755 research outputs found

    Morfologia e portamento nella quercia da sughero (<i>Quercus suber</i> L.) in Sardegna

    Get PDF
    I principali parametri ambientali che, nel corso del tempo, modellano la forma di una pianta arborea sono la luce, la disponibilità idrica e di nutrienti, la temperatura, la gravità, il vento, i rapporti con le altre specie. Le piante legnose, nel corso della loro vita, sono inoltre costantemente soggette a stress come compressioni e tensioni causate da tassi di crescita differenziati nei diversi tessuti, aumenti annuali della fitomassa totale ed effetti di reazione alla spinta del vento. Nel caso particolare della sughera, altri importanti fattori che ne determinano la morfologia ed il portamento sono il fuoco, la defogliazione, la brucatura da parte degli erbivori, le operazioni di potatura, la decortica. Dall'analisi complessiva risulta evidente come il portamento in apparenza naturale di Quercus suber L. è fortemente condizionato, nelle sue più diverse espressioni, dai fattori ambientali

    Epigenetic diversity of clonal white poplar (<i>Populus alba</i> L.) populations: could methylation support the success of vegetative reproduction strategy?

    Get PDF
    The widespread poplar populations of Sardinia are vegetatively propagated and live in different natural environments forming large monoclonal stands. The main goals of the present study were: i) to investigate/measure the epigenetic diversity of the poplar populations by determining their DNA methylation status; ii) to assess if and how methylation status influences population clustering; iii) to shed light on the changes that occur in the epigenome of ramets of the same poplar clone. To these purposes, 83 white poplar trees were sampled at different locations on the island of Sardinia. Methylation sensitive amplified polymorphism analysis was carried out on the genomic DNA extracted from leaves at the same juvenile stage. The study showed that the genetic biodiversity of poplars is quite limited but it is counterbalanced by epigenetic inter-population molecular variability. The comparison between MspI and HpaII DNA fragmentation profiles revealed that environmental conditions strongly influence hemi-methylation of the inner cytosine. The variable epigenetic status of Sardinian white poplars revealed a decreased number of population clusters. Landscape genetics analyses clearly demonstrated that ramets of the same clone were differentially methylated in relation to their geographic position. Therefore, our data support the notion that studies on plant biodiversity should no longer be restricted to genetic aspects, especially in the case of vegetatively propagated plant species

    A Contribution to the study of the distribution of <i>Medicago-Sinorhizobium</i> symbiosis in Sardinia (Italy)

    Get PDF
    The paper summarizes the results of a Medicago-Sinorhizobium germplasm survey and collection carried out in the island of Sardinia (Italy) in 1998/99 and subsequent laboratory isolation of microbial strains, soil sample analyses and determination of Medicago species. According to a stratified sampling methodology, the major ecological characteristics of island's habitats were taken into account, collecting and surveying mostly in natural or semi-natural habitats (no roadside sites nor cultivated fields were sampled). Forty-six sites, widely distributed in semi-natural representative areas of Sardinia, ranging from sea level to above 1000 m asl, were sampled and 24 were surveyed to gather additional data on species distribution. Root nodules were collected from 15 species (13 annuals) out of the total 21 Medicago species recorded in Sardinia. Isolation of root nodule bacteria accessions and identification of 29 strains were achieved. A total number of 17 species were surveyed and mapped. The present study gives a first contribution to the knowledge of the present distribution of the species of the genus Medicago in Sardinia with special concern to the species recorded or sampled during the survey and highlights the presence of Medicago biodiversity hot spots

    LHCb upgrade software and computing : technical design report

    Get PDF
    This document reports the Research and Development activities that are carried out in the software and computing domains in view of the upgrade of the LHCb experiment. The implementation of a full software trigger implies major changes in the core software framework, in the event data model, and in the reconstruction algorithms. The increase of the data volumes for both real and simulated datasets requires a corresponding scaling of the distributed computing infrastructure. An implementation plan in both domains is presented, together with a risk assessment analysis

    Physics case for an LHCb Upgrade II - Opportunities in flavour physics, and beyond, in the HL-LHC era

    Get PDF
    The LHCb Upgrade II will fully exploit the flavour-physics opportunities of the HL-LHC, and study additional physics topics that take advantage of the forward acceptance of the LHCb spectrometer. The LHCb Upgrade I will begin operation in 2020. Consolidation will occur, and modest enhancements of the Upgrade I detector will be installed, in Long Shutdown 3 of the LHC (2025) and these are discussed here. The main Upgrade II detector will be installed in long shutdown 4 of the LHC (2030) and will build on the strengths of the current LHCb experiment and the Upgrade I. It will operate at a luminosity up to 2×1034 cm−2s−1, ten times that of the Upgrade I detector. New detector components will improve the intrinsic performance of the experiment in certain key areas. An Expression Of Interest proposing Upgrade II was submitted in February 2017. The physics case for the Upgrade II is presented here in more depth. CP-violating phases will be measured with precisions unattainable at any other envisaged facility. The experiment will probe b → sl+l−and b → dl+l− transitions in both muon and electron decays in modes not accessible at Upgrade I. Minimal flavour violation will be tested with a precision measurement of the ratio of B(B0 → μ+μ−)/B(Bs → μ+μ−). Probing charm CP violation at the 10−5 level may result in its long sought discovery. Major advances in hadron spectroscopy will be possible, which will be powerful probes of low energy QCD. Upgrade II potentially will have the highest sensitivity of all the LHC experiments on the Higgs to charm-quark couplings. Generically, the new physics mass scale probed, for fixed couplings, will almost double compared with the pre-HL-LHC era; this extended reach for flavour physics is similar to that which would be achieved by the HE-LHC proposal for the energy frontier

    Multidifferential study of identified charged hadron distributions in ZZ-tagged jets in proton-proton collisions at s=\sqrt{s}=13 TeV

    Full text link
    Jet fragmentation functions are measured for the first time in proton-proton collisions for charged pions, kaons, and protons within jets recoiling against a ZZ boson. The charged-hadron distributions are studied longitudinally and transversely to the jet direction for jets with transverse momentum 20 <pT<100< p_{\textrm{T}} < 100 GeV and in the pseudorapidity range 2.5<η<42.5 < \eta < 4. The data sample was collected with the LHCb experiment at a center-of-mass energy of 13 TeV, corresponding to an integrated luminosity of 1.64 fb1^{-1}. Triple differential distributions as a function of the hadron longitudinal momentum fraction, hadron transverse momentum, and jet transverse momentum are also measured for the first time. This helps constrain transverse-momentum-dependent fragmentation functions. Differences in the shapes and magnitudes of the measured distributions for the different hadron species provide insights into the hadronization process for jets predominantly initiated by light quarks.Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-013.html (LHCb public pages

    Study of the BΛc+ΛˉcKB^{-} \to \Lambda_{c}^{+} \bar{\Lambda}_{c}^{-} K^{-} decay

    Full text link
    The decay BΛc+ΛˉcKB^{-} \to \Lambda_{c}^{+} \bar{\Lambda}_{c}^{-} K^{-} is studied in proton-proton collisions at a center-of-mass energy of s=13\sqrt{s}=13 TeV using data corresponding to an integrated luminosity of 5 fb1\mathrm{fb}^{-1} collected by the LHCb experiment. In the Λc+K\Lambda_{c}^+ K^{-} system, the Ξc(2930)0\Xi_{c}(2930)^{0} state observed at the BaBar and Belle experiments is resolved into two narrower states, Ξc(2923)0\Xi_{c}(2923)^{0} and Ξc(2939)0\Xi_{c}(2939)^{0}, whose masses and widths are measured to be m(Ξc(2923)0)=2924.5±0.4±1.1MeV,m(Ξc(2939)0)=2938.5±0.9±2.3MeV,Γ(Ξc(2923)0)=0004.8±0.9±1.5MeV,Γ(Ξc(2939)0)=0011.0±1.9±7.5MeV, m(\Xi_{c}(2923)^{0}) = 2924.5 \pm 0.4 \pm 1.1 \,\mathrm{MeV}, \\ m(\Xi_{c}(2939)^{0}) = 2938.5 \pm 0.9 \pm 2.3 \,\mathrm{MeV}, \\ \Gamma(\Xi_{c}(2923)^{0}) = \phantom{000}4.8 \pm 0.9 \pm 1.5 \,\mathrm{MeV},\\ \Gamma(\Xi_{c}(2939)^{0}) = \phantom{00}11.0 \pm 1.9 \pm 7.5 \,\mathrm{MeV}, where the first uncertainties are statistical and the second systematic. The results are consistent with a previous LHCb measurement using a prompt Λc+K\Lambda_{c}^{+} K^{-} sample. Evidence of a new Ξc(2880)0\Xi_{c}(2880)^{0} state is found with a local significance of 3.8σ3.8\,\sigma, whose mass and width are measured to be 2881.8±3.1±8.5MeV2881.8 \pm 3.1 \pm 8.5\,\mathrm{MeV} and 12.4±5.3±5.8MeV12.4 \pm 5.3 \pm 5.8 \,\mathrm{MeV}, respectively. In addition, evidence of a new decay mode Ξc(2790)0Λc+K\Xi_{c}(2790)^{0} \to \Lambda_{c}^{+} K^{-} is found with a significance of 3.7σ3.7\,\sigma. The relative branching fraction of BΛc+ΛˉcKB^{-} \to \Lambda_{c}^{+} \bar{\Lambda}_{c}^{-} K^{-} with respect to the BD+DKB^{-} \to D^{+} D^{-} K^{-} decay is measured to be 2.36±0.11±0.22±0.252.36 \pm 0.11 \pm 0.22 \pm 0.25, where the first uncertainty is statistical, the second systematic and the third originates from the branching fractions of charm hadron decays.Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-028.html (LHCb public pages

    Measurement of the ratios of branching fractions R(D)\mathcal{R}(D^{*}) and R(D0)\mathcal{R}(D^{0})

    Full text link
    The ratios of branching fractions R(D)B(BˉDτνˉτ)/B(BˉDμνˉμ)\mathcal{R}(D^{*})\equiv\mathcal{B}(\bar{B}\to D^{*}\tau^{-}\bar{\nu}_{\tau})/\mathcal{B}(\bar{B}\to D^{*}\mu^{-}\bar{\nu}_{\mu}) and R(D0)B(BD0τνˉτ)/B(BD0μνˉμ)\mathcal{R}(D^{0})\equiv\mathcal{B}(B^{-}\to D^{0}\tau^{-}\bar{\nu}_{\tau})/\mathcal{B}(B^{-}\to D^{0}\mu^{-}\bar{\nu}_{\mu}) are measured, assuming isospin symmetry, using a sample of proton-proton collision data corresponding to 3.0 fb1{ }^{-1} of integrated luminosity recorded by the LHCb experiment during 2011 and 2012. The tau lepton is identified in the decay mode τμντνˉμ\tau^{-}\to\mu^{-}\nu_{\tau}\bar{\nu}_{\mu}. The measured values are R(D)=0.281±0.018±0.024\mathcal{R}(D^{*})=0.281\pm0.018\pm0.024 and R(D0)=0.441±0.060±0.066\mathcal{R}(D^{0})=0.441\pm0.060\pm0.066, where the first uncertainty is statistical and the second is systematic. The correlation between these measurements is ρ=0.43\rho=-0.43. Results are consistent with the current average of these quantities and are at a combined 1.9 standard deviations from the predictions based on lepton flavor universality in the Standard Model.Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2022-039.html (LHCb public pages

    Plant invaders in European and Mediterranean inland waters: profiles, distribution, and threats

    No full text
    The present brief and selective review focuses on a set of invasive alien aquatic plant species (notably the 21 listed by the European and Mediterranean Plant Protection Organisation, i.e., five A2 species, 11 invasive, 2 in the Observation List, 1 in the Alert List, 2 noteworthy), on definitions in use, on introduction pathways, and ecological effects, although the social and economic effects of freshwater invaders can be diverse and substantial. Legislation, literature, and scientific research dealing with plant invasions in inland waters often merge different types of invasive plant species and invaded habitats, as there are some overlappings between the concepts of macrophyte, aquatic plants, inland waters, wetlands, and riparian habitats. Freshwater ecosystems may well be the most endangered ecosystems in the world. Countless aquatic plants have been introduced in Europe and in the Mediterranean region, either deliberately because they were thought to be ornamental or otherwise desirable, or accidentally as releases from aquaria, dumping from water gardens, or contaminants. The escape of alien plants from managed environments is also frequent. Aquatic invaders have strong negative impacts on native biodiversity and many different impacts are reported in the literature for Europe and worldwide. Plant invasions in inland waters may be considered as one of a syndrome of factors that characterize degraded aquatic ecosystems. There are a number of risk analysis, impact assessment, ranking systems, decision trees, and prioritization methods available throughout Europe and the EPPO region, but the lack of a common framework for assessing the risks posed by invasive alien aquatic species is seen as a key gap. Successful management should include prevention, habitat restoration, dedicated risk assessment, prioritization, awareness raising, dedicated legislation, collaboration between different stakeholders, development of codes of conduct with the horticultural sector, and prohibiting the sale, purchase, and intentional release of some species in the wild. Actions to protect the European and Mediterranean inland waters from plants invasions are urgently needed and could provide overarching benefits

    The Exotic flora of Chad: a first contribution

    No full text
    A first inventory of the exotic flora of Chad has been compiled on the basis of the published literature, original distribution data collected by Global Positioning System field surveys (1999 to 2003), and plant exsiccata. A strictly geographical and conservative approach was adopted including only cultivated species and those with a native range separated from Chad territory. The reported aliens (131 taxa) represent approximately 6% of the total flora of the region (ca. 2,250 taxa). Most were introduced deliberately after 1823 (neophytes), from Central and tropical America. Agricultural weeds and ruderal species accounts for the 18%. Because source data may be underestimated, further assessments are proposed
    corecore