Effects of nickel addition on nitrogen mineralization,nitrification, and nitrogen leaching in some boreal forest soils

The effects of Ni additions on nitrification, N mineralization, and N leaching were examined in soils from boreal jack pine (Pinus banksiana Lamb.) forests. The results of a series of incubation experiments suggested that under certain conditions, Ni at 100 μg g^?1 soil can stimulate nitrification, and at 500 μg g^?1 can stimulate N mineralization. Nitrification rates were very low overall, but were higher in soils from the vicinity of the Sudbury, Ontario Ni-Cu smelters than in uncontaminated soils. The nitrifier populations, estimated by the most probable number method, were extremely low in uncontaminated soils, but also increased following some Ni additions. Increased leaching of NO_f3 ^p was observed in soil columns treated with Ni. Since N tends to be in low supply in boreal forests, and therefore tightly cycled, the observed disruptions caused by Ni inputs could have an effect on forest productivity.     

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.     

Influence of former agricultural land use on net nitrate production in forest soils

Except where nitrate is added to the soil artificially, nitrate is leached from forest soils only if it is produced. Although the factors influencing nitrification have been widely studied, nitrification activity still cannot be simply predicted from ecosystem characteristics. In France, about half of the present forest area was agricultural in 1850. Previous work suggested that former cultivation could be a major factor influencing nitrogen availability in forest soils. Using laboratory incubations, we compared the net production of ammonium and nitrate in soils from formerly manured lands planted with conifers 70–100 years ago with that in soils of surrounding ancient coniferous forests. Net nitrate production, available P content, and natural abundance of nitrogen 15, δ¹⁵N, were greater in soils from formerly manured plots than other land, whereas the C:N ratio of the soil was less. The difference in net nitrate production between previously manured sites and adjacent ancient forests was related to differences in δ¹⁵N values in the soil but not evidently to other soil properties. Because soil δ¹⁵N increases with the intensity of organic manuring, these results suggest that nitrification in forest soils depends on previous manurial practices under agriculture. In this context, the soil δ¹⁵N might be used as an indicator of both previous agricultural land use and potential nitrification. Because a significant proportion of West European forests grow on previously cultivated soils, past land use should be taken into account when evaluating the risks of nitrate leaching from forests.     

Nitrogen mineralisation in the soil of indigenous oak and pine plantation forests in a Mediterranean environment

Nitrogen mineralisation in soils of various forest sites (pine plantation, natural and thinned oak) at Uluda? University campus in Bursa, Turkey was investigated continuously over a year by the field incubation method. Net nitrogen mineralisation and nitrification rates varied depending on sampling dates. Although nitrogen mineralisation and nitrification rates increased in the spring and summer months, there was no seasonal variation in the soils of the examined forests. Annual net nitrate (NO₃^?–N) accumulation in the upper soil layer (0–5 cm) was higher in Oak I and Oak II (14 kg ha y^?1 and 12 kg ha y^?1) than in the pine plantation (8 kg ha y^?1). While annual net NO₃^?–N accumulation (0–5 cm) varied between the oak forests (possibly due to forest management practices), annual net N_min values were similar in these forests. No significant correlation was found between the examined soil parameters and net nitrification and mineralisation rates in the soils (P > 0.05). These results indicate that tree species and forest management practices play important roles in N cycling in forest ecosystems.     

Contributions of ammonia-oxidizing archaea and bacteria to nitrification in Oregon forest soils

Ammonia oxidation, the first step of nitrification, is mediated by both ammonia-oxidizing archaea (AOA) and bacteria (AOB); however, the relative contributions of AOA and AOB to soil nitrification are not well understood. In this study we used 1-octyne to discriminate between AOA- and AOB-supported nitrification determined both in soil-water slurries and in unsaturated whole soil at field moisture. Soils were collected from stands of red alder (Alnus rubra Bong.) and Douglas-fir (Pseudotsuga menziesii Mirb. Franco) at three sites (Cascade Head, the H.J. Andrews, and McDonald Forest) on acidic soils (pH 3.9–5.7) in Oregon, USA. The abundances of AOA and AOB were measured using quantitative PCR by targeting the amoA gene, which encodes subunit A of ammonia monooxygenase. Total and AOA-specific (octyne-resistant) nitrification activities in soil slurries were significantly higher at Cascade Head (the most acidic soils, pH < 5) than at either the H.J. Andrews or McDonald Forest, and greater in red alder compared with Douglas-fir soils. The fraction of octyne-resistant nitrification varied among sites (21–74%) and was highest at Cascade Head than at the other two locations. Net nitrification rates of whole soil without NH₄⁺ amendment ranged from 0.4 to 3.3 mg N kg⁻¹ soil d⁻¹. Overall, net nitrification rates of whole soil were stimulated 2- to 8-fold by addition of 140 mg NH₄⁺-N kg⁻¹ soil; this was significant for red alder at Cascade Head and the H.J. Andrews. Red alder at Cascade Head was unique in that the majority of NH₄⁺-stimulated nitrifying activity was octyne-resistant (73%). At all other sites, NH₄⁺-stimulated nitrification was octyne-sensitive (68–90%). The octyne-sensitive activity—presumably AOB—was affected more by soil pH whereas the octyne-resistant (AOA) activity was more strongly related to N availability.     

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.     

Recovery of soil organic matter,organic matter turnover and nitrogen cycling in a post-mining forest rehabilitation chronosequence

Recovery of soil organic matter, organic matter turnover and mineral nutrient cycling is critical to the success of rehabilitation schemes following major ecosystem disturbance. We investigated successional changes in soil nutrient contents, microbial biomass and activity, C utilisation efficiency and N cycling dynamics in a chronosequence of seven ages (between 0 and 26 years old) of jarrah (Eucalyptus marginata) forest rehabilitation that had been previously mined for bauxite. Recovery was assessed by comparison of rehabilitation soils to non-mined jarrah forest references sites. Mining operations resulted in significant losses of soil total C and N, microbial biomass C and microbial quotients. Organic matter quantity recovered within the rehabilitation chronosequence soils to a level comparable to that of non-mined forest soil. Recovery of soil N was faster than soil C and recovery of microbial and soluble organic C and N fractions was faster than total soil C and N. The recovery of soil organic matter and changes to soil pH displayed distinct spatial heterogeneity due to the surface micro-topography (mounds and furrows) created by contour ripping of rehabilitation sites. Decreases in the metabolic quotient with rehabilitation age conformed to conceptual models of ecosystem energetics during succession but may have been more indicative of decreasing C availability than increased metabolic efficiency. Net ammonification and nitrification rates suggested that the low organic C environment in mound soils may favour autotrophic nitrifier populations, but the production of nitrate (NO₃^?) was limited by the low gross N ammonification rates (≤1 μg N g^?1 d^?1). Gross N transformation rates in furrow soils suggested that the capacity to immobilise N was closely coupled to the capacity to mineralise N, suggesting NO₃^? accumulation in situ is unlikely. The C:N ratio of the older rehabilitation soils was significantly lower than that of the non-mined forest soils. However, variation in ammonification rates was best explained by C and N quantity rather than C:N ratios of whole soil or soluble organic matter fractions. We conclude that the rehabilitated ecosystems are developing a conservative N cycle as displayed by non-mined jarrah forests. However, further investigation into the control of nitrification dynamics, particularly in the event of further ecosystem disturbance, is warranted.     

Changes in nitrification and bacterial community structure upon cross-inoculation of Scots pine forest soils with different initial nitrification rates

Nitrification occurs slowly in many acid Scots pine forest soils. We examined if bacterial community structure and interactions between members of the bacterial community in these forest soils prohibit growth of ammonia-oxidising microorganisms and their nitrifying activity. Native and gamma-irradiated Scots pine forest soils known to have low net nitrification rates were augmented with fresh soils or soil slurries from nitrifying Scots pine forest soil, and vice versa. Augmentation of native non-nitrifying soils with nitrifying soils induced net nitrification, although no significant changes in bacterial community structure, as measured by 16S rRNA gene-based denaturing gradient gel electrophoresis (DGGE), were observed. In sterilised soils, the inoculum, i.e. native nitrifying soil or non-nitrifying soil, determined the occurrence of net nitrification and bacterial community structure, and not the origin of the sterilised soils. Our results demonstrate that low net nitrification rates in acid Scots pine forest soils cannot be (solely) explained by unfavourable abiotic soil conditions, but that still uncaptured biotic factors contribute to suppression of nitrification.     

Effects of urease inhibitors on nitrification in soils

The effects of 10 urease inhibitors on nitrification in soils were studied by determining the effects of 10 and 50 parts/10⁶ (soil basis) of each inhibitor on the amounts of nitrate and nitrite produced when soils treated with ammonium sulfate (200 μg of ammonium N/g of soil) were incubated (30°C) under aerobic conditions for 14 days. The urease inhibitors used (catechol. hydroquinone, p-benzoquinone, 2,3-dimethyl-p-benzoquinone, 2,5-dimethyl-p-benzoquinone. 2,6-dimethyl-p-benzoquinone. 2,5-dichloro-p-benzoquinone, 2,6-dichloro-p-benzoquinone. sodium p-chloromercuribenzoate, and phenylmercuric acetate) were those found most effective in previous work to evaluate more than 130 compounds as soil urease inhibitors. Their effects on nitrification were compared with those of three compounds patented as soil nitrification inhibitors (N-Serve. AM. and ST).Most of the urease inhibitors studied had little effect on nitrification when applied at the rate of 10 μg/g of soil. but had marked inhibitory effects when applied at the rate of 50 μg/g of soil. None inhibited nitrification as effectively as N-Serve. but phenylmercuric acetate inhibited nitrification more effectively than did AM or ST when applied at the rate of 10 μg/g of soil. Phenylmercuric acetate, 2,5-dimethyl-p-benzoquinone, and 2,6-dimethyl-p-benzoquinone had very marked effects on nitrification when applied at the rate of 50 μg/g of soil.     

Net nitrification rate and presence of Nitrosospira cluster 2 in acid coniferous forest soils appear to be tree species specific

The impact of four coniferous tree species and their corresponding soil factors on N transformation rates and presence of ammonia-oxidising bacteria (AOB) was studied in an acid pine forest soil (Appelscha, The Netherlands). Pine soil had a relatively low net nitrification rate, while spruce, fir and larch soils showed high net nitrification rates. 16S rRNA and amoA sequences were only found in soils with high nitrification rates and belonged solely to Nitrosospira cluster 2. We conclude that tree species, possibly through their effects on soil C/N ratios, determines the presence of Nitrosospira cluster 2. Whenever AOB are present, however, the AOB community composition appears to be similar.     

Impact of land-use types on soil nitrogen net mineralization in the sandstorm and water source area of Beijing,China

Changes of land-use type (LUT) can affect soil nutrient pools and cycling processes that relate long-term sustainability of ecosystem, and can also affect atmospheric CO₂ concentrations and global warming through soil respiration. We conducted a comparative study to determine NH₄⁺ and NO₃⁻ concentrations in soil profiles (0–200 cm) and examined the net nitrogen (N) mineralization and net nitrification in soil surface (0–20 cm) of adjacent naturally regenerated secondary forests (NSF), man-made forests (MMF), grasslands and cropland soils from the windy arid and semi-arid Hebei plateau, the sandstorm and water source area of Beijing, China. Cropland and grassland soils showed significantly higher inorganic N concentrations than forest soils. NO₃⁻-N accounted for 50–90% of inorganic N in cropland and grassland soils, while NH₄⁺-N was the main form of inorganic N in NSF and MMF soils. Average net N-mineralization rates (mg kg⁻¹ d⁻¹) were much higher in native ecosystems (1.51 for NSF soils and 1.24 for grassland soils) than in human disturbed LUT (0.15 for cropland soils and 0.85 for MMF soils). Net ammonification was low in all the LUT while net nitrification was the major process of net N mineralization. For more insight in urea transformation, the increase in NH₄⁺ and, NO₃⁻ concentrations as well as C mineralization after urea addition was analyzed on whole soils. Urea application stimulated the net soil C mineralization and urea transformation pattern was consistent with net soil N mineralization, except that the rate was slightly slower. Land-use conversion from NSF to MMF, or from grassland to cropland decreased soil net N mineralization, but increased net nitrification after 40 years or 70 years, respectively. The observed higher rates of net nitrification suggested that land-use conversions in the Hebei plateau might lead to N losses in the form of nitrate.     

Response of C and N transformations in birch soil to coniferous resin volatiles

The purpose of this study was to examine the effects of the resin volatile compounds of two coniferous tree species, Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.) on C and N transformations in soil under silver birch (Betula pendula L.). Humus layers from two study sites were used, referred here as a N-poor soil (C:N ratio 30) and a N-rich soil (C:N ratio 19.5). In addition to these, N-poor soil added with arginine was used to ensure that the soil was not N-limited. Humus layers were subjected to resin treatments during a 28-day incubation period in the laboratory. The most abundant volatile compound in both resins was α-pinene; in spruce resin β-pinene was also abundant. Resins and pure α-pinene increased CO₂-C production, i.e. C mineralization, in both soils. In contrast, net N mineralization was clearly decreased in both soils, and net nitrification was completely stopped. There was no consistent effect on soil microbial biomass C or N. Based on these results, we conclude that volatile resin compounds affect C and N transformations in soil, but the mechanism behind these effects is still unclear.     

Temporal and spatial variations in nitrogen transformations in deciduous forest ecosystems along an urban-rural gradient

Ecosystem processes such as N transformations have seldom been studied in urban and suburban areas. Here we report the temporal and spatial variations in soil N measured continuously over 16 months in remnant forests dominated by northern red oak (Quercus rubraL.) along a 130 km urban-rural transect in the New York City metropolitan area. Urban, suburban and rural forests all exhibited clear seasonal patterns in soil N concentrations and transformation rates. Concentrations of extractable inorganic N were highest in early spring, while net N mineralization and nitrification rates were highest in summer. Peak N mineralization and nitrification in urban stands tended to occur a month earlier than in rural stands. Daily net N mineralization rates averaged 4.45 mg N kg⁻¹ soil organic matter (SOM) in urban stands, 3.51 in suburban stands, and 2.49 in rural stands. In urban and suburban forests, between 23.2-73.8% of the annual net N mineralized was nitrified, but in rural forests, net nitrification was mostly below the detection limit. Annual net N mineralization rates, expressed on an areal basis (to a depth of 7.5 cm), averaged 11.6 g m⁻² in urban forests, 11.3 g m⁻² in suburban sites, and 7.3 g m⁻² in rural forests. N returns in oak litter fall were 2.15, 1.32, and 1.81 g m⁻² in urban, suburban, and rural stands, respectively. The elevated N transformation rates and nitrate production, in combination with possible pollution constraints on tree growth in urban environments, raises concern that these urban and suburban forests may be approaching an N saturated status.     

Interactions of nitrogen fertilizers and forest humus—II. Beech and oak

Laboratory incubation experiments with and without added urea or NH₄NO₃ were performed on humus from stands of beech (Fagus silvatica) grown on soils from limestone, schists, flysch and peridotites and on humus from oak (Quercus conferta) stands on soils from limestone and schists.Beech and oak humus from stands grown on soils from limestone and flysch showed considerable nitrification with a concurrent high mobilization rate of the nutrient elements Ca, Mg and K, especially in the presence of increasing urea concentrations, but no net humus N mineralization was observed. Beech humus from stands grown on soils from schists and peridotites showed no nitrification and increasing concentrations of added urea did not modify their inability to nitrify. Non-nitrifying types of humus showed considerable ammonification but their Ca, Mg and K mobilization rates were about one-tenth those observed in nitrifying humus and were inversely correlated with urea concentrations.Exchangeable Al³⁺ and extractable Mn were present in high concentrations in the underlying inorganic soils in all cases where nitrification was absent from the overlying humus but addition of 500 parts Al³⁺ and 1000 parts Mn/10⁶ separately or in combination to a nitrifying humus failed to inhibit nitrification.An interpretation of these findings is attempted with reference to the possibility of absence of nitrification in climax vegetations and the preference of certain forest species for NH⁺₄ or NO^?₃.     

N2O and NO production in various Chinese agricultural soils by nitrification

Eleven types of agricultural soils were collected from Chinese uplands and paddy fields to compare their N₂O and NO production by nitrification under identical laboratory conditions. Before starting the assays, all air-dried soils were preincubated for 4 weeks at 25 °C and 40% WFPS (water-filled pore space). The nitrification activities of soils were determined by adding (NH₄)₂SO₄ (200 mg N kg⁻¹ soil) and incubating for 3 weeks at 25 °C and 60% WFPS. The net nitrification rates obtained fitted one of two types of models, depending on the soil pH: a zero-order reaction model for acidic soils and one neutral soil (Group 0); or a first-order reaction model for one neutral soil and alkaline soils (Group 1). The results suggest that pH is the most important factor in determining the kinetics of soil nitrification from ammonium. In the Group 1 soils, initial emissions (i.e. during the first week) of N₂O and NO were 82.6 and 83.6%, respectively, of the total emissions during 3 weeks of incubation; in the Group 0 soils, initial emissions of N₂O and NO were 54.7 and 59.9%, respectively, of the total emissions. The net nitrification rate in the first week and second-third weeks were highly correlated with the initial and subsequent emissions (i.e. during the second and third weeks), respectively, of N₂O and NO. The average percentages of emitted (N₂O+NO)-N relative to net nitrification N in initial and subsequent periods were 2.76 and 0.59 for Group 0, and 1.47 and 0.44 for the Group 1, respectively. The initial and subsequent emission ratios of NO/N₂O from Group 0 (acidic) soils were 3.77 and 2.52 times, respectively, higher than those from Group 1 soils (P<0.05).     

C and N turnover of fermented residues from biogas plants in soil in the presence of three different earthworm species (Lumbricus terrestris,Aporrectodea longa,Aporrectodea caliginosa)

A soil microcosm experiment was performed to assess (1) the C- and N- turnover of residues from biogas plants in soils in the presence of three earthworm species (Lumbricus terrestris, Aporrectodea longa and Aporrectodea caliginosa) and (2) the resulting changes in soil chemical and microbiological properties when using these residues as fertilizer in comparison to conventional slurry. Earthworms were exposed in soils, fertilized with an equivalent amount of 120 kg of NH₄-N ha^?1 from: (1) conventional cattle slurry and (2) a fermented residue derived from cattle slurry, grass (silage) and maize. Additional treatments without slurry and earthworms were used as controls.There was considerable evidence that soils fertilized by fermented slurry comprised fewer amounts of readily available nutrients for microbial C and N turnover. We observed significant stimulation of microbial biomass, basal respiration and nitrification in treatments with conventional slurry, especially in the presence of earthworms. However, the stimulation of microbial activity by manure and earthworms were significantly lower in treatments with fermented slurry. Moreover, the results showed clear interactions between different earthworm species and manures. While the biomass of the anecic species (L. terrestris and A. longa) increased in both slurry treatments, the biomass of A. caliginosa (endogeic) decreased, with a significantly stronger biomass decline in treatments with fermented slurry. The metabolic quotients revealed microbial stress metabolism in fermented slurry treatments, predominantly in treatments with A. caliginosa. We conclude that particularly A. caliginosa and soil microorganisms competed for labile C sources in treatments with fermented slurry. An application of these residues as fertilizer might result in a reduction of microbial activity in agricultural soils and in a decline of endogeic earthworms.     

Soil pH and plant diversity drive co-occurrence patterns of ammonia and nitrite oxidizer in soils from forest ecosystems

In this study, we investigated how co-occurrence patters of ammonia and nitrite oxidizers, which drive autotrophic nitrification, are influenced by tree species composition as well as soil pH in different forest soils. We expected that a decline of ammonia oxidizers in coniferous forests, as a result of excreted nitrification inhibitors and at acidic sites with low availability of ammonia, would reduce the abundance of nitrite-oxidizing bacteria (NOB). To detect shifts in co-occurrence patterns, the abundance of key players was measured at 50 forest plots with coniferous respectively deciduous vegetation and different soil pH levels in the region Schwäbische Alb (Germany). We found ammonia-oxidizing archaea (AOA) and Nitrospira-like NOB (NS) to be dominating in numbers over their counterparts across all forest types. AOA co-occurred mostly with NS, while bacterial ammonia oxidizers (AOB) were correlated with Nitrobacter-like NOB (NB). Co-occurrence patterns changed from tight significant relationships of all ammonia and nitrite oxidizers in deciduous forests to a significant relationship of AOB and NB in coniferous forests, where AOA abundance was reduced. Surprisingly, no co-occurrence structures between ammonia and nitrite oxidizers could be determined at acidic sites, although abundances were correlated to the respective nitrogen pools. This raises the question whether interactions with heterotrophic nitrifiers may occur, which needs to be addressed in future studies.     

Nitrification in soils incubated with pig slurry or ammonium sulphate

The effects of temperature, moisture content and the addition of pig slurry on nitrification in two soils were studed. There was no accumulation of NO₂^?-N under the incubation conditions investigated and the accumulation of NO₃^?-N was linear for additions of 50–250 μg NH₄⁺-N g^? soil, either as ammonium sulphate or as pig slurry. Nitrate formation was treated as a single step, zero order process to enable a rate constant to be calculated. Nitrification rate increased with increasing moisture content up to the highest level tested, soil water potential ?8.0 kPa, corresponding to approximately 60% of water holding capacity in both soils. Measurable nitrification was found in both soils at the lowest moisture content (soil water potential ?1.5 MPa) and temperature (5° C) tested. The nitrification rate constant in soils treated with 50 μg NH₄⁺-N g^? soil was not significantly affected (P = 0.05) by the form of ammonium added. Addition of 250 μg NH₄⁺-N as ammonium sulphate caused a marked inhibition of nitrification at all moisture contents and temperatures. Addition of 250 μg NH₄⁺-N as pig slurry caused a marked increase in nitrification rate, the increase being greater at the higher temperatures and moisture contents.     

Kinetics of nitrification under upland and flooded soils of varying texture

Abstract

Higher rates of nitrification often reported in fine than in coarse textured soils may not be a direct effect of soil texture because in most of the earlier studies, soil water content has been usually expressed as gravimetric, volumetric or soil's water‐holding capacity without consideration of differences in density/ porosity for soils of varying texture. The same water content in texturally different soils could provide very different conditions of soil aeration and associated nitrifying activity. Effects of soil texture on nitrification was studied by incubating three semiarid subtropical soils having sandy loam, loam, and silty clay textures at 35°C for 30 days using water‐filled pore space (WFPS) as the criterion of soil aeration. Upland or aerobic soil conditions, simulated by incubating soil at 60% WFPS, exhibited very fast nitrification of added fertilizer nitrogen (N) and most of the applied 100 mg of ammonium‐nitrogen (NH₄+‐N/kg soil) was nitrified within 10 days of incubation in all three soils irrespective of the differences in texture. Under flooded soil conditions (120% WFPS), nitrification was slow and only 84 to 92% of the applied NH₄+‐N was nitrified even after 30 days. Nitrification could be described by first‐order kinetics for both the upland and flooded moisture regimes, thus nitrification rate depended upon NH₄+ concentration. At similar gravimetric water contents, rates of nitrification differed greatly in soils of varying texture, but when varying water‐holding capacity and bulk density were accounted for using WFPS, all the soils behaved similarly at 60% WFPS. Under impeded aeration (flooded conditions), however, substantial differences were observed in nitrification in soils of varying texture, the largest in fine‐textured Chamror silty clay followed by Habowal loam and the smallest in Tolewal sandy loam soil. These results illustrate the utility of WFPS, compared with soil water content, and its reliability as an indicator of aeration dependent nitrification for soils of varying texture.     

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.