| Sarah Howell-Meurs (University
of Melbourne, Australia)
showell_meurs@hotmail.com
Eastern Anatolia is characterised by a
climatic and topographic dichotomy dictated
by the presence of the Anatolian plateau
and highlands to the north and semi-arid
lowlands to the south. Early Bronze Age
settlement patterns and architectural evidence
broadly support this notion of a dichotomy,
with the northern provinces such as Bayburt
and Erzurum being characterised by low-density
occupation consisting of small villages,
in contrast to a tendency toward higher-density
occupation which included medium- and large-sized
towns and administrative centres characteristic
of the southeastern provinces of Urfa and
Malatya (Yakar 1985). While obvious contrasts
in the exploitation strategies employed
at upland and lowland sites have been noted
for early pastoral economies of south eastern
Europe (Greenfield 1991), little research
examines whether altitude and consequently
topography and climate exerted a significant
impact over the economic systems of eastern
Anatolia. Given the complex interrelationship
between settlement, environment and subsistence,
an examination of the economic strategies
employed at upland and lowland sites throughout
eastern Anatolia highlights the extent to
which topographical and climatic factors
influenced economic patterns. While the
reconstruction of animal resource exploitation
patterns through the analysis of faunal
remains has been relatively intense in the
southeast, evidence has until lately been
entirely lacking from the northeastern regions.
Recent analysis of the faunal assemblages
from the northeastern Anatolian site of
Sos Höyük and Büyüktepe Höyük (Howell-Meurs
1998), however, permits an examination of
the effects of topography and climate over
animal resource use in the upland compared
with the lowland sites of eastern Anatolia
during the Early Bronze Age period.
Investigation
and comparison of the economic and animal
resource-use patterns of upland and lowland
sites in eastern Anatolia is hampered by
a poor representation of sites, and a lack
of published analyses of faunal remains
from excavated sites. Of those sites with
detailed data relating to pastoral production
and exploitation of wild animals, many are
characterised by small assemblage size or
a lack of correlation and thus comparability
between the analytical methods chosen to
investigate assemblage characteristics.
The sites used in the current analysis were
chosen on the basis of the accessibility
of detailed data and use of generally comparable
methods of assemblage analysis in the reports.
Sos Höyük and Büyüktepe Höyük are located
in the provinces of Erzurum and Gümüşhane,
and lie within the Anatolian plateau at
altitudes of approximately 1800m and 1500m
above sea level respectively. These sites
comprised small villages in the Early Bronze
period. The lowland sites considered in
the current study, Hassek Höyük (Stahl 1989)
and Lidar Höyük (Kussinger 1988), and Gritille
(Stein 1988), located in the Urfa and Adiyaman
provinces respectively, are all located
in the Karababa Basin at an altitude of
approximately 400m above sea level. Greater
diversity in site function is apparent amongst
these lowland sites with Hassek Höyük functioning
as a large urban centre, Lidar Höyük as
an administrative district centre, and Gritille
as a small-scale village settlement (Yakar
1985, Stein 1988). A further site, Korucutepe
(Boessneck and von den Driesch 1975), located
on the Altinova plain in the Elazig province
at approximately 800m above sea level, is
intermediate in altitude between those of
the upland and lowland sites and comprised
a large urban centre. This site was examined
to investigate whether it displayed pronounced
pastoral and economic affinities with the
economies of either upland and lowland environments.
All
of the sites considered in the current study
are situated on plains bordered by mountain
ranges, although the climate and surrounding
vegetation are markedly different between
the upland and lowland sites. The high-altitude
sites are subject to a continental climate
and dominant summer drought system, with
low annual precipitation of approximately
400mm per year, short summers and extremely
long and harsh winters with daily maximum
temperatures in January consistently below
-15oC (Alex 1985a, 1985b, Alex
1983). This is in contrast to the semi-arid
climate of the Karababa Basin in which the
annual precipitation of 400-600mm is concentrated
during winter, and average temperatures
reach between 0-5oC in winter
and 30-35oC in summer (Stein
1988). The climate in the Altinova Plain
is intermediate between the upland and lowland
regions, consisting of a summer drought
with an annual precipitation of 400mm, and
average summer and winter temperatures of
approximately 19 oC and 7
oC respectively (Alex 1985c:105).
In terms of vegetation, the regions surrounding
Sos Höyük and Büyüktepe Höyük are characterised
by steppe. By contrast, the sites in the
Karababa Basin, located at the junction
between the Anatolian highlands and North
Syrian plain, exhibit three vegetation types,
being mixed broad-leaved and needle-leaved
woodland, Irano-Turanian steppe and desert
vegetation (Stein 1988). The region surrounding
Korucutepe is characterised by natural vegetation
of broad-leaved and needle-leaved woodland
(Zeist and Bottema 1991). The vastly differing
climatic and topographical environments
of the upland and lowland sites might be
expected to impose significant constraints
over the activities of the inhabiting human
populations and by extension their systems
of pastoral production.
The
relative representation of wild to domestic
taxa within each assemblage was examined
to determine if any differences were apparent
between the exploitation patterns of highland
and lowland sites (Figure 1).
Figure
1. The relative abundance of wild to domestic
taxa in terms of NISP for Sos Hoyuk (N=2477),
Buyuptepe (N=34), Korucutepe (N=866), Lidar
Hoyuk (N=2989), Hassek Hoyuk (N=12962) and
Gritille (N=1205).
Examination
of the results reveals a consistently low-level
exploitation of wild resources, with all
assemblages providing clear evidence of
an overwhelming emphasis on domestic taxa
for subsistence needs. Further, the pattern
of wild animal use appears to be consistent
across assemblages, with a relatively broad
suite of species each contributing relatively
few specimens (Howell-Meurs 1998, Kussinger
1999, Stahl 1989, Stein 1988). Some exception
to this is provided by the assemblage from
Korucutepe, in which the hunting of red
deer figures more prominently than is apparent
elsewhere, suggesting a greater abundance
and proximity of woodlands to this site
(Boessneck and von den Driesch 1975 124).
The likelihood of detecting rare taxa in
an assemblage increases with, and is thus
dependent on sample size. It is therefore
possible that a number of the Early Bronze
Age assemblages may reflect an under-representation
of wild relative to domestic taxa. Despite
this, an increase in the representation
of wild taxa for the smaller-sized assemblages
would not alter the fact that exploitation
of wild resources between upland and lowland
sites was reasonably consistent. The low
level of exploitation of wild resources
may have resulted from a variety of factors
that were consistent throughout differing
altitudes in eastern Anatolia during the
Early Bronze Age. These may have included
a reduction in the proximity of habitat
suitable for some wild species through processes
including increased agricultural intensification
involving land clearance, and deforestation
for wood resources for building and fuel,
with the result that many wild taxa were
confined to more remote and perhaps inaccessible
environments. Similarly the continued emphasis
upon pastoralism evidenced in these assemblages
may have provided neither the labour nor
the impetus for the large scale exploitation
of wild resources.
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Trends in the abundance of the main domesticates
for each assemblage may provide insights into
altitudinal differences in the focus of pastoral
strategies (Figure 2). Figure
2. The relative abundance of the main domesticates
in terms of NISP for Sos Hoyuk (N=2362),
Buyuptepe (N=29), Korucutepe (N=721), Lidar
Hoyuk (N=2791), Hassek Hoyuk (N=12709) and
Gritille (N=1133).
With
the exception of Hassek Höyük, sheep and
goats emerge as the most abundant taxa in
each assemblage. Although this predominance
varies significantly from between 52% to
69%, it does not appear to be correlated
to site altitude. Sos Höyük and Büyüktepe
Höyük reflect a similar abundance of ovicaprids
to Korucutepe and the lowland sites. The
favouring of ovicaprids as the principal
herded domesticate at both upland and lowland
sites may have occurred for two reasons:
these taxa are able to adapt to a wide diversity
of habitats and furnish multiple products.
The suitability of ovicaprids to marginal
environments including steep and mountainous
terrain and their ability to graze very
low vegetation, allows for the utilisation
of the hilly lands adjacent to the plains
in which each of the sites is located. As
neither cattle nor pigs can effectively
utilise these regions, the keeping of ovicaprids
allows for the exploitation of what would
be an otherwise under-utilized resource.
Sheep and goats may also yield a variety
of products including milk, wool, hair,
meat, hides and horn. An emphasis on the
herding of ovicaprids could therefore provide
a wide array of returns. These features
may have made ovicaprids equally desirable
and versatile as stock for both upland and
lowland pastoralists.
Sites
from the lowland semi-arid ecosystems, however,
show a consistently lower abundance of cattle,
relative to sheep and goats, than is apparent
at the upland sites. Korucutepe appears
to indicate an intermediate level of cattle
abundance, although tending more toward
the lesser relative representation apparent
at the lowland sites. The lower representation
of cattle within the lowland environments
accords well with the fact that cattle have
a lower tolerance for semi-arid conditions
(Spooner 1973:8), and thus will tend to
occupy a less significant role in the subsistence
strategies of herders occupying such areas.
This is in part owing to the high water
requirements of domestic cattle, which increase
significantly with higher ambient temperatures
(Wells 1970:122). The higher altitude and
lower temperatures of the highlands surrounding
both Sos Höyük and Büyüktepe Höyük may have
thus favoured the herding of a greater proportion
of cattle than at sites in the lowland,
semi-arid environments. Cattle in addition
require substantial quantities of forage
and pasture. The location of both the upland
and lowland sites on plains adjacent to
mountain ranges would however have limited
the grazing land available for cattle, as
the species is best suited to flat ground
or land with only low undulations. The subsequent
confinement of this species principally
to the plains would have resulted in it
being in direct competition with arable
lands. The lesser relative abundance of
cattle at lowland sites may therefore indicate
the lesser availability of land for cattle
to graze through a more extensive use of
plains for agriculture perhaps coupled with
the apparently higher levels of settlement
density in these regions.
With
pig abundance ranging from between one to
twenty percent within the majority of Early
Bronze Age assemblages, a clear neglect
of this species as a major food source is
evident, irrespective of altitude. The relatively
low representation of pigs is however a
trend apparent throughout the Near East
for many millennia following their initial
domestication (Zeder 1996:298). The consistently
low representation in the upland and lowland
sites suggests significant pressures discouraging
the widespread large scale herding of pigs
during the Early Bronze Age period. Pigs
require shelter, typically in the form of
vegetation, from both sun and extremes of
weather and also need a reliable water source
close by, soft ground and, in harsh sun,
mud wallows. With a dietary preference for
acorns and beech-mast, their ideal habitat
comprises moist, open woodland (Diener and
Robkin 1978, Grigson 1982:300). Pigs have,
in addition, much higher water requirements
than do the other main domesticates, with
daily watering of three parts water to one
part feed necessary. Even higher levels
are required by pregnant sows (Zeder 1996,
301). Their low abundance within most assemblages
suggests that these sites were lacking in
one or more of these characteristics. As
all sites were located adjacent to perennial
water sources, the low abundance of pigs
may be related to a lack of settlement proximity
to woodland and vegetation cover as a source
of food and shelter, a conclusion also suggested
by the low representation of wild resources
at each site. A clear exception to this
pattern is provided by the assemblage from
Hassek Höyük, in which pigs comprised over
50% of the main domesticate bones identified.
The proximity and environmental comparability
of this site to the other lowland sites
analysed suggests that cultural rather than
ecological factors may be dictating the
nature of pig exploitation.
The
nature of pastoral strategies can most readily
be investigated through analysis of the
age and sex data relating to the main domesticates.
Patterns of eruption and attrition on the
mandibular remains in addition to the state
of epiphyseal fusion of the long bones all
provide indicators of mortality. Sexual
dimorphism in the size and morphology of
various skeletal elements including the
metapodials, horn cores and pelvis may permit
for differentiation between male and female
specimens. This allows for the reconstruction
of survivability profiles for the herd in
which peaks in mortality of different age
classes and between males and females can
be highlighted and interpreted with reference
to models of idealised herd management for
specific products such as milk, wool, traction
or meat (Payne 1973, Higham and Message
1970). The analysis was hampered, however,
by a lack of data or poor sample size. As
a results, herd management regimes could
only be investigated for the ovicaprid and
cattle remains from a selection of sites.
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Mortality profiles for the ovicaprid assemblages
from upland and lowland Early Bronze Age sites
appear to be comparable in form (Figure 3).
Figure
3. Survivorship curve for the ovicaprid
remains for Sos Hoyuk (N=58), Korucutepe
(N=16), Lidar Hoyuk (N=53), Hassek Hoyuk
(N=90) and Gritille (N=32).
In
each case, juvenile mortality is poorly
represented, while the highest mortality
is apparent amongst the subadult age classes.
Although lacking for the other assemblages,
epiphyseal fusion data from Sos Höyük and
Gritille support the profiles suggested
by the dental remains (Table 1). With the
exception of Gritille, the assemblages each
indicated a predominance of adult females
(Boessneck and von den Driesch 1975:68,
Howell-Meurs 1998:113, Kussinger 1988:59,
Stahl 1989:72, Stein 1988:188). With high
subadult mortality and a predominance of
adult females, these profiles conform most
readily to a meat production strategy (Payne
1973), although this may have been supplemented
by the exploitation of secondary products
from adult breeding stock. The assemblage
from Korucutepe, with a later peak in mortality
at two to four years, provided the only
evidence of a divergence from the mortality
patterns apparent for the other Early Bronze
Age assemblages, reflecting a greater emphasis
on wool production (Boessneck and von den
Driesch 1975 38).
| Age |
|
SOS |
GRT |
| Months |
Element |
fused |
unfused |
fused |
unfused |
| 8-10 |
scapula |
44 |
1 |
11 |
3 |
| |
os coxae |
13 |
4 |
- |
- |
| |
p. radius |
34 |
2 |
8 |
0 |
| |
d. humerus |
31 |
4 |
12 |
3 |
| Total |
|
122 |
11 |
31 |
6 |
| 12-24 |
p. phalanx 1 |
29 |
9 |
1 |
0 |
| |
p. phalanx 2 |
11 |
1 |
2 |
0 |
| |
d tibia |
30 |
10 |
14 |
2 |
| |
d metapodials |
32 |
23 |
14 |
5 |
| Total |
|
102 |
43 |
31 |
7 |
| 30-36 |
p ulna |
4 |
3 |
0 |
3 |
| |
p femur |
6 |
14 |
5 |
2 |
| |
calcaneus |
12 |
3 |
2 |
0 |
| Total |
|
22 |
20 |
7 |
5 |
| 36-48 |
d humerus |
0 |
5 |
1 |
2 |
| |
p tibia |
3 |
5 |
0 |
3 |
| |
d radius |
6 |
13 |
1 |
1 |
| |
d femur |
3 |
6 |
1 |
1 |
| Total |
|
9 |
29 |
3 |
7 |
Table
1. Epiphyseal fusion data for ovicaprid
remains from Sos Huyuk and Gritelle
Evidence
for the construction of survivability profiles
for the cattle remains from Early Bronze
Age sites is generally lacking. Only three
assemblages, Sos Höyük, Lidar Höyük and
Hassek Höyük, allow for the determination
of survivability curves based upon mandibular
eruption and attrition. The resulting profiles
suggest extremely low mortality amongst
juveniles and subadults prior to two and
a half years (Figure 4).
Figure
4. Survivorship curve for the cattle remains
for Sos Huyuk (N=25), Lidar Hoyuk (N=20)
and Hassek Hoyuk (N=21).
Epiphyseal
fusion data from Sos Höyük suggests a peak
in mortality between two and a half and
four years, although the majority of animals
nevertheless survived beyond four years
into full adulthood (Table 2). Females outnumber
males amongst the adults within each of
these assemblages (Howell-Meurs 1998:86,
Kussinger 1988:21, Stahl 1989:22). These
results suggest a mixed strategy in which
some males were culled for meat prior to
four years, with the remainder retained
for traction work, while adult females provided
milk resources and served as breeding stock
(Stahl 1989:15, Kussinger 1988:19). Epiphyseal
fusion data from Gritille contrasts somewhat
with the dental data from Sos Höyük, Lidar
Höyük and Hassek Höyük, with a pronounced
peak in mortality apparent prior to four
years, suggesting a strategy more specifically
geared toward meat production (Stein 1988:222).
The lack of dental data and specimens identified
to gender within this assemblage precluded
further investigation of this trend. Skeletal-part
representation analysis within each assemblage
again indicates the presence of entire carcasses
at the settlements suggesting local production
and consumption rather than exchange in
each case.
|
Age (Months) |
Element |
fused |
unfused |
| 7-10 |
os coxae |
16 |
0 |
| Total |
|
16 |
0 |
| 12-20 |
p. phalanx 1 |
41 |
1 |
|
|
p. phalanx 2 |
34 |
1 |
|
|
p radius |
25 |
0 |
|
|
d humerus |
25 |
3 |
| Total |
|
125 |
5 |
| 24-30 |
d tibia |
15 |
3 |
|
|
d metapodials |
27 |
2 |
| Total |
|
42 |
5 |
| 42-48 |
p humerus |
4 |
1 |
|
|
p femur |
9 |
3 |
|
|
p tibia |
1 |
3 |
| |
d radius
|
7 |
2 |
| |
d femur
|
3 |
2 |
| Total
|
|
24 |
11 |
Table 2. Epiphyseal fusion data for cattle
remains from Sos Hoyuk.
In contrast to Greenfields findings for
the eastern Balkans, in which pronounced
differences in economic strategies were
apparent between upland and lowland sites,
the herding strategies and animal use patterns
apparent for the eastern Anatolian sites
examined here appear to be reasonably consistent.
The ovicaprid and cattle mortality data
and relative representation of wild to domestic
taxa indicate little variation in the nature
of animal production strategies and use
of wild resources between upland and lowland
sites, suggesting that these factors were
not largely dependent on site altitude or
environment. Some variation was apparent
however between upland and lowland sites
in terms of relative species abundance of
the main domestic taxa and this could be
correlated to some extent with climate and
topography and thus altitude. Broadly, though,
trends were comparable across the assemblages
analysed, irrespective of site altitude.
While animal use patterns do not appear
to correlate obviously with site altitude,
various differences in exploitation strategies
such as the apparent focus on wool resources
at Korucutepe may in part be related to
site function. Ethnographic analogues, for
instance, imply that smaller-scale settlements
such as those represented at Sos Höyük,
Büyüktepe Höyük and Gritille may have been
able to meet their wool and milk requirements
without structuring herd productivity exclusively
toward these goals (Redding 1981:48). Twentieth-century
Lur nomads, who raise flocks of ovicaprids
primarily for subsistence, with fibre constituting
a by-product, obtain enough wool and goat
hair from their stock to supply their own
needs plus furnish a surplus that is sold
either to itinerant dealers or in the local
townships (Mortensen 1993:279). Similarly,
Black-Michaud (1986:43) provides an account
of the regime undertaken by Lur nomads to
permit simultaneous use of sheep milk resources
by offspring and humans including the restriction
of suckling time and milking prior to suckling.
The wool profile apparent at the large urban
centre of Early Bronze Age Korucutepe may
therefore indicate larger scale production
for local consumption and perhaps to create
a surplus for exchange. Why this pattern
was apparent at Korucutepe but not at the
comparably-sized settlements of Hassek Höyük
and Lidar Höyük requires further investigation.
The small number of sites examined and
lack of detailed data for various aspects
of the analysed assemblages significantly
limited the current investigation. Future
analyses of assemblages, particularly from
highland contexts, and the availability
of detailed data from a wider geographic
range of upland and lowland habitats would
serve to clarify significantly the influence
of altitude over economic strategies and
allow for assessment of the pervasiveness
of the trends detected in the current study.
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