30 research outputs found
Generating traffic flow and speed regional model data using internet GPS vehicle records
Nowadays, many smart-phones and vehicles are equipped with Global Position System (GPS) for tracking and navigation purposes, providing an opportunity to derive highly representative local vehicular flow and estimate vehicular emissions information. Here, we report and discuss methods used to handle large volumes of such activity data, namely 124 million GPS recordings from the web page Maplink.com.br, extract high spatial resolution vehicular flow information for a vast area in South-east Brazil, and correct for bias using traffic counts observations for the same area. The method consists in filter speed and accelerations, assign buffers to the road network, aggregate speed by street, fill missing number of lanes, generate traffic flow. Methods presented here were used to inform traffic-related air quality modelling and used as part of local air pollution management activities but are also amenable to any work that would be enhanced by more locally representative or time-resolved inputs for traffic flow, e.g. traffic network management, and demand modelling. • 124 million GPS observations from electronic devices were used to generate traffic flow. • Spatial bias was investigated and accounted for using independent local traffic count data. • Traffic count rescaled GPS traffic flow provide a robust description of spatial and quantitative traffic patterns
Potential health impact of ultrafine particles under clean and polluted urban atmospheric conditions: a model-based study
The main goal of this study was to improve the knowledge of ultrafine particle number distributions in large urban areas and also to call the attention to the importance of these particles on assessing health risks. Measurements of aerosol size distributions were performed during 2 weeks, with distinct pollutant concentrations (polluted and clean periods), on the rooftop of a building located in downtown of the megacity of São Paulo, Brazil. CO, NO2, PM10, SO2, and O3 concentrations and meteorological variables were also used. Aerosol size distribution measurements showed that geometric mean diameters of the size spectra in the polluted period are on average considerably larger than those in the clean one. Besides the fact that total number of ultrafine particles did not show significant differences, during the polluted period, geometric mean diameter was larger than during the clean one. The results of a mathematical model of particle deposition on human respiratory tract indicated a more significant effect of smaller particles fraction of the spectra, which predominate under clean atmospheric conditions. The results also indicated that urban environmental conditions usually considered good for air quality, under the criteria of low mass concentration, do not properly serve as air quality standard to very small particles. In the size range of ultrafine particles, this traditional clean atmospheric condition can offer a strong risk to pulmonary hazards, since the cleansing of the atmosphere creates good conditions to increase the concentration of nucleation mode particles
Responses of IgE, IgG1, and IgG4 to concanavalin A-binding Blomia tropicalis antigens in allergic patients
Serum and Salivary IgE, IgA, and IgG4 Antibodies to Dermatophagoides pteronyssinus and Its Major Allergens, Der p1 and Der p2, in Allergic and Nonallergic Children
Allergic rhinitis (AR) is a public health problem with high prevalence worldwide. We evaluated levels of specific IgE, IgA, and IgG4 antibodies to the Dermatophagoides pteronyssinus (Dpt) house dust mite and to its major allergens (Der p1 and Der p2) in serum and saliva samples from allergic and nonallergic children. A total of 86 children were analyzed, from which 72 had AR and 14 were nonallergic healthy children. Serum IgE and serum/salivary IgG4 levels to Dpt, Der p1, and Der p2 were higher in allergic children whereas serum/salivary IgA levels to all allergens were higher in nonallergic children. IgE levels positively correlated with IgG4 and IgA to all allergens in allergic children, while IgA levels negatively correlated with IgG4 to Dpt and Der p1 in nonallergic children. In conclusion, mite-specific IgA antibodies predominate in the serum and saliva of nonallergic children whereas mite-specific IgE and IgG4 are prevalent in allergic children. The presence of specific IgA appears to have a key role for the healthy immune response to mucosal allergens. Also, specific IgA measurements in serum and/or saliva may be useful for monitoring activation of tolerance-inducing mechanisms during allergen specific immunotherapeutic procedures, especially sublingual immunotherapy
Serum and Salivary IgE, IgA, and IgG 4 Antibodies to Dermatophagoides pteronyssinus and Its Major Allergens, Der p1 and Der p2, in Allergic and Nonallergic Children
Allergic rhinitis (AR) is a public health problem with high prevalence worldwide. We evaluated levels of specific IgE, IgA, and IgG4 antibodies to the Dermatophagoides pteronyssinus (Dpt) house dust mite and to its major allergens (Der p1 and Der p2) in serum and saliva samples from allergic and nonallergic children. A total of 86 children were analyzed, from which 72 had AR and 14 were nonallergic healthy children. Serum IgE and serum/salivary IgG4 levels to Dpt, Der p1, and Der p2 were higher in allergic children whereas serum/salivary IgA levels to all allergens were higher in nonallergic children. IgE levels positively correlated with IgG4 and IgA to all allergens in allergic children, while IgA levels negatively correlated with IgG4 to Dpt and Der p1 in nonallergic children. In conclusion, mite-specific IgA antibodies predominate in the serum and saliva of nonallergic children whereas mite-specific IgE and IgG4 are prevalent in allergic children. The presence of specific IgA appears to have a key role for the healthy immune response to mucosal allergens. Also, specific IgA measurements in serum and/or saliva may be useful for monitoring activation of tolerance-inducing mechanisms during allergen specific immunotherapeutic procedures, especially sublingual immunotherapy
Humoral and cellular immune responses to Blomia tropicalis and concanavalin A-binding fractions in atopic patients
Validação de poluentes fotoquímicos e inclusão do inventário de emissões no modelo de qualidade do ar WRF/CHEM, para a região metropolitana de São Paulo
Prediction of ground-level ozone concentration in São Paulo, Brazil: Deterministic versus statistic models
VEIN v0.2.2: an R package for bottom–up vehicular emissions inventories
Emission inventories are the quantification of pollutants from different sources. They provide important
information not only for climate and weather studies but also for urban planning and environmental health
protection. We developed an open-source model (called Vehicular Emissions Inventory – VEIN v0.2.2) that provides high-resolution vehicular
emissions inventories for different fields of studies.
We focused on vehicular sources at street and hourly levels
due to the current lack of information about these sources, mainly in developing countries.The type of emissions covered by VEIN are exhaust (hot and cold) and evaporative considering the deterioration of the factors.
VEIN also performs speciation and incorporates functions to generate and spatially allocate emissions
databases. It allows users to load their own emission factors, but it also provides emission factors
from the road transport model (Copert), the United States Environmental Protection Agency
(EPA) and
Brazilian databases. The VEIN model reads, distributes by age of use and extrapolates hourly traffic
data, and it estimates emissions hourly and spatially. Based on our knowledge, VEIN is the first bottom–up
vehicle emissions software that allows input to the WRF-Chem model. Therefore, the VEIN model provides
an important, easy and fast way of elaborating or analyzing vehicular emissions inventories under
different scenarios. The VEIN results can be used as an input
for atmospheric models, health studies, air quality standardizations and decision making
Humoral and cellular immune responses to Blomia tropicalis and concanavalin A-binding fractions in atopic patients
Blomia tropicalis, Dermatophagoides pteronyssinus and D. farinae are prevalent house dust mites. Concanavalin A-binding components derived from B. tropicalis (Bt-ConA extract) are highly immunogenic in allergic diseases. The aim of the present study was to evaluate the humoral and cellular immune responses to B. tropicalis in mite-sensitized patients. A total of 137 patients with allergic rhinitis with/without asthma and 109 non-atopic subjects were selected and analyzed by the skin prick test, and for total serum IgE and specific IgE levels to both Bt-total and Bt-ConA extracts, their proliferative response and cytokine (IFN-γ and IL-5) production by peripheral blood mononuclear cells (PBMC) stimulated with both extracts. Skin prick test showed that 70% of the patients were sensitized to Bt (Bt+) and similar levels of specific IgE to Bt-total and Bt-ConA extracts were demonstrable in Bt+ patients. Significant PBMC proliferation was observed in response to Bt-total extract in Bt+, but not in Bt- patients and non-atopic subjects (P < 0.001). Bt-ConA extract induced increased proliferative responses in all patient groups compared to medium alone (P < 0.05), but these responses were significantly decreased in the presence of the mannopyranoside ConA inhibitor (P < 0.05). Significant IFN-γ production was observed after Bt-ConA stimulation of Bt+ patients (P < 0.05), while Bt-total extract had no effect. IL-5 production was consistently detected in Bt+ patients after allergen-specific stimulation or with no stimulus, indicating that PBMC from allergic patients are prone to produce Th2 profile cytokines, spontaneously or inductively by allergen restimulation. These data showed that ConA-binding components isolated from B. tropicalis may contain relevant antigens that are involved in both humoral and cellular immune responses. However, without an additional purification procedure to eliminate the residual contamination with ConA, its use in immunotherapeutic procedures cannot be recommended