Determination of some organochlorine pesticide residues in honeys from Konya, Turkey

In this study, 24 organochlorine pesticide residues in 109 different honey samples collected from stores and open markets in Konya, Turkey were analyzed by gas chromatography-electron capture detection. Aldrin, cis-chlordane, trans-chlordane, oxy-chlordane, 2,4^′ -DDE, and 4,4^′ -DDE were found in all honey samples. The mean value was 0.0540 μg g^???1 for oxy-chlordane. In the 55 samples of 109, levels of organochlorine pesticide residues of oxy-chlordane were determined as higher than those of Turkish Alimentarius Codex maximum residual limits (MRLs). Other organochlorine pesticide residues also exceeded MRLs except for cis-heptachlor epoxide and α-hexachlorocyclohexane. Since all of the honey samples are found contaminated and most of these samples exceeded MRLs, a control of organochlorine pesticide residues in honey is necessary for consumer health.     

Variations of measured and simulated soil-loss amounts in a semiarid area in Turkey

The main goal of this research was soil-loss determination and comparison of the plot measurement results with simulation model (universal soil loss equation (USLE)) results in different land use and slope classes. The research took place in three different land-use types (Scotch pine forest, pasture land, and agricultural land) and in two different slope classes (15–20%, 35–40%). Within six measurement stations (for each land-use type and slope class-one station), totally 18 measurement plots have been constituted, and soil-loss amount measurements have been investigated during the research period (3 years along). USLE simulation model is used in these measurement plots for calculation the soil-loss amounts. The results pointed out that measured (in plots) and simulated (with USLE) soil-loss amounts differ significantly in each land-use type and slope class.     

In vitro activity of antimicrobial agents against Legionella isolated from environmental water systems: first results from Turkey

We evaluated the in vitro activity of antimicrobial agents against Legionella obtained from hotel and hospital water systems in three different regions of Turkey. Sixty-five Legionella strains (Legionella pneumophila serogroup 6 [n?=?32], L. pneumophila serogroup 1 [n?=?27], L. pneumophila serogroup 3 [n?=?2], and Legionella spp. [n?=?4]) were tested against levofloxacin, ciprofloxacin, clarithromycin, azithromycin, and rifampicin. The minimum inhibitory concentration (MIC) values of each antimicrobial agent for these strains was determined by the microdilution method using buffered yeast extract medium supplemented with 0.1% ketoglutarate broth. L. pneumophila ATCC 33152, Staphylococcus aureus ATCC 29213, and Escherichia coli ATCC 25922 were used as controls. Minimum inhibitory concentration values were in the following ranges: clarithromycin 0.001–0.5 mg/L, azithromycin 0.001–0.5 mg/L, levofloxacin 0.001–0.5 mg/L, ciprofloxacin 0.001–0.125 mg/L, and rifampicin 0.001– 0.5 mg/L. The MIC₉₀ for rifampicin, levofloxacin, ciprofloxacin, azithromycin, and clarithromycin were 0.015, 0.125, 0.06, 0.125, and 0.06 mg/L, respectively. To the best of our knowledge, this is the first study to determine in vitro activities of antimicrobial agents against Legionella species in Turkey. Rifampicin had the lowest MIC₉₀ value. It would seem that azithromycin and clarithromycin exhibit good activity as well as levofloxacin and ciprofloxacin against Legionella isolated from environmental water systems in Turkey.     

The comparison of heavy metal accumulation ratios of some fish species in Enne Dame Lake (Kütahya/Turkey)

The metal accumulation levels for muscle, skin, gill, liver and intestine tissues of some Cyprinidae species (Carassius carassius, Condrostoma nasus, Leuciscus cephalus and Alburnus alburnus) in Enne Dame Lake (Kütahya/Turkey), which is mostly fed by hot spring waters, were investigated. Analyses were performed for copper (Cu), zinc (Zn), manganese (Mn), iron (Fe), cobalt (Co), magnesium (Mg), nickel (Ni), chrome (Cr) and boron (B) using inductively coupled plasma-optic emission spectroscopy (ICP-OES), and cadmium (Cd) using atomic absorption spectrophotometer (AAS) utilizing microwave digestion techniques. The concentrations of the heavy metals found in the fish varied in the follow ing ranges: Cu: < DL-7.04, Zn: 6.96-357.25, Mn: < DL-20.70, Ni: < DL-6.21, Fe: 9.62-2500.33, Cr: < DL-1.74, Co: < DL-0.54, Cd: 0.01-0.27 and Mg: 197.44-904.90 mg/kg wet weight. While B had the second highest concentration in the water of the lake, it was not encountered in any tissue of the investigated species. In all tissues and the species, While the bioaccumulation factors (BAFs) of Mn, Zn, Fe and Cu were remarkably high, the BAFs of Mg, Cr, Co, and B were also fairly low or none. Although the heavy metal accumulation levels for the muscle were generally lower than other tissues, there were some exceptions. Cd level in the muscle of C. carassius was higher than the permissible limit stated by Turkish legislation, FAO and WHO. The mean metal amounts for all the investigated tissues and species are statistically compared and discussed in this study.     

Solid phase extraction of Cu(II), Ni(II), Pb(II), Cd(II) and Mn(II) ions with 1-(2-thiazolylazo)-2-naphthol loaded Amberlite XAD-1180

A new method for separation and preconcentration of trace amounts of Cu(II), Ni(II), Pb(II), Cd(II) and Mn(II) ions in various matrices was proposed. The method is based on the adsorption and chelation of the metal ions on a column containing Amberlite XAD-1180 resin impregnated with 1-(2-thiazolylazo)-2-naphthol (TAN) reagent prior to their determination by flame atomic absorption spectrometry (FAAS). The effect of pH, type, concentration and volume of eluent, sample volume, flow rates of sample and elution solutions, and interfering ions have been investigated. The optimum pH for simultaneous retention of all the metal ions was 9. Eluent for quantitative elution was 20 ml of 2 mol l(-1) HNO(3). The optimum sample and eluent flow rates were found as 4 ml min(-1), and also sample volume was 500 ml, except for Mn (87% recovery). The sorption capacity of the resin was found to be 0.77, 0.41, 0.57, and 0.30 mg g(-1) for Cu(II), Ni(II), Cd(II), and Mn(II), respectively. The preconcentration factor of the method was 200 for Cu(II), 150 for Pb(II), 100 for Cd(II) and Ni(II), and 50 for Mn(II). The recovery values for all of the metal ions were > or = 95% and relative standard deviations (RSDs) were < or = 5.1%. The detection limit values were in the range of 0.03 and 1.19 microg l(-1). The accuracy of the method was confirmed by analysing the certified reference materials (TMDA 54.4 fortified lake water and GBW 07605 tea samples) and the recovery studies. This procedure was applied to the determination of Cu(II), Ni(II), Pb(II), Cd(II) and Mn(II) in waste water and lake water samples.     

云南腾冲地区大气降水中氢氧稳定同位素特征

为了揭示腾冲地区降水中氢氧稳定同位素特征,利用2009年1月～2011年12月腾冲地区339个降水样品资料,对降水中的氢、氧同位素组成及其影响因素进行了分析和研究。结果表明：腾冲地区大气降水中δ18O值变化范围为-2678‰～405‰,δD值变化范围为-20095‰～3689‰,均处于全球降水δ18O与δD值变化范围内。天气尺度下,腾冲地区降水中δ18O的变化具有显著的降水量效应以及反温度效应。但是,在季风降水期间,如果相邻两天都有降水发生时,腾冲地区降水中δ18O值变化并不一定遵循“降水量效应”。利用ECMWF（European Centre for Medium Range Weather Forecasts）提供的TCWV（Total Column Water Vapour）再分析资料,发现TCWV与δ18O的日变化存在明显的反位相对应关系。腾冲地区的大气降水线为：δD=818δ18O+1172,斜率与截距均比全球和全国的大气降水线偏大,说明该地区气候湿润多雨。d值分布具有季节差异,在雨季（4～9月）,腾冲地区降水的水汽主要来源于低纬度海洋,空气湿度大,降水中d值较小;在干季（10～3月）,由于受大陆性气团控制,腾冲地区降水的水汽主要来源于西风带的输送以及局地再蒸发水汽的补充,空气湿度小,降水中d值较大     

基于遥感数据的PM2.5与城市化的时空关系研究——以成渝城市群为例

采用1998~2013年卫星遥感影像反演的PM2.5全球高精度产品数据集,结合GIS空间分析、地理加权回归（GWR）以及地理探测器等方法,系统地分析了成渝城市群城市化与PM2.5分布之间的关系。结果表明：（1）1998~2013年成渝城市群城市化速度较快,城市区域的PM2.5均值明显高于非城市区域,说明城市化对PM2.5具有一定的影响;（2）近16 a PM2.5重心与城市重心整体上都向东南方向移动,且两者每年在经度上的波动方向基本相反;（3）夜间灯光数据与PM2.5在空间分布上具有较好的一致性,且1998~2013年两者的GWR全局R2在0.86~0.95之间,相关性显著,研究区内城市化和人类活动对PM2.5的分布具有明显影响;（4）地理探测分析表明不同城市化因子对PM2.5影响差异显著,从2006到2013年城区人口密度和建成区绿化覆盖率逐渐成为成渝城市群PM2.5分布的主要影响因子。     

Radiological hazard assessment of natural gross radioactivity in some cosmetic products

Many kinds of cosmetic products were analyzed to determine gross radioactivity. In this study, gross alpha/beta radioactivity concentrations in 51 cosmetic samples were determined. The examined cosmetic products consist of blusher, eye shadow, lipstick, nail polish, shampoo, hand cream, cellulite cream, baby powder, soap, and toothpaste. The gross alpha–beta activity concentrations were measured with a nuclear spectroscopic system which contains gas-flow proportional counters. The highest gross alpha/beta activity concentrations were found in eye shadow samples of 1.621Bq g^?1 for alpha and 6.471Bq g^?1 for beta. The total effective doses due to gross radioactivity for skin were calculated. Although the effective dose of eye shadow samples had the highest value, the effective doses due to gross radioactivity concentrations in this study were found to be lower than the radiological limits given by the authorities.     

Prenatal diagnosis of autosomal recessive osteopetrosis,infantile type,by X-ray evaluation

Prenatal diagnosis for infantile osteopetrosis was attempted during the third pregnancy of a first-cousin marriage whose family history revealed an affected previous child. At the 25th week of pregnancy, fetal X-ray evaluation revealed marked sclerosis of osteopetrotic bone and metaphyseal splaying and clubbing of both femurs. The pregnancy was terminated and repeated X-rays and histopathological examination of fetal bone (femur) confirmed the diagnosis.