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Recent studies find the ancient Egyptians had a tropical body plan like sub-Saharan 'black' Africans and were not cold-adapted like European type populations. Tropical body plans also indicate darker-skin.

"The raw values in Table 6 suggest that Egyptians had the "super-Negroid" body plan described by Robins (1983).. This pattern is supported by Figure 7 (a plot of population mean femoral and tibial lengths; data from Ruff, 1994), which indicates that the Egyptians generally have tropical body plans. Of the Egyptian samples, only the Badarian and Early Dynastic period populations have shorter tibiae than predicted from femoral length. Despite these differences, all samples lie relatively clustered together as compared to the other populations." (Zakrzewski, S.R. (2003). "Variation in ancient Egyptian stature and body proportions". American Journal of Physical Anthropology 121 (3): 219-229.


a 2008 Study puts the ancient Egyptians closer to US Blacks than whites:

Quotes:

"Intralimb (crural and brachial) indices are significantly higher in ancient Egyptians than in American Whites (except crural index among females), i.e., Egyptians have relatively longer distal segments (Table 4). Intralimb indices are not significantly different between Egyptians and American Blacks... Many of those who have studied ancient Egyptians have commented on their characteristically ''tropical'' or ''African'' body plan (Warren, 1897; Masali, 1972; Robins, 1983; Robins and Shute, 1983, 1984, 1986; Zakrzewski, 2003). Egyptians also fall within the range of modern African populations (Ruff and Walker, 1993), but close to the upper limit of modern Europeans as well, at least for the crural index (brachial indices are definitely more ''African'').. In terms of femoral and tibial length to total skeletal height proportions, we found that ancient Egyptians are significantly different from US Blacks, although still closer to Blacks than to Whites.


Comparisons of linear body proportions of Old Kingdom and non-Old Kingdom period individuals, and workers and high officials in our sample found no statistically significant differences among them. Zakrzewski (2003) also found little evidence for differences in linear body proportions of Egyptians over a wider temporal range. In general, recent studies of skeletal variation among ancient Egyptians support scenarios of biological continuity through time. Irish (2006) analyzed quantitative and qualitative dental traits of 996 Egyptians from Neolithic through Roman periods, reporting the presence of a few outliers but concluding that the dental samples appear to be largely homogeneous and that the affinities observed indicate overall biological uniformity and continuity from Predynastic through Dynastic and Postdynastic periods.

Zakrzewski (2007) provided a comprehensive summary of previous Egyptian craniometric studies and examined Egyptian crania from six time periods. She found that the earlier samples were relatively more homogeneous in comparison to the later groups. However, overall results indicated genetic continuity over the Egyptian Predynastic and Early Dynastic periods, albeit with a high level of genetic diversity within the population, suggesting an indigenous process of state formation. She also concluded that while the biological patterning of the Egyptian population varied across time, no consistent temporal or spatial trends are apparent. Thus, the stature estimation formulae developed here may be broadly applicable to all ancient Egyptian populations.."
("Stature estimation in ancient Egyptians: A new technique based on anatomical reconstruction of stature." Michelle H. Raxter, Christopher B. Ruff, Ayman Azab, Moushira Erfan, Muhammad Soliman, Aly El-Sawaf, (Am J Phys Anthropol. 2008, Jun;136(2):147-55


Older limb studies find the same- Blacks and closer to the Egyptians than whites:

"In this regard it is interesting to note that limb proportions of Predynastic Naqada people in Upper Egypt are reported to be "Super-Negroid," meaning that the distal segments are elongated in the fashion of tropical Africans.....skin color intensification and distal limb elongation are apparent wherever people have been long-term residents of the tropics." (C.L. Brace, 1993. Clines and clusters..")


"An attempt has been made to estimate male and female Egyptian stature from long bone length using Trotter & Gleser negro stature formulae, previous work by the authors having shown that these rather than white formulae give more consistent results with male dynastic material... When consistency has been achieved in this way, predynastic proportions are founded to be such that distal segments of the limbs are even longer in relation to the proximal segments than they are in modern negroes. Such proportions are termed "super-negroid"...

Robins (1983) and Robins & Shute (1983) have shown that more consistent results are obtained from ancient Egyptian male skeletons if Trotter & Gleser formulae for negro are used, rather than those for whites which have always been applied in the past. .. their physical proportions were more like modern negroes than those of modern whites, with limbs that were relatively long compared with the trunk, and distal segments that were long compared with the proximal segments. If ancient Egyptian males had what may be termed negroid proportions, it seems reasonable that females did likewise."
(Robins G, Shute CCD. 1986. Predynastic Egyptian stature and physical proportions. Hum Evol 1:313-324. Ruff CB. 1994.)





The ancient Badarians were quite representative of ancient Egyptians as a whole and showed clear links with tropical Africans to the south. They have been sometimes excluded in studies of the ancient Egyptian population, which shows continuity in its history, not mass influxes of foreigners until the late periods.

Quotes:
"As a result of their facial prognathism, the Badarian sample has been described as forming a morphological cluster with Nubian, Tigrean, and other southern (or \Negroid") groups (Morant, 1935, 1937; Mukherjee et al., 1955; Nutter, 1958, Strouhal, 1971; Angel, 1972; Keita, 1990). Cranial nonmetric trait studies have found this group to be similar to other Egyptians, including much later material (Berry and Berry, 1967, 1972), but also to be significantly different from LPD material (Berry et al., 1967). Similarly, the study of dental nonmetric traits has suggested that the Badarian population is at the centroid of Egyptian dental samples (Irish, 2006), thereby suggesting similarity and hence continuity across Egyptian time periods. From the central location of the Badarian samples in Figure 2, the current study finds the Badarian to be relatively morphologically close to the centroid of all the Egyptian samples. The Badarian have been shown to exhibit
greatest morphological similarity with the temporally successive EPD (Table 5). Finally, the biological distinctiveness
of the Badarian from other Egyptian samples has also been demonstrated (Tables 6 and 7).

These results suggest that the EDyn do form a distinct morphological pattern. Their overlap with other Egyptian samples (in PC space, Fig. 2) suggests that although their morphology is distinctive, the pattern does overlap with the other time periods. These results therefore do not support the Petrie concept of a \Dynastic race" (Petrie, 1939; Derry, 1956). Instead, the results suggest that the Egyptian state was not the product of mass movement of populations into the Egyptian Nile region, but rather that it was the result of primarily indigenous development combined with prolonged small-scale migration, potentially from trade, military, or other contacts.

This evidence suggests that the process of state formation itself may have been mainly an indigenous process, but that it may have occurred in association with in-migration to the Abydos region of the Nile Valley. This potential in-migration may have occurred particularly during the EDyn and OK. A possible explanation is that the Egyptian state formed through increasing control of trade and raw materials, or due to military actions, potentially associated with the use of the Nile Valley as a corridor for prolonged small scale movements through the desert environment.
(Sonia R. Zakrzewski. (2007). Population Continuity or Population Change: Formation of the Ancient Egyptian State. AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 132:501-509)






Ancient Egyptians most related to other Africans and are part of a Nilotic continuity rather than something Mediterranean or Middle Eastern

"Certainly there was some foreign admixture [in Egypt], but basically a homogeneous African population had lived in the Nile Valley from ancient to modern times... [the] Badarian people, who developed the earliest Predynastic Egyptian culture, already exhibited the mix of North African and Sub-Saharan physical traits that have typified Egyptians ever since (Hassan 1985; Yurco 1989; Trigger 1978; Keita 1990.. et al.,)... The peoples of Egypt, the Sudan, and much of East African Ethiopia and Somalia are now generally regarded as a Nilotic continuity, with widely ranging physical features (complexions light to dark, various hair and craniofacial types) but with powerful common cultural traits, including cattle pastoralist traditions.." (Frank Yurco, "An Egyptological Review," 1996 -in Mary R. Lefkowitz and Guy MacLean Rogers, Black Athena Revisited, 1996, The University of North Carolina Press, p. 62-100)
African peoples are the most diverse in the world whether analyzed by DNA or skeletal or cranial methods. Attempts to deny this are rooted in racism and error. African people, particularly SUB-SAHARAN Africans, vary the most in how they look, more so than any other population in the world.

"Estimates of genetic diversity in major geographic regions are frequently made by pooling all individuals into regional aggregates. This method can potentially bias results if there are differences in population substructure within regions, since increased variation among local populations could inflate regional diversity. A preferred method of estimating regional diversity is to compute the mean diversity within local populations. Both methods are applied to a global sample of craniometric data consisting of 57 measurements taken on 1734 crania from 18 local populations in six geographic regions: sub-Saharan Africa, Europe, East Asia, Australasia, Polynesia, and the Americas. Each region is represented by three local populations.

Both methods for estimating regional diversity show sub-Saharan Africa to have the highest levels of phenotypic variation, consistent with many genetic studies."
(Relethford, John "Global Analysis of Regional Differences in Craniometric Diversity and Population Substructure". Human Biology - Volume 73, Number 5, October 2001, pp. 629-636)

"The living peoples of the African continent are diverse in facial characteristics, stature, skin color, hair form, genetics, and other characteristics. No one set of characteristics is more African than another. Variability is also found in "sub-Saharan" Africa, to which the word "Africa" is sometimes erroneously restricted. There is a problem with definitions. Sometimes Africa is defined using cultural factors, like language, that exclude developments that clearly arose in Africa. For example, sometimes even the Horn of Africa (Somalia, Ethiopia, Eritrea) is excluded because of geography and language and the fact that some of its peoples have narrow noses and faces.

However, the Horn is at the same latitude as Nigeria, and its languages are African. The latitude of 15 degree passes through Timbuktu, surely in "sub-Saharan Africa," as well as Khartoum in Sudan; both are north of the Horn. Another false idea is that supra-Saharan and Saharan Africa were peopled after the emergence of "Europeans" or Near Easterners by populations coming from outside Africa. Hence, the ancient Egyptians in some writings have been de-Africanized. These ideas, which limit the definition of Africa and Africans, are rooted in racism and earlier, erroneous "scientific" approaches." (S. Keita, "The Diversity of Indigenous Africans," in Egypt in Africa, Theodore Clenko, Editor (1996), pp. 104-105. [10])






Modern DNA studies find even though some African peoples look different, they are genetically related through the PN2 transition clade of the Y-chromosone. Thus light-skinned African Libyans and dark-skinned Zulus are all genetically related Africans ,even though they don't look exactly the same.

"But the Y-chromosome clade defined by the PN2 transition (PN2/M35, PN2/M2) shatters the boundaries of phenotypically defined races and true breeding populations across a great geographical expanse. African peoples with a range of skin colors, hair forms and physiognomies have substantial percentages of males whose Y chromosomes form closely related clades with each other, but not with others who are phenotypically similar. The individuals in the morphologically or geographically defined 'races' are not characterized by 'private' distinct lineages restricted to each of them." (S O Y Keita, R A Kittles, et al. "Conceptualizing human variation," Nature Genetics 36, S17 - S20 (2004)


"Recall that the Horn-Nile Valley crania show, as a group, the largest overlap with other regions. A review of the recent literature indicates that there are male lineage ties between African peoples who have been traditionally labeled as being ''racially'' different, with ''racially'' implying an ontologically deep divide. The PN2 transition, a Y chromosome marker, defines a lineage (within the YAPþ derived haplogroup E or III) that emerged in Africa probably before the last glacial maximum, but after the migration of modern humans from Africa (see Semino et al., 2004). This mutation forms a clade that has two daughter subclades (defined by the biallelic markers M35/215 (or 215/M35) and M2) that unites numerous phenotypically variant African populations from the supra-Saharan, Saharan, and sub-Saharan regions.."
(S.O.Y Keita. Exploring northeast African metric craniofacial variation at the individual level: A comparative study using principal component analysis. Am. J. Hum. Biol. 16:679-689, 2004.)
keita2004neanalysis.htm

"Africa contains tremendous cultural, linguistic and genetic diversity, and has more than 2,000 distinct ethnic groups and languages.. Studies using mitochondrial (mt)DNA and nuclear DNA markers consistently indicate that Africa is the most genetically diverse region of the world." (Tishkoff SA, Williams SM., Genetic analysis of African populations: human evolution and complex disease. Nature Reviews Genetics. 2002 Aug (8):611-21.)

DNA of some modern Egyptians found a genetic ancestral heritage to East Africa:
"The mitochondrial DNA (mtDNA) diversity of 58 individuals from Upper Egypt, more than half (34 individuals) from Gurna, whose population has an ancient cultural history, were studied by sequencing the control-region and screening diagnostic RFLP markers. This sedentary population presented similarities to the Ethiopian population by the L1 and L2 macrohaplogroup frequency (20.6%), by the West Eurasian component (defined by haplogroups H to K and T to X) and particularly by a high frequency (17.6%) of haplogroup M1. We statistically and phylogenetically analysed and compared the Gurna population with other Egyptian, Near East and sub-Saharan Africa populations; AMOVA and Minimum Spanning Network analysis showed that the Gurna population was not isolated from neighbouring populations. Our results suggest that the Gurna population has conserved the trace of an ancestral genetic structure from an ancestral East African population, characterized by a high M1 haplogroup frequency. The current structure of the Egyptian population may be the result of further influence of neighbouring populations on this ancestral population."
(Stevanovitch A, Gilles A, Bouzaid E, et al. (2004) Mitochondrial DNA sequence diversity in a sedentary population from Egypt.Ann Hum Genet. 68(Pt 1):23-39.)

Tishkoff et al:

"Africa contains tremendous cultural, linguistic and genetic diversity, and has more than 2,000 distinct ethnic groups and languages (see online link to Ethnologue). Studies using mitochondrial (mt)DNA and nuclear DNA markers consistently indicate that Africa is the most genetically diverse region of the world(TABLE 1).However,most studies report only a few markers in divergent African populations, which makes it difficult to draw general conclusions about the levels and patterns of genetic diversity in these populations (FIG. 1). Because genetic studies have been biased towards more economically developed African countries that have key research or medical centres, populations from more underdeveloped or politically unstable regions of Africa remain undersampled (FIG. 1). Historically, human population genetic studies have relied on one or two African populations as being representative of African diversity, but recent studies show extensive genetic variation among even geographically close African populations, which indicates that there is not a single 'representative' African population."
-- Tishkoff NATURE REVIEWS | GENETICS VOLUME 3 | AUGUST 2002


"Genetic studies that attempt to recover the biological history of the species have generally found that there is a split between their restricted African samples and "the rest of the world." These approaches conceptualize human population history as a series of bifurcations with each node being relatively uniform. The "Africans" usually used are either the short statured Aka or Mbuti, Khoisan speakers, or West African stereotype s, in keeping with a socially, not scientifically constructed concept of African. Studies using individuals as the unit of analysis evince a different pattern. A select subset of Africans called the "group of 49" forms a unit versus the rest of humankind. However the latter individuals ("rest of humankind") also includes non-East African sub-Saharans. Hence there is no "racial" split. As has been stated, the idea that human variation can be described as being structured by subspecies(races) that are treated as lineages is fundamentally false. In actuality, also, although averages are used, the gene studies usually give us histories that are not necessarily the same as population histories."
Writing African History Chapter 4, Physical Anthropology and African History, Shomarka Keita University of Rochester Press p.134

Continent wide African DNA linkages
"The most extensive pan-African haplotype (16189 16192 16223 16278 16294 16309 16390) is in the L2a1 haplogroup. This sequence is observed in West Africa among the Malinke, Wolof, and others; in North Africa among the Maure, Hausa, Fulbe, and others; in Central Africa among the Bamileke, Fali, and others; in South Africa among the Khoisan family including the Khwe and Bantu speakers; and in East Africa among the Kikuyu. Closely related variants are observed among the Tuareg in North and West Africa and among the East African Dinka and Somali."
(-- Bert Ely , Jamie Lee Wilson , Fatimah Jackson and Bruce A Jackson. (2006). African-American mitochondrial DNAs often match mtDNAs found in multiple African ethnic groups. BMC Biology 2006, 4:34)

"It is of interest that the M35 and M2 lineages are united by a mutation - the PN2 transition. This PN2 defined clade originated in East Africa, where various populations have a notable frequency of its underived state. This would suggest that an ancient population in East Africa, or more correctly its males, form the basis of the ancestors of all African upper Paleolithic populations - and their subsequent descendants in the present day."
(--Bengtson, John D. (ed.), In Hot Pursuit of Language in Prehistory: Essays in the four fields of anthropology. 2008. John Benjamins Publishing: pp. 3-16)



Egyptian Y-chromosome haplotypes show preponderance is with African clusters not Europe or the Near East


Other DNA quotes from S.O.Y. Keita
See: http://www.geocities.com/keitadnaquotes.htm


Recent DNA studies of the Sudan show genetic unity and linkage between the Sudanic, Horn, Egyptian, Nubian and other Nilotic peoples, confirming earlier skeletal/cranial studies and historical data. (Yurco (1989, 1996), Keita (1993,2004, 2005) Lovell (1999), Zakrewski (2003, 2007) et. al). Of note is that DNA data shows that some peoples linked to one of the oldest Egyptian populations, the original Copts, have a significant frequency of the B-M60 marker, indicating early colonization of Egypt by Nilotics in the state formation period.

QUOTES:

"Haplogroup E-M78, however, is more widely distributed and is thought to have an origin in eastern African. More recently, this haplogroup has been carefully dissected and was found to depict several well-established subclades with defined geographical clustering (Cruciani et al., 2006, 2007). Although this haplogroup is common to most Sudanese populations, it has exceptionally high frequency among populations like those of western Sudan (particularly Darfur) and the Beja in eastern Sudan... Although the PC plot places the Beja and Amhara from Ethiopia in one sub-cluster based on shared frequencies of the haplogroup J1, the distribution of M78 subclades (Table 2) indicates that the Beja are perhaps related as well to the Oromo on the basis of the considerable frequencies of E-V32 among Oromo in comparison to Amhara (Cruciani et al., 2007)...

These findings affirm the historical contact between Ethiopia and eastern Sudan (1998), and the fact that these populations speak languages of the Afroasiatic family tree reinforces the strong correlation between linguistic and genetic diversity (Cavalli-Sforza, 1997)."

"Genetic continuum of the Nubians with their kin in southern Egypt is indicated by comparable frequencies of E-V12 the predominant M78 subclade among southern Egyptians."

"The Copt samples displayed a most interesting Y-profile, enough (as much as that of Gaalien in Sudan) to suggest that they actually represent a living record of the peopling of Egypt. The significant frequency of B-M60 in this group might be a relic of a history of colonization of southern Egypt probably by Nilotics in the early state formation, something that conforms both to recorded history and to Egyptian mythology."
Source:
(Hisham Y. Hassan 1, Peter A. Underhill 2, Luca L. Cavalli-Sforza 2, Muntaser E. Ibrahim 1. (2008). Y-chromosome variation among Sudanese: Restricted gene flow, concordance with language, geography, and history. Am J Phys Anthropology, 2008.)


Older research notes the physical makeup of the original Copts, now confirmed by recent DNA data above:
"In Libya, which is mostly desert and oasis, there is a visible Negroid element in the sedentary populations, and at the same is true of the Fellahin of Egypt, whether Copt or Muslim. Osteological studies have shown that the Negroid element was stronger in predynastic times than at present, reflecting an early movement northward along the banks of the Nile, which were then heavily forested." (Encyclopedia Britannica 1984 ed. "Populations, Human")


Haplogroup E3A and E3B represent more than 70% of the Y-chromosones on the African continent, with varying proportions found in different parts of the continent. In some African populations for example, E3B exceeds 80%. Migrations out of Africa, are responsible for the spread of E3b to Europe. Non-Africans thus acquired a sub-set f African genes through this migration.


"In Europe, the overall frequency pattern of haplogroup E-M78 does not support the hypothesis of a uniform spread of people from a single parental Near Eastern population... The Y chromosome specific biallelic marker DYS271 defines the most common haplogroup (E3a) currently found in sub-Saharan Africa. A sister clade, E3b (E-M215), is rare in sub-Saharan Africa, but very common in northern and eastern Africa. On the whole, these two clades represent more than 70% of the Y chromosomes of the African continent. A third clade belonging to E3 (E3c or E-M329) has been recently reported to be present only in eastern Africa, at low frequencies.. The new topology of the E3 haplogroup is suggestive of a relatively recent eastern African origin for the majority of the chromosomes presently found in sub-Saharan Africa."

"In conclusion, we detected the signatures of several distinct processes of migration and/or recurrent gene flow associated with the dispersal of haplogroup E3b lineages. Early events involved the dispersal of E-M78d chromosomes from eastern Africa into and out of Africa, as well as the introduction of the E-M34 subclade into Africa from the Near East. Later events involved short-range migrations within Africa (E-M78? and E-V6) and from northern Africa into Europe (E-M81 and E-M78ß), as well as an important range expansion from the Balkans to western and southern-central Europe (E-M78a). This latter expansion was the main contributor to the present distribution of E3b chromosomes in Europe."

(Cruciani, F, et. al. (2004) Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa, Am J Hum Genet. 74(5): 1014-1022.)


Somalis link much more heavily with African populations such as those in Kenya and Ethiopia than Middle Eastern or European ones according to DNA evidence. Eurasian genes only accounted for about 15% of the mix among Somalis, typically associated with recent Arab influence. On such key common DNA markers as E3b1, Europeans only weighed in at 5%, and Middle Easterners at approximately 6%. The overwhelming link of Somalis- over 85% of the total is with Africans. Kenya and Ethiopia are located in "sub-Saharan" Africa.

"The high frequency (77.6%) of haplogroup E3b1 was characteristic of male Somalis. The frequency of E3b1 was significantly lower in Ethiopian Oromos (35.9%), Ethiopian Amharas (22.9%), Egyptians (20.0%), Sudanese (17.5%), Kenyans (15.1%),10 Iraqis (6.3%), Northern Africans (6.1%), Southern Europeans (0.5-5.1%) and sub-Saharan populations." (Sanchez et al.,(2005) High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males, Eu J of Hum Genet (2005) 13, 856-866)

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Posts: 26260 | From: Atlanta, Georgia, USA | Registered: Feb 2005  |  IP: Logged | 

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Originally posted by Djehuti:
^ The problem is that Takruri, Evergreen and others cite scholarly evidence everyday while YOU cite non!

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Posts: 4165 | From: jamaica | Registered: May 2008  |  IP: Logged | 

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Originally posted by ausar:
Some people need to reaize that a certain subsection of our population are sociopaths. Sociopaths enjoy playing mind games with people. Since they lack an outlet in the real world they attempt to use Egyptsearch as their personal playground. It's that simple.

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Posts: 2595 | From: Vicksburg | Registered: Feb 2006  |  IP: Logged | 

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Originally posted by Djehuti:
^ Looks to me like the opposite-- the more we feed him with TRUTH the smaller and weaker he gets which is why he not only stopped responding but also stopped creating new threads.

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Posts: 4021 | From: Bay Area, CA | Registered: Mar 2007  |  IP: Logged | 

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You appear to have been exposed

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Posts: 4165 | From: jamaica | Registered: May 2008  |  IP: Logged | 

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Originally posted by Sundjata:
... The guy has been creating more threads the more you and others engage him. I'm simply pleading with you and the like to stop looking weak with this incessant back and fourth garbage, bickering and foul language.

Surely bickering with trolls constantly on a forum does nothing but annoy most members there, but I realize some people just don't give a sh1t if their actions are helping to run people away.

... I'm done trying to salvage any thing left of the spirit once pervasive here.

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Posts: 8014 | From: the Tekrur in the Western Sahel | Registered: Feb 2006  |  IP: Logged | 

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Originally posted by Brada-Anansi:
@ T-REX,there was no need to slam Mongolians especially since dirk8 is not even one, but a confused racist attention seeking afarengi troll, who uses multiple alias,sometimes Glider,sometimes Abaza and so on,everyone should stay clear of him as he is a Master.......Baiter!!!

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Posts: 7081 | From: Fallbrook, CA | Registered: Mar 2004  |  IP: Logged | 

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Originally posted by BrandonP:

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Originally posted by Brada-Anansi:
@ T-REX,there was no need to slam Mongolians especially since dirk8 is not even one, but a confused racist attention seeking afarengi troll, who uses multiple alias,sometimes Glider,sometimes Abaza and so on,everyone should stay clear of him as he is a Master.......Baiter!!!

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I was doing that to parody of Dirk8's anti-African tactics. Truthfully, I have nothing against Mongolians. In fact, I will admit that for all their cruelty, the Mongols did unify most of Eurasia into a coherent polity and facilitate trade between East and West, therefore allowing the civilizations of Asia to influence European development.

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Posts: 527 | From: usa | Registered: Apr 2009  |  IP: Logged | 

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Originally posted by Simple Girl:

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Originally posted by BrandonP:

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Originally posted by Brada-Anansi:
@ T-REX,there was no need to slam Mongolians especially since dirk8 is not even one, but a confused racist attention seeking afarengi troll, who uses multiple alias,sometimes Glider,sometimes Abaza and so on,everyone should stay clear of him as he is a Master.......Baiter!!!

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I was doing that to parody of Dirk8's anti-African tactics. Truthfully, I have nothing against Mongolians. In fact, I will admit that for all their cruelty, the Mongols did unify most of Eurasia into a coherent polity and facilitate trade between East and West, therefore allowing the civilizations of Asia to influence European development.

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Oh is this really the case? Can you provide the evidence for this? Why then has European innovations dwarfed Asian achievements even though Asians have greatly outnumbered Europeans? Can you show me where Asians have paralled or at some point exceeded the achievements of Europeans at any or all levels?

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Posts: 7081 | From: Fallbrook, CA | Registered: Mar 2004  |  IP: Logged |