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Publikasjoner

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.

2023

Sammendrag

Tap av organisk materiale, jordpakking og erosjon truer jordhelsa på kornareal. Problemer med dette vil antagelig øke i et våtere klima og medføre store kostnader for både gårdbrukere og samfunn. Fremover må vi passe på å stabilisere erosjonsutsatt jordoverflate og sikre en god infiltrasjon av nedbør. På kornareal er lav årlig tilførsel av karbon en begrensende faktor for aggregering og stabilisering, men dette kan forbedres ved å beholde halmen på jordet eller bruke en tilpasset fangvekststrategi. En bør trolig skjevfordele tilført organisk materiale mer mot jordas overflate og dermed stimulere mikrobiell aktivitet i jordas toppsjikt. Da må en minimere jordarbeidingsintensiteten. Slik redusert jordarbeiding fører også til utvikling av et kontinuerlig poresystem nedover i profilet som kan øke infiltrasjonen etter kraftige nedbørsepisoder og dermed bidra til å dempe flomtopper. Store mengder plantemateriale ved jordoverflaten gir imidlertid også noen utfordringer. Det trengs økt kunnskap om ugrasbekjempelse, spesielt i et scenario der glyfosat blir forbudt. Minimal jordarbeiding med planterester på jordoverflaten kan også øke angrep av sopp. Integrerte plantevernstrategier bør identifisere arter og sorter av matplanter og fangvekster som kan bidra til å begrense forekomst av patogener i jord og halmrester. Bedre jordhelse på kornareal er en tverrfaglig utfordring og krever en varig endring av dagens dyrkingspraksis.

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Sammendrag

In Norway, cover crops were introduced to prevent loss of nitrogen and phosphorous from fields to waterways. Today, cover crops are also used to restore soil organic matter and improve soil health. Yet, the direction and magnitude of these effects are variable, and little is known about the persistence of the C derived from the cover crops in the soil. In the CAPTURE project, we evaluated the soil C sequestration potential from different cover crops used in the main cereal production areas in Norway. To do so, we used pulse labelling with 13C (CO2) to label four different cover crop species Italian ryegrass, phacelia, oilseed radish and summer vetch through their growing period. Cover crops were grown in a monoculture to enable the labelling. The results of the first year of the experiment show that cover crops produced 10- 14 Mg ha-1 above ground biomass, corresponding to 4-6 Mg C ha-1. At the end of the growing season, 3-5% of cover crop C was found in the soil particulate organic matter (POM) fraction and 2-4% in the soil mineral organic matter fraction (MAOM). In the following years, the fate of C derived from the cover crops in the soil will be determined. Furthermore, the soil C sequestration of the different cover crops will be scaled to barley plots in the same experiment, to which cover crops had been undersown in spring or summer. In these plots, N2O emissions have been measured through the whole year. The greenhouse gas trade-offs of cover crops in Norwegian cereal production will be estimated.

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Sammendrag

Peatlands cover only 3–4% of the Earth’s surface, but they store nearly 30% of global soil carbon stock. This significant carbon store is under threat as peatlands continue to be degraded at alarming rates around the world. It has prompted countries worldwide to establish regulations to conserve and reduce emissions from this carbon rich ecosystem. For example, the EU has implemented new rules that mandate sustainable management of peatlands, critical to reaching the goal of carbon neutrality by 2050. However, a lack of information on the extent and condition of peatlands has hindered the development of national policies and restoration efforts. This paper reviews the current state of knowledge on mapping and monitoring peatlands from field sites to the globe and identifies areas where further research is needed. It presents an overview of the different methodologies used to map peatlands in nine countries, which vary in definition of peat soil and peatland, mapping coverage, and mapping detail. Whereas mapping peatlands across the world with only one approach is hardly possible, the paper highlights the need for more consistent approaches within regions having comparable peatland types and climates to inform their protection and urgent restoration. The review further summarises various approaches used for monitoring peatland conditions and functions. These include monitoring at the plot scale for degree of humification and stoichiometric ratio, and proximal sensing such as gamma radiometrics and electromagnetic induction at the field to landscape scale for mapping peat thickness and identifying hotspots for greenhouse gas (GHG) emissions. Remote sensing techniques with passive and active sensors at regional to national scale can help in monitoring subsidence rate, water table, peat moisture, landslides, and GHG emissions. Although the use of water table depth as a proxy for interannual GHG emissions from peatlands has been well established, there is no single remote sensing method or data product yet that has been verified beyond local or regional scales. Broader land-use change and fire monitoring at a global scale may further assist national GHG inventory reporting. Monitoring of peatland conditions to evaluate the success of individual restoration schemes still requires field work to assess local proxies combined with remote sensing and modeling. Long-term monitoring is necessary to draw valid conclusions on revegetation outcomes and associated GHG emissions in rewetted peatlands, as their dynamics are not fully understood at the site level. Monitoring vegetation development and hydrology of restored peatlands is needed as a proxy to assess the return of water and changes in nutrient cycling and biodiversity.

Sammendrag

NIBIO har overvåket og vurdert risikoaspektene ved tungmetallopptak i matplanter gjennom et kunnskapsutviklingsprosjekt som rapporteres her. NIBIO foreslår at det foretas en systematisk kartlegging av alunskiferjord basert på kjemiske analyser. Dette vil dokumentere omfanget samt redusere risiko for overskridelser ved å øke forutsigbarheten for dyrkere. Videre vil det være et viktig grunnlag for å vurdere hvordan EUs nye grenseverdier kan håndteres i Norge, herunder situasjoner med grønsaksavlinger som overskrider grenseverdiene. Sistnevnte vil være av stor betydning for grønnsaksprodusenter i alunskiferområder.

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Sammendrag

Plants provide not only food and feed, but also herbal medicines and various raw materials for industry. Moreover, plants can be green factories producing high value bioproducts such as biopharmaceuticals and vaccines. Advantages of plant-based production platforms include easy scale-up, cost effectiveness, and high safety as plants are not hosts for human and animal pathogens. Plant cells perform many post-translational modifications that are present in humans and animals and can be essential for biological activity of produced recombinant proteins. Stimulated by progress in plant transformation technologies, substantial efforts have been made in both the public and the private sectors to develop plant-based vaccine production platforms. Recent promising examples include plant-made vaccines against COVID-19 and Ebola. The COVIFENZ® COVID-19 vaccine produced in Nicotiana benthamiana has been approved in Canada, and several plant-made influenza vaccines have undergone clinical trials. In this review, we discuss the status of vaccine production in plants and the state of the art in downstream processing according to good manufacturing practice (GMP). We discuss different production approaches, including stable transgenic plants and transient expression technologies, and review selected applications in the area of human and veterinary vaccines. We also highlight specific challenges associated with viral vaccine production for different target organisms, including lower vertebrates (e.g., farmed fish), and discuss future perspectives for the field.

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Sammendrag

Questions Observations in permanent forest vegetation plots in Norway and elsewhere indicate that complex changes have taken place over the period 1988–2020. These observations are summarised in the “climate-induced understorey change (CIUC)” hypothesis, i.e. that the understorey vegetation of old-growth boreal forests in Norway undergoes significant long-term changes and that these changes are consistent with the ongoing climate change as an important driver. Seven testable predictions were derived from the CIUC hypothesis. Location Norway. Methods Vegetation has been monitored in a total of 458 permanently marked plots, each 1 m2, in nine old-growth forest sites dominated by Picea abies at intervals of 5–8 years over the 32-year study period. For each of the 52 combinations of site and year, we obtained response variables for the abundance of single species, abundance and species density of taxonomic–ecological species groups and two size classes of cryptogams, and site species richness. All of these variables were subjected to linear regression modelling with site and year as predictors. Results Mean annual temperature, growing-season length and the number of days with precipitation were higher in the study period than in the preceding ca. 30-year period, resulting in increasingly favourable conditions for bryophyte growth. Site species richness decreased by 13% over the 32-year study period. On average, group abundance of vascular plants decreased by 24% (decrease in forbs: 38%). Patterns of group abundance change differed among cryptogam groups: although peat-moss abundance increased by 39%, the abundance of mosses, hepatics and lichens decreased by 13%, 49% and 67%, respectively. Group abundance of small cryptogams decreased by 61%, whereas a 13% increase was found for large cryptogams. Of 61 single species tested for abundance change, a significant decrease was found for 43 species, whereas a significant increase was found only for 6 species. Conclusions The major patterns of change in species richness, group species density and group abundance observed over the 32-year study period accord with most predictions from the CIUC hypothesis and are interpreted as direct and indirect responses to climate change, partly mediated through changes in the population dynamics of microtine rodents. The more favourable climate for bryophyte growth explains the observed increase for a few large bryophyte species, whereas the decrease observed for small mosses and hepatics is interpreted as an indirect amensalistic effect, brought about by shading and burial in mats of larger species and accelerated by reduced fine-scale disturbance by microtine rodents. Indirect effects of a thicker moss mat most likely drive the vascular plant decline although long-term effects of tree-stand dynamics and former logging cannot be completely ruled out. Our results suggest that the ongoing climate change has extensive, cascading effects on boreal forest ecosystems. The importance of long time-series of permanent vegetation plots for detecting and understanding the effects of climate change on boreal forests is emphasised.