ANTH 1 Final Study Guide
Advantages
more energetically efficient than quadrupedal locomotion
frees hands for other uses
allows for improved long-distant vision
upright primates dissipate heat better than quadrupeds
Disadvantages
bipedal hominins are slower than their quadruped relatives
terrestrial living makes primates vulnerable to predation
early hominins would not seem to have had the size, intelligence, or cultural attributes to consistently offset this advantage
likely arose in a forest environment
early hominins likely would have needed to ascend trees at night to survive
believed it emerged as hominins shifted from fruit and leaf-based diets to one based around meat
saw the small canines of hominins as evidence that they were eating far fewer foods that need to be sliced and shredded
hominins adopted a hunting lifeway that created selective pressures for freeing up hands for creating tools
turned out to be wrong as data now shows that hominins only began regularly hunting and creating tools much later in their evolution
small brain sizes of the first hominins also show they likely lacked the cognitive abilities to be successful hunters
Stated that Africa was likely homeland to the first hominins
views were based on anatomical similarities between modern humans and African apes
reasoned that if our closest common living ancestors are Africa, so are our last common ancestors.
Patchy Forests
forests would have been reduced in size and density during dry periods
forest primates would have a selective advantage
Standing Feeding
arboreal mammals have difficulty feeding while gathering food in the trees so they often take their food to more stable branches or the ground
it has been hypothesized that bipeds in arboreal situations could be more comfortable eating in these areas
could have improved their energy allocation
Provisioning Hypothesis
proposed that bipedality may have emerges as part of an adaption where males provisioned females
males bringing them food improved energy allocation and allowed them to have more than one offspring at a time
implies monogamous relationships between males and females
also implies that there are selective advantages for males
these early hominin groups likely had social mechanisms that monitored behavior and promoted such male-female relationships
Canine Reduction
canine reduction is evidence of pair-bonded relationships
canines in all modern and fossil male apes are quite large and protruding and are used for fighting with or intimidating other males over sexual access to females
the earliest known hominin fossils show a marked reduction in canine size, compared to apes
Estrus Loss
modern female apes features an estrus cycle
refers when their genital region becomes swollen and discolored during ovulation
generally the only time when they are sexually receptive
modern humans have lost this estrus cycle
Lovejoy hypothesizes that this loss occurred at the beginning of hominin evolution to help promote pair-bonding
located in Africa
the result of faulting which has exposed millions of years of geologic strata
has featured regular volcanic activity for millions of years
allows for the application of Potassium-Argon dating methods
Sahelanthropus tchadensis
found in the northern desert of Chad
today this area is a grassland but data shows it was a swampy forest 7-6 MYA
holds some hominin features and some ape-like ones
was about the size of chimp and has a 350cc brain (small brain)
features a large supraorbital torus (brow ridge)
foramen magnum seemed to be positioned like that of a biped but could have been moved due to the skull being crushed and reformed
small canines and thick enamel on its molars
lack of shearing complex
flat face suggests it is not on the direct evolutionary lien to modern humans
Orrorin tugenensis
found near Lake Turkana, Kenya, in the Rift Valley
thick enamel on the molars
relatively large, ape-like canines
length and curvature of its femurs consistent with hominins
Ardipithecus ramidus
found in the Middle Awash river valley of Ethiopia (upper Rift Valley) by a team led by Timothy White
likely lived in a dense woodland but this area is now a desert
seems to have been both terrestrial and arboreal
45% of an individual skeleton has been found
about the size of a chimpanzee
brain in the low 400cc range
jutting lower face
grasping big toe (hallux)
foot has less-flexible muscularity typical of bipeds
hands and wrists are not anatomically designed for knuckle walking
does not feature evidence of brachiator anatomy
ape-like thin molar enamel
reduced canines
not much a shearing complex
lacking canine dimorphism between sexes
teeth feature thicker enamel than apes, but thinner than other hominins
Ardipithecus ramidus kadabba
found in the same region as the former and was likely its ancestor by a team led by Johannes Haile-Selassie
featured canine reduction but not to the same degree as A. ramidus
remains show a strong overall affinity with A. ramidus
Australopithecines
term coined by South African anatomist Raymond Dart
means “Southern Ape”
genus first discovered in the early 1920s in South Africa
numerous species have since been discovered in eastern and southern Africa though have never been found outside of Africa, like earlier hominins
all roughly within the size range of modern chimpanzees and bonobos
feature considerable sexual dimorphism
brain sizes range from the low to mid-400cc range
their feed do not have opposable big toes — closer to modern human feet than those of apes
still feature the following ape-like traits:
long, curved finger phalanges
shoulder joints still designed for suspensory locomotion
significant brow ridges
long arms
large teeth
ape-like hyoid bones
pyramid-shaped trapezoids
may have been regional creatures that spent time in the trees
exploited both forested and more open environments
practiced a mixed strategy likely of plant gathering, scavenging, and hunting of small game
likely made tools — most of which were made with materials, such as wood, that have not survived archaeologically
stone tools have been found dating back as far as 3.4 MYA+ which seem to have been used for digging and food processing as opposed to hunting
Australopithecus anamensis (4.0 MYA)
found in Kenya (Lake Turkana) by Maeve Leakey
Tim White believes it is a direct descendant of A. ramidus
has strong affinities with Au. afarensis
lived in a woodland environment
large molar with thick enamel
large canines and a slight shearing complex
ape-like u-shaped mandible
potentially featured canine dimorphism
sexual dimorphism in regard to body size
Australopithecus afarensis
discovered in 1974 by Don Johanson’s team at Hadar in Ethiopia
about the size of a chimp
avg. height for females is 3.5 and 4.9 feet for males
males potentially weighed twice as much as females
brain was in the 400cc range
features pronounced lower-face prognathism
lack opposable big toes and have very human-like feet
dental palate is less u-shaped compared to earlier hominins
large mandibles and teeth
thick enamel on molars
small canines and little canine dimorphism
except in regard to their size, teeth are more like later hominins than apes
first hominin species that lived in areas other than forests
seem to have occupied patchy woodlands, and open savannas
their teeth show a wide variety of wear patterns, indicating broad diets
large tooth and mandible size might have developed to eat hard foods found outside of forests
Australopithecus deyiremeda(3.5 - 3.3 MYA)
discovered by Yohannes Haile-Selassie in the Afar region of Ethiopia
strong affinities with Au. afarensis
very small teeth, which fall far outside the range of any other member of its genus
lived in woodlands and open areas
Australopithecus africanus ()
first reported by Raymond Dart in 1925
only found in southern African
potentially a direct descendant of Au afarensis
likely gave rise to other australopithecine species
may not be on the direct evolutionary line of humans
similar in size to A. afarensis
weighed between 65-95 lbs.
seems to be sexually dimorphic in regard to size
larger brains than earlier australopithecines (the mean being 454 cc)
less prognathic than A. afarensis
smaller, less specialized teeth than A. afarensis
“Taung Child” / Adult Au. africanus
Robust Australopithecines (2.5 - 1.3 MYA)
alternate genus = Paranthropus
found in southern and east Africa
arose from and have strong affinities with Au. africanus
roughly the same size as other australopithecines
brain size is in the 450cc range
extremely anatomically specialized
feature highly developed muscles of mastication
postorbital constriction, flares zygomatic arches; pronounces sagittal crests
chewing apparatus might be an adaption to harder, more fibrous foods
tooth-wear patterns in some individuals support this hypothesis
C4 analysis shows that at least one species (Au. boisei) specialized in eating grass
includes three difference species (that have been discovered)
Au. (P.) aethiopicus (2.6-2.5 MYA)
Au. (P.) boisei (2.3-1.2 MYA)
Au. (P.) robustus (2.0-1.5 MYA)
Au. aethiopicus and Au. boisei have only been found in eastern Africa whereas Au. robustus has only been found in southern Africa
Kenyanthropus platyops (“Flat face” — 3.5 MYA)
found by Maeve Leakey’s team in the region west of Lake Turkana (Kenya) in the late 1990s
seems to have lived in a woodland environment
small teeth and relatively flat face suggest that it is not an australopithecine
Australopithecus sediba (2.0-1.5 MYA)
found in the Malapa cave site in South Africa by American anthropologist Lee Berger in 2008
share features with both A. africanusand members of the genus Homo
features a 420cc-sized brain
tooth size similar to Homo, but design is more like A. africanus
pelvic shape similar to Homo, but foot structure similar to A. africanus
does not seem to be closely related to Au. robustus
Berger believes Au. sediba to be a link between the A. africanus and the genus Homo
others simply see parallel evolution at work and believe this species as another evolutionary dead end and their south African location relatively recent position in time would seem to go against their being a direct ancestor to our genus
Australopithecus garhi (“Surprise” — 2.5 MYA)
found in Ethiopia in 1999 by Ethiopian anthropologist Berhane Asfaw
upper limbs resemble those of A. afarensis, while lower limbs look like those of later hominins
leg and arm ratios are similar to later hominins
large premolars and molars (larger than the robust species)
large incisors
shares primitive facial and palate traits with Au. afarensis — large molars with thick enamel, relatively large canines, prognathic face, etc.
has 455cc brain size
primitive stone tools and animal bones with cut marks dating to the same period of Au. garhi have been in the region where this hominin lived
no other hominin find has been made in this region
early members of the genus homo made stone tools in this area
it’s geography, timing, and potential tool use make Au. garhi a strong candidate for a direct ancestor to the genus Homo
Climate
Ice sheets at the north and south poles (3 MYA - The Pliocene).
The Earth in general was cooling and drying at this time.
Glacial conditions become severe around 2.5 MYA.
The beginning of the Pleistocene (1.8 MYA) was a time of great climatic change. Yearly temperatures often fluctuated considerably, as did seasonal patterns.
Created unstable mosaic environments, which featured forests, patchy woodlands, savannas, and deserts.
Many species went extinct and new ones appeared — including primates/hominins.
Created strong selective pressures for intelligence and therefore increased socio-cultural abilities. The advantage would have gone to thsoe who could consistently live in multiple types of environments. Efficient longer-distance mobility may have been a key component.
Discovered in the early 1960s by Louis and Mary Leaky.
First found at Oldulvai Gorge in Tanzania, remains of a hominin dating to 2.5. MYA.
There are great differences in size within the members of this classification.
Certain very “robust” individuals have been found.
Some researchers believe these individuals are of a different species and have been classified as Homo rudolfensis. Others see this as an example of sexual dimorphism.
Remains are very fragmented and some researchers believe they are the remains of late-occurring members of a robust australopithecine species.
General Traits | Anatomical Changes (Compared to earlier hominins)
Males on average were 4.3 feet tall and females averaged 3.2 feet (similar to bonobos).
Males weight averaged 81 lbs. and females 70 lbs.
Brain sizes range form 503-661 cc, with a mean of 601 cc.
Still featured traits associated with autralopithecines (such as their general lower-body design).
Hand anatomy suggests that they had a more precise grips and greater manual dexterity.
Larger, more rounded brain-case.
Smaller, less jutting face.
Smaller post-canine teeth and large incisors.
Smaller chewing muscles
More efficient in their bidpedalism.
Seem to display greater intelligence.
Consist of flakes, cores, and hammer stones,
Flakes were used for slicing hides, butchering meat, and processing plant foods.
Cores are the stone from which flakes are “knocked off".”
Hammer stones were used to crack bone and to knock flakes off of cores.
Do not seem to be significantly specialized. They are used for roughly 2 MYA and change little throughout this period.
Some regional variation eventually develops within the industry. These tools will eventually be used by later hominin species.
H. habilis Lifeways — Hunters?
Meat becomes more important in hominin diets — evidence shots that early Homo butchered animals, often large ones.
Olduwan tools do not seem to be designed for hunting and appear to primarily be primitive processing tools.
Cognitive abilities and social structures also may not have been sufficient for them to live entirely by a hunting lifeway.
Behavioral ecology models show the most optimal lifeway would have been a mixed strategy of:
Hunting
Plant gathering
Scavenging
This would be efficient and evolutionarily stable.
First appears in Africa around 1.8 MYA.
Most likely evolved from H. habilis/rudolfensis.
May be the result of adaptive responses to harsh environmental conditions
Marks a major turning point in hominin evolution.
Brain sizes range from 727 cc-1251 cc, with a mean of 800 cc.
Endocasts suggest its brain was much more like a modern human’s than those of an earlier hominin or apes.
Feature pronounced supraorbital torii (brow ridges).
Some skulls features a sagittal keel.
Features considerable lower-face prognathism.
Smaller post-canine teeth and a more generalized dental pattern.
Larger body than previous hominins.
Much longer legs than arms.
Longer legs in ratio to body size.
Long, straight finger bones.
Greater bone density compared to modern humans (more robust).
Males averages 5’9'“ in height and weighed 145 lbs., whereas females averaged 5’3” and 112 lbs.
Moe sexual dimorphism in earlier members of the species than later ones.
Great anatomical variation amongst their populations.
Likely the first hominin to leave Africa.
Survived in large numbers until at least 300,000 years ago. Relic populations existed in Indonesia until as recently as 40,000-25,000 YA.
Most geographically successful hominin before the rise of modern Homo sapiens.
Possibly the first homin to use fire and cook food.
No unequivocal “hearth” (fire pit) has been found.
Deposits consistent with controlled fire have been discovered at a handful of sites.
Thousands of fossils have been found from many locations in Africa and Asia. Most of which have been skull fragments and teeth. Three partial skeletons have been found.
More H. erectus material than any earlier hominin.
Some early H. erectus individual in Africa seem to feature more primitive traits than later individuals and because of this, some scientists want to divide these hominins into two species:
Homo ergaster (Africa)
Homo erectus (Asia)
Others believe that H. ergaster is a regional variant of H. erectus. The regional variation has been argued to be no greater than that found amongst modern humans.
Nariokotome Boy
Found in 1984 in Lake Turkana, Kenya by Richard Leakey’s team.
A nearly complete skeleton of an adolescent male Homo erectus (Homo ergaster).
Age estimates are from 8-12 years. If he would have grown to full stature, he would have been around 6" feet tall.
His brain capacity was roughly 900 cc.
Homo erectus Dispersal
Seems to leave Africa by at least 1.8 MYA
Made it to western China by 1.6 MYA.
They appear in southern Indonesia (Java) by perhaps as early as 1.7 MYA.
Among the earliest finds outside of Africa are those in the Republic of Georgia, near the village of Dmanisi.
Dmanisi
Finds seem to represent a small colony of hominins.
Body and brain size of these individuals are very small by H. erectus standards. Some scientists see these as being transition figures between H. habilis and H. erectus. Others believe they should be classifies as H. habilis.
Region would have been quite old much of the years during this period. This implies these hominins had the cultural abilities to adapt to such conditions. Perhaps they had rudimentary clothes and/or dwellings. They may also have had the use of fire.
Only Olduwan-type tools have been found at this site.
Leaving Africa
As H. erectus are evolving, the African climate is both cooling and drying. Grasslands are expanding and forests contracting. These changes are stoking population increases in large grazing animals.
H. erectus is well-adapted for long distance travel.
Likely intelligent enough and had the technology to be at least part-time big-game hunters. There is evidence for meat growing in dietary importance. H. erectus may have been following food resources onto the vast Asian grasslands.
Lowered sea-levels meant there were more potential land routes from Africa to Asia than today.
Stone tools have been found in Europe dating to 1.2 MYA.
Oldest sites are Sima del Elefante (1.2 MYA) and Gran Dolina (900,000 YA.), both in Spain.
Some of these Spanish remains show evidence of cannibalism.
Many scientists argue these early European hominins carry modern traits.
For the first 300,000 years H. erectus’ existence, they used Olduwan tools. Between 1.7-1.5 MYA the Acheulean tool tradition begins in Africa and lasts until around 250,000 YA.
Used for butchering large animals, hunting tools, weapons used for the processing of plant foods.
Dominated by biface tools researchers call hand axes and cleavers.
NOT FOUND IN ASIA
Unlike Olduwan tools, Acheulean tools seem to be made for specifc uses.
Site found in England and dates to about 500,000 YA.
Likely created by H. antecessor.
Most complete example of archaic lifeways.
Seems to not have been a home base but a massive butchering area. It features the remains of many large and small game animals in association with many stone.
Animal bones show stone-tool cut marks underlying tooth marks of other animals.
Site features horse scapula that has a clear projectile wound.
A single tibia is the only hominin remain found at the site.
Earlier stone tools have been found in England dating 780,00 YA.
Found by American anthropologist Lee Berger in 2013 at Rising Star Cave, South Africa.
There are over 1,600 fossil remains representing at least 18 individuals of both sexes and various ages.
Shares many traits with early members of the genus homo.
Its cranial design has strong affinities with H. erectus (large brow ridges, a saggital keel, and reduced tooth size). However, post-cranially it features australopithecine-like traits.
Likely shares a common ancestor with H. erectus.
This find shows that relatively primitive hominins in Africa were living side-by-side with derived ones until quite recently.
No stone tools have yet been found attributable to this species.
The Flora and Fauna of Southeast Asia and Australia-New Guinea are radically different from each other.
Deep underwater trenches, produce powerful currents that keep most plants and animals from crossing them.
Ancient Island Tools
It was long believed that modern humans were the only hominins ever to reach islands south of the “Wallace Line.” However, in the 1990s, stone tools dating back to 900,000-700,000 YA were found on the island of Flores. More recently, stone tools of a similar age have been found on the nearby island of Sulawesi.
Found in the early 2000s by New Zealand archaeologist Mike Morwood’s team.
Discovered at Liam Bua Cave on Flores Island remains of extremely small hominins. They are roughly 3 feet tall and have brain sizes only in the high 300cc range.
Feature some traits associated with H. erectus.
Also have primitive australopithecine-like post-cranial traits.
Their teeth feature and unusual back-to-front compression to fit their small jaws.
The Liam Bua site also features primitive stone tools.
There is evidence there of butchered pygmy stegadons and the use of fire for cooking.
Recently at Mata Menge on Flores, remains of 700,000 YA hominins that strongly resemble those at Liam Bua have been found.
A small hominin species found recently at Callao Cave.
This island does not connect to the mainland during glacial periods.
So far only seven teeth, two hand bones, three foot bones, and one thigh bone have been found, thought to belong to two adults and one child.
Highly varied hominins began appearing between 500,000-350,000 YA. First in African then shortly after in Europe and Asia.
They feature traits associated with both H. erectus and later members of the genus Homo. They feature a great deal of anatomical and cultural diversity.
Some scientists have defined individual species (as many as 8) from these lineages, while other lump them under the single category Archaic Homo Sapiens.
Anatomical features include:
Larger brains (1,000cc-1,4000cc).
Taller, less angular cranial vaults.
Arching instead of straight supraorbital torii.
Same have wider nasal apertures.
Greater chin developments (in some groups).
Lower cranial vaults.
Larger, more robust faces.
More prognathic faces.
Thicker-walled, lower cranial vaults.
They used Levallois tools and techniques.
More specialized flake tools.
Stone was used much more efficiently
Smaller average brain size (in most cases).
More robust (thicker bones, more heavily muscled).
In some groups, there are significant dental issues.
Advantages
more energetically efficient than quadrupedal locomotion
frees hands for other uses
allows for improved long-distant vision
upright primates dissipate heat better than quadrupeds
Disadvantages
bipedal hominins are slower than their quadruped relatives
terrestrial living makes primates vulnerable to predation
early hominins would not seem to have had the size, intelligence, or cultural attributes to consistently offset this advantage
likely arose in a forest environment
early hominins likely would have needed to ascend trees at night to survive
believed it emerged as hominins shifted from fruit and leaf-based diets to one based around meat
saw the small canines of hominins as evidence that they were eating far fewer foods that need to be sliced and shredded
hominins adopted a hunting lifeway that created selective pressures for freeing up hands for creating tools
turned out to be wrong as data now shows that hominins only began regularly hunting and creating tools much later in their evolution
small brain sizes of the first hominins also show they likely lacked the cognitive abilities to be successful hunters
Stated that Africa was likely homeland to the first hominins
views were based on anatomical similarities between modern humans and African apes
reasoned that if our closest common living ancestors are Africa, so are our last common ancestors.
Patchy Forests
forests would have been reduced in size and density during dry periods
forest primates would have a selective advantage
Standing Feeding
arboreal mammals have difficulty feeding while gathering food in the trees so they often take their food to more stable branches or the ground
it has been hypothesized that bipeds in arboreal situations could be more comfortable eating in these areas
could have improved their energy allocation
Provisioning Hypothesis
proposed that bipedality may have emerges as part of an adaption where males provisioned females
males bringing them food improved energy allocation and allowed them to have more than one offspring at a time
implies monogamous relationships between males and females
also implies that there are selective advantages for males
these early hominin groups likely had social mechanisms that monitored behavior and promoted such male-female relationships
Canine Reduction
canine reduction is evidence of pair-bonded relationships
canines in all modern and fossil male apes are quite large and protruding and are used for fighting with or intimidating other males over sexual access to females
the earliest known hominin fossils show a marked reduction in canine size, compared to apes
Estrus Loss
modern female apes features an estrus cycle
refers when their genital region becomes swollen and discolored during ovulation
generally the only time when they are sexually receptive
modern humans have lost this estrus cycle
Lovejoy hypothesizes that this loss occurred at the beginning of hominin evolution to help promote pair-bonding
located in Africa
the result of faulting which has exposed millions of years of geologic strata
has featured regular volcanic activity for millions of years
allows for the application of Potassium-Argon dating methods
Sahelanthropus tchadensis
found in the northern desert of Chad
today this area is a grassland but data shows it was a swampy forest 7-6 MYA
holds some hominin features and some ape-like ones
was about the size of chimp and has a 350cc brain (small brain)
features a large supraorbital torus (brow ridge)
foramen magnum seemed to be positioned like that of a biped but could have been moved due to the skull being crushed and reformed
small canines and thick enamel on its molars
lack of shearing complex
flat face suggests it is not on the direct evolutionary lien to modern humans
Orrorin tugenensis
found near Lake Turkana, Kenya, in the Rift Valley
thick enamel on the molars
relatively large, ape-like canines
length and curvature of its femurs consistent with hominins
Ardipithecus ramidus
found in the Middle Awash river valley of Ethiopia (upper Rift Valley) by a team led by Timothy White
likely lived in a dense woodland but this area is now a desert
seems to have been both terrestrial and arboreal
45% of an individual skeleton has been found
about the size of a chimpanzee
brain in the low 400cc range
jutting lower face
grasping big toe (hallux)
foot has less-flexible muscularity typical of bipeds
hands and wrists are not anatomically designed for knuckle walking
does not feature evidence of brachiator anatomy
ape-like thin molar enamel
reduced canines
not much a shearing complex
lacking canine dimorphism between sexes
teeth feature thicker enamel than apes, but thinner than other hominins
Ardipithecus ramidus kadabba
found in the same region as the former and was likely its ancestor by a team led by Johannes Haile-Selassie
featured canine reduction but not to the same degree as A. ramidus
remains show a strong overall affinity with A. ramidus
Australopithecines
term coined by South African anatomist Raymond Dart
means “Southern Ape”
genus first discovered in the early 1920s in South Africa
numerous species have since been discovered in eastern and southern Africa though have never been found outside of Africa, like earlier hominins
all roughly within the size range of modern chimpanzees and bonobos
feature considerable sexual dimorphism
brain sizes range from the low to mid-400cc range
their feed do not have opposable big toes — closer to modern human feet than those of apes
still feature the following ape-like traits:
long, curved finger phalanges
shoulder joints still designed for suspensory locomotion
significant brow ridges
long arms
large teeth
ape-like hyoid bones
pyramid-shaped trapezoids
may have been regional creatures that spent time in the trees
exploited both forested and more open environments
practiced a mixed strategy likely of plant gathering, scavenging, and hunting of small game
likely made tools — most of which were made with materials, such as wood, that have not survived archaeologically
stone tools have been found dating back as far as 3.4 MYA+ which seem to have been used for digging and food processing as opposed to hunting
Australopithecus anamensis (4.0 MYA)
found in Kenya (Lake Turkana) by Maeve Leakey
Tim White believes it is a direct descendant of A. ramidus
has strong affinities with Au. afarensis
lived in a woodland environment
large molar with thick enamel
large canines and a slight shearing complex
ape-like u-shaped mandible
potentially featured canine dimorphism
sexual dimorphism in regard to body size
Australopithecus afarensis
discovered in 1974 by Don Johanson’s team at Hadar in Ethiopia
about the size of a chimp
avg. height for females is 3.5 and 4.9 feet for males
males potentially weighed twice as much as females
brain was in the 400cc range
features pronounced lower-face prognathism
lack opposable big toes and have very human-like feet
dental palate is less u-shaped compared to earlier hominins
large mandibles and teeth
thick enamel on molars
small canines and little canine dimorphism
except in regard to their size, teeth are more like later hominins than apes
first hominin species that lived in areas other than forests
seem to have occupied patchy woodlands, and open savannas
their teeth show a wide variety of wear patterns, indicating broad diets
large tooth and mandible size might have developed to eat hard foods found outside of forests
Australopithecus deyiremeda(3.5 - 3.3 MYA)
discovered by Yohannes Haile-Selassie in the Afar region of Ethiopia
strong affinities with Au. afarensis
very small teeth, which fall far outside the range of any other member of its genus
lived in woodlands and open areas
Australopithecus africanus ()
first reported by Raymond Dart in 1925
only found in southern African
potentially a direct descendant of Au afarensis
likely gave rise to other australopithecine species
may not be on the direct evolutionary line of humans
similar in size to A. afarensis
weighed between 65-95 lbs.
seems to be sexually dimorphic in regard to size
larger brains than earlier australopithecines (the mean being 454 cc)
less prognathic than A. afarensis
smaller, less specialized teeth than A. afarensis
“Taung Child” / Adult Au. africanus
Robust Australopithecines (2.5 - 1.3 MYA)
alternate genus = Paranthropus
found in southern and east Africa
arose from and have strong affinities with Au. africanus
roughly the same size as other australopithecines
brain size is in the 450cc range
extremely anatomically specialized
feature highly developed muscles of mastication
postorbital constriction, flares zygomatic arches; pronounces sagittal crests
chewing apparatus might be an adaption to harder, more fibrous foods
tooth-wear patterns in some individuals support this hypothesis
C4 analysis shows that at least one species (Au. boisei) specialized in eating grass
includes three difference species (that have been discovered)
Au. (P.) aethiopicus (2.6-2.5 MYA)
Au. (P.) boisei (2.3-1.2 MYA)
Au. (P.) robustus (2.0-1.5 MYA)
Au. aethiopicus and Au. boisei have only been found in eastern Africa whereas Au. robustus has only been found in southern Africa
Kenyanthropus platyops (“Flat face” — 3.5 MYA)
found by Maeve Leakey’s team in the region west of Lake Turkana (Kenya) in the late 1990s
seems to have lived in a woodland environment
small teeth and relatively flat face suggest that it is not an australopithecine
Australopithecus sediba (2.0-1.5 MYA)
found in the Malapa cave site in South Africa by American anthropologist Lee Berger in 2008
share features with both A. africanusand members of the genus Homo
features a 420cc-sized brain
tooth size similar to Homo, but design is more like A. africanus
pelvic shape similar to Homo, but foot structure similar to A. africanus
does not seem to be closely related to Au. robustus
Berger believes Au. sediba to be a link between the A. africanus and the genus Homo
others simply see parallel evolution at work and believe this species as another evolutionary dead end and their south African location relatively recent position in time would seem to go against their being a direct ancestor to our genus
Australopithecus garhi (“Surprise” — 2.5 MYA)
found in Ethiopia in 1999 by Ethiopian anthropologist Berhane Asfaw
upper limbs resemble those of A. afarensis, while lower limbs look like those of later hominins
leg and arm ratios are similar to later hominins
large premolars and molars (larger than the robust species)
large incisors
shares primitive facial and palate traits with Au. afarensis — large molars with thick enamel, relatively large canines, prognathic face, etc.
has 455cc brain size
primitive stone tools and animal bones with cut marks dating to the same period of Au. garhi have been in the region where this hominin lived
no other hominin find has been made in this region
early members of the genus homo made stone tools in this area
it’s geography, timing, and potential tool use make Au. garhi a strong candidate for a direct ancestor to the genus Homo
Climate
Ice sheets at the north and south poles (3 MYA - The Pliocene).
The Earth in general was cooling and drying at this time.
Glacial conditions become severe around 2.5 MYA.
The beginning of the Pleistocene (1.8 MYA) was a time of great climatic change. Yearly temperatures often fluctuated considerably, as did seasonal patterns.
Created unstable mosaic environments, which featured forests, patchy woodlands, savannas, and deserts.
Many species went extinct and new ones appeared — including primates/hominins.
Created strong selective pressures for intelligence and therefore increased socio-cultural abilities. The advantage would have gone to thsoe who could consistently live in multiple types of environments. Efficient longer-distance mobility may have been a key component.
Discovered in the early 1960s by Louis and Mary Leaky.
First found at Oldulvai Gorge in Tanzania, remains of a hominin dating to 2.5. MYA.
There are great differences in size within the members of this classification.
Certain very “robust” individuals have been found.
Some researchers believe these individuals are of a different species and have been classified as Homo rudolfensis. Others see this as an example of sexual dimorphism.
Remains are very fragmented and some researchers believe they are the remains of late-occurring members of a robust australopithecine species.
General Traits | Anatomical Changes (Compared to earlier hominins)
Males on average were 4.3 feet tall and females averaged 3.2 feet (similar to bonobos).
Males weight averaged 81 lbs. and females 70 lbs.
Brain sizes range form 503-661 cc, with a mean of 601 cc.
Still featured traits associated with autralopithecines (such as their general lower-body design).
Hand anatomy suggests that they had a more precise grips and greater manual dexterity.
Larger, more rounded brain-case.
Smaller, less jutting face.
Smaller post-canine teeth and large incisors.
Smaller chewing muscles
More efficient in their bidpedalism.
Seem to display greater intelligence.
Consist of flakes, cores, and hammer stones,
Flakes were used for slicing hides, butchering meat, and processing plant foods.
Cores are the stone from which flakes are “knocked off".”
Hammer stones were used to crack bone and to knock flakes off of cores.
Do not seem to be significantly specialized. They are used for roughly 2 MYA and change little throughout this period.
Some regional variation eventually develops within the industry. These tools will eventually be used by later hominin species.
H. habilis Lifeways — Hunters?
Meat becomes more important in hominin diets — evidence shots that early Homo butchered animals, often large ones.
Olduwan tools do not seem to be designed for hunting and appear to primarily be primitive processing tools.
Cognitive abilities and social structures also may not have been sufficient for them to live entirely by a hunting lifeway.
Behavioral ecology models show the most optimal lifeway would have been a mixed strategy of:
Hunting
Plant gathering
Scavenging
This would be efficient and evolutionarily stable.
First appears in Africa around 1.8 MYA.
Most likely evolved from H. habilis/rudolfensis.
May be the result of adaptive responses to harsh environmental conditions
Marks a major turning point in hominin evolution.
Brain sizes range from 727 cc-1251 cc, with a mean of 800 cc.
Endocasts suggest its brain was much more like a modern human’s than those of an earlier hominin or apes.
Feature pronounced supraorbital torii (brow ridges).
Some skulls features a sagittal keel.
Features considerable lower-face prognathism.
Smaller post-canine teeth and a more generalized dental pattern.
Larger body than previous hominins.
Much longer legs than arms.
Longer legs in ratio to body size.
Long, straight finger bones.
Greater bone density compared to modern humans (more robust).
Males averages 5’9'“ in height and weighed 145 lbs., whereas females averaged 5’3” and 112 lbs.
Moe sexual dimorphism in earlier members of the species than later ones.
Great anatomical variation amongst their populations.
Likely the first hominin to leave Africa.
Survived in large numbers until at least 300,000 years ago. Relic populations existed in Indonesia until as recently as 40,000-25,000 YA.
Most geographically successful hominin before the rise of modern Homo sapiens.
Possibly the first homin to use fire and cook food.
No unequivocal “hearth” (fire pit) has been found.
Deposits consistent with controlled fire have been discovered at a handful of sites.
Thousands of fossils have been found from many locations in Africa and Asia. Most of which have been skull fragments and teeth. Three partial skeletons have been found.
More H. erectus material than any earlier hominin.
Some early H. erectus individual in Africa seem to feature more primitive traits than later individuals and because of this, some scientists want to divide these hominins into two species:
Homo ergaster (Africa)
Homo erectus (Asia)
Others believe that H. ergaster is a regional variant of H. erectus. The regional variation has been argued to be no greater than that found amongst modern humans.
Nariokotome Boy
Found in 1984 in Lake Turkana, Kenya by Richard Leakey’s team.
A nearly complete skeleton of an adolescent male Homo erectus (Homo ergaster).
Age estimates are from 8-12 years. If he would have grown to full stature, he would have been around 6" feet tall.
His brain capacity was roughly 900 cc.
Homo erectus Dispersal
Seems to leave Africa by at least 1.8 MYA
Made it to western China by 1.6 MYA.
They appear in southern Indonesia (Java) by perhaps as early as 1.7 MYA.
Among the earliest finds outside of Africa are those in the Republic of Georgia, near the village of Dmanisi.
Dmanisi
Finds seem to represent a small colony of hominins.
Body and brain size of these individuals are very small by H. erectus standards. Some scientists see these as being transition figures between H. habilis and H. erectus. Others believe they should be classifies as H. habilis.
Region would have been quite old much of the years during this period. This implies these hominins had the cultural abilities to adapt to such conditions. Perhaps they had rudimentary clothes and/or dwellings. They may also have had the use of fire.
Only Olduwan-type tools have been found at this site.
Leaving Africa
As H. erectus are evolving, the African climate is both cooling and drying. Grasslands are expanding and forests contracting. These changes are stoking population increases in large grazing animals.
H. erectus is well-adapted for long distance travel.
Likely intelligent enough and had the technology to be at least part-time big-game hunters. There is evidence for meat growing in dietary importance. H. erectus may have been following food resources onto the vast Asian grasslands.
Lowered sea-levels meant there were more potential land routes from Africa to Asia than today.
Stone tools have been found in Europe dating to 1.2 MYA.
Oldest sites are Sima del Elefante (1.2 MYA) and Gran Dolina (900,000 YA.), both in Spain.
Some of these Spanish remains show evidence of cannibalism.
Many scientists argue these early European hominins carry modern traits.
For the first 300,000 years H. erectus’ existence, they used Olduwan tools. Between 1.7-1.5 MYA the Acheulean tool tradition begins in Africa and lasts until around 250,000 YA.
Used for butchering large animals, hunting tools, weapons used for the processing of plant foods.
Dominated by biface tools researchers call hand axes and cleavers.
NOT FOUND IN ASIA
Unlike Olduwan tools, Acheulean tools seem to be made for specifc uses.
Site found in England and dates to about 500,000 YA.
Likely created by H. antecessor.
Most complete example of archaic lifeways.
Seems to not have been a home base but a massive butchering area. It features the remains of many large and small game animals in association with many stone.
Animal bones show stone-tool cut marks underlying tooth marks of other animals.
Site features horse scapula that has a clear projectile wound.
A single tibia is the only hominin remain found at the site.
Earlier stone tools have been found in England dating 780,00 YA.
Found by American anthropologist Lee Berger in 2013 at Rising Star Cave, South Africa.
There are over 1,600 fossil remains representing at least 18 individuals of both sexes and various ages.
Shares many traits with early members of the genus homo.
Its cranial design has strong affinities with H. erectus (large brow ridges, a saggital keel, and reduced tooth size). However, post-cranially it features australopithecine-like traits.
Likely shares a common ancestor with H. erectus.
This find shows that relatively primitive hominins in Africa were living side-by-side with derived ones until quite recently.
No stone tools have yet been found attributable to this species.
The Flora and Fauna of Southeast Asia and Australia-New Guinea are radically different from each other.
Deep underwater trenches, produce powerful currents that keep most plants and animals from crossing them.
Ancient Island Tools
It was long believed that modern humans were the only hominins ever to reach islands south of the “Wallace Line.” However, in the 1990s, stone tools dating back to 900,000-700,000 YA were found on the island of Flores. More recently, stone tools of a similar age have been found on the nearby island of Sulawesi.
Found in the early 2000s by New Zealand archaeologist Mike Morwood’s team.
Discovered at Liam Bua Cave on Flores Island remains of extremely small hominins. They are roughly 3 feet tall and have brain sizes only in the high 300cc range.
Feature some traits associated with H. erectus.
Also have primitive australopithecine-like post-cranial traits.
Their teeth feature and unusual back-to-front compression to fit their small jaws.
The Liam Bua site also features primitive stone tools.
There is evidence there of butchered pygmy stegadons and the use of fire for cooking.
Recently at Mata Menge on Flores, remains of 700,000 YA hominins that strongly resemble those at Liam Bua have been found.
A small hominin species found recently at Callao Cave.
This island does not connect to the mainland during glacial periods.
So far only seven teeth, two hand bones, three foot bones, and one thigh bone have been found, thought to belong to two adults and one child.
Highly varied hominins began appearing between 500,000-350,000 YA. First in African then shortly after in Europe and Asia.
They feature traits associated with both H. erectus and later members of the genus Homo. They feature a great deal of anatomical and cultural diversity.
Some scientists have defined individual species (as many as 8) from these lineages, while other lump them under the single category Archaic Homo Sapiens.
Anatomical features include:
Larger brains (1,000cc-1,4000cc).
Taller, less angular cranial vaults.
Arching instead of straight supraorbital torii.
Same have wider nasal apertures.
Greater chin developments (in some groups).
Lower cranial vaults.
Larger, more robust faces.
More prognathic faces.
Thicker-walled, lower cranial vaults.
They used Levallois tools and techniques.
More specialized flake tools.
Stone was used much more efficiently
Smaller average brain size (in most cases).
More robust (thicker bones, more heavily muscled).
In some groups, there are significant dental issues.