Correlations between forest fires in British Columbia, Canada, and sea surface temperature of the Pacific Ocean

Correlations and cross-correlations between forest fires in the province of British Columbia, Canada, and sea surface temperatures in the Pacific Ocean were evaluated. British Columbia has a long Pacific Ocean coastline; given that there may be teleconnections between the province's forest fires and climate variability over the ocean, significant correlations may exist between forest fires and the sea surface temperature of the Pacific Ocean. Fire occurrences and areas burned through lightning-caused and human-caused fires were analyzed against individual 1° × 1° grid cells of anomalies in the sea surface temperature to determine correlations for the period 1950-2006. Significant correlations (p < 0.05) for vast areas of the ocean were found between occurrences of lightning-caused fires and sea surface temperature anomalies for time lags of 1 and 2 years, whereas significant correlations between occurrences of human-caused fires and sea surface temperature anomalies occurred extensively for many time lags. To support the results of this approach, correlations between fire data and the Niño 3.4, Pacific Decadal Oscillation, and Arctic Oscillation indices were tested for the same period. Significant correlations were found between fire occurrences and these indices at certain time lags. Overall, fire occurrence appeared to be more extensively correlated with sea surface temperature anomalies than was area burned. These results support the hypothesis that teleconnections exist between fire activity in British Columbia and sea surface temperatures in the Pacific Ocean, and the correlations suggest that linear regression models or other regression techniques may be appropriate for predicting fire severity from the sea surface temperatures of one or more previous years.     

Assessment of sociocultural acceptability of biogas from faecal waste as an alternative energy source in selected areas of Benin City,Edo State,Nigeria

Environment, Development and Sustainability - The use of wastes for biogas production has been restricted to few feedstock like cattle manure and food waste. Increasing the feedstock base for...     

Rapid and Low-Cost Method for Evaluation of Nutrient Release from Controlled-Release Fertilizers Using Electrical Conductivity

Methods to determine nutrient release rates of coated fertilizers usually rely on chemical analyses, which often are time-consuming and/or expensive. Our goal was to develop an innovative and rapid low-cost method to evaluate nutrient release from polymer coated MAP or urea using conductometry. The release in water is determined by measuring the electric conductivity (EC) over time, with intervals dependent on release rates. In the case of soluble salt fertilizers, EC can be immediately determined and converted to a concentration using a calibration curve. In the case of urea, an additional step is needed to convert the neutral urea into ammonium. The release rates in water were assessed for a range of commercial and laboratory-coated fertilizers. A validation test demonstrated strong agreement with the release determined using analytical techniques. The EC method hence offers an easy way to quickly evaluate the time course of release of nutrients from controlled-release fertilizers.     

Sub-cooled and flashing liquid jets and droplet dispersion I. Overview and model implementation/validation

Many accidents involve two-phase releases of hazardous chemicals into the atmosphere. This paper describes the results of a third phase of a Joint Industry Project (JIP) on liquid jets and two-phase droplet dispersion. The aim of the project is to increase the understanding of the behaviour of sub-cooled non-flashing and superheated flashing liquid jets, and to improve the prediction of initial droplet size, droplet dispersion and rainout.Phase III of the JIP first included scaled experiments for materials with a range of volatilities (water, cyclohexane, butane, propane and gasoline). These experiments were carried out by Cardiff University including measurements of flow rate and initial droplet size across the full relevant range of superheats. See the companion paper II for further details of these experiments and the derivation of new refined correlations for droplet size distribution and Sauter Mean Diameter. Furthermore large-scale butane experiments were carried out by INERIS (France) to ensure that for more realistic scenarios the derived droplet size correlations are accurate.Model validation and model improvements were carried out by DNV Software, including validation of release rate and initial droplet size against the above scaled and large-scale experiments. New correlations for droplet size distribution and Sauter Mean Diameter (SMD) were implemented into the Phast discharge model. These were compared against a range of other droplet size and rainout correlations published in the literature, in conjunction with validation against an extensive set of experiments. It was shown that the new droplet size correlation agrees better against experimental data than the existing Phast correlation. To further improve the rainout prediction, the Phast dispersion model (UDM) was also extended to allow simultaneous modelling of a range of droplet sizes and distributed rainout (rather than rainout at one point).     

Wet deposition of mercury within the vicinity of a cement plant before and during cement plant maintenance

Hg species (total mercury, methylmercury, reactive mercury) in precipitation were investigated in the vicinity of the Lehigh Hanson Permanente Cement Plant in the San Francisco Bay Area, CA., USA. Precipitation was collected weekly between November 29, 2007 and March 20, 2008, which included the period in February and March 2008 when cement production was minimized during annual plant maintenance. When the cement plant was operational, the volume weighted mean (VWM) and wet depositional flux for total Hg (Hg_T) were 6.7 and 5.8 times higher, respectively, compared to a control site located 3.5 km east of the cement plant. In February and March, when cement plant operations were minimized, levels were approximately equal at both sites (the ratio for both parameters was 1.1). Due to the close proximity between the two sites, meteorological conditions (e.g., precipitation levels, wind direction) were similar, and therefore higher VWM Hg_T levels and Hg_T deposition likely reflected increased Hg emissions from the cement plant. Methylmercury (MeHg) and reactive Hg (Hg(II)) were also measured; compared to the control site, the VWM for MeHg was lower at the cement plant (the ratio = 0.75) and the VWM for Hg(II) was slightly higher (ratio = 1.2), which indicated the cement plant was not likely a significant source of these Hg species to the watershed.     

Media Representations of Climate Change: A Meta-Analysis of the Research Field

A flurry of studies in recent years has analyzed the role of media in climate change communication. This article provides a systematic, large-scale, and up-to-date overview of the objects and characteristics of this research field through a meta-analysis. It identifies 133 relevant studies and analyzes them empirically. The results show that research activity has risen strongly over time, and that the analytical spectrum has expanded to include an increasing number of countries, more types of media including online and social media, and different methodological approaches. The analysis also demonstrates, however, that scholarship in the field still concentrates strongly on Western countries and print media.     

Unleaded Gasoline Shortages and Fuel Switching

The use of leaded gasoline in automobiles equipped with catalytic converters causes deactivation of the converters and leads to significant increases in emissions of reactive hydrocarbons, a precursor of ozone. Such fuel switching may be a contributing factor to the increase in photochemical smog levels recently observed in the South Coast Air Basin (SOCAB).     

Human health effects of residual carbon nanotubes and traditional water treatment chemicals in drinking water

The volume of industrial and domestic wastewater is increasing significantly year by year with the change in the lifestyle based on mass consumption and mass disposal brought about by the dramatic development of economies and industries. Therefore, effective advanced wastewater treatment is required because wastewater contains a variety of constituents such as particles, organic materials, and emulsion depending on the resource. However, residual chemicals that remain during the treatment of wastewaters form a variety of known and unknown by-products through reactions between the chemicals and some pollutants. Chronic exposure to these by-products or residual chemicals through the ingestion of drinking water, inhalation and dermal contact during regular indoor activities (e.g., showering, bathing, cooking) may pose cancer and non-cancer risks to human health. For example, residual aluminium salts in treated water may cause Alzheimer's disease (AD). As for carbon nanotubes (CNTs), despite their potential impacts on human health and the environment having been receiving more and more attention in the recent past, existing information on the toxicity of CNTs in drinking water is limited with many open questions. Furthermore, though general topics on the human health impacts of traditional water treatment chemicals have been studied, no comparative analysis has been done. Therefore, a qualitative comparison of the human health effects of both residual CNTs and traditional water treatment chemicals is given in this paper. In addition, it is also important to cover and compare the human health effects of CNTs to those of traditional water treatment chemicals together in one review because they are both used for water treatment and purification.