The objective of this study was to assess the use of unmanned aerial vehicle (UAV) data for modelling tree density and canopy height in young boreal forests stands. The use of UAV data for such tasks can be beneficial thanks to the high resolution and reduction of the time spent in the field. This study included 29 forest stands, within which 580 clustered plots were measured in the field. An area-based approach was adopted to which random forest models were fitted using the plot data and the corresponding UAV data and then applied and validated at plot and stand level. The results were compared to those of models based on airborne laser scanning (ALS) data and those from a traditional field-assessment. The models based on UAV data showed the smallest stand-level RMSE values for mean height (0.56 m) and tree density (1175 trees ha−1). The RMSE of the tree density using UAV data was 50% smaller than what was obtained using ALS data (2355 trees ha−1). Overall, this study highlighted that the use of UAVs for the inventory of forest stands under regeneration can be beneficial both because of the high accuracy of the derived data analytics and the time saving compared to traditional field assessments.

Forest harvesting practices can potentially increase mercury runoff from catchments. A paired catchment experiment was conducted in a boreal forest in southern Norway, to test effects of forest harvest operations on i) concentrations and fluxes of methylmercury (MeHg), total mercury (HgT), nutrients and dissolved organic matter (TOC), and on ii) MeHg bioaccumulation in stream foodwebs. Thirty percent of a catchment was harvested in winter time with snow cover but no soil frost, resulting in wheel tracks and soil compaction. Pre-harvest differences included higher streamwater MeHg, HgT and TOC, and lower pH in the treated catchment compared to the reference. No significant treatment effects on concentrations of MeHg, HgT and TOC were detected, whereas concentrations of nutrients (ammonium, nitrate, phosphorus (P)) increased significantly. Estimated catchment export of nitrate and ammonium increased fourfold, as a combined effect of changed discharge and concentrations. Export of MeHg and HgT increased weakly, primarily because of an increase in discharge. Levels of MeHg in stream invertebrates mirrored differences in aquatic MeHg between the two streams, resulting in higher MeHg in biota in the harvest catchment in pre-harvest conditions. After harvest, MeHg levels in primary consumers (herbivorous stoneflies) were no longer different between the two streams, despite continued exposure to higher aqueous MeHg in the harvested catchment. Simultaneously, dietary biomarkers (δ 15 N signature, lipid-and algal fatty acid content) in the stoneflies had changed significantly, consistent with higher nutrient loadings and associated higher diet availability in the harvested stream. The results of our experiment do not support that forest management has a strong impact on catchment MeHg production. Catchment disturbance through forest harvesting may decrease MeHg in aquatic biota, because of higher stream productivity and associated higher quality of dietary sources, at least in the short-term. Other studies on catchment MeHg production to disturbance have shown a range in responses, from strong to none. So far, no factor has emerged to explain such range in responses. Predictions of forest management effects on MeHg in streamwater and aquatic food webs are hampered by limited understanding of catchment controls on MeHg production.

Past In the early twentieth century, forestry was one of the most important sectors in Norway and an agitated discussion about the perceived decline of forest resources due to over-exploitation was ongoing. To base the discussion on facts, the young state of Norway established Landsskogtakseringen – the world’s first National Forest Inventory (NFI). Field work started in 1919 and was carried out by county. Trees were recorded on 10 m wide strips with 1–5 km interspaces. Site quality and land cover categories were recorded along each strip. Results for the first county were published in 1920, and by 1930 most forests below the coniferous tree line were inventoried. The 2nd to 5th inventories followed in the years 1937–1986. As of 1954, temporary sample plot clusters on a 3 km × 3 km grid were used as sampling units. Present The current NFI grid was implemented in the 6th NFI from 1986 to 1993, when permanent plots on a 3 km × 3 km grid were established below the coniferous tree line. As of the 7th inventory in 1994, the NFI is continuous, and 1/5 of the plots are measured annually. All trees with a diameter ≥ 5 cm are recorded on circular, 250 m 2 plots. The NFI grid was expanded in 2005 to cover alpine regions with 3 km × 9 km and 9 km × 9 km grids. In 2012, the NFI grid within forest reserves was doubled along the cardinal directions. Clustered temporary plots are used periodically to facilitate county-level estimates. As of today, more than 120 variables are recorded in the NFI including bilberry cover, drainage status, deadwood, and forest health. Land-use changes are monitored and trees outside forests are recorded. Future Considerable research efforts towards the integration of remote sensing technologies enable the publication of the Norwegian Forest Resource Map since 2015, which is also used for small area estimation at the municipality level. On the analysis side, capacity and software for long term growth and yield prognosis are being developed. Furthermore, we foresee the inclusion of further variables for monitoring ecosystem services, and an increasing demand for mapped information. The relatively simple NFI design has proven to be a robust choice for satisfying steadily increasing information needs and concurrently providing consistent time series.

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In trees adapted to cold climates, conditions during autumn and winter may influence the subsequent timing of bud burst and hence tree survival during early spring frosts. We tested the effects of two temperatures during dormancy induction and mild spells (MS) during chilling on the timing of bud burst in three Picea abies (L.) Karst. provenances (58-66 degrees N). One-year-old seedlings were induced to become dormant at temperatures of 12 or 21 degrees C applied during 9 weeks of short days (12-h photoperiod). The seedlings were then moved to cold storage and given either continuous chilling at 0.7 degrees C (control), or chilling interrupted by one 14-day MS at either 8 or 12 degrees C. Interruptions with MS were staggered throughout the 175-day chilling period, resulting in 10 MS differing in date of onset. Subsets of seedlings were moved to forcing conditions (12-h photoperiod, 12 degrees C) throughout the chilling period, to assess dormancy status at different timings of the MS treatment. Finally, after 175 days of chilling, timing of bud burst was assessed in a 24-h photoperiod at 12 degrees C (control and MS-treated seedlings). The MS treatment did not significantly affect days to bud burst when given early (after 7-35 chilling days). When MS was given after 49 chilling days or later, the seedlings burst bud earlier than the controls, and the difference increased with increasing length of the chilling period given before the MS. The 12 degrees C MS treatment was more effective than the 8 degrees C MS treatment, and the difference remained constant after the seedlings had received 66 or more chilling days before the MS treatment was applied. In all provenances, a constant temperature of 21 degrees C during dormancy induction resulted in more dormant seedlings (delayed bud burst) than a constant temperature of 12 degrees C, but this did not delay the response to the MS treatment.

For trees, the ability to obtain and maintain sufficient levels of frost hardiness in late autumn, winter and spring is crucial. We report that temperatures during dormancy induction influence bud set, frost hardiness, tolerance to cold storage, timing of bud burst and spring frost hardiness in seedlings of Norway spruce (Picea abies (L.) Karst.). Bud set occurred later in 12°C than in 21°C, and later in cool nights (7°C) than in constant temperature. One weekly frost night (-2.5°C) improved frost hardiness. Cool nights reduced frost hardiness early, but improved hardiness later during cold acclimation. Buds and stems were slightly hardier in 21°C than in 12°C, while needles were clearly hardier in 12°C. Cold daytime temperature, cool nights and one weekly frost night improved cold storability (0.7°C). Seedlings receiving high daytime temperatures burst buds later, and were less injured by light frost some days after bud burst.

Spring frost may result in detrimental damage in newly planted Picea abies (L.) Karst. seedlings if their growth rhythm is not sufficiently adapted to the climatic conditions on the forest site. The aims of this study were to evaluate how bud break and spring frost hardiness were influenced by short-day (SD) treatments with different timing and different temperature regimes during bud formation. Following winter storage, frost hardiness was tested after 1, 3 and 5 weeks in forcing conditions. The SD treatment advanced bud break compared with the control seedlings. In comparison, the effects of timing and the different temperatures on bud break were small. The SD treatment improved frost hardiness in first-year needles during dehardening. The early SD treatment resulted in improved frost hardiness in first-year needles and greater root collar diameter compared with later SD treatment. To avoid a second bud flush, it is important that a critical night length is attained when the SD treatment terminates. Low temperatures following the SD treatment resulted in increased hardiness of the needles and decreased hardiness of the stems. The contrasting effect of temperature in different plant tissues demonstrates the importance of examining different tissues following freezing tests.

No abstract