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1.
Temporal changes in paleoproductivity of Lake Biwa (Japan) over the past 32 kyr have been studied by analyzing bulk organic carbon and photosynthetic pigments (chlorins) in the BIW95-5 core. Primary productivity was estimated on the assumption of C/Norg values of 8 for autochthonous organic matter (OM) and 25 for allochthonous OM and using an equation developed for the marine environment. The estimate indicates that primary productivity ranges from 50 to 90 g C m?2 yr?1 in the Holocene, while it is ～60 g C m?2 yr?1 on average in the last glacial. Pheophytin a and pheophorbide a are the major chlorins. A downcore profile of chlorin concentration normalized to autochthonous organic carbon (OC) shows a decreasing trend. Chlorin productivity was corrected by removal of the effect of post-burial chlorin degradation. The temporal profile of chlorin productivity thereby obtained resembles that from autochthonous OC.The difference in primary productivity between the Holocene and the glacial for the lake is markedly smaller than that for Lake Baikal situated in the boreal zone. This difference between the two lakes is probably caused by the difference in their climatic conditions, such as temperature and precipitation. Precipitation at Lake Biwa is relatively large during the glacial and the Holocene because of the continuous influence of the East Asian monsoon. Lake Baikal precipitation is generally small as a result of control by the continental (Siberia) climate regime. In addition, a significant difference in productivity between the glacial and the Holocene for Lake Baikal may be essentially controlled by the hydrodynamic systems in the lake.Lake Biwa terrigenous OM input events occurred at least five times over the period 11–32 kyr BP, suggesting enhanced monsoon activity. Molecular examination of the layer with a large input of terrigenous OM during the Younger Dryas indicates that concentrations of terrigenous biomarkers such as n-C27–C31 alkanes, lignin phenols, cutin acids, ω-hydroxy acids and C29 sterols are high, suggesting that soil OM with peat-like material entered the lake as a result of flooding. An enhanced sedimentation rate in the last 3000 years might have been partially caused by agricultural activity around the lake.  相似文献   

2.
Emission of phosphine, a gaseous form of P, is presently considered a potential pathway of the P biogeochemical cycle in aquatic sediments. This study investigated the emission fluxes of phosphine and its potential production mechanisms in the intertidal marshes of the Yangtze Estuary. It is shown that the relatively high emission fluxes of phosphine were measured in warm seasons, with the values of 3.85–24.9 ng m?2 h?1 and 4.21–36.5 ng m?2 h?1 in August and September, respectively. In contrast, lower fluxes of phosphine appeared in May (1.23–6.32 ng m?2 h?1) and January (0.21–0.91 ng m?2 h?1). Also, the fluxes of phosphine were generally higher in the freshwater marsh, compared with the brackish marsh. The spatio-temporal pattern of phosphine emissions was observed to be mainly associated with sediment structure, temperature and salinity. Meanwhile, the significant correlations of phosphine emissions with sedimentary P and alkaline phosphatase activities reflect that phosphine probably derives from the microbial transformations of PO4 and organic P. In addition, it is estimated that approximately 1.08 × 106 g of phosphine is released annually from sediments into the pelagic water of the Yangtze Estuary. Therefore, it is concluded that phosphine emissions may be an important internal source of P, making a significant contribution to the occurrence of algal blooms especially during warm seasons.  相似文献   

3.
《Quaternary Science Reviews》2005,24(10-11):1217-1222
Tide gauge data at seven sites of the Permanent Service for Mean Sea Level (PSMSL), with information for relative sea-level during the past 140–200 yr, were analyzed to examine the rates and causes of the global sea-level rise (GSLR) during the twentieth century. By subtracting linear trends for relative sea-level rise during the past 100 yr from the observed data, we get the apparent GSLRs of ∼1 mm yr−1 for five sites around the Baltic Sea and Brest. The rate for San Francisco is significantly larger than this, with an optimum value ∼2 mm yr−1. The spatial difference of ∼1 mm yr−1 between these sites is reasonably explained by the recent melting of the Greenland ice sheet with an equivalent sea-level rise of ∼1 mm yr−1. The predicted relative sea-level change for this melting scenario is 0.5 mm yr−1 at sites around the Baltic Sea and Brest, and 1.5 mm yr−1 for San Francisco. The residuals between observations and predictions, ∼0.5 mm yr−1 at all sites, may be contributed by thermal expansion of seawater and/or other melting sources. These results suggest the rate of twentieth-century GSLR to be 1.5 mm yr−1.  相似文献   

4.
Glaciers erode bedrock but are also efficient conveyors of debris supplied during a cycle of glaciation by processes other than basal erosion. In this dual capacity as both an eroding and a transporting agent lies the ambiguity of ‘glacial erosion’ as a geomorphic process, with implications for methods of measuring the removal of rock mass by glaciers in the geological past, and for interpreting what exactly the consequences have been on topography and elevation change. A global review of ～400 Quaternary glacial denudation rates estimated from five different measurement techniques provides values ranging between 10?4 and 10 mm yr?1. We investigate the causes of such wide variability by examining the respective influences of environmental setting and methodological bias. A reference frame chosen for assessing these issues is the Massif du Carlit (Pyrenees, France), where a quantified mass balance of the well preserved glacial, periglacial and paraglacial deposits was made possible by detailed geomorphological mapping and terrestrial cosmogenic nuclide dating of extant erosional and depositional landform sequences. Resulting age brackets helped to define three main episodes of ice-cap growth and decline, each characterized by a volume of debris and a mappable source area. Erosion rates were expressed in two ways: (i) as spatially averaged denudation rates (D) during the successive stages of glacial advance to the line of maximum ice extent (MIE), post-MIE ice recession, and Lateglacial cirque readvance, respectively; and (ii) as cirque-wall recession rates (R) where moraine facies criteria indicated a supraglacial provenance of debris. Results indicate low erosion (D ≈ 0.05 mm yr?1) during the ice advance phase, probably because of thin or passive ice covering the low-gradient subglacial topography that occurs just above the late Pleistocene equilibrium line altitude (2.2–2.4 km). Erosion rates peaked (D ≈ 0.6 mm yr?1 and R ≈ 2.4–4.5 mm yr?1) during the main transition to ice-free conditions, when deglacial debuttressing promoted the rapid response of freshly exposed slope systems to new equilibrium conditions in the steep crest zone. Lateglacial D- and R-values declined to 0.2–0.3 mm yr?1, with indications of spatially variable R controlled by lithology. In this environment glaciers overall behaved more as conveyors of debris supplied by supraglacial rock exposures in the mountain crest zone than as powerful modifiers of subglacial topography. This explains the widespread preservation of deep, in situ preglacial weathering profiles on relict Cenozoic land surfaces in the deglacierized part of the Eastern Pyrenees. When plotted on the global data set analyzed and discussed in the review, the East Pyrenean erosion rates stand out as being amongst the lowest on record.  相似文献   

5.
Among the various methods used to determine vertical water seepage in unsaturated soils, thermal convection presents significant advantages: temperature measurements are simple to perform and record, and a wide range of time scales can be considered. The authors analysed the data recorded by the meteorological stations of the Seine river basin, at three different depths: 20, 50 and 100 cm. As the measurement sensitivity was limited to 0.1 K, long series of data needed to be stacked in order to obtain sufficient precision to quantify the convective component of heat transfer, in a predominantly conductive context. For the period from 1984 to 2001, it was possible to determine the average recharge at each station, and the recharge variation between groups of three-year periods. By interpolating these data over the whole basin, a global assessment has been made and compared to the exported flow rate at the river mouth: the resulting value of 94 mm yr?1 lies between the lowest annual rate, 52 mm yr?1, and the mean total exported value of 252 mm yr?1.  相似文献   

6.
《Quaternary Science Reviews》2005,24(12-13):1391-1411
Temporal and spatial changes in glacier cover throughout the Late Quaternary in Tibet and the bordering mountains are poorly defined because of the inaccessibility and vastness of the region, and the lack of numerical dating. To help reconstruct the timing and extent of glaciation throughout Tibet and the bordering mountains, we use geomorphic mapping and 10Be cosmogenic radionuclide (CRN) surface dating in study areas in southeastern (Gonga Shan), southern (Karola Pass) and central (Western Nyainqentanggulha Shan and Tanggula Shan) Tibet, and we compare these with recently determined numerical chronologies in other parts of the plateau and its borderlands. Each of the study regions receives its precipitation mainly during the south Asian summer monsoon when it falls as snow at high altitudes. Gonga Shan receives the most precipitation (>2000 mm a−1) while, near the margins of monsoon influence, the Karola Pass receives moderate amounts of precipitation (500–600 mm a−1) and, in the interior of the plateau, little precipitation falls on the western Nyainqentanggulha Shan (∼300 mm a−1) and the Tanggula Shan (400–700 mm a−1). The higher precipitation values for the Tanggula Shan are due to strong orographic effects. In each region, at least three sets of moraines and associated landforms are preserved, providing evidence for multiple glaciations. The 10Be CRN surface exposure dating shows that the formation of moraines in Gonga Shan occurred during the early–mid Holocene, Neoglacial and Little Ice Age, on the Karola Pass during the Lateglacial, Early Holocene and Neoglacial, in the Nyainqentanggulha Shan date during the early part of the last glacial cycle, global Last Glacial Maximum and Lateglacial, and on the Tanggula Shan during the penultimate glacial cycle and the early part of the last glacial cycle. The oldest moraine succession in each of these regions varies from the early Holocene (Gonga Shan), Lateglacial (Karola Pass), early Last Glacial (western Nyainqentanggulha Shan), and penultimate glacial cycle (Tanggula Shan). We believe that the regional patterns and timing of glaciation reflect temporal and spatial variability in the south Asian monsoon and, in particular, in regional precipitation gradients. In zones of greater aridity, the extent of glaciation has become increasingly restricted throughout the Late Quaternary leading to the preservation of old (≫100 ka) glacial landforms. In contrast, in regions that are very strongly influenced by the monsoon (≫1600 mm a−1), the preservation potential of pre-Lateglacial moraine successions is generally extremely poor. This is possibly because Lateglacial and Holocene glacial advances may have been more extensive than early glaciations and hence may have destroyed any landform or sedimentary evidence of earlier glaciations. Furthermore, the intense denudation, mainly by fluvial and mass movement processes, which characterize these wetter environments, results in rapid erosion and re-sedimentation of glacial and associated landforms, which also contributes to their poor preservation potential.  相似文献   

7.
《Gondwana Research》2014,25(3-4):969-983
The Ediacaran–Cambrian Petermann Orogeny, central Australia, is an exceptional example of intraplate orogenesis. It involved sub-eclogite facies metamorphism and extreme basin inversion during the exhumation of Musgrave Province basement from beneath the formerly contiguous Centralian Superbasin. Sensitive High Resolution Ion Microprobe (SHRIMP) U–Pb geochronology of zircon, titanite and rutile, along with Ti-in-zircon thermometry from meta-igneous samples, have been used to determine the timing and duration of high-pressure metamorphism and subsequent cooling associated with this orogenic event. Peak metamorphic temperatures of 720–760 °C were attained at 544 ± 7 Ma (U–Pb zircon). Subsequent cooling to 600–660 °C by ~ 521 Ma occurred at a rate of ~ 2.6–7.0 °C Myr− 1, as recorded by the closure of Pb diffusion in titanite. Further cooling to 585–560 °C by 498–472 Ma occurred at a rate of 0.9–4.8 °C Myr− 1, as recorded by Pb closure in rutile. The duration of tectonism was long-lived (> 40 Myr) across the central and western parts of the orogenic system, and deformation occurred in a comparatively warm and weak portion of crust, characterised by regional thermal gradients of 17–26 °C km− 1. This proposed duration of tectonism is much longer than that permitted by a shear heating mechanism, which requires an exceptionally short duration of tectonism, and additionally, an overall cold lithosphere characterised by geothermal gradients of ~ 9 °C km− 1.  相似文献   

8.
The solubility of synthetic ZnS(cr) was measured at 25–250 °C and P = 150 bars as a function of pH in aqueous sulfide solutions (~ 0.015–0.15 m of total reduced sulfur). The solubility determinations were performed using a Ti flow-through hydrothermal reactor. The solubility of ZnS(cr) was found to increase slowly with temperature over the whole pH range from 2 to ~ 10. The values of the Zn–S–HS complex stability constant, β, were determined for Zn(HS)20(aq), Zn(HS)3?, Zn(HS)42?, and ZnS(HS)?. Based on the experimental values the Ryzhenko–Bryzgalin electrostatic model parameters for these stability constants were calculated, and the ZnS(cr) solubility and the speciation of Zn in sulfide-containing hydrothermal solutions were evaluated. The most pronounced solubility increase, about 3 log units at m(Stotal) = 0.1 for the temperatures from 25 to 250 °C, was found in acidic solutions (pH ~ 3 to 4) in the Zn(HS)20(aq) predominance field. In weakly alkaline solutions, where Zn(HS)3? and Zn(HS)42? are the dominant Zn–S–HS complexes, the ZnS(cr) solubility increases by 1 log unit at the same conditions. It was found that ZnS(HS)? and especially Zn(HS)42? become less important in high temperature solutions. At 25 °C and m(Stotal) = 0.1, these species dominate Zn speciation at pH > 7. At 100 °C and m(Stotal) = 0.1, the maximum fraction of Zn(HS)42? is only 20% of the total Zn concentration (i.e. at pHt ~ 7.5), whereas at 350 °C and 3 <pHt <10, the fraction of Zn(HS)42? and ZnS(HS)? is less than 0.05% and 2.5% respectively, of the total Zn concentration and Zn(HS)20 and Zn(HS)3? predominate. The measured equilibrium formation constants were combined with the literature data on the stability of Zn–Cl complexes in order to evaluate the concentration and speciation of Zn in chloride solutions. It was found that at acidic pH, and in more saline fluids having total chloride > 0.05 m, Zn–Cl complexes are responsible for hydrothermal Zn transport with no significant contribution of Zn–S–HS complexes. The hydrosulfide/sulfide complexes will play a more important role in lower salinity (< 0.05 m chloride) hydrothermal solutions which are characteristic of many epithermal ore depositing environments. The value of ΔfG° (β-ZnS(cr)) = ? 198.6 ± 0.2 kJ/mol at 25 °C was determined via solubility measurements of natural low-iron Santander (Spain) sphalerite.  相似文献   

9.
Increased seismicity and occurrences of hot springs having surface temperature of 36–58 °C are observed in the central part of India (74–81° E, 20–25° N), where the NE trending Middle Proterozoic Aravalli Mobile Belt meets the ENE trending Satpura Mobile Belt. Earlier Deep Seismic Sounding (DSS) studies along Thuadara-Sendhwa-Sindad profile in the area has showed Mesozoic Sediments up to around 4 km depth covered by Deccan Trap and the Moho depth with a boundary velocity (Pn) of 8.2 km/s. In the present study, surface heat flow of 48 ± 4 mW m?2 has been estimated based on Pn velocity, which agrees with the value of heat flow of 52 ± 4 mW m?2 based on Curie point isotherms estimates. The calculated temperature-depth profile shows temperature of 80–120 °C at the basement, which is equivalent to oil window temperature in Mesozoic sediments and around 570–635 °C at Moho depth of 38–43 km and the thermal lithosphere is about 110 km thick, which is comparatively higher than those of adjoining regions. The present study reveals the brittle–ductile transition zone at 14–41 km depth (temperature around 250–600 °C) where earthquake nucleation takes place.  相似文献   

10.
Although oil cracking has been documented as one of the important sources of gas in many overmature marine sedimentary basins, the chemical and carbon isotopic signatures of gases of this origin are still open to question. In this study a Cambrian crude oil from the central Tarim basin, along with its main separated fractions (saturates, aromatics and asphaltenes), were pyrolyzed in sealed gold tubes to investigate how generated gases vary in chemical and carbon isotopic composition and how this variation would influence the genetic interpretation of oil cracking gas. The results indicate that the gases from cracking of aromatics and asphaltenes are much drier and more enriched in 13C than the gases from the cracking of saturates and crude oil at the same level of thermal maturity. In the experimental run of 20 °C/h, the dryness index of the gases (defined as the volume percentage of C1 in C1–5) from the cracking of saturates ranges from 26.2–90.6% with the methane carbon isotope change ranging from −54.8‰ to −35.5‰, whereas the dryness index is never lower than 60.6% for the gases from the cracking of aromatics with methane carbon isotope ranging from −39.9‰ to −32.2‰. Correspondingly, experimental data for the four samples plot in different areas in diagrams designed to distinguish oil cracking gas from kerogen cracking gas, such as ln(C2/C3) vs. δ13C2–δ13C3 and δ13C1 vs. δ13C2–δ13C3, indicating compositional variability of crude oil could assert an important influence in these diagrams. Therefore it is prudent to bring other geological constraints into consideration to avoid misinterpretation.The kinetic parameters for the bulk generation of C1–5 gas and the methane carbon isotope fractionation extrapolated to geological conditions of 2 °C/Ma and an initial temperature of 50 °C show that the temperatures of C1–5 gas generation from the aromatics and asphaltenes are lower than those from the saturates and crude oil due to their lower activation energies and frequency factors. Generation of C1–5 gases from the aromatics is modeled to be initiated about 122 °C whereas the initiation temperature for the saturates sample is 176 °C. Below 189 °C (EasyRo = 1.8%), the yields of C1–5 gases follow the order: aromatics > asphaltenes > crude oil > saturates. At similar thermal maturity levels, the methane carbon isotopic compositions are significantly different for the four samples, with an order of 13C enrichment: aromatics > asphaltenes > crude oil > saturates, however the difference in methane carbon isotopes becomes smaller with increasing temperature. This indicates that methane carbon isotopic values can be significantly different for gases cracked from oils that are compositionally diverse, especially in the early stage of methane generation.  相似文献   

11.
In EGS projects, fault zones are considered as the structures controlling deep flow at the reservoir scale. Using a large set of petrophysical properties (porosity, density, permeability, thermal conductivity [TC]) measured on cores collected along the EPS-1 borehole, a model of fault zone is proposed to describe them. A fault zone is a complex structure, showing different parts with different kinds of deformations and/or materials that could explain chemical and physical processes observed during fluid-rock interactions. The different parts composing the fault zone are: (1) the fault core or gauge zone; (2) the damage zone; (3) and the protolith. They are usually heterogeneous and show different physical properties. The damage zone is a potential high permeability channel and could become the main pathway for fluids if secondary minerals seal the fault core. Porosity is the lowest within the protolith, between 0.5 and 1%, but can go up to 15% in the fault zone. Permeability ranges from 10?20 m2 in the fresh granite to, at least, 10?15 m2 in the fault core, and TC ranges from 2.5 W K?1m?1 to 3.7 W K?1m?1. Finally, variations in specific surface are set over two orders of magnitude. If the lowest values usually characterize the fresh granite far from fault zones, physical properties could show variations spread over their whole respective ranges within these fault zones.  相似文献   

12.
《Quaternary Science Reviews》2003,22(10-13):1207-1211
The time-integrated slip rate in fault zones can be determined if the deformed deposits are reliably dated. Here, we report optically stimulated luminescence (OSL) ages of Late Pleistocene fluvial deposits cut by the Wangsan fault, southeastern Korea, which displaces a hanging wall block of about 28 m. Five sandy samples of the deformed Quaternary deposits were dated by quartz OSL using the single aliquot regenerative-dose (SAR) protocol. Three samples taken from the footwall block show stratigraphically consistent OSL ages of 54±7, 76±5 and 90±6 ka, from top to bottom. Two samples collected from the same layer in the hanging wall block show reproducible OSL ages of 81±5 and 82±5 ka, which are also in good agreement with the stratigraphic relationships. Our OSL ages yield an average sedimentation rate of the Quaternary deposits as around 0.04 mm a−1, and a minimum value of time-integrated slip rate as 0.52 mm a−1. This minimum slip rate is considerably higher than those reported earlier for Quaternary faults in southeastern Korea. The youngest OSL age (54±7 ka) constrains the maximum value of the recurrence interval of the fault movement.  相似文献   

13.
The oxidation of surface functional groups on biochar increases its reactivity and may contribute to the cation exchange capacity of soil. In this study, two Eucalyptus wood biochars, produced at 450 °C (B450) and 550 °C (B550), were incubated separately in each of the four contrasting soils for up to 2 years at 20 °C, 40 °C and 60 °C. Carbon functional groups of the light fraction (< 1.8 g/cm3) of the control and biochar amended soils (fresh and aged for 1 and 2 years at 20 °C, 40 °C and 60 °C) were investigated using near-edge X-ray absorption fine structure (NEXAFS) spectroscopy and X-ray photoelectron spectroscopy (XPS). The spectra of biochar and light fractions of the control and biochar amended soils showed two distinct peaks at ∼285.1 eV and 288.5 eV, which were attributed to the C1s-π1CC transitions of aromatic C and C1s-π1CO transitions of carboxylic C, carboxyamide C and carbonyl C. The proportion of aromatic C was substantially greater in the light fraction of the biochar amended soils than the corresponding light fraction of the control soils. Also, the proportion of aromatic C was much higher in the light fraction of the B550 amended soils than in the corresponding B450 amended soils. Neither NEXAFS nor XPS results show any consistent change in the proportion of aromatic C of biochar amended soils after 1 year ageing. However, XPS analysis of hand-picked biochar samples showed an increase in the proportion of carboxyl groups after ageing for 2 years, with an average value of 8.9% in the 2 year aged samples compared with 3.0% in the original biochar and 6.4% in the control soil. Our data suggest that much longer ageing time will be needed for the development of a significant amount of carboxyl groups on biochar surfaces.  相似文献   

14.
The kinetics of forward extraction [AuCl4]? from aqua regia medium by diethylene glycol dibutyl ether (DBC) have been investigated by the Lewis cell (LC) technique. At first gold extraction has been carried out under different experimental conditions for achieving the stoichiometry coefficients and the value of the extraction equilibrium constant (K = 0.1). For kinetic data treatment, flux ‘F’ method has been applied. Reaction order with respect to DBC, pH and [AuCl4]? was determined and then the rate constant was calculated. The rate of gold extraction from 2 M chloride medium can be expressed as F = 100.88[AuCl4?]1.25 [DBC]0.4 [H+]?0.22. Kinetics data were treated by EVIEWS software and coefficients were obtained. The comparison of manual and software results indicated that the results had good conformity. Influence of temperature was studied and then activation energy, Ea, (11.17 kJ/mol), activation enthalpy (11.66 kJ/mol) and entropy (?187 J/mol K) were calculated by using Arrhenius and activation complex theory respectively. Ea value (< 20.9 kJ/mol) indicates that, the extraction of gold (III) in the investigated system is controlled by diffusion process.  相似文献   

15.
Previously studied thermosequences of wood (chestnut) and grass (rice straw) biochar were subjected to hydrogen pyrolysis (hypy) to evaluate the efficacy of the technique for determining pyrogenic carbon (CP) abundance. As expected, biochar from both wood and grass produced at higher temperature had higher CP amount. However, the trend was not linear, but more sigmoidal. CP/CT ratio values (CT = total organic carbon) for the wood thermosequence were ⩽0.03 at biochar production temperature (TCHAR) ⩽ 300 °C. They increased dramatically until 600 °C and remained relatively constant and near unity at higher biochar production temperature. Grass biochar was similar in profile, but CP/CT values rose dramatically after 400 °C. The findings are consistent with the hypothesis that hypy residues contain polycyclic aromatic hydrocarbons (PAHs) with a degree of condensation above at least 7–14 fused rings, with labile organic matter and pyrogenic PAHs below this degree of condensation removed by hypy.Both wood and grass thermosequences displayed δ13CP values that decreased with increased TCHAR, indicating that recalcitrant carbon compounds (pyrogenic aromatic PAHs with a relatively high degree of condensation) were first formed from structural components with relatively high δ13C values (e.g. cellulose). Relatively constant δ13C values at TCHAR ⩾ 500 °C suggested the dominant pyrolysis reaction was condensation of PAHs with no additional fractionation. Comparison of hypy with benzene polycarboxylic acid (BPCA), ‘ring current’ NMR and pyrolysis gas chromatography–mass spectrometry (GC–MS) results from the same suite of samples indicated a consistent overview of the structure of CP, but provided unique and complimentary information.  相似文献   

16.
The interior thermal regime of a field-scale experimental waste rock pile in the Northwest Territories, Canada, was studied. Test pile construction was completed in the summer 2006, and temperature data was collected continuously since that time to February 2009. The temperature data indicates the test pile cooled over the study period, with an average heat energy release of −2.5 × 104 and −2.6 × 104 MJ in 2007 and 2008, respectively. The mean annual air temperature (MAAT) at the site was −8.9 °C during the period between 2006 and 2009, with a permafrost table at a depth of 4 m in bedrock away from the pile. Because of this cold environment, the upward movement rate of the 0 °C isotherm into the test pile at its base was approximately 1.5 m a−1 during 2007 and 2008. Thermistor strings installed immediately below the base of the test pile showed the test-pile basal temperatures remained near and below 0 °C during the study period. Furthermore, due to low rates of sulfide mineral oxidation, elevated temperatures in the interior of the test pile were not observed. The average air velocity in the pore space in July 2007 and 2008 was about one third of that during January of each year based on temperature distributions. Therefore, due to higher air velocity during the winter, it is expected that heat transfer is greater during winter.  相似文献   

17.
Three models were examined to predict C aromaticity (fa) of biochars based on either their elemental composition (C, H, N and O) or fixed C (FC) content. Values of fa from solid state 13C nuclear magnetic resonance (NMR) analysis with Bloch-decay (BD) or direct polarisation (DP) techniques, concentrations of total C, H, N, and organic O, and contents of FC of 60 biochars were either compiled from the literature (dataset 1, n = 52) or generated in this study (dataset 2, n = 8). Models were first calibrated with dataset 1 and then validated with dataset 2. All models were able to fit dataset 1 when atomic H to C ratio (H/C) < 1 (except two ash rich biochars) and to estimate fa of HF treated biochars (H/C < 1). Model 1, which was based on values of H/C only and calibrated with a root mean square of error (RMSE) of 0.04 fa-unit (n = 41), could predict the experimental data with a RMSE = 0.02 fa-unit (n = 6). Model 2, which was based on biochar elemental composition data, showed the most accurate prediction, with a RMSE of 0.03 fa-unit (n = 41) for the calibration data, and of 0.02 fa-unit (n = 6, H/C < 1) for the validation data. Model 3, which was based on contents of FC and C, and modified with a correction factor of 0.96, displayed the highest RMSE (0.06 fa-unit, n = 19) among the three models. Models 1 and 2 did not work properly for samples having either an H/C ratio > 1, high concentrations of carbonate or high inorganic H. These models need to be further tested with a wider range of biochars before they can be recommended for classification of biochar stability.  相似文献   

18.
Physical, physicochemical, and mineralogical-petrographic methods have been applied to samples of ophiolite-hosted chromite ore from different deposits and occurrences in the Urals. Temperature dependences of dielectric loss obtained for nine chromite ore samples consisting of 95–98% Cr spinel show prominent peaks indicating a relaxation origin of the loss. The analyzed samples have the loss peaks at different temperatures depending mainly on H = (FeO/Fe2O3)? : (FeO/Fe2O3)??, where (FeO/Fe2O3)? and (FeO/Fe2O3)?? are, respectively, the ferrous/ferric oxide ratios in the samples before and after heating to 800 °C, and H is thus the heating-induced relative change in the FeO/Fe2O3 ratio. These peak temperatures vary from 550 °C (sample 1, high-Cr chromium spinel with more than 52% Cr2O3) to 750 °C (sample 2, aluminous and magnesian spinel with less than 30% Cr2O3), and H ranges correspondingly from 1.61 to 5.49. The temperature of the loss peaks is related with H as H = 34.30 ? 11.52N + 1.20N2, with an error of σ = 0.19 (N = T · 10?2, T is temperature in °C).  相似文献   

19.
Uranium(VI) sorption onto kaolinite was investigated as a function of pH (3–12), sorbate/sorbent ratio (1 × 10?6–1 × 10?4 M U(VI) with 2 g/L kaolinite), ionic strength (0.001–0.1 M NaNO3), and pCO2 (0–5%) in the presence or absence of 1 × 10?2–1 × 10?4 M citric acid, 1 × 10?2–1 × 10?4 M EDTA, and 10 or 20 mg/L fulvic acid. Control experiments without-solids, containing 1 × 10?6–1 × 10?4 M U(VI) in 0.01 M NaNO3 were used to evaluate sorption to the container wall and precipitation of U phases as a function of pH. Control experiments demonstrate significant loss (up to 100%) of U from solution. Although some loss, particularly in 1 × 10?5 and 1 × 10?4 M U experiments, is expected due to precipitation of schoepite, adsorption on the container walls is significant, particularly in 1 × 10?6 M U experiments. In the absence of ligands, U(VI) sorption on kaolinite increases from pH ～3 to 7 and decreases from pH ～7.5 to 12. Increasing ionic strength from 0.001 to 0.1 M produces only a slight decrease in U(VI) sorption at pH < 7, whereas 10% pCO2 greatly diminishes U(VI) sorption between pH ～5.5 and 11. Addition of fulvic acid produces a small increase in U(VI) sorption at pH < 5; in contrast, between pH 5 and 10 fulvic acid, citric acid, and EDTA all decrease U(VI) sorption. This suggests that fulvic acid enhances U(VI) sorption slightly via formation of ternary ligand bridges at low pH, whereas EDTA and citric acid do not form ternary surface complexes with the U(VI), and that all three ligands, as well as carbonate, form aqueous uranyl complexes that keep U(VI) in solution at higher pH.  相似文献   

20.
Multiple proxies from a 319-cm peat core collected from the Hudson Bay Lowlands, northern Ontario, Canada were analyzed to determine how carbon accumulation has varied as a function of paleohydrology and paleoclimate. Testate amoeba assemblages, analysis of peat composition and humification, and a pollen record from a nearby lake suggest that isostatic rebound and climate may have influenced peatland growth and carbon dynamics over the past 6700 cal yr BP. Long-term apparent rates of carbon accumulation ranged between 8.1 and 36.7 g C m? 2 yr? 1 (average = 18.9 g C m? 2 yr? 1). The highest carbon accumulation estimates were recorded prior to 5400 cal yr BP when a fen existed at this site, however following the fen-to-bog transition carbon accumulation stabilized. Carbon accumulation remained relatively constant through the Neoglacial period after 2400 cal yr BP when pollen-based paleoclimate reconstructions from a nearby lake (McAndrews et al., 1982) and reconstructions of the depth to the water table derived from testate amoeba data suggest a wetter climate. More carbon accumulated per unit time between 1000 and 600 cal yr BP, coinciding in part with the Medieval Climate Anomaly.  相似文献   

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