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1.
微生物参与下的氮循环是富营养化湖泊十分重要的生物地球化学循环过程.采用基于amoA功能基因和16S rRNA基因的荧光定量PCR、PCR-DGGE与高通量测序等分子生物学技术,调查秋季太湖不同水体和表层沉积物中氨氧化古菌(AOA)、氨氧化细菌(AOB)和亚硝酸盐氧化菌(NOB)群落丰度和组成,探讨影响硝化微生物分布的关键环境因子.结果表明,中度富营养化的梅梁湾湖区水体表层、中层和底层水样和表层底泥中AOA amoA基因的丰度分别低于轻度富营养化的湖心区,而不同层水样中AOB amoA基因的丰度分别高于湖心区.梅梁湾湖区和湖心区水样中AOA群落组成基本相似,2个湖区表层沉积物样品中AOA群落组成亦基本相似,水体中AOA群落组成与表层沉积物中AOA群落组成有差异,AOA群落丰度显著受硝态氮、pH和DO影响;表层沉积物中AOB群落丰度有明显差异且显著受总氮含量影响,表层沉积物中NOB群落丰度也有明显差异且显著受亚硝态氮含量影响.太湖梅梁湾湖区和湖心区水体与表层沉积物AOA群落包括Nitrosopumilium和Nitrosotalea两大属;表层沉积物AOB群落主要包括亚硝化单胞菌(Nitrosomonas)和亚硝化螺菌(Nitrosospira)两大属,NOB群落主要包括硝化刺菌(Nitrospina)和硝化螺菌(Nitrospira)两大属,其中硝化螺菌属是淡水湖泊中比较少见的亚硝酸盐氧化菌.影响太湖水体和沉积物中AOA和AOB丰度的最主要环境因子为总氮、总磷与铵态氮.研究表明典型富营养指标(总氮、总磷、铵态氮、硝态氮和硝态氮等)是影响太湖梅梁湾和湖心区水体和沉积物中AOA或AOB丰度以及硝化微生物群落丰度的重要因素.  相似文献   

2.
In this study, the effect of sludge retention time on ammonia oxidizing bacteria (AOB) and nitrite oxidizing bacteria (NOB) in an anaerobic/oxic (AO) process, was explored. The results indicated that the growth rate constants of AOB were 0.97, 0.88, and 0.79 d–1, respectively, meanwhile, those of NOB were 1.22, 1.03, and 0.93 d–1, respectively, when the sludge retention time (SRT) was 15 days, 10 days and 5 days. The relation between the growth rate constant and the SRT could be best described using a simple exponential curve and a second type hyperbolic curve. The lysis rate constants for AOB and NOB were 0.13 and 0.18 d–1, respectively. The yield coefficients values of AOB and NOB were 0.22 and 0.21, respectively. The percentage of AOB to mixed liquid suspended solids (MLSS) was 0.64%, 0.53%, and 0.35%, respectively. Meanwhile, the percentage of NOB was 2.24%, 1.87%, and 1.11%, respectively, at SRT values of 15 days, 10 days and 5 days. When the SRT value decreased, the AOB and NOB biomass levels decreased by 12.75 and 47.01 mg L–1, respectively. Meanwhile the removal efficiency of NH4+‐N decreased from 90 to 26%, while the removal efficiency of total nitrogen (TN) decreased from 14 to 8%.  相似文献   

3.
Subduction‐related volcanic rocks are widespread in the Central Pontides of Turkey, and represented by the Hamsaros volcanic succession in the Sinop area to the north. The volcanic rocks display high‐K calc‐alkaline, shoshonitic and ultra‐K affinities. 40Ar/39Ar age data indicate that the rocks occurred during the Late Cretaceous (ca 82 Ma), and the volcanic suites were coeval. Primitive mantle‐normalized trace element patterns of all the lavas are characterized by strong enrichments in large ion lithophile elements (LILE) (Rb, Ba, K, and Sr), Th, U, Pb, and light rare earth elements (LREE; La, Ce) and prominent negative Nb, Ta, and Ti anomalies, all typical of subduction‐related lavas. There is a systematic increase in the enrichment of incompatible trace elements from the high‐K calc‐alkaline lavas through the shoshonitic to the ultra‐K lavas. In addition, the shoshonitic and ultra‐K lavas have significantly higher 87Sr/86Sr (0.70666–0.70834) and lower 143Nd/144Nd (0.51227–0.51236) initial ratios than coexisting high‐K calc‐alkaline lavas (87Sr/86Sr 0.70576–0.70613, 143Nd/144Nd 0.51245–0.51253). Geochemical and isotopic data show that the shoshonitic and ultra‐K rocks cannot be derived from the high‐K calc‐alkaline suite by any shallow level differentiation process, and point to a derivation from distinct mantle sources. The shoshonitic and ultra‐K rocks were derived from metasomatic veins related to melting of recycled subducted sediments, but the high‐K calc‐alkaline rocks from a lithospheric source metasomatized by fluids from subduction zone.  相似文献   

4.
Banded iron formations are the most characteristic of Archean–Paleoproterozoic sediment records. Laminated textures resembling banded iron formations can be observed in modern hot‐spring environments. Using sedimentological and microbiological techniques, we investigated the processes of laminar formation and considered the origin of lamination textures. An iron‐rich deposit at the Okuoku‐hachikurou hot spring in Japan exhibits sub‐millimeter laminations consisting of bacteria‐induced ferrihydrite and aragonite. The ferrihydrite particles are spherical and exhibit fine lamination, up to 100 µm thick in ferrihydrite‐rich parts. In aragonite‐rich parts, ferrihydrite particles form filamentous textures with diameters of 10–30 µm, but not laminations. Textural analysis using scanning electron microscopy and phylotype analysis using 16S rRNA indicated the bacterial contribution to ferrihydrite precipitation. A sheath‐like fabric showing a meshwork of nanometer‐order organic filaments, and sheath‐forming bacteria were observed in the deposit specimen etched by citric acid. Phylotype analysis detected in the iron‐rich deposits some bacterial types related to cyanobacteria, purple bacteria, and iron‐oxidizing bacteria. Iron‐oxidizing bacteria probably were responsible for precipitation of the ferrihydrite. Chemolithoautotrophic iron‐oxidizing bacteria are microaerophilic and thrive on Fe(II) in a redox gradient, but dissolved oxygen was not detected in the Okuoku‐hachikurou hot spring. Thus, a certain supply of oxygen is needed for metabolism of the microaerophilic iron‐oxidizing bacteria. The distribution of photosynthetic pigments in the iron‐rich parts indicates that the most likely source of oxygen is photosynthesis by cyanobacteria. This symbiotic relationship between cyanobacteria and iron‐oxidizing bacteria can explain the laminated texture of iron‐rich deposits in the Okuoku‐hachikurou hot spring. These laminations may reflect changes in photosynthetic intensity. There is presently some debate about the bacterial groups that may have played roles in precipitation of banded iron formations. This study presents a new bacterial model for iron precipitation and may provide a mechanism for sub‐millimeter laminations in banded iron formations deposited in shallow water.  相似文献   

5.
The effects of plant species richness (SR; i.e., 1, 2, 4, 8, and 16 species per plot) on substrate nitrate and ammonium retention and ecosystem productivity in a full‐scale constructed wetland (CW) with high nitrogen (N) input were studied. Substrate nitrate (0.1–16.4 mg kg?1) and ammonium concentrations (1.3–9.2 mg kg?1) in this study were higher than those in other comparable biodiversity experiments. Substrate nitrate concentration significantly increased while ammonium concentration significantly decreased with the increase of plant SR (p = 0.008 and 0.040, respectively). The response of ecosystem productivity to increasing SR was unimodal with four species per plot achieving the greatest productivity. Transgressive overyielding, which was compared to the most productive of corresponding monocultures, did not occur in most polycultures. We conclude that substrate N retention was enhanced by plant SR even with high N input, and plant SR could be managed to improve the efficiency of N removals in CWs for wastewater treatment.  相似文献   

6.
Whole‐rock geochemical and Sr–Nd isotopic data are presented for late Miocene volcanic rocks associated with the Chah Zard epithermal Au–Ag deposit in the Urumieh‐Dokhtar Magmatic Arc (UDMA), Iran, to investigate the magma source, petrogenesis and the geodynamic evolution of the study area. The Chah Zard andesitic to rhyolitic volcanic rocks are characterized by significant Large Ion Lithophile Element (LILE) and Light Rare Earth Element (LREE) enrichment coupled with High Field Strength Element (HFSE) depletion. Our geochemical data indicate an adakitic‐like signature for the volcanic rocks (e.g. SiO2 > 62 wt%, Al2O3 > 15 wt%, MgO < 1.5 wt%, Sr/Y > 70, La/Yb > 35, Yb < 1 ppm, and Y < 18 ppm, and no significant Eu anomalies), distinguishing them from the other volcanic rocks of the UDMA. The Chah Zard volcanic rocks have similar Sr and Nd isotopic compositions; the 87Sr/86Sr(i) ratios range from 0.704 902 to 0.705 093 and the εNd(i) values are from +2.33 to +2.70. However, the rhyolite porphyry represents the final stage of magmatism in the area and has a relatively high 87Sr/86Sr ratio (0.705 811). Our data suggest that the andesitic magmas are from a heterogeneous source and likely to result from partial melting of a metasomatized mantle wedge associated with a mixture of subducted oceanic crust and sediment. These melts subsequently underwent fractional crystallization along with minor amounts of crustal assimilation. Our study is consistent with the model that the volcanic host rocks to epithermal gold mineralization in the UDMA are genetically related to late Miocene Neo‐Tethyan slab break‐off beneath Central Iran.  相似文献   

7.
Talat  Ahmad  Kabita C.  Longjam  Baishali  Fouzdar  Mike J.  Bickle  Hazel J.  Chapman 《Island Arc》2009,18(1):155-174
The Sakoli Mobile Belt comprises bimodal volcanic rocks that include metabasalt, rhyolite, tuffs, and epiclastic rocks with metapelites, quartzite, arkose, conglomerate, and banded iron formation (BIF). Mafic volcanic rocks are tholeiitic to quartz‐tholeiitic with normative quartz and hypersthene. SiO2 shows a large compositional gap between the basic and acidic volcanics, depicting their bimodal nature. Both the volcanics have distinct geochemical trends but display some similarity in terms of enriched light rare earth element–large ion lithophile element characteristics with positive anomalies for U, Pb, and Th and distinct negative anomalies for Nb, P, and Ti. These characteristics are typical of continental rift volcanism. Both the volcanic rocks show strong negative Sr and Eu anomalies indicating fractionation of plagioclases and K‐feldspars, respectively. The high Fe/Mg ratios for the basic rocks indicate their evolved nature. Whole rock Sm–Nd isochrons for the acidic volcanic rocks indicate an age of crystallization for these volcanic rocks at about 1675 ± 180 Ma (initial 143Nd/144Nd = 0.51017 ± 0.00017, mean square weighted deviate [MSWD] = 1.6). The εNdt (t = 2000 Ma) varies between ?0.19 and +2.22 for the basic volcanic rock and between ?2.85 and ?4.29 for the acidic volcanic rocks. Depleted mantle model ages vary from 2000 to 2275 Ma for the basic and from 2426 to 2777 Ma for the acidic volcanic rocks, respectively. These model ages indicate that protoliths for the acidic volcanic rocks probably had a much longer crustal residence time. Predominantly basaltic magma erupted during the deposition of the Dhabetekri Formation and part of it pooled at crustal or shallower subcrustal levels that probably triggered partial melting to generate the acidic magma. The influence of basic magma on the genesis of acidic magma is indicated by the higher Ni and Cr abundance at the observed silica levels of the acidic magma. A subsequent pulse of basic magma, which became crustally contaminated, erupted as minor component along with the dominantly acidic volcanics during the deposition of the Bhiwapur Formation.  相似文献   

8.
In this study the occurrence of diclofenac and sub‐products in effluent emerging from the University Hospital at the Federal University of Santa Maria was investigated. One metabolite was identified and, in aqueous solution, three degradation products. The quantification was conducted by means of HPLC‐DAD, and the determination of metabolite and degradation products by LC–ESI–MS/MS–QTrap. For the HPLC‐DAD method, a 70:30 mixture of methanol/sodium phosphate was used in isocratic mode. For the LC–ESI–MS/MS–QTrap determinations, a mobile phase, where phase A was an ammonium acetate solution 5 × 10?3 mol L?1, and phase B was methanol (5 × 10?3 mol L?1)/ammonium acetate (9:1, v/v), on gradient mode. The LDs for the HPLC and LC–MS/MS methods, respectively, were 2.5 and 0.02 µg L?1, the LQs, 8.3 and 0.05 µg L?1, and the linear range from 10 up to 2000 µg L?1 and 0.05 up to 10 µg L?1. As expected, the LC–ESI–MS/MS–QTrap method was more sensitive and less laborious. The metabolite 4′‐hydroxy‐diclofenac was identified. Photolysis was used for the degradation studies and three products of diclofenac were identified (m/z of 214, 286 and 303) in aqueous solution. These results notwithstanding, no degradation products of diclofenac were found in the hospital effluent.  相似文献   

9.
Correct and precise age determination of prehistorical catastrophic rock‐slope failures prerequisites any hypotheses relating this type of mass wasting to past climatic regimes or palaeo‐seismic records. Despite good exposure, easy accessibility and a long tradition of absolute dating, the age of the 230 million m3 carbonate‐lithic Tschirgant rock avalanche event of the Eastern Alps (Austria) still is relatively poorly constrained. We herein review the age of mass‐wasting based on a total of 17 absolute ages produced with three different methods (14C, 36Cl, 234U/230Th). Chlorine‐36 (36Cl) cosmogenic surface exposure dating of five boulders of the rock avalanche deposit indicates a mean event age of 3.06 ± 0.62 ka. Uranium‐234/thorium‐230 (234U/230Th) dating of soda‐straw stalactites formed in microcaves beneath boulders indicate mean precipitation ages of three individual soda straws at 3.20 ± 0.26 ka, 3.04 ± 0.10 ka and 2.81 ± 0.15 ka; notwithstanding potential internal errors, these ages provide an ‘older‐than’ (ante quam) proxy for mass‐wasting. Based on radiocarbon ages (nine sites) only, it was previously suggested that the present rock avalanche deposit represents two successive failures (3.75 ± 0.19 ka bp , 3.15 ± 0.19 ka bp ). There is, however, no evidence for two events neither in surface outcrops nor in LiDAR derived imagery and drill logs. The temporal distribution of all absolute ages (14C, 36Cl, 234U/230Th) also does not necessarily indicate two successive events but suggest that a single catastrophic mass‐wasting took place between 3.4 and 2.4 ka bp . Taking into account the maximum age boundary given by reinterpreted radiocarbon datings and the minimum U/Th‐ages of calcite precipitations within the rock avalanche deposits, a most probable event age of 3.01 ± 0.10 ka bp can be proposed. Our results underscore the difficulty to accurately date catastrophic rock slope failures, but also the potential to increase the accuracy of age determination by combining methods. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   

10.
Environmental isotopes (2H or D, 18O, 3H), along with geology, hydrochemistry and in situ physicochemical parameters (EC, T, DO, pH) were employed to study surface water (reservoir, lake)–groundwater (spring) relationships at (1) Nagewadi, a minor irrigation project in the State of Maharashtra, Western India; (2) Kanhirapuzha reservoir in the State of Kerala, Southern India and (3) Ghatghar Pumped Storage Hydroelectric Project in the State of Maharashtra, Western India for the purpose of understanding the seepage/leakage and its associated problems. The studies concluded that the springs found downstream of the Nagewadi project originate from the reservoir and not from the abutments or shallow aquifers. The Kanhirapuzha reservoir receives a substantial base‐flow component compared to riverine inputs. The reason for the water‐logging problem at a nearby downstream village during the non‐summer periods is due to the change in the upstream groundwater flow direction under reservoir filling conditions and is not due to reservoir leakage. Most of the springs in the approach tunnel to the underground power house of the Ghatghar Project originate from the lower reservoir and not from the upper reservoir or the overburden rock matrix. The above case studies illustrate the diversity of environmental isotope applications in surface water (reservoir, lake)–groundwater (spring) relationships related to sustainability of hydro‐projects. Copyright © 2008 John Wiley & Sons, Ltd.  相似文献   

11.
The Hakusan volcano, central Japan, is located in a region where two subducting plates (the Pacific Plate and the Philippine Sea Plate) overlap near the junction of four plates adjacent to the Japanese Islands (the Pacific Plate, the Philippine Sea Plate, the Eurasia Plate, and the North American Plate). The Hakusan volcano consists of products from four major volcanic episodes: Kagamuro, Ko‐hakusan, and Shin‐Hakusan I and II. To date the eruption events of the Hakusan volcano we applied thermoluminescence and fission track methods. 238U(234U)–230Th disequilibrium and 206Pb/238U methods were applied to date the zircon crystallization ages for estimating the magma residence time before the eruptions. The eruption ages we obtained are ca 250 ka for Kagamuro, ca 100 ka and ca 60 ka for Ko‐Hakusan, ca 50 ka for Shin‐Hakusan I, and <10 ka for Shin‐Hakusan II. They are concordant with previous reports based on K–Ar dating. Some of the pyroclastic rocks, possibly originating from Shin‐Hakusan II activities, are dated to be ca 36 ka or 50 ka, and belong to the Shin‐Hakusan I activity. The zircon crystallization ages show several clusters prior to eruption. The magma residence time was estimated for each volcanic activity by comparing the major crystallization events and eruption ages, and we found a gradual decrease from ca. 500 ky for the Kagamuro activity to ca. 5 ky for the Shin‐Hakusan II activity. This decrease in residence time may be responsible for the decrease in volume of erupted material estimated from the current topography of the region. The scale of volcanic activity, which was deduced from the number of crystallized zircons, is more or less constant throughout the Hakusan volcanic activity. Therefore, the decrease in magma residence time is most likely the result of stress field change.  相似文献   

12.
Lead isotope data of sulfides and host volcanic rocks from the Bukit Botol and Bukit Ketaya deposits, the two representative deposits of the Tasik Chini volcanic‐hosted massive sulfide (VHMS) deposit, Central Belt of Peninsular Malaysia, are reported. Lead isotope compositions of the associated sulfide minerals and volcanic rocks from the Bukit Botol deposit exhibit homogeneous and less radiogenic values (206Pb/204Pb showing a range of composition from 18.14 to 18.20, 207Pb/204Pb between 15.52 and 15.59 and 208Pb/204Pb from 37.96 to 38.35). Similarly, the Pb isotopic compositions of the host volcanic rocks from the Bukit Ketaya deposit yielded a narrow range to those of the sulfide samples (206Pb/204Pb from 18.04 to 18.20, 207Pb/204Pb between 15.43 and 15.57 and 208Pb/204Pb of 37.96 to 38.30). The uniform Pb‐isotope compositions of the sulfides in the ore horizon and the host volcanic rocks from both deposits suggest a derivation from a similar source reservoir and mineralization processes. In the framework of the tectonic model for the Central Belt of Peninsular Malaysia, both deposits display a range of lead isotopic compositions originated from mixing of bulk crust/juvenile arc and minor mantle sources, which are typical for VHMS deposits in an island arc–back arc setting.  相似文献   

13.
There are wide spread Cenozoic volcanic rocks in Tengchong (CVRT), Yunnan province, SW China. These rocks comprise three rock types: basalt, andesite (dominant type) and dacite. Most samples are sub‐alkaline, and among the sub‐alkaline rocks, most are high‐K calc‐alkaline. These rocks have a SiO2 range of 49.1 wt.% to 66.9 wt.%. TiO2 contents are not high and have a variation of 0.7 wt.%–1.6 wt.%. Trace element concentrations and element ratios (such as Nb/U, Ce/Pb, Nb/La, etc.) of these rocks have a large variation. 87Sr/86Sr values fall in the range of 0.7057–0.7093 and 143Nd/144Nd values change from 0.5120 to 0.5125. 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios are in the range of 17.936–19.039, 15.614–15.810, and 38.894–39.735, respectively. These geochemical characteristics of CVRT make them resemble island‐arc volcanic rocks. We suggest that the magmas were generated in the lithospheric mantle that had already been metasomatized by previous subduction processes. By the study of the uplift history of the Tibetan Plateau, we found that the beginning of the geotectonic processes to the eruption of CVRT was coeval with one uplift event. Therefore, we propose that the uplift of the Tibetan Plateau caused collapse of the collisional orogeny in Tengchong, which further triggered the generation and eruption of the CVRT magmas.  相似文献   

14.
Comparative studies of the use of chlorine/ultraviolet (Cl2/UV) and hydrogen peroxide/ultraviolet (H2O2/UV) Advanced oxidation processes (AOPs) to remove trichloroethylene (TCE) from groundwater in a pump‐and‐treat application were conducted for the first time at the full‐scale operational level at two water treatment facilities in Northern California. In these studies, aqueous chlorine replaced hydrogen peroxide in the AOP treatment step, where the oxidant is exposed to UV light to produce highly reactive radical species that degrade groundwater contaminants. TCE removal rates as a function of initial chlorine dose and pH were then determined. At the site where the natural pH of the water was 7.1, TCE was removed (to a concentration of less than 0.5 µg/L) for nearly every chlorine dose point tested, and pH adjustment slightly enhanced the treatment process at this facility. The second site had a high natural pH of 7.7, and here, TCE was not completely removed for any chlorine dose up to 5.7 mg/L, although TCE removal did increase when the chlorine dose increased between 0.9 and 3.6 mg/L. Residual TCE remaining in the water post‐Cl2/UV was readily removed using active carbon filtration, which is part of the overall treatment train at this facility. These studies also verified that Cl2/UV AOP did not interfere with the photolysis of N‐nitrosodimethylamine or result in an effluent acutely toxic toward Ceriodaphnia dubia. Comparative economic analysis revealed that the chemical costs associated with Cl2/UV AOP were 25 to 50% of the costs associated with in place H2O2/UV AOP treatment.  相似文献   

15.
Abstract The Solund‐Stavfjord ophiolite complex (SSOC) in western Norway represents a remnant of the Late Ordovician oceanic lithosphere, which developed in an intermediate‐ to fast‐spreading Caledonian back‐arc basin. The internal architecture and magmatic features of its crustal component suggest that the SSOC has a complex, multistage sea floor spreading history in a supra‐subduction zone environment. The youngest crustal section associated with the propagating rift tectonics consists of a relatively complete ophiolite pseudostratigraphy, including basaltic volcanic rocks, a transition zone between the sheeted dyke complex and the extrusive sequence, sheeted dykes, and high‐level isotropic gabbros. Large‐scale variations in major and trace element distributions indicate significant remobilization far beyond that which would result from magmatic processes, as a result of the hydrothermal alteration of crustal rocks. Whereas K2O is strongly enriched in volcanic rocks of the extrusive sequence, Cu and Zn show the largest enrichment in the dyke complex near the dyke–volcanic transition zone or within this transition zone. The δ18O values of the whole‐rock samples show a general depletion structurally downwards in the ophiolite, with the largest and smallest variations observed in volcanic rocks and the transition zone, respectively. δ18O values of epidote–quartz mineral pairs indicate 260–290°C for volcanic rocks, 420°C for the transition zone, 280–345°C for the sheeted dyke complex and 290–475°C for the gabbros. The 87Sr/86Sr isotope ratios show the widest range and highest values in the extrusive rocks (0.70316–0.70495), and generally the lowest values and the narrowest range in the sheeted dyke complex (0.70338–0.70377). The minimum water/rock ratios calculated show the largest variations in volcanic rocks and gabbros (approximately 0–14), and generally the lowest values and range in the sheeted dyke complex (approximately 1–3). The δD values of epidote (?1 to ?12‰), together with the δ18O calculated for Ordovician seawater, are similar to those of present‐day seawater. Volcanic rocks experienced both cold and warm water circulation, resulting in the observed K2O‐enrichment and the largest scatter in the δ18O values. As a result of metal leaching in the hot reaction zone above a magma chamber, Zn is strongly depleted in the gabbros but enriched in the sheeted dyke complex because of precipitation from upwelling of discharged hydrothermal fluids. The present study demonstrates that the near intact effect of ocean floor hydrothermal activity is preserved in the upper part of the SSOC crust, despite the influence of regional lower greenschist facies metamorphism.  相似文献   

16.
Granular activated carbon (GAC) adsorption of two representative taste and odor (T & O) compounds, 2‐isopropyl‐3‐methoxy pyrazine (IPMP), and 2‐isobutyl‐3‐methoxy pyrazine (IBMP), in drinking water was investigated. Results show that the modified Freundlich equation best fit the experimental data during the adsorption isotherm tests, and the pseudo first‐order kinetics and intra‐particle diffusion kinetics well described the adsorption kinetics pattern. The calculated thermodynamic parameters (ΔH0, ΔS0, and ΔG0) indicated a spontaneous and endothermic adsorption process. Factors affecting the treatment efficiency were carefully evaluated. Acidic and alkaline conditions both favored GAC adsorption of IPMP and IBMP, especially the former. With the GAC dosage increasing, the first order adsorption rates increased, while the intra‐particle adsorption rates decreased. Within 12 h, 200 mg/L GAC could remove >90% of 150 µg/L IPMP and IBMP via adsorption at pH 3–11. Therefore, GAC is a promising treatment technology to control the T & O compounds associated water pollution.  相似文献   

17.
Rock fragment cover has long been an important agricultural crop production technique on the Loess Plateau, China. Although this approach plays an important role in controlling hydrological processes and preventing soil erosion, inconsistent results have been recovered in this field. In this study, we investigated the effects of rock fragment cover on infiltration, run‐off, soil erosion, and hydraulic parameters using rainfall simulation in the field in a semi‐arid region of China. Two field plots encompassing 6 rock fragment coverages (0%, 10%, 20%, 25%, 30%, and 40%), as well as 2 rock fragment positions and sizes were exposed to rainfall at a particular intensity (60 mm h?1). The results of this study showed that increasing the rock fragment coverage with rock fragments resting on the soil surface increased infiltration but decreased run‐off generation and sediment yield. A contrasting result was found, however, when rock fragments were partially embedded into the soil surface; in this case, a positive relationship between rock fragment coverage and run‐off rate as well as a nonmonotonic relationship with respect to soil loss rate was recovered. The size of rock fragments also exerted a positive effect on run‐off generation and sediment yield but had a negative effect on infiltration. At the same time, both mean flow velocity and Froude number decreased with increasing rock fragment coverage regardless of rock fragment position and size, whereas both Manning roughness and Darcy–Weisbach friction factor were positively correlated. Results show that stream power is the most sensitive hydraulic parameter affecting soil loss. Combined with variance analysis, we concluded that the order of significance of rock fragment cover variables was position followed by coverage and then size. We also quantitatively incorporated the effects of rock fragment cover on soil loss via the C and K factors in the Revised Universal Soil Loss Equation. Overall, this study will enable the development of more accurate modelling approaches and lead to a better understanding of hydrological processes under rock fragment cover conditions.  相似文献   

18.
Polyhydroxyalkanoates (PHAs), environmental friendly polyesters, can be produced by a wide range of microorganisms in nutrient‐limiting conditions. In the present study a new bacterial strain, able to produce high quantities of poly‐3‐hydroxybutyrate (PHB), is isolated from contaminated soil. The isolate is characterized and identified as Bacillus cereus Y23, based on morphological, physiological characteristics, and 16S ribosomal RNA gene sequences. PHB production is evaluated using different carbon and nitrogen sources and nutritional and culture conditions are optimized. The highest PHB production of 5.12 g L?1 was obtained in growth medium containing fructose and ammonium sulfate at a C/N ratio of 30, 0.3% yeast extract, 4.5 g L?1 phosphate solution, pH 7, inoculum size of 0.3%, and agitation rate of 150 rpm after 48 h of incubation at 32 °C. The PHB production decrement can be attributed to the intracellular utilization of the polymer during the stationary phase of the cellular growth and to the sporulation process. The presence of the main functional groups of PHB polymer is verified by Fourier‐transform infrared analysis. At optimum conditions, B. cereus Y23 turned out to be a good candidate for industrial production of PHB since it accumulates up to 67.9% of its dry weight.  相似文献   

19.
Fulvic acids of different origin, spray deposited on polished silicon after dissolution in high‐purity water without any additives, were analysed by time‐of‐flight secondary ion mass spectrometry (TOF‐SIMS) in combination with oblique 24...36 keV SF5+ ion bombardment. The observed, highly reproducible mass spectra cover more than five orders of magnitude in dynamic range, without background subtraction. Apart from lines due to atomic ions and low‐mass ion fragments, the mass spectra exhibit broad maxima between m/z 200...350, mainly due to a beat‐like superposition of lines at every single mass number, up to at least m/z 400. In the negative ion spectra the beats have a spacing of m/z 14, corresponding to a CH2‐unit. The high‐mass tails of the spectra extend well beyond m/z 5000, with similar slopes in the positive and the negative ion mass spectra. The negative spectra appear to be less affected by fragmentation products than the positive spectra. Fulvic acids (FAs) of different origin show distinctly different spectra, with mean masses ranging between m/z ≈ 450 and 580 (for a low‐mass cut‐off m/z 150). To further verify the ability of TOF‐SIMS to detect molecules and clusters with masses significantly above the maxima of the FA spectra, samples of glycyrrhizic acid (GA, as GA ammonium salt with molecular weight 840) were also analysed. Parent ions as well as multimers (GA)n were observed as positive and negative ions, up to n = 4 (m/z 3320). The results are compared with spectra recently obtained by other mass spectrometric techniques.  相似文献   

20.
Phosphorus (P) export from agricultural lands above known threshold levels can result in adverse impacts to receiving water quality. Phosphorus loss occurs in dissolved and sediment‐bound, or particulate phosphorous (PP), forms, with the latter often dominating losses from row‐cropped systems. To target practices, land managers need good computer models and model developers need good monitoring data. Sediment monitoring data (e.g. radiometric finger printing and sediment P sorption capacity) can help identify sediment source areas and improve models, but require more sediment mass than is typically obtained by automatic sampling. This study compares a simple suspended sediment sampler developed at the University of Exeter (UE) with automatic sampling in intermittent channels draining corn and alfalfa fields. The corn field had a greater runoff coefficient (27%) than alfalfa (11%). No differences were found in enrichment ratios (sediment constituent/soil constituent) in PP (PPER) or percent loss on ignition (LOIER) between paired UE samplers on corn. The median LOIER for the UE samplers (1·9%) did not differ significantly (p > 0·13) from the automatic sampler (2·0%). The PPER from the UE samplers was on average 20% lower than the automatic samplers. A correlation (r2 = 0·75) was found between sediment PP and % LOI from automatic samplers and UE samplers for particles < 50 µm, while for > 50 µm PP concentration did not change with changes in % LOI. Sediment ammonium‐oxalate extractable metals were similarly related to LOI, with the strongest correlation for iron (r2 = 0·71) and magnesium (r2 = 0·70). Copyright © 2011 John Wiley & Sons, Ltd.  相似文献   

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