Study on the relationship between the incidence of influenza and climate indicators and the prediction of influenza incidence

In recent 2 years, the incidence of influenza showed a slight upward trend in Guangxi; therefore, some joint actions should be done to help preventing and controlling this disease. The factors analysis of affecting influenza and early prediction of influenza incidence may help policy-making so as to take effective measures to prevent and control influenza. In this study, we used the cross correlation function (CCF) to analyze the effect of climate indicators on influenza incidence, ARIMA and ARIMAX (autoregressive integrated moving average model with exogenous input variables) model methods to do predictive analysis of influenza incidence. The results of CCF analysis showed that climate indicators (PM2.5, PM10, SO₂, CO, NO2, O₃, average temperature, maximum temperature, minimum temperature, average relative humidity, and sunshine duration) had significant effects on the incidence of influenza. People need to take good precautions in the days of severe air pollution and keep warm in cold weather to prevent influenza. We found that the ARIMAX (1,0,1)(0,0,1)₁₂ with NO₂ model has good predictive performance, which can be used to predict the influenza incidence in Guangxi, and the predicted incidence may be useful in developing early warning systems and providing important evidence for influenza control policy-making and public health intervention.

     

Briquettes of acai seeds: characterization of the biomass and influence of the parameters of production temperature and pressure in the physical-mechanical and energy quality

Environmental Science and Pollution Research - Agro-industries, leveraged by the high demand of acai products, promote environmental impact through the generation of wastes in several locals in...     

An assessment of the environmental fate and exposure of benzene and the chlorobenzenes in Canada

Systematic modelling of the fate of benzene and the chlorobenzenes is presented which follows a four-stage process of chemical classification, quantifying discharge rates and environmental concentrations, evaluative assessment of fate and regional mass balance modelling has been carried out for the southern Ontario region. The EQC model was applied to determine the principal transport and transformation processes experienced by this group of chemicals, which vary considerably in volatility and hydrophobicity. Observed environmental concentrations are in satisfactory agreement with the predictions of the steady state Level III ChemCAN model of chemical fate. A multiple pathway human exposure model which estimates intake of contaminants by residents of southern Ontario has been developed and applied to these chemicals. A novel method of deducing maximum tolerable environmental concentrations is presented. Results suggest that benzene and 1,4-dichlorobenzene are present in the environment at levels sufficient to cause exposures near allowable daily intake (ADI) levels for the general population, but the other substances are present at levels which result in exposure ranging from 1/10 to 1/1000 of the ADI.     

Characterization and application of the enzyme peroxidase to the degradation of the mycotoxin DON

Deoxynivalenol (DON), one of the main mycotoxins found in food matrices, has high level of toxicity. This study aimed to characterize the peroxidase enzyme extracted from rice bran to be applied to the biodegradation of DON in order to evaluate the potential peroxidase (PO) from rice bran (RB) has to degrade DON in optimal conditions. Purification and recovery factors of PO extracted from RB and purified by three-phase partitioning were 5.7% and 50%, respectively. PO had the highest level of activity in the phosphate buffer 5 mM pH 5.5 in both crude and purified forms, whose reaction temperatures were 25°C and 10°C. At the end of production, purification and characterization steps, specific activities of the bran were 115.79 U mg^?1 and 4363 U g^?1. Reduction in the mycotoxin DON in optimal conditions determined for PO from RB was 20.3%, a promising result when the aim is to adequate mycotoxicological levels to foods.     

Sedimentation of PCDD/Fs and PCBs in the Gulf of Finland and the Gulf of Bothnia,the Baltic Sea

Sediment trap material was collected during May–December in the period 1996–2008 in three coastal areas and four open sea stations in the Finnish territory of the Baltic Sea. The highest sedimentation of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) with a typical source-related congener profile from chlorophenol production dominated by highly chlorinated dibenzofurans was found close to a historical source in the Kymijoki estuary. This was an order of magnitude higher than in other river estuaries and two orders of magnitude higher than in the open sea stations. The sedimentation of polychlorinated biphenyls (PCBs) was also higher in river estuaries than in other areas. No significant decrease over a 12 year period of monitoring was found in concentration or in sedimentation in the Kymijoki estuary. In the western Gulf of Finland, the Archipelago Sea and the Gulf of Bothnia, the dominating congeners, calculated as toxic equivalent (TEQ) in sedimentation were 1, 2, 3, 7, 8-PeCDD and 2, 3, 4, 7, 8-PeCDF, often reported as the main congeners in deposition.     

Absorption and metabolism of the chiral isomers of fonofos in the corn and cotton plant

Root absorption of chiral phenyl-35S-fonofos in cotton and corn plants revealed stereoselective differences between the two enantiomers. (S)p-Fonofos was absorbed at a faster initial rate and to a greater extent than the (R)p enantiomer in both plant species. Approximately 40% and 62% of the applied radioactivity was absorbed into the cotton plant 12 hr after application of (R)p- and (S)p-fonofos, respectively. In the corn plant, approximately 25% and 63% of the applied (R)p- and (S)p-fonofos was absorbed in the first 12 hrs. Little qualitative or quantitative difference in plant translocation between fonofos enantiomers was observed. (R)p-fonofos was found to be metabolized to a greater extent than the (S)p enantiomer in both cotton and corn plants.     

森林降水化学的变化特征和机理

研究并比较了湖南酸雨区韶山小集水区林内降水的化学特征，结果表明，与大气降水相比，穿冠水和地表穿透水中的富集的离子浓度除了NO3^-和Na^ 外均明显增加，到达地表的降水离子增加倍数最高达34．3倍；离子总量最高倍数为8．1倍，乔木树冠层的离子富集作用大于灌木层。韶山的大气降水、穿冠水和地表穿透水的年均pH分别为4．61、5．54和5．85。持续大量的降水对森林上空的污染物有较高的清除效果。     

Relationship between the ATP content of subsurface material and the rate of biodegradation of alkylbenzenes and chlorobenzene

The rate of biotransformation of toluene in unconsolidated subsurface material from sites at Lula, Oklahoma, and Conroe, Texas, was compared to the ATP (adenosine triphosphate) content of these materials. The rate of toluene degradation decreased with decreasing ATP content. When ATP contents were at or less than 0.05 ng g⁻¹, biotransformation of toluene could not be detected (less than 1% of the initial concentration was degraded per week). At intermediate concentrations of ATP, 0.37 and 0.16 ngvg⁻¹, the rates of toluene degradation were 18 ± 4.5% and 25 ± 10% of the initial concentration per week. At ATP concentrations above 1 ng g⁻¹, the rates of toluene degradation exceeded 90% of the initial concentration per week. There was no simple relationship between ATP content and chlorobenzene degradation. Subsurface material that had been exposed to creosote wastes, and which degraded toluene rapidly, also degraded benzene, o-xylene, and m-xylene.     

Chlorophyll, carotenoids and the activity of the xanthophyll cycle

Clone spruce trees (Picea abies L. Karst.) were exposed in the Hohenheim open-top chambers to low levels of O(3) and SO(2), singly and in combination, and to simulated precipitation of two pH treatments (Seufert et al., this volume). At the end of five years of continuous exposure, needles from the 13-year-old trees were sampled and analysed for pigments content by means of HPLC (high pressure liquid chromatography). The pigment content was determined for three needle age classes. Chlorophyll a content, measured on a dry weight basis, was similar for all needle age classes in the control chambers receiving only the simulated rain treatments at pH 5.0 or 4.0, and the chamber receiving O(3) and the rain treatment at pH 4.0. Also, no differences were noted in one-year-old needles in the chambers with SO(2) and simulated precipitation at pH 4.0 and SO(2) + O(3) and simulated precipitation at pH 4.0. Reductions of approximately 10 and 35% were measured in two-year-old needles from the chambers with SO(2) and precipitation at pH 4.0, and SO(2) + O(3) and precipitation at pH 4.0. The three-year-old needles from these chambers had 40% lower chlorophyll a content compared to the control chambers. No treatment effects were seen on the molar ratios of chlorophyll b, the carotenes, lutein, neoxanthin, and the sum of carotenoids involved in the xanthophyll cycle, violaxanthin + antheraxanthin + zeaxanthin, to chlorophyll [Formula: see text]. The xanthophyll cycle, assayed in one-year-old needles under defined light conditions (520 microE m(-2) s(-1), while light) was active in all samples. Needles from the control chambers and the chambers with SO(2) and with O(3) behaved similarly and differed from the SO(2) + O(3) treated needles by a 50% higher zeaxanthin content reached under light.     

Photodegradation of the herbicide EPTC and the safener dichlormid, alone and in combination

Photodegradation of the herbicide EPTC (S-ethyl-N, N-dipropylthiocarbamate), and the safener dichlormid (2,2-dichloro-N, N-diallylacetamide) has been examined in methanol and in water solutions. Irradiation of EPTC and dichlormid with UV light at 254 nm caused rapid degradation in both media. Remarkable and gradual changes in color of EPTC irradiated solution was observed from clear to yellow then to intense orange. EPTC half-life of elimination in water was 14.0, and 18.5 min, and in methanol 37.2 and 32.2 min, when irradiated with and without dichlormid, respectively. There was significant difference between rate of EPTC degradation in water and methanol in the presence or in the absence of dichlormid. Negligible degradation of EPTC or dichlormid at > 290 nm was observed. Photoproducts were separated and identified using GC or/and thin-layer chromatography then identified using mass spectrometry. It appeared that some products have high molecular weight that formed as a result of dimerization. This is possibly a result of the coupling of radicals that formed through EPTC degradation. The cleavage of C-S and C-N bonds accounted for the formation of these radicals. Gradual dealkylation of the acid chains of EPTC has also occurred. EPTC-sulfoxide, EPTC-sulfone, Propylamine and dipropylamine were detected as photoproducts of EPTC at 254 nm. Dichlormid pathways of degradation at 254 nm were characterized as dechlorination, dealkylation, and hydrolysis both in water and methanol. The findings showed that dichlormid did not significantly affect EPTC photodegradation either at 254 nm or at > 290 nm. The biological/toxicological properties of the photoproducts need further study, particularly the dimer compounds.     

Mining, the environment and the treatment of mine effluents

The environmental impact of mining on the ecosystem, including land, water and air, has become an unavoidable reality. Guidelines and regulations have been promulgated to protect the environment throughout mining activities from start-up to site decommissioning, in particular, the occurrence of acid mine drainage (AMD), due to oxidation of sulfide mineral wastes, has become the major area of concern to many mining industries during operations and after site decommissioning. AMD is characterised by high acidity and a high concentration of sulfates and dissolved metals. If it cannot be prevented or controlled, it must be treated to eliminate acidity, and reduce heavy metals and suspended solids before release to the environment. This paper discusses conventional and new methods used for the treatment of mine effluents, in particular the treatment of AMD.     

Industrial plastic on the southern beaches of the Arabian Gulf and the western beaches of the Gulf of Oman

The increasing production and use of plastic in the Arabian Gulf combined with shipping and waste disposal practices, have increased the concentration of plastic particles on the sea's surface and beaches. The objective of this investigation was to provide an assessment of the abundance, distribution, potential sources and significance of industrial plastic on the western beaches of the United Arab Emirates on the Arabian Gulf and on the eastern beaches on the Gulf of Oman. The abundance of stranded plastic pellets was highly uneven. By early 1992 alarming levels of fresh plastic pellets were noticed on the Arabian Gulf beaches of the UAE. Large numbers of 25 kg sacks of white plastic spherules manufactured by (SABIC) in Jubail, Saudi Arabia were washed ashore. When compared to the west coast on the Arabian Gulf, the east coast on the Gulf of Oman exhibited much lower levels of plastic pellets. When compared to other parts of the world, the beaches of the UAE on the Arabian Gulf are considered to be heavily polluted with industrial plastic.     

Modelling the atmospheric transport and deposition of sulphur and nitrogen over the United Kingdom and assessment of the influence of SO2 emissions from international shipping

A statistical Lagrangian atmospheric transport model was used to generate annual maps of deposition of sulphur and oxidised and reduced nitrogen for the UK at a 5×5 km² resolution. The model was run using emissions for the year 2002. The model was compared with measurements of gas concentrations (SO₂, NO_x, HNO₃ and NH₃) and of wet deposition and aerosol concentrations of SO₄²⁻, NO₃⁻ and NH₄⁺ from national monitoring networks. Good correlation was obtained, demonstrating that the model is capable of accurately estimating the mass balance and spatial distribution of sulphur and nitrogen compounds in the atmosphere. A future emissions scenario for the year 2020 was used to test the influence of shipping emissions on sulphur deposition in the UK. The results show that, if shipping emissions are assumed to increase at a rate of 2.5% per year, their relative contribution to sulphur deposition is expected to increase from 9% to 28% between 2002 and 2020. The model was compared to both a European scale and a global scale chemical transport model and found to give broad agreement with the magnitude and location of sulphur deposition associated with shipping emissions. Enforcement of the MARPOL convention to reduce the sulphur content in marine fuel to 1% was estimated to result in a 6% reduction in total sulphur deposition to the UK for the year 2020. The percentage area of sensitive habitats with exceedance of critical loads for acidity in the UK was predicted to decrease by 1% with the implementation of the MARPOL convention.     

Attempts to probe the ozone layer and the ultraviolet-B levels of the past

To get a proper perspective on the current status of atmospheric ozone, which protects the biosphere from ultraviolet-B (UV-B; 280-315 nm) radiation, it would be of value to know how ozone and UV-B radiation have varied in the past. The record of worldwide ozone monitoring goes back only a few decades, and the record of reliable UV-B measurements is even shorter. Here we review indirect methods to assess their status further back in time. These include variations in the Sun's emission and how these affect the atmosphere, changes in the Earth's orbit, geologic imprints of atmospheric ozone, effects of catastrophic events such as volcanic eruptions, biological proxies of UV-B radiation, the spectral signature of terrestrial ozone in old recordings of star spectra, and the modeling of UV-B irradiance from ozone data and meteorological recordings. Although reliable reconstructions do not yet extend far into the past, there is some hope for future progress.     

Optimization and characterization of the formation of oil-in-water diazinon nanoemulsions: Modeling and influence of the oil phase,surfactant and sonication

Nanoemulsions are particularly suitable as a platform in the development of delivery systems for lipophilic functional agents. Current research describes the formation of oil-in-water (O/W) diazinon nanoemulsions using synthetic and natural additives by adopting a high-energy (ultrasound) emulsification method. The diazinon nanoemulsions were spontaneously formed by adding dropwise a mixture of diazinon, solvent and co-solvent in an aqueous solution containing a surfactant (tween or lecithin) with continuous stirring. The nanoemulsions were then formed by ultra-sonication. The effects of three levels of active ingredient, solvent, co-solvent, surfactant, sonication time and sonication cycle and power were performed by Minitab software to design the experiment. Effects of these factors on droplet size, polydispersity index (PDI), viscosity and pH of nanoemulsions were investigated. The results of the modeling showed that the experimental data could be adequately adapted in a second-order polynomial model with a multiple regression coefficient r² of 0.821 for the prediction of particle size, PDI and viscosity. The long-term and thermodynamic stability of the prepared nanoemulsions were tested. The droplet size and morphology of the nanoemulsions were measured by dynamic light scattering (DLS) and transmission electron microscopy (TEM). On this basis, a water-insoluble insecticide diazinon was incorporated into 26 optimized nanoemulsion systems to demonstrate potential applications in pest control. The results of DLS and TEM measurements showed that most of prepared nanoemulsions had an almost monodisperse droplet size distribution (PDI < 200 nm). Incorporation of diazinon had no significant effect on the size and stability of the nanoemulsions and the formulated nanoemulsion remained stable after four months of storage.     

Comparing the Community Composition of European and Eastern Chinese Waterbirds and the Influence of Human Factors on the China Waterbird Community

We compared the European and eastern Chinese waterbird assemblages and checked whether the effects of human disturbance could be detected in the assemblages’ composition. For the different Chinese provinces, we expected to find a negative effect of economic development on the mean bird species mass and on the proportion of bentivorous, piscivorous and insectivorous bird species. We also expected to find relatively fewer large species in the Chinese assemblage. Species rank–abundance curves were relatively similar, but China had significantly more species with smaller body masses. The China assemblage was characterized by relatively higher abundance of heavy-bodied species, contrary to our expectations. Mean bird body mass decreased in China with increasing disturbance and increasing gross domestic product (GDP). For coastal provinces in China the percentage of bentivorous, piscivorous and insectivorous bird species declined with increasing GDP, maybe through the increased use of pesticides or fertilizer.     

Biodegradability of the anticancer drug etoposide and identification of the transformation products

Etoposide susceptibility to microbiological breakdown was studied in a batch biotransformation system, in the presence or absence of artificial wastewater containing nutrients, salts and activated sludge at two concentration levels. The primary focus of the present study was to study etoposide transformation products by ultra-high performance liquid chromatography coupled to high-resolution hybrid quadrupole-Orbitrap tandem mass spectrometry (MS/MS). Data-dependent experiments combining full-scan MS data with product ion spectra were acquired to identify the molecular ions of etoposide transformation products, to propose the molecular formulae and to elucidate their chemical structures. Due to the complexity of the matrix, visual inspection of the chromatograms showed no clear differences between the controls and the treated samples. Therefore, the software package MZmine was used to facilitate the identification of the transformation products and speed up the data analysis. In total, we propose five transformation products; among them, four are described as etoposide transformation products for the first time. Even though the chemical structures of these new compounds cannot be confirmed due to the lack of standards, their molecular formulae can be used to target them in monitoring studies.     

Outdoor air pollution exposure and the risk of asthma and wheezing in the offspring

Environmental Science and Pollution Research - According to the “fetal origin of disease” hypothesis, air pollution exposure in pregnancy may play an important role in stimulating the...     

Qualitative evaluation of the mineralogical and chemical composition of dry deposition in the central and southern highlands of Jordan

The chemical and mineralogical composition of dry deposition in the western highlands of central and south Jordan at the end of the summer season 2000, reflect the composition of soils in addition to anthropogenic activities at these areas. Calcite predominated in the central region whereas calcite and quartz are the dominant minerals in south Jordan. The concentrations of Hg, Cr, Ni, Cu, Pb and Zn were higher in central Jordan, which might be attributed to higher anthropogenic activities than south. On the other hand, Fe, Mn, Ti, Ba, Sr, Y and Rb were higher in the south of Jordan reflecting the composition of soil at these sites. At Aqaba city, the only port of Jordan, where Cr, Cd, As and S were higher than other areas. This variation might be attributed to the contribution of phosphate dust in the atmosphere through handling processes.     

Measurements and analyses of nitrogen oxides and ozone in the yard and on the roof of a street-canyon in Suzhou

The concentrations of air pollutants such as nitrogen oxides and ozone characterised by very fast chemical reactions can significantly vary within urban street-canyon due to the short distances between sources and receptor. With the primary objective to analyse this issue, NO, NO₂, NO_x, O₃, BTX, and wind flow field were continuously measured for 1 week at two heights (a street-level yard and a 25-m-high rooftop) in an urban canyon in Suzhou (China). The yard ozone concentrations were found to be up to six times lower than on the roof. Different frequency distributions (FD), dynamical and chemical processes of the pollutant variations from yard to roof are discussed to explain the findings. The predominant factors for the dissimilar pollutant vertical diffusion at the two measurement locations were associated to dissimilar fluid-dynamic and heterogeneous removal effects that likely induced dissimilar ozone chemical processes relative to NO_x and BTX precursors.