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Journal of Archaeological Science: Reports 3 (2015) 237–246
Contents lists available at ScienceDirect
Journal of Archaeological Science: Reports
j ourna l homepage: ht tp : / /ees .e lsev ie r .com/ jas rep
Central Mediterranean Phoenician pottery imports in the NortheasternIberian Peninsula
Eva Miguel Gascón a,⁎, Jaume Buxeda i Garrigós a, Peter M. Day b
a Cultura Material i Arqueometria UB (ARQUB, GRACPE), Dept. de Prehistòria, Història Antiga i Arqueologia, Universitat de Barcelona, Montalegre 6, 08001 Barcelona, Catalonia, Spainb Department of Archaeology, University of Sheffield, Northgate House, West Street, Sheffield S1 4ET, United Kingdom
⁎ Corresponding author.E-mail addresses: [email protected] (E. Miguel
Article history:Received 19 December 2014Received in revised form 8 June 2015Accepted 9 June 2015Available online 18 June 2015
Keywords:Iron AgePhoenician commerceX-ray fluorescenceX-ray diffractionThin-section petrographyScanning electron microscopy
Over recent years, there has been a growing interest in the analytical investigation of Phoenician pottery recov-ered from sites in Catalonia (NE Iberian Peninsula). Studies which integrate mineralogical, chemical and micro-structural analysis have been carried out at seven sites in the Ilercavonia and Cossetania areas, analysing a total of123 ceramic samples. The characterization of these samples has confirmed the presence of Phoenician CentralMediterranean pottery, all in the form of tableware.Themain objectives of this paper are to determine the provenance of these products, to study theirmineralogicalcharacteristics and to understand the consumption of this Phoenician Central Mediterranean pottery in thecontext of the sites of Ilercavonia and Cossetania.All individuals have been analysed by means of X-ray fluorescence (XRF) and X-ray diffraction (XRD), withselected samples analysed by means of thin-section petrography and scanning electron microscopy (SEM). Theresults of this study demonstrate the presence of Sicilian, Sardinian and Tunisian products, allowing us to seepreferences of vessel types according to source.
Since 2002, analyses have been performed at the Universitat deBarcelona on the first wheel-thrown pottery found in indigenouscontexts of the VIII century–575 BC in the regions of Ilercavonia andCossetania (Catalonia). Traditionally, this pottery has been thought tohave been manufactured by potters located in a variety of WesternPhoenician colonies.
Most of this pottery comprises amphorae whose provenance hasbeen associated with the Circle of the Strait of Gibraltar, where the an-cient Phoenician colonies (Aubet, 2009) of the Iberian Peninsula and At-lantic Sea were located (Fig. 1). In the last years, a complex Phoeniciancabotage system has been suggested (Rafel, 2013), starting from theseSouthern Andalusian sites, reaching along the Iberian Peninsula coastto the indigenous communities situated in Catalonia. This contactseems to have been commercial in nature, since there are no Phoeniciancolonies in the Ilercavonia and Cossetania regions. In fact, it is in theprovince of Málaga in Andalusia where intense archaeological workhas revealed an extensive list of Phoenician sites, settlements and pro-duction centres (Toscanos, Cerro del Villar, La Pancha, Los Algarrobeños,Chorreras, Morro de Mezquitilla) and most studies of Phoenician pot-tery found in Catalonia point to this area as its source (Garcia and
Gracia, 2011). However, amongst the Phoenician pottery found in theCossetania and Ilercavonia regions of Catalonia, a small group, mainlytableware, is not related to a source area of the Circle of the Strait ofGibraltar.
Macroscopic study has proved of limited value in ascribing prove-nance to these vessels. As a result one of the main objectives of the an-alytical research reported here is to define the different CentralMediterranean Phoenician products detected at three sites in NortheastIberia (Fig. 2): Sant Jaume-Masd'en Serrà and La Ferradura (Ilercavonia)and Turó de la Font de la Canya (Cossetania). In this paper we presentsome of the results of Miguel Gascón's unpublished Doctoral Thesis(Miguel Gascón, 2014).
The site of Sant Jaume-Mas d'en Serrà (Garcia and Gracia, 2011) hasdifferent types of pottery related to Central Mediterranean production.There are three narrow-necked cylindrical jars (MOS026, MOS040 andMOS060) and a carinated red slipped bowl (MOS037). The settlementfeatures a defensive system unique in the whole of the NortheasternIberian Peninsula during the Early Iron Age (Garcia, 2009). It seemsthat in Catalonia, Sant Jaume was one of the centres with the strongesttrade relations with the Phoenician world, thus up to 30% of the wheel-made pottery excavated is related to Phoenician imports (Garcia et al.,2015).
The other Ilercavonian site included in this study is La Ferradura(Maluquer, 1983), where only one indeterminate pot was related to aCentral Mediterranean provenance (FER005). The settlement hosts acomplex of eleven rooms, some clearly related to metallurgical activity.
Fig. 1.Western Phoenician colonies and Phoenician production centres located at the Circle of the Strait of Gibraltar.
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Most Iron Age sites of Ilercavonia are related to metallurgy, whichseems to be closely connected with Phoenician commerce.
In the case of Turó de la Font de la Canya (Asensio et al., 2005), fournarrow-necked cylindrical jars (TFC025, TFC036, TFC040, and TFC041)
Fig. 2. Location of the sites sampled where Central
and one oil bottle (TFC072), were identified as Central Mediterraneanproducts. This site is a campo de silos, a large area full of silos devotedto the storage of the product of a system of intense cereal exploitation.This type of settlement is predominant in the Cossetania region.
Mediterranean Phoenician products are found.
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2. Methods
2.1. X-ray Fluorescence (XRF)
To characterize the chemical composition of these samples (Table 1),XRF was carried out in the Centres Científics i Tecnològics of theUniversitat de Barcelona. Due to the long duration of the researchproject, two different XRF instruments were used. More detailed infor-mation about the analytical routine has been published elsewhere(Miguel Gascón and Buxeda i Garrigós, 2013).
First, in the case of samples MOS026, MOS037 and MOS040, majorand minor elements (MgO, Al2O3, SiO2, P2O5, K2O, CaO, TiO2, MnO, andFe2O3 — as total Fe) were determined by preparing duplicates of glassbeads. Trace elements (V, Cr, Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Mo,Sn, Ba, Ce, W, Pb, and Th), as well as Na2O, were determined by pow-dered pills. The quantification of the concentrations was performedusing a (WDXRF) Phillips PW2400 spectrometer with an Rh excitationsource.
Samples MOS060, FER005, TFC025, TFC036, TFC040, TFC041 andTFC072 were analysed with a different XRF machine. In this case,major and minor elements (including Na2O) were determined byduplicates of glass beads. Trace elements were also determined bypowdered pills. However, this time determination of concentrationswas performed using an AxiosmAX-Advanced PANalytical spectrometerwith an Rh excitation source.
All differences between the two XRF machines were taken intoaccount in order to be able to compare the data obtained.
2.2. X-ray Diffraction (XRD)
The mineralogical composition was studied by means of XRD at theCentres Científics i Tecnològics of the Universitat de Barcelona.
Measurements for samples MOS026, MOS037 and MOS040 weremade using a Siemens D-500 diffractometer working with the Cu-Kαradiation (λ = 1.5406 Å) at 1.2 kW (45 kV–30 mA). Measurementswhere taken from (4 to 70) °2θ, at 1°2θ min−1 (step size = 0.05°2θ;time = 3 s).
In the case of samples MOS060, FER005, TFC025, TFC036, TFC040,TFC041 and TFC072 measurements were made using a Bragg–BrentanoPANalytical X'Pert PRO MPD Alpha diffractometer equipped with an
Table 1Normalized concentrations of the chemical compositions of the analysed samples.
X'Celerator detector, working with the Cu-Kα radiation (λ =1.5406 Å) at 1.8 kW (45 kV–40 mA). Measurements where taken from(4 to 100) °2θ, with a step size of 0.026°2θ and an acquisition time of50 s per step.
2.3. Thin-section Petrography
Samples MOS037, MOS040, FER005, TFC025, TFC036, and TFC041were also analysed in terms of thin-section petrography at theUniversi-ty of Sheffield. All specimens were cut transversely to the direction ofthe wheel-thrown marks using an Evans saw. Thin-sections wereexamined at a range ofmagnifications from×25 to ×100 under a petro-logical microscope to study their mineralogy, petrography and texture.Petrographic groups were described following Whitbread's system(Whitbread, 1989, 1995).
2.4. Scanning Electron Microscopy (SEM)
Finally, some specimens (TFC041, TFC036 andMOS037)were select-ed for analysis by SEM attached to an energy-dispersive X-ray analyser(EDX) in order to characterize the microstructure and the sinteringstage of the ceramic matrix and to identify aplastic inclusions. Thus,fresh fractures of the observed samples were coated with a carbonlayer in a high vacuum atmosphere. An acceleration voltage of 20 kV,beam current of 1 nA, and 100 s per microanalysis were used.
These analyses were carried out at the Centres Científics iTecnològics of the Universitat de Barcelona, using a JEOL JSM-6510and Quanta 200 microscope.
3. Results
The elemental concentrations determined by means of XRF are aspecial case of the projective d + 1-dimensional space, the simplex Sd.Projective points are represented by a d + 1-dimensional vector of co-ordinates adding up to a constant k (k ∈ R+),
x ¼ x1;…; xdþ1½ � xi ≥ 0j i ¼ 1;…; dþ 1ð Þ; x1 þ…þ xdþ1 ¼ k;
(in the present case, k = 100), a subset in the positive orthant Rd + 1,following a multiplicative model with logarithmic interval metrics
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(Barceló-Vidal et al., 2001; Aitchison, 2005; Buxeda i Garrigós, 2008).Therefore, for the statistical data treatment, raw concentrations havebeen ALR (additive log-ratio) transformed, according to
x ∈ Sd→y ¼ logxd
xdþ1
� �∈ Rd;
being Sd the d-dimensional simplex, x−D= [x1,…,xd], and D= d+1, orCLR (centred log-ratio) transformed, according to
x ∈ Sd→z ¼ logx
g xð Þ� �
∈ Rdþ1;
being Sd the d-dimensional simplex, and g(x) the geometric mean of allD (D = d + 1) components of x (Aitchison, 1986; Buxeda i Garrigós,1999). Moreover, several elements were discarded: Mo and Sn due tolow analytical precision, and Co andW because of the possible contam-inations from the tungsten carbide cell of themill. Thwas also not takeninto account, on account of possible interferences due to the high Srconcentrations, that could not be corrected in the case of those analysesdone with the (WDXRF) Phillips PW2400 spectrometer.
A cluster analysis was performed with R software (R Core Team,2013) using the square Euclidian distance and the centroid agglomera-tive algorithm on the subcomposition Na2O, MgO, Al2O3, SiO2, K2O, CaO,TiO2, MnO, and Fe2O3, with CLR transformation of the 218 Phoeniciansamples of theARQUBdatabase (Fig. 3). Onlymajor andminor elementswere considered in this statistical treatment since the abovementioneddataset included 178 specimens analysed by other research teams.These individuals belong to Phoenician pottery or to chronologically re-lated ceramics, but only major and minor element concentrations weredetermined. Moreover, since the analytical routine was also differentfrom the present project and, in most cases, there are no inter-laboratory calibration studies, this comparison should be consideredsemi-quantitative. The analytical case studies of these 178 specimensare: a study conducted at the Università di Palermo on the Phoenicianproductions of Mozia and Solunto in Sicily (Alaimo et al., 1998, 2002);three studies conducted at the Istituto di Ricerche Tecnologiche per laCeramica — CNR (Faenza) on the Phoenician tableware of Carthage
Fig. 3. Dendrogram illustrating cluster analysis of the 218 Phoenician individuals ofARQUB's database, along with the 178 published samples.
(Amadori and Fabbri, 1998a), Toscanos (Amadori and Fabbri, 1998b),Sardinia (Tharros, Santo Antioco and Monte Sirai), and Ischia(Amadori and Fabbri, 1998c); the grey products from the Iberian siteof Ullastret (Pradell et al., 1995); the amphorae of the Palaià Polis ofEmpúries (Vendrell-Saz, 2005); and the Phoenician kilns of Cerro delVillar (Cardell, 1999). In the case of Carthage, Sicily and Sardinia, controlgroups were formed by samples classified as local products on groundsof their typology, and their chemical and mineralogical analysis bymeans of XRF and thin-section petrography.
The statistical data treatment is summarized in the dendrogramresulting from the cluster analysis in Fig. 3. It shows a complex structurewhere we observe groups related to Central Mediterranean sources,according to the comparative data bank considered. Thus, group CERcontains a possible Sardinian sample (MOS037), while a possibleSicilian provenance can be suggested for sample FER005, which is in-cluded in group SIC. Also of interest is a possible Tunisian (Carthaginian)provenance for samples TFC025, TFC036, TFC040, TFC041, TFC072,MOS026, MOS040 and MOS060 in the complex structure CAR that canbe divided into four different groups: CARa, CARb, CARc and CARd.
There follows an assessment of the chemical and mineralogical dataobtained through the XRF, XRD, SEM and petrographic analysis for eachof these groups.
3.1. Carthaginian Products: GR CARa, CARb, CARc and CARd
The compositional variationmatrix enabled the quantification of thetotal variation (vt) present in the data matrix and the investigation ofthe source of this variability. In the case where all samples belongingto the CARa, CARb, CARc and CARd subgroups were considered as onegroup (CAR), vt has a high value (vt = 1.8). This suggests that thesedata have a polygenic character, which means that not all individualsexhibited similar compositions; so, following the provenance postulate,it would be expected that they represent different units of production(Buxeda i Garrigós and Kilikoglou, 2003). This chemical variability islinked to Ba, MnO, CaO, Na2O, Th, Cu and Cr. The element that imposesthe lowest relative variation is Al2O3 when used as divisor in ALRtransformation and will, therefore, be used in the statistical datatreatment (Buxeda i Garrigós, 1999). Because of the extreme variabilityintroduced by Na2O and Ba these elements were excluded from thestatistical data treatment. Also Pb, Cu and P2O5 were not used becausethey are known to be sensitive to post-depositional perturbations.
A cluster analysis was performed, using the Euclidian distance andthe centroid agglomerative algorithm on the subcomposition MgO,SiO2, K2O, CaO, TiO2, V, Cr, MnO, Fe2O3, Ni, Zn, Ga, Rb, Sr, Y, Zr, Nb, andCe, ALR transformed using Al2O3 as divisor.
Fig. 4 shows the dendrogram resultant from this statistical treat-ment. The first group that appears, CARa, includes individuals MOS040and MOS060 that present the lowest CaO concentrations amongst theTunisian groups (9.60%, Table 2). Next to it, another group, CARb, withsamples TFC025, TFC040 and TFC041 presents the highest concentra-tions in Rb (114 ppm, Table 2). Regarding CARc, a single individual is in-cluded (TFC072), which is the most calcareous specimen of theCarthaginian products analysed (26.1% in normalized data, Tables 1and 2). Finally, CARd, presents the highest concentrations of Zn for sam-ples TFC036 and MOS026 (94 ppm, Table 2).
Petrographic analysis was performed on individuals MOS040(CARa); TFC025, TFC041 (CARb); and TFC036 (CARd). It was possibleto identify different petrographic groups:
Group 1 This group is represented by sample TFC036 (Fig. 5), charac-terized by the presence of rounded quartz and calcite inclu-sions. There are very rare to rare voids forming an estimatedb1% of the volume. Open-spaced common mesovughs, raremesochannels and elongate voids, have a strong alignmentto the vessel wall. Mostly equant aplastic inclusions exhibita poor alignment parallel to the vessel wall.
Fig. 4. Dendrogram of the eight Phoenician individuals of possible Carthaginian prove-nance after cluster analysis.
Fig. 5. Group 1: Photomicrograph, showing rounded quartz and calcite inclusions. TFC036(fabric CARd-II) in XP (×25).
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It presents a fine, dense calcareous matrix homogeneousthroughout the section. The colour is brown to greyish in PPLand dark brown in XP (×25). The micromass is optically inac-tive. The inclusions appear to have a bimodal grain-size
Table 2Mean (m), standard deviation (sd) and normalized concentrations of the chemical compositio
distribution; the coarse fraction is set in a finer-grained ground-mass. It is generally sub-rounded to well-rounded and wellsorted. Micro-fauna composed by foraminifera of globigerinidaspecies are present in the coarse fraction. Calcite crystals havereplaced the multi-chambered walls and, in very rare cases,they also contain iron oxide (size b 0.08 mm). This type of mi-crofossil is also common in the fine fraction (size b 0.04 mm,mode = 0.025 mm). The abundance of these microfossils andsandstone indicates a sedimentary environment.
Group 2 The dominant inclusion of this fabric consists of crushed cal-cite. It is represented by sample TFC025 (Fig. 6). Its micro-structure presents very rare voids, with few mesovughsand very rare mesochannels. It is possible to see elongatevoids which are open-spaced distributed and display strongalignment to the margins of section with. Elongate andequant aplastic inclusions exhibit a moderate alignment tothe vessel walls.
Fig. 6. Group 2: Photomicrograph illustrating crushed calcite inclusions. TFC025 (fabricCARb-I) in XP (×25).
Fig. 7. Group 3: Photomicrographs showing allotriomorphic quartz and mica matrix.TFC041 (fabric CARb-I) in XP (upper) and MOS040 (fabric CARa-I) in XP (lower) (×25).
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It features a fine calcareous matrix predominantly homoge-neous throughout the section. It is brown/orange in PPL andbrown/red in XP (×25) and optically very active. Crushedcalcite is the dominant inclusion in coarse fraction, angular,euhedral and equant and well sorted (size b 0.32 mm,mode = 0.15 mm).Textural concentration features (Tcfs) are bright red in PPLand dark red in XP (×25) with clear to merging boundariesand very high optical density. They are generally equant,and rounded and have high sphericity, discordant withthe micromass. They commonly display fine-grainedmonocrystalline quartz inclusions, with varying amountsof ferruginous matter, sometimes almost opaque. They areprobably clay pellets (size 0.036 mm to 0.016 mm).The angular and even regular shape of calcite inclusionspresent in this sample suggests that this mineral wascrushed and added deliberately to the clay as temper.
Group 3 This is defined by allotriomorphic quartz and mica aspredominant inclusions in the matrix (samples MOS040and TFC041, Fig. 7). The microstructure shows rare tofew voids, forming an estimated 1–3% of the volume.There are common meso- and microvughs and raremesochannels. Elongate voids have a very strong align-ment to the margins of sections and are single to double-spaced. These display partial infilling with secondarycalcite. The equant, aplastic inclusions mostly exhibit apoor alignment to the vessel walls.The predominantly fine calcareous and homogeneous ma-trix is brown in PPL and dark orange/brown in XP (×25).The micromass is optically active, evident in MOS040,due to a low firing temperature.Quartz (size b 0.032 mm, mode = 0.018 mm) and musco-vite mica (size b 0.024 mm, mode = 0.015 mm) are fre-quent in the fine fraction. Calcite is common and thereare few iron oxides and opaques. Rare foraminifera micro-fossils are present in TFC041.There are two different types of Tcf in sample TFC041. Thefirst is dark orange in PL and brown in XP (×25), with clearboundaries and is optically dense. This type is generallysub-angular, discordant with the micromass and containsnon-plastic inclusions of fine, monocrystalline quartz andcalcite crystals (size b 0.16 mm, possible clay pellets). An-other Tcf is of dark red colour in PPL and XP (×25) almostopaque, with clear, sharp boundaries. In some case thereis a surrounding void. Optically it is extremely dense and
sub-angular, discordant with the micromass, with non-plastic inclusion, such as fine-grained monocrystallinequartz, distinguishable (size = 0.3 mm, possible grog).Microfossils are more abundant and larger in MOS040, inboth the coarse and fine fractions. It is also possible to dis-tinguish foraminifera and crushedmolluscs (size b 0.1 mm,mode = 0.05 mm). The rounded to well-rounded mono-crystalline quartz fragments present in the matrix are a di-agnostic feature to relate these samples with a desertenvironment. It may be suggested that TFC041 is a finerversion of TFC025.XRD results allow the identification of different fabrics(Buxeda i Garrigós et al., 1995) within each chemicalgroup of the Carthaginian products. In the case of groupCARa there is just one fabric, CARa-I, represented by sam-ples MOS040 and MOS060. It is possible to estimate a lowequivalent firing temperature (EFT) below (800/850) °C,since no firing phases were observed (Fig. 8, top).Again, only one fabric was defined for group CARb, com-prising samples TFC025, TFC040 and TFC041 (CARb-I). ItsEFT can be estimated below (800/850) °C.CARc contains only one sample, TFC072, (CARc-I). Thediffractogram of this oil bottle (Fig. 8, centre) presentsquartz, gehlenite, calcite, plagioclase and analcime, whichis a sodic zeolite that appears as a perturbation in highfired calcareous ceramics (Buxeda i Garrigós, 1999). ItsEFT can be estimated around (1000/1050) °C.
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Two fabrics can be distinguished for CARd. SampleMOS026 represents fabric CARD-I with a low EFT, below(800/850) °C. Fabric CARd-II is represented by sampleTFC036 (Fig. 8, bottom) with an EFT estimated c. (950/1000–1050) °C. This EFT, similarly to the CARc-I fabric, isindicated by the total decomposition of illite–muscoviteand the crystallization of plagioclase, pyroxene andgehlenite. Therefore, the presence of calcite must be asso-ciated with a secondary origin, as observed in petrographicanalysis (Cau Ontiveros et al., 2002).The study of these products was completed by SEM analysis.Fabric CARb-I was studied through sample TFC041 and it waspossible to confirm its low firing (Fig. 9, top), through its non-vitrificated (NV) matrix (Kilikoglou, 1994). The EFT couldthus be below 750 °C. Fabrics CARa-I, CARc-I and CARd-Iwere not analysed. In fabric CARd-II a stage close to totalvitrification (Vc+–TV) was observed (Fig. 8) and its EFTcan be estimated at around (1050–1080) °C.
3.2. Sardinian Production: GR CER
Sample MOS037 can be related to a Sardinian provenance. This redslip carinated bowl is grouped together with the reference groups of thePhoenician site of Sulcis (Acquaro, 1998; Amadori and Fabbri, 1998c). Itpresents high concentrations in Na2O, K2O, Rb, Y, and Ce (1.92%, 4.41%,182 ppm, 46 ppm, and 121 ppm in normalized data, respectively, Table 1).
Petrographic analysis characterized MOS037 as a different group,where Tcfs are the principal inclusion (Fig. 10).
Group 4 There are rare to very few voids in this sample: commonmesovughs, single to open spaced, elongate andwith a strongalignment to the section margins. Elongate and equantaplastic inclusions exhibit moderate alignment parallel tothe vessel walls.The sample has a fine calcareous, largely homogeneous ma-trix, which is light brown to greyish-brown in PPL andorange-reddish to brown in XP (×25). Frequent Tcfs occur inboth the coarse andfine fractions. They are dark red to opaquein PPL and brown-reddish to opaque in XP (×25), with sharpto clear boundaries and very high optical density. They areusually angular to sub-angular and discordant with themicromass. Some have monocrystalline quartz and calcite in-clusions similar to those in the matrix. Their angularity mightsuggest that they are grog fragments, although they may beclay pellets (size b 0.24mm,mode=0.112mmin coarse frac-tion and size b 0.08 mm, mode = 0.032 mm in fine fraction).The CaO concentration of MOS037 shows us that it is non-calcareous (1.64% in normalized data, Tables 1 and 2). InXRD analysis (CER-I), no firing phases are observed (Fig. 11)and the estimated EFT is below (800/850) °C.SEM confirms the low firing suggested by the XRD spectra. InFig. 12, themicrostructure of thematrix displays initial to justless than continuous vitrification (IV–Vc−). Thus, the EFT is inthe range (750–850) °C.
3.3. Sicilian Production: GR SIC
Sample FER005, from La Ferradura, is related by chemistry to thePhoenician production centre of Solunto (Sicily), and thus was labelled
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group SIC (Acquaro, 1998; Alaimo et al., 1998). It is illustrated in thinsection in Fig. 13.
Group 5 Sandstone inclusions and serpentinite are the most com-mon features of this sample. There are very rare voids,
Fig. 10. Group 4: Photomicrograph illustrating textural concentration features/grogtemper. MOS037 (fabric CER-I) in XP (×25).
comprising common mesovughs, open-spaced, elongatewith a strong alignment to the margins of sections. Somehave traces of secondary calcite infilling. Elongate andequant aplastic inclusions exhibit a poor alignment to thevessel walls.It presents an optically active, fine calcareous matrix homo-geneous through the section, greyish to brown/orange inPPL and dark brown to orangish-red in XP (×25).There is dominant sub-rounded to rounded monocrystal-line quartz in the coarse fraction (size b 0.176 mm), sub-rounded to rounded calcite (size b 0.16 mm), with micro-fossils composed of foraminifera and mollusc fragments(size b 0.07 mm). More rarely it is possible to identify mica-schist (size b 0.108 mm).Tcfs are dark in colour in PPL and red in XP sub-angular to sub-rounded with clear boundaries (size b 0.25 mm).XRD analysis of this calcareous fabric (12% of CaO in normal-ized data, Tables 1 and 2) (designated fabric SIC-I) suggests alow EFT, c. (800/850) °C. It contains illite–muscovite, quartz,calcite, hematite, potassium feldspars and plagioclase(Fig. 14). No SEM analysis was performed because of thelack of specimen.
Fig. 12. SEM photomicrograph of MOS037 (fabric CER-I).
Fig. 13. Group 5: Photomicrograph showing sandstone inclusions and serpentinite.FER005 (fabric SIC-I) in XP (×25).
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4. Discussion
The Carthaginian imported vessels identified in this study are calcar-eous (CARa) to highly calcareous (CARb, CARc and CARd). They containverywell rounded quartz, alongwith possible indications of claymixingand sand tempering. These technological features have been observedin the Phoenician production of Tyre (Miguel Gascón, 2014). Moreover,in the case of TFC025 (CARb), crushed calcite is used as temper, a tech-nique also observed at the Phoenicianmetropolis. XRD has also revealedthat most of these fabrics exhibit low EFT (below 800 °C), similar to thatof the pottery produced at Tyre (Miguel Gascón and Buxeda i Garrigós,2013). It should be emphasized that the agreement between datafrom XRF and thin section petrography is not complete and that itremains to be shown whether these represent only Carthaginianproducts, or those of other Tunisian production centres.
The Sardinian imports, group CER, seems to be related to a differenttradition especially since grog may be used as temper. Moreover, it is
also a non-calcareous fabric and this lies in contrast with the technologyof Carthaginian or Tyrian production.
Finally, group SIC is calcareous, low-fired (EFT below (750/800) °C),with inclusions compatible with the geology of the Solunto area inSicily. It presents more similarities with Tyrian ceramics than thegroup CER.
It is of interest that the Ilercavonia and Cossetania sites do not haveamphorae from these Central Mediterranean sites, only tableware.Amongst the 220 samples examined in this study, it was clear thatmost of the amphorae analysed have an Andalusian origin, especiallyfrom the areas of Málaga and Granada (Miguel Gascón, 2014). Alsowhile the archaic Phoenician colonies in Southern Iberia produced redslip tableware and jars, none arrived in the study area. Indeed, whilegenerally rare, the Phoenician tableware at these Northern regions isclearly from the Central Mediterranean production centres. This mayindicate an important consumption preference. However, furtherresearch is needed in other sites of the early Iron Age in the Ilercavoniaand Cossetania regions to confirm that pattern.
5. Conclusions
The appearance of Phoenician imports in the early Iron Age contextsof the Cossetania and Ilercavonia regions is notable not only for the firstevidence of wheel-made pottery, but also in terms of the novel con-sumption of the products transported in these jars. This latter changein consumption and contact may have had deep social implications.The rarity of tableware in the sites studied is notable, but, when it ispresent, the choice of Central Mediterranean tableware and the totalabsence of Andalusian red slip demand explanation and clearly havemeaning in socio-economic terms.
Moving to the production centres of these imported CentralMediterranean vessels, it seems that there is a clearer link betweenthe Carthaginian products and those of Tyre, than those produced inSardinia and Sicily. However, clearly such judgements on the natureand cultural context of production at these centres require largersample numbers and the detailed study of production technology inthe source assemblages in Tunisia, Sicily and Sardinia.
Acknowledgements
This study was made possible by David Garcia i Rubert, through hisgenerous permission to study the materials of Sant Jaume-Mas d'enSerrà and La Ferradura and by Rafel Jornet Niella, David Asensio Vilaró,Jordi Morer de Llorens and Daniel López Reyes who allowed us toinclude the samples from Turó de la Font de la Canya in this study.
The XRF, XRD and SEM analyses presented were carried out in theCentres Científics i Tecnològics of the Universitat de Barcelona. The pet-rographic analyses were carried out at the Department of Archaeology,University of Sheffield.
EvaMiguel Gascón is indebted to the JAE-Predoc programme fundedby the CSIC.
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