Irish-type deposits comprise carbonate-hosted sphalerite- and galena-rich lenses concentrated near normal faults. We present new data from the Tara Deep resource and overlying mineralization, at Navan, and the Island Pod deposit and associated Main zone orebodies, at Lisheen. Tara Deep mineralization predominantly replaces Tournasian micrites and subordinate Visean sedimentary breccias. The mineralization is mainly composed of sphalerite, galena, marcasite and pyrite. A range of Cu- and Sb-bearing minerals occur as minor phases. At Tara Deep, paragenetically early sulfides exhibit negative δ34S values, with later phases displaying positive δ34S values, indicating both bacterial sulfate reduction (BSR) and hydrothermal sulfur sources, respectively. However, maximum δ34S values are heavier (25‰) than in the Main Navan orebody (17‰). These mineralogical and isotopic features suggest that Tara Deep represents near-feeder mineralization relative to the Navan Main orebody. The subeconomic mineralization hosted in the overlying Thin Bedded Unit (TBU) comprises sphalerite replacing framboidal pyrite, both exhibiting negative δ34S values (−37.4 to −8.3‰). These features indicate a BSR source of sulfur for TBU mineralization, which may represent seafloor exhalation of mineralizing fluids that formed the Tara Deep orebody. The Island Pod orebody, at Lisheen, shows a mineralogical paragenetic sequence and δ34S values broadly similar to other Lisheen orebodies. However, the lack of minor Cu, Ni, and Sb minerals suggests a setting more distal to hydrothermal metal feeder zones than the other Lisheen orebodies. Pb isotope data indicate a very homogeneous Lower Palaeozoic Pb source for all Navan orebodies. Lower Palaeozoic metal sources are also inferred for Lisheen, but with variations both within and between orebodies. Carbon and oxygen isotopic variations at Navan and Lisheen appear to result from fluid-carbonate rock buffering. The emerging spectrum of mineralogical and isotopic variations define proximal to distal characteristics of Irish-type systems and will assist in developing geochemical vectoring tools for exploration.

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The Palaeoproterozoic Kerry Road deposit is one of the oldest examples of volcanogenic massive sulfide (VMS) mineralization. This small VMS deposit (~500,000 tons grading at 1.2% Cu, 3.5% Zn) is hosted in amphibolite facies mafic-siliciclastic units of the c. 2.0 Ga Loch Maree Group, Scotland. Sulfide mineralization consists of pyrite and pyrrhotite with subordinate chalcopyrite and sphalerite, occurring in disseminated, vein and semi-massive to massive textures.The deposit was highly deformed and metamorphosed during the c. 1.8-1.7 Ga Laxfordian Orogeny. Textural relationships of deformed sulfide minerals, related to early Laxfordian deformation (D1/D2), indicate initial high pressure-low temperature (100 MPa, 150ºC) conditions before reaching peak amphibolite facies metamorphism, as evident from pyrrhotite crossing the brittle/ductile transition prior to chalcopyrite. Late Laxfordian deformation (D3/D4) is marked by local retrograde greenschist facies at low pressure and temperature (<1.2MPa, <200°C), recorded by late red sphalerite remobilization. 34 S values from all sulfide minerals have a homogeneous mean of 0.8 ± 0.7 ‰ (n=21), consistent with interaction of hydrothermal fluids in the host oceanic basalt-island arc setting envisaged for deposition of the Loch Maree Group.Microprobe analyses of amphiboles record evidence of the original alteration halo associated with the Kerry Road deposit, with a systematic Mg-and Si-enrichment from ferrotschermakite (~150 m) to Mg-hornblende (~90 m) to actinolite (0 m) on approach to the VMS deposit. Furthermore, whole rock geochemistry records a progressive enrichment in Si, Cu, Co, and S, and depletion in Al, Ti, V, Cr, Y and Zr with proximity to the VMS system. These elemental trends, together with amphibole geochemistry, are potentially useful 3 exploration vectors to VMS mineralization in the Loch Maree Group, and in similar highly deformed and metamorphosed terranes elsewhere.

Cobalt in the Congolese Copperbelt mines is commonly recovered from Co-oxi-hydroxides (i.e. heterogenite, asbolane) by acid-leaching under reducing conditions. However, most operations face a limit in the leaching yields of cobalt, which usually do not exceed 80%. The main aim of this work was to investigate the causes of the poor recovery, in order to reconcile the Co recovery with processing techniques. Several concentrate samples from different mine plants of Katanga Copperbelt (Kalukuluku, Mutanda, Mabaya, Kamwali and Fungurume) were selected and subjected to a full mineralogical characterisation by Optical Microscopy (OM), X-Ray Diffraction (XRD), automated mineralogy and Scanning Electron Microscopy by Energy Dispersive Spectroscopy (SEM-EDS) prior and after leaching tests. OM and XRD results were used as background information to build a mineral list for mineral identification during automated mineralogy analyses by Mineralogic Mining System (Zeiss ltd.). Automated mineralogy allowed obtaining mineral maps, modal mineralogy, chemical assays and Co deportment for each specimen prior and after leaching. Mineral maps of the leached samples were useful to observe the occurrences of poorly leached Co-bearing particles which were further investigated by SEM-EDS and X-mapping. The results showed that heterogenite (rarely associated with asbolane) is the main cobalt mineral in Katanga. Mineralogic Mining System was able to discriminate between pure heterogenite, and Si-Al-K-bearing heterogenite, asbolane/heterogenite, Heterogenite+Fe-oxi-hydroxide and Co-bearing mixed phases, which resulted more refractory to leaching. The comparison between modal mineralogy of pre-and post-leached samples indicates a decrease, but not a full leaching of these Co phases: chemical assays and Codeportment, in fact, still reveal the presence of low Co% within Co phases listed above (Table 1). SEM-EDS and Xmapping on single particles of some specimens corroborated the results obtained by Mineralogic.