Assessment and sources of nonaromatic hydrocarbons in surface sediments of three harbors in Santa Catarina State, Brazil

Nonaromatic hydrocarbons and geochemical parameters from 17 sediment?Cwater interface samples were used to assess sources of organic matter in three harbors, located in Santa Catarina State, southern Brazil. The evaluation was based on the molar C/N/P ratios, abundance of resolved nonaromatic hydrocarbons (3.0?C25.9 ??g g^???1), unresolved complex mixture, and two indexes: the carbon preference index (CPI) and the low molecular weight to high molecular weight ratio. The results indicate that the organic matter is predominantly of terrestrial origin (C/N > 10 and CPI > 2). Variations in the total organic carbon from 0.43 to 2.98 mmol g^???1 and total phosphorus from 82.4 to 464.3 ??g g^???1 showed no clear correlation with the silt and clay fractions of the sediments possibly due to anthropogenic input. In contrast to the low level of contamination based on the acyclic hydrocarbon distribution, the results obtained from a series of geologically stable hopanes and steranes reveal the presence of less degradable petroleum derivatives.     

Coal cleaning residues and Fe-minerals implications

In the present investigation, a study was undertaken to understand the origin of Fe-minerals presents in Brazilian coal mining and to understand the environmental implication and the chemical heterogeneity in the study area. Coal cleaning residue samples rich in clays, quartz, sulphides, carbonates, sulphates, etc. were sampled from Lauro Muller, Urussanga, Treviso, Siderópolis, and Criciúma cities in the Santa Catarina State and a total of 19 samples were collected and Mössbauer, XRD, SEM/EDX, and TEM analyses were conducted on the samples. The major Fe-minerals identified are represented by the major minerals chlorite, hematite, illite, and pyrite, while the minor minerals include, ankerite, chalcopyrite, goethite, hematite, jarosite, maghemite, magnetie, marcasite, melanterite, natrojarosite, oligonite, pyrrhotite, rozenite, schwertmannite, siderite, and sideronatrile. Pyrite is relatively abundant in some cases, making up to around 10% of the mineral matter in several samples. The sulphates minerals such as jarosite and others, probably represent oxidation products of pyrite, developed during exposure or storage.     

Thermotolerant coliform loadings to coastal areas of Santa Catarina (Brazil) evidence the effect of growing urbanisation and insufficient provision of sewerage infrastructure

Thermotolerant coliform (TC) loadings were quantified for 49 catchments draining into the North and South Bays of Santa Catarina (SC, southeastern Brazil), an area known for its tourism and aquaculture. TC loadings were calculated based on flow measurements taken in 26 rivers. TC concentrations ere quantified based on surface water samples collected at 49 catchment outlets in 2012 and 2013. Median TC loads ranged from 3.7 × 10³ to 6.8 × 10⁸ MPN s^?1. TC loadings in the catchments increased in proportion to increases in resident human population, population density and percentage of urbanised area. Catchments with more than 60% of area covered by wastewater collection and treatment systems had higher TC loads per person than catchments with less than 25%. Based on the study catchments, these results indicate that current sewerage infrastructure is ineffective in reducing contamination of faecal origin to surface waters. These findings have important implications for the management of microbiological health hazards in bathing, recreational and shellfish aquaculture waters in the North and South Bays of Santa Catarina Island.     

Prevalence of heavy metal resistance in bacteria isolated from tannery effluents and affected soil

In the present study, a total of 198 bacteria were isolated, 88 from the tannery effluents and 110 from agricultural soil irrigated with the tannery effluents. Tannery effluents and soils were analyzed for metal concentrations by atomic absorption spectrophotometer. The tannery effluents and soil samples were found to be contaminated with chromium, nickel, zinc, copper, and cadmium. All isolates were tested for their resistance against Cr^6?+?, Cr^3?+?, Ni^2?+?, Zn^2?+?, Cu^2?+?, Cd^2?+?, and Hg^2?+?. From the total of 198 isolates, maximum bacterial isolates were found to be resistant to Cr^6?+? 178 (89.9%) followed by Cr^3?+? 146 (73.7%), Cd^2?+? 86 (43.4%), Zn^2?+? 83 (41.9%), Ni^2?+? 61 (30.8%), and Cu^2?+? 51 (25.6%). However, most of the isolates were sensitive to Hg^2?+?. Among the isolates from tannery effluents, 97.8% were resistant to Cr^6?+? and 64.8% were resistant to Cr^3?+?. Most of the soil isolates were resistant against Cr^6?+? (83.6%) and Cr^3?+? (81.8%). All isolates were categorized into Gram-positive and Gram-negative bacteria. In a total of 114 Gram-positive isolates, 91.2% were resistant to Cr^6?+? followed by 73.7% to Cr^3?+?, 42.1% to Zn^2?+?, 40.4% to Cd^2?+?, and 32.5% to Ni^2?+?. Among Gram-negative isolates, 88.1% were found showing resistance to Cr^6?+?, 75.0% to Cr^3?+?, and 47.6% were resistant to Cd^2?+?. Majority of these metal-resistant isolates were surprisingly found sensitive to the ten commonly used antibiotics. Out of 198 isolates, 114 were found sensitive to all antibiotics whereas only two isolates were resistant to maximum eight antibiotics at a time. Forty-one and 40 isolates which constitute 20.7% and 20.2% were resistant to methicilin and amoxicillin, respectively.     

Bacteria with dual resistance to elevated concentrations of heavy metals and antibiotics in Nigerian contaminated systems

Samples of soil, water, and sediments from industrial estates in Lagos were collected and analyzed for heavy metals and physicochemical composition. Bacteria that are resistant to elevated concentrations of metals (Cd^2?+?, Co^2?+?, Ni^2?+?, Cr^6?+?, and Hg^2?+?) were isolated from the samples, and they were further screened for antibiotic sensitivity. The minimum tolerance concentrations (MTCs) of the isolates with dual resistance to the metals were determined. The physicochemistry of all the samples indicated were heavily polluted. Twenty-two of the 270 bacterial strains isolated showed dual resistances to antibiotics and heavy metals. The MTCs of isolates to the metals were 14 mM for Cd^2?+?, 15 mM for Co^2?+? and Ni^2?+?, 17 mM for Cr^6?+?, and 10 mM for Hg^2?+?. Five strains (Pseudomonas aeruginosa, Actinomyces turicensis, Acinetobacter junni, Nocardia sp., and Micrococcus sp.) resisted all the 18 antibiotics tested. Whereas Rhodococcus sp. and Micrococcus sp. resisted 15 mM Ni^2?+?, P. aeruginosa resisted 10 mM Co^2?+?. To our knowledge, there has not been any report of bacterial strains resisting such high doses of metals coupled with wide range of antibiotics. Therefore, dual expressions of antibiotics and heavy-metal resistance make the isolates, potential seeds for decommissioning of sites polluted with industrial effluents rich in heavy metals, since the bacteria will be able to withstand in situ antibiosis that may prevail in such ecosystems.     

Effects of cement flue dusts from a Nigerian cement plant on air, water and planktonic quality

Effects of cement flue dust from Ewekoro cement Kilns were monitored at some aquatic receptor locations. High levels of total suspended particulates (TSPs) and atmospheric deposition rates (ADRs) were recorded within the factory compared to ancillary locations outside the factory. The TSP and ADR levels which were location dependent were significantly higher (P?<?0.05) during the dry periods than in the wet season. Irrespective of seasonal variations, the key elements in the emissions were Ca^2?+? and Fe^2?+?. The concentrations of Zn^2?+?, Mn^2?+? and Pb^?+? which were trace elements were significantly higher (P?<?0.05) in the deposited than in the airborne particulates. The planktonic flora and fauna of the river systems draining the area were poor with 16 phytoplanktonic and nine zooplanktonic species. Numerically, the phytoplanktons were dominated by diatoms (Bacillariophyta) with Synedra sp. being the most abundant species. The zooplanktonic fauna dominated by rotifers had Lecane curvicornis as a regular occurrence in all the three catchment rivers. The physicochemical parameters assayed were significantly higher (P?<?0.05) in the factory effluent discharges than in water samples from each of the catchment rivers. Seasonal variations inclusive, HCO $_{3}^{-}$ , CO $_{3}^{2-}$ , Ca^2?+? and Mg^2?+? constituted the major ionic component of water samples analysed irrespective of location. Alaguntan River which receives effluents directly from the factory had significantly higher levels (P?<?0.05) of the assayed ions than the other two rivers draining the cement factory catchment areas.     

Identification of the hydrogeochemical processes in groundwater using major ion chemistry: a case study of Penna–Chitravathi river basins in Southern India

Hydrogeochemical studies were carried out in the Penna–Chitravathi river basins to identify and delineate the important geochemical processes which were responsible for the evolution of chemical composition of groundwater. The area is underlain by peninsular gneissic complex of Archaean age, Proterozoic meta-sediments, and strip of river alluvium. Groundwater samples were collected covering all the major hydrogeological environs in pre- and post-monsoon seasons. The samples were analyzed for major constituents such as Ca^2?+?, Mg^2?+?, Na^?+?, K^?+?, CO₃ ^???, HCO₃ ^???, Cl^???, SO₂ ^???4, NO₃ ^???, and F^???. The groundwater in general is of Na^?+?–Cl^???, Na^?+?–HCO₃ ^???, Ca^2?+?–Mg^2?+?–HCO₃ ^???, and Ca^2?+?–Mg^2?+?–Cl^??? types. Na^?+? among cations and Cl^??? and/or HCO₃ ^??? among anions dominate the water; Na^?+? and Ca^2?+? are in the transitional state with Na^?+? replacing Ca^2?+? and HCO₃ ^??? Cl^??? due to physiochemical changes in the aquifer and water–rock interactions. The Ca^2?+?–Mg^2?+?–Cl^??? HCO₃ ^??? type water in one third samples suggest that ion exchange and dissolution processes are responsible for its origin. Change in storage of aquifer in a season does not influence the major geochemical makeup of groundwater. Gibbs plots indicate that the evolution of water chemistry is influenced by water–rock interaction followed by evapotranspiration process. The aquifer material mineralogy together with semiarid climate, poor drainage system, and low precipitation factors played major role in controlling groundwater quality of the area.     

Incidence of metal and antibiotic resistance in Pseudomonas spp. from the river water, agricultural soil irrigated with wastewater and groundwater

A total of 144 isolates of Pseudomonas spp. (48 each from the Yamuna River water, wastewater irrigated soil and groundwater irrigated soil) were tested for their resistance against certain heavy metals and antibiotics. Minimum inhibitory concentrations (MICs) of Hg^2?+?, Cd^2?+?, Cu^2?+?, Zn^2?+?, Ni^2?+?, Pb^2?+?, Cr^3?+? and Cr^6?+? for each isolate were also determined. A maximum MIC of 200 ??g/ml for mercury and 3,200 ??g/ml for other metals were observed. The incidences of metal resistance and MICs of metals for Pseudomonas isolates from the Yamuna water and wastewater irrigated soil were significantly different to those of groundwater irrigated soil. A high level of resistance against tetracycline and polymyxin B (81.2%) was observed in river water isolates. However, 87.5% of Pseudomonas isolates from soil irrigated with wastewater showed resistance to sulphadiazine, whereas 79.1% were resistant to both ampicillin and erythromycin. Isolates from soil irrigated with groundwater exhibited less resistance towards heavy metals and antibiotics as compared to those of river water and wastewater irrigated soil. Majority of the Pseudomonas isolates from water and soil exhibited resistance to multiple metals and antibiotics. Resistance was transferable to recipient Escherichia coli AB2200 strains by conjugation. Plasmids were cured with the curing agent ethidium bromide and acridine orange at sub-MIC concentration.     

Monitoring the formation of trihalomethanes in the effluents from a shrimp hatchery

Formation of trihalomethanes (THM) was monitored at the Laboratório de Camarões Marinhos (LCM) from the Universidade Federal de Santa Catarina. THM could be present because chlorinated effluents from disinfection are discharged from the different hatchery rooms. THM quantification was done through an analytical methodology using Purge&;Trap coupled with a gas chromatograph equipped with an electron capture detector. Relative standard deviation (RSD), limit of detection (LOD) and limit of quantification (LOQ) for the methodology corresponded to the ranges of 8–17%; 0.01–0.03 μg L^?1 and 0.03–0.08 μg L^?1, respectively. Linear working range was of 0.1–8.0 μg L^?1 for all compounds. Enrichment and recovery method was applied to evaluate possible matrix effects and the results varied from 71.2% to 107.9%. LCM was monitored between August and December, 2004. This study showed that THM did not increase with the increase in postlarvae production and also that the aquatic life and the surrounding environment were not affected.     

2020年泰州市细颗粒物质量浓度高值区污染来源解析

2020年在位于泰州市主城区大气细颗粒物(PM_(2.5))质量浓度高值区的莲花国控空气站点进行手工采样,分析了大气PM_(2.5)的质量浓度和元素组成,以及离子、有机碳和元素碳的质量浓度。根据监测结果,采用正定矩阵因子分解(PMF)受体模型对其来源进行解析。结果显示,莲花站点大气PM_(2.5)中主要组分包括有机物、硝酸盐、硫酸盐、铵盐、地壳物质、氯盐、钾盐、黑炭、微量元素和钠盐,占比分别为35.7%,25.6%,13.9%,11.9%,6.1%,2.3%,1.5%,1.5%,0.8%和0.7%,有机物、硝酸盐、硫酸盐、铵盐为首要污染组分,这4类物质对PM_(2.5)的累计贡献为87.1%。根据解析结果与实际污染特征,提出应优化城市路网结构,强化工地扬尘管控,全面取缔燃煤炉和严抓秸秆禁烧工作等控制对策。     

工业链条炉燃用型煤与原煤颗粒物排放特征

选取燃烧型煤和原煤的典型链条炉,应用自行设计的固定源烟气颗粒物稀释采样系统,现场测试细颗粒物PM_(2.5)、PM_(10)和金属元素的排放特征。结果表明,型煤燃烧细颗粒物的排放比例高于原煤,型煤燃烧除尘器进口、出口PM_(2.5)质量比原煤燃烧分别增加715%和708%。燃烧型煤时,As和Pb在各粒径段的质量比均比原煤大。同时,由于型煤燃烧可吸入颗粒物的排放比例增加,包含或附着在烟尘上的金属元素排放比例也相应增加。     

Urban and suburban aerosol in Yokohama, Japan: a comprehensive chemical characterization

This article analyses elemental composition of suspended particulate matter (SPM) samples collected monthly from 1999 to 2005 at two locations in Yokohama, Japan. Microwave digestion and inductively coupled plasma mass spectroscopy was employed to measure Mg, Al, Ca, V, Cr, Mn, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Pb, and Bi. Water-soluble ions (Na^?+?, NH₄ ^?+?, K^?+?, Ca^2?+?, Cl^???, NO₃ ^???, and SO₄ ^2???) and carbonaceous mass (elemental and organic carbon) were detected using ion chromatograph and CHN analyzer, respectively. The results indicate that the composition of SPM on one of the sites is determined by automobile emissions and on the other by industrial combustions. The impact of the emission regulations for automobiles in large Japanese cities, which were enacted during 2002 and 2003, on the SPM composition of the samples is also studied.     

Observational and modeling study of dry deposition on surrogate surfaces in a South China city: implication of removal of atmospheric crustal particles

Dry deposition samples collected during 1999–2001 at a South China site using surrogate surfaces were analyzed by capillary electrophoresis. Collector surface properties played important roles to the dry deposition. The deposition velocities for various species ranged from 0.02 to 1.69 cm s^???1, in general agreement with literature values. More than 90% of Ca^2?+? was deposited by sedimentation and its comparable values of dry or wet removal residence times imply that dry deposition is an important atmospheric removal process for the ubiquitous crustal species in South China, compared with precipitation scavenging. Relatively good agreement was found when the species deposition velocities were modeled based on up-to-date knowledge of particle dry deposition. The total depositions for anthropogenic and crustal species in northern China are likely to be much higher than those in the south, including our site where the fluxes of the acidic species SO₄ ^2??? and NO₃ ^??? were 4.4 and 2.2 g m^???2 year^???1, respectively. The sum of dry deposition for cations Na^?+?, Ca^2?+?, Mg^2?+?, and K^?+? contributes 44% of the total flux, which is equivalent to the value estimated in Europe.     

Characteristics of Hazardous Airborne Dust Around an Indian Surface Coal Mining Area

Surface coal mining creates more air pollution problems with respect to dust than underground mining . An investigation was conducted to evaluate the characteristics of the airborne dust created by surface coal mining in the Jharia Coalfield. Work zone air quality monitoring was conducted at six locations, and ambient air quality monitoring was conducted at five locations, for a period of 1 year. Total suspended particulate matter (TSP) concentration was found to be as high as 3,723 μg/m³, respirable particulate matter (PM10) 780 μg/m³, and benzene soluble matter was up to 32% in TSP in work zone air. In ambient air, the average maximum level of TSP was 837 μg/m³, PM10 170 μg/m³ and benzene soluble matter was up to 30%. Particle size analysis of TSP revealed that they were more respirable in nature and the median diameter was around 20 μm. Work zone air was found to have higher levels of TSP, PM10 and benzene soluble materials than ambient air. Variations in weight percentages for different size particles are discussed on the basis of mining activities. Anionic concentration in TSP was also determined. This paper concludes that more stringent air quality standards should be adopted for coal mining areas and due consideration should be given on particle size distribution of the air-borne dust while designing control equipment.     

Seasonal variation, source, and regional representativeness of the background aerosol from two remote sites in western China

Using observations from two remote sites during July 2004 to March 2005, we show that at Akdala (AKD, 47° 06′ N, 87° 58′ E, 562 m asl) in northern Xinjiang Province, there were high wintertime loadings of organic carbon (OC), elemental carbon (EC), and water-soluble (WS) ${\rm SO}_{4}^{2-}$ , ${\rm NO}_{3}^{2-}$ , and ${\rm NH}_{4}^{+}$ , which is similar to the general pattern in most areas of China and East Asia. However, at Zhuzhang (ZUZ, 28° 00′ N, 99° 43′ E, 3,583 m asl) in northwestern Yunnan Province, the aerosol concentrations and compositions showed little seasonal variation except for a decreasing trend of OC from August to autumn–winter. Additionally, the OC variations dominated the seasonal variation of PM₁₀ (particles ≤10 μm diameter) level. Chemical characteristics combined with transport information suggested sea salt origin of ionic Na^?+?, Mg^2?+?, and Cl^??? at ZUZ. At AKD, ionic Ca^2?+?, Mg^2?+?, Na^?+?, and Cl^??? primarily originated from salinized soil. Furthermore, the WS Ca^2?+? contributions (5.4–6%) to the PM₁₀ mass during autumn, winter, and early spring reflected a constant dust component. The results of this study indicated that both sites were regionally representative. However, the representative regions and scales of these background sites may vary seasonally as the regional atmospheric transport patterns change. Seasonal variations in the background aerosol levels from these two areas need to be considered when evaluating the regional climate effects of the aerosols.     

Impact of ultrasonic treatment on dewaterability of sludge during Fenton oxidation

Fenton oxidation was compared with Fenton oxidation coupled with ultrasonication (Fenton?+?US) for sludge dewatering. Different Fenton reagent (H₂O₂, Fe²⁺) concentrations, pH, and reaction times were studied in different systems on the basis of the specific resistance to filtration (SRF) and capillary suction time (CST). It was found that Fenton?+?US can significantly reduce Fe²⁺ and H₂O₂ dosages and reaction times. After ultrasonication of the system at pH 3, with an ultrasonic frequency of 25 kHz and a sound energy density of 100 W/L, the Fe²⁺, H₂O₂ dosage, and reaction time were reduced by 66.7, 75.0, and 75.0 %, respectively, when compared with Fenton oxidation at the same dewaterability of sludge. The microstructure of sludge and hydroxyl radical (·OH) density in Fenton oxidation and Fenton?+?US was further examined. Fenton?+?US produced more?·?OH in a sludge system than did individual Fenton oxidation. The concentration of?·?OH in Fenton?+?US fell from 79.2 to 6 mg/L over 3.5 h, while the concentration of?·?OH in Fenton oxidation fell from 59.6 to 1 mg/L over 2 h, thus destroying the microstructure of sludge more effectively. Sludge treated using Fenton?+?US for 30 min showed a much thinner and looser microstructure.     

Multiple metal tolerance and biosorption of cadmium by Candida tropicalis isolated from industrial effluents: glutathione as detoxifying agent

The ability of cadmium uptake by metal-resistant yeast, Candida tropicalis, from the liquid medium and wastewater was evaluated. The minimum inhibitory concentration of Cd^2?+? against C. tropicalis was 2,500 mg L^???1. The yeast also showed tolerance toward Zn^2?+? (1,400 mg L^???1), Ni^2?+? (1,000 mg L^???1), Hg^2?+? (1,400 mg L^???1), Cu^2?+? (1,000 mg L^???1), Cr^6?+? (1,200 mg L^???1), and Pb^2?+? (1,000 mg L^???1). The yeast isolate showed typical growth curves, but lag and log phases extended in the presence of cadmium. The yeast isolate showed optimum growth at 30°C and pH 8. The metal processing ability of the isolate was determined in a medium containing 100 mg L^???1 of Cd^2?+?. C. tropicalis could decline Cd^2?+? 70%, 85%, and 92% from the medium after 48, 96, and 144 h, respectively. C. tropicalis was also able to remove Cd^2?+? 40% and 78% from the wastewater after 6 and 12 days, respectively. Cd produced an increase in glutathione (GSH) and nonprotein thiol levels by 135% and 134% at 100-mg L^???1 concentration, respectively. An increase in the synthesis of GSH is involved in metal tolerance, and the presence of increasing GSH concentrations may be a marker for high metal stress in C. tropicalis. C. tropicalis, which is resistant to heavy metal ions and is adaptable to the local environmental conditions, may be employed for metal detoxification operations.     

石家庄市大气颗粒物元素组分特征分析

为研究石家庄市大气颗粒物的污染特征及其来源,于2013年4—5月在主城6区分别采集TSP、PM10和PM2.5颗粒物样品,利用ICP-MS分析其中的22种元素浓度。结果表明,石家庄市城区Ca、Fe元素在各粒径颗粒物中含量都较高,PM2.5中的S、K含量较高,PM10和TSP中Mg、Al的浓度相对较高。颗粒物的主要来源为燃煤尘、道路尘和建筑尘,TSP、PM10和PM2.5具有较好的统计相关性和同源性。     

Chemical speciation in waters influenced by lead–zinc metallurgical industry

The Lead–Zinc Company region, Kardjali city, Bulgaria, is known to be highly polluted with heavy metals from its pyrometallurgical activities. The polluted levels and the chemical speciation in surface natural waters in the region as well as in the wastewaters of the factory were investigated in January 2008 by application of monitoring studies, thermodynamic modeling, and interpretation in terms of the “softness–hardness” factor. It was found that the levels of trace metals pollution of surface waters were lower than the legislation limits for the regions with Pb and Zn production. The wastewater treatment facilities of the company were found to operate properly, and the quality of the cleaned waters in station Kar4 was comparable to the other surface waters studied (e.g., station Kar5). The trace metals were divided into three groups: (1) Fe^3?+? and Al^3?+?, being “hard” acids, existed in all the studied waters as hydroxy species Fe(OH) $_{2}^{+}$ , AlOH^2?+?, and Al(OH) $_{2}^{+}$ , followed by the phosphate species AlPO $_{4}^{0}$ and Al₂(OH)₂PO $_{4}^{+}$ ; (2) Mn^2?+?, Zn^2?+?, and Cd^2?+? being “soft” acids with crystal field stabilization energy (CFSE) = 0 were present in natural waters mainly as free Me^2?+? ions. Small concentrations of their MeSO $_{4}^{0}$ , MeCO $_{3}^{0}$ species, and of MeCl $_{2}^{0}$ (Me = Zn, Cd) species were also calculated. In the wastewaters, two more species [Me(SO $_{4})_{2}^{2-}$ and Me(SO $_{4})_{3}^{4-}$ ] of the softer Zn and Cd metals were also calculated; (3) Cu^2?+? and Pb^2?+?, as “soft” acids with CFSE $\ne $ 0 preferentially coordinated with softer CO $_{3}^{2-}$ ions and in natural waters existed mainly as MeCO $_{3}^{0}$ and PbHCO $_{3}^{+}$ , followed by free Me^2?+?ions and MeOH^?+?. In the wastewaters, MeSO $_{4}^{0}$ and Pb(SO $_{4})_{2}^{2-}$ species increased at the expense of the free Me^2?+? ions. The highest self-cleaning capability of natural waters was found with respect to Al and Fe, followed by Mn and Cd. The lowest corresponded to Pb, Cu, and Zn.