Preface and acknowledgements | p. v |
Islands as Natural Laboratories | p. 1 |
The natural laboratory paradigm | p. 3 |
Island environments | p. 10 |
Types of islands | p. 10 |
Modes of origin | p. 12 |
Plate boundary islands | p. 16 |
Islands in intraplate locations | p. 20 |
Environmental changes over long timescales | p. 22 |
Changes in relative sea level-reefs, atolls, and guyots | p. 22 |
Eustatic changes in sea level | p. 24 |
Climate change on islands | p. 26 |
The developmental history of the Canaries, Hawaii, and Jamaica | p. 27 |
The physical environment of islands | p. 32 |
Topographic characteristics | p. 32 |
Climatic characteristics | p. 34 |
Water resources | p. 36 |
Tracks in the ocean | p. 37 |
Natural disturbance on islands | p. 38 |
Magnitude and frequency | p. 40 |
Disturbance from volcanism and mega-landslides | p. 41 |
Summary | p. 45 |
The biogeography of island life: biodiversity hotspots in context | p. 46 |
Introduction: the global significance of island biodiversity | p. 46 |
Species poverty | p. 49 |
Disharmony, filters, and regional biogeography | p. 50 |
Filtering effects, dispersal limits, and disharmony | p. 50 |
Biogeographical regionalism and the vicariance/dispersalism debate | p. 52 |
Macaronesia-the biogeographical affinities of the Happy Islands | p. 60 |
Endemism | p. 63 |
Neo- and palaeoendemism | p. 63 |
Endemic plants | p. 65 |
Endemic animals | p. 67 |
Cryptic and extinct island endemics: a cautionary note | p. 71 |
Summary | p. 73 |
Island Ecology | p. 75 |
Species numbers games: the macroecology of island biotas | p. 77 |
The development of the equilibrium theory of island biogeography | p. 79 |
Island species-area relationships (ISARs) | p. 81 |
Species abundance distributions | p. 82 |
The distance effect | p. 83 |
Turnover, the core model (EMIB), and its immediate derivatives | p. 84 |
Competing explanations for systematic variation in island species-area relationships | p. 87 |
Island species numbers and ISARs: what have we learnt? | p. 89 |
Area and habitat diversity | p. 89 |
Area is not always the first variable in the model | p. 90 |
Distance and species numbers | p. 91 |
Species-area relationships in remote archipelagos | p. 92 |
Scale effects and the shape of species-area relationships | p. 93 |
Species-energy theory-a step towards a more complete island species richness model? | p. 97 |
Turnover | p. 99 |
Pseudoturnover and cryptoturnover | p. 100 |
When is an island in equilibrium? | p. 101 |
The rescue effect and the effect of island area on immigration rate | p. 102 |
The path to equilibrium | p. 103 |
What causes extinctions? | p. 104 |
Summary | p. 106 |
Community assembly and dynamics | p. 107 |
Island assembly theory | p. 107 |
Assembly rules | p. 108 |
Incidence functions and tramps | p. 108 |
The dynamics of island assembly | p. 110 |
Chequerboard distributions | p. 111 |
Combination and compatibility-assembly rules for cuckoo-doves | p. 111 |
Criticisms, 'null' models, and responses | p. 113 |
Exploring incidence functions | p. 118 |
Linking island assembly patterns to habitat factors | p. 122 |
Anthropogenic experiments in island assembly: evidence of competitive effects? | p. 125 |
Nestedness | p. 126 |
Successional island ecology: first elements | p. 129 |
Krakatau-succession, dispersal structure, and hierarchies | p. 131 |
Background | p. 131 |
Community succession | p. 131 |
A dispersal-structured model of island recolonization | p. 134 |
Colonization and turnover-the dynamics of species lists | p. 136 |
The degree of organization in the Krakatau assembly process | p. 141 |
Concluding observations | p. 143 |
Summary | p. 143 |
Scale and island ecological theory: towards a new synthesis | p. 145 |
Limitations of the dynamic equilibrium model of island biogeography: a reappraisal | p. 145 |
Scale and the dynamics of island biotas | p. 147 |
Residency and hierarchical interdependency: further illustrations from Krakatau | p. 148 |
Forms of equilibria and non-equilibria | p. 150 |
Temporal variation in island carrying capacities | p. 156 |
The prevalence and implications of intense disturbance events | p. 156 |
Variation in species number in the short and medium term | p. 157 |
Long term non-equilibrium systems | p. 158 |
Implications for endemics? | p. 159 |
Future directions | p. 161 |
Summary | p. 164 |
Island Evolution | p. 165 |
Arrival and change | p. 167 |
Founder effects, genetic drift, and bottlenecks | p. 167 |
Implications of repeated founding events | p. 170 |
After the founding event: ecological responses to empty niche space | p. 172 |
Ecological release | p. 173 |
Density compensation | p. 174 |
Character displacement | p. 176 |
Sex on islands | p. 177 |
Dioecy and outcrossing | p. 177 |
Loss of flower attractiveness | p. 178 |
Anemophily | p. 178 |
Parthenogenesis | p. 178 |
Hybridization | p. 179 |
Peculiarities of pollination and dispersal networks on islands | p. 179 |
The emergence of endemic super-generalists | p. 180 |
Unusual pollinators | p. 181 |
Unusual dispersal agents | p. 181 |
Niche shifts and syndromes | p. 181 |
The loss of dispersal powers | p. 182 |
The development of woodiness in herbaceous plant lineages | p. 184 |
Size shifts in island species and the island rule | p. 186 |
Changes in fecundity and behaviour | p. 190 |
The island syndrome in rodents | p. 192 |
Summary | p. 194 |
Speciation and the island condition | p. 195 |
The species concept and its place in phylogeny | p. 195 |
The geographical context of speciation events | p. 199 |
Distributional context | p. 199 |
Locational and historical context-island or mainland change? | p. 201 |
Mechanisms of speciation | p. 202 |
Allopatric or geographical speciation | p. 202 |
Competitive speciation | p. 204 |
Polyploidy | p. 205 |
Lineage structure | p. 206 |
Summary | p. 207 |
Emergent models of island evolution | p. 208 |
Anagenesis: speciation with little or no radiation | p. 208 |
The taxon cycle | p. 209 |
Melanesian ants | p. 209 |
Caribbean birds | p. 211 |
Caribbean anolcs | p. 215 |
Evaluation | p. 217 |
Adaptive radiation | p. 217 |
Darwin's finches and the Hawaiian honeycreeper-finches | p. 219 |
Hawaiian crickets and drosophilids | p. 225 |
Adaptive radiation in plants | p. 228 |
From valley isolates to island-hopping radiations 230 Non-adaptive radiation | p. 230 |
Speciation within an archipelago | p. 230 |
Island-hopping allopatric radiations: do clades respond to islands or to habitats? | p. 233 |
Island-hopping on the grand scale | p. 237 |
Observations on the forcing factors of island evolution | p. 238 |
Variation in insidar endemism between taxa | p. 240 |
Biogeographical hierarchies and island evolutionary models | p. 245 |
Summary | p. 247 |
Islands and Conservation | p. 249 |
Island theory and conservation | p. 251 |
Islands and conservation | p. 251 |
Habitats as islands | p. 252 |
Minimum viable popidations and minimum viable areas | p. 253 |
How many individuals are needed? | p. 253 |
How big an area? | p. 257 |
Applications of incidence functions | p. 257 |
Metapopulation dynamics | p. 259 |
The core-sink model variant | p. 261 |
Deterministic extinction and colonization within metapopulations | p. 262 |
Value of the metapopulation concept | p. 263 |
Reserve configuration-the 'Single Large or Several Small' (SLOSS) debate | p. 263 |
Dealing with the leftovers | p. 266 |
Trophic level, scale, and system extent | p. 266 |
Physical changes and the hyperdynamism of fragment systems | p. 268 |
Relaxation and turnover-the evidence | p. 269 |
Succession in fragmented landscapes | p. 274 |
The implications of nestedness | p. 275 |
Edge effects | p. 276 |
Landscape effects, isolation, and corridors | p. 278 |
The benefits of wildlife corridors | p. 278 |
The benefits of isolation | p. 279 |
Corridors or isolation? | p. 281 |
Reserve systems in the landscape | p. 281 |
Species that don't stay put | p. 282 |
Does conservation biology need island theory? | p. 283 |
A non-equilibrium world? | p. 283 |
Ecological hierarchies and fragmented landscapes | p. 285 |
Climate change and reserve systems | p. 286 |
Concluding remarks: from island biogeography to countryside biogeography? | p. 287 |
Summary | p. 288 |
Anthropogenic losses and threats to island ecosystems | p. 290 |
Current extinctions in context | p. 290 |
Stochastic versus deterministic extinctions | p. 291 |
The scale of island losses globally | p. 292 |
The agencies of destruction | p. 295 |
Predation by humans | p. 295 |
Introduced species | p. 295 |
Disease | p. 300 |
Habitat degradation and loss | p. 302 |
Trends in the causes of decline | p. 302 |
A record of passage-patterns of loss across island taxa | p. 305 |
Pacific Ocean birds and the Easter Island enigma | p. 307 |
Indian Ocean birds | p. 312 |
Reptiles | p. 313 |
Caribbean land mammals | p. 314 |
Island snails | p. 315 |
Plants in peril | p. 316 |
How fragile and invasible are island ecosystems? | p. 320 |
Summary | p. 322 |
Island remedies: the conservation of island ecosystems | p. 323 |
Contemporary problems on islands | p. 323 |
Maldives: in peril because of climatic change | p. 323 |
Okino-Tori-Shima: the strategic economic importance of a rocky outcrop | p. 324 |
Nauru: the destruction of an island | p. 324 |
The Canaries: unsustainable development in a natural paradise | p. 325 |
Contemporary problems in the Galapagos: a threatened evolutionary showcase | p. 328 |
Some conservation responses | p. 329 |
Biological control-a dangerous weapon? | p. 331 |
Translocation and release programmes | p. 331 |
Protected area and species protection systems: the Canarian example | p. 333 |
Sustainable development on islands: constraints and remedies | p. 336 |
Summary | p. 340 |
Glossary | p. 342 |
References | p. 351 |
Index | p. 383 |
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