Enstatite-jadeite join and its role in the Earth's mantle

Phase relations on the enstatite-jadeite join were experimentally determined at solidus temperatures and 90–152 kb, and at 1400–2050°C/175–219 kb, with a split-sphere anvil apparatus (USSA-2000). New findings include immiscibility in garnet and determination of the stability of NaAlSiO₄ (calcium ferrite structure) with stishovite. A thermodynamic model for the enstatite-jadeite join was developed to calculate a complete phase diagram for the join at 500–2500°C and 0–270 kb. The results indicate that the two major discontinuities in the Earth's mantle at 400 and 670 km depths could correspond respectively to the formation and the breakdown of garnet with a pyroxene composition. A model for a chondritic upper mantle is proposed in which large-scale chemical and mineral layering was produced by fractionation of liquidus phases in a magma ocean. Solidification was completed at 400 km depth by crystallization of sodium-enriched residual melts, which produced a pyroxene layer at 300–400 km depths.     

Carbonatite melt inclusions in coexisting magnetite,apatite and monticellite in Kerimasi calciocarbonatite,Tanzania: melt evolution and petrogenesis

Kerimasi calciocarbonatite consists principally of calcite together with lesser apatite, magnetite, and monticellite. Calcite hosts fluid and S-bearing Na–K–Ca-carbonate inclusions. Carbonatite melt and fluid inclusions occur in apatite and magnetite, and silicate melt inclusions in magnetite. This study presents statistically significant compositional data for quenched S- and P-bearing, Ca-alkali-rich carbonatite melt inclusions in magnetite and apatite. Magnetite-hosted silicate melts are peralkaline with normative sodium-metasilicate. On the basis of our microthermometric results on apatite-hosted melt inclusions and forsterite–monticellite phase relationships, temperatures of the early stage of magma evolution are estimated to be 900–1,000°C. At this time three immiscible liquid phases coexisted: (1) a Ca-rich, P-, S- and alkali-bearing carbonatite melt, (2) a Mg- and Fe-rich, peralkaline silicate melt, and (3) a C–O–H–S-alkali fluid. During the development of coexisting carbonatite and silicate melts, the Si/Al and Mg/Fe ratio of the silicate melt decreased with contemporaneous increase in alkalis due to olivine fractionation, whereas the alkali content of the carbonatite melt increased with concomitant decrease in CaO resulting from calcite fractionation. Overall the peralkalinity of the bulk composition of the immiscible melts increased, resulting in a decrease in the size of the miscibility gap in the pseudoquaternary system studied. Inclusion data indicate the formation of a carbonatite magma that is extremely enriched in alkalis with a composition similar to that of Oldoinyo Lengai natrocarbonatite. In contrast to the bulk compositions of calciocarbonatite rocks, the melt inclusions investigated contain significant amount of alkalis (Na₂O + K₂O) that is at least 5–10 wt%. The compositions of carbonatite melt inclusions are considered as being better representatives of parental magma composition than those of any bulk rock.     

Reporting of cosmogenic nuclide data for exposure age and erosion rate determinations

We propose guidelines for the reporting of in situ cosmogenic nuclide data for exposure age and erosion rate determinations. This is motivated by the need to maintain the utility of such data in the future, and to delineate best scientific practice. These guidelines will allow published exposure ages and erosion rates to be recalculated with confidence by others in the future, if, as is likely, procedures to calculate cosmogenic nuclide production rates are modified in the meantime.     

On one method of solving the three-dimensional direct magnetic problem

Summary The solution of the direct magnetic problem is derived for three-dimensional bodies under the assumption that the components of the magnetization vector are analytical functions of the co-ordinates within the body being considered. The solution to the problem is given in the form of Green-type integrals and, much like with gravitational fields of inhomogeneous bodies, it may serve the purpose of solving the problem of the analytical continuation of the external field into the body.     

Two-pyroxene thermobarometry with new experimental data in the system CaO-MgO-Al2O3-SiO2

In the system CaO-MgO-Al₂O₃-SiO₂ (CMAS), equilibrium alumina contents of orthopyroxene and clinopyroxene, both coexisting with spinel + forsterite or spinel + anorthite, have been reversed in 16 runs at 1,300–1,400°C and 10.2–20.8 kbar, using PbO flux. The present data and the data of Perkins and Newton (1980) have been modeled using the Redlich-Kister equation. The resulting model satisfies most of the reversed data in the CMAS system, agrees very well with thermochemical measurements, and is consistent with the model for the enstatite-diopside join of Lindsley et al. (1981) and with the system MgO-Al₂O₃-SiO₂ of Gasparik and Newton (1984). The present data, however, do not confirm the negative slopes of Al-isopleths in the spinel lherzolite field suggested by Dixon and Presnall (1980). The new model has been used to calculate a graphical two-pyroxene thermobarometer applicable to natural two-pyroxene assemblages closely approaching in composition the CMAS system.     

Biogeochemistry of trace metals (Mn, Sr, Rb, Ba, Cu, Zn, Pb and Cd) in a river-wetland-lake system (Balaton Region, Hungary)

Mn, Sr, Ba, Rb, Cu, Zn, Pb and Cd concentrations have been measured seasonally in the water and deposited sediments of the system comprising: Zala river (main input) — Lakes Kis-Balaton 1 and 2 (small artificial lakes created in a former bay of Lake Balaton) — Keszthely bay (hypertrophic part of Lake Balaton). The concentrations of the trace elements together with pH, alkalinity, dissolved cations (Ca²⁺, Mg²⁺, Na⁺, and K⁺), dissolved inorganic ligands (Cl^–, SO₄ ^2–), particulate Al, Ca, inorganic and organic carbon are used to assess the contamination of the study area and biogeochemical processes controlling trace element concentrations. Thermodynamic speciation calculations have also been utilized to enhance our understanding of the system. In the sediments Rb, Ba, Cu and Zn concentrations were mainly controlled by the abundance of the aluminosilicate fraction. Strontium was mainly associated with the calcium carbonate fraction. The aluminosilicate fraction constitutes a major sink for Mn and Cd but the concentration of these elements are also strongly related to calcite precipitation. The main processes that control the dissolved distribution of trace elements in the Balaton system were: solid phase formation (carbonate) for Mn; coprecipitation with calcite for Sr, Ba, Rb and possibly Mn and Cd; adsorption/desorption processes (pH dependent) for Zn and Pb; solubilization of Mn and precipitation of Cd and Cu in reed covered wetland areas where anoxic conditions were probably existing during the warm season. A preliminary budget of atmospheric and river input to Lake Balaton has also been outlined. Although Lake Balaton, is subjected to anthropogenic inputs mainly from agricultural and domestic activities, their impact on trace element concentrations in the Balaton system is very limited due to the efficiency of removal processes (i.e. adsorption and co-precipitation) and to high sedimentation rates and strong sediment re-suspension. Anthropogenic inputs are only detected for Pb.     

Spatial organization of a shredder guild of caddisflies (Trichoptera) in a riffle - Searching for the effect of competition

The shredder guild plays an outstanding role in the functioning of headwater stream ecosystems by processing allochthonous leaf litter. Traditionally, the abiotic habitat template is regarded as the major determinant of its organization, and only a limited number of studies support the importance of biotic interactions. The aim of the present study was to examine whether competition plays a significant role in organizing the shredder guild of caddisflies in a riffle. Null-model based co-occurrence, co-existence and guild variation analyses were used in the study of guild organization. In addition, the traditional variance to mean ratio was applied for measuring the intraspecific aggregation of guild members. The non-significant metric values of co-occurrence and co-existence analyses predicted that competition was of limited importance in structuring the spatial organization of the shredder guild. The observed aggregated spatial distribution of species, suggests that besides stochastic events, deterministic forces should also contribute to the organization of the shredder guild of caddisflies.