Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

North and South in Medieval Iberia: A historical and environmental estimate through isotopic analyses

  • José Francisco Martín-Alonso ,

    Contributed equally to this work with: José Francisco Martín-Alonso, Sylvia A. Jiménez-Brobeil

    Roles Data curation, Formal analysis, Investigation, Methodology, Writing – original draft

    Affiliation Department of Legal Medicine, Toxicology and Physical Anthropology, University of Granada, Granada, Spain

  • Zita Laffranchi ,

    Roles Investigation, Writing – review & editing

    ‡ ZL, MM, LCB and LAMS also contributed equally to this work.

    Affiliation Department of Physical Anthropology, Institute of Forensic Medicine, University of Bern, Bern, Switzerland

  • Marco Milella ,

    Roles Supervision, Writing – review & editing

    ‡ ZL, MM, LCB and LAMS also contributed equally to this work.

    Affiliation Department of Physical Anthropology, Institute of Forensic Medicine, University of Bern, Bern, Switzerland

  • Lorenza Coppola-Bove ,

    Roles Investigation, Writing – review & editing

    ‡ ZL, MM, LCB and LAMS also contributed equally to this work.

    Affiliation Department of Legal Medicine, Toxicology and Physical Anthropology, University of Granada, Granada, Spain

  • Luis A. Mena-Sánchez ,

    Roles Software

    ‡ ZL, MM, LCB and LAMS also contributed equally to this work.

    Affiliation Department of Legal Medicine, Toxicology and Physical Anthropology, University of Granada, Granada, Spain

  • Sylvia A. Jiménez-Brobeil

    Contributed equally to this work with: José Francisco Martín-Alonso, Sylvia A. Jiménez-Brobeil

    Roles Conceptualization, Funding acquisition, Investigation, Project administration, Writing – original draft

    jbrobeil@ugr.es

    Affiliation Department of Legal Medicine, Toxicology and Physical Anthropology, University of Granada, Granada, Spain

Abstract

The Middle Ages in the Iberian Peninsula is a period of special interest for studying the relationship of climate change with historical and socioeconomic processes. Between the 8th and 15th centuries AD, the Peninsula was characterized not only by complex political, cultural, and social transitions but also by major variations in the climate. The objective of this study was to examine differences in diet and mobility between distinct populations of the Peninsula and explore the possible relationship of diet, mobility, and culture with environmental variables and geographical settings. For this purpose, we obtained stable isotopic ratios of carbon and oxygen (δ13C and δ18O) from the enamel apatite of first upper incisors from 145 individuals at eight archeological sites that represent both Christian and Islamic communities and both rural and urban social settings. Results revealed a dietary difference between Christian and Islamic populations, observing a greater contribution of C4 plants, possibly sorghum, in the diet of the latter, especially in a rural setting. The disparity in oxygen isotopic ratios between populations from the North and South of the Peninsula is consistent with modern climatic differences between these regions. In this line, intraregional variability in oxygen isotopic ratios may hint at diachronic occupation phases under varying climatic conditions. The few isotopic outliers in our sample suggest overall low mobility levels.

Introduction

The Middle Ages (8th-15th centuries) in the Iberian Peninsula was an especially interesting period from multiple perspectives. Historically, it featured political occupation by Muslim groups and a long and complex period in which territory was recovered by different Christian kingdoms in the North of the Peninsula [1, 2]. From a cultural and social perspective, the Islamic arrival brought new habits and customs and novel techniques in craftwork and farming, with the introduction of new crops [3, 4]. This long chronological period also included climate changes, notably the Medieval Climate Anomaly (9th-11th century) and the Little Ice Age (14th-15th century), separated by a short transition phase in the 13th century [57]. However, there has been little investigation of the influence of these environmental events on cultural and social changes, especially in human remains, and further in-depth research is required.

One useful approach is offered by stable isotope analysis of the apatite in human tooth enamel [8]. Isotope analysis of bone can yield information on the last years of life of individuals [9], with results that vary according to the turnover rate of the bone under study. However, isotope analysis of tooth enamel is not affected by tissue remodeling [1012] but rather reflects the diet consumed during its formation [13]. Hence, the results obtained refer to years during which the dental crown forms or to a specific time point during this process, depending on the sampling technique. These features make the isotopic signal dental enamel a useful marker of the ingested food and water, and ultimately the environmental variables, characterizing the place where one individual spent their childhood. There it follows the wide application of isotopic analyses of dental enamel in mobility research to pinpoint the presence, and possibly geographic origin of nonlocal individuals [14]. One potential limit to this approach is, however, the effect played by breastfeeding and weaning on the observed isotopic values [15].

The proportion of stable carbon isotopes (13C/12C) in tooth enamel apatite corresponds to the whole diet, including proteins, carbohydrates, and fats, whereas the proportion in collagen is largely related to its protein component [1618]. Various authors have described the δ13Cen (VPDB) values associated with different types of diet [1922], with values close to -14‰ being characteristic of environments with C3 plants, those closer to 0‰ reflecting C4 plant intake, generally in warmer climates [23], and values between -9.5 and -12.8‰ suggesting a mixed diet of C3 and C4 plants. Analysis of the proportion of 18O/16O isotopes is also used by archeologists to track mobility patterns [14, 2426] because it varies geographically as a function of the sources of drinking water [26]. The isotopic proportion of body oxygen results from a complex development involving metabolic processes and specific factors such as body size [2729]. The main contributor to the isotopic representation of oxygen in the body is drinking water [30, 31], and δ18Odw values (dw = drinking water) are closely bound to this source [32, 33]. It should be noted that isotopic differences can be generated between local rainwater and water at a specific site due to its evaporation or travel through run-offs or streams, etc. [34, 35]. The isotopic proportion of drinking water is also influenced by climate factors [30, 36], and it therefore depends on multiple parameters, including latitude, altitude, season, precipitation level, temperature, and/or distance from the coast [25, 37].

Studies on the Iberian Peninsula during the Middle Ages have related tooth enamel isotopic values to diet and mobility patterns [24, 25, 3841], but there has been less research on their association with the environment. These aspects are all considered in the present study, with a particular focus on climate change. Two starting hypotheses were formulated: δ13Cen values would reflect dietary differences between Christians (in the North of the Peninsula) and Muslims (in the South) that can be attributed not only to cultural variations but also to geographic and environmental factors, as suggested by other studies based on collagen analyses (e.g., [24, 42, 43]); and δ18Odw values at each site would correspond to their geographic position and the chronology of their occupation and would also reflect climate changes experienced during the Middle Ages [6].

The main study objective was to determine possible differences in diet and climatic environment between Christian populations from the North of the Iberian Peninsula and Muslim populations from the South of the Peninsula. Secondary objectives were to detect possible territorial mobility patterns and to identify any dietary differences between social classes and between rural and urban dwellers.

Material and methods

The study included samples from 145 individuals at the Medieval sites depicted in Fig 1. Four sites are Christian rural villages from the North of the Iberian Peninsula, while four comprise two urban Muslim sites and two rural Muslim sites from the Southeast of the Peninsula. Table 1 exhibits their geographic coordinates, height above mean sea level (AMSL), and current climate according the Köppen-Geiger classification [44].

thumbnail
Fig 1. Geographical location of sites under study: 1.- Santa María de Tejuela; 2.- San Baudelio de Berlanga; 3.- El Castillo necropolis; 4.- La Olmeda; 5.- Sahl ben Malik cemetery; 6.- La Torrecilla; 7.- Talará cemetery; 8.- Mancoba.

Map: https://apps.nationalmap.gov/viewer/ (11/04/2024).

https://doi.org/10.1371/journal.pone.0304313.g001

thumbnail
Table 1. Archaeological sites and their geographic coordinates, altitude, and climate.

https://doi.org/10.1371/journal.pone.0304313.t001

Santa María de Tejuela (Bozoó, Burgos)

The remains of 182 individuals have been recovered from this cemetery (henceforth Tejuela) of a small rural community beside the Ebro River [45, 46]. Absolute dating values range from the late 8th century to the beginning of the 11th century, and it was mainly used between the mid-9th and late 10th centuries [47], i.e., during the Medieval Climate Anomaly [6, 7]. Samples were taken from 10 males and 10 females whose sex and age were previously estimated [47, 48].

San Baudelio de Berlanga (Berlanga de Duero, Soria)

At least 57 individuals have been recovered from the small cemetery of San Baudelio hermitage used alongside the 11th century [45, 49]. This small farm was mainly inhabited by stockbreeders with very hard conditions of life, supplied with water from a natural spring and the nearby Escalote River [50]. Individualized skeletons were dated from the 11th to mid-13th century, i.e., between the Medieval Climate Anomaly and the period of transition to the Little Ice Age [6, 51]. Samples were taken from 13 males and 7 females [51].

El Castillo necropolis (Palacios de la Sierra, Burgos)

Over 100 very poorly preserved skeletons have been recovered from the cemetery on a hill beside the Arlanza River (henceforth Palacios) [45, 52, 53]. The local economy, determined by the high altitude and climate, centered on stockbreeding and the exploitation of forest resources [5456]. According to epigraphs on the tombs and absolute dating values [53, 57], the cemetery was occupied from the 9th to 13th centuries, i.e., between the Medieval Climate Anomaly and the period of transition to the Little Ice Age [57]. Samples were taken from 6 females [48].

La Olmeda (Pedrosa de la Vega, Palencia)

At least 239 individuals have been recovered from this early Medieval cemetery (henceforth Olmeda) on the right bank of the Carrión River, occupied from the 7th to 13th centuries [58, 59]. Despite the importance of the osteological collection, only a few studies have been published, largely focused on the paleopathology of the skulls [60]. Samples were taken from 9 males and 10 females, mainly from the Medieval Climate Anomaly [5, 7, 61].

Sahl-ben-Malik cemetery (Cuesta del Hospicio sector, Granada)

Henceforth Granada cemetery, was the most important in the city of Granada during Medieval times [62]. It was occupied from the 11th to 15th century [63, 64], and most tombs date from the transition to or during the Little Ice Age [5, 6]. Samples were taken from 18 males and 12 females found under the present-day street called Cuesta del Hospicio. During Medieval times, Granada was supplied with water by the Darro and Genil Rivers and by the Aynadamar acequia from the Fuente Grande spring in nearby Alfacar [65, 66].

La Torrecilla (Arenas del Rey, Granada)

At least 152 individuals have been recovered in varied states of preservation from this cemetery (henceforth Torrecilla) of a small rural settlement on the Cacín River plain [67, 68]. According to radiocarbon dating values, most tombs are from the 13th to 15th centuries, i.e., the beginning of the Little Ice Age [6, 7]. Samples were taken from 11 males and 13 females [65, 69].

Talará cemetery (Valle de Lecrín, Granada)

Over 80 individuals have been recovered from this cemetery (henceforth Talará), which belonged to a farmhouse or rural settlement comparable to Torrecilla [68]. It lies below Sierra Nevada in the Lecrín valley on a natural route between the Mediterranean coast and the city of Granada. The tombs date from the 14th and 15th centuries [70], i.e., the beginning of the Little Ice Age [5, 7]. Samples were taken from 10 males and 10 females.

Mancoba (Baza, Granada)

Over 300 individuals have been recovered from this cemetery (henceforth Baza) in Baza, a city of special importance in the late Middle Ages due to its strategic location near the frontier with the Kingdom of Castile, its economic wealth, and its industrial production [71]. It was mainly supplied with water from the Guadiana Menor River [72]. According to radiocarbon dating, the cemetery was occupied in the 14th and 15th centuries. Samples were taken from 3 males and 4 females.

Samples

All samples studied (n = 145) were from upper first incisors unaffected by trauma, caries, or wear extracted from individuals aged over 20 years. The distal half of the crown analyzed corresponds to ages between 7 months and 4.5 years according to the atlas of AlQahtani et al., [73].

Analytical procedures

Carbon (δ13CenVPDB) and oxygen (δ18Oc VPDB) isotope values were determined in the structural carbonate of the enamel of the 145 incisors; analyses were conducted in the Stable Isotope Biogeochemistry Laboratory of the Instituto Andaluz de Ciencias de la Tierra (CSIC, Granada, Spain) using standard protocols [74, 75]. After scanning the teeth with an Artec Micro scanner and cleaning the dental surface to eliminate possible contaminants, the enamel was mechanically extracted with a microdrill and then pulverized. Next, ~10 mg of this powder was dissolved and processed, using chemical reagents to eliminate organic matter (1 mL 1.75% sodium hypochlorite for 45 min) and secondary carbonates (1 mL 0.1 M acetic acid for 15 min). Samples were subsequently lyophilized, treated with helium to eliminate atmospheric gases, and injected with 100% phosphoric acid at 72°C for ~ 2.5 h. Samples (burned to form CO2) were placed in a gas chromatographer (Finnigan Gas Bench II) and then in a Thermo Finnigan DELTA plus XP IRMS to measure isotope ratios, using two international standards (NBS18 and NBS19) and one internal standard (Cavendish Marble). All results were referred to the standard Vienna PeeDee Belemnite (VPDB) and expressed in delta (δ) notation as ‰: δ18O = ((18O/16O sample) / (18O/16O standard))– 1) * 1000 [8].

Statistical procedures

IBM SPSS 22 was used for statistical analyses. The Shapiro-Wilk test was applied to test distribution normality. The mean absolute deviation from the median multiplied by three (±3MADnorm) was used as a robust measure of scale for small sample sizes and non-normal distributions to detect outliers, considered appropriate for most biological data [14, 76]. We also considered ±2 standard deviations from the mean. The non-parametric Mann-Whitney test was performed to evaluate between-group and between-sex differences, setting statistical significance at 0.05.

Enamel δ18Oc (VPDB) values were transformed into phosphate (δ18OpVSMOW) and drinking water (δ18OdwVSMOW) values for comparisons with δ18Otsw (VSMOW) results for terrestrial surface water sources. The best procedure for this data transformation remains under debate [10, 30, 77], and we used three widely applied linear equations [7881, among others]:

δ18Oc (VSMOW) = (1.03091 * δ18Oc (VPDB)) + 30.91 [82]

δ18Op (VSMOW) = (1.122 * δ18Oc (VSMOW))– 9.6849 [10]

δ18Op (VSMOW) = (0.78 * δ18Odw (VSMOW)) + 22.70 [33]

δ18Oc (VSMOW) values were transformed into δ18Op (VSMOW) values by using a combination of Iacumin et al. [83] and Metcalfe et al. [84] linear equations for arid climates [10], which provide a satisfactory fit with the δ18Otsw (VSMOW) values from the study areas.

Results

S1 Table lists the δ13Cen (VPDB), δ18Oc (VPDB), and δ18Odw (VSMOW) values obtained for each sample and reports the sex of the individual. Table 2 exhibits mean δ13Cen, δ18Oc and δ18Odw values by site and sex. Fig 2 depicts δ13Cen and δ18Odw values by site and cultural group. Figs 3 and 4 depict the distribution of δ13Cen and δ18Odw values by sex and cultural group.

thumbnail
Fig 2. Individual δ13Cen (VPDB) and δ18Odw (VSMOW) values by site and cultural group.

https://doi.org/10.1371/journal.pone.0304313.g002

thumbnail
Fig 3. Box plot of δ13Cen (VPDB) values at sites by cultural group and sex.

https://doi.org/10.1371/journal.pone.0304313.g003

thumbnail
Fig 4. Box plot of δ18Odw (VSMOW) values at sites by cultural group and sex.

https://doi.org/10.1371/journal.pone.0304313.g004

thumbnail
Table 2. Mean δ13Cen, δ18Oc, and δ18Odw values by site for the whole sample and by sex.

https://doi.org/10.1371/journal.pone.0304313.t002

Regarding δ13Cen values, only one male at Tejuela (TE 26) and two females at Olmeda (OL 11 and OL 112) are outliers by ±3MADnorm, with one male at Torrecilla (TO 12) being very close to the ±3MADnorm cutoff. The same four individuals are outliers when ±2σ is applied (Fig 3). In relation to δ18Odw values, only one female at San Baudelio (SB 14) is an outlier by ±3MADnorm, although a female at Olmeda (OL 167) and a male at Torrecilla (TO 28) are outliers by ± 2σ, and a male at Torrecilla (TO 2) and a male at Talará (TA 19) are at the cutoff point (Fig 4).

The distribution of δ13Cen values did not differ among the four Christian sites in the Northern Peninsular or between the males and females at these sites, with the exception of a less negative mean value for females versus males at San Baudelio (p = 0.02). However, their distribution significantly differed (p<0.001) among the four Islamic sites in the South, with markedly less negative values at the rural (Torrecilla and Talará) versus urban (Granada and Baza) sites, while no significant between-sex difference was found at any site or between rural and urban sites. δ13Cen values significantly differed between the Christian and Islamic sites (p<0.001), observing a considerably less negative values in the latter.

Among the Christian sites, significantly lower mean δ18Oc and δ18Odw values (p<0.001) were recorded at San Baudelio than at the remaining sites except for Palacios, with no differences among the other sites. No between-sex difference in these values was observed at any site. Among Islamic sites, significantly lower mean δ18Oc and δ18Odw values (p<0.001) were observed at Baza and Talará than at Granada and Torrecilla, with no difference between Baza and Talará (p = 0.85) or between Granada and Torrecilla (p = 0.41). No between-sex difference in these values was observed at any site. Both δ18Oc and δ18Odw values were significantly lower (p<0.02) at the Christian sites in the North than at the Islamic sites in the South.

Discussion

Dietary patterns

The δ13Cen values suggest that the diet of the individuals from Tejuela incorporated a large portion of C3 plants, at least during their early childhood. However, the intake of some C4 type plants cannot be ruled out, especially common millet (Panicum miliaceum) and foxtail millet (Setaria italica), cultivated in the Iberian Peninsula since the Early Iron Age [85]. The diet of the outlier (TE 26) indicates a major consumption of C4 type plants. These data are not at odds with the average δ13C in bone collagen samples of -18.6 ± 0.6‰ (VPDB) previously calculated for the same cemetery [57], which pointed to a substantial dietary contribution of C3 plants while not excluding a possibly lesser consumption of C4 species. Similar values are encountered at San Baudelio, although the sexes significantly differed at this site, where the females showed a higher consumption of C4 plants. A similar difference was observed in δ13Ccol (bone collagen) values, which were a mean of -18.2±0.4‰ (VPDB) in the females [51], attributable to their distinct geographic origin. The δ13Cen values at Olmeda also reveal a mixed diet with a predominance of C3 plants but a higher consumption of C4 plants than at Tejuela or San Baudelio. The fact that these individuals lived during the Medieval Climate Anomaly may explain their greater intake of C4 plants, which are more characteristic of warmer environments, with the values simply corresponding to these types of climatic conditions [86]. The particularly high consumption of C4 plants by the two outlier females (OL 11, OL 112) at La Olmeda may indicate their early childhood in a different warmer location. Finally, δ13Cen values for the six females at Palacios suggest that they shared a C3-based diet with the possible occasional intake of C4 plants. The mean δ13Ccol (bone collagen) value of -19.4 ± 0.5‰ (VPDB) in Palacios [57] is consistent with the intake of C3 plants. Interestingly, the lowest mean values were found in the males at San Baudelio and females at Palacios (Table 3), which are at the highest altitudes and would therefore have experienced colder climates.

thumbnail
Table 3. Isotopic values of δ18Odw (VSMOW) in local water from different Spanish stations.

https://doi.org/10.1371/journal.pone.0304313.t003

Among the Islamic sites in the South of the Peninsula, the largest number of individuals are from the city of Granada. Their δ13Cen values are highly variable and indicate a mixed diet of both C3 and C4 plants, with a predominance of the former, as also observed in Baza, the other Islamic urban center studied. These results are consistent with the mean δ13C value of -17.1±1.2‰ (VPDB) previously reported in collagen from Granada [87], which also suggests a mixed diet with a major contribution of C3 plants. Clear differences were found between rural and urban Islamic sites. Samples from rural Torrecilla reveal a wide inter-individual variability, with an important intake of C4 plants that was very high in some individuals (e.g., TO 28). A lesser variability in values was observed at the other rural site, Talará, which showed an elevated consumption of C4 plants. Mean δ13C values in collagen are -16.0 ± 1.5‰ (VPDB) at Torrecilla and -15.3 ± 0.8‰ (VPDB) at Talará [69], in full agreement with the results obtained in enamel apatite. The similarity of results with the isotopic values from adult collagen in the studied collections suggests that, throughout the weaning process, the children received supplementary food incorporating the same or possibly similar plant resources as the rest of the community. The variation between the North and South of the Peninsula can be attributed to differences in climate [88, 89] and diet.

When the Arabs arrived in the Iberian Peninsula (8th century), they engaged in a complex process of introduction, reimplantation, and diffusion of certain plants, some of which were acclimatized in the botanic gardens of the royal courts [3]. Citruses, rice, and the C4 plants sugarcane and sorghum subsequently reached kingdoms in the North of the Peninsula [90]. Sugarcane is solely a carbohydrate and contains no amino acids, hampering its detection by isotopic analysis, although ~3% of natural sugarcane juice and molasses is protein [91, 92], which would enrich its δ13Cen value. Sugar was used in pharmacy and cooking but was always a luxury item reserved for special occasions, mainly among the wealthier classes [93, 94]. However, its consumption increased in the 14th-15th century during Nasrid times, and the only site of sugarcane cultivation during the late Middle Ages was on the Mediterranean coast of Granada province [95]. Indeed, the 14th century Granada writer Ibn al-Jatib recommended the use of sugarcane and crystalized sugar to calm children during weaning (in the second year of life) [93], and the individuals in this study may therefore have consumed sugar during their childhood [96], although it is not possible in our study to further precise the age of weaning process.

The other C4 type vegetable, sorghum, must have adapted very well to conditions in Granada, whose climate and altitude do not favor the cultivation of wheat, the cereal in greatest demand [97]. Wheat was mainly imported from North Africa and reserved for wealthier families [90, 94, 98]. Ibn-al Jatib and other contemporary writers such as Abū l-Jayr and Ibn Razin al-Tuŷībī underscored the nutritional value of wheat, describing sorghum as a cereal consumed by less favored social classes and rural populations and in times of shortage [90, 94, 98]. This would explain the greater consumption of sorghum at rural sites such as Torrecilla and Talará, while social differences would account for the variability of isotopic values in urban areas.

Environment

Although our complete dataset features 145 individuals, the study is limited by the very small sample size for some sites (e.g., Palacios or Baza), where it was not possible to detect any significant between-sex differences. In addition, the conversion of 18Oc (VPDB) to δ18Odw (VSMOW) is affected by a high predictive error [10, 14, 30, 77, 99], which is why Table 2 displays both values for each individual. Furthermore, the comparisons are based on isotopic oxygen data for water that does not always derive from the precise location of the site. The characteristics of current water may vary from those during the investigated period, and there may be differences between the origin of the water (rainfall or rivers) and the water consumed at the site.

Among the sites in the Northern Peninsular, the highest mean δ18Oc and δ18Odw values were observed at Tejuela, likely because it has lowest altitude above sea level (Table 1) and was occupied during the Medieval Climate Anomaly. Similar values are recorded at the site of La Olmeda, which is at a greater height above sea level and has a drier climate but was also occupied during the Medieval Climate Anomaly [5, 6]. No between-sex differences in these values were observed at either site. The lowest mean δ18Oc and δ18Odw values were found at San Baudelio and were similar to those observed at Palacios, with both sites being located at the highest altitudes (Table 1). A much lower value is shown by one female (SB 14) at San Baudelio. Both San Baudelio and Palacios were occupied during the phase of transition to the Little Ice Age [6, 7]. In the present day, all four sites have similar climate, with mild summers, although Tejuela and San Baudelio are wetter (Table 1). There are also no differences in current rainwater δ18Odw values among these areas (Table 3), all in a similar geographic environment on the North sub-plateau, a large sedimentary basin surrounded by high mountain ranges where relatively flat lands are crossed by fluvial valleys, with a mean height of 750 m a.s.l., mild and dry summers, and cold winters [100]. Hence, differences among the Northern sites may be attributable to distinct climatic conditions at the time of their occupation rather than to climate differences within the region.

Differences in mean values between the Christian sites in the North of the Iberian Peninsula and the Islamic sites in the South can be explained by their distinct ecosystems [88, 89]. The area of Granada is characterized by a richness and variety of biotopes favored by the presence of the mountain range of Sierra Nevada, which acts as a geological and geographic barrier, by its proximity to the sea, and by the presence of meadows and high plateaus [107]. This would account for different climatic conditions in Baza (Table 1) and the highly varied rainwater δ18Odw values in the present day. Mean findings in Granada and Torrecilla are similar to current values in Granada city and Linares (Jaen). Baza is currently the coldest site, with a mean minimum temperature in January of -0° C [108], which may explain the more negative mean oxygen finding. However, a similar mean value was recorded at Talará, although the climate at this site is the same as that of Granada and Torrecilla. This discrepancy may result from its localization in the Valley of Lecrín at the foot of Sierra Nevada, given that water supplied by rivers from the mountains or by springs fed by melted ice would have lower oxygen isotopic values [109]. In this way, rainwater oxygen values from the nearby village of Bérchules, also at the foot of Sierra Nevada, are lower than those of Granada and Linares and similar to those in Baza (Table 3). Besides the geographic and climatic differences among these sites, both Granada and Torrecilla included individuals that lived in the phase of transition to the Little Ice Age and all individuals at Baza and Talará lived during this period [6, 7].

Mobility

Some individuals are outliers by both ±3MADnorm and ± 2 standard deviations from the mean, indicating a possible non-local origin. We highlight the δ18Odw of the female (SB 14) at San Baudelio, where a previous study [51] found that the carbon ratios in bone collagen significantly differed between females and males, suggesting the distinct origin of the former. No female at this site had reached the age of 30 years, and the authors proposed that the results would be attributable to the diet consumed before they left their place of origin to marry elsewhere. San Baudelio was a small farm that only had space for around two or three families [50], and it would have been necessary to bring in females to avoid consanguinity. This proposal is supported by the present δ13Cen data, which indicate that the diet of the males and females differed during their first years of life. In fact, carbon isotope values were higher in the females than in the males, which may suggest that they came from a warmer environment. On the other hand, the similar oxygen isotope values between the females and males suggest that their place of origin would not have been very distant and may have had a similar climate but at a lower altitude, although the much lower oxygen isotope value in the female outlier (SB 14) indicates an origin in a much colder climate. Two females at La Olmeda (OL11 and OL112) are outliers by δ13Cen and another (OL 167) is an outlier by δ18Odw, and they likely came from a warmer place, especially OL 167. This may suggest an exogamic pairing, a common practice in Medieval Castile [110]. However, although C4 plants are more common in warmer environments, supporting this proposition, the results for OL11 and OL112 may also have a socioeconomic explanation, with the consumption of less valued C4 plants [97] pointing to a lower social class, in line with other medieval findings in the Iberian Peninsula [42]. Among males, the diet of one adult male (TE 26) during childhood markedly differed from that of other individuals at Tejuela, whose demography indicates the recent foundation of this village [111]. This result again raises the possibility that his early childhood was spent in a warmer environment but may also reflect a lower social status. Among the Islamic sites in the South of the Peninsula, two males (TO 2 and TA 19) appear to have spent their childhood in a colder environment and may possibly have moved to the last Islamic territory remaining after the southward advance of the Christian Monarchs, i.e., the Nasrid Kingdom of Granada [112]. In contrast, one male at Torrecilla (TO 28) appears to have come from a much warmer place and may possibly have spent his childhood in Northern Africa, with this type of migration being documented in historical sources [113]. It is worth mentioning that the breastfeeding period and the weaning process may have played some influence on the oxygen isotopic ratios of the analyzed individuals [15]. Body water, and therefore breast milk, features higher δ18O values than drinking water [114]. When considering data from different teeth featuring different forming periods, this leads to a descending curve in the diachronic trajectory of oxygen isotopic ratios (from enriched to the level of the local drinking water [115117]. It is clear that these patterns, if not taken into account, may mimic (or mask) isotopic differences related to environmental variables. In our case, this potential bias cannot be clarified due to the applied analytical approach but it needs to be taken into account.

Conclusions

This study provides insights into dietary differences between Medieval populations from the Christian North and Islamic South of the Iberian Peninsula. There was a greater intake of C4 plants by the Muslims, likely attributable to their introduction of sugarcane and sorghum. This cereal is typical of warm climates, and its quality is considered inferior to that of wheat. C4 plant consumption was also higher in rural versus urban Islamic sites. Oxygen isotope values from enamel apatite differ between populations in the North and South of the Peninsula, consistent with the differences in their climates. Isotopic variability within each region can be attributed to diachronic occupation phases under varying climatic conditions. The analyses identified a few individuals who were possibly nonlocal, including females who may have arrived from elsewhere for the purpose of marriage.

Supporting information

S1 Table. Individual δ13Cen, δ18Oc, and δ18Odw values.

TE: Tejuela; SBB: San Baudelio; OL: La Olmeda; PA: Palacios; GR: Granada; TO: La Torrecilla; TA: Talará; BA: Baza. UI1: first upper incisor.

https://doi.org/10.1371/journal.pone.0304313.s001

(DOCX)

Acknowledgments

This research forms part of the PhD thesis of JFMA.

References

  1. 1. Carvajal López JC, editor. Al-Andalus: archaeology, history and memory. UCL Qatar series in archaeology and cultural heritage, vol 3. Edinburgh: Akkadia Press; 2016.
  2. 2. Collins R, Goodman A, editors. Medieval Spain: Culture, Conflict and Coexistence. New York: Palgrave MacMillan; 2002.
  3. 3. García Sánchez E. Caña de azúcar y cultivos asociados en al-Andalus. In: Malpica A, editor. Paisajes del azúcar. Granada: Diputación Provincial; 1995.p. 41–68.
  4. 4. Martín Civantos JM. Intensive irrigated agriculture in al-Andalus. In: Carvajal López JC, editor. Al-Andalus: archaeology, history and memory. UCL Qatar series in archaeology and cultural heritage, vol 3. Edinburgh: Akkadia Press; 2016. p. 27–31
  5. 5. Corella JP, Stefanova V, El Anjoumi A, Rico E, Giralt S, Moreno A, et al. A 2500-year multi-proxy reconstruction of climate change and human activities in northern Spain: the Lake Arreo record. Palaeogeogr Palaeoclimatol, Palaeoecol. 2013; 386:555–568.
  6. 6. Moreno Moreno A, Perez A, Frigola J, Nieto-Moreno V, Rodrigo-Gámiz M, Martrat B, et al. The Medieval climate anomaly in the Iberian Peninsula reconstructed from marine and lake records. Quat Sci Rev. 2012; 43: 16–32.
  7. 7. Sánchez-López G, Hernández A, Pla-Rabés S, Trigo RM, Toro M, Granados I, et al. Climate reconstruction for the last two millennia in central Iberia: The role of East Atlantic (EA), North Atlantic Oscillation (NAO) and their interplay over the Iberian Peninsula. Quat Sci Rev. 2016; 149: 135–150.
  8. 8. Fry B. Stable isotope ecology. New York: Springer; 2006.
  9. 9. Hedges REM, Clement JG, Thomas CDL, O’Connell TC. Collagen turnover in the adult femoral mid-shaft: modelled from anthropogenic radiocarbon tracer measurements. Am J Phys Anthropol. 2007; 133: 808–816.
  10. 10. Chenery CA, Pashley V, Lamb AL, Sloane HJ, Evans JA. The oxygen isotope relationship between the phosphate and structural carbonate fractions of human bioapatite. Rapid Commun Mass Spectrom. 2012; 26: 309–319. pmid:22223318
  11. 11. Kendall C, Erikson AM, Kontopoulos I, Collins MJ, Tuner-Walker G. Diagenesis of archaeological bone and tooth. Palaeogeogr Palaeoclimatol Palaeoecol. 2018; 491: 21–37.
  12. 12. Koch PL, Tuross N, Fogel ML. The effects of sample treatment and diagenesis on the isotopic integrity of carbonate in biogenic hydroxylapatite. J Archaeol Sci.1997; 24: 417–429.
  13. 13. Sponheimer M, Lee-Thorp J. Oxygen isotopes in enamel carbonate and their ecological significance. J Archaeol Sci. 1999; 26 (6): 723–728.
  14. 14. Lightfoot E, O’Connell T. On the Use of Biomineral Oxygen Isotope Data to Identify Human Migrants in the Archaeological Record: Intra-Sample Variation, Statistical Methods and Geographical Considerations. PLoS One. 2016; 11 (4), e0153850. pmid:27124001
  15. 15. Chinique de Armas Y, Mavridou AM, Domínguez JG, Hanson K, Laffoon J. Tracking breastfeeding and weaning practices in ancient populations by combining carbon, nitrogen and oxygen stable isotopes from multiple non-adult tissues. PLoS One. 17(2), e0262435, pmid:35108296
  16. 16. Ambrose SH, Norr L. Experimental evidence for the relationship of the carbon isotope ratios of whole diet and dietary protein to those of bone collagen and carbonate. In: Lambert JB, Grupe G, editors. Prehistoric human bone-archaeology at the molecular level. Berlin: Springer-Verlag; 1993. p. 1–37.
  17. 17. Krueger HW, Sullivan CH. Models for carbon isotope fractionation between diet and bone. ACS Symp Ser. 1984; 258:205–220
  18. 18. Tieszen LL, Fagre T. Effect of diet quality and composition on the isotopic composition of respiratory CO2, bone collagen, bioapatite and soft tissues. In: Lambert JB, Grupe G, editors. Prehistoric human bone: archaeology at the molecular level. Berlin: Springer-Verlag; 1993. p.121–155.
  19. 19. Díaz del Río P, Waterman A, Thomas J, Peate D, Tycot R, Martínez-Navarretre MI, et al. Diet and mobility patterns in the Late Prehistory of central Iberia (4000–1400 cal BC): the evidence or radiogenic (87Sr/86Sr) and stable δ18O, δ13C) isotope ratios. Archaeol Anthropol Sci. 2017; 9:1439–1452.
  20. 20. Kohn MJ, Cerling TE. Stable isotope compositions of biological apatite. Rev Miner Geochem. 2002; 48(1):455–488.
  21. 21. Lai L. The interplay of economic, climatic and cultural change investigated through isotopic analyses of bone tissue: the case of Sardinia 4000–1900 B.C. Dissertation, University of South Florida; 2008.
  22. 22. Tykot RH, Falabella F, Planella MT, Aspillaga E, Sanhueza L, Becker C. Stable isotopes and archaeology in central Chile: methodological insights and interpretative problems for dietary reconstruction. Int J Osteoarchaeol. 2009; 19(2):156–170.
  23. 23. Rebollar JLG, Sancho AC, editors. C4 y CAM. Características generales y uso en programas de desarrollo de tierras áridas y semiáridas. Homenaje del doctor Julio López Gorgé. Madrid: Editorial CSIC-CSIC Press; 2010.
  24. 24. Guede I, Ortega LA, Zuluaga MC, Alonso-Olazabal A, Murelaga X, Pina M, et al. Isotope analyses to explore diet and mobility in a medieval Muslim population at Tauste (NE Spain). PLoS One. 2017;12(5), e0176572. pmid:28472159
  25. 25. Guede I, Zuluaga MC, Ortega LA, Alonso-Olazábal A, Murelaga X, García Camino I, et al. Social structuration in medieval rural society based on stable isotope analysis of dietary habits and mobility patterns: San Juan de Momoitio (Biscay, North Iberian Peninsula). J Archaeol Sci Rep. 2020; 31.
  26. 26. Serna A, Prates L, Valenzuela LO, Salazar-García DC. Back to the bases: Building a terrestrial water δ18O baseline for archaeological studies in North Patagonia (Argentina). Quat Int. 2019; 548: 4–12.
  27. 27. Bryant J, Froelich P. A model of oxygen isotope fractionation in body water of large mammals. Geochim Cosmochim Acta. 1995; 59 (21): 4523–4537.
  28. 28. Kohn M. Predicting animal δ18O: Accounting for diet and physiological adaptation. Geochim Cosmochim Acta.1996; 60: 4811–4829
  29. 29. O’Grady S, Valenzuela LO, Remien C, Enright E, Jorgensen M, Kaplan I, et al. Hydrogen and oxygen isotope ratios in body water and hair: Modeling isotope dynamics in nonhuman primates. Am J Primatol.2012; 74 (7): 651–660. pmid:22553163
  30. 30. Daux V, Lécuyer C, Héran M, Amiot R, Simon L, Fourel F, et al. Oxygen isotope fractionation between human phosphate and water revisited. J Hum Evol. 2008; 55 (6):1138–1147. pmid:18721999
  31. 31. Podlesak D, Torregrossa A, Ehleringer J, Dearing M, Passey B, Cerling T. Turnover of oxygen and hydrogen isotopes in the body water, CO2, hair, and enamel of a small mammal. Geochim Cosmochim Acta. 2008; 72 (1): 19–35.
  32. 32. Longinelli A. Oxygen isotopes in mammal bone phosphate: a new tool for paleohydrological and paleoclimatological research? Geochim Cosmochim Acta. 1984; 48 (2): 385–390.
  33. 33. Luz B, Kolodny Y, Horowitz M. Fractionation of oxygen isotopes between mammalian bone-phosphate and environmental drinking water. Geochim Cosmochim Acta.1984; 48 (8): 1689–1693.
  34. 34. Darling WG. Hydrological factors in the interpretation of stable isotopic proxy data present and past: A European perspective. Quat Sci Rev. 2004; 23(7–8):743–770.
  35. 35. Kendall C, Coplen T. Distribution of oxygen-18 and deuterium in river waters across the United States. Hydrol Process. 2001; 15: 1363–1393.
  36. 36. Darling WG, Bath AH, Gibson JJ, Rozanski K. Isotopes in water. In: Leng MJ, editor. Isotopes in paleoenvironmental research. London: Springer: 2006. p.1–52.
  37. 37. Rozanski K, Araguas-Araguas L, Gonfiantini R. Isotopic patterns in modern global precipitation. Geophys Monog. 1993; 78: 1–36.
  38. 38. Dury G, Lythe A, Márquez-Grant N, García-Rubio A, Graziani G, Mari J, et al. The Islamic cemetery at 33 Bartomeu Vicent Ramon, Ibiza: investigating diet and mobility through light stable isotopes in bone collagen and tooth enamel. Archaeol Anthropol Sci. 2019; 11:3913–3930.
  39. 39. Inskip S, Carroll G, Waters-Rist A, López-Costas O. Diet and food strategies in a southern al-Andalusian urban environment during Caliphal period, Écija, Sevilla. Archaeol Anthropol Sci. 2019; 11: 3857–3874.
  40. 40. Pérez-Ramallo P, Grandal-d’Anglade A, Organista E, Santos E, Chivall D, Rodríguez-Varela R, et al. Multi-isotopic study of the earliest mediaeval inhabitants of Santiago de Compostela (Galicia, Spain). Archaeol Anthtropol Sci. 2022;14. 214.
  41. 41. Prevedorou E, Díaz-Zorita M, Romero A, Buikstra J, de Miguel MP, Knudson K. Residential mobility and dental decoration in Early Medieval Spain: Results from eight century site of Plaza del Castillo, Pamplona. Dent Anthropol. 2010; 23: 42–52.
  42. 42. Alexander MM, Gerrard CM, Gutierrez A, Millard AR. (2015). Diet, society, and economy in late medieval Spain: stable isotope evidence from Muslims and Christians from Gandia, Valencia. Am J Phys Anthropol. 2015; 156: 263–273. pmid:25351146
  43. 43. Lubritto C, García-Collado MI, Ricci P, Altieri S, Sirignano C, Quirós Castillo JA. New dietary evidence on Medieval Rural Communities of the Basque Country (Spain) and its Surroundings from Carbon and Nitrogen Stable Isotope Analyses: Social Insights, Diachronic Changes and Geographic Comparison, Int J Osteoarchaeol, 2017; 27: 984–1002.
  44. 44. Peel MC, Finlayson BL, McMahon TA. Updated world map of the Köppen-Geiger climate classification. Hydrol Earth Syst Sci. 2007; 11: 1633–1644.
  45. 45. Castillo Yurrita A del. Excavaciones altomedievales en las provincias de Soria, Logroño y Burgos. Madrid: Ministerio de Educación y Ciencia; 1972.
  46. 46. Palomino Lázaro AL, Negredo García M, editors. La comunidad aldeana de Tejuela en época medieval. Arqueología funeraria y doméstica en el Alto Valle del Ebro. Burgos: Diputación de Burgos; 2023.
  47. 47. Martín-Alonso JF, Maroto Benavides RM, Jiménez-Brobeil SA. Esqueletos inhumados en cementerios excavados en roca: el caso de Tejuela/Villanueva de Soportilla (Burgos). AESPA. 2021; 94.
  48. 48. Maroto RM. Antropología de las poblaciones femeninas medievales del Alto Ebro y Alto Duero. Phd thesis. Granada: Universidad de Granada; 2004. Available from: https://digibug.ugr.es/handle/10481/1840
  49. 49. Andrío J, Loyola E. Necrópolis medieval de San Baudelio de Berlanga. Temas Sorianos. 1992; 20:1071–1086.
  50. 50. Ph Banks, Zozaya J, Larren H, Ceretti Z, Bate M. Excavaciones en San Baudelio de Casillas de Berlanga (Soria). Noticiario Arqueológico Hispánico. 1983; 16: 381–440.
  51. 51. Jiménez-Brobeil SA, Maroto RM, Laffranchi Z, Roca MG, Granados Torres A, Delgado Huertas A. Exploring diet in an isolated medieval rural community of Northern Iberia: The case study of San Baudelio de Berlanga (Soria, Spain). J Archaeol Sci Rep. 2020; 30.
  52. 52. Souich Ph du, Botella MC, Ruiz L. Antropología de la población medieval de Palacios de la Sierra (Burgos). Boletín de la Sociedad Española de Antropología Biológica.1990;11:117–146.
  53. 53. Carmona Ballestero E. Releyendo las estelas epigráficas de la necrópolis de “El Castillo” (Palacios de la Sierra, Burgos). Arqueología y Territorio Medieval. 2019; 26: 137–154.
  54. 54. Álvaro Rueda K, Travé Allepuz E, López Pérez MD. Excavaciones arqueológicas en el yacimiento altomedieval de Revenga: nuevos datos para el conocimiento de los espacios de hábitat altomedieval en el alto Arlanza (Burgos). Territorio, Sociedad y Poder. 2018;13: 5–21.
  55. 55. De la Cruz V. Notas para la historia de Palacios de la Sierra. Boletín de la Institución Fernán González. 1968; 171: 305–311.
  56. 56. López Pérez MD, Álvaro Rueda K, Travé Allepuz E. Rock-cut cemeteries and settlements processes at the Upper Arlanza Basin (Burgos, Spain): a Late Antique and Early Medieval landscape analysis. Zephyrus. 2016; LXXVIII: 173–191.
  57. 57. Martín-Alonso JF, Maroto RM, Roca MG, López O, Montalvo S, Jiménez-Brobeil SA. Diferentes modos de vida, diferentes dietas. Caries e isótopos estables en dos poblaciones burgalesas medievales. Munibe. 2022; 73: 191–204.
  58. 58. Turbón D, Hernández M. La necrópolis medieval de La Olmeda. Memoria de excavación. 1982. Avalaible from: http://fonspalol.icac.cat/041.004.000.pdf
  59. 59. Vigil-Escalera Guirado A. Apuntes sobre la genealogía política de aldeas y granjas altomedievales. In: Martín Viso I, editor. ¿Tiempos Oscuros? Territorios y Sociedad en el Centro de la Península Ibérica (siglos VII–X) (I. ed.). Madrid: Sílex;2009. p. 31–44.
  60. 60. Campillo D, Turbón D, Hernández M. Estudio paleopatológico preliminar de la necrópolis medieval de La Olmeda (Pedrosa de la Vega, Palencia). VIII Congreso Nacional de Historia de la Medicina. Murcia-Cartagena. 1986. Avalaible from: https://fonspalol.icac.cat/042.002.020.pdf
  61. 61. Hernández M, Turbón D. Parámetros del esqueleto postcraneal en la población medieval castellana de “La Olmeda”. Bol Soc Esp Antrop Biol. 1991;12:61–80.
  62. 62. López López M. Gestos funerarios y rituales. La necrópolis musulmana de la Puerta de Elvira (Granada). Granada: Universidad de Granada; 1997.
  63. 63. Espinar Moreno M. La necrópolis de Sahl o Saad Ben Malik de Granada a través de algunas intervenciones arqueológicas. In: Espinar M, editor. La muerte desde la Prehistoria a la Edad Moderna. Granada: Libros EPCCM; 2018.p. 455–480.
  64. 64. Sarr B. al-Andalus Del Magreb a. Los ziríes y la fundación de Madīnat Garnāta. In: Sarr B, editor. Tawa’if. Historia y Arqueología de los Reinos de Taifas. Granada: Alhulia; 2018. p.563–598.
  65. 65. Charisi D, Laffranchi Z, Jiménez-Brobeil SA. Sexual dimorphism in two mediaeval Muslim populations from Spain. Homo. 2016; 67: 397–408. pmid:27659541
  66. 66. Jiménez-Brobeil SA, Martín-Alonso JF, Charisi D, López-Gijón R, Maroto RM. Aproximación a los modos de vida en la Granada medieval a partir de la patología dental. Revista del CEHGR. 2023; 35:59–76.
  67. 67. Arribas A, Riu M. La necrópolis y poblado de La Torrecilla (Pantano de los Bermejales, provincia de Granada). Anuario de Estudios Medievales. 1974; 9: 17–40.
  68. 68. Trillo-San José C. Agua, tierra y hombres en Al-Andalus. La dimensión agrícola del mundo nazarí. Granada: Ajbar; 2004.
  69. 69. Jiménez-Brobeil SA, Charisi D, Laffranchi Z, Maroto RM, Delgado Huertas A, Milella M. Sex differences in diet and life conditions in a rural Medieval Islamic population from Spain (La Torrecilla, Granada): an isotopic and osteological approach to gender differentiation in al-Andalus. Am J Phys Anthropol. 2021; 175: 794–815. pmid:33772756
  70. 70. Espinar Moreno M. Hábices de la Mezquita Aljama de Madina Garnata o Iglesia Mayor de Granada en el Valle de Lecrín. Studia Orientalia. 2009;107: 51–80.
  71. 71. Sarr B. ¨Lo que quiero de estas tierras es Baza”. La evolución histórica de la Baza andalusí a través de las fuentes árabes. Péndulo. Papeles de Bastitania. 2015; 16:37–54.
  72. 72. Malpica A. Territorio y poblamiento en la frontera nororiental granadina. La Hoya de Baza y el Altiplano. Anales de la Universidad de Alicante. Historia medieval. 2017/2018; 20: 211–237.
  73. 73. AlQahtani SJ, Hector MP, Liversidge HM. Brief communication: The London Atlas of Human Tooth Development and Eruption. Am J Phys Anthropol. 2010; 142:481–490. pmid:20310064
  74. 74. Lee-Thorp J, Manning L, Sponheimer M. Problems and prospects for carbon isotope analysis of very small samples of fossil tooth enamel. Bull Soc Geol Fr. 1997;168: 767–773.
  75. 75. Stowe MJ, Sealy J. Terminal Pleistocene and Holocene dynamics of southern Africa’s winter rainfall zone based on carbon and oxygen isotope analysis of bovid tooth enamel from Elands Bay Cave. Quat Int. 2015; 404: 57–67.
  76. 76. Leys C, Ley C, Klein O, Bernard P, Licata L. Detecting outliers: Do not use standard deviation around the mean, use absolute deviation around the median. J Exp Soc Psychol. 2013; 49 (4): 764–766.
  77. 77. Pollard AM, Pellegrini M, Lee-Thorp JA. Technical note: Some observations on the conversion of dental enamel δ18op values to δ18ow to determine human mobility. Am J Phys Anthropol. 2011; 145: 499–504. pmid:21541927
  78. 78. Barberena R, Durán VA, Novellino P, Winocur D, Benítez A, Tessone A, et al. Scale of human mobility in the southern Andes (Argentina and Chile): A new framework based on strontium isotopes. Am J Phys Anthropol. 2017; 164: 305– 320. pmid:28631376
  79. 79. Buzon M, Conlee C, Bowen G, 2011. Refining oxygen isotope analysis in the Nasca region of Peru: an investigation of water sources and archaeological samples. Int J Osteoarchaeol. 2011; 21 (4): 446–455.
  80. 80. Knudson KJ. Oxygen isotope analysis in a land of environmental extremes: The complexities of isotopic work in the Andes. Int J Osteoarchaeol. 2009;19 (2): 171–191.
  81. 81. Lightfoot E, Šlaus M, O’Connell TC. Water consumption in Iron Age, Roman, and early medieval Croatia. Am J Phys Anthropol. 2014; 154 (4): 535–543. pmid:24888560
  82. 82. Coplen T, Kendall C, Hopple J. Comparison of stable isotope reference samples. Nature. 1983; 302(5905), 236.
  83. 83. Iacumin P, Bocherens H, Mariotti A, Longinelli A. 1996. Oxygen isotope analyses of coexisting carbonate and phosphate in biogenic apatite: A way to monitor diagenetic alteration of bone phosphate? Earth Planet Sci Lett. 1996;142: 1–6.
  84. 84. Metcalfe JZ, Longstaffe FJ, White CD. Method-dependent variations in stable isotope results for structural carbonate in bone bioapatite. J Archaeol Sci. 2009; 36 (1): 110–121.
  85. 85. Buxó R. Arqueología de las plantas. La explotación económica de las semillas y los frutos en el marco mediterráneo de la Península Ibérica. Barcelona: Crítica; 1997.
  86. 86. Goude G, Fontugne M. Carbon and nitrogen isotopic variability in bone collagen during the Neolithic period: influence of environmental factors and diet. J Archaeol Sci. 2016; 70:117–131.
  87. 87. Jiménez-Brobeil S, Martín-Alonso JF, Charisi D, Maroto RM. Avance al estudio de la paleodieta en la ciudad de Granada en época medieval. Cuadernos de la Alhambra. on press.
  88. 88. Machado MJ, Benito G, Barrientos M, Rodrigo FS. 500 years of rainfall variability and extreme hydrological events in southeastern Spain drylands. J Arid Env. 2011; 75: 1244–1253.
  89. 89. Martín-Puertas C, Valero-Garcés BL, Mata P, González-Sampériz P, Bao R, Moreno A. Arid and humid phases in Southern Spain during the last 4000 years: the Zóñar lake record, Córdoba. Holocene. 2008;18: 907–021.
  90. 90. Hernández Bermejo JE, García Sánchez E. Economic botany and ethnobotany in al-Andalus (Iberian península: tenth-fifteenth centuries). An unknown heritage of Mankind. Econ Bot. 1998; 52: 15–26.
  91. 91. Aguilar J, Espinoza M, Cabanillas J, Ávila I, García A, Julca J, et al. Evaluación de la cinética de crecimiento de saccharomyces cerevisiae utilizando un medio de cultivo a base de melaza de caña y suero lácteo. Agroind Sci. 2015; 5(1): 37–47.
  92. 92. Larrahondo JE. Composición química de la caña y factores que afectan la determinación de sacarosa y el proceso azucarero. XIV Congreso de técnicas azucareras de Guatemala. Available from: www.atagua.org/presentaciones/XIVCongresoNacional2017/fabrica/composicion_quimica_dr_larrahondo.pdf
  93. 93. García Sánchez E. El azúcar en la alimentación de los andalusíes. In: Malpica A, editor. La caña de azúcar en tiempos de los grandes descubrimientos (1450–1550). Granada: Diputación Provincial-Universidad de Granada; 1990.p. 209–231.
  94. 94. García Sánchez E. La alimentación popular urbana en al-Andalus. Arqueología Medieval. 1996; 4: 219–235.
  95. 95. Malpica Cuello A. La vida agrícola y la ganadería en al-Andalus y en el reino nazarí de Granada. In: Marín R, editor. Homenaje al profesor Dr. D. José Ignacio Fernández de Viana y Vieites. Granada: Universidad de Granada; 2012.p.213–228.
  96. 96. Jiménez-Brobeil SA, Maroto RM, Milella M, Laffranchi Z, Reyes Botella C. Introduction of sugarcane in Al-Andalus (Medieval Spain) and its impact on children’s dental health. Int J Osteoarchaeol. 2022;32: 283–293.
  97. 97. Peña-Chocarro L, Pérez-Jordá G, Alonso N, Antolín F, Teira-Brión A, Tereso JP, et al. Roman and medieval crops in the Iberian Peninsula: a first overview of seeds and fruits from archaeological sites. Quat Int. 2019; 499: 49–66
  98. 98. García Sánchez E. La alimentación en la Andalucía Islámica. Estudio histórico y bromatológico I. Andalucía Islámica. Textos y Estudios. 1981–82; II-III: 139–176.
  99. 99. Iacumin P, Venturelli G. The δ18O of phosphate of ancient human biogenic apatite can really be used for quantitative palaeoclimatic reconstruction? Eur Sci J. 2015; 11(9): 221–235. %.
  100. 100. Sánchez Zurro D. Geografía de Castilla y León. Valladolid: Ámbito; 2008.
  101. 101. IAEA/WMO (2015). Global Network of Isotopes in Precipitation. The GNIP Database. Available from: https://www.iaea.org/services/networks/gnip
  102. 102. Soto Castro H. Elaboración de mapas de contenidos isotópicos de O-18 en la precipitación sobre la Península Ibérica por medio de técnicas geoestadísticas. Tfm. Valencia: Universidad Politécnica de Valencia; 2017. Available from: https://m.riunet.upv.es/handle/10251/80278?show=full
  103. 103. Delgado Huertas A, Núñez R, Caballero E, Jiménez Cisneros C, Reyes E. Composición isotópica del agua de lluvia en Granada. IV Congreso Geoquímica de España. Monografía. Soria: CEDEX; 1992. p.350-358.
  104. 104. Bowen G, Ehleringer J, Chesson L. European water sample H and O isotope ratios, HydroShare. 2017.
  105. 105. Benavente Herrera J, Hidalgo Estévez MC, Izquierdo del Arco A, El Mabrouki K, Rubio Campos JC. Contenido en cloruros y en isótopos estables (18O y D) de las precipitaciones en un área montañosa (Alto Guadalquivir, provincia de Jaén. Geogaceta. 2004; 36: 111–114.
  106. 106. Molina Rojas AM, González Ramón A, Barberá JA, Peregrina del Río M, A. Beatriz Villagómez Antequera AB, Díaz Puga MA, et al. Caracterización físico-química e isotópica del agua subterránea relacionada con acequias de careo. Cuenca del río Bérchules (Sierra Nevada, Sur de España). Geogaceta. 2022; 71: 39–42. https://recyt.fecyt.es/index.php/geogaceta
  107. 107. Jabaloy A, Galindo-Zaldívar J, Sanz de Galdeano C. Guía geológica: Granada. Guía de la naturaleza. Granada: Diputación de Granada; 2008.
  108. 108. https://es.weatherspark.com/y/38280/Clima-promedio-en-Baza-Espa%C3%B1a-durante-todo-el-a%C3%B1o
  109. 109. Martín Chivelet J, Muñoz-García MB. Estratigrafía de isótopos de oxígeno y la reconstrucción de los cambios climáticos en el pasado. Enseñanza de las Ciencias de la Tierra. 2015; 23: 160–170.
  110. 110. Lisón Tolosana C. Estructura antropológica de la familia en España. In: Rof Carballo J, editor. La familia, diálogo recuperable. Madrid: Karpos; 1976. p. 37–51.
  111. 111. Jiménez-Brobeil SA, Maroto Benavides RM, Roca MG, Martín-Alonso JF. La población altomedieval de Sta. María de Tejuela (Bozoó, Burgos). Notas paleodemográficas, Munibe. 2020; 71: 181–191.
  112. 112. Solórzano F, Martín Pérez F, editors. Rutas de comunicación marítima y terrestre en los Reinos Hispánicos durante la Baja Edad Media. Movilidad, conectividad y gobernanza. Madrid: Ediciones de la Ergástula; 2020.
  113. 113. Villaverde Moreno J. Aportaciones de los emigrantes magrebíes al Reino nazarí de Granada entre los siglos XII y XIV. In: Ruiz Álvarez R, Moral Montero E, editors. Gentes que vienen y van. Estudios en torno a las migraciones: ayer, hoy y mañana. Granada: Universidad de Granada; 2020. p. 25–41.
  114. 114. Lin GP, Rau YH, Chen YF, Chou CC, Fu WG. Measurements of δD and δ18O Stable Isotope Ratios in Milk. J Food Sci. 2003; 68: 2192–2195.
  115. 115. Wright LE, Schwarcz HP. Stable carbon and oxygen isotopes in human tooth enamel: identifying breastfeeding and weaning in prehistory. Am J Phys Anthropol. 1998;106(1):1–8. pmid:9590521
  116. 116. Tsutaya T, Yoneda M. Reconstruction of breastfeeding and weaning practices using stable isotope and trace element analyses: A review. Am J Phys Anthropol. 2015; 156: 2–21. pmid:25407359
  117. 117. Pederzani S, Britton K. Oxygen isotopes in bioarchaeology: Principles and applications, challenges and opportunities. Earth-Science Reviews. 2019;188: 77–107.