Recent from talks
Nothing was collected or created yet.
Race (human categorization)
View on Wikipedia
This article should specify the language of its non-English content using {{lang}} or {{langx}}, {{transliteration}} for transliterated languages, and {{IPA}} for phonetic transcriptions, with an appropriate ISO 639 code. Wikipedia's multilingual support templates may also be used. (July 2025) |
| Race |
|---|
| History |
| Society |
| Race and... |
| By location |
| Related topics |
| Part of a series on |
| Anthropology |
|---|
Race is a categorization of humans based on shared physical or social qualities into groups generally viewed as distinct within a given society.[1] The term came into common usage during the 16th century, when it was used to refer to groups of various kinds, including those characterized by close kinship relations.[2] By the 17th century, the term began to refer to physical (phenotypical) traits, and then later to national affiliations. Modern science regards race as a social construct, an identity which is assigned based on rules made by society.[3][4][5] While partly based on physical similarities within groups, race does not have an inherent physical or biological meaning.[1][6][7] The concept of race is foundational to racism, the belief that humans can be divided based on the superiority of one race over another.
Social conceptions and groupings of races have varied over time, often involving folk taxonomies that define essential types of individuals based on perceived traits.[8] Modern scientists consider such biological essentialism obsolete,[9] and generally discourage racial explanations for collective differentiation in both physical and behavioral traits.[10][11][12][13][14]
Even though there is a broad scientific agreement that essentialist and typological conceptions of race are untenable,[15][16][17][18][19][20] scientists around the world continue to conceptualize race in widely differing ways.[21] While some researchers continue to use the concept of race to make distinctions among fuzzy sets of traits or observable differences in behavior, others in the scientific community suggest that the idea of race is inherently naive[10] or simplistic.[22] Still others argue that, among humans, race has no taxonomic significance because all living humans belong to the same subspecies, Homo sapiens sapiens.[23][24]
Since the second half of the 20th century, race has been associated with discredited theories of scientific racism and has become increasingly seen as an essentially pseudoscientific system of classification. Although still used in general contexts, race has often been replaced by less ambiguous and/or loaded terms: populations, people(s), ethnic groups, or communities, depending on context.[25][26] Its use in genetics was formally renounced by the U.S. National Academies of Sciences, Engineering, and Medicine in 2023.[27]
Defining race
[edit]Modern scholarship views racial categories as socially constructed, that is, race is not intrinsic to human beings but rather an identity created, often by socially dominant groups, to establish meaning in a social context. Different cultures define different racial groups, often focused on the largest groups of social relevance, and these definitions can change over time.
Historical race concepts have included a wide variety of schemes to divide local or worldwide populations into races and sub-races. Across the world, different organizations and societies choose to disambiguate race to different extents:
- In South Africa, the Population Registration Act, 1950 recognized only White, Black, and Coloured, with Indians added later.[28]
- The government of Myanmar recognizes eight "major national ethnic races".
- The Brazilian census classifies people into brancos (Whites), pardos (multiracial), pretos (Blacks), amarelos (Asians), and indigenous (see Race and ethnicity in Brazil), though many people use different terms to identify themselves.
- Legal definitions of whiteness in the United States used before the civil rights movement were often challenged for specific groups.
- Furthermore, the United States Census Bureau proposed but then withdrew plans to add a new category to classify Middle Eastern and North African peoples in the 2020 U.S. census, due to a dispute over whether this classification should be considered a white ethnicity or a separate race.[29]
The establishment of racial boundaries often involves the subjugation of groups defined as racially inferior, as in the one-drop rule used in the 19th-century United States to exclude those with any amount of African ancestry from the dominant racial grouping, defined as "white".[1] Such racial identities reflect the cultural attitudes of imperial powers dominant during the age of European colonial expansion.[6] This view rejects the notion that race is biologically defined.[30][31][32][33]
According to geneticist David Reich, "while race may be a social construct, differences in genetic ancestry that happen to correlate to many of today's racial constructs are real".[34] In response to Reich, a group of 67 scientists from a broad range of disciplines wrote that his concept of race was "flawed" as "the meaning and significance of the groups is produced through social interventions".[35]
Although commonalities in physical traits such as facial features, skin color, and hair texture comprise part of the race concept, this linkage is a social distinction rather than an inherently biological one.[1] Other dimensions of racial groupings include shared history, traditions, and language. For instance, African-American English is a dialect of English spoken by many African Americans, especially in areas of the United States where racial segregation formerly existed. Furthermore, many people often will self-identify as members of a race for political reasons.[1]
When people define and talk about a particular conception of race, they create a social reality through which social categorization is achieved.[36] In this sense, races are said to be social constructs.[37] These constructs develop within various legal, economic, and sociopolitical contexts, and may be the effect, rather than the cause, of major social situations.[clarify][38] While race is understood to be a social construct by many, most scholars agree that race has real material effects in the lives of people through institutionalized practices of preference and discrimination.[39]
Socioeconomic factors, in combination with early but enduring views of race, have led to considerable suffering within disadvantaged racial groups.[40] Racial discrimination often coincides with racist mindsets, whereby the individuals and ideologies of one group come to perceive the members of an outgroup as both racially defined and morally inferior.[41] As a result, racial groups possessing relatively little power often find themselves excluded or oppressed, while hegemonic individuals and institutions are charged with holding racist attitudes.[42] Racism has led to many instances of tragedy, including slavery and genocide.[43]
In some countries, law enforcement uses race to profile suspects. This use of racial categories is frequently criticized for perpetuating an outmoded understanding of human biological variation, and promoting stereotypes. Because in some societies racial groupings correspond closely with patterns of social stratification, for social scientists studying social inequality, race can be a significant variable. As sociological factors, racial categories may in part reflect subjective attributions, self-identities, and social institutions.[44][45]
Scholars continue to debate the degrees to which racial categories are biologically warranted and socially constructed.[46] For example, in 2008, John Hartigan Jr. argued for a view of race that focused primarily on culture, but which does not ignore the potential relevance of biology or genetics.[47] Accordingly, the racial paradigms employed in different disciplines vary in their emphasis on biological reduction as contrasted with societal construction.
In the social sciences, theoretical frameworks such as racial formation theory and critical race theory investigate implications of race as social construction by exploring how the images, ideas and assumptions of race are expressed in everyday life. A large body of scholarship has traced the relationships between the historical and social production of race in legal and criminal language, and their effects on the policing and disproportionate incarceration of certain groups.
Historical origins of racial classification
[edit]
- Mongoloid race, shown in yellow and orange tones
- Caucasoid race, in light and medium grayish spring green-cyan tones
- Negroid race, in brown tones
- Dravidians and Sinhalese, in olive green and their classification is described as uncertain

Groups of humans have always identified themselves as distinct from neighboring groups, but such differences have not always been understood to be natural, immutable and global. These features are the distinguishing features of how the concept of race is used today. In this way the idea of race as we understand it today came about during the historical process of exploration and conquest which brought Europeans into contact with groups from different continents, and of the ideology of classification and typology found in the natural sciences.[48] The term race was often used in a general biological taxonomic sense,[25] starting from the 19th century, to denote genetically differentiated human populations defined by phenotype.[49][50]
The modern concept of race emerged as a product of the colonial enterprises of European powers from the 16th to 18th centuries which identified race in terms of skin color and physical differences. Author Rebecca F. Kennedy argues that the Greeks and Romans would have found such concepts confusing in relation to their own systems of classification.[51] According to Bancel et al., the epistemological moment where the modern concept of race was invented and rationalized lies somewhere between 1730 and 1790.[52]
Colonialism
[edit]According to Smedley and Marks the European concept of "race", along with many of the ideas now associated with the term, arose at the time of the Scientific Revolution, which introduced and privileged the study of natural kinds, and the age of European imperialism and colonization which established political relations between Europeans and peoples with distinct cultural and political traditions.[48][53] As Europeans encountered people from different parts of the world, they speculated about the physical, social, and cultural differences among various human groups. The rise of the Atlantic slave trade, which gradually displaced an earlier trade in slaves from throughout the world, created a further incentive to categorize human groups in order to justify the subordination of African slaves.[54]
Drawing on sources from classical antiquity and upon their own internal interactions – for example, the hostility between the English and Irish powerfully influenced early European thinking about the differences between people[55] – Europeans began to sort themselves and others into groups based on physical appearance, and to attribute to individuals belonging to these groups behaviors and capacities which were claimed to be deeply ingrained. A set of folk beliefs took hold that linked inherited physical differences between groups to inherited intellectual, behavioral, and moral qualities.[56] Similar ideas can be found in other cultures,[57] for example in China, where a concept often translated as "race" was associated with supposed common descent from the Yellow Emperor, and used to stress the unity of ethnic groups in China. Brutal conflicts between ethnic groups have existed throughout history and across the world.[58]
Early taxonomic models
[edit]The first post-Graeco-Roman published classification of humans into distinct races seems to be François Bernier's Nouvelle division de la terre par les différents espèces ou races qui l'habitent ("New division of Earth by the different species or races which inhabit it"), published in 1684.[59] In the 18th century the differences among human groups became a focus of scientific investigation. But the scientific classification of phenotypic variation was frequently coupled with racist ideas about innate predispositions of different groups, always attributing the most desirable features to the White, European race and arranging the other races along a continuum of progressively undesirable attributes. The 1735 classification of Carl Linnaeus, inventor of zoological taxonomy, divided the human species Homo sapiens into continental varieties of europaeus, asiaticus, americanus, and afer, each associated with a different humour: sanguine, melancholic, choleric, and phlegmatic, respectively.[60][61] Homo sapiens europaeus was described as active, acute, and adventurous, whereas Homo sapiens afer was said to be crafty, lazy, and careless.[62]
The 1775 treatise "The Natural Varieties of Mankind", by Johann Friedrich Blumenbach proposed five major divisions: the Caucasoid race, the Mongoloid race, the Ethiopian race (later termed Negroid), the American Indian race, and the Malayan race, but he did not propose any hierarchy among the races.[62] Blumenbach also noted the graded transition in appearances from one group to adjacent groups and suggested that "one variety of mankind does so sensibly pass into the other, that you cannot mark out the limits between them".[63]
From the 17th through 19th centuries, the merging of folk beliefs about group differences with scientific explanations of those differences produced what Smedley has called an "ideology of race".[53] According to this ideology, races are primordial, natural, enduring and distinct. It was further argued that some groups may be the result of mixture between formerly distinct populations, but that careful study could distinguish the ancestral races that had combined to produce admixed groups.[58] Subsequent influential classifications by Georges Buffon, Petrus Camper and Christoph Meiners all classified "Negros" as inferior to Europeans.[62] In the United States the racial theories of Thomas Jefferson were influential. He saw Africans as inferior to Whites especially in regards to their intellect, and imbued with unnatural sexual appetites, but described Native Americans as equals to whites.[64]
Polygenism vs monogenism
[edit]In the last two decades of the 18th century, the theory of polygenism, the belief that different races had evolved separately in each continent and shared no common ancestor,[65] was advocated in England by historian Edward Long and anatomist Charles White, in Germany by ethnographers Christoph Meiners and Georg Forster, and in France by Julien-Joseph Virey. In the US, Samuel George Morton, Josiah Nott and Louis Agassiz promoted this theory in the mid-19th century. Polygenism was popular and most widespread in the 19th century, culminating in the founding of the Anthropological Society of London (1863), which, during the period of the American Civil War, broke away from the Ethnological Society of London and its monogenic stance, their underlined difference lying, relevantly, in the so-called "Negro question": a substantial racist view by the former,[66] and a more liberal view on race by the latter.[67]
Modern scholarship
[edit]Models of human evolution
[edit]Today, all humans are classified as belonging to the species Homo sapiens. However, this is not the first species of homininae: the first species of the genus Homo, Homo habilis, evolved in East Africa at least 2 million years ago, and members of this species populated different parts of Africa in a relatively short time. Homo erectus evolved more than 1.8 million years ago and, by 1.5 million years ago, had spread throughout Europe and Asia. Virtually all physical anthropologists agree that Archaic Homo sapiens (A group including the possible species H. heidelbergensis, H. rhodesiensis, and H. neanderthalensis) evolved out of African H. erectus (sensu lato) or H. ergaster.[68][69] Anthropologists support the idea that anatomically modern humans (Homo sapiens) evolved in North or East Africa from an archaic human species such as H. heidelbergensis and then migrated out of Africa, mixing with and replacing H. heidelbergensis and H. neanderthalensis populations throughout Europe and Asia, and H. rhodesiensis populations in Sub-Saharan Africa (a combination of the Out of Africa and Multiregional models).[70][verification needed]
Biological classification
[edit]In the early 20th century, many anthropologists taught that race was an entirely biological phenomenon and that this was core to a person's behavior and identity, a position commonly called racial essentialism.[71] This, coupled with the belief that linguistic, cultural, and social groups fundamentally existed along racial lines, formed the basis of what is now called scientific racism.[72] After the Nazi eugenics program, along with the rise of anti-colonial movements, racial essentialism lost widespread popularity.[73] New studies of culture and the fledgling field of population genetics undermined the scientific standing of racial essentialism, leading race anthropologists to revise their conclusions about the sources of phenotypic variation.[71] A significant number of modern anthropologists and biologists in the West came to view race as an invalid genetic or biological designation.[74]
The first to challenge the concept of race on empirical grounds were the anthropologists Franz Boas, who provided evidence of phenotypic plasticity due to environmental factors,[75] and Ashley Montagu, who relied on evidence from genetics.[76] E. O. Wilson then challenged the concept from the perspective of general animal systematics and further rejected the claim that "races" were equivalent to "subspecies".[77]
Human genetic variation is predominantly within races, continuous, and complex in structure, which is inconsistent with the concept of genetic human races.[78] According to the biological anthropologist Jonathan Marks,[48]
By the 1970s, it had become clear that (1) most human differences were cultural; (2) what was not cultural was principally polymorphic – that is to say, found in diverse groups of people at different frequencies; (3) what was not cultural or polymorphic was principally clinal – that is to say, gradually variable over geography; and (4) what was left – the component of human diversity that was not cultural, polymorphic, or clinal – was very small.
A consensus consequently developed among anthropologists and geneticists that race as the previous generation had known it – as largely discrete, geographically distinct, gene pools – did not exist.
Subspecies
[edit]The term race in biology is used with caution because it can be ambiguous. Generally, when it is used it is effectively a synonym of subspecies.[79] (For animals, the only taxonomic unit below the species level is usually the subspecies;[80] there are narrower infraspecific ranks in botany, and race does not correspond directly with any of them.) Traditionally, subspecies are seen as geographically isolated and genetically differentiated populations.[81] Studies of human genetic variation show that human populations are not geographically isolated,[82] and their genetic differences are far smaller than those among comparable subspecies.[83]
In 1978, Sewall Wright suggested that human populations that have long inhabited separated parts of the world should generally be considered different subspecies by the criterion that most individuals of such populations can be allocated correctly by inspection. Wright argued: "It does not require a trained anthropologist to classify an array of Englishmen, West Africans, and Chinese with 100% accuracy by features, skin color, and type of hair despite so much variability within each of these groups that every individual can easily be distinguished from every other."[84] In practice, subspecies are commonly identified based on easily observable physical traits, but the variations in these traits among members of a species do not always hold evolutionary significance, resulting in a decreased acceptance of this classification method among evolutionary biologists.[85] Likewise, this typological approach to race is generally regarded as discredited by biologists and anthropologists.[86][17]
Ancestrally differentiated populations (clades)
[edit]In 2000, philosopher Robin Andreasen proposed that cladistics might be used to categorize human races biologically and that races can be both biologically real and socially constructed.[87] Andreasen cited tree diagrams of relative genetic distances among populations published by Luigi Cavalli-Sforza as the basis for a phylogenetic tree of human races (p. 661). Biological anthropologist Jonathan Marks (2008) responded by arguing that Andreasen had misinterpreted the genetic literature: "These trees are phenetic (based on similarity), rather than cladistic (based on monophyletic descent, that is from a series of unique ancestors)."[88] Evolutionary biologist Alan Templeton (2013) argued that multiple lines of evidence falsify the idea of a phylogenetic tree structure to human genetic diversity and confirm the presence of gene flow among populations.[33] Marks, Templeton, and Cavalli-Sforza all conclude that genetics does not provide evidence of human races.[33][89]
Previously, anthropologists Lieberman and Jackson (1995) had also critiqued the use of cladistics to support concepts of race. They argued that "the molecular and biochemical proponents of this model explicitly use racial categories in their initial grouping of samples". For example, the large and highly diverse macroethnic groups of East Indians, North Africans, and Europeans are presumptively grouped as Caucasians prior to the analysis of their DNA variation. They argued that this a priori grouping limits and skews interpretations, obscures other lineage relationships, deemphasizes the impact of more immediate clinal environmental factors on genomic diversity, and can cloud our understanding of the true patterns of affinity.[90]
In 2015, Keith Hunley, Graciela Cabana, and Jeffrey Long analyzed the Human Genome Diversity Project sample of 1,037 individuals in 52 populations,[91] finding that diversity among non-African populations is the result of a serial founder effect process, with non-African populations as a whole nested among African populations, that "some African populations are equally related to other African populations and to non-African populations", and that "outside of Africa, regional groupings of populations are nested inside one another, and many of them are not monophyletic".[91] Earlier research had also suggested that there has always been considerable gene flow between human populations, meaning that human population groups are not monophyletic.[81] Rachel Caspari has argued that since no groups currently regarded as races are monophyletic, by definition, none of these groups can be clades.[92]
Clines
[edit]One crucial innovation in reconceptualizing genotypic and phenotypic variation was the anthropologist C. Loring Brace's observation that such variations, insofar as they are affected by natural selection, slow migration, or genetic drift, are distributed along geographic gradations or clines.[93] For example, with respect to skin color in Europe and Africa, Brace writes:[94]
To this day, skin color grades by imperceptible means from Europe southward around the eastern end of the Mediterranean and up the Nile into Africa. From one end of this range to the other, there is no hint of a skin color boundary, and yet the spectrum runs from the lightest in the world at the northern edge to as dark as it is possible for humans to be at the equator.
This is partly due to isolation by distance, a point that called attention to a problem common to phenotype-based descriptions of races (e.g., those based on hair texture and skin color): they ignore a host of other similarities and differences (for example, blood type) that do not correlate highly with the markers for race. Thus, anthropologist Frank Livingstone concluded that, since clines cross racial boundaries, "there are no races, only clines."[95]
In a response to Livingstone, Theodore Dobzhansky argued that when talking about race, one must be attentive to how the term is being used: "I agree with Dr. Livingstone that if races have to be 'discrete units', then there are no races, and if 'race' is used as an 'explanation' of the human variability, rather than vice versa, then the explanation is invalid." He further argued that one could use the term race if one distinguished between "race differences" and "the race concept". The former refers to any distinction in gene frequencies between populations; the latter is "a matter of judgment". He further observed that even when there is clinal variation: "Race differences are objectively ascertainable biological phenomena ... but it does not follow that racially distinct populations must be given racial (or subspecific) labels."[95] In short, Livingstone and Dobzhansky agree that there are genetic differences among human beings; they also agree that the use of the race concept to classify people, and how the race concept is used, is a matter of social convention. They differ on whether the race concept remains a meaningful and useful social convention.
In 1964, the biologists Paul Ehrlich and Holm pointed out cases where two or more clines are distributed discordantly – for example, melanin is distributed in a decreasing pattern from the equator north and south; frequencies for the haplotype for beta-S hemoglobin, on the other hand, radiate out of specific geographical points in Africa.[96] As the anthropologists Leonard Lieberman and Fatimah Linda Jackson observed, "Discordant patterns of heterogeneity falsify any description of a population as if it were genotypically or even phenotypically homogeneous".[90]
Patterns such as those seen in human physical and genetic variation as described above, have led to the consequence that the number and geographic location of any described races is highly dependent on the importance attributed to, and quantity of, the traits considered. A skin-lightening mutation, estimated to have occurred 20,000 to 50,000 years ago, partially accounts for the appearance of light skin in people who migrated out of Africa northward into what is now Europe. East Asians owe their relatively light skin to different mutations.[97] On the other hand, the greater the number of traits (or alleles) considered, the more subdivisions of humanity are detected, since traits and gene frequencies do not always correspond to the same geographical location. Or as Ossorio & Duster (2005) put it:
Anthropologists long ago discovered that humans' physical traits vary gradually, with groups that are close geographic neighbors being more similar than groups that are geographically separated. This pattern of variation, known as clinal variation, is also observed for many alleles that vary from one human group to another. Another observation is that traits or alleles that vary from one group to another do not vary at the same rate. This pattern is referred to as nonconcordant variation. Because the variation of physical traits is clinal and nonconcordant, anthropologists of the late 19th and early 20th centuries discovered that the more traits and the more human groups they measured, the fewer discrete differences they observed among races and the more categories they had to create to classify human beings. The number of races observed expanded to the 1930s and 1950s, and eventually anthropologists concluded that there were no discrete races.[98] Twentieth and 21st century biomedical researchers have discovered this same feature when evaluating human variation at the level of alleles and allele frequencies. Nature has not created four or five distinct, nonoverlapping genetic groups of people.
Genetically differentiated populations
[edit]Another way to look at differences between populations is to measure genetic differences rather than physical differences between groups. The mid-20th-century anthropologist William C. Boyd defined race as: "A population which differs significantly from other populations in regard to the frequency of one or more of the genes it possesses. It is an arbitrary matter which, and how many, gene loci we choose to consider as a significant 'constellation'".[99] Leonard Lieberman and Rodney Kirk have pointed out that "the paramount weakness of this statement is that if one gene can distinguish races then the number of races is as numerous as the number of human couples reproducing".[100] Moreover, the anthropologist Stephen Molnar has suggested that the discordance of clines inevitably results in a multiplication of races that renders the concept itself useless.[101] The Human Genome Project states "People who have lived in the same geographic region for many generations may have some alleles in common, but no allele will be found in all members of one population and in no members of any other."[102] Massimo Pigliucci and Jonathan Kaplan argue that human races do exist, and that they correspond to the genetic classification of ecotypes, but that real human races do not correspond very much, if at all, to folk racial categories.[103] In contrast, Walsh & Yun reviewed the literature in 2011 and reported: "Genetic studies using very few chromosomal loci find that genetic polymorphisms divide human populations into clusters with almost 100 percent accuracy and that they correspond to the traditional anthropological categories."[104]
Some biologists argue that racial categories correlate with biological traits (e.g. phenotype), and that certain genetic markers have varying frequencies among human populations, some of which correspond more or less to traditional racial groupings.[105]
Distribution of genetic variation
[edit]The distribution of genetic variants within and among human populations are impossible to describe succinctly because of the difficulty of defining a population, the clinal nature of variation, and heterogeneity across the genome (Long and Kittles 2003). In general, however, an average of 85% of statistical genetic variation exists within local populations, ≈7% is between local populations within the same continent, and ≈8% of variation occurs between large groups living on different continents.[106][107] The recent African origin theory for humans would predict that in Africa there exists a great deal more diversity than elsewhere and that diversity should decrease the further from Africa a population is sampled. Hence, the 85% average figure is misleading: Long and Kittles find that rather than 85% of human genetic diversity existing in all human populations, about 100% of human diversity exists in a single African population, whereas only about 60% of human genetic diversity exists in the least diverse population they analyzed (the Surui, a population derived from New Guinea).[108] Statistical analysis that takes this difference into account confirms previous findings that "Western-based racial classifications have no taxonomic significance".[91]
Cluster analysis
[edit]A 2002 study of random biallelic genetic loci found little to no evidence that humans were divided into distinct biological groups.[109]
In his 2003 paper, "Human Genetic Diversity: Lewontin's Fallacy", A. W. F. Edwards argued that rather than using a locus-by-locus analysis of variation to derive taxonomy, it is possible to construct a human classification system based on characteristic genetic patterns, or clusters inferred from multilocus genetic data.[110][111] Geographically based human studies since have shown that such genetic clusters can be derived from analyzing of a large number of loci which can assort individuals sampled into groups analogous to traditional continental racial groups.[112][113] Joanna Mountain and Neil Risch cautioned that while genetic clusters may one day be shown to correspond to phenotypic variations between groups, such assumptions were premature as the relationship between genes and complex traits remains poorly understood.[114] However, Risch denied such limitations render the analysis useless: "Perhaps just using someone's actual birth year is not a very good way of measuring age. Does that mean we should throw it out? ... Any category you come up with is going to be imperfect, but that doesn't preclude you from using it or the fact that it has utility."[115]
Early human genetic cluster analysis studies were conducted with samples taken from ancestral population groups living at extreme geographic distances from each other. It was thought that such large geographic distances would maximize the genetic variation between the groups sampled in the analysis, and thus maximize the probability of finding cluster patterns unique to each group. In light of the historically recent acceleration of human migration (and correspondingly, human gene flow) on a global scale, further studies were conducted to judge the degree to which genetic cluster analysis can pattern ancestrally identified groups as well as geographically separated groups. One such study looked at a large multiethnic population in the United States, and "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."[113]
Witherspoon et al. (2007) have argued that even when individuals can be reliably assigned to specific population groups, it may still be possible for two randomly chosen individuals from different populations/clusters to be more similar to each other than to a randomly chosen member of their own cluster. They found that many thousands of genetic markers had to be used in order for the answer to the question "How often is a pair of individuals from one population genetically more dissimilar than two individuals chosen from two different populations?" to be "never". This assumed three population groups separated by large geographic ranges (European, African and East Asian). The entire world population is much more complex and studying an increasing number of groups would require an increasing number of markers for the same answer. The authors conclude that "caution should be used when using geographic or genetic ancestry to make inferences about individual phenotypes".[116] Witherspoon, et al. concluded: "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."[116]
Anthropologists such as C. Loring Brace,[117] the philosophers Jonathan Kaplan and Rasmus Winther,[118][119][120][121] and the geneticist Joseph Graves,[122] have argued that the cluster structure of genetic data is dependent on the initial hypotheses of the researcher and the influence of these hypotheses on the choice of populations to sample. When one samples continental groups, the clusters become continental, but if one had chosen other sampling patterns, the clustering would be different. Weiss and Fullerton have noted that if one sampled only Icelanders, Mayans and Maoris, three distinct clusters would form and all other populations could be described as being clinally composed of admixtures of Maori, Icelandic and Mayan genetic materials.[123] Kaplan and Winther therefore argue that, seen in this way, both Lewontin and Edwards are right in their arguments. They conclude that while racial groups are characterized by different allele frequencies, this does not mean that racial classification is a natural taxonomy of the human species, because multiple other genetic patterns can be found in human populations that crosscut racial distinctions. Moreover, the genomic data underdetermines whether one wishes to see subdivisions (i.e., splitters) or a continuum (i.e., lumpers). Under Kaplan and Winther's view, racial groupings are objective social constructions (see Mills 1998[124]) that have conventional biological reality only insofar as the categories are chosen and constructed for pragmatic scientific reasons. In earlier work, Winther had identified "diversity partitioning" and "clustering analysis" as two separate methodologies, with distinct questions, assumptions, and protocols. Each is also associated with opposing ontological consequences vis-a-vis the metaphysics of race.[120] Philosopher Lisa Gannett has argued that biogeographical ancestry, a concept devised by Mark Shriver and Tony Frudakis, is not an objective measure of the biological aspects of race as Shriver and Frudakis claim it is. She argues that it is actually just a "local category shaped by the U.S. context of its production, especially the forensic aim of being able to predict the race or ethnicity of an unknown suspect based on DNA found at the crime scene".[125]
Clines and clusters in genetic variation
[edit]Recent studies of human genetic clustering have included a debate over how genetic variation is organized, with clusters and clines as the main possible orderings. Serre & Pääbo (2004) argued for smooth, clinal genetic variation in ancestral populations even in regions previously considered racially homogeneous, with the apparent gaps turning out to be artifacts of sampling techniques. Rosenberg et al. (2005) disputed this and offered an analysis of the Human Genetic Diversity Panel showing that there were small discontinuities in the smooth genetic variation for ancestral populations at the location of geographic barriers such as the Sahara, the Oceans, and the Himalayas. Nonetheless, Rosenberg et al. (2005) stated that their findings "should not be taken as evidence of our support of any particular concept of biological race ... Genetic differences among human populations derive mainly from gradations in allele frequencies rather than from distinctive 'diagnostic' genotypes." Using a sample of 40 populations distributed roughly evenly across the Earth's land surface, Xing & et al. (2010, p. 208) found that "genetic diversity is distributed in a more clinal pattern when more geographically intermediate populations are sampled".
Guido Barbujani has written that human genetic variation is generally distributed continuously in gradients across much of Earth, and that there is no evidence that genetic boundaries between human populations exist as would be necessary for human races to exist.[126]
Over time, human genetic variation has formed a nested structure that is inconsistent with the concept of races that have evolved independently of one another.[127]
Social constructions
[edit]As anthropologists and other evolutionary scientists have shifted away from the language of race to the term population to talk about genetic differences, historians, cultural anthropologists and other social scientists re-conceptualized the term "race" as a cultural category or identity, i.e., a way among many possible ways in which a society chooses to divide its members into categories.
Many social scientists have replaced the word race with the word "ethnicity" to refer to self-identifying groups based on beliefs concerning shared culture, ancestry and history. Alongside empirical and conceptual problems with "race", following the Second World War, evolutionary and social scientists were acutely aware of how beliefs about race had been used to justify discrimination, apartheid, slavery, and genocide. This questioning gained momentum in the 1960s during the civil rights movement in the United States and the emergence of numerous anti-colonial movements worldwide. They thus came to believe that race itself is a social construct, a concept that was believed to correspond to an objective reality but which was believed in because of its social functions.[128]
Craig Venter and Francis Collins of the National Institute of Health jointly made the announcement of the mapping of the human genome in 2000. Upon examining the data from the genome mapping, Venter realized that although the genetic variation within the human species is on the order of 1–3% (instead of the previously assumed 1%), the types of variations do not support the notion of genetically defined races. Venter said, "Race is a social concept. It's not a scientific one. There are no bright lines (that would stand out), if we could compare all the sequenced genomes of everyone on the planet. ... When we try to apply science to try to sort out these social differences, it all falls apart."[129]
Anthropologist Stephan Palmié has argued that race "is not a thing but a social relation";[130] or, in the words of Katya Gibel Mevorach, "a metonym", "a human invention whose criteria for differentiation are neither universal nor fixed but have always been used to manage difference".[131] As such, the use of the term "race" itself must be analyzed. Moreover, they argue that biology will not explain why or how people use the idea of race; only history and social relationships will.
Imani Perry has argued that race "is produced by social arrangements and political decision making",[132] and that "race is something that happens, rather than something that is. It is dynamic, but it holds no objective truth."[133] Similarly, in Racial Culture: A Critique (2005), Richard T. Ford argued that while "there is no necessary correspondence between the ascribed identity of race and one's culture or personal sense of self" and "group difference is not intrinsic to members of social groups but rather contingent o[n] the social practices of group identification", the social practices of identity politics may coerce individuals into the "compulsory" enactment of "prewritten racial scripts".[134]
Brazil
[edit]
Compared to 19th-century United States, 20th-century Brazil was characterized by a perceived relative absence of sharply defined racial groups. According to anthropologist Marvin Harris, this pattern reflects a different history and different social relations.
Race in Brazil was "biologized", but in a way that recognized the difference between ancestry (which determines genotype) and phenotypic differences. There, racial identity was not governed by rigid descent rule, such as the one-drop rule, as it was in the United States. A Brazilian child was never automatically identified with the racial type of one or both parents, nor were there only a very limited number of categories to choose from,[135] to the extent that full siblings can pertain to different racial groups.[136]
| Self-reported ancestry of people from Rio de Janeiro, by race or skin color (2000 survey)[137] | |||
|---|---|---|---|
| Ancestry | brancos | pardos | negros |
| European only | 48% | 6% | – |
| African only | – | 12% | 25% |
| Amerindian only | – | 2% | – |
| African and European | 23% | 34% | 31% |
| Amerindian and European | 14% | 6% | – |
| African and Amerindian | – | 4% | 9% |
| African, Amerindian and European | 15% | 36% | 35% |
| Total | 100% | 100% | 100% |
| Any African | 38% | 86% | 100% |
Over a dozen racial categories would be recognized in conformity with all the possible combinations of hair color, hair texture, eye color, and skin color. These types grade into each other like the colors of the spectrum, and not one category stands significantly isolated from the rest. That is, race referred preferentially to appearance, not heredity, and appearance is a poor indication of ancestry, because only a few genes are responsible for someone's skin color and traits: a person who is considered white may have more African ancestry than a person who is considered black, and the reverse can be also true about European ancestry.[138] The complexity of racial classifications in Brazil reflects the extent of genetic mixing in Brazilian society, a society that remains highly, but not strictly, stratified along color lines. These socioeconomic factors are also significant to the limits of racial lines, because a minority of pardos, or brown people, are likely to start declaring themselves white or black if socially upward,[139] and being seen as relatively "whiter" as their perceived social status increases (much as in other regions of Latin America).[140]
Fluidity of racial categories aside, the "biologification" of race in Brazil referred above would match contemporary concepts of race in the United States quite closely, though, if Brazilians are supposed to choose their race as one among, Asian and Indigenous apart, three IBGE's census categories. While assimilated Amerindians and people with very high quantities of Amerindian ancestry are usually grouped as caboclos, a subgroup of pardos which roughly translates as both mestizo and hillbilly, for those of lower quantity of Amerindian descent a higher European genetic contribution is expected to be grouped as a pardo. In several genetic tests, people with less than 60–65% of European descent and 5–10% of Amerindian descent usually cluster with Afro-Brazilians (as reported by the individuals), or 6.9% of the population, and those with about 45% or more of Subsaharan contribution most times do so (in average, Afro-Brazilian DNA was reported to be about 50% Subsaharan African, 37% European and 13% Amerindian).[141][142][143][144]
| Ethnic groups in Brazil (census data)[145] | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Ethnic group | white | black | multiracial | |||||||
| 1872 | 3,787,289 | 1,954,452 | 4,188,737 | |||||||
| 1940 | 26,171,778 | 6,035,869 | 8,744,365 | |||||||
| 1991 | 75,704,927 | 7,335,136 | 62,316,064 | |||||||
| Ethnic groups in Brazil (1872 and 1890)[146] | ||||
|---|---|---|---|---|
| Years | whites | multiracial | blacks | Indians |
| 1872 | 38.1% | 38.3% | 19.7% | 3.9% |
| 1890 | 44.0% | 32.4% | 14.6% | 9% |
If a more consistent report with the genetic groups in the gradation of genetic mixing is to be considered (e.g. that would not cluster people with a balanced degree of African and non-African ancestry in the black group instead of the multiracial one, unlike elsewhere in Latin America where people of high quantity of African descent tend to classify themselves as mixed), more people would report themselves as white and pardo in Brazil (47.7% and 42.4% of the population as of 2010, respectively), because by research its population is believed to have between 65 and 80% of autosomal European ancestry, in average (also >35% of European mt-DNA and >95% of European Y-DNA).[141][147][148][149]
From the last decades of the Empire until the 1950s, the proportion of the white population increased significantly while Brazil welcomed 5.5 million immigrants between 1821 and 1932, not much behind its neighbor Argentina with 6.4 million,[150] and it received more European immigrants in its colonial history than the United States. Between 1500 and 1760, 700.000 Europeans settled in Brazil, while 530.000 Europeans settled in the United States for the same given time.[151] Thus, the historical construction of race in Brazilian society dealt primarily with gradations between persons of majority European ancestry and little minority groups with otherwise lower quantity therefrom in recent times.
European Union
[edit]According to the Council of the European Union:
The European Union rejects theories which attempt to determine the existence of separate human races.
— Directive 2000/43/EC[152]
The European Union uses the terms racial origin and ethnic origin synonymously in its documents and according to it "the use of the term 'racial origin' in this directive does not imply an acceptance of such [racial] theories".[152][153][full citation needed] Haney López warns that using "race" as a category within the law tends to legitimize its existence in the popular imagination. In the diverse geographic context of Europe, ethnicity and ethnic origin are arguably more resonant and are less encumbered by the ideological baggage associated with "race". In European context, historical resonance of "race" underscores its problematic nature. In some states, it is strongly associated with laws promulgated by the Nazi and Fascist governments in Europe during the 1930s and 1940s. Indeed, in 1996, the European Parliament adopted a resolution stating that "the term should therefore be avoided in all official texts".[154]
The concept of racial origin relies on the notion that human beings can be separated into biologically distinct "races", an idea generally rejected by the scientific community. Since all human beings belong to the same species, the ECRI (European Commission against Racism and Intolerance) rejects theories based on the existence of different "races". However, in its Recommendation ECRI uses this term in order to ensure that those persons who are generally and erroneously perceived as belonging to "another race" are not excluded from the protection provided for by the legislation. The law claims to reject the existence of "race", yet penalize situations where someone is treated less favourably on this ground.[154]
United States
[edit]The immigrants to the United States came from every region of Europe, Africa, and Asia. They mixed among themselves and with the indigenous inhabitants of the continent. In the United States most people who self-identify as African American have some European ancestors, while many people who identify as European American have some African or Amerindian ancestors.[citation needed]
Since the early history of the United States, Amerindians, African Americans, and European Americans have been classified as belonging to different races. Efforts to track mixing between groups led to a proliferation of categories, such as mulatto and octoroon. The criteria for membership in these races diverged in the late 19th century. During the Reconstruction era, increasing numbers of Americans began to consider anyone with "one drop" of known "Black blood" to be Black, regardless of appearance. By the early 20th century, this notion was made statutory in many states. Amerindians continue to be defined by a certain percentage of "Indian blood" (called blood quantum). To be White one had to have perceived "pure" White ancestry. The one-drop rule or hypodescent rule refers to the convention of defining a person as racially black if he or she has any known African ancestry. This rule meant that those that were mixed race but with some discernible African ancestry were defined as black. The one-drop rule is specific to not only those with African ancestry but to the United States, making it a particularly African-American experience.[155]
The decennial censuses conducted since 1790 in the United States created an incentive to establish racial categories and fit people into these categories.[156]
The term "Hispanic" as an ethnonym emerged in the 20th century with the rise of migration of laborers from the Spanish-speaking countries of Latin America to the United States. Today, the word "Latino" is often used as a synonym for "Hispanic". The definitions of both terms are non-race specific, and include people who consider themselves to be of distinct races (Black, White, Amerindian, Asian, and mixed groups).[157] However, there is a common misconception in the US that Hispanic/Latino is a race[158] or sometimes even that national origins such as Mexican, Cuban, Colombian, Salvadoran, etc. are races. In contrast to "Latino" or "Hispanic", "Anglo" refers to non-Hispanic White Americans or non-Hispanic European Americans, most of whom speak the English language but are not necessarily of English descent.
Views across disciplines over time
[edit]Anthropology
[edit]The concept of race classification in physical anthropology lost credibility around the 1960s and is now considered untenable.[159][160][161] A 2019 statement by the American Association of Physical Anthropologists declares:
Race does not provide an accurate representation of human biological variation. It was never accurate in the past, and it remains inaccurate when referencing contemporary human populations. Humans are not divided biologically into distinct continental types or racial genetic clusters. Instead, the Western concept of race must be understood as a classification system that emerged from, and in support of, European colonialism, oppression, and discrimination.[86]
Wagner et al. (2017) surveyed 3,286 American anthropologists' views on race and genetics, including both cultural and biological anthropologists. They found a consensus among them that biological races do not exist in humans, but that race does exist insofar as the social experiences of members of different races can have significant effects on health.[162]
Wang, Štrkalj et al. (2003) examined the use of race as a biological concept in research papers published in China's only biological anthropology journal, Acta Anthropologica Sinica. The study showed that the race concept was widely used among Chinese anthropologists.[163][164] In a 2007 review paper, Štrkalj suggested that the stark contrast of the racial approach between the United States and China was due to the fact that race is a factor for social cohesion among the ethnically diverse people of China, whereas "race" is a very sensitive issue in America and the racial approach is considered to undermine social cohesion – with the result that in the socio-political context of US academics scientists are encouraged not to use racial categories, whereas in China they are encouraged to use them.[165]
Lieberman et al. in a 2004 study researched the acceptance of race as a concept among anthropologists in the United States, Canada, the Spanish speaking areas, Europe, Russia and China. Rejection of race ranged from high to low, with the highest rejection rate in the United States and Canada, a moderate rejection rate in Europe, and the lowest rejection rate in Russia and China. Methods used in the studies reported included questionnaires and content analysis.[21]
Kaszycka et al. (2009) in 2002–2003 surveyed European anthropologists' opinions toward the biological race concept. Three factors – country of academic education, discipline, and age – were found to be significant in differentiating the replies. Those educated in Western Europe, physical anthropologists, and middle-aged persons rejected race more frequently than those educated in Eastern Europe, people in other branches of science, and those from both younger and older generations. "The survey shows that the views on race are sociopolitically (ideologically) influenced and highly dependent on education."[166]
United States
[edit]Since the second half of the 20th century, physical anthropology in the United States has moved away from a typological understanding of human biological diversity towards a genomic and population-based perspective. Anthropologists have tended to understand race as a social classification of humans based on phenotype and ancestry as well as cultural factors, as the concept is understood in the social sciences.[92][160] Since 1932, an increasing number of college textbooks introducing physical anthropology have rejected race as a valid concept: from 1932 to 1976, only seven out of thirty-two rejected race; from 1975 to 1984, thirteen out of thirty-three rejected race; from 1985 to 1993, thirteen out of nineteen rejected race. According to one academic journal entry, where 78 percent of the articles in the 1931 Journal of Physical Anthropology employed these or nearly synonymous terms reflecting a bio-race paradigm, only 36 percent did so in 1965, and just 28 percent did in 1996.[167]
A 1998 "Statement on 'Race'" composed by a select committee of anthropologists and issued by the executive board of the American Anthropological Association, which they argue "represents generally the contemporary thinking and scholarly positions of a majority of anthropologists", declares:[168]
In the United States both scholars and the general public have been conditioned to viewing human races as natural and separate divisions within the human species based on visible physical differences. With the vast expansion of scientific knowledge in this century, however, it has become clear that human populations are not unambiguous, clearly demarcated, biologically distinct groups. Evidence from the analysis of genetics (e.g., DNA) indicates that most physical variation, about 94%, lies within so-called racial groups. Conventional geographic "racial" groupings differ from one another only in about 6% of their genes. This means that there is greater variation within "racial" groups than between them. In neighboring populations there is much overlapping of genes and their phenotypic (physical) expressions. Throughout history whenever different groups have come into contact, they have interbred. The continued sharing of genetic materials has maintained all of humankind as a single species. ... With the vast expansion of scientific knowledge in this century, ... it has become clear that human populations are not unambiguous, clearly demarcated, biologically distinct groups. ... Given what we know about the capacity of normal humans to achieve and function within any culture, we conclude that present-day inequalities between so-called "racial" groups are not consequences of their biological inheritance but products of historical and contemporary social, economic, educational, and political circumstances.
An earlier survey, conducted in 1985 (Lieberman et al. 1992), asked 1,200 American scientists how many disagree with the following proposition: "There are biological races in the species Homo sapiens." Among anthropologists, the responses were:
Lieberman's study also showed that more women reject the concept of race than men.[170]
The same survey, conducted again in 1999,[171] showed that the number of anthropologists disagreeing with the idea of biological race had risen substantially. The results were as follows:
A line of research conducted by Cartmill (1998), however, seemed to limit the scope of Lieberman's finding that there was "a significant degree of change in the status of the race concept". Goran Štrkalj has argued that this may be because Lieberman and collaborators had looked at all the members of the American Anthropological Association irrespective of their field of research interest, while Cartmill had looked specifically at biological anthropologists interested in human variation.[172]
In 2007, Ann Morning interviewed over 40 American biologists and anthropologists and found significant disagreements over the nature of race, with no one viewpoint holding a majority among either group. Morning also argues that a third position, "antiessentialism", which holds that race is not a useful concept for biologists, should be introduced into this debate in addition to "constructionism" and "essentialism".[173]
According to the 2000 University of Wyoming edition of a popular physical anthropology textbook, forensic anthropologists are overwhelmingly in support of the idea of the basic biological reality of human races.[174] Forensic physical anthropologist and professor George W. Gill has said that the idea that race is only skin deep "is simply not true, as any experienced forensic anthropologist will affirm" and "Many morphological features tend to follow geographic boundaries coinciding often with climatic zones. This is not surprising since the selective forces of climate are probably the primary forces of nature that have shaped human races with regard not only to skin color and hair form but also the underlying bony structures of the nose, cheekbones, etc. (For example, more prominent noses humidify air better.)" While he can see good arguments for both sides, the complete denial of the opposing evidence "seems to stem largely from socio-political motivation and not science at all". He also states that many biological anthropologists see races as real yet "not one introductory textbook of physical anthropology even presents that perspective as a possibility. In a case as flagrant as this, we are not dealing with science but rather with blatant, politically motivated censorship".[174]
In partial response to Gill's statement, Professor of Biological Anthropology C. Loring Brace argues that the reason laymen and biological anthropologists can determine the geographic ancestry of an individual can be explained by the fact that biological characteristics are clinally distributed across the planet, and that does not translate into the concept of race. He states:
Well, you may ask, why can't we call those regional patterns "races"? In fact, we can and do, but it does not make them coherent biological entities. "Races" defined in such a way are products of our perceptions. ... We realize that in the extremes of our transit – Moscow to Nairobi, perhaps – there is a major but gradual change in skin color from what we euphemistically call white to black, and that this is related to the latitudinal difference in the intensity of the ultraviolet component of sunlight. What we do not see, however, is the myriad other traits that are distributed in a fashion quite unrelated to the intensity of ultraviolet radiation. Where skin color is concerned, all the northern populations of the Old World are lighter than the long-term inhabitants near the equator. Although Europeans and Chinese are obviously different, in skin color they are closer to each other than either is to equatorial Africans. But if we test the distribution of the widely known ABO blood-group system, then Europeans and Africans are closer to each other than either is to Chinese.[175]
The concept of "race" is still sometimes used within forensic anthropology (when analyzing skeletal remains), biomedical research, and race-based medicine.[176][177] Brace has criticized forensic anthropologists for this, arguing that they in fact should be talking about regional ancestry. He argues that while forensic anthropologists can determine that a skeletal remain comes from a person with ancestors in a specific region of Africa, categorizing that skeletal as being "black" is a socially constructed category that is only meaningful in the particular social context of the United States, and which is not itself scientifically valid.[178]
Biology, anatomy, and medicine
[edit]In the same 1985 survey (Lieberman et al. 1992), 16% of the surveyed biologists and 36% of the surveyed developmental psychologists disagreed with the proposition: "There are biological races in the species Homo sapiens."
The authors of the study also examined 77 college textbooks in biology and 69 in physical anthropology published between 1932 and 1989. Physical anthropology texts argued that biological races exist until the 1970s, when they began to argue that races do not exist. In contrast, biology textbooks did not undergo such a reversal but many instead dropped their discussion of race altogether. The authors attributed this to biologists trying to avoid discussing the political implications of racial classifications, and to the ongoing discussions in biology about the validity of the idea of "subspecies". The authors concluded, "The concept of race, masking the overwhelming genetic similarity of all peoples and the mosaic patterns of variation that do not correspond to racial divisions, is not only socially dysfunctional but is biologically indefensible as well (pp. 5 18–5 19)."(Lieberman et al. 1992, pp. 316–17)
A 1994 examination of 32 English sport/exercise science textbooks found that 7 (21.9%) claimed that there are biophysical differences due to race that might explain differences in sports performance, 24 (75%) did not mention nor refute the concept, and 1 (3.1%) expressed caution with the idea.[179]
In February 2001, the editors of Archives of Pediatrics and Adolescent Medicine asked "authors to not use race and ethnicity when there is no biological, scientific, or sociological reason for doing so".[180] The editors also stated that "analysis by race and ethnicity has become an analytical knee-jerk reflex".[181] Nature Genetics now ask authors to "explain why they make use of particular ethnic groups or populations, and how classification was achieved".[182]
Morning (2008) looked at high school biology textbooks during the 1952–2002 period and initially found a similar pattern with only 35% directly discussing race in the 1983–92 period from initially 92% doing so. However, this has increased somewhat after this to 43%. More indirect and brief discussions of race in the context of medical disorders have increased from none to 93% of textbooks. In general, the material on race has moved from surface traits to genetics and evolutionary history. The study argues that the textbooks' fundamental message about the existence of races has changed little.[183]
Surveying views on race in the scientific community in 2008, Morning concluded that biologists had failed to come to a clear consensus, and they often split along cultural and demographic lines. She notes: "At best, one can conclude that biologists and anthropologists now appear equally divided in their beliefs about the nature of race."[173]
Gissis (2008) examined several important American and British journals in genetics, epidemiology and medicine for their content during the 1946–2003 period. He wrote that "Based upon my findings I argue that the category of race only seemingly disappeared from scientific discourse after World War II and has had a fluctuating yet continuous use during the time span from 1946 to 2003, and has even become more pronounced from the early 1970s on".[184]
33 health services researchers from differing geographic regions were interviewed in a 2008 study. The researchers recognized the problems with racial and ethnic variables but the majority still believed these variables were necessary and useful.[185]
A 2010 examination of 18 widely used English anatomy textbooks found that they all represented human biological variation in superficial and outdated ways, many of them making use of the race concept in ways that were current in 1950s anthropology. The authors recommended that anatomical education should describe human anatomical variation in more detail and rely on newer research that demonstrates the inadequacies of simple racial typologies.[186]
A 2021 study that examined over 11,000 papers from 1949 to 2018 in the American Journal of Human Genetics, found that "race" was used in only 5% of papers published in the last decade, down from 22% in the first. Together with an increase in use of the terms "ethnicity", "ancestry", and location-based terms, it suggests that human geneticists have mostly abandoned the term "race".[187]
The National Academies of Sciences, Engineering, and Medicine (NASEM), supported by the US the National Institutes of Health, formally declared that "researchers should not use race as a proxy for describing human genetic variation".[188] The report of its Committee on the Use of Race, Ethnicity, and Ancestry as Population Descriptors in Genomics Research titled Using Population Descriptors in Genetics and Genomics Research was released on 14 March 2023.[189][27] The report stated: "In humans, race is a socially constructed designation, a misleading and harmful surrogate for population genetic differences, and has a long history of being incorrectly identified as the major genetic reason for phenotypic differences between groups."[3] The committee co-chair Charmaine D. Royal and Robert O. Keohane of Duke University agreed in the meeting: "Classifying people by race is a practice entangled with and rooted in racism."[188]
Sociology
[edit]Lester Frank Ward (1841–1913), considered to be one of the founders of American sociology, rejected notions that there were fundamental differences that distinguished one race from another, although he acknowledged that social conditions differed dramatically by race.[190] At the turn of the 20th century, sociologists viewed the concept of race in ways that were shaped by the scientific racism of the 19th and early 20th centuries.[191] Many sociologists focused on African Americans, called Negroes at that time, and claimed that they were inferior to whites. White sociologist Charlotte Perkins Gilman (1860–1935), for example, used biological arguments to claim the inferiority of African Americans.[191] American sociologist Charles H. Cooley (1864–1929) theorized that differences among races were "natural", and that biological differences result in differences in intellectual abilities.[192][190] Edward Alsworth Ross (1866–1951), also an important figure in the founding of American sociology, and a eugenicist, believed that whites were the superior race, and that there were essential differences in "temperament" among races.[190] In 1910, the Journal published an article by Ulysses G. Weatherly (1865–1940) that called for white supremacy and segregation of the races to protect racial purity.[190]
W. E. B. Du Bois (1868–1963), one of the first African-American sociologists, was the first sociologist to use sociological concepts and empirical research methods to analyze race as a social construct instead of a biological reality.[191] Beginning in 1899 with his book The Philadelphia Negro, Du Bois studied and wrote about race and racism throughout his career. In his work, he contended that social class, colonialism, and capitalism shaped ideas about race and racial categories. Social scientists largely abandoned scientific racism and biological reasons for racial categorization schemes by the 1930s.[193] Other early sociologists, especially those associated with the Chicago School, joined Du Bois in theorizing race as a socially constructed fact.[193] By 1978, William Julius Wilson argued that race and racial classification systems were declining in significance, and that instead, social class more accurately described what sociologists had earlier understood as race.[194] By 1986, sociologists Michael Omi and Howard Winant successfully introduced the concept of racial formation to describe the process by which racial categories are created.[195] Omi and Winant assert that "there is no biological basis for distinguishing among human groups along the lines of race".[195]
Eduardo Bonilla-Silva, Sociology professor at Duke University, remarks:[196] "I contend that racism is, more than anything else, a matter of group power; it is about a dominant racial group (whites) striving to maintain its systemic advantages and minorities fighting to subvert the racial status quo."[197] The types of practices that take place under this new color-blind racism is subtle, institutionalized, and supposedly not racial. Color-blind racism thrives on the idea that race is no longer an issue in the United States.[197] There are contradictions between the alleged color-blindness of most whites and the persistence of a color-coded system of inequality.[citation needed]
Today, sociologists generally understand race and racial categories as socially constructed, and reject racial categorization schemes that depend on biological differences.[193]
Political and practical uses
[edit]Biomedicine
[edit]In the United States, federal government policy promotes the use of racially categorized data to identify and address health disparities between racial or ethnic groups.[198] In clinical settings, race has sometimes been considered in the diagnosis and treatment of medical conditions. Doctors have noted that some medical conditions are more prevalent in certain racial or ethnic groups than in others, without being sure of the cause of those differences. Recent interest in race-based medicine, or race-targeted pharmacogenomics, has been fueled by the proliferation of human genetic data which followed the decoding of the human genome in the first decade of the twenty-first century. There is an active debate among biomedical researchers about the meaning and importance of race in their research. Proponents of the use of racial categories in biomedicine argue that continued use of racial categorizations in biomedical research and clinical practice makes possible the application of new genetic findings, and provides a clue to diagnosis.[199][200] Biomedical researchers' positions on race fall into two main camps: those who consider the concept of race to have no biological basis and those who consider it to have the potential to be biologically meaningful. Members of the latter camp often base their arguments around the potential to create genome-based personalized medicine.[201]
Other researchers point out that finding a difference in disease prevalence between two socially defined groups does not necessarily imply genetic causation of the difference.[202][203] They suggest that medical practices should maintain their focus on the individual rather than an individual's membership to any group.[204] They argue that overemphasizing genetic contributions to health disparities carries various risks such as reinforcing stereotypes, promoting racism or ignoring the contribution of non-genetic factors to health disparities.[205] International epidemiological data show that living conditions rather than race make the biggest difference in health outcomes even for diseases that have "race-specific" treatments.[206] Some studies have found that patients are reluctant to accept racial categorization in medical practice.[200]
Law enforcement
[edit]In an attempt to provide general descriptions that may facilitate the job of law enforcement officers seeking to apprehend suspects, the United States FBI employs the term "race" to summarize the general appearance (skin color, hair texture, eye shape, and other such easily noticed characteristics) of individuals whom they are attempting to apprehend. From the perspective of law enforcement officers, it is generally more important to arrive at a description that will readily suggest the general appearance of an individual than to make a scientifically valid categorization by DNA or other such means. Thus, in addition to assigning a wanted individual to a racial category, such a description will include: height, weight, eye color, scars and other distinguishing characteristics.
Criminal justice agencies in England and Wales use at least two separate racial/ethnic classification systems when reporting crime, as of 2010. One is the system used in the 2001 Census when individuals identify themselves as belonging to a particular ethnic group: W1 (White-British), W2 (White-Irish), W9 (Any other white background); M1 (White and black Caribbean), M2 (White and black African), M3 (White and Asian), M9 (Any other mixed background); A1 (Asian-Indian), A2 (Asian-Pakistani), A3 (Asian-Bangladeshi), A9 (Any other Asian background); B1 (Black Caribbean), B2 (Black African), B3 (Any other black background); O1 (Chinese), O9 (Any other). The other is categories used by the police when they visually identify someone as belonging to an ethnic group, e.g. at the time of a stop and search or an arrest: White – North European (IC1), White – South European (IC2), Black (IC3), Asian (IC4), Chinese, Japanese, or South East Asian (IC5), Middle Eastern (IC6), and Unknown (IC0). "IC" stands for "Identification Code;" these items are also referred to as Phoenix classifications.[207] Officers are instructed to "record the response that has been given" even if the person gives an answer which may be incorrect; their own perception of the person's ethnic background is recorded separately.[208] Comparability of the information being recorded by officers was brought into question by the Office for National Statistics (ONS) in September 2007, as part of its Equality Data Review; one problem cited was the number of reports that contained an ethnicity of "Not Stated".[209]
In many countries, such as France, the state is legally banned from maintaining data based on race.[210]
In the United States, the practice of racial profiling has been ruled to be both unconstitutional and a violation of civil rights. There is active debate regarding the cause of a marked correlation between the recorded crimes, punishments meted out, and the country's populations. Many consider de facto racial profiling an example of institutional racism in law enforcement.[211]
Mass incarceration in the United States disproportionately impacts African American and Latino communities. Michelle Alexander, author of The New Jim Crow: Mass Incarceration in the Age of Colorblindness (2010), argues that mass incarceration is best understood as not only a system of overcrowded prisons. Mass incarceration is also, "the larger web of laws, rules, policies, and customs that control those labeled criminals both in and out of prison".[212] She defines it further as "a system that locks people not only behind actual bars in actual prisons, but also behind virtual bars and virtual walls", illustrating the second-class citizenship that is imposed on a disproportionate number of people of color, specifically African-Americans. She compares mass incarceration to Jim Crow laws, stating that both work as racial caste systems.[213]
Many research findings appear to agree that the impact of victim race in the interpersonal violence (IPV) arrest decision might include a racial bias in favor of white victims. A 2011 study in a national sample of IPV arrests found that female arrest was more likely if the male victim was white and the female offender was black, while male arrest was more likely if the female victim was white. For both female and male arrest in IPV cases, situations involving married couples were more likely to lead to arrest compared to dating or divorced couples. More research is needed to understand agency and community factors that influence police behavior and how discrepancies in IPV interventions/ tools of justice can be addressed.[214]
Recent work using DNA cluster analysis to determine race background has been used by some criminal investigators to narrow their search for the identity of both suspects and victims.[215] Proponents of DNA profiling in criminal investigations cite cases where leads based on DNA analysis proved useful, but the practice remains controversial among medical ethicists, defense lawyers and some in law enforcement.[216]
The Constitution of Australia contains a line about 'people of any race for whom it is deemed necessary to make special laws', despite there being no agreed definition of race described in the document.
Forensic anthropology
[edit]Similarly, forensic anthropologists draw on highly heritable morphological features of human remains (e.g. cranial measurements) to aid in the identification of the body, including in terms of race. In a 1992 article, anthropologist Norman Sauer noted that anthropologists had generally abandoned the concept of race as a valid representation of human biological diversity, except for forensic anthropologists. He asked, "If races don't exist, why are forensic anthropologists so good at identifying them?"[161] He concluded:
[T]he successful assignment of race to a skeletal specimen is not a vindication of the race concept, but rather a prediction that an individual, while alive was assigned to a particular socially constructed "racial" category. A specimen may display features that point to African ancestry. In this country that person is likely to have been labeled Black regardless of whether or not such a race actually exists in nature.[161]
Identification of the ancestry of an individual is dependent upon knowledge of the frequency and distribution of phenotypic traits in a population. This does not necessitate the use of a racial classification scheme based on unrelated traits, although the race concept is widely used in medical and legal contexts in the United States.[217] Some studies have reported that races can be identified with a high degree of accuracy using certain methods, such as that developed by Giles and Elliot. However, this method sometimes fails to be replicated in other times and places; for instance, when the method was re-tested to identify Native Americans, the average rate of accuracy dropped from 85% to 33%.[78] Prior information about the individual (e.g. Census data) is also important in allowing the accurate identification of the individual's "race".[218]
In a different approach, anthropologist C. Loring Brace said:
The simple answer is that, as members of the society that poses the question, they are inculcated into the social conventions that determine the expected answer. They should also be aware of the biological inaccuracies contained in that "politically correct" answer. Skeletal analysis provides no direct assessment of skin color, but it does allow an accurate estimate of original geographical origins. African, eastern Asian, and European ancestry can be specified with a high degree of accuracy. Africa of course entails "black", but "black" does not entail African.[178]
In association with a NOVA program in 2000 about race, he wrote an essay opposing use of the term.[219]
A 2002 study found that about 13% of human craniometric variation existed between regions, while 6% existed between local populations within regions and 81% within local populations. In contrast, the opposite pattern of genetic variation was observed for skin color (which is often used to define race), with 88% of variation between regions. The study concluded: "The apportionment of genetic diversity in skin color is atypical, and cannot be used for purposes of classification."[220] Similarly, a 2009 study found that craniometrics could be used accurately to determine what part of the world someone was from based on their cranium; however, this study also found that there were no abrupt boundaries that separated craniometric variation into distinct racial groups.[221] Another 2009 study showed that American blacks and whites had different skeletal morphologies, and that significant patterning in variation in these traits exists within continents. This suggests that classifying humans into races based on skeletal characteristics would necessitate many different "races" being defined.[222]
In 2010, philosopher Neven Sesardić argued that when several traits are analyzed at the same time, forensic anthropologists can classify a person's race with an accuracy of close to 100% based on only skeletal remains.[223] Sesardić's claim has been disputed by philosopher Massimo Pigliucci, who accused Sesardić of "cherry pick[ing] the scientific evidence and reach[ing] conclusions that are contradicted by it". Specifically, Pigliucci argued that Sesardić misrepresented a paper by Ousley et al. (2009), and neglected to mention that they identified differentiation not just between individuals from different races, but also between individuals from different tribes, local environments, and time periods.[224]
See also
[edit]- Casta
- Clan
- Cultural identity
- Ethnic nationalism
- Ethnic stereotype
- Genetic distance
- History of anthropometry § Race, identity and cranio-facial description
- Human skin color
- Interracial marriage
- List of contemporary ethnic groups
- Melanism
- Minzu (anthropology)
- Multiracial
- Race and ethnicity in censuses (US)
- Race and ethnicity in Latin America
- Racialization
- Raciolinguistics
- UNESCO statements on race
- All pages with titles beginning with Racial
- Race (French Constitution)
References
[edit]- ^ a b c d e Barnshaw, John (2008). "Race". In Schaefer, Richard T. (ed.). Encyclopedia of Race, Ethnicity, and Society. Vol. 1. Sage Publications. pp. 1091–1093. ISBN 978-1-45-226586-5.
- ^ Roediger, David R. "Historical Foundations of Race". National Museum of African American History and Culture.
- ^ a b Using Population Descriptors in Genetics and Genomics Research: A New Framework for an Evolving Field (Consensus Study Report). National Academies of Sciences, Engineering, and Medicine. 2023. doi:10.17226/26902. ISBN 978-0-309-70065-8. PMID 36989389.
In humans, race is a socially constructed designation, a misleading and harmful surrogate for population genetic differences, and has a long history of being incorrectly identified as the major genetic reason for phenotypic differences between groups.
- ^ Amutah, C.; Greenidge, K.; Mante, A.; Munyikwa, M.; Surya, S. L.; Higginbotham, E.; Jones, D. S.; Lavizzo-Mourey, R.; Roberts, D.; Tsai, J.; Aysola, J. (March 2021). Malina, D. (ed.). "Misrepresenting Race — The Role of Medical Schools in Propagating Physician Bias". The New England Journal of Medicine. 384 (9). Massachusetts Medical Society: 872–878. doi:10.1056/NEJMms2025768. ISSN 1533-4406. PMID 33406326. S2CID 230820421.
- ^ Gannon, Megan (5 February 2016). "Race Is a Social Construct, Scientists Argue". Scientific American. ISSN 0036-8733. Archived from the original on 14 February 2023. Retrieved 1 March 2023.
- ^ a b Smedley, Audrey; Takezawa, Yasuko I.; Wade, Peter. "Race: Human". Encyclopædia Britannica. Encyclopædia Britannica Inc. Retrieved 22 August 2017.
- ^ Yudell, M.; Roberts, D.; DeSalle, R.; Tishkoff, S. (5 February 2016). "Taking race out of human genetics". Science. 351 (6273). American Association for the Advancement of Science: 564–565. Bibcode:2016Sci...351..564Y. doi:10.1126/science.aac4951. ISSN 0036-8075. PMID 26912690. S2CID 206639306.
- ^ See:
- ^ Sober (2000), pp. 148–151.
- ^ a b Lee et al. 2008: "We caution against making the naive leap to a genetic explanation for group differences in complex traits, especially for human behavioral traits such as IQ scores"
- ^ AAA 1998: "For example, 'Evidence from the analysis of genetics (e.g., DNA) indicates that most physical variation, about 94%, lies within so-called racial groups. Conventional geographic "racial" groupings differ from one another only in about 6% of their genes. This means that there is greater variation within 'racial' groups than between them.'"
- ^ Keita et al. 2004. "Modern human biological variation is not structured into phylogenetic subspecies ('races'), nor are the taxa of the standard anthropological 'racial' classifications breeding populations. The 'racial taxa' do not meet the phylogenetic criteria. 'Race' denotes socially constructed units as a function of the incorrect usage of the term."
- ^ Harrison, Guy (2010). Race and Reality. Amherst, New York: Prometheus Books.
Race is a poor empirical description of the patterns of difference that we encounter within our species. The billions of humans alive today simply do not fit into neat and tidy biological boxes called races. Science has proven this conclusively. The concept of race ... is not scientific and goes against what is known about our ever-changing and complex biological diversity.
- ^ Roberts, Dorothy (2011). Fatal Invention. London / New York: The New Press.
The genetic differences that exist among populations are characterized by gradual changes across geographic regions, not sharp, categorical distinctions. Groups of people across the globe have varying frequencies of polymorphic genes, which are genes with any of several differing nucleotide sequences. There is no such thing as a set of genes that belongs exclusively to one group and not to another. The clinal, gradually changing nature of geographic genetic difference is complicated further by the migration and mixing that human groups have engaged in since prehistory. Human beings do not fit the zoological definition of race. A mountain of evidence assembled by historians, anthropologists, and biologists proves that race is not and cannot be a natural division of human beings.
- ^ Fuentes, Agustín (9 April 2012). "Race Is Real, but not in the way Many People Think". Psychology Today.
- ^ The Royal Institution - panel discussion - What Science Tells us about Race and Racism. 16 March 2016. Archived from the original on 11 December 2021.
- ^ a b Jorde, Lynn B.; Wooding, Stephen P. (2004). "Genetic variation, classification, and 'race'". Nature. 36 (11 Suppl). Nature Research: S28 – S33. doi:10.1038/ng1435. ISSN 1476-4687. PMID 15508000. S2CID 15251775.
Ancestry, then, is a more subtle and complex description of an individual's genetic makeup than is race. This is in part a consequence of the continual mixing and migration of human populations throughout history. Because of this complex and interwoven history, many loci must be examined to derive even an approximate portrayal of individual ancestry.
- ^ White, Michael (30 May 2014). "Why Your Race Isn't Genetic". Pacific Standard. Retrieved 13 December 2014.
[O]ngoing contacts, plus the fact that we were a small, genetically homogeneous species to begin with, has resulted in relatively close genetic relationships, despite our worldwide presence. The DNA differences between humans increase with geographical distance, but boundaries between populations are, as geneticists Kenneth Weiss and Jeffrey Long put it, "multilayered, porous, ephemeral, and difficult to identify". Pure, geographically separated ancestral populations are an abstraction: "There is no reason to think that there ever were isolated, homogeneous parental populations at any time in our human past."
- ^ Bryc, Katarzyna; Durand, Eric Y.; Macpherson, Michael; Reich, David; Mountain, Joanna L. (8 January 2015). "The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States" (PDF). American Journal of Human Genetics. 96 (1). Cell Press on behalf of the American Society of Human Genetics: 37–53. doi:10.1016/j.ajhg.2014.11.010. ISSN 0002-9297. PMC 4289685. PMID 25529636. S2CID 3889161. Archived (PDF) from the original on 10 May 2022. Retrieved 1 June 2022.
The relationship between self-reported identity and genetic African ancestry, as well as the low numbers of self-reported African Americans with minor levels of African ancestry, provide insight into the complexity of genetic and social consequences of racial categorization, assortative mating, and the impact of notions of "race" on patterns of mating and self-identity in the US. Our results provide empirical support that, over recent centuries, many individuals with partial African and Native American ancestry have "passed" into the white community, with multiple lines of evidence establishing African and Native American ancestry in self-reported European Americans.
- ^ Zimmer, Carl (24 December 2014). "White? Black? A Murky Distinction Grows Still Murkier". The New York Times. Retrieved 24 December 2014.
On average, the scientists found, people who identified as African-American had genes that were only 73.2 percent African. European genes accounted for 24 percent of their DNA, while 0.8 percent came from Native Americans. Latinos, on the other hand, had genes that were on average 65.1 percent European, 18 percent Native American, and 6.2 percent African. The researchers found that European-Americans had genomes that were on average 98.6 percent European, 0.19 percent African, and 0.18 percent Native American. These broad estimates masked wide variation among individuals.
- ^ a b Lieberman, L.; Kaszycka, K. A.; Martinez Fuentes, A. J.; Yablonsky, L.; Kirk, R. C.; Strkalj, G.; Wang, Q.; Sun, L. (December 2004). "The race concept in six regions: variation without consensus". Collegium Antropologicum. 28 (2): 907–921. PMID 15666627.
- ^ Graves 2001, p. [page needed]
- ^ Keita et al. 2004
- ^ AAPA 1996, p. 714 "Pure races, in the sense of genetically homogeneous populations, do not exist in the human species today, nor is there any evidence that they have ever existed in the past."
- ^ a b "Race2". Oxford Dictionaries. Oxford University Press. Archived from the original on 6 September 2015. Retrieved 5 October 2012.
1. Each of the major division of humankind, having distinct physical characteristics [example elided]. 1.1. mass noun The fact or condition of belonging to a racial division or group; the qualities or characteristics associated with this. 1.2. A group of people sharing the same culture, history, language, etc.; an ethnic group [example elided].
Provides 8 definitions, from biological to literary; only the most pertinent have been quoted. - ^ Keita et al. 2004. "Many terms requiring definition for use describe demographic population groups better than the term 'race' because they invite examination of the criteria for classification."
- ^ a b Zimmer, Carl (14 March 2023). "Guidelines Warn Against Racial Categories in Genetic Research". The New York Times. ISSN 0362-4331. Retrieved 17 April 2023.
- ^ Pillay, Kathryn (2019). "Indian Identity in South Africa". The Palgrave Handbook of Ethnicity. Palgrave Macmillan. pp. 77–92. doi:10.1007/978-981-13-2898-5_9. ISBN 978-981-13-2897-8.
- ^ Wang, Hansi Lo (29 January 2018). "No Middle Eastern Or North African Category On 2020 Census, Bureau Says". NPR. Retrieved 16 August 2019.
- ^ Williams, S. M.; Templeton, A. R. (2003). "Race and Genomics". New England Journal of Medicine. 348 (25): 2581–2582. doi:10.1056/nejm200306193482521. PMID 12815151.
- ^ Templeton 2002, pp. 31–56.
- ^ Olson, Steve (2002). Mapping Human History: Discovering the Past Through Our Genes. Boston: Houghton Mifflin Harcourt.
- ^ a b c Templeton 2013.
- ^ Reich, David (23 March 2018). "How Genetics Is Changing Our Understanding of 'Race'". The New York Times. Archived from the original on 8 September 2019. Retrieved 8 October 2019.
Groundbreaking advances in DNA sequencing technology have been made over the last two decades. These advances enable us to measure with exquisite accuracy what fraction of an individual's genetic ancestry traces back to, say, West Africa 500 years ago – before the mixing in the Americas of the West African and European gene pools that were almost completely isolated for the last 70,000 years. With the help of these tools, we are learning that while race may be a social construct, differences in genetic ancestry that happen to correlate to many of today's racial constructs are real. Recent genetic studies have demonstrated differences across populations not just in the genetic determinants of simple traits such as skin color, but also in more complex traits like bodily dimensions and susceptibility to diseases.
- ^ "How Not To Talk About Race And Genetics". Buzzfeed News. 30 March 2018. Archived from the original on 30 August 2019. Retrieved 8 October 2019.
[The] robust body of scholarship recognizes the existence of geographically based genetic variation in our species, but shows that such variation is not consistent with biological definitions of race. Nor does that variation map precisely onto ever changing socially defined racial groups.
- ^ Lee 1997.
- ^ See:
- ^ See:
- Lee 1997
- Nobles 2000
- Morgan 1975 as cited in Lee 1997, p. 407
- ^ "AABA Statement on Race & Racism". American Association of Biological Anthropologists. 2019.
- ^ See:
- Morgan 1975 as cited in Lee 1997, p. 407
- Smedley 2007
- Sivanandan 1982
- Crenshaw 1988
- Conley 2007
- Winfield 2007: "It was Aristotle who first arranged all animals into a single, graded scale that placed humans at the top as the most perfect iteration. By the late 19th century, the idea that inequality was the basis of natural order, known as the great chain of being, was part of the common lexicon."
- ^ Lee 1997 citing Morgan 1975 and Appiah 1992
- ^ See:
- Sivanandan 1982
- Muffoletto 2003
- McNeilly et al. 1996: Psychiatric instrument called the "Perceived Racism Scale" "provides a measure of the frequency of exposure to many manifestations of racism ... including individual and institutional"; also assesses motional and behavioral coping responses to racism.
- Miles 2000
- ^ Owens & King 1999
- ^ King 2007: For example, "the association of blacks with poverty and welfare ... is due, not to race per se, but to the link that race has with poverty and its associated disadvantages". p. 75.
- ^ Schaefer 2008: "In many parts of Latin America, racial groupings are based less on the biological physical features and more on an intersection between physical features and social features such as economic class, dress, education, and context. Thus, a more fluid treatment allows for the construction of race as an achieved status rather than an ascribed status as is the case in the United States."
- ^ See:
- Brace 2000a
- Gill 2000a
- Lee 1997: "The very naturalness of 'reality' is itself the effect of a particular set of discursive constructions. In this way, discourse does not simply reflect reality, but actually participates in its construction"
- ^ Hartigan, John (June 2008). "Is Race Still Socially Constructed? The Recent Controversy over Race and Medical Genetics". Science as Culture. 17 (2): 163–193. doi:10.1080/09505430802062943. S2CID 18451795.
- ^ a b c Marks 2008, p. 28
- ^ See:
- ^ Keita et al. 2004. "Religious, cultural, social, national, ethnic, linguistic, genetic, geographical and anatomical groups have been and sometimes still are called 'races'"
- ^ Kennedy, Rebecca F. (2013). "Introduction". Race and Ethnicity in the Classical world: An Anthology of Primary Sources in Translation. Hackett Publishing Company. p. xiii. ISBN 978-1-60384-994-4.
The ancients would not understand the social construct we call 'race' any more than they would understand the distinction modem scholars and social scientists generally draw between race and 'ethnicity.' The modern concept of race is a product of the colonial enterprises of European powers from the 16th to 18th centuries that identified race in terms of skin color and physical difference. In the post-Enlightenment world, a 'scientific,' biological idea of race suggested that human difference could be explained by biologically distinct groups of humans, evolved from separate origins, who could be distinguished by physical differences, predominantly skin color .... Such categorizations would have confused the ancient Greeks and Romans.
- ^ Bancel, Nicolas; David, Thomas; Thomas, Dominic, eds. (23 May 2019). "Introduction: The Invention of Race: Scientific and Popular Representations of Race from Linnaeus to the Ethnic Shows". The Invention of Race: Scientific and Popular Representations. Routledge. p. 11. ISBN 978-0-367-20864-6.
'The Invention of Race' has assisted us in the process of locating the 'epistemological moment,' somewhere between 1730 and 1790, when the concept of race was invented and rationalized. A "moment" that was accompanied by a revolution in the way in which the human body was studied and observed in order to formulate scientific conclusions relating to human variability.
- ^ a b Smedley 1999
- ^ Meltzer 1993
- ^ Takaki 1993
- ^ Banton 1977
- ^ For examples see:
- ^ a b Race, Ethnicity, and Genetics Working Group (October 2005). "The Use of Racial, Ethnic, and Ancestral Categories in Human Genetics Research". American Journal of Human Genetics. 77 (4): 519–532. doi:10.1086/491747. PMC 1275602. PMID 16175499.
- ^ Todorov 1993
- ^ Brace 2005, p. 27
- ^ Slotkin 1965, p. 177.
- ^ a b c Graves 2001, p. 39
- ^ Marks 1995
- ^ Graves 2001, pp. 42–43
- ^ Stocking 1968, pp. 38–40
- ^ Hunt, James (24 February 1863). "Introductory address on the study of Anthropology". The Anthropological Review. 1: 3.
... we should always remember, that by whatever means the Negro, for instance, acquired his present physical, mental and moral character, whether he has risen from an ape or descended from a perfect man, we still know that the Races of Europe have now much in their mental and moral nature which the races of Africa have not got.
- ^ Desmond & Moore 2009, pp. 332–341
- ^ Cela-Conde, Camilo J.; Ayala, Francisco J. (2007). Human Evolution Trails from the Past. Oxford University Press. p. 195.
- ^ Lewin, Roger (2005). Human Evolution an illustrated introduction (Fifth ed.). Blackwell Publishing. p. 159.
- ^ Stringer, Chris (2012). Lone Survivors: How We Came to Be the Only Humans on Earth. London: Times Books. ISBN 978-0-8050-8891-5.
- ^ a b Cravens 2010
- ^ Currell & Cogdell 2006
- ^ Hirschman, Charles (2004). "The Origins and Demise of the Concept of Race". Population and Development Review. 30 (3): 385–415. doi:10.1111/j.1728-4457.2004.00021.x. ISSN 1728-4457. S2CID 145485765.
- ^ See:
- ^ See:
- ^ See:
- ^ Wilson & Brown 1953
- ^ a b Goodman, A. H. (November 2000). "Why genes don't count (for racial differences in health)". American Journal of Public Health. 90 (11): 1699–1702. doi:10.2105/ajph.90.11.1699. ISSN 0090-0036. PMC 1446406. PMID 11076233.
- ^ See:
- ^ Haig et al. 2006
- ^ a b Templeton 1998
- ^ Templeton 1998 "Genetic surveys and the analyses of DNA haplotype trees show that human 'races' are not distinct lineages, and that this is not due to recent admixture; human 'races' are not and never were 'pure'."
- ^ Relethford, John H. (23 February 2017). "Biological Anthropology, Population Genetics, and Race". In Zack, Naomi (ed.). The Oxford Handbook of Philosophy and Race. doi:10.1093/oxfordhb/9780190236953.013.20. ISBN 978-0-19-023695-3.
Human populations do not exhibit the levels of geographic isolation or genetic divergence to fit the subspecies model of race.
- ^ Wright 1978
- ^ See:
- ^ a b "AABA Statement on Race & Racism". physanth.org.
- ^ Andreasen 2000
- ^ Marks 2008, p. 28–29.
- ^ Marks 2008.
- ^ a b Lieberman & Jackson 1995
- ^ a b c Hunley, Keith L.; Cabana, Graciela S.; Long, Jeffrey C. (1 December 2015). "The apportionment of human diversity revisited". American Journal of Physical Anthropology. 160 (4): 561–569. doi:10.1002/ajpa.22899. ISSN 1096-8644. PMID 26619959.
- ^ a b Caspari 2003.
- ^ Brace & Montagu 1965, p. [page needed].
- ^ Brace 2000, p. 301.
- ^ a b Livingstone & Dobzhansky 1962
- ^ Ehrlich & Holm 1964
- ^ Weiss 2005
- ^ Marks 2002
- ^ Boyd 1950
- ^ Lieberman & Kirk 1997, p. 195
- ^ Molnar 1992
- ^ Human Genome Project 2003
- ^ Pigliucci, Massimo; Kaplan, Jonathan (December 2003). "On the Concept of Biological Race and Its Applicability to Humans". Philosophy of Science. 70 (5): 1161–1172. doi:10.1086/377397. S2CID 44750046.
- ^ Walsh, Anthony; Yun, Ilhong (October 2011). "Race and Criminology in the Age of Genomic Science". Social Science Quarterly. 92 (5): 1279–1296. doi:10.1111/j.1540-6237.2011.00818.x.
- ^ Bamshad et al. 2004.
- ^ Lewontin 1972.
- ^ Jorde, Lynn B.; Carey, John C.; Bamshad, Michael J.; White, Raymond L. (2000). Medical Genetics (2nd ed.). Mosby. ISBN 978-0-8151-4608-7.[page needed]
- ^ Long 2009, p. 802.
- ^ Romualdi, Chiara; Balding, David; Nasidze, Ivane S.; Risch, Gregory; Robichaux, Myles; Sherry, Stephen T.; Stoneking, Mark; Batzer, Mark A.; Barbujani, Guido (April 2002). "Patterns of human diversity, within and among continents, inferred from biallelic DNA polymorphisms". Genome Research. 12 (4): 602–612. doi:10.1101/gr.214902. ISSN 1088-9051. PMC 187513. PMID 11932244.
- ^ Edwards 2003
- ^ Dawkins, Richard; Wong, Yan (2005). The Ancestor's Tale: A Pilgrimage to the Dawn of Evolution. Houghton Mifflin Harcourt. pp. 406–407. ISBN 978-0-61-861916-0.
(Summarizing Edwards' thesis): We can all happily agree that human racial classification is of no social value and is positively destructive of social and human relations. That is one reason why I object to ticking boxes on forms and why I object to positive discrimination in job selection. But that doesn't mean that race is of 'virtually no genetic or taxonomic significance.' This is Edwards's point, and he reasons as follows. However small the racial partition of total variation may be, if such racial characteristics as there are highly correlated with other racial characteristics, they are by definition informative, and therefore of taxonomic significance.
- ^ See:
- Cavalli-Sforza, Menozzi & Piazza 1994
- Bamshad et al. 2004, p. 599
- Tang et al. 2005
- Rosenberg et al. 2005: "If enough markers are used ... individuals can be partitioned into genetic clusters that match major geographic subdivisions of the globe."
- ^ a b Tang et al. 2005.
- ^ Mountain & Risch 2004
- ^ Gitschier 2005
- ^ a b Witherspoon et al. 2007
- ^ Brace 2005, p. 326
- ^ Kaplan, Jonathan Michael (January 2011) "'Race': What Biology Can Tell Us about a Social Construct". In: Encyclopedia of Life Sciences (ELS). John Wiley & Sons, Ltd: Chichester
- ^ Kaplan, Jonathan Michael; Winther, Rasmus Grønfeldt (2014). "Realism, Antirealism, and Conventionalism About Race". Philosophy of Science. 81 (5): 1039–1052. doi:10.1086/678314. S2CID 55148854.
- ^ a b Winther, Rasmus Grønfeldt (2015). "The Genetic Reification of 'Race'?: A Story of Two Mathematical Methods" (PDF). Critical Philosophy of Race. 2 (2): 204–223.
- ^ Kaplan & Winther (2013).
- ^ Graves, Joseph (7 June 2006). "What We Know and What We Don't Know: Human Genetic Variation and the Social Construction of Race". Race and Genomics. Archived from the original on 3 June 2019. Retrieved 12 September 2007.
- ^ Weiss, K. M.; Fullerton, S. M. (2005). "Racing around, getting nowhere". Evolutionary Anthropology. 14 (5): 165–169. doi:10.1002/evan.20079. S2CID 84927946.
- ^ Mills, Charles W. (1988). "But What Are You Really? The Metaphysics of Race". Blackness visible: essays on philosophy and race. Ithaca, New York: Cornell University Press. pp. 41–66.
- ^ Gannett, Lisa (September 2014). "Biogeographical ancestry and race". Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences. 47: 173–184. doi:10.1016/j.shpsc.2014.05.017. PMID 24989973.
- ^ Barbujani 2005.
- ^ Hunley, Keith L.; Healy, Meghan E.; Long, Jeffrey C. (18 February 2009). "The global pattern of gene identity variation reveals a history of long-range migrations, bottlenecks, and local mate exchange: Implications for biological race" (PDF). American Journal of Physical Anthropology. 139 (1): 35–46. Bibcode:2009AJPA..139...35H. doi:10.1002/ajpa.20932. hdl:2027.42/62159. PMID 19226641.
- ^ Gordon 1964, p. [page needed]
- ^ "New Ideas, New Fuels: Craig Venter at the Oxonian". FORA.tv. 3 November 2008. Archived from the original on 22 January 2009. Retrieved 18 April 2009.
- ^ Palmié 2007.
- ^ Mevorach 2007.
- ^ Perry, Imani (2011). More Beautiful and More Terrible: The Embrace and Transcendence of Racial Inequality in the United States. New York: New York University Press. p. 23.
- ^ Perry, Imani (2011). More Beautiful and More Terrible: The Embrace and Transcendence of Racial Inequality in the United States. New York: New York University Press. p. 24.
- ^ Ford, Richard T. (2005). Racial Culture: A Critique. Princeton University Press. pp. 117–118, 125–128. ISBN 0-691-11960-0.
- ^ Harris 1980
- ^ Parra, F. C.; Amado, R. C.; Lambertucci, J. R.; Rocha, J.; Antunes, C. M.; Pena, S. D. (January 2003). "Color and genomic ancestry in Brazilians". Proceedings of the National Academy of Sciences of the United States of America. 100 (1): 177–182. Bibcode:2003PNAS..100..177P. doi:10.1073/pnas.0126614100. PMC 140919. PMID 12509516.
- ^ Telles, Edward Eric (2004). "Racial Classification". Race in Another America: The significance of skin color in Brazil. Princeton University Press. pp. 81–84. ISBN 0-691-11866-3.
- ^ Salek, Silvia (10 July 2007). "BBC delves into Brazilians' roots". BBC News. Retrieved 13 July 2009.
- ^ Ribeiro, Darcy (2008). O Povo Brasileiro [The Brazilian People] (in Portuguese) (4th reprint ed.). Companhia de Bolso.
- ^ Levine-Rasky, Cynthia, ed. (2002). Working through whiteness: international perspectives. SUNY Press. p. 73. ISBN 978-0-7914-5340-7.
'Money whitens' If any phrase encapsulates the association of whiteness and the modern in Latin America, this is it. It is a cliché formulated and reformulated throughout the region, a truism dependent upon the social experience that wealth is associated with whiteness, and that in obtaining the former one may become aligned with the latter (and vice versa).
- ^ a b Pena, Sérgio D. J.; Di Pietro, Giuliano; Fuchshuber-Moraes, Mateus; Genro, Julia Pasqualini; Hutz, Mara H.; Kehdy, Fernanda de Souza Gomes; Kohlrausch, Fabiana; Magno, Luiz Alexandre Viana; Montenegro, Raquel Carvalho; Moraes, Manoel Odorico; de Moraes, Maria Elisabete Amaral; de Moraes, Milene Raiol; Ojopi, Élida B.; Perini, Jamila A.; Racciopi, Clarice; Ribeiro-dos-Santos, Ândrea Kely Campos; Rios-Santos, Fabrício; Romano-Silva, Marco A.; Sortica, Vinicius A.; Suarez-Kurtz, Guilherme (2011). Harpending, Henry (ed.). "The Genomic Ancestry of Individuals from Different Geographical Regions of Brazil Is More Uniform Than Expected". PLoS One. 6 (2) e17063. Bibcode:2011PLoSO...617063P. doi:10.1371/journal.pone.0017063. PMC 3040205. PMID 21359226.
- ^ "Negros de origem européia" [Blacks of European origin]. afrobras.org.br (in Portuguese). Archived from the original on 24 November 2010.
- ^ Guerreiro-Junior, Vanderlei; Bisso-Machado, Rafael; Marrero, Andrea; Hünemeier, Tábita; Salzano, Francisco M.; Bortolini, Maria Cátira (2009). "Genetic signatures of parental contribution in black and white populations in Brazil". Genetics and Molecular Biology. 32 (1): 1–11. doi:10.1590/S1415-47572009005000001. PMC 3032968. PMID 21637639.
- ^ Pena, S. D. J.; Bastos-Rodrigues, L.; Pimenta, J. R.; Bydlowski, S. P. (2009). "Genetic heritage variability of Brazilians in even regional averages, 2009 study". Brazilian Journal of Medical and Biological Research. 42 (10): 870–876. doi:10.1590/S0100-879X2009005000026. PMID 19738982.
- ^ "Brasil: 500 anos de povoamento" [Brazil: 500 years of settlement] (in Portuguese). IBGE. Archived from the original on 23 September 2009. Retrieved 29 December 2011.
- ^ Ramos, Arthur (2003). A mestiçagem no Brasil [Miscegenation in Brazil] (in Portuguese). Maceió, Brazil: EDUFAL. p. 82. ISBN 978-85-7177-181-9.
- ^ De Assis Poiares, Lilian; De Sá Osorio, Paulo; Spanhol, Fábio Alexandre; Coltre, Sidnei César; Rodenbusch, Rodrigo; Gusmão, Leonor; Largura, Alvaro; Sandrini, Fabiano; Da Silva, Cláudia Maria Dornelles (2010). "Allele frequencies of 15 STRs in a representative sample of the Brazilian population" (PDF). Forensic Science International: Genetics. 4 (2): e61 – e63. doi:10.1016/j.fsigen.2009.05.006. PMID 20129458. Archived from the original (PDF) on 8 April 2011.
- ^ Oliveira Godinho, Neide Maria de (2008). O Impacto das Migrações na Constituição Genética de Populações Latino-Americanas [The Impact of Migration on the Genetic Constitution of Latin American Populations] (PDF) (PhD thesis) (in Portuguese). Universidade de Brasília. Archived from the original on 6 July 2011.
- ^ Lopes, Reinaldo José (5 October 2009). "DNA de brasileiro é 80% europeu, indica estudo" [Brazilian DNA is nearly 80% European, indicates study]. Folha de S.Paulo (in Portuguese).
- ^ Whitaker, Arthur P. (1984). Argentina. Hoboken, New Jersey: Prentice Hall., Cited in "Yale immigration study". Yale University.
- ^ Venâncio, Renato Pinto (2000). "Presença portuguesa: de colonizadores a imigrantes" [Portuguese presence: from colonizers to immigrants]. Brasil: 500 anos de povoamento [Brazil: 500 years of settlement]. Rio de Janeiro: IBGE., Relevant extract available here: "território brasileiro e povoamento" [Brazilian territory and settlement] (in Portuguese). IBGE. Retrieved 16 October 2021.
- ^ a b Council Directive 2000/43/EC of 29 June 2000 implementing the principle of equal treatment between persons irrespective of racial or ethnic origin
- ^ "European Union Directives on the Prohibition of Discrimination". HumanRights.is. Icelandic Human Rights Centre. Archived from the original on 24 July 2012.
- ^ a b Bell 2009, p. [page needed].
- ^ Sexton, Jared (2008). Amalgamation Schemes. University of Minnesota Press.
- ^ Nobles 2000
- ^ "Revisions to the Standards for the Classification of Federal Data on Race and Ethnicity". Office of Management and Budget. 30 October 1997. Archived from the original on 15 March 2009. Retrieved 19 March 2009. Also: U.S. Census Bureau Guidance on the Presentation and Comparison of Race and Hispanic Origin Data Archived 8 April 2019 at the Wayback Machine and B03002. Hispanic or Latino Origin by Race. 2007 American Community Survey 1-Year Estimates Archived 27 December 1996 at the Wayback Machine
- ^ Horsman, Reginald (1981). Race and Manifest Destiny: The Origins of American Radial Anglo-Saxonism. Cambridge, Massachusetts: Harvard University Press. p. 210., This reference is speaking in historic terms but there is not reason to think that this perception has altered much
- ^ Larsen, Clark Spencer, ed. (2010). A Companion to Biological Anthropology. Wiley-Blackwell. pp. 13, 26. ISBN 978-1-4051-8900-2.
'Race' as a typological characterization of human variation was to become a dominant theme in physical anthropology until the mid-twentieth century. ... Controversies over race did not end in the 1960s ... but there is a general sense in physical anthropology that the earlier use of race as a unit of study or as a conceptual unit is no longer viable and that this transition came in the 1960s.
- ^ a b Lieberman, Kirk & Corcoran 2003.
- ^ a b c Sauer 1992
- ^ Wagner, Jennifer K.; Yu, Joon-Ho; Ifekwunigwe, Jayne O.; Harrell, Tanya M.; Bamshad, Michael J.; Royal, Charmaine D. (February 2017). "Anthropologists' views on race, ancestry, and genetics". American Journal of Physical Anthropology. 162 (2): 318–327. Bibcode:2017AJPA..162..318W. doi:10.1002/ajpa.23120. PMC 5299519. PMID 27874171.
- ^ Štrkalj, Goran; Wang, Qian (2003). "On the Concept of Race in Chinese Biological Anthropology: Alive and Well" (PDF). Current Anthropology. 44 (3). University of Chicago Press: 403. doi:10.1086/374899. S2CID 224790805. Archived from the original (PDF) on 12 November 2013. Retrieved 12 November 2013.
- ^ Black & Ferguson 2011, p. 125.
- ^ Štrkalj, Goran (2007). "The Status of the Race Concept in Contemporary Biological Anthropology: A Review" (PDF). The Anthropologist. 9 (1): 73–78. doi:10.1080/09720073.2007.11890983. S2CID 13690181.
- ^ Kaszycka, Katarzyna A.; Štrkalj, Goran; Strzalko, Jan (2009). "Current Views of European Anthropologists on Race: Influence of Educational and Ideological Background". American Anthropologist. 111 (1): 43–56. doi:10.1111/j.1548-1433.2009.01076.x. S2CID 55419265.
- ^ Lieberman, Leonard; Kirk, Rodney C.; Littlefield, Alice (2003). "Perishing Paradigm: Race 1931–1999". American Anthropologist. 105 (1): 110–113. doi:10.1525/aa.2003.105.1.110.
An article in the same issue questions the precise rate of decline, but from their opposing perspective agrees that the Negroid/ Caucasoid/ Mongoloid paradigm has fallen into near-total disfavor.
^ Cartmill, Matt; Brown, Kaye (2003). "Surveying the Race Concept: A Reply to Lieberman, Kirk, and Littlefield". American Anthropologist. 105 (1): 114–115. doi:10.1525/aa.2003.105.1.114. - ^ AAA 1998
- ^ Bindon, Jim (2005). "Post World War II" (PDF). University of Alabama. Archived from the original (PDF) on 30 August 2006. Retrieved 28 August 2006.
- ^ Reynolds, Larry T.; Lieberman, Leonard (1996). Race and Other Misadventures: Essays in Honor of Ashley Montagu in His Ninetieth Year. Altamira Press. p. 159. ISBN 1-882-28935-8.
- ^ Lieberman 2001
- ^ Štrkalj, Goran (2007). "The Status of the Race Concept in Contemporary Biological Anthropology: A Review" (PDF). The Anthropologist. 9: 73–78. doi:10.1080/09720073.2007.11890983. S2CID 13690181.
- ^ a b Morning, Ann (November 2007). "'Everyone Knows It's a Social Construct': Contemporary Science and the Nature of Race". Sociological Focus. 40 (4): 436–454. doi:10.1080/00380237.2007.10571319. S2CID 145012814.
- ^ a b Gill 2000a.
- ^ Brace 2000a.
- ^ See:
- ^ Witzig 1996
- ^ a b Brace, C. Loring (1995). "Region Does not Mean 'Race': Reality Versus Convention in Forensic Anthropology". Journal of Forensic Sciences. 40 (2): 171–175. doi:10.1520/JFS15336J.
- ^ Hallinan, Christopher J. (March 1994). "The presentation of human biological diversity in sport and exercise science textbooks: The example of 'race'". Journal of Sport Behavior.
- ^ Rivara, Frederick P.; Finberg, Laurence (2001). "Use of the Terms Race and Ethnicity". Archives of Pediatrics & Adolescent Medicine. 155 (2): 119. doi:10.1001/archpedi.155.2.119. PMID 11177083.
In future issues of the Archives, we ask authors to not use race and ethnicity when there is no biological, scientific, or sociological reason for doing so. Race or ethnicity should not be used as explanatory variables, when the underlying constructs are variables that can, and should, be measured directly (eg, educational level of subjects, household income of the families, single vs 2-parent households, employment of parents, owning vs renting one's home, and other measures of socioeconomic status). In contrast, the recent attention on decreasing health disparities uses race and ethnicity not as explanatory variables but as ways of examining the underlying sociocultural reasons for these disparities and appropriately targeting attention and resources on children and adolescents with poorer health. In select issues and questions such as these, use of race and ethnicity is appropriate.
- ^ "Social and Demographic Studies of Rance and Ethnicity in the United States". Grants1.NIH.gov. US National Institutes of Health. 16 January 2003. PA-03-057. Archived from the original on 9 November 2014. Program announcement and request for grant applications (through 1 February 2006).
- ^ Schwartz, Robert S. (3 May 2001). "Racial Profiling in Medical Research". The New England Journal of Medicine. 344 (18): 1392–1393. doi:10.1056/NEJM200105033441810. PMID 11333999.
- ^ Morning, Ann (2008). "Reconstructing Race in Science and Society: Biology Textbooks, 1952–2002". American Journal of Sociology. 114 (114 Suppl): S106 – S137. doi:10.1086/592206. PMID 19569402. S2CID 13552528.
- ^ Gissis, S. (2008). "When is 'race' a race? 1946–2003". Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences. 39 (4): 437–450. doi:10.1016/j.shpsc.2008.09.006. PMID 19026975.
- ^ Moscou, Susan (June 2008). "The conceptualization and operationalization of race and ethnicity by health services researchers". Nursing Inquiry. 15 (2): 94–105. doi:10.1111/j.1440-1800.2008.00413.x. PMID 18476852.
- ^ Štrkalj, Goran; Solyali, Veli (2010). "Human Biological Variation in Anatomy Textbooks: The Role of Ancestry". Studies on Ethno-Medicine. 4 (3). Kamla-Raj Ent.: 157–161. doi:10.1080/09735070.2010.11886375. S2CID 73945508.
- ^ "Geneticists curb use of 'race'". Science. 374 (6572): 1177. 3 December 2021.
- ^ a b "Researchers Need to Rethink and Justify How and Why Race, Ethnicity, and Ancestry Labels Are Used in Genetics and Genomics Research, Says New Report". National Academies. 14 March 2023. Retrieved 17 April 2023.
- ^ Kaiser, Jocelyn (14 March 2023). "Geneticists should rethink how they use race and ethnicity, panel urges". Science. Online. doi:10.1126/science.adh7982.
- ^ a b c d Frazier, E. Franklin (1947). "Sociological Theory and Race Relations". American Sociological Review. 12 (3): 265–271. doi:10.2307/2086515. JSTOR 2086515.
- ^ a b c Appelrouth, Scott; Edles, Laura Desfor (2016). Classical and Contemporary Sociological Theory. Thousand Oaks, California: Sage Publishing. ISBN 978-1-4522-0362-1.
- ^ Cooley, Charles H. (May 1897). "Genius, Fame and the Comparison of Races". Annals of the American Academy of Political and Social Science. 9 (3): 1–42. doi:10.1177/000271629700900301. hdl:2027.42/66770. S2CID 144674315 – via Brock University. Republished as: Jacoby, Russell; Glauberman, Naomi, eds. (1995). "Genius, Fame, and Race". The Bell Curve Debate: History, Documents, Opinions. Toronto: Random House. pp. 417–437.
- ^ a b c Fitzgerald, Kathleen J. (2014). Recognizing Race and Ethnicity: Power, Privilege, and Inequality. Boulder, Colorado: Westview Press.
- ^ Wilson, William Julius (1978). "The Declining Significance of Race: Blacks and Changing American Institutions". In Grusky, David B. (ed.). Social Stratification: Class, Race, and Gender in Sociological Perspective. Boulder, Colorado: Westview Press. pp. 765–776.
- ^ a b Omi, Michael; Winant, Howard (2014). "Racial Formation in the United States". In Grusky, David B . (ed.). Social Stratification: Class, Race, and Gender in Sociological Perspective (4th ed.). Boulder, Colorado: Westview Press. p. 683. ISBN 978-0-8133-4671-7.
- ^ Rothenberg, P. S. Race, Class, and Gender in the United States (text only) (7th ed.). p. 131.
- ^ a b Bonilla-Silva, Eduardo (2006). Racism Without Racists (2nd ed.). Rowman and Littlefield.
- ^ "Office of Minority Health". Minorityhealth.hhs.gov. 16 August 2011. Archived from the original on 18 January 2013. Retrieved 30 December 2012.
- ^ Risch et al. 2002
- ^ a b Condit, Celeste; Templeton, Alan; Bates, Benjamin R.; Bevan, Jennifer L.; Harris, Tina M. (September 2003). "Attitudinal barriers to delivery of race-targeted pharmacogenomics among informed lay persons". Genetics in Medicine. 5 (5): 385–392. doi:10.1097/01.GIM.0000087990.30961.72. PMID 14501834. In summary, they argues that, in order to predict the clinical success of pharmacogenomic research, scholars must conduct subsidiary research on two fronts: Science, wherein the degree of correspondence between popular and professional racial categories can be assessed; and society at large, through which attitudinal factors moderate the relationship between scientific soundness and societal acceptance. To accept race-as-proxy, then, may be necessary but insufficient to solidify the future of race-based pharmacogenomics.
- ^ Lee, Catherine (March 2009). "'Race' and 'ethnicity' in biomedical research: How do scientists construct and explain differences in health?". Social Science & Medicine. 68 (6): 1183–1190. doi:10.1016/j.socscimed.2008.12.036. PMID 19185964.
- ^ Graves 2011
- ^ Fullwiley 2011
- ^ Harpending 2006, p. 458 "On the other hand, information about the race of patients will be useless as soon as we discover and can type cheaply the underlying genes that are responsible for the associations. Can races be enumerated in any unambiguous way? Of course not, and this is well known not only to scientists but also to anyone on the street."
- ^ Lee et al. 2008
- ^ Kahn 2011, p. 132. "For example, what are we to make of the fact that African Americans suffer from disproportionately high rates of hypertension, but Africans in Nigeria have among the world's lowest rates of hypertension, far lower than the overwhelmingly white population of Germany? Genetics certainly plays a role in hypertension. But any role it plays in explaining such differences must surely be vanishingly small." Citing: Cooper, Richard; Wolf-Maier, Katharina; Luke, Amy; Adeyemo, Adebowale; Banegas, José R.; Forrester, Terrence; Giampaoli, Simona; Joffres, Michel; Kastarinen, Mika; Primatesta, Paola; Stegmayr, Birgitta; Thamm, Michael (5 January 2005). "An International Comparative Study of Blood Pressure in Populations of European vs. African Descent". BMC Medicine. 3 (2): 2. doi:10.1186/1741-7015-3-2. PMC 545060. PMID 15629061.
- ^ "Statistics on Race and the Criminal Justice System 2010, Appendix C: Classifications of ethnicity" (PDF). Ministry of Justice. October 2011. Retrieved 24 September 2014.
- ^ "Stop and Search Manual". Suffolk Constabulary Policies & Procedures. Archived from the original on 26 August 2014. Retrieved 24 September 2014.
- ^ "Office of National Statistics: Review of equality data: audit report" Archived 26 August 2014 at the Wayback Machine Retrieved 24 September 2014.
- ^ Bleich, Erik (1 May 2001). "Race Policy in France". The Brookings Institution.
- ^ "Race | Boundless Sociology". courses.lumenlearning.com. Retrieved 6 July 2019.
- ^ Alexander 2010, p. 13.
- ^ Alexander 2010, p. 12.
- ^ Dichter, M. E.; Marcus, S. M.; Morabito, M. S.; Rhodes, K. V. (2011). "Explaining the IPV arrest decision: Incident, agency, and community factors". Criminal Justice Review. 36: 22–39. doi:10.1177/0734016810383333. S2CID 146748135.
- ^ Abraham 2009
- ^ Willing 2005
- ^ Kennedy 1995
- ^ Konigsberg, Lyle W.; Algee-Hewitt, Bridget F. B.; Steadman, Dawnie Wolfe (1 May 2009). "Estimation and evidence in forensic anthropology: Sex and race". American Journal of Physical Anthropology. 139 (1): 77–90. Bibcode:2009AJPA..139...77K. doi:10.1002/ajpa.20934. ISSN 1096-8644. PMID 19226642.
- ^ "Does Race Exist?". www.pbs.org. 15 February 2000. Retrieved 9 November 2017.
- ^ Relethford, John H. (11 July 2002). "Apportionment of global human genetic diversity based on craniometrics and skin color" (PDF). American Journal of Physical Anthropology. 118 (4): 393–398. Bibcode:2002AJPA..118..393R. doi:10.1002/ajpa.10079. PMID 12124919. S2CID 8717358. Archived from the original (PDF) on 26 October 2017. Retrieved 25 October 2017.
- ^ Relethford, John H. (18 February 2009). "Race and global patterns of phenotypic variation". American Journal of Physical Anthropology. 139 (1): 16–22. Bibcode:2009AJPA..139...16R. doi:10.1002/ajpa.20900. PMID 19226639.
Craniometric variation is geographically structured, allowing high levels of classification accuracy when comparing crania from different parts of the world. Nonetheless, the boundaries in global variation are not abrupt and do not fit a strict view of the race concept; the number of races and the cutoffs used to define them are arbitrary.
- ^ Ousley, Jantz & Freid 2009
- ^ Sesardic 2010
- ^ Pigliucci 2013
Bibliography
[edit]- Abraham, Carolyn (7 April 2009). "Molecular eyewitness: DNA gets a human face". The Globe and Mail. Archived from the original on 17 July 2011. Retrieved 4 February 2011.
- "American Anthropological Association Statement on 'Race'". AAAnet.org. American Anthropological Association. 17 May 1998. Retrieved 18 April 2009.
- "AAPA statement on biological aspects of race" (PDF). American Journal of Physical Anthropology. 101 (4). American Association of Physical Anthropologists: 569–570. 1996. Bibcode:1996AJPA..101..569.. doi:10.1002/ajpa.1331010408. Archived from the original (PDF) on 23 July 2004.
- Alexander, Michelle (2010). The New Jim Crow: Mass Incarceration in the Age of Colorblindness. New York: The New Press.
- Amundson, Ron (2005). "Disability, Ideology, and Quality of Life: A Bias in Biomedical Ethics". In Wasserman, David T.; Wachbroit, Robert Samuel; Bickenbach, Jerome Edmund (eds.). Quality of life and human difference: genetic testing, health care, and disability. Cambridge University Press. pp. 101–124. ISBN 978-0-521-83201-4.
- Andreasen, Robin O. (2000). "Race: Biological Reality or Social Construct?". Philosophy of Science. 67 (Supplement): S653 – S666. doi:10.1086/392853. JSTOR 188702. S2CID 144176104.
- Angier, Natalie (22 August 2000). "Do Races Differ? Not Really, DNA Shows". The New York Times. Retrieved 9 August 2010.
- Appiah, Kwame Anthony (1992). In My Father's House: Africa in the Philosophy of Culture. Oxford University Press. ISBN 978-0-19-506852-8.
- Armelagos, George; Smay, Diana (2000). "Galileo wept: A critical assessment of the use of race in forensic anthropology" (PDF). Transforming Anthropology. 9 (2): 19–29. doi:10.1525/tran.2000.9.2.19. S2CID 143942539. Archived from the original (PDF) on 18 August 2018. Retrieved 15 May 2010.
- Bamshad, Michael; Olson, Steve E. (10 November 2003). "Does Race Exist?" (PDF). Scientific American. Vol. 289, no. 6. pp. 78–85. Bibcode:2003SciAm.289f..78B. doi:10.1038/scientificamerican1203-78. PMID 14631734. Archived from the original (PDF) on 14 June 2007.
- Bamshad, M.; Wooding, S.; Salisbury, B. A.; Stephens, J. C. (August 2004). "Deconstructing the relationship between genetics and race". Nature Reviews Genetics. 5 (8): 598–609. doi:10.1038/nrg1401. PMID 15266342. S2CID 12378279.
- Banton, Michael (1977). The idea of race (paperback). Boulder, Colorado: Westview Press. ISBN 0-89158-719-5.
- Barbujani, Guido (1 June 2005). "Human Races: Classifying People vs Understanding Diversity". Current Genomics. 6 (4): 215–226. doi:10.2174/1389202054395973. S2CID 18992187.
- Bell, Mark (2009). "'Race', Ethnicity, and Racism in Europe" (PDF). Racism and Equality in the European Union. Oxford University Press. doi:10.1093/acprof:oso/9780199297849.001.0001. ISBN 978-0-19-929784-9. Archived from the original (PDF) on 2 December 2012.
- Black, Sue; Ferguson, Elidh (2011). Forensic Anthropology: 2000 to 2010. Taylor & Francis. ISBN 978-1-439-84588-2.
- Blank, Rebecca M.; Dabady, Marilyn; Citro, Constance Forbes (2004). "Chapter 2". Measuring racial discrimination. National Research Council (U.S.) Panel on Methods for Assessing Discrimination. National Adademies Press. p. 317. ISBN 978-0-309-09126-8.
- Bloche, Gregg M. (2004). "Race-Based Therapeutics". New England Journal of Medicine. 351 (20): 2035–2037. doi:10.1056/NEJMp048271. PMID 15533852. S2CID 1467851.
- Boas, Franz (1912). "Change in Bodily Form of Descendants of Immigrants". American Anthropologist. 14 (3): 530–562. doi:10.1525/aa.1912.14.3.02a00080. PMC 2986913.
- Boyd, William C. (1950). Genetics and the races of man: an introduction to modern physical anthropology. Boston: Little, Brown and Company. p. 207.
- Brace, C. Loring; Montagu, Ashley (1965). Man's Evolution: An Introduction to Physical Anthropology. New York: Macmillan.
- Brace, C. Loring (2000). Evolution in an Anthropological View. Rowman & Littlefield. ISBN 978-0-7425-0263-5.
- Brace, C. Loring (2000a). "Does Race Exist? An antagonist's perspective". Nova. PBS. Retrieved 11 October 2010.
- Brace, C. Loring (2005). Race is a four letter word. Oxford University Press. ISBN 978-0-19-517351-2.
- Caspari, Rachel (March 2003). "From types to populations: A century of race, physical anthropology, and the American Anthropological Association". American Anthropologist. 105 (1): 65–76. doi:10.1525/aa.2003.105.1.65. hdl:2027.42/65890.
- Cavalli-Sforza, Luigi Luca; Menozzi, Paolo; Piazza, Alberto (1994). The History and Geography of Human Genes. Princeton University Press. ISBN 978-0-691-08750-4. Lay summary Archived 2 February 2022 at the Wayback Machine (1 December 2013)
- Conley, D. (2007). "Being black, living in the red"". In Rothenberg, P. S. (ed.). Race, Class, and Gender in the United States (7th ed.). New York: Worth Publishers. pp. 350–358.
- Cravens, Hamilton (2010). "What's New in Science and Race since the 1930s?: Anthropologists and Racial Essentialism". The Historian. 72 (2): 299–320. doi:10.1111/j.1540-6563.2010.00263.x. PMID 20726131. S2CID 10378582.
- Crenshaw KW (1988). "Race, reform, and retrenchment: Transformation and legitimation in antidiscrimination law". Harvard Law Review. 101 (7): 1331–1337. doi:10.2307/1341398. JSTOR 1341398.
- Currell, Susan; Cogdell, Christina (2006). Popular Eugenics: National Efficiency and American Mass Culture in The 1930s. Athens, Ohio: Ohio University Press. p. 203. ISBN 0-8214-1691-X.
- Desmond, Adrian; Moore, James (2009), Darwin's sacred cause: how a hatred of slavery shaped Darwin's views on human evolution, Allen Lane, Penguin Books, p. 484, ISBN 978-1-84614-035-8
- Dikötter, Frank (1992). The discourse of race in modern China. Stanford University Press. ISBN 978-0-8047-1994-0.
- Edwards, A. W. F. (August 2003). "Human genetic diversity: Lewontin's fallacy". BioEssays. 25 (8): 798–801. doi:10.1002/bies.10315. PMID 12879450. S2CID 17361449.
- Ehrlich, Paul; Holm, Richard W. (1964). "A Biological View of Race". In Montagu, Ashley (ed.). The Concept of Race. Collier Books. pp. 153–179.
- Fullwiley, Duana (2011). "Chapter 6: Can DNA "Witness" Race?". In Krimsky, Sheldon; Sloan, Kathleen (eds.). Race and the Genetic Revolution: Science, Myth, and Culture. Columbia University Press. ISBN 978-0-231-52769-9. Retrieved 31 August 2013.
- Gill, G. W. (2000a). "Does Race Exist? A proponent's perspective". NOVA. PBS. Retrieved 18 April 2009.
- Gitschier, Jane (2005). "The Whole Side of It – An Interview with Neil Risch". PLOS Genetics. 1 (1) e14. doi:10.1371/journal.pgen.0010014. PMC 1183530. PMID 17411332.
- Gordon, Milton Myron (1964). Assimilation in American life: the role of race, religion, and national origins. Oxford University Press. ISBN 978-0-19-500896-8.
{{cite book}}: ISBN / Date incompatibility (help) - Graves, Joseph L. (2001). The Emperor's New Clothes: Biological Theories of Race at the Millennium. Rutgers University Press. ISBN 978-0-8135-2847-2.
- Graves, Joseph L. (2011). "Chapter 8: Evolutionary Versus Racial Medicine". In Krimsky, Sheldon; Sloan, Kathleen (eds.). Race and the Genetic Revolution: Science, Myth, and Culture. Columbia University Press. ISBN 978-0-231-52769-9. Retrieved 31 August 2013.
- Haig, S. M.; Beever, E. A.; Chambers, S. M.; Draheim, H. M.; et al. (December 2006). "Taxonomic considerations in listing subspecies under the U.S. Endangered Species Act". Conservation Biology. 20 (6): 1584–1594. Bibcode:2006ConBi..20.1584H. doi:10.1111/j.1523-1739.2006.00530.x. PMID 17181793. S2CID 9745612.
- Harpending, Henry (2006). "Chapter 16: Anthropological Genetics: Present and Future". In Crawford, Michael (ed.). Anthropological Genetics: Theory, Methods and Applications. Cambridge University Press. ISBN 978-0-521-54697-3.
- Harris, Marvin (1980). Patterns of race in the Americas. Westport, Connecticut: Greenwood Press. ISBN 0-313-22359-9.
- Human Genome Project (2003). "Human Genome Project Information: Minorities, Race, and Genomics". Human Genome Program, US Department of Energy. Archived from the original on 15 May 2009. Retrieved 20 November 2011.
- Kahn, Jonathan (2011). "Chapter 7: Bidil and Racialized Medicine". In Krimsky, Sheldon; Sloan, Kathleen (eds.). Race and the Genetic Revolution: Science, Myth, and Culture. Columbia University Press. p. 132. ISBN 978-0-231-52769-9. Retrieved 31 August 2013.
- Kaplan, J. M.; Winther, R. G. (2013). "Prisoners of Abstraction? The Theory and Measure of Genetic Variation, and the Very Concept of 'Race'" (PDF). Biological Theory. 7 (4): 401–412. doi:10.1007/s13752-012-0048-0.
- Keita, S. O. Y.; Kittles, R. A.; Royal, C. D. M.; Bonney, G. M.; Furbert-Harris, P.; Dunston, G. M.; Rotimi, C. M. (2004). "Conceptualizing human variation". Nature Genetics. 36 (11s): S17 – S20. doi:10.1038/ng1455. PMID 15507998.
- Kennedy, Kenneth A. R. (1995). "But Professor, Why Teach Race Identification if Races Don't Exist?". Journal of Forensic Sciences. 40 (5) 15386J. doi:10.1520/jfs15386j.
- King, Desmond (2007). "Making people work: Democratic consequences of workfare". In Beem, Christopher; Mead, Lawrence M. (eds.). Welfare Reform and Political Theory. New York: Russell Sage Foundation Publications. pp. 65–81. ISBN 978-0-87154-588-6.
- Lee, Jayne Chong-Soon (1997). "Review essay: Navigating the topology of race". In Gates, E. Nathaniel (ed.). Critical Race Theory: Essays on the Social Construction and Reproduction of Race. Vol. 4: The Judicial Isolation of the "Racially" Oppressed. New York: Garland Pub. pp. 393–426. ISBN 978-0-8153-2603-8.
- Lee, Sandra S. J.; Mountain, Joanna; Koenig, Barbara; Altman, Russ (2008). "The ethics of characterizing difference: guiding principles on using racial categories in human genetics". Genome Biology. 9 (7): 404. doi:10.1186/gb-2008-9-7-404. PMC 2530857. PMID 18638359.
- Lewis, Bernard (1990). Race and Slavery in the Middle East: An Historical Enquiry. New York: Oxford University Press. ISBN 0-19-506283-3.
- Lie, John (2004). Modern Peoplehood. Cambridge, Massachusetts: Harvard University Press. ISBN 0-674-01327-1.
- Lieberman, L. (February 2001). "How 'Caucasoids' got such big crania and why they shrank: from Morton to Rushton". Current Anthropology. 42 (1): 69–95. doi:10.1086/318434. PMID 14992214. S2CID 224794908.
- Lieberman, Leonard; Kirk, Rodney (1997). "Teaching About Human Variation: An Anthropological Tradition for the Twenty-first Century". In Rice, Patricia; Kottak, Conrad Phillip; White, Jane G.; Furlow, Richard H. (eds.). The Teaching of Anthropology: Problems, Issues, and Decisions. Mayfield Pub. p. 381. ISBN 1-55934-711-2.
- Lieberman, L.; Kirk, R. C.; Corcoran, M. (2003). "The decline of race in American physical anthropology" (PDF). Anthropological Review. 66: 3–21. ISSN 0033-2003. Archived from the original (PDF) on 13 August 2012.
- Lieberman, Leonard; Jackson, Fatimah Linda C. (1995). "Race and Three Models of Human Origins". American Anthropologist. 97 (2): 231–242. doi:10.1525/aa.1995.97.2.02a00030. S2CID 53473388.
- Lieberman, Leonard; Hampton, Raymond E.; Littlefield, Alice; Hallead, Glen (1992). "Race in Biology and Anthropology: A Study of College Texts and Professors". Journal of Research in Science Teaching. 29 (3): 301–321. Bibcode:1992JRScT..29..301L. doi:10.1002/tea.3660290308.
- Lewontin, Richard C. (1972). "The Apportionment of Human Diversity". Evolutionary Biology. Vol. 6. pp. 381–397. doi:10.1007/978-1-4684-9063-3_14. ISBN 978-1-4684-9065-7. S2CID 21095796.
- Livingstone, Frank B.; Dobzhansky, Theodosius (1962). "On the Non-Existence of Human Races". Current Anthropology. 3 (3): 279–281. doi:10.1086/200290. JSTOR 2739576. S2CID 144257594.
- Long, J. C.; Kittles, R. A. (August 2003). "Human genetic diversity and the nonexistence of biological races". Human Biology. 75 (4): 449–71. doi:10.1353/hub.2003.0058. PMID 14655871. S2CID 26108602.
- Long, Jeffrey C. (2009). "Update to Long and Kittles's 'Human Genetic Diversity and the Nonexistence of Biological Races' (2003): Fixation on an Index". Human Biology. 81 (5/6): 799–803. doi:10.3378/027.081.0622. JSTOR 41466642. PMID 20504197. S2CID 4385409.
- Marks, J. (1995). Human biodiversity: Genes, race, and history. New York: Aldine de Gruyter. ISBN 0-585-39559-4.
- Marks, Jonathan (2002). "Folk Heredity". In Fish, Jefferson M. (ed.). Race and Intelligence: Separating Science from Myth. Mahwah, New Jersey: Lawrence Erlbaum Associates. p. 98. ISBN 0-8058-3757-4.
- Marks, Jonathan (2008). "Race: Past, present and future. Chapter 1". In Koenig, Barbara; Soo-Jin Lee, Sandra; Richardson, Sarah S. (eds.). Revisiting Race in a Genomic Age. Rutgers University Press.
- McNeilly, M. D.; Anderson, M. B.; Armstead, C. A.; Clark, R.; Corbett, M.; Robinson, E. L. (1996). "The perceived racism scale: A multidimensional assessment of the experience of white racism among African Americans". Ethnicity & Disease. 6 (1–2): 154–166.
- Meltzer, Milton (1993). Slavery: a world history (revised ed.). Cambridge, Massachusetts: DaCapo Press. ISBN 0-306-80536-7.
- Mevorach, Katya Gibel (2007). "Race, racism, and academic complicity". American Ethnologist. 34 (2): 238–241. doi:10.1525/ae.2007.34.2.238.
- Miles, Robert (2000). "Apropos the idea of race ... again". In Back, Les; Solomos, John (eds.). Theories of race and racism. Psychology Press. pp. 125–143. ISBN 978-0-415-15672-1.
- Molnar, Stephen (1992). Human variation: races, types, and ethnic groups. Englewood Cliffs, New Jersey: Prentice Hall. ISBN 0-13-446162-2.
- Montagu, Ashley (1941). "The Concept of Race in the Human Species in the Light of Genetics". Journal of Heredity. 32 (8): 243–248. doi:10.1093/oxfordjournals.jhered.a105051.
- Montagu, Ashley (1997) [1942]. Man's Most Dangerous Myth: The Fallacy of Race (paperback). AltaMira Press. ISBN 0-8039-4648-1.
- Montagu, Ashley (1962). "The Concept of Race". American Ethnography Quasiweekly. Archived from the original on 3 June 2011. Retrieved 26 January 2009. Originally appeared in: Montagu, Ashley (October 1962). "The Concept of Race". American Anthropologist. New Series. 64 (5:1): 919–928. doi:10.1525/aa.1962.64.5.02a00020.
- Morgan, Edmund S. (1975). American Slavery, American Freedom: The Ordeal of Colonial Virginia. W. W. Norton and Company, Inc.
- Mountain, Joanna L.; Risch, Neil (2004). "Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groups". Nature Genetics. 36 (11 Suppl): S48 – S53. doi:10.1038/ng1456. PMID 15508003. S2CID 8136003.
- Muffoletto, Robert (2003). "Ethics: A discourse of power". TechTrends. 47 (6): 62–66. doi:10.1007/BF02763286. S2CID 144150827.
- Nobles, Melissa (2000). Shades of citizenship: race and the census in modern politics. Stanford University Press. ISBN 0-8047-4059-3.
- Ossorio, P.; Duster, T. (2005). "Controversies in biomedical, behavioral, and forensic sciences". American Psychologist. 60 (1): 115–128. doi:10.1037/0003-066X.60.1.115. PMID 15641926.
- Ousley, Stephen; Jantz, Richard; Freid, Donna (18 February 2009). "Understanding race and human variation: Why forensic anthropologists are good at identifying race". American Journal of Physical Anthropology. 139 (1): 68–76. Bibcode:2009AJPA..139...68O. doi:10.1002/ajpa.21006. PMID 19226647. S2CID 24410231.
- Owens, K.; King, M. C. (1999). "Genomic Views of Human History". Science. 286 (5439): 451–453. doi:10.1126/science.286.5439.451. PMID 10521333.
- Palmié, Stephan (May 2007). "Genomics, divination, 'racecraft'". American Ethnologist. 34 (2): 205–222. doi:10.1525/ae.2007.34.2.205.
- Pigliucci, Massimo (September 2013). "What are we to make of the concept of race?". Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences. 44 (3): 272–277. doi:10.1016/j.shpsc.2013.04.008. PMID 23688802.
- Reardon, Jenny (2005). "Post World-War II Expert Discourses on Race". Race to the finish: identity and governance in an age of genomics. Princeton University Press. pp. 17ff. ISBN 978-0-691-11857-4.
- Risch, N.; Burchard, E.; Ziv, E.; Tang, H. (July 2002). "Categorization of humans in biomedical research: genes, race and disease". Genome Biology. 3 (7). comment2007. doi:10.1186/gb-2002-3-7-comment2007. PMC 139378. PMID 12184798.
- Rosenberg, N. A.; Mahajan, S.; Ramachandran, S.; Zhao, C.; Pritchard, J. K.; Feldman, M. W. (2005). "Clines, Clusters, and the Effect of Study Design on the Inference of Human Population Structure". PLOS Genetics. 1 (6) e70. doi:10.1371/journal.pgen.0010070. PMC 1310579. PMID 16355252.
- Sauer, Norman J. (January 1992). "Forensic Anthropology and the Concept of Race: If Races Don't Exist, Why are Forensic Anthropologists So Good at Identifying them". Social Science and Medicine. 34 (2): 107–111. doi:10.1016/0277-9536(92)90086-6. ISSN 0277-9536. PMID 1738862.
- Sesardic, Neven (2010). "Race: A Social Destruction of a Biological Concept". Biology & Philosophy. 25 (143): 143–162. doi:10.1007/s10539-009-9193-7. S2CID 3013094.
- Segal, Daniel A. (1991). "'The European': Allegories of Racial Purity". Anthropology Today. 7 (5). Royal Anthropological Institute of Great Britain and Ireland: 7–9. doi:10.2307/3032780. JSTOR 3032780.
- Serre, D.; Pääbo, S. (September 2004). "Evidence for gradients of human genetic diversity within and among continents". Genome Research. 14 (9): 1679–85. doi:10.1101/gr.2529604. PMC 515312. PMID 15342553.
- Schaefer, Richard T., ed. (2008). Encyclopedia of Race, Ethnicity and Society. SAGE Publishing. p. 1096. ISBN 978-1-4129-2694-2.
- Sivanandan, Ambalavaner (1982). A Different Hunger: Writings on Black Resistance. Pluto Press. ISBN 978-0-86104-371-2.
- Slotkin, J. S. (1965). "The Eighteenth Century". Readings in early Anthropology. Methuen Publishing. pp. 175–243.
- Smaje, Chris (1997). "Not just a social construct: Theorising race and ethnicity". Sociology. 31 (2): 307–327. doi:10.1177/0038038597031002007. S2CID 145703746.
- Smedley, A. (1999). Race in North America: origin and evolution of a worldview (2nd ed.). Boulder, Colorado: Westview Press. ISBN 0-8133-3448-9.
- Smedley, Audrey (2002). "Science and the Idea of Race: A Brief History". In Fish, Jefferson M. (ed.). Race and Intelligence: Separating Science from Myth. Mahwah, New Jersey: Lawrence Erlbaum Associates. p. 172. ISBN 0-8058-3757-4.
- Smedley, Audrey (2007). The History of the Idea of Race... and Why It Matters (PDF). Race, Human Variation and Disease: Consensus and Frontiers, March 14–17, 2007 in Warrenton, Virginia. American Anthropological Association. Archived from the original (PDF) on 13 November 2019. Retrieved 21 January 2011.
- Sober, Elliott (2000). Philosophy of biology (2nd ed.). Boulder, Colorado: Westview Press. ISBN 978-0-8133-9126-7.
- Stocking, George W. (1968). Race, Culture and Evolution: Essays in the History of Anthropology. University of Chicago Press. p. 380. ISBN 978-0-226-77494-7.
- Takaki, R. (1993). A different mirror: a history of multicultural America (paperback). Boston: Little, Brown. ISBN 0-316-83112-3.
- Tang, Hua; Quertermous, Tom; Rodriguez, Beatriz; Kardia, Sharon L. R.; Zhu, Xiaofeng; Brown, Andrew; Pankow, James S.; Province, Michael A.; Hunt, Steven C.; Boerwinkle, Eric; Schork, Nicholas J.; Risch, Neil J. (2005). "Genetic Structure, Self-identified Race/Ethnicity, and Confounding in Case-control Association Studies". The American Journal of Human Genetics. 76 (2): 268–275. doi:10.1086/427888. PMC 1196372. PMID 15625622.
- Templeton, Alan R. (1998). "Human Races: A Genetic and Evolutionary Perspective". American Anthropologist. 100 (3): 632–650. doi:10.1525/aa.1998.100.3.632. ISSN 0002-7294. JSTOR 682042.
- Templeton, Alan R. (2002). "The genetic and evolutionary significance of human races". In Fish, J. M. (ed.). Race and Intelligence: Separating Science from Myth. Mahwah, New Jersey: Lawrence Erlbaum Associates.
- Templeton, Alan R. (September 2013). "Biological Races in Humans". Studies in History and Philosophy of Biological and Biomedical Sciences. 44 (3): 262–271. doi:10.1016/j.shpsc.2013.04.010. ISSN 1369-8486. PMC 3737365. PMID 23684745.
- Thompson, William; Hickey, Joseph (2005). Society in Focus. Boston: Pearson. ISBN 0-205-41365-X.
- Todorov, T. (1993). On human diversity. Cambridge, Massachusetts: Harvard University Press. ISBN 0-674-63438-1.
- Weiss, Rick (16 December 2005). "Scientists Find a DNA Change That Accounts for Light Skin". The Washington Post.
- Willing, Richard (16 August 2005). "DNA tests offer clues to suspect's race". USA Today.
- Wilson, E. O.; Brown, W. L. (1953). "The Subspecies Concept and Its Taxonomic Application". Systematic Zoology. 2 (3): 97–110. doi:10.2307/2411818. JSTOR 2411818.
- Winfield, A. G. (2007). Eugenics and education in America: Institutionalized racism and the implications of history, ideology, and memory. New York: Peter Lang Publishing, Inc. pp. 45–46.
- Witherspoon, D. J.; Wooding, S.; Rogers, A. R.; Marchani, E. E.; Watkins, W. S.; Batzer, M. A.; Jorde, L. B. (2007). "Genetic Similarities Within and Between Human Populations". Genetics. 176 (1): 351–359. doi:10.1534/genetics.106.067355. PMC 1893020. PMID 17339205.
- Witzig, R. (15 October 1996). "The medicalization of race: scientific legitimization of a flawed social construct". Annals of Internal Medicine. 125 (8): 675–679. doi:10.7326/0003-4819-125-8-199610150-00008. PMID 8849153. S2CID 41786914.
- Wright, Sewall (1978). Evolution and the Genetics of Populations. Vol. 4: Variability Within and Among Natural Populations. Chicago: Univ. Chicago Press. p. 438.
- Xing, Jinchuan; Watkins, W. Scott; Shlien, Adam; Walker, Erin; Huff, Chad D.; Witherspoon, David J.; Zhang, Yuhua; Simonson, Tatum S.; Weiss, Robert B.; Schiffman, Joshua D.; Malkin, David; Woodward, Scott R.; Jorde, Lynn B. (2010). "Toward a more uniform sampling of human genetic diversity: A survey of worldwide populations by high-density genotyping". Genomics. 96 (4): 199–210. doi:10.1016/j.ygeno.2010.07.004. ISSN 0888-7543. PMC 2945611. PMID 20643205.
Further reading
[edit]- Amadon, D. (1949). "The seventy-five percent rule for subspecies". Condor. 51 (6): 250–258. doi:10.2307/1364805. JSTOR 1364805. S2CID 87016263.
- Anderson, N. B.; Bulatao, R. A.; Cohen, B. (2004). Critical Perspectives on Racial and Ethnic Differences in Health in Late Life: 2. Racial and Ethnic Identification, Official Classifications, and Health Disparities. National Academies Press. ISBN 0-309-09211-6.
- Anemone, Robert L. (2011). Race and Human Diversity: A Biocultural Approach. Upper Saddle River, New Jersey: Prentice Hall. ISBN 978-0-131-83876-5.
- Cartmill, Matt (1998). "The status of the race concept in physical anthropology" (PDF). American Anthropologist. 100 (3). American Anthropological Association: 651–660. doi:10.1525/aa.1998.100.3.651. Archived from the original (PDF) on 17 May 2017. Retrieved 26 June 2015.
- Coop, G.; Pickrell, J. K.; Novembre, J.; Kudaravalli, S.; Li, J. (2009). "The Role of Geography in Human Adaptation". PLOS Genetics. 5 (6) e1000500. doi:10.1371/journal.pgen.1000500. PMC 2685456. PMID 19503611.
- Cooper, R. S.; Kaufman, J. S.; Ward, R. (2003). "Race and genomics". New England Journal of Medicine. 348 (12): 1166–1170. doi:10.1056/NEJMsb022863. PMID 12646675. S2CID 11095726.
- Davenport, Lauren (May 2020). "The Fluidity of Racial Classifications". Annual Review of Political Science. 23: 221–240. doi:10.1146/annurev-polisci-060418-042801. S2CID 212962606.
- Dobzhansky, T. (1970). Genetics of the Evolutionary Process. New York: Columbia University Press. ISBN 0-231-02837-7.
- Duster, T. (2005). "Race and reification in science". Science. 307 (5712): 1050–1051. doi:10.1126/science.1110303. PMID 15718453. S2CID 28235427.
- Graves, Joseph L. (2006). "What We Know and What We Don't Know: Human Genetic Variation and the Social Construction of Race". Is Race "Real"?. Social Science Research Council. Retrieved 22 January 2011.
- Hawks, John (2013). "Significance of Neandertal and Denisovan Genomes in Human Evolution". Annual Review of Anthropology. 42 (1). Annual Reviews: 433–449. doi:10.1146/annurev-anthro-092412-155548. ISBN 978-0-8243-1942-7. ISSN 0084-6570.
- Helms, Janet E.; Jernigan, Maryam; Mascher, Jackquelyn (2005). "The meaning of race in psychology and how to change it: A methodological perspective". American Psychologist. 60 (1): 27–36. doi:10.1037/0003-066X.60.1.27. PMID 15641919. S2CID 1676488.
- Hooton, Earnest A. (22 January 1926). "Methods of Racial Analysis". Science. 63 (1621): 75–81. Bibcode:1926Sci....63...75H. doi:10.1126/science.63.1621.75. PMID 17774966.
- James, Michael (28 May 2008). "Race". In Zalta, Edward N. (ed.). The Stanford Encyclopedia of Philosophy (Spring 2017 ed.). Metaphysics Research Lab, Stanford University.
- Jorde, L. B.; Wooding, S. P. (November 2004). "Genetic variation, classification and 'race'". Nature Genetics. 36 (11 Suppl): S28 – S33. doi:10.1038/ng1435. PMID 15508000.
- Joseph, Celucien L. (2012). Race, Religion, and The Haitian Revolution: Essays on Faith, Freedom, and Decolonization. CreateSpace Independent Publishing Platform.
- Joseph, Celucien L. (2013). From Toussaint to Price-Mars: Rhetoric, Race, and Religion in Haitian Thought. CreateSpace Independent Publishing Platform.
- Keita, S. O. Y.; Kittles, R. A. (1997). "The persistence of racial thinking and the myth of racial divergence". American Anthropologist. 99 (3): 534–544. doi:10.1525/aa.1997.99.3.534.
- Krimsky, Sheldon; Sloan, Kathleen, eds. (2011). Race and the Genetic Revolution: Science, Myth, and Culture. Columbia University Press. ISBN 978-0-231-52769-9.
- Mayr, Ernst (1969). Principles of Systematic Zoology. New York: McGraw-Hill. ISBN 0-07-041143-3.
- Mayr, Ernst (Winter 2002). "The Biology of Race and the Concept of Equality". Daedalus. 31 (1). MIT Press on behalf of American Academy of Arts & Sciences: 89–94. JSTOR 20027740.
- Patten, M. A.; Unitt, P. (2002). "Diagnosability versus mean differences of sage sparrow subspecies". Auk. 119 (1): 26–35. doi:10.1642/0004-8038(2002)119[0026:DVMDOS]2.0.CO;2. S2CID 86356616.
- Shriver, M. D.; Kittles, R. A. (2004). "Opinion: Genetic ancestry and the search for personalized genetic histories". Nature Reviews Genetics. 5 (8): 611–618. doi:10.1038/nrg1405. PMID 15266343. S2CID 4465469.
- Smedley, A.; Smedley, B. D. (January 2005). "Race as biology is fiction, racism as a social problem is real: Anthropological and historical perspectives on the social construction of race" (PDF). American Psychologist. 60 (1): 16–26. doi:10.1037/0003-066X.60.1.16. PMID 15641918.
- Stanton, W. (1982) [1960]. The leopard's spots: scientific attitudes toward race in America, 1815–1859. University of Chicago Press. ISBN 0-226-77122-9.
- Sussman, Richard Wald (2014). The Myth of Race: The Troubling Persistence of an Unscientific Idea. Harvard University Press. ISBN 978-0-674-41731-1.
- Tishkoff, Sarah A.; Kidd, Kenneth K. (2004). "Implications of biogeography of human populations for 'race' and medicine". Nature Genetics. 36 (11 Suppl): S21 – S27. doi:10.1038/ng1438. PMID 15507999.
- Travassos, Claudia; Williams, David R. (June 2004). "The concept and measurement of race and their relationship to public health: a review focused on Brazil and the United States" (PDF). Cadernos de Saúde Pública. 20 (3): 660–678. doi:10.1590/S0102-311X2004000300003. PMID 15263977.
- "UNESCO and Its Programme: The Race Question" (PDF). Paris: UNESCO. 1950. Publication 791.
- "The Race Concept: Results of an Inquiry". Paris: UNESCO. 1952. Document code: SS.53/II.9/A.
- "Four Statements on the Race Questions". Paris: UNESCO. 1969. Document code: COM.69/II.27/A.
- von Vacano, Diego (2011). The Color of Citizenship: Race, Modernity and Latin American/Hispanic Political Thought. Oxford University Press.
- Wade, Peter (2002). Race, Nature and Culture: An anthropological perspective. London: Pluto Press. ISBN 0-7453-1459-7.
- Waples, Robin S.; Gaggiotti, Oscar (2006). "What is a population? An empirical evaluation of some genetic methods for identifying the number of gene pools and their degree of connectivity". Molecular Ecology. 15 (6): 1419–1439. doi:10.1111/j.1365-294X.2006.02890.x. PMID 16629801. S2CID 9715923.
- Whitmarsh, Ian; Jones, David S., eds. (2010). What's the Use of Race?: Modern Governance and the Biology of Difference. Cambridge, Massachusetts: MIT Press. ISBN 978-0-262-51424-8. Lay summary Archived 2 February 2022 at the Wayback Machine (28 April 2013) This review of current research includes chapters by Ian Whitmarsh, David S. Jones, Jonathan Kahn, Pamela Sankar, Steven Epstein, Simon M. Outram, George T. H. Ellison, Richard Tutton, Andrew Smart, Richard Ashcroft, Paul Martin, George T. H. Ellison, Amy Hinterberger, Joan H. Fujimura, Ramya Rajagopalan, Pilar N. Ossorio, Kjell A. Doksum, Jay S. Kaufman, Richard S. Cooper, Angela C. Jenks, Nancy Krieger, and Dorothy Roberts.
- Wilson, J. F.; Weale, M. E.; Smith, A. C.; Gratrix, F.; Fletcher, B.; Thomas, M. G.; Bradman, N.; Goldstein, D. B. (2001). "Population genetic structure of variable drug response". Nature Genetics. 29 (3): 265–269. doi:10.1038/ng761. PMID 11685208. S2CID 25627134.
Popular press
[edit]- Dawkins, Richard (23 October 2004). "Race and creation". Prospect. Extract from Dawkins, Richard (17 December 2023). The Ancestor's Tale: A Pilgrimage to the Dawn of Evolution. Houghton Mifflin Harcourt. ISBN 978-0-61-861916-0.
- Krulwich, Robert (2 February 2009). "Your Family May Once Have Been a Different Color". Morning Edition. National Public Radio.
- Leroi, Armand Marie (14 March 2005). "A Family Tree in Every Gene". The New York Times.
- "The Nature of Normal Human Variety: A Talk with Armand Marie Leroi". Edge Foundation. 13 March 2005.
- "The Myth of Race". Medicine Magazine. 2007. Archived from the original on 1 January 2009.
External links
[edit]- Hopper, Allison (5 July 2021). "Race, Evolution and the Science of Human Origins". Scientific American.
- "When racism was respectable: Franz Boas on The Categorization of Human Types". History Matters. George Mason University.
- "Race". Stanford Encyclopedia. Stanford University. 17 December 2023.
- Geoffrey Galt Harpham (ed.). "Theories of race. An annotated anthology of essays on race, 1684–1900".
- "Race – The Power of an Illusion". PBS.org. Public Broadcasting Service. 2003. Archived from the original on 23 April 2003. Companion website to California Newsreel feature.
- "Is Race 'Real'?". RaceAndGenomics.SSRC.org. Social Science Research Council. Archived from the original on 17 November 2017. Retrieved 25 April 2005. A collection of essays by professors and research scientists.
Official statements
[edit]- "Statement on Race & Racism". PhysAnth.org. American Association of Physical Anthropologists. 2019.
- "Race". State & County QuickFacts. US Census Bureau. 2000. "Definition" section. Archived from the original on 9 May 2008.
- "Standards for Maintaining, Collecting, and Presenting Federal Data on Race and Ethnicity". DoI.gov. US Department of Interior. 1997. Archived from the original on 4 October 2003. Originally published in Federal Register, 30 October 1997.
- "Race: Are We So Different? (Understanding Race)". American Anthropological Association. 2007–2020. Archived from the original on 1 September 2019. A public education program, including history, human variation, and lived experience.
Race (human categorization)
View on GrokipediaBiological Foundations
Genetic Evidence for Population Clusters
Analyses of human genetic variation using model-based clustering methods, such as the STRUCTURE software, have consistently identified discrete population clusters that align with continental-scale geographic ancestries. In a seminal 2002 study, Rosenberg et al. genotyped 377 autosomal microsatellite loci across 1,056 individuals from 52 populations worldwide, revealing that when assuming five to six inferred clusters (K=5–6), the groupings corresponded closely to major regions: sub-Saharan Africa, Europe plus the Middle East, Central and South Asia, East Asia, Oceania, and the Americas.[1][2] These clusters emerged despite gene flow, as allele frequencies showed geographic continuity, with admixture zones (e.g., Central Asia) exhibiting intermediate assignments.[8] Principal component analysis (PCA) of genome-wide data further corroborates these clusters by projecting genetic variation onto low-dimensional axes that separate populations by ancestry. For instance, the first principal component (PC1) typically distinguishes sub-Saharan Africans from non-Africans due to the out-of-Africa bottleneck, while PC2 differentiates East Asians from Europeans and South Asians.[9] Studies using thousands of single nucleotide polymorphisms (SNPs) or whole-genome sequences, such as those from the Human Genome Diversity Project, produce PCA plots where individuals cluster tightly by self-reported or sampled continental origin, with clinal variation within but sharp boundaries between clusters.[10] This structure persists even after accounting for linkage disequilibrium, enabling ancestry inference with over 99% accuracy for major groups in forensic and medical applications.[11] The fixation index (FST), a measure of genetic differentiation, quantifies between-population variance as approximately 10–15% for continental-scale comparisons, indicating moderate but significant divergence driven by isolation, drift, and selection.[12] Pairwise FST values, for example, range from 0.12 between Europeans and East Asians to 0.19 between Africans and Oceanians, reflecting cumulative effects of serial founder events and local adaptation.[13] These values exceed those seen in many species considered subspecies (e.g., chimpanzees, FST ≈ 0.18–0.25), underscoring that human populations exhibit structured differentiation amenable to clustering.[14] A common counterargument, originating from Lewontin's 1972 analysis of 17 blood protein loci, posits that 85% of human genetic variation occurs within populations versus 15% between them, suggesting races lack biological reality.[15] However, A.W.F. Edwards demonstrated in 2003 that this apportionment—focusing on single-locus variance—overlooks multivariate correlations across loci, which enable reliable cluster detection akin to distinguishing iris species via calyx measurements despite overlapping traits.[16][17] Empirical reanalyses confirm that while within-group variance dominates at individual loci, the covariance structure across the genome yields discrete clusters predictive of ancestry, refuting claims that high intrapopulation diversity negates interpopulation structure.[18] Recent whole-genome sequencing of diverse cohorts, including over 900 individuals from 54 populations, reinforces these findings with finer-resolution clusters incorporating structural variants and rare alleles, which amplify differentiation signals.[19] Such evidence supports population clusters as empirical reflections of historical demography, with implications for disease risk alleles (e.g., higher frequencies of certain variants in specific clusters) and pharmacogenomics.[20] Despite admixture in modern populations, core clusters remain robust, as validated by supervised learning algorithms assigning admixed individuals to ancestral proportions with high fidelity.[21]Phenotypic and Physiological Variations
Human populations display phenotypic variations in traits such as skin pigmentation, hair texture, eye shape, and body proportions that align with genetic clusters corresponding to continental ancestries. These differences arose from natural selection pressures, including ultraviolet radiation levels, climate, and diet, leading to adaptive divergences over millennia. For instance, skin color gradients reflect melanin production optimized for UV protection in high-sunlight equatorial regions and vitamin D synthesis in low-sunlight higher latitudes, with darker pigmentation predominant in sub-Saharan African populations and lighter tones in European and East Asian groups.[22] Genetic variants, such as those in the SLC24A5 and MC1R genes, account for much of this variation, with the derived allele for lighter skin fixed in Europeans around 10,000 years ago.[23] Hair morphology also varies systematically: tightly coiled hair is characteristic of African-descended populations, aiding thermoregulation through scalp insulation; straight, thick hair predominates in East Asians due to EDAR gene variants enhancing hair shaft growth; and wavy or curly forms are common in Europeans and South Asians.[24] Craniofacial features, including nasal breadth (wider in tropical populations for humid air warming) and epicanthic folds (prevalent in East Asians for cold/dry wind protection), follow similar geographic patterns per Allen's and Thomson's rules.[25] Average stature and limb proportions differ as well, with longer limbs relative to torso in equatorial groups per Allen's rule for heat dissipation, and stockier builds in Arctic populations like Inuit for heat conservation under Bergmann's rule; global data show sub-Saharan Africans averaging shorter heights (e.g., 169 cm for men in some groups) compared to Northern Europeans (178 cm).[26] Physiological variations include metabolic adaptations, such as adult lactose persistence, enabled by a mutation in the LCT gene upstream promoter, reaching frequencies of 80-95% in Northern European and pastoral African populations but near 0% in East Asians and Native Americans, reflecting dairy domestication histories post-7,000 BCE.[27] The sickle cell trait (HbS allele) provides malaria resistance in heterozygotes, with carrier rates up to 20-30% in West African and Indian populations from malaria-endemic zones, but rare elsewhere, demonstrating local selective pressures.[28] High-altitude adaptations, like the EPAS1 gene variant in Tibetans enabling efficient hypoxia response without excessive red blood cell production, evolved within the last 3,000 years, distinct from Andean or Ethiopian variants.[29] Athletic performance disparities show genetic underpinnings, with West African-descended individuals dominating elite sprinting due to higher frequencies of fast-twitch muscle fiber variants (e.g., ACTN3 R allele) and lower body fat, explaining near-monopoly in events under 400m since 1968 Olympic data.[30] Conversely, East African Rift Valley populations excel in distance running, linked to enhanced running economy, mitochondrial efficiency, and slender morphology from genes like ACE and mitochondrial DNA haplogroups.[31] Blood group distributions vary, with type B higher in Central Asians (up to 30%) versus lower in Europeans (10-15%), serving as neutral markers of population history.[25] These traits exhibit concordance within clusters despite clinal elements, underscoring evolutionary divergence rather than uniform human homogeneity.[32]Evolutionary Origins and Admixture
Modern humans (Homo sapiens) originated in Africa approximately 300,000 years ago, with genetic evidence indicating initial population structure within the continent that predated major out-of-Africa migrations.[33] Subsequent dispersals, beginning around 70,000–60,000 years ago, led to the peopling of Eurasia and beyond, where geographic isolation fostered genetic divergence through drift and local selection pressures.[34] These processes resulted in distinct population clusters corresponding to continental-scale groups, with pairwise FST values around 0.15 indicating moderate differentiation driven by serial founder effects and adaptation to varied environments.[35] Divergence timelines from genetic distance estimates place the initial split between African and non-African lineages at roughly 120,000 years ago, followed by further branching, such as between East Asians and Europeans around 40,000–30,000 years ago.[35] Selection acted on standing variation and new mutations to produce regionally specific traits; for instance, lighter skin pigmentation evolved in northern latitudes via alleles in genes like SLC24A5 and SLC45A2, enhancing vitamin D synthesis under low UV exposure, with key variants arising over 500,000 years ago but fixing post-migration.[36] Similarly, lactase persistence (LCT gene) spread rapidly in Eurasian pastoralist groups after ~10,000 years ago, conferring caloric advantages in dairy-reliant diets, while sickle-cell trait (HBB gene) maintained heterozygote advantage in malaria-endemic African regions.[37] These adaptations reflect causal responses to climate, pathogens, and subsistence shifts rather than neutral drift alone.[38] Admixture events punctuated this divergence, introducing archaic DNA into modern lineages. Non-African populations carry 1–2% Neanderthal ancestry from interbreeding ~50,000–60,000 years ago in Eurasia, with East Asians showing slightly higher proportions; Denisovan admixture, up to 4–6% in Melanesians and lower in East Asians, occurred separately in Asia.[39] [40] Later pulses, including back-migrations into Africa ~3,000 years ago, added non-local Eurasian alleles to some sub-Saharan groups, though African genomes retain the highest overall diversity due to longer effective population sizes.30175-2) Such gene flow blurred boundaries but preserved core cluster structures, as evidenced by principal component analyses of genome-wide SNPs aligning with geographic origins.[41]Historical Classifications
Pre-Modern and Early Modern Observations
Ancient Greek writers, such as Herodotus in the 5th century BCE, documented physical variations among peoples encountered during travels, describing Egyptians as having "skin burnt by the sun" and "woolly hair," akin to their southern neighbors, while distinguishing eastern Ethiopians by straight hair contrasting with the curly-haired variety.[42][43] Herodotus also noted the Colchians' dark skin and woolly hair as evidence of Egyptian origins, linking such traits to shared customs rather than solely environmental factors.[44] Greek and Roman authors generally attributed skin tone differences—paler northerners, olive Mediterraneans, and darker southerners—to climate, as in the Hippocratic Airs, Waters, Places (c. 400 BCE), which posited that hot, dry environments produced darker, more robust physiques with curly hair, while colder zones yielded lighter skin and straighter hair.[45][46] Roman observers extended these environmental theories, with writers like Vitruvius (1st century BCE) claiming northern peoples had ruddy complexions and vigorous builds due to cold air, contrasting with the slender, darker southerners shaped by heat.[46] Physical distinctions were acknowledged in art and literature—Ethiopians depicted with dark skin in mosaics and texts—but categorization emphasized cultural practices, language, and loyalty to Rome over immutable biological lines, without systematic racial hierarchies based on color alone.[47][48] In medieval Islamic scholarship, Ibn Khaldun's Muqaddimah (1377 CE) analyzed human variations across climatic zones, arguing that temperate regions fostered balanced physiques and intellects, while extremes produced either overly robust, dark-skinned desert nomads or pallid, sedentary urbanites; he viewed these as adaptive responses to environment rather than fixed racial essences, rejecting inherent superiority while noting observable traits like skin tone and hair texture.[49][50] Pre-modern Christian interpretations drew from Genesis 10's Table of Nations, tracing post-flood humanity to Noah's sons—Japheth to Europeans, Ham to Africans and Canaanites, Shem to Semites—implying descent-based divisions later mapped onto physical differences, though early exegeses focused more on geography and lineage than phenotype.[51][52] Early modern European explorers amplified these observations through direct encounters. Christopher Columbus, in his 1492 journal, described Caribbean natives as "well-formed" with "hair black and straight," skin tones ranging from tawny to reddish-brown, distinct from Europeans yet akin to some Asians in feature.[53] Ferdinand Magellan's circumnavigation (1519–1522) accounts noted Philippine islanders' brown skin, straight black hair, and tattooed bodies, categorizing them as separate from both Old World Africans and Amerindians based on morphology and customs.[54] These reports, disseminated via letters and chronicles, highlighted heritable physical clusters—e.g., Amerindians' epicanthic folds and broad faces—prompting initial categorizations by continent of origin rather than climate alone, though environmental adaptation remained a common explanation.[55]18th-19th Century Taxonomic Systems
In 1735, Swedish naturalist Carl Linnaeus published the first edition of Systema Naturae, introducing a taxonomic classification of humans as a single species, Homo sapiens, divided into four continental varieties based on geography, skin color, temperament, and physical traits: the European (europaeus albus, white, sanguine, and inventive), American (americanus rubescens, red, choleric, and stubborn), Asiatic (asiaticus fuscus, yellow, melancholic, and greedy), and African (afer niger, black, phlegmatic, and lazy).[56][57] Linnaeus's system emphasized observable phenotypic differences and assigned behavioral stereotypes derived from travel accounts and classical sources, positioning humans within the broader animal kingdom as primates.[58] By the 10th edition in 1758, these were formalized as subspecies, influencing subsequent European natural history by providing a binomial nomenclature framework applied to human variation.[59] German physician Johann Friedrich Blumenbach expanded this approach in his 1775 dissertation De Generis Humani Varietate Nativa (On the Natural Varieties of Mankind), classifying humans into five races derived from craniometric analysis of 63 skulls: Caucasian (white-skinned, from the Caucasus region, deemed the primordial form due to skull beauty), Mongolian (yellow-skinned East Asians), Ethiopian (black-skinned Africans), American (red-skinned Native Americans), and Malayan (brown-skinned Southeast Asians and Pacific Islanders).[60][59] Blumenbach, a monogenist, argued these varieties arose from environmental degeneration from a Caucasian archetype rather than separate creations, using metrics like facial angle and skin pigmentation while rejecting temperament-based stereotypes.[61] His 1795 third edition reinforced skin color as a key marker and popularized "Caucasian" as a term for Europeans, shaping physical anthropology by prioritizing skeletal evidence over Linnaean psychology.[62] French naturalist Georges Cuvier, in early 19th-century works like Le Règne Animal (1817), proposed a tripartite division into Caucasian (white), Mongolian (yellow), and Ethiopian (black) races, viewing them as persistent branches of a common stock with fixed physiological differences in stature, cranial structure, and intellect, where Caucasians represented the highest development.[63][64] Cuvier's functionalist anatomy emphasized adaptive traits tied to climate and lifestyle, influencing catastrophist geology and polygenist debates by implying greater permanence in racial distinctions than Blumenbach allowed.[65] These systems collectively advanced empirical taxonomy through metrics like skin hue, hair texture, and osteology, though reliant on limited specimens and Eurocentric collections, laying groundwork for 19th-century anthropometry despite monogenist-polygenist tensions.[59]Polygenism, Monogenism, and Eugenics Debates
Monogenism, the view that all human races descended from a single ancestral pair, dominated early modern racial classifications and aligned with biblical accounts of a common human origin. Johann Friedrich Blumenbach, in his 1775 work De Generis Humani Varietate Nativa, classified humans into five varieties—Caucasian, Mongolian, Ethiopian, Malayan, and American—while maintaining monogenism through a degenerative hypothesis, positing that environmental factors caused deviations from an original Caucasian prototype without separate creations.[66] This framework emphasized species unity, though it implied a hierarchy with Europeans as least degenerated. Monogenists like Blumenbach rejected polygenism partly on empirical grounds, citing inter-racial fertility and anatomical similarities as evidence against distinct origins.[59] Polygenism emerged as a counter-theory in the early 19th century, asserting separate creations or origins for major racial groups, often to rationalize observed physical and intellectual differences as innate and immutable. American physician Samuel George Morton advanced polygenism through craniometric studies; in Crania Americana (1839), he reported average cranial capacities of 87 cubic inches for Caucasians, 82 for Native Americans, and 78 for Africans, interpreting these as fixed racial traits incompatible with monogenist degeneration from a single stock.[67] Swiss naturalist Louis Agassiz, upon immigrating to the United States in 1846 and joining Harvard, publicly endorsed polygenism in lectures and writings, arguing that geographical isolation produced distinct human "species" akin to animal varieties, with Blacks exhibiting subhuman traits like laziness and low intellect.[68] Proponents like Morton and Agassiz, alongside Josiah Nott and George Gliddon in Types of Mankind (1854), used such data to challenge abolitionism, claiming racial hierarchies were divinely ordained rather than environmentally induced.[69] Recent reanalyses confirm Morton's measurements were accurate within 19th-century methods, undermining claims of deliberate bias in his rankings.[70] These origin debates intersected with eugenics, a movement formalized by Francis Galton in 1883, which sought to enhance human qualities through selective breeding based on presumed hereditary racial and class differences. Galton, drawing from his 1869 observations of African cognitive capacities during travels, concluded in Hereditary Genius (1869) that intellectual traits were biologically fixed and unevenly distributed across races, with Europeans superior; he advocated "positive eugenics" to encourage reproduction among the talented and restrict it among inferiors, implicitly extending polygenist assumptions of unbridgeable gaps.[71] While Galton leaned monogenist in rejecting separate creations, eugenics amplified polygenist implications by treating racial traits as stable inheritance units, influencing policies like U.S. immigration quotas (1924) and sterilizations (over 60,000 by 1930s) targeting "dysgenic" groups including non-Europeans.[72] Critics within science, including Darwin, opposed polygenism's denial of common descent, but eugenicists repurposed cranial and anthropometric data to argue for interventionist realism over egalitarian monogenism.[73] The debates waned post-Darwin with genetic evidence favoring recent common ancestry, yet they shaped persistent views on racial causality in heredity.[74]Social and Cultural Dimensions
Race as Folk Taxonomy in Different Societies
In many societies, folk taxonomies of race emerge as intuitive, non-scientific systems for grouping humans based on observable phenotypic traits such as skin color, facial features, and hair texture, often reflecting local histories of migration, admixture, and social interaction rather than global biological clusters.[75] These classifications prioritize practical social utility over precision, varying significantly across cultures; for instance, while some emphasize discrete categories, others employ continua or emphasize ancestry and status alongside appearance.[76] Empirical studies of everyday cognition show that such folk systems can capture coarse-grained patterns of human variation that partially align with genetic ancestry, though they are shaped by cultural lenses and do not equate to rigorous taxonomy.[77] In the United States, folk racial categorization historically follows a hypodescent rule for African ancestry, classifying individuals with any detectable sub-Saharan heritage as Black, alongside broad groups like White (European descent), Asian (East/South Asian), Hispanic (often treated as ethnic overlay), and Native American.[78] This binary-tending system, rooted in colonial-era one-drop rules, contrasts with more fluid Latin American approaches; U.S. Census data from 2020 reported 57.8 million identifying as Hispanic/Latino (any race), 41.1 million as Black alone, and 33.9 million as Asian alone, illustrating how self-identification intersects with imposed folk norms. In Brazil, by comparison, the 2022 census categorized 43.1% as Pardo (mixed European-African-Indigenous), 45.3% as White, 10.2% as Black, and 0.4% as Indigenous, reflecting a phenotype-driven spectrum where terms like moreno (brown) or caboclo (Indigenous-mixed) denote gradients rather than fixed bins, influenced by socioeconomic mobility and "whitening" aspirations. This fluidity, documented in surveys where the same individual might receive different classifications based on context or interviewer perception, underscores how status and appearance modulate folk assignments in mestizo-heavy societies.[76][79] Sub-Saharan African folk taxonomies prioritize ethnic and linguistic affiliations over continental racial unity, with over 2,000 groups like the Yoruba, Zulu, or Maasai viewing each other as distinct based on language, customs, and territorial rivalry, often subsuming skin color variation under tribal identity.[80] Encounters with Europeans historically prompted terms like "white people" (e.g., abule in Yoruba for outsiders) or Arabs/North Africans as separate, but internal diversity—such as lighter-skinned East Africans (e.g., Nilotes) versus darker West Africans—leads to subgroupings by stature, scarification, or ecology rather than a monolithic "Black" category.[81] In India, folk perceptions blend racial elements with caste endogamy, where fairer northern Indo-Aryan phenotypes contrast with darker southern Dravidian ones, yielding informal hierarchies like "high-caste fair" versus "tribal dark," though anthropological surveys identify folk clusters akin to Negrito, Proto-Australoid, and Mongoloid in northeastern hill tribes.[82] Colorism manifests in marriage preferences, with 2019 studies showing 70-80% of matrimonial ads specifying "fair complexion," reflecting a folk taxonomy where skin tone signals ancestral purity or status beyond formal varna.[83] East Asian societies, particularly China, employ folk taxonomies centered on the Han majority (91.1% of 1.41 billion population in 2020) distinguishing minorities like Uyghurs or Tibetans by phenotype and culture, while globally framing outsiders as "white" (Europeans), "black" (Africans), or "yellow" kin (other East Asians). This yields a tripartite worldview—yellow self, white advanced but alien, black primitive—evident in historical texts and modern attitudes, where surveys indicate 60-70% of urban Chinese associate Africans with lower socioeconomic traits based on visible differences.[84] Such categorizations, less rigid than Western binaries, integrate ethnicity (minzu) with racial cues, as seen in policies recognizing 55 minorities since 1954, yet folk usage often defaults to phenotypic shorthand amid limited admixture.[85] Across these examples, folk taxonomies demonstrate adaptability to local demographics, with empirical consistency in recognizing major migratory divides (e.g., African, European, Asian clusters) despite cultural variances.[86]Influence of Colonialism and Nationalism
Colonial expansion from the 15th to 19th centuries prompted European powers to develop racial classifications as tools for administering diverse conquered populations and justifying exploitation. In the Americas, initial distinctions based on religion and status shifted toward hereditary racial categories by the late 17th century, with colonial legislatures enacting laws that defined blackness as a permanent, inheritable condition tied to enslavement.[87] [88] For instance, Virginia's 1662 statute decreed that children of enslaved African women inherited their mother's status regardless of the father's race, embedding racial hierarchy into legal frameworks to sustain labor systems.[88] Similar mechanisms emerged in other colonies, where racial typologies facilitated the commodification and control of indigenous and African peoples, transforming fluid ethnic identities into rigid, descent-based groups.[89] [90] These colonial practices entrenched racial categories by prioritizing phenotypic markers like skin color and ancestry for governance and resource extraction, often overriding pre-existing social structures. In British and Dutch colonies in Africa and Asia, administrators imposed segregated classifications that ranked Europeans above locals, using pseudoscientific metrics to allocate rights and labor roles.[89] This approach not only rationalized slavery—evident in the transatlantic trade's peak of over 12 million Africans forcibly transported between 1500 and 1866—but also laid groundwork for post-colonial ethnic divisions by institutionalizing race as a proxy for loyalty and capacity.[55] [91] Critics of conventional narratives argue that such categorizations arose reactively from the logistical demands of empire rather than pre-existing animus, with economic imperatives driving the solidification of racial binaries like "white" versus "non-white."[55] Nationalism in the 19th century further fused racial identity with state-building, portraying nations as extensions of biologically distinct peoples to mobilize populations for unification and expansion. In Europe, Romantic-era thinkers linked linguistic and cultural unity to racial purity, as seen in German nationalists' emphasis on Teutonic descent from the 1810s onward, which influenced policies excluding "alien" groups.[92] In the United States, post-independence nationalism codified racial categories in the 1787 Constitution's three-fifths clause and subsequent laws, framing white Anglo-Saxon identity as foundational to republican virtue amid territorial growth.[93] This ethnic-nationalist paradigm, peaking during the 1848 revolutions and imperial scrambles, justified conquests—such as the U.S. acquisition of over 500,000 square miles via the 1848 Mexican-American War—by invoking racial superiority over "inferior" populations.[92] Such nationalist ideologies amplified colonial legacies by essentializing race as a determinant of national character, evident in exclusionary citizenship laws like the U.S. Naturalization Act of 1790, which limited eligibility to "free white persons."[93] In settler societies, this reinforced hierarchies, with over 90% of U.S. land west of the Mississippi claimed under doctrines tying Manifest Destiny to racial providence by 1890.[92] While these frameworks drew on observed continental ancestries, they selectively ignored admixture to serve political ends, contributing to enduring categorizations that conflate folk biology with civic belonging.[94] Empirical analyses note that nationalism's racialization intensified disparities, as in Europe's post-1871 German Empire, where policies favored "Aryan" elements amid industrialization.[95]Modern Variations in Racial Categorization
In the United States, federal standards for racial and ethnic data collection, established by the Office of Management and Budget (OMB), were revised in March 2024 to include seven minimum categories: American Indian or Alaska Native, Asian, Black or African American, Hispanic or Latino, Middle Eastern or North African, Native Hawaiian or Pacific Islander, and White.[96] These updates, building on the 1997 framework, combine race and ethnicity into co-equal categories, permit multiple selections to reflect multiracial identities, and emphasize self-identification while allowing observer classification in certain contexts like law enforcement.[97] The 2020 Census reported 33.8 million people selecting two or more races, up from 9 million in 2010, highlighting increasing acknowledgment of admixture.[98] In Brazil, racial categorization relies primarily on self-perception influenced by skin color and appearance, with the 2022 Census using five categories: White (branco, 43.5%), Brown (pardo, 45.3%), Black (preto, 10.2%), Indigenous (0.8%), and Asian (0.4%).[99] This system contrasts with binary models by accommodating a continuum of mixtures, where pardo encompasses diverse African, European, and Native American ancestries; genetic studies confirm that self-identified pardos average 40-60% European, 20-40% African, and 10-20% Native American ancestry.[100] Recent trends show shifts in self-identification tied to skin tone, with darker individuals increasingly selecting Black over Brown amid affirmative action policies introduced in the 2000s.[101] European nations often eschew explicit racial categories in official data, favoring nationality, citizenship, or migration background; for instance, France prohibits census questions on race or ethnicity under republican principles, relying instead on birthplace proxies, while the United Kingdom's 2021 Census includes optional self-reported options like White, Asian/Asian British, Black/African/Caribbean/Black British, Mixed, and Other.[102] In South Africa, post-1994 classifications retain apartheid-era terms—Black African, White, Coloured, and Indian/Asian—for equity monitoring, with self-identification predominant but phenotypic assessments used historically.[103] Genetic approaches to categorization employ ancestry informative markers (AIMs) to infer continental origins, yielding clusters that align broadly with traditional races: sub-Saharan African, European, East Asian, Oceanian, and Native American, as demonstrated in STRUCTURE analyses with K=5 populations explaining 93-95% of variation.[104] Commercial tests like those from 23andMe report percentages from reference panels of over 100 global populations, revealing fine-scale structure (e.g., distinguishing Northern vs. Southern Europeans) but also admixture blurring boundaries; self-reported race correlates with these clusters at 99% accuracy for major groups in U.S. samples.[105] In medicine, race serves as a proxy for genetic ancestry in pharmacogenomics, such as adjusting warfarin dosing by African vs. European ancestry due to VKORC1 and CYP2C9 variants differing by 20-30% across clusters.[104] These methods underscore persistent biological discontinuities despite social fluidity.Perspectives from Scientific Disciplines
Anthropology and Physical Anthropology
Physical anthropology, a subfield of anthropology focused on the biological and behavioral aspects of humanity, has historically employed metrics such as craniometry, osteometry, and somatometry to assess human variation and classify populations into racial categories based on observable physical differences.[106] These methods measure traits including cranial capacity, facial prognathism, nasal index, and cephalic index, which exhibit average differences across continental populations; for instance, sub-Saharan African skulls tend to show greater prognathism and wider nasal apertures compared to European or East Asian skulls.[107] [108] Studies of cranial morphology reveal patterned variations that align with geographic ancestry, enabling forensic anthropologists to estimate ancestry with accuracies ranging from 80% to over 90% in controlled and casework settings, respectively.[109] [110] Such estimations rely on multivariate analyses of skeletal features, including the shape of the nasal aperture, zygomatic breadth, and mastoid process, which form distinct clusters corresponding to traditional racial groups like Caucasoid, Negroid, and Mongoloid.[111] These findings indicate that human physical variation includes discontinuities sufficient for practical categorization, despite clinal gradients in some traits like skin pigmentation.[112] While organizations such as the American Association of Biological Anthropologists have issued statements asserting that biological races do not exist—often emphasizing continuous variation and social construction over empirical clustering—physical anthropological data from global samples contradict blanket denials by demonstrating heritable, population-specific morphologies that persist even after accounting for environmental factors.[113] For example, analyses of 148 ethnic groups using geometric morphometrics confirm regional cranial form diversity that maps onto broad ancestral lineages, supporting the utility of race as a proxy for ancestry in contexts like bioarchaeology and identification.[112] This empirical approach prioritizes measurable traits over ideological assertions, highlighting how systemic biases in academic institutions may undervalue such evidence in favor of egalitarian premises lacking causal support from the data.[4]Genetics and Evolutionary Biology
Human genetic variation displays structured patterns that align with geographic and ancestral populations, enabling clustering of individuals into groups corresponding to traditional racial categories such as African, European, East Asian, and Native American ancestries. Analyses of genome-wide markers, including microsatellites and single nucleotide polymorphisms (SNPs), consistently reveal these clusters through methods like principal component analysis (PCA) and STRUCTURE algorithms, where individuals from the same continental region group together with high accuracy, even without prior geographic labels.[1] [18] This structure arises from historical isolation, migration bottlenecks, and differential gene flow, with non-African populations showing reduced heterozygosity due to serial founder effects during out-of-Africa dispersals estimated at 60,000–70,000 years ago.[114] [115] A common argument against the biological reality of such clusters stems from Lewontin's 1972 analysis, which apportioned 85% of variation to within-population differences and only 15% to between-group differences across loci. However, this overlooks the fact that small between-group differences, when correlated across thousands of loci, provide sufficient signal for reliable ancestry inference and classification, as demonstrated by multivariate statistical methods. A.W.F. Edwards critiqued this as a fallacy, noting that independent loci would yield overlapping distributions, but real genomes exhibit linkage disequilibrium and allele frequency covariation that delineate populations effectively, akin to how taxonomists distinguish subspecies despite comparable F_ST values.[2] [116] Empirical studies confirm this, with forensic and ancestry testing achieving over 99% accuracy in assigning individuals to continental origins using hundreds of markers.[117] The fixation index (F_ST), measuring population differentiation, averages 0.12 between continental groups, reflecting moderate divergence driven by genetic drift, selection, and limited admixture over millennia. This level exceeds that within many accepted animal subspecies and supports viewing human races as differentiated populations rather than arbitrary social constructs.[118] Evolutionary pressures post-dispersal have further accentuated differences: for instance, the SLC24A5 allele for lighter skin swept to near fixation in Europeans within the last 10,000 years for vitamin D synthesis in low-UV environments, while EPAS1 variants in Tibetans, derived from Denisovan admixture, enable hypoxia tolerance at high altitudes via modified hemoglobin response.[119] Other examples include lactase persistence mutations (LCT gene) independently evolving in European and East African pastoralists for adult milk digestion, and Duffy-null alleles conferring malaria resistance predominantly in West African-descended populations.[120] These adaptations, confirmed by haplotype scans and functional assays, underscore causal links between ancestry, environment, and genetic outcomes, with F_ST for adaptive loci often exceeding neutral averages.[121] Such patterns refute claims of human genetic uniformity by highlighting both neutral drift—evident in allele frequency clines across continents—and positive selection signatures, as in immune genes like HLA where population-specific alleles reflect pathogen pressures (e.g., higher diversity in Africans due to longer exposure histories). Genome projects like 1000 Genomes reveal that while total variation is clinal in some regions, discrete clusters predominate globally, with admixture zones (e.g., Latin America) as exceptions rather than the rule. This biological foundation informs evolutionary models of human diversification, where races represent adaptive radiations within a single species, without implying fixed hierarchies (i.e., inherent rankings of superiority or ability among races) but affirming empirically verifiable subgroup distinctions.[122]Medicine, Pharmacology, and Health Outcomes
Racial ancestries associated with traditional human racial categories exhibit distinct patterns in disease susceptibility due to genetic variants shaped by evolutionary pressures and population histories. For instance, sickle cell disease, caused by a mutation in the HBB gene providing partial malaria resistance, affects over 90% of diagnosed cases in the United States among individuals of non-Hispanic Black or African American descent, with carrier rates reaching 1 in 12 in this group compared to negligible prevalence in Europeans.[123] Similarly, hypertension prevalence among U.S. adults aged 18 and older stands at 58.0% for non-Hispanic Black individuals versus 44.5% overall, with genetic factors such as variants in salt-handling genes contributing to higher sodium sensitivity in populations of West African ancestry.[124] Diabetes rates also differ markedly, at 16% for Black adults and 18% for American Indian/Alaska Native adults compared to lower figures in other groups, linked in part to alleles like those in the TCF7L2 gene more frequent in certain ancestries.[125] In pharmacology, pharmacogenomic variants show substantial allele frequency differences across ancestries, enabling prediction of metabolic phenotypes with high accuracy and influencing drug efficacy and toxicity. The CYP2D6 enzyme, critical for metabolizing 20-25% of clinical drugs including antidepressants and opioids, displays reduced-function alleles comprising 35% of variation in African and African American populations versus lower rates in Europeans, leading to poorer activation of prodrugs like codeine into morphine.[126][127] African ancestry correlates with altered responses to therapies such as ACE inhibitors for hypertension, where genetic markers outperform self-reported race in predicting outcomes, underscoring ancestry's role over social constructs alone.[128] A landmark example is BiDil (hydralazine/isosorbide dinitrate), approved by the FDA in 2005 specifically for self-identified Black patients with heart failure after trials showed a 43% mortality reduction in this group, where the combination addresses nitric oxide pathway deficiencies more prevalent in West African-descended populations.[129] These patterns inform precision medicine, where ancestry-informed dosing guidelines mitigate adverse events; for example, higher warfarin dose requirements in individuals of African ancestry due to VKORC1 and CYP2C9 variants reduce bleeding risks.[126] Empirical data refute blanket denial of such differences, as genome-wide studies confirm continental-scale genetic clusters aligning with racial categories predict health risks better than ignoring them, despite critiques framing race-based approaches as marketing rather than biology.[130][126] Health outcomes reflect these realities: prostate cancer mortality is twofold higher in Black men, tied to androgen receptor variants, while East Asians show lower hepatocellular carcinoma rates absent in Europeans due to selection against HBV-susceptible alleles.[131] Integrating ancestry data thus enhances diagnostic accuracy and treatment, as evidenced by FDA pharmacogenomic labeling incorporating racial/ethnic frequencies for over 200 drugs.[126]Key Controversies and Empirical Debates
Critiques of Race Denialism and Lewontin's Fallacy
Race denialism posits that human racial categories lack a substantive biological basis, emphasizing instead that genetic differences between purported racial groups are negligible compared to those within groups. This view frequently invokes Richard Lewontin's 1972 analysis of 17 polymorphic loci across human populations, which apportioned genetic variation as approximately 85% within local populations, 8% between populations within races, and 7% between races.[132] Proponents argue this distribution undermines the validity of race as a taxonomic unit, suggesting human genetic diversity defies discrete grouping.[133] A central critique labels this reasoning Lewontin's fallacy, as articulated by geneticist A.W.F. Edwards in 2003. Edwards contended that Lewontin's single-locus variance apportionment overlooks the multivariate structure of genetic data: while individual loci show high within-group variation, correlations across multiple loci enable reliable clustering of individuals into ancestral populations. For instance, even modest allele frequency differences (e.g., 5-10%) at numerous loci compound to produce distinct probabilistic profiles, akin to how subtle morphological variances distinguish species in classical taxonomy despite overlapping traits.[134] Edwards demonstrated this using Fisher's discriminant analysis on Lewontin's data, showing populations separable with error rates below 1%, illustrating that between-group signals persist amid within-group noise.[16] Population genetic studies reinforce this by revealing hierarchical clustering. Rosenberg et al. (2002) applied the STRUCTURE algorithm to 1,056 individuals across 52 populations with 377 microsatellite loci, identifying five major clusters aligning with continental ancestry (Africa, Europe/Middle East, East Asia, Melanesia, Americas) at K=5, with 99% of individuals assigning to their continental group at K=6. Subsequent analyses with denser SNP data (e.g., over 600,000 markers) confirm these clusters, where average pairwise genetic distances (F_ST) between continental groups range from 0.12 to 0.15, reflecting cumulative divergence from serial founder effects and local adaptation over 50,000-100,000 years. Such clustering validates race as coarse-grained proxies for ancestry, contradicting denialist claims of arbitrariness. Critics of denialism argue it misapplies Lewontin's metric by ignoring higher-order correlations and practical discriminability, often prioritizing egalitarian priors over empirical patterns. Geneticist David Reich has noted that denying population-specific variants—evident in traits like lactase persistence (prevalent in 70-90% of Northern Europeans vs. <10% in East Asians)—stifles inquiry into causal mechanisms, as STRUCTURE-like methods consistently recover geographic-genetic continuity.[135] This fallacy persists in some academic discourse, where univariate summaries eclipse genome-wide evidence, potentially reflecting institutional incentives against acknowledging heritable group differences. Edwards' framework, grounded in multivariate statistics, underscores that human diversity exhibits both continuous gradients and discrete aggregates, rendering blanket denial empirically untenable.[136]Racial Differences in Intelligence and Cognitive Traits
Observed differences in average intelligence quotient (IQ) scores persist across racial groups on standardized tests in the United States and internationally. In the US, meta-analyses of multiple datasets show White Americans averaging around 100, Black Americans around 85, Hispanic Americans around 89-93, and East Asian Americans around 105-106.[137][138] These patterns hold across diverse IQ subtests and achievement measures like the SAT, ACT, and NAEP, with gaps most pronounced on highly g-loaded (general intelligence) items that correlate strongly with overall cognitive ability.[137] The Black-White IQ gap of approximately 15 points (1 standard deviation) has narrowed modestly since the 1970s, from about 18 points to 10-15 points by the 2010s, but remains substantial, with Black Americans scoring below the White mean and overlapping minimally at the tails.[139] East Asian advantages over Whites, around 5-6 points, appear stable and are replicated in international assessments like PISA and TIMSS, where national averages align with racial ancestries.[137] These differences predict real-world outcomes, including educational attainment, occupational success, and socioeconomic status, independent of socioeconomic controls.[137] Twin and adoption studies indicate high within-group heritability of intelligence (50-80%) across racial groups, with no significant differences in heritability estimates between Whites, Blacks, and Hispanics.[140] This heritability rises with age and in higher-SES environments, suggesting genetic factors dominate individual differences once environmental variance is minimized.[137] Between-group gaps, however, cannot be fully explained by environment alone: transracial adoption studies, such as the Minnesota Transracial Adoption Study (1976-1986 follow-up), found Black children adopted into White upper-middle-class families averaging IQ 89 at age 17, compared to 106 for White adoptees and 99 for mixed-race adoptees, regressing toward racial group means despite shared enriched rearing.[137] Similar patterns emerge in French and Belgian studies of sub-Saharan African adoptees scoring 10-15 points below European norms.[137] Physiological correlates support a partial genetic basis for racial cognitive differences. Average brain volume, measured via MRI, follows the order East Asians (1,364 cm³) > Whites (1,347 cm³) > Blacks (1,267 cm³), correlating 0.40 with IQ across individuals and groups.[141] Simple reaction times and inspection times, less culturally influenced than IQ tests, show analogous racial hierarchies, with East Asians fastest, followed by Whites, then Blacks.[137] Evolutionary selection pressures, including colder climates favoring planning and impulse control in Eurasian populations, provide a causal framework consistent with these patterns, though mainstream academic consensus, influenced by institutional pressures against hereditarian views, attributes gaps primarily to socioeconomic and cultural factors despite weak empirical support from equalization experiments.[137][142] Anonymous surveys of intelligence researchers reveal 50% or more attributing at least half the Black-White gap to genetics, contrasting with public statements shaped by career risks in ideologically uniform fields.[142] Interventions like the Abecedarian Project yield temporary gains (4-7 IQ points) that fade by adolescence, underscoring limits of environmental remediation.[137] While no single gene explains group differences, polygenic scores from GWAS increasingly align with observed IQ variances within and between ancestries, bolstering causal realism over denialist fallacies equating within-group heritability with between-group causation.[143]Behavioral and Societal Outcome Disparities
Significant disparities in criminal offending rates persist across racial groups in the United States. According to Bureau of Justice Statistics data for 2023, the homicide victimization rate for Black persons was 21.3 per 100,000, compared to 3.2 per 100,000 for White persons.[144] FBI arrest data from 2019, the most recent detailed breakdown available, indicate that Black individuals, comprising approximately 13% of the population, accounted for 51.3% of adult arrests for murder and non-negligent manslaughter, while White individuals accounted for 45.7%.[145] These patterns extend to other violent crimes, with Black overrepresentation in arrests for robbery and aggravated assault.[145] Incarceration rates reflect these differences: in 2020, the imprisonment rate for Black U.S. residents was 938 per 100,000, substantially higher than for White residents at around 200 per 100,000, though the Black rate has declined 37% since 2010.[146] Black individuals represented 37% of the prison and jail population in recent years, despite being 13% of the general population.[147] Educational achievement gaps by race remain pronounced, as evidenced by National Assessment of Educational Progress (NAEP) scores. In 2022, average fourth-grade mathematics scores were approximately 241 for White students, 224 for Hispanic students, and 208 for Black students, with similar gaps in eighth-grade mathematics (White: 282, Hispanic: 260, Black: 247).[148] Reading scores showed comparable disparities: fourth-grade averages were 221 for White students, 205 for Hispanic, and 190 for Black students.[149] These gaps, equivalent to about one to two grade levels, persisted despite overall declines from pre-pandemic levels, with Black and Hispanic students experiencing steeper drops at lower proficiency percentiles.[148]| Racial Group | 4th Grade Math NAEP (2022) | 8th Grade Math NAEP (2022) | 4th Grade Reading NAEP (2022) |
|---|---|---|---|
| White | 241 | 282 | 221 |
| Hispanic | 224 | 260 | 205 |
| Black | 208 | 247 | 190 |