Differential modulation of eastern oyster (<Emphasis Type="Italic">Crassostrea virginica</Emphasis>) disease parasites by the El-Niño-Southern Oscillation and the North Atlantic Oscillation

The eastern oyster (Crassostrea virginica) is affected by two protozoan parasites, Perkinsus marinus which causes Dermo disease and Haplosporidium nelsoni which causes MSX (Multinucleated Sphere Unknown) disease. Both diseases are largely controlled by water temperature and salinity and thus are potentially sensitive to climate variations resulting from the El Niño-Southern Oscillation (ENSO), which influences climate along the Gulf of Mexico coast, and the North Atlantic Oscillation (NAO), which influences climate along the Atlantic coast of the United States. In this study, a 10-year time series of temperature and salinity and P. marinus infection intensity for a site in Louisiana on the Gulf of Mexico coast and a 52-year time series of air temperature and freshwater inflow and oyster mortality from Delaware Bay on the Atlantic coast of the United States were analyzed to determine patterns in disease and disease-induced mortality in C. virginica populations that resulted from ENSO and NAO climate variations. Wavelet analysis was used to decompose the environmental, disease infection intensity and oyster mortality time series into a time–frequency space to determine the dominant modes of variability and the time variability of the modes. For the Louisiana site, salinity and Dermo disease infection intensity are correlated at a periodicity of 4 years, which corresponds to ENSO. The influence of ENSO on Dermo disease along the Gulf of Mexico is through its effect on salinity, with high salinity, which occurs during the La Niña phase of ENSO at this location, favoring parasite proliferation. For the Delaware Bay site, the primary correlation was between temperature and oyster mortality, with a periodicity of 8 years, which corresponds to the NAO. Warmer temperatures, which occur during the positive phase of the NAO, favor the parasites causing increased oyster mortality. Thus, disease prevalence and intensity in C. virginica populations along the Gulf of Mexico coast is primarily regulated by salinity, whereas temperature regulates the disease process along the United States east coast. These results show that the response of an organism to climate variability in a region is not indicative of the response that will occur over the entire range of a particular species. This has important implications for management of marine resources, especially those that are commercially harvested.     

Geophysical investigation using resistivity and GPR methods: a case study of a lubricant oil waste disposal area in the city of Ribeirão Preto,São Paulo,Brazil

Geophysics has been shown to be effective in identifying areas contaminated by waste disposal, contributing to the greater efficiency of soundings programs and the installation of monitoring wells. In the study area, four trenches were constructed with a total volume of about 25,000 m³. They were almost totally filled with re-refined lubricating oil waste for approximately 25 years. No protection liners were used in the bottoms and laterals of the disposal trenches. The purpose of this work is to evaluate the potential of the resistivity and ground penetrating radar (GPR) methods in characterizing the contamination of this lubricant oil waste disposal area in Ribeirão Preto, SP, situated on the geological domain of the basalt spills of the Serra Geral Formation and the sandstones of the Botucatu Formation. Geophysical results were shown in 2D profiles. The geophysical methods used enabled the identification of geophysical anomalies, which characterized the contamination produced by the trenches filled with lubricant oil waste. Conductive anomalies (smaller than 185 Ωm) immediately below the trenches suggest the action of bacteria in the hydrocarbons, as has been observed in several sites contaminated by hydrocarbons in previously reported cases in the literature. It was also possible to define the geometry of the trenches, as evidenced by the GPR method. Direct sampling (chemical analysis of the soil and the water in the monitoring well) confirmed the contamination. In the soil analysis, low concentrations of several polycyclic aromatic hydrocarbons (PAHs) were found, mainly naphthalene and phenanthrene. In the water samples, an analysis verified contamination of the groundwater by lead (Pb). The geophysical methods used in the investigation provided an excellent tool for environmental characterization in this study of a lubricant oil waste disposal area, and could be applied in the study of similar areas.     

Soil erosion prediction using the Revised Universal Soil Loss Equation (RUSLE) in a GIS framework,Chania, Northwestern Crete,Greece

Soil erosion is a growing problem in southern Greece and particularly in the island of Crete, the biggest Greek island with great agricultural activity. Soil erosion not only decreases agricultural productivity, but also reduces the water availability. In the current study, an effort to predict potential annual soil loss has been conducted. For the prediction, the Revised Universal Soil Loss Equation (RUSLE) has been adopted in a Geographical Information System framework. The RUSLE factors were calculated (in the form of raster layers) for the nine major watersheds which cover the northern part of the Chania Prefecture. The R-factor was calculated from monthly and annual precipitation data. The K-factor was estimated using soil maps available from the Soil Geographical Data Base of Europe at a scale of 1:1,000,000. The LS-factor was calculated from a 30-m digital elevation model. The C-factor was calculated using Remote Sensing techniques. The P-factor in absence of data was set to 1. The results show that an extended part of the area is undergoing severe erosion. The mean annual soil loss is predicted up to ∼200 (t/ha year⁻¹) for some watersheds showing extended erosion and demanding the attention of local administrators.     

Oxidation of the Kaapvaal lithospheric mantle driven by metasomatism

The oxidation state, reflected in the oxygen fugacity (fO₂), of the subcratonic lithospheric mantle is laterally and vertically heterogeneous. In the garnet stability field, the Kaapvaal lithospheric mantle becomes progressively more reducing with increasing depth from Δlog fO₂ FMQ-2 at 110 km to FMQ-4 at 210 km. Oxidation accompanying metasomatism has obscured this crystal-chemical controlled depth-fO₂ trend in the mantle beneath Kimberley, South Africa. Chondrite normalized REE patterns for garnets, preserve evidence of a range in metasomatic enrichment from mild metasomatism in harzburgites to extensive metasomatism by LREE-enriched fluids and melts with fairly unfractionated LREE/HREE ratios in phlogopite-bearing lherzolites. The metasomatized xenoliths record redox conditions extending up to Δlog fO₂ = FMQ, sufficiently oxidized that magnesite would be the stable host of carbon in the most metasomatized samples. The most oxidized lherzolites, those in or near the carbonate stability field, have the greatest modal abundance of phlogopite and clinopyroxene. Clinopyroxene is modally less abundant or absent in the most reduced peridotite samples. The infiltration of metasomatic fluids/melts into diamondiferous lithospheric mantle beneath the Kaapvaal craton converted reduced, anhydrous harzburgite into variably oxidized phlogopite-bearing lherzolite. Locally, portions of the lithospheric mantle were metasomatized and oxidized to an extent that conversion of diamond into carbonate should have occurred. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Combining TEM/resistivity joint inversion and magnetic data for groundwater exploration: application to the northeastern part of Greater Cairo,Egypt

This paper presents the combination of two complementary methods, magnetic and joint inversion of resistivity/TEM data, as an effective approach to characterize groundwater reservoirs. Twenty stations of transient electromagnetic (TEM) and vertical electrical soundings (VES) were measured and interpreted using a joint inversion technique to evaluate the subsurface low resistivity zones connected to the groundwater reservoir. A complementary survey including 871 land magnetic stations was carried out at the same area to detect the upper surface of the basaltic sheet, which represents the bottom of the Miocene aquifer in the study area. The geological log from one borehole drilled in the zone was used to partially calibrate the calculated models. The results revealed that the study area consists of five different geological units with ages ranging from Paleogene (Oligocene) to Quaternary. The methodology provides good results at a very low cost when compared with drilling boreholes.     

Hydrogeochemical stratification of the unconfined Samobor aquifer (Zagreb,Croatia)

In the western part of the city of Zagreb, Croatia, hydrogeochemical and isotopic investigations of the Samobor aquifer were carried out with the aim of determining the differences in hydrogeochemical characteristics at increasing aquifer depths. The aquifer comprises 40-m thick gravelly–sandy deposits, with lenses and interlayers of silt and clay. The analyses have proven that with increasing aquifer depth, there are decreases in groundwater temperature and the values of electrical conductivity and increases in the sodium, iron and manganese concentrations. The δ¹³C distribution shows an evident increase in biogenic carbon concentrations with increasing aquifer depth. The measured specific ¹⁴C activities showed that the deeper part of the aquifer is characterized by slow water exchange, while the shallower part is influenced by current recharge, although the pumping wells located on the well-field downstream penetrate the aquifer fully. A direct exchange of water from the Sava River and groundwater occurs in the near vicinity of the river. This exchange weakens further away, while the difference in hydrogeochemical characteristics between the Sava River water and groundwater increases.     

Gneiss-Water Interaction and Water Evolution During the Early Stages of Dissolution Experiments at Room Temperature

Gneiss-distilled water interaction at room temperature was investigated with batch-reactors to study water-rock reaction and geochemical evolution of the aqueous phase with time. The ion concentrations in water were controlled not only by the dissolution of primary minerals, but also by the precipitation of secondary minerals. The decreasing fraction sizes of gneiss could favor dissolution and precipitation simultaneously. Ca^2 and K^ were the major cations, and HCO3^- was the major anion in water. All the ions except Ca^2 increased in concentration with time. The Ca^2 release from the rock to the aqueous phase was initially much faster than the release of K^ , Na^2 and Mg^2 . But after about 5 - 24 hours, the Ca^2 concentrations in water decreased very slowly with time and became relatively stable. During the experiment, the water varied from the Ca-( K)-HCO3-type water to the K-Ca-HCO3-type water, and then to the K-(Ca, Na)-HCO3-type water. The water-gneiss interaction was dominated by the dissolution of Kfeldspar in the solution. The remaining secondary minerals were mainly kaolinite, illite and K (Mg) -mica.     

Stability at high-pressure,elastic behaviour and pressure-induced structural evolution of CsAlSi<Subscript>5</Subscript>O<Subscript>12</Subscript>, a potential host for nuclear waste

The elastic and structural behaviour of the synthetic zeolite CsAlSi₅O₁₂ (a = 16.753(4), b = 13.797(3) and c = 5.0235(17) Å, space group Ama2, Z = 2) were investigated up to 8.5 GPa by in situ single-crystal X-ray diffraction with a diamond anvil cell under hydrostatic conditions. No phase-transition occurs within the P-range investigated. Fitting the volume data with a third-order Birch–Murnaghan equation-of-state gives: V ₀ = 1,155(4) ų, K _T0 = 20(1) GPa and K′ = 6.5(7). The “axial moduli” were calculated with a third-order “linearized” BM-EoS, substituting the cube of the individual lattice parameter (a ³, b ³, c ³) for the volume. The refined axial-EoS parameters are: a ₀ = 16.701(44) Å, K _T0a = 14(2) GPa (β_a = 0.024(3) GPa^?1), K′ _a = 6.2(8) for the a-axis; b ₀ = 13.778(20) Å, K _T0b = 21(3) GPa (β_b = 0.016(2) GPa^?1), K′ _b = 10(2) for the b-axis; c ₀ = 5.018(7) Å, K _T0c = 33(3) GPa (β_c = 0.010(1) GPa^?1), K′ _c = 3.2(8) for the c-axis (K _T0a:K _T0b:K _T0c = 1:1.50:2.36). The HP-crystal structure evolution was studied on the basis of several structural refinements at different pressures: 0.0001 GPa (with crystal in DAC without any pressure medium), 1.58(3), 1.75(4), 1.94(6), 3.25(4), 4.69(5), 7.36(6), 8.45(5) and 0.0001 GPa (after decompression). The main deformation mechanisms at high-pressure are basically driven by tetrahedral tilting, the tetrahedra behaving as rigid-units. A change in the compressional mechanisms was observed at P ≤ 2 GPa. The P-induced structural rearrangement up to 8.5 GPa is completely reversible. The high thermo-elastic stability of CsAlSi₅O_12, the immobility of Cs at HT/HP-conditions, the preservation of crystallinity at least up to 8.5 GPa and 1,000°C in elastic regime and the extremely low leaching rate of Cs from CsAlSi₅O₁₂ allow to consider this open-framework silicate as functional material potentially usable for fixation and deposition of Cs radioisotopes.     

In situ estimation of the effective chemical diffusion coefficient of a rock matrix in a fractured aquifer

An in situ method of estimating the effective diffusion coefficient for a chemical constituent that diffuses into the primary porosity of a rock is developed by abruptly changing the concentration of the dissolved constituent in a borehole in contact with the rock matrix and monitoring the time-varying concentration. The experiment was conducted in a borehole completed in mudstone on the campus of the University of the Free State in Bloemfontein, South Africa. Numerous tracer tests were conducted at this site, which left a residual concentration of sodium chloride in boreholes that diffused into the rock matrix over a period of years. Fresh water was introduced into a borehole in contact with the mudstone, and the time-varying increase of chloride was observed by monitoring the electrical conductivity (EC) at various depths in the borehole. Estimates of the effective diffusion coefficient were obtained by interpreting measurements of EC over 34 d. The effective diffusion coefficient at a depth of 36 m was approximately 7.8×10^?6 m²/d, but was sensitive to the assumed matrix porosity. The formation factor and mass flux for the mudstone were also estimated from the experiment.