Moho structure of Central America based on three-dimensional lithospheric density modelling of satellite-derived gravity data

The Central American isthmus hosts a highly variable Moho structure due to the diverse origin and composition of the crustal basement and the influence of large-scale neotectonic processes. Gravity data from the combined geopotential model EGM2008 were interpreted via forward modelling to outline the three-dimensional lithospheric density structure along the Middle American Trench, as well as the segmentation of the oceanic Cocos and Nazca plates and the overriding Caribbean plate. In this work, results for the depth of the Moho obtained from the density model are presented. The Quaternary volcanic arc correlates with a maximum Moho depth of 44 km in western Guatemala. To the south-east of the continental shelf, the Caribbean plate shows Moho depths between 20 and 12 km whereas to the north, values as shallow as 8 km are observed at the Cayman trough. For the oceanic Cocos plate, depths between 16 and 21 km are obtained for the Moho along the Cocos ridge, contrasting with values between 15 and 12 km for the seamount segment and 8 and 11 km for the segments of the crust that are not affected by the Galapagos hot-spot track.     

Phylogenetic Problems in Polynesian Simuliidae (Diptera: Culicomorpha): A progress report

As a basis for eventual control of the vicious anthropophilic and ornithophilic simuliid females of the Marquesas Islands, a taxonomic revision of Polynesian Simuliidae is in progress. Cytotaxonomic studies reveal two simuliid species in Rarotonga, Cook Islands; nine species in Tahiti, Society Islands, and two in the Marquesas Islands. A cytophylogeny is now available. Polynesian Simuliidae are unique in possessing heterogametic females. A reconstructed phylogeny, based mainly on morphological character states of larvae and pupae, agrees well with the cytophylogeny. One of the new species which is closely related to Simulium oviceps Edwards has larvae with highly reduced, non-functional cephalic fans. Ages of the Polynesian islands are discussed in relation to possible dispersal of Simuliidae into Polynesia.     

Modified biomass of Phanerochaete chrysosporium immobilized on luffa sponge for biosorption of hexavalent chromium

Phanerochaete chrysosporium, a white rot basidiomycete, was immobilized over Luffa cylindrica sponge discs, treated with 0.1 N HCl and its potentiality for the removal of hexavalent chromium [Cr(VI)] from water was investigated in both batch and in up-flow fixed-bed bioreactor. The acid treatment of biomass increased the uptake capacity and percentage removal of Cr(VI) from 33.5 to 46.5 mg g^?1 and 67 to 92 %, respectively. Maximum uptake of Cr(VI) was achieved at pH 2, temperature 40 °C after 100 min of contact time. The Cr(VI) sorption on the biomass was better explained by Langmuir isotherm. Thermodynamic studies indicated that the process was spontaneous and endothermic. Sorption kinetic study showed that pseudo-second-order model best correlates the Cr(VI) sorption on the biomass as compare to pseudo-first-order kinetic model. The performance of fixed-bed bioreactor was evaluated at different bed heights (5, 15 and 25 cm) and flow rates (1.66, 4.98 and 8.33 mL min^?1) by using bed depth service time model. Response surface methodology statistical method was applied for optimizing the process parameters. FTIR analysis showed that amino groups were mainly involved in adsorption of Cr(VI).     

Geochemical characteristics of tertiary oil-generating strata in Jiyang Sag

The Jiyang Sag was a near-sea basin in Oligocene time of mild and wet climate. The flourishing living things in this basin and the continuous depressions created a favorable environment for oil generation. Occasional transgressions resulted in special water-medium conditions, giving rise to a unique biological group of abundan terrestrial and fresh-water biota and organisms characteristic of semi-saline environments as well as small amounts of marine biota. Discussions are also made of the evolution of organic matter on the basis of changes of geochemical indexes for oil-generating rocks at different depths in the Dongying Depression.     

Breaking mode of cohesive homogeneous earth-rock-fill dam by overtopping flow

Breaking tests on homogeneous earth-rock-fill dams destroyed by overtopping flow are presented. Two types of shear erosion are found: wetting shear erosion and quick shear erosion; the water level-discharge process is divided into “sharp rise and drop of flow” and “slow change of flow” types. Furthermore, overtopping break modes are divided into head-cut erosion and scour breaching mode (Mode 1), shear erosion and collapse breaching mode (Mode 2), and wetting shear erosion mode (Mode 3) based on the main failure types and their coupled mode during dam break. In Mode 1, the downstream slope encounters head-cut erosion at the onset of the breach and expands and undercuts gradually at the development stage; in Mode 2, the dam slope encounters rapid shear erosion and the downstream edge of the crest erodes quickly towards the upstream face at the onset of breach: the breach expands suddenly due to instability and collapse at both sides of the breach in its development stage; in Mode 3, the strength of the dam’s materials continuously decreases by wetting and erosion happens is localised at positions where wetting caused the most strength loss, no obvious breach was developed. Dam breaking time, dam-break flow process, and the maximum discharge flow varied for each breaking mode. Overtopping flow size, materials, height, and initial breach size of dam are important factors influencing breaking mode, by virtue of their changing the relative strength of the relationship between the critical shear stress of dam materials at the edge of the dam crest and the lower parts of its slope, and the given flow’s destruction capacity. Overtopping will cause different manifestations of damage to be exhibited, so modal classification is favourable for safety assessment and preparation of relevant protective measures for protection of earth-rock-fill dam against overtopping.     

Temporal and spatial patterns in abundance and diversity of fish assemblages in Elkhorn Slough,California

Assemblages of ichthyofauna of shallow inshore habitats along Californía’s central coast are described in terms of species composition, abundance, and life-style categories. A total of 22,334 fishes from 65 species and 27 families was collected with otter trawls at six sites in the main channel and tidal creeks of Elkhorn Slough, a tidal embayment and seasonal estuary, and two nearshore ocean stations in Monterey Bay during 44 months between August 1974 and June 1980. Greater than 90% of the catch comprised 10 species. The four dominant species,Cymatogaster aggregata, Leptocottus armatus, Phanerodon furcatus, andEmbiotoca jacksoni, occurred during most or all seasons and were classified as residents or partial residents. Several abundant species were marine immigrants that seasonally use the slough as spawning and nursery grounds; this resulted in higher abundance and species richness during summer. Species collected during winter largely were slough residents. Species compsosition and richness varied with distance from the slough entrance. The ocean assemblage was most different, and its similarity to other stations decreased progressively with distance inland and into the tidal creeks. During our study, 5,074 fishes were collected by beach seine in Bennett Slough, a remote shallow marsh basin adjacent to the entrance of Elkhorn Slough. Species richness was relatively low and three euryhaline species accounted for >80% of the total catch. The species assemblage was most similar to those at the tidal creek and most shallow stations of Elkhorn Slough. Resident species numerically dominated assemblages in Bennett Slough and the most inland areas of Elkhorn Slough. The high relative abundance of marine-related fishes (classified as marine, marine immigrant, and partial resident), entering Elkhorn Slough early in life or as spawning adults indicates the importance of this habitat to nearshore fish assemblages.     

Simultaneous electrokinetic removal of polycyclic aromatic hydrocarbons and metals from a sediment using mixed enhancing agents

The maintenance of harbor waterways generates large amounts of dredged sediments which are often rich in coexisting organic and inorganic contaminants. Electrokinetic remediation treatments have recently been developed for the simultaneous removal of heavy metals and polycyclic aromatic hydrocarbons (PAHs), using various enhancing agents generally tested sequentially. In this study, different processing fluids were tested, alone or mixed, to improve the decontamination of aged model sediment contaminated with cadmium, lead, chromium, copper, zinc, and five PAHs. Nitric acid (NA) and citric acid (CA) were tested to avoid the formation of an alkaline front into the sediment and favor the metals removal, while an anionic surfactant [sodium dodecyl sulfate (SDS)] and a nonionic surfactant (Tween 20) were tested to solubilize and mobilize PAHs. Processing fluids were circulated under a constant voltage gradient of 1 V cm^?1 for 10–14 days. NA showed an excellent potential to remove metals (76.8–99.9 % removal) and PAHs (70.3–89.7 % removal) in a single run. Besides, the mixture of Tween 20 and CA, more environmental friendly, could be considered as a relatively good processing fluid for the simultaneous removal of metals (10.3–90.8 % removal) and PAHs (53.6–61.6 % removal) from the fine-grained sediment, while SDS mixed to CA was not a good candidate for this purpose (0.1–65 % removal for metals and 34.1–41.0 % removal for PAHs).     

Clicking graphene oxide and Fe3O4 nanoparticles together: an efficient adsorbent to remove dyes from aqueous solutions

Nanohybrid of graphene oxide (GO) and azide-modified Fe₃O₄ nanoparticles (NPs) were fabricated using click reaction. First, Fe₃O₄ NPs were modified by 3-azidopropionic acid. Then, click-coupling of azide-modified Fe₃O₄ NPs with alkyne-functionalized GO was carried out in the presence of CuSO₄·5H₂O and sodium l-ascorbate at room temperature. The attachment of Fe₃O₄ NPs onto the graphene nanosheets was confirmed by Fourier-transform infrared (FTIR) spectroscopy, scanning electron microscopy, thermogravimetric analysis, energy dispersive X-ray spectrometry and X-ray diffraction spectrometry. As the FTIR spectroscopy and energy dispersive X-ray spectrometry analysis showed, the final magnetic graphene nanosheets were also reduced by sodium ascorbate which is a merit for click-coupling reactions. The specific saturation magnetization of the Fe₃O₄-clicked GO was 44.3 emu g^?1. The synthesized hybrid was used in the adsorption of methylene blue and congo red (CR). The adsorption capacities in the studied concentration range were 109.5 and 98.8 mg g^?1 for methylene blue and CR, respectively.     

The application of a hierarchical Bayesian spatiotemporal model for forecasting the SAA trapped particle flux distribution

We implement a hierarchical Bayesian spatiotemporal (HBST) model to forecast the daily trapped particle flux distribution over the South Atlantic Anomaly (SAA) region. The National Oceanic and Atmospheric Administration (NOAA)-15 data from 1–30 March 2008 with particle energies as >30 keV (mep0e1) and >300 keV (mep0e3) for electrons and 80–240 keV (mep0p2) and > 6900 keV (mep0p6) for protons were used as the model input to forecast the flux values on 31 March 2008. Data were transformed into logarithmic values and gridded in a 5^°×5^° longitude and latitude size to fulfill the modelling precondition. A Monte Carlo Markov chain (MCMC) was then performed to solve the HBST Gaussian Process (GP) model by using the Gibbs sampling method. The result for this model was interpolated by a Kriging technique to achieve the whole distribution figure over the SAA region. Statistical results of the root mean square error (RMSE), mean absolute percentage error (MAPE), and bias (BIAS) showed a good indicator of the HBST method. The statistical validation also indicated the high variability of particle flux values in the SAA core area. The visual validation showed a powerful combination of HBST-GP model with Kriging interpolation technique. The Kriging also produced a good quality of the distribution map of particle flux over the SAA region as indicated by its small variance value. This suggests that the model can be applied in the development of a Low Earth Orbit (LEO)-Equatorial satellite for monitoring trapped particle radiation hazard.     

Crystal structures of Ni2SiO4 and Fe2SiO4 as a function of temperature and heating duration

X-ray structure refinements of Ni₂SiO₄ and Fe₂SiO₄ spinels have been made as a function of temperature and heating duration by intensity measurements at high temperatures and room pressure. The lattice parameters of Ni₂SiO₄ spinel linearly increased with temperature up to 1,000° C. However, Fe₂SiO₄ spinel exhibited a nonlinear thermal expansion and was converted to a polycrystalline mixture of spinel and olivine by heating of less than one-hour at 800° C. The ratios between the octahedral and tetrahedral bond lengths D _oct/D _tetr and between the shared and unshared edge distances (O-O)_sh/(O-O)_unsh in Fe₂SiO₄ spinel were both much larger than those in Ni₂SiO₄. These ratios increase with temperature. The Fe₂SiO₄ spinel more readily approached a activation state which facilitated the transition to the olivine structure than the Ni₂SiO₄ spinel. The lattice parameter of Ni₂SiO₄ spinel decreased with heating period at constant temperatures of 700° C and 800° C. The parameter of the quenched sample after heating for 52 h at 700° C was smaller than that of the nonheated sample. The refinements of the site occupancies at each heating duration indicated an increase in the cation deficiency in both tetrahedral and octahedral sites. Electron microprobe analysis, however, proved no significant difference in the chemical compositions between the quenched and nonheated samples. Si and Ni atoms displaced from normally occupied spinel lattice sites are assumed to settle in vacant sites defined by the cubic close packed oxygen sublattice in a manner which preserves the electric neutrality of the bulk crystal.     

A Sm-Nd isotopic study of the South Harris Igneous Complex,the Outer Hebrides

Sm-Nd geochronology may be used to bracket the age of metamorphism in rocks which are difficult to date by other methods. By coupling whole rock Sm-Nd analyses of the principal members of the South Harris Igneous Complex, with Sm-Nd mineral isochrons on two anothositic gabbros, the age of granulite facios metamorphism has been defined. Whole rock analyses of three pairs of closely spaced samples of the anorthosite give consistent ages averaging 2.18±0.06 Gyr, but in general the data from the anorthosite do not define an isochron as a result of variable contamination of the evolving magma chamber. Whole rock data on the tonalite indicate that it is younger than 2.06 Gyr; its mean T_CHUR age is 1.86±0.05 Gyr. Garnet-pyroxene-amphibole-plagioclase mineral isochrons on two anorthosite samples give identical 1.87±0.04 Gyr ages which date cooling after the high pressure granulite facies metamorphism. Together with the tonalite whole rock data this defines the age of that metamorphism and confirms Dearnley's original assignment of an early Laxfordian age.     

Levels and distributions of polycyclic aromatic hydrocarbons (PAHs) in middle reach of Huaihe River,China: anthropogenic influences and ecological risks

Polycyclic aromatic hydrocarbons (PAHs) are a group of aromatic hydrocarbons with high toxicity to human health. PAH emissions from industrial activities have become the primary sources of PAH contamination in Chinese watersheds. Here, we analyzed 10 individual priority PAHs in 120 water samples taken from middle reach of Huaihe River, China. The results show that the PAH levels in studied watershed are significantly lower as compared to other Chinese watersheds, approaching or slightly exceeding the PAH levels in watersheds from selected European and North American countries. We observe rather large variation in spatial and vertical PAH distributions, pointing to PAH inputs from local industrial emissions, and PAH cycle among atmosphere, water and sediment. Individual PAH ratios (i.e., phenanthrene/anthracene and fluorene/pyrene) and principal components analysis suggest a primarily pyrolytic PAH sources (combustion of coal and coke) in water column. Other accompanying PAH sources include emissions from steel industry and gasoline. Total toxic benzo[a]pyrene equivalent of PAHs in studied water column indicates that PAHs in watershed of middle reach of Huaihe River pose limited toxicity to the environment.     

Manganese deposits in northeastern European Russia and the Urals: Isotope geochemistry,genesis, and evolution of ore formation

Based on new data on the lithology, mineralogy, chemistry, and isotopic composition of manganese carbonate ores and rocks at the deposits and occurrences in the Novaya Zemlya Archipelago, the Pai-Khoi, and the Urals, as well as using data from the literature, the main Phanerozoic basins of manganese deposition have been established in the geological history of Laurasia, Pangea, and Siberian paleocontinents. The formation conditions of manganese ore gradually changed from hydrothermal-sedimentary in the Middle Paleozoic to sedimentary-diagenetic in Mesozoic and Cenozoic. The ore was also formed under catagenetic conditions. Carbon of oxidized organic matter plays a substantial role in the formation of manganese carbonates.     

Some examples of the Middle-Triassic Marine transgression in South-Western Mediterranean Europe

In Southwestern Mediterranean Europe (NE Spain, Sardinia and NW Apennines e. g. Monti Pisani and Punta Bianca) the Middle-Triassic transgression on a margin of an intracratonic basin appears to be controlled by the different morphology and tectonic activity of the margin itself. The analysis of some sequences leads to recognize three different kinds of margins:

1. margin with a narrow shelf sloping toward a very shallow restricted basin (Central and Southwestern Sardinia);
2. margin with a broad shelf gently sloping toward a shallow basin (NE Spain, Monti Pisani, NW Sardinia);
3. margin with a narrow shelf and steep slope marked by tectonic and volcanic activity (Punta Bianca).

     

Stability conditions of polycyclic aromatic hydrocarbons at high pressures and temperatures

The first results of study of stability of diverse polycyclic aromatic hydrocarbons at around 7 GPa and 773–1073 K are reported. Experiments were carried out in hydraulic multi-anvil presses. The run products after quenching were analyzed using a method of matrix-assisted laser desorption-ionization (MALDI). The formation of polymers of starting matters was determined at 7 GPa and 773–883 K. The polymers are characterized by atomic masses up to 5000 Da, that are multiple by masses of starting matters. At higher temperatures (873–1073 K), the selected PAHs and their polymers become unstable. The decomposition temperature of PAHs and their polymers exclude their stability under Earth’s mantle conditions. The studies could be of great significance for the low-temperature near-surface geodynamics of small and large planetary bodies, which supposedly contain hydrocarbon compounds.     

Sources and history of PAHs in lake sediments from oil-producing and industrial areas,northeast China

Abundance, sources, and historical records of polycyclic aromatic hydrocarbons (PAHs) in sediment cores of three lakes located in northeast China were evaluated. One lake was located in a rural oil field area, one in an industrial urban oil field area, and the third in an urban industrialized area without oil field influence. Cores from each lake were divided into 1-cm sections, dated using ¹³⁷Cs techniques, and 16 priority PAH compounds were measured. Total PAH concentrations were greater in industrial areas than in rural area, regardless of associated oil production. Only petroleum sources of PAHs were identified in lakes near oil fields between 1950s and 1980s, while sources of liquid fossil fuel combustion were persistently identified in the industrial urban lake. From 1990s to 2000s, PAH concentrations, especially high molecular weight PAHs, significantly increased in all lakes, which were consistent with the economic development in China, suggesting a change in energy use from wood burning and petroleum (oil) to liquid fossil fuel combustion. Environmental risk was low to moderate in sediments of the three lakes studied, and increases in high molecular weight PAHs during 1900s–2000s is a concern.     

Polycyclic aromatic hydrocarbons in surface sediments of Binacional Itaipu Lake,Brazil: characteristics,sources and toxicity evaluation

Itaipu Lake, which includes the Itaipu hydroelectric power plant, is one of the largest dams in the world and has a strong relationship with its surroundings. The flooded area has multiple uses such as navigation, recreation, water abstraction for industrial, urban and agricultural irrigation. The lake is located at the frontier between Brazil, Argentina and Paraguay. In this study, superficial sediments collected from nine sampling sites were analysed for grain size, organic matter and 16 priority polycyclic aromatic hydrocarbons (PAHs) using high-performance liquid chromatography (HPLC) with fluorescence detector. The total concentration of PAHs in the dry sediment ranged from 35.21 to 685.37 µg kg^?1. Diagnostic ratios showed that the possible source of PAHs in the Itaipu Lake could be pyrolitic and petrogenic. The potential toxicity of sediment of PAHs varied from not detected to 127.70 µg g^?1, suggesting that some adverse ecological effects would arise due to PAHs in these sediments.     

Electrical conductivity measurements on olivines and pyroxenes under defined thermodynamic activities as a function of temperature and pressure

Electrical conductivities of Ni₂SiO₄, Fe₂SiO₄, and MgSiO₃ were measured on synthetic powders in the temperature range 340° to 1,100° C and at pressures up to 20 kbars. For ternary compounds such as olivines and pyroxenes the control of two further variables, like the chemical activities of two components are needed, besides temperature and pressure. The activities of the corresponding binary oxides were controlled by equilibrating the samples with their neighbour-phases. Control of the oxygen partial pressure was achieved by buffer techniques. From the slopes of the lg σ vs. 1/T lines the activation energies were calculated for 10 kbar: 0.56 eV and 2.7 eV for Ni₂SiO₄ in equilibrium with SiO₂ and Ni/NiO-buffer for the temperature range 500°–800°C and 800°–1,000°C resp. 0.52 eV for Fe₂SiO₄ in equilibrium with SiO₂ and metallic iron, and 0.38 eV in equilibrium with SiO₂ and magnetite; 1.11 eV for MgSiO₃ in equilibrium with SiO₂, and 1.25 eV in equilibrium with Mg₂SiO₄.     

The structural role of Al2O3 and TiO2 in immiscible silicate liquids in the system SiO2-MgO-CaO-FeO-TiO2-Al2O3

The effects of the addition of Al₂O₃ on the large stable two liquid field in the SiO₂-TiO₂-CaO-MgO-FeO system were experimentally determined. The increase of Al₂O₃ content in the starting composition results in the decrease of critical temperature, phase separation and liquidus temperature of the two liquid field until it is rendered completely metastable. The shrinkage of the two liquid field indicates that Al₂O₃ is acting in the role of a network former and homogenizes the structure of the two melts. In this alkali-free system Al⁺³ utilizes the divalent cations, Ca⁺² and Mg⁺², for local charge balance with a preference for Ca⁺² over Mg⁺². Thus, AlO₄ tetrahedra combine with SiO₄ tetrahedra to form an aluminosilicate framework which polymerizes the SiO₂-poor melt and makes it structurally more similar to the SiO₂-rich melt. However, Ca⁺² and Mg⁺² are not as efficient in a charge balancing capacity as the monovalent K⁺ and Na⁺ cations. The lack of alkalis in this system limits the stability of AlO₄ tetrahedra in the highly polymerized SiO₂-rich melt and results in the preference of Al₂O₃ for the SiO₂-poor melt. The partitioning systematics of Ti are virtually identical to those of Al. It is concluded that Ti occurs in tetrahedral coordination as a network forming species in both the high — and low — SiO immiscible melts.     

Study of pocyclic aromatic hydrocarbons at a pressure of 6–9 GPa with X-ray diffraction and synchrotron radiation

This work is one of the stages of study of the deep C-O-H fluid and investigates the behavior of polycyclic aromatic hydrocarbons (PAHs) under conditions of the Earth’s mantle. The composition of the C-O-H fluid in the upper mantle is estimated as a mixture of H₂O and CH₄ with a minor amount of H₂ and heavier hydrocarbons. Some theoretical calculations show that the stability of heavy hydrocarbons (alkanes, alkenes, and PAHs) increases with an increase in temperature. This paper presents the results of an XRD study of PAHs stability in multianvil presses on a Spring-8 accelerator (Japan). The primary compositions were chosen according to the abundance of PAHs in nature. In situ diffraction spectrums were recorded to determine the PAHs stability field. It was established that the PAHs become unstable at a pressure of 6–9 GPa and a temperature of 873–1073 K.