Amethyst from Boudi, Morocco

hourglass shape. Photo by Abdelghani El Harfi and Salahaddine Mouaddib.
ABSTRACT
Amethysts from Boudi, Morocco, are characterized by double terminations and hourglass-shaped color zoning. This study provides information about the geology of the deposit, the mining of the material, and its internal and external features. Photos show the amethyst’s strong color zoning. Analysis of the needle-shaped mineral inclusions identified them as hematite, oriented along the crystal’s growth direction.
In early 2012, the Geostone Group in Casablanca obtained exclusive rights to the mine (an open quarry, in accordance with Moroccan law). The company began production in early 2013, after building an off-road track to comply with environmental regulations. This article focuses on the geological setting of the deposit and the gemological features of the amethysts obtained from it.
LOCATION AND ACCESS

Anti-Atlas mountain range of Morocco. From Faik (2005).


GEOLOGY AND MINERALOGY
The deposit is exposed along an eroded area on the south side of an anticline formed by rock of Cambrian age. It covers hundreds of square meters in a fractured area crossed by hydrothermal veins. The host rock is siltstone-sandstone belonging to the Issafen Formation of the Lower Cambrian, a schist formation composed of mudstone with marl and sandstone intercalations in the upper zone, dolomitic limestones (with stromatolites) in the middle, and purplish red mudstones in the lower part, again with intercalations of stromatolitic limestones and dolostones, all of these in stratigraphic contact. In the simplified geological map, the Issafen Formation is below the Schist-Limestone and Limestone series of Lower Cambrian age, and thus is not visible (again, see figure 4).At Boudi, quartz is found either scattered in a silt-sandstone matrix or within cavities of a complex fault and fractures system. Small openings are completely filled with interlocking quartz crystals. In the reddish mudstones, floating quartz specimens are always found as single crystals without matrix, usually singly terminated but sometimes doubly. The amethyst clearly formed by hydrothermal deposition, but the condition of the crystals suggests they were removed from the original site of crystallization and subsequently encapsulated in the mudstones. The deposit could be regarded, then, as both primary and secondary. The authors hypothesize that the well-shaped quartz crystals originated in the faults and veins in the surrounding limestone, and then eroded and redeposited in the residual mudstones.
MINING


DESCRIPTION OF THE AMETHYST
Amethyst from Boudi displays a fairly typical morphology. The crystals have well-developed prism faces, and in some cases they present the double termination that characterizes the locality. Rhombohedral faces are well developed (figure 7). Euhedral crystals are common, ranging from 1 to 10 cm in length and rarely up to 15 cm. The highest-quality material is in the 1–5 cm range. The crystal faces are normally clean or coated by carbonates and clay minerals.
The purple coloration of amethyst is caused by the presence of an interstitial Fe4+ color center in the quartz (Rossman, 1994), combined with irradiation from natural gamma-ray sources. Irradiation creates color centers that absorb some light wavelengths and produce the very attractive tone seen in this material. The hourglass zoning distinctive of the Boudi mine is created when the iron is incorporated preferentially along the rhombohedral faces. During the growth of the crystal, with the development of the face, the purple sector assumes its typical form.

place in the 2014 AGTA Spectrum Awards, Pairs & Suites. Courtesy of Ai Van Pham
Gem & Gold Creations, Scottsdale, Arizona.

MATERIALS AND METHODS
Gemological properties of 20 faceted amethysts supplied by the Geostone Group were analyzed using standard gem testing instruments. The samples were representative of the material produced from this locality in both their color (light pinkish purple to dark reddish purple) and size range (6.06–17.92 ct).Refractive indices and birefringence values were obtained with a standard refractometer and a near-monochromatic light source. Specific gravity was determined using a Mettler-Toledo hydrostatic meter. Reactions to ultraviolet radiation were observed using standard long-wave (365 nm) and short-wave (254 nm) lamps. Visible absorption spectra were obtained with a Krüss prism spectroscope. Visual features were observed using an SZM-2 zoom microscope from Gemmarum Lapidator with darkfield illumination at 20×–80× magnification. Inclusions were photographed with an Olympus BX41 microscope using immersion techniques.
Chemical composition data were obtained with semi-quantitative, non-destructive EDS microanalysis for determination of major and minor elements. Micro-Raman spectroscopy was used for mineral inclusion identification purposes.
EDS data were acquired at Turin University’s Department of Earth Science using a Cambridge Stereoscan 360 scanning electron microscope, equipped with an Oxford Inca Energy 200 EDS for microanalysis and a Pentafet detector and an ultrathin window for the determination of elements with atomic number down to boron. All spectra were obtained at 15 kV accelerating voltage, 25 mm working distance, and 1 µA probe current for 60 to 300 seconds. Primary standardization was performed on SPI Supplies and Polaron Equipment analytical standards. Daily standardization was performed on a high-purity metallic cobalt standard.
Unoriented micro-Raman spectra were obtained at Turin University with a HoribaJobin Yvon LabRam HRVIS apparatus, equipped with a motorized x-y stage and an Olympus microscope. The backscattered Raman signal was collected with a 50× objective, and the Raman spectrum was obtained for a non-oriented position. The 632.8 nm line of a He-Ne laser was used as the excitation wavelength; laser power was controlled by a series of density filters. The minimum lateral and depth resolution was set to a few µm. The system was calibrated using the 520.6 cm–1 Raman band of silicon before each experimental session. The spectra were collected in 8 to 10 acquisitions with single counting times ranging between 40 and 120 seconds. Spectral manipulation such as baseline adjustment, smoothing, and normalization were performed using the LabSpec 5 software package (HoribaJobin Yvon, 2004 and 2005). For band component analysis, we used the Fityk software package (Wojdyr, 2010), which enabled us to select the type of fitting function and fix or vary specific parameters accordingly. The spectra were recorded for the 100–1300 cm–1 range using the LabSpec 5 program.
RESULTS AND DISCUSSION
The refractive indices of the 20 amethyst samples from Boudi varied from 1.540 to 1.542 (o-ray) and 1.549 to 1.552 (e-ray), with birefringence from 0.009 to 0.010. Pleochroism, observed with a calcite dichroscope, varied from weak to medium bluish purple to reddish purple. None of the samples showed any reaction to either short- or long-wave UV radiation. No absorption spectra were observed using the Krüss spectroscope.



