A detailed critique of the European academy's handling of African genetic data, particularly the work of Cavalli Sforza. With the Human Geonome Project rolling along at full speed, Scott McEachearn wonders whether the European academy be trusted to render a balanced picture. Among his criticisms is that data on African peoples is being analyzed in ways different from that accorded European samples, for example with a lesser level of detail in some analyses that masks the picture on the ground.
excerpt from: Scott MacEachern Genes, Tribes, and African History. Scott MacEachern. Current Anthropology Volume 41, Number 3, June 2000. p. 360-367
- African ethnic units are not bounded, homogeneous monoliths either frozen in place since before a.d. 1492 or caromming around the continent like culture-bearing billiard balls.
- A number of the groups used in the analyses in The History and Geography of Human Genes did not exist as such five centuries ago, and the modes of human interaction in Africa are not in any way reducible to a list of technological innovations and mass migrations. In part because of this lack of chronological control, the procedures used by Cavalli-Sforza et al. to associate genetic patterning with cultural events in the past are quite unsystematic, involving attempts to fit secondhand knowledge of archaeological, ethnographic, and linguistic reconstructions into a Procrustean bed of genetic patterning. Clark’s (1998) description of the “ransacking” of European genetic data for meaning applies equally well in the African case.
-Presumably, this patterning is explained by the admixture of “Caucasoid” and “Negroid” populations in northeastern Africa..
--These “Caucasoid” genetic contributions are thus invoked as the primary explanation for the variation exhibited in the first, second, and third principal components but seem to refer to different sets of genetic characteristics and thus presumably to different populations of “Caucasoids.” These interpretations would seem to lack much real explanatory value.
--The extent of this confusion of different data sources is made evident by a map (1994: fig. 3.9.3) that purports to show a pattern of Bantu expansion based upon archaeological data in which most of the linkages (between Nilotic-speaking peoples and Central-Western Bantu or between Bane populations and Northeastern Bantu, for example) are sustained by no archaeological data at all. No other mechanisms for genetic or linguistic dispersal are considered, and the con- nection of these different types of data seems quite unsystematic.
--Cavalli-Sforza et al. (1994:189–92) do not attempt to give historical explanations for African genetic frequency variation to the sixth principal component as they do for Europe.
-- The data given in this work indicate that such processes may be quite common on the African continent. In general, the correspondences between genetic relationships and those based upon linguistic and “tribal”/ethnic affiliation do not appear to be particularly close. Cavalli-Sforza et al.’s (1994:182–85) discussion of these correspondences abounds with perplexing relationships between different groups of people—Nubians with Moroccans, Ubangianspeakers with southwestern Bantu populations, Sara speakers of a Nilo-Saharan language with Hausa on the one hand and Biaka Pygmies on the other, and so on. The “Caucasoid” genetic affiliations of the San may prove to be another example.
--The Hausa, we should note, become Nilo–Saharans rather than speakers of Afroasiatic languages in the principal-component maps of Cavalli-Sforza et al.
-- Cavalli-Sforza et al. recognize the peculiarity of a situation in which one ethnonym encompasses two distinct genetic populations and respond by recalling Murdock’s (1959:414–15) distinction between pastoral Fulbe, who are supposed to be “Caucasoid-like,” and settled Fulbe, who are “Negroid.” They intimate that the Peul sample, which also contains genetic material from people identified as Tukolor, thus contains more admixture from “Caucasoid” (specifically Berber) populations. However, this well-known distinction between “cattle Fulani” and “town Fulani” is very frequently overdrawn..
-- the Wolof and Serer populations that cluster with the Peul are not particularly “Caucasoid,” and these westernmostWest African groups are certainly distinguished from Saharan populations according to Cavalli- Sforza et al.’s principal-component analysis (1994: 170).
--Indeed, historical data might lead us to expect such genetic results. This possibility seems to be comprehensively edited out of The History and Geography of Human Genes, presumably because European settlement in southern Africa took place after a.d. 1492. This claimed association of Khoisan people with “Caucasoids” is quoted in more recent works on genetics and history in Africa, among them the work by Passarino et al. (1998) on Ethiopian populations. This latter paper exhibits the same reliance upon inappropriate sources as does Cavalli-Sforza et al., with for example use of a 1964 Encyclopedia Britannica article as a primary reference on the prehistory of Ethiopia.
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"It is thus extraordinarily ironic that Cavalli-Sforza, Menozzi, and Piazza in their attempts to elucidate the ancient genetic history of the whole of humanity find it necessary to posit that Africans, as well as members of indigenous groups in other parts of the world, really have been people “without history” (Trevor-Roper 1965:9) since a.d. 1492. If anything, the continent of Africa, at least, has for the past 500 years suffered from a surfeit of history, not its lack. The relatively recent and closely connected developments of nationalism and colonialism have certainly generated a hierarchy of states, ethnies, and “tribes” that can command the loyalties of people living in different parts of the world today, but the extension of those units into the past is a proposition to be tested, not a given.
The recent creation of “tribal” identities is not the only process of ethnic-group definition in Africa that fails to accord with the assumptions made in The History and Geography of Human Genes. The mosaic of peoples described by Roderick McIntosh (1998; see also McIntosh 1993) in The Peoples of the Middle Niger: The Island of Gold appears to be of very long standing indeed, with roots ultimately to be located in the mid-Holocene, but the complex and evolving relations between different specialist communities convincingly depicted in that work bear very little resemblance to ahistorical, static models of African “tribes.” This mosaic of groups incorporated people of different language affiliations; it involved extremely sophisticated ritual, economic, and technological accommodations to a diverse and changing natural and cultural milieu; it allowed for processes of immigration, emigration, and population interchange. Such constellations of interacting groups can be found elsewhere in Africa as well, although probably none have been as intensively investigated and described as the Middle Niger populations. Interaction between peoples, in Africa and elsewhere, is a continuing and complex process and only rarely involves the spasms of mass migration that Cavalli-Sforza et al. invoke.
Modern concepts of ethnicity and the social groupings that result from those concepts seem if anything more closely comparable to the demes studied by population geneticists than to the “tribes” created by colonialists and ethnographers and adopted as units of study by Cavalli- Sforza et al. Demes are not necessarily held to have sharp boundaries, and intergrades between demes at particular levels are both clinal and common. Similarly, the exact characteristics of particular demes may be defined in reference to particular research problems. This somewhat resembles instrumentalist formulations that locate ethnic identities in situationally contingent bundles of social and cultural identifications that can assume differential importance in different social situations while simultaneously existing at multiple social and spatial levels (Barth 1969, Cohen 1978, Handelman 1977, Mc- Kay 1982). Ethnoarchaeological research by a number of investigators working in Africa (David 1992, Hodder 1982, Larrick 1986, MacEachern 1998, Wiessner 1984) has detected similar patterning in material culture. It is unlikely that such patterning would derive from the ahistorical monoliths identified as “tribes” by Cavalli- Sforza et al. (1994).
---------------------- MacEachern Genes, Tribes, and African History F 365. excerpt continued -------------------------------- quote: African Examples
As in each other continental area investigated, Cavalli- Sforza, Menozzi, and Piazza treat their data on African genetic variation in different ways and for somewhat different purposes. Trees of genetic distance and similarity are generated through average linkage analysis in order to elucidate phylogenetic relationships between modern populations and the histories of ancient fissioning that have resulted in those modern populations. Two-dimensional principal-component analyses of variation in genetic characteristics allow an alternative, graphic presentation of modern population affinities for comparison with the phylogenetic trees. Studies of the distributions of single alleles of particular genes yield data on (and allow speculation about) particular environmental adaptations and interactions between different human groups; these data are somewhat beyond the bounds of this paper. Finally, synthetic maps of each region are derived from the results of principal-component analysis of multiple gene frequencies—for 79 genes in the African case, for example. As in the European instance noted above, Cavalli-Sforza et al. usually assert that the spatial patterning of values for each principal component is a reflection of a specific population/language movement (again, the two are often not differentiated) in the past. I will first examine some features of the African genetic tree and principal-component map given in Cavalli- Sforza et al. (1994:169, 170) and then examine the synthetic maps of the continent. I emphasize that this inquiry is very far from being comprehensive, but I hope that it will be illustrative.
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Fig. 1. Genetic tree of 49 African populations (Cavalli- Sforza, Menozzi, and Piazza 1994:fig. 3.5.1; q1994, Princeton University Press, reprinted by permission of Princeton University Press). trees and principal-component analysis North African groups. The continental genetic tree of African populations generated by Cavalli-Sforza, Menozzi, and Piazza (reproduced here as fig. 1) uses genetic data from 49 human groupings in Africa. The most fundamental differentiation shown is that between sub-Saharan Africans, on the one hand, and Saharan and Northern African populations, on the other. It is among the latter group (16 of the 49) that we see the only national identifications of populations (Algerians, Sudanese, Moroccans, Tunisians, Libyans, Egyptians), whereas, as noted above, such identifications are the rule across the Mediterranean in Europe. The other Saharan/ Northern African and all the sub-Saharan population samples identified are denoted by (1) “traditional” ethnonyms (Amhara, Hausa, Sandawe, and so on), (2) geographical designations (Bantu, N.E., Bantu, S.W., and so on), (3) designations based on language affiliation (Nilotic, Ubangian, Volta, San), or (4) designations based on particular physical characteristics (Pygmy/“Pygmoid”). As noted above, appendix 3 makes the human diversity of many of these samples obvious.
Within the Saharan/Northern African group there are two subclusters. One is comprised of a number of “national” North African populations (Moroccan, Tunisian, Libyan, Egyptian), as well as Nubian, Bedouin, Berber, and Canarian. Cavalli-Sforza et al. (1994:172) note that there are few data available on the genetic makeup of the Canarian group, and it is not clear whether they are data on modern peoples or on the extinct Guanches. The other cluster consists of a number of Northeast African populations, including the national Sudanese and a generalized Cushitic-speaking group. Within this Northeast African group, one subcluster does not conform to historical or linguistic expectations, as it associates the Algerian national population fairly closely with the Beja of eastern Sudan and somewhat more distantly with the Berber-speaking Tuareg; the latter group thus appears to be rather distinct from other Berber populations. Cavalli- Sforza et al. (pp. 172–73) posit an ancient relationship between Tuareg and Beja, largely, it appears, on the basis of their shared status as pastoralists. There are no other data that I know of that indicate such a link, and in any case it does not explain the putative close relationship of modern Algerians to both groups. The researchers note that they have data on relatively few genes from this Algerian group, but it should be pointed out that such small data sets are no obstacle to the acceptance of particular genetic associations when these fit their expectations— the Canarian case noted above is a good example.
This pattern of acceptance and rejection of generally equivalent data on the basis of their concordance with expectations is common throughout The History and Geography of Human Genes and is an example of the strategy of post-hoc accommodative argument noted by Clark (1998).
The distinction between Saharan/Northern African populations and peoples living in sub-Saharan Africa is explained by the varying contribution of genes from “Caucasoid” populations in Europe and Southwest Asia to the former. This is very likely a contributing factor, given the archaeological and historical evidence of such population interactions around the Mediterranean. It is also quite likely that clines in gene frequencies across the Sahara are in part the result of natural selection operating upon characteristics that are not adaptively neutral in the very different environments through this region. There is a significant amount of evidence for both climatic and latitudinal effects upon different gene frequencies (Cavalli-Sforza et al. 1994:143; Mastana, Constans, and Papiha 1996; O’Rourke, Suarez, and Crouse 1985; Spitsyn et al. 1998). The greater instability of Saharan environments through time probably offered less scope for such in situ adaptation than is the case among, for example, the Nile Valley populations examined by Brace et al. (1996).
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Saharan and Sahelian groups (various Berber- and Arabic- speaking populations, including Tuareg and groups subordinated to them, such as the Bella and the Haratine and Saharan-speakers such as the Chaamba, Reguibat, Teda, and Kanembu) are not covered in detail in the work (Cavalli-Sforza et al. 1994:173), although investigations of biological variation among those populations have indicated that their anthropometric and genetic affiliations are very diverse and complex (Froment 1999). This lack of data on intermediate groups may make human physical and genetic distinctions across the Sahara appear more clear-cut than they are. The status of these populations is particularly important given that climatic change rendered significant parts of the Sahara passable (and in some cases habitable) through periods in the Holocene at least, with the result that there is abundant evidence of more extensive human contacts across the desert than have existed in historic times. Sutton (1974) and Ehret (1993) have suggested that the Saharo-Sudanese Neolithic tradition was largely the province of Nilo- Saharan-speakers. Populations speaking those languages do not, however, occupy an intermediate position between North African and sub-Saharan African populations, suggesting that either the correlations between archaeology and linguistics or those between genetics and linguistics—or both—are erroneous.
While Cavalli-Sforza et al. emphasize the contribution of immigrant genes to the modern genetic makeup of Saharan/Northern African populations, they do not really consider the possibility of an African genetic contribution to either Europe or the Near East. It thus appears that Africa accepts genetic contributions from other areas but does not reciprocate them. A principalcomponent map of 42 world populations (Cavalli-Sforza et al. 1994:82) indicates a somewhat more complex picture, with a succession of Basques, Sardinians, Near Eastern populations, and Berbers occupying a space intermediate between African and European populations, although certainly arrayed closer to European groups. This assumption is also at variance with the known history of the region, where we see evidence for two-way relations throughout the Holocene, especially via Southwest Asia and the Iberian and Italian peninsulas. People from North, Saharan, and sub-Saharan Africa have crossed the Mediterranean as settlers, conquerors, and slaves through recorded history just as have Europeans. In recent times such population flows may have tended to be from north to south, but it should not be assumed that this has always been the case.
Pygmies, Khoisan, and Caucasian connections. The high-level cluster of sub-Saharan African populations contains 33 of the 49 populations of the phylogenetic tree. It is a considerably more diverse grouping than the Saharan/Northern African, with multiple subclusters at different fissioning points. The most famous “outlier” populations of traditional African ethnography are of course Pygmy and Khoisan-speaking groups, which are to varying degrees physically distinct from their African neighbors and also to varying degrees participate in foraging economies. These latter are frequently seen by Westerners as archaic, and Pygmy and Khoisan populations have often been identified as unchanged relics of earlier ages (e.g., Thomas 1959:6–8;Turnbull 1983:11–13, 157–58). Pygmy (Mbuti and Biaka) and “Pygmoid” populations are found at various points on Cavalli-Sforza et al.’s phylogenetic tree as outliers and with other groups. As Froment (1998) points out, this separation of Pygmy and other African populations is extremely imprecise; it depends to a great extent upon linguistic criteria, ignores the numerous transitional populations (not only those denominated as “Pygmoid”), and systematically discounts the fact that we know very little about the historical and physical relations between these groups over any significant period of time.
---------------------- MacEachern Genes, Tribes, and African History .. . excerpt continued -------------------------------- Similarly, Khoi and San populations cluster with a Somali sample (which itself is held to be out of place, given that Somali groups geographically sit within the Northern African range), while Sandawe clusters with populations from Senegambia and Hadza is an outlier between the two. Cavalli-Sforza et al. (1994:169–70, 174–77, 189–93) posit that especially San populations are the result of admixture between “Caucasoid” groups originating in Southwest Asia and African “Negroid” groups. This is supposed to be a different process of interaction across the Red Sea from the one that yielded the distinctive genetic and physical characteristics of Ethiopian populations; indeed, the San and Ethiopian peoples are held to be “similar to Caucasoids but . . . otherwise very different [from one another]” ( p. 191). The historical mechanisms—and even the demographic meaning—of such multiple similarities are left unspecified. This is unfortunate, given that hypotheses of immigration into Africa by (often “Hamitic”) “Caucasoids” have bedeviled African history and archaeology for much of the past century, often being advanced to explain away African cultural innovations and based on very unsatisfactory evidence. One would have hoped that consciousness of this situation would have led the authors of The History and Geography of Human Genes to substantiate this hypothesis in detail.
The nongenetic evidence marshaled in support of the hypothesis of relations between San groups and populations in the Near East is extremely weak. A putative “Asian” genetic contribution to forager groups in Ethiopia (Nijenhuis and Hendrikse 1986) is discussed only with reference to “Pygmoid” populations, although Cavalli- Sforza et al. (1994:174) imply that these groups are related to the San. They claim ( pp. 160, 176) that skeletal material “credibly identified as San” has been found in various parts of North and East Africa, including northern Egypt, but note only parenthetically that this assertion in Nurse, Weiner, and Jenkins (1984) is based upon a 30-year-old paper by Philip Tobias (1968 ). The Tobias paper does not in fact seem to make that claim, and it is in any case disputed by more recent researchers on the basis of the characteristics of the material involved, the very fragmentary state of the collections, and known problems with the accumulation of Khoi and San skeletal reference collections (Froment 1998; Morris 1986, 1987; Rightmire 1975; 1984:193–98; Schepartz 366 F current anthropology Volume 41, Number 3, June 2000 Fig. 2. Principal-component analysis of 49 African populations. BNT, Bantu and Bane; C, Central; ETH, Ethiopia; KH, Khoisan; N, North Africa; NS, Nilo-Saharan; PG, Pygmies; W, West Africa (Cavalli-Sforza, Menozzi, and Piazza 1994:fig. 3.5.2; q1994, Princeton University Press, reprinted by permission of Princeton University Press).
1988). In fact, the identification of this skeletal material from northeastern Africa as related to San skeletal material from southern Africa is very doubtful; the material indicates that ancient populations in the area were most closely affiliated with the present-day inhabitants. The only widely accepted evidence of ancient Khoisan populations in East Africa is the ascription of the Sandawe and Hadza languages to the Khoisan phylum (with even less well-attested traces of Khoisan contacts in Dahalo and Yaaku [Ehret 1974:11, 88]). However, the Khoisan affiliations of Sandawe and/or Hadza are still disputed by some linguists, and in any case the available genetic data do not indicate a close relationship between Sandawe and Hadza people, on the one hand, and San and Somali people, on the other. The paradox is obvious: Sandawe and Hadza provide the only firm link between San populations and northeastern Africa (a linguistic one), but according to the genetic data that provide the basis for The History and Geography of Human Genes they are more closely related toWest and Central African groups (fig. 2). There seems to be no a priori reason to associate Khoisan-speaking populations with Southwest Asia on the basis of San genetic data and not to associate Khoisan-speaking populations with Senegambia on the basis of Sandawe genetic data, but this is just what Cavalli- Sforza et al. do. It is also, of course, possible that either or both associations are spurious, especially given the small size of some of these forager groups and the attendant possibility of genetic drift.
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We must remember, as well, that the southern tip of Africa is not in fact occupied only by Khoisan and other African peoples, as the discussion in Cavalli-Sforza et al. (1994:158–68) would sometimes seem to imply. It is also the only part of the continent to have seen extensive settlement by Europeans (and Asian people arriving in the context of colonization) over the past four centuries. This has certainly involved a considerable amount of genetic interchange between indigenous and immigrant populations, along with the formation of a number of communities of mixed descent, with genetic, cultural, and linguistic affiliations to Khoisan, other African, European, and Asian groups. These communities and their origins are discussed at some length in Nurse, Weiner, and Jenkins (1985:221–40); they have at various times and in various areas included !Kora, Baster, Orlam, Gyzikoa, Griqua, and “Cape Coloured” populations, among others, and have occupied territories in South Africa, Namibia, and Botswana. As Morris (1992, 1997) points out, “Caucasoid” genetic and morphological features seem to be less important among Griqua populations (the only cases that I know of for which these affinities for these groups have been studied) than might have been expected on historical grounds, but these groups are quite diverse, and rather little is known of genetic exchange between European and African populations on the frontiers of European settlement in southern Africa.
It would seem reasonable to seek evidence for “Caucasoid” genetic affiliations among southern African populations in this recent and relatively well-attested contact situation rather than in putative Khoisan contacts with Northeast Africa and Southwest Asia for which no firm evidence exists. Indeed, historical data might lead us to expect such genetic results. This possibility seems to be comprehensively edited out of The History and Geography of Human Genes, presumably because European settlement in southern Africa took place after a.d. 1492. This claimed association of Khoisan people with “Caucasoids” is quoted in more recent works on genetics and history in Africa, among them the work by Passarino et al. (1998) on Ethiopian populations. This latter paper exhibits the same reliance upon inappropriate sources as does Cavalli-Sforza et al., with for example use of a 1964 Encyclopedia Britannica article as a primary reference on the prehistory of Ethiopia.
West African cases. As noted above, the Sandawe sample clusters with samples from westernmostWest Africa, specifically from Serer, Wolof, and Peul populations. It was this latter group that first caught my attention when I looked at Cavalli-Sforza et al.’s phylogenetic tree because of the distinction between the Peul and Fulani samples that I have mentioned. These two ethnonyms both denote Fulbe people, but the Fulani sample is closely associated with a set of samples from Nigerian populations, including Ibo, Yoruba, and Hausa—groups a long way from Senegambia. Cavalli-Sforza et al. recognize the peculiarity of a situation in which one ethnonym encompasses two distinct genetic populations and respond by recalling Murdock’s (1959:414–15) distinction between pastoral Fulbe, who are supposed to be “Caucasoid-like,” and settled Fulbe, who are “Negroid.” They intimate that the Peul sample, which also contains genetic material from people identified as Tukolor, thus contains more admixture from “Caucasoid” (specifically Berber) populations. However, this well-known distinction between “cattle Fulani” and “town Fulani” is very frequently overdrawn (for other considerations of the issue, see e.g., Curtin 1975:19–22; Irwin 1981:46–55; Schultz 1981), the Wolof and Serer populations that cluster with the Peul are not particularly “Caucasoid,” and these westernmos tWest African groups are certainly distinguished from Saharan populations according to Cavalli- Sforza et al.’s principal-component analysis (1994: 170).
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It is more likely that this distinction between the populations recorded as Fulani and Peul can in great part be traced to social/political processes over the past 200 years in West/Central Africa, where among other events the jihad of Uthman dan Fodio led to the establishment of the Sokoto Caliphate in modern Nigeria and Cameroon and to an attendant favorable change in the status of a Fulbe ethnic identity. Under these circumstances, we would expect that many indigenous people, especially those of Hausa background but also including members of other Nigerian and Cameroonian societies, would attempt to assimilate to that Fulbe identity. Indeed, such processes are often discussed and debated in the Nigerian historical literature (Salamone 1985, Smith 1997) and can probably be seen in play in the mixed ethnic affinities of the “Fulani” sample in appendix 3 of The History and Geography of Human Genes (Cavalli- Sforza et al. 1994:470).3 Difference between “Peul” and “Fulani” thus appears to be not the result of a longstanding division of two populations subsumed under one ethnonym but quite the opposite—the relatively recent creative manipulation of identity for political and social advantage.
The significance of this conclusion lies not so much in the ethnographic concepts used by Cavalli-Sforza et al. as in the possibility of such a drastic change in lin- 3. The Hausa, we should note, become Nilo–Saharans rather than speakers of Afroasiatic languages in the principal-component maps of Cavalli-Sforza et al. (1994:170, 181; see fig. 2) and “elongated” pastoral nomads a` la Hiernaux in the conclusions to the chapter on Africa (p. 194). These incorrect ascriptions indicate the difficulty, especially for nonspecialists, of working with such very large ethnographic and linguistic data sets. This difficulty probably also accounts for citations of, for example, works dealing with Chukotskii and Brazilian populations in references to African groups (p. 471).
linguistic and ethnic affiliation by a significant group of people in less than two centuries. If such a change happened in northern Nigeria, how common is it elsewhere, and how many such changes affect the analyses in The History and Geography of Human Genes? The data given in this work indicate that such processes may be quite common on the African continent. In general, the correspondences between genetic relationships and those based upon linguistic and “tribal”/ethnic affiliation do not appear to be particularly close. Cavalli-Sforza et al.’s (1994:182–85) discussion of these correspondences abounds with perplexing relationships between different groups of people—Nubians with Moroccans, Ubangianspeakers with southwestern Bantu populations, Sara speakers of a Nilo-Saharan language with Hausa on the one hand and Biaka Pygmies on the other, and so on. The “Caucasoid” genetic affiliations of the San may prove to be another example.
Technological innovations, population expansions, and especially migrations are invoked to explain as many of those relationships as is possible, but these explanations often seem ad hoc. For example, archaeological and linguistic data involving the Bantu expansion are invoked to explain the apparently very close genetic relations between northwestern and southeastern Bantu populations. Surely, however, any such explanation should also account for the relative lack of genetic similarity of the intervening Bantu populations (table 1). In any case, the close relations between archaeological and linguistic reconstructions (the former very dependent upon the latter) in this case vitiate their separate use as independent tests. Indeed, Vansina (1995) has cogently critiqued the assumptions that there are close parallels in archaeological and linguistic data bearing upon the expansion of Bantu languages and that that expansion was the result of a single, massive migration process. The archaeological and linguistic data simply do not yield the neat, uncomplicated picture of the past that Cavalli-Sforza et al. present. The extent of this confusion of different data sources is made evident by a map (1994: fig. 3.9.3) that purports to show a pattern of Bantu expansion based upon archaeological data in which most of the linkages (between Nilotic-speaking peoples and Central-Western Bantu or between Bane populations and Northeastern Bantu, for example) are sustained by no archaeological data at all. No other mechanisms for genetic or linguistic dispersal are considered, and the con- nection of these different types of data seems quite unsystematic.
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Synthetic maps of african genetic variation
Cavalli-Sforza et al. (1994:189–92) do not attempt to give historical explanations for African genetic frequency variation to the sixth principal component as they do for Europe. (Perhaps they would have done so if there were as many different regional historical reconstructions for Africa as there are for Europe.) Instead, they limit their explanations to the first four principal components, which encompass about the same percentage of total variance as in the European case. The synthetic map derived from the first principal component (fig. 3) has a strong north-south gradient, with opposing extremes along the Mediterranean coast and from the Equator southward. The researchers relate this to the ancient presence of “Caucasoid” populations along the northern coast of Africa and the gradual admixture of “Caucasoid” and “Negroid” populations across the Sahara. They also comment upon the paucity of data on Saharan populations. As noted above, we should remember that this gradient is also an environmental one and that it is quite likely that environmental variability is affecting the genetic makeup of African populations to some degree.
The discussion of patterning on the synthetic maps for the second and third principal components is rather confusing. Cavalli-Sforza et al. (1994:189) note that both maps show maximum values in northeastern Africa, although the specific association with Ethiopia is not as clear as they claim. They state that the map of the second principal component indicates a similar set of maximum values in the area of southwestern Africa occupied by Khoisan-speakers in precolonial times and that this indicates that there existed a population ancestral to modern Khoisan peoples somewhere near Ethiopia. Low values on the second principal component in the areas intervening between Ethiopia and the Kalahari are ascribed to the later settlement of those areas by Bantu peoples. The maps (figs. 4 and 5) actually indicate that this pattern is based upon variation in the third principal component. The difference is significant, given that the second principal component explains 18.6% of the total variance and the third only 10.3%, but the text seems to indicate that this pattern is in fact associated with the second.
Presumably, this patterning is explained by the admixture of “Caucasoid” and “Negroid” populations in northeastern Africa that Cavalli-Sforza et al. believe gave rise to the Khoisan peoples. However, the maps for the second and third principal components show almost opposing values along the Mediterranean coast, where the presence of “Caucasoid” groups is held to be the explanation for the patterning of the first. Similarly, northeastern and southwestern Africa show maximum divergence on the third principal component, which is accounted for by their differences from one another in a context of general relationship to “Caucasoid” groups. These “Caucasoid” genetic contributions are thus invoked as the primary explanation for the variation exhibited in the first, second, and third principal components but seem to refer to different sets of genetic characteristics and thus presumably to different populations of “Caucasoids.” These interpretations would seem to lack much real explanatory value.
The fourth principal component accounts for only 7.0% of the total variance (fig. 6). Maximum values are associated with the northwestern part of the Central African tropical forest and minimum values with the border regions of Mali, Niger, and Burkina Faso. Parsimoniously, the researchers associate these maximum and minimum values with two different agricultural expansions. They associate the area of maximum values with an expansion of Bantu populations, although one might associate the patterning with Adamawa-Ubangian groups as well (David 1982:88–91; Saxon 1982) and the influence of this massive Bantu migration upon genetic variation would seem to be extraordinarily low compared with that of the “Caucasoid” gene flows that have determined the nature of the first three principal components. They admit that there is no equivalent evidence for an agricultural expansion from the area of minimum values in the West African Sudanic zone but counsel future comparison with archaeological data. These syn- thetic maps sometimes appear to function as historical Rorschach tests, with genetic data being associated with ancient cultural processes on the basis of general resemblances in spatial patterning.
The History and Geography of Human Genes is an extraordinary compendium of information on human genetic variation. It links a huge amount of data on that variation with archaeologically, historically, and linguistically known cultural processes that took place at various times and in various areas. Its hypotheses have been provocative and in many cases useful, and researchers in other fields have responded to them in ways that will eventually increase our knowledge of our shared human past. In the long run, Cavalli-Sforza et al. have probably established the examination of patterns in genetic characteristics as a valuable complement to older, more established avenues for the examination of prehistory. This genetic research was limited by the lack of samples from many areas, by the necessity of using samples collected under very different conditions, by the great variation in the amount of information available on the composition of the groups being sampled, and by the lack of availability of statistical techniques that could account for interactions between groups during the process of constructing phylogenetic trees. To their credit, Cavalli-Sforza, Menozzi, and Piazza recognize and highlight a number of these problems and try to compensate for them. Their solutions are often sophisticated and ingenious, and the potential of these techniques is obvious.
The danger for African archaeology is that the very impressive amount of genetic data amassed in The History and Geography of Human Genes will convince nonspecialists of the validity of the hypothesized associations between human groups. That would be unfortunate, because this pioneering synthesis is hobbled by a conceptual model of human behavior that takes little account of ethnographic, historical, linguistic, and archaeological research on the constitution of human societies and of the various ways in which cultural meaning is constructed in the continuing negotiation of individual and group identities. Similarly, the discussion of relations between language and ethnicity pays virtually no attention to linguistic analyses of such relationships. Their compilation of the data that make up the African sample should have indicated to the researchers that these relations are extremely complex, while the varying criteria—linguistic, geographic, national—used for identifying populations make it seem unlikely that the groups under study are comparable entities.
African ethnic units are not bounded, homogeneous monoliths either frozen in place since before a.d. 1492 or caromming around the continent like culture-bearing billiard balls. They are dynamic entities, manipulated in response to changes in the natural and social environment, and their composition can change very quickly indeed. Differences in the temporal resolutions of genetic, linguistic, archaeological, and historical analyses are one of the main difficulties in these multidisciplinary studies, and the ability to control chronologies is more restricted in the former two disciplines than in the latter. It is often difficult, therefore, to establish whether the genetic patterning exhibited by modern populations can be traced back to events that happened centuries or millennia ago. A number of the groups used in the analyses in The History and Geography of Human Genes did not exist as such five centuries ago, and the modes of human interaction in Africa are not in any way reducible to a list of technological innovations and mass migrations. In part because of this lack of chronological control, the procedures used by Cavalli-Sforza et al. to associate genetic patterning with cultural events in the past are quite unsystematic, involving attempts to fit secondhand knowledge of archaeological, ethnographic, and linguistic reconstructions into a Procrustean bed of genetic patterning. Clark’s (1998) description of the “ransacking” of European genetic data for meaning applies equally well in the African case.
The deme concept, often used in population genetic research in other species, would seem to be a better and more flexible fit for the study of human genetic variation mac eachern Genes, Tribes, and African History F 371 than “tribal” typologies borrowed wholesale from ethnographic research done 50 or more years ago, especially since it seems to find resonances in some more recent concepts of ethnicity. It remains to be seen whether it will be applied to human genetic research in Africa and elsewhere. It would be interesting to see, for example, whether human demes on some level correspond to the material distributions that we call archaeological traditions, without any attempt to fit either genetics or archaeology to the straitjacket of the ethnographic “tribe.” Archaeological distributions of artifacts frequently occur over much larger territories than do the ethnic (“tribal”) units that ethnographers study in the present, and it is possible that in some cases this reflects movements by artifact producers, especially women, that would also be reflected in patterns of genetic variation (MacEachern 1998). In general, research on the African past would at this point benefit far more from small-scale studies of genetic patterning within and between particular communities than from the continental and subcontinental approaches that make up The History and Geography of Human Genes.
The genetic data available for Africa have serious limitations, but the patterns of variation demonstrated by these data are interesting and probably do indicate patterns of cultural interaction in the past. There are, however, good reasons to be suspicious of efforts to correlate those patterns with cultural processes at the level of specificity attempted by Cavalli-Sforza et al. The project of correlating the data from these different kinds of investigation still lies well before us, and it would be a great mistake to assume that such correlations will be self-evident. Research that has as its goal the study of the history and geography of human genes in Africa and elsewhere must be truly interdisciplinary, working with the best knowledge of other disciplines that can be acquired. A study that uses the terminology of other disciplines but takes insufficient account of the concepts behind that terminology risks generating misleading reconstructions of human history and prehistory. ============
KEITA WEIGHED IN:
s . o. y. keita 1925 2nd St., N.W., Washington, D.C. 20001-1667, U.S.A. 30 xi 99 mac eachern Genes, Tribes, and African History F 375 --------------------------------------------------
MacEachern has given us an effective critique of the African chapter in Cavalli-Sforza et al.’s book, while also illustrating general theoretical problems in syntheses of archaeology, ethnicity, linguistics, and human biology. The insights offered are especially useful for those interested in Africa, for which scholarship has long been hampered by myths and stereotypes. Notable among these is a paradigm which sets limits on authentic biocultural indigenous Africanness; this surprisingly persists in some scientific literature. The work of even some Africanists is still influenced by this legacy, which usually manifests itself around the problematic construct of race. Although MacEachern has given a cogent presentation, there are a few concerns.
One wishes that emphasis had been placed on the African origin and differentiation of the Afro-Asiatic language family and its subsequent spread to Asia (Greenberg 1966; Bender 1975; Diakonoff 1965, 1981; Ehret 1984, 1995; Ruhlen 1991). The dubious Nostratic construct has been used to postulate the spread of food production into Africa (from Asia) by Afro-Asiatic-speakers. Significantly, reconstructed common Afro-Asiatic has no terms for food production (Ehret 1984, 1995) and is accorded the same time depth as Nostratic (cf. Ehret 1984 and Barbujani and Pilastro 1993). Furthermore, most Nostraticists now conceptualize Afro-Asiatic to be a sister to Nostratic, not a daughter (Ruhlen 1991). Finally, archaeological data support migration from Africa into the Near East during the time frame suggested by some Nostratic models for immigration into Africa (cf. Bar- Yosef 1987 and Barbujani and Pilastro 1993).
On a technical note, MacEachern has made a common error, that of easily equating phenetic similarity with a necessary genealogical relationship. The results of mathematical techniques employed by human biologists must be interpreted with sound biological principles and other information (Rhoads 1984, Harrison 1984). The fact that small samples of Beja and Algerians and then of Nubians and Moroccans cluster clearly cannot be taken as necessarily indicative of a close genealogical relationship. The similarity may have many explanations including chance, especially since, as MacEachern notes, the nature of any links between earlier and later peoples having these designations remains an open question.
This is even more so when selection, migration, gene flow, and language shift have to be integrated into explanatory models. Harrison (1984:61), considering the results of simulations which evaluate interpopulation gene flow with and without selection, points to another important issue concerning migration and population affinities: the causes of inter-population patterns of gene frequency variation, and the meaning of affinities based not on ancestry but on genetic similarity. Clearly with varying levels of selection, populations which are genetically similar may have a much more remote common ancestry than populations which are genetically more different.
The lack of criticism on this point does not, however, seriously weaken the overall critique.
In fact, there is little to quibble with in MacEachern’s effort. However, he is perhaps somewhat overconfident in the belief that genetic research has led to the “dismemberment” of racial taxonomies and racio-typological thinking. While few write today in terms of Nordic or Jewish races, and this is a result of research and the World War II experience, there is still plenty of work on Africa which constructs its interpretations of diversity explicitly or implicitly in terms of conceptually idealized “Caucasoid” and “Negroid” “taxa,” implying a causal or foundational linkage between morphological complexes and a variety of genes.
Cavalli-Sforza et al.’s book is one example of this kind of work at some level. For some reason MacEachern does not directly engage its underlying nonevolutionary raciotypological model of interpretation or its use of racial terms, which are ontologically misleading in that they imply that supra-Saharan Africans were originally European- derived. These people supposedly interacted with “Negroids” and others, receiving some genes but contributing a lot more and thus becoming the primary explanation of African diversity. MacEachern’s critique would be even more useful if he had pointed out that
(1)fossils indicate the presence of anatomically modern people in supra-Saharan and Nile Valley Africa at a time when hominids in Europe had Neanderthal morphology;
(2) coalescence (and therefore differentiation) times for numerous genes sampled globally from living humans date to a period when modern morphology had not yet emerged or was to be found only in Africa; and
(3) global genetic diversity seems largely to be a subset of that found in Africa. (Whether this dates back to the time of Homo erectus or modern H. sapiens matters little; the diversity denoting the mythical “racial divergence” exists in Africa, as should be expected, and antedates the existence of the morphologies used to define races.) MacEachern fails to make these points, which together indicate that the African genetic profiles and morphologies being interpreted as solely resulting from European (or Southwest Asian) colonization and/or admixture (with “Negroids”) are largely the product of various authentic intra-African biohistorical processes which perhaps date to a time before there were any anatomically modern Europeans.
However, the Holocene climatic fluctuations of the Sahara (Hassan 1988), probable Late Pleistocene (and Holocene) population increase in response to changing subsistence regimes (Wetterstrom 1993), and the spread of early Afro-Asiatic-speakers from the Horn surely also had some effects. Supra-Saharan Africa is not primarily a product of extra-African colonization. There are many ways to be biologically African— many morphological combinations and genes (Hiernaux 1974, Keita and Kittles 1997).
The frequency of neutral private alleles of the right date and demonstrably originating outside of continental Africa will have to be determined before the non-African contribution to Africa’s genetic picture can be fully assessed. MacEachern seems to accept the racio-typological model of explanation at the larger level. Nevertheless, he contributes to the paradigm shift in understanding African biological variation, which will reject racio-typological thinking and use the reality of indigenous African diversity as an analytic tool.
======================================== OTHER COMMENTATORS WEIGHED IN: QUOTE:
alan g. morris Department of Anatomy and Cell Biology, University of Cape Town Medical School, Observatory 7925, South Africa (email@example.com). 17 xi 99
"MacEachern’s other major complaint about the compendium by Cavalli-Sforza et al. is the use of principal components to generate synthetic maps which are then interpreted as signs of specific past events. The principal components are not events. They are mathematical relationships and as such as far too complex to be given simple historical interpretations. MacEachern, in line with Clark’s (1998) assessment, accuses Cavalli-Sforza et al. of having a “pattern of acceptance or rejection of generally equivalent data on the basis of concordance with expectations.” Simplified, this means that they saw what they wanted to see. I entirely agree with Mac- Eachern’s concern that many students of anthropology, genetics, and history are going to take Cavalli-Sforza et al.’s work at face value. By doing that, they may be uncritically reproducing interpretations of the nature of ethnic identity into account.
This is not the first time that I have looked at the difficulties in interpreting genetic data. The equivalent genetic history of southern African people was published by Nurse, Weiner, and Jenkins in 1985. Again, the work was a wonderful production of data on a wide range of peoples, but the authors’ attempts at linking what they saw in the genes with history were sometimes very wide of the mark. Social theory and social events are not easily explained by biology. As does MacEachern here, I ended my comments by warning of my great fear “that students of archaeology, genetics and physical anthropology will simply assume that this is the academic ‘bible’ on the subject and will absorb many of the speculative passages without criticism” (Morris 1988:5).
Posts: 5107 | From: The Hammer | Registered: Aug 2008
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Hmmm nice big graphic^ me like em big pretty colors and stuff that looks like grapes or brain matter of aliens..and have not A thing to do wid topic posted about Cavalli-Sforza debunked.
Posts: 6546 | From: japan | Registered: Feb 2009
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quote:Originally posted by Brada-Anansi: Hmmm nice big graphic^ me like em big pretty colors and stuff that looks like grapes or brain matter of aliens..and have not A thing to do wid topic posted about Cavalli-Sforza debunked.
Apparently you didn't read or if you did comprehend the topic, and "stuff that looks like grapes or brain matter of aliens...", only to the ignorant.
Wow Brada you're easily impressed. You're sold on a 10 yr old study that claims to debunk a 16yo one. Do you know what confirmation bias means? I have some swamp land to sell, are you interested?
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^ Since you can't change the size of the graphics to make them easier to read, I'll just have to go from what I am able to make out that they merely make the mistake of identifying certain lineages as Eurasian when in fact they are of African origin since that is apparently your M.O.
To Zarahan, what Scott MacEachern shows is simply a rehashing of old prejudices into new science. Nothing more, nothing less. Such prejudices go back to the days of "true negroes" "Hamites" "Hamito-negroid hybrids" etc. etc. Only that these so-called 'experts' now use genetic labels. This is why we have their followers like Non-Thinker above thriving off this nonsense.
Posts: 23494 | From: Atlanta, Georgia, USA | Registered: Feb 2005
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"Sex rears its head again and again in the discussion, with much of the information on comparative sexual performance based on "self-assessment." Rushton is obviously much taken with the "salience of... buttocks and breasts" (pp. 167, 231) as measures of sexuality, although there is a dearth of objectively collected data. More telling is his evident fascination with the "Negroid" penis as an index of "potency" and libido. In his earlier publications on these matters, his information came from "self-assess- ment," but he has bolstered the "conclusions" at which he had previously arrived by reference to the alleged "data" gathered by a 19th-century figure identified only as a "French Army Surgeon."
--CL Brace. Review: Racialism and Racist Agendas Race, Evolution, and Behavior: A Life History Perspective by J. Philippe Rushton
Source: American Anthropologist, New Series, Vol. 98, No. 1 (Mar., 1996), pp. 176-177
^ You can add Dienekes and Mathilda to the list of those debunked as well as their cronies. Perhaps NonProven suffers from the same neurosis as Phillip Rushton-- perhaps the object of his fear is ultimately his greatest desire-- the black phallus.
This is why when it comes to Egypt, he just wants to...
Again and again, white writers note the greater length of the negro, and warn that white women would find sex painful, due to more powerful negro equipment. Others note however that such warnings may have been merely scare tactics by the insecure- to help discourage white women from sexual activity with the more potent black males. QUOTE:
"One of the distinctive traits of the Ethiopians [negroes], according to Serres, is the length of his penis, compared to that of the White man's organ. Its dimension is presumably commensurate with the excessive length of the vaginal canal of the Ethiopian [negro] woman. Both phenomena apparently have to do with the peculiar configuration of the pelvis of Black people. "From this particular physical make-up", Serres continues, "it ensues that the union of a Caucasian man and an Ethiopians woman is easy, without discomfort to the woman. Such is not the case with the union of an Ethiopian man and a Caucasian woman. The act is painful to the woman;" --Joseph-Anténor Firmin, Asselin Charles. 1897. The equality of the human races
One experienced European physician with extensive travel abroad, notes the negro lengths, and correlates size with buttock width- a marker noted in modern studies QUOTE: It is known however that the negro's member is much greater than that of other races. During the years that I practised as a doctor in South America I have verified this completely. This greater volume of the member of the man, corresponds with a greater width of the parts of the negroes. --Paolo Mantegazza. 2001. (re-issue) The Sexual Relations of Mankind
More powerful and developed Negro gluteus correlates with penis size one current study claims. Flat buttocks of Caucasians may lack this correlation
The supposed relationship between penile length and gluteal size may have a scientific basis, but contrary to belief, large buttocks is more predictive of longer penile length than small buttocks." -- Orakwe JC, et al. Show all. Can physique and gluteal size predict penile length in adult Nigerian men?. West Afr J Med. 2006 Jul-Sep;25(3):223-5.
Measurements and observations of a French surgeon in the colonial era testify of superior Negro endowment, compared to whites.
"Even when flabby, the Negro's yard still retains a size and consistence that are greater than that of the European, whose organ shrivels up and becomes soft and limp. The average size of the penis generally appeared to me to be about 7 3/4 to 8 inches in length, by two inches in diameter. Except with young lads, just arrived at the age of puberty, the penis is rarely less than 6 1/2 inches in length.. I took these measurements from the Sharpshooters, amongst whom I met specimens of the most of the races of Senegal and the Upper Niger. I often came across a penis of 9 3/4 to 10 inches by 2 1/4 inches, and once, in a young Bambara, barely twenty years of age, found a monstrous organ 11 3/4 inches long by 2.6 inches in diameter at the circular circumcision mark... I find in Mantegazza and exact confirmation of what I have just said." --Jacobus, X. Untrodden fields of anthropology: Observations on the esoteric Manners and Customs of Semi-civilized peoples, Being a record fo thirty Years Experience in Asia, Africa, America and Oceania, By a French Army Surgeon. Vol II, Paris 1898
The Italian surgeon, neurologist, physiologist and anthropologist, Paolo Mantegazza, also found a pattern of more potent negroes, specifically contradicting Tropinard who found negro advantage when flaccid. Mantegazza also references the work of another German scholar, who too, found negro length to be superior in any state. "Observations as to the shape and dimensions of the genital organs, in the various races, are not as yet very numerous; it is proved, however, that the Negroes generally have the virile member more voluminous than other people, and I myself verified this statement, during the years I practiced medicine n South America.. Falkenstein remarked that the Negroes of Loango had huge members and that their wives reproached our men with having such small yards. He rejects the singular idea of Topinard, who states that it is only when flabby that this enormous size is noticed.." --Gli Amori degli Uomini di Paolo Mantegazza, Senatore del Regno (Milan, 1892
White racist jealously of black potency has long historical roots scholars suggest, with white obsession so intense that black African penises where sometimes preserved and shipped to Europe as curiosities in colonial times.
"Some histories suggest that European explorers and slave traders sometines even perserved and pickled the penises of some African males, shipping the back to Europe as curiosities. Typically, the size of the African penis was held up as evidence of the "animalistic" and "subhuman" nature of the black race.
In 1954, in his analysis of the underpinnings of bias and racism, Gordon Allport referenced the preoccupation with sex and the black man's penis, suggesting that it was not the physical size of the penis, but the "psychological" size of the penis that was the fascination and preoccupation. In Calvin Hernton's work Sex and Race in America, Hernton describes the history of Southern white women's preoccupation with black men, suggesting that black males took on an iconic sexual persona." --David J. Ley. 2009. Insatiable wives
White envy and jealously may be related to cold climate evolution that led to smaller penises, some white writers argue
Summary by G. Howe, 1999
WHite biodiversity or heriditarian authors are much concerned about negro size, and conduct obsessive "self-assessment" to compare themselves with the more powerful blacks.. QUOTE:
"No criteria are ever set up to decide how these groups are established or what traits should be used in determin- ing membership. This means that his acceptance of "race" is ultimately arbitrary and subjective. When "the races" are compared in terms of appearance and performance in the quantities of uncritically collected data assembled in his book, "racial" identity is determined by "self-assessment." Rushton's basic units, then, are rooted in folk belief and not in biology.
The possibility that the vast majority of the human biological traits that have been shaped by evolution are clinally and independently distributed in association with the relevant selective forces is never once considered, and the word cline is simply missing. One running concern is how these folk categories compare on such matters as intelligence and reproductive behavior. Sex rears its head again and again in the discussion, with much of the information on comparative sexual performance based on "self- assessment." Rushton is obviously much taken with the "salience of... buttocks and breasts" (pp. 167, 231) as measures of sexuality, although there is a dearth of objectively collected data.
More telling is his evident fascination with the "Negroid" penis as an index of "potency" and libido. In his earlier publications on these matters, his information came from "self-assessment." --FROM: Review: Racialism and Racist Agendas Author(s): C. Loring Brace Reviewed work(s):Race, Evolution, and Behavior: A Life History Perspective by J. Philippe Rushton Source: American Anthropologist, New Series, Vol. 98, No. 1 (Mar., 1996), pp. 176-177
On numerous white racist websites, denizens of "the faithful" obsessively catalog interracial celebrity couples, with harsh racist rhetoric concealing hidden fears and jealously of black potency, as suggested by some white authors..
Feelings of inadequacy haunt white racists, directly and indirectly, among all white social classes, some white academic writers suggest..
"There is in the psyche of the racist an inordinate disposition for sexual atrocity. He sees in the Negro the essence of his own sexuality, that is. those qualities that he wishes for but fears he does not possess." --Hernton, Calvin 1965. Sex and Racism in America. Grove Press
"This was particularly salient to me when I gave a lecture on environmental racism before an audience of over 400 of North Carolina's "most gifted" high school seniors.. [who thought blacks lagged in some school academic areas] (except for athletic ability and — as many of my white students routinely point out — penis size).. --White college professor in American Philosophical Association newsletter, Spring 2004, vol 103, no 2
Envious southern whites also noted Negro potency, compared to whites, and in some incidents where blacks faced death for alleged crimes, the whites still noted the superior potency and continued virility of the doomed Negro. Dollard relates and incident where a negro sentenced to hang, requested a woman to spend with him, his last night on earth. "Hitting it" hard all night long, the negro duly "swung praying" in the morning. Unable to charge the official accounts to pay for the colored prostitute, the white lawmen could have simply dismissed her, but instead took up a collection to cover her costs, a sporting gesture in recognition of the vigorous negro's last ride. QUOTE:
"Seventeenth-century accounts of travel to West Africa included references to the "extraordinary greatness" of the "members" of the native males or of their large propagators..." Certainly [Mississippi] Delta white men discussed the matter of the length of the black man's penis with both anxiety and envy. One planter told Dollard of entering a sharecropper cabin unannounced and discovering a black man preparing for intercourse. Dollard's informant was shocked by the size of the man's penis 'and gave indication by his arm and clenched fist of its great length and diameter.' Local legend also had it that the belief in the greatness of the black mans penis was confirmed by those who conducted pre-induction physical examinations in the county in 1917" --James CObb. 1994. The Most Southern Place on Earth: The Mississippi Delta
and from Dollard 1998: "This virility-in-the-face-of-death is a good symbol of the potency of the Negro as it seems to the white man, and as it may indeed be in fact." --John Dollard, 1998. Caste and class in a southern town
Ancient Greeks and Romans noted black potency in their art
"The genitalia of black Africans were also deemed noteworthy to the Greek and Roman artists. Within the same art piece, black males are depicted with penises larger than those of white figures, and in others are shown as being erect." --Vincent Sarich, Frank Miele. 2005. Race: The Reality of Human Differences. pg 41
European explorers noted larger penises of Africans compared to whites "whereof these people are witnesse, who are furnis't with such members as are after a sort burthensome unto them.." European explorer Richard Jobson, 1632, observing the large penises of Mandingo tribesmen, in "The golden trade; or, A discovery of the river Gambra"
Likewise Muslim historian, al-Mas'udi, note of black Sudanese that they possessed: "elongated penises and excessive merriment". -- (see Akbar Muhammad, Slaves and Slavery in Muslim Africa, vol. I, p 68).
Racist architect of the Holocaust, Adolf Hitler's writings reveal an obsessive fear of negro sexual potency even when railing against Jews.. Quote:
"The myth of the over-sized black penis may be contrasted with the turn-of-the-century antisemitic belief that the large Jewish nose signified a small penis, further truncated by circumcision. Such images raised questions about Jewish masculinity and virility. But.. [the] notion of the Jew as cunning seducer, and occasionally a violent rapist, was a staple of Nazi propaganda. In his passage warning against 'the black-haired Jewish youth' Hitler also manages to arouse fears of lack sexuality when he blames Jews for the introduction into the Rhineland of soldiers from the French African colonies, some of who had affairs with German women that resulted in children of mixed ancestry.
Hitler even claimed that the French toleration of black-white intermarriage and its seeming color blind conception of assimilation was turning France into' an extension of Africa into the heartland of Europe'.. As for hundreds of mixed offspring sired on German women by French African colonial soldiers in the Rhineland during the early postwar years, they were rounded up and sterilized in 1937.." Had there been a significant black population in Germany, they might have conceivably have been sent to gas chambers along with all the Jews who could be apprehended and some of the Gypsies." ---George M. Fredrickson. 2003. Racism: A Short History. Princeton University Press. 120-121
Kinsey data confirmed by Kim...
Extensive Kinsey surveys report black dominance as well The Kinsey Data: Marginal Tabulations of the 1938-1963 Interviews Conducted by the Institute for Sex Research -- the 1979 follow-up to Alfred Kinsey's famous 1948 survey of male sexual practices in the United States - reported black advantage. From self-administered measurements given by roughly ten thousand whites and four hundred blacks, Kinsey Data authors Paul H. Gebhard and Alab B. Johnson found the average erect black penis to be longer in length (6.44 inches) and larger in circumference (4.96 inches) than corresponding white erections (6.15 and 4.83 respectively). Even larger differences occurred in the flaccid state. Blacks: 4.34 inches long, 3.78 around; whites 3.86 and 3.16)..
--Data from: Paul H. Gebhard and Alan B. Johnson, The Kinsey Data (Philadelphia: WB Saunders 1979), tables 69-73, pp 116-20)
Modern surveys report the same pattern
Reported by the British Medical Journal- "Penis Size By Ethnicity." - BMJ: British Medical Journal- Minerva: Volume 324, Issues 7336 2002
Other detailed studies note the same pattern of Negro dominance with inflated self-reporting especially prevalent among white gays. When measurements by a neutral observer are taken however, the Negro potency pattern still holds true across multiple studies.
Measured data 1 da ROs 1994, used neutral researchesr to measure erect penis lengths and did not rely on self-reporting which is often inflated. Their sample was 100% Caucasian. Average erect Caucasian length was 14.5 cm or 5.7 inches.[/b]
(SOURCE: da Ros, C., et al. 'Cauasian Penis: "What is the Normal SIze?" Journal of Urology, part 2, 151:323A (1994).
Measured data 2 - Other somewhat similar studies got averages of 5.35 inches and then 5.0", usually averaging below 6 inches. Wessells, Lue and McAninch 1996 also used a neutral researcher to measure erect men, and an involuntary drug induced erection technique- avoiding problems with inflated self-reporting. Their results were similar. With a mostly Caucasian sample, mean erect length was 12.8 cm or about 5 inches.
(SOURCE: Wessells, H., Lue, T. F., & McAninch, J. W. (1996). Penile length in the flaccid and erect states: Guidelines for penile augmentation. Journal of Urology, 156, 995–997.
QUOTE: "Wessells and McAninch conducted their size survey after several unhappy patients came to them with complications resulting from penile augmentation operations... By injecting 60 men with a drug that produces erections, and then measuring the size of their organs with a tape measure, Jack McAninch and Hunter Wessells of the University of California, San Francisco, concluded that an average erect penis is 12.8 centimeters long." --New Scientist, 2010. How to Make a Tornado: p151
Another study- confirms the same pattern of black potency. Surveys by condom makers also report the same
Another medical study conducted in the Philippines, and published in the International Journal of impotence research (2003) found that the average erect penile length was .. 12.9cm for occidentals [approx 5 inches].. Condom manufacturers Ansell, makers of Lifestyle condoms, who are keen to make condoms for all penis sizes in order to reduce condom failure, found that seventy-five percent of penises have an erect length of between 4.5 inches and 5.5 inches. In general, the average penis size of blacks is larger than of whites..[/i] --Source: International Journal of Impotence Research (2003) 15: 26-428
Debunking the myth of Italian men. The most comprehensive study of Italian men, over 3,000 army conscripts in the prime of life revealed small to moderate dimensions- an average of 12.5cm stretched length- about 5 inches. QUOTE:
The largest study on penile length was published in 2001 by Ponchietti et al.,  with a sample size of 3000 Italian men. The goal of their study was solely to determine the variability in penile size. Subjects ranged from age 17 to 19 years and measurements were recorded in the flaccid and flaccid stretched states. Flaccid circumference was recorded in the middle of the shaft. Mean flaccid length was 9.0 cm (s.d.=2.0), mean stretched length was 12.5 cm (s.d.= 2.5) and mean circumference was 10.0 cm (s.d.=0.75). --FROM: Ponchietti R et al. Penile length and circumference. A study on 3300 young Italian men. Eur Urol 2001; 39: 183-186. MEDLINE -- QUoted in: B.E. Dillon; N.B. Chama; S.C. Honig(2008) Int J Impot Res. 2008;20(5):519-529.
Posts: 5107 | From: The Hammer | Registered: Aug 2008
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