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Lipid ordering in cell membranes has been increasingly recognized as an important factor in establishing and regulating a large variety of biological functions. Multiple investigations into lipid organization focused on assessing ordering from temperature-induced phase transitions, which are often well outside the physiological range. However, particular stresses elicited by environmental factors, such as hypo-osmotic stress or protein insertion into membranes, with respect to changes in lipid status and ordering at constant temperature are insufficiently described. To fill these gaps in our knowledge, we exploited the well-established ability of environmentally sensitive membrane probes to detect intramembrane changes at the molecular level. Our steady state fluorescence spectroscopy experiments focused on assessing changes in optical responses of Laurdan and diphenylhexatriene upon exposure of red blood cells to hypo-osmotic stress and pore-forming toxins at room temperature. We verified our utilized experimental systems by a direct comparison of the results with prior reports on artificial membranes and cholesterol-depleted membranes undergoing temperature changes. The significant changes observed in the lipid order after exposure to hypo-osmotic stress or pore-forming toxins resembled phase transitions of lipids in membranes, which we explained by considering the short-range interactions between membrane components and the hydrophobic mismatch between membrane thickness and inserted proteins. Our results suggest that measurements of optical responses from the membrane probes constitute an appropriate method for assessing the status of lipids and phase transitions in target membranes exposed to mechanical stresses or upon the insertion of transmembrane proteins.

Background: Meeting the global demand for grain is becoming increasingly difficult due to numerous factors including climate variability, urbanization, increasingly frequent extreme weather events and drought. Stalk lodging destroys between 5%-25% of grain crops annually. Developing crop varieties with improved lodging resistance will reduce the frequency and impact of stalk lodging and consequently reduce the yield gap. Field-phenotyping equipment is critical to develop lodging resistant crop varieties, but the effectiveness of current equipment is hindered by measurement error. Relatively little research has been done to identify and rectify sources of measurement error in biomechanical phenotyping platforms. This study specifically investigated sources of error in bending stiffness and bending strength measurements which are often acquired using field-phenotyping devices. Three specific sources of error in bending stiffness and bending strength measurements were evaluated: horizontal device placement, vertical device placement and incorrect recordings of load cell height. Results: Incorrect load cell heights introduced errors as large as 130% in bending stiffness and 50% in bending strength. Results indicated that errors on the order of 15%-25% in bending stiffness and 1–10% in bending strength are common in field-based measurements. Improving operating procedures and protocols can mitigate this error. Such improvements include emphasizing attention to detail while conducting tests and improving the design of phenotyping equipment. Conclusion: Reducing measurement error in field-phenotyping equipment is crucial for advancing the development of improved, lodging-resistant crop varieties. The study found that incorrect load cell height entry and incorrect device placement both significantly contributed to measurement error in bending stiffness and bending strength measurements. These findings have important implications for reducing the yield gap in staple crops and meeting the global demand for grain.

Combustion synthesis in uranyl nitrate-acetylacetone-2-methoxyethanol solutions was used to deposit thin UO2 films on aluminum substrates to investigate the irradiation-induced restructuring processes. Thermal analysis revealed that the combustion reactions in these solutions are initiated at ∼160 °C. The heat released during the process and the subsequent brief annealing at 400 °C allow the deposition of polycrystalline films with 5-10 nm UO2 grains. The use of multiple deposition cycles enables tuning of the film thicknesses in the 35-260 nm range. Irradiation with Ar2+ ions (1.7 MeV energy and a fluence of up to 1 × 1017 ions/cm2) is utilized to generate a uniform distribution of atomic displacements within the films. X-ray fluorescence (XRF) and alpha-particle emission spectroscopy showed that the films were stable under irradiation and did not undergo sputtering degradation. X-ray photoelectron spectroscopy (XPS) showed that the stoichiometry and uranium ionic concentrations remain stable during irradiation. The high-resolution electron microscopy imaging and electron diffraction analysis demonstrated that at the early stages of irradiation (below 1 × 1016 ion/cm2) UO2 films show complete amorphization and beam-induced densification (sintering), resulting in a pore-free disordered film. Prolonged irradiation (5 × 1016 ion/cm2) is shown to trigger a crystallization process at the surface of the films that moves toward the UO2/Al interface, converting the entire amorphous material into a highly crystalline film. This work reports on an entirely different radiation-induced restructuring of the nanoscale UO2 compared to the coarse-grained counterpart. The preparation of thin UO2 films deposited on Al substrates fills an area of national need within the stockpile stewardship program of the National Nuclear Security Administration and fundamental research with actinides. The method reported in this work produces pure, robust, and uniform thin-film actinide targets for nuclear science measurements.

The Structural Maintenance of Chromosomes (SMC) complexes cohesin and condensin establish the 3D organization of mitotic chromosomes1–3. Cohesin is essential to maintain sister chromatid pairing until anaphase onset4, while condensin is important for mitotic centromere structure and elastic resistance to spindle forces5–8. Both complexes are also important to form productive kinetochore-spindle attachments6, 8, 9. How condensin and cohesin work together to shape the mitotic centromere to ensure faithful chromosome segregation remains unclear. Here we show by super-resolution imaging, Capture-C analysis and polymer modeling that vertebrate centromeres are partitioned into two distinct condensin-dependent subdomains during mitosis. This bipartite sub-structure is found in human, mouse and chicken centromeres and also in human neocentromeres devoid of satellite repeats, and is therefore a fundamental feature of vertebrate centromere identity. Super-resolution imaging reveals that bipartite centromeres assemble bipartite kinetochores with each subdomain capable of binding a distinct microtubule bundle. Cohesin helps to link the centromere subdomains, limiting their separation in response to mitotic spindle forces. In its absence, separated bipartite kinetochores frequently engage in merotelic spindle attachments. Consistently, uncoupling of centromere subdomains is a common feature of lagging chromosomes in cancer cells. The two-domain structure of vertebrate regional centromeres described here incorporates architectural roles for both condensin and cohesin and may have implications for avoiding chromosomal instability in cancer cells.

We report on the reversible, electrochemical (de)fluorination of the defect fluoride pyrochlore CsMnFeF6 at room temperature using a liquid electrolyte. CsMnFeF6 was synthesized via three different methods (hydrothermal, ceramic, and mechanochemical), each of which yield products of varying particle size and phase purity. Using galvanostatic cycling, we found that after three oxidative/ reductive cycles, approximately one fluoride ion can be reversibly inserted and removed from mechanochemically synthesized CsMnFeF6 for multiple cycles. Ex-situ X-ray absorption spectroscopy confirmed that both the Mn2+ and Fe3+ in this composition are redox active during cycling. Electrochemical impedance spectroscopy and ex-situ synchrotron powder diffraction were utilized to investigate the delayed onset of significant fluoride (de)insertion. We observed decreased impedance after one full cycle and subtle expansion and contraction of the CsMnFeF6 cubic lattice on oxidation (insertion) and reduction (removal), respectively, over the first two cycles. Our results suggest the formation of fluoride vacancies in early cycles generates mixed-valent Fe that enhances the conductivity and improves the reversibility in later cycles.

Cohesin organizes the genome by forming intra-chromosomal loops and inter-sister chromatid linkages. During gamete formation by meiosis, chromosomes are reshaped to support crossover recombination and two consecutive rounds of chromosome segregation. Here we show that Eco1 acetyltransferase positions both chromatin loops and sister chromatid cohesion to organize meiotic chromosomes into functional domains in budding yeast. Eco1 acetylates the Smc3 cohesin subunit in meiotic S phase to establish chromatin boundaries, independently of DNA replication. Boundary formation by Eco1 is critical for prophase exit and for the maintenance of cohesion until meiosis II, but is independent of the ability of Eco1 to antagonize the cohesin-release factor, Wpl1. Conversely, prevention of cohesin release by Wpl1 is essential for centromeric cohesion, kinetochore monoorientation and co-segregation of sister chromatids in meiosis I. Our findings establish Eco1 as a key determinant of chromatin boundaries and cohesion positioning, revealing how local chromosome structuring directs genome transmission into gametes.

Off-Site Modular Construction (OSMC) research has been a growing research area over the past two decades because of low productivity in construction. Tools are superior in factories and productivity is much higher compared to a stick built site. This has spawned the development small, factory built, rapidly deployable and flexible process plants to take advantage of the gains in OSMC productivity. Chemical process plant research is studying fast, automated design and configuration. In this paper, a literature review was performed on modular factory manufactured process plants. The literature review found that moving to small scale OSMC plant systems could enable cost and schedule savings and months of design time compared to the previous on-site assembly design. It was also found that while automation has been applied in earlier stages of the plant design process, a layout optimisation methodology has not been applied to small OSMC process plants. The paper then proposes to utilise a mathematical layout optimisation model to help design and construct modular process plants and considers how this may fit into the process plant design process, as well as considering the transport requirements for modules.

Combustion synthesis in uranyl nitrate-acetylacetone-2-methoxyethanol solutions was used to deposit thin UO

The Small Modular Reactor (SMR) concept is designed such that it will solve some of the construction problems of large reactors. SMRs are designed to be “shop fabricated and then transported as modules to the sites for installation” (IAEA, 2018). As a consequence they theoretically have shorter build schedules and require less capital investment (Locatelli et al., 2014). Factory built modules can also increase safety and productivity, due to higher quality tools and inspection available. A literature review has highlighted substantial work has been undertaken in the research, development and construction of different types of reactors and reactor modules but the design of balance of plant modules has not been extensively researched (Wrigley et al., 2018). The focus of this paper is a case study for balance of plant modules in a light water reactor which also could have applications to other reactor types. Modules that are designed for factory build and transport may be built in a standardized module approach. By maximizing module size for transport, this maximizes work offsite, to achieve the cost and schedule savings associated. A design method needs to be developed to help support this approach. To enable this, a three step method is proposed: group components into modules, layout the modules and arrange components inside the modules. The Shearon Harris nuclear power plant was chosen for its publically available data. A previous study on this plant used matrix reordering techniques to group components and heuristically assign them to large modules, built for construction in an assembly area on site, highlighting a potential capital cost savings of 15%. This paper utilizes the same allocation of components to modules as the previous study but aims to undertake the challenge of how balance of plant modules should be arranged. The literature review highlighted that although the facility and plant layout problem has been extensively researched, mathematical layout optimization has not been applied to nuclear power plants. Many techniques for layout optimization have been developed for facilities and process plants however. The work in this paper develops an optimization model using a genetic algorithm for module layout and allocation within a nuclear power plant. This paper analysed two configurations of modules, where balance of plant modules are located on either one or two sides of the nuclear island. The objective function was to minimise pipe length. In the original research, where the plant was configured for assembly on site, the balance of plant modules are located around three sides of the nuclear island. The objective function was calculated at 14,914. As the distances are calculated rectilinearly, this number would be higher in reality as pipework has to be routed around containment. The optimization reduced the objective function by 33.9% and 37.8% for the three and four floor layouts respectively when balance of plant modules are located on two sides of the nuclear island. Furthermore, when modules are located on one side of the nuclear island, the objective function was reduced by 45.4% and 46.1% for three and four floor layouts respectively. This will reduce materials used, reduce build time and hence reduce the cost of a nuclear power plant. This method will also save design time when developing the layout of modules around the plant.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells. Chromatin immunoprecipitation (ChIP) is a powerful method for assaying protein–DNA binding in vivo and is broadly used to estimate the density of DNA-bound proteins at specific sites in the genome. ChIP is a multistep assay and every step needs to be optimized for consistent results. Briefly, protein–DNA associations are immobilized by cross-linking with formaldehyde [1,2,3] before shearing the chromatin, either mechanically [4] or by enzymatic digestion [5] into DNA fragments of average size 200–500bp. Specific cross-linked protein–DNA complexes are then isolated by immunoprecipitation using an antibody to the protein of interest. Finally, the cross-links are reversed, and the retrieved DNA is analyzed to determine the sequences bound by the protein. ChIP followed by quantitative real-time PCR (ChIP-qPCR), using specific primers, can be used to measure protein association and relative abundance at a particular genomic locus. Alternatively, ChIP can be combined with next generation sequencing (ChIP-seq) to provide a genome-wide view of protein occupancy. While ChIP-seq allows for relative protein abundance at distinct chromosomal addresses to be compared within a sample, differences between samples cannot be quantified without introducing a method to normalize. Typically, this involves “spike in” of a known amount of DNA or cross-linked cells from a different species, with sufficient sequence divergence from the organism of interest to allow sequencing reads to be confidently distinguished bioinformatically [6,7,8]. This technique, referred to as calibrated ChIP-seq, makes it possible to quantitate genome-wide changes in the distribution of an epitope tagged protein and allows for quantification of differences in occupancy between experimental samples [8]. Calibrated ChIP-seq requires that both calibration and experimental organisms carry the same epitope tag and can be immunoprecipitated by the same protocol. For this protocol we use S. pombe to calibrate S. cerevisiae, a combination that also allows us to invert the roles, that is, calibrate S. pombe with S. cerevisiae. The ChIP method described here has been optimized for use with chromatin from two species of yeast,S. cerevisiae and S. pombe; however, it should be easy to adapt it for use with other chromatin sources. To demonstrate the robustness of our ChIP and library preparation protocols we performed ChIP against the Scc1 subunit of the cohesin multiprotein complex, tagged with the 6HA epitope [9,10,11] . We have also used a similar protocol for the condensin subunit Brn1 [12] and for the meiotic counterpart of cohesin, Rec8 [13]. Here, we outline in detail an optimized protocol for cross-linking and harvesting cells, fragmenting chromatin, immunoprecipitating the desired protein–DNA complexes, and preparing the library for sequencing on the Illumina MiniSeq platform. A schematic stepwise representation of the method is illustrated in Fig.1. References: Solomon MJ, Varshavsky A (1985) Formaldehyde-mediated DNA-protein crosslinking: a probe for in vivo chromatin structures. Proc Natl Acad Sci U S A 82(19):6470–6474 Solomon MJ, Larsen PL, Varshavsky A (1988) Mapping protein-DNA interactions in vivo with formaldehyde: evidence that histone H4 is retained on a highly transcribed gene. Cell 53(6):937–947 Gilmour DS, Lis JT (1984) Detecting protein-DNA interactions in vivo: distribution of RNA polymerase on specific bacterial genes. Proc Natl Acad Sci U S A 81(14):4275–4279 Kuo MH, Allis CD (1999) In vivo cross-linking and immunoprecipitation for studying dynamic protein:DNA associations in a chromatin environment. Methods 19(3):425–433.https://doi.org/10.1006/meth.1999.0879 Thorne AW, Myers FA, Hebbes TR (2004) Native chromatin immunoprecipitation. Methods Mol Biol 287:21–44.https://doi.org/10.1385/1-59259-828-5:021 Bonhoure N, Bounova G, Bernasconi D, Praz V, Lammers F, Canella D, Willis IM, Herr W, Hernandez N, Delorenzi M, Cycli XC (2014) Quantifying ChIP-seq data: a spiking method providing an internal reference for sample-to-sample normalization. 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Nat Methods 5(10):887–893.https://doi.org/10.1038/nmeth.1251 Ford E, Nikopoulou C, Kokkalis A, Thanos D (2014) A method for generating highly multiplexed ChIP-seq libraries. BMC Res Notes 7:312. https://doi.org/10.1186/1756-0500-7-312 Acknowledgements: We are grateful to Manu Shukla for discussions and comments on the ChIP-seq library preparation and for kindly providing a representative Bioanalyzer image, Nicholas Toda, Jesus Torres-Garcia, and Flora Paldi for sharing tips on the ChIP-seq library protocol and Stefan Galangher and Lesley Clayton for general comments on the manuscript. This work was funded by Wellcome through a Senior Research Fellowship to AM and a Wellcome Centre core grant [107827 and 203149].

A plethora of biological processes like gene transcription, DNA replication, DNA recombination, and chromosome segregation are mediated through protein–DNA interactions. A powerful method for investigating proteins within a native chromatin environment in the cell is chromatin immunoprecipitation (ChIP). Combined with the recent technological advancement in next generation sequencing, the ChIP assay can map the exact binding sites of a protein of interest across the entire genome. Here we describe a-step-by step protocol for ChIP followed by library preparation for ChIP-seq from yeast cells.

A heat sink module has been developed for high-heat flux applications in the divertor region of a near term DEMO divertor. The concept employs water jet impingement, in a cascading flow path, together with CuCrZr as the structural material. This fluid-flow architecture maximises the heat transfer coefficient obtained for a given coolant flow rate. Combined with high operational pressures, it facilitates increased coolant outlet temperatures. A conjugate CFD study was performed to compare its performance to the ITER divertor under a representative heat flux boundary condition of 10 MW/m2. A transient thermochromic liquid crystal technique was used to experimentally validate the CFD heat transfer data, using air as the working fluid at matched Reynolds numbers. These results showed that area averaged heat transfer coefficients could be accurately predicted by the CFD to within ∼12%.

The influence of high-energy (1.6 MeV) Ar

Irradiation performance of multilayer HBC foils which layers are more than 20 were conducted for the first time, and different types of carbon stripper foils were dosed under a series of irradiation conditions systematically. Eight (8) types of carbon stripper foils were striked by Ar4+ beam under different intensities and fluences. Multilayer foils performed generally better than the monolayer ones. The existence of boron layer helped to increase the resistance of the foils to irradiation damage, elongating their lifetimes.

Hard chromium plate (HCP) has been the wear resistant coating of choice in the nuclear industry for decades, but new protective coatings are required as a result of the hazardous nature of Cr(VI) compounds used in electroplating. This study compares the wear performance of candidate replacements materials, Cr2O3 and Cr3C2–NiCr. These two coatings are also compared with HCP and a WC-(W,Cr)2C–Ni coating assessed in an earlier publication. The Cr2O3 and Cr3C2–NiCr coatings were supplied having been applied to Inconel 625 substrates using high velocity oxy fuel (HVOF) and thermal detonation gun spray techniques, respectively. A ball-on-flat sliding wear configuration was used with three environments: dry, deionised water, and borated water to partially simulate nuclear reactor water chemistry. Wear rates were measured using both volume and mass standard metrics. The wear surface samples were characterised using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) in order to establish the operative wear mechanisms. All three candidate coating materials exhibited similar wear performance to HCP in the three test environments. There was, however, enough of a difference between performance in deionised and borated water, to merit the use of borated water in future testing. The data gathered using SEM and XPS provided insight into the wear mechanisms. These include both particle pull-out and tribolayer formation. The XPS data revealed that Cr3C2 is preferentially removed from the Cr3C2–NiCr coating during wear testing in a borated water environment.

Charge cycling cross sections of lithium and helium ions are measured for atomic metal films of titanium, zirconium and copper. The material dependence of the measured charge state fractions is investigated and compared with the material density, electron density, mean ionization potential and Fermi level. The experimental data quantitatively agrees with previously documented charge exchange cross sections for thin films and shows the expected increase in the fraction of higher charge states with increasing velocity, over the ion velocity range considered. There is an observable material dependence of the charge state fraction. The measured charge state distributions are expressed as a mean charge state and compared with various mean and effective charge formalisms. The effective charge models are demonstrated to be inadequate representations of the measured mean charge states for the ions and films probed in this study.

The nuclear industry has used hard chromium plate for many years but is seeking alternatives, due to the adverse health effects of Cr(VI) employed in electroplating. In this study, testing and analysis regimes for the comparison of the sliding wear performance of candidate materials have been established and the performance of WC-(W,Cr)2C-Ni has been compared with that of hard chromium plate. WC-(W,Cr)2C-Ni was applied to Inconel 625 substrates using a detonation gun thermal spray technique. Sliding wear testing was performed using a ball-on-flat configuration reciprocating tribometer at 20 °C in three environments: dry, deionised water and simulated nuclear reactor water chemistry. Wear rates have been evaluated, using both mass and volume loss, and the worn samples were analysed using scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The WC-(W,Cr)2C-Ni coating had a broadly comparable wear performance to hard chromium plate in all three environments. There were differences between deionised and borated water, such that the latter needs to be used in further evaluation. SEM and XPS analyses enabled the wear mechanisms for WC-(W,Cr)2C-Ni and HCP to be elucidated, including pull-out and tribolayer formation. XPS has shown that the tribolayer on WC-(W,Cr)2C-Ni is stratified and undergoes chemical changes as a result of wear.

Off-Site Modular Construction (OSMC) research has been a burgeoning research area over the past two decades due to low productivity of traditional construction methods. Some large Gen 3 reactors may employ an on-site assembly area similar to shipbuilding techniques. This OSMC productivity has attracted the interest of the nuclear industry with over 50+ designs in commercial development. Off-site modular construction has been estimated to reduce the capital cost of an SMR by up to 37.98% compared to a stick-built method. The IAEA highlights the first commercial SMR “shop built and road transported to site” has an earliest operation date of 2026 (IAEA, 2018). This research paper aims to understand the current state of modular design in nuclear power by reviewing current literature with a systematic literature review. What can new small modular reactor designs learn from modularisation in large nuclear. What design and analysis techniques have been developed that may aid the design considering design, schedule, transportation and supply chain? What is the state of the art in the module design process? The research provides knowledge gaps and recommendations for further research.

Five new Tl(I) coordination compounds based on aryl monocyanoximes, such as phenylcyanoxime – HPhCO, 1, 2-fluorophenylcyanoxime – H(2F-PhCO, 2, 3-fluorophenylcyanoxime – H(3F-PhCO), 3, of TlL composition, and aryl biscyanoximes, such as 1,3-cyanoxime (benzene) – H2(1,3-BCO, 4 and 1,4-cyanoxime (benzene) – H2(1,4-BCO), 5 of Tl2L stoichiometry were synthesized and characterized using spectroscopic methods, thermal stability studies, and X-ray analysis. All obtained complexes represent coordination polymers of different complexity, ranging in dimensionality from 1D in Tl(2F-PhCO) to 3D in Tl2(1,3-BCO). The most interesting feature of all synthesized complexes is the formation of Tl2O2 rhombs: non planar and non-centrosymmetric in Tl(PhCO), and planar and centrosymmetric in the other three compounds. These rhombi are interconnected, forming zigzag and ladder-type polymers in which very short thallophilic Tl---Tl distances were observed. Thus, in the structure of Tl2(1,3-BCO) the closest distance between metal centers was found to be 3.670 A. This is the second shortest on-record intermetallic contact in non-organometallic and non-cluster, but Werner type complexes, and is close to that in metallic thallium: 3.456 A. In all five new coordination polymers the central atom has a stereo-active 6 s2 lone pair that significantly distorts the shape of the coordination polyhedron of Tl(I). The first time, Tl–O vibrations in Tl2O2 rhombs were observed in Raman spectra of the obtained complexes. Thermal analysis studies evidenced stability of all complexes, but Tl(PhCO), to ∼200 °C. The Tl2(1,3-BCO) compound demonstrates properties of the high energy compound, and violently exothermically decomposes at ∼255 °C with the release of a significant amount of kinetic energy. The final product of anaerobic decomposition of all studied Tl-cyanoximates is metallic thallium sponge.

The influence of high-energy (1.6 MeV) Ar2+ irradiation on the interfacial interaction between cerium oxide thin films (∼15 nm) with a SiO2/Si substrate is investigated using transmission electron microscopy, ultrahigh vacuum x-ray photoelectron spectroscopy (XPS), and a carbon monoxide (CO) oxidation catalytic reaction using ambient pressure XPS. The combination of these methods allows probing the dynamics of vacancy generation and its relation to chemical interactions at the CeO2/SiO2/Si interface. The results suggest that irradiation causes amorphization of some portion of CeO2 at the CeO2/SiO2/Si interface and creates oxygen vacancies due to the formation of Ce2O3 at room temperature. The subsequent ultra-high-vacuum annealing of irradiated films increases the concentration of Ce2O3 with the simultaneous growth of the SiO2 layer. Interactions with CO molecules result in an additional reduction of cerium and promote the transition of Ce2O3 to a silicate compound. Thermal annealing of thin films exposed to oxygen or carbon monoxide shows that the silicate phase is highly stabile even at 450 °C.

The UK Small Modular Reactor (UKSMR) programme has been established to develop an SMR for the UK energy market. Developing an SMR is a multi-disciplinary technical challenge, involving nuclear physics, electrical, mechanical, design, management, safety, testing to name but a few. In 2016 Upadhyay & Jain performed a literature review on modularity in Nuclear Power. They concluded that although modularisation has been utilised in nuclear to reduce costs, more work needs to be done to “create effective modules”. Hohmann et al also concluded the same for defining modules in the chemical process plant industry. The aim of this paper is to further define modules with a particular focus on an SMR for the UK market, the UKSMR. The methods highlighted may be relevant and applied to other international SMR designs or other types of plant. An overview and examination of modularisation work in nuclear to date is provided. The different configurations are defined for the Nuclear Steam Supply System (NSSS) in primary circuits and then for Balance of Plant (BOP) modules. A top level design process has been defined to aid in the understanding of design choices for current reactors and to further assist designing balance of plant modules. The paper then highlights areas for additional research that may further support module design and definition.

Reconfigurable mechanisms are a relatively recent contribution to the field of mechanism design and authors have only just been producing real-life applications of these mechanisms. This paper builds on the application of two categories of reconfigurable mechanisms by elaborating on a generalised static balancing theory suggested in a previous review paper [1]. These categories are single loop mechanisms with one degree of freedom per mode, and single loop mechanisms with multiple degrees of freedom per mode. In this paper it is shown that all configurations of the single DoF mechanisms can be balanced using a single spring. The multiple DoF mechanisms can be balanced by balancing each link with respect to the previous link. These balancing strategies are mathematically shown to be valid. The balancing strategy is then applied to a reconfigurable rehabilitation mechanism for patients with a lower limb paralysis by Tseng et al. [2] of which a simulation and a prototype is made to validate the theory. From the simulation and prototype follows that the single spring balancing of multiple configurations of a single DoF mechanism is possible.

Summary Meiosis produces gametes through a specialized, two-step cell division, which is highly error prone in humans. Reductional meiosis I, where maternal and paternal chromosomes (homologs) segregate, is followed by equational meiosis II, where sister chromatids separate. Uniquely during meiosis I, sister kinetochores are monooriented and pericentromeric cohesin is protected. Here, we demonstrate that these key adaptations for reductional chromosome segregation are achieved through separable control of multiple kinases by the meiosis-I-specific budding yeast Spo13 protein. Recruitment of Polo kinase to kinetochores directs monoorientation, while independently, cohesin protection is achieved by containing the effects of cohesin kinases. Therefore, reductional chromosome segregation, the defining feature of meiosis, is established by multifaceted kinase control by a master regulator. The recent identification of Spo13 orthologs, fission yeast Moa1 and mouse MEIKIN, suggests that kinase coordination by a meiosis I regulator may be a general feature in the establishment of reductional chromosome segregation., Graphical Abstract, Highlights • Spo13 recruits Polo kinase to kinetochores to direct sister chromatid co-segregation • Kinetochore-associated Polo drives co-segregation independently of monopolin • Spo13 counteracts cohesin kinases to prevent premature loss of centromeric cohesion • Spo13 restricts CK1δ to allow shugoshin reaccumulation after meiosis I, Segregation of homologs—rather than sister chromatids—is unique to meiosis I. Galander et al. show that the meiosis-I-specific Spo13 protein prevents sister chromatid segregation by controlling the effects of multiple kinases to both enforce sister kinetochore co-orientation and prevent premature loss of cohesion.

The half-life of the neutron-rich nuclide $^{60}\mathrm{Fe}$ has been in dispute in recent years. A measurement in 2009 published a value of $(2.62\ifmmode\pm\else\textpm\fi{}0.04)\ifmmode\times\else\texttimes\fi{}{10}^{6}$ years, almost twice that of the previously accepted value from 1984 of $(1.49\ifmmode\pm\else\textpm\fi{}0.27)\ifmmode\times\else\texttimes\fi{}{10}^{6}$ yr. This longer half-life was confirmed in 2015 by a second measurement, resulting in a value of $(2.50\ifmmode\pm\else\textpm\fi{}0.12)\ifmmode\times\else\texttimes\fi{}{10}^{6}$ yr. All three half-life measurements used the grow-in of the $\ensuremath{\gamma}$-ray lines in $^{60}\mathrm{Ni}$ from the decay of the ground state of $^{60}\mathrm{Co}$ (${t}_{1/2}=5.27$ yr) to determine the activity of a sample with a known number of $^{60}\mathrm{Fe}$ atoms. In contrast, the work presented here measured the $^{60}\mathrm{Fe}$ activity directly via the 58.6 keV $\ensuremath{\gamma}$-ray line from the short-lived isomeric state of $^{60}\mathrm{Co}$ (${t}_{1/2}=10.5$ min), thus being independent of any possible contamination from long-lived $^{60\mathrm{g}}\mathrm{Co}$. A fraction of the material from the 2015 experiment with a known number of $^{60}\mathrm{Fe}$ atoms was used for the activity measurement, resulting in a half-life value of $(2.72\ifmmode\pm\else\textpm\fi{}0.16)\ifmmode\times\else\texttimes\fi{}{10}^{6}$ yr, confirming again the longer half-life. In addition, $^{60}\mathrm{Fe}/^{56}\mathrm{Fe}$ isotopic ratios of samples with two different dilutions of this material were measured with accelerator mass spectrometry to determine the number of $^{60}\mathrm{Fe}$ atoms. Combining this with our activity measurement resulted in a half-life value of $(2.69\ifmmode\pm\else\textpm\fi{}0.28)\ifmmode\times\else\texttimes\fi{}{10}^{6}$ yr, again agreeing with the longer half-life.