Root traits vary as much as leaf traits and have consistent phenotypic plasticity among 14 populations of a globally widespread herb

Our understanding of plant functional trait variation among populations and how this relates to local adaptation to environmental conditions is largely shaped by above-ground traits. However, we might expect below-ground traits linked to resource acquisition and conservation to vary among populations that experience different environmental conditions. Alternatively, below-ground traits might be highly plastic in response to growing conditions, such as availability of soil resources and association with symbiont arbuscular mycorrhizal fungi (AMF). We assessed (i) the strength of among-population variation in above- and below-ground traits, (ii) the effects of growing conditions on among-population variation and (iii) whether variation among populations is linked to source environment conditions, in a globally distributed perennial Plantago lanceolata. Using seeds from 14 populations across three continents, we grew plants in a common garden experiment and measured leaf and root traits linked to resource acquisition and water conservation. We included two sets of experimental treatments (high or low water availability; with and without AMF inoculation), which enabled us to assess trait responses to growing conditions. Across treatments, the percentage of root trait variation explained by populations and continents was 9%–26%, compared to 7%–20% for leaf trait variation. From principal component analysis (PCA), the first PC axis for both root and leaf traits largely reflected plant size, while the second PC broadly captured mass allocation. Root mass allocation (PC 2) was related to mean annual temperature and mean moisture index, indicating that populations from cooler, wetter environments had longer, thinner roots. However, we found little support for a relationship between source environment and leaf trait PCs, root system size (PC1) or individual traits. Water availability and AMF inoculation effects on size were consistent among populations, with larger plants under AMF inoculation, and less mass allocation to leaves under lower water availability. Plantago lanceolata shows substantial population-level variation in a suite of root traits, but that variation is only partially linked to the source environmental variables studied. Despite considerable differences in source abiotic environments, geographically separated populations have retained a strong and similar capacity for phenotypic plasticity both above and below-ground. Read the free Plain Language Summary for this article on the Journal blog.</p

Phenotypic plasticity masks range-wide genetic differentiation for vegetative but not reproductive traits in a short-lived plant

Genetic differentiation and phenotypic plasticity jointly shape intraspecific trait variation, but their roles differ among traits. In short-lived plants, reproductive traits may be more genetically determined due to their impact on fitness, whereas vegetative traits may show higher plasticity to buffer short-term perturbations. Combining a multi-treatment greenhouse experiment with observational field data throughout the range of a widespread short-lived herb, Plantago lanceolata, we (1) disentangled genetic and plastic responses of functional traits to a set of environmental drivers and (2) assessed how genetic differentiation and plasticity shape observational trait-environment relationships. Reproductive traits showed distinct genetic differentiation that largely determined observational patterns, but only when correcting traits for differences in biomass. Vegetative traits showed higher plasticity and opposite genetic and plastic responses, masking the genetic component underlying field-observed trait variation. Our study suggests that genetic differentiation may be inferred from observational data only for the traits most closely related to fitness

Phenotypic plasticity masks range-wide genetic differentiation for vegetative but not reproductive traits in a short-lived plant

Publication history: Accepted - 19 May 2021; Published - 5 August 2021.Genetic differentiation and phenotypic plasticity jointly shape intraspecific trait variation, but their roles differ among traits. In short-lived plants, reproductive traits may be more genetically determined due to their impact on fitness, whereas vegetative traits may show higher plasticity to buffer short-term perturbations. Combining a multi-treatment greenhouse experiment with observational field data throughout the range of a widespread short-lived herb, Plantago lanceolata, we (1) disentangled genetic and plastic responses of functional traits to a set of environmental drivers and (2) assessed how genetic differentiation and plasticity shape observational trait–environment relationships. Reproductive traits showed distinct genetic differentiation that largely determined observational patterns, but only when correcting traits for differences in biomass. Vegetative traits showed higher plasticity and opposite genetic and plastic responses, masking the genetic component underlying field-observed trait variation. Our study suggests that genetic differentiation may be inferred from observational data only for the traits most closely related to fitness.Eesti Teadusagentuur, Grant/Award Number: PRG609 and PUT1409; Academy of Finland; Natural Sciences and Engineering Research Council of Canada; Science Foundation Ireland, Grant/Award Number: 15/ERCD/2803; Spanish Ministry of Science, Innovation and Universities, Grant/Award Number: IJCI-2017- 32039; European Regional Development Fun

Global urban environmental change drives adaptation in white clover

Urbanization transforms environments in ways that alter biological evolution. We examined whether urban environmental change drives parallel evolution by sampling 110,019 white clover plants from 6169 populations in 160 cities globally. Plants were assayed for a Mendelian antiherbivore defense that also affects tolerance to abiotic stressors. Urban-rural gradients were associated with the evolution of clines in defense in 47% of cities throughout the world. Variation in the strength of clines was explained by environmental changes in drought stress and vegetation cover that varied among cities. Sequencing 2074 genomes from 26 cities revealed that the evolution of urban-rural clines was best explained by adaptive evolution, but the degree of parallel adaptation varied among cities. Our results demonstrate that urbanization leads to adaptation at a global scale