history:ev_human
Table of Contents
Evolution of Humans
- see also:
Speculative family tree:
pre-humanoid ancestry:
pre-vertebrate evolution
- eumetazoa (true tissues organized into germ layers, and an embryo that goes through a gastrula stage) ?Ediacaran c600-635mya
- bilateria (animals having a bilateral symmetry) ?585mya
- deuterostomes (two mouths - first opening (the blastopore) becomes the anus) ~558mya eg. the < 1mm Saccorhytus 1)
- chordates (earliest fish Cambrian)
- vertebrate fish
vertebrate evolution
- vertebrate fish - 485-525mya (Cambrian explosion)
- gnathostomata (jawed fish, Ordovician)
- eugnathostomata
- teleostomi
- osteichthyes (bony fish)
- sarcopterygii (lobe-finned fish) some developed spiracles (these evolved into ears) and lungs to breath air and then nostrils (such as the Gogonasus 380mya late Devonian)
- tetrapoda (4 limbed vertebrates with radius, ulna, humerus, femur, tibia, fibula, middle ear, spiracles, nostrils, lungs; 395mya)
- amphibian reptiliomorphs 340mya
- basal amniotes (egg equipped with an amnios)
- later amniotes
- primitive synapsid reptiles (the other group of amniotes evolved into sauropsida which evolved into modern reptiles and birds)
- eupelycosauria (pelycosaurs)
- sphenacodontia (caniniform teeth and thickened maxilla)
- therapsids 275mya (all non-therapsid pelycosaurs, as well as many other life forms, became extinct at the end of Permian period)
- neotherapsida (Permian onwards)
- theriodonts (“mammal-like teeth”) 265mya
- eutheriodontia (Middle Permian) - loss of teeth on the palate
- cynodonts (“dog-teeth”, Late Permian) - 260mya
- probainognathian
- prozostrodontia (Late Triassic)
- mammaliaformes (fixed dentition - primary and secondary teeth)
- mammalia (mammary glands)
- theriiformes (Mesozoic)
- eutheria (placentals) - 160mya
- boreoeutheria (most males have external testes)
- euarchontoglires (supraprimates including rodents)
- cobalamin synthetase gene from bacteria integrated to synthesize B12
- euarchonta (excludes rabbits, rodents)
- primatomorpha
- primates - 80mya
- haplorhines (dry nosed) - 63mya
- anthropoidea - 58mya
- catarrhini (Old World Monkeys) - 40 mya
primate evolution into humans
- primitive insectivore mammals
- it is thought that increased levels of testosterone may have contributed to the increasing brain size seen in primates but then a reduction helped socialization of hominids
- Deleted in AZoospermia (DAZ) gene 1st appears 30-40mya
- pre-monkeys (anthropoids)
- diet extended to fruit, nuts, leaves; eyes more anterior ⇒ 3D vision; manipulating limbs
- originated in Asia 45mya, some migrated to Africa 38mya while a colder global climate 34mya resulted in extinction of most monkey-like anthropoids in Europe, Nth America and Asia (except the Bahinia banyueae in Asia) and instead lemur-like anthropoids dominated in Asia
- New World monkeys - did not evolve to apes
- Old World monkeys of Africa (25-35m yrs ago) - long, balancing tails; increasing body size; brachiating ⇒ arboreal; unlike all other mammals branching prior in the evolution tree, do not produce alpha galactose;
- 25mya: loss of tails is thought to be due to insertion of a DNA snippet called AluY into the TBXT gene's regulatory code in the ancestors of apes and humans 2)
- hominoidea (Apes) - 20.4mya - distinguished from other primates by a wider degree of freedom of motion at the shoulder joint as evolved by the influence of brachiation.
- gibbons (~15-16mya) (Lesser Apes)
- hominidae (Great Apes) (~15-16mya)
- forest-dwelling apes
- orangutans
- hunting apes (~15m yrs ago)
- gorillas 8.8mya (all have blood group type B)
- ? aquatic “naked ape” hunters:
- reduced hair, streamlined hair patterns & more erect posture for swimming
- hair remaining on head to prevent solar damage
- thick subcutaneous layer of fat to prevent heat loss
- improved hand capabilities to feel for food underwater
- homo-chimp ~ 6-8mya (split from gorillas and evolved cooperative aggression to maintain territories)
- chimpanzee 6.3mya (all have blood group type A)
- hominids - 6.3mya (split from chimpanzees)
- chimpanzee chromosomes 2A and 2B fused to form hominid chromosome 2
- over 80 chimpanzee genes were lost in human evolution including 36 for olfactory receptors, a type I hair keratin gene (perhaps lost 240,000yrs ago), sarcomeric myosin gene MYH16 (5.3mya perhaps resulted in smaller masticatory muscles) and CASPASE12, a cysteinyl aspartate proteinase which may have resulted in improved resistance to bacterial infection in humans
- natural selection resulted in Human accelerated regions in the genome such as HAR1F, which is believed to be related to brain development and HAR2 (a.k.a. HACNS1) which may be related to the opposable thumb.
- DAZ “doubled” about the same time that “Y Chromosome Adam” appears in human evolution
- Graecopithecus freybergi ~7.2mya fossils found in Greece, Bulgaria
- Sahelanthropus tchadensis ~7mya, fossils found in Chad
- chimp-sized human ancestor, Orrorin tugenensis, that walked upright 6m yrs ago in Kenya (disc. 2004)
- oldest found human ancestor “Toumai” (6-7m yrs ago) disc. in Chad in 2001
- Ardipithecus 5.6mya
- australopiths ~4-5mya
- enzyme which makes Neu5Gc, CAMH, is mutated 2.1-2.2mya hence huans do not make a common mammalian sialic acid (Neu5Gc), this may also have contributed to the increasing hominid brain
- Homo ~1.8mya
- Homo sapiens (modern human) 250,000-350,000 yrs ago (oldest fossil - Morocco 2017)
Common human ancestor (Africa 5m yrs ago)
- Ardipithecus ramidus (Ethiopia 4.4m yrs ago)
- Australopithecus anamensis (Kenya 4.2m yrs ago)
- use of stone tools commenced c 3.3mya in Kenya
- A. bahrelghazali (Chad 3-3.5m yrs ago)
- A. afarensis (Ethiopia, Tanzania 3.5 m yrs ago)
- c3mya, long before H. erectus, hominids lose Neu5Gc sialic acid gene and instead produce more Neu5Ac sialic acid
- this seems to play a role in susceptibility to diseases thought to be unique to humans, such as typhoid and cholera, as well as sexually transmitted diseases such as chlamydia, syphilis and gonorrhoea with the pathogens coating themselves in the hominid kind of sialic acid to escape the immune system
- Plasmodium falciparum however perhaps only became a problem for humans 10,000yrs ago when it mutated to target Neu5Ac when humans adopted agrarian lifestyles near stagnant pools of water
- Beef, pork and lamb contain large amounts of Neu5Gc, and when humans consume this non-human sugar molecule it gets incorporated into our cells and may result in chronic inflammation and cancer and may be linked to infertility
- humans also possess a modified version of a sugar-binding gene receptor known as CD33, which is found on immune cells – and the mutated version we possess is missing this sugar-binding site (also missing in chimps, Neanderthals and Denisovans), no longer reacts to sialic acids on damaged cells and plaques, allowing the microglia to break them down and having higher levels of this CD33 variant is protective against Alzheimer’s and may better allow the grandmother care of children and also reduce gonorrhoea which coat themselves in the sugar that CD33 usually binds to
- Paranthropus aethiopicus (Eastern Africa 2.7m yrs ago)
- P. robustus (Sth Africa 2.5m yrs ago)
- P. boisei (Eastern Africa 1.4-2.5m yrs ago)
- A. garhi (Ethiopia 2.6m yrs ago)
- A. africanus (Sth Africa 2-3m yrs ago) - 1st australopith to be discovered (in 1924); use of stone tools; oldest stone tools found outside of Africa, are 1.3-2.1m yrs old in Shangchen region of China perhaps made by an ancestor of H. erectus, while those found in Dmanisi, Georgia are dated to 1.85mya
- H. rudolfensis (Eastern Africa 2m yrs ago)
- hominids lose body hair and allows heat loss through perspiration to allow a more active lifestyle in hot environments and thus melatonin content of skin increases to protect from UV radiation and also reduces UV-A mediated breakdown of folate which is important for sperm and fetal neural tube development (c1.5-2mya)
- it seems a selective sweep occurred c1.2 mya ago that favored MC1R variants producing eumelanin‐rich protective pigmentation on effectively naked skin primarily to protect against UV radiation (but also has some added protection against tropical infections and may be protective against degradation of folate) - levels of UV-B radiation is the most important determinant of levels of eumelanin in skin 3)
- multiple derived alleles contributed to the evolution of dark pigmentation in ancestral H. sapiens. These include two derived alleles of the major facilitator superfamily domain‐containing protein 12 (MFSD12), which appeared at or near the time of origin of H. sapiens, about 0.3 mya
- there was further skin darkening in regions of the world including East Africa, parts of South Asia, and Melanesia with extremely high environmental UVR
- those hominids who migrated into lower UV-B latitudes such as Eurasia ran into vitamin D deficiency issues with immune impairment and critically, ricket affected pelvis which would not allow births and thus melatonin content evolved to be reduced - not even Australia has enough UV-B to provide sufficient Vit D for the darkest skinned hominids without resorting to supplementary Vit D intake such as oily fish (eg. Inuits who evolved a heightened ability to tan to cope with high levels of reflected UV-A from snow and ice) or lichen-eating reindeer (eg. Finnish) - this effect occurred again with H. erectus and with H. neandertherthalensis and twice later with Homo sapiens migrating. When hominids re-invaded high UV zones, they evolved darker pigmentation again (eg. northern India H. sapiens moving to southern India 20,000yrs ago). Those who evolved in mid-latitudes of UV such as the Mediterranean (less than 40degN) gained the ability to tan.
- 900,000yrs ago: 98.7% of hominids were wiped out leaving only 1280 breeding individuals to sustain a population for ~117,000 yrs according to genomic sequencing
- this event was consistent with the fusion of two progenitor chromosomes, presently identified as chromosome 2 in extant human populations.
- coincided with climate changes that turned glaciation into long-term events, a decrease in marine surface temperatures, and a possible long period of drought in Africa and Eurasia
- helps explain the loss of African and Eurasian fossil evidence in the Early Stone Age
- oldest preserved example of a wooden structure being worked is c476,000yrs ago in Zambia (https://www.youtube.com/watch?v=umB8dzt7jgM))
- H. habilis (Sub-saharan Africa 1.8m yrs ago) - 1st found in 1960 in Tanzania
- H. ergaster (Eastern Africa 1.7m yrs ago) - 1st hominid of essentially modern form; hominids reach Java/China by 1.8m yrs ago; hand axe;
- H. erectus (Sth Africa, Eastern Asia 2m-40,000 yrs ago)
- 2mya fossil found in Drimolen cave system north of Johannesburg published in 20204)
- likely used land bridges to reach Indonesia around 1 million years ago
- use of hafted stone-tipped spears for hunting commenced c500,000yrs ago
- H. floresiensis (Flores, Indonesia until 13,000 yrs ago ?until 16thC AD, disc. 2004) - small brain, 1m tall
- the island of Flores is also home to extant pygmies who appear to have Denisovan and Neanderthal DNA but no other archaic DNA evident suggesting their restricted height is a selection cause 5)
- H. luzonensis (Phillipines, 50-67,000ya)
- 3-4' tall with premolars having two or three roots, similar to H. erectus, and very small molars with only single roots, and has curved finger and toe bones which resemble those of Australopithecus
- H. naledi (Sth Africa, ~300,000yrs ago; small brain, mixed primitive and modern features)
- H. antecessor (Spain ?1m-0.7m yrs ago)
- H. heidelbergensis (throughout Old World ?1m-0.6m yrs ago)
- H. denisova (?1mya to 30,000yrs ago) - arose from Africa and spread to Siberia to Papua New Guinea
- Denisovans interbred with Neanderthals and H Sapiens and contributed significantly to the gene pool of H. sapiens in SE Asia and Melanesia
- H. neandertherthalensis (arose from Africa and spread to Europe & Western Asia ?600,000-40,000 yrs ago)
- it appears inter-breeding with H. sapiens resulted in their defective Y chromosome being selectively replaced by H. sapiens' Y chromosome more than 100,000 yrs ago and it seems the common ancestor for both Y chromosomes i estimated to have been around 370,000 yrs ago.6)
- population peaked ~120,000yrs ago at an estimated 70,000 and were generally in small groups of ~20 and had high levels of in-breeding
- had a partial Rh variant, RhD DIII type 4, ~100,000yrs ago which has only been found otherwise in African hominids and had been unknown in modern humans until found in one Australian indigenous person in 2019 and in a few Papuans, thus it is likely that they passed this gene to some H.sapiens prior to 65,000yrs ago 7)
- H. sapiens
- 250,000-350,000 yrs ago in Africa; 40,000 yrs ago in Europe; to present
- earliest fossil record is 315,000 yr old fossil from Morocco, and a 210,000 yr old fossil from Greece (but this group appears not to have survived in this early wave of migration from Africa)
- use of bows and arrows for hunting commenced around 70,000yrs ago
- creativity; art; symbolic thought;language;
- c70,000yrs ago, those migrating to:
- southern Asia, Australia and Melanesia evolved increased darkening of skin
- eastern Asia evolved lighter skin due to relaxation of selection for MC1R and positive selection of KITLG variant
- and later, particularly when agriculture commenced and vitamin D intakes fell, those in near east evolved lighter skin by positive selection for SLC24A5 variant which would then migrate to north-western Europe
the migration and diversification of Homo sapiens
- oldest known H.sapiens c300,000BC in Morocco (disc. 2017), although anatomically modern humans appear to have evolved in northern Botswana 160,000-240,000 yrs ago making the Moroccan dating incongruous.
- 120,000 yrs ago began cooking tubers and rhizomes to increase dietary starch in Sth Africa which presumably led to a duplication of the starch digestion genes
- oldest known rock painting c71,000BC in Sth Africa
- the Ice Age ( (100,000BC - 12,000BC) lowered sea levels and allowed easier migration in some areas such as the drying up of the North Sea (although the extensive glaciation would have made survival tough away from the tropics)
- DNA analysis suggests humans migrated out of Africa 50,000-60,000 yrs ago in one migration:
- initially via the coast of India to Australia and New Guinea taking 5,000-6,000yrs, creating the Aboriginal population in Australia such as in Lake Mungo in 40,000-50,000 yrs ago - one of the first H. sapiens colonies outside of Africa.
- the Polynesians migrated much later, starting around 3000BC and migrated from Taiwan region to eventually cover most of the Pacific Islands, and eventually to Hawaii
- migrated to Europe reaching the Atlantic within 2,500yrs from the Balkans as follows, and presumably resulted in the demise of the indigenous Neanderthal population over some 6000 yrs (Nature Feb 2006):
- Middle East by 46,000BC
- Istanbul by 44,000BC
- Italy, and central Europe by 40,000BC
- Spain, France, and eastern Europe by 39,000BC
- world's earliest cave paintings (SE France) dated at 29,000-34,000BC
- reached Madagascar ~8000BC
- 18 daughters of Eve:
- almost all American Indians have mtDNA that belong to lineages he named A, B, C and D
- Europeans belong to lineages H through K and T through X
- Asia the ancestral lineage is known as M, with descendant branches E, F and G
- In Africa there is a single main lineage, known as L, which is divided into three branches. L3, the youngest branch, is common in East Africa and is believed to be the source of both the Asian and European lineages.
- the oldest of this maternal mitochondrial lineage, L0, of anatomically modern humans, is believed to have originated in northern Botswana 165,000 to 240,000yrs ago8), from here they dispersed north-eastwards and south-westwards around 110,000-130,000 yrs ago when increased humidity led to green corridors being opened. Further migration to east Africa occurred 60,000-70,000yrs ago
- 7 European daughters of Eve based on mitochondrial DNA studies - all descended from the Lara clan - one of 3 clans still existing in Africa:
- Helena: This clan lived in the ice-capped Pyrenees. As the climate warmed, Helena’s descendants trekked northward to what is now England, some 12,000 years ago. Members of this group are now present in all European countries.
- Jasmine: Her people had a relatively happy life in Syria, where they farmed wheat and raised domestic animals. Jasmine’s descendants traveled throughout Europe, spreading their agricultural innovations with them.
- Katrine: Members of this group lived in Venice 10,000 years ago. Today most of Katrine’s clan lives in the Alps.
- Tara: Sykes’ maternal ancestry goes back to this group, which settled in Tuscany 17,000 years ago. Descendants ventured across northern Europe and eventually crossed the English Channel.
- Ursula: Users of stone tools, Ursula’s clan members drifted across all of Europe.
- Valda: Originally from Spain, Valda and her immediate descendants lived 17,000 years ago. Later relatives moved into northern Finland and Norway.
- Xenia: Her people lived in the Caucasus Mountains 25,000 years ago. Just before the Ice Age, this clan spread across Europe, and even reached the Americas. [As Dr. Wallace discovered, the X pattern is a rare European lineage and is also among the northern Native Americans such as the Ojibwa and Sioux.]
- 10 sons of a genetic Adam based on Y chromosomal analysis:
- I, II, III are found almost exclusively in Africa
- III's sons' lineage migrated to Asia and fathered sons IV-X
- IV - Sea of Japan
- V - northern India
- VI and IX - South Caspian
- 10 founding fathers of Europeans:
- three waves of migrations to Europe: 40,000, 22,000, and 9,000 years ago.
- 95% of European men can trace themselves to 1 of 10 male ancestors
- More than 80 percent of European men inherited y-DNA from Paleolithic ancestors who lived in Europe 25,000 to 40,000 years ago
- The other twenty percent inherited from Neolithic farmers in Europe 9,000 to 10,000 years ago
- gene for thallaesemia identified in a hunter-gatherer Vietnamese man 7000yrs ago suggesting malaria was an issue in SE Asia before farming practices commenced9)
European hunter-gatherers
- modern humans left sub-Saharan Africa at least 60 thousand years ago (ka), and during their initial expansion into Eurasia, they genetically mixed with Neanderthals, resulting in 2–3% Neanderthal ancestry in the majority of present-day non-African population
- Ancient East Eurasians c43,000BC
- Australasian lineage
- Ancient Ancestral South Indian lineage
- East and Southeast Asian lineage
- modern humans have populated Europe for more than 45,000 years
- Genomic data have shown that modern humans were present in western Eurasia at least 45 ka and mixed with Neanderthals
- Surprisingly, however, none of those pre-40 ka individuals left substantial traces in the genetic makeup of present-day Eurasian populations and appear to have become extinct
- The oldest genomes carrying ancestries that derive primarily from the lineage leading to present-day Europeans are:
- Kostenki 14 (from 37 ka, with uncertain archaeological association from western Russia)
- contributed to the later Věstonice genetic cluster (hereafter, Věstonice cluster or ancestry), named after the Dolní Věstonice site in Czechia
- 'Early West Eurasian' hunter-gatherers'
- these merged with an 'Early East Eurasian' population to form the Ancient North Eurasian (ANE) c22000BC Mal'ta–Buret' culture in Siberia and who would go on to essentially populate most of Europe in the Neolithic period
- this genetic signature is shared among individuals associated with the archaeologically defined Gravettian culture (33–26 ka) in central and southern Europe and seemingly disappeared after the Last Glacial Maximum (LGM)
- possibly some of the Siberians migrated to America during this period
- Goyet Q116-1 (35 ka, Aurignacian-associated from Belgium)
- After the LGM, a genetic component distantly linked to the Goyet Q116-1 individual from Belgium dated to 35 ka—named GoyetQ2 ancestry (hereafter, GoyetQ2 cluster or ancestry)—reappeared in individuals from southwestern and central Europe associated with the Magdalenian culture (19–14 ka from Iberia to eastern Europe across central Europe) and in an admixed form in subsequent Final Palaeolithic and Mesolithic hunter-gatherers, but the geographic extension of this ancestry is still unclear
- Bacho Kiro 1653 (35 ka, probably Aurignacian-associated from Bulgaria)
- Gravettians
- individuals associated with the Gravettian culture across Europe were not a biologically homogeneous population, culturally, however, we see both widespread general tendencies, such as weaponry and some portable art, and other aspects that have a more regional character, such as mortuary practices, various originalities in lithic and hard organic materials tool kits and adornments
- The ancestry found in individuals associated with the Aurignacian culture from central Europe (GoyetQ116-1 ancestry) gave rise to Gravettian-associated individuals from western and southwestern Europe. This derived ancestry—the Fournol cluster—survived during the LGM in Solutrean-associated individuals, possibly within the Franco-Cantabrian climatic refugium, leading to later populations associated with the Magdalenian culture (GoyetQ2 cluster and El Mirón)
- the ancestry found in pre-30 ka eastern European individuals (Kostenki cluster and Sunghir group) contributed to Gravettian-associated individuals from central and southern Europe (Věstonice cluster), the latter without descendants retrieved in post-LGM populations from those regions
- a genetic ancestry profile in individuals associated with Upper Palaeolithic Gravettian assemblages from western Europe that is distinct from contemporaneous groups related to this archaeological culture in central and southern Europe, but resembles that of preceding individuals associated with the Aurignacian culture.
- Last Glacial Maximum LGM (25,000 to 19,000 years ago)
- is considered to have caused a demographic decline in large parts of Europe with populations retracting to southern latitudes as attested—for example—by the contemporaneity of the Solutrean culture (24–19 ka) in the Iberian peninsula and southern France.
- Other proposed climatic refugia for human survival during this period are the Italian peninsula, the Balkans and the southeastern European Plain, but the actual genetic contribution of populations from these regions to post-LGM Europeans is highly debated
- Epigravettians
- a genetic turnover in southern Europe suggesting a local replacement of human groups around the time of the Last Glacial Maximum, accompanied by a north-to-south dispersal of populations associated with the Epigravettian culture.
- the ancestry of individuals associated with the Epigravettian culture (Villabruna cluster), which was found to genetically connect European and Near Eastern hunter-gatherers, reached southern Europe well before the transition between the Early and Late Epigravettian and possibly as early as the Gravettian–Epigravettian transition.
- A phylogeographic reconstruction of different lineages carrying this ancestry further suggests its entry point into northeastern Italy from the Balkans followed by a north-to-south expansion into the Italian peninsula alongside a population decline through sequential bottlenecks.
- in southern Europe, a distinct hunter-gatherer genetic profile was found as early as 17 ka in individuals associated with the Epigravettian culture (24–12 ka, from the Italian peninsula to the southeastern European Plain across the Balkans). This ‘Villabruna’ ancestry (hereafter, Villabruna cluster or ancestry) showed connections to ancient and present-day Near Eastern populations, but the mode and tempo of its expansion into the Italian peninsula remain unexplored. The Villabruna ancestry later appeared in central Europe and it is thought to have largely replaced groups related to the GoyetQ2 ancestry
- Magdalenians
- Magdalenian-associated individuals not only from Iberia but also from the rest of Europe carry Epigravettian-associated ancestry (Villabruna cluster).
- Genetic analyses of western European individuals associated with the preceding Badegoulian culture might provide clues on the processes that led to the formation of the GoyetQ2 cluster. As inferred from the archaeological record, the spread of the Magdalenian across Europe is linked to southwestern to northern and northeastern post-LGM population expansions and not to movements from southeastern refugia
- large-scale genetic turnover as early as 14 ka in central and western European hunter-gatherers
- From at least 14,000 years ago, an ancestry related to the Epigravettians culture spread from the south across the rest of Europe, largely replacing the Magdalenian-associated gene pool.
- This turnover is associated with multiple techno-complexes—Federmesser, Azilian and other Final Palaeolithic groups —despite considerable technological continuity with the preceding late Magdalenian
- This broadly distributed ancestry (the Oberkassel cluster (also known as WHG)) is most closely related to an Epigravettian-associated individual from northwestern Italy, suggesting that its expansion into continental Europe might have started from the west—and not the east—side of the Alps. Moreover, the almost complete genetic replacement of the Magdalenian-associated gene pool raises the hypothesis that parts of Europe were differentially populated during the abrupt climatic variation starting around 14.7 ka with the Bølling–Allerød warming period, creating areas where southern European populations could expand. This might also explain the genetic uniformity of the Oberkassel cluster across large parts of western Eurasia but genomic data from between 15 and 14 ka is needed to understand the exact dynamics of this turnover.
- Oberkassel and Sidelkino ancestries
- the Oberkassel ancestry in western and central Europe and the Sidelkino ancestry in eastern Europe remained largely isolated for almost 6,000 years until genetic interactions were first observed—around 8 ka in northeastern Germany, possibly associated with cultural exchanges along the Baltics and around 7.5 ka in the upper Volga region, possibly linked to the spread of pottery in the region
- Migration of east Asians from NE China to America
- as determined by mitochondrial DNA evidence, the 1st wave of this was during the LGM 26,000-19.500yrs ago
- it seems likely the 1st Americans arrived during this period via a relatively flat ice bridge formed from ample expanses of winter sea ice which would have enabled migration c24500yrs ago to 14800 yrs ago.
- prior to this, while sea levels were likely to have been low enough to expose a solid bridge across the top of the world as far back as nearly 36,000 years ago, the rugged cap of snow and glacier covering the landscape would have been a struggle, if traversable at all.
- a 2nd wave occurred 19,000-11000yrs ago which also went from China to Hokkiaido, Japan
- Clovis migration theory is based on retreating ice linking Siberia with Alaska around 13,000 years ago
- After a period of limited admixture that spanned the beginning of the Mesolithic, genetic interactions between western and eastern European hunter-gatherers have been found, who were also characterized by marked differences in phenotypically relevant variants.10)
- Emiran culture in the Levant between the Middle Paleolithic and the Upper Paleolithic periods
- remains an enigma as it transitionally has no clear African progenitor
- is among the first periods of the Upper Paleolithic, corresponding to the first stages of the expansion of Homo sapiens out of Africa.
- evolved into the Ahmarian and later the Levantine Aurignacian culture
- European Bohunician culture
- probably linked to the Emiran and Ahmarian, may slightly predate the Ahmarian at 46,000 BC
- Ahmarian culture in the Levant
- 44000-42000BC
- from this stage, the first modern humans migrated to Europe to form the beginning of the European Upper Paleolithic, including the Aurignacian culture, where they become known as the Cro-Magnons
- Aurignacian
- 41000BC-24000BC
- a wave of Homo Sapiens thought to have spread from Africa through the Near East into Paleolithic Europe, and became known as European early modern humans (EEMH), or Cro-Magnons
- migrated throughout much of Europe and created the first European culture of modern humans, the Aurignacian
- this wave includes fossils of the Ahmarian, Bohunician, Aurignacian, Gravettian, Solutrean and Magdalenian cultures
- still part of a large Western Eurasian “meta-population”, related to Central and Western Asian populations
- Levantine Aurignacian in the near eastern Levant
- 33000BC-27000BC
- Kebaran culture in Eastern Mediterranean area
- c21000BC - 12000BC
- highly mobile nomadic population, composed of hunters and gatherers in the Levant and Sinai areas who used microlithic tools
- Tell Qaramel, Syria
- 25 km north of Aleppo, adjacent to the river Quweiq that flows to Aleppo
- possibly inhabited since 16,000BC
- tower built c11000-9670BC perhaps 2000yrs earlier than the Tower of Jericho
- “head cult”: most bodies had their head removed - a similar practice in Jericho, Tell Aswad, and Cayonu
- Natufian culture in the Levant when it was a woodland
- c13000BC-9500BC;
- discovered on the West Bank of the Jordan River
- unusual in that it supported a sedentary or semi-sedentary population even before the introduction of agriculture, although it seems they used wild rye to make a bread-like foodstuff and may have deliberately cultivated rye and possibly brewed beer; pita-like bread 12,500BC;
- Early Natufian (12,000–10,800 BC)
- Late Natufian (10,800–9,500 BC) - most likely occurred in tandem with the Younger Dryas (10,800 to 9,500 BC).
- created one of the 1st permanent settlements in the world: Jericho in 10,000-9000BC
- it was a popular camping ground for Natufian hunter-gatherer groups due to the nearby Ein as-Sultan spring;
- c9600 BCE the droughts and cold of the Younger Dryas stadial came to an end, making it possible for Natufian groups to extend the duration of their stay, eventually leading to year-round habitation and permanent settlement
- epipaleolithic construction at the site appears to predate the invention of agriculture, with the construction of Natufian structures beginning earlier than 9000 BCE
- later (Neolithic to Bronze Age) Levantines primarily genetically derived from Natufians, plus a substantial admixture from Chalcholithic Anatolians.
Neolithic and Chalcolithic (Copper Age) periods
- 8,000–4,500 BC (2,200 BC in Western Europe)
- “Neolithic started in around 10,200 BC in the Levant, arising from the Natufian culture, when pioneering use of wild cereals evolved into early farming.”
- “It lasted in the Near East until the transitional period of the Chalcolithic (Copper Age) from about 4500 BC, marked by the development of metallurgy”
- Pre-Pottery Neolithic / Early Neolithic 10000BC– 6500BC
- as the world warmed up, a new culture based on agriculture and sedentary dwelling emerged in the Levantine and upper Mesopotamian region of the Fertile Crescent
- ended with the 8.2kyr event when there was a 200-400yr period of sudden cooling starting from 6200BC and is part of a 1500yr climate cycle but the cooling was less than during the Younger Dryas.
- domestication of plants and animals was in its formative stages, having possibly been induced by the Younger Dryas.
- further development of Jericho - one of the 1st major proto-cities
- population 200-3000; round mud-brick houses; burial of the dead under the floor of buildings, reliance on hunting wild game, the cultivation of wild or domestic cereals (emmer wheat, barley);
- town was surrounded by a massive stone wall over 3.6 metres (12 ft) high and 1.8 metres (6 ft) wide at the base, inside of which stood a stone tower (the Tower of Jericho), placed in the centre of the west side of the tell. The tower was the tallest structure in the world until the Pyramid of Djoser, and the second-oldest tower after the one at Tell Qaramel in Syria.
- Tell Qaramel, Syria
- possibly inhabited since 16,000BC
- Göbekli Tepe in the Southeastern Anatolia Region of Turkey
- settlement was inhabited from c. 9500 to at least 8000 BCE
- large circular structures that contain massive stone pillars – the world's oldest known megaliths
- Pottery Neolithic / Late Neolithic c7000BC-4500BC
- Proto-Indo-European hunter gatherers
- see section below
- c5000BC, occupied the eastern European (Ukraine/Russian) steppe grasslands having domesticated horses
- these peoples would eventually spread their cultures and languages to most of Europe, Middle East, northern Asia where each of today's languages evolved
- Neolithic Sumerian/Mesopotamia
- Halaf period c6100-5100BC
- continuous development out of the earlier Pottery Neolithic and located primarily in the fertile valley of the Khabur River (Nahr al-Khabur), of south-eastern Turkey, Syria, and Mosul, northern Iraq
- Sumerian civilisation arose c5500-3300BC from a non-semitic black headed West Asian or Nth African people who spoke the Sumerian language
- Ubaid period c5500-3700BC
- Chalcolithic copper smelting period
- occurs at different periods in different areas, and is absent in some parts of the world, such as Russia
- Belovode, on Rudnik mountain in Serbia, has the world's oldest securely dated evidence of copper smelting at high temperature dated to 5000BC
- 4500BC-3200BC in the Levant/Mesopatamia region
- early tin bronze developed independently in Europe 1,500 years before the first tin bronze alloys in the Near East.
- Sumerian/Mesopotamia
- Urek period c4000-3100BC - protoliterate period - Chalcolithic to Early Bronze Age period
- goddess Inanna (goddess of love, war, fertility, and associated with beauty, sex, divine law, and political power) see below
- worshiped in Sumer at least as early as the Uruk period (c. 4000 BCE – 3100 BCE), and her cultic activity was relatively localized before the conquest of Sargon of Akkad. During the post-Sargonic era, she became one of the most widely venerated deities in the Sumerian pantheon.
- c3800BC: city of UR established
- late in this period saw gradual emergence of the cuneiform script which corresponds to the Early Bronze Age
- Jemdet Nasr period c3100 to 2900 BC
- limited to south-central Iraq
- 5th millenium BC: 1st settlements around Hattusa (later became a fortified city and the Hittite capital)
- 1st settlements at Jerusalem c4000BC but 1st written record of Jerusalem is 2000BC as noted by the Egyptians when it was settled by Canaanites albeit with probable Egyptian rule until 1000BC
- rising dominance and spread of the Indo-European hunter gatherers throughout Europe and Nth Asia
- see section below
- Corded Ware culture initially in the forests of Eastern Europe 3000-2400BC
- Bell Beaker Corded Ware Interaction Zone (central Europe)
- Britain, the Chalcolithic is a short period between about 2,500 and 2,200 BC, characterized by the first appearance of objects of copper and gold, a new ceramic culture and the immigration of Beaker culture people derived from the Indo-European hunter gatherers, heralding the end of the local late Neolithic
Bronze age
- 3300-1200BC
- copper or bronze was being used as the chief hard substance for the manufacture of tools and weapons
- c3600BC onwards: expansion of Bantu‐language speakers from western Africa into central, eastern, and southern Africa resulting the continuing evolution of skin pigmentation by population admixture
- c3000BC: Eurasians with lighter skin carrying variants of SLC24A5 giving de-pigmentation spread via the Afro‐Arabian Peninsula into eastern and southern Africa
- Sumerian dynasties / Mesopotamia
- 1st dynasty of UR: c2600-2400 BC
- Sumer was conquered by the Semitic-speaking kings of the Akkadian Empire around 2270 BC
- 3rd dynasty of UR (Neo-Sumerian): 2112-2004BC
- Cycladic culture
- immigration to Cycladic islands in Greece occurred c5000BC and early Cycladic culture began 3300-2000BC
- Helladic Greek
- 3200-1050BC
- Mycenaean civilization 1750 to 1050 BC
- first advanced and distinctively Greek civilization in mainland Greece with its palatial states, urban organization, works of art, and writing system
- dominated by a warrior elite society
- Santorini volcano erupted between 1660 and 1613 BC
- initially mainly mainland people, they also spread across the eastern Mediterranean, interacting with the Minoans of Crete and genetically appear to have contributed to the Peleset group known as "The Sea People" of 1200-900BC some of whom settled in the Levant to form the uncircumcised Philistine population and culture, and also settled in other areas such as Italy.
- after the collapse of the Bronze Age in eastern Mediterranean, Greece fell into the “Greek Dark Ages”, a recordless transitional period leading to Archaic Greece
- Minoan civilisation of Crete
- 2700-1100BC
- Egypt
- 4th millennium BC: Sun God, Ka.; strong belief in the afterlife and mummification process evolved including transnasal excerebration
- 3150BC: 1st recorded unified kingdom under King Menes by the victory of Upper Egypt kingdom over Lower Egypt kingdom
- 2700-2200BC: Old Kingdom
- 2667-2648BC: Pyramid of Djoser; 2589-2566BC: Great Pyramid of Giza;
- 2000-1788BC: earliest evidence of skull trepanation using local anaesthetic of ground marble and vinegar used as a last resort
- 1500BC: Edwin Smith papyrus (describes a series of cases in the format of clinical examination, diagnosis, treatment, and prognosis including head and spine trauma) and the Ebers papyrus (describes different medical treatments for ailments such as migraines), two of the oldest medical records
- Hurrians
- Hurrian kingdom emerged around the city of Urkesh (modern Tell Mozan, Syria) during the third millennium BC
- Indus Valley civilisation
- 2600-1900BC (present day Pakistan)
- Assyrian
- 2025-609BC originated on the Tigris River eg. Niniveh, Assur
- Hittites
- pre 2000BC: fortified capital city of Hattusa - 1st settled 6th millenium BC
- Indo-Europeans or Caucasus peoples in Anatolia c1750-1190BC
- population of the Hittite Empire in Anatolia included a large population of Hurrians and there was significant Hurrian influence in Hittite mythology
- Israelites
- developed from a peasant subset of Canaanites
- Peru
- 3500-1800BC: Norte Chico or Caral-Supe Civilization
- 3rd millenium BC: Sun God, Inti; pyramidal buildings, the importance of the afterlife, tombs for royalty, but unlike Egypt, mummies were not embalmed, and organs left alone; quadrilateral trepanation with burr holes;
- 2627BC: Great Pyramid of Caral
- see Ancient history for more details
Iron age
- see Ancient history
Proto-Indo-Europeans and the spread of their derived languages
Ponto-Caspian Steppe origin theory
- horse riding hunter gatherers become pastoralists (Western Steppe Herders or WSH) in the Ponto-Caspian region 4500-2600BC
- descended from a 5th millenium BC merger between two highly divergent ancestral components (pre-dating resultant Yamnaya culture by 1000yrs):
- Eastern Hunter-Gatherers (EHGs)
- light-intermediate skin color, variable eye color, some with blond hair
- these were mainly derived from:
- Ancient North Eurasian (ANE) ancestry c33000BC and who had blue eyes and fair skin, which was introduced from Siberia via Western Siberian Hunter Gatherers,
- a secondary and smaller admixture of European Western Hunter-Gatherers (WHG)
- Caucasus Hunter-Gatherers (CHGs) c11000BC
- light-intermediate skin color, brown eyes
- 40000BC - origin of blue eyes
- 26000BC-20000BC - origin of light skin
- these peoples were the 1st to domesticate horses in the Volga region of Russia
- their culture was to marry outside of their tribe, and having a high horse protein diet, and the highest ever genetic selection for stature, they were generally bigger and stronger than others in the region which probably explains how they replaced the European neolithic farmers of Central Europe
- expansion of WSHs resulted in the virtual disappearance of the Y-DNA of Early European Farmers (EEFs) from the European gene pool, significantly altering the cultural and genetic landscape of Europe.
- these groups had to manage their size to ensure they did not run out of resources and thus had 3 options:
- expand into new areas
- aggressively attack neighbouring tribes or poach on their land
- expel subsets of the group to live as wolves, especially the younger males who are the most expendable in any society (or kill them) to keep their size down (the optimum maximum size of social human groups is thought to be 150)
- invention of the wheel and thus wagons c3500BC allowed range of these grass steppe dwellers to increase
- ⇒ Yamanaya culture - family groups living in wagons on the steppe (this lasted at least until 450BC)
- 35% of their genes are actually from Caucasus hunter gatherers who spread northwards and admixed with Eastern European hunter gatherers
- ⇒ domestication of the cow
- ⇒ horseback riding 3000BC
- ⇒ megalithic stone circles eg. in Russia
- ⇒ invention of the spoked wheel c2000BC in India?
- spread to:
- Anatolia 4200BC
- ⇒ Armenian 2500BC?
- ⇒ Luwian 2000BC
- ⇒ Hittite 1600BC ?
- Afanaslavo (eastern Russia) 3500-2500BC
- Danube Valley 3300BC
- ⇒ Proto-Greek 2500BC
- ⇒ Thraco-Illyrian 500BC?
- Corded Ware culture 3000-2400BC (forests of east Europe, cleared woods with fire to create pastoralist farms including sheep for wool and farming of cereals with plowing of fields, fired pottery, fermented milk to create cheese, collected honey and made a fermented beverage from it, grinding stones for grains and nuts, trained horses and created some horse riding gear but not a saddle, 2 and 4 wheeled carts with yokes to be pulled by cattle, made copper and gold artefacts, houses with doors, fences, boats, tribes with a wise, powerful, warrior as tribal leader, with agreements and links to other tribes, social classes, elders serve as priests who relate to their gods, others as poets who memorised and recited tribal history, strict rules of hospitality to guests and strangers, yet glorified raiding, the abduction of women and cattle from rival tribes and the total destruction of enemies)
- ⇒ Bell Beaker Corded Ware Interaction Zone (central Europe)
- ⇒ Proto-Germanic 3300BC
- ⇒ Nordic Bronze Age 1700-500BC
- ⇒ Proto-Italic-Celtic (northern Italy) 3000BC
- ⇒ Italic (southern Italy) 1000BC
- ⇒ Bell Beakers (France) 2800-1800BC
- ⇒ Iberian Celts 900BC
- ⇒ British Beaker (England) 2500BC
- ⇒ Fatyanovo-Abashevo (Pre-Proto-Indo-Iranian?) 2900-1900BC
- ⇒ Sintashta-Petrovka (Proto-Indo-Iranian) 2100-1800BC
- ⇒ Andronovo (Indo-Iranian) 2100-1800BC
- ⇒ Tocharian (Mongolia?) 2000BC?
- ⇒
- ⇒ Karasak (?Siberia) 1500BC
- ⇒ Yaz 1500BC ⇒ Iranian
- ⇒ Parthian 800BC
- ⇒ Median 800BC
- ⇒ Bactrian
- ⇒ Sogdian 600BC
- ⇒ Mittani 1600BC (in Turkey)
- ⇒ Kassite 1500BC (Iraq?)
- ⇒ Proto-Baltic-Slavic 2800BC
- ⇒ Finns
- ⇒ Slavics
- ⇒ Rigvedic (?India) 1500BC?
Caucasus hunter gatherers origin theory
- new evidence suggests the Caucasus hunter gatherers were the origin of the Indo-European languages and they migrated north of the Caucasus and their WOMEN admixed with the Eastern European hunter gatherers
- this would support the “Noah and Mt Ararat” approach!
- supporting this is that there does not appear to be any steppe ancestry DNA in Hittites in Anatolia
- the modifications this theory then also makes are:
- that Greek came from Anatolia and this came from the Caucasus hunter gatherers before they migrated north
- Iran and thence Vedic came directly from the Caucasus hunter gatherers before they migrated north
- the male haplotype spread from the Caucasus region include:
- R1a (Indo-Iranian and Eastern European plus Nth Kazakhstan)
- R1b (Armenia and western Russia - Bashkir)
- J2 (Nth Middle Eastern) Iran, Turkey, west Palestine, Anatolia, Greece
- J2a (southern Italy, Sicily, Malta)
- J1E (Sth Middle Eastern / Semitic) to eastern Palestine, eastern Egypt and the whole Arabian Peninsula plus a segment near Tunis
- E3b1 (Egyptian)
- E3b2 (Berber - north Africa)
Paleoneurology
the cost of evolving the hominid brain
- an opposable thumb is a feature of primates which allows them to climb tree branches better, but hominids took this much further to evolve a fully opposable thumb with far more functionality
- but it is really the brain combined with bipedal gait to make the most use of this thumb that sets humans most apart from other species and the modern brain requires 20% of our blood supply and energy
- as the brain evolved larger and larger (modern brain is 3x the size of chimpanzees which is already larger than most other species in relation to body weight), these energy requirements were met any several ways and with a number of ramifications
- primates had evolved as hind gut fermenters and had diets consisting mainly of “C3” vegetation such as foliage from which they extracted the needed protein and energy by having to grind away eating for 50% of their waking hours and thus they had large molars and massive chewing muscles (masseters).
- in contrast, bovine animals were fore-gut fermenters and mainly ate “C4” vegetation such as grasses which has a different C12 :C13 ratio than C3 vegetation due to different enzyme systems used to process carbon.
- primates supplement with fruits in season but these whilst providing energy do not provide protein or fats and sometimes supplemented with raw meats (small primates ate insects for protein but this is inadequate for large primates)
- this raw vegetation and even raw meat was not sufficient to provide the energy and oxygen demands of the enlarging brain
- even now for adult women, if their diet was solely raw foods even if they included raw meat, the poor energy bioavailability of uncooked foods results in low BMI and 50% will have amenorrhoea - clearly this diet is NOT conducive to evolution if the species can't procreate efficiently
- at some point they would have discovered distal limb bone marrow and the brain were relatively safe to eat as not only did these have a higher fat content, but were less accessible to bacteria after death
- a key enabler for the early hominids was getting control of fire to cook, create smoke to given them access to honey, and to keep them warm at night. This was supplemented by the use of stone tools from as early as 3.3 million years ago thanks to early hands capable of limited throwing and clubbing, which perhaps drove evolution of the fully opposable thumb (perhaps 1mya with H. habilis and H.erectus) which then allowed powerful capability to throw objects and use clubs which were useful for hunting - by 500,000yrs ago, they had developed spears
- cooking foods increased bioavailability of energy by about 50% and markedly reduced the need for fermentative hind gut as less foods were passed undigested, this allowed the hind gut to be reduced in size and divert its blood flow to the brain, further allowing the brain to evolve in size.
- cooked foods meant that they needed to spend FAR less time chewing and eating and thus had far greater time to develop brain creativity and consider other activities
- critically, the ability to cook meant that meat could be rendered far safer to eat if it was starting to decay, less chance of acquiring an helminth infection, and no longer did they need to rely upon bone marrow alone or early kills
- red meat also was a far more effective source of iron which was increasingly critical for delivering oxygen to the brain as well as providing important nutrients such as critical unsaturated fatty acids which hominids can't synthesize for brain development and vitamins such as B12 which is essential for nerve development and functioning.
- the growing increased emphasis on meat drove them to become game hunters and various features needed to occur to enable this:
- bipedal gait allowing hands free to attack game
- ability to run and tolerate the hot African conditions compounded by an increasing hot brain needing cooling (the larger brain essentially became a 20W heater enclosed in bone) required losing their fur (the fur was no longer needed for warmth now that they could make fires to keep them warm at night) and evolving naked skin which could perspire, but this unprotected skin needed to also evolve deep melanin pigmentation to protect from UV radiation and increasing blood circulation to dissipate the heat from the brain as well as provide glucose and oxygen in high quantities (hence larger carotid arteries entering the skull).
- those species which migrated to regions with less UV evolved mechanism to either totally turn off melanin production to ensure vitamin D production (pale redheads), or to have a UV-responsive seasonal tanning capability (eg. olive skinned Mediterraneans)
Evolutionary changes of the cranium and brain size:
- 4 main evolutionary parts of the brain:
- pons, medulla & brainstem
- the most primitive structures of the brain
- these control autonomic functions such as breathing, heart functions & vital organ regulation
- innate instincts:
- 2 basic instincts which predate even Cambrian life forms and are DNA based:
- self-preservation
- hunger
- thirst
- fear of predators esp. spiders/reptiles/dinosaurs
- reproduction
- the R-complex
- evolved about 350 million yrs ago
- “Reptilian” but is actually originates from the early amphibians of the Devonian Period, & only later developed independently in reptiles, dinosaurs & mammals
- an extremely important development in that it allowed rudimentary intelligence & problem solving capability
- the basics of emotion developed along with the chemistry of instinct:
- 3 abstract innate instincts that require a brain & hence evolved later than the above 2:
- territorialism - fear of closed spaces - loss of territory
- social hierarchy
- ritualism
- limbic system:
- about 65 million yrs ago, at the end of the Cretaceous Period when dinosaurs and reptiles dominated, the small mammals developed the limbic system which contained most emotions & was pre-wired with basic instinct information beyond what DNA can supply elaborating on the innate instincts:
- self-preservation:
- fear of falling - when primates started climbing trees
- reproduction:
- fear of mating rejection
- neocortex:
- finally the 3rd, & most important development was the neocortex which is the seat of intelligence, human initiative & self awareness.
- the growth of the right side of the brain before the left is purely accidental & accompanied the evolution of higher mammals, esp. primates including man
- this allowed logic to over-ride immediate gratification of innate instincts
- further brain developments:
- development of increased frequencies of skull emissary foramina from in A. africanus to Homo sapiens to allow intracranial veins to communicate with extracranial veins and thus provide for a radiator control system to prevent over-heating of the brain in hot environments and on exertion which allowed the brain to increase in size beyond its previous thermal constraints.
- rearrangement of vascular system to brain to compensate for bipedal stature's gravitational effects in A. africanus
- brain size increased 3-fold from the modern chimpanzee sized brain of the bipedal australopithecine 2 million yrs ago to the modern Homo sapiens
- the volume of the neocortex is linearly proportional to the total brain volume and thus is relatively constant proportion for all anthropoid primates
- relative volume of white matter increases with brain size from 9% in pygmy marmosets to 34% in humans
- brain weight in relation to body weight of various species:
- the shrinking Y-chromosome:
- the current human Y chromosome consists of 45 genes, down from 1438 genes 300 million years ago
- the loss of the Y chromosome in many species has led to their extinction
- it is estimated that humans will lose the Y chromosome in 10 million years at the current rate.
- human fertility will decay to 1% of its present level in 125,000yrs
modern day micro-evolution
- 4500BC onwards, increasing infections from larger social groups such as norovirus, etc have resulted in survivors having more tendency to auto-immune diseases such as IBD
- the 14thC bubonic plagues in Europe killed 25 million people, almost half the population and would have impacted micro-evolution
- those with two versions of type A version of ERAP2 gene which better activated the immune system were 40% more likely to survive the plague and thus survivors are also more likely to have this allele
- this may have resulted in an increased prevalence of Crohn's disease which is associated with this allele
- researchers identified 3 other gene alleles associated with survival but these are alos associated with SLE and RhA
- prevalence of the presence of a persistent median artery in forearms into adulthood (this normally regresses in early fetal periods after 8wks gestation) appears to have tripled in those of European descent over the past 100 years
- prevalence of the fabella in the knee joint has tripled over the past 100 yrs
- reducing prevalence of wisdom teeth
history/ev_human.txt · Last modified: 2024/07/29 21:18 by gary1