Biometric Evidence that Sexual Selection Has Shaped the Hominin Face
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{"title"=>"Biometric evidence that sexual selection has shaped the hominin face", "type"=>"journal", "authors"=>[{"first_name"=>"Eleanor M.", "last_name"=>"Weston", "scopus_author_id"=>"6701356382"}, {"first_name"=>"Adrian E.", "last_name"=>"Friday", "scopus_author_id"=>"7003555567"}, {"first_name"=>"Pietro", "last_name"=>"Liò", "scopus_author_id"=>"7004223170"}], "year"=>2007, "source"=>"PLoS ONE", "identifiers"=>{"sgr"=>"40249119910", "doi"=>"10.1371/journal.pone.0000710", "pui"=>"351330806", "pmid"=>"17684556", "scopus"=>"2-s2.0-40249119910", "issn"=>"19326203", "isbn"=>"1932-6203 (Electronic)\\r1932-6203 (Linking)"}, "id"=>"cb483124-f946-387c-b8dd-a1f77aa67087", "abstract"=>"We consider sex differences in human facial morphology in the context of developmental change. We show that at puberty, the height of the upper face, between the lip and the brow, develops differently in males and females, and that these differences are not explicable in terms of sex differences in body size. We find the same dimorphism in the faces of human ancestors. We propose that the relative shortening in men and lengthening in women of the anterior upper face at puberty is the mechanistic consequence of extreme maxillary rotation during ontogeny. A link between this developmental model and sexual dimorphism is made for the first time, and provides a new set of morphological criteria to sex human crania. This finding has important implications for the role of sexual selection in the evolution of anthropoid faces and for theories of human facial attractiveness.", "link"=>"http://www.mendeley.com/research/biometric-evidence-sexual-selection-shaped-hominin-face", "reader_count"=>174, "reader_count_by_academic_status"=>{"Unspecified"=>8, "Professor > Associate Professor"=>19, "Librarian"=>2, "Student > Doctoral Student"=>5, "Researcher"=>23, "Student > Ph. D. Student"=>37, "Student > Postgraduate"=>7, "Other"=>5, "Student > Master"=>22, "Student > Bachelor"=>24, "Lecturer"=>5, "Lecturer > Senior Lecturer"=>5, "Professor"=>12}, "reader_count_by_user_role"=>{"Unspecified"=>8, "Professor > Associate Professor"=>19, "Librarian"=>2, "Student > Doctoral Student"=>5, "Researcher"=>23, "Student > Ph. D. Student"=>37, "Student > Postgraduate"=>7, "Other"=>5, "Student > Master"=>22, "Student > Bachelor"=>24, "Lecturer"=>5, "Lecturer > Senior Lecturer"=>5, "Professor"=>12}, "reader_count_by_subject_area"=>{"Unspecified"=>12, "Agricultural and Biological Sciences"=>44, "Arts and Humanities"=>6, "Business, Management and Accounting"=>7, "Chemistry"=>1, "Computer Science"=>3, "Earth and Planetary Sciences"=>2, "Economics, Econometrics and Finance"=>3, "Engineering"=>1, "Biochemistry, Genetics and Molecular Biology"=>3, "Nursing and Health Professions"=>1, "Medicine and Dentistry"=>7, "Sports and Recreations"=>1, "Psychology"=>60, "Social Sciences"=>20, "Immunology and Microbiology"=>1, "Linguistics"=>2}, "reader_count_by_subdiscipline"=>{"Medicine and Dentistry"=>{"Medicine and Dentistry"=>7}, "Social Sciences"=>{"Social Sciences"=>20}, "Sports and Recreations"=>{"Sports and Recreations"=>1}, "Psychology"=>{"Psychology"=>60}, "Unspecified"=>{"Unspecified"=>12}, "Arts and Humanities"=>{"Arts and Humanities"=>6}, "Engineering"=>{"Engineering"=>1}, "Chemistry"=>{"Chemistry"=>1}, "Earth and Planetary Sciences"=>{"Earth and Planetary Sciences"=>2}, "Economics, Econometrics and Finance"=>{"Economics, Econometrics and Finance"=>3}, "Immunology and Microbiology"=>{"Immunology and Microbiology"=>1}, "Agricultural and Biological Sciences"=>{"Agricultural and Biological Sciences"=>44}, "Computer Science"=>{"Computer Science"=>3}, "Business, Management and Accounting"=>{"Business, Management and Accounting"=>7}, "Nursing and Health Professions"=>{"Nursing and Health Professions"=>1}, "Linguistics"=>{"Linguistics"=>2}, "Biochemistry, Genetics and Molecular Biology"=>{"Biochemistry, Genetics and Molecular Biology"=>3}}, "reader_count_by_country"=>{"United States"=>1, "Japan"=>3, "Egypt"=>1, "United Kingdom"=>7, "Portugal"=>1, "Czech Republic"=>2, "Turkey"=>1, "Norway"=>1, "Luxembourg"=>1, "Brazil"=>2, "Poland"=>2, "Mexico"=>1, "South Africa"=>1, "Italy"=>1, "France"=>2, "Germany"=>1}, "group_count"=>5}

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Figshare

  • {"files"=>["https://ndownloader.figshare.com/files/946732"], "description"=>"<p>We show that adult males have relatively shorter upper faces for their breadth compared to females (<a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone-0000710-t001\" target=\"_blank\">Table 1</a>,<a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone-0000710-t002\" target=\"_blank\">2</a>, <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone-0000710-g001\" target=\"_blank\">Figure 1</a> and <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710.s002\" target=\"_blank\">Figures S2</a> and <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710.s003\" target=\"_blank\">S3</a>). Lines superimposed on the pictures illustrate this facial dimorphism: vertical lines are positioned against the left and right zygion, and horizontal lines are positioned against the nasion and prosthion of the male face. In comparison to the female face, the male face is wider (represented by the distance between left and right point zygion) and the upper facial height (represented by the distance between point nasion and point prosthion) is approximately the same. The photographs are presented as taken, with identical camera-to-subject distance, and without rescaling, in order to represent the actual size of the faces.</p>", "links"=>[], "tags"=>["craniofacial", "variables", "facial"], "article_id"=>617090, "categories"=>["Evolutionary Biology", "Ecology", "Developmental Biology", "Infectious Diseases"], "users"=>["Eleanor M. Weston", "Adrian E. Friday", "Pietro Liò"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000710.g002", "stats"=>{"downloads"=>5, "page_views"=>13, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Skeletal_craniofacial_variables_relate_to_facial_appearance_/617090", "title"=>"Skeletal craniofacial variables relate to facial appearance.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2007-08-08 01:58:10"}
  • {"files"=>["https://ndownloader.figshare.com/files/466351", "https://ndownloader.figshare.com/files/466389", "https://ndownloader.figshare.com/files/466459", "https://ndownloader.figshare.com/files/466523", "https://ndownloader.figshare.com/files/466661", "https://ndownloader.figshare.com/files/466705", "https://ndownloader.figshare.com/files/466848", "https://ndownloader.figshare.com/files/467008", "https://ndownloader.figshare.com/files/467192"], "description"=>"<div><p>We consider sex differences in human facial morphology in the context of developmental change. We show that at puberty, the height of the upper face, between the lip and the brow, develops differently in males and females, and that these differences are not explicable in terms of sex differences in body size. We find the same dimorphism in the faces of human ancestors. We propose that the relative shortening in men and lengthening in women of the anterior upper face at puberty is the mechanistic consequence of extreme maxillary rotation during ontogeny. A link between this developmental model and sexual dimorphism is made for the first time, and provides a new set of morphological criteria to sex human crania. This finding has important implications for the role of sexual selection in the evolution of anthropoid faces and for theories of human facial attractiveness.</p></div>", "links"=>[], "tags"=>["biometric", "shaped", "hominin"], "article_id"=>151923, "categories"=>["Evolutionary Biology", "Ecology", "Developmental Biology", "Cancer"], "users"=>["Eleanor M. Weston", "Adrian E. Friday", "Pietro Liò"], "doi"=>["https://dx.doi.org/10.1371/journal.pone.0000710.s001", "https://dx.doi.org/10.1371/journal.pone.0000710.s002", "https://dx.doi.org/10.1371/journal.pone.0000710.s003", "https://dx.doi.org/10.1371/journal.pone.0000710.s004", "https://dx.doi.org/10.1371/journal.pone.0000710.s005", "https://dx.doi.org/10.1371/journal.pone.0000710.s006", "https://dx.doi.org/10.1371/journal.pone.0000710.s007", "https://dx.doi.org/10.1371/journal.pone.0000710.s008", "https://dx.doi.org/10.1371/journal.pone.0000710.s009"], "stats"=>{"downloads"=>23, "page_views"=>46, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/Biometric_Evidence_that_Sexual_Selection_Has_Shaped_the_Hominin_Face/151923", "title"=>"Biometric Evidence that Sexual Selection Has Shaped the Hominin Face", "pos_in_sequence"=>0, "defined_type"=>4, "published_date"=>"2007-08-08 00:32:03"}
  • {"files"=>["https://ndownloader.figshare.com/files/947010"], "description"=>"<p>P values (<sup>*</sup><i>P</i>≤0.01; <sup>**</sup><i>P</i>≤0.001) from bootstrap tests comparing the major axis slope (above diagonal) and <i>y</i> intercepts (below diagonal) for male and female ontogenetic trajectories. Bold <i>P</i> values indicate level of significance after applying sequential Bonferroni correction. <i>R</i> values, major axis slope and <i>y</i> intercepts for trait relationships are given in <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710.s009\" target=\"_blank\">Table S3</a>. For trait definitions see below. In the mandible, the intercept and slope comparisons indicate that nearly all of the trait relationships comply with a model of ontogenetic scaling with the exception of the relationship between the distance between condyle and coronoid process of the mandible (C-CR) and CHT, CRHT, CBD, GBD, these differ between the sexes.</p><p>ML, length of mandible (gnathion [gn]–condylion laterale [cdl]); VL, ventral length of mandible (gn–gonion ventrale [go]); I-CR (infradentale [id]–coronion [cr]); CHT, posterior height of ramus (go–cdl); CRHT, height at coronoid process (go–cr); CBD, bi-condylar breadth (cdl–cdl), GBD, bi-gonial breadth (go–go); CRBD, bi-coronoidal breadth (cr–cr); SHT, symphysis height (gn–id); C-CR, distance between condyle and coronoid process (cdl–cr).</p>", "links"=>[], "tags"=>["comparisons", "ontogenetic"], "article_id"=>617365, "categories"=>["Evolutionary Biology", "Ecology", "Developmental Biology", "Infectious Diseases"], "users"=>["Eleanor M. Weston", "Adrian E. Friday", "Pietro Liò"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000710.t002", "stats"=>{"downloads"=>1, "page_views"=>7, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Results_from_comparisons_of_H_sapiens_male_and_female_ontogenetic_trajectories_/617365", "title"=>"Results from comparisons of <i>H. sapiens</i> male and female ontogenetic trajectories.", "pos_in_sequence"=>0, "defined_type"=>3, "published_date"=>"2007-08-08 02:02:45"}
  • {"files"=>["https://ndownloader.figshare.com/files/946986"], "description"=>"<p>P values (<sup>*</sup><i>P</i>≤0.01; <sup>**</sup><i>P</i>≤0.001) from bootstrap tests comparing the major axis slope (above diagonal) and <i>y</i> intercepts (below diagonal) for male and female ontogenetic trajectories. Bold <i>P</i> values indicate level of significance after applying sequential Bonferroni correction. <i>R</i> values, major axis slope and <i>y</i> intercepts for trait relationships are given in <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710.s009\" target=\"_blank\">Table S3</a>. For trait definitions see below and <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710.s001\" target=\"_blank\">Figure S1</a>. In the cranium the intercept comparisons indicate that most of the trait relationships (non-demarcated) comply to a model of ontogenetic scaling but some deviate from this model: the relationship between upper facial height (FHT) and BCL, BZW, BJW, BMW, FPZ, OW and the relationship between facial projection (FP) and BCL, BZW, BJW, BMW, FPZ, OW, differ between the sexes. The cranial slope comparisons are not found to be significantly different between the sexes with the exception of the relationship between facial projection (FP and FPZ) and BZW (but note slope comparisons not significant after Bonferroni correction, see equivalent intercept comparisons).</p><p>BCL, basicranial length (basion [ba]–nasion [n]); FL, upper facial length (ba–prosthion [pr]); FHT, upper facial height (n–pr); BZW, bizygomatic width (zygion [zy]–zy); BJW, bijugal width (jugale [ju]–ju); BMW, bimaxillary width (zygomaxillare [zm]–zm); FPZ, facial projection (pr–zy); FP, facial projection (pr–frontomalare temporale [fmt]); MW, bimastoid width (mastoideale [ms]–ms); OW, orbital width (frontomalare orbitale [fmo]–maxillofrontale [mf]).</p>", "links"=>[], "tags"=>["comparisons", "ontogenetic"], "article_id"=>617337, "categories"=>["Evolutionary Biology", "Ecology", "Developmental Biology", "Infectious Diseases"], "users"=>["Eleanor M. Weston", "Adrian E. Friday", "Pietro Liò"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000710.t001", "stats"=>{"downloads"=>6, "page_views"=>10, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Results_from_comparisons_of_H_sapiens_male_and_female_ontogenetic_trajectories_/617337", "title"=>"Results from comparisons of <i>H. sapiens</i> male and female ontogenetic trajectories.", "pos_in_sequence"=>0, "defined_type"=>3, "published_date"=>"2007-08-08 02:02:17"}
  • {"files"=>["https://ndownloader.figshare.com/files/946596"], "description"=>"<p>The relationship between bizygomatic width (BZW) and upper facial height (FHT) shows a departure from ontogenetic scaling. Major axis slopes and 95% confidence intervals: male 0.7847 (0.74–0.83), female 0.6988 (0.65–0. 75). The FHT value for specimen KNM-ER 406 is a conservative estimate as the subnasal region is slightly damaged <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710-Wood3\" target=\"_blank\">[28]</a>. However, a small increase in FHT would align this cranium even more closely to the male ontogenetic trajectory.</p>", "links"=>[], "tags"=>["ontogenetic", "trajectories", "plotted", "fossil", "hominin"], "article_id"=>616946, "categories"=>["Evolutionary Biology", "Ecology", "Developmental Biology", "Infectious Diseases"], "users"=>["Eleanor M. Weston", "Adrian E. Friday", "Pietro Liò"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000710.g001", "stats"=>{"downloads"=>5, "page_views"=>7, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_Male_and_female_H_sapiens_ontogenetic_trajectories_plotted_with_fossil_hominin_crania_/616946", "title"=>"Male and female <i>H. sapiens</i> ontogenetic trajectories plotted with fossil hominin crania.", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2007-08-08 01:55:46"}
  • {"files"=>["https://ndownloader.figshare.com/files/946923"], "description"=>"<p>For the chimpanzee, sexual size dimorphism is shown to be statistically significant in BZW in age classes 6 and 7 (A) and no significant sexual size dimorphism is evident in FHT for any age class (B). For the gorilla, sexual size dimorphism is evident in BZW (C) and FHT (D) for age classes 4, 5, and 7; BZW and FHT are sexually dimorphic in size as adults (age class 7). Age classes 1–7 plotted on the <i>x</i> axis; each class with females (F) plotted first and then males (M). Trait size on <i>y</i> axis (cm). The box plots indicate the median in white and the quantiles in colour. The dotted lines indicate the data range with outliers shown as isolated bars (for sample analysed see electronic Appendix in <a href=\"http://www.plosone.org/article/info:doi/10.1371/journal.pone.0000710#pone.0000710-Weston1\" target=\"_blank\">[17]</a>).</p>", "links"=>[], "tags"=>["skeletal", "dental"], "article_id"=>617277, "categories"=>["Evolutionary Biology", "Ecology", "Developmental Biology", "Infectious Diseases"], "users"=>["Eleanor M. Weston", "Adrian E. Friday", "Pietro Liò"], "doi"=>"https://dx.doi.org/10.1371/journal.pone.0000710.g003", "stats"=>{"downloads"=>11, "page_views"=>2, "likes"=>0}, "figshare_url"=>"https://figshare.com/articles/_A_comparison_of_male_and_female_skeletal_traits_versus_dental_category_age_class_for_Pan_troglodytes_and_Gorilla_gorilla_/617277", "title"=>"A comparison of male and female skeletal traits versus dental category (age class) for <i>Pan troglodytes</i> and <i>Gorilla gorilla.</i>", "pos_in_sequence"=>0, "defined_type"=>1, "published_date"=>"2007-08-08 02:01:17"}

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Relative Metric

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