Climate niche shift in invasive species: the case of the brown anole
Identifieur interne : 001A22 ( Istex/Corpus ); précédent : 001A21; suivant : 001A23Climate niche shift in invasive species: the case of the brown anole
Auteurs : Lea-Su Angetter ; Stefan Lötters ; Dennis RödderSource :
- Biological Journal of the Linnean Society [ 0024-4066 ] ; 2011-12.
English descriptors
- KwdEn :
Abstract
Anolis sagrei, a Cuba and Bahama native lizard, is a successful invader in Florida and adjacent areas. Herein, we focus on conservatism in its climate niche axes and possible congruencies with its natural history properties. The not mutually exclusive hypotheses of the present study explaining its northern range limit are: (1) climatic conditions within species' native and invasive ranges are identical; (2) the species is pre‐adapted to novel conditions as a result of historical climate variations; and (3) only some niche axes limit the species' invasive distribution and the observed pattern is explained by an interplay between the potential niche within its native range and life‐history. Species distribution models for native and invasive distributions were built on ten bioclimatic variables. Using Schoener's niche overlap index, the degree of niche conservatism among variables was identified. Significances of hypothesis (1) were tested using null‐model approaches. Possible climatic pre‐adaptations were evaluated by comparing its actual tolerance within its invasive range with that of the Last Glacial Maximum (LGM) within its native range (hypothesis 2). Results of (1) and (2) are discussed in relation to natural history, approaching hypothesis 3. We detect varying overlaps in niche axes, indicating that natural history properties are associated with conservative niche axes. Climatic comparisons with LGM of native and current conditions of invasive range suggest that pre‐adaptations are unlikely. Possible shifts in the fundamental niche of the species may have been facilitated by enhanced genetic diversity in northern invasive populations. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 104, 943–954.
Url:
DOI: 10.1111/j.1095-8312.2011.01780.x
Links to Exploration step
ISTEX:44EFAAE005DC9F955A066BE4BE5B360C1AE08749Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Climate niche shift in invasive species: the case of the brown anole</title><author><name sortKey="Angetter, Lea U" sort="Angetter, Lea U" uniqKey="Angetter L" first="Lea-Su" last="Angetter">Lea-Su Angetter</name><affiliation><mods:affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Lotters, Stefan" sort="Lotters, Stefan" uniqKey="Lotters S" first="Stefan" last="Lötters">Stefan Lötters</name><affiliation><mods:affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Rodder, Dennis" sort="Rodder, Dennis" uniqKey="Rodder D" first="Dennis" last="Rödder">Dennis Rödder</name><affiliation><mods:affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: d.roedder.zfmk@uni‐bonn.de</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:44EFAAE005DC9F955A066BE4BE5B360C1AE08749</idno><date when="2011" year="2011">2011</date><idno type="doi">10.1111/j.1095-8312.2011.01780.x</idno><idno type="url">https://api.istex.fr/document/44EFAAE005DC9F955A066BE4BE5B360C1AE08749/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">001A22</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001A22</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Climate niche shift in invasive species: the case of the brown anole</title><author><name sortKey="Angetter, Lea U" sort="Angetter, Lea U" uniqKey="Angetter L" first="Lea-Su" last="Angetter">Lea-Su Angetter</name><affiliation><mods:affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Lotters, Stefan" sort="Lotters, Stefan" uniqKey="Lotters S" first="Stefan" last="Lötters">Stefan Lötters</name><affiliation><mods:affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</mods:affiliation></affiliation></author><author><name sortKey="Rodder, Dennis" sort="Rodder, Dennis" uniqKey="Rodder D" first="Dennis" last="Rödder">Dennis Rödder</name><affiliation><mods:affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: d.roedder.zfmk@uni‐bonn.de</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Biological Journal of the Linnean Society</title><idno type="ISSN">0024-4066</idno><idno type="eISSN">1095-8312</idno><imprint><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2011-12">2011-12</date><biblScope unit="volume">104</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="943">943</biblScope><biblScope unit="page" to="954">954</biblScope></imprint><idno type="ISSN">0024-4066</idno></series><idno type="istex">44EFAAE005DC9F955A066BE4BE5B360C1AE08749</idno><idno type="DOI">10.1111/j.1095-8312.2011.01780.x</idno><idno type="ArticleID">BIJ1780</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0024-4066</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anolis sagrei</term><term>bioclimatic variables</term><term>historical climate variation</term><term>last glacial maximum</term><term>maxent</term><term>species distribution model</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract">Anolis sagrei, a Cuba and Bahama native lizard, is a successful invader in Florida and adjacent areas. Herein, we focus on conservatism in its climate niche axes and possible congruencies with its natural history properties. The not mutually exclusive hypotheses of the present study explaining its northern range limit are: (1) climatic conditions within species' native and invasive ranges are identical; (2) the species is pre‐adapted to novel conditions as a result of historical climate variations; and (3) only some niche axes limit the species' invasive distribution and the observed pattern is explained by an interplay between the potential niche within its native range and life‐history. Species distribution models for native and invasive distributions were built on ten bioclimatic variables. Using Schoener's niche overlap index, the degree of niche conservatism among variables was identified. Significances of hypothesis (1) were tested using null‐model approaches. Possible climatic pre‐adaptations were evaluated by comparing its actual tolerance within its invasive range with that of the Last Glacial Maximum (LGM) within its native range (hypothesis 2). Results of (1) and (2) are discussed in relation to natural history, approaching hypothesis 3. We detect varying overlaps in niche axes, indicating that natural history properties are associated with conservative niche axes. Climatic comparisons with LGM of native and current conditions of invasive range suggest that pre‐adaptations are unlikely. Possible shifts in the fundamental niche of the species may have been facilitated by enhanced genetic diversity in northern invasive populations. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 104, 943–954.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>LEA‐SU ANGETTER</name><affiliations><json:string>Department of Biogeography, Trier University, 54286 Trier, Germany</json:string></affiliations></json:item><json:item><name>STEFAN LÖTTERS</name><affiliations><json:string>Department of Biogeography, Trier University, 54286 Trier, Germany</json:string></affiliations></json:item><json:item><name>DENNIS RÖDDER</name><affiliations><json:string>Department of Biogeography, Trier University, 54286 Trier, Germany</json:string><json:string>Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany</json:string><json:string>E-mail: d.roedder.zfmk@uni‐bonn.de</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Anolis sagrei</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bioclimatic variables</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>historical climate variation</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>last glacial maximum</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>maxent</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>species distribution model</value></json:item></subject><articleId><json:string>BIJ1780</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Anolis sagrei, a Cuba and Bahama native lizard, is a successful invader in Florida and adjacent areas. Herein, we focus on conservatism in its climate niche axes and possible congruencies with its natural history properties. The not mutually exclusive hypotheses of the present study explaining its northern range limit are: (1) climatic conditions within species' native and invasive ranges are identical; (2) the species is pre‐adapted to novel conditions as a result of historical climate variations; and (3) only some niche axes limit the species' invasive distribution and the observed pattern is explained by an interplay between the potential niche within its native range and life‐history. Species distribution models for native and invasive distributions were built on ten bioclimatic variables. Using Schoener's niche overlap index, the degree of niche conservatism among variables was identified. Significances of hypothesis (1) were tested using null‐model approaches. Possible climatic pre‐adaptations were evaluated by comparing its actual tolerance within its invasive range with that of the Last Glacial Maximum (LGM) within its native range (hypothesis 2). Results of (1) and (2) are discussed in relation to natural history, approaching hypothesis 3. We detect varying overlaps in niche axes, indicating that natural history properties are associated with conservative niche axes. Climatic comparisons with LGM of native and current conditions of invasive range suggest that pre‐adaptations are unlikely. Possible shifts in the fundamental niche of the species may have been facilitated by enhanced genetic diversity in northern invasive populations. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 104, 943–954.</abstract><qualityIndicators><score>8</score><pdfVersion>1.3</pdfVersion><pdfPageSize>595.276 x 782.362 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>1769</abstractCharCount><pdfWordCount>7826</pdfWordCount><pdfCharCount>51314</pdfCharCount><pdfPageCount>12</pdfPageCount><abstractWordCount>257</abstractWordCount></qualityIndicators><title>Climate niche shift in invasive species: the case of the brown anole</title><refBibs><json:item><author><json:item><name>JM Alexander</name></json:item><json:item><name>PJ Edwards</name></json:item></author><host><volume>119</volume><pages><last>1386</last><first>1377</first></pages><author></author><title>Oikos</title></host><title>Limits to the niche and range margins of alien species</title></json:item><json:item><author><json:item><name>RP Anderson</name></json:item><json:item><name>A Raza</name></json:item></author><host><volume>37</volume><pages><last>1393</last><first>1378</first></pages><author></author><title>Journal of Biogeography</title></host><title>The effect of the extend of the study region on GIS models of species geographic distributions and estimates of niche evolution: preliminary tests with montane rodents (genus Nephelomys) in Venezuela</title></json:item><json:item><author><json:item><name>R Andrews</name></json:item><json:item><name>OJ Sexton</name></json:item></author><host><volume>62</volume><pages><last>562</last><first>556</first></pages><author></author><title>Ecology</title></host><title>Water relations of the eggs of Anolis auratus and Anolis limifrons</title></json:item><json:item><author><json:item><name>MB Araújo</name></json:item><json:item><name>M Cabeza</name></json:item><json:item><name>W Thullier</name></json:item><json:item><name>L Hannah</name></json:item><json:item><name>PH Williams</name></json:item></author><host><volume>10</volume><pages><last>1626</last><first>1618</first></pages><author></author><title>Global Change Biology</title></host><title>Would climate change drive species out of reserves? An assessment of existing reserve‐selection methods</title></json:item><json:item><author><json:item><name>MB Araújo</name></json:item><json:item><name>RG Pearson</name></json:item></author><host><volume>28</volume><pages><last>695</last><first>693</first></pages><author></author><title>Ecography</title></host><title>Equilibrium of species' distributions with climate</title></json:item><json:item><author><json:item><name>MB Araújo</name></json:item><json:item><name>W Thuiller</name></json:item><json:item><name>RG Pearson</name></json:item></author><host><volume>33</volume><pages><last>1728</last><first>1712</first></pages><author></author><title>Journal of Biogeography</title></host><title>Climate warming and the decline of amphibians and reptiles in Europe</title></json:item><json:item><author><json:item><name>LJ Beaumont</name></json:item><json:item><name>L Hughes</name></json:item><json:item><name>M Poulsen</name></json:item></author><host><volume>186</volume><pages><last>269</last><first>250</first></pages><author></author><title>Ecological Modelling</title></host><title>Predicting species distributions: use of climatic parameters in bioclim and its impact on predictions of species' current and future distributions</title></json:item><json:item><author><json:item><name>M Bomford</name></json:item><json:item><name>F Kraus</name></json:item><json:item><name>SC Barry</name></json:item><json:item><name>E Lawrence</name></json:item></author><host><volume>11</volume><pages><last>3547</last><first>1387</first></pages><author></author><title>Biological Invasions</title></host><title>Predicting establishment success for alien reptiles and amphibians: a role for climate matching</title></json:item><json:item><author><json:item><name>O Broennimann</name></json:item><json:item><name>UA Treier</name></json:item><json:item><name>H Müller‐Schärer</name></json:item><json:item><name>W Thuiller</name></json:item><json:item><name>AT Peterson</name></json:item><json:item><name>A Guisan</name></json:item></author><host><volume>10</volume><pages><last>709</last><first>701</first></pages><author></author><title>Ecology Letters</title></host><title>Evidence of climatic nich shift during biological invasion</title></json:item><json:item><author><json:item><name>JJ Bull</name></json:item></author><host><volume>55</volume><pages><last>21</last><first>3</first></pages><author></author><title>Quaterly Review of Biology</title></host><title>Sex determination in reptiles</title></json:item><json:item><author><json:item><name>JR Busby</name></json:item></author><host><pages><last>68</last><first>64</first></pages><author></author><title>Nature conservation: cost effective biological surveys and data analysis</title></host><title>Bioclim – a bioclimatic analysis and prediction system</title></json:item><json:item><author><json:item><name>TS Campbell</name></json:item></author><host><volume>27</volume><pages><last>157</last><first>155</first></pages><author></author><title>Herpetological Review</title></host><title>Northern range expansion of the brown anole (Anolis sagrei) in Florida and Georgia</title></json:item><json:item><author><json:item><name>TS Campbell</name></json:item></author><host><volume>V</volume><pages><last>21</last><first>12</first></pages><author></author><title>Anolis Newsletter</title></host><title>Consequences of the Cuban brown anole invasion: it's not easy being green</title></json:item><json:item><host><author></author><title>Analyses of the effects of an exotic lizard (Anolis sagrei) on a native lizard (Anolis carolinensis) in Florida, using islands as experimental units</title></host></json:item><json:item><author><json:item><name>TS Campbell</name></json:item></author><host><volume>10</volume><pages><last>5</last><first>4</first></pages><author></author><title>Aliens Newsletter</title></host><title>The Cuban brown anole invasion in Florida: it's not easy to be green</title></json:item><json:item><author><json:item><name>TS Campbell</name></json:item><json:item><name>AC Echternacht</name></json:item></author><host><volume>5</volume><pages><last>212</last><first>193</first></pages><author></author><title>Biological Invasions</title></host><title>Introduced species as moving targets: changes in body sizes of introduced lizards following experimental introductions and historical invasions</title></json:item><json:item><author><json:item><name>TS Campbell</name></json:item><json:item><name>GP Gerber</name></json:item></author><host><volume>27</volume><pages><first>106</first></pages><author></author><title>Herpetology Review</title></host><title>Natural history. Anolis sagrei. Saurophagy</title></json:item><json:item><author><json:item><name>TS Campbell</name></json:item><json:item><name>JT Hammontree</name></json:item></author><host><volume>26</volume><pages><first>107</first></pages><author></author><title>Herpetological Review</title></host><title>Anolis sagrei (brown anole)</title></json:item><json:item><author><json:item><name>DR Clark</name></json:item><json:item><name>JC Kroll</name></json:item></author><host><volume>18</volume><pages><last>19</last><first>9</first></pages><author></author><title>Southwestern Naturalist</title></host><title>Thermal ecology of anoline lizards: temperate versus tropical strategies</title></json:item><json:item><author><json:item><name>PA Cochran</name></json:item></author><host><volume>21</volume><pages><first>22</first></pages><author></author><title>Herpetological Review</title></host><title>Anolis sagrei. Geographic distribution note</title></json:item><json:item><author><json:item><name>NC Cole</name></json:item><json:item><name>CG Jones</name></json:item><json:item><name>S Harris</name></json:item></author><host><volume>125</volume><pages><last>474</last><first>467</first></pages><author></author><title>Biological Conservation</title></host><title>The need for enemy‐free space; the impact of an invasive gecko on island endemics</title></json:item><json:item><author><json:item><name>MJ Corn</name></json:item></author><host><volume>5</volume><pages><last>21</last><first>17</first></pages><author></author><title>Journal of Herpetology</title></host><title>Upper thermal limits and thermal preferences for three sympatric species of Anolis</title></json:item><json:item><author><json:item><name>CF Dormann</name></json:item><json:item><name>J Mcpherson</name></json:item><json:item><name>MB Araújo</name></json:item><json:item><name>R Bivand</name></json:item><json:item><name>J Bollinger</name></json:item><json:item><name>G Carl</name></json:item><json:item><name>RG Davies</name></json:item><json:item><name>A Hirzel</name></json:item><json:item><name>W Jetz</name></json:item><json:item><name>WD Kissling</name></json:item><json:item><name>I Kühn</name></json:item><json:item><name>R Ohlemüller</name></json:item><json:item><name>PR Peres‐Neto</name></json:item><json:item><name>B Reineking</name></json:item><json:item><name>B Schröder</name></json:item><json:item><name>FM Schurr</name></json:item><json:item><name>R Wilson</name></json:item></author><host><volume>30</volume><pages><last>628</last><first>609</first></pages><author></author><title>Ecography</title></host><title>Methods to account for spatial autocorrelation in the analysis of species distributional data: a review</title></json:item><json:item><author><json:item><name>AC Echternacht</name></json:item></author><host><volume>V</volume><pages><last>27</last><first>22</first></pages><author></author><title>Anolis Newsletter</title></host><title>Possible causes for the rapid decline in population density of green anoles following invasion by the brown anole in the southeastern United States</title></json:item><json:item><author><json:item><name>J Elith</name></json:item><json:item><name>CH Graham</name></json:item><json:item><name>RP Anderson</name></json:item><json:item><name>M Dudik</name></json:item><json:item><name>S Ferrier</name></json:item><json:item><name>A Guisan</name></json:item><json:item><name>RJ Hijmans</name></json:item><json:item><name>F Huettmann</name></json:item><json:item><name>JR Leathwick</name></json:item><json:item><name>A Lehmann</name></json:item><json:item><name>J Li</name></json:item><json:item><name>LG Lohmann</name></json:item><json:item><name>BA Loiselle</name></json:item><json:item><name>G Manion</name></json:item><json:item><name>C Moritz</name></json:item><json:item><name>M Nakamura</name></json:item><json:item><name>Y Nakazawa</name></json:item><json:item><name>JMM Overton</name></json:item><json:item><name>AT Perterson</name></json:item><json:item><name>SJ Phillips</name></json:item><json:item><name>K Richardson</name></json:item><json:item><name>R Scachetti‐Pereira</name></json:item><json:item><name>RE Shapire</name></json:item><json:item><name>J Soberón</name></json:item><json:item><name>S Williams</name></json:item><json:item><name>MS Wisz</name></json:item><json:item><name>NE Zimmermann</name></json:item></author><host><volume>29</volume><pages><last>151</last><first>129</first></pages><author></author><title>Ecography</title></host><title>Novel methods improve prediction of species' distributions from occurrence data</title></json:item><json:item><author><json:item><name>J Elith</name></json:item><json:item><name>M Kearney</name></json:item><json:item><name>S Phillips</name></json:item></author><host><volume>1</volume><pages><last>342</last><first>330</first></pages><author></author><title>Methods in Ecology and Evolution</title></host><title>The art of modelling range‐shifting species</title></json:item><json:item><author><json:item><name>ME Evans</name></json:item><json:item><name>SA Smith</name></json:item><json:item><name>RS Flynn</name></json:item><json:item><name>MJ Donoghue</name></json:item></author><host><volume>173</volume><pages><last>240</last><first>225</first></pages><author></author><title>American Naturalist</title></host><title>Climate, niche evolution, diversification of the ‘bird‐cage’ evening primroses (Oenothera, sections Anogra and Kleinia)</title></json:item><json:item><author><json:item><name>MC Fitzpatrick</name></json:item><json:item><name>JF Weltzin</name></json:item><json:item><name>NJ Sanders</name></json:item><json:item><name>RR Dunn</name></json:item></author><host><volume>16</volume><pages><last>33</last><first>24</first></pages><author></author><title>Global Ecology and Biogeography</title></host><title>The biogeography of prediction error: why does the introduced range of the fire ant over‐predict its native range?</title></json:item><json:item><host><author></author><title>Free and open access to biodiversity data</title></host></json:item><json:item><author><json:item><name>GP Gerber</name></json:item></author><host><volume>V</volume><pages><last>39</last><first>28</first></pages><author></author><title>Anolis Newsletter</title></host><title>A review of intraguild predation and cannibalism in Anolis</title></json:item><json:item><author><json:item><name>GP Gerber</name></json:item><json:item><name>AC Echternacht</name></json:item></author><host><volume>124</volume><pages><last>607</last><first>599</first></pages><author></author><title>Oecologia</title></host><title>Evidence for asymmetrical intraguild predation between native and introduced Anolis lizards</title></json:item><json:item><author><json:item><name>SR Goldberg</name></json:item><json:item><name>F Kraus</name></json:item><json:item><name>CR Bursey</name></json:item></author><host><volume>56</volume><pages><last>168</last><first>163</first></pages><author></author><title>Pacific Science</title></host><title>Reproduction in an introduced population of brown anole, Anolis sagrei, from O'ahu, Hawaii</title></json:item><json:item><author><json:item><name>BT Green</name></json:item><json:item><name>DT Yorks</name></json:item><json:item><name>JS Parmerlee</name></json:item><json:item><name>R Powell</name></json:item><json:item><name>RW Henderson</name></json:item></author><host><volume>38</volume><pages><last>272</last><first>270</first></pages><author></author><title>Caribbean Journal of Science</title></host><title>Discovery of Anolis sagrei in Grenada with comments on its potential impact on native anoles</title></json:item><json:item><author><json:item><name>A Guisan</name></json:item><json:item><name>N Zimmermann</name></json:item></author><host><volume>135</volume><pages><last>186</last><first>147</first></pages><author></author><title>Ecological Modelling</title></host><title>Predictive habitat distribution models in ecology</title></json:item><json:item><host><author></author><title>K‐1 Coupled GCM (MIROC) description</title></host></json:item><json:item><author><json:item><name>RK Heikkinen</name></json:item><json:item><name>M Luoto</name></json:item><json:item><name>MB Araújo</name></json:item><json:item><name>R Virkkala</name></json:item><json:item><name>W Thuiller</name></json:item><json:item><name>MT Sykes</name></json:item></author><host><volume>30</volume><pages><last>777</last><first>751</first></pages><author></author><title>Progress in Physical Geography</title></host><title>Methods and uncertainities in bioclimatic envelope modelling under climate change</title></json:item><json:item><author><json:item><name>RW Henderson</name></json:item><json:item><name>MJ Powell</name></json:item></author><host><volume>36</volume><pages><first>467</first></pages><author></author><title>Herpetological Review</title></host><title>Geographic distribution: A. sagrei</title></json:item><json:item><host><author></author><title>Diva‐GIS version 5.2 manual</title></host></json:item><json:item><author><json:item><name>RJ Hijmans</name></json:item><json:item><name>SE Cameron</name></json:item><json:item><name>JL Parra</name></json:item><json:item><name>PG Jones</name></json:item><json:item><name>A Jarvis</name></json:item></author><host><volume>25</volume><pages><last>1978</last><first>1965</first></pages><author></author><title>International Journal of Climatology</title></host><title>Very high resolution interpolated climate surfaces for global land areas</title></json:item><json:item><author><json:item><name>RD Holt</name></json:item><json:item><name>M Barfield</name></json:item><json:item><name>R Gomulkiewicz</name></json:item></author><host><pages><last>290</last><first>259</first></pages><author></author><title>Species invasions: insight into ecology, evolution, and biogeography</title></host><title>Theories of niche conservatism and evolution: could exotic species be potential tests?</title></json:item><json:item><author><json:item><name>RB Huey</name></json:item><json:item><name>CA Deutsch</name></json:item><json:item><name>JJ Tewksbury</name></json:item><json:item><name>LJ Vitt</name></json:item><json:item><name>PE Hertz</name></json:item><json:item><name>HJ Alvarez Perez</name></json:item><json:item><name>T Garland Jr</name></json:item></author><host><volume>276</volume><pages><last>1948</last><first>1939</first></pages><author></author><title>Proceedings of the Royal Society of London Series B, Biological Sciences</title></host><title>Why tropical forest lizards are vulnerable to climate warming</title></json:item><json:item><author><json:item><name>GE Hutchinson</name></json:item></author><host><volume>22</volume><pages><last>427</last><first>415</first></pages><author></author><title>Cold Spring Harbor Symposia on Qantitative Biology</title></host><title>Concluding remarks</title></json:item><json:item><author><json:item><name>DR Jackson</name></json:item></author><host><volume>38</volume><pages><last>482</last><first>481</first></pages><author></author><title>Herpetological Review</title></host><title>Geographic distribution: Anolis sagrei</title></json:item><json:item><author><json:item><name>ST Jackson</name></json:item><json:item><name>JT Overpeck</name></json:item></author><host><volume>26</volume><pages><last>220</last><first>194</first></pages><author></author><title>Paleobiology</title></host><title>Responses of plant populations and communities to environmental changes of the Late Quaternary</title></json:item><json:item><author><json:item><name>SS Jakob</name></json:item><json:item><name>C Heibl</name></json:item><json:item><name>D Rödder</name></json:item><json:item><name>FR Blattner</name></json:item></author><host><volume>19</volume><pages><last>1438</last><first>1423</first></pages><author></author><title>Molecular Ecology</title></host><title>Population demography influences climatic niche evoluition: evidence from diploid American Hordeum species (Poaceae)</title></json:item><json:item><author><json:item><name>JM Jeschke</name></json:item><json:item><name>DL Strayer</name></json:item></author><host><volume>1134</volume><pages><last>24</last><first>1</first></pages><author></author><title>Annals of the New York Academy of Sciences</title></host><title>Usefulness of bioclimatic models for studying climate change and invasive species</title></json:item><json:item><author><json:item><name>M Kearney</name></json:item><json:item><name>W Porter</name></json:item></author><host><volume>12</volume><pages><last>350</last><first>334</first></pages><author></author><title>Ecology Letters</title></host><title>Mechanistic niche modelling: combining physiological and spatial data to predict species' ranges</title></json:item><json:item><author><json:item><name>JT Kiehl</name></json:item><json:item><name>PR Gent</name></json:item></author><host><volume>17</volume><pages><last>1669</last><first>1666</first></pages><author></author><title>Journal of Climate</title></host><title>The community climate system model, version 2</title></json:item><json:item><author><json:item><name>K King</name></json:item><json:item><name>D Cavazos</name></json:item><json:item><name>FW Judd</name></json:item></author><host><volume>39</volume><pages><last>290</last><first>289</first></pages><author></author><title>Texas Journal of Science</title></host><title>Anolis sagrei (Sauria: Iguanidae) established in southern Texas</title></json:item><json:item><author><json:item><name>JH Knouft</name></json:item><json:item><name>JB Losos</name></json:item><json:item><name>RE Glor</name></json:item><json:item><name>JJ Kolbe</name></json:item></author><host><volume>87</volume><pages><last>38</last><first>29</first></pages><author></author><title>Ecology</title></host><title>Phylogenetic analysis of the evolution of the niche in lizards of the Anolis sagrei group</title></json:item><json:item><author><json:item><name>JJ Kolbe</name></json:item><json:item><name>RE Glor</name></json:item><json:item><name>LR Schettino</name></json:item><json:item><name>AC Lara</name></json:item><json:item><name>A Larson</name></json:item><json:item><name>JB Losos</name></json:item></author><host><volume>431</volume><pages><last>181</last><first>177</first></pages><author></author><title>Nature</title></host><title>Genetic variation increases during biological invasion by a Cuban lizard</title></json:item><json:item><author><json:item><name>JJ Kolbe</name></json:item><json:item><name>RE Glor</name></json:item><json:item><name>LR Schettino</name></json:item><json:item><name>AC Lara</name></json:item><json:item><name>A Larson</name></json:item><json:item><name>JB Losos</name></json:item></author><host><volume>21</volume><pages><last>1625</last><first>1612</first></pages><author></author><title>Conservation Biology</title></host><title>Multiple sources, admixture, and genetic variation in introduced Anolis lizard populations</title></json:item><json:item><author><json:item><name>JJ Kolbe</name></json:item><json:item><name>A Larson</name></json:item><json:item><name>JB Losos</name></json:item><json:item><name>K de Queiroz</name></json:item></author><host><volume>4</volume><pages><last>437</last><first>434</first></pages><author></author><title>Biology Letters</title></host><title>Admixture determines genetic diversity and population differentiation in the biological invasion of a lizard species</title></json:item><json:item><author><json:item><name>K Kozak</name></json:item><json:item><name>JJ Wiens</name></json:item></author><host><volume>60</volume><pages><last>2621</last><first>2604</first></pages><author></author><title>Evolution</title></host><title>Does niche conservatism promote speciation? A case study in North American salamanders</title></json:item><json:item><author><json:item><name>KH Kozak</name></json:item><json:item><name>CH Graham</name></json:item><json:item><name>JJ Wiens</name></json:item></author><host><volume>23</volume><pages><last>148</last><first>141</first></pages><author></author><title>Trends in Ecology and Evolution</title></host><title>Integrating GIS‐based environmental data into evolutionary biology</title></json:item><json:item><author><json:item><name>C Kremen</name></json:item><json:item><name>A Cameron</name></json:item><json:item><name>A Moilanen</name></json:item><json:item><name>SJ Phillips</name></json:item><json:item><name>CD Thomas</name></json:item><json:item><name>H Beentje</name></json:item><json:item><name>J Dransfield</name></json:item><json:item><name>BL Fisher</name></json:item><json:item><name>F Glaw</name></json:item><json:item><name>TC Good</name></json:item><json:item><name>GJ Harper</name></json:item><json:item><name>RJ Hijmans</name></json:item><json:item><name>DC Lees</name></json:item><json:item><name>E Louis</name></json:item><json:item><name>RA Nussbaum</name></json:item><json:item><name>CJ Raxworthy</name></json:item><json:item><name>A Razafimpahanana</name></json:item><json:item><name>GE Schatz</name></json:item><json:item><name>M Vences</name></json:item><json:item><name>DR Vieites</name></json:item><json:item><name>PC Wright</name></json:item><json:item><name>ML Zjhra</name></json:item></author><host><volume>320</volume><pages><last>226</last><first>222</first></pages><author></author><title>Science</title></host><title>Aligning conservation priorities across taxa in madagascar with high‐resolution planning tools</title></json:item><json:item><author><json:item><name>CE Lee</name></json:item></author><host><volume>17</volume><pages><last>391</last><first>386</first></pages><author></author><title>Trends in Ecology and Evolution</title></host><title>Evolutionary genetics of invasive species</title></json:item><json:item><author><json:item><name>JC Lee</name></json:item></author><host><volume>44</volume><pages><last>176</last><first>171</first></pages><author></author><title>Oecologia</title></host><title>Comparative thermal ecology of two lizards</title></json:item><json:item><author><json:item><name>JC Lee</name></json:item></author><host><volume>1985</volume><pages><last>194</last><first>182</first></pages><author></author><title>Copeia</title></host><title>Anolis sagrei in Florida. Phenetics of a colonizing species. Meristic characters</title></json:item><json:item><author><json:item><name>JC Lee</name></json:item><json:item><name>D Clayton</name></json:item><json:item><name>S Eisenstein</name></json:item><json:item><name>I Perez</name></json:item></author><host><volume>1989</volume><pages><last>937</last><first>930</first></pages><author></author><title>Copeia</title></host><title>The reproductive cycle of Anolis sagrei in southern Florida</title></json:item><json:item><author><json:item><name>P Licht</name></json:item><json:item><name>GC Gorman</name></json:item></author><host><volume>95</volume><pages><last>12</last><first>1</first></pages><author></author><title>University of California Publications in Zoology</title></host><title>Reproductive and fat cycles in Caribbean Anolis lizards</title></json:item><json:item><author><json:item><name>JB Losos</name></json:item><json:item><name>JC Marks</name></json:item><json:item><name>TW Schoener</name></json:item></author><host><volume>95</volume><pages><last>532</last><first>525</first></pages><author></author><title>Oecologia</title></host><title>Habitat use and ecological interactions of an introduced and a native species of Anolis lizard on Grand Cayman, with a review of the outcomes of anole introductions</title></json:item><json:item><author><json:item><name>JB Losos</name></json:item><json:item><name>DA Spiller</name></json:item></author><host><volume>80</volume><pages><last>258</last><first>252</first></pages><author></author><title>Ecology</title></host><title>Differential colonization success and asymmetrical interactions between two lizard species</title></json:item><json:item><author><json:item><name>S Lötters</name></json:item><json:item><name>J Kielgast</name></json:item><json:item><name>J Bielby</name></json:item><json:item><name>S Schmidtlein</name></json:item><json:item><name>J Bosch</name></json:item><json:item><name>TWJ Garner</name></json:item><json:item><name>M Veith</name></json:item><json:item><name>SF Walker</name></json:item><json:item><name>MC Fisher</name></json:item><json:item><name>D Rödder</name></json:item></author><host><volume>6</volume><pages><last>372</last><first>358</first></pages><author></author><title>EcoHealth</title></host><title>The link between rapid enigmatic amphibian decline and the worldwide emerging chytrid fungus</title></json:item><json:item><author><json:item><name>S Lötters</name></json:item><json:item><name>A van der Meijden</name></json:item><json:item><name>TE Koester</name></json:item><json:item><name>T Kraus</name></json:item><json:item><name>E La Marca</name></json:item><json:item><name>CFB Haddad</name></json:item><json:item><name>D Rödder</name></json:item><json:item><name>M Veith</name></json:item></author><host><volume>19</volume><pages><last>2146</last><first>2125</first></pages><author></author><title>Biodiversity and Conservation</title></host><title>Testing vicariance versus dispersal in Amazonian harlequin frogs: an ecological niche modelling approach</title></json:item><json:item><author><json:item><name>MB Lovern</name></json:item><json:item><name>KM Passek</name></json:item></author><host><volume>80</volume><pages><last>82</last><first>77</first></pages><author></author><title>Canadian Journal of Zoology</title></host><title>Sequential alternation of offspring sex from successive eggs by female Green anoles, Anolis carolinensis</title></json:item><json:item><author><json:item><name>E Martinez‐Meyer</name></json:item></author><host><volume>2</volume><pages><last>55</last><first>42</first></pages><author></author><title>Biodiversity Informatics</title></host><title>Climate change and biodiversity: some considerations in forecasting shifts in species' potential distributions</title></json:item><json:item><host><author></author><title>McKeown S. 1996. A field guide to reptiles and amphibians in the Hawaiian Islands. Los Osos, CA: Diamond Head Publishing Inc.</title></host></json:item><json:item><author><json:item><name>H Nix</name></json:item></author><host><pages><last>15</last><first>4</first></pages><author></author><title>Atlas of elapid snakes of Australia</title></host><title>A biogeographic analysis of Australian elapid snakes</title></json:item><json:item><author><json:item><name>G Norval</name></json:item><json:item><name>J‐J Mao</name></json:item><json:item><name>H‐P Chu</name></json:item><json:item><name>C‐L Chen</name></json:item></author><host><volume>41</volume><pages><last>336</last><first>332</first></pages><author></author><title>Zoological Studies</title></host><title>A new record of an introduced species, the brown anole (Anolis sagrei) (Duméril and Bibron, 1837), in Taiwan</title></json:item><json:item><author><json:item><name>BL Otto‐Bliesner</name></json:item><json:item><name>EC Brady</name></json:item><json:item><name>G Clauzet</name></json:item><json:item><name>R Tomas</name></json:item><json:item><name>S Levis</name></json:item><json:item><name>Z Kothavala</name></json:item></author><host><volume>19</volume><pages><last>2544</last><first>2526</first></pages><author></author><title>Journal of Climate</title></host><title>Last glacial maximum and holocene climate in CCSM3</title></json:item><json:item><author><json:item><name>MJ Pansza</name></json:item><json:item><name>R Powell</name></json:item></author><host><volume>36</volume><pages><first>201</first></pages><author></author><title>Herpetological Review</title></host><title>Geographic distribution: Anolis carolinensis (green anole)</title></json:item><json:item><author><json:item><name>D Parmley</name></json:item></author><host><volume>4</volume><pages><first>191</first></pages><author></author><title>Georgia Journal of Science</title></host><title>Northernmost record of the brown anole (Anolis sagrei) in Georgia</title></json:item><json:item><author><json:item><name>PB Pearman</name></json:item><json:item><name>A Guisan</name></json:item><json:item><name>O Broennimann</name></json:item><json:item><name>CF Randin</name></json:item></author><host><volume>23</volume><pages><last>158</last><first>149</first></pages><author></author><title>Trends in Ecology and Evolution</title></host><title>Niche dynamics in space and time</title></json:item><json:item><author><json:item><name>RG Pearson</name></json:item><json:item><name>CJ Raxworthy</name></json:item><json:item><name>M Nakamura</name></json:item><json:item><name>AT Peterson</name></json:item></author><host><volume>34</volume><pages><last>117</last><first>102</first></pages><author></author><title>Journal of Biogeography</title></host><title>Predicting species distributions from small numbers of occurrence records: a test case using cryptic geckos in Madagascar</title></json:item><json:item><author><json:item><name>AT Peterson</name></json:item><json:item><name>Y Nakazawa</name></json:item></author><host><volume>17</volume><pages><last>144</last><first>135</first></pages><author></author><title>Global Ecology and Biogeography</title></host><title>Environmental data sets matter in ecological niche modelling: an example with Solenopsis invicta and Solenopsis richteri</title></json:item><json:item><author><json:item><name>AT Peterson</name></json:item><json:item><name>ÁS Nyári</name></json:item></author><host><volume>62</volume><pages><last>183</last><first>173</first></pages><author></author><title>Evolution</title></host><title>Ecological niche conservatism and Pleistocene refugia in the thrush‐like mourner, Shiffornis sp., in the Neotropics</title></json:item><json:item><author><json:item><name>AT Peterson</name></json:item><json:item><name>J Soberón</name></json:item><json:item><name>V Sánchez‐Cordero</name></json:item></author><host><volume>285</volume><pages><last>1267</last><first>1265</first></pages><author></author><title>Science</title></host><title>Conservation of ecological niches in evolutionary time</title></json:item><json:item><author><json:item><name>AT Peterson</name></json:item><json:item><name>DA Vieglais</name></json:item></author><host><volume>51</volume><pages><last>371</last><first>363</first></pages><author></author><title>BioScience</title></host><title>Predicting species invasions using ecological niche modelling: new approaches from bioinformatics attack a pressing problem</title></json:item><json:item><author><json:item><name>SJ Phillips</name></json:item></author><host><volume>31</volume><pages><last>278</last><first>272</first></pages><author></author><title>Ecography</title></host><title>Transferability, sample selection bias and background data in presence‐only modelling: a response to Peterson et al. (2007)</title></json:item><json:item><author><json:item><name>SJ Phillips</name></json:item><json:item><name>RP Anderson</name></json:item><json:item><name>RE Schapire</name></json:item></author><host><volume>190</volume><pages><last>259</last><first>231</first></pages><author></author><title>Ecological Modelling</title></host><title>Maximum entropy modelling of species geographic distributions</title></json:item><json:item><author><json:item><name>SJ Phillips</name></json:item><json:item><name>M Dudík</name></json:item></author><host><volume>31</volume><pages><last>175</last><first>161</first></pages><author></author><title>Ecography</title></host><title>Modelling of species distributions with Maxent: new extensions and comprehensive evaluation</title></json:item><json:item><author><json:item><name>R Puschendorf</name></json:item><json:item><name>AC Carnaval</name></json:item><json:item><name>J Vanderwal</name></json:item><json:item><name>H Zumbado‐Ulate</name></json:item><json:item><name>G Chaves</name></json:item><json:item><name>F Bolaños</name></json:item><json:item><name>RA Alford</name></json:item></author><host><volume>15</volume><pages><last>408</last><first>401</first></pages><author></author><title>Diversity and Distributions</title></host><title>Distribution models for the amphibian chytrid Batrachochytrium dendrobatidis in Costa Rica: proposing climatic refuges as a conservation tool</title></json:item><json:item><author><json:item><name>GH Rodda</name></json:item><json:item><name>TH Fritts</name></json:item><json:item><name>MJ McCoid</name></json:item><json:item><name>EW Campbell</name></json:item></author><host><pages><last>80</last><first>44</first></pages><author></author><title>Problem snake management: the habu and the brown treesnake</title></host><title>An overview of the biology of the brown treesnake (Boiga irregularis), a costly introduced pest on Pacific islands</title></json:item><json:item><author><json:item><name>D Rödder</name></json:item><json:item><name>JO Engler</name></json:item></author><host><author></author><title>Global Ecology and Biogeography</title></host><title>Quantitative metrics of overlaps in Grinnellian niches: advances and possible drawbacks</title></json:item><json:item><author><json:item><name>D Rödder</name></json:item><json:item><name>J Kielgast</name></json:item><json:item><name>J Bielby</name></json:item><json:item><name>S Schmidtlein</name></json:item><json:item><name>J Bosch</name></json:item><json:item><name>TWJ Garner</name></json:item><json:item><name>M Veith</name></json:item><json:item><name>S Walker</name></json:item><json:item><name>MC Fisher</name></json:item><json:item><name>S Lötters</name></json:item></author><host><volume>1</volume><pages><last>66</last><first>52</first></pages><author></author><title>Diversity</title></host><title>Global amphibian extinction risk assessment for the panzootic chytrid fungus</title></json:item><json:item><author><json:item><name>D Rödder</name></json:item><json:item><name>A Kwet</name></json:item><json:item><name>S Lötters</name></json:item></author><host><volume>43</volume><pages><last>2536</last><first>2525</first></pages><author></author><title>Journal of Natural History</title></host><title>Translating natural history into geographic space: a macroecological perspective on the North American slider, Trachemys scripta (Reptilia, Cryptodira, Emydidae)</title></json:item><json:item><author><json:item><name>D Rödder</name></json:item><json:item><name>S Lötters</name></json:item></author><host><volume>18</volume><pages><last>687</last><first>674</first></pages><author></author><title>Global Ecology and Biogeography</title></host><title>Niche shift versus niche conservatism? Climatic charactersitics of the native and invasive ranges of the Mediterranean house gecko (Hemidactylus turcicus)</title></json:item><json:item><author><json:item><name>D Rödder</name></json:item><json:item><name>S Lötters</name></json:item></author><host><volume>97</volume><pages><last>796</last><first>781</first></pages><author></author><title>Die Naturwissenschaften</title></host><title>Explanative power of variables used in Species Distribution Modelling: an issue of general model transferability or niche shift in the invasive greenhouse frog (Eleutherodactylus planirostris)?</title></json:item><json:item><author><json:item><name>D Rödder</name></json:item><json:item><name>M Solé</name></json:item><json:item><name>W Böhme</name></json:item></author><host><volume>4</volume><pages><last>246</last><first>236</first></pages><author></author><title>North-Western Journal of Zoology</title></host><title>Predicting the potential distribution of two alien invasive housegeckos (Gekkonidae: Hemidactylus frenatus, Hemidactylus mabouia)</title></json:item><json:item><author><json:item><name>JP Rodríguez</name></json:item><json:item><name>L Brotons</name></json:item><json:item><name>J Busatamante</name></json:item><json:item><name>J Seoane</name></json:item></author><host><volume>13</volume><pages><last>251</last><first>243</first></pages><author></author><title>Diversity and Distributions</title></host><title>The application of predictive modelling of species distribution to biodiversity conservation</title></json:item><json:item><author><json:item><name>JA Rodríguez‐Robles</name></json:item><json:item><name>T Jezkova</name></json:item><json:item><name>M Leal</name></json:item></author><host><volume>19</volume><pages><last>1876</last><first>1860</first></pages><author></author><title>Molecular Ecology</title></host><title>Climatic stability and genetic divergence in the tropical insular lizard Anolis krugi, the Puerto Rican ‘Lagertijo Jardinero de la Montaña’</title></json:item><json:item><author><json:item><name>GL Rogowitz</name></json:item></author><host><volume>21</volume><pages><last>14</last><first>11</first></pages><author></author><title>Journal of Thermal Biology</title></host><title>Evaluation of thermal acclimatisation of metabolism in two eurythermal lizards, Anolis cristatellus and A. sagrei</title></json:item><json:item><author><json:item><name>D Sax</name></json:item><json:item><name>J Stachowicz</name></json:item><json:item><name>J Brown</name></json:item><json:item><name>JF Bruno</name></json:item><json:item><name>MN Dawson</name></json:item><json:item><name>SD Gaines</name></json:item><json:item><name>RK Grosberg</name></json:item><json:item><name>A Hastings</name></json:item><json:item><name>RD Holt</name></json:item><json:item><name>M Mayfield</name></json:item><json:item><name>MI O'Connor</name></json:item><json:item><name>WR Rice</name></json:item></author><host><volume>22</volume><pages><last>471</last><first>465</first></pages><author></author><title>Trends in Ecology and Evolution</title></host><title>Ecological and evolutionary insights from species invasions</title></json:item><json:item><author><json:item><name>TW Schoener</name></json:item></author><host><volume>49</volume><pages><last>726</last><first>704</first></pages><author></author><title>Ecology</title></host><title>Anolis lizards of Bimini – resource partitioning in a complex fauna</title></json:item><json:item><host><author></author><title>Schwartz A, Henderson RW. 1991. Amphibians and reptiles of the West Indies: descriptions, distributions, and natural history. Gainesville, FL: University of Florida Press.</title></host></json:item><json:item><author><json:item><name>OJ Sexton</name></json:item><json:item><name>KM Brown</name></json:item></author><host><volume>11</volume><pages><last>250</last><first>241</first></pages><author></author><title>Journal of Natural History</title></host><title>The reproductive cycle of an iguanid lizard Anolis sagrei, from Belize</title></json:item><json:item><author><json:item><name>J Soberón</name></json:item><json:item><name>AT Peterson</name></json:item></author><host><volume>2</volume><pages><last>10</last><first>1</first></pages><author></author><title>Biodiversity Informatics</title></host><title>Interpretation of models of fundamental ecological niches and species' distributional areas</title></json:item><json:item><author><json:item><name>FM Steiner</name></json:item><json:item><name>BC Schlick‐Steiner</name></json:item><json:item><name>J VanDerWal</name></json:item><json:item><name>KD Reuther</name></json:item><json:item><name>E Christian</name></json:item><json:item><name>C Stauffer</name></json:item><json:item><name>AV Suarez</name></json:item><json:item><name>SE Williams</name></json:item><json:item><name>RH Crozier</name></json:item></author><host><volume>14</volume><pages><last>545</last><first>538</first></pages><author></author><title>Diversity and Distributions</title></host><title>Combined modelling of distribution and niche in invasion biology: a case study of two invasive Teramorium ant species</title></json:item><json:item><author><json:item><name>K Swets</name></json:item></author><host><volume>240</volume><pages><last>1293</last><first>1285</first></pages><author></author><title>Science</title></host><title>Measuring the accuracy of diagnostic systems</title></json:item><json:item><author><json:item><name>FH Van Berkum</name></json:item></author><host><volume>40</volume><pages><last>604</last><first>594</first></pages><author></author><title>Evolution</title></host><title>Evolutionary patterns of the thermal sensitivity of sprint speed in Anolis lizards</title></json:item><json:item><author><json:item><name>FH Van Berkum</name></json:item></author><host><volume>132</volume><pages><last>343</last><first>327</first></pages><author></author><title>American Naturalist</title></host><title>Latitudinal patterns of the thermal sensitivity of sprint speed in lizards</title></json:item><json:item><author><json:item><name>BE Viets</name></json:item><json:item><name>MA Ewert</name></json:item><json:item><name>LG Talent</name></json:item><json:item><name>CE Nelson</name></json:item></author><host><volume>270</volume><pages><last>56</last><first>45</first></pages><author></author><title>Journal of Experimental Zoology</title></host><title>Sex‐determining mechanisms in squamate reptiles</title></json:item><json:item><author><json:item><name>DL Warren</name></json:item><json:item><name>RE Glor</name></json:item><json:item><name>M Turelli</name></json:item></author><host><volume>62</volume><pages><last>2883</last><first>2868</first></pages><author></author><title>Evolution</title></host><title>Environmental niche equivalency versus conservatism: quantitative approaches to niche evolution</title></json:item><json:item><author><json:item><name>JJ Wiens</name></json:item><json:item><name>CH Graham</name></json:item></author><host><volume>36</volume><pages><last>539</last><first>519</first></pages><author></author><title>Annual Review in Ecology and Systematics</title></host><title>Niche conservatism: integrating evolution, ecology, and conservation biology</title></json:item><json:item><author><json:item><name>EE Williams</name></json:item></author><host><volume>44</volume><pages><last>389</last><first>345</first></pages><author></author><title>Quarternary Review in Biology</title></host><title>The ecology of colonization as seen in the zoogeography of anoline lizards on small islands</title></json:item></refBibs><genre><json:string>article</json:string></genre><host><volume>104</volume><publisherId><json:string>BIJ</json:string></publisherId><pages><total>12</total><last>954</last><first>943</first></pages><issn><json:string>0024-4066</json:string></issn><issue>4</issue><genre><json:string>journal</json:string></genre><language><json:string>unknown</json:string></language><eissn><json:string>1095-8312</json:string></eissn><title>Biological Journal of the Linnean Society</title><doi><json:string>10.1111/(ISSN)1095-8312</json:string></doi></host><categories><wos><json:string>science</json:string><json:string>evolutionary biology</json:string></wos><scienceMetrix><json:string>natural sciences</json:string><json:string>biology</json:string><json:string>evolutionary biology</json:string></scienceMetrix></categories><publicationDate>2011</publicationDate><copyrightDate>2011</copyrightDate><doi><json:string>10.1111/j.1095-8312.2011.01780.x</json:string></doi><id>44EFAAE005DC9F955A066BE4BE5B360C1AE08749</id><score>1.5713098</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/44EFAAE005DC9F955A066BE4BE5B360C1AE08749/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/44EFAAE005DC9F955A066BE4BE5B360C1AE08749/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/44EFAAE005DC9F955A066BE4BE5B360C1AE08749/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Climate niche shift in invasive species: the case of the brown anole</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><availability><p>© 2011 The Linnean Society of London</p></availability><date>2011</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Climate niche shift in invasive species: the case of the brown anole</title><author xml:id="author-1"><persName><forename type="first">LEA‐SU</forename><surname>ANGETTER</surname></persName><affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</affiliation></author><author xml:id="author-2"><persName><forename type="first">STEFAN</forename><surname>LÖTTERS</surname></persName><affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</affiliation></author><author xml:id="author-3"><persName><forename type="first">DENNIS</forename><surname>RÖDDER</surname></persName><email>d.roedder.zfmk@uni‐bonn.de</email><affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</affiliation><affiliation>Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany</affiliation></author></analytic><monogr><title level="j">Biological Journal of the Linnean Society</title><idno type="pISSN">0024-4066</idno><idno type="eISSN">1095-8312</idno><idno type="DOI">10.1111/(ISSN)1095-8312</idno><imprint><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2011-12"></date><biblScope unit="volume">104</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="943">943</biblScope><biblScope unit="page" to="954">954</biblScope></imprint></monogr><idno type="istex">44EFAAE005DC9F955A066BE4BE5B360C1AE08749</idno><idno type="DOI">10.1111/j.1095-8312.2011.01780.x</idno><idno type="ArticleID">BIJ1780</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2011</date></creation><langUsage><language ident="en">en</language></langUsage><abstract><p>Anolis sagrei, a Cuba and Bahama native lizard, is a successful invader in Florida and adjacent areas. Herein, we focus on conservatism in its climate niche axes and possible congruencies with its natural history properties. The not mutually exclusive hypotheses of the present study explaining its northern range limit are: (1) climatic conditions within species' native and invasive ranges are identical; (2) the species is pre‐adapted to novel conditions as a result of historical climate variations; and (3) only some niche axes limit the species' invasive distribution and the observed pattern is explained by an interplay between the potential niche within its native range and life‐history. Species distribution models for native and invasive distributions were built on ten bioclimatic variables. Using Schoener's niche overlap index, the degree of niche conservatism among variables was identified. Significances of hypothesis (1) were tested using null‐model approaches. Possible climatic pre‐adaptations were evaluated by comparing its actual tolerance within its invasive range with that of the Last Glacial Maximum (LGM) within its native range (hypothesis 2). Results of (1) and (2) are discussed in relation to natural history, approaching hypothesis 3. We detect varying overlaps in niche axes, indicating that natural history properties are associated with conservative niche axes. Climatic comparisons with LGM of native and current conditions of invasive range suggest that pre‐adaptations are unlikely. Possible shifts in the fundamental niche of the species may have been facilitated by enhanced genetic diversity in northern invasive populations. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 104, 943–954.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>keywords</head><item><term>Anolis sagrei</term></item><item><term>bioclimatic variables</term></item><item><term>historical climate variation</term></item><item><term>last glacial maximum</term></item><item><term>maxent</term></item><item><term>species distribution model</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2011-12">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/44EFAAE005DC9F955A066BE4BE5B360C1AE08749/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1095-8312</doi><issn type="print">0024-4066</issn><issn type="electronic">1095-8312</issn><idGroup><id type="product" value="BIJ"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="BIOLOGICAL JOURNAL LINNEAN SOCIETY">Biological Journal of the Linnean Society</title></titleGroup></publicationMeta><publicationMeta level="part" position="12104"><doi origin="wiley">10.1111/bij.2011.104.issue-4</doi><numberingGroup><numbering type="journalVolume" number="104">104</numbering><numbering type="journalIssue" number="4">4</numbering></numberingGroup><coverDate startDate="2011-12">December 2011</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="17" status="forIssue"><doi origin="wiley">10.1111/j.1095-8312.2011.01780.x</doi><idGroup><id type="unit" value="BIJ1780"></id></idGroup><countGroup><count type="pageTotal" number="12"></count></countGroup><titleGroup><title type="tocHeading1">Original Articles</title></titleGroup><copyright>© 2011 The Linnean Society of London</copyright><eventGroup><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.10 mode:FullText" date="2011-10-27"></event><event type="publishedOnlineEarlyUnpaginated" date="2011-10-07"></event><event type="firstOnline" date="2011-10-07"></event><event type="publishedOnlineFinalForm" date="2011-10-27"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-22"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-15"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="943">943</numbering><numbering type="pageLast" number="954">954</numbering></numberingGroup><correspondenceTo> E‐mail: <email normalForm="d.roedder.zfmk@uni-bonn.de">d.roedder.zfmk@uni‐bonn.de</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:BIJ.BIJ1780.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received 12 January 2011; revised 1 July 2011; accepted for publication 1 July 2011</unparsedEditorialHistory><countGroup><count type="figureTotal" number="2"></count><count type="tableTotal" number="1"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="106"></count><count type="wordTotal" number="8622"></count><count type="linksPubMed" number="0"></count><count type="linksCrossRef" number="0"></count></countGroup><titleGroup><title type="main">Climate niche shift in invasive species: the case of the brown anole</title><title type="shortAuthors">L.‐S. ANGETTER <i>ET AL</i>.</title><title type="short">CLIMATE NICHE SHIFT IN A LIZARD</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>LEA‐SU</givenNames><familyName>ANGETTER</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>STEFAN</givenNames><familyName>LÖTTERS</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1 #a2" corresponding="yes"><personName><givenNames>DENNIS</givenNames><familyName>RÖDDER</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="DE"><unparsedAffiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="DE"><unparsedAffiliation>Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1"><i>Anolis sagrei</i></keyword><keyword xml:id="k2">bioclimatic variables</keyword><keyword xml:id="k3">historical climate variation</keyword><keyword xml:id="k4">last glacial maximum</keyword><keyword xml:id="k5">maxent</keyword><keyword xml:id="k6">species distribution model</keyword></keywordGroup><supportingInformation><p><b>Table S1.</b> Correlation matrix of bioclimatic values (Pearson's <i>R<sup>2</sup></i>) within the study area. bio1, annual mean temperature; bio2, mean diurnal range [mean of monthly (maximum temp – minimum temp)]; bio3, isothermality (bio2/bio7) (* 100); bio4, temperature seasonality (SD × 100); bio5, maximum temperature of warmest month; bio6, minimum temperature of coldest month; bio7, temperature annual range (bio5 – bio6); bio8, mean temperature of wettest quarter; bio9, mean temperature of driest quarter; bio10, mean temperature of warmest quarter; bio11, mean temperature of coldest quarter; bio12, annual precipitation; bio13, precipitation of wettest month; bio14, precipitation of driest month; bio15, precipitation seasonality (coefficient of variation); bio16, precipitation of wettest quarter; bio17, precipitation of driest quarter; bio18, precipitation of warmest quarter; bio19, precipitation of coldest quarter.</p><p><b>Table S2.</b> Area under the curve (AUC) values per model developed with species records filtered in environmental space in order to reduce possible autocorrelation effects, niche overlap, similarity and identity in terms of Schoener's index (<i>D</i>) values and assessment of niche similarity and equivalency via randomization tests (see text). nat, native; inv, invasive; ns, not significant. Values in which observed (OBS) overlap is higher than the null distribution are shown in bold and values in which overlap is lower are in italics. Note that AUC values are only comparable within the native or invasive samples because they depend on the number of records used for computations and the extent of the study area.</p><supportingInfoItem><mediaResource alt="supporting info item" href="urn-x:wiley:00244066:media:bij1780:BIJ_1780_sm_TabS1-2"></mediaResource><caption>Supporting info item</caption></supportingInfoItem></supportingInformation><abstractGroup><abstract type="main" xml:lang="en"><p><i>Anolis sagrei</i>, a Cuba and Bahama native lizard, is a successful invader in Florida and adjacent areas. Herein, we focus on conservatism in its climate niche axes and possible congruencies with its natural history properties. The not mutually exclusive hypotheses of the present study explaining its northern range limit are: (1) climatic conditions within species' native and invasive ranges are identical; (2) the species is pre‐adapted to novel conditions as a result of historical climate variations; and (3) only some niche axes limit the species' invasive distribution and the observed pattern is explained by an interplay between the potential niche within its native range and life‐history. Species distribution models for native and invasive distributions were built on ten bioclimatic variables. Using Schoener's niche overlap index, the degree of niche conservatism among variables was identified. Significances of hypothesis (1) were tested using null‐model approaches. Possible climatic pre‐adaptations were evaluated by comparing its actual tolerance within its invasive range with that of the Last Glacial Maximum (LGM) within its native range (hypothesis 2). Results of (1) and (2) are discussed in relation to natural history, approaching hypothesis 3. We detect varying overlaps in niche axes, indicating that natural history properties are associated with conservative niche axes. Climatic comparisons with LGM of native and current conditions of invasive range suggest that pre‐adaptations are unlikely. Possible shifts in the fundamental niche of the species may have been facilitated by enhanced genetic diversity in northern invasive populations. © 2011 The Linnean Society of London, <i>Biological Journal of the Linnean Society</i>, 2011, <b>104</b>, 943–954.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Climate niche shift in invasive species: the case of the brown anole</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>CLIMATE NICHE SHIFT IN A LIZARD</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Climate niche shift in invasive species: the case of the brown anole</title></titleInfo><name type="personal"><namePart type="given">LEA‐SU</namePart><namePart type="family">ANGETTER</namePart><affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">STEFAN</namePart><namePart type="family">LÖTTERS</namePart><affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">DENNIS</namePart><namePart type="family">RÖDDER</namePart><affiliation>Department of Biogeography, Trier University, 54286 Trier, Germany</affiliation><affiliation>Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany</affiliation><affiliation>E-mail: d.roedder.zfmk@uni‐bonn.de</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2011-12</dateIssued><edition>Received 12 January 2011; revised 1 July 2011; accepted for publication 1 July 2011</edition><copyrightDate encoding="w3cdtf">2011</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">2</extent><extent unit="tables">1</extent><extent unit="references">106</extent><extent unit="words">8622</extent></physicalDescription><abstract>Anolis sagrei, a Cuba and Bahama native lizard, is a successful invader in Florida and adjacent areas. Herein, we focus on conservatism in its climate niche axes and possible congruencies with its natural history properties. The not mutually exclusive hypotheses of the present study explaining its northern range limit are: (1) climatic conditions within species' native and invasive ranges are identical; (2) the species is pre‐adapted to novel conditions as a result of historical climate variations; and (3) only some niche axes limit the species' invasive distribution and the observed pattern is explained by an interplay between the potential niche within its native range and life‐history. Species distribution models for native and invasive distributions were built on ten bioclimatic variables. Using Schoener's niche overlap index, the degree of niche conservatism among variables was identified. Significances of hypothesis (1) were tested using null‐model approaches. Possible climatic pre‐adaptations were evaluated by comparing its actual tolerance within its invasive range with that of the Last Glacial Maximum (LGM) within its native range (hypothesis 2). Results of (1) and (2) are discussed in relation to natural history, approaching hypothesis 3. We detect varying overlaps in niche axes, indicating that natural history properties are associated with conservative niche axes. Climatic comparisons with LGM of native and current conditions of invasive range suggest that pre‐adaptations are unlikely. Possible shifts in the fundamental niche of the species may have been facilitated by enhanced genetic diversity in northern invasive populations. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 104, 943–954.</abstract><subject lang="en"><genre>keywords</genre><topic>Anolis sagrei</topic><topic>bioclimatic variables</topic><topic>historical climate variation</topic><topic>last glacial maximum</topic><topic>maxent</topic><topic>species distribution model</topic></subject><relatedItem type="host"><titleInfo><title>Biological Journal of the Linnean Society</title></titleInfo><genre type="journal">journal</genre><note type="content"> Table S1. Correlation matrix of bioclimatic values (Pearson's R2) within the study area. bio1, annual mean temperature; bio2, mean diurnal range [mean of monthly (maximum temp – minimum temp)]; bio3, isothermality (bio2/bio7) (* 100); bio4, temperature seasonality (SD × 100); bio5, maximum temperature of warmest month; bio6, minimum temperature of coldest month; bio7, temperature annual range (bio5 – bio6); bio8, mean temperature of wettest quarter; bio9, mean temperature of driest quarter; bio10, mean temperature of warmest quarter; bio11, mean temperature of coldest quarter; bio12, annual precipitation; bio13, precipitation of wettest month; bio14, precipitation of driest month; bio15, precipitation seasonality (coefficient of variation); bio16, precipitation of wettest quarter; bio17, precipitation of driest quarter; bio18, precipitation of warmest quarter; bio19, precipitation of coldest quarter. Table S2. Area under the curve (AUC) values per model developed with species records filtered in environmental space in order to reduce possible autocorrelation effects, niche overlap, similarity and identity in terms of Schoener's index (D) values and assessment of niche similarity and equivalency via randomization tests (see text). nat, native; inv, invasive; ns, not significant. Values in which observed (OBS) overlap is higher than the null distribution are shown in bold and values in which overlap is lower are in italics. Note that AUC values are only comparable within the native or invasive samples because they depend on the number of records used for computations and the extent of the study area. Table S1. Correlation matrix of bioclimatic values (Pearson's R2) within the study area. bio1, annual mean temperature; bio2, mean diurnal range [mean of monthly (maximum temp – minimum temp)]; bio3, isothermality (bio2/bio7) (* 100); bio4, temperature seasonality (SD × 100); bio5, maximum temperature of warmest month; bio6, minimum temperature of coldest month; bio7, temperature annual range (bio5 – bio6); bio8, mean temperature of wettest quarter; bio9, mean temperature of driest quarter; bio10, mean temperature of warmest quarter; bio11, mean temperature of coldest quarter; bio12, annual precipitation; bio13, precipitation of wettest month; bio14, precipitation of driest month; bio15, precipitation seasonality (coefficient of variation); bio16, precipitation of wettest quarter; bio17, precipitation of driest quarter; bio18, precipitation of warmest quarter; bio19, precipitation of coldest quarter. Table S2. Area under the curve (AUC) values per model developed with species records filtered in environmental space in order to reduce possible autocorrelation effects, niche overlap, similarity and identity in terms of Schoener's index (D) values and assessment of niche similarity and equivalency via randomization tests (see text). nat, native; inv, invasive; ns, not significant. Values in which observed (OBS) overlap is higher than the null distribution are shown in bold and values in which overlap is lower are in italics. Note that AUC values are only comparable within the native or invasive samples because they depend on the number of records used for computations and the extent of the study area.Supporting Info Item: Supporting info item - </note><identifier type="ISSN">0024-4066</identifier><identifier type="eISSN">1095-8312</identifier><identifier type="DOI">10.1111/(ISSN)1095-8312</identifier><identifier type="PublisherID">BIJ</identifier><part><date>2011</date><detail type="volume"><caption>vol.</caption><number>104</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>943</start><end>954</end><total>12</total></extent></part></relatedItem><identifier type="istex">44EFAAE005DC9F955A066BE4BE5B360C1AE08749</identifier><identifier type="DOI">10.1111/j.1095-8312.2011.01780.x</identifier><identifier type="ArticleID">BIJ1780</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2011 The Linnean Society of London</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Rhénanie/explor/UnivTrevesV1/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001A22 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 001A22 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Rhénanie
|area= UnivTrevesV1
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:44EFAAE005DC9F955A066BE4BE5B360C1AE08749
|texte= Climate niche shift in invasive species: the case of the brown anole
}}
| This area was generated with Dilib version V0.6.31. |  |