Late-spring frosts (LSFs) affect the performance of plants and animals across the world’s temperate and boreal zones, but despite their ecological and economic impact on agriculture and forestry, the geographic distribution and evolutionary impact of these frost events are poorly understood. Here, we analyze LSFs between 1959 and 2017 and the resistance strategies of Northern Hemisphere woody species to infer trees’ adaptations for minimizing frost damage to their leaves and to forecast forest vulnerability under the ongoing changes in frost frequencies. Trait values on leaf-out and leaf-freezing resistance come from up to 1,500 temperate and boreal woody species cultivated in common gardens. We find that areas in which LSFs are common, such as eastern North America, harbor tree species with cautious (late-leafing) leaf-out strategies. Areas in which LSFs used to be unlikely, such as broad-leaved forests and shrublands in Europe and Asia, instead harbor opportunistic tree species (quickly reacting to warming air temperatures). LSFs in the latter regions are currently increasing, and given species’ innate resistance strategies, we estimate that ∼35% of the European and ∼26% of the Asian temperate forest area, but only ∼10% of the North American, will experience increasing late-frost damage in the future. Our findings reveal region-specific changes in the spring-frost risk that can inform decision-making in land management, forestry, agriculture, and insurance policy.
Abstract. The condition of forest ecosystems depends on the temporal and spatial pattern of management interventions and natural disturbances. Remnants of previous conditions persisting after disturbances, or ecosystem legacies, collectively comprise ecosystem memory. Ecosystem memory in turn contributes to resilience and possibilities of ecosystem reorganization following further disturbance. Understanding the role of disturbance and legacies is a prerequisite for maintaining resilience in the face of global change. Several legacy concepts discussed in the peer-reviewed literature, including disturbance, biological, soil, land-use, and silvicultural legacies, overlap in complex ways. Here, we review these established legacy concepts and propose that the new terms "material legacy" (individuals or matter, e.g., survivors, coarse woody debris, nutrients left after disturbance) and "information legacy" (adaptations to historical disturbance regimes) cut across these previous concepts and lead to a new classification of legacies. This includes six categories: material legacies with above-and belowground, and biotic and abiotic categories, and information legacies with above-and belowground categories. These six legacies are influenced by differential patterns of editing and conditioning by "legacy syndromes" that result from natural or human-manipulated disturbance regimes that can be arranged along a gradient of naturalness. This scheme is applied to a case study of hemiboreal forests in the Baltic States of Estonia, Latvia, and Lithuania, where natural disturbance, traditional clearcut silviculture, and afforestation of abandoned agricultural lands constitute the three main legacy syndromes. These legacy syndromes in turn influence forest response to management actions and constrain resilience, leading to a mosaic of natural, manipulated, and artificial (novel) ecosystems across the landscape, depending on how the legacies in each syndrome affect ecological memory.
Aim of study: The present study evaluates a set of competition indices including spatially explicit indices combined with different competitor selection approaches and non-spatially explicit competition indices. The aim was to quantify and describe the neighbouring effects on the tree diameter growth of silver birch trees.Area of study: Region throughout Estonia. Material and methods:Data from the Estonian Network of Forest Research Plots was used. After quantifying the selected indices, the best non-spatial indices and spatial indices (combined with neighbour selection methods) were separately devised into a growth model as a predictor variable to assess the ability of the diameter growth model before and after adding competition measures. To test the species-specific effect on the competition level, the superior indices were recalculated using Ellenberg's light indicators and incorporated into the diameter growth model.Main results: Statistical analyses showed that the diameter growth is a function of neighbourhood interactions and spatial indices were better growth predictors than non-spatial indices. In addition, the best selections of competitive neighbours were acquired based on the influence zone and the competition elimination angle concepts, and using Ellenberg's light values had no significant improvement in quantifying the competition effects.Research highlights: Although the best ranking spatial competition measures were superior to the best non-spatial indices, the differences were negligible.
One of the most fundamental questions in ecology is how many species inhabit the Earth. However, due to massive logistical and financial challenges and taxonomic difficulties connected to the species concept definition, the global numbers of species, including those of important and well-studied life forms such as trees, still remain largely unknown. Here, based on global ground-sourced data, we estimate the total tree species richness at global, continental, and biome levels. Our results indicate that there are ∼73,000 tree species globally, among which ∼9,000 tree species are yet to be discovered. Roughly 40% of undiscovered tree species are in South America. Moreover, almost one-third of all tree species to be discovered may be rare, with very low populations and limited spatial distribution (likely in remote tropical lowlands and mountains). These findings highlight the vulnerability of global forest biodiversity to anthropogenic changes in land use and climate, which disproportionately threaten rare species and thus, global tree richness.
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