Post-fire soil respiration in relation to burnt wood management in a Mediterranean mountain ecosystem

After a wildfire, the management of burnt wood may determine microclimatic conditions and microbiological activity with the potential to affect soil respiration. To experimentally analyze the effect on soil respiration, we manipulated a recently burned pine forest in a Mediterranean mountain (Sierra Nevada National and Natural Park, SE Spain). Three representative treatments of post-fire burnt wood management were established at two elevations: (1) “salvage logging” (SL), where all trees were cut, trunks removed, and branches chipped; (2) “non-intervention” (NI), leaving all burnt trees standing; and (3) “cut plus lopping” (CL), a treatment where burnt trees were felled, with the main branches lopped off, but left in situ partially covering the ground surface. Seasonal measurements were carried out over the course of two years. In addition, we performed continuous diurnal campaigns and an irrigation experiment to ascertain the roles of soil temperature and moisture in determining CO₂ fluxes across treatments. Soil CO₂ fluxes were highest in CL (average of 3.34 ± 0.19 μmol m⁻² s⁻¹) and the lowest in SL (2.21 ± 0.11 μmol m⁻² s⁻¹). Across seasons, basal values were registered during summer (average of 1.46 ± 0.04 μmol m⁻² s⁻¹), but increased during the humid seasons (up to 10.07 ± 1.08 μmol m⁻² s⁻¹ in spring in CL). Seasonal and treatment patterns were consistent at the two elevations (1477 and 2317 m a.s.l.), although respiration was half as high at the higher altitude.Respiration was mainly controlled by soil moisture. Watering during the summer drought boosted CO₂ effluxes (up to 37 ± 6 μmol m⁻² s⁻¹ just after water addition), which then decreased to basal values as the soil dried. About 64% of CO₂ emissions during the first 24 h could be attributed to the degasification of soil pores, with the rest likely related to biological processes. The patterns of CO₂ effluxes under experimental watering were similar to the seasonal tendencies, with the highest pulse in CL. Temperature, however, had a weak effect on soil respiration, with Q₁₀ values of ca. 1 across seasons and soil moisture conditions. These results represent a first step towards illustrating the effects of post-fire burnt wood management on soil respiration, and eventually carbon sequestration.     

Reduced soil respiration in gaps in logged lowland dipterocarp forests

We studied the effects of forest composition and structure, and related biotic and abiotic factors on soil respiration rates in a tropical logged forest in Malaysian Borneo. Forest stands were classified into gap, pioneer, non-pioneer and mixed (pioneer, non-pioneer and unclassified trees) based on the species composition of trees >10 cm diameter breast height. Soil respiration rates did not differ significantly between non-gap sites (1290 ± 210 mg CO₂ m⁻² h⁻¹) but were double those in gap sites (640 ± 130 mg CO₂ m⁻² h⁻¹). Post hoc analyses found that an increase in soil temperature and a decrease in litterfall and fine root biomass explained 72% of the difference between gap and non-gap sites. The significant decrease of soil respiration rates in gaps, irrespective of day or night time, suggests that autotrophic respiration may be an important contributor to total soil respiration in logged forests. We conclude that biosphere-atmosphere carbon exchange models in tropical systems should incorporate gap frequency and that future research in tropical forest should emphasize the contribution of autotrophic respiration to total soil respiration.     

Carbon dioxide exchange of a larch forest after a typhoon disturbance

A typhoon event catastrophically destroyed a 45-year-old Japanese larch plantation in southern Hokkaido, northern Japan in September 2004, and about 90% of trees were blown down. Vegetation was measured to investigate its regeneration process and CO₂ flux, or net ecosystem production (NEP), was measured in 2006–2008 using an automated chamber system to investigate the effects of typhoon disturbance on the ecosystem carbon balance. Annual maximum aboveground biomass (AGB) increased from 2.7 Mg ha⁻¹ in 2006 to 4.0 Mg ha⁻¹ in 2007, whereas no change occurred in annual maximum leaf area index (LAI), which was 3.7 m² m⁻² in 2006 and 3.9 m² m⁻² in 2007. Red raspberry (Rubus idaeus) had become dominant within 2 years after the typhoon disturbance, and came to account for about 60% and 50% of AGB and LAI, respectively. In comparison with CO₂ fluxes measured by the eddy covariance technique in 2001–2003, for 4.5 months during the growing season, the sum of gross primary production (GPP) decreased on average by 739 gC m⁻² (64%) after the disturbance, whereas ecosystem respiration (RE) decreased by 501 gC m⁻² (51%). As a result, NEP decreased from 159 ± 57 gC m⁻² to −80 ± 30 gC m⁻², which shows that the ecosystem shifted from a carbon sink to a source. Seasonal variation in RE was strongly correlated to soil temperature. The interannual variation in the seasonal trend of RE was small. Light-saturated GPP (P_max) decreased from 30–45 μmol m⁻² s⁻¹ to 8–12 μmol m⁻² s⁻¹ during the summer season through the disturbance because of large reduction in LAI.     

Implications of fires on carbon budgets in Andean cloud montane forest: The importance of peat soils and tree resprouting

Fire in tropical montane cloud forests (TMCFs) is not as rare as once believed. Andean TMCFs sit immediately below highly flammable, high-altitude grasslands (Puna/Páramo) that suffer from recurrent anthropogenic fire. This treeline is a zone of climatic tension where substantial future warming is likely to force upward tree migrations, while increased fire presence and fire impacts are likely to force it downwards. TMCFs contain large carbon stocks in their peat soils and their loss through fire is a currently unaccounted for regional source of CO₂. This study, conducted in the southern Peruvian Andes (>2800 m), documents differences in live tree biomass, fine root biomass, fallen and standing dead wood, and soil organic carbon in 4 paired-sample plots (burned versus control) following the severe ground fires that occurred during the 2005 Andean drought. Peat soils contributed the most to biomass burning emissions, with lower values corresponding to an 89% mean stock difference compared to the controls (mean ± SE) (54.1 ± 22.3 vs. 5.8 ± 5.3 MgC ha⁻¹). Contrastingly, carbon stocks from live standing trees differed by a non-significant 37% lower value in the burned plots compared to the controls, largely compensated by vigorous resprouting (45.5 ± 17.4 vs. 69.2 ± 13.4 MgC ha⁻¹). Both standing dead trees and fallen dead wood were significantly higher in the burned plots with a three-fold difference from the controls: dead Trees 45.2 ± 9.4 vs. 16.4 ± 4.4 MgC ha⁻¹, and ca. a 2 fold difference for the fallen dead wood: 11.2 ± 5 vs. 6.7 ± 3.2 MgC ha⁻¹ for the burned plots versus their controls. A preliminary estimate of the regional contribution of biomass burning emissions from Andean TMCFs for the period 2000-2008, resulted in mean carbon emission rates of 1.3 TgC yr⁻¹ (max-min: 1.8-0.8 TgC yr⁻¹). This value is in the same order of magnitude than South American annual fire emissions (300 TgC yr⁻¹) suggesting the need for further research on Andean forest fires. On-going projects on the region are working on the promotion of landowner participation in TMCFs conservation through REDD+ mechanism. The heart of the proposed initiative is reforestation of degraded lands with green fire breaks enriched with economically valuable Andean plant species. The cultivation of these species may contribute to reduce deforestation pressure on the Amazonian cloud forest by providing an alternative income to local communities, at the same time that they prevent the spread of fire into Manu National Park and adjacent community-held forests, protecting forest and reducing CO₂ emissions.     

Effects of [CO2] and nitrogen on morphological and biomass traits of white birch (Betula papyrifera) seedlings

To investigate the interactive effects of CO₂ concentration ([CO₂]) and nitrogen supply on the growth and biomass of boreal trees, white birch seedlings (Betula papyrifera) were grown under ambient (360 μmol mol⁻¹) and elevated [CO₂] (720 μmol mol⁻¹) with five nitrogen supply regimes (10, 80, 150, 220, and 290 μmol mol⁻¹) in greenhouses. After 90 days of treatment, seedling height, root-collar diameter, biomass of different organs, leaf N concentration, and specific leaf area (SLA) were measured. Significant interactive effects of [CO₂] and N supply were found on height, root-collar diameter, leaf biomass, stem biomass and total biomass, stem mass ratio (SMR), and root mass ratio (RMR), but not on root mass, leaf mass ratio (LMR), leaf to root ratio (LRR), or leaf N concentration. The CO₂ elevation generally increased all the growth and biomass parameters and the increases were generally greater at higher levels of N supply or higher leaf N concentration. However, the CO₂ elevation significantly reduced SLA (13.4%) and mass-based leaf N concentration but did not affect area-based leaf N concentration. Increases in N supply generally increased the growth and biomass parameters, but the relationships were generally curvilinear. Based on a second order polynomial model, the optimal leaf N concentration was 1.33 g m⁻² for height growth under ambient [CO₂] and 1.52 g m⁻² under doubled [CO₂]; 1.48 g m⁻² for diameter under ambient [CO₂] and 1.64 g m⁻² under doubled [CO₂]; 1.29 g m⁻² for stem biomass under ambient [CO₂] and 1.43 g m⁻² under doubled [CO₂]. The general trend is that the optimal leaf N was higher at doubled than ambient [CO₂]. However, [CO₂] did not affect the optimal leaf N for leaf and total biomass. The CO₂ elevation significantly increased RMR and SMR but decreased LMR and LRR. LMR increased and RMR decreased with the increasing N supply. SMR increased with increase N supply up to 80 μmol mol⁻¹ and then leveled off (under elevated [CO₂]) or stated to decline (under ambient [CO₂]) with further increases in N supply. The results suggest that the CO₂ elevation increased biomass accumulation, particularly stem biomass and at higher N supply. The results also suggest that while modest N fertilization will increase seedling growth and biomass accumulation, excessive application of N may not stimulate further growth or even result in growth decline.     

Soil–atmosphere CO2, CH4 and N2O fluxes in boreal forestry-drained peatlands

Greenhouse gas emissions from managed peatlands are annually reported to the UNFCCC. For the estimation of greenhouse gas (GHG) balances on a country-wide basis, it is necessary to know how soil–atmosphere fluxes are associated with variables that are available for spatial upscaling. We measured momentary soil–atmosphere CO₂ (heterotrophic and total soil respiration), CH₄ and N₂O fluxes at 68 forestry-drained peatland sites in Finland over two growing seasons. We estimated annual CO₂ effluxes for the sites using site-specific temperature regressions and simulations in half-hourly time steps. Annual CH₄ and N₂O fluxes were interpolated from the measurements. We then tested how well climate and site variables derived from forest inventory results and weather statistics could be used to explain between-site variation in the annual fluxes. The estimated annual CO₂ effluxes ranged from 1165 to 4437 g m⁻² year⁻¹ (total soil respiration) and from 534 to 2455 g m⁻² year⁻¹ (heterotrophic soil respiration). Means of 95% confidence intervals were ±12% of total and ±22% of heterotrophic soil respiration. Estimated annual CO₂ efflux was strongly correlated with soil respiration at the reference temperature (10 °C) and with summer mean air temperature. Temperature sensitivity had little effect on the estimated annual fluxes. Models with tree stand stem volume, site type and summer mean air temperature as independent variables explained 56% of total and 57% of heterotrophic annual CO₂ effluxes. Adding summer mean water table depth to the models raised the explanatory power to 66% and 64% respectively. Most of the sites were small CH₄ sinks and N₂O sources. The interpolated annual CH₄ flux (range: −0.97 to 12.50 g m⁻² year⁻¹) was best explained by summer mean water table depth (r² = 64%) and rather weakly by tree stand stem volume (r² = 22%) and mire vegetation cover (r² = 15%). N₂O flux (range: −0.03 to 0.92 g m⁻² year⁻¹) was best explained by peat CN ratio (r² = 35%). Site type explained 13% of annual N₂O flux. We suggest that water table depth should be measured in national land-use inventories for improving the estimation of country-level GHG fluxes for peatlands.     

Estimations of total ecosystem carbon pools distribution and carbon biomass current annual increment of a moist tropical forest

With increasing CO₂ in the atmosphere, there is an urgent need of reliable estimates of biomass and carbon pools in tropical forests, most especially in Africa where there is a serious lack of data. Information on current annual increment (CAI) of carbon biomass resulting from direct field measurements is crucial in this context, to know how forest ecosystems will affect the carbon cycle and also to validate eddy covariance flux measurements. Biomass data were collected from 25 plots of 13 ha spread over the different vegetation types and land uses of a moist evergreen forest of 772,066 ha in Cameroon. With site-specific allometric equations, we estimated biomass and aboveground and belowground carbon pools. We used GIS technology to develop a carbon biomass map of our study area. The CAI was estimated using the growth rates obtained from tree rings analysis. The carbon biomass was on average 264 ± 48 Mg ha⁻¹. This estimate includes aboveground carbon, root carbon and soil organic carbon down to 30 cm depth. This value varied from 231 ± 45 Mg ha⁻¹ of carbon in Agro-Forests to 283 ± 51 Mg ha⁻¹ of carbon in Managed Forests and to 278 ± 56 Mg ha⁻¹ of carbon in National Park. The carbon CAI varied from 2.54 ± 0.65 Mg ha⁻¹ year⁻¹ in Agro-Forests to 2.79 ± 0.72 Mg ha⁻¹ year⁻¹ in Managed Forests and to 2.85 ± 0.72 Mg ha⁻¹ year⁻¹ in National Park. This study provides estimates of biomass, carbon pools and CAI of carbon biomass from a forest landscape in Cameroon as well as an appropriate methodology to estimate these components and the related uncertainty.     

An ecosystem approach to biodiversity effects: Carbon pools in a tropical tree plantation

This paper presents a synthesis of experiments conducted in a tropical tree plantation established in 2001 and consisting of 22 plots of 45 m × 45 m with either one, three or six native tree species. We examined the changes in carbon (C) pools (trees, herbaceous vegetation, litter, coarse woody debris (CWD), and mineral topsoil at 0-10 cm depth) and fluxes (decomposition of CWD and litter, as well as soil respiration) both through time and among diversity levels. Between 2001 and 2009 the aboveground C pools increased, driven by trees. Across diversity levels, the mean observed aboveground C pool was 7.9 ± 2.5 Mg ha⁻¹ in 2006 and 20.4 ± 7.4 Mg ha⁻¹ in 2009, a 158% increase. There was no significant diversity effect on the observed aboveground C pool, but we found a significant decrease in the topsoil C pool, with a mean value of 34.5 ± 2.4 Mg ha⁻¹ in 2001 and of 25.7 ± 5.7 Mg ha⁻¹ in 2009 (F_1,36 = 52.12, p < 0.001). Assuming that the biomass C pool in 2001 was negligible (<1 Mg ha⁻¹), then the plantation gained in C, on average, ∼20 and lost ∼9 Mg ha⁻¹ in biomass and soil respectively, for an overall gain of ∼11 Mg ha⁻¹ over 8 years. Across the entire data set, we uncovered significant effects of diversity on CWD decomposition (diversity: F_2,393 = 15.93, p < 0.001) and soil respiration (monocultures vs mixtures: t = 15.35, df = 11, p < 0.05) and a marginally significant time × diversity interaction on the loss of total C from the mineral topsoil pool (see above). Monthly CWD decomposition was significantly faster in monocultures (35.0 ± 24.1%) compared with triplets (31.3 ± 21.0%) and six-species mixtures (31.9 ± 26.8%), while soil respiration was higher in monocultures than in mixtures (t = 15.35, df = 11, p < 0.001). Path analyses showed that, as diversity increases, the links among the C pools and fluxes strengthen significantly. Our results demonstrate that tree diversity influences the processes governing the changes in C pools and fluxes following establishment of a tree plantation on a former pasture. We conclude that the choice of tree mixtures for afforestation in the tropics can have a marked influence on C pools and dynamics.     

Carbon and nitrogen cycling immediately following bark beetle outbreaks in southwestern ponderosa pine forests

Bark beetle infestation is a well-known cause of historical low-level disturbance in southwestern ponderosa pine forests, but recent fire exclusion and increased tree densities have enabled large-scale bark beetle outbreaks with unknown consequences for ecosystem function. Uninfested and beetle-infested plots (n = 10 pairs of plots on two aspects) of ponderosa pine were compared over one growing season in the Sierra Ancha Experimental Forest, AZ to determine whether infestation was correlated with differences in carbon (C) and nitrogen (N) pools and fluxes in aboveground biomass and soils. Infested plots had at least 80% of the overstory ponderosa pine trees attacked by bark beetles within 2 years of our measurements. Both uninfested and infested plots stored ∼9 kg C m⁻² in aboveground tree biomass, but infested plots held 60% of this aboveground tree biomass in dead trees, compared to 5% in uninfested plots. We hypothesized that decreased belowground C allocation following beetle-induced tree mortality would alter soil respiration rates, but this hypothesis was not supported; throughout the growing season, soil respiration in infested plots was similar to uninfested plots. In contrast, several results supported the hypothesis that premature needlefall from infested trees provided a pulse of low C:N needlefall that altered soil N cycling. The C:N mass ratio of pine needlefall in infested plots (∼45) was lower than uninfested plots (∼95) throughout the growing season. Mineral soils from infested plots had greater laboratory net nitrification rates and field resin bag ammonium accumulation than uninfested plots. As bark beetle outbreaks become increasingly prevalent in western landscapes, longer-term biogeochemical studies on interactions with other disturbances (e.g. fire, harvesting, etc.) will be required to predict changes in ecosystem structure and function.     

Influences of forest tending works on carbon distribution and cycling in a Pinus densiflora S. et Z. stand in Korea

This study was conducted to determine carbon (C) dynamics following forest tending works (FTW) which are one of the most important forest management activities conducted by Korean forest police and managers. We measured organic C storage (above- and below-ground biomass C, forest floor C, and soil C at 50 cm depth), soil environmental factors (soil CO₂ efflux, soil temperature, soil water content, soil pH, and soil organic C concentration), and organic C input and output (litterfall and litter decomposition rates) for one year in FTW and non-FTW (control) stands of approximately 40-year-old red pine (Pinus densiflora S. et Z.) forests in the Hwangmaesan Soopkakkugi model forest in Sancheonggun, Gyeongsangnam-do, Korea. This forest was thinned in 2005 as a representative FTW practice. The total C stored in tree biomass was significantly lower (P < 0.05) in the FTW stand (40.17 Mg C ha⁻¹) than in the control stand (64.52 Mg C ha⁻¹). However, C storage of forest floor and soil layers measured at four different depths was not changed by FTW, except for that at the surface soil depth (0–10 cm). The organic C input due to litterfall and output due to needle litter decomposition were both significantly lower in the FTW stand than in the control stand (2.02 Mg C ha⁻¹ year⁻¹ vs. 2.80 Mg C ha⁻¹ year⁻¹ and 308 g C kg⁻¹ year⁻¹ vs. 364 g C kg⁻¹ year⁻¹, respectively, both P < 0.05). Soil environmental factors were significantly affected (P < 0.05) by FTW, except for soil CO₂ efflux rates and organic C concentration at soil depth of 0–20 cm. The mean annual soil CO₂ efflux rates were the same in the FTW (0.24 g CO₂ m⁻² h⁻¹) and control (0.24 g CO₂ m⁻² h⁻¹) stands despite monthly variations of soil CO₂ efflux over the one-year study period. The mean soil organic C concentration at a soil depth of 0–20 cm was lower in the FTW stand (81.3 g kg⁻¹) than in the control stand (86.4 g kg⁻¹) but the difference was not significant (P > 0.05). In contrast, the mean soil temperature was significantly higher, the mean soil water content was significantly lower, and the soil pH was significantly higher in the FTW stand than in the control stand (10.34 °C vs. 8.98 °C, 48.2% vs. 56.4%, and pH 4.83 vs. pH 4.60, respectively, all P < 0.05). These results indicated that FTW can influence tree biomass C dynamics, organic C input and output, and soil environmental factors such as soil temperature, soil water content and soil pH, while soil C dynamics such as soil CO₂ efflux rates and soil organic C concentration were little affected by FTW in a red pine stand.     

Carbon accumulation in the biomass and soil of different aged secondary forests in the humid tropics of Costa Rica

Efforts are needed in order to increase confidence for carbon accounts in the land use sector, especially in tropical forest ecosystems that often need to turn to default values given the lack of precise and reliable site specific data to quantify their carbon sequestration and storage capacity. The aim of this study was then to estimate biomass and carbon accumulation in young secondary forests, from 4 and up to 20 years of age, as well as its distribution among the different pools (tree including roots, herbaceous understory, dead wood, litter and soil), in humid tropical forests of Costa Rica. Carbon fraction for the different pools and tree components (stem, branches, leaves and roots) was estimated and varies between 37.3% (±3.3) and 50.3% (±2.9). Average carbon content in the soil was 4.1% (±2.1). Average forest plant biomass was 82.2 (±47.9) Mg ha⁻¹ and the mean annual increment for carbon in the biomass was 4.2 Mg ha⁻¹ yr⁻¹. Approximately 65.2% of total biomass was found in the aboveground tree components, while 14.2% was found in structural roots and the rest in the herbaceous vegetation and necromass. Carbon in the soil increased by 1.1 Mg ha⁻¹ yr⁻¹. Total stored carbon in the forest was 180.4 Mg ha⁻¹ at the age of 20 years. In these forests, most of the carbon (51-83%) was stored in the soil. Models selected to estimate biomass and carbon in trees as predicted by basal area had R² adjustments above 95%. Results from this study were then compared with those obtained for a variety of secondary and primary forests in different Latin-American tropical ecosystems and in tree plantations in the same study area.     

Impacts of understory species removal and/or addition on soil respiration in a mixed forest plantation with native species in southern China

Although the removal or addition of understory vegetation has been an important forest management practice in forest plantations, the effects of this management practice on soil respiration are unclear. The overall objective of this study was to measure and model soil respiration and its components in a mixed forest plantation with native species in south China and to assess the effects of understory species management on soil respiration and on the contribution of root respiration (R_r) to total soil respiration (R_s). An experiment was conducted in a plantation containing a mixture of 30 native tree species and in which understory plants had been removed or replaced by Cassia alata Linn. The four treatments were the control (Control), C. alata addition (CA), understory removal (UR) and understory removal with C. alata addition (UR + CA). Trenched subplots were used to quantify R_r by comparing R_s outside the 1-m² trenched subplots (plants and roots present) and inside the trenched subplots (plants and roots absent) in each treatment. Annual soil respiration were modeled using the values measured for R_s, soil temperature and soil moisture. Our results indicate that understory removal reduced R_s rate and soil moisture but increased soil temperature. Regression models revealed that soil temperature was the main factor and soil moisture was secondary. Understory manipulations and trenching increased the temperature sensitivity of R_s. Annual R_s for the Control, CA, UR and UR + CA treatments averaged 594, 718, 557 and 608 g C m⁻² yr⁻¹, respectively. UR decreased annual R_s by 6%, but CA increased R_s by about 21%. Our results also indicate that management of understory species increased the contribution of R_r to R_s.     

Soil respiration and microbial biomass in a pecan — cotton alley cropping system in Southern USA

Little information is available on soil respiration and microbial biomass in soils under agroforestry systems. We measured soil respiration rate and microbial biomass under two age classes (young and old) of a pecan (Carya illinoinensis) — cotton (Gossypium hirsutum) alley cropping system, two age classes of pecan orchards, and a cotton monoculture on a well-drained, Redbay sandy loam (a fine-loamy, siliceous, thermic Rhodic Paleudult) in southern USA. Soil respiration was quantified monthly during the growing season from May to November 2001 using the soda-lime technique and was corrected based on infrared gas analyzer (IRGA) measurements. The overall soil respiration rates ranged from 177 to 776 mg CO₂ m^–2 h^–1. During the growing season, soil respiration was higher in the old alley cropping system than in the young alley cropping system, the old pecan orchard, the young pecan orchard, and the monoculture. Microbial biomass C was higher in the old alley cropping system (375 mg C kg^–1) and in the old pecan orchard (376 mg C kg^–1) compared to the young alley cropping system (118 mg C kg^–1), young pecan orchard (88 mg C kg^–1), and the cotton monoculture (163 mg C kg^–1). Soil respiration was correlated positively with soil temperature, microbial biomass, organic matter, and fine root biomass. The effect of alley cropping on soil properties during the brief history of alley cropping was not significant except in the old systems, where there was a trend of increasing soil respiration with short-term alley cropping. Over time, different land use and management practices influenced soil properties such as soil temperature, moisture, microbial biomass, organic matter, and fine root biomass, which in turn affected the magnitude of soil respiration. Our results suggest that trees in agroforestry systems have the potential to enhance soil fertility and sustainability of farmlands by improving soil microbial activity and accreting residual soil carbon.This revised version was published online in November 2005 with corrections to the Cover Date.     

杉木纯林、混交林土壤微生物特性和土壤养分的比较研究

本文于2005年5月份,在中国科学院会同森林生态实验站选择了一块15年生的杉木纯林和两块15年生杉阔混交林作为研究对象,调查了林地土壤有机碳、全氮、全磷、硝态氮、有效磷和土壤微生物碳、氮、磷、基础呼吸以及呼吸熵,比较了纯林和混交林土壤微生物特性和土壤养分.结果表明,杉阔混交林的土壤有机碳、全氮、全磷硝态氮和有效磷含量高于杉木纯林;在混交林中,土壤微生物学特性得到改善.在0(10 cm和10(20 cm两层土壤中,杉阔混交林土壤微生物氮含量分别比杉木纯林高69%和61%.在0(10 cm土层,杉阔混交林土壤微生物碳、磷和基础呼吸分别比杉木纯林高11%、14%和4%;在10(20 cm土层,分别高6%、3%和3%.但是,杉阔混交林土壤微生物碳:氮比和呼吸熵较杉木纯林低34%和4%.另外,土壤微生物与土壤养分的相关性高于土壤呼吸、微生物碳:氮比和呼吸熵与土壤养分的相关性.由此可知,在针叶纯林中引入阔叶树后,土壤肥力得以改善,并有利于退化森林土壤的恢复.     

Comparison of soil CO2 flux between uncleared and cleared windthrow areas in Estonia and Latvia

Storms can turn a great proportion of forests’ assimilation capacity into dead organic matter because of windthrow and thus its role as a carbon sink will be diminished for some time. However, little is known about the magnitude or extent to which storms affect carbon efflux. We compared soil CO₂ fluxes in wind-thrown forest stands with different time periods since a storm event, and with different management practices (deadwood cleared or left on-site). This study examined changes in soil CO₂ efflux in two windthrow areas in north-eastern Estonia and one area in north-western Latvia, which experienced severe wind storms in the summers of 2001, 2002 and 1967, respectively. We measured soil CO₂ fluxes in stands formerly dominated by Norway spruce (Picea abies L. Karst.) with total and partial canopy destruction (all trees or roughly half of the trees in stand damaged by storm), in harvested areas (material removed after the wind storm) and in control areas (no damage by wind). Removal of wind-damaged material decreased instantaneous CO₂ flux from the soil surface. The highest instantaneous fluxes were measured in areas with total and partial canopy destruction (0.67 g CO₂ m⁻² h⁻¹ in both cases) compared with fluxes in the control areas (0.51 g CO₂ m⁻² h⁻¹), in the new storm-damaged areas where the material was removed (0.57 g CO₂ m⁻² h⁻¹) and in the old storm-damaged area where wood was left on site (0.55 g CO₂ m⁻² h⁻¹). The only factor affecting soil CO₂ flux was location of the measuring collar (plastic collar with diameter 100 mm, height 50 mm) - either on undamaged forest ground or on the uprooted tree pit, where the mineral soil was exposed after disturbance. New wind-thrown stands where residues are left on site would most likely turn to sources of CO₂ for several years until forest regeneration reaches to substantial assimilation rates. New wind-thrown stands where residues are left on site would most likely tend to have elevated CO₂ fluxes for several years until forest regeneration reaches to substantial assimilation rates. However, forest managers might be concerned about the amounts of CO₂ immediately released into the atmosphere if the harvested logs are burned.     

Root trenching: a useful tool to estimate autotrophic soil respiration? A case study in an Austrian mountain forest

We conducted a trenching experiment in a mountain forest in order to assess the contribution of the autotrophic respiration to total soil respiration and evaluate trenching as a technique to achieve it. We hypothesised that the trenching experiment would alter both microbial biomass and microbial community structure and that fine roots (less than 2 mm diameter) would be decomposed within one growing season. Soil CO₂ efflux was measured roughly biweekly over two growing seasons. Root presence and morphology parameters, as well as the soil microbial community were measured prior to trenching, 5 and 15 months after trenching. The trenched plots emitted about 20 and 30% less CO₂ than the control plots in the first and second growing season, respectively. Roots died in trenched plots, but root decay was slow. After 5 and 15 months, fine root biomass was decreased by 9% (not statistically different) and 30%, (statistically different) respectively. When we corrected for the additional trenched-plot CO₂ efflux due to fine root decomposition, the autotrophic soil respiration rose to ~26% of the total soil respiration for the first growing season, and to ~44% for the second growing season. Soil microbial biomass and community structure was not altered by the end of the second growing season. We conclude that trenching can give accurate estimates of the autotrophic and heterotrophic components of soil respiration, if methodological side effects are accounted for, only.     

Soil and microbial respiration in a loblolly pine plantation in response to seven years of irrigation and fertilization

Because soil CO₂ efflux or soil respiration (R_S) is the major component of forest carbon fluxes, the effects of forest management on R_S and microbial biomass carbon (C), microbial respiration (R_H), microbial activity and fine root biomass were studied over two years in a loblolly pine (Pinus taeda L.) plantation located near Aiken, SC. Stands were six-years-old at the beginning of the study and were subjected to irrigation (no irrigation versus irrigation) and fertilization (no fertilization versus fertilization) treatments since planting. Soil respiration ranged from 2 to 6 μmol m⁻² s⁻¹ and was strongly and linearly related to soil temperature. Soil moisture and C inputs to the soil (coarse woody debris and litter mass) which may influence R_H were significantly but only weakly related to R_S. No interaction effects between irrigation and fertilization were observed for R_S and microbial variables. Irrigation increased R_S, fine root mass and microbial biomass C. In contrast, fertilization increased R_H, microbial biomass C and microbial activity but reduced fine root biomass and had no influence on R_S. Predicted annual soil C efflux ranged from 8.8 to 10.7 Mg C ha⁻¹ year⁻¹ and was lower than net primary productivity (NPP) in all stands except the non-fertilized treatment. The influence of forest management on R_S was small or insignificant relative to biomass accumulation suggesting that NPP controls the transition between a carbon source and sink in rapidly growing pine systems.     

Above-ground biomass dynamics after reduced-impact logging in the Eastern Amazon

Changes in above-ground biomass (AGB) of 17 1 ha logged plots of terra firme rain forest in the eastern Amazon (Brazil, Paragominas) were monitored for four years (2004–2008) after reduced-impact logging. Over the same time period, we also monitored two 0.5 ha plots in adjacent unlogged forest. While AGB in the control plots changed little over the observation period (increased on average 1.4 Mg ha⁻¹), logging resulted in immediate reductions in ABG that averaged 94.5 Mg ha⁻¹ (±42.0), which represented 23% of the 410 Mg ha⁻¹ (±64.9) present just prior to harvesting. Felled trees (dbh > 55 cm) accounted for 73% (±15) of these immediate losses but only 18.9 Mg ha⁻¹ (±8.1) of biomass was removed in the extracted logs. During the first year after logging, the annual AGB balance (annual AGB gain by recruitment and growth − annual AGB loss by mortality) remained negative (−31.1 Mg ha⁻¹ year⁻¹; ±16.7), mainly due to continued high mortality rates of damaged trees. During the following three years (2005–2008), average net AGB accumulation in the logged plots was 2.6 Mg ha⁻¹ year⁻¹ (±4.6). Post-logging biomass recovery was mostly through growth (4.3 ± 1.5 Mg ha⁻¹ year⁻¹ for 2004–2005 and 6.8 ± 0.9 Mg ha⁻¹ year⁻¹ for 2005–2008), particularly of large trees. In contrast, tree recruitment contributed little to the observed increases in AGB (1.1 ± 0.6 Mg ha⁻¹ year⁻¹ for 2004–2005 and 3.1 ± 1.3 Mg ha⁻¹ year⁻¹ for 2005–2008). Plots with the lowest residual basal area after logging generally continued to lose more large trees (dbh ≥70 cm), and consequently showed the greatest AGB losses and the slowest overall AGB gains. If 100% AGB recovery is desired and the 30-year minimum cutting cycle defined by Brazilian law is adhered to, current logging intensities (6 trees ha⁻¹) need to be reduced by 40–50%. Such a reduction in logging intensity will reduce financial incomes to loggers, but might be compensated for by the payment of environmental services through the proposed REDD (reduced emissions from deforestation and forest degradation) mechanism of the United Nations Framework Convention on Climate Change.     

Partitioning of soil respiration into its autotrophic and heterotrophic components by means of tree-girdling in old boreal spruce forest

Forests accumulate much less carbon than the amount fixed through photosynthesis because of an almost equally large opposing flux of CO₂ from the ecosystem. Most of the return flux to the atmosphere is through soil respiration, which has two major sources, one heterotrophic (organisms decomposing organic matter) and one autotrophic (roots, mycorrhizal fungi and other root-associated microbes dependent on recent photosynthate). We used tree-girdling to stop the flow of photosynthate to the belowground system, hence, blocking autotrophic soil activity in a 120-yr-old boreal Picea abies forest. We found that at the end of the summer, two months after girdling, the treatment had reduced soil respiration by up to 53%. This figure adds to a growing body of evidence indicating (t-test, d.f. = 7, p < 0.05) that autotrophic respiration may contribute more to total soil respiration in boreal (mean 53 ± 2%) as compared to temperate forests (mean 44 ± 3%). Our data also suggests that there is a seasonal hysteresis in the response of total soil respiration to changes in temperature. We propose that this reflects seasonality in the tree below-ground carbon allocation.     

Effects of winter selective tree harvest on soil microclimate and surface CO2 flux of a northern hardwood forest

Soil surface CO₂ flux (S_flux) is the second largest terrestrial ecosystem carbon flux, and may be affected by forest harvest. The effects of clearcutting on S_flux have been studied, but little is known about the effect of alternative harvesting methods such as selective tree harvest on S_flux. We measured S_flux before and after (i) the creation of forest canopy gaps (simulating group tree selection harvests) and (ii) mechanized winter harvest but no tree removal (simulating ground disturbance associated with logging). The experiment was carried out in a sugar maple dominated forest in the Flambeau River State Forest, Wisconsin. Pre-treatment measurements of soil moisture, temperature and S_flux were measured throughout the growing season of 2006. In January–February 2007, a harvester created the canopy gaps (200–380 m²). The mechanization treatment consisted of the harvester traveling through the plots for a similar amount of time as the gap plots, but no trees were cut. Soil moisture and temperature and S_flux were measured throughout the growing season for 1 year prior to harvest and for 2 years after harvest. Soil moisture and temperature were significantly greater in the gap than mechanized and control treatments. Instantaneous S_flux was positively correlated to soil moisture and soil temperature at 2 and 10 cm, but temperature at 10 cm was the single best predictor. Annual S_flux was not significantly different among treatments prior to winter 2007 harvest, and was not significantly different among treatments after harvest. Annual (+1 std. err.) S_flux averaged 967 + 72, 1011 + 72, and 1012 + 72 g C m⁻² year⁻¹ in the control, mechanized and gap treatments, respectively, for the 2-year post-treatment period. The results from this study suggest selective group tree harvest significantly increases soil moisture and temperature but does not significantly influence S_flux.