Heterotrophic Soil Respiration in Relation to Environmental Factors and Microbial Biomass in Two Wet Tropical Forests

We examined the correlation between fungal and bacterial biomass, abiotic factors such as soil moisture, carbon in the light soil fraction and soil nitrogen to a depth of 0–25 cm and heterotrophic soil respiration using a trenching technique – in a secondary forest (Myrcia splendens, Miconia prasina and Casearia arborea) and a pine (Pinus caribeae) plantation in the Luquillo Experimental Forest in Puerto Rico. Soil respiration was significantly reduced where roots were excluded for 7 years in both the secondary forest and the pine plantation. Microbial biomass was also significantly reduced in the root exclusion plots. In root exclusion treatment, total fungal biomass was on average 31 and 65% lower than the control plots in the pine plantation and the secondary forest, respectively, but the total bacterial biomass was 24 and 8.3% lower than the control plots in the pine plantation and the secondary forest, respectively. Heterotrophic soil respiration was positively correlated with fungal biomass (R²=0.63, R²=0.39), bacterial biomass (R²=0.16, R²=0.45), soil moisture (R²=0.41, R²=0.56), carbon in light fraction (R²=0.45, R²=0.39) and total nitrogen (R²=0.69, R²=0.67) in the pine plantation and the secondary forest, respectively. The regression analysis suggested that fungal biomass might have a greater influence on heterotrophic soil respiration in the pine plantation, while the bacterial biomass might have a greater influence in the secondary forest. Heterotrophic soil respiration was more sensitive to total N than to carbon in the light fraction, and soil moisture was a major factor influencing heterotrophic soil respiration in these forests where temperature is high and relatively invariable.     

Contribution of aboveground litter,belowground litter,and rhizosphere respiration to total soil CO<Subscript>2</Subscript> efflux in an old growth coniferous forest

In an old growth coniferous forest located in the central Cascade Mountains, Oregon, we added or removed aboveground litter and terminated live root activity by trenching to determine sources of soil respiration. Annual soil efflux from control plots ranged from 727 g C m⁻² year⁻¹ in 2002 to 841 g C m⁻² year⁻¹ in 2003. We used aboveground litter inputs (149.6 g C m⁻² year⁻¹) and differences in soil CO₂ effluxes among treatment plots to calculate contributions to total soil efflux by roots and associated rhizosphere organisms and by heterotrophic decomposition of organic matter derived from aboveground and belowground litter. On average, root and rhizospheric respiration (R_r) contributed 23%, aboveground litter decomposition contributed 19%, and belowground litter decomposition contributed 58% to total soil CO₂ efflux, respectively. These values fall within the range of values reported elsewhere, although our estimate of belowground litter contribution is higher than many published estimates, which we argue is a reflection of the high degree of mycorrhizal association and low nutrient status of this ecosystem. Additionally, we found that measured fluxes from plots with doubled needle litter led to an additional 186 g C m⁻² year⁻¹ beyond that expected based on the amount of additional carbon added; this represents a priming effect of 187%, or a 34% increase in the total carbon flux from the plots. This finding has strong implications for soil C storage, showing that it is inaccurate to assume that increases in net primary productivity will translate simply and directly into additional belowground storage.     

Temporal variation in CO<Subscript>2</Subscript> efflux from soil and snow surfaces in a Japanese cedar (<Emphasis Type="Italic">Cryptomeria japonica</Emphasis>) plantation,central Japan

CO₂ efflux from soil and snow surfaces was measured continuously in a Japanese cedar (Cryptomeria japonica D. Don) forest in central Japan using an open dynamic chamber system. The chamber opens and closes automatically and records measurements based on an open-flow dynamic method. Between May and December, mean soil CO₂ efflux ranged from 1,529 mg CO₂ m⁻² h⁻¹ in September to 255 mg CO₂ m⁻² h⁻¹ in December. The seasonal change in CO₂ efflux from the soil paralleled the seasonal pattern of soil temperature. No marked diurnal trends in soil CO₂ efflux were observed on days without rainfall, whereas significant pulses in soil CO₂ efflux were observed on days with rainfall. In this plantation, soil CO₂ efflux frequently responded to rainfall. Measurements of changes from litter-covered soil to snow-covered surfaces revealed that CO₂ efflux decreased from values of ca. 250 mg CO₂ m⁻² h⁻¹ above soil to less than 33 mg CO₂ m⁻² h⁻¹ above snow. Soil temperature alone explained 66% of the overall variation in soil CO₂ efflux, but explained approximately 85% of the variation when data from two anomalous periods were excluded. Moreover, we found a significant correlation between soil CO₂ efflux and soil moisture (which explained 44% of the overall variation) using a second-order polynomial function. Our results suggest that the seasonality of CO₂ efflux is affected not only by soil temperature and moisture, but also by drying and rewetting cycles and by litterfall pulses.     

Soil‐surface CO2 efflux and its spatial and temporal variations in a young ponderosa pine plantation in northern California

Soil‐surface CO₂ efflux and its spatial and temporal variations were examined in an 8‐y‐old ponderosa pine plantation in the Sierra Nevada Mountains in California from June 1998 to August 1999. Continuous measurements of soil CO₂ efflux, soil temperatures and moisture were conducted on two 20 × 20 m sampling plots. Microbial biomass, fine root biomass, and the physical and chemical properties of the soil were also measured at each of the 18 sampling locations on the plots. It was found that the mean soil CO₂ efflux in the plantation was 4.43 µmol m^?2 s^?1 in the growing season and 3.12 µmol m^?2 s^?1 in the nongrowing season. These values are in the upper part of the range of published soil‐surface CO₂ efflux data. The annual maximum and minimum CO₂ efflux were 5.87 and 1.67 µmol m^?2 s^?1, respectively, with the maximum occurring between the end of May and early June and the minimum in December. The diurnal fluctuation of CO₂ efflux was relatively small (< 20%) with the minimum appearing around 09.00 hours and the maximum around 14.00 hours. Using daytime measurements of soil CO₂ efflux tends to overestimate the daily mean soil CO₂ efflux by 4–6%. The measurements taken between 09.00 and 11.00 hours (local time) seem to better represent the daily mean with a reduced sampling error of 0.9–1.5%. The spatial variation of soil CO₂ efflux among the 18 sampling points was high, with a coefficient of variation of approximately 30%. Most (84%) of the spatial variation was explained by fine root biomass, microbial biomass, and soil physical and chemical properties. Although soil temperature and moisture explained most of the temporal variations (76–95%) of soil CO₂ efflux, the two variables together explained less than 34% of the spatial variation. Microbial biomass, fine root biomass, soil nitrogen content, organic matter content, and magnesium content were significantly and positively correlated with soil CO₂ efflux, whereas bulk density and pH value were negatively correlated with CO₂ efflux. The relationship between soil CO₂ efflux and soil temperature was significantly controlled by soil moisture with a Q₁₀ value of 1.4 when soil moisture was <14% and 1.8 when soil moisture was >14%. Understanding the spatial and temporal variations is essential to accurately assessment of carbon budget at whole ecosystem and landscape scales. Thus, this study bears important implications for the study of large‐scale ecosystem dynamics, particularly in response to climatic variations and management regimes.     

Accelerated soil CO<Subscript>2</Subscript> efflux after conversion from secondary oak forest to pine plantation in southeastern China

Soil respiration (R _s) is an important component of the carbon cycle in terrestrial ecosystems, and changes in soil respiration with land cover alteration can have important implications for regional carbon balances. In southeastern China (Xiashu Experimental Forest, Jiangsu Province), we used an automated LI-8100 soil CO₂ flux system to quantify diurnal variation of soil respiration in a secondary oak forest and a pine plantation. We found that soil respiration in the pine plantation was significantly higher than that in the secondary oak forest. There were similar patterns of soil respiration throughout the day in both the secondary oak forest and the pine plantation during our 7-month study (March–September 2005). The maximum of R _s occurred between 4:00 pm and 7:00 pm. The diurnal variations of R _s were usually out of phase with soil surface (0.5 cm) temperature (T _g). However, annual variation in R _s correlated with surface soil temperature. Soil respiration reached to a maximum in June, and decreased thereafter. The Q₁₀ of R _s in the secondary oak forest was significantly higher than that in the pine plantation. The higher Q₁₀ value in the secondary oak forest implied that it might release more CO₂ than the pine plantation under a global-warming scenario. Our results indicated that land-use change from secondary forest to plantation may cause a significant increase in CO₂ emission, and reduce the temperature sensitivity of soil respiration in southeastern China.     

Effect of clear-cutting on soil CO<Subscript>2</Subscript> emission

An experimental study to estimate the effect of clear-cutting on CO₂ emission from the soil surface was performed using the chamber method. For field measurements, several experimental plots within the clear-cut with different degrees of damage of the upper organic soil layer and different amounts of litter and logging residue on the surface were selected. Soil CO₂ fluxes were simultaneously measured both on the clear-cutting plots and on two plots within the spruce forest stand located close to the clear-cut area. The results show a significant seasonal and diurnal variability of soil CO₂ emission. It was found that the soil respiration rate varies significantly among plots and depends on the damage to the upper soil layer and the availability of litter and logging residue on the soil surface. It was found that the rate of CO₂ emission from soil surface is strongly dependent on the air and soil temperature and moisture of the upper soil layer. Different rates of soil respiration are also revealed on the plots located at different distances from tree trunks within the control forest stand.     

Effects of Fertilization on Soil CO₂ Efflux in Chinese Hickory (<i>Carya cathayensis</i>) Stand

Chinese hickory (Carya cathayensis Sarg.) is a popular nut tree in China, but there is little information about the influences of fertilization on soil CO₂ efflux and soil microbial biomass. This study evaluated the short-term effects of different fertilizer applications on soil CO₂ efflux and soil microbial biomass in Chinese hickory stands. Four fertilizer treatments were established: control (CK, no fertilizer), inorganic fertilizer (IF), organic fertilizer (OF), and equal parts organic and inorganic N fertilizers (OIF). A field experiment was conducted to measure soil CO₂ effluxes using closed chamber and gas chromatography techniques. Regardless of the fertilization practices, soil CO₂ effluxes of all the treatments showed a similar temporal pattern, with the highest value in summer and the lowest in winter. The mean annual soil CO₂ efflux in the IF treatment was significantly higher than that in the CK, OIF, and OF treatments. There was no significant difference in soil CO₂ efflux between the OIF, OF, and CK treatments. Soil CO₂ effluxes were significantly affected by soil temperature. Soil dissolved organic carbon (DOC) was positively correlated with soil CO₂ efflux only in the CK treatment. Regression analysis, including soil temperature, moisture, and DOC, showed that soil temperature was the primary factor influencing soil CO₂ effluxes. Both OF and OIF treatments increased concentrations of soil microbial biomass carbon (MBC) and microbial biomass nitrogen (MBN), but decreased the ratio of MBC:MBN. These results reveal that applying organic fertilizer, either alone or combined with inorganic fertilizer, may be the optimal strategy for mitigating soil CO₂ emission and improving soil quality in Chinese hickory stands.     

Hydrogen sulfide mediates ion fluxes inducing stomatal closure in response to drought stress in <Emphasis Type="Italic">Arabidopsis thaliana</Emphasis>

Background and aims

Changes in net primary productivity in response to climate change are likely to affect litter inputs to forest soil. However, feedbacks between changes in litter input and soil carbon dynamics remain poorly understood in tropical and subtropical forests. This study aims to test whether the effects of litter manipulation on soil respiration differ between natural and plantation forests.

Methods

Soil respiration, soil properties, fine root biomass and enzyme activity were measured in adjacent plots with doubling vs. eliminating litter input in both natural and plantation forests of Castanopsis carlesii in southern China.

Results

After only 3 years of litter manipulation, the magnitude of change in soil respiration was greater in response to a doubling of the litter input (+24%) than to the elimination of litter input (?15%) in the natural forest, possibly due to a positive priming effect on decomposition of soil organic carbon (SOC). The quick and intense priming effect was corroborated by elevated enzyme activities for five of the six enzymes analyzed. In contrast, the response to litter removal (?31%) was greater than the response to litter addition (1%; not significant) in the plantation forest. The lack of positive priming in the plantation forest may be related to its lower soil fertility, which could not meet the demand of soil microbes, and to its high clay content, which protected SOC from microbial attack. The positive priming effect in the natural forest but not plantation forest of C. carlesii is also consistent with the significant declines in total soil carbon observed following litter addition in the natural forest but not the plantation forest.

Conclusions

Increases in aboveground litter production may trigger priming effects and subsequently transfer more soil carbon to atmospheric CO₂ in the natural forest but not in the plantation forest with low fertility. Changes in litter inputs resulting from global change drivers may have different impacts on natural and plantation forests.

     

Simulated chronic NO3− deposition reduces soil respiration in northern hardwood forests

Chronic N additions to forest ecosystems can enhance soil N availability, potentially leading to reduced C allocation to root systems. This in turn could decrease soil CO₂ efflux. We measured soil respiration during the first, fifth, sixth and eighth years of simulated atmospheric NO₃^? deposition (3 g N m^?2 yr^?1) to four sugar maple‐dominated northern hardwood forests in Michigan to assess these possibilities. During the first year, soil respiration rates were slightly, but not significantly, higher in the NO₃^?‐amended plots. In all subsequent measurement years, soil respiration rates from NO₃^?‐amended soils were significantly depressed. Soil temperature and soil matric potential were measured concurrently with soil respiration and used to develop regression relationships for predicting soil respiration rates. Estimates of growing season and annual soil CO₂ efflux made using these relationships indicate that these C fluxes were depressed by 15% in the eighth year of chronic NO₃^? additions. The decrease in soil respiration was not due to reduced C allocation to roots, as root respiration rates, root biomass, and root turnover were not significantly affected by N additions. Aboveground litter also was unchanged by the 8 years of treatment. Of the remaining potential causes for the decline in soil CO₂ efflux, reduced microbial respiration appears to be the most likely possibility. Documented reductions in microbial biomass and the activities of extracellular enzymes used for litter degradation on the NO₃^?‐amended plots are consistent with this explanation.     

Fine root chemistry and decomposition in model communities of north-temperate tree species show little response to elevated atmospheric CO<Subscript>2</Subscript> and varying soil resource availability

Rising atmospheric [CO₂] has the potential to alter soil carbon (C) cycling by increasing the content of recalcitrant constituents in plant litter, thereby decreasing rates of decomposition. Because fine root turnover constitutes a large fraction of annual NPP, changes in fine root decomposition are especially important. These responses will likely be affected by soil resource availability and the life history characteristics of the dominant tree species. We evaluated the effects of elevated atmospheric [CO₂] and soil resource availability on the production and chemistry, mycorrhizal colonization, and decomposition of fine roots in an early- and late-successional tree species that are economically and ecologically important in north temperate forests. Open-top chambers were used to expose young trembling aspen (Populus tremuloides) and sugar maple (Acer saccharum) trees to ambient (36 Pa) and elevated (56 Pa) atmospheric CO₂. Soil resource availability was composed of two treatments that bracketed the range found in the Upper Lake States, USA. After 2.5 years of growth, sugar maple had greater fine root standing crop due to relatively greater allocation to fine roots (30% of total root biomass) relative to aspen (7% total root biomass). Relative to the low soil resources treatment, aspen fine root biomass increased 76% with increased soil resource availability, but only under elevated [CO₂]. Sugar maple fine root biomass increased 26% with increased soil resource availability (relative to the low soil resources treatment), and showed little response to elevated [CO₂]. Concentrations of N and soluble phenolics, and C/N ratio in roots were similar for the two species, but aspen had slightly higher lignin and lower condensed tannins contents compared to sugar maple. As predicted by source-sink models of carbon allocation, pooled constituents (C/N ratio, soluble phenolics) increased in response to increased relative carbon availability (elevated [CO₂]/low soil resource availability), however, biosynthetically distinct compounds (lignin, starch, condensed tannins) did not always respond as predicted. We found that mycorrhizal colonization of fine roots was not strongly affected by atmospheric [CO₂] or soil resource availability, as indicated by root ergosterol contents. Overall, absolute changes in root chemical composition in response to increases in C and soil resource availability were small and had no effect on soil fungal biomass or specific rates of fine root decomposition. We conclude that root contributions to soil carbon cycling will mainly be influenced by fine root production and turnover responses to rising atmospheric [CO₂], rather than changes in substrate chemistry.     

The effects of elevated atmospheric CO<Subscript>2</Subscript> and nitrogen amendments on subsurface CO<Subscript>2</Subscript> production and concentration dynamics in a maturing pine forest

Profiles of subsurface soil CO₂ concentration, soil temperature, and soil moisture, and throughfall were measured continuously during the years 2005 and 2006 in 16 locations at the free air CO₂ enrichment facility situated within a temperate loblolly pine (Pinus taeda L.) stand. Sampling at these locations followed a 4 by 4 replicated experimental design comprised of two atmospheric CO₂ concentration levels (ambient [CO₂]^a, ambient + 200 ppmv, [CO₂]^e) and two soil nitrogen (N) deposition levels (ambient, ambient + fertilization at 11.2 g_N m⁻² year⁻¹). The combination of these measurements permitted indirect estimation of belowground CO₂ production and flux profiles in the mineral soil. Adjacent to the soil CO₂ profiles, direct (chamber-based) measurements of CO₂ fluxes from the soil–litter complex were simultaneously conducted using the automated carbon efflux system. Based on the measured soil CO₂ profiles, neither [CO₂]^e nor N fertilization had a statistically significant effect on seasonal soil CO₂, CO₂ production, and effluxes from the mineral soil over the study period. Soil moisture and temperature had different effects on CO₂ concentration depending on the depth. Variations in CO₂ were mostly explained by soil temperature at deeper soil layers, while water content was an important driver at the surface (within the first 10 cm), where CO₂ pulses were induced by rainfall events. The soil effluxes were equal to the CO₂ production for most of the time, suggesting that the site reached near steady-state conditions. The fluxes estimated from the CO₂ profiles were highly correlated to the direct measurements when the soil was neither very dry nor very wet. This suggests that a better parameterization of the soil CO₂ diffusivity is required for these soil moisture extremes.     

Feedback interactions between needle litter decomposition and rhizosphere activity

The aim of our study was to identify interactions between the decomposition of aboveground litter and rhizosphere activity. The experimental approach combined the placement of labelled litter (¹³C=–37.9) with forest girdling in a 35-year-old Norway spruce stand, resulting in four different treatment combinations: GL (girdled, litter), GNL (girdled, no litter), NGL (not girdled, litter), and NGNL (not girdled, no litter). Monthly sampling of soil CO₂ efflux and ¹³C of soil respired CO₂ between May and October 2002 allowed the partitioning of the flux into that derived from the labelled litter, and that derived from native soil organic matter and roots. The effect of forest girdling on soil CO₂ efflux was detectable from June (girdling took place in April), and resulted in GNL fluxes to be about 50% of NGNL fluxes by late August. The presence of litter resulted in significantly increased fluxes for the first 2 months of the experiment, with significantly greater litter derived fluxes from non-girdled plots and a significant interaction between girdling and litter treatments over the same period. For NGL collars, the additional efflux was found to originate only in part from litter decomposition, but also from the decay of native soil organic matter. In GL collars, this priming effect was not significant, indicating an active role of the rhizosphere in soil priming. The results therefore indicate mutual positive feedbacks between litter decomposition and rhizosphere activity. Soil biological analysis (microbial and fungal biomass) of the organic layers indicated greatest activity below NGL collars, and we suppose that this increase indicates the mechanism of mutual positive feedback between rhizosphere activity and litter decomposition. However, elimination of fresh C input from both above- and belowground (GNL) also resulted in greater fungal abundance than for the NGNL treatment, indicating likely changes in fungal community structure (i.e. a shift from symbiotic to saprotrophic species abundance).     

An estimation of CO<Subscript>2</Subscript> fixation capacity in mangrove forest using two methods of CO<Subscript>2</Subscript> gas exchange and growth curve analysis

In many coastal areas of South-East Asia, attempts have been made to revive coastal ecosystem by initiating projects that encourage planting of mangrove trees. Compared to the terrestrial trees, mangrove trees possess a higher carbon fixation capacity. It becomes a very significant option for clean development mechanism (CDM) program. However, a reliable method to estimate CO₂ fixation capacity of mangrove trees has not been established. Acknowledging the above fact, we decided to set up an estimation method for the CDM program, using gas exchange analysis to estimate mangrove productivity, we put into consideration the net CO₂ fixation of reforested Kandelia candel (5-, 10-, and 15-year-old stand). This was estimated by gas exchange analysis and growth curve analysis. In growth curve analysis, we drew a growth curve of a single stand using data of above- and below-ground biomass. In the gas exchange analysis, we calculated CO₂ fixation capacity by (1) measuring respiration rate of each organ of stand and calculating respiratory CO₂ emission from above- to below-ground biomass. (2) Measuring the single-leaf photosynthetic rate in response to light intensity and calculating the photosynthetic CO₂ absorption. (3) We also developed a model for the diurnal changes in temperature, and monthly averages based on one-day estimation of CO₂ absorption and emission, which we corrected by this model in order to estimate the net CO₂ fixation capacity in response to temperature. Comparing the biomass accumulation of the two methods constructed for the same forest, the above-ground biomass accumulation of 10-year-old forest (34.3 ton ha⁻¹ yr⁻¹) estimated by gas exchange analysis was closely compared to those of growth curve analysis (26.6 ton ha⁻¹ yr⁻¹), suggesting that the gas exchange analysis was capable of estimating mangrove productivity. The validity of the estimated CO₂ fixation capacity by the gas exchange analysis and the growth curve analysis was also discussed.     

Above- and belowground organic matter storage and production in a tropical pine plantation and a paired broadleaf secondary forest

The distribution of tree biomass and the allocation of organic matter production were measured in an 11-yr-old Pinus caribaea plantation and a paired broadleaf secondary forest growing under the same climatic conditions. The pine plantation had significantly more mass aboveground than the secondary forest (94.9 vs 35.6 t ha^-1 for biomass and 10.5 vs 5.0 t ha^{-1 for litter}), whereas the secondary forest had significantly more fine roots (⩽2 mm diameter) than the pine plantation (10.5 and 1.0 t ha^-1, respectively). Standing stock of dead fine roots was higher than aboveground litter in the secondary forest. In contrast, aboveground litter in pine was more than ten times higher than the dead root fraction. Both pine and secondary forests had similar total organic matter productions (19.2 and 19.4 t ha^-1 yr^-1, respectively) but structural allocation of that production was significantly different between the two forests; 44% of total production was allocated belowground in the secondary forest, whereas 94% was allocated aboveground in pine. The growth strategies represented by fast growth and large structural allocation aboveground, as for pine, and almost half the production allocated belowground, as for the secondary forest, illustrate equally successful, but contrasting growth strategies under the same climate, regardless of soil characteristics. The patterns of accumulation of organic matter in the soil profile indicated contrasting nutrient immobilization and mineralization sites and sources for soil organic matter formation.     

改变凋落物输入对川西亚高山天然次生林土壤呼吸的影响

2019年5月-10月,采用LI-8100A土壤碳通量自动测量分析仪对川西米亚罗林区20世纪60年代采伐后经自然更新恢复形成的岷江冷杉（Abies faxoniana）次生针叶林（针叶林）、红桦（Betula albo-sinensis）+青榨槭（Acer davidii）+岷江冷杉次生针阔混交林（针阔混交林）和青榨槭+红桦+陕甘花楸（Sorbus koehneana Schneid）次生阔叶林（阔叶林）的土壤呼吸及土壤温湿度因子（对照、去除凋落物和加倍凋落物）进行观测。结果显示：去除和加倍凋落物对土壤温湿度的影响不显著,且3种林型之间的土壤呼吸速率差异不显著。与对照相比,去除凋落物使针叶林、针阔混交林、阔叶林的土壤呼吸速率分别降低了17.65%、21.01%和19.83%（P<0.05）;加倍凋落物则分别增加6.76%、7.28%、8.16%（P>0.05）。3种林分土壤呼吸速率均与土壤温度极显著指数相关,与土壤湿度不相关。对照Q₁₀值变幅为2.01-3.29,去除凋落物降低了3种林型的Q₁₀值;加倍凋落物分别提高了针叶林和降低了针阔混交林和阔叶林的Q₁₀值。土壤呼吸速率仅表现在天然次生林对照处理中受到土壤pH、有机质、可溶性有机氮和草本Pielou均匀度指数的显著影响。研究结果表明,天然次生阔叶林和针阔混交林凋落物对土壤呼吸的贡献及Q₁₀值高于天然次生针叶林,说明在未来CO₂浓度及温度升高背景下,地表凋落物增加并未引起天然次生林土壤呼吸速率成倍增加,更有利于该区域天然次生林尤其是针叶林的土壤碳吸存。     

Rise in CO<Subscript>2</Subscript> affects soil water transport through repellency

Several studies have shown improved soil stability under elevated atmospheric CO₂ caused by increased plant and microbial biomass. These studies have not quantified the mechanisms responsible for soil stabilisation or the effect on water relations. The objective of this study was to assess changes in water repellency under elevated CO₂. We hypothesised that increased plant biomass will drive an increase in water repellency, either directly or through secondary microbial processes. Barley plants were grown at ambient (360 ppm) and elevated (720 ppm) CO₂ concentrations in controlled chambers. Each plant was grown in a separate tube of 1.2 m length constructed from 22 mm depth × 47 mm width plastic conduit trunk and packed with sieved arable soil to 55% porosity. After 10 weeks growth the soil was dried at 40°C before measuring water sorptivity, ethanol sorptivity and repellency at many depths with a 0.14 mm radius microinfiltrometer. This provided a microscale measure of the capacity of soil to rewet after severe drying. At testing roots extended throughout the depth of the soil in the tube. The depth of the measurement had no effect on sorptivity or repellency. A rise in CO₂ resulted in a decrease in water sorptivity from 1.13 ± 0.06 (s.e) mm s^−1/2 to 1.00 ± 0.05 mm s^−1/2 (P < 0.05) and an increase in water repellency from 1.80 ± 0.09 to 2.07 ± 0.08 (P < 0.05). Ethanol sorptivity was not affected by CO₂ concentration, suggesting a similar pore structure. Repellency was therefore the primary cause of decreased water sorptivity. The implications will be both positive and negative, with repellency potentially increasing soil stability but also causing patchier wetting of the root-zone.     

Soil plus root respiration and microbial biomass following water, nitrogen, and phosphorus application at a high arctic semi desert

In order to investigate the effects of anticipated increased precipitation and changing soil nutrient levels on soil CO₂ efflux from high arctic semi desert, a field experiment was carried out in Northeast Greenland. Water, phosphorus, and nitrogen were added to plots in a fully factorial design. Soil microbial biomass carbon was analysed after one year, and respiration from soil plus roots was measured in situ throughout the third growing season after initiation of the experiment. Soil plus root respiration was enhanced by up to 47%, and the microbial biomass by 24%, by the weekly water additions, but not by nutrient additions. The direct effect of increased soil moisture on CO₂ efflux suggests that future changes of precipitation levels and patterns may strongly affect below-ground respiration in arctic semi deserts, with direction of responses depending upon amounts and frequencies of precipitation events. Morover, low CO₂ emission at low light intensities regardless of treatment suggests that the major part of the below-ground respiration originated from turnover of recently fixed C. Hence, the more recalcitrant soil organic matter C pool may not change in proportion to changes in below-ground respiration rate.     

Short‐term soil carbon sink potential of oil palm plantations

Oil palm plantations cover ≈14.6 million ha worldwide and the total area under cultivation is expected to increase during the 21st century . Indonesia and Malaysia together account for 87% of global palm oil production and the combined harvested area in these countries has expanded by 6.5 million ha since 1990. Despite this, soil C cycling in oil palm systems is not well quantified but such information is needed for C budget inventories. We quantified soil C storage (root biomass, soil organic matter (SOM) and microbial biomass) and losses [potential soil respiration (R_s) and soil surface CO₂ flux (F_s)] in mineral soils from an oil palm plantation chronosequence (11–34 years since planting) in Selangor, Malaysia. There were no significant effects of plantation age on SOM, microbial biomass, R_s or F_s, implying soil C was in dynamic equilibrium over the chronosequence. However, there was a significant increase in root biomass with plantation age, indicating a short‐term C sink. Across the chronosequence, R_s was driven by soil moisture, soil particle size, root biomass and soil microbial biomass N but not microbial biomass C. This suggests that the nutrient status of the microbial community may be of equal or greater importance for soil CO₂ losses than substrate availability and also raises particular concerns regarding the addition of nitrogenous fertilizer, i.e. increased yields will be associated with increased soil CO₂ emissions. To fully assess the impact of oil palm plantations on soil C storage, initial soil C losses following land conversion (e.g. from native forest or other previous plantations) must be accounted for. If initial soil C losses are large, our data show that there is no accumulation of stable C in the soil as the plantation matures and hence the conversion to oil palm would probably represent a net loss of soil C.     

Transitional slopes act as hotspots of both soil CO<Subscript>2</Subscript> emission and CH<Subscript>4</Subscript> uptake in a temperate forest landscape

Forest soils are an important component of CO₂ and CH₄ fluxes at the global scale, but the magnitude of these fluxes varies greatly in space and time within a landscape. Understanding the spatial and temporal distributions of these fluxes across complex landscapes remains a major challenge for researchers and land managers alike. We investigated the spatiotemporal variability of soil-atmosphere CO₂ and CH₄ fluxes and the relationships of these fluxes to chemical and physical soil properties distributed across a topographically-heterogeneous landscape. Soil CO₂ and CH₄ fluxes were measured along with soil temperature, moisture, bulk density, texture, carbon, sorption capacity, and dissolved organic matter quality over 2 years along hillslope transects spanning valley bottom, transition zone, and upland landscape positions in a temperate forest watershed. Transition zone soil CO₂ efflux was 54–160% higher than low-lying valley bottoms, and 15–54% higher than uplands. Net seasonal CH₄ uptake was 58–150% higher in transition zone soils than in uplands, while valley bottoms were occasionally large net sources (up to 19 nmol CH₄ m^?2 s^?1). Soil CO₂ efflux and net CH₄ uptake were both positively associated with seasonal temperature, and were highest in soils with relatively high carbon and clay content, and relatively low bulk density, moisture, and sorption capacity. We concluded that: (1) transition zone soils act as landscape hotspots for net CH₄ uptake in addition to CO₂ efflux, and (2) that this spatial distribution is more consistent across seasons for net CH₄ uptake than for CO₂ efflux.     

Determinants of growing season soil CO2flux in a Minnesota grassland

Soil CO₂ flux was measured across 947 plots at 7 experimentalgrassland sites at the Cedar Creek Natural History Area in order to determinethe relationships between soil CO₂ flux and environmental factors,living plant biomass, and soil C and N. Soil CO₂ flux increased asthe day progressed, and was positively related to aboveground biomass,belowground biomass, and soil % C. However, most of the variation in soilCO₂ flux explained by a multiple regression model(r ² = 0.55) was attributed to the different experimental sites (61%).Soil CO₂ flux increased with increasing aboveground plant biomass(explaining 16% of the model variation),belowground plant biomass (12%), and soil C and C:N ratio(6%). The length of time between aboveground biomass in aplot was clipped and soil CO₂ flux variedamong plots. Soil CO₂ flux declined with increased timesince clipping, supporting the idea that recently fixedcarbon is a significant component of soil CO₂ flux.Soil CO₂ flux did not follow standard Q₁₀relationships. Over a 20 °C temperature range,soil CO₂ flux tended to be lower in warmer plots.More work is necessary to understand what factors explainthe large differences that were seen among experimentalsites in soil CO₂ flux that could not be explainedby biomass or soil properties.