High-contrast observations of brown dwarf companion HR 2562 B with the vector Apodizing Phase Plate coronagraph

InstrumentationStars and planetary system

What is the Nature of EUV Waves? First STEREO 3D Observations and Comparison with Theoretical Models

One of the major discoveries of the Extreme ultraviolet Imaging Telescope (EIT) on SOHO were intensity enhancements propagating over a large fraction of the solar surface. The physical origin(s) of the so-called `EIT' waves is still strongly debated. They are considered to be either wave (primarily fast-mode MHD waves) or non-wave (pseudo-wave) interpretations. The difficulty in understanding the nature of EUV waves lies with the limitations of the EIT observations which have been used almost exclusively for their study. Their limitations are largely overcome by the SECCHI/EUVI observations on-board the STEREO mission. The EUVI telescopes provide high cadence, simultaneous multi-temperature coverage, and two well-separated viewpoints. We present here the first detailed analysis of an EUV wave observed by the EUVI disk imagers on December 07, 2007 when the STEREO spacecraft separation was $\approx 45^\circ$. Both a small flare and a CME were associated with the wave cadence, and single temperature and viewpoint coverage. These limitations are largely overcome by the SECCHI/EUVI observations on-board the STEREO mission. The EUVI telescopes provide high cadence, simultaneous multi-temperature coverage, and two well-separated viewpoints. Our findings give significant support for a fast-mode interpretation of EUV waves and indicate that they are probably triggered by the rapid expansion of the loops associated with the CME.Comment: Solar Physics, 2009, Special STEREO Issue, in pres

Partial wave analysis of J/\psi \to \gamma \phi \phi

Using $5.8 \times 10^7 J/\psi$ events collected in the BESII detector, the radiative decay $J/\psi \to \gamma \phi \phi \to \gamma K^+ K^- K^0_S K^0_L$ is studied. The $\phi\phi$ invariant mass distribution exhibits a near-threshold enhancement that peaks around 2.24 GeV/$c^{2}$. A partial wave analysis shows that the structure is dominated by a $0^{-+}$ state ($\eta(2225)$) with a mass of $2.24^{+0.03}_{-0.02}{}^{+0.03}_{-0.02}$ GeV/$c^{2}$ and a width of $0.19 \pm 0.03^{+0.06}_{-0.04}$ GeV/$c^{2}$. The product branching fraction is: $Br(J/\psi \to \gamma \eta(2225))\cdot Br(\eta(2225)\to \phi\phi) = (4.4 \pm 0.4 \pm 0.8)\times 10^{-4}$.Comment: 11 pages, 4 figures. corrected proof for journa

A multi-parent advanced generation inter-cross (MAGIC) population for genetic analysis and improvement of cowpea (Vigna unguiculata L. Walp.)

Published online: 21 Jan 2018Multi‐parent advanced generation inter‐cross (MAGIC) populations are an emerging type of resource for dissecting the genetic structure of traits and improving breeding populations. We developed a MAGIC population for cowpea (Vigna unguiculata L. Walp.) from eight founder parents. These founders were genetically diverse and carried many abiotic and biotic stress resistance, seed quality and agronomic traits relevant to cowpea improvement in the United States and sub‐Saharan Africa, where cowpea is vitally important in the human diet and local economies. The eight parents were inter‐crossed using structured matings to ensure that the population would have balanced representation from each parent, followed by single‐seed descent, resulting in 305 F8 recombinant inbred lines each carrying a mosaic of genome blocks contributed by all founders. This was confirmed by single nucleotide polymorphism genotyping with the Illumina Cowpea Consortium Array. These lines were on average 99.74% homozygous but also diverse in agronomic traits across environments. Quantitative trait loci (QTLs) were identified for several parental traits. Loci with major effects on photoperiod sensitivity and seed size were also verified by biparental genetic mapping. The recombination events were concentrated in telomeric regions. Due to its broad genetic base, this cowpea MAGIC population promises breakthroughs in genetic gain, QTL and gene discovery, enhancement of breeding populations and, for some lines, direct releases as new varieties

Study of J/Psi decays into eta Kstar Kstar-bar

We report the first observation of \mPJpsi \to \mPeta\mPKst\mAPKst decay in a \mPJpsi sample of 58 million events collected with the BESII detector. The branching fraction is determined to be $(1.15 \pm 0.13 \pm 0.22)\times 10^{-3}$. The selected signal event sample is further used to search for the \mPY resonance through \mPJpsi \to \mPeta \mPY, \mPY\to\mPKst\mAPKst. No evidence of a signal is seen. An upper limit of \mathrm{Br}(\mPJpsi \to \mPeta \mPY)\cdot\mathrm{Br}(\mPY\to\mPKst\mAPKst) < 2.52\times 10^{-4} is set at the 90% confidence level.Comment: 11 pages, 4 figure

Vector-apodizing phase plate coronagraph: design, current performance, and future development [Invited]

Instrumentatio

Understorey thinning and burning trials are needed in conservation reserves: The case of Tuart (Eucalyptus gomphocephala D.C.)

Management interventions are needed to reverse the decline of Tuart (Eucalyptus gomphocephala) woodland in the Yalgorup area of south-west Western Australia where the largest intact remaining example of this ecosystem is located. Although the cause of the decline is uncertain and several factors may be involved, management action should not be withheld because the decline process is not fully understood. We contend that the reduction in fire frequency over the last 50 years has led to an increase in understorey density, particularly of Western Australian Peppermint (Agonis flexuosa), resulting in greater competition for resources, which may in turn have increased the susceptibility of healthy woodland to decline. In contrast to Tuart regeneration, which is usually tied to fire, Western Australian Peppermint can establish readily in unburnt woodland. Further, once Western Australian Peppermint seedlings develop to the lignotuberous stage, they can resprout vigorously after fire. Therefore, a combination of fire and the physical removal of understorey in sites where this species has formed extensive thickets is required to: (i) provide an opportunity for regeneration of Tuart in both healthy and declining stands; (ii) improve the chances of sustained recovery of Tuart trees in declining stands; and (iii) ensure heterogeneity in the vegetation at multiple scales, a recognized strategy for conserving biodiversity and increasing ecosystem resilience. We propose that this approach may also be relevant to other tree decline syndromes in southern Australia. However, fostering community support for active intervention using thinning and fire in conservation reserves and staging the operations within an experimental framework will be important for such action to gain both the social and scientific acceptance necessary for it to be applied widely

Novel methods for managing freshwater refuges against climate change in southern Australia

Southern Australia is becoming warmer and drier as climate change progresses, creating serious threats to freshwater ecosystems that are dependent on the presence of water for their existence. The overall aim of this research project was to develop and evaluate four potential methods for enhancing the role, function and resilience of refuges for freshwater biodiversity in southern Australia. It focussed on means to maintain the physical conditions in refuges within ranges tolerable for species and to maintain connectivity that allows species to retreat to, and expand from, refuges. The four approaches studied were: • the feasibility of using cool-water releases (CWR) from reservoirs and shandying to control water temperature in rivers; • a method for deciding where streamside re-vegetation should occur in catchments to ensure maximum long-term negative effects on stream temperature; • the potential for artificial urban wetlands (i.e. anthropogenic habitat) to act as refuges for freshwater biodiversity against climate change; • a method for identifying redundant river regulation infrastructure and prioritizing artificial structures for removal during river restoration to improve connectivity along river channels for fauna movement. These four approaches were found to have the potential to address a range of objectives for refuge management, such as: reduce temperatures in refuges (1 & 2), increase number of refuges that act as colonization sources (all), assist dispersal into and out of refuges (all), increase biodiversity within refuges (all), increase permanence or resilience of refuges (all) and increase resistance or resilience of refuges during extreme events (1, 2 & 3). In particular, CWR could potentially be used to mimic natural thermal regimes, reduce the frequency and duration of extreme high temperature events and to assist movement of fish between thermal refuges, but further information and trials are required (1). Riparian planting can be used to reduce in-stream temperatures over the long-term and the tool developed here permits users to determine the optimal planting locations within catchments to maximise cooling effects for a given replanting investment (2). Perennial artificial wetlands can be used to provide refuges for biodiversity from wetland drying, and artificial wetlands can be modified to support higher biodiversity (3). The removal or modification of in-stream barriers can be used to create, protect or link refuges for freshwater species, especially fish, and the method developed here allows users to determine which artificial barriers have priority for removal within catchments (4). There are synergies with catchment restoration, such as environmental flows (CWR, barrier removal and modification), and revegetation (riparian replanting, anthropogenic refuges).Therefore, the four refuge management approaches described in this project should be integrated into existing river and wetland restoration practices within catchments. Refuges across all types of waterbodies in catchments should be managed in an integrated way, comprising multiple waterbodies of each type to provide the diversity of habitat types required by freshwater species