There is minimal genetic variation across all humans. Being able to group certain traits doesn’t change the fact that differences among even family members are much larger than the differences between “races” and the variance within any “race” is much greater than the variance between “races”. There are multiple populations within Africa that are much more distantly related from each other that the supposed “races” are. The traits that separate these supposed “races” are basically irrelevant and have no correlation to genes that control other things.
A whopping of three questionable statements. We have the minimal genetic variation one, Lewontin's Fallacy and a claim that phylogenic groups and attached alleles are being arbitrarily linked to the term "race".
Human groups
are more genetically diverse than dogs are (if looking at heterozygosity then: humans 0.776, dogs 0.401). Also, differences between two seperate species of gorillas (G. berengi and G. Gorilla) are on the order of six times less than between african Bantu people and anglo-saxon british (drafted from
here and
here). I found Vincent Sarich's and Miele's book "
Race: The Reality of Human Differences" gave a good survey of the history of anthropology in this context, related genetics, the political and academic controversies, and the definitions of race. As he once noted: "
I am not aware of any other mammalian species where the constituent races are as strongly marked as they are in ours… except those few races heavily modified by recent human selection; in particular, dogs."
*
Genetic Structure, Self-Identified Race/Ethnicity, and Confounding in Case-Control Association Studies:
3,636 subjects of varying race/ethnicity, only 5 (0.14%) showed genetic cluster membership different from their self-identified race/ethnicity. On the other hand, we detected only modest genetic differentiation between different current geographic locales within each race/ethnicity group. Thus, ancient geographic ancestry, which is highly correlated with self-identified race/ethnicity—as opposed to current residence—is the major determinant of genetic structure in the U.S. population.
*
Let's celebrate human genetic diversity: [Ebenstein, Lanny. Lahn, Bruce. [
Nature, 8 October 2009]
The current moral position is a sort of 'biological egalitarianism'. This dominant position emerged in recent decades largely to correct grave historical injustices, including genocide, that were committed with the support of pseudoscientific understandings of group diversity. The racial-hygiene theory promoted by German geneticists Fritz Lenz, Eugene Fischer and others during the Nazi era is one notorious example of such pseudoscience. Biological egalitarianism is the view that no or almost no meaningful genetically based biological differences exist among human groups, with the exception of a few superficial traits such as skin colour. Proponents of this view seem to hope that, by promoting biological sameness, discrimination against groups or individuals will become groundless.
...
Genetic diversity is the differences in DNA sequence among members of a species. It is present in all species owing to the interplay of mutation, genetic drift, selection and population structure. When a species is reproductively isolated into multiple groups by geography or other means, the groups differentiate over time in their average genetic make-up.
Anatomically modern humans first appeared in eastern Africa about 200,000 years ago. Some members migrated out of Africa by 50,000 years ago to populate Asia, Australia, Europe and eventually the Americas. During this period, geographic barriers separated humanity into several major groups, largely along continental lines, which greatly reduced gene flow among them. Geographic and cultural barriers also existed within major groups, although to lesser degrees.
This history of human demography, along with selection, has resulted in complex patterns of genetic diversity. The basic unit of this diversity is polymorphisms — specific sites in the genome that exist in multiple variant forms (or alleles). Many polymorphisms involve just one or a few nucleotides, but some may involve large segments of genetic material. The presence of polymorphisms leads to genetic diversity at the individual level such that no two people's DNA is the same, except identical twins. The alleles of some polymorphisms are also found in significantly different frequencies among geographic groups. An extreme example is the pigmentation gene SLC24A5. An allele of SLC24A5 that contributes to light pigmentation is present in almost all Europeans but is nearly absent in east Asians and Africans.
Given these geographically differentiated polymorphisms, it is possible to group humans on the basis of their genetic make-up. Such grouping largely confirms historical separation of global populations by geography. Indeed, a person's major geographic group identity can be assigned with near certainty on the basis of his or her DNA alone (now an accepted practice in forensics). There is growing evidence that some of the geographically differentiated polymorphisms are functional, meaning that they can lead to different biological outcomes (just how many is the subject of ongoing research). These polymorphisms can affect traits such as pigmentation, dietary adaptation and pathogen resistance (where evidence is rather convincing), and metabolism, physical development and brain biology (where evidence is more preliminary).
Quite a different story from the one you're telling
lomiller.
For a rough yet clear comparison of the striking similarities between a couple of, allegedly, inconsistent groupings, Carelton Coon's prime-race category were at one time Austroloid, Congoloid, Capoid, Mongoloid and Caucasoid (of which there were sub-branches). Then, the zero-race system used by Brace (calling it geographic clusters instead) had eight of such 'sub-branches'; Australo-Melanesia (comparable to Coon's Austroloid), Africa (Congoloid, Capoid), Amerind-Jomon Pacific-Asia-Eskimo (Mongoloid), India-Europe (Caucasoid). Both involve a racial (sub-specie) taxon, where the only difference is (not the variables included) are the
main structuring of groups.
Ironically (well, not really), Sforza's groupings are notably similar to Carleton Coon's racial groupings is interesting, especially as the former is supposed/argued to be somewhat of the 'dean' on the human genome and its viable "biogeographical" groups. I do not understand the utter denial by some here, still to this day (I mean it's not the 70's is it?).
These are basic hereditary breeds within a species whose geographical, genetic as well as historical isolations can account for their genetic distances inbetween each other. In a much simpler, conventional way, we do the same with dog breeds et al. As Templeton wrote in
'Human races: a genetic and evolutionary perspective':
subspecies (race) is a distinct evolutionary lineage within a species. This definition requires that a subspecies be genetically differentiated due to barriers to genetic exchange that have persisted for long periods of time; that is, the subspecies must have historical continuity in addition to current genetic differentiation
People react toward the term 'race', usually because of knee-jerk association with "bad" things and political musings thereof of course. Rationalizing this, the argument is that it isn't precise or defined enough to be valid, all while not realising/recognising that by the same token we could then throw out most of our classifications of the animal kingdom right out the window. Still, it isn't even necessary to use the r-word. Ashley Montague (allthough arguing on behalf of extreme enviromentalism as opposed to nature) termed it ethniticity, making it appliable even more six ways from sunday... all while the same darn observations are made empirically, showing us that nature will come out (as Feynman put it) they way it is no matter what we call it or what our expectations are. This is why, for example, Coon's own groupings of human beings (many times his added musings and elaborations were beyond reason) matches up quite well with Sforsa's volumnous work and studies on the human genome project.