2,855 research outputs found
Convention for the Protection of Cultural Property in the Event of Armed Conflict: 70th Anniversary Information Pack
Founded in 1996, today, the Blue Shield Movement works around the world to protect all types of threatened cultural heritage in conflict, but also in crisis, unrest, and following disaster. This anniversary is an opportunity to raise awareness about the Convention and its obligations, to push for ratification in countries which are not yet party to these vital laws, and to showcase the work and importance of the Blue Shield Movement as we reflect on 70 years of successes and challenges of the Convention, and look towards the future.This Information Pack is aimed at Blue Shield National Committees, but contains information anyone interested in the history of the Convention will find useful. It provides information about the 1954 Hague Convention and its Protocols – what they are, and why they matter? How are they linked to the Blue Shield? What are the obligations on States Parties to help protect heritage in conflict
Aerial photography collected with a multirotor drone reveals impact of Eurasian beaver reintroduction on ecosystem structure
doi: 10.1139/juvs-2015-0005Copyright © 2015 Canadian Science PublishingBeavers are often described as ecological engineers with an ability to modify the structure and flow of fluvial systems and create complex wetland environments with dams, ponds and canals. Consequently, beaver activity has implications for a wide range of environmental ecosystem services including biodiversity, flood risk mitigation, water quality and sustainable drinking water provision. With the current debate surrounding the reintroduction of beavers into the United Kingdom, it is critical to be able to monitor the impact of beavers upon the environment. This study presents the first proof of concept results showing how a lightweight hexacopter fitted with a simple digital camera can be used to derive orthophoto and digital surface model (DSM) data products at a site where beavers have recently been reintroduced. Early results indicate that analysis of the fine-scale (0.01 m) orthophoto and DSM can be used to identify impacts on the ecosystem structure including the extent of dams and associated ponds, and changes in vegetation structure due to beaver tree felling activity. Unmanned aerial vehicle data acquisition offers an effective toolkit for regular repeat monitoring at fine spatial resolution which is a critical attribute for monitoring rapidly-changing and difficult to access beaver-impacted ecosystems
Context-specific gene regulatory networks subdivide intrinsic subtypes of breast cancer
<p>Abstract</p> <p>Background</p> <p>Breast cancer is a highly heterogeneous disease with respect to molecular alterations and cellular composition making therapeutic and clinical outcome unpredictable. This diversity creates a significant challenge in developing tumor classifications that are clinically reliable with respect to prognosis prediction.</p> <p>Results</p> <p>This paper describes an unsupervised context analysis to infer context-specific gene regulatory networks from 1,614 samples obtained from publicly available gene expression data, an extension of a previously published methodology. We use the context-specific gene regulatory networks to classify the tumors into clinically relevant subgroups, and provide candidates for a finer sub-grouping of the previously known intrinsic tumors with a focus on Basal-like tumors. Our analysis of pathway enrichment in the key contexts provides an insight into the biological mechanism underlying the identified subtypes of breast cancer.</p> <p>Conclusions</p> <p>The use of context-specific gene regulatory networks to identify biological contexts from heterogenous breast cancer data set was able to identify genomic drivers for subgroups within the previously reported intrinsic subtypes. These subgroups (contexts) uphold the clinical relevant features for the intrinsic subtypes and were associated with increased survival differences compared to the intrinsic subtypes. We believe our computational approach led to the generation of novel rationalized hypotheses to explain mechanisms of disease progression within sub-contexts of breast cancer that could be therapeutically exploited once validated.</p
Latitudinal variation in the potential activity of Atlantic Ocean bacterioplankton revealed through 16S rRNA and 16S rRNA gene metabarcoding
The activities of bacterioplankton sustain open ocean biogeochemical and ecological processes, however, little is known about the activity of specific bacterioplankton, especially related to their biogeography across oceanic scales. The Atlantic is the second largest of the world’s oceans and has an essential role in the global carbon cycle. Here, we show congruence in the structure of 16S rRNA and 16S rRNA gene derived bacterioplankton communities throughout the Atlantic Ocean from temperate to tropical regions. We used 16S rRNA:16S rRNA gene ratios as a phylogenetically resolved proxy for potential activity, demonstrating ocean-scale patterns of putative oligotrophy and copiotrophy in major bacterioplankton groups, with spatial niche partitioning being evident at single-nucleotide resolution within some groups, including the Flavobacteria and SAR86. This study examines the potential structure of the active microbiome of the Atlantic Ocean, providing novel insights into the ecology and life history strategies of both well-known and currently understudied bacterioplankton taxa
Quantification of Cellular Proliferation in Acne Using the Monoclonal Antibody Ki-67
The mechanism by which ductal hypercornification occurs in acne is uncertain. We investigated proliferation in normal and acne follicles and in the interfollicular epidermis using the monoclonal antibody Ki-67, which reacts with a nuclear antigen expressed by cells in the G1, S, M, and G2 phases of the cell cycle. Cryostat sections of biopsies from the interscapular region from acne patients and from normal volunteers were stained with Ki-67 antibody and counterstained with 2% methyl green. The number of Ki-67-positive nuclei in the basal layer were counted and expressed as a percentage of the total number of basal nuclei in the ductal or interfollicular epithelia. The data was expressed as mean percent ± SD. In normal follicles from acne-affected sites 17.40% ± 1.86% (n = 8) of the nuclei were Ki-67 positive. This was significantly higher (p <0.01) than follicles from an area of skin unaffected by acne (11.01% ± 6.16%, n = 8). In the follicular epithelia of non-inflamed lesions, the percentage of Ki-67 positive nuclei was 23.44% ± 8.36% (n = 15). It was impossible to count the nuclei of follicular epithelium of inflamed lesions because little of this remained intact. In normal interfollicular epidermis, Ki-67-positive nuclei represented 5.33% ± 3.36% (n = 8) of the total. This value was not significantly different from the value obtained for interfollicular epidermis near non-inflamed lesions (10.46% ± 4.45%, n = 15). However, the number of Ki- 67-positive nuclei in the interfollicular epidermis near inflamed lesions was significantly higher than either of these two values: 25.26% ± 6.83%, n = 13, p < 0.05. Our results with Ki-67 confirm that ductal hyperproliferation occurs in acne and shows that normal follicles from acne skin may be “acne-prone.
Bidirectional crosstalk between hypoxia-inducible factor and glucocorticoid signalling in zebrafish larvae
In the last decades in vitro studies highlighted the potential for crosstalk between Hypoxia-Inducible Factor-(HIF) and glucocorticoid-(GC) signalling pathways. However, how this interplay precisely occurs in vivo is still debated. Here, we use zebrafish larvae (Danio rerio) to elucidate how and to what degree hypoxic signalling affects the endogenous glucocorticoid pathway and vice versa, in vivo. Firstly, our results demonstrate that in the presence of upregulated HIF signalling, both glucocorticoid receptor (Gr) responsiveness and endogenous cortisol levels are repressed in 5 days post fertilisation larvae. In addition, despite HIF activity being low at normoxia, our data show that it already impedes both glucocorticoid activity and levels. Secondly, we further analysed the in vivo contribution of glucocorticoids to HIF activity. Interestingly, our results show that both glucocorticoid receptor (GR) and mineralocorticoid receptor (MR) play a key role in enhancing it. Finally, we found indications that glucocorticoids promote HIF signalling via multiple routes. Cumulatively, our findings allowed us to suggest a model for how this crosstalk occurs in vivo
- …