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Research Papers On Gladiators

Conscripts and volunteers

Today, the idea of gladiators fighting to the death, and of an amphitheatre where this could take place watched by an enthusiastic audience, epitomises the depths to which the Roman Empire was capable of sinking. Yet, to the Romans themselves, the institution of the arena was one of the defining features of their civilisation.

Hardly any contemporary voices questioned the morality of staging gladiatorial combat. And the gladiators' own epitaphs mention their profession without shame, apology, or resentment. So who were these gladiators, and what was their role in Roman society?

The Romans believed that the first gladiators were slaves who were made to fight to the death at the funeral of a distinguished aristocrat, Junius Brutus Pera, in 264 BC. This spectacle was arranged by the heirs of the deceased to honour his memory.

Gradually gladiatorial spectacle became separated from the funerary context, and was staged by the wealthy as a means of displaying their power and influence within the local community. Advertisements for gladiatorial displays have survived at Pompeii, painted by professional sign-writers on house-fronts, or on the walls of tombs clustered outside the city-gates. The number of gladiators to be displayed was a key attraction: the larger the figure, the more generous the sponsor was perceived to be, and the more glamorous the spectacle.

Most gladiators were slaves. They were subjected to a rigorous training, fed on a high-energy diet, and given expert medical attention. Hence they were an expensive investment, not to be despatched lightly.

For a gladiator who died in combat the trainer (lanista) might charge the sponsor of the fatal spectacle up to a hundred times the cost of a gladiator who survived. Hence it was very much more costly for sponsors to supply the bloodshed that audiences often demanded, although if they did allow a gladiator to be slain it was seen as an indication of their generosity.

Remarkably, some gladiators were not slaves but free-born volunteers. The chief incentive was probably the down-payment that a volunteer received upon taking the gladiatorial oath. This oath meant that the owner of his troupe had ultimate sanction over the gladiator's life, assimilating him to the status of a slave (ie a chattel).

Some maverick emperors with a perverted sense of humour made upper-class Romans (of both sexes) fight in the arena. But, as long as they did not receive a fee for their participation, such persons would be exempt from the stain of infamia, the legal disability that attached to the practitioners of disreputable professions such as those of gladiators, actors and prostitutes.

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Rules and regulations

Mosaic of fighting gladiators  © Regardless of their status, gladiators might command an extensive following, as shown by graffiti in Pompeii, where walls are marked with comments such as Celadus, suspirium puellarum ('Celadus makes the girls swoon').

Indeed, apart from the tombstones of the gladiators, the informal cartoons with accompanying headings, scratched on plastered walls and giving a tally of individual gladiators' records, are the most detailed sources that modern historians have for the careers of these ancient fighters.

Sometimes these graffiti even form a sequence. One instance records the spectacular start to the career of a certain Marcus Attilius (evidently, from his name, a free-born volunteer). As a mere rookie (tiro) he defeated an old hand, Hilarus, from the troupe owned by the emperor Nero, even though Hilarus had won the special distinction of a wreath no fewer than 13 times.

Attilius then capped this stunning initial engagement (for which he himself won a wreath) by going on to defeat a fellow-volunteer, Lucius Raecius Felix, who had 12 wreaths to his name. Both Hilarus and Raecius must have fought admirably against Attilius, since each of them was granted a reprieve (missio).

It was the prerogative of the sponsor, acting upon the wishes of the spectators, to decide whether to reprieve the defeated gladiator or consign him to the victor to be polished off. Mosaics from around the Roman empire depict the critical moment when the victor is standing over his floored opponent, poised to inflict the fatal blow, his hand stayed (at least temporarily) by the umpire.

The figure of the umpire is frequently depicted in the background of an engagement, sometimes accompanied by an assistant. The minutiae of the rules governing gladiatorial combat are lost to modern historians, but the presence of these arbiters suggests that the regulations were complex, and their enforcement potentially contentious.

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Fighting-styles

A Murmillo helmet  © The rules were probably specific to different styles of combat. Gladiators were individually armed in various combinations, each combination imposing its own fighting-style. Gladiators who were paired against an opponent in the same style were relatively uncommon.

One such type was that of the equites, literally 'horsemen', so called because they entered the arena on horseback, although for the crucial stage of the combat they dismounted to fight on foot.

Some of the most popular pairings pitted contrasting advantages and disadvantages against one another. Combat between the murmillo ('fish-fighter', so called from the logo on his helmet) and the thraex or hoplomachus was a standard favourite.

The murmillo had a large, oblong shield that covered his body from shoulder to calf; it afforded stout protection, but was very unwieldy. The thraex, on the other hand, carried a small square shield that covered only his torso, and the hoplomachus carried an even smaller round one.

Instead of calf-length greaves, both these types wore leg-protectors that came well above the knee. So the murmillo and his opponent were comparably protected, but the size and weight of their shields would have called for different fighting techniques, contributing to the interest and suspense of the engagement.

The most vulnerable of all gladiators was the net-fighter (retiarius), who had only a shoulder-guard (galerus) on his left arm to protect him. Being relatively unencumbered, however, he could move nimbly to inflict a blow from his trident at relatively long range, cast his net over his opponent, and then close in with his short dagger for the face-off.

He customarily fought the heavily-armed secutor who, although virtually impregnable, lumbered under the weight of his armour. As the retiarius advanced, leading with his left shoulder and wielding the trident in his right hand, his shoulder-guard prevented his opponent from striking the vulnerable area of his neck and face.

Not that all gladiators were right-handed. A disconcerting advantage accrued to the left-handed; they were trained to fight right-handers, but their opponents, unaccustomed to being approached from this angle, could be thrown off-balance by a left-handed attack. Left-handedness is hence a quality advertised in graffiti and epitaphs alike.

Originally the different fighting-styles must have evolved from types of combat that the Romans met among the peoples whom they fought and conquered - thraex literally means an inhabitant of Thrace, the inhospitable land bordered on the north by the Danube and on the east by the notorious Black Sea.

Subsequently, as the fighting-styles became stereotyped and formalised, a gladiator might be trained in an 'ethnic' style quite different from his actual place of origin.

It also became politically incorrect to persist in naming styles after peoples who had by now been comfortably assimilated into the empire, and granted privileged relationships with Rome. Hence by the Augustan period the term murmillo replaced the old term samnis, designating a people south of Rome who had long since been subjugated by the Romans and absorbed into their culture.

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Barrack life

The gladiatorial barracks were marked by heterogeneity. Membership was constantly fluctuating, as troupes toured the local circuit. Some members survived to reach retirement; new recruits were enlisted, many of them probably unable to understand Latin.

In the larger barracks, members of the same fighting-style had their own dedicated trainer, and they often bonded together in formal associations. Frequently it was a gladiator's fellows who furnished his tombstone, perhaps through membership of a burial society.

Yet gladiators must frequently have met their intimate fellows in mortal combat. Professionalism and the survival instinct would have demanded a merciless display of expertise, inculcated by the gladiator's training. Within a training-school there was a competitive hierarchy of grades (paloi) through which individuals were promoted.

The larger barracks, at least, had their own training arena, with accommodation for spectators, so that combatants became accustomed to practising before an audience of their fellows. The system meant that combat and heroic prowess were brought right into the urban centres of the Roman empire, whereas real warfare was going on unimaginably far away, on the borders of barbarism.

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Criticism and popularity

A Roman mosaic showing amphitheater scenes  © There were some dissenting voices: the philosopher-emperor Marcus Aurelius found gladiatorial combat 'boring', but he nevertheless sponsored legislation to keep costs at a realistic level so that individuals could still afford to mount the displays that were an obligatory requirement of certain public offices.

Both pagan philosophers and Christian fathers scorned the arena. But they objected most vociferously not to the brutality of the displays, but to the loss of self-control that the hype generated among the spectators.

Gladiatorial displays were red-letter days in communities throughout the empire. The whole spectrum of local society was represented, seated strictly according to status. The combatants paraded beforehand, fully armed. Exotic animals might be displayed and hunted in the early part of the programme, and prisoners might be executed, by exposure to the beasts.

As the combat between each pair of gladiators reached its climax, the band played to a frenzied crescendo. The combatants (as we know from mosaics, and from surviving skeletons) aimed at the major arteries under the arm and behind the knee, and tried to batter their opponent's skull. The thirst for thrills even resulted in a particular rarity, female gladiators.

Above all, gladiatorial combat was a display of nerve and skill. The gladiator, worthless in terms of civic status, was paradoxically capable of heroism. Under the Roman empire, his job was one of the threads that bound together the entire social and economic fabric of the Roman world.

Not even Spartacus, most famous of all gladiators, has left his own account of himself. But shreds of evidence, in words and pictures, remain - to be pieced together as testimony of an institution that characterised an entire civilisation for nearly 700 years.

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Citation: Lösch S, Moghaddam N, Grossschmidt K, Risser DU, Kanz F (2014) Stable Isotope and Trace Element Studies on Gladiators and Contemporary Romans from Ephesus (Turkey, 2nd and 3rd Ct. AD) - Implications for Differences in Diet. PLoS ONE 9(10): e110489. https://doi.org/10.1371/journal.pone.0110489

Editor: Clark Spencer Larsen, Ohio State University, United States of America

Received: June 13, 2014; Accepted: September 16, 2014; Published: October 15, 2014

Copyright: © 2014 Lösch et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All relevant data are within the paper.

Funding: The study was funded internally by the Department of Forensic Medicine at University of Medicine Vienna. There were no other individuals employed or contracted by the funder than the named authors. Therefore no one other than the authors played any role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

There are various archaeological publications about the unique cultural phenomenon of Roman gladiators [1], [2], [3], [4], [5], [6], [7], [8], [9] as well as artifacts associated with them [10], [11], [12], though the recovery of human remains from gladiators is extremely rare [13], [14]. Alleged arena fighters were found only at a few excavation sites: Pompeii in Italy [15], Eboracum (York, UK) [16], Augusta Treverorum (Trier, Germany) [17], and Colonia Augusta Aroe Patrensis (Patras, Greece) [18]. However, the verification of these findings remains uncertain. In 1993, a gladiator cemetery was discovered in Ephesus, Turkey [19] (Figure 1a). Most individuals from this site exhibited trauma which supports the assumption that they were gladiators [13], [14]. The trauma pattern confirms what written sources mention about the rules for gladiator fights.

Figure 1. Study area at the west coast of Turkey.

(a) Geographical location of ancient Ephesus. (b) City map of Roman Ephesus with investigated excavations sites. (c) Details of the excavation trench in 1993 (DAM93) including the gladiator cemetery (DAM93G). Images compiled with modified data from OpenStreetMap and CIA maps.

https://doi.org/10.1371/journal.pone.0110489.g001

Historical sources report that socially stratified Roman populations had diverse nutrition. Recently, several isotope analyses were conducted on human bones from Roman times, especially from Italy [20], [21], [22], [23], [24], Croatia [25], Britain [16], [26], [27], [28], Tunisia [29], and Egypt [30], [31], [32]. In contrast, little isotopic work has been done on skeletal series from the geographic region of Turkey [33], [34], [35], [36], [37]. Contemporary Roman texts mention that gladiators consumed a specific diet called “gladiatoriam saginam”, which included barley and bell beans (vicia faba) [38], [39]. Their consumption of barley led to the derogatory nickname “hordearii” (barley eaters) [40]. Presuming the historical reports on gladiator diet habits were accurate, it might be possible to detect differences in stable isotope and/or trace element ratios in bones of gladiators and contemporary “ordinary” Romans. Therefore, the aim of this study was to reconstruct possible diet restrictions of gladiators in comparison to contemporary inhabitants of Roman Ephesus. Stable isotopes (C, N, S) and the inorganic bone compounds (Sr, Ca) were investigated to obtain information about nutrition and social stratification.

Stable isotope analysis

Stable light isotope ratio analysis of bone collagen is an established method in bioarchaeology. It reveals important information about nutrition, life history, and migration in past populations [41], [42], [43], [44], [45]. Bones and teeth are the most commonly preserved human tissues in the archaeological record. Collagen is the main protein in bone that provides the source for organic carbon (13C/12C), nitrogen (15N/14N) and to a lesser extent sulphur (34S/32S). Because bone is a living tissue that turns over regularly within the lifetime of an individual, isotope ratios reflect average values.

The analysis of stable carbon isotopes provides important information about plant consumption. Due to fractionation, the consumer's δ13C value is enriched by +5‰ when vegetable food is metabolised. Stable carbon isotope ratios in bone collagen are analysed to differentiate between individuals with higher intake of C3 (e.g. wheat, barley) and C4 (e.g. millet, maize) plants which differ in their photosynthetic pathway [41], [46], [47].

Stable nitrogen isotopes in bone collagen reflect the intake of animal protein, especially meat and dairy products. Like stable carbon isotope ratios, the δ15N values also give information about the trophic level. Due to fractionation the approximate shift is about +3‰ to +5‰ in bone collagen [43], [48]. In an ecosystem, the δ15N value increases towards the top of the food chain.

The analysis of the bone collagen sulphur isotope ratio as a multiple isotopic approach can shed light on additional aspects of ancient populations' diets [49]. The δ34S in bone collagen is passed along the food chain with a small fractionation of approximately −1‰ and directly reflects the δ34S values of the consumed food [27], [37]. Compared to freshwater and terrestrial environments, there is a very high concentration of compounds containing sulphur in the ocean [50]. δ34S values in freshwater and terrestrial ecosystems range from −22‰ to +22‰ [51], [52]. Terrestrial mammals have δ34S values lower than +10‰, whereas organisms in marine ecosystems have values around +20‰ [53]. The “sea spray effect” describes the high amount of marine sulphates in coastal regions and islands as a result of evaporation and rainfall [54]. Unlike carbon and nitrogen isotope analysis, δ34S in ancient bone collagen is addressed in only few publications [27], [51], [52], [53], [54], [55], [56], [57], [58]. Therefore, few comparative data are available for this study.

Trace element analysis

Through analysis of the inorganic mineral of bone – mainly a bio-apatite similar to the more crystalline hydroxyapatite – it should be possible to identify the main Ca supplier in the diet [59] through its specific Sr/Ca-ratio which can be reconstructed from the Sr/Ca ratios found in bone.

Sr and Ca behave similarly in building up the hydroxyapatite in the mineral bone fraction due to their similar chemical properties. The pathways of Sr in biological systems and especially in the food web have been thoroughly investigated because of concerns regarding the biological effects of radioactive Sr-90 fallout caused by atmospheric nuclear tests in the 1950s and 1960s [60], [61], [62], [63], [64]. As a result, the Sr metabolism and the Sr distribution in various organisms are well known. It has been shown that Sr serves no known metabolic function. Compared to Ca, the uptake of Sr into the body underlies discriminating restrictions during its passage from the digestive tract into the bloodstream. Mammals absorb only 20–30% of the Sr intake, but once in the body, virtually the entire amount of Sr accumulates in bone and teeth as a substitute for Ca in the apatite lattice [60], [65], [66], [67], [68]. Due to the preferred uptake of Ca compared to Sr and the resulting “biopurification” of Ca in the food chain, it was long believed that Sr functions as a dietary plant-to-meat ratio indicator [67]. It was assumed that a high Sr amount in the bone reflected a high vegetarian intake, and a low Sr amount indicated a diet rich in meat. Therefore, studies of Sr/Ca-ratios for the reconstruction of diet were introduced in 1965 for extinct animals and in the 1970s and early 1980s for prehistoric humans [69], [70], [71], [72], [73], [74], [75]. Since then, numerous studies have dealt with this subject. Thus, we refer to detailed review articles(e. g. by [76], [77], [78], and [59]). Two major issues with this concept of diet reconstruction have to be highlighted:

First, the dietary plant-to-meat ratio approach experienced a major correction by Burton and Wright [79]. They showed that Sr/Ca ratios in bone reflect the Sr/Ca ratio of the strongest Ca supplier rather than the whole plant-to-meat ratio of a multicomponent diet. This limits future Sr/Ca studies to identifying the major Ca source of the diet.

A second major drawback for the investigation of trace elements arose from the fact that bones buried in soil undergo diagenetic alterations [59], [80]. Many attempts were made to identify and quantify diagenetic changes to Sr/Ca-ratio with the target to reconstruct original Sr/Ca-ratios (summarized in [59]). Because of the complexity and variability of soil processes, this seems impossible up to now. Therefore, the scientific focus has shifted from trace elements to stable isotopes for diet reconstruction in recent years. Only few combined studies on trace elements and stable isotopes are available. Though we believe that trace element and stable isotope investigations complement each other and have the potential to draw a more comprehensive picture of ancient diets.

Gladiators

The social group of gladiators mainly consisted of prisoners of war, slaves, and condemned offenders. The Roman jurisdiction had two judgements that forced people to fight in the arena [8]. Contestants with swords (ad gladium) had to fight in the arena without prior special training, which in most cases meant certain death. Gladiator school participants (ad ludum) got appropriate training and education. They could prove their ability for social reintegration in the course of the fights. There were also “volunteer” gladiators regardless of the about 1∶9 probability of dying in a gladiator fight in the 1st century AD [81]. Common citizens, senators, noblemen, and even emperors could pursue training in gladiator schools (ludus). Thus, the occupational group of gladiators probably consisted of males from almost all social groups of the Roman society [8], [81]. Therefore, occupational group here refers to participants of the gladiator school.

Gladiator fights as a socially institutionalized spectacle represent a unique phenomenon in human history. Ancient texts, ceramic artefacts, and iconography were subjected to scientific, archaeological, and historical investigation for a better understanding of gladiator fights and their cultural and social context in ancient Roman society [1], [2], [4], [5]. In recent years, additional data about the use of weaponry and protective gear were collected through experimental archaeological studies [9].

For Ephesus, gladiator fights are reported since 69 BC when they were held under the auspices of the Roman governor Lucullus [82]. Artefacts, mainly oil lamps and graffiti with fighter illustrations, suggest that gladiator fights became increasingly important over time and peaked out in the 2nd and 3rd century AD when Ephesus was the capital of the province Asia.

Materials and Methods

Ethics Statement

All necessary permits for the excavations, sampling, shipping and conducted analyses were obtained from the legal representative (Directorate-General for Antiquities and Museums of Ankara, Turkey).

Sampled humans

Human remains from the gladiator cemetery (DAM93G) and from the three other excavation complexes marked as DAM92, DAM93NG, and DAM94 were examined (Fig. 1b). The excavations were conducted between 1992 and 1994. The complexes date to the 1st to 3rd century AD, the gladiator cemetery in particular dates to the 2nd to 3rd century AD [82]. Detailed information is given in the excavation reports [83], [84] and in the anthropological reports [85], [86], [87], [88]. The burial sites DAM93G and DAM93NG are located at the northern foot of the Panayırdağ hill about 300 m east of the ancient stadium, between a procession route and an ancient road (Fig. 1b). The human samples from DAM93NG derive from 8 female and 8 male individuals unearthed in 1993 in direct proximity to the gladiator cemetery. The excavation in the nearby “fig garden” revealed a sarcophagus filled with soil and remains of 3 females and 3 males (DAM92). At the opposite side of the Panayırdağ DAM94 was located and revealed burials of 7 females and 8 males in various sarcophagi.

DAM93G (the gladiator cemetery) mainly consisted of graves with plain walls and fixed tombstones with illustrations of different types of gladiators (Fig. 2). The human remains were found in an approximately 3 m thick layer in a 20 m2 area (Fig. 1c). Commingled bones indicate that the site was used multiple times over an extended period [83]. Therefore, the documentation and recovery of human remains were carried out according to mass grave excavation methods [89], [90]. The morphologic-anthropological examination of the individuals' sex and age was performed as per [91], [92], [93], [94], [95] and [96]. 53 individuals were analyzed for stable isotope ratios and 35 individuals for Sr/Ca-ratios (Table 1).

The sample ID (e.g. EPH-DAM 155/93 rFEM 2), consists of EPH for the location Ephesus, DAM for the excavation site Damianosstoa, 155 is the storage box number, 93 means the excavation year 1993 and rFEM-2 stands for the second right femur in this storage box. Retaining subsamples are stored at the Department of Forensic Medicine in Vienna. The remaining bones are labelled and saved in storage boxes in the sealed depot of the excavation house of the Austrian Archaeological Institute in Ephesus (Atatürk Mah., 1064 Sok., No 13, TR-35920 Selçuk/İzmir, Turkey).

Sample for trace element diagenesis control

For investigation of diagenetic alterations of Sr/Ca-ratios, additional samples of cremated human bones and soils were taken. About 18 kg of cremated human bones from two large Pithoi (DAM93P) were available for investigations. Both of these ceramic containers, Pithos I (EPH-DAM-P-I/93) and Pithos II (EPH-DAM-P-II/93), were found in close proximity to the gladiator cemetery (Fig. 1c). Anthropological investigations revealed that at least 3 females and 13 male were cremated, and the remaining bone and teeth fragments were subsequently filled into the two Pithoi [87], [97]. A subsample of about 200 g of femur fragments from each Pithos was taken and homogenized to get a representative and average sample for all buried individuals.

Soil samples were retrieved from all four excavation locations (DAM92, DAM93G, DAM93NG, DAM94). Since during the initial excavations no chemical studies were planned, systematic sampling, such as taking complete soil columns, was not carried out. Retrospectively, it was possible to get soil from the inner lumen of the bones. Specimen identifiers were given according to the system used for the human remains with the ending SOIL (e.g. in EPH-DAM92-SOIL) (Table 2).

Table 2. Data of calcium (Ca); Ca/P-ratios, strontium (Sr), and Sr/Ca-ratios, as well as lanthanum (La) and pH for the analyzed samples of animal and cremated human bones respectively total soil and soil eluents.

https://doi.org/10.1371/journal.pone.0110489.t002

Collagen extraction and stable isotope ratios measurement

All samples were cleaned with distilled water and ground to bone powder. The collagen extraction followed the [98] and [41] procedure. 500 mg samples were treated with 1 M HCl to dissolve the bone mineral and then rinsed until neutral. To remove humic and fulvic acids, the samples were treated with 0.125 NaOH and gelatinized in warm 0.001 M HCl at 90°C for 17 h. Then, the samples were filtered and freeze-dried. The lyophilized collagen was weighed three times in tin capsules. Stable isotope ratios of carbon (13C/12C), nitrogen (15N/14N), and sulphur (34S/32S) were analysed by isotope ratio mass spectrometry (IRMS at Isolab GmbH). The mean value of all three measurements was calculated, and an internal standard was used to determine the analytic error. The data are presented in δ-notation in per mil (‰) relative to international defined standards for carbon (Vienna Pee Dee Belemnite, VPDB), nitrogen (Ambient Inhalable Reservoir, AIR), and sulphur (Canyon Diablo Troilit, CDT). The analytical error amounted to ± 0.1‰ for δ13C, ± 0.2‰ for δ15N and ± 0.3‰ for δ34S.

Collagen quality control.

The collagen quality was verified as per [99], [41] and [100]. Collagen extracts with less than 1% collagen in proportion to their dry weight and data, with a molar C/N relation outside a 2.9–3.6 range were not taken into consideration. %C and %N values (43% and 15–16%) that strongly deviate from recent collagen values were also not taken into consideration.

Trace element sample preparation and measurements

The bone sample preparation followed a protocol developed for spectroscopic trace element analysis in bone or teeth [101], [102], [103]. First, the bones were superficially cleaned with tap water and dried at room temperature. Available bones were sampled with a diamond-coated trepanation drill. Pieces of compact bone were cleaned with distilled water and degreased with diethylether. To remove possible diagenetic contaminations, specimens were etched for 4 min with concentrated formic acid and then washed with distilled water in an ultrasonic bath following the decontamination protocol by [104], respectively [105]. After drying and homogenisation in agate mortar, an aliquot of approximately 500 mg bone powder was ashed at 500°C for 12 h and wet-digested under pressure for 6 h at 110°C with 1.5 ml concentrated nitric acid in a Teflon bomb.

Additionally, bone drilling wastes were collected for each group and homogenised aliquots were checked for the presence of Lanthanum (La). It turned out that for all drill waste samples the concentration of La was below the limit of detection (0.09 µg/g). Therefore, 100 µg La were added as internal standard to the resulting digestions of all bone samples and filled up to a final volume of 20 ml with bi-distilled H2O. After a final dilution (1∶100), strontium, calcium and phosphorus were measured in triplicates by ICP-OES (Perkin Elmer Optima 3000XL) under optimized conditions (see below and [103]).

Soil sample preparation.

For the soil pH determinations, 50 g of dry soil were placed in a conical flask (250 mL) and 100 ml of bi-distilled water was added and the flask was shaken for 2 minutes. The resulting suspension was allowed to set for about one hour until the pH electrode in the supernatant showed stable values (DIN ISO 10390) which were recorded. Subsequently, the supernatant was decanted and measured by ICP-OES to investigate soil leaching abilities occurring during the presence of rain water.

For the total digestion of soil samples, lithium metaborate fusion according to [106] was applied. 100 mg of dry soil was mixed with 500 mg lithium metaborate (LiBO2), transferred to a pre-ignited high-purity graphite crucible, and placed in the muffle furnace at 950°C for 15 min. The molten material was subsequently transferred into a Teflon beaker filled with 50 ml of 1N nitric acid and stirred until solution was completed. The solution was transferred to a volume flask and filled up to 100 ml with bi-distilled water and measured by ICP-OES.

Instrumentation characteristics for ICP-OES measurements.

Spectral lines free of interferences were selected. The linear working ranges were investigated to determine the necessary dilutions for the measurements. Limits of detection (LOD) for each element were calculated by tripling the standard derivation of 11 measurements of the blank divided by the slope of the corresponding calibration curve. International reference standards SMR1486 (bone meal) and SMR2711 (Montana soil) were analyzed to monitor precision and accuracy of the sample pretreatment and ICP-OES measurements. The selected spectrometer wavelengths, necessary dilutions and the LODs for the bone samples, as well as the precisions and accuracies for bone and soil samples are given in Table 3.

Since the accuracy turned out be lower than 2% for Ca, P and Sr in bone and soil, and the precision for determination of all elements was less than 3%, significant variation of actual differences in bone concentrations can be identified if they are greater than 3%.

Statistical tests

Due to the sample size, the non-parametric Kruskal-Wallis test (3 parameters) and Mann-Whitney-U test (2 parameters) for independent samples were performed (SPSS Statistics 20). The aim was to detect evidence against the null hypothesis that there is no difference between the gladiators and the contemporary Romans.

Results

Bone samples

Bone samples of 22 males from the gladiator cemetery (DAM93G) were analysed (Table 1). After the extraction, two samples were excluded due to insufficient collagen quality [41], [99], [107], [108]. Additionally, samples of 31 non-gladiator (NG) individuals (15 males, 8 females, 8 infants) from the complexes DAM92, DAM93NG, DAM94 were analysed, and had to be reduced to 20 samples (13 males, 4 females, 3 infants) due to quality control or insufficient collagen detection. Until now, hardly any collagen quality criteria for sulphur isotope analysis have been published [109]. All δ34S values were evaluated for this study except those from the individuals that were excluded due to the aforementioned collagen quality control criteria.

For the Sr/Ca bone mineral analysis, only the mid-shaft compacta of adult individuals' femora and humeri were sampled since the turnover rates of the diaphyseal regions of these long bones are similar and therefore comparable [103]. This reduced the initial sample size for the gladiators to 21 males and for the non-gladiators (NG) to 11 males and 3 females.

The gladiator samples show mean values of −18.9±0.4‰ for δ13C, 9.3±0.8‰ for δ15N and 7.5±1.9‰ for δ34S. The mean values of the NG- male samples are −19.0±0.2‰ for δ13C, 9.4±0.6‰ for δ15N and 7.3±1.1‰ for δ34S. In the female samples, the mean values are −18.9±0.5‰ for δ13C, 8.9±1.1‰ for δ15N and 7.2±3.0‰ for δ34S, whereas the infant samples show mean values of −19.0±0.2‰ for δ13C, 9.0±0.7‰ for δ15N and 6.9±1.6‰ for δ34S (Table 4).

The non-parametric Kruskal-Wallis test for unpaired groups on the gladiators and the contemporary males and females shows no significant difference in the mean δ13C (asymptotic p = 0.828), δ15N (asymptotic p = 0.850) and δ34S (asymptotic p = 0.668) values for the contemporary individuals. Therefore, all NG adults (male and female) were subsequently tested against the gladiators by the non-parametric Mann-Whitney-U test for unpaired groups (Table 5). This revealed no significant differences (asymptotic p for δ13C = 0.986, δ15N = 0.957, δ34S = 0.478).

The gladiators' Sr/Ca data show a mean value of 1.26±0.33 µg/mg. The NG male samples have a mean value of 0.68±0.10 µg/mg and the females of 0.65±0.02 µg/mg. Samples of infants were not analysed for Sr/Ca.

The non-parametric Mann-Whitney-U test for unpaired groups on the (male) gladiators and the NG males and females reveals in the first step that there is no significant difference between the mean Sr/Ca (p = 0.586) for the NG male and female sub-samples. Therefore, the NG males and females are pooled (0.67±0.09 µg/mg) to increase the sample size and then tested against the gladiator group. This reveals a highly significant difference between the Sr/Ca-ratio means (p<0.001) of the gladiators and the NG inhabitants (Table 5).

Cremated human bone and soil samples

Results for the other analyzed samples are given in Table 2. Resulting ratios for Ca, Sr respectively Sr/Ca for mean bone, total soil and soil eluent gradients are given in Table 6.

Table 6. Ratios of Ca and Sr for bone vs. total soil vs. soil eluent and bone vs. soil eluent gradients, as well as Sr/Ca-ratios in bone, soil and eluent for all investigated excavation locations.

https://doi.org/10.1371/journal.pone.0110489.t006

The bone samples from the cremations out of Pithos I and II showed Sr/Ca-ratios of 0.58 µg/mg respectively 0.61 µg/mg, which are comparable to the Sr/Ca-ratios found in bones of the non-gladiator group (0.67±0.09 µg/mg).

Differences in the element content of the total soil samples were found. Specifically, Ca in the samples from the DAM93 location was only about half of what it was at the other two locations. The Sr concentrations in the DAM93 soils were similar (DAM93G = 122.4 µg/g and DAM93NG = 102.7 µg/g), but significantly lower than the concentrations in the soils of DAM92 (171.5 µg/g) and DAM94 (196.5 µg/g). Both of these findings together result in higher Sr/Ca-ratios for the soil of the DAM93 (2.15 µg/mg and 2.43 µg/mg) location compared to DAM92 (1.50 µg/mg) and DAM94 (1.61 µg/mg). For all four soils a heterogeneous distribution of P was evident by Ca/P ratios varying from 11.1 to 47.1. Finally, La was present in all soil samples at similar concentrations of about 50 µg/g.

The bi-distilled water elution of the soil samples revealed low and similar alkaline pH values for all four soils, ranging from 7.14 to 7.72. Nevertheless, the pH values for the DAM93 soils (pH 7.72 and pH 7.66) turned out to be slightly higher than for the DAM92 soil (pH 7.30) and DAM94 soil (pH 7.14). In the eluent, Ca concentrations of 535.8 µg/L for DAM93G, 479.3 µg/L for DAM93NG, respectively 868.9 µg/L for DAM92 and 875.4 µg/L for DAM94, were found.

The results reveal that about 1% of the Ca content of the DAM93 soils (DAM93G = 0.94%; DAM93NG = 1.14%) was eluted, whereas only 0.76% (DAM92) respectively 0.72% (DAM94) was depleted from the two other soils (Table 6).

The Sr concentrations in the eluent of the soils were 1.52 µg/L for DAM93G and 1.46 µg/L for DAM93NG, 2.92 µg/L for DAM92 and 2.78 µg/L for DAM94. These values indicate that the relative amount of Sr depleted was similar and on average approximately 1.5% of the total soil content. In other words, about the same relative amount of Sr can be depleted from all soils, but the relative depletion rate is slightly higher than the depletion rates for Ca. Especially the different depletion of Ca from the soils produces higher and finally more homogenous Sr/Ca-ratios in the eluent, as they were evident in the total soil. Specifically, in the eluent, an average Sr/Ca-ratio of 3.11±0.22 µg/mg, ranging from 2.84 µg/mg to 3.36 µg/mg was observed, whereas in the total soil the average Sr/Ca-ratio was 1.92±0.44 µg/mg (1.50 µg/mg to 2.43 µg/mg).

For the ratios of total soil versus bone, respectively, soil versus eluent and the direct ratios of eluent versus bone, it was found that the concentrations of Ca were at least 3 times higher in the bones than in the soils, and for DAM93NG even 8.53 times higher. The Sr concentrations in bone were higher than in the surrounding soils for all four locations, but the gradients were lower than for Ca, about 3 times for the DAM93 locations and a bit less than 1.5 times for DAM92 and DAM94.

The bone to eluent ratios are the most interesting ones, since they reflect similar ratios as those that would have occurred when (rain-)water was present to immerse the buried bone for a certain time. About 400 times more Ca was found in the bones of DAM92 and DAM94, and about 700 times higher Ca concentrations in the bones from the DAM93 locations. The Sr ratios turned out to be lower than the Ca ratios again, about 100 times for the DAM92 and DAM94 locations and 150 times for DAM93NG, respectively 300 times for DAM93G. It is obvious that, although the absolute Sr concentration for both DAM93 elutions is more or less the same (1.52 µg/L and 1.46 µg/L), the differences in the bone-eluent ratios (approx. 300 respectively 150) arise from significant differences in the Sr concentrations of the bones.

Discussion

Stable isotopes

The different groups' stable isotope data (gladiators, NG males/females) do not differ significantly. The sulphur isotope ratios show the greatest and the carbon ratios the lowest standard deviation.

Carbon

All individuals consumed C3 plants like wheat and barley as staple food. Pliny the Elder reported in his Naturalis historia that barley (hordearii), a C3 plant, was a main component of the gladiators nutrition which matches our findings [9]. However, most NG individuals apparently also had C3 plants as a staple food since no statistical difference is detectable. A few individuals show more positive δ13C values. The most probable cause for this is an increased consumption of C4 plants such as millet. Millet was an important nutrition crop in Eurasia and its consumption has already been verified in several ancient societies by stable isotope investigations [110], [111], [112], especially since the Middle Bronze Age in Italy [113]. [21] published similar δ13C data for imperial Rome Isola Sacra (−18.8‰ versus −18.9‰ here). They mention ancient literature in which millet is described as an animal food and as less desirable for human consumption under “normal” circumstances. In their study, the δ13C values of the faunal remains are more negative than those of the humans, so it was assumed that the terrestrial herbivores basically fed on C3 plants. Although animal bones have not been investigated yet for reference in our study, we agree with [21]. If the δ13C values were caused by the consumption of millet-fed animals, then higher δ15N values would be expected for the Ephesus population.

One of the individuals with a rather strong signal for C4 plants, a δ13C value of −17.8, belongs to the gladiator group (EPH-DAM 187/93 rFEM 6) (Fig. 3). Another gladiator (EPH-DAM 248/93 rFEM 6) and one female (EPH-DAM 72/93 rFEM-1) show at least hints for a mixed signal of C3 and C4 plants. This individual is also extraordinary as she was the only female to be found in the gladiator cemetery. This leads to two hypotheses: 1) these individuals had a different diet than the others or 2) they came from other geographical regions with a more C4 plant-based diet and migrated to Ephesus. The second one is more probable because the extensive cultivation of millet is only evidenced since the Early Byzantine Period, ca. AD450, for this region [33]. Comparable δ13C data from Roman North Africa (Tunisia) with a mean of −17.7‰ were published by [29]. However, their combined δ13C and δ15N values suggest a significant amount of dietary protein intake from marine resources.

It is hard to determine how long these individuals from other geographical regions had already lived in Ephesus. Due to collagen turnover in adult bones, the data reflect a mixed value from the final years or even decades of life. Female collagen turnover rates are on average 3–4% per year and reduce with increasing age, whereas for males they are only 1.5–3% per year [43]. Human bone collagen of e.g. femora reflects an individual's nutrition over a much longer time period than 10 years [43]. Most individuals from Ephesus were young adults between 20 and 30 years of age [88]. This also indicates that the three individuals with higher δ13C values grew up in other geographical regions and migrated to Ephesus.

Nitrogen

Compared to other Roman sites, the δ15N values of Ephesus are relatively low [16], [21], [23], [28], [29], [30], [33], [114]. The mean value of 9.3‰ is even lower than in Late Imperial Sagalassos (10.1‰, n = 3) but similar to Middle Byzantine Sagalassos (9.1‰, n = 42) in Turkey [33] – even though Sagalassos is far away from the sea and Ephesus is close to the Aegean Sea. Because of its proximity to the ocean and thus good access to seafood, much higher δ15N values were expected for Ephesus. Other samples from comparable archaeological Roman sites show a much stronger marine influence (e.g. Isola Sacra in Italy [21], [23] and Leptiminus in Tunisia [29]). The Roman coastal site Velia in southern Italy shows values similar to Ephesus [20]. An ancient cookbook written by Apicius which contains a collection of Roman recipes, suggests that seafood was probably consumed in Ephesus. Fish was most likely eaten as fish sauce (garum), but also cooked and salted.

The Ephesus δ15N values also indicate a generally minor consumption of animal proteins, like meat and dairy products. But the most probable cause for the depletion of 15N in Ephesus could have been a frequent consumption of legumes. [34] detected signs of human consumption of pulses in Neolithic Turkey. Archaeo-botanical analyses in Sagalassos, Turkey, show that peas and lentils were extensively cultivated since the Early-Middle Imperial Roman time from 25BC until 300AD [33] and even more in the Late Imperial Roman period.

Legumes generally have very low δ15N values due to their molecular nitrogen fixation by symbiotic bacteria which in turn might be reflected in the consumer's collagen. Presumably, the regular consumption of large amounts of pulses lowers human δ15N values considerably. Legumes are also rich in protein (up to 25%) and the availability of dietary protein influences the supply of essential amino acids. Wheat for example is short of lysine while beans are short of methionine. A combination of wheat and beans or of cereals and pulses can lead to a protein supply resulting in an availability of up to 90% [34].

Two individuals have much depleted δ15N values. One belongs to the gladiator group (EPH-DAM 128/93 rFEM 5) and the second is female (EPH-DAM 106/93 PAR-2). Both relatively low values could be the result of a regular consumption of legumes. Galen reported in his ancient text De alimentorum facultatibus that beans (vicia faba) were an important nutrition component for gladiators while they explicitly did not get much meat [115]. In contrast to this, the two individuals with the highest values are from the gladiator group, too (EPH-DAM 146/93 rFEM 1 and EPH-DAM 76/93 rFEM 2). That indicates a regular consumption of animal proteins and a lower intake of legumes. Within the gladiator group, the isotope data extend over more than one trophic level for δ15N but also for δ13C. This leads to the conclusion that the individuals from the gladiator cemetery were a very heterogeneous group who consumed different kind of foods.

Sulphur

There are only very few comparable sulphur isotope values from Roman sites. [58] investigated humans from a Bronze Age mass burial near Greek Thebes which showed a higher mean for δ34S (13.3‰) than the Ephesus individuals (7.4‰). [58] postulates that marine food was rare and that the Bronze Age diet at Thebes mainly derived from terrestrial resources. This could indicate that the individuals from Ephesus also did not consume much seafish or seafood even though the city was close to the Aegean Sea. There are no signs for a high sea-spray effect on the soil of Ephesus either [54], [55].

The female from the gladiator cemetery (EPH-DAM 72/93 rFEM-1) and one gladiator (EPH-DAM 248/93 rFEM 6) show extraordinary δ34S values of more than 10‰ (Fig. 4), another gladiator shows δ34S values close to 10‰ (9.7‰, EPH-DAM 187/93 r FEM 2). All other individuals have lower sulphur ratios which mean that they can basically be assigned to terrestrial ecosystems. Both individuals with values higher than 10‰ had probably migrated from another geographical region and/or they consumed more fish and seafood than the others [58]. Surprisingly both individuals also show different δ13C values. They are discussed above as potential immigrants to Ephesus.

Trace elements

Possible diagenetic alterations.

Bio-apatite is extraordinarily chemically reactive because of the living human organism's requirement for the quick regulation of critical elements in the blood [59]. Its good reactivity originates from its high porosity, and the amorphous nature of bio-apatite causes a faster turnover compared to the organic compartment of the bone during life. However, its reactivity does not cease immediately after death, thus making it suspicious for postmortem contaminations. These features of the bone make it susceptible to two main manners of postmortem contamination. Firstly, its high porosity fosters physical infiltration by the soil itself and physical salt deposit from soil solutions. Secondly, the amorphous nature of bio-apatite compared to high crystalline hydroxyl-apatite increases its solubility in wet environments. Additionally, various studies have shown that for all interesting elements contamination can occur in both directions either through enrichment from soil or from depletion to the soil [80]. These processes are unfortunately not unidirectional, furthermore dissolution, permineralization, groundwater replacement, and ion exchange can occur at the same site depending on (ground-)water availability. For this reason, straightforward evaluations of the contamination cannot be made [116]. In general, it seems that virtually all bones buried in soil are affected by some contamination, and so far it does not seem possible to reliably quantify these contaminations [80]. Nevertheless, studies on bone contaminations in various environments prompted tests to find out if massive contamination by the soil has occurred or not [59], [80]. Therefore, possible alteration of Sr/Ca values due to diagenetic changes must be considered in every trace element study.

All investigated human bones and soils were excavated at the foot of the same hill (Panyirdağ) and can be dated within a range of 300 years. We can assume a similar climatic and topographic environment resulting in comparable impact of temperature, rainfall, and ground water conditions for all of the specimens.

All bone samples appeared similar macroscopically with a good status of preservation. Only minor differences of the superficial coloring of the bones were recognized. The same was evident for the hardness of the bones, which could be observed during the homogenization of the bone samples in an agate mortar. On average, about a 15±3% loss of weight during 500°C ashing in the course of sample preparation was detected. This indicates that organic material, believed to be protective for the bone mineral fraction [59], [80], was still present in all of the bone samples.

No quartz residues were found in any of the digestions of bone samples, and measurable concentrations of La in the drill waste bone samples were absent, although La was available (approx. 50 µg/g) in all four investigated soils (Table 2). Presence of quartz and La that are not present in the living bone [117] would be possible predictors for diagenesis in bone due to infiltration of the surrounding soil [59].

However, the prediction of mineral quality is not as simple and straightforward as it is for soil infiltration. Some authors believe that the integrity of the remaining bio-apatite can be checked with the ratio of Ca/P that was found to be about 2.12–2.35 for fresh and archaeological, unaltered bone [102], [104], [118]. Archaeological bones with Ca/P ratios within this range should indicate that no major degradation due to octocalcium phosphate, brushite, whitlockite or significant contaminations with calcium carbonate have occurred. Therefore, a good state of preservation [59] can be assumed. In our study, all investigated bones had Ca/P ratios ranging from 2.16 to 2.35 and therefore meet up to this criterion.

The investigation of the surrounding soil offers more potential to predict significant diagenetic alterations to the Sr/Ca-ratios of the bone. The macroscopic characteristics of all four investigated soils were similarly of dry grey nature. The pH values fell into a range between pH 7.14 and pH 7.72 for all four soils. For soils with pH above 7.0, early trace elements studies postulated that they are less prone to diagenetic alterations of bone than acidic soils (pH<7.0). Nevertheless, [80] found on bones from alkaline soil that they may act as Sr sponges and are able to accumulate Sr to values even higher than 1000 µg/g (mean  =  879 µg/g; max  =  1488 µg/g), although the values for Sr in the surrounding soil were lower. Such extraordinarily high Sr values were not found in or study. Overall we found a mean Sr concentration of 373.9 µg/g, with individual values ranging from 195.6 µg/g to 724.9 µg/g.

The significantly lower Ca values in the DAM93 soil and therefore the much higher Sr/Ca-ratios in this soil raises concerns whether these conditions caused diagenetic alterations of the bones at this location. But, there are still significant differences in the Sr/Ca-ratios between gladiators (1.26±0.33 µg/mg) and non-gladiators (0.63±0.08 µg/mg) from the DAM93 site buried close to each other. Further, our leaching experiments with bi-distilled H2O (simulating rain water) for the different soils have shown that although there were great variations in the Sr/Ca-ratios within the different bones and within the different soils, the H2O eluents of all four soils turned out to have similar Sr/Ca-ratios, ranging from 2.84 to 3.36 µg/mg (Table 2). [119] studied the ability of bovine bone meal to act as decontamination sorbent for Sr90

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