323 research outputs found
Towards a greater understanding of the presence, fate and ecological effects of microplastics in the freshwater environment
This thesis combines field and laboratory studies to address some of the most pressing questions in the field of microplastic research. Specifically, the thesis addresses the topic of microplastics in the freshwater environment. The research presented covers both the environmental presence and abundance of microplastics, in addition to ecological effects, investigated using observational and experimental studies. These studies give a greater understanding of the abundance, types and sources of microplastics in freshwater systems in the UK, how organisms and chemicals interact with microplastics and the potential ecological effects on a range of freshwater organisms from different functional feeding groups and trophic levels.Environmental Biolog
Viral antibody dynamics in a chiropteran host
1. Bats host many viruses that are significant for human and domestic animal health, but the dynamics of these infections in their natural reservoir hosts remain poorly elucidated.<p></p>
2. In these, and other, systems, there is evidence that seasonal life-cycle events drive infection dynamics, directly impacting the risk of exposure to spillover hosts. Understanding these dynamics improves our ability to predict zoonotic spillover from the reservoir hosts.<p></p>
3. To this end, we followed henipavirus antibody levels of >100 individual E. helvum in a closed, captive, breeding population over a 30-month period, using a powerful novel antibody quantitation method.<p></p>
4. We demonstrate the presence of maternal antibodies in this system and accurately determine their longevity. We also present evidence of population-level persistence of viral infection and demonstrate periods of increased horizontal virus transmission associated with the pregnancy/lactation period.<p></p>
5.The novel findings of infection persistence and the effect of pregnancy on viral transmission, as well as an accurate quantitation of chiropteran maternal antiviral antibody half-life, provide fundamental baseline data for the continued study of viral infections in these important reservoir hosts
Identifying Cancer Specific Metabolic Signatures Using Constraint-Based Models
Cancer metabolism differs remarkably from the metabolism of healthy surrounding tissues, and it is extremely heterogeneous across cancer types. While these metabolic differences provide promising avenues for cancer treatments, much work remains to be done in understanding how metabolism is rewired in malignant tissues. To that end, constraint-based models provide a powerful computational tool for the study of metabolism at the genome scale. To generate meaningful predictions, however, these generalized human models must first be tailored for specific cell or tissue sub-types. Here we first present two improved algorithms for (1) the generation of these context-specific metabolic models based on omics data, and (2) Monte-Carlo sampling of the metabolic model ux space. By applying these methods to generate and analyze context-specific metabolic models of diverse solid cancer cell line data, and primary leukemia pediatric patient biopsies, we demonstrate how the methodology presented in this study can generate insights into the rewiring differences across solid tumors and blood cancers
Extending standard testing period in honeybees to predict lifespan impacts of pesticides and heavy metals using dynamic energy budget modelling
Concern over reported honeybee (Apis mellifera spp.) losses has highlighted chemical exposure as a risk. Current laboratory oral toxicity tests in A. mellifera spp. use short-term, maximum 96 hour, exposures which may not necessarily account for chronic and cumulative toxicity. Here, we use extended 240 hour (10 day) exposures to examine seven agrochemicals and trace environmental pollutant toxicities for adult honeybees. Data were used to parameterise a dynamic energy budget model (DEBtox) to further examine potential survival effects up to 30 day and 90 day summer and winter worker lifespans. Honeybees were most sensitive to insecticides (clothianidin > dimethoate ≫ tau-fluvalinate), then trace metals/metalloids (cadmium, arsenic), followed by the fungicide propiconazole and herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). LC50s calculated from DEBtox parameters indicated a 27 fold change comparing exposure from 48 to 720 hours (summer worker lifespan) for cadmium, as the most time-dependent chemical as driven by slow toxicokinetics. Clothianidin and dimethoate exhibited more rapid toxicokinetics with 48 to 720 hour LC50s changes of <4 fold. As effects from long-term exposure may exceed those measured in short-term tests, future regulatory tests should extend to 96 hours as standard, with extension to 240 hour exposures further improving realism
2-(1,3-Benzothiazol-2-yl)guanidinium chloride
The non-H atoms of the cation of the title salt, C8H9N4S+·Cl−, are approximately co-planar (r.m.s. deviation = 0.037 Å), with one amino group forming an intramolecular hydrogen bond to the tertiary N atom of the benzothiazole fused-ring system. The cations and anions are linked by cyclic R
2
1(6) N—H⋯Cl hydrogen-bonding associations, generating helical chains running along the b-axis direction
Temperature dependence of single particle excitations in a S=1 chain: exact diagonalization calculations compared to neutron scattering experiments
Exact diagonalization calculations of finite antiferromagnetic spin-1
Heisenberg chains at finite temperatures are presented and compared to a recent
inelastic neutron scattering experiment for temperatures T up to 7.5 times the
intrachain exchange constant J. The calculations show that the excitations at
the antiferromagnetic point q=1 and at q=0.5 remain resonant up to at least
T=2J, confirming the recent experimental observation of resonant
high-temperature domain wall excitations. The predicted first and second
moments are in good agreement with experiment, except at temperatures where
three-dimensional spin correlations are most important. The ratio of the
structure factors at q=1 and at q=0.5 is well predicted for the paramagnetic
infinite-temperature limit. For T=2J, however, we found that the experimentally
observed intensity is considerably less than predicted. This suggests that
domain wall excitations on different chains interact up to temperatures of the
order of the spin band width.Comment: 9 pages revtex, submitted to PR
2-(1,3-Benzoxazol-2-yl)guanidinium chloride
The non-H atoms of the cation of the title salt, C8H9N4O+·Cl−, are approximately co-planar (r.m.s. deviation = 0.024 Å) with one amino group forming an intramolecular hydrogen bond to the tertiary N atom of the benzoxazole fused-ring system. The cations and anions are linked by cyclic R
2
1(6) N—H⋯Cl hydrogen-bonding associations, generating linear chains running along the a-axis direction
Syntheses, X-ray structures and characterisation of luminescent chromium(III) complexes incorporating 8-quinolinato ligands
A series of six coordinate homoleptic and heteroleptic Cr(III) complexes have been formed that incorporate 8-quinolinato ligands. Three classes of complex have been synthesised and characterised: (i) [Cr(Q)3]; (ii) [Cr(Q)2(H2O)2]Cl; (iii) [Cr(Q)(N^N)2](PF6)2 (where Q is a ligand, 8-hydroxyquinoline, 8-hydroxy-2-methyl-quinoline, or 8-hydroxy-5-nitroquinoline; N^N = 1,10-phenanthroline or 2,2′-bipyridine). Single crystal X-ray structures were obtained for four complexes giving examples of [Cr(Q)2(H2O)2]Cl, two [Cr(Q)(bipy)2](PF6)2 and [Cr(Q)(phen)2](PF6)2. Each complex shows the ligands in the expected coordination mode with a distorted octahedral geometry evident at the metal centre. The UV–Vis. absorption data allowed assignments of the quinolinato-centred electronic transitions together with a much weaker spin allowed d–d transition (4A2 → 4T2) around 550 nm. Each complex was found to be luminescent in aerated MeCN solution at room temperature, which was attributed to a ligand-centred fluorescence based on the coordinated quinolinato ligand
Magnetoluminescence
Pulsar Wind Nebulae, Blazars, Gamma Ray Bursts and Magnetars all contain
regions where the electromagnetic energy density greatly exceeds the plasma
energy density. These sources exhibit dramatic flaring activity where the
electromagnetic energy distributed over large volumes, appears to be converted
efficiently into high energy particles and gamma-rays. We call this general
process magnetoluminescence. Global requirements on the underlying, extreme
particle acceleration processes are described and the likely importance of
relativistic beaming in enhancing the observed radiation from a flare is
emphasized. Recent research on fluid descriptions of unstable electromagnetic
configurations are summarized and progress on the associated kinetic
simulations that are needed to account for the acceleration and radiation is
discussed. Future observational, simulation and experimental opportunities are
briefly summarized.Comment: To appear in "Jets and Winds in Pulsar Wind Nebulae, Gamma-ray Bursts
and Blazars: Physics of Extreme Energy Release" of the Space Science Reviews
serie
Experimental Lagos bat virus infection in straw-colored fruit bats: A suitable model for bat rabies in a natural reservoir species
Rabies is a fatal neurologic disease caused by lyssavirus infection. Bats are important natural reservoir hosts of various lyssaviruses that can be transmitted to people. The epidemiology and pathogenesis of rabies in bats are poorly understood, making it difficult to prevent zoonotic transmission. To further our understanding of lyssavirus pathogenesis in a natural bat host, an experimental model using straw-colored fruit bats (Eidolon helvum) and Lagos bat virus, an endemic lyssavirus in this species, was developed. To determine the lowest viral dose resulting in 100% productive infection, bats in five groups (four bats per group) were inoculated intramuscularly with one of five doses, ranging from 100.1 to 104.1 median tissue culture infectious dose (TCID50). More bats died due to the development of rabies after the middle dose (102.1 TCID50, 4/4 bats) than after lower (101.1, 2/4; 101.1, 2/4) or higher (103.1, 2/4; 104.1, 2/4) doses of virus. In the two highest dose groups, 4/8 bats developed rabies. Of those bats that remained healthy 3/4 bats seroconverted, suggesting that high antigen loads can trigger a strong immune response that abrogates a productive infection. In contrast, in the two lowest dose groups, 3/8 bats developed rabies, 1/8 remained healthy and seroconverted and 4/8 bats remained healthy and did not seroconvert, suggesting these doses are too low to reliably induce infection. The main lesion in all clinically affected bats was meningoencephalitis associated with lyssavirus-positive neurons. Lyssavirus antigen was detected in tongue epithelium (5/11 infected bats) rather than in salivary gland epithelium (0/11), suggesting viral excretion via the tongue. Thus, intramuscular inoculation of 102.1 TCID50 of Lagos bat virus into straw-colored fruit bats is a suitable m
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