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.
2010
Authors
Eivind Vangdal Sigrid Flatland Ingvild Kristine MehlAbstract
No abstract has been registered
Abstract
Scenarios of climate changes indicate longer and more frequent spells of mild weather during winter in northern latitudes. De-hardening in perennial grasses could increase the risk of frost kill. In this study, the resistance to de-hardening of different grass species and cultivars was examined, and whether the resistance changes during winter or between years, was tested. In Experiment 1, two cultivars of timothy (Phleum pratense L.) and perennial ryegrass (Lolium perenne L.) of contrasting winter hardiness were grown under ambient winter conditions, transferred from the field in January and April 2006 to the laboratory for 9 d with controlled de-hardening conditions of 3°C, 9°C and 15°C. The timothy cultivars were tested at 3°C, 6°C and 9°C in a similar experiment (Experiment 2) in January 2007. De-hardening, measured as decrease in frost tolerance (LT50), was less in timothy than in perennial ryegrass and increased with increasing temperatures. The northern winter-hardy cultivar Engmo of timothy de-hardened more rapidly than the less-hardy cultivar Grindstad, but had higher initial frost tolerance in both experiments, whereas there was less difference between cultivars of perennial ryegrass in Experiment 1. Cultivar Grindstad of timothy lost all hardiness in early spring at all temperatures, whereas cultivar Engmo maintained some hardiness at 3°C. Cultivar Engmo de-hardened at a lower rate in 2007 than in 2006, in spite of similar frost tolerance at the start of de-hardening treatment in both years. This indicates that the rate of de-hardening was controlled by factors additional to the initial frost tolerance and that autumn weather conditions might be important for the resistance to de-hardening.
Abstract
No abstract has been registered
Authors
Nina OpstadAbstract
No abstract has been registered
Abstract
Plant responses to elevated CO2 are governed by temperature, and at low temperatures the beneficial effects of CO2 may be lost. To document the responses of winter cereals grown under cold conditions at northern latitudes, autumn growth of winter wheat exposed to ambient and elevated levels of temperature (+2.5°C), CO2 (+150 µmol mol-1), and shade (-30%) was studied in open-top chambers under low light and at low temperatures. Throughout the experiment, temperature dominated plant responses, while the effects of CO2 were marginal, except for a positive effect on root biomass. Increased temperature resulted in increased leaf area, total biomass, total root biomass, total stem biomass, and number of tillers, but also a lower content of total sugars and a weaker tolerance to frost. The loss of frost tolerance was related to the larger size of plants grown at elevated temperature. The 30% light reduction under shading did not affect the growth, sugar content, or frost tolerance of winter wheat. At the low temperatures found at high latitudes during autumn, the atmospheric CO2 increase is unlikely to enhance autumn growth of winter wheat to any significant extent, while a temperature increase may have important and major effects on its development and growth.
Abstract
Soil biological properties and CO 2 emission were compared in undisturbed grass and regularly disked rows of a peach plantation. Higher nutrient content and biological activity were found in the undisturbed, grass-covered rows. Significantly higher CO 2 fluxes were measured in this treatment at almost all the measurement times, in all the soil water content ranges, except the one in which the volumetric soil water content was higher than 45%. The obtained results indicated that in addition to the favourable effect of soil tillage on soil aeration, regular soil disturbance reduces soil microbial activity and soil CO 2 emission
Abstract
The Hungarian Detailed Soil Hydrophysical Database, called MARTHA ver2.0 has been developed to collect information on measured soil hydraulic and physical characteristics in Hungary. Recently this is the largest detailed national hydrophysical database, containing controlled information from a total of 15,005 soil horizons. Two commonly used pedotransfer functions were tested to evaluate the accuracy of the predictions on the MARTHA data set, representative for Hungarian soils. In general, the application of both examined pedotransfer functions (Rajkai, 1988; Wösten et al., 1999) was not very successful, because these PTFs are representative for other soil groups. The classification tree method was used to evaluate the effect of soil structure on the goodness of estimations. It was found that using the soil structure data the inaccuracies of soil water retention predictions are more explainable and the structure may serve as a grouping variable for the development of class PTFs.
Authors
Andreas C. Drichoutis Rudolfo M. Jr. Nayga Panagiotis LazaridisAbstract
No abstract has been registered
Abstract
The blue-stain fungus Ceratocystis resinifera colonizes wounds on living Picea spp. and other conifers in Europe and North America. Little is known regarding the pathogenicity of this fungus and consequently, four Norwegian C. resinifera isolates were inoculated on to Norway spruce (Picea abies) using two different techniques. These included single-point inoculations on young trees (two inoculations per tree on 14-year-old trees) and mass-inoculations on older trees (∼200 inoculations per tree on 34-year-old trees). In both experiments, C. resinifera induced minor symptoms that in most cases did not differ significantly from inoculation with sterile agar. The virulent blue-stain fungus C. polonica, which was inoculated for comparative purposes, induced extensive symptoms, causing 83% dead cambium circumference and 82% blue-stained sapwood, and long necrotic lesions in the phloem. The results suggest that C. resinifera is non-pathogenic or only mildly pathogenic to Norway spruce and does not present a threat to these trees.
Authors
Øyvind Johan Korsøen Tim Dempster Jan Erik Fosseidengen Anders Fernø Einar Heegaard Tore S KristiansenAbstract
Farmed Atlantic cod (Gadus morhua) are occasionally exposed to buoyancy changes in sea-cages, through lifting or lowering of cage nets. Physiological processes regulate the level of gas in the closed swim bladders of cod and thus the ability of cod to control their buoyancy. Rapid net lifting may cause positive buoyancy, leading to barotrauma, while net lowering may lead to negative buoyancy and alter cod behaviours. We tested how groups of farmed cod responded immediately after lifting events from 5 different start depths equivalent to 40% pressure reductions, and how long they took to return to pre-lifting pressure levels. In addition, we tested immediate responses and recovery times to cage lowering events equivalent to 100– 300% pressure increases. Trials were conducted with 100 cod of 1.1–1.7 kg in a 63 m3 sea-cage at the lower (5 °C) and upper (16 °C) water temperature limits experienced during culture. Swimming behaviours were measured at fixed intervals before and after cage lifting or lowering, and a feeding test was used to assess appetite. In general, lifting events increased swimming speeds 1.5–4 times and tail beats 2–3 times and fish swam with an average −14° head-down angle, indicating positive buoyancy. The depth before lifting affected the immediate response as the fish became more active after lifting events from shallow compared to deeper depths. Appetite levels decreased for about 2 h after cage lifting, independent of temperature or start depth. The overall recovery time of 8 h after lifting did not depend upon start depth or temperature. Lowering events appeared to cause negative buoyancy. Swimming speeds (1.3–2.3 times) and tail beat frequencies (1.4–2.3 times) increased immediately after cage lowering, and cod swam with an average 30° head-up swimming angle. Neither pressure level nor temperature affected this immediate response. Time to recover to neutral buoyancy for 300% pressure increases took 42–90 h, but only 18–34 h for 100% pressure increases. We conclude that a 40% pressure reduction is an upper limit for lifts of healthy farmed cod. Secondary lifts should not be done until at least 10 h after the first lift. Cage lowering should be done slowly to avoid potentially stressful crowding of negatively buoyant fish on the cage bottom, especially at low temperatures.