Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Fatty acid profiles of benthic environment associated with artificial reefs in subtropical Hong Kong

Artificial reefs can enhance habitat heterogeneity, especially in seabed degraded by bottom-dredging and trawling. However, the trophodynamics of such reef systems are not well understood. This study provided baseline data on trophic relationships in the benthic environment associated with artificial reefs in late spring and mid summer of subtropical Hong Kong, using fatty acid profiles as an indicator. Data from sediments collected at the reef base, materials from sediment traps deployed on top and bottom of the reefs, total particulate matter from the water column and oyster tissues from reef surface were subjected to principal component analysis. Results showed variations of fatty acid profiles in the total particulate matter, upper sediment trap and oyster tissue samples collected in the two samplings, indicating seasonal, trophodynamic changes within the reef system. The wastes produced by fish aggregating at the reefs can also contribute a source of biodeposits to the nearby benthic environment.     

Mathematical expressions used in amino acid racemisation geochronology—A review

A variety of mathematical expressions that describe changes over time (t) in the extent of amino acid racemisation (AAR, expressed as the ratio of d- to l-amino acid isomers or epimers) have been used in Quaternary geochronology. The integrated rate equation was first used to estimate fossil age from D/L but its geochronological utility is disadvantaged by uncertainties regarding the conformity of AAR in fossil protein to apparent reversible first-order kinetics for the entire reaction history. ‘Non-linear’ models have subsequently been used to relate D/L to t. The logarithmic equation successfully applied to Atlantic Coastal Plain research has not achieved widespread application, perhaps due to the regional calibration required if sensitivity to temperature is to be modelled, or the difficulties encountered when extending the model to include fossils with D/L<0.1. Success producing a linear correlation between D/L transformed with a power function and t has seen this approach emerge as one of the most commonly applied in AAR geochronology in recent years. Like parabola curve fitting, which has been applied to trends in D/L versus t in a variety of fossils and geographic settings, power transformations may not be suitable for geochronological modelling during the latter stages of amino acid diagenesis. Several studies have demonstrated the utility of simple and contingent linear equations for relating D/L to t. Future research should aim to reduce reliance on independent calibration and explore the geochronological benefits of AAR in pools other than the total hydrolysable amino acids.     

Characterization of low-molecular-weight organic acids isolated from the Toarcian argillite pore water (Tournemire site,France)

Bacterial activity in the near-field environment of radioactive waste disposal facilities in deep argillaceous rocks is currently under investigation. Bacterial development could be enhanced by the availability of low-molecular-weight organic acids (LMWOA) dissolved in the pore water of clayey rocks. This study firstly aimed at isolating and characterizing the LMWOA of the Toarcian argillite from the Tournemire Underground Research Laboratory (France, Aveyron). It also aimed at assessing the disturbing effects that could be induced by a disposal facility on the type and release of LMWOA (exposure to oxygen, alkaline pH, temperature increase). Under the experimental conditions investigated at 60 °C, the mean dissolved organic carbon (DOC) is about 15 mg L⁻¹ with a LMWOA proportion of 35 %. The main LMWOA are composed of formate, fumarate, propionate, acetate, and lactate. DOC is mainly influenced by both temperature and pH increases, whereas the LMWOA type nature and release are more specifically affected by the exposure to oxygen.     

连作马铃薯根系分泌物鉴定及其对尖孢镰孢菌(Fusarium oxysporum)的作用

为了揭示马铃薯连作化感物质与枯萎病之间的关系,通过水培和田间长期定位试验相结合方法,收集不同连作年限马铃薯根系分泌物,采用GC-TOF-MS进行分离鉴定.结果表明:在检测到的马铃薯根系分泌的48种物质中有机酸占30种.比较轮作、连作5年和连作10年马铃薯根系分泌物中有机酸的相对含量,发现苹果酸和棕榈酸的差异比较大.马铃...     

Formic and acetic acids in atmospheric condensate in Wilmington,North Carolina

Formic and acetic acids occurred in atmospheric condensate with concentrations similar to rainwater collected in Wilmington, North Carolina, during the sampling period from June to October of 1990. Atmospheric concentrations of these acids (calculated from the condensate concentrations) were higher in continental versus maritime air masses. Concentrations of formic and acetic acids were correlated with each other in both condensate and air. Traffic was a source of acetic acid and of bisulfite to atmospheric condensate in this study.     

Numerical study of the oxidation process of dimethylsulfide in the marine atmosphere

A box model, involving simple heterogeneous reaction processes associated with the production of non-sea-salt sulfate (nss-SO ₄ ^2– ) particles, is used to investigate the oxidation processes of dimethylsulfide (DMS or CH₃SCH₃) in the marine atmosphere. The model is applied to chemical reactions in the atmospheric surface mixing layer, at intervals of 15 degrees latitude between 60° N and 60° S. Given that the addition reaction of the hydroxyl radical (OH) to the sulfur atom in the DMS molecule is faster at lower temperature than at higher temperature and that it is the predominant pathway for the production of methanesulfonic acid (MSA or CH₃SO₃H), the results can well explain both the increasing tendency of the molar ratio of MSA to nss-SO ₄ ^2– toward higher latitudes and the uniform distribution with latitude of sulfur dioxide (SO₂). The predicted production rate of MSA increases with increasing latitude due to the elevated rate constant of the addition reaction at lower temperature. Since latitudinal distributions of OH concentration and DMS reaction rate with OH are opposite, a uniform production rate of SO₂ is realized over the globe. The primary sink of DMS in unpolluted air is caused by the reaction with OH. Reaction of DMS with the nitrate radical (NO₃) also reduces DMS concentration but it is less important compared with that of OH. Concentrations of SO₂, MSA, and nss-SO ₄ ^2– are almost independent of NO _x concentration and radiation field. If dimethylsulfoxide (DMSO or CH₃S(O)CH₃) is produced by the addition reaction and further converted to sulfuric acid (H₂SO₄) in an aqueous solution of cloud droplets, the oxidation process of DMSO might be important for the production of aerosol particles containing nss-SO ₄ ^2– at high latitudes.     

兰州市区酸雨及其生成机制

通过对１９９２ ～１９９４ 年１７９ 个降水过程的ｐ Ｈ 值分析发现,这３ 年期间兰州市区共出现了２１次酸雨,且酸雨出现次数占降水总次数的１１ ．７ ％ ;兰州市区酸雨主要发生在夏半年;兰州酸雨的形成与市区空气中高 Ｓ Ｏ２ 和 Ｎ Ｏ Ｘ 源密切相关。     

BOOK REVIEWS

Book Reviewed in this article: Marine Resources of Kuwait: Their Role in the Development of Non-oil Resources . Fatimah H. Y. al -Abdul -Razzak Recollections of a Revolution: Geography as Spatial Science . Mark Billinge , Derek Gregory and Ron Martin Entre l'Eden et l'Utopie . Luc Bureau Developments in Political Geography . M. A. Busteed The Elements of Graphing Data . William S. Cleveland Rural Resource Management . Paul J. Cloke and Chris C. Park Third World Atlas . Ben Crow and Alan Thomas Exploitation, Conservation, Preservation: A Geographic Perspective on Natural Resource Use . Susan L. Cutter , Hilary Lambert Renwick, and William H. Renwick . Wine Regions of the Southern Hemisphere . Harm Jan de Blij Regional Development: Problems and Policies in Eastern and Western Europe . George Demko The Geographer at Work . Peter R. Gould Change in the Amazon Basin . John Hemming Geography Since the Second World War . R. J. Johnston and P. Claval Urbanization in China: Town and Countryside in a Developing Economy 1949–2000 A.D. , R. J. R. Kirkby Transport and Communications for Pacific Microstates: Issues in Organisation and Management . Christopher C. Kissling Fluvial Forms and Processes . David Knighton The Urban Millennium . Josef W. Konvitz Technological Transition in Cartography . Mark Stephen Monmonier Field Guide to Soils and the Environment: Applications of Soil Surveys . Gerald W. Olson Northern Australia: The Arenas of Life and Ecosystems on Half a Continent . Don Parkes A Killing Rain: The Global Threat of Acid Rain . Thomas Pawlick From the Family Farm to Agribusiness: The Irrigation Crusade in California and the West, 1850–1931 . Donald J. Pisani Hybrid Maize Diffusion in Kenya . Franz -Michael Rundquist Warning and Response to the Mount St. Helens Eruption . Thomas F. Saarinen and James L. Sell Coastal Geomorphology in Australia . B. G. Thom Tropical Rain Forests of the Far East , 2nd ed . T. C. Whitmore The Dark Side of the Earth . Robert Muir Wood Categorical Data Analysis for Geographers and Environmental Scientists , Neil Wrigley