Taxonomic and functional aspects of the patterning of enamel thickness distribution in extant large-bodied hominoids
One of the few uncontested viewpoints in studies of enamel thickness is that the molars of the African apes, Pan and Gorilla, possess “thin” enamel, while Pongo and modern humans possess varying degrees of “thick” enamel, even when interspecific differences in overall body or tooth size are taken in...
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description | One of the few uncontested viewpoints in studies of enamel thickness is that the molars of the African apes, Pan and Gorilla, possess “thin” enamel, while Pongo and modern humans possess varying degrees of “thick” enamel, even when interspecific differences in overall body or tooth size are taken into account. Such studies focus primarily on estimates of the total volume of enamel relative to tooth size (i.e., “relative” enamel thickness), as this is thought to bear directly on questions concerning dietary proclivities and phylogenetic relationships. Only recently have studies shifted focus to examining differences in the distribution of enamel across the tooth crown, i.e., the patterning of enamel thickness, as this may contribute to more refined models of tooth function and dietary adaptations in extant hominoids. Additionally, this feature has been suggested to be a reliable indicator of taxonomic affinity in early hominins, though no study has specifically addressed whether species‐specific patterns exist among known phena.
The aims of this paper were to test more explicitly whether enamel thickness patterning provides valuable taxonomic, functional, and/or phylogenetic information for maxillary molars of large‐bodied extant hominoids. A series of seven linear enamel thickness measurements was recorded in the plane of the mesial cusps in cross sections of a total of 62 maxillary molars of P. troglodytes, G. gorilla, P. pygmaeus, and H. sapiens to estimate the patterning of enamel thickness distribution. Results from a discriminant function analysis reveal that, overall, this trait reclassifies extant hominoid maxillary molars with 90% accuracy: 100% of extant Homo, 75.0% of Pongo, 83.3% of Pan, and 66.7% of Gorilla are reclassified correctly, indicating that this feature possesses a strong taxonomic signal. Furthermore, differences in the structure of the enamel cap are evident among hominoids: modern humans differ from Pongo in possessing proportionally thicker enamel in areas of the crown associated with shearing activity; Pan molars are better designed than those of Gorilla for generating a greater component of crushing/grinding loads. Thus, African ape molars are structurally dissimilar, even though they are both considered to belong to a morphologically homogeneous “thin‐enameled” group. Simple developmental mechanisms can be invoked to explain the sometimes subtle differences in the achievement of adult morphology. For instance, human and orangut |
doi_str_mv | 10.1002/(SICI)1096-8644(200002)111:2<221::AID-AJPA8>3.0.CO;2-G |
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The aims of this paper were to test more explicitly whether enamel thickness patterning provides valuable taxonomic, functional, and/or phylogenetic information for maxillary molars of large‐bodied extant hominoids. A series of seven linear enamel thickness measurements was recorded in the plane of the mesial cusps in cross sections of a total of 62 maxillary molars of P. troglodytes, G. gorilla, P. pygmaeus, and H. sapiens to estimate the patterning of enamel thickness distribution. Results from a discriminant function analysis reveal that, overall, this trait reclassifies extant hominoid maxillary molars with 90% accuracy: 100% of extant Homo, 75.0% of Pongo, 83.3% of Pan, and 66.7% of Gorilla are reclassified correctly, indicating that this feature possesses a strong taxonomic signal. Furthermore, differences in the structure of the enamel cap are evident among hominoids: modern humans differ from Pongo in possessing proportionally thicker enamel in areas of the crown associated with shearing activity; Pan molars are better designed than those of Gorilla for generating a greater component of crushing/grinding loads. Thus, African ape molars are structurally dissimilar, even though they are both considered to belong to a morphologically homogeneous “thin‐enameled” group. Simple developmental mechanisms can be invoked to explain the sometimes subtle differences in the achievement of adult morphology. For instance, human and orangutan molar cusps possess a similar degree of enamel thickness, but the possibility exists that despite similarities in morphology, each species follows a different sequence of secretory activity of enamel to achieve the final, albeit similar, degree of enamel thickness. Such a finding would suggest that the shared possession of “thick” or “thin” enamel among species may be phylogenetically uninformative, as it would not represent a developmental synapomorphy. Am J Phys Anthropol 111:221–244, 2000. © 2000 Wiley‐Liss, Inc.</description><identifier>ISSN: 0002-9483</identifier><identifier>EISSN: 1096-8644</identifier><identifier>DOI: 10.1002/(SICI)1096-8644(200002)111:2<221::AID-AJPA8>3.0.CO;2-G</identifier><identifier>PMID: 10640949</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Animals ; Anthropology, Physical ; Biological and medical sciences ; Biometry ; Classification ; Dental Enamel - anatomy & histology ; Diet ; enamel development ; enamel thickness ; Fundamental and applied biological sciences. Psychology ; great apes ; Hominidae ; Humans ; Mammalia ; mastication ; maxillary molars ; modern humans ; Molar - anatomy & histology ; Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus ; Phylogeny ; Primates ; Reference Values ; tooth function ; Vertebrates: digestive system ; Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution</subject><ispartof>American journal of physical anthropology, 2000-02, Vol.111 (2), p.221-244</ispartof><rights>Copyright © 2000 Wiley‐Liss, Inc.</rights><rights>2000 INIST-CNRS</rights><rights>Copyright 2000 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5278-5b7e4f34023d5ae5162c3b406a22fda9a4d3c1b0dffea1a166a5e03f151fc24c3</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%2F%28SICI%291096-8644%28200002%29111%3A2%3C221%3A%3AAID-AJPA8%3E3.0.CO%3B2-G$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291096-8644%28200002%29111%3A2%3C221%3A%3AAID-AJPA8%3E3.0.CO%3B2-G$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27846,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1392487$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10640949$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwartz, Gary T.</creatorcontrib><title>Taxonomic and functional aspects of the patterning of enamel thickness distribution in extant large-bodied hominoids</title><title>American journal of physical anthropology</title><addtitle>Am. J. Phys. Anthropol</addtitle><description>One of the few uncontested viewpoints in studies of enamel thickness is that the molars of the African apes, Pan and Gorilla, possess “thin” enamel, while Pongo and modern humans possess varying degrees of “thick” enamel, even when interspecific differences in overall body or tooth size are taken into account. Such studies focus primarily on estimates of the total volume of enamel relative to tooth size (i.e., “relative” enamel thickness), as this is thought to bear directly on questions concerning dietary proclivities and phylogenetic relationships. Only recently have studies shifted focus to examining differences in the distribution of enamel across the tooth crown, i.e., the patterning of enamel thickness, as this may contribute to more refined models of tooth function and dietary adaptations in extant hominoids. Additionally, this feature has been suggested to be a reliable indicator of taxonomic affinity in early hominins, though no study has specifically addressed whether species‐specific patterns exist among known phena.
The aims of this paper were to test more explicitly whether enamel thickness patterning provides valuable taxonomic, functional, and/or phylogenetic information for maxillary molars of large‐bodied extant hominoids. A series of seven linear enamel thickness measurements was recorded in the plane of the mesial cusps in cross sections of a total of 62 maxillary molars of P. troglodytes, G. gorilla, P. pygmaeus, and H. sapiens to estimate the patterning of enamel thickness distribution. Results from a discriminant function analysis reveal that, overall, this trait reclassifies extant hominoid maxillary molars with 90% accuracy: 100% of extant Homo, 75.0% of Pongo, 83.3% of Pan, and 66.7% of Gorilla are reclassified correctly, indicating that this feature possesses a strong taxonomic signal. Furthermore, differences in the structure of the enamel cap are evident among hominoids: modern humans differ from Pongo in possessing proportionally thicker enamel in areas of the crown associated with shearing activity; Pan molars are better designed than those of Gorilla for generating a greater component of crushing/grinding loads. Thus, African ape molars are structurally dissimilar, even though they are both considered to belong to a morphologically homogeneous “thin‐enameled” group. Simple developmental mechanisms can be invoked to explain the sometimes subtle differences in the achievement of adult morphology. For instance, human and orangutan molar cusps possess a similar degree of enamel thickness, but the possibility exists that despite similarities in morphology, each species follows a different sequence of secretory activity of enamel to achieve the final, albeit similar, degree of enamel thickness. Such a finding would suggest that the shared possession of “thick” or “thin” enamel among species may be phylogenetically uninformative, as it would not represent a developmental synapomorphy. Am J Phys Anthropol 111:221–244, 2000. © 2000 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Anthropology, Physical</subject><subject>Biological and medical sciences</subject><subject>Biometry</subject><subject>Classification</subject><subject>Dental Enamel - anatomy & histology</subject><subject>Diet</subject><subject>enamel development</subject><subject>enamel thickness</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>great apes</subject><subject>Hominidae</subject><subject>Humans</subject><subject>Mammalia</subject><subject>mastication</subject><subject>maxillary molars</subject><subject>modern humans</subject><subject>Molar - anatomy & histology</subject><subject>Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus</subject><subject>Phylogeny</subject><subject>Primates</subject><subject>Reference Values</subject><subject>tooth function</subject><subject>Vertebrates: digestive system</subject><subject>Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution</subject><issn>0002-9483</issn><issn>1096-8644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>K30</sourceid><recordid>eNqFkWtr1EAUhoModq3-BRlQpP2QdW65rVJYo667FFdotX47TCYz7bTZyTqT4PbfOzFLFRUcAkNOnvOeQ54oOiF4SjCmL4_OluXymOAijfOU8yOKw6HHhJAZfU0pmc3my7fxfPVpnp-wKZ6W61c0XtyLJnct96PJ0BIXPGcH0SPvr8NrGp6H0QHBKccFLyZRdy52rW03RiJha6R7KzvTWtEg4bdKdh61GnVXCm1F1ylnjb0cKsqKjWrCByNvrPIe1cZ3zlT90IyMRWrXCduhRrhLFVdtbVSNrsIY25raP44eaNF49WR_H0af3787Lz_Ep-vFspyfxjKhWR4nVaa4ZhxTVidCJSSlklUcp4JSXYtC8JpJUuFaayWIIGkqEoWZJgnRknLJDqMXY-7Wtd965TvYGC9V0wir2t5DhvMckyIN4LM_wOu2d-EveCA84zRwNAnUl5GSrvXeKQ1bZzbC3QLBMFgDGKzBoAAGBTBag2ANKARrAMEa_LQGDDCU61BfhOCn-_F9tVH1b7GjpgA83wPCS9FoJ6w0_hfHCsrzLGAXI_bdNOr2r-3-t9y_dhsLITkek4NmtbtLFu4G0oxlCVx8XEB5tirKxeoNfGU_AN7Bz9U</recordid><startdate>200002</startdate><enddate>200002</enddate><creator>Schwartz, Gary T.</creator><general>John Wiley & Sons, Inc</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>FIXVA</scope><scope>FKUCP</scope><scope>IBDFT</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope><scope>7X8</scope></search><sort><creationdate>200002</creationdate><title>Taxonomic and functional aspects of the patterning of enamel thickness distribution in extant large-bodied hominoids</title><author>Schwartz, Gary T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5278-5b7e4f34023d5ae5162c3b406a22fda9a4d3c1b0dffea1a166a5e03f151fc24c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Anthropology, Physical</topic><topic>Biological and medical sciences</topic><topic>Biometry</topic><topic>Classification</topic><topic>Dental Enamel - anatomy & histology</topic><topic>Diet</topic><topic>enamel development</topic><topic>enamel thickness</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>great apes</topic><topic>Hominidae</topic><topic>Humans</topic><topic>Mammalia</topic><topic>mastication</topic><topic>maxillary molars</topic><topic>modern humans</topic><topic>Molar - anatomy & histology</topic><topic>Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus</topic><topic>Phylogeny</topic><topic>Primates</topic><topic>Reference Values</topic><topic>tooth function</topic><topic>Vertebrates: digestive system</topic><topic>Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwartz, Gary T.</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>Periodicals Index Online Segment 03</collection><collection>Periodicals Index Online Segment 04</collection><collection>Periodicals Index Online Segment 27</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</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>Schwartz, Gary T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Taxonomic and functional aspects of the patterning of enamel thickness distribution in extant large-bodied hominoids</atitle><jtitle>American journal of physical anthropology</jtitle><addtitle>Am. J. Phys. Anthropol</addtitle><date>2000-02</date><risdate>2000</risdate><volume>111</volume><issue>2</issue><spage>221</spage><epage>244</epage><pages>221-244</pages><issn>0002-9483</issn><eissn>1096-8644</eissn><abstract>One of the few uncontested viewpoints in studies of enamel thickness is that the molars of the African apes, Pan and Gorilla, possess “thin” enamel, while Pongo and modern humans possess varying degrees of “thick” enamel, even when interspecific differences in overall body or tooth size are taken into account. Such studies focus primarily on estimates of the total volume of enamel relative to tooth size (i.e., “relative” enamel thickness), as this is thought to bear directly on questions concerning dietary proclivities and phylogenetic relationships. Only recently have studies shifted focus to examining differences in the distribution of enamel across the tooth crown, i.e., the patterning of enamel thickness, as this may contribute to more refined models of tooth function and dietary adaptations in extant hominoids. Additionally, this feature has been suggested to be a reliable indicator of taxonomic affinity in early hominins, though no study has specifically addressed whether species‐specific patterns exist among known phena.
The aims of this paper were to test more explicitly whether enamel thickness patterning provides valuable taxonomic, functional, and/or phylogenetic information for maxillary molars of large‐bodied extant hominoids. A series of seven linear enamel thickness measurements was recorded in the plane of the mesial cusps in cross sections of a total of 62 maxillary molars of P. troglodytes, G. gorilla, P. pygmaeus, and H. sapiens to estimate the patterning of enamel thickness distribution. Results from a discriminant function analysis reveal that, overall, this trait reclassifies extant hominoid maxillary molars with 90% accuracy: 100% of extant Homo, 75.0% of Pongo, 83.3% of Pan, and 66.7% of Gorilla are reclassified correctly, indicating that this feature possesses a strong taxonomic signal. Furthermore, differences in the structure of the enamel cap are evident among hominoids: modern humans differ from Pongo in possessing proportionally thicker enamel in areas of the crown associated with shearing activity; Pan molars are better designed than those of Gorilla for generating a greater component of crushing/grinding loads. Thus, African ape molars are structurally dissimilar, even though they are both considered to belong to a morphologically homogeneous “thin‐enameled” group. Simple developmental mechanisms can be invoked to explain the sometimes subtle differences in the achievement of adult morphology. For instance, human and orangutan molar cusps possess a similar degree of enamel thickness, but the possibility exists that despite similarities in morphology, each species follows a different sequence of secretory activity of enamel to achieve the final, albeit similar, degree of enamel thickness. Such a finding would suggest that the shared possession of “thick” or “thin” enamel among species may be phylogenetically uninformative, as it would not represent a developmental synapomorphy. Am J Phys Anthropol 111:221–244, 2000. © 2000 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10640949</pmid><doi>10.1002/(SICI)1096-8644(200002)111:2<221::AID-AJPA8>3.0.CO;2-G</doi><tpages>24</tpages></addata></record> |
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subjects | Animals Anthropology, Physical Biological and medical sciences Biometry Classification Dental Enamel - anatomy & histology Diet enamel development enamel thickness Fundamental and applied biological sciences. Psychology great apes Hominidae Humans Mammalia mastication maxillary molars modern humans Molar - anatomy & histology Mouth. Exocrine and endocrine salivary glands. Teeth. Esophagus Phylogeny Primates Reference Values tooth function Vertebrates: digestive system Vertebrates: general zoology, morphology, phylogeny, systematics, cytogenetics, geographical distribution |
title | Taxonomic and functional aspects of the patterning of enamel thickness distribution in extant large-bodied hominoids |
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