内蒙古科尔沁沙地临界起沙阈值的范围确定

临界起沙阈值可表征地表土壤的可蚀性,是风蚀起沙研究中非常重要的物理量之一。基于微气象学方法,将沙尘浓度和垂直沙尘通量均开始增加且至少持续0.5 h所对应的摩擦速度(或风速)确定为临界起沙摩擦速度u_*t(或临界起沙风速U_t)。利用内蒙古科尔沁沙地地区2010-2013年春季大气环境综合观测资料,分析了不同沙尘天气过程(扬沙、沙尘暴和强沙尘暴)起沙阶段沙尘浓度和垂直沙尘通量随摩擦速度的演变特征,精细确定了该地区临界起沙摩擦速度(u_*t)和临界起沙风速(U_t)的范围分别为0.45±0.20和6.5±3.0 m/s,同时讨论了不同起沙判据对确定临界起沙阈值产生的影响。相比而言,采用的起沙判据尽可能地排除了沙尘输送和沉降过程的影响,适用于不同的沙尘天气类型,使沙尘粒子进入大气的起沙结果更趋于合理,其结果可为建立统一、合理的起沙判据提供参考。     

Quantitative detection of mass concentration of sand-dust storms via wind-profiling radar and analysis of <Emphasis Type="Italic">Z</Emphasis>-<Emphasis Type="Italic">M</Emphasis> relationship

With the aim to achieve quantitative monitoring of sand-dust storms in real time, wind-profiling radar is applied to monitor and study the process of four sand-dust storms in the Tazhong area of the Taklimakan Desert. Through evaluation and analysis of the spatial-temporal distribution of reflectivity factor, it is found that reflectivity factor ranges from 2 to 18 dBz under sand-dust storm weather. Using echo power spectrum of radar vertical beams, sand-dust particle spectrum and sand-dust mass concentration at the altitude of 600 ～ 1500 m are retrieved. This study shows that sand-dust mass concentration reaches 700?μg/m³ under blowing sand weather, 2000?μg/m³ under sand-dust storm weather, and 400?μg/m³ under floating dust weather. The following equations are established to represent the relationship between the reflectivity factor and sand-dust mass concentration: Z?=?20713.5?M ^0.995 under floating dust weather, Z?=?22988.3?M ^1.006 under blowing sand weather, and Z?=?24584.2?M ^1.013 under sand-dust storm weather. The retrieval results from this paper are almost consistent with previous monitoring results achieved by former researchers; thus, it is implied that wind-profiling radar can be used as a new reference device to quantitatively monitor sand-dust storms.     

Mass concentration of PM10 and PM2.5 fine-dispersed aerosol fractions in the Eastern Gobi Desert

Results are presented of monitoring measurements of the mass concentration of PM₁₀ (particles with the size of less than 10 μm) and PM_2.5 (less than 2.5 μm) fine-dispersed aerosol fractions at the Sainshand and Zamyn-Üüd stations located in the Gobi Desert of Mongolia. Revealed are the annual variations of the mass concentration of PM₁₀ and PM_2.5 fine-dispersed aerosol fractions at these stations in 2008. The maximum values of monthly mean concentration during the year were observed in May in the period of dust storms. On the days with the steady calm weather, the mass concentrations of PM₁₀ and PM_2.5 varied within 5–8 μg/m³ (PM₁₀) and 3–5 μg/m³ (PM_2.5) at the Sainshand station. During the dust storms, the maximum values of concentration exceeded 1400 μg/m³ (PM₁₀) and 380 μg/m³ (PM_2.5) that is by 28 (PM₁₀) and 15 (PM_2.5) times higher than the maximum permissible concentration for the European Union. Results are given of studying the frequency and duration of dust storms in recent 20 years (1991–2010) in the Eastern Gobi Desert.     

Seasonal and annual trends of carbonaceous species of PM<Subscript>10</Subscript> over a megacity Delhi,India during 2010–2017

PM₁₀ samples were collected to characterize the seasonal and annual trends of carbonaceous content in PM₁₀ at an urban site of megacity Delhi, India from January 2010 to December 2017. Organic carbon (OC) and elemental carbon (EC) concentrations were quantified by thermal-optical transmission (TOT) method of PM₁₀ samples collected at Delhi. The average concentrations of PM₁₀, OC, EC and TCA (total carbonaceous aerosol) were 222?±?87 (range: 48.2–583.8 μg m^?3), 25.6?±?14.0 (range: 4.2–82.5 μg m^?3), 8.7?±?5.8 (range: 0.8–35.6 μg m^?3) and 54.7?±?30.6 μg m^?3 (range: 8.4–175.2 μg m^?3), respectively during entire sampling period. The average secondary organic carbon (SOC) concentration ranged from 2.5–9.1 μg m^?3 in PM₁₀, accounting from 14 to 28% of total OC mass concentration of PM₁₀. Significant seasonal variations were recorded in concentrations of PM₁₀, OC, EC and TCA with maxima during winter and minima during monsoon seasons. In the present study, the positive linear trend between OC and EC were recorded during winter (R²?=?0.53), summer (R²?=?0.59) and monsoon (R²?=?0.78) seasons. This behaviour suggests the contribution of similar sources and common atmospheric processes in both the fractions. OC/EC weight ratio suggested that vehicular emissions, fossil fuel combustion and biomass burning could be the major sources of carbonaceous aerosols of PM₁₀ at the megacity Delhi, India. Trajectory analysis indicates that the air mass approches to the sampling site is mainly from Indo Gangetic plain (IGP) region (Uttar Pradesh, Haryana and Punjab etc.), Thar desert, Afghanistan, Pakistan and surrounding areas.     

Size distributions and dry deposition fluxes of water-soluble inorganic nitrogen in atmospheric aerosols in Xiamen Bay,China

Size-segregated aerosol particles were collected using a high volume MOUDI sampler at a coastal urban site in Xiamen Bay, China, from March 2018 to June 2020 to examine the seasonal characteristics of aerosol and water-soluble inorganic ions (WSIIs) and the dry deposition of nitrogen species. During the study period, the annual average concentrations of PM₁, PM_2.5, PM₁₀, and TSP were 14.8?±?5.6, 21.1?±?9.0, 35.4?±?14.2 μg m^?3, and 45.2?±?21.3 μg m^?3, respectively. The seasonal variations of aerosol concentrations were impacted by the monsoon with the lowest value in summer and the higher values in other seasons. For WSIIs, the annual average concentrations were 6.3?±?3.3, 2.1?±?1.2, 3.3?±?1.5, and 1.6?±?0.8 μg m^?3 in PM₁, PM_1-2.5, PM_2.5–10, and PM_>10, respectively. In addition, pronounced seasonal variations of WSIIs in PM₁ and PM_1-2.5 were observed, with the highest concentration in spring-winter and the lowest in summer. The size distribution showed that SO₄^2?, NH₄⁺ and K⁺ were consistently present in the submicron particles while Ca²⁺, Mg²⁺, Na⁺ and Cl^? mainly accumulated in the size range of 2.5–10 μm, reflecting their different dominant sources. In spring, fall and winter, a bimodal distribution of NO₃^? was observed with one peak at 2.5–10 μm and another peak at 0.44–1 μm. In summer, however, the fine mode peak disappeared, likely due to the unfavorable conditions for the formation of NH₄NO₃. For NH₄⁺ and SO₄^2?, their dominant peak at 0.25–0.44 μm in summer and fall shifted to 0.44–1 μm in spring and winter. Although the concentration of NO₃–N was lower than NH₄–N, the dry deposition flux of NO₃–N (35.77?±?24.49 μmol N m^?2 d^?1) was much higher than that of NH₄–N (10.95?±?11.89 μmol N m^?2 d^?1), mainly due to the larger deposition velocities of NO₃–N. The contribution of sea-salt particles to the total particulate inorganic N deposition was estimated to be 23.9—52.8%. Dry deposition of particulate inorganic N accounted for 0.95% of other terrestrial N influxes. The annual total N deposition can create a new productivity of 3.55 mgC m^?2 d^?1, accounting for 1.3–4.7% of the primary productivity in Xiamen Bay. In light of these results, atmospheric N deposition could have a significant influence on biogeochemistry cycle of nutrients with respect to projected increase of anthropogenic emissions from mobile sources in coastal region.

     

武汉市道路扬尘源排放清单及空间分布特征研究

参考AP-42方法的采样规范（USEPA,2011）,对武汉市13个城区的不同类型道路采集了137个扬尘样,并记录采样面积、车流情况、车道状况、地理位置、周围环境以及气象数据要素信息,得到了不同类型道路的积尘负荷,估算了其扬尘排放因子和排放量.结果表明：武汉总城区尘负荷由大到小顺序为支路 > 次干道 > 主干道 > 快速路,其中支路平均尘负荷为2.396 g/m²,快速路为0.852 g/m²,远城区平均尘负荷是主城区平均尘负荷的2倍左右.各类型道路不同粒径范围的道路交通扬尘排放因子大小顺序为支路 > 次干路 > 主干路 > 高速路,与尘负荷大小趋势一致.2016年道路交通扬尘源TSP的年排放量为156 931.4 t,PM₁₀的年排放量为39 868.7 t,PM_2.5的年排放量为11 574.8 t,其不确定性范围分别为-24.7%~31.4%、-31.3%~32.9%、-31.8%~30.5%.其中主干道扬尘排放量最大,其TSP、PM₁₀和PM_2.5的年排放量分别为64 447.1、16 372.9和4 753.4 t.     

PM10 Observed at a Meteorological Station in Beijing: Historical Trend and Implications

Inhalable particles(PM₁₀), with aerodynamic equivalent diameters that are generally 10 micrometers or smaller, are basic pollutants in many areas, especially in northern China, and thus the pollution from PM₁₀inhalable particulate matter is a growing concern for public health. Independent long-term observations are necessary to evaluate the efficacy of PM₁₀reduction actions. Variations in the PM₁₀concentration from 2006 to 2017 at an observation statio...     

Assessment of PM<Subscript>2.5</Subscript> chemical compositions in Delhi: primary vs secondary emissions and contribution to light extinction coefficient and visibility degradation

Haze-fog conditions over northern India are associated with visibility degradation and severe attenuation of solar radiation by airborne particles with various chemical compositions. PM_2.5 samples have been collected in Delhi, India from December 2011 to November 2012 and analyzed for carbonaceous and inorganic species. PM₁₀ measurements were made simultaneously such that PM_10–2.5 could be estimated by difference. This study analyzes the temporal variation of PM_2.5 and carbonaceous particles (CP), focusing on identification of the primary and secondary aerosol emissions, estimations of light extinction coefficient (b_ext) and the contributions by the major PM_2.5 chemical components. The annual mean concentrations of PM_2.5, organic carbon (OC), elemental carbon (EC) and PM_10–2.5 were found to be 153.6 ± 59.8, 33.5 ± 15.9, 6.9 ± 3.9 and 91.1 ± 99.9 μg m^?3, respectively. Total CP, secondary organic aerosols and major anions (e.g., SO₄ ^2? and NO₃ ^?) maximize during the post-monsoon and winter due to fossil fuel combustion and biomass burning. PM_10–2.5 is more abundant during the pre-monsoon and post-monsoon. The OC/EC varies from 2.45 to 9.26 (mean of 5.18 ± 1.47), indicating the influence of multiple combustion sources. The b_ext exhibits highest values (910 ± 280 and 1221 ± 371 Mm^?1) in post-monsoon and winter and lowest in monsoon (363 ± 110 and 457 ± 133 Mm^?1) as estimated via the original and revised IMPROVE algorithms, respectively. Organic matter (OM =1.6 × OC) accounts for ~39 % and ~48 % of the b_ext, followed by (NH₄)₂SO₄ (~21 % and ~24 %) and EC (~13 % and ~10 %), according to the original and revised algorithms, respectively. The b_ext estimates via the two IMPROVE versions are highly correlated (R² = 0.95, root mean square error = 38 % and mean bias error = 28 %) and are strongly related to visibility impairment (r = ?0.72), mostly associated with anthropogenic rather than natural PM contributions. Therefore, reduction of CP and precursor gas emissions represents an urgent opportunity for air quality improvement across Delhi.     

Ionic and elemental composition of PM<Subscript>2.5</Subscript> aerosols over the Caribbean Sea in the Tropical Atlantic

To characterize atmospheric particulate matter equal or less than 2.5 μm in diameter (PM_2.5) over the Tropical Atlantic Ocean, aerosol sampling was carried out in Puerto Rico during August and September, 2006. Aerosols were analyzed by ion chromatography for water-soluble inorganic and organic ions (including Na⁺, NH₄ ⁺, Mg²⁺, Ca²⁺, K⁺, Cl^?, SO₄ ^2?, NH₄ ⁺, F^?, methanesulfonate (MSA), and oxalate), by inductive coupled plasma mass spectrometry (ICPMS) for trace elements (Al, Fe, Zn, Mn, Cu, Ni, V, Pb, Cr, Sb, Co, Sc, Cd), and by scanning electron microscopy for individual aerosol particle composition and morphology. The results show that the dominant cations in aerosols were Na⁺, (mean: 631 ng m^?3), accounting for 63.8 % of the total cation and NH₄ ⁺ (mean: 164 ng m^?3), accounting for 13.8 % of the total cation measured in this study. The main inorganic anions were Cl^? (576 ng m^?3, 54.1 %) and SO₄ ^2? (596 ng m^?3, 38.0 %). The main organic anion was oxalate (18 ng m^?3). Crustal enrichment factor calculations identified 62 % of the trace elements measured (Cu, Ni, V, Co, Al, Mn, Fe, Sc, and Cr) with crustal origin. Single particle analysis demonstrated that 40 % of the aerosol particles examined were Cl^? rich particles as sodium chloride from seawater and 34 % of the total particles were Si-rich particles, mainly in the form of aluminosilicates from dust material. Based on the combination of air-mass trajectories, cluster analysis and principal component analysis, the major sources of these PM_2.5 particles include marine, Saharan dust and biomass burning from West Africa; however, volcanic emissions from the Soufriere Hills in Montserrat had significant impact on aerosol composition in this region at the time of sample collection.     

Carbonaceous and inorganic species in PM<Subscript>10</Subscript> during wintertime over Giridih,Jharkhand (India)

Ambient concentrations of organic carbon (OC), elemental carbon (EC) and water soluble inorganic ionic components (WSIC) of PM₁₀ were studied at Giridih, Jharkhand, a sub-urban site near the Indo Gangatic Plain (IGP) of India during two consecutive winter seasons (November 2011–February 2012 and November 2012–February 2013). The abundance of carbonaceous and water soluble inorganic species of PM₁₀ was recorded at the study site of Giridih. During winter 2011–12, the average concentrations of PM₁₀, OC, EC and WSIC were 180.2?±?46.4; 37.2?±?6.2; 15.2?±?5.4 and 18.0?±?5.1 μg m^?3, respectively. Similar concentrations of PM₁₀, OC, EC and WSIC were also recorded during winter 2012–13. In the present case, a positive linear trend is observed between OC and EC at sampling site of Giridih indicates the coal burning, as well as dispersed coal powder and vehicular emissions may be the source of carbonaceous aerosols. The principal components analysis (PCA) also identifies the contribution of coal burning? +?soil dust, vehicular emissions?+?biomass burning and seconday aerosol to PM₁₀ mass concentration at the study site. Backward trajectoy and potential source contributing function (PSCF) analysis indicated that the aerosols being transported to Giridih from upwind IGP (Punjab, Haryana, Uttar Pradesh and Bihar) and surrounding region.     

Particulate morphology and elemental characteristics: variability at middle Indo-Gangetic Plain

Airborne particulates were monitored at an urban location of middle Indo-Gangetic Plain (IGP) and subsequently analyzed for particulate diversity and mixing states. Exceptionally high particulate loadings were found both in case of coarser (PM₁₀: 157.5 ± 102.9 μgm^?3, n = 46) and finer particulates (PM_2.5: 92.5 ± 49.8 μgm^?3). Based on particulate morphology and elemental composition, five different clusters of particulates namely tarball, soot, sulphur-rich, aluminosilicate and mineral species were found to dominate. Soot particles (0.1–5 μm) were found to be partly coated, having voids filled by coating material without being completely engulfed. A specific type of amorphous, carbonaceous spherules was evident in wintertime fine particulates signifying emissions from biomass burning and wild fire. Traces of S, Na and Ca were found associated with carbonaceous agglomerates suggesting its metal scavenging behavior. Particle laden filters were further processed for metallic and water soluble ionic species to constitute aerosol composition. Coarser particulates were characterized with higher metallic species (9.2–17.8 %), mostly of crustal origin (Ca: 5.5 %; Fe: 1.6 %; Zn: 1.3 % and Na: 3.8 %) while PM_2.5 also revealed their association with metallic components (6.0–14.9 %) having Ca (4.6 %), Fe (0.9 %) and K (0.8 %) as principle constituents. Ca, Na and NH₄ ⁺ found to generate chloride and sulphate salts thus affecting particulate hygroscopicity. Elevated fractions of NO₃ ^? and K⁺ in PM_2.5 signified contribution of biomass burning while presence of Cl^? with carbonaceous aerosols having traces of Si and K denoted contribution of farming and burning practices. Black carbon aerosol exhibited significant seasonal variability (6.9?21.9 μgm^?3) which support larger association of carbonaceous aerosols in particle micrograph.     

2010年民勤沙地近地面沙尘气溶胶浓度特征

为了更好地研究沙尘气溶胶起沙和输送特征,2010年4—5月,在民勤周边沙地利用EZ LIDAR ALS300&ALS450型激光雷达和 GRIMM 180型颗粒物采样器进行了大气气溶胶的外场连续观测,取得了晴天、浮尘、扬沙和沙尘暴天气条件下沙尘气溶胶总后向散射垂直剖面图和PM₁₀、PM_2.5、PM_1.0质量浓度采样资料,其中包含“0424”特强沙尘暴过程资料。结果表明：春季民勤近地层大气中沙尘气溶胶浓度较高,且随气象要素的变化很大;在整个观测期内,PM₁₀、PM_2.5、PM_1.0的平均质量浓度分别为202.3、57.4 μg/m³、16.7 μg/m³。在不同天气条件下,PM₁₀、PM_2.5、PM_1.0质量浓度的变化有很好的相关性,但变化趋势有所不同。在沙尘暴天气条件下,PM₁₀的日平均质量浓度高达2469.1μg/m³,是背景天气条件下PM10日平均质量浓度的100多倍,是浮尘天气条件下PM10日平均质量浓度的8倍,是扬沙天气条件下PM₁₀日平均质量浓度的2倍。PM_2.5在沙尘暴天气下日平均质量浓度为460.3 μg/m³,是背景天气条件下PM_2.5日平均质量浓度的45倍,是浮尘天气条件下PM_2.5日平均质量浓度的6倍,是扬沙天气条件下PM_2.5日平均质量浓度的1.4倍。PM_1.0在沙尘暴天气条件下的日平均浓度为92.7 μg/m³,是背景天气条件下PM_1.0日平均浓度的13倍,是浮尘天气条件下PM_1.0日平均浓度的7倍,是扬沙天气条件下PM_1.0日平均浓度的1.3倍。可见,风速增大时沙尘粒子浓度的增加对粒子粒径是有选择的,小粒子比重随沙尘浓度增加而相对减小,大粒子比重随沙尘浓度增加而相对增多;通过对“0424”特强沙尘暴过程的研究表明,一次沙尘暴过程往往包括沙尘暴、扬沙和浮尘天气中的两种类型;通过对激光雷达数据分析发现,在强沙尘暴发生过程当中,民勤沙地发生了非常严重的风蚀起沙现象。     

Atmospheric ionic species in PM2.5 and PM1 aerosols in the ambient air of eastern central India

This study elucidates the characteristics of ambient PM_2.5 (fine) and PM₁ (submicron) samples collected between July 2009 and June 2010 in Raipur, India, in terms of water soluble ions, i.e. Na⁺, NH ₄ ⁺ , K⁺, Mg²⁺, Ca²⁺, Cl^?, NO ₃ ^? and SO ₄ ^2? . The total number of PM_2.5 and PM₁ samples collected with eight stage cascade impactor was 120. Annual mean concentrations of PM_2.5 and PM₁ were 150.9?±?78.6 μg/m³ and 72.5?±?39.0 μg/m³, respectively. The higher particulate matter (PM) mass concentrations during the winter season are essentially due to the increase of biomass burning and temperature inversion. Out of above 8 ions, the most abundant ions were SO ₄ ^2? , NO ₃ ^? and NH ₄ ⁺ for both PM_2.5 and PM₁ aerosols; their average concentrations were 7.86?±?5.86 μg/m³, 3.12?±?2.63 μg/m³ and 1.94?±?1.28 μg/m³ for PM_2.5, and 5.61?±?3.79 μg/m³, 1.81?±?1.21 μg/m³ and 1.26?±?0.88 μg/m³ for PM₁, respectively. The major secondary species SO ₄ ^2? , NO ₃ ^? and NH ₄ ⁺ accounted for 5.81%, 1.88% and 1.40% of the total mass of PM_2.5 and 11.10%, 2.68%, and 2.48% of the total mass of PM₁, respectively. The source identification was conducted for the ionic species in PM_2.5 and PM₁ aerosols. The results are discussed by the way of correlations and principal component analysis. Spearman correlation indicated that Cl^? and K⁺ in PM_2.5 and PM₁ can be originated from similar type of sources. Principal component analysis reveals that there are two major sources (anthropogenic and natural such as soil derived particles) for PM_2.5 and PM₁ fractions.     

Characteristics of Elemental Composition of PM2.5 in the Spring Period at Tongyu in the Semi-arid Region of Northeast China

Continuous observations of mass concentration and elemental composition of aerosol particles （PM2.5） were conducted at Tongyu, a semi-arid site in Northeast China in the spring of 2006. The average mass concentration of PM2.5 at Tongyu station was 260.9±274.4 μg m^-3 during the observation period. Nine dust events were monitored with a mean concentration of 528.0±302.7 μgm^-3. The PM2.5 level during non- dust storm （NDS） period was 111.65±63.37 μg m^-3. High mass concentration shows that fine-size particles pollution was very serious in the semi-arid area in Northeast China. The enrichment factor values for crust elements during the dust storm （DS） period are close to those in the NDS period, while the enrichment factor values for pollution elements during the NDS period are much higher than those in the DS period, showing these elements were from anthropogenic sources. The ratios of dust elements to Fe were relative constant during the DS period. The Ca/Fe ratio in dust aerosols at Tongyu is remarkably different from that observed in other source regions and downwind regions. Meteorological analysis shows that dust events at Tongyu are usually associated with dry, low pressure and high wind speed weather conditions. Air mass back-trajectory analysis identified three kinds of general pathways were associated with the aerosol particle transport to Tongyu, and the northwest direction pathway was the main transport route.     

Atmospheric abundance of HULIS during wintertime in Indo-Gangetic Plain: impact of biomass burning emissions

This study reports for the first-time the ambient concentrations of HULIS mass (HULIS-OM, Humic-like substances) and HULIS-C (carbon) in PM₁₀ (particulate matter with aerodynamic diameter?≤?10 μm) from the Indo-Gangetic Plain (IGP at Kanpur, wintertime). HULIS extraction followed by purification and isolation protocol with methanol: acetonitrile (1:1 v/v) on HLB (Hydrophilic-Lipophilic Balanced) cartridge has been established. Quantification of HULIS-C was achieved on a total organic carbon (TOC) analyser whereas HULIS-OM was determined gravimetrically. Consistently high recovery (> 90%) of HULIS-C based on analysis of Humic standard (sodium salt of Humic acid) suggested suitability of our established analytical protocol involving solvent extraction, purification and accurate quantification of HULIS. HULIS-OM varied from 17.3–38 μg m^?3 during daytime and from 19.8–40.6 μg m^?3 during night in this study. During daytime the HULIS-OM constituted 20–30% mass fraction of OM_Total and 10–15% of PM₁₀ mass. However, a relatively low contribution of HULIS-OM has been observed during the night. This observation has been attributed to higher concentrations of OM and PM₁₀ in night owing to nighttime chemical reactivity and condensation of organics in conjunction with shallower planetary boundary layer height. Strong correlation of HULIS-C with K⁺_BB (R²?>?0.80) and significant day-night variability of HULIS-C/WSOC ratio in conjunction with air-mass back trajectories (showing transport of pollutants from upwind IGP) suggest biomass burning emission and secondary transformations as important sources of HULIS over IGP. High-loading of atmospheric PM₁₀ (as high as 440 μg m^?3) with significant contribution of water-soluble organic aerosols (WSOC/OC: ~ 0.40–0.80) during wintertime highlights their plausible potential role in fog and haze formation and their impact on regional-scale atmospheric radiative forcing over the IGP.     

Observation of wind shear during evening transition and an estimation of submicron aerosol concentrations in Beijing using a Doppler wind lidar

The wind speed and direction measured over six months by a Doppler wind lidar (Windcube-8) were compared with wind cup anemometers mounted on the 325-m Beijing meteorological tower (BMT). Five mountain–plain wind cases characterized by wind direction shear were selected based on the high-frequency (1.1 s) wind profile of the Windcube-8 and analyzed with 1-h mesoscale surface weather charts. Also analyzed was the relationship between in-situ PM₁ (aerodynamic diameter ≤ 1 μm) concentrations measured at 260 m on BMT and the carrier-to-noise ratio (CNR) of the co-located Windcube-8. The results showed that the 10-min averaged wind speed and direction were highly correlated (R = 0.96–0.99) at three matched levels (80, 140, and 200 m). The evening transition duration was 1–3 h, with an average wind speed of 1 m s^–1 at 80 m above the ground. In addition, there was a zero horizontal-wind-speed zone along the wind direction shear line, and in one case, the wind speed was characterized by a Kelvin–Helmholtz gravity wave. The variability of the PM₁ concentrations was captured by the CNR of the Windcube-8 in a fair weather period without the long-range transport of dust.     

The aerosol radiative effect on a severe haze episode in the Yangtze River Delta

Due to increased aerosol emissions and unfavorable weather conditions, severe haze events have occurred frequently in China in the last 10 years. In addition, the interaction between the boundary layer and the aerosol radiative effect may be another important factor in haze formation. To better understand the effect of this interaction, the aerosol radiative effect on a severe haze episode that took place in December 2013 was investigated by using two WRF-Chem model simulations with different aerosol configurations. The results showed that the maximal reduction of regional average surface shortwave radiation, latent heat, and sensible heat during this event were 88, 12, and 37 W m^–2, respectively. The planetary boundary layer height, daytime temperature, and wind speed dropped by 276 m, 1°C, and 0.33 m s^–1, respectively. The ventilation coefficient dropped by 8%–24% for in the central and northwestern Yangtze River Delta (YRD). The upper level of the atmosphere was warmed and the lower level was cooled, which stabilized the stratification. In a word, the dispersion ability of the atmosphere was weakened due to the aerosol radiative feedback. Additional results showed that the PM_2.5 concentration in the central and northwestern YRD increased by 6–18 μg m^–3, which is less than 15% of the average PM_2.5 concentration during the severely polluted period in this area. The vertical profile showed that the PM_2.5 and PM₁₀ concentrations increased below 950 hPa, with a maximum increase of 7 and 8 μg m^–3, respectively. Concentrations reduced between 950 and 800 hPa, however, with a maximum reduction of 3.5 and 4.5 μg m^–3, respectively. Generally, the aerosol radiative effect aggravated the level of pollution, but the effect was limited, and this haze event was mainly caused by the stagnant meteorological conditions. The interaction between the boundary layer and the aerosol radiative effect may have been less important than the large-scale static weather conditions for the formation of this haze episode.     

沙尘预报客观检验中最优实况资料和圆插值半径选择研究

使用2012～2014年每年3～5月CUACE（China Meteorological Administration Unified Atmospheric Chemistry Environment）模式地面沙尘浓度格点预报产品,预报员预报等级产品、实况地面观测沙尘等级和特征站观测PM10（空气动力学当量直径小于等于10 μm的颗粒物,即可吸入颗粒物）资料,并针对CUACE模式格点产品,选取不同半径对格点产品进行圆插值,从而对2012～2014年共25次沙尘过程值,采取3年总样本计算TS（Threat Score）评分,对格点产品适合的圆插值半径和预报产品适合的检验实况资料进行研究,结论如下:（1）如实况采用沙尘等级,模式插值半径与TS评分在浮尘或扬沙等级成近似线性下降关系,而在沙尘暴以上等级TS评分与插值半径关系几乎不大,最优插值半径可选为最小插值半径0.5°（经度/纬度）;如实况采用PM10资料,TS评分在浮尘或扬沙等级根据半径不同变化较为剧烈,沙尘暴以上等级TS评分与插值半径关系不大,可以采用浮尘或扬沙平均线3.5°为平均最优插值半径。如果沙尘过程较弱,插值半径可适当减小,以1°最合适;（2）对CUACE模式预报产品,沙尘等级观测TS评分可用性要优于PM10资料,但两者在沙尘暴以上等级评分差别不大,总体上CUACE模式最优检验实况资料可选为沙尘等级观测资料。对预报员沙尘预报产品,观测沙尘等级TS评分要远高于PM10,预报员沙尘预报产品最优检验实况资料为观测沙尘等级资料。     

The Parameterisation of Scalar Transfer over Rough Ice

We test a surface renewal model that is widely used over snow and ice surfaces to calculate the scalar roughness length (z _s ), one of the key parameters in the bulk aerodynamic method. For the first time, the model is tested against observations that cover a wide range of aerodynamic roughness lengths (z ₀). During the experiments, performed in the ablation areas of the Greenland ice sheet and the Vatnajökull ice cap in Iceland, the surface varied from smooth snow to very rough hummocky ice. Over relatively smooth snow and ice with z ₀ below a threshold value of approximately 10^?3 m, the model performs well and in accord with earlier studies. However, with growing hummock size, z ₀ increases well above the threshold and the bulk aerodynamic flux becomes significantly smaller than the eddy-correlation flux (e.g. for z ₀ = 0.01 m, the bulk aerodynamic flux is about 50% smaller). Apparently, the model severely underpredicts z _s over hummocky ice. We argue that the surface renewal model does not account for the deep inhomogeneous roughness sublayer (RSL) that is generated by the hummocks. As a consequence, the homogeneous substrate ice grain cover becomes more efficiently ‘ventilated’. Calculations with an alternative model that includes the RSL and was adapted for use over hummocky ice, qualitatively confirms our observations. We suggest that, whenever exceedance of the threshold occurs (z ₀  >  10^?3 m, i.e., an ice surface covered with at least 0.3-m high hummocks), the following relation should be used to calculate scalar roughness lengths, ln (z _s /z ₀)  =  1.5  ? 0.2 ln (Re _*)  ? 0.11(ln (Re _*))².     

塔克拉玛干沙漠腹地贴地层风沙流结构研究

利用微梯度集沙仪在塔克拉玛干沙漠腹地塔中地区实测的2014年7—8月贴地层输沙量梯度观测资料(观测高度区间0~5 mm、5~15 mm、15~35 mm、35~85 mm),对沙尘天气过程贴地层风沙流结构进行了研究。结果表明:(1)沙尘天气(沙尘暴和扬沙)过程中,随着风速的增大,各高度层输沙量也随之增大。沙尘暴天气中,风速7.5 m·s~(-1)时,15~35 mm处的百分含量超过5~15 mm处的百分含量,风速7.5 m·s~(-1)时,15~35 mm处的百分含量达到最大,其余各高度含量变化不明显。扬沙天气中,风速8.0 m·s~(-1)时,百分含量最大值出现在35~85 mm高度处,占48.9%,风速8.0 m·s~(-1)时,大小依次为:15~35 mm(49.5%)35~85 mm(31.7%)0~5 mm(12.7%)5~15 mm(9.2%)。(2)两种天气过程中,沙粒的平均粒径在垂直高度上均呈现先减小后增大的趋势。粒径峰值均处在125~250 um,极细砂含量最高,细砂次之。与扬沙天气相比,沙尘暴天气过程中极细砂、细砂、中砂在各高度层上的含量略微下降,粉尘含量有所升高。