Maghrebis
المغاربيون Al Māġāribiyyun
Regions with significant populations
Maghreb
 Algeria45,917,000[1]
 Morocco38,670,000[2]
 Tunisia12,135,000[3]
 Libya7,112,000[4][5][6]
 France5,326,000[7]
 Mauritania4,975,000[8]
 Israel750,000[9]-950,000[10]
 Canada[c]141,660[11]
Languages
Religion
Related ethnic groups
Berbers, Maghrebi Arabs, Maghrebi Jews, Tuareg, other Afroasiatic-speaking peoples

a Without Ceuta and Melilla.

Maghrebis or Maghrebians (Arabic: المغاربيون) is a modern Arabic term meaning "Westerners", mainly referring to the western part of the Arab world and North Africa.[13] Maghrebis are predominantly of Arab and Berber or mixed Arab-Berber origins.

Maghrebis were known in medieval times as the Roman Africans or Moors. The term Moor is derived from Mauri, the Roman name for the Berbers of Mauretania, land of the Moors, the Roman name for the western part of the Maghreb.

Religion

Historic records of religion in the Maghreb region show its gradual inclusion in the Classical World, with coastal colonies established first by Phoenicians, Greeks, and later extensive conquest and rule by the Romans. By the 2nd century common era, the area had become a centre of Latin-speaking Christianity. Both Roman settlers and Romanized Berbers 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 (c. 210 – 258); Saint Monica; her son the philosopher Augustine of Hippo (354 – 430); and Julia of Corsica (5th century). The region was a birthplace of many Christians movements like Arianism and Donatism, now cast-off.

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.[14]

During the seventh century, the region's peoples began their nearly total conversion to Islam. There was a small but thriving Local Jewish community, as well as a small Local Christian community. Most Muslims follow the Maliki school of Sunni Islam. 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 zawiyas traditionally helped proliferate basic literacy and knowledge of Islam in rural regions.

Recently, the Christian community of Berber or Arab descent has experienced significant growth, and conversions to Christianity, especially to Evangelicalism, is common in Algeria,[15] especially in the Kabylie,[16] Morocco[17] and Tunisia.[18] A 2015 study estimates 380,000 Muslims converted to Christianity in Algeria.[12]

Culture

Diaspora

France

Maghrebis have settled mainly in the industrial regions in France, especially in the Île-de-France and Mediterranean regions. Many famous French people like Édith Piaf,[19] Isabelle Adjani, Arnaud Montebourg, Alain Bashung, Dany Boon, Gérald Darmanin and many others have Maghrebi ancestry.

According to Michel Tribalat, a researcher at INED, there were more than 4.6 million people of Maghrebi origin (with at least one Maghrebi grandparent from Algeria, Morocco or Tunisia) living in France in 2011 (3 million in 1999).[20][21] Below is a table of population of Maghrebi origin in France in 2011, numbers are in thousands:

Country of origin (2011) Immigrants 1st generation born in France 2nd generation born in France (aged under 60 only) Total
Algeria 737 1 170 563 2 470
Morocco 679 698 130 1 507
Tunisia 246 280 129 655
Total Maghreb 1 662 2 148 821 4 631

Note: for second generation born in France only individuals under 60 are taken into account.

According to Institut national de la statistique et des études économiques (the French National Institute for Statistics and Economic Studies), 16% of newborns in France between 2006 and 2008 have at least one Maghrebi grandparent born in the Greater Maghreb.[22]

In 2005, the percentage of young people under 18 of Maghrebi origin (at least one immigrant parent) were about 7% in Metropolitan France, 12% in Île-de-France, 13% in Lyon, 21% in Perpignan, 22% in the department of Seine-Saint-Denis, 37% in 18th arrondissement of Paris and 40% in several arrondissements of Marseille.[23][24]

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, and between 150,000 and 300,000 people of Maghrebin origin live in Canada.[25][26]

Genetic evidence

The genetic proximity observed between the North-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.[27] A genetic study published in January 2012 stated that the indigenous Northwest African ancestry appears most closely related to populations outside of Africa but "divergence between Maghrebi peoples and Near Eastern/Europeans likely precedes the Holocene (>12,000 ya)."[28]

Y-chromosome DNA

The Y-chromosome genetic structure of the Maghreb population seems to be mainly modulated by geography. The Y-DNA Haplogroup E1b1b-M215 and J, which are common among Afroasiatic-speaking populations in Africa and the Middle East, are frequent in the Maghreb; especially the haplogroup E-M215 (formerly E1b1b1b, E-M81 and E3b1b) which is typical of the indigenous Berber populations. In some parts of Tunisia, E1b1b-M215 can peak at 100% of the population. Followed by Haplogroup J, especially Haplogroup J-M267[29] , which is typically Middle Eastern, which can reach frequencies of 40% in the region,[30][31] and has its highest density founded in the southwestern Arabian Peninsula,[31] Followed by Haplogroup R1[32] which is primarily concentrated in the Chad Basin, though it is also found in the Maghreb at lower frequencies. These Y-DNA haplogroups are observed in both Berber and Arabic speakers.

The Maghreb Y chromosome pool (including both Berber and Arabic-speaking populations) may be summarized as follows, where only two haplogroups E1b1b-M215 and J comprise generally more than 80% of the total chromosomes:[33][34][35][36][37][38][39]

  • E-M215 (mainly E-M81) (50–100%)
  • J (mainly J-M267) (0–45%)
  • R1b (0–15%)
  • Sub-Saharan and other haplogroups (0–8%)

Haplogroup E-Z827 is the most common Y haplogroup among Maghreb Berbers and Arabs, dominated by its subclade, E-M183. It is thought to have originated in Northwest Africa 14,200 years ago.[40] 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 Maghreb Arab groups (45% in Oran).[38] It can reach frequencies of up to 100% in the Greater 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.[41]

Population Nb A/B E(xE1b1b) E1b1b1 E-V68 E-M81 E-M123 F K G I J-M267 J-M172 R-M420 R-M343 Other Study
1 Algeria15605.78%0.64%6.4%44.23%1.28%3.85%0.64%0021.8%0.64%0.64%014.1%Bekada et al. (2013)[42]
2 Algeria/Oran10207.9%05.9%45.1%0000022.5%4.9%1%11.8%1%Robino et al. (2008)[43]
3 Algeria/Algiers3502.9%011.4%42.9%011.8%2.9%0022.9%5.7%000Arredi et al. (2004)[44]
4 Algeria/Kabyles, Tizi Ouzou19000047.4%10.5%10.5%00015.8%0015.8%0Arredi et al. (2004)
5 Algeria/Mozabites6704.5%01.5%86.6%1.5%001.5%01.5%003%0Dugoujon et al. (2009)[45]
6 Algeria/Reguibat60005%080%01.67%00010%0003.33%Bekada et al. (2015)[46]
7 Tunisia/Tunis14802%3.4%5.4%37.8%2.7%4.7%0.7%0032.4%3.4%0.7%6.1%0.7%Arredi et al. (2004)
8 Tunisia52009.6%15.4%32.7%01.9%1.9%0034.6%3.8%000Onofri et al. (2008)
9 Tunisia/Bou Omrane4005%05%87.5%02.5%00000000Ennafaa et al. (2011)[47]
10 Tunisia/Bou Saad40000092.5%000005%0002.5%Ennafaa et al. (2011)
11 Tunisia/Jerbian cosmopolitan462.2%0015.2%60.9%4.3%00008.7%2.2%4.3%2.2%0Ennafaa et al. (2011)
12 Tunisia/Jerbian Berbers4700017%76.6%04.25%2.1%0000000Ennafaa et al. (2011)
13 Tunisia/Chenini–Douiret Berbers270000100%0000000000Fadhlaoui-Zid et al. (2011)[48]
14 Tunisia/Sened Berbers35000065.7%02.9%00031.4%0000Fadhlaoui-Zid et al. (2011)
15 Tunisia/Jradou Berbers320000100%0000000000Fadhlaoui-Zid et al. (2011)
16 Tunisia/Andalusian Zaghouan320003.1%40.6%09.4%00043.8%3.1%000Fadhlaoui-Zid et al. (2011)
17 Tunisia/Cosmopolitan Tunis33003.0%6.0%54.5%3.0%6.0%03.0%024.2%0000Fadhlaoui-Zid et al. (2011)
18 Morocco76006.05%4.21%6.83%67.4%00.9%0.53%0.66%0.13%6.32%1.32%005.65%Bekada et al. (2013)
19 Morocco/Sous Berbers65000098.5%0000000000Reguig et al. (2014)[49]
20 Morocco/Amizmiz Valley333%6.1%03%84.8%3%000000000Alvarez et al. (2009)
21 Sahrawi89020.2%0059.55%0000020.22%0000Fregel et al. (2009)[50]
22 Libya/Tuaregs from Fezzan47042.5%0048.9%000000006.4%2.1%Ottoni et al. (2011)[51]

Mitochondrial DNA

Many studies[52][53][54][55][56][57][58][59][60][61][62][63][64] have attempted to describe the genetic diversity of North-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)[27]):

  • 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 North-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."[27] 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".[64]

According to an 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.[65]

Until recently, some papers suggested that the distribution of the main L haplogroups in North Africa was mainly due to trans-Saharan slave trade.[66] 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.[67]

Autosomal DNA

In an autosomal study in 2012 by Henn et al., the authors conclude that Northwest African populations retain a unique signature of early "Maghrebi" ancestry, but are not a homogeneous group and most display varying combinations of five distinct ancestries (Maghrebi, European, Near Eastern, eastern and western sub-Saharan Africa). The majority of their ancestry derives from populations outside of Africa and is the result of at least four distinct episodes:

  • ancient "back-to-Africa" gene flow prior to the Holocene
  • gene flow from Iberia and the Levant during the Neolithic
  • more recent gene flow from the Near East resulting in a longitudinal gradient
  • limited but very recent migrations from sub-Saharan Africa.

They observed two distinct, opposite gradients of ancestry: an east-to-west increase in likely autochthonous Northwest African ancestry likely derived from "back-to-Africa" gene flow more than 12,000 years ago and an east-to-west decrease in likely Near Eastern Arabic ancestry. The indigenous Northwest African ancestry is more frequent in populations with historical Berber ethnicity. They also find significant signatures of sub-Saharan African ancestry that vary substantially among populations. According to the authors "these sub-Saharan ancestries appear to be a recent introduction into Northwest African populations, dating to about 1,200 years ago in southern Morocco and about 750 years ago into Egypt, possibly reflecting the patterns of the trans-Saharan slave trade that occurred during this period".[68]

Admixture analysis

Recent genetic analysis of North African populations have found that, despite the complex admixture genetic background, there is an autochthonous genomic component which is likely derived from "back-to-Africa" gene flow older than 12,000 years ago (ya) (i.e., prior to the Neolithic migrations). This local population substratum seems to represent a genetic discontinuity with the earliest modern human settlers of North Africa (those with the Aterian industry) given the estimated ancestry is younger than 40,000 years ago. North Morocco, Libya and Egypt carry high proportions of European and Near Eastern ancestral components, whereas Tunisia and Saharawi are those populations with highest autochthonous Northwest African component.[69]

Average ancestry proportions in Northwest African populations - Not using Ancient DNA from North Africa (Sánchez-Quinto 2012)[70]
Population N Maghreb* Europe* Near East* Sub-Saharan Africa*
Algeria1939%27%16%18%
Tunisia1893%4%2%1%
Saharawi1855%17%10%18%
Morocco North1844%31%14%11%
Morocco South1644%13%10%33%
Libya1731%28%25%16%
Egypt1919%37%30%14%

*Ancestries are labeled according to the region where the component is the commonest.

Average ancestry proportions in Northwest African populations - Using Ancient DNA from North Africa (Serral-Vidal 2019)

According to a recent genetic study in 2019, North African populations have been found to be the result of admixture of extensive gene flow coming from four different geographical locations (North Africa itself (Iberomaurusian), Europe (Early European Farmer), Middle East and sub-Saharan Africa) and temporal sources (Palaeolithic migrations, Neolithization, Arabization, and recent migrations).[71]

PopIberomaurusian
(Taforalt)
Anatolia Neolithic

(EEF)

West Asian

(Levant Neolithic)

Sub-Saharan African
Saharawi37%34%18%11%
Moroccan30%38%19%14%
Berber-Moroccan28%47%17%8%
Berber-Mozabite26%43%18%13%
Algerian22%46%17%15%
Berber-Zenata22%27%12%39%
Libyan22%34%35%9%
Berber-Tunisian21%43%26%10%
Tunisian18%44%25%13%
Egyptian11%41%38%10%

Iberia

According to autosomal study in 2013 by Botigué et al. using genome-wide SNP data from over 2,000 individuals, the Northwest African admixture averages 10-12%.[72][73][74]

In the Iberian Peninsula, Northwest African male haplogroups, especially E1b1b1b (E-M81), E1b1b1a-b (M78 derived chromosomes showing the rare DYS439 allele 10 or E-V65) and a subset of J1 (M267 derived),[75] are found with an average frequency of about 7–8% in the peninsula with frequencies surpassing 10% in some regions, like 18.6% in Cantabria[76][77][78][79] with the exceptional case of Pasiegos (40%).[80]

The overall absolute frequency of U6 is low (2.4%), with its highest frequency in North Portugal at about 4-6%.[81][82][83] MtDNA haplogroup L of Sub-Saharan origin, likely as a result of Berber and Arab colonization or African slave trade, is found at rates of 11.38% in south Portugal, 5.02% in Center Portugal, 3.21% in North Portugal and 3.26% in Galicia.[81] and 4.70% in the Spanish province of Zamora,[84] with the highest incidence 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, Alcácer do Sal506.00%22.00%28.00%Pereira 2010[85]
Spain, Canary islands (Avg)30014.00%6.60%20.60%Brehm 2003[86]
Portugal, Madeira1553.90%12.90%16.80%Brehm 2003
Spain, Huelva (Andalusia)1358.86%5.70%14.56%Hernandez 2014[87]
Portugal, South1231.63%11.38%13.01%Pereira 2005[88]
Portugal, South2030.49%10.84%11.33%Achilli 2007[89]
Portugal, Coruche1600.62%8.7%9.32%Pereira 2010
Spain, Priego de Cordoba1080.93%8.33%9.26%Casas 2006[90]
Portugal, Center2032.46%6.40%8.87%Achilli 2007
Portugal, North1875.35%3.21%8.56%Pereira 2005
South Iberian Peninsula3100.65%7.42%8.07%Casas 2006
Portugal, Center2392.51%5.02%7.53%Pereira 2005
Portugal, North1884.26%3.19%7.45%Achilli 2007
Spain, Galicia922.17%3.26%5.43%Pereira 2005
Spain, Zamora2140.47%4.67%5.14%Alvarez 2010[91]
Portugal, Açores1791.70%3.40%5.10%Brehm 2003
Spain, NorthWest2161.39%3.70%5.09%Achilli 2007
Spain, Center1484.05%0.68%4.73%Achilli 2007
Spain, NorthEast1181.69%2.54%4.24%Pereira 2005
Spain, multiple regions3121.28%2.88%4.16%CarlosAlvarez 2007[92]
Portugal, Pias750.00%3.9%3.9%Pereira 2010
Spain, Andalusia1141.75%1.75%3.51%Achilli 2007
Spain, Granada (Andalusia)1172.48%0.83%3.31%Hernandez 2014
Spain, Leon611.64%1.64%3.28%Pereira 2005
Spain, Andalusia651.54%1.54%3.08%Pereira 2005
Spain, NorthEast1791.12%1.68%2.79%Achilli 2007
Spain, Castile382.63%0.00%2.63%Pereira 2005
Spain, Balearic islands2310.00%2.16%2.16%Picornell 2005[93]

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".[94] MtDNA haplogroup L were also found at rate of 6.6%[95] 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%.[96]

Canary Islands/
NW African mtDna
N %U6 %L Total Study
La Gomera4650.01%10.86%60.87%Fregel 2009[97]
El Hierro3221.88%12.49%34.37%Fregel 2009
Lanzarote4920.40%8.16%28.56%Fregel 2009
Gran Canaria8011.25%10%21.25%Fregel 2009
Tenerife17412.09%7.45%19.54%Fregel 2009
La Palma6817.65%1.47%19.12%Fregel 2009
Fuerteventura4216.66%2.38%19.04%Fregel 2009

An autosomal study in 2011 found an average North African influence of about 17% in Canary Islanders with a wide interindividual variation ranging from 0% to 96%. According to the authors, the substantial North African ancestry found for Canary Islanders supports that, despite the 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 North African contribution was found for the samples from La Gomera.[98]

Canary Islands N Average
NW African
ancestry
La Gomera742.50%
Fuerteventura1021.60%
La Palma721.00%
El Hierro719.80%
Lanzarote1316.40%
Tenerife3014.30%
Gran Canaria3012.40%
Total Canary Islanders10417.40%

Italy

A panel of 52 AIMs was genotyped in 435 Italian individuals[99] in order to estimate the proportion of ancestry from a three-way differentiation: Sub-Saharan África, Europe, and Asia. An autosomal basal proportion of Sub-Saharan ancestry is higher (9.2%, on average) than other central or northern European populations (1.5%, on average). The amount of African ancestry in Italians is however more comparable to (but slightly higher than) the average in other Mediterranean countries (7.1%).

An average mixture date of around 55 generations/1100 years ago was given, "consistent with North African gene flow at the end of the Roman Empire and subsequent Arab migrations".[100] In Sicily, the contribution of Northwest African populations is estimated to be about 6-8%, which shows a "genetic affinity between Sicily and Northwest Africa".[79][101] In Italy,[102] 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.[79] Haplogroup U6 have also been detected in Sicily and Southern Italy at very low levels.[103] In a 2014 study by Stefania Sarno et al. with 326 samples from Cosenza, Matera, Lecce and five Sicilian provinces, E-M81 shows an average frequency of 1.5%, but the typical Maghrebin core haplotype 13-14-30-24-9-11-13 has been found in only two out of the five E-M81 individuals.[104][105]

France

Haplogroup E-M81 is also found in some regions of France (excluding recent immigration as only men with French surnames were analysed). 2.70% (15/555) overall with frequencies surpassing 5% in Auvergne (5/89) and Île-de-France (5/91).

According to a genetic study in 2000 based on HLA, French from Marseilles "are more or less isolated from the other western European populations. They are in an intermediate position between the Northwest Africans (Algerians from Algiers and Oran; Tunisians) and the western Europeans populations (France, Spain, and Portugal)". According to the authors "these results cannot be attributed to recent events because of the knowledge of the grandparents' origin" in the sample. This study reveals "that the southern French population from Marseilles is related genetically to the southwestern Europeans and Northwest Africans, who are geographically close" and that "a substantial gene flow has thus probably been present among the populations of these neighboring areas".[106]

Latin America

As a consequence of Southern European colonization and immigration to Latin America, Northwest African haplogroups are also found throughout Latin America. In Brazil and Cuba frequencies surpass generally 5%.[107][108][109] and among Hispanic men in USA.[110]

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.[111]

Other regions

In other countries, Northwest African haplogroups can be found in France, Egypt, Sudan, Somalia, Jordan (4%),[112] Lebanon and amongst Sephardi Jews.

Linguistics

The Greater Maghreb have hosted several languages. Berber or also known as Amazigh is the indigenous language family of the region, belonging to the greater Afro-Asiatic family. Two thousand years ago, Punic, Berber and Latin would have alternated in communication among the populations of Northwest Africa and the rest of the Mediterranean basin. The Arabic language as known throughout the region nowadays arrived later in the Greater Maghreb with the historical Arab conquest and Islam. This language ousted the Berber languages in its various variants, although the process was a long time one, Berber has long been a very prominent language in Algeria and Morocco till our contemporary era. Romance language itself might still have existed in the Greater Maghreb in the 12th century. The Greater 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 Greater Maghreb, Modern Standard Arabic possesses the status of official language in all the region despite Maghrebi Arabic being the languages of most people.

The Berber language also has official status in Algeria and Morocco. While French is doing well in the region at the start of the 21st century.

English is becoming quite popular as a second language subject at schools across the Greater Maghreb.

Arabization

See also

References and notes

  1. "Algeria Population (LIVE)". 10 October 2021. Archived from the original on 23 February 2023. Retrieved 10 October 2021.
  2. "Morocco Population (2021) - Worldometer". Archived from the original on 26 October 2022. Retrieved 8 January 2021.
  3. CIA World Factbook. "Libya". Archived from the original on 9 January 2021. Retrieved 5 February 2013.
  4. "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
  5. 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
  6. "css.escwa.org" (PDF). Archived from the original (PDF) on 17 March 2012. Retrieved 9 July 2011.
  7. "Immigrés et descendants d'immigrés". Insee (in French). Archived from the original on 12 November 2022. Retrieved 12 November 2022.
  8. "1: Répartition spatiale de la population" (PDF). Recensement Général de la Population et de l'Habitat (RGPH) 2013 (Report) (in French). National Statistical Office of Mauritania. July 2015. p. v. Retrieved 20 December 2015.
  9. "Les Maghrebins en Israel" (in French). Archived from the original on 20 September 2021. Retrieved 14 May 2020.
  10. Sharaby, Rachel; Wenden, Catherine Wihtol de; Giovanella, Myrna (2008). "Les immigrés juifs maghrébins en Israël". Migrations Société (in French). 120 (6): 131–154. doi:10.3917/migra.120.0131. Archived from the original on 26 June 2020. Retrieved 14 May 2020.
  11. Statistics Canada (8 May 2013). "2011 National Household Survey: Data tables". Archived from the original on 24 December 2018. Retrieved 11 February 2014.
  12. 1 2 "Believers in Christ from a Muslim Background: A Global Census". Archived from the original on 31 January 2017. Retrieved 12 December 2015.
  13. "The Arab world". AMBergh Education. Archived from the original on 3 May 2019. Retrieved 17 March 2019. The North African part of the Arab World to the west of Egypt and Sudan is known as the Maghreb (gharb meaning west).
  14. Christianity in North Africa and West Asia. Hendrickson Publ. May 2020. ISBN 9781683072874.
  15. Lucien Oulahbib, Le monde arabe existe-t-il ?, page 12, 2005, Editions de Paris, Paris.
  16. "Morocco: General situation of Muslims who converted to Christianity, and specifically those who converted to Catholicism; their treatment by Islamists and the authorities, including state protection (2008-2011)". Archived from the original on 1 March 2019. Retrieved 12 December 2015.
  17. International Religious Freedom Report 2007: Tunisia Archived 9 March 2021 at the Wayback Machine. United States Bureau of Democracy, Human Rights, and Labor (14 September 2007). This article incorporates text from this source, which is in the public domain.
  18. Carolyn Burke. No Regrets: The Life of Edith Piaf, Bloomsbury Publishing, 2011, p.5
  19. Michèle Tribalat, « Mariages « mixtes » et immigration en France » Archived 14 September 2011 at the Wayback Machine, Espace populations sociétés [En ligne], 2009/2 | 2009, mis en ligne le 01 avril 2011
  20. Michèle Tribalat, « Une estimation des populations d'origine étrangère en France en 2011 », Espace populations sociétés, 2015/1-2, en ligne Archived 12 February 2017 at Wikiwix
  21. Les immigrés, les descendants d'immigrés et leurs enfants Archived 8 July 2012 at the Wayback Machine, Pascale Breuil-Genier, Catherine Borrel, Bertrand Lhommeau, Insee 2011
  22. Michèle Tribalat, Revue Commentaire, juin 2009, n°126, p.436
  23. Michèle Tribalat, Les yeux grands fermés, Denoël, 2010
  24. Robert Castel, La discrimination négative, Paris, La République des idées/Seuil, 2007
  25. Drouet, Jean-Baptiste; Alex Masson (December 2008). "Culture Le cinéma français est-il raciste ?". Première (in French): 75–78. Archived from the original on 14 December 2008. Retrieved 14 January 2009.
  26. 1 2 3 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. S2CID 21826485.
  27. Henn BM, Botigué LR, Gravel S, Wang W, Brisbin A, et al. (January 2012). Schierup MH (ed.). "Genomic Ancestry of North Africans Supports Back-to-Africa Migrations". PLOS Genetics. 8 (1): e1002397. doi:10.1371/journal.pgen.1002397. PMC 3257290. PMID 22253600.
  28. combined (Semino et al. 2004 30%) & (Arredi et al. 2004 32%)
  29. 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.
  30. 1 2
    • Alshamali et al. 2009 81% (84/104) *Malouf et al. 2008: 70% (28/40) *Cadenas et al. 2008:45/62 = 72.6% J1-M267
  31. 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". Int. J. Legal Med. 122 (3): 251–5. doi:10.1007/s00414-007-0203-5. PMID 17909833. S2CID 11556974.
  32. 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 North 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.
  33. 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.
  34. 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.
  35. 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.
  36. 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.
  37. 1 2 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. S2CID 11556974.
  38. 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.
  39. "E-M81 YTree". www.yfull.com. Archived from the original on 26 May 2019. Retrieved 21 July 2016.
  40. Ennafaa et al. (2011)
  41. Bekada, Asmahan; Fregel, Rosa; Cabrera, Vicente M.; Larruga, José M.; Pestano, José; Benhamamouch, Soraya; González, Ana M. (19 February 2013). "Introducing the Algerian Mitochondrial DNA and Y-Chromosome Profiles into the North African Landscape". PLOS ONE. 8 (2): e56775. Bibcode:2013PLoSO...856775B. doi:10.1371/journal.pone.0056775. ISSN 1932-6203. PMC 3576335. PMID 23431392.
  42. 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. S2CID 11556974.
  43. 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.
  44. Dugoujon J.M., Coudray C., Torroni A., Cruciani F., Scozzari F., Moral P., Louali N., Kossmann M. The Berber and the Berbers: Genetic and linguistic diversities. In: D'Errico, Francesco; Hombert, Jean Marie (2009). Becoming Eloquent: Advances in the Emergence of Language, Human Cognition, and Modern Cultures. John Benjamins Publishing. ISBN 978-90-272-3269-4.
  45. Bekada, Asmahan; Arauna, Lara R.; Deba, Tahria; Calafell, Francesc; Benhamamouch, Soraya; Comas, David (24 September 2015). "Genetic Heterogeneity in Algerian Human Populations". PLOS ONE. 10 (9): e0138453. Bibcode:2015PLoSO..1038453B. doi:10.1371/journal.pone.0138453. ISSN 1932-6203. PMC 4581715. PMID 26402429.
  46. Ennafaa; Fregel; Khodjet-el-khil; Gonzalez (2011), "Mitochondrial DNA and Y-chromosome microstructure in Tunisia", Journal of Human Genetics, 56 (10): 734–41, doi:10.1038/jhg.2011.92, PMID 21833004
  47. Fadhlaoui-Zid, K.; Martinez-Cruz, B.; Khodjet-el-khil, H.; Mendizabal, I.; Benammar-Elgaaied, A.; Comas, D. (2011). "Genetic structure of Tunisian ethnic groups revealed by paternal lineages". American Journal of Physical Anthropology. 146 (2): 271–80. doi:10.1002/ajpa.21581. PMID 21915847.
  48. Ahmed, Reguig; Nourdin, Harich; Abdelhamid, Barakat; Hassan, Rouba (1 January 2014). "Phylogeography of E1b1b1b-M81 Haplogroup and Analysis of its Subclades in Morocco". Human Biology Open Access Pre-Prints. 86 (2). Archived from the original on 22 July 2019. Retrieved 21 July 2016.
  49. Fregel, Rosa; Gomes, Verónica; Gusmão, Leonor; González, Ana M.; Cabrera, Vicente M.; Amorim, António; Larruga, Jose M. (3 August 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. ISSN 1471-2148. PMC 2728732. PMID 19650893.
  50. Ottoni C, Larmuseau MH, Vanderheyden N, Martínez-Labarga C, Primativo G, Biondi G, Decorte R, Rickards O (May 2011). "Deep into the roots of the Libyan Tuareg: a genetic survey of their paternal heritage". Am J Phys Anthropol. 145 (1): 118–24. doi:10.1002/ajpa.21473. PMID 21312181.
  51. 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.
  52. 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. S2CID 1970297.
  53. 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. hdl:10216/109267. ISSN 0018-7143. PMID 16114817. S2CID 7022459.
  54. 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" (PDF). Annals of Human Genetics. 68 (Pt 3): 222–33. doi:10.1046/j.1529-8817.2004.00096.x. ISSN 0003-4800. PMID 15180702. S2CID 6407058. Archived (PDF) from the original on 24 October 2012. Retrieved 3 September 2009.
  55. Krings, M; Salem, A; Bauer, K; Geisert, H; Malek, A; Chaix, L; Simon, C; Welsby, D; Dirienzo, A (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.
  56. Loueslati et al. 2006
  57. Macaulay, V; Richards, M; Hickey, E; Vega, E; Cruciani, F; Guida, V; Scozzari, R; Bonné-Tamir, B; Sykes, B (January 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.
  58. Olivieri, A.; Achilli, A; Pala, M; Battaglia, V; Fornarino, S; Al-Zahery, N; Scozzari, R; Cruciani, F; Behar, DM (December 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. S2CID 3810151.
  59. 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" (PDF). Annals of Human Genetics. 67 (Pt 4): 312–28. doi:10.1046/j.1469-1809.2003.00039.x. PMID 12914566. S2CID 11201992. Archived (PDF) from the original on 3 November 2012. Retrieved 3 September 2009.
  60. Rando, JC; Pinto, F; González, AM; Hernández, M; Larruga, JM; Cabrera, VM; Bandelt, HJ (November 1998). "Mitochondrial DNA analysis of North 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. S2CID 2925153.
  61. Stevanovitch, A.; Gilles, A; Bouzaid, E; Kefi, R; Paris, F; Gayraud, RP; Spadoni, JL; El-Chenawi, F; Béraud-Colomb, E (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. S2CID 44901197.
  62. Coudray, C; Olivieri, A; Achilli, A; Pala, M; Melhaoui, M; Cherkaoui, M; El-Chennawi, F; Kossmann, M; Torroni, A (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. S2CID 21826485.
  63. 1 2 Cherni, L; Fernandes, V; Pereira, JB; Costa, MD; Goios, A; Frigi, S; Yacoubi-Loueslati, B; Amor, MB; Slama, A (June 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.
  64. Ottoni C, Primativo G, Hooshiar Kashani B, Achilli A, Martínez-Labarga C, et al. (2010). Kayser M (ed.). "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. PMC 2958834. PMID 20975840.
  65. Harich (2010). "The trans-Saharan slave trade - clues from interpolation analyses and high-resolution characterization of mitochondrial DNA lineages". BMC Evolutionary Biology. 10: 138. doi:10.1186/1471-2148-10-138. PMC 2875235. PMID 20459715.
  66. Frigi; et al. (2010). "Ancient Local Evolution of African mtDNA Haplogroups in Tunisian Berber Populations". Human Biology. 82 (4): 367–84. doi:10.3378/027.082.0402. PMID 21082907. S2CID 27594333. Archived from the original on 4 March 2016. Retrieved 2 October 2010.
  67. Henn BM, Botigué LR, Gravel S, Wang W, Brisbin A, et al. (2012). "Genomic Ancestry of North Africans Supports Back-to-Africa Migrations". PLOS Genet. 8 (1): e1002397. doi:10.1371/journal.pgen.1002397. PMC 3257290. PMID 22253600.
  68. Sánchez-Quinto F, Botigué LR, Civit S, Arenas C, Ávila-Arcos MC, et al. (2012). "North African Populations Carry the Signature of Admixture with Neandertals". PLOS ONE. 7 (10): e47765. Bibcode:2012PLoSO...747765S. doi:10.1371/journal.pone.0047765. PMC 3474783. PMID 23082212.
  69. Sánchez-Quinto F et al. 2012
  70. Serra-Vidal et al. 2019, Heterogeneity in Palaeolithic Population Continuity and Neolithic Expansion in North Africa.
  71. "With the reassuring exception of the Basque population isolate, the Iberian Peninsula showed the greatest imprint. Specifically, southwestern European populations averaged between 4% and 20% of their genomes assigned to a Northwest African ancestral cluster, whereas this value did not exceed 2% in southeastern European populations. " Karl Skorecki and Doron M. Behar, North Africans traveling north Archived 23 October 2013 at the Wayback Machine PNAS 16 July 2013 vol. 110 no. 29 Karl Skorecki, 11668–11669
  72. Botigué, LR; et al. (2013). "Gene flow from North Africa contributes to differential human genetic diversity in southern Europe". Proc Natl Acad Sci USA. 110 (29): 11791–11796. Bibcode:2013PNAS..11011791B. doi:10.1073/pnas.1306223110. PMC 3718088. PMID 23733930.
  73. David Comas, one of the authors of the study: "La cifra del 20% sólo se da en Canarias, para el resto del país oscila entre el 10% y 12%", Los españoles somos los europeos con más genes magrebíes Archived 9 March 2014 at the Wayback Machine, Huffington post, 3 June 2013
  74. Capelli et al. 2008
  75. Flores, C; Maca-Meyer, N; González, AM; Oefner, PJ; Shen, P; Pérez, JA; Rojas, A; Larruga, JM; Underhill, PA (October 2004). "Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: implications for population demography". European Journal of Human Genetics. 12 (10): 855–63. doi:10.1038/sj.ejhg.5201225. ISSN 1018-4813. PMID 15280900.
  76. Beleza, S; Gusmão, L; Lopes, A; Alves, C; Gomes, I; Giouzeli, M; Calafell, F; Carracedo, A; Amorim, A (March 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. S2CID 4652154.
  77. Adams, SM; Bosch, E; Balaresque, PL; Ballereau, SJ; Lee, AC; Arroyo, E; López-Parra, AM; Aler, M; Grifo, MS (December 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. See Supplemental Data, p.33, "Table S2. Ancestry Proportions in Iberian Populations" Archived 9 April 2019 at the Wayback Machine
  78. 1 2 3 Capelli, C; Onofri, V; Brisighelli, F; Boschi, I; Scarnicci, F; Masullo, M; Ferri, G; Tofanelli, S; Tagliabracci, A (June 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.
  79. Cruciani, F; La Fratta, R; Santolamazza, P; Sellitto, D; Pascone, R; Moral, P; Watson, E; Guida, V; Colomb, EB (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.
  80. 1 2 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. hdl:10216/109268. PMID 16201138. S2CID 20901589.
  81. 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. S2CID 11201992.
  82. González, AM; Brehm, A; Pérez, JA; Maca-Meyer, N; Flores, C; Cabrera, VM (April 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.
  83. 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): 531–9. doi:10.1002/ajpa.21252. PMID 20127843.
  84. Pereira, V. N.; Gomes, V. N.; Amorim, A. N.; Gusmão, L.; João Prata, M. (September–October 2010). "Genetic characterization of uniparental lineages in populations from Southwest Iberia with past malaria endemicity". American Journal of Human Biology. 22 (5): 588–595. doi:10.1002/ajhb.21049. PMID 20737604. S2CID 23350335.
  85. Brehm A.; Pereira L.; Kivisild T.; Amorim A. (2003). "Mitochondrial portraits of the madeira and açores archipelagos witness different genetic pools of its settlers". Hum Genet. 114 (1): 77–86. doi:10.1007/s00439-003-1024-3. hdl:10400.13/3046. PMID 14513360. S2CID 8870699.
  86. Hernández, CL; Reales, G; Dugoujon, JM; Novelletto, A; Rodríguez, JN; Cuesta, P; Calderón, R (2014). "Human maternal heritage in Andalusia (Spain): its composition reveals high internal complexity and distinctive influences of mtDNA haplogroups U6 and L in the western and eastern side of region". BMC Genet. 15: 11. doi:10.1186/1471-2156-15-11. PMC 3905667. PMID 24460736.
  87. Pereira, Luisa; Cunha, Carla; Alves, Cintia; Amorim, António (2005). "African Female Heritage in Iberia: A Reassessment of mtDNA Lineage Distribution in Present Times". Human Biology. 77 (2): 213–229. doi:10.1353/hub.2005.0041. hdl:10216/109268. PMID 16201138. S2CID 20901589.
  88. Achilli, A; Olivieri, A, Pala, M, Metspalu, E, Fornarino, S, Battaglia, V, Accetturo, M, Kutuev, I, Khusnutdinova, E, Pennarun, E, Cerutti, N, Di Gaetano, C, Crobu, F, Palli, D, Matullo, G, Santachiara-Benerecetti, AS, Cavalli-Sforza, LL, Semino, O, Villems, R, Bandelt, HJ, Piazza, A, Torroni, A (April 2007). "Mitochondrial DNA variation of modern Tuscans supports the near eastern origin of Etruscans". American Journal of Human Genetics. 80 (4): 759–68. doi:10.1086/512822. PMC 1852723. PMID 17357081.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  89. Casas MJ, Hagelberg E, Fregel R, Larruga JM, Gonzalez AM (2006). "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. 131 (4): 539–551. doi:10.1002/ajpa.20463. PMID 16685727.
  90. Alvarez L, Santos C, Ramos A, Pratdesaba R, Francalacci P, Aluja MP (August 2010). "Mitochondrial DNA patterns in the Iberian Northern plateau: population dynamics and substructure of the Zamora province". Am J Phys Anthropol. 142 (4): 531–9. doi:10.1002/ajpa.21252. PMID 20127843.
  91. 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
  92. Picornell A, Gómez-Barbeito L, Tomàs C, Castro JA, Ramon MM (September 2005). "Mitochondrial DNA HVRI variation in Balearic populations". Am J Phys Anthropol. 128 (1): 119–30. doi:10.1002/ajpa.10423. PMID 15761883.
  93. Maca-Meyer, N; Arnay, M; Rando, JC; Flores, C; González, AM; Cabrera, VM; Larruga, JM (February 2004). "Ancient mtDNA analysis and the origin of the Guanches". European Journal of Human Genetics. 12 (2): 155–62. doi:10.1038/sj.ejhg.5201075. ISSN 1018-4813. PMID 14508507.
  94. Brehm, A; Pereira, L; Kivisild, T; Amorim, A (December 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. hdl:10400.13/3046. ISSN 0340-6717. PMID 14513360. S2CID 8870699.
  95. 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.
  96. Fregel; et al. (2009). "The maternal aborigine colonization of La Palma (Canary Islands)". Eur J Hum Genet. 17 (10): 1314–1324. doi:10.1038/ejhg.2009.46. PMC 2986650. PMID 19337312.
  97. Pino-Yanes M, Corrales A, Basaldúa S, Hernández A, Guerra L, et al. (2011). O'Rourke D (ed.). "North African Influences and Potential Bias in Case-Control Association Studies in the Spanish Population". PLOS ONE. 6 (3): e18389. Bibcode:2011PLoSO...618389P. doi:10.1371/journal.pone.0018389. PMC 3068190. PMID 21479138.
  98. Sanchez JJ, Phillips C, Børsting C, Balogh K, Bogus M, Fondevila M, et al. (May 2006). "A multiplex assay with 52 single nucleotide polymorphisms for human identification". Electrophoresis. 27 (9): 1713–1724. doi:10.1002/elps.200500671. PMID 16586411. S2CID 5993654.
  99. Moorjani P, Patterson N, Hirschhorn JN, Keinan A, Hao L, Atzmon G, Burns E, Ostrer H, Price AL, Reich D (April 2011). McVean G (ed.). "The history of African gene flow into Southern Europeans, Levantines, and Jews". PLOS Genetics. 7 (4): e1001373. doi:10.1371/journal.pgen.1001373. PMC 3080861. PMID 21533020.
  100. Di Gaetano, C; Cerutti, N; Crobu, F; Robino, C; Inturri, S; Gino, S; Guarrera, S; Underhill, PA; King, RJ (January 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.
  101. Cruciani, F.; La Fratta, R; Trombetta, B; Santolamazza, P; Sellitto, D; Colomb, EB; Dugoujon, JM; Crivellaro, F; Benincasa, T (June 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. Archived from the original on 18 July 2012. Retrieved 8 September 2009.
  102. Pertovaara, Antti; Kauppila, Timo; Mecke, Ernst (1991). "An Attempted Reversal of Cocaine-Induced Analgesia by Dexamethasone". Pharmacology & Toxicology. 68 (2): 93–95. doi:10.1111/j.1600-0773.1991.tb02042.x. PMID 1852723.
  103. Di Gaetano et al. 2009
  104. Sarno, S; Boattini, A; Carta, M; Ferri, G; Alù, M; Yao, DY; Ciani, G; Pettener, D; Luiselli, D (2014). "An Ancient Mediterranean Melting Pot: Investigating the Uniparental Genetic Structure and Population History of Sicily and Southern Italy". PLOS ONE. 9 (4): e96074. Bibcode:2014PLoSO...996074S. doi:10.1371/journal.pone.0096074. PMC 4005757. PMID 24788788. This article contains quotations from this source, which is available under a Creative Commons Attribution 4.0 International (CC BY 4.0) license Archived 16 October 2017 at the Wayback Machine.
  105. Gibert M, Reviron D, Mercier P, Chiaroni J, Boetsch G (September 2000). "HLA-DRB1 and DQB1 polymorphisms in southern France and genetic relationships with other Mediterranean populations". Hum Immunol. 61 (9): 930–6. doi:10.1016/S0198-8859(00)00158-0. PMID 11053637.
  106. See the remarks Archived 10 December 2018 at the Wayback Machine of genetic genealogist Robert Tarín for example. We can add 6.1% (8 out of 132) in Cuba
  107. Sener, S. F.; Imperato, JP; Chmiel, J; Fremgen, A; Sylvester, J (January 1989). "The Use of Cancer Registry Data to Study Preoperative Carcinoembryonic Antigen Level as an Indicator of Survival in Colorectal Cancer". CA – A Cancer Journal for Clinicians. 39 (1): 50–7. doi:10.3322/canjclin.39.1.50. ISSN 0007-9235. PMID 2492877. S2CID 36182823.
  108. Silva, DA; Carvalho, E; Costa, G; Tavares, L; Amorim, A; Gusmão, L (November 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. S2CID 23778828.
  109. Paracchini, S; Pearce, CL; Kolonel, LN; Altshuler, D; Henderson, BE; Tyler-Smith, C (November 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.
  110. Fregel, Rosa; Gomes, Verónica; Gusmão, Leonor; González, Ana M; Cabrera, Vicente M; Amorim, António; Larruga, Jose M; 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.
  111. 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.
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