Posted: Aug 11, 2011 3:21 am
by Biowatch
mcgruff wrote:So what do we actually find?

  • human genetic diversity is unusually low for a primate species (as a result of recent near-extinction events)
  • you can pick any population at random anywhere on the planet and you will find almost all possible human variation within that group
  • more variation within a given population than between populations
  • multiple independent clines*
  • if you use enough markers (many thousands) you can identify which population an individual belongs to with very high accuracy (but not with smaller numbers of markers)
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1. Have you heard of the Lewontin Fallacy? Read Cambridge geneticist AWF Edwards' paper on it, or Steve Hsu's discussion here:

Further technical comment: you may have read the misleading statistic, spread by the intellectually dishonest Lewontin, that 85% percent of all human genetic variation occurs within groups and only 15% between groups. The statistic is true, but what is often falsely claimed is that this breakup of variances (larger within group than between group) prevents any meaningful genetic classification of populations. This false conclusion neglects the correlations in the genetic data that are revealed in a cluster analysis. See here for a simple example which shows that there can be dramatic group differences in phenotypes even if every version of every gene is found in two groups -- as long as the frequency or probability distributions are distinct. Sadly, understanding this point requires just enough mathematical ability that it has eluded all but a small number of experts.)


http://infoproc.blogspot.com/2008/01/no ... -race.html

2. What about the genetic diversity in comparison to other species which have sub-species or races?

Table 1. Comparative figures for the genetic diversity of humans and a variety of other large mammals (sampled across much or all of their range except as noted), based on autosomal microsatellites (He and Ho = expected and observed heterozygosity, respectively):


Species He Ho

Humans [18] -- 0.776
Humans [19] -- 0.70-0.76
Humans [20] -- 0.588-0.807
Chimpanzees [21] 0.78 0.73
Chimpanzees [22] -- 0.630
African buffalo [23] 0.759 0.729
Leopards [24] 0.36-0.80 --
Jaguars [25] 0.739 --
Polar bears [26] 0.68 --
Brown bears (N. America) [27] 0.26-0.76 0.30-0.79
Brown bears (Scandinavia) [28] 0.709 0.665
Canada lynx [29] -- 0.66
Bighorn sheep [30] 0.681 0.566
Coyote [31] 0.675 0.583
Gray wolf (N. America) [32] 0.620 0.528
Pumas [33] -- 0.52
Bonobos [34] 0.59 0.48
Dogs (42 breeds) [35] 0.616 0.401
African wild dogs [36] 0.643 --
Australian dingo [37] 0.47 0.42
Wolverines (N. America) [38] 0.42-0.68 --
Wolverines (Scandinavia) [39] -- 0.27-0.38
Elk (North America) [40] 0.26-0.53 --

Keeping the preceding caveats in mind, these are qualitative guidelines suggested by Sewall Wright for interpreting FST:

“The range 0 to 0.05 may be considered as indicating little genetic differentiation.
The range 0.05 to 0.15 indicates moderate genetic differentiation.
The range 0.15 to 0.25 indicates great genetic differentiation.
Values of FST above 0.25 indicate very great genetic differentiation.” [81]

Table 2.
Here are some comparative figures for humans and other species (again, sampled across most or all of their ranges except as noted), based on autosomal microsatellites:
Species FST
Gray wolves (North America) [82] 0.168
Pumas [83] 0.167 (mean pairwise)
Humans (14 populations) [84] 0.155 (AMOVA)
Asian dogs (11 breeds) [85] 0.154
European wildcats (Italy) [86] 0.13
Humans (44 populations) [87] 0.121 (AMOVA)
Coyotes (North America) [88] 0.107
Wolverines (North America) [89] 0.067 (mean pairwise)
Jaguars [90] 0.065
African buffalo [91] 0.059
Polar bears [92] 0.041 (mean pairwise)
Canada lynx [93] 0.033
Humpback whales [94] 0.026 (mean pairwise)

See data sources here http://www.goodrumj.com/RFaqHTML.html also, set out here by Woodley. http://tinyurl.com/4yoersb