Effects of liming on carbon and nitrogen mineralization in coniferous forests

A temporary decline in tree growth has often been observed after liming in coniferous forests poor in N but seldom in forests rich in N. To test the hypothesis that the decline was caused by decreases in N supply, C and N mineralization were estimated in incubated soil: (1) after liming in the laboratory, and (2) after earlier liming in the field. Liming increased the C mineralization rate in needle litter, nor humus and 0 to 5 cm mineral soil for a period of 40 to 100 days at 15°C. After that period, liming had no effect on the CO₂ evolution rate in materials poor in N (C:N ratios 30 to 62) but increased the CO₂ evolution rate in materials rich in N (C:N ratios 24 to 28). When liming induced nitrification, the CO₂ evolution rate was reduced. Liming resulted in lower net N mineralization rate in needle litter and mor humus. The reduction was more pronounced when NH₄ ⁺ was the only inorganic form than when NO₃ ^? was the predominant form. The reason is probably that chemical fixation of NH₃ and amino compounds increases with increasing pH. Because of the fixation, the incubation technique most likely underestimated the mineralized N available to the roots. Taking this underestimation into consideration, liming initially reduced the N release in the litter layer. In the other soil layers, liming increased the N release in soils rich in N and had only small effects in soils poor in N. For the total N supply to the roots in the litter, humus and 0 to 5 cm mineral soil layers, liming caused a slight reduction in soils poor in N and a slight increase in soils rich in N. Data on tree growth corresponded with these results.The hypotheses that tree growth depressions can be caused by reduced N supply after liming and that tree growth increases can be caused by increased N supply after liming thus seem reasonable.     

Effects of acidification and liming on carbon and nitrogen mineralization and soil organisms in mor humus

The aim was to determine if changes in C and N mineralization after acidification and liming could be explained by changes in the soil organism biomass. Intact soil cores from F/H layers in a Norway spruce (C:N=31) and a Scots pine (C:N=44) stand in central Sweden were treated in the laboratory for 55 days with deionized water (control), weak H₂SO₄ (successively applied as 72 mm of acid rain of pH 3.1), strong H₂SO₄ (applied as a single high dose of pH 1), and lime CaCO₃. Strong acidification reduced C mineralization and increased net N mineralization in both soils. Weak acidification resulted in similar but less pronounced effects. Liming initially stimulated C mineralization rate, but the rates declined, indicating that an easily available C source was successively used up by the microorganisms. Liming also increased net N mineralization in the C:N=31 humus, but not significantly in the C:N--44 humus. Strong acidification generally affected the amounts of FDA-active fungal hyphae, nematodes and enchytraeids more than the other treatments did. The increases in net N mineralization after acidification and liming could only partly be explained by the decreases in biomass N in soil organisms. Mineralization of biomass N from killed soil organisms could at the most explain up to about 30% of the increase in net N mineralization after strong acidification. Most of the effects on N mineralization seemed to depend on the fact that acidification reduced and liming increased the availability of C and N to the microorganisms. Furthermore, acidification seemed to reduce the incorporation of N from dead organisms into the soil organic matter and, thereby, make the N compounds more readily available to microbial decomposition and mineralization.     

Effect of liming on some chemical,biochemical, and microbiological properties of acid soils under spruce (Picea abies L.)

Summary Soil pH, total organic C, total N, exchangeable Al, available P, CO₂ evolution, microbial biomass C and N, phosphatase and dehydrogenase activities were determined in acid soils sampled under spruce subjected to acid deposition, before and after liming. A slight decrease in pH values was observed from the edge of a tree canopy to the base of the trunk in acid soils. Liming drastically reduced exchangeable Al and increased CO₂ evolution, microbial biomass, and the metabolic quotient. The microbial biomass C to total organic C ratio increased after liming but did not reach 2%, the average value considered valid in soils where the C content is in equilibrium, that is when C inputs are equal to C outputs. The microbial biomass C:N ratio decreased after liming, thus indicating that bacteria became predominant over fungi when soil acidity decreased. Dehydrogenase activity but not phosphatase activity was increased by liming. The decrease in phosphatase activity was not completely related to the increase in available P, but was also dependent on microbial growth and the decrease in acid phosphatase, the predominant component of acid soils.     

Pools and fluxes of carbon and nitrogen in 40-year-old forest liming experiments in Southern Sweden

Soil samples were collected from litter, humus and mineral soil layers to a depth of 50 cm in 37–42 year-old limed and unlimed plots in one beech and three spruce stands in S Sweden for determination of carbon (C) and nitrogen (N) pools, C and N mineralization rates and nitrification rates. The samples were sifted while still fresh and incubated at a constant temperature (15°C) and soil moisture (50 % WHC) for 110–180 days with periodic subsamplings. The C and N pools in the uppermost soil layers were significantly lower in plots limed with 9–10 t CaCO₃ ha^?1 than in unlimed plots, whereas the pools in the deeper mineral soil did not differ markedly between the treatments. In the whole soil profile, the C and N pools had, on average, decreased by 16% (P<0.05) and 11% (P>0.05), respectively, after 40 yrs. The smaller reduction in N pools resulted in significantly lower C:N ratios and increased N immobilization in the limed spruce plots but not in the limed beech plot. C and net N mineralization rates were increased in some of the limed plots and decreased in others. This indicates that liming can still have a stimulatory effect after 40 yrs in some soils. The nitrification potential was increased in the limed plots. Liming did not increase tree growth in the stands investigated. We conclude that liming with high doses of CaCO₃ is likely to reduce pools of soil C and possibly even soil N in relation to unlimed areas in spruce and beech forests in S Sweden. If trees in limed stands do not respond with better growth, the treatment will thus result in a net ecosystem loss of C and N in relation to unlimed areas. It was not possible to conclude whether the effects of low doses of lime would be similar to those of high doses.     

Nitrogen mineralization and nitrifier activity in limed and urea‐treated soils

Abstract

The effect of liming on mineralization and soil nitrifier activity (NA) was investigated with Brookston clay (pH 5.7) and Haldimand clay (pH 4.7). Liming increased the rate of mineralization in both soils but at a rate about 4‐times greater in Haldimand clay than Brookston clay. A significant increase in N mineralization due to liming occurred in both soils only when pH was raised above 6.0. The rate of mineralization was greater than nitrification in the Haldimand soil resulting in NH₄ ⁺ accumulation. Nitrifier activity increased with liming of Brookston clay, but decreased in Haldimand clay after 15 days of incubation. There was a significant increase in nitrifier activity due to liming from 15 to 60 days in Haldimand clay. After 60 days nitrifier activity in limed treatments increased by five times over the unlimed control.

The nitrification of urea powder (1000 mg N.kg^‐1) mixed into the soil was also studied in several soils incubated at 15°C for 28 days. There was evidence up to 14 days that nitrification of urea was correlated with initial nitrifier activity. Between 14 and 28 days, other factors such as soil pH and possible ammonia toxicity in coarser textured soils as well as nitrifier activity were important. Accumulation of nitrite occurred mainly in soils with a pH above 7.0 up to 28 days especially where nitrifier population enrichment was not done.     

Litter quality effects on soil carbon and nitrogen dynamics in temperate alley cropping systems

Microcosm and litterbag experiments were conducted to determine the effects of litter quality, soil properties and microclimate differences on soil carbon (C) and nitrogen (N) mineralization in alley cropping systems. Bulk soils were collected from 0 to 20 cm depth at three sites: a 21-year old pecan (Carya illinoinensis)/bluegrass (Poa trivialis) intercrop (Pecan site) in north-central Missouri, a 12-year old silver maple (Acer saccharinum)/soybean (Glycine max)–maize (Zea mays) rotation (Maple site) in northeastern Missouri and a restored prairie site (MDC site) in southwestern Missouri. Seven tree and crop litters with varying composition were collected, including pecan, silver maple, chestnut and walnut leaf litter (tree litter) and maize, soybean and bluegrass residues (crop litter). Aerobic microcosm incubations were maintained at 25 °C and a soil water potential of −47 kPa. Unamended MDC soil mineralized 24 and 18% more CO₂ than the Pecan and Maple soils, respectively. Soil amended with crop litter mineralized on average 32% more CO₂ than when amended with tree litter. Net N mineralization from soybean litter was 40 mg kg⁻¹, while all other litter immobilized N for various durations. A double pool and a single pool model best described C and N mineralization from amended soils, respectively. Cumulative CO₂ mineralized, labile C fraction (C₁) and potentially mineralizable C (C₀) were correlated to litter total N and lignin contents and to (lignin + polyphenol):N ratio. In the field, bluegrass litter decomposed and released N twice as fast as pecan leaf litter. Soybean, maize and silver maple litter released 84, 75 and 63% of initial N, respectively, 308 days after field placement, while no differences in mass loss was observed among the three litter materials. At the Maple site, mass and N remaining, 308 days after field placement was lower at the middle of the alley, corresponding to higher soil temperature and water content. No differences in mass loss and N release patterns were observed at the Pecan site. Microclimate and litter quality effects can lead to differences in nutrient availability in alley cropping systems.     

Nitrogen fertilization and liming increased CO2 and N2O emissions from tropical ferralsols,but not from a vertisol

The application of nitrogen (N) fertilizers and liming (CaCO₃) to improve soil quality and crop productivity are regarded as effective and important agricultural practices. However, they may increase greenhouse gas (GHG) emissions. There is limited information on the GHG emissions of tropical soils, specifically when liming is combined with N fertilization. We therefore conducted a full factorial laboratory incubation experiment to investigate how N fertilizer (0 kg N ha⁻¹, 12.5 kg N ha⁻¹ and 50 kg N ha⁻¹) and liming (target pH = 6.5) affect GHG emissions and soil N availability. We focussed on three common acidic soils (two ferralsols and one vertisol) from Lake Victoria (Kenya). After 8 weeks, the most significant increase in cumulative carbon dioxide (CO₂) and nitrous oxide (N₂O) fluxes compared with the unfertilized control was found for the two ferralsols in the N + lime treatment, with five to six times higher CO₂ fluxes than the control. The δ¹³C signature of soil-emitted CO₂ revealed that for the ferralsols, liming (i.e. the addition of CaCO₃) was the dominant source of CO₂, followed by urea (N fertilization), whereas no significant effect of liming or of N fertilization on CO₂ flux was found for the vertisol. In addition, the N₂O fluxes were most significantly increased by the high N + lime treatment in the two ferralsols, with four times and 13 times greater N₂O flux than that of the control. No treatment effects on N₂O fluxes were observed for the vertisol. Liming in combination with N fertilization significantly increased the final nitrate content by 14.5%–39% compared with N fertilization alone in all treatment combinations and soils. We conclude that consideration should be given to the GHG budgets of agricultural ferralsols since liming is associated with high liming-induced CO₂ and N₂O emissions. Therefore, nature-based and sustainable sources should be explored as an alternative to liming in order to manage the pH and the associated fertility of acidic tropical soils.     

Fumigation-extraction and substrate-induced respiration derived microbial biomass C,and respiration rate in limed soil of Scots pine sapling stands

The effect of liming on microbial biomass C and respiration activity was studied in four liming experiments on young pine plantations. One of the experimental sites had been limed and planted 12 years before, two 5 years before, and one a year before soil sampling. The youngest experimental site was also treated with ash fertilizer. Liming raised the pH_KCl of the humus layer by 1.5 units or less. Microbial biomass was measured using the fumigation-extraction and substrate-induced respiration methods. Liming did not significantly affect microbial biomass C, except in the experiment which had been limed 11 years ago, where there was a slight biomass increase. Basal respiration, which was measured by the evolution of CO₂, increased in the limed soils, except for the youngest experiment, where there was no effect. Ash fertilization raised the soil pH_KCl by about 0.5 unit, but did not influence microbial biomass C or basal respiration. Fumigation-extraction and substrate-induced respiration derived microbial biomass C values were correlated positively with each other (r=0.65), but substrate-induced respiration gave approximately 1.3 times higher results. In addition, the effect of storing the soil samples at +6 and -18°C was evaluated. The effects were variable but, generally, the substrate-induced respiration derived microbial biomass C decreased, and the fumigation-extraction derived microbial biomass C and basal respiration decreased or were not affected by storage.     

Organic matter characteristics and C and N transformations in the humus layer under two tree species, Betula pendula and Picea abies

The aim of this study was to compare the effects of silver birch (Betula pendula Roth) and Norway spruce (Picea abies (L.) Karst.) on soil C and N transformations and on the characteristics of organic matter. Soil samples were taken from the humus layer of a replicated 35-year-old birch-spruce field experiment growing on Vaccinium myrtillus site type in middle-eastern Finland. The soil was a podzol and humus type mor. Soil pH was higher under birch (4.7) than under spruce (4.1). The C-to-N ratio was lower under birch (17) than under spruce (23). Per unit organic matter, microbial biomass C and N, net N mineralization and net nitrification were all higher in birch soil than in spruce soil. The rate of C mineralization (CO₂ production) was, however, the same regardless of tree species. Water-extracts were analyzed for the concentrations of dissolved organic C (DOC) and N (DON) and characterized according to molecular size distribution by ultrafiltration and according to chemical composition using a resin fractionation technique. The concentration of DON, in particular, was higher in birch soil than in spruce soil. The distribution of DOC and DON into different fractions based on molecular size or chemical composition was rather similar in both soils. The concentration of total phenolics, expressed as tannic acid equivalents, was higher in the humus layer under birch than in the humus layer under spruce, because the birch humus layer contained significantly more low-molecular weight (about <0.5 kD) phenolics than the spruce humus layer did. The concentration of proanthocyanidins (condensed tannins) was higher in spruce soil than in birch soil. The concentrations of the five most abundant phenolic acids showed that ferulic and p-coumaric acids were more abundant in spruce soil. Birch soil tended to contain slightly more nonvolatile sesquiterpenes than the spruce soil. The concentration of diterpenes was similar in both soils; but birch soil contained significantly more triterpenes, mainly sterols, than spruce soil did.     

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.     

The effect of Siberian tree species on the mineralization rate of soil organic matter

The mineralization of organic matter in the soils under the six main Siberian forest-forming species was studied. The nitrogen mineralization and nitrification were the most affected by the different tree species. The rate of the CO₂ formation was similar in the soils under the different tree species. The factors affecting the variation of the data characterizing the microbiological processes were revealed. The nitrogen mineralization and nitrification correlated with the contents of the soil carbon, nitrogen, and NH₄⁺ and the soil acidity, while the carbon mineralization correlated only with the NH₄⁺ concentration and the C/N ratio.     

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.     

Liming effects on some chemical and biological parameters of soil (spodosols and histosols) in a hardwood forest watershed

Acidic lakes and streams can be restored with base application (usually limestone) provided that the base does not wash out before the benefits of alkalization can be realized; liming soils of the adjoining watershed may be an alternative approach. This study was conducted to provide a scientific basis for soil liming. Plots (50 m²) with different limestone dosages (e.g. 0, 5, 10 or 15 Mg CaCO₃ ha^?1) were established on each of two different soils (a Spodosol and a Histosol) in the Woods Lake watershed of the Adirondack Park Region of New York, USA. Six months after soil liming much of the added limestone was still present in both the Spodosol and in the Histosol. Ten months after soil liming results indicated that: (1) soil pH increased (>1 unit) but mostly in the top 1 cm; (2) net N mineralization increased from 9.6 to ca. 15 µg N g^?1 d^?1 and nitrification increased from 2.8 to ca. 8 µg N g^?1 d^?1; (3) denitrification was not affected (98 µg N g^?1 d^?1); (4) CO₂ production potential decreased in the surface soil and as a function of limestone dosage (60 to 6 µmol g^?1 d^?1); and (5) soluble SO ₄ ^2? concentrations in the Histosol were not affected (105 µmol L^?1). Liming acidic forest soils with >5 Mg CaCO₃ ha^?1 may increase the soil's acid neutralizing capacity, which could provide long-term benefits for surface water acidification.     

C and N turnover in structurally intact soils of different texture

The turnover of native and applied C and N in undisturbed soil samples of different texture but similar mineralogical composition, origin and cropping history was evaluated at −10 kPa water potential. Cores of structurally intact soil with 108, 224 and 337 g clay kg⁻¹ were horizontially sliced and ¹⁵N-labelled sheep faeces was placed between the two halves of the intact core. The cores together with unamended treatments were incubated in the dark at 20 °C and the evolution of CO₂-C determined continuously for 177 d. Inorganic and microbial biomass N and ¹⁵N were determined periodically. Net nitrification was less in soil amended with faeces compared with unamended soil. When adjusted for the NO₃-N present in soil before faeces was applied, net nitrification became negative indicating that NO₃-N had been immobilized or denitrified. The soil most rich in clay nitrified least N and ¹⁵N. The amounts of N retained in the microbial biomass in unamended soils increased with clay content. A maximum of 13% of the faeces ¹⁵N was recovered in the microbial biomass in the amended soils. CO₂-C evolution increased with clay content in amended and unamended soils. CO₂-C evolution from the most sandy soil was reduced due to a low content of potentially mineralizable native soil C whereas the rate constant of C mineralization rate peaked in this soil. When the pool of potentially mineralizable native soil C was assumed proportional to volumetric water content, the three soils contained similar proportions of potentially mineralizable native soil C but the rate constant of C mineralization remained highest in the soil with least clay. Thus although a similar availability of water in the three soils was ensured by their identical matric potential, the actual volume of water seemed to determine the proportion of total C that was potentially mineralizable. The proportion of mineralizable C in the faeces was similar in the three soils (70% of total C), again with a higher rate constant of C mineralization in the soil with least clay. It is hypothesized that the pool of potentially mineralizable C and C rate constants fluctuate with the soil water content.     

Forest biogeochemistry interactions among greenhouse gases and N deposition

Interactions between N deposition and the fluxes between atmosphere and forest ecosystems of the greenhouse gases CO₂, CH₄ and N₂O are examined. It is argued that forest productivity has increased due to increased N deposition since the industrial revolution in areas where N has been limiting to forest production. It is shown that most boreal and large parts of temperate forests growing on mineral soils are N limited still today. The increased above ground production due to improved N availability seems to result in an equal sized build-up of the C pool of at least boreal forest soils, in the first place in the humus layer. This is explained by an increased litter production of needles and roots and a decreased decomposition rate in an N rich environment. N deposition thus contributes to reduce the atmospheric levels of CO₂. In areas where N is still limiting forest growth, a decreased N deposition, thus, logically, would result in decreased forest productivity and act as a source of increased CO₂ levels to the atmosphere. Increased N deposition results in decreased CH₄ oxidation of forest mineral soils and thus, acts to increase the greenhouse effect. However, this mechanism expressed as greenhouse contribution probably is small in relation to the reduction caused by increased CO₂ fixation. From most forest mineral soils there seem to be small rates of N₂O formation independently of deposition rates.     

Effects of Liming and Fertilization (N,PK) on Chemistry and Nitrogen Turnover in Acidic Forest Soils in SW Sweden

SW Sweden has very acidic forest soils because of deposition ofair-borne pollutants. Large-scale liming and fertilization have been proposed as countermeasures against a possible future development of forest decline. To test the effects of suggested treatments, liming (3 or 6 t ha¹) and fertilization with easily soluble PK (25 or 50 kg P, 80 or 160 kg K ha¹) or N(20 kg N ha¹ annually in the form of NH₄ NO₃) were applied in different combinations in four experiments in 30–60 yr-old Picea abies forests in SW Sweden. Four yearsafter the initial application of the fertilizers, samples were taken from the O-horizon and the two uppermost 5 cm thick layersof the mineral soil. Their pH(H₂O) and easily extractable Ca, Mg, K, P and inorganic N contents were analyzed. Samples werealso incubated to estimate net N mineralization and potential nitrification rates. Liming increased the pH by 0.6–1 unit in the O-horizon, and by 0.1 unit in the mineral soil. The Ca + Mg content increased by 15–25 kmol_c ha¹ (4–8 foldincrease) in the O-horizon of the limed plots, while an increaseof 5 kmol_c ha¹ (two-fold increase) was observed in theuppermost 5 cm of the mineral soil. Liming did not affect extractable P, K or inorganic N contents. Net N mineralization and potential nitrification rates in the O-horizon were enhanced 1.5- and 6-fold, respectively, by liming, but it had no apparenteffect in the mineral soil. N fertilization caused a slight increase (1.5 kg ha¹) in the content of inorganic N, buthad no effects on the other variables measured. The amount ofextractable P was raised by 16 kg ha¹ in plots given the high P dose (50 kg ha¹), but no other effects of PK fertilization were detected.     

Soil warming and liming impacts on the recovery of 15N in an acidic soil under soybean cropping

Liming has important implications for N dynamics in acidic soils planted with legumes that are not fully understood. We used a ¹⁵N tracer (K¹⁵NO₃) to examine N dynamics in a Chromic Luvisol planted with soybean with and without lime in environmentally‐controlled chambers set at 20°C and 30°C (full factorial design). Liming increased total N and ¹⁵N recovery in soybean, but had no effect on microbial recovery. Elevated temperature, increased total plant N, decreased ¹⁵N recovery in soybean and microbes, and increased loss of N through leaching. Our results show enhanced uptake of soil mineral N by soybean with liming, thereby reducing N loss from soil, while an increase in temperature from 20°C to 30°C may enhance N loss in these systems.     

Microbial community structure and characteristics of the organic matter in soils under Pinus sylvestris, Picea abies and Betula pendula at two forest sites

 Microbial biomass C (C_mic), C mineralization rate, phospholipid fatty acid (PLFA) profiles and community level physiological profiles (CLPPs) using Biolog were determined from the humus and mineral soil layers in adjacent stands of Scots pine (Pinus sylvestris L.), Norway spruce [Picea abies (L.) Karst.] and silver birch (Betula pendula Roth) at two forest sites of different fertility. In addition, the Fourier-transformed infrared (FTIR) spectra were run on the samples for characterization of the organic matter. C_mic and C mineralization rate tended to be lowest under spruce and highest under birch, at the fertile site in all soil layers and at the less fertile site in the humus layer. There were also differences in microbial community structure in soils under different tree species. In the humus layer the PLFAs separated all tree species and in the mineral soil spruce was distinct from pine and birch. CLPPs did not distinguish microbial communities from the different tree species. The FTIR spectra did not separate the tree species, but clearly separated the two sites. Received: 3 December 1999     

Effects of temperature,glucose and inorganic nitrogen inputs on carbon mineralization in a Tibetan alpine meadow soil

High levels of available nitrogen (N) and carbon (C) have the potential to increase soil N and C mineralization. We hypothesized that with an external labile C or N supply alpine meadow soil will have a significantly higher C mineralization potential, and that temperature sensitivity of C mineralization will increase. To test the hypotheses an incubation experiment was conducted with two doses of N or C supply at temperature of 5, 15 and 25 °C. Results showed external N supply had no significant effect on CO₂ emission. However, external C supply increased CO₂ emission. Temperature coefficient (Q₁₀) ranged from 1.13 to 1.29. Significantly higher values were measured with C than with N addition and control treatment. Temperature dependence of C mineralization was well-represented by exponential functions. Under the control, CO₂ efflux rate was 425 g CO₂–C m^?2 year^?1, comparable to the in situ measurement of 422 g CO₂–C m^?2 year^?1. We demonstrated if N is disregarded, microbial decomposition is primarily limited by lack of labile C. It is predicted that labile C supply would further increase CO₂ efflux from the alpine meadow soil.     

Relationships of soil respiration to microbial biomass, substrate availability and clay content

The roles of microbial biomass (MBC) and substrate supply as well as their interaction with clay content in determining soil respiration rate were studied using a range of soils with contrasting properties. Total organic C (TOC), water-soluble organic carbon, 0.5 M K₂SO₄-extractable organic C and 33.3 mM KMnO₄-oxidisable organic carbon were determined as C availability indices. For air-dried soils, these indices showed close relationship with flush of CO₂ production following rewetting of the soils. In comparison, MBC determined with the chloroform fumigation-extraction technique had relatively weaker correlation with soil respiration rate. After 7 d pre-incubation, soil respiration was still closely correlated with the C availability indices in the pre-incubated soils, but poorly correlated with MBC determined with three different techniques—chloroform fumigation extraction, substrate-induced respiration, and chloroform fumigation-incubation methods. Results of multiple regression analyses, together with the above observations, suggested that soil respiration under favourable temperature and moisture conditions was principally determined by substrate supply rather than by the pool size of MBC. The specific respiratory activity of microorganisms (CO₂-C/MBC) following rewetting of air-dried soils or after 7 d pre-incubation was positively correlated with substrate availability, but negatively correlated with microbial pool size. Clay content had no significant effect on CO₂ production rate, relative C mineralization rate (CO₂-C/TOC) and specific respiratory activity of MBC during the first week incubation of rewetted dry soils. However, significant protective effect of clay on C mineralization was shown for the pre-incubated soils. These results suggested that the protective effect of clay on soil organic matter decomposition became significant as the substrate supply and microbial demand approached to an equilibrium state. Thereafter, soil respiration would be dependent on the replenishment of the labile substrate from the bulk organic C pool.