135 research outputs found

    NDT of Composites by Thermography

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    This paper describes ongoing research efforts to evaluate thermographic techniques for locating flaws or damage in structural fiber composite laminates. An infra-red camera with video isotherm readout is used to identify perturbations in uniform or linear thermal fields which may be caused by presence of flaws or damage such as matrix cracks, delaminations, blind side impact damage, and partial through holes. This procedure has potential for rapid qualitative screening of large surface areas. Potential defective areas may then be analyzed by a more accurate (but more time consuming) method . Two techniques are discussed; externally applied thermal field (EATF) and stress-generated thermal field (SGTF). The EATF technique involves applying heat to a composite structure and observing theresulting transient thermal pattern. The SGTF technique requires stress cycling to create hot spots in regions of high stress concentrations adjacent to flaws or damage sites

    A Low Percent Ethanol Method for Immobilizing Planarians

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    Planarians have recently become a popular model system for the study of adult stem cells, regeneration and polarity. The system is attractive for both undergraduate and graduate research labs, since planarian colonies are low cost and easy to maintain. Also in situ hybridization, immunofluorescence and RNA-interference (RNAi) gene knockdown techniques have been developed for planarian studies. However, imaging of live worms (particularly at high magnifications) is difficult because animals are strongly photophobic; they quickly move away from light sources and out of frame. The current methods available to inhibit movement in planarians include RNAi injection and exposure to cold temperatures. The former is labor and time intensive, while the latter precludes the use of many fluorescent reporter dyes. Here, we report a simple, inexpensive and reversible method to immobilize planarians for live imaging. Our data show that a short 1 hour treatment with 3% ethanol (EtOH) is sufficient to inhibit both the fine and gross movements of Schmidtea mediterranea planarians, of the typical size used (4–6 mm), with full recovery of movement within 3–4 hours. Importantly, EtOH treatment did not interfere with regeneration, even after repeated exposure, nor lyse epithelial cells (as assayed by H&E staining). We demonstrate that a short exposure to a low concentration of EtOH is a quick and effective method of immobilizing planarians, one that is easily adaptable to planarians of all sizes and will increase the accessibility of live imaging assays to planarian researchers

    Population structure of the malaria vector Anopheles moucheti in the equatorial forest region of Africa

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    <p>Abstract</p> <p>Background</p> <p><it>Anopheles moucheti </it>is a major malaria vector in forested areas of Africa. However, despite its important epidemiological role, it remains poorly known and insufficiently studied. Here, levels of genetic differentiation were estimated between different <it>A. moucheti </it>populations sampled throughout its distribution range in Central Africa.</p> <p>Methods</p> <p>Polymorphism at ten microsatellite markers was compared in mosquitoes sampled in Cameroon, the Democratic Republic of Congo and an island on Lake Victoria in Uganda. Microsatellite data were used to estimate genetic diversity within populations, their relative long-term effective population size, and the level of genetic differentiation between them.</p> <p>Results</p> <p>All specimens collected in Tsakalakuku (Democratic Republic of Congo) were identified as <it>A. m. bervoetsi </it>while other samples consisted of <it>A. m. moucheti</it>. Successful amplification was obtained at all microsatellite loci within all <it>A. m. moucheti </it>samples while only six loci amplified in <it>A. m. bervoetsi</it>. Allelic richness and heterozygosity were high for all populations except the island population of Uganda and <it>A. m. bervoetsi</it>. High levels of genetic differentiation were recorded between <it>A. m. bervoetsi </it>and each <it>A. m. moucheti </it>sample as well as between the island population of <it>A. m. moucheti </it>and mainland populations. Significant isolation by distance was evidenced between mainland populations.</p> <p>Conclusion</p> <p>High levels of genetic differentiation supports complete speciation of <it>A. m. bervoetsi </it>which should henceforth be recognized as a full species and named <it>A. bervoetsi</it>. Isolation by distance is the main force driving differentiation between mainland populations of <it>A. m. moucheti</it>. Genetically and geographically isolated populations exist on Lake Victoria islands, which might serve as relevant field sites for evaluation of innovative vector control strategies.</p

    Acetate Causes Alcohol Hangover Headache in Rats

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    Background: The mechanism of veisalgia cephalgia or hangover headache is unknown. Despite a lack of mechanistic studies, there are a number of theories positing congeners, dehydration, or the ethanol metabolite acetaldehyde as causes of hangover headache. Methods: We used a chronic headache model to examine how pure ethanol produces increased sensitivity for nociceptive behaviors in normally hydrated rats. Results: Ethanol initially decreased sensitivity to mechanical stimuli on the face (analgesia), followed 4 to 6 hours later by inflammatory pain. Inhibiting alcohol dehydrogenase extended the analgesia whereas inhibiting aldehyde dehydrogenase decreased analgesia. Neither treatment had nociceptive effects. Direct administration of acetate increased nociceptive behaviors suggesting that acetate, not acetaldehyde, accumulation results in hangover-like hypersensitivity in our model. Since adenosine accumulation is a result of acetate formation, we administered an adenosine antagonist that blocked hypersensitivity. Discussion: Our study shows that acetate contributes to hangover headache. These findings provide insight into the mechanism of hangover headache and the mechanism of headache induction

    Identifying an indoor air exposure limit for formaldehyde considering both irritation and cancer hazards

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    Formaldehyde is a well-studied chemical and effects from inhalation exposures have been extensively characterized in numerous controlled studies with human volunteers, including asthmatics and other sensitive individuals, which provide a rich database on exposure concentrations that can reliably produce the symptoms of sensory irritation. Although individuals can differ in their sensitivity to odor and eye irritation, the majority of authoritative reviews of the formaldehyde literature have concluded that an air concentration of 0.3 ppm will provide protection from eye irritation for virtually everyone. A weight of evidence-based formaldehyde exposure limit of 0.1 ppm (100 ppb) is recommended as an indoor air level for all individuals for odor detection and sensory irritation. It has recently been suggested by the International Agency for Research on Cancer (IARC), the National Toxicology Program (NTP), and the US Environmental Protection Agency (US EPA) that formaldehyde is causally associated with nasopharyngeal cancer (NPC) and leukemia. This has led US EPA to conclude that irritation is not the most sensitive toxic endpoint and that carcinogenicity should dictate how to establish exposure limits for formaldehyde. In this review, a number of lines of reasoning and substantial scientific evidence are described and discussed, which leads to a conclusion that neither point of contact nor systemic effects of any type, including NPC or leukemia, are causally associated with exposure to formaldehyde. This conclusion supports the view that the equivocal epidemiology studies that suggest otherwise are almost certainly flawed by identified or yet to be unidentified confounding variables. Thus, this assessment concludes that a formaldehyde indoor air limit of 0.1 ppm should protect even particularly susceptible individuals from both irritation effects and any potential cancer hazard

    NDT of Composites by Thermography

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    This paper describes ongoing research efforts to evaluate thermographic techniques for locating flaws or damage in structural fiber composite laminates. An infra-red camera with video isotherm readout is used to identify perturbations in uniform or linear thermal fields which may be caused by presence of flaws or damage such as matrix cracks, delaminations, blind side impact damage, and partial through holes. This procedure has potential for rapid qualitative screening of large surface areas. Potential defective areas may then be analyzed by a more accurate (but more time consuming) method . Two techniques are discussed; externally applied thermal field (EATF) and stress-generated thermal field (SGTF). The EATF technique involves applying heat to a composite structure and observing theresulting transient thermal pattern. The SGTF technique requires stress cycling to create hot spots in regions of high stress concentrations adjacent to flaws or damage sites.</p

    NDT of Composites by Thermography

    No full text
    This paper describes ongoing research efforts to evaluate thermographic techniques for locating flaws or damage in structural fiber composite laminates. An infra-red camera with video isotherm readout is used to identify perturbations in uniform or linear thermal fields which may be caused by presence of flaws or damage such as matrix cracks, delaminations, blind side impact damage, and partial through holes. This procedure has potential for rapid qualitative screening of large surface areas. Potential defective areas may then be analyzed by a more accurate (but more time consuming) method . Two techniques are discussed; externally applied thermal field (EATF) and stress-generated thermal field (SGTF). The EATF technique involves applying heat to a composite structure and observing theresulting transient thermal pattern. The SGTF technique requires stress cycling to create hot spots in regions of high stress concentrations adjacent to flaws or damage sites.</p
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