Human Genetic Diversity: Lewontin's Fallacy
"Human Genetic Diversity: Lewontin's Fallacy" is a 2003 paper by A. W. F. Edwards. He criticises an argument first made by Richard Lewontin in his 1972 article "The Apportionment of Human Diversity", which argued that division of humanity into races is taxonomically invalid. Edwards' critique is discussed in a number of academic and popular science books, with varying degrees of support.
In the 1972 study "The Apportionment of Human Diversity", Richard Lewontin performed a fixation index (FST) statistical analysis using 17 markers, including blood group proteins, from individuals across classically defined "races" (Caucasian, African, Mongoloid, South Asian Aborigines, Amerinds, Oceanians, and, Australian Aborigines). He found that the majority of the total genetic variation between humans (i.e., of the 0.1% of DNA that varies between individuals), 85.4%, is found within populations, 8.3% of the variation is found between populations within a "race", and only 6.3% was found to account for the racial classification. Numerous later studies have confirmed his findings. Based on this analysis, Lewontin concluded, "Since such racial classification is now seen to be of virtually no genetic or taxonomic significance either, no justification can be offered for its continuance."
This argument has been cited as evidence that racial categories are biologically meaningless, and that behavioral differences between groups cannot have any genetic underpinnings. One example is the "Statement on 'Race'" published by the American Anthropological Association in 1998, which rejected the existence of races as unambiguous, clearly demarcated, biologically distinct groups.
Edwards argued that while Lewontin's statements on variability are correct when examining the frequency of different alleles (variants of a particular gene) at an individual locus (the location of a particular gene) between individuals, it is nonetheless possible to classify individuals into different racial groups with an accuracy that approaches 100 percent when one takes into account the frequency of the alleles at several loci at the same time. This happens because differences in the frequency of alleles at different loci are correlated across populations — the alleles that are more frequent in a population at two or more loci are correlated when we consider the two populations simultaneously. Or in other words, the frequency of the alleles tends to cluster differently for different populations.
In Edwards's words, "most of the information that distinguishes populations is hidden in the correlation structure of the data." These relationships can be extracted using commonly used ordination and cluster analysis techniques. Edwards argued that, even if the probability of misclassifying an individual based on the frequency of alleles at a single locus is as high as 30 percent (as Lewontin reported in 1972), the misclassification probability becomes close to zero if enough loci are studied.
Edwards's paper stated that the underlying logic was discussed in the early years of the 20th century. Edwards wrote that he and Luigi Luca Cavalli-Sforza had presented a contrasting analysis to Lewontin's, using very similar data, already at the 1963 International Congress of Genetics. Lewontin participated in the conference but did not refer to this in his later paper. Edwards argued that Lewontin used his analysis to attack human classification in science for social reasons.
Response to Edwards
Evolutionary biologist Richard Dawkins agreed with Edwards' view and summarized it as "However small the racial partition of the total variation may be, if such racial characteristics as there are highly correlate with other racial characteristics, they are by definition informative, and therefore of taxonomic significance." Dawkins also wrote of Lewontin that he is "known for the strength of his political convictions and his weakness for dragging them into science at every possible opportunity." Neven Sesardic has argued that, unbeknownst to Edwards, Jeffry B. Mitton already made the same argument about Lewontin's claim in two articles published in The American Naturalist in the late 1970s.
Philosophers Jonathan Kaplan and Rasmus Winther have argued that while Edwards's argument is correct it does not invalidate Lewontin's original argument, because racial groups being genetically distinct on average does not mean that racial groups are the most basic biological divisions of the world's population. Nor does it mean that races are not social constructs as is the prevailing view among anthropologists and social scientists, because the particular genetic differences that correspond to races only become salient when racial categories take on social importance. From this sociological perspective, Edwards and Lewontin are therefore both correct.
Similarly, biological anthropologist Jonathan Marks agrees with Edwards that correlations between geographical areas and genetics obviously exist in human populations, but goes on to note that "What is unclear is what this has to do with 'race' as that term has been used through much in the twentieth century - the mere fact that we can find groups to be different and can reliably allot people to them is trivial. Again, the point of the theory of race was to discover large clusters of people that are principally homogeneous within and heterogeneous between, contrasting groups. Lewontin's analysis shows that such groups do not exist in the human species, and Edwards' critique does not contradict that interpretation."
The view that while geographic clustering of biological traits does exist this does not lend biological validity to racial groups was proposed by several evolutionary anthropologists and geneticists prior to the publication of Edwards critique of Lewontin.
In the 2007 paper "Genetic Similarities Within and Between Human Populations", Witherspoon et al. attempt to answer the question, "How often is a pair of individuals from one population genetically more dissimilar than two individuals chosen from two different populations?". The answer depends on the number of polymorphisms used to define that dissimilarity, and the populations being compared. When they analysed three geographically distinct populations (European, African and East Asian) and measured genetic similarity over many thousands of loci, the answer to their question was "never". However, measuring similarity using smaller numbers of loci yielded substantial overlap between these populations. Rates of between-population similarity also increased when geographically intermediate and admixed populations were included in the analysis.
Witherspoon et al. conclude that, "Since an individual's geographic ancestry can often be inferred from his or her genetic makeup, knowledge of one's population of origin should allow some inferences about individual genotypes. To the extent that phenotypically important genetic variation resembles the variation studied here, we may extrapolate from genotypic to phenotypic patterns. [...] However, the typical frequencies of alleles responsible for common complex diseases remain unknown. The fact that, given enough genetic data, individuals can be correctly assigned to their populations of origin is compatible with the observation that most human genetic variation is found within populations, not between them. It is also compatible with our finding that, even when the most distinct populations are considered and hundreds of loci are used, individuals are frequently more similar to members of other populations than to members of their own population. Thus, caution should be used when using geographic or genetic ancestry to make inferences about individual phenotypes", and warn that, "A final complication arises when racial classifications are used as proxies for geographic ancestry. Although many concepts of race are correlated with geographic ancestry, the two are not interchangeable, and relying on racial classifications will reduce predictive power still further."
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- Lewontin, R. C. (1972). "The Apportionment of Human Diversity". Evolutionary Biology. pp. 381–398. doi:10.1007/978-1-4684-9063-3_14. ISBN 978-1-4684-9065-7.
- Made in "The Apportionment of Human Diversity" (1972)
- Dawkins, R. (2005). The Ancestor's Tale: A Pilgrimage to the Dawn of Evolution. with additional research by Y. Wong. New York: Houghton Mifflin Harcourt. pp. 406–407. ISBN 9780618619160.
- Ramachandran, S.; Tang, H.; Gutenkunst, R. N.; Bustamante, C. D. (2010). "Chapter 20: Genetics and Genomics of Human Population Structure". In Speicher, M. R. et al. Vogel and Motulsky's Human Genetics: Problems and Approaches. Heidelberg: Springer. p. 596. doi:10.1007/978-3-540-37654-5. ISBN 978-3-540-37653-8. Retrieved 29 October 2013. Lay summary (4 September 2010).
- Marks, J. (2010). "Ten Facts about Human Variation". In Muehlenbein, M. P. Human Evolutionary Biology. Cambridge University Press. p. 270. ISBN 9781139789004.
- American Anthropological Association (1998). "American Anthropological Association Statement on 'Race'".
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- Mitton, J. B. (1978). "Measurement of Differentiation: Reply to Lewontin, Powell, and Taylor". The American Naturalist 112 (988): 1142–1144. doi:10.1086/283359.
- Kaplan, J. M. (2011). "‘Race’: What Biology Can Tell Us about a Social Construct". Encyclopedia of Life Sciences. doi:10.1002/9780470015902.a0005857. ISBN 0470016175.
- Winther, Rasmus Grønfeldt (2011) ¿La cosificación genética de la 'raza'? Un análisis crítico in C López-Beltrán (ed.) Genes (&) Mestizos. Genómica y raza en la biomedicina mexicana. Ficticia editorial
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- Graves, Joseph L. (2003). The Emperor's New Clothes: Biological Theories of Race at the Millennium. Rutgers University Press. ISBN 0-8135-2847-X.
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