Low-rhenium molybdenite by metamorphism in northern Sweden: Recognition, genesis, and global implications

Re–Os dating of molybdenite is an accurate means to date intrusions and intrusion-related ore deposits using the model age or isochron approach. But, molybdenite has a new niche in the greenschist- to granulite-facies metamorphic environment. Re–Os ages for metamorphic molybdenite may be used to construct regional metamorphic histories. Age significance and accuracy are established by analyzing multiple molybdenite separates extracted from single, petrographically-characterized molybdenite occurrences. In this study, twelve geologically distinct molybdenite-bearing samples from two small Mo districts in northern Sweden trace a 150 m.y. Paleoproterozoic Svecofennian metamorphic history from 1900 to 1750 Ma. These data reveal a little-known, widespread and protracted, Late Svecofennian anatexis in northern Sweden.The Kåtaberget Mo–(Cu, F) deposit is located in the Moskosel granite batholith north of the economically-renown Skellefte district. Four different molybdenite samples from outcrop at Kåtaberget indicate an intrusion age of 1895 ± 6 Ma with the formation of later pegmatite–aplite at 1875 ± 6 Ma. The Allebuoda (Björntjärn) and Munka Mo–(W) deposits in the Rappen district are represented by three outcrop and five drill core samples of molybdenite-bearing aplite–pegmatite–granite. These two deposits were previously described as intrusion-related Climax-type Mo mineralization. Re–Os ages for molybdenites from these deposits range from 1865 to 1750 Ma and, significantly, Re concentrations are markedly low, extending to the sub-ppm level. Age agreement within the deposits is conspicuously lacking, whereas, with one exception, age agreement within any single sample (geologic occurrence), as established by analysis of additional molybdenite separates, is very good. These data, together with fundamental geologic observations discussed in this paper, suggest that Mo–(W) mineralization in northern Sweden is not intrusion-related, but the local product of episodic melting of Archean–Paleoproterozoic supracrustal gneisses related to the Svecofennian orogeny. Petrographic traverses across the boundary between widespread, foliation-parallel units of aplitic to pegmatitic pink granite and hosting biotite gneiss directly capture the process of ore formation. Dehydration breakdown of zircon-rich biotite aligned with the foliation in the gneiss is accompanied by formation of new pristine, post-deformational biotite plus sulfides, oxides, hydrothermal zircon and fluorite, all associated with microcline-dominant leucosomes.This process has profound implication for the traditional leucogranite, intrusion-related genesis attributed to the broad classification of Mo–W–Sn–base and precious metal mineralization (e.g., South Mountain Batholith, Nova Scotia; Okiep, Namaqualand, South Africa; Mactung, Yukon; Pogo–Liese, Tintina, Alaska; Carajás and Goiás–Rio Tocantins, Brazil; New England Batholith, NSW, Australia; Bergslagen, Sweden; Nevoria, Western Australia; Alpeinerscharte, Austria; Erzgebirge, Germany; Sardinia–Corsica Batholith). In addition to biotite, metallogenic contributions (e.g., Mo, W, Sn, U, Bi, Cu, Pb, Zn, Fe, Ni, Co, Au, Ag, Te, As, Sb, REE) in various combinations may also be controlled by breakdown of amphibole. In effect, the trace element composition of dehydrating or recrystallizing components in a gneissic rock essentially defines the local and district metallogenic suite. In the absence of focusing structures (e.g., shear zones, sheeted vein development), this process will generally form small and disconnected subeconomic deposits with erratic and unpredictable grades. Low Re content in associated molybdenite is a key indicator for a subeconomic origin by local melting of biotite gneiss (Mo–W) or muscovite schist (Sn–W).     

Evaluation of the use of photochemical indicators to assess ozone—NOx—VOC sensitivity in the Southwestern Iberian Peninsula

Understanding the chemical links between ozone (O₃) and its two main precursors, nitrogen oxides (NOx) and volatile organic compounds (VOC), is important for designing effective photochemical smog reduction strategies. This chemical relationship will determine which precursor (NOx or VOC) emission reduction will be more effective for decreasing the ozone formation. Under certain conditions, ozone levels decrease as a result of a reduction in NOx emissions but do not respond significantly to changes in VOC emissions (NOx-sensitive condition), while under other conditions ozone concentrations decrease in response to reductions in VOCs and may even increase when NOx emissions are reduced (VOC-sensitive conditions). Indicator species can be used to assess the sensitivity of ozone to changes in the emissions of its precursors. These indicators are species or species ratios involved in ozone photochemistry which reflect the primary chemical process through which the ozone was formed. In this work we use the MM5-CAMx model system to explore the behaviour of various indicator species during two meteorological situations featuring different atmospheric conditions in a complex terrain area. The results show that indicators based on nitrogen compounds (i.e,. NOy and NOz) are suitable for defining the transition range from VOC- to NOx-sensitive chemistry, and that despite the uncertainties associated with the use of chemical indicators, the ratios O₃/NOy and O₃/NOz may provide a simple and useful way to summarize the response of ozone to changes in NOx and VOC emissions in Southwestern Spain.     

Intellectual property rights and low carbon technology transfer: Conflicting discourses of diffusion and development

Intellectual property rights (IPRs) and the transfer of low carbon technologies to developing countries have been the focus of sustained disagreement between many developed and developing country Parties to the United Nations Framework Convention on Climate Change (UNFCCC). We argue that this disagreement stems from two conflicting political discourses of economic development and low carbon technology diffusion which tend to underpin developing and developed countries’ respective motivations for becoming party to the Convention. We illustrate the policy implications of these discourses by examining empirical evidence on IPRs and low carbon technology transfer and highlight how the two discourses are based on an incomplete understanding of the role of technological capacity in either economic development or technology diffusion. This has important implication for the success of post-2012 international climate agreements.     

Propagation of the Storegga tsunami into ice‐free lakes along the southern shores of the Barents Sea

Deposits in coastal lakes in northernmost Norway reveal that the Storegga tsunami propagated well into the Barents Sea ca. 8100–8200 years ago. A tsunami deposit – found in cores from five coastal lakes located near the North Cape in Finnmark – rests on an erosional unconformity and consists of graded sand layers and re‐deposited organic remains. Rip‐up clasts of lake mud, peat and soil suggest strong erosion of the lake floor and neighbouring land. Inundation reached at least 500 m inland and minimum vertical run‐up has been reconstructed to 3–4 m. In this part of the Arctic coastal lakes are usually covered by >1 m of solid lake ice in winter. The significant erosion and deposition of rip‐up clasts indicate that the lakes were ice free and that the ground was probably not frozen. We suggest that the Storegga slide and ensuing tsunami happened sometime in the summer season, between April and October. Copyright © 2011 John Wiley & Sons, Ltd.     

Varve counting reveals high resolution radiocarbon reservoir age variations in palaeolake Lisan

The laminated lacustrine sediments deposited in the last glacial Lake Lisan represent annual deposits of primary aragonite and silty detritus that reflect the annual supply of bicarbonate‐bearing freshwater to the lake. A varve‐counting curve was constructed for the time interval of ca. 17.4–22 cal. ka BP based on aragonite U/Th, and atmospheric radiocarbon ages of organic debris recovered from the studied section. Radiocarbon in the primary (evaporitic) aragonite comprises both atmospheric and old carbon (reflecting the reservoir age). The aragonite reservoir ages were determined by comparing the aragonite radiocarbon dates to the varve counting curve, and are found to lie in the range 1900–600 a and display a continuous decline. This opens the possibility for high (annual) resolution monitoring of the reservoir age, similar in quality to tree ring counting, during the upper part of Marine Isotope Stage (MIS) 2. Our work also demonstrates that a ‘uniform’ reservoir age correction is inappropriate when determining the chronology of short‐term climate events in lacustrine environments. Copyright © 2009 John Wiley & Sons, Ltd.     

Diagenetic effects on the distribution of uranium in live and Holocene corals from the Gulf of Aqaba

We investigated the effects of diagenetic alteration (dissolution, secondary aragonite precipitation and pore filling) on the distribution of U in live and Holocene coral skeletons. For this, we drilled into large Porites lutea coral-heads growing in the Nature Reserve Reef (NRR), northern Gulf of Aqaba, a site close to the Marine Biology Laboratory, Elat, Israel, and sampled the core material and porewater from the drill-hole. In addition, we sampled Holocene corals and beachrock aragonite cements from a pit opened in a reef buried under the laboratory grounds. We measured the concentration and isotopic composition of U in the coral skeletal aragonite, aragonite cements, coral porewater and open NRR and Gulf of Aqaba waters.Uranium concentration in secondary aragonite filling the skeletal pores is significantly higher than in primary biogenic aragonite (17.3 ± 0.6 compared to 11.9 ± 0.3 nmol · g⁻¹, respectively). This concentration difference reflects the closed system incorporation of uranyl tri-carbonate into biogenic aragonite with a U/Ca bulk distribution coefficient (K_D) of unity, versus the open system incorporation into secondary aragonite with K_D of 2.4. The implication of this result is that continuous precipitation of secondary aragonite over ∼1000 yr of reef submergence would reduce the coral porosity by 5% and can produce an apparent lowering of the calculated U/Ca - SST by ∼1°C and apparent age rejuvenation effect of 7%, with no measurable effect on the calculated initial U isotopic composition.All modern and some Holocene corals (with and without aragonite cement) from Elat yielded uniform δ²³⁴U = 144 ± 5, similar to the Gulf of Aqaba and modern ocean values. Elevated δ²³⁴U values of ∼180 were measured only in mid-Holocene corals (∼5000 yr) from the buried reef. The values can reflect the interaction of the coral skeleton with ²³⁴U-enriched ground-seawater that washes the adjacent granitic basement rocks.We conclude that pore filling by secondary aragonite during reef submergence can produce small but measurable effects on the U/Ca thermometry and the U-Th ages. This emphasizes the critical importance of using pristine corals where the original mineralogy and porosity are preserved in paleooceanographic tracing and dating.     

Re–Os molybdenite dating of granite-related Sn–W–Mo mineralisation at Hnilec, Gemeric Superunit, Slovakia

Summary Re–Os molybdenite ages from the exocontact of the Hnilec granite-greisen body provide temporal constraints for tin, tungsten and molybdenite mineralisation in the Gemeric Superunit, Slovakia. Two molybdenite separates were taken from a representative sample of the Sn–W–Mo mineralisation at Hnilec and their Re–Os ages of 262.2 ± 0.9 and 263.8 ± 0.8 Ma (2-sigma) are in excellent agreement. The obtained Re–Os molybdenite ages are similar to recent but less precise electron microprobe monazite (276 ± 13 Ma) and U–Pb single zircon (250 ± 18 Ma) ages from the Hnilec granite intrusion, supporting a granite-related greisen origin for the Sn–W–Mo mineralisation. Our precise Re–Os molybdenite ages resolve the long time controversy over the timing of high-temperature mineralisation in the Gemeric Superunit. These Permian ages eliminate suggestions of an Alpine age. The sulphur isotope composition of the studied molybdenite is δ³⁴S_(CDT) = 1.71 ± 0.2‰ and is consistent with a magmatic sulphur source. Field observations indicate the lack of a broad contact aureole in the vicinity of the Hnilec granite body. Shallow level granite emplacement in schistose host rocks was accompanied by alteration and formation of tin-tungsten greisen in the upper part of the granite and exocontact molybdenite mineralisation, both commonly lacking in other granite bodies within the Gemeric Superunit.     

The geology and Re–Os geochronology of the Palaeoproterozoic Vaikijaur Cu–Au–(Mo) porphyry-style deposit in the Jokkmokk granitoid, northern Sweden

The Vaikijaur Cu–Au–(Mo) deposit is located in the ca. 1.88 Ga calc-alkaline Jokkmokk granitoid near the Archaean–Proterozoic palaeoboundary within the Fennoscandian shield of northern Sweden. The Skellefte VMS district lies immediately to the south and the northern Norrbotten Fe-oxide–Cu–Au deposits to the north. The Vaikijaur deposit occupies an area of 2×3 km within the Jokkmokk granitoid and includes stockwork quartz-sulphide veinlets and disseminated chalcopyrite, pyrite, gold, molybdenite, magnetite, and pyrrhotite. Porphyritic mafic dykes were emplaced along fractures in a ring dyke pattern. The Jokkmokk granitoid, dykes, and the mineralized area are foliated, indicating that mineralization predated the main regional deformation. The mineralized area is characterized by strong potassic alteration. Phyllic and propylitic alteration zones are also present. A pyrite-rich inner core is surrounded by a concentric zone with pyrite, chalcopyrite, and gold. Molybdenite is distributed irregularly throughout the chalcopyrite zone. Geophysical data indicate a strongly conductive central zone in the mineralized area bordered by conductive and high magnetic zones. Five high precision Re–Os age determinations for three molybdenite occurrences from outcrop and drill core samples constrain the age of porphyry-style Cu–Au–(Mo) mineralization to between 1889±10 and 1868±6 Ma. A younger molybdenite is associated with a much later metamorphic event at about 1750 Ma. These data suggest that primary porphyry-style mineralization was associated with calc-alkaline magmatism within the Archaean–Proterozoic boundary zone at ca. 1.89–1.87 Ga.