Interaction of planting system with radiation-use efficiency in wheat lines.

Radiation-use efficiency (RUE) is an important trait for raising biomass and yield potential in plant breeding. However, the effect of the planting system (PS) on genetic variation in RUE has not been previously investigated. Our objectives were to quantify genetic variation in RUE, biomass and grain yield in raised-bed and flat-basin planting systems, and associations with canopy-architecture traits (flag-leaf angle and curvature). Twelve spring wheat (Triticum aestivum L.) cultivars were evaluated under irrigated conditions for 3 years in North West Mexico using raised-bed and flat-basin planting systems. Canopy architecture traits were measured at booting and anthesis + 7 days. Grain yield (10.6%), biomass (7.6%), and pre-grain-filling RUE (9.7%) were higher in raised beds than flat basins, while a significant planting system × genotype interaction was found for grain yield. Genetic variation in pre-grain-filling RUE was associated with biomass and grain yield in beds and basins. In flat basins, higher pre-grain-filling RUE was correlated with a more upright flag-leaf angle but not in raised beds. In raised beds, cultivars with less upright flag-leaf angle had greater fractional light interception pre-anthesis. Taller semi-dwarf cultivars intercepted relatively more radiation in the beds than the flats before anthesis, consistent with the taller cultivars showing relatively greater increases in yield in beds compared to flats. Our results indicated that the evaluation of genotypes for RUE and biomass in wheat breeding should take into account planting systems to capture genotype × PS effects. In addition, the results demonstrate how flag-leaf angle has a different effect depending on the planting system.

Novel sources of variation in grain Zinc (Zn) concentration in bread wheat germplasm derived from Watkins landraces.

A diverse panel of 245 wheat genotypes, derived from crosses between landraces from the Watkins collection representing global diversity in the early 20th century and the modern wheat cultivar Paragon, was grown at two field sites in the UK in 2015-16 and the concentrations of zinc and iron determined in wholegrain using inductively coupled plasma-mass spectrometry (ICP-MS). Zinc concentrations in wholegrain varied from 24-49 mg kg-1 and were correlated with iron concentration (r = 0.64) and grain protein content (r = 0.14). However, the correlation with yield was low (r = -0.16) indicating little yield dilution. A sub-set of 24 wheat lines were selected from 245 wheat genotypes and characterised for Zn and Fe concentrations in wholegrain and white flour over two sites and years. White flours from 24 selected lines contained 8-15 mg kg-1 of zinc, which was positively correlated with the wholegrain Zn concentration (r = 0.79, averaged across sites and years). This demonstrates the potential to exploit the diversity in landraces to increase the concentration of Zn in wholegrain and flour of modern high yielding bread wheat cultivars.

Gold-coated silica as a preconcentration phase for the determination of total dissolved mercury in natural waters using atomic fluorescence spectrometry.

A novel solid-phase preconcentration method is reported, using in-house gold-coated silica adsorbent packed in a microcolumn, for the determination of dissolved mercury in natural waters by atomic fluorescence spectrometry (AFS). The adsorbent was prepared by chemical reduction of a Au(III) solution with hydroxylamine in the presence of suspended silica particles. The resulting Au nanoparticles on the silica surface were highly efficient for adsorbing different mercury species from acidified waters without additional reagents. The acidified aqueous samples were passed over the microcolumn, either incorporated in a fully automated flow injection (FI) system directly coupled to the AFS or as part of a portable FI system for in situ preconcentration. After rinsing and drying of the column, Hg(0) was released by heating and directed to the AFS cell for quantification. The method offers significant advantages because no reagents are needed for species conversion, preconcentration, sample storage, or desorption and therefore the risk of contamination is minimized and blank values are lowered. This results in a low detection limit of 180 pg L(-1) using a sample volume of only 7 mL and good reproducibility, with relative standard deviations <3.2% (n = 10, [Hg] = 5 ng L(-1)). Recoveries were all >90% in spiked river waters (spiked [Hg] = 0, 1, 5, 10 ng L(-1)), and the experimental value for the certified reference material ORMS-4 (elevated mercury in river water) was 22.3 +/- 2.6 ng Hg L(-1) which was in good agreement with the certified value of 22.0 +/- 1.6 ng Hg L(-1) (recovery = 101%). The method was successfully applied to seven different natural waters and wastewaters ([Hg] 0.5-4.6 ng L(-1)) from south west England.

Protective effects of selenium on mercury-induced DNA damage in mussel haemocytes.

Little is known of the antioxidant role of selenium (Se) in aquatic invertebrates. We investigated the effects of Se on mercury-induced DNA damage in haemocytes from Mytilus edulis using alkaline single cell gel electrophoresis, that is, the Comet assay. The basal percentage tail DNA value for mussel haemocytes was 9.8+/-0.2% (mean+/-S.E.M., n=70). Exposing mussels to Hg(2+) (nominal concentration 20 microgL(-1)) for three days led to an increase in tail DNA to 61.1+/-1.8% (n=10). With added Se (as selenite, nominal concentration 4 microgL(-1)), Hg-induced DNA damage was reduced to 39.5+/-3.1% (n=10). Se pre-exposure also provided some protection against Hg-induced DNA damage (% tail DNA=51.0+/-2.9%, n=10). Basal glutathione peroxidase (GPx) activity in cell-free haemolymph was 93.7+/-3.5 nmol min(-1)mg(-1) (mean+/-S.E.M., n=70). Increases in GPx activity were seen when Se was added during and/or after exposure to Hg. For example, a 3-4-fold increase was seen after three days exposure to Hg in the presence of added Se. Interestingly GPx activity doubled after three days in the presence of added Se alone, but was unchanged after exposure to HgCl(2) alone. These results suggest that the availability of Se in the natural environment could affect the antioxidant status of mussels, and consequently could affect levels of DNA damage.

Bioaccessibility of U, Th and Pb in solid wastes and soils from an abandoned uranium mine.

Bioaccessible U, Th, Pb and the 238U decay products 214Pb and 210Pb have been determined, using a modified Unified BARGE Method (UBM), in waste solids and soils from an abandoned uranium mine in South West England, UK. Maximum aqua regia extractable concentrations for U, Th and Pb were 16,200, 3.8 and 4750 µg g-1, respectively. 238U had highest activity concentrations near the mine shaft, where the decay products214Pb and 210Pb had values of 235 and 180 Bq g-1, respectively. UBM extractions gave mean gastro-intestinal bioaccessibility factors (BAFs) for U and Pb in the waste solids of 0.05 and 0.03, respectively, whereas those for the soils were significantly higher at 0.24 and 0.17. The mean BAFs for the transient radionuclides, 214Pb and 210Pb, were similar to those for stable Pb implying that the stable and radioactive Pb isotopes were attached to similar sites on the particles. The doses arising from the ingestion of particulate 210Pb due to soil pica behaviour were in the range 0.2-65 and < 0.1-6.2 µSv day-1 for a 1-year old child or an adult (>17 years), respectively. The results suggest that the health risk posed by abandoned uranium mines, with waste rock and tailings, throughout the world should take account of the dose due to both bioaccessible radionuclides, as well as their stable counterparts.

Experimental and Computational Modeling of H-Bonded Arginine-Tyrosine Groupings in Aprotic Environments.

H-bonds between neutral tyrosine and arginine in nonpolar environments are modeled by small-molecule phenol/guanidine complexes. From the temperature and concentration dependence of UV spectra, a value of ΔH° = -74 ± 4 kJ mol-1 is deduced for the formation of H-bonded p-cresol/dodecylguanidine in hexane. ΔE = -71 kJ mol-1 is computed with density functional theory (in vacuo). In dimethyl sulfoxide or crystals, (p-phenolyl)alkylguanidines form head-to-tail homodimers with two strong H-bonding interactions, as evidenced by UV, IR, and NMR spectral shifts, strong IR continuum absorbance bands, and short O···N distances in X-ray crystal structures. Phenol/alkylguanidine H-bonded complexes consist of polarizable rapidly interconverting tautomers, with the proton shift from phenol to guanidine increasing with increase in the polarity of the aprotic solvent. As measured by NMR, both groups in these strongly H-bonded neutral complexes can simultaneously appear to be predominantly protonated. These systems serve as models for the hypothetical hydrogen-Bonded Uncharged (aRginine + tYrosine), or "BU(RY)", motifs in membrane proteins.

Methods for the determination and speciation of mercury in natural waters--a review.

This review summarises current knowledge on Hg species and their distribution in the hydrosphere and gives typical concentration ranges in open ocean, coastal and estuarine waters, as well as in rivers, lakes, rain and ground waters. The importance of reliable methods for the determination of Hg species in natural waters and the analytical challenges associated with them are discussed. Approaches for sample collection and storage, pre-concentration, separation, and detection are critically compared. The review covers well established methods for total mercury determination and identifies new approaches that offer advantages such as ease of use and reduced risk of contamination. Pre-concentration and separation techniques for Hg speciation are divided into chromatographic and non-chromatographic methods. Derivatisation methods and the coupling of pre-concentration and/or separation methods to suitable detection techniques are also discussed. Techniques for sample pre-treatment, pre-concentration, separation, and quantification of Hg species, together with examples of total Hg determination and Hg speciation analysis in different natural (non-spiked) waters are summarised in tables, with a focus on applications from the last decade.