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Ecosystem Consequences (ecosystem + consequence)

Distribution by Scientific Domains

Life Sciences	83%

Selected Abstracts

Individual, Population, Community, and Ecosystem Consequences of a Fish Invader in New Zealand Streams

CONSERVATION BIOLOGY, Issue 1 2003
Colin R. Townsend
But because invaders can have unexpected indirect effects in food webs, invasion ecologists need to integrate processes at the population level and other ecological levels. I describe a series of coordinated studies in New Zealand streams that address the effect of an exotic fish on individual behavior, population, community, and ecosystem patterns. Such case studies are important as an aid to the formulation of policy about invasions that are especially likely to become problematic. At the individual level, grazing invertebrates showed changes in behavior as a result of the introduction of brown trout ( Salmo trutta), a predator that exerts a very different selection pressure than do native fish. At the population level, trout have replaced nonmigratory galaxiid fish in some streams but not others, and have affected the distributions of crayfish and other large invertebrates. At the community level, trout have suppressed grazing pressure from invertebrates and are thus responsible for enhancing algal biomass and changing algal species composition. Finally, at the ecosystem level, essentially all annual production of invertebrates is consumed by trout ( but not by galaxiids), and algal primary productivity is six times higher in a trout stream. This leads, in turn, to an increased flux of nutrients from the water to the benthic community. The trout invasion has led to strong top-down control of community structure and ecosystem functioning via its effects on individual behavior and population distribution and abundance. Particular physiological, behavioral, and demographic traits of invaders can lead to profound ecosystem consequences that managers need to take into account. Resumen: Para desarrollar procedimientos y políticas de manejo efectivos a menudo será necesario conocer la biología de la población de especies invasoras. Sin embargo, debido a que los invasores pueden tener efectos indirectos inesperados en las redes alimenticias, ecólogos de invasión necesitan integrar procesos en la población y otros niveles ecológicos. Describo una serie de estudios coordinados en arroyos de Nueva Zelanda que enfocan el impacto de un pez exótico sobre los patrones de comportamiento individual, de la población, la comunidad y el ecosistema. Tales estudios de caso son importantes como un auxiliar para la formulación de políticas sobre invasiones que pueden ser especialmente problemáticas. Al nivel individual, los invertebrados que pastorean mostraron cambios de conducta como resultado de la introducción de la trucha café ( Salmo trutta), un depredador que ejerce una presión de selección muy diferente a la de los peces nativos. En el nivel de población, las truchas han reemplazado a peces galaxídos no migratorios en algunos arroyos pero no en otros y han afectado las distribuciones de cangrejos de río y otros invertebrados mayores. Al nivel de comunidad, las truchas han suprimido la presión de pastoreo por invertebrados y por lo tanto son responsables del incremento de la biomasa de algas y del cambio en la composición de especies de algas. Finalmente, a nivel de ecosistema, la producción anual de invertebrados esencialmente es consumida por las truchas ( pero no por galaxídos), y la productividad primaria de algas es seis veces mayor en arroyos con truchas. A su vez, esto conduce a incrementos en el flujo de nutrientes del agua hacia la comunidad béntica. La invasión de truchas ha conducido a un fuerte control de arriba hacia abajo de la estructura de la comunidad y del funcionamiento del ecosistema por medio de sus efectos sobre la conducta individual y la distribución y abundancia de la población. Las características fisiológicas, de conducta y demográficas particulares de los invasores pueden llevar a consecuencias profundas en los ecosistemas que los administradores necesitan tomar en consideración. [source]

Short and long term consequences of increases in exotic species richness on water filtration by marine invertebrates

ECOLOGY LETTERS, Issue 8 2009
Jarrett Byrnes
Abstract Although recent research has considered the consequences of global declines in the number of species, less attention has focused on the aggregate effects of regional increases in species richness as a result of human-mediated introductions. Here we examine several potential ecosystem consequences of increasing exotic species diversity of suspension feeding marine invertebrates. First, we experimentally manipulated native and non-native suspension feeder richness and measured its effect on short-term phytoplankton clearance rates. Multispecies communities all performed similarly, regardless of whether they were dominated by natives, exotics, or an even mix of the two. Individual species varied considerably in filtration rates, but non-native species often filtered less than the most similar native. Second, we determined potential changes in integrated function over time by comparing seasonal patterns of recruitment as a proxy for the ability to quickly recover filtration capacity after a disturbance. We found that exotic species have complementary seasonal phenologies both to native species and each other. Our results suggest that the consequences of local increases in species richness due to invasions may be manifest over long (annual to interannual) time scales, even when short term changes in ecosystem function are negligible. [source]

The merging of community ecology and phylogenetic biology

ECOLOGY LETTERS, Issue 7 2009
Jeannine Cavender-Bares
Abstract The increasing availability of phylogenetic data, computing power and informatics tools has facilitated a rapid expansion of studies that apply phylogenetic data and methods to community ecology. Several key areas are reviewed in which phylogenetic information helps to resolve long-standing controversies in community ecology, challenges previous assumptions, and opens new areas of investigation. In particular, studies in phylogenetic community ecology have helped to reveal the multitude of processes driving community assembly and have demonstrated the importance of evolution in the assembly process. Phylogenetic approaches have also increased understanding of the consequences of community interactions for speciation, adaptation and extinction. Finally, phylogenetic community structure and composition holds promise for predicting ecosystem processes and impacts of global change. Major challenges to advancing these areas remain. In particular, determining the extent to which ecologically relevant traits are phylogenetically conserved or convergent, and over what temporal scale, is critical to understanding the causes of community phylogenetic structure and its evolutionary and ecosystem consequences. Harnessing phylogenetic information to understand and forecast changes in diversity and dynamics of communities is a critical step in managing and restoring the Earth's biota in a time of rapid global change. [source]

Darkness visible: reflections on underground ecology

JOURNAL OF ECOLOGY, Issue 2 2005
A. H. FITTER
Summary 1Soil science and ecology have developed independently, making it difficult for ecologists to contribute to urgent current debates on the destruction of the global soil resource and its key role in the global carbon cycle. Soils are believed to be exceptionally biodiverse parts of ecosystems, a view confirmed by recent data from the UK Soil Biodiversity Programme at Sourhope, Scotland, where high diversity was a characteristic of small organisms, but not of larger ones. Explaining this difference requires knowledge that we currently lack about the basic biology and biogeography of micro-organisms. 2It seems inherently plausible that the high levels of biological diversity in soil play some part in determining the ability of soils to undertake ecosystem-level processes, such as carbon and mineral cycling. However, we lack conceptual models to address this issue, and debate about the role of biodiversity in ecosystem processes has centred around the concept of functional redundancy, and has consequently been largely semantic. More precise construction of our experimental questions is needed to advance understanding. 3These issues are well illustrated by the fungi that form arbuscular mycorrhizas, the Glomeromycota. This ancient symbiosis of plants and fungi is responsible for phosphate uptake in most land plants, and the phylum is generally held to be species-poor and non-specific, with most members readily colonizing any plant species. Molecular techniques have shown both those assumptions to be unsafe, raising questions about what factors have promoted diversification in these fungi. One source of this genetic diversity may be functional diversity. 4Specificity of the mycorrhizal interaction between plants and fungi would have important ecosystem consequences. One example would be in the control of invasiveness in introduced plant species: surprisingly, naturalized plant species in Britain are disproportionately from mycorrhizal families, suggesting that these fungi may play a role in assisting invasion. 5What emerges from an attempt to relate biodiversity and ecosystem processes in soil is our extraordinary ignorance about the organisms involved. There are fundamental questions that are now answerable with new techniques and sufficient will, such as how biodiverse are natural soils? Do microbes have biogeography? Are there rare or even endangered microbes? [source]

Detecting predator,prey relationships in the sea

JOURNAL OF FISH BIOLOGY, Issue 2003
N. K. Dulvy
Understanding the strength and diversity of predator-prey interactions among species is essential to understand ecosystem consequences of population-level variation. Directly quantifying the predatory behaviour of wild fishes at large spatial scales (>100 m) in the open sea is fraught with difficulties. To date the only empirical approach has been to search for correlations in the abundance of predators and their putative prey. As an example we use this approach to search for predators of the keystone crown-of-thorns starfish. We show that this approach is unlikely to detect predator,prey linkages because the theoretical relationship is non-linear, resulting in multiple possible prey responses for single given predator abundance. Instead we suggest some indication of the strength and ecosystem importance of a predator,prey relationship can be gained by using the abundance of both predators and their putative prey to parameterize functional response models. [source]