Kinetics of the reaction of nitrogen dioxide with ozone

The kinetics of the reaction of NO₂ with O₃ have been investigated at 296 K, using UV absorption spectroscopy to monitor decay of NO₂ or O₃ and infrared laser absorption spectroscopy to monitor formation of the reaction product N₂O₅. The results both for the rate coefficient at 296 K (k ₁=3.5×10^-17 cm³ molecule^-1 s^-1) and the reaction stoichiometry (NO₂/O₃=1.85±0.09) are in good agreement with previous studies, confirming that the two step mechanism involving formation of symmetrical NO₃ as an intermediate is predominant.% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaeOtaiaab+% eadaWgaaWcbaGaaeOmaaqabaGccqGHRaWkcaqGpbWaaSbaaSqaaiaa% bodaaeqaaOWaa4ajaSqaaaqabOGaayPKHaGaaeOtaiaab+eadaWgaa% WcbaGaae4maaqabaGccqGHRaWkcaqGpbWaaSbaaSqaaiaabkdaaeqa% aaaa!41D7!\[{\text{NO}}_{\text{2}} + {\text{O}}_{\text{3}} \xrightarrow{{}}{\text{NO}}_{\text{3}} + {\text{O}}_{\text{2}} \]% MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGaaeOtaiaab+% eadaWgaaWcbaGaae4maaqabaGccqGHRaWkcaqGobGaae4tamaaBaaa% leaacaqGYaaabeaakiabgUcaRiaab2eadaGdKaWcbaaabeGccaGLsg% cacaqGobWaaSbaaSqaaiaabkdaaeqaaOGaae4tamaaBaaaleaacaqG% 1aaabeaakiabgUcaRiaab2eaaaa!4464!\[{\text{NO}}_{\text{3}} + {\text{NO}}_{\text{2}} + {\text{M}}\xrightarrow{{}}{\text{N}}_{\text{2}} {\text{O}}_{\text{5}} + {\text{M}}\]A possible minor role for the unsymmetrical ONOO species is suggested to account for the lower-than-expected stoichiometry factor. The importance of this reaction in the oxidation of atmospheric NO₂ is discussed.     

保持空间分布特征的散列式居民地综合选取方法

中小比例尺地形图上存在大量由不依比例尺"房屋群"构成的散列式居民地,综合选取时除考虑单个房屋专题重要性外,还要保持各房屋群的分布特征。将基于Vorinoi图模型的点群化简算法应用到散列式居民地选取中,在综合选取的两个主要过程(选取定额模型和结构化选取方法)中综合考虑分布密度、分布范围等分布结构信息和专题属性信息。实验分析表明,该方法保留重要居民地的同时,能够较好地保持原有的空间分布特征。     

菲对斜生栅藻(Scenedesmus obliquus)自由基的诱导及胁迫效应

通过静态模拟实验,研究不同浓度(0.005、0.01、0.025、0.05和0.1 mg/L)菲暴露96 h后,对斜生栅藻的生长、自由基含量、抗氧化系统以及脂质过氧化产物(MDA)的影响.结果表明,0.01 mg/L菲开始对藻细胞生长产生显著抑制作用,在此浓度下电子自旋共振检测到的自由基信号(g=2.0033,幅宽10.15 mT)显著增强;在浓度设置范围内,超氧化物酶歧化酶、过氧化物酶、谷胱甘肽-S-转移酶活性均被显著诱导,显示出抗氧化系统的应激机制.谷胱甘肽和MDA含量均在0.025 mg/L时被显著诱导.这说明斜生栅藻对菲暴露比较敏感,0.01 mg/L即已显示胁迫效应,自由基的诱导是斜生栅藻产生损伤的重要原因,藻细胞的生长量是比较敏感的损伤指标.     

Dynamics and fluxes of organic carbon and nitrogen in two Guiana Shield river basins impacted by deforestation and mining activities

Deforestation and mining activities have proven to be very damaging to rivers because these activities disturb the environmental characteristics of rivers. Thus, the concentrations of dissolved organic carbon (DOC), particulate organic carbon (POC), particulate nitrogen (PN), and Chlorophyll‐a (Chl‐a) were measured monthly during 2 hydrological years in the Maroni and Oyapock Rivers to assess the dynamics and fluxes of organic carbon and nitrogen in these 2 Guiana Shield basins, which have been strongly (Maroni) and weakly (Oyapock) impacted by deforestation and mining activities. The 2‐year time series show that DOC, POC, PN, and Chl‐a concentrations vary seasonally with discharge in both rivers, indicating a hydrologically dominated control. Temporal patterns of DOC, POC, and PN indicate that these variables show maximum concentrations in rising waters due to the yield of organic matter and nitrogen accumulated in soils, which are incorporated into the rivers during rainfall. However, the Chl‐a concentrations were at a maximum during low‐water stages. The C/N and C/Chl‐a ratios also showed a seasonal trend, with lower values during the low water periods due to an increase in algal biomass. During high water, the POC in both rivers is the result of terrestrial organic matter, whereas during low‐water autochthonous organic matter can reach up to 34% of the POC. The mean annual fluxes of TOC and PN were higher (4.56 × 10⁵ tonC year^?1 and 1.77 × 10⁴ tonN year^?1, respectively) in the Maroni River than those (1.84 × 10⁵ tonC year^?1 and 0.54 × 10⁴ tonN year^?1, respectively) in the Oyapock River. However, the specific fluxes of DOC, POC, and PN from both basins were nearly the same. Although gold mining activities are performed in both basins, there is no conclusive evidence regarding the impact of these activities on the dynamics of organic matter and particulate nitrogen in the Maroni and Oyapock Rivers.     

Measurements of nighttime nitrate radical concentrations in the atmosphere by long-path differential optical absorption spectroscopy

The long-path differential optical absorption spectroscopy(LP-DOAS)technique was developed to mea- sure nighttime atmospheric nitrate radical(NO_3)concentrations.An optimized retrieval method,resulting in a small residual structure and low detection limits,was developed to retrieve NO_3.The time series of the NO_3 concentration were collected from 17 to 24 March,2006,where a nighttime average value of 15.8 ppt was observed.The interfering factors and errors are also discussed.These results indicate that the DOAS technique provides an essential tool for the quantification of NO_3 concentration and in the study of its effects upon nighttime chemistry.     

东海黑潮地转流计算中的零流面选取问题

零流面的选取是东海黑潮地转流计算中的一个基本问题。通过对东海黑潮主流段PN断面上选取不同零流面时地转流计算结果的比较分析,考虑了东海黑潮的主要特征因子,确定了计算零流面的选取标准和选择结果。结果表明,为使计算结果可以反映实际的流速剖面结构,当水深大于700 m和小于700 m时可分别选取700 m层和底边界作为地转流动力计算零流面。     

Hydroxyl Radical Concentrations Estimated from Measurements of Trichloroethylene during the EASE/ACSOE Campaign at Mace Head, Ireland during July 1996

During the EASE/OXICOA campaign of the NERC ACSOE programme, trichloroethylene and a wide range of man-made halocarbons and radiatively-active trace gases were monitored with high precision and high frequency throughout July 1996 at Mace Head on the Atlantic Ocean coast of Ireland. Trichloroethylene concentrations in concert with many other trace gases became elevated as regionally-polluted and photochemically-aged air masses reached Mace Head. However, as the anticyclonic air masses retreated during 19 and 20 July, trace gas concentrations remained elevated for a significant period. During this 2–4 day period, trichloroethylene concentrations decayed significantly, though the concentrations of the other more chemically-inert trace gases did not. A detailed interpretation of this behaviour using a Lagrangian dispersion model has allowed the estimation of average and peak OH radical concentrations of 3 and 9×10⁶ molecule cm^-3, respectively, during the travel from the source areas in the U.K. and the low countries out to Mace Head. Using a simple box model, the available Mace Head measurements, when combined into a detailed chemical mechanism, generated OH radical concentrations which peaked at 7×10⁶ molecule cm^-3, in close agreement with the estimates based on trichloroethylene decay.     

贻贝棘尾虫年轻与衰老无性系抗氧化能力的比较

贻贝棘尾虫采自黑龙江省帽儿山南山水库附近水塘,于１９９５年９月在本系实验室通过接合生殖得到的接合后体,克隆培养作为无性系;采用１９８８年９月以来实验室保存培养的去小核无性系为衰老无性系。     

Studies on free radical scavenging activity in Chinese seaweeds part I. Screening results

INTRODUCTIONIthaslongbeenknownthatfatsundergoslowautoxidationduringstorage;andthatantioxidantswhichscavengefreeradicalsexistingduringtheinitialstageorearlypropagationstageoflipidoxida tioncanpreventrancidity ,soantioxidantsareoftenusedasfoodadditivescapableofdelaying ,re tardingorpreventingtherancidityinlipidsduetooxidation .Inthissense ,anidealantioxidantshouldhavethefollowingcharacteristics:safeinuse ,noodor,flavororcolor,effectiveatlowcon centration ,easytoincorporateandavailableatlowco…     

Impact of halides on the photobleaching of dissolved organic matter

Understanding absorbance photobleaching of marine dissolved organic matter (DOM) is important because DOM chromophores impact oceanic primary productivity by affecting the depth of the photic zone, absorb UV radiation and affect ocean color used in remote sensing. However, the fundamental mechanisms which account for this bleaching are largely unknown. Controlled laboratory studies demonstrated that the presence of seawater concentrations of chloride and bromide ions enhanced absorbance photobleaching reaction rates by ~ 40%, regardless of DOM source or the presence or absence of carbonate ions. In contrast, halide ions generally did not affect fluorescence bleaching rates. Variations in ionic strength did not alter the enhancement in absorbance photobleaching by halide ions. Accordingly, the enhancement in absorbance photobleaching was specific to halide ions, rather than a generalized salinity effect. We confirmed the formation of hydroxyl radical (HO^•) in illuminated samples, and its significant scavenging in the presence of halide salts. Gamma-radiolysis experiments and associated modeling indicated that a small component (~ 12%) of the photobleaching enhancement by halides was consistent with the hypothesis that halide scavenging of HO^• will form reactive halogen radicals that target electron-rich chromophores within DOM more selectively than HO^•. The mechanism responsible for the major component of absorbance photobleaching rate enhancement by halides remains unresolved.