Soil N transformations after application of 15N‐labeled biomass in incubation experiments with repeated soil drying and rewetting

The effects of repeated soil drying and rewetting on microbial biomass N (N_bio) and mineral N (N_min) were measured in incubation experiments simulating typical moisture and temperature conditions for soils from temperate climates in the post‐harvest period. After application of in vitro ¹⁵N‐labeled fungal biomass to a silty loam, one set of soils was exposed to two drying‐rewetting cycles (treatment DR; 14 days to decrease soil moisture to 20 % water‐holding capacity (WHC) and subsequently 7 days at 60 % WHC). A control set (treatment CM) was kept at constant moisture conditions (60 % WHC) throughout the incubation. N_bio and N_min as well as the ¹⁵N enrichment of these N pools were measured immediately after addition of ¹⁵N‐labeled biomass (day 0) and after each change in soil moisture (day 14, 21, 35, 42). Drying and rewetting (DR) resulted in higher N_min levels compared to CM towards the end of the incubation. Considerable amounts of N_bio were susceptible to mineralization as a result of soil drying (i.e., drying enhanced the turnover of N_bio), and significantly lower N_bio values were found for DR at the end of each drying period. Immediately after biomass incorporation into the soil (day 0), 22 % of the applied ¹⁵N was found in the N_min pool. Some of this ¹⁵N_min must have been derived from dead cells of the applied microbial biomass as only about 80 % of the microbes in the biomass suspension were viable, and only 52 % of the ¹⁵N_bio was extractable (using the fumigation‐extraction method). The increase in ¹⁵N_min was higher than for unlabeled N_min, indicating that added labeled biomass was mineralized with a higher rate than native biomass during the first drying period. Overall, the effect of drying and rewetting on soil N turnover was more pronounced for treatment DR compared to CM during the second drying‐rewetting cycle, resulting in a higher flush of mineralization and lower microbial biomass N levels.     

Effect of drying and rewetting on phosphorus transformations in red brown soils with different soil organic matter content

In this study, the effect of drying and rewetting on native P transformations in two red brown soils with different management history was investigated. Three treatments, T1 (constantly moist), T2 (dried for 4 days and then kept dry), T3 (rewetted after 4 days drying) were used. Drying and rewetting caused a rapid increase in microbial P (Pm) and labile organic P (labile Po) within 1 day and a gradual increase in available inorganic P (Colwell). These increases were only temporarily, as Pm and labile Po decreased with time and were at the same level as in the constantly moist soil by the end of the incubation period of 21 days. The effect of drying and rewetting on P transformations strongly depended on soil organic matter content, being more pronounced in the soil with high organic matter content, compared to the soil with low soil organic matter content.     

Modelling soil organic matter decomposition and rainfall erosion in two tropical soils after forest clearing for permanent agriculture

A soil organic matter turnover model has been developed to analyse soil carbon (soil organic-C) loss caused by organic matter decomposition and rainfall erosion in soils used for permanent cultivation. It has been used to build up model profiles of five soils, one occurring in temperate and four in tropical regions, on the basis of estimates for ‘natural’ organic matter input. Organic matter input data for different systems of cultivation were used to model the long-term decomposition of soil organic-C in these model profiles. The modelling results show that soil organic matter decomposition in the tropics is three to four times faster than in temperate regions, and that there is a marked influence of soil type and soil climate. Simulated losses of organic-C in the tropical soils, not accounting for erosion are 31 to 50 per cent after 50 years and 43 to 63 per cent after 100 years of continuous cultivation. The simulated loss of soil organic-C when rainfall erosion is also allowed for is 40 to 80 per cent. Erosion caused an extra loss of at least 7 per cent after 100 years. The initial input of charcoal from forest burning is lost through erosion at a rate of 50 to almost 100 per cent, depending on the severity of erosion. The sensitivity of modelling results to variations in input data was also analysed. The losses of soil carbon were also used to calculate the global flux of CO₂ from soils. Soils are probably a small but not negligible source of CO₂.     

Repeated drying–rewetting cycles and their effects on the emission of CO2, N2O,NO, and CH4 in a forest soil

Prolonged summer droughts due to climate change are expected for this century, but little is known about the effects of drying and wetting on biogenic trace‐gas fluxes of forest soils. Here, the response of CO₂, N₂O, NO, and CH₄ fluxes from temperate forest soils towards drying–wetting events has been investigated, using undisturbed soil columns from a Norway spruce forest in the “Fichtelgebirge”, Germany. Two different types of soil columns have been used for this study to quantify the contribution of organic and mineral horizons to the total fluxes: (1) organic horizons (O) and (2) organic and mineral soil horizons (O+M). Three drying–wetting treatments with different rewetting intensities (8, 20, and 50 mm of irrigation d^–1) have been compared to a constantly moist control to estimate the influence of rainfall intensity under identical drying conditions and constant temperature (+15°C). Drought significantly reduced CO₂, N₂O, and NO fluxes in most cycles. Following rewetting, CO₂ fluxes quickly recovered back to control level in the O columns but remained significantly reduced in the O+M columns with total CO₂ fluxes from the drying–wetting treatment ranging approx. 80% of control fluxes. Fluxes of N₂O and NO remained significantly reduced in both O and O+M columns even after rewetting, with cumulative fluxes from drying–wetting treatments ranging between 20% and 90% of the control fluxes, depending on gas and cycle. Fluxes of CH₄ were small in all treatments and seem to play no significant role in this soil. No evidence for the release of additional gas fluxes due to drying–wetting was found. The intensity of rewetting had no significant effect on the CO₂, N₂O, NO, and CH₄ fluxes, suggesting that the length of the drought period is more important for the emission of these gases. We can therefore not confirm earlier findings that fluxes of CO₂, N₂O, and NO during wetting of dry soil exceed the fluxes of constantly moist soil.     

Episodic rewetting enhances carbon and nitrogen release from chaparral soils

The short-term pulse of carbon (C) and nitrogen (N) mineralization that accompanies the wetting of dry soils may dominate annual C and N production in many arid and semi-arid environments characterized by seasonal transitions. We used a laboratory incubation to evaluate the impact of short-term fluctuations in soil moisture on long-term carbon and nitrogen dynamics, and the degree to which rewetting enhances C and N release. Following repeated drying and rewetting of chaparral soils, cumulative CO₂ release in rewet soils was 2.2-3.7 times greater than from soils maintained at equivalent mean soil moisture and represented 12-18% of the total soil C pool. Rewetting frequency did not affect cumulative CO₂ release but did enhance N turnover, and net N mineralization and nitrification increased with rewetting in spite of significant reductions in nitrification potential. Litter addition decreased inorganic N release but enhanced dissolved organic nitrogen (DON) and dissolved organic carbon (DOC) from dry soils, indicating the potential importance of a litter-derived pulse to short-term nutrient dynamics.     

The proportional mineralisation of microbial biomass and organic matter caused by air-drying and rewetting of a grassland soil

During the first few days after rewetting of an air-dried soil (AD-RW), microbial activity increases compared to that in the original moist soil, causing increased mineralisation (a flush) of soil organic carbon (C) and other nutrients. The AD-RW flush is believed to be derived from the enhanced mineralisation of both non-biomass soil organic matter (due to its physical release and enhanced availability) and microbial biomass killed during drying and rewetting. Our aim was to determine the effects of AD-RW on the mineralisation of soil organic matter and microbial biomass during and after repeated AD-RW cycles and to quantify their proportions in the CO₂-C flushes that resulted. To do this, a UK grassland soil was amended with ¹⁴C-labelled glucose to label the biomass and then given five AD-RW cycles, each followed by 7 d incubation at 25 °C and 50% water holding capacity. Each AD-RW cycle increased the amount of CO₂-C evolved (varying from 83 to 240 μg g⁻¹ soil), compared to the control with, overall, less CO₂-C being evolved as the number of AD-RW cycles increased. In the first cycle, the amount of biomass C decreased by 44% and microbial ATP by 70% while concentrations of extractable C nearly doubled. However, all rapidly recovered and within 1.3 d after rewetting, biomass C was 87% and ATP was 78% of the initial concentrations measured prior to air-drying. Similarly, by 2 d, extractable organic C had decreased to a similar concentration to the original. After the five AD-RW cycles, the amounts of total and ¹⁴C-labelled biomass C remaining in the soil accounted for 60 and 40% of those in the similarly incubated control soil, respectively. Soil biomass ATP concentrations following the first AD-RW cycle remained remarkably constant (ranging from about 10 to 14 μmol ATP g⁻¹ biomass C) and very similar to the concentration in the fresh soil prior to air-drying. We developed a simple mathematical procedure to estimate the proportion of CO₂-C derived from biomass C and non-biomass C during AD-RW. From it, we estimate that, over the five AD-RW cycles, about 60% of the CO₂-C evolved came from mineralisation of non-biomass organic C and the remainder from the biomass C itself.     

Determination of the fate of regularly applied 13C‐labeled‐artificial‐exudates C in two agricultural soils

Exudates are part of the total rhizodeposition released by plant roots to soil and are considered as a substantial input of soil organic matter. Exact quantitative data concerning the contribution of exudates to soil C pools are still missing. This study was conducted to reveal effects of ¹³C‐labeled exudate (artificial mixture) which was regularly applied to upper soil material from two agricultural soils. The contribution of exudate C to water‐extractable organic C (WEOC), microbial biomass C (MBC), and CO₂‐C evolution was investigated during a 74 d incubation. The WEOC, MBC, and CO₂‐C concentrations and the respective δ¹³C values were determined regularly. In both soils, significant incorporation of artificial‐exudate‐derived C was observed in the WEOC and MBC pool and in CO₂‐C. Up to approx. 50% of the exudate‐C amounts added were recovered in the order WEOC << MBC < CO₂‐C in both soils at the end of the incubation. Newly built microbial biomass consisted mainly of exudates, which substituted soil‐derived C. Correspondingly, the CO₂‐C evolved from exudate‐treated soils relative to the controls was dominated by exudate C, showing a preferential mineralization of this substrate. Our results suggest that the remaining 50% of the exudate C added became stabilized in non‐water‐extractable organic fractions. This assumption was supported by the determination of the total organic C in the soils on the second‐last sampling towards the end of the incubation. In the exudate‐treated soils, significantly more soil‐derived C compared to the controls was found in the WEOC on almost all samplings and in the MBC on the first sampling. This material might have derived from exchange processes between the added exudate and the soil matrix. This study showed that easily available substrates can be stabilized in soil at least in the short term.     

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.     

Soil organic matter dynamics in grassland soils under elevated CO2: Insights from long-term incubations and stable isotopes

Elevated atmospheric carbon dioxide (CO₂) levels generally stimulate carbon (C) uptake by plants, but the fate of this additional C largely remains unknown. This uncertainty is due in part to the difficulty in detecting small changes in soil carbon pools. We conducted a series of long-term (170-330 days) laboratory incubation experiments to examine changes in soil organic matter pool sizes and turnover rates in soil collected from an open-top chamber (OTC) elevated CO₂ study in Colorado shortgrass steppe. We measured concentration and isotopic composition of respired CO₂ and applied a two-pool exponential decay model to estimate pool sizes and turnover rates of active and slow C pools. The active and slow C pools of surface soils (5-10 cm depth) were increased by elevated CO₂, but turnover rates of these pools were not consistently altered. These findings indicate a potential for C accumulation in near-surface soil C pools under elevated CO₂. Stable isotopes provided evidence that elevated CO₂ did not alter the decomposition rate of new C inputs. Temporal variations in measured δ¹³C of respired CO₂ during incubation probably resulted mainly from the decomposition of changing mixtures of fresh residue and older organic matter. Lignin decomposition may have contributed to declining δ¹³C values late in the experiments. Isotopic dynamics during decomposition should be taken into account when interpreting δ¹³C measurements of soil respiration. Our study provides new understanding of soil C dynamics under elevated CO₂ through the use of stable C isotope measurements during microbial organic matter mineralization.     

Compaction effects on CO2 and N2O production during drying and rewetting of soil

The effects of compaction on soil porosity and soil water relations are likely to influence substrate availability and microbial activity under fluctuating soil moisture conditions. We conducted a short laboratory incubation to investigate the effects of soil compaction on substrate availability and biogenic gas (CO₂ and N₂O) production during the drying and rewetting of a fine-loamy soil. Prior to initiating the drying and wetting treatments, CO₂ production (−10 kPa soil water content) from uncompacted soil was 2.3 times that of compacted soil and corresponded with higher concentrations of microbial biomass C (MBC) and dissolved organic C (DOC). In contrast, N₂O production was 67 times higher in compacted than uncompacted soil at field capacity. Soil aeration rather than substrate availability (e.g. NO₃⁻ and DOC) appeared to be the most important factor affecting N₂O production during this phase. The drying of compacted soil resulted in an initial increase in CO₂ production and a nearly two-fold higher average rate of C mineralization at maximum dryness (owing to a higher water-filled pore space [WFPS]) compared to uncompacted soil. During the drying phase, N₂O production was markedly reduced (by 93-96%) in both soils, though total N₂O production remained slightly higher in compacted than uncompacted soil. The increase in CO₂ production during the first 24 h following rewetting of dry soil was about 2.5 times higher in uncompacted soil and corresponded with a much greater release of DOC than in compacted soil. MBC appeared to be the source of the DOC released from uncompacted soil but not from compacted soil. The production of N₂O during the first 24 h following rewetting of dry soil was nearly 20 times higher in compacted than uncompacted soil. Our results suggest that N₂O production from compacted soil was primarily the result of denitrification, which was limited by substrates (especially NO₃⁻) made available during drying and rewetting and occurred rapidly after the onset of anoxic conditions during the rewetting phase. In contrast, N₂O production from uncompacted soil appeared to be primarily the product of nitrification that was largely associated with an accumulation of NO₃⁻ following rewetting of dry soil. Irrespective of compaction, the response to drying and rewetting was greater for N₂O production than for CO₂ production.     

Effect of repeated drying at different temperatures on soil organic matter decomposition and characteristics,and on the soil microflora

Samples of a slightly acid sand soil were subjected to frequently repeated cycles of drying (85 or 30°C), moistening and incubation (29°C, 4 weeks). During about 60 cycles the loss of carbon, as CO₂, from the samples dried at 85°C, 30°C and the undried ones was found to be 31.2, 18.0 and 17.0%. respectively. A complete depletion of degradable material was not achieved after 60 drying-wetting cycles. After 60 cycles the 85 C-samplcs still showed the highest CO₂-production.The microbial population was reduced in numbers and species in all samples. The highest numbers of bacteria and fungi were found in the samples originally dried at 85°C. However, only a relative low proportion of these microorganisms could grow on less easily accessible substrates.Data on changes in the pH and on the C/N ratio of the organic matter are discussed, together with possible ways in which organic matter becomes available during heating.     

Responses of carbon,nitrogen and phosphorus to two consecutive drying–rewetting cycles in soils

Drying and rewetting cycles are known to be important for the dynamics of carbon (C), phosphorus (P), and nitrogen (N) in soils. This study reports the short‐term responses of these nutrients to consecutive drying and rewetting cycles and how varying soil moisture content affects microbial biomass C and P (MBC and MBP), as well as associated carbon dioxide (CO₂) and nitrous oxide (N₂O) emissions. The soil was incubated for 14 d during which two successive drying–rewetting episodes were imposed on the soils. Soils subjected to drying (DRW) were rewetted on the seventh day of each drying period to return them to 60% water holding capacity, whilst continually moist samples (M), with soil maintained at 60% water holding capacity, were used as control samples. During the first seven days, the DRW samples showed significant increases in extractable ammonium, total oxidized nitrogen, and bicarbonate extractable P concentrations. Rewetting after the first drying event produced significant increases only in CO₂ flux (55.4 µg C g^?1 d^?1). The MBC and MBP concentrations fluctuated throughout the incubation in both treatments and only the second drying–rewetting event resulted in a significantly MBC decrease (416.2 and 366.8 mg kg^?1 in M and DRW soils, respectively). The two drying–rewetting events impacted the microbial biomass, but distinguishing the different impacts of microbial versus physical impacts of the perturbation is difficult. However, this study, having a combined approach (C, N, and P), indicates the importance of understanding how soils will react to changing patterns of drying–rewetting under future climate change.     

Effect of repeated drying-wetting-freezing-thawing cycles on the active soil organic carbon pool

Samples of soddy-podzolic soil (long-term overgrown fallow and continuous bare fallow), gray forest soil (forest, farming agrocenosis), and a typical chernozem (virgin steppe, forest area, farming agrocenosis, continuous bare fallow) have been incubated under stable conditions; other samples of these soils have been subjected to six drying-wetting-incubation-freezing-thawing-incubation cycles during 136 days. The wetting of dried soils and the thawing of frozen soils result in an abrupt but short increase in the emission rate of C-CO₂ by 2.7–12.4 and 1.6–2.7 times, respectively, compared to the stable incubation conditions. As the soil is depleted in potentially mineralizable organic matter, the rate of the C-CO₂ emission pulses initiated by disturbing impacts decreases. The cumulative extra production of C-CO₂ by soils of natural lands for six cycles makes up 21–40% of that in the treatments with stable incubation conditions; the corresponding value for cultivated soils, including continuous clean fallow, is in the range of 45–82%. The content of potentially mineralizable organic matter in the soils subjected to recurrent drying-wetting-freezingthawing cycles decreased compared to the soils without disturbing impacts by 1.6–4.4 times, and the mineralization constants decreased by 1.9–3.6 times. It has been emphasized that the cumulative effect of drying-wetting-freezing-thawing cycles is manifested not only in the decrease in the total Corg from the soil but also in the reduction of the mineralization potential of the soil organic matter.     

The influence of clay on the rate of decay of amino acid metabolites synthesized in soils during decomposition of cellulose

¹⁴C-labelled cellulose was added to seven different soils containing silt + clay (particles < 0.02 mm) in amounts which varied from 8 to 75 per cent. The cellulose was allowed to decompose, and the amounts of labelled C transformed into metabolites hydrolyzable into amino acids were determined. The amounts of labelled amino acid C in the soils were proportional to their content of silt + clay. After 30 days of incubation labelled amino acid C remaining in the soil with the lowest content of silt + clay constituted 6 per cent of the carbon added in cellulose, as compared with 18 per cent in the soil with the highest content of silt + clay. These values had decreased to 5 and 13 per cent respectively after 2 years of incubation. The order between the soils in the content of labelled amino acid C established during the first month of incubation, was thus roughly maintained throughout the period of incubation. The biological half-life of the labelled C in amino acids varied in the seven soils during the last year of incubation from 3 to 8 years. The variation was, however, not related to the amount of silt + clay.n the soils had been incubated with the labelled material for 2 years, samples of the soils were exposed to “stress” treatments: air drying-rewetting; increased biological activity caused by addition of glucose, and exposure to chloroform vapour. The treatments resulted in an evolution of labelled C in CO, which was 5–10 times larger than the evolution from untreated samples. The increase in the CO₂ evolution caused by the treatments in the different soils was, however, not related to the amount of silt + clay, and a high content of this material did not protect organic material against the effect of the treatments.is concluded that the silt + clay fraction ensures stabilization of amino acid metabolites produced during the period of intense biological activity that follows the addition of decomposable, energy rich material to the soil. The amount of amino acid metabolites stabilized increased with increasing concentration of silt + clay, but the rate of decay of the amino acid material during later stages was largely independent of the concentration of silt + clay.     

Decomposition of straw in soil after stepwise repeated additions

Samples of a sandy soil, which had been incubated for 8 years in the field with [¹⁴C]labelled barley straw, were amended with 1, 2, 3 or 4 successive additions of [¹⁴C]labelled straw, respectively, applied at intervals of 3 months. The decomposition of the straw was studied over a 4-yr period of laboratory incubation, following the first repeated application, by determination of the total amount of labelled C in the soils and labelled C in the soil amino acids. The overall pattern of decomposition was similar whether the soil was amended with one or with several successive applications.Four years after the first repeated addition of labelled straw the soils were subjected to a number of “stress” treatments: addition of unlabelled glucose, air-drying, oven-drying, grinding and fumigation with vapour of chloroform, respectively. The CO₂ that developed during the first 10 days after the treatments, less the evolution from untreated samples, was taken as a measure of the effect of the treatments. The amount of biomass in the soils was calculated from the increase caused by the fumigation with chloroform. In soil incubated undisturbed in the field for 12 yr, biomass accounted for 2.6% of the labelled C in the soil, whereas it was only half this amount in the soil incubated for 8 yr in the field followed by 4 yr in the laboratory. In the soils amended with successive additions of labelled straw, the size of the biomass showed declining values with an increasing number of additions. Biomass thus accounted for 2.6% of the labelled C in the soil amended with one repeated addition, and 1.0% in the soil amended with 4 repeated additions.The increase in the evolution of labelled CO₂-C caused by the stress treatments ranged from 0.3 to 1.7% of the labelled C in the soil: air-drying had the least effect, grinding the most. The effect of each treatment declined with an increasing number of successive additions of straw. The ratio between CO₂ evolved after grinding and fumigation, respectively, revealed that grinding also exposed non-biomass material to accelerated decomposition.The effects of the stress treatments on the evolution of native CO₂-C was on the whole parallel to the effects on the evolution of labelled CO₂-C.     

Does adding microbial mechanisms of decomposition improve soil organic matter models? A comparison of four models using data from a pulsed rewetting experiment

Contemporary soil organic matter (SOM) models have been successful at simulating decomposition across a range of spatial and temporal scales using first-order kinetics to represent the decomposition process; however, recent work suggests the simplicity of the first-order representation of decomposition is not adequate to capture the microbially-driven dynamics of SOM decomposition over short timescales. For example, the response of soils to drying-rewetting events may best be explained by microbial and/or exoenzyme controls on decomposition. To test if adding these microbial mechanisms improves the ability of SOM models to simulate the response of soils to short-term environmental changes, we developed four different SOM decomposition models with varying mechanistic complexity and compared their ability to simulate soil respiration from a pulsed drying-rewetting laboratory-based experiment. Specifically, we tested the ability of the models to capture the timing and magnitude of soil CO₂ efflux in response to rewetting or constant moisture conditions. The results of the comparison suggest that the inclusion of exoenzyme and microbial controls on decomposition can improve the ability to simulate pulsed rewetting dynamics; however, less mechanistic first-order models prevail under steady-state moisture conditions. These modeling results may have implications for understanding the long-term response of soil carbon stocks in response to local and regional climate change.     

Soil CO2 evolution: Response from arginine additions

Short-term response of soil C mineralization following drying/rewetting has been proposed as an indicator of soil microbial activity. Houston Black clay was amended with four rates of arginine to vary microbial responses and keep other soil properties constant. The evolution of CO₂ during 1 and 3 days following rewetting of dried soil was highly related to CO₂ evolution during 10 days following chloroform fumigation (r² = 0.92 and 0.93, respectively) which is a widely used method for soil microbial biomass C, which disrupts cellular membranes. This study suggest that the release of CO₂ following rewetting of dried soil with no amendments other than heat and water can be highly indicative of soil microbial activity and possibly be used as a quantitative measurement of soil biological quality in Houston Black soils.     

Isotopic analysis of respired CO2 during decomposition of separated soil organic matter pools

A detailed understanding of the processes that contribute to the δ¹³C value of respired CO₂ is necessary to make links between the isotopic signature of CO₂ efflux from the soil surface and various sources within the soil profile. We used density fractionation to divide soils from two forested sites that are a part of an ongoing detrital manipulation experiment (the Detrital Input and Removal Treatments, or DIRT project) into two soil organic matter pools, each of which contributes differently to total soil CO₂ efflux. In both sites, distinct biological pools resulted from density fractionation; however, our results do not always support the concept that the light fraction is readily decomposable whereas the heavy fraction is recalcitrant. In a laboratory incubation following density fractionation we found that cumulative respiration over the course of the incubation period was greater from the light fraction than from the heavy fraction for the deciduous site, while the opposite was true for the coniferous site.Use of stable isotopes yielded insight as to the nature of the density fractions, with the heavy fraction solids from both forests isotopically enriched relative to those of the light fraction. The isotopic signature of respired CO₂, however, was more complicated. During incubation of the fractions there was an initial isotopic depletion of the respired CO₂ compared to the substrate for both soil fractions from both forests. Over time for both fractions of both soils the respired δ¹³C reflected more closely the initial substrate value; however, the transition from depleted to enriched respiration relative to substrate occurs at a different stage of decomposition depending on site and substrate recalcitrance. We found a relationship between cumulative respiration during the incubation period and the duration of the transition from isotopically depleted to enriched respiration in the coniferous site but not the deciduous site. Our results suggest that a shift in microbial community or to dead microbial biomass as a substrate could be responsible for the transition in the isotopic signature of respired CO₂ during decomposition. It is likely that a combination of organic matter quality and isotopic discrimination by microbes, in addition to differences in microbial community composition, contribute to the isotopic signature of different organic matter fractions. It is apparent that respired δ¹³CO₂ cannot be assumed to be a direct representation of the substrate δ¹³C. Detailed knowledge of the soil characteristics at a particular site is necessary to interpret relationships between the isotopic values of a substrate and respired CO₂.     

Humic acids as electron acceptors in wetland decomposition

Decomposition of organic matter in inundated wetland soils requires a number of interdependent microbial processes that ultimately generate CO₂ and CH₄. Largely as the result of anaerobic decomposition, wetland soils store globally significant amounts of organic carbon and are currently net sources of CH₄ to the atmosphere. Given the importance of wetlands in the global carbon cycle, it is important to understand controls on anaerobic decomposition in order to predict feedbacks between wetland soils and global climate change. One perplexing pattern observed in many wetland soils is the high proportion of CO₂ resulting from anaerobic decomposition that cannot be explained by any measured pathway of microbial respiration. Recent studies have hypothesized that humic substances, and in particular solid-phase humic substances in wetland soils, can support anaerobic microbial respiration by acting as organic electron acceptors. Humic substances may thus account for much of the currently unexplained CO₂ measured during decomposition in wetland soils. Here we demonstrate that humic acids extracted from a variety of wetland soils act as either electron donors or electron acceptors and alter the ratio of CO₂:CH₄ produced during anaerobic laboratory incubations. Our results suggest that soil-derived humic substances may play an important, and currently unexplored, role in anaerobic decomposition in wetland soils.     

Drying-rewetting events reduce C and N losses from a Norway spruce forest floor

Periods of prolonged summer drought are likely to be expected for this century, with possibly strong effects on carbon (C) and nitrogen (N) mineralization in soils. Drought generally reduces mineralization rates, but the possibility of excess mineralization pulses during rewetting raises the question about the net effect of drying-rewetting events. In this experiment, we measured C and N mineralization in undisturbed soil columns that were either kept under continuously moist conditions (control) or that were subjected to drying-rewetting. We had three treatments (D1-D3) with different drying intensity (increasing from D1 to D3) but uniform rewetting intensity (4 mm d⁻¹). Soil columns were taken from a Norway spruce forest in Bavaria, Germany. The CO₂ fluxes from control and treatment groups were identical before drying. Over the 80 d drought period, total CO₂ emissions from D1, D2, and D3 were only 72, 52 and 43% of that from the control, respectively. Rewetting resulted in a fast increase of CO₂ fluxes to approx. the same level as in the control. Rewetting could not restore soil moisture of the dry soil to the level of the control, presumably because of preferential flow and water repellency of soil organic matter. No significant excess C mineralization during the 40 d rewetting period was observed. Adding up total CO₂ fluxes during drought and rewetting period, the treatments D1, D2, and D3 emitted only 88, 71 and 67% of the CO₂ emitted by the control. Measurements of dissolved organic carbon (DOC) did only show minor differences between control and treatment columns, indicating that no significant accumulation of DOC took place during the drought period. Radiocarbon signature of emitted CO₂ indicated that C mineralization was reduced with decreasing water availability and no new substrate became bioavailable. Net N mineralization over the course of the whole experiment was reduced by drought to 77, 65 or 52% of the control. Net nitrification was virtually zero during drought whereas net ammonification continued at reduced levels. In summary, we found that drying-rewetting generally reduced C and N mineralization in this soil and that the total reduction increased with drought intensity.