43 research outputs found

    Uncertainties in atmospheric chemistry modelling due to convection parameterisations and subsequent scavenging

    Get PDF
    Moist convection in global modelling contributes significantly to the transport of energy, momentum, water and trace gases and aerosols within the troposphere. Since convective clouds are on a scale too small to be resolved in a global model their effects have to be parameterised. However, the whole process of moist convection and especially its parameterisations are associated with uncertainties. In contrast to previous studies on the impact of convection on trace gases, which had commonly neglected the convective transport for some or all compounds, we investigate this issue by examining simulations with five different convection schemes. This permits an uncertainty analysis due to the process formulation, without the inconsistencies inherent in entirely neglecting deep convection or convective tracer transport for one or more tracers. <br><br> Both the simulated mass fluxes and tracer distributions are analysed. Investigating the distributions of compounds with different characteristics, e.g., lifetime, chemical reactivity, solubility and source distributions, some differences can be attributed directly to the transport of these compounds, whereas others are more related to indirect effects, such as the transport of precursors, chemical reactivity in certain regions, and sink processes. <br><br> The model simulation data are compared with the average regional profiles of several measurement campaigns, and in detail with two campaigns in fall and winter 2005 in Suriname and Australia, respectively. <br><br> The shorter-lived a compound is, the larger the differences and consequently the uncertainty due to the convection parameterisation are, as long as it is not completely controlled by local production that is independent of convection and its impacts (e.g. water vapour changes). Whereas for long-lived compounds like CO or O<sub>3</sub> the mean differences between the simulations are less than 25%), differences for short-lived compounds reach up to ±100% with different convection schemes. <br><br> A rating of an overall "best" performing scheme is difficult, since the optimal performance depends on the region and compound

    The emission line near 1319 A in solar and stellar spectra

    Full text link
    An emission line near 1319 A is one of the strongest unidentified lines in the ultraviolet spectra of cool dwarf stars. In most line lists it is identified as a transition in N I, although its intensity would then be anomalous and the observed wavelength does not fit precisely that expected for N I. The line is also observed in cool giant stars. The measured wavelength of the line in stellar spectra is 1318.94 (+,- 0.01) A. Observations of giant stars provide further evidence that this line is not due to N I. It is proposed that this line is a decay from a previously unknown level in S I, which lies above the first ionization limit. This is identified with the 3d singlet D (odd parity) term. The previous tentative assignment of this term to the S I line at 1309.3 A then needs to be revised. The 1309.3 A line has been identified here for the first time in an astrophysical source. The singlet D (odd parity) level could, in principle, be populated by collisions from nearby autoionizing levels that have large number-densities, through population by di-electronic capture. Spin-orbit interaction with the autoionizing triplet D (odd parity) term might also lead to di-electronic capture into the singlet D (odd parity) level. A line at 1309.87 A observed in cool giant stars is identified as a transition in P II, pumped by the O I resonance lines.Comment: 9 pages, 3 figures, to be published in Monthly Notices of the Royal Astronomical Societ

    COSMOS2020: Identification of High-z Protocluster Candidates in COSMOS

    Full text link
    We conduct a systematic search for protocluster candidates at z6z \geq 6 in the COSMOS field using the recently released COSMOS2020 source catalog. We select galaxies using a number of selection criteria to obtain a sample of galaxies that have a high probability of being inside a given redshift bin. We then apply overdensity analysis to the bins using two density estimators, a Weighted Adaptive Kernel Estimator and a Weighted Voronoi Tessellation Estimator. We have found 15 significant (>4σ>4\sigma) candidate galaxy overdensities across the redshift range 6z7.76\le z\le7.7. The majority of the galaxies appear to be on the galaxy main sequence at their respective epochs. We use multiple stellar-mass-to-halo-mass conversion methods to obtain a range of dark matter halo mass estimates for the overdensities in the range of 101113M\sim10^{11-13}\,M_{\rm \odot}, at the respective redshifts of the overdensities. The number and the masses of the halos associated with our protocluster candidates are consistent with what is expected from the area of a COSMOS-like survey in a standard Λ\LambdaCDM cosmology. Through comparison with simulation, we expect that all the overdensities at z6z\simeq6 will evolve into a Virgo-/Coma-like clusters at present (i.e., with masses 10141015M\sim 10^{14}-10^{15}\,M_{\rm \odot}). Compared to other overdensities identified at z6z \geq 6 via narrow-band selection techniques, the overdensities presented appear to have 10×\sim10\times higher stellar masses and star-formation rates. We compare the evolution in the total star-formation rate and stellar mass content of the protocluster candidates across the redshift range 6z7.76\le z\le7.7 and find agreement with the total average star-formation rate from simulations.Comment: 52 pages, 32 figues, 18 tables, main text is 30 pages, appendix is 22 pages, to be published in Ap

    The Ultraviolet Luminosity Function at 0.6 < z < 1 from UVCANDELS

    Get PDF
    © 2024. The Author(s). Published by the American Astronomical Society. This work is licensed under the terms of under the terms of the Creative Commons Attribution 4.0 licence: https://creativecommons.org/licenses/by/4.0/UVCANDELS is a Hubble Space Telescope Cycle-26 Treasury Program awarded 164 orbits of primary ultraviolet (UV) F275W imaging and coordinated parallel optical F435W imaging in four CANDELS fields—GOODS-N, GOODS-S, EGS, and COSMOS—covering a total area of ∼426 arcmin2. This is ∼2.7 times larger than the area covered by previous deep-field space UV data combined, reaching a depth of about 27 and 28 ABmag (5σ in 0.”2 apertures) for F275W and F435W, respectively. Along with new photometric catalogs, we present an analysis of the rest-frame UV luminosity function (LF), relying on our UV-optimized aperture photometry method, yielding a factor of 1.5 increase over H-isophot aperture photometry in the signal-to-noise ratios of galaxies in our F275W imaging. Using well-tested photometric redshift measurements, we identify 5810 galaxies at redshifts 0.6 < z < 1, down to an absolute magnitude of M UV = −14.2. In order to minimize the effect of uncertainties in estimating the completeness function, especially at the faint end, we restrict our analysis to sources above 30% completeness, which provides a final sample of 4726 galaxies at −21.5 < M UV < −15.5. We performed a maximum likelihood estimate to derive the best-fit parameters of the UV LF. We report a best-fit faint-end slope of α=−1.359−0.041+0.041 at z ∼ 0.8. Creating subsamples at z ∼ 0.7 and z ∼ 0.9, we observe a possible evolution of α with redshift. The unobscured UV luminosity density at M UV < −10 is derived as ρUV=1.339−0.030+0.027(×1026ergs−1Hz−1Mpc−3) using our best-fit LF parameters. The new F275W and F435 photometric catalogs from UVCANDELS have been made publicly available on the Barbara A. Mikulski Archive for Space Telescopes.Peer reviewe

    Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth

    Get PDF
    Background The onset of birth in humans, like other apes, differs from non-primate mammals in its endocrine physiology. We hypothesize that higher primate-specific gene evolution may lead to these differences and target genes involved in human preterm birth, an area of global health significance. Methods We performed a comparative genomics screen of highly conserved noncoding elements and identified PLA2G4C, a phospholipase A isoform involved in prostaglandin biosynthesis as human accelerated. To examine whether this gene demonstrating primate-specific evolution was associated with birth timing, we genotyped and analyzed 8 common single nucleotide polymorphisms (SNPs) in PLA2G4C in US Hispanic (n = 73 preterm, 292 control), US White (n = 147 preterm, 157 control) and US Black (n = 79 preterm, 166 control) mothers. Results Detailed structural and phylogenic analysis of PLA2G4C suggested a short genomic element within the gene duplicated from a paralogous highly conserved element on chromosome 1 specifically in primates. SNPs rs8110925 and rs2307276 in US Hispanics and rs11564620 in US Whites were significant after correcting for multiple tests (p < 0.006). Additionally, rs11564620 (Thr360Pro) was associated with increased metabolite levels of the prostaglandin thromboxane in healthy individuals (p = 0.02), suggesting this variant may affect PLA2G4C activity. Conclusions Our findings suggest that variation in PLA2G4C may influence preterm birth risk by increasing levels of prostaglandins, which are known to regulate labor.Children’s Discovery InstituteMarch of Dimes Birth Defects FoundationNational Institute of General Medical Sciences (U.S.) (grant T32 GM081739)Washington University (Saint Louis, Mo.) (Mr. and Mrs. Spencer T. Olin Fellowship for Women in Graduate Study)Sigrid Jusélius FoundationSigne and Anne Gyllenberg FoundationAcademy of FinlandVanderbilt University (Turner-Hazinski grant award

    The Lyman Continuum Escape Fraction of Star-forming Galaxies at 2.4z3.72.4\lesssim z\lesssim3.7 from UVCANDELS

    Full text link
    The UltraViolet Imaging of the Cosmic Assembly Near-infrared Deep Extragalactic Legacy Survey Fields (UVCANDELS) survey is a Hubble Space Telescope (HST) Cycle-26 Treasury Program, allocated in total 164 orbits of primary Wide-Field Camera 3 Ultraviolet and Visible light F275W imaging with coordinated parallel Advanced Camera for Surveys F435W imaging, on four of the five premier extragalactic survey fields: GOODS-N, GOODS-S, EGS, and COSMOS. We introduce this survey by presenting a thorough search for galaxies at z2.4z\gtrsim2.4 that leak significant Lyman continuum (LyC) radiation, as well as a stringent constraint on the LyC escape fraction (fescf_{\rm esc}) from stacking the UV images of a population of star-forming galaxies with secure redshifts. Our extensive search for LyC emission and stacking analysis benefit from the catalogs of high-quality spectroscopic redshifts compiled from archival ground-based data and HST slitless spectroscopy, carefully vetted by dedicated visual inspection efforts. We report a sample of five galaxies as individual LyC leaker candidates, showing fescrel60%f_{\rm esc}^{\rm rel}\gtrsim60\% estimated using detailed Monte Carlo analysis of intergalactic medium attenuation. We develop a robust stacking method to apply to five samples of in total 85 non-detection galaxies in the redshift range of z[2.4,3.7]z\in[2.4,3.7]. Most stacks give tight 2-σ\sigma upper limits below fescrel<6%f_{\rm esc}^{\rm rel}<6\%. A stack for a subset of 32 emission-line galaxies shows tentative LyC leakage detected at 2.9-σ\sigma, indicating fescrel=5.7%f_{\rm esc}^{\rm rel}=5.7\% at z2.65z\sim2.65, supporting the key role of such galaxies in contributing to the cosmic reionization and maintaining the UV ionization background. These new F275W and F435W imaging mosaics from UVCANDELS have been made publicly available on the Barbara A. Mikulski Archive for Space Telescopes.Comment: 33 pages, 21 figures, and 5 tables. Resubmitted after addressing the referee repor

    Recent genomic heritage in Scotland

    Get PDF
    BACKGROUND: The Generation Scotland Scottish Family Health Study (GS:SFHS) includes 23,960 participants from across Scotland with records for many health-related traits and environmental covariates. Genotypes at ~700 K SNPs are currently available for 10,000 participants. The cohort was designed as a resource for genetic and health related research and the study of complex traits. In this study we developed a suite of analyses to disentangle the genomic differentiation within GS:SFHS individuals to describe and optimise the sample and methods for future analyses. RESULTS: We combined the genotypic information of GS:SFHS with 1092 individuals from the 1000 Genomes project and estimated their genomic relationships. Then, we performed Principal Component Analyses of the resulting relationships to investigate the genomic origin of different groups. We characterised two groups of individuals: those with a few sparse rare markers in the genome, and those with several large rare haplotypes which might represent relatively recent exogenous ancestors. We identified some individuals with likely Italian ancestry and a group with some potential African/Asian ancestry. An analysis of homozygosity in the GS:SFHS sample revealed a very similar pattern to other European populations. We also identified an individual carrying a chromosome 1 uniparental disomy. We found evidence of local geographic stratification within the population having impact on the genomic structure. CONCLUSIONS: These findings illuminate the history of the Scottish population and have implications for further analyses such as the study of the contributions of common and rare variants to trait heritabilities and the evaluation of genomic and phenotypic prediction of disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1605-2) contains supplementary material, which is available to authorized users

    Effects of plant diversity, habitat and agricultural landscape structure on the functional diversity of carabid assemblages in the North China Plain

    Get PDF
    1. This study investigated the effects of plant diversity, habitat type and landscape structure on the functional diversity of the carabid assemblages in the agro-landscape of the North China Plain. We hypothesize (i) small, herbivorous and omnivorous carabids are more strongly affected by local plant diversity, while large and predatory carabids are strongly affected by landscape structure, and (ii) habitat type influences the diversity across functional groups. 2. In 2010, carabid beetles were sampled by pitfall traps in 6 typical habitats of the agro-landscape: wheat/maize fields, peanut fields, orchards, field margins, windbreaks and woodland. 3. Our results showed that (i) habitat type played a predominant role in driving the changes in the diversity of carabid assemblages, followed by local plant diversity while the landscape structure had little effect; (ii) small and omnivorous carabid were strongly affected by local plant diversity, while the composition of large and predatory carabid was strongly associated with the landscape structure; and (iii) habitats dominated by woody species harbored different assemblages to habitats dominated by herbaceous plants for overall carabids and three functional groups excluding omnivorous beetles. 4. Informed by our results, we suggest the differentiated responses between functional groups should be appreciated in conservation management. In the intensively managed agro-landscape, maintenance of diverse habitats and creating a more complex vegetation structure would be the most efficient measures to enhance the diversity of carabid assemblages. Particularly, the maintenance of extensively managed habitats coupled with a targeted increase in the local plant diversity is crucial to optimize the biological pest-control by carabid assemblages

    Efficacy and safety of autologous haematopoietic stem cell transplantation versus alemtuzumab, ocrelizumab, ofatumumab or cladribine in relapsing remitting multiple sclerosis (StarMS): protocol for a randomised controlled trial

    Get PDF
    Introduction: Autologous haematopoietic stem cell transplantation (aHSCT) is increasingly used as treatment for patients with active multiple sclerosis (MS), typically after failure of disease-modifying therapies (DMTs). A recent phase III trial, ‘Multiple Sclerosis International Stem Cell Transplant, MIST’, showed that aHSCT resulted in prolonged time to disability progression compared with DMTs in patients with relapsing remitting MS (RRMS). However, the MIST trial did not include many of the current high-efficacy DMTs (alemtuzumab, ocrelizumab, ofatumumab or cladribine) in use in the UK within the control arm, which are now offered to patients with rapidly evolving severe MS (RES-MS) who are treatment naïve. There remain, therefore, unanswered questions about the relative efficacy and safety of aHSCT over these high-efficacy DMTs in these patient groups. The StarMS trial (Autologous Stem Cell Transplantation versus Alemtuzumab, Ocrelizumab, Ofatumumab or Cladribine in Relapsing Remitting Multiple Sclerosis) will assess the efficacy, safety and long-term impact of aHSCT compared with high-efficacy DMTs in patients with highly active RRMS despite the use of standard DMTs or in patients with treatment naïve RES-MS. Methods and analysis: StarMS is a multicentre parallel-group rater-blinded randomised controlled trial with two arms. A total of 198 participants will be recruited from 19 regional neurology secondary care centres in the UK. Participants will be randomly allocated to the aHSCT arm or DMT arm in a 1:1 ratio. Participants will remain in the study for 2 years with follow-up visits at 3, 6, 9, 12, 18 and 24 months postrandomisation. The primary outcome is the proportion of patients who achieve ‘no evidence of disease activity’ during the 2-year postrandomisation follow-up period in an intention to treat analysis. Secondary outcomes include efficacy, safety, cost-effectiveness and immune reconstitution of aHSCT and the four high-efficacy DMTs. Ethics and dissemination: The study was approved by the Yorkshire and Humber—Leeds West Research Ethics Committee (20/YH/0061). Participants will provide written informed consent prior to any study specific procedures. The study results will be submitted to a peer-reviewed journal and abstracts will be submitted to relevant national and international conferences. Trial registration number: ISRCTN88667898
    corecore