetically rooted in the same sequence as the "Altai dog" (not a direct ancestor). The data from this study indicated a European origin for dogs that was estimated at 18,800–32,100 years ago based on the genetic relationship of 78% of the sampled dogs with ancient canid specimens found in Europe.[20][17] The data supports the hypothesis that dog domestication preceded the emergence of agriculture[18] and was initiated close to the Last Glacial Maximum when hunter-gatherers preyed on megafauna.[17][21]

The study found that three ancient Belgium canids (the 36,000 YBP "Goyet dog" cataloged as Canis species, along with Belgium 30,000 YBP and 26,000 years YBP cataloged as Canis lupus) formed an ancient clade that was the most divergent group. The study found that the skulls of the "Goyet dog" and the "Altai dog" had some dog-like characteristics and proposed that the may have represented an aborted domestication episode. If so, there may have been originally more than one ancient domestication event for dogs[17] as there was for domestic pigs.[22]

One theory is that domestication occurred during one of the five cold Heinrich events that occurred after the arrival of humans in West Europe 37 000, 29 000, 23 000, 16 500 and 12 000 YBP. The theory is that the extreme cold during one of these events caused humans to either shift their location, adapt through a breakdown in their culture and change of their beliefs, or adopt innovative approaches. The adoption of the large wolf/dog was an adaptation to this hostile environment.[23]

References

  1. ^ Kempe, Stephan; Döppes, Doris (2009). "Cave Bear, Cave Lion and Cave Hyena Skulls from the Public Collection at the Humboldt Museum in Berlin". Acta Carsologica. 38 (2–3). doi:10.3986/ac.v38i2-3.126.
  2. ^ a b Goldfuss, G. A. (1823). "5-Ueber den Hölenwolf (Canis spelaeus) (About the Cave wolf)". Osteologische Beiträge zur Kenntniss verschiedener Säugethiere der Vorwelt (Osteological contributions to different knowledge Beast of the ancients). Vol. 3. Nova Acta Physico-Medica Academiea Caesarae Leopoldino-Carolinae Naturae Curiosorum. pp. 451–455.
  3. ^ a b Kuzmina, I. E.; Sablin, M. V. (1994). "Wolf Canis lupus L. from the Late Paleolithic sites Kostenki on the Don River". Trudy Zoologicheskogo Instituta (in Russian) (256): 44–58. See the last page for the summary in English
  4. ^ a b c Boudadi-Maligne, Myriam (2012). "Une nouvelle sous-espèce de loup (Canis lupus maximus nov. Subsp.) dans le Pléistocène supérieur d'Europe occidentale [A new subspecies of wolf (Canis lupus maximus nov. subsp.) from the upper Pleistocene of Western Europe]". Comptes Rendus Palevol. 11 (7): 475. doi:10.1016/j.crpv.2012.04.003.
  5. ^ a b c Baryshnikov, Gennady F.; Mol, Dick; Tikhonov, Alexei N (2009). "Finding of the Late Pleistocene carnivores in Taimyr Peninsula (Russia, Siberia) with paleoecological context". Russian Journal of Theriology. 8 (2): 107–113. doi:10.15298/rusjtheriol.08.2.04. Retrieved September 7, 2022.
  6. ^ a b c d e f g h Cajus G. Dietrich (2022). "Eurasian Grey and White wolf ancestors—800,000 years evolution, adaptation, pathologies and European dog origins". Acta Zoologica. 105 (1). Wiley: 2–37. doi:10.1111/azo.12451.
  7. ^ a b Diedrich 2015, pp. 96–99
  8. ^ Diedrich 2017, pp. 108–118
  9. ^ a b c d Diedrich, C. G. (2013). "Extinctions of Late Ice Age Cave Bears as a Result of Climate/Habitat Change and Large Carnivore Lion/Hyena/Wolf Predation Stress in Europe". ISRN Zoology. 2013: 1–25. doi:10.1155/2013/138319.
  10. ^ a b Diedrich 2015, pp. 137
  11. ^ Jánossy, Dénes (2012). "Vertebrate faunas of the Middle Pleistocene of Hungary". Pleistocene Vertebrate Faunas of Hungary. Elsevier Science. p. 102. ISBN 978-0444556356.
  12. ^ Berte, E.; Pandolfi, L. (2014). "Canis lupus (Mammalia, Canidae) from the Late Pleistocene deposit of Avetrana (Taranto, Southern Italy)". Rivista Italiana di Paleontoligia e Stratigrafia. 120 (3): 367–379.
  13. ^ Marciszak, Adrian (2023). "History of Polish Canidae (Carnivora, Mammalia) and Their Biochronological Implications on the Eurasian Background". Genes (journal). MDPI. doi:10.3390/genes14030539.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  14. ^ Arora, Devender; Singh, Ajeet; Sharma, Vikrant; Bhaduria, Harvendra Singh; Patel, Ram Bahadur (2015). "Hgs Db: Haplogroups Database to understand migration and molecular risk assessment". Bioinformation. 11 (6): 272–275. doi:10.6026/97320630011272. PMC 4512000. PMID 26229286.
  15. ^ Avise, J. C. (1994). Molecular Markers, Natural History, and Evolution. Chapman & Hall. pp. 109–110. ISBN 978-0-412-03781-8.
  16. ^ Robert K. Wayne; Jennifer A. Leonard; Carles Vila (2006). "Chapter 19:Genetic Analysis of Dog Domestication". In Melinda A. Zeder (ed.). Documenting Domestication:New Genetic and Archaeological Paradigms. University of California Press. pp. 279–295. ISBN 978-0-520-24638-6.
  17. ^ a b c d Thalmann O, Shapiro B, Cui P, Schuenemann VJ, Sawyer SK, Greenfield DL, Germonpre MB, Sablin MV, Lopez-Giraldez F, Domingo-Roura X, Napierala H, Uerpmann HP, Loponte DM, Acosta AA, Giemsch L, Schmitz RW, Worthington B, Buikstra JE, Druzhkova A, Graphodatsky AS, Ovodov ND, Wahlberg N, Freedman AH, Schweizer RM, Koepfli KP, Leonard JA, Meyer M, Krause J, Paabo S, Green RE, Wayne RK (2013). "Complete Mitochondrial Genomes of Ancient Canids Suggest a European Origin of Domestic Dogs". Science. 342 (6160): 871–874. Bibcode:2013Sci...342..871T. doi:10.1126/science.1243650. PMID 24233726. S2CID 1526260.
  18. ^ a b Vila, C. (1997). "Multiple and ancient origins of the domestic dog". Science. 276 (5319): 1687–1689. doi:10.1126/science.276.5319.1687. PMID 9180076.
  19. ^ Bjornerfeldt, S (2006). "Relaxation of selective constraint on dog mitochondrial DNA followed domestication". Genome Research. 16 (8): 990–994. doi:10.1101/gr.5117706. PMC 1524871. PMID 16809672.
  20. ^ Miklosi, Adam (2018). "1-Evolution & Ecology". The Dog: A Natural History. Princeton University Press. pp. 13–39. ISBN 978-0-691-17693-2.
  21. ^ Shipman, P. (2015). The Invaders:How humans and their dogs drove Neanderthals to extinction. Harvard University Press. p. 149. ISBN 9780674736764.
  22. ^ Frantz, L. (2015). "Evidence of long-term gene flow and selection during domestication from analyses of Eurasian wild and domestic pig genomes". Nature Genetics. 47 (10): 1141–1148. doi:10.1038/ng.3394. PMID 26323058. S2CID 205350534.
  23. ^ Schnitzler, Annick; Patou-Mathis, Marylène (2017). "Wolf (Canis lupus Linnaeus, 1758) domestication: Why did it occur so late and at such high latitude? A hypothesis". Anthropozoologica. 52 (2): 149. doi:10.5252/az2017n2a1. S2CID 134153466.

Bibliography

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