History of atmospheric environment

There have been great transitions in the science of air pollution and science publishing since the journal began as the International Journal of Air Pollution in 1958. Atmospheric Environment witnessed the increased understanding of smog photochemistry in the late 1950s and the emerging fears of ozone depletion in the 1970s. The journal has grown, but not without the need to change and occasionally fragment only to reintegrate at a later date. At 9000 pages a year it represents an enormous editorial task that has had to be undertaken by more professional offices. This transition has been helped through the development of electronic tools, but the editorial offices strive to retain their personal relationship with authors and reviewers. An enhanced international perspective recognises the widening contributions made by scientists beyond Europe and North America.     

The effect of precipitation on the vertical profiles of atmospheric ammonia: A modeling investigation

This paper describes theoretical calculations of atmospheric ammonia profiles during precipitation events. The PLUVIUS reactive storm model (Hales, 1982, Atmospheric Environment16,1775–1783) was used in a simplified form relevant to this specific system. Calculated NH₃ profiles for dry atmospheres were consistent with distributions previously reported in the literature. NH₃ profiles in the gas and cloud phases, following a simulated convective storm, showed large variations with height. These variations are strongly dependent on storm duration. In some cases, NH₃ gas concentrations were depleted by more than 50% by the precipitation scavenging process. Modeled NH₃ gas profiles regenerate slowly with time after storm termination.     

环境科研论文撰写与发表的方法和策略

概要地介绍了中文环境科技核心期刊、美国《工程索引》（EI）和《科学引文索引》（SCI）收录中国科研论文的情况，以及两份知名英文环境期刊的论文评审标准。EI和SCI收录其来源期刊中英文摘要符合要求的论文。一篇好英文摘要有助于论文被国际环境期刊录用和增加论文的影响力。基于目前EI及SCI的来源期刊中缺少中文专业期刊，国内的环境科研人员可以先将其重要研发成果陆续在中文环境核心期刊上发表，形成系列文章，然后再融合这些文章，投寄英文国际环境期刊。这个策略可及时将研发成果公开发表，提高论文被国际期刊录用的几率，并增加中文环境核心期刊的知名度和声望。     

An investigation of the formation of ambient NH4NO3 aerosol

The aerosol equilibrium formulation of Stelson and Seinfeld (1982a, b, Atmospheric Environment16, 983–992, 993–1000) is incorporated into the STEM-II transport/chemistry model and is evaluated against NH₃, HNO₃ and aerosol NH₄⁺ and NO₃⁻ measured at Nagano Prefecture, Japan on 29 and 30 July 1983. These results indicate that this modeling approach is useful in analyzing field data.     

Diffusion of an instantaneous cluster of particles in homogeneous turbulence

In this work we study the diffusion of instantaneous puffs vs the diffusion of continuous plumes. The model which we use is a Lagrangian model for the motion of N particles suggested by Kaplan and Dinar (1988, J. compt. Phys. 79, 317–335). This model is based on the approach of Richardson to the relative diffusion which states that the instantaneous relative velocity of particles is a function of their instantaneous separation. Results show that the diffusion of a puff is slower than that of a continuous source. We find that the puff evolves more slowly than in the analytic model of Lee and Stone (1983, Atmospheric Environment17, 2477–2481), since in their model diffusion is influenced only by the initial conditions. The effect of the source size on the diffusion rate is studied as well.     

Calculating mean concentrations for steady sources in recirculating wakes by a particle trajectory method

A discrete vortex model of the recirculating flow behind a two-dimensional backward-facing step is used to calculate the trajectories of particles released from a fixed point. By averaging over a large number of such trajectories, an estimate is made of the mean concentration profile associated with a steady source in the wake. These estimates are verified against experimental data for point- and line-sources. The importance of incorporating a ‘random walk’ in calculating the trajectories is demonstrated. The mean flow in the discrete vortex model used appears to be the most critical factor in determining mean concentrations. The poorest predictions appear to be associated with the longest trajectories.Particle ‘recirculation times’ are also briefly examined and it is shown how these are related to the ‘residence times’ of Vincent (1976, Atmospheric Environment11, 765–774) and others. It is suggested that such residence times may not be an appropriate means of quantifying near-wake dispersion if sources are inside the wake. Advantages of a ‘particle trajectory’ method, as against a diffusion equation method, for dealing with dispersion in inhomogeneous flow are finally presented.     

Stability of two prediction schemes for hourly nitrogen oxide concentrations by a regression model

In a preceding paper (Inoue et al, 1986b, Atmospheric Environment20, 2325–2337), we proposed two prediction schemes for hourly nitrogen oxide (NO) concentration using the regression model with autocorrelated error terms, and applied these schemes to the prediction of NO-concentration at m h later. Data analyses based on the data sets observed at a measurement site for a year showed that these schemes are practical for the predictions 1 h later.In this follow up paper, we apply these schemes to the prediction for other years and/or other measurement sites, and investigate the stability of the assumed regression model and the adopted prediction schemes not only numerically but also theoretically. From these analyses, our prediction schemes are shown to be stable for the prediction of NO-concentration in other years.     

A photochemical model for air quality assessment: Model description and verification

A hybrid Eulerian-Lagrangian, photochemical model has been developed for the assessment and prediction of the impact of large point sources on air quality. This simple model is based on solving the mass conservation equations which include chemical reaction terms in the cells of a two-dimensional crosswind plane which moves with the air parcel. Testing of the model is done in three ways. First, the chemistry is evaluated using results of smog chamber experiments simulating Melbourne's emissions and meteorological conditions. Second, the accuracy of the emissions inventory is tested using aircraft measurements. Finally the overall performance of the model is evaluated using monitoring station data. In general the model gives good agreement with the measurements, with the predictions for O₃ being somewhat better than those for NO₂. This result was also found in the three-dimensional study of McRae and Seinfeld (1983, Atmospheric Environment17, 501–522) for the Los Angeles area.     

The kernel method for air quality modelling—II. Comparison with analytic solutions

The performance of Lorimer's (1986) kernel method (Atmospheric Environment20, 1447–1452) for solving the advection-diffusion equation is tested for instantaneous and continuous emissions into a variety of model atmospheres. Analytical solutions are available for comparison in each case. The results indicate that a modest minicomputer is quite adequate for obtaining satisfactory precision even for the most trying test performed here, which involves a diffusivity tensor and wind speed which are nonlinear functions of the height above ground. Simulations of the same cases by the particle-in-cell technique are found to provide substantially lower accuracy even when use is made of greater computer resources.     

Nucleation of sulfuric acid-water and methanesulfonic acid-water solution particles: Implications for the atmospheric chemistry of organosulfur species

Binary nucleation theory is applied to the formation of aqueous sulfuric acid and aqueous methanesulfonic acid particles and the relative rates of aerosol formation in humid atmospheres are compared. An integral model is presented which describes nucleation of solution particles, aerosol growth, and condensable vapor source and depletion rates. To extend this model, the water activities of the ternary solution, sulfuric acid-methanesulfonic acid-water, are estimated, and growth of the nucleated aerosol by incorporation of both types of acid is considered. Predictions of both forms of the model are compared with the experimental results of Hatakeyama et al. [Atmospheric Environment19, 135–141 (1985)] for the photooxidation of dimethylsulfide in humid air.     

Modeling distributions of air pollutant concentrations—II. Estimation of one and two parameter statistical distributions

In Part I of this series Taylor, Jakeman and Simpson (1986, Atmospheric Environment, 20, 1781–1789) examined the problem of identifying the appropriate distributional form for air pollution concentration data. In this paper we examine the parameter estimation problem. Monte Carlo simulation is used to compare methods for fitting statistical distributions to such data where the distributional form is known. Three methods are investigated for estimating the parameters of the lognormal distribution, two methods for the exponential distribution, three methods for the γ-distribution and four methods for the Weibull distribution. For all distributions and for each method we examine the accuracy with which the upper percentiles of the distribution are evaluated as it is these percentiles which are referred to by air quality standards. For each distribution a simple empirical model, which yields approximations to the relative root mean square error of the percentile estimates against sample size and parameter values, is developed and demonstrated. Thus for each distributional model an estimate of the relative error associated with evaluating high pollutant levels may be readily determined.     

Stochastic simulation of meteorological variability for long-range atmospheric transport—II. Long-term statistical models

Methods are developed for simulating meteorological inputs for statistical atmospheric transport models. Stochastic models are presented for the annual mean wind vector, the horizontal diffusion coefficient, the fraction of time it is raining, and the quantity of precipitation. The models are derived by aggregating the statistical models for short-term meteorological processes given in the companion paper of Small and Samson (Atmospheric Environment, 1989, 23, 2813–2824). Normal distributions are used for each variable. The normal distribution is derived directly for the mean wind vector based on the normality of short-term winds, and serves as an acceptable approximation for the other variables given their low interannual coefficient of variation. Correlation between variables is considered, including correlation between winds and precipitation, between the fraction of time it is raining and the total quantity of precipitation at a site, and between the annual precipitation quantity at multiple sites. Development and confirmation of the interannual distributions is supported by long-term meteorological data, including a nine-year backward trajectory record computed for a site in western Pennsylvania. Application of the method is demonstrated with a statistical atmospheric LRT model used to predict distributions of annual precipitation sulfates in eastern North America. Predicted interannual coefficients of variation of wet SO₄²⁻ concentrations range from about 10 to 15 per cent, similar to the level of interannual variation inferred from long-term data sets.     

Acidic deposition distribution and episode statistics from the MAP3S network database

Data for precipitation and acidic pollutant concentration from the MAP3S network in the eastern United States were analyzed to assess the probability distributions of acidic deposition and the spatial and temporal character of high deposition events (or ‘episodes’). About 20% of the precipitation events account for about 55% of the deposition of the major species (sulfur, nitrate, free hydrogen, and ammonium). The mean ‘episodicity’, as defined by Smith and Hunt (Atmospheric Environment12, 461–477, 1978), is 7%; this is not considered highly episodic. The distribution characteristics are spatially quite uniform over the MAP3S region, suggesting a homogeneous pollution-exposure environment. Occurrences of the leading deposition events generally follow the seasonal trends in concentration, and the major episodes usually account for about 10% or less of a given year's total deposition. Most episode events are characterized by above-normal values of both precipitation amount and concentration.     

Comparative analysis of chemical reaction mechanisms for photochemical smog—II. Sensitivity of EKMA to chemical mechanism and input parameters

The six chemical reaction mechanisms for photochemical smog described in Pan I (Leone and Seinfeld, 1985, Atmospheric Environment 19,437–464) were used to study the effect of input parameters on volatile organic compound (VOC) control requirements needed to meet the National Ambient Air Quality Standard for ozone. The parameters studied were initial VOC composition, dilution rate, post 8-a.m. emissions, base case (present day) O₃ levels, entrainment from aloft of VOC and ozone and initial VOC/NO_x ratio. The Empirical Kinetic Modeling Approach (EKMA) was used to generate ozone isopleths for each chemical mechanism. The VOC control needed to reduce the maximum ozone concentration from some present day value to 0.12 ppm, assuming no NO_x control and a specified initial VOC/NO_x ratio, was calculated using the six chemical reaction mechanisms. The initial VOC/NO_x ratio was found to have the largest effect of all the parameters studied on VOC control requirements. Choice of chemical mechanism, ozone and VOC entrainmem from aloft, base-case ozone and the composition of the initial VOC mixture also had a large effect on predicted control requirements. To reduce the degree of uncertainty in control predictions using EKMA it is necessary to establish as accurately as possible the composition of urban air in early morning. Also, because of the substantial effect the choice of chemical mechanism has on the predicted control requirements using EKMA, it is important that future work continues to be directed toward evaluating candidate chemical mechanisms with respect to their ability to simulate atmospheric smog chemistry.     

Using of “pseudo-second-order model” in adsorption

A research paper's contribution exists not only in its originality and creativity but also in its continuity and development for research that follows. However, the author easily ignores it. Citation error and quotation error occurred very frequently in a scientific paper. Numerous researchers use secondary references without knowing the original idea from authors. Sulaymon et al. (Environ Sci Pollut Res 20:3011–3023, 2013) and Spiridon et al. (Environ Sci Pollut Res 20:6367–6381, 2013) presented wrong pseudo-second-order models in Environmental Science and Pollution Research, vol. 20. This comment pointed the errors of the kinetic models and offered information for citing original idea of pseudo-second-order kinetic expression. In order to stop the proliferation of the mistake, it is suggested to cite the original paper for the kinetic model which provided greater accuracy and more details about the kinetic expression.     

Measured isoprene emission rates of plants in California landscapes: comparison to estimates from taxonomic relationships

Isoprene emission rates of 64 plant species found in California's urban and natural landscapes were measured using a dynamic flow-through chamber enclosure technique. Species were selected to provide data for previously unmeasured species and to test estimates of isoprene emission rates based upon taxonomic relationships developed for compilation of biogenic emission inventories as proposed by Benjamin et al. (1996, Atmospheric Environment 30, 1437–1452). Branch-level isoprene emission rates ranged from undetectable for 47 species, to 54 μg g⁻¹ h⁻¹ for Quercus kelloggii, California black oak. Isoprene emission rate estimates based on taxonomy agreed well with our measurements for species within the same genus, with the exception of the Quercus genus for which a wide range of isoprene emission rates have been reported. As expected, family-level estimates based on taxonomy showed greater deviation from our measured values than did genus-based estimates. The data developed in the present study support use of a taxonomic predictive methodology, especially if previous measurements within specific families, sub-families, and genera are extensive, and the results of such assignment are treated with proper caution. A taxonomic approach may be most useful where plant species in natural and urban landscapes are numerous, such as in California, where no experimental measurements are available for thousands of species.     

Toxic Substances in the Atmospheric Environment Discussion

The Critical Review on Toxic Substances in the Atmospheric Environment was presented by Bernard D. Goldstein at the 76th Annual Meeting of the Air Pollution Control Association in Atlanta, Georgia. Dr. Goldstein summarized his paper, which had been published in the May 1983 issue of JAPCA. Prepared discussions presented at the Critical Review Session are reproduced here. In addition, comments made from the floor and through the mails have been formalized and are published along with closing remarks by Dr. Goldstein. Dr. Paul J. Lioy served as Moderator for the 1983 Critical Review Session.     

A Special Issue from the NARSTO Symposium on Tropospheric Aerosols

This dedicated issue of the Journal of the Air & Waste Management Association contains nine peer-reviewed scientific papers that were presented at the NARSTO Symposium on Tropospheric Aerosols: Science and Decisions in an International Community, held October 24-26, 2000, in Querétaro, Mexico.¹ Other peer-reviewed papers^2-9 appear in a companion issue of Science of the Total Environment to be published in February 2002. More than 130 papers were presented in platform and poster sessions at the meeting. Approximately 28% of the technical presentations dealt with topics from Mexico, and 15% related to Canada, with the remainder discussing U.S. and global topics.