For another billion years, prokaryotes would continue to diversify undisturbed.

The Holozoa lineage of eukaryotes evolves many features for making cell colonies, and finally leads to the ancestor of animals (metazoans) and choanoflagellates.^[5][6]

Proterospongia (members of the Choanoflagellata) are the best living examples of what the ancestor of all animals may have looked like. They live in colonies, and show a primitive level of cellular specialization for different tasks.

Urmetazoan: The first fossils that might represent animals appear in the 665-million-year-old rocks of the Trezona Formation of South Australia. These fossils are interpreted as being early sponges.^[7] Multicellular animals may have existed from 800 Ma. Separation from the Porifera (sponges) lineage. Eumetazoa/Diploblast: separation from the Ctenophora ("comb jellies") lineage. Planulozoa/ParaHoxozoa: separation from the Placozoa and Cnidaria lineages. All diploblasts possess epithelia, nerves, muscles and connective tissue and mouths, and except for placozoans, have some form of symmetry, with their ancestors probably having radial symmetry like that of cnidarians. Diploblasts separated their early embryonic cells into two germ layers (ecto- and endoderm). Photoreceptive eye-spots evolve.

Urbilaterian: the last common ancestor of xenacoelomorphs, protostomes (including the arthropod [insect, crustacean, spider], mollusc [squid, snail, clam] and annelid [earthworm] lineages) and the deuterostomes (including the vertebrate [human] lineage) (the last two are more related to each other and called Nephrozoa). Xenacoelomorphs all have a gonopore to expel gametes but nephrozoans merged it with their anus. Earliest development of bilateral symmetry, mesoderm, head (anterior cephalization) and various gut muscles (and thus peristalsis) and, in the Nephrozoa, nephridia (kidney precursors), coelom (or maybe pseudocoelom), distinct mouth and anus (evolution of through-gut), and possibly even nerve cords and blood vessels.^[8] Reproductive tissue probably concentrates into a pair of gonads connecting just before the posterior orifice. "Cup-eyes" and balance organs evolve (the function of hearing added later as the more complex inner ear evolves in vertebrates). The nephrozoan through-gut had a wider portion in the front, called the pharynx. The integument or skin consists of an epithelial layer (epidermis) and a connective layer.

Most known animal phyla appeared in the fossil record as marine species during the Ediacaran-Cambrian explosion, probably caused by long scale oxygenation since around 585 Ma (sometimes called the Neoproterozoic Oxygenation Event or NOE) and also an influx of oceanic minerals. Deuterostomes, the last common ancestor of the Chordata [human] lineage, Hemichordata (acorn worms and graptolites) and Echinodermata (starfish, sea urchins, sea cucumbers, etc.), probably had both ventral and dorsal nerve cords like modern acorn worms.

An archaic survivor from this stage is the acorn worm, sporting an open circulatory system (with less branched blood vessels) with a heart that also functions as a kidney. Acorn worms have a plexus concentrated into both dorsal and ventral nerve cords. The dorsal cord reaches into the proboscis, and is partially separated from the epidermis in that region. This part of the dorsal nerve cord is often hollow, and may well be homologous with the brain of vertebrates.^[9] Deuterostomes also evolved pharyngeal slits, which were probably used for filter feeding like in hemi- and proto-chordates.

The increased amount of oxygen causes many eukaryotes, including most animals, to become obligate aerobes.

The Chordata ancestor gave rise to the lancelets (Amphioxii) and Olfactores. Ancestral chordates evolved a post-anal tail, notochord, and endostyle (precursor of thyroid). The pharyngeal slits (or gills) are now supported by connective tissue and used for filter feeding and possibly breathing.^[10] Other, earlier chordate predecessors include Myllokunmingia fengjiaoa,^[11] Haikouella lanceolata,^[12] and Haikouichthys ercaicunensis.^[13] They probably lost their ventral nerve cord and evolved a special region of the dorsal one, called the brain, with glia becoming permanently associated with neurons. They probably evolved the first blood cells (probably early leukocytes, indicating advanced innate immunity), which they made around the pharynx and gut.^[14] All chordates except tunicates sport an intricate, closed circulatory system, with highly branched blood vessels.

Olfactores, last common ancestor of tunicates and vertebrates in which olfaction (smell) evolved. Since lancelets lack a heart, it possibly emerged in this ancestor (previously the blood vessels themselves were contractile) though it could have been lost in lancelets after evolving in early deuterostomes (hemichordates and echinoderms have hearts).

The first vertebrates ("fish") appear: the ostracoderms. Haikouichthys and Myllokunmingia are examples of these jawless fish, or Agnatha; the jawless Cyclostomata diverge at this stage. They were jawless, had seven pairs of pharyngeal arches like their descendants today, and their endoskeletons were cartilaginous (then only consisting of the chondrocranium/braincase and vertebrae). The connective tissue below the epidermis differentiates into the dermis and hypodermis.^[15] They depended on gills for respiration and evolved the unique sense of taste (the remaining sense of the skin now called "touch"), endothelia, camera eyes and inner ears (capable of hearing and balancing; each consists of a lagena, an otolithic organ and two semicircular canals) as well as livers, thyroids, kidneys and two-chambered hearts (one atrium and one ventricle). They had a tail fin but lacked the paired (pectoral and pelvic) fins of more advanced fish. Brain divided into three parts (further division created distinct regions based on function). The pineal gland of the brain penetrates to the level of the skin on the head, making it seem like a third eye. They evolved the first erythrocytes and thrombocytes.^[16]

The Placodermi were the first jawed fishes (Gnathostomata); their jaws evolved from the first gill/pharyngeal arch and they largely replaced their endoskeletal cartilage with bone and evolved pectoral and pelvic fins. Bones of the first gill arch became the upper and lower jaw, while those from the second arch became the hyomandibula, ceratohyal and basihyal; this closed two of the seven pairs of gills. The gap between the first and second arches just below the braincase (fused with upper jaw) created a pair of spiracles, which opened in the skin and led to the pharynx (water passed through them and left through gills). Placoderms had competition with the previous dominant animals, the cephalopods and sea scorpions, and rose to dominance themselves. A lineage of them probably evolved into the bony and cartilaginous fish, after evolving scales, teeth (which allowed the transition to full carnivory), stomachs, spleens, thymuses, myelin sheaths, hemoglobin and advanced, adaptive immunity (the latter two occurred independently in the lampreys and hagfish). Jawed fish also have a third, lateral semicircular canal and their otoliths are divided between a saccule and utricle.

Some freshwater lobe-finned fish (sarcopterygii) develop limbs and give rise to the Tetrapodomorpha. These fish evolved in shallow and swampy freshwater habitats, where they evolved large eyes and spiracles.

Primitive tetrapods ("fishapods") developed from tetrapodomorphs with a two-lobed brain in a flattened skull, a wide mouth and a medium snout, whose upward-facing eyes show that it was a bottom-dweller, and which had already developed adaptations of fins with fleshy bases and bones. (The "living fossil" coelacanth is a related lobe-finned fish without these shallow-water adaptations.) Tetrapod fishes used their fins as paddles in shallow-water habitats choked with plants and detritus. The universal tetrapod characteristics of front limbs that bend backward at the elbow and hind limbs that bend forward at the knee can plausibly be traced to early tetrapods living in shallow water.^[18]

Panderichthys is a 90–130 cm (35–50 in) long fish from the Late Devonian period (380 Mya). It has a large tetrapod-like head. Panderichthys exhibits features transitional between lobe-finned fishes and early tetrapods.

Trackway impressions made by something that resembles Ichthyostega's limbs were formed 390 Ma in Polish marine tidal sediments. This suggests tetrapod evolution is older than the dated fossils of Panderichthys through to Ichthyostega.

Tiktaalik is a genus of sarcopterygian (lobe-finned) fishes from the late Devonian with many tetrapod-like features. It shows a clear link between Panderichthys and Acanthostega.

Acanthostega is an extinct tetrapod, among the first animals to have recognizable limbs. It is a candidate for being one of the first vertebrates to be capable of coming onto land. It lacked wrists, and was generally poorly adapted for life on land. The limbs could not support the animal's weight. Acanthostega had both lungs and gills, also indicating it was a link between lobe-finned fish and terrestrial vertebrates. The dorsal pair of ribs form a rib cage to support the lungs, while the ventral pair disappears.

Ichthyostega is another extinct tetrapod. Being one of the first animals with only two pairs of limbs (also unique since they end in digits and have bones), Ichthyostega is seen as an intermediate between a fish and an amphibian. Ichthyostega had limbs but these probably were not used for walking. They may have spent very brief periods out of water and would have used their limbs to paw their way through the mud.^[19] They both had more than five digits (eight or seven) at the end of each of their limbs, and their bodies were scaleless (except their bellies, where they remained as gastralia). Many evolutionary changes occurred at this stage: eyelids and tear glands evolved to keep the eyes wet out of water and the eyes became connected to the pharynx for draining the liquid; the hyomandibula (now called columella) shrank into the spiracle, which now also connected to the inner ear at one side and the pharynx at another, becoming the Eustachian tube (columella assisted in hearing); an early eardrum (a patch of connective tissue) evolved on the end of each tube (called the otic notch); and the ceratohyal and basihyal merged into the hyoid. These "fishapods" had more ossified and stronger bones to support themselves on land (especially skull and limb bones). Jaw bones fuse together while gill and opercular bones disappear.

Pederpes from around 350 Ma indicates that the standard number of 5 digits evolved at the Early Carboniferous, when modern tetrapods (or "amphibians") split in two directions (one leading to the extant amphibians and the other to amniotes). At this stage, our ancestors evolved vomeronasal organs, salivary glands, tongues, parathyroid glands, three-chambered hearts (with two atria and one ventricle) and bladders, and completely removed their gills by adulthood. The glottis evolves to prevent food going into the respiratory tract. Lungs and thin, moist skin allowed them to breathe; water was also needed to give birth to shell-less eggs and for early development. Dorsal, anal and tail fins all disappeared.

Lissamphibia (extant amphibians) retain many features of early amphibians but they have only four digits (caecilians have none).

From amphibians came the first reptiles: Hylonomus is the earliest known reptile. It was 20 cm (8 in) long (including the tail) and probably would have looked rather similar to modern lizards. It had small sharp teeth and probably ate small millipedes and insects. It is a precursor of later amniotes (broadest sense of "reptile"). Alpha keratin first evolves here; it is used in the claws of modern amniotes, and hair in mammals, indicating claws and a different type of scales evolved in amniotes (complete loss of gills as well).^[20]

Evolution of the amniotic egg gives rise to the amniotes, tetrapods that can reproduce on land and lay shelled eggs on dry land. They did not need to return to water for reproduction nor breathing. This adaptation and the desiccation-resistant scales gave them the capability to inhabit the uplands for the first time, albeit making them drink water through their mouths. At this stage, adrenal tissue may have concentrated into discrete glands.

Amniotes have advanced nervous systems, with twelve pairs of cranial nerves, unlike lower vertebrates. They also evolved true sternums but lost their eardrums and otic notches (hearing only by columella bone conduction).

The earliest "mammal-like reptiles" are the pelycosaurs. The pelycosaurs were the first animals to have temporal fenestrae. Pelycosaurs were not therapsids but their ancestors. The therapsids were, in turn, the ancestors of mammals.

The therapsids had temporal fenestrae larger and more mammal-like than pelycosaurs, their teeth showed more serial differentiation, their gait was semi-erect and later forms had evolved a secondary palate. A secondary palate enables the animal to eat and breathe at the same time and is a sign of a more active, perhaps warm-blooded, way of life.^[21] They had lost gastralia and, possibly, scales.

One subgroup of therapsids, the cynodonts, lose pineal eye and lumbar ribs and very likely became warm-blooded. The lower respiratory tract forms intricate branches in the lung parenchyma, ending in highly vascularized alveoli. Erythrocytes and thrombocytes lose their nuclei while lymphatic systems and advanced immunity emerge. They may have also had thicker dermis like mammals today.

The jaws of cynodonts resembled modern mammal jaws; the anterior portion, the dentary, held differentiated teeth. This group of animals likely contains a species which is the ancestor of all modern mammals. Their temporal fenestrae merged with their orbits. Their hindlimbs became erect and their posterior bones of the jaw progressively shrunk to the region of the columella.^[22]

From Eucynodontia came the first mammals. Most early mammals were small shrew-like animals that fed on insects and had transitioned to nocturnality to avoid competition with the dominant archosaurs — this led to the loss of the vision of red and ultraviolet light (ancestral tetrachromacy of vertebrates reduced to dichromacy). Although there is no evidence in the fossil record, it is likely that these animals had a constant body temperature, hair and milk glands for their young (the glands stemmed from the milk line). The neocortex (part of the cerebrum) region of the brain evolves in Mammalia, at the reduction of the tectum (non-smell senses which were processed here became integrated into neocortex but smell became primary sense). Origin of the prostate gland and a pair of holes opening to the columella and nearby shrinking jaw bones; new eardrums stand in front of the columella and Eustachian tube. The skin becomes hairy, glandular (glands secreting sebum and sweat) and thermoregulatory. Teeth fully differentiate into incisors, canines, premolars and molars; mammals become diphyodont and possess developed diaphragms and males have internal penises. All mammals have four chambered hearts (with two atria and two ventricles) and lack cervical ribs (now mammals only have thoracic ribs).

Monotremes are an egg-laying group of mammals represented today by the platypus and echidna. Recent genome sequencing of the platypus indicates that its sex genes are closer to those of birds than to those of the therian (live birthing) mammals. Comparing this to other mammals, it can be inferred that the first mammals to gain sexual differentiation through the existence or lack of SRY gene (found in the y-Chromosome) evolved only in the therians. Early mammals and possibly their eucynodontian ancestors had epipubic bones, which serve to hold the pouch in modern marsupials (in both sexes).

Evolution of live birth (viviparity), with early therians probably having pouches for keeping their undeveloped young like in modern marsupials. Nipples stemmed out of the therian milk lines. The posterior orifice separates into anal and urogenital openings; males possess an external penis.

Monotremes and therians independently detach the malleus and incus from the dentary (lower jaw) and combine them to the shrunken columella (now called stapes) in the tympanic cavity behind the eardrum (which is connected to the malleus and held by another bone detached from the dentary, the tympanic plus ectotympanic), and coil their lagena (cochlea) to advance their hearing, with therians further evolving an external pinna and erect forelimbs. Female placentalian mammals do not have pouches and epipubic bones but instead have a developed placenta which penetrates the uterus walls (unlike marsupials), allowing a longer gestation; they also have separated urinary and genital openings.^[23]

A group of small, nocturnal, arboreal, insect-eating mammals called Euarchonta begins a speciation that will lead to the orders of primates, treeshrews and flying lemurs. They reduced the number of mammaries to only two pairs (on the chest). Primatomorpha is a subdivision of Euarchonta including primates and their ancestral stem-primates Plesiadapiformes. An early stem-primate, Plesiadapis, still had claws and eyes on the side of the head, making it faster on the ground than in the trees, but it began to spend long times on lower branches, feeding on fruits and leaves.

The Plesiadapiformes very likely contain the ancestor species of all primates.^[24] They first appeared in the fossil record around 66 million years ago, soon after the Cretaceous–Paleogene extinction event that eliminated about three-quarters of plant and animal species on Earth, including most dinosaurs.^[25][26]

One of the last Plesiadapiformes is Carpolestes simpsoni, having grasping digits but not forward-facing eyes.

Simians split into infraorders Platyrrhini and Catarrhini. They fully transitioned to diurnality and lacked any claw and tapetum lucidum (which evolved many times in various vertebrates). They possibly evolved at least some of the paranasal sinuses, and transitioned from estrous cycle to menstrual cycle. The number of mammaries is now reduced to only one thoracic pair. Platyrrhines, New World monkeys, have prehensile tails and males are color blind. The individuals whose descendants would become Platyrrhini are conjectured to have migrated to South America either on a raft of vegetation or via a land bridge (the hypothesis now favored^[27]). Catarrhines mostly stayed in Africa as the two continents drifted apart. Possible early ancestors of catarrhines include Aegyptopithecus and Saadanius.

Catarrhini splits into 2 superfamilies, Old World monkeys (Cercopithecoidea) and apes (Hominoidea). Human trichromatic color vision had its genetic origins in this period. Catarrhines lost the vomeronasal organ (or possibly reduced it to vestigial status).

Proconsul was an early genus of catarrhine primates. They had a mixture of Old World monkey and ape characteristics. Proconsul's monkey-like features include thin tooth enamel, a light build with a narrow chest and short forelimbs, and an arboreal quadrupedal lifestyle. Its ape-like features are its lack of a tail, ape-like elbows, and a slightly larger brain relative to body size.

Proconsul africanus is a possible ancestor of both great and lesser apes, including humans.

Pierolapithecus catalaunicus is thought to be a common ancestor of humans and the other great apes, or at least a species that brings us closer to a common ancestor than any previous fossil discovery. It had the special adaptations for tree climbing as do present-day humans and other great apes: a wide, flat rib cage, a stiff lower spine, flexible wrists, and shoulder blades that lie along its back.

Hominini: The latest common ancestor of humans and chimpanzees is estimated to have lived between roughly 10 to 5 million years ago. Both chimpanzees and humans have a larynx that repositions during the first two years of life to a spot between the pharynx and the lungs, indicating that the common ancestors have this feature, a precondition for vocalized speech in humans. Speciation may have begun shortly after 10 Ma, but late admixture between the lineages may have taken place until after 5 Ma. Candidates of Hominina or Homininae species which lived in this time period include Graecopithecus (c. 7 Ma), Sahelanthropus tchadensis (c. 7 Ma), Orrorin tugenensis (c. 6 Ma).

Ardipithecus was arboreal, meaning it lived largely in the forest where it competed with other forest animals for food, no doubt including the contemporary ancestor of the chimpanzees. Ardipithecus was probably bipedal as evidenced by its bowl shaped pelvis, the angle of its foramen magnum and its thinner wrist bones, though its feet were still adapted for grasping rather than walking for long distances.

A member of the Australopithecus afarensis left human-like footprints on volcanic ash in Laetoli, northern Tanzania, providing strong evidence of full-time bipedalism. Australopithecus afarensis lived between 3.9 and 2.9 million years ago, and is considered one of the earliest hominins—those species that developed and comprised the lineage of Homo and Homo's closest relatives after the split from the line of the chimpanzees.

It is thought that A. afarensis was ancestral to both the genus Australopithecus and the genus Homo. Compared to the modern and extinct great apes, A. afarensis had reduced canines and molars, although they were still relatively larger than in modern humans. A. afarensis also has a relatively small brain size (380–430 cm³) and a prognathic (anterior-projecting) face.

Australopithecines have been found in savannah environments; they probably developed their diet to include scavenged meat. Analyses of Australopithecus africanus lower vertebrae suggests that these bones changed in females to support bipedalism even during pregnancy.

Early Homo appears in East Africa, speciating from australopithecine ancestors. The Lower Paleolithic is defined by the beginning of use of stone tools. Australopithecus garhi was using stone tools at about 2.5 Ma. Homo habilis is the oldest species given the designation Homo, by Leakey et al. in 1964. H. habilis is intermediate between Australopithecus afarensis and H. erectus, and there have been suggestions to re-classify it within genus Australopithecus, as Australopithecus habilis.

LD 350-1 is now considered the earliest known specimen of the genus Homo, dating to 2.75–2.8 Ma, found in the Ledi-Geraru site in the Afar Region of Ethiopia. It is currently unassigned to a species, and it is unclear if it represents the ancestor to H. habilis and H. rudolfensis, which are estimated to have evolved around 2.4 Ma.^[36]

Stone tools found at the Shangchen site in China and dated to 2.12 million years ago are considered the earliest known evidence of hominins outside Africa, surpassing Dmanisi hominins found in Georgia by 300,000 years, although whether these hominins were an early species in the genus Homo or another hominin species is unknown.^[37]

Homo erectus derives from early Homo or late Australopithecus.

Homo habilis, although significantly different of anatomy and physiology, is thought to be the ancestor of Homo ergaster, or African Homo erectus; but it is also known to have coexisted with H. erectus for almost half a million years (until about 1.5 Ma). From its earliest appearance at about 1.9 Ma, H. erectus is distributed in East Africa and Southwest Asia (Homo georgicus). H. erectus is the first known species to develop control of fire, by about 1.5 Ma.

H. erectus later migrates throughout Eurasia, reaching Southeast Asia by 0.7 Ma. It is described in a number of subspecies.^[38] Early humans were social and initially scavenged, before becoming active hunters. The need to communicate and hunt prey efficiently in a new, fluctuating environment (where the locations of resources need to be memorized and told) may have driven the expansion of the brain from 2 to 0.8 Ma.

Evolution of dark skin at about 1.2 Ma.^[39]

Homo antecessor may be a common ancestor of humans and Neanderthals.^[40][41] At present estimate, humans have approximately 20,000–25,000 genes and share 99% of their DNA with the now extinct Neanderthal^[42] and 95–99% of their DNA with their closest living evolutionary relative, the chimpanzees.^[43][44] The human variant of the FOXP2 gene (linked to the control of speech) has been found to be identical in Neanderthals.^[45]

Divergence of Neanderthal and Denisovan lineages from a common ancestor.^[46] Homo heidelbergensis (in Africa also known as Homo rhodesiensis) had long been thought to be a likely candidate for the last common ancestor of the Neanderthal and modern human lineages. However, genetic evidence from the Sima de los Huesos fossils published in 2016 seems to suggest that H. heidelbergensis in its entirety should be included in the Neanderthal lineage, as "pre-Neanderthal" or "early Neanderthal", while the divergence time between the Neanderthal and modern lineages has been pushed back to before the emergence of H. heidelbergensis, to about 600,000 to 800,000 years ago, the approximate age of Homo antecessor.^[47][48] Brain expansion (enlargement) between 0.8 and 0.2 Ma may have occurred due to the extinction of most African megafauna (which made humans feed from smaller prey and plants, which required greater intelligence due to greater speed of the former and uncertainty about whether the latter were poisonous or not), extreme climate variability after Mid-Pleistocene Transition (which intensified the situation, and resulted in frequent migrations), and in general selection for more social life (and intelligence) for greater chance of survival, reproductivity, and care for mothers. Solidified footprints dated to about 350 ka and associated with H. heidelbergensis were found in southern Italy in 2003.^[49]

H. sapiens lost the brow ridges from their hominid ancestors as well as the snout completely, though their noses evolve to be protruding (possibly from the time of H. erectus). By 200 ka, humans had stopped their brain expansion.

Neanderthals and Denisovans emerge from the northern Homo heidelbergensis lineage around 500-450 ka while sapients emerge from the southern lineage around 350-300 ka.^[50]

Fossils attributed to H. sapiens, along with stone tools, dated to approximately 300,000 years ago, found at Jebel Irhoud, Morocco^[51] yield the earliest fossil evidence for anatomically modern Homo sapiens. Modern human presence in East Africa (Gademotta), at 276 kya.^[52] In July 2019, anthropologists reported the discovery of 210,000 year old remains of what may possibly have been a H. sapiens in Apidima Cave, Peloponnese, Greece.^[53][54][55]

Patrilineal and matrilineal most recent common ancestors (MRCAs) of living humans roughly between 200 and 100 kya^[56][57] with some estimates on the patrilineal MRCA somewhat higher, ranging up to 250 to 500 kya.^[58]

160,000 years ago, Homo sapiens idaltu in the Awash River Valley (near present-day Herto village, Ethiopia) practiced excarnation.^[59]

Modern human presence in Southern Africa and West Africa.^[60] Appearance of mitochondrial haplogroup (mt-haplogroup) L2.

Early evidence for behavioral modernity.^[61] Appearance of mt-haplogroups M and N. Southern Dispersal migration out of Africa, Proto-Australoid peopling of Oceania.^[62] Archaic admixture from Neanderthals in Eurasia,^[63][64] from Denisovans in Oceania with trace amounts in Eastern Eurasia,^[65] and from an unspecified African lineage of archaic humans in Sub-Saharan Africa as well as an interbred species of Neanderthals and Denisovans in Asia and Oceania.^{[66][67][68][69]}

Behavioral modernity develops by this time or earlier, according to the "great leap forward" theory.^[70] Extinction of Homo floresiensis.^[71] M168 mutation (carried by all non-African males). Appearance of mt-haplogroups U and K. Peopling of Europe, peopling of the North Asian Mammoth steppe. Paleolithic art. Extinction of Neanderthals and other archaic human variants (with possible survival of hybrid populations in Asia and Africa). Appearance of Y-Haplogroup R2; mt-haplogroups J and X.

Last Glacial Maximum; Epipaleolithic / Mesolithic / Holocene. Peopling of the Americas. Appearance of: Y-Haplogroup R1a; mt-haplogroups V and T. Various recent divergence associated with environmental pressures, e.g. light skin in Europeans and East Asians (KITLG, ASIP), after 30 ka;^[72] Inuit adaptation to high-fat diet and cold climate, 20 ka.^[73]

Extinction of late surviving archaic humans at the beginning of the Holocene (12 ka). Accelerated divergence due to selection pressures in populations participating in the Neolithic Revolution after 12 ka, e.g. East Asian types of ADH1B associated with rice domestication,^[74] or lactase persistence.^[75][76] A slight decrease in brain size occurred a few thousand years ago.^{[citation needed]}