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.     

Water/nutrient interactions affecting the productivity of stands of Pinus radiata

The accumulation of above-ground biomass and the seasonal patterns of leaf-area development, foliar nutrient concentrations and tree and soil water-status have been measured for fertilised, irrigated, and control stands of Pinus radiata D. Don growing on a low-productivity site, average annual precipitation of 790 mm, near Canberra in southeastern Australia. In the second growing-season after treatments commenced, projected leaf-area index reached peak values of 7 on the irrigated/fertilised stands compared with approximately 5 on the other stands. Average canopy nitrogen concentration (dry-weight basis) varied across the treatments from 9 to 17 mg g⁻¹. Measurements of soil and tree water-status over a 2-year period indicated that stands which were not irrigated experienced summer droughts of up to 4 months duration.

Annual volume production measured over the 2-year period ranged from 17 to 45 m³ ha⁻¹. The extent to which this variation could be attributed to differences in leaf area, rats of photosynthesis, duration of the period of positive net photosynthesis, and hence growth, was analysed in terms of a process-based model of stand growth dependent on climate and soil water-balance.

Annual canopy net photosynthesis simulated by the model ranged from 18 t carbon ha⁻¹ for the control stand to 38 t ha⁻¹ for the irrigated/fertilised stands. Simulations indicated that 67% of this difference could be attributed to the role of irrigation in extending the period of active growth. The additional leaf area carried by the irrigated/fertilised stands contributed a further 23%, while differences in rates of photosynthesis, related to nitrogen nutrition, explained the remaining 10%.     

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.     

Estimation of litter fall and seed production of Acacia mangium in a forest plantation in South Sumatra, Indonesia

Annual litter fall of Acacia mangium in the period of September 1995 to August 1996 was estimated at 5939 kg ha⁻¹ year⁻¹ and from September 1995 to August 1996 at 6048 kg ha⁻¹ year⁻¹, with the highest seasonal production in the dry season. The litter fall was dominated mainly by leaves, 4446 kg (75%) and 4137 kg (68%), respectively. Seed production in the litter fall was estimated at 42.4 kg ha⁻¹ year⁻¹ (4.1 million seeds ha⁻¹) and 39 kg ha⁻¹ year⁻¹ (3.8 million seeds ha⁻¹), with the highest in the dry season from June to October. The accumulated litter fall in the forest floor together with shrubs and grass provide a high fuel load, increasing fire risk.     

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.     

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.     

Deposition of atmospheric constituents and its impact on nutrient budgets of oak forests (Quercus petraea and Quercus robur) in Lower Austria

Geochemical processes in central European oak ecosystems (Quercus petraea and Quercus robur) suffering stand decline were studied in two oak stands of the Weinviertel, Lower Austria, about 30 km north of Vienna. Stores of chemical elements were determined by soil and biomass inventories. Deposition input was monitored over a 2 year period by bulk sampling of throughfall. Soil solution chemistry was studied by tension lysimetry over a 1 year period. Mineral nutrition of oak was judged by foliar analysis. Bulk deposition rates were 10–12 kg N ha⁻¹ year⁻¹, and 15–20 kg S ha⁻¹ year⁻¹. Total annual nitrogen gain is high. Both systems lose calcium and magnesium. Foliar nutrient levels indicate sufficient nutrition with main mineral nutrients, except for magnesium, which is in moderately low supply. Based on these findings, the hypothesis that pollutant deposition has been the cause of a sudden and severe appearance of decline symptoms in the second half of the 1980s must be dismissed. The data on deposition rates and ecosystem nutrient status, however, indicate that the soil of both systems is acidifying, nitrogen stores are increasing, and magnesium pools are depleted. If deposition of pollutants continues at current rates, a slow but steady degradation of many oak ecosystems in the Austrian Weinviertel is inevitable.     

Dynamics and potentials of carbon sequestration in managed stands and wood products in Finland under changing climatic conditions

Carbon (C) sequestration was studied in managed boreal forest stands and in wood products under current and changing climate in Finland. The C flows were simulated with a gap-type forest model interfaced with a wood product model. Sites in the simulations represented medium fertile southern and northern Finland sites, and stands were pure Scots pine and Norway spruce stands or mixtures of silver and pubescent birch.

Changing climate increased C sequestration clearly in northern Finland, but in southern Finland sequestration even decreased. Temperature is currently the major factor limiting tree growth in northern Finland. In southern Finland, the total average C balance over the 150 year period increased slightly in Scots pine stands and wood products, from 0.78 Mg C ha⁻¹ per year to 0.84 Mg C ha⁻¹ per year, while in birch stands and wood products the increase was larger, from 0.64 Mg C ha⁻¹ per year to 0.92 Mg C ha⁻¹ per year. In Norway spruce stands and wood products, the total average balance decreased substantially, from 0.96 Mg C ha⁻¹ per year to 0.32 Mg C ha⁻¹ per year. In northern Finland, the total average C balance of the 150 year period increased under changing climate, regardless of tree species: in Scots pine stands and wood products from 1.10 Mg C ha⁻¹ per year to 1.42 Mg C ha⁻¹ per year, in Norway spruce stands and wood products from 0.69 Mg C ha⁻¹ per year to 0.99 Mg C ha⁻¹ per year, and in birch stands and wood products from 0.43 Mg C ha⁻¹ per year to 0.60 Mg C ha⁻¹ per year.

C sequestration in unmanaged stands was larger than in managed systems, regardless of climate. However, wood products should be included in C sequestration assessments since 12–55% of the total 45–214 Mg C ha⁻¹ after 150 years' simulation was in products, depending on tree species, climate and location. The largest C flow from managed system back into the atmosphere was from litter, 36–47% of the total flow, from vegetation 22–32%, from soil organic matter 25–30%. Emissions from the production process and burning of discarded products were 1–6% of the total flow, and emissions from landfills less than 1%.     

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.     

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.     

Nitrogen mineralization in irrigated plantations of shisham and mulberry

Ammonification and nitrification rates and nitrogen uptake were measured using the buried-bag technique in irrigated mixed plantations of shisham (Dalbergia sissoo Roxb. ex DC.) and mulberry (Morus alba L.). Nitrogen transformations were rapid in these stands, particularly following thinning to reduce stand density. In young stands, net N mineralization was 26.72 mg N kg⁻¹ soil month⁻¹ (approximately 480 kg ha⁻¹ month⁻¹), but, as the end of the 22-year rotation approached, nitrification slowed to 13.41 mg N kg⁻¹ soil month⁻¹ (approximately 241 kg ha⁻¹ month⁻¹). N₂-fixing shisham appeared to respond after thinning only to the increased space and temporarily reduced competition for light and moisture, but mulberry appeared to benefit greatly from the nitrogen released through mineralization following thinning.     

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.     

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.     

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.     

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.     

Growth, biomass production and nutrient accumulation by seven tree species irrigated with municipal effluent at Wodonga, Australia

In the Murray-Darling basin, irrigation of tree crops is being evaluated as an alternative method for the disposal of municipal effluent. A study was carried out at Wodonga in which seven tree species were irrigated with effluent for a period of 4 years. Irrigation was calculated weekly on the basis of pan evaporation and rainfall during the preceding week. Annual irrigation varied between 1190 mm and 1750 mm with a total input over the 4-year-period of 4940 mm.

Height and diameter growth varied significantly between species. At age 4, mean dominant height of Eucalyptus grandis, E. saligna and Populus deltoides × P. nigra ranged from 14.3 to 15.0 m compared with 6.6 to 9.8 m for Casuarina cunninghamiana, E. camaldulensis, P. deltoides and Pinus radiata. Wood production of the faster-growing species (E. grandis and E. saligna) was approximately 130 m³ ha⁻¹, or around 32 m³ ha⁻¹ year⁻¹ over a 4-year period. This was nearly three-fold the production of the other native species and twice that of Pi. radiata. Volume growth of P. deltoides × P. nigra (85 m³ ha⁻¹) was significantly greater than that of P. deltoides (42 m³ ha⁻¹).

Accumulation of nutrients in the above-ground biomass varied significantly between species and ranged from 24 to 41 g m⁻² for N, 2.6 to 5.9 g m⁻² for P, 0.5 to 9.2 g m⁻² for Na, 12 to 27 g m⁻² for K, 7 to 52 g m⁻² for Ca and 3.1 to 7.9 g m⁻² for Mg. Nutrient accumulation was generally greater in species with a comparatively large crown biomass relative to stem size such as C. cunninghamiana and E. camadulensis. Average nutrient accumulation by trees as a percentage of input from effluent was estimated at 19% for N, 9% for P, 1% for Na, 14% for K, 52% for Ca and 32% for Mg.

Results of this study indicate the importance of selecting species on the basis of not only growth but also nutrient accumulation to optimise renovation of wastewater by tree plantations.     

Drought tolerance and rainforest tree growth on a North Queensland rainfall gradient

Three instrumented sites were established in 1985 along a 160-km transect from coastal evergreen rainforest on lowlands near Cairns, through rainforest on the Atherton Tableland, to semideciduous vine forest southwest of Mount Garnet. Mean annual rainfall graded from 2800 mm at coastal site (1), through 1400 mm on Atherton Tableland (2), to 760 mm at inland site (3). Each site was equipped with scaffold towers to provide regular access to upper and middle canopy.

Two shade-intolerant rainforest tree species which occurred at all three sites were used to compare tree growth and water relations; these were Acacia aulacocarpa (brown salwood) which was evergreen, and Melia azederach var. australasica (white cedar) which was leafless during onset of drought. Drought responses from coastal to inland sites were qualitatively different between Acacia and Melia. While Acacia foliage endured persistent low-moisture status, the deciduous habit of Melia provided a means of drought-avoidance.

Mean minimum leaf water-potential for deciduous Melia varied from −1.7 MPa to −2.3 MPa across all sites and seasons. By contrast, evergreen Acacia experienced increasing seasonal drought stress from coast to inland, reducing dry-season water-potentials from −2.1 Mpa to −6.4 Mpa, respectively.

Annual patterns of growth in stem cross-sectional area also varied according to species and site. For Acacia, current annual increment ( ) was 54.1 and 56.9 cm² year⁻¹ for coastal and tableland sites respectively. Acacia at the inland site was only 3.1 cm² year⁻¹.

Present results are relevant to species selection criteria in the tropics, where establishment of rainforest species can be limited by seasonal drought.     

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.     

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.