Introduction and objectives

This investigation is part of the ongoing research project of one of us (MVL)Footnote 1, which aims at shedding light on the ceramic production in the late medieval and early modern periods in the areas of the ancient Kingdoms of Córdoba and Granada. The Kingdom of Córdoba, like those of Jaén and Seville, was conquered during the first half of the thirteenth century (Córdoba in 1236, Jaén in 1246 and Seville in 1248). On the contrary, the Nasrid kingdom of Granada lasted until the end of the fifteenth century (Granada War 1482-1492). The researchers’ attraction for the splendour and glory of the Islamic world has put aside the study of ceramic production and distribution after the Christian conquest. In contrast, Islamic ceramic production has been profusely studied in the last decades, both from an archaeological and archaeometric point of view. Thus, the project’s main objectives are to define the products of the Christian Cordoban and Granadian workshops since the fifteenth century and their diffusion through the archaeometric characterisation and the definition of their reference groups (RG). In this paper, we focus on studying the case of workshops and consumption centres of the city of Córdoba after the Christian conquest, from the late medieval to the early modern periods. For this reason, samples from different workshops from Córdoba (fifteenth–seventeenth centuries) (37° 53′ 00′′ N, 4° 46′ 00′′ W), Priego de Córdoba (sixteenth–seventeenth centuries) (37° 26′ 18′′ N, 4° 11′ 53′′ W), Granada (sixteenth–eighteenth centuries) (37° 10′ 41′′ N, 3° 36′ 03′′ W) and Cártama (fifteenth–sixteenth centuries) (36° 42′ 41′′ N, 4° 37′ 50′′ W), and also from different consumption centres in Córdoba (seventeenth–eighteenth centuries), Granada (fifteenth–eighteenth centuries), Coín (fourteenth–sixteenth centuries) (36° 39′ 32′′ N, 4° 45′ 25′′ W) and Castillo de Montejícar (fifteenth–sixteenth centuries) (37° 34′ 19′′ N, 3° 30′ 16′′ W) are considered in this project (Fig. 1)Footnote 2.

Fig. 1
figure 1

Location of the sites cited in the present paper

The Kingdom of Córdoba was a territorial jurisdiction of the Crown of Castile after conquering the town in 1236. Córdoba was directly affected by the two important events that marked the start of the early modern period: the Christian conquest of Granada and the colonisation of the Americas (starting in 1492). On the one hand, the conquest of Granada entailed the disappearance of the borders between the Muslim Kingdom of Granada and the Christian Kingdom of Córdoba. On the other hand, the colonisation of the Americas significantly affected the demography of the city of Córdoba, which received people from other regions of the Iberian Peninsula and Europe attracted by the new commercial opportunities. Moreover, people from Córdoba went to the American colonies and contributed to the conquest of new territories and the foundation of cities and villages. Although the primary commercial relationships between the Castilian Crown and the American colonies took place on the Atlantic Coast of Andalusia, the city of Córdoba benefited from the creation of new economic structures and networks (Escobar 2008, p. 19). In this sense, the ceramic production in the Kingdom of Córdoba in the early modern period could have been influenced by the so-called ‘Carrera de Indias’ (the monopoly of the permanent trade route and navigation between the Crown of Castille and the American colonies), consolidating local and regional production centres and, possibly, enabling to export transport jars and other ceramics (Hughes 2014; Kingsley et al. 2014).

Since medieval times, the city of Córdoba has been structured in two main areas, where residential and commercial activities coexisted: Villa (called Medina in the Islamic period) and Axerquía (Escobar 1989, 2008). The Barrio de las Ollerías (potter’s quarter) was located north outside the Axerquía walls. Urban rescue excavations and historical documentation reveal that the Barrio de las Ollerías was the main ceramic production area from the early medieval until the end of the early modern periods, thanks to its proximity to important natural clay sources, water and combustible material. The structures and materials linked to these potters’ activity include kilns (but only for the Islamic period), dumps, wasters and other objects like kiln rods, saggars and trivets. Ceramics related to these workshops have been studied only for the Islamic period (Aparicio 2016; Molina and Salinas 2010, 2013), and no systematic research concerning the Christian period has been carried out by historians based on written sources or by archaeologists. The only relevant exception is the study of archive sources from the fourteenth to fifteenth centuries that provide information about production techniques and typologies. Cooking pots, casseroles and ‘tinajas’ (big jars for liquids, grains or other solid elements) produced in the Barrio de las Ollerías are the most common types mentioned in the written records. Concerning cooking ware, historical documentation remarks on the low quality of the products made in Córdoba, which frequently broke down when heating (Córdoba de la Llave 1988–1989, 1990, 1997).

This paper considers tin-lead glazed vessels, coarse ware, cooking ware, storage and transport jars and trivets recovered from three different archaeological sites of the Barrio de las Ollerías, plus the consumption context of Casa Carbonell, in the Villa area (Fig. 2). The latter is probably related to a convent and offers a well-defined stratigraphic sequence and a significant amount of tin-lead glazed pottery. It is important to highlight that this kind of ceramics is not commonly found in the excavations of modern production centres of Córdoba, and the archives do not mention it, raising the problem of whether tin-lead glazed ceramics were locally produced. This study integrates the archaeological data (morphological and decorative characteristics of the pieces) and the archaeometric approach (chemical and mineralogical composition and technical aspects) to define the products of the workshops and their diffusion and identify products of non-local origin. Within this framework, the main objectives of the paper are to (i) identify meaningful ceramic reference groups (RG) (Buxeda and Madrid 2016) of the Cordoban workshops under study, (ii) to provide information on some technical aspects of the local products and (iii) to compare the analytical results with the morphological characteristics of the studied ceramics. Establishing a connection between typologies, decorations, chronologies and the archaeometric results will help improve the classification of ceramics found in consumption centres and the historical interpretations leading to a better understanding of the social and cultural context.

Fig. 2
figure 2

Map of Córdoba with the location of the sites under study. Based on the map “El Plano de los Franceses” (Baron of Karwinsky and Rillo 1811)

The new data obtained in this study have been compared with the ARQUB database, which includes many analytical results concerning different kinds of late medieval and early modern pottery from production and consumption centres in the Iberian Peninsula and the Atlantic American colonies. These analyses are included in the Tecnolonial project devoted to deepening the knowledge of the interaction, influence and cultural change during the colonisation process in the Americas during the sixteenth–seventeenth centuries through the archaeological and archaeometric study of ceramics. Incorporating more archaeological workshops such as those from Córdoba allows us to improve the knowledge of the complex network of pottery production and distribution over the entire Iberian Peninsula and the American colonies at that time.

The new results have contributed to six new reference groups, besides identifying allochthonous products from a known and unknown origin in the city of Córdoba.

Materials and methods

One hundred and twenty individuals recovered from several archaeological sites in Córdoba have been studied for this project. The criteria for the sampling was to have a representative amount for each archaeological site, including both production and consumption centres. So we considered studying 30 individuals for each of the four archaeological contexts described below. Different types of ceramics, such as tin-lead glazed vessels, coarse ware, cooking ware, storage and transport jars and kiln elements, have been considered (Tables 1 and 2). The sampling has been conditioned by the availability of each ceramic type in the different archaeological sites and the size of the sherds, which should be large enough to perform all the proposed analyses. The ceramics were recovered from three archaeological sites in the Barrio de las Ollerías (Fig. 2), where all the kiln structures date back to the Islamic period. However, in addition to ceramics, kiln furniture has also been identified in late medieval and early modern stratigraphic contexts for the Christian period. The first site is Avenida Ollerías 14 (37° 53′ 30.938′′ N, 4° 46′ 29.420′′ W)Footnote 3. Marfil excavated the site in 1990 to study the evolution of the Axerquía walls between the twelfth and the thirteenth centuries, unearthing a ceramic dump dated to the end of the fifteenth century (Marfil 1997). The second one, Ronda Marrubial (37° 53′ 32.316′′ N, 4° 46′ 1.884′′ W), was excavated by Vargas in 2009. In this context, several sixteenth-century ceramic materials related to kiln furniture and wasters were identified (Vargas 2010), revealing their connection with a production centre. Finally, the excavation of the third site, Hornos de San Cayetano (37° 53′ 31.157′′ N, 4° 46′ 31.447′′ W), was carried on by Aparicio in 2012. Several Islamic kilns were identified and studied, but also a fifteenth–sixteenth century ceramic dump was found. On this site, the ceramics span from the fourteenth–fifteenth to the seventeenth–eighteenth centuries (Aparicio 2012). Besides, the consumption context of Casa Carbonell (37° 52′ 55.632′′ N, 4° 46′ 47.856′′ W), in the Villa area, is also considered. This site was excavated by León and collaborators in 1991, and an interesting set of ceramics dated between the seventeenth and the eighteenth centuries could be recovered. It was interpreted as a dump related to a close Carmelite Convent (León et al. 1993).

Table 1 Studied individuals by site and ceramic class
Table 2 List of individuals studied in the present paper. CG: chemical group (post-analysis). For glazed pottery in = interior and out = exterior (if not stated, it is interior and exterior)

All the individuals have been chemically characterised through X-ray fluorescence (XRF) and mineralogically through X-ray diffraction (XRD). The chemical characterisation of the 120 individuals was performed using wavelength dispersive X-ray fluorescence (WD-XRF) analysis. Samples of around 15 g were taken from each individual. The superficial layers were mechanically removed, and the samples were milled in a tungsten carbide cell mill Spex Mixer mod. 8000. The chemical composition was determined from powder previously dried in an oven for 12 h at 105 °C. To determine the major and minor elements, two 30 mm glass bead replicates were made by mixing 0.3 g of dried sample with 5.7 g of lithium tetraborate (Li2B4O7) flux (1/20 dilution) and 5 mg of lithium iodide (LiI) as a release agent. This mixture was homogenised, deposited in a 95%Pt-5%Au crucible, and melted in a fully automatic bead preparation system PANalytical Perl'X-3 at a temperature of 1125 °C. To determine trace elements, pressed powder pellets were made using 6 g of specimen mixed with 2 ml of a binding agent solution of n-butyl methacrylate synthetic resin (Elvacite® 2044) in acetone at 20% by mass. This mixture was manually homogenised in an agate mortar to dryness and placed on a base of boric acid (H3BO3) in an aluminium vessel of 40 mm diameter that was subjected to a pressure of 200 kN for a period of 60 s using a Herzog press. The quantification of the concentrations was performed using an AxiosmAX-Advanced PANalytical spectrometer with an Rh excitation source calibrated by a suite of 56 international Geological Standards. Interferences were taken into consideration, and matrix effects were corrected using the PANanalytical Pro-Trace software for trace elements. The elements determined were Na2O, MgO, Al2O3, SiO2, P2O5, K2O, CaO, TiO2, V, Cr, MnO, Fe2O3 (as total Fe), Co, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Nb, Mo, Sn, Ba, Ce, W, Pb and Th. Major and minor elements are expressed as concentrations of oxides in mass fraction percentage (w %). Trace elements are expressed as concentrations of elements in μg/g. Loss on ignition (LOI) (expressed as w %) was determined by firing 0.3 g of the dried specimen at 950 °C for 3 h. Calcinations were carried out in a Heraeus muffle model M-110, using a heating rate of 3.4 °C/min and free cooling. Even so, some of the major and minor elements were discarded for statistical data treatment because of various problems: Co and W due to the possible contaminations from the tungsten carbide cell of the mill; Mo and Sn by low analytical precision and P2O5 and Cu given that several postdepositional processes easily alter them. Moreover, as has been observed in other studies that deal with glazed pottery (Buxeda et al. 2001; Iñáñez et al. 2005, 2007), many individuals present high concentrations of Pb, Sn and Cu due to the diffusion of the glazes in the ceramic matrix during the firing process. These high concentrations of Pb interfere with the signal from other elements and cannot be corrected. Thus, Ga, Rb, Y, Ce and Th are also discarded in the statistical treatment.

Mineralogical characterisation of the 120 individuals was performed by means of powder X-ray diffraction (PXRD). The previously prepared powder specimens were manually side-loaded and pressed with frosted glass in a cylindrical sample holder. Measurements were made using a Bragg-Brentano geometry diffractometer PANalytical X'Pert PRO MPD Alpha-1 (radius = 240 mm) using the Ni-filtered Cu Kα radiation (λ = 1.5418 Å) at a working power of 45 kV and 40 mA, equipped with an X'Celerator detector (active length = 2.122°). Measurements were taken from (5 to 80) °2θ with a 0.026° step size and an acquisition time of 50 s, spinning the sample at 1 Hz. The crystalline phases present in each analysed specimen were evaluated using the PANalytical X Pert HighScore Plus software package that includes the Powder Diffraction File™ (PDF®) of the International Centre for Diffraction Data (ICDD).

Results

Chemical analysis

The results of elemental concentrations of Córdoba samples analysed by XRF (Table 3) correspond with a special case of the projective d+1-dimensional space where the projective points are projected into the simplex 𝕊d. Points are represented by homogeneous coordinates that have a constant sum k (kR+),

$$\mathcal C\left(\mathbf w\right)=\mathbf x=\left[x_1,\dots,x_d,x_{d+1}\right]\mid x_i\geq0\;\left(\mathrm i=1,\dots,d,d+1\right),x_1+\cdots+x_d+x_{d+1}=k,$$
Table 3 Chemical concentrations by WD-XRF. Major and minor elements are expressed as oxides in w %; Trace elements in μg/g; LOI (loss on ignition) in w %

(in this current case, k = 100). The projective points’ vector space is the positive orthant. Both they and their projections in the simplex follow a multiplicative model. Hence, for the statistical data treatment, the raw concentrations have been alr (additive log-ratio) transformed according to

$$x\in\mathbb{S}^d\rightarrow y=\ln\left(\frac{x_d}{x_{d+1}}\right)\in R^d$$

being 𝕊d the d-dimensional simplex and xd = [x1,..., xd]. They have also been clr (centred log-ratio) transformed following the equation

$$\mathbf x\in\mathbb{S}^d\rightarrow z=\ln\left(\frac{\mathbf x}{\mathrm g\left(\mathbf x\right)}\right)\in H\subset R^{d+1}$$

being 𝕊d the d-dimensional simplex, g(x) the geometric mean of all d+1 components of x and ℍ ⊂ ℝd+1 a hyperplane vector subspace of ℝd+1 (Aitchison 1986; Buxeda 1999; Egozcue and Pawlowsky-Glahn 2011; Martín-Fernández et al. 2015; Buxeda 2018).

The statistical data treatment of the chemical data was performed using R (R Core Team 2021). The first analysis carried out was to calculate the variation matrix that completely determines the covariance structure of compositional data and provides the total variation (tv) of the analysed ceramic assemblage (Fig. 3, left) (Aitchison 1986; Buxeda and Kilikoglou 2003). The total variation for the overall data set equals 1.83, which means a high value indicating a polygenic group’s existence. The compositional evenness graph explores the variability associated with each retained component. When all components introduce equal variability, evenness is maximised, and the information entropy, or Shannon index, attains its maximum value (the logarithm with base two of the number of components) (Buxeda and Madrid, 2016). The more dominated the existing variability by a few or just one component, the more the information entropy drops significantly. The present graph reveals that the elements that introduce more variability are CaO and Sr (τ.j < 0.3), and, to a lesser extent, MnO, MgO and Na2O (0.3 < τ.j < 0.5). By contrast, Nb and V are the elements that introduce less variability, but their τ.j values are below 0.9. All these indicators show that even if the chemical variability is mainly linked to a few elements, the compositions vary significantly in all retained components (the information entropy has a value of 3.18 Sh, i.e. 77.73 % of the maximum attainable). In a more detailed exploratory analysis, it is easy to observe that individual CRB016 exhibits a significantly different composition, with very low MgO, CaO, MnO and Fe2O3 values and very high ones in Al2O3 and SiO2 (Table 3). As confirmed by its chemistry, this individual corresponds to porcelain and its extreme chemical differences will dominate the whole data treatment; therefore, this individual, a clear outlier, will be excluded in data treatment from now onwards. Once excluded, the compositional evenness graph (Fig. 3, right) reveals that the elements that now introduce more variability are, again, CaO and Sr (τ.j < 0.3) and, to a lesser extent and in a different order than previously, Na2O, MgO and MnO (0.3 < τ.j < 0.5). Again, Nb and V are the elements that introduce less variability, but their τ.j values are still below 0.9. The total variation and information entropy drop slightly to 1.73 and 3.13 Sh (i.e. 76.50 % of the maximum attainable), respectively, showing the individual CRB016 in increasing the differences in chemical composition reflected in the position changes of MgO, MnO and Al2O3. For the 119 individuals retained for analysis, the influence of CaO and Sr is essential to differentiate the calcareous and low-calcareous ceramics.

Fig. 3
figure 3

Left: Compositional evenness graph of the 120 studied individuals. Right: Compositional evenness graph of the 119 retained individuals, excluding CRB016. H2: information entropy (in shannons, Sh); H2 %: percentage of the maximum possible attainable; tv: total variation; τj: trace of the variance-covariance matrix following the alr transformation using element j as the divisor. Vertical dotted lines express different tv/τj values

To summarise the data treatment, we present the dendrogram (Fig. 4) from the cluster analysis performed on the 119 individuals from Córdoba using the square Euclidean distance and the centroid agglomerative algorithm on the subcomposition Na2O, MgO, Al2O3, SiO2, K2O, CaO, TiO2, V, Cr, MnO, Fe2O3, Ni, Zn, Sr, Zr, Nb and Ba, clr transformed. These results show a clear difference between low calcareous (CaO < 5–6%) ceramics placed in the left branch of the dendrogram and calcareous (5–6% < CaO < 25–35%) in the right one. The low calcareous individuals are classified into 3 groups, while the calcareous ones are classified into 10 groups, with 5 individuals remaining ungrouped. Three out of these five ungrouped individuals (pointed with black arrows in Fig. 4) are, in fact, of a Sevillian origin, as will be explained below.

Fig. 4
figure 4

Dendrogram from the cluster analysis on the subcomposition Na2O, MgO, Al2O3, SiO2, K2O, CaO, TiO2, V, Cr, MnO, Fe2O3, Ni, Zn, Sr, Zr, Nb and Ba, clr transformed, of the 119 individuals retained. Black arrows: ungrouped individuals of a Sevillian origin

To further investigate those groups, we compare these results with the ARQUB database, which includes a few thousand individuals from the main production centres of the Iberian Peninsula and different sites in the Americas and the Canary Islands. The statistical treatment gives information about the ceramic imports recovered in Córdoba, as well as the places where the Cordoban products were distributed. To summarise, in Fig. 5, we show the dendrogram from the cluster analysis on the previous subcomposition clr transformed, using the square Euclidean distance and the centroid agglomerative algorithm, of the 119 individuals from Córdoba compared to 334 relevant individuals from Priego de Córdoba (unpublished results), Granada (unpublished results), Villamartín (unpublished results) (36° 51′ 33′′ N, 5° 38′ 37′′ W), and Seville (Iñañez 2007; Buxeda et al. 2015; Fernández de Marcos 2019) (37° 23′ 00′′ N, 5° 59′ 00′′ W)Footnote 4. The comparison with the database shows no connections out of the area of Andalusia, showing local-regional networks between Córdoba and the territories around. Thus, we find ceramics from the cities of Granada and Seville in different archaeological sites in Córdoba (pointed with black arrows in Fig. 5), mainly in the consumption centre, but also appear in all production ones. These individuals correspond to calcareous pottery and are classified into the groups CGGRA, the one with an origin in Granada, and the CGSEV, whose origin is in Seville (Fig. 4). In this new dendrogram, it is clear that the previous ungrouped individual CRB013 has a Sevillian origin because this individual is classified in a new group of Sevillian ceramics. However, individuals CRB020 and CAY005 (pointed with green arrows in Fig. 5) are still ungrouped. As we will see in the next section, these individuals are affected by postdepositional processes that have altered their chemical concentrations in Na2O and K2O. Once these elements are not considered in the data treatment, these individuals are grouped with all Sevillian ceramics. Most of these Sevillian imports are tin-lead glazed sherds exhibiting different types of decoration: plain white (blanca lisa), manganese on white (blanco y manganeso), green on white (verde sobre blanco), Sevilla blue on white (azul sobre blanco), Yayal blue on white (azul lineal), Santo Domingo blue on white (azul figurativa), blue-green basin (verde y azul) and lusterware (loza dorada)Footnote 5. Furthermore, some examples of seventeenth-century plain white and Fajalauza ceramics from Granada have also been identified. Besides tin-lead glazed vessels, a few Sevillian individuals of transport jars and coarse ware are also present. In addition to these localised reference groups (RG), two paste compositional reference units (PCRU) of unknown origin could be defined (Bishop et al. 1982; Buxeda and Madrid 2016). The first group, labelled CGNC01, includes low calcareous individuals of honey-glazed dishes and bowls that have only been identified at Córdoba (Figs. 4 and 5). In contrast, the CGNC02 group, formed by three calcareous individuals of tin-lead glazed ceramics (Fig. 4), match a group of 5 individuals of unknown origin recovered at Granada (Fig. 5). The comparison with the database also shows that the remaining ungrouped individuals in Fig. 4 (OLL009 and CRB015, pointed with blue arrows in Fig. 5) are still outliers when comparing our results to the database, confirming them as loners. They correspond to fragments of a green-glazed bowl and an unglazed handle, respectively. The remaining 6 groups, labelled CGCRV, represent the product of Córdoba, and only two ceramics from group CGCRV05 have been identified out of this city, one in Villamartín—VLM040—and one in Priego de Córdoba—PRI011—(Fig. 5, pointed with red arrows).

Fig. 5
figure 5

Dendrogram from the cluster analysis on the Na2O, MgO, Al2O3, SiO2, K2O, CaO, TiO2, V, Cr, MnO, Fe2O3, Ni, Zn, Sr, Zr, Nb and Ba subcomposition clr transformed of the 119 individuals analysed in this study, compared with 334 relevant individuals of the ARQUB database. Red arrows: Cordoban products recovered in other archaeological sites. Black arrows: non-local ceramics recovered at Córdoba. Green arrows: Sevillian ceramics recovered at Córdoba but with altered compositions. Blue arrows: loners recovered at Córdoba

For a better understanding of the chemical differences in the studied set, we performed the singular value decomposition of the double-centred clr transformed data (Aitchison and Greenacre 2002; Greenacre 2010; van de Boogaart and Tolosana-Delgado 2013) on the 119 retained individuals, grouping together all ceramics from a Sevillian origin. The two first principal components' covariance and form biplots (Fig. 6) explain more than 80% of the variance (VE = 86.03%). The first principal component that explains most of the variance (VE = 76.51%) is mainly related to the ceramics’ low calcareous or calcareous nature. The components most involved in the group formation are CaO and Sr, together with MgO and Na2O (Fig. 6), attracted to the right-hand side, while K2O, MnO, Zr and Ba are attracted to the left-hand one. Moreover, the values of CaO and Sr are strongly correlated. The second principal component (VE = 9.52%) mainly shows Zr’s opposition, on the upper side, to MnO, on the lower one. Therefore, the Córdoban groups CGCRV01 and CGCRV02, the CGNC01 group of unknown origin, and the loner CRB016 (not used in this data treatment) correspond to low-calcareous pastes (Table 4) and are placed at the left-hand side of the biplots. All other groups and loners are considered calcareous. The CaO and Sr concentrations increase from left to right, reaching very high values in group CGNC02. Besides this component of calcareousness of the pastes, we can identify groups CGCRV01 and CGCRV03 at the upper side of the biplots because of their high concentrations of Zr and low ones of MnO. On the contrary, the group CGNC01 is characterised by very high concentrations of MnO, but K2O and Ba too. It is also important to highlight that groups CGCRV03, CGCRV04 and CGCRV05 show a continuous variation from low CaO and high Zr to high CaO and low Zr. Regarding the Sevillian group (CGSEV), it is easy to see that these ceramics exhibit high concentrations of MgO and Na2O. The highest MgO values are found in group CGGRA, exhibiting high MnO contents too. Finally, if we do not consider CaO and Sr concentrations in the statistic data treatment, groups CGCRV02 and CGCRV02c mingle. That suggests that the CGCRV02c group could have a similar origin as CGCRV02. Moreover, both groups exhibit high concentrations of MnO.

Fig. 6
figure 6

Covariance (left) and form (right) biplots of the singular value decomposition on the subcomposition Na2O, MgO, Al2O3, SiO2, K2O, CaO, TiO2, V, Cr, MnO, Fe2O3, Ni, Zn, Sr, Zr, Nb and Ba, double centred clr transformed. VE variance explained

Table 4 Mean (X̅) and standard deviation (s) of the defined groups and concentrations of loners (on normalized data). tv total variation. Major and minor elements are expressed in w %. Trace elements are expressed in μg/g

Mineralogical analysis

Chemical results show that the individuals analysed correspond to ceramics technically considered both low calcareous and calcareous. The individuals are distributed in different areas of the ternary phase diagrams CaO-Al2O3-SiO2 and (CaO+MgO+Fe2O3)-Al2O3-SiO2, also called the ceramic triangle, depending on their chemical composition (Fig. 7, left and right). As we can see, low calcareous groups and loner CRB016 are placed in the quartz–anorthite–mullite thermodynamic equilibrium triangle, while the calcareous ones are placed in the quartz–anorthite–wollastonite one. This difference in CaO content implies a marked technical difference between such products. Along these lines, the particular nature of the porcelain (CRB016) is made evident in Fig. 7, right where this individual appears isolated thanks to the extreme low contents of CaO, MgO and Fe2O3 in contrast with the very high Al2O3, corresponding to another very different technical solution. XRD results complete the information on the mineral phases, and they serve as the basis for estimating their equivalent firing temperature (EFT) when explained based on the chemical groups (Roberts 1963; Picon 1973; Tite et al. 1982; Heimann and Maggetti 2014; Gliozzo 2020).

Fig. 7
figure 7

Ternary phase diagrams of the (left) CaO-Al2O3-SiO2 and (right) (CaO +MgO+Fe2O3)-Al2O3-SiO2 systems with the situation of the individuals analysed. An anorthite (Ca[Al2Si2O8]), Gh gehlenite (Ca2Al(SiAl)2O7), Mul mullite (Al6[Si2O13]); Qz: quartz (SiO2), Wo wollastonite (CaSiO3) (abbreviations according to Whitney and Evans 2010)

The study of the XRD diffractograms enables identifying different fabrics, i.e. different categories of association of crystalline phases for each chemical group, that enables the establishment of mineralogical scales providing estimations for the EFT of the pottery shedding light on some aspects of the technical process (Buxeda and Madrid 2016: 36). Table 5 summarises the chemical groups and fabrics defined in this study, and Fig. 8 shows a selection of the 6 most relevant diffractograms analysed. In the following lines, we will discuss exclusively the fabrics identified in this study.

Table 5 Summary of the mineralogical fabrics defined by PXRD analysis for each chemical group
Fig. 8
figure 8

XRD patterns for the categories of association of crystalline phases as detected by XRD. a individual OLL28, group CGCRV03 (C), fabric F6; b individual CAY030, group CGCRV05 (C), fabric F4; c individual MRB019, group CGSEV (C), fabric F3; d individual CAY006, group CGSEV (C), fabric F9; e individual CRB009, group CGNC01 (LC), fabric F4; f individual CRB016, loner. Anl analcime, Cal calcite, Crs cristoballite, Gh gehlenite, Hem hematite, Ilt illite-muscovite, Afs alkali feldspar, Mul mullite, Pl plagioclase, Px pyroxene, Qz quartz, Sp spinel, Tc talc (abbreviations according to Whitney and Evans 2010)

The study of the diffractograms of the 6 individuals of the low calcareous group CGCRV01 enables defining three fabrics: F1 (OLL013, MRB020 and 028), F2 (MRB029 and CRB029), and F3 (MRB021). Although all these fabrics exhibit spinel, possibly as a firing phase, the difference in the presence or absence of illite-muscovite (the d(002) peak at 10 Å is always absent) enables estimating different EFT for F1 (< 950/1000 °C) and F2 (> 950/1000 °C). F3 also exhibits the presence of mullite, pointing to an even higher EFT (> 1000 °C).

The low calcareous CGCRV02 group contains 3 individuals classed in two different fabrics. Fabric F1 (MRB005) exhibits the presence of illite-muscovite (including the d(002) peak at 10 Å), but no firing phases are observed. The estimated EFT is below 900/950 °C. In contrast, fabric F2 (OLL002 and MRB010) exhibits the presence of spinel and illite-muscovite (without the d(002) peak at 10 Å). The estimated EFT is in the range of 950–1000 °C. The presence of calcite in all individuals must be due to a secondary phase (Buxeda and Cau 1995; Cau et al. 2002).

The CGCRV02c group behaves as a calcareous group and includes 4 individuals. The EFT estimated for F1 (OLL003) is 800–850 °C because of the absence of firing temperatures, possibly except for hematite. Fabric F2 includes one individual (MRB004) that exhibits clear firing phases (pyroxene, gehlenite and intense peaks of plagioclase) together with illite-muscovite. The estimated EFT is in the range of 900–1000 °C. The third fabric, F3 (OLL001 and MRB013), shows the decomposition of illite-muscovite and gehlenite, pointing to an EFT estimated at over 1000–1050 °C. Moreover, both individuals exhibit a yellowish colour (Fig. 9a, MRB013), typical of overfired calcareous ceramics, which also agrees with the decomposition of hematite.

Fig. 9
figure 9figure 9

a Photographies of representative ceramics for each one of the Cordoban reference groups. b Drawings of representative ceramics for each of the Cordoban reference groups, corresponding to photographs in (a). Drawings for individuals MRB010, 021, and OLL007 are not provided as the fragments correspond to an undefined part of the vessel

The calcareous group CGCRV03 accounts for 26 individuals scattered in 6 different fabrics. Fabric F1 (MRB0011, 017, CAY015 and 017) exhibits typical firing phases in calcareous ceramics (pyroxene and, especially, gehlenite) and illite-muscovite (including the d(002) peak at 10 Å). The estimated EFT is 850–950 °C. Fabric F2 (OLL006, 020, 029, 030, MRB006, 022, 025, 027, CAY010, 013, 014, 028, CRB011 and 026) is differentiated by the frequent presence of intense peaks of plagioclase and the constant absence of the d(002) peak at 10 Å of illite-muscovite. Thus, the estimated EFT is in the range of 950–1000 °C. The individual MRB012 (F3) exhibits the total decomposition of illite-muscovite. The presence of gehlenite enables estimating the EFT in the range of 1000–1050 °C. The same EFT range is estimated for fabric F4, which only includes individual MRB024. This individual is unique because of its black colour (Fig. 9a, MRB024) due to the presence of magnetite, whose crystallisation points to an intentional reducing atmosphere (Maniatis et al. 1983; Maritan et al. 2005) that corresponds to a different technical solution for this ceramic. Fabric F5 (OLL010, 025, 026, 027 and CAY012) differs because of gehlenite decomposition, a metastable phase in calcareous ceramics (Heimann and Maggetti 2014). The estimated EFT must be slightly over 1050 °C, but these ceramics cannot be considered severe overfired. Finally, individual OLL028 (F6) exhibits the same mineral phases as the previous fabric, and its EFT must be estimated at the same range. Nevertheless, this individual exhibits (Fig. 8a) an intense peak at 9.14 Å (9.67°2θ) that seems to correspond to the d(020) peak (I % = 100) of stilbite-Ca (JCPDS #00-044-1479; (Na, K)Ca2Al5Si13O36·14H2O) a zeolite that could be a secondary phase. Other significant peaks of this mineral, d(13-2) (4.06 Å, 21.86°2θ; I % = 87) and d(15-2) (3.03 Å, 29.42°2θ; I % = 46), are placed in areas that overlap the plagioclase and the possible calcite, rendering complex to assure this identification.

Group CGCRV04, calcareous, includes 14 individuals distributed in four mineralogical fabrics. Fabric F1 (MRB003, CAY024 and 025) exhibits clear firing phases, pyroxene and especially gehlenite, and illite-muscovite (including the d(002) peak at 10 Å). The estimated EFT is in the range of 850–950/1000 °C. In contrast, fabric F2 (OLL012, MRB007, 030 and CRB007) do not show the d(002) peak at 10 Å of illite-muscovite, and the estimated EFT is in the range of 950–1000 °C. Fabric F3 (OLL014, MRB008, 016, 023 and 026) is characterised by illite-muscovite’s total decomposition and gehlenite’s presence, enabling estimating an EFT in the range of 1000–1050 °C. Finally, fabric F4 (MRB009 and CAY011) shows the total decomposition of gehlenite. Therefore, the estimated EFT is over 1050 °C.

Finally, group CGCRV05 is the most calcareous local group and includes 18 individuals scattered in 3 fabrics. Fabric F1 (OLL004, 007, 008, CAY027 and 029) exhibits clear firing phases and illite-muscovite, enabling estimating the EFT in the range of 850–950/1000 °C. In contrast, fabric F2 (OLL016, 023 and MRB018) show the absence of the d(002) peak at 10 Å of illite-muscovite. The estimated EFT is in the range of 950–1000 °C. The fabric F3 (OLL018, 019, 024, CAY009, 016, 018, 022, 023 and 026) is, by far, the most represented. While exhibiting gehlenite, the illite-muscovite is decomposed, enabling estimating an EFT in the range of 1000–1050 °C. Finally, individual CAY030 differs from F3 because of vaterite (Fig. 8b), a rare calcium carbonate polymorph that has been previously reported in early modern ceramics (Iñañez 2007; Dias et al. 2012) and that could be present in individuals OLL008 and CAY027 (F1). The presence of vaterite is of a secondary origin from a Ca-rich wet environment (Pradell et al. 2010).

Concerning the Sevillian importations, all individuals are calcareous, and they have been grouped in ten different fabrics. The fabric F1 (OLL005 and 011) does not exhibit any clear firing phase, and the EFT can be estimated below 800/850 °C. The fabric F2 (MRB001, 002, 015 and CRB030) exhibits pyroxene and gehlenite as clear firing phases. Moreover, the absence of the d(002) peak at 10 Å of illite-muscovite enables estimating the EFT at 950–1000 °C. Two individuals of this fabric (MRB001 and CRB030), one individual in fabric F4, and two in fabric F5 could exhibit andradite, a garnet, but its identification is unsure. Individual MRB019 exhibits (Fig. 8c) the same fabric as F2 but with the presence of aragonite, a calcium carbonate polymorph of clear secondary origin, defining fabric F3, whose EFT is also in the range of 950–1000 °C. The fabric F4 (CAY001, 019, 021, CRB003, 018, 019 and 020) differs from fabric F2 because of the total decomposition of illite-muscovite, enabling estimating the EFT in the 950/1000–1050 °C range. The fabric F5 (OLL021, 022, MRB014, CAY002, 003, 005, 007, CRB001, 002, 017 and 023) is the largest fabric for Sevillian ceramics in Córdoba and differs from fabric F4 because of analcime, an authigenic sodic zeolite (Na(AlSi2O6)·H2O). The estimated EFT is in the range of 950/1000–1050 °C, which, for calcareous ceramics, can be considered a non-severe overfiring. At this stage, it is common to observe that these ceramics have undergone a double process of alteration that possibly implies, in a first step, the alteration of the glassy phase already developed. This alteration typically enables the lixiviation of potassium and rubidium that are thus depleted in these ceramics. In a second step, analcime crystallises on the altered glassy phase incorporating allochthonous sodium, enriching its initial concentration (Buxeda 1999; Buxeda et al. 2002; Schwedt et al. 2006). Indeed, some of those individuals (especially CAY005) exhibit the highest concentration of Na2O and the lowest of K2O (Table 3), resulting, most probably, from such alteration processes. The individual CAY020 (fabric F6) exhibits the same mineralogy by XRD plus vaterite, another secondary phase, and the EFT is estimated at 950/1000–1050 °C. A similar situation happens to individual CAY008 (fabric F7) with the mineralogy of fabric F5, but exhibiting stilbite, another secondary phase, and having the same EFT. The fabrics F8 (OLL015 and 017) and F9 (CAY006), in contrast to fabric F5, do not exhibit hematite, but they contain andradite and haüyne (Fig. 8d). The latter phase belongs to the sodalite group and corresponds to an intense peak at 3.72 Å (23.89°2θ) that seems to be its d(211) peak (I % = 100) (JCPDS #01-078-2490; Na4Ca2Al6Si6O22S2(SO4)Cl0.5). Individual CAY006 also exhibits low intense peaks of analcime. The EFT estimated for fabrics F8 and F9 is 950/1000–1050 °C. The last Sevillian fabric, F10 (CRB013), is similar to fabric F5 without hematite and gehlenite. The estimated EFT is over 1050 °C.

Regarding the importations from Granada, the calcareous group CGGRA, the 5 individuals are classed in two different fabrics. Fabric F1 (CRB004, 005, 008 and 022) exhibits the presence of clear firing phases, pyroxene and gehlenite, together with illite-muscovite enabling estimating the EFT at the 850–950/1000 °C range. Fabric F2 (CRB021) only differs because of analcime, enabling estimating the EFT in the same range as F1.

If we turn now our attention to the groups of unknown origin, the low calcareous group CGNC01 shows four different fabrics. The fabrics F1 (CRB012) and F2 (CRB025, 027 and 028) do not exhibit any clear firing phase. Since low calcareous ceramics undergo few mineralogical changes, the EFT can only be estimated below 900/950 °C. The difference between both fabrics is the possible presence of talc in individual CRB012, a mineral phase that dehydorxylates between 800 and 895 °C (Liu et al. 2014). The other three individuals correspond to fabrics F3 (CRB010) and F4 (CRB009 and 014), exhibiting clear firing phases besides the decomposition of illite-muscovite. The estimated EFT is above 950/1000 °C. In fabric F3, hematite and spinel can be observed, pointing to an oxidising environment, while in fabric F4, the presence of hercynite (Fig. 8e; Fig. 10a, CRB009) indicates a strong reduction environment at high temperatures.

Fig. 10
figure 10figure 10

a Photographies of representative imported ceramics recovered in the city of Córdoba. b Drawings of representative imported ceramics recovered in the city of Córdoba, corresponding to photographs in (a). Drawings for individuals CRB013, and 016 are not provided as the fragments correspond to an undefined part of the vessel

All individuals in the calcareous group of unknown origin CGNC02 belong to one fabric, F1 (CAY004, CRB006 and 024). The estimated EFT is in the 950/1000–1050 °C range due to the absolute absence of illite-muscovite and the presence of gehlenite.

Finally, focusing on the three loners, we can see that the calcareous individual OLL009 must have an EFT estimated over 950/1000 °C due to the decomposition of illite-muscovite. On the contrary, the calcareous individual CRB015 shows lower EFT (850–950/1000 °C) because of illite-muscovite and clear firing phases, especially pyroxene and gehlenite. The individual CRB016 is an entirely different case (Fig. 8f). This individual is porcelain, implying a completely different technological solution in ceramic products. The presence of mullite, cristoballite and corundum enables estimating an EFT of 1200/1300 °C.

In summary, we can highlight all the ceramic sherds, except individuals MRB024 (calcareous group CGCRV03, fabric F4) and CRB009 and 014 (low calcareous group CGNC01, fabric F4), appear to be fired under mainly oxidising atmospheres.

Considering the local products, low-calcareous groups tend to have lower EFTs than the calcareous ones and those individuals showing higher EFTs (> 950/1000 °C) generally correspond to kiln elements and glazed ceramics. Calcareous groups show a very different range of temperatures, from 800 to 850 °C to above 1050 °C, without a clear difference between glazed and unglazed ceramics. Although corresponding to production centres, only two sherds (OLL001 and MRB013, group CGCRV02c, fabric F3) can be considered overfired. However, as expected, most elements of kiln furniture show high EFTs. Finally, it must be highlighted that the only two examples of tin-lead glazed vessels produced in Córdoba (group CGCRV05: OLL023 (Fig. 9a), fabric F2, and CAY009, fabric F3) have an EFT between 950–1000 and 1000–1050 °C.

If we turn our attention to the imports, Sevillian ceramics are mainly tin-lead glazed individuals with high EFTs between 950/1000–1050 °C. Some differences in the mineral composition can be observed as they come from different reference groups. Nevertheless, the homogeneity in the temperatures proves a good knowledge of the technical process. Lower EFTs correspond to unglazed sherds, even if an example of an overfired ceramic has been identified in CRB013, a green-glazed bowl. Imports from Granada are also very homogeneous (EFT between 850/950–1000 °C in all cases), and the same can be stated for ceramics corresponding to the groups CGNC01 and CGNC02, demonstrating the quality of the imported products.

Discussion

Integrating the results of the archaeometric analysis with the archaeological evidence, we can observe that the defined local reference groups (Fig. 9a and b) have a chronological and functional coherence. From the fourteenth to the sixteenth centuries, four different calcareous reference groups are documented (X̅CaO in chronological order: CGCRV03 –6.66%–, CGCRV05 –19.12%–, CGCRV04 –11.15%–, CGCRV02c –8.10%–), while we only detect the presence of low calcareous products at the sixteenth, or even fifteenth, century (X̅CaO in chronological order: CGCRV01 –1.15%–, CGCRV02 –2.36%–) (Table 4).

The calcareous group CGCRV03 (26 individuals) corresponds to the fourteenth–fifteenth centuries. This group integrates calcareous coarse ware (unglazed and honey glazed), storage and transport jars (unglazed and honey glaze), cooking pots (Fig. 9a and b, CRB026) and kiln furniture (one saggar, Fig. 9a and b, MRB012). Among this group’s products, we must highlight the presence of glazed ware that exhibits honey or honey/brown glaze at the interior and dark/black glaze at the exterior (OLL027, 030, MRB006, CAY012 and 013) (Fig. 9a and b, CAY012). The combination of two different colours for the interior and exterior of the glaze is a characteristic already in the Islamic pottery production of Córdoba (Salinas and Pradell 2018). Even if there are also ceramics of this group exhibiting a uniform dark/brown (OLL25 and 29) glaze or honey/brown (OLL026, 029 and CRB026) glaze in both sites, the individual CRB007 (from group CGCRV04) also shows this combination of two different colours in a consumption centre. This evidence suggests that the existence of ceramics with honey or honey/brown glaze at the interior and dark/black glaze at the exterior is intentional. Another interesting group of ceramics corresponds to plates (CAY028) and dishes (OLL010, CAY014, 015 and 017) with manganese decoration on honey glaze, also present in group CGCRV04 (dishes OLL012, 014) (Fig. 9a and b, OLL012). MRB024, a basin, is one of few ceramics fired under a reducing atmosphere (Fig. 9a and b). Finally, as expected in a production centre, some individuals are discarded waste. Thus, some of the coarse ware vessels are just biscuit pottery not yet glazed, while some of the bowls show holes in the bottom because of the breakage of their thinner parts.

The group CGCRV05 (18 individuals) seems to start in the fifteenth century, even if two individuals (CAY016 and 018) have a broader possible chronology in the fourteenth–fifteenth century. Nevertheless, the chronology given to these two individuals corresponds to a general approximation since the archaeologists did not find evidence suggesting a more tight chronology. Because of that, these two individuals have not been considered to establish an earlier chronology for the group. This group contains unglazed coarse ware, green glazed coarse ware, some storage and transport jars (Fig. 9a and b, CAY030 and OLL007) and some trivets (OLL018, 019 and CAY018). This group also contains the only two examples of tin-lead glazed sherds produced in the city of Córdoba: a bowl glazed in plain white (blanca lisa) (CAY009) and another one of Isabella Polychrome (azul y morado), decorated in blue and manganese on a white background (Fig. 9a and b, OLL023). Interestingly, there was no evidence of tin-lead glazed ceramic production in Córdoba, and ceramics of this kind recovered in the city were mainly thought to have come from Seville. The high CaO content of this group, the highest in the Cordoban products, could be explained by the attempt to produce tin-lead glazed vessels. Local products have only been identified in this group, and the CaO content seems to drop in the products that follow, once tin-lead glaze manufacture was possibly disregarded. Another interesting case is CAY016 (Fig. 9a and b), which exhibits two different glaze colours, with turquoise blue in the interior and green in the exterior. Finally, CAY023 corresponds to a flowerpot, a ceramic type most probably inspired by Islamic ceramics (Barceló and Rosselló 1996) that was very successful in the Late Middle Ages and the early modern period in cultivating basil and other culinary spices (Serra 2021).

The group CGCRV04 (14 individuals) is active in the fifteenth–sixteenth century, but as in the previous group, one individual (CAY011) also exists with a broader possible chronology in the fourteenth–fifteenth century. The group comprises coarse ware (green glazed and unglazed) (Fig. 9, MRB011 and 003) and trivets (MRB016 and 023) (Fig. 9a and b, MRB023). This group shares with CGCRV03 the existence of honey/brown glaze at the interior and dark/black glaze at the exterior (CRB007), and honey glaze with manganese decorations (OLL012, 014) (Fig. 9a and b, OLL012). Finally, one individual also has a yellow glaze on the interior and green on the exterior (Fig. 9a and b, MRB026), representing this tradition of two different colours in the glaze again.

The last calcareous group, CGCRV02c (4 individuals), is related to the low calcareous CGCRV02 (3 individuals) but contains higher levels of CaO. These two groups seem to be contemporary to the low calcareous group CGCRV01 (6 individuals), whose chronology must be centred to the sixteenth century, even if Avenida Ollerías, 14 site has been roughly dated back to the fifteenth century. This rough chronology affects the three groups, including a few individuals from this site. These three groups comprise kiln furniture (CGCRV02c, the kiln rods OLL001 and 003; CGCRV02, the kiln rod OLL002; CGCRV01, the trivet MRB029) (Fig. 9a and b, OLL003), glazed (Fig. 9a and b, MRB004 and MRB005) and unglazed (Fig. 9a and b, MRB013 and MRB010) coarse ware (including a cheese dish, Fig. 9a and b, OLL013), and one cooking pot (Fig. 9a, MRB021).

Although Córdoba cannot be thought of as a massive production centre, some products manufactured there have been found in other areas in the South of the Iberian Peninsula. During the comparison with our data bank, we identified two ceramics, PRI011 and VLM040, belonging to the CGCRV05 reference group (Fig. 5). The individual PRI011 corresponds to a dish decorated with an interior yellow glaze and an exterior green glaze (similar to Fig. 9a and b, MRB026, group CGCRV04) recovered in a context of the seventeenth century found in the city of Priego de Córdoba, in the border between the kingdoms of Granada and Córdoba. Therefore, we can infer that glazes of two colours were also manufactured in group CGCRV05, even if not detected in Córdoba itself. The individual VLM040 is an unglazed pitcher found in the town of Villamartín, in the area of Cádiz (in Western Andalusia), in a context roughly dated from the fifteenth to the seventeenth centuries. Along these lines, we must highlight that no similarities have been observed with the transport jars of hypothesised Cordoban origin recovered from the Tortugas shipwreck (Hughes 2014).

As expected, most of the importations (Fig. 10a and b) have been found in the consumption centre of Casa Carbonell, although some of them have been profusely recovered in several Cordoban workshops too. Sevillian imports (CGSEV) have been found in all archaeological sites, both production and consumption centres. Group CGSEV represent 25.83% of the individuals sampled in Córdoba (31 out of 120), going up to 33.33 % in Casa Carbonell (10 out of 30), the only consumption centre. These figures demonstrate a remarkable dependence on this production centre during the late medieval and early modern periods. Although most of the ceramics imported from Seville are tin-lead glazed vessels, some examples of transport jars, storage vessels and coarse ware individuals have been identified. Coarse ware imports contain both unglazed and glazed individuals, including an unglazed basin (Fig. 10a and b, OLL005), a salt-cellar (OLL011) and a bowl (MRB019) (all these from the fifteenth–sixteenth centuries), as well as a green-glazed bowl (Fig. 10a, CRB013) (dated back to the seventeenth–eighteenth centuries). Regarding transport and storage jars, two examples of storage jars (MRB001 and 002) and a water container (Fig. 10a, CRB030) have been identified (sixteenth–eighteenth centuries). Regarding tin-lead glazed ceramic imports, a great variety of forms and decorations have been found in Cordoban archaeological sites dating from the fourteenth to eighteenth centuries, proving the well-established tradition of tin-lead glaze production in Seville and its distribution. The most ancient examples of tin-lead glazed vessels correspond to a bowl (Fig. 10a and b, CAY001) and a basin (CAY019) decorated in manganese on white (fourteenth–fifteenth centuries). Other types are also present: (i) a bowl or dish (CAY003) and a plate presenting Sevilla blue on white decoration (azul sobre blanco) (fourteenth–sixteenth centuries) (Fig. 10a and b, CAY020); (ii) a bowl decorated in lusterware and blue (loza dorada y azul) (Fig. 10a and b, OLL021) (fifteenth century); (iii) 3 dishes (Fig. 10a and b: OLL017; 022 and CAY002) and a bowl or dish (CAY006) of Santo Domingo blue on white (azul figurativa) (fifteenth–sixteenth centuries); (iv) plain whiteglaze (blanca lisa), which is the most common abundant, in bowls (Fig. 10a and b: OLL015; CAY021 and CRB023), dishes (CAY005 and 007) and plates (CAY008) (fifteenth–eighteenth centuries); (v) three examples of blue and green basins (MRB014, 015 and Fig. 10a and b, CRB003) (sixteenth–eighteenth centuries); (vi) 3 dishes (CRB001, 018 and 020) and a bowl (CRB017 and Fig. 10a and b, CRB019) presenting Yayal blue decoration (azul lineal) (seventeenth–eighteenth centuries); and, finally, (vii) a green and white bowl (verde sobre blanco) (Fig. 10a and b, CRB002) (seventeenth–eighteenth centuries). As said before, Sevillian imports form a vast group corresponding to several reference groups. Nevertheless, most ceramics show an estimated EFT between 950/1000–1050 °C (coherent with the technical requirements of this kind of pottery), while estimated EFTs below 1000 °C tend to correspond to other kinds of ceramics like coarse ware or transport and storage vessels.

Imports from Granada (CGGRA) have only been identified in Casa Carbonell consumption centre and are characterised by showing important concentrations of Fe2O3 (X̅ = 6.40%, Table 4) and Al2O3 (X̅ = 17.31%). These concentrations are typical of the chemical composition of Granada, as observed in an ongoing study of the production centres in this city. Technically, this group is homogeneous, containing only two fabrics with an estimated EFT between 850 and 950/1000 °C. As a distinctive feature of the ceramics produced in Granada, it must be noted that illite-muscovite peaks do not disappear, although clear firing phases such as pyroxenes and gehlenite, together with secondary phases such as analcime, can be observed (Table 5). That is explained by the characteristic metamorphic geology of the area of Granada, which is extremely rich in phyllite and schists providing abundant micas to the ceramic paste (Carvajal and Day 2015). Archaeologically, the imports from Granada recovered in Córdoba are mainly tin-lead glazed vessels dating from the seventeenth to the eighteenth centuries. In particular, an unglazed dish (CRB008), a plain white dish (CRB004) and a plain white bowl (Fig. 10a and b, CRB005). Also, two examples of bowls decorated with blue leaf motifs (Garzón 2004: 477, Fig. 468) correspond to the traditional local production of Fajalauza (CRB021 and Fig. 10a and b, CRB022). All these ceramics belong to a unique reference group related to el Realejo quarter, one of the main production areas in the city of Granada. According to ongoing studies about ceramic production in Granada, this workshop would be active from the fifteenth to the eighteenth centuries, demonstrating continuity between the Nasrid and the Christian periods in ceramic manufacture. However, we have not identified imports from Granada before the seventeenth century.

Low-calcareous group CGNC01—only found in Casa Carbonell consumption centre—comprises 5 glazed dishes and 2 glazed bowls showing high levels of MnO (X̅ = 0.24%, Table 4), and its origin is still unknown. It is interesting to note that, even their general homogeneity, some differences in the colour of their pastes and glazes can be appreciated. That phenomenon could be explained because of the differences in their mineralogic composition (Table 5). While most individuals exhibit reddish-brown pastes and honey-brown glazes (Fig. 10a and b, CRB028), individuals CRB009 and 014—from fabric F4—exhibit dark-grey pastes and deep-green glazes (Fig. 10a and b, CRB009). Mineralogically, some of the reddish-brown pastes contain hematite in their composition due to a primarily oxidising firing (CRB010 and, possibly, CRB028). Nevertheless, this mineral phase cannot be found in dark-grey pastes, which may be related to a reducing firing, as reflected by maghemite in CRB014 and hercynite in both individuals, and the diffusion of Fe2+ ions into the glaze must cause the colour of the glazes. Thus, primarily oxidising firing produces reddish pastes and honey-brown glazes, while reducing firing produces dark pastes and green glazes (Molera et al. 1997). Nevertheless, these evident colour differences in such a homogeneous set of imported ceramics are difficult to explain from the customer’s point of view.

Chemical group CGNC02 has been identified in Casa Carbonell consumption centre and the Hornos de San Cayetano workshop. This group is by far the most calcareous one in this study (X̅ = 30.09%, Table 4), and its provenance cannot be identified at the moment. This group comprises three plain white glazed bowls dating from the modern period (Fig. 10a and b, CRB024). All the individuals are technically homogeneous as they correspond to a unique fabric (F1). The estimated EFT for this entire group is considerably high (950/1000–1050 °C), as corresponds to tin-lead glazed ceramics, demonstrating an important knowledge of the manufacturing process for this kind of ceramics.

Finally, three individuals could not be linked to any reference group. These loners are a green-glazed bowl (Fig. 10a and b, OLL009), a coarse ware handle (Fig. 10a and b, CRB015) and a porcelain sherd (Fig. 10a, CRB016).

According to the archives, the first porcelains arrived in Europe from China between the fifteenth and the seventeenth centuries, during the Ming dynasty (1368–1644). These porcelains were, at first, imported for the Portuguese market, and they arrived in the Castilian Crown during the Habsburg period (Dias et al. 2013; Krahe 2014). Concerning their characterisation, instrumental neutron activation analyses (INAA) show important amounts of Na2O (X̅ = 1.25%) and K2O (X̅ = 3.35%)—and low quantities of Fe2O3 (X̅ = 1.19%)—for Chinese porcelains arriving in Portugal during this period (Dias et al., 2013). High concentrations of Na2O and K2O are necessary as fluxes, while low quantities of Fe2O3 and TiO2 are needed to obtain white bodies. Nevertheless, individual CRB016 does not correspond to the characteristics of these porcelains, as Na2O and K2O compositions are lower in this sample (0.34% and 1.31%, respectively). The chemical composition of CRB016 would match better with some examples of porcelain produced during the previous Sui-Tang (581–907) and Song-Yuan (960–1368) dynasties. Their compositions have been determined by XRF analyses (Na2O, X̅ = 0.37%, and K2O, X̅ = 1.62%). However, Fe2O3 and Al2O3 quantities are higher in this kind of porcelain (Fe2O3, X̅ = 1.29% and Al2O3, X̅ = 29.47%) (Leung et al. 2000) than in individual CRB016 (Fe2O3 = 0.84%, and Al2O3 = 23.97%). The same occurs if we compare individual CRB016 with other examples of coarse white porcelains dated from the Sui-Tang period (Lu et al. 2012) and with several proto-porcelains recovered from Pre-Qing archaeological contexts (before 1644) (Wu et al. 2009). Because of its exceptionality, the provenance of CRB016 cannot be identified. Nevertheless, its chronology is determined by the archaeologists in the seventeenth–eighteenth centuries. Technically, the low values of flux elements make us think that individual CRB016 reached very high temperatures, estimating its EFT above 1200/1300 °C.

The distribution of the sampled archaeological sites according to the defined groups has been studied by employing correspondence analysis. The resulting biplot (Fig. 11) explains 94.9% of the total inertia and shows a clear differentiation between the production sites to the left and the consumption centre of Casa Carbonell to the right. The former attracts the local reference groups, while the latter attracts all the imports and loners, but Sevillian ceramics are placed in a middle position. This differentiation is significative—χ2 (30, n = 120) = 88.792, p = 1 × 10−6—and reflects that, except for Sevillian products, almost all other importations and loners have been recovered at Casa Carbonell. Moreover, it also appears that Casa Carbonell does not consume a significant number of local products (just 4 out of 30) (Table 2). On the left side, we can also observe a differentiation between groups CGCRV03 and, especially, CGCRV05, attracted by Hornos de San Cayetano and Avenida Ollerías, 14, and all other groups, attracted by Ronda Marrubial. Excluding Casa Carbonell, the loners and all imports except from those coming from Seville, differentiation is also significant—χ2 (12, n = 88) = 22.37, p = 0.034—showing a trend that links the older groups (fourteenth–fifteenth centuries) to the production sites of Hornos de San Cayetano and Avenida Ollerías, 14, while, the later ones (fifteenth–sixteenth centuries) with Ronda Marrubial.

Fig. 11
figure 11

Biplot of the correspondence analysis between the archaeological sites sampled (in blue) and the reference groups defined (in red). OLL: Avenida Ollerías, 14; CAY: hornos de San Cayetano; MRB: Ronda Marrubial; CRB: Casa Carbonell

Conclusions

The present study has enabled us to define the widely known Cordoban ceramic production between the late medieval and early modern periods and study some aspects of the change-continuity phenomenon regarding the previous Islamic times. Moreover, the importations in Córdoba are evidence of the relations between this city and its nearest kingdoms. Finally, it has been proved how some Cordoban products were arriving in other areas of both Kingdoms of Córdoba (Priego de Córdoba) and Seville (Villamartín, Cádiz), but no evidence of Cordoban imports to the Americas has been found.

Local production and imports during the modern period

Although three production centres have been sampled (Avenida Ollerias, 14, Ronda Marrubial and Hornos de San Cayetano), no significant differences have been identified regarding the type of pottery manufactured in each workshop. Nevertheless, some tendencies have been noticed regarding the chronology of the ceramics, being Hornos de San Cayetano and Avenida Ollerías, 14 more active in the fourteenth–fifteenth centuries, and Ronda Marrubial workshop in the fifteenth–sixteenth centuries. Nevertheless, the proximity of the three workshops does not allow to rule out the possibility that all of them were part of a larger complex located in the Barrio de las Ollerías.

Concerning the local production in Córdoba, six reference groups have been defined: CGCRV01, CGCRV02, CGCRV02c, CGCRV03, CGCRV04 and CGCRV05. The pottery produced in these workshops shows differences mainly related to CaO and Sr content (Table 4). These differences could be related to the information given by the archives (Córdoba de la Llave 1990: 325-326), which underline the existence of two different types of potters. On the one hand, the olleros produced mainly cooking ware by using unmixed clays from different outcrops. According to the 1529 ordinances, these clays were collected from Valdeleche and Rabanales meadows, but in 1545 the ordinances explain how the activity moved to Guajardo domain, of better quality. These clays possibly correspond to the barro bermejo (red clay) that, according to the archives, was used for cooking ware. On the other hand, the tinajeros produced transport and storage jars. All ceramics not intended for cooking wares were made by mixing red clays and barro blanco (white clays), a yellowish clay producing buff colours after firing. Transport and storage jars seem to have been produced by mixing one part of red clay and five parts of white clay, while dishes, jars and other utilitarian wares used two parts of red clay and one part of white clay. Assuming that our group CGCRV01 represents one of these red clays, we have performed a simple calculation assuming that group CGCRV05 corresponds to combining five parts of white clay with one part of red clay. In this way, even if we do not know the initial composition of the white clay, group CGCRV05, clearly dominated by it, is its best close approximation. Using the means of these groups in a two parts proportion of group CGCRV01 and one part of group CGCRV05, we obtain calculated means for this mixture that closely conform to the means of group CGCRV03 (Table 4). All calculated values are close to the observed means of this group within one standard deviation (only MgO deviates + 1.5 standard deviations). Thus, the defined reference groups for Córdoba seem to agree with the archive information on pottery production in this town. The difference in the CaO content could at least refer to the distinction between red (CGCRV01 and CGCRV02) and white clays (CGCRV03, CGCRV04 and CGCRV05) with mixtures at different proportions. Concerning calcareous groups (CGCRV02c, CGCRV03, CGCRV04 and CGCRV05), the differences in the CaO content seem to be related to the kind of pottery produced: honey-glazed coarse ware tends to be related to less calcareous compositions and green-glazed coarse ware to more calcareous compositions. It is important to highlight that large storage and transport jars mostly belong to group CGCRV05, the most calcareous one. Finally, neither historical documentation nor archaeological studies mention tin-lead glazed ceramic production at Córdova. However, we have identified such products in group CGCRV05: OLL023 (Fig. 9a and b) (Isabella polychrome, or azul y morado, bowl) and CAY009 (Plain white, or blanca lisa, bowl). Due to their exceptionality and low quality may be interpreted as tests, but we cannot discard that tin-lead glazed vessels were really produced.

About the imports found in Córdoba, it must be remarked that Sevillian ceramics were present in the city during all the medieval and modern periods, becoming the principal provider of tin-lead glazed vessels at Cordoba. This situation shows Córdoba's political and economic dependence on Seville since the Christian conquest and the role of Seville as the main production centre of tin-lead glazed ceramics in Europe during the Modern Era. Nevertheless, since the seventeenth century, importations from Granada (mainly plain white and Fajalauza tableware) and the unknown groups CGNC01 and 02 (this could also be present from the fifteenth century) started appearing in Córdoba.

Influence of the Islamic tradition

This study has also given information about the Islamic cultural legacy in the late medieval and early modern Cordoban ceramic production. In this sense, several honey-glazed plates and dishes presenting organic and geometric decorations in manganese have been studied (OLL010, 012–Fig. 9a–and 014; CAY014, 015, 017 and 028). The decorations are usually placed around the border, although sometimes they appear as central motifs. Manganese on honey designs like those has only been studied for Seville as a decoration from the Islamic tradition (Amores and Chisvert 1992, p. 290). In the case of Córdoba, the analyses conclude that manganese on honey ceramics found in the city correspond to local productions related to reference groups CGCRV04 and CGCRV05. The local examples found in Córdoba may also have an Islamic origin, as an inheritance of the first glazed productions identified in the caliphal palace complex of Madīnat al-Zahrā. The manufacture of manganese on honey vessels during the Christian period has been related to the Moorish potters (Córdoba de la Llave 1997, p. 354). In the framework of this PhD Thesis, other examples of manganese on honey dishes and plates have also been sampled in different archaeological sites of the Kingdom of Granada (Granada and Castillo de Montejícar), responding to local productions too. That would mean that it was a decoration that originated in the Early Middle Ages and was still used during the Late Middle Ages and the early modern period, not only in the city of Seville but also in other points of the current region of Andalusia. In addition, many bichrome individuals (showing combinations of honey and dark brown, green and yellow-honey and turquoise-blue and green surfaces in the same individual) have been identified as local productions, too (CGCRV03, 04 and 05 reference groups, Fig. 9a CAY012, MRB026 and CAY016). These bichrome products were also found in other places (PRI011 to Priego de Córdoba). The combination of yellow and green glaze has been identified in Córdoba as a distinctive local production since the very first times of the Islamic occupation, during the Emirate period (eighth–tenth centuries), although the production of glazed ceramics in al-Andalus did not start until the late ninth century at the earliest (Salinas and Pradell 2018). Finally, the Islamic legacy is also present in the ceramic types. Thus, the Christian Cordoban plates show a clear continuity with the previous Islamic ataifor (Amores and Chisvert 1992, p. 290), serving bowls used for collective eating without individual dishes. During the Christian period, the ataifor is kept, but just as a serving plate, and individual dishes and bowls appear. Another continuity is observed in the presence of flowerpots, a ceramic type that originated in the Islamic period. Finally, some kiln furniture—like kiln rods—has been identified in early modern stratigraphic contexts, showing a relationship with the Islamic world, where these kinds of kilns originated.

Although almost 300 years had elapsed since the Christian conquest of the city, there existed still an evident legacy of the Islamic material culture in Modern Córdoba. Thus, the cultural context of ceramic production in Córdoba considerably differs from other close cities like Seville. In this case, the commercial expansion of the Castilian Crown after the conquest of the Americas turned Seville into the most important ceramic production and distribution centre in Europe, where craftsmen from all over Europe established their workshops. For example, some of the most important ceramists in Seville in this period were the Italian potters Niculoso Pisano and Tomás Pesaro (Buxeda et al. 2015). Consequently, Seville became a reference point in the manufacture of tin-lead glazed vessels, a symbol of the European Renaissance. In this sense, Seville can be considered a dynamic city, open to global trade and influenced by the new ideas and aesthetics emerging in all of Europe. On the contrary, Córdoba, even if integrated into the broader network since the Christian conquest that will be the centre of the Atlantic expansion, could instead have a role as a part of the hinterland and a region more enclosed within itself compared to the Atlantic commercial cities. Córdoba became a regional ceramic production centre that received less immigration and fewer external influences. Thus, traditional production techniques and ceramic forms inherited from the Islamic times remained. To summarise, the cases of Seville and Córdoba illustrate how two close cities conquered at the same time (1236 for Córdoba and 1247 for Seville) developed different social and cultural traits because of their different economic and demographic contexts. Moreover, this example also shows how the ceramic products reflect these realities, as material culture cannot be studied without knowing the social, cultural and historical context of the people who manufactured and used the objects.

Continuity of the research

The future research in this city and the other archaeological sites sampled in this Doctoral Thesis project will help us identify their role as both production and distribution centres. The next step in the research, which is already in progress, is the evaluation of the technical aspects using Optical Microscopy and Scanning Electronic Microscopy. For example, the characterisation of glazes and pigments used for the decorations, to know more about the complex world of the activity of making pottery during this period. This knowledge will be used to learn more about the transition between the Islamic period and Christianisation, identifying the elements that remained and those that were substituted along the time, providing information about the cultural and technological change in a modern society with an important Islamic medieval legacy.