The literature on biological invasions has principally focused on understanding the ecological controls and consequences of invasions. Invading populations, however, often experience rapid ...evolutionary changes associated with or soon after their introduction. Ecological and evolutionary processes can, therefore, potentially interact over relatively short timescales. A number of recent studies have begun to document these interactions and their effect on short-term invasion dynamics: (1) The degree to which founder effects, drift, and inbreeding alter the genetic composition of introduced populations is mediated by migration and dispersal patterns, the population dynamics of founding populations, and life history. The genetic changes associated with founding can themselves feed back on population dynamics and life history. (2) Patterns of human-mediated dispersal and landscape change can influence the frequency and pattern of hybridization, which in turn can alter invasion dynamics. These altered invasion dynamics can influence the frequency and pattern of subsequent hybridization and introgression. (3) Strong selection can rapidly generate ecotypic specialization. Dispersal patterns, founder effects, genetic system, and life history influence the rate of local adaptation, its persistence, and its distribution in a landscape. (4) Introduced populations are subject to selection on life history traits and can serve as selective pressure on the life history traits of native populations. Life history evolution in both natives and aliens can influence ecological interactions and population dynamics, which in turn can influence the evolution of life history. Too few studies have investigated these interactions to definitively assess their overall generality or to determine how the relative interaction strength of ecology and evolution varies across taxa or ecosystems. However, the studies that do exist report interactions from a wide breadth of taxa and from all stages in the invasion process. This suggests that ecological-evolutionary interactions may have a more pervasive influence on contemporary invasion dynamics than previously appreciated, and that at least in some situations an explicit understanding of the contemporary co-influence of ecology and evolution can produce more effective and predictive control strategies.
Many population statistics describe the characteristics of populations within and among species. These are useful for describing population dynamics, understanding how environmental factors alter ...demographic patterns, testing hypotheses related to the evolution of life history characteristics and informing the effective management of populations.
In this study, we propose a population statistic: the interstage flow. The interstage flow is defined as the product of the element in the ith row, the jth column of the population projection matrix and the jth element of the normalized stable stage distribution.
The sum of the interstage flow matrix elements is equal to the population growth rate (PGR), which is the dominant eigenvalue of the population projection matrix. The interstage flow matrix elements allow decomposition of PGR into component contributions made by transitions between developmental stages.
We demonstrate the utility of interstage flow matrices using matrix population models from the COMPADRE plant matrix database. We compared interstage flows among four life history/functional groups (FGs) (semelparous herbs, iteroparous herbs, shrubs and trees) and described how PGR reflected individual transitions related to stasis, fecundity and growth. We found that the individual flows are different among FGs.
Synthesis. The proposed population statistic, the interstage flow matrix, describes the contribution of individual developmental stage transitions to the PGR. The flow of individuals between developmental stages differs in distinctive ways among different life histories and FGs. The interstage flow matrix is a valuable statistic for describing these differences.
The proposed population statistic, the interstage flow matrix, describes the contribution of individual developmental stage transitions to the population growth rate. The flow of individuals between developmental stages differs in distinctive ways among different life histories and functional groups. The interstage flow matrix is a valuable statistic for describing these differences.
Ecosystem engineering in space and time Hastings, Alan; Byers, James E; Crooks, Jeffrey A ...
Ecology letters,
February 2007, Letnik:
10, Številka:
2
Journal Article
Recenzirano
The ecosystem engineering concept focuses on how organisms physically change the abiotic environment and how this feeds back to the biota. While the concept was formally introduced a little more than ...10 years ago, the underpinning of the concept can be traced back to more than a century to the early work of Darwin. The formal application of the idea is yielding new insights into the role of species in ecosystems and many other areas of basic and applied ecology. Here we focus on how temporal, spatial and organizational scales usefully inform the roles played by ecosystem engineers and their incorporation into broader ecological contexts. Two particular, distinguishing features of ecosystem engineers are that they affect the physical space in which other species live and their direct effects can last longer than the lifetime of the organism - engineering can in essence outlive the engineer. Together, these factors identify critical considerations that need to be included in models, experimental and observational work. The ecosystem engineering concept holds particular promise in the area of ecological applications, where influence over abiotic variables and their consequent effects on biotic communities may facilitate ecological restoration and counterbalance anthropogenic influences.
It is usually assumed that pollen availability does not limit reproduction in wind-pollinated plants. Little evidence either supporting or contradicting this assumption exists, despite the importance ...of seed production to population persistence and growth. We investigated the role of pollen limitation in an invasive estuarine grass (Spartina alterniflora), with a manipulative pollen supplementation and exclusion experiment in areas of high population density and at the low-density leading edge of the invasion. We also quantified pollen deposition rates on stigmas and pollen traps along a windward to leeward gradient. We found pollen impoverishment at the low-density leading edge of a large invasion, causing an 8-fold reduction in seed set. We found 9-fold more pollen on stigmas of high-density plants than on those of low-density plants. Pollen deposition rates on stigmas and traps did not increase downwind of low-density plants but did increase down-wind of high-density plants and dropped off precipitously across a gap that lacked pollen donors. The delay of appreciable numbers of seed caused by pollen limitation persists for decades until vegetative growth coalesces plants into continuous meadows, and this Allee effect has slowed the rate of spread of the invasion.
Ecosystem engineers affect other organisms by creating, modifying, maintaining or destroying habitats. Despite widespread recognition of these often important effects, the ecosystem engineering ...concept has yet to be widely used in ecological applications. Here, we present a conceptual framework that shows how consideration of ecosystem engineers can be used to assess the likelihood of restoration of a system to a desired state, the type of changes necessary for successful restoration and how restoration efforts can be most effectively partitioned between direct human intervention and natural ecosystem engineers.
Excess nutrient loading and large-scale invasion by nonnatives are two of the most pervasive and damaging threats to the biotic and economic integrity of our estuaries. Individually, these are potent ...forces, but it is important to consider their interactive impacts as well. In this study we investigated the potential limitation of a nonnative intertidal grass, Spartina alterniflora, by nitrogen (N) in estuaries of the western United States. Nitrogen fertilization experiments were conducted in three mud-flat habitats invaded by S. alterniflora in Willapa Bay, Washington, USA, that differed in sediment N. We carried out parallel experiments in San Francisco Bay, California, USA, in three habitats invaded by hybrid Spartina (S. alterniflora × S. foliosa), in previously unvegetated mud flat, and in native S. foliosa or Salicornia virginica marshes. We found similar aboveground biomass and growth rates between habitats and estuaries, but end-of-season belowground biomass was nearly five times greater in San Francisco Bay than in Willapa Bay. In Willapa Bay, aboveground biomass was significantly correlated with sediment N content. Addition of N significantly increased aboveground biomass, stem density, and the rate of spread into uninvaded habitat (as new stems per day) in virtually all habitats in both estuaries. Belowground biomass increased in Willapa Bay only, suggesting that belowground biomass is not N limited in San Francisco Bay due to species differences, N availability, or a latitudinal difference in the response of Spartina to N additions. The relative impact of added N was greater in Willapa Bay, the estuary with lower N inputs from the watershed, than in San Francisco Bay, a highly eutrophic estuary. Nitrogen fertilization also altered the competitive interaction between hybrid Spartina and Salicornia virginica in San Francisco Bay by increasing the density and biomass of the invader and decreasing the density of the native. There was no significant effect of N on the native, Spartina foliosa. Our results indicate that excess N loading to these ecosystems enhances the vulnerability of intertidal habitats to rapid invasion by nonnative Spartina sp.
Perennial crops potentially provide a sink for atmospheric carbon. However, there is a poor understanding of how perennial crops differ in their carbon allocation patterns, and few studies have ...tested how agronomic practices such as fertilization influence long-term patterns of carbon allocation in actual production systems. In this study, we report results of a long-term field experiment that tested the individual and combined effects of organic matter incorporation and nitrogen fertilization on carbon allocation. The mature (nine-year-old) blueberry plants in this study had an average standing carbon stock of 1147gCm−2 and average annual Net Primary Production (NPP) of 523gCm−2yr−1, values that are similar to those reported for other woody crops. Forty-four percent of blueberry annual NPP was sequestered in persistent biomass, 19% was exported as harvested fruit, and 37% entered the detrital pathway. Nitrogen applied at rates typical for blueberry production throughout the span of the study had no significant effect on total plant or soil C. However, pre-planting organic matter incorporation and periodic mulching with sawdust significantly increased both soil organic matter and soil C. Pre-planting organic matter incorporation also increased total standing plant C nine years later at maturity. At the field scale, we estimate that fields receiving pre-planting organic matter incorporation would have 4.8% (4.5Mgha−1) more standing C relative to non-amended fields, although the difference is within the range of uncertainty of the estimated values. These results suggest that blueberry production can provide a valuable medium-term carbon store that is comparable in magnitude to that of temperate tree crops, but overall carbon budgets are influenced by management practices over the first decade after planting.
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•Blueberry plant NPP was 523gCm−2yr−1.•Forty-four percent of blueberry NPP was sequestered in woody biomass.•Nine-year-old fields, including soil and cover crop, sequester up to 101tCha−1.•Organic matter amendment at planting influenced carbon stocks nine years later.•Globally, we estimated that 7.8Tg C are sequestered in blueberry fields.
While well‐recognized as an important kind of ecological interaction, physical ecosystem engineering by organisms is diverse with varied consequences, presenting challenges for developing and using ...general understanding. There is also still some uncertainty as to what it is, and some skepticism that the diversity of engineering and its effects is amenable to conceptual integration and general understanding. What then, are the key cause/effect relationships and what underlies them? Here we develop, enrich and extend our extant understanding of physical ecosystem engineering into an integrated framework that exposes the essential cause/effect relationships, their underpinnings, and the interconnections that need to be understood to explain or predict engineering effects. The framework has four cause/effect relationships linking four components: 1. An engineer causes structural change; 2. Structural change causes abiotic change; 3. Structural and abiotic change cause biotic change; 4. Structural, abiotic and biotic change can feedback to the engineer. The first two relationships describe an ecosystem engineering process and abiotic dynamics, while the second two describe biotic consequence for other species and the engineer. The four relationships can be parameterized and linked using time‐indexed equations that describe engineered system dynamics. After describing the relationships we discuss the utility of the framework; how it might be enriched; and briefly how it can be used to identify intersections of ecosystem engineering with fields outside ecology.
One of the primary functions of green roofs in urban areas is to moderate rainwater runoff, and one of the major impediments to the survival of plants on an extensive green roof (EGR) is a lack of ...available water during dry periods. Runoff moderation and water storage are both influenced by the composition of the growing media. Here we present a framework for evaluating the hydrologic performance of EGR growing media and also provide hydrologic attribute data for several commonly used EGR media constituents. In this three-phase study, we: 1) measured hydrologic attributes of individual EGR media constituents, 2) predicted attributes of media mixtures using individual constituent data, and 3) tested the seven top-ranking mixtures to evaluate hydrologic performance. Hydrologic attributes included wet weight and water held at maximum retentive capacity, long-term water retention, and hydraulic conductivity. Because perlite was light in weight yet held the greatest amount of water both at its maximum retentive capacity and in the long term, media mixtures dominated by perlite were predicted to have the best overall hydrologic performance. Mixtures dominated by pumice were also predicted to perform relatively well but were heavier. Despite the slightly greater weight and slightly lower performance, pumice may be a preferred alternative to perlite because perlite is a processed constituent with greater estimated embodied energy. Results indicate that performance of mixtures can be adequately predicted using performance of individual constituents for wet weight, water held, and long-term water retention. Hydraulic conductivity was less predictable because the pore volume in mixtures can be unrelated to the pore volume of the individual constituents. The framework presented here can be used to evaluate the performance of other EGR media, and the media attribute data can be used in formulating EGR media mixtures for specific applications. In addition, the attribute data can serve as a benchmark for evaluating other EGR media. Our results underscore the need for standardization of methods for more effective comparisons of EGR substrates, and also reinforce the need to evaluate EGR components using real-world scenarios.
Several processes likely act to change the demographic rates of introduced species over time, and this changing demography could influence the optimal management of invasive populations. Optimal ...management strategies should be derived based on the demography. However, we have a poor understanding of the degree to which the demography of introduced species changes following initial introduction. We used published matrix population models of introduced plant populations to test how population growth rate and elasticity change with time since introduction. We did not find a significant relationship between population growth rate and time since introduction. However, elasticity to stasis increased while elasticity to growth decreased with time since introduction. Broadly, as time since introduction progressed the elasticities of the introduced plant populations became more similar to those that have been reported for native species. These results suggest that the optimal management strategy should be derived incorporating elasticity through time, especially when the time scope of management is long or the available demographic data were obtained in the past.
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