92 resultados para 0.22 per mil
Residues of enrofloxacin, furazolidone and their metabolites in Nile tilapia (Oreochromis niloticus)
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The residues of enrofloxacin and its metabolite in Nile tilapia (Oreochromis niloticus) were studied after oral dose of 50 mg/kg for 7 days. To find the differences between Nile tilapia and Chinese shrimp (Penaeus chinensis), the residues of enrofloxacin in P chinensis were also studied under the same conditions. The results showed that enrofloxacin metabolized into ciprofloxacin in both Nile tilapia and P chinensis, the maximal concentration of enrofloxacin in muscle, liver and plasma of Nile tilapia were 3.61 mu g/g, 5.96 mu g/g, 1.25 mu g/ml respectively, and ciprofloxacin in muscle was 0.22 mu g/g. The maximal concentration of enrofloxacin and ciprofloxacin in P chinensis were 1.68 mu g/g and 0.07 mu g/g respectively. The predicted withdrawal time for Nile tilapia was 22 days, and P. chinensis was 12 days under our experiment conditions. The residues of fitrazolidone [3-(5-nitrofurfurylidenamino)-2-oxazolidinone] and its main metabolite 3-amina-2-oxazolidinone (AOZ) in Nile tilapia were first determined by HPLC/MS. Results showed that after oral dose of 30 mg/kg for 7 days, the maximum concentration of farazolidone in Nile tilapia was 413 mu g/kg after 6 h, whereas AOZ residue reached its maximum (31 mu g/kg) right after stopping treatment. In contrast to the high metabolic rate of furazolidone, AOZ was very difficult to eliminate in vivo, thus the withdrawal time of furazolidone in Nile tilapia was 22 days at least. (c) 2005 Elsevier B.V. All rights reserved.
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The hyphenated technique of high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry (HPLC-ICP-MS) was applied to the simultaneous determination of five organotin compounds (trimethyltin, dibutyltin, tributyltin, diphenyltin and triphenyltin) in seawater samples. Agilent TC-C18 column was used for the separation, the mobile phase of HPLC was CH3CN : H2O: CH3COOH=65 : 23 : 12 (phi), 0.05% TEA, and pH value was adjusted to 3.0 by diluent ammonia. The flow rate was 0.6 mL . min(-1). Five mixed organotin compounds in a mix standard solution from 100 to 0.5 mu g . L-1 were applied for the method assessment. The experimental results indicate that the correlation coefficient of calibration curves (R-2) for each organotin compound was over 0.998 and the detection limits of the five organotin compounds were lower than 3 ng . L-1. Different mixed organic solvents including dichloromethane or toluene were used for extraction of organotin and the extraction condition of organotin from seawater was optimized. The 100 mL seawater acidized by hydrochloric acid was extracted by 10 mL carbon dichloride (CH2Cl2) with 2% tropolone for 10 min twice. Extracted organic solvents were mixed And blown to one drop by nitrogen with the rate of 1.7 mL . min(-1), then 1 mL acetonitrile was added to the drop for redissolving the organotin compounds. Finally, the mixed redissolution was filtered by 0.22 mu m organic filter membrane before analysis. it was found that the only organotin compound in seawater was triphenyltin (TPHT) and the content was 53.2 ng . L-1. The recoveries test from the standard addition for diphenyltin (DPHT), dibutyltin (DBT), tributyltin (TBT) and triphenyltin (TPHT) were over 80%. However, the recovery for trimethyltin (TMT) was relatively low and the value was 50%. The reason might be attributed to the decomposition or adsorption of those compounds during the extraction procedure. Further study on this subject is in progress.
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,,CO_2,-,10,40.0%22.7%17.5%9.0%5.7%,62.7%
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120004104227.049Wm~(-1)4100.23590.22256%69428.6%68.0%3.4%37001900
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1999200268pelletsfood remains736281391424224114.26%40.79%17.39%26.99%0.22%0.35%33017774418322511.83%30.87%7.36%16.00%0.15%0.62%33.17%
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: (1) 14:00 (,) 1061 Wm-2 , 670218380 168 Wm-2 , 58 %20 %36 %14 % , 6 0. 22 ; (2) 91274 362 Wm-2 , 20 %38 %42 %; (3) , 20 :00 11 :00 , 01 :00 ; (4),
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, , 1314 h -158 499Wm- 2, 8 9 h 18 h , , 18 h 8 h , 13 h 49, 0.200.22, 0.24 0.49, 3d 0.25, 11h 15h 0.21
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We used an eddy covariance technique to measure evapotranspiration and carbon flux over two very different growing seasons for a typical steppe on the Inner Mongolia Plateau, China. The rainfall during the 2004 growing season (344.7 mm) was close to the annual average (350.43 mm). In contrast, precipitation during the 2005 growing season was significantly lower than average (only 126 mm). The wet 2004 growing season had a higher peak evapotranspiration (4 mm day(-1)) than did the dry 2005 growing season (3.3 mm day(-1)). In 2004, latent heat flux was mainly a consumption resource for net radiation, accounting for similar to 46% of net radiation. However, sensible heat flux dominated the energy budget over the whole growing season in 2005, accounting for 60% of net radiation. The evaporative rate (LE/R-n) dropped by a factor of four from the non-soil stress to soil water limiting conditions. Maximum half-hourly CO2 uptake was -0.68 mg m(-2) s(-1) and maximum ecosystem exchange was 4.3 g CO2 m(-2) day(-1) in 2004. The 2005 drought growing stage had a maximum CO2 exchange value of only -0.22 mg m(-2) s(-1) and a continuous positive integrated-daily CO2 flux over the entire growing season, i.e. the ecosystem became a net carbon source. Soil respiration was temperature dependent when the soil was under non-limiting soil moisture conditions, but this response declined with soil water stress. Water availability and a high vapor pressure deficit severely limited carbon fixing of this ecosystem; thus, during the growing season, the capacity to fix CO2 was closely related to both timing and frequency of rainfall events. (c) 2007 Published by Elsevier Masson SAS.
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Stable nitrogen isotope signatures of major sources of mineral nitrogen ( mineralization of soil organic nitrogen, biological N-2 fixation by legumes, annual precipitation and plant litter decomposition) were measured to relatively define their individual contribution to grass assimilation at the Haibei Alpine Meadow Ecosystem, Qinghai, China. The results indicated that delta N-15 values (- 2.40 parts per thousand to 0.97 parts per thousand) of all grasses were much lower than those of soil organic matter (3.4 +/- 0.18 parts per thousand) and mineral nitrogen ( ammonium and nitrate together,7.8 +/- 0.57 parts per thousand). Based on the patterns of stable nitrogen isotopes, soil organic matter (3.4 +/- 0.18 parts per thousand), biological N-2 fixation (0 parts per thousand), and precipitation (- 6.34 +/- 0.24 parts per thousand) only contributed to a small fraction of nitrogen requirements of grasses, but plant litter decomposition (- 1.31 +/- 1.01 parts per thousand) accounted for 67%.
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[1] The alpine meadow ecosystem on the Qinghai-Tibetan Plateau may play a significant role in the regional carbon cycle. To assess the CO2 flux and its relationship to environmental controls in the ecosystem, eddy covariance of CO2, H2O, and energy fluxes was measured with an open-path system in an alpine meadow on the plateau at an elevation of 3,250 m. Net ecosystem CO2 influx (Fc) averaged 8.8 g m(-2) day(-1) during the period from August 9 to 31, 2001, with a maximum of 15.9 g m(-2) day(-1) and a minimum of 2.3 g m(-2) day(-1). Daytime Fc averaged 16.7 g m(-2) day(-1) and ranged from 10.4 g m(-2) day(-1) to 21.7 g m(-2) day(-1) during the study period. For the same photosynthetic photon flux density (PPFD), gross CO2 uptake (Gc) was significantly higher on cloudy days than on clear days. However, mean daily Gc was higher on clear days than on cloudy days. With high PPFD, Fc decreased as air temperature increased from 10degreesC to 23degreesC. The greater the difference between daytime and nighttime air temperatures, the more the sink was strengthened. Daytime average water use efficiency of the ecosystem (WUEe) was 8.7 mg (CO2)(g H2O)(-1); WUEe values ranged from 5.8 to 15.3 mg (CO2)(g H2O)(-1). WUEe increased with the decrease in vapor pressure deficit. Daily albedo averaged 0.20, ranging from 0.19 to 0.22 during the study period, and was negatively correlated with daily Fc. Our measurements provided some of the first evidence on CO2 exchange for a temperate alpine meadow ecosystem on the Qinghai-Tibetan Plateau, which is necessary for assessing the carbon budget and carbon cycle processes for temperate grassland ecosystems.
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During the Devonian, a complicated carbonate platform-basin configuration was created through transtensional rifting in the context of opening of Devonian South China Sea; extensive bedded chert, commonly interbedded with tuffaceous beds, occurred in the narrow, elongate interplatform basins (or troughs) in South China, where they occurred earlier (Early Devonian) in southern Guangxi and later (early Late Devonian) in northern Guangxi-south central Hunan. In order to unravel the origin and distribution of the bedded chert successions, and their relationships to basement faulting activities during the opening of the Devonian South China Sea, studies of element (major, minor and REE) geochemistry and Rb-Sr, Sm-Nd isotopic systematics are carried out upon the chert deposits. These chert deposits commonly have high SiO2 contents and (average 94.01%) and low TFe2O3 (average 0.55%), together with other geochemical parameters, suggestive of both biogenic and hydrothermal origins. However, Fe/Ti ratio are high along the elongate interplatform basins(troughs) to the northwest along Wuxiangling-Zhaisha-Chengbu, and to the southeast along Xiaodong-Mugui-Xinpu, suggesting relatively intense hydrothermal activities there. They generally contain very low total REE contents (REE average 31.21ug/g) with mediate negative Ce anomalies (mean Ce/Ce*=0.83) and low Lan/Cen values (average 1.64), indicating an overall continental margin basin where they precipitated. The northward increases in Ce/Ce* values, particularly along the elongate troughs bounded both to the east and west of the Guangxi-Huanan rift basin, suggest a northward enhancement of terrigenous influences, thereby reflecting a gradual northward propagation of open marine setting. Generally low positive Eu anomalies in the chert, except for the apparently high Eu anomalies in the chert from Chengbu (Eu/Eu* up to 4.6), suggest mild hydrothermal venting activities in general, except for those at Chengbu. The initial 87Sr/86Sr (0) ratios of chert generally vary from 0.712000 to 0.73000 , suggesting influences both from terrigenous influx and seawater. The Nd isotopic model ages (tDM or t2DM) and initial Nd (0) values of chert vary mostly from 1.5 to 2.1 Ga, and from 16 to 21, respectively, implying that the silica sources were derived from the provenances of the Palaeoproterozoic crust relics at depth. The high Nd (0) values of chert (-0.22 to 14.7) in some localities, mostly along the elongate troughs, suggest that silica sources may have been derived from deeper-seated mantle, being channeled through the interplate boundary fault zones extending downwards to the mantle. At Wuxiangling, Nanning, chert occurs extensively from the Emsian through the Frasnian strata, both U/Th ratios and tDM ages of chert reached up to a maximum in the early Frasnian corresponding to the extensive development of chert in South China, pointing to a maximum extensional stage of Devonian South China basin, which is supported by the Ce/Ce* values as is opposed to the previous datasets as the coeval minimum values.
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In northern China, the loess-soil sequence of the last 2.6 Ma, the Hipparion Red-Earth of eolian origin and recently reported Pliocene-Miocene loess-soil sequence provide a near continuous continental eolian record of climatic history for the past 22.0 Ma. This work aims to investigate the composition and structure of clay minerals contained in deposits, and to explore their implications for environmental evolutions over the last 22.0 Ma. Clay minerals, which were extracted from eolian samples collected at Xifeng (0-6.2 MaBP) and Qinan (6.2-22.0 MaBP) sections, were analyzed qualitatively and semi-quantitatively by using X-ray diffraction (XRD), differential thermal analysis (DTA), thermogravimetric analysis (TG) and chemical analysis. The main conclusions are as follows: Over the last 22.0 Ma, the clay mineral assemblage among Quaternary loess-soils, Hipparion Red-Earth, and Miocene loess-soils shows similar components, mainly consisting of illite (55-80%), kaolinite (7-20%), chlorite (4-13%), smectite (2-23%) as results calculated by comparing major peak areas. There are no obvious differences in both types and amounts of clay minerals between loess and interbedded soils, suggesting that overwhelming part of the clay minerals is derived from the source. According to the components of clay minerals, the whole sequence of eolian deposits in the Loess Plateau can be divided into ten clay mineral assemblage zones over the last 22.0 Ma, whose corresponding ages are: 22.0-21.0 MaBP, 21.0-18.0 MaBP, 18-16.2 MaBP, 16.2-13.0 MaBP, 13.0-10.0 MaBP, 10.0-5.5 MaBP, 5.5-4.4 MaBP, 4.4-2.8 MaBP, 2.8-1.0 MaBP, 1.0-0 MaBP, respectively. This may imply that dust supply changed at least nine times over the past 22.0 Ma. The loess illite has a better crystaliinity, higher value of the FWHM and IC, than the interbedd soils. Previous studies indicated that irregular mixed layer minerals could form under relatively warm and humid conditions (Han, 1982). According to the general distribution of clay minerals of zonal soil (Chamley, 1989), the clay mineral assemblage of eolian deposits in Xifeng and Qinan sections is typical of temperature-humid and warm-subarid environment. Therefore, our results indicate climatic environment in Loess Plateau did not change remarkably since 22.0 Ma, and fluctuated between temperature-humid and warm-subarid climate. 4. The illite generally presents poorer crystaliinity during the period of 22.0 to 2.8 MaBP than in the last 2.8 Ma BP, especially at the intervals of 3.5-4.5 Ma BP, 14.0-17.0 MaBP and 20.0-22.0 Ma BP, which indicates that the weathering intensity was stronger in Neogene than in Quaternary. 5. The relatively low ice volume and high global temperature may be responsible for the strange weathering intensity during the interval of the 3.5-4.5 Ma BP, 14.0-17.0 Ma BP and 20.0-22.0 Ma BP.
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,240 Pu/ 239 Pu ,: 240 Pu/ 239 Pu 0. 240. 31 ,240 Pu/ 239 Pu 0. 220. 24 ,0. 18 240 Pu/ 239 Pu ,50 ,,55 %40 %20 %,
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.,.,MgOTiO2,Al2O3.,(logfO2)680740-16.00-15.31,530650-19.20-17.50.,.,log(fH2O/fHF)fluid,log(fH2O/fHCl)fluid,log(fHF/fHCl)fiuid4.224.39,2.783.24,-1.82-1.73,log(fH2O/fHF)fluid,log(fH2OfHCl)fluid,log(fHF/fHCl)fluid3.273.53,2.853.22,-0.75-0.22,,ClSn.,.ClSn..
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2005320058 1. (HgT)2.1~19.5 ng•L-19.3ng•L-1(HgD)1.7~ 9.0 ng•L-14.1ng•L-1(HgP)0.3~14.8 ng•L-15.2 ng•L-1(HgR)0.1~ 4.5 ng•L-11.7 ng•L-1 2. 3.- 4. 0cm8cm10cm 5. 160-252 ng•g-1209 ng•g-10.22-7.21 ng•g-11.76 ng•g-1 6. pH7.5-8.57.1-47.9 ng•L-10.16-2.50 ng•L-10.25-2.43ng•L-1<
