Interaction between the intergalactic medium and central radio source in the NGC 4261 group of galaxies

Using observations from the Chandra and XMM-Newton X-ray observatories, we examine the interaction between the intra-group medium and central radio source in the nearby NGC 4261 galaxy group. We confirm the presence of cavities associated with the radio lobes and estimate their enthalpy to be ~2.4x10^58 erg. The mechanical power output of the jets is >=10^43 erg/s, at least a factor of 60 greater than the cooling luminosity in the region the lobes inhabit. We identify rims of compressed gas enclosing the lobes, but find no statistically significant temperature difference between them and their surroundings, suggesting that the lobe expansion velocity is approximately sonic (Mach<=1.05). The apparent pressure of the radio lobes, based on the synchrotron minimum energy density argument, is a factor of 5 lower than that of the intra-group medium. Pressure balance could be achieved if entrainment of thermal gas provided additional non-radiating particles in the lobe plasma, but the energy required to heat these particles would be ~20 per cent. of the mechanical energy output of the radio source. NGC 4261 has a relatively compact cool core, which should probably be categorised as a galactic corona. The corona is capable of fuelling the active nucleus for considerably longer than the inferred source lifetime, but can be only inefficiently heated by the AGN or conduction. The expansion of the radio lobes has affected the structure of the gas in the galaxy, compressing and moving the material of the corona without causing significant shock heating, and expelling gas from the immediate neighbourhood of the jets. We discuss the possible implications of this environment for the duration of the AGN outburst, and consider mechanisms which might lead to the cessation of nuclear activity.Comment: Accepted for publication in MNRAS, 17 pages, 6 figure

What treatments relieve painful heel cracks?

Emollient cream may alleviate pain and dryness and improve the appearance of heel cracks (strength of recommendation [SOR]: B, one small randomized trial). Foot soaks followed by mechanical debridement and topical petrolatum may decrease the depth of cracks and thickness of calluses in patients with leprosy (SOR: C, 1 small cohort study). Keratolytic agents, such as salicylic acid, may reduce hyperkeratosis, cracks, and pain (SOR: C, one case-control study). Cyanoacrylate tissue adhesives, such as Superglue or Krazy Glue, may reduce pain and speed closure of heel cracks (SOR: C, one case series). Maintenance therapy with emollients and appropriate footwear also may help heel cracks (SOR: C, expert opinion)

Detecting harmful algal blooms with isothermal molecular strategies

The use of isothermal nucleic acid amplification strategies to detect harmful algal blooms (HABs) is in its infancy. We describe recent advances in these systems and highlight the challenges for the achievement of simple, low-cost, compact, and portable devices for field applications.info:eu-repo/semantics/acceptedVersio

Egg Shell Quality Assessment–Do We Need Multiple Records?

The objective of this study was to estimate repeatability within and between ages for dynamic stiffnessin two lines of layer chickens in order to verify if multiple records are necessary to adequately describe a bird’s genetic merit for egg shell quality.Repeatability was low across ages to moderate within age,which suggests that for accurate evaluation eggs should be collected at different stages of laying cycle,with additional benefit from analyzing more than one egg within age

Evaluation of Egg Production in Layers Using Random Regression Models

The objectives of this study were to estimate genetic parameters for egg production over the age trajectory in three commercial layer breeding lines, which represent different biotypes for egg production, and to validate the use of breeding values for slope as a measure of persistency to be used in the selection program. Egg production data of over 26,000 layers per line from six consecutive generations were analyzed. Daily records were cumulated into biweekly periods. Data were analyzed with a random regression model with linear polynomials on period for random additive genetic and permanent environmental effects. In all lines, a nonzero genetic variance for mean and slope and a positive genetic correlation between mean and slope were estimated. Breeding values for slope well reflected the shape of the egg production curve and can be used to select for persistency of egg production. The model proposed in this study appealing for implementation in large and multiple populations under commercial conditions by breeding companies or other breeding organizations

Detection of isothermally amplified ostreid herpesvirus 1 DNA in Pacific oyster (Crassostrea gigas) using a miniaturised electrochemical biosensor

Given the threat that ostreid herpesvirus 1 (OsHV-1) poses to shellfish aquaculture, the need for rapid, user-friendly and cost-effective methods to detect this marine pathogen and minimise its impact is evident. In this work, an electrochemical biosensor for the detection of OsHV-1 based on isothermal recombinase polymerase amplification (RPA) was developed. The system was first tested and optimised on maleimide microtitre plates as a proof-of-concept, before being implemented on miniaturised gold electrodes. Amperometric detection of the isothermally amplified product was achieved through a sandwich hybridisation assay with an immobilised thiolated capture probe and a horseradish peroxidase (HRP)-labelled reporter probe. Calibration curves were constructed using PCR-amplified OsHV-1 DNA, achieving a limit of detection of 207 OsHV-1 target copies. The biosensor was applied to the analysis of 16 oyster samples from an infectivity experiment, and results were compared with those obtained by qPCR analysis, showing a strong degree of correlation (r = 0.988). The simplicity, rapidity, cost-effectiveness and potential for in-situ testing with the developed biosensor provide a valuable tool for the detection of OsHV-1 in aquaculture facilities, improving their management.info:eu-repo/semantics/acceptedVersio

Detection of Ostreopsis cf. ovata in environmental samples using an electrochemical DNA-based biosensor

Ostreopsis cf. ovata is a benthic microalga distributed in tropical and temperate regions worldwide which produces palytoxins (PlTXs). Herein, an electrochemical biosensor for the detection of this toxic microalga is described. The detection strategy involves isothermal recombinase polymerase amplification (RPA) of the target using tailed primers and a sandwich hybridisation assay on maleimide-coated magnetic beads immobilised on electrode arrays. The biosensor attained a limit of detection of 9 pg/μL of O. cf. ovata DNA (which corresponds to ~640 cells/L), with no interferences from two non-target Ostreopsis species (O. cf. siamensis and O. fattorussoi). The biosensor was applied to the analysis of planktonic and benthic environmental samples. Electrochemical O. cf. ovata DNA quantifications demonstrated an excellent correlation with other molecular methods (qPCR and colorimetric assays) and allowed the construction of a predictive regression model to estimate O. cf. ovata cell abundances. This new technology offer great potential to improve research, monitoring and management of O. cf. ovata and harmful algal blooms.info:eu-repo/semantics/acceptedVersio

Evaluation of Claviceps purpurea isolates on wheat reveals complex virulence and host susceptibility relationships

Ergot of cereals, caused by Claviceps purpurea, results in yield loss and downgrading of infested grain because of toxic alkaloids in the sclerotia. Resistant wheat genotypes are known, but their effectiveness against different C. purpurea isolates over geographic regions has not been studied. The objective of this study was to examine the pathogenic variability among isolates of C. purpurea on wheat lines differing in resistance. Under controlled environmental conditions, 41 single spore isolates of C. purpurea were obtained from Canadian and UK collections and inoculated onto a set of wheat genotypes composed of durum wheat lines ‘Melita’, ‘Kyle’ and 9260B-173A, and hexaploid spring wheat lines ‘Cadillac’, ‘Vista’, ‘Kenya Farmer’, ‘Lee’ and HY630. Honeydew production and weight of sclerotia produced per spike were assessed. There were significant differences among the wheat genotypes for overall reactions to the pathogen isolates, and among pathogen isolates for geographic origin and host origin. Twenty virulence phenotypes were identified using the honeydew production data, and 23 virulence phenotypes identified using the sclerotial weight data from the 41 isolates. The existence of different virulence phenotypes indicates that variability in virulence exists in populations of C. purpurea, and knowledge of virulence phenotypes is necessary to effectively breed for resistant commercial lines

Electrochemical genosensor for the direct detection of tailed PCR amplicons incorporating ferrocene labelled dATP

An electrochemical genosensor for the detection and quantification of Karlodinium armiger is presented. The genosensor exploits tailed primers and ferrocene labelled dATP analogue to produce PCR products that can be directly hybridised on a gold electrode array and quantitatively measured using square wave voltammetry. Tailed primers consist of a sequence specific for the target, followed by a carbon spacer and a sequence specifically designed not to bind to genomic DNA, resulting in a duplex flanked by single stranded binding primers. The incorporation of the 7-(ferrocenylethynyl)-7-deaza-2′-deoxyadenosine triphosphate was optimised in terms of a compromise between maximum PCR efficiency and the limit of detection and sensitivity attainable using electrochemical detection via hybridisation of the tailed, ferrocene labelled PCR product. A limit of detection of 277aM with a linear range from 315aM to 10 fM starting DNA concentration and a sensitivity of 122 nA decade−1 was achieved. The system was successfully applied to the detection of genomic DNA in real seawater samples.info:eu-repo/semantics/acceptedVersio