History of Italy |
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Italyportal |
This section may be too technical for most readers to understand.(January 2025) |
The genetic history of Italy includes information around the formation, ethnogenesis, and other DNA-specific information about the inhabitants of Italy. Modern Italians mostly descend from the ancient peoples of Italy, including Indo-European speakers (Romans and other Latins, Falisci, Picentes, Umbrians, Samnites, Oscans, Sicels, Elymians, Messapians and Adriatic Veneti, as well as Magno-Greeks, Cisalpine Gauls and Illyric Iapygians) and pre-Indo-European speakers (Etruscans, Ligures, Rhaetians Camunni, Sicani, Nuragic peoples), as well as settlers from Phoenicia and Carthage in Sardinia and in the westernmost part of Sicily. Other groups migrated into Italy as a result of the Roman Empire, when the Italian peninsula attracted people from the various regions of the empire (North Africa, West Asia and the rest of Europe), [2] and during the Middle Ages with the arrival of Ostrogoths, Longobards, Franks, Saracens and Normans among others. Based on DNA analysis, there is evidence of regional genetic substructure and continuity within modern Italy dating back to antiquity. [3] [4] [5] [6]
In their admixture ratios, Italians are similar to other Southern Europeans, and that is being of primarily Neolithic Early European Farmer ancestry, along with smaller, but still significant, amounts of Mesolithic Western Hunter-Gatherer, Bronze Age Steppe pastoralist (Indo-European speakers) and Chalcolithic or Bronze Age Iranian/Caucasus-related ancestry. [4] [7] [8] [9] [10] [4] According to multiple genome-wide studies Southern Italians are closest to modern Greeks, [11] [12] [13] [14] [15] [16] [17] [18] [19] [10] while Northern Italians are closest to the Spaniards, the Portuguese and to a lesser extent people from Southern France. [11] [18] [20] [21] [22] [17] [23] [24] [25] [26] [19] [27] There is also Bronze/Iron Age Anatolian admixture in Italy, with a much lower incidence in Northern Italy compared with Central Italy and Southern Italy. [24] [8] Marginal levels (0.1-4%) of North African admixture is also found in Southern Italy with the highest incidence being in the islands of Sicily and Sardinia. [24] [8] [4]
Latin samples from Latium in the Iron Age and early Roman Republican period were generally found to genetically cluster closest to modern Northern and Central Italians (four out of six were closest to Northern and Central Italians, while the other two were closest to Southern Italians). [28] DNA analysis demonstrates that ancient Greek colonization had a significant lasting effect on the local genetic landscape of Southern Italy and Sicily ( Magna Graecia ), with modern people from that region having significant Greek admixture. [29] [14] Overall, the genetic differentiation between the Latins, Etruscans and the preceding proto-Villanovan population of Italy was found to be insignificant. [30] In 2019, aDNA analysis of Roman fossils detected substantial genetic ancestry shift towards central and northern European ancestry in the inhabitants of the city of Rome in late antiquity and the medieval era. The authors tentatively link the origin of this ancestry with Visigoths and Lombards. Previously, most citizens in the imperial era clustered with central and east Mediterranean peoples, such as central and south Italians, Greeks, Cypriots and Maltese, and to some extent, Levantine and Near Eastern peoples. This was caused by direct immigration and contact with Greek, Phoenician and Punic diasporas. [2] [31] A 2020 analysis of maternal haplogroups from ancient and modern samples indicates a substantial genetic similarity and continuity between the modern inhabitants of Umbria in central Italy and ancient inhabitants of the region belonging to the Italic-speaking Umbrian culture. [6]
Multiple DNA studies confirmed that genetic variation in Italy is clinal, going from the Eastern to the Western Mediterranean. The Sardinians are the exception as genetic outliers in Italy and indeed in Europe, resulting from their predominantly Neolithic, Pre-Indo-European and non-Italic Nuragic ancestry. [32] [7] [8] [9] Reflecting the history of Europe and the broader Mediterranean basin, the Italian populations have been found to be made up mostly of the same ancestral components, albeit in different proportions, from the Mesolithic, Neolithic and Bronze Age settlements of Europe. [24] [21] [33]
The genetic gap between northern and southern Italians is filled by an intermediate Central Italian cluster, creating a continuous cline of variation that mirrors geography. [25] The only exceptions are some minority populations (mostly Slovene minorities from the region of Friuli-Venezia Giulia) who cluster with the Slavic-speaking Central Europeans in Slovenia, [34] as well as the Sardinians, who are clearly differentiated from the populations of both mainland Italy and Sicily. [21] [4] A study on some linguistic and isolated communities residing in Italy revealed that their genetic diversity at short (0–200 km) and intermediate distances (700–800 km) was greater than that observed throughout the entire European continent. [5]
The genetic distance between Northern and Southern Italians, although large for a single European nationality, is similar to that between the Northern and the Southern Germans. [35] Northern and Southern Italians began to diverge as early as the Late Glacial, and appear to encapsulate at a smaller scale the cline of genetic diversity observable across Europe. [36]
Modern humans appeared during the Upper Paleolithic. Specimens of Aurignacian age were discovered in the cave of Fumane and date back about 34,000 years. During the Magdalenian period, the first humans from the Pyrenees populated Sardinia. [37]
During the Neolithic period, farming was introduced by people from the east and the first villages were built. Weapons became more sophisticated and the first objects in clay were produced. In the late Neolithic era the use of copper spread, and villages were built over piles near lakes. In Sardinia, Sicily and a part of Mainland Italy the Beaker culture spread from Western and Central Europe. Sicily also suffered the influences of the Aegean in the Mycenaean period.
During the Late Bronze Age the Urnfield Proto-Villanovan culture appeared in Central and Northern Italy. It is characterized by the rite of cremation of dead bodies, which originated from Central Europe. The use of iron began to spread. [38] In Sardinia, the Nuragic civilization flourished.
At the dawn of the Iron Age much of Italy was inhabited by Italic tribes such as the Latins, Sabines, Samnites, and Umbrians. The Northwest and Alpine territories were populated primarily by pre-Indo European speakers such as the Etruscans, Ligurians, Camunni and Raetians; while Iapygian tribes, possibly of Illyrian origin, populated Apulia.
From the 8th century BC, Greek colonists settled on the southern Italian coast and founded cities, forming what would be later called Magna Graecia. Around the same time, Phoenician colonists settled on the western side of Sicily. During the same period the Etruscan civilization developed on the coast of Southern Tuscany and Northern Latium. In the 4th century BC, Gauls settled in Northern Italy and in parts of Central Italy. [39] With the fall of the Western Roman Empire, different populations of Germanic origin invaded Italy, the most significant being the Lombards, [40] followed five centuries later by the Normans in Sicily.
There have been a number of genetic studies of Etruscans and modern Tuscans compared with other populations, some of which indicate the local, European origin of Etruscans and others supportive of an origin from elsewhere. In general, the direct testing of ancient Etruscan DNA has supported a deep, local origin, while the testing of modern samples as a proxy for Etruscans is rather inconclusive and inconsistent. [41] [42]
The very large mtDNA study from 2013 indicates, based on maternally-inherited DNA from 30 bone samples taken from tombs dating from the eight century to the first century BC from Tuscany and Lazio, that the Etruscans were a native population. [43] [44] The study extracted and typed the hypervariable region of mitochondrial DNA of 14 individuals buried in two Etruscan necropoleis, analyzing them along with previously analyzed Etruscan mtDNA, other ancient European mtDNA, modern and Medieval samples from Tuscany, and 4,910 modern individuals from the Mediterranean basin. The ancient (30 Etruscans, 27 Medieval Tuscans) and modern DNA sequences (370 Tuscans) were subjected to several million computer simulation runs, showing that the Etruscans can be considered ancestral to Medieval and, especially in the subpopulations from Casentino and Volterra, of modern Tuscans; modern populations from Murlo and Florence, by contrast, were shown not to continue the Medieval population. By further considering two Anatolian samples (35 and 123 individuals), it was estimated that the genetic links between Tuscany and Anatolia date back to at least 5,000 years ago, and the "most likely separation time between Tuscany and Western Anatolia falls around 7,600 years ago", strongly suggesting that the Etruscan culture developed locally, and not as an immediate consequence of immigration from the Eastern Mediterranean shores. According to the study, ancient Etruscan mtDNA is closest among modern European populations and is not particularly close to Anatolian or other Eastern Mediterranean populations. Among ancient populations based on mtDNA, ancient Etruscans were found to be closest to LBK Neolithic farmers from Central Europe. [43] [44]
This result is largely in line with previous mtDNA results from 2004 (in a smaller study also based on ancient DNA), and contradictory to results from 2007 (based on modern DNA). The 2004 study was based on mitochondrial DNA (mtDNA) from 80 bone samples, reduced to 28 bone samples in the analysis phase, taken from tombs dating from the seventh century to the third century BC from Veneto, Tuscany, Lazio and Campania. [45] This study found that the ancient DNA extracted from the Etruscan remains had some affinities with modern European populations including Germans, English people from Cornwall, and Tuscans in Italy. In addition the Etruscan samples possibly revealed more genetic inheritance from the eastern and southern Mediterranean than modern Italian samples contain. The study was marred by concerns that mtDNA sequences from the archeological samples represented severely damaged or contaminated DNA; [46] however, subsequent investigation showed that the samples passed the most stringent tests of DNA degradation available. [47]
A mtDNA study, published in 2018 in the journal American Journal of Physical Anthropology, compared both ancient and modern samples from Tuscany, from the Prehistory, Etruscan age, Roman age, Renaissance, and Present-day, and concluded that the Etruscans appear as a local population, intermediate between the prehistoric and the other samples, placing in the temporal network between the Eneolithic Age and the Roman Age. [48]
A 2019 genetic study published in the journal Science analyzed the remains of eleven Iron Age individuals from the areas around Rome, of which four were Etruscan individuals, one buried in Veio Grotta Gramiccia from the Villanovan period (900-800 BC) and three buried in La Mattonara Necropolis near Civitavecchia from the Orientalizing period (700-600 BC). The study concluded that Etruscans (900–600 BC) and the Latins (900–500 BC) from Latium vetus were genetically similar., [49] genetic differences between the examined Etruscans and Latins were found to be insignificant. [50] The Etruscan individuals and contemporary Latins were distinguished from preceding populations of Italy by the presence of 30.7% steppe ancestry. [51] Their DNA was a mixture of two-thirds Copper Age ancestry (EEF + WHG; Etruscans ~66–72%, Latins ~62–75%) and one-third Steppe-related ancestry (Etruscans ~27–33%, Latins ~24–37%) (with the EEF component mainly deriving from Neolithic-era migrants to Europe from Anatolia and the WHG being local Western European hunter-gatherers, with both components, along with that from the steppe, being found in virtually all European populations). [49] The only sample of Y-DNA extracted belonged to haplogroup J-M12 (J2b-L283), found in an individual dated 700-600 BC, and carried exactly the M314 derived allele also found in a Middle Bronze Age individual from Croatia (1631-1531 calBCE). While the four samples of mtDNA extracted belonged to haplogroups U5a1, H, T2b32, K1a4. [52] Therefore, Etruscans had also Steppe-related ancestry despite speaking a pre-Indo-European language.
A 2021 study by the Max Planck Institute, the Universities of Tübingen, Florence, and Harvard, published in the journal Science Advances, analyzed the Y-chromosome, mitochondrial DNA, and autosomal DNA of 82 ancient samples from Etruria (Tuscany and Latium) and southern Italy (Basilicata) spanning from 800 BC to 1000 AD, including 48 Iron Age individuals. The study confirmed that in the samples of Etruscan individuals from Tuscany and Lazio the ancestral component Steppe was present in the same percentages found in the previously analyzed samples of Iron Age Latins, and added that in the DNA of the Etruscans was completely absent, a signal of recent admixture with Anatolia or the Eastern Mediterranean. The study concluded that the Etruscans were autochthonous and they had a genetic profile similar to that of their early Iron Age Latin neighbors. Both Etruscans and Latins belonged firmly to the European cluster: 75% of the samples of Etruscan male individuals were found to belong to haplogroup R1b, especially R1b-P312 and its derivative R1b-L2 whose direct ancestor is R1b-U152. Regarding mitochondrial DNA haplogroups, the most prevalent was largely H, followed by J and T. Uniparental marker data and autosomal DNA data from samples of Iron Age Etruscan individuals suggest that Etruria received migrations with a large ancestral Steppe component during the 2nd millennium BC, related to the spread of Indo-European languages, starting with the Bell Beaker culture, and that these migrations merged with populations of the oldest pre-Indo-European layer present since at least the Neolithic period, but it was the latter's language that survived, a situation similar to what happened in the Basque region of northern Spain. The study also concluded that the samples analyzed show that the Etruscans kept their genetic profile unchanged for almost 1000 years, indicating the sparse presence in Etruria of foreigners, and that a demographic change in Etruria occurred only from the Roman imperial period, in which there is the intermixture into the local population of ancestral components from the Eastern Mediterranean Sea. Analysis of samples of individuals who lived in the Roman imperial period and those of the Medieval Age also suggest that the genetic landscape of present-day central Italy was formed largely around 1000 years ago after the Barbarian invasions, and that the arrival of the Germanic Lombards in Italy contributed to the formation of the gene pool of the modern population of Tuscany and northern Latium. [53]
In 2024, 6 individuals of Etruscan remains from Tarquinia, Lazio, dated the 9th-7th Century BC, were studied and confirmed the previous finds. The admixture model showed that they were 84-92% Italy Bell Beaker and 8-26% additional Yamnaya Samara (Steppe-related) ancestry, but with one individual being more similar to Iron Age populations from Scandinavia, and north-west Europe. The two male individuals studied for Y-Chromosome belonged to the J2b/J-M12 lineage, and the five studied mitochondrial haplogroups were typical of post-Neolithic Europe. Phenotypic traits showed blue-eyes, light/dark brown hair, and pale to intermediate skin tones. [54]
An mtDNA study from 2007, by contrast, earlier suggested a Near Eastern origin. [55] Achilli et al. (2007) found in a modern sample of 86 individuals from Murlo, a small town in southern Tuscany, an unusually high frequency (17.5%) of supposed Near Eastern mtDNA haplogroups, while other Tuscan populations do not show the same striking feature. Based on this result Achilli concluded that "their data support the scenario of a post-Neolithic genetic input from the Near East to the present-day population of Tuscany, a scenario in agreement with the Lydian origin of Etruscans". This research has been much criticized by archeologists, etruscologists and classicists. [56] In the absence of any dating evidence, there is no direct link between this genetic input found in Murlo and the Etruscans. Furthermore, there is no evidence that these mtDNA haplogroups found in Murlo might be proof of an eastern origin of the Etruscans, as some of these mtDNA haplogroups have been found in other studies as early as the Neolithic and Aeneolithic in Italy and Germany. [48] All the mtDNA haplogroups found in the modern sample from Murlo and classified by Achilli et al. as of Near Eastern origin are actually widespread in modern samples from other areas of Italy and Europe with no link with the Etruscans. [57]
A recent Y-DNA study from 2018 on a modern sample of 113 individuals from Volterra, a town of Etruscan origin, Grugni at al. keeps all the possibilities open, although the autochthonous scenario is the most supported by numbers, and concludes that "the presence of J2a-M67* (2.7%) suggests contacts by sea with Anatolian people, the finding of the Central European lineage G2a-L497 (7.1%) at considerable frequency would rather support a Northern European origin of Etruscans, while the high incidence of European R1b lineages (R1b 49.8%, R1b-U152 24.5%) cannot rule out the scenario of an autochthonous process of formation of the Etruscan civilization from the preceding Villanovan society, as suggested by Dionysius of Halicarnassus". [58] In Italy Y-DNA J2a-M67*, not yet found in Etruscan samples, is more widespread on the Adriatic Sea coast between Marche and Abruzzo, and not in those where once lived the Etruscans, and in the study has its peak in the Ionian side of Calabria. [59] [60] In 2014, a late Bronze Age Kyjatice culture sample in Hungary was found to be J2a1-M67, [61] a couple of J2a1b were found in Late Neolithic samples from the LBK culture in Austria, [62] a J2a1a was found in a Middle Neolithic Sopot culture sample from Croatia, [62] a J2a was found in a Late Neolithic Lengyel Culture sample from Hungary. [63] In 2019, in a Stanford study published in Science, two ancient samples from the Neolithic settlement of Ripabianca di Monterado in the province of Ancona, in the Marche region of Italy, were found to be Y-DNA J-L26 and J-M304. [49] In 2021, two more ancient samples from the Chalcolitich settlement of Grotta La Sassa, in the province of Latina in southern Lazio, were found to be Y-DNA J2a7-Z2397. [64] Therefore, Y-DNA J2a-M67 is likely in Italy since the Neolithic and can't be the proof of recent contacts with Anatolia.
Recent studies on the population structure of modern-day Italians have shown that in Italy there is a north–south cline for Y-chromosome lineages and autosomal loci, with a clear differentiation of peninsular Italians from Sardinians, and that modern Tuscans are the population of central Italy closest genetically to the inhabitants of northern Italy. [65] A 2019 study, based on autosomal DNA of 1616 individuals from all 20 Italian administrative regions, concludes that Tuscans join the northern Italian cluster, close to the inhabitants of Liguria and Emilia-Romagna. [66] A 2013 study, based on uniparental markers of 884 unrelated individuals from 23 Italian locations, had shown that the structure observed for the paternal lineages in continental Italy and Sicily suggests a shared genetic background between people from Tuscany and Northern Italy from one side, and people from Southern Italy and the Adriatic coast from the other side. The most frequent Y-DNA haplogroups in the group represented by populations from North-Western Italy, including Tuscany and most of the Padana plain, are four R1b-lineages (R-U152*, R-M269*, R-P312* and R-L2*). [60]
In the collective volume Etruscology published in 2017, British archeologist Phil Perkins provides an analysis of the state of DNA studies and writes that "none of the DNA studies to date conclusively prove that Etruscans were an intrusive population in Italy that originated in the Eastern Mediterranean or Anatolia" and "there are indications that the evidence of DNA can support the theory that Etruscan people are autochthonous in central Italy". [42]
In his book A Short History of Humanity published in 2021, German geneticist Johannes Krause, co-director of the Max Planck Institute for Evolutionary Anthropology in Jena, concludes that it is likely that the Etruscan language (as well as Basque, Paleo-Sardinian and Minoan) "developed on the continent in the course of the Neolithic Revolution". [67]Many Italians, especially in Northern Italy and Central Italy, belong to Haplogroup R1b, common in Western and Central Europe. The highest frequency of R1b is found in Garfagnana (76.2%) in Tuscany and in the Bergamo Valleys (80.8%) in Lombardy. [68] [69] This percentage lowers in the south of Italy in Calabria (33.2%). [68] On the other hand 39% of the Sardinians belong to Mesolithic European haplogroup I2a1a. [70] [71]
A study from the Università Cattolica del Sacro Cuore found that while Greek colonization left little significant genetic contribution, data analysis sampling 12 sites in the Italian peninsula supported a male demic diffusion model and Neolithic admixture with Mesolithic inhabitants. [72] The results supported a distribution of genetic variation along a north–south axis and supported demic diffusion. South Italian samples clustered with southeast and south-central European samples, and northern groups with West Europe. [72] [73]
A 2004 study by Semino et al. showed that Italians from the north-central regions had around 26.9% J2; the Apulians, Calabrians and Sicilians had 29.1%, 21.5% and 16.7% J2 respectively; the Sardinians had 9.7% J2. [74]
A 2018 genetic study, focusing on the Y-chromosome and haplogroups lineages, their diversity and their distribution by taking some 817 representative subjects, gives credit to the traditional northern-southern division in population, by concluding that due to Neolithic migrations southern Italians "show a higher similarity with Middle Eastern and Southern Balkan populations than northern ones; conversely, northern samples are genetically closer to North-West Europe and Northern Balkan groups". The position of Volterra in central Tuscany keeps the debate about the origins of Etruscans open, although the numbers are strongly in favor of the autochthonous thesis: the low presence of J2a-M67* (2.7%) suggests contacts by sea with Anatolian people; the presence of Central European lineage G2a-L497 (7.1%) at considerable frequency would rather support a Central European origin of the Etruscans; and finally, the high incidence of European R1b lineages (R1b 50% approx., R1b-U152 24.5%) — especially of haplogroup R1b-U152 — could suggest an autochthonous origin due to a process of formation of the Etruscan civilisation from the preceding Villanovan culture, following the theories of Dionysius of Halicarnassus, [68] as already supported by archaeology, anthropology and linguistics. [75] [76] [77] [78] In 2019, in a Stanford study published in Science, two ancient samples from the Neolithic settlement of Ripabianca di Monterado in province of Ancona, in the Marche region of Italy, were found to be Y-DNA J-L26 and J-M304. [2] Therefore, Y-DNA J2a-M67, downstream to Y-DNA J-L26 and J-M304, is most likely in Italy since the Neolithic and can't be the proof of recent contacts with Anatolia.
In two villages in Lazio and Abruzzo (Cappadocia and Vallepietra), I1 is the most common Y-DNA, recorded at levels 35% and 28%. [79] In Sicily, further migrations from the Vandals and Saracens have only slightly affected the ethnic composition of the Sicilian people. However, specifically Greek genetic legacy is estimated at 37% in Sicily. [29]
The Norman conquest of southern Italy caused the Norman Kingdom of Sicily to be created in 1130, with Palermo as capital, 70 years after the initial Norman invasion and 40 after the conquest of the last town, Noto in 1091, and would last until 1198. Nowadays it is in central and western Sicily, that Norman Y-DNA is common, with 15% to 20% of the lineages belonging to haplogroup I, this percentage drops to 8% in the eastern part of the island. The North African male contribution to Sicily was estimated between 0% and 7.5%. [80] [14] [81] Overall, the estimated Southern Balkan and Western European paternal contributions in Sicily are about 63% and 26% respectively. [81]
A 2015 genetic study of six small mountain villages in eastern Lazio and one mountain community in nearby western Abruzzo found some genetic similarities between these communities and Near Eastern populations, mainly in the male genetic pool. The Y haplogroup Q, common in Western Asia and Central Asia, was also found among this sample population, suggesting that in the past could have hosted a settlement from Anatolia. [79] Also, it is about 0.6% in continental Italy, but it rises to 2.5% (6/236) in Sicily, where it reaches 16.7% (3/18) in Mazara del Vallo region, followed by 7.1% (2/28) in Ragusa, 3.6% in Sciacca, [29] and 3.7% in Belvedere Marittimo. [82]
In Italy as elsewhere in Europe the majority of mtDNA lineages belong to the haplogroup H. Several independent studies conclude that haplogroup H probably evolved in West Asia c. 25,000 years ago. It was carried to Europe by migrations c. 20–25,000 years ago, and spread with population of the southwest of the continent. [83] [84] Its arrival was roughly contemporary with the rise of the Gravettian culture. The spread of subclades H1, H3 and the sister haplogroup V reflect a second intra-European expansion from the Franco-Cantabrian region after the last glacial maximum, c. 13,000 years ago. [83] [85]
African Haplogroup L lineages are relatively infrequent (less than 1%) throughout Italy with the exception of Latium, Volterra, Basilicata and Sicily where frequencies between 2 and 3% have been found. [86]
A study in 2012 by Brisighelli et al. stated that an analysis of ancestral informative markers "as carried out in the present study indicated that Italy shows a very minor sub-Saharan African component that is, however, slightly higher than non-Mediterranean Europe." Discussing African mtDNAs the study states that these indicate that a significant proportion of these lineages could have arrived in Italy more than 10,000 years ago; therefore, their presence in Italy does not necessarily date to the time of the Roman Empire, the Atlantic slave trade or to modern migration." [33] These mtDNAs by Brisighelli et al. were reported with the given results as "Mitochondrial DNA haplotypes of African origin are mainly represented by haplogroups M1 (0.3%), U6 (0.8%) and L (1.2%) for the 583 samples tested. [33] The haplogroups M1 and U6 can be considered to be of North African origin and could therefore be used to signal the documented African historical input. Haplogroup M1 was observed in only two carriers from Trapani (West Sicily), while U6 was observed only in Lucera, South Apulia, and another at the tip of the Peninsula (Calabria). [33]
A 2013 study by Alessio Boattini et al. found 0 of African L haplogroup in the whole Italy out of 865 samples. The percentages for Berber M1 and U6 haplogroups were 0.46% and 0.35%, respectively. [87]
A 2014 study by Stefania Sarno et al. found 0 of African L and M1 haplogroups in mainland Southern Italy out of 115 samples. Only two Berber U6 out of 115 samples were found, one from Lecce and one from Cosenza. [81]
A close genetic similarity between Ashkenazim and Italians has been noted in genetic studies, possibly due to the fact that Ashkenazi Jews have a significant European admixture (30–60%), much of it Southern European, a lot of which came from Italy when Jewish diaspora males of Middle Eastern origin migrated to Rome and found wives among local women who then converted to Judaism. [88] [89] [90] [91] [92] [22] [93] More specifically, Ashkenazi Jews could be modeled as being 50% Levantine and 50% European, with an estimated mean South European admixture of 37.5%. Most of it (30.5%) seems to derive from an Italian source. [94] [95]
A 2010 study of Jewish genealogy found that with respect to non-Jewish European groups, the populations which are most closely related to Ashkenazi Jews are modern-day Italians followed by the French and Sardinians. [96] [97]
Recent studies have shown that Italy played an important role in the recovery of "Western Europe" at the end of the Last glacial period. The study which was focused on the mitochondrial U5b3 haplogroup discovered that this female lineage had in fact originated in Italy and around 10,000 years ago it expanded from the Peninsula towards Provence and the Balkans. In Provence, probably between 9,000 and 7,000 years ago, it gave rise to the haplogroup subclade U5b3a1. This subclade U5b3a1 later came from Provence to the island of Sardinia by way of obsidian merchants, because it is estimated that 80% of the obsidian which is found in France comes from Monte Arci in Sardinia, reflecting the close relationship which once existed between these two regions. Still about 4% of the female population of Sardinia belongs to this haplotype. [98]
A mtDNA study, published in 2018 in the journal American Journal of Physical Anthropology, compared both ancient and modern samples from Tuscany, from the Prehistory, Etruscan age, Roman age, Renaissance, and Present-day, and concluded that the Etruscans appear as a local population, intermediate between the prehistoric and the other samples, placing in the temporal network between the Eneolithic Age and the Roman Age. [99]
A 2020 analysis of maternal haplogroups from ancient and modern samples in the central Italian region of Umbria finds a substantial genetic similarity among modern Umbrians and the area's pre-Roman inhabitants, and evidence of substantial genetic continuity in the region from pre-Roman times to the present. Both modern and ancient Umbrians were found to have high rates of mtDNA haplogroups U4 and U5a, and an overrepresentation of J (at roughly 30%). The study also found that, "local genetic continuities are further attested to by six terminal branches (H1e1, J1c3, J2b1, U2e2a, U8b1b1 and K1a4a)" also shared by ancient and modern Umbrians. [6]
Wade et al. (2008) determined that Italy is one of the last two remaining genetic islands in Europe, the other being Finland. This is due in part to the presence of the Alpine mountain chain which, over the centuries, has prevented large migration flows. [101]
Recent genome-wide studies have been able to detect and quantify admixture like never before. Li et al. (2008), using more than 600,000 autosomal SNPs, identify seven global population clusters, including European, Middle Eastern and Central/South Asian. All the Italian samples belong to Central-Western group with minor influences dating to Neolithic period. [102]
López Herráez et al. (2009) typed the same samples at close to 1 million SNPs and analyzed them in a Western Eurasian context, identifying a number of subclusters. This time, all of the European samples show some minor admixture. Among the Italians, Tuscany still has the most, and Sardinia has a bit too, but so does Lombardy (Bergamo), which is even farther north. [103]
A 2011 study by Moorjani et al. found that many southern Europeans have inherited 1–3% Sub-Saharan ancestry, although the percentages were lower (0.2–2.1%) when reanalyzed with the 'STRUCTURE' statistical model. An average admixture date of around 55 generations/1100 years ago was also calculated, "consistent with North African gene flow at the end of the Roman Empire and subsequent Arab migrations" [104]
A 2012 study by Di Gaetano et al. used 1,014 Italians with wide geographical coverage. It showed that the current population of Sardinia can be clearly differentiated genetically from mainland Italy and Sicily, and that a certain degree of genetic differentiation is detectable within the current Italian peninsula population.
By using the ADMIXTURE software, the authors obtained at K = 4 the lowest cross-validation error. The HapMap CEU individuals showed an average Northern Europe (NE) ancestry of 83%. A similar pattern is observed in French, Northern Italian and Central Italian populations with a NE ancestry of 70%, 56% and 52% respectively. According to the PCA plot, also in the ADMIXTURE analysis there are relatively small differences in ancestry between Northern Italians and Central Italians while Southern Italians showed a lower average admixture NE proportion (44%) than Northern and Central Italy, and a higher Caucasian ancestry of 28%. The Sardinian samples display a pattern of crimson common to the others European populations but at a higher frequency (70%). The average admixture proportions for Northern European ancestry within current Sardinian population is 14.3% with some individuals exhibiting very low Northern European ancestry (less than 5% in 36 individuals on 268 accounting the 13% of the sample). [21]
A 2013 study by Peristera Paschou et al. confirms that the Mediterranean Sea has acted as a strong barrier to gene flow through geographic isolation following initial settlements. Samples from (Northern) Italy, Tuscany, Sicily and Sardinia are closest to other Southern Europeans from Iberia, the Balkans and Greece, who are in turn closest to the Neolithic migrants that spread farming throughout Europe, represented here by the Cappadocian sample from Anatolia. But there hasn't been any significant admixture from the Middle East or North Africa into Italy and the rest of Southern Europe since then. [17]
Ancient DNA analysis reveals that Ötzi the Iceman clusters with modern Southern Europeans and closest to Italians (the orange "Europe S" dots in the plots below), especially those from the island of Sardinia. Other Italians pull away toward Southeastern and Central Europe consistent with geography and some post-Neolithic gene flow from those areas (e.g. Italics, Greeks, Etruscans, Celts), but despite that and centuries of history, they're still very similar to their prehistoric ancestor. [105]
A 2013 study by Botigué et al. 2013 applied an unsupervised clustering algorithm, ADMIXTURE, to estimate allele-based sharing between Africans and Europeans. Regarding Italians, the North African ancestry does not exceed 2% of their genomes. On average, 1% of Jewish ancestry is found in Tuscan HapMap population and Italian Swiss, as well as Greeks and Cypriots. Contrary to past observations, Sub-Saharan ancestry is detected at <1% in Europe, with the exception of the Canary Islands. [81]
Haak et al. (2015) conducted a genome wide study of 94 ancient skeletons from Europe and Russia. The study argues that Bronze Age steppe pastoralists from the Yamna culture spread Indo-European languages in Europe. Autosomic tests indicate that the Yamnaya-people were the result of admixture between two different hunter-gatherer populations: Eastern Hunter-Gatherers from the Russian Steppe and either Caucasus Hunter-Gatherers or Chalcolithic Iranians (who are very similar). Wolfgang Haak estimated a 27% ancestral contribution of the Yamnaya in the DNA of modern Tuscans, a 25% ancestral contribution of the Yamnaya in the DNA of modern Northern Italians from Bergamo, excluding Sardinians (7%), and to a lesser extent Sicilians (12%). [20]
A 2016 study Sazzini et al., confirms the results of previous studies by Di Gaetano et al. (2012) and Fiorito et al. (2015) but has much better geographical coverage of samples, with 737 individuals from 20 locations in 15 different regions being tested. The study also for the first time includes a formal admixture test that models the ancestry of Italians by inferring admixture events using all of the Western Eurasian samples. The results are very interesting in light of the ancient DNA evidence that has come out in the last couple years:
In addition to the pattern described in the main text, the SARD sample seemed to have played a major role as source of admixture for most of the examined populations, especially Italian ones, rather than as recipient of migratory processes. In fact, the most significant f3 scores for trios including SARD indicated peninsular Italians as plausible results of admixture between SARD and populations from Iran, Caucasus and Russia. This scenario could be interpreted as further evidence that Sardinians retain high proportions of a putative ancestral genomic background that was considerably widespread across Europe at least until the Neolithic and that has been subsequently erased or masked in most of present-day European populations. [25]
Sarno et al. (2017) concentrate on the genetic impact brought by the historical migrations around the Mediterranean on Southern Italy and Sicily, and conclude that the "results demonstrate that the genetic variability of present-day Southern Italian populations is characterized by a shared genetic continuity, extending to large portions of central and eastern Mediterranean shores", while showing that "Southern Italy appear more similar to the Greek-speaking islands of the Mediterranean Sea, reaching as far east as Cyprus, than to samples from continental Greece, suggesting a possible ancestral link which might have survived in a less admixed form in the islands", also precises how "besides a predominant Neolithic-like component, our analyses reveal significant impacts of Post-Neolithic Caucasus- and Levantine-related ancestries." [14] A news article associated with the Max Planck Society, reviewing the results, while beginning by stating that "populations along the eastern Mediterranean coast share a genetic heritage that transcends nationality", also points out how this study is interesting on the debates concerning the diffusion of the Indo-European languages family in Europe, as, while showcasing the influence from the Caucasus, there's no genetic marker associated with the Pontic–Caspian steppe, "a very characteristic genetic signal well represented in North-Central and Eastern Europe, which previous studies associated with the introduction of Indo-European languages to the continent." [14]
Raveane et al. (2019) discovered in a genome-wide study on modern-day Italians a contribution of Caucasus Hunter-Gatherers from the third millennium Anatolian Bronze Age, predominantly in Southern Italy. Furthermore, patterns of regional variation showed geographical structure in Southern Italy, Northern Italy, and Sardinia, in line with previous studies. Even more detailed structure was observed between subregional clusters, caused by geography and distance, and historical admixture possibly associated with events at the end of the Roman Empire and during subsequent periods. [4]
Antonio et al. (2019) studied historical populations from various time periods in Latium and Rome. They found that, despite the linguistic differences, the Latins and the Etruscans showed no significant genetic differences. Their autosomal DNA was a mixture in similar proportions of Western Hunter-Gatherers (Mesolithic), Early European Farmers (Neolithic), and Western Steppe Herders (Bronze Age). [2]
A 2022 genome-wide study of more than 700 individuals from the South Mediterranean area (102 from Southern Italy), combined with ancient DNA from neighbouring areas, found high affinities of South-Eastern Italians with modern Eastern Peloponnesians, and a closer affinity of ancient Greek genomes with those from specific regions of South Italy than modern Greek genomes. The study also discovered common genetic sources shared between South Italy and Peloponnese, which can be modeled as a mixture of Anatolian Neolithic and Iranian Chalcolithic ancestries. [106]
Monnereau et al (2024) analyzed burials at the site of Segesta to investigate the interactions between Muslim and Christian communities during the Middle Ages in Sicily. The biomolecular and Isotopic results suggest the Christians remained genetically distinct from the Muslim community at Segesta while following a substantially similar diet. Based on these results, the authours suggest that the two communities at Segesta could have followed endogamy rules. [107]
Cardium pottery or Cardial ware is a Neolithic decorative style that gets its name from the imprinting of the clay with the heart-shaped shell of the Corculum cardissa, a member of the cockle family Cardiidae. These forms of pottery are in turn used to define the Neolithic culture which produced and spread them, commonly called the "Cardial culture".
Genetics and archaeogenetics of South Asia is the study of the genetics and archaeogenetics of the ethnic groups of South Asia. It aims at uncovering these groups' genetic histories. The geographic position of the Indian subcontinent makes its biodiversity important for the study of the early dispersal of anatomically modern humans across Asia.
Haplogroup R, or R-M207, is a Y-chromosome DNA haplogroup. It is both numerous and widespread among modern populations.
The genetic history of Europe includes information around the formation, ethnogenesis, and other DNA-specific information about populations indigenous, or living in Europe.
The genetic history of the Middle East is the subject of research within the fields of human population genomics, archaeogenetics and Middle Eastern studies. Researchers use Y-DNA, mtDNA, and other autosomal DNA tests to identify the genetic history of ancient and modern populations of Egypt, Persia, Mesopotamia, Anatolia, Arabia, the Levant, and other areas.
The genetic history of the British Isles is the subject of research within the larger field of human population genetics. It has developed in parallel with DNA testing technologies capable of identifying genetic similarities and differences between both modern and ancient populations. The conclusions of population genetics regarding the British Isles in turn draw upon and contribute to the larger field of understanding the history of the human occupation of the area, complementing work in linguistics, archaeology, history and genealogy.
In classical antiquity, several theses were elaborated on the origin of the Etruscans from the 5th century BC, when the Etruscan civilization had been already established for several centuries in its territories, that can be summarized into three main hypotheses. The first is the autochthonous development in situ out of the Villanovan culture, as claimed by the Greek historian Dionysius of Halicarnassus who described the Etruscans autochthonous people who had always lived in Etruria. The second is a migration from the Aegean Sea, as claimed by two Greek historians: Herodotus, who described them as a group of immigrants from Lydia in Anatolia, and Hellanicus of Lesbos who claimed that the Tyrrhenians were the Pelasgians originally from Thessaly, Greece, who entered Italy at the head of the Adriatic Sea in Northern Italy. The third hypothesis was reported by Livy and Pliny the Elder, and puts the Etruscans in the context of the Rhaetian people to the north and other populations living in the Alps.
African admixture in Europe refers to the presence of human genotypes attributable to periods of human population dispersals out of Africa in the genetic history of Europe.
Genetic studies of Jews are part of the population genetics discipline and are used to analyze the ancestry of Jewish populations, complementing research in other fields such as history, linguistics, archaeology, and paleontology. These studies investigate the origins of various Jewish ethnic divisions. In particular, they examine whether there is a common genetic heritage among them. The medical genetics of Jews are studied for population-specific diseases.
Population genetics research has been conducted on the ancestry of the modern Turkish people in Turkey. Such studies are relevant for the demographic history of the population as well as health reasons, such as population specific diseases. Some studies have sought to determine the relative genetic contributions of the Turkic peoples of Central Asia, from where the Seljuk Turks began migrating to Anatolia after the Battle of Manzikert in 1071, which led to the establishment of the Anatolian Seljuk Sultanate in the late 11th century, and prior populations in the area who were culturally assimilated during the Seljuk and the Ottoman periods.
The ancestry of modern Iberians is consistent with the geographical situation of the Iberian Peninsula in the South-west corner of Europe, showing characteristics that are largely typical in Southern and Western Europeans. As is the case for most of the rest of Southern Europe, the principal ancestral origin of modern Iberians are Early European Farmers who arrived during the Neolithic. The large predominance of Y-Chromosome Haplogroup R1b, common throughout Western Europe, is also testimony to a sizeable input from various waves of Western Steppe Herders that originated in the Pontic-Caspian Steppe during the Bronze Age.
The genetic history of North Africa encompasses the genetic history of the people of North Africa. The most important source of gene flow to North Africa from the Neolithic Era onwards was from Western Asia, while the Sahara desert to the south and the Mediterranean Sea to the north were also important barriers to gene flow from sub-Saharan Africa and parts of Europe in prehistory. However, North Africa is connected to Western Asia via the Isthmus of Suez and the Sinai peninsula, while at the Straits of Gibraltar, North Africa and Europe are separated by only 15 km (9 mi), similarly Malta, Sicily, Canary Islands, Lampedusa and Crete are close to the coasts of North Africa, with the indigenous Guanche people of the Canary Islands being Berber.
The genetic history of Egypt reflects its geographical location at the crossroads of several major biocultural areas: North Africa, the Sahara, the Middle East, the Mediterranean and sub-Saharan Africa.
The Bulgarians are part of the Slavic ethnolinguistic group as a result of migrations of Slavic tribes to the region since the 6th century AD and the subsequent linguistic assimilation of other populations.
Population genetics is a scientific discipline which contributes to the examination of the human evolutionary and historical migrations. Particularly useful information is provided by the research of two uniparental markers within our genome, the Y-chromosome (Y-DNA) and mitochondrial DNA (mtDNA), as well as autosomal DNA. The data from Y-DNA and autosomal DNA suggests that the Croats mostly are descendants of the Slavs of the medieval migration period, according to mtDNA have genetic diversity which fits within a broader European maternal genetic landscape, and overall have a uniformity with other South Slavs from the territory of former Yugoslavia.
Early European Farmers (EEF) were a group of the Anatolian Neolithic Farmers (ANF) who brought agriculture to Europe and Northwest Africa. The Anatolian Neolithic Farmers were an ancestral component, first identified in farmers from Anatolia (also known as Asia Minor) in the Neolithic, and outside in Europe and Northwest Africa, they also existed in Iranian Plateau, South Caucasus, Mesopotamia and Levant. Although the spread of agriculture from the Middle East to Europe has long been recognised through archaeology, it is only recent advances in archaeogenetics that have confirmed that this spread was strongly correlated with a migration of these farmers, and was not just a cultural exchange.
In archaeogenetics, western hunter-gatherer is a distinct ancestral component of modern Europeans, representing descent from a population of Mesolithic hunter-gatherers who scattered over western, southern and central Europe, from the British Isles in the west to the Carpathians in the east, following the retreat of the ice sheet of the Last Glacial Maximum. It is closely associated and sometimes considered synonymous with the concept of the Villabruna cluster, named after Ripari Villabruna cave in Italy, known from the terminal Pleistocene of Europe, which is largely ancestral to later WHG populations.
This article summarizes the genetic makeup and population history of East Asian peoples and their connection to genetically related populations such as Southeast Asians and North Asians, as well as Oceanians, and partly, Central Asians, South Asians, and Native Americans. They are collectively referred to as "East Eurasians" in population genomics.
In archaeogenetics, the term Western Steppe Herders (WSH), or Western Steppe Pastoralists, is the name given to a distinct ancestral component first identified in individuals from the Chalcolithic steppe around the turn of the 5th millennium BC, subsequently detected in several genetically similar or directly related ancient populations including the Khvalynsk, Repin, Sredny Stog, and Yamnaya cultures, and found in substantial levels in contemporary European, Central Asian, South Asian and West Asian populations. This ancestry is often referred to as Yamnaya ancestry, Yamnaya-related ancestry, Steppe ancestry or Steppe-related ancestry.
The genetic history of Africa summarizes the genetic makeup and population history of African populations in Africa, composed of the overall genetic history, including the regional genetic histories of North Africa, West Africa, East Africa, Central Africa, and Southern Africa, as well as the recent origin of modern humans in Africa. The Sahara served as a trans-regional passageway and place of dwelling for people in Africa during various humid phases and periods throughout the history of Africa. It also served as a biological barrier that restricted geneflow between the northern and central parts of Africa since its desertification, contributing to the diverse and distinct population structures on the continent. Nonetheless, this did not stop contact between peoples north and south of the Sahara at various points, especially in prehistoric times when the climate conditions were warmer and wetter.
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: CS1 maint: DOI inactive as of December 2024 (link)Interestingly, although Iron Age individuals were sampled from both Etruscan (n=3) and Latin (n=6) contexts, we did not detect any significant differences between the two groups with f4 statistics in the form of f4(RMPR_Etruscan, RMPR_Latin; test population, Onge), suggesting shared origins or extensive genetic exchange between them. ... In the Medieval and early modern periods (n = 28 individuals), we observe an ancestry shift toward central and northern Europe in PCA (Fig. 3E), as well as a further increase in the European cluster (C7) and loss of the Near Eastern and eastern Mediterranean clusters (C4 and C5) in ChromoPainter (Fig. 4C). The Medieval population is roughly centered on modern-day central Italians (Fig. 3F). It can be modeled as a two-way combination of Rome's Late Antique population and a European donor population, with potential sources including many ancient and modern populations in central and northern Europe: Lombards from Hungary, Saxons from England, and Vikings from Sweden, among others (table S26).
The genetic contribution of Greek chromosomes to the Sicilian gene pool is estimated to be about 37% whereas the contribution of North African populations is estimated to be around 6%.
Interestingly, although Iron Age individuals were sampled from both Etruscan (n=3) and Latin (n=6) contexts, we did not detect any significant differences between the two groups with f4 statistics in the form of f4(RMPR_Etruscan, RMPR_Latin; test population, Onge), suggesting shared origins or extensive genetic exchange between them.
As a matter of fact, while the presence of J2a-M67* suggests contacts by sea with Anatolian people, in agreement with the Herodotus hypothesis of an external Anatolian source of Etruscans, the finding of the Central European lineage G2a-L497 at considerable frequency would rather support a Northern European origin of Etruscans. On the other hand, the high incidence of European R1b lineages cannot rule out the scenario of an autochthonous process of formation of the Etruscan civilization from the preceding Villanovan society, as first suggested by Dionysius of Halicarnassus; a detailed analysis of haplogroup R1b-U152 could prove very informative in this regard.
The Grotta La Sassa (National Cave Cadastre id: LA 2001) was discovered in 2015 during a survey of the Ausoni Mountains natural caves carried out by two speleological groups: Gruppo Grotte Castelli Romani and Speleo Club Roma. (...) At La Sassa, the two males LSC002/004 and LSC011 have an identical Ychr haplotype (J2a-M410/J2a7-Z2397; Table 1; Data S1B and S1F)
It's likely that Basque, Paleo-Sardinian, Minoan, and Etruscan developed on the continent in the course of the Neolithic Revolution. Sadly, the true diversity of the languages that once existed in Europe will never be known.
4/138=2.9% in Latium; 3/114=2.6% in Volterra; 2/92=2.2% in Basilicata and 3/154=2.0% in Sicily