Soil N transformations after application of 15N‐labeled biomass in incubation experiments with repeated soil drying and rewetting

The effects of repeated soil drying and rewetting on microbial biomass N (N_bio) and mineral N (N_min) were measured in incubation experiments simulating typical moisture and temperature conditions for soils from temperate climates in the post‐harvest period. After application of in vitro ¹⁵N‐labeled fungal biomass to a silty loam, one set of soils was exposed to two drying‐rewetting cycles (treatment DR; 14 days to decrease soil moisture to 20 % water‐holding capacity (WHC) and subsequently 7 days at 60 % WHC). A control set (treatment CM) was kept at constant moisture conditions (60 % WHC) throughout the incubation. N_bio and N_min as well as the ¹⁵N enrichment of these N pools were measured immediately after addition of ¹⁵N‐labeled biomass (day 0) and after each change in soil moisture (day 14, 21, 35, 42). Drying and rewetting (DR) resulted in higher N_min levels compared to CM towards the end of the incubation. Considerable amounts of N_bio were susceptible to mineralization as a result of soil drying (i.e., drying enhanced the turnover of N_bio), and significantly lower N_bio values were found for DR at the end of each drying period. Immediately after biomass incorporation into the soil (day 0), 22 % of the applied ¹⁵N was found in the N_min pool. Some of this ¹⁵N_min must have been derived from dead cells of the applied microbial biomass as only about 80 % of the microbes in the biomass suspension were viable, and only 52 % of the ¹⁵N_bio was extractable (using the fumigation‐extraction method). The increase in ¹⁵N_min was higher than for unlabeled N_min, indicating that added labeled biomass was mineralized with a higher rate than native biomass during the first drying period. Overall, the effect of drying and rewetting on soil N turnover was more pronounced for treatment DR compared to CM during the second drying‐rewetting cycle, resulting in a higher flush of mineralization and lower microbial biomass N levels.     

Nitrogen turnover in a repeatedly manured arid subtropical soil: Incubation studies with 15N isotopes

Under the hot and moist conditions of irrigated agriculture in the arid subtropics, turnover of organic matter is high, which can lead to considerable carbon (C) and nitrogen (N) losses. Therefore, sustainable use of these soils requires regular manure application at high rates. To investigate the contribution of consecutive manure applications to an arid sandy soil to various soil N pools, goat manure was isotopically labeled by feeding ¹⁵N‐enriched Rhodes grass hay and applied to the soil during a two‐year field experiment. In the first year, soils received ¹⁵N‐labeled manure to distinguish between soil‐derived and manure‐derived N. In the second year, these plots were split for the application of either ¹⁵N‐labeled or unlabeled manure to discriminate N derived from previous (first year) and recent (second year) manure application. Soil samples (of control and ¹⁵N‐manured soil) were collected at the end of the first and the second year, and incubated in two laboratory experiments with labeled or unlabeled manure. At the beginning of Experiment 1, 7% of total N, 11% of K₂SO₄ extractable N, and 16% of microbial biomass N were derived from previously field‐applied manure. While the application of manure during incubation increased microbial biomass N by 225% and 410% in the control soil and the previously field‐manured soil, respectively, N₂O emissions were more affected on the control soil, releasing considerable amounts of the soil N‐pool (80% of total emissions). In Experiment 2, 4% of total N, 7% of K₂SO₄ extractable N, and 7% of microbial biomass N derived from previously applied manure, and 4%, 8%, and 3% from recently applied manure, respectively. Microbial biomass N and N₂O‐N derived from manure declined with time after manure application, whereas in Experiment 1 this tendency was only observed for microbial biomass N.     

A field study of gross rates of N mineralization and nitrification and their relationships to microbial biomass and enzyme activities in soils treated with dairy effluent and ammonium fertilizer

Abstract. Gross N mineralization and nitrification rates were measured in soils treated with dairy shed effluent (DSE) (i.e. effluent from the dairy milking shed, comprising dung, urine and water) or ammonium fertilizer (NH₄Cl) under field conditions, by injecting ¹⁵N-solution into intact soil cores. The relationships between gross mineralization rate, microbial biomass C and N and extracellular enzyme activities (protease, deaminase and urease) as affected by the application of DSE and NH₄Cl were also determined. During the first 16 days, gross mineralization rate in the DSE treated soil (4.3–6.1 μg N g^?1 soil day^?1) were significantly (P 14;< 14;0.05) higher than those in the NH₄Cl treated soil (2.6–3.4 μg N g^?1 soil day^?1). The higher mineralization rate was probably due to the presence of readily mineralizable organic substrates in the DSE, accompanied by stimulated microbial and extracellular enzyme activities. The stable organic N compounds in the DSE were slow to mineralize and contributed little to the mineral N pool during the period of the experiment. Nitrification rates during the first 16 days were higher in the NH₄Cl treated soil (1.7–1.2 μg N g^?1 soil day^?1) compared to the DSE treated soil (0.97–1.5 μg N g^?1 soil day^?1). Soil microbial biomass C and N and extracellular enzyme activities (protease, deaminase and urease) increased after the application of the DSE due to the organic substrates and nutrients applied, but declined with time, probably because of the exhaustion of the readily available substrates. The NH₄Cl application did not result in any significant increases in microbial biomass C, protease or urease activities due to the lack of carbonaceous materials in the ammonium fertilizer. However, it did increase microbial biomass N and deaminase activity. Significant positive correlations were found between gross N mineralization rate and soil microbial biomass, protease, deaminase and urease activities. Nitrification rate was significantly correlated to biomass N but not to the microbial biomass C or the enzyme activities. Stepwise regression analysis showed that the variations of gross N mineralization rate was best described by the microbial biomass C and N.     

Soil biochemical and chemical changes in relation to mature spruce (Picea abies) forest conversion and regeneration

To investigate soil changes from forest conversion and regeneration, soil net N mineralization, potential nitrification, microbial biomass N, L‐asparaginase, L‐glutaminase, and other chemical and biological properties were examined in three adjacent stands: mature pure and dense Norway spruce (Picea abies (L.) Karst) (110 yr) (stand I), mature Norway spruce mixed with young beech (Fagus sylvatica) (5 yr) (stand II), and young Norway spruce (16 yr) (stand III). The latter two stands were converted or regenerated from the mature Norway spruce stand as former. The studied soils were characterized as having a very low pH value (2.9 – 3.5 in 0.01 M CaCl₂), a high total N content (1.06 – 1.94 %), a high metabolic quotient (qCO₂) (6.7 – 16.9 g CO₂ kg^–1 h^–1), a low microbial biomass N (1.1 – 3.3 % of total N, except LOf₁ at stand III), and a relatively high net N mineralization (175 – 1213 mg N kg^–1 in LOf₁ and Of₂, 4 weeks incubation). In the converted forest (stand II), C : N ratio and qCO₂ values in the LOf₁ layer decreased significantly, and base saturation and exchangeable Ca showed a somewhat increment in mineral soil. In the regenerated forest (stand III), the total N storage in the surface layers decreased by 30 %. The surface organic layers (LOf₁, Of₂) possessed a very high net N mineralization (1.5 – 3 times higher than those in other two stands), high microbial biomass (C, N), and high basal respiration and qCO₂ values. Meanwhile, in the Oh layer, the base saturation and the exchangeable Ca decreased. All studied substrates showed little net nitrification after the first period of incubation (2 weeks). In the later period of incubation (7 – 11 weeks), a considerable amount of NO₃‐N accumulated (20 – 100 % of total cumulative mineral N) in the soils from the two pure spruce stands (I, III). In contrast, there was almost no net NO₃‐N accumulation in the soils from the converted mixed stand (II) indicating that there was a difference in microorganisms in the two types of forest ecosystems. Soil microbial biomass N, mineral N, net N mineralization, L‐asparaginase, and L‐glutaminase were correlated and associated with forest management.     

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.     

Methods for evaluating human impact on soil microorganisms based on their activity,biomass, and diversity in agricultural soils

The present review is focused on microbiological methods used in agricultural soils accustomed to human disturbance. Recent developments in soil biology are analyzed with the aim of highlighting gaps in knowledge, unsolved research questions, and controversial results. Activity rates (basal respiration, N mineralization) and biomass are used as overall indices for assessing microbial functions in soil and can be supplemented by biomass ratios (C : N, C : P, and C : S) and eco‐physiological ratios (soil organic C : microbial‐biomass C, qCO₂, qN_min). The community structure can be characterized by functional groups of the soil microbial biomass such as fungi and bacteria, Gram‐negative and Gram‐positive bacteria, or by biotic diversity. Methodological aspects of soil microbial indices are assessed, such as sampling, pretreatment of samples, and conversion factors of data into biomass values. Microbial‐biomass C (µg (g soil)^–1) can be estimated by multiplying total PLFA (nmol (g soil)^–1) by the F_PLFA‐factor of 5.8 and DNA (µg (g soil)^–1) by the F_DNA‐factor of 6.0. In addition, the turnover of the soil microbial biomass is appreciated as a key process for maintaining nutrient cycles in soil. Examples are briefly presented that show the direction of human impact on soil microorganisms by the methods evaluated. These examples are taken from research on organic farming, reduced tillage, de‐intensification of land‐use management, degradation of peatland, slurry application, salinization, heavy‐metal contamination, lignite deposition, pesticide application, antibiotics, TNT, and genetically modified plants.     

C and N turnover in structurally intact soils of different texture

The turnover of native and applied C and N in undisturbed soil samples of different texture but similar mineralogical composition, origin and cropping history was evaluated at −10 kPa water potential. Cores of structurally intact soil with 108, 224 and 337 g clay kg⁻¹ were horizontially sliced and ¹⁵N-labelled sheep faeces was placed between the two halves of the intact core. The cores together with unamended treatments were incubated in the dark at 20 °C and the evolution of CO₂-C determined continuously for 177 d. Inorganic and microbial biomass N and ¹⁵N were determined periodically. Net nitrification was less in soil amended with faeces compared with unamended soil. When adjusted for the NO₃-N present in soil before faeces was applied, net nitrification became negative indicating that NO₃-N had been immobilized or denitrified. The soil most rich in clay nitrified least N and ¹⁵N. The amounts of N retained in the microbial biomass in unamended soils increased with clay content. A maximum of 13% of the faeces ¹⁵N was recovered in the microbial biomass in the amended soils. CO₂-C evolution increased with clay content in amended and unamended soils. CO₂-C evolution from the most sandy soil was reduced due to a low content of potentially mineralizable native soil C whereas the rate constant of C mineralization rate peaked in this soil. When the pool of potentially mineralizable native soil C was assumed proportional to volumetric water content, the three soils contained similar proportions of potentially mineralizable native soil C but the rate constant of C mineralization remained highest in the soil with least clay. Thus although a similar availability of water in the three soils was ensured by their identical matric potential, the actual volume of water seemed to determine the proportion of total C that was potentially mineralizable. The proportion of mineralizable C in the faeces was similar in the three soils (70% of total C), again with a higher rate constant of C mineralization in the soil with least clay. It is hypothesized that the pool of potentially mineralizable C and C rate constants fluctuate with the soil water content.     

Role of soil drying in nitrogen mineralization and microbial community function in semi-arid grasslands of north-west Australia

We examined effects of wetting and then progressive drying on nitrogen (N) mineralization rates and microbial community composition, biomass and activity of soils from spinifex (Triodia R. Br.) grasslands of the semi-arid Pilbara region of northern Australia. We compared soils under and between spinifex hummocks and also examined impacts of fire history on soils over a 28 d laboratory incubation. Soil water potentials were initially adjusted to −100 kPa and monitored as soils dried. We estimated N mineralization by measuring changes in amounts of nitrate (NO₃⁻-N) and ammonium (NH₄⁺-N) over time and with change in soil water potential. Microbial activity was assessed by amounts of CO₂ respired. Phospholipid fatty acid (PLFA) analyses were used to characterize shifts in microbial community composition during soil drying. Net N mineralized under hummocks was twice that of open spaces between hummocks and mineralization rates followed first-order kinetics. An initial N mineralization flush following re-wetting accounted for more than 90% of the total amount of N mineralized during the incubation. Initial microbial biomass under hummocks was twice that of open areas between hummocks, but after 28 d microbial biomass was<2 μ g⁻¹ ninhydrin N regardless of position. Respiration of CO₂ from soils under hummocks was more than double that of soils from between hummocks. N mineralization, microbial biomass and microbial activity were negligible once soils had dried to −1000 kPa. Microbial community composition was also significantly different between 0 and 28 d of the incubation but was not influenced by burning treatment or position. Regression analysis showed that soil water potential, microbial biomass N, NO₃⁻-N, % C and δ¹⁵N all explained significant proportions of the variance in microbial community composition when modelled individually. However, sequential multiple regression analysis determined only microbial biomass was significant in explaining variance of microbial community compositions. Nitrogen mineralization rates and microbial biomass did not differ between burned and unburned sites suggesting that any effects of fire are mostly short-lived. We conclude that the highly labile nature of much of soil organic N in these semi-arid grasslands provides a ready substrate for N mineralization. However, process rates are likely to be primarily limited by the amount of substrate available as well as water availability and less so by substrate quality or microbial community composition.     

Short‐term effects of polyacrylamide and dicyandiamide on C and N mineralization in a sandy loam soil

The soil conditioners anionic polyacrylamide (PAM) and dicyandiamide (DCD) are frequently applied to soils to reduce soil erosion and nitrogen loss, respectively. A 27‐day incubation study was set up to gauge their interactive effects on the microbial biomass, carbon (C) mineralization and nitrification activity of a sandy loam soil in the presence or absence of maize straw. PAM‐amended soils received 308 or 615 mg PAM/kg. Nitrogen (N)‐fertilized soils were amended with 1800 mg/kg ammonium sulphate [(NH₄)₂SO₄], with or without 70 mg DCD/kg. Maize straw was added to soil at the rate of 4500 mg/kg. Maize straw application increased soil microbial biomass and respiration. PAM stimulated nitrification and C mineralization, as evidenced by significant increases in extractable nitrate and evolved carbon dioxide (CO₂) concentrations. This is likely to have been effected by the PAM improving microbial conditions and partially being utilized as a substrate, with the latter being indicated by a PAM‐induced significant increase in the metabolic quotient. PAM did not reduce the microbial biomass except in one treatment at the highest application rate. Ammonium sulphate stimulated nitrification and reduced microbial biomass; the resultant acidification of the former is likely to have caused these effects. N fertilizer application may also have induced short‐term C‐limitation in the soil with impacts on microbial growth and respiration. The nitrification inhibitor DCD reduced the negative impacts on microbial biomass of (NH₄)₂SO₄ and proved to be an effective soil amendment to reduce nitrification under conditions where mineralization was increased by addition of PAM.     

Mobile and readily available C and N fractions and their relationship to microbial biomass and selected enzyme activities in a sandy soil under different management systems

Within different land‐use systems such as agriculture, forestry, and fallow, the different morphology and physiology of the plants, together with their specific management, lead to a system‐typical set of ecological conditions in the soil. The response of total, mobile, and easily available C and N fractions, microbial biomass, and enzyme activities involved in C and N cycling to different soil management was investigated in a sandy soil at a field study at Riesa, Northeastern Germany. The management systems included agricultural management (AM), succession fallow (SF), and forest management (FM). Samples of the mineral soil (0—5, 5—10, and 10—30 cm) were taken in spring 1999 and analyzed for their contents on organic C, total N, NH₄⁺‐N and NO₃^—‐N, KCl‐extractable organic C and N fractions (Corg_(KCl) and Norg_(KCl)), microbial biomass C and N, and activities of β‐glucosidase and L‐asparaginase. With the exception of Norg_(KCl), all investigated C and N pools showed a clear relationship to the land‐use system that was most pronounced in the 0—5 cm profile increment. SF resulted in greater contents of readily available C (Corg_(KCl)), NH₄⁺‐N, microbial biomass C and N, and enzyme activities in the uppermost 5 cm of the soil compared to all other systems studied. These differences were significant at P ≤ 0.05 to P ≤ 0.001. Comparably high C_mic:C_org ratios of 2.4 to 3.9 % in the SF plot imply a faster C and N turnover than in AM and FM plots. Forest management led to 1.5‐ to 2‐fold larger organic C contents compared to SF and AM plots, respectively. High organic C contents were coupled with low microbial biomass C (78 μg g^—1) and N contents (10.7 μg g^—1), extremely low C_mic : C_org ratios (0.2—0.6 %) and low β‐glucosidase (81 μg PN g^—1 h^—1) and L‐asparaginase (7.3 μg NH₄‐N g^—1 2 h^—1) activities. These results indicate a severe inhibition of mineralization processes in soils under locust stands. Under agricultural management, chemical and biological parameters expressed medium values with exception for NO₃^—‐N contents which were significantly higher than in SF and FM plots (P ≤ 0.005) and increased with increasing soil depth. Nevertheless, the depth gradient found for all studied parameters was most pronounced in soils under SF. Microbial biomass C and N were correlated to β‐glucosidase and L‐asparaginase activity (r ≥ 0.63; P ≤ 0.001). Furthermore, microbial biomass and enzyme activities were related to the amounts of readily mineralizable organic C (i.e. Corg_(KCl)) with r ≥ 0.41 (P ≤ 0.01), suggesting that (1) KCl‐extractable organic C compounds from field‐fresh prepared soils represent an important C source for soil microbial populations, and (2) that microbial biomass is an important source for enzymes in soil. The Norg_(KCl) pool is not necessarily related to the size of microbial biomass C and N and enzyme activities in soil.<?show $6#>     

Mid-term tracing of <Superscript>15</Superscript>N derived from urine and dung in soil microbial biomass

Large amounts of C and N are returned to pasture soils by grazing animals in the form of urine and dung. Therefore, a field trial was carried out to investigate the mid-term effects of ¹⁵N-labeled excrements, produced by feeding a cow with ¹⁵N-labeled grass silage, on the soil microbial biomass. Simulating the deposition of excrements, ¹⁵N-labeled urine and dung were applied to a 0.09-m2 area of a sandy pasture soil in October 2000 and 2001. Applied amounts of N were 1,030 and 1,052 kg ha⁻¹, respectively. Soil was sampled at 0–15 cm depth, three times over 7 months and analyzed for total C and N, and microbial biomass C and N. Recovery of urine and dung N in microbial biomass was determined by ¹⁵N analysis of K₂SO₄ extracts of pre-extracted fumigated and unfumigated soils. Under dung patches, microbial biomass C was 16% and 45% higher, and microbial biomass N was 24% and 57% higher than under the untreated soil in 2001 and 2002, respectively. Under urine patches, microbial biomass C was increased after 12 weeks and decreased after 27 weeks. Microbial biomass assimilated 7% to 17% and 10% to 21% of the ¹⁵N applied initially as urine and dung, respectively. These percentages were considerably higher than those for artificially with spiked ¹⁵N urea-created and labeled manures reported in previous experiments. An important reason may be that the naturally ¹⁵N-labeled N components behave differently in soil than urea spikes.     

土壤微生物对施入肥料氮的固持及其动态研究

采集长期定位试验（１４年）土壤（棕壤）进行盆栽试验,并应用同位素＾１５Ｎ示踪技术研究了土壤中微生物对肥料氮的固持及其动态,结果表明,施肥后５天土壤微生物对施入人肥氮的固持达达到最高,除单施氮肥处理的固持量占施入人肥氮量的５．４％外,其余各处理均天１３．３％－１５．４％间,施肥后土壤微生物量氮的增加主要来自化肥氮,后者占微生物体总氮量的６４．１％－８７．３％,在作物生长期间微生物固持的化肥氮逐渐释入     

Analysis of manure and soil nitrogen mineralization during incubation

Understanding the N-cycling processes that ensue after manuring soil is essential in order to estimate the value of manure as an N fertilizer. A laboratory incubation of manured soil was carried out in order to study N mineralization, gas fluxes, denitrification, and microbial N immobilization after manure application. Four different manures were enclosed in mesh bags to allow for the separate analysis of manure and soil. The soils received 0.15 mg manure N g^–1 soil, and the microcosms were incubated aerobically and sampled throughout a 10-week period. Manure addition resulted in initial NH₄-N concentrations of 22.1 to 36.6 mg kg^–1 in the microcosms. All manured microcosms had net declines in soil mineral N. Denitrification resulted in the loss of 14.7 to 39.2% of the added manure N, and the largest N losses occurred in manures with high NH₄-N content. Increased soil microbial biomass N amounted to 6.0 to 8.6% of the added manure N. While the microcosms as a whole had negative N mineralization, all microcosms had positive net nitrification within the manure bags. Gas fluxes of N₂O and CO₂ increased in all manured soils relative to the controls. Our results show that measurement of microbial biomass N and denitrification is important to understand the fate of manure N upon soil application.     

Modelling the transformations and sequestration of soil organic matter in two contrasting ecosystems of the Andes

The mechanisms linking soil respiration to climate and soil physical properties are important for modelling transformation and sequestration of C and N in the soil. We investigated them by incubating ¹⁴C and ¹⁵N labelled straw in soils of the dry puna (Bolivian altiplano, semi‐arid shrubland at 3789 m above sea level) and the humid paramo (Venezuelan tropical alpine vegetation at 3400 m). These two ecosystems of the high Andes are comparable in terms of altitude, mean temperature and land use, but are very different regarding organic matter content, rainfall patterns and soil physical properties. Total ¹⁴C and ¹⁵N, microbial‐biomass ¹⁴C and ¹⁵N, soil moisture and meteorological data were recorded over 2 years. Daily soil moisture was predicted from a water balance model. The data from the paramo site were used to calibrate MOMOS‐6, a model of organic matter decomposition based on microbial activity and requiring only kinetic constant parameters to describe: (i) inputs to microbial biomass from plant debris and microbial metabolites, and (ii) losses from the biomass by mortality and respiration (respiration coefficient and microbial metabolic quotient qCO₂). The simulated qCO₂–¹⁴C agrees well with qCO₂–¹⁴C and qCO₂ measured at the calibration site and with published data. To apply MOMOS‐6 to the puna site, only the respiration coefficient of the biomass was re‐estimated. The dynamics of ¹⁴C and ¹⁵N were very different in the two systems. In the puna, the transformation processes stop during the long dry periods, though total annual mineralization is greater than in the paramo. The change in the value of the respiration coefficient enables us to predict that the amount of C and N sequestered in the stable humus is greater in the paramo than in the puna. The data in this paper can be used to estimate values of the respiration coefficient so that MOMOS‐6 can be applied to other systems.     

柳枝稷生物炭对来自不同地区的两种土壤上植物生物量和微生物动态的影响

Biochar amendments to soils may alter soil function and fertility in various ways, including through induced changes in the microbial community. We assessed microbial activity and community composition of two distinct clayey soil types, an Aridisol from Colorado (CO) in the U.S. Central Great Plains, and an Alfisol from Virginia (VA) in the southeastern US following the application of switchgrass (Panicum virgatum) biochar. The switchgrass biochar was applied at four levels, 0%, 2.5%, 5%, and 10%, approximately equivalent to biochar additions of 0, 25, 50, and 100 t ha^-1, respectively, to the soils grown with wheat (Triticum aestivum) in an eight-week growth chamber experiment. We measured wheat shoot biomass and nitrogen (N) content and soil nutrient availability and N mineralization rates, and characterized the microbial fatty acid methyl ester (FAME) profiles of the soils. Net N mineralization rates decreased in both soils in proportion to an increase in biochar levels, but the effect was more marked in the VA soil, where net N mineralization decreased from -2.1 to -38.4 mg kg^-1. The 10% biochar addition increased soil pH, electrical conductivity, Mehlich- and bicarbonate-extractable phosphorus (P), and extractable potassium (K) in both soil types. The wheat shoot biomass decreased from 17.7 to 9.1 g with incremental additions of biochar in the CO soil, but no difference was noted in plants grown in the VA soil. The FAME recovery assay indicated that the switchgrass biochar addition could introduce artifacts in analysis, so the results needed to be interpreted with caution. Non-corrected total FAME concentrations indicated a decline by 45% and 34% with 10% biochar addition in the CO and VA soils, respectively, though these differences became nonsignificant when the extraction efficiency correction factor was applied. A significant decline in the fungi:bacteria ratio was still evident upon correction in the CO soil with biochar. Switchgrass biochar had the potential to cause short-term negative impacts on plant biomass and alter soil microbial community structure unless measures were taken to add supplemental N and labile carbon (C).     

Rhizodeposition: Its contribution to microbial growth and carbon and nitrogen turnover within the rhizosphere

A greenhouse rhizobox experiment was carried out to investigate the fate and turnover of ¹³C‐ and ¹⁵N‐labeled rhizodeposits within a rhizosphere gradient from 0–8 mm distance to the roots of wheat. Rhizosphere soil layers from 0–1, 1–2, 2–3, 3–4, 4–6, and 6–8 mm distance to separated roots were investigated in an incubation experiment (42 d, 15°C) for changes in total C and N and that derived from rhizodeposition in total soil, in soil microbial biomass, and in the 0.05 M K₂SO₄–extractable soil fraction. CO₂‐C respiration in total and that derived from rhizodeposition were measured from the incubated rhizosphere soil samples. Rhizodeposition C was detected in rhizosphere soil up to 4–6 mm distance from the separated roots. Rhizodeposition N was only detected in the rhizosphere soils up to 3–4 mm distance from the roots. Microbial biomass C and N was increased with increasing proximity to the separated roots. Beside ¹³C and ¹⁵N derived from rhizodeposits, unlabeled soil C and N (native SOM) were incorporated into the growing microbial biomass towards the roots, indicating a distinct acceleration of soil organic matter (SOM) decomposition and N immobilization into the growing microbial biomass, even under the competition of plant growth. During the soil incubation, microbial biomass C and N decreased in all samples. Any decrease in microbial biomass C and N in the incubated rhizosphere soil layers is attributed mainly to a decrease of unlabeled (native) C and N, whereas the main portion of previously incorporated rhizodeposition C and N during the plant growth period remained immobilized in the microbial biomass during the incubation. Mineralization of native SOM C and N was enhanced within the entire investigated rhizosphere gradient. The results indicate complex interactions between substrate input derived from rhizodeposition, microbial growth, and accelerated C and N turnover, including the decomposition of native SOM (i.e., rhizosphere priming effects) at a high spatial resolution from the roots.     

Long‐lasting impact of biowaste‐compost application in agriculture on soil‐quality parameters in three different crop‐rotation systems

Soil‐quality parameters, such as soil organic matter (SOM) and plant‐available nutrient contents, microbial properties, aggregate stability, and the amounts of heavy metals were carried out in arable soils of different rotation schedules applied with a total of 50 Mg dry mass ha^–1 biowaste compost relative to an untreated control. This was investigated during a 10 y period from 1994 to 2004. Overall, soil‐quality parameters studied appeared to be promoted by biowaste‐compost application. This was evidenced for example by a remarkable increase of SOM and total N content of ≈ 15%–20% relative to the control. Subsequently, amounts of soil microbial biomass and alkaline phosphatase activity were significantly increased as well. In addition, biowaste‐compost application revealed an increase of plant‐available P and K contents and aggregate stability in soil. There was, however, no treatment effect for net N‐mineralization rates. Moreover, in soils of maize and sugar beet rotation schedule a slight decrease was found. Heavy‐metal contents of Pb and Zn were significantly increased in all compost‐treated soils, whereas no significant increase of Cd and Cu contents was measured. However, the investigated amounts were far below of the limits of the German Biowaste Ordinance. It is finally recommended, that biowaste compost may sustain and improve soil quality in agriculture when N nutrition will be considered.     

Microbial biomass and C mineralization in agricultural soils as affected by atrazine addition

This study examines the effects of atrazine on both microbial biomass C and C mineralization dynamics in two contrasting agricultural soils (organic C, texture, and atrazine application history) located at Galicia (NW Spain). Atrazine was added to soils, a Humic Cambisol (H) and a Gleyic Cambisol (G), at a recommended agronomic dose and C mineralization (CO₂ evolved), and microbial biomass measurements were made in non-treated and atrazine-treated samples at different time intervals during a 12-week aerobic incubation. The cumulative curves of CO₂–C evolved over time fit the simple first-order kinetic model [Ct = Co (1 − e ^−kt )], whose kinetic parameters were quantified. Differences in these parameters were observed between the two soils studied; the G soil, with a higher content in organic matter and microbial biomass C and lower atrazine application history, exhibited higher values of the total C mineralization and the potentially mineralizable labile C pool than those for the H soil. The addition of atrazine modified the kinetic parameters and increased notably the C mineralized; by the end of the incubation the cumulative CO₂–C values were 33–41% higher than those in the corresponding non-added soils. In contrast, a variable effect or even no effect was observed on the soil microbial biomass following atrazine addition. The data clearly showed that atrazine application at normal agricultural rates may have important implications in the C cycling of these two contrasting acid soils.     

Effect of freeze-thaw events on mineralization of soil nitrogen

Summary In humid regions of the United States there is considerable interest in the use of late spring (April–June) soil NO ₃ ^– concentrations to estimate fertilizer N requirements. However, little information is available on the environmental factors that influence soil NO ₃ ^– concentrations in late winter/early spring. The influence of freeze-thaw treatments on N mineralization was studied on several central Iowa soils. The soils were subjected to temperatures of-20°C or 5°C for 1 week followed by 0–20 days of incubation at various temperatures. The release of soluble ninhydrin-reactive N, the N mineralization rate, and net N mineralization (mineral N flush) were observed. The freeze-thaw treatment resulted in a significant increase in the N mineralization rate and mineral N flush. The N mineralization rate in the freeze-thaw treated soils remained higher than in non-frozen soils for 3–6 days when thawed soils were incubated at 25°C and for up to 20 days in thawed soils incubated at 5°C. The freeze-thaw treatments resulted in a significant release of ninhydrin-reactive N. These values were closely correlated with the mineral N flush (r ²=0.84). The release of ninhydrin-reactive N was more closely correlated with biomass N (r ²=0.80) than total N (r ²=0.65). Our results suggest that freeze-thaw events in soil disrupt microbial tissues in a similar way to drying and re-wetting or chloroform fumigation. Thus the level of mineral N released was directly related to the soil microbial biomass. We conclude that net N mineralization following a spring thaw may provide a significant portion of the total NO ₃ ^– present in the soil profile.     

Extractability of 15N-labeled corn-shoot tissue in a sandy and a clay soil by 0.01 MCaCl2 method in laboratory incubation experiments

Management of N fertilization depends not only on the mineral N measured at the beginning of the growing season but also on the status of the low-molecular-weight organic-N fraction. Our study was conducted to analyze how much of the ¹⁵N applied in labeled cornshoot tissue would be recovered in 0.01 M CaCl₂-extractable ¹⁵N fractions and wheter a decrease in the CaCl₂-extractable ¹⁵N fraction quantitatively followed the trend in net mineralization of the ¹⁵N applied in corn-shoot tissue during an incubation period. The effects of adding ¹⁵N-labeled young corn-shoot tissue to a sandy soil and a clay soil were investigated for 46 days in an aerobic incubation experiment at 25°C. The application of 80 mg N kg^-1 soil in the form of labeled corn-shoot tissue (24.62 mg ¹⁵N kg^-1 soil) resulted in a significant initial increase, followed by a decrease the labeled organic-N fraction in comparison with the untreated soils during the incubation. The labeled organic-N fraction was significantly higher in the sandy soil than in the clay soil until the 4th day of incubation. The decrease in labeled organic N in the sandy soil resulted in a subsequent increase in ¹⁵NO _inf3 ^sup- during the incubation. Ammonification of applied plant N resulted in a significant increase in the 1 M HCl-extractable non-exchangeable ¹⁵NH _inf4 ^sup+ fraction in the clay soik, owing to the vermiculite content. The ¹⁵N recovery was analyzed by the 0.01 M CaCl₂ extraction method; at the beginning of the incubation experiment, recovery was 37.0% in the sandy soil and 36.7% in the clay soil. After 46 days of incubation, recovery increased to 47.2 and 43.8% in the sandy and clay soils, respectively. Net mineralization of the ¹⁵N applied in corn-shoot tissue determined after the 46-day incubation was 6.60 mg ¹⁵N kg^-1 soil (=34.9% of the applied organic ¹⁵N) and 4.37 mg ¹⁵N kg^-1 soil (=23.1% of the applied organic ¹⁵N) in the sandy and the clay soils, respectively. The decrease in the labeled organic-N fraction extracted by 0.01 M CaCl₂ over the whole incubation period was 3.14 and 2.33 mg ¹⁵N kg^-1 soil in the sandy and clay soil, respectively. These results indicate that net mineralization of ¹⁵N was not consistent with the decrease in the labeled organic-N fraction. This may have been due to the inability of 0.01 M CaCl₂ to extract or desorb all of the applied organic ¹⁵N that was mineralized during the incubation period.