Introduction

The etched and colored agate beads, as a daily decoration, religious decoration, or indicators of power and status for ancient people, were excavated in many ancient cultural locations such as Arabia, Persian Gulf, and Asia [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15]. Etched or stained beads were defined as a type of carnelian or chalcedony with a manufactured coloration pattern [1, 2, 4, 16]. In China, most etched or stained beads were unearthed from Xinjiang Uygur Autonomous Region, Tibet Autonomous Region, Yunnan Province, Guangdong Province, Henan Province, and Qinghai Province [17,18,19,20].

Previous studies decades ago [2, 3, 8, 21,22,23,24,25,26] have illustrated the shape, design, drilling technique, and color of the ancient beads. The beads chosen as ancient ornaments obviously underwent a series of different handicraft staining, which may indicate a symbolic and economic value. Previous studies have also found that the designed pattern changes over time and excavated regions, although there may be commercial activity conducted among the ancient civilizations at different locations [5, 10, 27,28,29,30]. Hence, excavated beads from different historical periods reflect craftsmanship advances and indicate craft skills development.

To a certain extent, the color styles of the ancient beads affect the appreciation of the people of the spreading destination through cultural infiltration. With the development of the urban society and technical expertise, natural pattern with simple surface polishing cannot express the motif of the elite communities [29]. The beads have changed dramatically during their spreading period, which covers the Neolithic Period around 7000 B.C. to the Early Historic Period [16, 29, 31]. One of the essential characteristics is the color, which can be correlated to the diverse line patterns of the beads. With the development of manufacturing, advances in agate beads-making technology resulted in new colors and various color patterns, such as white, red, and black [1, 4, 32, 33]. Pioneering works have divided colors of ancient beads into three color types: type I white-on-red, type II black-on-white, and type III black-on-red. Type I is the most common type, while black-on-white was less discovered. Type III was extremely rare. Artificial color patterns of the ancient beads can reflect the source area, production age, and handicraft development level. Differentiating the artificial origin color from natural color is the priority in the coloration research of the ancient beads. Therefore, interpreting the mineral character and the methods of manufacturing color is crucial for further research.

Agate mainly consists of microcrystalline quartz with a chemical composition of SiO2 and Mohs hardness of 6.5–7. Naturally produced agate can show various colors with waxy lustre, generally colorless or translucent due to the difference of various trace elements [34,35,36]. It is usually a difficult task to differentiate the manufactured color and idiochromatic color by optical observation. For the black-on-white type, it was considered that the beads were whitened entirely at the first step and then drawn with a metallic solution [4, 16, 37]. Human-controlled heat treatment plays a significant role in the red coloration manufacturing process [22]. Experimental research showed that the white line of type I comes from alkali solution etching [4, 16, 31, 37]. However, SiO2 was believed to have low reactivity. The terms etching, bleaching, and painting were used when describing the manufacturing mechanism of the white color [2, 4, 16, 38]. How do different mineral phases and colors respond differently to artificial staining? Illustrating the staining mechanism allows us to analyze humans’ manufacture and intellectual level at that time [22, 24, 30, 33].

Raman and FTIR spectroscopy are non-destructive and have been employed to identify mineral polymorphs and analyze mineral structure [17, 39,40,41,42,43,44]. The µXRF allowed us to in-situ identify the element composition of the mineral. SEM helps to investigate the coarseness of the beads' surface. Here, we studied eight ancient beads with different color types by µXRF, FTIR, Raman, and SEM techniques at a micrometer scale. The staining mechanism was revealed from a mineralogical perspective.

Experimental

Samples

The Jirzankal Cemetery, which is approximately 2500 years old, takes its name from the tableland on the eastern Pamir Plateau where it is located. Situated in SW Xinjiang, China, the cemetery shares borders with Tajikistan, Afghanistan, Pakistan, and India to the west, providing significant potential for western connections. During the extensive excavations carried out between 2013 and 2015, a range of exotic objects were discovered in the cemetery. For example, musical instruments such as harps found in burials M14 and M16 likely originated from the Near East, while silk fabrics discovered in burials M1 and M2 may have been transported from the eastern part of China [45]. Additionally, a variety of bone, glass, and agate beads discovered in the cemetery suggest broader connections with various cultures. Of these, 81 agate beads marked the cemetery as the largest bead-buried cemetery of its time in China. These beads exhibit various colors, both natural and artificial, and display intricate designs, providing valuable insights into the coloration of ancient agate beads.

This study focuses on eight agate beads excavated from burials BM11, BM14, BM23, and BM32, see Fig. 1. Among them, one bead is a plain red carnelian bead (H: BM23:12-7), four are etched carnelian beads with various white designs (A: BM32:7-6, E: BM14:9-1-8, F: BM23:12-1, G: BM11:22-2), and three are striped beads with pale and dark parallel layers (B: BM32:7-3, C: BM32:7-4, and D: BM11:22-1). These beads represent the major designs of agate beads found in China.

Fig. 1
figure 1

The eight ancient beads from Jirzankal cemetery, Xinjiang, NW China. (From left to right, BM32:7-6, BM32:7-3, BM32:7-4, BM11:22-1, BM14:9-1-8, BM23:12-1, BM11:22-2, and BM23:12-7 were labeled as A–H)

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Instrumentation and operating conditions

Raman spectroscopy was performed at room temperature using a Witec alpha300R confocal Raman microscope at the Institute of Geology and Geophysics, Chinese Academy of Sciences (IGGCAS). The laser beam was focused on the sample surface using a 50 × Zeiss microscope (NA = 0.75). The Raman data has been calibrated with a silicon peak of 520.7 cm−1. The spectra were collected with a 488 nm laser with a spectral acquisition time of 1 s and 60 accumulations for each measurement. The investigated spectra range from 100 to 4500 cm−1 using 300 grooves/mm optical grating. At least ten measurements were operated for one sample.

FTIR spectra were collected using a Bruker Vertex 70 V spectrometer at IGGCAS. A Hyperion 2000 IR microscope with an MCT detector cooled with liquid nitrogen connected to the Bruker Vertex 70 V spectrometer was used to obtain the microscopy IR spectra. Spectra were acquired from a single 100 × 100 μm spot on each analysed point. Background spectra were collected from a gold mirror. The FTIR spectra were recorded using reflectance mode with the co-addition of 64 scans between 650 and 4000 cm−1 at a resolution of 1 cm−1.

A Zeiss Gemini 450 electron microscope instrument at IGGCAS was used to study the morphology of the surface of the beads. The SE images were collected from the original surface. Samples for SEM measurement were not coated with carbon or any metal. The SE images were acquired at 2 kV accelerating voltage and beam current of 200 pA and working distance of 8.5 mm. The SEM was carried out under 3.01 × 10−6 mbar vacuum conditions.

MicroXRF experiments were performed on the Bruker M4 TORNADO plus µXRF spectrometer at IGGCAS, which enables the detection and analysis of the entire element range from carbon to americium. A dual silicon drift detector (30 mm2) measures X-rays with a resolution < 145 eV measured on Mn-Kα at a spatial resolution of∼20 µm [46]. In this study, all the scanning µXRF element mapping experiments were performed with an X-ray tube energy of 50 kV and a current of 600 µA, with 8 ms per pixel spectrum acquisition time and a pixel step-size of 18 µm. Data analyses, including obtaining elemental maps on all objects and quantitative XRF analysis from zone of interest, were undertaken with the characterization software provided by Bruker Micro Analytics.

Results and discussion

Optical appearance

Table. 1 shows the optical characteristics of the beads. Our visual observations of all the studied beads showed roughly faceted oval shapes with rounded edges. The most noticeable characteristic of the beads is the color and pattern. The dark red and black beads were transparent and showed a dull lustre, while the dark red and black beads were part translucent and showed a greasy lustre. The B and C beads feature a translucent zone located at the head of the beads(yellow rectangle schematic in Figs. 1, 2). Of all the color types, the white-on-red variety was the most common. According to Beck's division of the prevailing era of the beads type, their pattern characteristics show the producing age of approximately 2300 years, which is consistent with the dating results of the cemetery [2, 12, 14, 47, 48]. The carnelian beads E, F, G, and H were translucent and showed a vitreous lustre. They varied from white (‘scattered white’ or ‘idiochromatic white’, see Fig. 1 and Section “Idiochromatic white and scattered white”) to light red to dark red to black (Table 1).

Table 1 Optical characteristics of the eight studied beads
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Fig. 2
figure 2

a, c, d: Optical graph shows the pit of the scattered white zone, b Optical graph shows the cavity and the white layers were cut by the edge of the black zone

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Figure 2 shows that the scattered white zones of samples A, B, and G are pits. The light red, the dark red, the black, and the idiochromatic white zones are flat and smooth compared with the scattered white zone. The scattered white line covers the flat surface with a distance range from approximately 0.5 mm (Sample G) to 6.0 mm (Sample B). The idiochromatic white gel layers and the cavity of the sample D are seen without artificial alteration [49, 50]. The extension trend of the white layers with different degrees of whiteness was cut by the edge of the black zone (Fig. 2-b).

µXRF

All samples contained Si, O, Na, K, Ca, and Fe. Si and O account for 98wt.% of the elements in weight percent (Table 2), indicative of the chemical composition of the α-quartz mineral [51]. The scattered white zone contains significantly more Na and Ca than other color zones. This artificial staining process must have used some Na-containing and Ca-containing liquid—for example, plants and calcium carbonate minerals. K is evenly distributed across samples at a lower content. Based on the µXRF data (Table. 2) and optical microscope observation (Figs. 1,2), Fe is uniformly distributed in samples A and B, while the Fe measured by the other four carnelians (E, F, G, and H) show irregular distribution on its surface. Therefore, higher Fe content (0.04%) was observed (Table 2).

Table 2 Chemical compositions of the different color zones
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Raman spectra

All beads exhibited the characteristic Raman peaks of α-quartz at 464 cm−1 and weak peaks at 128 and 207 cm−1. The 464 cm−1 is the strongest Raman peak assigned to the vibration of the SiO4 six-membered ring, and the 128 and 207 cm−1 peaks were assigned to Si-O-Si bending vibrations of α-quartz microcrystalline [52]. The shoulder at 502 cm−1 corresponds to symmetric stretching vibrations of the four-membered Si-O-Si ring, which was proved to be moganite by previous Raman studies [52,53,54,55]. All the Raman spectra in Fig. 3 and the spectra of the idiochromatic white zone of B-b, C, and D (Fig. 4) confirmed the presence of moganite. This indicates that the moganite and microcrystalline quartz coexists in the original agate stone materials of beads. According to the integral ratio of the 502 cm−1 and 465 cm−1 bands [56], the moganite content of all the studied samples is in the range 0 to 50wt%.

Fig. 3
figure 3

Raman spectra of A dark red zone, B black zone, C dark red zone, D black zone, E red zone, F red zone, G red zone, and H red zone

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Fig. 4
figure 4

Raman spectra of A scattered white zone, B-a scattered white zone, B-b part translucent zone, C-a idiochromatic white zone, C-b part translucent zone, D idiochromatic white zone, E scattered white zone, F scattered white zone, and G scattered white zone

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The distinct Raman peaks demonstrate that the black zone of samples A and D is formed due to artificial alteration without breaking the main chemical bond (Figs. 2, 3, 4). Also, two relatively strong bands were distinctly observed at 1380 and 1580 cm−1, which are absent in the spectra of most of the red and white zones. These features can be interpreted as the D and the G peaks of disordered carbon [57, 58]. The minor carbon content could account for the dark red and black color of A and D samples, respectively. For the spectra of the white zone, no carbon was detected except sample B.

In the part translucent zones of B and C (Dashed rectangle symbol shown in Figs. 1, 2), the intensity of the Raman peaks is much stronger than any other zone (Fig. 4), indicating a low-defect quartz structure with less intercrystalline porosity [56]. As a result, a zone with a higher crystallinity degree could accommodate less exotic elements. This indicates that the crystallinity degree of the translucent zones is much greater, which in turn prevents the staining process.

Selected Raman spectra collected from the scattered white zone of the beads are shown in Fig. 4. It can be seen that the moganite peak is absent. However, the moganite peak was still observed from spectra collected from the idiochromatic white zone of samples C and D.

Raman spectra of the irregularly distributed red dots at the surface of the sample E (Fig. 5) confirmed the presence of hematite, with peaks centered at 229, 299, and 409 cm−1 [59, 60].

Fig. 5
figure 5

Raman spectra of the red dot of sample E

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FTIR spectra

The red, the dark red, the black, the idiochromatic white and the part translucent zones of all of the samples show similar FTIR patterns with two prominent absorption bands at ~ 1097 and ~ 1187 cm−1 and two weak absorption bands at 798 and 778 cm−1 (Figs. 6, 7), which can be assigned to the asymmetric stretching vibration of Si-O and symmetric stretching vibration of Si-O-Si, respectively [44, 60,61,62]. FTIR bands indicate that the mineral composition of the red and black zones are characteristic of agate and contain a low amount of moganite (Fig. 6) [63]. The band ratio of 1097 cm−1 peak and the trough at 1158 cm−1 is sensitive to the abundance of moganite [56]. However, this parameter only works well for high moganite content samples (more than 50%) [56].

Fig. 6
figure 6

FTIR spectra of A dark red zone, B black zone, C dark red zone, D black zone, E red zone, F red zone, G red zone, and H red zone

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Fig. 7
figure 7

FTIR spectra of A scattered white zone, B-a scattered white zone, E scattered white zone, F scattered white zone, G scattered white zone, C-a idiochromatic white zone, B-b part translucent zone, C-b part translucent zone, and D idiochromatic white zone

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For the scattered white zone, the two prominent peaks show a redshift to the low wavenumber region. A sharp absorption band is observed at ~ 1084 cm−1, and a subtle band at 1180 cm−1. These bands are expected to be mainly associated with Si-O stretching vibrations of α-quartz [64]. Moganite was considered to be an unstable precursor mineral of α-quartz in previous studies [44, 65,66,67], and there may be a tendency for a slow transition to quartz in natural environments. This is why moganite is easier to be etched at high temperatures. Unlike samples A, B-a, E, and G, the FTIR of the scattered white zone of F, the 1097 cm−1 peak remains unchanged while the 1187 cm−1 peak redshifts (Fig. 7) to 1180 cm−1. This is proposed to be attributed to the grinding and polishing process after etching. The etched pit on F bead was eliminated by grinding, resulting in a slight redshift.

SEM

The SEM images reveal that most of the observed surfaces are flat, which means the beads had been produced by a grinding and polishing process (Fig. 8) [22, 23]. Figure 8i, j show the interface zone between the scattered white and the dark red zones with different magnifications. The scattered white zones always have coarse corrosion surfaces (Fig. 8f and j) compared with the red, the black, and the idiochromatic white zone. Scattered white zones are often lower in elevation than red zones (Fig. 8 i, j). This indicates that the white color was artificially added after polishing. The etching process weakened the glaze slightly, which may result in a scattered white color. Furthermore, the chemical structure of the agate beads was partially damaged, resulting in a formation of the diffuse reflection surface (Fig. 9).

Fig. 8
figure 8

SEM image of (a) red black zone of D, (b) white zone of D, (c) black zone of B, (d) translucent zone zone of B, (e) white zone of B, (f) white zone of B, (g) dark red zone of C, (h) white zone of C, (i) bottom right show the red and left upper zone show the scattered white zone of A, (j) the inserted rectangle zone of A in (i) with higher magnification

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Fig. 9
figure 9

Schematic drawing of etching process observed in side view of the agate surface

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Discussion

Red and dark red

Beads in this study can be divided into four color categories based on their character and staining mechanism. The first is red, the most common color of the excavated beads.

Natural occurring chalcedonies have different colors and intercrystalline porosities generated by the minor elements and mineral proportions [52, 54]. However, intentional heat treatment of natural agate produces the desired lustre, flaking properties, and the most significant result, red color [22, 33]. Since the structure of natural agate is not compact, the color of agate can be altered by exotic element infiltration into the micropores or subtle channels. Then the iron element in the pores is oxidized to ferric iron to form hematite after heat treatment, supporting the Raman data in this study together with previous literature [68, 69]. Hence, ferric iron is often uniformly present throughout the mineral pores and channels, causing the red color known as carnelian red. In some places with high concentrations, red dots found on the surface of the carnelian indicate the presence of hematite (Fig. 5). The irregular distribution of Fe on the surface of carnelian is caused by the oxidation of the Fe nuclei during the heating process in the bead manufacture or exogenous pollution during burial [6, 60]. Generally, this results in a color change throughout the particle. Therefore, carnelian is the most common material for bead making and is made into various shapes.

The evenly distributed Fe in A may be the source of its dark red color, indicating that these beads may not have undergone a heating process in the air, but are original Fe cations come from the infiltration of a specific iron-containing liquid. Fe and Mn cations are usually the color-forming elements of natural agate [69,70,71,72]. The Fe cations penetrated the surface and spread out across the entire beads.

Although quartz has better crystallinity, it is unsuitable for staining due to its lack of channels. For zone with high crystallinity, the degree of staining will be significantly lower due to the compact crystal structure and smaller pores. This is the formation characteristics of the infiltration-induced red color.

Black

Black-colored agate can form naturally by introducing carbon-bearing material into the porous silica matrix [35]. Continuous black bands can be observed alternating with the white bands, indicating that the black bands were formed successively after or before the white band [73]. Similar to the natural black agate, artificial black-colored beads come from disseminated carbonaceous matter [29, 36, 60, 74]. However, black-colored beads usually appear in a regularly distributed black banded or overall black color type rather than alternating bands, regardless of their natural color bands. The transition boundary between the studied beads' black and white sections clearly cut the agate's concentric zoning bands.

The lack of a line pattern means that the methodology of making the black beads differs from the scattered white beads. This process may be performed by immersing the beads in some kind of liquid. In the iron age, diverse kinds of food, such as honey or sugar, could serve as the carbon source [31]. The black staining process was most probably realized by the organic carbon penetration through the subtle channels in the agate [31, 36]. Because of the principle of penetration, the translucent part of the beads has a slightly different consistency and porosity.

Idiochromatic white and scattered white

Both idiochromatic and scattered white colors appear as common color types of the excavated beads. However, the bead craftsman did not use the same strategies to make idiochromatic white and scattered white beads. The idiochromatic white color comes from the mineral composition that was originally possessed after the quartz formation (Fig. 1, samples C and D). Researchers have found that carnelian beads with a scattered white pattern are clearly due to artificial processing technology rather than an idiochromatic white [1,2,3, 16, 21, 75]. Some studies have proposed that the scattered white color was generated by the ‘micro fractures’ of the carnelian surface [8, 31]. Potash and washing soda were believed as an adhesive material for the white carnelian [4, 16, 75]. Some scholars advocate using’bleaching’ since they proposed that the beads are not actually etched but only in a way of white color painting on the red carnelians [1, 38]. According to the μXRF (Table. 2), Raman (Figs. 3, 4), FTIR (Figs. 6, 7), and SEM (Fig. 8) data, we conclude that it is etched into red rather than painted with paint [38, 68]. The pores on the surface of the white zone of agate are irregularly distributed, indicating a corrosion surface. The incident light was scattered by the etched coarse surface of the carnelian, resulting in a white-looking and opaque color.

Generally speaking, the main components of the unearthed beads are α-quartz and moganite. However, the Raman spectrum shows no evidence of moganite peaks in the white zones (Fig. 4). This suggests that the formation of the white color is related to the reaction of moganite. Moganite belongs to the monoclinic crystal system and is generally considered to be an intermediate phase in the transformation of amorphous SiO2 to crystalline α-quartz [54, 65, 66, 76]. It contains a large number of structural defects in the form of Si-OH, which has greater reactivity than the Si-O bond in α-quartz [77, 78]. Therefore, the chemical reaction should occur first in Si-OH rather than Si-O, although we cannot rule out the reaction of the Si-O bond. Alkali-silica reaction reactions can occur in quartz-bearing rocks [79]. Kirar plant juice was used when producing etched beads without water [4]. However, the washing-soda was proposed to be the active ingredient of the etching liquid rather than the kirar plant juice based on the results of this study [68]. Therefore, moganite is likely to be etched by the following reaction equation (Fig. 9):

$${\text{Na}}_{{2}} {\text{CO}}_{{3}} + {\text{ SiO}}_{{2}} \, \triangleq \,{\text{Na}}_{{2}} {\text{SiO}}_{{3}} + {\text{ CO}}_{{2}}\uparrow$$
(1)
$${\text{Na}}_{{2}} {\text{CO}}_{{3}} + {\text{ Si}}\left( {{\text{OH}}} \right)_{{4}} = {\text{ Na}}_{{2}} {\text{SiO}}_{{3}} + {\text{ CO}}_{{2}}\uparrow + {\text{ 2H}}_{{2}} {\text{O}}$$
(2)

Therefore, our analysis considers that etching is more suitable and accurate for this kind of bead because the moganite was removed by chemical reactivity. Etching rather than bleaching was proposed to be used to accurately describe the carnelian beads because the moganite was removed by chemical reactivity.

In addition to Na, small amounts of K have been detected in μXRF, Na and K can come from etching liquid, and K may also come from plant ash which was made by burning the Amaranth species plant [31] or kirar tree [80]. For the prehistoric period, carbonate stone could serve as a Ca source by heating (Eq. 3). Therefore, relatively high levels of the element Ca are likely derived from the CaCO3 in the etching liquid. It may have undergone the following reaction process (Fig. 9):

$${\text{CaCO}}_{{3}} \triangleq {\text{CaO }} + {\text{ CO}}_{{2}}\uparrow$$
(3)
$${\text{CaO }} + {\text{ H}}_{{2}} {\text{O }} = {\text{ Ca}}\left( {{\text{OH}}} \right)_{{2}}$$
(4)
$${\text{CaO }} + {\text{ SiO}}_{{2}} \, \triangleq \,{\text{CaSiO}}_{{3}}$$
(5)
$${\text{CaO }} + {\text{ Si}}\left( {{\text{OH}}} \right)_{{4}} = {\text{ CaSiO}}_{{3}} + {\text{ 2H}}_{{2}} {\text{O}}$$
(6)
$${\text{Ca}}\left( {{\text{OH}}} \right)_{{2}} + {\text{ SiO}}_{{2}} = {\text{ CaSiO}}_{{3}} + {\text{ H}}_{{2}} {\text{O}}$$
(7)
$${\text{Ca}}\left( {{\text{OH}}} \right)_{{2}} + {\text{ Si}}\left( {{\text{OH}}} \right)_{{4}} = {\text{ CaSiO}}_{{3}} + {\text{ 3H}}_{{2}} {\text{O}}$$
(8)

In the presence of calcium hydroxide and sodium carbonate, the following reactions may also produce sodium hydroxide (Fig. 9):

$${\text{Ca}}\left( {{\text{OH}}} \right)_{{2}} + {\text{ Na}}_{{2}} {\text{CO}}_{{3}} = {\text{ CaCO}}_{{3}} + {\text{ 2NaOH}}$$
(9)
$${\text{2NaOH }} + {\text{ SiO}}_{{2}} = {\text{ Na}}_{{2}} {\text{SiO}}_{{3}} + {\text{ H}}_{{2}} {\text{O}}$$
(10)
$${\text{2NaOH }} + {\text{ Si}}\left( {{\text{OH}}} \right)_{{4}} = {\text{ Na}}_{{2}} {\text{SiO}}_{{3}} + {\text{ 3H}}_{{2}} {\text{O}}$$
(11)

Regardless of the reaction pathway, the etching process is accomplished by breaking Si-O-Si or Si-OH of the moganite to form soluble silicate and carbon dioxide (Fig. 9). According to these results, moganite should be more reactive than α-quartz. In this sense, the temperature will affect the etching rate depending on the moganite proportion and different Si-OH content [51, 54, 81, 82]. Forming a corrosion surface with different depths eventually (Fig. 8f, i, j). A white color can be observed since the rough surface scatters incident light of different wavelengths in all directions.

Conclusions

The identification of the artificial staining mechanisms used on ancient agate beads has been investigated using μXRF, Raman, and FTIR techniques. In this study, systematic mineralogical analyses were conducted on carnelian beads from an Iron Age cemetery on the Pamir Plateau and, for the first time, revealed the different coloration mechanisms of red, black, and white.

In unstained beads, Raman spectroscopic studies revealed a characteristic peak at 502 cm−1, confirming the presence of moganite. All ancient beads with varying colors exhibited similar FTIR features, with variations in peak intensity. The position of the of the 1097 and 1187 cm−1 doublet shifted to 1084 and 1180 cm−1 with decreasing amounts of moganite. The white zones of samples A, B, E, and G were absent of moganite, which was confirmed by the FTIR data as two prominent peaks that shifted to the low-frequency region compared to the red zone. Higher amounts of Ca and Na were detected using μXRF analyses for the scattered white zone compared to other zones, indicating the etching mechanism of the scattered white color.

Through the application of heating, organic matter infiltration, and alkali etching techniques, beads could be regenerated with a novel appearance to cater to the varied preferences of people from different regions. The red color was produced from a heat treatment, while the black color came from carbonaceous matter infiltration. The scattered white appearance was assigned to the rough and irregular coarse mineral surface that reflected light, resulting from the chemical etching process.

In conclusion, samples C and D belonged to the black-on-idiochromatic white type. The black zones of B and D were manufactured through carbon infiltration, while the white-on-red type samples E, F, G, and H had undergone heat treatment that enhanced the red color and drove the etching reactivity.

The mineralogical study presented in this article is significant for analyzing the geographical spread of agate beads and studying ancient handicrafts. The unique mineral composition and excellent craftsmanship of these colorful ancient beads illustrate a developed pre-historic chemical technology. Further studies may be necessary to better understand the innovation and spread of the color styles and how they might have changed over time.