Assessment of gross and net mineralization rates of soil organic phosphorus – A review

The quantification of net soil organic P mineralization rates is hampered by the potentially rapid sorption of released phosphate. Here, isotopic dilution approaches to assess gross and net organic P mineralization rates under steady-state conditions are reviewed, including different analytical and numerical solutions to assess P transformation rates based on incubation experiments with ³²P- or ³³P-labeled soils. Non-isotopic approaches are also commented on. Published isotopic dilution studies show that isotopically exchangeable P during incubation can partly or even predominantly (20–90%) result from biological and biochemical rather than physicochemical processes. The relative contribution of biological and biochemical processes tends to be lower in arable soils than under grassland and forests and is negatively related to the availability of inorganic P and positively to concentrations of soil organic carbon. Typical basal gross organic P mineralization rates range between 0.1 and 2.5 mg P kg⁻¹ d⁻¹, but rates up to 12.6 mg P kg⁻¹ d⁻¹ have been observed in grassland and forest soils. The further partitioning of gross organic P mineralization remains uncertain, but a dominance of microbial immobilization and remineralization is likely under most conditions, at least during the initial weeks of incubation. Over longer time periods, the relative importance of mineralization of non-living soil organic P increases, with the contribution of extracellular hydrolysis remaining to be elucidated. This requires other approaches than enzyme activity assays, since measurements of phosphomonoesterase activity in soil render organic P mineralization rates that are one to two orders of magnitude greater than those determined by isotopic dilution. The numerical modeling approach will enable assessment of soil P transformation rates under non-steady-state conditions, where P fluxes are likely to be greater than under steady-state conditions. Ultimately, an improved understanding of the biological and biochemical processes in soil P dynamics may help to improve P management in agroecosystems.     

Effects of vegetation on soil microbial C,N, and P dynamics in a tropical forest and savanna of Central Africa

The forest–savanna transition zone is widely distributed on nutrient-poor oxisols in Central Africa. To reveal and compare the nutrient cycle in relation to soil microbes for forest and savanna vegetation in this area, we evaluated seasonal fluctuations in microbial biomass carbon (MBC), nitrogen (MBN), and phosphorus (MBP) for 13 months as well as soil moisture, temperature, soil pH levels, and nutrients for both vegetation types in eastern Cameroon. Soil pH was significantly lower in forest (4.3) than in savanna (5.6), and soil N availability was greater in forest (87.1 mg N kg⁻¹ soil) than in savanna (32.9 mg N kg⁻¹ soil). We found a significant positive correlation between soil moisture and MBP in forest, indicating the importance of organic P mineralization for MBP, whereas in savanna, we found a significant positive correlation between soil N availability and MBP, indicating N limitation for MBP. These results suggest that for soil microbes, forest is an N-saturated and P-limited ecosystem, whereas savanna is an N-limited ecosystem. Additionally, we observed a significantly lower MBN and larger MB C:N ratio in forest (50.7 mg N kg⁻¹ soil and 8.6, respectively) than in savanna (60.0 mg N kg⁻¹ soil and 6.5, respectively) during the experimental period, despite the rich soil N condition in forest. This may be due to the significantly lower soil pH in forest, which influences the different soil microbial communities (fungi-to-bacteria ratio) in forest versus savanna, and therefore, our results indicate that, in terms of microbial N dynamics, soil pH rather than soil substrate conditions controls the soil microbial communities in this area. Further studies should be focused on soil microbial community, such as PLFA, which was not evaluated in the present study.     

Microbial synthesis of organic and condensed forms of phosphorus in acid and calcareous soils

The potential for microorganisms to affect the quantity and quality of organic and condensed forms of phosphorus (P) in soils was investigated by repeated addition of different carbon sources (glucose, starch, cellulose; 2.5 g C kg^?1) with or without inorganic P (50 mg P kg^?1) to acid and calcareous soils which were either natural soils or clay–sand mixtures free of organic matter. Forms of P after five amendments and subsequent incubation periods of 5 weeks each were analyzed by ³¹P solution nuclear magnetic resonance (NMR) spectroscopy, and the microbial community composition was assessed by selective plate counts and fatty acid methyl ester (FAME) analysis. All carbon additions induced a redistribution of P from inorganic to organic and condensed forms, which was only little affected by the addition of inorganic P. Compared to non-carbon-amended controls, the greatest increase (7–38 mg P kg^?1) in organic P was observed in the monoester region. In the acid clay–sand mixture, there was a large accumulation of pyrophosphate (101 mg P kg^?1) after glucose addition and smaller accumulations (6–25 mg P kg^?1) after addition of starch and cellulose. Carbon additions increased the microbial biomass in all cases and except in the natural calcareous soil also the proportion of fungi. Redundancy analysis with Monte Carlo permutation tests revealed that for carbon-amended soils, the microbial community composition was more strongly influenced by soil type than by carbon source. Pyrophosphate was positively related to fungi, and diester P was positively related to soil pH. A large proportion of organic and condensed forms of P may still have been in microbial cells at the time of extraction. We have shown that soil organic P consists of some discrete and simple compounds along with some more complex forms, and that organic P recently synthesized by microbes consists almost exclusively of and thus is a likely source for the simple compounds found in natural soils.     

Stability of soil organic matter under long-term biosolids application

Little is know on the impact of biosolids application on soil organic matter (SOM) stability, which contributes to soil C sequestration. Soil samples were collected in 2006 at plow layer from fields that received liquid and dry municipal biosolids application from 1972 to 2004 at the cumulative rate of 1416 Mg ha⁻¹ in mined soil and 1072 Mg ha⁻¹ in nonmined soil and control fields that received chemical fertilizer at Fulton County, western Illinois. The biosolids application increased the soil microbial biomass C (SMBC) by 5-fold in mined soil and 4-fold in nonmined soil. The biosolids-amended soils showed a high amount of basal respiration and N mineralization, but low metabolic quotient, and low rate of organic C and organic N mineralization. There was a remarkable increase in mineral-associated organic C from 6.9 g kg⁻¹ (fertilizer control) to 26.6 g kg⁻¹ (biosolids-amended) in mined soil and from 8.9 g kg⁻¹ (fertilizer control) to 23.1 g kg⁻¹ (biosolids-amended) in nonmined soil. The amorphous Fe and Al, which can improve SOM stability, were increased by 2–7 folds by the long-term biosolids application. It is evident from this study that the biosolids-modified SOM resists to decomposition more than that in the fertilizer treatment, thus long-term biosolids application could increase SOM stability.     

Quadratic response models for N and P mineralization in domestic sewage sludge for mininig dump reclamation

A valuable feature of sewage sludge used for restoring degraded soils is its supplying capacity for C, N and P. A series of laboratory incubation experiments to quantify the release of N and P from raw (dried) and co-composted urban sewage sludges applied to mine dump soil were conducted. The effect of application dose (0–100 g kg⁻¹) and incubation time (0–30 day) on N and P mineralization as well as the process modelling were carried out by Response Surface Methodology. Models fitted revealed significant interaction effects between factors involved in soil-sludge dynamics, which accounted for 26% total variance in N-mineralization. The response models were used to predict nutrient releases required in properly formulating sludge management guidelines, viz. maximum simultaneous value for extractable inorganic forms of N and P achieved 11 and 18 days after applying 100 g kg⁻¹ of co-compost and dried sludge, respectively. Addition of sludges resulted into mineralization of 18% total N and up to 15% total P, while chemical and biochemical properties of the amended soil were improved paralleling organic matter mineralization. Compared to dried sludge, co-composting sludge lead to a decline of up to 30% and 65% in the availability in soil of N and P, respectively, but at expenses of C losses of only 7%, illustrating that co-composting was superior in turning sludge into an environmentally safe soil amendment.     

Phosphate additions have no effect on microbial biomass and activity in a northern hardwood forest

High rates of atmospheric nitrogen (N) deposition have raised questions about shifting patterns of nutrient limitation in northern hardwood forests. Of particular interest is the idea that increased supply of N may induce phosphorus (P) limitation of plant and microbial processes, especially in acid soils where P sorption by Al is high. In this study, we established field plots and plant-free laboratory mesocosms with P and Ca additions to test the hypotheses that 1) microbial biomass and activity are limited by P in the northern hardwood forest soils at the Hubbard Brook Experimental Forest in NH USA; 2) elevated Ca increases inherent P availability and therefore reduces any effects of added P and 3) P effects are more marked in the more carbon (C) rich Oie compared to the Oa horizon. Treatments included P addition (50 kg P ha⁻¹), Ca addition (850 kg Ca ha⁻¹) and Ca + P addition (850 kg Ca ha⁻¹ and 50 kg P ha⁻¹). The P treatments increased resin-available P levels and reduced phosphatase activity, but had no effect on microbial biomass C, microbial respiration, C metabolizing enzymes, potential net N mineralization and nitrification in the Oie or Oa horizon of either field plots or plant free mesocosms, in either the presence or absence of Ca. Total, prokaryote, and eukaryote PLFA were reduced by P addition, possibly due to reductions in mycorrhizal fungal biomass. These results suggest that increased N deposition and acidification have not created P limitation of microbial biomass and activity in these soils.     

Long-term effects of land use and fertiliser treatments on sulphur transformations in soils from the Broadbalk experiment

Sulphur transformations were monitored in a unique set of arable, grassland and woodland soils from the Broadbalk Classical Experiment, which started in 1843. In an open incubation experiment with periodic leaching, 14–35 mg SO₄²⁻-S kg⁻¹ was mineralised in 28 weeks at 25°C, equivalent to 4.4–8.3% soil organic S. Cumulative amounts of S mineralised increased linearly during the 28 weeks, indicating constant rates of mineralisation. The rate of mineralisation was the greatest in the woodland soil (170 μg SO₄-S kg⁻¹ day⁻¹), followed by the grassland (120 μg SO₄-S kg⁻¹ day⁻¹) and the arable soil from the farmyard manure (FYM) plot (110 μg SO₄-S kg⁻¹ day⁻¹). Three soils from arable plots receiving different inorganic fertiliser treatments but no FYM had similar rates of S mineralisation (~70 μg SO₄-S kg⁻¹ day⁻¹). In an incubation experiment with ³⁵SO₄²⁻, addition of glucose greatly enhanced S immobilisation. In 132 days, the woodland and grassland soils immobilised more S than the arable soils, with or without glucose amendment. Immobilisation and mineralisation of S occurred concurrently, and both were stimulated by glucose addition. The results show that S mineralisation and immobilisation were influenced strongly by the type of land-use and long-term organic manuring, whereas annual application of sulphate-containing fertilisers for over 150 years had few effects on short-term S transformations.     

Addition of organic and inorganic P sources to soil – Effects on P pools and microorganisms

Phosphorus deficiency is wide-spread due to the poor solubility of soil P and the rapid formation of poorly available P after P addition. Microbes play a key role in soil P dynamics by P uptake, solubilisation and mineralisation. Therefore a better understanding of the relationship between type of P amendment, microbial activity and changes in soil P pools is important for a better management of soil P. A P deficient soil was amended with two composts (low P or high P), two crop residues (low P or high P), and inorganic P (KH₂PO₄) at low and high P, and incubated for 56 days. Composts were added at 20 g kg⁻¹ resulting in a total P addition of 4.1 mg kg⁻¹ soil with the low P compost and 33.2 mg kg⁻¹ soil with the high P compost. The same amount of P was added with the other amendments (residues and inorganic P). All amendments increased cumulative respiration, but microbial biomass and the abundance of bacteria and fungi (assessed by phospholipid fatty acid analysis) increased significantly only in soils with organic amendments, with greater increases with residues. The concentration of the inorganic P pools NaHCO₃-P_i, NaOH-P_i and HCl-P increased significantly within 5 h after amendment, particularly with high P amendments. Over the following 56 days, labile inorganic P was converted mainly into non-labile inorganic P with inorganic P addition whereas labile and non-labile organic P was formed with organic amendments. It is concluded that organic P sources, particularly those with high P concentration can stimulate the formation of organic P forms in soils which may provide a long-term slow release P source for plants and soil organisms.     

Rapid estimation of microbial biomass in grassland soils by ultra-violet absorbance

A reliable and simple technique for estimating soil microbial biomass (SMB) is essential if the role of microbes in many soil processes is to be quantified. Conventional techniques are notoriously time-consuming and unreproducible. A technique was investigated that uses the UV absorbance at 280 nm of 0.5 M K₂SO₄ extracts of fumigated and unfumigated soils to estimate the concentrations of carbon, nitrogen and phosphorus in the SMB. The procedure is based on the fact that compounds released after chloroform fumigation from lysed microbial cells absorb in the near UV region. Using 29 UK permanent grassland soils, with a wide range of organic matter (2.9–8.0%) and clay contents (22–68%), it was demonstrated that the increase in UV absorbance at 280 nm after soil fumigation was strongly correlated with the SMB C (r=0.92), SMB N (r=0.90) and SMB P (r=0.89), as determined by conventional methods. The soils contained a wide range of SMB C (412–3412 μg g⁻¹ dry soil), N (57–346 μg g⁻¹ dry soil) and P (31–239 μg g⁻¹ dry soil) concentrations. It was thus confirmed that the UV absorbance technique described was a rapid, simple, precise and relatively inexpensive method of estimating soil microbial biomass.     

Soil available phosphorus status determines indigenous mycorrhizal colonization of field and glasshouse-grown spring wheat from Argentina

Wheat production (Triticum aestivum L.) has increased across the world during last century with the intensification of agriculture. Phosphorus (P) fertilization is a common practice to improve wheat growth in Argentina. We investigate whether indigenous arbuscular mycorrhizal colonization (AMC) of hard red spring wheat is controlled by shoot P content (SPc) or by available soil P in an agricultural soil from the southeastern Argentine Pampas. In the field, AMC was monitored four times during two growing seasons of a conventional wheat crop. Treatments were: without P supply, annual supply of 11 and 22 kg P ha⁻¹ during the last 5 years, and 164 kg P ha⁻¹ applied once 5 years before the experiment. In the glasshouse, AMC was assessed three times in wheat growing in pots filled with the soil from unfertilized plots; treatments were: P (0 and 20 mg P pot⁻¹), and nitrogen (N) fertilization (0 and 150 mg N pot⁻¹). A range of soil P between 6 and 60 mg P kg⁻¹ was obtained and the AMC ranged from 1% to 67% of root length colonized under both field and glasshouse conditions. P supplied annually increased growth and SPc but decreased AMC. N fertilization did not affect growth or AMC. Variations in SPc did not account for AMC. Variability in AMC was best accounted for local current soil available P content (r² = 0.59). A linear-plateau relationship between soil P and indigenous AMC was established in wheat plants growing under contrasting environmental and experimental (field and glasshouse) conditions. Indigenous AMC was depressed by available soil P in the range 0–27 mg P kg⁻¹ (a decrease of 2.8% mg P⁻¹ kg⁻¹). Above 27 mg P kg soil⁻¹, AMC was stabilized at about 10%. Grain yield increased with fertilization and the highest relative shoot dry matter in field was obtained at 15.5 mg P kg soil⁻¹. The soil P range that ensures high wheat production without deterring indigenous AMC is discussed.     

N2O emissions from humid tropical agricultural soils: effects of soil moisture,texture and nitrogen availability

We studied soil moisture dynamics and nitrous oxide (N₂O) fluxes from agricultural soils in the humid tropics of Costa Rica. Using a split-plot design on two soils (clay, loam) we compared two crop types (annual, perennial) each unfertilized and fertilized. Both soils are of andic origin. Their properties include relatively low bulk density and high organic matter content, water retention capacity, and hydraulic conductivity. The top 2–3 cm of the soils consists of distinct small aggregates (dia. <0.5 cm). We measured a strong gradient of bulk density and moisture within the top 7 cm of the clay soil. Using automated sampling and analysis systems we measured N₂O emissions at 4.6 h intervals, meteorological variables, soil moisture, and temperature at 0.5 h intervals. Mean daily soil moisture content at 5 cm depth ranged from 46% water filled pore space (WFPS) on clay in April 1995 to near saturation on loam during a wet period in February 1996. On both soils the aggregated surface layer always remained unsaturated. Soils emitted N₂O throughout the year. Mean N₂O fluxes were 1.04±0.72 ng N₂O-N cm⁻² h⁻¹ (mean±standard deviation) from unfertilized loam under annual crops compared to 3.54±4.31 ng N₂O-N cm⁻² h⁻¹ from the fertilized plot (351 days measurement). Fertilization dominated the temporal variation of N₂O emissions. Generally fluxes peaked shortly after fertilization and were increased for up to 6 weeks (‘post fertilization flux’). Emissions continued at a lower rate (‘background flux’) after fertilization effects faded. Mean post-fertilization fluxes were 6.3±6.5 ng N₂O-N cm⁻² h⁻¹ while the background flux rate was 2.2±1.8 ng N₂O-N cm⁻² h⁻¹. Soil moisture dynamics affected N₂O emissions. Post fertilization fluxes were highest from wet soils; fluxes from relatively dry soils increased only after rain events. N₂O emissions were weakly affected by soil moisture during phases of low N availability. Statistical modeling confirmed N availability and soil moisture as the major controls on N₂O flux. Our data suggest that small-scale differences in soil structure and moisture content cause very different biogeochemical environments within the top 7 cm of soils, which is important for net N₂O fluxes from soils.     

Organic waste amendment effects on soil microbial activity in a corn–rye rotation: Application of a new approach to community-level physiological profiling

The role of phosphorus (P) application and arbuscular mycorrhizal fungi (AMF) on growth, arsenic (As) and P accumulation in lettuce plants growing in an As-polluted soil (total As 250 mg kg⁻¹), was investigated. In particular, it was tested whether application of a commercial inoculum (CI), with (+P at 90 kg P ha⁻¹) and without (−P at 0 kg P ha⁻¹) P fertilizer, supported greater plant growth and provided more P, enhancing As tolerance, than indigenous fungi alone. The influence of these treatments on As and P availability in the rhizosphere and bulk soils was also investigated. Greenhouse pot experiments were established where plants were grown with and without commercial inoculum (+CI, −CI) in unsterilized conditions. Inoculation with commercial inoculum and P application together considerably increased plant biomass, by enhancing host plant P nutrition and lowering shoot and root As concentrations compared to plants inoculated only with native AMF. In the rhizosphere of +CI+P plants there was P soil depletion compared to −CI+P. The results evidenced that, with P addition, inoculation with commercial inoculum alleviated the toxicity of excessive As by improving P nutrition without increasing As concentrations in the plant, emphasizing the role of beneficial microbes and P fertilizer to improve soil fertility in As-contaminated soil.     

Effects of carbon and phosphorus addition on microbial respiration,N<Subscript>2</Subscript>O emission,and gross nitrogen mineralization in a phosphorus-limited grassland soil

Soil microbes are frequently limited by carbon (C), but also have a high phosphorus (P) requirement. Little is known about the effect of P availability relative to the availability of C on soil microbial activity. In two separate experiments, we assessed the effect of P addition (20 mg P kg^?1 soil) with and without glucose addition (500 mg C kg^?1 soil) on gross nitrogen (N) mineralization (¹⁵N pool dilution method), microbial respiration, and nitrous oxide (N₂O) emission in a grassland soil. In the first experiment, soils were incubated for 13 days at 90% water holding capacity (WHC) with addition of NO₃^? (99 mg N kg^?1 soil) to support denitrification. Addition of C and P had no effect on gross N mineralization. Initially, N₂O emission significantly increased with glucose, but it decreased at later stages of the incubation, suggesting a shift from C to NO₃^? limitation of denitrifiers. P addition increased the N₂O/CO₂ ratio without glucose but decreased it with glucose addition. Furthermore, the ¹⁵N recovery was lowest with glucose and without P addition, suggesting a glucose by P interaction on the denitrifying community. In the second experiment, soils were incubated for 2 days at 75% WHC without N addition. Glucose addition increased soil ¹⁵N recovery, but had no effect on gross N mineralization. Possibly, glucose addition increased short-term microbial N immobilization, thereby reducing N-substrates for nitrification and denitrification under more aerobic conditions. Our results indicate that both C and P affect N transformations in this grassland soil.     

Effects of cultivation on soil microbiological properties in a freshwater marsh soil in Northeast China

The Sanjiang Plain has become an intensive area of land use/cover change in China. However, little is known about the effect of cultivation on soil microbiological properties in this freshwater marsh ecosystem. Our objective was to evaluate the effect of cultivation on mineralizable, microbial biomass, and total C in the Sanjiang Plain of Northeast China. Soil microbial biomass C (MBC) was 4346 ± 309 mg kg⁻¹ in undisturbed marsh and 229 mg kg⁻¹ in soil cultivated for 15 years. Undisturbed marsh soil had the highest microbial quotient (3.64%), which declined with increasing cultivation time (R² = 0.97, p < 0.01). Metabolic quotient increased with increasing cultivation time. Soil C mineralization in undisturbed marsh was 3.5 times that in soil cultivated for 1 year, and was 12 times that in soil cultivated for 15 years. Cultivation strongly affected measured soil microbiological properties.     

Changing microbial substrate use in Arctic tundra soils through a freeze-thaw cycle

Recent research has established that microbial processes in the arctic continue even when soils are frozen, and that cold-season processes can be important in the overall annual carbon and nitrogen cycles. Despite the importance of wintertime soil microbial processes, our understanding of their controls remains extremely poor. We particularly have a poor understanding of how microbial substrate use patterns change as soils freeze: do microbes use the same substrates as during the growing season, only slower, or do they switch to using different substrates? We used a ¹⁴C isotope equilibration technique to partition respiration between the actively turning over microbial biomass and products pool and the plant detritus pool in a range of Arctic tundra soils. Microbes showed a step-function shift in their metabolism as soils cool from +2 to +0.5 °C, roughly doubling the contribution of recycling of microbial C to total soil respiration. There was no additional shift in substrate use as soils underwent bulk soil freezing. The above-0 °C substrate shift is important because tundra soils spend a long time at or just below 0 °C as they are freezing in the early winter. The change in substrate use represents a shift from processing N-poor detritus to N-rich microbial products, causing N available for either plant uptake or leaching to be greatest when soils are near 0 °C. This may explain the observed patterns of growing season N immobilization vs. cold-season mineralization that appear common in Arctic tundra ecosystems.     

Carbon mineralization and properties of water-extractable organic carbon in soils of the south Loess Plateau in China

Addition of organic manure over thousands of years has resulted in the development of very fertile soils in parts of the Loess Plateau in Northwest China. This region also suffers from serious soil erosion. For that reason, afforestation of arable soils has taken place. The dynamics of soil organic matter in these soils affected by a very specific management and by land use changes is largely unknown. Therefore, we measured C mineralization in a 35-days incubation experiment and analyzed amounts and properties of water-extractable organic carbon (WEOC) in 12 topsoils of this region. The soils differed in land use (arable vs. forest) and in amounts of added organic manure. Afforestation of arable soils resulted in a distinct stabilization of organic C as indicated by the smallest C mineralization (0.48 mg C g⁻¹ C d⁻¹) and the highest C content (2.3%) of the studied soils. In the soils exposed to intensive crop production without regular addition of organic manure we found the largest C mineralization (0.85 mg C g⁻¹ C d⁻¹) and the lowest contents of organic C (0.9%). Addition of organic manure over a time scale of millennia resulted in high organic C contents (1.8%) and small C mineralization (0.55 mg C g⁻¹ C d⁻¹). The content of WEOC reflected differences in C mineralization between the soils quite well and the two variables correlated significantly. Water-extractable organic C decreased during C mineralization from the soil illustrating its mainly labile character. Carbon mineralization from soils was particularly large in soils with small specific UV absorbance of WEOC. We conclude that amounts and properties of WEOC reflected differences in the stability of soil organic C. Both afforestation of arable land and the long-term addition of organic manure may contribute to C accumulation and stabilization in these soils.     

Microbial utilization and mineralization of [14C]glucose added in six orders of concentration to soil

The substrate availability for microbial biomass (MB) in soil is crucial for microbial biomass activity. Due to the fast microbial decomposition and the permanent production of easily available substrates in the rooted top soil mainly by plants during photosynthesis, easily available substrates make a very important contribution to many soil processes including soil organic matter turnover, microbial growth and maintenance, aggregate stabilization, CO₂ efflux, etc. Naturally occurring concentrations of easily available substances are low, ranging from 0.1 μM in soils free of roots and plant residues to 80 mM in root cells. We investigated the effect of adding ¹⁴C-labelled glucose at concentrations spanning the 6 orders of magnitude naturally occurring concentrations on glucose uptake and mineralization by microbial biomass. A positive correlation between the amount of added glucose and its portion mineralized to CO₂ was observed: After 22 days, from 26% to 44% of the added 0.0009 to 257 μg glucose C g^?1 soil was mineralized. The dependence of glucose mineralization on its amount can be described with two functions. Up to 2.6 μg glucose C g^?1 soil (corresponds to 0.78% of initial microbial biomass C), glucose mineralization increased with the slope of 1.8% more mineralized glucose C per 1 μg C added, accompanied by an increasing incorporation of glucose C into MB. An increased spatial contact between micro-organisms and glucose molecules with increasing concentration may be responsible for this fast increase in mineralization rates (at glucose additions <2.6 μg C g^?1). At glucose additions higher than 2.6 μg C g^?1 soil, however, the increase of the glucose mineralization per 1 μg added glucose was much smaller as at additions below 2.6 μg C g^?1 soil and was accompanied by decreasing portions of glucose ¹⁴C incorporated into microbial biomass. This supports the hypothesis of decreasing efficiency of glucose utilization by MB in response to increased substrate availability in the range 2.6–257 μg C g^?1 (=0.78–78% of microbial biomass C). At low glucose amounts, it was mainly stored in a chloroform-labile microbial pool, but not readily mineralized to CO₂. The addition of 257 μg glucose C g^?1 soil (0.78 μg C glucose μg^?1 C micro-organisms) caused a lag phase in mineralization of 19 h, indicating that glucose mineralization was not limited by the substrate availability but by the amount of MB which is typical for 2nd order kinetics.     

Enhancement of arbuscular mycorrhizal fungus (Glomus versiforme) on the growth and Cd uptake by Cd-hyperaccumulator Solanum nigrum

Arbuscular mycorrhizal fungus (AMF) can enhance plant growth and resistance to toxicity produced by heavy metals (HMs), affect the bioavailability of HMs in soil and the uptake of HMs by plants, and thus has been emerged as the most prominent symbiotic fungus for contribution to phytoremediation. A greenhouse pot experiment was conducted to assess the effect of Glomus versiforme BGC GD01C (Gv) on the growth and Cd accumulation of Cd-hyperaccumulator Solanum nigrum in different Cd-added soils (0, 25, 50, 100 mg Cd kg⁻¹ soil). Mycorrhizal colonization rates were generally high (from 71% to 82%) in Gv-inoculated treatments at all Cd levels. Gv colonization enhanced soil acid phosphatase activity, and hence elevated P acquisition and growth of S. nigrum at all Cd levels. Moreover, the presence of Gv significantly increased DTPA-extractable (phytoavailable) Cd concentrations in 25 and 50 mg Cd kg⁻¹ soils, but did not affect phytoavailable Cd in 100 mg Cd kg⁻¹ soil. Similarly, inoculation with Gv significantly increased Cd concentrations of S. nigrum in 25 and 50 mg Cd kg⁻¹ soils, but decreased Cd concentrations of the plants in 100 mg Cd kg⁻¹ soil. Overall, inoculation with Gv greatly improved the total Cd uptakes in all plant tissues at all Cd levels. The present results indicated that S. nigrum associated with Gv effectively improved the Cd uptake by plant and would be a new strategy in microbe-assisted phytoremediation for Cd-contaminated soils.     

Effect of freezing on soil nitrogen mineralization under different plant communities in a semi-arid area during a non-growing season

The influences of winter climate on terrestrial ecosystem processes have been the subject of growing attention, which is necessary to make the predictions about ecological responses to global warming in the future. However, little information can be found about the impacts of a large range of soil temperature fluctuation (e.g. −10 to 5 °C) over winter on the soil nitrogen (N) dynamics in the field. In the present study, we employed an intact soil core in situ incubation technique, and measured soil N mineralization and nitrification rates under three plant communities, i.e. a grassland, a shrub and a plantation, during the non-growing season (October 2004–April 2005) in Inner Mongolia, China. Our results demonstrate the significant effects of different plant communities on soil net N mineralization and the great temporal variations of soil N dynamics during the incubation period. The mean soil net N mineralization rates were 0.93, 0.77 and −1.28 mg N m⁻² d⁻¹, respectively, in the grassland, shrub and plantation. The mean soil NH₄⁺-N in the three plant communities declined by 40%, but the mean soil NO₃⁻-N increased by 190% by the end of the incubation compared with their initial concentrations at the beginning of incubation. The differences in plant communities significantly affected their soil N mineralization rates, accumulations and turnover rates, which followed the order: grassland > shrub > plantation. During the winter time, the studied soils experienced the three phases consisting of mild freezing (−7 to −2 °C soil), deep freezing (approximately −10 °C soil) and freeze–thaw (−2 to 5 °C soil). The results suggest that temporal variations of soil N mineralization are positively affected by the soil temperature and the soil nitrification is dominant in the N transformation process during the non-growing season. Our study indicates that the soil N mineralization over winter can make a substantial contribution to the mineral N pool that plants are able to utilize in the upcoming spring, but may also pose a great risk of mineral N leaching loss if great rainfalls occur during spring and early summer.     

Changes of microbial properties in (near-) rhizosphere soils after phytoextraction by Sedum alfredii H: A rhizobox approach with an artificial Cd-contaminated soil

The ultimate goal of soil remediation is to restore soil health. Soil microbial parameters are considered to be effective indicators of soil health. The aim of this study was to determine the effects of phytoextraction on microbial properties through the measurement of soil microbial biomass carbon, soil basal respiration and enzyme activities. For this purpose, a pre-stratified rhizobox experiment was conducted with the Cd hyperaccumulator Sedum alfredii H. for phytoextraction Cd from an artificial contaminated soil (15.81 mg kg⁻¹) under greenhouse conditions. The plant and soil samples were collected after growing the plant for three and six months with three replications. The results indicated that the ecotype of S. alfredii H. originating from an ancient silver mining site was a Cd-hyperaccumulator as it showed high tolerance to Cd stress, the shoot Cd concentration were as high as 922.6 mg kg⁻¹ and 581.9 mg kg⁻¹ at the two samplings, and it also showed high BF (58.4 and 36.8 after 3 and 6 months growth), and TF (5.8 and 5.1 after 3 and 6 months growth). The amounts of Cd accumulated in the shoots of S. alfredii reached to an average of 1206 μg plant⁻¹ after 6 months growth. Basal respiration, invertase and acid phosphatase activities of the rhizosphere soil separated by the shaking method were significantly higher (P < 0.01) than that of the near-rhizosphere soil and the unplanted soil after 3 months growth, so were microbial biomass carbon, urease, invertase and acid phosphatase activities of the rhizosphere soil after 6 months growth. Acid phosphatase activity of the 0–2 mm sub-layer rhizosphere soil collected by the pre-stratified method after 3 months growth was significantly higher (P < 0.05) than that of other sub-layer rhizosphere soils and bulk soil, and so were microbial biomass carbon, basal respiration, urease, invertase and acid phosphatase activities of the 0–2 mm sub-layer rhizosphere soil after 6 months growth. It was concluded that phytoextraction by S. alfredii could improve soil microbial properties, especially in rhizosphere, and this plant poses a great potential for the remediation of Cd contaminated soil.