|
||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||
Stone Age symbolic behaviours: questions and prospects Andrea Vianello Introduction In the evolutionary perspective typical of biology,
the more complex something is the more recent it is. Thus, symbolic
behaviours and the complex symbolic systems they generate should be
very recent because they appear late in the archaeological record and
they are not very different from contemporary behaviours. Biological
studies demonstrate that different species of a certain family of animals
may co-exist without the need for one to be superior in absolute terms
to the others. However, in the case of humans, anatomically modern Homo
sapiens (AMHS or Homo sapiens sapiens), the absence of any human species
other than ours in contemporary times has always been interpreted considering
our ancestors less evolved, which translates in less intelligent considering
the primary characteristic of AMHS. What happens then if an archaeologist
unearths evidence of symbolic behaviours in the Middle Palaeolithic
or evidence of complex symbolic systems among the Neandertals? Was the
mind of our ancestors closer to ours than we would like to admit or
do we have a problem in defining symbolic behaviour? Perhaps both, as
we shall see. In the following sections we shall review some recent
developments on early symbolic behaviours and the search for the origins
of them. The behaviours recognised are undoubtedly advanced and find
no parallels in any known animal, suggesting that they are indeed a
form of human symbolic behaviour that needs to be explored. However,
the recognition of differences between the early and mature symbolic
behaviours will prompt a concise review of the state of research on
both biological and archaeological grounds of the advent of mature ("modern")
symbolic behaviours. This review of evidence will span nearly the whole
length of the Stone Age and include two parallel perspectives, the biological
and archaeological ones. Although there is no attempt to provide a detailed
and comprehensive summary of these studies, the resulting picture should
provide some of the least controversial elements that may help in assessing
any theoretical criteria on the determination of symbolicity. In the
conclusions this work will try to provide a contribution on the formation
and testing of theoretical criteria of symbolicity founded on the evidence
as a whole. In addition, some methodological and interpretive issues
will be explored as they come out throughout the sections. Searching the first symbol: red ochre In a recent paper (Hovers et al 2003), archaeologists
have reported about the use of ochre at Qafzeh Cave. The authors suggest
that human beings in the region demonstrate evidence of symbolic behaviours
because complex symbolic systems can be inferred from the archaeological
record as early as 92,000 years ago, in the Middle Palaeolithic. To
date, this may be the earliest case of symbolic behaviours known to
science. Red ochre was skilfully produced at Qafzeh Cave and probably
used in connection with burials, without having any apparent practical
function. There are a number of other depositions where red ochre has
been detected and in every case red ochre is apparently used in non-utilitarian
contexts. The hypothesis of red ochre being used as material expression
of symbolic behaviours is simply tested verifying that non-utilitarian
purposes were the likeliest. The criterion according to which non-utilitarian
contexts are the product of symbolic behaviours may seem weak from a
theoretical and methodological point of view, but is solid in practice,
as we shall see. In the case of Qafzeh Cave, a few ochre-stained lithic
artefacts have been recovered and suggest that the red hue had a symbolic
meaning. Hafting, the use of ochre as painting substance, medicine and
aid for hide tanning have all be considered (Hovers et al. 2003: 505),
but they remain unproven and unlikely primarily because red ochre had
been produced from cores of different mineral compositions that required
different processing to obtain always the same colour. If practical
reasons were paramount in the production of ochre, then variability
in the colour may have been resulted as part of experiments finalised
to improve both techniques and uses. We should also keep in mind that
the minerals processed looked differently at the natural state and no
selection by colour is apparent for the stone employed in tools-making,
which are rarely stained. The ochre is present in several layers of Qafzeh cave
dating from 100,000 to 90,000 years ago (Hovers et al. 2003: 501). In
later layers ochre has not been found, but there is still evidence of
human presence. This suggests that ochre, for some reason unknown to
us, was used only for a period, a fact that reinforces the interpretations
of red ochre as symbolic. In the period of use, the excavators argue
that an association between human remains, fires, and inedible molluscs
can be identified. They (Hovers et al. 2003: 508) note that "the
presence of human burials exclusively in the same stratigraphic block
as the ochre is more telling". The recognised burials of an adult
female together with an infant (Homo 9 and 10) and of an adult (Homo
11) with deer antlers, which possibly were a grave gift are used by
the authors to support that the individuals occupying the cave were
capable of symbolic behaviour already at that early time. Evidently,
burials and grave goods, if proven, are not only proof of complex behaviours,
but also proof of meditation, abstract thought and therefore cognition.
Red ochre would then add to the picture, but perhaps it would not be
determinant to recognise symbolic behaviours as early as the Middle
Palaeolithic. In the Levant, ochre is used again in the Natufian period,
dated to 12,700 - 10,500 years ago and remarkably again associated clearly
with burials (Hovers et al. 2003: 510). Not only there is a long break
between the two periods of use, but also two human species are involved:
Neandertals about 100,000 years ago and Homo sapiens sapiens in the
Natufian period. Early symbolic behaviours The clearest evidence of Palaeolithic symbolic behaviours
in the archaeological record is provided by funerary contexts. Only
a few burials of Neandertals in the Middle Palaeolithic are known. Middle
Palaeolithic burials are variable and range from the simple caching
of bodies to excavated graves, where grave goods were deposed. Pettitt
(2002: 8-9) proposes six categories in which these early burials should
be divided according to the complexity of the inhumation, but the first
category is reserved for naturally occurred caching. In trying to provide
some examples for each category, Pettitt has shown that a categorisation
of burials based on complexity often groups burials according to their
chronology. The earliest burials of his second category, the simple
caching of dead, may be dated about 250,000 years BP (e.g. burials at
Pontnewydd Cave dated 225,000 years BP), while the earliest burials
of the sixth and last category, named "ritualised burial",
date from 27,000 years BP (Pettitt 2002: 9). Qafzeh is placed on the
third category, named "simple inhumation". The funerary practice
and the use of colour as symbol are found together only from about 100,000
years ago, within a coherent framework of complex symbolic behaviours.
Separate antecedents for both can be traced in the use of ochre and
the caching of the dead, but earlier symbols do not seem to have been
part of a complex symbolic system or to constitute evidence of symbolic
behaviour. At Kebara Cave (Schwarcz et al 1989; Valladas et al
1998), Israel, there is one of the earliest and most convincing cases
of excavated grave and evidence of secondary activity as well. The grave
has been cut through two hearths in the underlying layer and according
to the excavators the posture of the body was such that the head intentionally
remained exposed. At a certain stage, probably after the decay of the
flesh, the head was removed by other humans. The intervention of a carnivore
animal has been ruled out on the ground that the mandible, hyoid and
a right upper molar were recovered from their correct anatomical positions.
This deposition dates about 60,000 years ago and may be seen as the
antecedent of later burials when secondary activity becomes common.
At Shanidar Cave, the few depositions found represent over 10,000 years
of activity as they date from 60,000 to 45,000-50,000 years ago. Pettitt (2002: 18) concludes "that the focus of
Neandertal social life was the body" and remains cautious on the
significance of any burial before 27,000 years BP. Despite some evidence
of symbolic behaviour, it seems that indeed the human body was central
to any symbolic activity, whether it was a burial or the processing
of soft tissues. Even the red ochre, because of its possible association
with blood, appears linked to the body. Moreover, all these symbolic
activities may simply replace natural ones. For instance, the use of
red ochre may have been seen as a replacement of flowing blood when
the death was not associated to blood loss, which may have been seen
as the natural way to die. For instance, the symbolic meaning of red
ochre in Qafzeh Cave has been interpreted as "death" (Hovers
et al 2003). In the same way, defleshing may be seen as the natural
occurrence for bodies, as the consumption of the flesh as meat if the
natural event observed was the activity of a predator or scavenger.
In that case, both proven defleshing and presumed cannibalism may be
seen as symbolic re-enactments of natural occurrences. Regarding symbolisms
connected to the body, it should be noted that both "life"
and "death" cannot be expressed without the use of symbols.
The red hue may have meant on occasion, blood, fire, flesh and meat
consumed at the time of death as well many other concepts. Thus, most
if not all of these concepts may have used to express the two terms,
while understanding that both are part of the ineluctable natural cycle
of fertility. The positioning of the body, the deliberate removal
of the head and the increasingly evident need to bury the dead in a
constructed space support the possibility that complex symbolic systems
existed. The use of ochre and the practice of burying the dead are not
homogenous in the form both in space and time during the Palaeolithic.
In particular, studies on red ochre (Knight, Power, and Watts 1995;
Power and Aiello 1997; Hovers et al. 2003) demonstrate the variability
of meanings. The handful of burials at Shanidar Cave spanning over 10,000
years are also evidence suggesting the absence of standardised rituals
in this period, though the several symbols of later rituals can often
be recognised. Burying the dead is a deliberate action that implies
extended social ties, strong enough to survive the occurrence of death.
Unlike red ochre, there is no possibility that such behaviour was initiated
to imitate something existing in the natural environment. In the case
of red ochre, the colour has been associated to various natural elements
of the same colour, such as blood. The use of colour is therefore understood
as a word in a language, a symbol meaning something which can be found
in nature. In the case of burials, accidental sepultures were unlikely
to be discovered easily and to have provoked imitative behaviours. Instead,
it is probable that burials were seen as a form of protection from scavengers,
but this care implies strong social ties with the buried individuals
and the thinking a relationship beyond death with those individuals,
which is evidence of elaborated cognition. Ethological observations have proved that mammals such
as the elephant or the polar bear recognise defleshed members of the
same species previously met and this triggers memories and behaviours
that can be described as grief or mourning, but this behaviour is always
strictly linked to the memory of specific individuals. The mammalian
behaviour stops short of burying the dead, which would be physically
possible, and therefore the action of burying the dead may be used as
proof of advanced cognition, well over self-consciousness. Symbolic
behaviours such as the presumed ochre-staining of the body or the proved
ochre-staining of tools and later of skeletons (e.g. Paviland Cave)
seem to be a by-product of advanced cognition. Symbolic behaviours stemmed
from the need of expressing abstract thoughts originated by a self-conscious
being relating with other individuals perceived as similar self-conscious
entities. Individuals burying the dead must have enough cognitive capacity
to separate themselves from the rest of the natural world, i.e. they
must be self-conscious. They also must have the cognitive capacity of
distinguishing the surrounding natural environment and recognising similar
members. Furthermore, they must have the cognitive capacity of understanding
that the other members of a social group are similarly self-conscious.
This means that the world was perceived as the self, the others and
the natural world. In burying the dead, a relatively simple and obvious
action for contemporary humans, Palaeolithic hominins demonstrated that
they understood and related to the others differently from the natural
world because in burying a dead they interpreted the will of that individual
and acted independently of a direct interaction or natural stimulus.
The hominins burying other individuals thought the dead would fear scavengers
or would like for any other reason (e.g. hiding, return to earth after
life-cycle, etc.) to be buried and this happened because they imagined
themselves in that situation. They then acted because in this mirroring
of the self into the other they probably hoped the same care would be
reserved to them and this may have helped them in overcome the fear
of death. However, the tripartite division of the world in self, others
and natural world is very complex and far from anything observed in
any animal. Accepting a mature cognitive capacity of hominins well beyond
self-consciousness, symbolic behaviours becomes therefore the language
through which unphysical ideas could be expressed. Thus, self-consciousness
must have appeared before graves, as early as evidence of caching the
dead, about 250,000 years ago and perhaps even earlier. Complex cognitive
capacity appeared probably after 250,000 years ago but certainly before
92,000 years ago, when at Qafzeh Cave there is evidence of symbolic
behaviour, which originates from complex cognition. Have AMHS individuals got their own symbolic behaviour? Language probably offers the best insight of the complexity
of human behaviour. However, direct evidence of language is very late,
though human language capable of transmit abstract and real meanings
seems to have existed as early as 60,000 years ago (Davidson and Noble
1993: 363). In seeking the very first evidence of language, burials,
symbols and several other traits the evidence points to a past when
the anatomically modern Homo sapiens (AMHS) had yet to be culturally
distinguishable and spread all over the globe. This causes a split between
the modern anatomy and behaviour. It is evident considering red ochre and burials that
Neandertals were capable of abstraction and complex symbolic systems.
Although it is still unclear whether the Neandertals merged with or
were replaced by modern humans, it is evident that the behavioural difference
between the two species was not very sharp at the time of co-existence.
The earliest evidence of modern anatomy is ca. 160,000 years ago (White
et al. 2003), but the earliest evidence of the symbolic use of red ochre,
one of the traits of behavioural modernity in a long list recently criticised
(Henshilwood and Marean 2003), dates not later than 230,000 years ago
and may be as old as 285,000 years ago (McBrearty and Brooks 2000, Barham
1998, Barham and Smart 1996). None of the traits (Henshilwood and Marean
2003) identified and perhaps not even a particular combination of these
may be able to define modern behaviour. This happens because the environmental
situation in which hominins lived was variable and therefore the traits
displayed do not seem to follow any repetitive pattern. A hypothesis
could be built on the basis that a pattern in the traits displayed is
the fingerprint of modern behaviour, but with no pattern available the
hypothesis is unsustainable. Furthermore, the context of deposition
is often badly preserved, leaving archaeologists to deal with partial
and unreliable information that would be difficult to use for testing
purposes. To sum up, the archaeological evidence proves that
hominins have had symbolic behaviours, but these varied for long before
some fixed patterns could be recognised. Thus, there are two different
periods in human history in relation to symbols. In the first period,
which predates AMHS, self-consciousness, the capacity of abstraction
and symbolic systems as well as a few of the traits used to describe
modern behaviour appeared. In the second period, patterns in symbolic
behaviours can be identified and the traits increase exponentially.
On one hand, there is no evidence that this change has been directly
fuelled by biological changes because the path bringing humans to use
symbolic systems began at the time of Homo heidelbergensis or perhaps
already the late Homo erectus and progressed in different species such
as Neandertals and Homo sapiens. On the other hand, it is evident that
AMHS progressed further than any other hominin, resulting in their definitive
evolutionary success. As a result, archaeologists can focus on either the
appearance of the first symbolic systems and behavioural traits or their
late organisation in ritualistic patterns. This division seems important
and evident on the archaeological record but it cannot be justified
on material culture alone because it would be just a change in culture.
In Europe, perhaps the best studied case, the arrival of Homo sapiens
with a more sophisticated culture in which the sophisticated art work
was included has prompted Henshilwood and Marean (2003: 635-636) to
argue that art work may be the decisive trait in distinguishing modern
behaviour, of which modern symbolic behaviour is a subset. However,
they point out that art work needs to be considered all over the globe
and when this is done, there is no evidence supporting a sudden arrival
of the behaviour associated with a specific species outside Europe.
They also suggest that rapid changes in the production of distinctive
and consistent artifact styles may provide the marker for behavioural
modernity. This brings us to the starting point where changes in material
culture would represent changes in behaviour, though in Henshilwood
and Marean's hypothesis only specific types of cultural changes could
be considered for this. Although this limitative definition helps in
considering human behaviour overall, when considering exclusively symbolic
behaviours we need to find a single change capable of accounting for
the emergence of modern symbolic behaviour in an archaeological record
punctuated with small changes. New prospects are offered by the human genome, which
may be used to find genetic changes dated about 40,000-30,000 years
ago according to Henshilwood and Marean (2003), or in the incertitude
of the date one specific gene that may be responsible for it should
be searched (Klein in Henshilwood and Marean 2003). Although not yet
feasible, this approach seems already doomed by methodological problems.
In the former hypothesis the link between genetic change and behavioural
change would be forcefully synchronised to a date obtained from the
archaeological record. In the latter hypothesis a single change at chromosomal
level would have had enormous effects abruptly. Even considering this approach from a purely biological
point of view, its weaknesses remain. Changes in brain capacities and
different human species cannot be detected in the archaeological record
very easily because changes in material culture are frequent and small
whereas changes in anatomy from an evolutionary perspective are far
in between. To this regard, the biological theory of punctuated equilibrium
proposed by Gould and Eldredge (1977) is born from the observation that
rapid periods of modification are distanced by long periods of slow
progress. This does not happen regularly in the archaeological record. The modern human anatomy first appeared at least 160,000
years ago, but until 40,000 to 30,000 years ago there is little evidence
of any difference in behaviour among the co-existing human species,
and the size of brain was very similar across species, particularly
AMHS and Neandertals, with the latter having the largest brains. This
means that it took at least 120,000 years for a change in the general
anatomy to become apparent in the archaeological record. Thus, finding
a chromosome that may have changed 40,000-30,000 years ago does not
ensure that the change it triggered has manifested itself immediately.
Moreover, there has not been a single important change 160,000 years
or so ago that simply manifested itself later, but a series of rapid
changes which then continue more slowly. In 120,000 years, the time
from the anatomical change to the appearance of behavioural modernity,
many genetic changes happened. The biological evolutionary system seems
to work like a cycle. Repeated environmental changes, new needs or any
other stable condition which would benefit from anatomical changes stimulate
modifications that may involve several alterations of the genetic code
at once, so that eventually a new species is originated. This is the
period of rapid change, which is followed by one of slow stabilisation
and progressive enhancement of the anatomy. This hypothesis would account
for both rapid biological transformations and progressive cultural variations.
During the rapid changes period the anatomy would adapt to suit the
new situation that prompted the change in first place, easing the burden
of everyday life without causing major behavioural changes. Instead,
the slow changes period would exploit the new possibilities offered
by the major anatomical transformations effectively causing shifts in
culture, style and behaviour, slowly and progressively. Modern symbolic behaviour may be defined as the symbolic
behaviour exclusive of Homo sapiens sapiens from about 40,000 years
ago and unparalleled for complexity in any other human species. Accepting
the hypothesis of evolutionary cycles, modern symbolic behaviour would
be the product of slow refinements within a framework of continuous
advancement, but it makes sense to separate it from a biological point
of view because it has been very stable, it has provoked no further
speciation and has reached a level of complexity unparalleled among
other human species. From an archaeological perspective it makes sense
as well because rituality appears coherently for the first time, while
art and symbolic systems become increasingly important. As we have seen,
both biological and archaeological considerations support the separation
of the modern symbolic behaviour from previous behaviours, but there
is no reason to claim a clear superiority of this behaviour from the
previous ones. From the first symbolic behaviour detected about 250,000-230,000
years ago to the earliest modern symbolic behaviour detected about 40,000-30,000
years ago there are 200,000 years in between of steady cultural and
behavioural progress. For instance, the Neandertals were probably behaviourally
very similar to the contemporary AMHS, and we may be fooled by the European
culture of the time that was not state-of-the-art until new people arrived
in the correctness of summing biological and cultural differences. On
one hand, it is likely that the Neandertals coped well for a while with
new cultural changes, perhaps as well as Barbarians coming into contact
of the Roman culture. On the other hand, the AMHS individuals bringing
new cultural elements had just developed them from a culture similar
to that still practised by the Neandertals, so that there was just a
small progress in between the two cultures. The large cultural gap we
see is partly due to the 30,000 or more years that separate ourselves
from both Neandertal and Palaeolithic AMHS individuals and partly to
the exceptional cultural and behavioural developments that were caused
by the combination of increased sociality and the exploitation of new
anatomical capacities. We shall now explore in more detail the cultural
and biological developments that made possible modern behaviour, and
particularly modern symbolic behaviour. Mature symbolic behaviours During the period from 40,000 to 30,000 years ago modern
human behaviours appear. A few examples will help in identifying some
of the commonest modern symbolic behaviours. Particular attention will
be given to burials in order to provide comparative material with the
earlier sepultures we have already examined. Three small animal figurines, made of mammoth ivory,
have been recently found at the cave site of Hohle Fels, in southwestern
Germany (Conard 2003, Sinclair 2003). One is shaped like a bird, another
like the head of a horse and the third may be half animal and half human.
Twenty other ivory figurines had been reported from the region previously.
Charcoal in animals painted in the Salle du Fond and the "horse"
panel of the Hillaire chamber in the Chauvet cave, France, have been
dated between 32,400 and 29,700 years ago (Valladas et al 2001). At
Dolni Vestonice one of the earliest "Venus figurines" known
is dated 26,000 years ago. Venus figurines, as they are called, become
increasingly frequent and peak at about 15,000 to 10,000 years ago.
They represent women, often pregnant, with exaggerated sexual attributes.
To the same period dates a male burial found at Paviland Cave, Wales,
which is known in the archaeological literature as "Red Lady of
Paviland" (Aldhouse-Green 2000). The skeleton as well as the grave
goods had been stained with red ochre. The grave goods consist of an
ivory rod, bracelet fragments and perforated periwinkle shells. Furthermore,
it is possible that two blocks of limestone marked the grave itself.
The cave was used by humans for long, perhaps sporadically, and great
quantities of Palaeolithic tools spanning from 35,000 to 11,000 years
ago have been recovered since the discovery of the burial, back in 1823.
However, the early date of discovery means that the context was inadequately
recorded, so that it remains unclear what the grave assemblage comprised. Since most of the Upper Palaeolithic complex symbolic
systems are attached to funerary activities, it seems useful to consider
the burial practice in the Mesolithic Levantine Natufian culture, which
is the earliest deliberate and systematic funerary practice known. The
Early Natufian period is significantly more recent than any other period
considered previously, dating from 12,500 to 11,000 years ago. In addition,
the population was largely sedentary or at least moving within a restricted
territory. This suggests that social ties played an enormous role at
this moment of history. Because the Natufian populations settled within
small territories, the range of social connections increased exponentially.
The original extended groups, typical of hunters-gatherers societies,
are still recognisable in death because the Early Natufian sepultures
were primarily group graves. The funerary practice seems initially motivated by
the attempt to preserve and show the unity of the original groups, a
need that implies a large society composed by several groups. The stable
settling in a territory produced a repetition of encounters between
the same individuals, creating a social network of interconnections.
This network produced a population in which each member was aware of
the others and the territory was the unifying element rather than blood
or the appurtenance to a group. The burials themselves ended up in reinforcing
the link between humans and territory, because the space in which the
people of Natufian culture was not only shared with other living humans,
but also with dead humans that not necessarily were connected to each
member. As a result an anthropocentric dimension of space replaced the
natural dimension in the minds of humans. The people of Natufian culture
lived in a human-centric space, where nature could be controlled to
some extent. The creation of a space by and for humans is not new however.
Early burials, both simple caching of corpses or deliberate sepultures,
are found in contexts extensively used by humans for very long times.
It is possible therefore that the sepultures were an attempt to mark
the territory as "human", to separate it from the natural
world. This hypothesis would also explain what linked sepultures thousands
of years apart: the location. Caves, providing shelter to the primordial
communities, were evidently the most obvious locations for social gathering
and probably the cradle of the concept of anthropocentric space. Grave goods, such as dentalium shells or bone beads
and pendants or fox teeth, occur relatively frequently among Early Natufian
burials (Belfer-Cohen 1995). The Early Natufian skull cache at Erq el
Ahmar (Neuville 1951), dated about 11,000 years ago, is the only evidence
of skull removal, which is common in the following Late Natufian period.
Kuijt (1996: 329) has produced an interesting table that summarises
some variables related to the burials across four consecutive periods
in the Natufian area, evidencing how each variable is dependent upon
the set of beliefs current at each time and location. Weinstein-Evron
and Ilani (1993) have reported the use of ochre at the site of el-Wad
Cave in Early Natufian layers dated 13,000 to 11,000 years ago. About
eighty earths of red, orange, yellow and brown local minerals containing
ferric oxide, silica or alumina as well as prepared ochre had been recovered.
Heating experiments on similar minerals (Weinstein-Evron and Ilani 1993:
466) demonstrated that in all cases the end-product would have been
red ochre. Grave goods, skull removal and use of red ochre are
just some of the variables that were part of the funerary rites practised
by the people of Early Natufian culture. Remarkably, the grave at Paviland
Cave, 26,000 years ago or the typical burial at el-Wad Cave 13,000 years
ago appear extremely similar in the presence of shells and bone or ivory
items as grave goods and use of red ochre. This similarity is even more
remarkable because Late Natufian burials are evidently different from
Early Natufian burials. The broad view that allows to recognise the
similarity in the symbolic systems used at Paviland Cave and el-Wad
Cave, which are far apart both geographically and chronologically, should
be expanded to include the whole Stone Age and Africa at least. We would
then notice that 96,000 years ago at Qafzeh Cave red ochre was skilfully
produced and human remains were possibly associated to inedible molluscs
(shells) and animal bones. In Middle Stone Age Africa red ochre was
also used (McBrearty and Brooks 2000). We may also notice how the practice
of skull removal appears and disappears throughout long periods and
vast distances. The simple fact that each variable appears and disappears
may be a meaningful pattern as well. For example, red ochre is used
at Qafzeh Cave 96,000 years ago when it had great importance, particularly
the specific red colour, but then it disappeared in later layers (Hovers
et al 2003: 494) and at Shanidar, on sedimentary grounds, seven adult
Neandertals "were deposited on separate occasions over at least
15 ka, i.e. from c 45-50 ka BP (Shanidar 1 and 5), to perhaps considerably
before 60 ka BP (Shanidar 4, 6-9)" (Pettitt 2002: 8). What is, if any, the difference between Palaeolithic
and Natufian burials? In the Middle Palaeolithic, several symbolic systems
were occasionally manifested and scarcely integrated, but there is no
evidence of a structured ritual. It is very likely that different groups
knew one or more of these symbols and handed them down generation after
generation, but they were apparently unable to combine them and hand
down the particular combination as meaningful per se. This happened
in spite of likely intercultural contacts between different human species,
suggesting that the problem was not the exchange, or perhaps sharing,
of complex symbolic systems among groups, but the capacity of expressing
beliefs was either missing (non-AMHS humans) or still immature (AMHS).
There was the capacity to express single meanings through symbols though. From about 40,000 years ago the frequency of contacts
among groups increased, perhaps because severe environmental conditions
may have reduced the range of mobility. The culture and behaviours of
neighbouring groups probably merged. There is no evidence of standardised
burials at first, which happens only very late, with the Natufian culture.
However, fine arts appear in their stunning beauty and art may suggest
that a biological change happened to make this possible. With the appearance
of art and then systematic burials, there is one element that is as
new as overlooked: repetition. For example, in cave art certain subjects
are repeated several times, in different places and at different times.
This repetition causes standardisation. Because several motifs-symbols
are "fixed", they are together and new ones seem to be born
as variant of those known. The capacity of creating new symbols from
other symbols appearing for the first time. The process occurring may
be described as "ritualisation". Any criteria we may use to
recognise modern symbolicity needs therefore to look for rituality.
This is a key discriminant between archaic basic symbols and mature
complex symbolic systems. Evolution and brain: the difficult relationship The burials of non-modern hominins already show that
many symbolic activities were practised, indeed all the main symbolic
activities in the Early Neolithic can be traced back to the Palaeolithic,
when these were apparently occasional. Complexity increases progressively
(Pettitt 2002) in the archaeological record because of the number and
combination of symbolic activities practised each time, not because
single symbolic activities appear more sophisticated. In short, it seems that non-modern burials tried to
recreate a natural scene adding some elements that were felt as missing
by the mourners. For example, the interment and use of red-ochre may
have been two symbols that recreated what were considered ordinary natural
occurrences, such as the natural covering and the loss of blood. The
physicality of the natural world was paramount, with the body being
at the centre of the scene and all the elements directly pointing to
natural occurrences in death. Palaeolithic minds materialised their
abstract thoughts into the physical world. People of modern symbolic
behaviour instead do not seem to have perceived the world directly through
their biological senses. They mediated the physical perception through
the I/self-consciousness and expressed their understanding of reality
through symbols. Modern symbolic behaviour in practice is the use of
symbols as words in a language; full expressivity was reached through
coherently structured symbols because the perceived reality was an abstract
belief. The archaeological record suggests therefore that a
significant change happened with the advent of modern symbolic behaviour
and this was driven by increased social contacts and produced complexity
only in the structuring of symbols, not their construction. The increased
sociality may have acted as a constant environmental factor that produced
changes at evolutionary level, but given the origin any change must
have interested especially the brain. However, the brain itself never
survived, so cranial capacity calculated from the skull is the only
data available. Remarkably, Neandertals reached a superior cranial capacity than the contemporary AMHS but AMHS only managed to achieve a full modern symbolic behaviour. Although minimal variations in cranial capacity do not affect intelligence, a reversion of any consolidated evolutionary trend may be explained only by a change in the relationship of the factors that in the first place started the trend. When the australopithecines employed primarily bipedal locomotion, the arms were increasingly free of their original burden of supporting the body and the secondary function, handling, became primary. Handling stimulated the brain and because early hominids were physically too small to support a brain capable of more intelligence, growth started naturally. The process peaked between 600,000 to 100,000 years ago. On this regard, it is interesting to notice how apparently the earliest Neandertals developed after the earliest AMHS, suggesting that the evolutionary trend of cerebral growth (table 1) continued in a progressive way, but for some reason the most "capable" brain in size was unsuccessful in the struggle for survival.
Table 1: comparison of cranial capacities The brain of AMHS decreased in size during Mesolithic in Europe
and Middle Stone Age in Africa (Henneberg 1998) and then continued the
trend of growth. Intelligence does not depend only on the volume of
brain, which does not seem to have been an important limiting factor
since the late Homo erectus. The increase in size of brain, called encephalisation,
targeted especially the cerebrum, the area of the brain dedicated to
sophisticated functions. Thus, encephalisation made possible complex
symbolic systems, but it is important to notice that encephalisation
reached a sufficient volume to support complex symbolic systems about
500,000 years ago with Homo heidelbergensis but the earliest complex
symbolic systems detected date about 230,000 years ago. >From that
moment AMHS appears 160,000 years ago in Africa and Neandertals appear
in Europe and Levant about 130,000 years ago, two species originated
perhaps by the same environmental factor, i.e. increased social relationships
in different regions. The Neandertals seem however to have continued
the path of expanding the size of the brain, perhaps hitting a physical
limit in doing so. On the contrary, AMHS keeps expanding its cerebral
capabilities as well, but the volume of the brain shrinks during this
process exactly at the time the symbolic behaviour becomes apparent.
What happened then to AMHS? In short, it may be that the cerebrum may have fully developed.
The cerebrum is the corrugated superficial area of the brain that hosts
the most complex cerebral functions and that today forms the largest
part of the brain. The corrugated structure of the cerebrum means that
it is a naturally compact tissue, which would have allowed the expansion
of the mass while density increased. Following this hypothesis, the
expansion of the mass should have been compensated for a while by the
increase in density. This process kept the brain size stable for long,
but eventually the cranial capacity may have been reduced temporarily
only to continue a slow expansion later. After all the evolutionary
trend that expanded the brain may have not stopped: challenged by the
dimensions necessary to support a "plain" brain capable of
the next level of intelligence, nature may have just adopted a more
functional form, expanding the cerebral faculties and reducing the physical
space necessary. Remarkably, the brain is today a dynamic organ capable
of small expansions and contractions within as little as three months
because of its management of density (Draganski et al 2004). This capability,
named neuroplasticity, may be the true innovation of AMHS and the one
responsible, after 120,000-150,000 years from the biological change,
of symbolic behaviour. To conclude, two possible hypotheses linking biological and archaeological
data have been presented. Both require much more than a single chromosomal
change. Moreover, to manifest their effect on the archaeological record
and behaviour the biological transformations needed about 250,000 years
for complex symbolic systems to appear and about 150,000 years for modern
human behaviour. Both biological changes were extreme enough to cause
speciation and the effect on the archaeological record is sudden and
extreme as well. The distance in time between biological events and
archaeological effects is such that more research and many debates will
certainly continue, but at least we have seen that it is possible to
link the two set of data. Conclusions This short and incomplete discussion of Stone Age archaeological
evidence finds its reason to be in the search of criteria capable of
correctly recognise symbolisms at the dawn of humanity. We have seen
that the key problems are in fact intertwined and not entirely within
the dominion of archaeology. Biology is as important as archaeology,
but both data sets are still fragmentary. On one side, the archaeological
record points clearly towards an early introduction of complex symbolic
systems, but these were not clearly associated to AMHS and modern symbolic
behaviour. The difficulty may have been surpassed if archaeological
data would not become apparently contradictory suggesting that symbolic
behaviour, as we know it, appeared not earlier than 40,000 years and
was associated specifically to AMHS. As a result, criteria of symbolicity
have been built from various perspectives, such as biological (e.g.
relationship AMHS - symbolism), archaeological (e.g. non-utilitarian
tools are symbolic), ethno-anthropological and philosophical. Integration
of datasets has always been the major weakness in this field of research. The methodological issues of identifying symbols cannot be separated
from the origins of symbols as instead Nowell (symposium papers: 12)
suggests referring particularly to the theoretical debates. If we cannot
agree on what complex symbolic systems and symbolic behaviour are, then
we cannot recognise them securely. In trying to recognise some phases
into the development of modern symbolic behaviour, we may be able to
recognise what symbolic behaviour is and what symbols are and begin
to formulate criteria capable to recognise fully modern symbolic behaviour
as well as any meaningful degrees of it. The archaeological evidence,
though fragmentary, demonstrates that throughout the Palaeolithic a
few specific symbols were part of the life of every individual, or it
would be impossible to have their repetition enormously distanced in
both geographical and spatial terms. Bouissac (symposium papers: 19)
points out that replication is indeed "the surest indicator"
of symbolic value. It would be pretentious to affirm that this brief review of evidence
has contributed to our understanding of biological and genetic processes
in the development of intelligence, cognition and symboling. However,
it has put forward the need of integrating various types of evidence
as ordinary methodological procedure. As we have seen, one piece of
evidence may explain another, easily crossing the boundaries of different
fields. In this work the archaeological perspective has been used as
primary source of evidence, at least because it is better known to the
writer, but biological evidence has been used to form a balanced picture
of the past research and to explain the archaeological record. It is likely that consciousness, the ability of abstract thought
and symbolism have originated early in human evolution and have been
refined ever since. Ultimately, if a change in human anatomy freed two
limbs and stimulated new advanced neurological functions that lead to
cognition, than it is possible that the creation of a social environment
in which cognition was stimulated produced a change in the brain that
allowed members of one species to proceed further on the evolutionary
process and supersede any other species. Questions about the relationship of Neandertals to our ancestors
and the origins of consciousness have received a timid answer here,
in spite of not having been asked or especially targeted. In brief,
Neandertals were probably biologically different from our ancestors
mainly in the structure of the brain. There is no physical proof of
this as only cranial capacity is available, but this finding seems to
fit with the overall archaic features of early Neandertals. Neandertals
were adapted to the European environment and appear to have very much
and it is unclear as yet what archaic feature may have been determinant
in their demise. Yet, their culture and behaviour do not seem to have
been archaic in anything up to the arrival of AMHS in Europe and their
almost immediate development of modern behaviour. For what concerns
consciousness, this feature should have appeared before any symbolic
system as it may have been the direct cause for their emergence. These
statements only call for further research and they are presented here
to provide a perspective as broad as possible of both questions and
prospects in this field of research. We will never be sure of which thoughts moved the individuals at
Qafzeh Cave to use specifically red ochre, but we may gain an understanding
of why they used red ochre (e.g. it was an item connected to abstraction)
and what, in general terms, they wanted to do with it (e.g. they wanted
to express certain meanings in a symbolic way). As soon modern symbolic
behaviour appears the complex symbolic systems change dramatically.
We may find difficult to argue about the similarities of the burial
at Paviland Cave and the Early Natufian burials, which are not and cannot
be product of the same culture, but they both originated from a common
cultural background unimaginably long (not less than 100,000 years).
The symbols used may been developed and employed for extremely long
periods, but it took as little as the transition from Early to Late
Natufian to see previous symbols disappear and new ones appear originating
both from the Palaeolithic culture (e.g. skull removal) or being formulated
within that culture (e.g. reburial of multiple crania as secondary activity
and symbolic absence of grave goods). Art is perhaps the first evidence of a cultural dynamism unknown
previously, but such dynamism can be explained in the same way for both
art and funerary contexts. The increase in social relationships meant
that symbols (and culture) could be passed to other individuals more
easily as well as new variants could be produced and spread in shorter
times. The relationship between social dynamics and symbolic meanings
is evident in the Natufian period, when the merging of different groups
has explosive effects on symbolic expression and can be guessed and
perhaps proven in the case of European Palaeolithic art, which spread
relatively quickly with constant motifs. The final result is that symbolic
expressivity mutated from material representation of abstract ideas
in a physical world to a proper language, understood by most and dynamic,
where symbolic materials are the words describing the metaphysical (i.e.
beyond the physical; abstract) world of the I/self-consciousness. Continuing
the metaphor of language, the structuring of words into sentences equals
in our case to the structuring of basic material symbols into rites. Thus, the recognition of basic words-symbols and their minimal structuring
give us an introspective into the Palaeolithic world, where simple criteria
such as the non-utilitarian one inform us of people capable of metaphysical
thinking. The recognition of "replication" or ritual activity
is determinant for modern symbolic behaviour to be recognised. Indeed,
the term "ritual" may substitute the overused and unclear
term "modern". Humans showing ritual (modern) symbolic behaviour
may have been psychologically more complex than other contemporary individuals
not showing this behaviour, no matter their species. However, we should
not forget that they were all humans capable of thinking beyond the
physical world and the immediate. In conclusion, not a single criterion used to identify symbolicity should be abandoned, no matter how weak its theoretical basis is. The five criteria suggested by Bouissac (symposium papers), the non-utilitarian criterion and any other are all appreciated. However, criteria of symbolicity need to be used as a set and never individually. Rituality is the watershed between archaic and modern symbolic behaviour, but rituality evidently did not appear overnight (especially if genetic changes had a role) and therefore the overall complexity must be assessed taking in consideration various criteria. A methodology capable of consider the whole range of evidence is important and therefore archaeology, cognitive sciences and biology should be used together. Also, very long periods and large areas should be considered unitarily because the recognition of symbols throughout Stone Age offers the possibility of finding repetitive patterns back and forth. Thus, not generic repetition but rituality should be placed as watershed criterion between archaic symbolic behaviours involving a few "complex symbolic systems" on their own and modern symbolic behaviours using symbols as words and rites as structured sentences. In this view, rituality may be defined as a form of language by means of symbols, i.e. a powerful communication tool capable to express abstract ideas in the physicality of the material world. In this way, because the materiality can be perceived through the senses by any individual in a very similar manner, rituality as a language can always be understood to some degree, capable as it is of circumventing any cultural, geographical and chronological barrier which limits verbal communication.
Aldhouse-Green, S. 2000. Paviland Cave and the 'Red Lady': a definitive report, Western Academic & Specialist Press, Bristol. Barham, L. S. and Smart, P. 1996. 'Early date for the Middle Stone Age of central Zambia', Journal of Human Evolution, no. 30, pp. 287-290. Barham, L. S. 1998. 'Possible early pigment use in South-Central Africa', Current Anthropology, no. 39, pp. 703-710. Belfer-Cohen, A. 1995. 'Rethinking Social Stratification in the Natufian Culture: The Evidence from Burials', Oxbow Monograph, pp. 9-16. Conard, N. J. 2003. 'Palaeolithic ivory sculptures from southwestern Germany and the origins of figurative art', Nature, no. 426, pp. 830-832. Davidson, I. and Noble, W. 1993. 'Tools and language in human evolution', in Tools, language, and cognition in human evolution, eds. Gibson, K. and Ingold, T., Cambridge University Press, Cambridge, pp. 363-388. Draganski, B., Gaser, C., Busch, V., Schuierer, G., Bogdahn, U. and May, A. 2004. 'Changes in grey matter induced by training', Nature, no. 427, pp. 311-312. Gould, S. J. and Eldredge, N. 1977. 'Punctuated equilibria: the tempo and mode of evolution reconsidered', Paleobiology, no. 3, pp. 115-151. Henneberg, M. 1998. 'Evolution of the human brain: Is bigger better?' Clinical and Experimental Pharmacology and Physiology, vol. 25, no. 9, pp. 745-749. Henshilwood, C. S. and Marean, C. W. 2003. 'The Origin of Modern Human Behavior: Critique of the Models and Their Test Implications', Current Anthropology, vol. 44, no. 5, pp. 627-652. Hovers, E., Ilani, S., Bar-Yosef, O. and Vandermeersch, B. 2003. 'An Early Case of Color Symbolism: Ochre Use by Modern Humans in Qafzeh Cave', Current Anthropology, vol. 44, no. 4, pp. 491-522. Knight, C., Power, C. and Watts, I. 1995. 'The human symbolic revolution: A Darwinian account', Cambridge Archaeological Journal, no. 5, pp. 75-114. Kuijt, I. 1996. 'Negotiating Equality through Ritual: A Consideration of Late Natufian and Prepottery Neolithic A Period Mortuary Practices', Journal of Anthropological Archaeology, vol. 15, no. 4, pp. 313-336. McBrearty, S. and Brooks, A. S. 2000. 'The revolution that wasn't: a new interpretation of the origin of modern human behavior', Journal of Human Evolution, vol. 39, no. 5, pp. 453-563. Neuville, R. 1951. Le Paléolithique et le mésolithique du désert de Judée, Paris. Pettitt, P. 2002. 'The Neanderthal dead: exploring mortuary variability in Middle Palaeolithic Eurasia', Before Farming, no. 1 (4), pp. 1-19. Power, C. and Aiello, L. C. 1997. 'Female proto-symbolic strategies', in Women in human evolution, ed. Hager, L. D., Routledge, London and New York, pp. 153-171. Schwarcz, H., Buhay, W. M., Grün, R., Valladas, H., Tchernov, E., Bar-Yosef, O. and Vandermeersch, B. 1989. 'ESR dating of the Neanderthal site, Kebara Cave, Israel', Journal of Archaeological Science, no. 16, pp. 653-661. Sinclair, A. 2003. 'Art of the ancients', Nature, no. 426, pp. 774-775. Valladas, H., Mercier, N., Joron, J.-L. and Reyss, J.-L. 1998. 'GIF laboratory dates for Middle Palaeolithic Levant', in Neanderthals and Modern Humans in Western Asia, eds. Akazawa, T., Aoki, K. and Bar-Yosef, O., Plenum, New York, pp. 69-75. Valladas, H., Clottes, J., Geneste, J. M., Garcia, M. A., Arnold, M., Cachier, H. and Tisnerat-Laborde, N. 2001. 'Palaeolithic paintings: Evolution of prehistoric cave art', Nature, no. 6855, p. 479. Weinstein-Evron, M. 1993. 'The Natufian Use of el-Wad Cave, Mount Carmel, Israel', in The human use of caves, eds. Bonsall, C. and Tolan-Smith, C., Archaeopress, Newcastle upon Tyne, pp. 155-166. White, T. D., Clark, J. D., Beyene, Y., Woldegabriel, G., Hart,
W. K., Renne, P. R., Gilbert, H., Defleur, A., Suwa, G., Katoh, S.,
Ludwig, K. R., Boisserie, J.-R. & Asfaw, B. 2003. 'Stratigraphic,
chronological, and behavioural contexts of a Pleistocene Homo sapiens
from Middle Awash, Ethiopia', Nature, no. 423, p. 742-747. |
Information: Paul
Bouissac  
|
Design by: H. Harris
|
Copyright ©2003. All rights
reserved
|