1. Introduction
Atmospheric dustfall is one of the main urban atmospheric particulate pollutants [
1,
2], and it has important environmental indication function [
3]. As an indirect carrier, atmospheric dustfall brings pollutants from the atmosphere to the land surface or water, seriously affecting aquatic and terrestrial ecosystem [
4]. With the continuous economic development and the urbanized advancement acceleration, the amounts of atmospheric dustfall and its carrying pollutants are increasing. As an important part of atmospheric particles, water-soluble inorganic ions (WSIIs) generally account for 20~60% of the mass concentration of particles [
5,
6], and even up to 80% [
7]. WSIIs such as sulphate, nitrate, and ammonium are hygroscopic [
6], which affect the visibility of atmosphere through the absorption and scattering of light [
8]. They can also affect the acidity and alkalinity of atmospheric precipitation [
9]. In addition, the atmospheric dustfall’s contribution rate to the accumulation of heavy metals in topsoil ranks first among various exogenous input factors [
10]. Heavy metal pollutants are not to be degraded and will cause long-term damage to human health and ecological environment [
11,
12]. Therefore, the study on the contamination features of WSIIs and heavy metals in the atmospheric dustfall and topsoil has become a research focus in environmental science field in recent years.
In 1975, Day et al. [
13] first proposed the new term “city street dust fall.” Since then, scholars have studied it in various aspects, including particle size characteristics [
14], temporal distribution [
15], spatial distribution [
16], and chemical composition [
17,
18]. At present, the researches on WSIIs in atmospheric particles mainly focus on the analysis of pollution characteristics [
6], source analysis [
7], transformation mechanism between gaseous pollutants and WSIIs [
19], and the effects on aerosol optical properties [
8]. The researches on heavy metals in atmospheric particulates mainly focus on the heavy metal content [
20], spatial distribution [
21], pollution characteristics, source identification, ecological risk, and health risk assessment [
22]. Currently, many studies on air particle pollution in China have paid close attention to the chemical composition, occurrence form, and source analysis. However, the research areas of both WSIIs and heavy metals in atmospheric particles are mostly concentrated in large and medium-sized cities or developed regions such as Beijing-Tianjin-Hebei region [
23,
24,
25] and Yangtze River Delta [
26]. There is very little research on atmospheric dustfall in arid and underdeveloped areas in the northwest China. Besides, analysis combining the data from heavy metals with WSIIs could provide interesting information, but there are few studies in this field.
Lanzhou is the capital of Gansu Province. It is located in the west of Loess Plateau and the Yellow River valley basin in the northeastern of Qinghai-Tibet Plateau, which is a typical “valley belt” city. The soil texture of Lanzhou is IV class self-weight collapsible loess, which is easy to produce dust pollution after human disturbance. The climate in this area is arid and the temperature inversion is serious in winter. The external input of sand dust from the surrounding deserts, a lot of smoke and dust emissions from industrial enterprises, exhausts from vehicles, and the continuous acceleration of construction results in a prominent PM contamination in Lanzhou City. Because of the special topography and climate, the atmospheric PM contamination pattern in Lanzhou may be different from those in other cities which are located in plain areas, for example, Beijing-Tianjin-Hebei region and Yangtze River Delta. Therefore, studying WSIIs and heavy metals in atmospheric dustfall and topsoil will be helpful to understand the regularities of their migration, transport, and diffusion in the atmospheric-soil system.
This article takes the main urban area of Lanzhou as the research area. The contents and correlation of WSIIs (Cl−, F−, NO2−, NO3−, SO42−, K+, Na+, Mg2+, and Ca2+) and heavy metals (Pb, Cu, Zn, Cr, Cd, and Ni) in dustfall and topsoil were studied. The sources of WSIIs and heavy metals in dustfall were distinguished. The potential ecological risks of heavy metals in dustfall and topsoil were evaluated, with an aim to supply a reference for the atmospheric particle pollution prevention and control in Lanzhou.
2. Materials and Methods
2.1. Study Area and Sample Collection
Lanzhou is located at the Yellow River Valley and surrounded by hills. In the south there are Gaolan mountain and other loess hills, with an altitude of 1700~2500 m, which are 180~1000 m higher than that of Lanzhou City; in the north there are Loess hills and low or middle mountains, with an altitude of about 1700 m, which are about 180 m higher than that of Lanzhou City. The landform of the main urban area of Lanzhou City is erosion accumulation valley plain. The geological structure of Lanzhou City belongs to the middle uplift zone of Qilian in Kunlun-Qinling geosyncline fold system. Because the Yellow River runs through Lanzhou City, local groundwater is relatively rich. The groundwater in Lanzhou City is mainly loose rock pore phreatic water. Landslides, collapses, and debris flows are the main types of geological disasters in Lanzhou City. The average annual temperature is 10.3 °C. The annual average sunshine hours are 2446, the frost-free period is 180 days, and the average annual precipitation is 327 mm, which mainly concentrate from June to September. It is an important industrial base and transportation hub in northwest China. The main urban areas of Lanzhou (Chengguan District, Anning District, Qilihe District, and Xigu District, excluding suburban counties) were selected as the research areas. The atmospheric dustfall and topsoil samples were obtained at each sample position. The sampling sites are shown in
Figure 1.
The samples were collected in July 2017, and there was no rainfall during the week before the collection. The atmospheric dustfall was sampled at a height of 1.0 to 2.0 m (being close to the height of human respiratory tract exposure) using hairbrush to collect the dust on clean paper and transfer it into self-sealing bag. Sampling was kept away from the demolition, factories, and other areas that could cause local pollution. Four samples were collected at each position by the three-point mixed method, which means that three samples are collected at each sample point and mixed as one atmospheric dustfall sample. A total of 40 samples were obtained. Topsoil samples (depth 2–10 cm) were collected on the bare ground or green belt near the sampling points of atmospheric dustfall by the three-point mixed method, and a total of ten samples were obtained. Both the atmospheric dustfall samples and the topsoil samples were pretreated as follows: the branches, leaves, etc., in the sample were removed. The samples were laid in a beaker and dried in an oven (DZF—6020A, Shanghai Lichen Instrument Technology Co., Ltd., Shanghai, China) at 105 °C for 3 h, and then the samples were crushed and passed through 20 mesh and 200 mesh sieves for reserve. The quartering method was applied for sample weighting.
2.2. Materials
The chemicals NaF, NaCl, KNO3, NaNO2, NaNO3, Na2SO4, Mg(NO3)2·6H2O, and Ca(NO3)2·4H2O with superior grade purity, standard reserve solutions (1000 mg·L−1) containing Cl−, F−, NO2−, NO3−, SO42−, Na+, K+, Mg2+, and Ca2+, high purity argon (purity ≥ 99.999%), standard reserve solutions of Cu, Zn, Cr, Cd, Ni, Pb (1000 mg·L−1), internal standard solutions of Rh (10 μg·mL−1), mass spectrometry tuning solution (Be, In, U, etc. 10 mg·L−1), and the reagents HNO3, HF, HCl, CH4N2S, and H2O2 with superior grade purity were bought from Baiyin Liangyou Chemical Reagents CO., LTD (Baiying, China). Soil for extractable trace elements (GBW07437, National Institute of Metrology, Beijing, China). Quality Control Materials (QCM-TW001 and QCM-CW001, Institute for Environmental Reference Materials of Ministry of Environmental Protection, Beijing, China). All standard solutions were prepared with ultrapure water (CSR-1-10, > 18.2 MΩ·cm, Beijing ASTK Technology Development Co., Ltd., Beijing, China).
2.3. Analytical Methods
For ion determination, 0.1 g of sample was weighed placed into a 500-mL centrifugal tube and 100 mL of ultrapure water was added. The tube cap was tightened, and ultrasonic extraction in water bath was conducted at 25 °C for 30 min. The tube was rotated at 4000 r·min−1 for 15 min. The supernatant was taken and filtered through a 0.22-μm membrane. All the samples were analyzed parallelly three runs with blank. Instead of weighing the sample, blank sample was prepared according to the same steps. WSIIs (Cl−, F−, NO2−, NO3−, SO42−, K+, Na+, Mg2+, and Ca2+) were determined by ion chromatograph (881 Compact IC pro, Metrohm, Herisau, Switzerland)). The detection limits of Cl−, F−, NO2−, NO3−, SO42−, K+, Na+, Mg2+, and Ca2+ were 0.002, 0.001, 0.004, 0.005, 0.004, 0.002, 0.001, 0.001, and 0.003 mg·L−1, respectively. The standard curve correlation coefficient was above 0.995. The relative quasi-deviation of the three measurements was less than 9% and the recovery rates ranged from 86.0% to 89.7%. The anion column was Metrosep A Supp 5-150 (Metrohm, Herisau, Switzerland). 3.2 mmol·L−1 Na2CO3 and 1 mmol·L−1 NaHCO3 were the eluent. The cationic column was Metrosep C4-150 (Metrohm, Herisau, Switzerland), and 5.6 mmol·L−1 HNO3 was the eluent.
As for heavy metal determination, a pretreatment was carried out for samples with an Automatic Digestion Instrument (Politech DigestLinc ST60D, Beijing, China). Total of 0.5 g of each sample was weighed and put into Teflon beaker, 10 mL of HNO3-HCl mixed solution (167.5 mL HCl and 55.5 mL HNO3 were added to 500 mL ultrapure water, with a constant volume up to 1 L) was added. The beaker was covered and heated for 2 h at 100 °C, then shaken well and cooled for 20 min, diluted to 50 mL with ultrapure water, stood for 2 h and measured after filtration. Inductively coupled plasma mass spectrometry (ICP-MS X series II, Thermo Fisher Scientific (China) Co., Ltd., Shanghai, China) was used to determine the contents of metal elements. Soil for extractable trace elements (GBW07437) were selected as solid reference materials to draw working curve, which could basically eliminate the matrix interference in the determination of heavy metals in environmental soil by ICP-MS. Quality control materials (QCM-TW001 and QCM-CW001) were selected as reference solution for ICP-MS analysis. The standard curve correlation coefficient was above 0.9980. The relative quasi-deviation of the three measurements was less than 10%. The recovery rates are higher than 90%.
2.4. Assessment Methods
Correlation analysis (CA) was used to characterize the variation rule of each element and the correlation degree among measured variables. The communality of each indicator was extracted by principal component analysis (PAC), then the compositional patterns were compared among the samples to find out the mutual influence factors. SPSS 22.0 software (IBM, New York, NY, USA) was used for PCA and CA.
Geo-accumulation index (
Igeo) is an index that reflects the effect of man-made activities and natural geological processes on heavy metal pollution [
27,
28], and it is described by the Equation (1).
where
Bi is the environmental background value in Gansu province [
29],
Ci refers to the measured value of the metal
i. 1.5 is a correction factor related to the geological and sedimentary characteristics of rocks. If
Igeo ≤ 0, it means the medium is uncontaminated; 0 <
Igeo < 1, from uncontaminated to moderately contaminated; 1 <
Igeo < 2, moderately contaminated; 2 <
Igeo < 3, from moderately to strongly contaminated; 3 <
Igeo < 4, strongly contaminated; 4 <
Igeo < 5, from strongly to extremely contaminated; and
Igeo > 5, extremely contaminated [
30].
The degree of the potential environmental risk of heavy metals could reflect by potential ecological risk index (
RI), which is a comprehensive index that regards environmental effect, ecological effect, and toxicity [
31].
where
Eri means the single factor potential ecological risk index.
Ci refers to the measured value of heavy metal
i in the sample.
C0 means heavy metal
i environmental background value in Gansu province [
29].
Tri is toxic response factor of a given element, which for Zn, Cr, Cu, Ni, Pb, and Cd are 1, 2, 5, 5, 5, and 30, respectively [
31]. On the basis of Hakanson’s research, the single factor potential ecological risk is usually regarded as safety while
Eri < 40, slight 40 ≤
Eri < 80, moderate 80 ≤
Eri < 160, considerable 160 ≤
Eri < 320, and high
Eri ≥ 320. The comprehensive potential ecological risk is usually regarded as low while
RI < 150, moderate 150 ≤
RI < 300, considerable 300 ≤
RI < 600, and high
RI ≥ 600 [
31].