Beat Aeschlimann

Rice endosperm iron biofortification by targeted and synergistic action of nicotianamine synthase and ferritin.

Nearly one-third of the worlds population, mostly women and children, suffer from iron malnutrition and its consequences, such as anaemia or impaired mental development. Iron fortification of food is difficult because soluble iron is either unstable or unpalatable, and non-soluble iron is not bioavailable. Genetic engineering of crop plants to increase iron content has therefore emerged as an alternative for iron biofortification. To date, strategies to increase iron content have relied on single genes, with limited success. Our work focuses on rice as a model plant, because it feeds one-half of the worlds population, including the majority of the iron-malnourished population. Using the targeted expression of two transgenes, nicotianamine synthase and ferritin, we increased the iron content of rice endosperm by more than six-fold. Analysis of transgenic rice lines confirmed that, in combination, they provide a synergistic effect on iron uptake and storage. Laser ablation-inductively coupled plasma-mass spectrometry showed that the iron in the endosperm of the transgenic rice lines accumulated in spots, most probably as a consequence of spatially restricted ferritin accumulation. Agronomic evaluation of the high-iron rice lines did not reveal a yield penalty or significant changes in trait characters, except for a tendency to earlier flowering. Overall, we have demonstrated that rice can be engineered with a small number of genes to achieve iron biofortification at a dietary significant level.

Gold adsorption on the carbon surface of C/Co nanoparticles allows magnetic extraction from extremely diluted aqueous solutions

The elusive chemistry of gold has made refining from ores a difficult task and often involves handling of large volumes of water at low pH values with associated high environmental burden. As a result, the broader use of gold in environmental catalysis, organic synthesis and in electronics is still limited in spite of its most attractive chemistry. Present gold extraction suffers from metal loss in the form of gold adsorbed on active carbon particles that are washed out of the extraction process. Here, we investigate the use of magnetic carbon in the form of carbon-coated metal nanomagnets for ionic gold recovery. In contrast to acid-labile iron oxide nanoparticles, the carbon/cobalt nanomagnets resisted dissolution in acidic refining/recycling waters. Repetitive extraction runs demonstrated the possibility to recycle the magnetic reagent. A series of dilution studies showed a high affinity of the ionic gold to the carbon surfaces of the nanomagnets which enabled gold extraction down to the part per billion level (microgram per litre). Detailed investigations on the morphology of the Au-loaded nanomagnets after use suggest a mechanism based on the selective reduction of ionic gold on the C/Co surface and transfer of cobalt through the carbon shell. The resulting irreversible deposition of metallic gold correlated with the release of oxidized (ionic) cobalt into the aqueous phase.

Quantitative Chemical Imaging of Element Diffusion into Heterogeneous Media Using Laser Ablation Inductively Coupled Plasma Mass Spectrometry, Synchrotron Micro-X-ray Fluorescence, and Extended X-ray Absorption Fine Structure Spectroscopy

Quantitative chemical imaging of trace elements in heterogeneous media is important for the fundamental understanding of a broad range of chemical and physical processes. The primary aim of this study was to develop an analytical methodology for quantitative high spatial resolution chemical imaging based on the complementary use of independent microanalytical techniques. The selected scientific case study is focused on high spatially resolved quantitative imaging of major elements, minor elements, and a trace element (Cs) in Opalinus clay, which has been proposed as the host rock for high-level radioactive waste repositories. Laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS), providing quantitative chemical information, and synchrotron radiation based micro-X-ray fluorescence (SR-microXRF), providing high spatial resolution images, were applied to study Cs migration into Opalinus clay rock. The results indicate that combining the outputs achievable by the two independent techniques enhances the imaging capabilities significantly. The qualitative high resolution image of SR-microXRF is in good agreement with the quantitative image recorded with lower spatial resolution by LA-ICPMS. Combining both techniques, it was possible to determine that the Opalinus clay sample contains two distinct domains: (i) a clay mineral rich domain and (ii) a calcium carbonate dominated domain. The two domains are separated by sharp boundaries. The spatial Cs distribution is highly correlated to the distribution of the clay. Furthermore, extended X-ray absorption fine structure analysis indicates that the trace element Cs preferentially migrates into clay interlayers rather than into the calcite domain, which complements the results acquired by LA-ICPMS and SR-microXRF. By using complementary techniques, the quantification robustness was improved to quantitative micrometer spatial resolution. Such quantitative, microscale chemical images allow a more detailed understanding of the chemical reactive transport process into and within heterogeneous media to be gained.

Climate-controlled multidecadal variability in North African dust transport to the Mediterranean

High-resolution laser ablation–inductively coupled plasma–mass spectroscopy scanning of resin-embedded laminated sediments is used to detail variability in the composition and magnitude of recent eolian dust deposition in the Eastern Mediterranean. The composition of dust accumulating in the anoxic Atalante basin varies in response to the strength of the summer blocking mode of Mediterranean climate. Dust sources located upwind on the westerly airflow are favored during phases of weaker blocking (hence stronger summer westerlies). This mode is in turn correlated to the pronounced multidecadal oscillation in Mediterranean sea-surface temperature (related to the Atlantic Multidecadal Oscillation), suggesting that coupled ocean-atmosphere dynamics control the large-scale transport of dust in the region. Variable precipitation in dust source regions may also exert an influence on the relative flux of dust from each source, and hence the net composition of dust deposited in the basin. Persistent oscillations in the composition of deeper sediments indicate that the basin offers a high-potential archive for reconstruction of climate-controlled variability in dust transport prior to the instrumental era.

Development and characterization of custom-engineered and compacted nanoparticles as calibration materials for quantification using LA-ICP-MS

The flame spray technique was used to produce a nano-material with a customized composition. Liquid organic precursors of Si, Ca, Ti, Mg, Fe, and Al in a concentration similar to the matrix of the well-known NIST SRM 610 glass standard were mixed with a selection of rare earth elements (Ce, Gd, Ho, and Tb), precious metals (Ag, Au, Pd, Pt, Rh, and Ru) and Pb at concentrations of approx. 400–500 mg kg−1. The liquid precursor mixture was sprayed and collected as nanopowder, compacted to pellets and analyzed by solution and laser-ablation inductively coupled plasma mass spectrometry. The bulk composition of the material was determined in several aliquots of the powder, either 25 mg or 50 mg. Electron microprobe analyses were carried out to further characterize the major element composition of the pressed nano-material. The pellet was ablated using different laser ablation systems with an aim of assessing the micro-scale homogeneity of the produced material. The manufactured material is homogeneous for major elements and REEs similar to the NIST glass (<5% RSD). However, the distribution of the PGEs showed some larger spatial variation in the order of <7.5%. In addition it is shown that contamination during production leads to heterogeneous distribution of Pb and Ag. Based on the results achieved for Ru, Rh, Pd, Au, Pt, Mg, Ti, and Fe, which are either absent or not available in sufficient concentration levels in NIST glass, it is demonstrated that flame spray synthesis allows production of suitable customized matrix-matched calibration materials for micro-analytical techniques.

High spatial resolution quantitative imaging by cross-calibration using Laser Ablation Inductively Coupled Plasma Mass Spectrometry and Synchrotron micro-X-ray Fluorescence technique.

High spatial resolution, quantitative chemical imaging is of importance to various scientific communities, however high spatial resolution and robust quantification are not trivial to attain at the same time. In order to achieve microscopic chemical imaging with enhanced quantification capabilities, the current study links the independent and complementary advantages of two micro-analytical techniques - Synchrotron Radiation-based micro X-ray Fluorescence (SR-microXRF) and Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICPMS). A cross-calibration approach is established between these two techniques and validated by one experimental demonstration. In the presented test case, the diffusion pattern of trace level Cs migrating into a heterogeneous geological medium is imaged quantitatively with high spatial resolution. The one-dimensional line scans and the two-dimensional chemical images reveal two distinct types of geochemical domains: calcium carbonate rich domains and clay rich domains. During the diffusion, Cs shows a much higher interfacial reactivity within the clay rich domain, and turns out to be nearly non-reactive in the calcium carbonate domains. Such information obtained on the micrometer scale improves our chemical knowledge concerning reactive solute transport mechanism in heterogeneous media. Related to the chosen demonstration study, the outcome of the quantitative, microscopic chemical imaging contributes to a refined safety assessment of potential host rock materials for deep-geological nuclear waste storage repositories.