Professional Documents
Culture Documents
ABSTRACT
Numerous Bronze Age cemeteries in the
oases surrounding the Taklamakan Desert of the Tarim
Basin in the Xinjiang Uyghur Autonomous Region, western China, have yielded both mummied and skeletal
human remains. A dearth of local antecedents, coupled
with woolen textiles and the apparent Western physical
appearance of the population, raised questions as to where
these people came from. Two hypotheses have been offered
by archaeologists to account for the origins of Bronze Age
populations of the Tarim Basin. These are the steppe
hypothesis and the Bactrian oasis hypothesis. Eight
craniometric variables from 25 Aeneolithic and Bronze
Age samples, comprising 1,353 adults from the Tarim
Basin, the Russo-Kazakh steppe, southern China, Central
Asia, Iran, and the Indus Valley, are compared to test
which, if either, of these hypotheses are supported by the
pattern of phenetic afnities possessed by Bronze Age
inhabitants of the Tarim Basin. Craniometric differences
between samples are compared with Mahalanobis gener-
200
INHABITANTS OF XINJIANG
201
Fig. 1. Geographic location of craniometric samples. Sample abbreviations from Table 1. Xinjiang samples (QAW, ALW, and KRO)
and Chinese sample from Hainan (HAI) are represented by asterisks; North Bactrian samples, by stars; Iranian samples, by
pentagons; Turkmenian, Caucasus, and Tajik samples, by triangles; Indus Valley samples, by circles; and Russo-Kazakh samples, by
squares.
Indo-Iranian (which is well-represented by a number of languages in the Tarim Basin) or any other
eastern (satem) Indo-European languages (other
than loan words). Within the phylogeny of the IndoEuropean languages, Tocharian languages are either placed with the western (centum) languages
of Europe (Adams, 1984; Hamp, 1998), or are regarded as languages that split from the rest of the
Indo-European languages at such an early date that
they lack many of the isoglosses found between
other Indo-European languages (Ringe et al., 1998).
Mallory and Mair (2000, p. 240 246) suggested that
the separation of Tocharian speakers from other
Indo-European-speaking communities may have occurred as early as the fourth millennium B.C., and
they identied the Afanasievo culture (ca. 3500
2500 B.C.), a primarily pastoralist culture found in
the Altai and Minusinsk regions of the Eurasian
steppe, as a possible source for a Tocharian presence
in the Tarim Basin (Mallory, 1989, p. 62, 263, 1995,
202
liest Bronze Age sites in Xinjiang, such as Qawrighul (Kuzmina, 1994, p. 241, 1998, p. 69; Mallory,
1995; Mallory and Mair, 2000).
The Afanasievo culture itself is believed intrusive
to the eastern steppe and is held to share the closest
similarities to the Yamnaya culture (3500 3000
B.C.; Mallory and Mair, 2000) found in the PonticCaspian region of the Russian steppe (Alexeev,
1961; Anthony, 1998, p. 104; Chernykh, 1992;
Gryaznov and Vadezkaya, 1968; Kuzmina, 1998;
Mallory, 1989, p. 62, 1995, 1998, p. 189; Mallory and
Mair, 2000; Parpola, 1998; Posrednikov, 1992; but
see Shishlina and Hiebert, 1998, p. 222223). As
noted by Mallory (1995) and Mallory and Mair
(2000, p. 381382), an eastward emigration and subsequent isolation of Yamnaya-derived Afanasievo
populations in the eastern steppe provides a possible
explanation for the appearance of Tocharian in the
Tarim Basin of Xinjiang. Hence, the apparent similarities between Tocharian and such western IndoEuropean languages as Celtic and Italian are due to
a common retention of proto-Indo-European archaicisms (Mallory, 1989, p. 61), while the differences
between Tocharian and neighboring Indo-Iranian
might be explained by the peripheral position of
proto-Tocharian populations with respect to the
emergence of Indo-Iranian languages. This assertion appeared to be supported by Hans (1998) contrast of cranial and facial indices which indicated
that the earliest individuals from Qawrighul (type I
tombs; see below) were most similar to individuals
from Afanasievo cultural contexts (see Mallory and
Mair, 2000, p. 240 243).
Many proponents of the steppe hypothesis contend that the immigration of Afanasievo populations
to the Tarim Basin was followed by a later inux of
populations derived from the Late Bronze Age Andronovo culture complex (ca. 2100 900 B.C.; Mallory and Mair, 2000) found to the west, northwest,
and north in the Pamirs, the Ferghana Valley, Kazakhstan, and the Minusinsk/Altai region (Chen
and Hiebert, 1995; Kuzmina, 1998; Mei and Shell,
1998; Parpola, 1998). As with earlier Afanasievo
populations, those accompanied by artifacts assigned to the Andronovo culture are believed to have
originated in the western Russian steppe. In this
latter case, ultimate stylistic origins of the artifacts
are traced to the Sintashta culture (ca. 2300 1900
B.C.; Mallory and Mair, 2000) of the southeast Urals
(Anthony, 1998; Anthony and Vinogradov, 1995, p.
36; Kuzmina, 1994; Mallory, 1998). The eastward
expansion of these likely Indo-Iranian-speaking peoples was facilitated by the development of the war
chariot (Anthony, 1998, p. 94; Di Cosmo, 1996, p.
90 91; Mallory, 1989; Parpola, 1998) and is reected by the rapid appearance of such regional
variants of the Andronovo culture designated as
Alakul, Federovo, Tazabagyab, Beshkent, and Vakhsh (Gupta, 1979; Hiebert, 1994; Kohl, 1984, p.
183184; Kuzmina, 1994; Masson, 1992b, p. 350
351; Sulimirski, 1970, p. 261, 263; Zdanovich, 1988).
203
INHABITANTS OF XINJIANG
The initial appearance of Andronovo-derived populations in the Tarim Basin is held to be signaled by
the introduction of new clothing styles, ceramic
wares, and burial customs as well as objects of tin
bronze, and objects associated with horses around
1200 B.C. (Barber, 1999; Kuzmina, 1998, p. 73; Mei,
2000, p. 7275; Mei and Shell, 1998).
The second model for the origin of the Bronze Age
inhabitants of Xinjiang is the Bactrian oasis hypothesis. Proponents of this model assert that settlement
of this region of western China came not from nomadic pastoralists of the steppe, but from sedentary,
agriculturally based populations of the Oxus civilization (the Bactrian-Margiana archaeological complex (BMAC); Hiebert, 1994) found west of Xinjiang
in Uzbekistan (north Bactria), Afghanistan (south
Bactria), and Turkmenistan (Margiana) (Barber,
1999; Chen and Hiebert, 1995, p. 287). Proponents of
this model emphasize the environmental similarities between the desert basins of eastern (Xinjiang)
and western Central Asia (Bactria, Margiana) and
maintain that the sophisticated irrigation techniques developed in the oases of Margiana and Bactria permitted the colonization of the river deltas
and oases surrounding the north, east, and southern
margins of the Taklamakan Desert (Barber, 1999;
Chen and Hiebert, 1995).
Barber (1999) suggested that the archaeological
record provides better evidence that the initial colonizers of the Tarim Basin were agriculturalists
from Bactria than nomadic pastoralists from the
Russian steppe. This evidence not only includes irrigation systems, evidence of western cultigens such
as wheat, and bones of sheep and goats, but also
evidence of carefully bundled bags containing Ephedra sp. found accompanying many Bronze Age Xinjiang burials. Use of ephedra is well-known in Oxus
civilization urban centers, where Hiebert (1994) and
Sarianidi (1987, 1990, 1993a,b, 1994; see also
Kussov, 1993; Meyer-Melikyan, 1998; Meyer-Melikyan and Avetov, 1998) found evidence of specialized areas known as white rooms where it is believed a ritual drink, known as haoma in Iranian
and soma in Indic, was consumed (but see Nyberg,
1995, p. 400; Parpola, 1995, p. 371). Ephedra does
not grow on the Russo-Kazakh steppe, nor is it associated with either Afanasievo or Andronovo cultures (Barber, 1999, p. 165; but see Parpola, 1998, p.
126 127).
Barber (1999) suggested that the Bronze Age settlement of the Tarim Basin was a two-step process
in which initial immigration came from the oases of
Bactria and Margiana, and is represented by remains found at such southeastern sites as Qawrighul. This was followed by a second wave of immigration soon after 1200 B.C. This time, immigrants
came from Andronovo populations located to the
northwest, and participants in this wave of immigration may be associated with the remains found at
northern Tarim Basin sites such as Alwighul, Hami,
Turfan, and Kucha. Barber (1999) claimed that ev-
204
205
INHABITANTS OF XINJIANG
TABLE 1. Samples considered in study
Maximum sample
size
Males
Females
ADM
AFA
AFM
AND
ALT
Code
22
17
18
25
40
11
7
11
31
42
Andronovo/Minusinsk
Afanasievo/Altai
Afanasievo/Minusinsk
Andronovo/Kazakhstan
Altyn depe/Turkmenistan
Site/region
Period
2100900 B.C.
35002500 B.C.
35002500 B.C.
2100900 B.C.
25002200 B.C.
ALW
CEMH
DJR
GKS
33
10
17
38
25
18
33
32
Alwighul/Xinjiang, China
Harappa/Indus Valley
Djarkutan/North Bactria
Geoksyur/Turkmenistan
650200 B.C.
19001600 B.C.
20001800 B.C.
35003000 B.C.
HAI
HAR
45
23
38
41
Hainan/South China
Harappa/Indus Valley
Living
Mature Harappan
Living
25002000 B.C.
KAM
KAR
133
14
118
13
Karasuk/Minusinsk
Kara depe/Turkmenistan
35003000 B.C.
KOK
KRO
KUZ
KUZ
MOL
QAW
SAMB
SAP
SHS
14
4
13
13
18
11
14
13
45
10
2
14
14
28
7
13
28
43
Kokcha III/Turkmenistan
Kroran/Xinjiang, China
Djarkutan/North Bactria
Djarkutan/North Bactria
Djarkutan/North Bactria
Qawrighul/Xinjiang, China
Samtavro/Caucasus
Sapalli tepe/North Bactria
Shahr-i Sokhta/Eastern Iran
18001500 B.C.
202 B.C.A.D. 150
18001650 B.C.
18001650 B.C.
16501500 B.C.
1800 B.C.
1400800 B.C.
22002000 B.C.
30002200 B.C.
TH2
TH3
TMG
9
102
9
7
36
11
33002500 B.C.
25001700 B.C.
1400800 B.C.
TMM
26
21
Tigrovaja-Makoni Mor/
Tajikistan
Tepe Hissar II
Tepe Hissar III
Late Bronze/Early
Iron Age
Molali phase
Alexeev (1961)
Alexeev (1961)
Alexeev (1961)
Alekseev (1967)
Kiiatkina (1967);
Hemphill (1999)
Han (1998)
Gupta et al. (1962)
Hemphill (1998)
Kiiatkina (1987);
Hemphill (1999)
Howells (1989)
Gupta et al. (1962);
Hemphill et al. (1991)
Rykusina (1976)
Ginzberg and Tromova
(1972)
Tromova (1961)
Han (1998)
Hemphill (1998)
Hemphill (1998)
Hemphill (1998)
Han (1998)
Abduselisvili (1954)
Hemphill (1998)
Pardini and SarvariNegahban (1976)
Pardini (1977, 1979
1980)
Krogman (1940)
Krogman (1940)
Bernhard (1967)
16501500 B.C.
Kiiatkina (1976)
Dates
Reference
206
1
8
48
55
54
52
51
45
not be assessed for published measurements for individuals recovered from Shahr-i Sokhta, Timargarha, or Hainan (southern China).
Methods
The covariance matrix for each sample was obtained
for males and females pooled together with listwise
deletion. Although pairwise deletion permits greater
effective sample sizes within each sample, listwise deletion was used to avoid systematic biases caused by
overrepresentation and underrepresentation of individual variables (Wilkinson, 1990). A pooled covariance matrix was obtained for all samples for which
individual data were available and bias-adjusted to
accommodate differences in sample size. Hence, those
samples represented by group-level data only (Andronovo-Minusinsk (ADM), Afanasievo-Altai (AFA),
Afanasievo-Minusinsk (AFM), Andonovo-Kazakhstan
(AND), Karasuk-Minusinsk (KAM), Kara depe (KAR),
Kokcha III (KOK), Samtavro (SAMB), and Tigrovaja
Balka-Makoni Mor (TMM)) were not used to construct
the pooled covariance matrix. Variable averages were
calculated for both males and females. Sex-standardized group values for each variable were obtained by
taking the average of male and female mean values for
each sample (Table 3). The bias-adjusted pooled covariance matrix and sex-standardized group values
were used to obtain Mahalanobis generalized distances (d2) between each pair of samples. The diagonal
matrix of Mahalanobis d2 values is provided in Table
4. The signicance of pairwise d2 distance contrasts for
those samples in which individual data were available
were assessed by means of F-tests, conducted according to the method of Konigsberg et al. (1993).
The diagonal matrix of Mahalanobis d2 values was
used as input for cluster analyses. Different associating algorithms were used to provide two perspectives on the patterning of intersample phenetic afnities. These associating algorithms include the
weighted pair average linkage method (WPGMA)
(Sneath and Sokol, 1973) and the neighbor-joining
method (Felsenstein, 1989; Saitou and Nei, 1987).
The cophenetic correlation coefcient, rcs (Sneath
and Sokol, 1973), was computed with the NTSYS-pc
statistical package to measure the degree of correspondence between the obtained phenogram from
WPGMA cluster analysis and the original resemblance matrix.
The diagonal matrix of Mahalanobis d2 values was
used as input for nonmetric multidimensional scaling, to provide a third perspective on the patterning
of intersample afnities. The coefcient of alienation
of Guttman (1968) was used to calculate distances
between individual points. The goodness of t obtained by multidimensional scaling was assessed
through calculation of the degree of stress through
100 iterations. Multidimensional scaling was accomplished with the SYSTAT statistical package
(Wilkinson, 1990). Results obtained were ordinated
in three-dimensional space, and a minimum spanning tree (Hartigan, 1975) was imposed on the array
Male sample
ADM
AFA
AFM
ALT
ALW
AND
CEMH
DJR
GKS
HAI
HAR
KAM
KAR
KOK
KRO
KUZ
MOL
QAW
SAMB
SAP
SHS
TH2
TH3
TMG
TMM
Female sample
ADM
AFA
AFM
ALT
ALW
AND
CEMH
DJR
GKS
HAI
HAR
KAM
KAR
KOK
KRO
KUZ
MOL
QAW
SAMB
SAP
SHS
TH2
TH3
TMG
TMM
Sex-standardized sample
ADM
AFA
AFM
ALT
AND
ALW
CEMH
DJR
GKS
HAI
HAR
KAM
KAR
KOK
KRO
KUZ
MOL
QAW
SAMB
SAP
SHS
TH2
TH3
TMG
TMM
1
GOL
BEB
NPH
NH
NB
OH
OB
BZB
186.0
191.7
192.1
189.5
184.2
186.4
188.2
186.9
190.1
176.4
187.3
183.0
194.8
186.1
187.9
190.9
185.6
183.0
189.3
183.5
185.8
188.8
188.4
190.2
188.4
145.0
142.4
144.1
135.9
141.9
140.4
141.3
134.7
134.5
138.4
134.5
147.4
134.9
138.1
139.1
138.9
138.1
137.9
137.1
134.9
136.4
132.0
134.1
132.0
136.9
67.8
71.7
71.8
70.7
68.7
69.2
67.9
69.9
71.1
69.7
69.2
73.4
72.6
68.4
74.4
68.7
69.4
66.5
76.7
70.2
70.2
70.3
69.8
70.3
71.8
50.2
53.1
52.1
51.6
52.2
51.5
50.8
50.7
52.0
52.4
51.4
51.6
51.2
51.5
53.6
49.6
51.5
50.9
53.8
51.3
50.6
50.4
50.6
50.0
51.6
25.8
27.1
26.1
25.2
25.0
25.4
26.3
24.8
25.5
27.3
26.5
25.8
26.6
23.5
24.6
26.4
25.1
26.2
23.8
24.2
25.7
25.1
25.4
22.9
24.7
31.7
32.3
32.9
32.4
33.1
32.9
32.9
30.9
33.0
33.6
33.2
33.7
31.8
30.9
34.1
30.9
31.8
31.6
35.0
32.7
31.8
31.6
32.1
33.3
31.2
44.4
43.7
44.9
40.7
39.0
42.1
41.3
37.5
40.1
38.7
41.4
44.1
42.5
43.2
38.6
39.9
38.3
40.5
42.0
37.7
42.1
41.0
41.2
41.5
42.4
140.7
141.6
138.4
129.1
130.8
131.8
134.8
131.3
127.6
134.0
131.5
139.7
129.9
133.4
131.0
134.0
126.6
136.2
128.3
129.1
129.4
125.3
127.3
133.0
131.8
175.9
182.6
180.4
181.4
173.9
177.6
179.2
184.7
185.8
170.6
180.9
173.2
183.0
177.6
181.0
179.3
183.5
178.1
180.1
181.5
179.1
178.3
179.4
180.2
179.8
140.6
138.2
135.8
135.1
135.3
136.0
132.4
134.0
132.9
135.0
132.1
143.4
132.1
136.4
133.5
132.6
134.2
128.8
136.5
134.1
133.3
132.1
131.8
130.9
133.2
67.5
64.8
67.4
67.3
64.9
67.3
62.7
69.5
69.8
65.4
66.2
68.0
67.5
66.2
69.0
65.1
70.6
62.6
69.5
67.5
67.6
67.6
66.1
66.6
69.2
48.9
47.8
49.5
49.6
49.4
48.4
46.0
50.2
50.9
49.3
48.3
48.4
47.9
49.4
50.6
46.8
49.7
47.4
48.4
49.2
50.0
48.3
48.3
48.1
49.2
23.9
25.4
25.6
24.2
24.2
24.6
24.4
25.6
25.2
26.0
24.2
24.6
24.7
23.8
24.1
23.6
25.0
24.5
23.4
24.8
24.5
23.7
23.9
22.9
23.7
33.0
31.1
33.1
32.7
32.0
32.2
33.3
33.0
32.9
32.8
34.1
32.9
32.0
31.8
33.2
30.7
32.6
32.3
32.1
33.0
31.9
33.6
31.7
33.1
31.9
42.5
46.5
44.3
38.9
37.5
41.8
39.9
38.5
39.0
37.6
40.6
42.1
41.6
41.2
36.8
36.3
38.8
38.9
39.3
37.2
40.7
38.7
39.6
40.0
40.9
127.4
129.8
131.8
121.4
124.4
128.2
119.5
123.9
123.4
125.6
123.9
131.8
123.8
128.5
129.5
122.4
126.5
125.0
122.5
124.4
122.7
118.7
120.2
122.3
124.5
181.0
187.3
186.3
185.5
182.0
179.0
183.7
185.8
190.1
173.5
184.1
178.1
188.9
181.9
184.4
185.1
184.5
180.5
184.7
182.5
182.5
183.5
183.9
185.2
184.1
142.8
140.3
140.0
135.5
138.2
138.6
136.8
134.3
134.5
136.7
133.3
145.4
133.5
137.3
136.3
135.7
136.1
133.3
136.8
134.5
134.8
132.1
133.0
131.5
135.1
67.7
68.3
69.6
69.0
68.3
66.8
65.3
69.7
71.1
67.5
67.7
70.7
70.1
67.3
71.7
66.9
70.0
64.5
73.1
68.8
68.9
69.0
69.9
68.4
70.5
49.6
50.5
50.8
50.6
50.0
50.8
48.4
50.5
52.0
50.8
49.9
50.0
49.6
50.5
52.1
48.2
50.6
49.1
51.1
50.2
50.3
49.4
49.4
49.1
50.4
24.9
26.3
25.9
24.7
25.0
24.6
25.3
25.2
25.5
26.7
25.4
25.2
25.7
23.7
24.4
25.0
25.1
25.3
23.6
24.5
25.1
24.4
24.7
22.9
24.2
32.4
31.7
33.0
32.6
32.2
32.6
33.1
32.0
33.0
33.2
33.6
33.3
31.9
31.4
33.7
30.8
32.2
32.0
33.6
32.9
31.8
32.6
31.9
33.2
31.6
43.5
45.1
44.6
39.8
42.6
38.3
40.6
38.0
40.1
38.1
41.0
43.1
42.1
42.2
37.7
38.1
38.6
39.7
40.7
37.5
41.4
39.9
40.4
40.8
41.7
134.1
135.7
135.1
125.3
132.4
127.6
127.1
127.6
127.6
129.8
127.7
135.8
126.9
131.0
130.2
128.2
126.5
130.6
125.4
126.7
126.0
122.0
123.8
127.7
128.2
Abbreviations for craniometric variables are from Table 2. Abbreviations for samples are from Table 1.
208
0.0
12.042
4.187
6.375
5.530
4.176
3.979
2.069
6.149
3.544
3.893
3.077
2.941
2.211
4.880
0.0
12.367
6.724
13.567
12.471
11.105
10.941
9.208
13.146
8.204
12.896
14.296
12.344
8.076
0.0
6.035
9.922
5.182
4.189
7.091
3.535
7.571
1.521
1.573
1.152
4.028
1.675
0.0
9.700 0.0
6.472 3.445
6.280 1.954
4.269 5.783
2.158 9.440
8.194 0.597
2.439 7.851
5.886 6.162
2.811 10.382
4.318 5.786
6.790 7.567
0.0
1.342
3.558
5.838
1.812
4.700
4.035
3.426
4.666
4.565
0.0
4.544
2.676
0.962
2.952
2.019
2.122
4.459
3.367
0.0
9.440
3.814
4.579
6.049
4.669
4.688
5.782
0.0
4.895
2.854
1.873
5.995
3.790
2.403
0.0
5.733
4.016
4.387
4.593
6.126
0.0
1.427
0.586
3.940
0.754
0.0
0.384
2.828
2.121
0.0
5.276
0.689
0.0
2.863
0.0
0.0
9.582
3.435
14.601
2.576
6.834
3.804
3.154
1.296
5.180
3.313
2.731
2.866
1.617
1.656
3.696
3.535
RESULTS
0.0
2.879
3.870
2.006
1.671
0.969
7.800
3.114
10.608
2.526
4.381
3.878
2.519
0.759
4.270
2.009
2.298
1.296
0.726
0.608
3.044
2.106
0.0
0.651
8.216
11.187
1.900
5.942
12.879
9.969
14.863
8.921
6.396
5.592
3.160
16.850
10.922
10.987
7.599
10.378
14.700
4.366
9.497
6.399
9.195
4.800
0.0
6.208
8.787
0.953
4.134
10.467
7.823
11.760
6.318
4.352
4.677
2.804
12.914
9.408
8.567
6.263
7.277
11.396
3.326
7.309
7.828
6.706
3.713
0.0
4.961
3.396
3.169
4.836
3.043
5.479
9.040
9.317
5.416
2.903
3.537
2.327
3.055
6.324
1.963
4.932
5.768
6.390
6.898
6.273
0.0
2.864
6.790
6.037
7.931
4.355
3.695
4.242
1.076
8.714
5.703
5.304
3.435
5.297
7.188
1.865
5.137
4.106
4.411
2.000
0.0
4.367
3.465
6.800
2.029
8.526
4.002
4.722
6.607
3.748
3.399
2.581
5.477
4.240
2.815
3.163
2.410
4.033
4.564
0.0
1.429
6.824
3.727
14.107
5.058
7.647
1.593
0.952
0.428
4.154
4.431
0.669
4.432
2.963
3.045
4.462
4.608
0.0
6.989
9.924
14.058
10.962
11.857
7.896
6.218
4.693
5.297
4.981
8.819
10.480
12.592
12.528
11.403
KUZ
KRO
KOK
KAR
KAM
HAR
HAI
GKS
DJP
AND CEMH
ALW
ALT
AFM
AFA
ADM
0.0
2.146
1.423
7.482
7.237
1.094
5.033
11.681
10.844
10.554
8.735
1.752
8.138
2.481
13.039
9.531
9.209
6.914
8.160
11.583
4.751
9.455
8.245
8.486
4.901
ADM
AFA
AFM
ALT
ALW
AND
CEMH
DJR
GKS
HAI
HAR
KAM
KAR
KOK
KRO
KUZ
MOL
QAW
SAMB
SAP
SHS
TH2
TH3
TMG
TMM
MOL
QAW SAMB
SAP
SHS
TH2
TH3
TMG TMM
The bias-adjusted matrix of Mahalanobis d2 values was calculated according to the procedures outlined above (Table 4). F-tests for those 16 samples in
which individual data are available (Table 5) reveal
that the majority of d2 values between samples are
signicant (98/120; 81.7%). Of the 98 pairwise contrasts exhibiting a signicant difference, 7 (7.1%)
are signicant at the 0.05 level, while 91 (92.9%) are
signicant at the 0.01 level.
WPGMA cluster analysis
The dendrogram obtained by means of the
WPGMA associating algorithm (Fig. 2) indicates
that the Hainan sample (HAI) from south China
represents the most divergent of all samples considered. The major division among remaining samples
occurs between steppe samples (except SAMB and
TMM) and all other samples. Bactrian samples are
segregated from samples obtained from Iran, Turk-
209
INHABITANTS OF XINJIANG
TABLE 5. F-tests and probability values of pairwise mahalanobis d2 generalized distances1
ALT
ALW
CEMH
DJR
GKS
HAI
HAR
KRO
KUZ
MOL
QAW
SAP
SHS
TH2
TH3
TMG
ALT
ALW
CEMH
DJR
GKS
HAI
HAR
KRO
KUZ
MOL
QAW
SAP
SHS
TH2
TH3
TMG
0.000
9.423
3.254
4.512
3.443
31.612
9.300
1.975
4.251
1.839
6.043
4.585
4.919
1.027
2.948
4.308
0.003
0.000
5.378
8.280
16.507
11.799
15.797
1.457
5.825
5.467
4.228
3.812
17.950
7.983
29.446
9.547
0.000
0.000
0.000
0.001
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.007
0.000
0.000
0.000
0.067
0.197
0.086
0.660
0.066
0.000
0.018
0.000
0.000
0.004
0.228
0.000
0.000
0.000
0.359
0.081
0.000
0.001
0.554
0.003
0.000
0.000
0.564
0.102
0.000
0.000
0.061
0.000
0.000
0.000
0.014
0.187
0.012
0.000
0.000
0.001
0.001
0.358
0.000
0.000
0.000
0.980
0.061
0.183
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.425
0.000
0.026
0.002
0.027
0.000
0.014
0.162
0.006
0.038
0.002
0.002
0.041
0.004
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.000
0.001
0.733
0.000
0.000
0.008
0.000
0.000
0.000
0.009
0.187
0.003
0.000
0.008
0.001
0.000
0.070
0.000
6.102
5.769
12.222
3.031
2.229
3.701
4.406
2.208
4.768
4.874
2.706
4.768
3.450
4.002
21.312
9.003
0.735
1.380
0.861
5.113
1.130
13.115
3.647
10.984
5.492
40.812
10.669
1.969
5.468
3.247
7.511
5.613
11.404
2.345
8.508
5.359
24.431
6.421
14.805
17.226
7.301
11.172
40.557
16.304
77.572
19.491
2.672
6.481
8.291
2.712
6.447
12.834
4.033
12.042
2.898
1.198
0.854
1.739
0.233
4.160
1.853
5.928
1.740
1.802
3.139
2.107
8.480
3.560
7.091
4.117
5.209
1.497
7.782
2.314
6.702
5.111
3.816
6.883
4.638
7.929
3.594
12.318
4.019
11.006
4.596
2.145
3.294
5.922
0.652
2.168
8.960
F-values are below diagonal. Probability values (P-values) are above diagonal. Abbreviations for samples are from Table 1. Only those
samples with individual data are included. This resulted in elimination of Andronovo-Minusinsk (ADM), Afanasievo-Altai (AFA),
Afanasievo-Minusinsk (AFM), Andronovo-Kazakhstan (AND), Karasuk-Minusinsk (KAM), Kara depe (KAR), Kokcha III (KOK),
Samtavro (SAMB), and Tigrovija Balka-Makoni Mor (TMM).
menistan, and the Indus Valley. The two later samples from Xinjiang (ALW and KRO) are associated
with the Bactrian samples. Kroran (KRO) features a
very close afnity with the earliest of the Bactrian
samples (SAP), while Alwighul (ALW) joins the later
Bactrian samples (DJR, KUZ, and MOL) at a more
distant remove. Indus Valley samples are identied
as sharing slightly closer afnity to samples from
Iran and Turkmenistan than to Bactrian samples.
Afnities among Indus Valley samples are rather
diffuse. In fact, the early sample from western
China, Qawrighul (QAW), is identied as possessing
closer afnities to the two samples from Harappa
(HAR and CEMH) than exhibited by the third Indus
Valley sample, Timargarha (TMG). The remaining
210
Fig. 3.
Multidimensional scaling
Multidimensional scaling of the bias-adjusted diagonal matrix of d2 values into three dimensions
with the coefcient of alienation of Guttman (1968)
is accomplished with a stress value of 0.097 after
100 iterations. This value falls within acceptable
limits, and indicates that multidimensional scaling
of these data into three dimensions provides an array of intersample associations only mildly affected
by distortion. A plot of multidimensionally scaled
values, with a minimum spanning tree imposed
between individual data points, is provided in Figure 4.
An examination of this array conrms the patterns of interregional afnities identied by neighbor-joining cluster analysis (Fig. 3). Hainan (HAI)
reects the most divergent sample. The two later
western Chinese samples, Kroran (KRO) and Alwighul (ALW), feature the closest afnities to Sapalli
(SAP), the earliest of the Bactrian samples. Two of
the samples from Turkmenistan (Altyn depe (ALT)
and Geoksyur (GKS)) span the phenetic space between Iranian samples and Bactrian samples, with
Geoksyur exhibiting closer phenetic afnities to
Bactrians (especially the latest sample, Molali
(MOL)), while Altyn depe shares closer phenetic afnities to Iranians. The steppe Bronze Age sample
from the Caucasus (SAMB) represents a phenetic
outlier to all other samples, exhibiting only a very
distant afnity to the sample from Altyn depe. Indus
Valley samples share rather close afnities to one
another but are strongly segregated from all other
samples, except the early western Chinese sample
from Qawrighul (QAW).
All steppe Bronze Age samples, except Samtavro
(SAMB), are found on the left side of the array.
Intersample afnities among the Karasuk (KAM),
Afanasievo (AFA and AFM), and Andronovo (AND
and ADM) samples are relatively close. However,
INHABITANTS OF XINJIANG
211
Fig. 4. Minimally spanned plot of sample values for rst three multidimensionally scaled dimensions. Sample abbreviations from
Table 1. Xinjiang samples (QAW, ALW, and KRO) and Chinese sample from Hainan (HAI) are represented by asterisks; North
Bactrian samples, by stars; Iranian samples, by pentagons; Turkmenian, Caucasus, and Tajik samples, by triangles; Indus Valley
samples, by circles; and Russo-Kazakh samples, by squares.
212
Fig. 5. Minimally spanned ordination of sample scores for rst three principal coordinate axes. Sample abbreviations from Table
1. Xinjiang samples (QAW, ALW, and KRO) and Chinese sample from Hainan (HAI) are represented by asterisks; North Bactrian
samples, by stars; Iranian samples, by pentagons; Turkmenian, Caucasus, and Tajik samples, by triangles; Indus Valley samples, by
circles; and Russo-Kazakh samples, by squares.
INHABITANTS OF XINJIANG
213
214
trans-Ural region in the west to the Minusinsk Basin in the east. In this case, the close similarities in
archaeological assemblages attributed to Andronovo
and Afanasievo archaeological horizons do appear to
document an eastward and southward population
expansion.
Nevertheless, there is no support for the hypothesis that steppe populations contributed signicantly to Bronze Age populations of the Tarim Basin. Despite numerous similarities between
Afanasievo and Andronovo artifacts and Bronze Age
artifacts from Xinjiang (Bunker, 1998; Chen and
Hiebert, 1995; Kuzmina, 1998; Mei and Shell, 1998;
Peng, 1998), all analyses of phenetic relationships
consistently reveal a profound phenetic separation
between steppe samples and the samples from the
Tarim Basin (Qawrighul, Alwighul, and Kroran).
Further, neither of the later Tarim Basin samples
from Alwighul or Kroran appears phenetically closer
to the Han Chinese sample from Hainan, thereby
indicating an absence of East Asian inuence in
these samples.
The second model offered to account for the origins
of the Bronze Age inhabitants of the Tarim Basin is
the Bactrian oasis hypothesis (Askarov, 1973, 1981,
1988; Barber, 1999). Proponents of this model emphasize the similarity in environmental conditions
between the oases skirting the Taklamakan Desert
and those found in Bactria and Margiana to the
west. Proponents of the Bactrian oasis model argue
that the very skills developed by the founders and
occupants of the urban centers of the Oxus civilization (irrigation agriculture, development of extensive trade networks between locally resource-impoverished oases, and domestication of sheep and goats)
are exactly those that accompany the initial appearance of Bronze Age populations in the Tarim Basin
(Barber, 1999; Chen and Hiebert, 1995). To explain
the changes in textile manufacture, clothing styles,
and metallurgical technology found in the Tarim
Basin beginning around 1200 B.C., some proponents
of the oasis model concur with the steppe hypothesis
and envisage a second inux of colonists from the
steppelands (Barber, 1999)
If this model is true, the earliest Tarim Basin
populations, such as Qawrighul, should possess
close similarities to samples from Bactria. Given
that the nature of this interaction is thought to have
been unidirectional, from Bactria to the Tarim Basin, and limited in duration, phenetic afnities between populations of the two regions should initially
be close and then progressively decrease over time
as the two gene pools became increasingly distinct
due to genetic drift. Tarim Basin inhabitants that
postdate 1200 B.C. should represent the impact of
Andronovo immigrants from the Russo-Kazakh
steppe. Later Bronze Age inhabitants of the Tarim
Basin should be marked by a reduction in phenetic
distance to steppe populations in general, and to
Andronovo samples in particular. Phenetic afnities
possessed by the samples from Alwighul and Kroran
INHABITANTS OF XINJIANG
potheses admit the presence, albeit scarce, of a series of Neolithic sites in the basin that antedate the
initial Bronze Age (An, 1992a; Bergman, 1939;
Chang, 1977; Chen and Hiebert, 1995; Chen, 1990;
IAX, 1989; Mallory, 1995; Olsen et al., 1988; Teilhard de Chardin and Young, 1932; Wang, 1985; Xu,
1995). The recovery of microliths on the surface in
association with painted ceramics at Yierkabake
and with plain red wares at Xingeer led Wang
(1985) to suggest that the transition from the Neolithic to the Bronze Age, in at least the eastern
portion of the Tarim Basin, was one of cultural continuity rather than an unprecedented introduction
of a foreign Bronze Age cultural complex.
If a resident population, regardless of ultimate
derivation, was present in the Tarim Basin at the
emergence of the Bronze Age, initiation of the
Bronze Age in this region may have been the product
of a more subtle interaction between this local population and groups from adjacent regions. From a
biological perspective, such interactions may have
involved limited levels of unidirectional or bidirectional gene ow. Under such conditions, the biological impact of emigrants from outside would likely
be muted relative to the impact of outright wholesale colonization of an essentially unpopulated, or
minimally populated, region (Ayala, 1982; Bodmer
and Cavalli-Sforza, 1975; Cavalli-Sforza et al., 1994;
Cummings, 1997; Fix, 1999; Weiss, 1988; Wijsman
and Cavalli-Sforza, 1984). Unless by some fortuitous
circumstance the remains recovered from Qawrighul are those of some foreign entrepot, these remains should reect the impact of such gene ow by
moderate to low afnities to those adjacent, nonTarim Basin populations with whom they were in
contact.
The results, however, fail to demonstrate even a
low-level phenetic afnity between Qawrighul and
either steppe samples or samples from Oxus civilization urban centers. Not only is there no evidence
for substantial immigration into the Tarim Basin by
populations of these two adjacent regions; it also
appears unlikely that either steppe populations or
Oxus civilization populations served as a source of
any signicant gene ow commensurate with the
appearance of the Bronze Age occupation of Qawrighul. Given the paucity of contemporaneous skeletal
remains from other parts of the Tarim Basin, the
presence of immigrants from either the steppelands
or the urban centers of the Oxus civilization cannot
be denitively ruled out.
The second alternative explanation to account for
the human remains from Qawrighul is that they are
the product of emigration from a source area other
than the Russo-Kazakh steppelands or Oxus civilization urban centers. While the results obtained
indicate that there is no evidence that gene ow
from either steppe or Oxus civilization populations
led to the establishment of the Qawrighul population, all analyses, except neighbor-joining cluster
analysis (Fig. 3), disclose a low-level afnity be-
215
216
217
INHABITANTS OF XINJIANG
218
INHABITANTS OF XINJIANG
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