3.2.1. Characteristics at the Annual Scale
The annual average PM
2.5 and PM
10 concentrations in the study area from 2015 to 2018 were statistically analysed, and the results are shown in
Figure 2. Overall, the PM
2.5 and PM
10 concentrations in the study area decreased each year from 2015 to 2018, with annual average PM
2.5 concentrations of 69.9, 62.2, 58.0 and 49.7 μg·m
−3, respectively. The annual mean PM
10 concentrations were 123.8, 110.6, 108.5 and 100.4 μg·m
−3, respectively. The concentration decreased by 23.5 μg·m
−3 over four years, with an average annual change of approximately 7.8 μg·m
−3. The overall PM
2.5/PM
10 ratio in the study area reached approximately 0.53, which indicated that PM
2.5 was the main component of PM
10 in the study area. Moreover, the PM
2.5/PM
10 ratio decreased each year from 2015 to 2018, with values of 0.56, 0.56, 0.53 and 0.49, respectively, indicating that while the overall PM concentration decreased, and the proportion of PM
2.5 to PM
10 therefore decreased.
The spatial distribution of the annual mean particle concentration was obtained with the spatial interpolation method, and the results are shown in
Figure 3. Overall, the trend of PM concentration in the study area was high in the southeast and low in the northwest. The overall concentrations in Chengde, Zhangjiakou and other cities in the north were low, while those in Beijing, Tianjin and other central cities were slightly higher. Relatively high values were mostly concentrated in Xingtai, Hengshui, Handan, Shijiazhuang, Baoding and other cities in the south.
In 2015, the highest annual average PM2.5 concentration reached Level 6 and was mainly distributed in southern cities of the BTH region, accounting for 14.7% of the total area. Nearly half of the experimental region had concentrations exceeding the Level 2 limit, and regions with Level 4, 3 and 2 concentrations accounted for 20.7%, 30.2% and 1.1%, respectively, of the total area. Compared to 2015, the annual average concentration decreased significantly in 2016; the areas with Grade 5 and 6 concentrations in the south shrank rapidly. In addition, areas with annual average concentrations exceeding the Grade 2 limit decreased to 31.9%, while the areas with Grade 4, 3 and 2 concentrations sequentially expanded towards the south, accounting for 30.0%, 26.0% and 12.1%, respectively, of the total area. In 2017, the Level 5 concentration range contracted slightly, with an annual average concentration of 23.5% in the area, exceeding the Level 2 limit, and the areas of Level 4, 3 and 2 concentrations continued to expand southwards, accounting for 32.0%, 26.2% and 18.3%, respectively, of the area. In 2018, the annual average concentration declined considerably, and the areas of Grade 4, 3 and 2 concentrations continued to expand from north to south, with the corresponding areas accounting for 41.8%, 33.6% and 24.4%, respectively, of the total area. However, most of these areas exhibited excellent and good air quality conditions.
In 2015, the highest annual average PM10 concentration reached Level 5, which exceeded the secondary limit of the national standard and was concentrated in the south, accounting for 24.0% of the total area. The lowest level was Level 3, which was largely distributed in the northern part of the study area, accounting for 33.1% of the area. The remaining areas, accounting for 42.9% of the total area, had Level 4 concentrations. In 2016, the Level 5 concentration range contracted, and the Level 2 limit was exceeded in only 6.7% of the whole region. The Level 3 range expanded towards the south, accounting for 43.6% of the total area. The remaining areas, accounting for 49.7% of the total area, all had Level 3 concentrations. In 2017, the areas at each concentration level remained the same as those in 2016, among which the Level 5 concentration range slightly expanded, with Shijiazhuang–Baoding and Handan–Xingtai forming two Level 5 concentration centres, while Level 3 still dominated in the north. In 2018, the concentration declined greatly, Level 5 areas disappeared, and the annual average concentration in the whole region reached below the Level 2 limit. Among the various cities, the southern cities and the northern part of Tangshan, accounting for 44.2% of the total area, mostly had Level 4 concentrations, while the remaining areas reached Level 3 concentrations and accounted for 55.8% of the total area.
It is generally acknowledged that PM
2.5 and PM
10 are produced by a combination of natural and human activities. Of these components, PM
2.5 originates from industrial waste gas, automobile exhaust, fuel combustion and secondary PM formed through a series of reactions, while PM
10 originates from natural dust and dust generated by traffic and urban construction [
18,
19,
20,
21]. The higher the PM
2.5/PM
10 ratio is (which may be attributed to automobile exhaust and straw burning), the higher the mass concentration of fine particles in the air, and the more serious the fine particulate pollution and threat to human health. The lower the PM
2.5/PM
10 ratio is (which may be caused by natural factors such as dust and sandstorms), the higher the mass concentration of inhalable particles in the air [
22,
23,
24,
25].
Figure 4 shows the spatial distribution of the annual mean value of the PM
2.5/PM
10 ratio. The highest value of the PM
2.5/PM
10 ratio each year was centred in Beijing, followed by Tianjin, Baoding, Langfang and other areas south of Beijing, while the ratio in the mountainous areas and grasslands in the north was lower. The spatial distribution of the ratio displayed a positive relationship with the degree of economic development and intensity of human activities. The road density and traffic volume in Beijing are both large. Motor vehicle exhaust emissions constitute an important source of PM in the atmosphere, which more notably contributes to PM
2.5. Human activities in the northern mountains and grasslands are limited, and the proportion of natural emissions of PM sources is high. Especially in seasons with a low vegetation coverage, the proportion of dust, particularly dust particles with larger diameters, in PM sources increases, resulting in a relatively low PM
2.5/PM
10 ratio. In 2015, the ratio in downtown Beijing reached Level 8, the ratio in Tianjin, Langfang, Baoding and other cities mostly reached Level 7, the ratio in other areas mostly reached Level 6, and the ratio in some northern areas reached Level 5. In 2016, a high value exceeding Level 9 was observed at the centre of Beijing, and the range of areas with Level 8 values expanded south. In 2017, the ratio decreased, and the range of areas with values above Level 7 contracted sharply, while those at Levels 8 and 9 nearly disappeared. In 2018, the ratio further decreased, with only Level 7 values observed in downtown Beijing, Tianjin and Hengshui and Level 3 occurring in the north.
The analysis above indicated that from 2015 to 2018, the PM2.5 and PM10 concentrations and the PM2.5/PM10 ratio all exhibited a declining trend, and the regions with relatively high values contracted or even disappeared, which demonstrated the achievements of emission reduction efforts across the study area. This achievement was closely related to policies and measures such as industrial transformation and upgrading, energy structure reform, strict control of mobile source emissions, and forestland area expansion.
3.2.2. Characteristics at the Seasonal Scale
Statistics of the average seasonal PM
2.5 and PM
10 concentrations in the study area from 2015 to 2018 were calculated. The results are shown in
Figure 5. Overall, there were already stated seasonal differences between the PM
2.5 and PM
10 concentrations in the study area. The average PM
2.5 concentrations in winter, spring, summer and autumn reached 87.8, 55.6, 43.1 and 55.3 μg·m
−3, respectively. The average concentrations in winter were approximately twice as high as those in summer, and the average concentrations in spring and autumn were similar to those in winter and summer. The maximum concentration was 106.5 μg·m
−3 in the winter of 2017, and the minimum concentration was 34.6 μg·m
−3 in the summer of 2018. Hence, the maximum value was approximately 3.1 times the minimum value. The average PM
10 concentrations in the four seasons were 139.6, 125.6, 78.9 and 101.5 μg·m
−3, respectively. Generally, the concentration in winter was 1.8 times that in summer. The maximum value was 160.0 μg·m
−3 in the winter of 2017, and the minimum value reached 67.0 μg·m
−3 in the summer of 2018. Thus, the maximum concentration was approximately 2.4 times the minimum concentration. Heating activities in the winter greatly increase the combustion of coal and other energy sources. Moreover, the surface inversion layer often occurs in winter, acting as a lid to block the upward vertical turbulence of air, which prevents the diffusion of particles and retains it in the atmosphere for a longer time [
26,
27]. In addition, due to the withering of vegetation, the particle adsorption and blocking ability of the vegetation is greatly reduced, and the particle concentration is therefore highest in the winter [
13]. In summer, the temperature rises, air convection is strong, and the horizontal and vertical transport capacities of the atmosphere are notable, which enhances its particle dilution and diffusion capacities. Furthermore, the lush vegetation during the growing period strongly affects particle sedimentation. In addition, increases in precipitation play a notable role in scouring and inhibiting particles, thus the particle concentration in summer is generally low [
28,
29]. Meteorological conditions such as temperature, humidity, precipitation and wind speed, and natural conditions such as vegetation cover in spring and autumn vary from those in winter and summer. In addition, frequent dust weather conditions and large-scale straw burning are the main sources of PM in spring and autumn, respectively. The PM
2.5/PM
10 ratio also exhibits an obvious seasonal regularity, with the average values in the four seasons reaching 0.63, 0.44, 0.55 and 0.54, respectively. The PM
2.5/PM
10 ratio is the highest in winter, lowest in spring and moderate in summer and autumn. This is mainly attributable to the dry air and scarce precipitation in spring, which results in a dry and unconsolidated surface. Furthermore, the vegetation coverage is relatively low, and the high average wind speed is attributed to stronger winds. These conditions jointly promote the easy entry of surface dust into the atmosphere [
12,
23,
30]. However, PM
10 have a larger diameter, and the contribution rate of dust to PM
10 is higher than that to PM
2.5, which is one of the reasons for the relatively low PM
2.5/PM
10 ratio in spring [
31]. In winter, the temperature is low, people in the study area start to use heating sources more, and coal-based energy consumption increases [
32,
33,
34]. Moreover, incomplete motor vehicle fuel combustion occurs due to the low temperature and air pressure, all of which contribute to higher PM
2.5 levels, resulting in an increased PM
2.5/PM
10 ratio in winter [
12,
34].
The spatial distribution of the seasonal mean PM concentration was determined with the spatial interpolation method, and the results are shown in
Figure 6. In winter, the average seasonal PM
2.5 concentration was the highest among the four seasons, with the highest value reaching Level 8, which is moderate pollution. Shijiazhuang–Baoding and Xingtai–Handan formed two centres, accounting for 5.5% of the total area. The concentration gradually decreased from these high-value centres to the surrounding areas, of which the southern areas mostly had concentrations of Level 5 and above, and areas with Level 5, 6 and 7 ratios reached 16.2%, 16.6% and 21.0%, respectively. In addition, 59.3% of the area experienced light or moderate pollution. Most of the concentrations in the north reached Levels 3 and 4, accounting for 22.6% and 18.1%, respectively, of the total area. The concentration in spring was notably lower than that in winter, and the whole area did not meet the pollution standard. In the south, Level 4 concentrations were observed, accounting for 61.4% of the total area. Most of the concentrations in the north reached Levels 2 and 3, accounting for 5.6% and 33.1%, respectively, of the total area. In summer, the concentration was the lowest of the year, and in the south, the concentrations mostly reached Levels 3 and 4, with areas of 67.2% and 6.1%, respectively. The range of areas with Level 2 concentrations expanded southward, accounting for 26.7% of the total area, and their air quality was excellent. The concentration in autumn slightly increased, approaching the average regional concentration in spring, but there were differences in its spatial distribution: the concentration in the south was slightly higher than that in spring, and the concentration in the north was slightly lower than that in spring. Moreover, Level 5 concentrations were observed in the south, accounting for 5.7% of the area, and the areas with Level 2, 3 and 4 concentrations reached 15.6%, 28.6% and 50.1%, respectively.
The average seasonal PM10 concentration was also highest in winter, and the ranges of areas with Level 5 and 6 concentrations, accounting for 21.0% and 17.4%, respectively, of the regional area, were concentrated in the southern region, which was mildly polluted. Areas with Level 3 and 4 concentrations occupied most of the north, accounting for 32.1% and 29.4%, respectively, of the regional area. In the spring, the relatively high-value area in the south contracted, and the change in the PM10 concentration distribution in the north exhibited a different trend from that of the PM2.5 concentration distribution. The concentration increased slightly, but the relatively low-value area contracted northwards, which was related to the frequent dusty weather conditions in spring. Level 5 concentrations were observed in southern cities, accounting for 7.8% of the total area. The range of areas with Level 4 concentrations was reduced to 10.8%, while the rest of the area exhibited Level 3 concentrations, accounting for 81.4% of the regional area. In summer, the concentration was the lowest and the concentration in the whole region remained below Level 4. Except for areas with Level 4 concentrations, which accounted for 6.4% of southern cities such as Xingtai and Handan, the remaining area (93.6%) exhibited Level 3 conditions. In autumn, the concentration rose slightly. Except for the Level 5 concentrations in Shijiazhuang, which accounted for 0.3% of the area, all other areas failed to meet the pollution standard, with the ranges of areas with Level 3 and 4 concentrations accounting for 55.4% and 44.4%, respectively, of the total area.
Figure 7 shows the spatial distribution of the seasonal mean value of the PM
2.5/PM
10 ratio. The PM
2.5/PM
10 ratio varied greatly between different seasons. In winter, the ratio was the highest, with a Level 9 value observed at the centre of Beijing, Level 8 values occurring in the surrounding areas and Level 7 values distributed in the other areas. PM
2.5 was the main component of PM
10. The spring ratio was the lowest of the whole year, with Level 6 values observed in Beijing, Tianjin, Langfang and Cangzhou, Level 4 values only occurring in certain areas of Zhangjiakou and Chengde in the north, and Level 5 values distributed in the other areas. In summer, two Level 7 centres were formed in Beijing and Tianjin, whereas most of the other regions reached Level 6. In autumn, the ratio in Beijing increased, exhibiting Level 8 and 9 values, while the range of areas with Level 7 values slightly expanded, and other areas exhibited similar levels to those in summer.
The analysis above indicated that the PM2.5 and PM10 concentrations and PM2.5/PM10 ratio in the study area exhibited significant seasonal regularity. In the different seasons, meteorological conditions such as temperature, humidity, precipitation, wind speed and air pressure were quite different and imposed varying influences on the processes of particle generation, emission, diffusion and transmission. Moreover, vegetation growth exhibited obvious seasonal regularity, and PM inhibition or promotion differed between the various seasons. The types and intensities of human activities were also closely related to season, especially in the study area in North China, where heating in winter requires a large amount of energy from sources such as coal, which notably impacts the PM concentration and is one of the main reasons for the frequent occurrence of winter smog in the study area in recent years.
3.2.3. Characteristics at the Monthly Scale
Statistics of the monthly mean values of the PM
2.5 and PM
10 concentrations in the study area from 2015 to 2018 were computed. The results are shown in
Figure 8. In general, the PM
2.5 and PM
10 concentrations in the study area exhibited obvious periodicity with the annual cycle. Generally, peak and valley values occurred each year. Every year, the peak PM
2.5 concentration mostly occurred in December and January, when the average monthly concentration reached 96.1 and 90.7 μg·m
−3, respectively. The valley value mostly occurred in August and September, when the average monthly concentration reached 37.2 and 39.7 μg·m
−3, respectively. The highest value was 135.7 μg·m
−3 in December 2015, and the lowest value was 27.9 μg·m
−3 in September 2018. Hence, the highest value was 4.9 times the lowest value. The monthly mean PM
2.5 concentration demonstrated a decreasing trend from January to June. After a slight increase in July, the concentration reached its lowest value in August and then increased from August to December. The main reason for the slight increase in concentration in July could be that higher temperatures and increased precipitation promote the occurrence of photochemical reactions and, thus, facilitate the formation of secondary particles. Each year, the peak PM
10 concentration mostly occurred in December, January and March, and the average monthly concentration reached 152.9, 143.1 and 137.6 μg·m
−3, respectively. The valley values mostly occurred in August and September, and the average monthly concentrations reached 69.3 and 78.4 μg·m
−3, respectively. The highest value was 199.3 μg·m
−3 in December 2015, and the lowest value was 57.6 μg·m
−3 in August 2018. Hence, the highest concentration was 3.5 times the lowest concentration. After the average monthly PM
10 concentration decreased from January to February, it rose slightly in March and exhibited a gradual downwards trend from March to August. After reaching the lowest value in August, the concentration increased from August to December. The main reason that the concentration in March was slightly higher than that in February could include the melting of snow and ice due to the rising temperature in spring, and since most vegetation had not yet entered the growing season, this led to surface dust exposure to air, which easily generated dusty weather under windy conditions and promoted the entry of larger-sized particles into the atmosphere. The PM
2.5/PM
10 ratio also revealed a periodic trend, which usually formed double peaks and double valleys in a given year: the PM
2.5 and PM
10 levels were high in December or January of the following year, and the first peak value was formed due to the increase in PM
2.5 concentration facilitated by coal combustion and the ground inversion layer phenomenon. Frequent dusty weather in spring gradually enhanced the ratio, and the first valley value was reached in May. Subsequently, the rapid increase in temperature and humidity promoted the chemical transformation of secondary organic aerosols and accelerated the PM
2.5 formation process. In addition, because the scouring effect of precipitation on PM
10 was greater than that on PM
2.5, the ratio reached its second peak value in July. A decrease in precipitation, temperature, humidity and wind speed caused a slight reduction in the ratio after July and formed the second valley in September. Subsequently, with the rapid drop in temperature and arrival of the heating period, the amount of burning of coal and other energy sources rapidly increased, a large amount of PM
2.5 was discharged into the air, and the ratio reached a peak value again.
The spatial distribution of the monthly mean particle concentration was calculated with the spatial interpolation method, and the results are shown in
Figure 9. The monthly mean PM
2.5 concentration exhibited a large spatial difference, where the concentration in the northern region was low and constant, and most of the concentrations reached Levels 2, 3 and 4 throughout the year. There was a large fluctuation in the south, with Level 9 concentrations were observed in December when the concentration was the highest and Level 3 concentrations observed in August when the concentration was the lowest. In January, 58.6% of the whole area was slightly or moderately polluted, and high values were concentrated in the south, of which areas with Level 7 and 8 concentrations accounted for 15.5% and 16.0%, respectively, of the total area. From February to April, the high-concentration range contracted rapidly, areas with Level 7 and 8 concentrations disappeared in February, those with Level 6 concentrations disappeared in March, those with Level 5 and above concentrations all disappeared after April, and the concentration across the whole region declined to match the national secondary standard. From May to August, the concentration dropped further, and by August, areas with Level 4 concentrations completely disappeared and the range of areas with excellent air quality reached 41.8%, the highest of the whole year. From September to November, the concentration began to rise rapidly, and in September, Level 4 concentrations reappeared. In November, Level 5 and 6 concentrations reoccurred in the southern region, covering 53.5% of the total area. In December, the concentration was the highest of the whole year. The Shijiazhuang–Baoding and Xingtai–Handan areas contained two heavily polluted areas with concentrations reaching Level 9, accounting for 8.1% of the total area. Areas with concentrations at Levels 7 and 8 accounted for 27.7% of the total area, and those with concentrations at Levels 5 and 6 accounted for 26.4% of the total area. Of the whole region, 62.1% of the area was lightly, moderately or heavily polluted, which was the highest pollution level of the whole year.
Compared to PM2.5, the spatial difference and temporal fluctuation in the monthly mean PM10 concentration were relatively limited. In January, the ranges of areas with Level 3–6 concentrations gradually transitioned from north to south, and 38.9% of the southern area exhibited light pollution levels. In February, the concentration decreased, and Level 6 concentrations disappeared. In March, the monthly concentration increased, especially in the northern region, with the Level 4 concentration range expanding greatly from south to north, while a Level 5 concentration was observed in Tangshan. From April to August, the concentration dropped rapidly. In May, Level 5 concentrations disappeared, and the concentration across the whole region declined below the national Level 2 standard. In August, Level 4 concentrations disappeared, and the whole region had Level 3 concentrations. In September, Level 4 concentrations were observed again and remained through the rest of the year. From October to December, the concentration increased rapidly. In November, Level 5 concentrations reoccurred, and in December, Level 6 concentrations were observed again. In Shijiazhuang and Handan, even Level 7 concentrations were reached. The moderately polluted area accounted for 0.5% of the total area, and 48.1% of the whole area was slightly or moderately polluted.
The spatial centre of gravity was calculated for the average monthly PM
2.5 and PM
10 concentrations each month, and the migration trajectory of the centre of gravity in each month was determined. The results are shown in
Figure 10. The results indicated that the average monthly centre of gravity of the PM
2.5 and PM
10 concentrations in the BTH region was concentrated along the borders of Langfang, Cangzhou and Baoding, and the migration trajectory exhibited a certain regularity. Generally, the migration trend of the centre of gravity throughout the year demonstrated that the centre moved rapidly from southwest to northeast and then gradually moved back to the southwest from the northeast. In January, the centre of gravity was located in the southwest. From February to March, the centre of gravity moved sharply to the northeast, remained in the northeast from March to June, moved slightly towards the west in July, remained west of Central China from August to November, moved sharply towards the southwest in December, and returned to the southwest in January of the following year. In winter (December, January, and February), the centre of gravity was located in the southwest, which indicated that although the overall concentration in the area in winter increased, the southwestern part of the study area had a concentrated, high pollution level. In spring (March, April, and May), the centre of gravity was located in the northeast, which indicated that there was a greater decrease in concentration in high-value areas in the south from winter to spring than in the north, which may be related to the frequent occurrence of dusty weather conditions in the north. In summer (June, July, and August) and autumn (September, October and November), the centre of gravity remained at the centre of the region, which indicated that the degree of concentration change at each location across the region remained relatively stable and that the overall change was similar.
3.2.4. Characteristics at the Hourly Scale
Hourly mean values of the PM
2.5 and PM
10 concentrations in the study area from 2015 to 2018 were calculated for each season, and the results are shown in
Figure 11. The average PM concentration scale indicated a diurnal cycle, mostly revealing a trend of double peaks and double valleys. At night, the temperature was relatively low, the boundary layer height decreased, and the atmospheric turbulence activity weakened, which did not facilitate PM diffusion. Hence, the PM concentration was higher at night or in the early morning, and the first peak was reached. Human activities greatly decreased at night, as most of the population was sleeping, and the PM concentration gradually dropped at night, reaching the first valley in the early morning. With the sun rising in the morning, the temperature gradually increased, human activities increased, and the speed of secondary particle generation increased. Moreover, during the morning rush hour period, motor vehicles discharged a large amount of tail gas into the atmosphere and dislodged road dust, and the particle concentration reached its second peak in the morning [
27]. Subsequently, with the increasing boundary layer height, the atmospheric turbulence activity was enhanced, and these conditions facilitated PM diffusion. Furthermore, after the morning peak, the traffic volume on the roads decreased slightly, so the PM concentration was reduced to a certain extent and declined further until it reached the second valley in the afternoon. In the evening, as the sun went down, the temperature rapidly dropped, and with the traffic peak at night and the sharp increase in kitchen oil smoke emissions at dinner time, PM continuously accumulated in the atmosphere and the concentration rose again and reached a peak value in the evening or early morning [
28,
29,
35].
The timing of peak and valley PM concentrations during the four seasons and their corresponding concentrations are listed in
Table 3. The peak value at night mostly occurred from 22:00 to 0:00 the next day, the valley during the morning mostly occurred from 4:00 to 7:00, the peak value in the morning mostly occurred from 8:00 to 10:00, and the valley in the afternoon mostly occurred from 15:00 to 17:00. Usually, the morning peak occurred between ~7:00 and 9:00 and the evening peak occurred between 17:00 and 19:00. The morning and evening peaks imposed a certain delayed effect on the PM concentration variation [
13,
36,
37,
38]. Comparing the two peaks and valleys during the same season, the results indicated that during each season, the valley in the afternoon was obviously lower than that in the morning, which was the lowest value throughout the whole day. This finding verified that the favourable meteorological conditions for PM diffusion in the afternoon obviously affected the PM concentration reduction. There were seasonal differences between the heights of the two peaks. The night peak in autumn and winter was higher than the morning peak, but the opposite was true in spring and summer. The atmosphere in autumn and winter was more stable than that in summer, and relatively calm weather occurred, which resulted in PM sedimentation and diffusion taking more time than in summer. Moreover, the temperature in winter was low and the night lasted longer. The heating demand at night greatly increased the amount of burning of coal and other energy sources, resulting in the highest concentration at night. Comparing the occurrence times of the peaks and valleys among the four seasons, we observed that the peaks in the morning occurred the earliest in summer and the latest in winter, while the occurrence times of the valleys in the afternoons were the opposite, which was directly related to sunrise, sunset and sunshine duration. The morning temperature rise occurred later than in summer, and the afternoon temperature drop occurred earlier. In addition, the PM
2.5 concentration at night in summer remained relatively stable, increasing slowly from 17:00 to 8:00 the next day, with no obvious night peak or early morning valley. A single peak and a single valley were observed throughout the whole day, which may be related to factors such as higher summer temperatures, longer sunshine durations, shorter night periods, and more persistent human activities. In addition, in summer, construction and earth excavation activities occurred in more cities at night, and popular evening dining activities could also promote higher concentrations on summer nights [
39].
The PM
2.5/PM
10 ratio exhibited a single peak and a single valley in winter and spring, and the ratio slowly decreased during the day after reaching the full-day peak in the morning. The PM
2.5/PM
10 ratio then gradually increased after reaching a valley in the evening. In summer and autumn, a pattern with double peaks and double valleys was observed, which differed from that in winter and spring in that the ratio increased from approximately 9:00 to 15:00, which may be attributed to the relatively high temperature and humidity during the day in summer and autumn, thus intensifying the occurrence of secondary reactions and increasing the PM
2.5 concentration. The surface temperature is generally low at night, and inversion occurs when the surface temperature is lower than the air temperature. Consequently, stable atmospheric conditions limit vertical airflow, which is conducive to the dry settlement of coarse particles and accumulation of fine particles, resulting in a gradual increase in the night-time ratio. With increasing human activity intensity during the day, rough road dust becomes resuspended in the air. In addition, a large amount of construction dust greatly influences the PM
10 concentration, which gradually reduces the PM
2.5/PM
10 ratio. In summer and autumn, the afternoon valley occurred slightly later than in winter and spring, which was caused by the slightly later inversion occurrence time in summer and autumn than in winter and spring [
30,
40,
41].