C:N:P stoichiometry and nutrient limitation of the soil microbial biomass in a grazed grassland site under experimental P limitation or excess
© Griffiths et al.; licensee Springer. 2012
Received: 16 April 2012
Accepted: 19 May 2012
Published: 21 June 2012
The availability of essential nutrients, such as nitrogen (N) and phosphorus (P), can feedback on soil carbon (C) and the soil microbial biomass. Natural cycles can be supplemented by agricultural fertiliser addition, and we determined whether the stoichiometry and nutrient limitation of the microbial biomass could be affected by an unbalanced nutrient supply.
Samples were taken from a long-term trial (in effect since 1968) with annual applications of 0, 15 and 30 kg P ha−1 with constant N and potassium. Soil and microbial biomass CNP contents were measured and nutrient limitation assessed by substrate-induced respiration. Linear regression and discriminant analyses were used to identify the variables explaining nutrient limitation.
Soil and biomass CNP increased with increasing P fertiliser, and there was a significant, positive, correlation between microbial biomass P and biomass C, apart from at the highest level of P fertilisation when the microbial biomass was over-saturated with P. The molar ratios of C:N:P in the microbial biomass remained constant (homeostatic) despite large changes in the soil nutrient ratios. Microbial growth was generally limited by C and N, except in soil with no added P when C and P were the main limiting nutrients. C, N and P, however, did not explain all the growth limitation on the soils with no added P.
Increased soil C and N were probably due to increased net primary production. Our results confirm that C:N:P ratios within the microbial biomass were constrained (i.e. homeostatic) under near optimum soil conditions. Soils with no added P were characterised by strong microbial P limitation and soils under high P by over-saturation of microorganisms with P. Relative changes in biomass C:P can be indicative of nutrient limitation within a site.
KeywordsCarbon Nitrogen Nutrient limitation Phosphorus Soil microbial biomass Stoichiometry
In terrestrial ecosystems most primary production enters the decomposer pathway (Cebrian1999), where microorganisms mineralise organic material to simple inorganic compounds and recycle growth-limiting nutrients for autotrophs. This is essential for soil fertility and plant growth. Microorganisms require the nutrients for their own growth and generally the carbon-to-nutrient ratio determines whether nutrients are immobilised in the microbial biomass or mineralised to become available for uptake. The soil microbial biomass therefore acts as both a sink and a source of nutrients which become available during the turnover of microbial biomass. The availability and limitation of essential nutrients, such as nitrogen (N) and phosphorus (P), can thus feed back on soil carbon (C) dynamics and microbial biomass (Wang et al.2010; Brookes2001).
In a global-scale meta-analysis of the C:N:P ratio of soil and the soil microbial biomass (Cleveland and Liptzin2007), the abundance and ratio of elements were constrained. While this was not surprising for C and N, given that plants are the major source of both C and N in the soil, relatively fixed C:P and N:P ratios were more unexpected given that organisms do not regulate the total amount of soil P. The amount of P available for plant uptake is related to the total soil P and so indirectly links the abundance of P with that of C and N in soil (Cleveland and Liptzin2007). Thus, microbial C:N:P ratios are strongly related and not significantly affected by variations in soil element ratios. This has given rise to the suggestion that differences in soil microbial biomass element ratios could provide an insight into nutrient limitation in terrestrial ecosystems (Cleveland and Liptzin2007). In managed systems nutrient addition is commonly practised, and even in unmanaged systems nutrient deposition occurs, so the objective of this study was to determine how soil and soil microbial biomass elemental ratios responded to nutrient addition.
In agricultural systems the natural biogeochemical cycles can be supplemented by the addition of readily available, inorganic fertilisers. Agricultural productivity in Ireland has historically been limited by P, but the application of fertiliser P, which peaked in the 1970s, has resulted in an increase in levels of available soil P such that about 50% of Irish grassland soils no longer respond to added P (Culleton et al.2002). Overall fertiliser consumption in Ireland is now falling, from 430,000, 62,000 and 151,000 tonnes N, P, K respectively (N:P 6.9) in 1994 to the latest available figures of 307,000, 20,000 and 52,000 tonnes (N:P 15.2) in 2008 (DAFF2008). In 2002 Irish grasslands received an average of 123, 11 and 27 kg N, P, K ha−1 year−1 (N:P 11.2) (Coulter et al.2004). Even so, the majority of P in typical grassland soil is present as organic P which represents a large pool of potentially available nutrient (Bourke et al. 2008). Although the agronomic objective of the added nutrients is to increase plant production, they will also be available to the soil microbial biomass. The soil microorganisms will see an indirect increase in soil C, from increased rhizodeposition and increased residue incorporation from the extra plant growth, and a direct increase in N and P from the added nutrients. Microorganisms can compete effectively with plants for these nutrients (Schimel et al.1989; Zak et al.1990). Applied inorganic N, for example, is rapidly taken up by the soil microbial biomass (Nannipieri et al.1990) which can be limited by nutrients and not just C (Kaye and Hart1997; Wang and Bakken1997), although the outcome of the plant–microorganism competition depends on the spatial heterogeneity of the system (Korsaeth et al.2001). Previous work on cut, rather than grazed, grassland showed clearly that both microbial biomass P and the biomass C:P ratio were sensitive to long-term (>100 years) fertiliser regimes (He et al.1997). Growth experiments using environmental isolates of bacteria recently demonstrated that their stoichiometry is very flexible, with a four-fold change in C:P ratio between P-sufficient and P-deficient conditions (Scott et al.2012). This could result in a less homeostatic variation in C:N:P ratios within a site than suggested by the meta-analysis of (Cleveland and Liptzin2007).
Given the changing inputs of inorganic nutrients to many grassland soils, we felt it timely to determine whether the stoichiometry of the soil microbial biomass could be affected by an unbalanced nutrient supply and if we could experimentally show nutrient limitation of the soil microbial biomass. To do this we sampled plots from a long-term agricultural trial instigated in 1968 (Culleton et al.2002). Phosphorus had been applied annually at 0, 15 and 30 kg ha−1, with the plots split in 1999 to reduce P applications to half the high-P plots and increase P to half the low-P plots (as detailed below). Soil microbial biomass and its elemental CNP composition were measured and total soil C, N and P determined. In addition, respiration measurements were conducted to assess nutrient constraints at different fertilisation levels. This would test if differences in soil microbial biomass element ratios in an agricultural situation could provide an insight into nutrient limitation in terrestrial ecosystems (Cleveland and Liptzin2007), or whether microbial biomass element ratios may be responsive to altered fertiliser regimes (Scott et al.2012).
Cowlands long-term, grazed field trial
The plots were sampled in April 2009. Two separate composite soil samples were collected from the top 10 cm of each plot by taking 20 cores for each composite sample with a gouge auger (1.25 cm diameter) in a stratified random design. The soils were handpicked to remove stones and larger soil fauna, sieved to pass through a 3.35 mm mesh and incubated for 6 days at 25°C to allow respiration to settle down after sieving without letting the soils dry out. Water-holding capacity of each treatment was determined and sub-samples of each plot were oven-dried for 24 h at 105°C for dry weight (d.w.) analysis.
Soil C, N, P
Total C and N in samples were determined using an elemental analyser (Thermo Scientific Flash EA 2000). Total P was extracted in aqua regia (ISO 11466: 1995) and measured by ICP.
Soil microbial biomass C, N, P
Microbial biomass C, N and P were measured by the chloroform fumigation-extraction (CFE) technique (Brookes et al.1984,1985; Vance et al.1987): 10 g d.w. equivalent of soil was fumigated for 24 h at 25°C and extracted with 0.5 M K2SO4 (for C and N) or 0.5 M NaHCO3 (for P). C, N and P from unfumigated soils were extracted in the same way. In the extracts we determined the following: total organic carbon (TOC) by combustion (Baird2005) using a Shimadzu TOC-VCPH analyser with ASI-V autosampler; total organic nitrogen (TON) by alkaline persulfate oxidation (Cabrera and Beare1993); inorganic phosphorus (Pi) by the ammonium molybdate-ascorbic acid method (Watanabe and Olsen1965). Soil microbial biomass element content was calculated as the difference between the fumigated and unfumigated samples using conversion factors of 0.45 for C (Wu et al.1990), 0.45 for N (Jenkinson et al.2004) and 0.40 for P (Hedley and Stewart1982).
Microbial nutrient limitation
Microbial parameters were determined by a substrate-induced respiration method (Anderson and Domsch1978) using an automated respirometer based on electrolytic O2 microcompensation (Scheu1992). The oxygen consumption rates of 3 g d.w. soil samples were measured at 22°C.
For basal respiration (μl O2 g−1 h−1), the average oxygen consumption was measured 15–20 h after attachment of samples to the respirometer. For SIR measurements, glucose was added to the soil samples in a concentration of 8,000 ppm C, sufficient to induce maximum respiration. The mean of the three lowest measurements during the first 10 h after glucose addition was taken as maximum initial respiratory response (MIRR). Microbial biomass C (Cmic, μg g−1) was calculated as 38 × MIRR (Beck et al.1997). The specific respiration (q O2, μl O2 mg−1 Cmic h−1) was calculated using data on microbial biomass and basal respiration.
In order to detect nutrient limitation of the soil microbial biomass, combinations of nutrients were added in excess (Scheu1993). Carbon (8,000 ppm glucose), nitrogen ((NH4)2SO4) and phosphorus (K2HPO4) were added in combination to individual soil samples in a C:N:P ratio of 10:2:1, corresponding to the average element composition of microorganisms in soil. The slope of the microbial growth curves representing microbial growth ability in C, CN, CP and CNP amended samples was taken as a measure of microbial nutrient limitation.
Statistical analyses were performed in ‘R’, version 2.12.2. For stoichiometric analysis data were converted into molar ratios. Data were tested for normal distribution of residuals and homogeneity of variance. Outliers were substituted by mean values, and data were log-transformed if necessary. A one-factorial analysis of variance with the factors ‘P-fertilisation treatment’ and ‘water content’ as co-variables was conducted. If significant, post-hoc tests using Tukey’s test at P < 0.05 tested for differences between means. The results are presented as arithmetic means. Linear regression analysis was conducted and the coefficients of determination (r2) were calculated for soil C and N content, microbial biomass C and P, and log-log plot of total or available soil C:P ratio versus microbial biomass C:P ratio. Discriminant analysis with Tree Classifiers was used to select explanatory variables in multiple regression analysis. Using Akaike’s Information Criterion the minimum adequate model in multiple regression analysis was calculated according to Crawley (2007).
Results and Discussion
Soil C, N, P
Soil and microbial biomass chemistry
Soil C (g)
Soil N (g)
Soil P (mg)
Biomass C_CFE (mg)
Biomass C_SIR (mg)
Biomass N (μg)
Biomass P (μg)
Molar C:N:P ratios in soil and microbial biomass
Total soil pools
Soil microbial biomass C, N, P
Biomass C was least in 0_0 and greatest in 30_0, whether determined by CFE or SIR (Table1). In general soil microbial biomass C, N and P accumulated with increasing fertiliser P (Table1). P treatment did not significantly affect the biomass C:N ratio, which ranged from 5.9 to 7.1 (Table2), but molar element ratios involving P were significantly affected, with the C:P ratio being significantly greater in 0_0 (C:P 16.7) than any other treatment (e.g. C:P 30_30, 10.8) (Table1), and while the N:P ratio was greatest in 0_0 (2.3), it was only significantly greater than the 0_30 and 30_30 (1.6) treatments (Table2).
Dissolved organic C and N (i.e. extracted from unfumigated soil during the determination of microbial biomass) behaved differently from P (Table1). Extractable C and N were significantly greater in the 0_0 treatment and less but stable with added P, whereas extractable P was least in the 0_0 treatment and increased with increasing P.
Microbial nutrient limitation
Regression model results for microbial nutrient limitation
C:Psoil × Cmic:DOC
N:Pmic × Cmic:DOC
CNlmt × N:Pmic × C:Nmic
Clmt × N:Psoil
N:Pmic × Clmt
N:Pmic × N:Psoil
The Cowlands long-term phosphorus trial
Previous measurements showed that the 15_15 plots were the most productive, having significantly greater live weight gain from the grazed cattle than the 0_0, while the 30_30 plots had a similar live weight gain to the 15_15 but significantly more P loss from overland flow (Culleton et al.2002). The treatments in the Cowlands long-term field trial were changed in 1999 because the high stocking rate was found to be more productive across all P treatments (Culleton et al.2002). The comparison then shifted to determining how quickly productivity in the 0_30 plots could be restored, how long accumulated soil P could sustain production in the 30_0 plots and whether reduced application rates in the 15_5 plots were sufficient to maintain optimum productivity (King-Salter2008). The vegetation composition of the four high P treatments (15_15, 15_5, 30_30, 30_0) was essentially the same, dominated by Lolium perenne and Poa trivialis, whereas the 0_0 plots were botanically different and dominated by Agrostis capillaris and Holcus lanatus (King-Salter2008). The 0_30 plots were intermediate, botanically, and were returning to a high-P-type sward. The treatments, therefore, show a range in P availability, being deficient enough in the 0_0 plots to affect botanical composition, plant productivity and live weight gain, and in surplus enough in the 30_30 plots for excess P to be lost by overland flow. It should be noted that even where levels of inorganic P (Pi) were low enough to affect botanical composition (0_0) there were still considerable amounts of organic P (Po) present in the soil, 460 μg Po g−1, but clearly not available for plant uptake (King-Salter2008).
Phosphorus is relatively immobile in soil and tends to accumulate (Brookes2001), which would explain the observation that P-fertilisation led to a strong linear increase (2.25-fold) for soil P from unfertilised to medium and high fertilised (0_0 < 15_15 < 30_30) grasslands. Long-term P-application led to increasing soil C and N contents, probably due to increased net primary production of the vegetation and a subsequent positive feed back by detritus to the soil organic matter (Bever et al.1997).
The values of Pi extracted from the unfumigated samples were higher than measured in some studies (e.g. 2, 6 and 17 μg Pi g−1 for 0_0, 15_15 and 30_30 respectively measured by Culleton et al. (2002) and Fu (2009)), but lower than measured by King-Salter (2008) (e.g. 55, 235 and 435 μg Pi g−1) for the same plots. The differences can be attributed to the different extractants used, as the acetate-acetic acid extraction (Morgan P) used by (Culleton et al.2002, Fu2009and King-Salter2008) is known to give a lower value for Pi than the bicarbonate extraction (Olsen P) used in this study (Foy et al.1997), while King-Salter (2008) extracted with dilute sulphuric acid. The concentration of Pi in the unfumigated extracts gave the same trend as microbial biomass P and total soil P (i.e. a linear increase as total P application increased), except for the 30_30 treatment. Thus, a total of 900 kg P ha−1 had been applied to the 30_0 plots up to 2009 and 1,200 kg P ha−1 to the 30_30 plots (an increase of 1.4-fold), similarly Pmic increased by 1.1-fold and total soil P by 1.2-fold but extractable Pi almost doubled with a 1.8-fold increase. This indicates over-saturation of P as discussed below.
Nutrient limitation of the microbial biomass
We used the CFE technique to determine soil microbial biomass element ratios which, while commonly used, does have limitations which may lead to errors in microbial C, N and P estimation (as discussed by Jenkinson et al. (2004), Cleveland and Liptzin (2007)).
The Cowlands trial was grazed, so that even in the no-P fertiliser plots there would have been some return and recycling of organic matter to the sward. All the data indicate that the microorganisms in 0_0 are P limited: the soil microbial biomass had significantly greater C:P than the other treatments. The respiratory quotient indicated a greater degree of stress; microbial response to added nutrients was significantly inhibited and was significantly relieved by the addition of P. The fact that in the respiration experiments with added CNP the 0_0 soil did not respire at the same rate as the other soils implies that this soil is still suffering from limitation by another nutrient, but compared to the effects of adding extra P this is minor. This limitation was removed by the addition of P fertiliser in the 0_30 treatment, which showed no such P limitation 10 years after fertiliser had started to be applied. The opposite effect was less evident in the 30_0 soil from which P fertiliser had been removed for the last 10 years, although there was an indication that the microbial parameters were moving towards signs of P limitation (an increase in C:P ratio and reduced responses to added nutrients compared to the 30_30 soil). In this sense the soil microbial biomass mirrored the response of the vegetation (King-Salter2008).
In a comparison of forest types in China, Liu et al. (2012) showed that soil respiration measured in situ was significantly enhanced by P fertilisation in an old-growth forest, which was by nature of N-saturation necessarily P-limited, whereas less P-deficient disturbed forests showed no or a lesser respiratory response to P fertilisation.
Microbial community structure
Measuring the gross changes in microbial biomass nutrient contents in response to P fertilisation overlooks any changes in microbial community structure which might explain some of the observed changes. It is likely that the species composition of the microbial biomass would differ in 0_0 from the other treatments due to the change in CNP stoichiometry. Since fungal biomass contains relatively more C than bacterial biomass, it is suggested that fungi might have a higher C-demand than bacteria, while bacteria are more constrained by nutrient ratios (Keiblinger et al.2010). We found only a weak correlation between the CFE and SIR measurements of Cmic, and variation was particularly large in the high P-fertiliser treatments (15_15, 30_0, 30_30). According to Beck et al. (1997) the difference between the two methods is largest when soils contain a disproportionately large component of microorganisms using glucose as an energy source, suggesting a shift in microbial community structure in the high-P soils. The respiratory quotient measurements also indicated a change to the microbial community in the 0_0 soil, with an increase (i.e. more respiration per unit biomass) being indicative of stressed cells or a change in microbial community structure (Anderson and Domsch1990), although the respiratory quotient showed no variation with reducing P input from the highest level, 30_30 to 30_0. This is supported by measurements at the Cowlands site which indicate an altered microbial community structure (as measured by phospho-lipid fatty acid (PLFA) analysis and nematode community analysis) and decreasing fungal-to-bacterial ratio as P fertilisation increases (Chen, unpublished data). Liu et al. (2012) similarly showed an altered PLFA pattern in the P-limited old-growth forest with added P, but in their case an increased fungal-to-bacterial ratio. Phosphate has recently been shown to be an important driver of microbial community structure in a range of soils (Kuramae et al.2012).
Response of C:N:P to P fertilisation
The size and elemental composition of the soil microbial biomass in the Cowlands was within the range reported from other temperate grasslands, with biomass C contents of 150–2,800 μg C g−1 and biomass P contents of 40–170 μg P g−1 with C:P ratios of 11–76 (Brookes et al.1984; He et al.1997). However under extreme fertilisation regimes, such as N-only fertiliser since 1897 in a hay meadow (i.e. limited return of organic matter from the cut sward), microbial biomass P can fall to below 10 μg P g−1 and the C:P ratio rise to 276 (He et al.1997). Under managed conditions, therefore, the stoichiometry of the soil microbial biomass can be significantly affected and fall outside the normal range.
The overall soil C:N:P ratio calculated by Cleveland and Liptzin (2007) for grassland soils (166:12:1) is very close to that of our high P 30_30 treatment (156:13:1) but quite far from that of our 0_0 treatment (302:25:1) suggesting that their study might have been based on P-rich soils. The data used by Cleveland and Liptzin partly originated from a study by Turner et al. (2001), who measured soil microbial biomass C, N and P in 29 UK permanent grassland soils by CFE as well as by a UV absorbance procedure. Their soil P contents (0.094 ± 0.032%) were as high as that in our 30_30 treatment (0.091 ± 0.005%). Our microbial C:N ratios were very constant among all treatments supporting the hypothesis of a well constrained ratio within the microbial biomass. Constant C:P ratios occurred predominantly in the medium treatments, but this could be due to a shift in microbial community structure. Our results confirm that C:N:P ratios within the microbial biomass were constrained (homeostatic) as long as soil conditions were not far away from the optimum.
Long-term P-application led to increasing soil and microbial C, N and P contents, with C and N probably reflecting increased net primary production. There were also indications of an altered microbial community structure. Our results confirm that C:N:P ratios within the microbial biomass were constrained (homeostatic) under near optimum soil conditions. Thus, molar nutrient ratios in the soil averaged 219:18:1 and in the microbial biomass the average was 36:5:1. Soils with no added P were characterised by strong microbial nutrient limitation (P and minor nutrients) and soils under high P by over-saturation of microorganisms with P. Relative changes in soil microbial biomass C:P can be indicative of nutrient limitation within a site.
BSG is supported by Science Foundation Ireland grant no. 07/SK/B1236b.
- Anderson JPE, Domsch KH: A physiological method for the quantitative measurement of microbial biomass in soils. Soil Biol Biochem 1978, 10: 215–221. 10.1016/0038-0717(78)90099-8View ArticleGoogle Scholar
- Anderson T-H, Domsch KH: Application of eco-physiological quotients ( q CO 2 and q D) on microbial biomasses from soils of different cropping histories. Soil Biol Biochem 1990, 22: 251–255. 10.1016/0038-0717(90)90094-GView ArticleGoogle Scholar
- Baird RB: Aggregate organic constituents; total organic carbon (TOC)/method 5310 B High temperature combustion method. In Standard methods for the examination of waters and waste water. 21st edition. Edited by: Eaton DA, Clesceri LS, Rice EW, Greensberg AE. American Public Health Association, Washington DC; 2005.Google Scholar
- Beck T, Joergensen RG, Kandeler E, Makeschin F, Nuss E, Oberholzer HR, Scheu S: An inter-laboratory comparison of ten different ways of measuring soil microbial biomass C. Soil Biol Biochem 1997, 29: 1023–1032. 10.1016/S0038-0717(97)00030-8View ArticleGoogle Scholar
- Bever J, Westover K, Antonovics J: Incorporating the soil community into plant population dynamics: the utility of the feedback approach. J Ecol 1997, 85: 561–573. 10.2307/2960528View ArticleGoogle Scholar
- Brookes PC: Minireview. The soil microbial biomass: concept, measurement and applications in soil ecosystem research. Microbes Environ 2001, 16: 131–140. 10.1264/jsme2.2001.131View ArticleGoogle Scholar
- Bourke D, Dowding P, Tunney H, O’Brien JE, Jeffrey DW: The organic phosphorus composition of an Irish grassland soil. Biol Environ 2008, 108B: 17–28.Google Scholar
- Brookes PC, Powlson DS, Jenkinson DS: Phosphorus in the soil microbial biomass. Soil Biol Biochem 1984, 16: 169–175. 10.1016/0038-0717(84)90108-1View ArticleGoogle Scholar
- Brookes PC, Landman A, Pruden G, Jenkinson DS: Chloroform fumigation and the release of soil-nitrogen—a rapid direct extraction method to measure microbial biomass nitrogen in soil. Soil Biol Biochem 1985, 17: 837–842. 10.1016/0038-0717(85)90144-0View ArticleGoogle Scholar
- Cabrera ML, Beare MH: Alkaline persulfate oxidation for determining total nitrogen in microbial biomass extracts. Soil Sci Soc Am J 1993, 57: 1007–1012. 10.2136/sssaj1993.03615995005700040021xView ArticleGoogle Scholar
- Cebrian J: Patterns in the fate of production in plant communities. Am Nat 1999, 15: 449–468.View ArticleGoogle Scholar
- Cleveland CC, Liptzin D: C:N:P stoichiometry in soil: is there a "Redfield ratio" for the microbial biomass? Biogeochemistry 2007, 85: 235–252. 10.1007/s10533-007-9132-0View ArticleGoogle Scholar
- Coulter BS, Murphy WE, Culleton N, Quinlan G: A survey of fertilizer use in Ireland for 2001 and 2002 and some comparisons with Teagasc nutrient advice. Fert Assoc Ireland Proc 2004, 41: 24.Google Scholar
- Crawley M: Statistics - An introduction using R. Wiley, Chichester; 2007. 950 pp 950 ppGoogle Scholar
- Culleton N, Coulter B, Liebhardt WC: The fate of phosphatic fertiliser applied to grassland. Ir Geogr 2002, 35: 175–184. 10.1080/00750770209555803View ArticleGoogle Scholar
- DAFF: Fertiliser consumption, 1989/2005—2007/2008. 2008. . Accessed 23 Feb 2012 http://www.agriculture.gov.ie/media/migration/publications/2008/compendium2008/individual/H5.xls . Accessed 23 Feb 2012Google Scholar
- Elser JJ, Dobberfuhl DR, MacKay NA, Scampel JH: Organisms size, life history, and N:P stoichiometry. Bioscience 1996, 46: 674–684. 10.2307/1312897View ArticleGoogle Scholar
- Foy RH, Tunney H, Carroll MJ, Byrne E, Gately T, Bailey JS, Lennox SD: A comparison of Olsen and Morgan soil phosphorus test results from the cross-border region of Ireland. Irish J Agr Food Res 1997, 36: 185–193.Google Scholar
- Fu W: Spatial variation of extractable phosphorus and other nutrients in Irish grassland soils. PhD Thesis, NUI Galway, Galway, Ireland; 2009.Google Scholar
- Hall EK, Maixner F, Franklin O, Daims S, Richter A, Battin T: Linking microbial and ecosystem ecology using ecological stoichiometry: a synthesis of conceptual and empirical approaches. Ecosystems 2010. 14:261-273Google Scholar
- He ZL, Wu J, O'Donnell AG, Syers JK: Seasonal responses in microbial biomass carbon, phosphorus and sulphur in soils under pasture. Biol Fertil Soils 1997, 24: 421–428. 10.1007/s003740050267View ArticleGoogle Scholar
- Hedley MJ, Stewart JWB: Method to measure microbial phosphate in soils. Soil Biol Biochem 1982, 14: 377–385. 10.1016/0038-0717(82)90009-8View ArticleGoogle Scholar
- Jenkinson DS, Brookes PC, Powlson DS: Measuring soil microbial biomass. Soil Biol Biochem 2004, 36: 5–7. 10.1016/j.soilbio.2003.10.002View ArticleGoogle Scholar
- Kaye JP, Hart SC: Competition for nitrogen between plants and soil microorganisms. Trends Ecol Evol 1997, 12: 139–143. 10.1016/S0169-5347(97)01001-XView ArticleGoogle Scholar
- Keiblinger KM, Hall EK, Wanek W, Szukics U, Hammerle I, Ellersdorfer G, Bock S, Strauss J, Sterflinger K, Richter A, Zechmeister-Boltenstern S: The effect of resource quantity and resource stoichiometry on microbial carbon-use-efficiency. FEMS Microbiol Ecol 2010, 73: 430–440.Google Scholar
- King-Salter GE: Reponse of arbuscular mycorrhizal fungi to seasonality and long-tern phosphorus fertilisation in an Irish grazed grassland. PhD Thesis, University College Dublin, Dublin, Ireland; 2008.Google Scholar
- Korsaeth A, Molstad L, Bakken LR: Modelling the competition for nitrogen between plants and microflora as a function of soil heterogeneity. Soil Biol Biochem 2001, 33: 215–226. 10.1016/S0038-0717(00)00132-2View ArticleGoogle Scholar
- Kuramae EE, Yergeau E, Wong LC, Pijl AS, van Veen JA, Kowalchuk GA: Soil characteristics more strongly influence soil bacterial communities than land-use type. FEMS Microbiol Ecol 2012, 79: 12–24. 10.1111/j.1574-6941.2011.01192.xView ArticleGoogle Scholar
- Liu L, Gundersen P, Zhang T, Mo JM: Effects of phosphorus addition on soil microbial biomass and community composition in three forest types in tropical China. Soil Biol Biochem 2012, 44: 31–38. 10.1016/j.soilbio.2011.08.017View ArticleGoogle Scholar
- Makino W, Cotner JB: Elemental stoichiometry of a heterotrophic bacterial community in a freshwater lake: implications for growth- and resource-dependent variations. Aquat Microb Ecol 2004, 34: 33–41.View ArticleGoogle Scholar
- Nannipieri P, Ciardi C, Palazzi T, Badalucco L: Short-term nitrogen reactions following the addition of urea to a grass legume association. Soil Biol Biochem 1990, 22: 549–553. 10.1016/0038-0717(90)90192-3View ArticleGoogle Scholar
- Scheu S: Automated measurement of the respiratory response of soil microcompartments: active microbial biomass in earthworm faeces. Soil Biol Biochem 1992, 24: 1113–1118. 10.1016/0038-0717(92)90061-2View ArticleGoogle Scholar
- Scheu S: Analysis of the microbial nutrient status in soil microcompartments: earthworm faeces from a basalt-limestone gradient. Geoderma 1993, 56: 575–586. 10.1016/0016-7061(93)90136-9View ArticleGoogle Scholar
- Schimel JP, Jackson LE, Firestone MK: Spatial and temporal effects on plant microbial competition for inorganic nitrogen in a California annual grassland. Soil Biol Biochem 1989, 21: 1059–1066. 10.1016/0038-0717(89)90044-8View ArticleGoogle Scholar
- Scott JT, Cotner JB, LaPara TM: Variable stoichiometry and homeostatic regulation of bacterial biomass elemental composition. Front Microbiol 2012, 3: 42. 10.3389/fmicb.2012.00042Google Scholar
- Sinsabaugh RL, Hill BH, Shah JJF: Ecoenzymatic stoichiometry of microbial organic nutrient acquisition in soil and sediment. Nature 2009, 462: U117-U795. 10.1038/nature08507View ArticleGoogle Scholar
- Tezuka Y: Bacterial regeneration of ammonium and phosphate as affected by the carbon:nitrogen:phosporus ratio of organic substrates. Microb Ecol 1990, 19: 227–238. 10.1007/BF02017167View ArticleGoogle Scholar
- Turner BL, Bristow AW, Haygarth PM: Rapid estimation of microbial biomass in grassland soils by ultra-violet absorbance. Soil Biol Biochem 2001, 33: 913–919. 10.1016/S0038-0717(00)00238-8View ArticleGoogle Scholar
- Vance ED, Brookes PC, Jenkinson DS: An extraction method for measuring soil microbial biomass-C. Soil Biol Biochem 1987, 19: 703–707. 10.1016/0038-0717(87)90052-6View ArticleGoogle Scholar
- Wang JG, Bakken LR: Competition for nitrogen during mineralization of plant residues in soil: microbial response to C and N availability. Soil Biol Biochem 1997, 29: 163–170. 10.1016/S0038-0717(96)00292-1View ArticleGoogle Scholar
- Wang YP, Law RM, Pak B: A global model of carbon, nitrogen and phosphorus cycles for the terrestrial biosphere. Biogeosciences 2010, 7: 2261–2282. 10.5194/bg-7-2261-2010View ArticleGoogle Scholar
- Watanabe FS, Olsen SR: Test of an ascorbic acid method for determining phosphorus in water and NaHCO 3 extracts from soil. Soil Sci Soc Am Proc 1965, 29: 677–678. 10.2136/sssaj1965.03615995002900060025xView ArticleGoogle Scholar
- Wu J, Joergensen RG, Pommerening B, Chaussod R, Brookes PC: Measurement of soil microbial biomass C by fumigation extraction—an automated procedure. Soil Biol Biochem 1990, 22: 1167–1169. 10.1016/0038-0717(90)90046-3View ArticleGoogle Scholar
- Zak DR, Groffman PM, Pregitzer KS, Christensen S, Tiedje JM: The vernal dam–plant microbe competition for nitrogen in northern hardwood forests. Ecology 1990, 71: 651–656. 10.2307/1940319View ArticleGoogle Scholar
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