Biogeographic area relationships of lowland Neotropical rainforest based on raw distributions of vertebrate groups

By S. Ron. 2000

151 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Paleontology

View Paper: https://www.semanticscholar.org/paper/2ed961dded0647a0fd4df02f0fab97e3dd249717

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Global and Planetary Change

In Paleontology

Citations in the corpus

The combined influence of riverine barriers and flooding gradients on biogeographical patterns for amphibians and squamates in south‐eastern Amazonia (2016, background): “…a few studies have addressed variation in assemblage structure, and those that do exist show that both historical and ecological factors have helped shape species’ distributions within these groups at different scales ( AvilaPires, 1995; Gascon et al., 2000; Ron, 2000; Dias-Terceiro et al., 2015).”
Parsimony analysis of endemicity (PAE) of Mexican terrestrial mammals at different area units: when size matters (2002, background): “If the subset of information considered by PAE is large enough, area cladograms representing accurately the history of vicariant events should be expected and results should be similar to those derived from cladistic biogeographical analyses (Ron, 2000).”
Review of plant biogeographic studies in Brazil (2009, methodology): “Regardless of the methodology used, raw distributions or taxon phylogenies, relationships among Amazonian areas of endemism seem to show some degree of congruence (Ron, 2000; Hall & Harvey, 2002).”
Historical biogeography and diversification within the Neotropical parrot genus Pionopsitta (Aves: Psittacidae) (2005, methodology): “At the same time, some authors have attempted to reconstruct the history of the lowland biota using methods that do not rely explicitly on knowledge of phylogenetic relationships, and not unexpectedly these too have revealed similarities and differences in biogeographical pattern (e.g. Bates et al.,”
Cladistic analysis of distributions and endemism (CADE): using raw distributions of birds to unravel the biogeography of the South American aridlands (2005, methodology): “We did not treat other regions such as AMN or AMS in the same manner because others have already explored these areas in detail (Cracraft & Prum, 1988; Silva & Oren, 1996; Bates et al., 1998; Ron, 2000).”
Real vs. artefactual absences in species distributions: tests for Oryzomys albigularis (Rodentia: Muridae) in Venezuela (2003, background): “…management and public health (e.g. Udvardy, 1969; MacArthur, 1972; Nelson & Platnick, 1981; Brooks & McLennan, 1991; Ricklefs & Schluter, 1993; Mace & Stuart, 1994; Funk et al., 1999; Ron, 2000; Zalba et al., 2000; Peterson & Vieglais, 2001; Lizcano et al., 2002; Rodrigues-Coura et al., 2002).”
The Fate of the Amazonian Areas of Endemism (2005, background): “Recent studies support these areas of endemism (e.g., Ávila-Pires 1995, lizards; Silva & Oren 1996, primates; Ron 2000, frogs).”
Regionalization of the avifauna of the Baja California Peninsula, Mexico: a parsimony analysis of endemicity and distributional modelling approach (2003, background): “Many examples exist that show that PAE has been used to establish relationships among biogeographical units of diverse forms and sizes (Craw, 1989; Cracraft, 1991; Myers, 1991; Morrone, 1994; Fernandes et al., 1995, Morrone & Lopretto, 1995; Da Silva & Oren, 1996; Posadas, 1996; Bellan & Bellan-Sant”
Misconceptions about parsimony analysis of endemicity (2006, background): “These same authors argue that the ideal organisms for PAE analysis are those with limited dispersal abilities and for which speciation is vicariant (Ron, 2000; Morrone & Escalante, 2002).”
Biogeographical relationships among tropical forests in north‐eastern Brazil (2007, background): “However, cladistic methods require information about the phylogeny of taxa distributed allopatrically in the target regions and there are few well-supported phylogenetic hypotheses for most plants and animals inhabiting the Neotropical region (Ron, 2000).”
Areas of endemism of vascular plants in the Eastern Alps in relation to Pleistocene glaciation (2004, methodology): “In particular, Parsimony Analysis of Endemicity (PAE) is regarded as a suitable method to detect AOEs, under the assumption that distributional patterns are mainly caused by vicariance, and dispersal and extinction are limited (Ron, 2000; Linder, 2001b; Morrone & Escalante, 2002).”
Historical biogeography of South American freshwater fishes (2006, background): “2) based on distributional data among birds (Cracraft, 1985; Prum, 1988), butterflies (Hall & Harvey, 2002; Racheli & Racheli, 2004), anurans and lizards (Ron, 2000), and were further confirmed by several molecular phylogenetic studies (Aleixo,”
Biogeographic areas and transition zones of Latin America and the Caribbean islands based on panbiogeographic and cladistic analyses of the entomofauna. (2006, background): “Several PAE and cladistic biogeographic analyses have reconstructed the relationships among Amazonian provinces (2, 17, 45, 114, 122, 139, 155), but there is little agreement among the alternative hypotheses.”
Areas of endemism for passerine birds in the Atlantic forest, South America (2004, methodology): “90 Global Ecology and Biogeography , 13 , 85–92, © 2004 Blackwell Publishing Ltd from this method are congruent with those obtained using more sophisticated biogeographical analyses based on cladistic biogeography methods and on the phylogenies of different groups of species (e.g. Cracraft, 1991, 19”
Parsimony analysis of endemicity (PAE) revisited (2014, methodology): “Some authors, however, have explored partitioning the data matrix into separate sets (e.g. Cracraft, 1991; Myers, 1991; Morrone, 1998; Ron, 2000; Garc ıa-Trejo & Navarro, 2004; Porzecanski & Cracraft, 2005; Fattorini, 2009a,b; Watanabe, 2012).”