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Insular biogeography [1] or island biogeography is a field within biogeography that examines the factors that affect the species richness and diversification of isolated natural communities. The theory was originally developed to explain the pattern of the species–area relationship occurring in oceanic islands.
Garganornis ballmanni, a very large fossil goose from the Gargano and Scontrone islands of the Late Miocene. Foster's rule, also known as the island rule or the island effect, is an ecogeographical rule in evolutionary biology stating that members of a species get smaller or bigger depending on the resources available in the environment.
The Theory of Island Biogeography is a 1967 book by the ecologist Robert MacArthur and the biologist Edward O. Wilson. [1] It is widely regarded as a seminal work in island biogeography and ecology. The Princeton University Press reprinted the book in 2001 as a part of the "Princeton Landmarks in Biology" series. [1]
Size comparison of the giant gymnure (moonrat) Deinogalerix from the Late Miocene of Gargano, Italy, with a European hedgehog. Island gigantism, or insular gigantism, is a biological phenomenon in which the size of an animal species isolated on an island increases dramatically in comparison to its mainland relatives.
The pygmy mammoth is an example of insular dwarfism, a case of Foster's rule, its unusually small body size an adaptation to the limited resources of its island home.. A biological rule or biological law is a generalized law, principle, or rule of thumb formulated to describe patterns observed in living organisms.
[27] [28] In landscape ecology, patches can be classified into a binary patch-matrix model based on island biogeography theory where a focal habitat patch type (e.g. seagrasses) is surrounded by an inhospitable matrix (e.g. sand), or a patch-mosaic of interconnected patches, where the interactions of the parts influence the ecological function ...
Species–area relationships are often evaluated in conservation science in order to predict extinction rates in the case of habitat loss and habitat fragmentation. [8] Authors have classified the species–area relationship according to the type of habitats being sampled and the census design used.
The terminology of r/K-selection was coined by the ecologists Robert MacArthur and E. O. Wilson in 1967 [2] based on their work on island biogeography; [3] although the concept of the evolution of life history strategies has a longer history [4] (see e.g. plant strategies).