The Dawn of Man Fossil Hominids The Critters Australopithecines Sahelanthropus tchadensis A. robustus A. boisei • Unveiled July 10, 2002 • Toros-Menalla locality, Djurab Desert, northern Chad, central Africa • Fauna includes aquatic and amphibious animals alongside gallery forest and savanna fauna A. garhi A. aethiopicus A. africanus A. bahrelghazali K. platyops A. afarensis A. anamensis Ardipithecus – Fish, crocodiles, primates, rodents, elephants, equids, bovids Ar. ram. kadabba O. tugenensis S. tchadensis 7 6 5 4 3 2 Millions of Years Ago 1 • Suggests hominid lived close to a lake, but not far from a sandy desert • Biochronology suggests an age between 6 and 7 million years Sahelanthropus tchadensis Sahelanthropus tchadensis • Six specimens: nearly complete skull and several fragmentary lower jaws • Unique mosaic of primitive and derived characters – Primitive: small cranial capacity (320-380 cc), large central incisor, non-incisiform canines – Derived: Reduced canines, thick molar enamel, nuchal crest positioning suggesting bipedalism • Skull nicknamed Toumaï – Local name for a child born perilously close to the start of the dry season (fossils occurred near the earliest evidence of a central African desert) 1 Orrorin tugenensis • Lukeino Formation at Tugen Hills, Kenya • Dated at 6 m.y.a. • Discoverers take great pains to show disimilarity between Ororrin and the australopithecines, and similarity between Orrorin and Homo – The teeth are relatively small and retain thick enamel – Femur does not rule out bipedalism, but is inconclusive Orrorin tugenensis Earliest Hominids LT 329: Lothagam Photo by I.M. Campbell • Dating is set at 5.8 – 5.6 mya • Jaw fragment shows numerous features reflecting improved power and efficiency in molar grinding – Cannot be distinguished from later Pliocene australopithecines including A. afarensis (Kramer) and A. ramidus (White) Ardipithecus ramidus kadabba Toe Toebone bone Ardipithecus ramidus kadabba • • • • Discovered at Aramis, Ethiopia Announced in July 2001 Dated at 5.2 – 5.8 million years Several jaw and bone fragments – Toe bone resembles A. afarensis, suggesting bipedality Mandible fragment 2 Ardipithecus ramidus Ardipithecus ramidus ramidus • • • • • Discovered at Aramis, Ethiopia Announced in September 1994 Dated at 4.4 million years Remains consist of skull and jaw fragments. Other fossils found with it indicate that it may have been a forest dweller Ardipithecus ramidus--2 • Teeth are intermediate between those of earlier apes and A. afarensis, but one baby tooth is very primitive, resembling a chimpanzee – Thin enamel on the molars • Undescribed remains suggest bipedalism – Foramen magnum positioned forward – Humerus does not appear to be weight bearing – Limestone encased partial skeleton suggests bipedality New Controversy • For over a century we have expected fossils to look more and more ape-like as we approach the common ancestor with chimps • Recently a number of the features that have been assumed to be derived associated with the face and teeth are being re-evaluated – We’re beginning to think that the common ancestor looked more hominid than ape-like in these features, making it more difficult to tell when we have a very early hominid like Sahelanthropus or Orrorin Original Model Modern African Apes Modern Man 6 - 8 million years New Notions Modern African Apes 6 - 8 million years Common Ancestor Common Ancestor More ape-like Modern Man More hominid-like More ape-like More hominid-like 3 Australopithecus anamensis Australopithecus anamensis • Named in August 1995 • Material consists of 9 fossils from Kanapoi in Kenya and 12 fossils from Allia Bay in Kenya • Aged between 4.2 and 3.9 million years ago • Mixture of primitive features in the skull, and advanced features in the body Australopithecus anamensis--2 • Teeth are a mix of features – Hominid thick enamel on molars – Ape-like sectorial lower first premolar – Relatively large canines • Tibia suggests bipedality • Humerus is extremely hominid in form Australopithecus afarensis Lucy: 40% complete skeleton Sectorial premolars Australopithecus afarensis • Aged between 3.9 and 3.0 million years ago • Apelike face with a low forehead, a bony ridge over the eyes, a flat nose, and no chin • Cranial capacity from 375 to 500 cc – Within chimp range, 1/4 - 1/3 modern humans • Pelvis and leg bones far more closely resemble those of modern man, and leave no doubt that they were bipedal Australopithecus afarensis Guesstimate based on fragments First nearly complete skull 4 Australopithecus afarensis, 4 • Laetoli footprints • Discovered by Mary Leakey • Volcanic tuff dated at almost 3.5 million years • Upright, bipedal locomotion of two or three hominids Australopithecus afarensis, 5 • Canine teeth are much smaller than those of modern apes, but larger and more pointed than those of humans, and shape of the jaw is between the rectangular shape of apes and the parabolic shape of humans • Females were substantially smaller than males, a condition known as sexual dimorphism Australopithecus bahrelghazali Australopithecus afarensis, 6 • Height varied between about 107 cm (3'6") and 152 cm (5'0") • Finger and toe bones are curved and proportionally longer than in humans, but the hands are similar to humans in most other details Australopithecus bahrelghazali • Age estimated at 3 - 3.5 mya due to faunal similarity with Hadar • Single mandibular fragment is generally similar to Australopithecus afarensis – Incisiform canines, bicuspid first premolar • Differences from A. afarensis include: – More verticle interior surface of the mandibular symphysis – Premolars have thin enamel and three roots (afarensis usually has one or two roots) Kenyapithecus platyops • From the site of Lomekwi, western side of Lake Turkana in northern Kenya, named in 2001 • More than 30 skull and dental fragments – Two have been assigned to K. platyops – Other fragments not yet assigned to any genus or species Photograph by Michel Brunet KT12/H1 • Found in deposits reliably dated to between 3.5 million and 3.2 million years ago • Other mammalian species found at Lomekwi suggest that the site was part of a complex mixture of grassland and wooded habitats – Like other roughly contemporary sites such as Laetoli (Tanzania) and Hadar (Ethiopia), where remains of A. afarensis have been found 5 Kenyapithecus platyops Lieberman on Kenyapithecus platyops • The fossil resembles chimpanzees and A. anamensis in having a small earhole – It shares many other features of primitive hominins with A. afarensis and A. anamensis • Cheek teeth with thick enamel • A small brain the size of that of a chimpanzee • Flat nasal margins • It also has several important derived features – An anterior origin for the root of the cheekbone arch on the upper jaw – The existence of a flat plane beneath the nose bone (and so the appearance of a flat face) – A tall cheek region Holotype KNM-WT 40000 a, left lateral view (markers indicate the plane separating the distorted neurocranium and the well-preserved face). b, Superior view. c, Anterior view. d, Occlusal view of palate. Paratype KNM-WT 38350. e, Lateral view. KNM-WT 40001. f, Lateral view. g, Inferior view. Scale bars: a–c, 3 cm; d–g, 1 cm. (Leakey et al. 2001) • Postcanine teeth and brow of the skull are smaller than in A. garhi Kenyapithecus platyops More Lieberman vs. Homo rudolfensis • KNM-WT 40000 has a small cranial capacity but otherwise looks much like the famous KNM-ER 1470 fossil, generally referred to as Homo rudolfensis – These similarities are mostly in the face, and include the flat plane beneath the nose bone, the tall, vertically oriented cheek region, and the lack of a depression behind the ridge of the brow. KNM- WT 40000 Taung Child KNM- ER 1470 Mrs. (?) Ples (Sts 5) Australopithecus africanus • A. africanus existed between 3 and 2 million years ago • Similar to afarensis, bipedal, but slightly larger body • Cranial capacity ranging between 420 and 500 cc • Molars are a little bigger than in afarensis 6 Australopithecus africanus, 2 • The shape of the jaw is fully parabolic, like humans • The canine teeth, diastema in upper dentition, and sectorial first lower premolars are further reduced compared to A. afarensis Australopithecus garhi Photograph by David Brill Australopithecus garhi • From Bouri, Middle Awash, Ethiopia, 2.5 m.y.a. • Large teeth – Cheek teeth at or beyond the robust australopithecine extremes – Large anterior teeth • Bigger than those of the largest australopithecines • Based on tooth size A. garhi fits with schemes that see gracile australopithecines as a direct human descendents – Canine-to-premolar/molar size ratios are comparable between A. garhi, the gracile australopithecines and early Homo • Long forelimbs and long hindlimbs • Researchers argue that A. garhi represents a direct ancestor of modern humans that is derived from africanus which is likely derived itself from afarensis Australopithecus aethiopicus • Lived between 2.6 and 2.3 million years ago – Known from one major specimen, the Black Skull, and a lower jaw from Omo – May be an ancestor of robustus and boisei, but it has a baffling mixture of primitive and advanced traits • Brain size is small, at 410 cc Australopithecus aethiopicus Australopithecus aethiopicus Photograph by David Brill Photograph by Robert I.M. Campbell Photograph by Robert I.M. Campbell 7 Australopithecus aethiopicus Australopithecus aethiopicus • Parts of the skull, particularly the hind portions, are very primitive, most resembling A. afarensis • The massive face, jaws, and single tooth found, and the largest sagittal crest (the bony ridge on top of the skull to which chewing muscles attach) in any known hominid, are more reminiscent of A. boisei Photograph by Robert I.M. Campbell Australopithecus robustus Australopithecus robustus • Body similar to A. africanus, but larger and more robust skull, jaws, and teeth • Found primarily in cave deposits estimated at 1½ - 2 mya from Swartkrans and Kromdraai in South Africa • Massive face is flat or dished, with no forehead and large brow ridges • Relatively small front teeth, but massive grinding teeth (molars and premolars) in a large lower jaw Australopithecus robustus, 3 • Most specimens have sagittal crests • Diet would have been mostly coarse, tough food that needed a lot of chewing • Average brain size is about 530 cc • Animala bones excavated with A. robustus skeletons suggest to some workers that the australopithecines may have used bones as digging tools Australopithecus boisei • A. boisei existed between 2.1 and 1.1 million years ago • Similar to A. robustus, but the face and cheek teeth even more massive • Cranial capacity averages about 530 cc • Some experts consider A. boisei and A. robustus to be variants of the same species – Others place them in a separate genus, Paranthropus 8 KNM-ER 406 Gracile vs. Robust • Australopithecus afarensis and A. africanus are known as gracile australopithecines, because of their relatively lighter build, especially in the face and teeth – Gracile means slender, and in paleontology is used as an antonym to robust – Despite this, A. afarensis and A. africanus were still more dentally robust than modern humans Photograph by David Brill Gracile vs. Robust, 2 • Australopithecus aethiopicus, A. robustus and A. boisei are known as robust australopithecines, because their skulls are more heavily built Discovery of this jaw in 1960 led Louis Leakey to name a new species, Homo habilis, as direct ancestor of man, with Homo erectus representing an extinct side branch OH 7 – The jaws, cheek teeth, and face are the most heavily built aspects of these fossil hominids – The canine teeth are quite small in all of these species Photograph by John Reader Homo habilis • Fossils named “handy man” because of the suggestion of evidence of tools found in contemporary deposits • Lived between about 2.4 and 1.5 million years ago • Similar to australopithecines in many ways • Face is primitive, but projects less than in A. africanus Photograph by John Reader KNM-ER 1813 Photograph by David Brill 9 Homo habilis, 2 • Back teeth are smaller than those of the australopithecines, but still considerably larger than modern humans • Average cranial capacity, at 650 cc, is larger than in australopithecines – Brain size varies between 500 and 800 cc, overlapping the australopithecines at the low end and H. erectus at the high end Homo habilis, 4 Homo habilis, 3 • Brain shape is more humanlike – Bulge of Broca's area, essential for speech, is visible in one H. habilis brain cast, indicating it may have been capable of rudimentary speech • H. habilis was about 127 cm (5'0") tall, and about 45 kg (100 lb) in weight, although females may have been smaller KNM-ER 1470 Homo rudolfensis • Habilis has been a controversial species – Some scientists have not accepted it, believing that all H. habilis specimens should be assigned to either the australopithecines or Homo erectus – Many now believe that Homo habilis combines specimens from two or three different species • Homo habilis • Homo rudolfensis • Homo ergaster Photographs by David Brill Homo rudolfensis • The species designation of Homo rudolfensis is much debated KNM-ER 992 Homo ergaster – Is it a separate species – Is it an australopithecine rather than a homonine • One of the main problems with H. rudolfensis species is that there are no postcranial remains – Large brains in conjunction with megadont postcanines – Some researchers see the larger brain and tooth size as indicative of allometric changes due to increased body size--rudolfensis and habilis are the same, with the former the males and the later the females – Some see rudolfensis as the ancestor of habilis with a decrease in brain size occurring – Others see the two on completely different evolutionary lines Photograph by Robert I.M. Campbell 10 Homo ergaster KNM-WT 15000 • Homo ergaster is one of the more problematic of species designations • Each researcher that sees ergaster as valid sees different specimens as belonging or not belonging • Most researchers see too little difference between ergaster and erectus to form the basis of a species • As a general rule of thumb, one can consider most attributed ergaster specimens to be early erectus geographically confined to Africa Photographs by David Brill Homo erectus from Zhoukoudian Weidenreich Tattersall and Sawyer Homo erectus • Wolpoff claims that H. erectus is an invalid taxon, though few accept this interpretation at this point in time • Others believe the material attributed to erectus should be split into several different taxons – Asian and later African material remaining as H. erectus--not contributing to modern humans – Early African material as H. ergaster – European material as H. heidelbergensis Photographs by David Brill KNM-ER 3733 Homo erectus • An increase in brain size to approximately 900 cc • Reduction in postcanine dentition and a decrease in jaw size • Vertical shortening of the face. • Shortening arm bones, especially forearms to very modern limb proportions – Postcranial proportions are very similar to tropically adapted modern humans Photographs by David Brill • Development of a more barrel-shaped chest • The formation of an external nose • Modern human size in terms of height 11 Homo antecessor • Approximate brain size of 1000 cc • Marked double-arched browridge Gran Dolina Material Homo antecessor – like later Neanderthals and Chinese H. erectus • Canine fossa but no expanded maxilla – May be due to the individual's young age since others (ATD 658) have an expanded maxilla • Sharp nasal margin • Shallow maxillary notch • Reduced mandibular corpus thickness when compared to H. ergaster or early H. erectus • Small postcanines that resemble those of the habilines • M3 reduced relative to M1 • Moderate taurodontism – Characteristic of H. erectus and H. heidelbergensis) • Large I2 dimensions that resemble H. heidelbergensis Homo antecessor Photograph by Javier Trueba Homo heidelbergensis from Arago • An important feature that was discovered when the remains were examined were cut marks that were present on most of the material – 12 parallel cut marks on a temporal fragment where the sternocleidomastoid muscle attaches – Cut marks on two foot phalanges where the flexor muscle lies • Dismemberment was the likely goal • Faunal material shows the same cut marks as the hominid remains – Very few carnivore tooth marks indicates that hominids were mainly responsible for processing the bones • This is the earliest well-documented case of cannibalism in a hominid population, and this information is important for deciphering the behavior of early hominids Photographs by David Brill Homo heidlebergensis • An increase in brain size to approximately 1200cc • A shift in the widest part of the brain case from the cranial base to the parietal regions • The rear of the cranial vault becomes more vertical • A gradual reduction in cranial robusticity • A decline in postcranial robusticity • A tendency for a shift from shorter more robust stature to taller, leaner bodies Mauer 1 Homo heidlebergensis • 1907 Mauer sand pits in Germany • Validated Schoetensack's conviction that Pleistocene human remains would be found in the quarry – Associated with rhino, bear, elephant, bison, deer, and horse • Schoetensack (1908) named a new species of hominid, Homo heidelbergensis – New species not justified by describing unique anatomical features of the species – Lack of older or other specimens kept heidelbergensis from being accepted Photograph by John Reader 12 Homo heidelbergensis Homo neanderthalensis Neanderthal 1 Photograph by Rheinisches Landesmuseum Bonn Homo neanderthalensis Homo neanderthalensis Mount Circeo La Chapelle-aux-Saints Photographs by John Reader Photograph by Ministry of Culture, Italy Inner Ear Morphology Homo neanderthalensis • An occipital bun • A suprainiac fossa • Position of the mastoid crest located behind the external auditory meatus • Position of the juxtamastoid crest located behind the mastoid crest, and often larger than the mastoid process • Position of the mastoid process • The supraorbital torus • The supratoral sulcus • A receding frontal • Presence of lambdoidal flattening Drawings by C. David Kreger • • • Another trait that is being looked at currently as a way of distinguishing Neanderthals in the inner ear morphology Researchers are trying to determine if the Neanderthals had a unique inner ear morphology that can be used When comparing the values of S/I, humans generally have a value close to 1, chimpanzees have values greater than 1, and Neanderthals have values less than 1 13 References • LEAKEY, MEAVE G., FRED SPOOR, FRANK H. BROWN, PATRICK N. GATHOGO, CHRISTOPHER KIARIE, LOUISE N. LEAKEY & IAN MCDOUGALL (2001) New hominin genus from eastern Africa shows diverse middle Pliocene lineages. Nature 410, 433 – 440. • LIEBERMAN, DANIEL E. (2001) Another face in our family tree Nature 410, 419 – 420. • Kreger, C. David (2001) A look at modern human origins. http://www.modernhumanorigins.com/ Possible evolutionary relationships of the hominids • The five major genera, with Kenyanthropus in red, Homo in blue, Paranthropus in green, Australopithecus in black and Ardipithecus in yellow – Question marks indicate hypothetical or conjectural relationships; horizontal bars indicate uncertainty in the species' temporal spans • Lieberman, 2001 14