Comparison of NTA and Elemental Sulfur as Potential Soil Amendments in Phytoremediation

The effect of NTA (nitrilotriacetic acid) and elemental sulfur (S), two soil amendments suggested for the enhancement of metal phytoavailability in phytoextraction, on heavy metal uptake by Nicotiana tabacum (tobacco) and Zea mays (maize) were studied and compared in two Zn-, Cu-, Cd -, and Pb-contaminated soils from northern Switzerland. Experiments were performed in the greenhouse with topsoil (0 to 20 cm) material from two locations, Dornach and Rafz. The Dornach soil was calcareous and had been contaminated by dust emissions from a nearby brass metal smelter. The Rafz soil, free of carbonates, had been polluted by former sewage sludge application. Soil amendments with S increased the solubility (NaNO₃ extraction) of Zn and Cd about 10-fold in Dornach soil and up to 30-fold in Rafz soil after 55 days. Zn and Cd removal by N. tabacum and Z. mays, however, increased only about 5.5- and 2.5-fold in these treatments in Rafz soil, respectively, while in the Dornach soil only a slight increase for Cd was found. Repeated NTA application increased soluble Zn, Cu, and Cd about 100-, 20-, and 19-fold in the Dornach soil and 13-, 4-, and 2-fold in the Rafz soil shortly after application. Soluble Pb was increased by NTA up to 50-fold in Rafz soil. After 90 days soluble heavy metal concentrations were only slightly elevated in both soils. Again, however, Zn, Cd, and Cu removal by N. tabacum and Z. mays increased only about 1.5- to 2.5-fold in the two soils, whereas Pb removal by N. tabacum increased about fivefold in the Rafz soil as a result of NTA application     

Transformation of urea and ammonium sulphate in different soils

Summary The transformation of urea and ammonium sulphate in Ladwa sandy loam and Balsamand sand was studied in laboratory. Urea took at least one week in sandy loam and 2 weeks in sandy soils to hydrolyse completely. The process of hydrolysis was faster in finer soil with high organic matter than in coarse soil having low organic matter. There was no nitrification upto 3 days in sandy loam and upto 7 days in sandy soils, respectively, but there was immobilization of NO₃-N during these initial periods. The NO₃-N content at the end of incubation period (35 days) was more in case of urea than in case of ammonium sulphate treated samples in sandy loam soil and reverse was true in sandy soil. The hydrolysis of urea did not follow zero or first order kinetics as proposed in previous studies.     

Leaching of Zinc,Cadmium, and Lead in a Sandy Soil Due to Application of Poultry Litter

Dissolved organic matter in poultry litter could contribute organic ligands to form complexes with heavy metals in soil. The soluble complexes with heavy metals can be transported downward and possibly deteriorate groundwater quality. To better understand metal mobilization by soluble organic ligands in poultry litter, soil columns were employed to investigate the movement of zinc (Zn), cadmium (Cd), and lead (Pb). Uncontaminated soil was amended with Zn, Cd, and Pb at rates of 400, 8, and 200 mg kg ^{? 1} soil, respectively. Glass tubes, 4.9-cm-diameter and 40-cm-long, were packed with either natural or metal-amended soil. The resulting 20-cm-long column of soils had bulk density of about 1.58 g cm ^{? 3} . Columns repacked with natural or amended soil were leached with distilled water, 0.01 M EDTA, 0.01 M CaCl ₂ , or poultry litter extract (PLE) solutions. Low amounts of Zn, Cd, and Pb were leached from natural soil with the solutions. Leaching of Zn, Cd, or Pb was negligible with distilled water. In the metal-amended soil, EDTA solubilized more Zn, Cd, and Pb than CaCl ₂ and PLE. The breakthrough curves of Zn and Pb in the PLE and CaCl ₂ were similar, indicating they have similar ability to displace Zn and Pb from soils. Compared with Zn and Cd the PLE had a small ability to solubilize Pb from metal-amended soil. Thus, the application of poultry litter on metal-contaminated soils might enhance the mobility of Zn and Cd.     

Soil Ca alters processes contributing to C and N retention in the Oa/A horizon of a northern hardwood forest

Recent studies on the effects of calcium (Ca) additions on soil carbon (C) cycling in organic soil horizons present conflicting results, with some studies showing an increase in soil C storage and others a decrease. We tested the legacy effects of soil Ca additions on C and nitrogen (N) retention in a long-term incubation of soils from a plot-scale field experiment at the Hubbard Brook Experimental Forest, NH, USA. Two levels of Ca (850 and 4250 kg Ca/ha) were surface applied to field plots as the mineral wollastonite (CaSiO₃) in summer of 2006. Two years after field Ca additions, Oa/A horizon soils were collected from field plots and incubated in the laboratory for 343 days to test Ca effects on C mineralization, dissolved organic carbon (DOC) export, and net N transformations. To distinguish mineralization of soil organic C (SOC) from that of more recent C inputs to soil, we incubated soils with and without added ¹³C-labeled sugar maple leaf litter. High Ca additions increased exchangeable Ca and pH compared to the control. While low Ca additions had little effect on mineralization of SOC or added litter C, high Ca additions reduced mineralization of SOC and enhanced mineralization of litter C. In litter-free incubations, δ¹³C of respired C was enriched in the high Ca treatment compared to the control, indicating that Ca suppressed mineralization of ¹³C-depleted SOC sources. Leaching of DOC and NH₄ ⁺ were reduced by Ca additions in litter-free and litter-amended soils. Our results suggest that Ca availability in these organic soils influences mineralization of SOC and N primarily by stabilization processes and only secondarily through pH effects on organic matter solubility, and that SOC binding processes become important only with relatively large alterations of Ca status.     

Effects of atmospheric deposition,soil pH and acidification on heavy metal contents in soils and vegetation of semi-natural ecosystems at Rothamsted Experimental Station,UK

The effects of acidification on the soil chemistry and plant availability of the metals Pb, Cd, Zn, Cu, Mn and Ni in new and archived soil and plant samples taken from the >100-year-old experiments on natural woodland regeneration (Geescroft and Broadbalk Wildernesses) and a hay meadow (Park Grass) at Rothamsted Experimental Station are examined. We measured a significant input of metals from atmospheric deposition, enhanced under woodland by 33% (Ni) to 259% (Zn); Pb deposition was greatly influenced by vehicle emissions and the introduction of Pb in petrol. The build up of metals by long-term deposition was influenced by acidification, mobilization and leaching, but leaching, generally, only occurred in soils at pH<4. Mn and Cd were most sensitive to soil acidity with effective mobilization occurring at pH 6.0–5.5 (0.01 M CaCl₂), followed by Zn, Ni and Cu at pH 5.5–5.0. Pb was not mobilized until pH<4.5. Acidification to pH 4 mobilized 60–90% of total soil Cd but this was adsorbed onto ion exchange surfaces and/or complexed with soil organic matter. This buffering effect of ion exchange surfaces and organic matter in soils down to pH 4 was generally reflected by all the metals investigated. For grassland the maximum accumulation of metals in herbage generally corresponded to a soil pH of 4.0. For woodland the concentration of Pb, Mn and Cd in oak saplings (Quercus robur) was 3-, 4- and 6-fold larger at pH 4 than at pH 7. Mature Oak trees contained 10 times more Mn, 4 times more Ni and 3 times more Cd in their leaves at pH 4 than at pH 7. At pH values <4.0 on grassland the metal content in herbage declined. Only for Mn and Zn did this reflect a decline in the plant available soil content attributed to long-term acid weathering and leaching. The chief cause was a long-term decline in plant species richness and the increased dominance of two acid-tolerant, metal-excluder species     

Influence of rhizodeposition under elevated CO2 on plant nutrition and soil organic matter

Atmospheric CO₂ concentrations can influence ecosystem carbon storage through net primary production (NPP), soil carbon storage, or both. In assessing the potential for carbon storage in terrestrial ecosystems under elevated CO₂, both NPP and processing of soil organic matter (SOM), as well as the multiple links between them, must be examined. Within this context, both the quantity and quality of carbon flux from roots to soil are important, since roots produce specialized compounds that enhance nutrient acquisition (affecting NPP), and since the flux of organic compounds from roots to soil fuels soil microbial activity (affecting processing of SOM).From the perspective of root physiology, a technique is described which uses genetically engineered bacteria to detect the distribution and amount of flux of particular compounds from single roots to non-sterile soils. Other experiments from several labs are noted which explore effects of elevated CO₂ on root acid phosphatase, phosphomonoesterase, and citrate production, all associated with phosphorus nutrition. From a soil perspective, effects of elevated CO₂ on the processing of SOM developed under a C4 grassland but planted with C3 California grassland species were examined under low (unamended) and high (amended with 20 g m^–2 NPK) nutrients; measurements of soil atmosphere 13C combined with soil respiration rates show that during vegetative growth in February, elevated CO₂ decreased respiration of carbon from C4 SOM in high nutrient soils but not in unamended soils.This emphasis on the impacts of carbon loss from roots on both NPP and SOM processing will be essential to understanding terrestrial ecosystem carbon storage under changing atmospheric CO₂ concentrations.Abbreviations SOM soil organic matter - NPP net primary productivity - NEP net ecosystem productivity - PNPP p-nitrophenyl phosphate     

Soil nitrogen dynamics along a gradient of long-term soil development in a Hawaiian wet montane rainforest

I analyzed the rates of net N mineralization and nitrification of soils from seven sites in a Hawaiian wet montane forest. The sites differ in age, ranging from 400 to 4,100,000 yr, but are comparable in other variables (all at 1200 miasl with 4000 mm or more mean annual rainfall), and the chronosequence simulated a development of soils from basaltic lava. Soils were incubated for 20 days at 17.5 °C, which is nearly equivalent to a mean field air temperature of the sites, and at an elevated temperature of 25.5 °C under three treatments: 1) field-wet without amendments, 2) air dried to a permanent wilting point, and 3) fertilized with phosphate (NaH₂PO₄) at the rate of 50 g P per g dry soil. Both mineralization and nitrification rates varied significantly among the sites at the field temperature (p<.00001). Fractions of the mineralized organic matter (indexed by the N produced per g organic C) increased sharply from the youngest to the 5000-yr site before declining abruptly to a near constant value from the 9000 to the 1,400,000-yr sites. Total organic C in the top soils (<15 cm deep) increased almost linearly with age across the sites. Consequently, net NH₄- and NO₃-N produced on an area basis (g m^-2 20 d^-1) increased sharply from 0.2 in the youngest site to 1.2 in the 5000-yr site, then both became depressed once but steadily increased again. The fraction of organic matter mineralized, and the net N turnover rates were outstandingly high in the oldest site where a large amount of organic matter was observed; the topsoil organic matter which was used in this analysis appeared to be highly labile, whereas the subsurface organic matter could be relatively recalcitrant. As suggested by earlier workers, the initial increase in N turnover seemed to correspond to the increasing quantity of N in the soils through atmospheric deposition and biological fixation. The later decline in fraction of organic matter mineralized seemed to relate to increasing soil C/N ratios, increasingly recalcitrant organic matter, and poorer soil drainage with age. The elevated temperature treatment produced significantly higher amounts of N mineralization, except for the youngest site where N was most limiting, and for two sites where soil waterlogging might be severe. P fertilization invariably resulted in slower N turnovers, suggesting that soil microbes responded to added P causing N immobilization. The youngest site did not significantly respond to added P. The magnitude of immobilization was higher in older than in younger soils, suggesting that P more strongly limits microbial populations in the older soils.     

Interpretation of soil δ13C as an indicator of vegetation change in African savannas

Question: The relationship between carbon‐13 in soil organic matter and C₃ and C₄ plant abundance is complicated because of differential productivity, litter fall and decomposition. As a result, applying a mass balance equation to δ¹³C data from soils cannot be used to infer past C₃ and C₄ plant abundance; only the proportion of carbon derived from C₃ and C₄ plants can be estimated. In this paper, we compare δ¹³C of surface soil samples with vegetation data, in order to establish whether the ratio of C₃:C₄ plants (rather than the proportion of carbon from C₃ and C₄ plants) can be inferred from soil δ¹³C. Location: The Tsavo National Park, in southeastern Kenya. Methods: We compare vegetation data with δ¹³C of organic matter in surface soil samples and derive regression equations relating the δ¹³C of soil organic matter to C₃:C₄ plant abundance. We use these equations to interpret δ¹³C data from soil profiles in terms of changes in inferred C₃:C₄ plant ratio. We compare our method of interpretation with that derived from a mass balance approach. Results: There was a statistically significant, linear relationship between the δ¹³C of organic matter in surface soil samples and the natural logarithm of the ratio of C₃:C₄ plants in the 100m² surrounding the soil sample. Conclusions: We suggest that interpretation of δ¹³C data from organic matter in soil profiles can be improved by comparing vegetation surveys with δ¹³C of organic matter in surface soil samples. Our results suggest that past C₃ plant abundance might be under‐estimated if a mass balance approach is used.     

Cadmium and zinc adsorption maxima of geochemically anomalous soils (Oxisols) in Jamaica

Abstract

Soil samples were collected from a Miocene limestone area of Jamaica (Manchester Parish) where unusual accumulations of Cd and other metals have been described previously. The source of the metals is natural (geological). The soils are aluminous Oxisols and, geochemically, are closely similar to local karst bauxite deposits. For comparison a karst bauxite sample was collected from Alabama (USA) and an Ultisol sample from South Carolina (USA). All the Jamaican soils were in the pH range neutral to slightly alkaline and CaCO₃ contents ranged from 1.3 to 23.1%. Mean total Cd = 102.5 mg/kg (range 13.6-191.8 mg/kg) and mean Zn = 362.6 (range = 125.8-683.3) mg/kg. These values are higher than world averages. The mean readily exchangeable Cd was 0.05 (range 0.01-0.15) mmol/kg and for Zn mean = 0.02 (range 0.01-0.02) mmol/kg. Adsorption data were obtained experimentally and modelled using the Langmuir isotherm. For the Manchester soils the mean Cd adsorption maximum was 9.15 (range 2.26-32.0) mmol/kg; the values were higher than the karst bauxite sample (0.08 mmol/kg) or the Ultisol (0.08 mmol/kg). Reliable Zn isotherms were not obtained for all soils; for three Manchester soils the mean Zn sorption maximum was 2.99 mmol/kg compared with 3.13 mmol/kg for Cd in the same three soils. Mean Al and Fe values are 38.7% Al₂O₃ and 17.7% Fe₂O₃ compared with the Ultisol (14.5% Al₂O₃ 11.3% Fe₂O₃) and the bauxite (52.6% Al₂O₃, 0.7%Fe₂O₃). Interpretation of the major element values and the known mineralogy of the soils implies that the high adsorption maxima of the Manchester soils can best be explained by their calcareous nature. It is concluded that the Manchester soils have ample adsorption capacity to trap any incoming Cd or Zn solutes.     

Short-term mineralization of maize residues in soils as determined by carbon-13 natural abundance

Studies of soil organic matter equilibria must include estimates of C turnover. The objective of this study was to provide data on how the natural ¹³C abundance method can be used to determine the flow of C from C₄ residues and soil organic matter (C₃-source) in a short-term incubation. Corn residue was added at a rate of 5.7 mg C g⁻¹ soil to two soils, a clay and a sandy clay loam. During the course of a 35-day incubation in a CO₂-free system, CO₂-C and ¹³C natural abundance of the respired CO₂ were measured. About 20% of the corn residue-C added was mineralized in both soils as determined from the CO₂ respired and the ¹³C natural abundance of the respired CO₂. Mineralization of the added residues was also calculated as the difference of the total amount of the respired CO₂-C between the control and the corn residue-treated soils divided by the total amount of corn residue-C. Values were 35% for the clay soil, and 30% for the sandy clay loam soil. The difference in values calculated from the ¹³ C natural abundance and the difference method was due to mineralization of the indigenous soil organic C resulting from the addition of corn residues. Use of the natural ¹³C abundance method could determine the degree of ‘priming effect’ in soils amended with C₄-C residues. This revised version was published online in June 2006 with corrections to the Cover Date.     

Association of Microbial Community Composition and Activity with Lead, Chromium, and Hydrocarbon Contamination

Microbial community composition and activity were characterized in soil contaminated with lead (Pb), chromium (Cr), and hydrocarbons. Contaminant levels were very heterogeneous and ranged from 50 to 16,700 mg of total petroleum hydrocarbons (TPH) kg of soil⁻¹, 3 to 3,300 mg of total Cr kg of soil⁻¹, and 1 to 17,100 mg of Pb kg of soil⁻¹. Microbial community compositions were estimated from the patterns of phospholipid fatty acids (PLFA); these were considerably different among the 14 soil samples. Statistical analyses suggested that the variation in PLFA was more correlated with soil hydrocarbons than with the levels of Cr and Pb. The metal sensitivity of the microbial community was determined by extracting bacteria from soil and measuring [³H]leucine incorporation as a function of metal concentration. Six soil samples collected in the spring of 1999 had IC₅₀ values (the heavy metal concentrations giving 50% reduction of microbial activity) of approximately 2.5 mM for CrO₄²⁻ and 0.01 mM for Pb²⁺. Much higher levels of Pb were required to inhibit [¹⁴C]glucose mineralization directly in soils. In microcosm experiments with these samples, microbial biomass and the ratio of microbial biomass to soil organic C were not correlated with the concentrations of hydrocarbons and heavy metals. However, microbial C respiration in samples with a higher level of hydrocarbons differed from the other soils no matter whether complex organic C (alfalfa) was added or not. The ratios of microbial C respiration to microbial biomass differed significantly among the soil samples (P < 0.05) and were relatively high in soils contaminated with hydrocarbons or heavy metals. Our results suggest that the soil microbial community was predominantly affected by hydrocarbons.     

Effects of litter incorporation and nitrogen fertilization on the contents of extractable aluminium in the rhizosphere soil of tea plant (Camallia sinensis (L.) O. Kuntze)

The effects of litter incorporation and nitrogen application on the properties of rhizosphere and bulk soils of tea plants (Camellia sinensis (L.) O. Kuntze) were examined in a pot experiment. Total of 8 treatments included four levels of tea litter additions at 0, 4.9, 9.8, and 24.5 g kg^–1 in combination with two N levels (154.6 mg kg^–1 and without). After 18 months of growth the rhizosphere soil was collected by removing the soil adhering to plant roots and other soil was referred to as bulk soil. The dry matter productions of tea plants were significantly increased by N fertilization and litter incorporation. The effect of litter was time-depending and significantly decreased the content of exchangeable Al (Al_ex, by 1 mol L^–1 KCl) and Al saturation at 9 months after litter incorporation whereas soil pH was not affected, although the litter contained high Al content. After 18 months, the contents of extractable Al by dilute CaCl₂, CuCl₂ + KCl, NH₄OAC, ammonium oxalate and sodium citrate (Al_CaCl2, Al_Cu/KCl, Al_NH4OAC, Al_Oxal, and Al_Cit respectively) and Al_ex, were not affected by litter application, except that of Al_CaCl2 in the rhizosphere soil which was decreased following litter additions. Nitrogen fertilization with NH₄ ⁺ (urea and (NH₄)₂SO₄) significantly reduced soil pH, the contents of exchangeable Ca, K, Mg and base saturation while raised extractable Al levels (Al_CaCl2, Al_Cu/KCl, Al_NH4OAC, and Al_ex). In the rhizosphere soils exchangeable K accumulated in all treatments while exchangeable Ca and Mg depleted in treatments without litter application. The depletions of Ca and Mg were no longer observed following litter incorporation. This change of distribution gradients in rhizosphere was possibly due to the increase of nutrient supplies from litter decomposition and/or preferable root growth in soil microsites rich in organic matter. Lower pH and higher extractable Al (Al_CaCl2, Al_ex, and Al_NH4OAC) in the rhizosphere soils, regardless of N and litter treatments, were distinct and consistent in all treatments. Such enrichments of extractable Al in the rhizosphere soil might be of importance for tea plants capable of taking up large amounts of Al.     

Mobilization of cadmium from Festuca ovina roots and its simultaneous immobilization by soil in a root-soil-extractant system (in vitro test)

Mobilization of cadmium accumulated in Festuca ovina L. roots and simultaneous immobilization of this metal by soil were studied in three chambers connected into one system containing: (1) roots in an extractant solution, (2) soil in an extractant solution, and (3) extractant solution alone. Six extractants sterilized by filtration were used: 0.1 M NaNO₃ (NA), 0.1 mM desferrioxamine B (NA + DFOB) and 1 mM citric acid (NA + CA) in NA, and a water extract of soil (SE) supplemented with the same compounds. SE mobilized 53% of the Cd introduced to the system with roots. The addition of DFOB or CA to SE increased Cd extraction from roots by 17%, while the same compounds introduced to NA did not change mobilization of Cd (60% efficiency). Regardless of the extractant used, mobilization of Cd from roots was about 25% lower when extraction was done in a control system without soil. The metal released from roots was gradually immobilized by the soils loaded into all systems during a 4-day incubation. Sequential extractions of Cd from the soils showed that the metal released from roots with NA was stabilized mainly by soil Mn and Fe oxides, while that released with SE was stabilized by soil organic matter.     

Soil organic sulfur dynamics in a coniferous forest

Sulfate microbial immobilization and the mineralization of organic S were measured in vitro in soil horizons (LFH, Ae, Bhf, Bf and C) of the Lake Laflamme watershed (47°17 N, 71°14 O) using ³⁵SO₄. LFH samples immobilized from 23 to 77% of the added ³⁵SO₄ within 2 to 11 days. The ³⁵SO₄ microbial immobilization increased with temperature and reached an asymptote after a few days. The mineral soil generally immobilized less than 20% of the added ³⁵SO₄, and an asymptote was reached after 2 days. An isotopic equilibrium was rapidly reached in mineral horizons. A two-compartment (SO₄ and organic S) model adequately described ³⁵SO₄ microbial immobilization kinetics. The active organic reservoir in the whole soil profile represented less than 1% of the total organic S. The average concentrations of dissolved organic S (DOS) in the soil solutions leaving the LFH, Bhf and Bf horizons were respectively 334, 282 and 143 µgL^–1. Assuming that the DOS decrease with soil depth corresponded to the quantities adsorbed in the B horizons, we estimated that 12 800 kgha^–1 of organic S could have been formed since the last glaciation, which is about 13 times the size of the actual B horizons reservoirs. Our results suggest that the organic S reservoirs present in mineral forest soils are mostly formed by the DOS adsorption resulting from incomplete litter decomposition in the humus layer. The capability of these horizons to immobilize SO₄ from the soil solution would be restricted to a 1% active fraction composed of microorganisms. Despite their refractory nature, these reservoirs can, however, be slowly decomposed by microorganisms and contribute to the S-SO₄ export from the watershed in the long term.     

15N2 incorporation by rhizosphere soil influence of rice variety,organic matter and combined nitrogen

Summary Heterotrophic nitrogen fixation by rhizosphere soil samples from 20 rice cultivars grown under uniform field conditions was estimated employing¹⁵N-tracer technique. Rhizosphere soil samples from different rice cultivars showed striking differences with regard to their ability to incorporate¹⁵N₂. Rhizosphere samples from rice straw-amended (3 and 6 tons/ha) soil exhibited more pronounced nitrogen-fixing activity than the samples from unamended soil; while the activity of the rhizosphere samples from soils receiving combined nitrogen (40 and 80 kg N/ha) was relatively low. However, the inhibitory effect of combined nitrogen was not expressed in the presence of rice straw at 6 tons/ha. Results suggest that plant variety, application of combined nitrogen and organic matter influence the rhizosphere nitrogen fixation.     

Nitrate and dissolved organic carbon mobilization in response to soil freezing variability

Reduced snowpack and associated increases in soil freezing severity resulting from winter climate change have the potential to disrupt carbon (C) and nitrogen (N) cycling in soils. We used a natural winter climate gradient based on elevation and aspect in a northern hardwood forest to examine the effects of variability in soil freezing depth, duration, and frequency on the mobilization of dissolved organic carbon (DOC) and nitrate (NO₃ ^?) in soils over the course of 2 years. During a winter with a relatively thin snowpack, soils at lower elevation sites experienced greater freezing and especially variable freeze/thaw cycles, which in turn led to greater leaching of DOC from the organic horizon during the following growing season. In contrast to several previous field manipulation studies, we did not find changes in soil solution NO₃ ^? concentrations related to soil freezing variables. Our results are consistent with a soil matrix disturbance from freezing and thawing which increases leachable C. These results build upon previous laboratory experiments and field manipulations that found differing responses of DOC and NO₃ ^? following soil freezing, suggesting that mobilization of labile C may suppress NO₃ ^? losses through microbial immobilization of N. This research highlights the importance of studying natural variation in winter climate and soil freezing and how they impact soil C and N retention, with implications for surface water runoff quality.     

Effects of Plant Residue and Salinity on Fractions of Cadmium and Lead in Three Soils

Bioavailability and mobility of heavy metals (HMs) in soils are determined by their partitioning between solution and solid-phase and their further redistribution among solid-phase components. A study was undertaken to determine the effects of organic matter (OM) and salinity on cadmium (Cd) and lead (Pb) distribution among soil fractions. Three agricultural soils were treated with 20 mg Cd/kg as Cd (NO₃)₂·4H₂O, 150 mg Pb/kg as Pb (NO₃)₂, 20 g/kg alfalfa powder, and 50 mmol/kg of NaCl, and then incubated at 60% water holding capacity (60% WHC) and constant temperature (25°C) for 12 weeks. Various fractions of Cd and Pb were extracted from the soils after 2 and 12 w of incubation using a sequential extraction technique. Results showed that in the early stage of incubation (2 w), added Pb were found mainly in the specifically sorbed (SS) and amorphous Fe oxides (AFeO) fractions and added Cd found in SS and Mn oxides (MnO) fractions. Addition of 2% OM decreased the exchangeable (EXC) Pb fraction almost in all soils, whereas it had a different effect on the EXC Cd fraction depending on soil pH. Addition of NaCl increased the EXC Cd fraction in two soils, but it did not alter Pb fractions. At the end of the incubation period, Pb decreased in the EXC and MnO fractions except in the neutral soil and Cd decreased mainly in the SS fraction.     

Chemical changes in soil and soil solution after calcium silicate addition to a northern hardwood forest

Liming has been used to mitigate effects of acidic deposition in forest ecosystems. This study was designed to examine the effects of calcium (Ca) supply on the spatial patterns and the relations between soil and soil solution chemistry in a base-poor forest watershed. Watershed 1 at the Hubbard Brook Experimental Forest in New Hampshire, USA was experimentally treated with wollastonite (CaSiO₃) in October, 1999. Exchangeable Ca (Ex-Ca), soil pH_s (in 0.01 M CaCl₂), effective cation exchange capacity (CEC_e), and effective base saturation (BS_e) increased, while exchangeable acidity (Ex-Acid) decreased in organic soil horizons in 2000 and 2002. Mineral soils experienced either small increases in Ex-Ca, pH_s, CEC_e, BS_e, small decreases in Ex-Acid or no changes. Thus, most of the added Ca remained in the forest floor during the study period. Prior to the treatment the BS_e decreased with increasing elevation in organic and mineral soil horizons. This spatial pattern changed significantly in the forest floor after the treatment, suggesting that soils at higher elevations were more responsive to the chemical addition than at lower elevations. Soil solutions draining the forest floor responded to the treatment by increases in concentrations of Ca, dissolved silica, pH, and acid neutralizing capacity (ANC), and a decrease in inorganic monomeric Al (Al_i). Treatment effects diminished with increasing soil depth and decreasing elevation. Positive correlations between Ca/total monomeric Al (Al_m) in soil solution and Ex-Ca/Ex-Al ratios in soil indicated that changes in the chemistry of soils significantly influenced the chemistry of soil water, and that Ca derived from the dissolution of wollastonite mitigated the mobilization of Al within the experimental watershed.     

Soil Iron Content as a Predictor of Carbon and Nutrient Mobilization in Rewetted Fens

Rewetted, previously drained fens often remain sources rather than sinks for carbon and nutrients. To date, it is poorly understood which soil characteristics stimulate carbon and nutrient mobilization upon rewetting. Here, we assess the hypothesis that a large pool of iron in the soil negatively affects fen restoration success, as flooding-induced iron reduction (Fe³⁺ to Fe²⁺) causes a disproportionate breakdown of organic matter that is coupled with a release of inorganic compounds. We collected intact soil cores in two iron-poor and two iron-rich drained fens, half of which were subjected to a rewetting treatment while the other half was kept drained. Prolonged drainage led to the mobilization of nitrate (NO₃^-, > 1 mmol L^-1) in all cores, regardless of soil iron content. In the rewetted iron-rich cores, a sharp increase in pore water iron (Fe) concentrations correlated with concentrations of inorganic carbon (TIC, > 13 mmol L^-1) and dissolved organic carbon (DOC, > 16 mmol L^-1). Additionally, ammonium (NH₄⁺) accumulated up to phytotoxic concentrations of 1 mmol L^-1 in the pore water of the rewetted iron-rich cores. Disproportionate mobilization of Fe, TIC, DOC and NH₄⁺ was absent in the rewetted iron-poor cores, indicating a strong interaction between waterlogging and iron-mediated breakdown of organic matter. Concentrations of dissolved phosphorus (P) rose slightly in all cores upon rewetting, but remained low throughout the experiment. Our results suggest that large pools of iron in the top soil of drained fens can hamper the restoration of the fen’s sink-service for ammonium and carbon upon rewetting. We argue that negative effects of iron should be most apparent in fens with fluctuating water levels, as temporary oxygenation allows frequent regeneration of Fe³⁺. We conclude that rewetting of iron-poor fens may be more feasible for restoration.     

Stable isotope characteristics across narrow savanna/woodland ecotones in Wolfe Creek Meteorite Crater,Western Australia

The stable isotopic composition (δ¹³C) of sediments from lakes are frequently analyzed to reconstruct the proportion of the regional vegetation that used either the C₃ or C₄ photosynthetic pathways, often without conducting a detailed survey of the current local vegetation. We performed a study on the modern vegetation composition within the Wolfe Creek Meteorite Crater to complement our future paleoecological investigation of the crater. A bull’s-eye pattern exists where C₄ grasses dominate an outer ring and salt tolerant species, including shrubs, herbs, chenopods, and halophytic algae, dominate the inner pan of the crater. The ecotone between the inner and outer zones is narrow and occupied by tall (>7 m) Acacia ampliceps, with some C₄ grasses in the understory. Along with the highest water table and most saline soils the center of the crater has C₃ plants present with the highest δ¹³C and δ¹⁵N values. The range of δ¹³C and δ¹⁵N values from the analysis of surface soil organic matter (OM) was much smaller compared with the range of values from plant materials implying that either: (1) the current plant OM has not yet been integrated into the soils, or (2) processes within the soil have acted to homogenize isotopic variability within the crater. The application of a two end member mixing model to calculate %C₄ and %C₃ biomass from the δ¹³C of surface soil OM was complicated by: (1) the crater containing both a dry habitat with C₄ grasses and a central pan with C₄ halophytic plants and, (2) the large variation in the δ¹³C of the plants and soil OM.