959 research outputs found
Spatial and Habitat Responses of Canada Lynx in Maine to a Decline in Snowshoe Hare Density
Previous studies of Canada lynx (Lynx canadensis) within the northern boreal forest region have documented that lynx respond spatially to a decline in snowshoe hare (Lepus americanus) density, as exhibited by expansion of territories and changes in social structure. I compared home range area and spatial overlap in the southeastern portion of their geographic range during periods of relatively high and relatively low hare density. Home range areas of lynx did not change between periods of high and low hare density, except that home ranges of females during the denning season expanded during the low period. The presence of kittens constrained home range areas of reproductive females during denning because females were attending kittens. Intra- and intersexual overlap did not change as hare density declined, with the exception of a decrease in overlap between females. This decrease was likely caused by decreased reproduction during the low period, which reduced potential for territorial overlap among mothers and daughters. Hare density during the nadir of cycles in more northerly populations can reach levels nearly a magnitude lower than reported for Maine during my study. This may have prevented breakdowns in territories and changes in social structure by lynx, which may have shifted life history strategies towards territorial maintenance and reduced reproduction as hare densities declined.
I also investigated changes in use of high-quality hare habitat (HQHH) at the landscape scale, and habitat selection of HQHH within home ranges of lynx between periods of high and low hare density. Lynx did not change their extent of use of HQHH at the landscape scale, suggesting lynx had adequate amounts of HQHH within their home ranges to encounter hares during both the high and low periods of hare density. Lynx exhibited stand-scale selection for HQHH during both hare density periods, but the intensity of female selection for HQHH declined as hare density declined. This suggests that lynx continued to remain focused on foraging for hares during both periods, but that females may become more generalized in habitat and prey selection during the period of lower hare density.
Lynx monitored during this study wore GPS collars during a period of low hare density and VHF collars during a period of high hare density. This presented methodological challenges when I compared lynx responses between hare density periods. Errors associated with VHF collars were known for this study, but errors associated with GPS collars were not. Failed fix attempts and location inaccuracy caused by environmental and satellite configurations can bias habitat selection and spatial analyses. I evaluated fix success and location error of GPS collars in 7 habitat classes during 2 seasons in northern Maine. I also used an information-theoretic modeling approach to investigate covariates influencing fix success and location error. Canopy cover had the greatest influence on fix success and the configuration of available satellites had the greatest influence on location error. Results were used to compensate for habitat bias and location error caused by GPS collars worn by lynx during a period of low hare density
The incidence and position of melanocytic nevi for the purposes of forensic image comparison
Expert witness opinion based on the comparison of images has been accepted by UK courts as admissible evidence in relation to issues of identity. Within images of the hand are a multiplicity of anatomical features of different aetiology, incidence and distribution patterns and this includes melanocytic nevi, referred to more colloquially as moles and/or birthmarks. The hand is not a common place for these isolated features to develop and so their presence in this anatomical region has the potential to be useful for issues of identity. The results of this study show that approximately 9 % of individuals in a sample of 476 hands, displayed at least one nevus on the back of their hand and, contrary to the literature, the incidence was found to be greater in females (15 % of female cohort) than males (7 % of male cohort). Almost a third of all nevi identified on the dorsum of the hand were abnormal or dysplastic. The most frequent location for these aggregations of melanocytes was in the central region of the dorsum of the hand or at the base of the index finger. The relevance of nevi identified in the image of a perpetrator’s hand and also on that of a suspect/accused is discussed in relation to the issue of whether the images have originated from the same individual
Muon-spin-rotation study of the magnetic structure in the tetragonal antiferromagnetic state of weakly underdoped BaKFeAs
With muon spin rotation (SR) we studied the transition between the
orthorhombic antiferromagnetic (o-AF) and the tetragonal antiferromagnetic
(t-AF) states of a weakly underdoped BaKFeAs
single crystal. We observed some characteristic changes of the magnitude and
the orientation of the magnetic field at the muon site which, due to the fairly
high point symmetry of the latter, allow us to identify the magnetic structure
of the t-AF state. It is the so-called, inhomogeneous double-
magnetic structure with -axis oriented moments which has a vanishing
magnetic moment on half of the Fe sites.Comment: 5 pages, 4 figures. Supplementary Material: 8 figure
Predicting risk of osteoporotic and hip fracture in the United Kingdom: prospective independent and external validation of QFractureScores
Objective To evaluate the performance of the QFractureScores for predicting the 10 year risk of osteoporotic and hip fractures in an independent UK cohort of patients from general practice records
Reporting of prognostic studies of tumour markers: a review of published articles in relation to REMARK guidelines
Background: Poor reporting compromises the reliability and clinical value of prognostic tumour marker studies. We review articles to assess the reporting of patients and events using REMARK guidelines, at the time of guideline publication. Methods: We sampled 50 prognostic tumour marker studies from higher impact cancer journals between 2006 and 2007. The inclusion criteria were cancer; focus on single biological tumour marker; survival analysis; multivariable analysis; and not gene array or proteomic data. Articles were assessed for the REMARK profile and other REMARK guideline items. We propose a reporting aid, the REMARK profile, motivated by the CONSORT flowchart. Results: In 50 studies assessed for the REMARK profile, the number of eligible patients (56% of articles), excluded patients (54%) and patients in analyses (98%) was reported. Only 50% of articles reported the number of outcome events. In multivariable analyses, 54% and 30% of articles reported patient and event numbers for all variables. Of the studies, 66% used archival samples, indicating a potentially biased patient selection. Only 36% of studies reported clearly defined outcomes. Conclusions: Good reporting is critical for the interpretability and clinical applicability of prognostic studies. Current reporting of key information, such as the number of outcome events in all patients and subgroups, is poor. Use of the REMARK profile would greatly improve reporting and enhance prognostic research
Non-stationary rotating black holes: Entropy and Hawking's radiation
We derive a class of non-stationary embedded rotating black holes and study
the Hawking's radiation effects on these embedded black holes. The surface
gravity, entropy and angular velocity, which are three important properties of
black holes, are presented for each of these embedded black holes.Comment: 36 pages, LaTe
Reporting methods in studies developing prognostic models in cancer: a review
Development of prognostic models enables identification of variables that are influential in predicting patient outcome and the use of these multiple risk factors in a systematic, reproducible way according to evidence based methods. The reliability of models depends on informed use of statistical methods, in combination with prior knowledge of disease. We reviewed published articles to assess reporting and methods used to develop new prognostic models in cancer.We developed a systematic search string and identified articles from PubMed. Forty-seven articles were included that satisfied the following inclusion criteria: published in 2005; aiming to predict patient outcome; presenting new prognostic models in cancer with outcome time to an event and including a combination of at least two separate variables; and analysing data using multivariable analysis suitable for time to event data.In 47 studies, prospective cohort or randomised controlled trial data were used for model development in only 33% (15) of studies. In 30% (14) of the studies insufficient data were available, having fewer than 10 events per variable (EPV) used in model development. EPV could not be calculated in a further 40% (19) of the studies. The coding of candidate variables was only reported in 68% (32) of the studies. Although use of continuous variables was reported in all studies, only one article reported using recommended methods of retaining all these variables as continuous without categorisation. Statistical methods for selection of variables in the multivariate modelling were often flawed. A method that is not recommended, namely, using statistical significance in univariate analysis as a pre-screening test to select variables for inclusion in the multivariate model, was applied in 48% (21) of the studies.We found that published prognostic models are often characterised by both use of inappropriate methods for development of multivariable models and poor reporting. In addition, models are limited by the lack of studies based on prospective data of sufficient sample size to avoid overfitting. The use of poor methods compromises the reliability of prognostic models developed to provide objective probability estimates to complement clinical intuition of the physician and guidelines
Reporting performance of prognostic models in cancer: a review
<p>Abstract</p> <p>Background</p> <p>Appropriate choice and use of prognostic models in clinical practice require the use of good methods for both model development, and for developing prognostic indices and risk groups from the models. In order to assess reliability and generalizability for use, models need to have been validated and measures of model performance reported. We reviewed published articles to assess the methods and reporting used to develop and evaluate performance of prognostic indices and risk groups from prognostic models.</p> <p>Methods</p> <p>We developed a systematic search string and identified articles from PubMed. Forty-seven articles were included that satisfied the following inclusion criteria: published in 2005; aiming to predict patient outcome; presenting new prognostic models in cancer with outcome time to an event and including a combination of at least two separate variables; and analysing data using multivariable analysis suitable for time to event data.</p> <p>Results</p> <p>In 47 studies, Cox models were used in 94% (44), but the coefficients or hazard ratios for the variables in the final model were reported in only 72% (34). The reproducibility of the derived model was assessed in only 11% (5) of the articles. A prognostic index was developed from the model in 81% (38) of the articles, but researchers derived the prognostic index from the final prognostic model in only 34% (13) of the studies; different coefficients or variables from those in the final model were used in 50% (19) of models and the methods used were unclear in 16% (6) of the articles. Methods used to derive prognostic groups were also poor, with researchers not reporting the methods used in 39% (14 of 36) of the studies and data derived methods likely to bias estimates of differences between risk groups being used in 28% (10) of the studies. Validation of their models was reported in only 34% (16) of the studies. In 15 studies validation used data from the same population and in five studies from a different population. Including reports of validation with external data from publications up to four years following model development, external validation was attempted for only 21% (10) of models. Insufficient information was provided on the performance of models in terms of discrimination and calibration.</p> <p>Conclusions</p> <p>Many published prognostic models have been developed using poor methods and many with poor reporting, both of which compromise the reliability and clinical relevance of models, prognostic indices and risk groups derived from them.</p
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