403 research outputs found

    An autoethnography of lifestories recorded on the community radio on the island of Barra

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    In agreeing with Geertz’s claim that culture is experiential (1973), I aim to present an interpretation of a lived experience. It is an autoethnographic reflection of my experience as a volunteer radio host for the community radio station on the island of Barra in the Outer Hebrides of Scotland. At the heart of my argument is spoken language and its meaning. From a selection of themes of transcribed lifestory interviews, I aim to show that culture, diachronically shaped in the island’s collective historical experience of its past relationship to the sea, transforms itself through language to create a coherency of our present living experience. Indeed, my argument is that the collective conceptualisation of community and tradition, and the more individualised concept of identity, as conduits of culture, are constructed through contextually significant linear and non-linear narrative language, which is the result of temporal, ever-changing phenomenological processes. This synchronic interpretation, based on a snapshot of a collective public space, uses a critical discourse analysis of the island’s oral history to demonstrate how lifestory narratives reflect and refract coherency of a historical specific time. In such slightly skewed reflections, the locality finds itself. But in its refracted form, it moves beyond the parochial into territory where themes uncover age gender differences. The differentiation of meaning produces a coherency that is echoed in feminist discourse. Looking through the theoretical lenses of anthropological and sociological perspectives, I argue that in the construction of lifestory narratives, the power relationships of a wider capitalist society are embedded, and, as such, reflect our lived experience, which gives meaning to what we understand as culture

    Identification of diagnostic upper gastrointestinal cancer tissue type‑specific urinary biomarkers

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    Several potential urinary biomarkers exhibiting an association with upper gastrointestinal tumour growth have been previously identified, of which S100A6, S100A9, rabenosyn‑5 and programmed cell death 6‑interacting protein (PDCD6IP) were further validated and found to be upregulated in malignant tumours. The cancer cohort from our previous study was subclassified to assess whether distinct molecular markers can be identified for each individual cancer type using a similar approach. Urine samples from patients with cancers of the stomach, oesophagus, oesophagogastric junction or pancreas were analysed by surface‑enhanced laser desorption/ionization‑time‑of‑flight mass spectrometry using both CM10 and IMAC30 (Cu2+‑complexed) chip types and LC‑MS/MS‑based mass spectrometry after chromatographic enrichment. This was followed by protein identification, pattern matching and validation by western blotting. We found 8 m/z peaks with statistical significance for the four cancer types investigated, of which m/z 2447 and 2577 were identified by pattern matching as fragments of cathepsin‑B (CTSB) and cystatin‑B (CSTB); both molecules are indicative of pancreatic cancer. Additionally, we observed a potential association of upregulated α‑1‑antichymotrypsin with pancreatic and gastric cancers, of PDCD6IP, vitelline membrane outer layer protein 1 homolog (VMO1) and triosephosphate isomerase (TPI1) with oesophagogastric junctional cancers, and of complement C4‑A, prostatic acid phosphatase, azurocidin and histone‑H1 with oesophageal cancer. Furthermore, the potential pancreatic cancer biomarkers CSTB and CTSB were validated independently by western blotting. Therefore, the present study identified two new potential urinary biomarkers that appear to be associated with pancreatic cancer. This may provide a simple, non‑invasive screening test for use in the clinical setting.</p

    Hubble Space Telescope Grism Spectroscopy of Extreme Starbursts Across Cosmic Time: The Role of Dwarf Galaxies in the Star Formation History of the Universe

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    Near infrared slitless spectroscopy with the Wide Field Camera 3, onboard the Hubble Space Telescope, offers a unique opportunity to study low-mass galaxy populations at high-redshift (z∌z\sim1-2). While most high−z-z surveys are biased towards massive galaxies, we are able to select sources via their emission lines that have very-faint continua. We investigate the star formation rate (SFR)-stellar mass (M⋆M_{\star}) relation for about 1000 emission-line galaxies identified over a wide redshift range of 0.3â‰Čzâ‰Č2.30.3 \lesssim z \lesssim 2.3. We use the Hα_{\alpha} emission as an accurate SFR indicator and correct the broadband photometry for the strong nebular contribution to derive accurate stellar masses down to M⋆∌107M⊙M_{\star} \sim 10^{7} M_{\odot}. We focus here on a subsample of galaxies that show extremely strong emission lines (EELGs) with rest-frame equivalent widths ranging from 200 to 1500 \AA. This population consists of outliers to the normal SFR-M⋆M_{\star} sequence with much higher specific SFRs (>10> 10 Gyr−1^{-1}). While on-sequence galaxies follow a continuous star formation process, EELGs are thought to be caught during an extreme burst of star formation that can double their stellar mass in less than 100100 Myr. The contribution of starbursts to the total star formation density appears to be larger than what has been reported for more massive galaxies in previous studies. In the complete mass range 8.2<8.2 < log(M⋆/M⊙M_{\star}/M_{\odot}) <10< 10 and a SFR lower completeness limit of about 2 M⊙M_{\odot} yr−1^{-1} (10 M⊙M_{\odot} yr−1^{-1}) at z∌1z\sim1 (z∌2z \sim 2), we find that starbursts having EWrest_{rest}(Hα_{\alpha})>> 300, 200, and 100 A contribute up to ∌13\sim13, 18, and 34 %, respectively, to the total SFR of emission-line selected sample at z∌1−2z\sim1-2. The comparison with samples of massive galaxies shows an increase in the contribution of starbursts towards lower masses.Comment: 11 pages, 6 figures. The Astrophysical Journal, in pres

    Molecular profiling of multiplexed gene markers to assess viability of ex vivo human colon explant cultures

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    © Janice E. Drew et al. 2015; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. Acknowledgments The authors would like to thank the patients who kindly donated tissue samples, Sally Chalmers of the Tayside Tissue Bank for her help with collecting of the tissue donor samples, Emma Moss for advice on human colon dissection and explant culture, and Claus Dieter Mayer, Biomathematics and Statistics Scotland, for advice on statistical analysis. This work was supported by the Scottish Government (GT403), Scottish Universities Life Science Alliance, and TENOVUS Scotland.Peer reviewedPublisher PD
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