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This paper provides a detailed technological characterization of the Roman opus sectile glasses (second century AD) coming from the renowned Gorga collection. Nine glass samples corresponding to imitations of the porfido verde antico, cipollino rosso, rosso antico, giallo antico, diaspro nero e giallo, semesanto and agate/alabaster stones were studied. The aim of this study was twofold: (i) archaeometric, i.e., to provide valuable data on the production, raw materials and techniques of these refined Roman glasses that mimic precious stones and (ii) methodological, i.e., to highlight the good performance of combining polished thin sections and local probe measurements for the study of glassy microstructures. Based on the nature of the flux used, the glasses from the samples were classified as either natron-type or mixed-type (natron/plant ash). The latter stem from remelted glasses and contain relict grains of wollastonite that were not found in the pure natron samples. Relict wollastonite crystals appear to be a proficient petrographic marker to spot recycled glasses along with the commonly used chemical fingerprints. Different production and colouring techniques were identified, even for a given type of imitated stone. Metallic Cu, Ca antimonates and Pb-Fe antimonates were the three opacifiers used for the opaque glasses. Based on the crystal morphologies, metallic Cu and Ca antimoniates were possibly synthesized in situ simultaneously with the glass, whilst the Pb-Fe antimonates were prepared ex situ. The working temperatures for these glasses were estimated within the 900–1100 °C range based on the presence and known thermal stability of some identified crystal phases. [ABSTRACT FROM AUTHOR]

Owing to the high market values of natural sunstones in Oregon, a kind of artificially diffused red feldspar exhibited at the Tucson Exhibition at the beginning of this century, whose color origin is the same as that of natural sunstone (copper nanoparticles). However, the details of the artificial diffusion process are less disclosed, there is no systematic method to obtain such gemstones. In this paper, we developed the high-temperature copper diffusion process for the surface recoloring of faceted labradorites, which are partly buried in the diffusant. By optimizing the experimental parameters of high-temperature copper diffusion, we successfully recolored the faceted labradorites to red and light red. The gemological and spectroscopic characteristics of the recolored faceted labradorite were further characterized. The red and light-red faceted labradorites exhibited the unique surface plasmon resonance absorption peaks of copper nanoparticles near 580 nm, which is the origin of red color. The typical inclusions formed in the faceted labradorite is in the shape of "fire cloud". The interface of red and light-red faceted labradorite that is in contact with the diffusant is less contaminated, we believe that the contamination could be further reduced or eliminated by optimizing the high-temperature copper diffusion process. The way that the sample is in contact with the diffusant partly is versatile and promising in the surface treatment of materials that have already been processed. [ABSTRACT FROM AUTHOR]

Featuring subtle lithological alterations in the host rocks and containing colossal gemstone crystals, the scheelite deposit at Xuebaoding in the Pingwu region of Sichuan Province exhibits characteristics typical of a vein-like hydrothermal-type deposit. The scheelite from the Xuebaoding region is renowned for its high saturation of color, perfect crystal shape, and pure color. In this study, its crystal structure and mineralogical, geochemical, and in situ Sr-Nd isotope characteristics are all systematically characterized. Our objective is to determine the source of ore-forming materials, the timing of the mineralization, and the chemical composition of scheelite, including major elements, trace elements, and rare earths elements (REE). The scheelite samples were analyzed with a variety of methods such as polarizing microscopy, X-ray powder diffraction (XRD), X-ray fluorescence spectrometry (XRF), electron probing, and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). In addition, conventional gemological tests were performed using instruments including gemstone microscopes, GI-UVB ultraviolet fluorescent lamps, grating spectroscopy, etc. The results demonstrate that scheelite exhibits a high refractive index, excellent crystallinity, and a granular structure. Clear color bands and ring structures are observed within the minerals, accompanied by interference colors of light blue, blue, and yellow. Additionally, the mineral components are relatively concentrated, with muscovite and illite serving as accessory minerals. Furthermore, the chemical composition of scheelite reveals a WO3/CaO mass ratio that approaches or exceeds the ideal value. Moreover, it exhibits a wide range of variations in total rare earth element (∑REE) content, which is characterized by an enrichment of light rare earths (LREE), significant negative Eu anomalies, and insignificant Ce anomalies. In addition, the metallogenic formation of scheelite can be estimated to have occurred during the Toarcian stage in the Lower Jurassic Epoch period, approximately 183 Ma. The study further revealed that A-type granite serves as the genesis type of scheelite, with most of the ore-forming materials originating from the upper crust and a few derived from younger crustal sources. [ABSTRACT FROM AUTHOR]

The Jizerka Quaternary alluvial placer in the Czech Republic has been a well-known source of gemstones since the 16th century, and the only one in Europe that has yielded a significant amount of jewel-quality sapphire. Besides Mg-rich ilmenite ("iserine"), which is the most common heavy mineral at the locality, some other minerals have been mined for jewellery purposes. These are corundum (sapphire and ruby varieties), zircon ("hyacinth" gemstone variety) and spinel. Here, we present a detailed petrological and geochronological investigation of the enigmatic relationship between the sapphires and their supposed host rocks, supporting their xenogenetic link. Our hypothesis is based on thermal resetting of the U–Pb isotopic age of the zircon inclusion found inside Jizerka blue sapphire to the estimated time of the anticipated host alkaline basalt intrusion. The host rocks of the gemstones (sapphire and zircon) and Mg-rich ilmenite are not yet known, but could be related to the Cenozoic volcanism located near the Jizerka gem placer (Bukovec diatreme volcano, Pytlácká jáma Pit diatreme and Hruškovy skály basalt pipe). The transport of sapphire, zircon and Mg-rich ilmenite to the surface was connected with serial volcanic events, likely the fast ascent of alkali basalts and formation of multi-explosive diatreme maar structures with later deposition of volcanoclastic material in eluvial and alluvial sediments in nearby areas. All mineral xenocrysts usually show traces of magmatic corrosion textures, indicating disequilibrium with the transporting alkali basalt magma. In order to constrain the provenance and age of the Jizerka placer heavy mineral assemblage, zircon inclusion and associated phases (niobian rutile, baddeleyite and silicate melts) in the blue sapphire have been studied using LA–ICP–MS (laser ablation–inductively coupled plasma–mass spectrometry) geochemistry and U–Pb in situ dating. Modification of the zircon inclusion into baddeleyite by exposure to temperature above 1400 °C in a basaltic melt is accompanied by zircon U–Pb age resetting. A zircon inclusion in a Jizerka sapphire was dated at 31.2 ± 0.4 Ma, and its baddeleyite rim at 31 ± 16 Ma. The composition of the melt inclusions in sapphire and incorporated niobian rutile suggests that the parental rock of the sapphire was alkali syenite. The Eocene to late Miocene (Messinian) ages of Jizerka zircon are new findings within the Eger Graben structure, as well as among the other sapphire–zircon occurrences within the European Variscides. Jizerka blue sapphire mineral inclusions indicate a provenience of this gemstone mineral assemblage from different parental rocks of unknown age and unknown levels of the upper crust or lithospheric mantle. [ABSTRACT FROM AUTHOR]

Absorption spectroscopy has been widely used in gemstone societies as it enables the identification of the origin and post-treatment of gemstones in a non-destructive way. The infrared (IR) range is critical for studies of gemstones such as corundum, emerald, and diamond. Regarding the corundum sample, absorption peaks related to the -OH bond could be used as an index for heat-treatment detection, and different types of inclusions could be identified by analyzing the IR absorption spectrum. The most widely used method for measuring IR absorptions is Fourier-transform infrared spectroscopy (FTIR), which was designed based on the working of the Michelson interferometer. However, FTIR has a few limitations, such as a long measurement time and difficulty in sample placement, which limits its full automation capability. In this study, a mid-infrared (MIR) spectrometer relying on the upconversion phenomenon of non-linear crystals was used to measure the absorption spectra. Corundum with heat treatment features and/or with different common types of inclusions were measured by both transmission and reflection modes. After comparison with the FTIR spectra captured on the same sample set, the same target peaks could be captured with a shorter measurement time and easier operation. The developed MIR spectrometer could directly measure the absorption spectrum in the 2–4.5 µm (2200–5000 cm−1) range within a few seconds. Meanwhile, as both transmission and reflection modes were available, both loose and mounted gemstones could be measured, supporting the widespread use of this device in large-scale production and its ability to achieve full automation. [ABSTRACT FROM AUTHOR]

Isomorphic substitutions of extra-framework components in sodalite-group aluminosilicate minerals and their thermal conversions have been investigated using infrared, Raman, electron spin resonance (ESR), as well as ultraviolet, visible and near infrared (UV–Vis–near IR) absorption spectroscopy methods and involving chemical and X-ray diffraction data. Sodalite-related minerals from gem lazurite deposits (haüyne, lazurite, and slyudyankaite) are characterized by wide variations in S-bearing extra-framework components including SO42− and various polysulfide groups (S2●−, S3●−, S4●− radical anions, and S4 and S6 neutral molecules) as well as the presence of CO2 molecules. Heating at 700 °C under reducing conditions results in the transformation of initial S-bearing groups SO42− and S3●− to a mixture of S2−, HS−, S2●−, and S4●− and transformation of CO2 to a mixture of CO32− and C2O42− or HC2O4− anionic groups. Further heating at 800 °C in air results in the decomposition of carbonate and oxalate groups, restoration of the SO42− and S3●− groups, and a sharp transformation of the framework. The HS− anion is stable only under reducing conditions, whereas the S3●− radical anion is the most stable polysulfide group. The HS−-dominant sodalite-group mineral sapozhnikovite forms a wide solid-solution series with sodalite. The conditions required for the formation of HS−- and CO20-bearing sodalite-group minerals are discussed. [ABSTRACT FROM AUTHOR]

In this study, we report the experimental findings of a multi-methodological and comparative investigation of a natural (from the Wah Wah Mountains of Beaver County, Utah) and three synthetic (hydrothermally grown) gem-quality red beryls by means of: gemmological standard testing, laser ablation inductively coupled mass spectroscopy, infrared and Raman spectroscopy, ultraviolet–visible–near infrared absorption spectroscopy, and single-crystal X-ray diffraction. Gemmological, crystallo-chemical, and spectroscopic features of the natural and synthetic stones enabled us to unveil the causes of their color (from red, to purplish-red, or orange-red) and how different and complementary techniques can be efficiently used to discriminate between natural and synthetic materials, based on non-destructive, micro-destructive, and destructive techniques. [ABSTRACT FROM AUTHOR]

Ruby (red corundum) is one of the most prominent colored gemstones in the world. The highest-quality ruby ("pigeon blood" ruby) comes from marbles of the Mogok Stone Tract in central Myanmar. Although Mogok ruby has been exploited since the 6th century AD, the formation time of this gemstone is ambiguous and controversial. In this paper, we describe a mineralogical, geochemical, and geochronological study of ruby and titanite in ruby-bearing marbles obtained from an outcrop in the Mogok Stone Tract, central Myanmar. Petrographic observations have shown that titanite generally occurs in the marble matrix or occurs as inclusions in ruby. These two types of titanite exhibit identical chemical compositions. In situ secondary ion mass spectrometer (SIMS) U–Pb dating of the separated titanite from two representative samples of ruby-bearing marbles yielded lower intercept ages of 25.15 ± 0.24 Ma (MSWD = 0.26) and 25.06 ± 0.22 Ma (MSWD = 0.15), respectively. Because the closure temperature of the U–Pb system in titanite is close to the temperature of ruby growth, the obtained U–Pb ages (~25 Ma) are suggested to represent the timing of the studied ruby formation in Mogok. The acquired ages are in agreement with the timing of post-collisional extension in the Himalaya related to the migration of the eastern Himalayan syntaxis. Combining our dating results with previous geochronological data from the Mogok Stone Tract, we suggest that the formation of the studied ruby is most likely related to the high-temperature metamorphic event in the marbles during the India–Asia collision. Our study not only confirms that texturally constrained titanite could be a precise geochronometer to date the mineralization of different types of ruby, but also provides important geochronological information linking gemstone formation to the India–Asia collision. [ABSTRACT FROM AUTHOR]

Growing public interest in getting information on the origin of raw materials used to manufacture goods for daily life has triggered the development of concepts to increase the transparency of raw material supply chains. Analytical proofs of origin (APOs) for raw materials may support those transparency concepts by giving evidence about the origin of a specific raw material shipment. For a variety of raw materials like gemstones, TTT (tantalum, tin, tungsten) minerals, and others, APOs have been developed. The identification of features that distinguish different origins, databases of those features from reliable reference samples, and a data evaluation strategy adopted to the envisaged application scenario are the key aspects of APO methods. Here, an overview is given on APO methods developed for different raw materials and application cases. [ABSTRACT FROM AUTHOR]

Five samples of differently colored sodalite-group minerals from gem lazurite deposits were studied by means of electron microprobe and wet chemical analyses, infrared, Raman, electron spin resonance (ESR) and UV-Visible spectroscopy, and X-ray diffraction. Various extra-framework components (SO42−, S2− and Cl− anions, S3•−, S2•− and SO3•− radical anions, H2O, CO2, COS, cis- as well as trans- or gauche-S4 neutral molecules have been identified. It is shown that S3•− and S4 are the main blue and purple chromophores, respectively, whereas the S2•− yellow chromophore and SO3•− blue chromophore play a subordinate role. X-ray diffraction patterns of all samples of sodalite-group minerals from lazurite deposits studied in this work contain superstructure reflections which indicate different kinds of incommensurate modulation of the structures. [ABSTRACT FROM AUTHOR]

Indicator minerals (IM) have been used in the research of gemstone and base metals for over 100 years. IMs are a main source of information about the occurrence of deposits, hydrothermal and weathering changes, as well as bedrock source and type. Since 2013, base metal mineral exploration has taken place on New Guinea Island (the Indonesian part). The analysis of chromian spinels as IM in beach and river sediments led to the discovery of rich chromian-bearing deposits in the Botawa River sediments. The dominant detrital minerals include chromian spinels, olivine, pyroxenes and serpentine. The source of chromian spinels, olivine and pyroxenes are most likely peridotites from the Earth's mantle zone of the ophiolite series, generated under supra-subduction conditions. The terrigenous deposits contain metamorphic minerals, such as staurolites, andalusites, epidotes, amphiboles and fragments of micas, quartz and chlorite schists. Using ICP-MS analysis of the beach sands, the concentration of Cr2O3 was determined to be at the level of 1.17%, while in the heavy minerals concentrate from the Botawa River sediment, the content of Cr2O3 amounts to 24.83%. The authors conclude that the west parts of the Van Rees Mountains are the probable parent rocks for chromium-bearing sediments. [ABSTRACT FROM AUTHOR]

The Boqueirão granitic pegmatite, alias Alto da Cabeça pegmatite, is situated in Borborema Pegmatitic Province (BPP) in Northeast Brazil. This pegmatitic province hosts globally important reserves of tantalum and beryllium, as well as significant quantities of gemstones, including aquamarine, morganite, and the high-quality turquoise-blue "Paraíba Elbaite". The studied lithium-cesium-tantalum Boqueirão granitic pegmatite intruded meta-conglomerates of the Equador Formation during the late Cambrian (502.1 ± 5.8 Ma; 40Ar/39Ar plateau age of muscovite). The pegmatite exhibits a typical zonal mineral pattern with four defined zones (Zone I: muscovite, tourmaline, albite, and quartz; Zone II: K-feldspar (microcline), quartz, and albite; Zone III: perthite crystals (blocky feldspar zone); Zone IV: massive quartz). Huge individual beryl, spodumene, tantalite, and cassiterite crystals are common as well. Microscopic examinations revealed that melt inclusions were entrapped simultaneously with fluid inclusions, suggesting the magmatic–hydrothermal transition. The magmatic–hydrothermal transition affected the evolution of the pegmatite, segregating volatile compounds (H2O, CO2, N2) and elements that preferentially partition into a fluid phase from the viscous silicate melt. Fluid inclusion studies on microcline and associated quartz combined with microthermometry and Raman spectroscopy gave an insight into the P-T-X characteristics of entrapped fluids. The presence of spodumene without other LiAl(SiO3)2 polymorphs and constructed fluid inclusion isochores limited the magmatic–hydrothermal transition at the gem-bearing Boqueirão granitic pegmatite to the temperature range between 300 and 415 °C at a pressure from 1.8 to 3 kbar. [ABSTRACT FROM AUTHOR]

Greece contains several gem corundum deposits set within diverse geological settings, mostly within the Rhodope (Xanthi and Drama areas) and Attico-Cycladic (Naxos and Ikaria islands) tectono-metamorphic units. In the Xanthi area, the sapphire (pink, blue to purple) deposits are stratiform, occurring within marble layers alternating with amphibolites. Deep red rubies in the Paranesti-Drama area are restricted to boudinaged lenses of Al-rich metapyroxenites alternating with amphibolites and gneisses. Both occurrences are oriented parallel to the ultra-high pressure/high pressure (UHP/HP) Nestos suture zone. On central Naxos Island, colored sapphires are associated with desilicated granite pegmatites intruding ultramafic lithologies (plumasites), occurring either within the pegmatites themselves or associated metasomatic reaction zones. In contrast, on southern Naxos and Ikaria Islands, blue sapphires occur in extensional fissures within Mesozoic metabauxites hosted in marbles. Mineral inclusions in corundums are in equilibrium and/or postdate corundum crystallization and comprise: spinel and pargasite (Paranesti), spinel, zircon (Xanthi), margarite, zircon, apatite, diaspore, phlogopite and chlorite (Naxos) and chloritoid, ilmenite, hematite, ulvospinel, rutile and zircon (Ikaria). The main chromophore elements within the Greek corundums show a wide range in concentration: the Fe contents vary from (average values) 1099 ppm in the blue sapphires of Xanthi, 424 ppm in the pink sapphires of Xanthi, 2654 ppm for Paranesti rubies, 4326 ppm for the Ikaria sapphires, 3706 for southern Naxos blue sapphires, 4777 for purple and 3301 for pink sapphire from Naxos plumasite, and finally 4677 to 1532 for blue to colorless sapphires from Naxos plumasites, respectively. The Ti concentrations (average values) are very low in rubies from Paranesti (41 ppm), with values of 2871 ppm and 509 in the blue and pink sapphires of Xanthi, respectively, of 1263 ppm for the Ikaria blue sapphires, and 520 ppm, 181 ppm in Naxos purple, pink sapphires, respectively. The blue to colorless sapphires from Naxos plumasites contain 1944 to 264 ppm Ti, respectively. The very high Ti contents of the Xanthi blue sapphires may reflect submicroscopic rutile inclusions. The Cr (average values) ranges from 4 to 691 ppm in the blue, purple and pink colored corundums from Naxos plumasite, is quite fixed (222 ppm) for Ikaria sapphires, ranges from 90 to 297 ppm in the blue and pink sapphires from Xanthi, reaches 9142 ppm in the corundums of Paranesti, with highest values of 15,347 ppm in deep red colored varieties. Each occurrence has both unique mineral assemblage and trace element chemistry (with variable Fe/Mg, Ga/Mg, Ga/Cr and Fe/Ti ratios). Additionally, oxygen isotope compositions confirm their geological typology, i.e., with, respectively δ18O of 4.9 ± 0.2‰ for sapphire in plumasite, 20.5‰ for sapphire in marble and 1‰ for ruby in mafics. The fluid inclusions study evidenced water free CO2 dominant fluids with traces of CH4 or N2, and low CO2 densities (0.46 and 0.67 g/cm3), which were probably trapped after the metamorphic peak. The Paranesti, Xanthi and central Naxos corundum deposits can be classified as metamorphic sensu stricto (s.s.) and metasomatic, respectively, those from southern Naxos and Ikaria display atypical magmatic signature indicating a hydrothermal origin. Greek corundums are characterized by wide color variation, homogeneity of the color hues, and transparency, and can be considered as potential gemstones. [ABSTRACT FROM AUTHOR]

Gemstones form in metamorphic, magmatic, and sedimentary rocks. In sedimentary units, these minerals were emplaced by organic and inorganic chemical processes and also found in clastic deposits as a result of weathering, erosion, transport, and deposition leading to what is called the formation of placer deposits. Of the approximately 150 gemstones, roughly 40 can be recovered from placer deposits for a profit after having passed through the "natural processing plant" encompassing the aforementioned stages in an aquatic and aeolian regime. It is mainly the group of heavy minerals that plays the major part among the placer-type gemstones (almandine, apatite, (chrome) diopside, (chrome) tourmaline, chrysoberyl, demantoid, diamond, enstatite, hessonite, hiddenite, kornerupine, kunzite, kyanite, peridote, pyrope, rhodolite, spessartine, (chrome) titanite, spinel, ruby, sapphire, padparaja, tanzanite, zoisite, topaz, tsavorite, and zircon). Silica and beryl, both light minerals by definition (minerals with a density less than 2.8–2.9 g/cm3, minerals with a density greater than this are called heavy minerals, also sometimes abbreviated to "heavies". This technical term has no connotation as to the presence or absence of heavy metals), can also appear in some placers and won for a profit (agate, amethyst, citrine, emerald, quartz, rose quartz, smoky quartz, morganite, and aquamarine, beryl). This is also true for the fossilized tree resin, which has a density similar to the light minerals. Going downhill from the source area to the basin means in effect separating the wheat from the chaff, showcase from the jeweler quality, because only the flawless and strongest contenders among the gemstones survive it all. On the other way round, gem minerals can also be used as pathfinder minerals for primary or secondary gemstone deposits of their own together with a series of other non-gemmy material that is genetically linked to these gemstones in magmatic and metamorphic gem deposits. All placer types known to be relevant for the accumulation of non-gemmy material are also found as trap-site of gemstones (residual, eluvial, colluvial, alluvial, deltaic, aeolian, and marine shelf deposits). Running water and wind can separate minerals according to their physical-chemical features, whereas glaciers can only transport minerals and rocks but do not sort and separate placer-type minerals. Nevertheless till (unconsolidated mineral matter transported by the ice without re-deposition of fluvio-glacial processes) exploration is a technique successfully used to delineate ore bodies of, for example, diamonds. The general parameters that matter during accumulation of gemstones in placers are their intrinsic value controlled by the size and hardness and the extrinsic factors controlling the evolution of the landscape through time such as weathering, erosion, and vertical movements and fertility of the hinterland as to the minerals targeted upon. Morphoclimatic processes take particular effect in the humid tropical and mid humid mid-latitude zones (chemical weathering) and in the periglacial/glacial and the high-altitude/mountain zones, where mechanical weathering and the paleogradients are high. Some tectono-geographic elements such as unconformities, hiatuses, and sequence boundaries (often with incised valley fills and karstic landforms) are also known as planar architectural elements in sequence stratigraphy and applied to marine and correlative continental environments where they play a significant role in forward modeling of gemstone accumulation. The present study on gems and gemstone placers is a reference example of fine-tuning the "Chessboard classification scheme of mineral deposits" (Dill 2010) and a sedimentary supplement to the digital maps that form the core of the overview "Gemstones and geosciences in space and time" (Dill and Weber 2013). [ABSTRACT FROM AUTHOR]