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      Accurate and precise estimates of origination and extinction rates

      Paleobiology
      Paleontological Society

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          Abstract

          Paleobiologists have used many different methods for estimating rates of origination and extinction. Unfortunately, all equations that consider entire age ranges are distorted by the Pull of the Recent, the Signor-Lipps effect, and simple edge effects. Attention has been paid recently to an equation of Foote's that considers counts of taxa either crossing the bottom and top of an interval or crossing one boundary but not the other. This generalized boundary-crosser (BC) method has important advantages but is still potentially subject to the major biases. The only published equation that circumvents all of them is the three-timer (3T) log ratio, which does so by focusing on a four-interval moving window. Although it is highly accurate it is noisy when turnover rates are very high or sampling is very poor. More precise values are yielded by a newly derived equation that uses the same counts. However, it also considers taxa sampled in a window's first and fourth intervals but missing from the third (i.e., gap-fillers). Simulations show that the 3T, gap-filler (GF), and BC equations yield identical values when sampling and turnover are uniform through time. When applied to Phanerozoic-scale marine animal data, 3T and GF agree well but the BC rates are systematically lower. The apparent reason is that (1) long-ranging but infrequently sampled genera are less likely to be split up by taxonomists and (2) the BC equation overweights taxa with long ranges. Thus, BC rates pertain more to rare genera that are likely to represent large clades whereas GF rates pertain more to actual species-level patterns. Given these results, all published turnover rates based either on genus-level data or on age ranges must be reconsidered because they may reflect taxonomic practices more strongly than the species-level dynamics of interest to biologists.

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          The operated Markov´s chains in economy (discrete chains of Markov with the income)

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            Mass extinctions in the marine fossil record.

            A new compilation of fossil data on invertebrate and vertebrate families indicates that four mass extinctions in the marine realm are statistically distinct from background extinction levels. These four occurred late in the Ordovician, Permian, Triassic, and Cretaceous periods. A fifth extinction event in the Devonian stands out from the background but is not statistically significant in these data. Background extinction rates appear to have declined since Cambrian time, which is consistent with the prediction that optimization of fitness should increase through evolutionary time.
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              EXTINCTION VULNERABILITY AND SELECTIVITY:Combining Ecological and Paleontological Views

              Extinction is rarely random across ecological and geological time scales. Traits that make some species more extinction-prone include individual traits, such as body size, and abundance. Substantial consistency appears across ecological and geological time scales in such traits. Evolutionary branching produces phylogenetic (as often measured by taxonomic) nesting of extinction-biasing traits at many scales. An example is the tendency, seen in both fossil and modern data, for higher taxa living in marine habitats to have generally lower species extinction rates. At lower taxononomic levels, recent bird and mammal extinctions are concentrated in certain genera and families. A fundamental result of such selectivity is that it can accelerate net loss of biodiversity compared to random loss of species among taxa. Replacement of vulnerable taxa by rapidly spreading taxa that thrive in human-altered environments will ultimately produce a spatially more homogenized biosphere with much lower net diversity.
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                Author and article information

                Journal
                Paleobiology
                Paleobiology
                Paleontological Society
                0094-8373
                1938-5331
                2014
                April 08 2016
                2014
                : 40
                : 3
                : 374-397
                Article
                10.1666/13036
                bdfb5ceb-6071-4238-8d26-9332177d2a16
                © 2014

                https://www.cambridge.org/core/terms

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