Comparative morphometrics of the primate apical tuft
The relationship between the structure and function of the primate apical tuft is poorly understood. This study addresses several hypotheses about apical tuft morphology using a large modern primate comparative sample. Two indices of tuft size are employed: expansion and robusticity. First, comparis...
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description | The relationship between the structure and function of the primate apical tuft is poorly understood. This study addresses several hypotheses about apical tuft morphology using a large modern primate comparative sample. Two indices of tuft size are employed: expansion and robusticity. First, comparisons of relative apical tuft size were drawn among extant nonhuman primate groups in terms of locomotion and phylogenetic category. Both of these factors appear to play a role in apical tuft size among nonhuman primates. Suspensory primates and all platyrrhines had the smallest apical tufts, while terrestrial quadrupeds and all strepsirrhines (regardless of locomotor category) had the largest tufts. Similarly, hypotheses regarding the apical tufts of hominins, especially the large tufts of Neandertals were addressed using a comparison of modern warm‐ and cold‐adapted humans. The results showed that cold‐adapted populations possessed smaller apical tufts than did warm‐adapted groups. Therefore, the cold‐adaptation hypothesis for Neandertal distal phalangeal morphology is not supported. Also, early modern and Early Upper Paleolithic humans had apical tufts that were significantly less expanded and less robust than those of Neandertals. The hypothesis that a large apical tuft serves as support for an expanded digital pulp is supported by radiographic analysis of modern humans in that a significant correlation was discovered between the width of the apical tuft and the width of the pulp. The implications of these findings for hypotheses about the association of apical tuft size and tool making in the hominin fossil record are discussed. Am J Phys Anthropol, 2007. © 2007 Wiley‐Liss, Inc. |
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This study addresses several hypotheses about apical tuft morphology using a large modern primate comparative sample. Two indices of tuft size are employed: expansion and robusticity. First, comparisons of relative apical tuft size were drawn among extant nonhuman primate groups in terms of locomotion and phylogenetic category. Both of these factors appear to play a role in apical tuft size among nonhuman primates. Suspensory primates and all platyrrhines had the smallest apical tufts, while terrestrial quadrupeds and all strepsirrhines (regardless of locomotor category) had the largest tufts. Similarly, hypotheses regarding the apical tufts of hominins, especially the large tufts of Neandertals were addressed using a comparison of modern warm‐ and cold‐adapted humans. The results showed that cold‐adapted populations possessed smaller apical tufts than did warm‐adapted groups. Therefore, the cold‐adaptation hypothesis for Neandertal distal phalangeal morphology is not supported. Also, early modern and Early Upper Paleolithic humans had apical tufts that were significantly less expanded and less robust than those of Neandertals. The hypothesis that a large apical tuft serves as support for an expanded digital pulp is supported by radiographic analysis of modern humans in that a significant correlation was discovered between the width of the apical tuft and the width of the pulp. The implications of these findings for hypotheses about the association of apical tuft size and tool making in the hominin fossil record are discussed. Am J Phys Anthropol, 2007. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 0002-9483</identifier><identifier>EISSN: 1096-8644</identifier><identifier>DOI: 10.1002/ajpa.20687</identifier><identifier>PMID: 17657781</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject><![CDATA[Adaptation, Physiological - physiology ; Analysis of Variance ; Anatomy, Comparative ; Animals ; Anthropology, Physical ; Archanthropus and paleanthropus ; Catarrhini - anatomy & histology ; Catarrhini - genetics ; Catarrhini - physiology ; Comparative analysis ; distal phalanges ; Finger Phalanges - anatomy & histology ; Finger Phalanges - physiology ; Fingers - anatomy & histology ; Fingers - physiology ; Fossils ; Genetic Drift ; Hominidae - anatomy & histology ; Hominidae - genetics ; Hominidae - physiology ; Human paleontology ; Humans ; Locomotion ; Methodology and general studies ; Morphometrics ; Neandertal ; Neanderthals ; Neanthropus ; Phylogeny ; Physical anthropology ; Platyrrhini - anatomy & histology ; Platyrrhini - genetics ; Platyrrhini - physiology ; Prehistory and protohistory ; Primate behaviour ; Primates ; Primates - anatomy & histology ; Primates - genetics ; Primates - physiology ; Primatology ; Tarsiidae - anatomy & histology ; Tarsiidae - genetics ; Tarsiidae - physiology ; Temperature ; Toe Phalanges - anatomy & histology ; Toe Phalanges - physiology]]></subject><ispartof>American journal of physical anthropology, 2007-12, Vol.134 (4), p.449-459</ispartof><rights>Copyright © 2007 Wiley‐Liss, Inc.</rights><rights>2008 INIST-CNRS</rights><rights>(c) 2007 Wiley-Liss</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4927-19ce54262a7603792de5e6583ca722c507e189c5aa7a4a7728509b2b562ce1983</citedby><cites>FETCH-LOGICAL-c4927-19ce54262a7603792de5e6583ca722c507e189c5aa7a4a7728509b2b562ce1983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fajpa.20687$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fajpa.20687$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19282531$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17657781$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mittra, Erik S.</creatorcontrib><creatorcontrib>Smith, Heather F.</creatorcontrib><creatorcontrib>Lemelin, Pierre</creatorcontrib><creatorcontrib>Jungers, William L.</creatorcontrib><title>Comparative morphometrics of the primate apical tuft</title><title>American journal of physical anthropology</title><addtitle>Am. J. Phys. Anthropol</addtitle><description>The relationship between the structure and function of the primate apical tuft is poorly understood. This study addresses several hypotheses about apical tuft morphology using a large modern primate comparative sample. Two indices of tuft size are employed: expansion and robusticity. First, comparisons of relative apical tuft size were drawn among extant nonhuman primate groups in terms of locomotion and phylogenetic category. Both of these factors appear to play a role in apical tuft size among nonhuman primates. Suspensory primates and all platyrrhines had the smallest apical tufts, while terrestrial quadrupeds and all strepsirrhines (regardless of locomotor category) had the largest tufts. Similarly, hypotheses regarding the apical tufts of hominins, especially the large tufts of Neandertals were addressed using a comparison of modern warm‐ and cold‐adapted humans. The results showed that cold‐adapted populations possessed smaller apical tufts than did warm‐adapted groups. Therefore, the cold‐adaptation hypothesis for Neandertal distal phalangeal morphology is not supported. Also, early modern and Early Upper Paleolithic humans had apical tufts that were significantly less expanded and less robust than those of Neandertals. The hypothesis that a large apical tuft serves as support for an expanded digital pulp is supported by radiographic analysis of modern humans in that a significant correlation was discovered between the width of the apical tuft and the width of the pulp. The implications of these findings for hypotheses about the association of apical tuft size and tool making in the hominin fossil record are discussed. Am J Phys Anthropol, 2007. © 2007 Wiley‐Liss, Inc.</description><subject>Adaptation, Physiological - physiology</subject><subject>Analysis of Variance</subject><subject>Anatomy, Comparative</subject><subject>Animals</subject><subject>Anthropology, Physical</subject><subject>Archanthropus and paleanthropus</subject><subject>Catarrhini - anatomy & histology</subject><subject>Catarrhini - genetics</subject><subject>Catarrhini - physiology</subject><subject>Comparative analysis</subject><subject>distal phalanges</subject><subject>Finger Phalanges - anatomy & histology</subject><subject>Finger Phalanges - physiology</subject><subject>Fingers - anatomy & histology</subject><subject>Fingers - physiology</subject><subject>Fossils</subject><subject>Genetic Drift</subject><subject>Hominidae - anatomy & histology</subject><subject>Hominidae - genetics</subject><subject>Hominidae - physiology</subject><subject>Human paleontology</subject><subject>Humans</subject><subject>Locomotion</subject><subject>Methodology and general studies</subject><subject>Morphometrics</subject><subject>Neandertal</subject><subject>Neanderthals</subject><subject>Neanthropus</subject><subject>Phylogeny</subject><subject>Physical anthropology</subject><subject>Platyrrhini - anatomy & histology</subject><subject>Platyrrhini - genetics</subject><subject>Platyrrhini - physiology</subject><subject>Prehistory and protohistory</subject><subject>Primate behaviour</subject><subject>Primates</subject><subject>Primates - anatomy & histology</subject><subject>Primates - genetics</subject><subject>Primates - physiology</subject><subject>Primatology</subject><subject>Tarsiidae - anatomy & histology</subject><subject>Tarsiidae - genetics</subject><subject>Tarsiidae - physiology</subject><subject>Temperature</subject><subject>Toe Phalanges - anatomy & histology</subject><subject>Toe Phalanges - physiology</subject><issn>0002-9483</issn><issn>1096-8644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtPGzEURq0KVELopj8AzYYuKk3qx_i1TCOaFEWURatK3Vg3zh0xMMMM9gTIv8d5FHYgWbIsn-9efYeQz4yOGKX8G9x0MOJUGf2BDBi1KjeqKA7IgKbf3BZGHJHjGG_SU6XzkRwxraTWhg1IMWmbDgL01QNmTRu667bBPlQ-Zm2Z9deYdaFqoMcMuspDnfWrsj8hhyXUET_t7yH58-P892SWz39Nf07G89wXluucWY-y4IqDVlRoy5coUUkjPGjOvaQambFeAmgoQGtuJLULvpCKe2TWiCH5spvbhfZ-hbF3TRU91jXcYbuKTqWATL3fBYWyQkumEvh1B_rQxhiwdNt6Ye0YdRuZbiPTbWUm-HQ_dbVocPmK7u0l4GwPQExuygB3voqvnOWGS7Hh2I57rGpcv7HSjS-uxv-X57tMFXt8eslAuHVKpzLu7-XUzbQuBP03c9_FM5PjmM8</recordid><startdate>200712</startdate><enddate>200712</enddate><creator>Mittra, Erik S.</creator><creator>Smith, Heather F.</creator><creator>Lemelin, Pierre</creator><creator>Jungers, William L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8BJ</scope><scope>FQK</scope><scope>JBE</scope><scope>7X8</scope></search><sort><creationdate>200712</creationdate><title>Comparative morphometrics of the primate apical tuft</title><author>Mittra, Erik S. ; Smith, Heather F. ; Lemelin, Pierre ; Jungers, William L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4927-19ce54262a7603792de5e6583ca722c507e189c5aa7a4a7728509b2b562ce1983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adaptation, Physiological - physiology</topic><topic>Analysis of Variance</topic><topic>Anatomy, Comparative</topic><topic>Animals</topic><topic>Anthropology, Physical</topic><topic>Archanthropus and paleanthropus</topic><topic>Catarrhini - anatomy & histology</topic><topic>Catarrhini - genetics</topic><topic>Catarrhini - physiology</topic><topic>Comparative analysis</topic><topic>distal phalanges</topic><topic>Finger Phalanges - anatomy & histology</topic><topic>Finger Phalanges - physiology</topic><topic>Fingers - anatomy & histology</topic><topic>Fingers - physiology</topic><topic>Fossils</topic><topic>Genetic Drift</topic><topic>Hominidae - anatomy & histology</topic><topic>Hominidae - genetics</topic><topic>Hominidae - physiology</topic><topic>Human paleontology</topic><topic>Humans</topic><topic>Locomotion</topic><topic>Methodology and general studies</topic><topic>Morphometrics</topic><topic>Neandertal</topic><topic>Neanderthals</topic><topic>Neanthropus</topic><topic>Phylogeny</topic><topic>Physical anthropology</topic><topic>Platyrrhini - anatomy & histology</topic><topic>Platyrrhini - genetics</topic><topic>Platyrrhini - physiology</topic><topic>Prehistory and protohistory</topic><topic>Primate behaviour</topic><topic>Primates</topic><topic>Primates - anatomy & histology</topic><topic>Primates - genetics</topic><topic>Primates - physiology</topic><topic>Primatology</topic><topic>Tarsiidae - anatomy & histology</topic><topic>Tarsiidae - genetics</topic><topic>Tarsiidae - physiology</topic><topic>Temperature</topic><topic>Toe Phalanges - anatomy & histology</topic><topic>Toe Phalanges - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mittra, Erik S.</creatorcontrib><creatorcontrib>Smith, Heather F.</creatorcontrib><creatorcontrib>Lemelin, Pierre</creatorcontrib><creatorcontrib>Jungers, William L.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>International Bibliography of the Social Sciences (IBSS)</collection><collection>International Bibliography of the Social Sciences</collection><collection>International Bibliography of the Social Sciences</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physical anthropology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mittra, Erik S.</au><au>Smith, Heather F.</au><au>Lemelin, Pierre</au><au>Jungers, William L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative morphometrics of the primate apical tuft</atitle><jtitle>American journal of physical anthropology</jtitle><addtitle>Am. J. Phys. Anthropol</addtitle><date>2007-12</date><risdate>2007</risdate><volume>134</volume><issue>4</issue><spage>449</spage><epage>459</epage><pages>449-459</pages><issn>0002-9483</issn><eissn>1096-8644</eissn><abstract>The relationship between the structure and function of the primate apical tuft is poorly understood. This study addresses several hypotheses about apical tuft morphology using a large modern primate comparative sample. Two indices of tuft size are employed: expansion and robusticity. First, comparisons of relative apical tuft size were drawn among extant nonhuman primate groups in terms of locomotion and phylogenetic category. Both of these factors appear to play a role in apical tuft size among nonhuman primates. Suspensory primates and all platyrrhines had the smallest apical tufts, while terrestrial quadrupeds and all strepsirrhines (regardless of locomotor category) had the largest tufts. Similarly, hypotheses regarding the apical tufts of hominins, especially the large tufts of Neandertals were addressed using a comparison of modern warm‐ and cold‐adapted humans. The results showed that cold‐adapted populations possessed smaller apical tufts than did warm‐adapted groups. Therefore, the cold‐adaptation hypothesis for Neandertal distal phalangeal morphology is not supported. Also, early modern and Early Upper Paleolithic humans had apical tufts that were significantly less expanded and less robust than those of Neandertals. The hypothesis that a large apical tuft serves as support for an expanded digital pulp is supported by radiographic analysis of modern humans in that a significant correlation was discovered between the width of the apical tuft and the width of the pulp. The implications of these findings for hypotheses about the association of apical tuft size and tool making in the hominin fossil record are discussed. Am J Phys Anthropol, 2007. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17657781</pmid><doi>10.1002/ajpa.20687</doi><tpages>11</tpages></addata></record> |
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subjects | Adaptation, Physiological - physiology Analysis of Variance Anatomy, Comparative Animals Anthropology, Physical Archanthropus and paleanthropus Catarrhini - anatomy & histology Catarrhini - genetics Catarrhini - physiology Comparative analysis distal phalanges Finger Phalanges - anatomy & histology Finger Phalanges - physiology Fingers - anatomy & histology Fingers - physiology Fossils Genetic Drift Hominidae - anatomy & histology Hominidae - genetics Hominidae - physiology Human paleontology Humans Locomotion Methodology and general studies Morphometrics Neandertal Neanderthals Neanthropus Phylogeny Physical anthropology Platyrrhini - anatomy & histology Platyrrhini - genetics Platyrrhini - physiology Prehistory and protohistory Primate behaviour Primates Primates - anatomy & histology Primates - genetics Primates - physiology Primatology Tarsiidae - anatomy & histology Tarsiidae - genetics Tarsiidae - physiology Temperature Toe Phalanges - anatomy & histology Toe Phalanges - physiology |
title | Comparative morphometrics of the primate apical tuft |
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