28 research outputs found

    Relative effects of disturbance on red imported fire ants and native ant species in a longleaf pine ecosystem

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    Abstract: The degree to which changes in community composition mediate the probability of colonization and spread of non-native species is not well understood, especially in animal communities. High species richness may hinder the establishment of non-native species. Distinguishing between this scenario and cases in which no

    Ant-mediated seed dispersal in a warmed world

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    Climate change affects communities both directly and indirectly via changes in interspecific interactions. One such interaction that may be altered under climate change is the ant-plant seed dispersal mutualism common in deciduous forests of eastern North America. As climatic warming alters the abundance and activity levels of ants, the potential exists for shifts in rates of ant-mediated seed dispersal. We used an experimental temperature manipulation at two sites in the eastern US (Harvard Forest in Massachusetts and Duke Forest in North Carolina) to examine the potential impacts of climatic warming on overall rates of seed dispersal (using Asarum canadense seeds) as well as species-specific rates of seed dispersal at the Duke Forest site. We also examined the relationship between ant critical thermal maxima (CTmax) and the mean seed removal temperature for each ant species. We found that seed removal rates did not change as a result of experimental warming at either study site, nor were there any changes in species-specific rates of seed dispersal. There was, however, a positive relationship between CTmax and mean seed removal temperature, whereby species with higher CTmax removed more seeds at hotter temperatures. The temperature at which seeds were removed was influenced by experimental warming as well as diurnal and day-to-day fluctuations in temperature. Taken together, our results suggest that while temperature may play a role in regulating seed removal by ants, ant plant seed-dispersal mutualisms may be more robust to climate change than currently assumed

    Author Correction: Drivers of seedling establishment success in dryland restoration efforts

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    1 Pág. Correción errata.In the version of this Article originally published, the surname of author Tina Parkhurst was incorrectly written as Schroeder. This has now been corrected.Peer reviewe

    Priority Treatment Leaves Grassland Restoration Vulnerable to Invasion

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    Priority effects can be used to promote target species during restoration. Early planting can provide an advantage over later-arriving species, increasing abundance of these early-arrivers in restored communities. However, we have limited knowledge of the indirect impacts of priority effects in restoration. In particular, we do not understand how priority effects impact non-target species. Of particular conservation concern is how these priority effects influence establishment by non-native species. We use a field-based mesocosm experiment to explore the impacts of priority effects on both target and non-target species in California grasslands. Specifically, we seeded native grasses and forbs, manipulating order of arrival by planting them at the same time, planting forbs one year before grasses, planting grasses one year before forbs, or planting each functional group alone. While our study plots were tilled and weeded for the first year, the regional species pool was heavily invaded. We found that, while early-arrival of native grasses did not promote establishment of non-native species, giving priority to native forbs ultimately left our restoration mesocosms vulnerable to invasion by non-native species. This suggests that, in some cases, establishment of non-native species may be an unintended consequence of using priority treatments as a restoration tool

    Do Dominant Ants Affect Secondary Productivity, Behavior and Diversity in a Guild of Woodland Ants?

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    The degree to which competition by dominant species shapes ecological communities remains a largely unresolved debate. In ants, unimodal dominance–richness relationships are common and suggest that dominant species, when very abundant, competitively exclude non-dominant species. However, few studies have investigated the underlying mechanisms by which dominant ants might affect coexistence and the maintenance of species richness. In this study, we first examined the relationship between the richness of non-dominant ant species and the abundance of a dominant ant species, Formica subsericea, among forest ant assemblages in the eastern US. This relationship was hump-shaped or not significant depending on the inclusion or exclusion of an influential observation. Moreover, we found only limited evidence that F. subsericea negatively affects the productivity or behavior of non-dominant ant species. For example, at the colony-level, the size and productivity of colonies of non-dominant ant species were not different when they were in close proximity to dominant ant nests than when they were away and, in fact, was associated with increased productivity in one species. Additionally, the number of foraging workers of only one non-dominant ant species was lower at food sources near than far from dominant F. subsericea nests, while the number of foragers of other species was not negatively affected. However, foraging activity of the non-dominant ant species was greater at night when F. subsericea was inactive, suggesting a potential mechanism by which some non-dominant species avoid interactions with competitively superior species. Gaining a mechanistic understanding of how patterns of community structure arise requires linking processes from colonies to communities. Our study suggests the negative effects of dominant ant species on non-dominant species may be offset by mechanisms promoting coexistence

    Dominance hierarchies are a dominant paradigm in ant ecology (Hymenoptera: Formicidae), but should they be? and what is a dominance hierarchy anyways?

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    There is a long tradition of community ecologists using interspecific dominance hierarchies as a way to explain species coexistence and community structure. However, there is considerable variation in the methods used to construct these hierarchies, how they are quantified, and how they are interpreted. In the study of ant communities, hierarchies are typically based on the outcome of aggressive encounters between species or on bait monopolization. These parameters are converted to rankings using a variety of methods ranging from calculating the proportion of fights won or baits monopolized to minimizing hierarchical reversals. However, we rarely stop to explore how dominance hierarchies relate to the spatial and temporal structure of ant communities, nor do we ask how different ranking methods quantitatively relate to one another. Here, through a review of the literature and new analyses of both published and unpublished data, we highlight some limitations of the use of dominance hierarchies, both in how they are constructed and how they are interpreted. We show that the most commonly used ranking methods can generate variation among hierarchies given the same data and that the results depend on sample size. Moreover, these ranks are not related to resource acquisition, suggesting limited ecological implications for dominance hierarchies. These limitations in the construction, analysis, and interpretation of dominance hierarchies lead us to suggest it may be time for ant ecologists to move on from dominance hierarchies.NJS was supported by the US National Science Foundation (NSF-1136703) and acknowledges a grant from the Danish National Research Foundation to the Center for Macroecology, Evolution and Climate
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