What’s in a name?: Mesoamerica

Definition of biogeographic regions, the primary objective of biogeographic regionalization (Escalante, 2009), has been under considerable debate, as the limits between some of them are often poorly defined as a consequence of geological and/or biotic complexities (Cox, 2001; Morrone, 2002; Riddle a...

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Autores:
Tipo de recurso:
Article of journal
Fecha de publicación:
2013
Institución:
Universidad de Bogotá Jorge Tadeo Lozano
Repositorio:
Expeditio: repositorio UTadeo
Idioma:
spa
OAI Identifier:
oai:expeditiorepositorio.utadeo.edu.co:20.500.12010/13653
Acceso en línea:
https://www.elsevier.es/es-revista-revista-mexicana-biodiversidad-91-articulo-what39s-in-name-mesoamerica-S1870345313729609
http://hdl.handle.net/20.500.12010/13653
Palabra clave:
Biogeographic regions
Geological
Neotropical regions
History
Rights
License
Abierto (Texto Completo)
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dc.title.spa.fl_str_mv What’s in a name?: Mesoamerica
dc.title.alternative.spa.fl_str_mv ¿Qué hay en un nombre?: Mesoamérica
title What’s in a name?: Mesoamerica
spellingShingle What’s in a name?: Mesoamerica
Biogeographic regions
Geological
Neotropical regions
History
title_short What’s in a name?: Mesoamerica
title_full What’s in a name?: Mesoamerica
title_fullStr What’s in a name?: Mesoamerica
title_full_unstemmed What’s in a name?: Mesoamerica
title_sort What’s in a name?: Mesoamerica
dc.subject.spa.fl_str_mv Biogeographic regions
Geological
Neotropical regions
History
topic Biogeographic regions
Geological
Neotropical regions
History
description Definition of biogeographic regions, the primary objective of biogeographic regionalization (Escalante, 2009), has been under considerable debate, as the limits between some of them are often poorly defined as a consequence of geological and/or biotic complexities (Cox, 2001; Morrone, 2002; Riddle and Hafner, 2010). These limits may coincide with transitional complex regions –like the Mexican Transition Zone (Halftter, 1976; Savage, 1960, 1966; Morrone, 2010)– which show mixed biotic elements from 2 different biogeographic regions (the Nearctic and Neotropical regions). The admixture of biotic elements in such transition zones implies that delimitation of biogeographic regions is not an easy task, as the history of biogeography has shown (e.g., Townsend, 1895; Halffter, 1976; Ortega and Arita, 1998). In an attempt to describe a system that would “reflect the origination and development of distinctive avian biotas”, P. L. Sclater proposed a scheme dividing the Earth into biogeographic regions (Brown and Lomolino, 2000). Sclater acknowledged that different biogeographic schemes had been proposed before him; however, these were based mainly on non-natural properties, such as latitude or longitude (Sclater, 1858). Sclater's scheme was greatly improved by Wallace (1876), who analyzed the geographical distribution of different vertebrate taxa, focusing on organismic attributes such as their dispersal abilities. Although Wallace's biogeographic scheme included sharp divisions between regions and subregions, he was the first author to propose natural boundaries for regions by using a bathymetric scale for description of isolation in archipelagos, as in Southeast Asia (Brown and Lomolino, 2000). Clearly, attempts by Sclater (1858), Wallace (1876), and other authors to delimit biogeographic regions were directed at understanding biotic evolutionary patterns on ecological and environmental bases, not at defining arbitrary boundaries, as was recognized by Udvardy (1975). In this sense, the recognition of biogeographic regions on the basis of politically defined boundaries is not useful, as they are not ecologically or evolutionary meaningful.
publishDate 2013
dc.date.created.none.fl_str_mv 2013
dc.date.accessioned.none.fl_str_mv 2020-09-23T01:59:10Z
dc.date.available.none.fl_str_mv 2020-09-23T01:59:10Z
dc.type.local.spa.fl_str_mv Artículo
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_6501
format http://purl.org/coar/resource_type/c_6501
dc.identifier.other.none.fl_str_mv https://www.elsevier.es/es-revista-revista-mexicana-biodiversidad-91-articulo-what39s-in-name-mesoamerica-S1870345313729609
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12010/13653
dc.identifier.doi.none.fl_str_mv DOI: 10.7550/rmb.34171
url https://www.elsevier.es/es-revista-revista-mexicana-biodiversidad-91-articulo-what39s-in-name-mesoamerica-S1870345313729609
http://hdl.handle.net/20.500.12010/13653
identifier_str_mv DOI: 10.7550/rmb.34171
dc.language.iso.spa.fl_str_mv spa
language spa
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dc.rights.local.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
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dc.format.extent.spa.fl_str_mv 4 páginas
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dc.publisher.spa.fl_str_mv Revista Mexicana de Biodiversidad
dc.source.none.fl_str_mv instname:Universidad Jorge Tadeo Lozano
reponame:Repositorio Institucional UJTL
instname_str Universidad Jorge Tadeo Lozano
institution Universidad de Bogotá Jorge Tadeo Lozano
reponame_str Repositorio Institucional UJTL
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spelling 2020-09-23T01:59:10Z2020-09-23T01:59:10Z2013https://www.elsevier.es/es-revista-revista-mexicana-biodiversidad-91-articulo-what39s-in-name-mesoamerica-S1870345313729609http://hdl.handle.net/20.500.12010/13653DOI: 10.7550/rmb.34171Definition of biogeographic regions, the primary objective of biogeographic regionalization (Escalante, 2009), has been under considerable debate, as the limits between some of them are often poorly defined as a consequence of geological and/or biotic complexities (Cox, 2001; Morrone, 2002; Riddle and Hafner, 2010). These limits may coincide with transitional complex regions –like the Mexican Transition Zone (Halftter, 1976; Savage, 1960, 1966; Morrone, 2010)– which show mixed biotic elements from 2 different biogeographic regions (the Nearctic and Neotropical regions). The admixture of biotic elements in such transition zones implies that delimitation of biogeographic regions is not an easy task, as the history of biogeography has shown (e.g., Townsend, 1895; Halffter, 1976; Ortega and Arita, 1998). In an attempt to describe a system that would “reflect the origination and development of distinctive avian biotas”, P. L. Sclater proposed a scheme dividing the Earth into biogeographic regions (Brown and Lomolino, 2000). Sclater acknowledged that different biogeographic schemes had been proposed before him; however, these were based mainly on non-natural properties, such as latitude or longitude (Sclater, 1858). Sclater's scheme was greatly improved by Wallace (1876), who analyzed the geographical distribution of different vertebrate taxa, focusing on organismic attributes such as their dispersal abilities. Although Wallace's biogeographic scheme included sharp divisions between regions and subregions, he was the first author to propose natural boundaries for regions by using a bathymetric scale for description of isolation in archipelagos, as in Southeast Asia (Brown and Lomolino, 2000). Clearly, attempts by Sclater (1858), Wallace (1876), and other authors to delimit biogeographic regions were directed at understanding biotic evolutionary patterns on ecological and environmental bases, not at defining arbitrary boundaries, as was recognized by Udvardy (1975). 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