Tree height in Brazil's ‘arc of deforestation’: Shorter trees in south and southwest Amazonia imply lower biomass

This paper estimates the difference in stand biomass due to shorter and lighter trees in southwest (SW) and southern Amazonia (SA) compared to trees in dense forests in central Amazonia (CA). Forest biomass values used to estimate carbon emissions from deforestation throughout, Brazilian Amazonia will be affected by any differences between CA forests and those in the “arc of deforestation” where clearing activity is concentrated along the southern edge of the Amazon forest. At 12 sites (in the Brazilian states of Amazonas, Acre, Mato Grosso and Pará) 763 trees were felled and measurements were made of total height and of stem diameter. In CA dense forest, trees are taller at any given diameter than those in SW bamboo-dominated open, SW bamboo-free dense forest and SA open forests. Compared to CA, the three forest types in the arc of deforestation occur on more fertile soils, experience a longer dry season and/or are disturbed by climbing bamboos that cause frequent crown damage. Observed relationships between diameter and height were consistent with the argument that allometric scaling exponents vary in forests on different substrates or with different levels of natural disturbance. Using biomass equations based only on diameter, the reductions in stand biomass due to shorter tree height alone were 11.0, 6.2 and 3.6%, respectively, in the three forest types in the arc of deforestation. A prior study had shown these forest types to have less dense wood than CA dense forest. When tree height and wood density effects were considered jointly, total downward corrections to estimates of stand biomass were 39, 22 and 16%, respectively. Downward corrections to biomass in these forests were 76 Mg ha⁻¹ (∼21.5 Mg ha⁻¹ from the height effect alone), 65 Mg ha⁻¹ (18.5 Mg ha⁻¹ from height), and 45 Mg. ha⁻¹ (10.3 Mg ha⁻¹ from height). Hence, biomass stock and carbon emissions are overestimated when allometric relationships from dense forest are applied to SW or SA forest types. Biomass and emissions estimates in Brazil's National Communication under the United Nations Framework Convention on Climate Change require downward corrections for both wood density and tree height.     

Above- and belowground biomass in a Brazilian Cerrado

Cerrado is a biome that occupies about 25% of the Brazilian territory and is characterized by a gradient of grassland to savanna and forest formations and by high species richness. It has been severely affected by degradation and deforestation and has been heavily fragmented over the past 4-5 decades. Despite the recognized overall ecological importance of the Cerrado, there are only few studies focusing on the quantification of biomass in this biome. We conducted such a case study in the South-East of Brazil in a cerrado sensu stricto (cerrado s.s.) with the goal to produce estimates of above- and belowground biomass and to develop allometric equations. A number of 120 trees from 18 species were destructively sampled and partitioned into the components: leaves, branches and bole. Five models with DBH (D), height (H), D²H and wood density (WD) as independent variables were tested for the development of allometric models for individual tree aboveground biomass (leaves + branches + bole). One model based on basal area (BA) as a stand parameter was also tested as an alternative approach for predicting aboveground biomass in the stand level. Belowground biomass was estimated by subsampling on 10 sample plots. Mean aboveground tree biomass (bole, branches and leaves) was estimated to be 62,965.5 kg ha⁻¹(SE = 14.6%) and belowground biomass accounted for 37,501.8 kg ha⁻¹ (SE = 23%). The best-fit equation for the estimation of individual tree aboveground biomass include DBH and wood density as explanatory variables (R² = 0.898; SEE = 0.371) and is applicable for the diameter range of this study (5.0-27.6 cm) and in environments with similar conditions of the cerrado s.s. sampled. In the stand level, the model tested presented a higher goodness of fit than the single tree models (R² = 0.934; SEE = 0.224). Our estimates of aboveground biomass are higher than reported by other studies developed in the same physiognomy, but the estimates of belowground biomass are within the range of values reported in other studies from sites in cerrado s.s. Both biomass estimates, however, exhibit relatively large standard errors. The root-to-shoot ratio of the sample trees is in the magnitude of reported values for savanna ecosystems, but smaller than estimated from other studies in the cerrado s.s.     

Biomass functions and expansion factors in young Norway spruce (Picea abies [L.] Karst) trees

Roots, stems, branches and needles of 160 Norway spruce trees younger than 10 years were sampled in seven forest stands in central Slovakia in order to establish their biomass functions (BFs) and biomass expansion factors (BEFs). We tested three models for each biomass pool based on the stem base diameter, tree height and the two parameters combined. BEF values decreased for all spruce components with increasing height and diameter, which was most evident in very young trees under 1 m in height. In older trees, the values of BEFs did tend to stabilise at the height of 3–4 m. We subsequently used the BEFs to calculate dry biomass of the stands based on average stem base diameter and tree height. Total stand biomass grew with increasing age of the stands from about 1.0 Mg ha⁻¹ at 1.5 years to 44.3 Mg ha⁻¹ at 9.5 years. The proportion of stem and branch biomass was found to increase with age, while that of needles was fairly constant and the proportion of root biomass did decrease as the stands grew older.     

Above- and belowground nutrients storage and biomass accumulation in marginal Nothofagus antarctica forests in Southern Patagonia

The above- and belowground biomass and nutrient content (N, P, K, Ca, S and Mg) of pure deciduous Nothofagus antarctica (Forster f.) Oersted stands grown in a marginal site and aged from 8 to 180 years were measured in Southern Patagonia. The total biomass accumulated ranged from 60.8 to 70.8 Mg ha⁻¹ for regeneration and final growth stand, respectively. The proportions of belowground components were 51.6, 47.2, 43.9 and 46.7% for regeneration, initial growth, final growth and mature stand, respectively. Also, crown classes affected the biomass accumulation where dominant trees had 38.4 Mg ha⁻¹ and suppressed trees 2.6 Mg ha⁻¹ to the stand biomass in mature stand. Nutrient concentrations varied according to tree component, crown class and stand age. Total nutrient concentration graded in the fallowing order: leaves > bark > middle roots > small branches > fine roots > sapwood > coarse roots > heartwood. While N and K concentrations increased with age in leaves and fine roots, concentration of Ca increased with stand age in all components. Dominant trees had higher N, K and Ca concentrations in leaves, and higher P, K and S concentrations in roots, compared with suppressed trees. Although the stands had similar biomass at different ages, there were important differences in nutrient accumulation per hectare from 979.8 kg ha⁻¹ at the initial growth phase to 665.5 kg ha⁻¹ at mature stands. Nutrient storage for mature and final growth stands was in the order Ca > N > K > P > Mg > S, and for regeneration stand was Ca > N > K > Mg > P > S. Belowground biomass represented an important budget of all nutrients. At early ages, N, K, S, Ca and Mg were about 50% in the belowground components. However, P was 60% in belowground biomass and then increased to 70% in mature stands. These data can assist to quantify the impact of different silviculture practices which should aim to leave material (mainly leaves, small branches and bark) on the site to ameliorate nutrient removal and to avoid a decline of long-term yields.     

Ontogeny partly explains the apparent heterogeneity of published biomass equations for Fagus sylvatica in central Europe

A set of robust biomass equations was developed for European beech (Fagus sylvatica), using a large database made of trees from three different European countries. Models were calibrated on the French control dataset, including a broad range of tree size, age and geographical conditions. Their independent validation on Belgian, German unfertilized, German and French fertilized stands gave very promising unbiased results for all of the main tree compartments. The basic fitted allometric equation (biomass = β × (d²h)^γ) allowed us to work with biologically meaningful parameters, where β encompasses both the form of the tree and the wood density, and γ is the allometric exponent that indicates the proportionality between the biomass and volume relative increments. The allometric parameters were found to vary with stand age (decreasing for the crown and increasing for the bole), and introducing these parameters to the equations significantly improved the performance of all aboveground biomass equations. This age effect was related to changes in both stem form and wood density for the trunk and to changes in hydraulic conductance for the crown. We argue that introducing stand age into the predictive parameters is the key for the accuracy of our equations. Management options and stand fertility stand for the low residual variations around this relationship. To confirm this result, we were able to homogenize most of the published biomass equations by accounting for the stand age given in each original paper. We noticed that our results were consistent with and matched the patterns that were observed for Eucalyptus (Eucalyptus). This could mean that species with similar wood properties and crown architecture may exhibit similar biomass equation structures.     

Predicting growth and sequestration of carbon by plantations growing in regions of low-rainfall in southern Australia

In regions of Australia of low–medium rainfall (500–800 mm/year), there is growing community and land-owner support for re-planting trees to achieve multiple environmental objectives, particularly amelioration of soil salinity. Sequestration of carbon by newly established trees is not only another important environmental benefit, but also a potential commercial benefit. To obtain estimates of carbon sequestered by species of commercial potential in such regions, we calibrated the carbon (C) accounting model FullCAM to Eucalyptus cladocalyx and Corymbia maculata plantations. This was achieved by harvesting trees of a range in sizes to determine the allometric relationships that most accurately predict biomass and stem density from measures of stem diameter. Predictions of stem diameter were obtained from a forest growth model (3-PG) previously calibrated for these two species. By applying these predictions of changes in stem diameter as the stand matures in our allometric relationships, we estimated changes in partitioning of biomass (between stem, branches, bark, foliage and roots) and stem wood density as the stand matures under scenarios of 500, 600 and 750 mm mean annual rainfall. We found that for both species, regardless of annual rainfall, throughout the rotation 37–50% of carbon sequestered in the total tree biomass was in the stem, 18–27% in both branches and roots, and the remainder in foliage or bark. However, rate of accumulation of carbon was dependent on annual rainfall, with average annual rate of sequestration of carbon in tree biomass and litter during the first rotation of E. cladocalyx (or C. maculata) increasing from 3.68 (or 4.17) to 4.72 (or 4.86) Mg C ha⁻¹ yr⁻¹ as annual rainfall increased from about 500 to 750 mm. Although it was predicted that decomposition negated any accumulation of debris between successive rotations, carbon was predicted to accumulate in sawlog products, given that assumed rates of product decomposition were slightly less than their rate of accumulation. This resulted in a slight increase (<8 Mg C ha⁻¹) in predicted total sequestration of carbon between successive rotations.     

Wood density in forests of Brazil's ‘arc of deforestation’: Implications for biomass and flux of carbon from land-use change in Amazonia

Wood density is an important variable in estimates of forest biomass and greenhouse-gas emissions from land-use change. The mean wood density used in estimates of forest biomass in the Brazilian Amazon has heretofore been based on samples from outside the “arc of deforestation”, where most of the carbon flux from land-use change takes place. This paper presents new wood density estimates for the southern and southwest Brazilian Amazon (SSWA) portions of the arc of deforestation, using locally collected species weighted by their volume in large local inventories. Mean wood density was computed for the entire bole, including the bark, and taking into account radial and longitudinal variation. A total of 403 trees were sampled at 6 sites. In the southern Brazilian Amazon (SBA), 225 trees (119 species or morpho-species) were sampled at 4 sites. In eastern Acre state 178 trees (128 species or morpho-species) were sampled at breast height in 2 forest types. Mean basic density in the SBA sites was 0.593 ± 0.113 (mean ± 1 S.D.; n = 225; range 0.265–0.825). For the trees sampled in Acre the mean wood density at breast height was 0.540 ± 0.149 (n = 87) in open bamboo-dominated forest and 0.619 ± 0.149 (n = 91) in dense bamboo-free forest. Mean wood density in the SBA sites was significantly higher than in the bamboo dominated forest but not the dense forest at the Acre site. From commercial wood inventories by the RadamBrasil Project in the SSWA portion of the arc of deforestation, the wood volume and wood density of each species or genus were used to estimate average wood density of all wood volume in each vegetation unit. These units were defined by the intersection of mapped forest types and states. The area of each unit was then used to compute a mean wood density of 0.583 g cm⁻³ for all wood volume in the SSWA. This is 13.6% lower than the value applied to this region in previous estimates of mean wood density. When combined with the new estimates for the SSWA, this gave an average wood density of 0.642 g cm⁻³ for all the wood volume in the entire Brazilian Amazon, which is 7% less than a prior estimate of 0.69 g cm⁻³. These results suggest that current estimates of carbon emissions from land-use change in the Brazilian Amazon are too high. The impact on biomass estimates and carbon emissions is substantial because the downward adjustment is greater in forest types undergoing the most deforestation. For 1990, with 13.8 × 10³ km² of deforestation, emissions for the Brazilian Amazon would be reduced by 23.4–24.4 × 10⁶ Mg CO₂-equivalent C/year (for high- and low-trace gas scenarios), or 9.4–9.5% of the gross emission and 10.7% of the net committed emission, both excluding soils.     

Tree biomass estimation in regenerating areas of tropical dry vegetation in northeast Brazil

Allometric equations have been developed for various different vegetation types but have rarely been validated in the field and never for dry tropical forest such as caatinga. In three areas of semi-arid Brazil, with regenerating caatinga vegetation, we measured and weighed twelve hundred individuals of four tree species and used the data to validate equations previously determined in mature caatinga. They and several other equations developed for tropical vegetations overestimate the biomass (B) of trees from the regeneration areas by more than 20%, possibly because these trees have reduced crowns, with lower branch masses. We then determined new allometric equations for them, validating equations for one site against data of the others and pooling the data if they were cross-validated. The best equations were power ones, based on diameter at breast height (D), with little improvement by including height, crown area and/or wood density (Caesalpinia pyramidalis, B = 0.3129D^1.8838; Croton sonderianus, B = 0.4171D^1.5601; Mimosa ophthalmocentra, B = 0.4369D^1.8493; and Mimosa tenuiflora, B = 0.3344D^1.9648 and 0.4138D^1.7718).     

云南省云杉立木生物量模型研建

以云南云杉为研究对象,对云杉地上生物量和地下生物量模型进行研建。建立云杉地上总生物量、树干、树冠、干材、干皮、树枝、树叶独立模型与材积相容模型,采用分级联合控制和度量误差模型方法,建立地上总生物量和所有分量相容的立木生物量模型,建立根茎比模型对云杉地下生物量进行估计。结果表明：建立的云杉地上总生物量、树干、干材生物量二元模型预估精度均达95％以上,干皮生物量模型预估精度达94％以上,树冠、树叶、树枝生物量的预估精度均在92％以上,地下生物量模型预估精度在88％以上;所建立的模型可以用于云杉生物量的估计。     

Carbon sequestration and biodiversity of re-growing miombo woodlands in Mozambique

Land management in tropical woodlands is being used to sequester carbon (C), alleviate poverty and protect biodiversity, among other benefits. Our objective was to determine how slash-and-burn agriculture affected vegetation and soil C stocks and biodiversity on an area of miombo woodland in Mozambique, and how C stocks and biodiversity responded once agriculture was abandoned. We sampled twenty-eight 0.125 ha plots that had previously been cleared for subsistence agriculture and had been left to re-grow for 2 to ∼25 years, and fourteen 0.25 ha plots of protected woodlands, recording stem diameter distributions and species, collecting wood for density determination, and soil from 0 to 0.3 m for determination of %C and bulk density. Clearance for agriculture reduced stem wood C stocks by 19.0 t C ha⁻¹. There were significant relationships between period of re-growth and basal area, stem numbers and stem biomass. During re-growth, wood C stocks accumulated at 0.7 t C ha⁻¹ year⁻¹. There was no significant difference in stem C stocks on woodlands and on abandoned farmland 20–30 years old. Soil C stocks in the top 0.3 m on abandoned land had a narrower range (21–74 t C ha⁻¹) than stocks in woodland soils (18–140 t C ha⁻¹). There was no discernible increase in soil C stocks with period of re-growth, suggesting that the rate of accumulation of organic matter in these soils was very slow. The re-growing plots did not contain the defining miombo species, and total stem numbers were significantly greater than in woodland plots, but species richness and diversity were similar in older abandonments and miombo woodlands. Wood C stocks on abandoned farmland were capable of recovery within 2–3 decades, but soil C stocks did not change on this time-scale. Woodland soils were capable of storing >100 t C ha⁻¹, whereas no soil on a re-growing area exceeded 74 t C ha⁻¹, so there is a potential for C sequestration in soils on abandoned farmland. Management should focus on identifying C-rich soils, conserving remaining woodlands to protect soil C and preserve defining miombo species, and on investigating whether fire control on recovering woodland can stimulate accumulation of soil C and greater tree biomass, and restore defining miombo species.     

西非Sudanian热带林地11个树种地上生物量异速生长预测

Allometric models are necessary for estimating biomass in terrestrial ecosystems. Generalized allometric relationship exists for many tropical trees, but species- and region-specific models are often lacking. We developed species-specific allometric models to predict aboveground biomass for 11 native tree species of the Sudanian savanna-woodlands. Diameters at the base and at breast height, with species means ranging respectively from 11 to 28 cm and 9 to 19 cm, and the height of the trees were used as predictor variables. Sampled trees spanned a wide range of sizes including the largest sizes these species can reach. As a response variable, the biomass of the trees was obtained through destructive sampling of 4 754 trees during wood harvesting. We used a stepwise multiple regression analysis with backward elimination procedure to develop models separately predicting, total biomass of the trees, stem biomass, and biomass of branches and twigs. All species-specific regression models relating biomass with measured tree dimensions were highly significant (p < 0.001). The biomass of branches and twigs was less predictable compared to stem biomass and total biomass, although their models required fewer predictors and predictor interactions. The best-fit equations for total above-ground biomass and stem biomass had R ² > 0.70, except for the Acacia species; for branches including twig biomass, R²-values varied from 0.749 for Anogeissus leiocarpa to 0.183 for Acacia macrostachya. The use of these equations in estimating available biomass will avoid destructive sampling, and aid in planning for sustainable use of these species.     

Carbon accumulation along a stand development sequence of Nothofagus antarctica forests across a gradient in site quality in Southern Patagonia

Above- and below-ground C pools were measured in pure even-aged stands of Nothofagusantarctica (Forster f.) Oersted at different ages (5–220 years), crown and site classes in the Patagonian region. Mean tissue C concentration varied from 46.3% in medium sized roots of dominant trees to 56.1% in rotten wood for trees grown in low quality sites. Total C concentration was in the order of: heartwood > rotten wood > sapwood > bark > small branches > coarse roots > leaves > medium roots > fine roots. Sigmoid functions were fitted for total C accumulation and C root/shoot ratio of individual trees against age. Total C accumulated by mature dominant trees was six times greater than suppressed trees in the same stands, and total C accumulated by mature dominant trees grown on the best site quality was doubled that of those on the lowest site quality. Crown classes and site quality also affected the moment of maximum C accumulation, e.g. dominant trees growing on the worse site quality sequestered 0.73 kg C tree⁻¹ year⁻¹ at 139 years compared to the best site where 1.44 kg C tree⁻¹ year⁻¹ at 116 years was sequestered. C root/shoot ratio decreased over time from a maximum value of 1.3–2.2 at 5 years to a steady-state asymptote of 0.3–0.7 beyond 60 years of age depending on site quality. Thus, root C accumulation was greater during the regeneration phase and for trees growing on the poorest sites. The equations developed for individual trees have been used to estimate stand C accumulation from forest inventory data. Total stand C content ranged from 128.0 to 350.9 Mg C ha⁻¹, where the soil C pool represented 52–73% of total ecosystem C depending on age and site quality. Proposed equations can be used for practical purposes such as estimating the impact of silvicultural practices (e.g. thinning or silvopastoral systems) on forest C storage or evaluating the development of both above- and below-ground C over the forest life cycle for different site qualities for accurate quantification of C pools at regional scale.     

Influence of gaps on some selected tree characteristics of edge trees in Norway spruce plantations

The present study examined branch and stem characteristics of trees growing around gaps in Norway spruce plantations. Trees located at the edge of gaps with a radius of either 5 m or 7 m either unplanted or with supplementary planting were compared to trees in the original closed plantation. The experiment was carried out in two locations in the south of Sweden and the design included four blocks at each location and one replicate of each treatment in each block. The measurements were carried out on standing and felled trees in 2005 at the time of the first thinning. The results indicate a significant effect of gaps and supplementary planting on the diameter of the largest branch, the number of living branches close to breast height, branch basal area, height to the first living branch and taper. The effect of supplementary planting on branch and stem characteristics was greater in large gaps than in small ones. This study indicated that supplementary planting may be useful in affecting stem-form and branch parameters, although other studies have shown that the trees that result from supplementary planting contribute little to total production.     

Factors controlling deadwood availability and branch decay in two Prosopis woodlands in the Central Monte, Argentina

Deadwood is an important resource commonly used by inhabitants in arid lands. However, the low wood productivity and the presence of multi-stemmed trees restrict the use. Prosopis flexuosa woodlands are protected and inhabited by pastoralists who have land rights to use natural resources. As in other forests in the world, dead branches are the most commonly used. The factors causing the death of branches these trees are unknown. As P. flexuosa is a highly heliophilous species, branch mortality may depend on the growth habit and orientation of dry branches under the tree crown. With the participation of inhabitants, we assessed the present availability of deadwood in two Prosopis woodlands of different structure (semi-closed and open woodland), and evaluated the formation of deadwood in terms of shape and cardinal location of dry branches under the crown. We developed and compared regression models to estimate the amount of deadwood for erect, semi-erect and decumbent trees, and for the north and south areas under the crown (n = 120 trees). In addition, to determine the period of growth decline and the factors determining branch mortality, we compared annual radial increment between live and dead branches (n = 30 trees; 10 for each tree shape). The total amount of deadwood in adult Prosopis trees is higher in the semi-closed than in the open woodland (8.6 and 4.4 Tn ha⁻¹, respectively). Only tree size determined the amount of deadwood present in each Prosopis tree, since we found no evidence related to the shape of the tree or the position of dry branches in the canopy. Branch decay was a large process of 18-20 years, and branch death appears to be the result of the action of climatic factors (dry period). The results suggest that the use of deadwood by the desert inhabitants is a tool that can potentially be used; however, the use of this resource taking into account the generation rates of deadwood has not been developed in arid lands. These practices at appropriate sites can contribute to a sustainable management of these woodlands, including the removal of deadwood in a model of local management on a site where potential productivity is relatively low.     

Quantifying branch,crown and bole development in Populus tremuloides Michx. from north-eastern British Columbia

Trembling aspen (Populus tremuloides Michx.) from 14 aspen stands ranging in age from 5 to 142 years were destructively sampled to provide branch, crown and bole growth information. Analysis of crown development processes such as branch angle, branch extensional growth, branch crookedness and annual height growth suggested a significant increase in relative branch growth with height and age which was linked to the temporal decline of height growth. Crown class dependent crown length (%) and crown area relationships were observed indicating crown size followed the sequence: open grown trees > dominants > suppressed trees. A significant shift in crown development from vertical to lateral crown expansion was observed as aspen mature.     

Combining empirical models and the process-based model 3-PG to predict Eucalyptus nitens plantations growth in Spain

Empirical, statistically based models were used to describe the growth and development of Eucalyptus nitens plantations for a range of site productivities and the standard biomass and pulp silvicultural regime currently applied in Northern Spain. The results obtained, along with data gathered from a network of 68 plots, 48 trees felled for biomass estimations and 73 trees sampled for foliar area estimation were used to parameterize the 3-PG model for this species in Northern Spain. Most parameters associated with allometric relationships and partitioning (i.e. bark and branch fraction, basic density, age modifier and mortality) were derived from local data, and the remaining parameters were obtained from published studies on E. nitens or default values previously used for E. globulus. The parameterized model was validated with data from three trials measured from age 3 years until age 8-14 years, and performed better than the empirical model in terms of total stand under bark volume, mean diameter at breast height, basal area and foliar biomass. The process-based model was then used to forecast changes in plantations subjected to a clearwood regime, initializing the model at age 3 years, considering 3 prunings, 2 thinnings and lengthening the rotation to 18 years. This integrated regime was able to provide biomass for bioenergy, pulp or fibreboard wood and also solid wood, with thinning operations assisting the financial viability, and was a potentially good alternative for productive sites.     

Effects of genetic entry and competition on above ground biomass production of Norway spruce grown in southern Finland

The effects of genetic entry and competition on the above ground dry biomass production (i.e. stem wood, needles, branches and harvest index) was studied in 20 Norway spruce (Picea abies (L.) Karst.) clones grown in southern Finland. Furthermore, the measured above ground biomass components were compared against the corresponding estimations based on biomass models developed previously. The clones included both Finnish and Russian clones, as well as provenance-hybrids clones. Differences existed between clones in stem dry mass production, but not in harvest index or in crown dry mass. However, the competition caused by neighboring trees also significantly affected above ground dry biomass, as well as the biomass of crown and stem separately. Differences in competition between the clones could not be found. Unlike the dry mass of branches, the dry mass of needles and stem could be estimated well for individual sample trees with the available biomass models. Moreover, the clone with the largest above ground dry biomass production had nearly doubled production, on average, than the average over all clones. Thus, some of the clones showed especially high potential for biomass recovery in energy wood thinning.     

Does selecting for improved growth affect wood quality of Pinus pinaster in Portugal?

The selection criteria for the first generations in the Portuguese Pinus pinaster improvement program have been the growth rate and form traits. In this work we study the consequences of this selection on wood quality traits. This study assesses genetic and phenotypic correlation between growth, wood density components, lignin content and mechanical traits (radial modulus of elasticity and radial modulus of rupture) of 46 half sib families from a progeny trail located in Leiria, Portugal, originated from seed collected in a clonal seed orchard. A total of 552 seventeen-years-old trees (about half of full rotation age) were sampled at 2 m height. Height measured at 12 years old presented a higher genetic control (h² = 0.34) relatively to DBH, measured at 12 and 17 years old respectively (h² = 0.17 and h² = 0.15). The results of this study also showed that DBH growth is more dependent on latewood components than earlywood components and that higher growth in Mediterranean regions can be due to an increase of the period of latewood formation. Further, we can conclude genetic selection based on growth will not result in a decrease of wood density, will not affect the occurrence of spiral grain, and is possible to obtain an increase in the radial modulus of elasticity. The present study also showed that it is possible to select for increased growth with lower lignin proportion. Results also suggest that selection for growth at 12 years will probably not affect negatively the wood properties at 17 years.     

Normalization of wood density in biomass estimates of Amazon forests

Wood density is an important variable in estimates of biomass and carbon flux in tropical regions. However, the Amazon region lacks large-scale wood-density datasets that employ a sampling methodology adequate for use in estimates of biomass and carbon emissions. Normalization of the available datasets is needed to avoid bias in estimates that combine previous studies of wood density that used wood sampling at diverse positions in the bole or with various methods of density determination. This paper examines the question of whether regressions for radial variation and for variation in wood density along the bole, both developed in dense forest in central Amazonia (CA), are suitable for the open forests in southern Amazonia (SA) that are currently the target of most of Amazonia's deforestation activity. The wood density of the heartwood and density of full disks or slices (bark, sapwood and heartwood) in each tree were measured to assess the radial variation. For variation along the length of the bole, wood densities at breast height and at the top of the bole were used. Moisture content of the bole was measured in SA and compared with values reported by studies from CA in similar dense forest. Comparing regressions that predict full-disk density from heartwood density, the pattern of radial variation differs slightly and significantly between the two forest types (ANCOVA p = 0.006); the slopes have similar values but the intercepts differ. Variation along the bole in the two forest types does not differ significantly (p = 0.144), so the CA model for predicting mean bole density from the density of a slice at breast height gives an unbiased estimate of the mean bole density when applied to SA trees. In SA the mean moisture content of the bole was 0.416 (±0.068 S.D.; n = 223 trees). Moisture content of the bole had a strong inverse relationship with basic wood density (r = −0.77), which explains the lower moisture content in the trees in CA relative to SA. A much weaker inverse relationship was found between moisture content and green wood density (r = −0.292). The relationship between wood basic density and green (‘fresh’) density presented in this study provides an alternative means of obtaining basic wood density directly in the field when oven drying of samples is not possible.     

Increasing wood production through old age in tall trees

How long forest trees can sustain wood production with increasing age remains an open question, primarily because whole-crown structure and growth cannot be readily measured from the ground or on felled trees. We climbed and directly measured crown structures and growth rates of 43 un-suppressed individuals (site trees) of the two tallest species – Eucalyptus regnans and Sequoia sempervirens – representing a wide range of tree sizes and ages. In both species, ground-level measurements of annual growth, including height, ring width, and basal area increment, exhibited the oft-reported trend of decreasing growth (or no change in growth) with age, yet wood production of the entire main trunk and whole crown both increased with size and age up to and including the largest and oldest trees we measured. The balance between structural metrics of whole-crown respiratory demands (cambium area, inner bark volume, sapwood volume, and heartwood deposition area) and photosynthetic capacity (leaf area and green bark area) was statistically independent of size but not age. After accounting for the effect of size, trees with lower potential respiratory demands grew more than trees with higher potential respiratory demands per unit photosynthetic area. The strongest determinant of tree energy balance was the ratio of aboveground cambium area to leaf area. Among the site trees we examined, over 85% of the variation in annual wood production was explained by variation in size, and the proportion of total aboveground wood production in appendages (branches, limbs, and reiterated trunks) increased linearly with size. With increasing age in both species, the proportion of annual wood production converted to heartwood increased in main trunks and appendages. The oldest tree we measured produced more heartwood in its main trunk over 651 years (351 m³) than contained in any tree we measured <1500 years old. The two tallest tree species achieve similar stature despite divergent growth dynamics and ecologies. At one extreme, E. regnans attains great size quickly but dies relatively young because trees are susceptible to fire and fungi. At the other extreme, S. sempervirens attains great size more slowly but has a long lifespan because trees resist fire and prioritize investment in decay-resistant heartwood. Increasing wood production as trees age is a mechanism underlying the maintenance of biomass accumulation during forest development and the carbon-sink capacity of old-growth forests.