Chemical composition of rock-forming minerals in gold-related granitoid intrusions,southwestern New Brunswick,Canada: implications for crystallization conditions,volatile exsolution,and fluorine-chlorine activity

Chemical composition of rock-forming minerals in Appalachian Siluro-Devonian granitoid intrusions, southwestern New Brunswick, was systematically determined by electron microprobe. The mineral chemical data together with petrographic examination was used to test magmatic equilibration and to constrain crystallization conditions, volatile exsolution, and fluorine-chlorine activity of fluids associated with these intrusions. Mineralogical distinction between Late Silurian to Early Devonian granodioritic to monzogranitic series (GMS) and Late Devonian granitic series (GS) rocks is evident, although both are subsolvus I-type to evolved I-type granitoids. Oxidized to reduced GMS rocks consist of quartz, plagioclase (An>10), K-feldspar, biotite, apatite, titanite, zircon, monazite, ± hornblende, ± pyroxene, ± magnetite, ± ilmenite, and ± sulfide. GS rocks comprise quartz, K-feldspar, plagioclase (An<10), mica group minerals, zircon, monazite, apatite, sulfide, ± ilmente, ± magnetite, ± topaz, ± columbite, and ± xenotime. Inter-intrusion and intra-intrusion variations in mineral chemistry are interpreted to reflect petrogenetic processes (e.g., assimilation and fractional crystallization) during granitoid evolution. Although magmatic equilibration among rock-forming minerals are disturbed by subsolidus hydrothermal processes, GMS rocks appear to have higher magmatic temperatures, variable levels of emplacement, a range of (i.e., reduced intrusions 10^−16.7∼10^−13.4 and oxidized intrusions 10^−14.0∼10^−10.5 bars), and relatively low f _HF/f _HCl ratios (10^−3.0∼10^−1.0) in exsolved fluids, compared to GS rocks. Reduced GMS intrusions bear higher gold potential and thus may be prospective targets for intrusion-related gold systems. Electronic Supplementary Material Supplementary material is available for this article at     

Refining the timing of eclogite metamorphism: a geochemical,petrological, Sm-Nd and U-Pb case study from the Pohorje Mountains,Slovenia (Eastern Alps)

High-pressure metamorphism in the Pohorje Mountains of Slovenia (Austroalpine unit, Eastern Alps) affected N-MORB type metabasic and metapelitic lithologies. Thermodynamic calculations and equilibrium phase diagrams of kyanite–phengite-bearing eclogites reveal PT conditions of >2.1 GPa at T<750°C, but within the stability field of quartz. Metapelitic eclogite country rocks contain the assemblage garnet + phengite + kyanite + quartz, for which calculated peak pressure conditions are in good agreement with results obtained from eclogite samples. The eclogites contain a single population of spherical zircon with a low Th/U ratio. Combined constraints on the age of metamorphism come from U/Pb zircon as well as garnet–whole rock and mineral–mineral Sm-Nd analyses from eclogites. A coherent cluster of single zircon analyses yields a ²⁰⁶Pb/²³⁸U age of 90.7±1.0 Ma that is in good agreement with results from Sm-Nd garnet–whole rock regression of 90.7±3.9 and 90.1±2.0 Ma (εNd: +8) for two eclogite samples. The agreement between U-Pb and Sm-Nd age data strongly suggests an age of approximately 90 Ma for the pressure peak of the eclogites in the Pohorje Mountains. The presence of garnet, omphacite and quartz inclusions in unfractured zircon indicates high-pressure rather than ultrahigh pressure conditions. The analysed metapelite sample yields a Sm-Nd garnet–whole rock scatterchron age of 97±15 Ma. These data probably support a single P-T loop for mafic and pelitic lithologies of the Pohorje area and a late Cretaceous high-pressure event that affected the entire easternmost Austroalpine basement including the Koralpe and Saualpe eclogite type locality in the course of the complex collision of the Apulian microplate and Europe.     

A Mössbauer study of pseudotachylytes: redox conditions during seismogenic faulting

The redox conditions during frictional melting provide information on the physical and chemical conditions during seismic slip in the crust. Here we examine frictional melts from five localities by analyzing host rocks and corresponding pseudotachylytes using Mössbauer spectroscopy. The faults examined are located at South Mountain, Arizona; Fort Foster, Maine (two localities); Long Ridge fault, North Carolina; and the Homestake shear zone, Colorado. The main iron-bearing phases in the pseudotachylytes are phyllosilicates (biotite, muscovite and clays) and iron oxides (magnetite and hematite) and minor pyrite. The ferrous/ferric ratios of the phyllosilicates in the host rocks are the same as those in the pseudotachylytes, except for the hematite-bearing pseudotachylyte from the Long Ridge fault, which is more oxidized. The magnetites in the host rocks and the corresponding pseudotachylytes have different ferric and ferrous iron distributions, which is attributed to different cation chemistry, rather than redox conditions. With the exception of the South Mountain locality, the ferric/ferrous ratios of the micas are interpreted to record the primary redox state of the pseudotachylyte melt as the calculated oxygen fugacities are consistent with magnetite and hematite equilibria. Pyrite-bearing pseudotachylytes plot ~0–1 log₁₀ units above the fayalite-magnetite-quartz (FMQ) buffer. Magnetite-bearing pseudotachylytes plot ~2–4 log₁₀ units above the FMQ buffer, and hematite-bearing pseudotachylytes plot 3.5 log₁₀ units above the hematite-magnetite (HM) buffer. Hematite-bearing pseudotachylytes, together with previous oxygen isotope data, are inferred to represent melting in the presence of externally derived pressurized water. Other localities are inferred to represent melting under rock-buffered, closed system, conditions. If the localities studied are representative of seismogenic faulting, the calculated oxygen fugacities indicate that, in the system C–O–H–S, H₂O and CO₂ should be the dominant fluid species. This is the first detailed study of the redox state of pseudotachylytes.     

Contrasting interactions of sodium and potassium with H<Subscript>2</Subscript>O in haplogranitic liquids and glasses at 200 MPa from hydration–diffusion experiments

This study examines hydration–diffusion in the metaluminous haplogranite system at 200 MPa H₂O and 800–300°C. At 800°C hydration is accompanied by melting and uphill diffusion of sodium from anhydrous glass toward the region of hydration and melting, whereas potassium diffuses away from the hydration front and into anhydrous glass. Silicon and aluminum are simply diluted upon hydration. There is no change in molecular Al/(Na + K) throughout the entire hydration-diffusion aureole and, therefore, (1) there is no loss of alkalis to the vapor, and (2) K migrates to replace Na in order to maintain local charge balance required by ^IVAl. Alkali diffusion occurs over a viscosity contrast from 10^4.1 Pa s in hydrous liquid to 10^11.8–10^13.5 Pa s in anhydrous glass. From these results, we interpret that: (1) Na is structurally or energetically favored over K as a charge-balancing cation for ^IVAl in hydrous granitic liquids, whereas the opposite behavior has been observed for anhydrous melts, and (2) the diffusion of alkalis through silicate melts is largely independent of viscosity. Results from 600°C are similar to those at 800°C, but hydration at 300°C involves a loss of Na and concomitant increase in molar Al/(Na + K) in the hydration zone due to hydrogen-alkali exchange between fluid and glass. Hydration behavior at 400°C is transitional between those at 300°C and 600°C, suggesting that the change in hydration mechanism occurs near the glass transition.     

Glassy orthopyroxene granodiorites of the Pannonian Basin: tracers of ultra-high-temperature deep-crustal anatexis triggered by Tertiary basaltic volcanism

Glassy orthopyroxene granodiorite-tonalite (named pincinite after type locality) was described from basaltic lapilli tuffs of the Pliocene maar near Pinciná village in the Slovakian part of the Pannonian Basin. Two pincinite types exhibit a qualitatively similar mineral composition (quartz, An_20–55 plagioclase, intergranular silicic glass with orthopyroxene and ilmenite, ±K-feldspar), but strongly different redox potential and formation PT conditions. Peraluminous pincinite is reduced (6–7% of total iron as Fe³⁺ in corundum-normative intergranular dacitic glass) and contains ilmenite with 8–10 mol% Fe₂O₃ and orthopyroxene dominated by ferrosilite. High-density (up to 0.85 g/cm³) primary CO₂ inclusions with minor H₂, CH₄, H₂S, CO and N₂ (<2 mol% total) are present in Qtz and Plg. Equilibrium PT conditions inferred from the intergranular Opx–Ilm–Glass assemblage and fluid density correspond to 1,170±50°C, 5.6±0.4 kbar, respectively. Metaluminous pincinite is more oxidised (25–27% of total iron as Fe³⁺ in diopside-normative intergranular glass of rhyolite–trachyte–dacite composition) and contains Fe₂O₃-rich ilmenite (17–29 mol%) associated with enstatite. Fluid inclusions are composed of CO₂–H₂O mixtures with up to 38 mol% H₂O. Raman spectroscopy revealed H₂S along with dominant CO₂ in the carbonic phase. Equilibrium PT parameters for the intergranular Opx–Ilm–Glass assemblage correspond to 740±15°C, 2.8±0.1 kbar, respectively. Reducing gas species (<2 mol% total) in the CO₂-inclusions of the peraluminous pincinite resulted from hydrogen diffusion due to fH₂ gradient imposed during decrease of redox potential from the log fO₂ values near QFM during Qtz + Plg growth, to QFM-2 incidental to the superimposed Opx + Ilm assemblage in the intergranular melt. The decrease in oxygen fugacity was recorded also in the metaluminous pincinite, where log fO₂ values changed from ~QFM + 2.6 to QFM + 0.4, but hydrogen diffusion did not occur. Absence of OH-bearing minerals, major and trace element abundances (e.g. REE 300–320, Nb 55–57, Th 4–31, Zr 240–300 ppm, FeO_tot/MgO up to 11), and Sr–O isotope ratios in the pincinites are diagnostic of high-temperature anorogenic magmas originated by dehydration melting of biotite in quartz-feldspathoid crust (⁸⁷Sr/⁸⁶Sr>0.705–0.706, ¹⁸O>9 V-SMOW) around alkali basalt reservoir in depths between 17 and 20 km, and around late stage derivatives of the basalt fractionation, intruding the crust up to depths of 10–11 km. Low water activity in the pincinite parental melt was caused by CO₂-flux from the Tertiary basaltic reservoirs and intrusions. The anatexis leads to generation of a melt-depleted granulitic crust beneath the Pannonian Basin, and the pincinites are interpreted as equivalents of igneous charnockites and enderbites quenched at temperatures above solidus and unaffected by sub-solidus re-equilibration and metamorphic overprint.     

Experimental and geochemical evidence for derivation of the El Capitan Granite,California, by partial melting of hydrous gabbroic lower crust

Partial melting of mafic intrusions recently emplaced into the lower crust can produce voluminous silicic magmas with isotopic ratios similar to their mafic sources. Low-temperature (825 and 850°C) partial melts synthesized at 700 MPa in biotite-hornblende gabbros from the central Sierra Nevada batholith (Sisson et al. in Contrib Mineral Petrol 148:635–661, 2005) have major-element and modeled trace-element (REE, Rb, Ba, Sr, Th, U) compositions matching those of the Cretaceous El Capitan Granite, a prominent granite and silicic granodiorite pluton in the central part of the Sierra Nevada batholith (Yosemite, CA, USA) locally mingled with coeval, isotopically similar quartz diorite through gabbro intrusions (Ratajeski et al. in Geol Soc Am Bull 113:1486–1502, 2001). These results are evidence that the El Capitan Granite, and perhaps similar intrusions in the Sierra Nevada batholith with lithospheric-mantle-like isotopic values, were extracted from LILE-enriched, hydrous (hornblende-bearing) gabbroic rocks in the Sierran lower crust. Granitic partial melts derived by this process may also be silicic end members for mixing events leading to large-volume intermediate composition Sierran plutons such as the Cretaceous Lamarck Granodiorite. Voluminous gabbroic residues of partial melting may be lost to the mantle by their conversion to garnet-pyroxene assemblages during batholithic magmatic crustal thickening.     

Clay mineralogical,geochemical and isotopic tracing of the evolution of the Woodleigh impact structure,Southern Carnarvon Basin,Western Australia

Chaotically structured diamictite from the inner ring syncline surrounding the central uplift of the Woodleigh impact structure contains shocked metamorphic and impact melt-rock fragments, largely derived from Ordovician and Devonian target sandstones. Coarse illite fractions (<2 m) from the sandstones containing no K-feldspar yield K–Ar ages of around 400 Ma, whereas the K–Ar ages of authigenic clays of >0.2 m fractions from the diamictite without smectite and K-feldspar cluster around 360 Ma, consistent with Rb–Sr data. Crystallisation of newly formed illite in the impact melt rock clasts and recrystallisation of earlier formed illite in the sandstone clasts preserved in the diamictite, are attributed to impact-induced hydrothermal processes in the Late Devonian. The illitic clays from the diamictite and from the sandstones have very similar trace element compositions, with significantly enriched incompatible lithophile elements, which increase in concentrations correlatively with those of the compatible ferromagnesian elements. The unusual trace element associations in the clays may be due to the involvement of hot gravity-driven basinal fluids that interacted with rocks of the Precambrian craton to the east of the study area, or with such material transported and reworked in the studied sedimentary succession.     

Value of Climate Forecasts for Adjusting Farming Strategies in Sub-Saharan Africa

Sustaining and increasing crop production and productivity has to be a major policy thrust for developing countries. Using a simulation approach different production strategies were evaluated conditioned on climate information to derive optimal strategies to help farmers reduce risk and increase productivity. By examining the existence of options in this case planting dates the study provides an analyses of the expected value and risks associated with changing decisions based on the availability of climate forecasts. The 15-March planting date produced the highest mean yield for the two cultivars examined although 1-April, 15-April and 1-May plantings had one to zero probability of crop failures compared to 15-March with crop failures in 4 out of 20 years. Results indicate losses of between 25 and 35 kg/day due to delays in planting from 15-March planting to 1-June planting for the 120- and 150-day cultivar. El niño years were associated with positive yield deviations for both cultivars and most planting dates. Farmers are known to make tactical adjustments to their management in light of information perceived relevant to the prospects of forthcoming crop. Although in its present form most current forecast products do not provide information on onset of the rainfall, however the information they do provide could play a crucial role in helping farmers reduce the risks posed by climatic variability.     

Development and the Household: Missing the point?

Over the past two decades development has been shifting its focus toward smaller scales and particular problems. As a result, the household has become an increasingly important institution for development, and has come under increased scrunity as development practitioners and scholars seek to better understand this institution’s functions and foundations, trying to ‘get the household right’. These efforts, rather than clarifying the character and the function of the household, have contributed to its indeterminacy by reifying the very institution they seek to analyse. Arguing that these efforts fundamentally miss the point of examining the household, this paper introduces a different framework of analysis that addresses the household not as a fixed object of research, but as a local construction that embodies flows of power and knowledge both within and transcending the local. Using the example of varying constructions of the household in two villages in Ghana’s Central Region, this article illustrates how such an approach allows us to address the various functions of the household as particular embodiments of these flows, an approach that better explains the endurance or ephemerality of these functions. Such an approach provides a stronger foundation for the consideration of how particular constructions of this institution may have troubling implications for issues like gender equity and sustainability.     

Vulnerability,Partnerships and the Pursuit of Survival: Urban Livelihoods and Apprenticeship Contracts in a West African City

This paper analyses local level apprenticeship contracts and networks to highlight informal urban livelihoods within the context of socio-economic vulnerability and wider contemporary changes taking place in Koforidua, Ghana. It does so by specifically examining the complex entanglements of interpersonal relationships that characterize apprenticeship contracts within which home-based entrepreneurs and artisans in Koforidua engage in to sustain both current livelihoods, as well as to shore themselves against socio-economic vulnerability triggered in part by adjustment. As a result of the changing geography of the city, network entanglements, comprising resilient ties and egalitarian relations, have become vital to urban livelihoods in this community. However, apprenticeship contracts and the networks they engender can be a double-edged sword. For instance, demands of reciprocity or support from co-network members, neighbours and family, can be so taxing that some individuals opt out of the network. This tension notwithstanding, this paper contends that apprenticeship contracts and the network spaces they create have created a new social cohesion and community that transcend the traditionally known spaces of social support, i.e. ethnic ties, family ties or even institutional support.