Mortality of large trees and lianas following experimental drought in an Amazon forest

Severe drought episodes such as those associated with El Ni?o Southern Oscillation (ENSO) events influence large areas of tropical forest and may become more frequent in the future. One of the most important forest responses to severe drought is tree mortality, which alters forest structure, composition, carbon content, and flammability, and which varies widely. This study tests the hypothesis that tree mortality increases abruptly during drought episodes when plant-available soil water (PAW) declines below a critical minimum threshold. It also examines the effect of tree size, plant life form (palm, liana, tree) and potential canopy position (understory, midcanopy, overstory) on drought-induced plant mortality. A severe, four-year drought episode was simulated by excluding 60% of incoming throughfall during each wet season using plastic panels installed in the understory of a 1-ha forest treatment plot, while a 1-ha control plot received normal rainfall. After 3.2 years, the treatment resulted in a 38% increase in mortality rates across all stems >2 cm dbh. Mortality rates increased 4.5-fold among large trees (>30 cm dbh) and twofold among medium trees (10-30 cm dbh) in response to the treatment, whereas the smallest stems were less responsive. Recruitment rates did not compensate for the elevated mortality of larger-diameter stems in the treatment plot. Overall, lianas proved more susceptible to drought-induced mortality than trees or palms, and potential overstory tree species were more vulnerable than midcanopy and understory species. Large stems contributed to 90% of the pretreatment live aboveground biomass in both plots. Large-tree mortality resulting from the treatment generated 3.4 times more dead biomass than the control plot. The dramatic mortality response suggests significant, adverse impacts on the global carbon cycle if climatic changes follow current trends.     

Ferrate(VI): green chemistry oxidant for degradation of cationic surfactant

Iron in its familiar form exists in the +2 and +3 oxidation states, however, higher oxidation state of iron +6, ferrate(VI) (Fe(VI)O(4)(2-)) can be obtained. The high oxidation power of ferrate(VI) can be utilized in developing cleaner ("greener") technology for remediation processes. This paper demonstrates the unique property of ferrate(VI) to degrade almost completely the cationic surfactant, cetylpyridinium chloride (C(5)H(5)N(+)(CH(2))(15)CH(3).H(2)O Cl(-), CPC). The Rate law for the oxidation of CPC by ferrate(VI) at pH 9.2 was found to be: -d[Fe(VI)]/dt = k[Fe(VI)][CPC](2). Ferrate(VI) oxidizes CPC within minutes and molar consumption of ferrate(VI) was nearly equal to the oxidized CPC. The decrease in total organic carbon (TOC) from CPC was more than 95%; suggesting mineralization of CPC to carbon dioxide. Ammonium ion was the other product of the oxidation. This is the first report in which Fe(VI)O(4)(2-) ion opens the pyridine ring and mineralizes the aliphatic chain of the organic molecule giving inorganic ions.     

Sediment deposition rate in the Falefa River basin, Upolu Island, Samoa

The (137)Cs method was employed to investigate the recent historical rate of sediment deposition on a lowland alluvial floodplain in the Falefa River basin, Upolu Island, Samoa. Caesium stratigraphy in the floodplain sediment profile was clearly defined, with a broad peak at 145-175 cm depth. The measured rate of vertical accretion over the last 40 years is 4.0+/-0.4 cm per year. This rate exceeds observations in humid environments elsewhere, but is similar to that recorded on other tropical Pacific Islands. Available flow data for the Vaisigano River in Samoa give a 'near-catastrophic' index value of 0.6 for flood variability. This is associated with the occurrence of tropical cyclones and storms in the Samoa area. Large floods therefore probably contribute to the high rate of floodplain sedimentation on Upolu Island. A small but growing body of evidence suggests that fluvial sedimentation rates on tropical Pacific islands are some of the highest in the world.     

The deployment of an advanced gasification technology in the treatment of household and other waste streams

The Gasplasma^® process developed by APP is an advanced thermal conversion (ATC) technology which has been developed for the treatment of household and trade wastes and has also been successfully applied to the handling of wastes derived from landfill and would be capable of achieving effective energy conversion when utilised as an integrated part of the Enhanced Landfill Mining (ELFM) concept.The core Gasplasma^® technology comprises a two-stage thermal treatment system—firstly, a fluidizing bed gasifier which converts the wastes to a crude syngas using oxy-steam and, secondly, a plasma converter that efficiently cracks problematic tars in the raw syngas to produce a reformed and clean syngas suitable for generating electrical power in gas engines and also recovering an environmentally stable vitrified product for use as a secondary aggregate material. The utilization of oxy-steam as a gasifying agent greatly reduces the syngas volume compared to other ATC processes and incineration and hence reduces the cost of the gas cleaning system while improving the efficiency of the process. By adopting this two-stage approach, high energy conversion (74–90%) and carbon conversion (95 ± 1.6%) efficiencies were achieved with the Gasplasma^® plant that compare favourably with published efficiencies data. The calculated net exportable power generation efficiency for a commercial scale plant is significantly in excess of 25%. This compares well with the published figures of 17.7–23% for fluidized bed technologies processing MSW.     

Bromate analysis in groundwater and wastewater samples

Bromate (BrO(3)(-)) is a disinfection by-product formed during ozonation of potable water supplies containing bromide (Br(-)). Bromate has been classed by the World Health Organisation as a 'possible human carcinogen', leading to implementation of 10-25 microg L(-1)(as BrO(3)(-)) drinking water limits in legislative areas including the United States and European Union. Techniques have been developed for bromate analysis at and below regulatory limits, with Ion Chromatography (IC) coupled with conductivity detection (IC-CD), post-column reaction and ultra-violet (UV) detection (IC-PCR), or inductively coupled plasma-mass spectrometry detection (IC-ICPMS) in widespread use. The recent discovery of bromate groundwater contamination in a UK aquifer has led to a requirement for analysis of bromate in a groundwater matrix, for environmental monitoring and development of remediation strategies. The possibility of bromate-contaminated water discharge into sewage treatment processes, whether accidental or as a pump-and-treat strategy, also required bromate analysis of wastewater sources. This paper summarises techniques currently available for trace bromate analysis in potable water systems and details studies to identify a methodology for routine analysis of groundwater and wastewater samples. Strategies compared were high performance liquid chromatography (HPLC) with direct UV or PCR/UV detection, IC-CD, IC-PCR, and a simple spectrophotometric technique. IC-CD was the most cost-effective solution for simultaneous analysis of bromate and bromide within groundwater samples, having a 5 microg L(-1) detection limit of both anions with limited interference from closely-eluting species. Wastewater samples were successfully analysed for bromate only using HPLC with PCR/UV detection, with detection limits below 20 microg L(-1)(as BrO(3)(-)) and low interference. HPLC with direct UV detection was unsuitable for bromate analysis within the concentration range 50-5000 microg L(-1) which was required for this project, but column choice was shown to be a major factor in determining limits of detection. Spectrophotometry could not reproducibly determine bromate concentration, although the technique showed promise as a quick field method for high-level groundwater bromate analysis.     

Phosphorus concentrations in overland flow from diverse locations on a New York dairy farm

The National Phosphorus Project rainfall simulator was used to quantify overland flow and P transport from nine sites distributed throughout the watershed of a New York City Watershed Agriculture Program collaborating dairy farm. Observed concentrations of total dissolved phosphorus (TDP) were low (0.007-0.12 mg L(-1)) in flow from deciduous forest, extensively managed pasture, and hillside seeps; moderate (0.18-0.64 mg L(-1)) in flow from intensively managed pastures, a hayfield, and a cow path; and extremely high (11.6 mg L(-1)) in flow from a manured barnyard. Concentrations of TDP from sites without fresh manure were strongly correlated with soil test P (TDP [mg L(-1)] = 0.0056 + 0.0180 x Morgan's soil test phosphorus [STP, mg kg(-1)]; R2 = 84%). Observed concentrations of suspended solids were low (16-137 mg L(-1)) in flow from vegetated sites, but were higher (375-615 mg L(-1)) in flow from sites with little ground cover (barnyard, cow path, plowed field). Under dry summer conditions the time to observed overland flow was shorter (<18 min) for nonfield areas (seeps, barnyard, cow path) than for field and forest areas (27-93 min), indicating that hydrologically active nonfield areas of minor spatial extent but with high soil P (e.g., cow paths and barnyards) can play a significant role in summertime P loading. When soils started from field capacity (second-day) time to overland flow was uniformly less than 23 min, indicating that under wet watershed conditions low-P source areas can dilute overland flow from concentrated sources.     

Studies into the formation of dioxins in the sintering process used in the iron and steel industry. 1. Characterisation of isomer profiles in particulate and gaseous emissions

Dioxin analyses using a DB5MS chromatography column are presented for samples of dust from an electrostatic precipitator and emissions from the main stack of a UK sinter plant. The analyses have been repeated using the SP2331 column, for which the elution order has been determined for the whole range of tetra to octachlorodibenzo-p-dioxins and dibenzofurans, and which provides a larger degree of separation than the DB5MS column. Polychlorinated dibenzofurans are present in significantly larger amounts in both the dust and stack emissions, and are the main contributors to the I-TEQ. Analysis using the SP2331 column for dioxins show considerable similarity to those of Bacher et al. for soot from a wood-burning fire, but differ markedly from those of Addink et al. for simulation of waste incineration. The similarities to Bacher's results are less for the dibenzofurans. Comparison of absolute concentrations with reported vapour pressures shows the retention of significant dioxin in the dust to involve mechanisms other than pure condensation.