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2018

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Sammendrag

© 2018. This is the authors’ accepted and refereed manuscript to the article. Locked until 7.9.2020 due to copyright restrictions. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

Sammendrag

Sclerotinia stem rot (SSR) is the most important disease of oilseed Brassica crops in Norway. Fungicide applications should be aligned with the actual need for control, but the SSR prediction models used lack accuracy. We have studied the importance of precipitation, and the role of petal and leaf infection for SSR incidence by using data from Norwegian field and trap plant trials over several years. In the trials, SSR incidence ranged from 0 to 65%. Given an infection threshold of 25% SSR, regression and Receiver Operating Characteristics (ROC) analysis were used to evaluate different precipitation thresholds. The sum of precipitation two weeks before and during flowering appeared to be a poor predictor for SSR infection in our field and trap plant trials (P = 0.24, P = 0.11, respectively). Leaves from three levels (leaf one, three, five), and petals were collected at three to four different times during flowering from nine field sites over two years and tested for SSR infection with real-time PCR. Percentage total leaf and petal infection explained 57 and 45% of variation in SSR incidence, respectively. Examining the different leaves and petals separately, infection of leaf three sampled at full flowering showed the highest explanation of variation in later SSR incidence (R2 = 65%, P < 0.001). ROC analysis showed that given an infection threshold of 45%, both petal and leaf infection recommended spraying when spraying was actually needed. Combining information on petal and leaf infection during flowering with relevant microclimate factors in the canopy, instead of the sum of precipitation might improve prediction accuracy for SSR.

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We investigated the ability of the fungal entomopathogen Beauveria bassiana strain GHA to endophytically colonize sugarcane (Saccharum officinarum) and its impact on plant growth. We used foliar spray, stem injection, and soil drench inoculation methods. All three inoculation methods resulted in B. bassiana colonizing sugarcane tissues. Extent of fungal colonization differed significantly with inoculation method (χ2 = 20.112, d. f. = 2, p < 0.001), and stem injection showed the highest colonization level followed by foliar spray and root drench. Extent of fungal colonization differed significantly with plant part (χ2 = 33.072, d. f. = 5, p < 0.001); stem injection resulted in B. bassiana colonization of the stem and to some extent leaves; foliar spray resulted in colonization of leaves and to some extent, the stem; and soil drench resulted in colonization of roots and to some extent the stem. Irrespective of inoculation method, B. bassiana colonization was 2.8 times lower at 14–16 d post inoculation (DPI) than at 7–10 DPI (p = 0.020). Spraying leaves and drenching the soil with B. bassiana significantly (p = 0.01) enhanced numbers of sett roots. This study demonstrates for the first time that B. bassiana can endophytically colonize sugarcane plants and enhance the root sett and it provides a starting point for exploring the use of this fungus as an endophyte in management of sugarcane pests.