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.
2022
Forfattere
Julie Ingram Jane Mills Jasmine E. Black Charlotte-Anne Chivers José A. Aznar-Sánchez Annemie Elsen Magdalena Frac Belén López-Felices Paula Mayer-Gruner Kamilla Skaalsveen Jannes Stolte Mia TitsSammendrag
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Sammendrag
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Forfattere
Darius Kviklys Jonas Viškelis Mindaugas Liaudanskas Valdimaras Janulis Kristina Laužikė Giedrė Samuolienė Nobertas Uselis Juozas LanauskasSammendrag
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Forfattere
Aritz Royo-Esnal Andrea Onofri Donato Loddo Jevgenija Necajeva Peter K. Jensen Garifalia Economou Alireza Taab Agnieszka Synowiec Isabel M. Calha Lars Andersson Ahmet Uludag Ilhan Uremis Alistair J. Murdoch Kirsten TørresenSammendrag
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Forfattere
Aritz Royo-Esnal Andrea Onofri Alireza Taab Donato Loddo Jevgenija Necajeva Ahmet Uludag Agnieszka Synowiec Isabel M. Calha Lars Andersson Peter K. Jensen Ilhan Uremis Garifalia Economou Alistair J. Murdoch Kirsten TørresenSammendrag
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Sammendrag
Reusing soil can reduce environmental impacts associated with obtaining natural fresh soil during road construction and analogous activities. However, the movement and reuse of soils can spread numerous plant diseases and pests, including propagules of weeds and invasive alien plant species. To avoid the spread of barnyardgrass in reused soil, its seeds must be killed before that soil is spread to new areas. We investigated the possibility of thermal control of barnyardgrass seeds using a prototype of a stationary soil steaming device. One Polish and four Norwegian seed populations were examined for thermal sensitivity. To mimic a natural range in seed moisture content, dried seeds were moistened for 0, 12, 24, or 48 h before steaming. To find effective soil temperatures and whether exposure duration is important, we tested target soil temperatures in the range 60 to 99 C at an exposure duration of 90 s (Experiment 1) and exposure durations of 30, 90, or 180 s with a target temperature of 99 C (Experiment 2). In a third experiment, we tested exposure durations of 90, 180, and 540 s at 99 C (Experiment 3). Obtaining target temperatures was challenging. For target temperatures of 60, 70, 80, and 99 C, the actual temperatures obtained were 59 to 69, 74 to 76, 77 to 83, and 94 to 99 C, respectively. After steaming treatments, seed germination was followed for 28 d in a greenhouse. Maximum soil temperature affected seed germination, but exposure duration did not. Seed premoistening was of influence but varied among temperatures and populations. The relationships between maximum soil temperature and seed germination were described by a common dose–response function. Seed germination was reduced by 50% when the maximum soil temperature reached 62 to 68 C and 90% at 76 to 86 C. For total weed control, 94 C was required in four populations, whereas 79 C was sufficient in one Norwegian population.
Forfattere
Paul Eric Aspholm Juho Vuolteenaho Hallvard Jensen Cornelya Klutsch Helena Klöckener Snorre HagenSammendrag
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Sammendrag
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Forfattere
Ammar Shihan Philippe Barre Venera Copani Rajae Kallida Liv Østrem Giorgio Testa Mark R. Norton Jean-Paul Sampoux Florence VolaireSammendrag
1. The persistence of perennial herbaceous species is threatened by increasing aridity. However, summer dormancy is a strategy conferring superior survival to grasses adapted to hot and dry summers. The role of temperature on the induction of summer dormancy was investigated in the perennial grass Dactylis glomerata to analyse the potential expression of this strategy under warmer climates. 2. We tested seven populations of D. glomerata originating from Morocco to Norway across the same latitudinal gradient in a five-site experiment. One population of the highly summer-dormant grass Poa bulbosa was used as a reference. Plants were grown from autumn in pots under full irrigation for 1 year mostly under open-air shelters. Heading date (ear emergence preceding flowering) was recorded and foliage senescence was assessed from end of spring until autumn. The maximum plant senescence under summer irrigation indicated the level of dormancy expression. Summer dormancy onset, release, expression and duration were modelled as a function of climatic variables. 3. From north to south, the duration of summer dormancy of the Mediterranean populations of D. glomerata and P. bulbosa ranged from 0 to 122 days, and 79 to 200 days, respectively. P. bulbosa was always completely dormant, while dormancy expression of D. glomerata was positively correlated with the sum of temperatures from winter onset (R2 = 0.57) and with the mean of minimum temperatures in summer (R2 = 0.73). Dormancy onset, release and duration were also positively correlated with thermal time from winter onset, while the duration of summer dormancy was longer as maximum temperatures increased. Mapping the European regions with climates allowing the expression of summer dormancy in D. glomerata showed that the potentially inductive areas for this strategy may expand in parallel with increasing summer aridity under a future climate warming scenario. 4. Synthesis. The large phenotypic variability of the expression of summer dormancy in D. glomerata was driven by temperature, suggesting that this strategy may have a greater role in higher latitudes to increase plant survival over the predicted hotter and drier summers. Leveraging this strategy for the choice and selection of suitable populations could enhance future adaptation of major perennial grasses to climate change.
Forfattere
Boban Djordjević Dejan Djurović Gordan Zec Dragana Dabić Zagorac Maja Natić Mekjell Meland Milica Fotirić AkšićSammendrag
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