The paper presents an overview of the results of long-term fertilization and irrigation experiments in stands of Scots pine (Pinus sylvestris L.) and Norway spruce (Picea abies (L.) Karst.). Large increases in stemwood production during the first 12 years of the experiments were achieved by fertilization especially when a balanced mixture of macro- and micronutrients was applied. The effect of irrigation alone was small, but it greatly enhanced the response of the ground vegetation to the application of a balanced fertilizer. Fertilization did not greatly affect the leaf/stemwood biomass ratio, but reduced the ratio of fine roots to total biomass. Drought reduced the coarse-root biomass/fine-root biomass ratio.
Summary1. Recent research has addressed how transgenic residues from arable crops may influence adjacent waterways, aquatic consumers and important ecosystem processes such as litter breakdown rates. With future applications of transgenic plants in forestry, such concerns may apply to forest stream ecosystems. Before any large-scale release of genetically modified (GM) trees, it is therefore imperative to evaluate the effects of genetic modifications in trees on such ecosystems. 2. We conducted decomposition experiments under natural stream conditions using leaf litter from greenhouse grown GM trees (Populus tremula · Populus tremuloides) that express Bacillus thuringiensis (Bt) toxins (cry3Aa; targeting coleopteran leaf-feeding beetles) to examine the hypothesis that GM trees would affect litter decomposition rates and ⁄ or the aquatic arthropod community that colonizes and feeds on leaf litter in streams. 3. We show that two independent transformations of isogenic Populus trees to express Bt toxins caused similar changes to the composition of aquatic insects colonizing the leaf litter, ultimately manifested in a 25% and 33% increases in average insect abundance. 4. Measurements of 24 phenolic compounds as well as nitrogen (N) and carbon (C) in the litter did not significantly differ among modified and wild-type trees and were thus not sufficient to explain these differences in the insect assemblage. 5. Decomposition rates were comparable among litter treatments suggesting that the normal suite of leaf traits influencing decomposition was similar among litter treatments and that the shredding functions of the community were maintained despite the changes in insect community composition. 6. Synthesis and applications. We report that leaf litter from GM trees affected the composition of aquatic insect communities that colonized litter under natural stream conditions. This suggests that forest management using GM trees may affect adjacent waterways in unanticipated ways, which should be considered in future commercial applications of GM trees. We also argue that studies at different scales (e.g. species, communities and ecosystems) will be needed for a full understanding of the environmental effects of Bt plants.
Wood from biomass plantations with fast growing tree species such as poplars can be used as an alternative feedstock for production of biofuels. To facilitate utilization of lignocellulose for saccharification, transgenic poplars with modified or reduced lignin contents may be useful. However, the potential impact of poplars modified in the lignification pathway on ectomycorrhizal (EM) fungi, which play important roles for plant nutrition, is not known. The goal of this study was to investigate EM colonization and community composition in relation to biomass and nutrient status in wildtype (WT, Populus tremula 6Populus alba) and transgenic poplar lines with suppressed activities of cinnamyl alcohol dehydrogenase, caffeate/ 5-hydroxyferulate O-methyltransferase, and cinnamoyl-CoA reductase in a biomass plantation. In different one-year-old poplar lines EM colonization varied from 58% to 86%, but the EM community composition of WT and transgenic poplars were indistinguishable. After two years, the colonization rate of all lines was increased to about 100%, but separation of EM communities between distinct transgenic poplar genotypes was observed. The differentiation of the EM assemblages was similar to that found between different genotypes of commercial clones of Populus 6euramericana. The transgenic poplars exhibited significant growth and nutrient element differences in wood, with generally higher nutrient accumulation in stems of genotypes with lower than in those with higher biomass. A general linear mixed model simulated biomass of oneyear-old poplar stems with high accuracy (adjusted R 2 = 97%) by two factors: EM colonization and inverse wood N concentration. These results imply a link between N allocation and EM colonization, which may be crucial for wood production in the establishment phase of poplar biomass plantations. Our data further support that multiple poplar genotypes regardless whether generated by transgenic approaches or conventional breeding increase the variation in EM community composition in biomass plantations.
Bioassays with a non-target slug (Deroceras spp.) and chemical analyses were conducted using leaf tissue from already existing genetically modified insect-resistant aspen trees to examine whether genetic modifications to produce Bacillus thuringiensis (Bt) toxins could affect plant phytochemistry, which in turn might influence plantherbivore interactions. Three major patterns emerged. First, two independent modifications for Bt resistance affected the phytochemical profiles of leaves such that both were different from the isogenic wild-type (Wt) control leaves, but also different from each other. Among the contributors to these differences are substances with a presumed involvement in resistance, such as salicortin and soluble condensed tannins. Second, bioassays with one Bt line suggest that the modification somehow affected innate resistance (''Innate'' is used here in opposition to the ''acquired'' Bt resistance) in ways such that slugs preferred Bt over Wt leaves. Third, the preference test suggests that the innate resistance in Bt relative to Wt plants may not be uniformly expressed throughout the whole plant and that leaf ontogeny interacts with the modification to affect resistance. This was manifested through an ontogenetic determined increase in leaf consumption that was more than four times higher in Bt compared to Wt leaves. Our result are of principal importance, as these indicate that genetic modifications can affect innate resistance and thus non-target herbivores in ways that may have commercial and/or environmental consequences. The finding of a modification-ontogeny interaction effect on innate resistance may be especially important in assessments of GM plants with a long lifespan such as trees.
Current policy is driving renewed impetus to restore forests to return ecological function, protect species, sequester carbon and secure livelihoods. Here we assess the contribution of tree planting to ecosystem restoration in tropical and sub-tropical Asia; we synthesize evidence on mortality and growth of planted trees at 176 sites and assess structural and biodiversity recovery of co-located actively restored and naturally regenerating forest plots. Mean mortality of planted trees was 18% 1 year after planting, increasing to 44% after 5 years. Mortality varied strongly by site and was typically ca 20% higher in open areas than degraded forest, with height at planting positively affecting survival. Size-standardized growth rates were negatively related to species-level wood density in degraded forest and plantations enrichment settings. Based on community-level data from 11 landscapes, active restoration resulted in faster accumulation of tree basal area and structural properties were closer to old-growth reference sites, relative to natural regeneration, but tree species richness did not differ. High variability in outcomes across sites indicates that planting for restoration is potentially rewarding but risky and context-dependent. Restoration projects must prepare for and manage commonly occurring challenges and align with efforts to protect and reconnect remaining forest areas. The abstract of this article is available in Bahasa Indonesia in the electronic supplementary material. This article is part of the theme issue ‘Understanding forest landscape restoration: reinforcing scientific foundations for the UN Decade on Ecosystem Restoration’.
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