Raw material variability as archaeological tools: Preliminary results from a geochemical study of the basalt vessel workshop at Iron Age Tel Hazor, Israel

Tatjana Gluhak 1, Danny Rosenberg 2, Jennie Ebeling 3

1. Institute of Geosciences, Johannes Gutenberg University, Mainz, Germany.  Email: gluhak@uni-mainz.de
2. Laboratory for Ground Stone Tools Research, Zinman Institute of Archaeology, University of Haifa, Haifa, Israel.  Email: drosenberg@research.haifa.ac.il
3. Department of Archaeology and Art History, University of Evansville, Evansville, IN, U.S.A.  Email: je55@evansville.edu

 

 

 

Abstract:

The discovery of a basalt vessel workshop at Tel Hazor, one of the most important Iron Age sites in the Near East, marks a turning point in our understanding of stone artefact production and distribution during the 1st millennium BCE. It offers a rare opportunity to characterize ancient raw material sources, production sites, and study production, trade and distribution systems. The basalt vessel workshop, the only one of its kind in the Levant, produced large quantities of bowl preforms and production waste. To better understand the production and distribution systems behind this specialized production centre, in 2011 we initiated a focused geochemical project that concentrated on the products of this unique workshop.  We measured the major and trace element composition of 44 unfinished basalt vessels from the workshop and other contexts at Hazor, and can demonstrate that the majority of these objects were derived from one specific, geochemically well-constrained, basaltic rock source. Only a few bowls clearly deviate from this geochemical composition and were produced using raw material from other sources. Thus, we believe that one major quarry existed that supplied the Hazor workshop with the majority of the basaltic raw material. The products from this specific extraction site provide us with a “Hazor reference group” that can be used to test whether or not finished vessels from Hazor and contemporary sites were produced in the Hazor workshop.

 

Keywords: ground stone tools; basalt vessels; workshop; geochemistry; Iron Age; Tel Hazor; Israel

 

 

1. Introduction

Finely-carved basalt vessels were both functional tools and status objects in the Iron Age (ca. 1200-586 BCE) southern Levant and their ubiquity in archaeological contexts throughout the region, including areas lacking basalt deposits, demonstrates their value to the Iron Age population. Although many goods, including textiles, spices, oils, and metals, were acquired over long distances during the Iron Age, few are amenable to provenance study. Stone artefacts, on the other hand, “have a far greater potential for elucidating long distance trade networks, as they are relatively common, virtually indestructible and do not generally undergo chemical or physical changes during their manufacture, use or subsequent deposition” (Rutter et al. 2003: 209). The recent discovery of a workshop for the manufacture of basalt vessels in a 9th century BCE context at Hazor (Ebeling & Rosenberg 2015) provides a unique opportunity to investigate aspects of the manufacture and distribution of this well-known but little-understood aspect of Israelite material culture.

Stone vessels found in Egypt and the eastern Mediterranean world have been the focus of archaeological interest during the past two decades. Stocks’ studies (1993; 1999; 2003) of the manufacture of hard stone objects, including vessels, sarcophagi, and statues, in ancient Egypt using archaeological, ethnographic, and experimental approaches, have shed much light on our understanding of manufacturing methods, especially the manufacture of vessels made of hard stone like basalt. Bevan (2007: 1), in his study of stone vessels and values in the Mediterranean Bronze Age, states that stone vessels are desirable sources of study for, among other reasons, their virtual indestructibility, the subtractive properties of stone, and the potential for macroscopic, petrographic, and geochemical provenance study. In her study of 2nd millennium BCE stone vessels in the Levant, Sparks (2007: 179-183) describes the evidence for the manufacture of obsidian and granite vessels at Middle Bronze Age Atchana (Alalakh) in southern Turkey and the manufacture of gypsum vessels at Middle Bronze II-Late Bronze Age Bet Shean in Israel.

A number of provenance studies have been conducted on basalt artefacts dated to different periods in the region since the 1980s, but these past attempts produced rather limited results and were only able to constrain larger regions (e.g., Amiran & Porat 1984; Philip & Williams-Thorpe 1993; 2000; 2001; Williams-Thorpe & Thorpe 1993; Rowan 1998; Rutter 2003; Rutter et al. 2003: 210; Watts et al. 2004; Rutter & Philip 2008). Petrographic studies either did not include detailed geochemical analyses (Amiran & Porat 1984) or focused solely on the artefacts without an intensive geochemical study of the potential basaltic raw material in the field. In their analyses, Philip & Williams-Thorpe, who only included 21 geological samples from Jordan (Philip & Williams-Thorpe 1993) and later added eight geological field samples (Philip & Williams-Thorpe 2001), stressed that more exact provenance determinations would only be possible with a more elaborate study of the basaltic rocks themselves and the establishment of a source database that facilitates statistical evaluations (Philip & Williams-Thorpe 2001).

The studies of Rutter (2003), Rutter & Philip (2008), and Rutter et al. (2003) concentrated on artefacts as well as the evaluation of trace element analyses; however, they left out basic analyses of rock types as well as an elaborate evaluation of their major element compositions. Furthermore, they based their constriction of the volcanic rocks in the region on a very small number of geological field samples in addition to those collected by Philip and Williams-Thorpe (1993; 2001). However, these authors, especially Rutter et al. (2003), stress that more geological samples must be analysed to gain a clearer picture of artefact provenance. An intensive study of the raw material variability of the artefacts connected to statistical evaluations was not conducted in any of the studies. Geochemical analyses undertaken in the 1980s led Xenophontos et al. (1988: 181) to speculate that Hazor may have been a centre for the trade in basalt vessels to Cyprus in the Late Bronze Age and Roman periods, although the authors of this study could not distinguish between the Syrian, Palestinian, and Jordanian basalt sources.

The geochemical analyses conducted by Rutter (2003) using ICP-MS (inductively coupled plasma mass spectrometry) suggest that ground stone artefacts found at Hazor were carved from basalt sources in the north Jordan Valley, Golan Heights, and Mt. Hermon regions (Rutter 2003: table 8:11). However, as stated above, these studies reflect the potential of provenance studies while also demonstrating the problems inherent in these studies, in particular the need for a reliable geochemical database of basalt sources. A large-scale project was recently initiated that focuses on establishing the geochemical signature of basalt sources in Israel using a basanite bifacial tool quarry and production site in the Manasseh Hills at the western fringes of the Jezreel Valley as a test case for the chosen methodology (Gluhak & Rosenberg 2013; Rosenberg & Gluhak 2016). The results of the study proved that a high-resolution sampling strategy, the geochemical analyses chosen, and statistical, multivariate analyses (see methodology section, below), provide a good combination for studying the provenance of basaltic tools. This was the springboard for the current study.

In 2010, the first workshop for the production of basalt vessels identified in the Levant was discovered at Hazor in northern Galilee. The largest Bronze and Iron Age tell site in northern Israel, Yadin excavated Hazor between 1955-1958 and again in 1968; the current excavation project directed by Ben-Tor commenced in 1990 (Ben-Tor 1989; Ben-Tor & Bonfil 1997; Ben-Tor & Zuckerman 2010). During 25 excavation seasons, thousands of ground stone tools, vessels, and other stone artefacts have been excavated from Bronze Age, Iron Age, and Persian Period contexts (Ebeling 2012). Located on the northern edge of Tel Hazor, the workshop was identified in a space defined by walls to the north and east with baulks up to three metres high to the west and south.

Two dozen blanks and unfinished basalt vessels of several types were associated with the workshop and the floors and fills contained flint tools, basalt hammerstones, and basalt production waste, as well as two iron chisels, a silver earring, spindle whorls, shells, and a zoomorphic figurine (Ebeling & Rosenberg 2015). In addition, 25 unfinished basalt vessels excavated between the 1990 and 2007 seasons in various contexts on the tell were also identified during analysis of the large ground-stone assemblage; at least two, although probably several others as well, were found in Late Bronze Age contexts, suggesting that an earlier basalt vessel industry also existed at the site. Forty-four samples from the total assemblage of 49 vessels were selected for geochemical analysis.

Geologically, Tel Hazor is located in the southwestern part of the Hula Valley in close vicinity to basaltic rocks that could have served as raw material for vessel production. The Hula Valley is a pull-apart basin along the Dead Sea transform filled with lacustrine and clastic sediments reaching a thickness of up to 3.5 km (e.g., Schattner & Weinberger 2008). Plio- to Pleistocene volcanic units are intercalated in the basin fill that can be stratigraphically connected to the Hasbani basalt in the north, the Golan volcanic rocks to the east, the Korazin block to the south, or the Dalton basalt in the southwest. In the immediate surroundings of Tel Hazor, where creeks cut the basin sediments, small outcrops of Pliocene Dalton basalt occur, whereas further to the east and southeast of Tel Hazor, the basaltic rocks cropping out within the basin sediments can be linked to the Ruman Yarda flows of the Golan volcanic massif that borders the Hula Basin in the east (see Figure 1) (Sneh & Weinberger 2006).

The purpose of the current geochemical-mineralogical analyses of the basalt vessels is to determine how many different basaltic raw materials sources were used by the craftspeople of Tel Hazor. The raw material variability within the present group of 44 basalt vessels offers important information about basaltic rock procurement as we can determine if the workshop was supplied with raw material from one or more specific basaltic rock extraction sites. This could suggest a close connection between extraction site and craftsperson, a more widespread procurement system, or even the absence of a well-defined procurement system for basaltic rock raw material. However, if within the group of basaltic vessels a specific rock can be identified geochemically as a dominant raw material used for vessel production at Tel Hazor, one or more “Tel Hazor reference groups” could be defined. These geochemical “reference groups” could serve in future basalt vessel provenance analyses as a basis to check whether or not a vessel found elsewhere was produced at Tel Hazor. Furthermore, assuming that one or more dominant extraction sites existed, the geochemical-mineralogical data of the artefacts serve as the basis to track their provenance when compared to geological samples collected in the field.

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 1 v2_resize.jpg

Figure 1: The geological situation of Tel Hazor in the southern Hula basin. Detail of the Rosh Pinah geological map (Sneh & Weinberger 2006).

 

2. Materials and methods

The vessels are produced from grey lava with up to 5% unevenly distributed vesicles in sub-mm to mm size. The only macroscopically visible phenocrysts are olivines, strongly altered to iddingsite. For the geochemical mineralogical analyses, a small piece was chipped off each of the 44 basaltic vessels. The sampling was conducted at the Laboratory for Groundstone Tools Research at the Zinman Institute of Archaeology at the University of Haifa. The samples were then sent to the Institute for Geosciences of the Johannes Gutenberg-University in Mainz. Seven samples were large enough to enable the production of thin sections for petrography. Weathered or carbonate crust was either removed by abrasion on a grinding wheel or by rinsing in HCl. Afterward, the samples were rinsed in distilled water in an ultrasonic bath, dried, and ground to powder manually in an agate mortar. As only a very limited amount of sample material was available and to avoid any contamination, the loss on ignition was determined in a platinum-cup on about 0.5-1.0 g of sample powder.

The same “ignited” material was used afterward for the geochemical analyses. To produce glass beads for major element determination by X-ray fluorescence, 0.4 g of ignited sample powder was fused with 5.2 g of Li2B4O7. The major element analyses were conducted in a 2002 model Philips MagXPRO wavelength-dispersive X-ray spectrometer with a Rh-X-ray tube and a maximum excitation of 3.2 kW. For trace element determination by Laser-Ablation-ICP-MS, approximately 40 mg of the sample powder was melted at 1200 °C to a glass bead in an iridium strip-heater. Three spots with a diameter of 100 μm each were measured on every glass bead using a pulse-rate of 10 Hz and laser energy densities of 6 J/cm² in an Agilent 7500 CE quadrupol ICP-MS, coupled to an ESI New Wave Research NWR193 (ArF-excimer) laser-ablation-system with 193 nm wavelength. The carrier gas was Argon. 43Ca served as the internal standard, its values taken from the XRF measurements. The reference materials NIST SRM 610 and NIST SRM 612 served as the external standards. The USGS-BCR-2G was measured for quality control. The values for NIST SRM 610, NIST SRM 612, and USGS-BCR-2G  were taken from the GeoRem Database (GeoRem preferred values, Jochum et al. 2005). Reproducibility and accuracy of the LA-ICP-MS analyses, monitored by repeated measurements of USGS-BCR-2G, are presented in Table 1. Data reduction and evaluation was conducted in MS excel. Results are presented in Table 2.

 

Table 1: Reproducibility and accuracy of the LA-ICP-MS analyses. Abbreviations: SD - standard deviation, RSD - relative standard deviation. GEOREM preferred values from Jochum et al. (2005).

 

USGS-BCR-2G

 

average (n=42)

SD

RSD %

GEOREM
preferred values

Sc

36.23

1.75

4.84

33

V

440.80

14.05

3.19

425

Cr

15.40

1.32

8.55

17

Mn

1611.47

73.94

4.59

1550

Co

38.10

1.61

4.23

38

Ni

12.32

0.89

7.20

13

Ga

21.74

0.96

4.42

23

Rb

47.49

2.57

5.41

47

Sr

330.43

9.32

2.82

342

Y

33.33

1.18

3.55

35

Zr

182.03

5.71

3.14

184

Nb

12.68

0.38

3.02

12.5

Ba

670.97

33.78

5.03

683

La

24.52

0.98

4.00

24.7

Ce

51.05

1.84

3.60

53.3

Pr

6.38

0.22

3.45

6.7

Nd

28.40

1.19

4.19

28.9

Sm

6.47

0.43

6.58

6.59

Eu

1.94

0.10

5.20

1.97

Gd

6.48

0.41

6.29

6.71

Tb

0.96

0.06

6.44

1.02

Dy

6.19

0.34

5.46

6.44

Ho

1.23

0.08

6.57

1.27

Er

3.64

0.21

5.82

3.70

Tm

0.48

0.04

8.08

0.51

Yb

3.28

0.22

6.79

3.39

Lu

0.48

0.04

8.94

0.50

Hf

4.87

0.26

5.37

4.84

Ta

0.73

0.04

6.01

0.78

Th

5.88

0.28

4.75

5.90

U

1.68

0.09

5.47

1.69

 

 

Table 2. Major and trace element composition of the Tel Hazor basalt vessels. Abbreviations: RMS - root mean square.

 

Haz1

Haz2

Haz3

Haz4

Haz5

Haz6

Haz7

Haz8

Haz9

Haz10

Haz11

Haz12

Haz13

Haz14

Haz15

SiO2 (%)

48.42

48.95

48.77

49.01

48.89

49.00

47.95

48.37

48.97

48.22

48.80

48.83

48.70

48.06

48.89

Al2O3

15.01

15.94

15.26

15.76

15.50

15.62

15.35

15.08

15.51

15.70

15.81

15.62

15.57

15.32

15.43

Fe2O3(t)

13.42

12.62

12.97

12.67

12.72

12.88

12.73

13.10

12.92

12.18

12.96

12.80

12.78

12.43

12.96

MgO

7.26

6.30

7.24

6.42

6.70

6.72

6.65

7.55

6.25

6.04

6.73

6.78

6.79

6.61

7.05

CaO

9.42

9.74

9.39

9.95

9.77

9.65

10.90

9.23

9.84

11.60

9.29

9.30

9.60

11.41

9.56

Na2O

3.07

3.14

3.02

3.15

3.13

3.14

3.04

3.02

2.96

3.11

3.10

3.13

3.12

3.10

3.12

K2O

0.94

0.83

0.88

0.89

0.91

0.88

0.85

0.81

0.88

0.83

0.87

0.90

0.87

0.89

0.84

TiO2

2.16

2.00

2.05

2.09

2.11

2.05

2.05

2.03

2.16

1.94

2.06

2.04

1.99

2.01

2.07

P2O5

0.50

0.40

0.44

0.44

0.44

0.45

0.44

0.38

0.42

0.42

0.45

0.45

0.38

0.45

0.40

sum

100.20

99.92

100.02

100.38

100.17

100.39

99.96

99.57

99.91

100.04

100.07

99.85

99.80

100.28

100.32

LOI

0.52

0.05

0.09

0.56

0.00

0.00

1.35

0.00

0.52

1.42

0.17

0.13

0.17

1.58

0.00

 

                             

Sc (ppm)

26

24

27

27

27

26

25

25

27

25

31

27

26

25

27

V

223

195

231

214

205

233

214

220

231

205

206

219

218

210

219

Cr

266

183

347

292

223

251

240

250

276

267

220

244

254

305

247

Mn

1327

1221

1448

1426

1264

1311

1331

1433

1243

1233

1288

1311

1265

1313

1334

Co

48

40

51

47

43

47

46

51

39

42

48

45

47

45

49

Ni

135

68

135

105

94

110

109

148

76

77

116

113

130

106

133

Ga

21

21

22

22

21

21

21

22

21

20

23

22

21

22

22

Rb

12

13

12

13

12

10

12

12

12

11

13

13

13

12

12

Sr

555

533

570

585

588

589

579

484

493

530

598

591

503

578

523

Y

23

20

21

38

20

20

19

20

22

19

23

23

19

27

22

Zr

170

145

164

155

148

152

148

139

157

143

176

156

142

148

163

Nb

30.9

31.3

24.7

27.5

25.9

26.1

25.9

24.2

34.9

30.6

33.3

26.8

24.9

27.2

29.4

Ba

299

262

295

319

281

282

296

247

237

294

300

318

261

284

259

La

26.5

20.8

24.8

24.4

24.3

24.2

23.0

20.3

22.4

20.3

26.7

27.4

19.8

24.2

23.7

Ce

51.7

40.8

50.8

49.6

48.0

48.5

46.2

42.4

43.0

42.7

50.3

54.3

39.9

49.1

45.9

Pr

6.4

5.2

6.1

5.9

5.8

5.7

5.6

5.1

5.7

5.1

6.2

6.5

4.8

5.8

5.6

Nd

27.0

22.0

25.7

25.0

25.1

24.1

24.0

21.7

24.7

22.3

27.2

28.1

21.4

24.6

24.7

Sm

5.85

5.05

5.22

5.60

5.70

5.41

4.92

5.03

5.39

5.02

6.11

5.90

4.84

5.37

5.50

Eu

1.92

1.70

1.95

2.00

1.85

1.82

1.79

1.69

1.85

1.84

1.95

2.01

1.66

1.88

2.03

Gd

5.39

4.71

5.34

5.01

4.74

5.26

4.77

4.39

5.30

4.52

5.85

5.89

4.41

4.50

5.66

Tb

0.79

0.69

0.73

0.69

0.73

0.71

0.71

0.67

0.75

0.66

0.77

0.81

0.68

0.70

0.80

Dy

4.69

3.86

4.14

4.17

4.08

4.12

4.00

3.97

4.52

3.95

4.77

4.87

3.94

4.04

4.86

Ho

0.81

0.73

0.83

0.76

0.80

0.70

0.70

0.75

0.85

0.72

0.89

0.85

0.72

0.73

0.87

Er

2.20

1.96

2.00

2.07

2.26

1.94

1.92

1.99

2.19

1.97

2.31

2.42

1.92

1.90

2.20

Tm

0.27

0.24

0.21

0.26

0.23

0.25

0.21

0.24

0.29

0.24

0.27

0.24

0.28

0.23

0.26

Yb

1.82

1.60

1.73

1.64

1.49

1.80

1.48

1.54

1.88

1.36

1.84

1.88

1.53

1.64

1.99

Lu

0.24

0.21

0.23

0.23

0.24

0.21

0.21

0.22

0.27

0.21

0.25

0.25

0.21

0.22

0.21

Hf

3.70

3.32

3.55

3.51

3.45

3.23

3.32

3.30

3.45

3.13

3.90

3.69

3.48

3.16

3.78

Ta

1.57

1.58

1.18

1.27

1.30

1.23

1.37

1.16

1.72

1.44

1.77

1.41

1.13

1.29

1.48

Th

2.33

1.78

2.09

2.20

2.06

2.08

2.10

1.77

2.05

1.84

2.54

2.39

1.70

2.17

2.18

U

0.55

0.51

0.46

0.50

0.50

0.46

0.52

0.47

0.51

0.50

0.63

0.51

0.47

0.58

0.55

 

 

 

Haz16

Haz17

Haz18

Haz19

Haz20

Haz21

Haz22

Haz23

Haz24

Haz25

Haz26

Haz27

Haz28

Haz29

Haz30

SiO2 (%)

49.09

44.69

48.55

49.11

47.73

48.86

48.86

48.70

48.35

48.61

47.29

49.12

49.10

45.43

43.42

Al2O3

15.90

13.13

15.73

15.62

15.67

15.92

15.62

16.28

16.14

16.42

14.51

15.66

15.83

14.86

13.89

Fe2O3(t)

12.45

13.42

12.28

12.91

12.40

13.30

12.94

12.30

13.50

13.69

13.02

12.79

12.80

13.11

13.01

MgO

6.16

9.91

6.07

6.60

6.37

5.46

6.85

5.77

5.74

5.25

9.09

6.36

6.42

8.49

7.13

CaO

9.99

10.65

10.98

9.34

10.94

9.78

9.40

9.77

9.52

9.55

10.37

9.36

9.50

10.38

14.15

Na2O

3.17

3.01

3.26

3.11

3.16

3.30

3.14

3.11

3.24

3.26

2.91

3.08

3.21

2.96

2.26

K2O

0.85

1.22

0.92

0.91

0.98

0.87

0.88

0.87

0.83

0.89

0.73

0.92

0.92

1.03

0.83

TiO2

2.11

2.56

2.07

2.07

2.11

2.15

2.05

2.03

2.13

2.19

1.78

2.08

2.13

2.84

2.99

P2O5

0.46

1.03

0.47

0.42

0.64

0.43

0.46

0.45

0.40

0.40

0.46

0.45

0.43

0.59

1.65

sum

100.18

99.62

100.33

100.09

100.00

100.07

100.20

99.28

99.85

100.26

100.16

99.82

100.34

99.69

99.33

LOI

0.00

0.44

0.95

0.22

0.68

0.94

0.23

0.36

0.94

0.79

0.74

0.62

0.26

1.66

7.15

 

                             

Sc (ppm)

27

23

25

24

27

27

25

24

28

32

25

26

25

29

24

V

217

203

204

210

228

240

219

209

229

241

176

216

222

210

232

Cr

239

326

235

232

281

302

250

181

283

288

285

240

308

194

242

Mn

1299

1477

1280

1229

1341

1322

1326

1305

1271

1273

1301

1248

1365

1415

1061

Co

41

56

43

45

46

46

47

41

51

51

54

43

46

49

39

Ni

73

224

90

122

102

110

119

62

142

125

225

94

115

175

137

Ga

22

21

21

22

22

23

21

22

23

24

19

19

23

20

20

Rb

13

20

12

14

16

12

12

13

13

12

12

13

14

7

17

Sr

520

959

587

538

653

514

564

525

500

526

507

822

548

738

2104

Y

22

23

21

20

23

23

20

22

23

24

19

21

20

24

27

Zr

172

226

157

145

183

158

162

163

158

166

136

157

149

208

239

Nb

39.1

63.6

28.0

24.2

39.5

27.1

28.2

36.0

24.9

28.7

23.3

26.9

27.0

51.4

110.8

Ba

256

501

287

323

344

258

308

263

267

273

237

1801

287

284

792

La

23.0

41.1

25.0

22.3

31.9

22.6

22.9

22.1

24.0

24.6

22.0

24.9

22.7

30.4

86.0

Ce

45.9

87.9

49.2

43.3

64.2

45.1

45.0

45.9

46.7

42.4

44.0

49.3

45.7

59.2

157.1

Pr

5.8

10.5

6.0

5.3

7.7

5.5

5.5

5.6

6.0

5.8

5.3

6.1

5.5

7.1

17.2

Nd

24.8

44.2

25.8

23.4

33.1

24.3

24.9

23.5

26.3

25.6

22.3

25.5

23.2

30.7

68.1

Sm

5.33

8.92

5.87

5.30

6.43

5.29

5.26

5.01

5.33

5.93

5.30

5.14

4.89

6.10

12.45

Eu

1.94

3.00

1.95

1.95

2.22

1.91

1.79

1.83

1.86

2.05

1.69

1.76

1.76

2.16

3.80

Gd

6.23

7.49

5.08

4.96

6.03

5.36

4.60

4.95

5.78

6.04

5.12

5.29

4.74

6.29

9.84

Tb

0.84

0.92

0.68

0.63

0.85

0.76

0.69

0.75

0.72

0.84

0.68

0.73

0.68

0.85

1.16

Dy

4.59

5.07

4.19

4.14

4.91

4.64

3.91

4.27

4.86

4.55

4.25

4.37

4.16

4.79

6.31

Ho

0.88

0.84

0.79

0.68

0.88

0.85

0.73

0.77

1.00

0.94

0.75

0.75

0.75

0.93

1.00

Er

2.11

2.15

2.06

2.01

1.99

2.33

1.99

2.09

2.25

2.49

1.76

2.00

1.97

2.46

2.37

Tm

0.28

0.26

0.23

0.29

0.29

0.27

0.27

0.25

0.32

0.34

0.22

0.26

0.23

0.30

0.30

Yb

1.71

1.61

1.70

1.51

1.72

1.86

1.73

1.76

1.83

1.86

1.60

1.64

1.70

1.76

1.79

Lu

0.21

0.19

0.21

0.22

0.22

0.22

0.22

0.26

0.22

0.23

0.16

0.21

0.21

0.26

0.24

Hf

3.87

4.76

3.67

3.22

3.77

3.57

3.89

3.64

3.53

4.01

2.86

3.55

3.41

4.66

5.11

Ta

2.04

3.08

1.38

1.27

2.22

1.41

1.62

1.75

1.27

1.41

1.42

1.30

1.30

2.83

4.96

Th

1.93

3.09

2.17

1.94

2.91

2.05

2.35

1.95

2.01

2.14

1.98

2.23

1.94

3.39

7.57

U

0.51

0.83

0.45

0.40

0.89

0.52

0.58

0.69

0.53

0.58

0.53

0.52

0.53

1.05

1.91

 

 

 

Haz31

Haz32

Haz33

Haz34

Haz35

Haz36

Haz37

Haz38

Haz39

Haz40

Haz41

Haz42

Haz43

Haz44

RMS

SiO2 (%)

46.91

47.63

48.24

48.80

48.77

49.11

48.14

48.67

48.73

49.10

49.09

47.80

49.23

49.02

0.4

Al2O3

14.22

14.91

15.96

15.74

15.57

16.35

15.52

15.66

16.10

16.58

16.12

14.89

16.67

15.79

0.5

Fe2O3(t)

12.54

12.61

12.35

12.42

13.25

12.92

14.45

12.85

13.16

12.92

12.74

13.04

12.17

12.94

0.6

MgO

9.36

7.86

5.03

6.53

6.80

5.88

6.77

6.62

5.82

4.93

6.37

8.31

5.47

6.60

0.4

CaO

9.75

10.18

12.21

9.82

9.43

9.30

9.15

9.97

9.30

9.53

9.74

9.94

10.07

9.34

0.4

Na2O

2.42

2.96

3.07

3.25

3.05

3.25

3.03

3.11

3.17

3.41

3.22

2.71

3.23

3.14

1.0

K2O

1.25

0.95

0.86

0.91

0.80

0.89

0.85

0.86

0.91

1.04

0.81

0.83

0.92

0.92

0.5

TiO2

2.53

2.13

2.29

2.13

2.08

2.10

2.01

2.06

2.10

2.24

2.05

1.90

2.04

2.13

0.5

P2O5

0.65

0.36

0.48

0.48

0.33

0.35

0.42

0.41

0.34

0.54

0.29

0.44

0.45

0.40

1.1

sum

99.63

99.59

100.49

100.08

100.08

100.15

100.34

100.21

99.63

100.29

100.43

99.86

100.25

100.28

 

LOI

2.22

0.56

2.42

-0.17

0.62

0.87

0.75

0.72

1.14

0.89

-0.01

0.65

0.32

0.66

 

 

                             

Sc (ppm)

24

27

27

25

26

27

26

22

23

27

25

27

24

26

 

V

202

251

380

214

256

252

265

245

219

287

308

231

256

237

 

Cr

247

408

145

246

313

230

353

219

200

255

205

336

170

269

 

Mn

1246

1545

1543

1324

1503

1603

1589

1630

1669

1490

1481

1476

1271

1498

 

Co

49

60

46

43

52

53

66

53

57

49

48

55

40

51

 

Ni

190

236

55

96

149

128

203

141

136

107

85

223

60

125

 

Ga

20

23

28

27

24

26

26

28

26

27

26

22

26

24

 

Rb

14

18

14

21

11

15

17

19

17

15

13

12

17

13

 

Sr

623

504

588

729

517

610

558

584

575

589

481

534

591

599

 

Y

22

33

24

20

29

19

21

19

18

28

20

29

23

28

 

Zr

177

149

197

147

138

161

160

153

132

185

122

135

182

160

 

Nb

37.3

34.1

46.6

25.3

23.9

27.5

31.0

26.5

22.3

34.5

24.5

26.4

35.7

28.1

 

Ba

218

406

277

421

308

340

343

343

424

352

264

247

301

340

 

La

27.7

16.6

23.8

24.3

17.6

20.2

21.9

21.1

20.0

29.7

16.4

21.9

22.1

21.4

 

Ce

56.1

40.4

58.3

54.5

38.8

44.7

46.7

51.0

50.4

59.1

35.6

49.3

46.2

48.6

 

Pr

6.8

4.5

6.8

5.9

4.6

5.0

5.5

5.5

5.2

7.2

4.1

5.6

5.7

5.5

 

Nd

29.3

19.9

30.6

25.6

20.6

22.0

23.2

23.4

22.6

31.3

19.5

24.6

24.6

24.4

 

Sm

6.55

4.68

6.33

5.79

4.83

4.51

4.93

4.75

4.87

6.58

4.35

5.40

5.67

5.11

 

Eu

2.31

1.62

2.24

1.95

1.68

1.84

1.83

1.83

1.85

2.17

1.70

1.75

1.89

1.80

 

Gd

5.95

4.40

6.52

5.46

4.47

4.53

5.03

4.84

4.42

6.90

4.43

4.90

5.44

4.94

 

Tb

0.83

0.54

0.93

0.74

0.63

0.62

0.69

0.58

0.60

0.89

0.53

0.74

0.75

0.65

 

Dy

4.39

3.58

5.24

4.87

3.86

3.66

4.44

3.87

3.95

5.48

3.18

4.14

4.49

3.96

 

Ho

0.77

0.57

0.87

0.66

0.74

0.69

0.78

0.70

0.60

1.02

0.57

0.70

0.85

0.71

 

Er

1.99

1.69

2.43

2.08

2.18

1.78

2.17

2.07

1.96

2.72

1.44

2.03

2.32

1.91

 

Tm

0.22

0.22

0.29

0.23

0.24

0.24

0.25

0.25

0.20

0.32

0.19

0.22

0.30

0.25

 

Yb

1.50

1.36

1.98

1.54

1.63

1.66

1.72

1.28

1.42

2.01

1.44

1.68

1.91

1.66

 

Lu

0.19

0.16

0.24

0.21

0.21

0.18

0.23

0.22

0.22

0.26

0.20

0.24

0.24

0.25

 

Hf

3.97

3.46

4.77

3.21

3.29

3.66

3.67

3.37

2.97

4.50

2.94

3.22

4.05

3.75

 

Ta

1.89

1.68

2.16

1.17

1.14

1.60

1.51

1.19

1.04

1.67

1.09

1.30

1.62

1.36

 

Th

2.57

1.68

2.37

2.28

1.68

2.00

1.94

2.00

1.81

2.53

2.21

2.06

1.98

2.04

 

U

0.73

0.45

0.63

0.70

0.54

0.64

0.62

0.70

0.51

0.75

0.50

0.43

0.70

0.59

 

 

3. Results

3.1. Major and trace element composition

The main goal of the present study is to use the geochemical data to determine whether or not multiple vessels were produced from a single basaltic rock source that represents a particular extraction site. However, products from a single extraction site will never show an identical geochemical composition because they always mirror the natural heterogeneity within a rock outcrop (Gluhak & Hofmeister 2009; 2011; Gluhak & Rosenberg 2013). Thus, two or more rocks can only be defined as the same on the basis of the similarity of their geochemical compositions, with “similarity” meaning a low variation in geochemical features.

According to the IUGS-recommendations for classification of fine-grained volcanic rocks (Le Maitre et al. 1989), the silica and alkali content of the samples are plotted in the TAS-diagram (Le Bas et al. 1986) (see Figure 2).

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 2 v2 -ed.jpg

Figure 2. Classification of the samples in the TAS-diagram.

 

The bulk of the samples are slightly alkaline basalts sensu stricto. Two samples are basanites according to their normative (i.e. CIPW-norm calculated) olivine content of greater than 10 %. Thirty-three of the vessels contain normative hypersthene up to 8.25 %, and the other eleven contain normative nepheline, up to 6.79 % (Table 3). The fact that the majority of vessels plot as a cluster in the basalt field of the TAS-diagram already hints at the use of a specific, preferred basalt occurrence. However, the difficulty in determining whether or not the majority of vessels were produced from the same outcrop, meaning from one (or more than one) extraction site, is shown in Figures 3a and 3b (Mg# versus Al2O3 and Mg# versus CaO). These figures show that the “basalt group,” which seems well-constrained in the TAS-diagram, shows large variations in other major elements. The Mg#-Al2O3-plot in Figure 3a e.g., displays the natural trend of a typical magmatic differentiation, from high Mg# - low alumina-content to low Mg# - high alumina-content, a trend that can display a general trend in basaltic rocks from a certain region but can also be present within a single basalt occurrence. Therefore, it cannot be determined based on the major element composition of the vessels alone if these variations are due to the natural inhomogeneity within one extraction site or if they indicate that the basalt vessels originate from more than one extraction site.

 

Table 3. CIPW-normative mineral content.

 

Av.

Min.

Max.

No.

Or

5.31

4.31

7.39

 

Ab

24.76

10.87

28.86

 

An

25.92

18.71

28.27

 

Di

17.02

13.65

28.12

 

Hy

3.19

1.12

8.25

33

Ol

16.26

11.74

22.56

 

mt

1.87

1.77

2.10

 

Il

4.05

3.38

5.68

 

Ap

1.05

0.63

3.60

 

ne

0.71

1.32

6.79

11

 

Trends of certain trace elements show us that the lavas were probably subjected to varying degrees of fractional crystallisation (Figure 4) during their development. The trace element patterns of the samples are presented in Figure 5. As intraplate volcanic rocks, characteristic for this region, the samples display the typical pattern of ocean island basalts (OIB). Again, the majority of samples display a very similar geochemical pattern. Two samples show higher trace element concentrations, a typical phenomenon for basanite rocks of the region. Thus, the trace elements offer even fewer characteristics to constrain rocks from each other than the major elements.

 

3.2. Multivariate evaluation

To determine if a Tel Hazor “core group” representative of a certain extraction site is present in our set of samples, we needed to decide which geochemical features within our group of measured elements are characteristic, i.e. which geochemical features can be used to constrain potential groups from each other. To do this, a principal component analysis (PCA) was conducted; although in the present study we do not have the ideal number of cases available for PCA (the number of cases should exceed at least three times the number of variables). All measured elements were entered as variables. Prior to PCA the data were log-transformed to ensure the independency of the compositional data and z-standardized, resulting in a mean of 0 and a standard deviation of 1. The PCA was calculated with VARIMAX and PROMAX rotation, which had no influence on the following results: seven principal components (PCs) were extracted, which explains about 87% of the total variance, with the first three PCs explaining about 66%. The elements with communalities of more than 0.9 after the PCs' extraction are SiO2, Al2O3, P2O5, Co, Ni, Sr, Zr, Nb, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Ho, and Hf, with P2O5, La and Pr showing the highest communalities, which means that the extracted PCs represent these variables well.

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 3 -ed.jpg

Figure 3. a) Magnesium-number Mg# versus Al2O3 and Mg# versus CaO, with Mg# = (MgO/40.32)/[(MgO/40.32+Fe2O3(t)∙0.9/79.8)] (Harvey et al. 2006). The stippled lines indicate possible groupings.

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 4 v2 -ed.jpg

Figure 4. Magnesium-number (Mg#) versus Ni. Mg# see Figure 3

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 5 v2 -ed.jpg

Figure 5. Primitive mantle-normalized trace element diagram. Primitive mantle-values taken from McDonough and Sun (1995).

 

In the following step the log-transformed data of these elements were used as variables for cluster analyses (CA) of the basalt vessels. The CAs were calculated with average linkage as cluster algorithm, combined with squared Euclidian Distance and city block distance as distance measures, as well as with the Ward-algorithm with squared Euclidean distance (Figure 6). All cluster procedures indicate that the same 36 of the 44 samples are always affiliated into one group. Seven samples do not belong to this group. However, five of these “outsiders” are affiliated into one cluster by all cluster methods. Two samples, both basanites from Figure 1, show no similarity with any of the other samples. The cluster results only disagree in sample Haz43: where the average linkage algorithm places it into the group of the large majority, the Ward algorithm places it in the “outsider” group.

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 6 v2.jpg

Figure 6. Cluster analysis results. The Tel Hazor reference group is marked with a blue frame and the vessels representing a potential second extraction site are marked with a yellow frame. The two individuals are marked in green. Haz43 is marked with a light blue ellipse.

 

Figure 7 presents a combination of the information gained from PCA and CA. The spots are coloured according to their cluster affiliation on a level of three clusters. Based on the first two principal components (“factors”, Figure 7), the dominant group is displayed as a well- constrained cluster. PCA determined P2O5, La and Pr as elements with highest communalities. A plot of the log transformed concentrations of these elements (Figure 8) shows in the three-dimensional case a confined dominant geochemical group within the vessels. In both Figures 7 and 8, sample Haz43 plots within this dominant group.

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 7 -ed_resize.jpg

Figure 7. Combination of PCA and CA results: First two principal components. The dark blue spots are the samples clustered into the dominant Tel Hazor group. The light blue spot is sample Haz43. The yellow samples possibly represent a second minor extraction site. The green samples are the basanites, which show no connection to any others.

 

4. Discussion and conclusion

Previous geochemical-mineralogical studies of basalt artefacts in the southern Levant concentrated mainly on the determination of the provenance of the artefacts, but these studies always had rather limited results due to the fact that basaltic rock extraction sites had not been identified (apart from the Late Neolithic-Early Chalcolithic extraction site at Giv’at Kipod, see Rosenberg et al. 2008; Gluhak & Rosenberg 2013; Rosenberg & Gluhak 2016; Shimelmitz & Rosenberg 2016) and that geochemical data from geological samples for comparison were, if available at all, only superficially included (e.g., Amiran & Porat 1984; Philip & Williams-Thorpe 1993; 2000; 2001; Williams-Thorpe & Thorpe 1993; Rowan 1998; Rutter 2003; Rutter et al. 2003; Watts et al. 2004; Rutter & Philip 2008).

The potential for determining the raw material variability within an assemblage of basaltic rock artefacts and its use as a baseline for determine artefact provenance seems so far underestimated. It provides important information to investigate distribution networks, even when the actual, final extraction site in the field remains (as yet) unknown. The basalt vessel workshop at Tel Hazor offers the possibility of studying a large number of samples to reconstruct the site’s role in the production and distribution of basalt vessels. The archaeological question concerning raw material variability within an assemblage of rock artefacts can be “translated” into the question of how to find a way to determine which rocks are similar to each other and which are the decisive parameters. Since a thin section study of the raw material was only possible in a few cases, we concentrate on a thorough evaluation of major and trace element data combined with multivariate methods in the present study.

 

Description: G:\0 - Journal of Lithic Studies\Issue 7 V3N3 - AGSTR carved stone\0 Gluhak etal\figures and tables\Gluhaketal Fig 8 -ed.jpg

Figure 8. Combination of PCA and CA results: The log-transformed values of La, P2O5 and Pr. Spot colours as in Figure 7.

 

The data show that the Tel Hazor workshop was mainly provided with raw material from one specific extraction site, implying a specific selection of raw material. A second, minor extraction site might have also existed. Only two of 44 samples show no connection to all other samples and come from other places. Our results thus suggest that, during the Late Bronze Age and the Iron Age, craftspeople at Hazor preferred a specific, as yet unknown, basalt source, located not in the immediate surroundings, but near a site on the Korazim block. However, this assumption has yet to be tested, and, to that end, a study of geological samples from the field is currently being undertaken. In turn, we can use the results to establish a connection between the products of the Iron Age workshop and basalt vessels found in other contexts. These results point to long-term raw material preference and access that bridged the Late Bronze and Iron Age occupation of the tell and may suggest a connection between the Bronze and Iron Age craftspeople at Hazor.

The preference for a specific basalt source is striking given the range of sources in the vicinity of Tel Hazor. These preferences, however, were probably governed by several factors. These might include the raw material properties ('quality'), transportation costs, quarry rights over specific outcrops, and others. While field data are still being analyzed to establish the location of the specific extraction site, it is already possible to use the “Tel Hazor reference group” (the characteristics of the 36 samples that represent this major extraction site) as a basis to investigate if Iron Age (as well as Late Bronze Age) basalt vessels found at other sites in the Levant were indeed produced at Hazor or if there is evidence for other workshops during this time period. These future results can help us assess what role Tel Hazor played in the production and distribution of basalt vessels during the Late Bronze and Iron Age and determine if the site was an important centre for basalt vessel production and trade or if the craftspeople working in the Area M workshop manufactured products for Hazor only.

 

Acknowledgements

The authors thank the current director of the Selz Foundation Hazor Excavations in Memory of Yigael Yadin, A. Ben-Tor, and co-director of the Hazor Excavations, the late S. Zuckerman, for permission to study the basalt vessels from Hazor. We would also like to thank supervisor of Area M, S. Bechar, for her assistance with this project. Financial support was provided by an Alumni Research and Scholarly Activity Fellowship from the University of Evansville.

 

 

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