Biomass production and allocation, including fine-root turnover, and annual N uptake in lysimeter-grown basket willows

Annual net primary production (NPP) and N uptake were estimated for lysimeter-grown basket willows (Salix viminalis L.) during 3 years after planting. The willows were grown in a stand structure and continuously supplied with water and liquid fertilizer through drip tubes. The lysimeters contained either clay from the site or washed quartz sand. Shoot growth and leaf litter were measured and fine-root dynamics observed in minirhizotrons. Destructive samples were taken annually in late autumn and entire root systems were washed out. Dry mass and N content of all plant parts were determined. Fine-root production was estimated by two methods, based on destructive samplings and observations in minirhizotrons.

The proportion of biomass allocated below ground increased considerably when estimates based on accumulated NPP were compared with those based on standing dry mass. In the first year, 49 and 58% of annual NPP in willows grown in clay and sand, respectively, was belowground. In subsequent years the proportions were 36–38% and 33–40%. Most belowground production was fine roots. Relatively more N was used belowground in the first year than subsequently, but no substrate-induced differences were observed in the allocation pattern. Both annual NPP and N uptake was always higher in plants in clay than in those in sand: in the final 2 years, 21–22 tonnes DM ha⁻¹ year⁻¹ and 190 kg N ha⁻¹ year⁻¹ in clay, and 9–10 tonnes DM ha⁻¹ year⁻¹ and 100 kg N ha⁻¹ year⁻¹ in sand.     

Nitrogen deposition in Casuarina equisetifolia (Forst.) plantation stands in the dry tropics of Sonbhadra, India

Periodic variations in the concentration, deposition and canopy impact of different forms of N on annual N deposition through rainfall, throughfall and stemflow in 5 and 8 year old stands of Casuarina equisetifolia were studied. Throughfall and stemflow ranged from 70 to 76% and 5–6% of annual precipitation respectively. The total N deposition by rainfall was 11.1 kg ha⁻¹ year⁻¹, and by throughfall was 13.6 kg ha⁻¹ year⁻¹ and 16.5 kg ha⁻¹ year⁻¹ in 5-year-old and 8-year old plantations, respectively. The quantities of N deposited through stemflow in the two plantations were nearly identical, accounting for 1.6 kg ha⁻¹ year⁻¹. Observations of the monthly deposition of NH₄,N, NO₃-N, Kjeldahl-N and organic-N revealed that maximum deposition occurred in July and the minimum in September. Organic-N deposition was 17% less (5-year) than the rainwater content. Net deposition of N, as an effect of canopy, was 7–8.7 kg ha⁻¹ year⁻¹, which was added directly to the available nutrient pool of soil.     

Biomass distribution and productivity ofPinus edulis—Juniperus monosperma woodlands of north-central Arizona

Above-ground biomass distribution, leaf area, above-ground net primary productivity and foliage characteristics were determined for 90- and 350-year-oldPinus edulis-Juniperus monosperma ecosystems on the Colorado Plateau of northern Arizona. These ecosystems have low biomass, leaf area and primary productivity compared with forests in wetter environments. Biomass of the 350-year-old pinyon-juniper stand examined in this study was 54.1 mg ha⁻¹; that of the 90-year-old stand was 23.7 mg ha⁻¹. Above-ground net primary production averaged 2.12 mg ha⁻¹ year⁻¹ for the young and 2.88 mg ha⁻¹ year⁻¹ for the mature stand; tree production was about 80% of these values for both stands. Projected ecosystem leaf area (LAI) of the stands was 1.72 m² m⁻² and 1.85 m² m⁻², respectively. Production efficiency (dry matter production per unit leaf area) was 0.129 kg m⁻² year⁻¹ for the young, and 0.160 kg m⁻² year⁻¹ for the mature stand. Production efficiency of the study sites was below the 0.188 kg m⁻² year⁻¹ reported for xeric, pure juniper stands in the northern Great Basin. Biomass of pinyon-juniper ecosystems of northern Arizona is generally below the 60–121 mg ha⁻¹ reported for pinyon-juniper stands of the western Great Basin in Nevada. A climatic gradient with summer precipitation decreasing between southeast Arizona and northwest Nevada occurs in the pinyon-juniper region. Great Basin pinyon-juniper ecosystems lie at the dry-summer end of this gradient while pinyon-juniper ecosystems of the Colorado Plateau lie at about the middle of this gradient. In spite of wetter summers, pinyon-juniper ecosystems of northern Arizona are less productive than those of the Great Basin.     

Nitrogen-fertilization impacts on carbon sequestration and flux in managed coastal Douglas-fir stands of the Pacific Northwest

We examined whether N-fertilization and soil origin of Douglas-fir [Psuedotsuga menziesii (Mirb.) Franco] stands in western Washington state could affect C sequestration in both the tree biomass and in soils, as well as the flux of dissolved organic carbon (DOC) through the soil profile. This study utilized four forest sites that were initially established between 1972 and 1980 as part of Regional Forest Nutrition Research Project (RFNRP). Two of the soils were derived from coarse-textured glacial outwash and two from finer-textured volcanic-source material, primarily tephra, both common soil types for forestry in the region. Between 1972 and 1996 fertilized sites received either three or four additions of 224 kg N ha⁻¹ as urea (672–896 kg N ha⁻¹ total). Due to enhanced tree growth, the N-fertilized sites (161 Mg C ha⁻¹) had an average of 20% more C in the tree biomass compared to unfertilized sites (135 Mg C ha⁻¹). Overall, N-fertilized soils (260 Mg C ha⁻¹) had 48% more soil C compared to unfertilized soils (175 Mg C ha⁻¹). The finer-textured volcanic-origin soils (348 Mg C ha⁻¹) had 299% more C than glacial outwash soils (87.2 Mg C ha⁻¹), independent of N-fertilization. Soil-solution DOC collected by lysimeters also appeared to be higher in N-fertilized, upper soil horizons compared to unfertilized controls but it was unclear what fraction of the difference was lost from decomposition or contributed to deep-profile soil C by leaching and adsorption. When soil, understory vegetation and live-tree C compartments are pooled and compared by treatment, N-fertilized plots had an average of 110 Mg C ha⁻¹ more than unfertilized controls. These results indicate these sites generally responded to N-fertilization with increased C sequestration, but differences in stand and soil response to N-fertilization might be partially explained by soil origin and texture.     

An empirical cohort model for management of Terra Firme forests in the Brazilian Amazon

A model to project forest growth in the Terra Firme forests of the eastern Amazon is described. It is based on 12–17 years measurements from experimental plots at Jarí and Tapajós. Forest stands are represented by cohorts of species group, diameter, and defect. There are 54 species groups, with a robust diameter increment function fitted to each, tables of mortality by crown and defect status, and recruit lists by disturbance level and locality. Stand level functions partition trees by crown status, and modify growth for stand density. Recruitment is a function of basal-area losses. Evaluation compares model performance with two experiments involving heavy felling in Tapajos State Forest. At one site, total bole volume growth of all species over 45 cm DBH was 2.56 m³ ha⁻¹ year⁻¹ over 17 years, whereas the model projected 3.13 m³ ha⁻¹ year⁻¹. At the other site, actual growth over 12 years was 0.39 m³ ha⁻¹ year⁻¹, with the model giving an identical result. Both felled and control plots are compared in the study and accurately simulated. Some weaknesses in the model are discussed.     

Nutrient accumulation and role of atmospheric deposition in coniferous stands

Three stand types on drained wetlands, all 31 years old, were studied. The stands were: (1) Scots pine, unfertilized; (2) Scots pine, fertilized; and (3) Norway spruce, fertilized. Amounts of nutrients (N, K, Ca, Mg, P, S, B, Fe, Mn, Zn, Cu) in above-ground biomass for all three stand types could be simulated precisely by a curvilinear regression model, with stand volume on bark as regressor. Net H⁺ production of the fertilized pine was estimated to be 661 mol H⁺ ha⁻¹ year⁻¹ from establishment to 31 years of age. The corresponding value for spruce was 1232 mol H⁺ ha⁻¹ year⁻¹. Atmospheric inputs to the pine and spruce sites were 695 and 516 mol H⁺ ha⁻¹ year⁻¹, respectively. Atmospheric input of N was 2.3 and 1.3 times the accumulation in the biomass of unfertilized and fertilized pine, whereas the value for spruce was 0.7. The corresponding ratios for S were 43, 19, and 11.     

Some nutrient dynamics associated with litterfall and litter decomposition in hoop pine plantations of southeast Queensland, Australia

Litterfall was collected over a 12-month period with littertraps in hoop pine (Araucaria cunninghamii) plantations aged 10, 14 and 62 years in southeast Queensland, Australia. The bulk of litterfall occurred during spring, mainly as hoop pine foliage with the annual litterfall ranging between 6.0 and 10.9 t ha⁻¹, respectively, for the younger stands (10 and 14 years) and the mature 62-year old stand. The amount of nitrogen (N) and phosphorous (P) recycled annually through litterfall was lower in the younger stands (28–37 kg N ha⁻¹ and 4.4–5.3 kg P ha⁻¹) compared with that of the mature stand (85 N ha⁻¹ and 6.2 kg P ha⁻¹). The N and P retranslocated during senescence varied across the three stands studied with a trend for N and P retranslocation to increase as availability of soil mineral-N decreased.

Decomposition of the hoop pine foliage component of litter was also studied in the same stands using a litterbag technique and mass-balance analysis. The estimated half-life of hoop pine foliage mass ranged between 1.5 and 1.8 years. Litter-mass loss was strongly correlated with litter substrate quality indicators of N, C, P, C/N ratio, lignin, lignin/N ratio and polyphenols. During the course of the study, there was no difference in litter-mass loss between the stands of different ages. During the 15-month period, the order of element release from the hoop pine litter was K>Na>C>Mg>P, with N, Ca and Mn generally demonstrating varying degrees of net accumulation. During the course of the study, the lignin/C ratio of the hoop pine litter increased from 0.61 to 0.96. This suggested that the litter-C was predominantly in a recalcitrant form and, therefore, the associated N was unlikely to be rapidly released in the hoop pine litter layer.     

Nutrient cycling in a clonal stand of Eucalyptus and an adjacent savanna ecosystem in Congo: 3. Input–output budgets and consequences for the sustainability of the plantations

Clonal plantations of Eucalyptus have been introduced since 1978 on savanna soils of the coastal plains of Congo. Atmospheric deposition, canopy exchange and transfer through the soil were estimated on the whole rooting depth (6 m) over 3 years, in an experimental design installed in a native savanna and an adjacent 6-year-old Eucalyptus plantation. Complementary measurements after planting the experimental savanna made it possible to establish input–output budgets of nutrients for the whole Eucalyptus rotation and to compare them with the native savanna ecosystem.

In this highly-weathered soil, atmospheric deposits and symbiotic N fixation by a legume species balanced the nutrient budgets in savanna, despite large losses during annual burnings. After afforestation, weeding in the Eucalyptus stands eliminated the leguminous species responsible for a N input by symbiotic fixation of about 20 kg ha⁻¹ year⁻¹. Whereas the budgets of P, K, Ca and Mg were roughly balanced, the current silviculture led to a deficit of about 140 kg N ha⁻¹ in the soil, throughout a 7-year rotation. This deficit was large relative to the pool of total N in the upper soil layer (0–50 cm), which was about 2 t ha⁻¹. Therefore, the sustainability of Congolese plantations will require an increase in N fertilizer inputs over successive rotations to balance the N budget. These results were consistent with field trials of fertilization. Practical consequences of these budgets were identified, in order to: (i) direct field trials of fertilization, (ii) select appropriate methods of soil preparation, weed control and harvest, (iii) highlight the importance of fire prevention in this area, and (iv) support the implementation of field trials aiming at introducing a biological nitrogen fixing understorey in Eucalyptus stands.     

Use of a gradient of N-deposition to calculate effect-related soil and vegetation measures in deciduous forests

Deposition of N and S has increased since the 1950s in most European countries and N accumulates in ecosystems that are not N saturated. This study shows long-term effects of a (modelled) N deposition of 7–17 kg N ha⁻¹ per year on biological and chemical processes in soil, vegetation composition, and functional types of field-layer plant species in deciduous forests. Soil pH largely determined the response of the soil processes, emphasising the importance to compare soils of similar acidity regarding the effects of N deposition. The most pronounced effects were demonstrated for the most acid study plots. When we compared regions with a deposition of 7 and 17 kg N ha⁻¹ per year we found a 40–80% higher soil N mineralisation rate, 2–90% higher nitrification rate and 10–25% lower C:N ratio in the region with the highest deposition. Similar but smaller differences were indicated when regions with a deposition of 7 and 10 kg N ha⁻¹ per year were compared. Number of species was lower in the regions with the highest deposition. Literature data for plants on N concentration, nitrate reductase activity (NRA), growth rates, morphology and height were calculated on a site basis. They varied to different extent between the regions. The N concentration was 7–24% higher in the regions with the highest N deposition. We argue that the effect-related critical load based on our results should be set to a N deposition of 7–10 kg N ha⁻¹ per year. Critical loads for a subdivision of deciduous forests would give lower critical loads for the most acid soils compared to less acid soil.     

Clear-cutting reduces nitrate leaching in a pine plantation of high natural N status

Following the tree harvest, the biogeochemistry of a catchment is modified by changes in soil temperature and moisture, and nutrient cycling. We monitored soil-solution and stream-water chemistry, and soil properties in a Pinus radiata D. Don plantation in New Zealand before and after clear-cutting and replanting in 1997. The annual rainfall during the study was 1440–1860 mm. The soil was a 1800-year-old pumice soil of high natural N status; the catchment had received large inputs of volcanic N in rain, probably over the 1800 years since the pumice had been deposited. The leaching loss of nitrate-N was 28 kg ha⁻¹ yr⁻¹ in 1996, and then decreased sharply after clear-cutting to 3 kg ha⁻¹ yr⁻¹ in 1998 and <1 kg ha⁻¹ yr⁻¹ in 1999. Weed growth and soil microbial biomass increased during this time, and would have removed much of the N from soil solution in the upper soil layers. Although the catchment was small (8.7 ha), there was a 2-year lag until N decreased in stream-water; the losses of dissolved organic N to stream-water were low. There was no change in soil pH over the 4 years, but spring-water pH appeared to increase, which was consistent with the increase in bicarbonate that accompanied grass/weed growth. The export of cations (mmol_c l⁻¹) in the spring-water was Na>Ca>Mg=K as expected for rhyolitic pumice, and the total concentration was probably controlled by the accompanying anions. The export of anions was NO₃=Cl>SO₄=HCO₃ before harvest and HCO₃=Cl>SO₄=NO₃ after harvest.     

Effects of intensive harvesting on nutrient capitals of three forest types in New England

Effects of whole-tree clearcutting are being studied in three major forest types in the northeastern United States: a spruce-fir forest in central Maine, a northern hardwood forest in New Hampshire, and a central hardwood forest in Connecticut. At each site we sampled total and extractable nutrient capitals, inputs and outputs of nutrient ions in precipitation and streamflow, nutrient removals in harvested products, and nutrient accumulation in regrowth. Depending upon location, combined losses of nutrients in harvested products and increased leaching to streams were in the ranges of 374–558 kg ha⁻¹ for Ca, 135–253 kg ha⁻¹ for K, 50–65 kg ha⁻¹ for Mg, 248–379 kg ha⁻¹ for N, and 19–54 kg ha⁻¹ for P. Opportunities for replacing these losses over the next rotation are best for N. Data on inputs in precipitation versus outputs in streamflow indicate that, once effects of harvest subside, most N in precipitation will stay within the forest. By contrast, Ca shows a net output of 8–15 kg ha⁻¹ year⁻¹ from uncut watersheds, and the added leaching losses due to harvest may have a serious impact on Ca capital. This is especially the case for the Connecticut site, where total site capital for Ca is only about 4000 kg ha⁻¹.     

Stand growth scenarios for Tectona grandis plantations in Costa Rica

Management scenarios with rotation lengths of 20 and 30 years were developed for different site qualities (high, medium and low) under two different management options (high individual tree growth versus high stand growth) for teak (Tectona grandis L.f.) in Costa Rica. The scenarios are based on data collected in different regions in Costa Rica, representing different site conditions, offering a variety of possible management options for high-quality teak yield.

Three competition indices were used for modeling the competition and for the definition of intensities and the plantation age at thinning. The maximum site occupation (MSO) and the Reineke density index (RDI) provide conservative stand density management limits, resulting in the need to execute several thinning frequently. The competition factor (CF) matches the field observations and seems to be more appropriate for the growth characteristics of the species.

Final stand densities varied between 120 and 447 trees ha⁻¹, with mean diameter at breast height (dbh) of 24.9–47.8 cm, and mean total heights between 23.0 and 32.4 m, depending on rotation length and site quality. The mean annual increment of total volume (MAI_Vol) at the end of the rotation varied from 11.3 to 24.9 m³ ha⁻¹ year⁻¹, accumulating a total volume over rotation of 268–524 m³ ha⁻¹.

The most suitable scenario for teak plantations for high-quality sites is the 30-year-rotation scenario with five thinnings of intensities between 20 and 50% (of the standing trees) at the ages of 4, 8, 12, 18 and 24 years. After the sectioning of the merchantable stem in 4-m length logs, the merchantable volume varied between 145 and 386 m³ ha⁻¹, with an estimated heartwood volume of 45–195 m³ ha⁻¹, both depending on rotation length and site quality.     

Variation in the amount and quality of litterfall in a Pinus sylvestris L. stand growing on a bog

The amount and nutrient content of the above-ground litterfall was followed for 9 years in an unfertilized, PKMgB and NPKMgB fertilized Scots pine stand growing on a drained ombrotrophic bog in eastern Finland. The annual litterfall on unfertilized plots was 1995 kg ha⁻¹, of which needles accounted for 74%. The effective temperature sum (threshold value + 5°C) explained 99% of the annual variation in the amount of needle litterfall when the data from one atypical year were excluded from the analysis. Nutrient concentrations were, except for Fe, higher in needle litter than in the other litterfall fractions. Nitrogen, P and K concentrations were low in autumn, and those of Ca and Mn high, possibly owing to variation in the mobility of elements during senescence. The annual litterfall input of N to the soil was 12.4 kg ha⁻¹, and the corresponding values for P and K were 0.08 kg ha⁻¹ and 1.81 kg ha⁻¹, respectively. Fertilization reduced needle litterfall in the first year after treatment, but had no effect thereafter. The amount of other litterfall fractions was not affected by fertilization in any of the 9 years of the study. Nitrogen, P, K and B concentrations increased in the needle litter after both fertilization treatments. The results indicate long-term cycling of fertilizer nutrients on the site.     

Modelling the yield of Pinus radiata on a site limited by water and nitrogen

A process-based model is described and applied to a range of Pinus radiata D. Don stands, aged 9–12 years, growing on stabilised sand dunes in a stocking × fertiliser experiment in Woodhill State Forest, New Zealand. The model requires inputs of daily weather data (maximum and minimum air temperatures and rainfall), physical characteristics of the site (longitude, latitude, rootzone depth and relationship between root-zone soil matric potential and volumetric water-content) and crop (stocking, crown dimensions and leaf-area index) and crop physiological parameters (e.g., maximum stomatal conductance). The model was used to simulate components of the forest water-balance and annual net photosynthesis for a defined crop canopy architecture. Simulated daily root-zone water storage in both open and closed canopy stands generally agreed with monthly measurements made over a complete year. Simulated net annual photosynthesis ranged from 23 to 33 t C ha⁻¹ year⁻¹ and comparison with measured stem-volume increments of 12–38 m³ ha⁻¹ year⁻¹ over the same time periods resulted in a strong positive correlation. Ratios of stem-volume increment to net photosynthesis suggested that fertilised and unfertilised stands had a 26 and 14%, respetively, allocation of C to stem growth. Simulations using weather data for a dry year with 941 mm year⁻¹ rainfall indicated that annual net photosynthesis and transpiration of fully stocked stands were reduced by 41 and 45%, respectively, compared to those in a wet year with 153 mm year⁻¹ rainfall. Operational applications of the model to forest management in quantifying environmental requirements for stand growth and examining silvicultural alternatives are discussed.     

Fate of N-labelled nitrate in a wet summer under different residue management regimes in young hoop pine plantations

A field study was conducted to investigate the fate of ¹⁵N-labelled nitrate applied at 20 kg N ha⁻¹ in a wet summer to microplots installed in areas under different residue management regimes in second-rotation hoop pine (Araucaria cunninghamii) plantations aged 1–3 years in south-east Queensland, Australia. PVC microplots of 235 mm diameter and 300 mm long were driven into 250 mm soil. There were three replications of each of eight treatments. These were areas just under and between 1-year-old windrows (ca. 2–3 m in width) of harvesting residues spaced 15 m apart, and with and without incorporated foliage residues (20 t DM ha⁻¹); the areas just under and between 2- or 3-year-old windrows spaced 10 m apart. Only 7–29% of the added ¹⁵N was recovered from the top 750 mm of the soil profile with the leaching loss estimated to be 70–86% over the 34-day period. The ¹⁵N loss via denitrification was 3.7–6.3% by directly measuring the ¹⁵N gases emitted. The microplots with the incorporated residues at the 1-year-old site had the highest ¹⁵N loss (6.3%) as compared with the other treatments. The ¹⁵N mass balance method together with the use of bromide (Br) tracer applied at 100 kg Br ha⁻¹ failed to obtain a reliable estimate of the denitrification loss. The microplots at the 1-year-old site had higher ¹⁵N immobilisation rate (7.5–24.7%) compared with those at 2- and 3-year-old sites (2.1–3.6%). Incorporating the residues resulted in an increase in ¹⁵N immobilisation rate (24.5–24.7%) compared with the control without the incorporated residues (8.4–14.3%). These findings suggest that climatic conditions played important roles in controlling the ¹⁵N transformations in the wet summer season and that the residue management regimes could also significantly influence the ¹⁵N transformations. Most of the ¹⁵N loss occurred through leaching, but a considerable amount of the ¹⁵N was lost through denitrification. Bromide proved to be an unsuitable tracer for monitoring the ¹⁵N leaching and movement under the wet summer conditions.     

Long-term base cation mass balances for Swedish forests and the concept of sustainability

Data from the Swedish Forest Inventory was used to calculate mass balances for base cations Ca, Mg and K for Swedish forests. Using lysimeter and forest survey soil analyses to estimate present base cation leaching from the root zone reveals that weathering plus base cation deposition is not sufficient to support both, the present base cation leaching rate and the present rate of uptake caused by stem growth. Calculations suggest that 96% of the productive forested area may have higher rates of removal than supply for one or more base cation. Under a best-case scenario, assuming less pollution, the present growth rate and 100% efficiency in uptake of available nutrients, the area with more removal than supply would still be at least 30% of the total area. Forest soils are being depleted at a rate where the exchangeable reservoirs have high risk of being severely depleted in the next few decades in central and southern Sweden. During 1983–1985 the depletion rate is calculated to be, on the average, 0.33 keq ha⁻¹ year⁻¹. The weathering rate and present base cation deposition can sustain growth at a level where (80–85)×10⁶m³ stemwood year⁻¹ can be harvested. Any harvested growth beyond this volume must be sustained by artificial means.

For whole-tree harvesting without base cation return, the calculations indicate that it would significantly increase the base saturation depletion rate to an average of 0.62 keq ha⁻¹ year⁻¹, and risk depletion of the soil in less than one-to-two rotation periods almost anywhere in Sweden.

The calculations stress the importance that sustainable forest management must include the management of nutrient fluxes and reservoirs.     

Carbon uptake by secondary forests in Brazilian Amazonia

Estimating the contribution of deforestation to greenhouse gas emissions requires calculations of the uptake of carbon by the vegetation that replaces the forest, as well as the emissions from burning and decay of forest biomass and from altered emissions and uptakes by the soil. The role of regeneration in offsetting emissions from deforestation in the Brazilian Legal Amazon has sometimes been exaggerated. Unlike many other tropical areas, cattle pasture (rather than shifting cultivation) usually replaces forest in Brazilian Amazonia. Degraded cattle pastures regenerate secondary forests more slowly than do fallows in shifting cultivation systems, leading to lower uptake of carbon. The calculations presented here indicate that in 1990 the 410 × 10³ km² deforested landscape was taking up 29 × 10⁶ t of carbon (C) annually (0.7 t C ha⁻¹ year⁻¹). This does not include the emissions from clearing of secondary forests, which in 1990 released an estimated 27 × 10⁶ t C, almost completely offsetting the uptake from the landscape. Were the present land-use change processes to continue, carbon uptake would rise to 365 × 10⁶ t annually (0.9 t C ha⁻¹ year⁻¹) in 2090 in the 3.9 × 10⁶ km⁶ area that would have been deforested by that year. The 1990 rate of emissions from deforestation in the region greatly exceeded the uptake from regrowth of replacement vegetation.     

Pre-commercial thinning effects on growth, yield and mortality in even-aged paper birch stands in British Columbia

The aim of this study was to quantify 5-year growth, yield and mortality responses of 9- to 13-year-old naturally regenerated, even-aged paper birch (Betula papyrifera Marsh.) stands to pre-commercial thinning in interior British Columbia. The study included four residual densities (9902–21,807 stems ha⁻¹ (unthinned control), 3000, 1000 and 400 stems ha⁻¹) and four sites with 3-fold within-site replication in a randomised block design. The largest, straightest, undamaged trees were selected to leave during thinning. Thinning reduced stand basal area from 5.90 m² ha⁻¹ in the control to 2.50, 1.53 and 0.85 m² ha⁻¹ in the three thinning treatments, representing 42, 26 and 15% of control basal area, respectively. After 5 years, total stand volume per plot remained lower in the three thinning treatments than the control (50.20, 30.07, 18.99 and 11.86 m³ in the control, 3000, 1000 and 400 stems ha⁻¹ treatments), whereas mean stand diameter, diameter increment, height, and height increment were increased by thinning, and top height (tallest 100 trees ha⁻¹) was unaffected. When a select group of crop trees (largest 250 trees ha⁻¹) in the thinning treatments was compared with the equivalent group in the control, there was a significant increase in mean diameter, diameter increment, basal area, basal area increment, and volume increment. Mean height, height increment, top height, and total volume were unaffected by thinning. Crop tree diameter increment was the greatest following thinning to 400 stems ha⁻¹ for all diameter classes. Thinning to 1000 stems ha⁻¹ resulted in lower diameter increment than thinning to 400 stems ha⁻¹ but tended to have higher volume increment. Dominant trees responded similarly to subdominant trees at 400 stems ha⁻¹, but showed the greatest response at 3000 stems ha⁻¹. Results suggest that pre-commercial thinning of 9–13-year-old stands to 1000 stems ha⁻¹ would improve growth of individual trees without seriously under-utilising site resources.     

Biomass and carbon sequestration of ponderosa pine plantations and native cypress forests in northwest Patagonia

Fast growth tree plantations and secondary forests are considered highly efficient carbon sinks. In northwest Patagonia, more than 2 million ha of rangelands are suitable for forestry, and tree plantation or native forest restoration could largely contribute to climate change mitigation. The commonest baseline is the heavily grazed gramineous steppe of Festuca pallescens (St. Yves) Parodi. To assess the carbon sequestration potential of ponderosa pine (Pinus ponderosa (Dougl.) Laws) plantations and native cypress (Austrocedrus chilensis (Don) Flor. et Boutl.), individual above and below ground biomass models were developed, and scaled to stand level in forests between 600 and 1500 annual rainfall. To calculate the carbon sequestration baseline, the pasture biomass was simulated. Also, soil carbon at two depths was assessed in paired pine-cypress-pasture sample plots, the same as the litter carbon content of both forest types. Individual stem, foliage, branch and root log linear equations adjusted for pine and cypress trees presented similar slopes (P>0.05), although some differed in the elevations. Biomass carbon was 52.3 Mg ha⁻¹ (S.D.=30.6) for pine stands and 73.2 Mg ha⁻¹ (S.D.=95.4) for cypress forests, given stand volumes of 148.1 and 168.4 m³ ha⁻¹, respectively. Soil carbon (litter included) was 86.3 Mg ha⁻¹ (S.D.=46.5) for pine stands and 116.5 Mg ha⁻¹ (S.D.=38.5) for cypress. Root/shoot ratio was 19.5 and 11.4%, respectively. The low r/s value for cypress may account for differences in nutrient cycling and water uptake potential. At stand level, differences in foliage, taproot and soil carbon compartments were highly significative (P<0.01) between both forest types. In pine stands, both biomass and soil carbon were highly explained by the rainfall gradient (r²=0.94). Nevertheless, such a relationship was not found for cypress, possibly due to stand and soil disturbances in sample plots. The carbon baseline estimated in pasture biomass, including litter, was 2.6 Mg ha⁻¹ (S.D.=0.8). Since no differences in soil carbon were found between pasture and both forest types, additionality should be accounted only by biomass. However, the replacement of pasture by pine plantations may decrease the soil carbon storage, at least during the first years. On the other hand, the soil may be a more relevant compartment of sequestered carbon in cypress forests, and if pine plantation replaces cypress forests, soil carbon losses could cause a negative balance.     

Estimation of shoot biomass productivity in Estonian Salix plantations

Shoot biomass production was estimated in two Estonian short rotation forest (SRF) plantations during the first rotation cycle (1994–1997). The plantations were established with six clones of Salix viminalis and one clone of Salix dasyclados in 1993. The plantation, located on well-composed organic soil, was characterised by higher productivity (6.2 t DM ha⁻¹ per year) compared with the plantation on poor mineral soil (5.2 t DM ha⁻¹ per year). Fertilisation of the latter plantation increased its productivity to 11.0 t DM ha⁻¹ per year, which is the value close to a predicted maximum for Swedish climatic conditions. In fertilised plots, clone 81090 of S. dasyclados was characterised by the highest productivity among all clones, but also by high stool mortality. Clones 78021 and 78183 of S. viminalis had the most stable and relatively high productivity and can therefore be recommended as promising planting material for SRF in Estonia.

When estimating production, the use of proper allometric relations between shoot dry weight and diameter is of crucial importance. Additional measurements on 1-year-old shoots in 1998 showed that besides shoot age also clone and fertilisation are significant factors influencing allometric relations. The dry weight of fertilised shoots was about 10% lower than that of non-fertilised shoots of the same height and diameter. Older shoots were heavier than younger shoots with a similar diameter.