The Colors of the Circus Mosaic from Barcino (Roman Barcelona): Characterization, Provenance, and Technology Issues

Archaeometric studies on mosaics often concentrate only on glass tesserae, while comprehensive studies including both stone and glass tesserae are scarce; however, both types of tesserae can sometimes bring relevant data to elaborate archaeological knowledge on a studied mosaic. In this paper, a representative set of tesserae from a large polychrome Roman mosaic retrieved in Barcelona (NE Spain) is investigated using various methods. Most of the techniques were directly applied on samples prepared as petrographic thin sections (including polarized-light, cathodoluminescence and electron microscopies, and synchrotron through-the-substrate μX-ray diffraction). The results indicate that, from the ten sampled stone tesserae, there are (i) seven limestones, one of them identified as Alveolina limestone (early Eocene) from the southern Pyrenees (ii) two sandstones from Barcelona’s Montjuïc hill (Miocene) and, (iii) a Carrara white marble from the Apuan Alps (Italy). The profuse presence of tesserae of both local and imported materials with well-known uses in architecture, epigraphy, and sculpture could imply that tesserae were a by-product of their main use. Two different production technologies were identified for the three sampled glass tesserae. The concurrent use of antimony- and tin-based opacifiers is in agreement with the accepted archaeological chronology of the mosaic (4th century AD).

Innovative Approaches for the Sedimentological Characterization of Fine Natural and Anthropogenic Sediments in Karst Systems: The Case of the Apuan Alps (Central Italy)

The Apuan Alps (NW Tuscany) is an important area of Central Italy characterized by large karst systems mainly fed via direct and diffuse water infiltration (autogenic recharge). These waters usually transport a clastic sediment load, originated by natural, surface and subsurface rock erosion/weathering which, in part, is deposited underground. In the Apuan Alps, during extreme rain event, huge amounts of carbonate powder, produced as a waste resulting from the quarrying operations of the famous “Carrara” marble, mix up with meteoric waters forming a slurry that is transported through the karst openings into the caves, where the carbonate powder may be deposited along with natural sediments. Depending upon karst hydrology and water fluxes, the slurry may eventually reach karst springs heavily reducing water quality. Mineralogical composition of the sediments collected along karst waterways and springs shows variable proportions of calcite associated with dolomite and silicates particles whereas the marble powder samples from quarry areas are mainly composed by calcite grains. Cave deposits of natural origin have usually a fine-sand grain size whereas spring sediments have a more variable grain-size distribution. Marble powder mainly has a silt grain size and produces a sort of “granulometric and morphometric pollution” which influences the transport mechanism of solid load through the karst systems along both vadose and phreatic waterways.

Secondary Sulfates from the Monte Arsiccio Mine (Apuan Alps, Tuscany, Italy): Trace-Element Budget and Role in the Formation of Acid Mine Drainage

A suite of sulfate minerals from the Monte Arsiccio mine (Apuan Alps, Northern Tuscany, Italy), previously identified by using both X-ray diffraction and micro-Raman spectroscopy, was studied through inductively coupled plasma mass spectrometry (ICP-MS), in order to determine their trace-element content. Several elements (Tl, Rb, As, Sb, Co, Ni, Cu, Zn, and Cr) were found above the detection limits. Among them, some are important from an environmental perspective and may reach relatively high concentrations (e.g., Tl = 1370–2988 μg/g; As = 505–1680 μg/g). Thus, these sulfates may act as transient sinks for some of these potentially toxic elements, as well as for sulfate ions and acidity. Indeed, dissolution experiments revealed the ability of these secondary minerals to produce a significant pH decrease of the solutions, as well as the release of Fe, Al, and K as major ions. This work discusses the relation between the budget of trace elements and the crystal chemistry of sulfate minerals and provides new insights about the environmental role played by the sulfate dissolution in controlling the quality of water in acid mine drainage systems.

Sulfates from the Pyrite Ore Deposits of the Apuan Alps (Tuscany, Italy): A Review

The occurrence of sulfate minerals associated with the pyrite ores of the southern Apuan Alps has been known since the 19th century but modern mineralogical studies started only in the last decade. Sulfate assemblages were identified in all the pyrite ore deposits from the studied area but the more impressive associations were discovered in the Fornovolasco and Monte Arsiccio mines. Their study allowed to improve the knowledge of the sulfate crystal-chemistry and to achieve a better understanding of the acid mine drainage (AMD) systems associated with pyrite oxidation. More than 20 different mineral species were identified and, among them, four sulfates (volaschioite, giacovazzoite, magnanelliite, and scordariite) have their type localities in the pyrite ore deposits of the Apuan Alps. A review of the mineralogical results of a ten-year-long study is given here.

Crystal-chemistry of micas belonging to the yangzhumingite-fluorophlogopite and phlogopite-fluorophlogopite series from the Apuan Alps (northern Tuscany, Italy)

The present work reports the crystal-chemical characterization of micas from the Monte Arsiccio and Buca della Vena mines (Apuan Alps, Italy) through electron microprobe analysis, single-crystal X-ray diffraction, and Raman spectroscopy. The sample from the Monte Arsiccio mine can be classified as an intermediate member of the yangzhumingite-fluorophlogopite series, with average crystal-chemical formula (K0.85Na0.01Ba0.09)Σ=0.95(Mg2.11Fe2+0.23Fe3+0.11Cr3+0.01Al0.20Ti0.04☐0.30)Σ=3.00(Si3.20Al0.80)Σ=4.00O10.00F1.90Cl0.02(OH)0.08. Unit-cell parameters are a ~ 5.30, b ~ 9.18, c ~ 10.14 Å, β ~ 100.12°, V ~ 486.22 Å3, corresponding to the 1M polytype. Structure refinements, performed in C2/m space group, converged to R1 = 3.54 and 4.46% and provided Mg plus Fe occupancy in the range 86–94% for the octahedral M1 and M2 sites. Raman spectroscopy shows very weak bands in the OH stretching region at ~ 3690 and 3580 cm−1. The sample from the Buca della Vena mine has been identified as an (OH)-rich fluorophlogopite, with average crystal-chemical formula (K0.84Na0.02Ca0.01)Σ=0.87(Mg2.12Fe2+0.55Fe3+0.10Al0.18☐0.05)Σ=3.00(Si2.99Al1.01)Σ=4.00O10.00F1.02Cl0.09(OH)0.89. Its unit-cell parameters are a ~ 5.33, b ~ 9.22, c ~ 10.23 Å, β ~ 100.09°, V ~ 494.39 Å3. Structure refinements gave good R1 values (3.27 and 4.37%) and revealed octahedral occupancy of 82–84% Mg and 16–18% Fe. Strong Raman signals at ~ 3702 cm−1 and 3595 cm−1 were observed in the OH stretching region. The findings allow to better understand not only the mineralogy of the Apuan Alps but, more generally, the crystal chemical details of intermediate dioctahedral-trioctahedral mica belonging to the yanzhumingite-fluorophlogopite series.