Reconstructing Ancestral Lifeways Using Humans and Non-Human Primates
Finding out what early hominids actually
did and how they acted is a tricky task, particularly since it is
difficult to imagine what the actual landscape might have been like
hundreds of thousands - or even millions - of years ago. While the
fragmentary remains of the past are often ingeniously interpreted by
researchers, additional information is often required to corroborate some
of the conjectures which arise. Two additional ways in which ancestral
pathways are examined rely upon ethographic and ethnographic
comparison.
Ethographic comparison relies upon
inferences drawn from animal studies, especially those of the African
Great Apes (i.e., gorillas, chimpanzees and bonobos). While none of the
ape models are expected to provide exact replicas of hominid behavior
(since apes themselves are very derived forms), the likelihood of some
models can be tested through field observation. Consistent approaches by a
majority of primate groups to particular ecological dilemmas strongly
suggests that response to be a likely scenario in hominid evolution as
well.
Ethnographic comparison draws upon human
behavioral variation through the study of different cultures. Again, while
no existing societies are expected to conform to an exact hominid
lifestyle (no modern humans living today are evolutionary throwbacks),
many insights have been made through the study of hunter-gatherer
social groups. The fact that there appear to be many commonalities between
culturally different hunter-gatherer societies suggests that ecological
constraints often provoked similar responses from different people in the
past.
Early Hominid Environment and Ecology
Paleoecological
reconstruction is possible through the study of correlates to
environment and ecology. Plants and animals which existed in particular
types of environments are carefully extracted and catalogued as
fluctuations inthe biosphere over a period of time. Added to this is the
use of oxygen isotopes, which
indicate worldwide temperature fluctuations. More recently, analysis of
aeolian (wind) dust deposition has provided a more detailed record of
climate change and seasonality. All of these forms of evidence point
towards an increasingly cold and dry environment with greater seasonality
during the late Miocene and Pliocene eras. Reduction in forested areas
most likely spelled to end for many Miocene hominoid species. The hominids
successfully adapted to open savanna and woodland environments, developing
a series of different strategies for predator defense, foraging, and
social behavior. One of these behavioral adaptations was possibly a shift
to accomodate quantities of meat in the diet, to augment plant resources.
Meat Eating, Cooperation, and Seasonality
The inclusion of meat in the hominid diet has
long been cited as a prominent factor in the evolution of human-like
social organization. Many of the earlier theories took this concept and
ran with it, from Robert Ardrey's portrayal of the Killer Ape, to the
"sanguinary habits" which convinced Raymond Dart of our
evolutionary history of bloodlust. From a more contemporary functional
ecological perspective however, meat is a precious commodity for modern
hunter-gatherers, providing a bonanza of calories and proteins which are
otherwise difficult to acquire. The desirability of meat, however,
obscures the reality of day-to-day existence: hunting parties, more often
than not, return emptyhanded. Bearing that in mind, there are two factors
which make a system of foodsharing desirable - if not absolutely necessary
- for a reliance on meat in the diet to be feasible:
- high payoff for success: success
often brings enough food for the entire social group
- low individual success rate:
successful hunts are likely unpredictable and irregular, making
success for any individual hunter relatively low at a particular point
in time
These conditions suggest that a network of
foodsharing would greatly benefit all participating parties by providing a
buffer against starvation (or malnutrition) due to individual
irregularities in success. Such a system would be an obvious example of
reciprocal altruism, where individuals who did not participate in
foodsharing were rapidly excluded from subsequent events.
An additional factor influencing the
increasing amounts of meat in the hominid diet may have been accentuated
seasonality in the environment. The dry season decreased resource variety
and abundance, causing many animals to divert their foraging strategies to
exploit more of a single food item, or a greater variety of foods they may
not have sought out before. These might include underground storage organs
in plants, nuts, or other specialty food items to compensate for an
overall decrease in resource abundance. Robert Foley (Cambridge
University) proposed that during human evolution, two modes of adaptation
were exercised by the hominids. The robust Australopithecines developed
masticatory specializations which allowed them to exploit tougher plant
materials, while the more gracile species relied upon a diversified diet -
which included more seasonal meat consumption.
Archaeological Evidence
Much of the archaeological evidence also
points to a shift in dietary composition, although direct evidence of meat
eating is rarely found. Insted, meat eating has been inferred from many
different sources. One source is through the interpretation of presence
and quantity of different skeletal elements found in living floors
(supposed places of hominid occupation). High densities of bones found in
association with stone tools have led researchers to believe that
processing and consumption of carcasses took place at these sites.
However, interpretation of this information can often be misleading,
particularly if taphonomy has not been adequately investigated.
Accumulations of bones and stone tools, while intriguing as evidence of
hominid meat-eating, could also be the result of unrelated processes.
Careful examination of the surrounding matrix is required to determine
depositional integrity.
Sites from Olduvai Gorge examined in this
manner suggest that site accumulation was not a by-product of river
deposition. A number of the bones accumulated in the Olduvai Gorge sites
exhibit evidence of cutmarks made by stone tools. While it may be
difficult to distinguish between tool-derived cutmarks and other possible
agents of bone modification (e.g., carnivore toothmarks), examination
under high magnification shows a clear distinction between the two.
Grooves produced by tools often leave many smaller, parallel grooves in
the main cut, whereas carnivore marks tend to be smooth throughout the
trough.
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Additional
interpretations can also be carried out concerning the timing and
sequence of resource acquisition by examining which marks come
first. Assessing which marks (when marks from both carnivore teeth
and hominid tools are present) lie below and above can be crucial
for interpreting meat-eating behavior of early hominids. Were they
hunters, or merely scavengers of the remains of prey felled by
larger carnivores? The available evidence suggests that early
hominids engaged in both activities, although the evidence for
hunting and primary access to meat resources increases in later
levels (especially with Homo erectus). The impacts of this
behavioral change on the development and evolution of hominid
social organization have been profound, particularly in the realm
of cooperation within social groups. |
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