In Jewish tradition, Jewish ancestry is traced to the Biblical patriarchs Abraham, Isaac and Jacob in the second millennium BCE. The modern State of Israel defines itself as a Jewish state in its Basic Laws, and is the only country where Jews are a majority of the population. Jews also experienced political autonomy twice during ancient history. The first of the two ancient eras spanned from 1350 to 586 BCE, and encompassed the periods of the Judges, the United Monarchy, and the Divided Monarchy of the Kingdoms of Israel and Judah, ending with the destruction of the First Temple. The second era was the period of the Hasmonean Kingdom spanning from 140 to 37 BCE. Since the destruction of the First Temple, the diaspora has been the home of most of the world's Jews. Except in Israel, Jews are a minority in every country in which they live, and they have frequently experienced persecution throughout history, resulting in a population that fluctuated both in numbers and distribution over the centuries.
, the world Jewish population was estimated at 13.42 million by the North American Jewish Data Bank, or roughly 0.2% of the total world population. According to this report, about 42% of all Jews reside in Israel (5.70 million), and about 42% in the United States (5.28 million) and Canada (0.38 million), with most of the remainder living in Europe (1.46 million). These numbers include all those who consider themselves Jews, whether or not they are affiliated with a Jewish organization. The total world Jewish population, however, is difficult to measure. In addition to issues with census methodology, there are ''halakhic'' disputes regarding who is a Jew and secular, political, and ancestral identification factors that may affect the figure considerably.
The English word ''Jew'' continues Middle English '''', a loan from Old French '''', earlier '''', ultimately from Latin ''''. The Latin '''' simply means ''Judaean'', "from the land of ''Judaea''". The Latin term itself, like the corresponding Greek , is a loan from Aramaic '''', corresponding to , ''Yehudi'' (sg.); , ''Yehudim'' (pl.), in origin the term for a member of the tribe of Judah or the people of the kingdom of Judah. The name of both the tribe and kingdom derive from Judah, the fourth son of Jacob.
The Hebrew word for Jew, ISO 259-3 Yhudi, is pronounced , with the stress on the final syllable, in Israeli Hebrew, in its basic form.
The Ladino name is , ''Djudio'' (sg.); , ''Djudios'' (pl.); : ''Yid'' (sg.)}}; , ''Yidn'' (pl.).
The etymological equivalent is in use in other languages, e.g., "Yahoud"/"Yahoudi" () in Arabic language "Jude" in German, "juif" in French, "jøde" in Danish, "judío" in Spanish, etc., but derivations of the word "Hebrew" are also in use to describe a Jew, e.g., in Italian (''Ebreo''), in Persian language ("Ebri/Ebrani" ()) and Russian (''Еврей, Yevrey''). The German word "Jude" is pronounced , and is the origin of the word Yiddish. (See Jewish ethnonyms for a full overview.)
According to ''The American Heritage Dictionary of the English Language'', Fourth Edition (2000):
It is widely recognized that the attributive use of the noun ''Jew'', in phrases such as ''Jew lawyer'' or ''Jew ethics'', is both vulgar and highly offensive. In such contexts ''Jewish'' is the only acceptable possibility. Some people, however, have become so wary of this construction that they have extended the stigma to any use of ''Jew'' as a noun, a practice that carries risks of its own. In a sentence such as ''There are now several Jews on the council'', which is unobjectionable, the substitution of a circumlocution like ''Jewish people'' or ''persons of Jewish background'' may in itself cause offense for seeming to imply that Jew has a negative connotation when used as a noun.
Historical definitions of Jewish identity have traditionally been based on ''halakhic'' definitions of matrilineal descent, and halakhic conversions. Historical definitions of who is a Jew date back to the codification of the oral tradition into the Babylonian Talmud. Interpretations of sections of the Tanakh, such as Deuteronomy 7:1–5, by learned Jewish sages, are used as a warning against intermarriage between Jews and non-Jews because "[the non-Jewish husband] will cause your child to turn away from Me and they will worship the gods of others." Leviticus 24:10 says that the son in a marriage between a Hebrew woman and an Egyptian man is "of the community of Israel." This contrasts with Ezra 10:2–3, where Israelites returning from Babylon vow to put aside their gentile wives and their children. Since the ''Haskalah'', these ''halakhic'' interpretations of Jewish identity have been challenged.
At times, conversion has accounted for a substantial part of Jewish population growth. In the first century of the Christian era, for example, the population more than doubled, from four to 8–10 million within the confines of the Roman Empire, in good part as a result of a wave of conversion.
Jews are often identified as belonging to one of two major groups: the ''Ashkenazim'', or "Germanics" (Ashkenaz meaning "Germany" in Medieval Hebrew, denoting their Central European base), and the ''Sephardim'', or "Hispanics" (Sefarad meaning "Spain/Hispania" or "Iberia" in Hebrew, denoting their Spanish, and Portuguese, base). The ''Mizrahim'', or "Easterners" (Mizrach being "East" in Hebrew), that is, the diverse collection of Middle Eastern and North African Jews, constitute a third major group, although they are sometimes termed ''Sephardi'' for liturgical reasons.
Smaller groups include, but are not restricted to, Indian Jews such as the Bene Israel, Bnei Menashe, Cochin Jews, and Bene Ephraim; the Romaniotes of Greece; the Italian Jews ("Italkim" or "Bené Roma"); the Teimanim from Yemen and Oman; various African Jews, including most numerously the Beta Israel of Ethiopia; and Chinese Jews, most notably the Kaifeng Jews, as well as various other distinct but now almost extinct communities.
The divisions between all these groups are approximate and their boundaries are not always clear. The Mizrahim for example, are a heterogeneous collection of North African, Central Asian, Caucasian, and Middle Eastern Jewish communities that are often as unrelated to each other as they are to any of the earlier mentioned Jewish groups. In modern usage, however, the Mizrahim are sometimes termed ''Sephardi'' due to similar styles of liturgy, despite independent development from Sephardim proper. Thus, among Mizrahim there are Iraqi Jews, Egyptian Jews, Berber Jews, Lebanese Jews, Kurdish Jews, Libyan Jews, Syrian Jews, Bukharian Jews, Mountain Jews, Georgian Jews, and various others. The Teimanim from Yemen and Oman are sometimes included, although their style of liturgy is unique and they differ in respect to the admixture found among them to that found in Mizrahim. In addition, there is a differentiation made between Sephardi migrants who established themselves in the Middle East and North Africa after the expulsion of the Jews from Spain and Portugal in the 1490s and the pre-existing Jewish communities in those regions.
Despite this diversity, Ashkenazi Jews represent the bulk of modern Jewry, with at least 70% of Jews worldwide (and up to 90% prior to World War II and the Holocaust). As a result of their emigration from Europe, Ashkenazim also represent the overwhelming majority of Jews in the New World continents, in countries such as the United States, Canada, Argentina, Australia, and Brazil. In France, emigration of Jews from North Africa has led them to outnumber the Ashkenazim . Only in Israel is the Jewish population representative of all groups, a melting pot independent of each group's proportion within the overall world Jewish population.
Hebrew is the liturgical language of Judaism (termed ''l'shon ha-kodesh'', "the holy tongue"), the language in which the Hebrew scriptures (Tanakh) were composed, and the daily speech of the Jewish people for centuries. By the 5th century BCE, Aramaic, a closely related tongue, joined Hebrew as the spoken language in Judea. By the third century BCE, Jews of the diaspora were speaking Greek.
For centuries, Jews worldwide have spoken the local or dominant languages of the regions they migrated to, often developing distinctive dialectal forms or branches that became independent languages. Yiddish is the Judæo-German language developed by Ashkenazi Jews who migrated to Central Europe. Ladino is the Judæo-Spanish language developed by Sephardic Jews who migrated to the Iberian peninsula. Due to many factors, including the impact of the Holocaust on European Jewry, the Jewish exodus from Arab lands, and widespread emigration from other Jewish communities around the world, ancient and distinct Jewish languages of several communities, including Gruzinic, Judæo-Arabic, Judæo-Berber, Krymchak, Judæo-Malayalam and many others, have largely fallen out of use.
For over sixteen centuries Hebrew was used almost exclusively as a liturgical language, and as the language in which most books had been written on Judaism, with a few speaking only Hebrew on the Sabbath. Hebrew was revived as a spoken language by Eliezer ben Yehuda, who arrived in Palestine in 1881. It had not been used as a mother tongue since Tannaic times. Modern Hebrew is now one of the two official languages of the State of Israel along with Arabic.
The three most commonly spoken languages among Jews today are Hebrew, English and Russian. Some Romance languages, such as French and Spanish, are also widely used.
Yiddish has been spoken by more Jews in history than any other language, but it is far less used today, after the Holocaust and the adoption of Hebrew by the Zionist movement, then Israel.
Genetic studies indicate various lineages found in modern Jewish populations; however, most of these populations share a lineage in common, traceable to an ancient population that underwent geographic branching and subsequent independent evolutions. While DNA tests have demonstrated inter-marriage in all of the various Jewish ethnic divisions over the last 3,000 years, it was substantially less than in other populations. The findings lend support to traditional Jewish accounts accrediting their founding to exiled Israelite populations, and counters theories that many or most of the world's Jewish populations were founded entirely by local populations that adopted the Jewish religion, devoid of any actual Israelite genetic input.
DNA analysis further determined that modern Jews of the priesthood tribe—"Kohanim"—share an ancestor dating back about 3,000 years. This result is consistent for all Jewish populations around the world. The researchers estimated that the most recent common ancestor of modern Kohanim lived between 1000 BCE (roughly the time of the Biblical Exodus) and 586 BCE, when the Babylonians destroyed the First Temple. They found similar results analyzing DNA from Ashkenazi and Sephardi Jews. The scientists estimated the date of the original priest based on genetic mutations, which indicated that the priest lived roughly 106 generations ago, between 2,650 and 3,180 years ago depending whether one counts a generation as 25 or 30 years. These Jews belong to the haplotypes J1e and J2a. However, more recent research has shown that many ethnic groups in the Middle East and Mediterranean area also share this genetic profile.
Although individual and groups of converts to Judaism have historically been absorbed into contemporary Jewish populations, it is unlikely that they formed a large percentage of the ancestors of modern Jewish groups, and much less that they represented their genesis as Jewish communities.
Biologist Robert Pollack stated in 2003 that one cannot determine the biological "Jewishness" of an individual because "there are no DNA sequences common to all Jews and absent from all non-Jews". A 2009 study was able to genetically identify individuals with full or partial Ashkenazi Jewish ancestry.
Other Y-chromosome findings show that the world's Jewish communities are closely related to Kurds, Syrians and Palestinians. Skorecki and colleague wrote that "the extremely close affinity of Jewish and non-Jewish Middle Eastern populations observed ... supports the hypothesis of a common Middle Eastern origin". According to another study of the same year, more than 70% of Jewish men and half of the Arab men (inhabitants of Israel and the territories only) whose DNA was studied inherited their Y-chromosomes from the same paternal ancestors who lived in the region within the last few thousand years. The results are consistent with the Biblical account of Jews and Arabs having a common ancestor. About two-thirds of Israeli Arabs and Arabs in the territories and a similar proportion of Israeli Jews are the descendants of at least three common ancestors who lived in the Middle East in the Neolithic period. However, the Palestinian Arab clade includes two Arab modal haplotypes which are found at only very low frequency among Jews, reflecting divergence and/or large scale admixture from non-local populations to the Palestinians.
A study of haplotypes of the Y-chromosome, published in 2000, addressed the paternal origins of Ashkenazi Jews. Hammer ''et al.'' found that the Y chromosome of some Ashkenazi and Sephardi Jews contained mutations that are also common among Middle Eastern peoples, but uncommon in the general European population. This suggested that the male ancestors of the Ashkenazi Jews could be traced mostly to the Middle East. The proportion of male genetic admixture in Ashkenazi Jews amounts to less than 0.5% per generation over an estimated 80 generations, with "relatively minor contribution of European Y chromosomes to the Ashkenazim," and a total admixture estimate "very similar to Motulsky's average estimate of 12.5%." This supported the finding that "Diaspora Jews from Europe, Northwest Africa, and the Near East resemble each other more closely than they resemble their non-Jewish neighbors." However, when all haplotypes were included in the analysis, m (the admixture percentage) increased to 23% ± 7%. In addition, of the Jewish populations in this cluster, the Ashkenazim were closest to South European populations, specifically the Greeks.
In Jewish populations, Haplogroup J1 (defined by the 267 marker) constitutes 30% of the Yemenite Jews 20.0% of the Ashkenazim results and 12% of the Sephardic results. However, J1 is most frequent in Yemen (76%), Saudi (64%) Qatar (58%). J1 is generally frequent amongst Negev Bedouins (62%). It is also very common among other Arabs such as those of the Levant, i.e. Palestinian (38.4%), Syria (30%), Lebanon (25%). In Europe, higher frequencies have been reported in the central Adriatic regions of Italy: Gargano (17.2%), Pescara (15%), in the Mediterranean Paola (11.1%) and in South Sicilian Ragusa (10.7%). Fairly high frequencies have also been reported in other nearby Mediterranean areas: Crete (8.3%), Malta (7.8%), Cyprus (6.2%), Greece (5.3%).
Haplogroup J2 which is found in the Sephardic Jews (29%) and Ashkenazi Jews (23%), or 19%. is found mainly in the Fertile Crescent, the Caucasus, Anatolia, the Balkans, Italy, the Mediterranean littoral, the Iranian plateau, Central Asia, and South Asia. More specifically, it is found in Iraq, Syria, Lebanon, Turkey, Israel, Palestine, Greece, Italy and the eastern coasts of the Iberian Peninsula, and more frequently in Iraqis 29.7%, Lebanese 25%, Palestinians 16.8%, Syrians 22.5%, Kurds 28.4%, Saudi Arabia 15.92%, Jordan 14.3%, Oman 10–15%, UAE 10.4%, Yemen 9.7%, in Israel, in Palestine, and in Turkey.
Research in 2008 found significant founder effects in many non-Asheknazi Jewish populations. In Belmonte, Azerbaijani, Georgian, Bene Israel and Libyan Jewish communities "a single mother was sufficient to explain at least 40% of their present-day mtDNA variation". In addition, "the Cochin and Tunisian Jewish communities show an attenuated pattern with two founding mothers explaining >30% of the variation." In contrast, Bulgarian, Turkish, Moroccan and Ethiopian Jews were heterogeneous with no evidence "for a narrow founder effect or depletion of mtDNA variation attributable to drift". The authors noted that "the first three of these communities were established following the Spanish expulsion and/or received large influxes of individuals from the Iberian Peninsula and high variation presently observed, probably reflects high overall mtDNA diversity among Jews of Spanish descent. Likewise, the mtDNA pool of Ethiopian Jews reflects the rich maternal lineage variety of East Africa." Jewish communities from Iraq, Iran, and Yemen showed a "third and intermediate pattern... consistent with a founding event, but not a narrow one".
In this and other studies Yemenite Jews differ from other Mizrahim, as well as from Ashkenazim, in the proportion of sub-Saharan African gene types which have entered their gene pools. African-specific Hg L(xM,N) lineages were found only in Yemenite and Ethiopian Jewish populations. Among Yemenites, the average stands at 35% lineages within the past 3,000 years.
A 2006 study by Seldin, ''et al.'' used over five thousand autosomal SNPs to demonstrate European genetic substructure amongst the Ashkenazi. The results showed "a consistent and reproducible distinction between 'northern' and 'southern' European population groups". Most northern, central, and eastern Europeans (Finns, Swedes, English, Irish, Germans, and Ukrainians) showed >90% in the 'northern' population group, while most individual participants with southern European ancestry (Italians, Greeks, Portuguese, Spaniards) showed >85% in the 'southern' group. Both Ashkenazi Jews as well as Sephardic Jews showed >85% membership in the "southern" group. Referring to the Jews clustering with southern Europeans, the authors state the results were "consistent with a later Mediterranean origin of these ethnic groups".
A 2007 study by Bauchet, ''et al.'' found that Ashkenazi Jews were most closely clustered with Arabic North African populations when compared to Global population, and in the European structure analysis, they share similarities only with Greeks and Southern Italians, reflecting their east Mediterranean origins.
A 2010 study on Jewish ancestry by Atzmon-Ostrer ''et al.'' stated "Two major groups were identified by principal component, phylogenetic, and identity by descent (IBD) analysis: Middle Eastern Jews and European/Syrian Jews. The IBD segment sharing and the proximity of European Jews to each other and to southern European populations suggested similar origins for European Jewry and refuted large-scale genetic contributions of Central and Eastern European and Slavic populations to the formation of Ashkenazi Jewry.", as both groups - the Middle Eastern Jews and European/Syrian Jews shared common ancestors in the Middle East about 2500 years ago. The study examines genetic markers spread across the entire genome and shows that the Jewish groups (Ashkenazi and non Ashkenazi) share large swaths of DNA, indicating close relationships and that each of the Jewish groups in the study (Iranian, Iraqi, Syrian, Italian, Turkish, Greek and Ashkenazi) has its own genetic signature but is more closely related to the other Jewish groups than to their non Jewish fellow countrymen. Atzmon's team found that the SNP markers in genetic segments of 3 million DNA letters or longer were 10 times more likely to be identical among Jews than non-Jews. Results of the analysis also tally with biblical accounts of the fate of the Jews. Using their DNA analysis, the authors traced the ancestors of all Jews to Persia and Babylon, areas that now form part of Iran and Iraq. The study also found that with respect to non-Jewish European groups, the population most closely related to Ashkenazi Jews are modern-day Italians. The study speculated that the genetic-similarity between Ashkenazi Jews and Italians may be due to inter-marriage and conversions in the time of the Roman Empire. It was also found that any two Ashkenazi Jewish participants in the study shared about as much DNA as fourth or fifth cousins
A 2010 study by Bray ''et al'', using SNP microarray techniques and linkage analysis, estimated that 35 to 55 percent of the modern Ashkenazi genome is specifically traceable to Europe, and that European "admixture is considerably higher than previous estimates by studies that used the Y chromosome". The study assumed Druze and Palestinian Arabs populations to represent the reference to world Jewry ancestor genome. With this reference point, the linkage disequilibrium in the Ashkenazi Jewish population was interpreted as "matches signs of interbreeding or 'admixture' between Middle Eastern and European populations". In their press release, Bray stated: "We were surprised to find evidence that Ashkenazi Jews have higher heterozygosity than Europeans, contradicting the widely-held presumption that they have been a largely isolated group". Nevertheless, the authors indicated possible Achilles heels for their conclusions. These were, firstly, that their calculations might have "overestimated the level of admixture" in case that the true Jewish ancestor was genetically closer to Southern Europeans than Druze and Palestinian Arabs are and, secondly, predicted that using the non Ashkenazi Jewish Diaspora populations as reference for world Jewry ancestor genome will "underestimate the level of admixture". This would be because they find it reasonable that the non-Ashkenazi Jewish Diaspora has also "undergone the similar admixture".
Israel, the Jewish nation-state, is the only country in which Jews make up a majority of the citizens. Israel was established as an independent democratic and Jewish state on May 14, 1948. Of the 120 members in its parliament, the Knesset, currently, 12 members of the Knesset are Arab citizens of Israel, most representing Arab political parties and one of Israel's Supreme Court judges is a Palestinian Arab.
Between 1948 and 1958, the Jewish population rose from 800,000 to two million. Currently, Jews account for 75.8% of the Israeli population, or 5.4 million people. The early years of the state of Israel were marked by the mass immigration of Holocaust survivors and Jews fleeing Arab lands. Israel also has a large population of Ethiopian Jews, many of whom were airlifted to Israel in the late 1980s and early 1990s. Between 1974 and 1979 nearly 227,258 immigrants arrived in Israel, about half being from the Soviet Union. This period also saw an increase in immigration to Israel from Western Europe, Latin America, and the United States
A trickle of immigrants from other communities has also arrived, including Indian Jews and others, as well as some descendants of Ashkenazi Holocaust survivors who had settled in countries such as the United States, Argentina, Australia and South Africa. Some Jews have emigrated from Israel elsewhere, due to economic problems or disillusionment with political conditions and the continuing Arab-Israeli conflict. Jewish Israeli emigrants are known as yordim.
Currently, the largest Jewish community in the world is located in the United States, with 5.3 million to 6.4 million Jews by various estimates. Elsewhere in the Americas, there are also large Jewish populations in Canada, Argentina, and Brazil, and smaller populations in Mexico, Uruguay, Venezuela, Chile, and several other countries (see History of the Jews in Latin America).
Western Europe's largest Jewish community can be found in France, home to 490,000 Jews, the majority of whom are immigrants or refugees from North African Arab countries such as Algeria, Morocco, and Tunisia (or their descendants). There are 295,000 Jews in the United Kingdom. In Eastern Europe, there are anywhere from 350,000 to one million Jews living in the former Soviet Union, but exact figures are difficult to establish. The fastest-growing Jewish community in the world, outside Israel, is the one in Germany, especially in Berlin, its capital. Tens of thousands of Jews from the former Eastern Bloc have settled in Germany since the fall of the Berlin Wall.
The Arab countries of North Africa and the Middle East were home to around 900,000 Jews in 1945. Fueled by anti-Zionism after the founding of Israel, systematic persecution caused almost all of these Jews to flee to Israel, North America, and Europe in the 1950s (see Jewish exodus from Arab lands). Today, around 8,000 Jews remain in all Arab nations combined.
Iran is home to around 10,800 Jews, down from a population of 100,000 Jews before the 1979 revolution. After the revolution some of the Iranian Jews emigrated to Israel or Europe but most of them emigrated (with their non-Jewish Iranian compatriots) to the United States (especially Los Angeles, where the principal community is called "Tehrangeles").
Outside Europe, the Americas, the Middle East, and the rest of Asia, there are significant Jewish populations in Australia and South Africa.
Rates of interreligious marriage vary widely: In the United States, they are just under 50%, in the United Kingdom, around 53%, in France, around 30%, and in Australia and Mexico, as low as 10%. In the United States, only about a third of children from intermarriages affiliate themselves with Jewish religious practice. The result is that most countries in the Diaspora have steady or slightly declining religiously Jewish populations as Jews continue to assimilate into the countries in which they live.
The Jewish people and Judaism have experienced various persecutions throughout Jewish history. During late Antiquity and the early Middle Ages the Roman Empire (in its later phases known as the Byzantine Empire) repeatedly repressed the Jewish population, first by ejecting them from their homelands during the pagan Roman era and later by officially establishing them as second-class citizens during the Christian Roman era.
According to James Carroll, "Jews accounted for 10% of the total population of the Roman Empire. By that ratio, if other factors had not intervened, there would be 200 million Jews in the world today, instead of something like 13 million."
Later in medieval Western Europe, further persecutions of Jews in the name of Christianity occurred, notably during the Crusades—when Jews all over Germany were massacred—and a series of expulsions from England, Germany, France, and, in the largest expulsion of all, Spain and Portugal after the Reconquista (the Catholic Reconquest of the Iberian Peninsula), where both unbaptized Sephardic Jews and the ruling Muslim Moors were expelled.
In the Papal States, which existed until 1870, Jews were required to live only in specified neighborhoods called ghettos. In the 19th and (before the end of World War II) 20th centuries, the Roman Catholic Church adhered to a distinction between "good antisemitism" and "bad antisemitism". The "bad" kind promoted hatred of Jews because of their descent. This was considered un-Christian because the Christian message was intended for all of humanity regardless of ethnicity; anyone could become a Christian. The "good" kind criticized alleged Jewish conspiracies to control newspapers, banks, and other institutions, to care only about accumulation of wealth, etc.
Islam and Judaism have a complex relationship. Traditionally Jews and Christians living in Muslim lands, known as dhimmis, were allowed to practice their religions and to administer their internal affairs, but subject to certain conditions. They had to pay the jizya (a per capita tax imposed on free adult non-Muslim males) to the Islamic state. Dhimmis had an inferior status under Islamic rule. They had several social and legal disabilities such as prohibitions against bearing arms or giving testimony in courts in cases involving Muslims. Many of the disabilities were highly symbolic. The one described by Bernard Lewis as "most degrading" was the requirement of distinctive clothing, not found in the Qur'an or hadith but invented in early medieval Baghdad; its enforcement was highly erratic. On the other hand, Jews rarely faced martyrdom or exile, or forced compulsion to change their religion, and they were mostly free in their choice of residence and profession.
Notable exceptions include the massacre of Jews and/or forcible conversion of some Jews by the rulers of the Almohad dynasty in Al-Andalus in the 12th century, as well as in Islamic Persia, and the forced confinement of Morrocan Jews to walled quarters known as mellahs beginning from the 15th century and especially in the early 19th century. In modern times, it has become commonplace for standard antisemitic themes to be conflated with anti-Zionist publications and pronouncements of Islamic movements such as Hezbollah and Hamas, in the pronouncements of various agencies of the Islamic Republic of Iran, and even in the newspapers and other publications of Turkish Refah Partisi."
Throughout history, many rulers, empires and nations have oppressed their Jewish populations or sought to eliminate them entirely. Methods employed ranged from expulsion to outright genocide; within nations, often the threat of these extreme methods was sufficient to silence dissent. The history of antisemitism includes the First Crusade which resulted in the massacre of Jews; the Spanish Inquisition (led by Torquemada) and the Portuguese Inquisition, with their persecution and ''autos-da-fé'' against the New Christians and Marrano Jews; the Bohdan Chmielnicki Cossack massacres in Ukraine; the Pogroms backed by the Russian Tsars; as well as expulsions from Spain, Portugal, England, France, Germany, and other countries in which the Jews had settled.
The persecution reached a peak in Adolf Hitler's Final Solution, which led to the Holocaust and the slaughter of approximately 6 million Jews from 1939 to 1945. According to a recent study published in the American Journal of Human Genetics 19.8% of the modern Iberian population has Sephardic Jewish ancestry, indicating that the number of conversos may have been much higher than originally thought.
The most notable modern day persecution of Jews remains the Holocaust — the state-led systematic persecution and genocide of European Jews (and certain communities of North African Jews in European controlled North Africa) and other minority groups of Europe during World War II by Nazi Germany and its collaborators. The persecution and genocide were accomplished in stages. Legislation to remove the Jews from civil society was enacted years before the outbreak of World War II.
Concentration camps were established in which inmates were used as slave labour until they died of exhaustion or disease. Where the Third Reich conquered new territory in eastern Europe, specialized units called Einsatzgruppen murdered Jews and political opponents in mass shootings. Jews and Roma were crammed into ghettos before being transported hundreds of miles by freight train to extermination camps where, if they survived the journey, the majority of them were killed in gas chambers. Virtually every arm of Germany's bureaucracy was involved in the logistics of the mass murder, turning the country into what one Holocaust scholar has called "a genocidal nation."
Orthodox and Conservative Judaism discourage proselytism to non-Jews, but many Jewish groups have tried to reach out to the assimilated Jewish communities of the Diaspora in order for them to reconnect to their Jewish roots. Additionally, while in principle Reform Judaism favors seeking new members for the faith, this position has not translated into active proselytism, instead taking the form of an effort to reach out to non-Jewish spouses of intermarried couples.
There is also a trend of Orthodox movements pursuing secular Jews in order to give them a stronger Jewish identity so there is less chance of intermarriage. As a result of the efforts by these and other Jewish groups over the past twenty-five years, there has been a trend of secular Jews becoming more religiously observant, known as the ''Baal Teshuva'' movement, though the demographic implications of the trend are unknown. Additionally, there is also a growing movement of Jews by Choice by gentiles who make the decision to head in the direction of becoming Jews.
There is no single governing body for the Jewish community, nor a single authority with responsibility for religious doctrine. Instead, a variety of secular and religious institutions at the local, national, and international levels lead various parts of the Jewish community on a variety of issues.
Jews have made contributions in a broad range of human endeavors, including the sciences, arts, politics, and business. The number of Jewish Nobel prize winners is far out of proportion to the percentage of Jews in the world's population.
Category:Ancient peoples Category:Ethnic groups in the Middle East Category:Ethno-cultural designations Category:Religious identity Category:Semitic peoples Category:Indigenous peoples of Southwest Asia
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One of the first scholars to perform genetic studies was Luigi Luca Cavalli-Sforza. He used ''classical genetic markers'' to analyse DNA by proxy. This method studies differences in the frequencies of particular allelic traits, namely polymorphisms from proteins found within human blood (such as the ABO blood groups, Rhesus blood antigens, HLA loci, immunoglobulins, G-6-P-D isoenzymes, amongst others). Subsequently his team calculated genetic distance between populations, based on the principle that two populations that share similar frequencies of a trait are more closely related than populations that have more divergent frequencies of the trait. From this, he constructed phylogenetic trees which showed genetic distances diagrammatically. His team also performed principal component analyses, which is good at analysing multivariate data with minimal loss of information. The information that is lost can be partly restored by generating a second principal component, and so on. In turn, the information from each individual principal component (PC) can be presented graphically in ''synthetic maps''. These maps show peaks and troughs, which represent populations whose gene frequencies take extreme values compared to others in the studied area.
Peaks and troughs usually, but not necessarily, connected by smooth gradients, called clines. Genetic clines can be generated in several ways: including adaptation to environment (natural selection), continuous gene flow between two initially different populations, or a demographic expansion into a scarcely populated environment with little initial admixture with pre-existing populations. Cavalli-Sforza connected these gradients with postulated pre-historic population movements based on known archaeological and linguistic theories. However, given that the time depths of such patterns are not known, “associating them with particular demographic events is usually speculative”.
Studies using ''direct DNA analysis'' are now abundant, and may utilize mitochondrial DNA (mtDNA), the non-recombining portion of the Y chromosome (NRY) or autosomal DNA. MtDNA and NRY DNA share some similar features which have made them particularly useful in genetic anthropology. These properties include the direct, unaltered inheritance of mtDNA and NRY DNA from mother to offspring, and father to son, respectively, without the 'scrambling' effects of genetic recombination. We also presume that these genetic loci are not affected by natural selection, and that the major process responsible for changes in base pairs has been mutation (which can be calculated).
The smaller effective population size of the NRY and mtDNA enhances the consequences of drift and founder effect relative to the autosomes, making NRY and mtDNA variation a potentially sensitive index of population composition. However, these biologically plausible assumptions are nevertheless not concrete. For example, Rosser suggests that climatic conditions may affect the fertility of certain lineages. (''See also'' Genetic drift, Founder effect, Population bottleneck.) Greater certainty about chronology may be obtained from studies of ancient DNA (see below), but so far these have been comparatively few.
Whereas Y-DNA and mtDNA haplogroups represent but a small component of a person’s DNA pool, autosomal DNA has the advantage of containing hundreds and thousands of examinable genetic loci, thus giving a more complete picture of genetic composition. However, descent relationships can only to be determined on a statistical basis because autosomal DNA undergoes recombination. A single chromosome can record multiple histories; a separate history for each gene. Autosomal studies are much more reliable for showing the relationships between existing populations but do not offer the possibilities for unraveling their histories in the same way as mtDNA and NRY DNA studies promise, despite their many complications.
Genetic studies operate on numerous assumptions and suffer from usual methodological limitations such as selection bias and confounding. Furthermore, no matter how accurate the methodology, conclusions derived from such studies are ultimately compiled on the basis of how the author envisages their data fits with established archaeological or linguistic theories.
+ Percentage genetic distances among major continents based on 120 classical polymorphisms | Africa | Oceania| | East Asia | Europe | |
Oceania | 24.7| | ||||
East Asia | 20.6| | 10 | |||
Europe | 16.6| | 13.5 | 9.7 | ||
America | 22.6| | 14.6 | 8.9 | 9.5 |
According to Cavalli-Sforza's work, all non-African populations are more closely related to each other than to Africans; supporting the hypothesis that all non-Africans descend from a single old-African population. The genetic distance from Africa to Europe (16.6) was found to be shorter than the genetic distance from Africa to East Asia (20.6), and much shorter than that from Africa to Australia (24.7). He explains:
This particular model used an Out of Africa migration 100,000 years ago which separated Africans from non-Africans followed by a single admixture event 30,000 years ago leading to the formulation of the European population. The admixture event consisted of a source population that was 35% African and 65% East Asian. However the study notes that a more realistic scenario would include several admixture events occurring over a sustained period. In particular they cite the spread of farming from a source population in West Asia 5000–9000 years ago may have played a role in the genetic relatedness of Africans and Europeans since West Asia is sandwiched in between Africa and Central Asia. The model assumed an out of Africa migration 100kya and a single admixture event 30kya. However, most contemporary studies have more recent dates that place the out of Africa migration 50-70kya. The study also involved a direct comparison between Sub-Saharan Africans (Central Africans and Senegalese) and Europeans. North Africans population were omitted from the study as they are known to have both Eurasian and Sub-Saharan admixture. These considerations might help explain the apparent short genetic distance between Europeans and Africans
A later study by Bauchet, which utilised ~ 10 thousand autosomal DNA SNPs arrived at similar results. Principal component analysis clearly identified four widely dispersed groupings corresponding to Africa, Europe, Central Asia and South Asia. PC1 separated Africans from the other populations, PC2 divided Asians from Europeans and Africans, whilst PC3 split Central Asians apart from South Asians.
Geneticists agree that Europe is the most genetically homogeneous of all the continents. However, some patterns are discernible. Cavalli-Sforza’s principal component analyses revealed five major clinal patterns throughout Europe, and similar patterns have continued to be found in more recent studies. #A cline of genes with highest frequencies in the Middle East, spreading to lowest levels northwest. Cavalli-Sforza originally described this as faithfully reflecting the spread of agriculture in Neolithic times. This has been the general tendency in interpretation of all genes with this pattern. #A cline of genes with highest frequencies amongst Finnish and Saami in the extreme north east, and spreading to lowest frequencies in the south west. #A cline of genes with highest frequencies in the area of the lower Don and Volga rivers in southern Russia, and spreading to lowest frequencies in Iberia, Southern Italy, Greece and the areas inhabited by Saami speakers in the extreme north of Scandinavia. Cavalli-Sforza associated this with the spread of Indo-European languages, which he links in turn to a "secondary expansion" after the spread of agriculture, associated with animal grazing. #A cline of genes with highest frequencies in the Balkans and Southern Italy, spreading to lowest levels in Britain and the Basque country. Cavalli-Sforza associates this with "the Greek expansion, which reached its peak in historical times around 1000 and 500 BC but which certainly began earlier" #A cline of genes with highest frequencies in the Basque country, and lower levels beyond the area of Iberia and Southern France. In perhaps the most well-known conclusion from Cavalli-Sforza this weakest of the 5 patterns was described as isolated remnants of the pre-Neolithic population of Europe, "who at least partially withstood the expansion of the cultivators". It corresponds roughly to the geographical spread of rhesus negative blood types. In particular, the conclusion that the Basques are a genetic isolate has become widely discussed, but also a controversial conclusion.
He also created a phylogenetic tree to analyse the internal relationships amongst Europeans. He found four major 'outliers'- Basques, Lapps, Finns and Icelanders; a result he attributed to their relative isolation (note: with the exception of the Icelanders, the rest of the groups speak non-Indo-European languages). Greeks and Yugoslavs represented a second group of less extreme outliers. The remaining populations clustered into several groups : "Celtic", "Germanic", "south-western Europeans", "Scandinavians" and "eastern Europeans".
There are three big Y-chromosome DNA haplogroups which account for most of Europe's patrilineal descent.
Haplogroup R1b is common all over Europe but especially common in Western Europe. Nearly all of this R1b in Europe is in the form of the R1b1b2 (R-M269) sub-clade, specifically within the R-L23 sub-sub-clade whereas R1b found in Central Asia, western Asia and Africa tends to be in other clades. It has also been pointed out that outlier types are present in Europe and are particularly notable in some areas such as Sardinia. Haplogroup R1b frequencies vary from highs in western Europe in a steadily decreasing cline with growing distance from the Atlantic: 80-90% (Welsh, Basques, Irish, Scots, north-western Spanish, Portuguese and western French); around 40-60% in most other parts of western Europe. It drops outside this area and is around 20% or less in areas such as southern Italy, Sweden, Poland, Turkey, the Balkans and Cyprus. R1b remains the most common clade as one moves east to Germany, while further east in Poland, R1a is more common (see below). In southeastern Europe, R1b drops behind R1a in the area in and around Hungary and Serbia but is more common both to the south and north of this region. R1b in Western Europe is dominated by at least two sub-clades, R-U106, which is distributed from the east side of the Rhine into northern and central Europe (with a presence in England) and R-P312, which is most common west of the Rhine, including the British Isles.
Haplogroup I is found in the form of various sub-clades throughout Europe and is found at highest frequencies in Bosnia and Herzegovina, Croatia, Sweden, Norway, Sardinia, parts of Germany and other countries in the Balkan Peninsula and Scandinavia. This clade is only found in Europe and may have been there since before the LGM. Haplogroup R1a, almost entirely in the R1a1a sub-clade, is prevalent in much of central and eastern Europe (and also as far away as central Asia and the Indian subcontinent). For example there is a sharp increase in R1a1 and decrease in R1b1b2 as one goes east from Germany to Poland. and some small pockets in Southern Europe, for example the Pas Valley areas of Venice, and Calabria in Italy. In the Baltic countries R1a frequencies decrease from Lithuania (45%) to Estonia (around 30%).
Putting aside small enclaves there are also several haplogroups apart from the above three, which are most common in certain areas of Europe.
Haplogroup E1b1b1, mainly in the form of its E1b1b1a2 (E-V13) sub-clade reaches frequencies above 40% around the area of Kosovo. This clade is thought to have arrived in Europe from western Asia either in the later Mesolithic, or the Neolithic.
Haplogroup J, in various sub-clades is found in levels of around 15-30% in parts of the Balkans and Italy.
A similar study in 2007 using samples exclusively from Europe found that the most important genetic differentiation in Europe occurs on a line from the north to the south-east (northern Europe to the Balkans), with another east-west axis of differentiation across Europe. Its findings were consistent with earlier results based on mtDNA and Y-chromosonal DNA that support the theory that modern Iberians (Spanish and Portuguese) hold the most ancient European genetic ancestry, as well as separating Basques and Sami from other European populations. It suggested that the English and Irish cluster with other Northern and Eastern Europeans such as Germans and Poles, while some Basque and Italian individuals also clustered with Northern Europeans. Despite these stratifications, it noted the unusually high degree of European homogeneity: "there is low apparent diversity in Europe with the entire continent-wide samples only marginally more dispersed than single population samples elsewhere in the world."
In 2008, two international research teams published analyses of large-scale genotyping of large samples of Europeans, using over 300,000 autosomal SNPs. With the exception of usual isolates such as Basques, Finns and Sardinians, the European population lacked sharp discontinuities (clustering) as previous studies have found (see Seldin ''et al.'' 2006 and Bauchett ''et al.'' 2007), although there was a discernible south to north gradient. Overall, they found only a low level of genetic differentiation between subpopulations, and differences which did exist were characterized by a strong continent-wide correlation between geographic and genetic distance. In addition, they found that diversity was greatest in southern Europe due a larger effective population size and/or population expansion from southern to northern Europe. The researchers take this observation to imply that genetically, Europeans are not distributed into discrete populations.
A study in May 2009 of 19 populations from Europe using 270,000 SNPs highlighted the genetic diversity or European populations corresponding to the northwest to southeast gradient and distinguished "four several distinct regions" within Europe:
In this study, barrier analysis revealed "genetic barriers" between Finland, Italy and other countries and interestingly, barriers could also be demonstrated within Finland (between Helsinki and Kuusamo) and Italy (between northern and southern part, Fst= 0.0050). Fst (Fixation index) was found to correlate considerably with geographic distances ranging from ≤0.0010 for neighbouring populations to 0.0200-0.0230 for Southern Italy and Finland. For comparisons, pair-wise Fst of non-European samples were as follows: Europeans – Africans (Yoruba) 0.1530; Europeans – Chinese 0.1100; Africans (Yoruba) – Chinese 0.1900.
A study by Chao Tian in August 2009 extended the analysis of European population genetic structure to include additional southern European groups and Arab populations (Palestinians, Druzes...) from the Near-East. This study determined autosomal Fst between 18 population groups and concluded that, in general, genetic distances corresponded to geographical relationships with smaller values between population groups with origins in neighboring countries/regions (for example, Greeks/Tuscans: Fst = 0.0010, Greeks/Palestinians: Fst = 0.0057) compared with those from very different regions in Europe (for example Greeks/Swedish: Fst = 0.0087, Greeks/Russians: Fst = 0.0108).
+ Intercontinental autosomal genetic distances based on SNPs | |||
Europe (CEU) | Sub-Saharan Africa (Yoruba) | East-Asia (Chinese) | |
Europe (CEU) | 0.1530 | 0.1100 | |
Sub-Saharan Africa (Yoruba) | 0.1530 | 0.1900 | |
East-Asia (Chinese) | 0.1100 | 0.1900 |
+ Intra-European/mediterranean autosomal genetic distances based on SNPs | |||||||||
Italians | Palestinians | Swedish | Finns | Spanish | Germans | Russians | French | Greeks | |
Italians | 0.0064 | 0.0064-0.0090 | 0.0130-0.0230 | 0.0010-0.0050 | 0.0029-0.0080 | 0.0088-0.0120 | 0.0030-0.0050 | 0.0000 | |
Palestinians | 0.0064 | 0.0191 | 0.0101 | 0.0136 | 0.0202 | 0.0057 | |||
Swedish | 0.0064-0.0090 | 0.0191 | 0.0050-0.0110 | 0.0040-0055 | 0.0007-0.0010 | 0.0030-0.0036 | 0.0020 | 0.0084 | |
Finns | 0.0130-0.0230 | 0.0050-0.0110 | 0.0110-0.0170 | 0.0060-0.0130 | 0.0060-0.0120 | 0.0080-0.0150 | |||
Spanish | 0.0010-0.0050 | 0.0101 | 0.0040-0055 | 0.0110-0.0170 | 0.0015-0.0030 | 0.0070-0.0079 | 0.0010 | 0.0035 | |
Germans | 0.0029-0.0080 | 0.0136 | 0.0007-0.0010 | 0.0060-0.0130 | 0.0015-0.0030 | 0.0030-0.0037 | 0.0010 | 0.0039 | |
Russians | 0.0088-0.0120 | 0.0202 | 0.0030-0.0036 | 0.0060-0.0120 | 0.0070-0.0079 | 0.0030-0.0037 | 0.0050 | 0.0108 | |
French | 0.0030-0.0050 | 0.0020 | 0.0080-0.0150 | 0.0010 | 0.0010 | 0.0050 | |||
Greeks | 0.0000 | 0.0057 | 0.0084 | 0.0035 | 0.0039 | 0.0108 |
''Homo neanderthalensis'' inhabited much of Europe and western Asia from as far back as 130,000 years ago. They existed in Europe as late as 30,000 years ago. They were replaced by anatomically modern humans (A.M.H.), Cro-Magnoid ''Homo sapiens'', who began to appear in Europe c. 40,000 years ago. Given that the two hominid species likely co-existed in Europe, anthropologists wondered whether the two interacted. Before the advent of genetic studies, some anthropologists believed they had discovered skeletons representing Neanderthal-modern human 'hybrids'. These results were deemed 'ambiguous'. Archaeological evidence points to an abrupt change from Neanderthal artefacts to those related to A.M.H. during the Upper Palaeolithic. Y chromosomal and mtDNA data suggest that modern European DNA derives from Africa, which diverged less than 100,000 years ago, whereas the last common ancestor between the two species lived between 500,000 to 600,000 years ago. While it is conceivable that the autosomes of modern Europeans may retain Neanderthal sequences, Neanderthals were replaced by modern humans. Technological, economic and intellectual advantages not only allowed AMH to better adapt to the Upper Palaeolithic environment of Europe but probably also resulted in cultural and therefore biological barriers between the two species.
There has been speculation about the inheritance of specific genes from Neanderthals. For example one MAPT locus 17q21.3 which is split into deep genetic lineages H1 and H2. Since the H2 lineage seems restricted to European populations, several authors have suggested inheritance from Neanderthals. However the preliminary results from the sequencing of the full Neanderthal Genome have shown no evidence of interbreeding between Neanderthals and modern humans.
The latest findings by Paabo, Richard E. Green of the University of California, Santa Cruz and David Reich of Harvard Medical School, comparing the genetic material from the bones of three Neanderthals with that from five modern humans, show a relationship between Neanderthals and modern people outside Africa. This suggests that interbreeding occurred in the Middle East.
It is thought that modern humans began to colonize Europe during the Upper Paleolithic about 40,000 years ago. Some evidence shows the spread of the Aurignacian culture. From a Y-chromosome perspective, Semino proposed that the large haplogroup R1 is an ancient Eurasiatic marker brought in by ''Homo sapiens'' who diffused west into Europe ~ 40 ky ago. Haplogroup I might represent another putative Palaeolithic marker whose age has been estimated to ~ 22 kYa. Whilst it is 'unique' to Europe, it probably arose in descendants of men arriving from the Middle East c. 20 - 25 kYa, arising from parent haplogroup IJ. At this time, another Upper Palaeolithic culture appears, the Gravettian culture. Thus the genetic data suggests that, from a male perspective, modern humans might have taken two colonising routes, one from the middle east via the Balkans and another from Central Asia to the north of the Black Sea.
Martin Richards ''et al.'' found that 15 - 40% of extant mtDNA lineages trace back to the Palaeolithic migrations (depending on whether one allows for multiple founder events). Haplogroup H accounts for about half the gene lines in Europe, with many subgroups. The above mtDNA lineages or their precursors, are most likely to have arrived into Europe via the Middle East. This contrasts with Y DNA evidence, whereby some 50%+ of male lineages are characterized by the R1 superfamily, which is of possible central Asian origin. Semino postulates that these differences "may be due in part to the apparent more recent molecular age of Y chromosomes relative to other loci, suggesting more rapid replacement of previous Y chromosomes. Gender-based differential migratory demographic behaviors will also influence the observed patterns of mtDNA and Y variation".
About 25,000 years ago the most recent very cold period (the Last Glacial Maximum, LGM) began, rendering much of Europe uninhabitable. According to the classical model much of northern and central Europe was vacated and people took refuge in climatic sanctuaries (or refugia) as follows:
This event decreased the overall genetic diversity in Europe, a "result of drift, consistent with an inferred population bottleneck during the Last Glacial Maximum". As the glaciers receded from about 16,000-13,000 years ago, Europe began to be slowly repopulated by people from refugia, leaving genetic signatures.
Some Y haplogroup I clades appear to have diverged from their parental haplogroups sometime during or shortly after the LGM. Haplogroup I2 is prevalent in the western Balkans, as well as the rest of southeastern and central-eastern Europe in more moderate frequencies. Its frequency drops rapidly in central Europe, suggesting that the survivors bearing I2 lineages expanded predominantly through south-eastern and central-eastern Europe.
Cinnioglu sees evidence for the existence of an Anatolian refuge, which also harboured Hg R1b1b2. Today, R1b dominates the y chromosome landscape of western Europe and the British Isles, suggesting that there could have been large population composition changes based on migrations after the LGM.
Semino, Passarino and Pericic place the origins of haplogroup R1a within the Ukrainian ice-age refuge. Its current distribution in eastern Europe and parts of Scandinavia are in part reflective of a re-peopling of Europe from the southern Russian/Ukrainian steppes during the Late Glacial Maximum.
From an mtDNA perspective, Richards ''et al.'' found that the majority of mtDNA diversity in Europe is accounted for by post-glacial re-expansions during the late upper Palaeolithic/ Mesolithic. "The regional analyses lend some support to the suggestion that much of western and central Europe was repopulated largely from the southwest when the climate improved. The lineages involved include much of the most common haplogroup, H, as well as much of K, T, W, and X." The study could not determine whether there were new migrations of mtDNA lineages from the near east during this period; a significant input was deemed unlikely. The alternative model of more refugees was discussed by Bilton et al.
The duration of the Neolithic varied from place to place, starting with the introduction of farming and ending with the introduction of bronze implements. In SE Europe it was approximately 7000-3000 BC while in NW Europe 4500-1700 BC. During this era, the ''Neolithic revolution'' led to drastic economic as well as socio-cultural changes in Europe and this is also thought to have had a big effect on Europe's genetic diversity, especially concerning genetic lineages entering Europe from the Middle East into the Balkans. There were several phases of this period: In a late European Mesolithic prelude to the Neolithic it appears that Near Eastern peoples from areas which already had farming and who also had sea-faring technology, had a transient presence in Greece, for example at Franchthi Cave. There is consensus that agricultural technology and the main breeds of animals and plants which are farmed entered Europe from somewhere in the area of the Fertile Crescent and specifically the Levant region from the Sinai to Southern Anatolia (Less certainly, this agricultural revolution is sometimes argued to have in turn been partly triggered by movements of people and technology coming across the Sinai from Africa.)
An important issue regarding the genetic impact of neolithic technologies in Europe is the manner by which they were transferred into Europe; whether farming was introduced by a significant migration of farmers from the Near East (Cavalli-Sforza's biological ''demic diffusion'' model) or a "cultural diffusion" or a combination of the two. Secondarily, population geneticists have tried to clarify whether any genetic signatures of Near Eastern origin correspond to the expansion routes postulated by the archaeological evidence.
Martin Richards estimated that 11% of European mtDNA is due to immigration in this period. Gene flow from SE to NW Europe seems to have continued in the Neolithic, the percentage significantly declining towards the British Isles. Classical genetics also suggested that the largest admixture to the European Paleolithic/Mesolithic stock was due to the Neolithic revolution of the 7th to 5th millennia BC. Three main mtDNA gene groups have been identified as contributing Neolithic entrants into Europe: J, T1 and U3 (in that order of importance). With others they amount up to around 20% of the gene pool.In 2000, Semino's study on Y DNA revealed the presence of haplotypes belonging to the large clade E1b1b1 (E-M35). These were predominantly found in the southern Balkans, southern Italy and parts of Iberia. Semino connected this pattern, along with J haplogroup subclades, to be the Y-DNA component of Cavalli-Sforza's Neolithic demic-diffusion of farmers from the Near East. Rosser et al. rather saw it as a (direct) 'North African component' in European genealogy, although they did not propose a timing and mechanism to account for it. also described E1b1b as representing a late-Pleistocene migration from Africa to Europe over the Sinai Peninsula in Egypt, evidence for which does not show up in mitochondrial DNA.
Concerning timing the distribution and diversity of V13 however, proposed an earlier movement whereby the E-M78* lineage ancestral to all modern E-V13 men moved rapidly out of a Southern Egyptian homeland and arrived in Europe with only Mesolithic technologies. They then suggest that the E-V13 sub-clade of E-M78 only expanded subsequently as native Balkan 'foragers-cum-farmers' adopted Neolithic technologies from the Near East. They propose that the first major dispersal of E-V13 from the Balkans may have been in the direction of the Adriatic Sea with the Neolithic Impressed Ware culture often referred to as ''Impressa'' or Cardial. , rather propose that the main route of E-V13 spread was along the Vardar-Morava-Danube river 'highway' system.
In contrast to Battaglia, suggest (i) a different point of V-13 origin and (ii) a later dispersal time. Cruciani argues that V-13 arose in western Asia, where it is found in low but significant frequencies, from whence it entered the Balkans sometime after 11 kYa. It later experienced a rapid dispersal which he dated to c. 5300 years ago in Europe, coinciding with the Balkan Bronze Age. Like Peričic et al. they consider that "the dispersion of the E-V13 and J-M12 haplogroups seems to have mainly followed the river waterways connecting the southern Balkans to north-central Europe".
Most likely, the demographic history of V13 is complex, as later population movements further amplified it's frequency in the Europe. (See below.)
After an initial focus upon E1b1b as a Neolithic marker, a more recent study in January 2010, looked at Y haplogroup R1b1b, which is much more common in Western Europe. Mark Jobling said: "We focused on the commonest Y-chromosome lineage in Europe, carried by about 110 million men, it follows a gradient from south-east to north-west, reaching almost 100% frequency in Ireland. We looked at how the lineage is distributed, how diverse it is in different parts of Europe, and how old it is." The results suggested that the lineage R1b1b2 (R-M269), like E1b1b or J lineages, spread together with farming from the Near East. Dr Patricia Balaresque added: "In total, this means that more than 80% of European Y chromosomes descend from incoming farmers. In contrast, most maternal genetic lineages seem to descend from hunter-gatherers. To us, this suggests a reproductive advantage for farming males over indigenous hunter-gatherer males during the switch from hunting and gathering, to farming".
A more recent article concerning R1b made the counter claim that "the data are still controversial and the analyses so far performed are prone to a number of biases" and presented some evidence that R1b was also part of "an earlier, pre-Neolithic dispersal of haplogroups from a common ancestral gene pool".
The Bronze Age saw the development of long-distance trading networks, particularly along the Atlantic Coast and in the Danube valley. There was migration from Norway to Orkney and Shetland in this period (and to a lesser extent to mainland Scotland and Ireland). There was also migration from Germany to eastern England. Martin Richards estimated that there was about 4% mtDNA immigration to Europe in the Bronze Age.
One theory about the origin of the Indo-European language centres around a hypothetical Proto-Indo-European people, who are traced, in the Kurgan hypothesis, to somewhere north of the Black Sea at about 4500 BC. They domesticated the horse, and are considered to have spread their culture and genes across Europe. It has been difficult to identify what these "Kurgan" genes might be, though the Y haplogroup R1a is a proposed marker which would indicate that the physical expansion halted in Germany and only the Kurgan culture and language went farther. Another hypothesis — the Anatolian hypothesis — suggests an origin in Anatolia with a later expansion from eastern Europe.
To what extent Indo-European migrations replaced the indigenous Mesolithic peoples is debated.
During the Iron Age, Celts are recorded as having moved from Gaul into northern Italy, Eastern Europe and Anatolia. The relationship between the Celts of Gaul and Spain is unclear as any migration occurred before records exist.
Steven Bird has speculated that E1b1b1a was spread during the Roman era from Italy and the Balkans into the rest of Europe.
Concerning the late Roman period of Germanic "''Volkswanderung''", some suggestions have been made, at least for Britain, with Y haplogroup I1a being associated with Anglo-Saxon immigration in eastern England, and R1a being associated with Norse immigration in northern Scotland.
Category:Europe Demographics of Europe Europe Europe Europe Europe Category:European people Europe
eu:Europako historia genetikoa it:Storia genetica dell'EuropaThis text is licensed under the Creative Commons CC-BY-SA License. This text was originally published on Wikipedia and was developed by the Wikipedia community.
Name | Nigel Farage |
---|---|
Honorific-suffix | MEP |
Office | Europe of Freedom and Democracy President |
Term start | 1 July 2009 (de facto) |
Predecessor | (post established) |
Office | Leader of the United Kingdom Independence Party |
Term start | 5 November 2010 |
Predecessor | Jeffrey Titford |
Term start1 | 27 September 2006 |
Term end1 | 27 November 2009 |
Predecessor1 | Roger Knapman |
Successor1 | Lord Pearson of Rannoch |
Constituency mp2 | South East England |
Parliament2 | European |
Term start2 | 15 July 1999 |
Birth date | April 03, 1964 |
Birth place | Kent, England, United Kingdom |
Nationality | British |
Party | UK Independence Party |
Spouse | Gráinne Hayes (1988-?, divorced)Kirsten Mehr (1999-present) |
Children | 4 |
Alma mater | Dulwich College |
Website | Nigel Farage MEP |
Footnotes | }} |
Farage was a founding member of the UKIP, having left the Conservative Party in 1992 after they signed the Maastricht Treaty. Having unsuccessfully campaigned in European and Westminster parliamentary elections for UKIP since 1994, he gained a seat as an MEP for South East England in the 1999 European Parliament Election — the first year the regional list system was used — and was re-elected in 2004 and 2009. Farage describes himself as a libertarian and rejects the notion that he is a conservative.
In September 2006, Farage became the UKIP Leader and led the party through the 2009 European Parliament Election in which it received the second highest share of the popular vote, defeating Labour and the Liberal Democrats with over two million votes. However he stepped down in November 2009 to concentrate on contesting the Speaker John Bercow's seat of Buckingham in the 2010 general election.
At the 2010 General Election, Farage failed to unseat John Bercow and received only the third highest share of the vote in the constituency. Shortly after the polls opened on 6 May 2010, Nigel Farage was injured in an aircraft crash in Northamptonshire. The two-seated PZL-104 Wilga 35A had been towing a pro-UKIP banner when it flipped over and crashed shortly after takeoff. Both Farage and the pilot were hospitalised with non-life-threatening injuries.
In November 2010, Farage successfully stood in the 2010 UKIP leadership contest, following the resignation of its leader, Lord Pearson of Rannoch. Farage was also ranked 41st (out of 100) in ''The Daily Telegraph'''s Top 100 most influential right-wingers poll in October 2009, citing his media savvy and his success with UKIP in the European Elections. Farage was ranked 58th in the 2010 list compiled by Iain Dale and Brian Brivati for the Daily Telegraph.
Farage has been married twice. He married Gráinne Hayes in 1988, with whom he had two children: Samuel (1989) and Thomas (1991). In 1999 he married Kirsten Mehr, a German national, by whom he has two more children, Victoria (born 2000) and Isabelle (born 2005).
Farage has also penned his own memoirs, entitled "Fighting Bull." It outlines the founding of UKIP and his personal and political life so far.
He was elected to the European Parliament in 1999 and re-elected in 2004 and 2009. Farage is presently the leader of the thirteen-member UKIP contingent in the European Parliament, and co-leader of the multinational eurosceptic group, Europe of Freedom and Democracy.
At his maiden speech to the UKIP conference on 8 October 2006, he told delegates that the party was "at the centre-ground of British public opinion" and the "real voice of opposition". Farage said: "We've got three social democratic parties in Britain — Labour, Lib Dem and Conservative are virtually indistinguishable from each other on nearly all the main issues" and "you can't put a cigarette paper between them and that is why there are nine million people who don't vote now in general elections that did back in 1992."
At 10pm on 19 October 2006, Farage took part in a three-hour live interview and phone-in with James Whale on national radio station talkSPORT. Four days later, Whale announced on his show his intention to stand as UKIP's candidate in the 2008 London Mayoral Election. Farage said that Whale "not only has guts, but an understanding of what real people think". However Whale later decided not to stand and UKIP was represented by Gerard Batten. He stood again for UKIP leadership in 2010 after his successor Lord Pearson stood down. On the 5th November 2010 it was announced Farage had won the leadership contest.
When he contested the Bromley & Chislehurst constituency in a May 2006 by-election, organised after the sitting MP representing it, eurosceptic Conservative Eric Forth, died, Farage came third, winning 8% of the vote, beating the Labour Party candidate. This was the second-best by-election result recorded by UKIP out of 25 results, and the first time since the Liverpool Walton by-election in 1991 that a party in government had been pushed into fourth place in a parliamentary by-election on mainland Britain.
He stood against Buckingham MP John Bercow, the newly elected Speaker of the House of Commons, despite a convention that the speaker, as a political neutral, is not normally challenged in his or her bid for re-election by any of the major parties.
On 6 May, on the morning the polls opened in the election, just before eight o'clock Farage was involved in a light aircraft crash, suffering injuries described as non-life-threatening. A spokesperson told the BBC that "it was unlikely Mr Farage would be discharged from hospital today [6 May] Although his injuries were originally described as minor, his sternum and ribs were broken, and his lung punctured. The Air Accident Investigation Branch (AAIB) report said that the aeroplane was towing a banner, which caught in the tailplane, forcing the nose down.
Farage came third with 8,401 votes. Bercow was re-elected, and John Stevens, a former Conservative MEP (Defected to Lib-Dems), who campaigned with "Flipper the Dolphin" (a reference to MPs flipping second homes) came second with 10,331.
On 1 December 2010, the pilot of the aircraft involved in the accident was charged with threatening to kill Farage. He was also charged with threatening to kill an AAIB official involved in the investigation into the accident. In April 2011, Justin Adams was found guilty of making death threats. The judge said the defendant was "clearly extremely disturbed" at the time the offences happened adding "He is a man who does need help. If I can find a way of giving him help I will."
The former Europe Minister, Denis MacShane, said that this showed that Farage was "happy to line his pockets with gold". Farage called this a "misrepresentation", pointing out that the money had been used to promote UKIP's message, not salary, but he welcomed the focus on the issue of MEP expenses, claiming that "[o]ver a five year term each and every one of Britain's 78 MEPs gets about £1 million. It is used to employ administrative staff, run their offices and to travel back and forth between their home, Brussels and Strasbourg." He also pointed out the money spent on the YES campaign in Ireland by the European Commission was "something around 440 million", making the NO campaign's figure insignificant in comparison.
Farage persuaded around 75 MEPs from across the political divide to back a motion of no confidence in Barroso, which would be sufficient to compel Barroso to appear before the European Parliament to be questioned on the issue. The motion was successfully tabled on 12 May 2005, and Barroso appeared before Parliament at a debate on 26 May 2005. The motion was heavily defeated. A Conservative MEP, Roger Helmer, was expelled from his group, the European People's Party - European Democrats (EPP-ED) in the middle of the debate by that group's leader Hans-Gert Poettering as a result of his support for Farage's motion.
Category:1964 births Category:Living people Category:United Kingdom Independence Party politicians Category:Members of the European Parliament for English constituencies Category:Critics of the European Union Category:People from Farnborough, London Category:Old Alleynians Category:Leaders of the United Kingdom Independence Party Category:British libertarians Category:UK Independence Party MEPs Category:MEPs for the United Kingdom 1999–2004 Category:MEPs for the United Kingdom 2004–2009 Category:MEPs for the United Kingdom 2009–2014
br:Nigel Farage cs:Nigel Farage cy:Nigel Farage de:Nigel Farage et:Nigel Farage es:Nigel Farage fr:Nigel Farage it:Nigel Farage nl:Nigel Farage pl:Nigel Farage ro:Nigel Farage simple:Nigel Farage fi:Nigel Farage sv:Nigel FarageThis text is licensed under the Creative Commons CC-BY-SA License. This text was originally published on Wikipedia and was developed by the Wikipedia community.
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