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            type="text/xsl"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1002/(ISSN)1096-8644" xmlns="http://purl.org/rss/1.0/"><title>American Journal of Physical Anthropology</title><description> Wiley Online Library : American Journal of Physical Anthropology</description><link>http://dx.doi.org/10.1002%2F%28ISSN%291096-8644</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">Copyright © 2012 Wiley Periodicals Inc.</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">0002-9483</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1096-8644</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">March 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">147</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">3</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">341</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">509</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1002/ajpa.v147.3/asset/cover.gif?v=1&amp;s=8841355817626365492384e5b3f0b3bd2b16742b"/><items><rdf:Seq><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22028"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22007"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22006"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22029"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22031"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22026"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22025"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22023"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22020"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22017"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22016"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22005"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.21649"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.21651"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.21653"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22000"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22001"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22002"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22008"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22009"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22010"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22011"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22013"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22015"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22024"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.21657"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22021"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22022"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22018"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22012"/><rdf:li rdf:resource="http://dx.doi.org/10.1002%2Fajpa.22004"/></rdf:Seq></items></channel><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22028" xmlns="http://purl.org/rss/1.0/"><title>Genetic variations and physical activity as determinants of limb bone morphology: An experimental approach using a mouse model</title><link>http://dx.doi.org/10.1002%2Fajpa.22028</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic variations and physical activity as determinants of limb bone morphology: An experimental approach using a mouse model</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ian J. Wallace</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Steven M. Tommasini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stefan Judex</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Theodore Garland</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Brigitte Demes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T06:38:19.026897-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22028</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22028</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22028</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>To gain insight into past human physical activity, anthropologists often infer functional loading history from the morphology of limb bone remains. It is assumed that, during life, loading had a positive, dose-dependent effect on bone structure that can be identified despite other effects. Here, we investigate the effects of genetic background and functional loading on limb bones using mice from an artificial selection experiment for high levels of voluntary wheel running. Growing males from four replicate high runner (HR) lines and four replicate nonselected control (C) lines were either allowed or denied wheel access for 2 months. Using μCT, femoral morphology was assessed at two cortical sites (mid-diaphysis, distal metaphysis) and one trabecular site (distal metaphysis). We found that genetic differences between the linetypes (HR vs. C), between the replicate lines within linetype, and between individuals with and without the so-called “mini-muscle” phenotype (caused by a Mendelian recessive gene that halves limb muscle mass) gave rise to significant variation in nearly all morphological indices examined. Wheel access also influenced femoral morphology, although the functional response did not generally result in enhanced structure. Exercise caused moderate periosteal enlargement, but relatively greater endocortical expansion, resulting in significantly thinner cortices and reduced bone area in the metaphysis. The magnitude of the response was independent of distance run. Mid-diaphyseal bone area and area moments, and trabecular morphology, were unaffected by exercise. These results underscore the strong influence of genetics on bone structure and the complexity by which mechanical stimuli may cause alterations in it. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>To gain insight into past human physical activity, anthropologists often infer functional loading history from the morphology of limb bone remains. It is assumed that, during life, loading had a positive, dose-dependent effect on bone structure that can be identified despite other effects. Here, we investigate the effects of genetic background and functional loading on limb bones using mice from an artificial selection experiment for high levels of voluntary wheel running. Growing males from four replicate high runner (HR) lines and four replicate nonselected control (C) lines were either allowed or denied wheel access for 2 months. Using μCT, femoral morphology was assessed at two cortical sites (mid-diaphysis, distal metaphysis) and one trabecular site (distal metaphysis). We found that genetic differences between the linetypes (HR vs. C), between the replicate lines within linetype, and between individuals with and without the so-called “mini-muscle” phenotype (caused by a Mendelian recessive gene that halves limb muscle mass) gave rise to significant variation in nearly all morphological indices examined. Wheel access also influenced femoral morphology, although the functional response did not generally result in enhanced structure. Exercise caused moderate periosteal enlargement, but relatively greater endocortical expansion, resulting in significantly thinner cortices and reduced bone area in the metaphysis. The magnitude of the response was independent of distance run. Mid-diaphyseal bone area and area moments, and trabecular morphology, were unaffected by exercise. These results underscore the strong influence of genetics on bone structure and the complexity by which mechanical stimuli may cause alterations in it. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22007" xmlns="http://purl.org/rss/1.0/"><title>Dental microwear texture and anthropoid diets</title><link>http://dx.doi.org/10.1002%2Fajpa.22007</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Dental microwear texture and anthropoid diets</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robert S. Scott</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mark F. Teaford</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter S. Ungar</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T06:37:58.805117-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22007</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22007</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22007</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Dental microwear has long been used as evidence concerning the diets of extinct species. Here, we present a comparative baseline series of dental microwear textures for a sample of 21 anthropoid primate species displaying interspecific and intraspecific dietary variability. Four dental microwear texture variables (complexity, anisotropy, textural fill volume, and heterogeneity) were computed based on scale-sensitive fractal analysis and high-resolution three-dimensional renderings of microwear surfaces collected using a white-light confocal profiler. The purpose of this analysis was to assess the extent to which these variables reflect variation in diet. Significant contrasts between species with diets known to include foods with differing material properties are clearly evident for all four microwear texture variables. In particular, species that consume more tough foods, such as leaves, tended to have high levels of anisotropy and low texture complexity. The converse was true for species including hard and brittle items in their diets either as staples or as fallback foods. These results reaffirm the utility of dental microwear texture analysis as an important tool in making dietary inferences based on fossil primate samples. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Dental microwear has long been used as evidence concerning the diets of extinct species. Here, we present a comparative baseline series of dental microwear textures for a sample of 21 anthropoid primate species displaying interspecific and intraspecific dietary variability. Four dental microwear texture variables (complexity, anisotropy, textural fill volume, and heterogeneity) were computed based on scale-sensitive fractal analysis and high-resolution three-dimensional renderings of microwear surfaces collected using a white-light confocal profiler. The purpose of this analysis was to assess the extent to which these variables reflect variation in diet. Significant contrasts between species with diets known to include foods with differing material properties are clearly evident for all four microwear texture variables. In particular, species that consume more tough foods, such as leaves, tended to have high levels of anisotropy and low texture complexity. The converse was true for species including hard and brittle items in their diets either as staples or as fallback foods. These results reaffirm the utility of dental microwear texture analysis as an important tool in making dietary inferences based on fossil primate samples. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22006" xmlns="http://purl.org/rss/1.0/"><title>Book review</title><link>http://dx.doi.org/10.1002%2Fajpa.22006</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Book review</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jill Pruetz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T06:37:47.003418-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22006</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22006</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22006</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Book Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22029" xmlns="http://purl.org/rss/1.0/"><title>Incremental enamel development in modern human deciduous anterior teeth</title><link>http://dx.doi.org/10.1002%2Fajpa.22029</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Incremental enamel development in modern human deciduous anterior teeth</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Patrick Mahoney</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T05:51:39.57084-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22029</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22029</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22029</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study reconstructs incremental enamel development for a sample of modern human deciduous mandibular (<em>n</em> = 42) and maxillary (<em>n</em> = 42) anterior (incisors and canines) teeth. Results are compared between anterior teeth, and with previous research for deciduous molars (Mahoney: Am J Phys Anthropol 144 (<a href="#bib63" rel="references:#bib63">2011</a>) 204–214) to identify developmental differences along the tooth row. Two hypotheses are tested: Retzius line periodicity will remain constant in teeth from the same jaw and range from 6 to 12 days among individuals, as in human permanent teeth; daily enamel secretion rates (DSRs) will not vary between deciduous teeth, as in some human permanent tooth types. A further aim is to search for links between deciduous incremental enamel development and the previously reported eruptionsequence. Retzius line periodicity in anterior teeth ranged between 5 and 6 days, but did not differ between an incisor and molar of one individual. Intradian line periodicity was 12 h. Mean cuspal DSRs varied slightly between equivalent regions along the tooth row. Mandibular incisors initiated enamel formation first, had the fastest mean DSRs, the greatest prenatal formation time, and based upon prior studies are the first deciduous tooth to erupt. Relatively rapid development in mandibular incisors in advance of early eruption may explain some of the variation in DSRs along the tooth row that cannot be explained by birth. Links between DSRs, enamel initiation times, and the deciduous eruption sequence are proposed. Anterior crown formation times presented here can contribute toward human infant age-at-death estimates. Regression equations for reconstructing formation time in worn incisors are given. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>This study reconstructs incremental enamel development for a sample of modern human deciduous mandibular (n = 42) and maxillary (n = 42) anterior (incisors and canines) teeth. Results are compared between anterior teeth, and with previous research for deciduous molars (Mahoney: Am J Phys Anthropol 144 (2011) 204–214) to identify developmental differences along the tooth row. Two hypotheses are tested: Retzius line periodicity will remain constant in teeth from the same jaw and range from 6 to 12 days among individuals, as in human permanent teeth; daily enamel secretion rates (DSRs) will not vary between deciduous teeth, as in some human permanent tooth types. A further aim is to search for links between deciduous incremental enamel development and the previously reported eruptionsequence. Retzius line periodicity in anterior teeth ranged between 5 and 6 days, but did not differ between an incisor and molar of one individual. Intradian line periodicity was 12 h. Mean cuspal DSRs varied slightly between equivalent regions along the tooth row. Mandibular incisors initiated enamel formation first, had the fastest mean DSRs, the greatest prenatal formation time, and based upon prior studies are the first deciduous tooth to erupt. Relatively rapid development in mandibular incisors in advance of early eruption may explain some of the variation in DSRs along the tooth row that cannot be explained by birth. Links between DSRs, enamel initiation times, and the deciduous eruption sequence are proposed. Anterior crown formation times presented here can contribute toward human infant age-at-death estimates. Regression equations for reconstructing formation time in worn incisors are given. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22031" xmlns="http://purl.org/rss/1.0/"><title>Fitness-related benefits of dominance in primates</title><link>http://dx.doi.org/10.1002%2Fajpa.22031</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fitness-related benefits of dominance in primates</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Majolo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Lehmann</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. de Bortoli Vizioli</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Schino</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T05:51:16.436068-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22031</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22031</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22031</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Dominance hierarchies are thought to provide various fitness-related benefits to dominant individuals (e.g., preferential access to food or mating partners). Remarkably, however, different studies on this topic have produced contradictory results, with some showing strong positive association between rank and fitness (i.e., dominants gain benefits over subordinates), others weak associations, and some others even revealing negative associations. Here, we investigate dominance-related benefits across primate species while controlling for phylogenetic effects. We extracted data from 94 published studies, representing 25 primate species (2 lemur species, 4 New World monkeys, 16 Old World monkeys, and 3 apes), to assess how dominance affects life-history and behavior. We used standard and phylogenetic meta-analyses to analyze the benefits of dominance in primates. Dominant females had higher infant survival to first year, although we found no significant effect of dominance on female feeding success. Results for female fecundity differed between the two meta-analytical approaches, with no effect of dominance on female fecundity after controlling for phylogeny. Dominant males had a higher fecundity and mating success than subordinate males. Finally, the benefits of dominance for female fecundity were stronger in species with a longer lifespan. Our study supports the view that dominance hierarchies are a key aspect of primate societies as they indeed provide a number of fitness-related benefits to individuals. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Dominance hierarchies are thought to provide various fitness-related benefits to dominant individuals (e.g., preferential access to food or mating partners). Remarkably, however, different studies on this topic have produced contradictory results, with some showing strong positive association between rank and fitness (i.e., dominants gain benefits over subordinates), others weak associations, and some others even revealing negative associations. Here, we investigate dominance-related benefits across primate species while controlling for phylogenetic effects. We extracted data from 94 published studies, representing 25 primate species (2 lemur species, 4 New World monkeys, 16 Old World monkeys, and 3 apes), to assess how dominance affects life-history and behavior. We used standard and phylogenetic meta-analyses to analyze the benefits of dominance in primates. Dominant females had higher infant survival to first year, although we found no significant effect of dominance on female feeding success. Results for female fecundity differed between the two meta-analytical approaches, with no effect of dominance on female fecundity after controlling for phylogeny. Dominant males had a higher fecundity and mating success than subordinate males. Finally, the benefits of dominance for female fecundity were stronger in species with a longer lifespan. Our study supports the view that dominance hierarchies are a key aspect of primate societies as they indeed provide a number of fitness-related benefits to individuals. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22026" xmlns="http://purl.org/rss/1.0/"><title>A new method to estimate adult age-at-death using the acetabulum</title><link>http://dx.doi.org/10.1002%2Fajpa.22026</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A new method to estimate adult age-at-death using the acetabulum</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stephanie E. Calce</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T05:50:58.188154-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22026</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22026</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22026</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Rissech et al. (J Forensic Sci 51 (<a href="#bib27" rel="references:#bib27">2006</a>) 213–229) described a method to estimate age-at-death of adult males using seven traits of the fused acetabulum. This study simplifies Rissech et al.'s technique and extends its application to adult females. Rissech et al.'s original scoring method was applied to a sample of 100 known-aged adults, three variables were selected based on stepwise multiple regression, and ages were collapsed into three broad ranges: young adult (17–39 years), middle adult (40–64 years), and old adult (65+ years). The revised method was applied to 249 new known-aged individuals from two other samples. To minimize observer bias, highlight the most critical traits, and encompass more age-related variation, unique digital renderings accompany morphological descriptions of age categories instead of photos. Three statistically significant characteristics highly correlated with age (<em>P</em> &lt; 0.05) are capable of estimating age-at-death with 81% accuracy, both sexes combined. For misidentified individuals the tendency was to underestimate age. Results of both intraobserver error testing and inter-rater reliability demonstrated a moderate to substantial agreement in scoring between observers. When estimating the degree of development of features osteophyte development of the acetabular rim was the most inconsistent between observers. The revised acetabular method shows promise in estimating age for adults, particularly for those over the age of 65 years. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Rissech et al. (J Forensic Sci 51 (2006) 213–229) described a method to estimate age-at-death of adult males using seven traits of the fused acetabulum. This study simplifies Rissech et al.'s technique and extends its application to adult females. Rissech et al.'s original scoring method was applied to a sample of 100 known-aged adults, three variables were selected based on stepwise multiple regression, and ages were collapsed into three broad ranges: young adult (17–39 years), middle adult (40–64 years), and old adult (65+ years). The revised method was applied to 249 new known-aged individuals from two other samples. To minimize observer bias, highlight the most critical traits, and encompass more age-related variation, unique digital renderings accompany morphological descriptions of age categories instead of photos. Three statistically significant characteristics highly correlated with age (P &lt; 0.05) are capable of estimating age-at-death with 81% accuracy, both sexes combined. For misidentified individuals the tendency was to underestimate age. Results of both intraobserver error testing and inter-rater reliability demonstrated a moderate to substantial agreement in scoring between observers. When estimating the degree of development of features osteophyte development of the acetabular rim was the most inconsistent between observers. The revised acetabular method shows promise in estimating age for adults, particularly for those over the age of 65 years. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22025" xmlns="http://purl.org/rss/1.0/"><title>Skeletal development in Pan paniscus with comparisons to Pan troglodytes</title><link>http://dx.doi.org/10.1002%2Fajpa.22025</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skeletal development in Pan paniscus with comparisons to Pan troglodytes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Debra R. Bolter</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adrienne L. Zihlman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T05:50:39.426911-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22025</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22025</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22025</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Fusion of skeletal elements provides markers for timing of growth and is one component of a chimpanzee's physical development. Epiphyseal closure defines bone growth and signals a mature skeleton. Most of what we know about timing of development in chimpanzees derives from dental studies on <em>Pan troglodytes</em>. Much less is known about the sister species, <em>Pan paniscus</em>, with few in captivity and a wild range restricted to central Africa. Here, we report on the timing of skeletal fusion for female captive <em>P. paniscus</em> (<em>n</em> = 5) whose known ages range from 0.83 to age 11.68 years. Observations on the skeletons were made after the individuals were dissected and bones cleaned. Comparisons with 10 female captive <em>P. troglodytes</em> confirm a generally uniform pattern in the sequence of skeletal fusion in the two captive species. We also compared the <em>P. paniscus</em> to a sample of three unknown-aged female wild <em>P. paniscus</em>, and 10 female wild <em>P. troglodytes</em> of known age from the Taï National Park, Côte d'Ivoire. The sequence of teeth emergence to bone fusion is generally consistent between the two species, with slight variations in late juvenile and subadult stages. The direct-age comparisons show that skeletal growth in captive <em>P. paniscus</em> is accelerated compared with both captive and wild <em>P. troglodytes</em> populations. The skeletal data combined with dental stages have implications for estimating the life stage of immature skeletal materials of wild <em>P. paniscus</em> and for more broadly comparing the skeletal growth rates among captive and wild chimpanzees (<em>Pan</em>), <em>Homo sapiens</em>, and fossil hominins. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Fusion of skeletal elements provides markers for timing of growth and is one component of a chimpanzee's physical development. Epiphyseal closure defines bone growth and signals a mature skeleton. Most of what we know about timing of development in chimpanzees derives from dental studies on Pan troglodytes. Much less is known about the sister species, Pan paniscus, with few in captivity and a wild range restricted to central Africa. Here, we report on the timing of skeletal fusion for female captive P. paniscus (n = 5) whose known ages range from 0.83 to age 11.68 years. Observations on the skeletons were made after the individuals were dissected and bones cleaned. Comparisons with 10 female captive P. troglodytes confirm a generally uniform pattern in the sequence of skeletal fusion in the two captive species. We also compared the P. paniscus to a sample of three unknown-aged female wild P. paniscus, and 10 female wild P. troglodytes of known age from the Taï National Park, Côte d'Ivoire. The sequence of teeth emergence to bone fusion is generally consistent between the two species, with slight variations in late juvenile and subadult stages. The direct-age comparisons show that skeletal growth in captive P. paniscus is accelerated compared with both captive and wild P. troglodytes populations. The skeletal data combined with dental stages have implications for estimating the life stage of immature skeletal materials of wild P. paniscus and for more broadly comparing the skeletal growth rates among captive and wild chimpanzees (Pan), Homo sapiens, and fossil hominins. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22023" xmlns="http://purl.org/rss/1.0/"><title>The relationship between musculoskeletal stress markers and biomechanical properties of the humeral diaphysis</title><link>http://dx.doi.org/10.1002%2Fajpa.22023</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The relationship between musculoskeletal stress markers and biomechanical properties of the humeral diaphysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sirpa Niinimäki</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-13T05:50:01.824838-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22023</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22023</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22023</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Musculoskeletal stress markers (MSM) at entheses and bone biomechanical properties are used in activity reconstructions. The effect of physical activity on bone biomechanical properties is well established but the relative role of physical activity on MSM is less well known. In this article, it is hypothesized that the same causal mechanisms should affect MSM development as those responsible for bone biomechanical properties. Further, there should be a correlation between MSMs and bone cross-sectional properties as both are considered to reflect physical activity. This was tested using three skeletal samples: early 20th century Finnish (Helsinki) and two medieval English (Blackgate and York) populations. Torsional/average bending rigidity (<em>J</em>) for four cross-sectional locations at 80, 65, 50, and 35% of humeral length from the distal end was calculated and pectoralis major, teres major, and deltoid were scored for MSM. Correlations between MSM and size-standardized <em>J</em> were significant for many comparisons, although they were stronger in males than in females, especially on the right side. In ANOVAs, sample was found to be a significant influence on the right side in both sexes. Using an aggregated MSM score, covariance between <em>J</em> and high MSM scores was again stronger in males. Covariance between <em>J</em> and MSM was found both at cross-sectional locations under muscle insertions and at more distant locations, demonstrating both direct and general effects of muscular loadings applied to diaphyses. Thus, the two types of skeletal markers appear to be related to similar underlying mechanical factors, but effects may also be sex- and sample-specific. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Musculoskeletal stress markers (MSM) at entheses and bone biomechanical properties are used in activity reconstructions. The effect of physical activity on bone biomechanical properties is well established but the relative role of physical activity on MSM is less well known. In this article, it is hypothesized that the same causal mechanisms should affect MSM development as those responsible for bone biomechanical properties. Further, there should be a correlation between MSMs and bone cross-sectional properties as both are considered to reflect physical activity. This was tested using three skeletal samples: early 20th century Finnish (Helsinki) and two medieval English (Blackgate and York) populations. Torsional/average bending rigidity (J) for four cross-sectional locations at 80, 65, 50, and 35% of humeral length from the distal end was calculated and pectoralis major, teres major, and deltoid were scored for MSM. Correlations between MSM and size-standardized J were significant for many comparisons, although they were stronger in males than in females, especially on the right side. In ANOVAs, sample was found to be a significant influence on the right side in both sexes. Using an aggregated MSM score, covariance between J and high MSM scores was again stronger in males. Covariance between J and MSM was found both at cross-sectional locations under muscle insertions and at more distant locations, demonstrating both direct and general effects of muscular loadings applied to diaphyses. Thus, the two types of skeletal markers appear to be related to similar underlying mechanical factors, but effects may also be sex- and sample-specific. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22020" xmlns="http://purl.org/rss/1.0/"><title>Early pleistocene human humeri from the gran dolina-TD6 site (sierra de atapuerca, spain)</title><link>http://dx.doi.org/10.1002%2Fajpa.22020</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Early pleistocene human humeri from the gran dolina-TD6 site (sierra de atapuerca, spain)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">José María Bermúdez de Castro</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">José Miguel Carretero</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rebeca García-González</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laura Rodríguez-García</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">María Martinón-Torres</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jordi Rosell</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ruth Blasco</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laura Martín-Francés</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mario Modesto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eudald Carbonell</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-10T09:33:12.087624-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22020</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22020</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22020</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this report, we present a morphometric comparative study of two Early Pleistocene humeri recovered from the TD6 level of the Gran Dolina cave site in Sierra de Atapuerca, northern Spain. ATD6-121 belongs to a child between 4 and 6 years old, whereas ATD6-148 corresponds to an adult. ATD6-148 exhibits the typical pattern of the genus <em>Homo,</em> but it also shows a large olecranon fossa and very thin medial and lateral pillars (also present in ATD6-121), sharing these features with European Middle Pleistocene hominins, Neandertals, and the Bodo Middle Pleistocene humerus. The morphology of the distal epiphysis, together with a few dental traits, suggests a phylogenetic relationship between the TD6 hominins and the Neandertal lineage. Given the older geochronological age of these hominins (ca. 900 ka), which is far from the age estimated by palaeogenetic studies for the population divergence of modern humans and Neandertals (ca. 400 ka), we suggest that this suite of derived “Neandertal” features appeared early in the evolution of the genus <em>Homo</em>. Thus, these features are not “Neandertal” apomorphies but traits which appeared in an ancestral and polymorphic population during the Early Pleistocene. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>In this report, we present a morphometric comparative study of two Early Pleistocene humeri recovered from the TD6 level of the Gran Dolina cave site in Sierra de Atapuerca, northern Spain. ATD6-121 belongs to a child between 4 and 6 years old, whereas ATD6-148 corresponds to an adult. ATD6-148 exhibits the typical pattern of the genus Homo, but it also shows a large olecranon fossa and very thin medial and lateral pillars (also present in ATD6-121), sharing these features with European Middle Pleistocene hominins, Neandertals, and the Bodo Middle Pleistocene humerus. The morphology of the distal epiphysis, together with a few dental traits, suggests a phylogenetic relationship between the TD6 hominins and the Neandertal lineage. Given the older geochronological age of these hominins (ca. 900 ka), which is far from the age estimated by palaeogenetic studies for the population divergence of modern humans and Neandertals (ca. 400 ka), we suggest that this suite of derived “Neandertal” features appeared early in the evolution of the genus Homo. Thus, these features are not “Neandertal” apomorphies but traits which appeared in an ancestral and polymorphic population during the Early Pleistocene. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22017" xmlns="http://purl.org/rss/1.0/"><title>Craniodental features in male Mandrillus may signal size and fitness: An allometric approach</title><link>http://dx.doi.org/10.1002%2Fajpa.22017</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Craniodental features in male Mandrillus may signal size and fitness: An allometric approach</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emily B. Klopp</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-10T09:32:01.450165-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22017</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22017</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22017</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>According to a hypothesis in the broader mammalian literature, secondary sexual characteristics that have evolved to signal fitness and size to other conspecifics should exhibit positive allometry across adult males within a species. Here this hypothesis is tested in the genus <em>Mandrillus</em>. The overbuilding of bony features in larger individuals necessitates a functional explanation as bone is metabolically expensive to produce and maintain. Canine size and size of the maxillary ridge are scaled against a body size surrogate in intraspecific samples of male <em>Mandrillus sphinx</em> (mandrills) and <em>Mandrillus leucophaeus</em> (drills). Areal dimensions are weighted more heavily as they represent the size of a feature as it is viewed by individuals. Measures of the maxillary ridge and canine tooth are significantly correlated with the size surrogate and scale with positive allometry in both samples supporting the hypothesis that these features function to advertise a male's body size and fitness to other males competing for mates and potential discerning females. This is the first study in primates to test for intraspecific positive allometric scaling of bony facial features in adult males based on a theory of fitness signaling and sexual selection. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>According to a hypothesis in the broader mammalian literature, secondary sexual characteristics that have evolved to signal fitness and size to other conspecifics should exhibit positive allometry across adult males within a species. Here this hypothesis is tested in the genus Mandrillus. The overbuilding of bony features in larger individuals necessitates a functional explanation as bone is metabolically expensive to produce and maintain. Canine size and size of the maxillary ridge are scaled against a body size surrogate in intraspecific samples of male Mandrillus sphinx (mandrills) and Mandrillus leucophaeus (drills). Areal dimensions are weighted more heavily as they represent the size of a feature as it is viewed by individuals. Measures of the maxillary ridge and canine tooth are significantly correlated with the size surrogate and scale with positive allometry in both samples supporting the hypothesis that these features function to advertise a male's body size and fitness to other males competing for mates and potential discerning females. This is the first study in primates to test for intraspecific positive allometric scaling of bony facial features in adult males based on a theory of fitness signaling and sexual selection. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22016" xmlns="http://purl.org/rss/1.0/"><title>Gait selection and the ontogeny of quadrupedal walking in squirrel monkeys (Saimiri boliviensis)</title><link>http://dx.doi.org/10.1002%2Fajpa.22016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gait selection and the ontogeny of quadrupedal walking in squirrel monkeys (Saimiri boliviensis)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jesse W. Young</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-10T09:31:21.628254-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22016</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22016</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Locomotor researchers have long known that adult primates employ a unique footfall sequence during walking. Most mammals use lateral sequence (LS) gaits, in which hind foot touchdowns are followed by ipsilateral forefoot touchdowns. In contrast, most quadrupedal primates use diagonal sequence (DS) gaits, in which hind foot touchdowns are followed by contralateral forefoot touchdowns. However, gait selection in immature primates is more variable, with infants and juveniles frequently using LS gaits either exclusively or in addition to DS gaits. I explored the developmental bases for this phenomenon by examining the ontogeny of gait selection in juvenile squirrel monkeys walking on flat and simulated arboreal substrates (i.e., a raised pole). Although DS gaits predominated throughout development, the juvenile squirrel monkeys nonetheless utilized LS gaits in one-third of the ground strides and in one-sixth of pole strides. Multiple logistic regression analyses showed that gait selection within the juvenile squirrel monkey sample was not significantly associated with either age or body mass per se, arguing against the oft-cited argument that general neuromuscular maturation is responsible for ontogenetic changes in preferred footfall sequence. Rather, lower level biomechanical variables, specifically the position of the whole-body center of mass and the potential for interference between ipsilateral fore and hindlimbs, best explained variation in footfall patterns. Overall, results demonstrate the promise of developmental studies of growth and locomotor development to serve as “natural laboratories” in which to explore how variability in morphology is, or is not, associated with variability in locomotor behavior. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Locomotor researchers have long known that adult primates employ a unique footfall sequence during walking. Most mammals use lateral sequence (LS) gaits, in which hind foot touchdowns are followed by ipsilateral forefoot touchdowns. In contrast, most quadrupedal primates use diagonal sequence (DS) gaits, in which hind foot touchdowns are followed by contralateral forefoot touchdowns. However, gait selection in immature primates is more variable, with infants and juveniles frequently using LS gaits either exclusively or in addition to DS gaits. I explored the developmental bases for this phenomenon by examining the ontogeny of gait selection in juvenile squirrel monkeys walking on flat and simulated arboreal substrates (i.e., a raised pole). Although DS gaits predominated throughout development, the juvenile squirrel monkeys nonetheless utilized LS gaits in one-third of the ground strides and in one-sixth of pole strides. Multiple logistic regression analyses showed that gait selection within the juvenile squirrel monkey sample was not significantly associated with either age or body mass per se, arguing against the oft-cited argument that general neuromuscular maturation is responsible for ontogenetic changes in preferred footfall sequence. Rather, lower level biomechanical variables, specifically the position of the whole-body center of mass and the potential for interference between ipsilateral fore and hindlimbs, best explained variation in footfall patterns. Overall, results demonstrate the promise of developmental studies of growth and locomotor development to serve as “natural laboratories” in which to explore how variability in morphology is, or is not, associated with variability in locomotor behavior. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22005" xmlns="http://purl.org/rss/1.0/"><title>Book review: Mammal Teeth: Origin, Evolution, and Diversity</title><link>http://dx.doi.org/10.1002%2Fajpa.22005</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Book review: Mammal Teeth: Origin, Evolution, and Diversity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter W. Lucas</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-20T04:18:17.119199-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22005</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22005</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22005</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Book Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.21649" xmlns="http://purl.org/rss/1.0/"><title>Russian ethnic history inferred from mitochondrial DNA diversity</title><link>http://dx.doi.org/10.1002%2Fajpa.21649</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Russian ethnic history inferred from mitochondrial DNA diversity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Irina Morozova</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alexey Evsyukov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrey Kon'kov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alexandra Grosheva</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Olga Zhukova</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sergey Rychkov</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.21649</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.21649</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.21649</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">341</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">351</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>With the aim of gaining insight into the genetic history of the Russians, we have studied mitochondrial DNA diversity among a number of modern Russian populations. Polymorphisms in mtDNA markers (HVS-I and restriction sites of the coding region) of populations from 14 regions within present-day European Russia were investigated. Based on analysis of the mitochondrial gene pool geographic structure, we have identified three different elements in it and a vast “intermediate” zone between them. The analysis of the genetic distances from these elements to the European ethnic groups revealed the main causes of the Russian mitochondrial gene pool differentiation. The investigation of this pattern in historic perspective showed that the structure of the mitochondrial gene pool of the present-day Russians largely conforms to the tribal structure of the medieval Slavs who laid the foundation of modern Russians. Our results indicate that the formation of the genetic diversity currently observed among Russians can be traced to the second half of the first millennium A.D., the time of the colonization of the East European Plain by the Slavic tribes. Patterns of diversity are explained by both the impact of the native population of the East European Plain and by genetic differences among the early Slavs. Am J Phys Anthropol , 2012. © 2011Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>With the aim of gaining insight into the genetic history of the Russians, we have studied mitochondrial DNA diversity among a number of modern Russian populations. Polymorphisms in mtDNA markers (HVS-I and restriction sites of the coding region) of populations from 14 regions within present-day European Russia were investigated. Based on analysis of the mitochondrial gene pool geographic structure, we have identified three different elements in it and a vast “intermediate” zone between them. The analysis of the genetic distances from these elements to the European ethnic groups revealed the main causes of the Russian mitochondrial gene pool differentiation. The investigation of this pattern in historic perspective showed that the structure of the mitochondrial gene pool of the present-day Russians largely conforms to the tribal structure of the medieval Slavs who laid the foundation of modern Russians. Our results indicate that the formation of the genetic diversity currently observed among Russians can be traced to the second half of the first millennium A.D., the time of the colonization of the East European Plain by the Slavic tribes. Patterns of diversity are explained by both the impact of the native population of the East European Plain and by genetic differences among the early Slavs. Am J Phys Anthropol , 2012. © 2011Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.21651" xmlns="http://purl.org/rss/1.0/"><title>Multivariate carbon and nitrogen stable isotope model for the reconstruction of prehistoric human diet</title><link>http://dx.doi.org/10.1002%2Fajpa.21651</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Multivariate carbon and nitrogen stable isotope model for the reconstruction of prehistoric human diet</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A.W. Froehle</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C.M. Kellner</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M.J. Schoeninger</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.21651</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.21651</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.21651</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">352</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">369</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Using a sample of published archaeological data, we expand on an earlier bivariate carbon model for diet reconstruction by adding bone collagen nitrogen stable isotope values (δ<sup>15</sup>N), which provide information on trophic level and consumption of terrestrial vs. marine protein. The bivariate carbon model (δ<sup>13</sup>C<sub>apatite</sub> vs. δ<sup>13</sup>C<sub>collagen</sub>) provides detailed information on the isotopic signatures of whole diet and dietary protein, but is limited in its ability to distinguish between C<sub>4</sub> and marine protein. Here, using cluster analysis and discriminant function analysis, we generate a multivariate diet reconstruction model that incorporates δ<sup>13</sup>C<sub>apatite</sub>, δ<sup>13</sup>C<sub>collagen</sub>, and δ<sup>15</sup>N holistically. Inclusion of the δ<sup>15</sup>N data proves useful in resolving protein-related limitations of the bivariate carbon model, and splits the sample into five distinct dietary clusters. Two significant discriminant functions account for 98.8% of the sample variance, providing a multivariate model for diet reconstruction. Both carbon variables dominate the first function, while δ<sup>15</sup>N most strongly influences the second. Independent support for the functions' ability to accurately classify individuals according to diet comes from a small sample of experimental rats, which cluster as expected from their diets. The new model also provides a statistical basis for distinguishing between food sources with similar isotopic signatures, as in a previously analyzed archaeological population from Saipan (see Ambrose et al.: AJPA 104(<a href="#bib5" rel="references:#bib5">1997</a>) 343-361). Our model suggests that the Saipan islanders' <sup>13</sup>C-enriched signal derives mainly from sugarcane, not seaweed. Further development and application of this model can similarly improve dietary reconstructions in archaeological, paleontological, and primatological contexts. Am J Phys Anthropol, 2012. © 2011 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Using a sample of published archaeological data, we expand on an earlier bivariate carbon model for diet reconstruction by adding bone collagen nitrogen stable isotope values (δ15N), which provide information on trophic level and consumption of terrestrial vs. marine protein. The bivariate carbon model (δ13Capatite vs. δ13Ccollagen) provides detailed information on the isotopic signatures of whole diet and dietary protein, but is limited in its ability to distinguish between C4 and marine protein. Here, using cluster analysis and discriminant function analysis, we generate a multivariate diet reconstruction model that incorporates δ13Capatite, δ13Ccollagen, and δ15N holistically. Inclusion of the δ15N data proves useful in resolving protein-related limitations of the bivariate carbon model, and splits the sample into five distinct dietary clusters. Two significant discriminant functions account for 98.8% of the sample variance, providing a multivariate model for diet reconstruction. Both carbon variables dominate the first function, while δ15N most strongly influences the second. Independent support for the functions' ability to accurately classify individuals according to diet comes from a small sample of experimental rats, which cluster as expected from their diets. The new model also provides a statistical basis for distinguishing between food sources with similar isotopic signatures, as in a previously analyzed archaeological population from Saipan (see Ambrose et al.: AJPA 104(1997) 343-361). Our model suggests that the Saipan islanders' 13C-enriched signal derives mainly from sugarcane, not seaweed. Further development and application of this model can similarly improve dietary reconstructions in archaeological, paleontological, and primatological contexts. Am J Phys Anthropol, 2012. © 2011 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.21653" xmlns="http://purl.org/rss/1.0/"><title>Mutual mate choice in a female-dominant and sexually monomorphic primate</title><link>http://dx.doi.org/10.1002%2Fajpa.21653</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Mutual mate choice in a female-dominant and sexually monomorphic primate</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Doris Gomez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elise Huchard</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pierre-Yves Henry</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Martine Perret</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.21653</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.21653</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.21653</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">370</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">379</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Sexual dimorphism is common in polygynous species, where intrasexual competition is often thought to drive the evolution of large male body size, and in turn, male behavioral dominance over females. In Madagascar, the entire lemur radiation, which embraces diverse mating systems, lacks sexual dimorphism and exhibits frequent female dominance over males. The evolution of such morphological and behavioral peculiarities, often referred to as “the lemur syndrome,” has proven difficult to understand. Among other hypotheses, a potential role of intersexual selection has been repeatedly proposed but hardly ever tested. Here, we investigate whether female choice favors small and compliant males, and whether male choice favors large females in captive gray mouse lemurs (<em>Microcebus murinus</em>). Detailed analysis of a combination of behavioral observations and hormonal data available for both sexes shows that (1) females accept more matings from males with higher fighting abilities, (2) males adjust their investment in intrasexual competition to female fertility, and (3) both male and female strategies are weakly influenced by the body mass of potential partners, in directions contradicting our predictions. These results do not suggest a prominent role of intersexual selection in the evolution and maintenance of the lemur syndrome but rather point to alternative mechanisms relating to male–male competition, specifically highlighting an absence of relationship between male body mass and fighting ability. Finally, our findings add to the growing body of evidence suggesting flexible sex roles, by showing the expression of mutual mate choice in a female-dominant, sexually monomorphic and promiscuous primate. Am J Phys Anthropol, 2012. © 2011 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Sexual dimorphism is common in polygynous species, where intrasexual competition is often thought to drive the evolution of large male body size, and in turn, male behavioral dominance over females. In Madagascar, the entire lemur radiation, which embraces diverse mating systems, lacks sexual dimorphism and exhibits frequent female dominance over males. The evolution of such morphological and behavioral peculiarities, often referred to as “the lemur syndrome,” has proven difficult to understand. Among other hypotheses, a potential role of intersexual selection has been repeatedly proposed but hardly ever tested. Here, we investigate whether female choice favors small and compliant males, and whether male choice favors large females in captive gray mouse lemurs (Microcebus murinus). Detailed analysis of a combination of behavioral observations and hormonal data available for both sexes shows that (1) females accept more matings from males with higher fighting abilities, (2) males adjust their investment in intrasexual competition to female fertility, and (3) both male and female strategies are weakly influenced by the body mass of potential partners, in directions contradicting our predictions. These results do not suggest a prominent role of intersexual selection in the evolution and maintenance of the lemur syndrome but rather point to alternative mechanisms relating to male–male competition, specifically highlighting an absence of relationship between male body mass and fighting ability. Finally, our findings add to the growing body of evidence suggesting flexible sex roles, by showing the expression of mutual mate choice in a female-dominant, sexually monomorphic and promiscuous primate. Am J Phys Anthropol, 2012. © 2011 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22000" xmlns="http://purl.org/rss/1.0/"><title>Surnames in Chile: A study of the population of Chile through isonymy</title><link>http://dx.doi.org/10.1002%2Fajpa.22000</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Surnames in Chile: A study of the population of Chile through isonymy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Barrai</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Rodriguez-Larralde</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Dipierri</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Alfaro</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Acevedo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Mamolini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Sandri</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Carrieri</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Scapoli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22000</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22000</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22000</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">380</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">388</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In Chile, the Hispanic dual surname system is used. To describe the isonymic structure of this country, the distribution of 16,277,255 surnames of 8,178,209 persons was studied in the 15 regions, the 54 provinces, and the 346 communes of the nation. The number of different surnames found was 72,667. Effective surname number (Fisher's α) for the entire country was 309.0, the average for regions was 240.8 ± 17.6, for provinces 209.2 ± 8.9, and for communes 178.7 ± 4.7. These values display a variation of inbreeding between administrative levels in the Chilean population, which can be attributed to the ‘Prefecture effect’ of Nei and Imaizumi. Matrices of isonymic distances between units within administrative levels were tested for correlation with geographic distance. The correlations were highest for provinces (<em>r</em> = 0.630 ± 0.019 for Euclidean distance) and lowest for communes (<em>r</em> = 0.366 ± 0.009 for Lasker's). The geographical distribution of the first three-dimensions of the Euclidean distance matrix suggests that population diffusion may have taken place from the north of the country toward the center and south. The prevalence of European plus European-Amerindian (95.4%) over Amerindian ethnicity (4.6%, CIA World Factbook) is compatible with diffusion of Caucasian groups over a low-density area populated by indigenous groups. The significant excess of maternal over paternal indigenous surnames indicates some asymmetric mating between nonAmerindian and Amerindian Chileans. The available studies of Y-markers and mt-markers are in agreement with this asymmetry. In the present work, we investigate the Chilean population with the aim of detecting its structure through the study of isonymy (Crow and Mange,<a href="#bib9" rel="references:#bib9">1965</a>) in the three administrative levels of the nation, namely 15 regions, 54 provinces, and 346 communes. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>In Chile, the Hispanic dual surname system is used. To describe the isonymic structure of this country, the distribution of 16,277,255 surnames of 8,178,209 persons was studied in the 15 regions, the 54 provinces, and the 346 communes of the nation. The number of different surnames found was 72,667. Effective surname number (Fisher's α) for the entire country was 309.0, the average for regions was 240.8 ± 17.6, for provinces 209.2 ± 8.9, and for communes 178.7 ± 4.7. These values display a variation of inbreeding between administrative levels in the Chilean population, which can be attributed to the ‘Prefecture effect’ of Nei and Imaizumi. Matrices of isonymic distances between units within administrative levels were tested for correlation with geographic distance. The correlations were highest for provinces (r = 0.630 ± 0.019 for Euclidean distance) and lowest for communes (r = 0.366 ± 0.009 for Lasker's). The geographical distribution of the first three-dimensions of the Euclidean distance matrix suggests that population diffusion may have taken place from the north of the country toward the center and south. The prevalence of European plus European-Amerindian (95.4%) over Amerindian ethnicity (4.6%, CIA World Factbook) is compatible with diffusion of Caucasian groups over a low-density area populated by indigenous groups. The significant excess of maternal over paternal indigenous surnames indicates some asymmetric mating between nonAmerindian and Amerindian Chileans. The available studies of Y-markers and mt-markers are in agreement with this asymmetry. In the present work, we investigate the Chilean population with the aim of detecting its structure through the study of isonymy (Crow and Mange,1965) in the three administrative levels of the nation, namely 15 regions, 54 provinces, and 346 communes. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22001" xmlns="http://purl.org/rss/1.0/"><title>Adrenal androgen production in catarrhine primates and the evolution of adrenarche</title><link>http://dx.doi.org/10.1002%2Fajpa.22001</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Adrenal androgen production in catarrhine primates and the evolution of adrenarche</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robin M. Bernstein</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kirstin N. Sterner</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Derek E. Wildman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22001</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22001</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22001</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">389</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">400</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Adrenarche is a developmental event involving differentiation of the adrenal gland and production of adrenal androgens, and has been hypothesized to play a role in the extension of the preadolescent phase of human ontogeny. It remains unclear whether any nonhuman primate species shows a similar suite of endocrine, biochemical, and morphological changes as are encompassed by human adrenarche. Here, we report serum concentrations of the adrenal androgens dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS) measured in 698 cross-sectional and mixed longitudinal serum samples from catarrhine primates ranging from 0.6 to 47 years of age. DHEAS in <em>Pan</em> is most similar to that of humans in both age-related pattern and absolute levels, and a transient early increase appears to be present in <em>Gorilla</em>. DHEA levels are highest in <em>Cercocebus</em>, <em>Cercopithecus</em>, and <em>Macaca</em>. We also tested for evidence of adaptive evolution in six genes that code for proteins involved in DHEA/S synthesis. Our genetic analyses demonstrate the protein-coding regions of these genes are highly conserved among sampled primates. We describe a tandem gene duplication event probably mediated by a retrotransposon that resulted in two 3-β-hydroxysteroid dehydrogenase/Delta 5-Delta 4 genes (<em>HSD3B1</em> and <em>HSD3B2</em>) with tissue specific functions in catarrhines. In humans, <em>HSD3B</em>2 is expressed primarily in the adrenals, ovary, and testis, while <em>HSD3B1</em> is expressed in the placenta. Taken together, our findings suggest that while adrenarche has been suggested to be unique to hominoids, the evolutionary roots for this developmental stage are more ancient. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Adrenarche is a developmental event involving differentiation of the adrenal gland and production of adrenal androgens, and has been hypothesized to play a role in the extension of the preadolescent phase of human ontogeny. It remains unclear whether any nonhuman primate species shows a similar suite of endocrine, biochemical, and morphological changes as are encompassed by human adrenarche. Here, we report serum concentrations of the adrenal androgens dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS) measured in 698 cross-sectional and mixed longitudinal serum samples from catarrhine primates ranging from 0.6 to 47 years of age. DHEAS in Pan is most similar to that of humans in both age-related pattern and absolute levels, and a transient early increase appears to be present in Gorilla. DHEA levels are highest in Cercocebus, Cercopithecus, and Macaca. We also tested for evidence of adaptive evolution in six genes that code for proteins involved in DHEA/S synthesis. Our genetic analyses demonstrate the protein-coding regions of these genes are highly conserved among sampled primates. We describe a tandem gene duplication event probably mediated by a retrotransposon that resulted in two 3-β-hydroxysteroid dehydrogenase/Delta 5-Delta 4 genes (HSD3B1 and HSD3B2) with tissue specific functions in catarrhines. In humans, HSD3B2 is expressed primarily in the adrenals, ovary, and testis, while HSD3B1 is expressed in the placenta. Taken together, our findings suggest that while adrenarche has been suggested to be unique to hominoids, the evolutionary roots for this developmental stage are more ancient. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22002" xmlns="http://purl.org/rss/1.0/"><title>Testing Bergmann's rule and the resource seasonality hypothesis in Malagasy primates using GIS-based climate data</title><link>http://dx.doi.org/10.1002%2Fajpa.22002</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Testing Bergmann's rule and the resource seasonality hypothesis in Malagasy primates using GIS-based climate data</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jason M. Kamilar</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kathleen M. Muldoon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shawn M. Lehman</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">James P. Herrera</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22002</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22002</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22002</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">401</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">408</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We tested four major hypotheses on the ecological aspects of body mass variation in extant Malagasy strepsirrhines: thermoregulation, resource seasonality/scarcity, resource quality, and primary productivity. These biogeographic hypotheses focus on the ecological aspects of body mass variation, largely ignoring the role of phylogeny for explaining body mass variation within lineages. We tested the independent effects of climate and resource-related variables on variation in body mass among Malagasy primates using recently developed comparative methods that account for phylogenetic history and spatial autocorrelation. We extracted data on lemur body mass and climate variables for a total of 43 species from 39 sites. Climatic data were obtained from the WorldClim database, which is based on climate data from weather stations compiled around the world. Using generalized linear models that incorporate parameters to account for phylogenetic and spatial autocorrelation, we found that diet and climate variables were weak predictors of lemur body mass. Moreover, there was a strong phylogenetic effect relative to the effects of space on lemur body mass in all models. Thus, we failed to find support for any of the four hypotheses on patterns of geography and body mass in extant strepsirrhines. Our results indicate that body mass has been conserved since early in the evolutionary history of each genus, while species diversified into different environmental niches. Our findings are in contrast to some previous studies that have suggested resource and climate related effects on body mass, though these studies have examined this question at different taxonomic and/or geographic scales. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>We tested four major hypotheses on the ecological aspects of body mass variation in extant Malagasy strepsirrhines: thermoregulation, resource seasonality/scarcity, resource quality, and primary productivity. These biogeographic hypotheses focus on the ecological aspects of body mass variation, largely ignoring the role of phylogeny for explaining body mass variation within lineages. We tested the independent effects of climate and resource-related variables on variation in body mass among Malagasy primates using recently developed comparative methods that account for phylogenetic history and spatial autocorrelation. We extracted data on lemur body mass and climate variables for a total of 43 species from 39 sites. Climatic data were obtained from the WorldClim database, which is based on climate data from weather stations compiled around the world. Using generalized linear models that incorporate parameters to account for phylogenetic and spatial autocorrelation, we found that diet and climate variables were weak predictors of lemur body mass. Moreover, there was a strong phylogenetic effect relative to the effects of space on lemur body mass in all models. Thus, we failed to find support for any of the four hypotheses on patterns of geography and body mass in extant strepsirrhines. Our results indicate that body mass has been conserved since early in the evolutionary history of each genus, while species diversified into different environmental niches. Our findings are in contrast to some previous studies that have suggested resource and climate related effects on body mass, though these studies have examined this question at different taxonomic and/or geographic scales. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22008" xmlns="http://purl.org/rss/1.0/"><title>Evolutionary disequilibrium and activity period in primates: A bayesian phylogenetic approach</title><link>http://dx.doi.org/10.1002%2Fajpa.22008</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evolutionary disequilibrium and activity period in primates: A bayesian phylogenetic approach</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Randi H. Griffin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luke J. Matthews</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Charles L. Nunn</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22008</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22008</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22008</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">409</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">416</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Activity period plays a central role in studies of primate origins and adaptations, yet fundamental questions remain concerning the evolutionary history of primate activity period. Lemurs are of particular interest because they display marked variation in activity period, with some species exhibiting completely nocturnal or diurnal lifestyles, and others distributing activity throughout the 24-h cycle (i.e., cathemerality). Some lines of evidence suggest that cathemerality in lemurs is a recent and transient evolutionary state (i.e., the evolutionary disequilibrium hypothesis), while other studies indicate that cathemerality is a stable evolutionary strategy with a more ancient history. Debate also surrounds activity period in early primate evolution, with some recent studies casting doubt on the traditional hypothesis that basal primates were nocturnal. Here, we used Bayesian phylogenetic methods to reconstruct activity period at key points in primate evolution. Counter to the evolutionary disequilibrium hypothesis, the most recent common ancestor of <em>Eulemur</em> was reconstructed as cathemeral at ∼9–13 million years ago, indicating that cathemerality in lemurs is a stable evolutionary strategy. We found strong evidence favoring a nocturnal ancestor for all primates, strepsirrhines and lemurs, which adds to previous findings based on parsimony by providing quantitative support for these reconstructions. Reconstructions for the haplorrhine ancestor were more equivocal, but diurnality was favored for simian primates. We discuss the implications of our models for the evolutionary disequilibrium hypothesis, and we identify avenues for future research that would provide new insights into the evolution of cathemerality in lemurs. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Activity period plays a central role in studies of primate origins and adaptations, yet fundamental questions remain concerning the evolutionary history of primate activity period. Lemurs are of particular interest because they display marked variation in activity period, with some species exhibiting completely nocturnal or diurnal lifestyles, and others distributing activity throughout the 24-h cycle (i.e., cathemerality). Some lines of evidence suggest that cathemerality in lemurs is a recent and transient evolutionary state (i.e., the evolutionary disequilibrium hypothesis), while other studies indicate that cathemerality is a stable evolutionary strategy with a more ancient history. Debate also surrounds activity period in early primate evolution, with some recent studies casting doubt on the traditional hypothesis that basal primates were nocturnal. Here, we used Bayesian phylogenetic methods to reconstruct activity period at key points in primate evolution. Counter to the evolutionary disequilibrium hypothesis, the most recent common ancestor of Eulemur was reconstructed as cathemeral at ∼9–13 million years ago, indicating that cathemerality in lemurs is a stable evolutionary strategy. We found strong evidence favoring a nocturnal ancestor for all primates, strepsirrhines and lemurs, which adds to previous findings based on parsimony by providing quantitative support for these reconstructions. Reconstructions for the haplorrhine ancestor were more equivocal, but diurnality was favored for simian primates. We discuss the implications of our models for the evolutionary disequilibrium hypothesis, and we identify avenues for future research that would provide new insights into the evolution of cathemerality in lemurs. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22009" xmlns="http://purl.org/rss/1.0/"><title>Enamel thickness in Bornean and Sumatran orangutan dentitions</title><link>http://dx.doi.org/10.1002%2Fajpa.22009</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Enamel thickness in Bornean and Sumatran orangutan dentitions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tanya M. Smith</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kornelius Kupczik</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zarin Machanda</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Matthew M. Skinner</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John P. Zermeno</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22009</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22009</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22009</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">417</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">426</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Dental enamel thickness has received considerable attention in ecological models of the adaptive significance of primate morphology. Several authors have theorized that the degree of enamel thickness may reflect selective pressures related to the consumption of fallback foods (dietary items that may require complex processing and/or have low nutritional value) during times of preferred food scarcity. Others have speculated that enamel thickness reflects selection during mastication of foods with particular material properties (i.e., toughness and hardness). Orangutans prefer ripe fruit when available, but show interspecific and sex differences in the consumption of fallback foods (bark, leaves, and figs) and other preferred foods (certain seeds). Bornean orangutans (<em>Pongo pygmaeus</em>) have also been reported to masticate more mechanically demanding foods than Sumatran orangutans (<em>Pongo abelii</em>). To test these ecological models, we assessed two-dimensional enamel thickness in orangutan full dentitions using established histological and virtual quantification methods. No significant differences in average enamel thickness (AET) were found between species. We found significant differences in the components of enamel thickness indices between sexes, with males showing greater enamel-dentine junction lengths and dentine core areas, and thus relatively thinner enamel than females. Comparisons of individuals of known sex and species revealed a dentition-wide trend for Bornean females to show greater AET than Sumatran females. Differences between small samples of males were less evident. These data provide only limited support for ecological explanations of enamel thickness patterns within great ape genera. Future studies of dietary ecology and enamel thickness should consider sex differences more systematically. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Dental enamel thickness has received considerable attention in ecological models of the adaptive significance of primate morphology. Several authors have theorized that the degree of enamel thickness may reflect selective pressures related to the consumption of fallback foods (dietary items that may require complex processing and/or have low nutritional value) during times of preferred food scarcity. Others have speculated that enamel thickness reflects selection during mastication of foods with particular material properties (i.e., toughness and hardness). Orangutans prefer ripe fruit when available, but show interspecific and sex differences in the consumption of fallback foods (bark, leaves, and figs) and other preferred foods (certain seeds). Bornean orangutans (Pongo pygmaeus) have also been reported to masticate more mechanically demanding foods than Sumatran orangutans (Pongo abelii). To test these ecological models, we assessed two-dimensional enamel thickness in orangutan full dentitions using established histological and virtual quantification methods. No significant differences in average enamel thickness (AET) were found between species. We found significant differences in the components of enamel thickness indices between sexes, with males showing greater enamel-dentine junction lengths and dentine core areas, and thus relatively thinner enamel than females. Comparisons of individuals of known sex and species revealed a dentition-wide trend for Bornean females to show greater AET than Sumatran females. Differences between small samples of males were less evident. These data provide only limited support for ecological explanations of enamel thickness patterns within great ape genera. Future studies of dietary ecology and enamel thickness should consider sex differences more systematically. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22010" xmlns="http://purl.org/rss/1.0/"><title>Stability or variation? Patterns of lactase gene and its enhancer region distributions in Brazilian Amerindians</title><link>http://dx.doi.org/10.1002%2Fajpa.22010</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Stability or variation? Patterns of lactase gene and its enhancer region distributions in Brazilian Amerindians</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Deise C. Friedrich</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sidia M. Callegari-Jacques</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Luiza Petzl-Erler</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luiza Tsuneto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francisco M. Salzano</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mara H. Hutz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22010</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22010</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22010</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">427</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">432</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Lactase persistence (LP) is the phenotypic trait in which lactase secretion is maintained during adulthood. LP is due to mutations in the <em>LCT</em> enhancer region, located 14-kb upstream of the gene. In Europeans, the −13910*T allele is associated with LP. In Africans this allele is rare while other mutations in this same region were related to LP. The <em>LCT</em> is highly polymorphic in human populations, but so far Brazilian Amerindians had not been investigated for these polymorphisms or for the presence of LP mutations. We describe the genetic diversity of the <em>LCT</em> region and the presence of LP enhancer mutations in four native Brazilian populations (Guarani-Kaiowá, Guarani–Ñandeva, Kaingang, and Xavante). Twelve polymorphisms were genotyped by PCR-based methods. The −13910*T allele varied from 0.5% in the Xavante to 7.6% in the Guarani–Ñandeva. These frequencies probably derive from European sources and they correlate with non-native admixture proportions previously estimated for these groups. But since admixture is virtually absent in the Xavante, we suggest that the presence of the LP allele could have been determined by a de novo mutation. No other mutations in the −14 kb enhancer region were found. The <em>LCT</em> was highly polymorphic in the present sample showing 15 haplotypes with a heterogeneous distribution among the four Amerindian populations. This diversity could be due to drift, as indicated by the neutrality test performed. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Lactase persistence (LP) is the phenotypic trait in which lactase secretion is maintained during adulthood. LP is due to mutations in the LCT enhancer region, located 14-kb upstream of the gene. In Europeans, the −13910*T allele is associated with LP. In Africans this allele is rare while other mutations in this same region were related to LP. The LCT is highly polymorphic in human populations, but so far Brazilian Amerindians had not been investigated for these polymorphisms or for the presence of LP mutations. We describe the genetic diversity of the LCT region and the presence of LP enhancer mutations in four native Brazilian populations (Guarani-Kaiowá, Guarani–Ñandeva, Kaingang, and Xavante). Twelve polymorphisms were genotyped by PCR-based methods. The −13910*T allele varied from 0.5% in the Xavante to 7.6% in the Guarani–Ñandeva. These frequencies probably derive from European sources and they correlate with non-native admixture proportions previously estimated for these groups. But since admixture is virtually absent in the Xavante, we suggest that the presence of the LP allele could have been determined by a de novo mutation. No other mutations in the −14 kb enhancer region were found. The LCT was highly polymorphic in the present sample showing 15 haplotypes with a heterogeneous distribution among the four Amerindian populations. This diversity could be due to drift, as indicated by the neutrality test performed. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22011" xmlns="http://purl.org/rss/1.0/"><title>Ancient-to-modern secular changes in Korean stature</title><link>http://dx.doi.org/10.1002%2Fajpa.22011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ancient-to-modern secular changes in Korean stature</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dong Hoon Shin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chang Seok Oh</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yi-Suk Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Young-il Hwang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22011</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22011</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">433</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">442</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Statural growth in human populations is a sensitive indicator of socio-economic well-being, and improvements in socio-economic status are reflected in secular increases in adult height. In the present study, we investigated the statures of historical Korean societies to show how stature changed over time. Applying Fujii's equation, derived from modern Japanese, to the measurement of femora removed from 15th- to 19th-century Joseon tombs, the average heights of Korean adults during the Joseon dynasty were estimated to be 161.1 ± 5.6 cm and 148.9 ± 4.6 cm for males and females, respectively. Plotting statures for successive historical societies against time revealed that Korean heights remained relatively unchanged through to the end of the 19th century, a pattern that differs from that seen in many Western countries in which stature transiently decreases after the Middle Ages. In contrast, a sharp increase in Korean stature was observed at the beginning of the 20th century, similar to trends seen in other nations (although exact timing varies in different countries). There were no accompanying changes of stature sexual dimorphism. The data reported in this study reflect the unique historical experience of Korea; the relative isolation of Joseon society, the late onset of modernization (at the end of the 19th century), and the later occurrence of industrialization (during the 1960s). Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Statural growth in human populations is a sensitive indicator of socio-economic well-being, and improvements in socio-economic status are reflected in secular increases in adult height. In the present study, we investigated the statures of historical Korean societies to show how stature changed over time. Applying Fujii's equation, derived from modern Japanese, to the measurement of femora removed from 15th- to 19th-century Joseon tombs, the average heights of Korean adults during the Joseon dynasty were estimated to be 161.1 ± 5.6 cm and 148.9 ± 4.6 cm for males and females, respectively. Plotting statures for successive historical societies against time revealed that Korean heights remained relatively unchanged through to the end of the 19th century, a pattern that differs from that seen in many Western countries in which stature transiently decreases after the Middle Ages. In contrast, a sharp increase in Korean stature was observed at the beginning of the 20th century, similar to trends seen in other nations (although exact timing varies in different countries). There were no accompanying changes of stature sexual dimorphism. The data reported in this study reflect the unique historical experience of Korea; the relative isolation of Joseon society, the late onset of modernization (at the end of the 19th century), and the later occurrence of industrialization (during the 1960s). Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22013" xmlns="http://purl.org/rss/1.0/"><title>The population genetics of quechuas, the largest native south american group: Autosomal sequences, SNPs, and microsatellites evidence high level of diversity</title><link>http://dx.doi.org/10.1002%2Fajpa.22013</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The population genetics of quechuas, the largest native south american group: Autosomal sequences, SNPs, and microsatellites evidence high level of diversity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marilia O. Scliar</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Giordano B. Soares-Souza</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Juliana Chevitarese</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Livia Lemos</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wagner C.S. Magalhães</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nelson J. Fagundes</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sandro L. Bonatto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Meredith Yeager</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stephen J. Chanock</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eduardo Tarazona-Santos</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22013</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22013</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22013</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">443</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">451</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Elucidating the pattern of genetic diversity for non-European populations is necessary to make the benefits of human genetics research available to individuals from these groups. In the era of large human genomic initiatives, Native American populations have been neglected, in particular, the Quechua, the largest South Amerindian group settled along the Andes. We characterized the genetic diversity of a Quechua population in a global setting, using autosomal noncoding sequences (nine unlinked loci for a total of 16 kb), 351 unlinked SNPs and 678 microsatellites and tested predictions of the model of the evolution of Native Americans proposed by (Tarazona-Santos et al.: Am J Hum Genet 68 (<a href="#bib60" rel="references:#bib60">2001</a>) 1485–1496). European admixture is &lt;5% and African ancestry is barely detectable in the studied population. The largest genetic distances were between African versus Quechua or Melanesian populations, which is concordant with the African origin of modern humans and the fact that South America was the last part of the world to be peopled. The diversity in the Quechua population is comparable with that of Eurasian populations, and the allele frequency spectrum based on resequencing data does not reflect a reduction in the proportion of rare alleles. Thus, the Quechua population is a large reservoir of common and rare genetic variants of South Amerindians. These results are consistent with and complement our evolutionary model of South Amerindians (Tarazona-Santos et al.: Am J Hum Genet 68 (<a href="#bib60" rel="references:#bib60">2001</a>) 1485–1496), proposed based on Y-chromosome data, which predicts high genomic diversity due to the high level of gene flow between Andean populations and their long-term effective population size. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Elucidating the pattern of genetic diversity for non-European populations is necessary to make the benefits of human genetics research available to individuals from these groups. In the era of large human genomic initiatives, Native American populations have been neglected, in particular, the Quechua, the largest South Amerindian group settled along the Andes. We characterized the genetic diversity of a Quechua population in a global setting, using autosomal noncoding sequences (nine unlinked loci for a total of 16 kb), 351 unlinked SNPs and 678 microsatellites and tested predictions of the model of the evolution of Native Americans proposed by (Tarazona-Santos et al.: Am J Hum Genet 68 (2001) 1485–1496). European admixture is &lt;5% and African ancestry is barely detectable in the studied population. The largest genetic distances were between African versus Quechua or Melanesian populations, which is concordant with the African origin of modern humans and the fact that South America was the last part of the world to be peopled. The diversity in the Quechua population is comparable with that of Eurasian populations, and the allele frequency spectrum based on resequencing data does not reflect a reduction in the proportion of rare alleles. Thus, the Quechua population is a large reservoir of common and rare genetic variants of South Amerindians. These results are consistent with and complement our evolutionary model of South Amerindians (Tarazona-Santos et al.: Am J Hum Genet 68 (2001) 1485–1496), proposed based on Y-chromosome data, which predicts high genomic diversity due to the high level of gene flow between Andean populations and their long-term effective population size. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22015" xmlns="http://purl.org/rss/1.0/"><title>Three-dimensional evaluation of root canal morphology in lower second premolars of early and middle pleistocene human populations from atapuerca (Burgos, Spain)</title><link>http://dx.doi.org/10.1002%2Fajpa.22015</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Three-dimensional evaluation of root canal morphology in lower second premolars of early and middle pleistocene human populations from atapuerca (Burgos, Spain)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leyre Prado-Simón</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">María Martinón-Torres</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pilar Baca</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anthony J. Olejniczak</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Aida Gómez-Robles</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">María Lapresa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Juan Luis Arsuaga</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">José María Bermúdez de Castro</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22015</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22015</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22015</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">452</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">461</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The aim of this study is to describe the morphology of the roots and root canals of permanent lower second premolars (LP4s) with fully developed roots of five hominin groups: <em>Homo</em> sp. (ATE9-1 specimen) from Atapuerca-Sima del Elefante locality, <em>H. antecessor</em> (ATD6-4 and ATD6-125) from Atapuerca-Gran Dolina TD6 locality, <em>H. heidelbergensis</em> from Atapuerca-Sima de los Huesos locality, <em>H. neanderthalensis</em> from Krapina, Regourdou, and Abri Bourgeois-Delaunay localities, and two contemporary <em>H. sapiens</em> groups. The teeth were scanned by means of microtomography. The roots were divided into three virtual segments by three planes: cemento-enamel junction (CEJ), mid-root (MR), and mid-apex (MA). Volumetric and planar direct measurements of the whole teeth and each segment were taken. Descriptive statistical analyses and nonparametric Mann-Whiney test were performed to test for significant differences (<em>P</em> &lt; 0.025) between groups. ATE9-1 and Gran Dolina-TD6 fossils present intricate radicular complexes that might be transitional between the morphologies of <em>Australopithecus robustus</em> and African early <em>Homo</em> and the derived conditions typically found in later <em>Homo</em>. In <em>H. neanderthalensis</em> and <em>H. heidelbergensis</em>, the root canals are wide, with small apical convergence. This trait is particularly pronounced in the Sima de los Huesos sample which may reflect a particularity of this population. Our study demonstrates the potential of hominin roots and root canals as untapped sources of taxonomic information when the tooth crown is fragmented. Future studies, including more fossil specimens and species will shed light in the polarity of the morphologies observed. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>The aim of this study is to describe the morphology of the roots and root canals of permanent lower second premolars (LP4s) with fully developed roots of five hominin groups: Homo sp. (ATE9-1 specimen) from Atapuerca-Sima del Elefante locality, H. antecessor (ATD6-4 and ATD6-125) from Atapuerca-Gran Dolina TD6 locality, H. heidelbergensis from Atapuerca-Sima de los Huesos locality, H. neanderthalensis from Krapina, Regourdou, and Abri Bourgeois-Delaunay localities, and two contemporary H. sapiens groups. The teeth were scanned by means of microtomography. The roots were divided into three virtual segments by three planes: cemento-enamel junction (CEJ), mid-root (MR), and mid-apex (MA). Volumetric and planar direct measurements of the whole teeth and each segment were taken. Descriptive statistical analyses and nonparametric Mann-Whiney test were performed to test for significant differences (P &lt; 0.025) between groups. ATE9-1 and Gran Dolina-TD6 fossils present intricate radicular complexes that might be transitional between the morphologies of Australopithecus robustus and African early Homo and the derived conditions typically found in later Homo. In H. neanderthalensis and H. heidelbergensis, the root canals are wide, with small apical convergence. This trait is particularly pronounced in the Sima de los Huesos sample which may reflect a particularity of this population. Our study demonstrates the potential of hominin roots and root canals as untapped sources of taxonomic information when the tooth crown is fragmented. Future studies, including more fossil specimens and species will shed light in the polarity of the morphologies observed. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22024" xmlns="http://purl.org/rss/1.0/"><title>Allometry of head and body size in holocene foragers of the south african cape</title><link>http://dx.doi.org/10.1002%2Fajpa.22024</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Allometry of head and body size in holocene foragers of the south african cape</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Helen K. Kurki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Susan Pfeiffer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Deano D. Stynder</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22024</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22024</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22024</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Research Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">462</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">471</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Opportunities to assess morphological allometry in small-bodied human populations are rare. The foragers of the Later Stone Age of the South African Cape are characteristically small-bodied. Previous studies have shown that during the period of ca. 3500 to 2000 years BP (uncalibrated <sup>14</sup>C dates), the regional population shows transient reduced stature, body mass, and cranial size, a pattern that has been tentatively tied to demographic pressure on resources. This study examines the relationships among cranial size (centroid size) and body size (femoral length, femoral head diameter, and bi-iliac breadth) during the second half of the Holocene (<em>N</em> = 62). Reduced major axis regression indicates negative allometry of cranial centroid size with body size. Residuals (from ordinary least squares regression of cranial centroid size on body size) are regressed on radiocarbon date to examine temporal changes in the relationship between cranial and body size. Cranial and pelvic sizes are most conserved through time, while more ancient skeletons possess shorter femora and smaller femoral heads. The relationship between cranial centroid size and femoral length shows larger and more variable residuals at more recent dates, indicating a greater or more variable disassociation between cranial size and stature relative to more ancient skeletons. A similar, but nonsignificant relationship exists between cranial size and bi-iliac breadth. These results provide insights into the use of aspects of body size and proportionality in the assessment of health in past populations. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Opportunities to assess morphological allometry in small-bodied human populations are rare. The foragers of the Later Stone Age of the South African Cape are characteristically small-bodied. Previous studies have shown that during the period of ca. 3500 to 2000 years BP (uncalibrated 14C dates), the regional population shows transient reduced stature, body mass, and cranial size, a pattern that has been tentatively tied to demographic pressure on resources. This study examines the relationships among cranial size (centroid size) and body size (femoral length, femoral head diameter, and bi-iliac breadth) during the second half of the Holocene (N = 62). Reduced major axis regression indicates negative allometry of cranial centroid size with body size. Residuals (from ordinary least squares regression of cranial centroid size on body size) are regressed on radiocarbon date to examine temporal changes in the relationship between cranial and body size. Cranial and pelvic sizes are most conserved through time, while more ancient skeletons possess shorter femora and smaller femoral heads. The relationship between cranial centroid size and femoral length shows larger and more variable residuals at more recent dates, indicating a greater or more variable disassociation between cranial size and stature relative to more ancient skeletons. A similar, but nonsignificant relationship exists between cranial size and bi-iliac breadth. These results provide insights into the use of aspects of body size and proportionality in the assessment of health in past populations. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.21657" xmlns="http://purl.org/rss/1.0/"><title>Brief communication: Two human fossil deciduous molars from the sangiran dome (Java, Indonesia): Outer and inner morphology</title><link>http://dx.doi.org/10.1002%2Fajpa.21657</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Brief communication: Two human fossil deciduous molars from the sangiran dome (Java, Indonesia): Outer and inner morphology</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Clément Zanolli</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luca Bondioli</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lucia Mancini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Arnaud Mazurier</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Harry Widianto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roberto Macchiarelli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.21657</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.21657</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.21657</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Communication</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">472</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">481</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Currently, the human deciduous dental record from the Pleistocene deposits of the Sangiran Dome, Java, consists of only eight specimens. Here we report two deciduous crowns collected near the village of Pucung. While their precise geo-chronological context remains unknown, a provenance from the Early–Middle Pleistocene Kabuh Formation, or from the Early Pleistocene “Grenzbank Zone,” is very likely. These isolated specimens consist of an upper first molar (PCG.1) and a lower second molar (PCG.2). Taxonomic discrimination of the Indonesian tooth record is difficult because of the convergence in crown size and appearance between <em>Pongo</em> and <em>Homo</em>. Accordingly, as PCG.2 still bears a concretion masking most of its features, we coupled the outer analysis of the two specimens with an investigation of their inner morphology. In addition to external characteristics, virtual imaging and quantitative assessment of inner morphology and tissue proportions support an attribution to the taxon <em>Homo</em>, and we preliminary allocate both specimens to<em>H. erectus</em>. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Currently, the human deciduous dental record from the Pleistocene deposits of the Sangiran Dome, Java, consists of only eight specimens. Here we report two deciduous crowns collected near the village of Pucung. While their precise geo-chronological context remains unknown, a provenance from the Early–Middle Pleistocene Kabuh Formation, or from the Early Pleistocene “Grenzbank Zone,” is very likely. These isolated specimens consist of an upper first molar (PCG.1) and a lower second molar (PCG.2). Taxonomic discrimination of the Indonesian tooth record is difficult because of the convergence in crown size and appearance between Pongo and Homo. Accordingly, as PCG.2 still bears a concretion masking most of its features, we coupled the outer analysis of the two specimens with an investigation of their inner morphology. In addition to external characteristics, virtual imaging and quantitative assessment of inner morphology and tissue proportions support an attribution to the taxon Homo, and we preliminary allocate both specimens toH. erectus. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22021" xmlns="http://purl.org/rss/1.0/"><title>Brief communication: A preliminary study on the influence of physical fruit traits on fruit handling and seed fate by white-handed titi monkeys (Callicebus lugens)</title><link>http://dx.doi.org/10.1002%2Fajpa.22021</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Brief communication: A preliminary study on the influence of physical fruit traits on fruit handling and seed fate by white-handed titi monkeys (Callicebus lugens)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Silvia J. Alvarez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eckhard W. Heymann</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22021</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22021</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22021</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Communication</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">482</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">488</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><em>Callicebus</em> and the pitheciins are closely related; however, differences in their diets and dental morphology suggest that they differ in the use of mechanically protected food. We describe physical traits of fruits consumed by white-handed titi monkeys (<em>Callicebus lugens</em>) and determine their influence on fruit part selection and immediate seed fate after fruit handling. We tested two hypotheses about the effects of mechanical fruit traits on fruit part selection and seed fate: (1) fruits selected for seed consumption are harder than fruits selected for their fleshy parts and (2) consumed seeds are softer than seeds with other fates. In addition, we analyzed the influence of other physical fruit traits on fruit part selection and seed fate. <em>C. lugens</em> included 69 species in its diet, from which it mainly consumed their fleshy parts. It also consumed seeds, alone or with fleshy fruit parts, but most of them ended up close to parent trees after being dropped or spat out. The first hypothesis was supported while the second was rejected, indicating that <em>C. lugens</em> tends to rely on hard fruits for obtaining seeds, while seed hardness had no influence on fruit part selection and seed fate, contrasting with the pattern reported for <em>Pithecia</em> and <em>Chiropotes</em> in other studies. Ripeness was the most influential factor for fruit part and seed fate discrimination. Results suggest a tendency to sclerocarpic foraging in <em>C. lugens</em> when feeding on seeds. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Callicebus and the pitheciins are closely related; however, differences in their diets and dental morphology suggest that they differ in the use of mechanically protected food. We describe physical traits of fruits consumed by white-handed titi monkeys (Callicebus lugens) and determine their influence on fruit part selection and immediate seed fate after fruit handling. We tested two hypotheses about the effects of mechanical fruit traits on fruit part selection and seed fate: (1) fruits selected for seed consumption are harder than fruits selected for their fleshy parts and (2) consumed seeds are softer than seeds with other fates. In addition, we analyzed the influence of other physical fruit traits on fruit part selection and seed fate. C. lugens included 69 species in its diet, from which it mainly consumed their fleshy parts. It also consumed seeds, alone or with fleshy fruit parts, but most of them ended up close to parent trees after being dropped or spat out. The first hypothesis was supported while the second was rejected, indicating that C. lugens tends to rely on hard fruits for obtaining seeds, while seed hardness had no influence on fruit part selection and seed fate, contrasting with the pattern reported for Pithecia and Chiropotes in other studies. Ripeness was the most influential factor for fruit part and seed fate discrimination. Results suggest a tendency to sclerocarpic foraging in C. lugens when feeding on seeds. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22022" xmlns="http://purl.org/rss/1.0/"><title>Brief communication: Radiographic study of metatarsal one basal epiphyseal fusion: A note of caution on age determination</title><link>http://dx.doi.org/10.1002%2Fajpa.22022</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Brief communication: Radiographic study of metatarsal one basal epiphyseal fusion: A note of caution on age determination</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elizabeth Weiss</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeremy DeSilva</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bernhard Zipfel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22022</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22022</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22022</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Brief Communication</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">489</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">492</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study examines radiographs of first metatarsals of 131 individuals from age 17–88 years to determine whether internal basal epiphyseal lines may be visible past the age of metatarsal fusion, which usually occurs between 14 and 16 years of age (Scheuer and Black: The juvenile skeleton. San Diego: Elsevier Academic Press,<a href="#bib16" rel="references:#bib16">2004</a>). In 29% (38 out of 131) of the radiographed first metatarsals (MT1s) the basal epiphyseal scar is visible, including in one individual who was 80 years old. Statistically, there was no relationship between the loss of the epiphyseal scar and age. Thus, the presence of the epiphyseal scar does not necessarily indicate subadult age. These data suggest that OH 8's radiographically visible basal epiphyseal line has no bearing on whether it is a subadult or not. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>This study examines radiographs of first metatarsals of 131 individuals from age 17–88 years to determine whether internal basal epiphyseal lines may be visible past the age of metatarsal fusion, which usually occurs between 14 and 16 years of age (Scheuer and Black: The juvenile skeleton. San Diego: Elsevier Academic Press,2004). In 29% (38 out of 131) of the radiographed first metatarsals (MT1s) the basal epiphyseal scar is visible, including in one individual who was 80 years old. Statistically, there was no relationship between the loss of the epiphyseal scar and age. Thus, the presence of the epiphyseal scar does not necessarily indicate subadult age. These data suggest that OH 8's radiographically visible basal epiphyseal line has no bearing on whether it is a subadult or not. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22018" xmlns="http://purl.org/rss/1.0/"><title>Technical note: Comparison of the maresh reference data with the who international standard for normal growth in healthy children</title><link>http://dx.doi.org/10.1002%2Fajpa.22018</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Technical note: Comparison of the maresh reference data with the who international standard for normal growth in healthy children</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael A. Schillaci</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H.P.S. Sachdev</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Santosh K. Bhargava</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22018</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22018</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22018</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Technical Note</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">493</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">498</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The Maresh reference data on stature and long bone lengths in a sample of healthy middle-class children from Denver, Colorado [Maresh: Am J Dis Child 66 (<a href="#bib13" rel="references:#bib13">1943</a>) 227–257; Maresh: Am J Dis Child 89 (<a href="#bib15" rel="references:#bib15">1955</a>) 725–742; Maresh: Human growth and development (<a href="#bib19" rel="references:#bib19">1970</a>) p 155–200], have been used extensively by biological anthropologists to estimate juvenile age and body size using skeletal elements and to assess growth in skeletal series from different ethnic populations or archaeological cultural groups. How well these data reflect the potentially diverse growth patterns of healthy human populations from different geographic areas is unknown. Similarly, the efficacy of using the Maresh reference data to estimate stunting prevalence in prehistoric populations is unknown. This report presents the results from a comparison of the Maresh data on supine length and standing height to the World Health Organization (WHO) international child growth standard. The WHO growth standard is meant to depict typical human growth under optimal conditions and can be used to assess children worldwide, regardless of ethnicity and socioeconomic status. The results from this comparison indicate that although the Maresh reference data generally conform to the WHO standard, reflecting a normal human growth pattern, and therefore serve as a suitable reference for comparative studies of growth patterns, these reference data are not suitable for estimating stunting prevalence. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>The Maresh reference data on stature and long bone lengths in a sample of healthy middle-class children from Denver, Colorado [Maresh: Am J Dis Child 66 (1943) 227–257; Maresh: Am J Dis Child 89 (1955) 725–742; Maresh: Human growth and development (1970) p 155–200], have been used extensively by biological anthropologists to estimate juvenile age and body size using skeletal elements and to assess growth in skeletal series from different ethnic populations or archaeological cultural groups. How well these data reflect the potentially diverse growth patterns of healthy human populations from different geographic areas is unknown. Similarly, the efficacy of using the Maresh reference data to estimate stunting prevalence in prehistoric populations is unknown. This report presents the results from a comparison of the Maresh data on supine length and standing height to the World Health Organization (WHO) international child growth standard. The WHO growth standard is meant to depict typical human growth under optimal conditions and can be used to assess children worldwide, regardless of ethnicity and socioeconomic status. The results from this comparison indicate that although the Maresh reference data generally conform to the WHO standard, reflecting a normal human growth pattern, and therefore serve as a suitable reference for comparative studies of growth patterns, these reference data are not suitable for estimating stunting prevalence. Am J Phys Anthropol 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22012" xmlns="http://purl.org/rss/1.0/"><title>Technical note: Interpreting stable carbon isotopes in human tooth enamel: An examination of tissue spacings from South Africa</title><link>http://dx.doi.org/10.1002%2Fajpa.22012</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Technical note: Interpreting stable carbon isotopes in human tooth enamel: An examination of tissue spacings from South Africa</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emma Loftus</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Judith Sealy</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22012</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22012</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22012</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Technical Note</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">499</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">507</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Stable isotope analysis of skeletal tissues is widely used in archeology and paleoanthropology to reconstruct diet. In material that is poorly preserved or very old, the tissue of choice is frequently tooth enamel, since this is less susceptible to diagenesis. The relationships between carbon isotope ratios in tooth enamel (δ<sup>13</sup>C<sub>enamel</sub>), bone collagen (δ<sup>13</sup>C<sub>collagen</sub>), and bone apatite (δ<sup>13</sup>C<sub>bone apatite</sub>) are, however, not well understood. To elucidate these, we have measured all three indicators in archeological humans from the western and southern Cape coastal regions of South Africa. The correlation between δ<sup>13</sup>C<sub>enamel</sub> and δ<sup>13</sup>C<sub>collagen</sub> is good (<em>R</em><sup>2</sup> = 0.71 if two outliers are excluded, <em>n</em> = 79). The correlation between δ<sup>13</sup>C<sub>enamel</sub> and δ<sup>13</sup>C<sub>bone apatite</sub> is weaker (<em>R</em><sup>2</sup>= 0.37, <em>n</em> = 33) possibly due to bone diagenesis. No systematic offset between δ<sup>13</sup>C<sub>bone apatite</sub> and δ<sup>13</sup>C<sub>enamel</sub> was observed in this sample of archeological humans. Intertooth comparisons of δ<sup>13</sup>C<sub>enamel</sub> in three individuals showed little variation, despite the different ages of crown formation. Carbon isotope ratios in both enamel and bone collagen are good proxies for δ<sup>13</sup>C<sub>diet</sub>. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</p></div>]]></content:encoded><description>Stable isotope analysis of skeletal tissues is widely used in archeology and paleoanthropology to reconstruct diet. In material that is poorly preserved or very old, the tissue of choice is frequently tooth enamel, since this is less susceptible to diagenesis. The relationships between carbon isotope ratios in tooth enamel (δ13Cenamel), bone collagen (δ13Ccollagen), and bone apatite (δ13Cbone apatite) are, however, not well understood. To elucidate these, we have measured all three indicators in archeological humans from the western and southern Cape coastal regions of South Africa. The correlation between δ13Cenamel and δ13Ccollagen is good (R2 = 0.71 if two outliers are excluded, n = 79). The correlation between δ13Cenamel and δ13Cbone apatite is weaker (R2= 0.37, n = 33) possibly due to bone diagenesis. No systematic offset between δ13Cbone apatite and δ13Cenamel was observed in this sample of archeological humans. Intertooth comparisons of δ13Cenamel in three individuals showed little variation, despite the different ages of crown formation. Carbon isotope ratios in both enamel and bone collagen are good proxies for δ13Cdiet. Am J Phys Anthropol, 2012. © 2012 Wiley Periodicals, Inc.</description></item><item rdf:about="http://dx.doi.org/10.1002%2Fajpa.22004" xmlns="http://purl.org/rss/1.0/"><title>Book review</title><link>http://dx.doi.org/10.1002%2Fajpa.22004</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Book review</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Markus Bastir</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-03-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1002/ajpa.22004</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1002/ajpa.22004</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1002%2Fajpa.22004</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Book Review</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">508</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">509</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item></rdf:RDF>
