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Species richness

About: Species richness is a research topic. Over the lifetime, 61672 publications have been published within this topic receiving 2183796 citations.


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TL;DR: It is suggested that insular mammalian faunas typically are not in equilibrium, brrause geological and climatic changes can occur as rapidly as colonization and speciation, and any model of island biogeography to be widely applicable to insular faunaas must include speciation as a major variable.
Abstract: Four categories of islands in SE Asia may be identified on the basis of their histories of landbridge connections. Those islands on the shallow, continental Sunda Shelf were joined to the Asian mainland by a broad landbridge during the late Pleistocene; other islands were connected to the Sunda Shelf by a middle Pleistocene landbridge; some were parts of larger oceanic islands; and others remained as isolated oceanic islands. The limits of late Pleistocene islands, defined by the 120 ni bathymetric line, are highly concordant with the limits of faunal regions. Faunal variation among non-volant mammals is high between faunal regions and low within the faunal regions; endcmism of faunal regions characteristically exceeds 70%. Small and geologically young oceanic islands are depauperate; larger and older islands are more species-rich. The number of endemic species is correlated with island area; however, continental shelf islands less than 125000 km2 do not have endemic species, whereas isolated oceanic islands as small as 47 km2 often have endemic species. Geologirally old oceanic islands have many endemic species, whereas young oceanic islands have few endemic species. Colonization across sea channels that were 5-25 km wide during the Pleistocene has been low, with a rate of about 1-2/500000 years. Comparison ofspecies-area curves for mainland areas, late Pleistocene islands, and middle Pleistocene islands indicates that extinction occurs rapidly when landbridge islands are first isolated, with the extent of extinction dependent upon island size; extinction then slows to an average rate of 1-2"/0/10000 years. The great majority of the non-volant Philippine mammals arrived from the Sunda Shelf, the geographically closest of the possible source areas. Speciation within the Philippines has contributed substantially to species richness, perhaps exceeding colonization by a factor of two or more as a contributor to species number. Colonization, extinction and speciation rates differ among taxonomic groups, with murid rodents being most successful and carnivores least successful. In order for any model of island biogeography to be widely applicable to insular faunas, the model must include speciation as a major variable. It is suggested that insular mammalian faunas typically are not in equilibrium, brrause geological and climatic changes can occur as rapidly as colonization and speciation.

400 citations

Journal ArticleDOI
TL;DR: By analysing data sets from different world regions, evidence is added to documented changes in demersal fish community structure that may be related to fishing that the slope of size spectra appears to respond in a consistent way to changes in exploitation levels.
Abstract: By analysing data sets from different world regions we add evidence to documented changes in demersal fish community structure that may be related to fishing. Changes are analysed by community properties that might be expected to capture relevant overall changes – size spectra slopes and intercepts, Shannon-Wiener diversity, and dominance. Cross-system differences in the shape of the integrated community size spectra appear to be related to ecosystem productivity. The slope of size spectra appears to respond in a consistent way to changes in exploitation levels. In most areas studied, but particularly in high-latitude regions, we observe a decreasing trend in the slope, reflecting changes in size composition toward a relative decline in larger fish. The results from tropical regions are less conclusive, partly owing to the difficulty in obtaining consistent data series, but probably also because the generally higher growth rates of the constituent species make the slope less sensitive to changes in fishing. No evidence was found of any decline in species richness, while changes in diversity (richness and evenness) were caused either by changes in patterns of dominance or by changes in the number of species identified resulting from improved survey protocols.

400 citations

Journal ArticleDOI
TL;DR: This work uses data from the longest-running biodiversity-functioning field experiment to date to test how species diversity affects the ability of grassland ecosystems to provide threshold levels of up to eight ecosystem functions simultaneously.
Abstract: Society places value on the multiple functions of ecosystems from soil fertility to erosion control to wildlife-carrying capacity, and these functions are potentially threatened by ongoing biodiversity losses. Recent empirically based models using individual species’ traits suggest that higher species richness is required to provide multiple ecosystem functions. However, no study to date has analyzed the observed functionality of communities of interacting species over multiple temporal scales to assess the relationship between biodiversity and multifunctionality. We use data from the longest-running biodiversity-functioning field experiment to date to test how species diversity affects the ability of grassland ecosystems to provide threshold levels of up to eight ecosystem functions simultaneously. Across years and every combination of ecosystem functions, minimum-required species richness consistently increases with the number of functions considered. Moreover, tradeoffs between functions and variability among years prevent any one community type from providing high levels of multiple functions, regardless of its diversity. Sustained multifunctionality, therefore, likely requires both higher species richness than single ecosystem functionality and a diversity of species assemblages across the landscape.

399 citations

Journal ArticleDOI
03 Mar 2017-Science
TL;DR: Analysis of plant distributions, archaeological sites, and environmental data indicates that modern tree communities in Amazonia are structured to an important extent by a long history of plant domestication by Amazonian peoples.
Abstract: The extent to which pre-Columbian societies altered Amazonian landscapes is hotly debated. We performed a basin-wide analysis of pre-Columbian impacts on Amazonian forests by overlaying known archaeological sites in Amazonia with the distributions and abundances of 85 woody species domesticated by pre-Columbian peoples. Domesticated species are five times more likely than nondomesticated species to be hyperdominant. Across the basin, the relative abundance and richness of domesticated species increase in forests on and around archaeological sites. In southwestern and eastern Amazonia, distance to archaeological sites strongly influences the relative abundance and richness of domesticated species. Our analyses indicate that modern tree communities in Amazonia are structured to an important extent by a long history of plant domestication by Amazonian peoples.

398 citations

Journal ArticleDOI
TL;DR: Pielou’s evenness measure J is shown to be such a measure, which gives the amount of evenness relative to the maximum and minimum possible for a given richness.
Abstract: Contrary to common belief, decomposition of diversity into independent richness and evenness components is mathematically impossible. However, richness can be decomposed into independent diversity and evenness or inequality components. The evenness or inequality component derived in this way is connected to most of the common measures of evenness and inequality in ecology and economics. This perspective justifies the derivation of measures of relative evenness, which give the amount of evenness relative to the maximum and minimum possible for a given richness. Pielou’s [1] evenness measure J is shown to be such a measure.

398 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20243
20232,454
20225,118
20213,510
20203,287
20193,254