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Psittacine Birds (psittacine + bird)
Selected AbstractsCharacterization of Pasteurellaceae-like bacteria isolated from clinically affected psittacine birdsJOURNAL OF APPLIED MICROBIOLOGY, Issue 4 2010R.H. Gregersen Abstract Aims:, The aim of the present investigation was to identify and characterize Pasteurella -like isolates obtained from clinically affected psittacine birds. Methods and Results:, A total of 37 isolates from psittacine birds tentatively classified with the family Pasteurellaceae were characterized phenotypically. The genetic relationship was investigated by sequencing of partial rpoB and 16S rRNA genes for selected isolates. The results obtained were compared with the data from 16 reference strains. Nine isolates were identified as Gallibacterium spp., 16 as Volucribacter spp. or Volucribacter- like, while 11 isolates were classified as taxon 44 of Bisgaard. A single isolate was identified as Pasteurella multocida. Conclusions:, Characterization of Pasteurellaceae by traditional methods is often inconclusive because of inconsistent reactions and phenotypic diversity. For the same reason, genotyping is essential to allow proper classification as demonstrated in the present study. Significance and Impact of the Study:, Limited information exists on the isolation and significance of Pasteurellaceae associated with clinically affected psittacine birds showing signs of digestive and/or respiratory disorders. The present investigations demonstrated that these organisms are widely distributed among clinically affected birds, but isolation of these taxa cannot be unambiguously correlated with the symptoms observed. [source] Eucalyptus pollen grain emptying by two Australian nectarivorous psittacinesJOURNAL OF AVIAN BIOLOGY, Issue 3 2001B. D. Gartrell The relative importance of pollen as a source of protein to vertebrates is controversial. In nectarivorous psittacine birds, field studies support its importance, but an experimental study in a nectarivorous parrot showed that less than 7% of pollen grains were emptied. We investigated pollen grain emptying by two nectarivorous Australian parrots, the Swift Parrot Lathamus discolor and the Musk Lorikeet Glossopsitta concinna. We used a controlled experiment, and examined pollen located at different levels through the alimentary tract of wild L. discolor. There was significant emptying of pollen grains (x=45.4%±1.91 s.e.) by all birds in the experimental trials. There was also a progressive increase in the percentage of pollen grains emptied at different sites along the alimentary tract in wild birds (crop x=24.2%±4.44 s.e., proventriculus x=34.0%±7.29 s.e., duodenum x=54.3%±5.42 s.e. and distal intestine x=64.2%±4.68 s.e.). The percentage of pollen grains emptied by captive L. discolor in the experimental trial (x=44.1%±2.77 s.e.) was not significantly different from that found in wild L. discolor (x=40.3%±4.25 s.e.). Both species of nectarivorous parrot were able to rapidly ingest large quantities of Eucalyptus pollen and appeared to empty the pollen grains efficiently. Eucalyptus pollen appears to be an important source of protein for these birds. [source] Investigation of Japanese quail (Coturnix japonica) as a pharmacokinetic model for cockatiels (Nymphicus hollandicus) and Poicephalus parrots via comparison of the pharmacokinetics of a single intravenous injection of oxytetracycline hydrochlorideJOURNAL OF VETERINARY PHARMACOLOGY & THERAPEUTICS, Issue 6 2005A. OSOFSKY The purpose of this study was to determine whether Japanese quail (Coturnix japonica) would serve as a pharmacokinetic animal model for two small companion parrots: cockatiels (Nymphicus hollandicus) and Poicephalus parrots. Oxytetracycline (OTC) was the pharmacologic agent chosen for this study as it is eliminated primarily by renal glomerular filtration and undergoes minimal metabolism. A single intravenous injection of 20 mg/kg oxytetracycline hydrochloride was administered to the three study groups and blood samples were obtained at 5, 10, 15, and 30 min post-OTC injection as well as 1, 2, 4, 8, 12 and 24 h post-OTC injection. Quantification of plasma OTC was accomplished using a standardized microbial inhibition assay. Naïve-pooled data (NPD) analysis of the plasma concentration,time profile of OTC best fit a two-compartment open model for all three avian species. Noncompartmental analysis of the mean data yielded the following parameters for quail, cockatiels and Poicephalus parrots respectively: ,z = 3.14, 4.57, 3.71 h; AUC = 38.9, 42.7, 49.6 ,g·h/mL; and Cl = 514, 468, 403 mL/h/kg. Based on the similarity of these pharmacokinetic parameters, it appears that quail could be used as a model species to predict the appropriate OTC dosing regimen for small psittacine birds. A bootstrap procedure was also applied to these sparse data sets for both compartmental and noncompartmental analysis. The bootstrap procedure allowed for the calculation of variability of parameters; however, the estimates of the parameters were very similar to those calculated using the NPD and the data mean values. [source] The evolution of learningBIOLOGICAL REVIEWS, Issue 2 2004Bruce R. Moore ABSTRACT Most processes or forms of learning have been treated almost as special creations, each as an independent process unrelated to others. This review offers an evolutionary cladogram linking nearly one hundred forms of learning and showing the paths through which they evolved. Many processes have multiple forms. There are at least five imprinting processes, eleven varieties of Pavlovian conditioning, ten of instrumental conditioning, and eight forms of mimicry and imitation. Song learning evolved independently in at least six groups of animals, and movement imitation in three (great apes, cetaceans and psittacine birds). The cladogram also involves at least eight new processes: abstract concept formation, percussive mimicry, cross-modal imitation, apo-conditioning, hybrid conditioning, proto-pantomime, prosodic mimicry, and image-mediated learning. At least eight of the processes evolved from more than one source. Multiple sources are of course consistent with modern evolutionary theory, as seen in some obligate symbionts, and gene-swapping organisms. Song learning is believed to have evolved from two processes: auditory imprinting and skill learning. Many single words evolved from three sources: vocal mimicry, discrimination learning, and abstract concept formation. [source] | ||||||||||