Morganucodon: Difference between revisions
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{{Short description| |
{{Short description|Early mammaliaform genus of the Triassic and Jurassic periods}} |
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{{Automatic taxobox |
{{Automatic taxobox |
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| fossil_range = [[Late Triassic]]-[[Middle Jurassic]] {{Fossilrange|Rhaetian|Bathonian}} |
| fossil_range = [[Late Triassic]]-[[Middle Jurassic]] {{Fossilrange|Rhaetian|Bathonian}} |
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| type_species_authority = Kühne, 1949 |
| type_species_authority = Kühne, 1949 |
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| subdivision_ranks = Species |
| subdivision_ranks = Species |
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| subdivision = * {{Extinct}}'''''M. watsoni''''' |
| subdivision = * {{Extinct}}'''''M. watsoni''''' {{small|(Kühne, 1949)}} |
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* {{Extinct}}'''''M. oehleri''''' |
* {{Extinct}}'''''M. oehleri''''' {{small|(Rigney, 1963)}} |
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* {{Extinct}}'''''M. heikuopengensis''''' |
* {{Extinct}}'''''M. heikuopengensis''''' {{small|(Young, 1978)}} |
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* {{Extinct}}'''''M. peyeri''''' |
* {{Extinct}}'''''M. peyeri''''' {{small|(Clemens, 1980)}} |
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* {{Extinct}}'''''M. tardus''''' |
* {{Extinct}}'''''M. tardus''''' {{small|(Butler and Sigogneau-Russell, 2016)}} |
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}} |
}} |
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'''''Morganucodon''''' ("[[Glamorgan]] [[tooth]]") is an early [[mammaliaform]] [[genus]] that lived from the [[Late Triassic]] to the [[Middle Jurassic]]. It first appeared about 205 million years ago. Unlike many other early mammaliaforms, ''Morganucodon'' is well represented by abundant and well preserved (though in the vast majority of cases disarticulated) material. Most of this comes from [[Glamorgan]] in [[Wales]] (''Morganucodon watsoni''), but fossils have also been found in [[Yunnan]] Province in [[China]] (''Morganucodon oehleri'') and various parts of Europe and North America. Some closely related animals (''[[Megazostrodon]]'') are known from exquisite fossils from [[South Africa]].<ref>Pages 21–33, 174 in [[Zofia Kielan-Jaworowska]], Richard L. Cifelli, and Zhe-Xi Luo, ''Mammals from the Age of Dinosaurs: Origins, Evolution, and Structure'', Columbia University Press, New York, 2004 {{ISBN|0-231-11918-6}}</ref> |
'''''Morganucodon''''' ("[[Glamorgan]] [[tooth]]") is an early [[mammaliaform]] [[genus]] that lived from the [[Late Triassic]] to the [[Middle Jurassic]]. It first appeared about 205 million years ago. Unlike many other early mammaliaforms, ''Morganucodon'' is well represented by abundant and well preserved (though in the vast majority of cases disarticulated) material. Most of this comes from [[Glamorgan]] in [[Wales]] (''Morganucodon watsoni''), but fossils have also been found in [[Yunnan]] Province in [[China]] (''Morganucodon oehleri'') and various parts of Europe and North America. Some closely related animals (''[[Megazostrodon]]'') are known from exquisite fossils from [[South Africa]].<ref>Pages 21–33, 174 in [[Zofia Kielan-Jaworowska]], Richard L. Cifelli, and Zhe-Xi Luo, ''Mammals from the Age of Dinosaurs: Origins, Evolution, and Structure'', Columbia University Press, New York, 2004 {{ISBN|0-231-11918-6}}</ref> |
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The name comes from a Latinization of ''Morganuc'', |
The name comes from a Latinization of ''Morganuc'', the name for South [[Glamorgan]] in the [[Domesday Book]], the county of [[Wales]] where it was discovered by [[Walter Georg Kühne]],<ref name=":0">Walter G. Kühne, "On a Triconodont tooth of a new pattern from a Fissure-filling in South Glamorgan", ''Proceedings of the Zoological Society of London'', volume 119 (1949–1950) pages 345–350</ref> giving the meaning "Glamorgan tooth". |
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== History of discovery == |
== History of discovery == |
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[[File:Morganucodon watsoni.JPG|thumb|left|Lower jaw of ''M. watsoni'', Natural History Museum, London]] |
[[File:Morganucodon watsoni.JPG|thumb|left|Lower jaw of ''M. watsoni'', Natural History Museum, London]] |
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In the summer of 1947, fieldwork was done at Duchy Quarry in [[Glamorgan]] in southern Wales. Grey [[Conglomerate (geology)|conglomerate]] that formed fissure fill deposits within [[ |
In the summer of 1947, fieldwork was done at Duchy Quarry in [[Glamorgan]] in southern Wales. Grey [[Conglomerate (geology)|conglomerate]] that formed fissure fill deposits within [[karst]]ic voids in [[Carboniferous Limestone|Carboniferous limestone]] was extracted. In 1949, [[Walter Georg Kühne]] noted the lower cheek tooth of a primitive mammal while examining samples of the rock. He named it ''Morganucodon watsoni,'' with the genus name being derived from Morganuc, which Kühne stated was the name of South [[Glamorgan]] in the [[Domesday Book]], with the species name being in honour of [[D. M. S. Watson]].<ref name=":0" /> Additional remains of ''M. watsoni'' were described by Kühne in 1958.<ref>{{Cite journal|last=Kühne|first=Walter Georg|date=1958-08-01|title=Rhaetische Triconodonten aus Glamorgan, ihre Stellung zwischen den Klassen Reptilia und Mammalia und ihre Bedeutung für die REICHART'sche Theorie|trans-title=Rhaetian triconodonts from Glamorgan, their position between the classes Reptilia and Mammalia and their significance for REICHART's theory.|url=https://doi.org/10.1007/BF02989032|journal=Paläontologische Zeitschrift|language=de|volume=32|issue=3|pages=197–235|doi=10.1007/BF02989032|s2cid=128828761|issn=0031-0220}}</ref> Also in 1958, [[Kenneth Kermack]] and Frances Mussett described additional remains from Pant Quarry, about a mile from Duchy Quarry, that had been collected in 1956.<ref name=":1">{{Cite journal|last=Clemens|first=William A.|date=May 1979|title=A problem in morganucodontid taxonomy (Mammalia)|url=https://academic.oup.com/zoolinnean/article-lookup/doi/10.1111/j.1096-3642.1979.tb01898.x|journal=Zoological Journal of the Linnean Society|language=en|volume=66|issue=1|pages=1–14|doi=10.1111/j.1096-3642.1979.tb01898.x}}</ref> In August 1948, an expedition to [[Lufeng, Yunnan|Lufeng]] in [[Yunnan]], China yielded a 1 in (2.5 cm) long skull. It was shortly sent to Beijing (then Peking) and then eventually sent out of China, and deposited with Kenneth Kermack at [[University College London]] in 1960. The specimen was preliminarily described in 1963 by Harold W. Rigney, who noted the similarity to ''Morganucodon'' from Britain, and considered it cogeneric, naming the new species ''Morganucodon oehleri'' in honor of the reverend Edgar T. Oehler, who had originally collected the specimen.<ref>{{Cite journal|last=Rigney|first=Harold W.|date=March 1963|title=A Specimen of Morganucodon from Yunnan|url=http://www.nature.com/articles/1971122a0|journal=Nature|language=en|volume=197|issue=4872|pages=1122–1123|doi=10.1038/1971122a0|bibcode=1963Natur.197.1122R|s2cid=4204736|issn=0028-0836}}</ref> In 1978 [[Yang Zhongjian|C. C. Young]] described ''[[Eozostrodon]] heikuopengensis'' from the Hei Koa Peng locality near Lufeng, based on an associated skull and dentary, as well as a right maxilla and associated dentary.<ref>C.-C. Young. 1978. New materials of Eozostrodon. ''Vertebrata PalAsiatica'' '''16''':1-3</ref> A revision by [[William A. Clemens Jr.|William A. Clemens]] in 1979 assigned this species to ''Morganucodon,'' based on its close similarity to the two previously named species.''<ref name=":1" />'' In 1980 Clemens named the species ''Morganucodon peyeri'', from isolated teeth found in Late Triassic ([[Rhaetian]]) deposits near [[Hallau]], Switzerland, with the species being named after paleontologist [[Bernhard Peyer]].<ref>W. A. Clemens. 1980. [https://www.zobodat.at/pdf/Zitteliana_5_0051-0092.pdf Rhaeto-Liassic mammals from Switzerland and West Germany]. ''Zitteliana'' '''5''':51-92</ref> In 1981, Kermack, Mussett and Rigney published an extensive monograph on the skull of ''Morganucodon''.<ref>{{Cite journal|last1=Kermack|first1=K. A.|last2=Mussett|first2=Frances|last3=Rigney|first3=H. W.|date=January 1981|title=The skull of Morganucodon|url=https://academic.oup.com/zoolinnean/article-lookup/doi/10.1111/j.1096-3642.1981.tb01127.x|journal=Zoological Journal of the Linnean Society|language=en|volume=71|issue=1|pages=1–158|doi=10.1111/j.1096-3642.1981.tb01127.x}}</ref> In 2016 [[Percy M. Butler|Percy Butler]] and [[Denise Sigogneau-Russell]] named the species ''Morganucodon tardus'' from an upper right molar (M34984) collected from the Watton Cliff locality near [[Eype]] in [[Dorset]], England, dating to the late [[Bathonian]] stage of the [[Middle Jurassic]]. The species being named after the Latin ''tardus'', late, in reference to it being the youngest member of the genus.<ref>Butler, P.M. and Sigogneau-Russell, D. 2016. Diversity of triconodonts in the Middle Jurassic of Great Britain. Palaeontologia Polonica 67, 35–65. LSID urn:lsid:zoobank.org: pub: C4D90BB6-A001-4DDB-890E-2061B4793992</ref> |
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==Biology== |
==Biology== |
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[[File:Morganucodon.jpg|left|thumb|[[Life restoration]] of ''M. oehleri'']] |
[[File:Morganucodon.jpg|left|thumb|[[Life restoration]] of ''M. oehleri'']] |
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[[File:Morganucodon skull.svg|left|thumb|Diagram of the skull of ''Morganucodon'', with bones labelled ]] |
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''Morganucodon'' was a small, [[plantigrade]] animal. The tail was moderately long. According to Kemp (2005), "the skull was 2–3 cm in length and a presacral body length of about 10 cm [4 inches]. In general appearance, it would have looked like a shrew or mouse".<ref>Kemp T.S. 2005. ''The origin and evolution of mammals'', Oxford University Press, page 143. {{ISBN|0-19-850760-7}}.</ref> There is evidence that it had specialized glands used for grooming, which may indicate that, like present day mammals, it had fur.<ref name=Fur>{{cite journal| last1=Ruben|first1= J.A. |last2= Jones| first2= T.D. |year=2000|title= Selective Factors Associated with the Origin of Fur and Feathers |journal=[[Integrative and Comparative Biology|American Zoologist]]|volume= 40|pages= 585–596 | doi = 10.1093/icb/40.4.585| issue=4 |doi-access= free}}</ref> |
''Morganucodon'' was a small, [[plantigrade]] animal. The tail was moderately long. According to Kemp (2005), "the skull was 2–3 cm in length and a presacral body length of about 10 cm [4 inches]. In general appearance, it would have looked like a shrew or mouse".<ref>Kemp T.S. 2005. ''The origin and evolution of mammals'', Oxford University Press, page 143. {{ISBN|0-19-850760-7}}.</ref> There is evidence that it had specialized glands used for grooming, which may indicate that, like present day mammals, it had fur.<ref name=Fur>{{cite journal| last1=Ruben|first1= J.A. |last2= Jones| first2= T.D. |year=2000|title= Selective Factors Associated with the Origin of Fur and Feathers |journal=[[Integrative and Comparative Biology|American Zoologist]]|volume= 40|pages= 585–596 | doi = 10.1093/icb/40.4.585| issue=4 |doi-access= free}}</ref> |
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Like present day mammals of similar size and presumed habit, ''Morganucodon'' was likely nocturnal and spent the day in a burrow. There is no direct fossil evidence, but several lines of evidence point to a [[nocturnal bottleneck]] in the evolution of the mammal class, and almost all modern mammals of similar size to ''Morganucodon'' are still nocturnal.<ref>{{cite journal|last1=Hall|first1=M. I.|last2=Kamilar|first2=J. M.|last3=Kirk|first3=E. C.|title=Eye shape and the nocturnal bottleneck of mammals|journal=Proceedings of the Royal Society B: Biological Sciences|date=24 October 2012|volume=279|issue=1749|pages=4962–4968|doi=10.1098/rspb.2012.2258|pmid=23097513|pmc=3497252}}</ref><ref>{{cite journal|last1=Muchlinski|first1=Magdalena N.|title=A comparative analysis of vibrissa count and infraorbital foramen area in primates and other mammals|journal=Journal of Human Evolution|date=June 2010|volume=58|issue=6|pages=447–473|doi=10.1016/j.jhevol.2010.01.012|pmid=20434193}}</ref> Likewise, burrowing was widespread both in non-mammalian [[cynodont]]s and in primitive mammals.<ref>{{cite journal|last1=Damiani|first1=R.|last2=Modesto|first2=S.|last3=Yates|first3=A.|last4=Neveling|first4=J.|title=Earliest evidence of cynodont burrowing|journal=Proceedings of the Royal Society B: Biological Sciences|date=22 August 2003|volume=270|issue=1525|pages=1747–1751|doi=10.1098/rspb.2003.2427|pmid=12965004|pmc=1691433}}</ref><ref>{{cite journal|last1=KIELAN|first1=ZOFIA|last2=GAMBARYAN|first2=PETR P.|title=Postcranial anatomy and habits of Asian multituberculate mammals|journal=Lethaia|date=December 1994|volume=27|issue=4|pages=300|doi=10.1111/j.1502-3931.1994.tb01578.x}}</ref> The logics of [[phylogenetic bracketing]] would make ''Morganucodon'' nocturnal and burrowing too. Plant material from the conifer ''[[Hirmeriella]]'' was also found in the fissure fills, indicating ''Morganucudon'' lived in, or near, a forested area. |
Like present day mammals of similar size and presumed habit, ''Morganucodon'' was likely nocturnal and spent the day in a burrow. There is no direct fossil evidence, but several lines of evidence point to a [[nocturnal bottleneck]] in the evolution of the mammal class, and almost all modern mammals of similar size to ''Morganucodon'' are still nocturnal.<ref>{{cite journal|last1=Hall|first1=M. I.|last2=Kamilar|first2=J. M.|last3=Kirk|first3=E. C.|title=Eye shape and the nocturnal bottleneck of mammals|journal=Proceedings of the Royal Society B: Biological Sciences|date=24 October 2012|volume=279|issue=1749|pages=4962–4968|doi=10.1098/rspb.2012.2258|pmid=23097513|pmc=3497252}}</ref><ref>{{cite journal|last1=Muchlinski|first1=Magdalena N.|title=A comparative analysis of vibrissa count and infraorbital foramen area in primates and other mammals|journal=Journal of Human Evolution|date=June 2010|volume=58|issue=6|pages=447–473|doi=10.1016/j.jhevol.2010.01.012|pmid=20434193}}</ref> Likewise, burrowing was widespread both in non-mammalian [[cynodont]]s and in primitive mammals.<ref>{{cite journal|last1=Damiani|first1=R.|last2=Modesto|first2=S.|last3=Yates|first3=A.|last4=Neveling|first4=J.|title=Earliest evidence of cynodont burrowing|journal=Proceedings of the Royal Society B: Biological Sciences|date=22 August 2003|volume=270|issue=1525|pages=1747–1751|doi=10.1098/rspb.2003.2427|pmid=12965004|pmc=1691433}}</ref><ref>{{cite journal|last1=KIELAN|first1=ZOFIA|last2=GAMBARYAN|first2=PETR P.|title=Postcranial anatomy and habits of Asian multituberculate mammals|journal=Lethaia|date=December 1994|volume=27|issue=4|pages=300|doi=10.1111/j.1502-3931.1994.tb01578.x|s2cid=85021289 }}</ref> The logics of [[phylogenetic bracketing]] would make ''Morganucodon'' nocturnal and burrowing too. Plant material from the conifer ''[[Hirmeriella]]'' was also found in the fissure fills, indicating ''Morganucudon'' lived in, or near, a forested area. |
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The diet appears to have been insects and other small animals, with a preference for hard prey such as beetles.<ref>{{cite journal |last1=Gill |first1=Pamela G. |last2=Purnell |first2=Mark A. |last3=Crumpton |first3=Nick |author-link4=Kate Robson Brown|last4=Robson-Brown |first4=Kate |last5=Gostling |first5=Neil J. |last6=Stampanoni |first6=M. |last7=Rayfield |first7=Emily J. |date=21 August 2014 |title=Dietary specializations and diversity in feeding ecology of the earliest stem mammals |journal=[[Nature (journal)|Nature]] |volume=512 |issue=7514 |pages=303–305 |doi=10.1038/nature13622 |pmid=25143112 |bibcode=2014Natur.512..303G |hdl=2381/29192 |s2cid=4469841 |hdl-access=free }}</ref> Like most modern mammal insectivores, it grew fairly quickly to adult size.<ref>{{cite journal|last=Chinsamy|first=A.|author2=Hurum, J.H.|title=Bone microstructure and growth patterns of early mammals|journal=Acta Palaeontologica Polonica|year=2006|volume=51|issue=2|pages=325–338|url=http://www.app.pan.pl/archive/published/app51/app51-325.pdf|access-date=30 August 2013}}</ref> Its eggs were probably small and leathery, a condition still found in monotremes.<ref>{{cite journal|last=Parente|first=Raphael Câmara Medeiros|author2=Bergqvist, Lílian Paglarelli |author3=Soares, Marina Bento |author4= Filho, Olimpio Barbosa Moraes |title=The history of vaginal birth|journal=Archives of Gynecology and Obstetrics|year=2011|volume=284|issue=1|pages=1–11|doi=10.1007/s00404-011-1918-6|pmid=21547459|s2cid=22997887}}</ref> |
The diet appears to have been insects and other small animals, with a preference for hard prey such as beetles.<ref>{{cite journal |last1=Gill |first1=Pamela G. |last2=Purnell |first2=Mark A. |last3=Crumpton |first3=Nick |author-link4=Kate Robson Brown|last4=Robson-Brown |first4=Kate |last5=Gostling |first5=Neil J. |last6=Stampanoni |first6=M. |last7=Rayfield |first7=Emily J. |date=21 August 2014 |title=Dietary specializations and diversity in feeding ecology of the earliest stem mammals |journal=[[Nature (journal)|Nature]] |volume=512 |issue=7514 |pages=303–305 |doi=10.1038/nature13622 |pmid=25143112 |bibcode=2014Natur.512..303G |hdl=2381/29192 |s2cid=4469841 |hdl-access=free }}</ref> Like most modern mammal insectivores, it grew fairly quickly to adult size.<ref>{{cite journal|last=Chinsamy|first=A.|author2=Hurum, J.H.|title=Bone microstructure and growth patterns of early mammals|journal=Acta Palaeontologica Polonica|year=2006|volume=51|issue=2|pages=325–338|url=http://www.app.pan.pl/archive/published/app51/app51-325.pdf|access-date=30 August 2013}}</ref> Its eggs were probably small and leathery, a condition still found in monotremes.<ref>{{cite journal|last=Parente|first=Raphael Câmara Medeiros|author2=Bergqvist, Lílian Paglarelli |author3=Soares, Marina Bento |author4= Filho, Olimpio Barbosa Moraes |title=The history of vaginal birth|journal=Archives of Gynecology and Obstetrics|year=2011|volume=284|issue=1|pages=1–11|doi=10.1007/s00404-011-1918-6|pmid=21547459|s2cid=22997887}}</ref> |
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The teeth grew in mammalian fashion, with [[deciduous teeth]] being replaced by permanent teeth that were retained throughout the rest of the animal's life.<ref name=Replace>Alexander F. H. van Nievelt and Kathleen K. Smith, "To replace or not to replace: the significance of reduced functional tooth replacement in marsupial and placental mammals", ''Paleobiology'', Volume 31, Issue 2 (June 2005) pages 324–346</ref> The combination of rapid growth in juveniles and a toothless stage at infancy strongly suggests that ''Morganucodon'' raised its young by [[lactation]]; indeed, it may have been among the first animals to do so.<ref>{{cite book|last1=Kielan-Jaworowska|first1=Zofia|last2=Cifelli|first2=Richard L.|last3=Luo|first3=Zhe-Xi|title=Mammals from the age of dinosaurs : origins, evolution, and structure|date=2004|publisher=Columbia University Press|location=New York|isbn=978-0231119184|pages=148–153}}</ref> The molars in the adult had a series of raised humps and edges that fit into each other, allowing for efficient chewing. However, unlike the situation in most later mammals, the upper and lower molars did not occlude properly when they first met; as they wore against each other, however, their shapes were modified by wear to produce a precise fit.<ref>{{cite journal |first1=A. W. |last1=Crompton|last2=Jenkins|first2=F. Jr.|year=1968 |title=Molar occlusion in late Triassic mammals |journal=Biological Reviews |volume=43 |issue=4|pages=427–458 |doi=10.1111/j.1469-185x.1968.tb00966.x|pmid=4886687|s2cid=1044399}}</ref> |
The teeth grew in mammalian fashion, with [[deciduous teeth]] being replaced by permanent teeth that were retained throughout the rest of the animal's life.<ref name=Replace>Alexander F. H. van Nievelt and Kathleen K. Smith, "To replace or not to replace: the significance of reduced functional tooth replacement in marsupial and placental mammals", ''Paleobiology'', Volume 31, Issue 2 (June 2005) pages 324–346</ref> The combination of rapid growth in juveniles and a toothless stage at infancy strongly suggests that ''Morganucodon'' raised its young by [[lactation]]; indeed, it may have been among the first animals to do so.<ref>{{cite book|last1=Kielan-Jaworowska|first1=Zofia|last2=Cifelli|first2=Richard L.|last3=Luo|first3=Zhe-Xi|title=Mammals from the age of dinosaurs : origins, evolution, and structure|date=2004|publisher=Columbia University Press|location=New York|isbn=978-0231119184|pages=148–153}}</ref> The molars in the adult had a series of raised humps and edges that fit into each other, allowing for efficient chewing. However, unlike the situation in most later mammals, the upper and lower molars did not occlude properly when they first met; as they wore against each other, however, their shapes were modified by wear to produce a precise fit.<ref>{{cite journal |first1=A. W. |last1=Crompton|last2=Jenkins|first2=F. Jr.|year=1968 |title=Molar occlusion in late Triassic mammals |journal=Biological Reviews |volume=43 |issue=4|pages=427–458 |doi=10.1111/j.1469-185x.1968.tb00966.x|pmid=4886687|s2cid=1044399}}</ref> |
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A 2020 study suggests that the metabolism of ''Morganucodon'' was significantly slower than that of comparably sized modern mammals, and that it had a life-span more similar to that of reptiles, with the oldest specimen having a lifespan of 14 years.<ref>{{cite journal |last1= Newham |first1=Elis |last2=Gill |first2=Pamela |display-authors=1 |date=2020 |title=Reptile-like physiology in Early Jurassic stem-mammals |journal=Nature Communications |volume=11 |issue=1 |pages=5121 |doi=10.1038/s41467-020-18898-4 |pmid=33046697 |pmc=7550344 |bibcode=2020NatCo..11.5121N |doi-access=free}}</ref> |
A 2020 study suggests that the metabolism of ''Morganucodon'' was significantly slower than that of comparably sized modern mammals, and that it had a life-span more similar to that of reptiles, with the oldest specimen having a lifespan of 14 years. Thus it likely did not possess the fully [[endotherm]]ic metabolism seen in current mammals.<ref>{{cite journal |last1= Newham |first1=Elis |last2=Gill |first2=Pamela |display-authors=1 |date=2020 |title=Reptile-like physiology in Early Jurassic stem-mammals |journal=Nature Communications |volume=11 |issue=1 |pages=5121 |doi=10.1038/s41467-020-18898-4 |pmid=33046697 |pmc=7550344 |bibcode=2020NatCo..11.5121N |doi-access=free}}</ref> |
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== Species == |
== Species == |
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{{Taxonbar|from=Q131813}} |
{{Taxonbar|from=Q131813}} |
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[[Category: |
[[Category:Morganucodonta]] |
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[[Category:Prehistoric cynodont genera]] |
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[[Category:Late Triassic synapsids]] |
[[Category:Late Triassic synapsids]] |
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[[Category:Triassic synapsids of Europe]] |
[[Category:Triassic synapsids of Europe]] |
Latest revision as of 19:11, 23 September 2024
Morganucodon Temporal range: Late Triassic-Middle Jurassic
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Scan and reconstruction of the M. oehleri holotype skull | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Clade: | Synapsida |
Clade: | Therapsida |
Clade: | Cynodontia |
Clade: | Mammaliaformes |
Order: | †Morganucodonta |
Family: | †Morganucodontidae |
Genus: | †Morganucodon Kühne, 1949 |
Type species | |
†Morganucodon watsoni Kühne, 1949
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Species | |
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Morganucodon ("Glamorgan tooth") is an early mammaliaform genus that lived from the Late Triassic to the Middle Jurassic. It first appeared about 205 million years ago. Unlike many other early mammaliaforms, Morganucodon is well represented by abundant and well preserved (though in the vast majority of cases disarticulated) material. Most of this comes from Glamorgan in Wales (Morganucodon watsoni), but fossils have also been found in Yunnan Province in China (Morganucodon oehleri) and various parts of Europe and North America. Some closely related animals (Megazostrodon) are known from exquisite fossils from South Africa.[1]
The name comes from a Latinization of Morganuc, the name for South Glamorgan in the Domesday Book, the county of Wales where it was discovered by Walter Georg Kühne,[2] giving the meaning "Glamorgan tooth".
History of discovery
[edit]In the summer of 1947, fieldwork was done at Duchy Quarry in Glamorgan in southern Wales. Grey conglomerate that formed fissure fill deposits within karstic voids in Carboniferous limestone was extracted. In 1949, Walter Georg Kühne noted the lower cheek tooth of a primitive mammal while examining samples of the rock. He named it Morganucodon watsoni, with the genus name being derived from Morganuc, which Kühne stated was the name of South Glamorgan in the Domesday Book, with the species name being in honour of D. M. S. Watson.[2] Additional remains of M. watsoni were described by Kühne in 1958.[3] Also in 1958, Kenneth Kermack and Frances Mussett described additional remains from Pant Quarry, about a mile from Duchy Quarry, that had been collected in 1956.[4] In August 1948, an expedition to Lufeng in Yunnan, China yielded a 1 in (2.5 cm) long skull. It was shortly sent to Beijing (then Peking) and then eventually sent out of China, and deposited with Kenneth Kermack at University College London in 1960. The specimen was preliminarily described in 1963 by Harold W. Rigney, who noted the similarity to Morganucodon from Britain, and considered it cogeneric, naming the new species Morganucodon oehleri in honor of the reverend Edgar T. Oehler, who had originally collected the specimen.[5] In 1978 C. C. Young described Eozostrodon heikuopengensis from the Hei Koa Peng locality near Lufeng, based on an associated skull and dentary, as well as a right maxilla and associated dentary.[6] A revision by William A. Clemens in 1979 assigned this species to Morganucodon, based on its close similarity to the two previously named species.[4] In 1980 Clemens named the species Morganucodon peyeri, from isolated teeth found in Late Triassic (Rhaetian) deposits near Hallau, Switzerland, with the species being named after paleontologist Bernhard Peyer.[7] In 1981, Kermack, Mussett and Rigney published an extensive monograph on the skull of Morganucodon.[8] In 2016 Percy Butler and Denise Sigogneau-Russell named the species Morganucodon tardus from an upper right molar (M34984) collected from the Watton Cliff locality near Eype in Dorset, England, dating to the late Bathonian stage of the Middle Jurassic. The species being named after the Latin tardus, late, in reference to it being the youngest member of the genus.[9]
Biology
[edit]Morganucodon was a small, plantigrade animal. The tail was moderately long. According to Kemp (2005), "the skull was 2–3 cm in length and a presacral body length of about 10 cm [4 inches]. In general appearance, it would have looked like a shrew or mouse".[10] There is evidence that it had specialized glands used for grooming, which may indicate that, like present day mammals, it had fur.[11]
Like present day mammals of similar size and presumed habit, Morganucodon was likely nocturnal and spent the day in a burrow. There is no direct fossil evidence, but several lines of evidence point to a nocturnal bottleneck in the evolution of the mammal class, and almost all modern mammals of similar size to Morganucodon are still nocturnal.[12][13] Likewise, burrowing was widespread both in non-mammalian cynodonts and in primitive mammals.[14][15] The logics of phylogenetic bracketing would make Morganucodon nocturnal and burrowing too. Plant material from the conifer Hirmeriella was also found in the fissure fills, indicating Morganucudon lived in, or near, a forested area.
The diet appears to have been insects and other small animals, with a preference for hard prey such as beetles.[16] Like most modern mammal insectivores, it grew fairly quickly to adult size.[17] Its eggs were probably small and leathery, a condition still found in monotremes.[18]
The teeth grew in mammalian fashion, with deciduous teeth being replaced by permanent teeth that were retained throughout the rest of the animal's life.[19] The combination of rapid growth in juveniles and a toothless stage at infancy strongly suggests that Morganucodon raised its young by lactation; indeed, it may have been among the first animals to do so.[20] The molars in the adult had a series of raised humps and edges that fit into each other, allowing for efficient chewing. However, unlike the situation in most later mammals, the upper and lower molars did not occlude properly when they first met; as they wore against each other, however, their shapes were modified by wear to produce a precise fit.[21]
A 2020 study suggests that the metabolism of Morganucodon was significantly slower than that of comparably sized modern mammals, and that it had a life-span more similar to that of reptiles, with the oldest specimen having a lifespan of 14 years. Thus it likely did not possess the fully endothermic metabolism seen in current mammals.[22]
Species
[edit]Species | Author | Year | Status | Temporal range | Location | Formations |
---|---|---|---|---|---|---|
Morganucodon watsoni | Kuehne | 1949 | Early Jurassic (Hettangian-Sinemurian) | England, Wales | Various fissure fill deposits | |
Morganucodon heikuopengensis | Young | 1978 | Early Jurassic (Sinemurian) | Yunnan, China | Lufeng | |
Morganucodon oehleri | Rigney | 1963 | Early Jurassic (Hettangian) | |||
Morganucodon peyeri | Clemens | 1980 | Late Triassic (Rhaetian) | Switzerland, France | Klettgau, grès infraliasiques (Saint-Nicolas-de-Port) | |
Morganucodon tardus | Butler and Sigogneau-Russel | 2016 | Middle Jurassic (Bathonian) | England | Forest Marble |
Classification
[edit]Morganucodon is the type genus for the order Morganucodonta, a group of generally similar mammaliaforms known from the Late Triassic to Late Jurassic epochs,[23][24] with one possible member (Purbeckodon) dating to the Early Cretaceous.[25] All were small and likely insectivorous. Morganucodon is the best preserved and best understood member of Morganucodonta.
There is currently controversy about whether or not to classify Morganucodon as a mammal or as a non-mammalian mammaliaform. Some researchers limit the term "mammal" to the crown group mammals, which would not include Morganucodon and its relatives. Others, however, define "mammals", as a group, by the possession of a special, secondarily evolved jaw joint between the dentary and the squamosal bones, which has replaced the primitive one between the articular and quadrate bones in all modern mammalian groups. Under this definition, Morganucodon would be a mammal. Nevertheless, its lower jaw retains some of the bones found in its non-mammalian ancestors in a very reduced form rather than being composed solely of the dentary. Furthermore, the primitive reptile-like jaw joint between the articular and quadrate bones, which in modern mammals has moved into the middle ear and become part of the ear ossicles as malleus and incus, is still to be found in Morganucodon.[26] Morganucodon also suckled (it may have been the earliest animal to do so), had only two sets of teeth and grew rapidly to adult size and stopped growing thereafter, all typical mammalian traits.[27]
- Phylogeny [28]
See also
[edit]References
[edit]- ^ Pages 21–33, 174 in Zofia Kielan-Jaworowska, Richard L. Cifelli, and Zhe-Xi Luo, Mammals from the Age of Dinosaurs: Origins, Evolution, and Structure, Columbia University Press, New York, 2004 ISBN 0-231-11918-6
- ^ a b Walter G. Kühne, "On a Triconodont tooth of a new pattern from a Fissure-filling in South Glamorgan", Proceedings of the Zoological Society of London, volume 119 (1949–1950) pages 345–350
- ^ Kühne, Walter Georg (1958-08-01). "Rhaetische Triconodonten aus Glamorgan, ihre Stellung zwischen den Klassen Reptilia und Mammalia und ihre Bedeutung für die REICHART'sche Theorie" [Rhaetian triconodonts from Glamorgan, their position between the classes Reptilia and Mammalia and their significance for REICHART's theory.]. Paläontologische Zeitschrift (in German). 32 (3): 197–235. doi:10.1007/BF02989032. ISSN 0031-0220. S2CID 128828761.
- ^ a b Clemens, William A. (May 1979). "A problem in morganucodontid taxonomy (Mammalia)". Zoological Journal of the Linnean Society. 66 (1): 1–14. doi:10.1111/j.1096-3642.1979.tb01898.x.
- ^ Rigney, Harold W. (March 1963). "A Specimen of Morganucodon from Yunnan". Nature. 197 (4872): 1122–1123. Bibcode:1963Natur.197.1122R. doi:10.1038/1971122a0. ISSN 0028-0836. S2CID 4204736.
- ^ C.-C. Young. 1978. New materials of Eozostrodon. Vertebrata PalAsiatica 16:1-3
- ^ W. A. Clemens. 1980. Rhaeto-Liassic mammals from Switzerland and West Germany. Zitteliana 5:51-92
- ^ Kermack, K. A.; Mussett, Frances; Rigney, H. W. (January 1981). "The skull of Morganucodon". Zoological Journal of the Linnean Society. 71 (1): 1–158. doi:10.1111/j.1096-3642.1981.tb01127.x.
- ^ Butler, P.M. and Sigogneau-Russell, D. 2016. Diversity of triconodonts in the Middle Jurassic of Great Britain. Palaeontologia Polonica 67, 35–65. LSID urn:lsid:zoobank.org: pub: C4D90BB6-A001-4DDB-890E-2061B4793992
- ^ Kemp T.S. 2005. The origin and evolution of mammals, Oxford University Press, page 143. ISBN 0-19-850760-7.
- ^ Ruben, J.A.; Jones, T.D. (2000). "Selective Factors Associated with the Origin of Fur and Feathers". American Zoologist. 40 (4): 585–596. doi:10.1093/icb/40.4.585.
- ^ Hall, M. I.; Kamilar, J. M.; Kirk, E. C. (24 October 2012). "Eye shape and the nocturnal bottleneck of mammals". Proceedings of the Royal Society B: Biological Sciences. 279 (1749): 4962–4968. doi:10.1098/rspb.2012.2258. PMC 3497252. PMID 23097513.
- ^ Muchlinski, Magdalena N. (June 2010). "A comparative analysis of vibrissa count and infraorbital foramen area in primates and other mammals". Journal of Human Evolution. 58 (6): 447–473. doi:10.1016/j.jhevol.2010.01.012. PMID 20434193.
- ^ Damiani, R.; Modesto, S.; Yates, A.; Neveling, J. (22 August 2003). "Earliest evidence of cynodont burrowing". Proceedings of the Royal Society B: Biological Sciences. 270 (1525): 1747–1751. doi:10.1098/rspb.2003.2427. PMC 1691433. PMID 12965004.
- ^ KIELAN, ZOFIA; GAMBARYAN, PETR P. (December 1994). "Postcranial anatomy and habits of Asian multituberculate mammals". Lethaia. 27 (4): 300. doi:10.1111/j.1502-3931.1994.tb01578.x. S2CID 85021289.
- ^ Gill, Pamela G.; Purnell, Mark A.; Crumpton, Nick; Robson-Brown, Kate; Gostling, Neil J.; Stampanoni, M.; Rayfield, Emily J. (21 August 2014). "Dietary specializations and diversity in feeding ecology of the earliest stem mammals". Nature. 512 (7514): 303–305. Bibcode:2014Natur.512..303G. doi:10.1038/nature13622. hdl:2381/29192. PMID 25143112. S2CID 4469841.
- ^ Chinsamy, A.; Hurum, J.H. (2006). "Bone microstructure and growth patterns of early mammals" (PDF). Acta Palaeontologica Polonica. 51 (2): 325–338. Retrieved 30 August 2013.
- ^ Parente, Raphael Câmara Medeiros; Bergqvist, Lílian Paglarelli; Soares, Marina Bento; Filho, Olimpio Barbosa Moraes (2011). "The history of vaginal birth". Archives of Gynecology and Obstetrics. 284 (1): 1–11. doi:10.1007/s00404-011-1918-6. PMID 21547459. S2CID 22997887.
- ^ Alexander F. H. van Nievelt and Kathleen K. Smith, "To replace or not to replace: the significance of reduced functional tooth replacement in marsupial and placental mammals", Paleobiology, Volume 31, Issue 2 (June 2005) pages 324–346
- ^ Kielan-Jaworowska, Zofia; Cifelli, Richard L.; Luo, Zhe-Xi (2004). Mammals from the age of dinosaurs : origins, evolution, and structure. New York: Columbia University Press. pp. 148–153. ISBN 978-0231119184.
- ^ Crompton, A. W.; Jenkins, F. Jr. (1968). "Molar occlusion in late Triassic mammals". Biological Reviews. 43 (4): 427–458. doi:10.1111/j.1469-185x.1968.tb00966.x. PMID 4886687. S2CID 1044399.
- ^ Newham, Elis; et al. (2020). "Reptile-like physiology in Early Jurassic stem-mammals". Nature Communications. 11 (1): 5121. Bibcode:2020NatCo..11.5121N. doi:10.1038/s41467-020-18898-4. PMC 7550344. PMID 33046697.
- ^ Martin, T.; Averianov, A. O.; Jäger, K. R. K.; Schwermann, A. H.; Wings, O. (2019). "A large morganucodontan mammaliaform from the Late Jurassic of Germany" (PDF). Fossil Imprint. 75 (3–4): 504–509. doi:10.2478/if-2019-0030.
- ^ pages 511–512, Malcolm C. McKenna and Susan K. Bell, Classification of Mammals Above the Species Level, Columbia University Press, 1997. ISBN 0-231-11012-X
- ^ P. M. Butler, D. Sigogneau-Russell and P. C. Ensom (2011). "Possible persistence of the morganucodontans in the Lower Cretaceous Purbeck Limestone Group (Dorset, England)". Cretaceous Research. 33: 135–145. doi:10.1016/j.cretres.2011.09.007.
- ^ Kermack, K. A.; Mussett, Frances; Rigney, H. W. (1981). "The skull of Morganucodon". Zoological Journal of the Linnean Society. 71: 1–158. doi:10.1111/j.1096-3642.1981.tb01127.x.
- ^ Mammals of the Mesozoic: The least mammal-like mammals
- ^ Close, Roger A.; Friedman, Matt; Lloyd, Graeme T.; Benson, Roger BJ (2015). "Evidence for a mid-Jurassic adaptive radiation in mammals". Current Biology. 25 (16): 2137–2142. doi:10.1016/j.cub.2015.06.047. PMID 26190074.