Volatilization of demethylmercury and elemental mercury from river Elbe floodplain soils

It has been shown that an untreated mercury-polluted floodplain soil (containing 10 μg/g per dry weight (d.w.) total Hg and 12 ng/g (d.w.) monomethylmercury compounds (MMM)) of the river Elbe in Northern Germany contains both dimethylmercury (DMM) and elemental mercury (Hg°). This is the first time ever that DMM has been detected in unmodified soils. A novel purge- and-trap-technique involving a sequential thermodesorption-separation of the two species after trapping on a carbon molecular sieve (CMS) has been developed that allows the determination of the two species DMM and Hg° from aqueous solutions or soil samples by GC-CVAFS. The compounds' identities as Hg-species were confirmed by GC-ICP/MS. A DMM-concentration of 740 pg/g (d.w.) was determined in the soil; the Hg°-concentration was found to be at least four times larger, but could not yet be quantified. Since no precautions against losses via evapoartion were taken during sampling and storage, the original concentrations were probably much higher. Both DMM and Hg° are easily purged with N₂ from soils as well as from soil suspensions, indicating that the two species may readily evaporate from those soils under natural conditions. The amount of DMM determined in the soil suspension was significantly lower (80 pg/g (d.w.)) compared to that in the original soil sample, suggesting that DMM might not be stable under these conditions. Also, it was shown that in natural samples, MMM can be converted into DMM in the presence of sulfide, at S^2?-levels as low as 100 μg/g.     

Design and chemical synthesis of a homogeneous polymer-modified erythropoiesis protein

We report the design and total chemical synthesis of "synthetic erythropoiesis protein" (SEP), a 51-kilodalton protein-polymer construct consisting of a 166-amino-acid polypeptide chain and two covalently attached, branched, and monodisperse polymer moieties that are negatively charged. The ability to control the chemistry allowed us to synthesize a macromolecule of precisely defined covalent structure. SEP was homogeneous as shown by high-resolution analytical techniques, with a mass of 50,825 +/-10 daltons by electrospray mass spectrometry, and with a pI of 5.0. In cell and animal assays for erythropoiesis, SEP displayed potent biological activity and had significantly prolonged duration of action in vivo. These chemical methods are a powerful tool in the rational design of protein constructs with potential therapeutic applications.     

Mercury speciation in contaminated soils by thermal release analysis

Thermal release analysis of mercury species in contaminated soils was performed by temperature controlled continuous heating of the samples in a furnace coupled to an Atomic Absorption Spectrophotometer (AAS). It was shown that this method allows the identification of different redox states of Hg-species through their characteristic releasing temperature ranges. The method was applied to Hg-contaminated samples from an inactive chlor-alkali production plant in former East Germany (GER), and from a gold mining area in Poconé, Mato Grosso, Brazil (BRA), as well as synthetic soil samples obtained by spiking pre-heated soil matrices (GER and BRA) with the following mercury species: Hg⁰, Hg₂Cl₂, HgCl₂, HgO and HgS. The samples GER, in general, frequently showed the presence of Hg²⁺ probably bound to humic substances, in the case of samples with higher total carbon content. Only in highly contaminated samples (>3000 ppm of mercury) was Hg⁰ the predominant species. The samples BRA more frequently showed the presence of mercury species in the lower oxidation states, i.e. Hg¹⁺ in combination with Hg⁰. The method allows observing changes in Hg-speciation in the samples with time, mainly changes among the oxidation states Hg⁰, Hg¹⁺ and Hg²⁺. The treated GER matrix showed a stronger tendency to oxidise Hf-species than the BRA treated matrix, in which only added Hg⁰ is partially oxidised to Hg²⁺ and Hg¹⁺. In contrast, the BRA matrix showed a pronounced tendency to reduce spiked Hg²⁺ to Hg¹⁺. This may be the reason for the presence of Hg¹⁺ in the majority of original BRA samples. The method appears to be very useful to study speciation of mercury and its dynamics. It can be used as a tool for monitoring mercury oxidation states and/or reactions of mercury in soils.     

Energetic particles at venus: galileo results

At Venus the Energetic Particles Detector (EPD) on the Galileo spacecraft measured the differential energy spectra and angular distributions of ions >22 kiloelectron volts (keV) and electrons > 15 keV in energy. The only time particles were observed by EPD was in a series of episodic events [0546 to 0638 universal time (UT)] near closest approach (0559:03 UT). Angular distributions were highly anisotropic, ordered by the magnetic field, and showed ions arriving from the hemisphere containing Venus and its bow shock. The spectra showed a power law form with intensities observed into the 120- to 280-keV range. Comparisons with model bow shock calculations show that these energetic ions are associated with the venusian foreshock-bow shock region. Shock-drift acceleration in the venusian bow shock seems the most likely process responsible for the observed ions.     

Plasma Composition in Jupiter's Magnetosphere: Initial Results from the Solar Wind Ion Composition Spectrometer

The ion composition in the Jovian environment was investigated with the Solar Wind Ion Composition Spectrometer on board Ulysses. A hot tenuous plasma was observed throughout the outer and middle magnetosphere. In some regions two thermally different components were identified. Oxygen and sulfur ions with several different charge states, from the volcanic satellite lo, make the largest contribution to the mass density of the hot plasma, even at high latitude. Solar wind particles were observed in all regions investigated. Ions from Jupiter's ionosphere were abundant in the middle magnetosphere, particularly in the highlatitude region on the dusk side, which was traversed for the first time.     

Mercury and methylmercury in sediments and suspended particles from the river Elbe,North Germany

Total Hg and McHg concentrations have been determined in sediments and suspended particulate matter from one of the most Hg-polluted rivers of the world, the Elbe river in Northern Germany. Results of total Hg and McHg are presented. Total Hg concentrations in suspended particulate matter (SPM) are 30 mg kg^?1 in the average and up to 150 mg kg^?1 as the maximum value. Total Hg-fluxes ^?1 calculated from measurements of an automatically operating station upstream Hamburg as about 17 ta?1 in suspended particles. A new McHg determination by HPLC chromatography and photometric detection was developed and verified. Methylmercury concentrations were up to 10% of the total Hg, i. e. 2.7 mg kg^?1 (dw).     

Sustaining local agriculture Barriers and opportunities to direct marketing between farms and restaurants in Colorado

Research explored methods for shortening the food links or developing the local foodshed by connecting farmers with food service buyers (for restaurants and institutions) in Colorado. Telephone interviews were used to investigate marketing and purchasing practices. Findings include that price is not a significant factor in purchasing decisions; that food buyers prioritize quality as their top purchasing criterion but are not aware that local farmers can provide higher quality, that institutions are interested in buying locally; that small farms can offer comparable or higher quality produce andservice; and that farmers need to show buyers what the quality of produce and service they can provide.     

Mercury contaminated sites — Behaviour of mercury and its species in lysimeter experiments

In a polluted site in Germany not only metallic, ionic and MeHg could be detected, but also organomercurials such as methyl- ethyl- and phenyl-mercury. In addition sometimes other organomercurials could be separated but up to now not identified. Extraction of the organomercurials from soil and percolating water was performed by dithizone, differentiation and detection by High-Performance-Liquid-Chromatography and atomic fluorescence detection, respectively. Differentiation between gaseous organic and gaseous elemental mercury was done by adsorption on Carbotrap^® and gold filters, thermal desorption and detection by atomic fluorescence The behaviour of 8 organomercurials in soil is described. For this a lysimeter of a new design was filled with polluted soil. The top layer of the soil was spiked with 8 organomercurials. The percolating water and the air above the soil, were analyzed. Different layers of the soil were also investigated after the experiment. By synthetic rain the movement of Hg species is low: the compounds stay in the first centimeters. Ethoxyethylmercury⁺, tolylmercury⁺, and nitromersol were not detected in the percocolate. Concentrations of phenylmercury⁺ and hydroxymercurybenzoicacid decreased. Methoxymethylmercury⁺ increased. In the head of the lysimeter, volatile Hg(0) concentration increased during 150 hours by a factor of 5, while volatile organic mercury decreased during this time by a factor of 10. The organomercurial-content in soil decreased.A transformation of organic to inorganic Hg is therefore presumed.     

Assessing the impact of soil amendments made of processed biowaste digestate on soil macrofauna using two different earthworm species

Fermentation in combination with subsequent composting of biowaste is a preferred method for municipalities to recycle organic byproducts and transform them into useful end products for soil amelioration or plant fertilization. These compost products, especially if obtained from household wastes, can be a source of hazardous components, e.g. heavy metals, pathogens, synthetic chemicals or toxic organic compounds. An avoidance test with two earthworm species (Eisenia fetida and Aporrectodea caliginosa) was conducted to assess the impact of differently processed biowaste based digestate products on soil invertebrates. Body weight changes were recorded, as well as differences in effects on adult versus juvenile earthworms.

While E. fetida showed no avoidance towards the digestate products (negative avoidance, meaning that the tested products were preferred, of 80 to 100 %), A. caliginosa rejected the crude biowaste digestate compost in higher concentrations (avoidance of 45 %), but not the agglomerated or pelletized variants. A clear weight gain of up to 25 % was observed only for individuals of E. fetida. The developmental stages of the worms were not crucial for the outcome of the avoidance test.

Based on the results of this study the application of biowaste products on arable land cannot be recommended without constraints.     

Wet-chemical silvering of inert polyethylene terephthalate yarn in a spool dyeing apparatus

Inert polyethylene terephthalate (PET) yarns, which were spooled crosswise onto a cylindrical dyeing bobbin, were silvered successfully with a wet-chemical method by using a newly developed one-bath method on a laboratory scale. In order to characterize the silver coating such as design, homogeneity, and crack formation, the surface morphology (SM) was analyzed using scanning electron microscopy (SEM). The chemical compositions of the surface (percentage of carbon, oxygen, nitrogen, silicium, and silver) were investigated with energy-dispersive x-ray spectroscopy (EDX). Furthermore, the testing of textile-chemical and textile-physical properties such as the washing-fastness, tensile strength, and electrical conductivity was carried out.