Clinoptilolite zeolite and cellulose amendments to reduce ammonia volatilization in a calcareous sandy soil

Leaching of nitrate (NO₃ ^–) below the root zone and gaseous losses of nitrogen (N) such as ammonia (NH₃) volatilization, are major mechanisms of N loss from agricultural soils. New techniques to minimize such losses are needed to maximize N uptake efficiency and minimize production costs and the risk of potential N contamination of ground and surface waters. The effects of cellulose (C), clinoptilolite zeolite (CZ), or a combination of both (C+CZ) on NH₃ volatilization and N transformation in a calcareous Riviera fine sand (loamy, siliceous, hyperthermic, Arenic Glossaqualf) from a citrus grove were investigated in a laboratory incubation study. Ammonia volatilization from NH₄NO₃ (AN), (NH₄)₂SO₄(AS), and urea (U) applied at 200 mg N kg^–1 soil decreased by 2.5-, 2.1- and 0.9-fold, respectively, with cellulose application at 15 g kg^–1 and by 4.4-, 2.9- and 3.0-fold, respectively, with CZ application at 15 g kg^–1 as compared with that from the respective sources without the amendments. Application of cellulose plus CZ (each at 15 g kg^–1) was the most effective in decreasing NH₃ volatilization. Application of cellulose increased the microbial biomass, which was responsible for immobilization of N, and thus decreased volatilization loss of NH₃–N. The effect of CZ, on the other hand, may be due to increased retention of NH₄ in the ion-exchange sites. The positive effect of interaction between cellulose and CZ amendment on microbial biomass was probably due to improved nutrient retention and availability to microorganisms in the soil. Thus, the amendments provide favorable conditions for microbial growth. These results indicate that soil amendment of CZ or CZ plus organic materials such as cellulose has great potential in reducing fertilizer N loss in sandy soils.     

Soil Carbon, Nitrogen and Phosphorus Dynamics as Affected by Solarization Alone or Combined with Organic Amendment

Soil solarization, alone or combined with organic amendment, is an increasingly attractive approach for managing soil-borne plant pathogens in agricultural soils. Even though it consists in a relatively mild heating treatment, the increased soil temperature may strongly affect soil microbial processes and nutrients dynamics. This study aimed to investigate the impact of solarization, either with or without addition of farmyard manure, in soil dynamics of various C, N and P pools. Changes in total C, N and P contents and in some functionally-related labile pools (soil microbial biomass C and N, K₂SO₄-extractable C and N, basal respiration, KCl-exchangeable ammonium and nitrate, and water-soluble P) were followed across a 72-day field soil solarization experiment carried out during a summer period on a clay loam soil in Southern Italy. Soil physico-chemical properties (temperature, moisture content and pH) were also monitored. The average soil temperature at 8-cm depth in solarized soils approached 55 °C as compared to 35 °C found in nonsolarized soil. Two-way ANOVA (solarization×organic amendment) showed that both factors significantly affected most of the above variables, being the highest influence exerted by the organic amendment. With no manure addition, solarization did not significantly affect soil total C, N and P pools. Whereas soil pH, microbial biomass and, at a greater extent, K₂SO₄-extractable N and KCl-exchangeable ammonium were greatly affected. An increased release of water-soluble P was also found in solarized soils. Yet, solarization altered the quality of soluble organic residues released in soil as it lowered the C-to-N ratio of both soil microbial biomass and K₂SO₄-extractable organic substrates. Additionally, in solarized soils the metabolic quotient (qCO₂) significantly increased while the microbial biomass C-to-total organic C ratio (microbial quotient) decreased over the whole time course. We argued that soil solarization promoted the mineralization of readily decomposable pools of the native soil organic matter (e.g. the microbial biomass) thus rendering larger, at least over a short-term, the available fraction of some soil mineral nutrients, namely N and P forms. However, over a longer prospective solarization may lead to an over-exploitation of labile organic resources in agricultural soils. Manure addition greatly increased the levels of both total and labile C, N and P pools. Thus, addition of organic amendments could represent an important strategy to protect agricultural lands from excessive soil resources exploitation and to maintain soil fertility while enhancing pest control.     

Microbial immobilization drives nitrogen cycling differences among plant species

In many terrestrial ecosystems nitrogen (N) limits productivity and plant community composition is influenced by N availability. However, vegetation is not only controlled by N; plant species may influence ecosystem N dynamics through positive or negative effects on N cycling. We examined four potential mechanisms of plant species effects on nitrogen (N) cycling. We found no species differences in gross ammonification suggesting there are no changes in the ecosystem N cycling rate between the soil organic matter pool (SOM) and the plant/microbial pool. We also found weak differences among plant species in gross nitrification, thus plant species only marginally change the relative sizes of the NH₄⁺ and NO₃^? pools. Next, more than 90% of mineralized N was microbially immobilized, and microbial N immobilization was positively correlated with root biomass. Finally, while species differed in extractable soil NO3^? concentration, these differences were not related to root biomass suggesting that microbial immobilization drives net N mineralization and soil NO₃^? levels. Our results indicate that plant species do not cause feedbacks on the N cycling rate among the three major ecosystem N pools over nine years. However, plant carbon (C) inputs to the soil control microbial N immobilization and thereby change N partitioning between the plant and microbial N pools. Furthermore our results suggest that the SOM pool can act as a strong bottleneck for N cycling in these systems.     

Nitrate influx kinetic parameters of five potato cultivars during vegetative growth

This study examines the effect of elevated CO₂ on short-term partitioning of inorganic N between a grass and soil micro-organisms. ¹⁵N-labelled NH₄⁺ was injected in the soil of mesocosms of Holcus lanatus (L.) that had been grown for more than 15 months at ambient or elevated CO₂ in reconstituted grassland soil. After 48 h, the percentage recovery of added ¹⁵N was increased in soil microbial biomass N at elevated CO₂, was unchanged in total plant N and was decreased in soil extractable N. However, plant N content and microbial biomass N were not significantly affected by elevated CO₂. These results and literature data from plant–microbial ¹⁵N partitioning experiments at elevated CO₂ suggest that the mechanisms controlling the effects of CO₂ on short- vs. long-term N uptake and turnover differ. In particular, short-term immobilisation of added N by soil micro-organisms at elevated CO₂ does not appear to lead to long-term increases in N in soil microbial biomass. In addition, the increased soil microbial C:N ratios that we observed at elevated CO₂ suggest that long-term exposure to CO₂ alters either the functioning or structure of these microbial communities.     

Transformation of14C labelled plant components in soil in relation to immobilization and remineralization of15N fertilizer

Summary Uniformly¹⁴C labelled glucose, cellulose and wheat straw and specifically¹⁴C labelled lignin component in corn stalks were aerobically incubated for 12 weeks in a chernozem soil alongwith¹⁵N labelled ammonium sulphate. Glucose was most readily decomposed, followed in order by cellulose, wheat straw and corn stalk lignins labelled at methoxyl-, side chain 2-and ring-C. More than 50% of¹⁴C applied as glucose, cellulose and wheat straw evolved as CO₂ during the first week. Lignin however, decomposed relatively slowly. A higher proportion of¹⁴C was transformed into microbial biomass whereas lignins contributed a little to this fraction.After 12 weeks of incubation nearly 60% of the lignin¹⁴C was found in humic compounds of which more than 70% was resistant to hydrolysis with 6N HCl. Maximum incorporation of¹⁵N in humic compounds was observed in cellulose amended soil. However, in this case more than 80% of the¹⁵N was in hydrolysable forms.Immobilization-remineralization of applied¹⁵N was most rapid in glucose treated soil and a complete immobilization followed by remineralization was observed after 3 days. The process was much slow in soil treated with cellulose, wheat straw or corn stalks. More than 70% of the newly immobilized N was in hydrolysable forms mainly reepresenting the microbial component.Serial hydrolysis of soil at different incubation intervals showed a greater proportion of 6N HCl hydrolysable¹⁴C and¹⁵N in fractions representing microbial material.¹⁴C from lignin carbons was relatively more uniformly distributed in different fractions as compared to glucose, cellulose and wheat straw where a major portion of¹⁴C was in easily hydrolysable fractions.     

Microbes drive global soil nitrogen mineralization and availability

Soil net nitrogen mineralization rate (N_min), which is critical for soil nitrogen availability and plant growth, is thought to be primarily controlled by climate and soil physical and/or chemical properties. However, the role of microbes on regulating soil N_min has not been evaluated on the global scale. By compiling 1565 observational data points of potential net N_min from 198 published studies across terrestrial ecosystems, we found that N_min significantly increased with soil microbial biomass, total nitrogen, and mean annual precipitation, but decreased with soil pH. The variation of N_min was ascribed predominantly to soil microbial biomass on global and biome scales. Mean annual precipitation, soil pH, and total soil nitrogen significantly influenced N_min through soil microbes. The structural equation models (SEM) showed that soil substrates were the main factors controlling N_min when microbial biomass was excluded. Microbe became the primary driver when it was included in SEM analysis. SEM with soil microbial biomass improved the N_min prediction by 19% in comparison with that devoid of soil microbial biomass. The changes in N_min contributed the most to global soil NH₄⁺‐N variations in contrast to climate and soil properties. This study reveals the complex interactions of climate, soil properties, and microbes on N_min and highlights the importance of soil microbial biomass in determining N_min and nitrogen availability across the globe. The findings necessitate accurate representation of microbes in Earth system models to better predict nitrogen cycle under global change.     

Short-term nitrous oxide emissions from pasture soil as influenced by urea level and soil nitrate

Nitrogen excreted by cattle during grazing is a significant source of atmospheric nitrous oxide (N₂O). The regulation of N₂O emissions is not well understood, but may vary with urine composition and soil conditions. This laboratory study was undertaken to describe short-term effects on N₂O emissions and soil conditions, including microbial dynamics, of urea amendment at two different rates (22 and 43 g N m⁻²). The lower urea concentration was also combined with an elevated soil NO ₃ ⁻ concentration. Urea solutions labelled with 25 atom%¹⁵N were added to the surface of repacked pasture soil cores and incubated for 1, 3, 6 or 9 days under constant conditions (60% WFPS, 14 °C). Soil inorganic N (NH ₄ ⁺ , NO ₂ ⁻ and NO ₃ ⁻ ), pH, electrical conductivity and dissolved organic C were quantified. Microbial dynamics were followed by measurements of CO₂ evolution, by analyses of membrane lipid (PLFA) composition, and by measurement of potential ammonium oxidation and denitrifying enzyme activity. The total recovery of¹⁵N averaged 84%. Conversion of urea-N to NO ₃ ⁻ was evident, but nitrification was delayed at the highest urea concentration and was accompanied by an accumulation of NO ₂ ⁻ . Nitrous oxide emissions were also delayed at the highest urea amendment level, but accelerated towards the end of the study. The pH interacted with NH ₄ ⁺ to produce inhibitory concentrations of NH₃(aq) at the highest urea concentration, and there was evidence for transient negative effects of urea amendment on both nitrifying and denitrifying bacteria in this treatment. However, PLFA dynamics indicated that initial inhibitory effects were replaced by increased microbial activity and net growth. It is concluded that urea-N level has qualitative, as well as quantitative effects on soil N transformations in urine patches.     

Decomposition of14C- and15N-labeled organisms in soil under anaerobic conditions

Carbon and nitrogen mineralized from soil under waterlogged conditions may come from the soil microbial biomass pool and potentially could be used for biomass estimations.¹⁴C and¹⁵N labeled cells added to soil were monitored for decomposition under aerobic and anaerobic conditions. Under aerobic conditions 12–42% of the added organism C was mineralized and 1–30% of the N. Under waterlogged conditions 13–33% of the C and 4–13% of the N was mineralized. The mineralized organism C as a percent of the total C evolved was consistent for both aerobic and anaerobic conditions, however the nitrogen showed extreme variations     

Influence of light intensity on the distribution of carbon and consequent effects on mineralization of soil nitrogen in a barley (Hordeum vulgare L.)-soil system

A pot experiment was conducted in a ¹⁴C-labelled atmosphere to study the influence of living plants on organic-N mineralization. The soil organic matter had been labelled, by means of a 200-days incubation, with ¹⁵N. The influence of the carbon input from the roots on the formation of microbial biomass was evaluated by using two different light intensities (I). Mineralization of ¹⁵N-labelled soil N was examined by following its fate in both the soil biomass and the plants. Less dry matter accumulated in shoots and roots at the lower light intensity. Furthermore, in all the plant-soil compartments examined, with the exception of rhizosphere respiration, the proportion of net assimilated ¹⁴C was lower in the low-I treatment than in the high-I treatment. The lower rates of ¹⁴C and ¹⁵N incorporation into the soil biomass were associated with less root-derived ¹⁴C. During the chamber period (¹⁴CO₂-atmosphere), mineralized amounts of ¹⁵N (measured as plant uptake of ¹⁵N) were small and represented about 6.8 to 7.8% of the initial amount of organic ¹⁵N in the soil. Amounts of unlabelled N found in the plants, as a percentage of total soil N, were 2.5 to 3.3%. The low availability of labelled N to microorganisms was the result of its stabilization during the 210 days of soil incubation. Differences in carbon supply resulted in different rates of N mineralization which is consistent with the hypothesis that roots induce N mineralization. N mineralization was higher in the high-I treatment. On the other hand, the rate of mineralization of unlabelled stable soil N was lower than labelled soil ¹⁵N which was stabilized. The amounts of ¹⁵N mineralized in planted soil during the chamber period (43 days) which were comparable with those mineralized in unplanted soil incubated for 210 days, also suggested that living plants increased the turnover rate of soil organic matter.     

The fate of 15N added to high Arctic tundra to mimic increased inputs of atmospheric nitrogen released from a melting snowpack

Increases in the long‐range aerial transport of reactive N species from low to high latitudes will lead to increased accumulation in the Arctic snowpack, followed by release during the early summer thaw. We followed the release of simulated snowpack N, and its subsequent fate over three growing seasons, on two contrasting high Arctic tundra types on Spitsbergen (79°N). Applications of ¹⁵N (99 atom%) at 0.1 and 0.5 g N m^?2 were made immediately after snowmelt in 2001 as either Na¹⁵NO₃ or ¹⁵NH₄Cl. These applications are approximately 1 × and 5 × the yearly atmospheric deposition rates. The vegetation at the principal experimental site was dominated by bryophytes and Salix polaris while at the second site, vegetation included bryophytes, graminoids and lichens. Audits of the applied ¹⁵N were undertaken, over two or three growing seasons, by determining the amounts of labeled N in the soil (0–3 and 3–10 cm), soil microbial biomass and different vegetation fractions. Initial partitioning of the ¹⁵N at the first sampling time showed that ～60% of the applied ¹⁵N was recovered in soil, litter and plants, regardless of N form or application rate, indicating that rapid immobilization into organic forms had occurred at both sites. Substantial incorporation of the ¹⁵N was found in the microbial biomass in the humus layer and in the bryophyte and lichen fractions. After initial partitioning there appeared to be little change in the total ¹⁵N recovered over the following two or three seasons in each of the sampled fractions, indicating highly conservative N retention. The most obvious transfer of ¹⁵N, following assimilation, was from the microbial biomass into stable forms of humus, with an apparent half‐life of just over 1 year. At the principal site the microbial biomass and vascular plants were found to immobilize the greatest proportion of ¹⁵N compared with their total N concentration. In the more diverse tundra of the second site, lichen species and graminoids competed effectively for ¹⁵NH₄‐N and ¹⁵NO₃‐N, respectively. Results suggest that Arctic tundra habitats have a considerable capacity to immobilize additional inorganic N released from the snow pack. However, with 40% of the applied ¹⁵N apparently lost there is potential for N enrichment in the surrounding fjordal systems during the spring thaw.     

Rapid immobilization of applied nitrogen in saline–alkaline soils

The dynamics of inorganic N are important in soil, and this applies particularly to the saline–alkaline soils of the former lake Texcoco in Mexico with high pH and salinity where a forestation program was started in the 1970s. In soils of lake Texcoco, in Mexico, more than 50% of applied N could not be accounted for one day after application of 200 mg kg^–1 soil along with glucose amendment. It was not clear whether this was due to abiotic or biotic processes, the form of inorganic N applied or the result of applying an easily decomposable substrate. We investigated this by adding glucose and 200 mg kg^–1 soil as (NH₄)₂SO₄-N or KNO₃-N to sterilized and unsterilized soil. The changes in inorganic and ninhydrin N, microbial biomass C and production of CO₂ were then monitored. Between the time of applying N and extraction with 0.5 M K₂SO₄, i.e., after ca 2 h, approximately 110 mg NH₄ ⁺-N kg^–1 dry soil could not be accounted for in the unsterilized and sterilized soil and that remained so for the entire incubation in the sterilized soil. After 1 day this increased to 140 mg NH₄ ⁺-N kg^–1 dry soil in the unsterilized control and 170 mg NH₄ ⁺-N kg^–1 dry soil in C amended soil. Volatilization of NH₃ accounted for 56 mg NH₄ ⁺-N kg^–1 so the rest appeared to be adsorbed on the soil matrix. The NH₃ volatilization and NH₄ ⁺ fixed in the soil matrix remained constant over time and no oxidation to NO₂ ^– or NO₃ ^– had occurred, so unaccounted N in unsterilized soil was probably incorporated into the microbial biomass in excess of what was required for metabolic activity. The unaccounted N was ca 70 mg NO₃ ^––N in nitrate amended soil after 3 days and 138 NO₃ ^––N when glucose was additionally added. Losses through abiotic processes were absent as inferred from changes in sterilized soil and the aerobic incubation inhibited possible losses through denitrification. It was inferred that NO₃ ^– that could not be accounted for was taken up by micro-organisms in excess of what was required for metabolic activity.     

Patterns of restoration of soil physciochemical properties and microbial biomass in different landslide sites in the sal forest ecosystem of Nepal Himalaya

The pattern of natural restoration in soil components and processes was documented in five landslide-damaged (1–58-year-old) sites in the moist tropical sal (Shorea robusta) forest ecosystem of Nepal Himalaya. Comparisons were made with an undisturbed forest site in the same region. Concentrations of soil organic C, total N, total P and extractable nutrients (Ca, Mg and K) increased with the age of sites. The 58-year-old site showed concentrations of soil organic C, total N and total P that were 75–89% of concentrations in the undisturbed sal forest. The soil microbial biomass, the active fraction of soil organic matter, showed similar seasonal variations at all sites. The amount of mean microbial biomass (expressed as C, N and P contents) increased 4–5 times at the 58-year-old site relative to the 1-year-old site, and the bulk increase occurred within the initial 15 year. The increase in the C/N ratio of soil microbial biomass with age (9.4–11.6 years) reflected change in its composition. Although the net N-mineralization rate increased consistently until 58 years of age, the proportion of nitrification rate relative to ammonification rate distinctly decreased beyond 40 years. On the other hand, the soil available-N (both NO₃⁻ and NH₄⁺) concentrations increased from 1 to 40 year and then declined; with age the proportion of NH₄⁺ increased, however. Rates of restoration in soil properties were faster in the early successional stages (1–15 year) than late stages. Among different soil properties the restoration of soil microbial biomass (C and N) was faster than soil organic C and total N. Best fit power function models showed that the estimated times for the 58-year-old site to reach the level of the undisturbed, mature sal forest would be about 30–35 year for microbial biomass (C and N) and about 100–150 year for organic C and total N. Higher accumulation of soil microbial biomass and high N-mineralization rate at late successional stages indicated the re-establishment of enriched soil and restitution of nutrient cycling during the course of ecosystem restoration.     

Biochar Effectively Reduces Ammonia Volatilization From Nitrogen-Applied Soils in Tea and Bamboo Plantations

Intensive practices in forest soils result in dramatic nitrogen (N) losses, particularly ammonia (NH₃) volatilization, to adjacent environmental areas. A soil column experiment was conducted to evaluate the effect of bamboo biochar on NH₃ volatilization from tea garden and bamboo forest soils. The results showed that biochar amendment effectively reduced NH₃ volatilization from tea garden and bamboo forest soil by 79.2% and 75.5%, respectively. The soil pH values increased by 0.53-0.61 units after biochar application. The NH₄⁺-N and total N of both soils were 13.8-29.7% and 34.0-41.9% higher under the biochar treatments than under the control treatment, respectively. In addition, the soil water contents of the two biochar-amended soils were significantly higher (P < 0.05), by 10.7-12.5%, than that of the soils without biochar amendment. Therefore, biochar mitigates NH₃ volatilization from the tested forest soils, which was due to the increases in soil NH₄⁺-N, total N and water contents after biochar amendment. Our main findings suggest that biochar addition is an effective management option for sustainable forest management.     

Low sedimentary accumulation of lead caused by weak downward export of organic matter in Hudson Bay,northern Canada

Subtropical forests receive increasing amounts of atmogenic nitrogen (N), both as ammonium (NH₄ ⁺) and nitrate (NO₃ ^?). Previous long-term studies indicate efficient turnover of atmogenic NH₄ ⁺ to NO₃ ^? in weathered, acidic soils of the subtropics, leading to excessive NO₃ ^? leaching. To clarify the mechanism governing the fate of atmogenic inputs in these soils, we conducted an in situ ¹⁵N tracing experiment in the TieShanPing (TSP) forested catchment, SW China. ¹⁵NH₄NO₃, NH ₄ ¹⁵ NO₃ and ¹⁵N-glutamic acid were applied to an upland hillslope soil and inorganic N, total soil N and nitrous oxide (N₂O) were monitored for nine days. Incorporation of ¹⁵NO₃ ^? into soil organic N was negligible and 80% of the applied label was lost from the top soil (0–15 cm) primarily by leaching within 9 days. In contrast, ¹⁵NH₄ ⁺ was largely retained in soil organic N. However, instant production of ¹⁵NO₃ ^? in the ¹⁵NH₄ ⁺ treatment suggested active nitrification. In both the ¹⁵NH₄ ⁺ and ¹⁵N-glutamic acid treatments, the ¹⁵N enrichment in the NO₃ ^? pool exceeded that in the NH₄ ⁺ pool one day after ¹⁵N application, suggesting preferential nitrification of added ¹⁵NH₄ ⁺ with subsequent dilution of the NH₄ ⁺ pool and/or immobilization of ¹⁵NH₄ ⁺ followed by heterotrophic nitrification. The cumulative recovery of ¹⁵N in N₂O after 9 days ranged from 2.5 to 6.0% in the ¹⁵NO₃ ^? treatment, confirming the previously reported significant response of N₂O emission to N deposition. Source partitioning of ¹⁵N₂O demonstrated a measurable contribution of nitrification to N₂O emissions, particularly at low soil moistures. Our study emphasizes the role of a fast-cycling organic N pool (including microbial N) for retention and transformation of atmogenic NH₄ ⁺ in subtropical, acid forest soils. Thus, it explains the near-quantitative leaching of deposited N (as NO₃ ^? and NH₄ ⁺) common to subtropical forest soils with chronic, elevated atmogenic N inputs by (i) negligible retention of NO₃ ^? in the soil and (ii) rapid immobilization-mineralization of NH₄ ⁺ followed by nitrification. Our findings point to a leaky N cycle in N-saturated Chinese subtropical forests with consequences for regional soil acidification, N pollution of fresh waters and N₂O emission.     

Pulse additions of soil carbon and nitrogen affect soil nitrogen dynamics in an arid Colorado Plateau shrubland

Biogeochemical cycles in arid and semi-arid ecosystems depend upon the ability of soil microbes to use pulses of resources. Brief periods of high activity generally occur after precipitation events that provide access to energy and nutrients (carbon and nitrogen) for soil organisms. To better understand pulse-driven dynamics of microbial soil nitrogen (N) cycling in an arid Colorado Plateau ecosystem, we simulated a pulsed addition of labile carbon (C) and N in the field under the canopies of the major plant species in plant interspaces. Soil microbial activity and N cycling responded positively to added C while NH₄⁺–N additions resulted in an accumulation of soil NO₃⁻. Increases in microbial activity were reflected in higher rates of respiration and N immobilization with C addition. When both C and N were added to soils, N losses via NH₃ volatilization decreased. There was no effect of soil C or N availability on microbial biomass N suggesting that the level of microbial activity (respiration) may be more important than population size (biomass) in controlling short-term dynamics of inorganic and labile organic N. The effects of C and N pulses on soil microbial function and pools of NH₄⁺–N and labile organic N were observed to last only for the duration of the moisture pulse created by treatment addition, while the effect on the NO₃⁻–N pool persisted after soils dried to pre-pulse moisture levels. We observed that increases in available C lead to greater ecosystem immobilization and retention of N in soil microbial biomass and also lowered rates of gaseous N loss. With the exception of trace gas N losses, the lack of interaction between available C and N on controlling N dynamics, and the subsequent reduction in plant available N with C addition has implications for the competitive relationships between plants species, plants and microbes, or both.     

Impacts of urea N addition on soil microbial community in a semi-arid temperate steppe in northern China

Nitrogen (N) addition has been well documented to decrease plant biodiversity across various terrestrial ecosystems. However, such generalizations about the impacts of N addition on soil microbial communities are lacking. This study was conducted to examine the impacts of N addition (urea-N fertilizer) on soil microbial communities in a semi-arid temperate steppe in northern China. Soil microbial biomass carbon (C), biomass N (MBN), net N mineralization and nitrification, and bacterial and fungal community level physiological profiles (CLPP) along an N addition gradient (0–64 g N m^?2 year^?1) were measured. Three years of N addition caused gradual or step increases in soil NH₄-N, NO₃-N, net N mineralization and nitrification in the early growing season. The reductions in microbial biomass under high N addition levels (32 and 64 g N m^?2 year^?1) are partly attributed to the deleterious effects of soil pH. An N optimum between 16 and 32 g N m^?2 year^?1 in microbial biomass and functional diversity exists in the temperate steppe in northern China. Similar N loading thresholds may also occur in other ecosystems, which help to interpret the contrasting observations of microbial responses to N addition.     

Microbial transformations of C and N in a boreal forest floor as affected by temperature

The effects of temperature on N mineralization were studied in two organic surface horizons (LF and H) of soil from a boreal forest. The soil was incubated at 5 °C and 15 °C after adding ¹⁵ N and gross N fluxes were calculated using a numerical simulation model. The model was calibrated on microbial C and N, basal respiration, and KCl-extractable NH₄ ⁺, NO₃ ⁻, ¹⁵NH₄ ⁺ and ¹⁵ NO₃ ⁻. In the LF layer, increased temperature resulted in a faster turnover of all N pools. In both layers net N mineralization did not increase at elevated temperature because both gross NH₄ ⁺ mineralization and NH₄ ⁺ immobilization increased. In the H layer, however, both gross NH₄ ⁺ mineralization and NH₄ ⁺ immobilization were lower at 15 °C than at 5 °C and the model predicted a decrease in microbial turnover rate at higher temperature although measured microbial activity was higher. The decrease in gross N fluxes in spite of increased microbial activity in the H layer at elevated temperature may have been caused by uptake of organic N. The model predicted a decrease in pool size of labile organic matter and microbial biomass at elevated temperature whereas the amount of refractory organic matter increased. Temperature averaged microbial C/N ratio was 14.7 in the LF layer suggesting a fungi-dominated decomposer community whereas it was 7.3 in the H layer, probably due to predominance of bacteria. Respiration and microbial C were difficult to fit using the model if the microbial C/N ratio was kept constant with time. A separate ¹⁵N-enrichment study with the addition of glucose showed that glucose was metabolized faster in the LF than in the H layer. In both layers, decomposition of organic matter appeared to be limited by C availability. This revised version was published online in June 2006 with corrections to the Cover Date.     

A meta‐analysis of soil salinization effects on nitrogen pools,cycles and fluxes in coastal ecosystems

Salinity intrusion caused by land subsidence resulting from increasing groundwater abstraction, decreasing river sediment loads and increasing sea level because of climate change has caused widespread soil salinization in coastal ecosystems. Soil salinization may greatly alter nitrogen (N) cycling in coastal ecosystems. However, a comprehensive understanding of the effects of soil salinization on ecosystem N pools, cycling processes and fluxes is not available for coastal ecosystems. Therefore, we compiled data from 551 observations from 21 peer‐reviewed papers and conducted a meta‐analysis of experimental soil salinization effects on 19 variables related to N pools, cycling processes and fluxes in coastal ecosystems. Our results showed that the effects of soil salinization varied across different ecosystem types and salinity levels. Soil salinization increased plant N content (18%), soil NH₄⁺ (12%) and soil total N (210%), although it decreased soil NO₃^? (2%) and soil microbial biomass N (74%). Increasing soil salinity stimulated soil N₂O fluxes as well as hydrological NH₄⁺ and NO₂^? fluxes more than threefold, although it decreased the hydrological dissolved organic nitrogen (DON) flux (59%). Soil salinization also increased the net N mineralization by 70%, although salinization effects were not observed on the net nitrification, denitrification and dissimilatory nitrate reduction to ammonium in this meta‐analysis. Overall, this meta‐analysis improves our understanding of the responses of ecosystem N cycling to soil salinization, identifies knowledge gaps and highlights the urgent need for studies on the effects of soil salinization on coastal agro‐ecosystem and microbial N immobilization. Additional increases in knowledge are critical for designing sustainable adaptation measures to the predicted intrusion of salinity intrusion so that the productivity of coastal agro‐ecosystems can be maintained or improved and the N losses and pollution of the natural environment can be minimized.     

The fate of15N enriched throughfall in two coniferous forest stands at different nitrogen deposition levels

The stable isotope¹⁵N was added as (¹⁵NH₄)₂SO₄ to throughfall water for one year, to study the fate of the deposited nitrogen at different levels of N deposition in two N saturated coniferous forests ecosystems in the Netherlands. The fate of the¹⁵N was followed at high-N (44–55 kg N ha^–1 yr^–1) 1) and low-N (4–6 kg N ha^–1 yr^–1) deposition in plots established under transparent roofs build under the canopy in a Douglas fir (Pseudotsuga menziesii (Mirb.) Franco.) and Scots pine (Pinus sylvestris L.) forest.The applied¹⁵N was detectable in needles and twigs, the soil and soil water leaching below the rooting zone (90 cm depth). Total¹⁵N recovery in major ecosystem compartments was 71–100% during two successive growing seasons after the start of a year-round¹⁵N application to throughfall-N. Nine months after the year-round¹⁵N application, the¹⁵N assimilated into tree biomass was 29–33% of the¹⁵N added in the Douglas fir stand and less than 17% in the Scots pine stand. At the same time total¹⁵N retention in the soil (down to 70 cm) of the high-N plots was about 37% of the deposited¹⁵NH₄-N, whereas 46% and 65% of the¹⁵N was found in the soil of the low-N deposition plots at the Douglas fir and Scots pine stand, respectively. The organic layers accounted for 60% of the¹⁵N retained in the soil. The total N deposition exceeded the demand of the vegetation and microbial immobilization. Total¹⁵N leaching losses within a year (below 90 cm) were 10–20% in the high-N deposition plots in comparison to 2–6% in the lowered nitrogen input plots. Relative retention in the soil and vegetation increased at lower N-input levels.Species differences in uptake and tree health seem to contribute to lower¹⁵N recoveries in the Scots pine trees compared to the Douglas fir trees. The excessive N deposition and resulting N saturation lead to conditions were the health and functioning of biota were negatively influenced. At decreased N deposition, lower leaching losses together with increased soil and plant retention indicated a change in the fate of the¹⁵N deposited. This may have resulted from changes in ecosystem processes, and thus a shift along the continuum of N saturation to N limitation.     

Mineralization of labeled N from cowpea [Vigna unguiculata (L.) Walp.] plant parts at two growth stages in sandy soil

Cowpea [Vigna unguiculata (L). Walp.] has great potential as green manure due to its rapid N accumulation and efficient N₂ fixation. The objective of this study was to measure the rate of N mineralization from cowpea plant parts harvested at onset of flowering (5 weeks) and mid pod-fill (7 weeks) under near optimum conditions. Cowpeas were grown in a greenhouse and supplied with ¹⁵NH₄ ¹⁵NO₃ to isotopically label tissue. Cowpea leaves, stems, and roots were incorporated into a sandy soil (Psammentic Paleustalf) and net N mineralized was measured several times during a 10 week incubation. The amount of N accumulated in 7-week old cowpeas was more than double that in 5-week old cowpeas. The portion of N mineralized after 10 weeks was 24% for 5-week old cowpeas and 27% for 7-week old cowpeas. The rate of N mineralization from leaves and stems increased with plant age, but decreased for roots. The amount of N mineralized from 7-week old cowpeas was more than double (235%) that from 5-week old cowpeas due to greater N accumulation and a more rapid rate of N mineralization of the more mature cowpeas. The greatest amount of N was released from leaves, which amounted to 74 and 65% of total N mineralization from 5- and 7-week old cowpeas, respectively. The percentage of N mineralized by 10 weeks was linearly related to the tissue N concentration of the plant parts and to their C/N ratio. These relationships allow a quick estimation of the amount of N that would mineralize from cowpea residues incorporated into soil based on their N concentration or C/N ratio.