Acts in what Hutchinson (1965) has called the 'ecological theatre' are played out on various scales of space and time. To understand the drama, we must view it on the appropriate scale. Plant ecologists long ago recognized the importance of sampling scale in their descriptions of the dispersion or distribution of species (e.g. Greig-Smith, 1952). However, many ecologists have behaved as if patterns and the processes that produce them are insensitive to differences in scale and have designed their studies with little explicit attention to scale. Kareiva & Andersen (1988) surveyed nearly 100 field experiments in community ecology and found that half were conducted on plots no larger than 1 m in diameter, despite considerable differences in the sizes and types of organisms studied. Investigators addressing the same questions have often conducted their studies on quite different scales. Not surprisingly, their findings have not always matched, and arguments have ensued. The disagreements among conservation biologists over the optimal design of nature reserves (see Simberloff, 1988) are at least partly due to a failure to appreciate scaling differences among organisms. Controversies about the role of competition in structuring animal communities (Schoener, 1982; Wiens, 1983, 1989) or about the degree of coevolution in communities (Connell, 1980; Roughgarden, 1983) may reflect the

https://www.jstor.org/stable/info/2389612

Spatial Scaling in Ecology

Aim Current weaknesses of diversity theory include: a failure to distinguish different biogeographical response variables under the general heading of diversity; and a general failure of ecological theory to deal adequately with geographical scale. Our aim is to articulate the case for a top-down approach to theory building, in which scale is addressed explicitly and in which different response variables are clearly distinguished. Location The article draws upon both theoretical contributions and empirical analyses from all latitudes, focusing on terrestrial ecosystems and with some bias towards (woody) plants. Methods We review current diversity theory and terminology in relation to scale of applicability. As a starting point in developing a general theory, we take the issue of geographical gradients in species richness as a main theme and evaluate the extent to which commonly cited theories are likely to operate at scales from the macro down to the local. Results A degree of confusion surrounds the use of the terms alpha, beta and gamma diversity, and the terms local, landscape and macro-scale are preferred here as a more intuitive framework. The distinction between inventory and differentiation diversity is highlighted as important as, in terms of scale of analysis, are the concepts of focus and extent. The importance of holding area constant in analysis is stressed, as is the notion that different environmental factors exhibit measurable heterogeneity at different scales. Evaluation of several of the most common diversity theories put forward for the grand clines in species richness, indicates that they can be collapsed to dynamic hypotheses based on climate or historical explanations. The importance of the many ecological/ biological mechanisms that have been proposed is evident mainly at local scales of analysis, whilst at the macro-scale they are dependent largely upon climatic controls for their operation. Local communities have often been found not to be saturated, i.e. to be non-equilibrial. This is argued, perhaps counter-intuitively, to be entirely compatible with the persistence through time of macro-scale patterns of richness that are climatically determined. The review also incorporates recent developments in macroecology, Rapoport’s rule, trade-offs, and the importance of isolation, landscape impedance and geometric constraints on richness (the mid-domain effect) in generating richness patterns; highlighting those phenomena that are contributory to the first-order climatic pattern, and those, such as the geometric constraints, that may confound or obscure these patterns. Main conclusions A general theory of diversity must necessarily cover many disparate phenomena, at various scales of analysis, and cannot therefore be expressed in a simple formula, but individual elements of this general theory may be. In particular, it appears possible to capture in a dynamic climate-based model and ‘capacity rule’, the form of the

https://www.jstor.org/stable/pdfplus/827394.pdf

Scale and species richness: towards a general, hierarchical theory of species diversity

Aim MacArthur and Wilson’s dynamic equilibrium model of island biogeography provides a powerful framework for understanding the ecological processes acting on insular populations. However, their model is known to be less successful when applied to systems and processes operating on evolutionary and geological timescales. Here, we present a general dynamic model (GDM) of oceanic island biogeography that aims to provide a general explanation of biodiversity patterns through describing the relationships between fundamental biogeographical processes – speciation, immigration, extinction – through time and in relation to island ontogeny.

Location  Analyses are presented for the Azores, Canaries, Galapagos, Marquesas and Hawaii.

Methods  We develop a theoretical argument from first principles using a series of graphical models to convey key properties and mechanisms involved in the GDM. Based on the premises (1) that emergent properties of island biotas are a function of rates of immigration, speciation and extinction, (2) that evolutionary dynamics predominate in large, remote islands, and (3) that oceanic islands are relatively short-lived landmasses showing a characteristic humped trend in carrying capacity (via island area, topographic variation, etc.) over their life span, we derive a series of predictions concerning biotic properties of oceanic islands. We test a subset of these predictions using regression analyses based largely on data sets for native species and single-island endemics (SIEs) for particular taxa from each archipelago, and using maximum island age estimates from the literature. The empirical analyses test the power of a simple model of diversity derived from the GDM: the log(Area) + Time + Time2 model (ATT2), relative to other simpler time and area models, using several diversity metrics.

Results  The ATT2 model provides a more satisfactory explanation than the alternative models evaluated (for example the standard diversity–area models) in that it fits a higher proportion of the data sets tested, although it is not always the most parsimonious solution.

Main conclusions  The theoretical model developed herein is based on the key dynamic biological processes (migration, speciation, extinction) combined with a simple but general representation of the life cycle of oceanic islands, providing a framework for explaining patterns of biodiversity, endemism and diversification on a range of oceanic archipelagos. The properties and predictions derived from the model are shown to be broadly supported (1) by the empirical analyses presented, and (2) with reference to previous phylogenetic, ecological and geological studies.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2699.2008.01892.x

ORIGINAL ARTICLE: A general dynamic theory of oceanic island biogeography

Connectivity is classically considered an emergent property of landscapes encapsulating individuals’ flows across space. However, its operational use requires a precise understanding of why and how organisms disperse. Such movements, and hence landscape connectivity, will obviously vary according to both organism properties and landscape features. We review whether landscape connectivity estimates could gain in both precision and generality by incorporating three fundamental outcomes of dispersal theory. Firstly, dispersal is a multi-causal process; its restriction to an ‘escape reaction’ to environmental unsuitability is an oversimplification, as dispersing individuals can leave excellent quality habitat patches or stay in poor-quality habitats according to the relative costs and benefits of dispersal and philopatry. Secondly, species, populations and individuals do not always react similarly to those cues that trigger dispersal, which sometimes results in contrasting dispersal strategies. Finally, dispersal is a major component of fitness and is thus under strong selective pressures, which could generate rapid adaptations of dispersal strategies. Such evolutionary responses will entail spatiotemporal variation in landscape connectivity. We thus strongly recommend the use of genetic tools to: (i) assess gene flow intensity and direction among populations in a given landscape; and (ii) accurately estimate landscape features impacting gene flow, and hence landscape connectivity. Such approaches will provide the basic data for planning corridors or stepping stones aiming at (re)connecting local populations of a given species in a given landscape. This strategy is clearly species- and landscape-specific. But we suggest that the ecological network in a given landscape could be designed by stacking up such linkages designed for several species living in different ecosystems. This procedure relies on the use of umbrella species that are representative of other species living in the same ecosystem.

/pdf/individual-dispersal-landscape-connectivity-and-ecological-f9lagjs3dp.pdf

Individual dispersal, landscape connectivity and ecological networks.

Aim Pleistocene glacial cycles reduced global sea level by up to 130 m below present levels. These changes had profound impacts on coastal marine life, including a reduction of habitable area, changes in ocean currents, and shifts in water column thermal dynamics. We provide a comprehensive review of the impact of glacial sea-level changes during the Pleistocene on tropical coastal marine life and a set of maps showing how coastlines worldwide changed during periods of low sea levels. Location We focused on coastal marine taxa within tropical latitudes, with deeper coverage of the world’s major coral reef biogeographical provinces. Methods We examined recent and historical literature that alluded to the effects of Pleistocene sea-level fluctuations in a variety of common marine clades. Data for shelf habitat area and map construction were obtained from the NOAA ETOPO1 database, with final manipulations carried out in Adobe Illustrator CS6.

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jbi.12416

Shifting seas: the impacts of Pleistocene sea‐level fluctuations on the evolution of tropical marine taxa

The study of the diversity of animals, whatever the level of biological integration considered, greatly benefits from a hierarchical view of biogeographical processes. Patterns and processes in biogeography must be considered by reference to the three scales of space, time and change which are closely interrelated. Hierarchy theory assumes that many ecological properties can be best interpreted by an investigation in other scales than by keeping only at the scale where they are observed. Six examples going from larger to smaller scales illustrate this approach. The first concerns the debate about the relations between speciation by vicariance or speciation by dispersion. The second is a demonstration of the necessity to refer to the historical development of bird faunas in order to explain modern biogeographical patterns of distribution of birds in Mediterranean forests. As a consequence of history the third example challenges the hypothesis of ecomorphological convergence of bird communities composed of unrelated taxa living in similar mediterranean bioclimates. A fourth example analyses the processes of community organization and the regulation of regional diversities of forest birds in relation to the structure and the geographical configuration of habitats. It is shown that extinction-immigration processes are very different whether the habitat is surrounded by a deep primeval forest or is an isolated woodlot. The implications of such patterns are discussed from both theoretical and practical points of view. A fifth point illustrates the role of history and man on colonization patterns and the structure of island communities. Probability of successful colonization largely depends on species-specific histories, whether the species evolved in large tracts of homogeneous habitats or in small isolated habitats. It is shown that insular patterns of mammal communities in the Mediterranean islands cannot be explained by current theories of island biogeography because all the present species have been introduced by man in the last 8000 years. Finally the consequences of modifications of the structure of insular bird communities are explored at the level of life histories of selected species. The tradeoff of such important life history traits as the timing of reproduction, the clutch size and survival values is shown to be better explained by a detailed study of local environmental conditions than by current theories of island

From Biogeography to Life History Theory: A Multithematic Approach Illustrated by the Biogeography of Vertebrates

Aim To investigate the effects of human-induced landscape changes in Mediterranean islands on the ecological and evolutionary responses of bird communities and populations. The combination of mass extinction of large mammals and massive deforestation by humans was hypothesized to produce new selection regimes to which organisms were likely to respond. Habitat selection and niche breadth have been investigated at the scale of species, and phenotypic variation at the scale of local populations.



Location  The study was carried out along habitat gradients and in habitat mosaics at different spatial scales on the island of Corsica and in areas of similar size and structure in continental France.



Methods  Two sets of gradients have been used for investigating habitat selection and niche breadth: gradients of altitude, and gradients of vegetation structure. Population studies focused on the blue tit, Cyanistes caeruleus. Large samples of breeding attempts by this species in 10 habitats provided detailed data on phenotypic variation of fitness-related traits both on Corsica and on the mainland.



Results  The extent of niche space used by birds differed substantially depending on which habitat gradient was considered. Many species have been found to contract their habitat niche along the elevation gradient on Corsica compared with the mainland, whereas all species in the vegetation gradient broadened their niche on the island. Breeding patterns of the blue tit differed considerably depending on whether they settle in deciduous oaks (Quercus humilis) or in evergreen sclerophyllous oaks (Quercus ilex). Phenotypic variation of breeding traits was much higher on the island, where more populations were correctly timed for the best breeding period than on the mainland, a pattern that is likely to result from lower dispersal of organisms on the island.



Main conclusions  The differences in observed niche breadth between the two series of habitat gradients is explained both by the species-specific ecology of the species and the human-induced environmental history of Corsica. Large-scale landscape changes provided new opportunities for island colonization by non-forest species, which are isolated as small, ‘fugitive’ local populations. In both gradients, forest species that are typical components of the Corsican bird fauna definitely expanded their niche and occupied a wider range of habitats on Corsica than on the mainland. At the population scale, landscapes included habitat patches with contrasted selection regimes, which resulted in high phenotypic variation for many fitness-related traits. Reduced dispersal of birds on the island resulted in a much higher degree of local differentiation on Corsica than on the mainland.

On humans and wildlife in Mediterranean islands

Handle everyday research tasks with reliable, citation-backed results

Your personal Research Agent to handle research tasks with citation-backed results

Popular Tasks used by Researchers

How can I help with your research?

Meet SciSpace

Get more enhanced response by uploading the PDFs you want me to reference.

No relevant PDFs in your library

SciSpace is the AI research assistant for academics. Run systematic literature reviews on 280M+ papers, and write papers with cited sources. Trusted by 1M+ students, PhDs & researchers.

SciSpace | AI for Research

Analyze PDFs

Code & Manuscripts

Funding & Grants

Literature & Patents

Medical & Clinical Data

Systematic Review

Visualize & Present

Web & Data

Build a Google Scholar-like website for your research.

Build a website

Create charts and images for your research

Create a Chart

Write a paper for submission to a journal

Draft a manuscript

Patent Search

Design eye-catching scientific posters in minutes.

Scientific Poster Generation

Systematic Literature Review

One task is running at the moment. Your messages will be shown right after.

Drag and drop or click here to browse

Loved by <highlight>1 million+</highlight> researchers

Extract a list of specific topics and their sources from unstructured text

Topics

Compare and analyze relevant papers that matches with your search

Papers

Get insights from PDFs and bookmarked papers from your library

My library

Recent searches

Try searching for:

Catch AI-generated content in scholarly and non-scholarly content

{ai} Detector

Ai Writer

Get PDF Summaries, highlighted text explanations 

Chat with PDF

Effortlessly create in-text citations and bibliographies in APA and 2,500 other formats

Citation generator

Get explanations, summaries, and answers on academic papers

Ease up your research workflow with {scispace}'s cohort of exciting AI tools

Elevate your academic writing skills and convey your ideas the way you want

Paraphraser

Explore our range of reading and writing tools

Your file is being prepared and should be ready in a few minutes. If it's a large file, it might take a bit longer. You can close this window, and we'll email you the file when it's done.

You have reached a maximum limit of <strong>{limit}</strong> columns in the table. Remove at least <strong>1</strong> column to add or create another one.

Jacques Blondel

Author Tools

Chat about Author

Papers

From Biogeography to Life History Theory: A Multithematic Approach Illustrated by the Biogeography of Vertebrates

On humans and wildlife in Mediterranean islands