777 research outputs found

    Common Eider (Somateria mollissima v-nigrum) Nest Cover and Depredation on Central Alaskan Beaufort Sea Barrier Islands

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    Female common eiders (Somateria mollissima v-nigrum) generally select nest sites in areas with driftwood cover. Previous studies of common eiders have shown a positive relationship between nest success and driftwood cover. Our observations led us to hypothesize that cover does not enhance nest success when mammalian predators are present. To evaluate nest cover selection in common eiders, we examined five years of nesting data to determine the interactions between the probability of nest activity and the amount of driftwood cover in the presence of avian versus mammalian predators. Most common eider nests were surrounded by low (40%) or moderate (38%) driftwood cover. Nest failure rates were high (32%– 95%), and arctic foxes (Alopex lagopus), alone or with polar bears (Ursus maritimus), appeared to be more destructive than glaucous gulls (Larus hyperboreus) to eider nests. Logistic regression was used to model common eider nest activity associated with driftwood cover and predators. When glaucous gulls were the only predators, more driftwood cover consistently increased the probability of nest activity. But when foxes were present, nest activity consistently decreased with increasing cover. Our models support our observations that nest cover was beneficial to eiders when glaucous gulls alone were predators. Driftwood cover may be most important for the thermal and structural protection it offers, rather than for the camouflage it provides. The energetic benefit provided by driftwood windbreaks coupled with the common eider’s behavioral response of decreased nest attendance, or increased exposure to avian depredation of nests as energy reserves are depleted during incubation, provides an explanatory mechanism for our model results.L’eider Ă  duvet femelle (Somateria mollissima v-nigrum) choisit en gĂ©nĂ©ral son site de nidification dans des zones ayant un couvert de bois flottĂ©. Des Ă©tudes prĂ©cĂ©dentes sur les eiders Ă  duvet ont rĂ©vĂ©lĂ© qu’il existe une relation positive entre le succĂšs de la couvĂ©e et le couvert de bois flottĂ©. Nos observations nous ont amenĂ©s Ă  Ă©mettre l’hypothĂšse que le couvert n’augmente pas le succĂšs de la couvĂ©e en prĂ©sence de prĂ©dateurs mammifĂšres. Afin d’évaluer le choix de couvert du nid chez l’eider Ă  duvet, nous avons examinĂ© des donnĂ©es de nidification obtenues sur cinq annĂ©es, en vue de dĂ©gager les interactions entre la probabilitĂ© d’activitĂ© au nid et la quantitĂ© de couvert de bois flottĂ© en prĂ©sence de prĂ©dateurs aviens par opposition aux prĂ©dateurs mammifĂšres. La plupart des nids de l’eider Ă  duvet Ă©taient entourĂ©s par un faible couvert de bois flottĂ© (40 %) ou un couvert modĂ©rĂ© (38 %). Les taux d’insuccĂšs Ă©taient Ă©levĂ©s (32 Ă  95 %) et le renard arctique (Alopex lagopus), seul ou avec l’ours polaire (Ursus maritimus), semblait plus destructeur pour les nids de l’eider que le goĂ©land bourgmestre (Larus hyperboreus). On a utilisĂ© la rĂ©gression logistique pour simuler l’activitĂ© au nid de l’eider Ă  duvet associĂ©e au couvert de bois flottĂ© et aux prĂ©dateurs. Quand le goĂ©land bourgmestre Ă©tait le seul prĂ©dateur, une plus grande quantitĂ© de bois flottĂ© augmentait toujours la probabilitĂ© d’activitĂ© au nid. En revanche, en prĂ©sence du renard, l’activitĂ© au nid diminuait toujours avec une augmentation du couvert. Nos modĂšles viennent appuyer nos observations Ă  l’effet que le couvert du nid reprĂ©sentait un avantage pour l’eider quand le goĂ©land bourgmestre Ă©tait le seul prĂ©dateur. Le couvert de bois flottĂ© pourrait bien ĂȘtre d’une importance capitale en raison de la protection thermique et structurale qu’il offre, plutĂŽt que pour ses capacitĂ©s de camouflage. L’avantage Ă©nergĂ©tique qu’offrent les brise-vent de bois flottĂ© joint Ă  la rĂ©action comportementale de l’eider Ă  duvet – qui se manifeste par une plus grande prĂ©sence au nid, ou une plus grande exposition Ă  une dĂ©prĂ©dation avienne du nid Ă  mesure que s’épuisent les rĂ©serves d’énergie durant l’incubation –, ces deux Ă©lĂ©ments donc fournissent un mĂ©canisme pouvant expliquer les rĂ©sultats de notre modĂšle

    Tissue-specific calibration of extracellular matrix material properties by transforming growth factor-beta and Runx2 in bone is required for hearing

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    Publisher version: http://www.nature.com/embor/journal/v11/n10/full/embor2010135.htmlDA - 20100917 IS - 1469-3178 (Electronic) IS - 1469-221X (Linking) LA - ENG PT - JOURNAL ARTICLEDA - 20100917 IS - 1469-3178 (Electronic) IS - 1469-221X (Linking) LA - ENG PT - JOURNAL ARTICLEDA - 20100917 IS - 1469-3178 (Electronic) IS - 1469-221X (Linking) LA - ENG PT - JOURNAL ARTICLEPhysical cues, such as extracellular matrix stiffness, direct cell differentiation and support tissue-specific function. Perturbation of these cues underlies diverse pathologies, including osteoarthritis, cardiovascular disease and cancer. However, the molecular mechanisms that establish tissue-specific material properties and link them to healthy tissue function are unknown. We show that Runx2, a key lineage-specific transcription factor, regulates the material properties of bone matrix through the same transforming growth factor-beta (TGFbeta)-responsive pathway that controls osteoblast differentiation. Deregulated TGFbeta or Runx2 function compromises the distinctly hard cochlear bone matrix and causes hearing loss, as seen in human cleidocranial dysplasia. In Runx2(+/-) mice, inhibition of TGFbeta signalling rescues both the material properties of the defective matrix, and hearing. This study elucidates the unknown cause of hearing loss in cleidocranial dysplasia, and demonstrates that a molecular pathway controlling cell differentiation also defines material properties of extracellular matrix. Furthermore, our results suggest that the careful regulation of these properties is essential for healthy tissue functio

    Utility of the pooling approach as applied to whole genome association scans with high-density Affymetrix microarrays

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    Background: We report an attempt to extend the previously successful approach of combining SNP (single nucleotide polymorphism) microarrays and DNA pooling (SNP-MaP) employing high-density microarrays. Whereas earlier studies employed a range of Affymetrix SNP microarrays comprising from 10 K to 500 K SNPs, this most recent investigation used the 6.0 chip which displays 906,600 SNP probes and 946,000 probes for the interrogation of CNVs (copy number variations). The genotyping assay using the Affymetrix SNP 6.0 array is highly demanding on sample quality due to the small feature size, low redundancy, and lack of mismatch probes. Findings: In the first study published so far using this microarray on pooled DNA, we found that pooled cheek swab DNA could not accurately predict real allele frequencies of the samples that comprised the pools. In contrast, the allele frequency estimates using blood DNA pools were reasonable, although inferior compared to those obtained with previously employed Affymetrix microarrays. However, it might be possible to improve performance by developing improved analysis methods. Conclusions: Despite the decreasing costs of genome-wide individual genotyping, the pooling approach may have applications in very large-scale case-control association studies. In such cases, our study suggests that high-quality DNA preparations and lower density platforms should be preferred

    Spin Caloritronics

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    This is a brief overview of the state of the art of spin caloritronics, the science and technology of controlling heat currents by the electron spin degree of freedom (and vice versa).Comment: To be published in "Spin Current", edited by S. Maekawa, E. Saitoh, S. Valenzuela and Y. Kimura, Oxford University Pres

    Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs

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    BACKGROUND: Classical genetic studies indicate that nicotine dependence is a substantially heritable complex disorder. Genetic vulnerabilities to nicotine dependence largely overlap with genetic vulnerabilities to dependence on other addictive substances. Successful abstinence from nicotine displays substantial heritable components as well. Some of the heritability for the ability to quit smoking appears to overlap with the genetics of nicotine dependence and some does not. We now report genome wide association studies of nicotine dependent individuals who were successful in abstaining from cigarette smoking, nicotine dependent individuals who were not successful in abstaining and ethnically-matched control subjects free from substantial lifetime use of any addictive substance. RESULTS: These data, and their comparison with data that we have previously obtained from comparisons of four other substance dependent vs control samples support two main ideas: 1) Single nucleotide polymorphisms (SNPs) whose allele frequencies distinguish nicotine-dependent from control individuals identify a set of genes that overlaps significantly with the set of genes that contain markers whose allelic frequencies distinguish the four other substance dependent vs control groups (p < 0.018). 2) SNPs whose allelic frequencies distinguish successful vs unsuccessful abstainers cluster in small genomic regions in ways that are highly unlikely to be due to chance (Monte Carlo p < 0.00001). CONCLUSION: These clustered SNPs nominate candidate genes for successful abstinence from smoking that are implicated in interesting functions: cell adhesion, enzymes, transcriptional regulators, neurotransmitters and receptors and regulation of DNA, RNA and proteins. As these observations are replicated, they will provide an increasingly-strong basis for understanding mechanisms of successful abstinence, for identifying individuals more or less likely to succeed in smoking cessation efforts and for tailoring therapies so that genotypes can help match smokers with the treatments that are most likely to benefit them

    An Attribute-Based Approach to Classifying Community-Based Tourism Networks

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    This conceptual paper proposes the adoption of a collaborative network approach as a prospective means of improving success in implementing community-based tourism (CBT) initiatives. Drawing upon relevant literature, the researchers identify the key attributes that characterise a network-based approach. By proposing alternatives for each attribute, the research provides CBT practitioners with options for making informed decisions about how to build collaboration connecting individual CBT initiatives in multiple locations. The researchers discuss the implications of different approaches for power relations between stakeholders. The proposed framework provides a means of classifying existing CBT networks and analyses the types of network and the circumstances which lead to better outcomes for community development. Further empirical research is required to test the validity of the key network attributes and to develop a comprehensive classification system of CBT networks.School of Hotel and Tourism Managemen

    Development of a novel monoclonal antibody with reactivity to a wide range of Venezuelan equine encephalitis virus strains

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    <p>Abstract</p> <p>Background</p> <p>There is currently a requirement for antiviral therapies capable of protecting against infection with Venezuelan equine encephalitis virus (VEEV), as a licensed vaccine is not available for general human use. Monoclonal antibodies are increasingly being developed as therapeutics and are potential treatments for VEEV as they have been shown to be protective in the mouse model of disease. However, to be truly effective, the antibody should recognise multiple strains of VEEV and broadly reactive monoclonal antibodies are rarely and only coincidentally isolated using classical hybridoma technology.</p> <p>Results</p> <p>In this work, methods were developed to reliably derive broadly reactive murine antibodies. A phage library was created that expressed single chain variable fragments (scFv) isolated from mice immunised with multiple strains of VEEV. A broadly reactive scFv was identified and incorporated into a murine IgG2a framework. This novel antibody retained the broad reactivity exhibited by the scFv but did not possess virus neutralising activity. However, the antibody was still able to protect mice against VEEV disease induced by strain TrD when administered 24 h prior to challenge.</p> <p>Conclusion</p> <p>A monoclonal antibody possessing reactivity to a wide range of VEEV strains may be of benefit as a generic antiviral therapy. However, humanisation of the murine antibody will be required before it can be tested in humans.</p> <p>Crown Copyright © 2009</p

    Three-Dimensional Structure of the Enveloped Bacteriophage Ω12: An Incomplete T = 13 Lattice Is Superposed on an Enclosed T = 1 Shell

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    BACKGROUND:Bacteriophage phi12 is a member of the Cystoviridae, a unique group of lipid containing membrane enveloped bacteriophages that infect the bacterial plant pathogen Pseudomonas syringae pv. phaseolicola. The genomes of the virus species contain three double-stranded (dsRNA) segments, and the virus capsid itself is organized in multiple protein shells. The segmented dsRNA genome, the multi-layered arrangement of the capsid and the overall viral replication scheme make the Cystoviridae similar to the Reoviridae. METHODOLOGY/PRINCIPAL FINDINGS:We present structural studies of cystovirus phi12 obtained using cryo-electron microscopy and image processing techniques. We have collected images of isolated phi12 virions and generated reconstructions of both the entire particles and the polymerase complex (PC). We find that in the nucleocapsid (NC), the phi12 P8 protein is organized on an incomplete T = 13 icosahedral lattice where the symmetry axes of the T = 13 layer and the enclosed T = 1 layer of the PC superpose. This is the same general protein-component organization found in phi6 NC's but the detailed structure of the entire phi12 P8 layer is distinct from that found in the best classified cystovirus species phi6. In the reconstruction of the NC, the P8 layer includes protein density surrounding the hexamers of P4 that sit at the 5-fold vertices of the icosahedral lattice. We believe these novel features correspond to dimers of protein P7. CONCLUSIONS/SIGNIFICANCE:In conclusion, we have determined that the phi12 NC surface is composed of an incomplete T = 13 P8 layer forming a net-like configuration. The significance of this finding in regard to cystovirus assembly is that vacancies in the lattice could have the potential to accommodate additional viral proteins that are required for RNA packaging and synthesis

    Enablers and Barriers to Implementing ICU Follow-Up Clinics and Peer Support Groups Following Critical Illness: The Thrive Collaboratives

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    OBJECTIVES: Data are lacking regarding implementation of novel strategies such as follow-up clinics and peer support groups, to reduce the burden of postintensive care syndrome. We sought to discover enablers that helped hospital-based clinicians establish post-ICU clinics and peer support programs, and identify barriers that challenged them. DESIGN: Qualitative inquiry. The Consolidated Framework for Implementation Research was used to organize and analyze data. SETTING: Two learning collaboratives (ICU follow-up clinics and peer support groups), representing 21 sites, across three continents. SUBJECTS: Clinicians from 21 sites. MEASUREMENT AND MAIN RESULTS: Ten enablers and nine barriers to implementation of "ICU follow-up clinics" were described. A key enabler to generate support for clinics was providing insight into the human experience of survivorship, to obtain interest from hospital administrators. Significant barriers included patient and family lack of access to clinics and clinic funding. Nine enablers and five barriers to the implementation of "peer support groups" were identified. Key enablers included developing infrastructure to support successful operationalization of this complex intervention, flexibility about when peer support should be offered, belonging to the international learning collaborative. Significant barriers related to limited attendance by patients and families due to challenges in creating awareness, and uncertainty about who might be appropriate to attend and target in advertising. CONCLUSIONS: Several enablers and barriers to implementing ICU follow-up clinics and peer support groups should be taken into account and leveraged to improve ICU recovery. Among the most important enablers are motivated clinician leaders who persist to find a path forward despite obstacles
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