RESUMEN
The stability of organic matter-iron-phosphate (OM-Fe-P) association has an important impact on the migration and sequestration of organic carbon (OC) and P in the environment. Here, we examined the release characteristics of Fe, P and OM due to the abiotic reduction of OM-Fe-P associations by Na-dithionite. The associations were synthesized with algae-derived OM (AOM) and terrestrial humic acid (HA) through either adsorption onto iron (hydr)oxide or coprecipitation with Fe(III). Results indicated that OM and P adsorbed onto the associations were rapidly released, whereas coprecipitation yielded much lower release rates of Fe, P, and OM. The stronger inhibitory effect on reduction from coprecipitation can be explained by larger particles formed by coprecipitation and coprecipitation taking up more OC that had a passivation effect on the associations. The release rates of OM and P were lower in coprecipitates formed with HA than formed with AOM for a given OC/Fe ratio. This observation can be attributed to a patchy distribution of OC in AOM associated coprecipitates, which showed a weaker aggregation of OC with Fe and P. In contrast, the distribution of OC in HA-associated coprecipitates was more homogenous, enabling a stronger aggregation of OM with P and a greater passivation effect on P release. Our results revealed that OM sources, association formation pathways, and elemental stoichiometry collectively controlled the stability of OM-Fe-P associations.
RESUMEN
Smectite clays are widely found in subsurface soils and waters. Although they strongly sequester tetracyclines (TCs), little is known about their reactions with these antibiotics under dark anoxic conditions. This study investigated the interactions between TCs and Fe-bearing smectite clays and the influences of environmental factors. Fe-bearing smectite clays were shown to significantly induce the transformation of TCs, including tautomerization, dechlorination, and dehydration. Moreover, the adsorbed TCs reduced the structural Fe(III) in clay particles to structural Fe(II) through electron transfer. The transformation of TCs was more readily induced by smectite clays with a higher rather than a lower Fe content. Tetrahedral Fe(III), and distorted cis- or trans-octahedral Fe(III), were more reactive as an electron acceptor than cis-octahedral Fe(III), as observed on the Mössbauer and FTIR spectra. A lower pH facilitated the adsorption of TCs through dimethyl-amino, amide, and conjugated -OH functional groups and induced a higher rate of TCs transformation. The transformation of chlortetracycline (CTC) was faster than that of oxytetracycline or tetracycline (TTC) due to -Cl substitution. The major transformation CTC products included keto-CTC, epi-CTC, iso-CTC, anhydro-CTC and TTC. Mixtures of these transformed products were found to have a higher acute toxicity than their parent compounds to Photobacterium phosphoreum T3. Our study revealed several previously overlooked interactions between TCs and clay particles that could cause these antibiotics to become unstable in the subsurface environment, with negative effects on the soil-borne microbial community.
Asunto(s)
Arcilla , Tetraciclinas , Antibacterianos , Compuestos Férricos , SilicatosRESUMEN
Three experiments are reviewed, performed (in 2014-2016) at ID18 of ESRF to measure the influence of acceleration on time dilation by measuring the relative shift between the absorption lines of two states of the same rotating absorber with accelerations anti-parallel and parallel to the incident beam. Statistically significant data for rotation frequencies up to 510â Hz in both directions of rotation were collected. For each run with high rotation, a stable statistically significant `vibration-free' relative shift between the absorption lines of the two states was measured. This may indicate the influence of acceleration on time dilation. However, the measured relative shift was also affected by the use of a slit necessary to focus the beam to the axis of rotation to a focal spot of sub-micrometre size. The introduction of the slit broke the symmetry in the absorption lines due to the nuclear lighthouse effect and affected the measured relative shift, preventing to claim conclusively the influence of acceleration on time dilation. Assuming that this loss of symmetry is of first order, the zero value of the relative shift, corrected for this loss, falls always within the experimental error limits, as predicted by Einstein's clock hypothesis. The requirements and an indispensable plan for a conclusive experiment, once the improved technology becomes available, is presented. This will be useful to future experimentalists wishing to pursue this experiment or a related rotor experiment involving a Mössbauer absorber and a synchrotron Mössbauer source.
RESUMEN
New results, additional techniques and know-how acquired, developed and employed in a recent HC-1898 experiment at the Nuclear Resonance Beamline ID18 of ESRF are presented, in the quest to explore the acceleration effect on time dilation. Using the specially modified Synchrotron Mössbauer Source and KB-optics together with a rotating single-line semicircular Mössbauer absorber on the rim of a specially designed rotating disk, the aim was to measure the relative spectral shift between the spectra of two states when the acceleration of the absorber is anti-parallel and parallel to the source. A control system was used for the first time and a method to quantify the effects of non-random vibrations on the spectral shift was developed. For several runs where the effect of these vibrations was negligible, a stable statistically significant non-zero relative shift was observed. This suggests the influence of acceleration on time.