Garnets from Val d’Ala Rodingites, Piedmont, Italy: An Investigation of Their Gemological, Spectroscopic and Crystal Chemical Properties

: In Val d’Ala (Piedmont, Western Alps, Italy), the more interesting rocks for the mineralogical research are represented by rodingites (rich in mineralized veins and fractures) associated with serpentinites in the eclogitized oceanic crust of Piemonte Zone, south of Gran Paradiso Massif. Among the vein-ﬁlling minerals, garnets are the most appreciated as mineral specimens and, in less degree despite their vivid and rich colors, for their potential as gem-quality materials. This study provides a complete gemological characterization of ﬁve faceted samples and o ﬀ ers new information by means of Synchrotron X-ray computed micro-tomography imaging gem features. Electron-probe microanalysis (EMPA) and laser ablation–inductively coupled plasma–mass spectrometry (LA–ICP–MS) established that the chemical composition of garnets from di ﬀ erent localities, resulted both close to pure andradite, enriched in light rare earth elements (LREE) with a positive Eu anomaly, and grossular-andradite solid solution (grandite), enriched in heavy rare earth elements (HREE). X-ray powder di ﬀ raction analyses indicate the possible coexistence of almost pure grossular and andradite. A spectroscopic approach, commonly used with gem-like material, by Raman and di ﬀ use reﬂectance infrared Fourier transform (DRIFT) spectroscopy, completes the characterization of the samples. The new data on the textural and geochemical features of the grandite and andradite garnets suggest local growth processes under various chemical and oxidation conditions of metasomatic and metamorphic ﬂuids interacting with the host-rocks. Garnets represent long-lasting mineral records of the complex geological history of the Val d’Ala rodingitic dikes during their oceanic- and subduction-related metamorphic evolution.


Introduction
Val d'Ala (Piedmont, Italy) is internationally renowned for mining activity of minerals used for practical and decorative purposes. The more interesting minerals, garnet, "mussite" (a fibrous variety name of diopside), vesuvianite, and epidote have been well known since the 18th century. The orange-brown grossular-garnets, known with the variety name "hessonite", were used in the past as precious gemstones in the traditional costumes of the valley and as a sign of engagement. The grossular In the first decades of last century, detailed studies have been performed mainly focusing on the morphological and chemical properties of the garnet, and on the more notable occurrences of rodingite layers and lenses along the valley, representing the main sources of high-quality crystals [1][2][3]. Recently, Maletto and Piccoli [4] published a monograph of great interest for museum and private collections dedicated to all Val d'Ala minerals.
The significant scientific and economic value of garnet from Val d'Ala is documented in literature, even if in recent times the mineralogical, petrological, and structural investigations on this mineral are lacking. In this light, we have undertaken this study, aimed to provide a complete mineralogical and gemological characterization that may enhance their potential use as gem material and their role in metamorphism. The chemical and physical properties elucidated in this study may further the understanding of the metamorphic kinematics experienced by the Val d'Ala ultramafic and rodingite host rocks, and their evolution in the subduction of Mesozoic ocean lithosphere during the Alpine orogeny. In particular, the different geodynamic environments in which rodingites can form must be considered. In fact, rodingites are Si-undersaturated and Ca-rich rocks that can form as a result of the metasomatic interaction between serpentinites and mafic dykes at the ocean floor or after fluid-assisted recrystallization during subduction and collision [5][6][7][8][9][10][11][12][13][14]. Garnet is indeed a litmus paper as it is always present in the diagnostic assemblages in each of these different petrogenetic environments.
The studied samples belong to the Bazzi historical collection preserved in the Museum of the Department of Earth Sciences of the University of Milan, Italy. The faceted samples were characterized by standard gemological methods, Synchrotron X-ray computed micro-tomography (SR-μCT) and Raman spectroscopy. Mineral fragments coming from the same localities and garnet country-rocks were analyzed In the first decades of last century, detailed studies have been performed mainly focusing on the morphological and chemical properties of the garnet, and on the more notable occurrences of rodingite layers and lenses along the valley, representing the main sources of high-quality crystals [1][2][3]. Recently, Maletto and Piccoli [4] published a monograph of great interest for museum and private collections dedicated to all Val d'Ala minerals.
The significant scientific and economic value of garnet from Val d'Ala is documented in literature, even if in recent times the mineralogical, petrological, and structural investigations on this mineral are lacking. In this light, we have undertaken this study, aimed to provide a complete mineralogical and gemological characterization that may enhance their potential use as gem material and their role in metamorphism. The chemical and physical properties elucidated in this study may further the understanding of the metamorphic kinematics experienced by the Val d'Ala ultramafic and rodingite host rocks, and their evolution in the subduction of Mesozoic ocean lithosphere during the Alpine orogeny. In particular, the different geodynamic environments in which rodingites can form must be considered. In fact, rodingites are Si-undersaturated and Ca-rich rocks that can form as a result of the metasomatic interaction between serpentinites and mafic dykes at the ocean floor or after fluid-assisted recrystallization during subduction and collision [5][6][7][8][9][10][11][12][13][14]. Garnet is indeed a litmus paper as it is always present in the diagnostic assemblages in each of these different petrogenetic environments.
The studied samples belong to the Bazzi historical collection preserved in the Museum of the Department of Earth Sciences of the University of Milan, Italy. The faceted samples were characterized by standard gemological methods, Synchrotron X-ray computed micro-tomography (SR-µCT) and Raman spectroscopy. Mineral fragments coming from the same localities and garnet country-rocks were analyzed by X-ray powder diffraction (XRPD), diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), and electron microprobe (EMPA-WDS) combined with laser ablation-inductively coupled plasma-mass (LA-ICP-MS) techniques.

Geological Setting
Val d' Ala ( Figure 2) is an east valley underlain by metaophiolites of the Piemonte Zone of the Western Alps between the Gran Paradiso (to the North) and Dora-Maira Penninic continental nappes. These Mesozoic oceanic rock sequences mainly consist of ultramafites, metagabbros, metabasalts, and calcschists, which underwent Alpine metamorphism under greenschist-and blueschists-facies conditions. These multiple facies reflect the polyphase evolution recorded from Mesozoic ocean lithosphere deformation in the Tertiary Alpine subduction and collisional tectonics ( [15][16][17] and references therein). During Alpine subduction, Val d'Ala metaophiolites re-equilibrated at P ≥ 1.3 GPa and T = 425-550 • C, as estimated from eclogite relics variably preserved during exhumation-related greenschist-facies [17]. Mineral assemblages of metabasites and ultramafites ( [15][16][17] and references therein) indicate that these ophiolites recorded an ocean floor-related metamorphic imprint, under conditions (zeolite-, prehnite-pumpellyite-and greenschist-facies) similar to those suggested for other metaophiolites from Western Alps [10]. Their qualitative PT (Pressure-Temperature) evolution as deduced from the literature is synthesized in Figure 2d where the low-and high-pressure stability fields of different garnet-bearing assemblages inferred from polymetamorphic rodingites of Betic Cordillera, in Southern Spain [18] are reported (light-pink fields). The ultramafic rocks consist of antigorite serpentinite bodies that represent the most widespread rock-type of Val d'Ala, and contain from decametric to metric lenses and layers of rodingites. These rocks are intersected by abundant veins that have attracted the interest of many researchers since the beginning of 1800 ( [6,19] and references therein). Rodingites occur in many localities all along Val d'Ala, from the high part of the valley, West of the village of Balme, to the lower part of the valley, East of the village of Ala di Stura near Mount Curbassera. In all occurrences, the rodingites are very heterogeneous with structural and mineralogical features that record a complex tectonic origin. The rodingite-forming minerals are mainly Ca-rich garnet, epidote, diopside, chlorite, and vesuvianite, with minor titanite and opaque minerals [16]. A complete list of all the minerals as well as the detailed description of the main occurrences of rodingites are already reported by [3]. The mineralogical richest and most known locations for finest grossular are Testa Ciarva and Roch Neir (I and II; labelled No.1, 2, and 3 in Figure 2c) where the serpentinite cliffs contain rodingite layers up to 2 m that are commonly boudinaged. South of Roch Neir, in Mount Tovo serpentinites (labelled 4 in Figure 2c), mineralized veins host garnets with a rounded and globular shape. Finally at Curbassera (labelled 5 in Figure 2c), grossular concentrations occur both in lenses of brown rodingite and in blocks of debris in a landslide fallen in the 18th century. Our samples came from the above-mentioned famous localities.  [16,20]. Legend: Metaophiolites of the Piemonte Zone: 1 = calcschist; 2 = metabasalt; 3 = metagabbro; 4 = serpentinite; 5 = metagranitoid with K-feldspar porphyroclasts (Gran Paradiso nappe-Penninic continental crust); 6 = fine-grained gneiss (Sesia-Lanzo Zone-Austroalpine continental crust); sampling localities: red asterisks: 1 = Testa Ciarva; 2, 3 = Roch Neir I, II; 4 = Mount Tovo; 5 =Curbassera. (d) Qualitative P-T evolution of Val d'Ala metaophiolites as inferred from [10,17]. See discussion in the text. Orange square = estimated metamorphic conditions of eclogite facies in Val d'Ala [17]. Metamorphic facies are after [21]: A = amphibolite, Bs = blueschist, E = eclogite, EA = epidote-amphibolite, G = granulite, Gs = greenschist, PP = prehnite-pumpellyite, Z = zeolite. Light-pink fields = low-and high-pressure conditions for garnet growth in polymetamorphic rodingites from Betic Cordillera-Southern Spain [18].

Materials and Methods
Twelve samples from different localities were selected for this study and are described in Table 1. The samples range from light yellow to dark red in color. The reddish garnets, from 1 cm to 3 cm in size with various crystalline faces (cube, trapezoedron, rhombic-dodecahedron, and hexoctahedron), may be deformed whereas the light yellow samples are smaller, up to 4 mm in size, clear and only rhombic-dodecahedron in shape. Five faceted samples (three from Roch Neir II, samples 8-10, and two from Testa Ciarva, samples 11,12) were examined by standard gemological methods at the laboratories of the University of Pavia, Italy, in order to determine their refractive index, hydrostatic specific gravity and microscopic features. The refractive indices were measured with a Krüss refractometer (1.45-1.80 range) using ordinary light source with a sodium filter (589 nm) and a methylene iodide as a contact liquid (n = 1.80). A Mettler hydrostatic balance was used to determine the specific gravity in bi-distilled water. The ultraviolet fluorescence was investigated with a short (254 nm) and long (366 nm) wavelength ultraviolet Wood lamp. The color was determined with a GIA Color Table; often the crystals are slight polychrome.
The Microfocus X-ray computed micro-tomography (CT) analyses of two cut samples (10 and 11) were performed at laboratory X-ray µCT scanning using the TomoLab station at the Elettra synchrotron facility in Basovizza (Trieste, Italy). The µCT system is equipped with a sealed microfocus X-ray source (L9181, Hamamatsu Photonic, Iwata, Japan) and delivers a polychromatic beam in a Voltage range of 40 kV to 130 kV with a maximum current of 300 µA and a minimum focal spot size of 5 µm. The used detector consisted of a full frame CCD imager (4008 × 2672 pixels) coupled to a Gadox scintillator screen by a fiber-optic taper. The water-cooled CCD camera has a 12-bit dynamic range and an effective pixel size of 12.5 µm 2 × 12.5 µm 2 . The experimental parameters used for the X-ray µCT scans are reported in Table 2. The slice reconstruction was carried out using the commercial software COBRA (Exxim Computing, Pleasanton, CA, USA) based on the Feldkamp algorithm [22], which also allows us to correct beam hardening artefacts [23]. 3D visualization through volume rendering of the analyzed samples were obtained by the commercial software VGStudio 2.2 (Volume Graphics). Table 2. Experimental parameters used for the laboratory X-ray microtomography measurements (d 1 and d 2 represent the source-to-sample and the source-to-detector distances, respectively). Seven samples from different localities were polished and analyzed by electron microprobe (EMPA) and inductively coupled plasma-mass spectroscopy (LA-ICP-MS): five massive garnets samples varying from 1-2 mm (2 and 7) to 3-4 cm in size (1, 4 and 5) embedded in epoxy resin, and two thin sections (3 and 6) of rock containing garnets in their matrix.

Sample
Backscattered electron (BSE) images and quantitative chemical analyses of major and minor elements were obtained with the JEOL JXA-8200 electron microprobe in wavelength dispersion mode (EMPA-DS) at the laboratory of the Department of Earth Sciences of the University of Milan, Italy, under the following conditions: 15 kV accelerating voltage, 5 nA beam current, and a count time of 60 s on peak and 30 s on the background, with a 1 µm diameter beam. Natural minerals were used as standards and the rough data corrected for matrix effects using a conventional ΦρZ routine in the JEOL software package (Japan Electron Optics Laboratory).
Rare earth and selected trace elements were determined by laser ablation-inductively coupled plasma-mass spectroscopy (LA-ICP-MS) at IGG-CNR Laboratory of Pavia, Italy. Wherever possible measurement spots were chosen at the same or close to the EMPA points. The instrument consisted of a 193 nm Excimer laser (Geolas) coupled to an Agilent 8900 triple quadrupole ICPMS. The spot size was 55 µm, using NIST SRM 610 glass as an external standard and 29 Si as an internal standard, as analyzed by microprobe. Precision and accuracy estimated on the USGS basaltic glass standard BCR2 and NIST612 were better than 10%.
Four fragments (~500 µm) from samples 1-3, and 7 were selected for powder X-ray diffraction measurements. The analyses were performed at the Department of Earth Sciences of the University of Milan, by a Panalytical X'Pert-PROMPD X'Celerator X-ray powder diffractometer, using CuKα radiation (λ = 1.518 Å), at a beam voltage of 40 kV and a current of 40 mA. X-ray powder diffraction patterns were collected over the 9-120 • range of the scattering angle 2θ, with steps of 0.01 • 2θ and a count time of 50 s per step. The lattice parameters of the garnet samples were determined by using Si (NBS SRM 640b) as an internal standard and the General Structure Analysis System (GSAS) software was used to process XRPD data [24,25].
Besides standard gemological testing, four faceted samples were analyzed by Raman spectroscopy at the laboratories of the University of Pavia. Micro-Raman scattering measurements were conducted using a Horiba Jobin-Yvon Xplora Plus single monochromator spectrometer (with a grating of 2400 groove/mm) equipped with an Olympus BX41 microscope. Raman spectra were excited by the 532 nm line. The spectrometer was calibrated to the silicon Raman peak at 520.5 cm -1 . The spectral resolution was~2 cm -1 and the instrumental accuracy in determining the peak positions was 0.56 cm -1 . Raman spectra were collected in the spectral range 50-1250 cm -1 and 3000-3800 cm -1 for 5 s averaging over 40 accumulations. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) was performed on four samples at the Italian Gemological Institute (IGI), using a Perkin Elmer Frontier FTIR, equipped with the Praying Mantis diffuse reflection accessory. The spectra of the samples (2-4, and 7) were collected between 8000 cm -1 to 450 cm -1 , using LiTaO 3 as detector. A resolution of 4 cm -1 was adopted and a total of 128 scans were recorded and averaged for each sample.

Gemological Properties and 3D Visualisation
The vivid, intense and rich colors, ranging from reddish orange to orange red, make the faceted samples of gemological interest (Figure 3). The luster is vitreous; the diaphaneity is transparent/translucent. The gems have been cut from samples with a combination of the rhombic dodecahedron {100} and trapezohedron {211} crystal form. The inhomogeneous color of some samples may be due to the presence of crystalline inclusions such as clinochlore, diopside, calcite veinlets, or fractures. Their physical and optical properties are reported in Table 3. The measured gravity ranges from 3.63 g/cm 3 to 3.66 g/cm 3 , in agreement with the literature data for solid solution grossular/andradite [26]. All the analyzed gems are inert to long and short UV. step. The lattice parameters of the garnet samples were determined by using Si (NBS SRM 640b) as an internal standard and the General Structure Analysis System (GSAS) software was used to process XRPD data [24,25]. Besides standard gemological testing, four faceted samples were analyzed by Raman spectroscopy at the laboratories of the University of Pavia. Micro-Raman scattering measurements were conducted using a Horiba Jobin-Yvon Xplora Plus single monochromator spectrometer (with a grating of 2400 groove/mm) equipped with an Olympus BX41 microscope. Raman spectra were excited by the 532 nm line. The spectrometer was calibrated to the silicon Raman peak at 520.5 cm -1 . The spectral resolution was 2 cm -1 and the instrumental accuracy in determining the peak positions was 0.56 cm -1 . Raman spectra were collected in the spectral range 50-1250 cm -1 and 3000-3800 cm -1 for 5 s averaging over 40 accumulations.
Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) was performed on four samples at the Italian Gemological Institute (IGI), using a Perkin Elmer Frontier FTIR, equipped with the Praying Mantis diffuse reflection accessory. The spectra of the samples (2-4, and 7) were collected between 8000 cm -1 to 450 cm -1 , using LiTaO3 as detector. A resolution of 4 cm -1 was adopted and a total of 128 scans were recorded and averaged for each sample.

Gemological Properties and 3D Visualisation
The vivid, intense and rich colors, ranging from reddish orange to orange red, make the faceted samples of gemological interest (Figure 3). The luster is vitreous; the diaphaneity is transparent/translucent. The gems have been cut from samples with a combination of the rhombic dodecahedron {100} and trapezohedron {211} crystal form. The inhomogeneous color of some samples may be due to the presence of crystalline inclusions such as clinochlore, diopside, calcite veinlets, or fractures. Their physical and optical properties are reported in Table 3. The measured gravity ranges from 3.63 g/cm 3 to 3.66 g/cm 3 , in agreement with the literature data for solid solution grossular/andradite [26]. All the analyzed gems are inert to long and short UV.  Table 3. Figure 3. Faceted garnets described in Table 3. More details were provided by the 3D visualisation of faceted samples 10 and 11 and their renderings are shown in Figure 4. In Figure 4a, the tomographic results highlight the occurrence of small and irregular crystals (labeled garnet 11-2) widespread on the surface of the gem (garnet 11-1). The lighter gray-scale values associated to garnet 11-2 might reflect its slightly different chemical composition with respect to garnet 11-1 and attributed to the presence of a Fe-richer phase. This hypothesis is consistent with the XRPD refinement results of sample 3 from the same locality, indicating the coexistence both of grossular and of andradite (see below; Section 4.2).  More details were provided by the 3D visualisation of faceted samples 10 and 11 and their renderings are shown in Figure 4. In Figure 4a, the tomographic results highlight the occurrence of small and irregular crystals (labeled garnet 11-2) widespread on the surface of the gem (garnet 11-1). The lighter gray-scale values associated to garnet 11-2 might reflect its slightly different chemical composition with respect to garnet 11-1 and attributed to the presence of a Fe-richer phase. This hypothesis is consistent with the XRPD refinement results of sample 3 from the same locality, indicating the coexistence both of grossular and of andradite (see below; 4.2 paragraph).
Furthermore, the 3D rendering with the corresponding iso-surfaces of the fractures and pores of sample 10 are shown in Figure 4b. A widespread microcracking is highlighted inside the garnet and is characterized by cracks mostly iso-oriented. Pores appear micrometric in size with an irregular shape and randomly distributed inside the whole volume. The reconstructed slices show that the cracks are mostly empty and, only in few cases, are filled with mineral phases, which have grayscale values very similar to garnet 11-2 and could be attributed to the crystallization of andradite.

Chemical Composition and Crystallographic Properties
We analyzed five massive samples and two thin sections where the mineral paragenesis consists mainly of garnet, diopside, clinochlore, amphibole, and rutile/titanite. Fabric of the host-rodingites varies from massive to foliated, generally banded (summarized description of thin sections are synthesized in Table 4). Furthermore, the 3D rendering with the corresponding iso-surfaces of the fractures and pores of sample 10 are shown in Figure 4b. A widespread microcracking is highlighted inside the garnet and is characterized by cracks mostly iso-oriented. Pores appear micrometric in size with an irregular shape and randomly distributed inside the whole volume. The reconstructed slices show that the cracks are mostly empty and, only in few cases, are filled with mineral phases, which have grayscale values very similar to garnet 11-2 and could be attributed to the crystallization of andradite.

Chemical Composition and Crystallographic Properties
We analyzed five massive samples and two thin sections where the mineral paragenesis consists mainly of garnet, diopside, clinochlore, amphibole, and rutile/titanite. Fabric of the host-rodingites varies from massive to foliated, generally banded (summarized description of thin sections are synthesized in Table 4).
The relative quantities of grossular and andradite compared to all remaining components are plotted in Figure 5 and averaged chemical analyses for samples 2, 7, 1, 4, 5 and selected analyses for thin sections, samples 3 and 6, are reported in Table 5. The rare earth elements (REE) and trace elements concentrations are presented in Table 6. Table 4. Textural and mineralogical characters of studied thin sections from samples 3 and 6. The short side of thin sections microphotographs is 6 mm and 10 mm for samples 3 and 6, respectively.  Table 4. Textural and mineralogical characters of studied thin sections from samples 3 and 6. The short side of thin sections microphotographs is 6 mm and 10 mm for samples 3 and 6, respectively.

Mineral Assemblages Texture
Minerals 2019, 9, x FOR PEER REVIEW 9 of 19 9 Table 4. Textural and mineralogical characters of studied thin sections from samples 3 and 6. The short side of thin sections microphotographs is 6 mm and 10 mm for samples 3 and 6, respectively.  Table 4. Textural and mineralogical characters of studied thin sections from samples 3 and 6. The short side of thin sections microphotographs is 6 mm and 10 mm for samples 3 and 6, respectively.
Massive: garnet occurs in aggregates or in veins interstitial between diopside polygonal and seriate aggregates. Large grainsized diopside is cloudy and wrapped by clear fine-grained polygonal diopside grains. Garnets show complex Grs-Adr zoning (different gray patchy zones in the BSE image on the left) that are intersected by late Adr-rich veins.
Foliated: garnetite vein at high angle with the Alpine foliation that is marked by chlorite-diopside lenticular aggregates and garnet trails and elongated aggregates. Compositional pattern of garnet is complex: in garnetite veins Adrrich grains occur, whereas in finegrained aggregates complex and oscillatory Grs-Adr zoning occurs, as shown in the BSE image on the left.
Foliated: garnetite vein at high angle with the Alpine foliation that is marked by chlorite-diopside lenticular aggregates and garnet trails and elongated aggregates. Compositional pattern of garnet is complex: in garnetite veins Adr-rich grains occur, whereas in fine-grained aggregates complex and oscillatory Grs-Adr zoning occurs, as shown in the BSE image on the left.  Table 4. Textural and mineralogical characters of studied thin sections from samples 3 and 6. The short side of thin sections microphotographs is 6 mm and 10 mm for samples 3 and 6, respectively.  10 thin sections, samples 3 and 6, are reported in Table 5. The rare earth elements (REE) and trace elements concentrations are presented in Table 6. The deficiency of silica (stoichiometric Si values lower than 6 in Table 5) may indicate the possible occurrence of OH in the tetrahedral site supporting the presence of water as resulted from the Raman spectra (see below).   The deficiency of silica (stoichiometric Si values lower than 6 in Table 5) may indicate the possible occurrence of OH in the tetrahedral site supporting the presence of water as resulted from the Raman spectra (see below).

Mineral Assemblages Texture
The results show two different compositions of garnets. The first group, including samples 2 and 7, is very close to the end member andradite; the second one (massive samples 1, 4, 5 and thin sections 3 and 6) belongs to a solid solution grossular-andradite (grandite), never reaching the grossular pure end member.
The aspect and the analyses of sample 2 (Adr 96 ) from Roch Neir II confirm the previous classification of garnet as topazolite, the variety of andradite greenish-yellow in color. Sample 7 from Mount Tovo with globular and rounded crystal shapes, reported in literature as grossular [3], is here determined to be 95-99% andradite. Sample 7 exhibits a hue of color ranging from green to orange-brown with higher content of the chromophore minor elements, such as Ti, Cr, and V. The higher content of these elements was determined in the brown zones of the crystals.
In the second group, including samples from deep red-brown to light orange in color and classified as hessonite variety, grossular content ranges from 41% to 88%, andradite content from 4% to 48% and almandine up to 20%. The higher grossular component was detected in samples from Testa Ciarva (sample 3) and Curbassera (sample 6) where garnets consist of large red brown crystals covered by smaller garnet crystals paler in color in respect to the samples from Roch Neir I (1), II (4,5). The TiO 2 content is up to 2.4 wt %, Cr 2 O 3 ranges from nil to 0.1 wt %, and MnO from 0.3 wt % to 0.8 wt %. The variations, occurring in all samples, are not related to a regular or harmonic zoning from core to the rim. The lower content of chromophore elements (Ti, V, and Cr) of sample 3 (Testa Ciarva) may explain the color of faceted samples 11 and 12 coming from the same locality, lighter than those from Roch Neir II (9)(10)(11).
Chondrite-normalized REE patterns [28] of the examined samples are plotted, as mean values, in Figure 7a. The patterns of grandite garnets (1,3,6) display an increase of heavy rare earth elements (HREE) and well match that of grossular garnet. In contrast, andradite samples (2,7) show the enrichment in LREE with respect to HREE. As already discussed by [29] this behavior is controlled by crystal chemistry and indicate that in a calcic garnet the substitution of Fe 3+ for Al at the [Y] site enlarges the eightfold [X] site and favors the incorporation of LREE. Moreover, the positive Eu anomaly, more evident in sample 7 and in the andradite-rich areas of sample 3, implies the presence of Eu in the reduced form (Eu 2+ ) according with the reaction Fe 2+ + Eu 3+  Fe 3+ + Eu 2+ [30] and its fractionation from the HREE.
In all samples, total REE content correlates positively with Y indicating, at least at local level, an equilibrium state [31]. Yttrium is plotted in the chondrite-normalized diagram together with the  Table 5.
Chondrite-normalized REE patterns [28] of the examined samples are plotted, as mean values, in Figure 7a. The patterns of grandite garnets (1,3,6) display an increase of heavy rare earth elements (HREE) and well match that of grossular garnet. In contrast, andradite samples (2,7) show the enrichment in LREE with respect to HREE. As already discussed by [29] this behavior is controlled by crystal chemistry and indicate that in a calcic garnet the substitution of Fe 3+ for Al at the [Y] site enlarges the eightfold [X] site and favors the incorporation of LREE. Moreover, the positive Eu anomaly, more evident in sample 7 and in the andradite-rich areas of sample 3, implies the presence of Eu in the reduced form (Eu 2+ ) according with the reaction Fe 2+ + Eu 3+ → Fe 3+ + Eu 2+ [30] and its fractionation from the HREE. The calculated a unit-cell parameter from XRPD analyses, crystallite size and microstrain of the four analyzed samples are reported in Table 7. The a-value of samples 2 and 7 are in agreement with the end-member andradite, whereas in sample 1 the cell edge results between the grossular and andradite values reported in literature (andradite a = 12.0630(1) Å, value from [32]; grossular a = 11.8505(4) Å, value from [33]). XRPD pattern of sample 3 suggests the coexistence of two separate garnets, an almost pure grossular (3-1) associated with an andradite . Note the occurrence of a second generation of little light yellow andradite-garnets formed on the older and bigger red grossular as suggested by [3].
The microstructural features of garnet 3-2 were not reported because of the low statistics of its diffraction peaks in the XRPD pattern that do not allow us to obtain reliable microstructural results.
The mean crystal size is larger for grossular (3-1) and andradite (2,7) than for the most intermediate grossular-andradite solid solution (1), reflecting the larger coherence of their diffracting domains. Conversely, the microstrain is smaller for grossular (3-1) and andradite (2,7) whereas the intermediate solid solution shows smaller crystallite sizes and larger strain values. In all samples, total REE content correlates positively with Y indicating, at least at local level, an equilibrium state [31]. Yttrium is plotted in the chondrite-normalized diagram together with the concentrations of Sr, Zr and of trace elements forming the "first transition series" (i.e., Sc, Ti, V, Cr, Co, Ni, and Zn), arranged according to the atomic number increasing (Figure 7b). The patterns are typically U-shaped and in all samples Cr, Co, Ni, Zn, and Y are below the C1 values whereas Sc, Ti, V, and Zr show a slight enrichment mainly in grandites. Other measured trace elements (Cs, Ba, Pb, Nb, Hf, Ta, Th, and U) resulted below the detection limits.
The calculated a unit-cell parameter from XRPD analyses, crystallite size and microstrain of the four analyzed samples are reported in Table 7. The a-value of samples 2 and 7 are in agreement with the end-member andradite, whereas in sample 1 the cell edge results between the grossular and andradite values reported in literature (andradite a = 12.0630(1) Å, value from [32]; grossular a = 11.8505(4) Å, value from [33]). XRPD pattern of sample 3 suggests the coexistence of two separate garnets, an almost pure grossular (3-1) associated with an andradite . Note the occurrence of a second generation of little light yellow andradite-garnets formed on the older and bigger red grossular as suggested by [3]. The microstructural features of garnet 3-2 were not reported because of the low statistics of its diffraction peaks in the XRPD pattern that do not allow us to obtain reliable microstructural results.
The mean crystal size is larger for grossular (3-1) and andradite (2,7) than for the most intermediate grossular-andradite solid solution (1), reflecting the larger coherence of their diffracting domains. Conversely, the microstrain is smaller for grossular (3-1) and andradite (2,7) whereas the intermediate solid solution shows smaller crystallite sizes and larger strain values.
The presence of garnets with different morphology and crystal-chemistry is related to changing of chemical and physical conditions during the calcic metasomatism, which represents the main cause of the occurrence of rodingites in this area and/or during the subsequent Alpine deformation and metamorphism. The grandite garnets probably were formed in presence of low f O 2 fluids (low Adr/Alm ratio) during the serpentinization of the host rocks. On the contrary, the smaller and well-shaped andradites may be the product of an increase of fluid activity (f O 2~H M buffer) producing a progressive Al mobility and removal, accompanied by a significant increase in the iron oxidation (high Adr/Alm ratio) [18,34,35].

Raman and DRIFT Spectroscopy
We analyzed all the faceted garnets using the Raman spectroscopy from 100 cm -1 to 1100 cm -1 and from 3500 cm -1 to 3700 cm -1 ; the range 100-1100 cm -1 is usually divided for garnets in two regions: the first below 400 cm -1 (internal vibrations) and the second above 400 cm -1 (external vibration region). All the spectra resulted very similar, so only that relative to sample 9 is shown in Figure 8. The presence of garnets with different morphology and crystal-chemistry is related to changing of chemical and physical conditions during the calcic metasomatism, which represents the main cause of the occurrence of rodingites in this area and/or during the subsequent Alpine deformation and metamorphism. The grandite garnets probably were formed in presence of low fO2 fluids (low Adr/Alm ratio) during the serpentinization of the host rocks. On the contrary, the smaller and well-shaped andradites may be the product of an increase of fluid activity (fO2~HM buffer) producing a progressive Al mobility and removal, accompanied by a significant increase in the iron oxidation (high Adr/Alm ratio) [18,34,35].

Raman and DRIFT Spectroscopy
We analyzed all the faceted garnets using the Raman spectroscopy from 100 cm -1 to 1100 cm -1 and from 3500 cm -1 to 3700 cm -1 ; the range 100-1100 cm -1 is usually divided for garnets in two regions: the first below 400 cm -1 (internal vibrations) and the second above 400 cm -1 (external vibration region). All the spectra resulted very similar, so only that relative to sample 9 is shown in Figure 8.
The infrared spectra between 1100 cm -1 and 450 cm -1 of samples 2 and 7 and of samples 3 and 4 are very similar to each other. Spectra of samples 2 and 3 are shown in Figure 9. The sample 2 exhibits peaks at 888 cm -1 , 830 cm -1 and 815 cm -1 , 589 cm -1 , 511 cm -1 , and 478 cm -1 , which are related to the vibrational mode of the SiO 4 tetrahedra [43][44][45]. The position of these peaks are in agreement with measurements relative to andradite (94%) of [43] and are consistent with our chemical results on this sample (andradite 96%). Instead, the spectra of sample 3, resulted 61% grossular, shows a shift of these SiO 4 vibrational modes towards higher frequency, i.e., 908 cm -1 , 853 cm -1 and 837 cm -1 , 615 cm -1 , 538 cm -1 , and 468 cm -1 , consistent with data reported in [45] for grossular and in [43] for 74% grossular. The change of the energies of these mid-IR bands is due to difference in the chemical composition, as well known for garnets. Moreover, the analysis of the Raman spectrum in the range from 3500 cm -1 to 3700 cm -1 allowed us to determine the presence of OH, that, in grossular garnets and especially in rodingites, may be present (expressed as weight % in H2O) in a range from 12.8 wt % to less than 0.005 wt % but typically less than 0.3 wt % [39]. In Figure 8b, we can observe the internal OH-stretching modes that derive from the O4H4 groups. The OH-stretching region consists of two OH bands around 3663 cm -1 and 3600 cm -1 . The 3663 cm -1 band is connected to vibrations of O4H4 groups that are surrounded by other O4H4 groups and the 3600 cm -1 band to O4H4 clusters adjacent to their SiO4 neighbors [39]. The more complex bands at 3606 cm -1 and 3636 cm -1 are OH-stretching modes [40]. The band located at 3572 cm -1 may represent hydrogrossular substitution [41,42].
The infrared spectra between 1100 cm -1 and 450 cm -1 of samples 2 and 7 and of samples 3 and 4 are very similar to each other. Spectra of samples 2 and 3 are shown in Figure 9. The sample 2 exhibits peaks at 888 cm -1 , 830 cm -1 and 815 cm -1 , 589 cm -1 , 511 cm -1 , and 478 cm -1 , which are related to the vibrational mode of the SiO4 tetrahedra [43][44][45]. The position of these peaks are in agreement with measurements relative to andradite (94%) of [43] and are consistent with our chemical results on this sample (andradite 96%). Instead, the spectra of sample 3, resulted 61% grossular, shows a shift of these SiO4 vibrational modes towards higher frequency, i.e., 908 cm -1 , 853 cm -1 and 837 cm -1 , 615 cm -1 , 538 cm -1 , and 468 cm -1 , consistent with data reported in [45] for grossular and in [43] for 74% grossular. The change of the energies of these mid-IR bands is due to difference in the chemical composition, as well known for garnets.

Conclusions
Ca-rich garnets are the only documented garnets occurring in the rodingites of Val d'Ala. The orange-red garnets from Testa Ciarva and the light yellow colored andradite (topazolite variety) from Roch Neir I are prized among gemstone collectors. The variation in color make them very

Conclusions
Ca-rich garnets are the only documented garnets occurring in the rodingites of Val d'Ala. The orange-red garnets from Testa Ciarva and the light yellow colored andradite (topazolite variety) from Roch Neir I are prized among gemstone collectors. The variation in color make them very attractive and valuable for gemological purposes. However, the translucent diaphaneity and the presence of defects and fractures (well evidenced by the µCT) which characterize their singular charm, motivated the scarce consideration on the market for these garnets.
The complete characterization we carried out leads to the following conclusions: Chemical composition ranges from grossular-andradite solid solution to pure andradite. These compositional variations resulted irregular and indicate, together with the different size of the crystals, a growth in partial chemical equilibrium conditions, as expected in polyphasic metamorphic rocks. The crystallization of both Grs rich and pure Adr garnet suggests a change from internally buffered metamorphic conditions to infiltration processes of oxidation fluids, probably released by the hosting serpentinite, both during oceanization and subduction processes, in agreement with the metamorphic evolution inferred from the literature (Figure 2d). Indeed, Val d'Ala metaophiolites recorded low-pressure re-equilibration during Jurassic-Cretaceous oceanization, followed by eclogiteand greenschist-facies imprints during Alpine subduction and successive exhumation.
Crystallographic data highlight the coexistence of almost pure andradite and grandite very close to grossular end-member enlarging the variation range resulted from microprobe analyses.
The DRIFT spectra result adequate to the chemical compositions. Raman spectra of faceted samples resulted in andradite-grossular solid solution and evidenced the presence of OH but at a very low level.
Compositional variation, microstructure, and growth zoning of garnet may be used as a key to understanding the timing and duration of the metamorphic events or the partial chemical equilibrium during the crystallization. In a complex geological context such as that of Val d'Ala, the present data, suggest a growth of garnets during one or more metasomatic/metamorphic events, involving increasing of Ca and variation of Al and Fe mobility due to different influx of hydrothermal fluids and/or different chemical and physical interaction with the host rocks.
A forthcoming planned structural and metamorphic analysis supporting a strategic sampling, focused on defining the relative chronology of overlapping tectono-metamorphic imprints, will drive towards a comprehensive interpretation of the geological and petrological processes occurred in Val d'Ala metaophiolites.