4,051 research outputs found

    Solvent Deactivation of Mimosa Webworm Larval Webbing (Lepidoptera: Plutellidae)

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    Untreated larval webbing of the mimosa webworm, Homadaula anisocentra stimulated oviposition. Six-week-old webbing was as active as two-day-old webbing. Stimulatory activity of webbing was lost after rinsing with highly polar solvents, but not after rinsing with nonpolar solvents. Addition of the polar solvent rinses did not induce activity in other substrates nor restore activity to rinsed webbing. No differences in structure were found in a scanning electron microscope examination of unrinsed webbing and webbing rinsed with solvents of varying polarity

    Oviposition Preference of the Mimosa Webworm, Homadaula anisocentra (Lepidoptera: Plutellidae)

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    In the field, the mimosa webworm, Homadaula anisocentra Meyrick (Lepidoptera: Plutellidae), oviposits preferentially on branches or on leaf rachises or petioles of uninfested ornamental honeylocust, Gleditsia triacanthos L. On infested trees, oviposition occurs almost entirely on larval webbing. In the laboratory, uninfested mature leaves of both honeylocust and mimosa, Albizzia julibrissin Durazzini, are preferred over uninfested young leaves as oviposition sites. The addition of larval webbing to leaves of any age or to nonhost substrate induces oviposition preferentially on the webbin

    Pressure Measurement in Supersonic Air Flow by Differential Absorptive Laser-Induced Thermal Acoustics

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    Nonintrusive, off-body flow barometry in Mach-2 airflow has been demonstrated in a large-scale supersonic wind tunnel using seedless laser-induced thermal acoustics (LITA). The static pressure of the gas flow is determined with a novel differential absorption measurement of the ultrasonic sound produced by the LITA pump process. Simultaneously, stream-wise velocity and static gas temperature of the same spatially-resolved sample volume were measured with this nonresonant time-averaged LITA technique. Mach number, temperature and pressure have 0.2%, 0.4%, and 4% rms agreement, respectively, in comparison with known free-stream conditions

    Effects of Cardiac Structural Remodelling During Heart Failure on Cardiac Excitation – Insights from a Heterogeneous 3D Model of the Rabbit Atria

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    Heart failure is a leading cause of morbidity and mortality in the western world. One of the effects of heart failure is the structural remodelling of cardiac tissue, including tissue dilation and development of fibrosis. It is therefore important to study these changes and their effect on cardiac activity, in order to gain a better understanding of the underlying mechanisms in arrhythmogenesis, which will hopefully enable us to develop better treatments for heart failure. In this study we developed biophysically detailed models of the rabbit atria for normal and heart failure conditions. These models were used to study the effects of structural remodelling of heart failure on cardiac excitation wave conduction. Anatomical reconstructions of the control and heart failure hearts were based on contrast enhanced micro-CT imaging. Fibre orientation was extracted from the control and heart failure datasets. Effects of heart failure geometry on the activation pattern of atrial excitation waves were analyzed. It was found that atrial activation time increased from the control to the heart failure case in both isotropic and anisotropic conditions, which is attributed primarily to the dilation of tissue caused by heart failure

    NASAwide electronic publishing system: Electronic printing and duplicating, stage-2 evaluation report (GSFC)

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    The NASA Scientific and Technical Information Office was assigned the responsibility to continue with the expansion of the NASAwide networked electronic duplicating effort by including the Goddard Space Flight Center (GSFC) as an additional node to the existing configuration of networked electronic duplicating systems within NASA. The subject of this report is the evaluation of a networked electronic duplicating system which meets the duplicating requirements and expands electronic publishing capabilities without increasing current operating costs. This report continues the evaluation reported in 'NASA Electronic Publishing System - Electronic Printing and Duplicating Evaluation Report' (NASA TM-106242) and 'NASA Electronic Publishing System - Stage 1 Evaluation Report' (NASA TM-106510). This report differs from the previous reports through the inclusion of an external networked desktop editing, archival, and publishing functionality which did not exist with the previous networked electronic duplicating system. Additionally, a two-phase approach to the evaluation was undertaken; the first was a paper study justifying a 90-day, on-site evaluation, and the second phase was to validate, during the 90-day evaluation, the cost benefits and productivity increases that could be achieved in an operational mode. A benchmark of the functionality of the networked electronic publishing system and external networked desktop editing, archival, and publishing system was performed under a simulated daily production environment. This report can be used to guide others in determining the most cost effective duplicating/publishing alternative through the use of cost/benefit analysis and return on investment techniques. A treatise on the use of these techniques can be found by referring to 'NASA Electronic Publishing System -Cost/Benefit Methodology' (NASA TM-106662)

    Hygienic behaviour in the Australian stingless bees Tetragonula carbonaria and T. hockingsi

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    Hygienic behaviour is a natural mechanism of colony-level disease resistance to brood pathogens and has been reported in honey bees and stingless bees. A novel brood disease was recently confirmed in the Australian stingless bees Tetragonula carbonaria Smith and Tetragonula hockingsi Cockerell and there is a paucity of data available on hygienic behaviour in these species. To address this, we investigated hygienic behaviour in eight colonies of T. carbonaria and four colonies of T. hockingsi, using brood freeze-kill and pin-kill assays. Hygienic behaviour was present in both species and was rapidly expressed in both assays. In T. carbonaria, the mean time (± SE) for removal of freeze-killed and pin-killed brood was 9.1 ± 1.9 hours and 8.2 ± 0.9 hours, respectively (n=8; one trial per assay). In T. hockingsi, removal of freeze-killed and pin-killed brood was 14.1 ± 5.1 hours and 10.4 (no SE) hours, respectively. There was no significant difference (α=0.05) in time taken to complete the hygienic behaviour phases (detection, uncapping, removal or cell dismantling) between assay type or assay order in both species. However, intercolony variation was observed in both species in the assays, suggesting that like honey bees, hygienic behaviour may have a genetic component. Tetragonula carbonaria and T. hockingsi displayed significantly faster detection, uncapping, removal and cell dismantling times than any of the stingless bees or most honey bees studied previously. This may, in part, explain why stingless bees appear to suffer from relatively few brood diseases

    Evaluation of sense-strand mRNA amplification by comparative quantitative PCR

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    BACKGROUND: RNA amplification is required for incorporating laser-capture microdissection techniques into microarray assays. However, standard oligonucleotide microarrays contain sense-strand probes, so traditional T7 amplification schemes producing anti-sense RNA are not appropriate for hybridization when combined with conventional reverse transcription labeling methods. We wished to assess the accuracy of a new sense-strand RNA amplification method by comparing ratios between two samples using quantitative real-time PCR (qPCR), mimicking a two-color microarray assay. RESULTS: We performed our validation using qPCR. Three samples of rat brain RNA and three samples of rat liver RNA were amplified using several kits (Ambion messageAmp, NuGen Ovation, and several versions of Genisphere SenseAmp). Results were assessed by comparing the liver/brain ratio for 192 mRNAs before and after amplification. In general, all kits produced strong correlations with unamplified RNAs. The SenseAmp kit produced the highest correlation, and was also able to amplify a partially degraded sample accurately. CONCLUSION: We have validated an optimized sense-strand RNA amplification method for use in comparative studies such as two-color microarrays

    Genetic structure along an elevational gradient in Hawaiian honeycreepers reveals contrasting evolutionary responses to avian malaria

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    <p>Abstract</p> <p>Background</p> <p>The Hawaiian honeycreepers (Drepanidinae) are one of the best-known examples of an adaptive radiation, but their persistence today is threatened by the introduction of exotic pathogens and their vector, the mosquito <it>Culex quinquefasciatus</it>. Historically, species such as the amakihi (<it>Hemignathus virens</it>), the apapane (<it>Himatione sanguinea</it>), and the iiwi (<it>Vestiaria coccinea</it>) were found from the coastal lowlands to the high elevation forests, but by the late 1800's they had become extremely rare in habitats below 900 m. Recently, however, populations of amakihi and apapane have been observed in low elevation habitats. We used twelve polymorphic microsatellite loci to investigate patterns of genetic structure, and to infer responses of these species to introduced avian malaria along an elevational gradient on the eastern flanks of Mauna Loa and Kilauea volcanoes on the island of Hawaii.</p> <p>Results</p> <p>Our results indicate that amakihi have genetically distinct, spatially structured populations that correspond with altitude. We detected very few apapane and no iiwi in low-elevation habitats, and genetic results reveal only minimal differentiation between populations at different altitudes in either of these species.</p> <p>Conclusion</p> <p>Our results suggest that amakihi populations in low elevation habitats have not been recolonized by individuals from mid or high elevation refuges. After generations of strong selection for pathogen resistance, these populations have rebounded and amakihi have become common in regions in which they were previously rare or absent.</p
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