Changes in soil microbial biomass, metabolic quotient, and organic matter turnover under Hieracium (H. pilosella L.)

 In New Zealand Hieracium is an opportunistic plant that invades high country sites more or less depleted of indigenous vegetation. To understand the invasive nature of this weed we assessed the changes in soil C, N and P, soil microbial biomass C, N and P contents, microbial C : N and C : P ratios, the metabolic quotient, and turnover of organic matter in soils beneath Hieracium and its adjacent herbfield resulting from the depletion of tussock vegetation. The amounts of soil organic C and total N were higher under Hieracium by 25 and 11%, respectively, compared to soil under herbfield. This change reflects an improvement in both the quantity and quality of organic matter input to mineral soil under Hieracium, with higher percentage organic C and a lower C : N ratio. The microbial biomass C, N and P contents were also higher under Hieracium. The amount of C respired during the 34-week incubation indicated differences in the nature of soil organic matter under Hieracium, the unvegetated "halo" zone surrounding Hieracium patches, and herbfield (depleted tussock grassland). Decomposition of organic matter in these zones showed that the Hieracium soil had the greatest rate of CO₂ respired, and the halo soil had the lowest. We relate the enhanced organic C turnover to the invasive nature of Hieracium. Net N mineralization was significantly lower from the Hieracium soil (57 mg N g^–1 soil N) than from herbfield and halo soils (74 and 71 mg N g^–1 soil N, respectively), confirming that the nature of organic N in Hieracium soil is different from adjoining halo and herbfield soils. It seems plausible that specific compounds such as polyphenols and lignins released by Hieracium are not only responsible for increased organic N, but also control the form and amount of N released during organic matter transformations. We conclude that the key to the success of Hieracium in the N-deficient South Island high country of New Zealand lies in its ability to control and sequester N supply through modifying the soil organic matter cycle. Received: 1 December 1998     

Effect of cropping systems on nitrogen mineralization in soils

 Understanding the effect of cropping systems on N mineralization in soils is crucial for a better assessment of N fertilizer requirements of crops in order to minimize nitrate contamination of surface and groundwater resources. The effects of crop rotations and N fertilization on N mineralization were studied in soils from two long-term field experiments at the Northeast Research Center and the Clarion-Webster Research Center in Iowa that were initiated in 1979 and 1954, respectively. Surface soil samples were taken in 1996 from plots of corn (Zea mays L.), soybean (Glycine max (L.) Merr.), oats (Avena sativa L.), or meadow (alfalfa) (Medicago sativa L.) that had received 0 or 180 kg N ha^–1 before corn and an annual application of 20 kg P and 56 kg K ha^–1. N mineralization was studied in leaching columns under aerobic conditions at 30  °C for 24 weeks. The results showed that N mineralization was affected by cover crop at the time of sampling. Continuous soybean decreased, whereas inclusion of meadow increased, the amount of cumulative N mineralized. The mineralizable N pool (N _o) varied considerably among the soil samples studied, ranging from 137 mg N kg^–1 soil under continuous soybean to >500 mg N kg^–1 soil under meadow-based rotations, sampled in meadow. The results suggest that the N _o and/or organic N in soils under meadow-based cropping systems contained a higher proportion of active N fractions. Received: 10 February 1999     

Effects of 17-year fertilization on soil microbial biomass C and N and soluble organic C and N in loessial soil during maize growth

As labile organic pools, soluble organic matter and soil microbial biomass are sensitive to changes in soil management and therefore good indicators of soil quality. Effects of a 17-year long-term fertilization on soil microbial biomass C (SMBC) and N (SMBN), soluble organic C, and soluble organic N during the maize growing season were evaluated in a loess soil (Eum-Orthic Anthrosol) in northwest China. The fertilization treatments included no fertilizer (CK), inorganic N, P, and K fertilizer (NPK), cattle manure plus NPK fertilizer (MNPK), and straw plus NPK fertilizer (SNPK). Our results showed that C storage in the 0–20 cm soil layer was 28% to 81% higher in the fertilized treatments compared to the unfertilized treatment. In the 0–10 cm soil layer, SMBC and SMBN in the three fertilized treatments were higher than in the unfertilized treatment on all sampling dates, while microbial biomass C and N in the 0−10 cm soil layers were the highest at grain filling. In the same soil layer, soil-soluble organic C generally decreased in the order MNPK > SNPK > NPK > CK, while soluble organic N was the highest in the MNPK followed by the SNPK treatment. There was no significant difference in soluble organic N in the NPK and CK treatments throughout most of the maize growing season. Changes in soluble organic N occurred along the growing season and were more significant than those for soluble organic C. Soluble organic N was the highest at grain filling and the lowest at harvest. Overall, our results indicated that microbial biomass and soluble organic N in the surface soil were generally the highest at grain filling when maize growth was most vigorous. Significant positive relationships were found between soluble organic C and SMBC and between soluble organic N and SMBN.     

Spatial changes of soil fungal and bacterial biomass from a sub-alpine coniferous forest to grassland in a humid, sub-tropical region

 Fungal and bacterial biomass were determined across a gradient from a forest to grassland in a sub-alpine region in central Taiwan. The respiration-inhibition and ergosterol methods for the evaluation of the microbial biomass were compared. Soil fungal and bacterial biomass both significantly decreased (P<0.05) with the shift of vegetation from forest to grassland. Fungal and bacterial respiration rates (evolved CO₂) were, respectively, 89.1 μl CO₂ g^–1 soil h^–1 and 55.1 μl CO₂ g^–1 soil h^–1 in the forest and 36.7 μl CO₂ g^–1 soil h^–1 and 35.7 μl CO₂ g^–1 soil h^–1 in the grassland surface soils (0–10 cm). The fungal ergosterol content in the surface soil decreased from the forest zone (108 μg g^–1) to the grassland zone (15.9 μg g^–1). A good correlation (R ²=0.90) was exhibited between the soil fungal ergosterol content and soil fungal CO₂ production (respiration) for all sampling sites. For the forest and grassland soil profiles, microbial biomass (respiration and ergosterol) declined dramatically with depth, ten- to 100-fold from the surface organic horizon to the deepest mineral horizon. With respect to fungal to bacterial ratios for the surface soil (0–10 cm), the forest zone had a significantly (P<0.05) higher ratio (1.65) than the grassland zone (1.05). However, there was no fungal to bacterial ratio trend from the surface horizon to the deeper mineral horizons of the soil profiles. Received: 30 March 2000     

Nitrate Transformation and N2O Emission in a Typical Intensively Managed Calcareous Fluvaquent Soil: A 15-Nitrogen Tracer Incubation Study

A 56-day aerobic incubation experiment was performed with 15-nitrogen (N) tracer techniques after application of wheat straw to investigate nitrate-N (NO₃-N) immobilization in a typical intensively managed calcareous Fluvaquent soil. The dynamics of concentration and isotopic abundance of soil N pools and nitrous oxide (N₂O) emission were determined. As the amount of straw increased, the concentration and isotopic abundance of total soil organic N and newly formed labeled particulate organic matter (POM-N) increased while NO₃-N decreased. When ¹⁵NO₃-N was applied combined with a large amount of straw at 5000 mg carbon (C) kg^?1 only 1.1 ± 0.4 mg kg^?1 NO₃-N remained on day 56. The soil microbial biomass N (SMBN) concentration and newly formed labeled SMBN increased significantly (P < 0.05) with increasing amount of straw. Total N₂O-N emissions were at levels of only micrograms kg^?1 soil. The results indicate that application of straw can promote the immobilization of excessive nitrate with little emission of N₂O.     

Quantification of nitrogen excretion rates for three lumbricid earthworms using 15N

 Nitrogen excretion rates of ¹⁵N-labeled earthworms and contributions of ¹⁵N excretion products to organic (dissolved organic N) and inorganic (NH₄-N, NO₃-N) soil N pools were determined at 10  °C and 18  °C under laboratory conditions. Juvenile and adult Lumbricus terrestris L., pre-clitellate and adult Aporrectodea tuberculata (Eisen), and adult Lumbricus rubellus (Hoffmeister) were labeled with ¹⁵N by providing earthworms with ¹⁵N-labeled organic substrates for 5–6 weeks. The quantity of ¹⁵N excreted in unlabeled soil was measured after 48 h, and daily N excretion rates were calculated. N excretion rates ranged from 274.4 to 744 μg N g^–1 earthworm fresh weight day^–1, with a daily turnover of 0.3–0.9% of earthworm tissue N. The N excretion rates of juvenile L. terrestris were significantly lower than adult L. terrestris, and there was no difference in the N excretion rates of pre-clitellate and adult A. tuberculata. Extractable N pools, particularly NH₄-N, were greater in soils incubated with earthworms for 48 h than soils incubated without earthworms. Between 13 and 40% of excreted ¹⁵N was found in the ¹⁵N-mineral N (NH₄-N+NO₃-N) pool, and 13–23% was in the ¹⁵N-DON pool. Other fates of excreted ¹⁵N may have been incorporation in microbial biomass, chemical or physical protection in non-extractable N forms, or gaseous N losses. Earthworm excretion rates were combined with earthworm biomass measurements to estimate N flux from earthworm populations through excretion. Annual earthworm excretion was estimated at 41.5 kg N ha^–1 in an inorganically-fertilized corn agroecosystem, and was equivalent to 22% of crop N uptake. Our results suggest that the earthworms could contribute significantly to N cycling in corn agroecosystems through excretion processes. Received: 12 April 1999     

Extractability of microbial N as influenced by C : N ratio in the flush after drying or fumigation

 Extractability of microbial N was estimated using in situ labelling of the microbial population with ¹⁵N. Four arable soils (one grey forest soil and three chernozems with different long-term fertilization) were amended with (NH₄)₂SO₄ (unlabelled or labelled with ¹⁵N) and d-glucose with a C : N ratio of 10 : 1 or 20 : 1 for the grey forest soil and 50 : 1 for the chernozems. d-glucose and labelled N with a C : N ratio of 20 : 1 did not cause microbial immobilization of unlabelled N. The use of substrates with a C : N ratio of 50 : 1 led to a pronounced priming action on soil N and decreased the extractability of immobilized ¹⁵N. Values of the extractable biomass N fraction (k _EN ) assessed for the fumigation-extraction and rehydration procedures were similar and varied in inverse proportion to the C : N ratio of the flush. The k _EN factor was calculated using values of the C : N ratio in flushes and the fixed C : N ratio of structural cell components, with the assumption that the C : N ratio of the extractable cytoplasmic cell fraction is variable. The ratio between the extractable and non-extractable biomass N fraction (k _EC ) and the C : N ratio of non-extractable cell components were assessed as equation parameters optimized for the measured k _EN and C : N ratio of flush data. Received: 31 October 1997     

Soil respiration, nitrogen mineralization and uptake in barley following cultivation of grazed grasslands

 Soil tillage was studied as a strategy to synchronize N mineralization with plant demand following ploughing of two types of grazed pastures [ryegrass/white clover (Lolium perenne/Trifolium repens) and pure ryegrass]. The swards were either rotovated and ploughed or ploughed only. Soil respiration, as determined by a dynamic chamber method, was related to net N mineralization and to plant N uptake in a subsequent spring barley crop (Hordeum vulgare). Diurnal variations in temperature were important for the CO₂ flux and care must be taken that temperatures during measuring periods are representative of the daily mean. Soil tillage increased the CO₂ flux considerably compared with untilled soil with total emissions of 2.6 and 1.4 t C ha^–1, respectively, from start of April to end of June. Sward type or rotovation did not markedly influence accumulated emissions. Rotovation significantly increased the content of nitrate in the soil until 43 days after rotovation, showing that net N mineralization occurred rapidly during this period, in spite of low soil temperatures (5–10  °C). Rotovation increased barley grain yield by 10–12% and N-uptake by 14%. For both sward types, rotovation caused an extra N-uptake in harvested plant material of about 12 kg ha^–1. The availability of soil inorganic N at the early stages of barley was important for the final yield and N-uptake. The results indicated that soil biological activity was not enhanced by rotovation and that the yield effect of rotovation was mainly caused by quicker availability and better synchrony between N mineralization and plant uptake due to earlier start of decomposition. Received: 3 May 2000     

Influence of soil compaction on carbon and nitrogen mineralization of soil organic matter and crop residues

 We studied the influence of soil compaction in a loamy sand soil on C and N mineralization and nitrification of soil organic matter and added crop residues. Samples of unamended soil, and soil amended with leek residues, at six bulk densities ranging from 1.2 to 1.6 Mg m^–3 and 75% field capacity, were incubated. In the unamended soil, bulk density within the range studied did not influence any measure of microbial activity significantly. A small (but insignificant) decrease in nitrification rate at the highest bulk density was the only evidence for possible effects of compaction on microbial activity. In the amended soil the amounts of mineralized N at the end of the incubation were equal at all bulk densities, but first-order N mineralization rates tended to increase with increasing compaction, although the increase was not significant. Nitrification in the amended soils was more affected by compaction, and NO₃ ^–-N contents after 3 weeks of incubation at bulk densities of 1.5 and 1.6 Mg m^–3 were significantly lower (by about 8% and 16% of total added N, respectively), than those of the less compacted treatments. The C mineralization rate was strongly depressed at a bulk density of 1.6 Mg m^–3, compared with the other treatments. The depression of C mineralization in compacted soils can lead to higher organic matter accumulation. Since N mineralization was not affected by compaction (within the range used here) the accumulated organic matter would have had higher C : N ratios than in the uncompacted soils, and hence would have been of a lower quality. In general, increasing soil compaction in this soil, starting at a bulk density of 1.5 Mg m^–3, will affect some microbially driven processes. Received: 10 June 1999     

Critical sulphur concentration and sulphur requirement of microbial biomass in a glucose and cellulose-amended regosol

 The critical S concentration and S requirement of the soil microbial biomass of a granitic regosol was examined. S was applied at the rate of 0, 5, 10, 20, 30 and 50 μg S as MgSO₄·7H₂O, together with either 3000 μg glucose-C or 3333 μg cellulose-C, 400 μg N, and 200 μg P g ^–1 soil and 200 μg K g^–1 soil. Microbial biomass, inorganic SO₄ ^2–-S, and CO₂ emission were monitored over 30 days during incubation at 25  °C. Both glucose and cellulose decomposition rates responded positively to the S made available for microbial cell synthesis. The amounts of microbial biomass C and S increased with the level of applied S up to 10 μg S g^–1 soil and 30 μg S g^–1 soil in the glucose- and cellulose-amended soil, respectively, and then declined. Incorporated S was found to be concentrated within the microbial biomass or partially transformed into soil organic matter. The concentration of S in the microbial biomass was higher in the cellulose- (4.8–14.2 mg g^–1) than in the glucose-amended soil (3.7–10.9 mg g^–1). The microbial biomass C:S ratio was higher in the glucose- (46–142 : 1) than in the cellulose-amended soil (36–115 : 1). The critical S concentration in the microbial biomass (defined as that required to achieve 80% of the maximum synthesis of microbial biomass C) was estimated to be 5.1 mg g^–1 in the glucose- and 10.9 mg g^–1 in the cellulose-amended soil. The minimum requirement of SO₄ ^2–-S for microbial biomass formation was estimated to be 11 μg S g^–1 soil and 21 μg S g^–1 soil for glucose- and cellulose-amended soil, respectively. The highest levels of activity of the microbial biomass were observed at the SO₄ ^2–-S concentrations of 14 μg S g^–1 soil and 17 μg S g^–1 soil, for the glucose and cellulose amendments, respectively, and were approximately 31–54% higher during glucose than cellulose decomposition. Received: 20 October 1999     

Response of soil chemical and biological variables to small and large scale changes in climatic factors

This paper studies the effect of large- and small-scale changes of soil temperature and humidity on soil microbial biomass C and N, ergosterol, carbon utilization potential, organic and inorganic N and rate of C and N mineralization at 25°C. Large-scale variations are identified with seasonal changes in temperature and humidity. To simulate small-scale changes, soil temperature and humidity were manipulated in the field. The treatment resulted in damping of temperature fluctuations and a decrease of soil humidity.The majority of the studied variables exhibit pronounced seasonality, showing a clear-cut distinction between summer (July–August) and winter (December). In summer, C mineralization rate and carbon utilization potential was high but microbial and fungal biomass (ergosterol) was low.C and N mineralization rate and microbial and fungal biomass were only affected by sampling date, demonstrating that gross parameters of biomass and activity of microorganisms are not affected by small-scale changes in temperature and humidity. In contrast, variables relating to N availability (organic N, NH₄⁺ and NO₃⁻, microbial biomass N) and carbon utilization potential of the microbial community were highly affected by small-scale changes in soil abiotic conditions. The results suggest that changes in N dynamics induced by small-scale changes of temperature and humidity are caused by shifts in the structure of the microbial community rather than by variations in microbial biomass.     

Microbial growth rate measurements reveal that land-use abandonment promotes a fungal dominance of SOM decomposition in grazed Mediterranean ecosystems

The present study investigated the effects of land-use abandonment on the soil decomposer community of two grazed Mediterranean ecosystems (an annual grassland with scattered holm oaks and a low-density shrubland). To test the influence of grazing abandonment, a set of plots within each site were fenced and kept undisturbed during 4–5 years, during which above-ground plant community structure was monitored. After that, soil samples were collected from grazed and abandoned plots corresponding to the three different soil conditions: away from (“grass”) and below tree canopies (“oak”) within the annual grassland, and from the shrubland (“shrub”). Soil samples were split into two different layers (0–5 and 5–15 cm) and then analyzed for saprotrophic fungal (acetate into ergosterol incorporation) and bacterial (leucine incorporation) growth rates. Ergosterol content (as a fungal biomass estimator) and a standard set of soil chemistry variables were also measured. After 5 years of grazing exclusion, saprotrophic fungal growth rate clearly increased in both grass and oak surface layers whereas bacterial growth rate was not altered. This translated into significantly higher fungal-to-bacterial (F/B) growth rate ratios within the ungrazed plots. Similar trends were observed for the shrub soils after 4 years of exclusion. On the contrary, abandonment of grazing had negligible effects on the ergosterol content, as well as on the soil chemical variables (soil organic carbon, total N, C/N ratio, and pH), in all the three soil conditions assessed. These results indicated a shift toward a more fungal-dominated decomposer activity in soils following cessation of grazing and highlighted the sensitivity of the microbial growth rate parameters to changes associated with land use. Moreover, there were evidences of a faster fungal biomass turnover in the ungrazed plots, which would reflect an accelerated, though not bigger, fungal channel in soil organic matter mineralization.     

Influence of nitrogen on cellulose and lignin mineralization in blackwater and redwater forested wetland soils

 Microcosms were used to determine the influence of N additions on active bacterial and active fungal biomass, cellulose degradation and lignin degradation at 5, 10 and 15 weeks in soils from blackwater and redwater wetlands in the northern Florida panhandle. Blackwater streams contain a high dissolved organic C concentration which imparts a dark color to the water and contain low concentrations of nutrients. Redwater streams contain high concentrations of suspended clays and inorganic nutrients, such as N and P, compared to blackwater streams. Active bacterial and fungal biomass was determined by direct microscopy; cellulose and lignin degradation were measured radiometrically. The experimental design was a randomized block. Treatments were: soil type (blackwater or redwater forested wetlands) and N additions (soils amended with the equivalent of 0, 200 or 400 kg N ha^–1 as NH₄NO₃). Redwater soils contained higher concentrations of C, total N, P, K, Ca, Mn, Fe, B and Zn than blackwater soils. After N addition and 15 weeks of incubation, the active bacterial biomass in redwater soils was lower than in blackwater soils; the active bacterial biomass in blackwater soils was lower when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. The active fungal biomass in blackwater soils was higher when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. The active fungal biomass in redwater wetland soils was lower when 200 kg N ha^–1, but not when 400 kg N ha^–1, was added. Cellulose and lignin degradation was higher in redwater than in blackwater soils. After 10 and 15 weeks of incubation, the addition of 200 or 400 kg N as NH₄NO₃ ha^–1 decreased cellulose and lignin degradation in both wetland soils to similar levels. This study indicated that the addition of N may slow organic matter degradation and nutrient mineralization, thereby creating deficiencies of other plant-essential nutrients in wetland forest soils. Received: 7 April 1999     

Seasonal fluctuation in microbial biomass and activity along a natural nitrogen gradient in a drained peatland

The effects of peat total N on the dissolved N and C concentrations and microbial biomass and activity and their range of seasonal fluctuation were studied in a drained peatland forest in Finland. Seasonal fluctuations in the concentrations of extractable dissolved organic (DON) and inorganic nitrogen (DIN) compounds and extractable dissolved organic carbon (DOC), microbial C and N, ergosterol, net and gross N mineralisation rates were investigated during two growing seasons along a natural peat N gradient in a drained peatland. Significant seasonal fluctuations in NH₄⁺ and DOC concentrations, microbial C and N, but not in ergosterol or microbial C-to-N ratios in the peat, were observed during the 1999 and 2000 growing seasons. The peat total N concentration affected extractable DON and DOC, but not DIN concentrations in the peat. A negative correlation was found between total N concentration in peat and microbial N and C, and a positive correlation between total N and ergosterol, in peat with N concentrations of up to 2%. Gross mineralisation rates did not show any correlation, whereas net mineralisation rates showed a significant positive correlation with the total N concentration of the peat in both 1999 and 2000.     

Chemical and biological characteristics of alkaline saline soils from the former Lake Texcoco as affected by artificial drainage

 Soils from the former Lake Texcoco are alkaline saline and were artificially drained and irrigated with sewage effluents since the late 1980s. Undrained soil and soil drained for 1, 5 and 8 years were sampled, characterized and incubated aerobically for 90 days at 22±1  °C while production of CO₂, available P and concentrations of NH₄ ⁺, NO₂ ^– and NO₃ ^– were monitored. Artificial drainage decreased pH_H2O, water holding capacity, organic C, total N, and Na⁺, K⁺, Mg²⁺, B, Cl^– and SO₄ ^2– concentrations, increased inorganic C and Ca²⁺ concentrations more than 5-fold while total P was not affected. Microbial biomass C decreased with increased length of drainage but bacteria, actinomycetes, denitrifiers and cellulose-utilizing bacteria tended to show opposite trends. CO₂ production was less in soils drained ≥5 years compared to undrained soil but more than in soils drained for 1 year. Emission of NH₃ was negligible and concentrations of NH₄ ⁺ remained constant over time in each soil. Nitrification, as witnessed by increases in NO₃ ^– concentrations, occurred in soil drained for 8 years. NO₂ ^– concentrations decreased in soils drained ≤1 year in the first 7 days of the incubation and remained constant thereafter. It was found that artificial drainage of soils from the former Lake Texcoco profoundly affected soil characteristics. Decreases in pH and Na⁺, K⁺, Cl^– and SO₄ ^2– concentrations made conditions more favourable for plant growth, although low concentrations of inorganic N and available P might be limiting factors. Received: 1 December 1999     

Response of the soil microbial biomass and nematode population to a wetting event in nitrogen-amended Negev desert plots

 Water and N availability are the major limiting factors of primary production in desert ecosystems, and the response of soil biota to these two factors is of great importance. We examined the immediate response of soil nematodes and the microbial biomass to a single pulse of water amendment in N-treated plots in the Israeli Negev desert. Plots were treated with 0, 50 and 100 kg NH₄NO₃ ha^–1 in December 1992, and at the end of the summer period (August 1993) the plots were exposed to a 15 mm water. Soil samples from the 0–10 cm layer were collected daily and analysed soil moisture, total soluble N, nematode populations and microbial biomass. Soil moisture increased to 8.5%, then gradually decreased to 2% during the 11 days of the study. Microbial biomass, soil respiration and metabolic quotient values did not exhibit any significant correlation with soil N levels. Free-living nematode population levels in the different plots were found to increase from a mean level of 45 500 to a mean level of 92 300 individuals m^–2. N treatment was found to affect the patterns of free-living nematode population dynamics. The results of this study demonstrated the importance of moisture availability levels and the ability to mobilize previous N inputs into available N which, occurring in pulses, can affect the microbial ecophysiological status, nematode population dynamics and the interrelationship between these two important components in the desert soil milieu. Received: 5 November 1998     

Long-term winter cover cropping effects on corn (Zea mays L.) production and soil nitrogen availability

 This study was conducted to determine effects of long-term winter cover cropping with hairy vetch, cereal rye and annual ryegrass on soil N availability and corn productivity. From 1987 to 1995, with the exception of the first year of the study, the cover crops were seeded each year in late September or early October after the corn harvest and incorporated into the soil in late April or early May. Corn was seeded 10 days to 2 weeks after the cover crop residues had been incorporated, and N fertilizer was applied as a side-dressing at rates of 0, 67, 134, or 201 kg N ha^–1 each year. While the average annual total N input from the above-ground biomass of the cover crops was highest for hairy vetch (72.4 kg N ha^–1), the average annual total C input was highest for cereal rye (1043 kg C ha^–1) compared with the other cover crops. Hairy vetch was the only cover crop that significantly increased pre-side-dressed NO₃ ^–-N (N_i) corn biomass and N uptake at 0 N. At an N fertilizer rate of 134 kg N ha^–1 or higher, the cover crops had a minimal effect on corn biomass. This indicated that even after 9 years of winter cover cropping, the effect of the cover crops on corn growth resulted primarily from their influence on soil N availability. The amount of available N estimated from the cover crops (N_ac) was significantly correlated with relative corn biomass production (r ²=0.707, P<0.001). The total amount of available N, comprising N_ac and N added from fertilizer (N_f), was strongly correlated (r ²=0.820, P<0.001)) with relative corn biomass production. The correlation was also high for the available N comprising N_i and N_f (r ²=0.775, P<0.001). Although cereal rye and annual ryegrass did not improve corn biomass production in the short term, they benefited soil organic N accumulation and gradually improved corn biomass production compared with the control over the long term. Received: 10 August 1999     

Influence of nitrogen on atrazine and 2, 4 dichlorophenoxyacetic acid mineralization in blackwater and redwater forested wetland soils

 Microcosms were used to determine the influence of N additions on active bacterial and fungal biomass, atrazine and dichlorophenoxyacetic acid (2,4-D) mineralization at 5, 10 and 15 weeks in soils from blackwater and redwater wetland forest ecosystems in the northern Florida Panhandle. Active bacterial and fungal biomass was determined by staining techniques combined with direct microscopy. Atrazine and 2,4-D mineralization were measured radiometrically. Treatments were: soil type, (blackwater or redwater forested wetland soils) and N additions (soils amended with the equivalent of 0, 200 or 400 kg N ha^–1 as NH₄NO₃). Redwater soils contained higher concentrations of C, total N, P, K, Ca, Mn, Fe, B and Zn than blackwater soils. After N addition and 15 weeks of incubation, active bacterial biomass in redwater soils was lower when N was added. Active bacterial biomass in blackwater soils was lower when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. Active fungal biomass in blackwater soils was higher when 400 kg N ha^–1, but not when 200 kg N ha^–1, was added. Active fungal biomass in redwater soils was lower when 200 kg N ha^–1, but not when 400 kg N ha^–1, was added. After 15 weeks of incubation 2,4-D degradation was higher in redwater wetland soils than in blackwater soils. After 10 and 15 weeks of incubation the addition of 200 or 400 kg N ha^–1 decreased both atrazine and 2,4-D degradation in redwater soils. The addition of 400 kg N ha^–1 decreased 2,4-D degradation but not atrazine degradation in blackwater soils after 10 and 15 weeks of incubation. High concentrations of N in surface runoff and groundwater resulting from agricultural operations may have resulted in the accumulation of N in many wetland soils. Large amounts of N accumulating in wetlands may decrease mineralization of toxic agricultural pesticides. Received: 26 June 1998     

The short-term cover crops increase soil labile organic carbon in southeastern Australia

Little information is available about the effects of cover crops on soil labile organic carbon (C), especially in Australia. In this study, two cover crop species, i.e., wheat and Saia oat, were broadcast-seeded in May 2009 and then crop biomass was crimp-rolled onto the soil surface at anthesis in October 2009 in southeastern Australia. Soil and crop residue samples were taken in December 2009 to investigate the short-term effects of cover crops on soil pH, moisture, NH₄⁺–N, NO₃⁻–N, soluble organic C and nitrogen (N), total organic C and N, and C mineralization in comparison with a nil-crop control (CK). The soil is a Chromic Luvisol according to the FAO classification with 48.4 ± 2.2% sand, 19.5 ± 2.1% silt, and 32.1 ± 2.1% clay. An exponential model fitting was employed to assess soil potentially labile organic C (C ₀) and easily decomposable organic C for all treatments based on 46-day incubations. The results showed that crop residue biomass significantly decreased over the course of 2-month decomposition. The cover crop treatments had significantly higher soil pH, soluble organic C and N, cumulative CO₂–C, C ₀, and easily decomposable organic C, but significantly lower NO₃⁻–N than the CK. However, no significant differences were found in soil moisture, NH₄⁺–N, and total organic C and N contents among the treatments. Our results indicated that the short-term cover crops increased soil labile organic C pools, which might have implications for local agricultural ecosystem managements in this region.     

Impact of coastal wetland cultivation on microbial biomass, ammonia-oxidizing bacteria, gross N transformation and N2O and NO potential production

A ¹⁵N dilution experiment was carried out to investigate effects of cultivation on the gross N transformation rate in coastal wetland zone. Microbial community composition was estimated by phospholipid fatty acid (PLFA) analysis and abundance of soil ammonia-oxidizing bacteria (AOB) was quantified by real-time polymerase chain reaction (PCR). Soil salinity decreased significantly, while total N increased after coastal wetland was cultivated. Microbial biomass (total PLFA), bacterial biomass, fungal biomass, and actinomycete biomass of the native coastal wetland soils were significantly (p < 0.05) lower than those of the cultivated soils whereas AOB population size also significantly increased after coastal wetland cultivation. Multiple regression analysis showed that total PLFA biomass and soil total N (TN) explained 97% of the variation of gross N mineralization rate in the studied soils (gross mineralization rate = 0.179 total PLFA biomass + 5.828TN − 2.505, n = 16, p < 0.01). Gross nitrification rate increased by increasing the soil AOB population size and gross mineralization rate (M) (gross nitrification rate = 3.39AOB + 0.18 M − 0.075, R ² = 0.98, n = 16, p < 0.01). Management of salt discharge and mineral N fertilization during the cultivation of wetland soils might have changed composition of soil microflora and AOB population size, thus influencing mineralization and nitrification. Probably, the cultivation of coastal wetland soils increased the risk of N losses from soil through nitrate leaching and gas emission (e.g., N₂O and NO).