- Maghrebis
-
Maghrebian People
مغاربه - M'ɣarba
ⵎⴰⴳⵕⵉⴱⵉTotal population ~98 Millions Regions with significant populations North Africa 87,979,238 Algeria 34,994,937 Morocco 31,968,361 [1] Tunisia 10,629,186 ~10 Millions [2][3][4] Libya 6,597,960 Mauritania 3,281,634 Western Sahara 507,160 Languages official: Arabic • Berber
Religion Mostly Muslims
Christianity, Atheism, JudaismRelated ethnic groups Mediterranean race • Arabs
Footnotes Population statistics from the world factbook (July 2011 pop est.) Maghrebis or Maghrebian people or Maghrebians are the inhabitants of the Maghreb countries (Morocco, Algeria, Tunisia, Libya, Mauritania).
Contents
Origins
The inhabitants of the region are predominantly "Arab-Berbers" but this term implies a complete fusion of the two groups which is not the case. Whereas Arabs and Berbers, united through Islam are the main ethnic and cultural elements, it is important to bear in mind that over the centuries the Maghreb has been a melting-pot of many other ethnic groups and cultures. Before the Arab conquest Phoenicians, Greeks, Romans, Vandals, and Byzantines colonized the Maghreb and contributed to the development of its culture. Later, moriscos and muladies, that is, indigenous Spaniards who had earlier converted to the Muslim faith and were fleeing, together with ethnic Arab and Berber Muslims, from the Catholic Reconquista settled to the Maghreb. Among West Asians are Turks who came over with the expansion of the Ottoman Empire. A small Turkish descended population exists, particularly in Tunisia and Algeria. Other European contributions included French, Italians, and others captured by the corsairs and then turned into slaves.[5]
Nowadays, a majority of the current population in the Maghreb consider themselves generally Arab in identity, regardless of mixed ethnic or linguistic heritage. There are significant non-Arab or non-Arab identifying populations in the region and most important of the non-Arab populations found throughout the Maghreb, particularly in Morocco and Algeria, are the Berbers. They represented the majority of the pre-Islamic population. After the arrival of Islamic Arabs, Berbers assimilated in large numbers to Arab or mixed Arab-Berber ethnic identities.
Historically the Maghreb was also home to significant Jewish communities, including the Maghrebim Jews, who predated the 7th century introduction and conversion of the majority of Berbers to Islam. Under the Almohad dynasty rule in the 12th century, the Jews were forced to convert en masse to Islam.[6] Later largely augmented by Spanish Sephardi Jews, fleeing the Spanish Catholic Reconquista, established a presence in North Africa, chiefly in the urban trading centers. They have contributed to the wider population through conversion and assimilation. Many Sephardic Jews emigrated to North America in the early 20th century or to France and Israel later in the 20th century.
On the Saharan southern edge of the Maghreb are large communities of black populations, sometimes called Haratin, who are orally identify themselves as the original inhabitants of southern oasis.
Religion
Historic records of religion in the Maghreb region show its gradual inclusion in the Classical World, with coastal colonies established first by Phoenicians, some Greeks, and later extensive conquest and colonization by the Romans. By the 2nd century common era, the area had become a center of Latin-speaking Christianity. Both Roman settlers and Romanized populations converted to Christianity. The region produced figures such as Christian Church writer Tertullian (c. 155 – c. 202); and Christian Church martyrs or leading figures such as St Cyprian of Carthage (+ 258); Saint Monica; her son the philosopher St. Augustine, Bishop of Hippo I (+ 430) (1); and St Julia of Carthage (5th century).
The domination of Christianity ended when Arab invasions brought Islam in 647. Carthage fell in 698 and the remainder of the region followed in subsequent decades. Gradual Islamization proceeded, although surviving letters showed correspondence from regional Christians to Rome up until the 9th century. Christianity was still a living faith. Christian bishoprics and dioceses continued to be active, with relations continuing with Rome. As late as Pope Benedict VII (974-983) reign, a new Archbishop of Carthage was consecrated. Evidence of Christianity in the region then faded through the 10th century.
During the 7th century, the region's peoples began their nearly total conversion to Islam. There is a small but thriving Jewish community, as well as a small Christian community. Most Muslims follow the Sunni Maliki school. Small Ibadi communities remain in some areas. A strong tradition of venerating marabouts and saints' tombs is found throughout regions inhabited by Berbers. Any map of the region demonstrates the tradition by the proliferation of "Sidi"s, showing places named after the marabouts. Like some other religious traditions, this has substantially decreased over the 20th century. A network of zaouias traditionally helped proliferate basic literacy and knowledge of Islam in rural regions.
Culture
Diaspora
France
According to Michel Tribalat, a researcher at INED, there were 3.5 million people of Maghrebi origin (with at least one grandparent from Algeria, Morocco or Tunisia) living in France in 2005 corresponding to 5.8% of the total French metropolitan population (60.7 millions in 2005).[7] Maghrebis have settled mainly in the industrial regions in France, especially in the Paris region. Many famous French people like Edith Piaf[8], Isabelle Adjani, Arnaud Montebourg, Alain Bashung, Dany Boon and many others have Maghrebi ancestry.
Below is a table of population of Maghrebi origin in France, numbers are in thousands:
Country 1999 2005 % 1999/2005 % French population (60.7 millions in 2005) Algeria 1,577 1,865 +18.3% 3.1% Immigrants 574 679 Born in France 1,003 1,186 Morocco 1,005 1,201 +19.5% 2.0% Immigrants 523 625 Born in France 482 576 Tunisia 417 458 +9.8% 0.8% Immigrants 202 222 Born in France 215 236 Total Maghreb 2,999 3,524 +17.5% 5.8% Immigrants 1 299 1 526 2.5% Born in France 1 700 1 998 3.3% In 2005, the percentage of young people under 18 of maghrebi origin (at least one immigrant parent) was about 7% in Metropolitan France, 12% in Greater Paris and above 20% in French département of Seine-Saint-Denis.[9][10]
2005 % Seine-Saint-Denis Val-de-Marne Val-d'Oise Lyon Paris France Total Maghreb 22.0% 13.2% 13.0% 13.0% 12.1% 6.9% According to other sources between 5 and 8 million people of Maghrebin origin live in France.[11][12]
Anthropology, Genetics and Linguistics
Various disciplines shed light on the origin of the Northwest-Africans (Berbers and Arabs).
Physical anthropology
Northwest-Africans are defined as Mediterraneans with moderate Alpinid and Nordic elements.[13] A significant proportion of the Rif Berbers, Kabyles and Chouias have blue or green eyes, a percentage sometimes higher than that found in Sicilians or Spaniards.[14]
Genetic evidence
The genetic proximity observed between the Northwest-Africans and Southern Europeans is due to the fact that both these groups shared a common ancestor either in the Upper Paleolithic, in the Neolithic or alternatively during history with the invasion and the occupation during nearly seven centuries of the Iberian Peninsula by Moorish troops.[15]
Y-chromosome DNA
The Y-chromosome genetic structure of the Maghreb population seems to be mainly Modulated by geography, The Y-DNA Haplogroups E3b and J, which are so common among the population of North African and the Middle East, Haplogroups E3b and J, are the most widespread among North African groups especially E1b1b1b (E-M81, formerly E3b1b) which is typical of the indigenous Berbers of North-West Africa. In some parts of Morocco E1b1b1b can peak at 80% of the population. Followed by Haplogroup J especially J1[16] [1] , which is typically Middle Eastern which can reach frequencies of 35% in the region,[17][18] and has its highest density founded in the Southwestern Arabian Peninsula,[18] Followed by Haplogroup R1[19] which has been observed in North African though with lower frequency. The Y-DNA Haplogroups shown above are observed in both Arab and Berber-speakers.
The Northwest-African Y chromosome pool (including both Berber and Arab populations) may be summarized as follows where only two haplogroups E1b1b and J comprise generally more than 80% of the total chromosomes:[20][21][22][23][24][25][26]
- E1b1b (mainly E-M81) (50-100 %)
- J (mainly J1-M267) (0-45%)
- R1b (0-15%)
- Sub-Saharan and other haplogroups (0-8%)
E1b1b1b (E-M81) is the most common Y haplogroup among North African Arabs and Berbers dominated by its sub-clade E-M183. It is thought to have originated in North Africa 5,600 years ago.[23][24] Colloquially referred to as the "Berber marker" for its prevalence among Mozabite, Middle Atlas, Kabyle and other Berber groups, E-M81 is also quite common among North African Arab groups (45% in Oran).[25] It can reach frequencies of up to 80% in the Maghreb.
Regarding J1-M267, according to a recent study in 2011 about Tunisia, it is significantly more abundant in the urban (31.3%) than in the rural total population (2.5%). According to the authors, these results could be explained supposing that Arabization in Tunisia was a military enterprise, therefore, mainly driven by men that displaced native Berbers to geographically marginal areas but that frequently married Berber women.[27]
Population Nb A/B E(xE1b1b1) E1b1b1 E1b1b1a E1b1b1b E1b1b1c F K G I J1 J2 R1a R1b-M269 Other Study 1 Algeria/Oran 102 0 7.9% 0 5.9% 45.1% 0 0 0 0 0 22.5% 4.9% 1% 11.8% 1% Robino et al. (2008)[28] 2 Algeria/Algiers 35 0 2.9% 0 11.4% 42.9% 0 11.8% 2.9% 0 0 22.9% 5.7% 0 0 0 Arredi et al. (2004)[29] 3 Algeria/Tizi Ouzou 19 0 0 0 0 47.4% 10.5% 10.5% 0 0 0 15.8% 0 0 15.8% 0 Arredi et al. (2004) 4 Tunisia/Tunis 148 0 2% 3.4% 5.4% 37.8% 2.7% 4.7% 0.7% 0 0 32.4% 3.4% 0.7% 6.1% 0.7% Arredi et al. (2004) 5 Tunisia 52 0 0 9.6% 15.4% 32.7% 0 1.9% 1.9% 0 0 34.6% 3.8% 0 0 0 Onofri et al. (2008) 6 Tunisia/Bou Omrane 40 0 5% 0 5% 87.5% 0 2.5% 0 0 0 0 0 0 0 0 Ennafaa et al. (2011)[30] 7 Tunisia/Bou Saad 40 0 0 0 0 92.5% 0 0 0 0 0 5% 0 0 0 2.5% Ennafaa et al. (2011) 8 Tunisia/Jerbian Arabs 46 2.2% 0 0 15.2% 60.9% 4.3% 0 0 0 0 8.7% 2.2% 4.3% 2.2% 0 Ennafaa et al. (2011) 9 Tunisia/Jerbian Berbers 47 0 0 0 17% 76.6% 0 4.25% 2.1% 0 0 0 0 0 0 0 Ennafaa et al. (2011) 10 Tunisia/Chenini–Douiret Berbers 27 0 0 0 0 100% 0 0 0 0 0 0 0 0 0 0 Karima Fadhlaoui-Zid et al. (2011)[31] 11 Tunisia/Sened Berbers 35 0 0 0 0 65.7% 0 2.9% 0 0 0 31.4% 0 0 0 0 Karima Fadhlaoui-Zid et al. (2011) 12 Tunisia/Jradou Berbers 32 0 0 0 0 100% 0 0 0 0 0 0 0 0 0 0 Karima Fadhlaoui-Zid et al. (2011) 13 Tunisia/Andalusian Zaghouan 32 0 0 0 3.1% 40.6%% 0 9.4% 0 0 0 43.8% 3.1% 0 0 0 Karima Fadhlaoui-Zid et al. (2011) 14 Tunisia/Cosmopolitan Tunis 33 0 0 3.0% 6.0% 54.5%% 3.0% 6.0% 0 3.0% 0 24.2% 0 0 0 0 Karima Fadhlaoui-Zid et al. (2011) 15 Morocco 221 0 6.4% 4.1% 6.8% 65% 0 0.9% 1.8% 0.9% 0.5% 5% 4.1% 0 4.1% 0 Fregel et al. (2009) 16 Morocco 51 3.9% 5.9% 5.9% 5.9% 54.9% 0 0 0 0 0 19.60% 0 0 3.9% 0 Onofri et al. (2008) 17 Morocco/Amizmiz Valley 33 3% 6.1% 0 3% 84.8% 3% 0 0 0 0 0 0 0 0 0 Alvarez et al. (2009) 18 Sahrawi 89 0 20.2% 0 0 59.6% 0 0 0 0 0 20.2% 0 0 0 0 Fregel et al. (2009) Mitochondrial DNA
Many studies[32][33][34][35][36][37][38][39][40][41][42][43][44] have attempted to describe the genetic diversity of Northwest-African populations, evaluating mitochondrial DNA (mtDNA) sequence variation and the results may be summarized as follows (data for 536 individuals from 9 populations : Morocco (Asni, Bouhria, Figuig, Souss), Algeria (Mozabites), Tunisia (Chenini-Douiret, Sened, Matmata, Jerba)[15]):
- Total Eurasian lineages (H, HV0, HV, R0, J, T, U (without U6), K, N1, N2, X) : 50-90% with an average of about 5/8
- Total sub-Saharan lineages (L0, L1, L2, L3, L4-L5) : 3-50% with an average of about 2/8
- Total North African lineages (U6, M1) : 0-35% with an average of about 1/8
The Northwest-African mtDna pool is characterized by an "overall high frequency of Western Eurasian haplogroups, a somehow lower frequency of sub-Saharan L lineages, and a significant (but differential) presence of North African haplogroups U6 and M1."[15] According to Cherni et al. 2009 "the post-Last glacial maximum expansion originating in Iberia not only led to the resettlement of Europe but also of North Africa".[44]
According to a Ottoni et al. 2010, besides the "autochthonous" South-Saharan component, the maternal pool of Northern Africa appears to be characterized by at least two other major components: (i) a Levantine contribution (i.e. haplogroups U6 and M1), associated with the return to Africa around 45 kya, and (ii) a more recent West European input associated with the postglacial expansion.[45]
Until recently, some papers suggested that the distribution of the main L haplogroups in North Africa was mainly due to trans-Saharan slave trade.[46] However in September 2010, a thorough study about Berber mtDNA by Frigi et al. concluded that most of L haplogroups were much older and introduced by an ancient African gene flow around 20,000 years ago.[47]
Autosomal DNA
In a recent study by Jun Z. Li et al. 2008 that studied 938 unrelated individuals from 51 populations of the Human Genome Diversity Panel at 650,000 SNPs they found that "the Mozabite people from the northern Sahara bear contributions from sub-Saharan Africa, the Middle East, and Europe; this group in fact originates from the Middle East." (on average 55% Middle East, 25% European and 20% Sub-saharan).[48]
Influences on Europe and Latin America
According to a study in 2011, almost all Southern Europeans have inherited 1%–3% Sub-Saharan ancestry (3.2% in Portugal, 2.9% in Sardinia, 2.7% in Southern Italy, 2.4% in Spain and 1.1% in Northern Italy) with an average mixture date of around 55 generations ago, "consistent with North African gene flow at the end of the Roman Empire and subsequent Arab migrations".[49]
Iberia
In the Iberian Peninsula, North African male haplogroups, especially E1b1b1b (E-M81), E1b1b1a-b (M78 derived chromosomes showing the rare DYS439 allele 10) and a subset of J1 (M267 derived),[50] are found in significant amounts with an average frequency of about 7-8% in the peninsula with frequencies surpassing 10% in some regions, like 18.6% in Cantabria.[51][52][53][54]
- Historically introduced NW African types in Italy and Iberia (Capelli et al. (2009))
Sample N E1b1b1b E1b1b1a-b (DYS439 allele 10) J1 (subset) Total % Peninsular Italy 915 0.8 0.3 0.7 1.7 Sicily 93 2.2 2.2 3.2 7.5 Spain 717 5.2 1 1.5 7.7 Portugal 659 5 0.3 1.8 7.1 Iberia 1376 5.1 0.7 1.7 7.4 As an exceptional case in Europe, E-M81 has also been observed at 40% the Pasiegos from Cantabria.[55]
Concerning the level of male genetic admixture in Iberia, an important study by Adams et al. 2008 that analysed 1140 individuals in Iberia found a mean North African admixture of 10.6%, with wide geographical variation, ranging from 2.5% in Catalonia, 11.8% in North Portugal, 16.1% in South Portugal, 20.8% in Galicia to 21.7% in Northwest Castile.[53][56]
Iberian region %NW African male admixture Castile, NorthWest 21.7% Minorca 21.5% Galicia 20.8% Extremadura 19% Andalucia, West 16.7% Portugal, South 16.1% Valencia 12.8% Portugal, North 11.8% Asturias 10.5% Castile, NorthEast 9.3% Majorca 6.6% Aragon 4.8% Ibiza 3.8% Andalucia, East 2.4% Catalonia 2.3% Castilla 0.9% MtDna (female lineages) genetic studies on Iberian populations also show that North African mitochondrial DNA sequences (haplogroup U6) are found at much higher levels than those generally observed elsewhere in Europe. Although the overall absolute frequency of U6 is low (2.4%), this signals a possible current North African ancestry proportion of 8%–9%, because U6 is not a common lineage in North Africa itself. U6 reaches its highest frequency in North Portugal at about 4-6% where Gonzalez et al. 2003 estimated a possible North African ancestry proportion of 27%.[57][58][59]
Iberia is also the region in Europe with the highest frequency of the female mediated mtDNA haplogroup L of Sub-Saharan origin, likely a result of Berber and Arab colonization or African slave trade. Pereira et al. 2005, who analysed 1045 Iberian individuals, found sub-Saharan mtDNA L haplogroups at rates of 11.38% in south Portugal, 5.02% in Center Portugal, 3.21% in North Portugal and 3.26% in Galicia.[57] According to Alvarez et al. 2010 who found L haplogroups at a rate of 4.70% in the Spanish province of Zamora, "as the Hts found in the area are also shared with North African populations, we cannot discard the possibility that these lineages derived from the North African Muslim permanence in the Iberian Peninsula".[60] In another study, Casas et al. 2006 extracted DNA from human remains that were exhumed from historic burial sites in Al-Andalus, Spain (between 12th-13th century). The frequency of Sub-Saharan lineages detected in the medieval samples was 14.6% and 8.3% in the present population of Priego de Cordoba. The authors suggest both the Muslim occupation, and prehistoric migrations before the Muslim occupation would have been the source of these lineages.[61] Brehm at al. 2003 also found a significant Sub-Saharan imprint in the Autonomous regions of Portugal, with L haplogroups constituting about 13% of the lineages in Madeira and 3.4 % in the Azores.
Iberian region/NW African mtDna > 2% N %U6 %L Total Study Portugal, Alcacer do Sal 50 6.00% 22.00% 28.00% Pereira 2010[62] Spain, Canary islands (Avg) 300 14.00% 6.60% 20.60% Brehm 2003[63] Portugal, Madeira 155 3.90% 12.90% 16.80% Brehm 2003 Portugal, South 123 1.63% 11.38% 13.01% Pereira 2005[64] Portugal, South 203 0.49% 10.84% 11.33% Achilli 2007[65] Portugal, Coruche 160 0.62% 8.7% 9.32% Pereira 2010 Spain, Priego de Cordoba 108 0.93% 8.33% 9.26% Casas 2006[66] Portugal, Center 203 2.46% 6.40% 8.87% Achilli 2007 Portugal, North 187 5.35% 3.21% 8.56% Pereira 2005 South Iberian Peninsula 310 0.65% 7.42% 8.07% Casas 2006 Portugal, Center 239 2.51% 5.02% 7.53% Pereira 2005 Portugal, North 188 4.26% 3.19% 7.45% Achilli 2007 Spain, Galicia 92 2.17% 3.26% 5.43% Pereira 2005 Spain, Zamora 214 0.47% 4.67% 5.14% Alvarez 2010[67] Portugal, Açores 179 1.70% 3.40% 5.10% Brehm 2003 Spain, NorthWest 216 1.39% 3.70% 5.09% Achilli 2007 Spain, Center 148 4.05% 0.68% 4.73% Achilli 2007 Spain, NorthEast 118 1.69% 2.54% 4.24% Pereira 2005 Spain, multiple regions 312 1.28% 2.88% 4.16% CarlosAlvarez 2007[68] Portugal, Pias 75 0.00% 3.9% 3.9% Pereira 2010 Spain, Andalusia 114 1.75% 1.75% 3.51% Achilli 2007 Spain, Leon 61 1.64% 1.64% 3.28% Pereira 2005 Spain, Andalusia 65 1.54% 1.54% 3.08% Pereira 2005 Spain, NorthEast 179 1.12% 1.68% 2.79% Achilli 2007 Spain, Castile 38 2.63% 0.00% 2.63% Pereira 2005 Spain, Balearic islands 231 0.00% 2.16% 2.16% Picornell 2005[69] Canary Islands
In Canary Islands, a study by Nicole Maca-Meyer in 2003 found mtDna haplogroup U6 at rate of 14% in the present-day Canary Islands populations reflecting the Berber origin of the Guanches, the aboriginal population of the Canary Islands. In this study they compared aboriginal Guanche mtDNA (collected from Canarian archaeological sites) to that of today's Canarians and concluded that, "despite the continuous changes suffered by the population (Spanish colonization, slave trade), aboriginal mtDNA lineages constitute a considerable proportion [42–73%] of the Canarian gene pool".[70] MtDNA haplogroup L were also found at rate of 6.6%[71] and E-M81 at a rate of 8.28% with frequencies over 10% in the three largest islands of Tenerife (10.68%), Gran Canaria (11.54%) and Fuerteventura (13.33%). According to Fregel et al. 2009 the presence of autochthonous North African E-M81 lineages, and also other relatively abundant markers (E-M78 and J-M267) from the same region in the indigenous Guanche population, "strongly points to that area [North Africa] as the most probable origin of the Guanche ancestors". In this study, they estimated that, based on Y-chromosome and mtDNA haplogroup frequencies, the relative female and male indigenous Guanche contributions to the present-day Canary Islands populations were respectively of 41.8% and 16.1%.[72]
Canary Islands/NW African mtDna N %U6 %L Total Study La Gomera 46 50.01% 10.86% 60.87% Fregel 2009[73] El Hierro 32 21.88% 12.49% 34.37% Fregel 2009 Lanzarote 49 20.40% 8.16% 28.56% Fregel 2009 Gran Canaria 80 11.25% 10% 21.25% Fregel 2009 Tenerife 174 12.09% 7.45% 19.54% Fregel 2009 La Palma 68 17.65% 1.47% 19.12% Fregel 2009 Fuerteventura 42 16.66% 2.38% 19.04% Fregel 2009 An autosomal study in 2011 found an average Northwest African influence of about 17% in Canary Islanders with a wide interindividual variation ranging from 0% to 96%. According to the authors, the substantial Northwest African ancestry found for Canary Islanders supports that, despite the aggressive conquest by the Spanish in the 15th century and the subsequent immigration, genetic footprints of the first settlers of the Canary Islands persist in the current inhabitants. Paralleling mtDNA findings, the largest average Northwest African contribution was found for the samples from La Gomera.[74]
Canary Islands N Average NW African ancestry La Gomera 7 42.50% Fuerteventura 10 21.60% La Palma 7 21.00% El Hierro 7 19.80% Lanzarote 13 16.40% Tenerife 30 14.30% Gran Canaria 30 12.40% Total Canary Islanders 104 17.40% Italy
In Sicily, the contribution of North African populations is estimated to be about 6%-8% which shows a "genetic affinity between Sicily and North Africa".[54][75] In Italy,[76] North African haplogroups were found especially in a region of Southern Italy (East Campania, Northwest Apulia, Lucera) at frequency of 4.7% due to Frederick II’s relocation of Sicilian Muslims in the city of Lucera in the 13th century.[54] Haplogroup U6 have also been detected in Sicily and Southern Italy at very low levels.[77]
Latin America
As a consequence of Spanish and Portuguese colonization of Latin America, North African haplogroups are also found throughout Latin America especially in Brazil and Cuba where frequencies surpass generally 5%.[78][79][80] and among Hispanic men in USA.[81]
According to Fregel et al. (2009), the fact that male North African E-M81 and female U6 lineages from the Canaries have been detected in Cuba and Iberoamerica, demonstrates that Canary Islanders with indigenous Guanche ancestors actively participated in the American colonization.[82]
Other regions
In other countries, North African haplogroups can be found in France, Sudan, Somalia, Jordan (4%),[83] Lebanon and amongst Sephardi Jews.
Linguistics
The Maghreb have always been a multilingual region. Two thousand years ago, Punic, Latin and Berber alternated in communication among the populations of the Western parts of North Africa. The Arabic language arrived in the Maghreb region with the Arab conquest and Islam. This language ousted the Romances languages, although the process was a long time one : Romance language islets still existed in the Maghreb in the 12th century. The Maghreb once again became partly Romance with colonisation. From the 1830s, the French began by conquering Algeria, where French was declared the official language of the country. It also obtains the position of highly placed languages of local elites. In today's Maghreb, only Arabic possesses the status of official language. In spite of that, French is doing well in the region at the start of the 21st century.
See also
- Arabs
- Berbers
- Maghreb Jews
- Northwest Africa
- Carthage empire
- List of Maghrebis
- E1b1b1b (Y-DNA)
References and notes
- ^ without Ceuta, Melilla
- ^ "Estimé à six millions d'individus, l'histoire de leur enracinement, processus toujours en devenir, suscite la mise en avant de nombreuses problématiques...", « Être Maghrébins en France » in Les Cahiers de l’Orient, n° 71, troisième trimestre 2003
- ^ Maghreb people represent 45% of people born in arab countries who emigrated to Europe and N.America, they are 41% of the all Immigrants in Europe
- ^ css.escwa.org
- ^ Smail Chadli, Afrique du Nord: Anthropologie Génétique et Histoire du peuplement Humain, Anthropologie Génétique et Histoire du peuplement Humain. Antropo, 20, 41-48
- ^ Esperanza Alfonso, Islamic culture through Jewish eyes al-Andalus from the tenth to twelfth century, Routledge, 2007, p.104
- ^ Michèle Tribalat , « Mariages « mixtes » et immigration en France », Espace populations sociétés [En ligne] , 2009/2 | 2009 , mis en ligne le 01 avril 2011
- ^ Carolyn Burke. No Regrets: The Life of Edith Piaf, Bloomsbury Publishing, 2011, p.5
- ^ Michèle Tribalat, Revue Commentaire, juin 2009, n°127
- ^ Michèle Tribalat, Les yeux grands fermés, Denoël, 2010
- ^ Robert Castel, La discrimination négative, Paris, La République des idées/Seuil, 2007
- ^ Drouet, Jean-Baptiste; Alex Masson (December 2008). "Culture Le cinéma français est-il raciste ?" (in French). Première: 75–78. http://bworldconnection.com/culture.html?idA=175&rub=Culture.
- ^ Marie-Claude Chamla in Physical Anthropology of European Populations, Mouton, 1980, p.264: "Basically, there are three main types to be found (...). The Mediterranean element is always the major one making up about three-quarters of the population , and it appears to have three recognizable variants: (1) an Ibero-insular type (...); (2) an Atlanto-Mediterranean type (...); (3) finally, a type called "Saharan", rather infrequent (...). A second element which is fundamental but not widespread has been classed as Alpine by certain authors. (...) They constitute about one-tenth of the population, but it does not seem that they can be confused with the European Alpine type (...). A third element with Armenoid ties characterizes less than ten percent of the subjects (...). Beside these classes, some traces of the ancient Mechta-Afalou type can be found (...)."
- ^ Marie-Claude Chamla in Physical Anthropology of European Populations, Mouton, 1980, p.265-66 :"Green or light chestnut-colored eyes can frequently be found in the mountains areas (Kabylie and especially aures) and in the high plains of the east. This relative frequency of "mixed" colored eyes is not peculiar to Algerians but is apparent in other countries of North Africa as well, especially in Morocco (...) The frequency of pale-colored eyes (blue and gray), varies from two to fifteen percent according the region concerned"
- ^ a b c Coudray C, Olivieri A, Achilli A, et al. (March 2009). "The Complex and Diversified Mitochondrial Gene Pool of Berber Populations". Annals of Human Genetics 73 (2): 196–214. doi:10.1111/j.1469-1809.2008.00493.x. ISSN 0003-4800. PMID 19053990.
- ^ combined (Semino et al. 2004 30%) & (Arredi et al. 2004 32%)
- ^ Alshamali F, Pereira L, Budowle B, Poloni ES, Currat M (2009). "Local population structure in Arabian Peninsula revealed by Y-STR diversity". Hum. Hered. 68 (1): 45–54. doi:10.1159/000210448. PMID 19339785. http://content.karger.com/ProdukteDB/produkte.asp?doi=10.1159/000210448.
- ^ a b *Alshamali et al. 2009 81% (84/104) *Malouf et al. 2008: 70% (28/40) *Cadenas et al. 2008:45/62 = 72.6% J1-M267
- ^ Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample
- ^ Bosch E, Calafell F, Comas D, et al. (April 2001). "High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula". The American Journal of Human Genetics 68 (4): 1019–29. doi:10.1086/319521. ISSN 0002-9297. PMC 1275654. PMID 11254456. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1275654.
- ^ Nebel A, Landau-Tasseron E, Filon D, et al. (June 2002). "Genetic Evidence for the Expansion of Arabian Tribes into the Southern Levant and North Africa". The American Journal of Human Genetics 70 (6): 1594–6. doi:10.1086/340669. ISSN 0002-9297. PMC 379148. PMID 11992266. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=379148.
- ^ Semino O, Magri C, Benuzzi G, et al. (May 2004). "Origin, Diffusion, and Differentiation of Y-Chromosome Haplogroups E and J: Inferences on the Neolithization of Europe and Later Migratory Events in the Mediterranean Area". The American Journal of Human Genetics 74 (5): 1023–34. doi:10.1086/386295. ISSN 0002-9297. PMC 1181965. PMID 15069642. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1181965.
- ^ a b Arredi B, Poloni ES, Paracchini S, et al. (August 2004). "A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa". The American Journal of Human Genetics 75 (2): 338–345. doi:10.1086/423147. ISSN 0002-9297. PMC 1216069. PMID 15202071. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1216069.
- ^ a b Cruciani F, La Fratta R, Santolamazza P, et al. (May 2004). "Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa". The American Journal of Human Genetics 74 (5): 1014–22. doi:10.1086/386294. ISSN 0002-9297. PMC 1181964. PMID 15042509. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1181964.
- ^ a b Robino C, Crobu F, Di Gaetano C, et al. (May 2008). "Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample". International Journal of Legal Medicine 122 (3): 251–5. doi:10.1007/s00414-007-0203-5. ISSN 0937-9827. PMID 17909833.
- ^ Onofri V, Alessandrini F, Turchi C, et al. (August 2008). "Y-chromosome markers distribution in Northern Africa: High-resolution SNP and STR analysis in Tunisia and Morocco populations". Forensic Science International Genetics Supplement Series 1 (1): 235–6. doi:10.1016/j.fsigss.2007.10.173.
- ^ Ennafaa et al. (2011)
- ^ Robino C, Crobu F, Di Gaetano C, et al. (May 2008). "Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample". International Journal of Legal Medicine 122 (3): 251–5. doi:10.1007/s00414-007-0203-5. PMID 17909833.
- ^ Arredi B, Poloni ES, Paracchini S, et al. (August 2004). "A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa". American Journal of Human Genetics 75 (2): 338–45. doi:10.1086/423147. PMC 1216069. PMID 15202071. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1216069.
- ^ Ennafaa; Fregel; Khodjet-el-khil; Gonzalez (2011), "Mitochondrial DNA and Y-chromosome microstructure in Tunisia", European Journal of Human Genetics, doi:10.1038/jhg.2011.92, PMID 21833004, http://www.nature.com/jhg/journal/vaop/ncurrent/full/jhg201192a.html
- ^ Fadhlaoui-Zid, K., Martinez-Cruz, B., Khodjet-el-khil, H., Mendizabal, I., Benammar-Elgaaied, A. and Comas, D. (2011), Genetic structure of Tunisian ethnic groups revealed by paternal lineages. American Journal of Physical Anthropology. doi: 10.1002/ajpa.21581
- ^ Achilli A, Rengo C, Battaglia V, et al. (May 2005). "Saami and Berbers—An Unexpected Mitochondrial DNA Link". The American Journal of Human Genetics 76 (5): 883–6. doi:10.1086/430073. ISSN 0002-9297. PMC 1199377. PMID 15791543. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1199377.
- ^ Brakez Z, Bosch E, Izaabel H, et al. (May–June 2001). "Human mitochondrial DNA sequence variation in the Moroccan population of the Souss area". Annals of Human Biology 28 (3): 295–307. doi:10.1080/030144601300119106. ISSN 0301-4460. PMID 11393336.
- ^ Cherni L, Loueslati BY, Pereira L, et al. (February 2005). "Female Gene Pools of Berber and Arab Neighboring Communities in Central Tunisia: Microstructure of mtDNA Variation in North Africa". Human Biology 77 (1): 61–70. doi:10.1353/hub.2005.0028. ISSN 0018-7143. PMID 16114817.
- ^ Fadhlaoui-Zid, K; Plaza, S; Calafell, F; Ben Amor, M; Comas, D; Bennamar El Gaaied, A; Gaaied, El (May 2004). "Mitochondrial DNA Heterogeneity in Tunisian Berbers". Annals of Human Genetics 68 (Pt 3): 222–33. doi:10.1046/j.1529-8817.2004.00096.x. ISSN 0003-4800. PMID 15180702. http://freepages.genealogy.rootsweb.ancestry.com/~genealogiadelamaza/PDF/Bereberes.pdf.
- ^ Krings, M; Salem, A; Bauer, K; Geisert, H; Malek, A; Chaix, L; Simon, C; Welsby, D et al. (1999). "mtDNA Analysis of Nile River Valley Populations: A Genetic Corridor or a Barrier to Migration?". The American Journal of Human Genetics 64 (4): 1166–76. doi:10.1086/302314. PMC 1377841. PMID 10090902. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1377841.
- ^ Loueslati et al. 2006[verification needed]
- ^ Macaulay, V; Richards, M; Hickey, E; Vega, E; Cruciani, F; Guida, V; Scozzari, R; Bonné-Tamir, B et al. (Jan 1999). "The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs". The American Journal of Human Genetics 64 (1): 232–49. doi:10.1086/302204. ISSN 0002-9297. PMC 1377722. PMID 9915963. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1377722.
- ^ Olivieri, A.; Achilli, A; Pala, M; Battaglia, V; Fornarino, S; Al-Zahery, N; Scozzari, R; Cruciani, F et al. (Dec 2006). "The mtDNA Legacy of the Levantine Early Upper Palaeolithic in Africa". Science 314 (5806): 1767–70. Bibcode 2006Sci...314.1767O. doi:10.1126/science.1135566. ISSN 0036-8075. PMID 17170302.
- ^ Plaza, S.; Calafell, F; Helal, A; Bouzerna, N; Lefranc, G; Bertranpetit, J; Comas, D (2003). "Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean". Annals of Human Genetics 67 (Pt 4): 312–28. doi:10.1046/j.1469-1809.2003.00039.x. PMID 12914566. http://freepages.genealogy.rootsweb.ancestry.com/~genealogiadelamaza/PDF/Desde_los_pilares_de_Hercules.pdf.
- ^ Rando, JC; Pinto, F; González, AM; Hernández, M; Larruga, JM; Cabrera, VM; Bandelt, HJ (Nov 1998). "Mitochondrial DNA analysis of Northwest African populations reveals genetic exchanges with European, Near-Eastern, and sub-Saharan populations". Annals of Human Genetics 62 (Pt 6): 531–50. doi:10.1046/j.1469-1809.1998.6260531.x. ISSN 0003-4800. PMID 10363131.
- ^ Stevanovitch, A.; Gilles, A; Bouzaid, E; Kefi, R; Paris, F; Gayraud, RP; Spadoni, JL; El-Chenawi, F et al. (2004). "Mitochondrial DNA Sequence Diversity in a Sedentary Population from Egypt". Annals of Human Genetics 68 (Pt 1): 23–39. doi:10.1046/j.1529-8817.2003.00057.x. PMID 14748828.
- ^ Coudray, C; Olivieri, A; Achilli, A; Pala, M; Melhaoui, M; Cherkaoui, M; El-Chennawi, F; Kossmann, M et al. (Mar 2009). "The Complex and Diversified Mitochondrial Gene Pool of Berber Populations". Annals of Human Genetics 73 (2): 196–214. doi:10.1111/j.1469-1809.2008.00493.x. ISSN 0003-4800. PMID 19053990.
- ^ a b Cherni, L; Fernandes, V; Pereira, JB; Costa, MD; Goios, A; Frigi, S; Yacoubi-Loueslati, B; Amor, MB et al. (Jun 2009). "Post-last glacial maximum expansion from Iberia to North Africa revealed by fine characterization of mtDNA H haplogroup in Tunisia". American Journal of Physical Anthropology 139 (2): 253–60. doi:10.1002/ajpa.20979. ISSN 0002-9483. PMID 19090581.
- ^ Ottoni C, Primativo G, Hooshiar Kashani B, Achilli A, Martínez-Labarga C et al. (2010). "Mitochondrial Haplogroup H1 in North Africa: An Early Holocene Arrival from Iberia". PLoS ONE 5 (10): e13378. Bibcode 2010PLoSO...513378O. doi:10.1371/journal.pone.0013378. http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0013378.
- ^ Harich et .al 2010, The trans-Saharan slave trade - clues from interpolation analyses and high-resolution characterization of mitochondrial DNA lineages
- ^ Frigi et. al 2010, Ancient Local Evolution of African mtDNA Haplogroups in Tunisian Berber Populations, Human Biology, Volume 82, Number 4, August 2010
- ^ Li, J. Z.; Absher, DM; Tang, H; Southwick, AM; Casto, AM; Ramachandran, S; Cann, HM; Barsh, GS et al. (Feb 2008). "Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation". Science 319 (5866): 1100–4. Bibcode 2008Sci...319.1100L. doi:10.1126/science.1153717. ISSN 0036-8075. PMID 18292342.
- ^ Moorjani P, Patterson N, Hirschhorn JN, Keinan A, Hao L et al. (2011). "The History of African Gene Flow into Southern Europeans, Levantines, and Jews". PLoS Genet 7 (4): e1001373. doi:10.1371/journal.pgen.1001373. http://www.plosgenetics.org/article/info%3Adoi%2F10.1371%2Fjournal.pgen.1001373.
- ^ Capelli et al. 2008
- ^ Flores, C; Maca-Meyer, N; González, AM; Oefner, PJ; Shen, P; Pérez, JA; Rojas, A; Larruga, JM et al. (Oct 2004). "Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: implications for population demography" (Free full text). European Journal of Human Genetics 12 (10): 855–63. doi:10.1038/sj.ejhg.5201225. ISSN 1018-4813. PMID 15280900.
- ^ Beleza, S; Gusmão, L; Lopes, A; Alves, C; Gomes, I; Giouzeli, M; Calafell, F; Carracedo, A et al. (Mar 2006). "Micro-Phylogeographic and Demographic History of Portuguese Male Lineages". Annals of Human Genetics 70 (Pt 2): 181–94. doi:10.1111/j.1529-8817.2005.00221.x. ISSN 0003-4800. PMID 16626329.
- ^ a b Adams, SM; Bosch, E; Balaresque, PL; Ballereau, SJ; Lee, AC; Arroyo, E; López-Parra, AM; Aler, M et al. (Dec 2008). "The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula". The American Journal of Human Genetics 83 (6): 725–36. doi:10.1016/j.ajhg.2008.11.007. ISSN 0002-9297. PMC 2668061. PMID 19061982. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2668061.
- ^ a b c Capelli, C; Onofri, V; Brisighelli, F; Boschi, I; Scarnicci, F; Masullo, M; Ferri, G; Tofanelli, S et al. (Jun 2009). "Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe". European Journal of Human Genetics 17 (6): 848–52. doi:10.1038/ejhg.2008.258. ISSN 1018-4813. PMC 2947089. PMID 19156170. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2947089.
- ^ Cruciani, F; La Fratta, R; Santolamazza, P; Sellitto, D; Pascone, R; Moral, P; Watson, E; Guida, V et al. (May 2004). "Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa". The American Journal of Human Genetics 74 (5): 1014–22. doi:10.1086/386294. ISSN 0002-9297. PMC 1181964. PMID 15042509. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1181964.
- ^ "The study shows that religious conversions and the subsequent marriages between people of different lineage had a relevant impact on modern populations both in Spain, especially in the Balearic Islands, and in Portugal", The religious conversions of Jews and Muslims have had a profound impact on the population of the Iberian Peninsula, Elena Bosch, 2008
- ^ a b Pereira, Luisa; Cunha, Carla; Alves, Cintia; Amorim, Antonio (2005). "African Female Heritage in Iberia: A Reassessment of mtDNA Lineage Distribution in Present Times". Human Biology 77 (2): 213–29. doi:10.1353/hub.2005.0041. PMID 16201138.
- ^ Plaza, S.; Calafell, F; Helal, A; Bouzerna, N; Lefranc, G; Bertranpetit, J; Comas, D (2003). "Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean". Annals of Human Genetics 67 (Pt 4): 312–28. doi:10.1046/j.1469-1809.2003.00039.x. PMID 12914566.
- ^ González, AM; Brehm, A; Pérez, JA; Maca-Meyer, N; Flores, C; Cabrera, VM (Apr 2003). "Mitochondrial DNA affinities at the Atlantic fringe of Europe". American Journal of Physical Anthropology 120 (4): 391–404. doi:10.1002/ajpa.10168. ISSN 0002-9483. PMID 12627534.
- ^ Alvarez L, Santos C, Ramos A, Pratdesaba R, Francalacci P, Aluja MP (February 2010). "Mitochondrial DNA patterns in the Iberian Northern plateau: Population dynamics and substructure of the Zamora province". American Journal of Physical Anthropology 142 (4): NA. doi:10.1002/ajpa.21252. PMID 20127843.
- ^ Casas MJ, Hagelberg E, Fregel R, Larruga JM, González AM (December 2006). "Human mitochondrial DNA diversity in an archaeological site in al-Andalus: genetic impact of migrations from North Africa in medieval Spain". American Journal of Physical Anthropology 131 (4): 539–51. doi:10.1002/ajpa.20463. PMID 16685727.
- ^ Pereira V, Gomes V, Amorim A, Gusmão L, João Prata M. Genetic characterization of uniparental lineages in populations from Southwest Iberia with past malaria endemicity Am J Hum Biol. 2010 Sep-Oct;22(5):588-95.
- ^ A. Brehm, L. Pereira, T. Kivisild, and A. Amorim. Mitochondrial portraits of the madeira and açores archipelagos witness different genetic pools of its settlers. Hum Genet, 114(1):77–86, December 2003.
- ^ Pereira, Luisa. Cunha, Carla. Alves, Cintia. Amorim, António, African Female Heritage in Iberia: A Reassessment of mtDNA Lineage Distribution in Present Times. Human Biology - Volume 77, Number 2, April 2005, pp. 213-229
- ^ Alessandro Achilli, Anna Olivieri, Mitochondrial DNA Variation of Modern Tuscans Supports the Near Eastern Origin of Etruscans Am J Hum Genet. 2007 April; 80(4): 759–768. Published online 2007 February 6. PMCID: PMC1852723
- ^ Casas MJ, Hagelberg E, Fregel R, Larruga JM, Gonzalez AM. Human mitochondrial DNA diversity in an archaeological site in al-Andalus: genetic impact of migrations from North Africa in medieval Spain. Am J Phys Anthropol. 2006;131:539–551. doi: 10.1002/ajpa.20463
- ^ Alvarez L, Santos C, Ramos A, Pratdesaba R, Francalacci P, Aluja MP. Mitochondrial DNA patterns in the Iberian Northern plateau: population dynamics and substructure of the Zamora province. Am J Phys Anthropol. 2010 Aug;142(4):531-9
- ^ Alvarez JC, Johnson DL, Lorente JA, Martinez-Espin E, Martinez-Gonzalez LJ, Allard M, Wilson MR, Budowle B.Characterization of human control region sequences for Spanish individuals in a forensic mtDNA data set. Leg Med (Tokyo). 2007 Nov;9(6):293-304. Epub 2007 Jul 5
- ^ Picornell A, Gómez-Barbeito L, Tomàs C, Castro JA, Ramon MM. Mitochondrial DNA HVRI variation in Balearic populations. Am J Phys Anthropol. 2005 Sep;128(1):119-30
- ^ Maca-Meyer, N; Arnay, M; Rando, JC; Flores, C; González, AM; Cabrera, VM; Larruga, JM (Feb 2004). "Ancient mtDNA analysis and the origin of the Guanches" (Free full text). European Journal of Human Genetics 12 (2): 155–62. doi:10.1038/sj.ejhg.5201075. ISSN 1018-4813. PMID 14508507.
- ^ Brehm, A; Pereira, L; Kivisild, T; Amorim, A (Dec 2003). "Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlers". Human Genetics 114 (1): 77–86. doi:10.1007/s00439-003-1024-3. ISSN 0340-6717. PMID 14513360.
- ^ Fregel R, Gomes V, Gusmão L, et al. (2009). "Demographic history of Canary Islands male gene-pool: replacement of native lineages by European". BMC Evolutionary Biology 9: 181. doi:10.1186/1471-2148-9-181. PMC 2728732. PMID 19650893. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2728732.
- ^ Fregel et al.(2009) The maternal aborigine colonization of La Palma (Canary Islands) Euro J Hum Gen 17:1314-1324
- ^ Pino-Yanes M, Corrales A, Basaldúa S, Hernández A, Guerra L et al. (2011). "North African Influences and Potential Bias in Case-Control Association Studies in the Spanish Population". PLoS ONE 6 (3): e18389. Bibcode 2011PLoSO...6E8389P. doi:10.1371/journal.pone.0018389. http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0018389.
- ^ Di Gaetano, C; Cerutti, N; Crobu, F; Robino, C; Inturri, S; Gino, S; Guarrera, S; Underhill, PA et al. (Jan 2009). "Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome". European Journal of Human Genetics 17 (1): 91–9. doi:10.1038/ejhg.2008.120. ISSN 1018-4813. PMC 2985948. PMID 18685561. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2985948.
- ^ Cruciani, F.; La Fratta, R; Trombetta, B; Santolamazza, P; Sellitto, D; Colomb, EB; Dugoujon, JM; Crivellaro, F et al. (Jun 2007). "Tracing Past Human Male Movements in Northern/Eastern Africa and Western Eurasia: New Clues from Y-Chromosomal Haplogroups E-M78 and J-M12" (Free full text). Molecular Biology and Evolution 24 (6): 1300–11. doi:10.1093/molbev/msm049. ISSN 0737-4038. PMID 17351267. http://mbe.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=17351267.
- ^ Pertovaara, Antti; Kauppila, Timo; Mecke, Ernst (1991). "An Attempted Reversal of Cocaine-Induced Analgesia by Dexamethasone". Pharmacology & Toxicology 68: 93. doi:10.1111/j.1600-0773.1991.tb02042.x.
- ^ See the remarks of genetic genealogist Robert Tarín for example. We can add 6.1% (8 out of 132) in Cuba[unreliable source?]
- ^ Sener, S. F.; Imperato, JP; Chmiel, J; Fremgen, A; Sylvester, J (Jan 1989). "The Use of Cancer Registry Data to Study Preoperative Carcinoembryonic Antigen Level as an Indicator of Survival in Colorectal Cancer" (Free full text). CA a Cancer Journal for Clinicians 39 (1): 50–7. doi:10.3322/canjclin.39.1.50. ISSN 0007-9235. PMID 2492877. http://caonline.amcancersoc.org/cgi/pmidlookup?view=long&pmid=2492877.
- ^ Silva, DA; Carvalho, E; Costa, G; Tavares, L; Amorim, A; Gusmão, L (Nov 2006). "Y-chromosome genetic variation in Rio De Janeiro population". American Journal of Human Biology 18 (6): 829–37. doi:10.1002/ajhb.20567. ISSN 1042-0533. PMID 17039481.
- ^ Paracchini, S; Pearce, CL; Kolonel, LN; Altshuler, D; Henderson, BE; Tyler-Smith, C (Nov 2003). "A Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort study". Journal of Medical Genetics 40 (11): 815–9. doi:10.1136/jmg.40.11.815. ISSN 0022-2593. PMC 1735314. PMID 14627670. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1735314.
- ^ Rosa Fregel, Verónica Gomes, Leonor Gusmão, Ana M González , Vicente M Cabrera1 , António Amorim, Jose M Larruga et al. (2009) Demographic history of Canary Islands male gene-pool: replacement of native lineages by European BMC Evolutionary Biology 2009, 9:181doi:10.1186/1471-2148-9-181
- ^ Flores, C; Maca-Meyer, N; Larruga, JM; Cabrera, VM; Karadsheh, N; Gonzalez, AM (2005). "Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in Jordan". Journal of Human Genetics 50 (9): 435–41. doi:10.1007/s10038-005-0274-4. ISSN 1434-5161. PMID 16142507.
External links
- The African roots of Latin Christianity by Henri Teissier, Regional Bishop of North Africa
Categories:
Wikimedia Foundation. 2010.