Effects of land-use and management practices on soil ergosterol content in andosols

Ergosterol is a fungus-specific chemical component which has been extensively used to assess the fungal biomass and activity in soils. In the present study, we investigated the soil ergosterol content in a group of Japanese soils differing in management. In addition, the relationships among the soil ergosterol content (SEC), microbial biomass C (MBC), and microbial biomass N (MBN) were also tested in different seasons. Our results showed that the SEC was lower in intensively cropped soils than in pasture and forest soils. In general, no consistent trend was observed for SEC of pasture soils within the same sampling period. However, SEC tended to decrease in most of the soils in autumn, which may be ascribed to the effect of seasonal changes on fungal biomass. No strong evidence could be obtained for the effect of different fertilizers on SEC, which can be due to different management variables and interspecific variations between fungal communities at different soil sites. Our results did not suggest the presence of a noticeable correlation between SEC and MBC or MBN. The ratio of SEC in total biomass C was lower (0.20 and 0.11% in spring and autumn, respectively) compared with the values reported.     

LONG‐TERM LAND USE INFLUENCES SOIL MICROBIAL BIOMASS P AND S,PHOSPHATASE AND ARYLSULFATASE ACTIVITIES,AND S MINERALIZATION IN A BRAZILIAN OXISOL

Land use choices differentially affect soil physical and biological properties. Tillage choices in particular affect soil erosion, the retention of soil organic matter, and the biological activity that organic matter supports. The present study evaluated the consequences of different cropping and tillage systems (undisturbed forest, coffee plantation, conventional, and no‐tillage row cropping) for soil microbial indicators and sulfur mineralization after 24 years of cropping on an Oxisol (Typic Haplorthox) in an experimental area at Londrina, Brazil. Soil samples were taken at 0–5, 5–10, and 10–20 cm depths and evaluated for microbial biomass P and S, S mineralization, and phosphatase and arylsulfatase activities. Land use affected microbial biomass P and S, and enzyme activity at all depths studied. The cultivated sites had lower values of microbial activity than the undisturbed forested site. Although the coffee site was not tilled and had high organic carbon content, there was low microbial activity, probably due to higher soil acidity and Al content. The estimates of pool stock for microbial P and annual P flux through the soil microbial biomass suggest that these pools are large enough to significantly affect plant nutrient availability. The greater microbial biomass and activity under forested and no‐tillage sites may be attributed, at least partially, to higher organic matter content. The soil microbial variables examined proved to be strong indicators of soil sustainability. Copyright © 2013 John Wiley & Sons, Ltd.     

Long‐term effects of leguminous cover crops on microbial indices and their relationships in soils of a coconut plantation of a humid tropical region

In this study, leguminous crops like Atylosia scarabaeoides, Centrosema pubescens, Calopogonium mucunoides, and Pueraria phaseoloides. grown as soil cover individually in the interspaces of a 19‐yr‐old coconut plantation in S. Andaman (India) were assessed for their influence on various microbial indices (microbial biomass C, biomass N, basal respiration, ergosterol, levels of ATP, AMP, ADP) in soils (0–50 cm) collected from these plots after 10 years. The effects of these cover crops on . CO₂ (metabolic quotient), adenylate energy charge (AEC), and the ratios of various soil microbial properties viz., biomass C : soil organic C, biomass C : N, biomass N : total N, ergosterol : biomass C, and ATP : biomass C were also examined. Cover cropping markedly enhanced the levels of organic matter and microbial activity in soils after the 10‐yr‐period. Microbial biomass C and N, basal respiration, . CO₂, ergosterol and levels of ATP, AMP, ADP in the cover‐cropped plots significantly exceeded the corresponding values in the control plot. While the biomass C : N ratio tended to decrease, the ratios of biomass N : total N, ergosterol : biomass C, and ATP : biomass C increased significantly due to cover cropping. Greater ergosterol : biomass C ratio in the cover‐cropped plots indicated a decomposition pathway dominated by fungi, and high . CO₂ levels in these plots indicated a decrease in substrate use efficiency probably due to the dominance of fungi. The AEC levels ranged from 0.80 to 0.83 in the cover‐cropped plots, thereby reflecting greater microbial proliferation and activity. The ratios of various microbial and chemical properties could be assigned to three different factors by principal components analysis. The first factor (PC1) with strong loadings of ATP : biomass C ratio, AEC, and . CO₂ reflected the specific metabolic activity of soil microbes. The ratios of ergosterol : biomass C, soil organic C : total N, and biomass N : total N formed the second factor (PC2) indicating a decomposition pathway dominated by fungi. The biomass C : N and biomass C : soil organic C ratios formed the third principal component (PC3), reflecting soil organic matter availability in relation to nutrient availability. Overall, the study suggested that Pueraria phaseoloides. or Atylosia scarabaeoides were better suited as cover crops for the humid tropics due to their positive contribution to soil organic C, N, and microbial activity.     

The effects of N and P additions on soil microbial properties in paired stands of temperate secondary forests and adjacent larch plantations in Northeast China

The conversion of secondary forests to larch plantations in Northeast China has resulted in a significant decline in soil available nitrogen (N) and phosphorus (P), and thus affects plant productivity and ecosystem functioning. Microbes play a key role in the recycling of soil nutrients; in turn, the availability of soil N and P can constrain microbial activity. However, there is little information on the relationships between available soil N and P and the microbial biomass and activity in larch plantation soil. We studied the responses of soil microbial respiration, microbial biomass and activity to N and P additions in a 120-day laboratory incubation experiment and assessed soil microbial properties in larch plantation soil by comparing them with the soil of an adjacent secondary forest. We found that the N-containing treatments (N and N + P) increased the concentrations of soil microbial biomass N and soluble organic N, whereas the same treatments did not affect microbial respiration and the activities of β-glucosidase, N-acetyl-β-glucosaminidase and acid phosphatase in the larch plantation. In addition, the concentration of microbial biomass P decreased with N addition in larch plantation soil. In contrast, N and N + P additions decreased microbial respiration, and N addition also decreased the activity of N-acetyl-β-glucosaminidase in the secondary forest soil. The P treatment did not affect microbial respiration in either larch plantation or secondary forest soils, while this treatment increased the activities of β-glucosidase and acid phosphatase in the secondary forest soil. These results suggested that microbial respiration was not limited by available P in either secondary forest or larch plantation soils, but microbial activity may have a greater P demand in secondary forest soil than in larch plantation soil. Overall, there was no evidence, at least in the present experiment, supporting the possibility that microbes suffered from N or P deficiency in larch plantation soil.     

Ergosterol and microbial biomass relationship in soil

Ergosterol and microbial biomass C were measured in 26 arable, 16 grassland and 30 forest soils. The ergosterol content ranged from 0.75 to 12.94 g g^-1 soil. The geometric mean ergosterol content of grassland and forest soils was around 5.5 g g^-1, that of the arable soils 2.14 g g^-1. The ergosterol was significantly correlated with biomass C in the entire group of soils, but not in the subgroups of grassland and forest soils. The geometric mean of the ergosterol: microbial biomass C ratio was 6.0 mg g^-1, increasing in the order grassland (5.1), arable land (5.4) and woodland (7.2). The ergosterol:microbial biomass C ratio had a strong negative relationship with the decreasing cation exchange capacity and soil pH, indicating that the fungal part of the total microbial biomass in soils increased when the buffer capacity decreased. The average ergosterol concentration calculated from literature data was 5.1 mg g^-1 fungal dry weight. Assuming that fungi contain 46% C, the conversion factor from micrograms ergosterol to micrograms fungal biomass C is 90. For soil samples, neither saponification of the extract nor the more effective direct saponification during extraction seems to be really necessary.     

Soil Fertility,Mineral Nitrogen,and Microbial Biomass in Upland Soils of the Central Amazon under Different Plant Covers

Amazon is the largest state in Brazil and majority of the state is covered by the largest tropical rainforest of the world. Most soils of the Amazon region soils are acidic and infertile. When the Amazon forest land is cleared for agricultural use by burning the vegetation, the efficient nutrient recycling mechanisms are disrupted. However, nutrient contents in the deforested burn land increased temporarily. The objective of this study was to evaluate the soil fertility, mineral nitrogen (N), and microbial activity of carbon (C), N, and phosphorus (P) resulting from the replacement of the primary forest with pasture (Brachiaria brizantha) and commercial plantations of rubber (Hevea spp.), cupuaçu (Theobroma grandiflorum), and citrus trees (Citrus sinensis) cultivated in Xanthic Ferralsol and secondary forest under Acrisols Dystric Nitosols. The results showed that ammonium-N predominates in the 0- to 10-cm soil depth in both primary forest and areas with secondary forest, citrus plantation, and pasture. There was no increase in soil fertility with management of the cultivated areas under the secondary forest, but in the pasture there was a significant increase in the stock of organic C and total N and high C/N ratios, the inverse of what occurred with the C of the microbial biomass. The primary forest had the greatest values of C and P of the microbial biomass and the lowest metabolic quotient. Of the successions studied, the rubber trees were the plant cover with the smallest changes in terms of quality of the organic matter in the soil.     

Soil biochemical and microbial indices in wet tropical forests: Effects of deforestation and cultivation

Little information is available about the long‐term effects of deforestation and cultivation on biochemical and microbial properties in wet tropical forest soils. In this study, we evaluated the general and specific biochemical properties of soils under evergreen, semi‐evergreen, and moist deciduous forests and adjacent plantations of coconut, arecanut, and rubber, established by clear felling portions of these forests. We also examined the effects of change in land use on microbial indices and their interrelationships in soils. Significant differences between the sites occurred for the biochemical properties reflecting soil microbial activity. Microbial biomass C, biomass N, soil respiration, N mineralization capacity, ergosterol, levels of adenylates (ATP, AMP, ADP), and activities of dehydrogenase and catalase were, in general, significantly higher under the forests than under the plantations. Likewise, the activities of various hydrolytic enzymes such as acid phosphomonoesterase, phosphodiesterase, casein‐protease, BAA‐protease, β‐glucosidase, CM‐cellulase, invertase, urease, and arylsulfatase were significantly higher in the forest soils which suggested that deforestation and cultivation markedly reduced microbial activity, enzyme synthesis and accumulation due to decreased C turnover and nutrient availability. While the ratios of microbial biomass C : N and microbial biomass C : organic C did not vary significantly between the sites, the ratios of ergosterol : biomass C and ATP : biomass C, qCO2 and AEC (Adenylate Energy Charge) levels were significantly higher in the forest sites indicating high energy requirements of soil microbes at these sites.     

Soil microbial biomass, activity and community composition in adjacent native and plantation forests of subtropical Australia

Purpose

Soil nitrogen (N) availability is a critical determinant of plantation productivity in subtropical Australia and is influenced by the soil microbial community. The size, structure and function of the soil microbial community can be impacted by land-use change and residue management. The objectives of this study were to examine the impact of land-use change from (1) native forest (NF) to first rotation (1R) hoop pine plantation and (2) 1R hoop pine plantation to second rotation (2R) hoop pine plantation on the soil microbial community. The impact of residue management on the soil microbial community was also investigated in the 2R forest, where soil microbial parameters were measured in tree rows (2R-T) and windrows (2R-W). In addition, relationships between soil microbial parameters and soil N parameters were investigated.

Materials and methods

Each of the four treatments (NF, 1R, 2R-T and 2R-W) had five 24-m² replicate plots from which 15 soil cores were collected and bulked at three depths (0–10, 10–20, 20–30 cm). Microbial biomass carbon (MBC) and N (MBN) and soil respiration were measured on field moist soils. In addition, carbon (C) source utilisation patterns were assessed using the whole soil MicroResp? technique (Campbell et al. 2003).

Results and discussion

Results indicate that the land-use change from NF to 1R hoop pine plantation significantly reduced MBC, respiration rate, soil total C and total N. Furthermore, the land-use change appeared to have a significant impact on the soil microbial community composition measured using MicroResp? profiles. Land-use change from 1R to 2R hoop pine plantation resulted in a decline in total C and MBN and a shift in microbial community composition. When compared to the 2R-T soils, the 2R-W soils tended to have a greater microbial biomass and respiration rate. Residue management also influenced the microbial community composition measured in the MicroResp? profiles.

Conclusions

Results indicate that land-use change had a significant impact on the soil microbial community, which was likely to be related to shifts in the quality and quantity of organic inputs associated with the change in land use. This may have significant implications for the long-term productivity of the soil resource. Further studies are required to confirm a difference in microbial community composition associated with residue management. In addition, long-term experiments in subtropical Australia are necessary to verify the results of this snapshot study and to improve our understanding of the impact of single-species plantation forestry and residue management on the soil microbial community, soil N dynamics and ultimately the long-term sustainability of the soil resource.     

Soil microbial activity and biomass is stimulated by leguminous cover crops

The leguminous cover crops Atylosia scarabaeoides (L.) Benth., Centrosema pubescens Benth., and Pueraria phaseoloides (Roxb.) Benth., were grown in the interspaces of a 19 y–old coconut plantation and incorporated into the soil at the end of the monsoon season every year. At the end of the 12th year, soils from different depths were collected and analyzed for various microbial indices and their interrelationships. The objectives were to assess the effects of long‐term cover cropping on microbial biomass and microbial‐community structure successively down the soil profile. In general, total N (TN), organic C (OC), inorganic N, extractable P, and the levels of biological substrates viz., dissolved organic C (DOC) and N (DON), labile organic N (LON), and light‐fraction organic matter (LFOM) C and N decreased with depth at all the sites. Among sites, the cover‐cropped (CC) sites possessed significantly greater levels of TN, OC, DOC, DON, and LON compared to the control. Consequently, microbial biomass C (MBC), N (MBN), and P (MBP), CO₂ evolution, and ATP levels, in general, decreased with depth at all sites and were also significantly higher in the CC sites. Among the ratios of various microbial indices, the ratio of MBC to OC and metabolic quotient (qCO₂) declined with depth. Higher MBC‐to‐OC ratios and large qCO₂ levels in the surface soils could be ascribed to greater levels of readily degradable C content and indicated short turnover times of the microbial biomass. In contrast, the ratios of MBC to MBN and MBC to MBP increased with depth due to low N/P availability and relatively higher C availability in the subsoils. Cover cropping tended to enhance the ratios of MBC to OC, MBC to MBN, MBC to MBP, and ergosterol to MBC and decreased the ATP‐to‐MBC ratio at all depths. The relatively lower ATP‐to‐MBC ratios in the CC site, especially in the subsoil indicated microbial‐community structure possibly dominated by fungi. By converting the ergosterol content to fungal biomass, it was observed that fungi constituted 52%–63% of total biomass C at the CC site, but only 33%–40% of total biomass C at the control site. Overall, the study indicated that leguminous cover crops like P. phaseoloides or A. scarabaeoides significantly enhanced the levels of OC, N and microbial activity in the soils, even down to 50 cm soil depth.     

Microbial biomass and activities in partly hydromorphic agricultural and forest soils in the Bornhöved Lake region of Northern Germany

The soil microbial biomass and activity were estimated for seven field (intensive and extensive management), grassland (dry and wet), and forest (beech, dry and wet alder) sites. Three of the sites (wet grassland, dry and wet alder) are located on a lakeshore and are influenced by lake water and groundwater. Four different methods were selected to measure and characterize the microbial biomass. Values of microbial biomass (weight basis) and total microbial biomass per upper horizon and hectare (volume basis) were compared for each site.Fumigation-extraction and substrate-induced respiration results were correlated but dit not give the same absolute values for microbial biomass content. When using the original conversion factors, substrate-induced respiration gave higher values in field and dry grassland soils, and fumigation-extraction higher values in soils with low pH and high water levels (high organic content). Results from dimethylsulfoxide reduction and arginine ammonification, two methods for estimating microbial activity, were not correlated with microbial biomass values determined by fumigation-extraction or substrate-induced respiration in all soils examined. In alder forest soils dimethylsulfoxide reduction and arginine ammonification gave higher values on the wet site than on the dry site, contrary to the values estimated by fumigation-extraction and substrate-induced respiration. These microbial activities were correlated with microbial biomass values only in field and dry grassland soils. Based on soil dry weight, microbial biomass values increased in the order intensive field, beech forest, extensive field, dry grassland, alder forest, wet grassland. However, microbial biomass values per upper horizon and hectare (related to soil volume) increased in agricultural soils in the order intensive field, dry grassland, extensive field, wet grassland and in forest soils in the order beech, wet alder, dry alder. We conclude that use of the original conversion factors with the soils in the present study for fumigation-extraction and substrate-induced respiration measurements does not give the same values for the microbial biomass. Furthermore, dimethylsulfoxide reduction and arginine ammonification principally characterize specific microbial activities and can be correlated with microbial biomass values under specific soil conditions. Further improvements in microbial biomass estimates, particularly in waterlogged soils, may be obtained by direct counts of organisms, ATP estimate, and the use of ¹⁴C-labelled organic substrates. From the ecological viewpoint, data should also be expressed per horizon and hectare (related to soil volume) to assist in the comparison of different sites.     

Coffee mucilage impact on young coffee seedlings and soil microorganisms

A greenhouse pot experiment was carried out to assess the effects of fermented coffee mucilage applied as mulch together with maize leaves on the growth of young coffee plants of two different varieties and on soil microbial biomass indices. The coffee variety Catuai required 32% more water per g plant biomass than the variety Yellow Caturra, but had a 49% lower leaf area, 34% less shoot and 46% less root biomass. Maize and mucilage amendments did not affect leaf area, shoot and root yield, or the N concentration in shoot and root dry matter. The amendments always reduced the water use efficiency values, but this reduction was only significant in the maize+mucilage‐14 (= 14 g mucilage pot^?1) treatment. Soil pH significantly increased from 4.30 in the control to 4.63 in the maize+mucilage‐14 treatment. Microbial biomass C increased by 18.5 µg g^?1 soil, microbial biomass N by 3.1 µg g^?1 soil, and ergosterol by 0.21 µg g^?1 soil per g mucilage added pot^?1. The presence of mucilage significantly reduced the microbial biomass‐C/N ratio from a mean of 13.4 in the control and maize treatments to 9.3, without addition rate and coffee variety effects. The application of non‐composted mucilage is recommended in areas where drought leads to economic losses and in coffee plantations on low fertility soils like Oxisols, where Al toxicity is a major constraint.     

Land-use history,forest conversion,and soil organic carbon in pine plantations and native forests of south eastern Australia

Land-use history – the number, type, and duration of previous land uses – is relevant to many questions regarding land-use effects on soil carbon, but is infrequently reported. We examine the importance of land-use history variables, as well as topographic and edaphic variables, on soil C in a range of forest types – native forest, pine plantations, secondary forest and rehabilitated forest – at three contrasting locations in south eastern Australia. Our comparisons include a novel forest conversion of exotic pine plantations to native, broadleaf forest.Using nested ANOVAs, we detected few differences in soil C concentration indices (total C, microbial biomass C, K₂SO₄–C) and C content among eucalypt-dominated vegetation and pine plantations within each location (0–10 cm depth). However, planned contrasts indicated a 30% decrease in soil C content with conversion of native forest to pine plantation of age 37 years. The reverse land-use change – pine plantation to native, broadleaf forest – was associated with a decrease in soil C concentration and content at one location (40%; age 12–13 years) and no detectable changes at another (to age 7 years). Variable effect between locations of this novel land-use change on soil C could be due to differences in potential productivity, conifer species, and plantation age.We used correlation coefficients and general linear models to identify widely applicable variables for predicting soil C concentration and content at local scales (≤ 20 km²). Within-location relationships with topographic variables were weak and infrequent relative to those with edaphic and land-use history variables. Soil texture was strongly correlated with soil C at each location, although the relative significance of different particle size fractions differed among locations. Electrical conductivity appeared more widely applicable since it was included in C models at two locations. Combining land-use history and edaphic variables produced strong predictive models for soil C concentrations and content at two locations (total r² 0.83 to 0.95). Positive relationships were indicated between soil C and ‘age of current vegetation’ at one location, and negative relationships were indicated with ‘number of land uses’ at another. These data highlight a potential predictive role for land-use history variables in local-scale assessments of soil C in forested landscapes.     

Impact of deforestation on soil physicochemical characteristics,microbial biomass and microbial activity of tropical soil

The study dealt with the assessment of the impact of deforestation on tropical soil through a comparative analysis of physicochemical and microbiological parameters of natural forest and a deforested barren site. With significant decline in clay, texturally the soil of the deforested barren site was observed to be different from that of natural forest. Bulk density and porosity data revealed structural deterioration of deforested barren soil. The soil hydrological regime was also adversely affected by the deforestation. Levels of soil organic carbon, total nitrogen, microbial biomass C, N and microfungal biomass also exhibited significant decline in deforested site. Analysis of microbial respiratory quotient (q CO₂) was also observed to be impaired in the deforested site. Copyright © 2001 John Wiley & Sons, Ltd.     

Multivariate approach to characterizing soil microbial communities in pristine and agricultural sites in Northwest Argentina

Land use effects on microbial communities may have profound impacts on agricultural productivity and ecosystem sustainability as they are critical in soil quality and health. The main aim of this study was to characterize the microbial communities of pristine and agricultural soils in the central Yungas region in Northwest Argentina. As a first step in the development of biological indicators of soil quality in this region, a comprehensive approach involving a structural and functional evaluation of microbial communities was used to detect changes in soil as consequence of land use. The sites selected included two pristine montane forest sites (MF1 and MF2), two plots under sugarcane monoculture for 40 and 100 years (SC40 and SC100), one plot under 20 years of soybean monoculture (SB20), a recently deforested and soybean cropped site (RC), and two reference sites of native forest adjacent to the sugarcane and soybean plots (PF1 and PF2). We used three microbial community profiling methods: denaturing gradient gel electrophoresis (DGGE) analysis of PCR amplified 16S rRNA genes, community-level physiological profiling (CLPP) using a BD oxygen biosensor system (BDOBS-CLPP) and phospholipid fatty acid (PLFA) analysis. Deforestation and agriculture caused expected increases in pH and decreases in organic carbon and microbial biomass. Additionally, shifts in the microbial community structure and physiology were detected with disturbance, including reduced diversity based on PLFA data. The higher respiratory response to several carbon substrates observed in agricultural soils suggested the presence of microbial communities with lower growth yield efficiency that could further reduce carbon storage in these soils.Using an integrated multivariate analysis of all data measured in this study we propose a minimum data set of variables (organic carbon, pH, sucrose and valeric acid utilizations, a17:0 and a15:0 PLFA biomarkers and the value of impact on microbial diversity) to be used for future studies of soil quality in Northwest Argentina.     

Influence of leguminous cover crops on microbial and selected enzyme activities in soils of a plantation

A study dealing with ecological sustainability of plantation based land use initiated in 1991 in a 19 yr old coconut plantation consists of growing certain leguminous crops like Atylosia, Pueraria, Centrosema and Calopogonium as soil cover in separate plots with lemon grass as live bounds. These cover crops are grown during the rainy season and incorporated into the soil towards the end of the monsoon every year. The effect of such cover crops on soil microbial counts (total counts, fungi, actinomycetes and bacteria), biomass C, organic C, total N and on the activity of enzymes like urease, amidase, L-glutaminase, aryl sulphatase and dehydrogenase was determined in soils (Ap horizon) collected from these plots after 5 years. Soils with cover crops registered significantly higher microbial biomass, biomass C, organic C and total N compared to control. Consequently, all the enzymes were activated to different degrees in soils with cover crops. Significant and positive relationships of enzyme activities with organic C, mineral N and total N suggested that growing cover crops, increased C turnover and N availability and therefore, provided a conducive environment for microbial proliferation, enzyme synthesis and accumulation in the soil matrix.     

Land-use intensification and agroforestry in the Kenyan highland: Impacts on soil microbial community composition and functional capacity

This study investigates microbial communities in soil from sites under different land use in Kenya. We sampled natural forest, forest plantations, agricultural fields of agroforestry farms, agricultural fields with traditional farming and eroded soil on the slopes of Mount Elgon, Kenya. We hypothesised that microbial decomposition capacity, biomass and diversity (1) decreases with intensified cultivation; and (2) can be restored by soil and land management in agroforestry. Functional capacity of soil microbial communities was estimated by degradation of 31 substrates on Biolog EcoPlates™. Microbial community composition and biomass were characterised by phospholipid fatty acid (PLFA) and microbial C and N analyses. All 31 substrates were metabolised in all studied soil types, i.e. functional diversity did not differ. However, both the substrate utilisation rates and the microbial biomass decreased with intensification of land use, and the biomass was positively correlated with organic matter content. Multivariate analysis of PLFA and Biolog EcoPlate™ data showed clear differences between land uses, also indicated by different relative abundance of PLFA markers for certain microorganism groups. In conclusion, our results show that vegetation and land use control the substrate utilisation capacity and microbial community composition and that functional capacity of depleted soils can be restored by active soil management, e.g. forest plantation. However, although 20–30 years of agroforestry farming practises did result in improved soil microbiological and chemical conditions of agricultural soil as compared to traditional agricultural fields, the change was not statistically significant.     

Microbial communities of a native perennial bunchgrass do not respond consistently across a gradient of land-use intensification

To test if native perennial bunchgrasses cultivate the same microbial community composition across a gradient in land-use intensification, soils were sampled in fall, winter and spring in areas under bunchgrasses (‘plant’) and in bare soils (‘removal’) in which plots were cleared of living plants adjacent to native perennial bunchgrasses (Nassella pulchra). The gradient in land-use intensification was represented by a relict perennial grassland, a restored perennial grassland, and a perennial grass agriculture site on the same soil type. An exotic annual grassland site was also included because perennial bunchgrasses often exist within a matrix of annual grasses in California. Differences in soil resource pools between ‘plant’ and ‘removal’ soils were observed mainly in the relict perennial grassland and perennial grass agriculture site. Seasonal responses occurred in all sites. Microbial biomass carbon (C) and dissolved organic C were greater under perennial bunchgrasses in the relict perennial grassland and perennial grass agriculture site when comparing treatment means of ‘plant’ vs. ‘removal’ soil. In general, soil moisture, microbial respiration, and nitrate decreased from fall to spring in ‘plant’ and ‘removal’ soils, while soil ammonium and net mineralizable nitrogen (N) increased only in ‘plant’ soils. A canonical correspondence analysis (CCA) of phospholipid fatty acid (PLFA) profiles from all sites showed that land-use history limits the similarity of microbial community composition as do soil C and N dynamics among sites. When PLFA profiles from individual sites were analyzed by CCA, different microbial PLFA markers were associated with N. pulchra in each site, indicating that the same plant species does not retain a unique microbial fingerprint across the gradient of land-use intensification.     

Stoichiometric responses of soil microflora to nutrient additions for two temperate forest soils

The ratios of soil carbon (C) to nitrogen (N) and C to phosphorus (P) are much higher in Chinese temperate forest soils than in other forest soils, implying that N and P might limit microbial growth and activities. The objective of this study was to assess stoichiometric responses of microbial biomass, enzyme activities, and respiration to N and P additions. We conducted a nutrient (N, P, and N + P) addition experiment in two temperate soils under Korean pine (Pinus koraiensis) plantation and natural broadleaf forest in Northeast China and measured the microbial biomass C, N, P; the activities of β-glucosidase (BG), N-acetyl-β-glucosaminidase (NAG), and acid and alkaline phosphomonoesterase (AP); and the microbial respiration in the two soils. Nitrogen addition increased microbial biomass N and decreased microbial biomass C-to-N ratio and microbial respiration in the two soils. Nitrogen addition decreased NAG activity to microbial biomass N ratio, P addition decreased AP activity to microbial biomass P ratio, and N, P, and N + P additions all increased BG activity to microbial biomass C ratio. These results suggest that microbial stoichiometry is not strictly homeostatic in response to nutrient additions, especially for N addition. The responses of enzyme activities to nutrient additions support the resource allocation theory. The N addition induced a decline in microbial respiration, implying that atmospheric N deposition may reduce microbial respiration, and consequently increase soil C sequestration in the temperate region.     

Fungal presence in paired cultivated and uncultivated soils in central Iowa, USA

 Amounts of fungal biomass in adjacent cultivated and uncultivated soils in central Iowa were estimated and compared by quantifying soil ergosterol concentrations and lengths of fungal hyphae present. Both indices of fungal biomass, with one exception, indicated that there was at least twice as much fungal biomass in uncultivated soil as in cultivated soil. Levels of microbial biomass carbon in uncultivated soils were also determined to be at least twice that in cultivated soils. Data collected in this study indicate that fungi may be more significantly affected by agricultural soil management practices than other components of the soil microbial community. For two of the soils examined, calculated estimates denote that fungal biomass carbon represented approximately 20% of the total microbial biomass carbon in cultivated soil and about 33% of the microbial biomass carbon in uncultivated soil. Results of this study indicate that conventional agricultural practices result in a significant reduction of fungal biomass production in soil. Implications of differences in fungal biomass between the soils are discussed. Received: 12 October 1997     

Does biochar interfere with standard methods for determining soil microbial biomass and phenotypic community structure?

Due to its high sorption affinity for organic compounds, biochar may interfere with extraction procedures involving such compounds used for microbially-related assays commonly applied to soils. Here we assessed the impact of two biochars (derived from pine bark and produced at 300 and 600 °C) at three concentrations (0, 12.5, and 50 g kg⁻¹) in three distinct arable soils with contrasting textural classes (loamy sand, sandy loam, and clay) on the determination of soil microbial biomass C by fumigation–extraction, fungal biomass by ergosterol analysis, and microbial community structure as defined by phospholipid fatty acid (PLFA) profiling. Biochar did not affect the apparent concentration of soil microbial biomass C and had no significant impact on apparent PLFA profiles. By contrast, the apparent extraction efficiency of ergosterol was affected dependent on soil type, biochar production temperature, and biochar concentration. Nonetheless, ergosterol contents of biochar-amended soils can be accurately estimated by correcting for reduced recovery using an ergosterol spike.