3,124 research outputs found

    Inquiries into the causes of blind wood in roses

    Get PDF

    Spatial Scaling in Model Plant Communities

    Full text link
    We present an analytically tractable variant of the voter model that provides a quantitatively accurate description of beta-diversity (two-point correlation function) in two tropical forests. The model exhibits novel scaling behavior that leads to links between ecological measures such as relative species abundance and the species area relationship.Comment: 10 pages, 3 figure

    Reconciling Niches and Neutrality in a Subalpine Temperate Forest

    Get PDF
    The Unified Neutral Theory of Biodiversity has been put forth to explain species coexistence in forests worldwide, but its assumption of species equivalence has been met with much debate. Theoretical advancements have reconciled the opposing concepts of neutral and niche theories as two ends of a continuum, improving our understanding of global patterns in diversity and community assembly. However, the relative importance of niche and neutral processes remains understudied in temperate forests. To determine the balance of niche and neutral processes in climatically limited subalpine temperate forests, we established the Utah Forest Dynamics Plot, a 13.64-ha plot comprising 27,845 stems ≥1 cm diameter at breast height (1.37 m) representing 17 species at 3100 m elevation on the Colorado Plateau. We examined the fit of niche- and neutral-based models to the species abundance distribution (SAD), and tested three underlying assumptions of neutral theory. The neutral model was a poor fit to the SAD, but we did not find the alternative model to provide a better fit. Using spatial analyses, we tested the neutral assumptions of functional equivalence, ecological equivalence, and habitat generality. Half of species analyzed were characterized by non-neutral recruitment processes, and the two most abundant species exhibited asymmetric competitive and facilitative interactions with each other. The assumption of habitat generality was strongly contradicted, with all common species having habitat preferences. We conclude niche-based processes play the dominant role in structuring subalpine forest communities, and we suggest possible explanations for variation in the relative importance of niche vs. neutral processes along ecological gradients

    Non-neutral theory of biodiversity

    Full text link
    We present a non-neutral stochastic model for the dynamics taking place in a meta-community ecosystems in presence of migration. The model provides a framework for describing the emergence of multiple ecological scenarios and behaves in two extreme limits either as the unified neutral theory of biodiversity or as the Bak-Sneppen model. Interestingly, the model shows a condensation phase transition where one species becomes the dominant one, the diversity in the ecosystems is strongly reduced and the ecosystem is non-stationary. This phase transition extend the principle of competitive exclusion to open ecosystems and might be relevant for the study of the impact of invasive species in native ecologies.Comment: 4 pages, 3 figur

    Integrating Species Traits into Species Pools

    Get PDF
    Despite decades of research on the species‐pool concept and the recent explosion of interest in trait‐based frameworks in ecology and biogeography, surprisingly little is known about how spatial and temporal changes in species‐pool functional diversity (SPFD) influence biodiversity and the processes underlying community assembly. Current trait‐based frameworks focus primarily on community assembly from a static regional species pool, without considering how spatial or temporal variation in SPFD alters the relative importance of deterministic and stochastic assembly processes. Likewise, species‐pool concepts primarily focus on how the number of species in the species pool influences local biodiversity. However, species pools with similar richness can vary substantially in functional‐trait diversity, which can strongly influence community assembly and biodiversity responses to environmental change. Here, we integrate recent advances in community ecology, trait‐based ecology, and biogeography to provide a more comprehensive framework that explicitly considers how variation in SPFD, among regions and within regions through time, influences the relative importance of community assembly processes and patterns of biodiversity. First, we provide a brief overview of the primary ecological and evolutionary processes that create differences in SPFD among regions and within regions through time. We then illustrate how SPFD may influence fundamental processes of local community assembly (dispersal, ecological drift, niche selection). Higher SPFD may increase the relative importance of deterministic community assembly when greater functional diversity in the species pool increases niche selection across environmental gradients. In contrast, lower SPFD may increase the relative importance of stochastic community assembly when high functional redundancy in the species pool increases the influence of dispersal history or ecological drift. Next, we outline experimental and observational approaches for testing the influence of SPFD on assembly processes and biodiversity. Finally, we highlight applications of this framework for restoration and conservation. This species‐pool functional diversity framework has the potential to advance our understanding of how local‐ and regional‐scale processes jointly influence patterns of biodiversity across biogeographic regions, changes in biodiversity within regions over time, and restoration outcomes and conservation efforts in ecosystems altered by environmental change

    Ecological equivalence: a realistic assumption for niche theory as a testable alternative to neutral theory

    Get PDF
    Hubbell's 2001 neutral theory unifies biodiversity and biogeography by modelling steady-state distributions of species richness and abundances across spatio-temporal scales. Accurate predictions have issued from its core premise that all species have identical vital rates. Yet no ecologist believes that species are identical in reality. Here I explain this paradox in terms of the ecological equivalence that species must achieve at their coexistence equilibrium, defined by zero net fitness for all regardless of intrinsic differences between them. I show that the distinction of realised from intrinsic vital rates is crucial to evaluating community resilience. An analysis of competitive interactions reveals how zero-sum patterns of abundance emerge for species with contrasting life-history traits as for identical species. I develop a stochastic model to simulate community assembly from a random drift of invasions sustaining the dynamics of recruitment following deaths and extinctions. Species are allocated identical intrinsic vital rates for neutral dynamics, or random intrinsic vital rates and competitive abilities for niche dynamics either on a continuous scale or between dominant-fugitive extremes. Resulting communities have steady-state distributions of the same type for more or less extremely differentiated species as for identical species. All produce negatively skewed log-normal distributions of species abundance, zero-sum relationships of total abundance to area, and Arrhenius relationships of species to area. Intrinsically identical species nevertheless support fewer total individuals, because their densities impact as strongly on each other as on themselves. Truly neutral communities have measurably lower abundance/area and higher species/abundance ratios. Neutral scenarios can be parameterized as null hypotheses for testing competitive release, which is a sure signal of niche dynamics. Ignoring the true strength of interactions between and within species risks a substantial misrepresentation of community resilience to habitat los

    Production Systems Involving Stocker Cattle and Soft Red Winter Wheat

    Get PDF
    A three year study at the Livestock and Forestry Research Station near Batesville, Arkansas evaluated production systems involving stocker cattle and soft red winter wheat. Grazing of soft red winter wheat forage from October through February followed by harvesting wheat grain or grazing through April with stocker cattle offers an alternative to conventional farming. Soft red winter wheat, when planted by September 15, produces an ample supply of high-quality forage that supports rapid growth of stocker cattle during October through April. Net income from stocker cattle averaged over 100peracre.Anormalwheatgraincropcanalsobeharvested.Thesealternativeproductionsystemscouldincreasetheagriculturalincomebyover100 per acre. A normal wheat grain crop can also be harvested. These alternative production systems could increase the agricultural income by over 75,000,000 per year if 750,000 acres of wheat are grazed
    corecore