Algal overgrowth of alcyonacean soft corals

Colonies of the soft coral Lobophytum pauciflorum (Ehrenberg, 1834) (Coelenterata: Octocorallia: Alcyonacea: Alcyoniidae), some of which were heavily overgrown by the algae Ceranium flaccidum (Kuetzing) Ardissone and Enteromorpha sp., and other minor epizoites, were collected at Taylor Reef (17°50S; 146°35E) in the Great Barrier Reef. Overgrown colonies contained the diterpene 2-epi-sarcophytoxide as the major secondary metabolite, while conspecific colonies with clean polyparies contained two diterpenes in approximately equal amounts: 14-hydroxycembra-1,3,7,11-tetraene and 15-hydroxycembra-1,3,7,11-tetraene. By contrast, twenty conspecific pairs of overgrown and clean colonies of other alcyoniid soft corals collected from Pelorus Channel, Palm Island Group (18°34S; 146°29E), showed no chemical differences within in the pairs. Cultures of a common species of Ceramium [C. codii (Richards) Mazoyer] were incubated with different concentrations of nine soft-coral-derived diterpenes and significant algal growth inhibition was observed in many cases. It appears that terpenoids from soft coral may contribute to the lack of epizoic organisms on soft-coral polyparies.     

Airborne emissions of mercury from municipal solid waste. II: potential losses of airborne mercury before landfill

Waste distribution and compaction at the working face of municipal waste landfills releases mercury vapor (Hg(o)) to the atmosphere, as does the flaring of landfill gas. Waste storage and processing before its addition to the landfill also has the potential to release Hg(o) to the air if it is initially present or formed by chemical reduction of Hg(II) to Hg(o) within collected waste. We measured the release of Hg vapor to the atmosphere during dumpster and transfer station activities and waste storage before landfilling at a municipal landfill operation in central Florida. We also quantified the potential contribution of specific Hg-bearing wastes, including mercury (Hg) thermometers and fluorescent bulbs, and searched for primary Hg sources in sorted wastes at three different landfills. Surprisingly large fluxes were estimated for Hg losses at transfer facilities (approximately 100 mg/hr) and from dumpsters in the field (approximately 30 mg/hr for 1000 dumpsters), suggesting that Hg emissions occurring before landfilling may constitute a significant fraction of the total emission from the disposal/landfill cycle and a need for more measurements on these sources. Reducing conditions of landfill burial were obviously not needed to generate strong Hg(o) signals, indicating that much of the Hg was already present in a metallic (Hg(o)) form. Attempts to identify specific Hg sources in excavated and sorted waste indicated few readily identifiable sources; because of effective mixing and diffusion of Hg(o), the entire waste mass acts as a source. Broken fluorescent bulbs and thermometers in dumpsters emitted Hg(o) at 10 to >100 microg/hr and continued to act as near constant sources for several days.     

Airborne emissions of mercury from municipal solid waste. I: new measurements from six operating landfills in Florida

Mercury-bearing material enters municipal landfills from a wide array of sources, including fluorescent lights, batteries, electrical switches, thermometers, and general waste; however, the fate of mercury (Hg) in landfills has not been widely studied. Using automated flux chambers and downwind atmospheric sampling, we quantified the primary pathways of Hg vapor releases to the atmosphere at six municipal landfill operations in Florida. These pathways included landfill gas (LFG) releases from active vent systems, passive emissions from landfill surface covers, and emissions from daily activities at each working face (WF). We spiked the WF at two sites with known Hg sources; these were readily detected downwind, and were used to test our emission modeling approaches. Gaseous elemental mercury (Hg(O)) was released to the atmosphere at readily detectable rates from all sources measured; rates ranged from approximately 1-10 ng m(-2) hr(-1) over aged landfill cover, from approximately 8-20 mg/hr from LFG flares (LFG included Hg(O) at microg/m3 concentrations), and from approximately 200-400 mg/hr at the WF. These fluxes exceed our earlier published estimates. Attempts to identify specific Hg sources in excavated and sorted waste indicated few readily identifiable sources; because of effective mixing and diffusion of Hg(O), the entire waste mass acts as a source. We estimate that atmospheric Hg releases from municipal landfill operations in the state of Florida are on the order of 10-50 kg/yr, substantially larger than our original estimates, but still a small fraction of current overall anthropogenic losses.     

Potential effects of UV-B on the chemical environment of marine organisms: a review

An increase in ultraviolet-B (UV-B) due to depletion of stratospheric ozone may affect growth of marine phytoplankton by altering the chemistry of their environment. Production of bioactive free radicals, photodecomposition of organic matter, and availability of trace metals are likely to be altered by increased UV-B flux. Such changes to the chemical environment may be both deleterious and beneficial to marine phytoplankton. Extracellular free radicals such as OH, Br(2)(-), and CO(3)(-) are predicted to have a negligible impact, but superoxide and its decomposition product hydrogen peroxide may react rapidly with cell surfaces and destroy membrane function and integrity. Increased UV-B will enhance the bioavailability of the redox active trace metals Fe and Cu. Thus, in the Fe-limited high latitude ocean, increased Fe availability may promote phytoplankton production, while in other parts of the ocean increased Cu availability may be toxic. Overall, the interdependent direct and indirect effects of UV-B on phytoplankton may compensate for each other and account for the ability of marine ecosystems to be subjected to widely variable UV-B flux without apparent damage.     

A case study on the influence of a magnetic shielding retrofit on the static magnetic field present in a Magnetic Resonance Imaging (MRI) suite

PurposeThe purpose of this research is to assess whether the practice of retro-fitting passive magnetic shielding to Magnetic Resonance Imaging (MRI) suites is effective in retaining the 0.5 mT footprint of the static magnetic field to within its designed position.MethodologyThe research methodology involved identification of an MRI installation where passive magnetic shielding was to be fitted to an installation already in operational use. Site based physical measurements of the magnetic flux density of the static field were then taken both ante and post installation of the shielding, so as to be able to determine its effectiveness.FindingsThe results identified areas in the retrofitted magnetic shielding where, as a result of its design, hot spots in excess of 0.5 mT occurred.Practical implicationsThis research highlights design, construction and safety issues that the designer could, if he had this prior knowledge, have eliminated at source.ValueAt the planning stage of a new MRI suite, designers could use the information contained in this research as part of their design risk management process. This research serves to demonstrate the importance of eliminating any possible future need to install retrofitted passive magnetic shielding to an original MRI suite design. It also shows the need for designers to identify the location of any hot spots in the shielding installation where the magnetic flux density may exceed 0.5 mT and become a potential hazard to those individuals fitted with heart pacemakers or other electronic body implants.     

Comparative Water Quality of Lightly- and Moderately-Impacted Streams in the Southern Blue Ridge Mountains, USA

For less-developed regions like the Blue Ridge Mountains, data are limited that link basin-scale land use with stream quality. Two pairs of lightly-impacted (90–100% forested) and moderately-impacted (70–80% forested) sub-basins of the upper Little Tennessee River basin in the southern Blue Ridge were identified for comparison. The pairs contain physically similar stream reaches, chosen for the purpose of isolating forest conversion as a potential driver of any detected differences in water quality. Streams were sampled during baseflow conditions twice monthly over a six-month period from September 2003 through February 2004. Parametric t-tests were run for each parameter measured between the lightly-and moderately-impacted streams within each pair. Statistically significantly higher mean values of suspended and dissolved solids, nitrate, specific conductivity, turbidity, and temperature were observed in the moderately impacted streams versus the lightly impacted streams in both pairs, while dissolved oxygen levels were lower in the moderately-impacted streams. No significant differences were demonstrated in orthophosphate or ammonium concentration. A near-bankfull runoff event on February 6, 2004, was sampled for stormflow values, and the results support baseflow findings. The water quality of these streams is very good when compared with lower relief areas like the Piedmont, and none of the parameters measured in this study exceeds levels of known threat to stream biota. However, the demonstration that moderate reductions in forest cover are associated with stream water quality degradation carries important implications for stream management in this rapidly developing mountainous region.     

Monitoring of atrazine in milk using a rapid tube-based ELISA and validation with HPLC

Although atrazine has been banned in the European Union since 2007 it still persists in soil from where it can enter the food chain. Milk-producing animals accumulate atrazine from contaminated feed and water and since large quantities of milk and milk products are consumed its quality should be constantly monitored. The objective of this investigation was to develop a simple tube ELISA procedure suitable for use in non-specialised laboratories and in the field. A polyclonal antibody raised in sheep and the hapten-gelatine conjugate was immobilised onto polystyrene tubes. This enables the colour produced to be read on a basic spectrophotometer. Milk samples were collected from three farms in different regions of Poland and diluted before immunoassay was performed. Samples were extracted with hexane-acetone for HPLC analysis. The amount of fat in the milk samples interferes with the dose response so it essential that the standards are prepared in the same samples matrix. A good correlation between 1% and 2% was found between the two methods in the analysis of real samples. However the ELISA procedure was more sensitive that the HPLC method since atrazine was detected in some samples by the ELISA but was not confirmed by the HPLC method. The study demonstrated that the simple antigen-coated tube assay provides a cost effective and valuable screening test that can be easily modified for direct use as a screening tool in the field.     

Estimating the spatial scale of herbicide and soil interactions by nested sampling, hierarchical analysis of variance and residual maximum likelihood

An unbalanced nested sampling design was used to investigate the spatial scale of soil and herbicide interactions at the field scale. A hierarchical analysis of variance based on residual maximum likelihood (REML) was used to analyse the data and provide a first estimate of the variogram. Soil samples were taken at 108 locations at a range of separating distances in a 9 ha field to explore small and medium scale spatial variation. Soil organic matter content, pH, particle size distribution, microbial biomass and the degradation and sorption of the herbicide, isoproturon, were determined for each soil sample. A large proportion of the spatial variation in isoproturon degradation and sorption occurred at sampling intervals less than 60 m, however, the sampling design did not resolve the variation present at scales greater than this. A sampling interval of 20-25 m should ensure that the main spatial structures are identified for isoproturon degradation rate and sorption without too great a loss of information in this field.