Inorganic nitrogen immobilization in live and sterile soil of old-growth conifer and hardwood forests: implications for ecosystem nitrogen retention

Rapid immobilization of inorganic nitrogen (N) in soil contributes to ecosystem N accumulation, even in old-growth and chronically-fertilized forests once thought to have poor N retention capacity. In old-growth conifer and hardwood stands in Pennsylvania, we tested the hypotheses that biotic and abiotic N immobilization are regulated by N form and forest type. We added ¹⁵NH₄ ⁺, ¹⁵NO₂ ^?, and ¹⁵NO₃ ^? to sterile (γ-irradiated) and live organic-horizon soil and define N immobilization as the mass of added ¹⁵N remaining in soil following extractions conducted 15 min, 24 h, and 21 days later. Immobilization of NO₂ ^? (19–25% of added N) occurred in sterile soils within 15 min and was little changed thereafter. Tracer NO₃ ^? immobilization was not observed, although soils had been pretreated (refrigerated) so as to quantify the lower limit of immobilization potential. Immobilization of NH₄ ⁺ (27%) occurred in live conifer soils by 21 days but not in other treatments. In 21-day incubations, tracer N immobilization was greater in NO₃ ^?-poor and humic-rich soils. Immobilization was greater in sterile than in live soil, perhaps owing to artifacts of sterilization. Conifer stands exhibited more massive O-horizons, so NO₂ ^? immobilization per unit area was greater in conifer (1.46 mg N m^?2) than hardwood (0.43 mg N m^?2) stands, possibly accounting for lower N leaching from conifer forests. Areal immobilization rates appear to be fast enough to retain all N transformed to NO₂ ^?, so NO₂ ^? production may be a limiting step in soil N retention in old-growth ecosystems.     

Estimating the organic carbon stabilisation capacity and saturation deficit of soils: a New Zealand case study

The capacity of a soil to sequester organic carbon can, in theory, be estimated as the difference between the existing soil organic C (SOC) concentration and the SOC saturation value. The C saturation concept assumes that each soil has a maximum SOC storage capacity, which is primarily determined by the characteristics of the fine mineral fraction (i.e. <20 µm clay + fine silt fraction). Previous studies have focussed on the mass of fine fractions as a predictor of soil C stabilisation capacity. Our objective was to compare single- and multi-variable statistical approaches for estimating the upper limit of C stabilisation based on measureable properties of the fine mineral fraction [e.g. fine fraction mass and surface area (SA), aluminium (Al), iron (Fe), pH] using data from New Zealand’s National Soils Database. Total SOC ranged from 0.65 to 138 mg C g^?1, median values being 44.4 mg C g^?1 at 0–15 cm depth and 20.5 mg C g^?1 at 15–30 cm depth. Results showed that SA of mineral particles was more closely correlated with the SOC content of the fine fraction than was the mass proportion of the fine fraction, indicating that it provided a much better basis for estimating SOC stabilisation capacity. The maximum C loading rate (mg C m^?2) for both Allophanic and non-Allophanic soils was best described by a log/log relationship between specific SA and the SOC content of the fine fraction. A multi-variate regression that included extractable Al and soil pH along with SA provided the “best fit” model for predicting SOC stabilisation. The potential to store additional SOC (i.e. saturation deficit) was estimated from this multivariate equation as the difference between the median and 90th percentile SOC content of each soil. There was strong evidence from the predicted saturation deficit values and their associated 95 % confidence limits that nearly all soils had a saturation deficit >0. The median saturation deficit for both Allophanic and non-Allophanic soils was 12 mg C g^?1 at 0–15 cm depth and 15 mg C g^?1 at 15–30 cm depths. Improving predictions of the saturation deficit of soils may be important to developing and deploying effective SOC sequestration strategies.     

The role of gross and net N transformation processes and NH4 + and NO3 − immobilization in controlling the mineral N pool of a temperate mixed deciduous forest soil

In many forests of Europe and north-eastern North America elevated N deposition has opened the forest N cycle, resulting in NO₃ ^? leaching. On the other hand, despite this elevated N deposition, the dominant fate of NO₃ ^? and NH₄ ⁺ in some of these forests is biotic or abiotic immobilization in the soil organic matter pool, preventing N losses. The environmental properties controlling mineral N immobilization and the variation and extent of mineral N immobilization in forest soils are not yet fully understood. In this study we investigated a temperate mixed deciduous forest, which is subjected to an average N deposition of 36.5 kg N ha^?1 yr^?1, but at the same time shows low NO₃ ^? concentrations in the groundwater. The aim of this study was to investigate whether the turnover rate of the mineral N pool could explain these low N leaching losses. A laboratory ¹⁵N pool dilution experiment was conducted to study gross and net N mineralization and nitrification and mineral N immobilization in the organic and uppermost (0–10 cm) mineral layer of the forest soil. Two locations, one at the forest edge (GE) and another one 145 m inside the forest (GF1), were selected. In the organic layers of GE and GF1, the gross N mineralization averaged 10.9 and 11.1 mg N kg^?1 d^?1, the net N mineralization averaged 6.1 and 6.8 mg N kg^?1 d^?1 and NH₄ ⁺ immobilization rates averaged 3.8 and 3.6 mg N kg^?1 d^?1. In the organic layer of GE and GF1, the average gross nitrification was 3.8 and 4.6 mg N kg^?1 d^?1, the average net nitrification was ?25.2 and ?31.3 mg N kg^?1 d^?1 and the NO₃ ^? immobilization rates averaged 29.0 and 35.9 mg N kg^?1 d^?1. For the mineral (0–10 cm) layer the same trend could be observed, but the N transformation rates were much lower for the NH₄ ⁺ pool and not significantly different from zero for the NO₃ ^? pool. Except for the turnover of the NH₄ ⁺ pool in the mineral layer, no significant differences were observed between location GE and GF1. The ratio of NH₄ ⁺ immobilization to gross N mineralization, gross N mineralization to gross nitrification, and NO₃ ^? immobilisation to gross nitrification led to the following observations. The NH₄ ⁺ pool of the forest soil was controlled by N mineralization and NO₃ ^? immobilization was importantly controlling the forest NO₃ ^? pool. Therefore it was concluded that this process is most probably responsible for the limited NO₃ ^? leaching from the forest ecosystem, despite the chronically high N deposition rates.     

Nitrogen cycling in forest soils across climate gradients in Eastern China

A ¹⁵N tracing study was carried out to investigate the potential gross nitrogen (N) dynamics in thirteen forest soils in Eastern China ranging from temperate to tropical zones (five coniferous forests, six deciduous broad-leaf forests, one temperate mixed forest, one evergreen broad-leaf forests ecosystems), and to identify the major controlling factors on N cycling in these forest ecosystems. The soil pH ranged from 4.3 to 7.9 and soil organic carbon (SOC) ranged from 6.6 g?kg^?1 to 83.0 g?kg^?1. The potential gross N transformation rates were quantified by ¹⁵N tracing studies where either the ammonium or nitrate pools were ¹⁵N labeled in parallel treatments. Gross mineralization rates ranged from 0.915 μg N g^?1 soil day^?1 to 2.718 μg N g^?1 soil day^?1 in the studied forest soils. The average contribution of labile organic-N (M _Nlab ) to total gross mineralization (M _Nrec +M _Nlab ) was 86% (58% to 99%), indicating that turnover of labile organic N plays a dominant role in the studied forest ecosystems. The gross mineralization rates in coniferous forest soils were significantly lower (ranging between 0.915 and 1.228 μg N g^?1 soil day^?1) compared to broad-leaf forest soils (ranging from 1.621 to 2.718 μg N g^?1 soil day^?1) (p?<?0.01). Thus, the dominant vegetation may play an important role in regulating soil N mineralization. Nitrate production (nitrification) occurred via two pathways, oxidation of NH ₄ ⁺ and organic N the forest soils. Correlations with soil pH indicated that this is a key factor controlling the oxidation of NH ₄ ⁺ and organic N in theses forest ecosystems. NH ₄ ⁺ oxidation decreased with a decline in pH while organic N oxidation increased. The climatic conditions (e.g. moisture status) at the various sites governed the NO ₃ ^? -N consumption processes (dissimilatory NO ₃ ^? reduction to NH ₄ ⁺ (DNRA) or immobilization of NO ₃ ^? ). Total NO ₃ ^? consumption and the proportion of total NO ₃ ^? consumption to total NO ₃ ^? production decreased with an increase in the drought index of ecosystems, showing that strong interactions appear to exist between climatic condition (e.g. the drought index), N mineralization and the rate of DNRA. Interactions between vegetation, climatic conditions govern internal N cycling in these forests soils.     

The uptake and translocation of macro- and microelements in rape and wheat seedlings as affected by selenium supply level

Plant growth in saline soils may be increased by fertilisation, but little is known about the effect of different forms of N on wheat growth in soils with different salinity levels. The aim of this study was to investigate the response of wheat (Triticum aestivum L., cv Krichauff) to (NH₄)₂SO₄ or KNO₃ or NH₄NO₃ at 0 (N0), 50 (N50), 100 (N100) and 200 (N200) mg N?kg^?1 soil in a saline sandy loam. Salinity was induced using Na⁺ and Ca²⁺ salts to achieve three EC_e levels, 2.8, 6.6 and 11.8 dS m^?1 denoted S1, S2 and S3, respectively, while maintaining a low SAR (>1). Dry weights of shoot and root were reduced by salinity in all N treatments. Addition of N significantly increased shoot and root dry weights with significant differences between N forms. Under non-saline conditions (S1), addition of NO₃???N at rates higher than N50 had a negative effect, while N100 as NH₄???N or NH₄NO₃???N increased shoot and root dry weights. At N100, shoot concentrations of N and K were higher and P, Ca, Fe, Mn, Cu and Zn were lower with NO₃???N than with NH₄???N nutrition. The concentration of all nutrients however fell in ranges did not appear to be directly associated with poor plant growth with NO₃???N. At all N additions, calculations indicated that soil salinity was highest with N addition as NO₃???N and decreased in the following order: NO₃?N > NH₄?N > NH₄NO₃?N. Addition of greater than N50 as NO₃???N, compared to NH₄???N or NH₄???NO_3, increased soil salinity and reduced micronutrient uptake both of which likely limited plant growth. It can be concluded that in saline soils addition of 100 mg N?kg^?1 as NH₄???N or NH₄NO₃???N is beneficial for wheat growth, whereas NO₃???N can cause growth depression.     

Sulfur and molybdenum fractionation in marine and riverine alluvium paddy soils

Intermittently submergence and drainage status of paddy fields can cause alterations in morphological and chemical characteristics of soils. We conducted a sequential fractionation study to provide an insight into solubility of Sulfur (S) and Molybdenum (Mo) in flooded alluvial paddy soils. The samples (0–15 and 15–30 cm) were taken from marine and riverine alluvial soils in Kedah and Kelantan areas, respectively, and were sequentially extracted with NaHCO₃, NaOH, HCl, and HClO₄–HNO₃. Total S in upper and lower layers of Kedah and Kelantan ranged between 273 and 1121 mg kg^?1, and 177 to 1509 mg kg^?1, respectively. In upper layers and subsoil of Kedah, average total Mo were 0.34 and 0.27 mg kg^?1, respectively. Average total Mo in Kelantan were 0.25 mg kg^?1 (surface layer) and 0.28 mg kg^?1 (subsoil). Cation exchange capacity (CEC) was positively correlated with plant available amounts of Mo in upper layers of Kedah area. Also, total and medium-term plant-available S was correlated with total carbon (C) at lower layers of Kelantan soil series. But in surface layers of Kelantan soil series, CEC was strongly correlated with total and medium-term plant-available S. Our results indicates that the influence of flooding conditions on soil S and Mo contents in paddy fields may cause long-term changes in S and Mo chemical reactivities.     

Wildfire Effects on Soil Gross Nitrogen Transformation Rates in Coniferous Forests of Central Idaho, USA

Forest fires often result in a series of biogeochemical processes that increase soil nitrate (NO₃ ^?) concentrations for several years; however, the dynamic nature of inorganic nitrogen (N) cycling in the plant–microbe–soil complex makes it challenging to determine the direct causes of increased soil NO₃ ^?. We measured gross inorganic N transformation rates in mineral soils 2 years after wildfires in three central Idaho coniferous forests to determine the causes of the elevated soil NO₃ ^?. We also measured key factors that could affect the soil N processes, including temperature during soil incubation in situ, soil water content, pH and carbon (C) availability. We found no significant differences (P = 0.461) in gross nitrification rates between burned and control soils. However, microbial NO₃ ^? uptake rates were significantly lower (P = 0.078) in burned than control soils. The reduced consumption of NO₃ ^? caused slightly elevated NO₃ ^? concentrations in the burned soils. C availability was positively correlated with microbial NO₃ ^? uptake rates. Despite reduced microbial NO₃ ^? uptake capacity in the burned soils, soil microbes were a strong enough N sink to maintain low soil NO₃ ^? concentrations 2 years post fire. Soil NH₄ ⁺ concentrations between the treatments were not significantly different (P = 0.673). However, gross NH₄ ⁺ production and microbial uptake rates in burned soils were significantly lower (P = 0.028 and 0.035, respectively) than in the controls, and these rates were positively correlated with C availability. Our results imply that C availability is an important factor regulating soil N cycling of coniferous forests in the region.     

Determination ofin situ KN by the chloroform fumigation-incubation method and mineralization of biomass N under anaerobic conditions

A silt loam soil from Pakistan was incubated at 30°C with increasing levels (67, 133, 200, 267 and 333 μg N g^?1 soil) of¹⁵N-labelled (NH₄)₂SO₄ and glucose (C/N ratio of 30 for all additions). At a stage when all of the applied¹⁵N was immobilized (transformed into microbial biomass), moist soil samples were subjected to the chloroform fumigation-incubation method (CFIM) for determination of K_N and microbial biomass. Mineralization of biomass derived from the applied¹⁵N and the native soil N was studied under anaerobic conditions. In situ values of K_N varied from 0.19 to 0.42 and increased with increasing levels of amendment (N + glucose). From 10 to 18% of the native soil N was found as microbial biomass. Anaerobic incubation of the soils resulted in the mineralization (determined as NH ₄ ⁺ ) of 15.08 to 29.23% of the biomass¹⁵N at different levels of amendment; 2.90 to 4.43% of the native soil N was mineralized. From 70 to 90% of the N mineralized from native soil N was derived from microbial biomass; the rest was attributed to non-biomass N.     

Temperature sensitivity of soil carbon and nitrogen mineralization: impacts of nitrogen species and land use type

Background and aims

Climate warming, nitrogen (N) deposition and land use change are some of the drivers affecting ecosystem processes such as soil carbon (C) and N dynamics, yet the interactive effects of those drivers on ecosystem processes are poorly understood. This study aimed to understand mechanisms of interactive effects of temperature, form of N deposition and land use type on soil C and N mineralization.

Methods

We studied, in a laboratory incubation experiment, the effects of temperature (15 vs. 25 °C) and species of N deposition (NH₄ ⁺-N vs. NO₃ ^?-N) on soil CO₂ efflux, dissolved organic C (DOC) and N (DON), NH₄ ⁺-N, and NO₃ ^?-N concentrations using intact soil columns collected from adjacent forest and grassland ecosystems in north-central Alberta.

Results

Temperature and land use type interacted to affect soil CO₂ efflux, concentrations of DON, NH₄ ⁺-N and NO₃ ^?-N in most measurement times, with the higher incubation temperature resulted in the higher CO₂ efflux and NH₄ ⁺-N concentrations in forest soils and higher DON and NO₃ ^?-N concentrations in grassland soils. Temperature and land use type affected the cumulative soil CO₂ efflux, and DOC, DON, NH₄ ⁺-N and NO₃ ^?-N concentrations. The form of N added or its interaction with the other two factors did not affect any of the C and N cycling parameters.

Conclusions

Temperature and land use type were dominant factors affecting soil C loss, with the soil C in grassland soils more stable and resistant to temperature changes. The lack of short-term effects of the deposition of different N species on soil C and N mineralization suggest that maybe there was a threshold for the N effect to kick in and long-term experiments should be conducted to further elucidate the species of N deposition effects on soil C and N cycling in the studied systems.     

Soil Solution Nitrogen Losses During Clearing of Lowland Amazon Forest for Pasture

Losses of nitrogen (N) often follow severe disturbance of forest ecosystems. In tropical forests, losses of N associated with the disturbance of clearing may be particularly important because rates of soil N cycling are high and forest clearing now occurs on a large scale. We measured soil solution inorganic N concentrations and fluxes for 1 year in an intact forest in the Brazilian Amazon state of Rondônia and in an adjacent 3-ha forest plot that was cleared for pasture by cutting, burning and planting pasture grass and in established cattle pastures on the same soils that were 5 and 22 years old. The cleared forest had higher soil solution NO ₃ ^? concentrations than the intact forest, but the difference between the cleared and control forests declined with time after the start of the first post-clearing rainy season. Established pastures had much lower solution NH ₄ ⁺ and NO ₃ ^? concentrations than forest or cleared forest. Estimated annual dissolved inorganic solution N fluxes to below 1 m during the first year after clearing were 2.5 kg ha^?1 in forest and 24.4 kg ha^?1 in newly cleared forest compared with only 0.5–1.2 kg ha^?1 in established pastures. The solution fluxes from cleared forest during the first year after clearing were approximately 7 times greater than gaseous N oxide (N₂O+NO) losses estimated for the same time. These results were consistent with the characterization of moist tropical forests on weathered soils as N-rich and likely to respond to disturbances that elevate soil N availability with increased loss to both soil solution and the atmosphere. These results also suggest that the relative increase in N oxide loss is substantially less than the increase solution inorganic N loss.     

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.     

Reductive soil disinfestation (RSD) alters gross N transformation rates and reduces NO and N2O emissions in degraded vegetable soils

Background and aims

Continuous vegetable cultivation in greenhouses can easily induce soil degradation, which considerably affects the development of sustainable vegetable production. Recently, the reductive soil disinfestation (RSD) is widely used as an alternative to chemical soil disinfestations to improve degraded greenhouse vegetable soils. Considering the importance of nitrogen (N) for plant growth and environment effect, the internal N transformation processes and rates should be well investigated in degraded vegetable soils treated by RSD, but few works have been undertaken.

Methods

Three RSD-treated and three untreated degraded vegetable soils were chosen and a ¹⁵?N tracing incubation experiment differentially labeled with ¹⁵NH₄NO₃ or NH₄ ¹⁵NO₃ was conducted at 25 °C under 50 % water holding capacity (WHC) for 96 h. Soil gross N transformation rates were calculated using a ¹⁵?N tracing model combined with Markov Chain Monte Carlo Metropolis algorithm (Müller et al. 2007), while the emissions of N₂O and NO were also measured.

Results

RSD could significantly enhance the soil microbial NH₄ ⁺ immobilization rate, the heterotrophic and autotrophic nitrification rates, and the NO₃ ^? turnover time. The ratio of heterotrophic nitrification to total inorganic N supply rate (mineralization + heterotrophic nitrification) increased greatly from 5.4 % in untreated vegetable soil to 56.1 % in treated vegetable soil. In addition, low release potential of NO and N₂O was observed in RSD-treated vegetable soil, due to the decrease in the NO and N₂O product ratios from heterotrophic and autotrophic nitrifications. These significant differences in gross N transformation rates, the supply processes and capacity of inorganic N, and the NO and N₂O emissions between untreated and treated vegetable soils could be explained by the elimination of accumulated NO₃ ^?, increased pH, and decreased electrical conductivity (EC) caused by RSD. Noticeably, the NO₃ ^? consumption rates were still significantly lower than the NO₃ ^? production rates in RSD-treated vegetable soil.

Conclusions

Except for improving soil chemical properties, RSD could significantly alter the supply processes of inorganic N and reduce the release potential of N₂O and NO in RSD-treated degraded vegetable soil. In order to retard the re-occurrence of NO₃ ^? accumulation, acidification and salinization and to promote the long-term productivity of greenhouse vegetable fields, the rational use of N fertilizer should be paid great attention to farmers in vegetable cultivation.     

Plant growth regulator and nitrogen fertilizer effects on soil organic carbon sequestration in creeping bentgrass fairway turf

The objective of this study was to determine the effects of plant growth regulator (PGR) (no PGR, trinexapac-ethyl, and paclobutrazol) and N fertilizer (zero N, an average of 37 kg N ha^?1 month^?1, 6 and 12 kg N ha^?1 week^?1) on soil organic C (SOC) and soil N in creeping bentgrass (Agrostis stolonifera L.) fairway turf. After 4 years of field experiments soil samples were obtained from soil depths of 0–2.5, 2.5–5, 5–7.5, 7.5–10, 10–15, 15–20, and 20–30 cm. Soil bulk density, SOC, total N, NO ₃ ^? –N, and NH ₄ ⁺ –N concentrations were determined. Paclobutrazol and trinexapac-ethyl application increased SOC. The 37 kg N ha^?1 month^?1 application increased SOC at the 0–2.5 cm depth with both PGRs. When paclobutrazol was used, N fertilizer always increased SOC; however, the greatest increase was observed with the 12 kg N ha^?1 week^?1 application when compared to other rates, inversely related to the NH ₄ ⁺ –N concentration. Nitrogen application increased soil total N and NO ₃ ^? –N in the upper three depths. The application of PGRs and N fertilizer to creeping bentgrass fairway turf is an effective strategy for promoting C sequestration.     

Nitrogen contributions from faba bean (Vicia faba L.) reliant on soil rhizobia or inoculation

Background and Aims

Understanding the impact of soil rhizobial populations and inoculant rhizobia in supplying sufficient nodulation is crucial to optimising N₂ fixation by legume crops. This study explored the impact of different rates of inoculant rhizobia and contrasting soil rhizobia on nodulation and N₂ fixation in faba bean (Vicia faba L.).

Methods

Faba beans were inoculated with one of seven rates of rhizobial inoculation, from no inoculant to 100 times the normal rate of inoculation, sown at two field sites, with or without soil rhizobia present, and their nodulation and N₂ fixation assessed.

Results

At the site without soil rhizobia, inoculation increased nodule number and increased N₂ fixation from 21 to 129 kg shoot N ha^?1, while N₂ fixation increased from 132 to 218 kg shoot N ha^?1 at the site with high background soil rhizobia. At the site without soil rhizobia, inoculation increased concentrations of shoot N from 14 to 24 mg g^?1, grain N from 32 to 45 mg g^?1, and grain yields by 1.0 Mg (metric tonne) ha^?1. Differences in nodulation influenced the contributions of fixed N to the system, which varied from the net removal of 20 kg N ha^?1 from the system in the absence of rhizobia, to a net maximum input of 199 kg N ha^?1 from legume shoot and root residues, after accounting for removal of N in grain harvest.

Conclusions

The impact of inoculation and soil rhizobia strongly influenced grain yield, grain N concentration and the potential contributions of legume cropping to soil N fertility. In soil with resident rhizobia, N₂ fixation was improved only with the highest inoculation rate.     

Seasonal and geomorphic controls on N and P removal in riparian zones of the US Midwest

Riparian zones are an important strategy to mitigate N and P export to streams. However, their efficiency with respect to nitrate (NO₃ ^?), ammonium (NH₄ ⁺), or soluble reactive phosphorus (SRP) in groundwater remains uncertain in the US Midwest. This study investigates water table fluctuations and NO₃ ^?, NH₄ ⁺, and SRP concentration dynamics in two riparian zone types (outwash vs. glacial till) common in the upper US Midwest. During low water table periods, NO₃ ^? removal was 93 % at WR (outwash site), and 75 % at LWD (glacial till site); but during high water table periods, NO₃ ^? removal efficiencies dropped to 50 % at WR, and 14 % at LWD. Median seasonal mass fluxes of NO₃ ^? removed at WR (9.4–21.7 mg N day^?1 m^?1 of stream length) and LWD (0.4–1.9 mg N day^?1 m^?1) were small compared to other riparian zones in glaciated landscapes. The WR site was a small SRP sink (0.114 and 0.118 mg day^?1 m^?1 during the dry period and wet period, respectively), while LWD acted as a small SRP source to the stream (0.004 mg day^?1 m^?1 during the dry period; 0.075 mg day^?1 m^?1 during the wet period). Both LWD and WR acted as sources of NH₄ ⁺ to the stream with mass fluxes ranging from 0.17 to 7.75 mg N day^?1 m^?1. Although riparian zones in the US Midwest provide many ecosystem services, results suggest they are unlikely to efficiently mitigate N and P pollution in subsurface flow.     

The contribution of nitrogen transformation processes to total N2O emissions from soils used for intensive vegetable cultivation

The rapid expansion of intensively farmed vegetable fields has substantially contributed to the total N₂O emissions from croplands in China. However, to date, the mechanisms underlying this phenomenon have not been completely understood. To quantify the contributions of autotrophic nitrification, heterotrophic nitrification, and denitrification to N₂O production from the intensive vegetable fields and to identify the affecting factors, a ¹⁵N tracing experiment was conducted using five soil samples collected from adjacent fields used for rice-wheat rotation system (WF), or for consecutive vegetable cultivation (VF) for 0.5 (VF1), 6 (VF2), 8 (VF3), and 10 (VF4) years. Soil was incubated under 50% water holding capacity (WHC) at 25°C for 96 h after being labeled with ¹⁵NH₄NO₃ or NH ₄ ¹⁵ NO₃. The average N₂O emission rate was 24.2 ng N?kg^?1 h^?1 in WF soil, but it ranged from 69.6 to 507 ng N?kg^?1 h^?1 in VF soils. Autotrophic nitrification, heterotrophic nitrification and denitrification accounted for 0.3–31.4%, 25.4–54.4% and 22.5–57.7% of the N₂O emissions, respectively. When vegetable soils were moderately acidified (pH, 6.2 to ?≥?5.7), the increased N₂O emissions resulted from the increase of both the gross autotrophic and heterotrophic nitrification rates and the N₂O product ratio of autotrophic nitrification. However, once severe acidification occurred (as in VF4, pH?≤?4.3) and salt stress increased, both autotrophic and heterotrophic nitrification rates were inhibited to levels similar to those of WF soil. The enhanced N₂O product ratios of heterotrophic nitrification (4.84‰), autotrophic nitrification (0.93‰) and denitrification processes were the most important factors explaining high N₂O emission in VF4 soil. Data from this study showed that various soil conditions (e.g., soil salinity and concentration of NO ₃ ^- or NH ₄ ⁺ ) could also significantly affect the sources and rates of N₂O emission.     

Biogeochemistry of terrestrial soils as influenced by short-term flooding

Many terrestrial soils in the US Midwest are temporally flooded during the spring. The effects of short-term flooding on biogeochemical processes that occur in these soils are not fully understood and are the subject of this study. To evaluate these processes we investigated the redox-induced changes in the soil solution for three-cultivated and three-uncultivated/forest soils with different organic matter concentrations. The soils were flooded for 1, 3, 7, and 14-days under anoxic conditions in a biogeochemical reactor. Samples were analyzed for Eh; pH; NO₃ ^?; NH₄ ⁺; total dissolved Mn and Fe; soluble P; dissolved organic and inorganic carbon (DOC–DIC); and evolved CO₂. We found strongly contrasting responses of the terrestrial soils to flooding. Reducing conditions were established quickly in the uncultivated and more slowly in the cultivated soils. Concomitant changes in pH were higher for the uncultivated soils. The uncultivated soils showed a higher increase in the amount of NH₄ ⁺, P, Fe, Mn than the cultivated soils over the 14-day incubation. The total amount of carbon decomposed was much greater for the uncultivated soils with approximately 900 μg C (CO₂ + DOC + DIC) decomposed per gram of soil compared to a total decomposition of 240 μg C g _soil ^?1 for the cultivated soils indicating differences in the type of carbon decomposed. The rapid onset of reducing conditions for the uncultivated soils is attributed to a reactive carbon component that is either absent or occluded in the cultivated soils. This study demonstrates that the biogeochemically-induced changes in carbon dynamics in terrestrial soils are strongly influenced by short-term flooding and the history of soil management.     

Potential nitrogen and carbon processing in a landscape rich in milldam legacy sediments

Recent identification of the widespread distribution of legacy sediments deposited in historic mill ponds has increased concern regarding their role in controlling land–water nutrient transfers in the mid-Atlantic region of the US. At Big Spring Run in Lancaster, Pennsylvania, legacy sediments now overlay a buried relict hydric soil (a former wetland soil). We compared C and N processing in legacy sediment to upland soils to identify soil zones that may be sources or sinks for N transported toward streams. We hypothesized that legacy sediments would have high nitrification rates (due to recent agricultural N inputs), while relict hydric soils buried beneath the legacy sediments would be N sinks revealed via negative net nitrification and/or positive denitrification (because the buried former wetland soils are C rich but low in O₂). Potential net nitrification ranged from 9.2 to 77.9 g m^?2 year^?1 and potential C mineralization ranged from 223 to 1,737 g m^?2 year^?1, with the highest rates in surface soils for both legacy sediments and uplands. Potential denitrification ranged from 0.37 to 21.72 g m^?2 year^?1, with the buried relict hydric soils denitrifying an average of 6.2 g m^?2 year^?1. Contrary to our hypothesis, relict hydric layers did not have negative potential nitrification or high positive potential denitrification rates, in part because microbial activity was low relative to surface soils, as indicated by low nitrifier population activity, low substrate induced respiration, and low exoenzyme activity. Despite high soil C concentrations, buried relict hydric soils do not provide the ecological services expected from a wetland soil. Thus, legacy sediments may dampen N removal pathways in buried relict hydric soils, while also acting as substantial sources of NO₃ ^? to waterways.     

Stable N isotope composition of nitrate reflects N transformations during the passage of water through a montane rain forest in Ecuador

Knowledge of the fate of deposited N in the possibly N-limited, highly biodiverse north Andean forests is important because of the possible effects of N inputs on plant performance and species composition. We analyzed concentrations and fluxes of NO₃ ^??CN, NH₄ ⁺?CN and dissolved organic N (DON) in rainfall, throughfall, litter leachate, mineral soil solutions (0.15?C0.30 m depths) and stream water in a montane forest in Ecuador during four consecutive quarters and used the natural ¹⁵N abundance in NO₃ ^? during the passage of rain water through the ecosystem and bulk ??¹⁵N values in soil to detect N transformations. Depletion of ¹⁵N in NO₃ ^? and increased NO₃ ^??CN fluxes during the passage through the canopy and the organic layer indicated nitrification in these compartments. During leaching from the organic layer to mineral soil and stream, NO₃ ^? concentrations progressively decreased and were enriched in ¹⁵N but did not reach the ??¹⁵N values of solid phase organic matter (??¹⁵N = 5.6?C6.7??). This suggested a combination of nitrification and denitrification in mineral soil. In the wettest quarter, the ??¹⁵N value of NO₃ ^? in litter leachate was smaller (??¹⁵N = ?1.58??) than in the other quarters (??¹⁵N = ?9.38 ± SE 0.46??) probably because of reduced mineralization and associated fractionation against ¹⁵N. Nitrogen isotope fractionation of NO₃ ^? between litter leachate and stream water was smaller in the wettest period than in the other periods probably because of a higher rate of denitrification and continuous dilution by isotopically lighter NO₃ ^??CN from throughfall and nitrification in the organic layer during the wettest period. The stable N isotope composition of NO₃ ^? gave valuable indications of N transformations during the passage of water through the forest ecosystem from rainfall to the stream.     

High tolerance of aluminum in the grass species Cynodon aethiopicus

Concentrations of aluminum (Al) were determined in leaves of native terrestrial plants, macrophytes and fruit parts (watermelon and tomato) using inductively coupled plasma mass spectrometry. Al concentrations in water and soil were determined by inductively coupled plasma optical emission spectrometry. Potamogeton thunbergii (macrophyte) and Cynodon aethiopicus (terrestrial grass) had the highest leaf Al concentrations (2 and 1 g kg^?1 dw, respectively). Transfer factors (mg kg^?1 dw plants/mg kg^?1 dw soil) based on total Al concentrations in soil varied from 2 × 10^?3 to 0.05 and from 1.9 to 78 based on mobile Al concentrations determined after sequential extraction. Bioconcentration factors (mg kg^?1 dw plants/mg L^?1 water) varied from 19 to 9.5 × 10³ L kg^?1 dw. Plants can accumulate high concentrations of Al when growing in neutral pH soils and slightly alkaline lakes in the Ethiopian Rift Valley. Controlled experiments showed that C. aethiopicus can accumulate high levels of Al both in root and shoot. Compared to Arabidopsis thaliana, C. aethiopicus was more tolerant to Al exposure as ≥400 μM AlCl₃ was needed to inhibit root growth compared to 200 μM in A. thaliana. After exposing C. aethiopicus and A. thaliana in 800 μM AlCl_3, alkaline comet assay indicates significant DNA (deoxyribonucleic acid) damage in A. thaliana while C. aethiopicus was unaffected. No significant induction of reactive oxygen species (ROS), in terms of leaf H₂O₂ levels, could be observed in C. aethiopicus. C. aethiopicus has mechanisms to suppress both Al-induced ROS and DNA damage, thereby increasing tolerance of the species to high Al concentrations.