Ancient ceramic amphorae

Analysis of organic residues for archaeology

By combining cutting-edge technologies such as infrared spectrometry, Raman spectrometry and chromatography, our scientists are able to detect and identify the organic remains found in ancient amphorae and pottery. The techniques developed by CIRAM enable us to characterize oils, fermented beverages, resins, fats and perfumes, so as to understand the dietary and cosmetic habits of ancient peoples.

Organic residues: understanding old habits and practices

Organic residues found in dishes, vases and flasks provide clues to food customs and ancient cooking methods, for example. But they can also provide information about trade in Antiquity or the Middle Ages, as well as ancestral burial practices. CIRAM laboratories have an analytical network that covers a wide spectrum of investigations, from the identification of major product families (oil, fat, resin, etc.) to the discovery, in the best of cases, of ancient cooking recipes.

Organic residue analysis methods

Fourier transform infrared spectroscopy, in ATR mode or under microscopy, is used to identify the major families of organic compounds. For example, the presence of oil, animal fat or natural resin can be characterized. Mineral matter, however, can provide a spurious signal, preventing identification of the organic compounds present. For this reason, infrared spectrometry will usually be used as a preliminary step. CIRAM teams will generally couple FTIR spectrometry with other analysis techniques, such as chromatography or Raman spectrometry.

GC-MS coupling to locate and identify substances

Gas chromatography (GC) coupled with mass spectrometry (MS) is the technique dedicated to the study of organic compounds. Chromatography separates compounds in a sample, while mass spectrometry identifies compounds according to their mass. This GC-MS coupling enables the precise identification and quantification of many substances present in very small quantities, or even in trace amounts. Using GC-MS analysis, our scientists can characterize most of the molecules present in an archaeological mixture or organic residue. It is the nature of these molecules, combined with their concentration, that enables us to trace them back to the material used: olive oil, walnut starch, animal fat, tannin...

Complementary analytical techniques for the analysis of certain residues

Although Raman spectrometry is more suited to the study of mineral matter, it is nonetheless an interesting method for archaeometry, as it is non-invasive and requires no sample pre-treatment.

This analysis provides very good spatial resolution, making it possible to study samples on a very small scale (spots of a few µm). Raman spectrometry can be used on its own, or in conjunction with FTIR spectrometry or GC-MS chromatography. In fact, the residues found in ancient pottery are so complex that it is generally necessary to use different complementary analytical techniques.

Carpology for the study of seeds and fruits that have been discovered

Carpology is the study of seed and fruit remains found in ancient containers or archaeological sediments. Analysis of these plant residues provides information on human activities and ancestral lifestyles. Even when charred, CIRAM scientists are able to identify the nature of these seeds, and thus understand their use and reconstruct environments.

Palynology, the study of pollen and spores

Palynology is the study of pollen and spores released by plant species. Coupled with carpology and anthracology, these techniques enable us to reconstruct environments and climates. Observations made using light microscopy or electron microscopy will make it possible to determine the size and shape of pollen grains or spores, the number and shape of apertures, ornamentation, wall structure... and thus define the plant family, genus and, in the best case, species.

CIRAM laboratories, specialists in carbon-14 dating and archaeometric analysis.

CIRAM, a specialist in carbon-14 dating and archaeomaterials analysis, offers a meticulous examination of organic residues. To deliver relevant and accurate results, we interpret the results and remain at your disposal to discuss hypotheses according to your needs.

How is archaeological charcoal analyzed?

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Charcoal discovered during archaeological excavations is not used solely for carbon-14 dating. In fact, studying it also makes it possible to identify tree species, reconstruct ancient landscapes, and gain a better understanding of the practices of past societies. This discipline, known as anthracology, is based on the careful observation of the anatomical structures of charred wood.

Find out how laboratories analyze archaeological charcoal and what scientific information they can glean from simple charcoal fragments.

In summary:

  • Anthracology involves identifying wood species based on archaeological charcoal.
  • The samples are examined under a microscope along the three anatomical planes of the wood.
  • Scientists analyze numerous criteria to determine the origin of the wood, its condition before combustion, and its use.
  • These observations complement the carbon-14 dating results and enhance the interpretation of the remains.

How is an anthracological analysis conducted?

Anthracological analysis requires a meticulous sample preparation protocol. After smoothing the surfaces with a razor blade, the anatomical analysis of the charcoal samples is conducted along three axes: transverse, tangential, and radial. Through this three-dimensional observation, scientists can determine the family and genus, and, more rarely, the species.

Observations are made using a stereomicroscope (Olympus® SZ61 binocular loupe) and a dark-field metallographic microscope (Olympus® BX53M), under "natural" light (calibrated white light), coupled with digital cameras.

What anthracological criteria are analyzed?

Beyond identifying tree species, an anthracological study involves observing numerous anatomical characteristics. These observations make it possible to characterize the charcoal, reconstruct the history of the wood prior to combustion, and interpret archaeological contexts in greater detail.

These observations are not based solely on the anatomical identification of the wood species. Anthracologists also study various indicators that help trace the history of the wood before and during combustion.

Identify the origin and the part of the tree used

  • The presence of bark and pith: by observing both of these elements simultaneously in a sample, we can determine the stem’s size classification.
  • Reaction wood (typical of small branches or leaning trunks). This characteristic, combined with a pronounced curve, indicates that we are dealing with a small branch.
  • Calibration assessment: Analyzing the curvature of growth rings and the angle of wood rays will help identify the part of the tree from which the charcoal originated. Charcoal is classified into four categories:
Rings with steep curvatureIndicates very small-diameter logs
Dark circles with moderate curvature
Rings with low curvatureIndicates the use of large-diameter wood (large branches or trunks)
Rings with indeterminate curvatures

Determine the condition of the wood before burning it

  • The presence of tylles: Tylles form in the vessels of certain hardwood species during heartwood formation. The presence of tylles helps us identify potential tree species and also provides an indication of the sample’s location.
  • The presence of fungal hyphae: filaments can be observed in the vessels of the charcoal. They indicate the growth of fungi in the wood prior to combustion, particularly during the decomposition of a dead or dying tree. Observing them thus provides information about the condition of the wood before it was used.
  • Damage caused by insects or borers: Similarly, the presence of tunnels in the charcoal is evidence of an attack by insects or borers. It is possible to find charred remains of these organisms inside these tunnels. These clues prove that the wood was dead and worm-eaten before it was burned. In some cases, the sapwood of a living tree may be attacked by such organisms.

Analyze combustion conditions

  • The presence of radial shrinkage cracks and vitrification: Wood saturated with water will exhibit a large number of shrinkage cracks. Vitrification is a complex phenomenon that occurs during combustion. The characteristics of vitrification depend on the nature of the wood (species, size, moisture content) and the combustion conditions (temperature and oxygen supply). We distinguish four aspects of vitrification corresponding to four levels of carbonization:
Matte finish (level 0)The charcoal pieces have a matte appearance and are gray or black in color. Their anatomical structure is preserved.
Glossy finish (level 1) The coals range in color from dark gray to light gray and are very shiny.
Blended Look (Level 2)The surfaces are highly polished, and the anatomical structure is no longer discernible.
Scoriaceous appearance (level 3)This is the final stage of vitrification, in which the carbon structures are completely broken down.

Studying tree growth and its uses

  • The width of growth rings and growth rate. A narrow width indicates that the wood grew slowly (unfavorable growing conditions or an older tree). Conversely, wider rings indicate faster growth, associated, for example, with favorable environmental conditions or a younger tree. Consequently, the growth rate—that is, the consistency in ring widths—indicates whether the tree grew uniformly or whether there were events that temporarily hindered growth (climatic conditions, fungal attacks, injuries to the tree, etc.).
  • Signs of woodworking: Grooves or scratches on the surface may indicate that the wood was worked with tools.

Why are these observations important?

For each archaeological site included in the database, a systematic analysis of all charcoal samples is conducted according to the criteria mentioned above. The data, compiled in the form of tables and graphs, are then used to prepare an analysis report.

Anthracological analysis, therefore, involves more than simply identifying a type of wood. By observing the anatomical characteristics and alterations in the charcoal, specialists can determine the origin of the samples, the conditions under which the wood was burned, and the history of the wood used. This information enriches the archaeological interpretation and helps identify the most relevant samples prior to any carbon-14 dating.

To understand how anthracology improves the reliability of carbon-14 dating, see also our article on the role of anthracology in preventive excavations.

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You may have these questions about anthracology?

Why look at a piece of coal under a microscope rather than with the naked eye?

The anatomical structures that make it possible to identify a type of wood are invisible to the naked eye. Observation under a microscope reveals details such as vessels, wood rays, and punctures, which are essential for distinguishing between different types of wood.

Is it possible to analyze coal that is extremely degraded?

Yes, in some cases. Even when completely fragmented, charcoal pieces sometimes retain enough anatomical structures. However, extensive vitrification or advanced degradation can limit the possibilities for identification.

Does an anthracological analysis always make it possible to identify the species of wood?

No. Depending on the state of preservation of the charcoal and the observable anatomical characteristics, scientists most often identify the botanical genus, and more rarely the species. This is because certain tree species have very similar anatomical structures.

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In this article, we discuss the use of stable carbon and nitrogen isotopes (δ13C and δ15N) in bone collagen. Thanks to these methods, it is possible to identify the environment from which individuals have drawn their resources, as well as their relative positions in the food web. Stable isotope analysis not only reveals a group's food choices, but also socio-cultural and economic distinctions. Our laboratory scientists propose individual and collective dietary trends based on information from each individual.

Determining diet using stable carbon and nitrogen isotopes

Carbon-14 dating is not the only technique used in archaeometry. Stable isotope analysis of carbon and nitrogen also provides a wealth of information. As far as plants are concerned, our scientists distinguish between two types of photosynthesis:

  • In C3 for woody trees, rice, cotton or wheat which have a δ13C lower than -20 ‰ ;
  • In C4, such as grass, corn or sugarcane, which have a δ13C of between -10 and -20%.

We also use the isotopic ratio of nitrogen 15 and 14 to determine the origin of proteins.

Thanks to stable carbon and nitrogen isotopes, it is possible to determine the diet of a person or animal. We know, for example, whether they were carnivores, herbivores or omnivores. We can also determine whether the diet was more terrestrial or marine in origin.

Determining the state of preservation of the bone material, an important step in exploiting the samples

By quantifying carbon and nitrogen concentrations and analyzing the C/N ratio, it is possible to assess the state of preservation of the organic bone material, collagen. If collagen is in a poor state of preservation, the samples cannot be processed. Only a C/N in the 2.9 to 3.6 range will reveal a state of preservation compatible with reliable carbon-14 dating and isotopic study.

Interpretation of results

The results of carbon and nitrogen stable isotope analysis provide valuable information such as :

  • Origin of animal proteins (predominantly meat, milk/dairy products or fish);
  • Importance of cereals and legumes in ancient times.

It is also possible to compare results with different groups of individuals to detect different habits and to understand archaeological issues. Our scientists interpret the results and work with you to resolve your hypotheses.

CIRAM laboratories use a vario ISOTOPE select elemental analyzer (EA) from ELEMENTAR, which measures carbon and nitrogen concentrations (atomic %). This is a high-temperature combustion unit, up to 1200°C. The weighing range is from 20 µg to 300 mg. Concentration range is up to 7 mg absolute for carbon and up to 10 mg absolute for nitrogen. External accuracy (1s) is less than 0.1% for carbon and nitrogen. The elemental analyzer is the IRMS gas injection system. ELEMENTAR's IRMS isoprime precisION is an isotope ratio mass spectrometer that measures the stable isotope ratios of carbon (13C/12C) and nitrogen (15N/14N) expressed in per thousand (‰). External precision (1s) is 0.1 ‰ for δ13C and 0.15 ‰ for δ15N.

CIRAM, leader in dation and analysis since 2005

Stable isotope analysis is a goldmine for understanding the dietary and social habits of a group of individuals, but to be reliable it must be carried out on a significant corpus of individuals, otherwise the results cannot be representative.

CIRAM, laboratory dating and analysis since 2005, accompanies all its results with a complete, documented report. Our teams of researchers are always ready to listen to your needs and to work closely with you in the field.

Carbon-14 is a radioactive isotope present in all living organisms. This isotope can be used to date a large number of organic materials found in archaeological contexts.

Specialists in AMS carbon-14 dating, our scientists perform laboratory analysis of materials such as wood, bone and charcoal, as well as peat and other organic sediments. Discover our peat analysis methods for precise dating of all your organic residues.

Valuable information thanks to C14 peat analysis

Peat bogs, which have been present in some areas for over 10,000 years, provide valuable information on environmental changes such as climate and anthropological changes.

For example, it is important to be able to define chronologically the start of turfigenesis on an archaeological site in order to carry out a paleo-environmental reconstruction.

Thanks to the distribution of the dates obtained and their comparison with geomorphological, paleoecological and archaeological data, it is possible to trace the evolution and changes in landscapes and societies.

While radiocarbon dating is the most suitable method for the chronological setting of peat bogs and other sediments, there are several methodological problems.

Different types of peat

We can analyze and date many types of peat and organic sediments. For accurate results, we take care to eliminate macro-rests.

For silty peats that do not contain macro-rests, we use organic sediment.

Fibrous peat (the most common in the samples we analyze) is a mixture of decomposing plant remains and silty peat. For this type of peat, we extract the fibrous part, which undergoes ABA (acid-base-acid) treatment to eliminate carbonates and humic and fulmic acids.

Sediment and peat analysis methods

Methods differ between silty peats and fibrous peats.

Silty peat is first sieved to 100 microns to remove micro-rests. Silty peats and the insoluble fraction of humic sediments are treated exclusively with acid to remove carbonates.

Fibrous peats are first treated with acid, then alkaline and finally washed with acid to remove carbonates and humic acids.

It is also necessary to sieve the soluble fraction of humic sediments to remove macro-rests. Once the fraction is clean, we use a hot acid treatment, repeated if effervescence persists, followed by an alkaline treatment. Our scientists recover only the alkaline solution by centrifugation or filtration. Finally, an acid treatment is applied until precipitation.

As a general rule, the acid-washed and sieved organic sediment fraction will give a more accurate dating.

Results and calibration

Our scientists systematically calibrate the analyses using international standards. There is a difference between the gross age and the calibrated dates, depending on the data and the estimated age of the peat. Gross age is expressed in BP years, i.e. before 1950. We always convert raw ages into calibrated dates, which are corrected by the calibration curve.

CIRAM laboratories can help you interpret your results

CIRAM's laboratories are committed to delivering results that are in line with the realities of the field, and always provide a detailed commentary to address your specific issues. We are also at your service to provide additional information and discuss the results in order to advance your research and meet your needs in relation to the archaeological context.

Follow-up of results, dialogue between professionals and proximity, CIRAM laboratories deliver serious expertise in collaboration with you.

Isotopes are found everywhere in the environment, in plants via sediments and water, and in animal tissues (and therefore in human tissues) through eating, drinking and breathing. The analysis of stable isotopes, such as those of carbon, nitrogen, strontium, etc., makes it possible to study the diets of an individual or group of individuals, and to determine where an individual grew up or lived for the last twenty to twenty-five years of his or her life.

Strontium is abundant in nature, found mainly in rocks and sediments. As sediments are eroded and dispersed in water and food resources, it is absorbed by the body and incorporated into bone tissue. The isotopic ratio of strontium varies from one geographical region to another. Consequently, the analysis of strontium isotope ratios in bones or teeth can be used to determine the geographical origin of an individual, or to measure the homogeneity of a group of individuals.

Bone and teeth are the most frequently analyzed tissues, as they are hard and can be preserved for a long time in archaeological contexts. Bone is made up of two components: an organic matrix composed mainly of collagen, and an inorganic mineral matrix composed mainly of calcium phosphates. Bone is a living tissue that constantly renews itself as we grow and age. However, this process is very slow, and dense cortical bone reflects approximately the last ten to fifteen years of an individual's life. Teeth are also composed of organic and mineral materials, but tooth enamel does not renew itself. Teeth are therefore very useful in determining the environment of an individual's early years. Moreover, by comparing the teeth and bones of the same individual, it is possible to determine whether he or she has migrated from one region to another since childhood. Teeth show where a person lived during childhood, and bones show where they lived in the years leading up to death.

The principle is to compare the 87Sr/86Sr ratio of bone and/or dental enamel with that of the environment (sediments) around the archaeological site and in neighbouring regions (with different geological substrates). This will enable us to discuss the geographical origin of the food ingested by the individuals.

As far as possible, the selection of material should respect the preservation of the archaeological remains, while satisfying the needs of the study. Bone fragments should preferably be sampled from the cortical bone. To be relevant, the study should be carried out on series of several subjects, and we will always try to select the same anatomical part. For dental tissue studies, depending on the inter- or intra-individual study issues, we will either carry out an analysis per tooth, or a multi-analysis per stratum. Analysis will be carried out using a multi-collector mass spectrometer , with or without laser ablation.

Animal tooth samples are cleaned with ethanol and placed on a glass slide to remove the outer enamel surface. For the specific case of herbivore teeth, we will choose analysis zones at the base, middle and top of each tooth, in order to assess the enamel formed at different times in the individual's life. The spectrometer is coupled to a laser system, equipped with an ablation cell (LA-ICP-MS). For laser ablation analysis, 500 µm long line scans are applied, with a circular spot size of 100 µm and a translation speed of 5 µm/s. We use several internal reference materials of bioapatite, as well as apatite and carbonate.

Strontium analysis is invaluable for studying the movement of populations. Thanks to our experienced scientists and state-of-the-art equipment, strontium analysis is a specialty of CIRAM laboratories.

Carbon-14 dating is an essential method in archaeology. It can be used to determine the age of organic artifacts (wood, charcoal, bones, etc.).. When it comes to marine organisms, this method faces unique challenges due to the reservoir effect, a phenomenon that makes it difficult to interpret the results. In this article, we explain this concept, the correction methods used by scientists, and the limitations of C14 dating in marine environments.

The reservoir effect in C14 dating of marine organisms

Origins and mechanisms of the reservoir effect

The reservoir effect is a variation in carbon-14 (C14) concentration between terrestrial and marine organisms. This difference poses unique challenges for dating marine samples. Unlike atmospheric carbon, which is uniformly distributed and rapidly recycled, seawater has significantly lower C14 levels. This C14 deficit can be explained by several factors.

All First of all, carbon exchange between the atmosphere and the ocean is a slow process, due to the large mass of the oceans and the low solubility of carbon dioxide in water. In addition, ocean currents and the stratification of water masses result in a circulation of carbon that varies with depth and latitude. On the other hand, the ocean contains significant quantities of ancient carbon, particularly in the form of dissolved carbonate that has not been in recent contact with the atmosphere. This ancient carbon can have several origins, such as the dissolution of carbonate rocks or underwater volcanism, contributing to the apparent "aging" of marine organisms.

Consequences of the reservoir effect: the reservoir age

The consequences of the reservoir effect lead to "ageing aging The consequences of the reservoir effect lead to an "aging" of the age of marine organisms when they are carbon-14 dated. Marine organisms integrate less C14 than their terrestrial counterparts, due to the reduced levels of C14 in seawater. In fact, marine organisms start with a radiocarbon "clock" that is already out of sync with that of terrestrial organisms at the time of their death.

This difference, known as the "reservoir age", averages 400 years for surface ocean waters. However, reservoir age is not constant and can vary according to various geographical and environmental factors, such as water depth, proximity to freshwater sources, and the geochemical composition of water masses. For example, waters in estuaries or deltas show significant variations in carbon-14 concentrations due to mixing between fresh and marine waters, which impacts reservoir age. Similarly, C14 concentration varies according to latitude: polar waters often have higher reservoir ages due to slower circulation and low exchange with the atmosphere.

Scientists correct reservoir effect

Calibration methods with reference samples

Scientists rely on reference samples to compensate for shifts caused by the reservoir effect and thus obtain more accurate dating. One frequently used method is to compare results obtained on marine shells whose year of death is known. These shells from well-dated archaeological contexts or recent collections are used to calibrate the ages measured in C14. Using this reference point, researchers can adjust the results obtained for samples from the same region or of the same type, taking into account local variations in reservoir age.

Another key repository in this calibration process is the Marine 2020 Reservoir Database. This resource compiles data on reservoir ages observed around the world and provides corrective factors specific to different geographical locations. Scientists can then cross-reference the data from the sample under study with the information in this database, in order to apply an appropriate correction, taking into account the environmental and geographical particularities of the area concerned. This approach makes it possible to refine dating and reduce the margins of error associated with the reservoir effect.

Use of isotope ratio mass spectrometry (IRMS)

Isotope ratio mass spectrometry (IRMS) is an advanced technique used to analyze stable isotopes of carbon and nitrogen in samples. This technique is particularly useful for differentiating between sources of organic matter, identifying whether a sample comes from a terrestrial or marine environment. Isotope analysis therefore determines whether a correction for reservoir effect should be applied or not.

Using IRMS, archaeological dating laboratories can also refine the necessary corrections. For example, stable carbon isotopes can be used to detect the specific isotopic signatures of different carbon sources, such as those derived from marine or terrestrial photosynthesis. This process is essential for samples of uncertain origin, such as objects carved from organic materials of mixed or undetermined origin. Researchers can apply more precise corrections, reducing the uncertainties associated with the reservoir effect thanks to this improved knowledge of the isotopic composition of such samples.

Outlook for the reservoir effect

Geochemical models and reservoir age estimation

Another promising analytical method for improving age estimates of marine samples is the use of advanced geochemical models. These models integrate data on ocean circulation, atmospheric exchange, and spatial and temporal variations in ocean carbon-14 concentrations. These models can be used to calculate region-specific reservoir ages, adjusted for variables such as latitude, depth and ocean currents, taking into account the complex dynamics of oceanography. 

The use of geochemical models offers greater precision in estimating reservoir ages by modeling the physical and chemical processes that influence the distribution of carbon 14 in the oceans. These take into account elements such as carbonate dissolution, circulation of deep water masses and ocean-atmosphere interactions. Researchers obtain more reliable estimates of the age of marine samples by applying these models, even in complex environments such as estuaries and deltas.

Carbon-14 dating of marine organisms is a complex yet essential field in archaeology. It requires precise methods to correct for reservoir effects. While limitations remain, technological and methodological advances are continually improving the accuracy of these dates.

The scientists at CIRAM laboratories offer this type of analysis and are at your disposal to guide you through the dating process. If you would like to carry out a dating study, you can request a study to benefit from our expertise and obtain precise answers to your archaeological questions.

How to date bones using Carbon 14?

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6–8 minutes

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In summary:

  • Carbon-14 dating is the gold standard method for dating bones through collagen analysis.
  • When collagen is insufficient or degraded—particularly in the case of calcified bones—dating can be performed using bioapatite.
  • Dating bones also provides information about an individual’s diet through the analysis of stable isotopes.

Why is C14 used to date bones?

Carbon-14 dating, or radiocarbondating, is the dating method best known to the general public. It is, above all, the most effective technique for dating organic materials, particularly bones. Carbon-14 dating was developed in the 1940s and, like most dating methods, is based on radioactivity.

In living organisms, the amount of carbon remains stable. Carbon-14 is constantly decaying, but it is continually replenished through respiration or photosynthesis. This is why C-14 dating determines the time of death of an individual or plant, and the remaining amount of C-14 allows us to estimate the date of death.

Collagen extraction and dating

Why test for collagen?

Bones are very good chronological markers in an archaeological dig, as they are closely linked to the stratigraphy in which they are found. A bone is composed of a mineral part, bioapatite, and an organic part, collagen. Collagen is the most suitable fraction, and is normally used for radiocarbon dating.

Collagen Extraction

The preliminary step before dating will therefore be collagen extraction. To this end, the bones are treated with cold hydrochloric acid (HCl, 1 M) for 24 hours to remove any surface contamination and partially degrade the mineral portion of the bone, thereby making collagen extraction more effective. The samples are then treated with sodium hydroxide (0.1 M) at room temperature and treated once again with cold hydrochloric acid to prevent the absorption of atmospheric carbon dioxide. After washing with demineralized water, the scientists bring the samples to a boil to dissolve the collagen and then recover it.

Quality Control Before Dating

The collagen extracted in this way is incinerated at 920°C and converted into gas. During this step, an initial check of the C/N ratio is performed using an elemental analyzer (Elementar Vario ISOTOPE Select). This step is essential, as it serves as a quality control measure. Indeed, a C/N ratio between 2.9 and 3.6 indicates that the collagen is well-preserved and will yield a reliable date. If the C/N ratio falls outside this range, C-14 dating of the collagen will not be performed. In this case, the mineral portion of the bone must be used to date the bioapatite.

Next, stable isotopes of carbon and nitrogen will be analyzed by IRMS. These values will provide information on the diet of the individuals. At the same time, carbon dioxide from combustion is separated from other residues using a zeolite trap. This carbon dioxide is then catalytically converted into graphite using an automated system (AGE 3, Ion Plus).

C14 dating and calibration

In order to validate our analytical protocols, it is essential to first verify the accuracy of our measurements, as well as their reproducibility. To do this, we analyze international standards with known and recognized values. We use these values to assess our uncertainties, which are approximately 0.5 pMC and 0.1 to 0.2‰ for δ¹³C and δ¹⁵N. Real-time verification of the measured values for the standards allows us to identify and resolve any potential issues related to contamination, graphitization, and measurements.

Accelerator mass spectrometry (AMS) separates the different carbon isotopes. The 14C concentration is then determined by simultaneously comparing the measurements of 14C, 13C, and 12C with those of international standards (oxalic acid, standard CO2, and coal). We then calculate the conventional radiocarbon age using the method described by Stuiver and Polach, which accounts for isotopic fractionation correction.

The results are calibrated using OxCal v4.4 software. The measurement taken is expressed in two different ways: part of Modern Carbon (or pMC) and conventional age. Conventional age is expressed in years before 1950 (BP standing for before present), which is the reference year. Age is expressed to one standard deviation. The dating intervals reflect a two-sigma distribution, i.e. 95.4% of all solutions. The dated event can be found in any interval, regardless of the probability distribution, which is given for information only.

How can we date charred bones or bones with low collagen content?

Sometimes, certain bones no longer contain enough collagen to allow for reliable dating. This is particularly true of charred bones, but also of certain bones found in arid or acidic environments, where the protein has been severely degraded over time.

Before conducting any analysis, scientists assess the quality of the collagen based on the carbon-to-nitrogen (C/N) ratio. When this ratio falls between 2.9 and 3.6, the collagen is considered to be sufficiently well-preserved to be dated. However, if the ratio falls outside this range or if there is insufficient collagen, a different approach is required.

Bioapatite as an Alternative to Collagen

When collagen cannot be analyzed, dating is performed using bioapatite, which is the mineral component of bone. This method requires a specific preparation protocol to eliminate contaminants that could skew the results.

When it comes to calcined bones, laboratories prefer bones that have been completely bleached. These bones have generally been exposed to temperatures above 500 °C. At this stage of calcination, the structural carbonates in bioapatite are generally more resistant to chemical exchange with the soil, which improves the reliability of the dating.

After a purification step involving acid etching, the released carbon dioxide is recovered, purified, and then converted into graphite before being analyzed by accelerator mass spectrometry (AMS), following the same principle as for other samples dated using carbon-14.

Thanks to these specific protocols, it is possible to obtain reliable dates even when collagen is absent or severely degraded. This approach thus expands the possibilities for dating bone remains that would previously have been considered unusable.

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You might be wondering about these questions regarding the dating of bones?

Why might two bones found at the same site yield different ages?

Bones discovered in the same archaeological layer are not necessarily from the same period. They may have come from successive deposits or may have been displaced naturally or by human activity. Dating allows us to verify their chronological consistency with the excavation context.

Why date multiple bones from the same site?

Analyzing multiple artifacts helps confirm the chronology of a site. This allows us to identify any instances of reuse, stratigraphic disturbances, or distinct phases of occupation. This approach enhances the reliability of the archaeological interpretation.

How much bone is needed to perform a dating analysis?

Thanks to current accelerator mass spectrometry (AMS) techniques, a sample weighing anywhere from a few dozen to a few hundred milligrams may be sufficient, depending on the sample’s condition. The laboratory determines the minimum amount required before taking the sample.

Can a tooth be dated using carbon-14?

Yes. Teeth can be dated when their collagen is sufficiently preserved. As with bones, the laboratory first assesses the quality of the organic material before selecting the most appropriate analytical protocol. Teeth are often an excellent alternative when bones are too degraded.

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