Phosphorus speciation in the sediment and mass balance for the central region of the Great Barrier Reef continental shelf (Australia)

Solid phase P speciation has been determined in sediments from a transect across the central section of the continental shelf and slope of the Great Barrier Reef (GBR) lagoon. This region is characterized by a gradient of riverine aluminosilicate clay and silt nearshore, seawards of which biogenic carbonate sediment predominates. Phosphorus speciation results show large variations along this transect. Organic P and authigenic (apatite) P are the major chemical forms of phosphorus in the central GBR continental shelf sediments. Post-depositional reorganization of P was also observed, converting organic P and iron bound P (Fe-P) to authigenic (apatite) P. Phosphorus burial rate was estimated from measurements of total P concentration and excess ²¹⁰Pb sediment mass accumulation rates. Burial efficiency varies significantly over the shelf. Inshore areas showed significant P remobilization from sediments to the water column (up to ∼50%). The mid and the outer shelf showed little evidence for remobilization (except for coral reef platform sediments), with more of the sediment P being in the less reactive authigenic apatite phases. An appreciable fraction of this non-labile authigenic apatite phase was identified as fish bone. P sources and sinks over the central part of the GBR shelf were quantified using a mass balance approach. This showed that Coral Sea shelf edge upwelling events are essential to satisfy the large P nutrient demand of the whole GBR lagoon. P inputs due to upwelling events were greater than those contributed by local rivers over an average year.     

Preliminary assessment of trace metals and polycyclic aromatic hydrocarbons in the sediments

Total concentrations of Cd, Cr, Co, Fe, Pb, Ni, Mn and Zn were determined by atomic absorption spectrophotometry in the surface sediments of Taylor Creek, Southern Nigeria. The most concentrated trace metals, ranging from 113.2 to 5160.7 mg/g-dry weights were Fe, Pb, Mn, Ni and Zn. There was no significant variation in sediment-associated metal levels (P>0.05). The metal pollution index was highest at Agbia/Nedugo and is attributed to local contamination of the Creek. The concentrations of low molecular weight polycyclic aromatic hydrocarbons (PAHs) were also detected and quantified in the sediments by capillary gas chromatography equipped with a flame ionization detector. The concentration levels of 178.1-1266.3 mg/g-wet weights were high for the PAHs. The results indicate that the pollutants, which are bio-accumulatable, could contribute to inferior biodiversity, and shifts in community composition from sensitive to tolerant taxa.     

Thermodynamic and environmental consideration of advanced gas turbine cycles with reheat and recuperator

The role of gas turbine power plants in electrical energy production has been considerably increased in the last two to three decades. Various methods have been proposed to improve the performance of gas turbine cycles. In this research, two methods, a reheat cycle and a cycle with a reheat and a recuperator, were investigated and compared with a simple cycle. The main objective of this paper is to study the performance of an simple cycle and reheat cycle under actual conditions. In this regard, all processes are treated as actual, and in particular a relatively simple and reliable approach is used to predict the amount of cooling air. The results obtained on the basis of a model developed for this research show that reheating in the context of a realistic study may lead to an improvement both in efficiency and in specific net work using recuperator cause to decrease NOx emission.     

Decolorisation of exhausted reactive dye bath using ozonator for reuse

Exhausted Reactive dye bath samples of Turquoise Blue, Olive Green and Navy Blue shades were collected from cotton knit wear dyeing units in Tirupur. Ozonation was conducted in a column reactor system fed with ozone at the rate of 0.16 g/min to assess its efficiency in reducing the color, chemical oxygen demand and total organic carbon. Complete decolorization of the effluent was achieved in 10 min contact time and ozone consumption of 153 mg/ L for Turquoise Blue, 128 for Olive Green and 143 for Navy Blue shades effluents respectively. The corresponding COD removal was 43%, 44% and 43% for the three shades while TOC removal efficiency was 45%, 45% and 40% respectively. The results from the reusability studies indicate that the dyeing quality was not affected by the reuse of decolorized dye bath for two successive cycles. It is concluded that ozonation is efficient in decolorization of exhausted dye bath effluents containing conventional reactive dyes. However, the corresponding removal of COD from the textile effluent was not significant.     

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.     

Kinetics of copper desorption from soils as affected by different organic ligands

Desorption of Cu and low molecular weight dissolved organics are the primary factors that impact fate and transport of Cu in soils. To improve predictions of the toxicity and threat from Cu contaminated soil, it is critical that time-dependent desorption behavior be understood. In this paper, the effect of organic ligands citrate, malate, and succinate on the kinetics of Cu desorption from contaminated soils varying widely in soil characteristics was investigated at 25° C and the soils used were referred to as clay, calcareous and sandy soils. The amount of Cu released by the used organic ligands varied greatly with physicochemical properties of the soils. The rate of Cu release by different extractants was in the order citric > malic > succinic, which was consistent with the stability constants of Cu complexes with these ligands. The modified Freundlich and the Elovich and Parabolic diffusion models were used to describe dsorption of Cu²⁺ from the three studied soils as affected by the organic ligands. All of the models fit the data well with correlation coefficients ranging from 0.83 to 1.00 (P < 0.01). Each Model has a set of assumptions for the different physical and chemical properties of the systems to which they are being applied. The uses of these equations yield different magnitudes for the calculated variable, but the relationships between the soil + organic ligands and their effect (i.e., increase or decrease) on these variables are the same. Such information is critical, since Cu is used in a variety of industrial and manufacturing processes and is one of the most common contaminants found at hazardous waste sites.     

Carbon monoxide levels along roadway

This paper predicts and compares the carbon monoxide (CO) concentration levels along Sembulan Road for years 2004 and 2014 using CAL3QHC air dispersion model at two major locations, i.e., at Sembulan Roundabout and Sutera Harbour Intersection, Kota Kinabalu, Sabah, Malaysia. The CO concentration “hot-spots” were also identified at Sutera Harbour Intersection, and the highest maximum 1-hr average ground level concentrations of CO modeled for Kpg. Air Sembulan located in the northeast of idling road was 9.33 ppm for year 2004. This study showed that there would be no extreme changes in CO concentration trends for year 2014 although a substantial increase in the number of vehicles is assumed to affect the level of CO concentrations. It was also found that the CO levels would be well below the Malaysian Ambient Air Quality Guidelines of 30 ppm for 1-hour Time-Weighted Average (TWA). Comparisons between the modeled and observed outputs using quantitative data analysis technique and statistical methods indicated that the CAL3QHC predicted results correlated well with measured data. It was predicted that receptors located near to the major intersection, in the long-term would be potentially exposed to relatively higher CO levels.     

Alginate biopolymer production by Azotobacter chroococcum from whey degradation

The potential of three Azotobacter chroococcum strains for whey degradation and alginate production were investigated. After dilution, samples were spread plated on isolation agar and Manitol agar and incubated at 30 °C for 24 h. Microorganisms were screened for their ability to whey degradation and alginate production based on colony morphology, negative and capsule staining, ability to decrease the apparent turbidity of the fermentation broths in batch and semi continuous culture by spectrophotometer assay at 400 nanometer and tensiometer assay. Of the three strains tested for whey degradation, only Azotobacter chroococcum 1723 produced significant apparent growth on whey broth and could decrease about 70 % of turbidity in fermentation broth during 6 days in batch culture. Colonies of this strain was characteristically yellow, large, moucoid and slimy on whey agar than Manitol agar after 24 h at 30 °C. Transmission electron microscopy assay and Carbazole reagent were used to recognize the alginate biopolymer. After optimizing environmental factors such as pH, salt concentration and temperature, this strain was able to produce exopolysaccharide greater than 5 mg/mL. Optimum results were obtained when using whey broth as a fermentation medium without extra salt, temperature at 35 °C and pH 7. Increasing inorganic and organic nitrogen sources (yeast extract and NH₄NO₃) reduced whey degradation at least 30%. Transmission electron microscopy assay showed a net-structured polysaccharide capsule around the cells. Semi-continuous culture results demonstrated that, alginate production as well as whey degradation was decreased (1 mg/mL and 30 %).     

Controlling factors of groundwater hydrochemistry in a small island’s aquifer

Factor analysis was applied to the hydrochemical data set of Manukan Island in order to extract the principal factors corresponding to the different sources of variation in the hydrochemistry. The application of varimax rotation was to ensure the clear definition of the main sources of variation in the hydrochemistry. The geochemical data of dissolved major, minor and trace constituents in the groundwater samples indicates the main processes responsible for the geochemistry evolution. By using Kaiser normalization, principal factors were extracted from the data for each location. The analysis reveals that there are four sources of solutes: (1) seawater intrusion; (2) leaching process of underlying rock mediated by pH; (3) minerals weathering process and (4) dissolution of carbonate minerals characterized by high loadings of Ca, Zn and Mg. Such processes are dominated by the significant role of anthropogenic impact from the over abstraction of fresh water from the aquifer. Those factors contributed to the changes of the groundwater geochemistry behavior explain the effect of rising extraction of freshwater from the aquifer.     

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.