When confronted with an adaptive challenge, such as extreme temperature, closely related species frequently evolve similar phenotypes using the same genes. Although such repeated evolution is thought to be less likely in highly polygenic traits and distantly related species, this has not been tested at the genome scale. We performed a population genomic study of convergent local adaptation among two distantly related species, lodgepole pine and interior spruce. We identified a suite of 47 genes, enriched for duplicated genes, with variants associated with spatial variation in temperature or cold hardiness in both species, providing evidence of convergent local adaptation despite 140 million years of separate evolution. These results show that adaptation to climate can be genetically constrained, with certain key genes playing nonredundant roles.
We investigated adaptation to climate in populations of two widespread tree species across a range of contrasting environments in western Canada. In a series of common garden experiments, bud phenology, cold hardiness, and seedling growth traits were assessed for 254 populations in the interior spruce complex (Picea glauca, P. engelmannii, and their hybrids) and for 281 populations of lodgepole pine (Pinus contorta). Complex multitrait adaptations to different ecological regions such as boreal, montane, coastal, and arid environments accounted for 15–20% of the total variance. This population differentiation could be directly linked to climate variables through multivariate regression tree analysis. Our results suggest that adaptation to climate does not always correspond linearly to temperature gradients. For example, opposite trait values (e.g., early versus late budbreak) may be found in response to apparently similar cold environments (e.g., boreal and montane). Climate change adaptation strategies may therefore not always be possible through a simple shift of seed sources along environmental gradients. For the two species in this study, we identified a relatively small number of uniquely adapted populations (11 for interior spruce and nine for lodgepole pine) that may be used to manage adaptive variation under current and expected future climates.
The most common tool to predict future changes in species range are species distribution models. These models do, however, often underestimate potential future habitat, as they do not account for phenotypic plasticity and local adaptation, although being the most important processes in the response of tree populations to rapid climate change. Here, we quantify the difference in the predictions of future range for Norway spruce, by (i) deriving a classic, occurrence-based species distribution model (OccurrenceSDM), and (ii) analysing the variation in juvenile tree height and translating this to species occurrence (TraitSDM). Making use of 32 site locations of the most comprehensive European trial series that includes 1,100 provenances of Norway spruce originating from its natural and further beyond from its largely extended, artificial distribution, we fit a universal response function to quantify growth as a function of site and provenance climate. Both the OccurrenceSDM and TraitSDM show a substantial retreat towards the northern latitudes and higher elevations (−55 and −43%, respectively, by the 2080s). However, thanks to the species’ particularly high phenotypic plasticity in juvenile height growth, the decline is delayed. The TraitSDM identifies increasing summer heat paired with decreasing water availability as the main climatic variable that restricts growth, while a prolonged frost-free period enables a longer period of active growth and therefore increasing growth potential within the restricted, remaining area. Clear signals of local adaptation to climatic clines spanning the entire range are barely detectable, as they are disguised by a latitudinal cline. This cline strongly reflects population differentiation for the Baltic domain, but fails to capture the high phenotypic variation associated to the geographic heterogeneity in the Central European mountain ranges paired with the species history of postglacial migration. Still the model is used to provide recommendations of optimal provenance choice for future climate conditions. In essence, assisted migration may not decrease the predicted range decline of Norway spruce, but may help to capitalize on potential opportunities for increased growth associated with warmer climates.
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