New 40Ar/39Ar alunite ages from the Colquijirca district, Peru: evidence of a long period of magmatic SO2 degassing during formation of epithermal Au–Ag and Cordilleran polymetallic ores

We present ⁴⁰Ar/³⁹Ar data acquired by infra-red (CO₂) laser step-heating of alunite crystals from the large Miocene Colquijirca district in central Peru. Combined with previously published data, our results show that a long (at least 1.3 My) and complex period of magmatic-hydrothermal activity associated with epithermal Au–(Ag) mineralization and base metal, Cordilleran ores took place at Colquijirca. The new data indicate that incursion of magmatic SO₂-bearing vapor into the Colquijirca epithermal system began at least as early as ∼11.9 Ma and lasted until ∼10.6 Ma. Four alunite samples associated with high-sulfidation epithermal Au–(Ag) ore gave ⁴⁰Ar/³⁹Ar plateau ages between ∼11.9 and ∼11.1 Ma (compared to the previously documented ∼11.6 to ∼11.3 Ma). By combining individually these new ages with crosscutting relationships, the duration of the Au–(Ag) deposition period can be estimated to at least 0.4 My. Three new ⁴⁰Ar/³⁹Ar plateau ages on alunite associated with the base-metal Cordilleran ores are consistent with previously obtained ages, all of them between 10.83 ± 0.06 and 10.56 ± 0.06 Ma, suggesting that most of the sulfide-rich polymetallic deposits of Smelter and Colquijirca formed during this short period. The recognition of consecutive alunite-bearing and alunite-free mineral assemblages within both the Au–(Ag) and the base-metal Cordilleran ores may suggest that SO₂-bearing magmatic vapor entered the epithermal environment as multiple discontinuous pulses, a number of which was not necessarily associated in time with ore fluids. It is likely that a period of SO₂-bearing vapor degassing longer than 11.9 to 10.6 Ma may be recognized with further more detailed work. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Mineral zoning and gold occurrence in the Fortuna skarn mine, Nambija district, Ecuador

The Fortuna oxidized gold skarn deposit is located in the northern part of the Nambija gold district, southern Ecuador. It has been subdivided into four mineralized sites, covering a distance of 1 km, which are named from north to south: Cuerpo 3, Mine 1, Mine 2, and Southern Sector. Massive skarn bodies occur in K–Na metasomatized volcanic and volcaniclastic rocks of the Triassic Piuntza unit. They appear to result from selective replacement of volcaniclastic rocks. Very minor presence of bioclast relicts suggests the presence of subordinate limestone. Endoskarn type alteration with development of Na-rich plagioclase, K-feldspar, epidote, actinolite, anhedral pyroxene, and titanite affects a quartz–diorite porphyritic intrusion which crops out below the skarn bodies in Mine 2 and the Southern Sector. Endoskarn alteration in the intrusion grades into a K-feldspar ± biotite ± magnetite assemblage (K-alteration), suggesting that skarn formation is directly related to the quartz–diorite porphyritic intrusion, the latter being probably emplaced between 141 and 146 Ma. The massive skarn bodies were subdivided into a dominant brown garnet skarn, a distal green pyroxene–epidote skarn, and two quartz-rich varieties, a blue-green garnet skarn and light green pyroxene–garnet skarn, which occur as patches and small bodies within the former skarn types. The proximal massive brown garnet skarn zone is centered on two 060° trending faults in Mine 2, where the highest gold grades (5–10 g/t) were observed. It grades into a distal green pyroxene–epidote skarn zone to the North (Cuerpo 3). Granditic garnet shows iron enrichment from the proximal to the distal zone. Diopsidic pyroxene exhibits iron and manganese enrichment from proximal to distal zones. The retrograde stage is weakly developed and consists mainly of mineral phases filling centimeter-wide veins, vugs, and interstices between garnet and pyroxene grains. The main filling mineral is quartz, followed by K-feldspar, epidote, calcite, and chlorite, with minor sericite, apatite, titanite, hematite, pyrite, chalcopyrite, and gold. Metal and sulfur contents are low at Fortuna, and the highest gold grades coincide with high hematite abundance, which suggests that retrograde stage and gold deposition took place under oxidizing conditions. Fluid inclusions from pyroxene indicate precipitation from high temperature—high to moderate salinity fluids (400 to 460°C and 54- to 13-wt% eq. NaCl), which result probably from boiling of a moderately saline (∼8-wt% eq. NaCl) magmatic fluid. Later cooler (180 to 475°C) and moderate to low saline fluids (1- to 20-wt% eq. NaCl) were trapped in garnet, epidote, and quartz, and are interpreted to be responsible for gold deposition. Chlorite analysis indicates temperature of formation between 300 and 340°C in accordance with fluid inclusion data. It appears, thus, that gold was transported as chloride complexes under oxidizing conditions and was deposited at temperatures around 300°C when transport of chloride complexes as gold carriers is not efficient.     

Provenance-related characteristics of beach sediments around the island of Menorca, Balearic Islands (western Mediterranean)

The island of Menorca, one of the Balearic Islands (Spain) located in the western Mediterranean, is characterised by a contrasting geology and landscape with two major geographic domains: (1) a southern region called Migjorn, comprised of Late Miocene calcarenites and limestones, and (2) a northern region known as Tramuntana, which is composed of folded and faulted Palaeozoic, Mesozoic and Tertiary (Oligocene) siliceous and calcareous rocks. Both domains are lined by numerous pocket beaches exhibiting a high variety of surficial sediment assemblages. Grain-size and compositional analyses revealed that cliff erosion and nearshore Posidonia oceanica meadows are the main sources of sediments consisting mostly of medium- to coarse-grained carbonate sands of marine biogenic origin, with variable amounts of terrigenous rock fragments and quartz. Based on distinctly different contributions of bioclastic material, biogenic carbonates and quartz, 320 sediment samples from 64 beaches were grouped into different facies associations dominated by either (1) biogenic sands, (2) biogenic sands with terrigenous contributions or (3) terrigenous sands with quartz. Nevertheless, there is a marked regional variability in sediment texture and composition. Thus, variable mixtures of carbonate and siliciclastic sediments characterise the beaches of the northern region, whereas the beaches of the southern region are composed mostly of carbonate sands of marine biogenic origin. An exception is the central sector of the south coast, which is enriched in quartz sand (~10 %); this can be related to outcrops of quartz-rich basement rock and also to rocks exposed in some northern drainage basins captured by southern streams since the Plio-Quaternary.     

Two‐hourly surface change on supra‐tidal rock (Marengo,Victoria, Australia)

A traversing micro‐erosion meter was used to measure rock surface micro‐topography over 40 cm² on a supra‐tidal cliff face from early morning to late evening in late spring. From 06:00 hours to 22:00 hours the relative heights of 188 coordinates were obtained using the meter at 2‐hour intervals, resulting in a data set of 1607 readings. Monitoring shows that rock surfaces are dynamic entities, with significant rise and fall relative to the first measurement at shorter timescales than previously reported. The maximum positive rise between readings was 0·261 mm and lowering was 0·126 mm. The pattern of change did not relate as expected to environmental variables such as temperature or insolation. Rather, the surface showed greater surface change in the early morning and late afternoon. It is hypothesized that this pattern relates to the expansion and contraction of lichen thalli as moisture is absorbed during higher humidity in the morning and late afternoon. The implications of these results for weathering studies are considered. Copyright © 2006 John Wiley & Sons, Ltd.