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1.
Apatite distributions and compositions from cumulates from the EPR at Hess Deep, the MAR at the Kane Transform, and the SWIR at ODP Hole 735B were determined to assess the variability at each setting and to evaluate the potential utility of apatite in understanding the evolution of the lower ocean crust. Apatite in cumulates with low P2O5 contents are heterogeneously distributed along linear arrays or in tight clusters suggesting they crystallized from planar or pipe-like channels of evolved liquid. Most of the variation in the apatite composition is in the halogen site. The XApF and XApCl are inversely correlated defining trends at near constant XApOH with EPR XApOH=0.25, MAR XApOH=0.45, and SWIR XApOH=0.65. These trends are defined both by sample averages and by the range of individual analyses in samples with large ranges in their F/Cl ratio. These trends are interpreted to reflect the reequilibration of apatite from variably evolved liquids/fluids that moved through the crystal mush. Comparison of the F–Cl–OH contents of apatite with the F–Cl–OH contents of glasses recovered from the same ridges show approximate correspondence: apatite and glasses from the EPR have the highest halogen contents while apatite and glasses from the MAR and SWIR have more OH. Some of the higher Cl contents in the apatite are interpreted to be produced by degassing of the cumulus pile while others reflect the assimilation of a seawater component. We suggest that systematic analysis of apatite from oceanic cumulates might allow cumulates that crystallized at shallow depths and assimilated seawater-derived components to be distinguished from those that crystallized below the level of seawater interaction.  相似文献   

2.
29Si,27Al MAS NMR and IR spectra of rnonophase K-feldspars (sanidine, orthoclase and microcline) and Na-feldspars (monalbite, anorthoclase and low albite) in different structural states have been studied. The NMR and IR spectra of K-feldspars and Na-feldspars vary regularly along with their degrees of Si/Al ordering evolution. Si in orthoclase occupiesT 2m,T2o andT1m, and the high-temperature Na-feldspar (monalbite and anorthoclase) coincides in29Si,27Al NMR and IR spectra. Moreover, all the high-temperature Na-feldspars and sanidine have the same27Al NMR and IR spectra. Project supported by the Foundation of Laboratory of Magnetic Resonance and Atom and Molecular Physics, Wuhan Institute of Physics, Chinese Academy of Sciences.  相似文献   

3.
Precipitation of Aluminium and Phosphate Affected by Acidification Acidified waters often show elevated concentrations of Al (with up to 6 mg L–1 being not unusual). A pH increase resulting e.g. from mixing with non‐acidified water or from biological activities may be linked with Al precipitation. Up to now, this phenomenon was described for acid mine drainages. This investigation focuses on a whitish precipitate naturally formed in a brook of an atmospherically acidified catchment in the Ore Mountains, Germany. Based on infrared spectra the precipitate was identified as an Al‐hydroxosulfate with crystal water. A simulation of natural conditions in the laboratory showed that Al precipitated only if sulfate or phosphate ions were added to the solution. In the case of sulfate being added, the infrared spectrum of the precipitate was similar to the natural precipitate. 27Al NMR spectroscopy revealed tetrahedrally coordinated Al in some precipitates which evidences the participation of the tridecameric [Al13O4(OH)24(H2O)12]7+ cation beside other polymeric Al cations. Precipitation experiments subjected to the given conditions showed that the phosphate elimination from solution with Al was much higher than with Fe. With Al and Fe added together, the P elimination rate was likewise high, and phosphate was bound onto Al in the precipitate. This was demonstrated by SEM‐EDX spectroscopy. Based on these results we present a possible reaction mechanism. The precipitation of Al together with P allows a significant retention of both elements in sediments because in contrast to Fe, Al immobilizes phosphate even under anoxic conditions.  相似文献   

4.
The study area is located in the east part of the Trans-Mexican Volcanic Belt, in the Las Cumbres Volcanic Complex (LCVC) which lies between two large stratovolcanoes: Pico de Orizaba (5700 m a.s.l.) to the south, and Cofre de Perote (4200 m a.s.l.) to the NNE. The most conspicuous structure of the LCVC is a 4-km-diameter circular crater with a dacitic dome in the center, which constitutes the remains of a destroyed stratovolcano.The Quetzalapa Pumice (QP) was produced by a plinian eruption that was dated by the 14C method at 20 000 yr. BP. The eruptive sequence consists predominantly of pumice fall deposits and scarce intra-plinian pyroclastic flow deposits, which crop out on the west flank of the LCVC. The absence of post-plinian ignimbrite deposits is striking.The deposits are well sorted, clast-supported with reverse grading at the base, with a medium to high accessory lithics content. The maximum average thickness of the deposit in the proximal areas is about 15 m and has been divided into three members: the Basal Member (BM), 2 m thick with four submembers (BMf1, BMf2, BMf3, and BMafl), the Intermediate Member (IM), 10 m thick with two submembers (IMpf and IMaf), and the Upper Member (UM), 3 m thick with four submembers (UMpl, UMsdf, UMwaf, and UMpls).The predominant component of the fall deposits is a white, highly vesiculated pumice with 71% SiO2 content. Plagioclase is the most abundant mineral followed by 1–3-mm-long biotite phenocrysts. The accessory lithics are lavas mostly of andesitic composition. Their abundance increases toward the uppermost levels of the sequence.We calculate a minimum volume of 8.4 km3 (2.22 km3 dense rock equivalent), for the entire QP deposit. Isopach and isopleth maps show that the IM deposit has an elongated distribution with a NNE–SSW direction, whereas the UM deposit has a circular distribution.We estimate a maximum eruptive column height for the IM of 20 km. Field studies and isopach and isopleth maps indicate that the eruptive column was affected by a strong wind.Previous studies located the QP source in the Las Cumbres crater. However, based on the isopach and isopleth distribution, and the lack of pumice fall deposits inside the Las Cumbres crater, we consider that the QP emission center is located on the west flank of the LCVC, and was buried by its own pumice fall deposits. It coincides with an explosion crater called La Capilla formed during the closing phase of the QP eruption.A ‘pumice fountain’ model is proposed to explain the observed sequence of deposits. According to this model, the material was emitted through a ‘hose-type’ conduit during a monogenetic eruption of rhyolitic composition. This kind of volcanic activity is not extensively reported in the literature.  相似文献   

5.
The present study focuses on the morphotectonic evolution of the axial portion of the Southern Apennine chain between the lower Calore River valley and the northern Camposauro mountain front (Campania Region). A multidisciplinary approach was used, including geomorphological, field‐geology, stratigraphical, morphotectonic, structural, 40Ar/39Ar and tephrostratigraphical data. Results indicate that, from the Lower Pleistocene onwards, this sector of the chain was affected by extensional tectonics responsible for the onset of the sedimentation of Quaternary fluvial, alluvial fan and slope deposits. Fault systems are mainly composed of NW‐SE, NE–SW and W‐E trending strike‐slip and normal faults, associated to NW‐SE and NE–SW oriented extensions. Fault scarps, stratigraphical and structural data and morphotectonic indicators suggest that these faults affected the wide piedmont area of the northern Camposauro mountain front in the Lower Pleistocene–Upper Pleistocene time span. Faults affected both the oldest Quaternary slope deposits (Laiano Synthem, Lower Pleistocene) and the overlying alluvial fan system deposits constrained between the late Middle Pleistocene and the Holocene. The latter are geomorphologically and chrono‐stratigraphically grouped into four generations, I generation: late Middle Pleistocene–early Upper Pleistocene, with tephra layers 40Ar/39Ar dated to 158±6 and 113±7 ka; II generation: Upper Pleistocene, with tephra layers correlated with the Campanian Ignimbrite (39 ka) and with the slightly older Campi Flegrei activity (40Ar/39Ar age 48±7 ka); III generation: late Upper Pleistocene–Lower Holocene, with tephra layers correlated with the Neapolitan Yellow Tuff (~15 ka); IV generation: Holocene in age. The evolution of the first three generations was controlled by Middle Pleistocene extensional tectonics, while Holocene fans do not show evidence of tectonic activity. Nevertheless, considering the moderate to high magnitude historical seismicity of the study area, we cannot rule out that some of the recognized faults may still be active. Copyright © 2018 John Wiley & Sons, Ltd.  相似文献   

6.
Hu  AnPing  Li  Jian  Zhang  WenZheng  Li  ZhiSheng  Hou  Lu  Liu  QuanYou 《中国科学:地球科学(英文版)》2008,51(1):183-194

The Ordos Basin, the second largest sedimentary basin in China, contains the broad distribution of natural gas types. So far, several giant gas fields have been discovered in the Upper and Lower Paleozoic in this basin, each having over 1000×108m3 of proven gas reserves, and several gas pools have also been discovered in the Mesozoic. This paper collected the data of natural gases and elucidated the geochemical characteristics of gases from different reservoirs, and then discussed their origin. For hydrocarbons preserved in the Upper Paleozoic, the elevated δ 13C values of methane, ethane and propane indicate that the gases would be mainly coal-formed gases; the singular reversal in the stable carbon isotopes of gaseous alkanes suggests the mixed gases from humic sources with different maturity. In the Lower Paleozoic, the δ 13C1 values are mostly similar with those in the Upper Paleozoic, but the δ 13C2 and δ 13C3 values are slightly lighter, suggesting that the gases would be mixing of coal-type gases as a main member and oil-type gases. There are multiple reversals in carbon isotopes for gaseous alkanes, especially abnormal reversal for methane and ethane (i.e. δ 13C1>δ 13C2), inferring that gases would be mixed between high-mature coal-formed gases and oil-type gases. In the Mesozoic, the δ 13C values for gaseous alkanes are enriched in 12C, indicating that the gases are mainly derived from sapropelic sources; the carbon isotopic reversal for propane and butane in the Mesozoic is caused by microbial oxidation and mixing of gases from sapropelic sources with different maturity. In contrast to the Upper Paleozoic gases, the Mesozoic gases are characterized by heavier carbon isotopes of iso-butane than normal butane, which may be caused by gases generated from different kerogen types. Finally, according to δ 13C1-R 0 relationship and extremely low total organic carbon contents, the Low Paleozoic gases would not be generated from the Ordovician source as a main gas source, bycontrast, the Upper Paleozoic source as a main gas source is contributed to the Lower Paleozoic gases.

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7.
Ocean-floor basalts and glasses were recovered from three stations along the western Nazca plate, from a sublinear topographic feature believed to represent the proto-East Pacific Rise (EPR), and include abyssal tholeiites, FeTi-basalts and glasses, as well as transitional and little fractionated compositions. When compared with their coexisting fresh glasses, the FeTi-basalts have higher total alkalies, TiO2 and MgO, and lower FeO*, suggesting that they have also been affected by non-oxidative post-magmatic alteration processes. The FeTi-glasses form a remarkably uniform compositional group through space and time. A little fractionated composition having anMg-number= 73, similar to those reported from the Mathematician Ridge, has higher Na2O and TiO2, and slightly lower CaO than similar compositions from the slowly accreting Mid-Atlantic Ridge. The basalts and glasses reported here exhibit the compositional diversity expected for propagating rifts and probably represent more than one volcanic episode.Both geochemical and geophysical interpretations support the inference that the EPR grew from Miocene times by the progressive growth and propagation of mantle perturbations, leaving a remnant sublinear zone of rough topography characteristic of slower accretion as the trace of the proto-EPR. Continuing translations and rotations of axial segments are occurring along the EPR, probably in response to self-reorganizations of mantle flow patterns arising from rapid melting and depletion of the source regions. The data allow the inference that the youthful rift systems of the eastern Pacific are far from thermodynamic equilibrium as might be expected if such systems were to drive fundamental life processes.  相似文献   

8.
The Ordos Basin, the second largest sedimentary basin in China, contains the broad distribution of natural gas types. So far, several giant gas fields have been discovered in the Upper and Lower Paleozoic in this basin, each having over 1000×108m3 of proven gas reserves, and several gas pools have also been discovered in the Mesozoic. This paper collected the data of natural gases and elucidated the geochemical characteristics of gases from different reservoirs, and then discussed their origin. For hydrocarbons preserved in the Upper Paleozoic, the elevated δ 13C values of methane, ethane and propane indicate that the gases would be mainly coal-formed gases; the singular reversal in the stable carbon isotopes of gaseous alkanes suggests the mixed gases from humic sources with different maturity. In the Lower Paleozoic, the δ 13C1 values are mostly similar with those in the Upper Paleozoic, but the δ 13C2 and δ 13C3 values are slightly lighter, suggesting that the gases would be mixing of coal-type gases as a main member and oil-type gases. There are multiple reversals in carbon isotopes for gaseous alkanes, especially abnormal reversal for methane and ethane (i.e. δ 13C1>δ 13C2), inferring that gases would be mixed between high-mature coal-formed gases and oil-type gases. In the Mesozoic, the δ 13C values for gaseous alkanes are enriched in 12C, indicating that the gases are mainly derived from sapropelic sources; the carbon isotopic reversal for propane and butane in the Mesozoic is caused by microbial oxidation and mixing of gases from sapropelic sources with different maturity. In contrast to the Upper Paleozoic gases, the Mesozoic gases are characterized by heavier carbon isotopes of iso-butane than normal butane, which may be caused by gases generated from different kerogen types. Finally, according to δ 13C1-R 0 relationship and extremely low total organic carbon contents, the Low Paleozoic gases would not be generated from the Ordovician source as a main gas source, bycontrast, the Upper Paleozoic source as a main gas source is contributed to the Lower Paleozoic gases.  相似文献   

9.
In order to identify the distribution of aluminium (Al) within an acid hillslope and its release to a stream, the spatial distribution of acid ammonium oxalate extractable Al (Alo) and exchangeable Al3+ have been investigated on a podzolized hillslope in Bicknoller Combe, Somerset, UK. The eluviated Al from topsoils is mainly deposited in the lower soil horizons forming podzolic B horizons, but some Al flows downslope carried by lateral throughflow. Al oxides may provide the main source of exchangeable Al3+ on the study slope due to high soil acidity. Examination of the spatial distribution of exchangeable Al3+ suggests that the slope hollow, where active convergent throughflow occurs, and the saturation wedge at the base of the slope are the main delivery routes of dissolved Al3+ to the stream. Divalent base cations (Ca2+ and Mg2+), supplied from atmospheric input and organic decomposition and carried by throughflow, exchange Al3+ via cation exchange reactions under high water content. Laterally illuviated Al oxides in the lower hollow adjacent to the saturation wedge probably provide a pool for continuous delivery of Al either as soluble or complexed forms to the stream via the saturated wedge. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

10.
The Monte Nuovo eruption is the most recent event that occurred at Phlegrean Fields (Italy) and lasted from 29 September to 6 October 1538. It was characterized by 2 days of quasi-sustained phreatomagmatic activity generating pumice-bearing pyroclastic density currents and forming a 130-m-high tuff cone (Lower Member deposits). The activity resumed after a pause of 2 days with two discrete Vulcanian explosions that emplaced radially distributed, scoria-bearing pyroclastic flows (Upper Member deposits). The juvenile products of Lower and Upper Members are, respectively, phenocryst-poor, light-coloured pumice and dark scoria fragments with K-phonolitic bulk compositions, identical in terms of both major and trace elements. Groundmass is formed by variable proportions of K-feldspar and glass, along with minor sodalite and Fe-Ti oxide present in the most crystallized samples. Investigations of groundmass compositions and textures were performed to assess the mechanisms of magma ascent, degassing and fragmentation along the conduit and implications for the eruptive dynamics. In pumice of the Lower Member groundmass crystal content increases from 13 to 28 vol% from the base to the top of the sequence. Products of the Upper Member consist of clasts with a groundmass crystal content between 30 and 40 vol% and of totally crystallized fragments. Crystal size distributions of groundmass feldspars shift from a single population at the base of the Lower Member to a double population in the remaining part of the sequence. The average size of both populations regularly increases from the Lower to the Upper Member. Crystal number density increases by two orders of magnitude from the Lower to the Upper Member, suggesting that nucleation dominated during the second phase of the eruption. The overall morphological, compositional and textural data suggest that the juvenile components of the Monte Nuovo eruption are likely to record variations of the magma properties within the conduit. The different textures of pumice clasts from the Lower Member possibly reflect horizontal gradients of the physical properties (P, T) of the ascending magma column, while scoriae from the second phase are thought to result from the disruption of a slowly rising plug crystallizing in response to degassing. In particular, crystal size distribution data point to syn-eruptive degassing-induced crystallization as responsible for the transition in eruptive style from the first to the second phase of the eruption. This mechanism not only has been proved to profoundly affect the dynamics of dome-forming calc-alkaline eruptions, but may also have a strong influence in driving the eruption dynamics of alkaline magmas of intermediate to evolved compositions.Editorial responsibility: J. Donnelly-Nolan  相似文献   

11.
Aromatic hydrocarbons are generally main distillation of crude oil and organic extract of source rocks. Bicyclic and tricyclic aromatic hydrocarbons can be purified by two-step method of chromatography on alumina. Carbon isotopic composition of individual aromatic hydrocarbons is affected not only by thermal maturity, but also by organic matter input, depositional environment, and hydrocarbon generation process based on the GC-IRMS analysis of Upper Ordovician, Lower Ordovician, and Cambrian source rocks in different areas in the Tarim Basin, western China. The subgroups of aromatic hydrocarbons as well as individual aromatic compound, such as 1-MP, 9-MP, and 2,6-DMP from Cambrian-Lower Ordovician section show more depleted 13 C distribution. The 13 C value difference between Cambrian-Lower Ordovician section and Upper Ordovician source rocks is up to 16.1‰ for subgroups and 14‰ for individual compounds. It can provide strong evidence for oil source correlation by combing the 13 C value and biomarker distribution of different oil and source rocks from different strata in the Tarim Basin. Most oils from Tazhong area have geochemical characteristics such as more negative 13C9-MP value, poor gammacerane, and abundant homohopanes, which indicate that Upper Ordovician source rock is the main source rock. In contrast, oils from Tadong area and some oils from Tazhong area have geochemical characteristics such as high 13C9-MP value, abundant gammacerane, and poor homohopanes, which suggest that the major contributor is Cambrian-Lower Ordovician source rock.  相似文献   

12.
Concentrations of both aluminium (Al) and dissolved organic carbon (DOC) in stream waters are likely to be regulated by factors that influence water flowpaths and residence times, and by the nature of the soil horizons through which waters flow. In order to investigate landscape‐scale spatial patterns in streamwater Al and DOC, we sampled seven streams draining the Hubbard Brook valley in central New Hampshire. We observed considerable variation in stream chemistry both within and between headwater watersheds. Across the valley, concentrations of total monomeric aluminium (Alm) ranged from below detection limits (<0·7 µmol l−1) to 22·3 µmol l−1. In general, concentrations of Alm decreased as pH increased downslope. There was a strong relationship between organic monomeric aluminium (Alo) and DOC concentrations (R2 = 0·92). We observed the highest Alm concentrations in: (i) a watershed characterized by a steep narrow drainage basin and shallow soils and (ii) a watershed characterized by exceptionally deep forest floor soils and high concentrations of DOC. Forest floor depth and drainage area together explained much of the variation in ln Alm (R2 = 0·79; N = 45) and ln DOC (R2 = 0·87; N = 45). Linear regression models were moderately successful in predicting ln Alm and ln DOC in streams that were not included in model building. However, when back‐transformed, predicted DOC concentrations were as much as 72% adrift from observed DOC concentrations and Alm concentrations were up to 51% off. This geographic approach to modelling Al and DOC is useful for general prediction, but for more detailed predictions, process‐level biogeochemical models are required. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

13.
The organic composition and organic‐inorganic interaction in paper mill sludge (PS) solvent extracts (hexane, ethyl acetate, acetone and ethanol) and humic fractions, humic acid (HA) and humin (HU) were studied by electron paramagnetic resonance spectroscopy (EPR), proton and carbon‐13 nuclear magnetic resonance spectroscopy (1H NMR; 13C NMR), Fourier‐transformed infrared spectroscopy (FTIR), and ultraviolet‐visible spectroscopy (UV‐vis). The strategy of fractionating the PS, sequentially, with organic solvents of increasing polarity is a reliable analytical procedure for humic substance sample separation because it results in more purified fractions. FTIR, 1H NMR and 13C NMR results showed that hexane extract consisted mainly of aliphatic hydrocarbon structures. Their contents in the extracts decreased as the polarity of the extracting solvent increased and the content of oxygen functional groups increased. Carboxylic and carboxylate functional groups were found in the acetone extract, and ester and ether functions were predominantly found in the ethanol extract. EPR spectra revealed some Fe3+ complexes with rhombic structure (g1 = 4.3; g2 = 9.0) in the humic fractions and in all solvent extracts, except hexane. Quasi‐octahedral Fe3+ complexes (g = 2.3; ΔHpp ≤ 400 G) were found in the HU fraction and in the acetone extract. The organic free radical content in the HA fraction was higher than the non‐fractionated PS sample and HU fraction.  相似文献   

14.
Infrared and X-ray radiation data indicate that the effect of pressure on Na-Al-Si-O quenched melt is to change the coordination number of trivalent aluminum ions from four to six. This conclusion is based upon an observed decrease in the intensity of the infrared vibration involving a “bridging” oxygen in the polymer structure and a shift in both Al Kα (7 × 10?4Å) and Al Kβ (20 × 10?4Å) radiation. The amount of AlIV or AlVI seems to be a continuous function of the pressure at which the melt was formed and is thus independent of the coordination change effected at high pressure in solids crystallized from the NaAlSi2O6 composition used in this study. The importance of the continuous shift of coordination number of aluminum ions in silicate melts at high pressure is discussed. The change in coordination of Al would also be expected in natural silicate melts (magmas) at high pressures.  相似文献   

15.
Cosmogenic isotope burial dating, using 10Be and 26Al, was applied to Plio–Pleistocene fluvial successions from the Lower Rhine Embayment, Germany. The approach consists of three principal steps: (1) measurement of cosmogenic nuclides in depth profiles, (2) modelling of hypothetical nuclide concentrations based on a first-order conceptualisation of the geological context and the principal succession of depositions and subsequent erosional and burial phases, and (3) using parameter estimation to identify values for the a priori unknown model parameters (burial age, initial nuclide concentrations, terrace erosion rates) that result in minimal disagreement between hypothetical and measured nuclide concentrations.The Late Pliocene Kieseloolite Formation was dated to 3650 ± 1490 ka and the Early Pleistocene Waalre Formation to 900 ± 280 ka. The unconformably overlying Upper Terrace Formation revealed ages of 740 ± 210 ka and 750 ± 250 ka for the two different sites. These findings are in good agreement with independent age control derived by bio-, magneto-, and litho-stratigraphy. Furthermore, identifiability and uncertainty analysis reveal a relationship between burial depth and sensitivity of isotope concentrations to burial age and erosion rate. Our results indicate that using shallower buried samples would enable a considerably more robust estimation of the burial age and the terrace erosion rate. Uncertainties arose mainly from nuclide measurements, and not from the uncertainties derived from modelling or insufficient knowledge of nuclide production and decay properties.  相似文献   

16.
Humic acid plays an important role in the distribution of heavy metals in the environment. The aims of this study were conducted to evaluate the spectroscopic characteristics and aluminum (Al) adsorption of humic acids which were extracted from four composts. The functional groups were determined by Fourier transform infrared spectroscopy (FTIR) and solid‐state 13C nuclear magnetic resonance spectroscopy (13C‐NMR). The results showed that the aromatic groups were all found in the humic acids of the four composts, and the surface of humic acids included carboxylic group, hydroxylic group, and amino group. The experiment of Al adsorption was described by Freundlich equation. It showed that the adsorption of Al by humic acid from compost of cattle manure was higher, but that from the compost of pig manure, lemon manure, tea manure in equal preparation was lower. The adsorptive behavior was different due to the interaction by functional groups ( OH and  COOH) with Al. These results can describe the fate and transportation of Al in the soil of different organic fertilizer.  相似文献   

17.
Crucian carp were exposed to three combinations of pH and inorganic aluminium concentrations for 25 days. Mortality, plasma chloride and haematocrit, and gill aluminium content were investigated. No mortality was observed in any of the three exposures. Crucian carp survived acidic Al-rich water (pH 5.17) with a high concentration of low-molecular weight inorganic Al species (242 µgl–1) for 25 days. These fish had lowered plasma chloride levels and high amounts of aluminium on their gills compared to fish exposed to acidic Al-poor water (pH 5.16 and 12 µgl–1 Ali) and control water (pH 6.29 and 4 µgl–1 Ali). Haematocrit was the same in all three exposures. Because aluminium was not acutely toxic to the anoxia tolerant crucian carp, the present results give support to the hypothesis that Al polymerization with subsequent hypoxia is of high importance for the mechanism of acute Al toxicity to fish.  相似文献   

18.
A series of polyaluminum chloride sulfate (PACS) coagulants, which have different SO42–/Al3+ and OH/Al (γ) mole ratio, has been successfully developed using AlCl3·6H2O, Al2(SO4)3·18H2O and Na2CO3 as raw materials. The coagulation performance of PACS for removing natural organic matter (NOM) from surface water was evaluated, and the effect of SO42–/Al3+ mole ratio and γ value in coagulants PACS on DOC and UV254 removal was determined. Furthermore, the influence of pH and dosage of the selected PACS with a SO42–/Al3+ ratio of 0.0664 and a γ value of 2.0, which achieved the best coagulation performance for the removal of DOC and UV254 of all PACS coagulants, on the removal of DOC and UV254 and residual aluminum concentration in treated water was investigated. The results were compared with the ones of polyaluminum chloride (PAC) with γ value of 2.0. The experimental data show that the performance of PACS as a coagulant was highly dependent on SO42–/Al3+ mole ratio and γ value. Both for the selected PACS and for PAC, the best DOC and UV254 removal results were obtained in the range of pH from 5.0 to 8.2 and at the coagulation dose of 5.0 mg/L as Al. Under the optimum coagulation conditions, the selected PACS gave higher DOC and UV254 removal efficiencies, and lower residual aluminum concentrations in the treated water than PAC. The maximum removal of DOC and UV254 for PACS was approximately 88.0% and 93.0%, respectively. At the optimum coagulant dose and pH 6.5, the concentration of residual aluminum in treated water by both selected PACS and PAC can comply with the regulated limits. The major mechanisms of NOM removal by PACS and PAC coagulation involve complexation‐charge‐neutralization‐precipitation.  相似文献   

19.
The oxygen isotope composition of fossil roots that have been permineralized by hematite are presented from eight different stratigraphic levels spanning the Upper Pennsylvanian and Lower Permian strata of north-central Texas. Hematite δ18O values range from − 0.4% to 3.7%. The most negative δ18O values occur in the upper Pennsylvanian strata, and there is a progressive trend toward more positive δ18O values upward through the lower Permian strata. This stratigraphic pattern is similar in magnitude and style to δ18O values reported for penecontemporaneous authigenic palaeosol phyllosilicates and calcites, suggesting that all three minerals record similar paragenetic histories that are probably attributed to temporal palaeoenvironmental changes across the Late Pennsylvanian and Early Permian landscapes.Palaeotemperature estimates based on paired δ18O values between penecontemporaneous hematite and phyllosilicate samples suggest these minerals co-precipitated at relatively low temperatures that are consistent with a supergene origin in a low-latitude soil-forming environment. Hematite–phyllosilicate δ18O pairs indicate (1) relatively low soil temperatures (∼ 24 ± 3 °C) during deposition of the upper Pennsylvanian strata followed by (2) a considerable rise in soil temperatures (∼ 35–37 ± 3 °C) during deposition of the lowermost Permian strata. Significantly, δD and δ18O values of contemporaneous phyllosilicates provide single mineral palaeotemperature estimates that are analytically indistinguishable from temperature estimates based on hematite–phyllosilicate oxygen isotope pairs. The results between the two temperature-proxy methods suggest that the inferred large temperature change across the Upper Pennsylvanian–Lower Permian boundary might be taken seriously. If real, such a significant climate change would have undoubtedly had far-reaching ecological effects within this region of Pangaea. Notably, there are important lithological and palaeobotanical changes, such as disappearance of coal and coal swamp floras, across the Upper Pennsylvanian–Early Permian boundary of north-central Texas that may be consistent with major climatic change toward warmer conditions.  相似文献   

20.
Our understanding of the ancient ocean-atmosphere system has focused on oceanic proxies. However, the study of terrestrial proxies is equally necessary to constrain our understanding of ancient climates and linkages between the terrestrial and oceanic carbon reservoirs. We have analyzed carbon-isotope ratios from fossil plant material through the Valanginian and Lower Hauterivian from a shallow-marine, ammonite-constrained succession in the Crimean Peninsula of the southern Ukraine in order to determine if the Upper Valanginian positive carbon-isotope excursion is expressed in the atmosphere. δ13Cplant values fluctuate around − 23‰ to − 22‰ for the Valanginian-Hauterivian, except during the Upper Valanginian where δ13Cplant values record a positive excursion to ∼− 18‰. Based upon ammonite biostratigraphy from Crimea, and in conjunction with a composite Tethyan marine δ13Ccarb curve, several conclusions can be drawn: (1) the δ13Cplant record indicates that the atmospheric carbon reservoir was affected; (2) the defined ammonite correlations between Europe and Crimea are synchronous; and (3) a change in photosynthetic carbon-isotope fractionation, caused by a decrease in atmospheric pCO2, occurred during the Upper Valanginian positive δ13C excursion. Our new data, combined with other paleoenvironmental and paleoclimatic information, indicate that the Upper Valanginian was a cool period (icehouse) and highlights that the Cretaceous period was interrupted by periods of cooling and was not an equable climate as previously thought.  相似文献   

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