Contribution of dissolved organic nitrogen deposition to total dissolved nitrogen deposition under intensive agricultural activities

For elucidating the atmospheric deposition contribution of dissolved organic nitrogen (DON) to the total dissolved nitrogen (TDN) deposition rate, dissolved inorganic nitrogen (DIN: NH₄ ⁺ + NO₃ ^–) and DON deposition rates were annually and monthly estimated during 4 and half-yr monitoring period in an experimental multi-farm under intensive agricultural activities of N fertilizer use and animal husbandry in Central Japan. Annual NH₄ ⁺, DON and NO₃ ^– deposition rates in bulk and wet deposition data accounted for 48%, 32% and 20% of TDN deposition, respectively, which indicated that this area is strongly affected by the intensive agricultural activities. The DIN and DON deposition rates were respectively estimated at 21.6 and 10.1 kg N ha^?1 yr^?1, which ranked high in a worldwide regional data set. Consequently, this area has been exposed to a large amount of N deposition including DON with N fertilizer input. The difference between bulk and wet deposition rates (NH₄ ⁺ and DON) is one of important factors controlling the N deposition in this area. Monthly DON deposition showed positive correlations with DIN and NH₄ ⁺ deposition rates, respectively, with a significant linear regression curve. The linear regression curve of our monthly data (n = 127) indicates the same trend as the worldwide annual data set (n = 31).     

Sediment denitrification in waterways in a rice-paddy-dominated watershed in eastern China

Purpose

Rice-paddy-dominated watersheds in eastern China are intensively cultivated, and lands with two crops receive as much as 550–600 kg?ha^–1?year^–1 of nitrogen (N), mainly through the addition of N-based fertilizers. However, stream N concentrations have been found to be relatively low. Waterways in the watersheds are assumed to be effective “sinks” for N, minimizing its downstream movement. We directly measured net sediment denitrification rates in three types of waterways (ponds, streams/rivers, and a reservoir) and determined the key factors that control net sediment denitrification. Such information is essential for evaluating the impact of the agricultural N cycle on the quality of surface water.

Materials and methods

The pond–stream–reservoir continuum was sampled every 2 months at nine sites in an agricultural watershed between November 2010 and December 2011. Net sediment N₂ fluxes/net sediment denitrification rates were determined by membrane inlet mass spectrometry and the N₂/Ar technique. A suite of parameters known to influence denitrification were also measured.

Results and discussion

Net denitrification rates ranged between 28.2?±?18.2 and 674.3?±?314.5 μmol N₂–N?m^–2?h^–1 for the streams, 23.7?±?23.9 and 121.2?±?38.7 μmol N₂–N?m^–2?h^–1 for the ponds, and 41.8?±?17.7 and 239.3?±?49.8 μmol N₂–N?m^–2?h^–1 for the reservoir. The mean net denitrification rate of the stream sites (173.2?±?248.4 μmol N₂–N?m^–2?h^–1) was significantly higher (p?<?0.001) than that of the pond sites (48.3?±?44.5 μmol N₂–N?m^–2?h^–1), and the three types of waterways all had significantly higher (p?<?0.01) mean net denitrification rates in summer than in other seasons. Linear regression and linear mixed effect model analysis showed that nitrate (NO₃ ^?–N) concentration in surface water was the primary controlling factor for net sediment denitrification, followed by water temperature. Using monitoring data on NO₃ ^?–N concentrations and temperature of the surface water of waterways and an established linear mixed effect model, total N removed through net sediment denitrification in the pond–stream–reservoir continuum was estimated at 46.8?±?24.0 t?year^–1 from July 2007 to June 2009, which was comparable with earlier estimates based on the mass balance method (34.3?±?12.7 t?year^–1), and accounted for 83.4 % of the total aquatic N. However, the total aquatic N was only 4.4 % of the total N input to the watershed, and thus most of the surplus N in the watershed was likely to be either denitrified or stored in soil.

Conclusions

High doses of N in a rice-paddy-dominated watershed did not lead to high stream N concentrations due to limited input of N into waterways and the high efficiency of waterways in removing N through denitrification.     

Nitrogen Leaching of Two Forest Ecosystems in a Karst Watershed

Karst watersheds are a major source of drinking water in the European Alps. These watersheds exhibit quick response times and low residence times, which might make karst aquifers more vulnerable to elevated nitrogen (N) deposition than non-karst watersheds. We summarize 13 years of monitoring NO ₃ ^? , NH ₄ ⁺ , and total N in two forest ecosystems, a Norway spruce (Picea abies (L.) Karst.) forest on Cambisols/Stagnosols (IP I) and a mixed beech (Fagus sylvatica L.) spruce forest on Leptosols (IP II). N fluxes are calculated by multiplying concentrations, measured in biweekly intervals, with hydrological fluxes predicted from a hydrological model. The total N deposition in the throughfall amounts to 26.8 and 21.1 kg/ha/year in IP I and IP II, respectively, which is high compared to depositions found in other European forest ecosystems. While the shallow Leptosols at IP II accumulated on average 9.2 kg/ha/year of N between 1999 and 2006, the N budgets of the Cambisols/Stagnosols at IP I were equaled over the study period but show high inter-annual variation. Between 1999 and 2006, on average, 9 kg/ha/year of DON and 20 kg/ha/year of DIN were output with seepage water of IP I but only 4.5 kg/ha/year of DON and 7.7 kg/ha/year of DIN at IP II. Despite high DIN leaching, neither IP I nor IP II showed further signs of N saturation in their organic layer C/N ratios, N mineralization, or leaf N content. The N budget over all years was dominated by a few extreme output events. Nitrate leaching rates at both forest ecosystems correlated the most with years of above average snow accumulation (but only for IP I this correlation is statistically significant). Both snow melt and total annual precipitation were most important drivers of DON leaching. IP I and IP II showed comparable temporal patterns of both concentrations and flux rates but exhibited differences in magnitudes: DON, NO ₃ ^? , and NH ₄ ⁺ inputs peak in spring, NH ₄ ⁺ showed an additional peak in autumn; the bulk of the annual NO ₃ ^? and DON output occurred in spring; DON, NO ₃ ^? , and NH ₄ ⁺ output rates during winter months were low. The high DIN leaching at IP I was related to snow cover effects on N mineralization and soil hydrology. From the year 2004 onwards, disproportional NO ₃ ^? leaching occurred at both plots. This was possibly caused by the exceptionally dry year 2003 and a small-scale bark beetle infestation (at IP I), in addition to snow cover effects. This study shows that both forest ecosystems at Zöbelboden are still N limited. N leaching pulses, particularly during spring, dictate not only annual but also the long-term N budgets. The overall magnitude of N leaching to the karst aquifer differs substantially between forest and soil types, which are found in close proximity in the karstified areas of the Northern Limestone Alps in Austria.     

Ammonium Nitrogen Deposition as a Dominant Source of Nitrogen in a Forested Watershed Experiencing Acid Rain in Central Japan

To clarify nitrogen (N) sources, the overall N budget in a forested watershed in Kanagawa Prefecture, Central Japan was estimated by measuring dissolved inorganic N (DIN; NH₄ ⁺ + NO₃ ^– + NO₂ ^–) from Nov 2004 through Oct 2005. The estimated N budget (–1.43 kg N ha^–1 year^–1) showed that the N output rate (stream water N) was higher than the N input rate (bulk deposition N) in the watershed. The annual NO₂ ^– and NO₃ ^– input rates were 0.02 and 1.99 kg N ha^–1 year^–1, respectively. NH₄ ⁺ was the predominant source in this forested watershed, accounting for 71% (4.99 kg N ha^–1 year^–1) of DIN input rate. In addition, this study estimated rainfall pH, air temperature, and wind direction, which were considered as controlling factors related to the atmospheric deposition rate of NH₄ ⁺. This study showed that the rainfall NH₄ ⁺ was inversely proportional to the initial pH of the rainfall, which was calculated by adding the amount of H⁺ consumed by the dissociation process of NH_3(aq) to the measured rainfall pH. This result implies that acid rain can elevate the solubility of NH_3(g) and the dissociation capacity of NH₄ ⁺ throughout the process of precipitation. Also, this study provides strong evidence that the high NH₄ ⁺ deposition rate is mainly derived from NH_3(g) emitted from livestock wastes under the NH₃ transport condition of warm summer and favorable wind direction.     

Effects of Land Use Conversion from Native Forests to Exotic Plantations on Nitrogen and Phosphorus Retention in Catchments of Southern Chile

In six small catchments located at the Cordillera de la Costa in southern Chile (40° S), concentrations and fluxes of NO₃-N, NH₄-N, organic-N, total-N and total-P in bulk precipitation and runoff water were measured. The main objective of this study was to compare nitrogen and phosphorus retention of catchments with varying land cover of native forest and exotic plantations, in order to evaluate possible effects of land use change. Nitrate-N was the dominant fraction (>50%) of nitrogen loss, especially in the catchments dominated by exotic plantations. In the catchment with native forests, NO₃ ^? only contributed with 34% of the nitrogen loss and DON was the main output with 55%. Annual NO₃ ^? export was lower in the catchment with native forest compared to the catchments with exotic plantations where the streamflow output exceed the precipitation input. Average inputs of total-N were 2.6 kg ha^?1 year^?1 (DIN?=?1.4 kg ha^?1 year^?1, DON?=?1.2 kg ha^?1 year^?1) and outputs were 1.7 kg ha^?1 year^?1 (DIN?=?1.2 kg ha^?1 year^?1, DON?=?0.5 kg ha^?1 year^?1). Annual retention of total nitrogen fluctuated between 61% in a catchment dominated by native forests to 15% in catchments dominated by exotic plantations of Eucalyptus sp. Nitrogen retention was positively related with native forest coverage. The N retention capacity of the catchments could be both attributed to consequences of clear cutting practices and differences in vegetation cover.     

Microbial decomposition of leached or extracted dissolved organic carbon and nitrogen from pasture soils

Microbial decomposition of extracted and leached dissolved organic carbon (DOC) and nitrogen (DON) was demonstrated from three pasture soils in laboratory incubation studies. DOC concentration in water extracts ranged between 29 and 148 mg C L^?1 and DON concentration ranged between 2 and 63 mg N L^?1. Between 17 and 61 % of the DOC in the water extracts were respired as CO₂ by microbes by day 36. DON concentrations in the extracts declined more rapidly than DOC. Within the first 21 days of incubation, the concentration of DON was near zero without any significant change in the concentration of NO₃ ^? or NH₄ ⁺, indicating that microbes had utilized the organic pool of N preferentially. Decomposition of leached DOC (ranged between 7 and 66 mg C L^?1) and DON (ranged between 6 and 11 mg N L^?1) collected from large lysimeters (with perennial pasture; 50 cm diameter?×?80 cm deep) followed a similar pattern to that observed with soil extracts. Approximately 28 to 61 % of the DOC in leachates were respired as CO₂ by day 49. The concentration of DON in the leachates declined to below 1 mg N L^?1 within 7–14 days of the incubation, consistent with the observations made with extractable DON. Our results clearly show that DOC and DON components of the dissolved organic matter in pasture soils, whether extracted or leached, are highly decomposable and bioavailable and will influence local ecosystem functions and nutrient balances in grazed pasture systems and receiving water bodies.     

Soil C/N Ratio as Affected by Climate: An Ecological Factor of Forest NO3 − Leaching

The soil nitrogen cycle was investigated for several watershed forests of which stream waters have distinctively different nitrate (NO₃ ^?) concentrations. In a watershed with stream water NO₃ ^? of more than 100 µM, soil NO₃ ^? content increased even beneath the rooting zone, revealing "nitrogen saturation" status. A laboratory soil experiment demonstrated that the proportion of net NO₃ ^? production to CO₂ production was largely regulated by a soil C/N ratio, suggesting a key parameter for NO₃ ^? abundance. In the respective watershed soils, little nitrogen was actually present as NO₃ ^? above a soil C/N ratio of 20. The annual mean soil temperature recorded at the sites was correlated with a shift in the C/N ratio in watershed soils (a soil C/N ratio increase of 0.5 per 1°C decrease) along the stream NO₃ ^? gradient of 30 fold. The results suggest that soil microbial metabolisms affected by C/N ratio may be a direct agent regulating NO₃ ^? leaching from watersheds under the influence of an atmospheric nitrogen load and climate.     

Determining nitrogen fate by hydrological pathways and impact on carbonate weathering in an agricultural karst watershed

Identifying the nitrogen (N) fate is complicated and a great challenge in karst watersheds because of the co-existence of natural pools and anthropogenic sources. The objective of the study was to use stable isotopic composition of dual-isotope (δ¹⁵N_Nitrate and δ¹⁸O_Nitrate) and LOADEST model approaches to trace N sources, pathways in karst watershed. The study was conducted in the Houzhai watershed, which is a typical agricultural karst watershed from July 2016 to August 2018, to reveal the N fate and the coupled carbon(C)–N processes occurring in the riverine-watershed with agricultural activities. We found that the wet deposition of total nitrogen (TN) flux was 33.50 kg hm⁻²·a⁻¹ and dissolved nitrogen (DN) flux was 21.66 kg hm⁻²·a⁻¹. The DN runoff loss was 2.10 × 10⁵ kg·a⁻¹ and the loss of DN during the wet season accounted for 95.4% over a year. In the wet season, NO₃⁻-N daily efflux was 977.62 ± 516.66 kg ha⁻¹·day⁻¹and 248.77 ± 57.83 kg ha⁻¹·day⁻¹ in the dry season. The NH₄⁺-N efflux was 29.17 ± 10.50 kg ha⁻¹·day⁻¹ and 4.42 ± 3.07 kg ha⁻¹·day⁻¹ in the wet and dry seasons, respectively. The main form output load of N was NO₃⁻-N which was more than 30 times as much as NH₄⁺-N output loss. The NO₃⁻-N caused by rainfall contributed 11.82%–53.61% to the export load. Nitrate from soil contributed over 94% of the N to Houzhai river caused by N leaching. In addition, manure and farmland soil were the main sources of groundwater in the Houzhai watersheds, the contribution rates were 25.9% and 22.5%. The chemical N fertilizers affected carbonate weathering strongly, and the HCO₃⁻ flux caused by nitrification due to N fertilizers application in soil accounted for 23.5% of the entire watershed. This study suggested that carbonate weathering may be influenced by nitrogen nitrification in the karst watershed.     

Dissolved organic carbon and nitrogen dynamics in temperate coniferous forest plantations

Dissolved organic matter (DOM) plays a central role in driving many chemical and biological processes in soil; however, our understanding of the fluxes and composition of the DOM pool still remains unclear. In this study we investigated the composition and dynamics of dissolved organic carbon (DOC) and nitrogen (DON) in five temperate coniferous forests. We subsequently related our findings to the inputs (litterfall, throughfall, atmospheric deposition) and outputs (leaching, respiration) of C and N from the forest and to plant available sources of N. With the exception of NO₃^?, most of the measured soil solution components (e.g. DOC, DON, NH₄⁺, free amino acids, total phenolics and proteins) progressively declined in concentration with soil depth, particularly in the organic horizons. This decline correlated well with total microbial activity within the soil profile. We calculated that the amount of C lost by soil respiration each day was equivalent to 70% of the DOC pool and 0.06% of the total soil C. The rapid rate of amino acid mineralization and the domination of the low molecular weight soluble N pool by inorganic N suggest that the microbial community is C‐ rather than N‐limited and that C‐limitation increases with soil depth. Further, our results suggest that the forest stands were not N‐limited and were probably more reliant on inorganic N as a primary N source rather than DON. In conclusion, our results show that the size of the DON and DOC pools are small relative to both the amount of C and N passing through the soil each year and the total C and N present in the soil. In addition, high rates of atmospheric N deposition in these forests may have removed competition for N resources between the plant and microbial communities.     

Leaching of nitrogen from a forest catchment at söder»sen in southern Sweden

Water balance and leaching of plant nutrients, with special reference to N, were described for a 46-ha catchment consisting mainly of coniferous forest (one third of it clear-cut) during the period January 1982-August 1988. The atmospheric N load in this region is high compared with most other parts of Scandinavia. On average, annual N leaching amounted to 9.5 kg ha^?1 in the form of NO₃-N (83%), org-N (15%) and NH₄-N (2%). The highest monthly rate of N transport observed was 3.9 kg ha^?1. The NO₃-N levels in groundwater in the 60-yr-old coniferous stand ranged from 0.5 to 3.1 mg L^?1. The effect of clear-cutting on groundwater-NO₃-N levels lasted 4 yr. The highest annual NO₃-N transport from the clear-cut area observed was 18 kg ha^?1. The groundwater in the spruce forest was very acidic (pH=4.3) in contrast to the stream water (pH=6.3). The relatively higher pH-value of the stream water was probably a result of chemical and biological processes occurring in the highly humified, periodically waterlogged peat soil (alder swamp) in the vicinity of the small stream.     

Influence of temperature and vegetation cover on soluble inorganic and organic nitrogen in a spodosol

In this study, the influence of temperature and vegetation cover on soluble inorganic and organic nitrogen in a spodosol from north east Scotland was investigated. Firstly, soil cores were incubated at 5, 10 and 15°C for up to 8 weeks. Net mineralisation was observed at all temperatures with larger rates observed at higher temperatures. In contrast, water extractable dissolved organic nitrogen (DON) displayed no clear trend with time and showed little response to temperature. Secondly, intact cores of the same soil, with and without vegetation, were leached with artificial rain for 6 weeks at 6.5 and 15°C. Temperature and the presence of vegetation interacted to have a significant (P<0.01) effect on the concentration of NO₃⁻ in leachates; highest concentrations were observed in leachates from cores without vegetation at 15°C, whereas lowest concentrations were observed in leachates from cores with vegetation at 6.5°C. In contrast, concentrations of DON and dissolved organic carbon (DOC) were significantly (P<0.001) higher in leachates from cores with vegetation than without vegetation and were not affected by temperature. The cumulative amounts of DON and DOC leached from the cores with vegetation were 4 and 2.5 times greater, respectively, than those leached from the cores without vegetation. Comparison of soil solution (extracted by centrifugation at 0–5 and 5–10 cm depth) after leaching for 6 weeks, showed that the upper layer contained more than twice the amount of DON than the 5–10 cm layer and that the difference in concentration between the two depths was enhanced in the presence of vegetation. The results indicate that vegetation is an important source of DON and DOC. However, the removal of vegetation did not lead to an increase in the quantity of total dissolved nitrogen (TDN) in soil water, but resulted in a change in the dominant N fraction from DON to NO₃⁻. In addition, the results show that DON, in both the incubated and leached cores, did not change as inorganic N was mineralised. This suggests that if water extractable DON was acting as a source of NH₄⁺ or NO₃⁻, then it was being replenished by, and in equilibrium with, a large reserve of organic N. Evidence of such a pool was indirect in the form of additional DON (equivalent to 2 g N m⁻²) being extracted by 0.5 M K₂SO₄.     

Amino acid,peptide and protein mineralization dynamics in a taiga forest soil

The availability of inorganic N has been shown to be one of the major factors limiting primary productivity in high latitude ecosystems. The factors regulating the rate of transformation of organic N to nitrate and ammonium, however, remain poorly understood. The aim of this study was to investigate the nature of the soluble N pool in forest soils and to determine the relative rate of inorganic N production from high and low molecular weight (MW) dissolved organic nitrogen (DON) compounds in black spruce forest soils. DON was found to be the dominant N form in soil solution, however, most of this DON was of high MW of which >75% remained unidentified. Free amino acids constituted less than 5% of the total DON pool. The concentration of NO₃⁻ and NH₄⁺ was low in all soils but significantly greater than the concentration of free amino acids. Incubations of low MW DON with soil indicated a rapid processing of amino acids, di- and tri-peptides to NH₄⁺ followed by a slower transformation of the NH₄⁺ pool to NO₃⁻. The rate of protein transformation to NH₄⁺ was slower than for amino acids and peptides suggesting that the block in N mineralization in taiga forest soils is the transformation of high MW DON to low MW DON and not low MW DON to NH₄⁺ or NH₄⁺ to NO₃⁻. Calculated turnover rates of amino acid-derived C and N immobilized in the soil microbial biomass were similar with a half-life of approximately 30 d indicating congruent C and N mineralization.     

Amounts and relative significance of runoff types in the transport of nitrogen into a stream draining an agricultural watershed

The concentration and amounts of NO₃-N and TN transported in surface, accelerated subsurface, and subsurface runoff and stream flow draining a 20 ha pasture watershed were measured over a period of 3 yr. A slight decrease and increase of NO₃-N and particulate N concentrations, respectively, were obtained with increased flow of the runoff types and stream, due to dilution and increased sediment transport, respectively. The concentration of NO₃-N in surface, accelerated subsurface and subsurface runoff and stream flow averaged for the 3 yr was 0.3, 6.6, 4.8, and 4.6 mg 1^?1, respectively, amounting to 0.5, 9.4, 11.6, and 16.8 kg ha^?1 yr^?1, respectively, transported annually. Although NO₃-N accounted for only a minor proportion of the TN transported in surface runoff (10%) it was the main form of N (75%) transported in the other runoff types and in streamflow. Subsurface runoff contributed the major proportion of stream discharge (63%), and NO₃-N (69%), particulate N (44%) and TN (65%) loading of the stream. The results are discussed in terms of non-point pollution of surface waters by NO₃-N.     

Estimating potentials for nitrate-N reduction and nitrogen transformations from field incubations

Fine-textured soil cores were saturated with KNO₃ solutions, withdrawn at periodic in tervals and examined for mineral N forms. Reduction of NO₃^? was correlated with time using a first-order rate function. Instantaneous initial NO₃^?-N reduction rates were determined by taking derivatives of the rate function and setting t = 0. Duplicate experiments gave maximum NO₃^?-N reduction rates of 1.0 μ N/g soil/h or ? 100 kg NO₃^?-N/ha/day. Calculated NO₃^? reduction rates increased with depth down to 30 cm. Net NO₃^?-N reduction ceased between 48 and 96 h after which net NO₃^?-N production of 0.016 to 0.29 μg N/g soil/h (～1.5 kg N/ha/day/0 to 20 cm) occurred. Net NH₄⁺-N mineralization ranged from about 0.03 to 0.05 μg N/g soil/h (3.5 to 4.0 kg N/ha/day/0 to 30 cm). Both instantaneous initial NO₃^?-N loss rates and N mineralization rates are similar to results of laboratory studies elsewhere on similar soil types. This procedure for estimating N-transformations may be useful where other techniques are either not adequate or not feasible for field use.     

Severe soil frost reduces losses of carbon and nitrogen from the forest floor during simulated snowmelt: A laboratory experiment

Considerable progress has been made in understanding the impacts of soil frost on carbon (C) and nitrogen (N) cycling, but the effects of soil frost on C and N fluxes during snowmelt remain poorly understood. We conducted a laboratory experiment to determine the effects of soil frost on C and N fluxes from forest floor soils during snowmelt. Soil cores were collected from a sugar maple (Acer saccharum)–American beech (Fagus grandifolia) and a red spruce (Picea rubens)–balsam fir (Abies balsamea) forest at the Hubbard Brook Experimental Forest in New Hampshire, U.S.A. Soils were exposed to one of three temperature treatments, including severe (?15 °C), mild (?0.5 °C), and no soil frost (+5 °C) conditions. After one week the soils were incubated at +5 °C and snow was placed on top of the soils to simulate spring snowmelt. NO₃^? losses were up to 5.5 mg N kg^?1 soil greater in the mild soil frost treatment than the severe soil frost treatment. Net losses of NH₄⁺ and DON in leachate were up to 19 and 18 mg N kg^?1 soil greater in the no soil frost and mild soil frost treatments, respectively, than the severe soil frost treatment. In contrast, soil frost did not have a significant impact on dissolved organic C or cumulative gaseous fluxes of C and N throughout the snowmelt period. However, the total cumulative flux of C (i.e. dissolved organic C + CO₂ + CH₄) and N (i.e. dissolved organic N + NH₄ + NO₃ + N₂O) in the severe soil frost treatment were between one quarter and one half that observed in the no soil frost treatment for both forest types. Together, the results of this study show that total fluxes of N in leachate, as well as total cumulative C and N fluxes (gases + leachate), were significantly reduced following severe soil frost. We conclude that the extent to which C and N cycling during snowmelt is altered in response to changes in winter climate depend on both the presence and severity of soil frost.     

Photochemical Formation of OH Radicals in Dew Formed on the Pine Needles at Mt. Gokurakuji

Photochemical formation rates and sources of the hydroxyl (OH) radical were determined in dew water formed on the surface of Japanese red pine (Pinus densiflora) needles of declining (NO₂ polluted area) and healthy pine stands at Mt. Gokurakuji located west of Hiroshima city in western Japan. The measured OH radical photoformation rates in dew water (n=10), which were normalized to the rate at midday on May 1 at 34°N, ranged from 0.67 to 5.18 µM h^?1 (1M=1mol L^?1). The mean value (2.69 µM h^?1) was higher than that in dew water collected on a Teflon board and higher than the mean value in rain water published previously. Of the total OH radical formation rate observed in dew water on the pine needles, 16.4 % was estimated to originate from N (III) (NO₂ ^? and HNO₂) and 24.6 % was estimated to originate from NO₃ ^?. There were other sources of OH radical photochemical formation in dew water on the pine needles besides photolysis of NO₂ ^? and NO₃ ^?.     

pH change, carbon and nitrogen mineralization in paddy soils as affected by Chinese milk vetch addition and soil water regime

Purpose

The aim of the research was to explore the effect of Chinese milk vetch (CM vetch) addition and different water management practices on soil pH change, C and N mineralization in acid paddy soils.

Materials and methods

Psammaquent and Plinthudult paddy soils amended with Chinese milk vetch at a rate of 12 g?kg^?1 soil were incubated at 25 °C under three different water treatments (45 % field capacity, CW; alternating 1-week wetting and 2-week drying cycles, drying rewetting (DRW) and waterlogging (WL). Soil pH, dissolved organic carbon, dissolved organic nitrogen (DON), CO₂ escaped, microbial biomass carbon, ammonium (NH₄ ⁺) and nitrate (NO₃ ^?) during the incubation period were dynamically determined.

Results and discussion

The addition of CM vetch increased soil microbial biomass concentrations in all treatments. The CM vetch addition also enhanced dissolved organic N concentrations in all treatments. The NO₃–N concentrations were lower than NH₄–N concentrations in DRW and WL. The pH increase after CM vetch addition was 0.2 units greater during WL than DRW, and greater in the low pH Plinthudult (4.59) than higher pH Paleudalfs (6.11) soil. Nitrogen mineralization was higher in the DRW than WL treatment, and frequent DRW cycles favored N mineralization in the Plinthudult soil.

Conclusions

The addition of CM vetch increased soil pH, both under waterlogging and alternating wet–dry conditions. Waterlogging decreased C mineralization in both soils amended with CM vetch. Nitrogen mineralization increased in the soils subjected to DRW, which was associated with the higher DON concentrations in DRW than in WL in the acid soil. Frequent drying–wetting cycles increase N mineralization in acid paddy soils.     

Carbon and nitrogen turnover in response to warming and nitrogen addition during early stages of forest litter decomposition—an incubation experiment

Purpose

Little is known about the interactive effects of temperature, nitrogen (N) supply, litter quality, and decomposition time on the turnover of carbon (C) and N of forest litter. The objective of this study was to investigate the interactive effects of warming, N addition and tree species on the turnover of C and N during the early decomposition stage of litters in a temperate forest.

Materials and methods

A 12-week laboratory incubation experiment was carried out. The leaf litters including two types of broadleaf litters (Quercus mongolica and Tilia amurensis), a needle litter (Pinus koraiensis), and a mixed litter of them were collected from a broad-leaved Korean pine mixed forest ecosystem in northeastern China in September 2009. Nine treatments were conducted using three temperatures (15, 25, and 35 °C) combined with three doses of N addition (equal to 0, 75, and 150 kg?·?ha^?1?a^?1, respectively, as NH₄NO₃).

Results and discussion

After 12 weeks of incubation, the mass loss ranged between 12 and 35 %. The broadleaf litters had greater mass loss and cumulative CO₂–C emission than the needle litter. Temperature and N availability interacted to affect litter mass loss and decomposition rate. The dissolved organic carbon (DOC) and nitrogen (DON) concentrations in litter leachate varied widely with litter types. DOC increased significantly with increased temperature but decreased significantly with increased N availability. DON increased significantly with increased N availability but showed a higher level at the moderate decomposition temperature. The amounts of CO₂ and N₂O emission were significantly higher at 25 °C than those at 15 and 35 °C, and were significantly increased by the N addition.

Conclusions

The present study indicated relatively intricate temperature and N addition effects on C and N cycling during early stages of litter decomposition, implying that future increases in temperature and N deposition will directly affect C and N cycling in broad-leaved Korean pine mixed forest ecosystem, and may indirectly influence the ecosystem composition, productivity, and functioning in NE China. It is, therefore, important to understand the interactive effects of biotic and abiotic factors on litter decomposition in field conditions in order to assess and predict future ecosystem responses to environmental changes in NE China.     

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

Purpose

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

Materials and methods

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

Results and discussion

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

Conclusions

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

     

Regional Distribution of Natural Stream Nitrate in Central Japan

Over 60 natural streams with forested catchments were surveyed for nitrate (NO₃ ^?) concentration in central Japan. Stream NO₃ ^? concentrations showed a clear zonal gradient with a range nearly as large as 100-fold, where their small seasonal variations (av. CV = 27%) justified respective statuses. Elevated NO₃ ^? concentrations (more than 70 µM) described a distribution of N saturation along a course of polluted air advection in the Kanto Plain. The extent of NO₃ ^? leaching from forests was not proportional to atmospheric N deposition probably because of ecosystem N retention. A dependency of NO₃ ^? level on the watershed altitude and quite constant δ¹⁵N of stream NO₃ ^? over a wide NO₃ ^? range were observed, which could be also related to this cause.