Dynamics of soil extractable carbon and nitrogen under different cover crop residues

Purpose

Cover crop residue is generally applied to improve soil quality and crop productivity. Improved understanding of dynamics of soil extractable organic carbon (EOC) and nitrogen (EON) under cover crops is useful for developing effective agronomic management and nitrogen (N) fertilization strategies.

Materials and methods

Dynamics of soil extractable inorganic and organic carbon (C) and N pools were investigated under six cover crop treatments, which included two legume crops (capello woolly pod vetch and field pea), three non-legume crops (wheat, Saia oat and Indian mustard), and a nil-crop control (CK) in southeastern Australia. Cover crops at anthesis were crimp-rolled onto the soil surface in October 2009. Soil and crop residue samples were taken over the periods October?CDecember (2009) and March?CMay (2010), respectively, to examine remaining crop residue biomass, soil NH₄ ⁺?N and NO₃ ^??CN as well as EOC and EON concentrations using extraction methods of 2?M KCl and hot water. Additionally, soil net N mineralization rates were measured for soil samples collected in May 2010.

Results and discussion

The CK treatment had the highest soil inorganic N (NH₄ ⁺?N?+?NO₃ ^??CN) at the sampling time in December 2009 but decreased greatly with sampling time. The cover crop treatments had greater soil EOC and EON concentrations than the CK treatment. However, no significant differences in soil NH₄ ⁺?N, NO₃ ^??CN, EOC, EON, and ratios of EOC to EON were found between the legume and non-legume cover crop treatments across the sampling times, which were supported by the similar results of soil net N mineralization rates among the treatments. Stepwise multiple regression analyses indicated that soil EOC in the hot water extracts was mainly affected by soil total C (R ²?=?0.654, P?<?0.001), while the crop residue biomass determined soil EON in the hot water extracts (R ²?=?0.591, P?<?0.001).

Conclusions

The cover crop treatments had lower loss of soil inorganic N compared with the CK treatment across the sampling times. The legume and non-legume cover crop treatments did not significantly differ in soil EOC and EON pools across the sampling times. In addition, the decomposition of cover crop residues had more influence on soil EON than the decomposition of soil organic matter (SOM), which indicated less N fertilization under cover crop residues. On the other hand, the decomposition of SOM exerted more influence on soil EOC across the sampling times among the treatments, implying different C and N cycling under cover crops.     

Optimization of arsenic and pentachlorophenol removal from soil using an experimental design methodology

Purpose

In this study, a soil-washing process was investigated for arsenic (As) and pentachlorophenol (PCP) removal from polluted soils. This research first evaluates the use of chemical reagents (HCl, HNO₃, H₂SO₄, lactic acid, NaOH, KOH, Ca(OH)₂, and ethanol) for the leaching of As and PCP from polluted soils.

Materials and methods

A Box–Behnken experimental design was used to optimize the main operating parameters for soil washing. A laboratory-scale leaching process was applied to treat four soils polluted with both organic ([PCP] _i ?=?2.5–30 mg kg^?1) and inorganic ([As] _i ?=?50–250 mg kg^?1, [Cr] _i ?=?35–220 mg kg^?1, and [Cu] _i ?=?80–350 mg kg^?1) compounds.

Results and discussion

Removals of 72–89, 43–62, 52–68, and 64–98 % were obtained for As, Cr, Cu, and PCP, respectively, using the optimized operating conditions ([NaOH]?=?1 N, [cocamidopropylbetaine] _i ?=?2 % w w^?1, t?=?2 h, T?=?80 °C, and PD?=?10 %).

Conclusions

The use of NaOH, in combination with the surfactant, is efficient in reducing both organic and inorganic pollutants from soils with different levels of contamination.     

Simultaneous measurement of soil organic and inorganic carbon: evaluation of a thermal gradient analysis

Purpose

The best method for determining soil organic carbon (SOC) in carbonate-containing samples is still open to debate. The objective of this work was to evaluate a thermal gradient method (ThG), which can determine simultaneously inorganic carbon (SIC) and SOC in a wide range of soil samples.

Materials and methods

The determination of SOC by ThG (SOC_ThG) was compared to the following widespread standard methods: (1) acidification (ACI) as pretreatment and subsequent dry combustion (SOC_ACI) and (2) volumetric quantification of SIC by a calcimeter (CALC) and subtraction of the total carbon content as determined by dry combustion (SOC_CALC). Precision (F test) and bias (t test) were tested on a subset of seven samples (n?=?3). Comparison of the ThG and CALC methods was performed by regression analysis (n?=?76) on samples representing a wide range of SOC (5.5 to 212.0 g kg^?1) and SIC (0 to 59.2 g kg^?1) contents.

Results and discussion

Tests on the replicated subset showed that the precision of ThG was not significantly different from ACI or CALC (F values?<?39, n?=?3) for SOC and SIC measurements. However, SOC_ACI and SOC_CALC contents were systematically and significantly lower compared to SOC_ThG contents. The positive bias for SOC_ThG relative to SOC_CALC contents appeared also in the regression analysis (given numbers?±?standard errors) of the whole data set (y?=?(4.67?±?0.70)?+?(0.99?±?0.01)x, R ²?=?0.99, n?=?76). When performing a regression with carbonate-free samples, the bias between the methods was negative (?2.90?±?0.63, n?=?29) but was positive in the set with carbonate-containing samples (3.95?±?1.41, n?=?47). This observation corroborated the suspicion that the use of acid for carbonate decomposition can lead to an underestimation of SOC.

Conclusions

All methods were suitable for differentiation between SIC and SOC, but the use of acid resulted in lower estimates of SOC contents. When comparing soil samples with different carbonate concentrations, the use of the ThG method is more reliable.     

Distribution of total mercury in coastal sediments from Jade Bay and its catchment, Lower Saxony, Germany

Purpose

Sediment cores provide a reliable record of mercury (Hg) contamination and can be used to study long-term Hg pollution and relevant environmental change. In the last hundred years, there were several events which may have contributed to the accumulation of Hg in Jade Bay and its catchment. This work was undertaken to assess the record in total Hg (THg) content in sediments of cores from Jade Bay and its catchment.

Materials and methods

A 5-m sediment core from Jade Bay, Lower Saxonian Wadden Sea, southern North Sea and a 12-m core from its catchment area (Wangerland, coastal zone of the Jade Bay) were used to study Hg contents in sediments. Total Hg, grain size distribution, aluminium (Al) and total organic carbon (TOC) were analysed on subsamples of both sediment cores. Total Hg was determined by oxygen combustion-gold amalgamation using DMA-80.

Results and discussion

As THg contents of the Jade Bay core were positively correlated to the sum of TOC and Al contents (r ²?=?0.86, p?<?0.001), the Hg data were interpreted using a regional normalisation function with the sum of Al and TOC as the normalisation parameters. Total Hg contents of the Wangerland core were correlated better to Al contents (r ²?=?0.70, p?<?0.001) than to the sum of TOC and Al contents (r ²?=?0.63, p?<?0.05). Therefore, Hg contents in sediments of the Wangerland core were normalised to Al contents. Comparison between enrichment factors and the background range of the sediment cores suggested that Jade Bay was contaminated about 50 years ago, and that Wangerland, or the catchment area of Jade Bay, was contaminated about 300 years ago, if no diagenetic remobilization occurred.

Conclusions

Total Hg contents of both cores were low and of no concern to the aquatic environment of Jade Bay. The Hg record was in good agreement with the history of industrial development in the region; thus, Hg deposition could have occurred through atmospheric input, ammunition residues of the Second World War and volcanic emanations, as well as through diagenetic remobilization.     

Soil organic carbon stocks in Veracruz State (Mexico) estimated using the 1:250,000 soil database of INEGI: biophysical contributions

Purpose

In this study, we quantified soil organic carbon (SOC) stocks and analyzed their relationship with biophysical factors and soil properties.

Materials and methods

The study region was Veracruz State, located in the eastern part of Mexico, covering an area of 72,410 km². A soil database that contains physicochemical analyses of soil horizons such as carbon concentration data was the source of information used in this study. The database consisted of 163 soil profiles representing 464 genetic horizons. Statistical analysis was used to investigate the effect of each factor (climate, altitude, slope) on SOC stock to 0.50 m depth and to assess differences in the distribution of SOC stock in terms of soil depth (0.0–0.20, 0.20–0.40, 0.40–0.60, 0.60–0.80, 0.80–1.0 m) and land use. In order to compute the spatial distribution of SOC stock to 0.50 m depth based on the soil sampling location, the kriging method was used.

Results and discussion

Results indicated that SOC stock (0.50 m depth) ranged between 0.44 and 41.2 kg C m^?2. Regression analysis showed that SOC stocks (0.50 m depth) are negatively correlated with temperature (r?=??0.38; P?<?0.001) and positively correlated with altitude (r?=?0.40; P?<?0.001) and slope (r?=?0.40; P?<?0.001). In addition, by multiple regression, temperature combined with precipitation explained more SOC stock variations (r?=?0.43; P?<?0.001) than the regression model with precipitation (r?=?0.13; P?=?0.16) alone. Also, slope combined with temperature and precipitation explained more SOC stock variations (r?=?0.46; P?<?0.001) than the regression model with slope alone. Forest lands, grasslands, and croplands have higher SOC stocks in the 0.0–0.20-m soil layer than in deeper layers. On average, forest lands, grasslands, croplands, and other lands (wetland and dunes) had a SOC stock of 13.6, 14.6, 15.1, and 8.5 kg C m^?2 at 1 m depth, respectively. Soil color correlated (?0.25 ≤ r ≤ ?0.89) with SOC content.

Conclusions

Overall, these results indicate the influence of major interactions between biophysical factors and SOC stocks. This research indicated that SOC stock decreased with soil depth, but with slight variations depending on land use. Thus, there remains a need for more SOC data that include an improved distribution of soil sampling points in order to entirely understand the contributions of biophysical factors to SOC stocks in Veracruz State.     

Streamwater Particulate Mercury and Suspended Sediment Dynamics in a Forested Headwater Catchment

Due to the inherent differences in bioavailability and transport properties of particulate and dissolved mercury (Hg_P and Hg_D), it is important to understand the processes by which each is mobilized from soil to stream. Currently, there is a paucity of Hg_P data in the literature despite the fact that it can be the dominant fraction in some systems. We analyzed Hg_P in conjunction with volatile solids (VS, an estimate of organic content) and total suspended solids (TSS) and investigated the viability of using turbidity as a surrogate measure of Hg_P. Samples were collected for flow conditions ranging from 72 to 8,223 L?s^?1 during October 2009 through March 2010 in a 10.5-km² forested headwater catchment. Total Hg concentrations ranged from 0.28 to 49.60 ng L^?1, with the relative amount of Hg_P increasing with discharge from approximately 40% to 97%. Storm dynamics of Hg_P and Hg_D were not consistent, indicating unique controls on the export of each fraction. During high-flow events, Hg_P was consistently higher on the rising limb of the hydrograph compared with the receding limb for a range of discharge events, with this hysteresis contributing to a degraded relationship between Hg_P and streamflow. Overall, Hg_P was strongly positively correlated with VS (r ²?=?0.97), confirming the known association with organic carbon. Due to a consistent organic fraction of the suspended solids (34?±?6%), Hg_P was also well correlated with TSS (r ²?=?0.95), with an average of 0.10 ng of Hg_P per milligram of TSS in this system. Stream turbidity measured with an in situ sonde also had a strong correlation with TSS (r ²?=?0.91), enabling commutative association with VS (r ²?=?0.86) and Hg_P (r ²?=?0.76). Turbidity can explain more than twice the temporal variance in Hg_P concentrations (n?=?50) compared with discharge (r ²?=?0.76 versus 0.36), which leads to improved monitoring of Hg_P dynamics and quantification of mass fluxes.     

Mercury volatilization from a floodplain soil during a simulated flooding event

Purpose

Middle-European floodplain soils are often contaminated with mercury (Hg) and periodically flooded. In this study, the influence of a flooding event and subsequent dewatering on the volatilization of elemental Hg and methylated species was investigated in a laboratory experiment.

Material and methods

Undisturbed soil cores were taken from a topsoil (12.1?±?0.75 mg kg^?1 Hg) at the Elbe River in Lower Saxony, Germany. Soil columns were incubated at 20 °C with varying soil moisture (water-saturated for 2 weeks, 95 and 90 % water content for 1 week each), and the redox potential (E_H) was recorded. The gaseous Hg that accumulated in the headspace of the flux chamber of the columns was pumped over cooled traps filled with adsorber material and analyzed by gas chromatography/inductively coupled plasma mass spectrometry for the various Hg species.

Results and discussion

The watering of the soil resulted in a rapid decrease in the E_H and the achievement of strongly reducing conditions (E_H??1 Hg at the beginning to 5.78 μg L^?1 Hg at the end of the experiment. Species analyses revealed that exclusively elemental Hg volatilized. The volatilization rate was between 1.73 and 824 ng m^?2 h^?1 Hg, which is consistent with other studies at the Elbe River.

Conclusions

Even when flooded for a longer period of time, floodplain soils should show neither emission of methylated Hg nor exceptionally high volatilization of elemental Hg.     

Sorption isotherms and kinetics of Sb(V) on several Chinese soils with different physicochemical properties

Purpose

Sorption of antimony on soils is the primary factor that influences its immobilization and migration in the environment. In the present study, the sorption of Sb(V) onto seven Chinese soils with different physicochemical properties was investigated for exploring the relationship between the sorption capacity of Sb(V) and the physicochemical properties of the soils.

Materials and methods

Sorption isotherms and kinetics experiments were performed to ascertain the sorption capacity and the kinetic rate, respectively. The relationship between the sorption capacity of Sb(V) and the physicochemical properties of the soils was analyzed by multiple linear regressions.

Results and discussion

The results showed that the sorption isotherms fitted with both the Langmuir and Freundlich equations very well (R ²?=?0.936–0.997), and the sorption kinetic of Sb(V) onto the seven Chinese soils followed a pseudo-second-order reaction. The maximum sorption capacity of Sb(V) on the soils ranged from 134 to 1,333 mg?kg^?1. Nearly 94 % of the variability in maximum sorption of Sb(V) modeled by Freundlich equation could be described by Fe_DCB (dithionite–citrate–bicarbonicum extractable), and nearly 98 % of the variability could be described by Fe_DCB and Al_DCB.

Conclusions

Multiple linear regressions can be successfully applied to analyzing the relationship between sorption capacity and soil properties. Fe_DCB and Al_DCB played important roles in Sb(V) sorption onto soils. It would be useful to understand the environmental behaviors of Sb and for the implementation of risk assessment management and remediation strategies of Sb.     

Formation and distribution of methylmercury in sediments at a mariculture site: a mesocosm study

Purpose

The aim of the present study was to investigate the differences of methylmercury (MeHg) formation and distribution between mariculture (aquaculture) sediments (MS) and reference sediments (RS) collected from a site in Hong Kong.

Materials and methods

The MS and RS samples were split into four batches, three of which were spiked with HgCl₂ aqueous solution to a concentration of 0.8, ,2 and 8 mg k g^?1 in sediment samples SP1, SP2, and SP3, respectively, while the rest served as a control batch (referred to as C).

Results and discussion

The results showed that the highly Hg-polluted sediment produced greater amounts of MeHg. During the culture period, MeHg concentrations in sediments decreased over time. The decreasing percentage increased in the order of SP3?<?SP2?<?SP1, which might be due to the inhibition of MeHg degradation by high Hg concentrations. The mean value of MeHg concentrations and %MeHg of the total Hg (THg) in MS was significantly lower than those in RS, possibly due to the complexation of Hg with organic ligands, leading to lower Hg bioavailability for methylation bacteria. The distribution coefficient of THg (K_dT) was relatively high in MS compared to RS, indicating that the former had a greater number of binding sites for Hg adsorption.

Conclusions

Methylmercury formation was inhibited in MS, probably due to increased complexation of Hg²⁺ with organic matter and adsorption of Hg to MS. Furthermore, the mean value of K_dT in MS was relatively high when compared to RS, which illustrates that MS sediments have more binding sites than RS for adsorption of Hg.     

Production and consumption of N2O during denitrification in subtropical soils of China

Purpose

Nitrous oxide (N₂O) production and reduction rates are dependent on the interactions with each other and it is therefore important to evaluate them within the context of simultaneously operating N₂O emission and reduction. The objective of this study was to quantify the simultaneously occurring N₂O emission and reduction across a range of subtropical soils in China, to gain a mechanistic understanding of potential N₂O dynamics under the denitrification condition and their important drivers, and to evaluate the potential role of the subtropical soils as either sources or sinks of N₂O through denitrification.

Materials and methods

Soils (45, from a range of different land uses and soil parent materials) were collected from the subtropical region of Jiangxi Province, China, and tested for their potential capacity for N₂O emission and N₂O reduction to N₂ during denitrification. N₂O emission and reduction were determined in a closed system under N₂ headspace after the soils were treated with 200?mg?kg^?1 NO ₃ ^? -N and incubation at 30?°C for 28?days. The soil physical and chemical properties, the temporal variations in headspace N₂O concentration, and NO ₃ ^? -N and NH ₄ ⁺ -N concentrations in the soil slurry were measured.

Results and discussion

Variations in N₂O concentration (N) over incubation time (t) were consistent with an equation in which average R ²?=?0.84?±?0.11 (p?<?0.05): $ N = A \times \left( {1 - \exp \left( { - {k_1} \times t} \right)} \right) - B \times \exp \left( {{k_2} \times t} \right) $ , where A is the total N₂O emission during the incubation, B is a constant, and k ₁ and k ₂ are the N₂O emission constant and reduction constants, respectively. The results of the simulation showed that k ₁ was greater than k ₂. The reduced amount of NO ₃ ^? -N in the first 7?days of incubation and the N₂O emission rate (the percentage of A value relative to the amount of NO ₃ ^? -N reduced during the 28-day incubation, R _n) were able to explain 82.9?% (p?<?0.01) of the variation in total N₂O emission (A) during the incubation for the soil samples studied, indicating that the total amount of N₂O emitted was determined predominately by denitrification capacity. Soil organic carbon content and soil nitrogen mineralization are the key factors that determine differences in the amounts of reduced NO ₃ ^? -N among the soil samples. The R _n value decreased with increasing k ₂ (p?<?0.01), indicating that soils with higher N₂O reduction capacity under these incubation conditions would emit less N₂O per unit of denitrified NO ₃ ^? -N than the other soils. Results are valuable in the evaluation of net N₂O emissions in the subtropical soils and the global N budget.

Conclusions

In a closed, anaerobic system, variations in N₂O concentration in the headspace over the incubation time were found to be compatible with a nonlinear equation. Soil organic carbon and the amount of NH ₄ ⁺ -N mineralized from the organic N during the first 7?days of incubation are the key factors that determine differences in the N₂O emission constant (k ₁), the N₂O reduction constant (k ₂), the total N₂O emission during the incubation (A) and the N₂O emission rate (R _n).     

The bioaccumulation of Cd in rice grains in paddy soils as affected and predicted by soil properties

Purpose

The area of cadmium (Cd)-contaminated soil in China is increasing due to the rapid development of the Chinese economy. To ensure that the rice produced in China meets current food safety and quality standards, the current soil quality standards for paddy soils urgently need to be updated.

Materials and methods

We conducted a pot experiment with 19 representative paddy soils from different parts of China to study the effects of soil properties on bioaccumulation of Cd in rice grains. The experiment included a control, a low treatment concentration (0.3 mg kg^–1 for pH?<?6.5 and 0.6 mg kg^–1 for pH?≥?6.5), and a high treatment concentration (0.6 mg kg^–1 for pH?<?6.5 and 1.2 mg kg^–1 for pH?≥?6.5) of Cd salt added to soils.

Results and discussion

The results showed that the Cd content in grains of the control and low and high Cd treatments ranged from 0.021 to 0.14, 0.07 to 0.27, and 0.12 to 0.33 mg kg^–1, respectively. Stepwise multiple regression analysis indicated that soil pH and organic carbon (OC) content could explain over 60 % of the variance in the (log-transformed) bioaccumulation coefficient (BCF) of Cd in grains across soils. Aggregated boosted trees analysis showed that soil pH and OC were the main factors controlling Cd bioavailability in paddy soils. Validation of the models against data from recent literature indicated that they were able to accurately predict the BCF in paddy soils.

Conclusions

These quantitative relationships between the BCF of Cd in grains and soil properties are helpful for developing soil-specific guidance on Cd safety threshold value for paddy soils.     

Effects of nitrogen fertilizer on the acidification of two typical acid soils in South China

Purpose

A laboratory incubation under constant temperature and humidity was conducted to estimate the impacts of nitrogen (N) fertilizers on the acidification of two acid soils (Plinthudult and Paleudalfs) in south China.

Materials and methods

The experiment had three treatments, i.e., control (CK), addition of urea (U), and addition of ammonium sulfate (AS). We measured soil pH, nitrate (NO₃ ^?), ammonium (NH₄ ⁺), exchangeable hydrogen ion (H⁺), and aluminum ion (Al³⁺) concentrations at various intervals during the 90 days of incubation. Soil buffering capacity (pHBC) was also measured at the end of the experiment.

Results and discussion

The application of N fertilizers resulted in soil acidification. The U treatment caused greater acidification of the Plinthudult soil than the AS treatment, while there were no differences between U and AS treatments on the acidification of the Paleudalfs. At the end of the trial, the pHBC of Plinthudult in AS treatment was greater than that in CK and U treatments, which may be due to the buffering system of NH₄ ⁺ and NH₄OH. However, the pHBC of Paleudalfs was unchanged between treatments. The dynamics of exchangeable H⁺ and Al³⁺ corresponded to that of soil pH. Correlation analysis showed that both soil exchangeable H⁺ and soil exchangeable Al³⁺ were significantly related to soil pH.

Conclusions

Application of urea and ammonium sulfate caused acidification in both soils and increased soil exchangeable Al³⁺ and H⁺ concentrations in the Paleudalfs. The application of urea increased exchangeable Al³⁺, and ammonium sulfate increased pHBC in the Plinthudult.     

Influence of mixtures of acenaphthylene and benzo[a]anthracene on their degradation by Pleurotus ostreatus in sandy soil

Purpose

Polycyclic aromatic hydrocarbons (PAHs) are a class of organic compounds commonly found as soil contaminants. Fungal degradation is considered as an environmentally friendly and cost-effective approach to remove PAHs from soil. Acenaphthylene (Ace) and Benzo[a]anthracene (BaA) are two PAHs that can coexist in soils; however, the influence of the presence of each other on their biodegradation has not been studied. The biodegradation of Ace and BaA, alone and in mixtures, by the white rot fungus Pleurotus ostreatus was studied in a sandy soil.

Materials and methods

Experimental microcosms containing soil spiked with different concentrations of Ace and BaA were inoculated with P. ostreatus. Initial (t ₀) and final (after 15 days of incubation) soil concentrations of Ace and BaA were determined after extraction of the PAHs.

Results and discussion

P. ostreatus was able to degrade 57.7% of the Ace in soil spiked at 30 mg kg^?1 dry soil and 65.8% of Ace in soil spiked at 60 mg kg^?1 dry soil. The degradation efficiency of BaA by P. ostreatus was 86.7 and 77.4% in soil spiked with Ace at 30 and 60 mg kg^?1 dry soil, respectively. After 15 days of incubation, there were no significant differences in Ace concentration between soil spiked with Ace and soil spiked with Ace + BaA, irrespective of the initial soil concentration of both PAHs. There were also no differences in BaA concentration between soil spiked with BaA and soil spiked with BaA + Ace.

Conclusions

The results indicate that the fungal degradation of Ace and BaA was not influenced by the presence of each other’s PAH in sandy soil. Bioremediation of soils contaminated with Ace and BaA using P. ostreatus is a promising approach to eliminate these PAHs from the environment.     

Mercury Methylation Capacity and Removal of Hg Species from Aqueous Medium by Cyanobacteria

Most technologies used for decontamination presents good results for high concentrations, but limitations for lower ones. The desirable Hg concentration in the water is extremely low because of its toxicity. The aims of this study were to evaluate inorganic mercury (Hg²⁺) and methylmercury (CH₃Hg⁺) toxicity in Nostoc paludosum, to assess the potential of this cyanobacteria strain to remove these Hg species from aqueous medium and also to investigate Hg methylation by the cyanobacteria. CH₃Hg⁺ determination was performed by gas chromatography-pyrolysis-atomic fluorescence spectrometry in cultures exposed to a concentration of 20 μg L^?1 for 30 days. Both Hg species were removed from the supernatant, ranging from 73 to 96% of Hg²⁺ and from 73 to 95% of CH₃Hg⁺. Ultrastructural Hg²⁺ effects in the cyanobacteria cells investigated by transmission electron microscopy revealed higher production of glycogen, cyanophycin, and intrathylacoidal spaces than the control group. When Hg was added to the culture in the form of CH₃Hg⁺, a decrease corresponding to approximately 60% of the initial concentration due to Hg volatilization was observed. The production of CH₃Hg⁺ by the cyanobacteria was detected in concentrations near the limit of detection (0.0025%) of the bioaccumulated THg. This is an advantage for biotechnological decontamination applications, as CH₃Hg⁺ is a very toxic specie and can be bioaccumulated and biomagnified. The results demonstrated that cyanobacteria cells are an efficient alternative to retain and/or remove Hg at low concentrations and they constitute a potential tool for a “final cleaning” of contaminated waste water.     

The effects of mercury,copper, and zinc on calcium uptake by larvae of the clam,mulinia lateralis

A sensitive and rapid bioassay system using Ca-45 uptake by larvae of Mulinia lateralis as indicator is described. The values of Ca uptake per larva^?1 versus elapsed time were linear and some of the Ca uptake rates, expressed as pg Ca larva^?1 h^?1, were 148.2 (no added heavy metal), 114.4 (20 µg kg^?1 of added Hg), 89.7 (200 gg kg^?1 of added Zn) and 20.5 (40 µg kg^?1 of added Cu). Linearities were also obtained by plotting log of Ca uptake per larva^?1 against heavy metal concentrations. A new terminology, ^xCa _inf50 ^supt , was proposed which expressed the concentration of heavy metal, x, causing 50% depression of Ca uptake over the exposure time, t. For Cu, Hg, and Zn, the values of ^x Ca _inf50 ^sup72h were 18.5, 26.5 and 176.0 µg kg^?1 respectively, which were comparable to the published values of LC₅₀. The effectiveness of Ca uptake depression on a weight basis was Cu > Hg > Zn, and the same sequence was also observed for larval mortalities.     

Measuring the bioavailability of polychlorinated biphenyls to earthworms in soil enriched with biochar or activated carbon using triolein-embedded cellulose acetate membrane

Purpose

Polychlorinated biphenyls (PCBs) are persistent soil contaminants that resist biodegradation and present serious risks to living organisms. The presence of biochar in soils can lower the availability of PCBs to biota. In this study, the effect of biochar enrichment in soils on bioaccumulation of PCBs was investigated.

Materials and methods

We applied two types of biochar including pine needle biochar (PC) and wheat straw biochar (WC), and an activated carbon (AC) to soil (2 % w/w) and employed two alternative methods to quantified rates of bioaccumulation: a living bioassay (using earthworm, Eisenia fetida, as a model organism) and a triolein-embedded cellulose acetate membrane (TECAM).

Results and discussion

Our results show that the application of biochar or AC greatly reduced the uptake of PCBs (particularly less-chlorinated PCBs) by earthworms (the reduction in total PCBs concentration was up to 40.0 and 49.0 % for PC and WC treatments, while 71.6 % for AC application). We found that the bioaccumulation factors (BAFs) for PCBs in the earthworms in biochar/AC-enriched soils were strongly correlated with O:C ratio of the biochar/AC (R ²?=?0.998, p?<?0.05). We observed that BAFs increased at log K _OW below 6.3 and decreased at log K _OW values greater than 6.3. We demonstrated that the concentration of PCBs in TECAM membranes were positively correlated with the concentration of PCBs earthworms in soil.

Conclusions

TECAM offers an efficient and cost-effective method for predicting the bioavailability of PCBs in field-contaminated soils undergoing sorbent-based remediation.

     

Mechanisms behind the stimulation of nitrification by N input in subtropical acid forest soil

Purpose

Input of N as NH₄ ⁺ is known to stimulate nitrification and to enhance the risk of N losses through NO₃ ^? leaching in humid subtropical soils. However, the mechanisms responsible for this stimulation effect have not been fully addressed.

Materials and methods

In this study, an acid subtropical forest soil amended with urea at rates of 0, 20, 50, 100 mg N kg^?1 was pre-incubated at 25 °C and 60 % water-holding capacity (WHC) for 60 days. Gross N transformation rates were then measured using a ¹⁵N tracing methodology.

Results and discussion

Gross rates of mineralization and nitrification of NH₄ ⁺-N increased (P?<?0.05), while gross rate of NO₃ ^? immobilization significantly decreased with increasing N input rates (P?<?0.001). A significant relationship was established between the gross nitrification rate of NH₄ ⁺ and the gross mineralization rate (R ²?=?0.991, P?<?0.01), so was between net nitrification rate of NH₄ ⁺ and the net mineralization rate (R ²?=?0.973, P?<?0.05).

Conclusions

Stimulation effect of N input on the gross rate of nitrification of NH₄ ⁺-N in the acid soil, partially, resulted from stimulation effect of N input on organic N mineralization, which provides pH-favorable microsites for the nitrification of NH₄ ⁺ in acid soils (De Boer et al., Soil Biol Biochem 20:845–850, 1988; Prosser, Advan Microb Physiol 30:125–181, 1989). The stimulated gross nitrification rate with the decreased gross NO₃ ^? immobilization rate under the elevated N inputs could lead to accumulation of NO₃ ^? and to enhance the risk of NO₃ ^? loss from humid forest soils.

     

Soil carbon dioxide emission from intensively cultivated black soil in Northeast China: nitrogen fertilization effect

Purpose

The aim of this study was to understand the effect of nitrogen fertilization on soil respiration and native soil organic carbon (SOC) decomposition and to identify the key factor affecting soil respiration in a cultivated black soil.

Materials and methods

A field experiment was conducted at the Harbin State Key Agroecological Experimental Station, China. The study consisted of four treatments: unplanted and N-unfertilized soil (U0), unplanted soil treated with 225?kg?N?ha^?1 (UN), maize planted and N-unfertilized soil (P0), and planted soil fertilized with 225?kg?N?ha^?1 (PN). Soil CO₂ and N₂O fluxes were measured using the static closed chamber method.

Results and discussion

Cumulative CO₂ emissions during the maize growing season with the U0, UN, P0, and PN treatments were 1.29, 1.04, 2.30 and 2.27?Mg?C?ha^?1, respectively, indicating that N fertilization significantly reduced the decomposition of native SOC. However, no marked effect on soil respiration in planted soil was observed because the increase of rhizosphere respiration caused by N addition was counteracted by the reduction of native SOC decomposition. Soil CO₂ fluxes were significantly affected by soil temperature but not by soil moisture. The temperature sensitivity (Q ₁₀) of soil respiration was 2.16?C2.47 for unplanted soil but increased to 3.16?C3.44 in planted soil. N addition reduced the Q ₁₀ of native SOC decomposition possibly due to low labile organic C but increased the Q ₁₀ of soil respiration due to the stimulation of maize growth. The estimated annual CO₂ emission in N-fertilized soil was 1.28?Mg?C?ha^?1 and was replenished by the residual stubble, roots, and exudates. In contrast, the lost C (1.53?Mg?C?ha^?1) in N-unfertilized soil was not completely supplemented by maize residues, resulting in a reduction of SOC. Although N fertilization significantly increased N₂O emissions, the global warming potential of N₂O and CO₂ emissions in N-fertilized soil was significantly lower than in N-unfertilized soil.

Conclusions

The stimulatory or inhibitory effect of N fertilization on soil respiration and basal respiration may depend on labile organic C concentration in soil. The inhibitory effect of N fertilization on native SOC decomposition was mainly associated with low labile organic C in tested black soil. N application could reduce the global warming potential of CO₂ and N₂O emissions in black soil.     

Shift in abundance and structure of soil ammonia-oxidizing bacteria and archaea communities associated with four typical forest vegetations in subtropical region

Purpose

Nitrogen (N) is one of the most important elements that can limit plant growth in forest ecosystems. Ammonia-oxidizing bacteria (AOB) and archaea (AOA) are considered as the key drivers of global N biogeochemical cycling. Soil ammonia-oxidizing microbial communities associated with subtropical vegetation remain poorly characterized. The aim of this study was to determine how AOA and AOB abundance and community structure shift in response to four typical forest vegetations in subtropical region.

Materials and methods

Broad-leaved forest (BF), Chinese fir forest (CF), Pinus massoniana forest (PF), and moso bamboo forest (MB) were widely distributed in the subtropical area of southern China and represented typical vegetation types. Four types of forest stands of more than 30 years grew adjacent to each other on the same soil type, slope, and elevation, were chosen for this experiment. The abundance and community structure of AOA and AOB were characterized by using real-time PCR and denaturing gradient gel electrophoresis (DGGE). The impact of soil properties on communities of AOA and AOB was tested by canonical correspondence analysis (CCA).

Results and discussion

The results indicated that AOB dominated in numbers over AOA in both BF and MB soils, while the AOA/AOB ratio shifted with different forest stands. The highest archaeal and bacterial amoA gene copy numbers were detected in CF and BF soils, respectively. The AOA abundance showed a negative correlation with soil pH and organic C but a positive correlation with NO₃ ^??N concentration. The structures of AOA communities changed with vegetation types, but vegetation types alone would not suffice for shaping AOB community structure among four forest soils. CCA results revealed that NO₃ ^??N concentration and soil pH were the most important environmental gradients on the distribution of AOA community except vegetation type, while NO₃ ^??N concentration, soil pH, and organic C significantly affected the distribution of the AOB communities.

Conclusions

These results revealed the differences in the abundance and structure of AOA and AOB community associated with different tree species, and AOA was more sensitive to vegetation and soil chemical properties than AOB. N bioavailability could be directly linked to AOA and AOB community, and these results are useful for management activities, including forest tree species selection in areas managed to minimize N export to aquatic systems.     

Spatial distribution of the abundance and activity of the sulfate ester-hydrolyzing microbial community in a rape field

Purpose

Sulfur (S) plays a vital role in plant metabolism, and the detrimental impact of S deficiency in several field crops has increased over the last 30?years. The bio-availability of organic S to plant depends on arylsulfatase (ARS), a key enzyme for S mineralization in soil. In this study, we characterized the spatial variability of ARS activity in an agricultural soil cropped with the rape plant (Brassica napus). Because rape requires relatively large amounts of S per yield unit compared to most grain crops, it is very sensitive to S deprivation similarly to the other plants of the Brassicaceae family, with consequences for seed quality and yield.

Materials and methods

The spatial variability of (a) ARS activity, (b) the abundance of culturable bacteria possessing the ARS, and (c) soil properties (temperature, soil pH, SO ₄ ^2? -S (sulfate-S) content, labile carbon (C) and nitrogen (N), soil microbial biomass carbon SMB-C, and nitrogen SMB-N) was estimated at 40 sites within a rape field, using a 4?×?5-m sampling grid. Geostatistics were used to model the spatial distribution of the measured variables, and relationships between variables were tested using linear statistical analyses.

Results and discussion

The total ARS activity showed a low variability ranging between 69.0 and 153.1???g?p-nitrophenol?g^?1?dry?soil?h^?1 while the abundance of the culturable ARS community ranged within one order of magnitude. The distribution of both the abundance and activity of the ARS community exhibited spatial dependence in 800?m² agricultural field.

Conclusions

The spatial pattern of ARS activity in the field was correlated with several soil properties, and results suggest that soil pH, labile C and N, and SBM-C/SBM-N ratio were the main parameters linked to the ARS activity rather than the abundance of the culturable ARS bacterial community or the SO ₄ ^2? -S concentration.