Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

The Theory of Island Biogeography

There is growing recognition that classifying terrestrial plant species on the basis of their function (into 'functional types') rather than their higher taxonomic identity, is a promising way forward for tackling important ecological questions at the scale of ecosystems, landscapes or biomes. These questions include those on vegetation responses to and vegetation effects on, environmental changes (e.g. changes in climate, atmospheric chemistry, land use or other disturbances). There is also growing consensus about a shortlist of plant traits that should underlie such functional plant classifications, because they have strong predictive power of important ecosystem responses to environmental change and/or they themselves have strong impacts on ecosystem processes. The most favoured traits are those that are also relatively easy and inexpensive to measure for large numbers of plant species. Large international research efforts, promoted by the IGBP–GCTE Programme, are underway to screen predominant plant species in various ecosystems and biomes worldwide for such traits. This paper provides an international methodological protocol aimed at standardising this research effort, based on consensus among a broad group of scientists in this field. It features a practical handbook with step-by-step recipes, with relatively brief information about the ecological context, for 28 functional traits recognised as critical for tackling large-scale ecological questions.

/pdf/a-handbook-of-protocols-for-standardised-and-easy-2uo4112zhh.pdf

A handbook of protocols for standardised and easy measurement of plant functional traits worldwide

In its simplest definition, a trait is a surrogate of organismal performance, and this meaning of the term has been used by evolutionists for a long time. Over the last three decades, developments in community and ecosystem ecology have forced the concept of trait beyond these original boundaries, and trait-based approaches are now widely used in studies ranging from the level of organisms to that of ecosystems. Despite some attempts to fix the terminology, especially in plant ecology, there is currently a high degree of confusion in the use, not only of the term "trait" itself, but also in the underlying concepts it refers to. We therefore give an unambiguous definition of plant trait, with a particular emphasis on functional trait. A hierarchical perspective is proposed, extending the "performance paradigm" to plant ecology. "Functional traits" are defined as morpho-physiophenological traits which impact fitness indirectly via their effects on growth, reproduction and survival, the three components of individual performance. We finally present an integrative framework explaining how changes in trait values due to environmental variations are translated into organismal performance, and how these changes may influence processes at higher organizational levels. We argue that this can be achieved by developing "integration functions" which can be grouped into functional response (community level) and effect (ecosystem level) algorithms.

/pdf/let-the-concept-of-trait-be-functional-2ppbgwsn3s.pdf

Let the concept of trait be functional

Interactions among organisms take place within a complex milieu of abiotic and biotic processes, but we generally study them as solitary phenomena. Complex combinations of negative and positive interactions have been identified in a number of plant communities. The importance of these two processes in structuring plant communities can best be understood by comparing them along gradients of abiotic stress, consumer pressure, and among different life stages, sizes, and densities of the interacting species. Here, we discuss the roles of life stage, physiology, indirect interactions, and the physical environment on the balance of competition and facilitation in plant communities.

/pdf/competition-and-facilitation-a-synthetic-approach-to-51azsyo86c.pdf

Competition and facilitation: a synthetic approach to interactions in plant communities

http://web.clas.ufl.edu/users/mbinford/GEOXXXX_Biogeography/LiteratureForLinks/Austin_2002_spatial_prediction_species_distribution_ecology-statistics_EcolModel.pdf

Spatial prediction of species distribution: an interface between ecological theory and statistical modelling

We shall, in this last chapter, treat the floristic-sociological or Braun-Blanquet approach to classification and interpretation of communities.

The Braun-Blanquet Approach

Species Diversity in Space and Time

This study reports on small-scale changes in the distribution of plant species in a 2.5 m2 plot of grazed, species- rich Veronica spicata - Avenula pratensis grassland on shal- low, dry, nutrient-poor soil in the Great Alvar area (Stora Alvaret) of southern Oland, southeastern Sweden. Multivari- ate analysis of 0.001 m2 and 0.25 m2 quadrats within the plot showed that there is little floristic variation without any trend in the plot. Average species richness varied little throughout the study period from 1986 to 1991 with 1986 averages of 7.0 on 0.001m2, 16.3 on 0.01 m2, and 26.1 on 0.25 m2. On 0.001 m2 the highest species number found was 12, on 0.01 m2, 27. However, cumulative species richness, i.e. species number in the first year plus new species appearing in later years (aver- aged over 40 quadrats) increased over the same period, on 0.001 m2 from 7.0 in 1986 to 14.9 in 1991, and on 0.01 m2

Small-scale plant species turnover in a limestone grassland: the carousel model and some comments on the niche concept.

Two types of species pool are distinguished. The regional species pool is defined as the set of species, occurring in a certain region (here: Estonia) which are capable of coexisting in a target community. The actual species pool is defined as the set of species present in a community. Field data from 14 different vegetation types in Estonia were used. The regional pool was compiled by including from the regional flora (1) all species for which the Ellenberg indicator values did not differ more than 1.5 relative units from the community mean and (2) all indifferent species. The actual pool was compiled by careful field observations. The aim of the paper is to test the validity of two null hypotheses about the species pool. HO 1 postulates that any size of the actual species pool is equally probable in the interval between zero and the size of the regional species pool. HO 2 postulates that any value of species richness per unit area (1 m 2 ) is equally probable in the interval between zero and the size of the actual species pool. To test the strengths of the relationships Monte Carlo modelling was used. It was shown that the relation between variables was stronger than proposed by the null models (P = 0.041 for HO 1 and P = 0.002 for HO 2 ). Consequently, the size of the actual species pool is largely determined by the regional species pool, and the species richness per 1 m 2 is largely determined by the actual pool. The results are discussed in the framework of coexistence theory. The size of the regional pool is determined by evolutionary (speciation) and historical (large-scale migration) processes. The size of the actual pool depends on local-scale migration, which can be a function of isolation, successional stage, local management history, etc.

The species pool and its relation to species richness : evidence from Estonian plant communities

. The concept of species pool is reviewed. It is suggested to maintain the terms regional pool and local pool but replace actual pool by community pool. The regional and local pool are considered as selections from the regional and local flora based on ecological similarity. It is also suggested to include in the community pool a selection of species present only as diaspores in the diaspore bank (including diaspores from the seed rain), the selection being based on the same ecological criteria.



Four approaches to determine the species pool are discussed: ecological, functional and phytosociological similarity, and an experimental approach. The phytosociological approach appears to be promising. The species pool is elaborated as a fuzzy set in the sense that each species of a community or a local or regional flora is a member of any community, local or regional species pool with different degrees of membership. This membership is defined as a probability of a species to become part of the community pool of a target community which is a function of the ecological (environmen-tal/functional/phytosociological) similarity of the species with the target community; the shortness of the distance of its nearest populations, the frequency/abundance, the dispersal capacity, the actual presence of dispersal mechanisms, the germinability of newly arrived diaspores, and the longevity of seeds (viability) in the diaspore bank.



The information on species pools is needed for designing experiments where the number of species in a community is to be manipulated, for instance in restoration management.

Eddy van der Maarel

Papers

The Braun-Blanquet Approach

Species Diversity in Space and Time

Small-scale plant species turnover in a limestone grassland: the carousel model and some comments on the niche concept.

The species pool and its relation to species richness : evidence from Estonian plant communities

Species pool: the concept, its determination and significance for community restoration.