Biodegradation of palmarosa oil (green oil) by Serratia marcescens

Biodegradation of oil depends on the nature of the oil, the type of microbial community and a variety of environmental factors. Green oils are being used as consumer goods and as raw materials in industries such as food processing, pharmaceutical and cosmetic. Microbial contaminations of green oils have been the cause of degradation problems. Serratia Marcessens produced cytochrome oxidase, catalase, Dextrose, Lactose, Manose and sorbitol enzymes were the main reason for the degradation af palmarosa oil. Changes of colour and turbidity was also the evidence for green oil degradation by bacteria. More oxygen included protons (0-CH²) group was produced in the presence of bacterial species and the addition of oxygen took place during bacterial degradation of palmarosa oil. The biodegradation of palmarosa oil by Serratia marcescens have been carried out using High Performance Liquid Chromatography, Fourier Transform Infrared Spectroscopy and Nuclear Magnetic spectroscopy analysis. Carboxyl group present in the palmorasa oil is utilised as a sole carbon sources for the Serratia marcescens.     

Identification of perylene in sediments: Occurrence and diagenetic evolution

Perylene and penta-aromatic hydrocarbons were determined in sediments as part of a study that was dedicated to the aquatic ecosystem of Elelenwo Creek (Southern Nigeria) in order to carry out a critical corroboration of occurrence and diagenetic evolution of perylene in the sediments of the creek. The results show that the annual mean levels of Benzo [g, h, i] Perylene ranged from 209.00–245.28 ?g/kg dry weight at the various stations sampled. Meanwhile, Station 3 recorded the highest mean level of 245.28 ?g/kg dry weight. The observed values for total penta-aromatic hydrocarbons were high (787.00–1154.36?g/kg dry weight) in all the stations sampled. In addition, the highest mean value of 1154.36?g/kg dry weight was again recorded at station 3 for the penta-aromatic hydrocarbons. One origin index or concentration ratio of Ip/Ip+BghiP was also used to evaluate the suitability of the penta-aromatic hydrocarbons as a tracer to distinguish between contaminations arising from different sources. The values for the sampling stations therefore ranged from 0.41 to 0.43. A critical appraisal of the PAH index, consequently, suggested that petroleum combustion is the major penta-aromatic hydrocarbon source in sediments of the creek. The PAH group profile shows that perylene was high in the sediments and would pose apparent effects in fauna. The high concentration of perylene in the sediments was also indicative of an in situ biogenic derivation. Furthermore, a concentration of perylene > 10 % of total penta-aromatic hydrocarbons established a credible diagenetic origin.     

The history of Jonsmod 1981–2006

This is a history of shallow sea modelling developments as viewed through the Jonsmod modelling conferences over the past 25 years. The conferences are reviewed, and what emerges is a coherent progression to present-day modelling. We also see advances in computing and oceanographic observation, although these are, of course, incidental to the modelling from the point of view of these conferences.     

The ortho- to para- ratio of H2 in the starburst of NGC 253

We present measurements of several near-infrared emission lines from the nearby galaxy NGC 253. We have been able to measure four H₂ lines across the circumnuclear starburst, from which we estimate the ortho- to para- ratio of excited H₂ to be ∼2. This indicates that the bulk of the H₂ emission arises from photodissociation regions (PDRs), rather than from shocks. This is the case across the entire region of active star formation.
As the H₂ emission arises from PDRs, it is likely that the ratio of H₂ to Brγ (the bright hydrogen recombination line) is a measure of the relative geometry of O and B stars and PDRs. Towards the nucleus of NGC 253 the geometry is deduced to be tightly clustered O and B stars in a few giant H  II regions that are encompassed by PDRs. Away from the nuclear region, the geometry becomes that of PDRs bathed in a relatively diffuse ultraviolet radiation field.
The rotation curves of 1–0 S(1) and Brγ suggest that the ionized gas is tracing a kinetic system different from that of the molecular gas in NGC 253, particularly away from the nucleus.     

Die fazielle und paläogeographische Entwicklung der infrakambrischen bis ordovizischen Sedimente im Mittleren Antiatlas um Agdz (S-Marokko)

Zusammenfassung Die Entwicklung des Adoudounien (Infrakambrium) und Géorgien (Unterkambrium) ist im Mittleren Antiatlas durch einen Wechsel von marinen und kontinentalen Sedimenten gekennzeichnet. Wildbachablagerungen an der Basis und an den Beckenrändern werden von marin-marginalen stromatolithischen Karbonaten abgelöst. Ignimbrite belegen wiederholte terrestrische Sedimentation.Mit fluviatilen Sanden und wiederum Stromatolithen und lagunären Karbonaten (mit ersten Trilobiten!) setzt ein zweiter transgressiver Großzyklus ein, der an der Wende Infra-/Unter-Kambrium einen ersten Höhepunkt erreicht. Durch regressive Kleinzyklen charakterisierte Abfolgen leiten zu Sandsteinen über, die als Ablagerungen eines Deltas gedeutet werden.Vom Mittelkambrium bis Ordovizium dominiert marine Schelfsedimentation.

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The formations of Adoudounien (Infra Cambrian) and Géorgien (Lower Cambrian) of the middle Anti-Atlas are characterized by an alternation of marine and continental sediments. Torrent conglomerates at the base and the margins of the basin took turns to marine-marginal stromatolitic carbonates. Ignimbrites prove repeated terrestrial sedimentation.A second transgressiv megasequence begins with fluviatil sands and goes on with stromatolites and lagoon carbonates (first Trilobites). This transgression reachs his first culmination at the Infra-/Lower-Cambrian boundary. Typical regressiv cycles form a transition to sandstones, which are interpreted as sediments of a delta.Marine shelf environment dominates from Middle Cambrian to Ordovician beds.

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Résumé Dans le moyen Anti-Atlas, l'évolution de l'Adoudounien et du Géorgien est caractérisée par un changement des sédiments marins et continentaux. Les dépôts des torrents à la base et dans la bordure du bassin font place à des carbonates marins marginaux stromatolithiques. Les ignimbrites marquent le retour fréquent à la sédimentation terrestre.Une deuxième mégaséquence transgressive débute avec des sables fluviatiles, des stromatolithes et des carbonates lagunaires (premiers trilobites). La transgression atteint une première phase culminante à la transition de l'Adoudounien au Géorgien. Des séquences caractérisées par de petits cycles régressifs conduisent à des grès qui pourraient être interpré tés comme des sédiments deltaïques.A partir du Cambrien moyen jusqu'à l'Ordovicien prédomine un milieu de plate-forme externe.

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Adoudounien — — Géorgien — — . — — . , - , , . , , . .

     

Rapid change in early Holocene environments inferred from Lake Pupuke,Auckland City,New Zealand

Sediment cores from Lake Pupuke in Auckland City, New Zealand, contain a high‐resolution millennial to centennial‐scale record of changing climate and catchment hydrology spanning the past ca. 10 000 years. Here, we focus on the period between 9500 ± 25 and 7000 ± 155 cal. yr BP during which grain size, diatom palaeoecology, biogenic silica concentrations, sediment elemental and carbon isotope geochemistry reflect changes in sediment sources and lake conditions, with a significant event commencing at ca. 8240 cal. yr BP, commensurate with a lowering of lake level, faster erosion rates and increased sediment influx with a duration of ca. 360 yrs. However, the changes in the lake are not reflected in the terrestrial vegetation, where the pollen record indicates that podocarp forest dominated the Auckland region, with apparent environmental stability during this part of the early Holocene. The synchronous change in most of the proxies between ca. 8240 and 7880 cal. yr BP at Lake Pupuke indicates the presence of a sustained episode of relatively low lake level and concomitant increased rate of erosion in the early Holocene that appears to be at least partly coeval with the 8200 cal. yr BP meltwater event proposed for the North Atlantic region. Copyright © 2008 John Wiley & Sons, Ltd.     

Shock‐induced changes in density and porosity in shock‐metamorphosed crystalline rocks,Haughton impact structure,Canada

Abstract– Shock metamorphism can occur at transient pressures that reach tens of GPa and well over 1000 °C, altering the target material on both megascopic and microscopic scales. This study explores the effects of shock metamorphism on crystalline, quartzofeldspathic basement material from the Haughton impact structure on Devon Island, Arctic Canada. Shock levels were assigned to samples based on petrographic examination of main mineral phases. Conventional shock classification schemes proved to incompletely describe the Haughton samples so a modified shock classification system is presented. Fifty‐two crystalline bedrock samples from the clast‐rich impact melt rocks in the crater, and one reference site outside of the crater, were classified using this system. The shock levels range from 0 to 7 (according to the new shock stage classification proposed here, i.e., stages 0–IV after the Stöffler classification), indicating shock pressures ranging from 0 to approximately 80 GPa. The second aspect of this study involved measuring bulk physical characteristics of the shocked samples. The bulk density, grain density, and porosity were determined using a water displacement method, a bead displacement method, and a Hepycnometer. Results suggest a nonlinear, negative correlation between density and shock level such that densities of crystalline rocks with original densities of approximately 3 g cm^?3 are reduced to <1.0 g cm^?3 at high shock levels. The results also show a positive nonlinear correlation between porosity and shock level. These data illustrate the effect of shock on the bulk physical characteristics of crystalline rocks, and has implications for assessing the habitability of shocked rocks.     

Precipitation of heavy metals in produced water: influence on contaminant transport and toxicity

Produced water undergoes changes in its physical chemistry including precipitation of heavy metals after being discharged and mixed with ambient seawater. Potential impacts of the precipitation of heavy metals on their transport and toxicity were studied using samples from offshore oil production sites on the Scotian Shelf off eastern Canada. Concentrations of aluminum, cadmium, chromium, cobalt, copper, iron, lead, manganese, nickel and zinc were measured in total, particulate and dissolved fractions together with Microtox tests for assessment of toxicity. Heavy metals in produced water were transformed from dissolved to particulate phase in a period of hours under oxygenated conditions, and aggregated to larger particles that settle rapidly (>100 m/day) over a few days. In addition, there was production of buoyant particles comprised of heavy metal precipitates sequestered onto oil droplets that were transported to the surface. The particulate fraction was generally more toxic than the dissolved fraction. This was evident at the mixing interface between produced water and seawater where elevated particulate and toxicity levels were observed. Laboratory studies suggest an increase in the toxicity of discharged produced water over time. Time-series experiments showed a sustained toxic response for more than a week following the oxidation of freshly discharged produced water that initially elicited little or no toxic response in the Microtox test. Chemical processes identified in this study, namely precipitation of heavy metals and consequent settling and rising fluxes of particles, will influence the toxicity, the fate and the transport of potential contaminants in the produced water. Therefore, these processes need to be considered in assessment of the environmental impact associated with offshore oil and gas operations.     

Study of mango biomass (Mangifera indica L) as a cationic biosorbent

Unfertilizable fruiting buds of mango plant Mangifera Indica L, an agrowaste, is used as a biomass in this study. The efficacy of the biosorbent was tested for the removal of lead, copper, zinc and nickel metal ions using batch experiments in single and binary metal solution under controlled experimental conditions. It is found that metal sorption increases when the equilibrium metal concentration rises. At highest experimental solution concentration used (150 mg/L), the removal of metal ions were 82.76 % for lead, 76.60 % for copper, 63.35 % for zinc and 59.35 % for nickel while at lowest experimental solution concentration (25 mg/L), the removal of metal ions were 92.00% for lead, 86.84 % for copper, 83.96 % for zinc and 82.29 % for nickel. Biosorption equilibrium isotherms were plotted for metal uptake capacity (q) against residual metal concentrations (C_f) in solution. The q versus C_f sorption isotherm relationship was mathematically expressed by Langmuir and Freundlich models. The values of separation factor were between zero and one indicating favourable sorption for four tested metals on the biosorbent. The surface coverage values were approaching unity with increasing solution concentration indicating effectiveness of biosorbent under investigation. The non-living biomass of Mangifera indica L present comparable biosorption capacity for lead, copper, zinc and nickel metal ions with other types of biosorbent materials found in literature and is effective to remove metal ions from single metal solutions as well as in the presence of other co-ions with the main metal of solution.