Soil physicochemical and microbial drivers of temperature sensitivity of soil organic matter decomposition under boreal forests

Soil organic matter(SOM)in boreal forests is an important carbon sink.The aim of this study was to assess and to detect factors controlling the temperature sensitivity of SOM decomposition.Soils were collected from Scots pine,Norway spruce,silver birch,and mixed forests(O horizon)in northern Finland,and their basal respiration rates at five different temperatures(from 4 to 28℃)were measured.The Q_(10) values,showing the respiration rate changes with a 10℃ increase,were calculated using a Gaussian function and were based on temperature-dependent changes.Several soil physicochemical parameters were measured,and the functional diversity of the soil microbial communities was assessed using the MicroResp?method.The temperature sensitivity of SOM decomposition differed under the studied forest stands.Pine forests had the highest temperature sensitivity for SOM decomposition at the low temperature range(0–12℃).Within this temperature range,the Q_(10) values were positively correlated with the microbial functional diversity index(H'_(mic))and the soil C-to-P ratio.This suggested that the metabolic abilities of the soil microbial communities and the soil nutrient content were important controls of temperature sensitivity in taiga soils.     

Effect of temperature on the respiration rate of forest soil organic layer along an elevation gradient in the Polish Carpathians

The aim of our studies was to determine the relation between temperature and the respiration rate of the forest soil organic layer along an altitudinal gradient while controlling the effects of the soil characteristics. The respiration rate was measured in laboratory conditions at different temperatures, 0, 10, 20, and 30°C, in samples collected in the Polish part of the Western Carpathians at 600, 800, 1,000, and 1,200 m above sea level from four different mountains, which were later treated as replicates. The increase in the average respiration rate between two consecutive temperatures was expressed as Q ₁₀ coefficients. Among the nutrients measured in the soil organic layer, only the total organic N concentration significantly increased with elevation. The temperature effect was significant for both the respiration rate and the Q ₁₀ values. The calculated Q ₁₀ values were highest for the temperature range between 10 and 20°C, and the lowest values were obtained from the highest temperature range (20–30°C). The altitude effect was significant for the respiration rate but not for the Q ₁₀ values, indicating that the temperature sensitivity of the soil respiration did not change much along the studied altitudinal gradient.     

Decomposition of maize residues after manipulation of colonization and its contribution to the soil microbial biomass

A 28-day incubation experiment at 12°C was carried out on the decomposition of maize leaf litter to answer the questions: (1) Is the decomposition process altered by chemical manipulations due to differences in the colonization of maize leaf litter? (2) Do organisms using this maize material contribute significantly to the soil microbial biomass? The extraction of the maize straw reduced its initial microbial biomass C content by 25%. Fumigation and extraction eliminated the microbial biomass by 88%. In total, 17% of added maize straw C was mineralized to CO₂ during the 28-day incubation at 12°C in the treatment with non-manipulated straw. Only 14% of added C was mineralized in the treatment with extracted straw as well as in the treatment with fumigated and extracted straw. The net increase in microbial biomass C was 79 μg g^?1 soil in the treatment with non-manipulated straw and an insignificant 9 μg g^?1 soil in the two treatments with manipulated straw. However, the net increase did not reflect the fact that the addition of maize straw replaced an identical 58% (≈180 μg g^?1 soil) of the autochthonous microbial biomass C₃-C in all three straw treatments. In the two treatments with manipulated straw, the formation of maize-derived microbial biomass C₄-C was significantly reduced by 25%. In the three straw treatments, the ratio of fungal ergosterol-to-microbial biomass C ratio showed a constant 60% increase compared to the control, and the contents of glucosamine and muramic acid increased by 18%. The average fungal C/bacterial C ratio was 3.6 in the soil and 5.0 in the recovered maize straw, indicating that fungal dominance was not altered by the initial chemical manipulations of the maize straw-colonizing microorganisms.     

Microbial community structure mediates response of soil C decomposition to litter addition and warming

Microbial activity has been highlighted as one of the main unknowns controlling the fate and turnover of soil organic matter (SOM) in response to climate change. How microbial community structure and function may (or may not) interact with increasing temperature to impact the fate and turnover of SOM, in particular when combined with changes in litter chemistry, is not well understood. The primary aim of this study was to determine if litter chemistry impacted the decomposition of soil and litter-derived carbon (C), and its interaction with temperature, and whether this response was controlled by microbial community structure and function. Fresh or pre-incubated eucalyptus leaf litter (¹³C enriched) was added to a woodland soil and incubated at 12, 22, or 32 °C. We tracked the movement of litter and soil-derived C into CO₂, water-extractable organic carbon (WEOC), and microbial phospholipids (PLFA). The litter additions produced significant changes in every parameter measured, while temperature, interacting with litter chemistry, predominately affected soil C respiration (priming and temperature sensitivity), microbial community structure, and the metabolic quotient (a proxy for microbial carbon use efficiency [CUE]). The direction of priming varied with the litter additions (negative with fresh litter, positive with pre-incubated litter) and was related to differences in the composition of microbial communities degrading soil-C, particularly gram-positive and gram-negative bacteria, resulting from litter addition. Soil-C decomposition in both litter treatments was more temperature sensitive (higher Q₁₀) than in the soil-only control, and soil-C priming became increasingly positive with temperature. However, microbes utilizing soil-C in the litter treatments had higher CUE, suggesting the longer-term stability of soil-C may be increased at higher temperature with litter addition. Our results show that in the same soil, the growth of distinct microbial communities can alter the turnover and fate of SOM and, in the context of global change, its response to temperature.     

Priming effect of the addition of maize to a Japanese volcanic ash soil and its temperature sensitivity: a short-term incubation study

ABSTRACT

The response of soil organic matter (SOM) to global warming is a crucial subject. However, the temperature sensitivity of SOM turnover remains largely uncertain. Changes in the mineralization of native SOM, i.e., priming effect (PE) may strongly affect the temperature sensitivity of SOM turnover in the presence of global warming. We investigated the direction and magnitude of the PE in a Japanese volcanic ash soil at different temperatures (15°C, 25°C, and 35°C) using a natural ¹³C tracer (C4-plant, maize leaf) in a short-term (25 days) incubation study. In addition, we evaluated the temperature sensitivity expressed as Q₁₀ value with and without the addition of maize to the soil and their relations to PE. We found that positive PE occurred at each temperature condition and tended to increase with decreased temperature, and these PE results were consistent with the microbial biomass at the end of the incubation period. CO₂ emission from control soil (without maize) increased with increasing temperature (Q₁₀ = 2.6), but CO₂ emission from the soil with added maize did not significantly change with increasing temperature (Q₁₀ = 1.0). This was caused by the suppression of CO₂ emission from the soil with increasing temperature (Q₁₀ = 0.9). On the other hand, soil-originated CO₂ emission clearly increased with increasing temperature (Q₁₀ = 3.4) when Q₁₀ values were calculated on the assumption that the temperature and substrate supply increase at the same time (from 25°C). These results suggest that not only the temperature increase but also the labile carbon supply may be important for the temperature sensitivity of Japanese volcanic ash soil.     

Effect of warming on the temperature dependence of soil respiration rate in arctic,temperate and tropical soils

We examined the response of the temperature coefficient (Q₁₀) for soil respiration rate to changes in environmental temperature through a laboratory incubation experiment. Soil samples were collected from three climatic areas: arctic (Svalbard, Norway), temperate (Tsukuba, Japan) and tropical (Pasoh, Malaysia). The arctic and temperate soils were incubated at 8 °C (control), 12 °C (4 °C warming) and 16 °C (8 °C warming) for 17 days. The tropical soil was incubated at 16 °C (8 °C cooling), 24 °C (control) and 32 °C (8 °C warming). Before and after the incubation experiment, the temperature dependence of soil microbial respiration was measured using an open-airflow method with IRGA by changing the temperature in a water bath. The initial Q₁₀ before the incubation experiment was larger in the soils from higher latitudes: 3.4 in the arctic soil, 2.9 in the temperate soil, and 2.1 in the tropical soil. The response of the microbial respiration rate to change in temperature differed among the three soil types. The temperature dependence of respiration rate in the arctic soil did not change in response to warming by 4 and 8 °C with a Q₁₀ of about 3. On the other hand, the Q₁₀ in the temperate soil decreased with increasing incubation temperature: from 2.8 in soils incubated at 8 °C to 2.5 at 12 °C and 2.0 at 16 °C. In the tropical soil, the Q₁₀ was not changed even by the 8 °C warming with a value of 2.1, whereas the Q₁₀ was increased from 2.1 to 2.7 by the 8 °C cooling. These results suggest that the response of microbial respiration to climatic warming may differ between soils from different latitudes.     

Modeling aerobic decomposition of rice straw during the off-rice season in an Andisol paddy soil in a cold temperate region of Japan: Effects of soil temperature and moisture

Submerged rice paddies are a major source of methane (CH₄) which is the second most important greenhouse gas after carbon dioxide (CO₂). Accelerating rice straw decomposition during the off-rice season could help to reduce CH₄ emission from rice paddies during the single rice-growth season in cold temperate regions. For understanding how both temperature and moisture can affect the rate of rice straw decomposition during the off-rice season in the cold temperate region of Tohoku district, Japan, a modeling incubation experiment was carried out in the laboratory. Bulk soil and soil mixed with 2% of δ¹³C-labeled rice straw with a full factorial combination of four temperature levels (?5 to 5, 5, 15, 25°C) and two moisture levels (60% and 100% WFPS) were incubated for 24 weeks. The daily change from ?5 to 5°C was used to model the freezing–thawing cycles occurring during the winter season. The rates of rice straw decomposition were calculated by (i) CO₂ production; (ii) change in the soil organic carbon (SOC) content; and (iii) change in the δ¹³C value of SOC. The results indicated that both temperature and moisture affected the rate of rice straw decomposition during the 24-week aerobic incubation period. Rates of rice straw decomposition increased not only with high temperature, but also with high moisture conditions. The rates of rice straw decomposition were more accurately calculated by CO₂ production compared to those calculated by the change in the SOC content, or in its δ¹³C value. Under high moisture at 100% WFPS condition, the rates of rice straw decomposition were 14.0, 22.2, 33.5 and 46.2% at ?5 to 5, 5, 15 and 25°C temperature treatments, respectively. While under low moisture at 60% WFPS condition, these rates were 12.7, 18.3, 31.2 and 38.4%, respectively. The Q₁₀ of rice straw decomposition was higher between ?5 to 5 and 5°C than that between 5 and 15°C and that between 15 and 25°C. Daily freezing–thawing cycles (from ?5 to 5°C) did not stimulate rice straw decomposition compared with low temperature at 5°C. This study implies that to reduce CH₄ emission from rice paddies during the single rice-growth season in the cold temperate regions, enhancing rice straw decomposition during the high temperature period is very important.     

Relative importance of substrate type and previous soil management in synthesis of microbial biomass and substrate mineralization

Our aim was to determine whether the soil microbial biomass, which has developed naturally over many years in a given ecosystem, is specially adapted to metabolize the plant‐derived substrate C of the ecosystem within which it developed or whether the nature of recently added substrate is the more important factor. To examine this, soils from three sites in close proximity (woodland, grassland and arable from the Broadbalk Experiment at Rothamsted Research, Harpenden, UK) were each amended with air‐dried wheat straw (Triticum aestivum), ryegrass leaves (Lolium perenne) or woodland leaf litter (mainly Quercus robur and Fagus sylvatica) in a fully replicated 3 × 3 factorial laboratory experiment. The initial mineralization rates (evolved CO₂‐C) were determined during the first 6.5 hours and again, together with the amount of microbial biomass synthesized (microbial biomass C), at 7, 14, 21, 30 and 49 days of incubation. The hourly rate of CO₂‐C production during the first 6.5 hours was slowest following leaf litter addition, while the added grass gave the fastest rates of CO₂‐C evolution both within and between soils. Ryegrass addition to the arable soil led to approximately four times more CO₂‐C being evolved than when it was added to the woodland soil, at an overall rate in the arable soils of 41 μg C g^?1 soil hour^?1. In each soil, the net amounts of CO₂‐C produced were in the order grass > straw > leaf litter. In each case, the amount produced by the added leaf litter was significantly less (P < 0.05) than either the added grass or straw. Overall, the trend was for much slower rates of mineralization of all substrates in the woodland soil than in either the arable or grassland soils. During 49 days of incubation in the woodland and grassland soils, the net total amounts of CO₂‐C evolved differed significantly (P < 0.01), with grass > straw > leaf litter, respectively. In the arable soil, the amounts of CO₂‐C evolved from added grass and straw were significantly larger (P < 0.01) than from the leaf litter treatment. Our findings indicated that the amounts of CO₂‐C evolved were not related to soil management or to the size of the original biomass but to the substrate type. The amount of biomass C synthesized was also in the order grass > straw > leaf litter, at all stages of incubation in the woodland and grassland soil. In the arable soil, the same effect was observed up to 14 days, and for the rest of the incubation the biomass C synthesized was in the order grass > straw > leaf litter. Up to three times more biomass C was synthesized from the added grass than from the other substrates in all soils throughout the incubation. The maximum biomass synthesis efficiency was obtained with grass (7% of added C). Overall, the woodland soil was most efficient at synthesizing biomass C and the arable soil the least. We conclude that substrate type was the overriding factor that determined the amount of new soil microbial biomass synthesized. Mineralization of substrate C by soil microorganisms was also influenced mainly by substrate type and less by soil management or size of original biomass.     

The effects of temperature, water-filled pore space and land use on N2O emissions from an imperfectly drained gleysol

To investigate the effect of soil physical conditions and land use on emissions of nitrous oxide (N₂O) to the atmosphere, soil cores of an imperfectly drained gleysol were taken from adjacent fields under perennial ryegrass and winter wheat. The cores were fertilized with ammonium nitrate and incubated at three different temperatures and water‐filled pore space (WFPS) values, and N₂O emissions were measured by gas chromatography. Emissions showed a very large response to temperature. Apparent values of Q₁₀ (emission rate at (T + 10)°C/emission rate at T°C) for the arable soil were about 50 for the 5–12°C interval and 8.9 for 12–18°C; the corresponding Q₁₀s for the grassland soil were 3.7 and 2.3. Emissions from the grassland soil were always greater than those from the arable soil, although the ratio narrowed with increasing temperature. Changes in soil WFPS also had a profound effect on emissions. Those from the arable soil increased about 30‐fold as the WFPS increased from 60 to 80%, while that from the grassland soil increased 12‐fold. This latter response was similar to earlier field measurements. The N₂O emissions were considered to be produced primarily by denitrification. We concluded that the impacts of temperature and WFPS on emissions could both be explained on the basis of existing models relating increasing respiration or decreased oxygen diffusivity, or both, to the development of anaerobic zones within the soil.     

Temperature functions of the rate coefficients of net N mineralization in sandy arable soils. Part I. Derivation from laboratory incubations

This study aimed to experimentally determine adequate temperature functions for the rate coefficients of net N mineralization in sandy arable soils from NW Germany. Long‐term laboratory incubations were carried out in seven sandy arable soils at 3°C, 10°C, 19°C, 28°C, and 35°C in order to derive the rate coefficients of a simultaneous two‐pool first‐order kinetic equation. Thereby we differentiated between a small, fast mineralizable N pool, comprising mainly fresh residues, and a larger, slowly mineralizable N pool of old, humified organic matter. The rate coefficients were plotted against temperature, and fits of several different functions were tested: Arrhenius, Q₁₀, and multiple non‐mechanistic equations. The two derived rate coefficients showed very different temperature functions. Especially in critical temperature ranges (<5/10°C, >30/35°C) common Q₁₀ functions failed to fit well, and, only below 10°C, the Arrhenius functions were in agreement with mean measured rate coefficients. Over the studied temperature range, only relatively complex, multiple equations could adequately account for the observed patterns. In addition, temperature functions that have been derived earlier from loess soils from NW Germany were found not to be transferable to the sandy arable soils studied. Thus, the results strongly question the use of the same Arrhenius or Q₁₀ function or the same rate modifying factor for different N pools as well as for different soils as is generally done in models. Evaluations with field measurements of net N mineralization in part II of the paper (Heumann and Böttcher, 2004) will show which functions perform best in the field.     

Effect of temperature and moisture on the mineralization and humification of leaf litter in a model incubation experiment

The mineralization and humification of leaf litter collected in a mixed forest of the Prioksko-Terrasny Reserve depending on temperature (2, 12, and 22°C) and moisture (15, 30, 70, 100, and 150% of water holding capacity ( WHC)) has been studied in long-term incubation experiments. Mineralization is the most sensitive to temperature changes at the early stage of decomposition; the Q ₁₀ value at the beginning of the experiment (1.5–2.7) is higher than at the later decomposition stages (0.3–1.3). Carbon losses usually exceed nitrogen losses during decomposition. Intensive nitrogen losses are observed only at the high temperature and moisture of litter (22°C and 100% WHC). Humification determined from the accumulation of humic substances in the end of incubation decreases from 34 to 9% with increasing moisture and temperature. The degree of humification C_HA/C_FA is maximum (1.14) at 12°C and 15% WHC; therefore, these temperature and moisture conditions are considered optimal for humification. Humification calculated from the limit value of litter mineralization is almost independent of temperature, but it significantly decreases from 70 to 3% with increasing moisture. A possible reason for the difference between the humification values measured by two methods is the conservation of a significant part of hemicelluloses, cellulose, and lignin during the transformation of litter and the formation of a complex of humic substances with plant residues, where HSs fulfill a protectoral role and decrease the decomposition rate of plant biopolymers.     

Variations of SOC and MBC observed in an incubated brown loam soil managed under different tillage systems for 12 years

To assess changes in organic carbon pools, an incubation experiment was conducted under different temperatures and field moisture capacity (FMC) on a brown loam soil from three tillage practices used for 12 years: no‐till (NT), subsoiling (ST) and conventional tillage (CT). Total microbial respiration was measured for incubated soil with and without the input of straw. Results indicated that soil organic carbon (SOC) and microbial biomass carbon (MBC) under ST, NT and CT was higher in soil with straw input than that without, while the microbial quotient (MQ or MBC: SOC) and metabolic quotient (qCO₂) content under CT followed the opposite trend. Lower temperature, lower moisture and with straw input contributed to the increases in SOC concentration, especially under NT and ST systems. The SOC concentrations under ST, with temperatures of 30 and 35°C after incubation at 55% FMC, were greater than those under CT by 28.4% and 30.6%, respectively. The increase in MBC was highest at 35°C for 55%, 65% and 75% FMC; in soil under ST, MBC was greater than that under CT by 199.3%, 50.7% and 23.8%, respectively. At 30°C, the lower qCO₂ was obtained in soil incubated under NT and ST. The highest MQ among three tillage practices was measured under ST at 55% FMC, NT at 65% FMC and CT at 75% FMC with straw input. These data indicate the benefits of enhancing the MQ; the low FMC was beneficial to ST treatment. Under higher temperature and drought stress conditions, the adaptive capacity of ST and NT is better than that of CT.     

Effects of Temperature,Moisture, and Chemical Composition of Organic Substrates on C Mineralization in Soils

Laboratory experiments were conducted to (i) study the influence of chemical composition of organic substrates (green manure, rice straw, wheat straw, and farmyard manure) and temperature on carbon (C) mineralization under flooded and nonflooded moisture conditions, (ii) study the relationship between C mineralization and chemical composition of organic materials, and (iii) model C mineralization kinetics under different temperature and moisture conditions. The proportion of added C mineralized under nonflooded conditions ranged between 45 and 66% at 35 °C compared to 18 to 42% at 15 °C. Flooding the soil reduced the proportion of added C mineralized, which ranged between 25 to 47% at 35 °C and 6 to 20% at 15 °C. Water-soluble components, cellulose, lignin, and nitrogen content of the organic source significantly influenced C mineralization. Temperature sensitivity of decomposition depended on the quality of the organic substrate with relatively less decomposable farmyard manure (FYM) being more sensitive (Q₁₀ ?3.0) than the easily decomposable green manure (Q₁₀ ?2.5). A first-order monocomponent model that is based on relative rate of mineralization and includes a parameter for speed of aging best described C mineralization under both the temperature and moisture conditions. It was concluded that FYM with preponderance of recalcitrant components and low decomposability provides greater C sequestration potential than green manure and crop residues.     

Biochar amendment changes temperature sensitivity of soil respiration and composition of microbial communities 3 years after incorporation in an organic carbon-poor dry cropland soil

Topsoil samples were collected from plots in a dry cropland in the North China Plain 3 years after a single incorporation of biochar at 20 and 40 t ha^?1 and analyzed for abundances and composition of microbial community and for respiration under controlled laboratory conditions at 15, 20, and 25 °C. The addition of biochar generally reduced soil respirations at the three temperatures and the temperature sensitivity (Q₁₀) at 15–20 °C. Biochar amendment significantly increased bacterial 16S rRNA gene abundances and fungal ITS gene diversity and induced clear changes in their community compositions due to improvements in soil chemical properties such as soil organic C (SOC) and available N contents and pH. Illumina Miseq sequencing showed that the relative abundances of Actinobacteria, Gammaproteobacteria, Firmicutes, and Alternaria within Ascomycota, capable of decomposing SOC, were significantly decreased under biochar at 40 t ha^?1. The Q₁₀ values at 15–20 °C were significantly correlated with fungal diversity and dehydrogenase activity. Our results suggest that after 3 years a single biochar amendment could induce a shift in microbial community composition and functioning towards a slower organic C turnover and stability to warming, which may potentially reduce soil C loss in dryland under climate warming in the future.     

Evaluation of the rates of soil organic matter mineralization in forest ecosystems of temperate continental,mediterranean, and tropical monsoon climates

The processes of the organic matter (OM) mineralization in forest soils developed under temperate continental (Moscow oblast, Russia), Mediterranean (the central and western parts of Spain), and tropical monsoon (southern Vietnam) climates were studied under laboratory conditions. The potential and specific rates of the OM mineralization (PR _min and PR _min/C_org, respectively), the ecophysiological parameters of the microbial communities status (C_mic, qCO₂, and C_mic/C_org), and the sensitivity of the rate of the OM mineralization to the rise in temperature were evaluated by the temperature coefficients (Q ₁₀) determined in the humus horizons (0–10 cm, without forest litter). The average values of PR _min for the climatic zones decreased in the following order: Mediterranean (57.1 ± 10.6 mg C/kg per day) > temperate continental (23.8 ± 7.1 mg C/kg per day) > tropical monsoon (10.4 ± 1.6 mg C/kg per day). The lowest resistance of the soil OM to mineralization as evaluated by the PR _min/C_org values was found in the Albeluvisol and Phaeozem of the temperate continental climate and in the Acrisol of the Mediterranean climate. The highest Q ₁₀ coefficients were attributed to the OM mineralization in the forest soils of the temperate continental climate. This allowed us to conclude that the observed and expected climate changes with an increase in the mean annual air temperature should lead to the maximum intensification of the OM mineralization processes in the forest soils of northern regions.     

Driving factors of temporal variation in agricultural soil respiration

Investigations of diurnal and seasonal variations in soil respiration support modeling of regional CO₂ budgets and therefore in estimating their potential contribution to greenhouse gases. This study quantifies temporal changes in soil respiration and their driving factors in grassland and arable soils located in Northern Germany. Field measurements at an arable site showed diurnal mean soil respiration rates between 67 and 99 mg CO₂ m^–2 h^–1 with a hysteresis effect following changes in mean soil temperatures. Field soil respiration peaked in April at 5767 mg CO₂ m^–2 day^–1, while values below 300 mg CO₂ m^–2 day^–1 were measured in wintertime. Laboratory incubations were carried out in dark open flow chambers at temperatures from 5°C to 40°C, with 5°C intervals, and soil moisture was controlled at 30%, 50%, and 70% of full water holding capacity. Respiration rates were higher in grassland soils than in arable soils when the incubating temperature exceeded 15°C. The respiration rate difference between them rose with increasing temperature. Monthly median values of incubated soil respiration rates ranged from 0 to 26.12 and 0 to 7.84 µg CO₂ g^–1 dry weight h^–1, respectively, in grassland and arable land. A shortage of available substrate leads to a temporal decline in soil respiration rates, as indicated by a decrease in dissolved organic carbon. Temporal Q₁₀ values decreased from about 4.0 to below 1.5 as temperatures increased in the field. Moreover, the results of our laboratory experiments confirmed that soil temperature is the main controlling factor for the Q₁₀ values. Within the temperature interval between 20°C and 30°C, Q₁₀ values were around 2 while the Q₁₀ values of arable soils were slightly lower compared to that of grassland soils. Thus, laboratory studies may underestimate temperature sensitivity of soil respiration, awareness for transforming laboratory data to field conditions must therefore be taken into account.     

Relationship between rate of carbon dioxide evolution,microbial biomass carbon,and amount of dissolved organic carbon as affected by temperature and water content of a forest and an arable soil

Abstract

Using an Ochrept soil of a forest at climax stage or of an arable site at Kita‐Ibaraki, a city in central Japan, the rates of carbon dioxide (CO₂)‐carbon (C) evolution, the amounts of microbial biomass carbon (MBC) and the amounts of dissolved organic carbon (DOC) were measured in a laboratory with special reference to the incubation temperature and the soil water content. The rates of CO₂‐C evolution increased exponentially with increase in the incubation temperature in the range of 4–40°C. The temperature coefficients (Q₁₀) were 2.0 for the forest and 1.9 for the arable soil. The amounts of MBC were almost constant of 980 μg g^‐1 soil in the incubation temperature up to 25°C for the forest, and 340 μg g^‐1 soil in the incubation temperature up to 31 °C for the arable soil. The amounts of DOC in soil solutions were almost constant at 3.1 μg g^‐1 soil in the incubation temperature up to 25°C for the forest, and 3.8 μg g^‐1 soil in the incubation temperature up to 31°C for the arable soil. The rates of CO₂‐C evolution and the amounts of DOC increased with increase in soil water content (% of soil dry weight) up to 91% for the forest or up to 26% for the arable soil. However, the rates of CO₂‐C evolution and the amounts of DOC were almost constant within soil water content in the range of 91–160% or 26–53%, respectively. The amounts of MBC of the forest or arable soil were almost constant over a wide range of soil water content in the range of 41–220% or 8–73%, respectively. The rates of CO₂‐C evolution of both the forest and the arable soils were highly correlated with the amounts of DOC, but not with the amounts of MBC, under laboratory conditions in the case that the amounts of DOC were changed by various treatments. The regression equation,     

Respiratory quotients and Q10 of soil respiration in sub-alpine Australia reflect influences of vegetation types

Identifying and quantifying attributes that help predict rates of heterotrophic soil respiration is a key issue. Similarly, assessing the temperature sensitivity (Q₁₀) of soil C is critical to establishing if increases in Mean Annual Temperature will serve to further increase atmospheric CO₂. Using organic soils from three sub-alpine communities that differ significantly in structure, species composition and productivity, we measured the respiratory quotient (RQ = rates of CO₂ efflux/rates of O₂ uptake) and temperature sensitivity of heterotrophic respiration during long-term (120 days) incubation. As a directly measurable parameter, RQ is free of empirical assumptions and provides an additional tool that can be used in conjunction with constants derived from fitted Arrhenius or exponential equations, to help understand shifts in microbial use of C substrates and how changes in vegetation might affect soil processes. Q₁₀ did not change significantly over the course of a 120-day incubation for any of our studied soils. RQs varied with vegetation type and were consistently lower in grassland soils than woodland soils. RQs also varied during long-term incubations and declined consistently with time for grassland soils. RQs declined towards the end of the 120-day incubation for woodland soils. The generally low E_a for these soils from sub-alpine vegetation types in Australia, and the fairly rapid decline in RQ during incubation, suggest the likely greater temperature sensitivity of recalcitrant C relative to labile C could provide a strong positive feedback to increases in Mean Annual Temperature.     

Temperature and Chemical Changes During Composting of Broiler Litter

Composting broiler litter (a mixture of manure, bedding material, and wasted feed) with commonly available high-C substrates may be a viable alternative to reduce current land disposal practices for litter. Broiler litter with wood shavings as a bedding material and broiler litter with peanut hulls as a bedding material were composted with wheat straw, peanut hulls, pine bark and paper mill sludge in 0.33 m³ batch reactors. Litters and C substrates were mixed to achieve C:N ratios of approximately 30:1. Dry weight, total N, total C, temperature, electrical conductivity and pH were determined at regular intervals. Maximum temperatures peaked near 70°C within 2.25 d after mixing peanut hulls with litter and within 2.58 d for pine bark and litter. Composts made from paper mill sludge approached 50°C within 3.71 d. Wheat straw composts never exceeded 40°C which could present potential health problems associated with pathogenic microorganisms. Mass loss and C:N ratio gradually declined and stabilized approximately 84 d after mixing. Mass loss averaged 73 percent for wheat straw compost, 33 percent for peanut hull composts, and 16 percent for the other mixes. Wheat straw compost C:N ratios stabilized near 14:1 and other mixes remained above 20:1, indicating N limited conditions for complete composting. Compost pH was 5.8 after 84 d from pine bark composted with wood shaving litter and was significantly lower than pH from paper mill sludge compost with an average pH of 6.9 but similar to all other compost mixes (pH 6.7). Electrical conductivity ranged from 0.35 S m^?1 for paper mill sludge composted with wood shaving litter to 0.91 S m^?1 from wheat straw composted with peanut hull litter. Composting temperature varied considerably among C sources and all required at least 72 d of curing to stabilize the C:N ratio. Composts made from wheat straw were most effective for waste reduction but temperatures were below the 50°C level generally considered necessary to kill pathogens.     

Artificial soils to assess temperature sensitivity of the decomposition of model organic compounds: effects of chemical recalcitrance and clay‐mineral composition

Understanding the temperature sensitivity of soil organic matter (SOM) decomposition is important to predict the response of soil carbon (C) dynamics to projected global warming. There is no consensus, however, as to whether or not the decomposition of recalcitrant soil C is as sensitive to temperature as is that of labile soil C. Soil C is stabilized by three mechanisms: chemical recalcitrance, mineral interaction and physical accessibility. We used artificial soils with controlled compositions to assess the effects of chemical recalcitrance (cellulose compared with lignin) and clay‐mineral composition with montmorillonite (M) or kaolinite (K) on the decomposition of model organic compounds at 2, 12, 22 and 32°C. When only substrate composition was varied, the presence of cellulose enhanced the decomposition rate of lignin. Treatments with relatively large amounts of cellulose were very sensitive to temperature only at low temperatures (2–12°C), whereas treatments with relatively large amounts of lignin had similar temperature sensitivities at all temperatures. When only clay‐mineral composition was varied, CO₂ production rates were greatest in soils containing kaolinite‐montmorillonite mixtures (10% K:20% M) and least in soils containing kaolinite only at temperatures ≥12°C. Clay mixtures and pure montmorillonite treatments had their greatest temperature sensitivities at 2–12°C, whereas pure kaolinite treatments had the greatest temperature sensitivities at 12–22°C. Temperature sensitivities at the highest temperatures (22–32°C) were all small (Q₁₀ < 1.1 on days 30 and 140). Artificial soils with controlled but flexible compositions may serve as simple and useful models for evaluating SOM dynamics with a minimum of confounding factors.