Thermoregulatory and osmoregulatory responses to dehydration in the bushy-tailed gerbil Sekeetamys calurus

Desert rodents are occasionally exposed to long spells of drought. We aimed to examine how such dehydrating conditions affect resting metabolic rate (RMR), non-shivering thermogenesis (NST) and osmoregulatory capabilities in the desert inhabiting species Sekeetamys calurus. Dehydration was imposed by gradually increasing salinity of drinking water and by feeding the animals a high-protein diet. S. calurus responded to osmotic stress by reducing RMR, increasing NST capacity, reducing urine volume and increasing urine concentration. It is suggested that the reduction in RMR is an adaptation for conserving water, while the increase in NST capacity compensates for the reduction in RMR.     

Compositions of aqueous fluids in equilibrium with pyroxenes and olivines at mantle pressures and temperatures

Solubility experiments were performed at 30 kbars in the system Mg₂SiO₄-SiO₂-H₂O, and at 20 and 30 kbars on omphacitic pyroxene-water mixtures. They confirm that the solubility of the forsterite component in aqueous fluids remains rather low (up to 5 wt.%), whereas the solubility of the SiO₂ component from solids of appropriate SiO₂-rich compositions in the system Mg₂SiO₄-SiO₂-H₂O increases with temperature up to some 75% at 1,100° C. At this temperature a simplified harzburgite consisting of forsterite and enstatite coexists with a fluid containing about 35% (MgO+SiO₂). Hydrous fluids coexisting with omphacitic clinopyroxenes leach sodium silicate component from the solid leaving less jadeitic pyroxenes behind. Most interestingly, the amount of sodium leached at constant temperature increases with decreasing pressure.Comparison of the results with previous solubility studies in the system K₂O-MgO-Al₂O₃-SiO₂-H₂O indicates that hydrous fluids in the mantle must be alkaline rather than silicanormative. Alkali metasomatism caused by such fluids would lead to potassium enrichment in deeper portions of the upper mantle and to sodium enrichment at shallower levels, where amphiboles become stable. This K/Na fractionation in the upper mantle may explain the generation of K-rich or of Na-rich magmas through partial melting at different depths.     

First terrestrial occurrence of roedderite in volcanic ejecta of the Eifel,Germany

Idiomorphic crystals of roedderite occur in melt-coated cavities of xenoliths of contact-altered quartz-sillimanite and quartz-feldspar gneisses which were ejected with the tephritic lava of the Bellerberg volcano. Physical and chemical properties of three different sets of crystals agree generally with those of roedderites from meteorites, in which so far the mineral had been found exclusively. In detail, however, there are characteristic chemical differences amongst the Eifel roedderites with one set of crystals matching closely the ideal formula (Na,K)₂Mg₅ Si₁₂O₃₀, a second set containing excess alkalies according to the substitution Na⁺0.5 Mg²⁺, and a third set richer in iron having an alkali deficiency following Fe³⁺Fe²⁺+Na⁺.The terrestrial roedderites are considered to be precipitates from highly alkaline, MgSi-rich, but Aldeficient gas phases that evolved through contact heating of the gneisses by the tephrite magma.     

Natural sodium phlogopite coexisting with potassium phlogopite and sodian aluminian talc in a metamorphic evaporite sequence from Derrag,Tell Atlas,Algeria

In its only natural occurrence known thus far sodium phlogopite is found in a dolomite containing large porphyroblasts of albite, three other magnesium phyllosilicates, dravite-uvite tourmaline, quartz, rutile, and pyrite. Sodium phlogopites are close to the ideal formula NaMg₃[AlSi₃O₁₀](OH)₂, although they may possibly contain additional Li. They are invariably coated by thin rims of potassium phlogopite with octahedral and tetrahedral occupancies different from those of sodium phlogopite. These rims may have prevented the retrograde hydration of sodium phlogopite which seems to be the main reason for its general absence in natural rocks. For the low-grade metamorphic conditions undergone by the dolomite a solvus relationship is indicated between sodium and potassium phlogopite.Sodium phlogopite also coexists, at least prior to the appearance of K phlogopite, with a talc phase containing Na and Al^[4] substituting for Si. This type of substitution leading from pure talc to sodium phlogopite was found to extend as far as 36 mole percent. However, the nature of this phase as a genuine solid solution or as a disordered mixed-layer between talc and sodium phlogopite could not be identified as yet. The final phyllosilicate appearing in millimeter-size porphyroblasts is an ordered 11 mixed layer between clinochlore and sodian aluminian talc representing a new mineral.Metamorphic temperatures at the supposedly low water and CO₂ fugacities are estimated to have been below 400 °C.     

Characteristics of storm waves off the Mediterranean coast of Israel

A two-year series of directional wave measurement off the Eastern Mediterranean coast of Israel reveals an abundance of high storm waves. Some of these waves have significant height in excess of 5 meters and periods as long as 15 sec.The evolution of the storm waves is described and related to the growth and paths of the storm fronts in Mid-Mediterranean. Shorter-period waves are found to always lead the arrival of longer-period swell. This characteristic is explained by a short decay distance and/or a high migration velocity of the storm front.The scatter plot of significant wave height vs period for the recorded events of each storm describes an open-loop time sequence. The difference in period between that of the peak height event and the period of a fully arisen sea of the same height is found to be indicative of the true decay distance the waves have travelled.     

Measurement of surface water runoff from plots of two different sizes

Intensities and amounts of water infiltration and runoff on sloping land are governed by the rainfall pattern and soil hydraulic conductivity, as well as by the microtopography and soil surface conditions. These components are closely interrelated and occur simultaneously, and their particular contribution may change during a rainfall event, or their effects may vary at different field scales. The scale effect on the process of infiltration/runoff was studied under natural field and rainfall conditions for two plot sizes: small plots of 0·25 m² and large plots of 50 m². The measurements were carried out in the central region of Chile in a piedmont most recently used as natural pastureland. Three blocks, each having one large plot and five small plots, were established. Cumulative rainfall and runoff quantities were sampled every 5 min. Significant variations in runoff responses to rainfall rates were found for the two plot sizes. On average, large plots yielded only 40% of runoff quantities produced on small plots per unit area. This difference between plot sizes was observed even during periods of continuous runoff. Copyright © 2002 John Wiley & Sons, Ltd.     

Century-scale nitrogen and phosphorus controls of the carbon cycle

In recent decades, humans have become a very important force in the Earth system, demonstrating that emissions (gaseous, liquid, and solid) are the cause of many of our environmental issues. These emissions are responsible for major global reorganizations of the biogeochemical cycles. The oceans are now a net sink of atmospheric CO₂, whereas in their preindustrial state they were a source; the trophic state of the coastal oceans is progressively moving toward increased heterotrophy; and the terrestrial realm is now vacillating between trophic states, whereas in preindustrial times it was autotrophic. In this paper, we present model calculations that underscore the role of human-induced perturbations in changing Earth's climate, specifically the role of anthropogenic nitrogen and phosphorus in controlling processes in the global carbon cycle since the year 1850 with projections to the year 2035. Our studies show that since the late 1940's emissions of nitrogen and phosphorus have been sequestered in the terrestrial living phytomass and groundwater. This nutrient-enhanced fertilization of terrestrial biota, coupled with rising atmospheric CO₂ and global temperature, has induced a sink of anthropogenic CO₂ that roughly balances the emission of CO₂ owing to land use change. In the year 2000, for example, the model-calculated terrestrial biotic sink was 1730 Mtons C/year, while the emission of CO₂ from changes in land use was 1820 Mtons C/year, a net flux of 90 Mtons C/year emitted to the atmosphere. In the global aquatic environment, enhanced terrestrial inputs of biotically reactive phosphorus (about 8.5 Mtons P/year) and inorganic nitrogen (about 54 Mtons N/year), have induced increased new production and burial of organic carbon in marine sediments, which is a small sink of anthropogenic CO₂. It is predicted that the response of the global land reservoirs of C, N, and P to sustained anthropogenic perturbations will be maintained in the same direction of change over the range of projected scenarios of global population increase and temperature change for the next 35 years. The magnitude of change is significantly larger when the global temperature increase is maximum, especially with respect to the processes of remobilization of the biotically important nutrients nitrogen and phosphorus.     

Effects of aqueous complexation on reductive precipitation of uranium by Shewanella putrefaciens

We have examined the effects of aqueous complexation on rates of dissimilatory reductive precipitation of uranium by Shewanella putrefaciens. Uranium(VI) was supplied as sole terminal electron acceptor to Shewanella putrefaciens (strain 200R) in defined laboratory media under strictly anaerobic conditions. Media were amended with different multidentate organic acids, and experiments were performed at different U(VI) and ligand concentrations. Organic acids used as complexing agents were oxalic, malonic, succinic, glutaric, adipic, pimelic, maleic, citric, and nitrilotriacetic acids, tiron, EDTA, and Aldrich humic acid. Reductive precipitation of U(VI), resulting in removal of insoluble amorphous UO₂ from solution, was measured as a function of time by determination of total dissolved U. Reductive precipitation was measured, rather than net U(VI) reduction to U(IV), to assess overall U removal rates from solution, which may be used to gauge the influence of chelation on microbial U mineralization. Initial linear rates of U reductive precipitation were found to correlate with stability constants of 1:1 aqueous U(VI):ligand and U(IV):ligand complexes. In the presence of strongly complexing ligands (e.g., NTA, Tiron, EDTA), UO₂ precipitation did not occur. Our results are consistent with ligand-retarded precipitation of UO₂, which is analogous to ligand-assisted solid phase dissolution but in reverse: ligand exchange with the U⁴⁺ aquo cation acts as a rate-limiting reaction moderating coordination of water molecules with U⁴⁺, which is a necessary step in UO₂ precipitation. Ligand exchange kinetics governing dissociation rates of ligands from U(VI)-organic complexes may also influence overall UO₂ production rates, although the magnitude of this effect is unclear relative to the effects of U(IV)-organic complexation. Our results indicate that natural microbial-aqueous systems containing abundant organic matter can inhibit the formation of biogenic amorphous UO₂.