Climate change induces multiple abiotic and biotic risks to forests and forestry. Risks in different spatial and temporal scales must be considered to ensure preconditions for sustainable ...multifunctional management of forests for different ecosystem services. For this purpose, the present review article summarizes the most recent findings on major abiotic and biotic risks to boreal forests in Finland under the current and changing climate, with the focus on windstorms, heavy snow loading, drought and forest fires and major insect pests and pathogens of trees. In general, the forest growth is projected to increase mainly in northern Finland. In the south, the growing conditions may become suboptimal, particularly for Norway spruce. Although the wind climate does not change remarkably, wind damage risk will increase especially in the south, because of the shortening of the soil frost period. The risk of snow damage is anticipated to increase in the north and decrease in the south. Increasing drought in summer will boost the risk of large‐scale forest fires. Also, the warmer climate increases the risk of bark beetle outbreaks and the wood decay by Heterobasidion root rot in coniferous forests. The probability of detrimental cascading events, such as those caused by a large‐scale wind damage followed by a widespread bark beetle outbreak, will increase remarkably in the future. Therefore, the simultaneous consideration of the biotic and abiotic risks is essential.
In Finland, projected climate change acts to increase forest growth by the mid‐21st century, particularly in the northern parts of the country. Nonetheless, in the south, the growing conditions may become suboptimal for Norway spruce due to drought and excessively high temperatures. Biotic damages, mainly caused by Spruce bark beetles and Heterobasidions, are anticipated to increase in southern Finland. Abiotic disturbances due to windstorms, drought and forest fires will be exacerbated especially in the south with snow damages in the north. Climate change likewise increases detrimental cascading events, for example, large‐scale wind damages followed by a widespread bark beetle outbreak.
Secondary organic aerosols (SOA) forms a major fraction of organic aerosols in the atmosphere. Knowledge of SOA properties that affect their dynamics in the atmosphere is needed for improving climate ...models. By combining experimental and modeling techniques, we investigated the factors controlling SOA evaporation under different humidity conditions. Our experiments support the conclusion of particle phase diffusivity limiting the evaporation under dry conditions. Viscosity of particles at dry conditions was estimated to increase several orders of magnitude during evaporation, up to 109 Pa s. However, at atmospherically relevant relative humidity and time scales, our results show that diffusion limitations may have a minor effect on evaporation of the studied α‐pinene SOA particles. Based on previous studies and our model simulations, we suggest that, in warm environments dominated by biogenic emissions, the major uncertainty in models describing the SOA particle evaporation is related to the volatility of SOA constituents.
Key Points
Evaporation of secondary organic aerosol from α‐pinene ozonolysis was studied under different relative humidity
At dry conditions the evaporation was likely slowed down by diffusion limitations resulting from viscosity of the particles
At atmospherically relevant relative humidity, diffusion limitations had a minor effect on evaporation of the particles
Aims
Primary forests are critical for forest biodiversity and provide key ecosystem services. In Europe, these forests are particularly scarce and it is unclear whether they are sufficiently ...protected. Here we aim to: (a) understand whether extant primary forests are representative of the range of naturally occurring forest types, (b) identify forest types which host enough primary forest under strict protection to meet conservation targets and (c) highlight areas where restoration is needed and feasible.
Location
Europe.
Methods
We combined a unique geodatabase of primary forests with maps of forest cover, potential natural vegetation, biogeographic regions and protected areas to quantify the proportion of extant primary forest across Europe's forest types and to identify gaps in protection. Using spatial predictions of primary forest locations to account for underreporting of primary forests, we then highlighted areas where restoration could complement protection.
Results
We found a substantial bias in primary forest distribution across forest types. Of the 54 forest types we assessed, six had no primary forest at all, and in two‐thirds of forest types, less than 1% of forest was primary. Even if generally protected, only ten forest types had more than half of their primary forests strictly protected. Protecting all documented primary forests requires expanding the protected area networks by 1,132 km2 (19,194 km2 when including also predicted primary forests). Encouragingly, large areas of non‐primary forest existed inside protected areas for most types, thus presenting restoration opportunities.
Main conclusion
Europe's primary forests are in a perilous state, as also acknowledged by EU's “Biodiversity Strategy for 2030.” Yet, there are considerable opportunities for ensuring better protection and restoring primary forest structure, composition and functioning, at least partially. We advocate integrated policy reforms that explicitly account for the irreplaceable nature of primary forests and ramp up protection and restoration efforts alike.
As the development of the eight‐toothed spruce bark beetle Ips typographus is temperature‐dependent, climate change may encourage development of its additional generations per year and facilitate ...mass outbreaks further north than previously known.
The aim of the study was to analyse historical changes in effective temperature sums (ETSs) and early season swarming weather for I. typographus in different forest zones of European Russia between 1960 and 2016. The difference in ETSs was analysed with linear regression using daily temperature data from the 30 meteorological stations. Historical data regarding the location of I. typographus outbreaks were examined and changes in their distribution during the entire study period were analysed.
There was a substantial increase in ETSs, especially in the latter half of the study period. Increased ETSs coincided with more favourable conditions for swarming of I. typographus. Areas with favourable ETSs for the complete development of bivoltine populations of I. typographus (>1500 DD) shifted northwards on average 450 km during the entire study period.
The northward shift of ETSs may enhance the transition from univoltine to bivoltine life cycles of I. typographus in the south and middle taiga and from bivoltine to trivoltine life cycles in conifer‐broadleaf forests.
The adaptation of different species to warming temperatures has been increasingly studied. Moose (Alces alces) is the largest of the ungulate species occupying the northern latitudes across the ...globe, and in Finland it is the most important game species. It is very well adapted to severe cold temperatures, but has a relatively low tolerance to warm temperatures. Previous studies have documented changes in habitat use by moose due to high temperatures. In many of these studies, the used areas have been classified according to how much thermal cover they were assumed to offer based on satellite/aerial imagery data. Here, we identified the vegetation structure in the areas used by moose under different thermal conditions. For this purpose, we used airborne laser scanning (ALS) data extracted from the locations of GPS‐collared moose. This provided us with detailed information about the relationships between moose and the structure of forests it uses in different thermal conditions and we were therefore able to determine and differentiate between the canopy structures at locations occupied by moose during different thermal conditions. We also discovered a threshold beyond which moose behaviour began to change significantly: as day temperatures began to reach 20 °C and higher, the search for areas with higher and denser canopies during daytime became evident. The difference was clear when compared to habitat use at lower temperatures, and was so strong that it provides supporting evidence to previous studies, suggesting that moose are able to modify their behaviour to cope with high temperatures, but also that the species is likely to be affected by warming climate.
1. It has been predicted that temperature increases of 3.6–5.8 °C would shift the northern distribution limit of
Lymantria monacha
(Linnaeus) and
Lymantria dispar
(Linnaeus) by 500–700 km, but these ...predictions ignore the effects of minimum winter temperatures. It was hypothesised that winter cold can limit range expansion due to high egg mortality in cold temperatures.
2. The present study determined the supercooling points of overwintering eggs of these forest pests, and compared these with recent minimum winter temperatures in the areas of origin of three populations. Eggs from one
L. monacha
and one
L. dispar
population from the species' core distribution area in Germany were included, as well as
L. monacha
eggs from Finland, near the northern border of the species' distribution.
3. The median supercooling points of both species were more than 10 °C lower than the median minimum winter temperatures of their areas of origin, and the median supercooling points of Finnish and German
L. monacha
eggs did not differ significantly. The median supercooling point of German
L. monacha
eggs differed from that of German
L. dispar
eggs.
4. Previous literature on the topic is referenced, and translations of the old German and Russian sources are given. Based on these results, it is argued that the frequent claim that
L. monacha
eggs can survive cold down to −40 °C is unsupported, with a value near −30 °C being a more likely limit.
5. Winter cold alone can limit the predicted range shifts of these species to 200–300 km under 3.6–5.8 °C increase scenarios, which is less than half the value of earlier estimates.
Conservation strategies are often established without consideration of the impact of climate change. However, this impact is expected to threaten species and ecosystem persistence and to have ...dramatic effects towards the end of the 21st century. Landscape suitability for species under climate change is determined by several interacting factors including dispersal and human land use. Designing effective conservation strategies at regional scales to improve landscape suitability requires measuring the vulnerabilities of specific regions to climate change and determining their conservation capacities. Although methods for defining vulnerability categories are available, methods for doing this in a systematic, cost‐effective way have not been identified. Here, we use an ecosystem model to define the potential resilience of the Finnish forest landscape by relating its current conservation capacity to its vulnerability to climate change. In applying this framework, we take into account the responses to climate change of a broad range of red‐listed species with different niche requirements. This framework allowed us to identify four categories in which representation in the landscape varies among three IPCC emission scenarios (B1, low; A1B, intermediate; A2, high emissions): (i) susceptible (B1 = 24.7%, A1B = 26.4%, A2 = 26.2%), the most intact forest landscapes vulnerable to climate change, requiring management for heterogeneity and resilience; (ii) resilient (B1 = 2.2%, A1B = 0.5%, A2 = 0.6%), intact areas with low vulnerability that represent potential climate refugia and require conservation capacity maintenance; (iii) resistant (B1 = 6.7%, A1B = 0.8%, A2 = 1.1%), landscapes with low current conservation capacity and low vulnerability that are suitable for restoration projects; (iv) sensitive (B1 = 66.4%, A1B = 72.3%, A2 = 72.0%), low conservation capacity landscapes that are vulnerable and for which alternative conservation measures are required depending on the intensity of climate change. Our results indicate that the Finnish landscape is likely to be dominated by a very high proportion of sensitive and susceptible forest patches, thereby increasing uncertainty for landscape managers in the choice of conservation strategies.