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.
2005
Abstract
In field experiments, clones of Norway spruce [Picea abies (L.) Karst.] showed different degrees of resistance against pathogenic fungi inoculated into the bark that correlate with differences in polyphenolic parenchyma (PP) cells of the bark. Cells of spruce callus cultures, particularly towards the callus surface, resemble PP cells and this study looks at changes in callus cells during infection and the relative resistance of cultures from clones of low (weak) or high (strong) resistance to fungal infection. Callus cultures, initiated from trees with different resistance, were co-inoculated with Ceratocystis polonica (Siem.) C. Moreau and Heterobasidion annosum (Fr.) Bref. Callus cells from strong clones resemble PP cells of bark tissue from strong clones, having more polyphenolic bodies, while callus cells from weak clones are more similar to PP cells from those clones, which have less extensive phenolic bodies. Callus cultures from trees with weak resistance were more quickly overgrown by both species of pathogenic fungi than cultures from trees with strong resistance. Callus cells of infected cultures showed changes similar to activated PP cells of bark, including enhanced accumulation of polyphenolics. Phenolic bodies were more numerous and more extensive (larger and denser) in callus cells of strong versus weak clones under all conditions. Thus, callus cells may perform similar functions in defense as PP cells in the bark. Callus from trees of varying resistance seem to reflect the relative resistance of the trees from which they are derived, and this study indicates that some mechanisms of resistance can be studied using callus from trees of different resistance.
Authors
Bent Christen Braskerud K.S. Tonderski B. Wedding Rune Bakke A.-G.B. Blankenberg B. Ulen J. KoskiahoAbstract
No abstract has been registered
Authors
Per Gundersen Bjørn Berg W. S. Currie N. B. Dise B. A. Emmett V. Gauci M. Holmberg O. Janne Kjønaas J. Mol-Dijkstra C. van der Salm I. K. Schmidt A. Tietema W. W. Wessel Live Semb Vestgarden C. Akselsson W. De Vries M. Forsius H. Kros Egbert Matzner Filip Moldan K. J. Nadelhoffer L.-O. Nilsson G. J. Reinds U. Rosengren Arne O. Stuanes Richard WrightAbstract
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Authors
Jolanda Roux Halvor Solheim Michael J. WingfieldAbstract
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Authors
Stig Lande Morten Eikenes Mats Westin Marc H. SchneiderAbstract
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Abstract
Considerable knowledge exists about the effect of aluminium (Al) on root vitality, but whether elevated levels of Al affect soil microorganisms is largely unknown. We thus compared soils from Al-treated and control plots of a field experiment with respect to microbial and chemical parameters, as well as root growth and vitality. Soil from a field experiment established in a 50 year old Norway spruce (Picea abies L.) stand where low concentrations of aluminum (0.5 mM AlCl3) had been added weekly or bi-weekly during the growth season for seven years was compared to a control treatment with respect to microbial and chemical parameters, as well as root growth and vitality. Analysis of soil solutions collected using zero tension lysimeters and porous suction cups showed that Al treatment lead to increased concentrations of Al, Ca and Mg and lower pH and [Ca+Mg]/[Al] molar ratio. Corresponding soil analyses showed that soil pH remained unaffected (pH 3.8), that Al increased, while extractable Ca and Mg decreased due to the Al treatment. Root ingrowth into cores placed in the upper 20 cm of the soil during 28 months was not affected by Al additions, neither was the mortality of these roots. The biomass of some taxonomical groups of soil microorganisms in the humus layer, analyzed using specific membrane components (phospholipid fatty acids; PLFAs), was clearly affected by the imposed Al treatment, but less so in the underlying mineral soil. Microbial community structure in the humus layer was also clearly modified by the Al treatment, whereas differences in the mineral horizon were less clear. Shifts in PLFA trans/cis ratios indicative of short term physiological stress were not observed. Yet, aluminium stress was indicated both by changes in community structure and in ratios of single PLFAs for treated/untreated plots. Thus, soil microorganisms were more sensitive indicators of subtle chemical changes in soil than chemical composition and vitality of roots.
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