This article is about the timeline of human evolution. For a
timeline of general evolution see Timeline of evolution.
See also Human
evolution for more details on this topic.
Evolutionary
tree
The timeline of
human evolution outlines the major events in the development of human species, and the evolution of
humans' ancestors.
It includes a brief explanation of some animals, species or genera, which are
possible ancestors of Homo sapiens sapiens. It does not address
the origin
of life, which is addressed by abiogenesis,
but presents a possible line of descendants that led to humans. This timeline
is based on studies from paleontology, developmental biology, morphology and from anatomical
and genetic
data. The study of human evolution is a major component of anthropology.
Contents
[hide] |
Date |
Event |
4000 Ma |
The earliest life appears. Further information: Origin
of life |
3900 Ma |
Cells resembling prokaryotes
appear. Further information: Cell (biology)#Origins of cells |
2500 Ma |
First organisms to utilize oxygen. |
2100 Ma |
More complex cells appear: the eukaryotes.
Further information: Eukaryote#Origin and evolution |
1200 Ma |
Sexual reproduction evolves,
leading to faster evolution.[1] |
900 Ma |
The choanoflagellates may look similar to the ancestors
of the entire animal
kingdom, and in particular they may be the
direct ancestors of sponges.[2]
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. |
600 Ma |
It is thought that the earliest multicellular animal was a
sponge-like
creature. Sponges are
among the simplest of animals, with partially differentiated tissues. Sponges (Porifera) are the phylogenetically oldest animal phylum extant
today. |
580 Ma |
The movement of all animals may have started with cnidarians.
Almost all cnidarians possess nerves and muscles and, because they are the simplest animals to
possess it, their direct ancestors were very likely the first animals to use nerves
and muscles together. Cnidarians are also the first animals with an actual body of definite form
and shape. They have radial symmetry. |
550 Ma |
Flatworms are the earliest animals to have a brain, and the
simplest animals alive to have bilateral symmetry. They are also the simplest
animals with organs that form from three germ layers. |
540 Ma |
Acorn worms are considered more highly specialised
and advanced than other similarly shaped worm-like creatures.
They have a circulatory system with a heart that also
functions as a kidney.
Acorn worms have a gill-like
structure used for breathing, a structure similar to that of primitive
fish. Acorn worms are thus sometimes said to be a link between vertebrates
and invertebrates[citation needed]. |
Date |
Event |
530 Ma |
One of the earliest known ancestor of the chordates
is Pikaia.[3]
It is the first known animal with a notochord.
Pikaia is believed to be the ancestor of all chordates
and vertebrates.[4]
The Lancelet,
still living today, retains some characteristics of the primitive chordates. It
resembles Pikaia Other earliest known chordate-like fossils is from a conodonts
an "eel-shaped animal of 4-20 cm (1½-8 in) long" with a
pair of huge eyes at the head end and a complex basket of teeth. |
505 Ma |
The first vertebrates appear: the ostracoderms,
jawless fish related to present-day lampreys and hagfishes. Haikouichthys
and Myllokunmingia are examples of these jawless
fish, or Agnatha.
(See also prehistoric fish). They were jawless and their
internal skeletons were cartilaginous. They lacked the paired (pectoral and
pelvic) fins of
more advanced fish.
They were the Precursors to the bony fish.
[5] |
480 Ma |
The Placodermi
were prehistoric fishes. Placoderms were the first of
the jawed fishes, their jaws evolving from the first of their gill arches [6].
Their head and thorax were covered by articulated armoured plates and the
rest of the body was scaled or naked. |
400 Ma |
First Coelacanth appears; this order of animals had been
thought to have no extant members until living specimens were discovered in
1938. It is often referred to as a living
fossil. |
375 Ma |
Tiktaalik is a genus of sarcopterygian
(lobe-finned) fishes from the late Devonian with many tetrapod-like features. |
Date |
Event |
365 Ma |
Some fresh water lobe-finned fish (Sarcopterygii) develop legs and give rise to the Tetrapoda. The first tetrapods evolved in shallow and swampy freshwater
habitats. Primitive tetrapods developed from a lobe-finned
fish (an "osteolepid Sarcopterygian"),
with a two-lobed brain
in a flattened skull, a wide mouth and a short 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. These 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.[7] Panderichthys
is a 90-130 cm (35-50 in) long fish from the Late Devonian
period. It has a large tetrapod-like head. Panderichthys exhibits features transitional between lobe-finned
fishes and early tetrapods. Lungfishes
retain some characteristics of the early Tetrapodas.
One example is the Australian Lungfish. |
315 Ma |
Acanthostega
is an extinct amphibian, 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. Ichthyostega
is an early tetrapod.
Being one of the first animals with legs, arms, and finger bones, Ichthyostega
is seen as a hybrid between a fish and an amphibian. Ichthyostega'
had legs but its limbs probably weren't used for walking, they
may have spent very brief periods out of water and would have used their legs
to paw their way through the mud.[8] Amphibia
were the first four-legged animals to develop lungs. Amphibians
living today still retain many characteristics of the early tetrapods. |
300 Ma |
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 millipedes
and early insects.
It is a precursor of later amniotes and mammal-like reptiles. Evolution of the amniotic egg gives rise to the Amniota, reptiles that
can reproduce on land and lay eggs on dry land. They did not need to return
to water for reproduction. This adaptation gave them the capability to
colonize the uplands for the first time. Reptiles have advanced nervous system, compared to amphibians.
They have twelve pairs of cranial nerves. |
Date |
Event |
256 Ma |
Phthinosuchus, an early Therapsid Shortly after the appearance of the first reptiles, two
branches split off. One branch is the Diapsida from
which come the modern reptiles. The other branch is Synapsida
which had temporal fenestra, a pair of holes in their
skulls behind the eyes, which were used to increase the space for jaw
muscles. The earliest mammal-like reptiles are the pelycosaurs.
The pelycosaurs were the first animals to have temporal fenestra. Pelycosaurs
are not Therapsida
but soon they gave rise to them. The Therapsida are the direct ancestor of mammals. The therapsids have temporal fenestrae larger and more mammal-like than
pelycosaurs, their teeth show more serial differentiation; 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. [9] |
220 Ma |
One sub-group of therapsids, the cynodonts
evolved more mammal-like characteristics. The jaws of cynodonts resemble modern mammal jaws. It is very likely this
group of animals contains a species which is the direct ancestor of all
modern mammals.[10] |
220 Ma |
From eucynodonts
(cynodonts)
came the first mammals.
Most early mammals were small and shrew-like animals that fed on insects.
Although there is no evidence in the fossil record, it is likely that these
animals had a constant body temperature, milk glands for their young. The neocortex
region of the brain
first evolved in mammals and thus is unique to them. |
125 Ma |
Eomaia scansoria, a eutherian mammal, leads
to the formation of modern placental mammals. It looks like modern dormouse,
climbing small shrubs in Liaoning, China. |
100 Ma |
Common genetic ancestor of mice and humans (base of the clade Euarchontoglires). |
Date |
Event |
65–85 Ma |
A Plesiadapis without fur. A group of small, nocturnal and arboreal, insect-eating mammals called the
Euarchonta
begins a speciation that will lead to the primate, treeshrew
and flying
lemur orders. The Primatomorpha is a
subdivision of Euarchonta that includes the primates and the proto-primate Plesiadapiformes.
One of the early proto-primates is Plesiadapis.
Plesiadapis still had claws and the eyes located on each side of the
head. Because of this they were faster on the ground than on the top of the
trees, but they began to spend long times on lower branches of trees, feeding
on fruits and leaves. The Plesiadapiformes
very likely contain the species which is the ancestor of all primates.[11] One of the last Plesiadapiformes is Carpolestes simpsoni. It had grasping
digits but no forward facing eyes. |
47 Ma |
Darwinius masillae, a transitional form between the prosimians
(lemurs and
other primitive primates) and the simians (monkeys, apes). It looked much
like a lemur but
had opposable thumbs. |
40 Ma |
Primates diverge into suborders Strepsirrhini
(wet-nosed primates) and Haplorrhini (dry nosed primates). Strepsirrhini
contains most of the prosimians; modern examples include the lemurs and lorises. The
haplorrhines include the three living groups the prosimian tarsiers, the
simian monkeys,
and apes. One of the
earliest haplorrhines is Teilhardina asiatica,
a mouse-sized, diurnal creature with small eyes. The Haplorrhini metabolism
lost the ability to make its own Vitamin C.
This means that it and all its descendants had to include fruit in its diet,
where Vitamin C could be obtained externally. |
30 Ma |
Haplorrhini
splits into infraorders Platyrrhini and Catarrhini.
Platyrrhines, New World monkeys, have prehensile tails and males are color
blind. They may have migrated to South America on a raft of vegetation across
the Atlantic ocean (circa 4,500 km, 2,800 mi). Catarrhines mostly
stayed in Africa
as the two continents drifted apart. One ancestor of catarrhines might be Aegyptopithecus. |
25 Ma |
Catarrhini
splits into 2 superfamilies, Old
World monkeys (Cercopithecoidea) and apes (Hominoidea). 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, and humans. |
Date |
Event |
15 Ma |
Hominidae (great apes) speciate from the ancestors of the
gibbon (lesser
apes). |
13 Ma |
Homininae ancestors speciate from the ancestors of the orangutan[12].
Pierolapithecus catalaunicus is
believed to be a common ancestor of humans and the great apes or
at least a species that brings us closer to a common ancestor than any
previous fossil
discovery. Pierolapithecus had special adaptations for tree climbing, just as
humans and other great apes do: a wide, flat ribcage, a
stiff lower spine, flexible wrists, and shoulder
blades that lie along its back. |
10 Ma |
|
7 Ma |
Hominina
speciate from the ancestors of the chimpanzees.
The latest common ancestor lived around the
time of Sahelanthropus tchadensis, ca. 7 Ma[2]; S. tchadensis is sometimes claimed to be the last
common ancestor of humans and chimpanzees, but this is disputed. The earliest
known human ancestor post-dating the separation of the human and the
chimpanzee lines is Orrorin tugenensis (Millennium Man, Kenya;
ca. 6 Ma). 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 precursor of
speech. |
4.4 Ma |
Ardipithecus is a very early hominin genus (subfamily Homininae).
Two species are described in the literature: A. ramidus, which lived
about 4.4 million years ago[13]
during the early Pliocene, and A. kadabba, dated to approximately
5.6 million years ago[14]
(late Miocene).
A. ramidus had a small brain, measuring between 300 and 350 cm3.
This is about the same size as modern bonobo and female
common chimpanzee brain, but much smaller than
the brain of australopithecines like Lucy (~400 to 550 cm3) and
slightly over a fifth the size of the modern Homo sapiens brain.
Ardipithecus was aboreal, meaning it lived largely in the forest where it
competed with other forest animals for food, including the contemporary
ancestor for the chimpanzees. |
3.6 Ma |
Some Australopithecus afarensis left
footprints on volcanic ash in Laetoli, Kenya (Northern Tanzania) Strong
evidence of bipedalism. Australopithecus afarensis lived between 3.9 and 2.9
million years ago. 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 has reduced canines and molars, although
they are still relatively larger than in modern humans. A. afarensis also has
a relatively small brain size (~380-430cm³) and a prognathic (i.e. projecting
anteriorly) face. Australopithecines have been found in Savannah environments
and likely increased its diet to include meat from scavenging opportunities.
An analysis of Australopithecus africanus lower vertebrae
suggests that females had changes to support bipedalism even while pregnant. |
3.5 Ma |
Kenyanthropus platyops, a possible
ancestor of Homo, emerges from the Australopithecus genus. |
3 Ma |
The bipedal australopithecines
(a genus of the Hominina subtribe) evolve in the savannas of Africa being
hunted by Dinofelis. Loss of body hair
takes place in the period 3-2 Ma, in parallel with the development of full bipedalism. |
Date |
Event |
2.5 Ma |
Appearance of Homo. Homo
habilis is thought to be the ancestor of the lankier and more
sophisticated Homo ergaster. Lived side by side with Homo
erectus until at least 1.44 Ma, making it highly unlikely that Homo
erectus directly evolved out of Homo
habilis. First stone tools, beginning of the Lower Paleolithic. Further information: Homo
rudolfensis |
1.8 Ma |
A reconstruction of Homo
erectus. Homo
erectus evolves in Africa. Homo erectus would bear a striking
resemblance to modern humans, but had a brain about 74 percent of the size of
modern man. Its forehead is less sloping and the teeth are smaller. Other
hominid designations such as Homo
georgicus, Homo ergaster, Homo
pekinensis, Homo heidelbergensis are often put under the
umbrella species name of Homo erectus[15].
Starting with Homo georgicus found in what is now the Republic of Georgia
dated at 1.8 Ma, the pelvis and backbone grew more human-like and gave
georgicus the ability cover very long distances in order to
follow herds of other animals. This is the oldest fossil of a hominid found
(so far) outside of Africa. Control of fire by early humans
is achieved 1.5 Ma by Homo ergaster. Homo ergaster reaches a height of around
1.9 metres (6.2 ft). Evolution of dark skin,
which is linked to the loss of body hair in human ancestors, is complete by
1.2 Ma. Homo pekinensis first appears in Asia around 700 Ka but according to
the "recently out of africa"
theory could not be a human ancestor, but rather, is just a cousin offshoot
species from Homo ergaster. Homo heidelbergensis was a very large hominid
that had a more advanced complement of cutting tools and
may have hunted big game such as horses. |
516 ka |
Homo antecessor is the common genetic
ancestor of humans and Neanderthal.[16]
At present estimate, humans have approximately 20,000–25,000 genes and share 99%
of their DNA with
the now extinct
Neanderthal
[17]
and 95-99% of their DNA
with their closest living evolutionary relative, the chimpanzees[18][19].
The human variant of the FOXP2 gene (linked to the control of speech) has been found
to be identical in Neanderthal[20].
It can therefore be deduced that Homo antecessor would also have had the
human FOXP2 gene. |
355 ka |
Three 1.5 m (5 ft) tall Homo heidelbergensis left footprints in powdery volcanic ash solidified in
Italy. Homo heidelbergensis is the common ancestor of both Homo neanderthalensis and Homo
sapiens. It is morphologically very similar to Homo
erectus but Homo heidelbergensis had a larger brain-case,
about 93% the size of that of Homo sapiens. The species was tall,
1.8 m (6 ft) on average, and more muscular than modern humans.
Beginning of the Middle Paleolithic. |
195 ka |
Homo sapiens sapiens (Pioneer
plaque) Omo1,
Omo2
(Ethiopia, Omo river) are the earliest fossil evidence for archaic Homo sapiens, evolved from Homo heidelbergensis. |
160 ka |
Homo sapiens (Homo sapiens idaltu) in Ethiopia, Awash
River, Herto village, practice mortuary rituals and butcher hippos. |
150 ka |
Mitochondrial Eve is a woman that lived in East
Africa. She is the statistically expected most recent female ancestor
common to all mitochondrial lineages in humans alive today. Note
that there is no evidence of any characteristic or genetic drift that
significantly differentiated her from the contemporary social group she lived
with at the time. Her ancestors were homo sapiens and her mother had the same
mtDNA. |
70 ka |
Appearance of mitochondrial haplogroup L2. Behavioral modernity. |
60 ka |
Y-chromosomal Adam lives in Africa. He is the most recent common ancestor from whom
all male human Y chromosomes are descended. Appearance of mitochondrial
haplogroups M and N, which participate in the migration out of Africa. |
50 ka |
Migration to South Asia. M168 mutation (carried by all non-African
males). Beginning of the Upper Paleolithic. mt-haplogroups U, K. |
40 ka |
Migration to Australia and Europe (Cro-Magnon). |
25 ka |
Neanderthals die out.
Y-Haplogroup R2; mt-haplogroups J, X. |
Beginning of the Mesolithic
/ Holocene.
Y-Haplogroup R1a; mt-haplogroups V, T. Evolution of light skin
in Europeans (SLC24A5).
Homo floresiensis dies out, leaving Homo
sapiens as the only living species of the genus Homo. |
|
Beginning of the Neolithic /
Holocene.
The invention of farming in the Fertile
Crescent occurred during this time. |