Concentrations of particulates in ambient air,gaseous elementary mercury (GEM), and particulate-bound mercury (Hg(p)) at a traffic sampling site: a study of dry deposition in daytime and nighttime

In this investigation, the concentrations of particles in ambient air, gaseous elemental mercury (GEM), and particulate-bound mercury (Hg(p)) in total suspended particulates (TSP) as well as dry deposition at a (Traffic) sampling site at Hung-kuang were studied during the day and night in 2012. The results reveal that the mean concentrations of TSP in ambient air, GEM, and Hg(p) were 69.72 μg/m³, 3.17, and 0.024 ng/m³, respectively, at the Hung-kuang (Traffic) sampling site during daytime sampling periods. The results also reveal that the mean rates of dry deposition of particles from ambient air and Hg(p) were 145.20 μg/m² min and 0.022 ng/m² min, respectively, at the Hung-kuang (Traffic) sampling site during the daytime sampling period. The mean concentrations of TSP in ambient air, GEM, and Hg(p) were 60.56 μg/m³, 2.74, and 0.018 ng/m³, respectively, at the Hung-kuang (Traffic) sampling site during the nighttime sampling period. The mean rates of dry deposition of particles and Hg(p) from ambient air were 132.58 μg/m² min and 0.016 ng/m² min, respectively, at the Hung-kuang (Traffic) sampling site during the nighttime sampling period.     

Ambient air particulates and particulate-bound mercury Hg(p) concentrations: dry deposition study over a Traffic,Airport, Park (T.A.P.) areas during years of 2011–2012

The main purpose of this study was to monitor ambient air particles and particulate-bound mercury Hg(p) in total suspended particulate (TSP) concentrations and dry deposition at the Hung Kuang (Traffic), Taichung airport and Westing Park sampling sites during the daytime and nighttime, from 2011 to 2012. In addition, the calculated/measured dry deposition flux ratios of ambient air particles and particulate-bound mercury Hg(p) were also studied with Baklanov & Sorensen and the Williams models. For a particle size of 10 μm, the Baklanov & Sorensen model yielded better predictions of dry deposition of ambient air particulates and particulate-bound mercury Hg(p) at the Hung Kuang (Traffic), Taichung airport and Westing Park sampling site during the daytime and nighttime sampling periods. However, for particulates with sizes 20–23 μm, the results obtained in the study reveal that the Williams model provided better prediction results for ambient air particulates and particulate-bound mercury Hg(p) at all sampling sites in this study.

     

Trace element concentration in fine particulate matter (PM<Subscript>2.5</Subscript>) and their bioavailability in different microenvironments in Agra,India: a case study

Exposure to airborne particulate matter results in the deposition of millions of particle in the lung; consequently, there is need for monitoring them particularly in indoor environments. Case study was conducted in three different microenvironments, i.e., urban, rural and roadside to examine the elemental bioavailability in fine particulate matter and its potential health risk. The samples were collected on polytetrafluoroethylene filter paper with the help of fine particulate sampler during August–September, 2012. The average mass concentration of PM_2.5 was 71.23 µg m^?3 (rural), 45.33 µg m^?3 (urban) and 36.71 µg m^?3 (roadside). Elements in PM_2.5 were analyzed by inductively coupled plasma atomic emission spectroscopy. Percentage bioavailability was determined to know the amount of soluble fraction that is actually taken across the cell membrane through inhalation pathway. Cadmium and lead were found to have cancer risk in a risk evaluation using an Integrated Risk Information system.     

Metal characterization of airborne particulate matters in a coastal region

The concentrations of suspended particulate matter in the air of the Orissa Sand Complex had an average value of 128 ± 10 µg m^?3 in residential areas and 170 ± 8 µg m^?3 in mining areas. PM₁₀ levels in residential areas were found to have an average of 35 ± 10 µg m^?3, in mining areas 45 ± 10 µg m^?3. The distribution of some elements is also discussed here. Inhalation doses were observed to be higher in summer than in winter and the rainy season. The highest dose rate was for the age group of 1 year, and health risks were found to be highest for the same. For adults, inhalation dose and health risk are 1.3 times higher in mining than in residential areas.     

Atrazin

Atmospheric occurrence and deposition of atrazine are measured. During the application of atrazine, highest concentrations reached 1.6 μg·1^?1 in liquid water of lowlying clouds touching mountain tops. Atmospheric deposition, however, hardly amounts to 0.4% of the flux on crop land by direct spraying. Airborne concentrations ranged from less than 0.005 ng·m^?3 to 0.32 ng·m^?3. Contrary to theoretical expectations, almost all atrazine was found in the particulate matter, indicating nonequilibrium with the gas phase. This may inhibit a rapid photochemical decomposition. Human health concerns and environmental risks due to the atmospheric occurrence and deposition of atrazine are judged as minor. This conclusion can be applied to many other, physicochemically related pesticides.     

Elemental composition of particulate matters around Urmia Lake,Iran

Atmospheric particulate matters and their elements were concurrently measured at two sites located in the north and southeast parts of Urmia Lake from January to September 2013. At both sampling sites, average concentrations of total suspended particulate, particles with the aerodynamic diameter of smaller than 10 µm, smaller than 2.5 µm, and smaller than 1 µm were 260 ± 106, 180 ± 73, 30 ± 8, and 25 ± 7 µg m^?3, respectively. The analyzed water soluble ions accounted for approximately 11%–13% mass concentrations of total suspended particulate and 8%–9% of particles smaller than 10 µm, and the sum of the concentrations of the analyzed elements associated with both ranged from 9 to 41 µg m^?3 (6.5%–9.6% in mass) and 7 to 26 µg m^?3 (5.5%–11.3% in mass), respectively. Thus, particulate matter was composed of a complex mixture of minerals such as halite, quartz, gypsum, hexahydrite, and Bassanite.     

Source identification of particulate matter and associated intake of elements through inhalation in an industrial area of Odisha,India

Particulate matter concentrations were measured in an industrial region in the Ganjam district of Odisha. The average levels of suspended particulate matter (SPM) were measured to be 142 ± 8 and PM₁₀ of particulate matter with a size of less than 10 micrometers (PM₁₀) to be 50 ± 15 μg m^?3. Out of the 14 elements determined, Ca, Na, Mg, Fe, and K contributed more than 95% of the total weight. In enrichment factors, the trace elements, i.e., Zn, Pb, Cd, and Hg were observed to be highly enriched in the SPM and PM₁₀. Factor analysis indicates that more than 75% of the variance was due to five component factors, which have eigenvalues greater than 1. Intake of elements through inhalation route to adults has been estimated.     

Environmental impact of CO<Subscript>2</Subscript>, Rn,Hg degassing from the rupture zones produced by Wenchuan <Emphasis Type="Italic">M</Emphasis><Subscript>s</Subscript> 8.0 earthquake in western Sichuan,China

The concentrations and flux of CO₂, ²²²Radon (Rn), and gaseous elemental mercury (Hg) in soil gas were investigated based on the field measurements in June 2010 at ten sites along the seismic rupture zones produced by the May 12, 2008, Wenchuan M _s 8.0 earthquake in order to assess the environmental impact of degassing of CO₂, Rn and Hg. Soil gas concentrations of 344 sampling points were obtained. Seventy measurements of CO₂, Rn and Hg flux by the static accumulation chamber method were performed. The results of risk assessment of CO₂, Rn and Hg concentration in soil gas showed that (1) the concentration of CO₂ in the epicenter of Wenchuan M _s 8.0 earthquake and north end of seismic ruptures had low risk of asphyxia; (2) the concentrations of Rn in the north segment of seismic ruptures had high levels of radon, Maximum was up to level 4, according to Chinese code (GB 50325-2001); (3) the average geoaccumulation index I _geo of soil Hg denoted the lack of soil contamination, and maximum values classified the soil gas as moderately to strongly polluted in the epicenter. The investigation of soil gas CO₂, Rn and Hg degassing rate indicated that (1) the CO₂ in soil gas was characterized by a mean \(\updelta^{13}C_{CO2}\) of ?20.4 ‰ and by a mean CO₂ flux of 88.1 g m^?2 day^?1, which were in the range of the typical values for biologic CO₂ degassing. The maximum of soil CO₂ flux reached values of 399 g m^?2 day^?1 in the epicenter; (2) the soil Rn had higher exhalation in the north segment of seismic ruptures, the maximum reached value of 1976 m Bq m^?2 s^?1; (3) the soil Hg flux was lower, ranging from ?2.5 to 18.7 n g m^?2 h^?1 and increased from south to north. The mean flux over the all profiles was 4.2 n g m^?2 h^?1. The total output of CO₂ and Hg degassing estimated along seismic ruptures for a survey area of 18.17 km² were approximately 0.57 Mt year^?1 and 688.19 g year^?1. It is recommended that land-use planners should incorporate soil gas and/or gas flux measurements in the environmental assessment of areas of possible risk. A survey of all houses along seismic ruptures is advised as structural measures to prevent the ingress of soil gases, including CO₂ and Rn, were needed in some houses.     

High seasonal variation of atmospheric C and particle concentrations in Delhi,India

The highly populated Indian regions are currently in a phase of rapid economic growth resulting in high emissions of carbonaceous aerosols. This leads to poor air quality and impact on climate. The chemical composition of carbonaceous aerosols has rarely been studied in industrial areas of India. Here, we investigated carbonaceous aerosols in particulate matter (PM) monthly in the industrial area of Delhi in 2011. The concentrations of organic C and elemental C in PM₁₀ fraction were analyzed. Results show a clear seasonal variability of organic and elemental C. PM₁₀ ranged 95.9–453.5 μg m^?3, organic C ranged 28.8–159.4 μg m^?3, and elemental C ranged 7.5–44.0 μg m^?3; those values were higher than reported values. Organic and elemental C were correlated with each other in pre-monsoon and winter seasons, implying the existence of similar emission sources such as coal combustion, biomass burning and vehicular exhaust. The annual average contribution of total carbonaceous aerosols in PM₁₀ was estimated as 62 %.     

Characteristics,sources and health risk assessment of toxic heavy metals in PM<Subscript>2.5</Subscript> at a megacity of southwest China

Twenty trace elements in fine particulate matters (i.e., PM_2.5) at urban Chengdu, a southwest megacity of China, were determined to study the characteristics, sources and human health risk of particulate toxic heavy metals. This work mainly focused on eight toxic heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The average concentration of PM_2.5 was 165.1 ± 84.7 µg m^?3 during the study period, significantly exceeding the National Ambient Air Quality Standard (35 µg m^?3 in annual average). The particulate heavy metal pollution was very serious in which Cd and As concentrations in PM_2.5 significantly surpassed the WHO standard. The enrichment factor values of heavy metals were typically higher than 10, suggesting that they were mainly influenced by anthropogenic sources. More specifically, the Cr, Mn and Ni were slightly enriched, Cu was highly enriched, while As, Cd, Pb and Zn were severely enriched. The results of correlation analysis showed that Cd may come from metallurgy and mechanical manufacturing emissions, and the other metals were predominately influenced by traffic emissions and coal combustion. The results of health risk assessment indicated that As, Mn and Cd would pose a significant non-carcinogenic health risk to both children and adults, while Cr would cause carcinogenic risk. Other toxic heavy metals were within a safe level.     

Arsenic concentration in rice, fish, meat and vegetables in Cambodia: a preliminary risk assessment

To assess arsenic contaminations and its possible adverse health effects, food samples were collected from Kandal, Kratie and Kampong Cham in Cambodia. The highest and the lowest concentrations were observed in fish (mean 2,832 ng g^?1, ww) collected from Kandal province and cattle stomach (1.86 ± 1.10 ng g^?1, ww) collected from Kratie, respectively. The daily intake of arsenic via food consumption was 604, 9.70 and 136 μg day^?1 in Kandal, Kratie and Kampong Cham, respectively. The arsenic dietary intake in Kandal ranked No. 1 among all the 17 compared countries or regions. Fish consumption contributed the greatest proportion of total arsenic daily intake in Kandal (about 63.0 %) and Kampong Cham (about 69.8 %). It is revealed to be a much more important exposure pathway than drinking water for residents in Kampong Cham. The results of risk assessment suggested that the residents in Cambodia, particularly for people in Kandal province, suffer high public health risks due to consuming arsenic-contaminated food.     

Distribution,sources and potential risk of HCH and DDT in soils from a typical alluvial plain of the Yangtze River Delta region,China

Spatial distribution, sources and potential health risks of organochlorine pesticides (OCPs), including hexachlorocyclohexane (HCH) and dichlorodiphenyltrichloroethane (DDT), in surface soils (n = 544) collected from a typical alluvial plain of the Yangtze River Delta region, China, were elucidated. Concentrations of ΣHCH and ΣDDT in soils ranged from less than the limit of detection (<LOD) to 99.0 ng g^?1, dry weight (dw) (mean 3.23 ng g^?1 dw) and <LOD to 600 ng g^?1 dw (mean 88.8 ng g^?1 dw), respectively. Historical applications of HCH and DDT were the major sources of the residue in soils. HCH was mainly distributed in Anthrosols in the southern part of the watershed, while DDT was mainly distributed in Cambosols in the northern part. The 95 % cumulative probability incremental lifetime cancer risks (ILCRs) of different age groups such as children, youths, and adults all exceeded the acceptable risk level of 10^?6 recommended by USEPA for carcinogenic chemicals. The spatial distributions of ∑ILCRs were consistent with concentrations of OCPs in soils, while they were slight different for the different age groups. Adult females had the greatest risk of OCPs in soils, followed by children, while youths had the least risk. The ingestion of OCPs in soils was the more important route of exposure compared with dermal and inhalation exposures. The concentration of OCPs in soils, the particulate emission factor, the fraction of dermal exposure ratio, and the soil ingestion rate were the major contributing variables to total ILCRs according to sensitivity analyses.     

PAHs in organic film on glass window surfaces from central Shanghai,China: distribution,sources and risk assessment

Polycyclic aromatic hydrocarbons (PAHs) concentrations were analysed in the organic film on the glass surfaces of different functional areas in central Shanghai. Concentration levels of total PAHs in the organic film ranged from 1,348.5 to 4,007.9 ng m^?2. The concentration of PAHs was lowest in parks and green spaces (1,348.5 ng m^?2) and highest in traffic zones (4,007.9 ng m^?2). A concentration gradient of total PAHs was observed as follows: traffic zones > commercial areas > cultural and educational areas > parks and green spaces. The distribution of PAHs was characterised by 3–4 ring PAHs in the study areas. The most abundant PAHs were phenanthrene (20.5 %), fluorene (16.7 %), pyrene (12.4 %) and chrysene (Chry) (11.2 %). The mass of the bulk film was composed of organic and inorganic compounds and ranged from 246 to 1,288 mg m^?2. The bulk film thickness varied from 144 to 757 nm in the different functional areas. The ratios of An/178 and Fl/202 and principal component analysis suggested that PAHs came mainly from the mixed sources of fossil fuel, coal and incomplete combustion of biomass. Benzo[a]anthracene (BaA)/Chry is not suitable for use as a tracer for the transmission process of PAHs because of the rapid depletion of BaA in the organic film by photooxidation during daylight hours. The concentration of benzo[a]pyrene equivalent (BaPeq) varied from 21 to 701 ng g^?1, and the major carcinogenic contributors of the 16 PAHs were BaP, DahA, B[b/k]F and InP, accounting for 83 % of BaPeq.     

Heavy metals in the polychaete Glycera longipinnis from the southwest of India

Metal concentrations in sediment and in whole tissue of the benthic polychaete Glycera longipinnis collected along the southwest coast of India were analysed. Relative seasonal accumulation of metals (Cu, Pb, Cr, Ni, Zn, Cd, Hg) was studied by categorising the habitat as less polluted or highly polluted based on metal contamination routed through industrial and urban sources. The metal content in tissues varied seasonally in the ranges, Cu: 2.21–27.08 μg·g^?1, Pb: 0.06–4.92 μg·g^?1, Cr: 1.73–29.20 μg·g^?1, Ni: 1.60–4.61 μg·g^?1, Zn: 14.72–82.30 μg·g^?1, Cd: 0.04–1.38 μg·g^?1and Hg: below decetable limits to 0.86 μg·g^?1. Concentration of heavy metals was found to be high in the whole body of G. longipinnis pooled from the polluted transects. The results of this study suggest that G. longipinnis may act as a useful biological indicator for heavy metal pollution along the southwest coast of India.     

Measurement of indoor radon concentration and assessment of doses in different districts of Alexandria city, Egypt

The main objective of this study is to assess the health hazard due to the indoor radon. Measurement studies have been carried out in 56 dwellings belonging to 14 residential areas in Alexandria city, Egypt. Results are obtained using the LR-115 (Type II) alpha track detector in “closed-can” geometry. The dosimeters were installed in bedroom, living room, and the kitchens of each house. For intercomparison purpose, dosimeters are installed in basements, ground floor, and first floor. Measured indoor radon concentrations were found to vary from 15 to 132 Bq m^?3. The average radon concentrations in living room, bedrooms, and kitchen in basements were found to vary from to be 39 ± 10, 63 ± 15 and 81 ± 25 Bq m^?3, respectively. In living room, bedrooms, and kitchen, on ground floor, the average radon concentrations were found to be 35 ± 9, 44 ± 6 and 56 ± 10 Bq m^?3, whereas on first floor, the average values are 29 ± 8, 34 ± 7 and 45 ± 8 Bq m^?3, respectively. The overall mean radon concentration in all surveyed districts has been found to be 44 ± 16 Bq m^?3. The mean annual estimated effective dose received by the residents of the studied area is estimated to be 0.75 mSv. The obtained results are compared with the indoor radon levels prescribed by the International Commission on Radiation Protection and are found to be less than the action level recommended.     

Occurrence of benzotriazoles (BTRs) in indoor air from Albany,New York,USA, and its implications for inhalation exposure

Despite the widespread use of benzotriazoles as corrosion inhibitors in many household goods, studies on the occurrence of these compounds in indoor air are scarce. In this study, five benzotriazole derivatives were measured in 83 indoor air samples collected from various locations in Albany, New York, USA. Benzotriazoles were found in a majority of the indoor air samples, and the concentrations of their sum in bulk (vapor plus particulate phases) indoor air ranged from below the method limit of quantification to 492 ng·m^?3 (geometric mean: 5.8 ng·m^?3). The highest geometric mean concentration was found in air samples collected in parking garages (155 ng·m^?3), followed by barbershops (13.6), public places (11.5), auto repair shops (5.2), automobiles (4.5), homes (4.5), offices (3.7), and laboratories (2.8). Inhalation exposure to benzotriazoles was calculated on the basis of the measured geometric mean concentrations and air inhalation rate. The highest exposure dose was found for teenagers, with a geometric mean inhalation exposure dose of 79 ng·day^?1. The body-weight normalized exposure dose, however, was the highest for infants, at 3.2 ng·(kg bw)^?1·day^?1.     

Polychlorinated biphenyl (PCB) residues in European roe deer (Capreolus capreolus) and red deer (Cervus elaphus) from north-western Poland

The purpose of this study was to evaluate polychlorinated biphenyls (PCBs) contamination levels in roe and red deer from north-western Poland and to assess environmental pollution in this area. A quantitative analysis was conducted using a capillary gas chromatography/mass spectrometry method. The mean concentrations of ΣPCBs (sum of PCBs: 28, 52, 101, 138, 153, 180) in liver samples were 30.24±12.35 ng·g^?1 of lipid weight (l.w.) in roe deer and 60.13±14.23 ng·g^?1 l.w. in red deer, compared with 24.21±10.02 and 45.22±9.77 ng·g^?1 in the lungs of roe and red deer, respectively. PCBs 138, 153 and 180 were the dominant congeners in the liver samples of the analysed animals, whereas PCB 138 and 153 in the lungs. TEQs levels calculated for only dioxin-like PCBs were low: 0.32 and 0.29 pg WHO-PCB-TEQ·g^?1 fat in liver of red deer and roe deer, respectively. The mean PCB concentrations obtained in our study for organs of roe deer and red deer were several times lower than those reported elsewhere. These findings show that the investigated roe and red deer originated from an area with low levels of PCB contamination.     

Outdoor air particle-bound trace metals in four selected communities in Ibadan,Nigeria

Trace metal concentrations were determined in particulate matter (PM₁₀) in ambient air of four purposively selected residential areas in Ibadan, Nigeria namely Bodija market (BM), Ojo Park (OP), Oluyole Estate (OE) and University of Ibadan (UI). PM₁₀ was determined in the morning (7–10 a.m.) and afternoon (2–5 p.m.) for 12 weeks in the dry season months of January–March using a volumetric sampler following standard procedures and levels compared with WHO guideline limits. Glass-fibre filter papers exposed to the particulate matter were digested using appropriate acid mixtures, and the digest analysed for trace metals including Ni, Cr, Mn, Zn, and Pb using ICPMS method and levels compared with WHO limits. Data was analysed using ANOVA and Pearson correlation test at 5 % level of significance. The highest mean PM₁₀ concentrations 502.3 ± 39.9 μg/m³ were recorded in the afternoon period at BM, while the lowest concentration 220.6 ± 69.9 μg/m³ was observed in the morning hours at UI. There was a significant difference between the PM₁₀ levels across the various locations (p < 0.05), and all the levels were higher than WHO limit of 50 μg/m³. The highest levels of Ni, Zn and Pb were recorded at BM, which also had the highest PM₁₀ burden. The trend in Pb levels across the locations was BM > UI > OP > OE with the highest level 5.70 μg/m³ in BM nearly fourfolds WHO limits of 1.5 μg/m³. There was a significant correlation between PM₁₀ and Ni (p < 0.05).Urban communities with increased human activities especially motor traffic recorded both higher levels of PM₁₀ and toxic trace metals. There is need to carry out source apportionment to establish the origin of these trace metals in future studies.     

A compilation of field surveys on gaseous elemental mercury (GEM) from contrasting environmental settings in Europe,South America,South Africa and China: separating fads from facts

Mercury is transported globally in the atmosphere mostly in gaseous elemental form (GEM, \( {\text{Hg}}_{\text{gas}}^{0} \) ), but still few worldwide studies taking into account different and contrasted environmental settings are available in a single publication. This work presents and discusses data from Argentina, Bolivia, Bosnia and Herzegovina, Brazil, Chile, China, Croatia, Finland, Italy, Russia, South Africa, Spain, Slovenia and Venezuela. We classified the information in four groups: (1) mining districts where this contaminant poses or has posed a risk for human populations and/or ecosystems; (2) cities, where the concentration of atmospheric mercury could be higher than normal due to the burning of fossil fuels and industrial activities; (3) areas with natural emissions from volcanoes; and (4) pristine areas where no anthropogenic influence was apparent. All the surveys were performed using portable LUMEX RA-915 series atomic absorption spectrometers. The results for cities fall within a low GEM concentration range that rarely exceeds 30 ng m^?3, that is, 6.6 times lower than the restrictive ATSDR threshold (200 ng m^?3) for chronic exposure to this pollutant. We also observed this behavior in the former mercury mining districts, where few data were above 200 ng m^?3. We noted that high concentrations of GEM are localized phenomena that fade away in short distances. However, this does not imply that they do not pose a risk for those working in close proximity to the source. This is the case of the artisanal gold miners that heat the Au–Hg amalgam to vaporize mercury. In this respect, while GEM can be truly regarded as a hazard, because of possible physical–chemical transformations into other species, it is only under these localized conditions, implying exposure to high GEM concentrations, which it becomes a direct risk for humans.     

The pollution characteristics of PM<Subscript>2.5</Subscript> and correlation analysis with meteorological parameters in Xinxiang during the Shanghai Cooperation Organization Prime Ministers’ Meeting

The pollution characteristics of PM_2.5 and correlation analysis with meteorological parameters in Xinxiang during the Shanghai Cooperation Organization Prime Ministers’ Meeting were investigated. During the whole meeting, nine PM_2.5 samples were collected at a suburban site of Xinxiang, and the average concentration of PM_2.5 was 122.28 μg m^?3. NO₃ ^?, NH₄ ⁺, SO₄ ^2? accounted for 56.8% of the total water-soluble ions. In addition, with an exception of Cl^?, all of water-soluble ions decreased during the meeting. Total concentrations of crustal elements ranged from 6.53 to 185.86 μg m^?3, with an average concentration of 52.51 μg m^?3, which accounted for 82.5% of total elements. The concentrations of organic carbon and elemental carbon were 7.71 and 1.52 μg m^?3, respectively, lower than those before and after the meeting. It is indicated that during the meeting, limiting motor vehicles is to reduce exhaust emissions, delay heating is to reduce the fossil fuel combustion, and other measures are to reduce the concentration of PM_2.5. The directly dispersing by mixing layerheight increase and the indirectly reducing the formation of secondary aerosol by low relative humidity, andthese are the only two key removing mechanisms of PM_2.5 in Xinxiang during the meeting.