Soil microbial biomass, activity and nitrogen transformations in a turfgrass chronosequence

Understanding the chronological changes in soil microbial properties of turfgrass ecosystems is important from both the ecological and management perspectives. We examined soil microbial biomass, activity and N transformations in a chronosequence of turfgrass systems (i.e. 1, 6, 23 and 95 yr golf courses) and assessed soil microbial properties in turfgrass systems against those in adjacent native pines. We observed age-associated changes in soil microbial biomass, CO₂ respiration, net and gross N mineralization, and nitrification potential. Changes were more evident in soil samples collected from 0 to 5 cm than the 5 to 15 cm soil depth. While microbial biomass, activity and N transformations per unit soil weight were similar between the youngest turfgrass system and the adjacent native pines, microbial biomass C and N were approximately six times greater in the oldest turfgrass system compared to the adjacent native pines. Potential C and N mineralization also increased with turfgrass age and were three to four times greater in the oldest vs. the youngest turfgrass system. However, microbial biomass and potential mineralization per unit soil C or N decreased with turfgrass age. These reductions were accompanied by increases in microbial C and N use efficiency, as indicated by the significant reduction in microbial C quotient (qCO₂) and N quotient (qN) in older turfgrass systems. Independent of turfgrass age, microbial biomass N turnover was rapid, averaging approximately 3 weeks. Similarly, net N mineralization was ∼12% of gross mineralization regardless of turfgrass age. Our results indicate that soil microbial properties are not negatively affected by long-term management practices in turfgrass systems. A tight coupling between N mineralization and immobilization could be sustained in mature turfgrass systems due to its increased microbial C and N use efficiency.     

Soil microbial biomass and nitrogen dynamics in a turfgrass chronosequence: A short-term response to turfgrass clipping addition

A mechanistic understanding of soil microbial biomass and N dynamics following turfgrass clipping addition is central to understanding turfgrass ecology. New leaves represent a strong sink for soil and fertilizer N, and when mowed, a significant addition to soil organic N. Understanding the mineralization dynamics of clipping N should help in developing strategies to minimize N losses via leaching and denitrification. We characterized soil microbial biomass and N mineralization and immobilization turnover in response to clipping addition in a turfgrass chronosequence (i.e. 3, 8, 25, and 97 yr old) and the adjacent native pines. Our objectives were (1) to evaluate the impacts of indigenous soil and microbial attributes associated with turf age and land use on the early phase decomposition of turfgrass clippings and (2) to estimate mineralization dynamics of turfgrass clippings and subsequent effects on N mineralization of indigenous soils. We conducted a 28-d laboratory incubation to determine short-term dynamics of soil microbial biomass, C decomposition, N mineralization and nitrification after soil incorporation of turfgrass clippings. Gross rates of N mineralization and immobilization were estimated with ¹⁵N using a numerical model, FLAUZ. Turfgrass clippings decomposed rapidly; decomposition and mineralization equivalent to 20-30% of clipping C and N, respectively, occurred during the incubation. Turfgrass age had little effect on decomposition and net N mineralization. However, the response of potential nitrification to clipping addition was age dependent. In young turfgrass systems having low rates, potential nitrification increased significantly with clipping addition. In contrast, old turfgrass systems having high initial rates of potential nitrification were unaffected by clipping addition. Isotope ¹⁵N modeling showed that gross N mineralization following clipping addition was not affected by turf age but differed between turfgrass and the adjacent native pines. The flush of mineralized N following clipping addition was derived predominantly from the clippings rather than soil organic N. Our data indicate that the response of soil microbial biomass and N mineralization and immobilization to clipping addition was essentially independent of indigenous soil and microbial attributes. Further, increases in microbial biomass and activity following clipping addition did not stimulate the mineralization of indigenous soil organic N.     

Soil microbial biomass, activity and potential nitrogen mineralization in a pasture: Impact of stock camping activity

Grazing animals recycle a large fraction of ingested C and N within a pasture ecosystem, but the redistribution of C and N via animal excreta is often heterogeneous, being highest in stock camping areas, i.e., near shade and watering sources. This non-uniform distribution of animal excreta may modify soil physical and chemical attributes, and likely affect microbial community eco-physiology and soil N cycling. We determined microbial population size, activity, N mineralization, and nitrification in areas of a pasture with different intensity of animal excretal deposits (i.e., stock camping, open grazing and non-grazing areas). The pasture was cropped with coastal bermudagrass (Cynodon dactylon L.) and subjected to grazing by cattle for 4 y. Soil microbial biomass, activity and N transformations were significantly higher at 0-5 cm than at 5-15 cm soil depth, and the impacts of heterogeneous distribution of animal excreta were more pronounced in the uppermost soil layer. Microbial biomass, activity and potential net N mineralization were greater in stock camping areas and were significantly correlated (r²≈0.50, P<0.05) with the associated changes in total soil C and N. However, gross N mineralization and nitrification potential tended to be lower in stock camping areas than in the open grazing areas. The lower gross N mineralization, combined with greater net N mineralization in stock camping areas, implied that microbial N immobilization was lower in those areas than in the other areas. This negative association between microbial N immobilization and soil C is inconsistent with a bulk of publications showing that microbial N immobilization was positively related to the amount of soil C. We hypothesized that the negative correlation was due to microbial direct utilization of soluble organic N and/or changes in microbial community composition towards active fungi dominance in stock camping areas.     

Microbial biomass and C and N transformations in forest floors under European beech, sessile oak, Norway spruce and Douglas-fir at four temperate forest sites

The purpose of this research was to compare soil chemistry, microbially mediated carbon (C) and nitrogen (N) transformations and microbial biomass in forest floors under European beech (Fagus sylvatica L.), sessile oak (Quercus petraea (Mattuschka) Lieblein), Norway spruce (Picea abies (L.) Karst) and Douglas-fir (Pseudotsuga menziesii (Mirbel) Franco) at four study sites. We measured soil chemical characteristics, net N mineralization, potential and relative nitrification, basal respiration, microbial and metabolic quotient and microbial biomass C and N under monoculture stands at all sites (one mixed stand). Tree species affected soil chemistry, microbial activities and biomass, but these effects varied between sites. Our results indicated that the effect of tree species on net N mineralization was likely to be mediated through their effect on soil microbial biomass, reflecting their influence on organic matter content and carbon availability. Differences in potential nitrification and relative nitrification might be related to the presence of ground vegetation through its influence on soil NH₄ and labile C availability. Our findings highlight the need to study the effects of tree species on microbial activities at several sites to elucidate complex N cycle interactions between tree species, ground vegetation, soil characteristics and microbial processes.     

Microbial biomass and activity in soil and litter underPinus sylvestris, Picea abies andBetula pendula at originally similar field afforestation sites

Microbial biomass C and N, and activities related to C and N cycles, were compared in needle and leaf litter, and in the uppermost 10 cm of soil under the litter layer in Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies L.) and silver birch (Betula pendula L.) stands, planted on originally similar field afforestation sites 23–24 years ago. The ground vegetation was differentiated under different tree species, consisting of grasses and herbs under birch and pine, and mosses or no vegetation with a thick layer of needles under spruce. The C:N ratio of the soils was 13–21 and the soil pH_{CaCl 2} 3.8–5.2. Both showed little variation under different tree species. Microbial biomass C and N, C mineralization, net ammonification, reduction) did not differ significantly in soil under different tree species either. Birch leaf litter had a higher pH_{CaCl 2} (5.9) than spruce and pine needle litter (pH 5.0 and 4.8, respectively). The C:N ratio of spruce needles was 30, and was considerably higher in pine needles (69) and birch leaves (54). Birch leaves tended to have the highest microbial biomass C and C mineralization. Spruce needles appeared to have the highest microbial biomass N and net formation of mineral N, whereas formation of mineral N in pine needles and birch leaves was negligible. Microbial biomass C and N were of the same order of magnitude in the soil and litter samples but C mineralization was tenfold higher in the litter samples.     

Microbial biomass and activity in soil and litter underPinus sylvestris, Picea abies andBetula pendula at originally similar field afforestation sites

Microbial biomass C and N, and activities related to C and N cycles, were compared in needle and leaf litter, and in the uppermost 10 cm of soil under the litter layer in Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies L.) and silver birch (Betula pendula L.) stands, planted on originally similar field afforestation sites 23–24 years ago. The ground vegetation was differentiated under different tree species, consisting of grasses and herbs under birch and pine, and mosses or no vegetation with a thick layer of needles under spruce. The C:N ratio of the soils was 13–21 and the soil pH_{CaCl 2} 3.8–5.2. Both showed little variation under different tree species. Microbial biomass C and N, C mineralization, net ammonification, reduction) did not differ significantly in soil under different tree species either. Birch leaf litter had a higher pH_{CaCl 2} (5.9) than spruce and pine needle litter (pH 5.0 and 4.8, respectively). The C:N ratio of spruce needles was 30, and was considerably higher in pine needles (69) and birch leaves (54). Birch leaves tended to have the highest microbial biomass C and C mineralization. Spruce needles appeared to have the highest microbial biomass N and net formation of mineral N, whereas formation of mineral N in pine needles and birch leaves was negligible. Microbial biomass C and N were of the same order of magnitude in the soil and litter samples but C mineralization was tenfold higher in the litter samples.     

Earthworms increase soil microbial biomass carrying capacity and nitrogen retention in northern hardwood forests

Earthworms have been shown to produce contrasting effects on soil carbon (C) and nitrogen (N) pools and dynamics. We measured soil C and N pools and processes and traced the flow of ¹³C and ¹⁵N from sugar maple (Acer saccharum Marsh.) litter into soil microbial biomass and respirable C and mineralizable and inorganic N pools in mature northern hardwood forest plots with variable earthworm communities. Previous studies have shown that plots dominated by either Lumbricus rubellus or Lumbricus terrestris have markedly lower total soil C than uncolonized plots. Here we show that total soil N pools in earthworm colonized plots were reduced much less than C, but significantly so in plots dominated by contain L. rubellus. Pools of microbial biomass C and N were higher in earthworm-colonized (especially those dominated by L. rubellus) plots and more ¹³C and ¹⁵N were recovered in microbial biomass and less was recovered in mineralizable and inorganic N pools in these plots. These plots also had lower rates of potential net N mineralization and nitrification than uncolonized reference plots. These results suggest that earthworm stimulation of microbial biomass and activity underlie depletion of soil C and retention and maintenance of soil N pools, at least in northern hardwood forests. Earthworms increase the carrying capacity of soil for microbial biomass and facilitate the flow of N from litter into stable soil organic matter. However, declines in soil C and C:N ratio may increase the potential for hydrologic and gaseous losses in earthworm-colonized sites under changing environmental conditions.     

Response of soil C and N transformations to tannin fractions originating from Scots pine and Norway spruce needles

Tannins are polyphenolic compounds that may influence litter decomposition, humus formation, nutrient (especially N) cycling and ultimately, plant nutrition and growth. The aim of this study was to determine the response of C and N transformations in soil to tannins of different molecular weight from Norway spruce (Picea abies (L.) Karst) and Scots pine (Pinus sylvestris L.) needles, tannic acid and cellulose. Arginine was added to test whether the soil microbial community was limited by the amount of N, and arginine+tannin treatments were used to test whether the effects of tannins could be counteracted by adding N. Soil and needle samples were taken from adjacent 70-year-old Scots pine and Norway spruce stands located in Kivalo, northern Finland. Tannins were extracted from needles and fractioned based on molecular weight; the fractions were then characterized by LC-MS and GC-MS. Light fractions contained tannin monomers and dimers as well as many other compounds, whereas heavy fractions consisted predominantly of polymerized condensed tannins. Spruce needles contained more procyanidin than prodelphinidin units, while in pine needles prodelphinidin units seemed to be dominant. The fractions were added to soil samples, pine fractions to pine soil and spruce fractions to spruce soil, and incubated at 14 °C for 6 weeks. CO₂ evolution was followed throughout the experiment, and the rates of net mineralization of N and net nitrification, concentration of dissolved organic N (DON) and amounts of microbial biomass C and N were measured at the end of the experiment. The main effects of the fractions were similar in both soils. Light fractions strongly enhanced respiration and decreased net N mineralization, indicating higher immobilization of N in the microbial biomass. On the contrary, heavy fractions reduced respiration and slightly increased net N mineralization, suggesting toxic or protein-precipitating effects. The effects of tannic acid and cellulose resembled those of light fractions. DON concentrations generally decreased during incubation and were lower with heavy fractions than with light fractions. No clear differences were detected between the effects of light and heavy fractions on microbial biomass C and N. Treatments that included addition of arginine generally showed trends similar to treatments without it, although some differences between light and heavy fractions became more obvious with arginine than without it. Overall, light fractions seemed to act as a labile source of C for microbes, while heavy fractions were inhibitors.     

How do coniferous needle tannins influence C and N transformations in birch humus layer?

The aim of this study was to explore the response of C and N transformations in the humus layer under silver birch (Betula pendula Roth) to compounds, especially condensed tannins, of different molecular weight extracted and fractioned from Norway spruce (Picea abies (L.) Karst) and Scots pine (Pinus sylvestris L.) needles. Lighter fractions containing tannin monomers and dimers as well as many other compounds, and heavier fractions consisting predominantly of polymerized condensed tannins, were added to samples taken from the humus layer of birch stand. The effects of the spruce and pine fractions were mostly similar, but some differences in magnitude were observed; our results indicated that lighter fractions of pine were easier for microbes to degrade and use than lighter fractions of spruce. Lighter fractions of both tree species increased soil respiration and decreased net N mineralization, while heavier fractions inhibited respiration and increased net N mineralization. Microbial biomass C was not clearly affected by any of the treatments, but with some of the pine fractions the amount of N in the microbial biomass was increased. Comparison of the effects of fractions in birch and in spruce and pine soils, which were studied earlier, showed no major differences between the effects of the fractions in birch and in their own soils, but gave some indication of adaptation.     

Microbial activity and nutrient dynamics in earthworm casts (Lumbricidae)

Summary Microbial respiration, microbial biomass and nutrient requirements of the microflora (C, N, P) were studied in the food substrate (soil taken from the upper 3 cm of the mineral soil of a beech wood on limestone), the burrow walls and the casts of the earthworm Aporrectodea caliginosa (Savigny). The passage of the soil through the gut caused an increase in soil microbial respiration of about 90% over a 4-week period. Microbial biomass was increased only in freshly deposited casts and decreased in aging faeces to a level about 10% lower than in soil. Microbial respiration of the burrow walls was only increased over a shorter period (about 2 weeks). The microflora of the soil and the burrow walls was limited by P, whereas in earthworm casts, microbial growth was limited by the amount of available C. In aging faeces the P requirement of the microflora increased and approached that of the soil. Immobilization of phosphate in earthworm casts is probably caused by mainly abiotic processes. C mineralization by soil microflora fertilized with glucose and P was limited by N, except in freshly deposited casts. Ammonium, not nitrate, was responsible for this process. N dynamics in earthworm casts are discussed.     

Microbial activities in forest floor layers under silver birch, Norway spruce and Scots pine

The aim of this study was to compare microbial activities in the litter (L), fermentation (F) and humified (H) layers of the forest floor under silver birch (Betula pendula Roth), Norway spruce (Picea abies (L.) Karst) and Scots pine (Pinus sylvestris L.). Soil pH, C-to-N ratio, respiration rates, concentration of NH₄-N, net N mineralization and nitrification rates, gross NH₄⁺ production and consumption rates and amounts of C (C_mic) and N (N_mic) in the microbial biomass were determined from samples taken from the L, F and H layers under silver birch, Norway spruce and Scots pine. The forest floors under birch and spruce were more active than that under pine, having higher respiration and net N mineralization rates, and higher C_mic and N_mic values than pine forest floor. Differences between tree species were smaller in the H layer than in the L and F layers. The L layer had the highest rates of respiration for all tree species, while rates of net N mineralization were highest in the F layer for birch and spruce. Pine showed negligible net N mineralization in all layers. Concentration of NH₄-N was the best predictor of rate of net N mineralization (r=0.748). In general, C_mic and N_mic were higher in the L and F layers than in the H layer, as were their relative proportions of total C (C_tot) and N (N_tot), respectively. C_mic correlated positively with soil respiration (r=0.980) and N_mic with concentration of NH₄-N (r=0.915).     

Volatile monoterpenes in soil atmosphere under birch and conifers: Effects on soil N transformations

The aim of this study was to examine the occurrence and concentrations of volatile organic compounds (VOCs), in particular, volatile monoterpenes, in soil atmosphere under silver birch (Betula pendula L.) and two conifers, Norway spruce (Picea abies (L.) Karst.) and Scots pine (Pinus sylvestris L.), and to determine the effects of the most relevant monoterpenes on transformations of soil N. The study site was a 70-year-old tree species experiment in Kivalo, northern Finland. VOCs were collected using two methods, passive air samplers and a chamber method. In soil atmosphere under spruce and especially under pine, the concentrations of monoterpenes were high, α- and β-pinene, Δ-3-carene and myrcene being the most abundant compounds, whereas concentrations of monoterpenes in soil atmosphere under birch were negligible. Samples of humus layer from the birch stand incubated in vitro and exposed to vapors from monoterpenes typical of coniferous forest soil showed decreased rates of net N mineralization but simultaneously increased rates of C mineralization. The response of soil microbial biomass C and N to different monoterpenes varied, but some monoterpenes considerably decreased soil microbial biomass. Altogether these results suggest that these compounds have negative effects on soil N transformations, but may serve as carbon and energy source for part of soil microbes.     

Regulation of microbial carbon,nitrogen, and phosphorus transformations by temperature and moisture during decomposition of <Emphasis Type="Italic">Calluna vulgaris</Emphasis> litter

To evaluate the effect of climate change on ecosystem functioning, the temperature and moisture response of microbial C, N, and P transformations during decomposition of Calluna vulgaris (L.) Hull. litter was studied in a laboratory incubation experiment. The litter originated from a dry heathland in the Netherlands where P limited vegetation growth. Fresh litter was incubated at 5, 10, 15, or 20°C and at a moisture content of 50, 100, or 200% in a full factorial design. Microbial nutrient transformations and activity were evaluated during two successive periods: an initial period of 48 days characterized by microbial growth and a second period from 48 to 206 days in which microbial growth declined significantly. Temperature and moisture response of respiration rate, the metabolic quotient (qCO₂), C, N, and P immobilization, net N and P mineralization and nitrification rates were evaluated by performing linear regressions. Microbial nutrient transformations and microbial activity depended both on temperature and moisture. In the first period, the respiration rate, qCO₂, microbial C and N immobilization, net P mineralization, net N mineralization and net nitrification rates were more strongly affected by temperature, while the microbial P immobilization rate was more strongly affected by moisture. The respiration rate, qCO₂, P immobilization rate, net P and N mineralization rate, and nitrification rate increased with temperature and moisture, while the C and N immobilization rate decreased with increasing temperature and increased with moisture. In the second period, C, N, and P immobilization and net N and P mineralization rates were significantly lower. The respiration rate and qCO₂ continued to increase with temperature and moisture, but C and N immobilization rates increased with temperature and declined with increasing moisture. Net P mineralization rate decreased at higher temperature and moisture, and nitrification rate declined with increasing temperature and increased with moisture. It was concluded that plant growth in these P-limited systems is very sensitive to climate change as it strongly relies on the competition for P with microbes, and temperature and moisture have a large effect on the immobilization rate of available P.     

Substrate type,temperature, and moisture content affect gross and net N mineralization and nitrification rates in agroforestry systems

Accurate prediction of soil N availability requires a sound understanding of the effects of environmental conditions and management practices on the microbial activities involved in N mineralization. We determined the effects of soil temperature and moisture content and substrate type and quality (resulting from long-term pasture management) on soluble organic C content, microbial biomass C and N contents, and the gross and net rates of soil N mineralization and nitrification. Soil samples were collected at 0–10 cm from two radiata pine (Pinus radiata D. Don) silvopastoral treatments (with an understorey pasture of lucerne, Medicago sativa L., or ryegrass, Lolium perenne L.) and bare ground (control) in an agroforestry field experiment and were incubated under three moisture contents (100, 75, 50% field capacity) and three temperatures (5, 25, 40 °C) in the laboratory. The amount of soluble organic C released at 40 °C was 2.6- and 2.7-fold higher than the amounts released at 25 °C and 5 °C, respectively, indicating an enhanced substrate decomposition rate at elevated temperature. Microbial biomass C:N ratios varied from 4.6 to 13.0 and generally increased with decreasing water content. Gross N mineralization rates were significantly higher at 40 °C (12.9 g) than at 25 °C (3.9 g) and 5 °C (1.5 g g^–1 soil day^–1); and net N mineralization rates were also higher at 40 °C than at 25 °C and 5 °C. The former was 7.5-, 34-, and 29-fold higher than the latter at the corresponding temperature treatments. Gross nitrification rates among the temperature treatments were in the order 25 °C >40 °C >5 °C, whilst net nitrification rates were little affected by temperature. Temperature and substrate type appeared to be the most critical factors affecting the gross rates of N mineralization and nitrification, soluble organic C, and microbial biomass C and N contents. Soils from the lucerne and ryegrass plots mostly had significantly higher gross and net mineralization and nitrification rates, soluble organic C, and microbial biomass C and N contents than those from the bare ground, because of the higher soil C and N status in the pasture soils. Strong positive correlations were obtained between gross and net rates of N mineralization, between soluble organic C content and the net and gross N mineralization rates, and between microbial biomass N and C contents.     

Nitrogen mineralization and microbial activity in permanent pastures amended with nitrogen fertilizer or dung

 Gross rates of soil processes and microbial activity were measured in two grazed permanent pasture soils which had recently been amended with N fertilizer or dung. ¹⁵N studies of rates of soil organic matter turnover showed gross N mineralization was higher, and gross N immobilization was lower, in a long-term fertilized soil than in a soil which had never received fertilizer N. Net mineralization was also found to be higher in the fertilized soil: a consequence of the difference between the opposing N turnover processes of N mineralization and immobilization. In both soils without amendments the soil microbial biomass contents were similar, but biomass activity (specific respiration) was higher in the fertilized soil. Short-term manipulation of fertilizer N input, i.e. adding N to unfertilized soil, or witholding N from previously fertilized soil, for one growing season, did not affect gross mineralization, immobilization or biomass size and activity. Amendments of dung had little effect on gross mineralization, but there was an increase in immobilization in both soils. Total biomass also increased under dung in the unfertilized soil, but specific respiration was reduced, suggesting changes in the composition of the biomass. Dung had a direct effect on the microbial biomass by temporarily increasing available soil C. Prolonged input of fertilizer N increases soil C indirectly as a result of enhanced plant growth, the effect of which may not become evident within one seasonal cycle. Received: 18 December 1998     

Drivers of microbial respiration and net N mineralization at the continental scale

The dominant pools of C and N in the terrestrial biosphere are in soils, and understanding what factors control the rates at which these pools cycle is essential in understanding soil CO₂ production and N availability. Many previous studies have examined large scale patterns in decomposition of C and N in plant litter and organic soils, but few have done so in mineral soils, and fewer have looked beyond ecosystem specific, regional, or gradient-specific drivers. In this study, we examined the rates of microbial respiration and net N mineralization in 84 distinct mineral soils in static laboratory incubations. We examined patterns in C and N pool sizes, microbial biomass, and process rates by vegetation type (grassland, shrubland, coniferous forest, and deciduous/broadleaf forest). We also modeled microbial respiration and net N mineralization in relation to soil and site characteristics using structural equation modeling to identify potential process drivers across soils. While we did not explicitly investigate the influence of soil organic matter quality, microbial community composition, or clay mineralogy on microbial process rates in this study, our models allow us to put boundaries on the unique explanatory power these characteristics could potentially provide in predicting respiration and net N mineralization. Mean annual temperature and precipitation, soil C concentration, microbial biomass, and clay content predicted 78% of the variance in microbial respiration, with 61% explained by microbial biomass alone. For net N mineralization, only 33% of the variance was explained, with mean annual precipitation, soil C and N concentration, and clay content as the potential drivers. We suggest that the high R² for respiration suggests that soil organic matter quality, microbial community composition, and clay mineralogy explain at most 22% of the variance in respiration, while they could explain up to 67% of the variance in net N mineralization.     

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.     

Carbon mineralization is promoted by phosphorus and reduced by nitrogen addition in the organic horizon of northern hardwood forests

Limitations to the respiratory activity of heterotrophic soil microorganisms exert important controls of CO₂ efflux from soils. In the northeastern US, ecosystem nutrient status varies across the landscape and changes with forest succession following disturbance, likely impacting soil microbial processes regulating the transformation and emission of carbon (C). We tested whether nitrogen (N) or phosphorus (P) limit the mineralization of soil organic C (SOC) or that of added C sources in the Oe horizon of successional and mature northern hardwood forests in three locations in central New Hampshire, USA. Added N reduced mineralization of C from SOC and from added leaf litter and cellulose. Added P did not affect mineralization from SOC; however, it did enhance mineralization of litter- and cellulose- C in organic horizons from all forest locations. Added N increased microbial biomass N and K₂SO₄-extractable DON pools, but added P had no effect. Microbial biomass C increased with litter addition but did not respond to either nutrient. The direction of responses to added nutrients was consistent among sites and between forest ages. We conclude that in these organic horizons limitation by N promotes mineralization of C from SOC, whereas limitation by P constrains mineralization of C from new organic inputs. We also suggest that N suppresses respiration in these organic horizons either by relieving the N limitation of microbial biomass synthesis, or by slowing turnover of C through the microbial pool; concurrent measures of microbial growth and turnover are needed to resolve this question.     

Nitrogen immobilization and mineralization during initial decomposition of15N-labelled pea and barley residues

The immobilization and mineralization of N following plant residue incorporation were studied in a sandy loam soil using¹⁵N-labelled field pea (Pisum sativum L.) and spring barley (Hordeum vulgare L.) straw. Both crop residues caused a net immobilization of soil-derived inorganic N during the complete incubation period of 84 days. The maximum rate of N immobilization was found to 12 and 18 mg soil-derived N g^?1 added C after incorporation of pea and barley residues, respectively. After 7 days of incubation, 21% of the pea and 17% of the barley residue N were assimilated by the soil microbial biomass. A comparison of the¹⁵N enrichments of the soil organic N and the newly formed biomass N pools indicated that either residue N may have been assimilated directly by the microbial biomass without entering the soil inorganic N pool or the biomass had a higher preference for mineralized ammonium than for soil-derived nitrate already present in the soil. In the barley residue treatment, the microbial biomass N was apparently stabilized to a higher degree than the biomass N in the pea residue treatment, which declined during the incubation period. This was probably due to N-deficiency delaying the decomposition of the barley residue. The net mineralization of residue-derived N was 2% in the barley and 22% in the pea residue treatment after 84 days of incubation. The results demonstrated that even if crop residues have a relative low C/N ratio (15), transient immobilization of soil N in the microbial biomass may contribute to improved conservation of soil N sources.     

Carbon and nitrogen turnover in two acid forest soils of southeast Australia as affected by phosphorus addition and drying and rewetting cycles

The effects of adding P and of drying and rewetting were studied in two acid forest soils from southeast Australia. The soils were a yellow podzolic with a low soil organic matter content (3.75% C) and a red earth with a high organic matter content (13.5% C). C and N mineralization and microbial C and N contents were investigated in a laboratory incubation for 151 days. Microbial C and N were estimated by a hexanol fumigation-extraction technique. Microbial C was also determined by substrate-induced respiration combined with a selective inhibition technique to separate the fungal and the bacterial biomass. The results obtained by the selective inhibition technique were not conclusive. Adding P to the soil and drying and rewetting the soil reduced microbial N. This effect was more pronounced in rapidly and frequently dried soils. Microbial C was generally less affected by these treatments. Compared with the control, the addition of P caused a reduction in respiration in the red earth (-13%) but an increase in the yellow podzolic soil (+12%). In the red earth net N mineralization was highest following the addition of P. In the yellow podzolic soil highest N mineralization rates were obtained when the soil was subjected to drying and rewetting cycles. In both soils increased N mineralization was associated with a decrease in microbial N, indicating that the mineralized N was of microbial origin. Nitrification decreased with rapid drying and rewetting. The addition of P promoted heterotrophic nitrification in both soils.