35 research outputs found

    Separating species and environmental determinants of leaf functional traits in temperate rainforest plants along a soil-development chronosequence

    Get PDF
    We measured a diverse range of foliar characteristics in shrub and tree species in temperate rainforest communities along a soil chronosequence (six sites from 8 to 120 000 years) and used multilevel model analysis to attribute the proportion of variance for each trait into genetic (G, here meaning species-level), environmental (E) and residual error components. We hypothesised that differences in leaf traits would be driven primarily by changes in soil nutrient availability during ecosystem progression and retrogression. Several leaf structural, chemical and gas-exchange traits were more strongly driven by G than E effects. For leaf mass per unit area (MA), foliar [N], net CO2 assimilation and dark respiration rates and foliar carbohydrate concentration, the G component accounted for 60–87% of the total variance, with the variability associated with plot, the E effect, much less important. Other traits, such as foliar [P] and N : P, displayed strong E and residual effects. Analyses revealed significant reductions in the slopes of G-only bivariate relationships when compared with raw relationships, indicating that a large proportion of trait–trait relationships is species based, and not a response to environment per se. This should be accounted for when assessing the mechanistic basis for using such relationships in order to make predictions of responses of plants to short-term environmental change

    Measurement of CP asymmetries and branching fraction ratios of B− decays to two charm mesons

    Get PDF
    The CPCP asymmetries of seven B−B^- decays to two charm mesons are measured using data corresponding to an integrated luminosity of 9fb−19\text{fb}^{-1} of proton-proton collisions collected by the LHCb experiment. Decays involving a D∗0D^{*0} or Ds∗−D^{*-}_s meson are analysed by reconstructing only the D0D^0 or Ds−D^-_s decay products. This paper presents the first measurement of ACP(B−→Ds∗−D0)\mathcal{A}^{CP}(B^- \rightarrow D^{*-}_s D^0) and ACP(B−→Ds−D∗0)\mathcal{A}^{CP}(B^- \rightarrow D^{-}_s D^{*0}), and the most precise measurement of the other five CPCP asymmetries. There is no evidence of CPCP violation in any of the analysed decays. Additionally, two ratios between branching fractions of selected decays are measured.The CP asymmetries of seven B−^{−} decays to two charm mesons are measured using data corresponding to an integrated luminosity of 9 fb−1^{−1} of proton-proton collisions collected by the LHCb experiment. Decays involving a D∗0^{*0} or Ds∗− {D}_s^{\ast -} meson are analysed by reconstructing only the D0^{0} or Ds− {D}_s^{-} decay products. This paper presents the first measurement of ACP \mathcal{A} ^{CP}(B−^{−}→Ds∗− {D}_s^{\ast -} D0^{0}) and ACP \mathcal{A} ^{CP}(B−^{−}→Ds− {D}_s^{-} D∗0^{∗0}), and the most precise measurement of the other five CP asymmetries. There is no evidence of CP violation in any of the analysed decays. Additionally, two ratios between branching fractions of selected decays are measured.[graphic not available: see fulltext]The CPCP asymmetries of seven B−B^- decays to two charm mesons are measured using data corresponding to an integrated luminosity of 9 fb−19\text{ fb}^{-1} of proton-proton collisions collected by the LHCb experiment. Decays involving a D∗0D^{*0} or Ds∗−D^{*-}_s meson are analysed by reconstructing only the D0D^0 or Ds−D^-_s decay products. This paper presents the first measurement of ACP(B−→Ds∗−D0)\mathcal{A}^{CP}(B^- \rightarrow D^{*-}_s D^0) and ACP(B−→Ds−D∗0)\mathcal{A}^{CP}(B^- \rightarrow D^{-}_s D^{*0}), and the most precise measurement of the other five CPCP asymmetries. There is no evidence of CPCP violation in any of the analysed decays. Additionally, two ratios between branching fractions of selected decays are measured

    Two Unique Human Decidual Macrophage Populations

    No full text

    Cryopreservation of Hydractinia symbiolongicarpus Sperm to Support Community-Based Repository Development for Preservation of Genetic Resources

    No full text
    Hydractinia symbiolongicarpus is an emerging model organism in which cutting-edge genomic tools and resources are being developed for use in a growing number of research fields. One limitation of this model system is the lack of long-term storage for genetic resources. The goal of this study was to establish a generalizable cryopreservation approach for Hydractinia that would support future repository development for other cnidarian species. Specific objectives were to: (1) characterize basic parameters related to sperm quality; (2) develop a generalizable approach for sperm collection; (3) assess the feasibility of in vitro fertilization (IVF) with sperm after refrigerated storage; (4) assess the feasibility of IVF with sperm cryopreserved with various sperm concentrations; (5) evaluate feasibility of cryopreservation with various freezing conditions, and (6) explore the feasibility of cryopreservation by use of a 3-D printed open-hardware (CryoKit) device. Animal husbandry and sperm collection were facilitated by use of 3-D printed open hardware. Hydractinia sperm at a concentration of 2 × 107 cells/mL stored at 4 °C for 6 d were able to achieve 50% fertilization rate. It appeared that relatively higher sperm concentration (>5 × 107 cells/mL) for cryopreservation could promote fertilization. A fertilization rate of 41–69% was observed using sperm equilibrated with 5, 10, or 15% (v/v) cryoprotectant (dimethyl sulfoxide or methanol) for 20 min, cooled at a rate of 5, 10, or 20 °C/min from 4 °C to −80 °C, at a cell concentration of 108/mL, in 0.25 mL French straws. Samples cryopreserved with the CryoKit produced a fertilization rate of 72–82%. Establishing repository capabilities for the Hydractinia research community will be essential for future development, maintenance, protection, and distribution of genetic resources. More broadly, these generalizable approaches can be used as a model to develop germplasm repositories for other cnidarian species

    Differential Effect of Allorecognition Loci on Phenotype in Hydractinia symbiolongicarpus (Cnidaria: Hydrozoa)

    No full text
    The allorecognition complex of Hydractinia symbiolongicarpus is a chromosomal interval containing two loci, alr1 and alr2, that controls fusion between genetically distinct colonies. Recombination between these two loci has been associated with a heterogeneous class of phenotypes called transitory fusion. A large-scale backcross was performed to generate a population of colonies (N = 106) with recombination breakpoints within the allorecognition complex. Two distinct forms of transitory fusion were correlated with reciprocal recombination products, suggesting that alr1 and alr2 contributed differentially to the allorecognition response. Specifically, type I transitory fusion is associated with rapid and persistent separation of allogeneic tissues, whereas type II transitory fusion generates a patchwork of continuously fusing and separating tissues

    Cnidofest 2022: hot topics in cnidarian research

    Get PDF
    Abstract The second annual Cnidarian Model Systems Meeting, aka “Cnidofest”, took place in Davis, California from 7 to 10th of September, 2022. The meeting brought together scientists using cnidarians to study molecular and cellular biology, development and regeneration, evo-devo, neurobiology, symbiosis, physiology, and comparative genomics. The diversity of topics and species represented in presentations highlighted the importance and versatility of cnidarians in addressing a wide variety of biological questions. In keeping with the spirit of the first meeting (and its predecessor, Hydroidfest), almost 75% of oral presentations were given by early career researchers (i.e., graduate students and postdocs). In this review, we present research highlights from the meeting
    corecore