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JournalISSN: 1433-8319

Perspectives in Plant Ecology Evolution and Systematics 

Elsevier BV
About: Perspectives in Plant Ecology Evolution and Systematics is an academic journal published by Elsevier BV. The journal publishes majorly in the area(s): Species richness & Population. It has an ISSN identifier of 1433-8319. Over the lifetime, 661 publications have been published receiving 38550 citations.


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TL;DR: This review proposes two main avenues to progress the understanding and prediction of the different processes occurring on the leading and trailing edge of the species' distribution in response to any global change phenomena and concludes with clear guidelines on how such modelling improvements will benefit conservation strategies in a changing world.
Abstract: Given the rate of projected environmental change for the 21st century, urgent adaptation and mitigation measures are required to slow down the on-going erosion of biodiversity. Even though increasing evidence shows that recent human-induced environmental changes have already triggered species' range shifts, changes in phenology and species' extinctions, accurate projections of species' responses to future environmental changes are more difficult to ascertain. This is problematic, since there is a growing awareness of the need to adopt proactive conservation planning measures using forecasts of species' responses to future environmental changes. There is a substantial body of literature describing and assessing the impacts of various scenarios of climate and land-use change on species' distributions. Model predictions include a wide range of assumptions and limitations that are widely acknowledged but compromise their use for developing reliable adaptation and mitigation strategies for biodiversity. Indeed, amongst the most used models, few, if any, explicitly deal with migration processes, the dynamics of population at the "trailing edge" of shifting populations, species' interactions and the interaction between the effects of climate and land-use. In this review, we propose two main avenues to progress the understanding and prediction of the different processes A occurring on the leading and trailing edge of the species' distribution in response to any global change phenomena. Deliberately focusing on plant species, we first explore the different ways to incorporate species' migration in the existing modelling approaches, given data and knowledge limitations and the dual effects of climate and land-use factors. Secondly, we explore the mechanisms and processes happening at the trailing edge of a shifting species' distribution and how to implement them into a modelling approach. We finally conclude this review with clear guidelines on how such modelling improvements will benefit conservation strategies in a changing world. (c) 2007 Rubel Foundation, ETH Zurich. Published by Elsevier GrnbH. All rights reserved.

1,134 citations

Journal ArticleDOI
TL;DR: Despite evidence of rapid forest recovery following large-scale deforestation, many degraded areas of today’s tropics will require human assistance to recover forest structure, species composition, and species interactions typical of mature tropical forests.
Abstract: Land-use history interacts with natural forces to influence the severity of disturbance events and the rate and nature of recovery processes in tropical forests. Although we are far from an integrated view of forest recovery processes, some generalizations can be made. Recovery of forest structure and composition is relatively rapid following disturbances that primarily impact forest canopies, such as hurricanes. Recovery is considerably slower following disturbances that heavily impact soils as well as aboveground vegetation, such as bulldozing, heavy or long-term grazing, and severe fires, often with long-lasting effects on species composition. The landscape matrix plays a critical role in local recovery processes. Proximity of disturbed areas to remnant forest patches promotes more rapid recovery, which depends heavily on seed dispersal. Recovery of aboveground biomass is constrained by soil fertility and texture across regions as well as across soil types within a region. Restoration of soil fertility may be a prerequisite for forest recovery on sites with severely degraded soils. Despite evidence of rapid forest recovery following large-scale deforestation, many degraded areas of today’s tropics will require human assistance to recover forest structure, species composition, and species interactions typical of mature tropical forests.

919 citations

Journal ArticleDOI
TL;DR: A two-way classification of nativeness and invasiveness that distinguishes natives, non-invasive non-natives and invasive non-Natives is offered and a simple conceptual model for cases in which high levels of environmental stress should and should not reduce invasibility is offered.
Abstract: Invasion ecology, the study of how organisms spread in habitats to which they are not native, asks both about the invasiveness of species and the invasibility of habitats: Which species are most likely to become invasive? Which habitats are most susceptible to invasion? To set the stage for considering these questions with regard to plants, we offer a two-way classification of nativeness and invasiveness that distinguishes natives, non-invasive non-natives and invasive non-natives. We then consider the current state of knowledge about invasiveness and invasibility. Despite much investigation, it has proven difficult to identify traits that consistently predict invasiveness. This may be largely because different traits favour invasiveness in different habitats. It has proven easier to identify types of habitats that are relatively invasible, such as islands and riverbanks. Factors thought to render habitats invasible include low intensities of competition, altered disturbance regimes and low levels of environmental stress, especially high resource availability. These factors probably often interact; the combination of altered disturbance with high resource availability may particularly promote invasibility. When biotic factors control invasibility, non-natives that are unlike native species may prove more invasive; the converse may also be true. We end with a simple conceptual model for cases in which high levels of environmental stress should and should not reduce invasibility. In some cases, it may be possible to manipulate stress to control biological invasions by plants.

843 citations

Journal ArticleDOI
TL;DR: The results suggest that RAPD can be a sensitive method for detection of genetic structuring according to the isolation-by-distance model, but also means that sampling strategies, as applied in individual studies, can seriously influence the resulting estimates of between-population diversity.
Abstract: A compilation of studies using RAPD markers for evaluating population differentiation resulted in 78 estimates of AMOVA-derived Φ ST and 31 estimates of Nei's G ST , as well as in 41 estimates of Nei's within-population diversity. In outcrossing taxa, estimates of between-population diversity were closely correlated with maximum geographic distance between sampled populations. A corresponding association was not found in selfing taxa. These results suggest that RAPD can be a sensitive method for detection of genetic structuring according to the isolation-by-distance model. However, it also means that sampling strategies, as applied in individual studies, can seriously influence the resulting estimates of between-population diversity. Other sampling strategies, like number of plants per population and number of scored polymorphic markers, do not seem to impart any serious artefacts. As previously verified with allozyme data, RAPD markers showed that long-lived, outcrossing, late successional taxa retain most of their genetic variability within populations. By contrast, annual, selfing and/or early successional taxa allocate most of the genetic variability among populations. Estimates for between- and within-population diversity, respectively, proved to be negatively correlated, as previously reported for allozyme data. The only major discrepancy between allozymes and RAPD markers concerns geographic range; within-population diversity was strongly affected by distributional range of the investigated species in the allozyme data but not in the RAPD data. Moreover, RAPD-based values for between-population diversity increased with increasing distributional range whereas the opposite has been reported in a large allozyme data compilation. Contrary to allozymes, RAPD marker-derived within-population diversity is probably therefore not a very good predictor of total species genetic diversity.

832 citations

Journal ArticleDOI
TL;DR: The authors need a new way to classify, describe and analyze plant allocation and plasticity because the concepts ‘trait’ and ‘plasticity’ are too broad.
Abstract: Allocation is one of the central concepts in modern ecology, providing the basis for different strategies. Allocation in plants has been conceptualized as a proportional or ratio-driven process (‘partitioning’). In this view, a plant has a given amount of resources at any point in time and it allocates these resources to different structures. But many plant ecological processes are better understood in terms of growth and size than in terms of time. In an allometric perspective, allocation is seen as a size-dependent process: allometry is the quantitative relationship between growth and allocation. Therefore most questions of allocation should be posed allometrically, not as ratios or proportions. Plants evolve allometric patterns in response to numerous selection pressures and constraints, and these patterns explain many behaviours of plant populations. In the allometric view, plasticity in allocation can be understood as a change in a plant's allometric trajectory in response to the environment. Some allocation patterns show relatively fixed allometric trajectories, varying in different environments primarily in the speed at which the trajectory is travelled, whereas other allocation patterns show great flexibility in their behaviour at a given size. Because plant growth is often indeterminate and its rate highly influenced by environmental conditions, ‘plasticity in size’ is not a meaningful concept. We need a new way to classify, describe and analyze plant allocation and plasticity because the concepts ‘trait’ and ‘plasticity’ are too broad. Three degrees of plasticity can be distinguished: (1) allometric growth (‘apparent plasticity’), (2) modular proliferation and local physiological adaptation, and (3) integrated plastic responses. Plasticity, which has evolved because it increases individual fitness, can be a disadvantage in plant production systems, where we want to optimize population, not individual, performance.

729 citations

Performance
Metrics
No. of papers from the Journal in previous years
YearPapers
202319
202235
202128
202032
201945
201844