1,950 research outputs found

    All-Optical Nanopositioning of High-Q Silica Microspheres

    Get PDF
    A tunable, all-optical, coupling method has been realized for a high-\textit{Q} silica microsphere and an optical waveguide. By means of a novel optical nanopositioning method, induced thermal expansion of an asymmetric microsphere stem for laser powers up to 171~mW has been observed and used to fine tune the microsphere-waveguide coupling. Microcavity displacements ranging from (0.612~±\pm~0.13) -- (1.5 ±\pm 0.13) Ό\mum and nanometer scale sensitivities varying from (2.81 ±\pm 0.08) -- (7.39 ±\pm 0.17) nm/mW, with an apparent linear dependency of coupling distance on stem laser heating, were obtained. Using this method, the coupling was altered such that different coupling regimes could be explored for particular samples. This tunable coupling method, in principle, could be incorporated into lab-on-a-chip microresonator systems, photonic molecule systems, and other nanopositioning frameworks.Comment: 6pages,4figure

    The Evolution of Active Droplets in Chemorobotic Platforms

    Get PDF
    There is great interest in oil-in-water droplets as simple systems that display astonishingly complex behaviours. Recently, we reported a chemorobotic platform capable of autonomously exploring and evolving the behaviours these droplets can exhibit. The platform enabled us to undertake a large number of reproducible experiments, allowing us to probe the non-linear relationship between droplet composition and behaviour. Herein we introduce this work, and also report on the recent developments we have made to this system. These include new platforms to simultaneously evolve the droplets’ physical and chemical environments and the inclusion of selfreplicating molecules in the droplets

    Evolutionary Models for Formation of Network Motifs and Modularity in the Saccharomyces Transcription Factor Network

    Get PDF
    Many natural and artificial networks contain overrepresented subgraphs, which have been termed network motifs. In this article, we investigate the processes that led to the formation of the two most common network motifs in eukaryote transcription factor networks: the bi-fan motif and the feed-forward loop. Around 100 million y ago, the common ancestor of the Saccharomyces clade underwent a whole-genome duplication event. The simultaneous duplication of the genes created by this event enabled the origin of many network motifs to be established. The data suggest that there are two primary mechanisms that are involved in motif formation. The first mechanism, enabled by the substantial plasticity in promoter regions, is rewiring of connections as a result of positive environmental selection. The second is duplication of transcription factors, which is also shown to be involved in the formation of intermediate-scale network modularity. These two evolutionary processes are complementary, with the pre-existence of network motifs enabling duplicated transcription factors to bind different targets despite structural constraints on their DNA-binding specificities. This process may facilitate the creation of novel expression states and the increases in regulatory complexity associated with higher eukaryotes

    Mechanical design principles of a mitotic spindle.

    Get PDF
    An organised spindle is crucial to the fidelity of chromosome segregation, but the relationship between spindle structure and function is not well understood in any cell type. The anaphase B spindle in fission yeast has a slender morphology and must elongate against compressive forces. This 'pushing' mode of chromosome transport renders the spindle susceptible to breakage, as observed in cells with a variety of defects. Here we perform electron tomographic analyses of the spindle, which suggest that it organises a limited supply of structural components to increase its compressive strength. Structural integrity is maintained throughout the spindle's fourfold elongation by organising microtubules into a rigid transverse array, preserving correct microtubule number and dynamically rescaling microtubule length

    Hydantoin-bridged medium ring scaffolds by migratory insertion of urea-tethered nitrile anions into aromatic C-N bonds

    Get PDF
    Bicyclic or tricyclic nitrogen-containing heterocyclic scaffolds were constructed rapidly by intramolecular nucleophilic aromatic substitution of metallated nitriles tethered by a urea linkage to a series of electronically unactivated heterocyclic precursors. The substitution reaction constitutes a ring expansion, enabled by the conformationally constrained tether between the nitrile and the heterocycle. Attack of the metallated urea leaving group on the nitrile generates a hydantoin that bridges the polycyclic products. X-ray crystallography reveals ring-dependant strain within the hydantoin

    Rethinking rewilding: A response to JĂžrgensen

    Get PDF
    In this article we respond to and challenge Jþrgensen’s criticisms of the concept of rewilding in her paper ‘Rethinking rewilding’, published this year in Geoforum. Jþrgensen argues that ‘rewilding’ has become a ‘plastic word’, one that has been stretched to the point where it lacks definitional precision, at risk of becoming ‘the go-to blanket solution to environmental problems’. She also argues that the practice of rewilding is premised upon the dissociation of humans from the rest of nature and reproduces anti-human Nature–Culture binaries, rightly lambasted by critics of wilderness narratives in conservation practice. In response to these criticisms we challenge Jþrgensen on two points. Firstly we argue that the problems of ‘plasticity’ and definitional imprecision can be rectified by highlighting and foregrounding the quality that we believe is at the core of all rewilding definitions and efforts: non-human autonomy. Secondly, we challenge Jþrgensen’s broad claim that sees the collapse of ‘rewilding’ into anti-human wilderness management. We do so by reflecting on two points; the dynamic human–non-human entanglements embedded within rewilding practice(s) and by arguing for rewilding as a ‘wild experiment’. We make these points through the examination of two actually existing examples of rewilding
    • 

    corecore