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1.
The methylation index (MBT or MBT′) of branched glycerol dialkyl glycerol tetraethers (brGDGTs) in soils along altitudinal transects of some mountains, e.g. Mount (Mt.) Shennongjia and Mt. Gongga, exhibited no correlation with altitude or mean annual air temperature (MAT) alone. However, a significant correlation between MBT′, cyclization ratio (CBT) of brGDGTs and MAT for each transect could still be found. To investigate the reason, we reanalyzed the brGDGTs in soils from Mt. Shennongjia using an improved liquid chromatography method and examined whether the newly described 6-methyl brGDGTs were the main cause of the large scatter in the correlation between MBT′ and MAT. In contrast to MBT′, the MBT′5ME, based on 5-methyl brGDGTs alone, correlated significantly with MAT (R2 0.89, p < 0.001) but had no relationship with soil pH. However, MBT′6ME, based only on 6-methyl brGDGTs, was strongly dependent on soil pH. This suggests that pH dependent 6-methyl brGDGTs introduce large scatter in the correlation between MBT′ and MAT, which is likely to mechanistically explain the poor relationship between MBT′ and MAT, yet good correlation between MBT′, pH and MAT. A series of indices derived from 6-methyl brGDGTs, including IRIIIa′ and IRIIa′ (isomer ratio of structures IIIa′ and IIa′, respectively), correlated with soil pH and can be used as new paleo pH indicators to supplement the classic CBT proxy. The tetramethylated brGDGTs with 0–1 cyclopentyl rings (Ia and Ib) were found to comprise unknown isomers, whose abundances also appear to increase with soil pH. A further optimized liquid chromatography method is needed to quantify these new isomers more accurately and to determine the environmental controls on them.  相似文献   

2.
The combined application of plant wax δD (δDwax) and branched glycerol dialkyl glycerol tetraethers (brGDGTs) has been suggested as proxy for paleo-elevation. In some of the altitudinal transects studied so far, nonlinear precipitation gradients, large variations in seasonality, soil and vegetation types introduced substantial amounts of scatter in the relationship between these proxies and altitude. To further evaluate the principal functioning of the proxies, δDwax and brGDGTs were analysed in surface soils along an altitude gradient (from 28 m up to 1865 m a.s.l.) in Meghalaya, India. The transect experiences limited seasonal temperature variation and receives very high monsoonal precipitation along the whole elevation gradient. The δDwax show a significant relation with altitude (r2 = 0.72). The additional fits with stream water δD (r2 = 0.72) and modelled precipitation δD (r2 = 0.72) indicate that δDwax tracks the altitude effect on precipitation. Also the brGDGT distribution shows a correlation with altitude, reflecting the decrease in temperature with higher elevation (r2 = 0.65, or r2 = 0.66 using the original and recalibrated methylation of branched tetraethers-cyclisation of branched tetraethers (MBT–CBT) proxy). Application of the original MBT–CBT calibration generates calculated air temperatures that overestimate measured air temperature by ∼6 °C, whereas temperatures similar to measured are obtained with the revised calibration. These results indicate that δDwax and brGDGTs may faithfully and accurately track environmental changes with altitude for transects where seasonal and diurnal temperature variability is relatively limited. Furthermore, proxy application to locations that experience high rainfall increases the suitability as climatic indicators, as it excludes soil moisture availability as a limiting factor.  相似文献   

3.
Glycerol dialkyl glycerol tetraethers (GDGTs) and bulk organic geochemical parameters were examined for a short core from the Bohai Sea, a Yellow River-dominated continental margin. A three end member mixing model using branched/isoprenoid tetraethers (BIT) index, δ13C and C/N shows that the average fractions of soil, marine and plant organic matter (OM) during the period of 1933–2011 are 67.7% (38–92%), 26.1% (0–58%) and 6.2% (0–23%), respectively. Abrupt changes of sedimentary OM compositions around 1953, 1976 and 1996 are synchronous with the Yellow River mouth relocations. The BIT index values (0.33–0.80) present a stronger correlation with crenarchaeol abundance (R2 = 0.88) than branched GDGTs abundance (R2 = 0.27), suggesting that variations of marine Thaumarchaeota abundance rather than soil OM inputs is the first order factor controlling the BIT index values, although this proxy has been widely used for soil OM. The comparison between the BIT index, nutrient status and historical Yellow River sediment load indicates that the high sensitivity of the BIT index to the Yellow River channel shifts cannot be explained by a nutrient stimulation mechanism, but instead is likely caused by the restriction of Thaumarchaeota growth in highly turbid water due to the enormous sediment inputs from Yellow River. Our study demonstrates that local conditions should be considered when applying the BIT index as an environmental proxy.  相似文献   

4.
The distribution of glycerol dialkyl glycerol tetraethers (GDGTs) can reflect continental environmental changes. Recently, the distribution of branched GDGTs (bGDGTs) has been proposed as a novel tool for paleoelevation reconstructions. Here we report the variation in TEX86 (tetraether index of 86 carbon atoms) of isoprenoidal GDGTs (iGDGTs) and MBT (methylation of branched tetraether index) of bGDGTs along an altitudinal transect on Mt. Xiangpi, NE Qinghai-Tibetan Plateau. Both TEX86 and MBT values of surface soils showed significant linear decreases with altitude (TEX86: R2 = 0.65; n = 50; MBT: R2 = 0.69; n = 24). We suggest that the apparent relationships between the two indices and altitude may be related to temperature. Our preliminary investigation suggests that the TEX86 index can potentially be applied as a paleoelevation indicator in addition to the MBT index on the Qinghai-Tibetan Plateau.  相似文献   

5.
Branched glycerol dialkyl glycerol tetraethers (GDGTs) are membrane lipids of unknown bacteria that are ubiquitous in soil and peat. Two indices based on the distribution of these lipids in soils, the Cyclization of Branched Tetraethers (CBT) and the Methylation of Branched Tetraethers (MBT) indices have been shown to correlate with soil pH, and mean annual air temperature (MAT) and soil pH, respectively, and can be used to reconstruct MAT in palaeoenvironments. To verify the extent to which branched GDGTs in marine sediments reflect the distribution pattern on land and whether these proxies are applicable for palaeoclimate reconstruction in high latitude environments with a MAT of <0 °C, we compared the branched GDGT distribution in Svalbard soils and nearby fjord sediments. Although branched GDGT concentrations in the soil are relatively low (0.02–0.95 μg/g dry weight (dw)) because of the cold climate and the short growing season, reconstructed MATs based on the MBT/CBT proxy are ca. ?4 °C, close to the measured MAT (ca. ?6 °C). Concentrations of branched GDGTs (0.01–0.20 μg/g dw) in fjord sediments increased towards the open ocean and the distribution was strikingly different from that in soil, i.e. dominated by GDGTs with one cyclopentane moiety. This resulted in MBT/CBT-reconstructed MAT values of 11–19 °C, well above measured MAT. The results suggest that at least part of the branched GDGTs in marine sediments in settings with a low soil organic matter (OM) input may be produced in situ. In these cases, the application of the MBT/CBT palaeothermometer will generate unrealistic MAT reconstructions. The MBT/CBT proxy should therefore only be used at sites with a substantial input of soil OM relative to the amount of marine OM, i.e. at sites close to the mouth of rivers with a catchment area where sufficient soil formation takes place and the soil thus contains substantial amounts of branched GDGTs.  相似文献   

6.
The relative abundances and distributions of branched glycerol dialkyl glycerol tetraethers (brGDGTs) in marine and lacustrine sediments have been recently used as paleo-environmental proxies for the input of soil organic matter and past continental temperatures, respectively. The putative main source of brGDGTs is soil bacteria. Therefore, these biomarkers are also part of the soil organic matter stock that accumulates in the terrigenous environment. Here we present a method for isolating and purifying these compounds from lake sediments, soils and peat for radiocarbon (14C) measurement using a combination of normal and reversed phase high performance liquid chromatography, allowing complete separation of co-eluting compounds. Radiocarbon analysis was performed on an accelerator mass spectrometer system equipped with a gas ion source. We assessed the accuracy and the necessary corrections with modern and radiocarbon-dead procedural blanks. Blank assessment revealed that the reverse phase step introduced significant amounts of extraneous carbon, while the normal phase step did not. We show that with our method and instrumentation it is possible to obtain accurate and precise 14C analyses of brGDGTs with sample amounts as small as 10 μg C. Finally we demonstrate the application of the measurement of 14C concentrations of several brGDGTs isolated from lake sediments and peat soils.  相似文献   

7.
Isoprenoid and branched glycerol dialkanol diethers (iso GDDs and br GDDs) have recently been detected in various environments, including sediment, soil and peat deposits. Their structures strongly resemble those of glycerol dialkyl glycerol tetraethers (GDGTs). Nevertheless, the origin of GDDs and their link to GDGTs remain unclear. Here we examined the concentration and distribution of iso GDDs and br GDDs, together with those of iso GDGTs and br GDGTs along a 4 m peat core from Tanzania. Whereas br GDDs have only been detected to date in their core lipid (CL) form, we report here, for the first time, br GDDs in both CL and intact polar lipid (IPL) forms, suggesting a biosynthetic origin for br GDDs. Concentrations of br GDGTs and br GDDs on one hand and of iso GDGTs and iso GDDs on the other hand, were observed to significantly co-vary (R2 0.49–0.58; p < 0.05), both for the CL and IPL fractions. Moreover, the fractional abundance of each GDD correlated significantly with that of its GDGT analogue (R2 0.33–0.97; p < 0.05). Taken together, the data show that GDDs and GDGTs are closely related and likely take part in common metabolic pathways, although the hypothesis of GDDs being degradation products of GDGTs cannot be excluded.  相似文献   

8.
Over the last years a novel group of branched glycerol dialkyl glycerol tetraether (GDGT) membrane lipids has been discovered in peat bogs and soils. They consist of components with 4-6 methyl groups attached to the n-alkyl chains and 0 to 2 cyclopentyl moieties in the alkyl chain. These branched membrane lipids are produced by an as yet unknown group of anaerobic soil bacteria. In this study we analysed the branched membrane lipid content of 134 soil samples from 90 globally distributed locations to study the environmental factors controlling the relative distribution of the different branched GDGT isomers. Our results show that the relative amount of cyclopentyl moieties, expressed in the cyclisation ratio of branched tetraethers (CBT), is primarily related to the pH of the soil (R2 = 0.70) and not to temperature (R2 = 0.03). The relative amount of methyl branches, expressed in the methylation index of branched tetraethers (MBT), is positively correlated with the annual mean air temperature (MAT) (R2 = 0.62) and, to a lesser extent, negatively correlated with the pH of the soil (R2 = 0.37). If both parameters are combined, however, it appears that the variation in the MBT is largely explained by both MAT and pH (R2 = 0.82). These results suggest that the relative distribution of soil-derived GDGT membrane lipids can be used in palaeoenvironmental studies to estimate past annual MAT and soil pH.  相似文献   

9.
Branched glycerol dialkyl glycerol tetraether (GDGT) membrane lipids occur in soils and peat bogs and are assumed to be produced by anaerobic bacteria. Two indices based on the distribution of these lipids in soils, the Cyclisation of Branched Tetraethers (CBT) and the Methylation of Branched Tetraethers (MBT) index have been shown to linearly relate to pH, and to mean annual air temperature (MAT) and pH, respectively. To directly evaluate the impact of changes in soil temperature on the MBT/CBT proxy, we determined these indices in soils sampled from a transect away from two hot springs in California, which provided a set of soils similar in composition but with different temperatures (12–41 °C). The CBT values of these geothermally heated soils show a good relation with pH (R2 0.76), similar to that of a global MBT/CBT calibration set. Also, the relationship between MBT, soil pH and temperature for the geothermally heated soils is similar to that of a global soil calibration set, although the intercept for the geothermally heated soils is significantly lower, likely because our data set is based on in situ soil temperatures rather than MAT. The results confirm the dependence of the MBT index on soil temperature and pH and support the applicability of the MBT/CBT indices as a proxy for continental palaeotemperatures and past soil pH.  相似文献   

10.
Significant amounts of sulfuric acid (H2SO4) rich saline water can be produced by the oxidation of sulfide minerals contained in inland acid sulfate soils (IASS). In the absence of carbonate minerals, the dissolution of phyllosilicate minerals is one of very few processes that can provide long-term acid neutralisation. It is therefore important to understand the acid dissolution behavior of naturally occurring clay minerals from IASS under saline–acidic solutions. The objective of this study was to investigate the dissolution of a natural clay-rich sample under saline–acidic conditions (pH 1–4; ionic strengths = 0.01 and 0.25 M; 25 °C) and over a range of temperatures (25–45 °C; pH 1 and pH 4). The clay-rich sample referred to as Bottle Bend clay (BB clay) used was from an IASS (Bottle Bend lagoon) in south-western New South Wales (Australia) and contained smectite (40%), illite (27%), kaolinite (26%) and quartz (6%). Acid dissolution of the BB clay was initially rapid, as indicated by the fast release of cations (Si, Al, K, Fe, Mg). Relatively higher Al (pH 4) and K (pH 2–4) release was obtained from BB clay dissolution in higher ionic strength solutions compared to the lower ionic strength solutions. The steady state dissolution rate (as determined from Si, Al and Fe release rates; RSi, RAl, RFe) increased with decreasing solution pH and increasing temperature. For example, the highest log RSi value was obtained at pH 1 and 45 °C (−9.07 mol g−1 s−1), while the lowest log RSi value was obtained at pH 4 and 25 °C (−11.20 mol g−1 s−1). A comparison of these results with pure mineral dissolution rates from the literature suggests that the BB clay dissolved at a much faster rate compared to the pure mineral samples. Apparent activation energies calculated for the clay sample varied over the range 76.6 kJ mol−1 (pH 1) to 37.7 kJ mol−1 (pH 4) which compare very well with the activation energy values for acidic dissolution of monomineralic samples e.g. montmorillonite from previous studies. The acid neutralisation capacity (ANC) of the clay sample was calculated from the release of all structural cations except Si (i.e. Al, Fe, K, Mg). According to these calculations an ANC of 1.11 kg H2SO4/tonne clay/day was provided by clay dissolution at pH 1 (I = 0.25 M, 25 °C) compared to an ANC of 0.21 kg H2SO4/tonne clay/day at pH 4 (I = 0.25 M, 25 °C). The highest ANC of 6.91 kg H2SO4/tonne clay/day was provided by clay dissolution at pH 1 and at 45 °C (I = 0.25 M), which is more than three times higher than the ANC provided under the similar solution conditions at 25 °C. In wetlands with little solid phase buffering available apart from clay minerals, it is imperative to consider the potential ANC provided by the dissolution of abundantly occurring phyllosilicate minerals in devising rehabilitation schemes.  相似文献   

11.
This study of five small (<3.0 ha) lakes in southwestern Greenland examines the veracity of branched glycerol dialkyl glycerol tetraethers (br GDGTs) as a temperature proxy in lacustrine systems. The proximity (<5 km) of the lakes suggests that their temperature history, and thus their br GDGT records, should be similar. Distributions of br GDGTs in (i) surface sediments from all five lakes, (ii) 14C-dated sediment cores from two lakes (Upper and Lower EVV Lakes) and (iii) soil samples from the area surrounding the lakes were examined. The temporal records of br GDGT-based temperature for the two cores exhibited both similarities and major discrepancies. The differences between the paleotemperature records for the two lakes suggest that br GDGTs are not solely soil-derived, reflecting air temperature, but also indicate an additional br GDGT contribution from another source. Among the broader suite of lake sediments, there was a strong correlation (R2 0.987) between br GDGT-based surface sediment temperatures and measured summer bottom water temperatures for the four lakes with hypoxic/anoxic bottom waters, including Upper EVV Lake. The correlation suggests production of br GDGTs by anaerobic bacteria within the bottom water and/or sediment–water interface, reflecting environmental temperature for the individual lakes and augmenting the uniform, soil-derived signal. Hence, assessment of br GDGTs in Greenland lake sediments provides evidence for their origin from anaerobic autochthonous bacteria and indicates that interpretation of lacustrine br GDGT-based paleotemperature records requires contextual knowledge of individual lake systems and potential source(s) of sedimentary br GDGTs.  相似文献   

12.
Lumbricus terrestris earthworms exposed to 11 soils of contrasting properties produced, on average, 0.8 ± 0.1 mgCaCO3 earthworm?1 day?1 in the form of granules up to 2 mm in diameter. Production rate increased with soil pH (r2 = 0.68, p < 0.01). Earthworms could be a significant source of calcite in soils.  相似文献   

13.
Radiocarbon dates from known age, pre-bomb eastern oyster (Crassostrea virginica) shells provide local marine reservoir corrections (?R) for Chesapeake Bay and the Middle Atlantic coastal area of eastern North America. These data suggest subregional variability in ?R, ranging from 148 ± 46 14C yr on the Potomac River to ? 109 ± 38 14C yr at Swan Point, Maryland. The ?R weighted mean for the Chesapeake's Western Shore (129 ± 22 14C yr) is substantially higher than the Eastern Shore (? 88 ± 23 14C yr), with outer Atlantic Coast samples falling between these values (106 ± 46 and 2 ± 46 14C yr). These differences may result from a combination of factors, including 14C-depleted freshwater that enters the bay from some if its drainages, 14C-depleted seawater that enters the bay at its mouth, and/or biological carbon recycling. We advocate using different subregional ?R corrections when calibrating 14C dates on aquatic specimens from the Chesapeake Bay and coastal Middle Atlantic region of North America.  相似文献   

14.
High-frequency spectral decay factor, kappa (k), in the accelerograms of the Wenchuan mainshock was measured using strong motion data from 52 stations within 311 km of the epicenter. The derived k range from 0.0034 s to 0.0468 s. The correlation of k versus fault distance was given, which is k = 0.01288 + 5.9068 × 10–5 R for the N-S component, k = 0.01881 + 1.4219 × 10–5 R for the E-W component, and k = 0.00855 + 5.6086 × 10–5 R for the U-D component. The analysis on the spatial variation of k demonstrates that k relates to source effect and propagation effect besides local site effect. Ground motions for the 52 stations were simulated using derived k and compared to actual recordings in terms of waveforms, amplitude spectra and response spectra. The results show agreement at shorter periods (<1 s), but a slight overestimation at longer periods (1–7 s).  相似文献   

15.
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   

16.
Small angle neutron scattering techniques have been applied to investigate the phase behavior of CO2 injected into coal and possible changes in the coal pore structure that may result from this injection. Three coals were selected for this study: the Seelyville coal from the Illinois Basin (Ro = 0.53%), Baralaba coal from the Bowen Basin (Ro = 0.67%), and Bulli 4 coal from the Sydney Basin (Ro = 1.42%). The coals were selected from different depths to represent the range of the underground CO2 conditions (from subcritical to supercritical) which may be realized in the deep subsurface environment. The experiments were conducted in a high pressure cell and CO2 was injected under a range of pressure conditions, including those corresponding to in-situ hydrostatic subsurface conditions for each coal. Our experiments indicate that the porous matrix of all coals remains essentially unchanged after exposure to CO2 at pressures up to 200 bar (1 bar = 105 Pa). Each coal responds differently to the CO2 exposure and this response appears to be different in pores of various sizes within the same coal. For the Seelyville coal at reservoir conditions (16 °C, 50 bar), CO2 condenses from a gas into liquid, which leads to increased average fluid density in the pores (ρpore) with sizes (r) 1 × 105 ≥ r ≥ 1 × 104 Å (ρpore ≈ 0.489 g/cm3) as well as in small pores with size between 30 and 300 Å (ρpore ≈ 0.671 g/cm3). These values are by a factor of three to four higher than the density of bulk CO2 (ρCO2) under similar thermodynamic conditions (ρCO2 ≈ 0.15 g/cm3). At the same time, in the intermediate size pores with r ≈ 1000 Å the average fluid density is similar to the density of bulk fluid, which indicates that adsorption does not occur in these pores. At in situ conditions for the Baralaba coal (35 OC, 100 bar), the average fluid density of CO2 in all pores is lower than that of the bulk fluid (ρpore / ρCO2 ≈ 0.6). Neutron scattering from the Bulli 4 coal did not show any significant variation with pressure, a phenomenon which we assign to the extremely small amount of porosity of this coal in the pore size range between 35 and 100,000 Å.  相似文献   

17.
The Southern Alps are an ideal locality for studying patterns of isotopic fractionation associated with orographic precipitation. We have evaluated whether altitudinal change is reflected in the stable hydrogen isotopic composition (δ2H) of stream water, plant stem water and leaf wax lipids (n-alkanes) from living plants and soils, as well as in soil temperature. Samples were collected along an altitudinal transect from the windward side of the Southern Alps to Lake Hawea in the rain shadow. The results indicate that δ2H values of stem water overlap with stream water, demonstrating a gradual decrease with elevation that complied with modeled Rayleigh distillation, reflecting an isotopic lapse rate of −18.0 (± 1.1, 1σ)‰/km. Leaf and soil n-alkanes shared similar δ2H values and were 2H depleted relative to stem/stream waters. The values for soil n-alkanes indicated an isotopic lapse rate of −21.8 (± 2.0, 1σ)‰/km, consistent with precipitation data and long term observations. MBT/CBT derived soil temperature values based on the relative distribution of microbial tetraether lipids were similar to midsummer temperature observations, displaying an elevational decrease rate of −5.6 (± 1.5, 1σ) °C/km, consistent with regional and global observations.The results indicate that sedimentary lipid δ2H and microbial tetraether temperature estimates captured altitudinal trends in the isotopic composition of precipitation and mean temperature and further support their application in the reconstruction of past climate and surface uplift histories. However, notable differences in isotopic composition and temperature estimates between in situ soils and those with downslope transport of material emphasize the importance of facies analysis when interpreting past systems.  相似文献   

18.
Four dense Scandinavian limestones were analyzed to determine their mechanical properties. The generation of dust (? 10 μm) and fines (? 90 μm) during a closed circuit vertical roller mill comminution process was correlated with the calcite crystal size distributions of each limestone. Thin sections were analyzed and by means of stereology the calcite crystal size distributions for each limestone was measured. The dust generation of limestones is governed by a surface abrasive mechanism (R2 = 0.99) and the production of fines is governed by the mechanical strength of limestones (R2 = 0.99). The overall limestone degradation mechanism is predominantly controlled by the calcite cleavage planes which reduce the power consumption during the comminution process. This study is the first step in determining the influence of limestone texture on the wear rates in heterogenous raw mixes used in closed circuit comminution equipment.  相似文献   

19.
《Applied Geochemistry》2006,21(10):1760-1780
Sulfide-rich mine tailings in Adak that are exposed to weathering cause acid mine drainage characterized by low pH (2–4) and high SO4 (up to 800 mg L−1). Surface water, sediment and soil samples collected in this study contain higher concentrations of As, Cu, Fe and Zn, compared to the target and/or intervention limits set by international regulatory agencies. In particular, high As concentrations in water (up to 2900 μg L−1) and sediment (up to 900 mg kg−1) are of concern. There is large variability in trace element concentrations, implying that both physical (grain size) and chemical factors (pH, secondary phases as sulfides, Al-oxides or clay minerals) play an important role in their distribution. The low pH keeps the trace elements dissolved, and they are transported farther downstream. Trace element partition coefficients are low (log Kd = 0.3–4.3), and saturation indices calculated with PHREEQC are <0 for common oxide and sulfidic minerals. The sediment and soil samples indicate an enhanced pollution index (up to 17), and high enrichment factors for trace elements (As up to 38,300; Zn up to 800). Finally, leaves collected from different plant types indicate bioaccumulation of several elements (As, Al, Cu, Fe and Zn). However, some of the plants growing in this area (e.g., Salix, Equisétum) are generally resistant to metal toxicity, and hence, liming and phytoremediation could be considered as potential on-site remediation methods.  相似文献   

20.
The linkage between the iron and the carbon cycles is of paramount importance to understand and quantify the effect of increased CO2 concentrations in natural waters on the mobility of iron and associated trace elements. In this context, we have quantified the thermodynamic stability of mixed Fe(III) hydroxo-carbonate complexes and their effect on the solubility of Fe(III) oxihydroxides. We present the results of carefully performed solubility measurements of 2-line ferrihydrite in the slightly acidic to neutral–alkaline pH ranges (3.8–8.7) under constant pCO2 varying between (0.982–98.154 kPa) at 25 °C.The outcome of the work indicates the predominance of two Fe(III) hydroxo carbonate complexes FeOHCO3 and Fe(CO3)33−, with formation constants log*β°1,1,1 = 10.76 ± 0.38 and log β°1,0,3 = 24.24 ± 0.42, respectively.The solubility constant for the ferrihydrite used in this study was determined in acid conditions (pH: 1.8–3.2) in the absence of CO2 and at T = (25 ± 1) °C, as log*Ks,0 = 1.19 ± 0.41.The relative stability of the Fe(III)-carbonate complexes in alkaline pH conditions has implications for the solubility of Fe(III) in CO2-rich environments and the subsequent mobilisation of associated trace metals that will be explored in subsequent papers.  相似文献   

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