Archaeological and Anthropological Sciences (2021) 13: 58
https://doi.org/10.1007/s12520-021-01291-7
ORIGINAL PAPER
“Come, O pilgrim”—but buy local: an isotopic investigation of animal
provisioning at Iron Age II Tel Dan
Elizabeth R. Arnold 1
&
Jonathan S. Greer 2 & David Ilan 3 & Yifat Thareani 3 & Gideon Hartman 4
Received: 17 July 2020 / Accepted: 25 January 2021 / Published online: 4 March 2021
# The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2021
Abstract
This pilot study examines the provisioning of domestic sheep and goats as it pertains to pilgrimage at the archeological site of Tel
Dan (Tell el-Qadi), Israel, an Iron Age IIA–B (ca. 10th/9th–7th c. BCE) religious center in the southern Levant traditionally
associated with Israelite Yahwistic worship. The question of how far animals were transported for sacrifice is addressed through
isotopic analyses (carbon, oxygen, and strontium) on tooth enamel of domestic sheep and goats (predominately sheep) from Iron
Age IIA–B contexts at Tel Dan through sequential intra-tooth sampling. While the results show some diversity of origins among
the animals, none was brought from a distance greater than 10–20 km from Tel Dan. As such, the data suggest that however far
pilgrims traveled to the site, the animals sold for sacrifice and consumption were raised locally.
Keywords Sacrificial practices . Sequential isotope analyses . δ13C; δ18O . 87Sr/86Sr . Israelite . Southern Levant . Sheep and
goat . Ancient Israelite religion . Ancient Near Eastern sacrifice
Introduction
The site of Tel Dan (Tell el-Qadi) in northern Israel has a long
archeological history from the Neolithic through early modern
periods (Biran 1994). Its location at the source of the perennial
* Elizabeth R. Arnold
arnoleli@gvsu.edu
Jonathan S. Greer
jonathan.greer@cornerstone.edu
David Ilan
dilan@huc.edu
Yifat Thareani
tyifat1@gmail.com
Gideon Hartman
gideon.hartman@uconn.edu
1
Grand Valley State University, 225 Lake Michigan Hall,
Allendale, MI 49401, USA
2
Grand Rapids Theological Seminary, Cornerstone University, 1001
E. Beltline Ave NE, Grand Rapids, MI 49525, USA
3
Nelson Glueck School of Biblical Archaeology, Hebrew Union
College, 13 King David St., 94101 Jeruslaem, Israel
4
Department of Anthropology, University of Connecticut, Unit 1176,
354 Mansfield Road, Storrs, CT 06269, USA
Dan spring—one of the headwaters of the Jordan River and
the largest spring in the Levant (Gil’ad and Bonne 1990)—has
long attracted inhabitants who benefited from the site’s strategic location. With an area of ca. 20 ha, Tel Dan is situated at
the crossroads of ancient routes determined by natural features
of the land (Fig. 1): a branch of the southwest-northeast international trunk route, an east-west route from the Phoenician
coast to the Syrian interior, and a north-south route running
along the Jordan and Beqa’a Valleys (Rainey and Notley
2014; Ilan 2019: 11). Imported items from the Iron Age I
(Ilan 2019: 625–627) and Iron Age II (Thareani 2015: 217–
218, 225) testify to its function as a trade node.
Archeological evidence of religious activity at the site was
indicated, even before Avraham Biran’s expedition was
launched in 1966, with the discovery of an Egyptian-style second millennium BCE figure of a goddess in a smiting pose, and
later, with fragments of Egyptian statuary discovered in excavation, in the vicinity of the spring (Biran 1994: 159–61).
Ensuing excavations of a major installation built next to the
spring in Area T (Fig. 2) suggest a possible in antis (“migdal”)
temple structure as early as the Middle Bronze Age (Ilan 2018),
and clear evidence of a massive temple complex established at
the start of the Iron Age II, if not before, that endured into the
Hellenistic and Roman periods (Biran 1994: 159–233).
The greatest concentrations of archeological materials associated with the temple complex in Area T date to the 9th and
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Archaeol Anthropol Sci (2021) 13: 58
Fig. 1 The location of Tel Dan
and a reconstruction of the ancient
roadways associated with the site.
Image courtesy of the Tel Dan
Excavations project, Hebrew
Union College, Jerusalem
8th centuries BCE. These include the remains of a monumental altar and several small altars (Biran 1994: 159–214), cultic
paraphernalia including a sacrificial “altar kit” (Greer 2010),
and more than three cubic meters of animal bone remains that
attest to the slaughter and consumption of sheep, goats, and
cattle in the temple area (Greer 2013). Integrated analyses of
textual and archeological data have associated this phase of
the precinct with Israelite Yahwistic worship (cf. Biran 1994;
Davis 2013; Greer 2013; Ackerman 2013), though others
have suggested an “Aramaean” association for the ninth century phase (Noll 1998; Arie 2008; but see Thareani 2016,
2019a, b; Greer 2013, 2017a).
Archeological evidence from the entire site suggests a
staged pilgrimage itinerary from the entrance to the city up
to the temple itself. This itinerary visited three different expansive public spaces in Areas A, M, and T (Fig. 2 and Biran
1994); at least four groups of standing stones located along the
paved processional way, in the gateways, and in the appended
plazas (Biran 1998); at least three raised platforms that
displayed focusing devices (Biran 1994: 238–241, Biran
1996, 2002; Thareani 2015); and large assemblages of
redundant artifacts—juglets in particular (Biran 1994: 255,
Fig. 214).1 Religious traditions in the Hebrew Bible associate
the site with Israelite Yahwistic worship (Judges 17–18; 1 Kgs
12:28–33; Amos 8:14), and specifically as a pilgrimage destination following the installation of one of two golden calves
there by Jeroboam I (1 Kgs 12:28–33; see Na'aman 1999 with
references). An essential characteristic of the religious experience of “pilgrimage” is that the pilgrim must endure hardship
on his or her journey, and that this hardship is part of the
sanctifying nature of the experience (e.g., Coleman and
Elsner 1995; Turner and Turner 1978; Winkelman and
Dubisch 2005: xxiv, xxx). As pilgrimages often involve animal sacrifice at the final destination, we ask whether the live
animals themselves were subject to the arduous journey,
alongside their owners, or if the animals were purchased or
provided on site prior to being offered up and consumed in
festive meals. Is there evidence of pilgrims bringing their animals with them from long distances for slaughter? And, if so,
1
The archeological manifestation of the pilgrimage itinerary is to be the subject of a forthcoming publication.
Archaeol Anthropol Sci (2021) 13: 58
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58
Fig. 2 A site plan of Tel Dan with its excavated areas. Courtesy of the Tel Dan Excavations project, Hebrew Union College, Jerusalem. Material
analyzed from Area M (communal area) and Area T (temple area)
from how far away do these pilgrims travel with their animals?
To begin to answer these questions, one must examine patterns of animal mobility, where the animals are coming from,
how the landscape is utilized, and how animals are distributed
within an urban setting.
This question is addressed through a pilot isotopic study of
targeted samples of domestic ovicaprinae from Area M, supplemented by exploratory sampling of Area T, from Iron Age
IIA–B contexts (ca. 1000/900–700 BCE)2 associated with
Israelite (and perhaps “Aramaean”)3 worship at the site.
Stable (carbon, oxygen) and radiogenic (strontium) isotope
analyses are utilized to examine the nature of the associated
temple/domestic provisioning patterns, particularly as they
pertain to the scope and the extent of mobility of domestic
animals. We hypothesize that sheep and goats raised and
culled in the immediate vicinity of the site would show local
2
The beginning of the Iron Age IIA in the southern Levant is a matter of
debate; see the discussion in Finkelstein and Mazar (ed. Schmidt) 2007, for an
introduction to the issues.
3
By “Aramaean,” we refer to various groups with Syro-Mesopotamian ethnic
orientation. On problems associated with the term and definitions, see
Younger 2016.
isotopic signatures while animals imported for sacrifice, or
those accompanying pilgrims over long distances (i.e., those
at a greater distance than 1 day’s walk), would show more
diverse and non-local signatures (Sheridan and Gregoricka
2015). Since the religious traditions in the Hebrew Bible associate this site with Israelite Yahwistic worship and pilgrimage, and other biblical texts allow for the provision of locally
raised animals for sacrifice, we hypothesize that the samples
will exhibit isotopic signatures from nearby grazing regions
rather than from great distances.
The application of isotope analysis
to archaeology
Stable isotope analysis has been applied to an ever-increasing
range of archeological questions. In early research, isotopic
values for animal remains were calculated only as an intermediate step in the analysis of human dietary patterns
(Katzenberg 1989; van der Merwe et al. 2000). Today, the
research focus is directed at the animal isotopic values
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themselves (e.g., Mashkour et al. 2004; Balasse et al. 2001,
2003). Stable isotope analyses are well established as a method for determining animal diet (DeNiro and Epstein 1978,
1981), reconstructing environments (Schoeninger et al.
2000), and inferring methods of herd management (Balasse
et al. 2003; Makarewicz and Tuross 2006, 2012). Moreover,
the mobility, trade, and exchange of animals within economic
systems can be discussed (Arnold et al. 2016, 2018; Ezzo et al.
1997; Grupe et al. 1997; Hodell et al. 2004; Price et al. 1994,
2000). Stable isotope analyses can provide data on the animals’ diet and the environmental conditions in which they
were raised, without the need for direct or continual observation and documentation throughout the animals’ lives (Balasse
et al. 2003; Bentley et al. 2004; Bocherens et al. 2001;
Gadbury et al. 2000; Makarewicz et al. 2016; Price et al.
2000; Sealy et al. 1995; Sharp and Cerling 1998). Isotopic
ratios are incorporated into animal tissues and are stored for
variable periods of time, depending on the turnover rate of the
different tissues. As tooth enamel does not turn over once
formed (Hillson 2005), isotopic analysis provides a picture
of the animal’s diet, and/or mobility at the time of formation.
For domestic animals, these are factors that are controlled by
the herders and/or producers.
Methods and materials
Eleven lower molar teeth from different individuals were analyzed in this pilot study. The individuals were isolated from
the larger collection based on find spots associated with homogeneous Iron Age II ceramic assemblages and clearly defined archeological contexts, specifically from floors and their
associated debris (Table 1). All specimens were clearly identified as domestic animals. All samples are sheep (Ovis aries)
with the exception of OC#10 which is identified as a goat
(Capra hircus). Teeth were identified by species according
to morphological criteria (Payne 1985; Halstead et al. 2002;
Balasse and Ambrose 2005; Zeder and Pilaar 2010). The samples were selected from fully erupted M1, M2, and M3 molars
based on their structural integrity and suitability for sampling
required for isotope analysis.
The sampled animals were drawn primarily from secure
and clean Iron Age II contexts in Area M, which overlay a
broad, paved, open square that we interpret as a space for
communal ritual and commercial gatherings associated
with the temple (Stratum II). The square was subsequently
superseded by domestic structures (Stratum I). Two tooth
samples (OC#10 and OC#11) were taken from contexts
associated with the temple complex in Area T, though the
stratigraphy and chronology of the area are not yet finalized. Sheep and goat from Area T were included to give an
initial indication of any potential differences between the
two areas, with the combined results establishing a
Archaeol Anthropol Sci (2021) 13: 58
framework for testing future samples once contexts are
clarified in further excavation and analysis.
The teeth analyzed in this pilot study were thoroughly
cleaned and a series of horizontal 1 mm wide bands were
drilled from bottom to top and parallel to the growth and
mineralization axes of the tooth at 1.0 mm intervals, following
the methods outlined by Bocherens et al. (2001). The number
of samples was dependent on the size of each tooth and varies
from three samples (on a worn M1) to 24 samples.
The timing of enamel mineralization and isotope signature
integration is a key consideration for accurate time resolution
for micro sampling along animal teeth (Wiedemann et al.
1999; Balasse 2002; Passey and Cerling 2002). For sheep
and goat, the first permanent molar is half formed at birth
and is complete by 9 months of age and will have a minimal
maternal suckling signal (Balasse 2002). The formation of the
third permanent molar begins at 1 year of age (Hillson 2005).
A 5-to 6-month delay between tooth mineralization and the
tooth’s isotopic record has been documented (Balasse et al.
2012). As such, the signal provided starts in the second year of
life. Several researchers (e.g., Meiggs 2007; Montgomery
et al. 2010) have highlighted similar issues in strontium isotopes. Strontium is incorporated into the tooth over a 12month period such that the timing of isotopic changes in the
light isotopes (C and O) might not be synchronous with the
radiogenic strontium.
Two first molars were sampled (OC#4 and OC#7) and
represent the isotopic signal of these individuals during uterine life. However, these teeth were well worn (Stage G—4–
6 years, Payne 1973) and represent adult animals while their
isotopic signatures provide a glimpse of the diet of their mother and their early life. While these teeth provide only a partial
isotopic sequence (represented by only 3–5 sequential samples along the tooth), the known maternal influence on the first
molar allows a tentative glimpse of more than one generation
of the herd management pattern. The majority of the teeth
sampled were third molars providing isotopic signals from
the individuals’ first year of age onwards.
Pretreatment of the samples followed the methods of
Balasse (2002). Tooth enamel was treated with a 2.5%
NaOCl (sodium hypochlorite) solution overnight to remove
organics and then rinsed five times with distilled water and
treated with 0.1 M CH3COOH (acetic acid, pH 3) for 4 h to
remove diagenetic carbonates. The samples were then rinsed
five times with distilled water and freeze dried. Even numbered samples were analyzed for strontium isotope composition and odd numbered samples were analyzed for carbon and
oxygen isotope compositions. Carbon and oxygen isotopic
analyses were performed at the Anthropology Department
Stable Isotope Laboratory and Mass Spectrometry
Laboratory of the University of Illinois Urbana-Champaign
where ~700 μg of the prepared sample was weighed into
individual vessels and reacted with 100% phosphoric acid
Archaeol Anthropol Sci (2021) 13: 58
Table 1
Page 5 of 14
58
Archeological association of samples (*Area T stratigraphy is not final)
Sample Tooth sampled Locus Basket Context Summary
Phase
Stratum Date
OC#1
Ovis
Right M3
8307
M2
Ib
End of eighth–seventh
century BCE
OC#2
Ovis
Right M3
8326
M3
IIa
OC#3
Ovis
Left M3
8324
21,234 Tamped earth surface with pottery, bones,
and tabun material (levels: 198.9–198.24).
M3
IIa
First half of the eighth
century BCE, destroyed
in 732 BCE
First half of the eighth
century BCE, destroyed
in 732 BCE
OC#4
Ovis
Right M1
8161
M3-M2 IIa-Ib
First half of the eighth–seventh
century BCE
OC#5
Ovis
Left M3
8325
M3
IIa
First half of the eighth century
BCE, destroyed in 732 BCE
OC#6
Ovis
Left M3
8080
M2
Ib
End of eighth–seventh
century BCE
OC#7
Ovis
Left M1
8139
M3
IIa
First half of the eighth century
BCE, destroyed in 732 BCE
OC#8
Ovis
OC#9
Ovis
Left M3
8326
M3
IIa
Left M3
8134
M1
Ia
First half of the eighth century
BCE, destroyed in 732 BCE
Late seventh–early sixth
century BCE
OC#10 Left M3
Capra
OC#11 Left M3
Ovis
2383
20,534 Pavement in the northeast sloping towards
the east, perhaps as a topographical
adjustment, with a small limestone floor
below (level: 198.75 m) superimposed
by a tamped brown fill mixed with plaster
remains. Pottery and many bones associated
with the floor (level: 198.75 m), as well as
worked bones, iron pieces, and the remains
of a furnace. The floor is higher in the west
and abuts W4653.
31,217 Fallen debris over and in a bin at the corner of
W4107 and W4111, including yellow
decomposed brick material
(levels: 198.77–198.27 m).
20,193 Brown soil with gravel at the center at the
head of W4510 (level: 198.85 m), containing
a bead (level: 198.63 m).
20,436 A 30–40 cm fill below the layer of L8136
containing vessels and atop the pavement
of L8135. The pavement continues below
the northern balk and is damaged at its eastern
and northwestern parts (levels: 199.59–199.22 m).
21,337 Fill superimposing a surface with large storage
jar fragments (level: 198.66 m)
20,417 Large pavement surface with vessels and
sherds (levels: 200.05–199.93 m) that was
disturbed at the south. The pavement abuts
W4610 at the west.
12,626 Occupational debris and mudbrick collapse
above tamped earth floor (level: 198.10 m).
12,097 Occupational debris and mudbrick collapse
above pavement (level: 197.16 m).
T*
II
T*
III
2305
21,192 Cobble-paved alley between structures,
with evidence of two re-pavings and
scattered tabun material. The area slopes
from east to west (levels: 199.85–199.33 m).
21,217 Fill superimposing a surface with large
storage jar fragments (levels: 198.8–198.36 m).
(H3PO4) at 70 °C in an automated Kiel III carbonate device in
which CO2 is liberated from enamel, cryogenically distilled,
and subsequently flowed to a Finnigan MAT 252 isotopic
ratio mass spectrometer. Two laboratory standards (NBS18 5.00‰ δ13C and -23.00‰ δ18O and NBS 19 +1.95‰ δ13C
and -2.20‰ δ18O) were interspersed and replicates are applied
to ensure accuracy. Analytical precision is typically ±0.07‰
for δ13C and ± 0.14‰ for δ18O.
Strontium isotope measurements were performed on a Nu
Plasma HR multi-collector inductively-coupled plasma mass
spectrometer (MC-ICP-MS) at the University of Illinois,
Urbana-Champaign Geology Department. Tooth enamel
First half of the eighth century
BCE, destroyed in 732 BCE
First half of the eighth century
BCE, destroyed in 732 BCE
samples (pretreated following the methods of Balasse 2002
discussed above) were dissolved in 0.5 ml of 3N nitric acid
(HNO3) under clean lab conditions. Cation exchange columns
loaded with Eichrom® Sr spec resin and pre-conditioned with
3N HNO3 were prepared and the 0.5 ml samples were then
loaded. Column blanks consisted of 0.5 ml of 3N HNO3.
Columns were washed four times with 0.3 ml of 3N HNO3
and then strontium was eluted into 4 ml Teflon® vials with
1 ml of 0.05 N HNO3 and 3 ml of ultrapure deionized water
(Milli-Q, Millipore) following Horwitz et al. (1992). Sample
concentrations are measured and corrected to optimal range.
Linear normalization of sample results was applied based on
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Archaeol Anthropol Sci (2021) 13: 58
within-run trends in SRM 987 (standards are run every eight
interval) relative to its accepted value (0.710255). Analytical
precision on repeated standard measurements was ±0.00003.
Results
Isotope results are presented in Supplementary Tables 1 and 2.
Isotope results are presented in Figs. 3 and 4. Descriptive
statistics are presented in Table 2.
Two first molars were sampled (OC#4 and OC#7), sampling the oldest part of the tooth closest to the root/enamel
junction (REJ); they represent the isotopic signal of these individuals during the first months of life. The majority of the
teeth sampled were third molars providing isotopic signals
from individuals’ first year of age onwards. There are no notable distinctions between these early and later life phases in
the isotope data.
Oxygen isotope values range from −4.1 to 5.0‰ suggesting a wide range of oxygen isotope values across the sample.
However, intra-tooth variation is much lower, ranging from
0.6 (OC#4) to 5.6‰ (OC#8). Two individuals show the same
range of variation of 4.4‰ across the tooth (OC#2 and
OC#11).
The range of variation of strontium values is low overall in
all individuals. OC#9 has the lowest range of 0.00004 and
OC#6 has the highest: 0.00099. Few individuals show intratooth variability in the strontium isotope values, except for
specimens OC#6 and OC#11.
Carbon isotope values range from −13.0 to −6.9‰ for all
caprines sampled. Again, the range of variation for each animal is lower, with a maximum of 3.3‰ in OC#2 and a minimum of 0.1‰ in OC#4 (although limited by only two
Table 2
samples along this short M1). Three individuals show the
same range of variation of 1.1‰ across the tooth (OC#5, 7,
and 8). The carbon isotope results indicate that the caprine diet
contained predominantly C3 vegetation that dominates the
Mediterranean climate with a variable inclusion of C4 vegetation in the diet.
Discussion
Reconstruction of herding and animal trade at the Iron Age
site of Tel Dan requires an understanding of the environmental
factors contributing to the isotopic composition of the local
biome. The site of Tel Dan is located at the northern boundary
of the upper Jordan Valley (UJV, aka the Hula Basin), part of
the Great Rift Valley. The UJV is bordered on the west by the
Upper Galilee Mountains that rise up to over 1000 m asl.
These mountains are composed of Cretaceous and Neogene
marine sedimentary rocks. To the northeast lies Mt. Hermon
(Fig. 1), a Jurassic marine sedimentary massif that rises to
elevations of more than 2700 m asl. The eastern zone of the
UJV is the Golan Heights, composed of successive layers of
volcanic bedrock dating from the Pliocene to the late
Pleistocene, reaching an altitude of over 1000 m asl (Sneh
and Weinberger 2014). Mean annual temperatures in the
UJV are higher than the surrounding mountains (maximum
annual average in UJV = 26.6 °C; in Zefat, Upper Galilee =
20.7 °C). Monthly precipitation is limited to the cool season
(November–April), typical of the Mediterranean climate, and
increases with altitude. Summers are uniformly hot and dry.
Mean annual precipitation in the UJV is approximately
500 mm/year while in the surrounding mountains it varies
Descriptive statistics
87
Sr/86Sr
δ13C
Caprine n x
2σ
OC#1
OC#2
OC#3
OC#4
OC#5
OC#6
OC#7
OC#8
OC#9
OC#10
OC#11
0.0001 0.7081 0.7081 0.0001
0.0000 0.7082 0.7084 0.0002
0.0003 0.7059 0.7063 0.0004
6
6
6
1
5
4
3
5
2
5
4
0.7081
0.7083
0.7060
0.7051
0.7078
0.7071
0.7082
0.7078
0.7083
0.7084
0.7079
0.0001
0.0009
0.0001
0.0001
min
0.7077
0.7057
0.7082
0.7078
max
0.7078
0.7067
0.7083
0.7079
∆minmax
0.0001
0.0010
0.0001
0.0001
0.0002 0.7082 0.7084 0.0002
0.0004 0.7076 0.7080 0.0004
δ18O
n x
σ
6
6
5
2
5
4
2
5
3
4
5
1.1 −9.8 −7.2 2.6
1.3 −10.2 −6.9 3.3
0.8 −13.0 −11.1 1.9
−8.5
−8.6
−11.9
−10.7
−8.8
−11.3
−10.7
−8.6
−10.5
−11.5
−10.3
min
max
∆minmax
0.5 −9.6 −8.5 1.2
1.2 −12.8 −10.0 2.9
0.5
1.4
1.1
0.7
−9.0
−11.8
−12.7
−11.3
−7.9
−9.0
−10.5
−9.6
1.1
2.8
2.2
1.7
min
max
x
σ
2.8
2.9
−1.8
−2.8
−2.2
−1.2
1.7
1.2
0.8
1.2
−1.6
0.9 2.0
4.5
2.5
1.6 0.7
5.1
4.3
1.7 −3.8 −0.2 3.6
∆minmax
1.7 −4.1 −0.2 3.9
1.6 −2.6 1.1
3.7
2.1
1.6
2.1
1.7
−2.2
−1.0
−1.4
−3.1
3.4
2.2
3.6
1.3
5.5
3.2
5.0
4.4
Archaeol Anthropol Sci (2021) 13: 58
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58
Fig. 3 Isotopic results from sheep
and goat from Area M. Individual
sample numbers are noted in the
top left corner of each graph.
Oxygen in orange, carbon in blue,
and strontium in red
between 700 and >1000 mm/year (http://www.ims.gov.il/
IMSEng/CLIMATE).
Regional variability in the bioavailable strontium isotope
(87Sr/86Sr) ratio results in a clear separation between potential
Fig. 4 Isotopic results from sheep
and goats from Area T. Individual
sample numbers are noted in the
top left corner of each graph.
Oxygen in orange, carbon in blue,
and strontium in red
pastures that could have provisioned Tel Dan (Fig. 5; for
comprehensive background see Hartman and Richards
2014). The region can be divided into eastern and western
zones of the UJV. In the west, high altitude rocks are hard
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Archaeol Anthropol Sci (2021) 13: 58
Western Zone
Eastern Zone
Golan
Galilee
1000
750
500
UJV
250
0
0.7073±0.0006
1
6
0.7086±0.0003
0.7080
0.7086±0.0003
0.7058±0.0005
ABM
0.7076
Tel Dan
0.7076
3
5
0.7073±0.0006
4
0.7047±0.0002 - 0.7058±0.0005
2
0.7079 - 0.7083
N
5 Km
Fig. 5 Geological map of the northern region of the UJV (Upper Jordan
Valley) and its surrounding lithic units (Sneh and Weinberger 2014). The
lithic units are partitioned by dotted black lines; each polygon is assigned
distinct plant-based bioavailable 87Sr/86Sr ratio/s (data from Hartman and
Richards 2014). For basalt ages see Mor 1993. The blue-framed 87Sr/86Sr
ratios are taken from Spiro et al. (2011) and represent measurements of
local spring water. Color codes: Jurassic (blue); Cretaceous (green);
Neogene (orange/yellow); basalts (red). The section at top, above the
geological map, represents the altitude profile (Google Earth Pro). The
region is divided into western (87Sr/86Sr ≥ 0.7079) and eastern zones
above the UJV (87Sr/86Sr ≤ 0.7079); the western zone includes the
Cretaceous and Neogene lithic formations; and the rest is assigned to
the eastern zone.
Cretaceous limestones and dolomites upon which “terra
rossa” (USDA: Rhodoxeralfs) soil develops (Fig. 5 #1),
(Singer 2007). The lower Galilee slopes are dominated by soft
Cretaceous and Neogene rocks upon which “rendzina” soils
develop (Fig. 5 #2), (Dan et al. 1972). Bioavailable 87Sr/86Sr
ratios measured in plants are mostly radiogenic in terra-rossa
soils (0.7086) but are typically equal or higher than 0.7079 in
rendzina soils (Hartman and Richards 2014). The eastern zone
is dominated by successive volcanic layers of basalt and
pyroclasts, the oldest and westernmost are dated to the upper
Pliocene (Dalwe flow, 0.7077) and Pleistocene (Hasbani flow,
0.7063, Fig. 5 #3). The lithic units higher up and further to the
east date to the mid-Pleistocene (Muweisse flow, 0.7063, Fig.
5 #4), and the youngest, uppermost units date to the latePleistocene (Sa’ar flow, 0.7040, Fig. 5 #5; Mor 1993;
Hartman and Richards 2014). Finally, in the northeast, the
Mt. Hermon massif is composed of Jurassic limestone upon
which terra-rossa soil develops. It is expected to have a typical
87
Sr/86Sr ratio of ~0.7086 (Fig. 5 #6) resulting from atmospheric deposition rather than from local bedrock weathering
(Hartman and Richards 2014). Analysis of spring waters indicates direct weathering and dissolution of host bedrock
(Starinsky et al. 1980) and the UJV spring water is no
exception. The dissolved strontium in the Banias spring water,
which derives from the Mt. Hermon Jurassic unit, has an
87
Sr/86Sr ratio of 0.7072 (Spiro et al. 2011). The concentrations of strontium in water are orders of magnitude lower than
those in vegetation, such that plants are better proxies for
measured herbivore 87Sr/86Sr ratios (Bentley 2006; Hartman
and Richards 2014). Nonetheless, given the absence of indigenous plant samples from the heavily cultivated UJV region,
water samples are used to provide a rough proxy for local
87
Sr/86Sr ratios.
Environmental oxygen isotope (δ18O) values are determined
by the composition of precipitation, mostly in the form of rainfall.
The amount of precipitation is a primary factor that controls
water oxygen isotope values in the southern Levant (Ayalon
et al. 2004). Altitude is another factor that has been shown to
provide a reliable proxy for carbonate oxygen in gazelle tooth
enamel (Hartman et al. 2015); the isotopic values of meteoric and
ground water are both correlated linearly with altitude (Gat and
Dansgaard 1972; Ayalon et al. 2004; Dafny et al. 2006; Hartman
et al. 2015). Secondary 18O enrichment in herbivore tooth enamel at low altitudes results from plant and surface water evapotranspiration during the dry season (Gat and Dansgaard 1972).
The large altitudinal gradient between the UJV and its
Archaeol Anthropol Sci (2021) 13: 58
Page 9 of 14
surrounding mountains provides a clear indication of herding
elevation. The lowest δ18O value measured in the teeth that represent wet season enamel formation should reflect the composition of environmental water least affected by evapotranspiration.
It therefore serves as trustable proxy of altitude (Hartman et al.
2015). The highest δ18O values reflect increases in evapotranspiration during the dry season and are not, therefore, considered
an altitude proxy.
Carbon isotope (δ13C) values provide a complementary
proxy for the type of vegetation available for herded animals.
While the local Mediterranean flora is dominated by C3 vegetation (Winter and Troughton 1978; Hartman and Danin
2010), C4 vegetation of the Cyperaceae (sedge) family prevails in the abundant springs and ponds of the UJV (Danin
2004). Otherwise, incorporation of C4 vegetation into the diet
can take place in south facing slopes where edaphic conditions
select for plant species that can tolerate high solar radiation
and growth under conditions of limited water availability
(Pavlíček et al. 2003). With regard to the dominant local C3
vegetation, water availability—resulting from the amount of
precipitation and soil conditions—affects the degree of isotopic discrimination (Δ13C, Hartman and Danin 2010). Thus,
two contrasting situations exist where elevated δ13C values
can be measured in the teeth: consumption of water-dipped
sedges in UJV, or of water-stressed vegetation on the surrounding hills. These can be easily differentiated: the former
will be associated with negative δ18O values, reflecting the
unlimited water conditions available to the vegetation and,
thus, the animals; the latter will be associated with arid conditions and positive δ18O values.
The amplitude of seasonal variability and the number of
samples per tooth are not correlated. This big seasonal variability is reflected in the small number of samples (3) as much
as it is reflected in the large number of samples per tooth (>5),
(see Supplementary Fig. 1).
Carbon isotope values indicate that the animal diet
contained predominantly C3 vegetation which dominates the
Mediterranean climate. The teeth can be divided roughly into
two groups based on their 87Sr/86Sr ratios (Fig. 6): the western
zone (WZ) animals (#1,2,7,9,10), and the eastern zone (EZ)
animals (#3,4,5,6,8,11) (87Sr/86Sr WZ x = 0.70825 ± 0.00009;
EZ x = 0.70682 ± 0.00012; t-test assuming equal variance
P < 0.05). A summary of the results is provided in Table 2.
None of the 87Sr/86Sr ratios measured in the Tel Dan sheep
and goat teeth shows consumption of vegetation that comes
from terra rossa soils (0.7086), and therefore there is no evidence for animals pastured in the WZ Upper Galilee or Mt.
Hermon (Fig. 5, regions #1 or #6). While OC#10 has a mean
isotope ratio of 0.7084 (+ 0.0002) that may fall within the
range for terra rossa soils, when δ18O values of OC#10 are
also considered, this high altitude area of the Western Zone
can be disregarded. A combined bivariate plotting of δ18O
values and 87Sr/86Sr ratios shows good agreement between
the two variables (Fig. 6).
WZ individuals—defined as such based on their 87Sr/86Sr
ratio which positions them in rendzina soils—are associated
with positive δ18O values. These pastures are found at the low
altitudes of the Galilee foothills. Comparison of the δ18O
values of WZ and EZ animals shows striking differences
(Fig. 7; WZx = 1.88 ± 0.95; EZx = −1.39 ± 1.39; t-test assuming equal variance P < 0.005). While negative, EZ δ18O
values are more variable; the teeth of animals originating in
the Golan Heights have the lowest δ18O values and the least
radiogenic 87Sr/86Sr ratios. These 87Sr/86Sr ratios are measured in mid-altitude vegetation growing on soils formed
above Mid- and Late-Pleistocene basalts (Fig. 6 #3,4,6). The
wide range of EZ animals δ18O values also provides evidence
for low altitude herding of sheep and goat in locations that
coincide with more radiogenic 87Sr/86Sr ratios (#5,8,11).
These can be found in closer proximity to Tel Dan.
When mean δ18O and δ13C values of each tooth are
regressed, they show a positive correlation when EZ and
WZ sheep and goat are considered separately (Fig. 7).
When both regions are combined, there is a significant
difference in δ13C values between animals showing minor
consumption of a C4 diet compared to those who subsist exclusively on C3 vegetation (exclusive C3 diet x = −10.99 ±
0.60‰; incorporated C 4 diet x = −8.56 ± 0.01‰; t-test
86
Sr/ Sr
Altitude
87
Fig. 6 Bivariate plot of Tel Dan
mean87Sr/86Sr ratios and δ18O
values measured in individual
molar teeth. Black-filled circles
represent animals assigned to
western zone origins; white-filled
circles represent animals assigned
to eastern zone origins. Colors
and numbers reflect lithic units
and locations showing on Fig. 5
58
0.7090
0.7085
0.7080
0.7075
0.7070
0.7065
0.7060
0.7055
0.7050
0.7045
High
Low
1
2
5 3
9 10 7
8
2
1
Western Zone
6
3
Eastern Zone
3
4
4
y = -0.0001x2 + 0.0004x + 0.708
R² = 0.649
5
-6.0
-4.0
-2.0
0.0
2.0
18
δ O (‰, VPDB)
4.0
6.0
58 Page 10 of 14
-7
C4
P <0.05
13
δ C (‰, VPDB)
-8
8
5
-9
y = 0.64x - 9.78
R² = 0.55, P=0.15
-10
11
9
4
-11
1 2
7
C3
-12
P<0.0005
Fig. 7 Regressions of mean δ18O
and δ13C values, east zone (white
circles, excluding #5 in gray) vs.
west zone (black circles) showing
the positive correlation between
C4 plant consumption and δ18O
values
Archaeol Anthropol Sci (2021) 13: 58
6
10
y = 1.24x - 12.28
R² = 0.78, P=0.05
3
-13
-5.0 -4.0 -3.0 -2.0 -1.0
0.0
1.0
2.0
3.0
4.0
5.0
δ18O (‰, VPDB)
assuming equal variance P < 0.0005). The same test on differences in δ18O values between individuals feeding exclusively
on C3 vegetation compared to those who incorporated C4
vegetation into their diet shows that C4 incorporation into diet
is associated with low topographies, and more evaporative
conditions (exclusive C3 diet x = −0.53 ± 1.73‰; incorporated
C4 diet x = 2.31 ± 0.95‰; P < 0.05). It is expected that in hot
and arid locations arid-adapted, open habitat C4 species will
increase their presence in the landscape, contributing to domestic animal diet. One EZ sheep (#5) showing the incorporation of C4 vegetation into its diet has exceptionally low δ18O
values (−2.2 ± 1.7‰). In this exceptional case, it is hypothesized that the sheep foraged along permanent water bodies that
are common in the UJV and supplemented its diet with wet
habitat sedges. Permanent water bodies enjoy annual replenishment by groundwater with negative δ18O values.
The strontium, carbon, and oxygen data together suggest
that the animals grazed within the local region; all approximately within a day’s walk of the site. Though the number of
animals utilized for this pilot study is modest (n = 11), this
initial analysis supports the hypothesis that animals consumed
during the eating events in the large open space of public
display (Area M) were locally sourced. In addition, there is
minimal evidence for seasonal mobility patterns.
However, the diversity of the samples from the public area
was greater than expected. While EZ sheep (n = 6) were
herded in the immediate vicinity of the tel, two further distinctions can be made within this group. Three individuals (#3, 4,
6) with comparatively lower δ18O values and lower 87Sr/86Sr
ratios were pastured in the Golan Heights. Others (#5, 8, and
11) were herded in closer proximity to the site, demonstrated
by a more radiogenic 87Sr/86Sr ratio. As the majority of the
sample is sheep, the variation is not due to the different feeding behaviors of sheep vs. goats. WZ individuals (n = 5) were
imported from the Galilee foothills, perhaps within the
political boundaries of other cities (Tel Abel Beth Ma‘acah
and Tel Hazor). While the predominance of sheep is unusual
in the region, recent zooarchaeological analyses at Tel Hazor
have identified a sheep-dominated industry, atypical for the
region (Marom et al. 2014). Ongoing isotope research at Tel
Dan is expanding the sample size and focusing specifically on
additional goat samples.
Regarding the animals from the temple area (Area T), one
(#11) was herded in close proximity to the site. But this is not
a unique signature since other animals with these same origins
were recovered from the paved public space in Area M. The
other animal from Area T (#10, the single goat) comes from
further away (WZ Galilee foothills).
While the strontium isotope values measured in the teeth of
specimens OC#6 and OC#11 may be considered to vary
enough to suggest seasonal mobility of herds, the site is situated within a pronounced wet and dry seasonal Mediterranean
climate regime. The Tel Dan region (Upper Jordan Valley,
Golan, Upper Galilee) does not suffer from a seasonal shortage of green vegetation (Danin 2004) or a lack of water supply
(Sade et al. 2016) that would necessitate pronounced seasonal
mobility of herds. The individual seasonal movement of each
caprine, as reflected in intra-tooth 87Sr/86Sr variability is limited, further suggesting localized herding (Figs. 3-4).
The separation of Tel Dan caprines into either WZ or EZ
origins reveals that the former were slaughtered at older ages
than caprines raised in the EZ of the UJV (molar crown height
WZ = 23.28 ± 8.28 mm, EZ = 26.48 ± 11.03 mm, excluding
#4 EZ = 30.95 ± 1.51 mm, one tail t-test P < 0.05) (Fig. 8).
This observation is based on the height of tooth crowns, which
has implications for the type of animal product exploitation
(dairy/wool vs. meat). This observation, supported by the
zooarchaeological analysis of the larger assemblage (Greer
2013), may suggest different management strategies and exploitation strategies of these spatially separated herds, though
Archaeol Anthropol Sci (2021) 13: 58
Page 11 of 14
58
Fig. 8 Plot of serially sampled individual caprine teeth: a. western zone;
b. eastern zone of the UJV tooth enamel carbonate δ18O and δ13C values.
Black dashed lines are group mean polynomial regression lines formed
between isotope values and location relative to tooth cervix. Red dashed
lines mark maximum crown height (age) of western zone caprines relative
to the eastern zone caprines
our sample size prohibits any definitive conclusion. With larger samples, production strategies—whether the domestic animals were utilized for meat or for secondary products, such as
milk, traction, wool or hair—will be reflected in the animals’
age at death (Payne 1973; Hesse 1982; Greenfield 1988, 2010;
Greenfield and Arnold 2015; Vila and Helmer 2014). As such,
interpretations on secondary product use from this analysis are
only tentative.
we interpret as a place for communal rituals and commercial
gatherings associated with the temple that later shows evidence of domestic structures at Iron Age II A–B (ca.
10th/9th–7th c. BCE) Tel Dan—were locally sourced. The
exploratory sampling from the temple complex in Area T also
suggests locally sourced animals within these parameters and
exhibits no significant difference from Area M. This pattern is
supported by biblical texts concerning the provisioning of
animals for pilgrims (though dating biblical texts and
traditions that pertain to Israelite sacrifice is a complicated
matter; see Greer forthcoming). For example, Deuteronomy
14:24–26 allows the use of local animals for sacrifice by pilgrims traveling long distances, and in Leviticus 22:17–25, we
find a prohibition of foreign animals with suspected abnormalities for sacrifice relayed among a list of circumstances that
render an offering “blemished” (cf. Greer 2017b).
While such a proposal may not conform to the idea of an
arduous pilgrimage with regard to sacrificial provisioning, it does
fit in terms of practicality: animals were readily available for
purchase by incoming pilgrims. Their availability would have
created a flourishing branch of the local economy, which resonates with biblical provisions for purchasing local animals (Deut
14:24–26). Furthermore, a local provisioning system for pilgrims
would have allowed for quality control of the animals, especially
important for the local cultic officials given the multi-ethnic nature of the region’s population and a desire to maintain the purity
of the sacrificial victim (cf. Lev 22:17–25). Local provisioning
would also facilitate access to younger animals. EZ animals are
both younger and closer to the site than WZ animals. This is
Conclusions
The capacity to pinpoint the origins of sheep and goat and to
determine the consumption of arid-adapted vs. humid/wet C4
plants has been demonstrated, allowing for the application of
our results to an analysis of the broader economy of the site.
The isotopic results suggest that irrigated agriculture (orchard
crops, vegetables) benefited the residents of Tel Dan and
outcompeted herding. Domestic herds were pushed to less
desirable locations or imported to the city from neighboring
settlements. Marom et al. (2009) argue that the animal component of the economic system was managed separately from
the agricultural component throughout western Asia in antiquity. Sheep and goats were ranged extensively and at a distance from settlements to reduce the impact on agricultural
production during the growing season (Hesse 1986; KöhlerRollefson 1992; Redding 1981).
We have demonstrated that the animals represented in the
samples we analyzed from Area M—a paved, open space that
58 Page 12 of 14
preferable in general, in that immature animals could not travel
without their mothers prior to weaning, and they were required
for specific offerings in the biblical text. In fact, a preference for
younger animals has already been observed in previous analyses
of faunal remains from the temple complex (Wapnish and Hesse
1991; Greer 2013). Together, these elements of the proposed
pilgrimage model dovetail with the highly localized nature of
the entire foodway chaîne opératoire—slaughtering, butchering,
eating, and disposing—reconstructed from archeological remains
of the temple feasts (Greer 2013: 92–93).
The different mortality patterns observed here plotted against
the backdrop of studies with larger sample sizes may suggest that
animals imported from the Galilee foothills (WZ) were exploited
heavily for secondary products. This may be another reason for
the import of animals from the surrounding area to Tel Dan, aside
from any cultic connotations. Milk is unlikely to be the key product for this exchange as dairy herds would need to be maintained
in close proximity to the site (cf. Wapnish and Hesse 1988). This
specialized pastoral economy may have served as a means of
regional integration (Zeder 1991; Wapnish and Hesse 1988). A
similar strategy is reflected in the Hula Valley during the late
nineteenth–early twentieth centuries CE when the area was subjected to the dominance of local pastoral groups (Thareani
2019b). In general, the export or import of domestic stock is
considered evidence of increasing economic specialization since
a network of exchange would be necessary to integrate communities that specialize in production (Wapnish and Hesse 1988).
This “hyper-locality” of the animal provisioning at Tel Dan
would therefore seem to be directly related to its status as a
pilgrimage city. Requirements for locally sourced animals fed
the local economy of the Danites while ensuring access to
quality-assured sacrificial animals for incoming pilgrims.
Cult was commercialized and commerce was ritualized.
Supplementary Information The online version contains supplementary
material available at https://doi.org/10.1007/s12520-021-01291-7.
Acknowledgements We wish to express our appreciation to the Grand
Valley State University and Cornerstone University, Grand Rapids
Theological Seminary, Arlyn and Marcia Lanting, and Stephen
Disselkoen for their generous support of the Tel Dan excavations and
the Hesse Memorial Archeological Laboratory. We are grateful to
Stanley H. Ambrose and Shari Fanta, Tom Johnson, Craig Lundstrom,
and Gideon Bartov for lab access and assistance with technical issues at
the University of Illinois (Urbana-Champaign). Thank you to Dov
Porotzky for producing the general plan of site (Fig. 2) and the plans of
Area M.
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