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Kinetics and Mechanism of Atmospheric Photonucleation of Chlorinated Aromatic Compounds: o-Dichlorobenzene 氯代芳香族化合物-邻二氯苯的大气光核动力学和机理
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700521
S. N. Dubtsov, A. S. Khlynova, L. V. Kuibida, G. G. Dultseva

Aerosol particles which are generated in the atmosphere during photooxidation of organic compounds have reactive functional groups on their surfaces, which can be responsible for biological action of the organic aerosols. This work studies the kinetics and mechanism of atmospheric photonucleation of o-dichlorobenzene, which is a model of chlorinated aromatic hydrocarbons known for their environmental resistance, and the effects of water vapor and hydrogen peroxide on the yield and composition of aerosol products. The concentrations and sizes of aerosol particles were measured using a diffusion spectrometer of aerosol; the composition of gas and aerosol products of photonucleation was determined by high-performance liquid chromatography and gas chromatography-mass spectrometry. The formation mechanisms of identified products were determined based on the rate constants of elementary chemical reactions. It is shown that atmospheric photonucleation of dichlorobenzene does not result in photochemical generation of ozone in the surface air layer; quite contrary, dichlorobenzene photolysis products promote ozone destruction. The contribution of emissions of chlorinated aromatics into generation of organic aerosol in urban air is qualitatively estimated. The presence of reactive functional groups in the aerosol products enables us to assume negative biological action of the aerosol. The results can be used to model photochemical processes in polluted urban air.

大气中有机化合物光氧化过程中产生的气溶胶颗粒在其表面具有活性官能团,这些官能团可能负责有机气溶胶的生物作用。本文研究了邻二氯苯的大气光核动力学和机理,以及水蒸气和过氧化氢对气溶胶产物产率和组成的影响。邻二氯苯是一种以其环境抗性而闻名的氯代芳香烃模型。用气溶胶扩散光谱仪测量了气溶胶颗粒的浓度和大小;采用高效液相色谱和气相色谱-质谱联用技术测定了光核气体和气溶胶产物的组成。根据元素化学反应的速率常数确定了鉴定产物的形成机理。结果表明,大气中二氯苯的光核作用不会导致大气表层臭氧的光化学生成;相反,二氯苯光解产物促进臭氧破坏。对城市空气中氯代芳烃排放对有机气溶胶生成的贡献进行了定性估计。气溶胶产品中活性官能团的存在使我们能够假设气溶胶的负生物作用。研究结果可用于模拟受污染城市空气中的光化学过程。
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引用次数: 0
Aerosol Distribution over the Troposphere According to DELICAT Project Data 基于deliat项目数据的对流层气溶胶分布
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700570
A. E. Mamontov, O. V. Fedorova, M. E. Gorbunov

The analysis of statistical properties of aerosol density fluctuations at civil aviation flight altitudes can serve a starting point for the study of the random component of wind velocity field. This work analyzes fluctuations of the power of a scattered signal measured by an airborne lidar in the DELICAT (DEmonstration of LIdar based Clear Air Turbulence detection) project experiment. A new technique for the study of aerosol clouds based on 2D Fourier transform is introduced. Flight segments with constant aircraft altitude, direction, and speed were selected for the analysis. A signal was considered in the coordinate system where the distance from the aircraft to a scattering volume is plotted along the abscissa and aircraft path relative to an air mass is plotted along the ordinate. In these coordinates, aerosol clouds appear as stripes inclined at an angle of 45°. Spatial spectra of aerosol density fluctuations are derived. 2D spectra have a peak in the vicinity of the main diagonal of the frequency plane for regions with aerosol; their diagonal cross sections are equal to estimates of 1D spatial spectra of aerosol concentration fluctuations within the following approximations: (1) clouds are motionless on a time scale of about 1 min, (2) variations in the sounding line direction are negligible. The slope of 1D spectra was estimated. The results can serve as a basis for studying the random component of wind velocity fields.

分析民航飞行高度气溶胶密度波动的统计特性,可以作为研究风速场随机分量的一个起点。本文分析了在deliat(基于激光雷达的晴空湍流探测演示)项目实验中机载激光雷达测量的散射信号的功率波动。介绍了一种基于二维傅里叶变换的气溶胶云研究新技术。选取飞机高度、方向和速度不变的飞行段进行分析。在坐标系中考虑一个信号,其中飞机到散射体的距离沿横坐标绘制,飞机相对于气团的路径沿纵坐标绘制。在这些坐标中,气溶胶云以45°角倾斜的条纹呈现。导出了气溶胶密度波动的空间谱。在有气溶胶的地区,二维光谱在频率平面主对角线附近有一个峰;它们的对角线截面等于在下列近似范围内对气溶胶浓度波动的一维空间光谱的估计:(1)云在大约1分钟的时间尺度上是不动的;(2)探测线方向的变化可以忽略不计。估计了一维光谱的斜率。研究结果可作为研究风速场随机分量的基础。
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引用次数: 0
Time Behavior of Nitric Acid and its Influence on Polar Stratospheric Cloud Formation and Ozone Destruction in the Winter-Spring Stratosphere of the Arctic Based on Aura MLS Observations 基于Aura MLS观测的北极冬春季平流层硝酸时间行为及其对极地平流层云形成和臭氧破坏的影响
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700569
O. E. Bazhenov

The onsets of polar stratospheric cloud (PSC) formation and chlorine activation are so far considered to be the temperature threshold of formation of nitric acid trihydrate TNAT, below which the HNO3 concentration sharply increases in PSC particles. In this paper, the data on the temperature, ozone mixing ratio, and nitric acid (HNO3) mixing ratio in the Arctic stratosphere from the Aura MLS observations are used to calculate the minimal temperature, maximal negative deviations of ozone concentration from multiyear average, and maximal nitric acid (HNO3) mixing ratios and total columns at four Arctic sites: Eureka, Canada (EUR); Ny-Ålesund, Norway (NAD); Thule, Greenland (THU); and Resolute, Canada (RES). The maximal HNO3 concentrations decrease throughout the winter until late February at all observation sites under study due to condensation of gas-phase HNO3 on PSC particles. The mixing ratios start to grow after return of sunlight to polar latitudes due to PSC sublimation and HNO3 export from peripheral areas of the vortex during its deformation. The years, chosen for analysis (2010/2011, 2019/2020, 2020/2021, 2021/2022), cardinally differed in the stratospheric dynamics and in the state of ozone layer during winter and spring in the Arctic. Our results can be helpful for understanding the time dynamics of the HNO3 mixing ratio in the winter-spring stratosphere of the Arctic and its role in the chemical ozone destruction.

目前认为,极地平流层云(PSC)形成和氯活化的起始点是三水合硝酸TNAT形成的温度阈值,低于该温度,PSC颗粒中的HNO3浓度急剧升高。摘要数据温度、臭氧混合比,和硝酸(硝酸)混合比在北极平流层的光环MLS观测是用来计算最小温度,最大负偏差的臭氧浓度多年平均和最大硝酸(硝酸)混合比率和总列四个北极地点:尤里卡,加拿大(欧元);Ny-Ålesund,挪威(NAD);格陵兰岛图勒(THU);加拿大Resolute (RES)。在整个冬季至2月下旬,所有观测点的最大HNO3浓度都呈下降趋势,这是由于气相HNO3在PSC颗粒上凝结所致。在涡旋变形过程中,由于PSC升华和HNO3从涡旋外围区域输出,当阳光返回到极纬地区后,混合比开始增加。选择用于分析的年份(2010/2011年、2019/2020年、2020/2021年、2021/2022年)在北极冬季和春季的平流层动力学和臭氧层状态方面存在基本差异。研究结果有助于了解北极冬春季平流层HNO3混合比的时间动态及其在化学臭氧破坏中的作用。
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引用次数: 0
On a Possibility of Forming Soot (Black Carbon) by Strong Volcanic Eruptions 论强火山喷发形成烟尘(黑碳)的可能性
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S102485602670051X
S. A. Beresnev, E. D. Ganieva, M. S. Vasileva, L. B. Kochneva

Soot aerosol particles (black carbon) significantly contribute to atmospheric warming since they effectively absorb radiation in a wide wavelength range; along with greenhouse gases, they play an important role in the climate change. This work makes a critical analysis of the hypothesis of volcanogenic soot in the stratosphere (a possibility of producing black carbon nanoparticles by Plinian volcanic eruptions and their casting to high altitudes). Features of thermal decomposition of methane and origination of reduced carbon in a two-phase gas-ash volcanic column are discussed. Known data on the detection of carbonaceous particles in the atmosphere, their properties, and possible but not yet confirmed connection with strong volcanic eruptions are reviewed. The discovery of different reduced carbon forms in ashes of modern volcanic eruptions in Kamchatka (the phenomenon of volcanic carbon paragenesis) is commented on. Energy competition between two ways of formation of reduced carbon in the forms of soot nanoparticles and carbon products strongly mechanically bonded to pyroclastic material is discussed. The results can be useful in atmospheric aerosol physics and climatology for analyzing main sources of black carbon in the atmosphere.

烟尘气溶胶粒子(黑碳)由于能有效吸收宽波长范围内的辐射,对大气变暖有显著贡献;与温室气体一样,它们在气候变化中起着重要作用。这项工作对平流层中火山生成烟尘的假设进行了批判性分析(普林尼火山喷发产生黑碳纳米颗粒的可能性及其向高海拔地区的投射)。讨论了两相气灰火山柱中甲烷的热分解特征和还原碳的成因。对大气中碳质颗粒的已知探测数据、它们的性质以及可能但尚未证实的与强烈火山爆发的联系进行了回顾。评述了在堪察加半岛现代火山喷发灰烬中发现的不同的还原碳形态(火山碳共生现象)。讨论了以烟尘纳米颗粒和与火山碎屑材料强机械结合的碳产物形式形成的两种还原性碳之间的能量竞争。研究结果可用于大气气溶胶物理和气候学,分析大气中黑碳的主要来源。
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引用次数: 0
Formation and Consequences of Winter Temperature Inversions in the Atmosphere of Krasnoyarsk 克拉斯诺亚尔斯克冬季大气温度逆温的形成和后果
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700612
N. Ya. Shaparev, A. V. Tokarev, O. E. Yakubailik

The problem of atmospheric air pollution by fine particulate matter (PM2.5) in large industrial centers during winter is one of the most acute environmental threats affecting the life expectancy and quality of population. The study examines the processes of temperature inversion layer formation and its impact on atmospheric PM2.5 in Krasnoyarsk during the winter months of 2022–2024 based on data from a monitoring network, which measures air temperature, atmospheric pressure, wind speed and direction, PM2.5 concentration, and cloud cover, and data from an MTP-5 profiler, which determines the vertical distribution of atmospheric temperature. The multi-hour and multi-day regimes of radiation and advective inversions are analyzed. The necessary and sufficient conditions for their occurrence are established. The statistical dependences of PM2.5 concentration on the category and intensity of inversions are derived. The results can be used in short-term forecasting of temperature inversions and the associated periods of high PM2.5 air pollution in the city of Krasnoyarsk.

冬季大型工业中心的大气细颗粒物(PM2.5)污染问题是影响人口预期寿命和素质的最严重的环境威胁之一。本研究基于监测网络的气温、大气压、风速和风向、PM2.5浓度和云量的数据,以及MTP-5型大气温度垂直分布的数据,研究了2022-2024年冬季克拉斯诺亚尔斯克逆温层形成过程及其对大气PM2.5的影响。分析了辐射和平流逆温的多小时和数天状态。建立了它们发生的充分必要条件。推导了PM2.5浓度对逆温类型和强度的统计依赖性。研究结果可用于克拉斯诺亚尔斯克市气温逆温及相关PM2.5高污染期的短期预报。
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引用次数: 0
Experimental Characterization of Pulsed Laser Imaging with Frame-Based CCD Acquisition in Clear and Turbid Water 基于帧阵CCD采集的清混浊水中脉冲激光成像实验表征
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S102485602670065X
F. Almabouada

This work presents a short-range experimental characterization of underwater pulsed laser imaging using a free-running CCD camera operating in frame-based acquisition mode under controlled laboratory conditions. Unlike time-gated imaging systems, the proposed approach relies on asynchronous acquisition and post-processing-based frame selection and is intended for preliminary experimental study rather than direct alternative to gated imaging. The system performance is estimated in terms of signal-to-noise ratio (SNR), analytical contrast-to-noise ratio (CNR), and image-based contrast-to-noise ratio (IB-CNR). Experiments were conducted in a 1.2 m water tank, which limits light propagation range, under varying turbidity conditions and target properties. Results indicate that imaging performance strongly depends on water attenuation and object characteristics such as reflectivity and surface texture. In the configuration under study, turbid water can be associated with apparent changes in relative contrast for reflective targets, which reduces fine spatial detail visibility in low-reflectivity textured objects; in contrast, clear water better preserves high-frequency information. The study confirms the relevance of frame-based CCD acquisition for exploratory underwater imaging analysis and emphasizes that comparisons with time-gated systems are primarily model-based rather than experimentally validated and should not be interpreted as physically equivalent.

这项工作提出了水下脉冲激光成像的近距离实验特性,使用自由运行的CCD相机在受控的实验室条件下以帧为基础的采集模式工作。与时间门控成像系统不同,该方法依赖于异步采集和基于后处理的帧选择,旨在进行初步实验研究,而不是直接替代门控成像。根据信噪比(SNR)、分析比噪比(CNR)和基于图像的比噪比(IB-CNR)来评估系统性能。实验在限制光传播范围的1.2 m水箱中进行,在不同浊度条件和目标特性下进行。结果表明,成像性能在很大程度上取决于水衰减和物体特征,如反射率和表面纹理。在研究的配置中,浑浊水可以与反射目标的相对对比度的明显变化相关联,这降低了低反射率纹理物体的精细空间细节可见性;相比之下,清水能更好地保存高频信息。该研究证实了基于帧的CCD采集与探索性水下成像分析的相关性,并强调与时间门控系统的比较主要是基于模型的,而不是实验验证的,不应被解释为物理等效。
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引用次数: 0
Temporal Variations in the Elemental Composition and Size Distribution of Atmospheric Aerosol in South-East of Crimea in Spring and Summer 2020 2020年春夏克里米亚东南部大气气溶胶元素组成和粒径分布的时间变化
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700491
M. S. Artamonova, M. A. Iordanskii, O. G. Chkhetiani, V. A. Lapchenko, L. O. Maksimenkov

The problem of air pollution in Crimea is of interest due to its geographical characteristics and resort use. Experimental studies on the composition and temporal variability of aerosols in the surface air layer were conducted in the southeastern part of the Crimean Peninsula at the background environmental monitoring station of Vyazemsky Karadag Scientific Station—Nature Reserve, Branch of the Institute of Biology of South Seas, from March 21 to June 17, 2020. For the first time, data are presented on temporal variations in the daily average mass concentration of aerosol, chemical elements in its composition, and aerosol particles of 0.15–1.5 and 0.2–5.0 µm in size. Concentrations of 25 selected chemical elements are determined. The analysis is carried out depending on the direction of arrival of air masses. The elemental composition of the aerosol is compared with its size distribution, meteorological conditions, and the direction of long-range transport of air masses. The size of particles transporting heavy metals and metalloids (Zn, Mo, Cd, Pb, Bi, Se, Sn, and Sb), as well as elements of global origin is determined. The elements S, Cu, and Hg for which no significant correlation with the particle size was found, are likely of mixed origin due to competition between natural and anthropogenic sources in different periods. The results characterize the aerosol parameters during the spring–summer period in the eastern part of Crimea and are of interest to specialists involved in environmental monitoring in the resort and recreation area.

克里米亚的空气污染问题由于其地理特点和度假胜地的使用而引起人们的兴趣。2020年3月21日至6月17日,在南海生物研究所维亚泽姆斯基-卡拉达格科学站-自然保护区本底环境监测站,对克里米亚半岛东南部表层空气层气溶胶组成及时间变率进行了实验研究。首次获得了气溶胶的日平均质量浓度、组成中的化学元素以及粒径为0.15 ~ 1.5µm和0.2 ~ 5.0µm的气溶胶颗粒的时间变化数据。测定了25种选定的化学元素的浓度。根据气团到达的方向进行分析。将气溶胶的元素组成与其大小分布、气象条件和气团的远程输送方向进行比较。确定了携带重金属和类金属(Zn、Mo、Cd、Pb、Bi、Se、Sn和Sb)以及全球起源元素的颗粒大小。元素S、Cu和Hg与颗粒大小没有显著相关性,可能是由于不同时期自然和人为来源之间的竞争而产生的混合来源。这些结果描述了克里米亚东部春夏期间气溶胶参数的特征,并引起了度假区和娱乐区环境监测专家的兴趣。
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引用次数: 0
Temporal Variability of Carbon Dioxide and Methane Concentrations and their Stable Carbon Isotope Signatures in the Atmosphere over the Southern Taiga Zone of Western Siberia Derived from Observations at the Fonovaya Observatory in 2022–2024 西伯利亚西部南针叶林区大气中二氧化碳和甲烷浓度的时间变率及其稳定碳同位素特征——来自Fonovaya天文台2022-2024年的观测
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700594
M. Yu. Arshinov, V. G. Arshinova, B. D. Belan, D. K. Davydov, A. V. Kozlov

Seasonal and long-term variations in the atmospheric content of greenhouse gases is determined by their sources and sinks, which can be identified from the analysis of isotopic composition of these gases. This analysis can also help to understand the current upward trends in greenhouse gas concentrations on a regional scale. Based on continuous observations of atmospheric CO2 and CH4 and carbon isotope composition of their molecules at the Fonovaya observatory (Tomsk region) in 2022–2024, we estimate the ranges of background values and seasonal patterns of carbon isotope ratios δ13C–CO2 and δ13C–CH4 in the atmosphere above the southern taiga zone of Western Siberia. The daytime means (01–05 pm) of δ13C–CO2 and δ13C–CH4 ranged from −9.2 to −5.7‰ and from −51.7 to −46.5‰, respectively. The analysis of background values revealed a sharp minimum in CO2 concentration and a maximum in δ13C–CO2 in summer, which indicate active uptake of 12CO2 by regional terrestrial ecosystems. Winter values of CO2 concentration and δ13C–CO2 are consistent with data from other greenhouse gas monitoring stations in the Northern Hemisphere. The pattern of seasonal variations in atmospheric CH4 mixing ratios and δ13C–CH4 values in the region under study indicates that the winter maximum in CH4 content is driven by anthropogenic factors, while the summer maximum, by the predominance of biogenic methane emissions from Western Siberian wetlands. Using the Keeling plot method, source/sink signatures which affect changes in atmospheric CO2 and CH4 concentrations in the region under study were determined for each month of the year. The results can be used for analyzing and interpreting long-term observations of greenhouse gases in Siberia.

大气中温室气体含量的季节和长期变化是由它们的源和汇决定的,这可以通过分析这些气体的同位素组成来确定。这一分析还有助于了解当前区域尺度上温室气体浓度的上升趋势。利用托木斯克地区Fonovaya观测站2022-2024年连续观测的大气CO2和CH4及其分子碳同位素组成,估算了西西伯利亚南部针叶林带上空大气δ13C-CO2和δ13C-CH4碳同位素比值的背景值范围和季节特征。δ13C-CO2和δ13C-CH4的日间平均值(01-05 pm)分别在−9.2 ~−5.7‰和−51.7 ~−46.5‰之间。背景值分析显示,夏季CO2浓度急剧减小,δ13C-CO2急剧增大,表明区域陆地生态系统积极吸收12CO2。冬季CO2浓度和δ13C-CO2值与北半球其他温室气体监测站数据一致。研究区大气CH4混合比和δ13C-CH4值的季节变化特征表明,冬季CH4含量最大值受人为因素驱动,夏季最大值以西伯利亚西部湿地生物源性甲烷排放为主。利用基林图方法,确定了影响研究区域大气CO2和CH4浓度变化的源/汇特征。研究结果可用于分析和解释西伯利亚地区温室气体的长期观测。
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引用次数: 0
Numerical Analysis of Satellite Measurements of Nitrogen Dioxide in the Vicinity of a Large Thermal Power Plant 大型火力发电厂附近二氧化氮卫星测量数值分析
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S1024856026700582
V. F. Raputa, R. A. Kuzminykh, T. V. Yaroslavtseva

Methods for numerical interpretation of satellite measurements of nitrogen dioxide with the use of a model for reconstructing long-term regional pollution from a high-altitude point source of atmospheric emissions are discussed. The model is based on asymptotic representations of impurity concentration fields at significant distances from a source. Satellite measurements of nitrogen dioxide content in the region of the Gusinoozersk State District Power Plant (SDPP) were numerically analyzed. A high level of agreement was observed between satellite observations and model concentration fields for nitrogen dioxide emissions from SDPP pipes in the southwest and northwest directions. The analysis revealed the presence of significant nitrogen dioxide background concentrations caused by emissions from remote sources. The developed model also enables estimating the contributions of additional sources to NO2 concentration fields. The results can be used for estimating air pollutant emissions from thermal power plants from satellite data.

讨论了利用高海拔大气排放点源重建长期区域污染模型对卫星二氧化氮测量数据进行数值解译的方法。该模型基于离源显著距离处杂质浓度场的渐近表示。对Gusinoozersk州地区发电厂(SDPP)地区二氧化氮含量的卫星测量结果进行了数值分析。卫星观测值与模式浓度场在西南和西北方向上的SDPP管道二氧化氮排放高度一致。分析显示,由于来自偏远地区的排放,存在显著的二氧化氮本底浓度。所开发的模型还可以估算附加源对NO2浓度场的贡献。研究结果可用于根据卫星数据估算火电厂的大气污染物排放量。
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引用次数: 0
Laser-Induced Breakdown Spectroscopy of Liquid-Droplet Aerosols Using Nanosecond Pulses 基于纳秒脉冲的液滴气溶胶激光诱导击穿光谱研究
IF 0.7 Q4 OPTICS Pub Date : 2026-10-26 DOI: 10.1134/S102485602670048X
A. A. Ilyin, A. Yu. Mayor, Yu. S. Tolstonogova, V. V. Lisitsa

Laser-induced plasma diagnostics in aerosols is complicated by plasma inhomogeneity. In this work, the electron density of laser-induced plasma generated in liquid-droplet aerosol is evaluated based on Ba II 455.4, Na I 589, Al I 396.2, Ca II 393.4, and Fe I 542.4 nm emission lines for the case of using equipment on mobile carriers. It is found that the electron density is minimal for the Ba II line and maximal for the Na I line; the difference in the values reaches almost an order of magnitude, which is attributed to differences in the diffusion lengths of the elements. It is experimentally shown that the plasma electron temperature weakly depends on time in the range of 2–4 μs at exposure times of 40 and 150 μs. It is confirmed that recombination pumping of the upper levels of the transitions under study insignificantly affects the intensity of the analytical lines. Based on the analysis of the rate constants of excitation from the ground state, the limit of detection is found to be the worst for the Al I 396.2 nm line. The results of the work are in demand in emission spectral analysis of aerosols.

由于等离子体的不均匀性,激光诱导的气溶胶等离子体诊断变得复杂。在移动载体上使用设备的情况下,基于Ba II 455.4、Na I 589、Al I 396.2、Ca II 393.4和Fe I 542.4 nm发射谱线,对液滴气溶胶中产生的激光诱导等离子体的电子密度进行了评估。发现Ba II线的电子密度最小,Na I线的电子密度最大;数值的差异几乎达到一个数量级,这归因于元素扩散长度的差异。实验表明,当辐照时间为40和150 μs时,等离子体电子温度对时间的依赖性较弱,在2 ~ 4 μs范围内。证实了所研究的跃迁上层的复合抽运对分析谱线的强度影响不显著。通过对基态激发速率常数的分析,发现Al I 396.2 nm线的检测极限最差。研究结果在气溶胶发射光谱分析中有一定的应用价值。
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引用次数: 0
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