Enhancements of CO and O3 from burnings in sugar cane fields

The manual harvest of sugar cane requires the burning of its foliage. This burning has strongly increased in Brazil after the National Alcohol Program was started which substituted automobile gasoline engines for alcohol engines. Presently, the source strength per unit area of this rural pollution is comparable to the well-known biomass burning source in Amazonia. The observed concentrations of CO and O₃ in the rural area of the state of São Paulo during the 1988 burning season were twice as large as those reported from an aircraft experiment of 1985 for biomass burnings of the tropical rain forest. Results are reported from airplane measurements and from three fixed ground stations. Mixing ratios of ozone and carbon monoxide in the height range below 6 km are normally less than 40 and 100 ppbv, (parts per billion by volume), respectively, in the absence of burnings. A strong O₃ and CO layer was observed during the burning period with peak concentrations of 80 ppbv of ozone and 580 ppbv of CO at about 2 km. The concentrations of CH₄ and CO₂ were also large, 1756 ppbv and 409 ppmv, respectively, at 1500 m. During the dry season period of the experiment, the ground based O₃ average diurnal variations obtained at the rural sites were practically identical to the typical urban variation observed at São José dos Campos, with daytime ozone values between 45 and 60 ppbv. A second three-day airplane excursion to the surgar cane fields in the wet season of 1989 has produces results to be contrasted with the dry (burning) season of 1988 and 1989. Carbon monoxide concentrations were below 100 ppbv at all heights and ozone concentrations were around 30–40 ppbv. The maximum daytime concentrations at the ground station Bauru was 25 ppbv of O₃, and at Jaboticabal it was 35 ppbv of O₃, only one half of what was observed in the dry season.Universidade Estadual de São Paulo.     

Intercrystalline cation partitioning between minerals of the triplite-zwieselite-magniotriplite and the triphylite-lithiophilite series in granitic pegmatites

Minerals of the triphylite-lithiophilite, Li(Fe, Mn)PO₄, and the triplite-zwieselite-magniotriplite series, (Mn, Fe, Mg)₂PO₄F, occur in the late stage period of pegmatite evolution. Unfortunately, neither are the genetic relationships between these phosphates fully understood nor are thermodynamic data known. Consequently, phosphate associations and assemblages from 8 granitic pegmatites — Clementine II, Rubicon II and III, and Tsaobismund (Namibia); Hagendorf-Süd and Rabenstein (Germany); Valmy (France); Viitaniemi (Finland) — have been tested for compositional zoning and intercrystalline partitioning of main elements by electron microprobe techniques. Although the selected pegmatites display varying degrees of fractionation, and the intergrowth textures indicate different genetic relationships between the phosphates, the plots of mole fractions X _Fe=Fe/(Fe+Mn+Mg+Ca), X _Mn=Mn/(Fe+Mn+Mg+Ca), and X _Mg=Mg/(Fe+Mn+Mg+Ca) can be fitted relatively well with smooth curves in Roozeboom diagrams. Their deviations from symmetrical distribution curves are mainly dependent upon X _Mg or X _Ca, and upon non-ideal solutions. Surprisingly small differences between the partition coefficients were detected for intergrowths of different origin. However, the partitioning of shared components among coexisting phases is clearly dependent upon the conditions of formation. Compositional zoning is observed only when both Fe–Mn phosphates are intergrown mutually or with other Fe–Mn–Mg mineral solid-solutios. Thus, the zoning does not seem to be due to continuous crystallization, but to later diffusion processes. The triplite structure has preference for Mn, Mg, and Ca, while Fe prefers minerals of the triphylite series. A quantification of main element fractionation between minerals of the triphylite and the triplite series is possible in the cases where diffusion can be excluded. For the Fe/(Fe+Mn) ratios of core compositions an equation with a high correlation coefficient (R=0.988) was determined: Fe/(Fe+Mn)_Tr=[Fe/(Fe+Mn)_Li]/{2.737-(1.737)[Fe/(Fe+Mn)_Li]} (Tr=triplite series, Li=triphylite series). Consequently, the Fe/(Fe+Mn) ratio of the triplite series can now also be used in the interpretation of pegmatite evolution, just like that of the triphylite series which has been successfully applied in the past.     

Evolution estivale de la turbidité dans le lac de Neuchâtel

Some turbiditic measures carried out by a limnological diffusiometer along with the physico-chemical determinations of the Lake of Neuchatel have permitted to subdivide the water column in 4 distinct layers: the Epilimnium, the Clear Water Layer, the Pelagic Nepheloid Layer and the Benthic Nepheloid Layer.      

Least-squares prediction of horizontal coordinate distortions in Canada

A least-squares prediction method is described to estimate horizontal coordinate distortions at lower order points of a network using known coordinate differences (NAD27 coordinate distortions Δϕ′s and Δλ′s) at higher order points between NAD27 coordinates and coordinates derived from a recent (MAY 76), relatively distortion free, adjustment of these points. Empirical autocovariance functions of Δϕ and Δλ and crosscovariance function between Δϕ and Δλ are derived from some 5,250 data points and modelled using series of exponential functions. Empirical mean square values of Δϕ and Δλ, which are a measure of the distortions in NAD27 ϕ and λ, are 0.051 and 0.645 arcsecs² respectively. The corresponding mean value of the product ΔϕΔλ, which is a measure of the correlation between Δϕ and Δλ, is 0.056 arcsecs². The accuracy obtainable for predicted Δϕ and Δλ at an arbitrary point (e.g., lower order station) is a function of the accuracy and configuration of known Δϕ′s and Δλ′s in the surrounding area. Accuracies obtainable for various types of data configuration are given. Under favorable conditions taking place in about 60% of cases, accuracies in terms of ms agreement with known values of 0″.02 (0.6 m) and 0″.01 (0.2 m along parallel at latitude 50°) for the predicted latitude and longitude distortions are obtainable. Finally, a comparison with a method based on the use of complex polynomials is made. Presented at International Symposium on Geodetic Networks and Computations, Munich, August–September 1981.     

Pressure and composition dependence of the electrical conductivity of iron-rich synthetic olivines to 200 kbar

The objectives of this study of olivines are, to calibrate the variation of electrical conductivity with pressure, up to 200 kbar in a diamond-anvil cell, and to determine how this is influenced by chemical composition. Experimentally, we have found that the variation of the electrical conductivity of three synthetic olivines containing 50, 75 and 100 mole percent of fayalite, is an exponential function of pressure P, closely represented at room temperature by:σ_xP=σ_x·exp ·(B _x·P) where x is the iron content of the olivine, σ _x the extrapolated value of conductivity at normal pressure and B _x the slope of the regression line in semi-logarithmic coordinates. It is thus possible to express the temperature dependence of conductivity through the Boltzmann relationship:σ_xPT= σ_αT· exp ·(-H*/RT)=σ_xT·exp ·[-(E*+PV _* ^x )/RT] where H* is the activation enthalpy, E* the activation energy and V _x ^* the activation volume. At constant temperature V _* ^x =B _x·RT and is approximately equal to 0,6 cm³/mole at 295 K. On the other hand, we have found that σ_xT is an exponential function of x and thus, B _x and of course V _x ^* are linear functions. The experimental procedure is described and the results discussed.     

The Relegation Algorithm

The relegation algorithm extends the method of normalization by Lie transformations. Given a Hamiltonian that is a power series = ₀+ ₁+ ... of a small parameter , normalization constructs a map which converts the principal part ₀into an integral of the transformed system — relegation does the same for an arbitrary function [G]. If the Lie derivative induced by [G] is semi-simple, a double recursion produces the generator of the relegating transformation. The relegation algorithm is illustrated with an elementary example borrowed from galactic dynamics; the exercise serves as a standard against which to test software implementations. Relegation is also applied to the more substantial example of a Keplerian system perturbed by radiation pressure emanating from a rotating source.This revised version was published online in October 2005 with corrections to the Cover Date.     

Astronomical time scale for the Middle Oxfordian to Late Kimmeridgian in the Swiss and French Jura Mountains

Detailed investigation of facies and sedimentary structures reveals that, during the Middle Oxfordian to Late Kimmeridgian, the shallow carbonate platform of the Swiss and French Jura Mountains recorded high-frequency sea-level fluctuations quite faithfully. The cyclostratigraphic analysis within the established biostratigraphic and sequence-chronostratigraphic framework implies that the resulting hierarchically stacked depositional sequences formed in tune with the orbital cycles of precession (20 kyr) and eccentricity (100 and 400 kyr). The astronomical time scale presented here is based on the correlation of 19 platform sections and 4 hemipelagic sections from south-eastern France where good biostratigraphic control is available. The cyclostratigraphic interpretation suggests that the interval between sequence boundaries Ox4 and Kim1 (early Middle Oxfordian to earliest Kimmeridgian) lasted 3.2 myr and that the Kimmeridgian sensu gallico has a duration of 3.2 to 3.3 myr. The astronomical time scale proposed here is compared to time scales established by other authors in other regions and the discrepancies are discussed. Despite these discrepancies, there is a potential to estimate the durations of ammonite zones and depositional sequences more precisely and to better evaluate the rates of sedimentary, ecological and diagenetic processes. Editorial handling: Hanspeter Funk, Helmut Weissert, Stefan Bucher     

Study of the erosion rates in the upper Maracujá Basin (Quadrilátero Ferrífero/MG,Brazil) by the in situ produced cosmogenic 10Be method

The present work quantifies the erosive processes in the two main substrates (schists–phyllites and granites–gneisses) of the upper Maracujá Basin in the Quadrilátero Ferrífero/MG, Brazil, a region of semi‐humid tropical climate. Two measuring methods of concentration were used: (i) in situ produced ¹⁰Be in quartz veins (surface erosion rates) and (ii) ¹⁰Be in fluvial sediments (basin erosion rates). The results confirm that (i) erosion tends to be more aggressive close to the headwaters than in the lower parts of the basin and (ii) the region is now affected by dissection. Copyright © 2006 John Wiley & Sons, Ltd.