Cold storage and laboratory incubation of intact soil cores do not reflect in-situ nitrogen cycling rates of tropical forest soils

Measurements of N transformation rates in tropical forest soils are commonly conducted in the laboratory from disturbed or intact soil cores. On four sites with Andisol soils under old-growth forests of Panama and Ecuador, we compared N transformation rates measured from laboratory incubation (at soil temperatures of the sites) of intact soil cores after a period of cold storage (at 5 °C) with measurements conducted in situ. Laboratory measurements from stored soil cores showed lower gross N mineralization and NH₄⁺ consumption rates and higher gross nitrification and NO₃⁻ immobilization rates than the in-situ measurements. We conclude that cold storage and laboratory incubation change the soils to such an extent that N cycling rates do not reflect field conditions. The only reliable way to measure N transformation rates of tropical forest soils is in-situ incubation and mineral N extraction in the field.     

Effects of decreasing water potential on gross ammonification and nitrification in an acid coniferous forest soil

Changes in the soil water regime, predicted as a consequence of global climate change, might influence the N cycle in temperate forest soils. We investigated the effect of decreasing soil water potentials on gross ammonification and nitrification in different soil horizons of a Norway spruce forest and tested the hypotheses that i) gross rates are more sensitive to desiccation in the Oa and EA horizon as compared to the uppermost Oi/Oe horizon and ii) that gross nitrification is more sensitive than gross ammonification. Soil samples were adjusted by air drying to water potentials from about field capacity to around −1.0 MPa, a range that is often observed under field conditions at our site. Gross rates were measured using the ¹⁵N pool dilution technique. To ensure that the addition of solute label to dry soils and the local rewetting does not affect the results by re-mineralization or preferential consumption of ¹⁵N, we compared different extraction and incubation times.T₀ times ranging from 10 to 300 min and incubation times of 48 h and 72 h did not influence the rates of gross ammonification and nitrification. Even small changes of water potential decreased gross ammonification and nitrification in the O horizon. In the EA horizon, gross nitrification was below detection limit and the response of the generally low rates of gross ammonification to decreasing water potentials was minor. In the Oi/Oe horizon gross ammonification and nitrification decreased from 37.5 to 18.3 mg N kg⁻¹ soil d⁻¹ and from 15.4 to 5.6 mg N kg⁻¹ soil d⁻¹ when the water potential decreased from field capacity to −0.8 MPa. In the Oa horizon gross ammonification decreased from 7.4 to 4.0 mg N kg⁻¹ soil d⁻¹ when the water potential reached −0.6 MPa. At such water potential nitrification almost ceased, while in the Oi/Oe horizon nitrification continued at a rather high level. Hence, only in the Oa horizon nitrification was more sensitive to desiccation than ammonification. Extended drought periods that might result from climate change will cause a reduction in gross N turnover rates in forest soils even at moderate levels of soil desiccation.     

Effects of soil moisture on gross N transformations and N2O emission in acid subtropical forest soils

Soil moisture changes, arising from seasonal variation or from global climate changes, could influence soil nitrogen (N) transformation rates and N availability in unfertilized subtropical forests. A ¹⁵?N dilution study was carried out to investigate the effects of soil moisture change (30–90 % water-holding capacity (WHC)) on potential gross N transformation rates and N₂O and NO emissions in two contrasting (broad-leaved vs. coniferous) subtropical forest soils. Gross N mineralization rates were more sensitive to soil moisture change than gross NH₄ ⁺ immobilization rates for both forest soils. Gross nitrification rates gradually increased with increasing soil moisture in both forest soils. Thus, enhanced N availability at higher soil moisture values was attributed to increasing gross N mineralization and nitrification rates over the immobilization rate. The natural N enrichment in humid subtropical forest soils may partially be due to fast N mineralization and nitrification under relatively higher soil moisture. In broad-leaved forest soil, the high N₂O and NO emissions occurred at 30 % WHC, while the reverse was true in coniferous forest soil. Therefore, we propose that there are different mechanisms regulating N₂O and NO emissions between broad-leaved and coniferous forest soils. In coniferous forest soil, nitrification may be the primary process responsible for N₂O and NO emissions, while in broad-leaved forest soil, N₂O and NO emissions may originate from the denitrification process.     

Differing N status and N retention processes of soils under old-growth lowland forest in Eastern Amazonia,Caxiuanã, Brazil

Indirect evidence of the nitrogen (N) status of tropical forests strongly suggests that in heavily weathered soils under old-growth lowland tropical forests nitrogen is in relative excess. However, within the lowland forests of the Amazon basin, there is substantial evidence that soil texture influences soil NH₄⁺ and NO₃^? concentrations and hence possibly N availability and retention in the soil. Here, we evaluate the soil N status of two heavily weathered soils which contrast in texture (sandy versus clay Oxisol). Using ¹⁵N pool dilution, we quantified gross rates of soil N cycling and retention. We also measured the δ¹⁵N signatures from the litter layer down to 50-cm depth mineral soil and calculated the overall ¹⁵N enrichment factor (ε) for each soil type. The clay soil showed high gross N mineralization and nitrification rates and a high overall ¹⁵N enrichment factor, signifying high N losses. The sandy soil had low gross rates of N cycling and ¹⁵N enrichment factor, manifesting a conservative soil N cycling. Faster turnover rates of NH₄⁺ compared to NO₃^? indicated that NH₄⁺ cycles faster through microorganisms than NO₃^?, possibly contributing to better retention of NH₄⁺ than NO₃^?. However this was opposite to abiotic retention processes, which showed higher conversion of NO₃^? to the organic N pool than NH₄⁺. Our combined results suggest that clay Oxisol in Amazonian forest have higher N availability than sandy Oxisol, which will have important consequences for changes in soil N cycling and losses when projected increase in anthropogenic N deposition will occur.     

Gross nitrogen transformations in adjacent native and plantation forests of subtropical Australia

The impact of land-use change on soil nitrogen (N) transformations was investigated in adjacent native forest (NF), 53 y-old first rotation (1R) and 5 y-old second rotation (2R) hoop pine (Araucaia cunninghamii) plantations. The ¹⁵N isotope dilution method was used to quantify gross rates of N transformations in aerobic and anaerobic laboratory incubations. Results showed that the land-use change had a significant impact on the soil N transformations. Gross ammonification rates in the aerobic incubation ranged between 0.62 and 1.78 mg N kg⁻¹ d⁻¹, while gross nitrification rates ranged between 2.1 and 6.6 mg N kg⁻¹ d⁻¹. Gross ammonification rates were significantly lower in the NF and the 1R soils than in the 2R soils, however gross nitrification rates were significantly higher in the NF soils than in the plantation soils. The greater rates of gross nitrification found in the NF soil compared to the plantation soils, were related to lower soil C:N ratios (i.e. more labile soil N under NF). Nitrification was found to be the dominant soil N transformation process in the contrasting forest ecosystems. This might be attributed to certain site conditions which may favour the nitrifying community, such as the dry climate and tree species. There was some evidence to suggest that heterotrophic nitrifiers may undertake a significant portion of nitrification.     

Gross nitrogen mineralization-, immobilization-, and nitrification rates as a function of soil C/N ratio and microbial activity

A laboratory experiment was designed to challenge the idea that the C/N ratio of forest soils may control gross N immobilization, mineralization, and nitrification rates. Soils were collected from three deciduous forests sites varying in C/N ratio between 15 and 27. They were air-dried and rewetted to induce a burst of microbial activity. The N transformation rates were calculated from an isotope dilution and enrichment procedure, in which ¹⁵NH₄Cl or Na¹⁵NO₃ was repeatedly added to the soils during 7 days of incubation. The experiments suggested that differences in gross nitrogen immobilization and mineralization rates between the soils were more related to the respiration rate and ATP content than to the C/N ratio. Peaks of respiration and ATP content were followed by high rates of mineralization and immobilization, with 1-2 days of delay. The gross immobilization of NH₄⁺ was dependent on the gross mineralization and one to two orders of magnitude larger than the gross NO₃⁻ immobilization. The gross nitrification rates were negatively related to the ATP content and the C/N ratio and greatly exceeding the net nitrification rates. Taken together, the observations suggest that leaching of nitrate from forest soils may be largely dependent on the density and activity of the microbial community.     

Temporal variations of crop residue effects on soil N transformation depend on soil properties as well as residue qualities

Purple soils (Eutric Regosols) are widely distributed in humid subtropical Southwest China. They are characterized by high nitrification activities, with risks of severe NO₃^? leaching. Incorporation of crop residues is considered an effective method to reduce NO₃^? loss. In the present study, we compared the effects of alfalfa, rice straw, and sugarcane bagasse on gross N transformation turnover in a purple soil (purple soil, pH 7.62) compared with those in an acid soil (acid soil, pH 5.26), at 12 h, 3 months, and 6 months after residue incorporation. The gross N transformation rates were determined by ¹⁵N tracing. All tested crop residues stimulated the gross N mineralization rates, but reduced the net mineralization rates in both soils at 12 h after residue incorporation; however, the extent of the effect varied with the crop residue qualities, with rice straw having the strongest effects. Crop residues reduced net nitrification rates by depressing gross autotrophic nitrification rates and stimulating NO₃^? immobilization rates in the purple soil, particularly after rice straw incorporation (net nitrification rate decreased from 16.72 mg N kg^?1 d^?1 in the control to ??29.42 mg N kg^?1 d^?1 at 12 h of residue incorporation); however, crop residues did not affect the gross autotrophic nitrification rates in the acid soil. Crop residue effects subsided almost completely within 6 months, with sugarcane bagasse showing the longest lasting effects. The results indicated that crop residues affected the N transformation rates in a temporal manner, dependent on soil properties and residue qualities.     

中国东北苹果园中土壤总硝化作用和氧化亚氮排放状况

A better understanding of nitrogen (N) transformation in agricultural soils is crucial for the development of sustainable and environmental-friendly N fertilizer management and the proposal of effective N₂O mitigation strategies. This study aimed: i) to elucidate the seasonal dynamic of gross nitrification rate and N2O emission, ii) to determine the influence of soil conditions on the gross nitrification, and iii) to confirm the relationship between gross nitrification and N₂O emissions in the soil of an apple orchard in Yantai, Northeast China. The gross nitrification rates and N₂O fluxes were examined from March to October in 2009, 2010, and 2011 using the barometric process separation (BaPS) technique and the static chamber method. During the wet seasons gross nitrification rates were 1.64 times higher than those under dry season conditions. Multiple regression analysis revealed that gross nitrification rates were significantly correlated with soil temperature and soil water-filled pore space (WFPS). The relationship between gross nitrification rates and soil WFPS followed an optimum curve peaking at 60% WFPS. Nitrous oxide fluxes varied widely from March to October and were stimulated by N fertilizer application. Statistically significant positive correlations were found between gross nitrification rates and soil N₂O emissions. Further evaluation indicated that gross nitrification contributed significantly to N₂O formation during the dry season (about 86%) but to a lesser degree during the wet season (about 51%). Therefore, gross nitrification is a key process for the formation of N₂O in soils of apple orchard ecosystems of the geographical region.     

Nitrogen turnover and N2O production in the forest floor of beech stands as influenced by forest management

Effects of forest management (thinning) on gross ammonification, net ammonification, net nitrification, microbial biomass, and N₂O production were studied in the forest floor of adjacent untreated control (“C”) and thinned (“T”) plots in three beech (Fagus sylvatica L.) stands in the Swabian Jura (Southern Germany) during three intensive field campaigns in the year 2004. The investigated sites are located less than 1 km apart on the slopes of a narrow valley. Due to different exposure (southwest, northeast, northwest), the three sites are characterized by warm‐dry microclimate (southwest site, SW) and cool‐moist microclimate (northeast site, NE; and northwest site, NW). Measurements at the NW site covered the second year (13 to 20 months) after thinning, and measurements at the SW and NE sites covered the sixth year (61 to 68 months) after thinning. Mean gross ammonification varied insignificantly across the six plots (range: 37.5 ? 31.2 to 51.0 ? 10.5 mg N (kg dry soil)^–1 d^–1). The SW site was characterized by very low net nitrification and nitrate (NO ) concentrations that were not significantly different between control and thinned plot. In contrast, for the thinned plot at the NE site (NET), significantly increased mean net nitrification (2.3 ? 1.2 mg N (kg dry soil)^–1 d^–1 at the NET plot vs. 0.4 ? 0.2 mg N (kg dry soil)^–1 d^–1 at the NEC plot) and mean extractable NO concentrations (43.9 ? 22.8 mg N (kg dry soil)^–1 at the NET plot vs. 4.1 ? 0.8 mg N (kg dry soil)^–1 at the NEC plot) were observed. The differences in net nitrification and NO concentrations across the research plots were related to differences in the forest‐floor C : N ratios: net nitrification increased exponentially below a threshold C : N value of about 25. The results of this study indicate that the forest floor of the warm‐dry SW site is very resistant to N loss triggered by thinning due to high C : N ratios around 30. Under the cool‐moist microclimate of the NE site, a significantly lower C : N ratio of 22.1 at the thinned plot (control plot: 26.7) coincided with significantly increased net nitrification. Thus, different responses of net nitrification to thinning under different microclimate appear to be triggered by different C : N ratios. Nitrous oxide production was mainly governed by forest‐floor water content, and since differences in water content at adjacent control and thinned plots were low, N₂O production was not significantly different between adjacent control and thinned plots.     

Temperature sensitivity of mineral N transformation rates, and heterotrophic nitrification: possible factors controlling the post-disturbance mineral N flush in forest floors

A major forest disturbance such as clearcutting may bring on a flush of mineral N in organic forest floor horizons, but the magnitude of this flush can vary markedly from one ecosystem to another. For example, it was previously established that clearcutting in a high elevation Engelmann spruce-subalpine fir (ESSF) ecosystem results in significantly higher NH₄⁺ and NO₃⁻ concentrations, whereas clearcutting in an old-growth coastal western hemlock (CWH) ecosystem has little effect on mineral N dynamics. We hypothesized that the higher mineral N flush observed in the ESSF ecosystem is due to a greater temperature sensitivity of mineral N transformation rates, and to a lower proportion of heterotrophic nitrifiers, compared to the CWH ecosystem. To test these two hypotheses, we sampled forest floors several times over the growing season from clearcut and old-growth plots in both ecosystems, and measured gross mineral N transformation rates at field temperatures and at 10 °C above field temperatures, as well as with and without acetylene to inhibit autotrophic nitrifiers. Gross NH₄⁺ transformations rates ranged between 20 and 120 μg N (g forest floor)⁻¹ day⁻¹ at the ESSF site, and between 15 and 40 μg N (g forest floor)⁻¹ day⁻¹ at the CWH site. Higher temperature increased gross NH₄⁺ transformation rates in forest floor samples at both sites, but the average Q₁₀ value was higher at the ESSF site (3.15) than at the CWH site (1.25). Temperature sensitivity at the ESSF site was greater in clearcut plots (Q₁₀=4.31) than in old-growth plots (Q₁₀=1.98). Gross NO₃⁻ transformation rates ranged between 10 and 32 μg N (g forest floor)⁻¹ day⁻¹ at the ESSF site, and between 10 and 24 μg N (g forest floor)⁻¹ day⁻¹ at the CWH site, but there were no significant effects of temperature or clearcutting on gross NO₃⁻ transformation rates at either site. Likewise, there were no significant differences in the proportion of heterotrophic nitrifiers between sites. Overall, our results support the view that the temperature sensitivity of microbial processes may explain the magnitude of the NH₄⁺ flush in some coniferous ecosystems, but we lack the evidence relating the magnitude of the NO₃⁻ flush to the proportion of heterotrophic nitrifiers.     

亚热带松林中强酸性土壤自养和异养硝化作用的研究

The occurrence of nitrification in some acidic forest soils is still a subject of debate. Identification of main nitrification pathways in acidic forest soils is still largely unknown. Acidic yellow soil (Oxisol) samples were selected to test whether nitrification can occur or not in acidic subtropical pine forest ecosystems. Relative contributions of autotrophs and heterotrophs to nitrification were studied by adding selective nitrification inhibitor nitrapyrin. Soil NH₄⁺-N concentrations decreased, but NO₃^--N concentrations increased significantly for the no-nitrapyrin control during the first week of incubation, indicating that nitrification did occur in the acidic subtropical soil. The calculated net nitrification rate was 0.49 mg N kg^-1 d^-1 for the no-nitrapyrin control during the first week of incubation. Nitrapyrin amendment resulted in a significant reduction of NO₃^--N concentration. Autotrophic nitrification rate averaged 0.28 mg N kg^-1 d^-1 and the heterotrophic nitrification rate was 0.21 mg N kg^-1 d^-1 in the first week. Ammonia-oxidizing bacteria (AOB) abundance increased slightly during incubation, but nitrapyrin amendment significantly decreased AOB amoA gene copy numbers by about 80%. However, the ammonia-oxidizing archaea (AOA) abundance showed significant increases only in the last 2 weeks of incubation and it was also decreased by nitrapyrin amendment. Our results indicated that nitrification did occur in the present acidic subtropical pine forest soil, and autotrophic nitrification was the main nitrification pathway. Both AOA and AOB were the active biotic agents responsible for autotrophic nitrification in the acidic subtropical pine forest soil.     

Importance of heterotrophic nitrification and dissimilatory nitrate reduction to ammonium in a cropland soil: Evidences from a 15N tracing study to literature synthesis

Future climate change is predicted to influence soil moisture regime, a key factor regulating soil nitrogen (N) cycling. To elucidate how soil moisture affects gross N transformation in a cultivated black soil, a ¹⁵N tracing study was conducted at 30%, 50% and 70% water-filled pore space (WFPS). While gross mineralization rate of recalcitrant organic N (N_rec) increased from 0.56 to 2.47 mg N kg⁻¹ d⁻¹, the rate of labile organic N mineralization declined from 4.23 to 2.41 mg N kg⁻¹ d⁻¹ with a WFPS increase from 30% to 70%. Similar to total mineralization, no distinct moisture effect was found on total immobilization of ammonium, which primarily entered the N_rec pool. Nitrate (NO₃⁻) was mainly produced via autotrophic nitrification, which was significantly stimulated by increasing WFPS. Unexpectedly, heterotrophic nitrification was observed, with the highest rate of 1.06 mg N kg⁻¹ d⁻¹ at 30% WFPS, contributing 31.8% to total NO₃⁻ production, and decreased with WFPS. Dissimilatory nitrate reduction to ammonium (DNRA) increased from near zero (30% WFPS) to 0.26 mg N kg⁻¹ d⁻¹ (70% WFPS), amounting to 16.7–92.9% of NO₃⁻ consumption. A literature synthetic analysis from global multiple ecosystems showed that the rates of heterotrophic nitrification and DNRA in test soil were comparative to the forest and grassland ecosystems, and that heterotrophic nitrification was positively correlated with precipitation, soil organic carbon (SOC) and C/N, but negatively with pH and bulk density, while DNRA showed positive relationships with precipitation, clay, SOC, C/NO₃⁻ and WFPS. We suggested that low pH and bulk density and high SOC and C/N in test soil might favor heterotrophic nitrification, and that C and NO₃⁻ availability together with anaerobic condition were crucial for DNRA. Overall, our study highlights the role of moisture in regulating gross N turnover and the importance of heterotrophic nitrification for NO₃⁻ production under low moisture and DNRA for NO₃⁻ retention under high moisture in cropland.     

Minor response of gross N turnover and N leaching to drying,rewetting and irrigation in the topsoil of a Norway spruce forest

Forest floors in the temperate climate zone are frequently subjected to strong changes in soil moisture, but the consequences for the soil N cycle are poorly known. In a field experiment we tested the hypotheses that soil drying leads to a decrease of gross N turnover and that natural rewetting causes a pulse of gross N turnover and an increase of N leaching from the forest floor. A further hypothesis was that optimal water availability induced by irrigation causes maximum N turnover and N leaching. Replicated control, throughfall exclusion and irrigation plots were established in a Norway spruce forest to simulate different precipitation patterns during a growing season. Gross N turnover rates were determined in undisturbed soil cores from Oi + Oe and Oa + EA horizons by the ¹⁵N pool dilution technique. Forest floor percolates were periodically collected by suction plates. After 142 mm throughfall was excluded, the median soil water potential at the throughfall exclusion plots increased from pF 1.9 to 4.5 in the Oi + Oe horizon and from pF 1.8 to 3.8 in the Oa + EA horizon. Gross ammonification ranged from 14 to 45 mg N kg⁻¹ soil day⁻¹ in the Oi + Oe horizon and from 4.6 to 11.4 mg N kg⁻¹ soil day⁻¹ in the Oa + EA horizon. Gross ammonification of both horizons was smallest in the throughfall exclusion plots during the manipulation, but the differences between all treatments were not statistically significant. Gross nitrification in both horizons was very small, ranging from 1.6 to 11.1 mg N kg⁻¹ soil day⁻¹. No effects of decreasing water potential and rewetting on gross nitrification rates were observed because of the small rates and huge spatial variations. Irrigation had no effect as the differences from the control in soil water potential remained small. N leaching from the forest floor was not affected by the treatments. Our findings suggest that ammonification in forest floors continues at considerable rates even at small water potentials. The hypotheses of increased N turnover and N leaching following rewetting of dry forest floor or irrigation were not confirmed.     

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.

     

好氧条件下两种水稻土的氮素总转化速率比较

Although to date individual gross N transformations could be quantified by ~(15)N tracing method and models,studies are still limited in paddy soil.An incubation experiment was conducted using topsoil(0-20 cm) and subsoil(20-60 cm) of two paddy soils,alkaline and clay(AC) soil and neutral and silt loam(NSL) soil,to investigate gross N transformation rates.Soil samples were labeled with either ~(15)NH4_NO_3 or NH_4~(15)NO_3,and then incubated at 25 °C for 168 h at 60%water-holding capacity.The gross N mineralization(recalcitrant and labile organic N mineralization) rates in AC soil were 1.6 to 3.3 times higher than that in NSL soil,and the gross N nitrification(autotrophic and heterotrophic nitrification) rates in AC soil were 2.4 to 4.4 times higher than those in NSL soil.Although gross NO_3~- consumption(i.e.,NO_3~- immobilization and dissimilatory NO_3~- reduction to NH_4~+ rates increased with increasing gross nitrification rates,the measured net nitrification rate in AC soil was approximately 2.0 to 5.1 times higher than that in NSL soil.These showed that high NO_3~- production capacity of alkaline paddy soil should be a cause for concern because an accumulation of NO_3~- can increase the risk of NO_3~- loss through leaching and denitrification.     

Conversion of grassland to coniferous woodland has limited effects on soil nitrogen cycle processes

In the last century, conversion of native North American grasslands to Juniperus virginiana forests or woodlands has dramatically altered ecosystem structure and significantly increased ecosystem carbon (C) stocks. We compared soils under recently established J. virginiana forests and adjacent native C₄-dominated grassland to assess changes in potential soil nitrogen (N) transformations and plant available N. Over a 2-year period, concentrations of extractable inorganic N were measured in soils from forest and grassland sites. Potential gross N ammonification, nitrification, and consumption rates were determined using ¹⁵N isotope-dilution under laboratory conditions, controlling for soil temperature and moisture content. Potential nitrification rates (V_max) and microbial biomass, as well as soil physical and chemical properties were also assessed. Extractable NH₄⁺ concentrations were significantly greater in grassland soils across the study period (P ≤ 0.01), but analysis by date indicated that differences in extractable inorganic N occurred more frequently in fall and winter, when grasses were senescent but J. virginiana was still active. Laboratory-based rates of gross N mineralization (ammonification) and nitrification were greater in grassland soils (P ≤ 0.05), but only on one of four dates. Potential nitrification rates (V_max) were an order of magnitude greater than gross nitrification rates in both ecosystems, suggesting that nitrification is highly constrained by NH₄⁺ availability. Differences in plant uptake of N, C inputs, and soil microclimate as forests replace grasslands may influence plant available N in the field, as evidenced by seasonal differences in soil extractable NH₄⁺, and total soil C and N accumulation. However, we found few differences in potential soil N transformations under laboratory conditions, suggesting that this grassland-to-forest conversion caused little change in mineralizable organic N pools or potential microbial activity.     

Gross N transfer rates in field soils measured by 15N-pool dilution

Abstract

A micro-plot ¹⁵N-tracer experiment was established in three different soils of a long-term soil fertility field experiment. The nutrient-poor loam sand has been subjected to various treatments over the years and this has resulted in different organic C (0.35% – 0.86%), microbial biomass (38.3 – 100.0 µg C _mic g^?1 soil), clay and fine silt contents. Using the ¹⁵N-pool dilution technique, we assessed gross N-transfer rates in the field. Gross N mineralization rates varied strongly among the three plots and ranged between 0.4 and 4.2 µg N g^?1 soil d^?1. Gross nitrification rates were estimated to be between 0 and 2.1 µg N g^?1 soil d^?1. No correlation between gross N mineralization rates and the organic matter content of the soils was established. However, gross nitrate consumption rates increased with increasing soil C content. The ¹⁵N-pool dilution technique was successfully used to measure gross N transfer rates directly in the field.     

Measuring gross nitrogen mineralization, and nitrification by 15 N isotopic pool dilution in intact soil cores

The isotope dilution method for measuring gross rates of N mineralization, immobilization, and nitrification was applied to intact soil cores so that the effects of soil mixing were avoided. Soil cores were injected with solutions of either ¹⁵NH₄⁺ or ¹⁵NO₄^?; gross mineralization rates were calculated from the decline in “N enrichment of the NH: pool during a 24-h incubation; gross nitrification rates were calculated from the decline in ¹⁵N enrichment of the NO^?₃ pool; gross rates of NH₄⁺ and NO₃^? consumption were calculated from disappearance of the ¹⁵N label. The assumptions required for application of this method to intact cores are evaluated. Sensitivity analysis revealed that homogeneous mixing of added “N with ambient pools was not a necessary assumption but that bias in distribution of added label, coincident with a non-random distribution of microbial processes, would cause significant errors in rate estimates. Rate estimates were also sensitive to errors in initial ¹⁵N and ¹⁴N pool size estimates, In a silt loam soil from a grassland site, abiotic processes consumed over 30% of the added ¹⁵NH₄⁺ within minutes of adding the label to sterilized soil. Extracting a subset of soil cores at the beginning of an incubation is recommended for obtaining initial pool size estimates. Gross immobilization is probably stimulated by addition of inorganic ¹⁵N substrate and, therefore, is overestimated by the isotope dilution method. As an alternative method, a non-linear equation is given for calculating the gross immobilization rate from the appearance of ¹⁵N in chloroform-labile microbial biomass; but incomplete extraction of biomass N may result in low estimates. Details of the isotope dilution methodology (injection rates, concentrations, experimental artefacts, etc.) are described and discussed. When care is taken to understand the underlying assumptions and sources of error, the isotope dilution method provides a powerful tool for measuring gross rates of microbial transformations of soil nitrogen in intact soil cores.     

Effect of water tension on ethylene production and consumption in montane and lowland soils in Austria

The trace gas ethylene affects plant growth and atmospheric chemistry and it interferes with soil restoration. In soil ethylene is simultaneously produced and consumed by different microorganisms. The effects of land use and soil moisture conditions on processes leading to an accumulation of ethylene are still unclear. We measured the rates at which montane and lowland soils from Austria produced and consumed ethylene over a range of water tensions and oxygen supply. Complete anaerobiosis (waterlogging, zero tension) favoured ethylene production, whereas ethylene degradation rates were greatest in soils at 30 kPa water tension. Soils from the lowland region of eastern Austria produced ethylene at rates of up to 12 pmol C₂H₄ g^–1 h^–1 under anaerobic conditions, and they consumed ethylene at rates reaching 231 pmol C₂H₄ g^–1 h^–1, after addition of 20 μl l^–1 ethylene. Deciduous forest soils consumed ethylene fastest. Ethylene formed rapidly and was also consumed rapidly in soils rich in humus and total nitrogen. Soils taken from the mountains both produced and consumed ethylene more rapidly than lowland soils did. Production rates reached 146 pmol C₂H₄ g^–1 h^–1 under anaerobic conditions. Spruce forest soils produced significantly more ethylene than pastures. Ethylene formation was negatively correlated with soil pH. In montane soils ethylene production was related to the availability of simple carbon sources, expressed by the amount of extractable glucose equivalents. Maximum ethylene degradation amounted to 895 pmol g^–1 h^–1. Most of the soils were net sinks for ethylene at a water tension of 30 kPa and drier.