Modeling rhamnolipids production by Pseudomonas aeruginosa from immiscible carbon source in a batch system

A mathematical model to predict the rhamnolipids production by Pseudomonas aeruginosa from oleic acid in a two phase liquid-liquid batch reaction system, was developed in this study. The model was based on two theoretical assumptions: 1) the convective oleic acid mass transfer is coupled to a bioreaction in the aqueous liquid bulk, and 2) the volume of the immiscible oleic acid drops and the saturation concentration at the interface are a function of rhamnolipids production. The model was able to accurately predict the experimental growth of the Pseudomonas aeruginosa strain, and the rhamnolipids production data with oleic acid as carbon source. This mathematical approach indicated a high correspondence between the saturation dimensionless profiles of oleic acid at the interface and the experimental profiles of surface tension difference. This modeling approach may constitute a useful tool in the design and scaling-up of bioreactors applied to the production of biosurfactants with immiscible carbon sources.     

Über die Verteilung der aus Gezeitenbeobachtungen bestimmten gravimetrischen Faktoren in Europa

auamaumuu am, n u a¶rt;u nuu n ¶rt;a ₂, ₂, ₁ u ₁ (u. 1–4). na ¶rt;a ¶rt;am au ¶rt;um au an¶rt;u mu naam. a n¶rt;aam unam nu nuu nna m uu u u mmu mam ¶rt; uu u a a mau n.

---

---

Vorgetragen am 2. Internationalen Symposium Geodäsie und Physik der Erde, Potsdam, Mai 1973.     

Hydrostratigraphic framework and hydrogeological behaviour of the Mancha Oriental System (SE Spain)

The Mancha Oriental System (MOS) has a surface area of 7,260 km², making it one of the largest carbonate aquifer systems in Spain. The system sustains about 1,000 km² of irrigated crops and supplies groundwater to 275,000 inhabitants. The economic transformation brought about by the development of extensive irrigated cropland has led to a water-balance disequilibrium of about 75 million m³/year. This input–output deficit has negative consequences in the quantity and quality of the available resources, in the river–aquifer relationship, and in the associated ecosystems as well. To understand the hydrogeological behaviour of the system, it is necessary to design a conceptual model. Further, the conceptualisation of a groundwater flow system is a requirement of the European Water Framework Directive for the characterisation of groundwater bodies. The robustness of the conceptual model depends heavily on the user capability of representing the real system. In this work, a multidisciplinary approach has been used to represent the three-dimensional geological framework and the groundwater flow conceptualisation of the MOS. Data management and three-dimensional visualisation have been carried out by means of geographical information system (GIS) tools and software for contouring and three-dimensional surface mapping.     

P–T–t–d evolution of orogenic middle crust of the Roc de Frausa Massif (Eastern Pyrenees): a result of horizontal crustal flow and Carboniferous doming?

Structural, petrological and textural studies are combined with phase equilibria modelling of metapelites from different structural levels of the Roc de Frausa Massif in the Eastern Pyrenees. The pre‐Variscan lithological succession is divided into the Upper, Intermediate and Lower series by two orthogneiss sheets and intruded by Variscan igneous rocks. Structural analysis reveals two phases of Variscan deformation. D1 is marked by tight to isoclinal small‐scale folds and an associated flat‐lying foliation (S1) that affects the whole crustal section. D2 structures are characterized by tight upright folds facing to the NW with steep NE–SW axial planes. D2 heterogeneously reworks the D1 fabrics, leading to an almost complete transposition into a sub‐vertical foliation (S2) in the high‐grade metamorphic domain. All structures are affected by late open to tight, steeply inclined south‐verging NW–SE folds (F3) compatible with steep greenschist facies dextral shear zones of probable Alpine age. In the micaschists of the Upper series, andalusite and sillimanite grew during the formation of the S1 foliation indicating heating from 580 to 640 °C associated with an increase in pressure. Subsequent static growth of cordierite points to post‐D1 decompression. In the Intermediate series, a sillimanite–biotite–muscovite‐bearing assemblage that is parallel to the S1 fabric is statically overgrown by cordierite and K‐feldspar. This sequence points to ~1 kbar of post‐D1 decompression at 630–650 °C. The Intermediate series is intruded by a gabbro–diorite stock that has an aureole marked by widespread migmatization. In the aureole, the migmatitic S1 foliation is defined by the assemblage biotite–sillimanite–K‐feldspar–garnet. The microstructural relationships and garnet zoning are compatible with the D1 pressure peak at ~7.5 kbar and ~750 °C. Late‐ to post‐S2 cordierite growth implies that F2 folds and the associated S2 axial planar leucosomes developed during nearly isothermal decompression to <5 kbar. The Lower series migmatites form a composite S1–S2 fabric; the garnet‐bearing assemblage suggests peak P–T conditions of >5 kbar at suprasolidus conditions. Almost complete consumption of garnet and late cordierite growth points to post‐D2 equilibration at <4 kbar and <750 °C. The early metamorphic history associated with the S1 fabric is interpreted as a result of horizontal middle crustal flow associated with progressive heating and possible burial. The upright F2 folding and S2 foliation are associated with a pressure decrease coeval with the intrusion of mafic magma at mid‐crustal levels. The D2 tectono‐metamorphic evolution may be explained by a crustal‐scale doming associated with emplacement of mafic magmas into the core of the dome.     

Magnetic susceptibility and electrical conductivity as a proxy for evaluating soil contaminated with arsenic,cadmium and lead in a metallurgical area in the San Luis Potosi State,Mexico

A total of 113 samples of waste and soil were collected from a site in the state of San Luis Potosi, Mexico, that was occupied for several years by the metallurgical industry. Specific magnetic susceptibility (MS), electrical conductivity (EC) and pH were determined, as well as the total and available concentrations of potentially toxic elements (PTEs) such as As, Cd, Cu, Fe, Pb and Zn, which may cause a health risk for humans, animals and ecosystems, and the concentrations of major ions in aqueous extracts of soils and wastes. The solid phases of the samples were also characterized. The results revealed that the soils and wastes exhibited elevated values of PTEs, MS and EC. For soils these values decreased with increasing distance from the waste storage sites. The MS values were elevated primarily due to the presence of Fe-oxyhydroxides, such as magnetite, hematite and goethite, which contain PTEs in their structure leading to a high correlation between the value of MS and the As, Cd, Fe and Pb contents (r = 0.57–0.91) as well as between the PTEs values (r = 0.68–0.92). The elevated EC values measured in the metallurgical wastes were the result of presence of the sulfate minerals of Ca, Mg and Fe. The pollution index, which indicates the levels of simultaneous toxicity from elements such as As, Cd and Pb, was determined, with extreme hazard zones corresponding to areas that exhibit high MS values (0.91 correlation). In conclusion, MS measurements can be used as an indirect indicator to evaluate the PTE contamination in metallurgical areas, and EC measurements can aid in the identification of pollution sources.     

Late Carboniferous porphyry copper mineralization at La Voluntad,Neuquén,Argentina: Constraints from Re–Os molybdenite dating

The La Voluntad porphyry Cu–Mo deposit in Neuquén, Argentina, is one of several poorly known porphyry-type deposits of Paleozoic to Early Jurassic age in the central and southern Andes. Mineralization at La Voluntad is related to a tonalite porphyry from the Chachil Plutonic Complex that intruded metasedimentary units of the Piedra Santa Complex. Five new Re–Os molybdenite ages from four samples representing three different vein types (i.e., quartz–molybdenite, quartz–sericite–molybdenite and quartz–sericite–molybdenite ± chalcopyrite–pyrite) are identical within error and were formed between ~312 to ~316 Ma. Rhenium and Os concentrations range between 34 to 183 ppm and 112 to 599 ppb, respectively. The new Re–Os ages indicate that the main mineralization event at La Voluntad, associated to sericitic alteration, was emplaced during a time span of 1.7 ± 3.2 Ma and that the deposit is Carboniferous in age, not Permian as previously thought. La Voluntad is the oldest porphyry copper deposit so far recognized in the Andes and indicates the presence of an active magmatic arc, with associated porphyry style mineralization, at the proto-Pacific margin of Gondwana during the Early Pennsylvanian.     

Apophis: the Story Behind the Scenes

On December 20, 2004 the Minor Planet Center issued the Minor Planet Electronic Circular (MPEC) 2004-Y25 announcing the discovery of a new Near Earth Asteroid (NEA) with designation 2004 MN₄. Only two days later, when the Christmas holidays were about to begin, it was already apparent that this asteroid, currently known as Apophis, would be notorious: our close-approach monitoring system, CLOMON2, was already showing a Virtual Impactor (VI) in 2029 reaching the level 2 in the Torino Scale, the first asteroid to reach that level since our monitoring system had been operational. However, this was just the beginning of what it was to come in the subsequent days. In this paper we will give an overview of the NEODyS-CLOMON2 system and provide the details on how Apophis’ collision scenario evolved, the way NEODyS’ team handled it and the crazy 2004’ Christmas holidays we had due to this unexpected guest.     

A summary of sulfur dioxide emission rate measuremnts from Guatemalan volcanoes

Measurements of the sulfur dioxide (SO₂) emission rate from three Guatemalan volcanoes provide data which are consistent with theoretical and laboratory studies of eruptive and shallow magma chamber processes. In particular, unerupted magma makes a major contribution to the measured SO₂ emission rates at Santiaguito, a continuously erupting dacitic volcanic dome. Varying shallow magma convection rates can explain the variations in SO₂ emission rates at Santiaguito. At Fuego, a basaltic volcano currently in repose, SO₂ emission rate measurements are consistent with a high level magma body that is crystallizing and releasing volatiles. At Pacaya, a continuously erupting basaltic volcano, recent SO₂ emission rate measurements support laboratory simulation studies of strombolian eruptions; these studies indicate that the majority of gas escapes during eruptions and little gas escapes between eruptions.Average SO₂ emission rates over the last 20 years for Santiaguito, Fuego and Pacaya are 80, 160 and 260 Mg/d, respectively. On a global scale, these three volcanoes account for 1% of the annual global volcanic output of SO₂. Santiaguito and Pacaya, together, emit 6% of the total annual SO₂ emitted by continuously erupting volcanoes.Even though SO₂ measurements at these volcanoes have been made infrequently and by different investigators, the collective data help to establish a useful baseline by which to judge future changes. A more complete record of SO₂ emission rates from these volcanoes could lead to a better understanding of their eruption mechanisms and reduce the impact of their future eruptions on Guatemalan society.     

Study of Metal Distribution in Raw and Screened Swine Manure

The growth of industrial swine production over the last few years has led to a growth in concern over effluents generated by the activity. Several elements, mainly toxic metals, can be present in swine wastewater and can have a serious environmental impact. It is important, therefore, to know the metal concentration before the discharge of wastewater. In this work the temporal metal distribution in swine manure and its potential reduction using coarse (2 mm) and fine (<0.45 μm) liquid‐solid separation techniques were investigated. In order to do this, different swine manure sample preparation methods for Al, Ba, Cd, Co, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Sr and Zn determination by Inductively Coupled Plasma Optical Emission Spectrometry (ICP OES) were tested. The acid mixtures used to digest the manure sample significantly affected the metal recovery. Good analyte recoveries were observed with nitric acid/hydrogen peroxide mixtures or nitric acid/perchloric acid mixtures. Sulfuric acid/hydrogen peroxide mixtures produced inconsistent results and poor recoveries, mainly for Ba and Pb. It was observed that metal concentrations in swine manure varied greatly with time, up to one order of magnitude, due to changes in swine production such as feed and animal numbers. Metals concentrations observed in the raw wastewater exceeded Brazilian limits for discharge into water bodies and recommendations for agricultural use. Results obtained from the liquid‐solid separation study showed that metals in the raw swine manure were not removed with coarse screening. However, the major fraction of metals were removed by filtration (0.45 μm), with the exception of Na, K and Sr. Thus, the use of liquid‐solid separation techniques that capture the fine solid fractions (and associated metals) from raw manure can have a favorable impact on the environment and contribute to swine production wastewater treatment.