Evolution of fluid geochemistry at the Turrialba volcano (Costa Rica) from 1998 to 2008

Turrialba (10°02′N, 83°45′W) is a 3,349-m high stratovolcano belonging to the Holocene “Cordillera Central” volcanic belt of Costa Rica. The summit consists of three EW-oriented craters (East, Central, and West). Since its last eruptive phase (1864–1866), the Central and West craters have displayed modest fumarolic activity, with outlet temperatures clustering around 90°C. In 2001, seismic swarms, ground deformation, and increasing fumarolic activity occurred. From 2005 to 2008, new fumarolic vents opened between and within the Central and West craters, and along the western and southwestern outer flanks of the volcanic edifice. These physical changes were accompanied by a drastic modification in the gas chemistry that can be divided in three stages: (1) hydrothermal (from 1998 to autumn 2001), characterized by the presence of H₂O, CO₂, H₂S, and, to a very minor extent, HCl and HF; (2) hydrothermal/magmatic (autumn 2001–2007), with the appearance of SO₂ and a significant increase of HCl and HF; and (3) magmatic-dominated (2007–2008), characterized by increased SO₂ content, SO₂/H₂S > 100, and temperatures up to 282°C. Accordingly, gas equilibrium in the CO₂-CH₄-H₂ system suggests a progressive evolution of the deep fluid reservoir toward higher temperatures and more oxidizing conditions. The chemical–physical modifications of Turrialba in the last decade can be interpreted as part of a cyclic mechanism controlling the balance between the hydrothermal and the magmatic systems. Nevertheless, the risk of rejuvenation of the volcanic activity cannot be excluded, and an appropriate seismic, ground deformation, and geochemical monitoring program is highly recommended. Turrialba lies at a distance of 35 and 15 km from San José and Cartago, respectively, the two largest cities in Costa Rica.     

Controlling factors and environmental implications of mercury contamination in urban and agricultural soils under a long-term influence of a chlor-alkali plant in the North–West Portugal

This study aims at assessing the extent of total mercury (Hg) contamination in urban and agricultural soils under long-term influence of a chlor-alkali plant, located at about 1 km away from a town centre. Moreover, it aims at identifying the main factors controlling Hg contents’ distribution and associated potential hazards to environment and human health. The median value of total Hg for soil surface layer (0–10 cm) was 0.20 mg/kg (data ranging from 0.050 to 4.5 mg/kg) and for subsurface layer (10–20 cm) 0.18 mg/kg (data ranging from 0.046 to 3.0 mg/kg). The agricultural area showed higher Hg concentrations (ranging from 0.86 to 4.5 mg/kg) than urban area (ranging from 0.05 to 0.61 mg/kg), with some results exceeding target values set by the Dutch guidelines. Mercury concentrations observed in the studied area are more likely to be associated with the influence of the chlor-alkali plant and with the use of historically contaminated sludges and water from a nearby lagoon in agriculture, than to the impacts of urban development. The statistical correlations between Hg concentrations and soil properties suggest that anthropogenic metal sources should influence the spatial distribution more than the geological properties. Although the Hg emissions were drastically reduced 10 years ago, the area under influence of the chlor-alkali plant is still facing potential health and environmental threats arising from soil contamination.     

Bacterial Community Dynamics in a Seagrass (<Emphasis Type="Italic">Posidonia oceanica</Emphasis>) Meadow Sediment

Some traits of the bacterial community dynamics associated to the rhizosphere of the Mediterranean seagrass Posidonia oceanica, growing in carbonate sediments, were analyzed during a 2-year period in an enclosed bay of the Balearic Islands. The diversity of the bacterial community was studied by the construction of 16S rDNA clone library. For testing temporal and vertical differences in the abundance of total cells and active Bacteria, we used 4′,6-diamidino-2-phenylindole (DAPI) staining and fluorescence in situ hybridization (FISH). Moreover, some relevant groups of sulfate-reducing bacteria (SRB) were occasionally assessed by FISH. Despite the observed decrease in the total DAPI-stained cells, bacterial counts, and sulfate reduction rates throughout the sampling time, we found an increase in both the pore-water sulfide concentration and the proportion of SRB. Overall, the results revealed a very high bacterial diversity and indicated shifts in bacterial dynamics that could not be related to temperature-dependent factors, suggesting a link between the documented regression of the seagrass meadow and the decline of the microbial community, likely due to large organic matter inputs to the bay.     

Inputs of organic carbon from Ria de Aveiro coastal lagoon to the Atlantic Ocean

Land/ocean boundaries constitute complex systems with active physical and biogeochemical processes that affect the global carbon cycle. An example of such a system is the mesotidal lagoon named Ria de Aveiro (Portugal, 40°38′N, 08°45′W), which is connected to the Atlantic Ocean by a single channel, 350 m wide. The objective of this study was to estimate the seasonal and inter-tidal variability of organic carbon fluxes between the coastal lagoon and the Ocean, and to assess the contribution of the organic carbon fractions (i.e. dissolved organic carbon (DOC) and particulate organic carbon (POC)) to the export of organic carbon to the Ria de Aveiro plume zone. The organic carbon fractions fluxes were estimated as the product of the appropriate fractional organic carbon concentrations and the water fluxes calculated by a two-dimensional vertically integrated hydrodynamic model (2DH). Results showed that the higher exchanges of DOC and POC fractions at the system cross-section occurred during spring tides but only resulted in a net export of organic carbon in winter, totalling 85 t per tidal cycle. Derived from the winter and summer campaigns, the annual carbon mass balance estimated corresponded to a net export of organic carbon (7957 = 6585 t yr⁻¹ POC + 1372 t yr⁻¹ DOC). On the basis of the spring tidal drainage area, it corresponds to an annual flux of 79 g m⁻² of POC and 17 g m⁻² of DOC out of the estuary.     

Granulometric selectivity in Liza ramado and potential contamination resulting from heavy metal load in feeding areas

The stomach contents of thin-lipped grey mullets Liza ramado were analysed in terms of granulometric composition and compared to the sediment of potential feeding areas in the Tagus estuary. Total organic matter (TOM) content and heavy metal content were determined in the surface sediment of three areas and eight trace elements were quantified: Cd, Co, Cr, Cu, Hg, Ni, Pb and Zn. The three sampled areas did not differ in TOM; and the heavy metal content was below Effects Range-Low level for most elements. The mean observed concentrations were present in the following sequence: Zn > Pb > Cr > Cu ≈ Ni > Co > Cd > Hg. Stomach contents granulometric composition provided information about the feeding selectivity of the mullets. Sediment fractions with particle size between 20 and 50 μm are preferred, independently of the fishes' length. Smaller standard length (SL) fishes have a higher positive selection of fine grained sediments than those with a larger SL. Finer fractions usually have higher concentration of heavy metals, which makes younger specimens of the thin-lipped grey mullet potentially more exposed to heavy metal load in the estuary. Metal concentration was not independent from the sampling point, presenting higher values near the margins and the estuary tidal drainage system. This means that during the first period of each tidal cycle, the mullets will feed first on the most contaminated areas, as a consequence of their movement following the rising tide to feed on previously exposed areas.     

Carbonaceous materials in size-segregated atmospheric aerosols from urban and coastal-rural areas at the Western European Coast

A high-volume cascade impactor, equipped with a PM10 inlet, was used to collect size-segregated aerosol samples during the summer of 2004 at two Portuguese locations: a coastal-rural area (Moitinhos) and an urban area (Oporto). Concentrations of airborne particulate matter (PM), total carbon (TC), organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) were determined for the following particle size ranges: < 0.49, 0.49–0.95, 0.95–3.0, and 3.0–10 µm. The total PM mass concentrations at the urban and coastal-rural sites ranged from 22.8 to 79.6 μg m^− 3 and 19.9 to 28.2 μg m^− 3, respectively, and more than 56% of the total aerosol mass was found in the fractions below 3.0 μm. At both locations the highest concentrations of OC and EC were found in the submicrometer size range. The regional variability for the OC and EC concentrations, with the highest concentrations being found in the urban area, was related to the contribution of local primary sources (mostly traffic emissions). It was also verified an enrichment of the small size particles in WSOC, representing on average 37.3(± 12.4)% and 59.7(± 18.0)% of OC in the very fine aerosol at the coastal-rural and urban areas, respectively. The amount of secondary OC calculated by the minimum OC/EC ratio method indicates that secondary organic aerosol formation was important throughout the study at both sites. The obtained results suggest that long-range transport and favourable summer conditions for photochemical oxidation are key factors determining secondary OC formation in the coastal-rural and urban areas. The ultraviolet absorption properties of the chromophoric constituents of the WSOC fractions were also different among the different particle size ranges and also between the two sampling locations, thus suggesting the strong impact of the diverse emission sources into the composition of the size-segregated organic aerosol.     

An effective Lagrangian description of supernova-core bounce

In standard hydrodynamical supernova computations many variables are needed to describe the time evolution of the stellar core. A numerical grid of points is usually constructed to attain the desirable accuracy. This fact limits the codes to run in the biggest and fastest computers. A new semi-analytical approach for the problem of the dynamical evolution of the collapse, bounce and explosion of a supernova core is proposed. The relevant coordinates of the dynamical problem are chosen to define an effective Lagrangian. The Lagrangian variables are the radii of the shells, seen now as collective coordinates, which describe the global aspects of the process. An effective Lagrangian with these properties for any number of shells is presented. The equations of motion are obtained from this Lagrangian and then integrated numerically. The potentiality of the method is exemplified for the extreme case in which only two shells are used to describe the stellar core. Even in this instance, it is possible to discuss the circumstances for the occurrence of supernova explosion.     

The Juiz De Fora Granulite Complex of the Central Ribeira Belt, SE Brazil: A Paleoproterozoic Crustal Segment Thrust During the Pan-African Orogeny

The granulites of the Juiz de Fora complex occur within thick basement thrust slices associated with the Pan-African shortening process in the central segment of the Ribeira belt. Five lithological units of the Intermediate tectonic domain of the belt can be identified on the basis of detailed geological mapping: a) orthogranulites, b) orthogneisses; c) kinzigite; d) intrusive garnet charnockite and e) amphibolite facies metasediments of probable Meso to Neoproterozoic age, correlated to the cover of the belt. Petrological data indicate high temperatures and intermediate to low lithostatic pressure conditions for the Paleoproterozoic granulite facies metamorphism. Textures and CO₂-rich fluid inclusions are probably related to an IBC path. Geochemical data do not show relevant compositional change as a result of the granulite metamorphism. Two calc-alkaline suites and tholeiitic to alkaline basic rocks can be related to compressional and extensional settings, respectively. The overall composition of the granulites, the lack of substantial LILE depletion as well as the composition of the fluid inclusion points to granulitization process driven by CO₂-rich fluids. Orthogranulites gave rise to banded gneisses as a result of the Pan-African retrograde metamorphism and intense deformation. The U and Th depletion detected in few rocks is possibly related with the hydrated conditions of the retrograde reactions.