Regional-scale Proterozoic IOCG-mineralized breccia systems: examples from the Wernecke Mountains, Yukon, Canada

A large scale Proterozoic breccia system consisting of numerous individual breccia bodies, collectively known as Wernecke Breccia, occurs in north-central Yukon Territory, Canada. Breccias cut Early Proterozoic Wernecke Supergroup sedimentary rocks and occur throughout the approximately 13 km thick deformed and weakly metamorphosed sequence. Iron oxide–copper–gold ± uranium ± cobalt mineralization is associated with the breccia bodies and occurs as veins and disseminations within breccia and surrounding rocks and locally forms the breccia matrix. Extensive sodic and potassic metasomatic alteration occurs within and around breccia bodies and is overprinted by pervasive calcite and dolomite/ankerite, and locally siderite, alteration, respectively. Multiple phases of brecciation, alteration and mineralization are evident. Breccia bodies are spatially associated with regional-scale faults and breccia emplacement made use of pre-existing crustal weaknesses and permeable zones. New evidence indicates the presence of metaevaporitic rocks in lower WSG that may be intimately related to breccia formation. No evidence of breccia-age magmatism has been found to date.

Constructing quality: The multinational histories of chocolate

Geographic research on food quality, while considering many of the ways in which quality is socially constructed, has largely focused on the place-based aspects of the raw materials of food production. Here, we use French convention theory to look at a highly processed food in order to show how place associations in the social construction of food quality extend to manufacturing. For chocolate, quality is based on material characteristics whose relative importance in determining quality depends on the country in which different stages of economic innovation took place. Struggles over the definition of quality chocolate, as exemplified by the “European Chocolate War,” show how quality issues are connected to geographies of manufacturing and innovation.     

(Re-)negotiating access: The politics of researching skills and knowledge for ‘sustainable communities’

The last decade has witnessed a surge of interest in ‘sustainable communities’ within the UK. This has stimulated a plethora of research aimed at acquiring a better understanding of what ‘sustainable communities’ might look like and how they can be achieved. However, this has not been accompanied by a reflection and interrogation of the actual processes, challenges and politics of doing ‘sustainable communities’ research. This paper addresses this gap by highlighting the importance of paying attention to the on-going process of negotiating access when carrying out sustainability research at the community level. We draw on a recent study of skills and knowledge for ‘sustainable communities’ in Stroud Gloucestershire, UK, to illustrate the importance of sensitivity to social relationships throughout and beyond the research trajectory within sustainability research. Our experience raises important questions about the politics of research practices when doing sustainability research ‘with’ communities and the challenges associated with participatory approaches as a means to demonstrate research impact. We argue that in developing a fuller understanding of why and how different types of community level initiatives can contribute to the ‘sustainable communities’ agenda, greater consideration needs to be given to how these community practices can be better supported through the process of doing academic research.     

Variability of laboratory procedures and results in geoarchaeology

Many laboratory techniques are available to geoarchaeologists to determine physical or chemical attributes of sediment or soil samples, and several techniques are often available for analysis of a single attribute. This is illustrated by analyzing duplicate sediment and soil samples from the British Camp Site (Washington) and Lubbock Lake Site (Texas) using two methods for organic carbon content, two methods for organic matter content, and three methods for calcium carbonate content, and several pretreatment procedures for particle-size analysis. These comparisons illustrate that different methods of analysis for the same property of duplicate samples can yield different results. Therefore, when making comparisons with data from other sites or other investigators, the types of laboratory methods used in geoarchaeological analyses are important considerations. Choice of a particular technique will depend on a variety of factors, often conflicting, including the archaeological and geoarchaeological questions being asked, the physical and chemical nature of the samples, and the accuracy, efficiency, and cost of the method.     

H<Subscript>2</Subscript>O solubility in basalt at upper mantle conditions

This study presents a new experimental approach for determining H₂O solubility in basaltic melt at upper mantle conditions. Traditional solubility experiments are limited to pressures of ~600 MPa or less because it is difficult to reliably quench silicate melts containing greater than ~10 wt% dissolved H₂O. To overcome this limitation, our approach relies on the use of secondary ion mass spectrometry to measure the concentration of H dissolved in olivine and on using the measured H in olivine as a proxy for the concentration of H₂O in the co-existing basaltic melt. The solubility of H₂O in the melt is determined by performing a series of experiments at a single pressure and temperature with increasing amounts of liquid H₂O added to each charge. The point at which the concentration of H in the olivine first becomes independent of the amount of initial H₂O content of the charge (added + adsorbed H₂O) indicates its solubility in the melt. Experiments were conducted by packing basalt powder into a capsule fabricated from San Carlos olivine, which was then pressure-sealed inside a Ni outer capsule. Our experimental results indicate that at 1000 MPa and 1200 °C, the solubility of H₂O in basaltic melt is 20.6 ± 0.9 wt% (2 × standard deviation). This concentration is considerably higher than predicted by most solubility models but defines a linear relationship between H₂O fugacity and the square of molar H₂O solubility when combined with solubility data from lower pressure experiments. Further, our solubility determination agrees with melting point depression determined experimentally by Grove et al. (2006) for the H₂O-saturated peridotite solidus at 1000 MPa. Melting point depression calculations were used to estimate H₂O solubility in basalt along the experimentally determined H₂O-saturated peridotite solidus. The results suggest that a linear relationship between H₂O fugacity and the square of molar solubility exists up to ~1300 MPa, where there is an inflection point and solubility begins to increase less strongly with increasing H₂O fugacity.     

Nitrogen Mass Fraction and Stable Isotope Ratios for Fourteen Geological Reference Materials: Evaluating the Applicability of Elemental Analyser Versus Sealed Tube Combustion Methods

Thirteen commercially available silicate reference materials (RM) and one in‐house reference material, eleven of which have no previously published values, were analysed for nitrogen mass fraction and isotopic ratios with an Elemental Analyser (EA), and a Sealed Tube Combustion line, coupled to a continuous flow isotope ratio mass spectrometer (IRMS). These materials ranged from < 10 μg g^?1 to 1% m/m nitrogen mass fractions and δ¹⁵N of ?0.5 to +19.8‰. Existing nitrogen RM BHVO‐2, MS#5 and SGR‐1b were used to assess the accuracy of the data from the sealed tube combustion line, which was found to be in good agreement with existing published values. In contrast, the EA‐IRMS failed to fully liberate nitrogen from all silicate rocks and minerals (achieving a mean of 44 ± 10% nitrogen yield) resulting in kinetic fractionation of isotope values by ?1.4‰ on average. Therefore, sealed tube combustion is better suited for analyses of silicate‐bound nitrogen. The EA worked reliably for organic samples, but care should be taken when using the EA for silicate nitrogen research. Moving forward, it is recommended that BHVO‐2, Biotite‐Fe, FK‐N and UB‐N be used as quality control materials as they appear to be most reproducible in terms of nitrogen mass fraction (relative error < 10%, 1s), and isotopic composition (< 0.6‰, 1s).     

Mountain hazards and the resilience of social–ecological systems: lessons learned in India and Canada

Mountain regions are subject to a variety of hazardous processes. Earthquakes, landslides, snow avalanches, floods, debris flows, epidemics and fires, among other processes, have caused injury, death, damage and destruction. They also face challenges from increased populations, and expansion and intensification of␣activities, land uses and infrastructure. The combination of a dynamic bio- geophysical environment and intensified human use has increased the vulnerability of mountain social–ecological systems to risk from hazards. The ability of social–ecological systems to build resilience in the context of hazards is an important factor in their long-term sustainability. The role of resilience building in understanding the impact of hazards in mountain areas is examined and illustrated, in part, through examples from Canada and India. Resilient social–ecological systems have the ability to learn and adjust, use all forms of knowledge, to self-organize and to develop positive institutional linkages with other social–ecological systems in the face of hazards. The analysis suggests that traditional social–ecological systems built resilience through avoidance, which was effective for localized hazards. The more recent development and implementation of cross-scale institutional linkages is shown to be a particularly effective means of resilience building in mountain social–ecological systems in the face of all hazards.     

Faecal-indicator bacteria and sedimentary processes in estuarine mudflats (Seine, France)

Over a three-year period, quantification of faecal indicators and the molecular detection of Escherichia coli and Salmonella were monitored in sediments from three contrasting mudflats of the Seine estuary (France). The elevation of the mudflat surface was monitored concurrently using a high-resolution altimeter. During the period of the study, estuarine mudflats were areas of deposition for faecal-indicator bacteria and were mainly controlled by sedimentary processes. In the intertidal freshwater and subtidal mudflats, the highest abundances of faecal-indicator bacteria were counted during a depositional period. Maximum levels were observed in the freshwater mudflats during periods of high flow: thermotolerant coliforms: 3.9 x 10(4) cfu cm(-2), enterococci: 1.2 x 10(4) cfu cm(-2), Clostridium perfringens spores: 9.8 x 10(5) spores cm(-2). Loss of culturability of enteric bacteria in sediment microcosms demonstrated the remediatory capacity of the mudflats, even if they might be a secondary source of bacteria-forming spores to the water column through erosion and resuspension events.     

Ancient geochemical cycling in the Earth as inferred from Fe isotope studies of banded iron formations from the Transvaal Craton

Variations in the isotopic composition of Fe in Late Archean to Early Proterozoic Banded Iron Formations (BIFs) from the Transvaal Supergroup, South Africa, span nearly the entire range yet measured on Earth, from –2.5 to +1.0‰ in ⁵⁶Fe/⁵⁴Fe ratios relative to the bulk Earth. With a current state-of-the-art precision of ±0.05‰ for the ⁵⁶Fe/⁵⁴Fe ratio, this range is 70 times analytical error, demonstrating that significant Fe isotope variations can be preserved in ancient rocks. Significant variation in Fe isotope compositions of rocks and minerals appears to be restricted to chemically precipitated sediments, and the range measured for BIFs stands in marked contrast to the isotopic homogeneity of igneous rocks, which have δ⁵⁶Fe=0.00±0.05‰, as well as the majority of modern loess, aerosols, riverine loads, marine sediments, and Proterozoic shales. The Fe isotope compositions of hematite, magnetite, Fe carbonate, and pyrite measured in BIFs appears to reflect a combination of (1) mineral-specific equilibrium isotope fractionation, (2) variations in the isotope compositions of the fluids from which they were precipitated, and (3) the effects of metabolic processing of Fe by bacteria. For minerals that may have been in isotopic equilibrium during initial precipitation or early diagenesis, the relative order of δ⁵⁶Fe values appears to decrease in the order magnetite > siderite > ankerite, similar to that estimated from spectroscopic data, although the measured isotopic differences are much smaller than those predicted at low temperature. In combination with on-going experimental determinations of equilibrium Fe isotope fractionation factors, the data for BIF minerals place additional constraints on the equilibrium Fe isotope fractionation factors for the system Fe(III)–Fe(II)–hematite–magnetite–Fe carbonate. δ⁵⁶Fe values for pyrite are the lowest yet measured for natural minerals, and stand in marked contrast to the high δ⁵⁶Fe values that are predicted from spectroscopic data. Some samples contain hematite and magnetite and have positive δ⁵⁶Fe values; these seem best explained through production of high ⁵⁶Fe/⁵⁴Fe reservoirs by photosynthetic Fe oxidation. It is not yet clear if the low δ⁵⁶Fe values measured for some oxides, as well as Fe carbonates, reflect biologic processes, or inorganic precipitation from low-δ⁵⁶Fe ferrous-Fe-rich fluids. However, the present results demonstrate the great potential for Fe isotopes in tracing the geochemical cycling of Fe, and highlight the need for an extensive experimental program for determining equilibrium Fe isotope fractionation factors for minerals and fluids that are pertinent to sedimentary environments.