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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

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Sammendrag

Cuticle is the first layer protecting plants against external biotic and abiotic factors and is responsive to climatic factors as well as determined by genetic adaptations. In this study, the chemical composition of bilberry fruit cuticular wax was investigated through a latitudinal gradient from Latvia (56°N 24°E) through Finland (65°N 25°E) to northern Norway (69°N 18°E) in two seasons 2018 and 2019. Changes in the major cuticular wax compounds, including triterpenoids, fatty acids, alkanes, aldehydes, ketones, and primary alcohols, were detected by GC-MS analysis. Generally, a decreasing trend in the proportion of triterpenoids from southern to northern latitudes, accompanied with an increase in proportion of fatty acids, aldehydes, and alkanes, in bilberry fruit cuticular wax was observed. A correlation analysis between climatic factors with proportion of wax compounds indicated that temperature was the main factor affecting the cuticular wax composition in bilberries. A controlled phytotron experiment with southern and northern bilberry ecotypes confirmed the major effect of temperature on bilberry fruit cuticular wax load and composition. Elevated temperature increased wax load most in berries of northern ecotypes. The level of triterpenoids was higher, while levels of fatty acids and alkanes were lower, in wax of bilberry fruits ripened at 18°C compared to 12°C in both northern and southern ecotypes. Based on our results, it can be postulated that the predicted increase in temperature due to climate change leads to alterations in fruit cuticular wax load and composition. In northern ecotypes, the alterations were especially evident.

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Sammendrag

The morphogenetic changes of the bud meristem during floral initiation in gooseberry were examined by scanning electron microscopy. Six floral stages, similar to those reported for black currants, were identified. We also studied the environmental control of shoot growth and floral initiation of cvs. Mucurines, Pax and Xenia in two experiments in daylight phytotron compartments at 12, 18 and 24°C. Under natural daylength conditions at Ås, Norway (69°40’N), shoot growth started to decline by mid-August and ceased in early September. Cessation of growth was associated with floral initiation at 18 and 12°C, while at 24°C, only ‘Mucurines’ initiated floral primordia. Floral Stage 2 was reached by 3 September in ‘Mucurines’ and ‘Xenia’ at 18 and 12°C and nearly 2 weeks later in ‘Pax’. In a second experiment with controlled photoperiods, all cultivars ceased growing and initiated flowering in 10-h SD within 2–3 weeks, while in 20-h LD, growth continued for 8 weeks without floral initiation. Under 10-h SD conditions, all cultivars initiated flowers also at 24°C. Flowering performance in the following spring verified these results. We conclude that gooseberry is an obligatory SD plant with a critical photoperiod of 15–16 h.