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Interactions between plants and insects have long fascinated scientists. While some plants rely on insects for pollination and seed dispersal, insects rely on plants for food or as a habitat. Despite extensive research investigating pair‐wise species interactions, few studies have characterized plant and insect communities simultaneously, making it unclear if diverse plant communities are generally associated with diverse insect communities. This work aims to better understand the historical and evolutionary relationships between plant and insect phylogenetic diversity (PD) on islands. We hypothesized that phylogenetically diverse plant communities (i.e., high PD) support diverse insect communities, with the relationship varying with island isolation, area, age, and latitude. Species lists for plants and insects were compiled from the published literature, and plant PD was calculated using ´standardized mean pairwise distance´ (SES.MPD) and ´standardized mean nearest taxon distance´ (SES.MNTD). For insects, PD was estimated using the number of genera, families, and orders. We found that plant diversity in evolutionary recent times (SES.MNTD) is associated with recent insect diversity (number of genera), but no relationship was found between plant and insect diversity across whole phylogenies (plant SES.MPD vs. number of insect families). Distant islands generally support high PD of plants (high SES.MPD and SES.MNTD) and insects (low number of genera). Plant and insect PD was generally high on small islands, except for plant SES.MPD revealing no relationship with island size. Insect PD was somewhat higher on young islands (low number of families), whereas there was no relationship between island age and plant PD. Plant SES.MPD was higher on high latitude islands, yet we did not find significant relationships between the latitude and the metrics of insect PD or plant SES.MNTD. These findings suggest that protecting high plant PD may also help conserve high insect PD, with a focus on small and distant islands as potential hotspots of phylogenetic diversity across multiple taxa. High plant diversity in evolutionary more recent times is significantly associated with high recent insect diversity.

Although experiments show a positive association between vascular plant and arbuscular mycorrhizal fungal (AMF) species richness, evidence from natural ecosystems is scarce. Furthermore, there is little knowledge about how AMF richness varies with belowground plant richness and biomass. We examined relationships among AMF richness, above‐ and belowground plant richness, and plant root and shoot biomass in a native North American grassland. Root‐colonizing AMF richness and belowground plant richness were detected from the same bulk root samples by 454‐sequencing of the AMF SSU rRNA and plant trnL genes. In total we detected 63 AMF taxa. Plant richness was 1.5 times greater belowground than aboveground. AMF richness was significantly positively correlated with plant species richness, and more strongly with below‐ than aboveground plant richness. Belowground plant richness was positively correlated with belowground plant biomass and total plant biomass, whereas aboveground plant richness was positively correlated only with belowground plant biomass. By contrast, AMF richness was negatively correlated with belowground and total plant biomass. Our results indicate that AMF richness and plant belowground richness are more strongly related with each other and with plant community biomass than with the plant aboveground richness measures that have been almost exclusively considered to date.

Although many studies have shown that species richness decreases from low to high latitudes (the Latitudinal Diversity Gradient), little is known about the relationship between latitude and phylogenetic diversity. Here we examine global latitudinal patterns of phylogenetic diversity using a dataset of 459 woody and 589 herbaceous plant communities. We analysed the relationships between community phylogenetic diversity, latitude, biogeographic realm and vegetation type. Using the most recent global megaphylogeny for seed plants and the standardised effect sizes of the phylogenetic diversity metrics ‘mean pairwise distance’ (SES mpd ) and ‘mean nearest taxon distance’ (SES mntd ), we found that species were more closely-related at low latitudes in woody communities. In herbaceous communities, species were more closely-related at high latitudes than at intermediate latitudes, and the strength of this effect depended on biogeographic realm and vegetation type. Possible causes of this difference are contrasting patterns of speciation and dispersal. Most woody lineages evolved in the tropics, with many gymnosperms but few angiosperms adapting to high latitudes. In contrast, the recent evolution of herbaceous lineages such as grasses in young habitat types may drive coexistence of closely-related species at high latitudes. Our results show that high species richness commonly observed at low latitudes is not associated with high phylogenetic diversity.

Functional trait differences among species are increasingly used to infer the effects of biotic and abiotic processes on species coexistence. Commonly, the trait diversity observed within communities is compared to patterns simulated in randomly generated communities based on sampling within a region. The resulting patterns of trait convergence and divergence are assumed to reveal abiotic and biotic processes, respectively. However, biotic processes such as competition can produce both trait divergence and convergence, through either excluding similar species (niche differences, divergence) or excluding dissimilar species (weaker competitor exclusion, convergence). Hence, separating biotic and abiotic processes that can produce identical patterns of trait diversity, or even patterns that neutralize each other, is not feasible with previous methods. We propose an operational framework in which the functional trait dissimilarity within communities (FDcomm) is compared to the corresponding trait dissimilarity expected from the species pool (i.e., functional species pool diversity, FDpool). FDpool includes the set of potential species for a site delimited by the operating environmental and dispersal limitation filters. By applying these filters, the resulting pattern of trait diversity is consistent with biotic processes, i.e., trait divergence (FDcomm > FDpool) indicates niche differentiation, while trait convergence (FDcomm < FDpool) indicates weaker competitor exclusion. To illustrate this framework, with its potential application and constraints, we analyzed both simulated and field data. The functional species pool framework more consistently detected the simulated trait diversity patterns than previous approaches. In the field, using data from plant communities of typical Northern European habitats in Estonia, we found that both niche-based and weaker competitor exclusion influenced community assembly, depending on the traits and community considered. In both simulated and field data, we demonstrated that only by estimating the species pool of a site is it possible to differentiate the patterns of trait dissimilarity produced by operating biotic processes. The framework, which can be applied with both functional and phylogenetic diversity, enables a reinterpretation of community assembly processes. Solving the challenge of defining an appropriate reference species pool for a site can provide a better understanding of community assembly.

Temperate calcareous grasslands are characterized by high levels of species richness at small spatial scales. Nevertheless, many species from a habitat-specific regional species pool may be absent from local communities and represent the ‘dark diversity’ of these sites. Here we investigate dry calcareous grasslands in northern Europe to determine what proportion of the habitat-specific species pool is realized at small scales (i.e. how the community completeness varies) and which mechanisms may be contributing to the relative sizes of the observed and dark diversity. We test whether the absence of particular species in potentially suitable grassland sites is a consequence of dispersal limitation and/or a low ability to tolerate stress (e.g. drought and grazing). We analysed a total of 1223 vegetation plots (1 × 1 m) from dry calcareous grasslands in Sweden, Estonia and western Russia. The species co-occurrence approach was used to estimate the dark diversity for each plot. We calculated the maximum dispersal distance for each of the 291 species in our dataset by using simple plant traits (dispersal syndrome, growth form and seed characteristics). Large seed size was used as proxy for small seed number; tall plant height and low S-strategy type scores were used to characterise low stress-tolerance. Levels of small-scale community completeness were relatively low (more species were absent than present) and varied between the grasslands in different geographic areas. Species in the dark diversity were generally characterized by shorter dispersal distances and greater seed weight (fewer seeds) than species in the observed diversity. Species within the dark diversity were generally taller and had a lower tolerance of stressful conditions.

A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been fixed in the paper.

QUESTION: How do pollen‐based functional and phylogenetic diversity help to explain post‐glacial vegetation change in relation to climate and human influence? LOCATION: Estonia and Latvia, NE Europe. METHODS: We used a data set of 1062 pollen samples from 20 sites covering the last 14 500 yrs to estimate plant richness, evenness, functional and phylogenetic diversity (community‐weighted mean and mean pair‐wise distance). We adjusted existing functional and phylogenetic diversity measures for the pollen data and tested the methods with a simulation study. The simulations showed that species‐based and pollen‐based diversity estimates were all significantly positively correlated. RESULTS: The Late Glacial (14 500–11 650 cal. yr BP) and the mid‐Holocene (8000–4000 cal. yr BP) periods showed contrasting values for most of the diversity components, and several diversity estimates were strongly associated with climate. The cold climate during the Late Glacial led to high phylogenetic diversity, and relatively low functional diversity. Climate warming during the transition from the Late Glacial to the Holocene was followed by a decrease in phylogenetic diversity but an increase in functional diversity based on plant height and seed weight. Increasing human impact in the late Holocene was associated with an increase in plant richness and decreases in functional diversity based on plant height and seed weight and in phylogenetic diversity of herbs. CONCLUSIONS: Pollen‐based functional and phylogenetic diversity provide novel insights into post‐glacial vegetation change and its drivers. Both functional and phylogenetic diversity were closely related to climatic conditions, suggesting that trait differences play an important role in long‐term community response to climate change. Our results indicate that human impact during the last two millennia has influenced functional and phylogenetic diversity negatively by suppressing plants with certain traits (functional convergence) and giving advantage to plants from certain phylogenetic lineages. We see great potential in the further development of functional and phylogenetic diversity methods for pollen data.

Numerous studies have suggested a general relationship between the degree of host specialization and body size in herbivorous animals. In insects, smaller species are usually shown to be more specialized than larger-bodied ones. Various hypotheses have attempted to explain this pattern but rigorous proof of the body size—diet breadth relationship has been lacking, primarily because the scarceness of reliable phylogenetic information has precluded formal comparative analyses. Explicitly using phylogenetic information for a group of herbivores (geometrid moths) and their host plant range, we perform a comparative analysis to study the body size—diet breadth relationship. Considering several alternative measures of body size and diet breadth, our results convincingly demonstrate without previous methodological issues—a first for any taxon—a positive association between these traits, which has implications for evaluating various central aspects of the evolutionary ecology of herbivorous insects. We additionally demonstrate how the methods used in this study can be applied in assessing hypotheses to explain the body size—diet breadth relationship. By analyzing the relationship in tree-feeders alone and finding that the positive relationship remains, the result suggests that the body size—diet breadth relationship is not solely driven by the type of host plant that species feed on.

Herbivory is ubiquitous. Despite being a potential driver of plant distribution and performance, herbivory remains largely undocumented. Some early attempts have been made to review, globally, how much leaf area is removed through insect feeding. Kozlov et al., in one of the most comprehensive reviews regarding global patterns of herbivory, have compiled published studies regarding foliar removal and sampled data on global herbivory levels using a standardized protocol. However, in the review by Kozlov et al., only 15 sampling sites, comprising 33 plant species, were evaluated in tropical areas around the globe. In Brazil, which ranks first in terms of plant biodiversity, with a total of 46,097 species, almost half (43%) being endemic, a single data point was sampled, covering only two plant species. In an attempt to increase knowledge regarding herbivory in tropical plant species and to provide the raw data needed to test general hypotheses related to plant–herbivore interactions across large spatial scales, we proposed a joint, collaborative network to evaluate tropical herbivory. This network allowed us to update and expand the data on insect herbivory in tropical and temperate plant species. Our data set, collected with a standardized protocol, covers 45 sampling sites from nine countries and includes leaf herbivory measurements of 57,239 leaves from 209 species of vascular plants belonging to 65 families from tropical and temperate regions. They expand previous data sets by including a total of 32 sampling sites from tropical areas around the globe, comprising 152 species, 146 of them being sampled in Brazil. For temperate areas, it includes 13 sampling sites, comprising 59 species. Thus, when compared to the most recent comprehensive review of insect herbivory (Kozlov et al.), our data set has increased the base of available data for the tropical plants more than 460% (from 33 to 152 species) and the Brazilian sampling was increased 7,300% (from 2 to 146 species). Data on precise levels of herbivory are presented for more than 57,000 leaves worldwide. There are no copyright restrictions. Please cite this paper when using the current data in publications; the authors request to be informed how the data is used in the publications.

Question: There are contrasting opinions about how communities assemble along a productivity gradient, particularly in relation to competitive interactions. One view is that functionally similar, and closely related species, are less likely to co-exist (limiting similarity). Alternatively, competitive exclusion may act on dissimilar species because species bearing traits associated with low competitive ability are excluded (weaker competitor exclusion). We ask if patterns of functional and phylogenetic diversity are related to changes in species diversity in response to fertility manipulations. Location: Species-rich mesophytic grassland in Estonia. Methods: The grassland has been manipulated from 2002 to 2011 to increase (fertilizer addition) and decrease productivity (sucrose addition) in small-scale (50 cm × 50 cm) plots. We linked annual increases and decreases in species diversity to changes in functional and phylogenetic diversity. We used abundance-weighted mean pair-wise functional or phylogenetic distance of all possible species pairs. Results: We found convergence in four traits (plant height, leaf distribution, lateral spread, type of reproduction) and a decrease in mean functional and phylogenetic diversity, in support of weaker competitor exclusion or habitat filtering. There was less support for limiting similarity, with divergence found for two traits associated with decreasing species diversity (leaf distribution in the sucrose treatment and lateral spread in the fertilizer treatment). Conclusions: Our results support the view that competition can lead to the exclusion of weaker competitors, rather than increasing functional and phylogenetic diversity, as expected from the principle of limiting similarity. However, multiple assembly processes, which are generally seen as mutually exclusive, are operating simultaneously, albeit on different traits and at different stages of community assembly.