Effects of changing land use on dissolved organic matter in a subtropical river watershed, southeast China

The composition of dissolved organic matter (DOM) is an important determinant for its biogeochemical role in the aquatic environments. Therefore, it is crucial to determine the effects of changing land use on the DOM composition in the river watershed. Water samples were collected from the outlets of 15 sub-watersheds in the subtropical Jiulong River (southeast China) for fluorescence measurements and parallel factor analysis. Two humic-like (C1 and C2) and one protein-like (C3) fluorescent components were identified. Overall, DOM in the Jiulong River watershed was dominated by humic-like materials, probably due to the fact that 69% of the watershed is covered with forest. The 15 sub-watersheds were grouped into four clusters based on the proportion of each fluorescent component in the total fluorescence, suggesting that the DOM composition could be very different among sub-watersheds. There was a strong negative correlation between C2 and C3%. C1% correlated with the water body fraction, likely associated with the aquatic production of C1. C3% correlated positively with the residential area fraction, likely indicating the influence of anthropogenic activities. These results are useful for assessing the effects of land use/land cover changes on the composition and hence biogeochemical roles of DOM in aquatic environments.     

城市湖泊富营养化对水生植物叶片C、N、P化学计量特征的影响

为研究城市湖泊富营养化对水生植物叶片元素组成的影响,在植物生长季,对南京3个湖泊的6种常见水生植物进行碳(C)、氮(N)、磷(P)生态化学计量学研究,并分析驱动水生植物叶片元素变化的关键环境因子。结果表明:(1)水生植物叶片C、N、P含量变化范围分别为397.03～672.70、10.63～39.16及1.15～13.30 mg/g,叶片C/N、C/P及N/P变化范围分别为13.15～50.36、31.39～458.60及1.88～19.06,其中叶片P含量变异最大,叶片C含量变异最小;(2) Spearman相关性分析表明,芦苇(Phragmites australis)、睡莲(Nymphaea tetragona)和金鱼藻(Ceratophyllum demersum)叶片元素组成与湖泊富营养化综合指数具有显著相关性,叶片P含量随湖泊富营养指数升高而增加,叶片C/P及N/P随之减小;(3) RDA分析表明,春季水生植物叶片C、N、P含量及C/N/P变化主要受水体高锰酸盐指数(COD_(Mn))和底泥总有机碳(SOC)含量的共同影响,夏季主要受水体总磷(TP_W)浓度的影响,秋季主要受底泥总磷(TP_S)含量的影响。     

The molecular properties of humic substances isolated from a UK upland peat system: a temporal investigation.

The study concerns the possible changes in the molecular characteristics of humic materials isolated from the same source as a function of time. A great deal of data has been reported concerning the contrast in molecular characteristics of humic substances isolated from different environments. This has primarily been an attempt to identify source-specific molecular characteristics. However, data presented in this paper suggests that humic substances isolated from a single catchment have significant changes in molecular characteristics over time. Two naturally occurring peat pools (X and Y) situated upon a small organic catchment on Great Dun Fell, Cumbria, UK were sampled monthly between November 1994 and November 1996. Dissolved organic matter (DOM) from the pool water samples was fractionated using macroporous nonionic resins (XAD8 and 4), and the humic, fulvic and hydrophilic acids were collected. These fractions were analysed for elemental composition (C, H and N), weight average molecular weight, functional group content and adsorption (340 nm) of a 1 g l(-1) solution measured in a 1-cm spectrophotometer cell. The molecular characteristics were compared to those of natural DOM described by Scott et al. (1998). Scott et al. reported that drought conditions and seasonal climatic changes could have appreciable effects upon molecular characteristics of natural DOM. Results showed that the atomic H/C ratio of the humic substances increased immediately after strong drought conditions experienced in the summer of 1995. This change was temporary with atomic H/C ratio decreasing gradually over the following months. A similar decrease was observed in the carboxyl group content of the isolated compounds. The data set suggested that atomic H/C ratio in the fulvic and hydrophilic fractions exhibited seasonal characteristics of higher ratios during the late summer/early autumn months. This was not observed in the humic fraction. Humic acids exhibited a seasonal pattern of higher weight average molecular weight during the summer months. These trends were explained in terms of summer production of DOM in the catchment soils, their sequestering in the soil due to limited soil water movement during the summer months and their relative ease of dissolution when rainfall and soil water movement increased during the late summer/early autumn period. The results were found to support seasonal and long-term patterns observed in natural DOM as reported by Scott et al. (1998).     

水布垭水库水体碳时空变化特征及其影响因素分析

为了评估大型水库对河流碳循环的拦截作用,选择清江流域最上游水布垭水库为典型案例,采用德国元素公司vario TOC分析仪对定期采集水样进行分析,研究新建大型水库水体碳时空分布特征及其影响因素。结果表明,水布垭水库表层水体总碳、总无机碳、溶解有机碳和颗粒有机碳平均含量分别为26.665、24.089、2.141和0.438 mg/L,在水库年内蓄水阶段呈现显著的峰值,其空间分布格局在支流库湾和坝前典型断面表现出显著的差异,在水体碳中总无机碳占据主导地位,与湖泊水体碳时空分布特征极为相似。由于受到人类活动和自然环境的双重影响,水体无机碳则与水体电导率指标具有较强的相关性,溶解有机碳则与水体温度具有直接的关系,而数量最少的颗粒有机碳则与水体叶绿素含量具有弱相关关系。研究成果可以为理解水库碳循环过程机制提供数据支持,对于开展大坝建设的河流碳循环影响评估具有重要参考意义。     

Can ECOPATH with ECOSIM enhance models of radionuclide flows in food webs? An example for 14C in a coastal food web in the Baltic Sea

In this study it was evaluated whether the ECOPATH with ECOSIM software could be used as a platform to facilitate the construction of models and study of transport and accumulation of radionuclides in aquatic food webs. The evaluation was based upon a food web model of carbon (C) and carbon-14 ((14)C) flow for a coastal area in the Baltic Sea, the ECOPATH, the ECOSIM and the ECOTRACE models. The original carbon flows and assumptions were easily incorporated into the ECOPATH and ECOSIM modelling environment. The new model was also well suited to drive a (14)C flow model (ECOTRACE) for each of the organisms included. ECOTRACE estimated steady-state concentrations of (14)C that were between 73 and 142% of the original flows. The results clearly show that there is great potential for a successful development of this approach for integrating scientific knowledge about food webs and radioecological models for aquatic systems.     

The impact of land use on riparian soil dissolved organic matter and on streamwater quality on Chongming Island,China

Riparian wetland controls the transfer of terrestrial dissolved organic matter (DOM) to surface water bodies. However, the effects of land use on riparian soil DOM quality and its contribution to aquatic environment are largely unknown. In this study, the amount and composition of water-extracted soil organic matter (WSOM) in riparian wetlands were determined to evaluate the effect of land uses on spatial patterns of WSOM and streamwater quality on Chongming Island, China. The fluorescent properties of WSOM and fluvial DOM were analyzed using EEM spectra-combining PARAFAC model and accurate MS and MS/MS identification. Our findings showed no differences in the riparian WSOC contents between land use types (agricultural land, natural wetland, commercial land and industrial land). However, the fluorescent WSOM and its humic-like (Comp.1 and Comp.2) and microbial degradation (Comp.4) components significantly varied under different land uses (P < 0.05). Overall, the fluorescent WSOM quantities and its components (Comp.1, Comp.2 and Comp.4) were present at markedly lower concentrations for agricultural land use relative to the other three land uses. The same distribution pattern was observed for carbonyl compounds and fatty acids in the riparian WSOM molecules (P < 0.05), but the distribution patterns of the lipids were different between the four land uses (P < 0.05). Industrial land could result in the input of more organic matter into the riparian wetland. Our results showed that fluvial Comp.1 and Comp.2 were significantly correlated with WSOM Comp.2 and WSOM Comp.4 (P < 0.05). We also observed that the fluvial trophic status was significantly higher when the fluvial DOM components increased (P < 0.05). These results indicated that land uses can alter the composition of riparian WSOM, reshape fluvial DOM compositions and significantly affect fluvial water quality.     

香溪河流域不同介质中碳、氮、磷的分布特征及相关性研究

为了解香溪河流域碳、氮、磷的分布情况及水、陆生态系统中这些生源要素间的相互关系,对流域内河岸带土壤、河流水体及沉积物中总有机碳(TOC)、总氮(TN)、总磷(TP)含量进行调查,分析它们在流域内的分布特点,探讨各要素在3种介质间的相关性及随河流级别的变化规律。研究发现,超过60%的样点土壤中TOC、TN含量处于"较丰富"或"丰富"等级,耕地附近样点的TOC、TN和磷矿区附近样点的TP普遍偏高。河流水体及沉积物中各要素的含量都与土壤中的含量紧密相关,但水、陆介质间TP的相关性较TOC、TN强。低级别河流样点土壤中TOC、TN、C/P、N/P值和沉积物中C/P及N/P值整体较高级别河流样点高。结果表明:以磷矿开发和农业施肥为代表的人类活动,对香溪河流域内生源要素的含量及分布产生了显著影响;水体中P元素含量与陆源关系最强,在水体污染控制中应予以重视。     

The effects of exposure of 60Co on the oxidant/antioxidant status among radiation victims

This retrospective study has been performed with radiation victims who were accidentally exposed to a 60Co source and its release into the environment. The aim of the study was to assess the effects of elevated radiation exposures on plasma level, on erythrocyte thio barbituric acid reactive substance (TBARS) level and on erythrocyte glutathione (GSH) levels. Patients were treated in different hospitals with different symptoms such as nausea, vomiting, dizziness, along with severe anemia in some patients. Blood samples were collected 3-5 days following the radiation accident. Increases in plasma (6.25 +/- 0.90 nmol ml(-1)) and erythrocyte TBARS levels (330.5 +/- 30.5 micromol gHb(-1)) were found in comparison to a healthy group (3.72 +/- 0.68 nmol ml(-1) and 150.7 +/- 20.5 micromol gHb(-1), respectively) at a significant level (p<0.001). Erythrocyte GSH levels (5.2 +/- 0.30 micromol gHb(-1)) were found to be decreased among the victims (healthy group: 10.2 +/- 0.7 micromol gHb(-1)) at the same significance level (p<0.001). These observations confirm a significant change induced by radiation in the oxidant/antioxidant status among the victims. It is suggested here that antioxidant supplementation therapy might be effective in preventing the harmful effects of 60Co radiation among radiation victims.     

Uranium chemistry in stack solutions and leachates of phosphogypsum disposed at a coastal area in Cyprus

The effect of the matrix composition (main constituents) on the concentration and chemical behavior of uranium in phosphogypsum stack solutions and leachates has been investigated. Solid and aqueous samples were taken from three different sub-areas of a phosphogypsum stack at a coastal area in Vasilikos (Cyprus). The sub-areas are characterized whether by their acidity (e.g. "aged" and "non-aged" phosphogypsum) or by their salt content, originating from pulping water during wet stacking or (after deposition) from the adjacent sea. Measurements in stack solutions and leachates showed that phosphogypsum characteristics affect both, the concentration and the chemical behavior of uranium in solution. Uranium concentration in solutions of increased salinity is up to three orders of magnitude higher than in solutions of low salinity and this is attributed to the effect of ionic strength on the solubility of phosphogypsum. Modelling showed that uranium in stack solutions is predominantly present in the form of uranium(VI) phosphate complexes (e.g. UO(2)(H(2)PO(4))(2), UO(2)HPO(4)), whereas in leachates uranium(VI) fluoro complexes (e.g. UO(2)F(2), UO(2)F(3)(-)) are predominant in solution. The latter indicates that elution of uranium from phosphogypsum takes places most probably in the form of fluoro complexes. Both, effective elution by saline water and direct migration of uranium to the sea, where it forms very stable uranium(VI) carbonato complexes, indicate that the adjacent sea will be the final receptor of uranium released from Vasilikos phosphogypsum.     

Determination of non-steroidal anti-inflammatory drug (NSAIDs) residues in water samples

Pharmacologically active substances used to treat human and animal illnesses can enter the aquatic environment via effluents from wastewater treatment plants or in the case of veterinary drugs directly through liquid manure discharge. Some of these substances enter the environment either as the parent compound or as active/inactive metabolites. Due to their pharmacological activity, their determination and understanding their behavior and fate in the environment are important. The scope of this paper was to develop an analytical procedure to determine common pharmaceutical residues in wastewaters. Pharmacologically active substances were chosen according to their wide spread application in Slovenia and Central Europe and are members of analgesics, e.g., non-steroidal anti-inflammatory drugs: ibuprofen, naproxen, ketoprofen and diclofenac. Selected compounds were isolated from synthetic water using a novel SPE sorbent Strata X. Due to the non-volatile nature of these compounds they were first silylised prior to gas chromatographic-mass spectrometric detection. The developed procedure was tested with synthetic wastewaters and their extraction efficiency (>84%) and method limits of detection (2-6 ng L(-1)) were determined. Our procedure has been adopted and optimised for "real" water samples and applied to eleven drinking and ten river water samples from Slovenia. The results showed no traces of NSAIDs in all potable water samples and low-range contamination (ng L(-1)) of Slovene rivers. These results show that NSAIDs contamination of Slovene waters is comparable with published results of water contamination in Central Europe.     

水环境胁迫下的环鄱阳湖区城市化格局响应

当前城市化和水环境问题已成为全球共同面临的富有挑战性的问题,选取环鄱阳湖区作为研究样区,借助GIS技术,采用空间统计方法并建立水环境胁迫模型,对这种水环境胁迫下的城市化格局响应进行了研究。研究表明：（1）综合城市化计算显示,环湖区的城市化格局是随着与鄱阳湖体距离的增大,其城市化水平呈现出先增大后减小趋势,表明湖泊对城市化影响总体上显现出与距离相关的非线性分异格局;（2）空间统计结果显示,水资源富集的环湖核心区的空间关联比较显著,其水质对城市化水平的胁迫作用比较明显;（3）水胁迫度比较表明,在环湖边缘区和外围区水环境对城市化的胁迫强度级别有明显差异,随着与鄱阳湖体距离的增大,水环境对城市化的胁迫力也增大,表现出“中心 外围”逐渐增大的阶梯变化趋势     

Effects of seven organic pollutants on soil nematode Caenorhabditis elegans

Caenorhabditis elegans is a free-living soil nematode that is commonly used as a model for toxicity tests. The aim of this study was to investigate the toxicity of seven organic pollutants: four azaarenes (quinoline, acridine, phenazine, and 1,10-phenanthroline), short-chain chlorinated paraffins, and two organochlorinated pesticides (toxaphene and hexachlorobenzene). The exposure to all chemicals was carried out in three test media (soil, agar, and aquatic medium), and adult mortality was evaluated after 24 and 48 h. Toxaphene was the most toxic substance with LC(50) (48 h) of 379 mg/kg in the soil and 0.2 mg/L in the aquatic medium. Quinoline was the most toxic chemical in agar test with LC(50) (48 h) of 10 mg/L. HCB showed a very low toxicity in all tests, maybe due to its very low water solubility. Longer than 24-h test duration was found necessary for getting more correct data on toxicity. In comparison with other studies, C. elegans was less sensitive than other soil invertebrates. Different response might be attributed to different exposure routes and shorter test duration. Equilibrium partitioning theory was used to calculate K(oc) from results of soil and aquatic tests but this approach was found not working. Our results suggest that the tests with nematode C. elegans should be included to the battery of tests for risk assessment of POPs in soil.     

Quantifying summed fullerene nC60 and related transformation products in water using LC LTQ Orbitrap MS and application to environmental samples

The application of engineered nanomaterials increases strongly. Development of analytical techniques and their application to environmental samples is essential for human and environmental risk assessment of the nanoparticles. The objective of this study was to develop a sensitive analytical method to quantify nC(60) in water, using accurate mass screening liquid chromatography-hybrid linear ion trap Orbitrap mass spectrometry. nC(60) can be transformed by oxidation, reduction and photochemical reaction. Therefore, the formation of some transformation products of nC(60) was studied as well. Finally, the developed analytical method was applied to surface water samples from several locations in the Netherlands. The developed method enabled to detect and quantify aqueous concentrations of the summed nC(60) and its transformation products as low as 5 ng/L. It was observed that nC(60) transformation products exceed quantities of the parent C(60). Despite the high sensitivity of the developed method, no nC(60) or transformation products were detected in an array of Dutch surface waters. This might be due to low emissions, losses in the aqueous phase by sedimentation, sorption or further transformation processes.     

Radioisotope contaminations from releases of the Tomsk-Seversk nuclear facility (Siberia, Russia)

Soils have been sampled in the vicinity of the Tomsk-Seversk facility (Siberia, Russia) that allows us to measure radioactive contaminations due to atmospheric and aquatic releases. Indeed soils exhibit large inventories of man-made fission products including 137Cs (ranging from 33,000 to 68,500 Bq m(-2)) and actinides such as plutonium (i.e. 239+240Pu from 420 to 5900 Bq m(-2)) or 241Am (160-1220 Bq m(-2)). Among all sampling sites, the bank of the Romashka channel exhibits the highest radioisotope concentrations. At this site, some short half-life gamma emitters were detected as well indicating recent aquatic discharge in the channel. In comparison, soils that underwent atmospheric depositions like peat and forest soils exhibit lower activities of actinides and 137Cs. Soil activities are too high to be related solely to global fallout and thus the source of plutonium must be discharges from the Siberian Chemical Combine (SCC) plant. This is confirmed by plutonium isotopic ratios measured by ICP-MS; the low 241Pu/239Pu and 240Pu/239Pu atomic ratios with respect to global fallout ratio or civil nuclear fuel are consistent with weapons grade signatures. Up to now, the influence of Tomsk-Seversk plutonium discharges was speculated in the Ob River and its estuary. Isotopic data from the present study show that plutonium measured in SCC probably constitutes a significant source of plutonium in the aquatic environment, together with plutonium from global fallout and other contaminated sites including Tomsk, Mayak (Russia) and Semipalatinsk (Republic of Kazakhstan). It is estimated that the proportion of plutonium from SCC source can reach 45% for 239Pu and 60% for 241Pu in the sediments.     

Processes for sustainable development using high-intensity electric fields

Intense electric fields up to 10⁷ V/m generate very interesting and useful applications for the environment. Several processes using high electrical voltage for environment preservation were developed in the laboratory. The purpose of this study was to review these applications, highlighting their economic and environmental benefits: (1) electrostatic separators of particles used in industrial wastes recycling; (a) role-type electrostatic separator for granular mixtures of plastic–metal particles; (b) free-fall and rotating belt triboelectric separators for mixtures of plastic–plastic particles; (c) plate-type electrostatic separator for mixtures of metal–metal particles, (2) electrostatic precipitators for gas cleaning and (3) ozone generators for air and water treatment.     

Radiocarbon behaviour in seawater and the brown algae Fucus serratus in the vicinity of the COGEMA La Hague spent fuel reprocessing plant (Goury)--France

Extensive studies of the radiocarbon (14C) distribution and transfer in the marine environment of the North-Cotentin peninsula and along the English Channel have been carried out. The main aims of these studies have been to estimate the spatial and temporal variation of the 14C concentration in seawater and to calculate 14C concentration factors for some biological species. Such information will be helpful in order to calculate precisely radiation doses to humans. First results obtained in the vicinity of the COGEMA La Hague nuclear plant (Goury) indicate a 14C labelling of the dissolved inorganic carbon (DIC) in seawater (8.0-26.2 Bq.m(-3)) and a tight relationship between the 14C in the liquid releases from the plant and the 14C concentrations in DIC. The particulate organic carbon (POC) is also labelled. The concentration factor calculations for the brown algae (Fucus serratus) sampled from Goury, and also along the English Channel, give 14C values around 3000 Bq.kg(-1) fresh weight / Bq.L(-1).     

Distribution of pesticides, PAHs and heavy metals in prawn ponds near Kolleru lake wetland, India

This paper discussed the distribution of pesticides, polycyclic aromatic hydrocarbons (PAHs) and heavy metals in water, sediment and prawn from intensive prawn ponds (n=8) near the Kolleru lake wetland, India and assessed the quality of prawn for human consumption and also discussed the possible effects of these pollutants on pond environment and aquatic environment. The chemicals and other products used in prawn ponds near the Kolleru lake wetland were documented. The sediment, prawn and water samples were collected six times from selected prawn ponds during the production period of 3 months. Water samples were analyzed for selected physico-chemical parameters. The levels of pesticides, PAHs and heavy metals were found to decrease in the order sediment followed by prawn and water. The maximum concentrations of pesticides in sediment, prawn and water were alpha-BHC (174.2 microg g(-)(1)), gamma-BHC (234 microg g(-)(1)), malathion (256 microg g(-)(1)), chloripyrifos (198.5 microg g(-)(1)), endosulfan (238 microg g(-)(1)), dieldrin (19.6 microg g(-)(1)) and p,p'-DDT (128.6 microg g(-)(1)). Isodrin was found below detectable limit. The maximum concentrations of PAHs in sediment, prawn and water are anthracene (0.901 microg kg(-)(1)), fluranthene (0.601 microg kg(-)(1)), pyrene (0.786 microg kg(-)(1)), chrysene (0.192 microg kg(-)(1)), benzo(a)pyrene (0.181 microg kg(-)(1)) and benzo(ghi)perylene (227 microg kg(-)(1)). Benzo(e)pyrene, perylene, isomers of dibenzoanthracene and coronene were found below detectable limits. The maximum concentrations of heavy metals in sediment, prawn and water and also in prawn feed are Cu (791 microg g(-)(1)), Pb (270 microg g(-)(1)), Cd (1.07 microg g(-)(1)), Mn (4417 microg g(-)(1)), Ni (8.1 microg g(-)(1)), Co (5.8 microg g(-)(1)), Zn (1076 microg g(-)(1)), Cr (36.4 microg g(-)(1)), As (2.9 microg g(-)(1)), Se (6.3 microg g(-)(1)), Th (2.1 microg g(-)(1)) and Mo (0.762 microg g(-)(1)).     

Enhancement of AhR-mediated activity of selected pollutants and their mixtures after interaction with dissolved organic matter

Dissolved organic matter (DOM) in freshwaters is present at concentrations ranging from 0.5 to 50 mg L?1, and consists of various organic compounds, including humic substances (HS). HS exert a variety of direct and indirect biological effects, including interaction with the aryl hydrocarbon receptor (AhR). AhR is a cytosolic receptor that binds various hydrophobic organic compounds (HOCs) and mediates some of their toxic effects. In vitro effects of binary mixtures of various DOM (mainly HS) with various HOCs on AhR-mediated responses were studied by use of H4IIE-luc cells. Six out of 12 DOM activated the AhR even at environmentally relevant concentrations (17 mg L?1). In simultaneous exposures of H4IIE-luc cells to DOM (17 mg L?1) and each of the model compounds, 2,3,7,8-TCDD, PCB126, PCB169, benzo[a]pyrene, benzo[a]anthracene, dibenz[a,h]anthracene, fluoranthene, a mixture of persistent organic pollutants (POPs), a mixture of polycyclic aromatic hydrocarbons (PAHs), and a mixture of all HOCs, either significant additive or facilitative effects were observed when compared to activities of single HOCs. No significant decrease of effects due to possible sorption of HOCs to DOM was observed, even in subsequent experiments when HOCs+DOM mixtures were preincubated for six days before exposure to H4IIE-luc. Thus, DOM does not seem to protect organisms against AhR-mediated toxic effects of HOCs (as usually predicted due to sorption of HOCs on DOM), but it can actually enhance their potency for AhR-mediated effects in some situations.     

Characterisation, dissemination and persistence of gentamicin resistant Escherichia coli from a Danish university hospital to the waste water environment

The aim of the study was to investigate the potential spread of gentamicin resistant (GEN(R)) Escherichia coli isolates or GEN(R) determinants from a Danish university hospital to the waste water environment. Waste water samples were collected monthly from the outlets of the hospital bed wards and the inlet of the related waste water treatment plant (WWTP) from October 2002 to August 2003. Waste water samples were also collected monthly from a residential area in the same period to be able to compare the prevalence of GEN(R)E. coli isolates from hospital related and residential waste water. The waste water isolates were compared to GEN(R)E. coli isolates obtained consecutively from September 2002 to September 2003 from patients mainly with urinary tract infections at the hospital with respect to Pulsed Field Gel Electrophoresis (PFGE) profiles. All isolates were investigated for GEN(R) mechanisms (aac(3)-II, aac(3)-IV, ant(2')-I, armA), phenotypic resistance pattern, and virulence genes (hlyA, chuA, sfaS, fogG, malX, traT, iutA, fyuA, iroN, cnf1) to investigate if the hospital and waste water could be reservoirs of antimicrobial resistance and virulence. The ability for GEN(R) determinants to transfer horizontally was investigated by mating experiments. A total of 38, 15, 21, and two GEN(R)E. coli were isolated from patients, the hospital outlets, the inlet of the WWTP, and the residential area, respectively. GEN(R)E. coli were more prevalent in waste water from the hospital and the WWTP than in waste water from the residential area. PFGE profiling revealed no spread of specific patient isolates to the waste water. The aac(3)-II gene was detected both in patient and waste water isolates. Furthermore horizontal transfer of the aac(3)-II gene of patient origin to a recipient was shown in vitro, indicating a potential spread of the gene from patient isolates to waste water isolates. Regardless of origin, most isolates exhibited multi-resistance and contained several virulence genes. In conclusion, our study showed a possible spread of aac(3)-II from the hospital to the waste water. Most of the GEN(R)E. coli isolates from both patients and waste water had a multi-resistant phenotype and contained virulence genes and should therefore be considered reservoirs of antimicrobial resistance and virulence genes.     

宝天曼自然保护区土壤有机碳异质性及其影响因素

自然界中,土壤碳库对于维持生态系统碳平衡起决定性作用,而土壤有机碳又是碳库中不可或缺的一员,研究土壤有机碳对于全球生态系统碳平衡具有十分重大的意义。因此,基于宝天曼土壤有机碳实测数据并运用半方差函数、克里格插值分析山地土壤有机碳垂直性特征及空间分异程度,利用地理探测器对影响土壤有机碳分布的环境因子进行相关分析,结果表明:(1)宝天曼土壤有机碳介于0.31～7.7 g/kg,属于较低水平,最高值(7.70 g/kg)出现在北坡987 m处;(2)不同土层深度的半方差函数模型不同,0～20和40～60 cm对高斯模型拟合效果更明显、20～40 cm对球状模型拟合效果较好,而线性模型对于60～80和80～100 cm土层深度拟合效果较佳,克里格插值表明0～20和20～40 cm空间分异特征相似,呈西南向东北增加的趋势,而40～60 cm土壤有机碳空间分异呈现东北高、西南低;(3)宝天曼不同土层深度受单个环境因子影响程度不同,解释力介于0.127～0.407,其中NDVI对0～20 cm土壤有机碳解释力最显著(0.407)、高程对40～60 cm土壤有机碳解释力最高(0.373),交互探测结果表明NDVI与坡度解释力最高、高程与其他因子交互探测后解释力显著增大,表明宝天曼土壤有机碳受多种环境因子共同影响,而非单一因素起决定性作用。