Trace gas emissions from soil of the central highlands of Mexico as affected by natural vegetation: a laboratory study

In the central highlands of Mexico, mesquite (Prosopis laevigata) and huisache (Acacia schaffneri), N₂-fixing trees or shrubs, dominate the vegetation and are currently used in a reforestation program to prevent erosion. We investigated how natural vegetation or cultivation of soil affected oxidation of CH₄, and production of N₂O. Soil was sampled under the canopy of mesquite (MES treatment) and huisache trees (HUI treatment), outside their canopy (OUT treatment) and from fields cultivated with maize (ARA treatment) at three different sites while production of CO₂, and dynamics of CH₄, N₂O and inorganic N (NH₄⁺, and NO₃^–) were monitored in an aerobic incubation. The production of CO₂ was 2.3 times higher and significantly greater in the OUT treatment, 3.0 times higher in the MES treatment and 4.0 times higher in the HUI treatment compared to the ARA treatment. There was no significant difference in oxidation of CH₄ between the treatments, which ranged from 0.019 g CH₄–C kg^–1 day^–1 for the HUI treatment to 0.033 CH₄–C kg^–1 day^–1 for the MES treatment. The production of N₂O was 30 g N₂O–N kg^–1 day^–1 in the MES treatment and >8 times higher compared to the other treatments. The average concentration of NO₃^– was 2 times higher and significantly greater in the MES treatment than in the HUI treatment, 3 times greater than in the OUT treatment and 10 times greater than in the ARA treatment. It was found that cultivation of soil decreased soil organic matter content, C and N mineralization, but not oxidation of CH₄ or production of N₂O.     

GREENHOUSE GAS EMISSIONS FROM AN ALKALINE SALINE SOIL CULTIVATED WITH MAIZE (ZEA MAYS L.) AND AMENDED WITH ANAEROBICALLY DIGESTED COW MANURE: A GREENHOUSE EXPERIMENT

Sludge derived from cow manure anaerobically digested to produce biogas (methane; CH₄) was applied to maize (Zea mays L.) cultivated in a nutrient-low, alkaline, saline soil with electrolytic conductivity 9.4 dS m^?1 and pH 9.3. Carbon dioxide (CO₂) emission increased 3.1 times when sludge was applied to soil, 1.6 times when cultivated with maize and 3.5 times in sludge-amended maize cultivated soil compared to the unamended uncultivated soil (1.51 mg C kg^?1 soil day^?1). Nitrous oxide (N₂O) emission from unamended soil was -0.0004 μg nitrogen (N) kg^?1 soil day^?1 and similar from soil cultivated with maize (0.27 μg N kg^?1 soil day^?1). Application of sludge increased the N₂O emission to 4.59 μg N kg^?1 soil day^?1, but cultivating this soil reduced it to 2.42 μg N kg^?1 soil day^?1. It was found that application of anaerobic digested cow manure stimulated maize development in an alkaline saline soil and increased emissions of CO₂ and N₂O.     

Tree species affect atmospheric CH4 oxidation without altering community composition of soil methanotrophs

Plant species exert strong effects on ecosystem functions and one of the emerging, and difficult to test hypotheses, is that plants alter soil functions through changing the community structure of soil microorganisms. We tested the hypothesis for atmospheric CH₄ oxidation by using soil samples from a Siberian afforestation experiment and exposing them to ¹³C-CH₄. We determined the activity of the soil methanotrophs under different tree species at three levels of initial CH₄ concentration (30, 200 and 1000 ppm) thus distinguishing the activities of low- and high-affinity methanotrophs. Half of the samples were incubated with ¹³C-enriched CH₄ (99.9%) and half with ¹²C-CH₄. This allowed an estimation of the amount of ¹³C incorporated into individual PLFAs and determination of PLFAs of methanotrophs involved in CH₄ oxidation at the different CH₄ concentrations. Tree species strongly altered the activity of atmospheric CH₄ oxidation without appearing to change the composition of high-affinity methanotrophs as evidenced by PLFA ¹³C labeling. The low diversity of atmospheric CH₄ oxidizers, presumably belonging to the UCSα group, may explain the lack of tree species effects on the composition of soil methanotrophs. We submit that the observed tree species effects on atmospheric CH₄ oxidation indicate an effect on biomass or cell-specific activities rather than by a community change and this may be related to the impact of the tree species on soil N cycling.     

Varying atmospheric methane concentrations affect soil methane oxidation rates and methanotroph populations in pasture,an adjacent pine forest,and a landfill

We describe experiments to better understand how CH₄ oxidation rates by different methanotroph communities respond to changing CH₄ concentrations. We used a novel system of automatically monitored chambers to investigate the response of CH₄ oxidation rates in a New Zealand pasture and adjacent pine forest soil exposed to varying atmospheric CH₄ concentrations.Type II methanotrophs that dominate CH₄ oxidation in the forest soil became progressively saturated as CH₄ concentrations rose from ambient (1.8 ppmv) to 570 ppmv, as shown by a decrease in uptake efficiency from 20% to 2% removal. By contrast, CH₄ oxidation in the pasture soil where Type I methanotrophs dominate increased in proportion to the increase in CH₄ inlet concentration, oxidising about 2% of the inlet CH₄ flux throughout. Modelling based on Michaelis-Menten kinetics revealed that low-affinity (Type I) methanotrophs were solely responsible for CH₄ oxidation in pasture soils, whereas high affinity (Type II) methanotrophs only contributed about 10% of the CH₄ oxidation in the forest soil. Increased aeration status using a soil–perlite (1:1) mixture doubled CH₄ oxidation rates at both ambient (1.8 ppmv) and 40 ppmv atmospheric CH₄. A similar volcanic soil previously exposed for 8 y to high CH₄ fluxes from a landfill had removal efficiencies consistently above 95% for atmospheric CH₄ concentrations up to 7500 ppmv when the CH₄ oxidation rate was7000 μg CH₄ kg⁻¹soil h⁻¹.     

Short-term effects of nitrogen on methane oxidation in soils

 The short-term effects of N addition on CH₄ oxidation were studied in two soils. Both sites are unfertilized, one has been under long-term arable rotation, the other is a grassland that has been cut for hay for the past 125 years. The sites showed clear differences in their capacity to oxidise CH₄, the arable soil oxidised CH₄ at a rate of 0.013 μg CH₄ kg^–1 h^–1 and the grassland soil approximately an order of magnitude quicker. In both sites the addition of (NH₄)₂SO₄ caused an immediate reduction in the rate of atmospheric CH₄ oxidation approximately in inverse proportion to the amount of NH₄ ⁺ added. The addition of KNO₃ caused no change in the rate of CH₄ oxidation in the arable soil, but in the grassland soil after 9 days the rate of CH₄ oxidation had decreased from 0.22 μg CH₄ kg^–1 h^–1 to 0.13 μg CH₄ kg^–1 h^–1 in soil treated with the equivalent of 192 kg N ha^–1. A ¹⁵N isotopic dilution technique was used to investigate the role of nitrifiers in regulating CH₄ oxidation. The arable soil showed a low rate of gross N mineralisation (0.67 mg N kg^–1 day^–1), but a relatively high proportion of the mineralised N was nitrified. The grassland soil had a high rate of gross N mineralisation (18.28 mg N kg^–1 day^–1), but negligible nitrification activity. It is hypothesised that since there was virtually no nitrification in the grassland soil then CH₄ oxidation at this site must be methanotroph mediated. Received: 31 October 1997     

CH4 oxidation in two temperate arable soils as affected by nitrate and ammonium application

The short-term effect of NaNO₃ or (NH₄)₂SO₄ application on CH₄ oxidation was measured under laboratory conditions with sieved soils collected from the top layer (0–12 cm) of a loamy and a sandy soil. The soils were incubated in sealed flasks and the CH₄ and CO₂ concentrations in headspace were measured periodically. On each gas sampling date the soils were analysed for inorganic N, electro-ultrafiltration organic N, and pH. NH ₄ ⁺ application to the loamy soil inhibited CH₄ oxidation entirely whereas in the untreated control soils CH₄ concentration decreased linearly with a rate of-41 nl CH₄ l^-1 h^-1; NO ₃ ^sup- application to this soil caused a small but significant reduction in CH₄ uptake. The CH₄-oxidizing ability of the sandy soil was low, even in the control. This was mainly a result of the disturbed soil structure after sieving. Both NH ₄ ⁺ and NO ₃ ^sup- treatments completely inhibited CH₄ uptake in this ligh-textured soil. The adverse impact of NH ₄ ⁺ persisted during the entire incubation, although in the loamy soil only 17% of the NH ₄ ⁺ added was recovered after 168 h. The negative effect of NO ₃ ^sup- was probably caused by an increase in osmotic potential. Immediate inhibition of CH₄ oxidation after inorganic N addition was demonstrated in two arable soils, although the effect was directly related only in part to soil N transformations.     

Effect of heavy metals contamination on root-derived and organic matter-derived CO2 efflux from soil planted with Zea mays

The CO₂ efflux from loamy Haplic Luvisol and heavy metal (HM) uptake by Zea mays L. were studied under increased HM contamination: Cd, Cu, and Ni up to 20, 1000, and 2500 mg kg⁻¹ soil, respectively. Split-root system with contrasting HM concentrations in both soil halves was used to investigate root-mediated HM translocation in uncontaminated soil zones. To separate root-derived and soil organic matter (SOM)-derived CO₂ efflux from soil, ¹⁴CO₂ pulse labeling of 15-, 25-, and 35-days-old plants was applied. The CO₂ evolution from the bare soil was 10.6 μg C–CO₂ d⁻¹ g⁻¹ (32 kg C–CO₂ d⁻¹ ha⁻¹) and was not affected by HM (except 2500 mg Ni kg⁻¹). The average CO₂ efflux from the soil with maize was about two times higher and amounted for about 22.0 μg C–CO₂ d⁻¹ g⁻¹. Portion of assimilates respired in the rhizosphere decreased with plant development from 6.0 to 7.0% of assimilated C for 25-days-old Zea mays to 0.4–2.0% for 45-days-old maize. The effect of the HM on root-derived ¹⁴CO₂ efflux increased with rising HM content in the following order: Cd < Cu < Ni. In Cu and Ni contaminated soils, shoot and root dry matter decreased to 70% and to 50% of the uncontaminated control, respectively. Plants contained much more HM in the roots than in the shoots. A split-root system with contrasting HM concentrations allowed to trace transport of mobile forms of HM by roots from contaminated soil half into the uncontaminated soil half. The portion of mobile HM forms in the soil (1 M NH₄NO₃ extract) increased with contamination and amounted to 9–16%, 2–6% and 1.5–3.5% for Cd, Cu, and Ni, respectively. Corresponding values for the easily available HM (1 M NH₄OAc extract) were 22–52%, 1–20% and 5–8.5%. Heavy metal availability for plants decreased in the following order: Cd > Cu ≥ Ni. No increase of HM availability in the soil was found after maize cultivation.     

Methane concentrations and methanotrophic community structure influence the response of soil methane oxidation to nitrogen content in a temperate forest

Methane oxidation in forest soils removes atmospheric CH₄. Many studies have determined methane uptake rates and their controlling variables, yet the microorganisms involved have rarely been assessed simultaneously over the longer term. We measured methane uptake rates and the community structure of methanotrophic bacteria in temperate forest soil (sandy clay loam) on a monthly basis for two years in South Korea. Methane uptake rates at the field site did not show any seasonal patterns, and net uptake occurred throughout both years. In situ uptake rates and uptake potentials determined in the laboratory were 2.92 ± 4.07 mg CH₄ m⁻² day⁻¹ and 51.6 ± 45.8 ng CH₄ g⁻¹ soil day⁻¹, respectively. Contrary to results from other studies, in situ oxidation rates were positively correlated with soil nitrate concentrations. Short-term experimental nitrate addition (0.20-1.95 μg N g⁻¹ soil) significantly stimulated oxidation rates under low methane concentrations (1.7-2.0 ppmv CH₄), but significantly inhibited oxidation under high methane concentrations (300 ppmv CH₄). We analyzed the community structures of methanotrophic bacteria using a DNA-based fingerprinting method (T-RFLP). Type II methanotrophs dominated under low methane concentrations while Type I methanotrophs dominated under high methane concentrations. Nitrogen addition selectively inhibited Type I methanotrophic bacteria. Overall, the results of this study indicate that the effects of inorganic N on methane uptake depend on methane concentrations and that such a response is related to the dissimilar activation or inhibition of different types of methanotrophic bacteria.     

Temporal and spatial patterns of denitrification enzyme activity and nitrous oxide fluxes in three adjacent vegetated riparian buffer zones

The aim of this study was to investigate temporal and spatial patterns of denitrification enzyme activity (DEA) and nitrous oxide (N₂O) fluxes in three adjacent riparian sites (mixed vegetation, forest and grass). The highest DEA was found in the surface (0–30 cm) soil and varied between 0.7±0.1 mg N kg^–1 day^–1 at 5°C and 5.9±0.4 mg N kg^–1 day^–1 at 15°C. There was no significant difference (P >0.05) between the DEA in the uppermost (0–30 cm and 60–90 cm) soil depths under different vegetation covers. In the two deepest (120–150 cm and 180–210 cm) soil depths the DEA varied between 0.0±0.0 mg N kg^–1 day^–1 at 5°C and 4.4±0.9 mg N kg^–1 day^–1 at 15°C and was clearly associated with the accumulation of buried organic carbon (OC). Two threshold values of OC were observed before DEA started to increase significantly, namely 5 and 25 g OC kg^–1 soil at 10–15°C and 5°C, respectively. In the three riparian sites N₂O fluxes varied between a net N₂O uptake of –0.6±0.4 mg N₂O-N m^–2 day^–1 and a net N₂O emission of 2.5±0.3 mg N₂O-N m^–2 day^–1. The observed N₂O emission did not lead to an important pollution swapping (from water pollution to greenhouse gas emission). Especially in the mixed vegetation and forest riparian site highest N₂O fluxes were observed upslope of the riparian site. The N₂O fluxes showed no clear temporal trend.     

Short-term effect of urea on CH4 flux under the oil palm (Elaeis guineensis) on tropical peatland in Sarawak,Malaysia

Abstract

Methane flux was measured monthly from August 2002 to July 2003 at an oil palm plantation on tropical peatland in Sarawak, Malaysia, using a closed chamber technique. Urea was applied twice, once in November 2002 and once in May 2003. The monthly CH₄ flux ranged from ?32.78 to 4.17 µg C m^?2 h^?1. Urea applications increased CH₄ emissions in the month of application and emissions remained slightly higher a month later before the effect disappeared in the third month after application (i.e. back to CH₄ uptake). This effect was the result of increased soil NH⁺ ₄ content that was not immediately absorbed by the oil palm following urea application, which reduced the oxidation of CH₄, resulting in its enhanced emission. By using the Cate–Nelson linear-plateau model, the critical soil NH⁺ ₄ content causing CH₄ emissions in the oil palm ecosystem was 42.75 mg kg^?1 soil. However, the inhibitory effect of NH⁺ ₄ on the oxidation of CH₄ was mitigated by low rainfall and the pyrophosphate solubility index (PSI), where the former might increase oxidation of CH₄ and the latter was a reflection of the low soluble substrate for methane production. Thus, the splitting and timing of urea applications are important not only to optimize oil palm yield, but also to reduce soil NH⁺ ₄ content to minimize CH₄ emissions and, therefore, its potential negative impact on the environment.     

Effect of summer throughfall exclusion, summer drought, and winter snow cover on methane fluxes in a temperate forest soil

Soil moisture strongly controls the uptake of atmospheric methane by limiting the diffusion of methane into the soil, resulting in a negative correlation between soil moisture and methane uptake rates under most non-drought conditions. However, little is known about the effect of water stress on methane uptake in temperate forests during severe droughts. We simulated extreme summer droughts by exclusion of 168 mm (2001) and 344 mm (2002) throughfall using three translucent roofs in a mixed deciduous forest at the Harvard Forest, Massachusetts, USA. The treatment significantly increased CH₄ uptake during the first weeks of throughfall exclusion in 2001 and during most of the 2002 treatment period. Low summertime CH₄ uptake rates were found only briefly in both control and exclusion plots during a natural late summer drought, when water contents below 0.15 g cm⁻³ may have caused water stress of methanotrophs in the A horizon. Because these soils are well drained, the exclusion treatment had little effect on A horizon water content between wetting events, and the effect of water stress was smaller and more brief than was the overall treatment effect on methane diffusion. Methane consumption rates were highest in the A horizon and showed a parabolic relationship between gravimetric water content and CH₄ consumption, with maximum rate at 0.23 g H₂O g⁻¹ soil. On average, about 74% of atmospheric CH₄ was consumed in the top 4-5 cm of the mineral soil. By contrast, little or no CH₄ consumption occurred in the O horizon. Snow cover significantly reduced the uptake rate from December to March. Removal of snow enhanced CH₄ uptake by about 700-1000%, resulting in uptake rates similar to those measured during the growing season. Soil temperatures had little effect on CH₄ uptake as long as the mineral soil was not frozen, indicating strong substrate limitation of methanotrophs throughout the year. Our results suggest that the extension of snow periods may affect the annual rate of CH₄ oxidation and that summer droughts may increase the soil CH₄ sink of temperate forest soils.     

Methane consumption from ambient atmosphere by a Typic Ustochrept soil as influenced by urea and two nitrification inhibitors

The effect of urea and urea mixed with different doses of two nitrification inhibitors, dicyandiamide (DCD) and karanjin [a furanoflavonoid, extracted from seeds of the karanja (Pongamia glabra Vent.) tree], on methane (CH₄) consumption was examined in a Typic Ustochrept (alluvial inceptisol) soil, collected from a field under rice-wheat rotation. The soil, fertilized with urea (100 mg N kg^-1 soil) and urea combined with different doses of the two inhibitors, DCD and karanjin (each added at 5%, 10%, 15%, 20% and 25% of applied N), was incubated at 25°C, at field capacity moisture content for 35 days. The methane consumption rate ranged between 0.2 and 1.7 µg CH₄ kg^-1 soil day^-1 with little temporal variation (CV =10–31%). It was significantly higher in the control (no fertilizer-N) than other treatments except for a few cases, while total CH₄ consumption in the incubation period was significantly higher in the control than other treatments. Methane consumption rate was found to be negatively and positively correlated with soil NH₄ ⁺ and NO₂ ^- + NO₃ ^- content, respectively. Mean CH₄ consumption rate, as well as total CH₄ consumption, was lower on the addition of karanjin due to slower nitrification and higher conservation of NH₄ ⁺ released from applied urea. Addition of urea led to a 17% reduction of total CH₄ consumption while urea combined with karanjin and DCD had 50–64% and 19–34% reduction, respectively. Karanjin was a more effective nitrification inhibitor than DCD during the incubation period.     

Influence of oxygen on denitrification and aerobic respiration in soil

Summary The influence of the partial pressure of oxygen on denitrification and aerobic respiration was investigated at defined P02 values in a mull rendzina soil. The highest denitrification and respiration rates obtained in remoistened, glucose- and nitrate-amended soil were 43 1 N₂0 h^–1g^–1 soil and 130 1 O₂ h^–1g^–1 soil, respectively. At -55 kPa matric water potential, corresponding to 40% water saturation, N₂0 was produced only below P0₂ 40 hPa. The K _m, for O₂ was 3.0 x 10^–6 M. Formation of N₂O and consumption of O₂ occurred simultaneously with half maximum rates at P0₂ 6.7–13.3 hPa. Nitrite accumulated in soil below 40 hPa and increased with decreasing pO₂. The upper threshold for N₂0 formation in amended soil was P0₂ 33–40 hPa (39-47 M O₂).     

中国亚热带中部三峡库区不同土地利用方式下甲烷氧化潜力研究

To compare the CH4 oxidation potential among diferent land uses and seasons,and to observe its response to monsoon precipitation pattern and carbon and nitrogen parameters,a one-year study was conducted for diferent land uses (vegetable field,tilled and non-tilled orchard,upland crops and pine forest) in central subtropical China.Results showed significant diferences in CH4 oxidation potential among diferent land uses(ranging from 3.08 to 0.36 kg CH4 ha-1 year-1).Upland with corn-peanut-sweet potato rotation showed the highest CH4 emission,while pine forest showed the highest CH4 oxidation potential among all land uses.Non-tilled citrus orchard (0.72±0.08 kg CH4 ha-1 year-1)absorbed two times more CH4 than tilled citrus orchard(0.38±0.06kg CH4 ha-1 year-1).Irrespective of diferent vegetation,inorganic N fertilizer application significantly influenced CH4 fluxes across the sites (R2=0.86,P=0.002).Water-filled pore space,soil microbial biomass carbon,and dissolved nitrogen showed significant efects across diferent land uses (31% to 38% of variability)in one linear regression model.However,their cumulative interaction was significant for pine forest only,which might be attributed to undisturbed microbial communities legitimately responding to other variables,leading to net CH4 oxidation in the soil.These results suggested that i)natural soil condition tended to create win-win situation for CH4 oxidation,and agricultural activities could disrupt the oxidation potentials of the soils;and ii)specific management practices including but not limiting to efficient fertilizer application and utilization,water use efciency,and less soil disruption might be required to increase the CH4 uptake from the soil.     

Labile carbon and methane uptake as affected by tillage intensity in a Mollisol

Methane (CH₄) oxidation potential of soils decreases with cultivation, but limited information is available regarding the restoration of that capacity with implementation of reduced tillage practices. A study was conducted to assess the impact of tillage intensity on CH₄ oxidation and several C-cycling indices including total and active microbial biomass C (t-MBC, a-MBC), mineralizable C (C_min) and N (N_min), and aggregate-protected C. Intact cores and disturbed soil samples (0–5 and 5–15 cm) were collected from a corn (Zea mays L.)–soybean (Glycine max L. Merr.) rotation under moldboard-plow (MP), chisel-plow (CP) and no-till (NT) for 8 years. An adjacent pasture (<25 years) and secondary growth forest (>60 years) soils were also sampled as references. At all sites, soil was a Kokomo silty clay loam (mesic Typic Argiaquolls). Significant tillage effects on t-MBC and protected C were found in the 0–5 cm depth. Protected C, a measure of C retained within macro-aggregates and defined as the difference in C_min (CO₂ evolved in a 56 days incubation) between intact and sieved (<2 mm) soil samples, amounted to 516, 162 and 121 mg C kg⁻¹ soil in the 0–5 cm layer of the forest, pasture and NT soils, respectively. Protected C was negligible in the CP and MP soils. Methane uptake rate (μg CH₄-C kg⁻¹ soil per day, under ambient CH₄) was higher in forest (2.70) than in pasture (1.22) and cropland (0.61) soils. No significant tillage effect on CH₄ oxidation rate was detected (MP: 0.82; CP: 0.41; NT: 0.61). These results underscore the slow recovery of the CH₄ uptake capacity of soils and suggest that, to have an impact, tillage reduction may need to be implemented for several decades.     

Response of CH<Subscript>4</Subscript> oxidation and methanotrophic diversity to NH<Subscript>4</Subscript><Superscript>+</Superscript> and CH<Subscript>4</Subscript> mixing ratios

Methane oxidising activity and community structure of 11, specifically targeted, methanotrophic species have been examined in an arable soil. Soils were sampled from three different field plots, receiving no fertilisation (C), compost (G) and mineral fertiliser (M), respectively. Incubation experiments were carried out with and without pre-incubation at elevated CH₄ mixing ratios (100 ml CH₄ l⁻¹) and with and without ammonium (100 mg N kg⁻¹) pre-incubation. Four months after fertilisation, plots C, G and M did not show significant differences in physicochemical properties and CH₄ oxidising activity. The total number of methanotrophs (determined as the sum the 11 specifically targeted methanotrophs) in the fresh soils was 17.0×10⁶, 13.7×10⁶ and 15.5×10⁶ cells g⁻¹ for treatment C, G and M, respectively. This corresponded to 0.11 to 0.32% of the total bacterial number. The CH₄ oxidising activity increased 10⁵-fold (20–26 mg CH₄ g⁻¹ h⁻¹), the total number of methanotrophs doubled (28–76×10⁶ cells g⁻¹) and the methanotrophic diversity markedly increased in treatments with a pre-incubation at elevated CH₄ concentrations. In all soils and treatments, type II methanotrophs (62–91%) outnumbered type I methanotrophs (9–38%). Methylocystis and Methylosinus species were always most abundant. After pre-incubation with ammonium, CH₄ oxidation was completely inhibited; however, no change in the methanotrophic community structure could be detected.     

Influence of extractable iron,aluminium, and manganese on P-sorption in flooded acid sulfate soils

We evaluated the effect of 1 N NH₄OAc and sodium-citrate dithionite extractable forms of soil Fe, Al, and Mn on P-sorption of a flooded acid sulfate soil (Sulfic Tropaquepts) and a non-acid sulfate soil (Typic Tropaquepts) under different soil oxidation-reduction and pH conditions. We used Maha-Phot soil (Sulfic Tropaquepts) and Bangkok soil (Typic Tropaquepts) from the Bangkok Plain, Thailand, and incubated them with 0.2% rice straw under aerobic (O₂ atmosphere) and anaerobic (N₂ atmosphere) conditions at three different levels of pH (4.0, 5.0, and 6.0) for 6 weeks in stirred soil suspensions with a soil to 0.01 M CaCl₂ solution ratio of 1:7. After the incubation period, the soil suspensions in the first treatment (control) were not washed or pretreated with any extractants. For the second treatment (II), the soil suspensions were treated with 1 N NH₄OAc (buffered to pH 4.0) to remove Fe, Al, and Mn in exchangeable form. In the third treatment (III), the soils suspensions were treated with sodium citrate dithionite solution (20%) to remove Fe, Al, and Mn in the form of free oxides. The soil residues were then equilibrated with KH₂PO₄ ranging from 0 to 500 mg P kg^-1 soil. Sorption isotherms were described by the classical Langmuir equation. The P-sorption parameters under study were standard P requirement (SPR), Langmuir maximum sorption capacity (X _m), Langmuir sorption constant (k), and buffering index (BI). Treating soils with 1 N NH₄OAc reduced X _m by 32–55%, SPR by 68–84%, and also decreased the differences in P-sorption due to the effects of pH and oxidation-reduction conditions. Significant correlations between the P-sorption parameters and the amount of free iron oxides indicated the primary role of iron oxides in P-sorption of acid sulfate soils. Aluminium oxides seemed to play a secondary role in P-sorption of these soils. Manganese also showed an important effect on P-sorption, but the mechanism is ambiguous.This is a contribution from the Wetland Biogeochemistry Institute, Louisiana State University, Baton Rouge, LA 70803-7511     

Increased moisture and methanogenesis contribute to reduced methane oxidation in elevated CO2 soils

Awareness of global warming has stimulated research on environmental controls of soil methane (CH₄) consumption and the effects of increasing atmospheric carbon dioxide (CO₂) on the terrestrial CH₄ sink. In this study, factors impacting soil CH₄ consumption were investigated using laboratory incubations of soils collected at the Free Air Carbon Transfer and Storage I site in the Duke Forest, NC, where plots have been exposed to ambient (370 μL L⁻¹) or elevated (ambient + 200 μL L⁻¹) CO₂ since August 1996. Over 1 year, nearly 90% of the 360 incubations showed net CH₄ consumption, confirming that CH₄-oxidizing (methanotrophic) bacteria were active. Soil moisture was significantly (p < 0.01) higher in the 25–30 cm layer of elevated CO₂ soils over the length of the study, but soil moisture was equal between CO₂ treatments in shallower soils. The increased soil moisture corresponded to decreased net CH₄ oxidation, as elevated CO₂ soils also oxidized 70% less CH₄ at the 25–30 cm depth compared to ambient CO₂ soils, while CH₄ consumption was equal between treatments in shallower soils. Soil moisture content predicted (p < 0.05) CH₄ consumption in upper layers of ambient CO₂ soils, but this relationship was not significant in elevated CO₂ soils at any depth, suggesting that environmental factors in addition to moisture were influencing net CH₄ oxidation under elevated CO₂. More than 6% of the activity assays showed net CH₄ production, and of these, 80% contained soils from elevated CO₂ plots. In addition, more than 50% of the CH₄-producing flasks from elevated CO₂ sites contained deeper (25–30 cm) soils. These results indicate that subsurface (25 cm+) CH₄ production contributes to decreased net CH₄ consumption under elevated CO₂ in otherwise aerobic soils.     

CO2 efflux by rapid decomposition of low molecular organic substances in soils

Decomposition rates of the [2-¹⁴C]-glucose and [2-¹⁴C]-glycine in four different soils of the long-term field trial of Moscow were investigated in a 3-months laboratory experiment in which ¹⁴CO₂ respiration was measured. A model with three decomposition components and two distribution parameters was developed and validated with the data of the experiment. The decay rate constants of free [2-¹⁴C]-glucose (4–32 day^-1) were slower than those of [2-¹⁴C]-glycine (16–44 day^-1). The calculated use efficiency for microbial biosynthesis of the second carbon atom was 47% for glucose and 31% for glycine. The potential half-life of labelled carbon in the microbial soil biomass ranged from 0.6 to 4.4 days, depending on the soil type and the initial amount of added substrate. The calculated total utilisation of carbon by the soil biomass from glycine was about 2–5 times lower than that of glucose.The modelled ¹⁴C incorporation into the microbial soil biomass reached its maximum on the first day of the incubation experiment and did not exceed 22% of the ¹⁴C input. Both of the investigated substances decomposed most rapidly in the soil samples from sites that have not being fertilised with organic or mineral fertilisers during an 81-years period.     

Growth rates,establishment, and effects on herbage yield of introduced earthworms in grassland on reclaimed cutover peat

Summary Lumbricus terrestris L. juveniles confined in nylon mesh bags grew at mean rates of 6–12 mg ind^–1 day^–1 in reclaimed peat grassland soil, while the growth rates of Aporrectodea caliginosa (Sav.) juveniles were 1.5–2.1 mg ind^–1 day^–1. Earthworm population densities exceeding 700 m² had become established within 1 year adjacent to sods transplanted from an old pasture, while microplots enclosed in nylon mesh cages had mean population densities of 318–408 earthworms m^–2 and biomass of 89–111 g m^–2 3–4 1/2 years after inoculation. Herbage yields were 25% greater in the 2nd year and 49% greater in the 3rd year in earthworm-inoculated microplots which received an annual application of cattle slurry compared with similarly fertilized, non-inoculated cages.Dedicated to the late Prof. Dr. M.S. Ghilarov