Relationship between rimsulfuron degradation and microbial biomass content in a clay loam soil

 The present research was conducted to determine the relationship between the degradation of rimsulfuron and soil microbial biomass C in a laboratory-incubated clay loam soil (pH=8.1; organic matter=2.1%) under different conditions and at different initial dosages (field rate, 10 and 100 times the field rate). The half-life values varied between 0.4 and 103.4 days depending on temperature, soil moisture and initial dose. Evidence suggested that rimsulfuron could pose environmental risks in cold and dry climatic conditions. Significant decreases in microbial biomass C content in rimsulfuron-treated soil, compared to untreated soil, were observed initially, especially at higher temperatures and low moisture levels, but never exceeded 20.3% of that in control soil. The microbial biomass C content then returned to initial values at varying times depending on incubation conditions. The relationship between herbicide degradation and microbial biomass C content gave parabolic curves (P<0.005 in all cases) under all conditions tested. Generally, maximum biomass C decrease coincided with the decrease in the concentration of rimsulfuron to about 50% of the initial dose, except at 10  °C and 100×, when biomass began to recover as early as 65–70% of the initial dose. The final equations could be useful to deduce the decrease of soil microbial biomass in relation to herbicide concentration. From the degradation kinetics of the herbicide, the time required to reach this decrease can also be calculated. Received: 19 July 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     

Seasonal changes of microbial biomass carbon related to climatic factors in soils from karst areas of southwest China

 The seasonal responses of soil microbial biomass C to changes in atmospheric temperature, soil moisture and soluble organic C were studied in soils from the karst areas of southwest China. These soils are relatively weathered, leached and impoverished, and have a low input of plant residues. Over 1 year, an inverse relationship between soil microbial biomass C and atmospheric temperature was found. The highest microbial biomass C occurred in winter and the lowest in summer, and ranged from 231–723 μg g^–1 dry soil. Although there was no obvious relationship between microbial biomass C and soil moisture, a negative correlation existed between microbial biomass C and soluble organic C. In the ecosystem studied, the marked changes in soil microbial biomass C at above 20  °C were ascribed to fluctuations of soil moisture, which were controlled by climatic factors and geomorphic conditions. The patterns of soluble organic C turnover were similar to those of soluble carbohydrate C, both of which were controlled by soil drying-rewetting cycles. It was concluded that the lowest amounts of soil microbial biomass C, measured in the summer, resulted in increases in soluble organic C due to higher turnover rates of the former at warmer air temperatures. Thus, there was a marked seasonal change in soil microbial biomass C. Received: 1 November 1998     

Combined effect of biochar and soil moisture on soil chemical properties and microbial community composition in microplastic-contaminated agricultural soil

Accumulation of microplastics (MPs) in agricultural environments has caused growing concern in recent years because of its detrimental impacts on soil quality, crop productivity and ecosystem function. This study was conducted to assess the impact of biochar on soil chemical and microbial properties in a MP-contaminated soil under two moisture regimes. Soil was contaminated with 1% (w/w) of low-density polyethylene MPs. Four types of standard biochar, that is, oil seed rape (OSR) biochar produced at 550°C (OSR 550) and 700°C (OSR 700) and soft wood pellet (SWP) biochar produced at 550°C (SWP 550) and 700°C (SWP 700), were applied at a rate of 5% (w/w). The control was maintained without MP addition. The samples were incubated in soil with two moisture regimes, that is, at 30% and 70% of the water holding capacity, and the soil chemical and microbiological properties were assessed after 100 days of incubation. OSR biochar application significantly increased soil pH (8.53–8.81) and electrical conductivity (0.51–0.58 dS/m) in both moisture regimes. The effect of biochar application on soil enzyme activity and microbial community composition did not show a clear trend. However, SWP 700 biochar improved soil enzyme activity compared with that of the control and improved bacterial diversity and evenness compared with those of other biochars, which was attributed to the high surface area available for microbial colonization. Low soil moisture content significantly reduced enzyme activity and bacterial richness even with biochar amendment, except for SWP 550 biochar. This study implies the suitability of biochar for improvement of soil quality in MP contaminated soil under both moisture regimes. However, further long-term studies are needed to get a clear understanding on the impact of different types of biochar on MP-contaminated soil.     

Microwave irradiation of soil for routine measurement of microbial biomass carbon

 Microwave irradiation was evaluated as a non-toxic alternate to chloroform fumigation for routine measurement of soil microbial biomass C. Microwave energy was applied to moist soil to disrupt microbial cells. The flush of C released was then measured after extraction or incubation. Microwave irradiation at 800 J g^–1 soil was optimal because this level resulted in an almost instantaneous rise in soil temperature (≥80  °C), an abrupt reduction in microbial activity, maximal release of biomass C, and minimal solubilization of humic substances. Both incubation-CO₂ titration and extraction-colorimetry methods were used on separate 20-g subsamples to compare the labile C in the microwave-treated and untreated soil samples. The incubation-titration method was also used to measure C in chloroform-fumigated soil samples. Averaged across soils, the chloroform fumigation yielded 123.3±5.1 mg CO₂-C kg^–1. Microwave irradiation yielded 93.6±3.9 mg CO₂-C kg^–1 soil determined by incubation and 52.4±2.4 mg C kg^–1 soil determined by extraction, accounting for 76% and 42% of the net flush of C measured by the chloroform fumigation. Microwave-stimulated net flushes of C were correlated closely (r ²=0.974 for incubation or 0.908 for extraction) with microbial biomass C measured by the chloroform fumigation. Little correlation was found with the total soil organic C (r ²=0.241 for incubation or for 0.166 extraction). Mean efficiency factors for incubation (K _MI) or extraction (K _ME) were used to calculate microbial biomass C from net flushes of C between microwaved and unmicrowaved soils. Values of K _MI and K _ME were not affected by soil pH, bulk density or clay contents. Extraction of microwaved soil by 0.5M K₂SO₄ proved to be a simple, fast, precise, reliable, and safe method to measure soil microbial biomass C. Received: 12 September 1997     

Significance of temperature and water availability for soil phosphorus transformation and microbial community composition as affected by fertilizer sources

Little is known about the effects of temperature and drying–rewetting on soil phosphorus (P) fractions and microbial community composition in regard to different fertilizer sources. Soil P dynamics and microbial community properties were evaluated in a soil not fertilized or fertilized with KH₂PO₄ or swine manure at two temperatures (10 and 25 °C) and two soil water regimes (continuously moist and drying–rewetting cycles) in laboratory microcosm assays. The P source was the dominant factor determining the sizes of labile P fractions and microbial community properties. Manure fertilization increased the content of labile P, microbial biomass, alkaline phosphomonoesterase activity, and fatty acid contents, whereas KH₂PO₄ fertilization increased the content of labile inorganic P and microbial P. Water regimes, second to fertilization in importance, affected more labile P pools, microbial biomass, alkaline phosphomonoesterase activity, and fatty acid contents than temperature. Drying–rewetting cycles increased labile P pools, decreased microbial biomass and alkaline phosphomonoesterase activity, and shaped the composition of microbial communities towards those with greater percentages of unsaturated fatty acids, particularly at 25 °C in manure-fertilized soils. Microbial C and P dynamics responded differentially to drying–rewetting cycles in manure-fertilized soils but not in KH₂PO₄-fertilized soils, suggesting their decoupling because of P sources and water regimes. Phosphorus sources, temperature, and water regimes interactively affected the labile organic P pool in the middle of incubation. Overall, P sources and water availability had greater effects on P dynamics and microbial community properties than temperature.     

Nitrous oxide emissions from a fallow and wheat field as affected by increased soil temperatures

 In order to determine the effects of increased soil temperature resulting from global warming on microbiological reactions, a 21-month field experiment was carried out in the Bavarian tertiary hills. The major objective was to focus on N₂O releases as either a positive or negative feedback in response to global warming. The soils of a fallow field and a wheat field were heated 3  °C above ambient temperature and N₂O fluxes were measured weekly from June 1994 to March 1996. During the experimental period, measured temperature differences between the control plots and the heated plots were 2.9±0.3  °C at a depth of 0.01 m and 1.0–1.8  °C at a depth of 1 m. Soil moisture decreased with the elevated soil temperatures of the heated plots. The mean differences in soil moisture between the treatments were 6.4% (fallow field) and 5.2%_DW (wheat field dry weight, DW), respectively. Overall N₂O releases during the experimental period from the fallow field were 4.8 kg N₂O–N ha^–1 in the control plot against 5.0 kg N₂O–N ha^–1 in the heated plot, and releases from the wheat field were 8.0 N₂O–N ha^–1 in the control plot and 7.6 N₂O–N kg ha^–1 in the heated plot. However, on a seasonal basis, cumulated N₂O emissions differed between the plots. During the summer months (May–October), releases from the heated fallow plot were 3 times the rates from the control plot. In the winter months, N₂O releases increased in both the fallow and wheat fields and were related to the number of freezing and thawing cycles. Received: 1 December 1997     

Experimental warming effects on the microbial community of a temperate mountain forest soil

Soil microbial communities mediate the decomposition of soil organic matter (SOM). The amount of carbon (C) that is respired leaves the soil as CO₂ (soil respiration) and causes one of the greatest fluxes in the global carbon cycle. How soil microbial communities will respond to global warming, however, is not well understood. To elucidate the effect of warming on the microbial community we analyzed soil from the soil warming experiment Achenkirch, Austria. Soil of a mature spruce forest was warmed by 4 °C during snow-free seasons since 2004. Repeated soil sampling from control and warmed plots took place from 2008 until 2010. We monitored microbial biomass C and nitrogen (N). Microbial community composition was assessed by phospholipid fatty acid analysis (PLFA) and by quantitative real time polymerase chain reaction (qPCR) of ribosomal RNA genes. Microbial metabolic activity was estimated by soil respiration to biomass ratios and RNA to DNA ratios. Soil warming did not affect microbial biomass, nor did warming affect the abundances of most microbial groups. Warming significantly enhanced microbial metabolic activity in terms of soil respiration per amount of microbial biomass C. Microbial stress biomarkers were elevated in warmed plots. In summary, the 4 °C increase in soil temperature during the snow-free season had no influence on microbial community composition and biomass but strongly increased microbial metabolic activity and hence reduced carbon use efficiency.     

Gross nitrogen mineralization and nitrification rates and their relationships to enzyme activities and the soil microbial biomass in soils treated with dairy shed effluent and ammonium fertilizer at different water potentials

 Gross N mineralization and nitrification rates and their relationships to microbial biomass C and N and enzyme (protease, deaminase and urease) activities were determined in soils treated with dairy shed effluent (DSE) or NH₄ ⁺ fertilizer (NH₄Cl) at a rate equivalent to 200 kg N ha^–1 at three water potentials (0, –10 and –80 kPa) at 20  °C using a closed incubation technique. After 8, 16, 30, 45, 60 and 90 days of incubation, sub-samples of soil were removed to determine gross N mineralization and nitrification rates, enzyme activities, microbial biomass C and N, and NH₄ ⁺ and NO₃ ^– concentrations. The addition of DSE to the soil resulted in significantly higher gross N mineralization rates (7.0–1.7 μg N g^–1 soil day^–1) than in the control (3.8–1.2 μg N g^–1 soil day^–1), particularly during the first 16 days of incubation. This increase in gross mineralization rate occurred because of the presence of readily mineralizable organic substrates with low C : N ratios, and stimulated soil microbial and enzymatic activities by the organic C and nutrients in the DSE. The addition of NH₄Cl did not increase the gross N mineralization rate, probably because of the lack of readily available organic C and/or a possible adverse effect of the high NH₄ ⁺ concentration on microbial activity. However, nitrification rates were highest in the NH₄Cl-treated soil, followed by DSE-treated soil and then the control. Soil microbial biomass, protease, deaminase and urease activities were significantly increased immediately after the addition of DSE and then declined gradually with time. The increased soil microbial biomass was probably due to the increased available C substrate and nutrients stimulating soil microbial growth, and this in turn resulted in higher enzyme activities. NH₄Cl had a minimal impact on the soil microbial biomass and enzyme activities, possibly because of the lack of readily available C substrates. The optimum soil water potential for gross N mineralization and nitrification rates, microbial and enzyme activities was –10 kPa compared with –80 kPa and 0 kPa. Gross N mineralization rates were positively correlated with soil microbial biomass N and protease and urease activities in the DSE-treated soil, but no such correlations were found in the NH₄Cl-treated soil. The enzyme activities were also positively correlated with each other and with soil microbial biomass C and N. The forms of N and the different water potentials had a significant effect on the correlation coefficients. Stepwise regression analysis showed that protease was the variable that most frequently accounted for the variations of gross N mineralization rate when included in the equation, and has the potential to be used as one of the predictors for N mineralization. Received: 10 March 1998     

Relationship between soil neutral sugar composition and the amount of labile soil organic matter in Andisol treated with bark compost or leaf litter

 The effect of short-term bark compost (Ba) and leaf litter (Li) applications on the labile soil organic matter (SOM) status was investigated. The SOM status studied in this paper includes soil microbial biomass, soil available N, hot water extractable C (HwC) and N (HwN) and soil neutral sugar-C composition. The soil microbial biomass C (MBC) and N (MBN), soil available N, HwC and HwN increased upon application of Ba and Li. No quantitative relationship was observed between application of organic material and MBC, MBN or soil available N. A positive linear correlation was observed between MBN and HwC but not between MBN and soil available N. Among the various soil neutral sugar C, xylose C (Xyl) content in Ba plots showed a remarkable increase but mannose C (Man) did not differ among Fer (fertilizer), Ba or Li plots. Soil neutral sugar C had a positive linear correlation with soil available N, MBN and HwC. The proportion of MBN : TN is positively correlated with the Xyl/Man ratio. The increase in the proportion of MBN in SOM seems to occur with the increase of SOM derived from plant debris. Received: 20 October 1997     

Phosphorus mineralization and microbial biomass in a Florida Spodosol: effects of water potential, temperature and fertilizer application

 Phosphorus mineralization and microbial biomass were measured in the surface 5 cm of a Spodosol (sandy, siliceous hyperthermic Ultic Alaquod) from north-central Florida. Soils from fertilized and unfertilized plantations of loblolly pine (Pinus taeda L.) were incubated at a range of water potentials (∼0, –3, –8, –10 and –1500 kPa) and temperatures (15  °C, 25  °C and 38  °C) for 14 days and 42 days. Increasing water potential and temperature increased specific P mineralization (mineralization expressed as a percentage of total P) regardless of fertilizer treatment. An increase in water potential from –10 kPa to –0.1 kPa resulted in an increase of between 38% and 239% in the concentration of KCl-extractable inorganic P, depending on incubation temperature and time. An increase in incubation temperature from 15  °C to 38  °C resulted in an increase of between 13% and 53% in KCl-extractable inorganic P. Changes in specific P mineralization with change in water potential or temperature were not affected by fertilizer application. This suggests that, although specific P mineralization was greater in the fertilized soils, environmental control of P mineralization was the same for both treatments. Specific P mineralization was most sensitive when soils were at higher water potentials, and decreased logarithmically to water potentials of between –3 kPa and –8 kPa. Specific P mineralization was relatively insensitive to changes in water potential when water potential was lower than –8 kPa. Microbial biomass C showed no consistent responses to changes of temperature or water potential and was not significantly correlated with specific P mineralization. Our results suggest that field estimates of P mineralization in these Spodosols may be improved by accounting for changes in soil water potential and temperature. Received: 30 October 1997     

Short-term effects of thinning on soil respiration in a pine (Pinus tabulaeformis) plantation

Respiration was measured at daytime during the growing seasons (May–October) of 2011 and 2012 in a young Pinus tabulaeformis plantation with heavy, medium and light intensity thinning and unthinned control plots in Shanxi province in northern China. Soil temperature, moisture, fine root biomass, amounts of soil organic C and litterfall biomass were also measured. We found that immediately following thinning treatments, soil respiration increased by 8 %–21 % compared with the unthinned control plots during both growing seasons. Thinning significantly affected soil respiration and soil temperature with different thinning intensities, while there were no significant differences in soil moisture among the various treatments. During the growing seasons, the soil respiration rates were positively correlated with the soil moisture: the 19.4 %–54.0 % variation in soil respiration rates in the four thinning regimes are explained by the changes in soil moisture. Meanwhile, a positive correlation was found between soil temperature and soil respiration rates at all sites. The best fitting model with temperature and moisture explained 44.3 % of the variation in soil respiration in the high thinning treatment, 27.6 % in the light thinning treatment, 18.6 % in medium thinning and in the control sites during the measuring periods. Overall, soil respiration is better predicted by soil moisture, soil organic C, live fine root biomass and soil temperature when data are pooled for all thinning treatments over the two growing seasons. The best regression model explained 74.7 % of the total variation in soil respiration over the different thinning intensities for the two sampling periods.     

Einfluß variierter Temperatur und Feuchte auf mikrobielle Aktivitäten im Boden unter Laborbedingungen

Influence of varied soil temperature and moisture on microbial activities under laboratory conditions Under laboratory conditions the influence of temperature (10°C, 20°C, fluctuation from 5° to 30°C within 12 h with additional freezing for 3 days) and soil moisture (30%, 60% w.h.c., remoistening to 60% for 1 week) on several microbial activities was investigated. The biomass-related, glucose-induced short-term respiration and the dehydrogenase activity (TTC reduction) were higher at 10°C in most cases as compared to 20°C. Independent of freezing fluctuating temperature caused the lowest activities. The nitrogen mineralization (including nitrification), however, was affected in the opposite way. No marked influences were observed with β-glucosidase, arylsulfatase, and alkaline phosphatase. In the sandy loam nearly no effects of the soil moisture occurred and in the loamy sand especially the dehydrogenase activity was higher at 30% w.h.c., whereas the nitrogen mineralization was lower. From the results it can be concluded, that ecological conditions favouring mineralization without substrate addition may even reduce microbial biomass by decomposition.     

Determination of the soil microbial biomass carbon using the method of substrate-induced respiration

Specific features of determining the carbon content in the soil microbial biomass using the method of substrate-induced respiration (MB_SIR) were studied as related to the conditions of the incubation (the glucose concentration and temperature) and pre-incubation (the duration and temperature) of the soil samples collected in the summer (tundra gley and soddy-podzolic soils and chernozems) and in different seasons (for the gray forest soil). The glucose concentration providing the highest substrate-induced respiration (SIR) in the soils studied was shown to be 2–15 mg/g. The MB_SIR in the soil samples collected in summer and in the soils pre-incubated for 10 and 22°C (7 days) did not significantly differ. The MB_SIR in the gray forest soil pre-incubated at 3, 6, and 10°C (winter, spring/autumn, and summer, respectively) and at 22°C (recommended by the authors of the SIR method) was similar for the cropland in all the seasons. For the meadow, it was the same in the winter, summer, and autumn, and, in summer, it did not differ only for the forest. For the comparative assessment of the MB_SIR, soil samples from different ecosystems are recommended to be collected in the autumn or in the summer. Soil samples of 100–500 g should be pre-incubated for 7 days at 22°C and moisture of 60% of the total water capacity; then, 1-2 g soil should be incubated with glucose (10 mg/g) at 22°C for 3–5 hours.     

Organic matter dynamics in a temperate forest as influenced by soil frost

In the future, climate models predict an increase in global surface temperature and during winter a changing of precipitation from less snowfall to more raining. Without protective snow cover, freezing can be more intensive and can enter noticeably deeper into the soil with effects on C cycling and soil organic matter (SOM) dynamics. We removed the natural snow cover in a Norway spruce forest in the Fichtelgebirge Mts. during winter from late December 2005 until middle of February 2006 on three replicate plots. Hence, we induced soil frost to 15 cm depth (at a depth of 5 cm below surface up to –5°C) from January to April 2006, while the snow‐covered control plots never reached temperatures < 0°C. Quantity and quality of SOM was followed by total organic C and biomarker analysis. While soil frost did not influence total organic‐C and lignin concentrations, the decomposition of vanillyl monomers (Ac/Ad)_V and the microbial‐sugar concentrations decreased at the end of the frost period, these results confirm reduced SOM mineralization under frost. Soil microbial biomass was not affected by the frost event or recovered more quickly than the accumulation of microbial residues such as microbial sugars directly after the experiment. However, in the subsequent autumn, soil microbial biomass was significantly higher at the snow‐removal (SR) treatments compared to the control despite lower CO₂ respiration. In addition, the water‐stress indicator (PLFA [cy17:0 + cy19:0] / [16:1ω7c + 18:1ω7c]) increased. These results suggest that soil microbial respiration and therefore the activity was not closely related to soil microbial biomass but more strongly controlled by substrate availability and quality. The PLFA pattern indicates that fungi are more susceptible to soil frost than bacteria.     

Tebuconazole application decreases soil microbial biomass and activity

A short-term mesocosm experiment was conducted to ascertain the impact of tebuconazole on soil microbial communities. Tebuconazole was applied to soil samples with no previous pesticide history at three rates: 5, 50 and 500 mg kg⁻¹ DW soil. Soil sampling was carried out after 0, 7, 30, 60 and 90 days of incubation to determine tebuconazole concentration and microbial properties with potential as bioindicators of soil health [i.e., basal respiration, substrate-induced respiration, microbial biomass C, enzyme activities (urease, arylsulfatase, β-glucosidase, alkaline phosphatase, dehydrogenase), nitrification rate, and functional community profiling]. Tebuconazole degradation was accurately described by a bi-exponential model (degradation half-lives varied from 9 to 263 days depending on the concentration tested). Basal respiration, substrate-induced respiration, microbial biomass C and enzyme activities were inhibited by tebuconazole. Nitrification rate was also inhibited but only during the first 30 days. Different functional community profiles were observed depending on the tebuconazole concentration used. It was concluded that tebuconazole application decreases soil microbial biomass and activity.     

Immediate and adaptational temperature effects on nitric oxide production and nitrous oxide release from nitrification and denitrification in two soils

 Nitrification and denitrification are, like all biological processes, influenced by temperature. We investigated temperature effects on N trace gas turnover by nitrification and denitrification in two soils under two experimental conditions. In the first approach ("temperature shift experiment") soil samples were preincubated at 25  °C and then exposed to gradually increasing temperatures (starting at 4  °C and finishing at 40–45  °C). Under these conditions the immediate effect of temperature change was assessed. In the second approach ("discrete temperature experiment") the soil samples were preincubated at different temperatures (4–35  °C) for 5 days and then tested at the same temperatures. The different experimental conditions affected the results of the study. In the temperature shift experiment the NO release increased steadily with increasing temperature in both soils. In the discrete temperature experiment, however, the production rates of NO and N₂O showed a minimum at intermediate temperatures (13–25  °C). In one of the soils (soil B9), the percent contribution of nitrification to NO production in the discrete temperature experiment reached a maximum (>95% contribution) at 25  °C. In the temperature shift experiment nitrification was always the dominant process for NO release and showed no systematic temperature dependency. In the second soil (soil B14), the percent contribution of nitrification to NO release decreased from 50 to 10% as the temperature was increased from 4  °C to 45  °C, but no differences were evident in the discrete temperature experiment. The N₂O production rates were measured in the discrete temperature experiment only. The contribution of nitrification to N₂O production in soil B9 was considerably higher at 25–35  °C (60–80% contribution) than at 4–13  °C (15–20% contribution). In soil B14 the contribution of nitrification to N₂O production was lowest at 4  °C. The effects of temperature on N trace gas turnover differed between the two soils and incubation conditions. The experimental set-up allowed us to distinguish between immediate effects of short-term changes in temperature on the process rates, and longer-term effects by which preincubation at a particular temperature presumably resulted in the adaptation of the soil microorganisms to this temperature. Both types of effects were important in regulating the release of NO and N₂O from soil. Received: 20 October 1998     

Does history matter? Temperature effects on soil microbial biomass and community structure based on the phospholipid fatty acid (PLFA) analysis

Background, aim, and scope

Temperature is an important environmental factor regulating soil microbial biomass, activity, and community. Soils from different climatic regions may have very different dominant soil microbes, which are acclimated to the local conditions like temperature. Changing soil temperature especially warming has been shown to increase the mortality rate of soil microbes. However, little is known about the responses of soil microbes coming from different climatic regions to different incubation temperatures. The objective of this study was to examine the temperature effects on microbial biomass and community of soils collected from cold, intermediate, and hot natural sites.

Materials and methods

Soils were collected from northern (Heilongjiang province), central (Jiangsu province), and southern (Guangxi province) China, these soils having very different temperature histories. The Heilongjiang soil was from the coldest region with a mean annual temperature of 1.2°C, the Jiangsu soil was intermediate with a mean annual temperature of 15.7°C, and Guangxi soil was from the hottest area, with a mean annual temperature of 21.2°C. These three soils were incubated at 4°C, 15°C, 25°C, and 35°C for up to 56 days. Phospholipid fatty acid (PLFA) analyses were conducted on days 0, 3, 7, 14, 28, and 56 to track the dynamics of soil microbes.

Results

Soil microbial biomass indexed by total phospholipid fatty acid concentration decreased with increasing incubation temperature, with that of the Heilongjiang soil decreasing most. At the end of incubation, the biomass at 35°C in the Heilongjiang, Jiangsu, and Guangxi soils had declined to 65%, 72%, and 96% of the initial biomass, respectively. The PLFA patterns shifted with increasing temperatures in all the soils, especially at 35°C; the change was biggest in the Heilongjiang soil.

Discussion

History does have effects on soil microbes responding to environmental stress. Soil microbial biomass and PLFA profiles shifted least in the Guangxi soil with the hottest temperature history and most in the Heilongjiang soil with the coldest temperature, indicating that the distribution of free-living microorganisms is influenced by climatic factors. The majority of soil microorganisms coming from the hot regions are more adapted to high temperature (35°C) compared to those from the cold area. There are some regular changes of PLFA profiles when increasing incubation temperature to 35°C. However, the effect of incubation temperature on soil microbial community structure was inconclusive. As PLFA profile community structure is the phenotypic community structure. Genotype experiments are required to be done in future studies for the better understanding of soil microbes in different climate regions with concerning temperature variation.

Conclusions

With the increasing incubation temperature, soil microbial biomass and PLFA profiles shifted most in the soil with the coldest temperature history and least in the soil with the hottest temperature. History does matter in determining soil microbial dynamics when facing thermal stress.     

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     

Scots pine (Pinus sylvestris L.) roots and soil moisture did not affect soil thermal sensitivity

Through their effects on microbial metabolism, temperature and moisture affect the rate of decomposition of soil organic matter. Plant roots play an important role in SOM mineralization and nutrient cycling. There are reports that rhizosphere soil exhibits higher sensitivity to temperature than root-free soil, and this can have implications for how soil CO₂ efflux may be affected in a warmer world. We tested the effects of 1-week incubation under different combinations of temperature (5, 15, 30 ^°C) and moisture (15, 50, 100% WHC) on the respiration rate of soil planted with Scots pine and of unplanted soil. Soil respiration in both soils was the highest at moderate moisture (p < 0.0001) and, increased with temperature (p < 0.0001). There was also marginally significant effect of soil kind on respiration rate (p < 0.055), but the significant interaction of temperature effect with soil kind effect, indicated, that soil respiration of planted soil was higher than unplanted soil only at 5 ^°C (p < 0.05). The soil kind effect was compared also as Q₁₀ coefficients for respiration rate, showing the relative change in microbial activity with increased temperature. However, there was no difference in the thermal sensitivity of soil respiration between planted and unplanted soils (p = 0.99), irrespective of the level of soil moisture. These findings were similar to the latest studies and confirmed, that in various models, being useful tools in studying of soil carbon cycling, there is no need to distinguish between planted and unplanted soil as different soil carbon pools.