Archive for Haplogroup L

Egypt mtDNA and the Nile Valley ኒለ ቫልለይ Dna DiversitY.. The Maternal Hamito-Semitic.. mtDna Haplogroup L

Posted in anthrolpology, Blood type O, Cushitic, DNA, Egypt, Egypt and the Blue Nile, Egypt another Nile Valley Civilization, Egypt MtDNA, Ethiopia, Habeshas, Haplogroup L2 and L3 in West Asia, Indigenous mtDna (mother's) of Egypt, Nile Valley/Nubia, Nilo Saharan, North Africa, O-positive blood, Semitic with tags , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , on April 29, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

Meritaten Tasherit 18th Dynasty

egypts_awakening-mamoud

The mitochondrial DNA (mtDNA) Diversity of 58 individuals from

Upper Egypt, more than half (34 individuals) from Gurna,

Whose population has an Ancient Cultural History, Were studied by sequencing The Control-Region and screening diagnostic RFLP markers.

This Sedentary Population:

(meaning= inhabiting the same location through out life, non nomadic)

Presented similarities to the Ethiopian Population by the

Haplogroups L1 and L2 macrohaplogroup frequency (20.6%), by the

West Eurasian component (defined by Haplogroups H to K and T to X) and Particularly by a High frequency (17.6%) of AfriAsiatic Haplogroup M1.

Mitochondrial DNA sequence diversity from Upper Egypt (Gurna)sedentary population …

As for the maternal (mother’s) inheritance; this is more varied. From a study at Gurna

(of modern Upper Egyptians): Haplogroups;

H 14.7%, I  5.9%, J 5.9%, L0a* 11.1%, L1* 4.9%, L2a1* 20%,

L3* 11.0%, M1  14.9%, N1b  8.8%, T 5.9%, U  8.8%, L2* 2.0%

U4  5.9%, U6 2.9%, L3e* 4.0%, L3b* 1.9%, L1c* 1.0%

L2b* 2.0%. L1b* 4.9%, L3f*6.9%. L3d*1.0%.

Percentages above are based on mtdna frequencies of

Southern Upper Egypt/Nile Valley collectively..

Percentages below are based onmtdna frequency in

Northern Alexandria/Lower Egypt ( Saunier July 2008)..

The Breakdown is predominantly European 67.5% followed by African @ 20.6% and Asian @ 11.9%.

European: R0 and subgroups (31.4%), I (3.2%), J (7.6%), K (4.7%), T (9.4%), U (9.0%), W (0.7%) X (1.4%)

African Haplogroups: L0 (2.2%), L1 (2.5%),  L2 (3.6%) and L3 (12.3%)..

Asiatic Haplogroups: M (6.9%) and N (5.1%)

Results:

The Egyptian Population Data set has a Low Random Match Probability..

The Egyptian Population also shows a Large number of Unique Haplotypes,

Therefore indicating a High mtDna Diversity within the Country

Overall 238 different haplotypes were defined by 228 variable positions.

Of the 238 different Haplotypes, 31 were shared within the database of 277 individuals.

The Haplotype most common in this dataset was observed in five individuals

There were 17 points of Heteroplasmy identified in 15 individuals (5.4% of the database)

At 16 positions: One Sample indicated three positions of point heteroplasmy>

(16519, 73 and 195)…

Other remarks: Egypt is distinctive Bio-geographically, as it is centrally located,

Among three surrounding continents its home Africa, Asia and Europe..

(which group belongs to your mother ? )…..

Of these, The L haplotypes are Nilotic and Indigenous and are typically Supra and sub Saharan..

Haplogroup L2a (mtDNA) has notable frequencies of 22% among the

Hebrew Affiliated Fulani of Nile Valley to Niger to The Gambia

They are at least 70,000-111,100 B.P. The Oldest in Egypt !!

L2a1 also has (49%) MtDna collectively in,

Sudan, Nile- Valley/Nubia, Ethiopia, and Egypt

(from the White Nile to the Blue Nile)..

(the Nile Valley Civilizations)……

Queen Ahmose Nefertari/ New Kingdom 19th Dynasty

L2a is also in the Great Rift Valley regions @

16% Kenya/Sudan and 33% in Mozambique.

Today, the term is most often used to refer to

The Valley of the East African Rift,

The divergent plate boundary which extends from

The Afar Triple Junction southward

Across Eastern Africa, and is in the process of splitting

The African Plate into two new separate plates.

Geologists generally refer to these incipient plates as

The Nubian and Somalian subplates or protoplates.

East African-Asiatic: Plate of Nubia/Somalia and ArabiaAs for haplogroups M1 and U, they are African/Westasian/Eurasian haplotypes, at 30,000 B.P.

Other West-asian/Eur-asian, Haplotypes have been found in 12,000 year old bones in Morocco.

Haplogroups N and I Mtdna are possibly attributable to Arab ancestry, about 15% non-Arab in upper Egypt. But still, most of that would easily be attributable to the Neolithic input from “AsiA” very little of this would be attributable to Arabs.

To sum up, there doesn’t seem to be majority ‘Arab’ genetic component to the Egyptian DNA pool, 20% absolute maximum. A lot of the non African DNA is traceable to the Neolithic farming expansion that swept across North Africa, so it would be a lot lower in reality.

In upper Egypt a maximum of 20% of the Y chromosomes are Non –African.

{MMother’s mtDNA L2a1 has been shown to be prevalent in North Africa }..

{Since the Dynastic times, of Ethiopian-Nubian and Egyptian Kingdoms} …..

Sesostris the Ist 12th Dynasty from Altes Museum inBerlin

So how these people are supposed to have Magically Changed appearance in the past few thousand

years with so little foreign input I’d like to know

Egyptians are Indigenous “African-Egyptian”, Not Euro/Arabs.. They are in essence “African-Arabs”.

They are part African/Asiatics: (Hamito-Semitic) and are members of

The Nile Valley  and the Great Rift Valley , which could be equally known as

The East African Rift , Nile Valley Civilizations…

(“Nile Valley, “North Africa”, “Horn of Africa” and “West Asian Arab Africans”.)

{copy and paste national geographic link on egyptian mummies and dna}

http://news.nationalgeographic.com/news/2008/06/080606-egypt-mummies.html

An important influence on the subsequent genetic landscape

Of the continent is likely to have been the LGM.

Paleovegetational studies have indicated that, between 30,000 and 11,000 years ago,

Much of the continent was extremely arid (Adams and Faure 1997).

The Sahara advanced hundreds of kilometers further south, and the Equatorial Rainforests

Were reduced to a small fraction of their present size, leaving open woodland and savanna in much of the Congo basin.

This may have formed a refuge area from which modern humans later dispersed:

Some with haplogroup L2a East and West, with L1b west;

Perhaps even some with L1a East and L1d Southward.

The origins of these expansions may lie earlier,

At the beginnings of the Later Stone Age, ~40,000 years ago.

Queen Meryt-Amen the 19th Dynasty

The Valley of the Queens, is a place in Egypt where wives of Pharaohs were buried in ancient times. In ancient times, it was known as Ta-Set-Neferu, meaning –‘the place of the Children of the Pharaoh’, because along with the Queens of the 18th, 19th and 20th dynasties (1550–1070 BCE) many princes and princesses were also buried with various members of the nobility. The tombs of these individuals were maintained by mortuary priests who performed daily rituals and provided offerings and prayers for the deceased nobility.

The distributions and ages of L1a, L1c/L3e, and L1d testify to the habitation of East, and Central, and southern Africa, respectively, by modern humans, ~40,000 years ago.

Similarly, L1b, L3b, and L3d imply that West Africa has been inhabited since at least 20,000–30,000 years ago.

Haplogroup L1b is concentrated in West Africa, with some overflow into Central and North Africa

(particularly geographically adjacent areas, connected by the West African coastal pathway)

but little in East, southeastern, or southern Africa.

It is also common in so called African Americans

(~27% of all L1b-types in the database)

By contrast, the commoner haplogroup L3b (fig. 8c) is predominantly West African,

with a substantial representation again in today’s socalled African Americans.

It has also spilled over into North Africa and on into the Near East as well.

And Its sister clade, Haplogroup L3d (fig. 9a), is also mainly West African and African American.

A number of types are found in SouthEastern Africa, including one type (in L3d1), matching a Fulbe/Fulani lineage,

At considerable elevated Frequencies.

L3e (fig. 9b) is the most widespread, frequent, and ancient of the African L3 clades, comprising approximately one-third of all L3 types in sub-Saharan Africa.

This haplogroup has recently been dissected in some detail by Bandelt et al. (2001),

Who suggest an origin for the haplogroup in the Central Africa/Sudan region ~45,000 years ago.

As they recognized, L3e1 in particular is common amongst SouthEastern African Bantu speakers,

Along with some L3e2 and L3e3 lineages.

L3e also represents approximately one-third of all African mtDNA lineages in Brazil.

Alves-Silva et al. (2000)

Finally, there are two small sister clades, L3e3 and L3e4.

L3e3 is primarily West African,But with its root type present at elevated frequency in the

Southeast and with some southeastern African derivatives. There is also a Kenyan/Kikuyu derivative,

Again raising a possible connection with the Eastern stream.

L3e4 is present in East, Central, and West Africa, with One individual in the Southeast,

But is too rare to draw conclusions from.

The area occupied by Cameroon is not always considered as part of the geographic region known as West Africa.

Taking into account its haplogroup composition it could also be considered a genetic outsider.

There are numerous lineages

(L0a, L0a1a, L0a2, L2a1e, L4g, and L5)

that have a more CentralEastern than Western Assignation.

(Pereira et al. 2001Salas et al. 2002Kivisild et al. 2004).

The L4g haplogroupis most frequent in Eastern and

NorthEastern Africa and waspreviously Dated to ~40–45 kya

(Salas et al. 2002Go; Kivisildet al. 2004Go).

Haplogroup L4g (previously designated L3g) is present in both Eastern Tanzanian

Clickspeaking populations at high frequencies (60%Hadza, 48% Sandawe) but is Absent in the SAK.

History of Click-Speaking Populations of Africa Inferred from mtDna …

The only L4 Saudi haplotype belongs to the L4a1 subclade defined by 16207T/C transversion.

Although it has no exact matches its most related types are found in Ethiopia [30].

Four L5 lineages have been found in Saudi Arabia but all have the same

Haplotype that belongs to the L5a1 subclade defined in the

HVSI region by the 1635516362 motif [30]. It has matches in Egypt and Ethiopia.

L6 was found the Most Abundant clade in Yemen [30].

BioMed Central |  Macro-Haplogroup L mtDNA structure in the Arabian Peninsula …

HAPLOGROUP L2A:

Haplogroup L2a is Nilotic and the most common and widely distributed sub- Saharan African Haplogroup and is also frequent in the Americas (~19%).

The wide distribution of L2a in Africa makes identifying geographical origins of lineages difficult.

(Excerpt from: The African Diaspora: Mitochondrial DNA and the Atlantic Slave Trade)

http://www.ncbi.nlm.nih.gov:80/pmc/articles/PMC1182259/

The Main Puzzle is the almost Ubiquitous Haplogroup L2a,

North Africa Tunisian Bay : Golfe de Tunisia Port Saïd { Carthage}Which we suggest may have become”Prevalent “somewhere in

North-Central Africa  { Prehistoric Central North Africa }

Spreading East and West along the Sahel, during the Last Glacial Period or some what earlier..

Example: Modern day Sahel, Tunisia near Libya and Algeria..

Note: The Jerba Islands of Tunisia/Carthage is located in South Eastern Tunisia,

Tunisia, is inhabited by four ethnic groups: Berbers, Arabs, sub-Saharans, and Jews/Hebrews.

(click link below for isolated Sub/Supra Saharan mtdna of jerba/tunisia)

Isolated Haplogroups of Jerba Island Tunisia: L1b, L2a1L2a1c1, L2d2, L3b, L3b1, L3e1a, L3f, M and U

The Island of Jerba/Tunisia is said to be Inhabited First, by the Descendants of  the Mousterian Population

Between the 5th and 6thMillienia B.C. (Tlatli, 1967), Who were later replaced by Berbers of  the Ketama

and Lemata tribes ( Khaldoun 1852).

The First Arab settlement on the Island Occurred in the 7th Century A.D.

Another study shows results also point to a less Ancient western sub-Saharan gene flow to Tunisia, including Haplogroups L2a and L3b.

This conclusion points to an Ancient African gene flow to Tunisia before 20,000 BP.

These findings parallel the more recent findings of both archaeology and linguistics on the prehistory of Africa.

The present work suggests that sub-Saharan contributions to North Africa have experienced several complex population processes after the occupation of the region by anatomically modern humans.

Our results reveal that Berber speakers have a foundational biogeographic root in Africa and that deep African lineages have continued to evolve in  supra-Saharan Africa.

All Ethiopian {L2} lineages can be seen as derived from the two subclades { L2a1 and L2b }

(click link for Ethiopian/Yemenis Haplogroup mtDNA BreakDown): > articlerender.fcgi

Most Ethiopian L2a1 sequences share mutations at nps {16189 and “16309″}

However, whereas the Majority (26 out of 33) “African Americans” share Haplogroup {L2a}

complete sequences could be partitioned into four subclades by substitutions at nps

Coding Regions and Haplogroups from Full Genome Sequence TEST:

1. L2a1e-3495 has (USA Origins)

2. L2a1a-3918 has (KENYA) and (USA Origins)

3. L2a1f-5581 has (SOUTH AFRICA),(BURKINA FASO), (OMAN), (DOMINICAN- REPUBLIC), and (USA) Origins

4. L2a1i-15229 has (GUINEA-BISSAU), (WEST AFRICAN), and (USA) Origins.

None of those sequences, (shown above) were observed in our Ethiopian {“16309″} L2a1 samples.

EXCERPT FROM GENETIC STUDY 2012.

“Reconstructing Ancient L Mitochondrial DNA links between Africa and Europe”

Mar ́ıa Cerezo,1,7 Alessandro Achilli,2 Anna Olivieri,3 Ugo A. Perego,3,4
Alberto Go ́mez-Carballa,1 Francesca Brisighelli,1,5 Hovirag Lancioni,2
Scott R. Woodward,4 Manuel Lo ́pez-Soto,6 A ́ngel Carracedo,1 Cristian Capelli,5 Antonio Torroni,3 and Antonio Salas1,7,8

A large proportion (65%) of the African-European mtDNAs investigated could be attributed to modern and well-documented demographic routes that existed during the Romanization period, the Arab conquest, and the trans-Atlantic slave trade. However, there is strong evidence pointing to the fact that the remaining 35% of the African L-European mtDNAs stand as modern witnesses of sporadic population movements occurring between the two continents that might have begun as early as 11,000 yr ago (Fig. 5).

These contacts were not only restricted to North Africa, but connected Sub- Saharan regions to Europe directly via coastal routes or first crossing North African territories toward the Mediterranean Sea. 10,000 Years before Slavery, Arab Conquest or Roman period Outside of Africa.

Attention should also be brought to the L2a1 clads above who also have an Indigenous North American Origin i.e.. (Indigenous Native American) (USA Origins), although they carry an African Haplogroup. Some of these Haplogroups are only found in Europe or the Americas, and Not in Africa. These groups may also produce a Mulatto, Native American, or European Pheno-type (features such as Straight or Curly hair types and multitude of different complexions). Some of these particular Haplotypes has African and American Origins, but the Haplogroup is 100% African. (i.e.. North African, East African, South African, West African). This group may also share genetic ancestry with other Indigenous Americans, as well as the Asiatic-African Moors of America.

A single L2d1 sequence from the Yemeni sample shares the haplotype that has so far been observed in Sudan and in southeastern Africa

Ethiopian L2b sequences form a subset of a predominantly West African clade, distinguished from West African lineages by a transition @ np“16145″.

(Dr. Salas et al.) click link for Ethiopians/Yemenis (Horn of Africa) Gate of Tears mtdna study> (2002)….

PCR AMPLIFICATIONS:

PCR amplification of (a) 27 selected NumtS in 4 healthy subjects from

Different ethnic groups ex..  L2a1-c1/16086C in (North Africa) Figure 2

Costa‘s link to mtDna diversity of Tunisia

Ancient Local Evolution of African mtDNA Haplogroups in Tunisian …

BioMed Central | Full text | The RHNumtS compilation:  North Africa L2a1c1…

Mitochondrial DNA Heterogeneity in Tunisian Berbers.pdf

Tunisia’s reproductive mtDna groups Isolates on Jerba Island.pdf

RootsWeb: GENEALOGY-DNA-L [DNA] mtDNA sequences from Tunisian …

http://www.ncbi.nlm.nih.gov/pubmed/Tunisia and Morrocan Haplogroup L

mtDNA Haplogroup L 72.5% diversity in Sudan (East Africa)

Mitochondrial DNA  L2a and L3a Variation in Mauritania and Mali

RootsWeb: GENEALOGY-DNA-L [DNA] New Egyptian mtDNA sequences

European Journal of Human Genetics – Table 1 for article: The Canary Islands and North Central/NW Africa…

Haplogroup L2a has frequencies of 14% among Algerian Arab/Berbers and

10% among Bilād al-Sūs Morrocan Arab/Berbers in

The Sousse Valley North Africa..

We recognize, however, that the origins of these haplogroups may be more ancient than we can trace

(L2, for example, may be well >70,000 years old )….. and that, in such cases,

evidence of the earlier distribution of these clusters may have been erased by subsequent demographic processe.

We have attempted partly to disentangle the structure of L2a, retaining as irreducible on present evidence three major squares close to the root of the cluster. These reticulations link eight main clusters by single-step mutations.

We assume that the main reticulations of the network are due to the existence of rapid transitions at positions 16189 and 16192

(Howell et al. 2000), which approach saturation due to the high time depth of African lineages.

We also assume that position 16309 is more stable than the two known fast sites and therefore is not responsible for the main reticulations.

On these grounds, clusters α1-α2-α3, as well as β1-β2-β3, might be collapsed into two main clusters,

One of them with the basal motif of “(L2a)” and the other harboring the transition at “16309″ (L2a1).

Several instances in which 16309 must nevertheless evolve in parallel can then be read off the network..

Full report link below on genetic mtdna migrations:

Haplogroup L2a can be further divided into L2a1, harboring the transition at 16309 (Salas et al. 2002).

The most extensive pan-African haplotype

(16189 16192 16223 16278 16294 16309 16390) is in the L2a1 haplogroup.

This sequence is also observed in West Africa among the Malinke, Wolof, and others; in

North Africa among the Maure, Hausa, Fulbe, Tuaregs , Hebrews and others; in

Central Africa among the Bamileke, Fali, and others; in South Africa among the

Khoisan family including the Khwe and Bantu speakers; and in

East Africa among the Kenyan/KikuyuClosely related variants are observed among

The Tuareg in North and West Africa and among the

East African Dinka of Sudan and Eastern Somalians. (Ely et. al. 2006; Watson et al. 1997).

Also striking is the presence in Sakai, Mani of  Thailand of an unequivocal representative

With this  motif (16223–16274–16278–16294– 16309)

Of the sub-Supra Saharan African L2a haplogroup (Torroni et al. 2001),

Which again is compatible with the physical characteristics of this Negrito group.

Although the suggestion that the first spreading out of Africa of modern humans could have carried

some L2 lineages in addition to the L3 ancestors (Watson et al. 1997)…

(Note: my thoughts are the Sakai, and  Mani people of Thailand who genetically belong to the

Motif: 16223–16274–16278–16294– 16309 could very well belong to L2a1 by 16309 as according to the updated

Haplogroup Phylotree 2010 by Van Mannis) ex: Coding region 12693, 15784, and HVS1: (16309) for L2a1.

A compliation 0f 185 mtDNAs sampled across North Africa showed that about Half of the

Lineages belonged to the L Haplogroups otherwised observed mainly in Sub-Saharan Africa

And  that most of the rest fell into Haplogroup U6 (Sala et al. 2002) Which perhaps Originated

In the Near East and Spread into North Africa ~30 thousand years (KY) ago (KYA) (Maca-Meyer et. al. 2003).

A proportion of 1/4 to 1/2 of North African female pool is made of typical sub-Saharan lineages, in higher frequencies as geographic proximity to sub-Saharan Africa increases.

The distribution of the main L haplogroups in North Africa somewhat reflects the known trans-Saharan slave routes:

West is dominated by L1b, L2b, L2c, L2d, L3b and L3d;

the Center by L3e and some L3f and L3w;

the East by L0a, L3h, L3i, L3x and, in common with the Center, L3f and L3w;

while, the ubiquitous Haplogroup L2a is almost everywhere.

Another major contribution to the pool of North Afri- can populations was the sub-Saharan one.

It is known that a proportion of 1/4 to 1/2 of North African female pool is made of typical sub-Saharan lineages

(designated as haplogroups L0-L6)

Japan mtDna Genome Variation in  Sakai Eastern Asia from Thailand…

Joshua Project – Sakai, Mani of Thailand Ethnic People

The mtDna of the  trans-Saharan slave trade

HAPLOGROUP L2a

mtDNA phylo tree Build 10 (10 Aug 2010)

PhyloTree.org | sub-haplogroup |Haplogroup L

The Making of the African mtDNA Landscape

Mitotool.org Macro-Haplogroup L  PhyloTree and Ethnic Groups..

Comparison of Craniofacial features of African-Asiatic Human Groups.

Evidence of the Early Penetration of socalled Negroes in  Prehistoric Egypt”

Click link for Origin Date of mtDna>{TB5}

L1b 30,550 (16,250) B.P.
L2a 55,150 (19,350) B.P.
L2a1 33,700 (13,400) B.P.
L2d 121,900 (34,200) B.P.
L3e 49,250 (11,750) B.P.
L3e1a 26,750 (12,000) B.P.
L3e1 32,150 (11,450) B.P.
L3b 21,600 (6,850)  B.P.
L1c2 44,100 (10,650) B.P.
L3d 30,250 (8,450) B.P.
L3f 36,300 (12,800) B.P.

University College London 2004. mtdna study..

nile-valley-in-egypt

Afterword:

According to the profile of West African Dna study, on

Nilotic – Haplogroup L2a

The Percentages clearly shows an clear Eastern Distribution:

Eastern Africa 82%,

Western African 69%,

North-West African 27%,

South Africans 3% Kung Khwe

As well as Cabo Verde Islands 20% and

Fulani people from East-West, Central and North Africa at 22%

Chart on pg.5 (click counter clock-wise to view)

Shows Sahara, Horn of Africa and Congo regions as Well as Krings 1999. Nile Valley mtdna% ....

Click Link below:

http://www.africandna.com/ScienPapers/MtDNA_Profile_of_West_African_Guineans.pdf

Egyptian Triad Statue. Menkaura The Goddess Hathor and Goddess BatNorth Africans tend to cluster with West Africans, suggesting that the sub-Saharan component of

North Africans Originates primarily from West rather than East Africa

(as expected, on geographical grounds).

Unlike other North Africans,Egyptians are closer to East Africans

than to West Africans. [Rando et al. 1999].)

PC2 has a large contribution from the Eastern lineage groups L3g and L3*;

However L2a, L1b1a, and L3e2* also make a similar contribution.

And though Egypt in the North as well, Egyptians tend to Genetically cluster with East Africans

mtDna Lineages of  Ethiopians, Egyptians and Hebrew Yemenis, Populations MDS plot (fig.3)

Clustered together with the Egyptian Population

In between the Near Eastern and West African as well as Southern African Clusters.

It is interesting that both Semitic and Cushitic Speaking Populations of Ethiopia,

Were close to each other and did not reveal significant differences

http://www.ncbi.nlm.nih.gov:80/pmc/articles/PMC1182106/

A recent study on mtDNA suggested that modern Nubians and Egyptians are much more similar to one another than either is to southern Sudanese populations and that the divergence between the two northern populations may have occurred during the past few hundred or few thousand years (Krings et al. 1999).

Forensic Misclassification of Ancient Nubia:

http://www.cas.gsu.edu/anthropology/images/ANTH/Forensic_Misclassification_PDF.pdf

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NOTE: Haplgroup L2a being prevalent in North-Central Africa with an  Origin Date of 55,150 B.P.

Would place L2a in the Upper Paleolithic era in North Africa beginning around 50,000 years before the present (ybp),

As well as the Mousterian Pluvial period circa 50,000 B.C. and  lasting 20,000 years, and finally ending around 30,000 ybp.

Archaeologist Richard G. Klein, argues that almost everywhere, whether Asia or Africa or Europe, before 50,000 years ago

All the stone tools are very much alike and Unsophisticated.

However after 50,000 years ago there is “Sharp Increase” in the diversity of Artifacts.

For the First Time Bone Artifacts, and the First Art appear in the fossil record in Africa.

The First Evidence of Human Fishing is also noted from Artifacts in places like Blombos cave in South Africa.

After 50,000 years ago, Firstly in Africa, it was found that Human Artifacts could be placed into Many different categories,

such as {Projectile Points, Engraving Tools, Knife Blades, and Drilling and Piercing Tools}

All of the above are Found in (Al’kebu-lan) AFRICA...

Frequencies of  North West- East Asiatic Africans

(Haplogroup L, mtdna % chart)

Origin Population Number tested %
East Africa Somalia 26 Watson et al. (1997) 50.00%
East Africa Sudan 112 Afonso et al. (2008) 72.50%
East Africa Ethiopia 270 Kivisild et al. (2004) 52.20%
North Africa Libya (Jews) 83 Behar et al. (2008) 3.60%
North Africa Tunisia (Jews) 37 Behar et al. (2008) 2.20%
North Africa Morocco (Jews) 149 Behar et al. (2008) 1.34%
North Africa Tunisia 64 Turchi et al. (2009) 48.40%
North Africa Tunisia (Takrouna) 33 Frigi et al. (2006) 3.03%
North Africa Tunisia (Zriba) 50 Turchi et al. (2009) 8.00%
North Africa Morocco 56 Turchi et al. (2009) 26.80%
North Africa Morocco (Berbers) 64 Turchi et al. (2009) 3.20%
North Africa Algeria (Mozabites) 85 Turchi et al. (2009) 12.90%
North Africa Algeria 47 Turchi et al. (2009) 20.70%
Europe Italy (Latium) 138 Achilli et al. (2007) 2.90%
Europe Italy (Volterra) 114 Achilli et al. (2007) 2.60%
Europe Italy (Basilicata) 92 Ottoni et al. (2009) 2.20%
Europe Italy (Sicily) 154 Ottoni et al. (2009) 2.00%
Europe Spain 312 Alvarez et al. (2007) 2.90%
Europe Spain (Galicia) 92 Pereira et al. (2005) 3.30%
Europe Spain (North East) 118 Pereira et al. (2005) 2.54%
Europe Spain (Priego de Cordoba) 108 Casas et al. (2006) 8.30%
Europe Spain (Zamora) 214 Alvarez et al. (2010) 4.70%
Europe South Iberia 310 Casas et al. (2006) 7.40%
Europe Spain (Canaries) 300 Brehm et al. (2003) 6.60%
Europe Spain (Balearic Islands) 231 Picornell et al. (2005) 2.20%
Europe Portugal 594 Achilli et al. (2007) 6.90%
Europe Portugal 549 Pereira et al. (2005) 5.83%
Europe Portugal (North) 187 Pereira et al. (2005) 3.21%
Europe Portugal (Central) 239 Pereira et al. (2005) 5.02%
Europe Portugal (South) 123 Pereira et al. (2005) 11.38%
Europe Portugal (Madeira) 155 Brehm et al. (2003) 12.90%
Europe Portugal (Açores) 179 Brehm et al. (2003) 3.40%
Middle East Yemen 115 Kivisild et al. (2004) 45.70%
Middle East Yemen (Jews) 119 Behar et al. (2008) 16.81%
Middle East Bedouins (Israel) 58 Behar et al. (2008) 15.50%
Middle East Palestinians (Israel) 117 Achilli et al. (2007) 13.68%
Middle East Jordania 494 Achilli et al. (2007) 12.50%
Middle East Iraq 116 Achilli et al. (2007) 9.48%
Middle East Syria 328 Achilli et al. (2007) 9.15%
Middle East Saudi Arabia 120 Abu-Amero et al. (2007) 6.66%
Middle East Lebanon 176 Achilli et al. (2007) 2.84%
Middle East Druzes (Israel) 77 Behar et al. (2008) 2.60%
Middle East Kurds 82 Achilli et al. (2007) 2.44%
Middle East Turkey 340 Achilli et al. (2007) 1.76%
South America Colombia (Antioquia) 113 Bedoya et al. (2006) 8.00%
South America Mexico (North-Central) 223 Green et al. (2000) 4.50%
South America Argentina 246 Corach et al. (2009) 2.03%

Funerary Boat from Egypt Middle Kingdom 12th Dynasty

Mitochondrial control region sequences from an Egyptian population …

Mtdna Diversity in a Sedentary Population from Egypt.

National Geographic Magazine -Ancient Egyptian Origins .

Ancient Egyptian Origins

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The Saga of Sepharda ሰፕሃርዳ .. by Debra Katz

Posted in African mtdna in Europeans, Asiatic African mtdna in Europeans, Egypt MtDNA, Ethiopia, Europeans wit African mtDna, Indigenous people, L2a1, Levant, Saga of Sepharda, Semetic People, Semitic, Sephardic Hebrews, Sephardic Jews with tags , , , , , , , , , , , , , , , , , , , , , , , , , on April 27, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

Sephardic-Hebrew Tombstone

THE SAGA OF SEPHARDA

by Debra Katz

Working Theory in Progress  of
 How Ashkenazi and Sephardic Jews, Blacks and  Whites  the “Caribbean”, 
 Roma Gypsies, and

African Americans all Sprung from the Same Well !

~180,000 years ago

A woman [womb-man]  walked through Olduvai Gorge

(in present day East Africa Tanzania)

with her small tribe of fellow Homo Sapiens. Her people were destined to be the only species of hominids that would survive, but right now they’re not the only “people” by far…Neanderthals and Homo Erectus still dominate most of the planet.  But this lady is special because of all the women walking with her, she alone will be the direct maternal line ancestor of every person alive on the planet today.  You may have read about her…“Mitochondrial Eve” and her haplogroup designation is “L”.

~75,000 years ago

In the heart of Central Africa a baby girl is born into Eve’s tribe …she is just like her mom, except that one letter in her mtDNA mutated.

She didn’t know it, but she was the beginning of a new haplogroup branch—L2—that would become the most common haplogroup in Africa.  About this time a small band from another branch of “mtDNA mutants”L3—decided to seek better weather and food by bravely crossing the Gate of Tears off the horn of Africa. They entered the Arabian peninsula—-and from there, this band of 200 or less people would go on to populate the rest of the World.

But their story is not ours…for the L2 baby girl and her descendants all stay in Africa.

~ 55,000 years ago

Among an L2 tribe living in West/Central Africa, another baby girl is born with a new mtDNA mutation…making her the start of a new haplogroup branch L2a.

Her descendant daughters remain without much mtDNA change for over 50,000 years!

Over that time, some of her people start to migrate across Central Africa to the East area now called EThiOpiA.

Others of her people started heading North along the nile coast, settling in North Africa and EgYpt and even reached the Levant

(now Israel, Syria, Jordan, Turkey).

~2,500 years ago (500 BCE)

Somewhere in North Africa, EgYpt or the Levant, a baby girl is born with yet another mtDNA mutation…starting the haplogroup line known as L2a1.

Some of her tribes people intermarry with the newly forming Hebrew tribes in the Levant and become Hebrews/Jews.

~ 2,200 years ago  (~200 BCE)

It is among this group of African Jews that our common ancestress was born!  For fun I’m going to call her Sepharda Fulanivich—a name that hints at our group’s main strains.

Sepharda had no special mutation that would create a new haplogroup,

but she was unique in the way we are all unique…and special because all our maternal lines would lead back to her.

Given how many of us have similar eye color, Sepharda may well have had green/blue eyes. This trait would have been recessive in her daughter descendants, dominated by their brown-eyed mates.

but always ready to appear again if and when a blue-eyed spouse came along.

~1900 years ago (~100 CE)

One of Sepharda’s descendant daughters was part of a group of Jews who fled the Roman invasions of Judea and headed back into North Africa. They formed a tribe that came to be known as the Fulani.

As they migrated across North Africa, they first settled in the Morocco/Mauritania area and over the next few centuries slowly spread throughout West Africa, converting to Islam, but retaining both the appearance and some traditional memories of their Hebrew origin in the Levant. (Their DNA held the memory as well.)

At about this very same time—give or take 100 years or so!—another of Sepharda’s descendant daughters also fled Judea, heading with her family to Spain (Sepharad, in Hebrew).  They may have gone up through Italy first or directly to Spain…we can’t know as yet.

But one way or another, they became Sephardic Jews.

~600 years ago (~1400 CE)

For many centuries, Spain was a place where Jews/hebrews flourished, but things started deteriorating after the Moors left and the Pope’s intolerant minions came to power. Many Jews left the country, heading for France and then Bavaria (Germany), where they mingled with the Ashkenazi Jewish populations already living there.

One of Sepharda’s descendants was among them and she is the common ancestor of all the

Ashkenazi Jewsin our groupthe set of 13 families who match HVR1&2 exactly.

More on their story in a couple of centuries…(-:)

~300 years ago (~1700 CE)

This was a lousy time period for almost all of Sepharda’s descendants.

First we go back to West Africa and find that some of her Fulani daughters are among the ones being captured by the British and sent to the Caribbean and the new colonies in America. 

Indeed, because we know most of these enslaved daughters of Sepharda were sent to North Carolina originally, we can predict that their common ancestress lived when the trade to that area was peaking—1720 to 1760.

These daughters are the ancestors of almost all of our African-American matches.

Then, over in Spain, things had gone from bad to worse, with a complete expulsion of Jews in 1492.  As noted above, some fled into Europe.  Many more went farther south into the Turkish (Ottoman) Empire and North Africa. However—-drum roll—a fair number headed for the

British West Indies and by ~1650 CE there was a whole bunch of Sephardic Jews settled in Jamaica and the Bahamas.  In 1691 another “auto de fe” (more “burning of Jews”) in Toledo Spain sent another wave of Spanish Jews to Jamaica.

Many of these Jews came as “singles” and ended up intermarrying with the population from the British Isles that had settled there.  And among those migrating Spanish women were Sepharda’s daughters, many of whom married non-Jewish Brits and lost the memory of their Jewish past.

Their lines led to our West Indies matches.

And I believe it also explains some “not-Jewish white” folks who trace themselves back to the 17th century in Rhode Island and New Jersey

By ironic coincidence, Jamaica was also a drop for slave traders and it looks very possible that some of our Jamaican matches are from the African slave branch of our line rather than the Sephardic Jewish branch!

~250-400 years ago (1600-1750 CE)

Getting back to those Ashkenazi Jews, we can spell out their story a little more.

Some stayed in Germany …but as the centuries passed and German anti-Semitism increased, other descendant daughters started moving east into Poland and then south towards Romania (where the ancestors of some of us joined up with other Jewish Romas (gypsies)…

interestingly, a very recent study found what was to them a startling level of “L2a” haplotypes among Roma gypsies in Slovakia!

About 1700 or so, some of the Polish daughters migrated north, where some lines settled in Belarus and others went up farther into Lithuania and Latvia .


Afterword

Back in West Africa, right now, some of Sepharda’s daughters are living and don’t even realize all of us cousins elsewhere in the world are thinking of them. That is also true no doubt in Spain…and all the other places our lines have passed through. Some women moved on, but not all of them.

And imagine if Sepharda could come back to life and meet each of us and realize that without her existence….none of us would be here.

That’s the power of one.

Updated October 2008

Sephardic Tombstones 2

Author’s Note: This working theory will soon be greatly enhanced by new information as nine of the descendants above (including slave descendants and Caribbeans) get their currently pending Full Genome Sequence results…

Sephardic Jews cutting stones in Jerusalem - Kurdish Jews.

Sephardic Jews cutting stones in Jerusalem – Kurdish Jews.

Updated info on L2a1 Saga of Sepharda  by Debra Katz on link below:

http://www.billipilli.com/sepharda/  (SOURCE  FOUND  ONLINE >

The Matrilineal Ancestry of Ashkenazi Jewry:

Portrait of a Recent Founder Event

{Doron M. Behar1, Ene Metspalu2, Toomas Kivisild2,}

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Phylogenesis of African mitochondrial DNA lineages in European Slavs (slavic people).

Posted in A-positive blood, AB-Postive blood, African mtdna in Europeans, anthrolpology, Ashkenazi Hebrews L2a1, Asia and Europe.., Asiatic African, Asiatic African mtdna in Europeans, B-postive blood, Euro-Asiatic African, Europeans wit African mtDna, O-positive blood, Sephardic Hebrews, Sephardic Jews with tags , , , , , , , , , , , on April 27, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

In the present study,

we completely sequenced eight African haplotypes of mtDNAs revealed previously in 2018 individuals from Slavonic populations of Eastern and Central Europe by means of mtDNA control region sequencing and coding region RFLP analysis (Table 1).

All individuals with African variants of mtDNA identified themselves as ethnical Slavs (ie ‘indigenous’ Russians, Slovaks, Czechs or Poles) and were unaware of their African Ancestry until Molecular Genetic Studies.

Figure and tables index

Whole mitochondrial genomes were amplified and sequenced by means of the procedures described in Torroni et al.21 Sequencing reactions were run on Applied Biosystems 3130 Genetic Analyzer.

Sequences were edited and aligned by SeqScape v. 2.5 software (Applied Biosystems, Foster City, CA, USA), and mutations were scored relative to the rCRS.20 The eight complete mtDNA sequences have been submitted to GenBank (accession numbers EU200759–66).

For comparative purposes, a large number of published African and Eurasian mtDNA HVS I sequences and any available HVS II or RFLP data were used (see references1, 18, 19, 22, 23). In addition, complete or nearly complete mtDNA sequences pooled in MitoMap mtDNA tree24 were taken into analysis.

The complete mtDNA tree was reconstructed manually and verified by using median-joining algorithm with NETWORK 4.1.0.9.25

For phylogeny construction, the length variation in the poly-C stretches at nts 16180–16193 and 309315 were not used.

Haplogroup divergence estimates ρ and their standard errors were calculated as average number of substitutions in the mtDNA coding region from the ancestral sequence type.26, 27

To estimate the time to (tmrca) the most recent common ancestor of each cluster,

The evolutionary rate corresponding to 5140 years per substitution in the coding region was used.28

Haplogroup L1b lineage detected in Russian individual is characterized by the transition at position 16175 that is a

Marker of ‘Europeanspecific’ L1b-subcluster revealed also in Germany and medieval Spain (Table 1).

Comparison of its complete genome sequence with the data presented in MitoMap mtDNA tree24shows that

Russian sample belongs to L1b1a subcluster defined by mutations at positions 2768 and 5393 (Figure 1).

This subcluster is widespread in Africa being found in 22 individuals presented in MitoMap mtDNA tree.

A coalescence time estimate of subcluster L1b1a

(calculated from the average sequence divergence and its standard error according to Sailard et al27)

Corresponds to 8943±1400 years, suggesting a relatively recent (post-Neolithic or later) arrival of the L1b1a lineage into Europe.

Note, that it is only the approximate lower time boundary of the actual arrival of this mtDNA lineage.

Haplogroup L2a samples were found in three individuals, two of whom are Slovaks and one comes from the Czech Republic.

It is noteworthy that among them there is L2a branch defined by mutation at 16218 that is absent in published HVS I L2a data from Africa and Eurasia (Table 1).

Complete Genome Sequencing demonstrates that these two individuals are characterized by two coding region mutations

(at positions 6722 and 12903) and

Represent a branch that is absent among 50 individuals from the L2a macro haplo family collected together in

MitoMap mtDNA tree  (Figure 1).

A coalescence time of this branch is estimated as 10, 280±5140 years, though inferred only from two complete genomes.

Slovak L2a1 Haplotype characterized by transition at 16051 also seems to be very scarce.

This control region sequence type has been recently detected in different parts of Eurasia only twice – in France31 and in Eastern Iran.32

Based on coding region variation data and comparison with MitoMap tree,

This Haplotype L2a1c belongs to a specific subcluster defined by mutations at HVII positions 3010 and 6663.

Aforementioned subcluster seems to be ancient, with an estimated coalescence time of 24 ,672±3561 years for 10 mtDNA genomes analyzed.

Therefore, the present data do not allow us to infer exactly when the African mtDNA lineages were introduced into Gene Pool of

Eastern EuropeansBoth Prehistoric and more Recent gene flows...

(for instance, such as the potential Jewish L2a1 contribution42)

Might have led to African mtDNA admixture into Slavonic gene pools.

AFTERWORD:

All individuals with African variants of mtDNA identified themselves as Ethnical Slavs

(ie ‘indigenous’ Russians, Slovaks, Czechs or Poles)

and were totally unaware of their

African Ancestry until molecular Genetic Studies.

Population (sample ID) HG HVS I sequence HVS II sequence Frequency and references
Russians (Tu_67) L1b 126 175 189 223 264 270 278 311 400 73 182 185GT 195 247 263 315iC 357 1/68311, 12, 13
Slovaks (Slv_222) L2a1 172 189 192 218 223 278 294 309 390 73 143 146 152 195 263 309iC 315iC 1/20716
Czechs (Cz_2972) L2a1 189 218 223 247 278 294 309 390 73 143 152 195 263 309iC 315iC 1/27915
Slovaks (Slv_191) L2a1 51 223 278 294 309 390 73 143 146 152 195 263 309iC 315iC 1/20716
Russians (Ka_69) L3b 124 223 278 294 362 59 73 152 217 263 315iC 1/68311, 12, 13
Poles (Pl_B_69) L3d 124 223 73 151 152 195 263 315iC 1/84912, 13
Russians (Vo_6) M1 129 182AC 183AC 189 249 311 73 195 263 309iC 315iC 2/68311, 12, 13
Russians (Vl_78) M1 183AC 189 249 311 73 195 263 315iC 1/68311, 12, 13

PhyloTree.org | tree | L

African admixture in Europe – Wikipedia, the free encyclopedia

Full figure and legend chart of African mtdna is Euro Slavic people(71K)

European Journal of Human Genetics – Reconstructing the phylogeny mtDNA report.doc …

Table 1 Chart- mtDNA control region seq. of  African-specific haplogroups detected in Slavs .


Macro-Haplogroup L Family in “Yemen የመን / Oman ኦማን” Sabaeans, Habeshas of South West Asia.”

Posted in Afro Arabs, afro asiatic, anthrolpology, DNA, Haplogroup L2 and L3 in West Asia, Haplogroups L4, L2a1, L5, L6, L7, Oman mtDna, Saudi Arabia mtDna, Yemen mtDna with tags , , , , , , , , , , , , , on April 27, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

dark-colored-yemenis

Haplogroups L1,L2,L3A in the Near East reach their highest frequency in the Yemen Hadramawt (~35%).

Other Arab populations—Palestinians, Jordanians, Syrians, Iraqis, and Bedouin—have ~10%–15% of lineages of

sub-Saharan African Origin. These types are rarely shared between different Arab populations.

By contrast, non-Arab Near Eastern populations—Turks, Kurds, Armenians, Azeris, and Georgians—have few or no such lineages, suggesting that gene flow from Africa has been specifically into Arab populations.

For comparison, southern European mtDNAs include only ~2% of these lineages, and northern Europeans <1% (Richards et al.2000).

The only European Region to stand out is Iberia, where ~4% of mtDNAs belong to these clusters, probably a trace of the

Medieval Moorish conquests

(Côrte-Real et al. 1996; Richards et al. 2000).

The most extensive pan-African haplotype (16189 16192 16223 16278 16294 16309 16390) is in the L2a1 haplogroup.

This sequence is observed in West Africa among the MalinkeWolof, and others; in North Africa among the Maure/Moor

Tuareg in North Africa and West Africa and among the East African Dinka and Somali.

(Ely et. al. 2006; Watson et al. 1997)Moors – Wikipedia, the free encyclopedia

The African Maure

Mauritania – Maures

HAPLOGROUP L2a

L2

There is also evidence from one sample (Semino et al. 1989) that in parts of Sicily, which was held by the Arabs between 8251091 a.d.

Haplogroup L1 and Haplogroup L2 amount to ~4%.

young-yemenis-boy Macro-Haplogroup L Familia

In

The Arabian Peninsula

Sub-Saharan Africa L lineages in Saudi Arabia account for 10% of the total. χ2 analyses showed that there is not significant regional differentiation in this Country. However, there is significant heterogeneity (p < 0.001) when all the Arabian Peninsula countries are compared. This is mainly due to the comparatively high frequency of sub-Saharan lineages in Yemen (38%) compared to Oman-Qatar (16%) and to Saudi Arabia-UAE (10%). Most probably, the higher frequencies shown in southern countries reflect their greater proximity to Africa, separated only by the Bab’al Mandab strait.Yemenis with Ak47 and Knife

However, when attending to the relative contribution of the different L haplogroups,

Qatar, Saudi Arabia and Yemen are highly similar for their L2 (36%), L3 (34%) and L0 (21%) frequencies whereas in

Oman and UAE the bulk of L lineages belongs to L3 (72%). In this enlarged sample of Saudi Arabs,

Representatives of all the recently defined East African haplogroups L4 , L5 , L6 and L7 , have been found.

The only L4 Saudi haplotype belongs to the L4a1 subclade defined by  (16207) T/C transversion. Although it has no exact matches its most related types are found in Ethiopia.

Four L5 lineages have been found in Saudi Arabia all have the same haplotype that belongs to L5a1 defined in the HVSI region by (16355 – 16362) motif.

It has matches in Egypt and Ethiopia. L6 was found the most abundant clade in Yemen . It has been now detected in Saudi Arabia but only once.

This Haplotype (16048-16223*-16224-16243-16278*16311) differs from all the previous L6 lineages by the presence of mutation (16243).

In addition it lacks the (16362) transition that is carried by all L6 lineages from Yemen but has the ancestral (16048) mutation only absent in one Yemeni lineage.

This Saudi type adds L6 variability to Arabia, because until now L6 was only represented by a very abundant and a rare haplotype in Yemen.

Attending to the most probable geographic origin of the sub-Saharan Africa lineages in Saudi Arabia, 33 (61%) have matches with East Africa, 7 (13%) with Central/West Africa whereas the rest 14 (26%) have not yet been found in Africa.

Some of them belong to haplogroups with Western Africa origin and the other half to Haplogroups with Eastern Africa adscription. It is also notable frequencies of Haplogroup L lineages reached the area as consequence of slave trade, but more ancient historic contacts with NorthEast Africa are also well documented.

The mtdna Of the Haplogroup L family remains indigenous in these Regions. (ex. 15o,000 b.p. to 70,ooo b.p. hap-grps Lo-L4)Yemins Elder with Afro Young Brothers

We compared the frequency of Haplogroups L1, L2, L3A in

Jewish Communities from the Near East with that in non-Jewish communities residing historically in the same area (table 1).

Near Eastern Jewish groups have smaller frequency of mtdna % in

Haplogroups L1, L2, L3A

(as, indeed, do Ashkenazi Jews [Thomas et al. 2002]).

The only exception is in Jews from Yemen, but, even here, these lineages amount only to a quarter of their frequency in the non-Jewish sample from the Hadramawt.

It is conceivable that Haplogroups L1, L2, L3A have been lost from the Jewish communities as a result of Genetic Drift

Although the independent loss of both L1 and L2 from all Jewish groups seems unlikely.

{However, L2a1a, as defined by a substitution at (np 16286)

(Salas et al. 2002), is now supported by a

Coding-region marker (np 3918) (fig. 2A) and was found in four of six Yemeni L2a1 lineages.

L2a1a occurs at its highest frequency in SouthEastern Africa

(Pereira et al. 2001; Salas et al. 2002).

Both the frequent founder haplotype and derived lineages

(with 16092 mutation) found among

Yemenis have exact matches within Mozambique sequences

(Pereira et al. 2001; Salas et al. 2002).

Most Ethiopian L2a1 sequences share mutations at nps 16189 and 16309 (L2aβ2 [Salas et al.2002]),

and a minor portion, L2a1c, shares mutations at nps 16209, 16301, and 16354

(within cluster L2a α1 [Salas et al. 2002]).

The L2a1β2 HVS-I motif shows a pan-African spread (Salas et al. 2002).

Whereas the majority (26/33) of African American L2a complete sequences could be

partitioned into four subclades by substitutions at nps 3495, 3918, 5581, and 15229

(Torroni et al. 2001; Howell et al.2004),

None of these were observed in our Ethiopian L2a1 samples.

A single L2d1 sequence from the Yemeni sample shares the haplotype that has so far been

Observed in Sudan and in SouthEastern Africa (Salas et al. 2002).

Consistent with figure 7a of Salas et al. (2002),

Ethiopian L2b sequences form a subset of a predominantly West African clade,

Distinguished from West African lineages by a transition at np 16145.}

Several other lines of evidence also support recent Introgression – Hybridization

mtDNA lineages among Ethiopian, Egyptian, and Yemeni populations,

the MDS plot (fig. 3clustered them, together with Egyptians, in between

the Near Eastern and the West African and Southern African clusters

Consistent with that, the admixture analysis showed the Yemeni population as a

Hybrid of Predominantly Ethiopian and Near Eastern maternal Gene pools,

which provides no significant support for gene flow from Mozambique (table 2).

NOTE: Haplogroup L2a1 was found in 5 European Ashkenazi Jewish countries {Doron M. Behar1, Ene Metspalu2, Toomas Kivisild2,}

More than half of the Yemen L1, L2, L3A lineages occur at the tips of the mtDNA tree (cf. Salas et al. 2002),

Indicating that they have been generated by mutation relatively recently.

Furthermore, a majority of the L1, L2, L3A lineages in the Hadramawt—such as members of L2b, L2d, L3b, and L3d—trace back ultimately to West Africa,

So that it is likely that they were delivered to East Africa by the Bantu Dispersals.

{However, Supporting this suggestion, all of the L2a types in the Hadramawt

Occur at Elevated Frequency in the

Bantu Speakers of Mozambique.}

(Pereira et al. 2001; Salas et al. 2002).

Moreover, the chief L1a type in the Hadramawt also occurs at elevated frequency in

Bantu Speakers and is implicated in

The Bantu Dispersals, albeit having been picked up in East Africa en route.

(Salas et al. 2002). (Bantu languages)

Bantu Speakers are thought to have become first established to the East of the

Great Lakes region somewhat <2,000 years ago (Phillipson 1993).

Assuming that the sub-Saharan African input into Arabia is indeed directly from East Africa

(rather than including a component from west or southeastern Africa), as is most likely on historical and geographical grounds (Segal 2001),

This again limits the main spread into Arabia to within the last ~2,000 years.



Extensive Female-Mediated Gene Flow from Sub-Saharan Africa into Yemen and West Asia …

BioMed Central | Full text | Mitochondrial DNA structure in the Arabian Peninsula …

Eurasian And African mtDna in Saudi Arabian Population.text

Mitchondrial Sequences of Mali and Mauritania.pdf

Hadhramaut – Wikipedia, the free encyclopedia

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