The species–area relationship or species–area curve describes the relationship between the area of a habitat, or of part of a habitat, and the number of species found within that area. Larger areas tend to contain larger numbers of species, and empirically, the relative numbers seem to follow systematic mathematical relationships. The species–area relationship is usually constructed for a single type of organism, such as all vascular plants or all species of a specific trophic level within a particular site. It is rarely if ever, constructed for all types of organisms if simply because of the prodigious data requirements. It is related but not identical to the species discovery curve.
Ecologists have proposed a wide range of factors determining the slope and elevation of the species–area relationship. These factors include the relative balance between immigration and extinction, rate and magnitude of disturbance on small vs. large areas, predator-prey dynamics, and clustering of individuals of the same species as a result of dispersal limitation or habitat heterogeneity. The species–area relationship has been reputed to follow from the 2nd law of thermodynamics. In contrast to these "mechanistic" explanations, others assert the need to test whether the pattern is simply the result of a random sampling process. Species–area relationships are often evaluated in conservation science in order to predict extinction rates in the case of habitat loss and habitat fragmentation.
Authors have classified the species–area relationship according to the type of habitats being sampled and the census design used. Frank W. Preston, an early investigator of the theory of the species–area relationship, divided it into two types: samples (a census of a contiguous habitat that grows in the census area, also called "mainland" species–area relationships), and isolates (a census of discontiguous habitats, such as islands, also called "island" species–area relationships).
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