Olivine in the Udachnaya-East Kimberlite (Yakutia, Russia): Types, Compositions and Origins

Olivine is the principal mineral of kimberlite magmas, and isthe main contributor to the ultramafic composition of kimberliterocks. Olivine is partly or completely altered in common kimberlites,and thus unavailable for studies of the origin and evolutionof kimberlite magmas. The masking effects of alteration, commonin kimberlites worldwide, are overcome in this study of theexceptionally fresh diamondiferous kimberlites of the Udachnaya-Eastpipe from the Daldyn–Alakit province, Yakutia, northernSiberia. These serpentine-free kimberlites contain large amountsof olivine (50 vol.%) in a chloride–carbonate groundmass.Olivine is represented by two populations (olivine-I and groundmassolivine-II) differing in morphology, colour and grain size,and trapped mineral and melt inclusions. The large fragmentalolivine-I is compositionally variable in terms of major (Fo_85–94)and trace element concentrations, including H₂O content (10–136ppm). Multiple sources of olivine-I, such as convecting andlithospheric mantle, are suggested. The groundmass olivine-IIis recognized by smaller grain sizes and perfect crystallographicshapes that indicate crystallization during magma ascent andemplacement. However, a simple crystallization history for olivine-IIis complicated by complex zoning in terms of Fo values and traceelement contents. The cores of olivine-II are compositionallysimilar to olivine-I, which suggests a genetic link betweenthese two types of olivine. Olivine-I and olivine-II have oxygenisotope values (+ 5·6 ± 0·1 VSMOW, 1 SD)that are indistinguishable from one another, but higher thanvalues (+ 5·18 ± 0·28) in ‘typical’mantle olivine. These elevated values probably reflect equilibriumwith the Udachnaya carbonate melt at low temperatures and ¹⁸O-enrichedmantle source. The volumetrically significant rims of olivine-IIhave constant Fo values (89·0 ± 0·2 mol%),but variable trace element compositions. The uniform Fo compositionsof the rims imply an absence of fractionation of the melt'sFe²⁺/Mg, which is possible in the carbonatite melt–olivinesystem. The kimberlite melt is argued to have originated inthe mantle as a chloride–carbonate liquid, devoid of ‘ultramafic’or ‘basaltic’ aluminosilicate components, but becameolivine-laden and olivine-saturated by scavenging olivine crystalsfrom the pathway rocks and dissolving them en route to the surface.During emplacement the kimberlite magma changed progressivelytowards an original alkali-rich chloride–carbonate meltby extensively crystallizing groundmass olivine and gravitationalseparation of solids in the pipe. KEY WORDS: kimberlite; olivine; partial melting; carbonatitic melt; oxygen isotopes; H₂O     

The prediction of aquatic sediment-associated trace element concentrations using selected geochemical factors

Multiple linear regression models calculated from readily obtainable chemical and physical parameters can explain a high percentage (70 per cent or greater) of observed sediment-trace element variance for Cu, Zn, Pb, Cr, Ni, Co, As, Sb, Se, and Hg in a widely divergent suite of 61 sediment samples. The independent variables used in the models may be single parameters, principal component scores, or principal component scores combined with their cross-products. The most useful type of variable must be determined on a case-by-case basis. The independent variables (geochemical parameters) incorporated in the models calculated during this study probably are applicable to many aquatic sediments; albeit, use of a larger data set (>61) could alter the magnitude of the calculated coefficients. The geochemical parameters included in the models were of a physical (e.g. grain size, surface area) and a chemical (e.g. organic matter, amorphous iron oxides) nature. Comparison between actual and predicted trace element concentrations obtained from the models may provide a means of defining ‘average’ sediment-trace element concentrations. In this context, the models may also help identify either naturally or anthropogenically impacted sites for additional study.     

Computational Fluid Dynamical Modelling of Concentration Fluctuations in an Idealized Urban Area

Turbulent mixing induces variability in concentration that is important in many applications, such as reactive plumes, risk assessments or odour impact analyses (when the effects can have time scales on the order of a second). In urban canopies, the variability may be modified by the presence of buildings. Our purpose is to study concentration fluctuation variance in built-up areas using an Eulerian approach. We performed numerical simulations with the computational fluid dynamics model Mercure_Saturne, which is a three-dimensional model adapted to atmospheric flow and pollutant dispersion. We use a k − ϵ turbulence closure and predict the concentration variance with a transport equation model. The model performance is evaluated with the near-full scale experiment MUST (Mock Urban Setting Test), a field experiment conducted in Utah’s West Desert Test Center. The modelled root-mean-square of the concentration fluctuations is compared to measurements for 20 of the MUST trials. The model shows good agreement with the measurements, with the fraction of predictions within a factor of two of observations of 60.1%, with better results for horizontal lines of detectors than for the detectors on vertical masts (with fractions of predictions within a factor of two of observations of respectively 66.4% and 52.6%). The influence of different parameters on the fluctuation variance is also studied and we show the importance of taking into account the stability of the stratification when modelling the turbulent kinetic energy.     

Concentrations and annual fluxes of sediment‐associated chemical constituents from conterminous US coastal rivers using bed sediment data

Coastal rivers represent a significant pathway for the delivery of natural and anthropogenic sediment‐associated chemical constituents to the Atlantic, Pacific and Gulf of Mexico coasts of the conterminous USA. This study entails an accounting segment using published average annual suspended sediment fluxes with published sediment‐associated chemical constituent concentrations for (1) baseline, (2) land‐use distributions, (3) population density, and (4) worldwide means to estimate concentrations/annual fluxes for trace/major elements and total phosphorus, total organic and inorganic carbon, total nitrogen, and sulphur, for 131 coastal river basins. In addition, it entails a sampling and subsequent chemical analysis segment that provides a level of ‘ground truth’ for the calculated values, as well as generating baselines for sediment‐associated concentrations/fluxes against which future changes can be evaluated. Currently, between 260 and 270 Mt of suspended sediment are discharged annually from the conterminous USA; about 69% is discharged from Gulf rivers (n = 36), about 24% from Pacific rivers (n = 42), and about 7% from Atlantic rivers (n = 54). Elevated sediment‐associated chemical concentrations relative to baseline levels occur in the reverse order of sediment discharges: Atlantic rivers (49%) > Pacific rivers (40%) > Gulf rivers (23%). Elevated trace element concentrations (e.g. Cu, Hg, Pb, Zn) frequently occur in association with present/former industrial areas and/or urban centres, particularly along the northeast Atlantic coast. Elevated carbon and nutrient concentrations occur along both the Atlantic and Gulf coasts but are dominated by rivers in the urban northeast and by southeastern and Gulf coast (Florida) ‘blackwater’ streams. Elevated Ca, Mg, K, and Na distributions tend to reflect local petrology, whereas elevated Ti, S, Fe, and Al concentrations are ubiquitous, possibly because they have substantial natural as well as anthropogenic sources. Almost all the elevated sediment‐associated chemical concentrations found in conterminous US coastal rivers are lower than worldwide averages. Copyright © 2012 John Wiley & Sons, Ltd.     

A story of “communities”: boundaries,geographical composition and social coherence in a forest conservation project,Northern Cambodia

Explicit notions of “communities”, as key actors in conservation and development projects across the Global South, are common. Narratives about “indigenous people” or “forest-dependent communities” in forest conservation programmes prevail, portraying a picture of “communities” as homogeneous and harmonious entities. In this study, we unfold “communities” as a construct with an empirical example of a community-based forest protection project, Northern Cambodia. Based on qualitative interviews, field observations and document analysis, we examine the “community” construct in terms of establishment of boundaries, geographical composition and social coherence. We not only find that the establishment of forest “community” boundaries are dominated by powerful external actors rather than the “community members” themselves, but that the spatial composition of “communities” is complex, and affects the ability of local people to benefit from the project. We also find that the studied “communities” show low levels of social coherence and mainly consist of migrant farmers, as opposed to common policy narratives. Taking these inconsistencies into account, we discuss implications of constructing “communities” for the success of forest conservation projects, and argue in favour of more discursive and political analyses to better understand, acknowledge and adapt to existing and changing conditions in present and prospective project locations.