5,690 research outputs found
Impact assessment framework to identify sustainable urban mobility solutions (EIT Urban Mobility Innovation Pathway Project - Final Report)
This report describes a new impact assessment framework to identify the policy solutions that enable cities to meet their vision and objectives, taking into account the local context. The framework was developed as a part of the EIT (European Institute of Innovation and Technology) Urban Mobility Innovation Pathway project. The framework consists of three groups of indicators, describing:
⢠the city-level context in which the policy measures are applied
⢠the characteristics of the process through which the policy measures are applied
⢠the likely outcomes and impacts of the policy measur
Oxidation of myoglobin in isolated adult rat cardiac myocytes by 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid
AbstractThe oxidation of intracellular myoglobin by 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid was studied in suspensions of isolated adult rat heart cells. Myoglobin was converted to a species identified as ferrylMb by its reaction with Na2S to form ferrous sulfmyoglobin. This process was time-dependent and concentration-dependent in a manner consistent with direct accessibility of the exogenous peroxide to the cytosolic protein. The results indicate that myoglobin oxidation may be an early sign of oxidative injury and may limit myocardial function by elimination of this short-term O2 reserve
Spatial sampling heterogeneity limits the detectability of deep time latitudinal biodiversity gradients
The latitudinal biodiversity gradient (LBG), in which species richness decreases from tropical to polar regions, is a pervasive pattern of the modern biosphere. Although the distribution of fossil occurrences suggests this pattern has varied through deep time, the recognition of palaeobiogeographic patterns is hampered by geological and anthropogenic biases. In particular, spatial sampling heterogeneity has the capacity to impact upon the reconstruction of deep time LBGs. Here we use a simulation framework to test the detectability of three different types of LBG (flat, unimodal and bimodal) over the last 300 Myr. We show that heterogeneity in spatial sampling significantly impacts upon the detectability of genuine LBGs, with known biodiversity patterns regularly obscured after applying the spatial sampling window of fossil collections. Sampling-standardization aids the reconstruction of relative biodiversity gradients, but cannot account for artefactual absences introduced by geological and anthropogenic biases. Therefore, we argue that some previous studies might have failed to recover the âtrueâ LBG type owing to incomplete and heterogeneous sampling, particularly between 200 and 20 Ma. Furthermore, these issues also have the potential to bias global estimates of past biodiversity, as well as inhibit the recognition of extinction and radiation events
The cysteine proteome
AbstractThe cysteine (Cys) proteome is a major component of the adaptive interface between the genome and the exposome. The thiol moiety of Cys undergoes a range of biologic modifications enabling biological switching of structure and reactivity. These biological modifications include sulfenylation and disulfide formation, formation of higher oxidation states, S-nitrosylation, persulfidation, metalation, and other modifications. Extensive knowledge about these systems and their compartmentalization now provides a foundation to develop advanced integrative models of Cys proteome regulation. In particular, detailed understanding of redox signaling pathways and sensing networks is becoming available to allow the discrimination of network structures. This research focuses attention on the need for atlases of Cys modifications to develop systems biology models. Such atlases will be especially useful for integrative studies linking the Cys proteome to imaging and other omics platforms, providing a basis for improved redox-based therapeutics. Thus, a framework is emerging to place the Cys proteome as a complement to the quantitative proteome in the omics continuum connecting the genome to the exposome
Drosophila OBP LUSH Is Required for Activity of Pheromone-Sensitive Neurons
AbstractOdorant binding proteins (OBPs) are extracellular proteins localized to the chemosensory systems of most terrestrial species. OBPs are expressed by nonneuronal cells and secreted into the fluid bathing olfactory neuron dendrites. Several members have been shown to interact directly with odorants, but the significance of this is not clear. We show that the Drosophila OBP lush is completely devoid of evoked activity to the pheromone 11-cis vaccenyl acetate (VA), revealing that this binding protein is absolutely required for activation of pheromone-sensitive chemosensory neurons. lush mutants are also defective for pheromone-evoked behavior. Importantly, we identify a genetic interaction between lush and spontaneous activity in VA-sensitive neurons in the absence of pheromone. The defects in spontaneous activity and VA sensitivity are reversed by germline transformation with a lush transgene or by introducing recombinant LUSH protein into mutant sensilla. These studies directly link pheromone-induced behavior with OBP-dependent activation of a subset of olfactory neurons
Short-term oral atrazine exposure alters the plasma metabolome of male C57BL/6 mice and disrupts Îą -linolenate, tryptophan, tyrosine and other major metabolic pathways
Overexposure to the commonly used herbicide atrazine (ATR) affects several organ systems, including the brain. Previously, we demonstrated that short-term oral ATR exposure causes behavioral deficits and dopaminergic and serotonergic dysfunction in the brains of mice. Using adult male C57BL/6 mice, the present study aimed to investigate effects of a 10-day oral ATR exposure (0, 5, 25, 125, or 250 mg/kg) on the mouse plasma metabolome and to determine metabolic pathways affected by ATR that may be reflective of ATRâs effects on the brain and useful to identify peripheral biomarkers of neurotoxicity. Four h after the last dosing on day 10, plasma was collected and analyzed with high-performance, dual chromatography-Fourier-transform mass spectrometry that was followed by biostatistical and bioinformatic analyses. ATR exposure (âĽ5 mg/kg) significantly altered plasma metabolite profile and resulted in a dose-dependent increase in the number of metabolites with ion intensities significantly different from the control group. Pathway analyses revealed that ATR exposure strongly correlated with and disrupted multiple metabolic pathways. Tyrosine, tryptophan, linoleic acid and Îą-linolenic acid metabolic pathways were among the affected pathways, with Îą-linolenic acid metabolism being affected to the greatest extent. Observed effects of ATR on plasma tyrosine and tryptophan metabolism may be reflective of the previously reported perturbations of brain dopamine and serotonin homeostasis, respectively. ATR-caused alterations in the plasma profile of Îą-linolenic acid metabolism are a potential novel and sensitive plasma biomarker of ATR effect and plasma metabolomics could be used to better assess the risks, including to the brain, associated with ATR overexposure
Field theoretic calculation of the surface tension for a model electrolyte system
We carry out the calculation of the surface tension for a model electrolyte
to first order in a cumulant expansion about a free field theory equivalent to
the Debye-H\"uckel approximation. In contrast with previous calculations, the
surface tension is calculated directly without recourse to integrating
thermodynamic relations. The system considered is a monovalent electrolyte with
a region at the interface, of width h, from which the ionic species are
excluded. In the case where the external dielectric constant epsilon_0 is
smaller than the electrolyte solution's dielectric constant epsilon we show
that the calculation at this order can be fully regularized. In the case where
h is taken to be zero the Onsager-Samaras limiting law for the excess surface
tension of dilute electrolyte solutions is recovered, with corrections coming
from a non-zero value of epsilon_0/epsilon.Comment: LaTeX, 14 pages, 3 figures, 1 tabl
Fermion zero-mode influence on neutron-star magnetic field evolution
The quantum phenomenon of spectral flow which has been observed in laboratory
superfluids, such as 3He-B, controls the drift velocity of proton type II
superconductor vortices in the liquid core of a neutron star and so determines
the rate at which magnetic flux can be expelled from the core to the crust. In
the earliest and most active phases of the anomalous X-ray pulsars and
soft-gamma repeaters, the rates are low and consistent with a large fraction of
the active crustal flux not linking the core. If normal neutrons are present in
an appreciable core matter-density interval, the spectral flow force limits
flux expulsion in cases of rapid spin-down, such as in the Crab pulsar or in
the propeller phase of binary systems.Comment: Additional references and extended explanation: to be published in
Monthly Notices of the Royal Astronomical Societ
Characterization of plasma thiol redox potential in a common marmoset model of agingâ
Due to its short lifespan, ease of use and age-related pathologies that mirror those observed in humans, the common marmoset (Callithrix jacchus) is poised to become a standard nonhuman primate model of aging. Blood and extracellular fluid possess two major thiol-dependent redox nodes involving cysteine (Cys), cystine (CySS), glutathione (GSH) and glutathione disulfide (GSSG). Alteration in these plasma redox nodes significantly affects cellular physiology, and oxidation of the plasma Cys/CySS redox potential (EhCySS) is associated with aging and disease risk in humans. The purpose of this study was to determine age-related changes in plasma redox metabolites and corresponding redox potentials (Eh) to further validate the marmoset as a nonhuman primate model of aging. We measured plasma thiol redox states in marmosets and used existing human data with multivariate adaptive regression splines (MARS) to model the relationships between age and redox metabolites. A classification accuracy of 70.2% and an AUC of 0.703 were achieved using the MARS model built from the marmoset redox data to classify the human samples as young or old. These results show that common marmosets provide a useful model for thiol redox biology of aging
An analysis of Australia's carbon pollution reduction scheme
The authors review the decision-making since the Labour Government came into office (November 2007). The Australian Governmentâs âCarbon Pollution Reduction Schemeâ White Paper (15 December 2008) proposes that an Australian Emissions Trading Scheme (AETS) be implemented in mid-2010. Acknowledging that the scheme is comprehensive, the paper finds that in many cases, Australia will take a softer approach to climate change through the AETS than the European Union ETS(EUETS). The paper assesses key issues in the White Paper such as emissions reduction targets, GHG coverage, sectoral coverage, inclusion of unlimited quantities of offsets from Kyoto international markets and exclusion of deforestation activities
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