Avaliação de populações de planorbídeos, em habitats naturais, pelo método de perfuração da concha

Propõe-se um novo método de marcação de planorbídeos para determinação de densidade e de outros parâmetros pertinentes ao estudo de dinâmica de população, como capacidade de migração, taxas de crescimento e potencial biótico nos habitats naturais. Consiste em marcação através de dois furos de cerca de 2 mm de diâmetro de cada lado da concha em sua extremidade anterior, usando-se um estilete metálico. Após a marcação os caramujos são imediatamente reintroduzidos no habitat, em local correspondente ao da captura processada poucos minutos antes. Nos experimentos realizados, as taxas de caramujos marcados, recapturados uma semana após a marcação, variaram de 14 a 18% e permitiram calcular a população total de B. glabrata, de 5 mm de diâmetro ou mais. O método permite estimar também a população de jovens com menos de 5 mm e fazer marcações múltiplas. É muito simples, de fácil manejo, não exige equipamentos nem pessoal especializados e provoca menos impacto no ambiente do que outros métodos

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

Jet fragmentation functions are measured for the first time in proton-proton collisions for charged pions, kaons, and protons within jets recoiling against a $Z$ boson. The charged-hadron distributions are studied longitudinally and transversely to the jet direction for jets with transverse momentum 20 $< p_{\textrm{T}} < 100$ GeV and in the pseudorapidity range $2.5 < \eta < 4$. 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 fb$^{-1}$. 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 B−→Λc+Λˉc−K−B^{-} \to \Lambda_{c}^{+} \bar{\Lambda}_{c}^{-} K^{-} decay

The decay $B^{-} \to \Lambda_{c}^{+} \bar{\Lambda}_{c}^{-} K^{-}$ is studied in proton-proton collisions at a center-of-mass energy of $\sqrt{s}=13$ TeV using data corresponding to an integrated luminosity of 5 $\mathrm{fb}^{-1}$ collected by the LHCb experiment. In the $\Lambda_{c}^+ K^{-}$ system, the $\Xi_{c}(2930)^{0}$ state observed at the BaBar and Belle experiments is resolved into two narrower states, $\Xi_{c}(2923)^{0}$ and $\Xi_{c}(2939)^{0}$, whose masses and widths are measured to be $$m(\Xi_{c}(2923)^{0}) = 2924.5 \pm 0.4 \pm 1.1 \,\mathrm{MeV}, \\ m(\Xi_{c}(2939)^{0}) = 2938.5 \pm 0.9 \pm 2.3 \,\mathrm{MeV}, \\ \Gamma(\Xi_{c}(2923)^{0}) = \phantom{000}4.8 \pm 0.9 \pm 1.5 \,\mathrm{MeV},\\ \Gamma(\Xi_{c}(2939)^{0}) = \phantom{00}11.0 \pm 1.9 \pm 7.5 \,\mathrm{MeV},$$ where the first uncertainties are statistical and the second systematic. The results are consistent with a previous LHCb measurement using a prompt $\Lambda_{c}^{+} K^{-}$ sample. Evidence of a new $\Xi_{c}(2880)^{0}$ state is found with a local significance of $3.8\,\sigma$, whose mass and width are measured to be $2881.8 \pm 3.1 \pm 8.5\,\mathrm{MeV}$ and $12.4 \pm 5.3 \pm 5.8 \,\mathrm{MeV}$, respectively. In addition, evidence of a new decay mode $\Xi_{c}(2790)^{0} \to \Lambda_{c}^{+} K^{-}$ is found with a significance of $3.7\,\sigma$. The relative branching fraction of $B^{-} \to \Lambda_{c}^{+} \bar{\Lambda}_{c}^{-} K^{-}$ with respect to the $B^{-} \to D^{+} D^{-} K^{-}$ decay is measured to be $2.36 \pm 0.11 \pm 0.22 \pm 0.25$, 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})

The ratios of branching fractions $\mathcal{R}(D^{*})\equiv\mathcal{B}(\bar{B}\to D^{*}\tau^{-}\bar{\nu}_{\tau})/\mathcal{B}(\bar{B}\to D^{*}\mu^{-}\bar{\nu}_{\mu})$ and $\mathcal{R}(D^{0})\equiv\mathcal{B}(B^{-}\to D^{0}\tau^{-}\bar{\nu}_{\tau})/\mathcal{B}(B^{-}\to D^{0}\mu^{-}\bar{\nu}_{\mu})$ are measured, assuming isospin symmetry, using a sample of proton-proton collision data corresponding to 3.0 fb${ }^{-1}$ of integrated luminosity recorded by the LHCb experiment during 2011 and 2012. The tau lepton is identified in the decay mode $\tau^{-}\to\mu^{-}\nu_{\tau}\bar{\nu}_{\mu}$. The measured values are $\mathcal{R}(D^{*})=0.281\pm0.018\pm0.024$ and $\mathcal{R}(D^{0})=0.441\pm0.060\pm0.066$, where the first uncertainty is statistical and the second is systematic. The correlation between these measurements is $\rho=-0.43$. 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

Schistosoma mansoni: avaliação da atividade da oxamniquina (Mansil*) em esquistossômulos com 24 horas após infecção

Mice transcutaneously infected with about 400 cercariae were submitted to treatment with oxamniquine (400 mg/kg), 24 hours after infection. The recovery of schistosomules, at 4, 24, 48 and 72 hours and 35 days after treatment, showed the activity of the drug on the parasites, thus practically preventing their migration from the skin to the lungs. Worm recovery performed in the lungs (96 hours after treatment) showed recovery means of 0.6 worms/mouse in the treated group and 53.8 in the control group (untreated). The perfusion of the portal system carried out at 35 days after treatment clearly showed the elimination of all the parasites in the treated group, whereas a recovery mean of 144.7 worms/mouse was detected in the control group (untreated). These findings confirm the efficacy of oxamniquine at the skin phase of infection, and also show similarity with the immunization method that uses irradiated cercariae. The practical application of these findings in the medical clinic is discussed tooCamundongos infectados transcutaneamente com cerca de 400 cercárias foram submetidos a tratamento com oxamniquina (400 mg/kg), 24 horas após a infecção. A recuperação dos esquistossômulos a nível da pele mostrou a atividade da droga nos parasitos e impediu praticamente sua migração para os pulmões. A recuperação a nível pulmonar (96 horas após tratamento) mostrou uma média de 0,6 vermes por camundongo no grupo tratado e 53,8 no grupo controle, não tratado. A perfusão do sistema porta, realizada aos 35 dias após infecção, mostrou claramente a eliminação de todos os parasitos no grupo tratado, enquanto foi recuperada uma média de 144,7 vermes no grupo controle, não tratado. Estes achados vem comprovar a eficácia da oxamniquina na fase cutânea da infecção e mostra analogia com o sistema de imunização que usa cercárias irradiadas. Também se discute a aplicação destes resultados na clínic

Avaliação de populações de planorbídeos, em habitats naturais, pelo método de perfuração da concha

A new method for labeling planorbidae to estimate the density and other parameters related with population studies, such as migration capacity, growth rates and biotic potential in natural habitats, is proposed. The snails are labelled with two small holes (2 mm diameter each) perforated in each side of the shell by means of a pointed metalic tool. After labeling, the snails are immediately put back in their habitat, at the same site where they were captured a few minutes ago. In all experiments carried out, the rates of labelled snails, recovered a week after labeling, varied from 14 to 18% and allowed to estimate the total population of B. glabrata, with 5 mm diameter or more. This method enables to evaluate juvenile population (with less than 5 mm), as well as to perform different marks. It is very simple/ease of handling; it does not require either specialized personnel or equipment and, on the other hand, it causes less trouble in the habitat than other procedures do.Propõe-se um novo método de marcação de planorbídeos para determinação de densidade e de outros parâmetros pertinentes ao estudo de dinâmica de população, como capacidade de migração, taxas de crescimento e potencial biótico nos habitats naturais. Consiste em marcação através de dois furos de cerca de 2 mm de diâmetro de cada lado da concha em sua extremidade anterior, usando-se um estilete metálico. Após a marcação os caramujos são imediatamente reintroduzidos no habitat, em local correspondente ao da captura processada poucos minutos antes. Nos experimentos realizados, as taxas de caramujos marcados, recapturados uma semana após a marcação, variaram de 14 a 18% e permitiram calcular a população total de B. glabrata, de 5 mm de diâmetro ou mais. O método permite estimar também a população de jovens com menos de 5 mm e fazer marcações múltiplas. É muito simples, de fácil manejo, não exige equipamentos nem pessoal especializados e provoca menos impacto no ambiente do que outros métodos

Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types

Summary: Hotspot mutations in splicing factor genes have been recently reported at high frequency in hematological malignancies, suggesting the importance of RNA splicing in cancer. We analyzed whole-exome sequencing data across 33 tumor types in The Cancer Genome Atlas (TCGA), and we identified 119 splicing factor genes with significant non-silent mutation patterns, including mutation over-representation, recurrent loss of function (tumor suppressor-like), or hotspot mutation profile (oncogene-like). Furthermore, RNA sequencing analysis revealed altered splicing events associated with selected splicing factor mutations. In addition, we were able to identify common gene pathway profiles associated with the presence of these mutations. Our analysis suggests that somatic alteration of genes involved in the RNA-splicing process is common in cancer and may represent an underappreciated hallmark of tumorigenesis. : Seiler et al. report that 119 splicing factor genes carry putative driver mutations over 33 tumor types in TCGA. The most common mutations appear to be mutually exclusive and are associated with lineage-independent altered splicing. Samples with these mutations show deregulation of cell-autonomous pathways and immune infiltration. Keywords: splicing, SF3B1, U2AF1, SRSF2, RBM10, FUBP1, cancer, mutatio