The opportunity to reflect broadly on the accomplishments, prospects, and reach of a field may present itself relatively infrequently. Each biennial meeting of the International Biogeography Society showcases ideas solicited and developed largely during the preceding year, by individuals or teams from across the breadth of the discipline. Here, we highlight challenges, developments, and opportu...

Understanding how geography, oceanography, and climate have ultimately shaped marine biodiversity requires aligning the distributions of genetic diversity across multiple taxa. Here, we examine phylogeographic partitions in the sea against a backdrop of biogeographic provinces defined by taxonomy, endemism, and species composition. The taxonomic identities used to define biogeographic provinces...

Global changes are shaping the ecology and biogeography of marine species and their fisheries. Macroecology theory, which deals with large scale relationships between ecology and biogeography, can be used to develop models to predict the effects of global changes on marine species that in turn affect their fisheries. First, based on theories linking trophic energetics and allometric scaling of ...

Species distribution modelling (SDM), also called environmental or ecological niche modelling, has developed over the last 30 years as a widely used tool in core areas of biogeography including historical biogeography, studies diversity patterns, species ranges, ecoregional classification, conservation assessment and projecting future global change impacts. In 50th anniversary year Journal Biog...

There is hardly a region in the world where mycoheterotrophy does not occur. As far as we know, all orchid species are dependent on fungi during germination and early development and are therefore classi fi ed as initial mycoheterotrophs (Chap. 1 ). Orchidaceae have a worldwide distribution and occur in almost every terrestrial ecosystem apart from deserts and permafrosts. The distribution of f...

Anthropogenic disturbances such as fishing, mining, oil drilling, bioprospecting, warming, and acidification in the deep sea are increasing, yet generalities about deep-sea biogeography remain elusive. Owing to the lack of perceived environmental variability and geographical barriers, ranges of deep-sea species were traditionally assumed to be exceedingly large. In contrast, seamount and chemos...

Hybrid evolutionary algorithms (EAs) are effective optimization methods that combine multiple EAs. We propose several hybrid EAs by combining some recently-developed EAs with a biogeography-based hybridization strategy. We test our hybrid EAs on the continuous optimization benchmarks from the 2013 Congress on Evolutionary Computation (CEC) and on some real-world traveling salesman problems. The...

I present hardware testing of an evolutionary algorithm (EA) known as distributed biogeography based optimization (DBBO). DBBO is an extended version of biogeography based optimization (BBO). Typically, EAs require a central computer to control the evaluation of candidate solutions to some optimization problem, and to control the sharing of information between those candidate solutions. DBBO, h...

The general dynamic model of oceanic island biogeography (GDM) has added a new dimension to theoretical island biogeography in recognizing that geological processes are key drivers of the evolutionary processes of diversification and extinction within remote islands. It provides a dynamic and essentially non-equilibrium framework generating novel predictions for emergent diversity properties of...

Diadromy, broadly defined here as the regular movement between freshwater and marine habitats at some time during their lives, characterizes numerous fish and invertebrate taxa. Explanations for the evolution of diadromy have focused on ecological requirements of individual taxa, rarely reflecting a comparative, phylogenetic component. When incorporated into phylogenetic studies, center of orig...