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NIBIOs ansatte publiserer flere hundre vitenskapelige artikler og forskningsrapporter hvert år. Her finner du referanser og lenker til publikasjoner og andre forsknings- og formidlingsaktiviteter. Samlingen oppdateres løpende med både nytt og historisk materiale. For mer informasjon om NIBIOs publikasjoner, besøk NIBIOs bibliotek.

2012

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Biochar soil amendment is advocated to mitigate climate change and improve soil fertility. A concern though, is that during biochar preparation PAHs and dioxins are likely formed. These contaminants can possibly be present in the biochar matrix and even bioavailable to exposed organisms. Here we quantify total and bioavailable PAHs and dioxins in a suite of over 50 biochars produced via slow pyrolysis between 250 and 900 °C, using various methods and biomass from tropical, boreal, and temperate areas. These slow pyrolysis biochars, which can be produced locally on farms with minimum resources, are also compared to biochar produced using the industrial methods of fast pyrolysis and gasification. Total concentrations were measured with a Soxhlet extraction and bioavailable concentrations were measured with polyoxymethylene passive samplers. Total PAH concentrations ranged from 0.07 μg g–1 to 3.27 μg g–1 for the slow pyrolysis biochars and were dependent on biomass source, pyrolysis temperature, and time. With increasing pyrolysis time and temperature, PAH concentrations generally decreased. These total concentrations were below existing environmental quality standards for concentrations of PAHs in soils. Total PAH concentrations in the fast pyrolysis and gasification biochar were 0.3 μg g–1 and 45 μg g–1, respectively, with maximum levels exceeding some quality standards. Concentrations of bioavailable PAHs in slow pyrolysis biochars ranged from 0.17 ng L–1 to 10.0 ng L–1which is lower than concentrations reported for relatively clean urban sediments. The gasification produced biochar sample had the highest bioavailable concentration (162 ± 71 ng L–1). Total dioxin concentrations were low (up to 92 pg g–1) and bioavailable concentrations were below the analytical limit of detection. No clear pattern of how strongly PAHs were bound to different biochars was found based on the biochars’ physicochemical properties.

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In 2002, world leaders made a commitment through the Convention on Biological Diversity (CBD), to achieve a significant reduction in the rate of biodiversity loss by 2010. At the Conference of the Parties of the CBD in Nagoya, Japan in 2010, the target was renewed for 2020. We have developed a Biodiversity Change Index (BCI) to help measure progress towards this target. The BCI is constructed with a two-dimensional resolution, allowing for a direct evaluation of the relative importance of changes in quantity and quality, respectively, to the overall change in biodiversity. Quantity is measured as the area of a specified habitat type and quality as the abundance of indicator species and other habitat quality parameters, such as the proportion of old trees or dead wood in forests. The BCI enables easy comparison of changes in biodiversity between different habitat types and between different regions and nations. We illustrate the use of BCI by calculating the index for the Nordic countries for two common habitat types, farmland and forest, and one habitat type of similar importance in the northern hemisphere; mires. In the period 1990–2005 declines in biodiversity of similar magnitudes are seen for farmland and mires across the Nordic countries, while for forest, trends vary considerably. Our results show that the BCI framework can be a useful tool to communicate the complex issue of biodiversity change in a simple manner. However, in accordance with other studies of biodiversity change we conclude that existing monitoring data are too scarce to consistently calculate BCI for all habitat types in all Nordic countries. In order to reasonably evaluate changes in biodiversity, further efforts towards monitoring programmes to obtain reliable and quality assured data on biodiversity at acceptable spatial and temporal resolutions are needed. Moreover, common methods to apply and harmonise data from different monitoring schemes should be developed.

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Arable weeds are generally distributed in patches, while herbicides are applied uniformly. Herbicides can be saved if only the patches are sprayed, i.e. patch spraying (PS). Bottlenecks for cost-effective PS are weed monitoring technology and valid technology-based decision rules for PS (thresholds). The novel machine vision algorithm Weedcer has been developed as an efficient weed monitoring tool for PS. Weedcer estimates the proportions of young weed leaves and cereal leaves in high resolution red–green–blue images. We conducted field trials to test relative weed cover (RWC) and relative mayweed cover (RMC) estimated by Weedcer as decision rules for PS. RWC is the total weed cover divided by the total plant cover and RMC is the mayweed cover divided by the total plant cover. The main criterion for evaluation and basis of these thresholds was the measured grain yield. Images (about 0.06-m2) were acquired with a GPS guided autonomous field robot in spring, the normal time for spraying seed-propagated broadleaf weeds in both winter – and spring cereals in Norway. Three map-based trials (weed monitoring and spraying in two separate operations) showed that mean RWC per management unit (12.0 × 12.5-m) was generally adequate. In winter wheat heavily infested with scentless mayweed (Tripleurospermum inodorum (L.) Sch.Bip.) and/or scented mayweed (Matricaria recutita L.), the mean RMC per management unit was more adequate. Progress during the project allowed three additional trials conducted in real-time (weed monitoring and spraying in the same operation). These were conducted with the robot in spring cereals, and showed that a weighted moving average of RWC per image was adequate. The sprayed and unsprayed management units in these trials were minimum 3.0 × 3.0-m and 0.5 × 3.0-m, respectively. Results indicated that the Weedcer-based thresholds should be lower in wheat (Triticum aestivum) than in barley (Hordeum vulgare).

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In this study, we address this research question: What effect do an innovation strategy and an innovative working climate have on financial performance in the Norwegian wood industry? Innovation strategy embodies four dimensions: those concerning the degree to which innovation in the form of products, processes, and business systems are embedded in the management values and priorities, and those concerning the degree of expenditure in R&D. An innovative working climate is embodied by team cohesion, supervisory encouragement, resources, autonomy, challenge, and openness to innovation. Previous studies indicate a lack of studies in traditional manufacturing and a lack of studies including both an innovation strategy and a supporting working climate. 241 CEOs answered our survey . The connectional model was tested with structural equation modelling, and all hypotheses received support. This implies that an innovation strategy and an innovative working climate enhance financial performance in traditional manufacturing firms. The results are discussed and implications are made

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Fusarium langsethiae is a recently characterized fungus within the genus Fusarium. It is found as a grain contaminant of small grain cereals such as oats and barley, and to a lesser extent wheat. Fusarium langsethiae is particularly widespread in the Nordic countries and the UK where it poses a serious problem as the main producer of T-2 and HT-2 mycotoxins. The biology of F. langsethiae and its interaction with the plant remains poorly understood, partly hampered by difficulties reproducing a natural level of infection under controlled conditions. The reported study was designed as a series of glasshouse experiments to advance our understanding of F. langsethiae biology by investigating alternative infection routes and its proliferation in oats, Avena sativa. Various methods of seed, soil, and seedling inoculation, boot injection and spray inoculation, were tested. The results clearly show a strong preference of F. langsethiae for the panicle, ruling out alternative infection routes. At relatively low temperatures spray infection, accompanied by prolonged humidity, ensured a thorough establishment of the fungus both at flowering and at early dough stage. Boot injection proved to be a reliable working tool for production of an even and predictable grain infection. Apart from in the panicle, considerable fungal proliferation was only detected in flag leaf nodes, and was a direct consequence of the boot injection method. Fungal presence in the node tissue also correlated with significant stunting of infected shoots. In light of the results the pathogenic and endophytic abilities of F. langsethiae are discussed.