scholarly journals Perennial herbaceous legumes as live soil mulches and their effects on C, N and P of the microbial biomass

2003 ◽  
Vol 60 (1) ◽  
pp. 139-147 ◽  
Author(s):  
Gustavo Pereira Duda ◽  
José Guilherme Marinho Guerra ◽  
Marcela Teixeira Monteiro ◽  
Helvécio De-Polli ◽  
Marcelo Grandi Teixeira

The use of living mulch with legumes is increasing but the impact of this management technique on the soil microbial pool is not well known. In this work, the effect of different live mulches was evaluated in relation to the C, N and P pools of the microbial biomass, in a Typic Alfisol of Seropédica, RJ, Brazil. The field experiment was divided in two parts: the first, consisted of treatments set in a 2 x 2 x 4 factorial combination of the following factors: live mulch species (Arachis pintoi and Macroptilium atropurpureum), vegetation management after cutting (leaving residue as a mulch or residue remotion from the plots) and four soil depths. The second part had treatments set in a 4 x 2 x 2 factorial combination of the following factors: absence of live mulch, A. pintoi, Pueraria phaseoloides, and M. atropurpureum, P levels (0 and 88 kg ha-1) and vegetation management after cutting. Variation of microbial C was not observed in relation to soil depth. However, the amount of microbial P and N, water soluble C, available C, and mineralizable C decreased with soil depth. Among the tested legumes, Arachis pintoi promoted an increase of microbial C and available C content of the soil, when compared to the other legume species (Pueraria phaseoloides and Macroptilium atropurpureum). Keeping the shoot as a mulch promoted an increase on soil content of microbial C and N, total organic C and N, and organic C fractions, indicating the importance of this practice to improve soil fertility.

2017 ◽  
Vol 14 (8) ◽  
pp. 2155-2166 ◽  
Author(s):  
Ruzhen Wang ◽  
Linyou Lü ◽  
Courtney A. Creamer ◽  
Feike A. Dijkstra ◽  
Heyong Liu ◽  
...  

Abstract. Soil coarseness decreases ecosystem productivity, ecosystem carbon (C) and nitrogen (N) stocks, and soil nutrient contents in sandy grasslands subjected to desertification. To gain insight into changes in soil C and N pools, microbial biomass, and enzyme activities in response to soil coarseness, a field experiment was conducted by mixing native soil with river sand in different mass proportions: 0, 10, 30, 50, and 70 % sand addition. Four years after establishing plots and 2 years after transplanting, soil organic C and total N concentrations decreased with increased soil coarseness down to 32.2 and 53.7 % of concentrations in control plots, respectively. Soil microbial biomass C (MBC) and N (MBN) declined with soil coarseness down to 44.1 and 51.9 %, respectively, while microbial biomass phosphorus (MBP) increased by as much as 73.9 %. Soil coarseness significantly decreased the enzyme activities of β-glucosidase, N-acetyl-glucosaminidase, and acid phosphomonoesterase by 20.2–57.5 %, 24.5–53.0 %, and 22.2–88.7 %, used for C, N and P cycling, respectively. However, observed values of soil organic C, dissolved organic C, total dissolved N, available P, MBC, MBN, and MBP were often significantly higher than would be predicted from dilution effects caused by the sand addition. Soil coarseness enhanced microbial C and N limitation relative to P, as indicated by the ratios of β-glucosidase and N-acetyl-glucosaminidase to acid phosphomonoesterase (and MBC : MBP and MBN : MBP ratios). Enhanced microbial recycling of P might alleviate plant P limitation in nutrient-poor grassland ecosystems that are affected by soil coarseness. Soil coarseness is a critical parameter affecting soil C and N storage and increases in soil coarseness can enhance microbial C and N limitation relative to P, potentially posing a threat to plant productivity in sandy grasslands suffering from desertification.


Soil Research ◽  
1992 ◽  
Vol 30 (4) ◽  
pp. 493 ◽  
Author(s):  
MR Carter ◽  
PM Mele

Changes and relationships for organic C, microbial biomass C and N, and soil structural stability indices were determined at the soil surface after 10 years of direct drilling stubble retained (DDR) and stubble burnt (DDB), and cultivation with stubble burnt (CCB) for cropping systems on a sandy clay loam, duplex soil (calcic luvisol) in south-eastern Australia. Direct drilling caused a slight but significant increase in soil organic C at the 0-25 mm soil depth compared to the cultivated treatment. Microbial biomass C and N increases over the 0-100 mm soil depths were seasonal and generally greater for the DDR in comparison with DDB and CCB systems. Use of short duration wet sieving for the 0-25 mm soil depth showed a significant increase in aggregate stability for the DDR, especially for 2-10 mm sized aggregates, compared with the other tillage treatments. Such differences were reduced by standard wet sieving or use of a dispersion test illustrating the fragile nature of these unstable aggregates developed under cropping systems. Soil structural indices (water stable aggregates >2.00 mm, and >0.25 mm; mean weight diameter) were weakly correlated with increases in microbial biomass (r = 0.45, P < 0.01) and to total organic C (r = 0.35, P < 0.05). For these tillage systems, microbial biomass tended to be a poor predictor of changes in soil organic C. Overall, the long term effect of direct drilling and stubble retention in these cropping systems provided only relatively minor increases in organic C and, consequently, aggregate stability.


2020 ◽  
Author(s):  
Laurent K. Kidinda ◽  
Folasade K. Olagoke ◽  
Cordula Vogel ◽  
Karsten Kalbitz ◽  
Sebastian Doetterl

Abstract. Microbial processes are one of the key factors driving carbon (C) and nutrient cycling in terrestrial ecosystems, and are strongly driven by the equilibrium between resource availability and demand. In deeply weathered tropical rainforest soils of Africa, it remains unclear whether patterns of microbial processes differ between soils developed from geochemically contrasting parent materials. Here we show that resource availability across soil depths and regions from mafic to felsic geochemistry shape patterns of soil microbial processes. During a 120-day incubation experiment, we found that microbial biomass C and extracellular enzyme activity were highest in the mafic region. Microbial C limitation was highest in the mixed sedimentary region and lowest in the felsic region, which we propose is related to the strength of contrasting C stabilization mechanisms and varying C quality. None of the investigated regions and soil depths showed signs of nitrogen (N) limitation for microbial processes. Microbial phosphorus (P) limitation increased with soil depth but was similar across geochemical regions, indicating that subsoils in the investigated soils were depleted in rock-derived nutrients and are therefore dependent on efficient biological recycling of nutrients. Microbial C limitation was lowest in subsoils, indicating that subsoil microbes can significantly participate in C cycling and limit C storage if increased oxygen availability is prevalent. Using multivariable regressions, we demonstrate that microbial biomass C normalized to soil organic C content (MBCSOC) is controlled by soil geochemistry and substrate quality, while microbial biomass C normalized to soil weight (MBCSoil) is predominantly driven by resource distribution. We conclude that due to differences in resource availability, microbial processes in deeply weathered tropical rainforest soils greatly vary across geochemical regions which must be considered when assessing soil microbial processes in organic matter turnover models.


1996 ◽  
Vol 76 (4) ◽  
pp. 459-467 ◽  
Author(s):  
William R. Horwath ◽  
Eldor A. Paul ◽  
David Harris ◽  
Jeannette Norton ◽  
Leslie Jagger ◽  
...  

Chloroform fumigation-incubation (CFI) has made possible the extensive characterization of soil microbial biomass carbon (C) (MBC). Defining the non-microbial C mineralized in soils following fumigation remains the major limitation of CFI. The mineralization of non-microbial C during CFI was examined by adding 14C-maize to soil before incubation. The decomposition of the 14C-maize during a 10-d incubation after fumigation was 22.5% that in non-fumigated control soils. Re-inoculation of the fumigated soil raised 14C-maize decomposition to 77% that of the unfumigated control. A method was developed which varies the proportion of mineralized C from the unfumigated soil (UFC) that is subtracted in calculating CFI biomasss C. The proportion subtracted (P) varies according to a linear function of the ratio of C mineralized in the fumigated (FC) and unfumigated samples (FC/UFC) with two parameters K1 and K2 (P = K1FC/UFC) + K2). These parameters were estimated by regression of CFI biomass C, calculated according to the equation MBC = (FC − PUFC)/0.41, against that derived by direct microscopy in a series of California soils. Parameter values which gave the best estimate of microscopic biomass from the fumigation data were K1 = 0.29 and K2 = 0.23 (R2 = 0.87). Substituting these parameter values, the equation can be simplified to MBC = 1.73FC − 0.56UFC. The equation was applied to other CFI data to determine its effect on the measurement of MBC. The use of this approach corrected data that were previously difficult to interpret and helped to reveal temporal trends and changes in MBC associated with soil depth. Key words: Chloroform fumigation-incubation, soil microbial biomass, microscopically estimated biomass, carbon, control, 14C


2011 ◽  
Vol 51 (No. 6) ◽  
pp. 276-282 ◽  
Author(s):  
T. Šimon

The content of aliphatic compounds, hydrophobicity index, organic C and N content and the microbial biomass and respiration activity were analysed in soil samples originating from different plots of a long-term field experiment (variants: nil, NPK &ndash; mineral fertilization: 64.6&ndash;100 kg/ha/year, FYM &ndash; farmyard manure and FYM + NPK) from three blocks (III, IV and B) with different crop rotation. Samples were taken from 0&ndash;200 mm layer in 2002 and 2003 (spring and autumn). The plots without any fertilization had the significantly lowest aliphatic compound content compared to variants fertilized by FYM or FYM + NPK in all the evaluated blocks in both years. The variants fertilized only by mineral NPK without any organic fertilization had the slightly increased aliphatic compound content but they did not exceed significantly the control variants in most cases. The aliphatic compound contents correlated significantly with the organic C contents in 2002 and 2003, as well. The values of the hydrophobicity index showed a similar trend like the data mentioned above. Organic manure increased the soil organic nitrogen content, similarly to the carbon content. In variants fertilized by FYM and FYM + NPK the higher microbial biomass content was found comparing to unfertilized variants. Correlations between aliphatic compound content and biomass differed in spring (2002: r = 0.065, 2003: r = 0.068) and autumn (2002: r = 0.407, 2003: r = 0.529). Organically fertilized variants had increased basal respiration, in autumn 2002 the basal respiration was higher in variants fertilized by mineral NPK, too. The highest specific respiration was recorded in the unfertilised plot in block B (autumn 2002 and 2003), where low microbial biomass exhibited high activity. Increased specific respiration was found also in plots fertilized by FYM and FYM&nbsp;+ NPK (block III and IV, autumn samplings). Positive significant correlations between microbial biomass content and basal respiration were found in 2002 (spring: r = 0.716) and 2003 (spring: r = 0.765, autumn: r = 0.671).


1999 ◽  
Vol 79 (1) ◽  
pp. 73-84 ◽  
Author(s):  
C. A. Campbell ◽  
V. O. Biederbeck ◽  
G. Wen ◽  
R. P. Zentner ◽  
J. Schoenau ◽  
...  

Measurements of seasonal changes in soil biochemical attributes can provide valuable information on how crop management and weather variables influence soil quality. We sampled soil from the 0- to 7.5-cm depth of two long-term crop rotations [continuous wheat (Cont W) and both phases of fallow-wheat (F–W)] at Swift Current, Saskatchewan, from early May to mid-October, 11 times in 1995 and 9 times in 1996. The soil is a silt loam, Orthic Brown Chernozem with pH 6.0, in dilute CaCl2. We monitored changes in organic C (OC) and total N (TN), microbial biomass C (MBC), light fraction C and N (LFC and LFN), mineralizable C (Cmin) and N (Nmin), and water-soluble organic C (WSOC). All biochemical attributes, except MBC, showed higher values for Cont W than for F–W, reflecting the historically higher crop residue inputs, less frequent tillage, and drier conditions of Cont W. Based on the seasonal mean values for 1996, we concluded that, after 29 yr, F–W has degraded soil organic C and total N by about 15% compared to Cont W. In the same period it has degraded the labile attributes, except MBC, much more. For example, WSOC is degraded by 22%, Cmin and Nmin by 45% and LFC and LFN by 60–75%. Organic C and TN were constant during the season because one year's C and N inputs are small compared to the total soil C or N. All the labile attributes varied markedly throughout the seasons. We explained most of the seasonal variability in soil biochemical attributes in terms of C and N inputs from crop residues and rhizodeposition, and the influences of soil moisture, precipitation and temperature. Using multiple regression, we related the biochemical attributes to soil moisture and the weather variables, accounting for 20% of the variability in MBC, 27% of that of Nmin, 29% for LFC, 52% for Cmin, and 66% for WSOC. In all cases the biochemical attributes were negatively related to precipitation, soil moisture, temperature and their interactions. We interpreted this to mean that conditions favouring decomposition of organic matter in situ result in decreases in these attributes when they are measured subsequently under laboratory conditions. We concluded that when assessing changes in OC or TN over years, measurements can be made at any time during a year. However, if assessing changes in the labile soil attributes, several measurements should be made during a season or, measurements be made near the same time each year. Key words: Microbial biomass, carbon, nitrogen, mineralization, water-soluble-C, light fraction, weather variables


2002 ◽  
Vol 68 (8) ◽  
pp. 3859-3866 ◽  
Author(s):  
W. Shi ◽  
J. Becker ◽  
M. Bischoff ◽  
R. F. Turco ◽  
A. E. Konopka

ABSTRACT Microbial community composition and activity were characterized in soil contaminated with lead (Pb), chromium (Cr), and hydrocarbons. Contaminant levels were very heterogeneous and ranged from 50 to 16,700 mg of total petroleum hydrocarbons (TPH) kg of soil−1, 3 to 3,300 mg of total Cr kg of soil−1, and 1 to 17,100 mg of Pb kg of soil−1. Microbial community compositions were estimated from the patterns of phospholipid fatty acids (PLFA); these were considerably different among the 14 soil samples. Statistical analyses suggested that the variation in PLFA was more correlated with soil hydrocarbons than with the levels of Cr and Pb. The metal sensitivity of the microbial community was determined by extracting bacteria from soil and measuring [3H]leucine incorporation as a function of metal concentration. Six soil samples collected in the spring of 1999 had IC50 values (the heavy metal concentrations giving 50% reduction of microbial activity) of approximately 2.5 mM for CrO4 2− and 0.01 mM for Pb2+. Much higher levels of Pb were required to inhibit [14C]glucose mineralization directly in soils. In microcosm experiments with these samples, microbial biomass and the ratio of microbial biomass to soil organic C were not correlated with the concentrations of hydrocarbons and heavy metals. However, microbial C respiration in samples with a higher level of hydrocarbons differed from the other soils no matter whether complex organic C (alfalfa) was added or not. The ratios of microbial C respiration to microbial biomass differed significantly among the soil samples (P < 0.05) and were relatively high in soils contaminated with hydrocarbons or heavy metals. Our results suggest that the soil microbial community was predominantly affected by hydrocarbons.


Soil Research ◽  
2007 ◽  
Vol 45 (1) ◽  
pp. 13 ◽  
Author(s):  
Fiona A. Robertson ◽  
Peter J. Thorburn

The Australian sugar industry is moving away from the practice of burning the crop before harvest to a system of green cane trash blanketing (GCTB). Since the residues that would have been lost in the fire are returned to the soil, nutrients and organic matter may be accumulating under trash blanketing. There is a need to know if this is the case, to better manage fertiliser inputs and maintain soil fertility. The objective of this work was to determine whether conversion from a burning to a GCTB trash management system is likely to affect soil fertility in terms of C and N. Indicators of short- and long-term soil C and N cycling were measured in 5 field experiments in contrasting climatic conditions. The effects of GCTB varied among experiments. Experiments that had been running for 1–2 years (Harwood) showed no significant trash management effects. In experiments that had been running for 3–6 years (Mackay and Tully), soil organic C and total N were up to 21% greater under trash blanketing than under burning, to 0.10 or 0.25 m depth (most of this effect being in the top 50 mm). Soil microbial activity (CO2 production) and soil microbial biomass also increased under GCTB, presumably as a consequence of the improved C availability. Most of the trash C was respired by the microbial biomass and lost from the system as CO2. The stimulation of microbial activity in these relatively short-term GCTB systems was not accompanied by increased net mineralisation of soil N, probably because of the greatly increased net immobilisation of N. It was calculated that, with standard fertiliser applications, the entire trash blanket could be decomposed without compromising the supply of N to the crop. Calculations of possible long-term effects of converting from a burnt to a GCTB production system suggested that, at the sites studied, soil organic C could increase by 8–15%, total soil N could increase by 9–24%, and inorganic soil N could increase by 37 kg/ha.year, and that it would take 20–30 years for the soils to approach this new equilibrium. The results suggest that fertiliser N application should not be reduced in the first 6 years after adoption of GCTB, but small reductions may be possible in the longer term (>15 years).


SOIL ◽  
2021 ◽  
Vol 7 (1) ◽  
pp. 95-106
Author(s):  
Jennifer M. Rhymes ◽  
Irene Cordero ◽  
Mathilde Chomel ◽  
Jocelyn M. Lavallee ◽  
Angela L. Straathof ◽  
...  

Abstract. It is widely accepted that the measurement of organic and inorganic forms of carbon (C) and nitrogen (N) in soils should be performed on fresh extracts taken from fresh soil samples. However, this is often not possible, and it is common practice to store samples (soils and/or extracts), despite a lack of guidance on best practice. We utilised a case study on a temperate grassland soil taken from different depths to demonstrate how differences in soil and/or soil extract storage temperature (4 or −20 ∘C) and duration can influence sample integrity for the quantification of soil-dissolved organic C and N (DOC and DON), extractable inorganic nitrogen (NH4+ and NO3-) and microbial biomass C and N (MBC and MBN). The appropriateness of different storage treatments varied between topsoils and subsoils, highlighting the need to consider appropriate storage methods based on soil depth and soil properties. In general, we found that storing soils and extracts by freezing at −20 ∘C was least effective at maintaining measured values of fresh material, whilst refrigerating (4 ∘C) soils for less than a week for DOC and DON and up to a year for MBC and MBN and refrigerating soil extracts for less than a week for NH4+ and NO3- did not jeopardise sample integrity. We discuss and provide the appropriate tools to ensure researchers consider best storage practice methods when designing and organising ecological research involving assessments of soil properties related to C and N cycling. We encourage researchers to use standardised methods where possible and to report their storage treatment (i.e. temperature, duration) when publishing findings on aspects of soil and ecosystem functioning. In the absence of published storage recommendations for a given soil type, we encourage researchers to conduct a pilot study and publish their findings.


Sign in / Sign up

Export Citation Format

Share Document