SummaryThe evolutionary potential of long-lived species, such as forest trees, is fundamental for their local persistence under climate change (CC). Genome-environment association (GEA) analyses reveal if species in heterogeneous environments at the regional scale are under differential selection resulting in populations with potential preadaptation to CC within this area.In 79 natural Fagus sylvatica populations, neutral genetic patterns were characterized using 12 simple sequence repeat (SSR) markers, and genomic variation (144 single nucleotide polymorphisms (SNPs) out of 52 candidate genes) was related to 87 environmental predictors in the latent factor mixed model, logistic regressions and isolation by distance/environmental (IBD/IBE) tests.SSR diversity revealed relatedness at up to 150 m intertree distance but an absence of large-scale spatial genetic structure and IBE. In the GEA analyses, 16 SNPs in 10 genes responded to one or several environmental predictors and IBE, corrected for IBD, was confirmed. The GEA often reflected the proposed gene functions, including indications for adaptation to water availability and temperature.Genomic divergence and the lack of large-scale neutral genetic patterns suggest that gene flow allows the spread of advantageous alleles in adaptive genes. Thereby, adaptation processes are likely to take place in species occurring in heterogeneous environments, which might reduce their regional extinction risk under CC.
Summary 1We used the forest succession model F C to simulate Holocene treeline dynamics along an elevational transect in the Central European Alps, in order to explore the extent and cause of changes in treeline altitude and composition. 2 A temperature reconstruction independent of vegetation proxies was used to drive the model, and the simulation results were compared with Holocene pollen and macrofossil records from a nearby site close to the present-day treeline. 3 The simulation results yielded treeline fluctuations of about ± 100 m (2375-2600 m a.s.l.), confirming earlier palaeoecological studies and quantitatively corroborating the interpretation of most palaeoecologists that decadal-to centennial-scale Holocene fluctuations of pollen and plant macrofossil frequencies reflect treeline shifts rather than productivity changes alone. 4 The simulated changes in species composition and treeline position show general agreement with palaeobotanical data between 11 000 and 4500 calibrated radiocarbon years BP. In the late Holocene, however, palaeobotanical evidence indicates a distinct lowering of the treeline, while simulation projected continuous forest cover up to an altitude of 2400 m a.s.l. 5 Our results indicate that changes in temperature alone can account for changes in treeline elevation for the first half of the Holocene. The discrepancy between simulation results and palaeobotanical records since 4500 cal. BP supports the hypothesis of a strong human influence on the Alpine treeline during the late Holocene. 6 Combining palaeoecological methods with vegetation modelling can disentangle climatic effects and early human impacts on long-term vegetation dynamics. Forest succession models may not only help palaeoecologists to achieve a better understanding of the factors driving past vegetation changes, but their validation with long-term empirical data is also an important step towards applying these models to the assessment of future vegetation dynamics in a changing climate.
We investigated forest development after the cessation of management based on inventory data from six beech forest reserves in Switzerland covering nearly 40 years, using observed changes to assess the textbook understanding of natural beech forest dynamics. Specifically, we evaluated the importance of light as a driver of tree species composition, and we aimed to disentangle the role of site characteristics and past management regimes for shaping today's forest properties. Forest dynamics in the reserves showed a clear trend toward a broadening of the diameter distribution, an increase in basal area and standing dead wood, an increase in beech dominance, and a reduction of tree species diversity over time, conforming to expectations. However, the expected development of specific structural features, such as significant amounts of large living trees and snags or a small-scale mosaic of various developmental phases, appears to take longer than the time elapsed since the cessation of management. The observed loss in species richness can be attributed to decreasing light availability, as almost all species that disappeared were shade intolerant. Additionally, the shade-intolerant tree species had a characteristic bell-shaped diameter distribution in all reserves, indicating a lack of recruits, whereas shade-tolerant species had an irregular to monotonically decreasing diameter distribution, demonstrating sustained regeneration. Along the environmental gradient covered by the six reserves, abiotic factors are sufficient to explain tree species distribution, with management history not contributing additional information. This suggests that at larger scales, tree species composition is determined by abiotic factors, but historical management strategies were obviously adapted well to the species' autecological requirements. Analyses such as ours provide the foundation for refining forest management systems as well as for developing effective and target-oriented conservation strategies.
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