Publications
NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.
2003
Abstract
Spatio-temporal analyses of non-epidemic bark beetle populations may provide insight in dynamics predisposing for outbreaks. The present article presents a spatio-temporal analysis of the population dynamics of Ips typographus based on pheromone trap data from southeast and mid-Norway in the post-epidemic period 19792002. The analyses include regression analyses, hierarchical cluster analysis, and analysis of spatial synchrony of beetle time series and climatic data by means of nonparametric spatial covariance functions. The mean abundance of beetles declined linearly with latitude. In addition, the time series means were higher in areas with high forest productivity and rocky soils predisposed to drought. The time series patterns differed significantly between northern and southern study areas. The regional synchrony of the time series was fairly high (0.38), indicating that some large-scale climatic factor may influence the dynamics. Windfelling was the external variable showing the most parallel pattern of correlation to the beetle dynamics. We thus posit that large windfall events may be a major instigator and synchronizer of beetle outbreaks in areas subjected to regionalized weather systems.
Authors
Guro BrodalAbstract
No abstract has been registered
Abstract
We fogged trees in two pine dominated forests in Norway with a synthetic pyrethroid in order to compare the canopy-dwelling fauna of arthropods between costal (Kvam) and boreal (Sigdal) sites and between old (250-330 years) and mature (60-120 years) trees at Sigdal. Almost 30,000 specimens were assigned to 510 species; only 93 species were present at both sites. Species diversity, as established by rarefaction, was similar in old and mature trees. However, the number of species new to Norway (including nine species new to science) was significantly higher in the old trees. We suggest that the scarcity of old trees, habitat heterogeneity and structural differences between old and mature trees may explain these patterns. Productivity and topographic position at the site of growth explained the between-tree variation in species occurrence for the more abundant species, which were mainly Collembola and Oribatida. Species diversity was similar at the boreal and coastal sites, but there were clear differences in species composition
Abstract
No abstract has been registered
Authors
Stephen Woodward Jan Stenlid Marco Michelozzi Halvor Solheim B. Karlsson Panaghiotis TsopelasAbstract
No abstract has been registered
Authors
Halvor SolheimAbstract
No abstract has been registered
Abstract
No abstract has been registered
Authors
Halvor SolheimAbstract
No abstract has been registered
Abstract
Resultat frå forsøk med ulike dekkesystem for søtkirsebær sin effekt på mikroklima og fruktkvalitet er skildra i ein vitskapleg artikkel på engelsk. Resultata er delvis publisert på norsk i følgjande artikkel: Børve, J., A. Stensvand & M. Meland, 1997. Verknad av plastdekking på rotning hjå søtkirsebær. Informasjonsmøte i plantevern 1997 Grønn forskning 2/97. 252-255.
Abstract
A multiplex real-time PCR assay was developed to monitor the dynamics of the Picea abies-Heterobasidion annosum pathosystem. Tissue cultures and 32-year-old trees with low or high resistance to this pathogen were used as the host material. Probes and primers were based on a laccase gene for the pathogen and a polyubiquitin gene for the host.The real-time PCR procedure was compared to an ergosterol-based quantification method in a tissue culture experiment, and there was a strong correlation product moment correlation coefficient, 0.908) between the data sets. The multiplex real-time PCR procedure had higher resolution and sensitivity during the early stages of colonization and also could be used to monitor the host.In the tissue culture experiment, host DNA was degraded more rapidly in the clone with low resistance than in the clone with high resistance. In the field experiment, the lesions elicited were not strictly proportional to the area colonized by the pathogen.Fungal colonization was more restricted and localized in the lesion in the clone with high resistance, hereas in the clone with low resistance, the fungus could be detected until the visible end of the lesion. Thus, the real-time PCR assay gives better resolution than does the traditionally used lesion length measurement when screening host clones for resistance.