Consumer‐resource interactions are often influenced by other species in the community, such as when neighbouring plants increase or reduce herbivory to a focal plant species (known as associational effects). The many studies on associational effects between a focal plant and some neighbour have shown that these effects can vary greatly in strength and direction. But because almost all of these studies measure associational effects from only one or two neighbour species, we know little about the actual range of associational effects that a plant species might encounter in a natural setting. This makes it difficult to determine how important effects of neighbours are in real field settings, and how associational effects might interact with competition and other processes to influence plant community composition. In this study, we used a field experiment with a focal species, We found that some neighbour species affected We found some evidence that a neighbour's associational effect was related to its biomass and phylogenetic proximity to the focal species. While neighbour species differed in their effects on physical leaf traits of focal plants (trichome density, specific leaf area, and leaf toughness), these traits did not appear to mediate the effects of neighbours on focal plant herbivory.
Closely related species are expected to have similar functional traits due to shared ancestry and phylogenetic inertia. However, few tests of this hypothesis are available for plant‐associated fungal symbionts. Fungal leaf endophytes occur in all land plants and can protect their host plant from disease by a variety of mechanisms, including by parasitizing pathogens (e.g., mycoparasitism). Here, we tested whether phylogenetic relatedness among species of
- NSF-PAR ID:
- 10446539
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Molecular Ecology
- Volume:
- 31
- Issue:
- 10
- ISSN:
- 0962-1083
- Page Range / eLocation ID:
- p. 3018-3030
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Solanum carolinense , and 11 common neighbour species to investigate how associational effects vary among many co‐occurring neighbour species and to test whether factors such as neighbour plant apparency, phylogenetic proximity to the focal species, or effects on focal plant defence traits help to explain interspecific variation in associational effect strength.S. carolinense damage and attack by specialist herbivores, but associational effects of most neighbours were weak. Associational effects increased herbivore attack on average earlier in the season (associational susceptibility) and reduced herbivore attack on average later in the season (associational resistance) relative toS. carolinense in monoculture.Synthesis . Our results suggest that the distribution of associational effect strengths in natural communities are similar to those observed for other interaction types, and that multiple mechanisms are likely acting simultaneously to shape associational effects of different neighbour species. -
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Abstract Aim Closely related species tend to resemble each other in their morphology and ecology because of shared ancestry. When exploring correlations between species traits, therefore, species cannot be treated as statistically independent. Phylogenetic comparative methods (PCMs) attempt to correct statistically for this shared evolutionary history. Almost all such approaches, however, assume that correlations between traits are constant across the tips of the tree, which we refer to as phylogenetic stationarity. We suggest that this assumption of phylogenetic stationarity might be often violated and that relationships between species traits might evolve alongside clades, for example, owing to the effects of unmeasured traits or other latent variables. Specific examples range from shifts in allometric scaling relationships between clades (e.g., basal metabolic rate and body mass in endotherms, and tree diameter and biomass in trees) to the differing relationship between leaf mass per area and shade tolerance in deciduous versus evergreen trees and shrubs.
Innovation Here, we introduce an exploratory modelling framework, phylogenetically weighted regression, which represents an extension of geographically weighted regression (GWR) used in spatial studies, to allow non‐stationarity in model parameters across a phylogenetic tree. We demonstrate our approach using empirical data on flowering time and seed mass from a well‐studied plant community in southeastern Sweden. Our model reveals strong, diverging trends across the phylogeny, including changes in the sign of the relationship between clades.
Main conclusions By allowing for phylogenetic non‐stationarity, we are able to detect shifting relationships among species traits that would be obscured in traditional PCMs; thus, we suggest that PWR might be an important exploratory tool in the search for key missing variables in comparative analyses.
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Background Fungal endophytes inhabit symptomless, living tissues of all major plant lineages to form one of earth’s most prevalent groups of symbionts. Many reproduce from senesced and/or decomposing leaves and can produce extracellular leaf-degrading enzymes, blurring the line between symbiotrophy and saprotrophy. To better understand the endophyte–saprotroph continuum we compared fungal communities and functional traits of focal strains isolated from living leaves to those isolated from leaves after senescence and decomposition, with a focus on foliage of woody plants in five biogeographic provinces ranging from tundra to subtropical scrub forest.
Methods We cultured fungi from the interior of surface-sterilized leaves that were living at the time of sampling (i.e., endophytes), leaves that were dead and were retained in plant canopies (dead leaf fungi, DLF), and fallen leaves (leaf litter fungi, LLF) from 3–4 species of woody plants in each of five sites in North America. Our sampling encompassed 18 plant species representing two families of Pinophyta and five families of Angiospermae. Diversity and composition of fungal communities within and among leaf life stages, hosts, and sites were compared using ITS-partial LSU rDNA data. We evaluated substrate use and enzyme activity by a subset of fungi isolated only from living tissues vs. fungi isolated only from non-living leaves.
Results Across the diverse biomes and plant taxa surveyed here, culturable fungi from living leaves were isolated less frequently and were less diverse than those isolated from non-living leaves. Fungal communities in living leaves also differed detectably in composition from communities in dead leaves and leaf litter within focal sites and host taxa, regardless of differential weighting of rare and abundant fungi. All focal isolates grew on cellulose, lignin, and pectin as sole carbon sources, but none displayed ligninolytic or pectinolytic activity
in vitro . Cellulolytic activity differed among fungal classes. Within Dothideomycetes, activity differed significantly between fungi from living vs. non-living leaves, but such differences were not observed in Sordariomycetes.Discussion Although some fungi with endophytic life stages clearly persist for periods of time in leaves after senescence and incorporation into leaf litter, our sampling across diverse biomes and host lineages detected consistent differences between fungal assemblages in living vs. non-living leaves, reflecting incursion by fungi from the leaf exterior after leaf death and as leaves begin to decompose. However, fungi found only in living leaves do not differ consistently in cellulolytic activity from those fungi detected thus far only in dead leaves. Future analyses should consider Basidiomycota in addition to the Ascomycota fungi evaluated here, and should explore more dimensions of functional traits and persistence to further define the endophytism-to-saprotrophy continuum.
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Abstract Forest structure and diversity can regulate tree vulnerability to damage by insects and pathogens. Past work suggests that trees with diverse neighbours should experience less leaf herbivory and less damage from specialist herbivores and diseases, and that the effect of neighbourhood diversity should be strongest at small spatial scales.
In an early stage temperate tree diversity experiment, we monitored damage from leaf removing herbivores, specialist (gallers and leaf miners) herbivores, and two specialist fungal diseases (maple leaf anthracnose and cedar apple gall rust) over 3 years. The experimental design included treatments that varied independently in phylogenetic and functional diversity and we made our analyses across four spatial scales (1–16 m2).
Neighborhood diversity simultaneously increased leaf removal for some species, decreased it for others, and had no effect on yet others. Height apparency—the difference between a focal plant’s height and its neighbours’—was the best single predictor of leaf removal across species and spatial scales, but the strength and direction of its effect were also species‐specific.
Specialist pathogens and fungal foliar diseases showed signs of associational resistance and susceptibility. Oaks (
Quercus spp.) were more resistant to leaf miners and maples were more resistant to anthracnose when surrounded by diverse neighbours (associational resistance). In contrast, birches (Betula papyrifera ) were more susceptible to leaf miners and eastern red cedars (Juniperus virginiana ) were more susceptible to cedar apple gall rust (Gymnosporangium juniperi‐virginianae ) infection in diverse environments (associational susceptibility).Herbivore and pathogen damage was better predicted by community structure and diversity at small spatial scales (1 and 4 m2) than large scales (9 and 16 m2), suggesting a characteristic spatial scale for these biodiversity‐ecosystem functioning effects.
Synthesis. Humans control forest diversity through selective harvesting and planting in natural stands and plantations. Our experimental demonstration of the role of local community structure and diversity in suppressing some forms of pest and pathogen damage to trees suggests that forest management can be most effective when diversity is considered at small spatial scales and the underlying biology of particular pests, pathogens, and hosts is taken into account. Pictured here: the “galls” formed by cedar apple gall rust (Gymnosporangium juniperae‐virginiae) on eastern red cedar (Juniperus virginiana) in early spring release wind‐dispersed teleospores. Junipers showed associational susceptibility: greater susceptibility to gall rust with more diverse neighbours. -
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Abstract Plant defense against pathogens includes a range of mechanisms, including, but not limited to, genetic resistance, pathogen‐antagonizing endophytes, and pathogen competitors. The relative importance of each mechanism can be expressed in a hierarchical view of defense. Several recent studies have shown that pathogen antagonism is inconsistently expressed within the plant defense hierarchy. Our hypothesis is that the hierarchy is governed by contingency rules that determine when and where antagonists reduce plant disease severity.
Here, we investigated whether pathogen competition influences pathogen antagonism using
Populus as a model system. In three independent field experiments, we asked whether competition for leaf mesophyll cells between aMelampsora rust pathogen and a microscopic, eriophyid mite affects rust pathogen antagonism by fungal leaf endophytes. The rust pathogen has an annual, phenological disadvantage in competition with the mite because the rust pathogen must infect its secondary host in spring before infectingPopulus . We varied mite–rust competition by utilizingPopulus genotypes characterized by differential genetic resistance to the two organisms. We inoculated plants with endophytes and allowed mites and rust to infect plants naturally.Two contingency rules emerged from the three field experiments: (a) Pathogen antagonism by endophytes can be preempted by host genes for resistance that suppress pathogen development, and (b) pathogen antagonism by endophytes can secondarily be preempted by competitive exclusion of the rust by the mite.
Synthesis : Our results point to aPopulus defense hierarchy with resistance genes on top, followed by pathogen competition, and finally pathogen antagonism by endophytes. We expect these rules will help to explain the variation in pathogen antagonism that is currently attributed to context dependency.
