Sodian stellerite from Capo Pula,Sardegna

The sodian stellerite (a zeolite) occurs as lustrous white or slightly pink, easily cleavable lamellae, filling cavities and fractures in an acid lava (andesite or rhyolite) in the cliff below S. Efisio Tower, near Capo Pula, Cagliari, Sardegna, Italy. The principal forms present are {010}, {011}, {111}. Single crystal photographs show an orthorhombic symmetry and Ammm (or Ammm) space group. An indexed X-ray diffraction powder pattern is provided. Unit cell dimensions, chemical formula, density, optical properties and thermal behaviour are given.     

Prediction of influence of global warming on biological cycle and carbon balance in forest ecosystems of the Volga River Basin

The gradient (ordination) analysis was used to find the tendencies and the rate of changes in discrete parameters of the cycle of forest phytomasses accompanying a growing thermoarid climatic trend. The prognostic estimates of biotic regulation of the carbon cycle by forest biogeocenoses according to the HadCM3 (version A2) climatic scenarios, describing the most powerful coming global warming, are presented.     

Enhancement of the method of summer precipitation forecasting

The physical-synoptic principles of the automated method of summer precipitation forecasting introduced into operational prognostic practice in 2006 by the decree of the Central Methodical Commission of the Federal Service for Hydrometeorology and Environmental Monitoring (Roshydromet) are presented. Beside that, improved modifications of this method, which are automatically updated, are shown. Validation of those updates based on observational data collected in 2004 has shown improvement of all major criteria of forecasts efficiency. The performed improvement is based on the more detailed quantitative realization of mechanism of various showers formation (including heavy rainfalls).     

Réflexions sur la contingence des lois de la Nature

There are two fundamental conceptions concerning the laws of nature — these laws are eternal or they may vary in the course of time. We suggest an experiment in order to find an intermediary thesis — i.e. to discover that law, if it really exists, according to which a given law of nature varies, or, at least, to find out the direction in which this variation is performed.     

Fire and vegetation shifts in the Americas at the vanguard of Paleoindian migration

Across North and South America, the final millennia of the Pleistocene saw dramatic changes in climate, vegetation, fauna, fire regime, and other local and regional paleo-environmental characteristics. Rapid climate shifts following the Last Glacial Maximum (LGM) exerted a first-order influence, but abrupt post-glacial shifts in vegetation composition, vegetation structure, and fire regime also coincided with human arrival and transformative faunal extinctions in the Americas. We propose a model of post-glacial vegetation change in response to climatic drivers, punctuated by local fire regime shifts in response to megaherbivore-driven fuel changes and anthropogenic ignitions. The abrupt appearance of humans, disappearance of megaherbivores, and resulting changes in New World fire systems were transformative events that should not be dismissed in favor of climate-only interpretations of post-glacial paleo-environmental shifts in the Americas. Fire is a mechanism by which small human populations can have broad impacts, and growing evidence suggests that early anthropogenic influences on regional, even global, paleo-environments should be tested alongside other potential causal mechanisms.     

The use of acidimetric titration as a novel approach to study particulate trace metal speciation and mobility: Application to sediments of the Scheldt estuary

The study of trace metal speciation has benefited from a great deal of interest leading to the development and the diversification of sequential extraction schemes (SES), which triggered the need for harmonization by the standard, measurements and testing programme (SM & T). However, some uncertainties still persist in the application of the harmonized 3-step protocol, because of the difficulty in conceptualizing a technique that can be applied to environmental samples irrespective of their nature. The alternative method proposed in this study is based on the solubility of the sample components progressively dissolved during the course of an acidimetric titration by 1 mol L⁻¹ HCl. The major HCl-reactive mineralogical components are identified using mass balance calculation of H⁺ consumed by their dissolution together with the amount of major elements released into solution. The speciation of minor and trace elements is investigated by comparing their titrations to those of the major elements. This approach is much simpler than SES because it uses simple non-selective H⁺ at room temperature instead of a complex experimental design of so-called specific reagents. The different mineral components of the solid are no longer operationally defined and the problem of selectivity is irrelevant to the titration approach. The method was applied to several sediment samples from the Scheldt estuary and the particulate phase was further examined by Scanning Electron Microprobe and X-ray Diffraction techniques. The nearly complete consumption of H⁺ in the suspension is balanced by the total dissolution of carbonates and Fe-oxyhydroxides. In contrast to the speciation inferred from the Tessier SES, the acidimetric titration has demonstrated that the carbonate phase does not significantly contain trace metals with the exceptions of 40% of the Mn and 30% of the Co. In contrast, the Fe-oxyhydroxides seem to play a major role and account for 70% of Pb and 20% of Cr, in addition to 60% of P and additional amounts of 20% Co and 40% Mn. 70% of the Cu also occur in the oxyhydroxide phase, more likely coprecipitated with gibbsite. 90% of the Cd and 85% of Zn can be attributed to the Acid Volatile Sulfide (AVS) phase as evidenced from S titration. The acidimetric titration method not only provides information on the speciation of trace metals but also allows the quantification of their reactivity and mobility, if one considers that the titration roughly mimics pH changes that may occur as a result of chemical disequilibrium in the environment. The results demonstrate the potential of the acidimetric titration as an alternative to SES protocols in geochemical and environmental regulation studies. This method is applicable to a wide variety of environmental materials with little or minor adjustments.     

Biosorption of Rare-Earth Elements and Yttrium by Heterotrophic Bacteria in an Aqueous Environment

This paper reports the results of the experimental determination of the coefficient of sorption of rare-earth elements and yttrium (REY) under conditions of acidic pH using several strains of heterotrophic bacteria (Microbacterium sp., Curtobacterium sp., Bacillus subtilis, Pseudomonas putida, and Bacillus pumilis) that are widespread in natural and technogenic waters of the Far East (Russia). Insignificant fractionation between heavy and light rare-earth elements, negative cerium and dysprosium anomalies, and a positive europium anomaly were revealed. The selectivity of REY biosorption by gram-positive and gram-negative bacteria, as well as inertia of the biosorption process under more acidic conditions of the medium, were shown.