Concluding remarks: historical perspective and the future of island biogeography theory

By James H. Brown, Mark V. Lomolino. 2000

152 citations recorded by the source corpus.

Subfields: Ecology, Nature and Landscape Conservation, Paleontology

View Paper: https://www.semanticscholar.org/paper/2b0a4076d90934d32659a5d0e023a499dcd3ef56

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In Nature and Landscape Conservation

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Citations in the corpus

Biogeography of Iberian freshwater fishes revisited: the roles of historical versus contemporary constraints (2009, background): “In addition, explicitly linking our approach to phylogeographical data might provide missing historical information that would help to understand current regional patterns of assemblage composition ( Brown & Lomolino, 2000 ).”
The island immaturity – speciation pulse model of island evolution: an alternative to the “diversity begets diversity” model (2007, background): “Notwithstanding, many oceanic islands fail to attain their hypothetical carrying capacity as they are too young or have had too little time since some past disturbance event(s) in which to rebuild their diversity (MacArthur and Wilson 1967, Paulay 1994, Peck et al. 1999, Heaney 2000, Lomolino and B”
Island theory, matrix effects and species richness patterns in habitat fragments (2002, background): “We demonstrate that matrix effects can obscure spatial patterns that conform to the general expectations of IBT.”
A conceptual framework for studying species composition in fragments, islands and other patchy ecosystems (2002, background): “…of the variation exhibited by insular communities (Simberloff, 1974; Bramwell, 1979; Williamson, 1983; Lomolino, 1986; Whittaker, 1998) and an appreciation of the fundamental structuring influences (Abbott, 1978; Brown, 1986; Pignatti, 1995; Ricklefs & Lovette, 1999; Brown & Lomolino, 2000).”
ORIGINAL ARTICLE: A general dynamic theory of oceanic island biogeography (2008, background): “Wagner & Funk, 1995; Keast & Miller, 1996; Butaud et al., 2005; Pulvers & Colgan, 2007). Similarly, Emerson & Oromı́ (2005), in their discussion of the distribution of Canarian Tarphius, explain the absence of these beetles from the two oldest Canarian Islands (the eastern islands of Fuerteventura, ”
Inferring dispersal: a Bayesian approach to phylogeny‐based island biogeography, with special reference to the Canary Islands (2008, background): “All models start in a simplified form and are later refined by subsequent research (Brown & Lomolino, 2000).”
The Late Quaternary biogeographic histories of some Great Basin mammals (western USA) (2006, background): “…conclusion that ‘‘with the notable exception of rare obligate interdependencies, each kind of organism tends to shift its abundance and distribution individualistically as environmental changes affect its unique tolerances and requirements’’ (2004, p. 364; see also Brown and Lomolino, 2000).”
Scale and species richness: towards a general, hierarchical theory of species diversity (2001, background): “…reason why thinking about these topics often gets con¯ated, but patterns in richness and endemism are not necessarily positively related (Ceballos & Brown, 1995), e.g. remote oceanic islands are rich in endemics but impoverished in species (Whittaker, 1998; Brown & Lomolino, 2000; Heaney, 2000).”