Archive for the Africa Category

Egyptian Y-Chromosomes Indigenous to North Africa and Nile Valley ኒለ ቫልለይ: My Fathers’ Haplogroup E Family: E-PN2= M78, M35, M2/E-V38. The Egyptian Triad Paternal DNA

Posted in afri asiatic, Africa, African Diaspora, Afro Arabs, afro asiatic, Ancient Greece, anthrolpology, Asia and Europe.., Asiatic African, Asiatic African mtdna in Europeans, Beja, Blood type O, Cushitic, Declaration of the Rights of indigenous people, DNA, Dna Bill S.1858 ( Biometrics), Do you have a Nationality ?, Egypt, Egypt and the Blue Nile, Indigenous Y-chromosomes (father's) Dna in Egypt/Nubia, Kushites, Macedonian, National DNA Database in the U.S.A, Nile Valley/Nubia, Nilo Saharan, North Africa, Nubians, O-positive blood, Sahara, Sephardic Hebrews, Sephardic Jews, Sudan, Supra-Sahara, Ta-Seti with tags , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , on April 29, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

King Thutmose. III the 18th Dynasty

king-tut

800px-maler_der_grabkammer_des_ramose_002 Egyptian Y-chromosome Diversity @ Luxor

This is more focused on the Egyptians around Luxor, where Upper Egypt was located.

A recent DNA study by Cruciani that focused on the Y chromosome E-M78 revealed that it was ’born’ in North East Africa , not East Africa as previously thought. This means, that an Egyptianwith an M78Y chromosome has had a male line ancestry reaching back to the Pleistocene inhabitants of Egypt; as far back as the Halfan culture about 24,000 years ago.

Below is a display of the most prevalent among Egyptian Males..

Keita-Boyce Study on Y-chromosomes of Egypt

http://ingiagzennay.free.fr/Keita-Boyce.pdf

http://wysinger.homestead.com/keita6.pdf

Ychromosome (IV) E-M2 is diversified with (1.2%)Lower Egypt, (27.3%)Upper Egypt. And ( 39.1% ) -in Lower Nubia/Nile Valley.

Y-chromosome (XI) E-M35 is diversified with (11.7%)Lower Egypt, (28.8%)Upper Egypt. And (30.4%) in Lower Nubia/Nile Valley.

Y-chromosome (V) E-M78 is diversified with (51.9%)Lower Egypt, (24.2%) – Upper Egypt. And (17.4%) in Lower Nubia/Nile Valley.

(Which group belongs to your father ?)….

The M2 lineage is mainly found primarily in ‘‘Eastern,’’ ‘‘sub-Saharan,’’ and sub-equatorial African groups, those with the highest frequency of the ‘‘Broad’’ trend physiognomy, but found also in notable frequencies in Nubia and Upper Egypt, as indicated by the

RFLP TaqI 49a, f variant IV (see Lucotte and Mercier, 2003; Al-Zahery et al. 2003 for equivalences of markers), which is affiliated with it.

Results show that out of three Egyptian triad M78, M35 and M2, Y-chromosome

M78 has the Highest frequency in Northern lower Egypt @ 51.9%

M35 has the slight Highest frequency  in Southern Upper Egypt @ 28.8%

M2 has the Highest frequency  in Northern and Southern Nubia @ 39.1%.

M2 is virtually absent in North Africa’s lower Egypt at 1.2% and grows to a higher frequency traveling south-bound towards Upper Egypt and Nile valley’s Nubia.

Senusret III 12th Dynasty. triad statue. Middle Kingdom Egypt.. ( the British Museum )

The distribution of these markers in other parts of Africa has usually been explained by the Bantu migrations?

But their presence in the Nile Valley in Non- Bantu speakers cannot be explained in this way...

Their existence is better explained by their being present in populations of the “Early Holocene Sahara”,

who went on to people the Nile Valley in

The mid-Holocene era (12,000 B.P.) according to Hassan (1988);

This occurred way long before the ‘‘Bantu migrations,’’

which also do not explain the high frequency of M2 in Senegal, since there are No Bantu speakers there either.”

Haplogroup M2 also coincides with Egyptian/Nubian Halfan Culture 24,000 B.C. http://en.wikipedia.org/wiki/Halfan

The Halfan people, of Egypt and Nubia flourished between 18,000 and 15,000 BC in Nubia and Egypt.

One Halfan site is dated, before 24,000 BC.

M2- (20,000-30,000 B.P.)

M35- (22,400 B.P.)

M78 (18,600 B.P.)

This would also give the plausible assignment of the Nubian-M2 and the Ethiopian PN2 (35,000 B.P.) as the

“Progenitors” of  Nubian-Egyptian/Halfan Culture”..

They lived on a diet of large herd animals and the Khormusan tradition of fishing.

Although there are only a few Halfan sites and they are small in size, there is a greater concentration of artifacts, indicating that this was not a people bound to seasonal wandering, but one that had settled, at least for a time.

The Halfan is seen as the parent culture of the Ibero-Maurusian industry which spread across the Sahara and into Spain.

Sometimes seen as a Proto-Afro-Asiatic culture, this group is derived from “The Nile River Valley culture known as Halfan”, dating to about 17,000 BC.

The Halfan culture was derived in turn from the Khormusan, which depended on specialized hunting, fishing, and collecting techniques for survival…

The material remains of this culture are primarily stone tools, flakes, and a multitude of rock paintings.

The end of the Khormusan came around 16000 B.C. and was concurrent with the development of other cultures in the region, including the Gemaian.

[S. Keita, “Exploring Northeast African Metric Craniofacial Variation at the Individual Level: A Comparative Study Using Principal Components Analysis,” AMERICAN JOURNAL OF HUMAN BIOLOGY 16:679–689 (2004)]

Mummified Ramesses III 20th Dynasty

Mummified Ramesses III 20th Dynasty “New Kingdom”

Ancient Y-DNA samples shows Egyptian Pharaoh Ramesses III of the 20th Dynasty belonged to Haplogroup  E1b1a/M2/E-V38:

King Ramesses III of Egypt reigned from about 1187 until 1156 BC , but his death has been shrouded in mystery.

Ramesses III

According to a genetic study in December 2012, Ramesses III, second Pharaoh of the Twentieth Dynasty and considered to be the Last Great New Kingdom king to wield any substantial authority over Egypt, belonged to Y-DNA Haplogroup E1b1a/M2/E-V38, mainly found in North Africa, East Africa and  Sub-saharan Africa.

Ramsses III from tomb KV11,

Ramsses III from tomb KV11,

A genetic kinship analysis was done to investigate a possible family relationship between Ramesses III and Unknown man E, Who may actually be his son Pentawer. An ancient Egyptian Prince of the 20th dynasty, and son of Pharaoh Ramesses III and a secondary wife, Tiye. They amplified 16 Y-chromosomal, short tandem repeats (AmpF\STR yfiler PCR amplification kit; Applied Biosystems). Eight polymorphic microsatellites of the nuclear genome were also amplified (Identifiler and AmpF\STR Minifiler kits; Applied Biosystems). The Y-chromosomal Haplogroups of Ramesses III and unknown man E was screened using the Whit Athey’s Haplogroup Predictor we determined the Y-chromosomal Haplogroup E1b1a. The testing of polymorphic autosomal micro satellite loci provided similar results in at least one allele of each marker (table 2⇓). Although the mummy of Ramesses III’s wife Tiy was not available for testing, the identical Ychromosomal DNA and Autosomal half allele sharing of the two male mummies strongly suggest a Father-Son relationship.

Ramesses III-KhonsuTemple-Karnak

Ramesses III-KhonsuTemple-Karnak

http://www.academia.edu/2308336/Revisiting_the_harem_conspiracy_and_death_of_Ramesses_III_anthropological_forensic_radiological_and_genetic_study

Thutmose III the 18th Dyanasty (marble display)

Egyptian total presence of indigenous y-chromosomes haplogroup E familia

(egypt/nubia nile valley)…

(M78-94%,/ M35-71%,/ M268%).

NOTE:

M2 collective Nubian-Egyptian 67.6% with the Addition of Eastern Tutsi’s @ 80%, as well as 52% among the

Kenyan Males and 3.4% with E-thi-op-iansGarners Haplogroup M2 a Clear Unequivocal 203. % Eastern Distribution...

Tutsi M2 is 80% and Kenyans 52% Haplogroup E/M2 bidirectional migration

http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1182266 (copy and paste, if link above is inactive)..

(click link below for chart to see PN2 =

articlerender.fcgi

(M2/M191) at 48% and (M2/PN1) at 32% for Tutsi (M2) total at 80% Eastern Distribution.

( the Nilotic Valley Family: from the White Nile to the Blue Nile)…...

(click in link below to view Nubian-Egyptian 67.6 % of M2 known as variant IV)

Haplogroup M2 ( IV ) Y-Chromosome Variation. Egyptian study.pdf

Y-chromosome haplotypes analyzed in the Nile River Valley in Egypt in 274 unrelated Males, using the p49a,f TaqI polymorphism.

Revealedthese individuals were born in Three regions along the nile river:

in Alexandria (the Delta and Lower Egypt),

in Upper Egypt, and in (Nile Valley’s)Lower Nubia.

Fifteen different p49a,f TaqIhaplotypes are present in Egypt,

The Three most “common” being

Haplotype V (39.4%),

Haplotype XI (18.9%),

Haplotype IV (13.9%).

Haplotype V is  of theHorn/Supra Saharapopulations, with a northern geographic distribution in Egypt in the Nile River Valley.

Haplotype XIhas a characteristic of theHorn/ Supra and Sub-Sahara populations, with a geographic distribution inthe Hornand Nile Valley.

Haplotype IV, has a characteristic of EasternSub-Saharan populations, shows a southern geographic distribution in UpperEgypt and Nubia.

Am J Phys Anthropol 121:000-000, 2003. © 2003 Wiley-Liss, Inc.

Nubian Village along NileHaplogroup E’s    (E3a/E3b) at positions: Dys388-12*, Dys393-14, Dys392-11 and Dys391-10*, Dys426-11*, Dys439-10*

also has high frequencies of:

Jerbian Hebrews from (North-Africa) Carthage/Tunisia’s IslandJerba.” As well as:

Sephardic-Hebrews”  Judaeo-Christians at  8.4 – 12. % North-Africa .

example: (Mauretania-8.0%,  Morocco-8.8%,  Algeria-8.5%,  Libya-7.9%  and  Iberia 5-10% ..)

The Western Distribution of M2 show 80% in Senegal Males and as well as a Southern Distribution in the Khoisan at 17.9% with

A small percentage of  3.4% In Ethiopians while the Brother clade M191 is 1% in Senegalese and 0% in Ethiopians..

{Click link below to view Chart of PN1-M2/E3a Family Quad}

(M191), (M154)(M180/M2) and (M58). articlerender.fcgi

Ethiopians and Khoisan Share the Deepest Clades of the Human Y -Chromo Phylogengy:

(copy and paste in browser)

http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=384897

Modern day genetic studies on they-chromosome also show the Tutsi Males to be 100% of African origin @ http://en.wikipedia.org/wiki/Tutsi

(80% M2/E1b1a, 15% B, 4% E3, 1% M35/E1b1b)…

Tutsi 48% (M2-M191) and 32% (M2-E3a) = 80% M2 lineage..

(click link to see Chart) articlerender.fcgi

When taken in context with previous studies, the current NRY data seem to reflect the linguistic boundaries demarcating

Southern Kenya as the Northern limit of the “Bantu speakers” as they progressed eastward through

The Central African corridor and southward along the Swahili coast.

The Eastern Population in Kenya displays an E3a-M2 frequency of 52%,  (Underhill et al. 2000😉

About 20% of the Y chrom0somes are Near Eastern in Origin, and 10.5 % are Haplogroup R Y– chromosomes.

Some of these African-Asiatic, Asian and Euro Y chromosomes show an ancient entry to Africa

(G, K2, R1a, R1b and R1b1a are8,000 B.P. and older)

The AfriAsiatic Haplogroup R* and family also have percentages from 3%-6.8%

( R*, R1a1 and R1b ) in lower and Upper Egypt combined 12.9%, and is virtually absent in Nile valley’s Nubia 0.0%.

Which is in contrast of the Yemen and West Asia frequencies 10% or higher.

Southern Egyptians Y Chromomses are mainly native to Africa, both sub and supra Saharan.

This makes a grand total of 80.3% definitively African non-Arab ancestry in the upper Egypt region.

Y-chromosomes possibly attributable to Arabmales are very much in the minority in this area.

A rough estimate (since no women invaded Egypt) is that about 5% or less of this population are from

Non Dynastic Egyptian peoples, and

not all of these would be Arabs.

Senusret III

http://www.thegeneticatlas.com

E1b1a (V100) This population is one of two important populations to spring out of the Ethiopian Plateau, E1b1a effect became the most dominant population in Subsaharan Africa

E1b1a (M2) This population grew in enough numbers in the Ethiopian lowlands to be able to cross into the territories of Paleo Africans on their West in Sudan E1b1a (L576) This population represents an East to West thrust in Africa, only E1b1a lineage able to survive crossing the A1b1 territories E1b1a (L86.1) This mutation indicates that the population crossed the A1b1 dominated Grassland into the regions West of the great Lakes E1b1a (M58) Expansion between the Great Lakes & Midwest Africa E1b1a (M116.2) Very small minority in Mali E1b1a (M149) Very small minority in South Africa E1b1a (M155) Very small minority in Mali E1b1a (M10) Dispersed between Cameroon & Tanzania E1b1a (L485) An important lineage that emerged in the Eastern Benue valley in Central Nigeria E1b1a (L514) Marker for a strong lineage that played a major role in turning West Africa into their new territor E1b1a (M191) This marker indicates that the main body of (L485) reached the Benue River in Nigeria and Cameroon E1b1a (P252) A population that followed the Benue river South, an important marker of the Bantu expansion in Nigeria E1b1a (P9.2) The population that remained in the Benue region, expanded into West into Nigeria & South to Gabon E1b1a (P115) Eastern limit expansion population, reaching Southwestern Central Africa, with possible presence in other Fang regions E1b1a (P116) South of the Benue expansion in Southern Cameroon & Gabon E1b1a (U175) An important lineage that emerged in the Western region of Benue in Nigeria and Niger E1b1a (U209) This population represents the backbone of the Bantu expansion, emerged and expanded out of the Bantu Urheimat E1b1a (U290) A primary marker of African slavery in the USA, Important lineage in Southern Cameroon E1b1a (M154) Found in Western Cameroon & South Africa E1b1a (P268) Found in Gambia, could possibly indicate an early expansion out of Central Africa or late emergence out of an L86.1* that lived amongst (L485) or (U175) E1b1a (M329) The E1b1a population that remained in the Ethiopian lowlands.

_______________________

Kushite Prince Horkhemet of Nubia

Kushite Prince Horkhemet of Nubia

_

Kushite Prince Horkhemet of Nubian Dynasty Son of Shabako

Kushite Prince Horkhemet of Nubian Dynasty Son of Shabako

______________________________________________ Continue reading

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Belay Zeleke በላይ ዘለከ The Patriot and Last Hero of Abyssinia-Ethiopia…

Posted in Africa, Ethiopia, Habeshas, The Axumite Kingdom with tags , , , , , , , , , , , , , , , , , , , , on April 27, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

Belay Zeleke በላይ ዘለከ was born in 1896 in the Wollo province of Ethiopia to a mother of Wollo Borena and to a father of Gojam Berenta Origins.  At a very young age in a mysterious situation, Belay Zeleke killed his uncle which prompted him to flee his village and live as a fugitive isolated from his family and friends for the subsequent 15 years.  In his solitary life, Belay Zeleke learned to be courageous and decisive.

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Abyssinian- Italian War in Adwa 1896

Italio- Abyssinian War of Adowa 1896

Subsequently in 1896, Benito Mussolini, the Prime Minister from Italy had suffered a humiliating defeat in Ethiopia (Abyssinia) at the hands of the Negus King Menelik II .

Negus-King of Ethiopia Emperor_Menelik_II

Italian forces were demolished by Ethiopian army forces at the Battle of Adwa. Over ten thousand Italians lay dead. The defeat was victorious for Ethiopians, and yet disastrous for Italian expansion in Africa.

Italy’s humiliation and trample had not been overlooked. The memory of Adwa’s victory sustained, and they felt the need to strike.

Mussolini the modern Caesar of his day, puts his attention toward Ethiopia. He saw this conquest as a means of restoring Roman grandeur.

On October 3, 1935, the Italian dictator launches his first foreign military adventure. He invades the kingdom of Ethiopia as the League of Nations (currently called The United Nations) weakly stands by.

Italy- Abyssinian War of Adowa 1896

Italy- Abyssinian War of Adowa 1896

In 1935 Italy invaded Ethiopia.  Like the many patriotic Ethiopians, Belay Zeleke felt the need to defend his country and led an insurgency movement against the occupation in Gojam.  Soon, he became known for being remorseless among Italian generals and they fought him as hard as they could. Not only did he defeat the Italian army that was sent to destroy him, he also took into custody the army’s general and executed him by hanging.  After driving the Italian army out of Gojam and some parts of Wollo, he put himself in charge of these particular regions much to the gladness of the population.  His courageous heroism inspired thousands of Ethiopians to resist the occupation and many wanted to be like him.

The Ethiopian patriots librated Addis Ababa on 6 May 1941 and this victory officially ended Italian occupation. Fascist Italy’s attempts to colonize Ethiopia came to an abrupt end on this day. Emperor Haile Selassie returned to Addis Ababa on 5 May 1941 after spending the preceding 5 years in exile in Europe. This particular victory was realized as a result of the world-famous swift resistance by Ethiopian patriots.  The contributions made by Belay Zeleke to the struggle and ultimately to the victory of Ethiopia against the colonialist aggression of Fascist Italy were enormous.

Throughout Ethiopia, – particularly in Addis Ababa – signs of Italian presence in the past remain intact to date.  Yet unlike most of the different parts of Ethiopia, there are no physical signs of Italian invasion in the province of Gojjam.  It is believed that Belay Zeleke never let the Italian troops camp anywhere in Gojam let alone build construction to leave a legacy of any sort.

 

Belay Zeleke from Gojam Ethiopia

Belay was so successful in stopping the Italians, that his fellow country men gave him the grand title of  Le’ul Belay or Princely Belay. They also gave him the name and title Atse Bagulbatu which means “Self Made Emperor”. Belay replied, that he did not need any further name or title, as his mother already named him Belay.

His name Belay simply means “One who is Above Others

Upon the Emperor Haile Selassie’s victorious return to Ethiopia in 1941, Belay Zeleke was put in charge of a small region in Gojam when he had assumed a higher rank to be able to play a much bigger role in reconstructing and administering the region.

He declined the position in protest and started living life as an outlaw.  Soon he was caught and sent to jail accused of being a threat to the monarchy.  After making unsuccessful attempts to break out of jail, the patriot Belay Zeleke and his brother Ejjegu was then brutally executed by public hanging on January 12, 1945. His execution was bitterly received by many Ethiopians. In his honor Gojjam road was named after him.

In a heartbreaking error of judgment, an Ethiopian hero who gave the country freedom was given death in return.  And it will always be remembered as an act of giving a National Hero a grave injustice.

Belay Zeleke Ethiopian Patriot

REFERENCES:

http://www.ambaras.com/2014/12/02/belay-zeleke/

Capital Ethiopia News – Sculpture of Hero Erected

Belay Zeleke, The last Hero of Ethiopia | Abesha United.com – the …

ETHIOPIAN OF THE MILLENNIUM – NOMINEES – ETHIOPIAN PATRIOTS, BELAY …

Modern Human Variation: Distribution of Blood Types Americas, Africa, Asia and Europe..

Posted in A-positive blood, AB-Postive blood, Africa, Asia and Europe.., B-postive blood, Blood type O, Blood Types Americas, O-positive blood with tags , , , , , on April 23, 2009 by Biléh* Gambéla በላይ ። ጋምበላ🇺🇸🇸🇩🇨🇻

Distribution of Blood Types


Blood provides an ideal opportunity for the study of human variation without cultural prejudice.  It can be easily classified for many different genetically inherited blood typing systems.  Also significant is the fact that we rarely take blood types into consideration in selecting mates.  In addition, few people know their own type today and no one did a century ago.  As a result, differences in blood type frequencies around the world are most likely due to other factors than social discrimination.  Contemporary Japan is somewhat of an exception since there are popular Japanese stereotypes about people with different blood types.  This could affect choice in marriage partners for some Japanese.

All human populations share the same 27 known blood systems, although they differ in the frequencies of specific types.  Given the evolutionary closeness of apes and monkeys to our species, it is not surprising that some of them share a number of blood typing systems with us as well.

When we donate blood or have surgery, a small sample is usually taken in advance for at least ABOclick this icon to hear the preceding term pronounced and Rh click this icon to hear the preceding term pronounced systems typing.  If you are O+, the O is your ABO type and the + is your Rh type.  It is possible to be A, B, AB, or O as well as Rh+click this icon to hear the preceding term pronounced or Rhclick this icon to hear the preceding term pronounced.  You inherited your blood types from your parents and the environment in which you live can not change them.

We have learned a good deal about how common each of the ABO and RH blood types is around the world.  It is quite clear that the distribution patterns are complex.  Both clinal anddiscontinuous distributions exist, suggesting a complicated evolutionary history for humanity.  This can be seen with the global frequency patterns of the type B blood allele (shown in the map below).  Note that it is highest in Central Asia and lowest in the Americas and Australia.  However, there are relatively high frequency pockets in Africa as well.  Overall in the world,B is the rarest ABO blood allele.  Only 16% of humanity have it.

map of the world showing the frequency of the B blood allele among indigenous populations--it was absent in Australia, New Zealand, and most of the New World except for western Alaska; it was present throughout the Old World with its highest frequencies in Central and East Asia
Distribution of the B type blood allele in native populations of the world

The A blood allele is somewhat more common around the world than B.  About 21% of all people share the A allele. The highest frequencies of A are found in small, unrelated populations, especially the Blackfoot Indians of Montana (30-35%), the Australian Aborigines (many groups are 40-53%), and the Lapps, or Saami people, of Northern Scandinavia (50-90%).  The A allele apparently was absent among Central and South American Indians.

map of the world showing the frequency of the A blood allele among indigenous populations--it was absent in Central and South America, but present throughout the rest of the world; it was at its highest frequency in Western Europe, Australia, and the sub-arctic regions of North America and Greenland
Distribution of the A type blood allele in native populations of the world

The O blood type (usually resulting from the absence of both A and B alleles) is very common around the world.  About 63% of humans share it.  Type O is particularly high in frequency among the indigenous populations of Central and South America, where it approaches 100%.  It also is relatively high among Australian Aborigines and in Western Europe (especially in populations with Celtic ancestors).  The lowest frequency of O is found in Eastern Europe and Central Asia, where B is common.

map of the world showing the frequency of the O blood allele among indigenous populations--most regions were 50% or higher in frequency; it was highest in the New World (90-100%) and lowest in Central Asia (50-60%)
Distribution of the O type blood in native populations of the world

The distribution patterns for the Diego click this icon to hear the preceding term pronounced blood system are even more striking.  Evidently, all Africans, Europeans, East Indians, Australian Aborigines, and Polynesians are Diego negative.  The only populations with Diego positive people may be Native Americans (2-46%) and East Asians (3-12%).  This nonrandom distribution pattern fits well with the hypothesis of an East Asian origin for Native Americans.


Conclusion

These patterns of ABO and Diego blood type distributions are not similar to those for skin color or other so-called “racial” traits.  The implication is that the specific causes responsible for the distribution of human blood types have been different than those for other traits that have been commonly employed to categorize people into “races.”  Since it would be possible to divide up humanity into radically different groupings using blood typing instead of other genetically inherited traits such as skin color, we have more conclusive evidence that the commonly used typological model for understanding human variation is scientifically unsound.

The more we study the precise details of human variation, the more we understand how complex are the patterns.  They cannot be easily summarized or understood.  Yet, this hard-earned scientific knowledge is generally ignored in most countries because of more demanding social and political concerns.  As a result, discrimination based on presumed “racial” groups still continues.  It is important to keep in mind that this “racial” classification often has more to do with cultural and historical distinctions than it does with biology.  In a very real sense, “race” is a distinction that is created by culture not biology.


This page was last updated on Sunday, February 01, 2009.
Copyright © 1998-2009 by Dennis O’Neil. All rights reserved.

illustration credits

Link pasted below:

Modern Human Variation: Distribution of Blood Types


ቢልልይ ጋምበላ