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In recent Eucalyptus cold-tolerance trials, E. benthamii has shown good growth rates as well as cold tolerance for USDA Plant Hardiness Zones 8 and 9. This study developed growth and yield models for E. benthamii in the southeastern United States. A network of 182 temporary sample plots of E. benthamii ranging in age from 1.5 to 13.3 years was established, and inventory data were collected. Site quality was determined by fitting a polymorphic site index curve, whereas a function for stand basal area based on age, dominant height, and site occupancy was fitted. Stand-level volume and dry-weight biomass prediction equations were fitted as a function of dominant height and basal area. Based on the growth and yield model results, mean annual increments ranged from 26.4 m3 ha–1 year–1 at rotation age 6 years on the best sites to 13.7 m3 ha–1 year–1 at rotation age 10 years on the poorest sites. This is the first published set of management-oriented models for land managers considering planting E. benthamii in the southeastern United States. [ABSTRACT FROM AUTHOR]

Maximizing initial aboveground woody biomass (AGB) accumulation in order to obtain early payments for carbon stocking is essential for the financial viability of reforestation programs fostered by climate mitigation efforts. Intensive silviculture, i.e., silviculture traditionally used in commercial forestry to maximize productivity and gains, has recently been advocated as a promising approach to enhance AGB accumulation in restoration plantations. However, this approach may hamper natural forest regeneration and ecological succession due to high competition between colonizing plants and planted trees. We investigated the impacts of different silvicultural treatments applied to restoration plantations with 20 native tree species on AGB accumulation and spontaneous regeneration of native woody species in an experiment set up in the Atlantic Forest of Brazil. Intensive silviculture demonstrated a remarkable potential to enhance AGB accumulation in restoration plantations by increasing up to three times the AGB of tree stands (from ~25 to 75 Mg/ha in the 12th year). Intensive fertilization/weed control enhanced AGB accumulation, while higher tree density and the proportion of pioneers did not have a significant effect on AGB over the time. In spite of higher costs (cost increase of 13-19%), the cost-effectiveness for AGB accumulation of intensive silviculture was comparable to that of traditional silviculture applied to restoration (US$50-100/Mg AGB for 3 × 2 m spacing). Contrary to our expectations, we did not find a trade-off between AGB accumulation by planted trees and the spontaneous regeneration of tree species, since intensive silviculture enhanced the regeneration of both planted (total of 12 species) and colonizing woody species (total of 30 species) in the plantation understory. Specifically, a strong association was found between AGB stocks and the abundance and richness of colonizing species, a vast majority of which (90% of species and 95% of individuals) were dispersed by animals. We report a case of positive correlation between AGB stocking and woody species regeneration in the restoration of the Atlantic Forest. Fostering the establishment and maintenance of restoration tree plantations can, in some cases, be a win-win strategy for climate mitigation and biodiversity conservation in human-modified tropical landscapes., (© 2019 by the Ecological Society of America.)

Although highly weathered soils cover considerable areas in tropical regions, little is known about exploration by roots in deep soil layers. Intensively managed Eucalyptus plantations are simple forest ecosystems that can provide an insight into the belowground growth strategy of fast-growing tropical trees. Fast exploration of deep soil layers by eucalypt fine roots may contribute to achieving a gross primary production that is among the highest in the world for forests. Soil exploration by fine roots down to a depth of 10 m was studied throughout the complete cycle in Eucalyptus grandis plantations managed in short rotation. Intersects of fine roots, less than 1 mm in diameter, and medium-sized roots, 1-3 mm in diameter, were counted on trench walls in a chronosequence of 1-, 2-, 3.5-, and 6-year-old plantations on a sandy soil, as well as in an adjacent 6-year-old stand growing in a clayey soil. Two soil profiles were studied down to a depth of 10 m in each stand (down to 6 m at ages 1 and 2 years) and 4 soil profiles down to 1.5-3.0 m deep. The root intersects were counted on 224 m(2) of trench walls in 15 pits. Monitoring the soil water content showed that, after clear-cutting, almost all the available water stored down to a depth of 7 m was taken up by tree roots within 1.1 year of planting. The soil space was explored intensively by fine roots down to a depth of 3 m from 1 year after planting, with an increase in anisotropy in the upper layers throughout the rotation. About 60% of fine root intersects were found at a depth of more than 1 m, irrespective of stand age. The root distribution was isotropic in deep soil layers and kriged maps showed fine root clumping. A considerable volume of soil was explored by fine roots in eucalypt plantations on deep tropical soils, which might prevent water and nutrient losses by deep drainage after canopy closure and contribute to maximizing resource uses.

Intra-annual nutrient (nitrogen, phosphorus, potassium, calcium and magnesium) flux was quantified for Pinus taeda L. at a nutrient-poor, well-drained sandy site in Scotland County, NC, USA where a 2 × 2 factorial of irrigation and nutrition was applied in four replications in a 10-year-old stand with 1200 stems ha(-1). Treatments were applied with the goal of providing optimum nutrition (no nutritional deficiencies) and water availability. Component (foliage, branch, stem and root) nutrient content was estimated monthly for 2 years using nutrient concentration and phenology assessments combined with destructive harvests. Positive flux values indicated nutrient accumulation in the trees while negative values indicated nutrient loss from the trees. Fertilization significantly increased nitrogen, phosphorus, potassium, calcium and magnesium flux 140%, on average, over non-fertilized. Irrigation significantly increased calcium flux 28% while there was no significant irrigation effect on nitrogen, phosphorus, potassium or magnesium. Maximum nutrient fluxes (kg ha(-1) day(-1)) for non-fertilized and fertilized stands were 0.36 and 1.05 for nitrogen, 0.042 and 0.095 for phosphorus, 0.13 and 0.51 for potassium, 0.27 and 0.42 for calcium, and 0.04 and 0.12 for magnesium, respectively. Maximum flux was coincident with ephemeral tissue (foliage and fine root) development and likely would be higher in stands with more foliage than those observed in this study (projected leaf area indices were 1.5 and 3.0 for the non-fertilized and fertilized stands). Minimum nutrient fluxes (kg ha(-1) day(-1)) for non-fertilized and fertilized stands were -0.18 and -0.42 for nitrogen, -0.029 and -0.070 for phosphorus, -0.05 and -0.18 for potassium, -0.04 and -0.05 for calcium, and -0.02 and -0.03 for magnesium, respectively. Minimum fluxes were typically observed in the dormant season and were linked to foliage senescence and branch death. Foliage and branch component nutrient contents were out of phase for nitrogen, phosphorus, potassium and magnesium, indicating nutrient retranslocation and storage in branches prior to foliage development and after foliage senescence. In contrast to current operational fertilizer programs which often target winter application these data suggest the best application times would be during foliage development.

Wood production represents a large but variable fraction of gross primary production (GPP) in highly productive Eucalyptus plantations. Assessing patterns of carbon (C) partitioning (C flux as a fraction of GPP) between above- and belowground components is essential to understand mechanisms driving the C budget of these plantations. Better knowledge of fluxes and partitioning to woody and non-woody tissues in response to site characteristics and resource availability could provide opportunities to increase forest productivity. Our study aimed at investigating how C allocation varied within one apparently homogeneous 90 ha stand of Eucalyptus grandis (W. Hill ex Maiden) in Southeastern Brazil. We assessed annual above-ground net primary production (ANPP: stem, leaf, and branch production) and total belowground C flux (TBCF: the sum of root production and respiration and mycorrhizal production and respiration), GPP (computed as the sum of ANPP, TBCF and estimated aboveground respiration) on 12 plots representing the gradient of productivity found within the stand. The spatial heterogeneity of topography and associated soil attributes across the stand likely explained this fertility gradient. Component fluxes of GPP and C partitioning were found to vary among plots. Stem NPP ranged from 554 g C m(-2) year(-1) on the plot with lowest GPP to 923 g C m(-2) year(-1) on the plot with highest GPP. Total belowground carbon flux ranged from 497 to 1235 g C m(-2) year(-1) and showed no relationship with ANPP or GPP. Carbon partitioning to stem NPP increased from 0.19 to 0.23, showing a positive trend of increase with GPP (R(2) = 0.29, P = 0.07). Variations in stem wood production across the gradient of productivity observed at our experimental site were a result of the variability in C partitioning to different forest system components.

Genetic variation and environmental heterogeneity fundamentally shape the interactions between plants of the same species. According to the resource partitioning hypothesis, competition between neighbors intensifies as their similarity increases. Such competition may change in response to increasing supplies of limiting resources. We tested the resource partitioning hypothesis in stands of genetically identical (clone-origin) and genetically diverse (seed-origin) Eucalyptus trees with different water and nutrient supplies, using individual-based tree growth models. We found that genetic variation greatly reduced competitive interactions between neighboring trees, supporting the resource partitioning hypothesis. The importance of genetic variation for Eucalyptus growth patterns depended strongly on local stand structure and focal tree size. This suggests that spatial and temporal variation in the strength of species interactions leads to reversals in the growth rank of seed-origin and clone-origin trees. This study is one of the first to experimentally test the resource partitioning hypothesis for intergenotypic vs. intragenotypic interactions in trees. We provide evidence that variation at the level of genes, and not just species, is functionally important for driving individual and community-level processes in forested ecosystems.

The release of carbon as CO2 from belowground processes accounts for about 70% of total ecosystem respiration. Insights about factors controlling soil CO2 efflux are constrained by the challenge of apportioning sources of CO2 between autotrophic tree roots (and mycorrhizal fungi) and heterotrophic microorganisms. In some temperate conifer forests, the reduction in soil CO2 efflux after girdling (phloem removal) has been used to separate these sources. Girdling stops the flow of carbohydrates to the belowground portion of the ecosystem, which should slow respiration by roots and mycorrhizae while heterotrophic respiration should remain constant or be enhanced by the decomposition of newly dead roots. Therefore, the reduction in CO2 efflux after girdling should be a conservative estimate of the belowground flux of C from trees. We tested this approach in two tropical Eucalyptus plantations. Tree canopies remained intact for more than 3 months after girdling, showing no reduction in light interception. The reduction in soil CO2 efflux averaged 16-24% for the 3-month period after girdling. The reduction in CO2 efflux was similar for plots with one half of the trees girdled and those with all of the trees girdled. Girdling did not reduce live fine root biomass for at least 5 months after treatment, indicating that large reserves of carbohydrates in the root systems of Eucalyptus trees maintained the roots and root respiration. Our results suggest that the girdling approach is unlikely to provide useful insights into the contribution of tree roots and heterotrophs to soil CO2 efflux in this type of forest ecosystem.