Solar flare activity: Evidence for large-scale changes in the past

An analysis of radar and photographic meteor data and of spacecraft meteoroid penetration data indicates that there probably has not been a large increase in meteoroid impact rates in the last 10⁴ yr. The solar flare tracks observed in the glass linings of meteoroid impact pits on lunar rock 15205 are therefore reanalyzed assuming a meteoroid flux that is constant in time. Based on this assumption, the data suggest that the production rate of Fe-group solar flare tracks may have varied by as much as a factor of 50 on a time scale of about 10⁴ yr. No independently obtained data are known to require conflict with this interpretation. Confidence in this conclusion is somewhat qualified by the experimental and analytical uncertainties involved, but the conclusion nevertheless remains the present “best” explanation for the observed data trends.     

Testing Nano-Powder and Fused-Glass Mineral Reference Materials for In Situ Rb-Sr Dating of Glauconite,Phlogopite, Biotite and Feldspar via LA-ICP-MS/MS

Reference materials (RMs) with well-characterised composition are necessary for reliable quantification and quality control of isotopic analyses of geological samples. For in situ Rb-Sr analysis of silicate minerals via laser ablation inductively coupled plasma tandem mass spectrometry (LA-ICP-MS/MS) with a collision/reaction cell, there is a general lack of mineral-specific and matrix-matched RMs, which limits wider application of this new laser-based dating technique to certain minerals. In this work, pressed nano-powder pellets (NP) of four RMs, GL-O (glauconite), Mica-Mg (phlogopite), Mica-Fe (biotite) and FK-N (K-feldspar), were analysed and tested for in situ Rb-Sr dating, complemented by isotope dilution (ID) MC-ICP-MS Rb-Sr analyses of GL-O and Mica-Mg. In addition, we attempted to develop alternative flux-free and fused ‘mineral glasses’ from the above RMs for in situ Rb-Sr dating applications. Overall, the results of this study showed that among the above RMs only two NP (Mica-Mg-NP and GL-O-NP) were suitable and robust for in situ dating applications. These two nano-powder reference materials, Mica-Mg-NP and GL-O-NP, were thus used as primary RMs to normalise and determine Rb-Sr ages for three natural minerals: MDC phlogopite and GL-O glauconite grains, and also Mica-Fe-NP (biotite). Our in situ analyses of the above RMs yielded Rb-Sr ages that are in good agreement (within 8%) of published ages, which suggests that both Mica-Mg-NP and GL-O-NP are suitable RMs for in situ Rb-Sr dating of phlogopite, glauconite and biotite. However, using secondary RMs is recommended to monitor the quality of the obtained ages.     

Physical limits on iron uptake mediated by siderophores or surface reductases

The excretion of siderophores and the reduction of organic iron-complexes at the cell surface are common reactions of terrestrial plants, fungi and bacteria in response to low availability of iron. However, there is much less evidence for the use of these strategies by marine phytoplankton. It has been argued that siderophore excretion is inefficient in an aquatic environment due to rapid diffusion. This study examines how diffusion and chemical reactions in the microenvironment of a phytoplankton cell influence the efficiency of both strategies to increase the bioavailability of iron and to reduce iron stress. A numerical model of the cell surroundings is presented that calculates the concentration distribution for different iron species and allows to study the effect of siderophores or surface reductases. It calculates the efficiency of these mechanisms, defined as the quotient between the increase in iron uptake rate and the excretion rate of siderophores or electrons, needed to obtain this increase. The dependence of this efficiency on rates of iron coordination reactions, on diffusivity, and on the kinetics of iron uptake is discussed with the aid of some analytical calculations.     

Removal of heavy metals from mine water by carbonate precipitation in the Grootfontein-Omatako canal, Namibia

Water from the Kombat mine was delivered to the Omatako dam via the 263-km-long Grootfontein-Omatako canal during test runs in 1997. It is intended to supply water from Kombat and other underground mines in the Otavi Mountain Land to the capital Windhoek. The Cu-Pb-Zn orebodies are hosted by carbonate rocks and the mine waters are supersaturated with respect to calcite and CO₂. Along the length of the canal, the CO₂ partial pressure drops from 10^−2.1 atm at the inlet of the Kombat mine to 10^−3.5 atm at the end of the canal. This is accompanied by a drop in Ca concentration from about 60 to about 20 mg/l. The heavy metal concentrations (Cd, Cu, Mn, Pb and Zn) drop along the course of the canal to values far below the national drinking-water standard. Scavenging by calcium carbonate precipitation is the major depletion mechanism. Received: 21 June 1999 · Accepted: 29 August 1999     

How the performance of hydrological models relates to credibility of projections under climate change

Two approaches can be distinguished in studies of climate change impacts on water resources when accounting for issues related to impact model performance: (1) using a multi-model ensemble disregarding model performance, and (2) using models after their evaluation and considering model performance. We discuss the implications of both approaches in terms of credibility of simulated hydrological indicators for climate change adaptation. For that, we discuss and confirm the hypothesis that a good performance of hydrological models in the historical period increases confidence in projected impacts under climate change, and decreases uncertainty of projections related to hydrological models. Based on this, we find the second approach more trustworthy and recommend using it for impact assessment, especially if results are intended to support adaptation strategies. Guidelines for evaluation of global- and basin-scale models in the historical period, as well as criteria for model rejection from an ensemble as an outlier, are also suggested.     

Characterization of wood-laden flows in rivers

Inorganic sediment is not the only solid-fraction component of river flows; flows may also carry significant amounts of large organic material (i.e. large wood), but the characteristics of these wood-laden flows (WLFs) are not well understood yet. With the aim to shed light on these relatively unexamined phenomena, we collected home videos showing natural flows with wood as the main solid component. Analyses of these videos as well as the watersheds and streams where the videos were recorded allowed us to define for the first time WLFs, describe the main characteristics of these flows and broaden the definition of wood transport regimes (adding a new regime called here hypercongested wood transport). According to our results, WLFs may occur repeatedly, in a large range of catchment sizes, generally in steep, highly confined single thread channels in mountain areas. WLFs are typically highly unsteady and the log motion is non-uniform, as described for other inorganic sediment-laden flows (e.g. debris flows). The conceptual integration of wood into our understanding of flow phenomena is illustrated by a novel classification defining the transition from clear water to hypercongested, wood and sediment-laden flows, according to the composition of the mixture (sediment, wood, and water). We define the relevant metrics for the quantification and modelling of WLFs, including an exhaustive discussion of different modelling approaches (i.e. Voellmy, Bingham and Manning) and provide a first attempt to simulate WLFs. We draw attention to WLF phenomena to encourage further field, theoretical, and experimental investigations that may contribute to a better understanding of flows in river basins, leading to more accurate predictions, and better hazard mitigation and management strategies. © 2019 John Wiley & Sons, Ltd.     

Origins of meteoritic nanodiamonds investigated by coordinated atom‐probe tomography and transmission electron microscopy studies

To constrain the origins of meteoritic nanodiamonds, the abundance ratios of stable C isotopes in acid residues from the carbonaceous chondritic meteorite Allende CV3 were measured using coordinated atom‐probe tomography (APT) and transmission electron microscopy (TEM). We combined our data with previously published APT data. A statistical analysis of this combined data set suggests an upper bound of 1 in 10² on the subpopulation that could have a large isotopic enrichment in ¹³C relative to ¹²C, consistent with the possible detection by secondary ion mass spectrometry of a similar enrichment in a 1 in 10⁵ fraction, abundant enough to account for the Xe‐HL anomalous isotopic component carried by the acid residues. Supernovae are believed to be the source of Xe‐HL, leading to the mystery of why all other supernova minerals do not carry Xe‐HL. The lack of Xe‐HL in low‐density disordered supernova graphite suggests that the isotopically anomalous component is the nanodiamonds, but the disordered C in the residue is not ruled out. We discuss possible origins of the disordered C and implications of our results for proposed formation scenarios for nanodiamonds. At least 99% of the meteoritic acid residue exhibits no unambiguous evidence of presolar formation, although production with solar isotope ratios in asymptotic giant branch stars is not ruled out. Comparison of TEM and APT results indicates that a minority of the APT reconstructions may preferentially sample disordered C rather than nanodiamonds. If this is the case, a presolar origin for a larger fraction of the nanodiamonds remains possible.     

Small-scale transport of trace elements Nb and Cr during growth of titanite: an experimental study at 600?°C, 0.4 GPa

Trace element distribution in titanite overgrowths on rutile has been investigated experimentally at 600?°C, 400?MPa and f_O2 near NiNiO buffer. Compositionally homogenous Cr- or Nb-doped synthetic rutile single crystals or Nb-containing natural rutile crystals were the source of Cr, Nb and Ti to synthesize titanite using the double-capsule technique. All element exchange with the source of Si, Ca and Al occurred via a NaCl–H₂O fluid. Titanite forms quickly and exclusively around the rutile crystals. The titanite overgrowth separates rutile from the bulk fluid, and all elements from rutile dissolution have to pass through the titanite rim. Trace element concentrations in titanite show a considerable scatter in experiments with and without Al, although the average concentrations of Cr or Nb of titanite around compositionally homogeneous synthetic rutile approach the expected values for closed system conditions. Variability of Al with Cr or Nb in the titanite is not correlated. The Al zoning is irregular and patchy, and also the distribution of trace elements does not show systematic trends in the spatial distribution. In experiments using zoned natural rutile, the concentrations of Nb in titanite are related to the Nb zoning in rutile, but the contents also vary unsystematically. Under the controlled conditions of the experiment, the explanation for the strongly irregular spatial distribution is most likely due to variations in elemental concentrations during transport from the rutile along the titanite grain boundaries. The transport pathway is complex because grain boundary migration is important during titanite growth. Such irregular element distribution is also found in a natural sample of titanite overgrowth on rutile from an eclogite with retrograde overprint in the amphibolite facies. Transport of Ti and trace elements was focused on grain boundaries and shielded from the rutile as a source of these elements. We conclude that this type of zoning is not related to changes in P–T or composition in an open system, but solely controlled by transport in and through the titanite rim.