Showing 4911 - 4920 of 5831 Items
Bowdoin College Catalogue (1946-1947)
Date: 1947-01-01
Access: Open access
- Bowdoin College Bulletin no. 284
Bowdoin College Catalogue (1954-1955)
Date: 1955-01-01
Access: Open access
- Bowdoin College Bulletin no. 314
Measurements of semileptonic branching fractions of B mesons at the '(4S) resonance
Date: 1992-01-01
Creator: S. Henderson, K. Kinoshita, F. Pipkin, M. Procario, M., Saulnier, R. Wilson, J. Wolinski, D. Xiao, R. Ammar, P. Baringer, D. Coppage, R. Davis, P. Haas, M. Kelly, N. Kwak, Ha Lam, S. Ro, Y. Kubota, J. K. Nelson, D. Perticone, R. Poling, S. Schrenk, G. Crawford, R. Fulton, T. Jensen, D. R. Johnson, H. Kagan, R. Kass, R. Malchow, F. Morrow, J. Whitmore
Access: Open access
- We report new measurements of semileptonic branching fractions of B mesons produced at the '(4S) resonance determined by fitting the inclusive electron and muon momentum spectra to different theoretical models. Using B(B»'X"-») to denote the average of the semileptonic branching fractions for B decay to electrons and muons, we obtain B(B»'X"-»)= (10.5±0.2±0.4)% using the refined free-quark model of Altarelli et al., and B(B»'X"-»)=(11.2±0.3±0.4)% using a modified version of the form-factor model of Isgur et al., in which the D**"-» contribution is allowed to float in the fit. The average of these two results is B(B»'X"-»)=(10.8±0. 2±0.4±0.4)%, where the errors are statistical, systematic uncertainties in the measurement, and systematic uncertainties associated with the theoretical models, respectively. Semileptonic branching fractions as low as this are difficult to accommodate in theoretical models where hadronic B-meson decays arise only from spectator diagrams. We use dilepton yields to limit the uncertainty in the semileptonic branching fraction due to the possible existence of non-BB» decays of the '(4S). In addition, we tag neutral B mesons using the decays B»0'D*+- and B»0'D*+"-» to obtain the first direct measurement of semileptonic branching fractions for neutral B mesons; the average of the electron and muon results for neutral B mesons is B(B»0'X"-»)=(9.9±3.0±0.9)%. © 1992 The American Physical Society.
SIFamide peptides modulate cardiac activity differently in two species of Cancer crab
Date: 2019-10-01
Creator: Patsy S. Dickinson, Heidi M. Samuel, Elizabeth A. Stemmler, Andrew E. Christie
Access: Open access
- The SIFamides are a broadly conserved arthropod peptide family characterized by the C-terminal motif –SIFamide. In decapod crustaceans, two isoforms of SIFamide are known, GYRKPPFNGSIFamide (Gly1-SIFamide), which is nearly ubiquitously conserved in the order, and VYRKPPFNGSIFamide (Val1-SIFamide), known only from members of the astacidean genus Homarus. While much work has focused on the identification of SIFamide isoforms in decapods, there are few direct demonstrations of physiological function for members of the peptide family in this taxon. Here, we assessed the effects of Gly1- and Val1-SIFamide on the cardiac neuromuscular system of two closely related species of Cancer crab, Cancer borealis and Cancer irroratus. In each species, both peptides were cardioactive, with identical, dose-dependent effects elicited by both isoforms in a given species. Threshold concentrations for bioactivity are in the range typically associated with hormonal delivery, i.e., 10−9 to 10−8 M. Interestingly, and quite surprisingly, while the predicted effects of SIFamide on cardiac output are similar in both C. borealis and C. irroratus, frequency effects predominate in C. borealis, while amplitude effects predominate in C. irroratus. These findings suggest that, while SIFamide is likely to increase cardiac output in both crabs, the mechanism through which this is achieved is different in the two species. Immunohistochemical/mass spectrometric data suggest that SIFamide is delivered to the heart hormonally rather than locally, with the source of hormonal release being midgut epithelial endocrine cells in both Cancer species. If so, midgut-derived SIFamide may function as a regulator of cardiac output during the process of digestion.
Statement by Douglas Chapman collected by Erika Bjorum on August 9, 2023
Date: 2023-08-09
Creator: Douglas Chapman
Access: Open access
- This statement was given privately.
Measurement of baryon production in B-meson decay
Date: 1992-01-01
Creator: G. Crawford, R. Fulton, T. Jensen, D. R. Johnson, H., Kagan, R. Kass, R. Malchow, F. Morrow, J. Whitmore, P. Wilson, D. Bortoletto, D. Brown, J. Dominick, R. L. McIlwain, D. H. Miller, M. Modesitt, C. R. Ng, S. F. Schaffner, E. I. Shibata, I. P.J. Shipsey, M. Battle, H. Kroha, K. Sparks, E. H. Thorndike, C. H. Wang, M. S. Alam, I. J. Kim, W. C. Li, X. C. Lou, B. Nemati, V. Romero
Access: Open access
- Using the CLEO detector at the Cornell Electron Storage Ring, we observe B-meson decays to c+ and report on improved measurements of inclusive branching fractions and momentum spectra of other baryons. For the inclusive decay Bc+X with c+pK-+, we find that the product branching fraction B(Bc+X)B(c+pK-+)=(0.273±0.051±0.039)%. Our measured inclusive branching fractions to noncharmed baryons are B(BpX)=(8.0±0.5±0.3)%, B(BX)=(3.8±0.4±0.6)%, and B(B-X)=(0.27±0.05±0.04)%. From these rates and studies of baryon-lepton and baryon-antibaryon correlations in B decays, we have estimated the branching fraction B(Bc+X) to be (6.40.8±0.8)%. Combining these results, we calculate B(c+pK-) to be (4.3±1.0±0.8)%. © 1992 The American Physical Society.
Ds+ decays to + and +
Date: 1992-01-01
Creator: J. Alexander, C. Bebek, K. Berkelman, D. Besson, T. E., Browder, D. G. Cassel, E. Cheu, D. M. Coffman, P. S. Drell, R. Ehrlich, R. S. Galik, M. Garcia-Sciveres, B. Geiser, B. Gittelman, S. W. Gray, D. L. Hartill, B. K. Heltsley, K. Honscheid, J. Kandaswamy, N. Katayama, P. C. Kim, D. L. Kreinick, J. D. Lewis, G. S. Ludwig, J. Masui, J. Mevissen, N. B. Mistry, S. Nandi, C. R. Ng, E. Nordberg, C. Grady
Access: Open access
- Using the CLEO II detector, we have accurately measured Ds decay branching ratios relative to the mode for the and states, for which there are conflicting claims; our results are 0.540.090.06 and 1.200.150.11, respectively. © 1992 The American Physical Society.
Bowdoin College Catalogue (1940-1941)
Date: 1941-01-01
Access: Open access
- Bowdoin College Bulletin no. 255
Chambers of Reflection: Rousseau, Tocqueville, and Self-Government in the Digital Age
Date: 2020-01-01
Creator: John Sweeney
Access: Open access
- Jean-Jacques Rousseau and Alexis de Tocqueville each warn that the dominant cultures of their days may hinder the project of self-government. Against the backdrop of advancing Enlightenment philosophy, Rousseau writes that as social visibility increases relative to intimate connection, the drive for recognition corrupts self-love. Following the American and French revolutions, Tocqueville explores the democratic erosion of social hierarchies. He writes that a rise in individualism may obscure “self-interest well-understood”—the perspective gained through collaboration with others, thoughtful reflection, and reverence for truths that lie beyond the dictates of cursory instincts. In this project, I apply these political theories to the Digital Age. I explain how the distinction between the physical world and the digital realm has actualized Rousseau’s depiction of double men, “always appearing to relate everything to others and never relating anything except to themselves alone.” In the era of social distancing, technological evolution threatens to induce regression in the sociability and reflective agency that promote our capacity for self-government. Accordingly, I argue that Rousseau’s theory of corrupted drive for recognition and Tocqueville’s theory of individualism inform a new danger to political freedom: digital tribalism.
Multiple transcriptome mining coupled with tissue specific molecular cloning and mass spectrometry provide insights into agatoxin-like peptide conservation in decapod crustaceans
Date: 2020-12-01
Creator: Andrew E. Christie, Cindy D. Rivera, Catherine M. Call, Patsy S. Dickinson, Elizabeth A., Stemmler, J. Joe Hull
Access: Open access
- Over the past decade, in silico genome and transcriptome mining has led to the identification of many new crustacean peptide families, including the agatoxin-like peptides (ALPs), a group named for their structural similarity to agatoxin, a spider venom component. Here, analysis of publicly accessible transcriptomes was used to expand our understanding of crustacean ALPs. Specifically, transcriptome mining was used to investigate the phylogenetic/structural conservation, tissue localization, and putative functions of ALPs in decapod species. Transcripts encoding putative ALP precursors were identified from one or more members of the Penaeoidea (penaeid shrimp), Sergestoidea (sergestid shrimps), Caridea (caridean shrimp), Astacidea (clawed lobsters and freshwater crayfish), Achelata (spiny/slipper lobsters), and Brachyura (true crabs), suggesting a broad, and perhaps ubiquitous, conservation of ALPs in decapods. Comparison of the predicted mature structures of decapod ALPs revealed high levels of amino acid conservation, including eight identically conserved cysteine residues that presumably allow for the formation of four identically positioned disulfide bridges. All decapod ALPs are predicted to have amidated carboxyl-terminals. Two isoforms of ALP appear to be present in most decapod species, one 44 amino acids long and the other 42 amino acids in length, both likely generated by alternative splicing of a single gene. In carideans, a gene or terminal exon duplication appears to have occurred, with alternative splicing producing four ALPs, two 44 and two 42 amino acid isoforms. The identification of ALP precursor-encoding transcripts in nervous system-specific transcriptomes (e.g., Homarus americanus brain, eyestalk ganglia, and cardiac ganglion assemblies, finding confirmed using RT-PCR) suggests that members of this peptide family may serve as locally-released and/or hormonally-delivered neuromodulators in decapods. Their detection in testis- and hepatopancreas-specific transcriptomes suggests that members of the ALP family may also play roles in male reproduction and innate immunity/detoxification.