Part III: Later Hominin Evolution, Part I

Chapter 14: The Origin of Modern Humans: Background and Fossil Evidence

This chapter deals with the evolutionary transition from Homo erectus to Homo sapiens and the scientific arguments to how this transition has occurred. Anthropologists agree on certain anatomical and behavior changes in this transition, namely a decrease in skeletal and dental robusticity, modifications in locomotor functional anatomy, and an increase in cranial volume for anatomy; and the increase in diverse tool technologies, more efficient foraging strategies, more complex social organizations, full development of spoken language, and artistic expression for behavior.

The two extreme viewpoints within paleoanthropology of the transition that took place is that on one side a gradual change within all populations of Homo erectus took place simultaneously, leading to the appearance of Homo sapiens in Africa and Eurasia. On the other side, modern humans have a single African origin that spread out across the old world and replaced non-modern populations. These extreme viewpoints are supported by different anatomical, genetic, and archaeological evidence with the weight of the evidence currently supporting a form of the single-origin model. Chapter 14 covers the anatomical evidence.

Two scenarios exist for the evolution of Homo in explaining how Homo sapiens came into being. In, the “Homo erectus as general ancestor” scenario, Homo as a new grade of hominin was established in Africa about 2 million years ago, and eventually spread itself across the old world. Having this large and widespread population, considerable local variation can be expected that could largely be minor, but certain major adaptations could be transmitted – either thru gene flow or cultural transmission – to homogenize the larger population. Speciation does not occur because of the large amount of minor variations taking place, but the overall homogenous effects for the whole population would serve as the evolutionary change. In this model, major behavioral differences would not be developed due to the homogenization across the larger population through genetic flow and cultural transmission.

The second scenario, “Homo as separate local trajectories” posits that H. ergaster dispersed out of Africa at a later point into relatively small, isolated populations. These populations would be prone to greater differentiation through drift or selection, but also more prone to extinction. This would cause each population to be more prone to form species boundaries and for local evolutionary trajectories to be independently established – recognizing H. erectus and H. ergaster as the result of evolutionary divergence. H. sapiens, then, would evolove from one of these trajectories. In this model, behavioral difference would become very distinct due to local isolation, leading to several modes of hominin behavior being present at all times – the long-term effects of this being a major component of later human evolution.

Competing Hypotheses for Modern Human Origins

The multiregional hypothesis originated in the 1940s from German anatomist Franz Weidenreich. He believed that anatomical diversity evolved from distinctive traits in different geographical regions from the time of H. erectus through modern humans, which he referred to as regional continuity. Recently, Alan Thorne and Milford Wolpoff have built on the multiregional hypothesis to what is now known as multiregional evolution hypothesis, which sees the transformation of H. erectus to H. sapiens as a “balance between the maintenance of distinctive regional traits in anatomy, through local regional adaptation, and the maintenance of a genetically coherent network of populations throughout the Old World, through significant gene flow” (p. 372). For this to be true, three expectations should hold true: anatomically modern humans will appear in the Old World during a similar period, transitional fossils (archaic-modern) should be found in all of the Old world, and in each Old World region, continuity should be apparent for the anatomy of ancient to modern populations.

The single-origin hypothesis dates to the 1960s from Louis Leakey, who believed that Middle Pleistocene hominins from Africa are better models than the H. erectus fossils of Asia, which he believed to be evolutionary dead-ends. Chris Stringer builds on the single-origin model of the replacement of archaic populations by invading modern populations by believing that today’s regional anatomical traits are the result of adaptation and genetic drift locally in the past 100,000 years. For this to be true, four predictions should hold: anatomically modern humans should be found in Africa much earlier than other areas, transitional fossils from archaic-modern should only be found in Africa, traits distinguishing modern geographical populations should show no links to early populations in the same region, and there should be little to no evidence showing hybridization between archaic and early anatomically modern populations.

Chronological Evidence

Specimens of anatomically modern humans from Africa and the Middle East date to be significantly older than those found in the rest of the Old World. The oldest recorded modern human population comes from the Middle Awash region of Ethiopia dating to 130,000 years ago, found by Tim White in 2003, naming the subspecies Homo sapiens idaltu. In the Middle East, Israeli cave sites have yielded specimens dating close to 100,000 years ago although retaining some archaic features. Nevertheless, scientists claim the specimens to be essentially modern. Asian sites have yielded older anatomically modern specimens, but their origin dates are widely argued and rejected, leading most scientists to believe the specimens to be only 60,000 years old. There is therefore a chronological gap that exists of tens of thousands of years between specimens found in the African/Middle Eastern region and those found in the rest of the old world, therefore giving claim to the ‘out of Africa’ hypothesis.

The Question of Regional Continuity

Because the multiregional hypothesis depends on regional continuity, scientists must find proof of such continuity in the fossil record – a contentious subject, to say the least. Figure 14.5 (p. 376) nicely lays out the chronology of anatomically modern humans region by region, which strongly supports the ‘out of Africa’ hypothesis.

- As the authors lay out each argument of each fossil find (pp. 377-391), does this support the argument that scientists are basing their observations of fossil finds

on a priori premises? Does this apply to the lumping vs. splitting debate as well?

The authors state the importance of voices outside of the current debate in interpreting which hypothesis is correct. Both Aiello and F. Clark Howell are cited as siding more with the out of Africa theory, but that no hypothesis yet can completely explain the observed fossil evidence. Further, Marta Lahr’s study of cranial features concludes that no substantial morphological evidence exists to support the multiregional model, as well as Diane Waddle’s matrix correlation tests.

The Place of Neanderthals in Human Evolution

The authors discuss the importance of Neanderthal findings because of the early discovery in the Neander valley in 1856 (three years before the publication of Origin) and the substantiation they gave to the debate of modern humans as evolved animals. Although the argument of Neanderthals being the ‘missing link’ has long been abandoned because of the subsequent findings of older hominin forms, the Neanderthals remain important in the history of paleoanthropology as a ‘test-bed for many ideas about the human evolutionary past’ (p. 395). One such important argument was put forth by Lewis Binford’s analysis that Neanderthals were behaviorally very different from modern humans, and that the contrast between the Middle and Upper Paleolithic shows the change from non-human to human behavior, or the “cultural revolution”. The current view holds that modern humans and Neanderthals diverged at some point within the last half million years and recorded parallel evolutionary histories – making the two groups two separate species, Homo sapiens and Homo neaderthalensis. The genetic evidence of chapter 15 substantiates this theory.

-Does the historical importance placed on studying Neanderthals help show the extent of western-centric bias in the sciences?

Chapter 15: The Origin of Modern Humans: Genetic Evidence

The Impact of Molecular Evolutionary Genetics

Genetic evidence has begun to show just how complex the event of the origin of modern humans really was, and in turn how simple the hypotheses based on fossil evidence really are. Douglas Wallace first studied this in the 1980s by focusing on mitochondrial DNA, inspiring the famous ‘mitochondrial eve’ hypothesis. This posits that all mitochondrial DNA of living humans can be traced back to a single female living in Africa approximately 200,000 years ago. This female would have been in a population of about 10,000 individuals, all relating to the foundation of the modern human population who spread across the old world and replaced all existing archaic species of Homo. This data was deemed inadequate during the 1990s (see p. 405 for a detailed analysis), with genetic work shifting to two pathways: one extending mitochondrial DNA analysis to include other genes (including ones from the nucleus) to determine when and where humans evolved, and the other using mitochondrial DNA to infer population dynamics of early modern humans – both supporting the single-origin ‘out of Africa’ claim.

Mitochondrial DNA is useful for understanding recent evolutionary events for two reasons: first, because it accumulates mutations ten times faster than in nuclear DNA therefore providing more information over the short term; and second, because it is inherited only from the mother, it substantially cuts through the fog that recombination (maternal and paternal) genes create. The evidence collected from mitochondrial DNA supports a recent bottlenecked, single-origin model of the human lineage.

The problem with studying mitochondrial DNA is that it provides a gene history, not a population history. The mitochondrial is just one special gene and scientists now realize the need to study other genes to search for evidence to substantiate evolutionary claims.

Recent Developments

Scientists are now looking at two new types of genetic data, the first being microsatellites which are rapidly evolving short stretches of DNA of two-to-five-nucleotide segments. David Goldstein has used this technique to find a coalescence point of origin of approximately 156,000 years ago. The second is Alu elements, which are sequences of DNA approximately 300 base pairs long that are inserted in large numbers over the nuclear genome. Once these are inserted, they are never removed and therefore remain immune to homoplastic changes. A recent multi-authored analysis has resulted in a coalescence time of 102,000 years.

Another study focuses on the fact that because mitochondrial DNA helps give the history of women, the Y sex chromosome will help give the history of men, because only men possess it. Stanford University scientists are using the Y chromosome to obtain a coalescence of between 100,000 and 150,000 years, with a pattern showing greater African diversity than the rest of the world’s modern populations.

The importance of coalescence times in different genetic studies shows how some genetic systems have older patterns of diversity, even if there was a ‘harsh population bottleneck’ of 150,000 years ago that is supported by this evidence. Therefore, studying the complexity of different genes and their coalescence times will help broaden our understanding of our overall population history.

This has led to the study of the bottlenecking of modern human populations over history, with the severe reduction coming from different environmental events followed by the explosion in numbers of individuals in the population. Certain hypotheses have been put forth supported by genetic evidence, including the Garden of Eden hypothesis (figure 15.14, p. 415), which posits that humans fragmented within Africa forming distinct genetic populations. Subsequent population bottlenecks within Africa led to ‘proto-‘ European, African, and Asian populations that then began to spread across the old world. The authors deem this argument to be very weak, but nevertheless one of the many hypotheses developed in the out of Africa model. Figure 15.16 (p. 419) further illustrates the evidence of the history of bottlenecking in human evolution and the relation between genetics and population dynamics – all supporting the out of Africa hypothesis.

-As the field of molecular genetics expands in trying to explain the origin of modern humans, what can be learned from the past in forming sound hypotheses?

Chapter 16: The Origin of Modern Humans: Archeology, Behavior, and Evolutionary Process

This chapter explores the archaeological evidence that would help support the claim that modern human behavior would start first in Africa and spread out to the rest of the old world. This archaeological evidence should substantiate the link between behavior and biology in the history of modern human populations and whether biology led to behavior or vice versa. However, a gap exists in these findings because the small amount of sites in Africa (only about a dozen) in comparison with other sites (SW France, for example with 100 sites, but 100 times smaller than the area in East Africa). This can lead to misinterpretations (Eurocentric, specifically) because of the lack of evidence in the archaeological record, so much work needs to be done to further the out of Africa hypothesis from the archaeological and behavioral standpoint.

The dates in question are the Middle Stone Age and Late Stone Age in Africa -- 300,000 to 30,000 years and 30,000 and 10,000 years, respectively. The equivalent stages Europe, Asia, and North Africa are known as the Middle Palolithic and Upper Palolithic, and all deal with the tool assemblages of specifically anatomically modern human populations first explored in Chapter 12. Figure 16.7 (p. 430) nicely summarizes the findings of these stages in different areas of the old world and the tie between the origin of Homo sapiens, the environment, and complex behaviors.

Regional Patterns in the Archeology

European evidence: The transition in Europe is known as the Upper Paleolithic revolution, which coincides with the first appearance of modern humans to the region that carry the cultural traditions that are known as Aurignacian. This happened about 40,000 years ago, according to radiocarbon evidence in northern Spain and it includes blade-based technology and the use of bone, ivory, and antler for points as well as body ornamentation. As the upper Paleolithic progressed, so did temporal and spatial variability of style and the foundations of cultural traditions as we know it today for the Aurignacian.

Asian evidence: The Middle East provides evidence as a natural migration route between Africa and the east and evidence exists from at least 200,000 to 50,000 years ago of Neanderthal, early modern, and other hominin populations. The scarcity of sites in Asia make it difficult for scientists to interpret behavior and tool use, but evidence does suggest significant differences between the east and the west of the continent – further evidence for the out of Africa hypothesis, with the possibility of multiple dispersals of hominin populations.

African evidence: Sub-Saharan Africa should hold the evidence for the evolution of modern human behavior for the out of Africa hypothesis to hold true. This is important not only for finding the earliest date of modern human tool-using behavior, but also include transitional steps in line with dispersals to other parts of the world. In sum, archeological evidence should mirror scientific presuppositions. Figure 16.11 (p. 439) shows the evidence collected towards explaining ‘modern’ African behavior – but the archeological record is very sparse in comparison to Europe, leading scientists to find very little early symbolic behavior in contrast to European findings. This is because of, as Alison Brooks (and the authors) argues, the unfavorable conditions for preservation in Africa and the little amount of sites actually investigated.

-Although the anatomical and genetic evidence is strong for the out of Africa hypothesis, does the lack of archaeological evidence give credence to the multiregional hypothesis believers? Is it fair to assume past African behavior although the archaeological evidence is by no means complete?

Toward an Integrated Model of Modern Human Origins

The authors argue for a ‘multiple-event, multiple-dispersal’ model to build on the out of Africa hypothesis. This is based on a few interrelated premises supported by evidence presented thus far:

- All living humans are descended from a relatively small population from Africa (in all probability) dated to approximately 150,000 years ago.

- Hominins outside that population, be they archaic or modern, have not contributed significantly in genotype or phenotype to the modern population – all consistent with the notion that the modern population from Africa colonized and replaced all other populations.

- The ‘origins’ of modern humans are not based on a single event, but rather spread over the last 200,000 years towards the development of anatomical modernity in Africa.

- Multiple dispersals explain the spread of modern human populations around the world.

- Modern humans share their evolutionary origins in archeological terms of the ‘Mode 3 industries of Africa’ with the Neanderthals. Behavior is shifted in cultural terms rather than biological or genetic.

- Not all archaic hominins are the same.

These premises are all related to the ‘principles of evolution’ outlined by the authors (p. 444): the importance of geography, the role of the climate, the role of behavior, the importance of microevolutionary processes, and the importance of extinction in explaining all evolutionary process and change.

-The authors discuss the need for complexity in understanding human evolution as opposed to the simplicity that Darwinism offers. Is human evolution that much more complex or are we as susceptible to the same evolutionary processes that affect all of life? Is it possible that our belief in the complexity of our evolutionary history is a reflection of our unique ecological niche as a big brained, socially dependant species? For example, what would Canis familiaris say about its own evolutionary history if it could?

Part II: Chapters 12 and 13

Chapter 12: Behavior and Evolution of Early Hominins

The Archaeology of Stone Tools

Instead of stone tools being studied as the focal point within a system of typologies, or types of types, the study of artifacts within a context of subsistence strategy has become the current trend. Archaeologists study artifacts including chipped stone tools as a method of determining not only individual tool function, but they use their analysis to answer larger methodological questions relating to subsistence practices. One way of determining function is by practicing the methods and techniques that were used to create the original artifact. This type of research is called experimental archaeology. There are 5 modes of defined stone tool assemblages: Mode 1. Oldowan (chopping tool), Mode 2. Acheulean (uniformly flaked bifaces), Mode 3. Prepared Core (Levallois-micro flaking), Mode 4. Blade ( Upper Paleo, Later Stone Age), and Mode 5. Microlith(Mesolithic, small, delicate tools). The different modes of stone tool technology appear at different periods, but often continue to be utilized in later stone tool assemblages. Simple chopping tools of the Mode 1 kit can be found in the archaeological record up until the late historic periods in North America. Tool kits like the Oldowan and the Acheulean have a persisting utility based on their multiple functions and ease of preparation.

The Earliest Known Tools-

At approximately 2.5 mya, the oldest recorded stone tool artifacts appear in the archaeological record. They have been recorded at several sites, but the technology is named after the Oldoway Gorge in Tanzania (Those Leakeys are everywhere). Four categories of stone tools were created from Mary Leakey’s research: tools, utilized pieces, waste, and manuports. It is important to point out that the assemblage variety attributed to the Oldowan are more of a result of opportunistic production (p.312); artifacts tend to blend in one another typologically as a result. Utilized pieces tend to resemble waste, and scraper tools and choppers are often the product of flake production through various types of percussion. Manuports are pieces of rock that have been carried to a site, but have not been modified. They are frequently comprised of materials that could be used as percussion tools or could be percussion flaked into a chopper or scraper. Early hominins may have used a variety of materials such as antler, bone, or wood, but preservation in the archaeologicical record is poor for those material types. The stone tools associated with early hominin use have wear patterns indicating they were used for a range of subsistence activities such as butchering, wood-working, and plant processing (p.315). The broader implication for the Oldowan technology is nothing short of one of the most significant technological revolutions that may have contributed to further encephalization (p.315).

How has the discovery of Homo Floresiensis redefined the correlation between brain size and tool production capabilities since they had a tiny brain yet potentially created advanced stone tools?

The Kanzi Experiment: Oook oook oook!

In addition to the debate that pits Australopithecus against early Homo, a debate exists over whether apes have the physical and cognitive ability to create stone tools. The cognitive demands and physical structure of the arms, wrists, and hands were studied in Kanzi, a captive bonobo. Although Kanzi was able to produce stone tools, the lithic product differed from the Oldowan assemblages. The studies failed to determine if Kanzi’s poorer performance reflected differences in cognitive ability or anatomical constraints (p.317).

A frequent argument resides regarding the identity of the hominin responsible for early stone technology. The two representative and contemporaneous hominins are Homo and Australopithecus. By comparing hand morphology, pro-Australopithecus advocates such as Randall Susman conclude that later robust australopithecines had the manipulative ability based on hand morphology to create stone tools (p.318-319). It is possible that both species were able to produce stone tools and something led to technological expansion in the genus Homo.

Tool technology appears to have expanded, but did not necessarily originate, along a parallel gradient with the brain. What different hypotheses might be able to account for this parallel expansion? What adaptive strategies (e.g., resource intensification, niche exploitation, predation defense, warfare…) would have been well-suited for the implementation of stone tool technology?

The Pattern of Early Hominin Evolution-

The understanding of early hominin evolution continues to be elusive, but what is clear is early the early phase of hominin evolution was not a straight path to Homo sapiens (p.320). Rather, it was a result of a series of adaptive radiations in which early hominins expanded geographically, adapted to and exploited different habitats and niches, and underwent varying specializations including evolutionary reversals. The origin of the hominin clade is currently established somewhere between 7 and 5 mya and may have been the result of an earlier adaptive radiation of the African apes. A second radiation was likely responsible for the diversification and geographic expansion of gracile australopithecines in Africa. A third dispersal may have resulted in the emergence of the robust australopithecines. The fourth potential radiation may have been linked to early species of Homo. The resulting picture of early hominin evolution is that of a bush (p.323); it represents a continuity of events where several dispersals led to multiple species coexisting throughout Africa during different periods. This would be a fine example of punctuated equilibrium.

Homo represents an example of a reversal in the evolutionary trend of megadonty although the causes for this reversal remain contested (p.326). Other evolutionary trends that help create the clade include larger cranial capacity and reduced dentition. More recent analyses (p.326) indicate when other factors are included with a more focused cladistic method, the adaptive shifts that signify the Homo genus actually occurred later with Homo ergaster. Homo habilis and Homo rudolfensis would actually be more cladistically similar to Australopithecus. This would create a definitive gap that may signify a major adaptive change that led to the evolutionary success to later species of Homo. If the turnover-pulse hypothesis is correct, major climate shifts would have lead to origination/extinction events, and major climate changes would have resulted in detrimental/opportunistic changes in ecological relationships. In the paleontological/archaeological record, adaptive radiations in early hominins reflect adaptive strategies from an ecological perspective. During particular periods associated with events of adaptation, early hominins adjusted to and exploited ecological niches through adaptation and specialization in terms of geographic distribution, behavior, and diet.

What underlying factors could be responsible for the multiple adaptive radiations and specializations that occurred in African apes and early hominins? The authors provide a few potential factors for each radiation. Can you think of any other potential factors and/or related specializations? The turnover-pulse hypothesis argues that extinction occurs after origination. Is there any evidence in early hominin evolution that supports/debunks this argument?

Chapter 13: Africa and Beyond: The Evolution of Homo

Evolutionary Patterns-

The species Homo erectus has undergone several name changes since its discovery in 1887 by Eugene Dubois on the island of Java (p.332). Initially regarded as the “missing link” in human evolution, Dubois named the fossil specimens considered to be from the same individual Anthropithecus erectus. He changed the name to Pithecanthropus erectus after believing the “missing link” had been discovered based on cranium measurements (p.333). The classification as the link between apes and humans was based off a single top of a hominin cranium and a complete femur although the femur is now thought to be that of a later species Homo sapiens (p.334). Peking man was discovered in 1927 by Davidson Black and was subsequently named Sinanthropus erectus (p.334). In 1951, both species were combined in to a single genus and species Homo erectus because of their greater similarities to Homo sapiens (p.335).

The oldest known and most complete fossil specimens have been recovered in the Lake Turkana region of northern Kenya and are around 1.8 million years old (p.336). Of significance is the brain size which is larger than Homo habilis by approximately 210cc at 850cc.

One of the most important discoveries for Homo erectus was the complete skeleton of a H. erectus boy on the west side of Lake Turkana. The importance is two-fold: many of the postcranial elements of Homo erectus had not been discovered, and it allows for overall body proportions and their relationships to be scrutinized (p.337). The anatomical relationships allowed paleoanthropologists to make inferences about ecological and behavioral factors attributed to the species such as life-history, subsistence, and language capacity (p.337).

Changing Views: Dates and Evolutionary Pattern-

Two views of Homo erectus have appeared as a result of the quantity of fossil specimens that have been collected (p.339). The first conclusion is that anatomical variations initially observed in Asia seem to quickly spread everywhere. The second conclusion declares that Homo erectus originated in Africa around 2 million years ago and dispersed outside Africa around 1 million years ago. The possibility that H. erectus took around 1 million years to disperse provides an important puzzle in the history of H. erectus (p.339). One of the reasons for delay may be considered on technological terms. It is suggested (p.339) that Homo erectus lacked sufficient technological development needed to expand their geographic range outside of Africa until the development of the Acheulean industry around 1.4 mya.

What are the implications of the gap in time between Homo erectus’s appearance and eventual expansion out of Africa? Current evidence (p.339) suggests that either there was no delay between evolution and dispersal of Homo out of Africa, or Asia was the origin of H. erectus at 2 mya. Recent analysis of the Modjokerto skull from Java determines the age to be between 1.8 and 1.6 million years old and is highly suggestive of an Asia origin although the actual provenance of the skull is in question (p.340). Another find in China in 1988 may also offer a precursor to H. erectus dated close to 2 mya (p.340). Both of these finds reinforces the hypothesis for an “out of Asia” origin tale of H. erectus although most still consider that H. erectus is descended directly from Homo habilis/rudolfensis approximately 2 mya in Africa (p.341).

Changing Views: Anatomy and Evolutionary Pattern-

Many anthropologists support that Homo erectus may represent multiple species based on variation viewed between separate geographically distributed populations (p.342). Homo ergaster is the new species in which the earliest African specimens have been assigned. The relationship between ergaster and erectus is considered to that of an ancestor and a descendant (p.342). This analysis continues to support the hypothesis for the origin of Homo from Africa and it attributes the appearance of H. erectus in the archaeological record in Africa as a second later dispersal from Asia back to Africa (p.342).

Some of the key anatomical elements observed in H. ergaster/erectus that differ include several differences but two appear to be significant. The first trait is the increase in brain size over time from ergaster to erectus between 850 and 1100cc. It appears to be a significant increase, but the body size increased from ergaster to erectus as well indicating that the relative brain size may have only increased minutely (p.342).

The second trait has implications for the understanding of behavior such as subsistence strategy (p.343). Homo erectus marks the initial appearance of a human nose with the nostrils facing downward which permits moisture to condensate from exhalation which would have been important in active subsistence on in a warm, arid environment (p.343).

Several other behavioral inferences can be made through the larger body size, decreased sexual dimorphism, a more robust and heavily muscled structure (compared to modern humans), and the absence of an expanded neural canal in the lower thoracic vertebrae indicate the following: Homo ergaster/erectus was subjected to routine heavy exertion, possessed an broader-ranged subsistence pattern, had less male competition, and did not possess spoken language (p.343-344). All of these traits may assist in the understanding of the behavioral ecology of H. ergaster/erectus. What sort of ecological model would be sufficient in accommodating the aforementioned trait? The authors (p.343) mention the possibility that H. ergaster/erectus may have participated in male-male cooperation. What significance would this have on the origins of modern human behavior and social structure?

Changing Patterns of Behavior-

A number of changes occurred within the genus Homo during the period that ergaster/erectus lived. The following is a list of behavioral adaptations attributed to the initial appearance and subsequent existence of ergaster/erectus (p.344):

• The first appearance of hominins outside of Africa, although other evidence may argue for Asian origins (p.340-341).
• The first appearance of systematic hunting (broader subsistence patterns and decreased male-to-male competition are possible evidence).
• The first appearance of early “Home bases”( May mark an increased sedentism, intensified resource tethering, increased social behaviors e.g. cooperation).
• Toolmaking becomes systematic (indicates increased cognitive ability and manipulation (p.345)).
• The initial use of fire.
• The first indication of an extended childhood (smaller birth canals, earlier births resulting relatively unformed brains, and the demand for social learning are factors).

In addition, life histories change from being an apelike pattern to more towards modern Homo sapiens although H. ergaster is considered intermediate of the two (p.345).

An increase in the frequency of faunal and lithic evidence in the archaeological record from early Homo through H. erectus occupations indicates hunting activity (p.345). One of the significant developments attributed to the appearance of H. ergaster/erectus is the intensification and innovation of stone tool production evident in the Acheulean Industry (mode 2 technology). The teardrop or ovate shaped handaxe is the flagship for the Acheulean tool industry (p.346). Larger tools also appear that appear to be more specific in function. What is important in the Acheulean kit is the systematic flake reduction and core preparation process as it reflects a higher level of both cognitive and manipulative ability in the conception, process, and finished product (p.346). The Acheulean technological period represents a long period of continuity with a wide geographical distribution lasting from approximately 1.4 mya to 200,000 years ago (p.346; 348).

The Movius line is a boundary between the distribution of bifaces and non-bifaces lithic tool industries (p.349 see figure 13.15). It geographically separates Africa, western Asia, and Europe from eastern and southern Asia. Bifacial reduction is nearly exclusive to the west half (observe the hybrid zone in fig. 13.15). Bifacial reduction of a stone tool means that lithic material has been removed from both dorsal and ventral sides of a core or large flake from a core. Usually this is done in some observable and systematic fashion ending in a thin, finely flaked tool. What potential causal factors can be responsible for this line?

Subsistence Practices and Settlement Patterns: Behavioral Ecology

Several hypotheses have been developed regarding early hominin subsistence development and strategies including the home-base hypothesis, the food sharing hypothesis, the scavenging hypothesis, and the advanced scavenging hypothesis (p.351-359). There is a debate that focuses on “hunting versus scavenging,” or “Man the Hunter” versus “Woman the Gatherer.” It appears that advanced scavenging may have been more feasible from both a technological and an ecological standpoint for hominins although they would have differed from the concept of modern hunter-gatherers (p.359).

Cutmarks and percussion fractures on fossil bones observed in the archaeological record and sites indicate early hunting or scavenging practices associated to the earliest signs of meat processing and consumption as early as 2.5 mya (p.359). The increased consumption of meat is considered an important factor in human evolution (p.360). Did dietary changes lead increased social behaviors such as material transport, resource intensification, and new subsistence strategies? Does the increase in modified faunal remains associated with lithic material suggests cooperation in resource procurement visible in the archaeological record as “kill sites,” or does it represents Homo as a scavenger?

NEW SIVALADAPID PRIMATES FROM THE EOCENE PONDAUNG FORMATION OF MYANMAR AND THE ANTHROPOID STATUS OF AMPHIPITHECIDAE

Fossil primates from the late middle Eocene Pondaung Formation of Myanmar have been used to construct the evolutionary history of anthropoids. However, the most abundant anthropoid fossil currently used from the Pondaung Formation have proven to be controversial in reconstructing the evolutionary tract. This article describes the findings of two new primate fossils, Paukkaungia parva and Kyitchaungia takaii for the middle Econene Pondaung Formation of Myanmar. The fossil remains of the lower dentition from both Paukkaungia and Kyitchaungia are closely related to other sivaladapid primates. Therefore, these new findings, for the first time, are able to document the presence of adapiforms in the Pondaung Formation, and enhance the taxonomic and paleoecological diversity of the late middle Eocene primates of Myanmar.



Beard, K. C., Marivaux, L., Soe Thura Tun, Aung Naing Soe, Chaimanee, Y., Wanna Htoon, Marandat, B., Htun Htun Aung, and Jaeger, J.J. 2007. New sivaladapid primates from the Eocene Pondaung Formation of Myanmar and the anthropoid status of Amphipithecidae. Bulletin of Carnegie Museum of Natural History 39: 67-76.

Proximal Femoral Anatomy of a Sivaladapid Primate From the Late Middle Eocene Ponduang Formation (Central Myanmar)

Proximal Femoral Anatomy of a Sivaladapid Primate From the Late Middle Eocene Ponduang Formation (Central Myanmar)
2008

By: Laurent Marvaux, K Christopher Beard, Yaowalak Chiamanee, Jeans-Jacques Jaeger, Bernard Marandat, Aung Naing Soe, Soe Thura Tun, and Aung Aung Kyaw

Printed in American Journal Of Physical Anthropology 137:263-273.

This article examines the morphology of a proximal femur recovered from the Ponduang formation in central Myanmar. The proximal femur is part of the hip joint “which supports the weight of the body in both static and dynamic postures” (pp 269). The specimen that was utilized for analysis was well preserved and represented a significant portion of the femur. From the measurements that were obtained the research team was able to discern features such as, the creature was a proficient leaper which is evident because the “overhang of the trochanter” would have provided more leverage (pp270). Another characteristic of the femur suggested that the creature was able to freely move its hip a possible sign of climbing. In general these features suggested that this primate was “engaged in a kind of active arboreal quadrupedalism with some degree of proficiency” (pp 270).
What is interesting about this specimen is that in the Pongduang formation only two primate clades had been previously identified; the eosiimids and the amphipithecids. However, this new specimen exhibits characteristics of adapiforms and extent strepsirhines. This, in turn, challenges what was previously thought of this area and suggests that there was a greater diversity of primates in the area than previously thought (pp 263-265).

Earliest Complete Dentition of an Anthropoid from the Eocene

A new species located in the Yuanqu Basin, Shanxi Province, China named eosimias centennicus has shed light on the formation of early primates. The specimens collected of this small primate include a complete lower mandible (only lower left incisors missing) never before found. The information stemming from this dentition confirms anthropoid affinities of Eosimiidae, which in turn gives new data of an earlier structural step in the origin and evolution of higher primates despite its primitive characteristics. Given this new information geographic assessments can be made; it can be argued that by the mid-Eocene there were present higher primates living from Algeria to eastern China.

Beard, K Christopher, Tong, Yongsheng, Dawson, Mary R, Wang, Jingwen, Huang, Xueshi.
"Earliest Complete Dentition of an Anthropoid Primate from the Late Middle Eocene of Shanxi Province, China" Science. Washington: Apr 5, 1996, 272(5258) pg. 82-85

Evidence for Anthropoid Origins

Chris Beard is a chief proponent of the "Out of Asia" hypothesis for anthropoid (monkeys, apes and humans) origins. His latest find, Ganlea megacanina, offers further support for this idea and Beard presents this evidence in an article published in the Proceedings of the Royal Society B this past July. The article discusses the specifics of the dental morphology of Ganlea at length and compares its features with those found in extant primates inhabiting the New World. The similiarities between the fossil and these NWM centers around atypical apical wear patterns on the lower canines that are consistent with diets which include hard, tough fruits that contain seeds. The new fossil species also exhibit a high level of canine robusticity not found among the other amphipithecids, members of the Amphipithecidae family, but do show apical wear patterns similar to those of Ganlea. This variation in canine robusticity is also found among extant pitheciins. The adult body mass of Ganlea was estimated at about 2 kg utilizing Glenn Conroy's mass estimation based on the area of the first molar of primates. This weight is comparable to that of the white-faced saki monkey (Pithecia pithecia) pictured below. The link to Beard's article is also below.



Article: http://rspb.royalsocietypublishing.org/content/276/1671/3285

Chapter 9: Searching for the First Hominins

Chapter 9: Searching For The First Hominins

Genetic evidence suggests that the Hominin clade arose 5-7 million years ago (pp 229). This chapter deals with attempts to identify the earliest hominins.

The Moving History of the Missing Link
The missing link, transitional species between apes and humans, has changed throughout history. Initially it was thought to be Homo neanderthalensis, but we now know that they were relative late comers in history. Next Pithecanthropus erectus was thought to be a possible candidate for the “missing link”; it exhibited many apelike and humanlike characteristics. The point here is that since the idea arose of missing links that the dates have been pushed back considerably from roughly 150,000 years ago (Home neanderthalensis) to between 6 and 7 million years ago, with the discovery of Sahelanthropus tchadensis. This specimen is congruent with what genetic evidence is telling us, and furthermore it was found in Africa, which is also parsimonious with what most paleoanthropologists believe.

Major Sites of Early Hominin Fossils: South Africa, East Africa, and West Africa
All of the early Hominin sites are located in Africa, such a Laetoli and Hadar. Research initially took place in South Africa and sites such as Sterkfontein were discovered. It was conducted by researchers such a Raymond Dart and much of the research was conducted in cave sites and lime quarries. In South Africa such specimens as Australopithecines, noting there is two separate species, a robust form and a gracile form. Whatever the case this clearly suggests that two hominids lived at the same time and thrived in South Africa.
Attention then shifted to East Africa and was primarily conducted by the Leakys. Sites that were identified here consisted of Olduvai and Lake Turkana. The specimens that were discovered here consisted of Homo habilis, Australopithecus boisei, Homo erectus, Homo ergaster, and Australopithecus aethiopicus.
Until recently fossils were only discovered in South and East Africa. However, important discoveries have been made, for example what is possibly the oldest known hominin, Sahelanthropus tchadensis, was discovered in West Africa.
All of this evidence suggests that early hominins evolved in Africa, and mot scholars agree that they didn’t spread out until roughly 2 million years ago, when Homo erectus decided to take a nice long stroll north.

The First Hominins: Current Contenders –Orrorin, Ardipithecus, and Sahelanthropus
It has been suggested that a good contender for the earliest hominin should be 5-8 million years old and located in Africa. There are three reasonable contenders.
Orrorin: dates about 6 million years old, shows evidence for bipedalism, but exhibits apelike dentition. It was discovered in Kenya.
Ardipithecus: was discovered in 4.4 million year old contexts in Ethiopia, However, earlier specimens have been dated to about 5 million years ago. It also exhibits evidence for bipedalism, however retains apelike dentition.
The last contender is Sahelanthropus: discovered in Chad and is estimated to be 6-7 million years old. It has a hominin like facial structure, reduced canines and thick enamel. It is also possible that it was capable (at least to a certain extent) of upright locomotion. However the remainder of its features are apelike, such as a small rounded cranium and brain, much like a chimpanzees.
What all of this suggests is that Hominins were incredibly diverse and that many co-existed with one another.

Bipedalism
Bipedalism and Human Evolution
There are four characteristics that are important to the human condition, bipedalism, increased brain size, change in dental structure, and the development of culture. However, these characteristics developed at different rates. A key marker of early hominins was the ability to perform bipedal locomotion. Therefore, it is important to understand bipedalism in order to understand hominin evolution (pp240).
Bipedalism is interesting because of the form that it takes is unique to hominins. However, it is also tied to the assumption that bipedalism was essential for the development of tool because it freed the hands. But we have discussed other species that make use of tools that are not capable of bipedal locomotion to the extent that hominins were, such as tool using finches and chimpanzees.

Biomechanics of Bipedalism
There are two characteristics that distinguish hominin bipedalism from chimpanzee bipedalism. The first is that chimpanzees are unable to extend their knee joints. The second is that in bipedal locomotion the center of gravity must shift to the supporting leg and in chimpanzees this is not possible, due to femur structure among other things (pp242-243).
There are a number of adaptations that must occur for bipedalism to be possible.
-curved lower spine
-shorter broader pelvis and angled femur
-lengthened lower limbs and enlarged joint surfaces
-extendible knee joint
-a platform foot, which aligns the big toe with the other toes
-a movement of the foramen magnum toward the center of the basicranium

Ecological Context of the Origin of Bipedalism
It is important to understand that bipedalism was a shift from vertical clinging and leaping, to quadrupedalism, to bipedalism. The environmental context would have to be one that made it advantageous to walk upright and to give up brachiation.

Development of ideas on the Origin of Bipedalism
There are various ideas about why bipedalism developed: it allows for greater stamina, improves predator avoidance, increases thermoregulatory efficiency, warning, a shift in diet/ eating habits, the ability to carry things, and aggressive/impressive displays.

Energetics of Bipedalism: possible implication in its Origin
The development of bipedalism may be linked to changing environments and the availability of resources. Bipedalism is more energy efficient; it allows the hominin to make the most efficient use of their food resources. This type of environmental pressure may explain why hominins developed bipedalism initially. It also allows for a greater distance to be covered by the hominins, which would be necessary if resources were scarce.

Thermoregulation and Bipedalism
Bipedalism reduces the surface area of the body consistently exposed to the sun. This may also be linked to the loss of hair. In an environment where the sun is always beating down it ultimately is advantageous to develop adaptations that aid in regulating body heat.

Time and Energy: the Ecology of a Bipedal Hominin
No adaptation is perfect so in becomes increasingly important to evaluate the cost and benefits of different forms of locomotion. This allows the researcher to understand under which types of conditions bipedalism may be an advantageous adaptation. For example being well adapted for life on the ground makes one less suited for life in the trees.
The major issue that is addressed is not that bipedalism is a uniformly advantageous adaptation, but in what circumstances do the advantages outweigh the disadvantages. This makes it apparent that hominins were at least spending more than half of their time on the ground.