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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.

2007

Sammendrag

Studies of defense mechanisms in Norway spruce Picea abies against the spruce bark beetle Ips typographus show that inducible defenses are triggered by unsuccessful beetle attacks. Moreover, spruce trees can be vaccinated against bark beetle attacks through stem bark inoculation with Ceratocystis polonica, an aggressive fungal associate of Ips typographus. Artificial inoculation with certain other fungi has a similar effect, making treated trees a tougher mach for attacking beetles. A similar enhancement of resistance can be achieved by stem surface treatment with methyl jasmonate. Enhanced resistance is associated with the formation of traumatic resin ducts, and mobilization of phenolic substances in living parenchyma cells. The phenolics appear to mix with the traumatic resin. Similar mechanisms are operating in other conifers. We hypothesize that unsuccessful beetle attacks produce a vaccination effect in the trees, enhancing their resistance to later attack. Adding the effect of induced resistance as a model factor shows an immediate effect on the population dynamics of Ips typographus.

Sammendrag

The area of wood protection is in a period of change. New tools are needed to understand the mode of action, and to further improve the new wood protection systems. A set of useful tools are found among the molecular methods. This paper presents an overview of some of the tools available, and the methods are exemplified by papers within the frame of wood protection issues. However, there is still a great unexplored potential within the field of wood protection by the use of various molecular methods. The majority of the work using molecular methods has been performed on species identification issues and within species variation. This paper lists some new promising molecular methods for wood protection issues and a presentation of a new project. The new project will help to gain some new knowledge about how the fungal decay processes are affected by different wood modification systems.

Sammendrag

The root-rot causing fungus Heterobasidion annosum senso lato is the most devastating pathogen of conifers in Europe. This pathogen enter Norway spruce trees trough the roots and colonizes the tree from within, growing as a saprophyte when established within the dead heartwood and acting as a necrotroph when in contact with living host tissue. Twenty percent of the trees in Norwegian spruce stands tend to be infected and this pathogen that can colonize ten meters up inside the tree trunk, decaying the silvicultural most valuable part of the tree. Despite this high incidence of damage the tree has efficient defences against this pathogen and the attack is eventually fought off if present in the bark or living wood. The tree also has a defense against this internal attack (by Heterobasidion established in the heartwood expanding and invading outward toward the living sapwood) by forming a reaction zone; in this case the host defense is directed inwardly by the still living sapwood toward the central colonized wood. We have in the last years studied the host responses to infection in Norway spruce clones at the transcriptional level and found that the speed of recognition and that spatial defense signalling appears to be the hallmarks of trees with high degree of resistance. We strive to study both partners in this pathosystem from a molecular perspective, and are now focusing on the pathogen and what fungal gene-products are being expressed during the colonization of the heartwood compared to those expressed close to the active host defense (reaction zone) using suppressive subtractive hybridization (SSH) followed by Real-Time RT PCR analysis. In addition the colonization profiles were followed on extracted gDNA using quantitative Real-Time PCR.