Redox-active iron minerals can act as energy sources or electron-transferring mediators in microbial syntrophic associations, being important means of interspecies metabolic cooperation in sedimentary environments. Alkaline conditions alter the thermodynamic stability of iron minerals, influencing their availability for interspecies syntrophic interactions. We have modeled anaerobic alkaliphilic microbial associations in ethanol-oxidizing co-culture of an obligate syntroph Candidatus “Contubernalis alkalaceticum” and a facultative lithotroph Geoalkalibacter ferrihydriticus, which is capable of dissimilatory Fe(III) reduction and homoacetogenic oxidation of Fe(II) with CO₂. The co-cultures were cultivated with thermodynamically metastable ferric-containing ferrihydrite, or ferrous-containing siderite, or without minerals. Mössbauer spectral analysis revealed the transformation of both minerals to the stable magnetite. In the presence of ferrihydrite, G. ferrihydriticus firstly reduced Fe(III) with ethanol and then switched to syntrophic homoacetogenesis, providing the growth of obligate syntroph on ethanol. The ability of G. ferrihydriticus to accept hydrogen from its syntrophic partner and produce extra acetate from carbonate during ethanol oxidation was confirmed by co-culture growth without minerals. In the presence of siderite, G. ferrihydriticus performed homoacetogenesis using two electron donors simultaneously— siderite and hydrogen. Pieces of evidence for direct and indirect hydrogen-mediated electron exchange between partner organisms were obtained. Relative abundancies of partner organisms and the rate of acetate production by their co-cultures were strongly determined by thermodynamic benefits, which G. ferrihydriticus got from redox transformations of iron minerals. Even the minor growth of G. ferrihydriticus sustained the growth of the syntroph. Accordingly, microbe-to-mineral interactions could represent underestimated drivers of syntrophic interactions in alkaline sedimentary environments.

The multilayer of approximate structure MgO(100)/[ⁿFe₅₁Rh₄₉(63 Å)/⁵⁷Fe₅₁Rh₄₉(46 Å)]₁₀ deposited at 200 °C is primarily of paramagnetic A1 phase and is fully converted to the magnetic B2 phase by annealing at 300 °C for 60 min. Subsequent irradiation by 120 keV Ne⁺ ions turns the thin film completely to the paramagnetic A1 phase. Repeated annealing at 300 °C for 60 min results in 100% magnetic B2 phase, i.e. a process that appears to be reversible at least twice. The A1 → B2 transformation takes place without any plane-perpendicular diffusion while Ne⁺ irradiation results in significant interlayer mixing.

Iron (Fe) is an essential cofactor for all livings. Although Fe membrane transport mechanisms often utilize Fe^II, uncoordinated or deliberated ferrous ions can initiate Fenton reactions. Fe^III citrate complexes are among the most important complexed forms of Fe^III especially in plants that, indeed, can undergo photoreduction. Since leaves as photosynthetic organs of higher plants are generally exposed to illumination in daytime, photoreaction of ferric species may have biological relevance in iron metabolism, the relevance of which is poorly understood. In present work Fe^III citrate transformation during the photodegradation in solution and after foliar application on leaves was studied by Mössbauer analysis directly. To obtain irradiation time dependence of the speciation of iron in solutions, four model solutions of different pH values (1.5, 3.3, 5.5, and 7.0) with Fe to citrate molar ratio 1:1.1 were exposed to light. Highly acidic conditions led to a complete reduction of Fe together with the formation of Fe^II citrate and hexaaqua complexes in equal concentration. At higher pH, the only product of the photodegradation was Fe^II citrate, which was later reoxidized and polymerized, resulting in the formation of polynuclear stable ferric compound. To test biological relevance, leaves of cabbage were treated with Fe^III citrate solution. X-ray fluorescence imaging indicated the accumulation of Fe in the treated leaf parts. Mössbauer analysis revealed the presence of several ferric species incorporated into the biological structure. The Fe speciation observed should be considered in biological systems where Fe^III citrate has a ubiquitous role in Fe acquisition and homeostasis. Graphical abstract

Magnetic nanopatterns were successfully created in FeRh thin film deposited on MgO (100) substrates. Silica and polystyrene spherical masks, nominally 500 and 1000 nm in diameter, respectively were applied on the surface of the sample in order to locally shadow the film against the effect of 110 keV energy neon-ion irradiation with fluences of 10¹⁵ and 10¹⁶ ions/cm². Such nanosphere-lithography technique allows for projecting the mask geometry on the magnetic structure of the FeRh film. Conversion-electron Mössbauer spectroscopy and magnetic force microscopy were used to determine the ferromagnetic ratio and the magnetic pattern in the samples, and nuclear resonance scattering of synchrotron radiation was applied to obtain the in-depth magnetic profile. From the results obtained, the possible three-dimensional (3D) structure of the created individual magnetic domains was also constructed. Overall, the great customizability of the presented nanosphere-lithography technique in FeRh thin film provides opportunities for developing cutting-edge spintronic applications.

Nanotechnology has been evolving in the past decades as an alternative to conventional fertilizers. Ferrihydrite nanoparticles that model the available Fe pool of soils are proposed to be used to recover Fe deficiency of plants. Nevertheless, ferrihydrite aqueous suspensions are known to undergo slow transformation to a mixture of goethite and hematite, which may influence its biological availability. Several nanocolloid suspensions differing in the surfactant type were prepared for plant treatment and fully characterized by transmission electron microscopy and ⁵⁷Fe Mössbauer spectroscopy supported by magnetic measurements. The rate of transformation and the final mineral composition were revealed for all the applied surfactants. Nanomaterials at different stages of transformations were the subject of plant physiological experiments aiming at comparing the behavior and plant accessibility of the manufactured suspensions of nanoscale iron(III) oxide and oxide–hydroxide particles. Graphical abstract

The effect of laser irradiation in the energy range from 20 mW to 200 mW was investigated in 109 nm thick Fe₅₁Rh₄₉ film deposited on an MgO (100) substrate. The initial, A1 structure with fully paramagnetic magnetic ordering was achieved after irradiating the samples with 120 keV Ne⁺ ions with a fluence of 1 × 10¹⁶ ion cm⁻², as it was confirmed by conversion-electron Mössbauer spectroscopy. At higher powers physical damage of the layer was observed, while in the lowest power case, magnetic force microscopy revealed a well-defined magnetic structure reflecting the laser irradiation pattern. The presented results have the potential to be employed for laser ablation or allows the fabrication of arbitrary ferromagnetic pattern within a homogeneous paramagnetic FeRh thin films.