Literature DB >> 7856764

Craniometric variation, genetic theory, and modern human origins.

J H Relethford1, H C Harpending.   

Abstract

Recent controversies surrounding models of modern human origins have focused on among-group variation, particularly the reconstruction of phylogenetic trees from mitochondrial DNA (mtDNA) and the dating of population divergence. Problems in tree estimation have been seen as weakening the case for a replacement model and favoring a multiregional evolution model. There has been less discussion of patterns of within-group variation, although the mtDNA evidence has consistently shown the greatest diversity within African populations. Problems of interpretation abound given the numerous factors that can influence within-group variation, including the possibility of earlier divergence, differences in population size, patterns of population expansion, and variation in migration rates. We present a model of within-group phenotypic variation and apply it to a large set of craniometric data representing major Old World geographic regions (57 measurements for 1,159 cases in four regions: Europe, Sub-Saharan Africa, Australasia, and the Far East). The model predicts a linear relationship between variation within populations (the average within-group variance) and variation between populations (the genetic distance of populations to pooled phenotypic means). On a global level this relationship should hold if the long-term effective population sizes of each region are correctly specified. Other potential effects on within-group variation are accounted for by the model. Comparison of observed and expected variances under the assumption of equal effective sizes for four regions indicates significantly greater within-group variation in Africa and significantly less within-group variation in Europe. These results suggest that the long-term effective population size was greatest in Africa. Closer examination of the model suggests that the long-term African effective size was roughly three times that of any other geographic region. Using these estimates of relative population size, we present a method for analyzing ancient population structure, which provides estimates of ancient migration. This method allows us to reconstruct migration history between geographic regions after adjustment for the effect of genetic drift on interpopulational distances. Our results show a clear isolation of Africa from other regions. We then present a method that allows direct estimation of the ancient migration matrix, thus providing us with information on the actual extent of interregional migration. These methods also provide estimates of time frames necessary to reach genetic equilibrium. The ultimate goal is extracting as much information from present-day patterns of human variation relevant to issues of human origins.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7856764     DOI: 10.1002/ajpa.1330950302

Source DB:  PubMed          Journal:  Am J Phys Anthropol        ISSN: 0002-9483            Impact factor:   2.868


  22 in total

1.  The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data.

Authors:  L B Jorde; W S Watkins; M J Bamshad; M E Dixon; C E Ricker; M T Seielstad; M A Batzer
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

2.  More on the X files.

Authors:  R M Harding
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

3.  Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.

Authors:  S A Tishkoff; A J Pakstis; M Stoneking; J R Kidd; G Destro-Bisol; A Sanjantila; R B Lu; A S Deinard; G Sirugo; T Jenkins; K K Kidd; A G Clark
Journal:  Am J Hum Genet       Date:  2000-09-13       Impact factor: 11.025

4.  Global haplotype diversity in the human insulin gene region.

Authors:  John D H Stead; Matthew E Hurles; Alec J Jeffreys
Journal:  Genome Res       Date:  2003-09       Impact factor: 9.043

5.  Differences between sliding semi-landmark methods in geometric morphometrics, with an application to human craniofacial and dental variation.

Authors:  S Ivan Perez; Valeria Bernal; Paula N Gonzalez
Journal:  J Anat       Date:  2006-06       Impact factor: 2.610

6.  Recent human effective population size estimated from linkage disequilibrium.

Authors:  Albert Tenesa; Pau Navarro; Ben J Hayes; David L Duffy; Geraldine M Clarke; Mike E Goddard; Peter M Visscher
Journal:  Genome Res       Date:  2007-03-09       Impact factor: 9.043

7.  High levels of Y-chromosome nucleotide diversity in the genus Pan.

Authors:  Anne C Stone; Robert C Griffiths; Stephen L Zegura; Michael F Hammer
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-26       Impact factor: 11.205

8.  Evidence for a possible Asian origin of YAP+ Y chromosomes.

Authors:  T K Altheide; M F Hammer
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

9.  Genetic traces of ancient demography.

Authors:  H C Harpending; M A Batzer; M Gurven; L B Jorde; A R Rogers; S T Sherry
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-17       Impact factor: 11.205

10.  Detecting interregionally diversifying natural selection on modern human cranial form by using matched molecular and morphometric data.

Authors:  Charles C Roseman
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-23       Impact factor: 11.205

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