The timing of heat waves has multiyear effects on milkweed and its insect community.

Extreme heat events are becoming more frequent and intense as climate variability increases, and these events inherently vary in their timing. We predicted that the timing of a heat wave would determine its consequences for insect communities owing to temporal variation in the susceptibility of host plants to heat stress. We subjected common milkweed (Asclepias syriaca) plants to in-field experimental heat waves to investigate how the timing of heat waves, both seasonally and relative to a biotic stressor (experimental herbivory), affected their ecological consequences. We found that heat waves had multiyear, timing-specific effects on plant-insect communities. Early-season heat waves led to greater and more persistent effects on plants and herbivore communities than late-season heat waves. Heat waves following experimental herbivory had reduced consequences. Our results show that extreme climate events can have complex, lasting ecological effects beyond the year of the event-and that timing is key to understanding those effects.

The role of timing in intraspecific trait ecology.

Intraspecific trait variation has tremendous importance for species interactions and community composition. A major source of intraspecific trait variation is an organism's developmental stage; however, timing is rarely considered in studies of the ecological effects of intraspecific variation. Here, we examine the role of time in the ecology of intraspecific trait variation, focusing on plants and their interactions with other organisms. Trait variation due to differences in developmental timing has unique features and dynamics, distinguishing it from variation due to genes or the environment. When time is considered in studies of intraspecific trait ecology, the degree of variability in timing within a population becomes a key factor structuring trait-mediated ecological interactions and community processes.

Growth-defense trade-offs shape population genetic composition in an iconic forest tree species.

All organisms experience fundamental conflicts between divergent metabolic processes. In plants, a pivotal conflict occurs between allocation to growth, which accelerates resource acquisition, and to defense, which protects existing tissue against herbivory. Trade-offs between growth and defense traits are not universally observed, and a central prediction of plant evolutionary ecology is that context-dependence of these trade-offs contributes to the maintenance of intraspecific variation in defense [Züst and Agrawal, Annu. Rev. Plant Biol., 68, 513-534 (2017)]. This prediction has rarely been tested, however, and the evolutionary consequences of growth-defense trade-offs in different environments are poorly understood, especially in long-lived species [Cipollini et al., Annual Plant Reviews (Wiley, 2014), pp. 263-307]. Here we show that intraspecific trait trade-offs, even when fixed across divergent environments, interact with competition to drive natural selection of tree genotypes corresponding to their growth-defense phenotypes. Our results show that a functional trait trade-off, when coupled with environmental variation, causes real-time divergence in the genetic architecture of tree populations in an experimental setting. Specifically, competitive selection for faster growth resulted in dominance by fast-growing tree genotypes that were poorly defended against natural enemies. This outcome is a signature example of eco-evolutionary dynamics: Competitive interactions affected microevolutionary trajectories on a timescale relevant to subsequent ecological interactions [Brunner et al., Funct. Ecol. 33, 7-12 (2019)]. Eco-evolutionary drivers of tree growth and defense are thus critical to stand-level trait variation, which structures communities and ecosystems over expansive spatiotemporal scales.

Trait plasticity and trade-offs shape intra-specific variation in competitive response in a foundation tree species.

The ability to tolerate neighboring plants (i.e. degree of competitive response) is a key determinant of plant success in high-competition environments. Plant genotypes adjust their functional trait expression under high levels of competition, which may help explain intra-specific variation in competitive response. However, the relationships between traits and competitive response are not well understood, especially in trees. In this study, we investigated among-genotype associations between tree trait plasticity and competitive response. We manipulated competition intensity in experimental stands of trembling aspen (Populus tremuloides) to address the covariance between competition-induced changes in functional trait expression and aspects of competitive ability at the genotype level. Genotypic variation in the direction and magnitude of functional trait responses, especially those of crown foliar mass, phytochemistry, and leaf physiology, was associated with genotypic variation in competitive response. Traits exhibited distinct plastic responses to competition, with varying degrees of genotypic variation and covariance with other trait responses. The combination of genotypic diversity and covariance among functional traits led to tree responses to competition that were coordinated among traits yet variable among genotypes. Such relationships between tree traits and competitive success have the potential to shape stand-level trait distributions over space and time.

Associational effects of plant ontogeny on damage by a specialist insect herbivore.

Intraspecific variation in plant traits is a major cause of variation in herbivore feeding and performance. Plant defensive traits change as a plant grows, such that ontogeny may account for a substantial portion of intraspecific trait variation. We tested how the ontogenic stage of an individual plant, of an individual in the context of its neighboring plants, and of a patch of plants with mixed or uniform stages affect plant-herbivore interactions. To do this, we conducted an experimental study of the interactions between Lepidium draba, a perennial brassicaceous weed, and Plutella xylostella, a common herbivore of L. draba. We found that L. draba foliar glucosinolates, secondary metabolites often implicated in defense, decreased in concentration with plant age. In single-stage patches, herbivores performed similarly on L. draba plants of different ages. Furthermore, we found no difference in the cumulative performance of herbivores reared on mixed- or even-staged patches of L. draba. However, in mixed-stage patches, the damage experienced by a focal plant depended on the stage of neighboring plants, suggesting a preference hierarchy of the herbivore among plant stages. In our study, the amount of herbivory depended on the ontogenic neighborhood in which the plant grew. However, from the herbivore's perspective, variation in plant ontogenic stage was unimportant to its success in terms of feeding rate and final weight.

Clonal Saplings of Trembling Aspen Do Not Coordinate Defense Induction.

Induction of plant chemical defenses in response to insect feeding may be localized to the site of damage or expressed systemically, mediated by signal transduction throughout the plant. Such systemic induction processes have been widely investigated in plants with single stems, but rarely in clonal plants comprised of multiple ramets with vascular connections. For a clonal tree species such as trembling aspen (Populus tremuloides Michx), integration of induced defense within clones could be adaptive, as clones are spatially extensive and susceptible to outbreak herbivores. We used pairs of aspen saplings with shared roots, replicated from three genotypes, to determine whether defense-induction signals are communicated within clones. One ramet in each pair was subjected to a damage treatment (feeding by Lymantria dispar, followed by mechanical damage), and subsequent changes in leaf defensive chemistry were measured in both ramets. Responses to damage varied by defense type: condensed tannins (CTs) increased in damaged ramets but not in connected undamaged ramets, whereas salicinoid phenolic glycosides (SPGs) were not induced in any ramets. Genotypes varied in their levels of CTs, but not in their levels of SPGs, and responded similarly to damage treatment. These results suggest that, even with both vascular and volatile information available, young aspen ramets do not induce defenses based on signals or metabolites from other ramets. Thus, unlike other clonal plant species, aspen do not appear to coordinate defense induction within clones. Lack of coordinated early induction in aspen may be related to the function of CTs in tolerance, rather than resistance.