Atmospheric impact of bioenergy based on perennial crop (reed canary grass,Phalaris arundinaceae,L.) cultivation on a drained boreal organic soil

Marginal organic soils, abundant in the boreal region, are being increasingly used for bioenergy crop cultivation. Using long‐term field experimental data on greenhouse gas (GHG) balance from a perennial bioenergy crop [reed canary grass (RCG), Phalaris arundinaceae L.] cultivated on a drained organic soil as an example, we show here for the first time that, with a proper cultivation and land‐use practice, environmentally sound bioenergy production is possible on these problematic soil types. We performed a life cycle assessment (LCA) for RCG on this organic soil. We found that, on an average, this system produces 40% less CO₂‐equivalents per MWh of energy in comparison with a conventional energy source such as coal. Climatic conditions regulating the RCG carbon exchange processes have a high impact on the benefits from this bioenergy production system. Under appropriate hydrological conditions, this system can even be carbon‐negative. An LCA sensitivity analysis revealed that net ecosystem CO₂ exchange and crop yield are the major LCA components, while non‐CO₂ GHG emissions and costs associated with crop production are the minor ones. Net bioenergy GHG emissions resulting from restricted net CO₂ uptake and low crop yields, due to climatic and moisture stress during dry years, were comparable with coal emissions. However, net bioenergy emissions during wet years with high net uptake and crop yield were only a third of the coal emissions. As long‐term experimental data on GHG balance of bioenergy production are scarce, scientific data stemming from field experiments are needed in shaping renewable energy source policies.     

Effects of forest management on the carbon dioxide emissions of wood energy in integrated production of timber and energy biomass

The aim of this work was to study the sensitivity of carbon dioxide (CO₂) emissions from wood energy to different forest management regimes when aiming at an integrated production of timber and energy biomass. For this purpose, the production of timber and energy biomass in Norway spruce [Picea abies (L.) Karst] and Scots pine (Pinus sylvestris L.) stands was simulated using an ecosystem model (SIMA) on sites of varying fertility under different management regimes, including various thinning and fertilization treatments over a fixed simulation period of 80 years. The simulations included timber (sawlogs, pulp), energy biomass (small‐sized stem wood) and/or logging residues (top part of stem, branches and needles) from first thinning, and logging residues and stumps from final felling for energy production. In this context, a life cycle analysis/emission calculation tool was used to assess the CO₂ emissions per unit of energy (kg CO₂ MWh^?1) which was produced based on the use of wood energy. The energy balance (GJ ha^?1) of the supply chain was also calculated. The evaluation of CO₂ emissions and energy balance of the supply chain considered the whole forest bioenergy production chain, representing all operations needed to grow and harvest biomass and transport it to a power plant for energy production. Fertilization and high precommercial stand density clearly increased stem wood production (i.e. sawlogs, pulp and small‐sized stem wood), but also the amount of logging residues, stump wood and roots for energy use. Similarly, the lowest CO₂ emissions per unit of energy were obtained, regardless of tree species and site fertility, when applying extremely or very dense precommercial stand density, as well as fertilization three times during the rotation. For Norway spruce such management also provided a high energy balance (GJ ha^?1). On the other hand, the highest energy balance for Scots pine was obtained concurrently with extremely dense precommercial stands without fertilization on the medium‐fertility site, while on the low‐fertility site fertilization three times during the rotation was needed to attain this balance. Thus, clear differences existed between species and sites. In general, the forest bioenergy supply chain seemed to be effective; i.e. the fossil fuel energy consumption varied between 2.2% and 2.8% of the energy produced based on the forest biomass. To conclude, the primary energy use and CO₂ emissions related to the forest operations, including the production and application of fertilizer, were small in relation to the increased potential of energy biomass.     

Life cycle assessment tool for estimating net CO2 exchange of forest production

The study describes an integrated impact assessment tool for the net carbon dioxide (CO₂) exchange in forest production. The components of the net carbon exchange include the uptake of carbon into biomass, the decomposition of litter and humus, emissions from forest management operations and carbon released from the combustion of biomass and degradation of wood‐based products. The tool enables the allocation of the total carbon emissions to the timber and energy biomass and to the energy produced on the basis of biomass. In example computations, ecosystem model simulations were utilized as an input to the tool. We present results for traditional timber production (pulpwood and saw logs) and integrated timber and bioenergy production (logging residues, stumps and roots) for Norway spruce, in boreal conditions in Finland, with two climate scenarios over one rotation period. The results showed that the magnitude of management related emissions on net carbon exchange was smaller when compared with the total ecosystem fluxes; decomposition being the largest emission contributor. In addition, the effects of management and climate were higher on the decomposition of new humus compared with old humus. The results also showed that probable increased biomass growth, obtained under the changing climate (CC), could not compensate for decomposition and biomass combustion related carbon loss in southern Finland. In our examples, the emissions allocated for the energy from biomass in southern Finland were 172 and 188 kg CO₂ MW h^?1 in the current climate and in a CC, respectively, and 199 and 157 kg CO₂ MW h^?1 in northern Finland. This study concludes that the tool is suitable for estimating the net carbon exchange of forest production. The tool also enables the allocation of direct and indirect carbon emissions, related to forest production over its life cycle, in different environmental conditions and for alternative time periods and land uses. Simulations of forest management regimes together with the CC give new insights into ecologically sustainable forest bioenergy and timber production, as well as climate change mitigation options in boreal forests.     

Wood ants are wood ants: deforestation causes population declines in the polydomous wood ant Formica aquilonia

Abstract.  1. One of the main themes in ecology is adaptation for survival in different habitats and the potential of the environment to regulate populations.
2. The effects of clear-cutting on nest-abandonment rate and local population sizes in the polydomous wood ant Formica aquilonia was studied, using uncut forest stands as controls.
3. The nest-abandonment rate was clearly higher in clear-cuts than in forest interiors. In clear-cuts, 39% of pre-deforestation nests and 73% of new bud-nests were abandoned 4–5 years after deforestation, whereas in forest interiors fewer than 2% of nests were abandoned at the same time period. Local population size decreased 30% in clear-cuts, but fewer than 2% in forest interiors.
4. The results demonstrate that despite modern logging practices in which mechanical harming of nest mounds is reduced, nest mounds are abandoned at high rate, and despite frequent establishment of new bud-nests, populations start to decline.
5. The likely reason for the high nest-abandonment rate in clear-cuts is a combination of changed abiotic conditions, resource limitation, and disturbed reproduction.
6. Species that are sensitive to changes in the size of habitat patch, such as F. aquilonia , likely are harmed by logging, even employing biodiversity oriented management practices. Hence there is a need for conservation actions that are based on the size of protection areas.     

Spatial seed and pollen games: dispersal,sex allocation,and the evolution of dioecy

The evolutionary forces shaping within‐ and across‐species variation in the investment in male and female sex function are still incompletely understood. Despite earlier suggestions that in plants the evolution or cosexuality vs. dioecy, as well as sex allocation among cosexuals, is affected by seed and pollen dispersal, no formal model has explicitly used dispersal distances to address this problem. Here, we present a game‐theory model as well as a simulation study that fills in this gap. Our model predicts that dioecy should evolve if seeds and pollen disperse widely and that sex allocation among cosexuals should be biased towards whichever sex function produces more widely dispersing units. Dispersal limitations stabilize cosexuality by reinforcing competition between spatially clumped dispersal units from the same source, leading to saturating fitness returns that render sexual specialization unprofitable. However, limited pollen dispersal can also increase the risk of selfing, thus potentially selecting for dioecy as an outbreeding mechanism. Finally, we refute a recent claim that cosexuals should always invest equally in both sex functions.     

The mismeasurement of sexual selection

Sexual selection can explain major micro‐ and macro‐evolutionary patterns. Much of current theory predicts that the strength of sexual selection (i) is driven by the relative abundance of males and females prepared to mate (i.e. the operational sex ratio, OSR) and (ii) can be generally estimated by calculating intra‐sexual variation in mating success (e.g. the opportunity for sexual selection, I_s). Here, we demonstrate the problematic nature of these predictions. The OSR and I_s only accurately predict sexual selection under a limited set of circumstances, and more specifically, only when mate monopolization is extremely strong. If mate monopolization is not strong, using OSR or I_s as proxies or measures of sexual selection is expected to produce spurious results that lead to the false conclusion that sexual selection is strong when it is actually weak. These findings call into question the validity of empirical conclusions based on these measures of sexual selection.