Pierolapithecus: Difference between revisions
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{{short description|Extinct species of ape from Miocene Europe}} |
{{short description|Extinct species of ape from Miocene Europe}} |
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{{Speciesbox |
{{Speciesbox |
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| fossil_range = [[Miocene]], {{fossilrange|13}} |
| fossil_range = [[Miocene]], {{fossilrange|12.5|13}} |
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| image = Pierolapithecus catalaunicus (Kopie).jpg |
| image = Pierolapithecus catalaunicus (Kopie).jpg |
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| image_alt = Reconstruction of "Pierolapithecus catalaunicus" |
| image_alt = Reconstruction of "Pierolapithecus catalaunicus" |
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'''''Pierolapithecus catalaunicus''''' is an extinct species of [[primate]] which lived |
'''''Pierolapithecus catalaunicus''''' is an extinct species of [[primate]] which lived around 12.5-13 million years ago during the [[Miocene]] in what is now [[Hostalets de Pierola]], [[Catalonia]], [[Spain]]. Some researchers believe that it is a candidate for [[common ancestor]] to the [[great ape]] clade, or is at least closer than any previous fossil discovery.<ref>{{Cite web | title = 'Original' great ape discovered | url = http://news.bbc.co.uk/1/hi/sci/tech/4014351.stm | first = Paul | last = Rincon | publisher = BBC | date = 18 November 2004 | access-date = 23 January 2013}}</ref> Others suggest it being a [[Ponginae|pongine]],<ref name="Pérez de los Ríos-2012" /> or a [[Dryopithecini|dryopith]].<ref name="Sevim-Erol-2023" /> On 16 October 2023, scientists reported the facial reconstruction of the great ape.<ref name="Johnson">{{cite news |last=Johnson |first=Mark |title=Scientists reconstructed the face of a 12 million-year-old great ape - Fossils of the extinct species Pierolapithecus catalaunicus may reveal clues about our origins |url=https://www.washingtonpost.com/science/2023/10/24/ancient-ape-face-reconstructed-fossils-landfill/ |date=24 October 2023 |newspaper=[[The Washington Post]] |url-status=live |archiveurl=https://archive.today/20231024143144/https://www.washingtonpost.com/science/2023/10/24/ancient-ape-face-reconstructed-fossils-landfill/ |archivedate=24 October 2023 |accessdate=25 October 2023 }}</ref><ref name="Pugh">{{cite journal |author=Pugh, Kelsey D. |display-authors=et al. |title=The reconstructed cranium of Pierolapithecus and the evolution of the great ape face |date=16 October 2023 |journal=[[Proceedings of the National Academy of Sciences of the United States of America|PNAS]] |volume=120 |issue=44 |pages=e2218778120 |doi=10.1073/pnas.2218778120 |pmid=37844214 |doi-access=free |pmc=10622906 |bibcode=2023PNAS..12018778P }}</ref> |
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== History == |
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The species was described by a team of Spanish [[paleoanthropologist]]s led by [[Salvador Moyà-Solà]] on the basis of a [[fossil]] specimen discovered in December 2002. The finding was first reported in the [[Academic journal|journal]] [[Science (journal)|Science]] on November 19, 2004.<ref name="MoyaSola2004">{{Cite journal | last1 = Moya-Sola | first1 = S. | last2 = Köhler | first2 = M. | last3 = Alba | first3 = D. M. | last4 = Casanovas-Vilar | first4 = I. | last5 = Galindo | first5 = J. | title = ''Pierolapithecus catalaunicus'', a New Middle Miocene Great Ape from Spain | doi = 10.1126/science.1103094 | journal = Science | volume = 306 | issue = 5700 | pages = 1339–1344 | year = 2004 | pmid = 15550663| bibcode = 2004Sci...306.1339M | s2cid = 129576842 | url = http://doc.rero.ch/record/14752/files/PAL_E1879.pdf }}</ref> |
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The [[splanchnocranium]] was discovered in 2002 and systematic excavations took place during May and June 2003.<ref name="Casanovasvilar-2008">{{Cite journal |last1=Casanovasvilar |first1=I |last2=Alba |first2=D |last3=Moyasola |first3=S |last4=Galindo |first4=J |last5=Cabrera |first5=L |last6=Garces |first6=M |last7=Furio |first7=M |last8=Robles |first8=J |last9=Kohler |first9=M |last10=Angelone |first10=C |date=2008 |title=Biochronological, taphonomical, and paleoenvironmental background of the fossil great ape Pierolapithecus catalaunicus (Primates, Hominidae) |url=https://linkinghub.elsevier.com/retrieve/pii/S0047248408000948 |journal=Journal of Human Evolution |language=en |volume=55 |issue=4 |pages=589–603 |doi=10.1016/j.jhevol.2008.05.004|pmid=18691737 |bibcode=2008JHumE..55..589C }}</ref> The species was described by a team of Spanish [[paleoanthropologist]]s led by [[Salvador Moyà-Solà]] on the basis of a [[fossil]] skeleton, '''IPS21350''' (nicknamed '''Pau''' ("peace" in Catalan as it was announced alongside Spanish demonstrations against the [[Iraq War]])<ref name="Bezanson-2016">{{Cite book |url=https://onlinelibrary.wiley.com/doi/book/10.1002/9781119179313 |title=The International Encyclopedia of Primatology |date=2016-06-14 |publisher=Wiley |isbn=978-0-470-67337-9 |editor-last=Bezanson |editor-first=Michele |edition=1 |language=en |doi=10.1002/9781119179313.wbprim0216 |editor-last2=MacKinnon |editor-first2=Katherine C |editor-last3=Riley |editor-first3=Erin |editor-last4=Campbell |editor-first4=Christina J |editor-last5=Nekaris |editor-first5=K.A.I (Anna) |editor-last6=Estrada |editor-first6=Alejandro |editor-last7=Di Fiore |editor-first7=Anthony F |editor-last8=Ross |editor-first8=Stephen |editor-last9=Jones-Engel |editor-first9=Lisa E}}</ref>), discovered in December 2002. The finding was first reported in the [[Academic journal|journal]] [[Science (journal)|''Science'']] on November 19, 2004. The skeleton is of an adult male individual, composed of 83 bones that make up the splanchnocranium, both [[Maxilla|maxillae]], a complete set of cheek teeth, both canines, a right central incisor, [[Zygomatic bone|zygomatics]], [[Lacrimal bone|lacrimals]], a partial [[Frontal bone|frontal]], [[Carpal bones|carpals]], [[Metacarpal bones|metacarpals]], [[Phalanges|manual phalanges]] from two hands, [[Tarsus (skeleton)|tarsals]], [[Metatarsal bones|metatarsals]], pedal phalanges, right [[Patella|patellar]] distal [[epiphysis]], a left [[Radius (bone)|radius]], some long bone [[Diaphysis|diaphyses]], two pelvic pieces, three vertebrae, two intact ribs, and twelve rib fragments of large size. They named their new genus after the nearby village Els Hostalets de Pierola, and Catalonia respectively.<ref name="MoyaSola2004">{{Cite journal |last1=Moya-Sola |first1=S. |last2=Köhler |first2=M. |last3=Alba |first3=D. M. |last4=Casanovas-Vilar |first4=I. |last5=Galindo |first5=J. |year=2004 |title=''Pierolapithecus catalaunicus'', a New Middle Miocene Great Ape from Spain |url=http://doc.rero.ch/record/14752/files/PAL_E1879.pdf |journal=Science |volume=306 |issue=5700 |pages=1339–1344 |bibcode=2004Sci...306.1339M |doi=10.1126/science.1103094 |pmid=15550663 |s2cid=129576842}}</ref> |
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== Description == |
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As do humans and other great [[ape]]s, ''Pierolapithecus'' had specialized adaptations for tree climbing: a wide, flat ribcage, a stiff lower spine, flexible wrists, and shoulder blades that lay along its back. It also has [[Symplesiomorphy|plesiomorphic]] monkey-like features such as a sloped face and short fingers and toes.<ref name="MoyaSola2004" /> ([[gibbon]]s and [[Old World monkey]]s show more generalized characteristics.) |
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Moyà-Solà ''et al.'' initially founded the species on a set of unique characteristics, of which are the following. The frontal processes of the face remain on the same plane, the [[Nasal bone|nasals]] are flat and sit beneath the lower rims of the [[Orbit (anatomy)|orbit]], the [[glabella]] is posteriorly oriented, the face is low, the brows are thin, the zygomatic root is high, and the [[nasoalveolar clivus]] is high. The rear border of the [[incisive foramen]] is in line with the P3, the [[palate]] is deep and stout, the [[Nasal cavity|nasal aperture]] is widest at the base, the [[interorbital distance]] is wide, the zygomatics expand to the side, the P3 is similar in size to the P4, there is reduced cusp heteromorphy, all molars save from the M3 are elongated, the upper molars and premolars lack cingula, the lingual cusps of the upper molars are positioned peripherally, the M2 is large and has cusp heteromorphy, and the upper canine is large and compressed in the crown. The ribs are very curved to form a [[thorax]] that is anteroposteriorly compressed, the [[clavicle]] is robust, lacking a ventral keel on the mid-[[Lumbar vertebrae|lumbars]], the [[Pedicles of the vertebral arches|pedicles]] of the neural arch are robust and stout, the [[spinous processes]] are slightly caudally inclined, the pedicle-body inserts the [[transverse processes]], dorsally oriented and pedicle-born transverse process, the metacarpals and phalanges are short, the [[Accessory bone|os centrale]] are unfused, the [[Triquetral bone|triquetrum]] is small and non-articulating with the [[Ulnar styloid process|ulnar styloid]], and the crevice inserting [[Meniscus (anatomy)|meniscus]] attachment and [[pisiform facet]] is distally shifted.<ref name="MoyaSola2004" /> |
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The holotypic individual is estimated to have weighed 30 kg (66.13 lbs).<ref name="Bezanson-2016" /> |
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⚫ | That ''Pierolapithecus'' would be ancestral to modern great apes is debated largely because this great ape was found in the [[Iberian Peninsula]], while most of the fossil evidence of the evolution of |
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== Locomotion == |
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Rather than a full common ancestor, it has been suggested that the species may be ancestral to humans, [[chimpanzee]]s and [[gorilla]]s but not [[orangutan]]s, given certain characteristics of the face. <ref name="Begun2015">{{cite book |last1=Begun |first1=D. R. |title=Fossil record of Miocene hominoids. |date=2015 |publisher=Springer |location=Berlin |isbn=978-3-642-39980-0 |pages=1304–1306 |edition=2nd |ref=3}}</ref> |
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Overall, the [[adduction]] and [[supination]] capacity of the wrist, specially built thorax, [[Scapula|scapular]] shift to the back (which was inferred through the long, [[chimpanzee]]-like clavicles), and stiff lumbar vertebrae suggest that positional behavior and [[Orthograde posture|orthograde]] locomotion were emphasized. This type of movement is diagnostic for all extant [[ape]]s including [[human]]s, but it is rarely documented in the fossil record. Other hominids that have this suite are ''[[Oreopithecus]]'' and, although less skeletally complete, ''[[Dryopithecus]]''. Earlier taxa—''[[Proconsul]]'', ''[[Afropithecus]]'', ''[[Equatorius]]'', ''[[Nacholapithecus]]''—retain basal characters and the similarly-aged ''[[Morotopithecus]]'' practiced orthograde locomotion but was probably sister to apes (based on facial structure). The shortened phalanges suggest ancestral [[palmigrade]] adaptations, but it is unlikely ''Pierolapithecus'' practiced much or any [[Suspensory behavior|suspensory]] behavior. However, vertical climbing and suspension are independent abilities that are integral to ape evolution. Below-branch suspension may have evolved repeatedly or in [[Convergent evolution|convergence]] later and independently in the ape lineage.<ref name="MoyaSola2004" /> |
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[[File:Pierolapithecus patella.png|thumb|248x248px|Patella of the holotype ''P. catalaunicus'']] |
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Further analysis suggests that very long and curved phalanges is decoupled with orthograde features related to vertical climbing being acquired. The condition in this [[genus]] is related to a retained [[pronograde]] plan. Although the lumbars, ribs, and carpals are orthograde, the degree of this in the phalanges is only slight. Many traits were independently acquired, leading to new advances being superimposed and basal characters retained for an extended time. ''Pierolapithecus'' lacked adaptations for suspensory hanging, but it may have still been capable of doing so, only that it was not adaptively relevant.<ref name="Almécija-2009">{{Cite journal |last1=Almécija |first1=Sergio |last2=Alba |first2=David M. |last3=Moyà-Solà |first3=Salvador |date=2009 |title=Pierolapithecus and the functional morphology of Miocene ape hand phalanges: paleobiological and evolutionary implications |url=https://linkinghub.elsevier.com/retrieve/pii/S0047248409000554 |journal=Journal of Human Evolution |language=en |volume=57 |issue=3 |pages=284–297 |doi=10.1016/j.jhevol.2009.02.008|pmid=19631964 |bibcode=2009JHumE..57..284A }}</ref> Although, the latter remains disputed.<ref>{{Cite journal |last1=Alba |first1=David M. |last2=Almécija |first2=Sergio |last3=Moyà-Solà |first3=Salvador |date=2010-07-01 |title=Locomotor inferences in Pierolapithecus and Hispanopithecus: Reply to Deane and Begun (2008) |url=https://www.sciencedirect.com/science/article/pii/S0047248410000266 |journal=Journal of Human Evolution |volume=59 |issue=1 |pages=143–149 |doi=10.1016/j.jhevol.2010.02.002 |pmid=20510436 |bibcode=2010JHumE..59..143A |issn=0047-2484}}</ref> |
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The patella was like extant apes in dimensions, which is typically regarded as having a mobile knee. ''Pierolapithecus'' differs from monkeys, [[hylobatid]]s, and basal [[hominoid]]s through thicker patellae. As such, a derived knee might be related to enhanced climbing, notably vertical climbing.<ref>{{Cite journal |last1=Pina |first1=Marta |last2=Almécija |first2=Sergio |last3=Alba |first3=David M. |last4=O'Neill |first4=Matthew C. |last5=Moyà-Solà |first5=Salvador |date=2014 |title=The Middle Miocene Ape Pierolapithecus catalaunicus Exhibits Extant Great Ape-Like Morphometric Affinities on Its Patella: Inferences on Knee Function and Evolution |journal=PLOS ONE |language=en |volume=9 |issue=3 |pages=e91944 |doi=10.1371/journal.pone.0091944 |issn=1932-6203 |pmc=3956854 |pmid=24637777 |bibcode=2014PLoSO...991944P |doi-access=free }}</ref> The pelvis shares an ancestral template with ''Proconsul nyanzae'', which was modified for orthograde behavior (assuming that hypothesis is accepted), and suggests [[homoplasy]] in ape pelves.<ref>{{Cite journal |last1=Hammond |first1=Ashley S. |last2=Alba |first2=David M. |last3=Almécija |first3=Sergio |last4=Moyà-Solà |first4=Salvador |date=2013 |title=Middle Miocene Pierolapithecus provides a first glimpse into early hominid pelvic morphology |url=https://linkinghub.elsevier.com/retrieve/pii/S0047248413000742 |journal=Journal of Human Evolution |language=en |volume=64 |issue=6 |pages=658–666 |doi=10.1016/j.jhevol.2013.03.002|pmid=23545221 |bibcode=2013JHumE..64..658H }}</ref> |
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== Classification == |
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''Pierolapithecus'' demonstrates derived facial features and apelike skeletal adaptations that suggest that it is an early member of the ape [[clade]]. This genus, 12.5-13 mya in age, postdates the hylobatid-[[Hominidae|hominid]] split, which occurred anywhere from 14.9±2 or 14.6±2.6 mya. Much of the skeleton is derived, but the shortened phalanges are indicative of palmigrade adaptations that are primitive. This mosaic is important in ape evolution.<ref name="MoyaSola2004" /> The large amount of homoplasy in ape locomotion creates considerable [[Taxonomy (biology)|taxonomic]] confusion. The late [[Middle Miocene]] is the farthest trace of a ''Pierolapithecus''-like character group, and assuming that this identifies the earliest apes, is the farthest trace of hominids. As well, early hominids are substantially more primitive than estimated, which may explain why no early great apes were previously reported.<ref name="MoyaSola2004" /> These early traits would have been maintained, overlaid, and modified to suite new adaptations that occurred independently.<ref name="Almécija-2009" /> |
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''Pierolapithecus'' and ''[[Anoiapithecus]]'' may be synonymous with ''Dryopithecus'',<ref name="Begun2015"/> but both have enough craniofacial differences to justify separation.<ref name="Alba-2010"/> Placement as a basal hominid is supported by the comparison of the thick enamel from the [[Afropithecidae|afropithecids]], which may be ancestral to apes.<ref name="Alba-2010">{{Cite journal |last1=Alba |first1=D. M. |last2=Fortuny |first2=J. |last3=Moyà-Solà |first3=S. |date=2010 |title=Enamel thickness in the Middle Miocene great apes Anoiapithecus , Pierolapithecus and Dryopithecus |journal=Proceedings of the Royal Society B: Biological Sciences |language=en |volume=277 |issue=1691 |pages=2237–2245 |doi=10.1098/rspb.2010.0218 |issn=0962-8452 |pmc=2880156 |pmid=20335211}}</ref> Other hypotheses are that the taxon represents a stem pongine.<ref name="Pérez de los Ríos-2012">{{Cite journal |last1=Pérez de los Ríos |first1=Miriam |last2=Moyà-Solà |first2=Salvador |last3=Alba |first3=David M. |date=2012-09-01 |title=The nasal and paranasal architecture of the Middle Miocene ape Pierolapithecus catalaunicus (primates: Hominidae): Phylogenetic implications |url=https://www.sciencedirect.com/science/article/pii/S0047248412000978 |journal=Journal of Human Evolution |volume=63 |issue=3 |pages=497–506 |doi=10.1016/j.jhevol.2012.05.012 |pmid=22819226 |bibcode=2012JHumE..63..497P |issn=0047-2484}}</ref> Rather than a full common ancestor, it has been suggested that the species may be ancestral to humans, chimpanzees and [[gorilla]]s but not [[orangutan]]s, given certain facial characteristics.<ref name="Begun2015">{{cite book |last1=Begun |first1=D. R. |title=Fossil record of Miocene hominoids. |date=2015 |publisher=Springer |isbn=978-3-642-39980-0 |edition=2nd |location=Berlin |pages=1304–1306 |ref=3}}</ref> This genus is distinguished from pongines and share traits with extant [[Homininae|hominines]], suggesting a sister relationship with ''Dryopithecus'' (possibly in a tribe called Dryopithecini, having thick and thin enamel much like ''[[Ardipithecus]]''/[[Australopithecine|australopiths]] and ''[[Pan (genus)|Pan]]''/hominins).<ref name="Sevim-Erol-2023">{{Cite journal |last1=Sevim-Erol |first1=Ayla |last2=Begun |first2=D. R. |last3=Sözer |first3=Ç Sönmez |last4=Mayda |first4=S. |last5=van den Hoek Ostende |first5=L. W. |last6=Martin |first6=R. M. G. |last7=Alçiçek |first7=M. Cihat |date=2023-08-23 |title=A new ape from Türkiye and the radiation of late Miocene hominines |journal=Communications Biology |language=en |volume=6 |issue=1 |page=842 |doi=10.1038/s42003-023-05210-5 |issn=2399-3642 |pmc=10447513 |pmid=37612372}}</ref> A reconstruction of the face of ''Pierolapithecus catalaunicus'' indicates its morphology as most consistent with a phylogenetic placement as a [[Crown group#Stem groups|stem]] [[Hominidae|hominid]].<ref>{{Cite journal|last1=Pugh |first1=K. D. |last2=Catalano |first2=S. A. |last3=Pérez de los Ríos |first3=M. |last4=Fortuny |first4=J. |last5=Shearer |first5=B. M. |last6=Vecino Gazabón |first6=A. |last7=Hammond |first7=A. S. |last8=Moyà-Solà |first8=S. |last9=Alba |first9=D. M. |last10=Almécija |first10=S. |year=2023 |title=The reconstructed cranium of ''Pierolapithecus'' and the evolution of the great ape face |journal=Proceedings of the National Academy of Sciences of the United States of America |volume=120 |issue=44 |at=e2218778120 |doi=10.1073/pnas.2218778120 |pmid=37844214 |pmc=10622906 |bibcode=2023PNAS..12018778P }}</ref> |
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== Paleoecology == |
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''Pierolapithecus'' bore thick enamel found in hard-object feeders, but its diet is not yet known aside from possibly having fed in trees like orangutans.<ref name="Bezanson-2016" /><ref name="Alba-2010" /> It was discovered at the locality of BCV1,<ref>{{cite journal| last1=Hammond |first1=AS |last2=Alba |first2=DM |last3=Almécija |first3=S |last4=Moyà-Solà |first4=S |year=2013 |title=Middle Miocene hominid ''Pierolapithecus'' provides insight into early hominid pelvic morphology |journal=Paleoanthropology |volume=2013 |issue=2013 |page=A16 |url=https://paleoanthropology.org/ojs/index.php/paleo/article/view/706/667 |issn=1545-0031}}</ref> which formed when the northwestern [[Mediterranean Sea|Mediterranean]] rifted to form a stretch between two mountain ranges. The proximal to distal-marginal [[Alluvium|alluvial]]-fan sediments cover the Miocene. It was discovered as a fossiliferous area by Guerín in the 1920s with an ape M2 mistaken as a [[Suidae|suid]], followed by the discovery of ''Dryopithecus fontani'', ''[[Hispanopithecus laietanus]]'', and ''[[Sivapithecus|Sivapithecus occidentalis]]'' in the area. From the area hailing ''Pierolapithecus'' specifically was explored from the 1950s–1970s from a garbage dump. 19 large and small mammals were discovered at the site, almost 300 [[macroinvertebrate]] fossils, and 83 hominid fossils (composing the holotype skeleton).<ref name="Casanovasvilar-2008" /> |
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The [[fauna]] comprises the ''Pierolapithecus'', [[Megaherbivore|megaherbivores]] like elephants, and various others like carnivores, [[Artiodactyl|artiodactyls]], turtles, and small-medium fragments. ''Pierolapithecus'' bears evidence of scavenging whereas the other fossils show signs of being scattered across an alluvial plain. The [[micromammals]] show signs of [[digestion]] by predators, probably by barn owls and others. The environment was quite humid, warm, and forested. The fauna is most like [[France]] and [[central Europe]] in composition. More [[Insectivore|insectivores]], arboreal [[Dormouse|dormice]], and [[Flying squirrel|flying squirrels]] support a humid environment, and the open woodlands of other sites would have made hominid occupation impossible.<ref name="Casanovasvilar-2008" /> |
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⚫ | That ''Pierolapithecus'' would be ancestral to modern great apes is debated largely because this great ape was found in the [[Iberian Peninsula]], while most of the fossil evidence of the evolution of hominids and hominins has been located in [[East Africa]] and [[Southeast Asia]]. Because the Mediterranean Sea contracted several times in the past, migration of terrestrial fauna between [[Africa]] and [[Europe]] was permitted.<ref>{{cite journal |last1=Roegl |first1=Fred |date=1999 |title=Mediterranean and Paratethys. Facts and hypotheses of an Oligocene to Miocene paleogeography (short overview) |journal=Geol. Carpathica |volume=50 |pages=339–349}}</ref> |
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''Pierolapithecus'', like many other Miocene apes, is predicted to have been [[Polygyny|polygynous]] by its low second-to-fourth digit ratios, which are reflective of high prenatal androgen effects and correlated with polygyny in apes.<ref>{{Cite journal |last=Nelson |first=Emma |last2=Rolian |first2=Campbell |last3=Cashmore |first3=Lisa |last4=Shultz |first4=Susanne |date=3 November 2010 |title=Digit ratios predict polygyny in early apes, Ardipithecus , Neanderthals and early modern humans but not in Australopithecus |url=https://royalsocietypublishing.org/doi/10.1098/rspb.2010.1740 |journal=[[Proceedings of the Royal Society B: Biological Sciences]] |language=en |volume=278 |issue=1711 |pages=1556–1563 |doi=10.1098/rspb.2010.1740 |issn=0962-8452 |pmc=3081742 |pmid=21047863 |access-date=10 July 2024}}</ref> |
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== See also == |
== See also == |
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{{Portal|Paleontology |
{{Portal|Paleontology|Primates |
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{{div col}} |
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{{columnslist|colwidth=25em| |
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* {{annotated link|Anoiapithecus|''Anoiapithecus''}} |
* {{annotated link|Anoiapithecus|''Anoiapithecus''}} |
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* {{annotated link|Chororapithecus|''Chororapithecus''}} |
* {{annotated link|Chororapithecus|''Chororapithecus''}} |
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* {{annotated link|Griphopithecus|''Griphopithecus''}} |
* {{annotated link|Griphopithecus|''Griphopithecus''}} |
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* {{annotated link|Nakalipithecus|''Nakalipithecus''}} |
* {{annotated link|Nakalipithecus|''Nakalipithecus''}} |
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* {{annotated link|Samburupithecus|''Samburupithecus''}} |
* {{annotated link|Samburupithecus|''Samburupithecus''}} |
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}} |
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{{div col end}} |
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==References== |
==References== |
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{{Haplorhini|Ho.}} |
{{Haplorhini|Ho.}} |
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{{Taxonbar|from1= |
{{Taxonbar|from1=Q21446402|from2=Q132728}} |
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[[Category:Hominidae]] |
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[[Category:Prehistoric mammals of Europe]] |
[[Category:Prehistoric mammals of Europe]] |
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[[Category:Prehistoric apes]] |
[[Category:Prehistoric apes]] |
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[[Category:Transitional fossils]] |
[[Category:Transitional fossils]] |
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[[Category:Fossil taxa described in 2004]] |
[[Category:Fossil taxa described in 2004]] |
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[[Category: |
[[Category:Monotypic prehistoric primate genera]] |
Latest revision as of 18:48, 6 November 2024
Pierolapithecus Temporal range: Miocene,
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Pierolapithecus catalaunicus | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Chordata |
Class: | Mammalia |
Order: | Primates |
Suborder: | Haplorhini |
Infraorder: | Simiiformes |
Family: | Hominidae |
Subfamily: | incertae sedis |
Genus: | †Pierolapithecus Moyà-Solà et al., 2004 |
Species: | †P. catalaunicus
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Binomial name | |
†Pierolapithecus catalaunicus |
Pierolapithecus catalaunicus is an extinct species of primate which lived around 12.5-13 million years ago during the Miocene in what is now Hostalets de Pierola, Catalonia, Spain. Some researchers believe that it is a candidate for common ancestor to the great ape clade, or is at least closer than any previous fossil discovery.[1] Others suggest it being a pongine,[2] or a dryopith.[3] On 16 October 2023, scientists reported the facial reconstruction of the great ape.[4][5]
History
[edit]The splanchnocranium was discovered in 2002 and systematic excavations took place during May and June 2003.[6] The species was described by a team of Spanish paleoanthropologists led by Salvador Moyà-Solà on the basis of a fossil skeleton, IPS21350 (nicknamed Pau ("peace" in Catalan as it was announced alongside Spanish demonstrations against the Iraq War)[7]), discovered in December 2002. The finding was first reported in the journal Science on November 19, 2004. The skeleton is of an adult male individual, composed of 83 bones that make up the splanchnocranium, both maxillae, a complete set of cheek teeth, both canines, a right central incisor, zygomatics, lacrimals, a partial frontal, carpals, metacarpals, manual phalanges from two hands, tarsals, metatarsals, pedal phalanges, right patellar distal epiphysis, a left radius, some long bone diaphyses, two pelvic pieces, three vertebrae, two intact ribs, and twelve rib fragments of large size. They named their new genus after the nearby village Els Hostalets de Pierola, and Catalonia respectively.[8]
Description
[edit]Moyà-Solà et al. initially founded the species on a set of unique characteristics, of which are the following. The frontal processes of the face remain on the same plane, the nasals are flat and sit beneath the lower rims of the orbit, the glabella is posteriorly oriented, the face is low, the brows are thin, the zygomatic root is high, and the nasoalveolar clivus is high. The rear border of the incisive foramen is in line with the P3, the palate is deep and stout, the nasal aperture is widest at the base, the interorbital distance is wide, the zygomatics expand to the side, the P3 is similar in size to the P4, there is reduced cusp heteromorphy, all molars save from the M3 are elongated, the upper molars and premolars lack cingula, the lingual cusps of the upper molars are positioned peripherally, the M2 is large and has cusp heteromorphy, and the upper canine is large and compressed in the crown. The ribs are very curved to form a thorax that is anteroposteriorly compressed, the clavicle is robust, lacking a ventral keel on the mid-lumbars, the pedicles of the neural arch are robust and stout, the spinous processes are slightly caudally inclined, the pedicle-body inserts the transverse processes, dorsally oriented and pedicle-born transverse process, the metacarpals and phalanges are short, the os centrale are unfused, the triquetrum is small and non-articulating with the ulnar styloid, and the crevice inserting meniscus attachment and pisiform facet is distally shifted.[8]
The holotypic individual is estimated to have weighed 30 kg (66.13 lbs).[7]
Locomotion
[edit]Overall, the adduction and supination capacity of the wrist, specially built thorax, scapular shift to the back (which was inferred through the long, chimpanzee-like clavicles), and stiff lumbar vertebrae suggest that positional behavior and orthograde locomotion were emphasized. This type of movement is diagnostic for all extant apes including humans, but it is rarely documented in the fossil record. Other hominids that have this suite are Oreopithecus and, although less skeletally complete, Dryopithecus. Earlier taxa—Proconsul, Afropithecus, Equatorius, Nacholapithecus—retain basal characters and the similarly-aged Morotopithecus practiced orthograde locomotion but was probably sister to apes (based on facial structure). The shortened phalanges suggest ancestral palmigrade adaptations, but it is unlikely Pierolapithecus practiced much or any suspensory behavior. However, vertical climbing and suspension are independent abilities that are integral to ape evolution. Below-branch suspension may have evolved repeatedly or in convergence later and independently in the ape lineage.[8]
Further analysis suggests that very long and curved phalanges is decoupled with orthograde features related to vertical climbing being acquired. The condition in this genus is related to a retained pronograde plan. Although the lumbars, ribs, and carpals are orthograde, the degree of this in the phalanges is only slight. Many traits were independently acquired, leading to new advances being superimposed and basal characters retained for an extended time. Pierolapithecus lacked adaptations for suspensory hanging, but it may have still been capable of doing so, only that it was not adaptively relevant.[9] Although, the latter remains disputed.[10]
The patella was like extant apes in dimensions, which is typically regarded as having a mobile knee. Pierolapithecus differs from monkeys, hylobatids, and basal hominoids through thicker patellae. As such, a derived knee might be related to enhanced climbing, notably vertical climbing.[11] The pelvis shares an ancestral template with Proconsul nyanzae, which was modified for orthograde behavior (assuming that hypothesis is accepted), and suggests homoplasy in ape pelves.[12]
Classification
[edit]Pierolapithecus demonstrates derived facial features and apelike skeletal adaptations that suggest that it is an early member of the ape clade. This genus, 12.5-13 mya in age, postdates the hylobatid-hominid split, which occurred anywhere from 14.9±2 or 14.6±2.6 mya. Much of the skeleton is derived, but the shortened phalanges are indicative of palmigrade adaptations that are primitive. This mosaic is important in ape evolution.[8] The large amount of homoplasy in ape locomotion creates considerable taxonomic confusion. The late Middle Miocene is the farthest trace of a Pierolapithecus-like character group, and assuming that this identifies the earliest apes, is the farthest trace of hominids. As well, early hominids are substantially more primitive than estimated, which may explain why no early great apes were previously reported.[8] These early traits would have been maintained, overlaid, and modified to suite new adaptations that occurred independently.[9]
Pierolapithecus and Anoiapithecus may be synonymous with Dryopithecus,[13] but both have enough craniofacial differences to justify separation.[14] Placement as a basal hominid is supported by the comparison of the thick enamel from the afropithecids, which may be ancestral to apes.[14] Other hypotheses are that the taxon represents a stem pongine.[2] Rather than a full common ancestor, it has been suggested that the species may be ancestral to humans, chimpanzees and gorillas but not orangutans, given certain facial characteristics.[13] This genus is distinguished from pongines and share traits with extant hominines, suggesting a sister relationship with Dryopithecus (possibly in a tribe called Dryopithecini, having thick and thin enamel much like Ardipithecus/australopiths and Pan/hominins).[3] A reconstruction of the face of Pierolapithecus catalaunicus indicates its morphology as most consistent with a phylogenetic placement as a stem hominid.[15]
Paleoecology
[edit]Pierolapithecus bore thick enamel found in hard-object feeders, but its diet is not yet known aside from possibly having fed in trees like orangutans.[7][14] It was discovered at the locality of BCV1,[16] which formed when the northwestern Mediterranean rifted to form a stretch between two mountain ranges. The proximal to distal-marginal alluvial-fan sediments cover the Miocene. It was discovered as a fossiliferous area by Guerín in the 1920s with an ape M2 mistaken as a suid, followed by the discovery of Dryopithecus fontani, Hispanopithecus laietanus, and Sivapithecus occidentalis in the area. From the area hailing Pierolapithecus specifically was explored from the 1950s–1970s from a garbage dump. 19 large and small mammals were discovered at the site, almost 300 macroinvertebrate fossils, and 83 hominid fossils (composing the holotype skeleton).[6]
The fauna comprises the Pierolapithecus, megaherbivores like elephants, and various others like carnivores, artiodactyls, turtles, and small-medium fragments. Pierolapithecus bears evidence of scavenging whereas the other fossils show signs of being scattered across an alluvial plain. The micromammals show signs of digestion by predators, probably by barn owls and others. The environment was quite humid, warm, and forested. The fauna is most like France and central Europe in composition. More insectivores, arboreal dormice, and flying squirrels support a humid environment, and the open woodlands of other sites would have made hominid occupation impossible.[6]
That Pierolapithecus would be ancestral to modern great apes is debated largely because this great ape was found in the Iberian Peninsula, while most of the fossil evidence of the evolution of hominids and hominins has been located in East Africa and Southeast Asia. Because the Mediterranean Sea contracted several times in the past, migration of terrestrial fauna between Africa and Europe was permitted.[17]
Pierolapithecus, like many other Miocene apes, is predicted to have been polygynous by its low second-to-fourth digit ratios, which are reflective of high prenatal androgen effects and correlated with polygyny in apes.[18]
See also
[edit]- Anoiapithecus – Extinct genus of ape from the Miocene
- Chororapithecus – Extinct hominine genus from the Miocene
- Griphopithecus – Extinct genus of primates
- Nakalipithecus – Extinct species of ape
- Samburupithecus – Extinct genus of primate from Miocene Kenya
References
[edit]- ^ Rincon, Paul (18 November 2004). "'Original' great ape discovered". BBC. Retrieved 23 January 2013.
- ^ a b Pérez de los Ríos, Miriam; Moyà-Solà, Salvador; Alba, David M. (2012-09-01). "The nasal and paranasal architecture of the Middle Miocene ape Pierolapithecus catalaunicus (primates: Hominidae): Phylogenetic implications". Journal of Human Evolution. 63 (3): 497–506. Bibcode:2012JHumE..63..497P. doi:10.1016/j.jhevol.2012.05.012. ISSN 0047-2484. PMID 22819226.
- ^ a b Sevim-Erol, Ayla; Begun, D. R.; Sözer, Ç Sönmez; Mayda, S.; van den Hoek Ostende, L. W.; Martin, R. M. G.; Alçiçek, M. Cihat (2023-08-23). "A new ape from Türkiye and the radiation of late Miocene hominines". Communications Biology. 6 (1): 842. doi:10.1038/s42003-023-05210-5. ISSN 2399-3642. PMC 10447513. PMID 37612372.
- ^ Johnson, Mark (24 October 2023). "Scientists reconstructed the face of a 12 million-year-old great ape - Fossils of the extinct species Pierolapithecus catalaunicus may reveal clues about our origins". The Washington Post. Archived from the original on 24 October 2023. Retrieved 25 October 2023.
- ^ Pugh, Kelsey D.; et al. (16 October 2023). "The reconstructed cranium of Pierolapithecus and the evolution of the great ape face". PNAS. 120 (44): e2218778120. Bibcode:2023PNAS..12018778P. doi:10.1073/pnas.2218778120. PMC 10622906. PMID 37844214.
- ^ a b c Casanovasvilar, I; Alba, D; Moyasola, S; Galindo, J; Cabrera, L; Garces, M; Furio, M; Robles, J; Kohler, M; Angelone, C (2008). "Biochronological, taphonomical, and paleoenvironmental background of the fossil great ape Pierolapithecus catalaunicus (Primates, Hominidae)". Journal of Human Evolution. 55 (4): 589–603. Bibcode:2008JHumE..55..589C. doi:10.1016/j.jhevol.2008.05.004. PMID 18691737.
- ^ a b c Bezanson, Michele; MacKinnon, Katherine C; Riley, Erin; Campbell, Christina J; Nekaris, K.A.I (Anna); Estrada, Alejandro; Di Fiore, Anthony F; Ross, Stephen; Jones-Engel, Lisa E, eds. (2016-06-14). The International Encyclopedia of Primatology (1 ed.). Wiley. doi:10.1002/9781119179313.wbprim0216. ISBN 978-0-470-67337-9.
- ^ a b c d e Moya-Sola, S.; Köhler, M.; Alba, D. M.; Casanovas-Vilar, I.; Galindo, J. (2004). "Pierolapithecus catalaunicus, a New Middle Miocene Great Ape from Spain" (PDF). Science. 306 (5700): 1339–1344. Bibcode:2004Sci...306.1339M. doi:10.1126/science.1103094. PMID 15550663. S2CID 129576842.
- ^ a b Almécija, Sergio; Alba, David M.; Moyà-Solà, Salvador (2009). "Pierolapithecus and the functional morphology of Miocene ape hand phalanges: paleobiological and evolutionary implications". Journal of Human Evolution. 57 (3): 284–297. Bibcode:2009JHumE..57..284A. doi:10.1016/j.jhevol.2009.02.008. PMID 19631964.
- ^ Alba, David M.; Almécija, Sergio; Moyà-Solà, Salvador (2010-07-01). "Locomotor inferences in Pierolapithecus and Hispanopithecus: Reply to Deane and Begun (2008)". Journal of Human Evolution. 59 (1): 143–149. Bibcode:2010JHumE..59..143A. doi:10.1016/j.jhevol.2010.02.002. ISSN 0047-2484. PMID 20510436.
- ^ Pina, Marta; Almécija, Sergio; Alba, David M.; O'Neill, Matthew C.; Moyà-Solà, Salvador (2014). "The Middle Miocene Ape Pierolapithecus catalaunicus Exhibits Extant Great Ape-Like Morphometric Affinities on Its Patella: Inferences on Knee Function and Evolution". PLOS ONE. 9 (3): e91944. Bibcode:2014PLoSO...991944P. doi:10.1371/journal.pone.0091944. ISSN 1932-6203. PMC 3956854. PMID 24637777.
- ^ Hammond, Ashley S.; Alba, David M.; Almécija, Sergio; Moyà-Solà, Salvador (2013). "Middle Miocene Pierolapithecus provides a first glimpse into early hominid pelvic morphology". Journal of Human Evolution. 64 (6): 658–666. Bibcode:2013JHumE..64..658H. doi:10.1016/j.jhevol.2013.03.002. PMID 23545221.
- ^ a b Begun, D. R. (2015). Fossil record of Miocene hominoids (2nd ed.). Berlin: Springer. pp. 1304–1306. ISBN 978-3-642-39980-0.
- ^ a b c Alba, D. M.; Fortuny, J.; Moyà-Solà, S. (2010). "Enamel thickness in the Middle Miocene great apes Anoiapithecus , Pierolapithecus and Dryopithecus". Proceedings of the Royal Society B: Biological Sciences. 277 (1691): 2237–2245. doi:10.1098/rspb.2010.0218. ISSN 0962-8452. PMC 2880156. PMID 20335211.
- ^ Pugh, K. D.; Catalano, S. A.; Pérez de los Ríos, M.; Fortuny, J.; Shearer, B. M.; Vecino Gazabón, A.; Hammond, A. S.; Moyà-Solà, S.; Alba, D. M.; Almécija, S. (2023). "The reconstructed cranium of Pierolapithecus and the evolution of the great ape face". Proceedings of the National Academy of Sciences of the United States of America. 120 (44). e2218778120. Bibcode:2023PNAS..12018778P. doi:10.1073/pnas.2218778120. PMC 10622906. PMID 37844214.
- ^ Hammond, AS; Alba, DM; Almécija, S; Moyà-Solà, S (2013). "Middle Miocene hominid Pierolapithecus provides insight into early hominid pelvic morphology". Paleoanthropology. 2013 (2013): A16. ISSN 1545-0031.
- ^ Roegl, Fred (1999). "Mediterranean and Paratethys. Facts and hypotheses of an Oligocene to Miocene paleogeography (short overview)". Geol. Carpathica. 50: 339–349.
- ^ Nelson, Emma; Rolian, Campbell; Cashmore, Lisa; Shultz, Susanne (3 November 2010). "Digit ratios predict polygyny in early apes, Ardipithecus , Neanderthals and early modern humans but not in Australopithecus". Proceedings of the Royal Society B: Biological Sciences. 278 (1711): 1556–1563. doi:10.1098/rspb.2010.1740. ISSN 0962-8452. PMC 3081742. PMID 21047863. Retrieved 10 July 2024.