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Castelnuovo Mine (Castelnuovo Pit; Castelnuovo deposit), Cavriglia, Arezzo Province, Tuscany, Italyi
Regional Level Types
Castelnuovo Mine (Castelnuovo Pit; Castelnuovo deposit)Open-Cast Mine (Reclaimed)
CavrigliaCommune
Arezzo ProvinceProvince
TuscanyRegion
Italy- not defined -

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Latitude & Longitude (WGS84):
43° 32' 40'' North , 11° 27' 50'' East
Latitude & Longitude (decimal):
Type:
Open-Cast Mine (Reclaimed) - last checked 2020
Köppen climate type:
Nearest Settlements:
PlacePopulationDistance
Castelnuovo dei Sabbioni1,242 (2014)1.0km
Neri678 (2014)1.2km
Massa158 (2014)1.7km
Meleto639 (2014)2.7km
San Cipriano-S.Barbara-Centinale1,977 (2014)3.1km
Mindat Locality ID:
21094
Long-form identifier:
mindat:1:2:21094:7
GUID (UUID V4):
b9aeb43d-484b-4a95-b49b-a478f25b2005
Other Languages:
Italian:
Miniera Castelnuovo (Cavo minerario Castelnuovo; Giacimento Castelnuovo), Cavriglia, Provincia di Arezzo, Toscana, Italia


Open-pit mine of the Santa Barbara mining concession, situated near the village of Castelnuovo dei Sabbioni, opened in the homonymous lignite deposit in the period 1956-1994. It reached the depth of 150 m. Presently reclaimed.

The first mine, opened in 1864 in the Castelnuovo deposit, was an open-pit mine named Casino mine (Miniera del Casino). Later, the deposit was mined mainly by underground methods and included various mines such as the mines named Castelnuovo or Bicchierone, Cave Vecchie, Poggio d'Avene, Le Culle, Carpinete, Basi, and Valle al Pero. Castelnuovo's last underground mine, Carpinete (43.553163 N, 11.473551 E), closed in 1969.

The first mineral described for this lignite deposit is a white-yellowish fossil resin, found as small brittle blades, often grouped to form fibrous-radiating spherules, and incrustations in lignite. It was supposed a new species and named bombiccite (Bechi, 1868; Bombicci, 1869; and other authors). Studies performed by Boeris (1921) and Ciusa & Galizzi (1921) led to suppose the possible sameness between bombiccite and hartite, later confirmed by X-ray powder diffraction and single-crystal analyses performed by Pellizzer (1955 a,b). Detailed work concerning the hartite structure was subsequently published by Foresti Serantoni et al. (1978), who established this natural diterpene as having the alpha-dihydrophyllocladene structure.

Other minerals reported in the first period of mining activity are siderite and pyrite. Siderite was first noted by Grattarola (1876) as small crystals in lignite fissures. According to Sagri & Magi (1992), it can be found, both within Meleto Clays and the lignite layers, as lenses and nodules, and rarely as yellowish-brown euhedral microcrystals. Pyrite was found as small crystalline masses during the underground mining operations in stopes characterised by gaseous exhalation (Castelli, 1922).

The recent mining operations allowed to discover layered deposits of phosphates inside the Meleto Clays. Anapaite and vivianite were abundantly found, but always separately in different layers.
In particular, anapaite appears as radiating masses with variable shape and size. The interior contains many cavities filled by aggregates of triclinic tabular crystals. The crystals are green or yellow-green, translucent, vitreous, and a millimeter or two in size. A gradual change in the character of the masses, with regard to their position inside Meleto Clays, has been observed: in the uppermost part there are small nodules, nearly spherical and about 1 cm in diameter, progressing to nodules as large as 10 cm in diameter in the lower part. The anapaite nodules often appear joined together to form a compound cluster. At the bottom of the formation of Meleto Clays, near the Macigno Sandstone, layers of anapaite with a thickness ranging from 5 to 20 cm and an extension of tens of meters occur. Anapaite is rarely associated with baryte, as thin, radiating, hemispherical, yellowish aggregates no larger than 1 mm.
Vivianite most commonly occurs as a replacement of vegetable organic matter; blue to dark blue, perfectly preserved leaves have been collected in a bluish clayly matrix. The concretionary radiating nodules are also very attractive; they are blue, up to 7 cm in size and have cavities lined with bright blue vivianite crystals to 2 mm. Blue earthy concretions also occur.

Castelnuovo mine, is the type locality for grattarolaite and rodolicoite, two anhydrous iron phosphates, found as reddish-brown nodules in lignite beds which appear to have naturally burned. The two mineral species occur as small crystallites (<100 nm), associated in fine-scale intergrowth that prevent the measurement of physical properties.

Gypsum, as aggregates of greyish dull prismatic crystals, has been occasionally found in the bluish clays. However, the best specimens, consisting of colourless elongated crystals reaching several centimetres in length, have been found on a particular orange-red brick-like matrix, which formed during lignite self-combustion through clay baking and the consequent oxidation of ferrous minerals (Billi, 1980; Brizzi et al., 1991; Corazza et al., 1994).

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Standard Detailed Gallery Strunz Chemical Elements

Mineral List


12 valid minerals. 2 (TL) - type locality of valid minerals.

Rock Types Recorded

Note: data is currently VERY limited. Please bear with us while we work towards adding this information!

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Alphabetical List Tree Diagram

Detailed Mineral List:

Anapaite
Formula: Ca2Fe2+(PO4)2 · 4H2O
References:
Baryte
Formula: BaSO4
Branchite
Formula: C20H34
References:
Grattarolaite (TL)
Formula: Fe3+3(PO4)O3
Type Locality:
Gypsum
Formula: CaSO4 · 2H2O
Hematite
Formula: Fe2O3
Description: as blackish, thin layers hosted by roasted clays; some hematite has a velvety texture produced by layers of microcrystals.
Maghemite
Formula: (Fe3+0.670.33)Fe3+2O4
Description: as massive brown specimens distinguished by a strong magnetic susceptibility.
Pyrite
Formula: FeS2
Rodolicoite (TL)
Formula: Fe3+PO4
Type Locality:
Siderite
Formula: FeCO3
References:
Sulphur
Formula: S8
Description: very rarely occurs as thin crusts and small masses associated with gypsum on an orange-red brick-like matrix, which formed during lignite self-combustion through clay baking and the consequent oxidation of ferrous minerals.
Vivianite
Formula: Fe2+Fe2+2(PO4)2 · 8H2O
References:

Gallery:

Ca2Fe2+(PO4)2 · 4H2O Anapaite
Fe2+Fe2+2(PO4)2 · 8H2O Vivianite

List of minerals arranged by Strunz 10th Edition classification

Group 1 - Elements
Sulphur1.CC.05S8
Group 2 - Sulphides and Sulfosalts
Pyrite2.EB.05aFeS2
Group 4 - Oxides and Hydroxides
Maghemite4.BB.15(Fe3+0.670.33)Fe3+2O4
Hematite4.CB.05Fe2O3
Group 5 - Nitrates and Carbonates
Siderite5.AB.05FeCO3
Group 7 - Sulphates, Chromates, Molybdates and Tungstates
Baryte7.AD.35BaSO4
Gypsum7.CD.40CaSO4 · 2H2O
Group 8 - Phosphates, Arsenates and Vanadates
Rodolicoite (TL)8.AB.Fe3+PO4
Grattarolaite (TL)8.BE.10Fe3+3(PO4)O3
Vivianite8.CE.40Fe2+Fe2+2(PO4)2 · 8H2O
Anapaite8.CH.10Ca2Fe2+(PO4)2 · 4H2O
Group 10 - Organic Compounds
Branchite10.BA.10C20H34

List of minerals for each chemical element

HHydrogen
H AnapaiteCa2Fe2+(PO4)2 · 4H2O
H GypsumCaSO4 · 2H2O
H VivianiteFe2+Fe22+(PO4)2 · 8H2O
H BranchiteC20H34
CCarbon
C SideriteFeCO3
C BranchiteC20H34
OOxygen
O AnapaiteCa2Fe2+(PO4)2 · 4H2O
O BaryteBaSO4
O GypsumCaSO4 · 2H2O
O HematiteFe2O3
O Maghemite(Fe3+0.670.33)Fe23+O4
O SideriteFeCO3
O VivianiteFe2+Fe22+(PO4)2 · 8H2O
O GrattarolaiteFe33+(PO4)O3
O RodolicoiteFe3+PO4
PPhosphorus
P AnapaiteCa2Fe2+(PO4)2 · 4H2O
P VivianiteFe2+Fe22+(PO4)2 · 8H2O
P GrattarolaiteFe33+(PO4)O3
P RodolicoiteFe3+PO4
SSulfur
S BaryteBaSO4
S GypsumCaSO4 · 2H2O
S PyriteFeS2
S SulphurS8
CaCalcium
Ca AnapaiteCa2Fe2+(PO4)2 · 4H2O
Ca GypsumCaSO4 · 2H2O
FeIron
Fe AnapaiteCa2Fe2+(PO4)2 · 4H2O
Fe HematiteFe2O3
Fe Maghemite(Fe3+0.670.33)Fe23+O4
Fe PyriteFeS2
Fe SideriteFeCO3
Fe VivianiteFe2+Fe22+(PO4)2 · 8H2O
Fe GrattarolaiteFe33+(PO4)O3
Fe RodolicoiteFe3+PO4
BaBarium
Ba BaryteBaSO4

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