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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.

2021

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Sweet cherry (Prunus avium L.) is a temperate fruit species whose production might be highly impacted by climate change in the near future. Diversity of plant material could be an option to mitigate these climate risks by enabling producers to have new cultivars well adapted to new environmental conditions. In this study, subsets of sweet cherry collections of 19 European countries were genotyped using 14 SSR. The objectives of this study were (i) to assess genetic diversity parameters, (ii) to estimate the levels of population structure, and (iii) to identify germplasm redundancies. A total of 314 accessions, including landraces, early selections, and modern cultivars, were monitored, and 220 unique SSR genotypes were identified. All 14 loci were confirmed to be polymorphic, and a total of 137 alleles were detected with a mean of 9.8 alleles per locus. The average number of alleles (N = 9.8), PIC value (0.658), observed heterozygosity (Ho = 0.71), and expected heterozygosity (He = 0.70) were higher in this study compared to values reported so far. Four ancestral populations were detected using STRUCTURE software and confirmed by Principal Coordinate Analysis (PCoA), and two of them (K1 and K4) could be attributed to the geographical origin of the accessions. A N-J tree grouped the 220 sweet cherry accessions within three main clusters and six subgroups. Accessions belonging to the four STRUCTURE populations roughly clustered together. Clustering confirmed known genealogical data for several accessions. The large genetic diversity of the collection was demonstrated, in particular within the landrace pool, justifying the efforts made over decades for their conservation. New sources of diversity will allow producers to face challenges, such as climate change and the need to develop more sustainable production systems.

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The use of microalgal starch has been studied in biorefinery frameworks to produce bioethanol or bioplastics, however, these products are currently not economically viable. Using starch-rich biomass as an ingredient in food applications is a novel way to create more value while expanding the product portfolio of the microalgal industry. Optimization of starch production in the food-approved species Chlorella vulgaris was the main objective of this study. High-throughput screening of biomass composition in response to multiple stressors was performed with FTIR spectroscopy. Nitrogen starvation was identified as an important factor for starch accumulation. Moreover, further studies were performed to assess the role of light distribution, investigating the role of photon supply rates in flat panel photobioreactors. Starch-rich biomass with up to 30% starch was achieved in cultures with low inoculation density (0.1 g L−1) and high irradiation (1800 µmol m−2 s−1). A final large-scale experiment was performed in 25 L tubular reactors, achieving a maximum of 44% starch in the biomass after 12 h in nitrogen starved conditions.

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ABSTRACT The use of microalgal starch has been studied in biorefinery frameworks to produce bioethanol or bioplastics, however, these products are currently not economically viable. Using starch−rich biomass as an ingredient in food applications is a novel way to create more value while expanding the product portfolio of the microalgal industry. Optimization of starch production in the food−approved species Chlorella vulgaris was the main objective of this study. High−throughput screening of biomass composition in response to multiple stressors was performed with FTIR spectroscopy and nitrogen starvation was identified as an important factor for starch accumulation. Further studies were subsequently performed to assess the role of light distribution, investigating photon supply rates in flat panel photobioreactors. Biomass specific photon supply rate proved to have a strong effect on the accumulation of storage compounds and starch−rich biomass with up to 30% starch was achieved in cultures with low inoculation density (0.1 g L−1) and high irradiation (1800 μmol m−2 s−1). A final large scale experiment was performed in 25 L tubular reactors, achieving a maximum of 44% starch in the biomass after 12 hours in nitrogen starved conditions. Keywords: Chlorella vulgaris, starch, FTIR, photon supply rate, microalgae

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This study attempted to enhance sulfidogenic activity via sulfate-reducing bacteria (SRB) enrichment and minimize organic carbon loss by methanogen inhibition in the sulfidogenic stage of a two-stage anaerobic digestion system (TSADS). To enrich SRB in the sulfidogenic stage, batch tests were performed with various granular sludge pretreatments. Starvation was the most effective pretreatment, increasing SO42− removal and minimizing chemical oxygen demand (COD) loss by inhibiting methanogen activity. Microbial community analysis showed that Desulfovibrio, Desulfotomaculum, and Syntrophobacter were the dominant SRB in the sulfidogenic stage (5.0%, 3.1%, and 2.4%, respectively). This enabled SO42− reduction (86%) and volatile fatty acid production (55% of fed COD) at a hydraulic retention time (HRT) of 4 h. Conversely, biogas with a reduced H2S content (110 ppmv) was produced in the methanogenic stage (HRT = 6 h). A granular sludge comparison revealed differences in their ecology, structure, and extracellular polymeric substance characteristics. Economic feasibility analysis demonstrated that TSADS can lead to a cost reduction of $80–90/1,000 m3 CH4 compared to single-stage anaerobic digestion.

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Eradication of alien invasive species in the soil with steam as an alternative to chemical fumigation may allow contaminated soil to be reused. We have investigated steam disinfestation of soil to combat invasive plant species in three experiments including different temperatures and exposure durations using a prototype stationary soil-steaming device. The experiments included effects on seed germination of bigleaf lupine (Lupinus polyphyllus Lindl.), ornamental jewelweed (Impatiens glandulifera Royle), and wild oat (Avena fatua L.; one population from Poland and one from Norway), as well as effects on sprouting rhizome fragments of Canada goldenrod (Solidago canadensis L.) and Bohemian knotweed (Reynoutria x bohemica Chrtek & Chrtková). In Experiment 1, we tested four different soil temperatures of 64, 75, 79, and 98 C with an exposure duration of 90 s. In Experiments 2 and 3, we tested exposure durations of 30, 90, and 180 s and 90, 180, and 540 s, respectively, at 98 C. Seed pretreatment of 14 d cooling for L. polyphyllus and I. glandulifera, no seed pretreatment and 12-h moistening for A. fatua populations, and 5- and 10-cm cutting size for R. x bohemica were applied. Our results showed germination/sprouting was inhibited at 75 C for I. glandulifera (for 90 s) and 98 C for the other species; however, longer exposure duration was needed for L. polyphyllus. While 30 s at 98 C was enough to kill A. fatua seeds and S. canadensis and R. x bohemica rhizome fragments, 180-s exposure duration was needed to kill L. polyphyllus seeds. The results showed promising control levels of invasive plant propagules in contaminated soil by steaming, supporting the steam treatment method as a potential way of disinfecting soil to prevent dispersal of invasive species.