Representing ideal kinship in Medieval English literature before and after the Norman Conquest

Medieval English literature is often concerned with kingship, its duties, and its effects. Writers used their texts to reflect on and respond to contemporary political issues, and debated the nature of kingship extensively. This thesis explores the development of conceptions of kingship through four case studies, each centring on a specific text or group of texts: Beowulf, the Alfredian Group, twelfth-century Arthurian literature, and Havelok the Dane. This thesis argues that ideas about kingship expressed in these texts often built on the (re-imagined) past in order to comment on present-day issues concerning rulership. As a result, narratives of kingship formed part of an on-going dialogue between these authors, their contemporary contexts, the past, and a desired future. While the Norman Conquest of 1066 resulted in significant discontinuity in cultural and political life in England, it did not provide a clean break with the preConquest past. Indeed, the Anglo-Norman elite and their authors demonstrated great interest in their predecessors and in the land they had conquered. Twelfth- and thirteenthcentury vernacular literature stands testament to this interest, and demonstrates continuities in notions of kingship that can be traced to pre-Conquest texts such as Beowulf. This thesis argues, then, that earlier conceptions of kingship did not cease to exist with the Norman Conquest; the arrival of the Normans did not constitute the implementation of a new ideal of kingship. Instead, pre-Conquest ideas about rulership were reshaped and adapted to suit new audiences, and with different aims. This thesis demonstrates that these developments emphasise the versatility of medieval English literature in reflecting on and responding to emerging and shifting narratives of kingship

Fourth-order discrete-time variable centre frequency bandpass sigma-delta modulator

Copyright © 2006 IEEEA design for a variable centre frequency bandpass sigma-delta modulator is presented. The modulator is based on a tunable discrete-time resonator using only one control parameter. The noise transfer function of the modulator is controlled by a 4-bit digital signal, which provides nine different centre frequencies distributed between 0.1-0.4 normalized frequencies. The measurement results show a stable modulator at all centre frequenciesY. Zhu, S.F. Al-Sarawi, C. C. Lim, and M.J. Liebel

Pharmacological And Genetic Reversal Of Age-Dependent Cognitive Deficits Attributable To Decreased Presenilin Function

Alzheimer\u27s disease (AD) is the leading cause of cognitive loss and neurodegeneration in the developed world. Although its genetic and environmental causes are not generally known, familial forms of the disease (FAD) are attributable to mutations in a single copy of the Presenilin (PS) and amyloid precursor protein genes. The dominant inheritance pattern of FAD indicates that it may be attributable to gain or change of function mutations. Studies of FAD-linked forms of presenilin (psn) in model organisms, however, indicate that they are loss of function, leading to the possibility that a reduction in PS activity might contribute to FAD and that proper psn levels are important for maintaining normal cognition throughout life. To explore this issue further, we have tested the effect of reducing psn activity during aging in Drosophila melanogaster males. We have found that flies in which the dosage of psn function is reduced by 50% display age-onset impairments in learning and memory. Treatment with metabotropic glutamate receptor (mGluR) antagonists or lithium during the aging process prevented the onset of these deficits, and treatment of aged flies reversed the age-dependent deficits. Genetic reduction of Drosophila metabotropic glutamate receptor (DmGluRA), the inositol trisphosphate receptor (InsP(3)R), or inositol polyphosphate 1-phosphatase also prevented these age-onset cognitive deficits. These findings suggest that reduced psn activity may contribute to the age-onset cognitive loss observed with FAD. They also indicate that enhanced mGluR signaling and calcium release regulated by InsP(3)R as underlying causes of the age-dependent cognitive phenotypes observed when psn activity is reduced

Social presence and dishonesty in retail

Self-service checkouts (SCOs) in retail can benefit consumers and retailers, providing control and autonomy to shoppers independent from staff, together with reduced queuing times. Recent research indicates that the absence of staff may provide the opportunity for consumers to behave dishonestly, consistent with a perceived lack of social presence. This study examined whether a social presence in the form of various instantiations of embodied, visual, humanlike SCO interface agents had an effect on opportunistic behaviour. Using a simulated SCO scenario, participants experienced various dilemmas in which they could financially benefit themselves undeservedly. We hypothesised that a humanlike social presence integrated within the checkout screen would receive more attention and result in fewer instances of dishonesty compared to a less humanlike agent. This was partially supported by the results. The findings contribute to the theoretical framework in social presence research. We concluded that companies adopting self-service technology may consider the implementation of social presence in technology applications to support ethical consumer behaviour, but that more research is required to explore the mixed findings in the current study.<br/

From Victims of Trafficking to Freedom Fighters: Rethinking Migrant Domestic Workers in the Middle East

Throughout the Middle East migrant women are employed to work in people’s homes. While some experience good working relations with employers, others experience forms of abuse and labour coercion. This chapter evaluates critically different ways that system of unfree labour has been variously described and analysed as a form of ‘contract slavery’, ‘debt bondage’ and ‘trafficking’. It also shows how migrant women who describe themselves as ‘freelancers’ exit their original employer’s home both to escape that relation and in hopes of securing a better situation outside of the regular system of employment. Freelancing is more than simply a form of resistance. Rather, women who work as freelance migrant domestic workers challenge directly that state enforced control over their mobility and are on the vanguard of those migrants who are seeking through their own actions to effect social change

N and C Isotope Variations Along an Extreme Eutrophication and Salinity Gradient in the Coorong Lagoon, South Australia

The Coorong Lagoon is a unique hydrological and depositional system at the terminus of the Murray–Darling Basin, the largest river system in Australia. It exhibits large salinity, nutrient, and organic matter gradients, providing a modern analogue to study and validate the use of δ15N and δ13C as tracers of past and contemporary geochemical cycles in estuarine environments. To this end, water and surface sediment samples were analyzed for particulate organic nitrogen (PON) and carbon (POC) concentrations, and the respective δ15N and δ13C signatures of particulate nitrogen and carbon. PON and POC exhibited positive relationships to chlorophyll-a, indicating the dominance of phytoplankton production upon suspended organic matter. There was also a general trend of increasing δ15N of PON (δ15NPON) values and decreasing δ13C of particulate carbon (δ13CPC) values with increasing salinity and eutrophication in the restricted South Lagoon. In a multiple linear regression for δ15NPON, the best two predictors in combination are PON and C:N molar ratio, highlighting the importance of productivity and the type or source of organic matter. For δ13CPC, the best two predictors are total dissolved phosphorus and latitude, suggesting influences from productivity and proximity to the ocean. Sediment δ15N values across the Coorong Lagoon overlap with the δ15NPON in the water column, suggesting that PON derived from algal material represents the main source of nitrogen to lagoon sediments. We hypothesize that limited N loss via denitrification leads to PON being recycled almost exclusively to ammonium, due to low rates of nitrification and dominance of dissimilatory nitrate reduction to ammonium (DNRA). We propose that preferential volatilization of 14N in ammonia increases the δ15N of ammonium assimilated by phytoplankton, thereby increasing the δ15N within suspended organic matter and surface sediment in the South Lagoon. By contrast, the gradient exhibited in δ13CPC data was countered by a relatively constant sedimentary organic carbon δ13C. Data from the Coorong, therefore, suggest that δ15N values in sediments can be used to infer palaeoproductivity in this hypereutrophic and hypersaline depositional environment, however, the measured δ13CPC may be influenced by δ13CDIC or preferential loss of 13C during sedimentation that alter the sedimentary δ13C record of organic carbon.Stacey C. Priestley, Jonathan Tyler, Savannah R. Liebelt, Luke M. Mosley, Wei Wen Wong, Yuexiao Shao, Zara Woolston, Mark Farrell, David T. Welsh, Justin D. Brookes, Alan S. Collins, Chris Keneally, and Juraj Farka

Cell-derived extracellular vesicles can be used as a biomarker reservoir for glioblastoma tumor subtyping

Glioblastoma (GBM) is one of the most aggressive solid tumors for which treatment options and biomarkers are limited. Small extracellular vesicles (sEVs) produced by both GBM and stromal cells are central in the inter-cellular communication that is taking place in the tumor bulk. As tumor sEVs are accessible in biofluids, recent reports have suggested that sEVs contain valuable biomarkers for GBM patient diagnosis and follow-up. The aim of the current study was to describe the protein content of sEVs produced by different GBM cell lines and patient-derived stem cells. Our results reveal that the content of the sEVs mirrors the phenotypic signature of the respective GBM cells, leading to the description of potential informative sEV-associated biomarkers for GBM subtyping, such as CD44. Overall, these data could assist future GBM in vitro studies and provide insights for the development of new diagnostic and therapeutic methods as well as personalized treatment strategies

Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome:phenotype comparison in two related syndromes

Background Ultrarare Marshall-Smith and Malan syndromes, caused by changes of the gene nuclear factor I X (NFIX), are characterised by intellectual disability (ID) and behavioural problems, although questions remain. Here, development and behaviour are studied and compared in a cross-sectional study, and results are presented with genetic findings. Methods Behavioural phenotypes are compared of eight individuals with Marshall-Smith syndrome (three male individuals) and seven with Malan syndrome (four male individuals). Long-term follow-up assessment of cognition and adaptive behaviour was possible in three individuals with Marshall-Smith syndrome. Results Marshall-Smith syndrome individuals have more severe ID, less adaptive behaviour, more impaired speech and less reciprocal interaction compared with individuals with Malan syndrome. Sensory processing difficulties occur in both syndromes. Follow-up measurement of cognition and adaptive behaviour in Marshall-Smith syndrome shows different individual learning curves over time. Conclusions Results show significant between and within syndrome variability. DifferentNFIXvariants underlie distinct clinical phenotypes leading to separate entities. Cognitive, adaptive and sensory impairments are common in both syndromes and increase the risk of challenging behaviour. This study highlights the value of considering behaviour within developmental and environmental context. To improve quality of life, adaptations to environment and treatment are suggested to create a better person-environment fit

Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848

Neurofibromatosis type 1 (NF1), a common genetic disorder with a birth incidence of 1:2,000–3,000, is characterized by a highly variable clinical presentation. To date, only two clinically relevant intragenic genotype-phenotype correlations have been reported for NF1 missense mutations affecting p.Arg1809 and a single amino acid deletion p.Met922del. Both variants predispose to a distinct mild NF1 phenotype with neither externally visible cutaneous/plexiform neurofibromas nor other tumors. Here, we report 162 individuals (129 unrelated probands and 33 affected relatives) heterozygous for a constitutional missense mutation affecting one of five neighboring NF1 codons—Leu844, Cys845, Ala846, Leu847, and Gly848—located in the cysteine-serine-rich domain (CSRD). Collectively, these recurrent missense mutations affect ∼0.8% of unrelated NF1 mutation-positive probands in the University of Alabama at Birmingham (UAB) cohort. Major superficial plexiform neurofibromas and symptomatic spinal neurofibromas were more prevalent in these individuals compared with classic NF1-affected cohorts (both p < 0.0001). Nearly half of the individuals had symptomatic or asymptomatic optic pathway gliomas and/or skeletal abnormalities. Additionally, variants in this region seem to confer a high predisposition to develop malignancies compared with the general NF1-affected population (p = 0.0061). Our results demonstrate that these NF1 missense mutations, although located outside the GAP-related domain, may be an important risk factor for a severe presentation. A genotype-phenotype correlation at the NF1 region 844–848 exists and will be valuable in the management and genetic counseling of a significant number of individuals