Textural variation in the pyrite-rich ore deposits of the Røros district, Trondheim Region, Norway: implications for pyrite deformation mechanisms

The Røros district is a pyrite-rich polymetallic sulfide orefield in the southeastern part of the Trondheim region, Central Norwegian Caledonides. All of the ore deposits at Røros are hosted within a Cambrian to Silurian succession that was deformed and metamorphosed at lower greenschist to lower amphibolite facies conditions during the Caledonian orogeny. Samples from five individual deposits across the orefield have been analyzed using a combination of reflected light petrographic observation, orientation contrast imaging, and electron backscatter diffraction. Results indicate that, whereas samples from each ore deposit have a variety of different textures, all of them preserve plastic deformation in pyrite grains that occurred at peak metamorphic conditions characterized by the development of internal lattice misorientation within pyrite grains and low-angle (～2°) dislocation walls. These observations indicate that the principal deformation mechanisms at peak metamorphic conditions were dislocation glide and creep. The preservation of brittle fracturing represents later overprinting events.     

Temporally varying ethylene emission on Jupiter

Ethylene (C₂H₄) emission has been measured in the poles and equator of Jupiter. The 949 cm⁻¹ spectra were recorded with a high resolution spectrometer at the McMath-Pierce telescope at Kitt Peak in October-November 1998 and at the Infrared Telescope Facility at Mauna Kea in June 2000. C₂H₄ is an important product of methane chemistry in the outer planets. Knowledge of its abundance can help discriminate among the various proposed sets of CH₄ photolysis branching ratios at Ly-α, and determine the relative importance of the reaction pathways that produce C₂H₂ and C₂H₆. In the equatorial region the C₂H₄ emission is weak, and we were only able to detect it at high air-mass, near the limb. We derive a peak equatorial molar abundance of C₂H₄ of 4.5×¹⁰⁻⁷-1.7×¹⁰⁻⁶ near 2.2×¹⁰⁻³ mbar, with a total column of 5.7×¹⁰¹⁴-2.2×¹⁰¹⁵ molecules cm⁻² above 10 mbar depending upon choice of thermal profile. We observed enhanced C₂H₄ emission from the poles in the regions where auroras are seen in X-ray, UV, and near infrared images. In 2000 we measured a short-term change in the distribution of polar C₂H₄ emission; the emission in the north IR auroral “hot spot” decreased by a factor of three over a two-day interval. This transient behavior and the sensitivity of C₂H₄ emission to temperature changes near its contribution peak at 5-10 microbar suggests that the polar enhancement is primarily a thermal effect coupled with vertical transport. Comparing our observations from Kitt Peak and Mauna Kea shows that the C₂H₄ emission of the northern non-“hot spot” auroral regions did not change over the three-year period while that in the southern polar regions decreased.     

Cupriferous bogs in the Sackville area, New Brunswick, Canada

Two cupriferous bogs in the Sackville area of New Brunswick, Canada, are described. The organic matter (muck) in these bogs contains from 2 to 6% Cu, derived from cupriferous springs that carry copper in amounts ranging from 0.005 to 1 ppm. The source of the copper in the springs is unknown, but the metal probably originates from the leaching of cupriferous (chalcocitic) deposits in grits and conglomerates at the base of the Boss Point Formation of Carboniferous (Pennsylvanian) age.The copper occurs in the muck as copper humate(s), the precise chemical characterization of which is unknown.Examples of copper bogs related to copper mineralization in many parts of the world are reviewed, and it is pointed out that such bogs are good geochemical indicators of cupriferous deposits.The moss, Pohlia nutans, grows in the springs in the copper bogs and in other wet sites in the area where large concentrations of copper occur. This moss is tolerant to large amounts of available copper and markedly accumulates the metal. When slightly chlorotic Pohlia nutans may indicate the presence of higher than normal amounts of copper.     

The impacts of pyroclastic surges on buildings at the eruption of the Soufrière Hills volcano, Montserrat

We investigated the impacts on buildings of three pyroclastic surges that struck three separate villages on 25 June, 21 September and 26 December, 1997, during the course of the andesitic dome building eruption of the Soufrière Hills Volcano, Montserrat, which began on 18 July, 1995. A detailed analysis of the building damage of the 26 December event was used to compare the findings on the flow and behaviour of dilute pyroclastic density currents (PDCs) with the classical reports of PDCs from historical eruptions of similar size. The main characteristics of the PDC, as inferred from the building damage, were the lateral loading and directionality of the current; the impacts corresponded to the dynamic pressure of the PDC, with a relatively slow rate of rise and without the peak overpressure or a shock front associated with explosive blast; and the entrainment of missiles and ground materials which greatly added to the destructiveness of the PDC. The high temperature of the ash, causing the rapid ignition of furniture and other combustibles, was a major cause of damage even where the dynamic pressure was low at the periphery of the current. The vulnerability of buildings lay in the openings, mainly windows, which allowed the current to enter the building envelope, and in the flammable contents, as well as the lack of resistance to the intense heat and dynamic pressure of some types of vernacular building construction, such as wooden chattel houses, rubble masonry walls and galvanised steel-sheet roofs. Marked variability in the level of damage due to dynamic pressure (in a range 1–5 kPa, or more) was evident throughout most of the impact area, except for the zone of total loss, and this was attributable to the effects of topography and sheltering, and projectiles, and probably localised variations in current velocity and density. A marked velocity gradient existed from the outer part to the central axis of the PDC, where buildings and vegetation were razed to the ground. The gradient correlated with the impacts due to lateral loading and heat transfer, as well as the size of the projectiles, whilst the temperature of the ash in the undiluted PDC was probably uniform across the impact area. The main hazard characteristics of the PDCs were very consistent with those described by other authors in the classic eruptions of Pelée (1902), Lamington (1951) and St Helens (1980), despite differences in the eruptive styles and scales. We devised for the first time a building damage scale for dynamic pressure which can be used in research and in future volcanic emergencies for modelling PDCs and making informed judgements on their potential impacts. Editorial responsibility: T. Druitt     

The use of major elemental ratios in detailed geochemical prospecting utilizing primary halos

The behaviour of the ratios K₂O/Na₂O, SiO₂/CO₂, and $\text{SiO}{}_2\text{H}{}_2\text{O}\text{+ CO}{}_2\text{+ S}$ in the alteration envelopes of a variety of epigenetic deposits is documented. It is concluded that the ratio K₂O/Na₂O is the most suitable for estimating proximity to ore during exploration drilling programs. The other two ratios are useful in indicating proximity to ore only under certain geological conditions. Before the use of ratios is contemplated in detailed exploration programs within a given mineral belt orientation studies should be carried out to determine the trend of the ratios with proximity to mineralization.     

Iron, manganese, and lead at Hawaii Ocean Time-series station ALOHA: Temporal variability and an intermediate water hydrothermal plume

Trace metal clean techniques were used to sample Hawaii Ocean Time-series (HOT) station ALOHA on seven occasions between November 1998 and October 2002. On three occasions, full water-column profile samples were obtained; on the other four occasions, surface and near-surface euphotic zone profiles were obtained. Together with three other published samplings, this site may have been monitored for “dissolved” (≤0.4 or ≤0.2 μm) Fe more frequently than any other open ocean site in the world.Low Fe concentrations (<0.1 nmol kg⁻¹) are seen in the lower euphotic zone, and Fe concentrations increase to a maximum in intermediate waters. In the deepwaters (>2500 m), the concentrations we observe (0.4-0.5 nmol kg⁻¹) are significantly lower than some other deep North Pacific stations but are similar to values that have been reported for a station 350 miles to the northeast. We attribute these low deepwater values to transport of low-Fe Antarctic Bottom Water into the basin and a balance between Fe regeneration and scavenging in the deep water. Near-surface waters have higher Fe levels than observed in the lower euphotic zone. Significant temporal variability is seen in near-surface Fe concentrations (ranging from 0.2-0.7 nmol kg⁻¹); we attribute these surface Fe fluctuations to variable dust deposition, biological uptake, and changes in the mixed layer depth. This variability could occur only if the surface layer Fe residence time is less than a few years, and based on that constraint, it appears that a higher percentage of the total Fe must be released from North Pacific aerosols compared to North Atlantic aerosols. Surprisingly, significant temporal variability and high particulate Fe concentrations are observed for intermediate waters (1000-1500 m). These features are seen in the depth interval where high δ³He from the nearby Loihi Seamount hydrothermal fields has been observed; the total Fe/³He ratio implies that the hydrothermal vents are the source of the high and variable Fe.The vertical profile of Mn at ALOHA qualitatively resembles other North Pacific Mn profiles with surface and intermediate water maxima, but there are some significant quantitative differences from other reported profiles. The ≤0.4 μm Mn concentration is highest near the surface, decreases sharply in the upper 500 m, then shows an intermediate water maximum at 800 m and then decreases in the deepest waters; these concentrations are higher than observed at a station 350 miles to the northeast that shows similar vertical variations. It appears that there is a significant Mn gradient (throughout the water column) from HOT towards the northeast.Compared to the first valid oceanic Pb data for samples collected in 1976, Pb at ALOHA in 1997-1999 shows decreases in surface waters and waters shallower than 200 m. Pb concentrations in central North Pacific surface waters have decreased by a factor of 2 during the past 25 yr (from ∼65 to ∼30 pmol kg⁻¹); surface water Pb concentrations in the central North Atlantic and central North Pacific are now comparable. We attribute the surface water Pb decrease to the elimination of leaded gasoline in Japan and to some extent by the U.S. and Canada. We attribute most of the remaining Pb in Pacific surface waters to Asian emissions, more likely due to high-temperature industrial activities such as coal burning rather than to leaded gasoline consumption. A 3-year mixed-layer time series from the nearby HALE-ALOHA mooring site (1997-1999) shows that there is an annual cycle in Pb with concentrations ∼20% higher in winter months; this rise may be created by downward mixing of the winter mixed layer into the steep gradient of higher Pb in the upper thermocline (Pb concentrations double between the surface and 200 m). From 200 m to the bottom, Pb concentrations decrease to levels of 5-9 pmol kg⁻¹ near the bottom; for most of the water column, thermocline and deepwater Pb concentrations do not appear to have changed significantly during the 23-yr interval.