844 research outputs found

    Zoonotic potential of Giardia duodenalis and Cryptosporidium spp. and prevalence of intestinal parasites in young dogs from different populations on Prince Edward Island, Canada

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    The prevalence of Giardia duodenalis, Cryptosporidium spp. and other intestinal parasites was determined in dogs <1 year old from Prince Edward Island, Canada. Fecal samples were collected from the local animal shelter (n=62), private veterinary clinics (n=78) and a pet store (n=69). Intestinal parasites isolated included G. duodenalis, Cryptosporidium spp., Toxocara canis, Isospora spp. and Uncinaria stenocephala. To estimate the zoonotic risk associated with these infections, genotypes of G. duodenalis and Cryptosporidium spp. were determined using 16S rRNA and Hsp70 gene sequencing, respectively. Dogs from the pet store had the highest prevalence of intestinal parasites (78%, 95% CI: 68-88%), followed by the private veterinary clinics (49%, 95% CI: 37-60%), and the local animal shelter (34%, 95% CI: 22-46%). The majority G. duodenalis belonged to host-adapted assemblages D (47%, 95% CI: 31-64%) and C (26%, 95% CI: 13-43%), respectively. Zoonotic assemblages A and B were isolated alone or in mixed infections from 16% (95% CI: 6-31%) of G. duodenalis-positive dogs. All Cryptosporidium spp. were the host-adapted C. canis. While host-adapted, non-zoonotic G. duodenalis genotypes were more common, the presence of G. duodenalis assemblages A and B, T. canis, and U. stenocephala suggests that these dogs may present a zoonotic risk. The zoonotic risk from Cryptosporidium-infected dogs was minimal.Fabienne D. Uehlinger, Spencer J. Greenwood, J. Trenton McClure, Gary Conboy, Ryan O’Handley, Herman W. Barkem

    QUADRATIC HERMAN-WALLIS CORRECTION FACTORS FOR SYMMETRIC-TOP MOLECULES. APPLICATION TO THE H3+H_{3}^{+} ION.

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    1.^{1.} M. R. Aliev and J. K. G. Watson, in Molecular Spectroscopy: Modern Research, Vol. III (ed. K. Narahari Rao), pp. 1-67 (1985). 2.^{2.} S. Miller and J. Tennyson, Astrophys. J. 335, 486-490 (1988). 3.^{3.} W. A. Majewski, P. A. Feldman, J. K. G. Watson, S. Miller, and J. Tennyson, Astrophys. J. 347, L51-L54 (1989). 4.^{4.} W. A. Majewski, M. D. Marshall, A. R. W. McKellar, J. W. C. Johns, and J. K. G. Watson, J. Mol. Spectrosc, 122, 341-355 (1987). 5.^{5.} P. Drossart, J.-P. Maillard, J. Caldwell, S. J. Kim, J. K. G. Watson, W. A. Majewski, J. Tennyson, S. Miller, S. K. Atreya, J. T. Clarke, J. H. Waite, Jr., and R. Wagener, Nature 340, 539-541 (1989).Author Institution: Herzberg Institute of Astrophysics, National Research Council of Canada, OttawaThe Herman-Wallis correction factors to the intensities of allowed rovibronic transitions of symmetric-top molecules can be written in the form F={1+A1jmj+A1kmK+A2JJ(Q)[J(J+1)ms2+A2JJ(PR)mJ2+A2KKK2+A2JKmJMK}2F = \{1 + A_{1}^{j} mj + A_{1}^{k} m_{K} + A_{2}^{JJ(Q)}\sqrt{[J(J + 1)} - m_{s}^{2} + A_{2}^{JJ(PR)}m_{J}^{2} + A_{2}^{KK}\overline{K^{2}} + A_{2}^{JK} m_{J}M_{K}\}^{2} where mJ=12[J(J+1)J(J+1),mK=12[K2K2]J(J+1)=12J(J+1)+J(J+1)]m_{J} = \frac{1}{2} [J^{\prime}(J^{\prime} + 1) - J^{\prime\prime}(J^{\prime\prime} + 1), m_{K} = \frac{1}{2} [K^{2} - K^{\prime 2}]\overline{J(J + 1)} = \frac{1}{2} J^{\prime}(J^{\prime} + 1) + J^{\prime\prime}(J^{\prime\prime} + 1)], and K2=12[K2+(K2+K2]\overline{K^{2}} = \frac{1}{2}[K^{2}+ (K^{\prime 2} + K^{\prime 2}]. When different (J,K)(J,K)(J^{\prime},K^{\prime}) - (J^{\prime\prime},K^{\prime\prime}) transitions mix together, the square root of the above factor can be applied to each transition moment. For parallel bands the terms in mK are absent. In fundamental bands the A+2A_+{2} and A2A_{2} coefficients are related to the parameters ΘK7\Theta_{K}^{7} and Θkβ7\Theta_{k}^{\beta 7} in the effective dipole moment operator1operator^{1}. Values of the A1A_{1} and A2A_{2}, coefficients obtained by fitting the ab initio line strengths of H3+H_{3}^{+} calculated by Miller and Tennyson2,3Tennyson^{2,3} will be compared with the results of perturbation calculations. The correction factors are important at the high rotational temperatures observed in emission speetra in the laboratory3,4laboratory^{3,4} and from Jupiter5Jupiter^{5}

    EXPERIMENTAL DETERMINATION OF INFRARED TRANSITION DIPOLE MOMENTS FOR HNC FROM HERMAN-WALLIS EFFECT

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    g^{g}J. K. G. Watson, J. Mol. Spectrosc. 125, 428 (1987) h^{h}A. G. Maki et al. J. Mol. Spectrosc. 174, 365 (1995) i^{i}P. Botschwina et al, Chem. Phys. 190, 345 (1995) j^{j}T. J. Lee and A. P. Rendell, Chem. Phys. Lett. 177. 491 (1991)Author Institution: Institute for Astrophysics and Planetary Sciences, Ibaraki University; Institute for Astrophysics and Planetary Sciences, Nobeyama Radio ObservatoryThe transition dipole moments for the fundamental bands of HNC were obtained from analyses of Herman-Wallis effect on the absorption intensities. All the fundamental bands were measured using a Fourier transform infrared spectrometer (Bruker IFS 120HR) at Nobeyama Radio Observatory. A glow discharge in a mixture of CH3CNCH_{3}CN (50\sim 50 mTorr), H2(150  mTorr)H_{2}(\sim 150 \; mTorr), and Ar(100\sim 100 mTorr) was used for production of HNC The spectra were recorded with resolution of 0.01cm10.01 cm^{-1} and the absorption path length was 24 m. The experimentally determined first order Herman-Wallis coefficients for the ν1\nu_{1} and ν3\nu_{3} bands, combined with the relative value of the transition dipole moments for the ν1\nu_{1} and ν3\nu_{3} bands derived from the relative intensity measurements, yielded the following values for the transition dipole moments (in Debye), using the expressions for Herman-Wallis coefficients given by Watson8Watson^{8}. R1=0.194(13),R2=0.886(13),R3=0.169(11). R_{1} = 0.194(13),\quad R_{2} = -0.886 (13),\quad R_{3} = -0.169 (11). These values are considerably larger than the corresponding values for HCNhHCN^{h} and are in reasonable agreement with {ab initio} valuesijvalues^{ij}

    Mass capture and anesthesia of Australian bridled nailtail wallabies (Onychogalea fraenata) with the use of medetomidine and ketamine

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    We anesthetized 301 bridled nailtail wallabies (Onychogalea fraenata), captured within Scotia Sanctuary, New South Wales, Australia over four nights in October 2009 to perform health assessments before their release into a predator-proof exclosure. We tested two anesthetic dose-rate combinations, protocol 1 (0.08 mg/kg medetomidine-4.5 mg/kg ketamine), and protocol 2 (0.1 mg/kg medetomidine-5 mg/kg ketamine), each given intramuscularly. Median time from injection to recumbency for protocol 1 was 10 min (1-27 min) and for protocol 2 was 12 min (2-28) (P = 0.12). Five animals died during the induction with protocol 2; none died with protocol 1 (P = 0.06). Physiologic parameters were recorded during recumbency, with no significant abnormalities with protocol 1. Protocol 1 was an effective, efficient regime to anesthetize large numbers of bridled nailtail wallabies under field conditions.Wayne S. J. Boardman, Charles G. Caraguel, Sarah Gill, Kerryn Herman, Margaret-Mary McEwen, Leila C. Haghighi, and Ian Smit

    Divergent evolutionary processes associated with colonization of offshore islands

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    We dedicate this article to Michel Pascal, our outstanding co-author, who died on 5 January 2013, and to Anne Brundle, who gave us access to much archaeological material and who died in 2012. We acknowledge receipt of a Marie Curie Intra European Fellowship (to N.M.), support from the Swiss National Science Foundation (projects 31003A-127377, 3100A0-112072 and 3100-126074) to L.E. and G.H., funding from SYNTHESYS2 made available by the European Community Research Infrastructure under FP7 (‘Synthesis of Systematic Resources’, 226506-CP-CSA-Infra) to S.B., a Wellcome Trust University award to K.M.D. (GR071037) and overarching funding from the Arts and Humanities Research Council (project grant 119396). We thank V. Bretille, A. Frantz, M. Fuster, N. Gould, J. Herman, E. Jones, S. Martínek, R. Marwick, J. Michaux, S. Montuire, J. Pauperio, C. Scott, C. Tougard, B. Walther and N. Wheale for field specimens, T. White for assistance with IMa runs, and A. Ritchie, L. Shepherd and A. Sheridan for archaeological advice. We are grateful to the following for museum and archaeological samples: J. Barrett (MacDonald Institute, University of Cambridge), A. Brundle (Orkney Museum), C. David (Guernsey Museum), A. Ervynck (Flemish Heritage Institute), L. Gordon (Smithsonian Institute), J. Herman (National Museums of Scotland), D. Lee (Orkney College), R. Sabin (British Museum - Natural History, London) and G. Veron (Muséum national d'histoire naturelle, Paris).Peer reviewe

    ``ANOMALOUS'' RO-VIBRATIONAL INTENSITIES IN THE ΔV=1\Delta V = 1 BANDS OF SH(X2Π)SH(X^{2}\Pi)

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    1^{1} J.B. Burkholder, P.D. Hammer, C.J. Howard, A.G. Maki, G. Thompson, and C. Chackerian, Jr., J. Mol. Spectrosc. 124, 137 (1987). 2^{2} C. Chackerian, Jr., G. Guelachvili, A. Lopez-Pineiro. and R.H. Tipping, J. Chem. Phys. 90. 641 (1989). 3^{3} D.D. Nelson, Jr., A. Schiffman, D.J. Nesbitt and J.D. Yaron, J. Chem. Phys. (to be published).Author Institution: Laboratoire d'Infrarouge, Universite de Paris-Sud.; Laboratoire d'Infrarouge, NASA-Ames Research CenterRelative line Intensities of p- and r- branch transitions of diatomic radical molecules (ClO, NH, OH) have recently1-3 been used along with the theory of the Herman-Wallis effect to obtain estimates of electric dipole vibrational transition moments. Of the first and second row diatomic hydrides, ab initio calculations predict SH to exhibit the largest H.W. effect. Indeed, our spectra confirm a very large effect, and we present here an attempt at a quantitative analysis of the Herman-Wallis intensity perturbation in SH

    Fixation artifacts in rainbow-trout (Salmo-gairdner) gills - a morphometric evaluation

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    PT: J; CR: ALBASSAM M, 1987, VET PATHOL, V24, P34 BENVILLE PE, 1968, TOXICOL APPL PHARM, V12, P156 CHRETIEN M, 1986, BIOL CELL, V56, P137 DAOUST PY, 1984, VET PATHOL, V21, P93 DEJOUR P, 1981, PRINCIPLES COMP RESP ELLER LL, 1975, PATHOLOGY FISHES, P305 GRIZZLE JM, 1981, T AM FISH SOC, V110, P29 HARGENS AR, 1974, COMP BIOCH PHYSL A, V48, P675 HERMAN RL, 1985, T AM FISH SOC, V114, P911 HUGHES GM, 1979, WATER RES, V13, P665 LAURENT P, 1984, FISH PHYSIOL, V10, P73 MALLATT J, 1985, CAN J FISH AQUAT SCI, V42, P630 NICHOLS DJ, 1987, COMP BIOCHEM PHYS A, V87, P703 PERRY SF, 1984, FISH PHYSL B, V10, P324 RANDALL DJ, 1981, EVOLUTION AIRBREATHI RHODIN JAG, 1964, ANAT REC, V148, P420 ROBERTS RJ, 1978, FISH PATHOL, P55 ROBIN ED, 1973, NEW ENGL J MED, V238, P292 SNEDECOR GW, 1980, STATISTICAL METHODS THOMPSON SW, 1966, SELECTED HISTOCHEMIC WALSH AH, 1975, PATHOLOGY FISHES, P515 WEST JB, 1982, PULMONARY PATHOPHYSI WOBESER G, 1975, J FISH RES BOARD CAN, V32, P2005 ZENKER WGE, 1987, COMP BIOCHEM PHYS A, V86, P423; NR: 24; TC: 21; J9: CAN J FISHERIES AQUAT SCI; PG: 6; GA: U5947Source type: Electronic(1

    RESOLUTION OF A CONVERGENCE PROBLEM IN DIRECT-POTENTIAL-FIT DATA ANALYSES USING THE HERMAN-ASGHARIAN HAMILTONIAN

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    Author Institution: Department of Chemistry, University of Waterloo, Waterloo, Ontario; N2L 3G1, Canada; Department of Chemistry, Dalhousie University, Halifax, Nova Scotia,; B3H 4J3 Canada; Group de Spectrometrie Moleculaires et Atmospherique, CNRS UMR; 6089, BP 1039, F-51687, Reims Cedex 2, FranceThe effective radial Schrodinger equation based on the Herman-Asgharian}\, {\bf 19}, 305 (1966).} Hamiltonian for a diatomic molecule in a 1Σ^1\Sigma state has the form \vspace{-2mm} \begin{equation} -\,\frac{\hbar^2}{2\mu} [1 + \beta(r)] \frac{d^2\psi_{v,j}(r)}{dr^2 } + \left\{ \left[V_{\mathrm{CN}}(r) + \Delta V_{\mathrm{ad}}(r) \right] + \frac{ \hbar^2}{2\mu\,r^2} [1 + \alpha(r)] [J(J+1)] \right\} \psi_{v,j}(r) = E_{v,J} \psi_{v,j}(r) \label{eq:HAham} \end{equation} in which β(r)\,\beta(r)\, and α(r)\,\alpha(r)\, represent the effects of non-adiabatic corrections to the radial and angular kinetic energy operators, respectively, and ΔVad(r)\,\Delta V_{\mathrm{ad} }(r)\, is the adiabatic correction to the ``clamped nuclei'' potential energy function function VCN(r)\,V_{ \mathrm{CN}}(r)\,. An internal convergence problem encountered when utilizing wavefunction propagator methods for direct-potential-fit diatomic data analyses using this Hamiltonian is described and corrected. Improved Hamiltonian parameters for the ground states of GaH and ArH+^+ will be reported

    Reading acts of narrative appropriation: four instances of fraudulent memoir

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    PhDThis thesis examines acts of narrative appropriation, the telling of purportedly‘authentic’ life stories by those for whom the stories are not theirs to tell. This misuse or subversion of genre - the discipline of historical writing and the category of autobiography - becomes a means for cultural, social and political dissimulation, and the analysis focuses both on the act: the event, trespass, or ‘theft’ of another’s life story, and on the cultural meaning that this event reveals. These narrative acts are approached theoretically through discussions of what it means to be an author, a reader, and through the consideration of literary and social genre, category and form. In exploring identities at particular risk of appropriation, this thesis shows how fraudulent appropriated narratives affect our reading of the world, and in turn influence our perception of already marginalized social groups. My primary examples include prostitution ‘narratives’, Native North American ‘memoir,’ and fraudulent Holocaust survivor ‘testimony,’ with each text providing decoded evidence of ‘genre-bending’ exhibiting a social and political intent. These works seek to be read as authentic personal narratives, as autobiography, and that is how they have been presented to the reader. However, they are imposters – fictional tales desiring the elevated status of historical authenticity and willing to bend the rules and contracts of genre to achieve their end. Here the appearance of authenticity is achieved through the use of cultural and social ‘myth,’ or perceptions of cultural identity, and as such its fraudulent construction is first and foremost a social act, with a social and economic motivation. As this thesis concludes, these texts are most successful when their own political and social ideologies echo and confirm that of the readership; when their subjects, the fraudulent ‘I’ at the center of the text is also a performative elaboration of cultural belief
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