142 research outputs found

    Early development of rostrum saw-teeth in a fossil ray tests classical theories of the evolution of vertebrate dentitions

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    In classical theory, teeth of vertebrate dentitions evolved from co-option of external skin denticles into the oral cavity. This hypothesis predicts that ordered tooth arrangement and regulated replacement in the oral dentition were also derived from skin denticles. The fossil batoid ray Schizorhiza stromeri (Chondrichthyes; Cretaceous) provides a test of this theory. Schizorhiza preserves an extended cartilaginous rostrum with closely spaced, alternating saw-teeth, different from sawfish and sawsharks today. Multiple replacement teeth reveal unique new data from micro-CT scanning, showing how the 'cone-in-cone' series of ordered saw-teeth sets arrange themselves developmentally, to become enclosed by the roots of pre-existing saw-teeth. At the rostrum tip, newly developing saw-teeth are present, as mineralized crown tips within a vascular, cartilaginous furrow; these reorient via two 90° rotations then relocate laterally between previously formed roots. Saw-tooth replacement slows mid-rostrum where fewer saw-teeth are regenerated. These exceptional developmental data reveal regulated order for serial self-renewal, maintaining the saw edge with ever-increasing saw-tooth size. This mimics tooth replacement in chondrichthyans, but differs in the crown reorientation and their enclosure directly between roots of predecessor saw-teeth. Schizorhiza saw-tooth development is decoupled from the jaw teeth and their replacement, dependent on a dental lamina. This highly specialized rostral saw, derived from diversification of skin denticles, is distinct from the dentition and demonstrates the potential developmental plasticity of skin denticles

    Further Experimental Studies of Two-Body Radiative \Upsilon Decays

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    Continuing our studies of radiative Upsilon(1S) decays, we report on a search for Upsilon to gamma eta and Upsilon to gamma f_{J}(2220) in 61.3 pb^{-1} of e^{+}e^{-} data taken with the CLEO II detector at the Cornell Electron Storage Ring. For the gamma eta search the three decays of the eta meson to pi^{+}pi^{-}pi^{0}, pi^{0}pi^{0}pi^{0}, and gamma gamma were investigated. We found no candidate events in the two (3\pi)^{0} modes and no significant excess over expected backgrounds in the gamma gamma mode to set a limit on the branching fraction of B(Upsilon to gamma eta) < 2.1 x 10^{-5} at 90% C.L. The three charged two-body final states h h-bar (h = pi^{+}, K^{+}, p) were investigated for f_{J}(2220) production, with one, one, and two events found, respectively. Limits at 90% C.L. of B(\Upsilon to gamma f_{J}) x B(f_{J} to h h-bar) ~ 1.5 x 10^{-5} have been set for each of these modes. We compare our results to measurements of other radiative Upsilon decays, to measurements of radiative J/psi decays, and to theoretical predictions.Comment: 19 pages postscript, also available through http://w4.lns.cornell.edu/public/CLNS, submitted to Physical Review

    Update of the Search for the Neutrinoless Decay τμγ\tau\to \mu\gamma

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    We present an update of the search for the lepton family number violating decay τμγ\tau \to \mu\gamma using a complete CLEO II data sample of 12.6 million τ+τ\tau^+\tau^- pairs. No evidence of a signal has been found and the corresponding upper limit is \BR(\tau \to \mu\gamma) < 1.0 \times 10^{-6} at 90% CL, significantly smaller than previous limits. All quoted results are preliminary.Comment: 9 pages postscript, also available through http://w4.lns.cornell.edu/public/CLN

    Measurement of the Mass Splittings between the bbˉχb,J(1P)b\bar{b}\chi_{b,J}(1P) States

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    We present new measurements of photon energies and branching fractions for the radiative transitions: Upsilon(2S)->gamma+chi_b(J=0,1,2). The masses of the chi_b states are determined from the measured radiative photon energies. The ratio of mass splittings between the chi_b substates, r==(M[J=2]-M[J=1])/(M[J=1]-M[J=0]) with M the chi_b mass, provides information on the nature of the bbbar confining potential. We find r(1P)=0.54+/-0.02+/-0.02. This value is in conflict with the previous world average, but more consistent with the theoretical expectation that r(1P)<r(2P); i.e., that this mass splittings ratio is smaller for the chi_b(1P) triplet than for the chi_b(2P) triplet.Comment: 11 page postscript file, postscript file also available through http://w4.lns.cornell.edu/public/CLN

    Radiative Decay Modes of the D0D^{0} Meson

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    Using data recorded by the CLEO-II detector at CESR we have searched for four radiative decay modes of the D0D^0 meson: D0ϕγD^0\to\phi\gamma, D0ωγD^0\to\omega\gamma, D0KˉγD^0\to\bar{K}^{*}\gamma, and D0ρ0γD^0\to\rho^0\gamma. We obtain 90% CL upper limits on the branching ratios of these modes of 1.9×1041.9\times 10^{-4}, 2.4×1042.4\times 10^{-4}, 7.6×1047.6\times 10^{-4} and 2.4×1042.4\times 10^{-4} respectively.Comment: 15 page postscript file, postscript file also available through http://w4.lns.cornell.edu/public/CLN

    Search for Neutrinoless tau Decays Involving the K_S^0 Meson

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    We have searched for lepton flavor violating decays of the tau lepton with one or two KS0 mesons in the final state. The data used in the search were collected with the CLEO II and II.V detectors at the Cornell Electron Storage Ring (CESR) and correspond to an integrated luminosity of 13.9 fb^-1 at the Upsilon(4S) resonance. No evidence for signals were found, therefore we have set 90% confidence level (C.L.) upper limits on the branching fractions B(tau -> e KS0) mu KS0) e 2KS0) < 2.2e-6, and B(tau -> mu 2KS0) < 3.4e-6. These represent significantly improved upper limits on the two-body decays and first upper limits on the three-body decays.Comment: 9 pages postscript, also available through http://w4.lns.cornell.edu/public/CLNS, submitted to PRD Rapid Communication

    Studies of the Cabbibo-Suppressed Decays D+π0+νD^+ \to \pi^0 \ell^+ \nu and D+ηe+νeD^+ \to \eta e^+ \nu_e

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    Using 4.8 fb1^{-1} of data taken with the CLEO II detector, the branching fraction for the Cabibbo-suppressed decay D+π0+νD^+\to\pi^0\ell^+\nu measured relative to the Cabibbo favored decay D+K0ˉ+νD^+\to\bar{K^0}\ell^+\nu is found to be 0.046±0.014±0.0170.046\pm 0.014\pm 0.017. Using VcsV_{cs} and VcdV_{cd} from unitarity constraints, we determine f+π(0)/f+K(0)2=0.9±0.3±0.3| f_+^{\pi}(0)/f_+^K(0)|^2=0.9\pm 0.3\pm 0.3 We also present a 90% confidence level upper limit for the branching ratio of the decay D+ηe+νeD^+ \to \eta e^+\nu_e relative to that for D+π0e+νeD^+ \to \pi^0 e^+\nu_e of 1.5.Comment: 10 page postscript file, postscript file also available through http://w4.lns.cornell.edu/public/CLN

    New insights into the genetic etiology of Alzheimer's disease and related dementias

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    Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele
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