Airborne exposure to chemical substances in hairdresser salons

Several studies indicate health problems among hairdressers to be related to their chemical exposure at work. The purpose of this study was to describe the exposure of chemical compounds in the air of Spanish hairdresser salons, and to study differences between salons in central and suburban areas. Ten hairdresser salons were examined for two days, by recording number and type of customers, ventilation and size of salon. Both stationary and personal borne samples for organic compounds were collected, as well as stationary samples of ammonia. TVOC was calculated. Air temperature, relative humidity, CO and CO2 were logged for 48 h in each salon. Fifty-six personal and 28 stationary samples were analysed for organic compounds. Thirty-five different air-borne compounds were found in the working environment of the hairdressers. All levels were well below the limit values in Spain and USA, both for ammonia and organic compounds. TVOC ranged from 48.37 mg/m3 to 237.60 mg/m3, meaning that many salons had levels above suggested comfort values of 25. There were only minor differences in exposure between central and suburban salons. No salons had ventilation systems, and the CO2 was increasing during the day. The exposure was higher for several chemical compounds when hair dying was performed. Hairdressers were exposed to low air levels of a large number of chemical substances mostly related to work related to hair dying. There were no differences between exposure levels in salons in central and suburban areas.     

Lead and cadmium concentrations in shorebirds from the Yeongjong Island, Korea

This study presents concentration levels of pollutants (lead, and cadmium) in tissues (livers, kidneys, muscles, and bones) of shorebirds (Kentish Plovers (n = 5), Mongolian Plovers (n = 2), Dunlins (n = 6), Great Knots (n = 10), Terek Sandpipers (n = 10)) from Yeongjong Island, Korea in the East Asian–Australian migration flyways during the autumn migration in 1994–1995. Lead concentrations in livers, in kidneys, in muscles, and in bones were significantly different among shorebird species. Lead concentrations in livers of Kentish Plovers (4.76 ± 2.72 μg/wet g), Mongolian Plovers (2.05 μg/wet g), Dunlins (3.77 ± 1.07 μg/wet g), and Great Knots (4.27 ± 3.19 μg/wet g) were less than the toxic level, and lead concentrations in livers of Terek Sandpipers (1.20 ± 0.94 μg/wet g) were at the background level. Cadmium concentrations in livers, in kidneys, in muscles, and in bones did not vary among shorebirds, and concentrations of cadmium in livers and in kidneys were at background level (respectively, approximate 1 μg/wet g, approximate 2.67 μg/wet g) in all shorebird species. We suggest that interspecific differences of lead and cadmium concentrations were attributed to differences in exposure time and differences of diet, microhabitats in wintering ground. In livers and kidney of shorebirds from Yeongjong Island, lead and cadmium concentrations were higher than other locations previously reported.     

Effects of Cadmium (CdCl2) on development and hatching of eggs in European squid (Loligo vulgaris Lamarck, 1798) (Cephalopoda: Loliginidae)

This is the first study related to the effects of cadmium (Cd) on the development and hatching of eggs of Loligo vulgaris. The eggs were exposed to concentrations varying from 10 to 100,000 μg Cd/l for up to 1 month. During the study period natural sea water salinity (37 PSU), ambient temperature (ranging 16.5–21.5°C) and light conditions of 12-h light: 12-h dark for 744-h were used prior to the hatching. For 96-h, mortality rate of 100% of the eggs was found at cadmium concentration of 100,000 μg Cd/l, and the same mortality rate of the eggs were found at 1,000 and 10,000 μg Cd/l for 744-h and 696-h, respectively. Hatching took place between hours 456 and 576 in the control group and between hours 480 and 576 in 10 and 100 μg Cd/l groups. Total hatching rates were calculated to be 98.2 ± 1.6% for control group, 99.4 ± 0.6% for 10 μg Cd/l group and 98.6 ± 1.2% for 100 μg Cd/l group. Hatching successes were estimated as 69.5 ± 13.8% for control group, 84.5 ± 8.2% for 10 μg Cd/l group and 76.9 ± 5.9% for 100 μg Cd/l group. In the 100,000 μg Cd/l treatment, the egg degeneration began from animal pole of the eggs in 16 h, and 50% and 100% of them died in the initial stage at 72-h and 96-h, respectively. In the 10,000 μg Cd/l group, the eggs which reached at stage 19 (IX) were deformed and 50% and 100% of them died at 312-h and 696-h, respectively. In 1,000 μg Cd/l group, however, the eggs developed abnormally from stage 21 (X–XI) and reached at stage 29 (XIX), and 50% and 100% of them died in 624-h and in 744-h, respectively. There were significant differences in survival rates of the eggs among the concentrations (p < 0.05). The current study demonstrated that Cd adversely affects the development, survival and hatching of L. vulgaris eggs; however, no mortality was observed in 10 μg Cd/l and 100 μg Cd/l groups.     

Organochlorine pesticides and polychlorinated biphenyls in common buzzard (<Emphasis Type="Italic">Buteo buteo</Emphasis>) from Sicily (Italy)

In the present study, we investigated the concentrations and distribution of organochlorine pesticides (OCs) and polychlorinated biphenyls (PCBs) in intestine, liver, and muscle samples of 11 common buzzards (Buteo buteo) from Sicily used as bioindicator for monitoring pollution in environment. All samples of common buzzards were collected at the “Recovery Center of Wild Fauna” of Palermo, through the Zooprophilactic Institute. Quantitative determination of OCs and PCBs in the samples examined has been carried out using HRGC-ECD and GC-MS. The results obtained show the presence of concentrations of ∑DDT and ∑PCB in almost all samples. Regarding ∑DDT (4,4^′-DDE, 2,4^′-DDD, 4,4^′-DDD, 2,4^′-DDT, and 4,4^′-DDT), the highest concentrations were found in intestine (0.411 ± 0.050 μg/g) followed by muscle (0.130 ± 0.017 μg/g) and liver samples (0.109 ± 0.014 μg/g). As regards the ∑PCB congeners (PCB-28, PCB-52, PCB-95, PCB-99, PCB-101, PCB-110, PCB-138, PCB-146, PCB-149, PCB-151, PCB-153, PCB-170, PCB-177, PCB-180, PCB-183, and PCB-187), the highest concentrations were found in intestine (1.686 ± 0.144 μg/g) followed by liver (1.064 ± 0.162 μg/g) and muscle samples (0.797 ± 0.078 μg/g). Our data deserve particular attention not only for their significance but especially because they were recorded in Sicily, a region with a very low risk of environmental pollution due to the shortage of industries.     

Methyl mercury in fish—a case study on various samples collected from Ganges river at West Bengal

This study investigated the presence of total mercury (Hg) and organic mercury levels in the muscle of 19 common fresh water fish species captured from river Ganges, West Bengal, India. The total mercury level found in our study may not cause any toxic effect, but the methyl mercury (MeHg) level in some freshwater fish species was surprisingly very high and toxically unacceptable. The results of mercury analysis in various specimens indicated that some fish muscles tended to accumulate high levels of Hg, and approximately 50–84% of Hg was organic mercury. A strong positive correlation between mercury levels in muscle with food habit and fish length (age) was found. Wallago attu possessed the highest amount of organic mercury in their muscle tissues, and it was 0.93 ± 0.61 μg Hg/g of wet weight. Whereas in small-sized fishes Eutropiichthys murius, Puntius sarana, Cirrhinus mrigala, Mystus vittatus or Mystus gulio, and Tilapia mossambicus, it was below the detection limit. Contamination in Catla catla (0.32 ± 0.11), Anguilla bengalensis bengalensis (0.26 ± 0.07 μg Hg/g), Chitala chitala (0.25 ± 0.18), Rita rita (0.34 ± 0.14), and Ompok pabda (0.26 ± 0.04) was also above the 0.25 μg Hg/g of wet weight, the limit set by the PFA for the maximum level for consumption of fish exposed to MeHg. Though in Labeo rohita (0.12 ± 0.03), Mastacembelus armatus (0.17 ± 0.02), Pangasius pangasius (0.12 ± 0.16), Bagarius bagarius (0.12 ± 0.01), and Clupisoma garua (0.1 ± 0.01), concentration was below the recommended level, in Lates calcarifer (0.23 ± 0.0) and Mystus aor (0.23 ± 0.1), it was threatening. Interestingly, a low concentration of Hg was found in post-monsoon samples.     

Spatiotemporal distribution of arsineic species of oysters (Crassostrea gigas) in the coastal area of southwestern Taiwan

This study investigated total arsenic (As) and As species contents of oysters (Crassostrea gigas) in different production areas, seasons and sea locations on the southwestern coast of Taiwan. Analytical results indicate that contents of total As, arsenite, arsenate, dimethylarsinic acid, monomethylarsonic acid and arsenobetaine in oysters are 9.90 ± 3.68, 0.091 ± 0.104, 0.033 ± 0.038, 0.529 ± 0.284, 0.037 ± 0.046 and 3.94 ± 1.33 mg/g (dry wt), respectively. A ratio of inorganic As concentrations to total As concentrations is 1.26%. Total As contents of oysters cultured in the outer sea are statistically significantly lower than those of oysters cultured in the inner sea. The total As contents of oysters is the highest in Putai, where the blackfoot disease prevails. The low As contents in oysters is attributed to the low temperature in winter, which slows the metabolism of oysters. A maximum value is 33.37 μg/g (dry) in Putai in spring, because a considerable amount of aquacultural waste water with high As contents is discharged into adjacent drainage channels and rivers there during that season.     

Indoor and outdoor PM mass and number concentrations at schools in the Athens area

Simultaneous indoor and outdoor PM₁₀ and PM_2.5 concentration measurements were conducted in seven primary schools in the Athens area. Both gravimetric samplers and continuous monitors were used. Filters were subsequently analyzed for anion species. Moreover ultrafine particles number concentration was monitored continuously indoors and outdoors. Mean 8-hr PM₁₀ concentration was measured equal to 229 ± 182 μg/m³ indoors and 166 ± 133 μg/m³ outdoors. The respective PM_2.5 concentrations were 82 ± 56 μg/m³ indoors and 56 ± 26 μg/m³ outdoors. Ultrafine particles 8-h mean number concentration was measured equal to 24,000 ± 17,900 particles/cm³ indoors and 32,000 ± 14,200 particles/cm³ outdoors. PM₁₀ outdoor concentrations exhibited a greater spatial variability than the corresponding PM_2.5 ones. I/O ratios were close or above 1.00 for PM₁₀ and PM_2.5 and smaller than 1.00 for ultrafine particles. Very high I/O ratios were observed when intense activities took place. The initial results of the chemical analysis showed that accounts for the 6.6 ± 3.5% of the PM₁₀ and for the 3.1 ± 1.4%.The corresponding results for PM_2.5 are 12.0 ± 7.7% for and 3.1 ± 1.9% for . PM_2.5 indoor concentrations were highly correlated with outdoor ones and the regression line had the largest slope and a very low intercept, indicative of no indoor sources of fine particulate . The results of the statistical analysis of indoor and outdoor concentration data support the use of as a proper surrogate for indoor PM of outdoor origin.     

Determination of ametryn in sugarcane and ametryn–atrazine herbicide formulations using spectrophotometric method

A sensitive spectrophotometric method has been developed for determination of ametryn in agricultural samples. The proposed method was based on reaction with pyridine and further coupling with sulfanilic acid to form a colored product. The absorbance was measured at 400 nm with a molar absorptivity of 2.1 × 10⁵ L mol⁻¹ cm⁻¹. The method shows a linear range from 0.2–20 μg mL⁻¹ with limit of detection and limit of quantification 0.16 and 0.54 μg mL⁻¹, respectively. The method has been successfully applied to the determination of ametryn in sugarcane juice and commercial formulations after separation of ametryn from triazine herbicides based on solvent extraction. Recovery values were found to be in the range of 96.0 ± 0.2% to 98.4 ± 0.1%.     

Estimation of Polish cigarettes contamination with cadmium and lead, and exposure to these metals via smoking

To estimate exposure to cadmium (Cd) and lead (Pb) through cigarette smoking, the concentrations of both metals in the blood or/and urine of smokers (20 cigarettes or more per day for 10 years or longer) and their non-smoking counterparts inhabiting an environmentally unpolluted area (Bialystok, Poland) were evaluated, as well as Cd and Pb contents in the cigarette brands (produced in Poland) smoked by the participants, including intact cigarettes, pre-smoking (tobacco, paper and filter) and post-smoking (butt, ash and smoke) cigarette components. Blood and urinary Cd concentrations in the smokers have been already reported by us to be 2–4 times higher than in the non-smokers (Galażyn-Sidorczuk et al. Polish Journal of Environmental Studies, 13 (Suppl.1):91–95, 2004). All the other measurements are the subject of the present paper. Pb concentration in the blood of the cigarette smokers (52.12 ± 15.51 μg l⁻¹) was higher by 29% than in the non-smokers (40.42 ± 11.19 μg l⁻¹). The mean Cd and Pb contents in the cigarettes were 0.6801 ± 0.1765 and 0.6853 ± 0.0746 μg per cigarette, respectively. Under cigarette burning, performed using a machine for self-acting burning, on average 33% of Cd and 11% of Pb present in the whole cigarette was released into the smoke. For Cd, unlike Pb, there was a high positive correlation between the metal content in cigarettes and tobacco and its release into the smoke. Moreover, the subjects smoking cigarettes containing the highest Cd amount had higher blood Cd concentration than smokers of other cigarette brands. The results give clear evidence that in the case of inhabitants of areas unpolluted with Cd and Pb habitual cigarette smoking, due to tobacco contamination, creates a serious source of chronic exposure to these metals, especially to Cd.     

A spectrophotometric assay method for vanadium in biological and environmental samples using 2,4-dinitrophenylhydrazine with imipramine hydrochloride

A simple, rapid, and sensitive method involving the interaction of 2,4-dinitrophenylhydrazine with imipramine hydrochloride in presence of vanadium (V) in sulfuric acid medium has been proposed for the determination of vanadium. The purple-colored product developed showed an absorption maximum at 560 nm and was stable for 24 h. The working curve was linear over the concentration range of 0.1–2.8 μg ml^− 1, with sensitivity of detection of 0.0124 μg ml^− 1. Molar absorptivity and Sandell’s sensitivity were found to be 2.6 × 10⁴ l/mol cm and 0.0039 μg cm^− 1, respectively. The accuracy of the proposed method was assessed by Student’s t test and variance ratio F test, and the results were on par with the reported method. The method was successfully used in the determination of V in water, human urine, soil, and plant samples, and it was free from interference by various concomitant ions.     

The statistical investigation on airborne fungi and pollen grains of atmosphere in Izmir-Turkey

This study aims to investigate the differences in the concentrations of airborne fungi and pollens between the towns located in the province of Izmir and to determine the factors contributing to these differences. Five stations in each of four towns (Buca, Konak, Bornova, and Karsiyaka) were randomly selected as the research areas. Fungus (cfu/m³) and pollen counts (cm²/pollen count) in the air samples collected from each station between June 2003 and May 2004 were measured. The results revealed that whereas Karsiyaka had the highest fungus concentration (521.33 ± 777.1), Buca and Bornova had the lowest concentration (482.67 ± 308.44). The mean fungus concentration in the province of İzmir was 501.5 ± 486.7. Pollen concentration was the highest in Konak (486.67 ± 839.06) and the lowest in Bornova (369.83 ± 551.13). Fungus and pollen concentrations revealed no difference between the towns (p > 0.05). The relationship between pollen-fungus concentrations and temperature-dust-humidity-sulphurdioxide was investigated but it was found statistically insignificant (p > 0.05). As a result of regression analysis, it was determined that correlation of atmospheric parameters had no effects on pollen and fungus concentrations (p > 0.05).     

Rinodina sophodes (Ach.) Massal.: a bioaccumulator of polycyclic aromatic hydrocarbons (PAHs) in Kanpur City, India

The aim of this study is to determine the possibility of using Rinodina sophodes (Ach.) Massal., a crustose lichen as polycyclic aromatic hydrocarbons (PAHs) bioaccumulator for evaluation of atmospheric pollution in tropical areas of India, where few species of lichens are able to grow. PAHs were identified, quantified and compared to evaluate the potential utility of R. sophodes. The limit of detection for different PAHs was found to be 0.008–0.050 μg g^− 1. The total PAHs in different sites were ranged between 0.189 ± 0.029 and 0.494 ± 0.105 μg g^− 1. The major sources of PAHs were combustion of organic materials, traffic and vehicular exhaust (diesel and gasoline engine). Significantly higher concentration of acenaphthylene and phenanthrene indicates road traffic as major source of PAH pollution in the city. Two-way ANOVA also confirms that all PAHs content showed significant differences between all sampling sites (P 1%). This study establishes the utility of R. sophodes in monitoring the PAHs accumulation potentiality for development of effective tool and explores the most potential traits resistant to the hazardous environmental conditions in the tropical regions of north India, where no such other effective way of biomonitoring is known so far.     

The determination of ambient formaldehyde using a dual coil system and an assessment of dominant factors that influence its abundance in Korea

An enhanced dual coil 2,4-dinitrophenylhydrazine (DNPH) derivatization method (dual coil/DNPH) allowed the quantitative determination of formaldehyde (HCHO) in ambient air. In this method, traceable HCHO was collected using a coil sampler connected in series and lacking a long sampling tube. It was then analyzed using liquid chromatography followed by UV detection of the DNPH derivatives. The method is based on the reaction of formaldehyde with DNPH to produce 2,4-dinitrophenylhydrazone. The detection limits (3σ) were 0.10–0.40 ppbv with a precision ranging from 0.84 to 4.09% RSD. The results of dual coil/DNPH and conventional DNPH cartridge methods were generally well correlated: HCHO (dual coil/DNPH) = 0.97 (±0.13) vs. HCHO (DNPH Cartridge) + 0.33 (±0.33), r = 0.82. The dual coil/DNPH method was used to measure gaseous HCHO in the atmosphere of Metropolitan Seoul during the summer 2000 and 2001, and in Gwangju during the fall of 2001 and 2002. The daytime mean concentration of HCHO was 4.52 (±5.69) and 3.21 (±1.27) ppbv in Metropolitan Seoul for 10–12 August 2000 and 29–31 May 2001, respectively, and 1.73 (±0.98), 3.04 (±2.25), 2.70 (±1.70), and 2.01 (±2.28) ppbv in Gwangju City during 22–27 September 2001, 17–24 October 2001, 9–13 October 2002, and 28 October to 2 November 2002, respectively. The HCHO in Seoul from 10–12 August 2000 was mainly the result of photochemical processes, while direct emissions from vehicles and long-range transport of air from China contributed during 29–31 May 2001. During 22–27 September 2001, 17–24 October 2001, and 9–13 October 2002 in Gwangju, the HCHO came primarily from photochemical processes, although some air affected by biomass burning admixed in the late afternoon. The increase in the HCHO concentration on 20 October 2001 and from 28 October to 2 November 2002 was attributed mainly to direct emissions from biomass burning in farmland near the measurement site.     

Aerosol characteristics and surface radiative forcing components during a dust outbreak in Gwangju, Republic of Korea

Atmospheric surface aerosol radiative forcing (SARF) ΔF, forcing efficiency ΔF_e and fractional forcing efficiency ΔFF_e evaluated from cloud-screened narrowband spectral and thermal-offset-corrected radiometric observations during the Asia dust outbreak episodes in Gwangju, Republic of Korea are reported in this study. Columnar aerosol optical properties (aerosol optical depth (AOD), τ _aλ, Angstrom exponent α, mass concentration of fine and coarse mode particles) were also reported for the station between January 2000 and May 2001 consisting of 211cloud-free days. Results indicate that majority of the AOD were within the range 0.25–0.45 while some high aerosol events in which AODs ≥ 0.6 were observed during the severe dust episodes. For example, AOD increases from annual average value of 0.34 ± 0.13 at 501 nm to values >0.60 during the major dust events of March 27–30 and April 7–9, 2000, respectively. The α _{501–870 nm} which is often used as a qualitative indicator of aerosol particle size had values ranging from 0.01 to 1.77. The diurnal forcing efficiency ΔDF_e at Gwangju was estimated to be −81.10 ± 5.14 W m ⁻²/τ _{501 nm} and −47.09 ± 2.20 W m ⁻²/τ _{501 nm} for the total solar broadband and visible band pass, respectively while the fractional diurnal forcing efficiency ΔFDF_e were −15.8 ± 0.64%/τ _{501 nm} and −22.87 ± 1.13%/τ _{501 nm} for the same band passes. Analyses of the 5-day air-mass back trajectories were further developed for Gwangju in order to classify the air-mass and types of aerosol reaching the site during the Asia dust episodes.     

Selective and sensitive extractive spectrophotometric determination of micro amounts of palladium(II) in spiked samples: using a new reagent N-ethyl-3-carbazolecarbaxaledehydethiosemicarbazone

N-Ethyl-3-cabazolecarboxaldehydethiosemicarbazone (ECCT) is proposed as a new, sensitive and selective complexing reagent for the separation and extractive spectrophotometric determination of palladium(II) at pH: 4.0 to form a yellowish orange colored 1:1 chelate complex, which is very well extracted in to n-butanol. The absorbance was measured at a maximum wavelength, 410 nm. This method obeys Beer’s law in the concentration range 0.0–6.6 μg mL⁻¹ and the correlation coefficient of Pd(II)-ECCT complex is 0.998, which indicates an excellent linearity between the two variables with good molar absorptivity and Sandell’s sensitivity, 1.647 × 10⁴ l mol⁻¹cm⁻¹, 6.49 × 10⁻³ μg cm⁻², respectively. The instability constant of complex calculated from Edmond’s method, 2.724 × 10⁻⁵ was in good agreement with the value calculated from Asmus’ method 2.624 × 10⁻⁵, at room temperature. The precision and accuracy of the method is checked with calculation of relative standard deviation (n = 5), 0.839. Edmond’s method was observed to be a more selective method in the presence of EDTA, oxalate and phosphate ions. The method was successfully applied for the determination of Pd(II) in water samples, synthetic mixtures and hydrogenation catalysts, employing an atomic absorption spectrometer for comparing these results.     

Study of metals concentration levels in Patella piperata throughout the Canary Islands, Spain

In order to assess the extent of metal contamination at rocky shores of the Canarian Archipelago, metal concentrations have been measured in Patella piperata (Gould, 1846), using the standard atomic absorption spectrophotometer technique. Ranges of elements concentrations measured (in μg g⁻¹) found in the biota were: Cd (0.36 ± 0.26 μg g⁻¹ dry wt.), Cu (2.05 ± 0.91 dry wt.), Pb (1.57 ± 1.14 μg g⁻¹dry wt.) and Zn (10.37 ± 4.60 μg g⁻¹ dry wt.). Variation in metal concentrations in Patella, was tested by using non-parametric statistical methods. Cd content had a maximum in the Archipelago Chinijo, northward of Lanzarote Island. The metal concentrations recorded at the clean stations may be considered carefully if they are used like background levels.     

Risk assessment due to intake of heavy metals through the ingestion of groundwater around two proposed uranium mining areas in Jharkhand,India

Heavy metal pollution of water resources can be apprehended in East Singhbhum region which is a highly mineralised zone with extensive mining of copper, uranium and other minerals. Ten groundwater samples were collected from each site and the heavy metal analysis was done by atomic absorption spectrophotometer. Analysis of the results of the study reveals that the concentration of iron, manganese, zinc, lead, copper and nickel in groundwater of Bagjata mining area ranged 0.06–5.3 mg l^− 1, 0.01–1.3 mg l^− 1, 0.02–8.2 mg l^− 1, 1.4–28.4 μg l^− 1, 0.78–20.0 μg l^− 1 and 1.05–20.1 μg l^− 1, respectively. In case of Banduhurang mining area, the range was 0.04–2.93 mg l^− 1, 0.02–1.1 mg l^− 1, 0.01–4.68 mg l^− 1, 1.04–33.21 μg l^− 1, 1.24–18.7 μg l^− 1 and 1.06–14.58 μg l^− 1, respectively. The heavy metals were found to be below the drinking water standards (IS:10500 1993) except iron (0.3 mg l^− 1) and manganese (0.1 mg l^− 1). The hazard quotients of the heavy metals for drinking water were below 1 posing no threat due to intake of water to the people for both the areas.     

Evaluation of levels, sources and distribution of toxic elements in PM10 in a suburban industrial region, Rio de Janeiro, Brazil

The Oswaldo Cruz Foundation Campus (FIOCRUZ), in a suburban region of the city of Rio de Janeiro, was selected as a case study to assess the pollution released from vehicle and industrial facilities in Basin III, the most polluted area of the city. Concentrations of particulate matter (PM10) and trace metals in airborne particles were determined in an intensive field campaign. The samplings were performed every six days for 24 h periods, using a PM10 high volume sampler, from September 2004 to August 2005. PM10 mass concentrations were determined gravimetrically and the metals by ICP-OES. For PM10, the arithmetic mean for the period is 169 ± 42 μg m⁻³ which is 3.4 times the national recommended standard of 50 μg m⁻³. Additionally, 51% of the samplings exceeded the recommended 24 h limit of 150 μg m⁻³. Ca, Mg, Fe, Zn and Al were the metals that presented the higher concentrations. The correlation matrix gave two main clusters and three significant principal components (PC). Both PC1 and PC2 are associated to crustal, vehicular and industrial emissions while PC3 is mainly associated to geological material. Enrichment factors for Zn, Cu, Cd and Pb indicate that for these elements, anthropic sources prevail over natural inputs. PM10 levels showed a good correlation with hospital admissions for respiratory diseases in children and elderly people.     

Varying Stable Nitrogen Isotope Ratios of Different Coastal Marsh Plants and Their Relationships with Wastewater Nitrogen and Land Use in New England, USA

The stable nitrogen isotope ratios of some biota have been used as indicators of sources of anthropogenic nitrogen. In this study the relationships of the stable nitrogen isotope ratios of marsh plants, Iva frutescens (L.), Phragmites australis (Cav.) Trin ex Steud, Spartina patens (Ait.) Muhl, Spartina alterniflora Loisel, Ulva lactuca (L.), and Enteromorpha intestinalis (L.) with wastewater nitrogen and land development in New England are described. Five of the six plant species (all but U. lactuca) showed significant relationships of increasing δ ¹⁵N values with increasing wastewater nitrogen. There was a significant (P < 0.0001) downward shift in the δ ¹⁵N of S. patens (6.0 ± 0.48‰) which is mycorrhizal compared with S. alterniflora (8.5 ± 0.41‰). The downward shift in δ ¹⁵N may be caused by the assimilation of fixed nitrogen in the roots of S. patens. P. australis within sites had wide ranges of δ ¹⁵N values, evidently influenced by the type of shoreline development or buffer at the upland border. In residential areas, the presence of a vegetated buffer (n = 24 locations) significantly (P < 0.001) reduced the δ ¹⁵N (mean = 7.4 ± 0.43‰) of the P. australis compared to stands where there was no buffer (mean = 10.9 ± 1.0‰; n = 15). Among the plant species, I. frutescens located near the upland border showed the most significant (R ² = 0.64; P = 0.006) inverse relationship with the percent agricultural land in the watershed. The δ ¹⁵N of P. australis and I. frustescens is apparently an indicator of local inputs near the upland border, while the δ ¹⁵N of Spartina relates with the integrated, watershed-sea nitrogen inputs.