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.     

The effect of land use type on net nitrogen mineralization on abandoned agricultural land: Silver birch stand versus grassland

The effect of land use type on the dynamics and annual rate of net nitrogen mineralization (NNM) in a naturally generated silver birch stand and in a grassland, both on abandoned agricultural land, was assessed in situ in the upper 0–20 cm soil layer using the method of buried polyethylene bags. Annual NNM rate in the birch stand (156 kg N ha⁻¹ year⁻¹) was higher than in the grassland (102 kg N ha⁻¹ year⁻¹); in both cases NNM covered a major part of the plants annual nitrogen demand. The rate of NNM in the upper 0–10 cm soil layer in the birch stand (99 kg N ha⁻¹ year⁻¹) exceeded the respective rate of NNM in the grassland (51 kg N ha⁻¹ year⁻¹) roughly two times. In the grassland the rates of NNM in the 0–10 and 10–20 cm layers were equal; in the birch stand NNM in the 0–10 cm layer was 1.7 times higher than in deeper 10–20 cm layer. The intensity of daily NNM in the upper 0–10 cm soil layer in the birch stand was the highest in June and in the grassland in May, 776 and 528 mg kg⁻¹ N day⁻¹, respectively. In our study no significant correlation was found between NNM and the environmental factors monthly mean soil temperature, soil moisture content and pH.     

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.     

Allometric equations for tree species and carbon stocks for forests of northwestern Mexico

Allometric equations were developed and applied to forest inventory data to estimate biomass and carbon stocks for temperate species and forests of Durango and Chihuahua and for tropical dry forests of Sinaloa, Mexico. A total of 872 trees were harvested and dissected into their component parts: leaves and branches, boles, and coarse roots. Coarse roots of 40 temperate trees ranging in diameter at breast height (DBH) from 6.0 to 52.9 cm were excavated in their entirety (i.e., >0.5 cm diameter). The species sampled (number of trees) in tropical dry forests (39) were Lysiloma divaricata (Jacq) Macbr. (10), Haematoxylon brasiletto Karst. (10), Cochlospermum vitifolium (Wild.) (5), Ceiba acuminata (S. Watson) Rose (5), Bursera penicillata (B. inopinnata) (5), and Jatropha angustifolia Mull. Arg. (4) and in temperate forests (833) were Quercus spp. (118) (Q. rugosa Neé, 15, Quercus sideroxylla Humb. & Bonpl, 51, Quercus spp., 52), Pinus herrerae Martinez 1940 (19), Pinus oocarpa Schiede ex Schlectendal 1838 (31), Pinus engelmannii Carriere 1854 (7), Psudotsuga menziesii (Mirb.) Franco (19), Pinus leiophylla Schiede ex Schlectendal et Chamisso 1831 (27), Pinus teocote Schiede ex Schlectendal et Chamisso (55), Pinus ayacahuite Ehrenb. ex Schltdl. (58), Pinus cooperi Blanco (48), Pinus durangensis Martinez 1942 (385), and Pinus arizonica Engelmann 1879 (66). Allometric equations having only DBH as an independent variable were developed for each component of each species. Since Pinus herrerae, Pinus engelmannii, Pinus oocarpa and Pseudotsuga menziensii had a small number of trees, an individual allometric equation was developed for these species. We used non-linear regression to fit parameters of the typical allometric power equation. The resulting 31 equations (10 species or groups of species, three biomass components; bole, branch and leaves, and total aerial; and the generalized equation for coarse roots) fit the data well and enable the user to predict biomass by component for each of the 10 different groups of species or each of six temperate species. A single allometric equation that incorporates the basic specific gravity for aboveground biomass of all temperate tree species also fit the data well, and this equation provides both the detail and the accuracy supplied by species-specific, plant-part-specific equations. Biomass equations coupled with forest inventory data for temperate (637 circular, 1/10 ha plots) and tropical dry forests (166 20 m × 20 m-quadrats) of northwestern Mexico predict a mean (confidence intervals) of 130 Mg ha⁻¹ (4.2 Mg ha⁻¹) and 73 Mg ha⁻¹ (7.1 Mg ha⁻¹) for total tree and total aboveground biomass, respectively. Large sample sizes and the economic and ecological importance of the species studied make this data set uniquely useful for biomass estimations and for understanding the inherent heterogeneity of tree structure in dynamic tropical and temperate environments of northwestern Mexico.     

Net primary productivity of Bruguiera parviflora (Wight & Arn.) dominated mangrove forest at Kuala Selangor,Malaysia

The net primary productivity of Bruguiera parviflora dominated mangrove forest at Kuala Selangor, Malaysia was estimated from the average yearly biomass increment and litter production. The average yearly biomass increment in saplings and trees was 0.58 and 16.51 t ha⁻¹, respectively, and the annual amount of total litter production was 10.35 t ha⁻¹. The biomass increment in saplings and trees was not significantly different (t-test, p > 0.05) in 2 successive years and the estimated net primary productivity was 27.44 t ha⁻¹ year⁻¹. The ratio (2.65:1) of net primary productivity and litterfall suggests that this mangrove forest is at a juvenile stage.     

Effect of species and spacing of fast-growing nurse trees on growth of an indigenous tree, Hopea odorata Roxb., in northeast Thailand

We tested the effects of species and spacing of nurse trees on the growth of Hopea odorata, a dipterocarp tree indigenous to Southeast Asia, in a two-storied forest management system in northeast Thailand. Eucalyptus camaldulensis, Acacia auriculiformis, and Senna siamea were planted as nurse trees in 1987 at spacings of 4 m × 8 m, 2 m × 8 m, 4 m × 4 m, and 2 m × 4 m in the Sakaerat Silvicultural Research Station of the Royal Forest Department, Thailand. Seedlings of H. odorata were planted in the nurse tree stands at a uniform spacing of 4 m × 4 m and in control plots (no nurse trees) in 1990. Stem numbers of some nurse trees were thinned by half in 1994. The stem diameter and height of all trees were measured annually until 1995 and again in 2007. The mean annual increment (MAI) in volume was estimated as 8.2–10.1 m³ ha⁻¹ year⁻¹ for E. camaldulensis and 0.9–1.2 m³ ha⁻¹ year⁻¹ for S. siamea, smaller than reported elsewhere. This suggests that the site properties were not suitable for them. The MAI of A. auriculiformis was 7.9–9.8 m³ ha⁻¹ year⁻¹, within the reported range. Survival rates of H. odorata in the S. siamea stands and the control plots decreased rapidly during the first 2 years but then stayed constant from 1992. In contrast, survival rates of H. odorata in the E. camaldulensis and A. auriculiformis stands were initially high (>70%), but then decreased after 1995. Stem diameter, tree height, and stand basal area of H. odorata were large in both the S. siamea stands and the control plots from then. The growth of H. odorata was largest in the 2 m × 8 m S. siamea stands. In contrast, it was restricted in the E. camaldulensis and A. auriculiformis stands owing to strong shading by their canopies. Thinning by 50% tended to facilitate the growth of H. odorata temporarily in the E. camaldulensis and A. auriculiformis stands. The stand basal areas of nurse trees and of H. odorata showed a trade-off. These results suggest that the growth of H. odorata was maximized in the S. siamea stands. We assume, however, that the growth of H. odorata could be improved even in the E. camaldulensis and A. auriculiformis stands by frequent or heavy thinning.     

Water use by Tabor and Kermes oaks growing in their respective habitats in the Lower Galilee region of Israel

We estimated water use by the two main oak species of the Lower Galilee region of Israel—Tabor (Quercus ithaburensis) and Kermes (Quercus calliprinos)—to develop management options for climate-change scenarios. The trees were studied in their typical phytosociological associations on different bedrock formations at two sites with the same climatic conditions. Using the heat-pulse method, sap flow velocity was measured in eight trunks (trees) of each species during a number of periods in 2001, 2002 and 2003. Hourly sap flux was integrated to daily transpiration per tree and up-scaled to transpiration at the forest canopy level. The annual courses of daytime transpiration rate were estimated using fitted functions, and annual totals were calculated. Sap flow velocity was higher in Tabor than in Kermes oak, and it was highest in the youngest xylem, declining with depth into the older xylem. Average daytime transpiration rate was 67.9 ± 4.9 l tree⁻¹ d⁻¹, or 0.95 ± 0.07 mm d⁻¹, for Tabor oak, and 22.0 ± 1.7 l tree⁻¹d⁻¹, or 0.73 ± 0.05 mm d⁻¹, for Kermes oak. Differences between the two oak species in their forest canopy transpiration rates occurred mainly between the end of April and the beginning of October. Annual daytime transpiration was estimated to be 244 mm year⁻¹ for Tabor oak and 213 mm year⁻¹ for Kermes oak. Adding nocturnal water fluxes, estimated to be 20% of the daytime transpiration, resulted in total annual transpiration of 293 and 256 mm year⁻¹ by Tabor and Kermes oaks, respectively. These amounts constituted 51% and 44%, respectively, of the 578 mm year⁻¹ average annual rainfall in the region. The two species differed in their root morphology. Tabor oak roots did not penetrate the bedrock but were concentrated along the soil–rock interface within soil pockets. In contrast, the root system of Kermes oak grew deeper via fissures and crevices in the bedrock system and achieved direct contact with the deeper bedrock layers. Despite differences between the two sites in soil–bedrock lithological properties, and differences in the woody structure, annual water use by the two forest types was fairly similar. Because stocking density of the Tabor oak forests is strongly related to bedrock characteristics, thinning as a management tool will not change partitioning of the rainfall between different soil pockets, and hence soil water availability to the trees. In contrast, thinning of Kermes oak forests is expected to raise water availability to the remaining trees.     

Lateral Picea shadow effects on Populus tremuloides understory vegetation in central Yukon, Canada

Laterally cast Picea albertiana ssp. albertiana (western white spruce) shadows were analyzed to determine their effect on understory plant abundance in two high-latitude (62.7°N) boreal Populus tremuloides (trembling aspen) forest stands. Each stand had a uniform and continuous overstory, and occurred on level to gently sloping terrain with a submesic moisture regime. Picea >1 m tall had <20% cover in each stand, with few trees equalling or exceeding the height of the P. tremuloides canopy. Understory vegetation composition was sampled in 30-m × 30-m plots that were subdivided into 1.5-m × 1.5-m cells (200 sampled per plot). Picea shadow locations and their areal extent were determined on an hourly basis (7:00-19:00 h Pacific Standard Time on the summer solstice) for individual plot cells using silhouette diagrams constructed from tree height and canopy-related data (n = 140 trees). Shadow data were analyzed using the lower- (Q_L, minimum to first-quartile values) and upper-most (Q_U, third-quartile values to maximum) portions of each species’ abundance distribution. Kruskal-Wallis tests (P < 0.001) indicated that greater Arctostaphylos uva-ursi (bearberry) abundance occurred where shadow cover was the least (daytime average ∼24%); whereas Geocaulon lividum (toadflax), Hylocomium splendens (stairstep moss), and Shepherdia canadensis (buffaloberry) incurred the most shadows (>34% cover) and had the shortest periods of continuous (<6 h) sunlight exposure with <30% Picea shadow cover. Hylocomium and Shepherdia also occurred nearer Picea than Arctostaphylos. Rosa acicularis (wild rose), Linnaea borealis (twinflower), Vaccinium vitis-idaea (bog cranberry), Chamerion angustifolium (fireweed), and Calamagrostis purpurascens (purple reedgrass) incurred intermediate amounts of shadow. Differences in hourly shadow abundance values (Q_U minus Q_L plot cells) were greatest for Arctostaphylos (−14.7%) and Rosa (−10.8%), but H. splendens (+3.8%) and Geocaulon had the least (+1.7%). Greater Hylocomium and Shepherdia abundance occurred in plot cells with more shadow indicating a tolerance for shade, which was contrary to the other species. These differences may represent examples of niche partitioning based on relative light availability. Individual understory species based on percent cover and species richness were more strongly correlated with Picea shadow cover than canopy cover. As a direct representation of impeded light transmittance, assessment of lateral tree shadows may represent a viable approach for investigating within stand compositional variation and temporal change among forest understory species, when a distinct physiognomic difference occurs between seral and climax overstory species.     

Early growth and nutrition of hybrid poplars fertilized at planting in the boreal forest of western Quebec

In order to maximize growth and diagnose nutritional requirements of hybrid poplars (Populus spp.) grown in the boreal forest of western Quebec, the Diagnosis and Recommendation Integrated System (DRIS) was evaluated in conjunction with N:P ratios of trees fertilized at planting. Three hybrid poplar clones (747210; P. balsamifera × trichocarpa, 915005; P. balsamifera × maximowiczii, and 915319; P. maximowiczii × balsamifera) were fertilized with 18 combinations of nitrogen (N), phosphorus (P) and potassium (K). Fertilizers used were granules of ammonium nitrate (34.5-0-0) at 3 levels (0, 20 and 40 g tree⁻¹ of N), triple-superphosphate (0-45-0) at 3 levels (0, 25 and 50 g tree⁻¹ of P), and potassium sulfate (0-0-50) at 2 levels (0, 20 g tree⁻¹ of K). After two growing seasons, P fertilization was the most effective in promoting growth and 25 g tree⁻¹ increased mean stem volume by 41% compared to unfertilized trees. The predictive accuracy of the N:P and DRIS diagnosis methods was generally reliable, however they failed to predict some co-limitations of N and P.     

Fine root production and turnover in forest ecosystems in relation to stand and environmental characteristics

The production and turnover of fine roots (diameter ?2 mm) contributes significantly to carbon cycling in forest ecosystems. We compiled an up-to-date global database covering 186 stands from the literature and estimated fine root production (FRP) and fine root turnover (FRT) for boreal, temperate and tropical forests in order to study the relationships between FRP or FRT and environmental and stand variables. FRP for all plants (trees + understorey) was 311 ± 259 (n = 39), 428 ± 375 (n = 71) and 596 ± 478 g m⁻² a⁻¹ (n = 32) in the boreal, temperate and tropical forests, respectively, and the corresponding annual FRT rates were 0.77 ± 0.70, 1.21 ± 1.04 and 1.44 ± 0.76, respectively. When the FRP and FRT of trees were estimated separately for boreal and temperate forests the differences between the two biomes were insignificant. The mean FRP of trees for the two biomes combined was 306 ± 240 g m⁻² a⁻¹ (n = 86) and the annual FRT was 1.31 ± 1.43. Fine root biomass (FRB) was the most significant factor explaining the variation in FRP, and more so at the tree level than at the stand level, explaining 53% of the variation in FRP for trees at the tree level. The corresponding proportions at the stand level were 21% for all plants and 12% for trees. Latitude, mean annual temperature and annual precipitation each explained <20% of the variation in FRP or FRT. Fine root production and FRT estimates are highly dependent on the species included in the sampling, the sampling depth and the methods used for estimating FRP or calculating FRT. The results indicate that the variation in FRP on a global scale can be explained to a higher degree if we focus on tree roots separately from the roots of the understorey vegetation and on FRP at the tree level instead of FRP at the stand level or on FRT.     

Decomposition of Scots pine fine woody debris in boreal conditions: Implications for estimating carbon pools and fluxes

Litter quality and environmental effects on Scots pine (Pinus sylvestris L.) fine woody debris (FWD) decomposition were examined in three forestry-drained peatlands representing different site types along a climatic gradient from the north boreal (Northern Finland) to south (Southern Finland) and hemiboreal (Central Estonia) conditions. Decomposition (percent mass loss) of FWD with diameter ≤10 mm (twigs) and FWD with diameter >10 mm (branches) was measured using the litter bag method over 1–4-year periods. Overall, decomposition rates increased from north to south, the rate constants (k values) varying from 0.128 to 0.188 year⁻¹ and from 0.066 to 0.127 year⁻¹ for twigs and branches, respectively. On average, twigs had lost 34%, 19% and 19%, and branches 25%, 17% and 11% of their initial mass after 2 years of decomposition at the hemiboreal, south boreal and north boreal sites, respectively. After 4 years at the south boreal site the values were 48% for twigs and 42% for branches. Based on earlier studies, we suggest that the decomposition rates that we determined may be used for estimating Scots pine FWD decomposition in the boreal zone, also in upland forests. Explanatory models accounted for 50.4% and 71.2% of the total variation in FWD decomposition rates when the first two and all years were considered, respectively. The variables most related to FWD decomposition included the initial ash, water extractives and Klason lignin content of litter, and cumulative site precipitation minus potential evapotranspiration. Simulations of inputs and decomposition of Scots pine FWD and needle litter in south boreal conditions over a 60-year period showed that 72 g m⁻² of organic matter from FWD vs. 365 g m⁻² from needles accumulated in the forest floor. The annual inputs varied from 5.7 to 15.6 g m⁻² and from 92 to 152 g m⁻² for FWD and needles, respectively. Each thinning caused an increase in FWD inputs, up to 510 g m⁻², while the needle inputs did not change dramatically. Because the annual FWD inputs were lowered following the thinnings, the overall effect of thinnings on C accumulation from FWD was slightly negative. The contribution of FWD to soil C accumulation, relative to needle litter, seems to be rather minor in boreal Scots pine forests.     

Uncertainty of 21st century growing stocks and GHG balance of forests in British Columbia, Canada resulting from potential climate change impacts on ecosystem processes

Over the coming decades, climate change will increasingly affect forest ecosystem processes, but the future magnitude and direction of these responses is uncertain. We designed 12 scenarios combining possible changes in tree growth rates, decay rates, and area burned by wildfire with forecasts of future harvest to quantify the uncertainty of future (2010-2080), timber growing stock, ecosystem C stock, and greenhouse gas (GHG) balance for 67 million ha of forest in British Columbia, Canada. Each scenario was simulated 100 times with the Carbon Budget Model of the Canadian Forest Sector (CBM-CFS3). Depending on the scenario, timber growing stock over the entire land-base may increase by 14% or decrease by 9% by 2080 (a range of 2.8 billion m³), relative to 2010. However, timber growing stock available for harvest was forecast to decline in all scenarios by 26-62% relative to 2010 (a range of 1.2 billion m³). Forests were an annual GHG source in 2010 due to an ongoing insect outbreak. If half of the C in harvested wood was assumed to be immediately emitted, then 0-95% of simulations returned to annual net sinks by 2040, depending on scenario, and the cumulative (2010-2080) GHG balance ranged from a sink of −4.5 Pg CO₂e (−67 Mg CO₂e ha⁻¹) for the most optimistic scenario, to a source of 4.5 Pg CO₂e (67 Mg CO₂e ha⁻¹) for the most pessimistic. The difference in total ecosystem carbon stocks between the most optimistic and pessimistic scenarios in 2080 was 2.4 Pg C (36 Mg C ha⁻¹), an average difference of 126 Tg CO₂e yr⁻¹ (2 Mg CO₂e yr⁻¹ ha⁻¹) over the 70-year simulation period, approximately double the total reported anthropogenic GHG emissions in British Columbia in 2008. Forests risk having reduced growing stock and being GHG sources under many foreseeable scenarios, thus providing further feedback to climate change. These results indicate the need for continued monitoring of forest responses to climatic and global change, the development of mitigation and adaptation strategies by forest managers, and global efforts to minimize climate change impacts on forests.     

Growth and population structure of the tree species Malouetia tamaquarina (Aubl.) (Apocynaceae) in the central Amazonian floodplain forests and their implication for management

The long-term success of forest management depends primarily on the sustainability of timber production. In this study we analyse the population structure, tree age and wood increment of Malouetia tamaquarina (Aubl.) (Apocynaceae) to define a species-specific minimum logging diameter (MLD) and felling cycle by modelling volume growth. Contrary to other timber species in the nutrient-rich white-water floodplains forests (várzea), M. tamaquarina grows in the subcanopy of old-growth várzea forests. The wood of this species is utilized by local inhabitants in the floodplains for handicraft. In 35 plots of 25 m × 50 m we measured diameter at breast height (DBH) and tree height of all trees taller than 150 cm height. From 37 individuals with DBH > 15 cm we sampled two cores by increment borers to determine the wood density, tree age and diameter increment rates. In the management area of a várzea settlement with about 150 ha recently harvested trees of M. tamaquarina have been recorded and DBH was measured. The species presents an inverse J-shaped diameter distribution indicating that the species is obviously regenerating in the old-growth forests. Tree-ring analysis indicates a mean age of 74.5 years for a DBH of 22.7 cm for a studied population comprising 37 trees with maximum ages of up to 141 years for an individual with a DBH of 45.7 cm. The tree species has low annual diameter increment rates (3.16 ± 0.6 mm) despite a low wood density (0.36 ± 0.05 g cm⁻³). The volume growth model indicates a MLD of 25 cm and a felling cycle of 32.4 years. In the management area 35 trees with a mean DBH of 24 cm were recorded, similar to the defined MLD. The abundance of trees above the MLD is 2.7 trees ha⁻¹, or 405 trees, when extrapolated to the whole management area. Considering a felling cycle of 32.4 years (annual production unit of 4.63 ha) this results in total of 12.5 harvestable trees, almost three times less than actually harvested. The actual practice of harvesting M. tamaquarina risks the overexploitation of this slow-growing species.     

High densities of bell miners Manorina melanophrys associated with reduced diversity of other birds in wet eucalypt forest: Potential for adaptive management

High densities of bell miners (Manorina melanophrys) are known to accelerate dieback in eucalypt forests presumably through their negative impact on other avian insectivores and predatory insects. Some areas of moist eucalypt forest that are managed for sustained timber production also support very high densities of bell miners. In this study, we quantified the relative population density of bell miners in forests, and investigated the relationship between bell miner population density, the relative population density of other birds and species richness. A study site of 900 ha was selected in Olney State Forest on the Central Coast of New South Wales (33°7′ S, 150°22′ E), an area that has been managed for timber production since the 1920s. Monthly census counts were carried out over a 16-month period to include diurnal and seasonal variation. Bell miner population density ranged from 14–38 birds/ha and was found to be negatively correlated with diversity of other species. A linear empirical relationship was found between bird species richness (y) and bell miner relative population density (x) by the equation y = −0.12x + 7.78 (R = 0.9638, n = 8, P < 0.0001), and an increase in bell miner abundance was found to decrease the abundance of other species as given by the equation y = −0.32x + 16.83 (R = −0.9646, n = 8, P < 0.0001).     

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.     

Annual allowable cut for merchantable woody species in a community managed forest in western Kenya

Changes in stand density, basal area, off-take and annual increment were determined from 18 permanent sample plots established in 1997 in Got Ramogi Forest in western Kenya. The plots were assessed in 2003 and 2008. A total of 824 stems ?1.5 m in height were recorded from 43 woody species. Key merchantable woody species comprised 20% of the woody species and 67% of the overall stem density. There was a significant reduction in the overall stand density and in the stem density of key merchantable woody species, but not among other woody species between 1997 and 2008. The basal area decreased significantly among key merchantable woody species, but not for the overall forest. The basal area decreased from 22.6 to 9.7 m² ha⁻¹ for key merchantable woody species. The stand volume of key merchantable woody species decreased from 156 m³ ha⁻¹ in 1997 to 61.7 m³ ha⁻¹ in 2008. The mean annual off-take declined from 10.3 m³ ha⁻¹ year⁻¹ between 1997 and 2003 to 9.1 m³ ha⁻¹ year⁻¹ between 2003 and 2008, while the mean annual increment increased from 2.9 to 3.3 m³ ha⁻¹ year⁻¹. It was predicted that forest recovery would surpass the 1997 stand volume of 156 m³ ha⁻¹ if off-take levels between 10% and 90% of the mean annual increment were adopted. We settled on an annual allowable cut of 80% of the mean annual increment as a compromise between consumptive and conservation interests. We identified over-harvesting as the main cause of the reduction in stem density among key merchantable woody species. A management plan with compartment registers indicating the diversity, abundance and distribution of each woody species was recommended to guide their utilization and monitor their population dynamics.     

Radiation use efficiency in adjacent hardwood and pine forests in the southern Appalachians

The efficiency with which trees convert photosynthetically active radiation (PAR) to biomass has been shown to be consistent within stands of an individual species, which is useful for estimating biomass production and carbon accumulation. However, radiation use efficiency (?) has rarely been measured in mixed-species forests, and it is unclear how species diversity may affect the consistency of ?, particularly across environmental gradients. We compared aboveground net primary productivity (ANPP), intercepted photosynthetically active solar radiation (IPAR), and radiation use efficiency (? = ANPP/IPAR) between a mixed deciduous forest and a 50-year-old white pine (Pinus strobus L.) plantation in the southern Appalachian Mountains. Average ANPP was similar in the deciduous forest (11.5 Mg ha⁻¹ y⁻¹) and pine plantation (10.2 Mg ha⁻¹ y⁻¹), while ? was significantly greater in the deciduous forest (1.25 g MJ⁻¹) than in the white pine plantation (0.63 g MJ⁻¹). Our results demonstrate that late-secondary hardwood forests can attain similar ANPP as mature P. strobus plantations in the southern Appalachians, despite substantially less annual IPAR and mineral-nitrogen availability, suggesting greater resource-use efficiency and potential for long-term carbon accumulation in biomass. Along a 260 m elevation gradient within each forest there was not significant variation in ?. Radiation use efficiency may be stable for specific forest types across a range of environmental conditions in the southern Appalachian Mountains, and thus useful for generating estimates of ANPP at the scale of individual watersheds.     

A comparative analysis of forest cover and catchment water yield relationships in northern China

During the past few decades, China has implemented several large-scale forestation programs that have increased forest cover from 16.0% in the 1980s to 20.4% in 2009. In northern China, water is the most sensitive and limiting ecological factor. Understanding the dynamic interactions between forest ecosystems and water in different regions is essential for maximizing forest ecosystem services. We examined forest cover and runoff relationships in northern China using published data from a variety of sources. In the Loess Plateau region, forest cover is not correlated with annual precipitation (r = 0.08, p > 0.05) at micro (<50 km²) and meso scales (50-1000 km²), while they are positively correlated at macro (>1000 km²) scale (r = 0.77, p < 0.05). Moreover, forest cover is negatively correlated with the runoff coefficient (r = −0.64, p < 0.05). In Northwest China, natural forest distribution is highly correlated with annual precipitation (r = 0.48, p < 0.05) but not with the runoff coefficient (r = −0.09, p > 0.05). In Northeast China, we found a positive relationship between forest cover and the runoff coefficient (r = 0.77, p < 0.05), but the correlation between forest cover and precipitation was not significant (r = 0.28, p > 0.05). The multiple stepwise regression analysis indicated that runoff was influenced by altitude, annual precipitation, forest cover, and PET (potential evapotranspiration) in Northeast China. We concluded that geographic differences could mask the true role of forests in the partitioning of rainfall into runoff and evapotranspiration (ET) in a catchment. In determining the forest-water relationship, one must consider climatic controls on ET in addition to forest cover. Forests could potentially enhance the complementary relationship between ET and PET. Therefore, a greater amount of ET in forested areas may decrease the PET on a regional scale.     

Transpiration and hydraulic traits of old and regrowth eucalypt forest in southwestern Australia

We tested the hypothesis that overstorey of eucalypt forest dominated by tall, large diameter trees uses less water than regrowth stands in the high rainfall zone (>1100 mm year⁻¹) of the northern jarrah (Eucalyptus marginata) forest in southwestern Australia. We measured leaf area, cover, sapwood area and sapwood density at three paired old and regrowth stands. We also measured sapflow velocity at one paired stand (Dwellingup) from June 2007 to October 2008. Old stands had more basal area but less foliage cover, less leaf area and slightly thinner sapwood. The ratio of sapwood area to basal area decreased markedly as tree size increased. Sapwood area of the regrowth forest stands (6.6 ± 0.30 m² ha⁻¹) was nearly double that of the old stands (3.4 ± 0.17 m² ha⁻¹), despite larger basal area at the old stands. Leaf area index of the regrowth stands (2.1 ± 0.26) was only one-third larger than that at the old stands (1.5 ± 0.15); hence, the ratio of leaf area to sapwood area was larger in old stands than in regrowth stands (0.45 ± 0.022 m² cm⁻² versus 0.32 ± 0.045 m² cm⁻²). Our results are consistent with theories that trees have evolved to optimize carbon gain rather than maintain stomatal conductance. Neither sapwood density (540–650 kg m⁻³) nor sap velocity differed greatly between regrowth and old stands. At the old forest site, daily transpiration rose from 0.5 mm day⁻¹ in winter to 0.9 mm day⁻¹ in spring–summer, compared to 0.9 mm day⁻¹ and 1.8 mm day⁻¹ at the regrowth site. Annual water use by the overstorey trees was estimated to be ∼230 mm year⁻¹ for the old stand and ∼500 mm year⁻¹ at the regrowth stand, or 20% and 44% of annual rainfall. The overwhelming role of stand sapwood area in determining stand water use, combined with the marked changes in the ratio of sapwood area to basal area with tree age and size, suggest that stand overstorey structure can be managed to alter overstorey water use and catchment water yield. Silviculture to promote old-forest-like attributes may be a viable means of delivering multiple water and conservation benefits.     

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.