Computational fluid dynamics as a tool for urban drainage system analysis: a review of applications and best practice

Computational Fluid Dynamics (CFD) can be applied to gain insights into most fluid processes and associated phenomena and so presents potential to add value in the analysis of urban drainage systems. This paper presents a review of CFD studies carried out in this field, with the objective of developing an appreciation of how and where it can be applied. Existing work has tended to focus around the analysis of four types of urban drainage structure, including Combined Sewer Overflows (CSOs), storage and attenuation systems, stormwater sediment interceptors and sewerage conveyance structures. Within the respective studies, the prediction of flowfields, particulate behaviour, water surface profiles and Residence Time Distributions (RTDs) are found to form the main focus, and as such, these are considered in most detail in the paper. It is concluded that CFD presents a number of opportunities in urban drainage system analysis, and that the scope of this opportunity will further develop as both computational hardware and software resources become more advanced

Reducing the Risk of Invasive Pathogens to Wildlife Health in the United States

Call to Action In keeping with action items 4.3.1 and 4.3.2 of the 2016–2018 National Invasive Species Council (NISC) Management Plan, the Wildlife Health Task Team of the Invasive Species Advisory Committee (ISAC) was charged with: 1) identifying the major areas of vulnerability to native wildlife from the introduction and spread of invasive pathogens, and 2) making recommendations to address these vulnerabilities, including through potential changes in statute, regulation, policy, or practice of the relevant agencies

The cluster-scale AGN outburst in Hydra A

Deep Chandra observations of the Hydra A Cluster reveal a feature in the X-ray surface brightness that surrounds the 330 MHz radio lobes of the AGN at the cluster center. Surface brightness profiles of this feature and its close association with the radio lobes argue strongly that it is a shock front driven by the expanding radio lobes. The Chandra image also reveals other new structure on smaller scales that is associated with the radio source, including a large cavity and filament. The shock front extends 200 - 300 kpc from the AGN at the cluster center and its strength varies along the front, with Mach numbers in the range ~ 1.2 - 1.4. It is stronger where it is more distant from the cluster center, as expected for a shock driven by expanding radio lobes. Simple modeling gives an age for the shock front ~ 1.4\times10^8 y and a total energy driving it of ~ 10^{61} erg. The mean mechanical power driving the shock is comparable to quasar luminosities, well in excess of that needed to regulate the cooling core in Hydra A. This suggests that the feedback regulating cooling cores is inefficient, in that the bulk of the energy is deposited beyond the cooling core. In that case, a significant part of cluster "preheating" is a byproduct of the regulation of cooling cores.Comment: 7 pages, 6 figures, submitted to Ap

A High Resolution Study of the Hydra A Cluster with Chandra: Comparison of the Core Mass Distribution with Theoretical Predictions and Evidence for Feedback in the Cooling Flow

The cooling flow cluster Hydra A was observed during the orbital activation and calibration phase of the Chandra Observatory. While the X-ray image of the cluster exhibits complex structure in the central region as reported in McNamara $etal$, the large scale X-ray morphology of the cluster is fairly smooth. A spectroscopic analysis of the ACIS data shows that the gas temperature in Hydra A increases outward, reaches a maximum temperature of 4 keV at 200 kpc, and then decreases slightly at larger radii. The distribution of heavy elements is nonuniform, with a factor of two increase in the Fe and Si abundances within the central 100 kpc. Beyond the central 100 kpc the Si-to-Fe abundance ratio is twice solar, while the Si-to-Fe ratio of the central excess is consistent with the solar value. One of the more surprising results is the lack of spectroscopic evidence for multiphase gas within the bulk of the cooling flow. Beyond the central 30 kpc, the ACIS spectra are adequately fit with a single temperature model. The addition of a cooling flow component does not significantly improve the fit. Only within the central 30 kpc (where the cooling time is less than 1~Gyr), is there spectroscopic evidence for multiphase gas. However, the spectroscopic mass deposition rate is more than a factor of 10 less than the morphologically derived mass accretion rate at 30 kpc. We propose that the cooling flow region is convectively unstable due to heating by the central radio source which significantly reduces the net accretion rate.Comment: 19 figures include

Platelet activation independent of pulmonary inflammation contributes to diesel exhaust particulate-induced promotion of arterial thrombosis

BACKGROUND: Accelerated thrombus formation induced by exposure to combustion-derived air pollution has been linked to alterations in endogenous fibrinolysis and platelet activation in response to pulmonary and systemic inflammation. We hypothesised that mechanisms independent of inflammation contribute to accelerated thrombus formation following exposure to diesel exhaust particles (DEP). METHODS: Thrombosis in rats was assessed 2, 6 and 24 h after administration of DEP, carbon black (CB; control carbon nanoparticle), DQ12 quartz microparticles (to induce pulmonary inflammation) or saline (vehicle) by either intra-tracheal instillation (0.5 mg, except Quartz; 0.125 mg) or intravenous injection (0.5 mg/kg). Thrombogenicity was assessed by carotid artery occlusion, fibrinolytic variables and platelet-monocyte aggregates. Measures of inflammation were determined in plasma and bronchoalveolar lavage fluid. Tissue plasminogen activator (t-PA) and plasminogen activator inhibitor (PAI)-1 were measured following direct in vitro exposure of human umbilical vein endothelial cells (HUVECs) to DEP (10–150 μg/mL). RESULTS: Instillation of DEP reduced the time to thrombotic occlusion in vivo, coinciding with the peak of DEP-induced pulmonary inflammation (6 h). CB and DQ12 produced greater inflammation than DEP but did not alter time to thrombotic occlusion. Intravenous DEP produced an earlier (2 h) acceleration of thrombosis (as did CB) without pulmonary or systemic inflammation. DEP inhibited t-PA and PAI-1 release from HUVECs, and reduced the t-PA/PAI-1 ratio in vivo; similar effects in vivo were seen with CB and DQ12. DEP, but not CB or DQ12, increased platelet-monocyte aggregates. CONCLUSION: DEP accelerates arterial thrombus formation through increased platelet activation. This effect is dissociated from pulmonary and systemic inflammation and from impaired fibrinolytic function. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12989-016-0116-x) contains supplementary material, which is available to authorized users

Diabetes status and post-load plasma glucose concentration in relation to site-specific cancer mortality: findings from the original Whitehall study

ObjectiveWhile several studies have reported on the relation of diabetes status with pancreatic cancer risk, the predictive value of this disorder for other malignancies is unclear. Methods: The Whitehall study, a 25year follow-up for mortality experience of 18,006 men with data on post-challenge blood glucose and self-reported diabetes, allowed us to address these issues. Results: There were 2158 cancer deaths at follow-up. Of the 15 cancer outcomes, diabetes status was positively associated with mortality from carcinoma of the pancreas and liver, while the relationship with lung cancer was inverse, after controlling for a range of potential covariates and mediators which included obesity and socioeconomic position. After excluding deaths occurring in the first 10years of follow-up to examine the effect of reverse causality, the magnitude of the relationships for carcinoma of the pancreas and lung was little altered, while for liver cancer it was markedly attenuated. Conclusions: In the present study, diabetes status was related to pancreatic, liver, and lung cancer risk. Cohorts with serially collected data on blood glucose and covariates are required to further examine this area

Chaotic systems in complex phase space

This paper examines numerically the complex classical trajectories of the kicked rotor and the double pendulum. Both of these systems exhibit a transition to chaos, and this feature is studied in complex phase space. Additionally, it is shown that the short-time and long-time behaviors of these two PT-symmetric dynamical models in complex phase space exhibit strong qualitative similarities.Comment: 22 page, 16 figure

Global Molecular Epidemiology of Respiratory Syncytial Virus from the 2017-2018 INFORM-RSV Study

Respiratory syncytial virus (RSV) is the leading cause of lower respiratory tract infection among infants and young children, resulting in annual epidemics worldwide. INFORM-RSV is a multiyear clinical study designed to describe the global molecular epidemiology of RSV in children under 5 years of age by monitoring temporal and geographical evolution of current circulating RSV strains, F protein antigenic sites, and their relationships with clinical features of RSV disease. During the pilot season (2017-2018), 410 RSV G-F gene sequences were obtained from 476 RSV-positive nasal samples collected from 8 countries (United Kingdom, Spain, The Netherlands, Finland, Japan, Brazil, South Africa, and Australia). RSV B (all BA9 genotype) predominated over RSV A (all ON1 genotype) globally (69.0% versus 31.0%) and in all countries except South Africa. Geographic clustering patterns highlighted wide transmission and continued evolution with viral spread. Most RSV strains were from infants of 24 h (70.5%), with no differences in subtype distribution. Compared to 2013 reference sequences, variations at F protein antigenic sites were observed for both RSV A and B strains, with high-frequency polymorphisms at antigenic site Ø (I206M/Q209R) and site V (L172Q/S173L/K191R) in RSV B strains. The INFORM-RSV 2017-2018 pilot season establishes an important molecular baseline of RSV strain distribution and sequence variability with which to track the emergence of new strains and provide an early warning system of neutralization escape variants that may impact transmission or the effectiveness of vaccines and MAbs under development

Finishing a whole-genome shotgun: Release 3 of the Drosophila melanogaster euchromatic genome sequence

BACKGROUND: The Drosophila melanogaster genome was the first metazoan genome to have been sequenced by the whole-genome shotgun (WGS) method. Two issues relating to this achievement were widely debated in the genomics community: how correct is the sequence with respect to base-pair (bp) accuracy and frequency of assembly errors? And, how difficult is it to bring a WGS sequence to the accepted standard for finished sequence? We are now in a position to answer these questions. RESULTS: Our finishing process was designed to close gaps, improve sequence quality and validate the assembly. Sequence traces derived from the WGS and draft sequencing of individual bacterial artificial chromosomes (BACs) were assembled into BAC-sized segments. These segments were brought to high quality, and then joined to constitute the sequence of each chromosome arm. Overall assembly was verified by comparison to a physical map of fingerprinted BAC clones. In the current version of the 116.9 Mb euchromatic genome, called Release 3, the six euchromatic chromosome arms are represented by 13 scaffolds with a total of 37 sequence gaps. We compared Release 3 to Release 2; in autosomal regions of unique sequence, the error rate of Release 2 was one in 20,000 bp. CONCLUSIONS: The WGS strategy can efficiently produce a high-quality sequence of a metazoan genome while generating the reagents required for sequence finishing. However, the initial method of repeat assembly was flawed. The sequence we report here, Release 3, is a reliable resource for molecular genetic experimentation and computational analysis