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Multituberculata

Multituberculata (commonly known as multituberculates, named for the multiple tubercles of their teeth) is an extinct order of rodent-like mammals with a fossil record spanning over 130 million years. They first appeared in the Middle Jurassic, and reached a peak diversity during the Late Cretaceous and Paleocene. They eventually declined from the mid-Paleocene onwards, disappearing from the known fossil record in the late Eocene.[1] They are the most diverse order of Mesozoic mammals with more than 200 species known, ranging from mouse-sized to beaver-sized. These species occupied a diversity of ecological niches, ranging from burrow-dwelling to squirrel-like arborealism to jerboa-like hoppers.[2][3] Multituberculates are usually placed as crown mammals outside either of the two main groups of living mammals—Theria, including placentals and marsupials, and Monotremata[4]—but usually as closer to Theria than to monotremes.[5][6] They are considered to be closely related to Euharamiyida and Gondwanatheria as part of Allotheria.

Multituberculates
Skeleton of Catopsbaatar
Scientific classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Infraclass: Allotheria
Order: Multituberculata
Cope, 1884
Suborders

Description edit

 
Restoration of Taeniolabis, the largest multituberculate at approximately 22 kg (49 lb).

The multituberculates had a cranial and dental anatomy superficially similar to rodents such as mice and rats, with cheek-teeth separated from the chisel-like front teeth by a wide tooth-less gap (the diasteme). Each cheek-tooth displayed several rows of small cusps (or tubercles, hence the name) that operated against similar rows in the teeth of the jaw; the exact homology of these cusps to therian ones is still a matter of debate.[citation needed] Unlike rodents, which have ever-growing teeth, multituberculates underwent dental replacement patterns typical to most mammals (though in at least some species the lower incisors continued to erupt long after the root's closure).[7] Multituberculates are notable for the presence of a massive fourth lower premolar, the plagiaulacoid; other mammals, like Plesiadapiformes and diprotodontian marsupials, also have similar premolars in both upper and lower jaws, but in multituberculates this tooth is massive and the upper premolars are not modified this way. In basal multituberculates all three lower premolars were plagiaulacoids, increasing in size posteriorly, but in Cimolodonta only the fourth lower premolar remained, with the third one remaining only as a vestigial peg-like tooth,[7] and in several taxa like taeniolabidoideans, the plagiaulacoid disappeared entirely or was reconverted into a molariform tooth.[8][9][10]

 
Skull of Ptilodus. Notice the massive blade-like lower premolar.

Unlike rodents and similar therians, multituberculates had a palinal jaw stroke (front-to-back), instead of a propalinal (back-to-front) or transverse (side-to-side) one; as a consequence, their jaw musculature and cusp orientation is radically different.[4][7] Palinal jaw strokes are almost entirely absent in modern mammals (with the possible exception of the dugong[11]), but are also present in haramiyidans, argyrolagoideans and tritylodontids, the former historically united with multituberculates on that basis. Multituberculate mastication is thought to have operated in a two stroke cycle: first, food held in place by the last upper premolar was sliced by the bladelike lower pre-molars as the dentary moved orthally (upward). Then the lower jaw moved palinally, grinding the food between the molar cusp rows.[4][7]

 
Lower jaws and teeth of allodontid multituberculates

The structure of the pelvis in the Multituberculata suggests that they gave birth to tiny helpless, underdeveloped young, similar to modern marsupials, such as kangaroos.[2][7] However, a 2022 study reveals that they might actually have had long gestation periods like placentals.[12]

At least two lineages developed hypsodonty, in which tooth enamel extends beyond the gumline: lambdopsalid taeniolabidoideans[13] and sudamericid gondwanatheres.[14]

Studies published in 2018 demonstrated that multituberculates had relatively complex brains, some braincase regions even absent in therian mammals.[15]

Evolution edit

Multituberculates first appear in the fossil record during the Jurassic period, and then survived and even dominated for over one hundred million years, longer than any other order of mammaliforms, including placental mammals. The earliest known multituberculates are from the Middle Jurassic (Bathonian ~166-168 million years ago) of England and Russia, including Hahnotherium and Kermackodon from the Forest Marble Formation of England, and Tashtykia and Tagaria from the Itat Formation of Russia. These forms are only known from isolated teeth, which bear close similarity to those of euharamyidans, which they are suspected to be closely related.[16] During the Late Jurassic and Early Cretaceous, primitive multituberculates, collectively grouped into the paraphyletic "Plagiaulacida" were abundant and widespread across Laurasia (including Europe, Asia and North America). During the Aptian stage of the Early Cretaceous, the advanced subgroup Cimolodonta appeared in North America, characterised by a reduced number of lower premolars, with a blade-like lower fourth premolar. By the early Late Cretaceous (Cenomanian) Cimolodonta had replaced all other multituberculate lineages.[17]

During the Late Cretaceous, multituberculates experienced an adaptive radiation, corresponding with a shift towards herbivory.[18] Multituberculates reached their peak diversity during the early Paleocene, shortly after the Cretaceous–Paleogene extinction event, but declined from the mid Paleocene onwards, likely due to competition with placental mammals such as rodents and ungulates, the group finally became extinct in the Late Eocene.[19][20] There are some isolated records of multituberculates from the Southern Hemisphere, including the cimolodontan Corriebaatar from the Early Cretaceous of Australia,[21] and fragmentary remains from the Late Cretaceous Maevarano Formation of Madagascar.[22] The family Ferugliotheriidae from the Late Cretaceous of South America, traditionally considered gondwanatherians, may actually be cimolodontan multituberculates.[21]

During the Late Cretaceous and Paleocene the multituberculates radiated into a wide variety of morphotypes, including the squirrel-like arboreal ptilodonts. The peculiar shape of their last lower premolar is their most outstanding feature. These teeth were larger and more elongated than the other cheek-teeth and had an occlusive surface forming a serrated slicing blade. Though it can be assumed that this was used for crushing seeds and nuts, it is believed that most small multituberculates also supplemented their diet with insects, worms, and fruits.[4] Tooth marks attributed to multituberculates are known on Champsosaurus fossils, indicating that at least some of these mammals were scavengers.[23] A ptilodont that thrived in North America was Ptilodus. Thanks to the well-preserved Ptilodus specimens found in the Bighorn Basin, Wyoming, we know that these multituberculates were able to abduct and adduct their big toes, and thus that their foot mobility was similar to that of modern squirrels, which descend trees head first.[4]

 
Restoration of Catopsbaatar

Another group of multituberculates, the taeniolabids, were heavier and more massively built, indicating that they lived a fully terrestrial life. The largest specimens weighed probably as much as 22 kg (49 lb), making them comparable in size to large rodents like the modern beaver.[24][25]

Classification edit

Multituberculate is generally placed in the Allotheria alongside Euharamiyida, a clade of mammals known from the Middle Jurassic to Early Cretaceous of the Asia and possibly Europe that several morphological similarities to multituberculates.[16][26]

Gondwanatheria is a monophyletic group of allotherians that was diverse in the Late Cretaceous of South America, India, Madagascar and possibly Africa and occurs onwards into the Paleogene of South America and Antarctica. Their placement within Allotheria is highly controversial, with some phylogenies recovering the group as deeply nested within multituberculates, while others recover them as a distinct branch of allotherians separate from multituberculates.[26]

 
Restoration of Taeniolabis taoensis

In their 2001 study, Kielan-Jaworowska and Hurum found that most multituberculates could be referred to two suborders: "Plagiaulacida" and Cimolodonta. The exception is the genus Arginbaatar, which shares characteristics with both groups.

"Plagiaulacida" is paraphyletic, representing the more primitive evolutionary grade. Its members are the more basal Multituberculata. Chronologically, they ranged from perhaps the Middle Jurassic until the mid-Cretaceous. This group is further subdivided into three informal groupings: the allodontid line, the paulchoffatiid line, and the plagiaulacid line.

Cimolodonta is, apparently, a natural (monophyletic) suborder. This includes the more derived Multituberculata, which have been identified from the lower Cretaceous to the Eocene. The superfamilies Djadochtatherioidea, Taeniolabidoidea, Ptilodontoidea are recognized, as is the Paracimexomys group. Additionally, there are the families Cimolomyidae, Boffiidae, Eucosmodontidae, Kogaionidae, Microcosmodontidae and the two genera Uzbekbaatar and Viridomys. More precise placement of these types awaits further discoveries and analysis.[27][better source needed]

Taxonomy edit

Subgroups
 
Multituberculate phylogenetic tree[28]

Based on the combined works of Mikko's Phylogeny Archive[29] and Paleofile.com.[citation needed]

Suborder †Plagiaulacida Simpson 1925

Plagiaulacoidea
  • Suborder †Cimolodonta McKenna, 1975
    • Genus ?†Allocodon non Marsh, 1881
      • Species †A. fortis Marsh, 1889
      • Species †A. lentus Marsh, 1892 [Cimolomys lentus]
      • Species †A. pumilis Marsh, 1892 [Cimolomys pumilus]
      • Species †A. rarus Marsh, 1889
    • Genus ?†Ameribaatar Eaton & Cifelli, 2001
    • Genus ?†Bubodens Wilson, 1987
      • Species †Bubodens magnus Wilson, 1987
    • Genus ?†Clemensodon Krause, 1992
    • Genus ?†Fractinus Higgins 2003
      • Species †Fractinus palmorum Higgins, 2003
    • Genus ?†Uzbekbaatar Kielan-Jaworowska & Nesov, 1992
    • Genus ?†Viridomys Fox 1971
    • Family †Corriebaataridae Rich et al., 2009
    • Paracimexomys group
      • Genus Paracimexomys Archibald, 1982
        • Species? †P. crossi Cifelli, 1997
        • Species? †P. dacicus Grigorescu & Hahn, 1989
        • Species? †P. oardaensis (Codrea et al., 2014) [Barbatodon oardaensis Codrea et al., 2014]
        • Species †P. magnus (Sahni, 1972) Archibald, 1982 [Cimexomys magnus Sahni, 1972]
        • Species †P. magister (Fox, 1971) Archibald, 1982 [Cimexomys magister Fox, 1971]
        • Species †P. perplexus Eaton & Cifelli, 2001
        • Species †P. robisoni Eaton & Nelson, 1991
        • Species †P. priscus (Lillegraven, 1969) Archibald, 1982 [Cimexomys priscus Lillegraven, 1969; genotype Paracimexomys sensu Eaton & Cifelli, 2001]
        • Species †P. propriscus Hunter, Heinrich & Weishampel 2010
      • Genus Cimexomys Sloan & Van Valen, 1965
        • Species †C. antiquus Fox, 1971
        • Species †C. gregoryi Eaton, 1993
        • Species †C. judithae Sahni, 1972 [Paracimexomys judithae (Sahni, 1972) Archibald, 1982]
        • Species †C. arapahoensis Middleton & Dewar, 2004
        • Species †C. minor Sloan & Van Valen, 1965
        • Species? †C. gratus (Jepson, 1930) Lofgren, 1995 [Cimexomys hausoi Archibald, 1983; Eucosmodon gratus Jepson, 1930; Mesodma ambigua? Jepson, 1940; Stygimus gratus Jepson, 1930]
      • Genus †Bryceomys Eaton, 1995
      • Genus †Cedaromys Eaton & Cifelli, 2001
        • Species †C. bestia (Eaton & Nelson, 1991) Eaton & Cifelli, 2001 [Paracimexomys bestia Eaton & Nelson, 1991]
        • Species †C. hutchisoni Eaton 2002
        • Species †C. minimus Eaton 2009
        • Species †C. parvus Eaton & Cifelli, 2001
      • Genus †Dakotamys Eaton, 1995
        • Species? †D. sp. Eaton, 1995
        • Species †D. malcolmi Eaton, 1995
        • Species †D. shakespeari Eaton 2013
    • Family †Boffidae Hahn & Hahn, 1983 sensu Kielan-Jaworowska & Hurum 2001
      • Genus †Boffius Vianey-Liaud, 1979
        • Species †Boffius splendidus Vianey-Liaud, 1979 [Boffiidae Hahn & Hahn, 1983 sensu Kielan-Jaworowska & Hurum, 2001]
    • Family †Cimolomyidae Marsh, 1889 sensu Kielan-Jaworowska & Hurum, 2001
      • Genus †Paressodon Wilson, Dechense & Anderson, 2010
        • Species †Paressodon nelsoni Wilson, Dechense & Anderson, 2010
      • Genus †Cimolomys Marsh, 1889 [?Allacodon Marsh, 1889; Selenacodon Marsh, 1889]
        • Species †C. clarki Sahni, 1972
        • Species †C. gracilis Marsh, 1889 [Cimolomys digona Marsh, 1889; Meniscoessus brevis; Ptilodus gracilis Osborn, 1893 non Gidley 1909; Selenacodon brevis Marsh, 1889]
        • Species †C. trochuus Lillegraven, 1969
        • Species †C. milliensis Eaton, 1993a
        • Species ?†C. bellus Marsh, 1889
      • Genus ?†Essonodon Simpson, 1927
        • Species †E. browni Simpson, 1927 [cimolodontidae? Kielan-Jaworowska & Hurum 2001]
      • Genus ?†Buginbaatar Kielan-Jaworowska & Sochava, 1969
      • Genus ?†Meniscoessus Cope, 1882 [Dipriodon Marsh, 1889; Tripriodon Marsh, 1889 nomen dubium; Triprotodon Chure & McIntosh, 1989 nomen dubium; Selenacodon Marsh, 1889, Halodon Marsh, 1889, Oracodon Marsh, 1889]
        • Species †M. caperatus Marsh, 1889
        • Species †M. collomensis Lillegraven, 1987
        • Species †M. conquistus Cope 1882
        • Species †M. ferox Fox, 1971a
        • Species †M. intermedius Fox, 1976b
        • Species †M. major (Russell, 1936) [Cimolomys major Russell 1937]
        • Species †M. robustus (Marsh, 1889) [Dipriodon robustus Marsh 1889; Dipriodon lacunatus Marsh, 1889; Tripriodon coelatus Marsh, 1889; Meniscoessus coelatus Marsh, 1889; Selenacodon fragilis Marsh, 1889; Meniscoessus fragilis Marsh, 1889; Halodon sculptus (Marsh, 1889); Cimolomys sculptus Marsh, 1889; Meniscoessus sculptus Marsh, 1889; Oracodon anceps Marsh, 1889; Oracodon conulus Marsh, 1892; Meniscoessus borealis Simpson, 1927c; Meniscoessus greeni Wilson, 1987]
        • Species †M. seminoensis Eberle & Lillegraven, 1998a
    • Family †Kogaionidae Rãdulescu & Samson, 1996
    • Family †Eucosmodontidae Jepsen, 1940 sensu Kielan-Jaworowska & Hurum, 2001 [Eucosmodontidae: Eucosmodontinae Jepsen, 1940 sensu McKenna & Bell, 1997]
    • Family †Microcosmodontidae Holtzman & Wolberg, 1977 [Eucosmodontidae: Microcosmodontinae Holtzman & Wolberg, 1977 sensu McKenna & Bell, 1997]
    • Superfamily †Ptilodontoidea Cope, 1887 sensu McKenna & Bell, 1997 e Kielan-Jaworowska & Hurum, 2001
      • Family †Cimolodontidae Marsh, 1889 sensu Kielan-Jaworowska & Hurum, 2001
        • Genus †Liotomus Lemoine, 1882 [Neoctenacodon Lemoine 1891]
          • Species? †L. marshi (Lemoine, 1882) Cope, 1884 [Neoctenacodon marshi Lemoine, 1882; Neoplagiaulax marshi (Lemoine 1882); Plagiaulax marshi (Lemoine 1882)] [Eucosmodontidae? McKenna & Bell, 1997]
        • Genus †Yubaatar Xu et al., 2015
        • Genus †Anconodon Jepsen, 1940
          • Species? †A. lewisi (Simpson 1935) Sloan, 1987
          • Species †A. gibleyi (Simpson, 1935) [Ptilodus gidleyi Simpson, 1935]
          • Species †A. cochranensis (Russell, 1929) [Liotomus russelli (Simpson, 1935); Anconodon russelli (Simpson, 1935) Sloan, 1987; Ectopodon cochranensis (Russell, 1967)]
        • Genus †Cimolodon Marsh, 1889 [Nanomys Marsh, 1889, Nanomyops Marsh, 1892]
          • Species †C. agilis Marsh, 1889
          • Species †C. foxi Eaton, 2002
          • Species †C. gracilis Marsh, 1889
          • Species †C. electus Fox, 1971
          • Species †C. nitidus Marsh, 1889 [Allacodon rarus Marsh, 1892 sensu Clemens, 1964a; Nanomys minutus Marsh, 1889; Nanomyops minutus (Marsh, 1889) Marsh, 1892; Halodon serratus Marsh, 1889; Ptilodus serratus (Marsh, 1889) Gidley 1909]
          • Species †C. parvus Marsh, 1889
          • Species †C. peregrinus Donohue, Wilson & Breithaupt, 2013
          • Species †C. similis Fox, 1971
          • Species †C. wardi Eaton, 2006
      • Family Incertae sedis
      • Family †Neoplagiaulacidae Ameghino, 1890 [Ptilodontidae: Neoplagiaulacinae Ameghino, 1890 sensu McKenna & Bell, 1997]
      • Family †Ptilodontidae Cope, 1887 [Ptilodontidae: Ptilodontinae Cope, 1887 sensu McKenna & Bell, 1997]
        • Genus †Kimbetohia Simpson, 1936
          • Species †K. cambi [Granger, Gregory & Colbert in Matthew, 1937, or Simpson, 1936]
          • Species †K. sp. cf. K. cambi
        • Genus †Ptilodus Cope, 1881 [Chirox Cope, 1884]
          • Species? †P. fractus
          • Species †P. kummae Krause, 1977
          • Species †P. gnomus Scott, Fox & Youzwyshyn, 2002 [cf. Ectypodus hazeni (Jepsen, 1940) Gazin, 1956]
          • Species †P. mediaevus Cope, 1881 [Ptilodus plicatus (Cope, 1884); Chirox plicatus Cope, 1884 P. ferronensis Gazin, 1941]
          • Species †P. montanus Douglass, 1908 [P. gracilis Gidley, 1909; P. admiralis Hay, 1930]
          • Species †P. tsosiensis Sloan, 1981
          • Species †P. wyomingensis Jepsen, 1940
        • Genus †Baiotomeus Krause, 1987
        • Genus †Prochetodon Jepsen, 1940
          • Species †P. cavus Jespen, 1940
          • Species †P. foxi Krause, 1987
          • Species †P. taxus Krause, 1987
          • Species? †P. speirsae Scott, 2004
    • Superfamily †Taeniolabidoidea Granger & Simpson, 1929 sensu Kielan-Jaworowska & Hurum, 2001
    • Superfamily †Djadochtatherioidea Kielan-Jaworowska & Hurum, 1997 sensu Kielan-Jaworowska & Hurum, 2001[Djadochtatheria Kielan-Jaworowska & Hurum, 1997]

Phylogeny[28] edit

Paleoecology edit

Behaviour edit

Multituberculates are some of the earliest mammals to display complex social behaviours. One species, Filikomys, from the Late Cretaceous of North America, engaged in multi-generational group nesting and burrowing.[30]

Extinction edit

The extinction of multituberculates has been a topic of controversy for several decades.[31] After at least 88 million years of dominance over most mammalian assemblies, multituberculates reached the peak of their diversity in the early Palaeocene, before gradually declining across the final stages of the epoch and the Eocene, finally disappearing in the early Oligocene.[32]

The last multituberculate species, Ectypodus childei, went extinct near the end of the Eocene in North America. It is unclear why this particular species persisted for so long when all of its counterparts succumbed to replacement by rodents.[33]: 43 

Traditionally, the extinction of multituberculates has been linked to the rise of rodents (and, to a lesser degree, earlier placental competitors like hyopsodonts and Plesiadapiformes), which supposedly competitively excluded multituberculates from most mammalian faunas.[1]

However, the idea that multituberculates were replaced by rodents and other placentals has been criticised by several authors. For one thing, it relies on the assumption that these mammals are "inferior" to more derived placentals, and ignores the fact that rodents and multituberculates had co-existed for at least 15 million years. According to some researchers, multituberculate "decline" is shaped by sharp extinction events, most notably after the Tiffanian, where a sudden drop in diversity occurs. Finally, the youngest known multituberculates do not exemplify patterns of competitive exclusion; the Oligocene Ectypodus is a rather generalistic species, rather than a specialist. This combination of factors suggests that, rather than gradually declining due to pressure from rodents and similar placentals, multituberculates simply could not cope with climatic and vegetation changes, as well as the rise of new predatory eutherians, such as miacids.[32]

More recent studies show a mixed effect. Multituberculate faunas in North America and Europe do indeed decline in correlation to the introduction of rodents in these areas. However, Asian multituberculate faunas co-existed with rodents with minimal extinction events, implying that competition was not the main cause for the extinction of Asiatic multituberculates. As a whole, it seems that Asian multituberculates, unlike North American and European species, never recovered from the KT event, which allowed the evolution and propagation of rodents in the first place.[31] A recent study seems to indeed indicate that eutherians recovered more quickly from the KT event than multituberculates.[34] Conversely, another study has shown that placental radiation did not start significantly until after the decline of multituberculates.[20]

References edit

  1. ^ a b Krause, David W. (1986). "Competitive exclusion and taxonomic displacement in the fossil record". Vertebrates, Phylogeny, and Philosophy. pp. 95–117. doi:10.2113/gsrocky.24.special_paper_3.95. ISBN 978-0-941570-02-2.
  2. ^ a b Weil, Anne (June 1997). "Introduction to Multituberculates: The 'Lost Tribe' of Mammals". Berkeley: UCMP.
  3. ^ Chen, Meng; Philip Wilson, Gregory (2015). "A multivariate approach to infer locomotor modes in Mesozoic mammals". Paleobiology. 41 (2): 280–312. Bibcode:2015Pbio...41..280C. doi:10.1017/pab.2014.14. S2CID 86087687.
  4. ^ a b c d e Agustí-Antón 2002, pp 3-4
  5. ^ Benton, Michael J. Vertebrate Palaeontology (2004), p. 300
  6. ^ Carrano, Matthew T., and Richard W. Blob, Timothy J. Gaudin, and John R. Wible (2006). Amniote Paleobiology: Perspectives on the Evolution of Mammals, Birds, and Reptiles, p. 358.
  7. ^ a b c d e Kielan-Jaworowska, Zofia, Richard L. Cifelli, and Zhe-Xi Luo (2005). Mammals from the Age of Dinosaurs: Origins, Evolution, and Structure , p. 299
  8. ^ Gurovich 2005 p. 334[full citation needed]
  9. ^ Gurovich, Yamila; Beck, Robin (March 2009). "The Phylogenetic Affinities of the Enigmatic Mammalian Clade Gondwanatheria". Journal of Mammalian Evolution. 16 (1): 25–49. doi:10.1007/s10914-008-9097-3. S2CID 42799370.
  10. ^ Rougier et al. 2009 p.233[full citation needed]
  11. ^ Lanyon, J. M.; Sanson, G. D. (February 2006). "Degenerate dentition of the dugong (Dugong dugon), or why a grazer does not need teeth: morphology, occlusion and wear of mouthparts". Journal of Zoology. 268 (2): 133–152. doi:10.1111/j.1469-7998.2005.00004.x.
  12. ^ "New study challenges old views on what's 'primitive' in mammalian reproduction". 25 July 2022.
  13. ^ Williamson, Thomas E.; Brusatte, Stephen L.; Secord, Ross; Shelley, Sarah (2015). "A new taeniolabidoid multituberculate (Mammalia) from the middle Puercan of the Nacimiento Formation, New Mexico, and a revision of taeniolabidoid systematics and phylogeny". Zoological Journal of the Linnean Society. 177: 183–208. doi:10.1111/zoj.12336.
  14. ^ "Gondwanatheria".[dead link]
  15. ^ Crompton, A. W.; Musinsky, C.; Rougier, G. W.; Bhullar, B.-A. S.; Miyamae, J. A. (September 2018). "Origin of the Lateral Wall of the Mammalian Skull: Fossils, Monotremes and Therians Revisited". Journal of Mammalian Evolution. 25 (3): 301–313. doi:10.1007/s10914-017-9388-7. S2CID 16072755.
  16. ^ a b Averianov, Alexander O.; Martin, Thomas; Lopatin, Alexey V.; Schultz, Julia A.; Schellhorn, Rico; Krasnolutskii, Sergei; Skutschas, Pavel; Ivantsov, Stepan (May 2021). "Multituberculate mammals from the Middle Jurassic of Western Siberia, Russia, and the origin of Multituberculata". Papers in Palaeontology. 7 (2): 769–787. doi:10.1002/spp2.1317. ISSN 2056-2799. S2CID 219067218.
  17. ^ Weaver, Lucas N.; Wilson, Gregory P.; Krumenacker, L. J.; Mclaughlin, Kayla; Moore, Jason R.; Varricchio, David J. (2019-03-04). "New multituberculate mammals from the mid-Cretaceous (lower Cenomanian) Wayan Formation of southeastern Idaho and implications for the early evolution of Cimolodonta". Journal of Vertebrate Paleontology. 39 (2): e1604532. Bibcode:2019JVPal..39E4532W. doi:10.1080/02724634.2019.1604532. ISSN 0272-4634. S2CID 196655261.
  18. ^ Wilson, Gregory P.; Evans, Alistair R.; Corfe, Ian J.; Smits, Peter D.; Fortelius, Mikael; Jernvall, Jukka (March 2012). "Adaptive radiation of multituberculate mammals before the extinction of dinosaurs". Nature. 483 (7390): 457–460. Bibcode:2012Natur.483..457W. doi:10.1038/nature10880. ISSN 1476-4687. PMID 22419156. S2CID 4419772.
  19. ^ Adams, Neil F.; Rayfield, Emily J.; Cox, Philip G.; Cobb, Samuel N.; Corfe, Ian J. (March 2019). "Functional tests of the competitive exclusion hypothesis for multituberculate extinction". Royal Society Open Science. 6 (3): 181536. Bibcode:2019RSOS....681536A. doi:10.1098/rsos.181536. ISSN 2054-5703. PMC 6458384. PMID 31032010.
  20. ^ a b Brocklehurst, Neil; Panciroli, Elsa; Benevento, Gemma Louise; Benson, Roger B. J. (July 2021). "Mammaliaform extinctions as a driver of the morphological radiation of Cenozoic mammals". Current Biology. 31 (13): 2955–2963.e4. doi:10.1016/j.cub.2021.04.044. PMID 34004143. S2CID 234782605.
  21. ^ a b Rich, Thomas; Trusler, Peter; Kool, Lesley; White, Matt A.; Bevitt, Joseph; Morton, Steven; Vickers−Rich, Patricia (2022). "Second specimen of Corriebaatar marywaltersae from the Lower Cretaceous of Australia confirms its multituberculate affinities". Acta Palaeontologica Polonica. 67. doi:10.4202/app.00924.2021. ISSN 0567-7920. S2CID 247905998.
  22. ^ Krause, David W.; Hoffmann, Simone; Werning, Sarah (December 2017). "First postcranial remains of Multituberculata (Allotheria, Mammalia) from Gondwana". Cretaceous Research. 80: 91–100. Bibcode:2017CrRes..80...91K. doi:10.1016/j.cretres.2017.08.009.
  23. ^ Longrich, Nicholas R.; Ryan, Michael J. (2010). "Mammalian tooth marks on the bones of dinosaurs and other Late Cretaceous vertebrates". Palaeontology. 53 (4): 703–709. Bibcode:2010Palgy..53..703L. doi:10.1111/j.1475-4983.2010.00957.x.
  24. ^ Krause et al 2021
  25. ^ Wilson et al 2012
  26. ^ a b Hoffmann, Simone; Beck, Robin M. D.; Wible, John R.; Rougier, Guillermo W.; Krause, David W. (2020-12-14). "Phylogenetic placement of Adalatherium hui (Mammalia, Gondwanatheria) from the Late Cretaceous of Madagascar: implications for allotherian relationships". Journal of Vertebrate Paleontology. 40 (sup1): 213–234. Bibcode:2020JVPal..40S.213H. doi:10.1080/02724634.2020.1801706. ISSN 0272-4634. S2CID 230968231.
  27. ^ Dykes Multituberculata (Cope 1884)
  28. ^ a b Nicolás R. Chimento; Federico L. Agnolin; Fernando E. Novas (2015). "The bizarre 'metatherians' Groeberia and Patagonia, late surviving members of gondwanatherian mammals". Historical Biology: An International Journal of Paleobiology. 27 (5): 603–623. doi:10.1080/08912963.2014.903945. hdl:11336/85076. S2CID 216591096.
  29. ^ Mikko's Phylogeny Archive Haaramo, Mikko (2007). "Mammaliaformes – mammals and near-mammals". Retrieved 30 December 2015.
  30. ^ Weaver, Lucas N.; Varricchio, David J.; Sargis, Eric J.; Chen, Meng; Freimuth, William J.; Wilson Mantilla, Gregory P. (2 November 2020). "Early mammalian social behaviour revealed by multituberculates from a dinosaur nesting site". Nature Ecology & Evolution. 5 (1): 32–37. doi:10.1038/s41559-020-01325-8. PMID 33139921. S2CID 226241443.
  31. ^ a b Wood, D. Joseph (2010). (M.S.). The Ohio State University. Archived from the original on 2015-04-08. Retrieved 2015-04-03.
  32. ^ a b Ostrander, Gregg (1 January 1984). "The Early Oligocene (Chadronian) Raben Ranch Local Fauna, Northwest Nebraska: Multituberculata; with Comments on the Extinction of the Allotheria". Transactions of the Nebraska Academy of Sciences and Affiliated Societies.
  33. ^ Wood, D. Joseph (2010). (Thesis). The Ohio State University. Archived from the original on 2023-05-19. Retrieved 2023-05-19.
  34. ^ Pires, Mathias M.; Rankin, Brian D.; Silvestro, Daniele; Quental, Tiago B. (1804). "Diversification dynamics of mammalian clades during the K–Pg mass extinction". Biology Letters. 14 (9): 2058. doi:10.1098/rsbl.2018.0458. PMC 6170748. PMID 30258031.

Sources edit

  • Agustí, Jordi; Antón, Mauricio (2002). Mammoths, Sabertooths, and Hominids: 65 Millions Years of Mammalian Evolution in Europe. New York: Columbia University Press. ISBN 978-0-231-11640-4.
  • Dykes, Trevor. . Archived from the original on December 28, 2009.
  • Kielan-Jaworowska, Zofia; Hurum, Jørn H. (2001). "Phylogeny and Systematics of multituberculate mammals" (PDF). Palaeontology. 44 (3): 389–429. Bibcode:2001Palgy..44..389K. doi:10.1111/1475-4983.00185. S2CID 83592270.

multituberculata, commonly, known, multituberculates, named, multiple, tubercles, their, teeth, extinct, order, rodent, like, mammals, with, fossil, record, spanning, over, million, years, they, first, appeared, middle, jurassic, reached, peak, diversity, duri. Multituberculata commonly known as multituberculates named for the multiple tubercles of their teeth is an extinct order of rodent like mammals with a fossil record spanning over 130 million years They first appeared in the Middle Jurassic and reached a peak diversity during the Late Cretaceous and Paleocene They eventually declined from the mid Paleocene onwards disappearing from the known fossil record in the late Eocene 1 They are the most diverse order of Mesozoic mammals with more than 200 species known ranging from mouse sized to beaver sized These species occupied a diversity of ecological niches ranging from burrow dwelling to squirrel like arborealism to jerboa like hoppers 2 3 Multituberculates are usually placed as crown mammals outside either of the two main groups of living mammals Theria including placentals and marsupials and Monotremata 4 but usually as closer to Theria than to monotremes 5 6 They are considered to be closely related to Euharamiyida and Gondwanatheria as part of Allotheria MultituberculatesTemporal range Middle Jurassic Late Eocene PreꞒ Ꞓ O S D C P T J K Pg NSkeleton of CatopsbaatarScientific classificationDomain EukaryotaKingdom AnimaliaPhylum ChordataClass MammaliaInfraclass AllotheriaOrder MultituberculataCope 1884Suborders Plagiaulacida paraphyletic Cimolodonta Contents 1 Description 2 Evolution 3 Classification 3 1 Taxonomy 3 2 Phylogeny 28 4 Paleoecology 4 1 Behaviour 4 2 Extinction 5 References 6 SourcesDescription edit nbsp Restoration of Taeniolabis the largest multituberculate at approximately 22 kg 49 lb The multituberculates had a cranial and dental anatomy superficially similar to rodents such as mice and rats with cheek teeth separated from the chisel like front teeth by a wide tooth less gap the diasteme Each cheek tooth displayed several rows of small cusps or tubercles hence the name that operated against similar rows in the teeth of the jaw the exact homology of these cusps to therian ones is still a matter of debate citation needed Unlike rodents which have ever growing teeth multituberculates underwent dental replacement patterns typical to most mammals though in at least some species the lower incisors continued to erupt long after the root s closure 7 Multituberculates are notable for the presence of a massive fourth lower premolar the plagiaulacoid other mammals like Plesiadapiformes and diprotodontian marsupials also have similar premolars in both upper and lower jaws but in multituberculates this tooth is massive and the upper premolars are not modified this way In basal multituberculates all three lower premolars were plagiaulacoids increasing in size posteriorly but in Cimolodonta only the fourth lower premolar remained with the third one remaining only as a vestigial peg like tooth 7 and in several taxa like taeniolabidoideans the plagiaulacoid disappeared entirely or was reconverted into a molariform tooth 8 9 10 nbsp Skull of Ptilodus Notice the massive blade like lower premolar Unlike rodents and similar therians multituberculates had a palinal jaw stroke front to back instead of a propalinal back to front or transverse side to side one as a consequence their jaw musculature and cusp orientation is radically different 4 7 Palinal jaw strokes are almost entirely absent in modern mammals with the possible exception of the dugong 11 but are also present in haramiyidans argyrolagoideans and tritylodontids the former historically united with multituberculates on that basis Multituberculate mastication is thought to have operated in a two stroke cycle first food held in place by the last upper premolar was sliced by the bladelike lower pre molars as the dentary moved orthally upward Then the lower jaw moved palinally grinding the food between the molar cusp rows 4 7 nbsp Lower jaws and teeth of allodontid multituberculatesThe structure of the pelvis in the Multituberculata suggests that they gave birth to tiny helpless underdeveloped young similar to modern marsupials such as kangaroos 2 7 However a 2022 study reveals that they might actually have had long gestation periods like placentals 12 At least two lineages developed hypsodonty in which tooth enamel extends beyond the gumline lambdopsalid taeniolabidoideans 13 and sudamericid gondwanatheres 14 Studies published in 2018 demonstrated that multituberculates had relatively complex brains some braincase regions even absent in therian mammals 15 Evolution editMultituberculates first appear in the fossil record during the Jurassic period and then survived and even dominated for over one hundred million years longer than any other order of mammaliforms including placental mammals The earliest known multituberculates are from the Middle Jurassic Bathonian 166 168 million years ago of England and Russia including Hahnotherium and Kermackodon from the Forest Marble Formation of England and Tashtykia and Tagaria from the Itat Formation of Russia These forms are only known from isolated teeth which bear close similarity to those of euharamyidans which they are suspected to be closely related 16 During the Late Jurassic and Early Cretaceous primitive multituberculates collectively grouped into the paraphyletic Plagiaulacida were abundant and widespread across Laurasia including Europe Asia and North America During the Aptian stage of the Early Cretaceous the advanced subgroup Cimolodonta appeared in North America characterised by a reduced number of lower premolars with a blade like lower fourth premolar By the early Late Cretaceous Cenomanian Cimolodonta had replaced all other multituberculate lineages 17 During the Late Cretaceous multituberculates experienced an adaptive radiation corresponding with a shift towards herbivory 18 Multituberculates reached their peak diversity during the early Paleocene shortly after the Cretaceous Paleogene extinction event but declined from the mid Paleocene onwards likely due to competition with placental mammals such as rodents and ungulates the group finally became extinct in the Late Eocene 19 20 There are some isolated records of multituberculates from the Southern Hemisphere including the cimolodontan Corriebaatar from the Early Cretaceous of Australia 21 and fragmentary remains from the Late Cretaceous Maevarano Formation of Madagascar 22 The family Ferugliotheriidae from the Late Cretaceous of South America traditionally considered gondwanatherians may actually be cimolodontan multituberculates 21 During the Late Cretaceous and Paleocene the multituberculates radiated into a wide variety of morphotypes including the squirrel like arboreal ptilodonts The peculiar shape of their last lower premolar is their most outstanding feature These teeth were larger and more elongated than the other cheek teeth and had an occlusive surface forming a serrated slicing blade Though it can be assumed that this was used for crushing seeds and nuts it is believed that most small multituberculates also supplemented their diet with insects worms and fruits 4 Tooth marks attributed to multituberculates are known on Champsosaurus fossils indicating that at least some of these mammals were scavengers 23 A ptilodont that thrived in North America was Ptilodus Thanks to the well preserved Ptilodus specimens found in the Bighorn Basin Wyoming we know that these multituberculates were able to abduct and adduct their big toes and thus that their foot mobility was similar to that of modern squirrels which descend trees head first 4 nbsp Restoration of CatopsbaatarAnother group of multituberculates the taeniolabids were heavier and more massively built indicating that they lived a fully terrestrial life The largest specimens weighed probably as much as 22 kg 49 lb making them comparable in size to large rodents like the modern beaver 24 25 Classification editMultituberculate is generally placed in the Allotheria alongside Euharamiyida a clade of mammals known from the Middle Jurassic to Early Cretaceous of the Asia and possibly Europe that several morphological similarities to multituberculates 16 26 Gondwanatheria is a monophyletic group of allotherians that was diverse in the Late Cretaceous of South America India Madagascar and possibly Africa and occurs onwards into the Paleogene of South America and Antarctica Their placement within Allotheria is highly controversial with some phylogenies recovering the group as deeply nested within multituberculates while others recover them as a distinct branch of allotherians separate from multituberculates 26 nbsp Restoration of Taeniolabis taoensisIn their 2001 study Kielan Jaworowska and Hurum found that most multituberculates could be referred to two suborders Plagiaulacida and Cimolodonta The exception is the genus Arginbaatar which shares characteristics with both groups Plagiaulacida is paraphyletic representing the more primitive evolutionary grade Its members are the more basal Multituberculata Chronologically they ranged from perhaps the Middle Jurassic until the mid Cretaceous This group is further subdivided into three informal groupings the allodontid line the paulchoffatiid line and the plagiaulacid line Cimolodonta is apparently a natural monophyletic suborder This includes the more derived Multituberculata which have been identified from the lower Cretaceous to the Eocene The superfamilies Djadochtatherioidea Taeniolabidoidea Ptilodontoidea are recognized as is the Paracimexomys group Additionally there are the families Cimolomyidae Boffiidae Eucosmodontidae Kogaionidae Microcosmodontidae and the two genera Uzbekbaatar and Viridomys More precise placement of these types awaits further discoveries and analysis 27 better source needed Taxonomy edit Subgroups nbsp Multituberculate phylogenetic tree 28 Main article List of multituberculate species Based on the combined works of Mikko s Phylogeny Archive 29 and Paleofile com citation needed Suborder Plagiaulacida Simpson 1925 Genus Argillomys Cifelli Gordon amp Lipka 2013 Species Argillomys marylandensis Cifelli Gordon amp Lipka 2013 Genus Janumys Eaton amp Cifelli 2001 Species Janumys erebos Eaton amp Cifelli 2001 Super family Allodontoidea Marsh 1889 Genus Glirodon Engelmann amp Callison 2001 Species G grandis Engelmann amp Callison 2001 Family Arginbaataridae Hahn amp Hahn 1983 Genus Arginbaatar Trofimov 1980 Species A dmitrievae Trofimov 1980 Family Zofiabaataridae Bakker 1992 Genus Zofiabaatar Bakker amp Carpenter 1990 Species Z pulcher Bakker amp Carpenter 1990 Family Allodontidae Marsh 1889 Genus Passumys Cifelli Davis amp Sames 2014 Species Passumys angelli Cifelli Davis amp Sames 2014 Genus Ctenacodon Marsh 1879 Species C serratus Marsh 1879 Species C nanus Marsh 1881 Species C laticeps Marsh 1881 Allodon laticeps Marsh 1881 Species C scindens Simpson 1928 Genus Psalodon Simpson 1926 Species P potens Marsh 1887 Ctenacodon potens Marsh 1887 Species P fortis Marsh 1887 Simpson 1929 Allodon fortis Marsh 1887 Species P marshi Simpson 1929 Super family Paulchoffatioidea Hahn 1969 sensu Hahn amp Hahn 2003 Genus Mojo Hahn LePage amp Wouters 1987 Species Mojo usuratus Hahn LePage amp Wouters 1987 Genus Rugosodon Yuan et al 2013 Species Rugosodon eurasiaticus Yuan et al 2013 Family Pinheirodontidae Hahn amp Hahn 1999 Genus Bernardodon Hahn amp Hahn 1999 Species B atlanticus Hahn amp Hahn 1999 Species B sp Hahn amp Hahn 1999 Genus Cantalera Badiola Canudo amp Cuenca Bescos 2008 Species Cantalera abadi Badiola Canudo amp Cuenca Bescos 2008 Genus Ecprepaulax Hahn amp Hahn 1999 Species E anomala Hahn amp Hahn 1999 Genus Gerhardodon Kielan Jaworowska amp Ensom 1992 Species G purbeckensis Kielan Jaworowska amp Ensom 1992 Genus Iberodon Hahn amp Hahn 1999 Species I quadrituberculatus Hahn amp Hahn 1999 Genus Lavocatia Canudo amp Cuenca Bescos 1996 Species L alfambrensis Canudo amp Cuenca Bescos 1996 Genus Pinheirodon Hahn amp Hahn 1999 Species P pygmaeus Hahn amp Hahn 1999 Species P vastus Hahn amp Hahn 1999 Family Paulchoffatiidae Hahn 1969 Genus Galveodon Hahn amp Hahn 1992 Species G nannothus Hahn amp Hahn 1992 Genus Sunnyodon Kielan Jaworowska amp Ensom 1992 Species S notleyi Kielan Jaworowska amp Ensom 1992 subfamily Paulchoffatiinae Hahn 1971 Genus Paulchoffatia Kuhne 1961 Species P delgador Kuhne 1961 Genus Pseudobolodon Hahn 1977 Species P oreas Hahn 1977 Species P krebsi Hahn amp Hahn 1994 Genus Henkelodon Hahn 1987 Species H naias Hahn 1987 Genus Guimarotodon Hahn 1969 Species G leiriensis Hahn 1969 Genus Meketibolodon Hahn 1978 Hahn 1993 Species M robustus Hahn 1978 Hahn 1993 Pseudobolodon robusutus Hahn 1978 Genus Plesiochoffatia Hahn amp Hahn 1999 Parachoffatia Hahn amp Hahn 1998 non Mangold 1970 Species P thoas Hahn amp Hahn 1998 Hahn amp Hahn 1999 Parachoffatia thoa Hahn amp Hahn 1998 Species P peparethos Hahn amp Hahn 1998 Hahn amp Hahn 1999 Parachoffatia peparethos Hahn amp Hahn 1998 Species P staphylos Hahn amp Hahn 1998 Hahn amp Hahn 1999 Parachoffatia staphylos Hahn amp Hahn 1998 Genus Xenachoffatia Hahn amp Hahn 1998 Species X oinopion Hahn amp Hahn 1998 Genus Bathmochoffatia Hahn amp Hahn 1998 Species B hapax Hahn amp Hahn 1998 Genus Kielanodon Hahn 1987 Species K hopsoni Hahn 1987 Genus Meketichoffatia Hahn 1993 Species M krausei Hahn 1993 Genus Renatodon Hahn 2001 Species Renatodon amalthea Hahn 2001 Subfamily Kuehneodontinae Hahn 1971 Genus Kuehneodon Hahn 1969 Species K dietrichi Hahn 1969 Species K barcasensis Hahn amp Hahn 2001 Species K dryas Hahn 1977 Species K guimarotensis Hahn 1969 Species K hahni Antunes 1988 Species K simpsoni Hahn 1969 Species K uniradiculatus Hahn 1978PlagiaulacoideaSuper family Plagiaulacoidea Ameghino 1894 Family Plagiaulacidae Gill 1872 sensu Kielan Jaworowska amp Hurum 2001 Bolodontidae Osborn 1887 Genus Morrisonodon Hahn amp Hahn 2004 Species Morrisonodon brentbaatar Bakker 1998 Hahn amp Hahn 2004 Ctenacodon brentbaatar Bakker 1998 Genus Plagiaulax Falconer 1857 Species P becklesii Falconer 1857 Species P dawsoni Woodward 1891 Plioprion dawsoni Woodward 1891 Loxaulax dawsoni Woodward 1891 Sloan 1979 Genus Bolodon Owen 1871 Plioprion Cope 1884 Species B crassidens Owen 1871 Species B falconeri Owen 1871 Pligiaulax falconeri Owen 1871 Plioprion falconeri Owen 1871 Species B hydei Cifelli Davis amp Sames 2014 Species B minor Falconer 1857 Pligiaulax minor Falconer 1857 Plioprion minor Falconer 1857 Species B osborni Simpson 1928 Plioprion osborni Simpson 1928 Ctenacodon osborni Simpson 1928 Species B elongatus Simpson 1928 Family Eobaataridae Kielan Jaworowska Dashzeveg amp Trofimov 1987 Genus Eobaatar Kielan Jaworowska Dashzeveg amp Trofimov 1987 Species E clemensi Sweetman 2009 Species E hispanicus Hahn amp Hahn 1992 Species E magnus Kielan Jaworowska Dashzeveg amp Trofimov 1987 Species E minor Kielan Jaworowska Dashzeveg amp Trofimov 1987 Species E pajaronensis Hahn amp Hahn 2001 Genus Hakusanobaatar Kusuhashi et al 2008 Species H matsuoi Kusuhashi et al 2008 Genus Heishanobaatar Kusuhashi et al 2010 Species H triangulus Kusuhashi et al 2010 Genus Iberica Badiola et al 2011 Species Iberica hahni Badiola et al 2011 Genus Liaobaatar Kusuhashi et al 2009 Species L changi Kusuhashi et al 2009 Genus Loxaulax Simpson 1928 Parendotherium Crusafont Pairo amp Adrover 1966 Species L valdensis Woodward 1911 Simpson 1928 Dipriodon valdensis Woodward 1911 Species L herreroi Crusafont Pairo amp Adrover 1966 Parendotherium herreroi Crusafont Pairo amp Adrover 1966 Genus Monobaatar Kielan Jaworowska Dashzeveg amp Trofimov 1987 Species M mimicus Kielan Jaworowska Dashzeveg amp Trofimov 1987 Genus Sinobaatar Hu amp Wang 2002 Species S lingyuanensis Hu amp Wang 2002 Species S xiei Kusuhashi et al 2009 Species S fuxinensis Kusuhashi et al 2009 Genus Tedoribaatar Kusuhashi et al 2008 Species T reini Kusuhashi et al 2008 Genus Teutonodon Martin et al 2016 Species Teutonodon langenbergensis Martin et al 2016 Family Albionbaataridae Kielan Jaworowska amp Ensom 1994 Genus Albionbaatar Kielan Jaworowska amp Ensom 1994 Species A denisae Kielan Jaworowska amp Ensom 1994 Genus Kielanobaatar Kusuhashi et al 2010 Species K badaohaoensis Kusuhashi et al 2010 Genus Proalbionbaatar Hahn amp Hahn 1998 Species P plagiocyrtus Hahn amp Hahn 1998 Suborder Gondwanatheria McKenna 1971 Gondwanatheroidea Krause amp Bonaparte 1993 Family Groeberiidae Patterson 1952 Genus Groeberia Patterson 1952 Species G minoprioi Ryan Patterson 1952 Species G pattersoni G G Simpson 1970 Genus Klohnia Flynn amp Wyss 1999 Species K charrieri Flynn amp Wyss 1999 Species K major Goin et al 2010 Genus Epiklohnia Goin et al 2010 Species Epiklohnia verticalis Goin et al 2010 Genus Praedens Goin et al 2010 Species Praedens aberrans Goin et al 2010 Family Ferugliotheriidae Bonaparte 1986 Genus Ferugliotherium Bonaparte 1986a Vucetichia Bonaparte 1990 Ferugliotherium windhauseni Bonaparte 1986a Vucetichia gracilis Bonaparte 1990 Genus Trapalcotherium Rougier et al 2008 Trapalcotherium matuastensis Rougier et al 2008 Family Sudamericidae Scillato Yane amp Pascual 1984 Gondwanatheridae Bonaparte 1986 Patagonidae Pascual amp Carlini 1987 Genus Greniodon Goin et al 2012 Greniodon sylvanicus Goin et al 2012 Genus Vintana Krause et al 2014 Vintana sertichi Krause et al 2014 Genus Dakshina Wilson Das Sarama amp Anantharaman 2007 Dakshina jederi Wilson Das Sarama amp Anantharaman 2007 Genus Gondwanatherium Bonaparte 1986 Gondwanatherium patagonicum Bonaparte 1986 Genus Sudamerica Scillato Yane amp Pascual 1984 Sudamerica ameghinoi Scillato Yane amp Pascual 1984 Genus Lavanify Krause et al 1997 Lavanify miolaka Krause et al 1997 Genus Bharattherium Prasad et al 2007 Bharattherium bonapartei Prasad et al 2007 Genus Patagonia Pascual amp Carlini 1987 Patagonia peregrina Pascual amp Carlini 1987 CimolodontaSuborder Cimolodonta McKenna 1975 Genus Allocodon non Marsh 1881 Species A fortis Marsh 1889 Species A lentus Marsh 1892 Cimolomys lentus Species A pumilis Marsh 1892 Cimolomys pumilus Species A rarus Marsh 1889 Genus Ameribaatar Eaton amp Cifelli 2001 Species A zofiae Eaton amp Cifelli 2001 Genus Bubodens Wilson 1987 Species Bubodens magnus Wilson 1987 Genus Clemensodon Krause 1992 Species Clemensodon megaloba Krause 1992 Kimbetohia cambi in partim Genus Fractinus Higgins 2003 Species Fractinus palmorum Higgins 2003 Genus Uzbekbaatar Kielan Jaworowska amp Nesov 1992 Species Uzbekbaatar kizylkumensis Kielan Jaworowska amp Nesov 1992 Genus Viridomys Fox 1971 Species Viridomys orbatus Fox 1971 Family Corriebaataridae Rich et al 2009 Genus Corriebaatar Rich et al 2009 Species Corriebaatar marywaltersae Rich et al 2009 Paracimexomys group Genus Paracimexomys Archibald 1982 Species P crossi Cifelli 1997 Species P dacicus Grigorescu amp Hahn 1989 Species P oardaensis Codrea et al 2014 Barbatodon oardaensis Codrea et al 2014 Species P magnus Sahni 1972 Archibald 1982 Cimexomys magnus Sahni 1972 Species P magister Fox 1971 Archibald 1982 Cimexomys magister Fox 1971 Species P perplexus Eaton amp Cifelli 2001 Species P robisoni Eaton amp Nelson 1991 Species P priscus Lillegraven 1969 Archibald 1982 Cimexomys priscus Lillegraven 1969 genotype Paracimexomys sensu Eaton amp Cifelli 2001 Species P propriscus Hunter Heinrich amp Weishampel 2010 Genus Cimexomys Sloan amp Van Valen 1965 Species C antiquus Fox 1971 Species C gregoryi Eaton 1993 Species C judithae Sahni 1972 Paracimexomys judithae Sahni 1972 Archibald 1982 Species C arapahoensis Middleton amp Dewar 2004 Species C minor Sloan amp Van Valen 1965 Species C gratus Jepson 1930 Lofgren 1995 Cimexomys hausoi Archibald 1983 Eucosmodon gratus Jepson 1930 Mesodma ambigua Jepson 1940 Stygimus gratus Jepson 1930 Genus Bryceomys Eaton 1995 Species B fumosus Eaton 1995 Species B hadrosus Eaton 1995 Species B intermedius Eaton amp Cifelli 2001 Genus Cedaromys Eaton amp Cifelli 2001 Species C bestia Eaton amp Nelson 1991 Eaton amp Cifelli 2001 Paracimexomys bestia Eaton amp Nelson 1991 Species C hutchisoni Eaton 2002 Species C minimus Eaton 2009 Species C parvus Eaton amp Cifelli 2001 Genus Dakotamys Eaton 1995 Species D sp Eaton 1995 Species D malcolmi Eaton 1995 Species D shakespeari Eaton 2013 Family Boffidae Hahn amp Hahn 1983 sensu Kielan Jaworowska amp Hurum 2001 Genus Boffius Vianey Liaud 1979 Species Boffius splendidus Vianey Liaud 1979 Boffiidae Hahn amp Hahn 1983 sensu Kielan Jaworowska amp Hurum 2001 Family Cimolomyidae Marsh 1889 sensu Kielan Jaworowska amp Hurum 2001 Genus Paressodon Wilson Dechense amp Anderson 2010 Species Paressodon nelsoni Wilson Dechense amp Anderson 2010 Genus Cimolomys Marsh 1889 Allacodon Marsh 1889 Selenacodon Marsh 1889 Species C clarki Sahni 1972 Species C gracilis Marsh 1889 Cimolomys digona Marsh 1889 Meniscoessus brevis Ptilodus gracilis Osborn 1893 non Gidley 1909 Selenacodon brevis Marsh 1889 Species C trochuus Lillegraven 1969 Species C milliensis Eaton 1993a Species C bellus Marsh 1889 Genus Essonodon Simpson 1927 Species E browni Simpson 1927 cimolodontidae Kielan Jaworowska amp Hurum 2001 Genus Buginbaatar Kielan Jaworowska amp Sochava 1969 Species Buginbaatar transaltaiensis Kielan Jaworowska amp Sochava 1969 Genus Meniscoessus Cope 1882 Dipriodon Marsh 1889 Tripriodon Marsh 1889 nomen dubium Triprotodon Chure amp McIntosh 1989 nomen dubium Selenacodon Marsh 1889 Halodon Marsh 1889 Oracodon Marsh 1889 Species M caperatus Marsh 1889 Species M collomensis Lillegraven 1987 Species M conquistus Cope 1882 Species M ferox Fox 1971a Species M intermedius Fox 1976b Species M major Russell 1936 Cimolomys major Russell 1937 Species M robustus Marsh 1889 Dipriodon robustus Marsh 1889 Dipriodon lacunatus Marsh 1889 Tripriodon coelatus Marsh 1889 Meniscoessus coelatus Marsh 1889 Selenacodon fragilis Marsh 1889 Meniscoessus fragilis Marsh 1889 Halodon sculptus Marsh 1889 Cimolomys sculptus Marsh 1889 Meniscoessus sculptus Marsh 1889 Oracodon anceps Marsh 1889 Oracodon conulus Marsh 1892 Meniscoessus borealis Simpson 1927c Meniscoessus greeni Wilson 1987 Species M seminoensis Eberle amp Lillegraven 1998a Family Kogaionidae Radulescu amp Samson 1996 Genus Kogaionon Radulescu amp Samson 1996 Species K ungureanui Radulescu amp Samson 1996 Genus Hainina Vianey Liaud 1979 Species H belgica Vianey Liaud 1979 Species H godfriauxi Vianey Liaud 1979 Species H pyrenaica Pelaez Campomanes Lopez Martinez Alvarez Sierra amp Daams 2000 Species H vianeyae Pelaez Campomanes Lopez Martinez Alvarez Sierra amp Daams 2000 Genus Barbatodon Radulescu amp Samson 1986 Species B transylvanicum Radulescu amp Samson 1986 Family Eucosmodontidae Jepsen 1940 sensu Kielan Jaworowska amp Hurum 2001 Eucosmodontidae Eucosmodontinae Jepsen 1940 sensu McKenna amp Bell 1997 Genus Eucosmodon Matthew amp Granger 1921 Species E primus Granger amp Simpson 1929 Species E americanus Cope 1885 Species E molestus Cope 1869 Neoplagiaulax molestus Cope 1869 Genus Stygimys Sloan amp Van Valen 1965 Species S camptorhiza Johnston amp Fox 1984 Species S cupressus Fox 1981 Species S kuszmauli Eucosmodon kuszmauli Species S jepseni Simpson 1935 Species S teilhardi Granger amp Simpson 1929 Family Microcosmodontidae Holtzman amp Wolberg 1977 Eucosmodontidae Microcosmodontinae Holtzman amp Wolberg 1977 sensu McKenna amp Bell 1997 Genus PentacosmodonJepsen 1940 Species P pronus Jepsen 1940 Djadochtatheroid Kielan Jaworowska amp Hurum 2001 Genus Acheronodon Archibald 1982 Species A garbani Archibald 1982 Genus Microcosmodon Jepsen 1930 Species M conus Jepsen 1930 Species M rosei Krause 1980 Species M arcuatus Johnston amp Fox 1984 Species M woodi Holtzman amp Wolberg 1977 Eucosmodontine Species M harleyi Weil 1998 Superfamily Ptilodontoidea Cope 1887 sensu McKenna amp Bell 1997 e Kielan Jaworowska amp Hurum 2001 Family Cimolodontidae Marsh 1889 sensu Kielan Jaworowska amp Hurum 2001 Genus Liotomus Lemoine 1882 Neoctenacodon Lemoine 1891 Species L marshi Lemoine 1882 Cope 1884 Neoctenacodon marshi Lemoine 1882 Neoplagiaulax marshi Lemoine 1882 Plagiaulax marshi Lemoine 1882 Eucosmodontidae McKenna amp Bell 1997 Genus Yubaatar Xu et al 2015 Species Yubaatar zhongyuanensis Xu et al 2015 Genus Anconodon Jepsen 1940 Species A lewisi Simpson 1935 Sloan 1987 Species A gibleyi Simpson 1935 Ptilodus gidleyi Simpson 1935 Species A cochranensis Russell 1929 Liotomus russelli Simpson 1935 Anconodon russelli Simpson 1935 Sloan 1987 Ectopodon cochranensis Russell 1967 Genus Cimolodon Marsh 1889 Nanomys Marsh 1889 Nanomyops Marsh 1892 Species C agilis Marsh 1889 Species C foxi Eaton 2002 Species C gracilis Marsh 1889 Species C electus Fox 1971 Species C nitidus Marsh 1889 Allacodon rarus Marsh 1892 sensu Clemens 1964a Nanomys minutus Marsh 1889 Nanomyops minutus Marsh 1889 Marsh 1892 Halodon serratus Marsh 1889 Ptilodus serratus Marsh 1889 Gidley 1909 Species C parvus Marsh 1889 Species C peregrinus Donohue Wilson amp Breithaupt 2013 Species C similis Fox 1971 Species C wardi Eaton 2006 Family Incertae sedis Genus Neoliotomus Jepsen 1930 Species N conventus Jepsen 1930 Species N ultimus Granger amp Simpson 1928 Family Neoplagiaulacidae Ameghino 1890 Ptilodontidae Neoplagiaulacinae Ameghino 1890 sensu McKenna amp Bell 1997 Genus Mesodma Jepsen 1940 Species M hensleighi Lillegraven 1969 Species M senecta Fox 1971 Species M ambigua Jepsen 1940 Species M pygmaea Sloan 1987 Species M formosa Marsh 1889 Halodon formosus Marsh 1889 Species M primaeva Lambe 1902 Species M thompsoni Clemens 1964 Genus Ectypodus Matthew amp Cranger 1921 Charlesmooria Kuhne 1969 Species E aphronorus Sloan 1981 Species E childei Kuhne 1969 Species E elaphus Scott 2005 Species E lovei Sloan 1966 Krishtlaka amp Black 1975 Species E musculus Matthew amp Granger 1921 Species E powelli Jepsen 1940 Species E simpsoni Jepsen 1930 Species E szalayi Sloan 1981 Species E tardus Jepsen 1930 Genus Mimetodon Jepsen 1940 Species M krausei Sloan 1981 Species M nanophus Holtzman 1978 Neoplagiaulax nanophus Holtzman 1978 Species M siberlingi Simpson 1935 Schiebout 1974 Species M churchilli Jepsen 1940 Genus Neoplagiaulax Lemoine 1882 Species N annae Vianey Liaud 1986 Species N burgessi Archibald 1982 Species N cimolodontoides Scott 2005 Species N copei Lemoine 1885 Species N donaldorum Scott amp Krause 2006 Species N eocaenus Lemoine 1880 Species N grangeri Simpson 1935 Species N hazeni Jepsen 1940 Species N hunteri Krishtalka 1973 Species N jepi Sloan 1987 Species N kremnus Johnston amp Fox 1984 Species N macintyrei Slaon 1981 Species N macrotomeus Wilson 1956 Species N mckennai Sloan 1987 Species N nelsoni Sloan 1987 Species N nicolai Vianey Liaud 1986 Species N paskapooensis Scott 2005 Species N serrator Scott 2005 Species N sylvani Vianey Liaud 1986 Genus Parectypodus Jepsen 1930 Species P armstrongi Johnston amp Fox 1984 Species P corystes Scott 2003 Species P foxi Storer 1991 Species P laytoni Jepsen 1940 Species P lunatus Krause 1982 P childei Kuhne 1969 Species P simpsoni Jepsen 1940 Species P sinclairi Simpson 1935 Species P sloani Schiebout 1974 Species P trovessartianus Cope 1882 P trouessarti Ptilodus Mimetodon Neoplagiaulax Species P sylviae Rigsby 1980 Ectypodus sylviae Rigby 1980 Species P vanvaleni Sloan 1981 Genus Cernaysia Vianey Liaud 1986 Species C manueli Vianey Liaud 1986 Species C davidi Vianey Liaud 1986 Genus Krauseia Vianey Liaud 1986 Species K clemensi Sloan 1981 Parectypodus clemensi Sloan 1981 Genus XyronomysRigby 1980 Species X swainae Rigby 1980 Xironomys sic Eucosmodontidae Genus Xanclomys Rigby 1980 Species X mcgrewiRigby 1980 Genus Mesodmops Tong amp Wang 1994 Species M dawsonae Tong amp Wang 1994 Family Ptilodontidae Cope 1887 Ptilodontidae Ptilodontinae Cope 1887 sensu McKenna amp Bell 1997 Genus Kimbetohia Simpson 1936 Species K cambi Granger Gregory amp Colbert in Matthew 1937 or Simpson 1936 Species K sp cf K cambi Genus Ptilodus Cope 1881 Chirox Cope 1884 Species P fractus Species P kummae Krause 1977 Species P gnomus Scott Fox amp Youzwyshyn 2002 cf Ectypodus hazeni Jepsen 1940 Gazin 1956 Species P mediaevus Cope 1881 Ptilodus plicatus Cope 1884 Chirox plicatus Cope 1884 P ferronensis Gazin 1941 Species P montanus Douglass 1908 P gracilis Gidley 1909 P admiralis Hay 1930 Species P tsosiensis Sloan 1981 Species P wyomingensis Jepsen 1940 Genus Baiotomeus Krause 1987 Species B douglassi Simpson 1935 Ptilodus Mimetodon Neoplagiaulax Species B lamberti Krause 1987 Species B russelli Scott Fox amp Youzwyshyn 2002 Species B rhothonion Scott 2003 Genus Prochetodon Jepsen 1940 Species P cavus Jespen 1940 Species P foxi Krause 1987 Species P taxus Krause 1987 Species P speirsae Scott 2004 Superfamily Taeniolabidoidea Granger amp Simpson 1929 sensu Kielan Jaworowska amp Hurum 2001 Genus Prionessus Matthew amp Granger 1925 Species P lucifer Matthew amp Granger 1925 Family Lambdopsalidae Genus Lambdopsalis Chow amp Qi 1978 Species L bulla Chow amp Qi 1978 Genus Sphenopsalis Matthew Granger amp Simpson 1928 Species S nobilis Matthew Granger amp Simpson 1928 Family Taeniolabididae Granger amp Simpson 1929 Genus Taeniolabis Cope 1882 Species T lamberti Simmons 1987 Species T taoensis Cope 1882 Genus Kimbetopsalis Species K simmonsae Superfamily Djadochtatherioidea Kielan Jaworowska amp Hurum 1997 sensu Kielan Jaworowska amp Hurum 2001 Djadochtatheria Kielan Jaworowska amp Hurum 1997 Genus Bulganbaatar Kielan Jaworowska 1974 Species B nemegtbaataroides Kielan Jaworowska 1974 Genus Nemegtbaatar Kielan Jaworowska 1974 Species N gobiensis Kielan Jaworowska 1974 Family Chulsanbaataridae Kielan Jaworowska 1974 Genus Chulsanbaatar Kielan Jaworowska 1974 Species C vulgaris Kielan Jaworowska 1974 Family Sloanbaataridae Kielan Jaworowska 1974 Genus Kamptobaatar Kielan Jaworowska 1970 Species K kuczynskii Kielan Jaworowska 1970 Genus Nessovbaatar Kielan Jaworowska amp Hurum 1997 Species N multicostatus Kielan Jaworowska amp Hurum 1997 Genus Sloanbaatar Kielan Jaworowska 1974 Species S mirabilis Kielan Jaworowska 1974 Sloanbaatarinae Family Djadochtatheriidae Kielan Jaworowska Hurum 1997 Genus Djadochtatherium Simpson 1925 Species D matthewi Simpson 1925 Catopsalis matthewi Simpson 1925 Genus Catopsbaatar Kielan Jaworowska 1974 Species C catopsaloides Kielan Jaworowska 1974 Kielan Jaworowska 1994 Djadochtatherium catopsaloides Kielan Jaworowska 1974 Genus Tombaatar Kielan Jaworowska 1974 Species T sabuli Rougier Novacek amp Dashzeveg 1997 Genus Kryptobaatar Kielan Jaworowska 1970 Gobibaatar Kielan Jaworowska 1970 Tugrigbaatar Kielan Jaworowska amp Dashzeveg 1978 Species K saichanensis Kielan Jaworowska amp Dashzeveg 1978 Tugrigbaatar saichaenensis Kielan Jaworowska amp Dashzeveg 1978 Species K dashzevegi Kielan Jaworowska 1970 Species K mandahuensis Smith Guo amp Sun 2001 Species K gobiensis Kielan Jaworowska 1970 Gobibaatar parvus Kielan Jaworowska 1970 Phylogeny 28 edit Multituberculata PaulchoffatiidaePlagiaulacidaeEobaataridaeGondwanatheria FerugliotheriidaeGroeberiidaeSudamericidaeCimolodonta CimolodontidaePtilodontoideaCimexomysCimolomyidaeBoffiusBuginbaatarEucosmodontidaeMicrocosmodontidaeDjadochtatherioidea BulganbaatarChulsanbaatarSloanbaataridaeNemegtbaatarDjadochtatheriidaeKogaionidaeTaeniolabidoidea YubaatarBubodensValenopsalisLambdopsalidaeTaeniolabididaePaleoecology editBehaviour edit Multituberculates are some of the earliest mammals to display complex social behaviours One species Filikomys from the Late Cretaceous of North America engaged in multi generational group nesting and burrowing 30 Extinction edit The extinction of multituberculates has been a topic of controversy for several decades 31 After at least 88 million years of dominance over most mammalian assemblies multituberculates reached the peak of their diversity in the early Palaeocene before gradually declining across the final stages of the epoch and the Eocene finally disappearing in the early Oligocene 32 The last multituberculate species Ectypodus childei went extinct near the end of the Eocene in North America It is unclear why this particular species persisted for so long when all of its counterparts succumbed to replacement by rodents 33 43 Traditionally the extinction of multituberculates has been linked to the rise of rodents and to a lesser degree earlier placental competitors like hyopsodonts and Plesiadapiformes which supposedly competitively excluded multituberculates from most mammalian faunas 1 However the idea that multituberculates were replaced by rodents and other placentals has been criticised by several authors For one thing it relies on the assumption that these mammals are inferior to more derived placentals and ignores the fact that rodents and multituberculates had co existed for at least 15 million years According to some researchers multituberculate decline is shaped by sharp extinction events most notably after the Tiffanian where a sudden drop in diversity occurs Finally the youngest known multituberculates do not exemplify patterns of competitive exclusion the Oligocene Ectypodus is a rather generalistic species rather than a specialist This combination of factors suggests that rather than gradually declining due to pressure from rodents and similar placentals multituberculates simply could not cope with climatic and vegetation changes as well as the rise of new predatory eutherians such as miacids 32 More recent studies show a mixed effect Multituberculate faunas in North America and Europe do indeed decline in correlation to the introduction of rodents in these areas However Asian multituberculate faunas co existed with rodents with minimal extinction events implying that competition was not the main cause for the extinction of Asiatic multituberculates As a whole it seems that Asian multituberculates unlike North American and European species never recovered from the KT event which allowed the evolution and propagation of rodents in the first place 31 A recent study seems to indeed indicate that eutherians recovered more quickly from the KT event than multituberculates 34 Conversely another study has shown that placental radiation did not start significantly until after the decline of multituberculates 20 References edit a b Krause David W 1986 Competitive exclusion and taxonomic displacement in the fossil record Vertebrates Phylogeny and Philosophy pp 95 117 doi 10 2113 gsrocky 24 special paper 3 95 ISBN 978 0 941570 02 2 a b Weil Anne June 1997 Introduction to Multituberculates The Lost Tribe of Mammals Berkeley UCMP Chen Meng Philip Wilson Gregory 2015 A multivariate approach to infer locomotor modes in Mesozoic mammals Paleobiology 41 2 280 312 Bibcode 2015Pbio 41 280C doi 10 1017 pab 2014 14 S2CID 86087687 a b c d e Agusti Anton 2002 pp 3 4 Benton Michael J Vertebrate Palaeontology 2004 p 300 Carrano Matthew T and Richard W Blob Timothy J Gaudin and John R Wible 2006 Amniote Paleobiology Perspectives on the Evolution of Mammals Birds and Reptiles p 358 a b c d e Kielan Jaworowska Zofia Richard L Cifelli and Zhe Xi Luo 2005 Mammals from the Age of Dinosaurs Origins Evolution and Structure p 299 Gurovich 2005 p 334 full citation needed Gurovich Yamila Beck Robin March 2009 The Phylogenetic Affinities of the Enigmatic Mammalian Clade Gondwanatheria Journal of Mammalian Evolution 16 1 25 49 doi 10 1007 s10914 008 9097 3 S2CID 42799370 Rougier et al 2009 p 233 full citation needed Lanyon J M Sanson G D February 2006 Degenerate dentition of the dugong Dugong dugon or why a grazer does not need teeth morphology occlusion and wear of mouthparts Journal of Zoology 268 2 133 152 doi 10 1111 j 1469 7998 2005 00004 x New study challenges old views on what s primitive in mammalian reproduction 25 July 2022 Williamson Thomas E Brusatte Stephen L Secord Ross Shelley Sarah 2015 A new taeniolabidoid multituberculate Mammalia from the middle Puercan of the Nacimiento Formation New Mexico and a revision of taeniolabidoid systematics and phylogeny Zoological Journal of the Linnean Society 177 183 208 doi 10 1111 zoj 12336 Gondwanatheria dead link Crompton A W Musinsky C Rougier G W Bhullar B A S Miyamae J A September 2018 Origin of the Lateral Wall of the Mammalian Skull Fossils Monotremes and Therians Revisited Journal of Mammalian Evolution 25 3 301 313 doi 10 1007 s10914 017 9388 7 S2CID 16072755 a b Averianov Alexander O Martin Thomas Lopatin Alexey V Schultz Julia A Schellhorn Rico Krasnolutskii Sergei Skutschas Pavel Ivantsov Stepan May 2021 Multituberculate mammals from the Middle Jurassic of Western Siberia Russia and the origin of Multituberculata Papers in Palaeontology 7 2 769 787 doi 10 1002 spp2 1317 ISSN 2056 2799 S2CID 219067218 Weaver Lucas N Wilson Gregory P Krumenacker L J Mclaughlin Kayla Moore Jason R Varricchio David J 2019 03 04 New multituberculate mammals from the mid Cretaceous lower Cenomanian Wayan Formation of southeastern Idaho and implications for the early evolution of Cimolodonta Journal of Vertebrate Paleontology 39 2 e1604532 Bibcode 2019JVPal 39E4532W doi 10 1080 02724634 2019 1604532 ISSN 0272 4634 S2CID 196655261 Wilson Gregory P Evans Alistair R Corfe Ian J Smits Peter D Fortelius Mikael Jernvall Jukka March 2012 Adaptive radiation of multituberculate mammals before the extinction of dinosaurs Nature 483 7390 457 460 Bibcode 2012Natur 483 457W doi 10 1038 nature10880 ISSN 1476 4687 PMID 22419156 S2CID 4419772 Adams Neil F Rayfield Emily J Cox Philip G Cobb Samuel N Corfe Ian J March 2019 Functional tests of the competitive exclusion hypothesis for multituberculate extinction Royal Society Open Science 6 3 181536 Bibcode 2019RSOS 681536A doi 10 1098 rsos 181536 ISSN 2054 5703 PMC 6458384 PMID 31032010 a b Brocklehurst Neil Panciroli Elsa Benevento Gemma Louise Benson Roger B J July 2021 Mammaliaform extinctions as a driver of the morphological radiation of Cenozoic mammals Current Biology 31 13 2955 2963 e4 doi 10 1016 j cub 2021 04 044 PMID 34004143 S2CID 234782605 a b Rich Thomas Trusler Peter Kool Lesley White Matt A Bevitt Joseph Morton Steven Vickers Rich Patricia 2022 Second specimen of Corriebaatar marywaltersae from the Lower Cretaceous of Australia confirms its multituberculate affinities Acta Palaeontologica Polonica 67 doi 10 4202 app 00924 2021 ISSN 0567 7920 S2CID 247905998 Krause David W Hoffmann Simone Werning Sarah December 2017 First postcranial remains of Multituberculata Allotheria Mammalia from Gondwana Cretaceous Research 80 91 100 Bibcode 2017CrRes 80 91K doi 10 1016 j cretres 2017 08 009 Longrich Nicholas R Ryan Michael J 2010 Mammalian tooth marks on the bones of dinosaurs and other Late Cretaceous vertebrates Palaeontology 53 4 703 709 Bibcode 2010Palgy 53 703L doi 10 1111 j 1475 4983 2010 00957 x Krause et al 2021 Wilson et al 2012 a b Hoffmann Simone Beck Robin M D Wible John R Rougier Guillermo W Krause David W 2020 12 14 Phylogenetic placement of Adalatherium hui Mammalia Gondwanatheria from the Late Cretaceous of Madagascar implications for allotherian relationships Journal of Vertebrate Paleontology 40 sup1 213 234 Bibcode 2020JVPal 40S 213H doi 10 1080 02724634 2020 1801706 ISSN 0272 4634 S2CID 230968231 Dykes Multituberculata Cope 1884 a b Nicolas R Chimento Federico L Agnolin Fernando E Novas 2015 The bizarre metatherians Groeberia and Patagonia late surviving members of gondwanatherian mammals Historical Biology An International Journal of Paleobiology 27 5 603 623 doi 10 1080 08912963 2014 903945 hdl 11336 85076 S2CID 216591096 Mikko s Phylogeny Archive Haaramo Mikko 2007 Mammaliaformes mammals and near mammals Retrieved 30 December 2015 Weaver Lucas N Varricchio David J Sargis Eric J Chen Meng Freimuth William J Wilson Mantilla Gregory P 2 November 2020 Early mammalian social behaviour revealed by multituberculates from a dinosaur nesting site Nature Ecology amp Evolution 5 1 32 37 doi 10 1038 s41559 020 01325 8 PMID 33139921 S2CID 226241443 a b Wood D Joseph 2010 The Extinction of the Multituberculates Outside North America a Global Approach to Testing the Competition Model M S The Ohio State University Archived from the original on 2015 04 08 Retrieved 2015 04 03 a b Ostrander Gregg 1 January 1984 The Early Oligocene Chadronian Raben Ranch Local Fauna Northwest Nebraska Multituberculata with Comments on the Extinction of the Allotheria Transactions of the Nebraska Academy of Sciences and Affiliated Societies Wood D Joseph 2010 The Extinction of the Multituberculates Outside North America a Global Approach to Testing the Competition Model Thesis The Ohio State University Archived from the original on 2023 05 19 Retrieved 2023 05 19 Pires Mathias M Rankin Brian D Silvestro Daniele Quental Tiago B 1804 Diversification dynamics of mammalian clades during the K Pg mass extinction Biology Letters 14 9 2058 doi 10 1098 rsbl 2018 0458 PMC 6170748 PMID 30258031 Sources edit nbsp Wikimedia Commons has media related to Multituberculata nbsp Wikispecies has information related to Multituberculata Agusti Jordi Anton Mauricio 2002 Mammoths Sabertooths and Hominids 65 Millions Years of Mammalian Evolution in Europe New York Columbia University Press ISBN 978 0 231 11640 4 Dykes Trevor Multituberculata Cope 1884 Archived from the original on December 28 2009 Kielan Jaworowska Zofia Hurum Jorn H 2001 Phylogeny and Systematics of multituberculate mammals PDF Palaeontology 44 3 389 429 Bibcode 2001Palgy 44 389K doi 10 1111 1475 4983 00185 S2CID 83592270 Retrieved from https en wikipedia org w index php title Multituberculata amp oldid 1198886061, wikipedia, wiki, book, books, library,

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