P–T composition and evolution of paleofluids in the Paleoproterozoic Mag Hill IOCG system,Contact Lake belt,Northwest Territories,Canada

The Echo Bay stratovolcano complex and Contact Lake Belt of the Great Bear Magmatic Zone, Northwest Territories, host a series of coalescing Paleoproterozoic hydrothermal systems that affected an area of several hundred square kilometers. They were caused by intrusion of synvolcanic diorite–monzodioritic plutons into andesitic host rocks, producing several characteristic hydrothermal assemblages. They include early and proximal albite, magnetite–actinolite–apatite, and potassic (K-feldspar) alteration, followed by more distal hematite, phyllic (quartz–sericite–pyrite), and propylitic (chlorite–epidote–carbonate±sericite±albite±quartz) alteration, and finally by late-stage polymetallic epithermal veins. These alteration types are characteristic of iron oxide copper–gold deposits, however, with distal and lower-temperature assemblages similar to porphyry Cu systems. Magnetite–actinolite–apatite alteration formed from high temperature (up to 560 °C) fluids with average salinity of 12.8 wt% NaCl equivalent. The prograde propylitic and phyllic alteration stages are associated with fluids with temperatures varying from 80 to 430 °C and a wide salinity range (0.5–45.6 wt% NaCl equivalent). Similarly, wide fluid temperature (104–450 °C) and salinity (4.2–46.1 wt% NaCl equivalent) ranges are recorded for the phyllic alteration. This was followed by Cu–Ag–U–Zn–Co–Pb sulfarsenide mineralization in late-stage epithermal veins formed at shallow depths and temperatures from 270 °C to as low as 105 °C. The polymetallic veins precipitated from high salinity (mean 30 wt% NaCl equivalent) dense fluids (1.14 g/cm³) with a vapor pressure of 3.8 bars, typical of epithermal conditions. Fluid inclusion evidence indicates that mixed fluids with evolving physicochemical properties were responsible for the formation of the alteration assemblages and mineralization at Mag Hill. An early high temperature, moderate salinity, and magmatic fluid was subsequently modified variably by boiling, mixing with cooler low-salinity meteoric water, and simple cooling. The evidence is consistent with emplacement of the source plutons and stocks into an epithermal environment within ~1 km of surface. This generated near-surface high-temperature alteration in a dynamic hydrothermal system that collapsed (telescoped) resulting in widespread evidence of boiling and epithermal mineralization superimposed on earlier stages of alteration.     

Sorption of uranyl and arsenate on SiO2, Al2O3, TiO2 and FeOOH

Migration of uranium and arsenic in aquatic environments is often controlled by sorption on minerals present along the water flow path. To investigate the sorption behaviour, batch experiments were conducted for uranium and arsenic as single components and also solutions containing both uranium and arsenic in the presence of SiO₂, Al₂O₃, TiO₂ and FeOOH at a pH ranging from 3 to 9. In solutions containing only U(VI) or As(V) with the minerals, the sorption of U(VI) was low at acidic pH range and increases with increasing pH, whereas As(V) showed opposite sorption behaviour to Al₂O₃, TiO₂ and FeOOH from acidic pH range to alkaline condition. For the As(V)–SiO₂ system, the sorption was low for almost all pH. Sorption of U(VI) and As(V) on SiO₂ and FeOOH is almost similar in solutions containing either U(VI) or As(V) separately, or both together. In the U(VI)–As(V)–Al₂O₃ system, a significant retardation in uranyl sorption and an enhancement in arsenate sorption on Al₂O₃ were observed for a wide range of pH. The sorption behaviour of U(VI) and As(V) was changed when Al₂O₃ was replaced by TiO₂, where an increase in sorption was observed for both elements. The sorption behaviour of uranyl and arsenate in the U(VI)–As(V)–TiO₂ system gives evidence for the formation of uranyl–arsenate complexes. The change in sorption retardation/enhancement of U(VI) and As(V) could be explained by the formation of uranyl–arsenate complexes or due to the competitive sorption between uranyl and arsenate species.     

Garnetization as a ground preparation process for copper mineralization: evidence from the Mazraeh skarn deposit, Iran

The Mazraeh Cu–Fe skarn deposit, NW Iran is the result of the intrusion of an Oligocene–Miocene granitic pluton into Cretaceous calcareous rocks. The pluton ranges in composition from monzonite to quartz monzonite, monzogranite, tonalite and granodiorite with I-type, calc-alkaline, and weakly peraluminous characteristics. The Mazraeh pluton was emplaced in a volcanic arc setting in an active continental margin at a depth of ~8 km. Pyroxene skarn, garnet skarn, and epidote skarn zones were formed during the intrusive phase. The garnet skarn developed as exoskarn and endoskarn from the calcareous wall rocks and the pluton, respectively, prior to mineralization. Garnet skarn from the exoskarn zone is identified by relict layering inherited from the precursor calcareous lithologies. Mass balance calculation of garnet skarn in the endoskarn zone indicates that hydrothermal fluids originating from the cooling magma introduced Si, Fe, Mn, Ca, Mg, P, Ag, Cu, Zn, La, Pb, Cd, Mo, and Y. The main mass loss in the garnet skarn was due to destruction of feldspars in the Mazraeh plutonic rocks and leaching of K₂O and Na₂O. Released Ca has been fixed in the andraditic garnet. Garnetization of the Mazraeh pluton was accompanied by mass and volume increase. The magnitude of these changes depends mainly on the degree of alteration and composition of the precursor. The brittle behavior of the endoskarn zone was increased due to formation of massive garnet which subsequently fractured. These fractures not only facilitated movement of hydrothermal fluids but also provided new locations for Cu mineralization. Therefore locating strongly garnetized zones may be a vector to ore in skarn deposits.     

GeoCorpora: building a corpus to test and train microblog geoparsers

In this article, we present the GeoCorpora corpus building framework and software tools as well as a geo-annotated Twitter corpus built with these tools to foster research and development in the areas of microblog/Twitter geoparsing and geographic information retrieval. The developed framework employs crowdsourcing and geovisual analytics to support the construction of large corpora of text in which the mentioned location entities are identified and geolocated to toponyms in existing geographical gazetteers. We describe how the approach has been applied to build a corpus of geo-annotated tweets that will be made freely available to the research community alongside this article to support the evaluation, comparison and training of geoparsers. Additionally, we report lessons learned related to corpus construction for geoparsing as well as insights about the notions of place and natural spatial language that we derive from application of the framework to building this corpus.     

GeoTxt: A scalable geoparsing system for unstructured text geolocation

In this article we present GeoTxt, a scalable geoparsing system for the recognition and geolocation of place names in unstructured text. GeoTxt offers six named entity recognition (NER) algorithms for place name recognition, and utilizes an enterprise search engine for the indexing, ranking, and retrieval of toponyms, enabling scalable geoparsing for streaming text. GeoTxt offers a flexible application programming interface (API), allowing for customized attribute and/or spatial ranking of retrieved toponyms. We evaluate the system on a corpus of manually geo‐annotated tweets. First, we benchmark the performance of the six NERs that GeoTxt provides access to. Second, we assess GeoTxt toponym resolution accuracy incrementally, demonstrating improvements in toponym resolution achieved (or not achieved) by adding specific heuristics and disambiguation methods. Compared to using the GeoNames web service, GeoTxt's toponym resolution demonstrates a 20% accuracy gain. Our results show that places mentioned in the same tweet do not tend to be geographically proximate.     

Vehicle effects on seismic response of a simple‐span bridge during shake tests

Presence of vehicles on a bridge has been observed many times during past earthquakes. Although in practice, the engineers may or may not include the live load contribution to seismic weight in design, current bridge design codes do not specify a certain guideline. A very limited research has been conducted to address this issue from design point of view. The focus of this research is to experimentally assess the effect of a vehicle on the seismic response of a bridge through a large‐scale model. In this scope, a 12‐meter long bridge, having a one lane deck with concrete slab on steel girders, has been shaken under five different ground motions obtained from recent earthquakes that occurred in Turkey, in its transverse direction, both with and without a vehicle on top of the deck. The measured results have indicated that top slab transverse acceleration and bearing displacements can reduce up to 18.7% in presence of a vehicle during seismic tests, which is an indication of reduction in substructure forces. The main reason for the reduction in seismic response of the bridge in the presence of live load can be ascribed to the increase in damping of the system due to mass damper‐like action induced by the vehicle. This beneficial effect cannot be observed in vertical seismic response. Copyright © 2014 John Wiley & Sons, Ltd.     

Hydrothermal alteration and mineralisation of the Glen Eden Mo-W-Sn deposit: a leucogranite-related hydrothermal system,Southern New England Orogen,NSW, Australia

The Glen Eden Mo-Sn-W deposit in north-eastern New South Wales, Australia, is an example of a leucogranite-related, low-grade, large-tonnage hydrothermal system. It occurs in the southern part of the New England Orogen and is hosted within Permian felsic volcanic rocks, intruded at depth by dykes of porphyritic microleucogranite (Glen Eden Granite). The deposit is hosted within a pipe-like quartz-rich greisen breccia body about 500 m in diameter, surrounded by a greisen zone several hundred metres across, zoning out into altered volcanic rocks. The dominant ore minerals, largely hosted as open space fillings and disseminations in quartz and quartz-rich greisen, are molybdenite, wolframite and cassiterite; they are accompanied by minor to trace amounts of muscovite, fluorite, topaz, siderite, pyrrhotite, arsenopyrite, chalcopyrite, sphalerite, bismuth, bismuthinite, joseite A, cosalite, galenobismutite, beryl, anatase and late-stage dickite and kaolinite. Two types of breccia are recognised: (1) greisenised volcanic rock fragments (quartz + muscovite), cemented by hydrothermal quartz ± K-feldspar ± ore minerals, and (2) fragments of hydrothermal quartz ± cassiterite ± wolframite enclosed in quartz ± clay. In both types of breccia and in stockwork veins, there is evidence of early precipitation of Mo-Sn-W phases, followed by Bi minerals and base metal sulfides (± fluorite, siderite).Breccia formation and associated hydrothermal alteration (greisen, potassic, argillic, propylitic) are interpreted to be related to devolatilisation of the highly fractionated Glen Eden Granite of early Triassic age (240±1 Ma based on ⁴⁰Ar/³⁹Ar geochronology of greisen muscovite) as well as to fluid mixing with meteoric waters. The breccia pipe could have formed in part by rock dissolution and collapse, as well as by explosive degassing of boiling fluids. Fluid inclusion evidence is consistent with boiling, with breccia pipe formation and mineralisation having mainly occurred at 250–350 °C from fluids with salinity of 0.4–9 wt% NaCl equivalent in the dilute types and 30–47 wt% NaCl equivalent in the hypersaline types. Stable isotopic evidence (O, D, C, S) indicates a strong magmatic contribution to the hydrothermal fluids and metals in the breccia. The ¹⁸O values of quartz decrease outward from the breccia pipe (10.6–12.3 in the pipe to 3.4–8.7 in the peripheral quartz) indicating that there has been mixing with isotopically light (high latitude) meteoric fluids, mainly after formation of the breccia pipe.     

Geology and geochemistry of the Mendejin plutonicrocks, Mianeh, Iran

The Mendejin pluton is located in the Mianeh area, NW Iran, 550 km from Tehran. This pluton is probably of Oligo-Miocene age and is the result of extensive magmatism which occurred during and after the Alpine Orogeny. Similar plutons are common in the Alborz–Azarbaijan structural zone of Iran, and it is likely that there are concealed plutons related to this extensive Cenozoic magmatism, but due to their youth and low rates of erosion they have not yet been exposed. The Mendejin pluton is a composite body made up of four types of plutonic rocks: pink tonalite, grey tonalite, diorite and aplite. The pink tonalite is porphyritic and contains phenocrysts of plagioclase, K-feldspar and hornblende in a groundmass consisting of quartz, plagioclase, K-feldspar, hornblende, zircon, monazite, leucoxene, apatite and hematite. The grey porphyritic tonalite has more biotite, pyroxene and pyrite and less accessory phases compared with the pink tonalite. The diorite has a microporphyritic texture with phenocrysts of plagioclase, hornblende and augite. This rock also occurs as xenoliths in the Mendejin pluton. The aplitic dykes are the youngest magmatic products at Mendejin. The Mendejin tonalite contains more Cl, As, S, Cu, Ni and Zn than the global granite. These rocks are of I-type, peraluminous and calc-alkaline, with medium to high potassium, and were formed as part of a volcanic arc. The Mendejin pluton contains up to 8 ppb gold and could potentially have been the source of an economic gold deposit by leaching of Au from wall rocks and deposition in extensive hydrothermally altered marginal zones.