Duetting and mate-guarding in Australian magpie-larks (Grallina cyanoleuca)

A recently favored hypothesis is that duetting in birds has a mate-guarding function: a male responds vocally to his partner’s song, thereby forming a duet that repels males who are attracted to her song. Previous studies have not provided unambiguous tests of the mate-guarding hypothesis because: (1) the probability of a male answering his partner’s song has not been shown to increase specifically when the female is fertile, and (2) the probability of a male answering his partner’s song has not been assessed separately from simply a higher song initiation rate. We investigated extra-pair paternity, mate-guarding, and duetting in the socially monogamous Australian magpie-lark (Grallina cyanoleuca). DNA fingerprinting revealed that 3% of young were the result of extra-pair paternity, and we found that males guarded fertile females by staying close to them. However, males did not initiate songs at a higher rate when females were fertile and actually reduced their probability of replying to female song during this period. We conclude that although male magpie-larks did guard fertile females in an attempt to prevent extra-pair copulations, they did not use duetting for this purpose. Received: 10 May 1999 / Received in revised form: 27 September 1999 / Accepted: 2 October 1999     

Aerial measurement of radioxenon concentration off the west coast of Vancouver Island following the Fukushima reactor accident

In response to the Fukushima nuclear reactor accident, on March 20th, 2011, Natural Resources Canada conducted aerial radiation surveys over water just off the west coast of Vancouver Island. Dose-rate levels were found to be consistent with background radiation, however a clear signal due to ¹³³Xe was observed. Methods to extract ¹³³Xe count rates from the measured spectra, and to determine the corresponding ¹³³Xe activity concentration, were developed. The measurements indicate that ¹³³Xe concentrations on average lie in the range of 30-70 Bq/m³.     

Increase in Hair Lead, but not Blood Lead Content of Occupationally-Exposed Workers

This study attempted to investigate whether increased hair lead concentrations due to environmental exposure are accompanied by parallel increases in blood lead concentrations. A sample set consisting of both occupationally-exposed individuals and persons from the general population was investigated. The lead content of scalp and pubic hair from the general population (n=189), traffic police personnel (n=27) and battery workers (n=22) were analysed. The hair samples were taken from the nape of the neck by cutting 23 cm closest to the scalp and cleaned using a washing procedure developed in our laboratory. The effectiveness of the washing procedure was partly determined by examining the scanning electron micrographs of the hair samples. Venous samples of blood were taken from each volunteer's arm.The traffic police and battery plant operators sampled had significantly higher average scalp hair and pubic hair lead levels than the non occupationally-exposed general population. No significant differences were found between the blood lead values of these workers and the general population. Compared to the general population both occupationally-exposed groups had significantly more symptoms of lead toxicity.Lead particles were still observed on the hair shafts after the washing procedure. The amount of such lead contamination was difficult to quantify, the problem being further exacerbated by the difference in hair texture of the persons sampled. This exogenous contamination therefore detracts from the usefulness of hair as an indicator of lead exposure.     

Stationary Combustion NOX Control A Summary of the 1989 Symposium

This paper summarizes information and results presented at the 1989 Symposium on Stationary Combustion NOX Control, held March 6-9, 1989 in San Francisco. Cosponsored by the Electric Power Research Institute (EPRI) and the U.S. Environmental Protection Agency, (EPA) the symposium was the fifth in a biennial series.     

Predicting the Performance of VOC Condensers

Volatile organic compounds (VOC) are commonly released from process vents and equipment leaks. These discharges are a threat to the environment, and cost manufacturers millions of dollars in added raw material costs. For these reasons, one may be confronted with the task of evaluating alternatives for reducing VOC emissions from a process plant.

There are two basic approaches for reducing VOC emissions: a) changing the process, or b) installing control equipment.

Methods for changing the process include replacing highly volatile solvents with less volatile ones, making piping changes to reduce the number of vents, tightening the process to eliminate open tanks and leaks, altering process temperature and pressure conditions, etc. Equipment that is applicable to VOC emission control includes incineration, carbon adsorption, scrubbing and condensation.

This article addresses the application of condensers to process vents. A computer spreadsheet model is described, providing a quick screening which indicates whether a vent condenser might be a viable option for controlling emissions. The template provides, for each of a range of condensing temperatures, estimates for the amount of VOC that will be condensed, the condenser size and the tons of refrigeration required.     

Wetlands as principal zones of methylmercury production in southern Louisiana and the Gulf of Mexico region

It is widely recognized that wetlands, especially those rich in organic matter and receiving appreciable atmospheric mercury (Hg) inputs, are important sites of methylmercury (MeHg) production. Extensive wetlands in the southeastern United States have many ecosystem attributes ideal for promoting high MeHg production rates; however, relatively few mercury cycling studies have been conducted in these environments. We conducted a landscape scale study examining Hg cycling in coastal Louisiana (USA) including four field trips conducted between August 2003 and May 2005. Sites were chosen to represent different ecosystem types, including: a large shallow eutrophic estuarine lake (Lake Pontchartrain), three rivers draining into the lake, a cypress-tupelo dominated freshwater swamp, and six emergent marshes ranging from a freshwater marsh dominated by Panicum hemitomon to a Spartina alterniflora dominated salt marsh close to the Gulf of Mexico. We measured MeHg and total Hg (THg) concentrations, and ancillary chemical characteristics, in whole and filtered surface water, and filtered porewater. Overall, MeHg concentrations were greatest in surface water of freshwater wetlands and lowest in the profundal (non-vegetated) regions of the lake and river mainstems. Concentrations of THg and MeHg in filtered surface water were positively correlated with the highly reactive, aromatic (hydrophobic organic acid) fraction of dissolved organic carbon (DOC). These results suggest that DOC plays an important role in promoting the mobility, transport and bioavailability of inorganic Hg in these environments. Further, elevated porewater concentrations in marine and brackish wetlands suggest coastal wetlands along the Gulf Coast are key sites for MeHg production and may be a principal source of MeHg to foodwebs in the Gulf of Mexico. Examining the relationships among MeHg, THg, and DOC across these multiple landscape types is a first step in evaluating possible links between key zones for Hg(II)-methylation and the bioaccumulation of mercury in the biota inhabiting the Gulf of Mexico region.     

Effect of decabromodiphenyl ether and antimony trioxide on controlled pyrolysis of high-impact polystyrene mixed with polyolefins

The controlled pyrolysis of polyethylene/polypropylene/polystyrene mixed with brominated high-impact polystyrene containing decabromodiphenyl ether as a brominated flame-retardant with antimony trioxide as a synergist was performed. The effect of decabromodiphenyl ether and antimony trioxide on the formation of its congeners and their effect on distribution of pyrolysis products were investigated. The controlled pyrolysis significantly affected the decomposition behavior and the formation of products. Analysis with gas chromatograph with electron capture detector confirmed that the bromine content was rich in step 1 (oil 1) liquid products leaving less bromine content in the step 2 (oil 2) liquid products. In the presence of antimony containing samples, the major portion of bromine was observed in the form of antimony bromide and no flame-retardant species were found in oil 1. In the presence of synergist, the step 1 and step 2 oils contain both light and heavy compounds. In the absence of synergist, the heavy compounds in step 1 oil and light compounds in step 2 oils were observed. The presence of antimony bromide was confirmed in the step 1 oils but not in step 2 oils.