Welding fumes from stainless steel gas metal arc processes contain multiple manganese chemical species

Fumes from a group of gas metal arc welding (GMAW) processes used on stainless steel were generated using three different metal transfer modes and four different shield gases. The objective was to identify and measure manganese (Mn) species in the fumes, and identify processes that are minimal generators of Mn species. The robotic welding system was operated in short-circuit (SC) mode (Ar/CO2 and He/Ar), axial spray (AXS) mode (Ar/O2 and Ar/CO2), and pulsed axial-spray (PAXS) mode (Ar/O2). The fumes were analyzed for Mn by a sequential extraction process followed by inductively coupled plasma-atomic emission spectroscopy (ICP-AES) analysis, and by X-ray diffraction (XRD). Total elemental Mn, iron (Fe), chromium (Cr) and nickel (Ni) were separately measured after aqua regia digestion and ICP-AES analysis. Soluble Mn2+, Fe2+, Fe3+, and Ni2+ in a simple biological buffer (phosphate-buffered saline) were determined at pH 7.2 and 5.0 after 2 h incubation at 37 C by ion chromatography. Results indicate that Mn was present in soluble form, acid-soluble form, and acid-soluble form after reduction by hydroxylamine, which represents soluble Mn0 and Mn2+ compounds, other Mn2+ compounds, and (Mn3+ and Mn4+) compounds, respectively. The dominant fraction was the acid-soluble Mn2+ fraction, but results varied with the process and shield gas. Soluble Mn mass percent in the fume ranged from 0.2 to 0.9%, acid-soluble Mn2+ compounds ranged from 2.6 to 9.3%, and acid plus reducing agent-soluble (Mn3+ and Mn4+) compounds ranged from 0.6 to 5.1%. Total Mn composition ranged from 7 to 15%. XRD results showed fumes had a crystalline content of 90-99% Fe3O4, and showed evidence of multiple Mn oxides, but overlaps and weak signals limited identification. Small amounts of the Mn2+ in the fume (<0.01 to ≈ 1% or <0.1 to ≈ 10 microg ml(-1)) and Ni2+ (<0.01 to ≈ 0.2% or <0.1 to ≈ 2 mg ml(-1)) ions were found in biological buffer media, but amounts were highly dependent on pH and the welding process. Mn generation rates for the fractions were tabulated, and the influence of ozone is discussed. The conclusions are that exposures to welding fumes include multiple Mn species, both soluble and insoluble, and that exposures to Mn species vary with specific processes and shield gases.     

Daily temporal structure in African savanna flower visitation networks and consequences for network sampling

Ecological interaction networks are a valuable approach to understanding plant-pollinator interactions at the community level. Highly structured daily activity patterns are a feature of the biology of many flower visitors, particularly provisioning female bees, which often visit different floral sources at different times. Such temporal structure implies that presence/absence and relative abundance of specific flower-visitor interactions (links) in interaction networks may be highly sensitive to the daily timing of data collection. Further, relative timing of interactions is central to their possible role in competition or facilitation of seed set among coflowering plants sharing pollinators. To date, however, no study has examined the network impacts of daily temporal variation in visitor activity at a community scale. Here we use temporally structured sampling to examine the consequences of daily activity patterns upon network properties using fully quantified flower-visitor interaction data for a Kenyan savanna habitat. Interactions were sampled at four sequential three-hour time intervals between 06:00 and 18:00, across multiple seasonal time points for two sampling sites. In all data sets the richness and relative abundance of links depended critically on when during the day visitation was observed. Permutation-based null modeling revealed significant temporal structure across daily time intervals at three of the four seasonal time points, driven primarily by patterns in bee activity. This sensitivity of network structure shows the need to consider daily time in network sampling design, both to maximize the probability of sampling links relevant to plant reproductive success and to facilitate appropriate interpretation of interspecific relationships. Our data also suggest that daily structuring at a community level could reduce indirect competitive interactions when coflowering plants share pollinators, as is commonly observed during flowering in highly seasonal habitats.     

Effects of silver and cerium dioxide micro- and nano-sized particles on Daphnia magna

Acute (96 h) and chronic (21 d) exposures of Daphnia magna neonates were carried out with nano- and micro-sized Ag and CeO(2) particles to assess the influence of both material and size of particles on mortality and moulting. Mortality rates for silver in the acute exposures were: AgNP, 56.7 ± 23.3% at 0.1 mg L(-1) and 100 ± 20% at 1 mg L(-1), and micro-Ag, 13.3 ± 6.7% at 0.1 mg L(-1) and 80 ± 20% at 1 mg L(-1). CeO(2) was not acutely toxic at concentrations up to 10 mg L(-1). Mortality for Ag over 21d at concentrations of up to 0.05 mg L(-1) was low, while mortality of 30% was observed for 0.001 mg L(-1) of nano-Ag. CeO(2), with the exception of the 10 mg L(-1) of nano-CeO(2) (100% mortality by day 7), was non-toxic. Inhibition of moulting and growth in the acute study occurred at toxic concentrations (Ag particles), and at 10 mg L(-1) of nano-CeO(2). The chronic study revealed reduced moulting at 0.001 mg L(-1) of nano-Ag and 0.01 and 0.05 mg L(-1) of both sizes of Ag, but there was no impact on D. magna size, and no effects of CeO(2). The toxicity of nano-CeO(2) may be attributed to reduced feeding and physical interference with the daphnids' carapace, resulting in reduced swimming ability. Our results suggest that Ag NPs in particular have the potential to be harmful to aquatic invertebrates after release into the environment, whereas CeO(2) particles appear to cause little adverse effects, and only at environmentally irrelevant concentrations.     

A Geospatial Methodology to Identify Locations of Concentrated Runoff from Agricultural Fields

A geospatial methodology has been developed that utilizes high resolution lidar‐derived DEMs to help track runoff from agricultural fields and identify areas of potential concentrated flow through vegetated riparian areas in the Coastal Plain of Virginia. Points of concentrated flow are identified across 74 agricultural fields within the Virginia portion of the Chesapeake Bay watershed. On average, 70% of the surface area of the agricultural fields analyzed drains through less than 20 m of the field margin, and on average 81% of the field surface area drains through 1% or less of the field margin. Within the riparian buffer, locations that were predicted by the geospatial model to have high levels of concentrated flow were found to exhibit evidence of channelization. Results indicate that flow concentration and channelized flow through vegetated riparian areas may be common along the margin of agricultural fields, resulting in vegetated riparian areas that are less effective at sediment trapping than assumed. Additional results suggest that the regulations governing the location and width of vegetated riparian may not be sufficient to achieve goals for reducing sediment and nutrient runoff from nonpoint agricultural sources. Combined with the increasing availability of lidar‐derived DEMs, the geospatial model presented has the potential to advance management practices aimed at reducing nonpoint source pollution leaving agricultural fields.     

Manganese-catalyzed degradation of phosphonic acids

The non-biodegradable and chemically very stable phosphonates are used in a variety of industrial applications including cooling waters, oil production and textile industry. We show here that they are degraded in the presence of Mn(II) and oxygen. The half-life for the reaction is 9 min near neutral pH. The presence of other cations such as Ca(II) and Zn(II) considerably slows down the reaction by competition with Mn(II) for the phosphonate. The reaction involves the oxidation of complexed Mn(II) by oxygen to Mn(III) and the subsequent oxidation of phosphonate by Mn(III) thus yielding two stable phosphonic acid breakdown products. The oxidation also proceeds in the presence of the mineral manganite (Mn(III)OOH), and yields the same breakdown products. The use of a newly developed chromatographic method revealed the presence of the breakdown products in wastewater. The results show that manganese-catalyzed oxidation might be an important pathway for phosphonate degradation in natural waters. Electronic Publication     

Inward investment in North‐East England: impact on the market for skills and training

Against a background of inward investment into the region, the paper examines crucial issues relating to labour. It examines approaches to recruitment and the selection process. Skill shortages and strategies for overcoming the problem are analysed together with a consideration about management and managers. The paper concludes with a detailed assessment of policies relating to training.     

Distribution of lead, copper and zinc in size-fractionated river bed sediment in two agricultural catchments of southern Ontario, Canada

Metal (Pb, Cu and Zn) partitioning in six separated sediment size fractions (<8, 8-12, 12-19, 19-31, 31-42, 42-60 microm) of river bed sediment have been analyzed by sequential extraction. The concentrations of some major elements (Si, Al, Ca, Mg, K, Na, Fe, Mn and P), and organic and inorganic C were determined to correlate the elemental composition of the sediment with metal speciation and grain size. Results show that Zn and Pb concentrations increase with decreasing grain size. For Big Creek and Big Otter Creek, respectively, the highest concentrations of Zn (326 and 230 mg kg(-1)) and Pb (158 and 67 mg kg(-1)) were found in the smallest (<8 microm) fraction, whereas the Cu levels (619 and 1281 mg kg(-1)) were most abundant in the second smallest (8-12 microm) fraction. The major accumulative phases for Cu, Zn and Pb were carbonates, Fe/Mn oxides and organic matter, but the relative importance of each phase varied for individual metals and grain sizes. The extraction data show increasing potential bioavailability of metals with decreasing grain size. Estimates of metal yields in the study catchments suggest that over 80% of the metal yield in sediment smaller than 63 microm is associated with solids smaller than 31 microm.     

Studies on plant-mediated fate of the explosives RDX and HMX

The fate of the explosives RDX and HMX on exposure to plants was investigated in 'natural' aquatic systems of Myriophyllum aquaticum for 16 days, and in axenic hairy root cultures of Catharanthus roseus for > or = 9 weeks. Exposure levels were: HMX, 5 mg/l; and RDX, approximately 8 mg/l. Exposure outcomes observed include: HMX, no transformation by aquatic plants, and minimal biological activity by axenic roots; and RDX, removal by both plant systems. In the case of RDX exposure to axenic roots, since 14C-RDX was included, removal was confirmed by the accumulation of 14C-label in the biomass. The intracellular 14C-label in these RDX studies was detected in two forms: intact RDX and bound unknown(s).     

采用大气压电喷雾(API-ESI)质谱和液体样品直接大体积进样技术检测饮用和地下水中的苯基脲类和三嗪类除草剂

本文介绍了大体积进样技术分析一组苯基脲类和三嗪类除草剂多残留的简便方法.