41 research outputs found

    Species and Genotype Effects of Bioenergy Crops on Root Production, Carbon and Nitrogen in Temperate Agricultural Soil

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    Bioenergy crops have a secondary benefit if they increase soil organic C (SOC) stocks through capture and allocation below-ground. The effects of four genotypes of short-rotation coppice willow (Salix spp., ‘Terra Nova’ and ‘Tora’) and Miscanthus (M. × giganteus (‘Giganteus’) and M. sinensis (‘Sinensis’)) on roots, SOC and total nitrogen (TN) were quantified to test whether below-ground biomass controls SOC and TN dynamics. Soil cores were collected under (‘plant’) and between plants (‘gap’) in a field experiment on a temperate agricultural silty clay loam after 4- and 6-years’ management. Root density was greater under Miscanthus for plant (up to 15.5 kg m–3) compared with gap (up to 2.7 kg m–3) whereas willow had lower densities (up to 3.7 kg m–3). Over two years, SOC increased below 0.2 m depth from 7.1 to 8.5 kg m–3 and was greatest under Sinensis at 0-0.1 m depth (24.8 kg m–3). Miscanthus-derived SOC, based on stable isotope analysis, was greater under plant (11.6 kg m–3) than gap (3.1 kg m–3) for Sinensis. Estimated SOC stock change rates over the two-year period to 1-m depth were 6.4 for Terra Nova, 7.4 for Tora, 3.1 for Giganteus and 8.8 Mg ha–1 year–1 for Sinensis. Rates of change of TN were much less. That SOC matched root mass down the profile, particularly under Miscanthus, indicated that perennial root systems are an important contributor. Willow and Miscanthus offer both biomass production and C sequestration when planted in arable soil

    Sewage sludge treated with metal nanomaterials inhibits earthworm reproduction more strongly than sludge treated with metal metals in bulk/salt forms

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    Earthworms were exposed to soils amended with sewage sludges from a wastewater treatment plant (WWTP) treated with nanomaterials (ENMs) or metal/ionic salts. Sewage sludges were generated with either no metal added to the WWTP influent (control), ionic ZnO, AgNO3 and bulk (micron sized) TiO2 added (ionic metal-treated) or ZnO, Ag and TiO2 ENMs added (ENM-treated). A sandy-loam soil was amended with the treated sewage sludge and aged in outdoor lysimeters for six months. Earthworms were exposed to the aged mixtures and a dilution of the mixtures (using control soil–sludge mix). Separate earthworm exposures to as-synthesized ENM and ionic metals salts (Zn/Ag singly) were carried out in the same soil. Earthworm reproduction was depressed by 90% in the high-metal ENM treatment and by 22–27% in the ionic metal and low-metal ENM soil–sludge treatments. Based on total metal concentrations in the soil–sludges the as-synthesised metal salt and ENM exposures predicted Zn was driving observed toxicity in the soil–sludge more than Ag. Earthworms from the high-metal ENM treatment accumulated significantly more Ag than other treatments whereas total Zn concentrations in the earthworms were within the range for earthworm Zn regulation for all treatments. This study suggests that current Zn limits set to provide protection against ionic metal forms may not protect soil biota where metals are input to WWTP in the ENM form

    Impact of pedospheric and atmospheric sulphur nutrition on sulphur metabolism of Allium cepa L., a species with a potential sink capacity for secondary sulphur compounds

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    Onion (Afflum cepa L.) was able to use atmospheric H2S as sole sulphur source for growth. The foliarly absorbed H2S was rapidly metabolized into water-soluble, non-protein thiol compounds, including cysteine, and subsequently into other sulphur compounds in the shoots. In H2S-exposed plants, the accumulation of sulphur compounds in the shoots was nearly linear with the concentration (0.15-0.6 mul l(-1)) and duration of the exposure. Exposure of onion to H2S for up to 1 week did not affect the sulphur content of the roots. Secondary sulphur compounds formed a sink for the foliarly absorbed sulphide, and the sulphur accumulation upon H2S exposure could, for a great part, be ascribed to enhancement of the content of gamma-glutamyl peptides and/or alliins. Furthermore, there was a substantial increase in the sulphate content in the shoots upon H2S exposure. The accumulation of sulphate originated both from the pedosphere and from the oxidation of absorbed atmospheric sulphide, and/or from the degradation of accumulated secondary sulphur compounds. From studies on the interaction between atmospheric and pedospheric sulphur nutrition it was evident that H2S exposure did not result in a down-regulation of the sulphate uptake by the roots
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