Kalungaite, PdAsSe, is a new mineral discovered in the Buraco do Ouro gold mine, Cavalcante town, Goiás State, Brazil. It occurs in a quartz-muscovite mylonite, related to a peraluminous granite, in platy anhedral aggregates along foliation planes. Associated ore minerals are gold, chalcopyrite, bohdanowiczite, an unnamed Pb-Bi-Se-S mineral, clausthalite, guanajuatite, stibiopalladinite, sperrylite and padmaite. Gangue minerals are muscovite, quartz and rare tourmaline and magnetite. Kalungaite is lead-grey, has a metallic lustre, a black streak and is brittle with uneven fracture. No cleavage was observed. The mineral has a micro-indentation hardness of VHN25 = 438 (range of 429–455 kg/mm2 from five indentations). Under reflected light, kalungaite is cream, or creamy grey adjacent to gold grains, has no internal reflections and is isotropic. Reflectance values in air (and in oil) are: 47.5 (33.3) at 470 nm, 46.9 (32.6) at 546 nm, 46.8 (32.6) at 589 nm and 48.0 (34.0) at 650 nm. The average of eight electron-microprobe analyses gives: Pd 41.32, As 27.49, Bi 0.35, Sb 1.59, Se 27.67 and S 1.22, total 99.64 wt. %, corresponding to Pd1.006(As0.950Sb0.034Bi0.004)Σ0.988(Se0.908S0.099)Σ1.007Kalungaite is cubic, space group Pa, a = 6.089(4) Å, V = 225.78 Å3, Z = 4. Dcalc is 7.59 g/cm3. The strongest seven X-ray powder-diffraction lines [d in Å(I)(hkl )] are: 3.027(75)(002), 1.838(100)(113), 1.172(95)(115, 333), 1.077(80)(044, 144, 334), 0.988(70)(116, 235, 253), 0.929(90)(335) and 0.918(70)(226). Kalungaite is interpreted as having formed from hydrothermal fluids of granitic origin, during syn-emplacement shearing and alteration, producing an unusual gold-platinum-group element deposit.

In the Pontal auriferous lode, dominant saccharoidal quartz is associated with oligoclase, biotite, hornblende, tremolite-actinolite, sulphides (less than 2%), and disseminated native gold. Four main types of fluid inclusion have been distinguished based on their habit, distribution and spatial relation-ship with gold particles. Type S are primary multiphase large sized (100 to 200 µm) inclusions with homogenization temperatures (V + L → L) between 350 and 450°C. They contain siderite and/or calcite and graphite-like microcrystals as daughter phases. Commonly associated with these inclusions are tiny (50 to 100 µm) solid inclusions of biotite or actinolite. In most of these inclusions, only CH4 has been detected in the vapour phase. However some noticeable exceptions were observed (CO2/CH4 ratio near 0.85). Type C inclusions are later than gold and occur disseminated in quartz or along trails that crosscut quartz grain boundaries. They may contain nahcolite daughter crystals. CO2/CH4 ratios range from 0.0 to 0.5. Homogenization temperatures vary from 150 to 300°C. Type V are mainly gaseous CH4-H2O inclusions. They may occur as small-sized inclusions directly associated with gold particles. Type L are aqueous two-phase inclusions of late secondary origin.

The scattering of the CO2/CH4 ratios could be related to fluctuations of the oxygen fugacity that triggered gold precipitation at the time of trapping. These variations of fO2 with time could reflect unbuffered fluid-rock interaction with respect to redox conditions during quartz deposition.

Finally, gold deposition is interpreted to have occurred at elevated temperature (500°C) and pressure, compatible with boundary conditions between greenschist and amphibolites facies.

An unworked quartz vein-hosted gold deposit occurs in the Clew bay area of County Mayo, western Ireland. The veins are late-Caledonian in age and transect greenschist-facies poly-deformed Silurian quartzites. The veins contain disseminated arsenopyrite that may be a primary mineral source for elevated levels of arsenic (As) found in groundwater samples recovered from wells related spatially to the gold deposit. Levels from 5 to 188 μg/L (significantly above the 7.5 μg/L threshold for safe drinking water) have been detected. A series of element distribution maps using a scanning electron microscope (Hitachi model S-4700) linked to an energy-dispersive spectrometer (INCA® Oxford Instruments) and mineral distribution maps generated by QEMSCAN® (Quantitative Evaluation of Minerals by Scanning electron microscopy) were used to map the distribution of the primary arsenopyrite and related secondary As-bearing phases. Laser Raman microspectroscopy was used to identify the secondary As-bearing phases. 'Island weathering' of primary arsenopyrite together with hydrated pseudomorphs of arseniosiderite, pharmacosiderite and scorodite after arsenopyrite are recorded. Circulating groundwater hydrates the primary arsenopyrite, providing the release mechanism that forms the secondary As-bearing phases that occur as microfracture infills together with muscovite and biotite. The textural relationships between the primary and secondary As minerals indicate their potential as mineral sources of As that could enter transport pathways leading to its release into groundwater.