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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.

2019

Sammendrag

Short-day (SD) treatment is used by forest nurseries to induce growth cessation in Picea abies seedlings. SD treatment may however increase the risk of reflushing in autumn and earlier bud break the following spring. When the start of the SD treatment is early in order to control seedling height, the duration of the SD treatment should be longer in order to prevent reflushing in autumn. However, due to the amount of manual work involved in the short-day treatment, increasing the number of days is undesirable from a practical point of view. Splitting the SD treatment could be a way to achieve both early height control and at the same time avoid autumn bud break with less workload. We tested how different starting dates and durations of SD treatment influenced on morphological and phenological traits. Regardless of timing and duration of the SD treatment, height growth was reduced compared to the untreated controls. Seedlings given split SD (7+7 days interrupted with two weeks in long days) had less height growth than all other treatments. Root collar diameter growth was significantly less in control seedlings than in seedlings exposed to early (7 or 14 days) or split (7+7 days) SD treatment. There were also differences in the frequency of reflushing and bud break timing among the SD treated seedlings, dependent on duration and starting date. If the SD treatment started early, a continuous 14-day SD treatment was not sufficient to avoid high frequencies of reflushing. However, by splitting the SD treatment into two periods of 7+7 days these negative effects were largely avoided, although spring bud break occurred earlier than in the controls.

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Sammendrag

Tree mortality from insect infestations can significantly reduce carbon storage in forest soils. In subarctic birch forests (Betula pubescens), ecosystem C cycling is largely affected by recurrent outbreaks of defoliating geometrid moths (Epirrita autumnata, Operophtera brumata). Here, we show that soil C stocks in birch forests across Fennoscandia did not change up to 8 years after moth outbreaks. We found that a decrease in woody fine roots was accompanied by a lower soil CO2 efflux rate and a higher soil N availability following moth outbreaks. We suggest that a high N availability and less ectomycorrhiza likely contributed to lowered heterotrophic respiration and soil enzymatic activity. Based on proxies for decomposition (heterotrophic respiration, phenol oxidase potential activity), we conclude that a decrease in decomposition is a prime cause why soil C stocks of mountain birch forest ecosystems have not changed after moth outbreaks. Compared to disturbed temperate and boreal forests, a CO2-related positive feedback of forest disturbance on climate change might therefore be smaller in subarctic regions. Betula pubescens; disturbed subarctic forests; Epirrita autumnata; heterotrophic soil respiration; Operophtera brumata; root biomass; soil carbon sequestration; soil CO2 efflux; soil enzyme activity; structural equation modelling.

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Sammendrag

Four species of the destructive forest pathogen Heterobasidion annosum sensu lato (s.l.) are present in Europe: H. annosum sensu stricto (s.s.), H. abietinum and H. parviporum are native species, while H. irregulare is a non‐native invasive species currently reported only in Italy, yet recommended for regulation throughout Europe. In this study, real‐time PCR detection tests were developed for each of the four species, which can be used simultaneously or individually thanks to probes labelled with species‐specific fluorescent dyes. The different performance criteria of each assay were evaluated, and it was determined that they were theoretically capable of detecting amounts of DNA corresponding to 311, 29 and 29 cell nuclei in H. annosum s.s., H. irregulare and H. parviporum, respectively. The specificity of each assay was assessed with a wide set of strains. Real‐time PCR tests successfully detected Heterobasidion species from 36 fruiting bodies taken from the forest, as well as from artificially inoculated or naturally infected wood samples. The multiplex real‐time PCR assays developed in this study could have practical applications both in forest management and in phytosanitary monitoring.

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Sammendrag

The vesicle trafficking inhibitor Brefeldin A (BFA) changes the localization of plasma membrane localized PINs, proteins that function as polar auxin efflux carriers, by inducing their accumulation within cells. Pretreatment with the synthetic auxin 1-NAA reduces this BFA-induced PIN internalization, suggesting that auxinic compounds inhibit the endocytosis of PIN proteins. However, the most important natural auxin, IAA, did not substantially inhibit PIN internalization unless a supplementary antioxidant, butylated hydroxytoluene (BHT), was also included in the incubation medium. We asked whether the relatively small inhibition caused by IAA alone could be explained by its instability in the incubation solution or whether IAA might interact with BHT to inhibit endocytosis. Analysis of the IAA concentration in the incubation solution and of DR5 reporter activity in the roots showed that IAA is both stable and active in the medium. Therefore, IAA degradation was not able to explain the inability of IAA to inhibit endocytosis. Furthermore, when applied in the absence of auxin, BHT caused a strong increase in the rate of PIN1 internalization and a weaker increase in the rate of PIN2 internalization. These increases were unaffected by the simultaneous application of IAA, further indicating that endocytosis is not inhibited by the natural auxin IAA under physiologically relevant conditions. Endocytosis was inhibited at the same rate with 2-NAA, an inactive auxin analog, as was observed with 1-NAA and more strongly than with natural auxins, supporting the idea that this inhibition is not auxin specific.