Forelimb-hindlimb developmental timing changes across tetrapod phylogeny
Identifieur interne : 001084 ( Pmc/Corpus ); précédent : 001083; suivant : 001085Forelimb-hindlimb developmental timing changes across tetrapod phylogeny
Auteurs : Olaf Rp Bininda-Emonds ; Jonathan E. Jeffery ; Marcelo R. Sánchez-Villagra ; James Hanken ; Matthew Colbert ; Claude Pieau ; Lynne Selwood ; Carel Ten Cate ; Albert Raynaud ; Casmile K. Osabutey ; Michael K. RichardsonSource :
- BMC Evolutionary Biology [ 1471-2148 ] ; 2007.
Abstract
Tetrapods exhibit great diversity in limb structures among species and also between forelimbs and hindlimbs within species, diversity which frequently correlates with locomotor modes and life history. We aim to examine the potential relation of changes in developmental timing (heterochrony) to the origin of limb morphological diversity in an explicit comparative and quantitative framework. In particular, we studied the relative time sequence of development of the forelimbs versus the hindlimbs in 138 embryos of 14 tetrapod species spanning a diverse taxonomic, ecomorphological and life-history breadth. Whole-mounts and histological sections were used to code the appearance of 10 developmental events comprising landmarks of development from the early bud stage to late chondrogenesis in the forelimb and the corresponding serial homologues in the hindlimb.
An overall pattern of change across tetrapods can be discerned and appears to be relatively clade-specific. In the primitive condition, as seen in Chondrichthyes and Osteichthyes, the forelimb/pectoral fin develops earlier than the hindlimb/pelvic fin. This pattern is either retained or re-evolved in eulipotyphlan insectivores (= shrews, moles, hedgehogs, and solenodons) and taken to its extreme in marsupials. Although exceptions are known, the two anurans we examined reversed the pattern and displayed a significant advance in hindlimb development. All other species examined, including a bat with its greatly enlarged forelimbs modified as wings in the adult, showed near synchrony in the development of the fore and hindlimbs.
Major heterochronic changes in early limb development and chondrogenesis were absent within major clades except Lissamphibia, and their presence across vertebrate phylogeny are not easily correlated with adaptive phenomena related to morphological differences in the adult fore- and hindlimbs. The apparently conservative nature of this trait means that changes in chondrogenetic patterns may serve as useful phylogenetic characters at higher taxonomic levels in tetrapods. Our results highlight the more important role generally played by allometric heterochrony in this instance to shape adult morphology.
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DOI: 10.1186/1471-2148-7-182
PubMed: 17908305
PubMed Central: 2194785
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Forelimb-hindlimb developmental timing changes across tetrapod phylogeny</title><author><name sortKey="Bininda Emonds, Olaf Rp" sort="Bininda Emonds, Olaf Rp" uniqKey="Bininda Emonds O" first="Olaf Rp" last="Bininda-Emonds">Olaf Rp Bininda-Emonds</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Institut für Spezielle Zoologie und Evolutionsbiologie mit Phyletischem Museum, Friedrich-Schiller-Universität Jena, Erbertstrasse 1, 07743 Jena, Germany</nlm:aff></affiliation></author><author><name sortKey="Jeffery, Jonathan E" sort="Jeffery, Jonathan E" uniqKey="Jeffery J" first="Jonathan E" last="Jeffery">Jonathan E. Jeffery</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Sanchez Villagra, Marcelo R" sort="Sanchez Villagra, Marcelo R" uniqKey="Sanchez Villagra M" first="Marcelo R" last="Sánchez-Villagra">Marcelo R. Sánchez-Villagra</name><affiliation><nlm:aff id="I3">Palaeontologisches Institut und Museum, Karl Schmid-Strasse 4, CH-8006 Zürich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Hanken, James" sort="Hanken, James" uniqKey="Hanken J" first="James" last="Hanken">James Hanken</name><affiliation><nlm:aff id="I4">Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA</nlm:aff></affiliation></author><author><name sortKey="Colbert, Matthew" sort="Colbert, Matthew" uniqKey="Colbert M" first="Matthew" last="Colbert">Matthew Colbert</name><affiliation><nlm:aff id="I5">Department of Geological Sciences, The University of Texas, Austin, TX 78712, USA</nlm:aff></affiliation></author><author><name sortKey="Pieau, Claude" sort="Pieau, Claude" uniqKey="Pieau C" first="Claude" last="Pieau">Claude Pieau</name><affiliation><nlm:aff id="I6">Laboratoire de Biochimie du Développement, Institut Jacques Monod, CNRS et Université Paris 6 et 7, Tour 43-33, E3, 2, place Jussieu, 75251 Paris Cedex 05, France</nlm:aff></affiliation></author><author><name sortKey="Selwood, Lynne" sort="Selwood, Lynne" uniqKey="Selwood L" first="Lynne" last="Selwood">Lynne Selwood</name><affiliation><nlm:aff id="I7">Department of Zoology, Gate 12, University of Melbourne, Victoria. 3010, Australia</nlm:aff></affiliation></author><author><name sortKey="Ten Cate, Carel" sort="Ten Cate, Carel" uniqKey="Ten Cate C" first="Carel" last="Ten Cate">Carel Ten Cate</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Raynaud, Albert" sort="Raynaud, Albert" uniqKey="Raynaud A" first="Albert" last="Raynaud">Albert Raynaud</name><affiliation><nlm:aff id="I8">Formerly of Laboratoire Pasteur (Embryologie expérimentale), 20 rue des Moulins, 95110 Sannois, France</nlm:aff></affiliation></author><author><name sortKey="Osabutey, Casmile K" sort="Osabutey, Casmile K" uniqKey="Osabutey C" first="Casmile K" last="Osabutey">Casmile K. Osabutey</name><affiliation><nlm:aff id="I9">Department of Anatomy, St George's Hospital Medical School, Tooting, London SW17 0RE, UK</nlm:aff></affiliation></author><author><name sortKey="Richardson, Michael K" sort="Richardson, Michael K" uniqKey="Richardson M" first="Michael K" last="Richardson">Michael K. Richardson</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">17908305</idno><idno type="pmc">2194785</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194785</idno><idno type="RBID">PMC:2194785</idno><idno type="doi">10.1186/1471-2148-7-182</idno><date when="2007">2007</date><idno type="wicri:Area/Pmc/Corpus">001084</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001084</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Forelimb-hindlimb developmental timing changes across tetrapod phylogeny</title><author><name sortKey="Bininda Emonds, Olaf Rp" sort="Bininda Emonds, Olaf Rp" uniqKey="Bininda Emonds O" first="Olaf Rp" last="Bininda-Emonds">Olaf Rp Bininda-Emonds</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Institut für Spezielle Zoologie und Evolutionsbiologie mit Phyletischem Museum, Friedrich-Schiller-Universität Jena, Erbertstrasse 1, 07743 Jena, Germany</nlm:aff></affiliation></author><author><name sortKey="Jeffery, Jonathan E" sort="Jeffery, Jonathan E" uniqKey="Jeffery J" first="Jonathan E" last="Jeffery">Jonathan E. Jeffery</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Sanchez Villagra, Marcelo R" sort="Sanchez Villagra, Marcelo R" uniqKey="Sanchez Villagra M" first="Marcelo R" last="Sánchez-Villagra">Marcelo R. Sánchez-Villagra</name><affiliation><nlm:aff id="I3">Palaeontologisches Institut und Museum, Karl Schmid-Strasse 4, CH-8006 Zürich, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Hanken, James" sort="Hanken, James" uniqKey="Hanken J" first="James" last="Hanken">James Hanken</name><affiliation><nlm:aff id="I4">Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA</nlm:aff></affiliation></author><author><name sortKey="Colbert, Matthew" sort="Colbert, Matthew" uniqKey="Colbert M" first="Matthew" last="Colbert">Matthew Colbert</name><affiliation><nlm:aff id="I5">Department of Geological Sciences, The University of Texas, Austin, TX 78712, USA</nlm:aff></affiliation></author><author><name sortKey="Pieau, Claude" sort="Pieau, Claude" uniqKey="Pieau C" first="Claude" last="Pieau">Claude Pieau</name><affiliation><nlm:aff id="I6">Laboratoire de Biochimie du Développement, Institut Jacques Monod, CNRS et Université Paris 6 et 7, Tour 43-33, E3, 2, place Jussieu, 75251 Paris Cedex 05, France</nlm:aff></affiliation></author><author><name sortKey="Selwood, Lynne" sort="Selwood, Lynne" uniqKey="Selwood L" first="Lynne" last="Selwood">Lynne Selwood</name><affiliation><nlm:aff id="I7">Department of Zoology, Gate 12, University of Melbourne, Victoria. 3010, Australia</nlm:aff></affiliation></author><author><name sortKey="Ten Cate, Carel" sort="Ten Cate, Carel" uniqKey="Ten Cate C" first="Carel" last="Ten Cate">Carel Ten Cate</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation></author><author><name sortKey="Raynaud, Albert" sort="Raynaud, Albert" uniqKey="Raynaud A" first="Albert" last="Raynaud">Albert Raynaud</name><affiliation><nlm:aff id="I8">Formerly of Laboratoire Pasteur (Embryologie expérimentale), 20 rue des Moulins, 95110 Sannois, France</nlm:aff></affiliation></author><author><name sortKey="Osabutey, Casmile K" sort="Osabutey, Casmile K" uniqKey="Osabutey C" first="Casmile K" last="Osabutey">Casmile K. Osabutey</name><affiliation><nlm:aff id="I9">Department of Anatomy, St George's Hospital Medical School, Tooting, London SW17 0RE, UK</nlm:aff></affiliation></author><author><name sortKey="Richardson, Michael K" sort="Richardson, Michael K" uniqKey="Richardson M" first="Michael K" last="Richardson">Michael K. Richardson</name><affiliation><nlm:aff id="I1">Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</nlm:aff></affiliation></author></analytic><series><title level="j">BMC Evolutionary Biology</title><idno type="eISSN">1471-2148</idno><imprint><date when="2007">2007</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>Tetrapods exhibit great diversity in limb structures among species and also between forelimbs and hindlimbs within species, diversity which frequently correlates with locomotor modes and life history. We aim to examine the potential relation of changes in developmental timing (heterochrony) to the origin of limb morphological diversity in an explicit comparative and quantitative framework. In particular, we studied the relative time sequence of development of the forelimbs versus the hindlimbs in 138 embryos of 14 tetrapod species spanning a diverse taxonomic, ecomorphological and life-history breadth. Whole-mounts and histological sections were used to code the appearance of 10 developmental events comprising landmarks of development from the early bud stage to late chondrogenesis in the forelimb and the corresponding serial homologues in the hindlimb.</p></sec><sec><title>Results</title><p>An overall pattern of change across tetrapods can be discerned and appears to be relatively clade-specific. In the primitive condition, as seen in Chondrichthyes and Osteichthyes, the forelimb/pectoral fin develops earlier than the hindlimb/pelvic fin. This pattern is either retained or re-evolved in eulipotyphlan insectivores (= shrews, moles, hedgehogs, and solenodons) and taken to its extreme in marsupials. Although exceptions are known, the two anurans we examined reversed the pattern and displayed a significant advance in hindlimb development. All other species examined, including a bat with its greatly enlarged forelimbs modified as wings in the adult, showed near synchrony in the development of the fore and hindlimbs.</p></sec><sec><title>Conclusion</title><p>Major heterochronic changes in early limb development and chondrogenesis were absent within major clades except Lissamphibia, and their presence across vertebrate phylogeny are not easily correlated with adaptive phenomena related to morphological differences in the adult fore- and hindlimbs. The apparently conservative nature of this trait means that changes in chondrogenetic patterns may serve as useful phylogenetic characters at higher taxonomic levels in tetrapods. Our results highlight the more important role generally played by allometric heterochrony in this instance to shape adult morphology.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">BMC Evol Biol</journal-id><journal-title>BMC Evolutionary Biology</journal-title><issn pub-type="epub">1471-2148</issn><publisher><publisher-name>BioMed Central</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">17908305</article-id><article-id pub-id-type="pmc">2194785</article-id><article-id pub-id-type="publisher-id">1471-2148-7-182</article-id><article-id pub-id-type="doi">10.1186/1471-2148-7-182</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Forelimb-hindlimb developmental timing changes across tetrapod phylogeny</article-title></title-group><contrib-group><contrib id="A1" equal-contrib="yes" contrib-type="author"><name><surname>Bininda-Emonds</surname><given-names>Olaf RP</given-names></name><xref ref-type="aff" rid="I1">1</xref><xref ref-type="aff" rid="I2">2</xref><email>Olaf.Bininda@uni-jena.de</email></contrib><contrib id="A2" equal-contrib="yes" contrib-type="author"><name><surname>Jeffery</surname><given-names>Jonathan E</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>jon@isa.nl</email></contrib><contrib id="A3" equal-contrib="yes" contrib-type="author"><name><surname>Sánchez-Villagra</surname><given-names>Marcelo R</given-names></name><xref ref-type="aff" rid="I3">3</xref><email>m.sanchez@pim.uzh.ch</email></contrib><contrib id="A4" contrib-type="author"><name><surname>Hanken</surname><given-names>James</given-names></name><xref ref-type="aff" rid="I4">4</xref><email>hanken@oeb.harvard.edu</email></contrib><contrib id="A5" contrib-type="author"><name><surname>Colbert</surname><given-names>Matthew</given-names></name><xref ref-type="aff" rid="I5">5</xref><email>colbert@mail.utexas.edu</email></contrib><contrib id="A6" contrib-type="author"><name><surname>Pieau</surname><given-names>Claude</given-names></name><xref ref-type="aff" rid="I6">6</xref><email>m.k.richardson@biology.leidenuniv.nl</email></contrib><contrib id="A7" contrib-type="author"><name><surname>Selwood</surname><given-names>Lynne</given-names></name><xref ref-type="aff" rid="I7">7</xref><email>l.selwood@zoology.unimelb.edu.au</email></contrib><contrib id="A8" contrib-type="author"><name><surname>ten Cate</surname><given-names>Carel</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>c.j.ten.cate@biology.leidenuniv.nl</email></contrib><contrib id="A9" deceased="yes" contrib-type="author"><name><surname>Raynaud</surname><given-names>Albert</given-names></name><xref ref-type="aff" rid="I8">8</xref></contrib><contrib id="A10" contrib-type="author"><name><surname>Osabutey</surname><given-names>Casmile K</given-names></name><xref ref-type="aff" rid="I9">9</xref><email>m.k.richardson@biology.leidenuniv.nl</email></contrib><contrib id="A11" corresp="yes" contrib-type="author"><name><surname>Richardson</surname><given-names>Michael K</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>m.k.richardson@biology.leidenuniv.nl</email></contrib></contrib-group><aff id="I1"><label>1</label>Institute of Biology, University of Leiden, Kaiserstraat 63, 2311GP, Leiden, The Netherlands</aff><aff id="I2"><label>2</label>Institut für Spezielle Zoologie und Evolutionsbiologie mit Phyletischem Museum, Friedrich-Schiller-Universität Jena, Erbertstrasse 1, 07743 Jena, Germany</aff><aff id="I3"><label>3</label>Palaeontologisches Institut und Museum, Karl Schmid-Strasse 4, CH-8006 Zürich, Switzerland</aff><aff id="I4"><label>4</label>Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA</aff><aff id="I5"><label>5</label>Department of Geological Sciences, The University of Texas, Austin, TX 78712, USA</aff><aff id="I6"><label>6</label>Laboratoire de Biochimie du Développement, Institut Jacques Monod, CNRS et Université Paris 6 et 7, Tour 43-33, E3, 2, place Jussieu, 75251 Paris Cedex 05, France</aff><aff id="I7"><label>7</label>Department of Zoology, Gate 12, University of Melbourne, Victoria. 3010, Australia</aff><aff id="I8"><label>8</label>Formerly of Laboratoire Pasteur (Embryologie expérimentale), 20 rue des Moulins, 95110 Sannois, France</aff><aff id="I9"><label>9</label>Department of Anatomy, St George's Hospital Medical School, Tooting, London SW17 0RE, UK</aff><pub-date pub-type="collection"><year>2007</year></pub-date><pub-date pub-type="epub"><day>1</day><month>10</month><year>2007</year></pub-date><volume>7</volume><fpage>182</fpage><lpage>182</lpage><ext-link ext-link-type="uri" xlink:href="http://www.biomedcentral.com/1471-2148/7/182"></ext-link><history><date date-type="received"><day>26</day><month>2</month><year>2007</year></date><date date-type="accepted"><day>1</day><month>10</month><year>2007</year></date></history><permissions><copyright-statement>Copyright © 2007 Bininda-Emonds et al; licensee BioMed Central Ltd.</copyright-statement><copyright-year>2007</copyright-year><copyright-holder>Bininda-Emonds et al; licensee BioMed Central Ltd.</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0"></ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p><pmc-comment>
Bininda-Emonds
RP
Olaf
Olaf.Bininda@uni-jena.de
Forelimb-hindlimb developmental timing changes across tetrapod phylogeny
2007 BMC Evolutionary Biology 7(1): 182-. (2007) 1471-2148(2007)7:1<182> urn:ISSN:1471-2148
</license></permissions><abstract><sec><title>Background</title><p>Tetrapods exhibit great diversity in limb structures among species and also between forelimbs and hindlimbs within species, diversity which frequently correlates with locomotor modes and life history. We aim to examine the potential relation of changes in developmental timing (heterochrony) to the origin of limb morphological diversity in an explicit comparative and quantitative framework. In particular, we studied the relative time sequence of development of the forelimbs versus the hindlimbs in 138 embryos of 14 tetrapod species spanning a diverse taxonomic, ecomorphological and life-history breadth. Whole-mounts and histological sections were used to code the appearance of 10 developmental events comprising landmarks of development from the early bud stage to late chondrogenesis in the forelimb and the corresponding serial homologues in the hindlimb.</p></sec><sec><title>Results</title><p>An overall pattern of change across tetrapods can be discerned and appears to be relatively clade-specific. In the primitive condition, as seen in Chondrichthyes and Osteichthyes, the forelimb/pectoral fin develops earlier than the hindlimb/pelvic fin. This pattern is either retained or re-evolved in eulipotyphlan insectivores (= shrews, moles, hedgehogs, and solenodons) and taken to its extreme in marsupials. Although exceptions are known, the two anurans we examined reversed the pattern and displayed a significant advance in hindlimb development. All other species examined, including a bat with its greatly enlarged forelimbs modified as wings in the adult, showed near synchrony in the development of the fore and hindlimbs.</p></sec><sec><title>Conclusion</title><p>Major heterochronic changes in early limb development and chondrogenesis were absent within major clades except Lissamphibia, and their presence across vertebrate phylogeny are not easily correlated with adaptive phenomena related to morphological differences in the adult fore- and hindlimbs. The apparently conservative nature of this trait means that changes in chondrogenetic patterns may serve as useful phylogenetic characters at higher taxonomic levels in tetrapods. Our results highlight the more important role generally played by allometric heterochrony in this instance to shape adult morphology.</p></sec></abstract></article-meta></front><body><sec><title>Background</title><p>What evolutionary mechanisms are responsible for differences in the relative size of body parts among organisms? This basic question has long been confronted by biologists, for example, by J. S. Huxley, in his <italic>Problems of Relative Growth </italic>[<xref ref-type="bibr" rid="B1">1</xref>]. When considering the tetrapod limb, one might ask why the forelimbs are relatively larger or smaller than the hindlimbs in some species, and how these differences have arisen during evolution.</p><p>Tetrapods exhibit great diversity in limb structures among species and in differences between fore- and hindlimbs within species, which typically are correlated with locomotor modes and life history [<xref ref-type="bibr" rid="B2">2</xref>]. Among mammals, the relatively large wings of an adult bat exhibit a striking contrast in size and proportions to its legs, whereas the disparity in most other living eutherians (e.g. mice) is more modest. Kangaroos represent the opposite situation, having relatively massive hindlimbs. These differences are not restricted to mammals but characterize tetrapods as a whole, as evidenced when considering a bird or a frog or a turtle, or fossils such as <italic>Tyranosaurus rex</italic>, which has huge hindlimbs and tiny forelimbs.</p><p>A largely unanswered question is how these differences are reflected in the ontogenetic development of the limbs. Limbs are one of the best studied systems in both evolution and development [<xref ref-type="bibr" rid="B3">3</xref>] and display a sequence of well-defined temporal events, such as formation of the apical ectodermal ridge (AER) and the chondrification of skeletal elements. We examine here the extent to which features of early limb development, especially chondrogenesis, might be associated with obvious differences in forelimb and hindlimb size or function in the adult. We concentrate on heterochrony, the evolutionary change in developmental timing, a process which is thought to be important and common in evolution [<xref ref-type="bibr" rid="B4">4</xref>]. In particular, we examine the relative timing of developmental events during ontogeny across the phylogeny of the species examined (sequence heterochrony; sensu [<xref ref-type="bibr" rid="B5">5</xref>]).</p></sec><sec><title>Results</title><p>The average event-pair score (EPS; see Methods) was plotted for each species (Table <xref ref-type="table" rid="T1">1</xref>, Fig. <xref ref-type="fig" rid="F1">1</xref>). The two anurans (<italic>Xenopus</italic>, <italic>Eleutherodactylus</italic>) show average EPS scores significantly less than one, indicating that hindlimb development generally precedes that of the forelimb (noted by [<xref ref-type="bibr" rid="B6">6</xref>,<xref ref-type="bibr" rid="B7">7</xref>]). The two birds (<italic>Taeniopygia</italic>, <italic>Gallus</italic>) also tend to show an advance in hindlimb development – small differences between fore- and hindlimb timing can be detected visually (for example, in the figures of <italic>Gallus </italic>in [<xref ref-type="bibr" rid="B8">8</xref>]) – but are not significantly different from forelimb-hindlimb synchrony together with the remaining diapsids <italic>Lacerta </italic>and <italic>Emys</italic>. Among mammals, the marsupials (<italic>Trichosurus</italic>, <italic>Dasyurus </italic>and <italic>Sminthopsis</italic>) and eulipotyphlan insectivores (<italic>Erinaceus </italic>and <italic>Talpa</italic>) all show significant advances in forelimb development. The generally smaller forelimb advances among the remaining eutherian mammals were not significantly different from synchronous development.</p><table-wrap position="float" id="T1"><label>Table 1</label><caption><p>Statistics on the temporal distribution of developmental events</p></caption><table frame="hsides" rules="groups"><thead><tr><td align="left"><bold>Species (common name)</bold></td><td align="center"><bold><italic>N</italic></bold></td><td align="center"><bold>Avg. Stage</bold></td><td align="center"><bold><italic>EPS</italic></bold></td><td align="center"><bold>Student's <italic>t</italic></bold></td></tr></thead><tbody><tr><td align="left"><italic>Eleutherodactylus coqui </italic>(tree frog)</td><td align="center"><bold>12</bold></td><td align="center">3.091</td><td align="center">0.656 ± 0.110</td><td align="center"><italic>t</italic><sub>63 </sub>= -3.136 (<italic>P </italic>= 0.0026)</td></tr><tr><td align="left"><italic>Xenopus laevis </italic>(clawed toad)</td><td align="center"><bold>6</bold></td><td align="center">4.860</td><td align="center">0.625 ± 0.108</td><td align="center"><italic>t</italic><sub>63 </sub>= -3.473 (<italic>P </italic>= 0.0009)</td></tr><tr><td align="left"><italic>Emys orbicularis </italic>(pond turtle)</td><td align="center"><bold>10</bold></td><td align="center">3.333</td><td align="center">1.020 ± 0.093</td><td align="center"><italic>t</italic><sub>99 </sub>= 0.215 (<italic>P </italic>= 0.8305)</td></tr><tr><td align="left"><italic>Lacerta viridis </italic>(wall lizard)</td><td align="center"><bold>12</bold></td><td align="center">2.857</td><td align="center">1.020 ± 0.093</td><td align="center"><italic>t</italic><sub>99 </sub>= 0.215 (<italic>P </italic>= 0.8305)</td></tr><tr><td align="left"><italic>Gallus gallus </italic>(chicken)</td><td align="center"><bold>10</bold></td><td align="center">2.188</td><td align="center">0.875 ± 0.121</td><td align="center"><italic>t</italic><sub>63 </sub>= -1.033 (<italic>P </italic>= 0.3054)</td></tr><tr><td align="left"><italic>Taeniopygia guttata </italic>(zebra finch)</td><td align="center"><bold>7</bold></td><td align="center">3.091</td><td align="center">0.922 ± 0.112</td><td align="center"><italic>t</italic><sub>63 </sub>= -0.697 (<italic>P </italic>= 0.4882)</td></tr><tr><td align="left"><italic>Trichosurus vulpecula </italic>(brushtail possum)</td><td align="center"><bold>15</bold></td><td align="center">2.500</td><td align="center">1.640 ± 0.076</td><td align="center"><italic>t</italic><sub>99 </sub>= 8.432 (<italic>P </italic>< 0.0001)</td></tr><tr><td align="left"><italic>Sminthopsis macroura </italic>(stripe-faced dunnart)</td><td align="center"><bold>5</bold></td><td align="center">8.000</td><td align="center">1.730 ± 0.060</td><td align="center"><italic>t</italic><sub>99 </sub>= 12.155 (<italic>P </italic>< 0.0001)</td></tr><tr><td align="left"><italic>Dasyurus viverrinus </italic>(marsupial cat)</td><td align="center"><bold>11</bold></td><td align="center">3.077</td><td align="center">1.850 ± 0.048</td><td align="center"><italic>t</italic><sub>99 </sub>= 17.732 (<italic>P </italic>< 0.0001)</td></tr><tr><td align="left"><italic>Erinaceus europaeus </italic>(hedgehog)</td><td align="center"><bold>10</bold></td><td align="center">3.333</td><td align="center">1.200 ± 0.094</td><td align="center"><italic>t</italic><sub>99 </sub>= 2.121 (<italic>P </italic>= 0.0364)</td></tr><tr><td align="left"><italic>Talpa europea </italic>(mole)</td><td align="center"><bold>10</bold></td><td align="center">3.333</td><td align="center">1.230 ± 0.089</td><td align="center"><italic>t</italic><sub>99 </sub>= 2.596 (<italic>P </italic>= 0.0109)</td></tr><tr><td align="left"><italic>Mus musculus </italic>(mouse)</td><td align="center"><bold>12</bold></td><td align="center">2.857</td><td align="center">1.090 ± 0.096</td><td align="center"><italic>t</italic><sub>99 </sub>= 0.933 (<italic>P </italic>= 0.3533)</td></tr><tr><td align="left"><italic>Rousettus amplexicaudatus </italic>(fruitbat)</td><td align="center"><bold>10</bold></td><td align="center">3.800</td><td align="center">1.000 ± 0.101</td><td align="center"><italic>t</italic><sub>89 </sub>= 0.000 (<italic>P </italic>= 1.000)</td></tr><tr><td align="left"><italic>Cynocephalus variegatus </italic>(flying lemur)</td><td align="center"><bold>8</bold></td><td align="center">3.333</td><td align="center">1.080 ± 0.088</td><td align="center"><italic>t</italic><sub>99 </sub>= 0.905 (<italic>P </italic>= 0.3677)</td></tr></tbody></table><table-wrap-foot><p>The event-pair score (EPS; presented as average ± SE) may range from 2 (forelimb advanced over hindlimb) to 0 (hindlimb advanced over forelimb). Two-tailed Student's <italic>t</italic>-tests were used to determine if the EPS was significantly different from 1. <italic>N </italic>is the number of stages of limb development identified and Avg. Stage is the mean number of events that occurred at each stage.</p></table-wrap-foot></table-wrap><fig position="float" id="F1"><label>Figure 1</label><caption><p>Average event-pair scores (EPSs) plotted on a phylogeny of the taxa examined, with visual examples of forelimb (FL) and hindlimb (HL) across the tree. Plot symbols in blue and green are significantly less than and greater than one, respectively; forelimb-hindlimb synchrony, in red. The tree is derived from references 33 and 34.</p></caption><graphic xlink:href="1471-2148-7-182-1"></graphic></fig><p>An analysis of variance in combination with Fisher's PLSD test detected four major clades among the tetrapod species we examined (<italic>F</italic><sub>3,1242 </sub>= 66.418, <italic>P </italic>< 0.0001):</p><p>1. anuran amphibians: strong, significant hindlimb acceleration with an average EPS of 0.641 ± 0.076 (SE);</p><p>2. diapsids (lizards, turtles, and birds): slight, but insignificant hindlimb acceleration with an average EPS of 0.973 ± 0.051;</p><p>3. eutherian mammals: slight, but insignificant forelimb acceleration with an average EPS of 1.122 ± 0.042;</p><p>4. marsupial mammals: strong, significant forelimb acceleration with an average EPS of 1.740 ± 0.036.</p></sec><sec><title>Discussion</title><p>The relative timing of fore- and hindlimb development is labile in evolution, but with the observed pattern of change in timing showing a strong phylogenetic component. Different clades (anurans, diapsids, eutherians and marsupials) each have evolved characteristic timing relationships (see also Figure <xref ref-type="fig" rid="F2">2</xref>) that show no apparent correlation to the diverse lifestyles and adult morphologies of the species within each clade. The relative conservation of timing relationships within clades in the face of disparate adaptive needs is particularly striking among eutherians, which included a flying species (<italic>Rousettus</italic>), a glider (<italic>Cynocephalus</italic>), and a terrestrial species (<italic>Mus</italic>). Although the eulipotyphlan insectivores <italic>Erinaceus </italic>and <italic>Talpa </italic>do show a significant forelimb advance within and with respect to other eutherian mammals, this pattern is also consistent for the clade despite the different locomotory modes of the exemplars (terrestrial and fossorial, respectively). In short, the strong selection for modification of the adult limb morphology in eutherians did not produce correlated changes in the relative timing of forelimb-hindlimb development.</p><fig position="float" id="F2"><label>Figure 2</label><caption><p>Reconstruction of the relative timing of forelimb and hindlimb development in tetrapods. Branches in blue and green show cases of significant hindlimb versus forelimb advances, respectively. Branches in red indicate synchrony and branches in black are equivocal according to the parsimony reconstruction. The tree is derived from references 33 and 34.</p></caption><graphic xlink:href="1471-2148-7-182-2"></graphic></fig><p>The only exceptions to the general pattern of clade-dependent conservation across tetrapods that we are aware of occur in lissamphibians. In anurans, the limbs develop approximately in synchrony in <italic>Rana temporaria </italic>[<xref ref-type="bibr" rid="B9">9</xref>] in contrast to the hindlimb acceleration found in the two species we examined. Among other lissamphibians, it is known that in some urodeles such as the smooth newt <italic>Triturus vulgaris</italic>, the forelimb is so accelerated relative to the hindlimb that it is chondrified before the bud of the latter has even appeared [<xref ref-type="bibr" rid="B10">10</xref>]. Forelimb advanced over the hindlimb also characterizes the Iberian ribbed newt <italic>Pleurodeles watl </italic>[<xref ref-type="bibr" rid="B11">11</xref>]. In other urodeles, such as the Siberian newt <italic>Salamandrella keyserlingii </italic>[<xref ref-type="bibr" rid="B12">12</xref>] and the clawed salamander <italic>Onychodactylus japonica </italic>[<xref ref-type="bibr" rid="B13">13</xref>], the forelimb is only marginally advanced if at all or, as in the Mexican plethodontid <italic>Chiropterotriton magnipes</italic>, the two limbs reportedly develop more or less simultaneously [<xref ref-type="bibr" rid="B14">14</xref>]. Increased species sampling may reveal yet additional variation within Lissamphibia.</p><p>Altogether, there was little evidence that adaptations of the adult tetrapod limb were associated with fore-/hindlimb sequence heterochrony during chondrogenesis. Instead, it appears that post-chondrogenic differences in growth rate (i.e., allometric heterochrony) play a more deciding role in shaping the final adult morphology of the tetrapod limb. A cogent example are marsupials, which often display a much larger hindlimb in adults despite the extreme acceleration of forelimb development in embryos. Similarly, the bat actually displayed the least degree of forelimb acceleration among the eutherians studied, despite the forelimbs being greatly enlarged and modified as wings in the adult. This morphology appears to derive from allometric heterochrony instead: the initially conserved pattern of chondrogenesis is followed by accelerated chondrocyte proliferation and differentiation, with increased <italic>Bmp2 </italic>expression and Bmp signalling [<xref ref-type="bibr" rid="B15">15</xref>]. A similar phenomenon of allometric and not sequence heterochrony was hypothesized by Jeffery et al. [<xref ref-type="bibr" rid="B16">16</xref>] to account for eye development in the spectral tarsier (<italic>Tarsius spectrum</italic>), a nocturnal primate with the largest relative eye-size among mammals.</p><p>An important question, therefore, is what is driving the changes in the early pattern of chondrogenesis among the major tetrapod clades, especially in light of the apparent conservation of this trait within most of them. Similar developmental pathways are responsible for the patterning and growth of fore- and hindlimbs, and covariation between both has been recorded statistically at different levels of the phylogenetic hierarchy in adults [<xref ref-type="bibr" rid="B17">17</xref>]. Yet, our study shows that heterochronic changes and dissociation have still occurred across major tetrapod clades and within lissamphibians to occasionally override the common mechanisms underlying limb development.</p><p>One possible explanation for the inferred transformations is that the different patterns are directly adaptive for the embryo. This has been hypothesized for marsupials and monotremes, where the greatly accelerated forelimb development has been linked to the necessity for the embryo to climb to the mother's marsupium to attach to a teat for further development [<xref ref-type="bibr" rid="B5">5</xref>]. Similarly, marsupials show another one of the few, clear instances of sequence heterochrony in mammals, with many cranial structures associated with feeding in the pouch also showing advanced development [<xref ref-type="bibr" rid="B5">5</xref>,<xref ref-type="bibr" rid="B18">18</xref>,<xref ref-type="bibr" rid="B19">19</xref>]. Similar adaptive explanations are lacking for the remaining species, however. This is particularly true for the two anurans examined here (<italic>Eleutherodactylus</italic>, <italic>Xenopus</italic>), which show a conserved pattern despite their very different developmental modes (direct versus indirect, respectively). Altogether, adaptive explanations seem difficult to postulate in general and for the amniotes in particular, the embryos of which develop in the protected environment of the cleidoic egg and so might be evolutionarily 'privileged' (sensu [<xref ref-type="bibr" rid="B20">20</xref>]) and shielded from diversifying selection.</p><p>An alternative, but not mutually exclusive, explanation is the presence of developmental 'constraints' [<xref ref-type="bibr" rid="B21">21</xref>] or that the overall pattern is the 'by-product' of other developmental processes. Although our findings are consistent with the existence of such constraints, they in no way can be taken as evidence of their existence.</p><p>We would add that the general pattern of fore- and hindlimb developmental timing we present based on 10 developmental landmarks belies its actual complexity. In <italic>Dasyurus</italic>, for example, although the forelimb buds appear before those of the hindlimb, a clear hindlimb bud is present throughout most of forelimb development. However, chondrogenesis does not start in the hindlimb buds until forelimb development is nearly complete. The initial timing difference between the appearance of fore- and hindlimb buds correlates with the strong craniocaudal developmental gradient observed at early stages of development [<xref ref-type="bibr" rid="B22">22</xref>]. However, the failure of the hindlimb bud to progress after its initial formation (a period of developmental 'dormancy'), is likely to be caused by more local factors, effectively maintaining a viable limb-bud whilst temporarily suspending outgrowth.</p></sec><sec><title>Conclusion</title><p>We find that the relative timing of forelimb versus hindlimb development varies widely between major vertebrate clades. However, such forelimb-hindlimb sequence heterochronies are largely absent within major clades, the Lissamphibia forming a notable exception. The sequence differences that we did note between fore- and hindlimbs were not easy to explain in terms of morphological differences in the adult fore- and hindlimbs. Rather, the latter were more likely explained by allometric growth differences. The apparently conservative nature of forelimb versus hindlimb timing may mean that of skeletal chondrogenesis sequences could provide useful phylogenetic characters at higher taxonomic levels in tetrapods.</p><p>Our data, and those summarized in Rabl [<xref ref-type="bibr" rid="B23">23</xref>] and Richardson [<xref ref-type="bibr" rid="B24">24</xref>] allow an initial attempt to reconstruct the evolution of forelimb-hindlimb heterochrony across tetrapods (Figure <xref ref-type="fig" rid="F2">2</xref>). The primitive tetrapod condition appears to be for the forelimb to be advanced over the hindlimb (see also [<xref ref-type="bibr" rid="B25">25</xref>]). This condition characterizes the primitive condition for the homologous structures (the pectoral and pelvic fins, although many tetrapod autopodial structures are most likely absent in fishes [<xref ref-type="bibr" rid="B26">26</xref>]) in Chondrichthyes and Osteichthyes [<xref ref-type="bibr" rid="B24">24</xref>]. Thereafter, the evolution of this trait is equivocal (as indicated by the black branches in Figure <xref ref-type="fig" rid="F2">2</xref>), with two equally parsimonious solutions. One solution is for the forelimb advance to be retained ancestrally throughout tetrapods, with the individual groups (anurans, diapsids, marsupials, <italic>Rousettus</italic>, and <italic>Mus </italic>+ <italic>Cynocephalus</italic>) independently deviating from this pattern. The other solution is for a hindlimb advance to be a shared derived feature (synapomorphy) of amniotes, with marsupials and eulipotyphlan insectivores independently regaining the primitive tetrapod hindlimb advance.</p><p>Additional data will help clarify this picture, both by testing the reality of the apparent clade-specificity of forelimb-hindlimb heterochrony and by hopefully resolving outstanding regions of uncertainty. Key among the latter is within urodeles, where there is evidence that the pattern we present might not hold in unsampled species [<xref ref-type="bibr" rid="B10">10</xref>-<xref ref-type="bibr" rid="B14">14</xref>].</p></sec><sec sec-type="methods"><title>Methods</title><p>We analysed developmental sequences in 138 embryos of 14 species, spanning a diverse taxonomic, ecomorphological and life-history breadth. Specimens were obtained from the Zeilstra and M.K. Richardson collections, Institute of Biology, University of Leiden; Hubrecht Laboratory, Netherlands Institute for Developmental Biology and Naturalis Museum, Leiden. We used whole-mounts prepared using standard protocols and viewed through an orange (G) filter to improve the contrast. Some histological sections were made to ensure that differences in staining time did not affect the scoring of skeletal elements. All had been collected in accordance with local ethical rules. Work on <italic>Eleutherodactylus </italic>was approved by the Harvard University, Faculty of Arts & Sciences, Standing Committee on the use of Animals in Research and Teaching, animal experimentation protocol (AEP) 99-09.</p><p>A total of 20 events was scored (Table <xref ref-type="table" rid="T2">2</xref>), providing landmarks of development from the early bud stage to late chondrogenic events. All specimens were scored by JEJ. As a control, MKR independently scored a subset of several species; results were identical. The score '0' was assigned if an event had not yet occurred, and '2' if it had occurred. The score '1' was used to indicate an intermediate phase, such as if a cartilage element was stained but lacked distinct boundaries (i.e., it was a diffuse patch that graded imperceptibly into the surrounding tissue). We assumed the homology of the events, both amongst species (primary homology), and between the fore- and hindlimbs of individuals (serial homology).</p><table-wrap position="float" id="T2"><label>Table 2</label><caption><p>Limb developmental events scored in this analysis</p></caption><table frame="hsides" rules="groups"><thead><tr><td align="center"><bold><italic>Forelimb event</italic></bold></td><td align="center"><bold><italic>Hindlimb event</italic></bold></td></tr></thead><tbody><tr><td align="center" colspan="2"><italic>External Form</italic></td></tr><tr><td colspan="2"><hr></hr></td></tr><tr><td align="left">A. bud first distinct</td><td align="left">K. bud first distinct</td></tr><tr><td align="left">B. AER appears</td><td align="left">L. AER appears</td></tr><tr><td align="left">C. digital plate crenation (fossae separating digits dorsally)</td><td align="left">M. digital plate crenation (fossae separating digits dorsally)</td></tr><tr><td colspan="2"><hr></hr></td></tr><tr><td align="center" colspan="2"><italic>Chondrogenesis</italic></td></tr><tr><td colspan="2"><hr></hr></td></tr><tr><td align="left">D. humerus appears</td><td align="left">N. femur appears</td></tr><tr><td align="left">E. ulna appears</td><td align="left">O. fibula appears</td></tr><tr><td align="left">F. proximal carpal (ulnare) appears</td><td align="left">P. proximal tarsal (fibulare) appears</td></tr><tr><td align="left">G. carpal distal to ulnare appears</td><td align="left">Q. tarsal distal to fibulare appears</td></tr><tr><td align="left">H. metacarpal appears</td><td align="left">R. metatarsal appears</td></tr><tr><td align="left">I. proximal phalanx appears</td><td align="left">S. proximal phalanx appears</td></tr><tr><td align="left">J. distal phalanx appears</td><td align="left">T. distal phalanx appears</td></tr></tbody></table><table-wrap-foot><p>Elements in the same horizontal row in the hand and foot are considered serially homologous for the purposes of this study.</p></table-wrap-foot></table-wrap><p>Stylopodal and zeugopodal elements have clear homologues between the fore and hindlimbs (humerus/femur, radius/tibia and ulna/fibula). A basipodial element (ulnare/fibulare) also could be identified in most species. The total number of phalanges on a particular digit, however, varies amongst species. We therefore chose to record only the most proximal and distal phalanges, which provide proximal and distal landmarks for chondrogenesis in a given digit. The AER is absent in one of the anuran species considered here (<italic>Eleutherodactylus coqui</italic>; [<xref ref-type="bibr" rid="B7">7</xref>]), and very reduced in the other (<italic>Xenopus laevis</italic>; [<xref ref-type="bibr" rid="B27">27</xref>]).</p><p>Autopodials of the species studied vary in the number and pattern of prechondrogenic primordia, the pattern of fusion or regression during development, and in adult morphology (e.g., the numbers of digits and phalanges). We resolved these difficulties by looking at common (possibly plesiomorphic) patterns of development. In the forelimb, the digit adjacent to the ulna and ulnare is the first to develop [<xref ref-type="bibr" rid="B28">28</xref>,<xref ref-type="bibr" rid="B29">29</xref>]. We therefore selected this digit (and its associated metacarpal) as a proxy for overall digital development. A similar pattern is seen in the hindlimb with respect to the fibula and fibulare. In pentadactyl amniotes this digit invariably is digit IV.</p><sec><title>Reconstructing the developmental sequence</title><p>The embryonic age was unknown for most specimens. Even so, the very existence of intraspecific heterochrony means that absolute age usually cannot be considered to be a reliable criterion for ordering specimens in a developmental sequence [<xref ref-type="bibr" rid="B30">30</xref>]. We therefore used the parsimony-based 'Ontogenetic Sequence Analysis' (OSA [<xref ref-type="bibr" rid="B31">31</xref>]) on the limb character distribution amongst the specimens to find the most parsimonious developmental sequence for each species. OSA provides a rigorous framework for optimizing variations (polymorphisms) in the developmental sequence of a species to yield a single, consensus sequence. It relies on two assumed characteristics of development: (1) progressiveness – for any set of events, it is possible to conceive an early embryo in which none of the events has occurred, and a late embryo in which all the events have occurred; and (2) irreversibility – the same event cannot occur twice to the same organ.</p><p>Data for each species were analysed using the <italic>TAXEQ2 </italic>program [<xref ref-type="bibr" rid="B32">32</xref>], to identify specimens having actual or potentially equivalent scores (when missing data are taken into account). Such embryos were excluded from the analysis to reduce the computational time for OSA without the loss of any novel information.</p></sec><sec><title>Intraspecific developmental rates</title><p>Comparisons of the relative rates of development between fore- and hindlimbs within each species were made using the event-pair method. This method encodes the relative timing between any two developmental events, with 0 indicating that event A occurred before event B, 1 indicating that both occurred simultaneously, and 2 indicating that event B occurred first. To highlight differential rates of development between the limbs without regard to any sequence changes within each limb we compared the 100 non-redundant event-pairs involving each homologous forelimb and hindlimb event (for a data set of <italic>N </italic>serially homologous events = <italic>N</italic><sup>2</sup>; <italic>N </italic>= 10 here). All event pairs were scored from the standard 'perspective' of hindlimb-event vs. forelimb-event (i.e., rather than forelimb event vs. hindlimb event; cf. [<xref ref-type="bibr" rid="B18">18</xref>]).</p><p>The average event-pair score (EPS; i.e. the sum of all event-pair scores divided by the number of event-pairs) was analyzed to describe the overall timing of fore- and hindlimb development in each species. If fore- and hindlimbs developed synchronously, there would be 10 'simultaneous' event-pair scores (one for every pair of serially homologous events, each scoring 1) and 45 scores each of 'before' (scoring 0) and 'after' (scoring 2). Thus, the average value of EPS would be (10 × 1 + 45 × 0 + 45 × 2)/100 = 1. If the forelimb moved late relative to the hindlimb, the ratio of 'before' to 'after' scores would decrease, moving the average EPScloser to zero. Conversely, if the forelimb moved early relative to the hindlimb, the ratio of 'before' to 'after' scores would increase, moving the average EPS closer to two. The average EPS therefore provides an indicator of the relative timing of fore- and hindlimb development.</p><p>It is not clear precisely how the average EPS is affected by lack of resolution in a developmental sequence, but, in general, an increased number of simultaneous scores will tend to push the value towards one. Any lack of resolution is more likely to affect comparisons of events within the forelimb or the hindlimb, rather than the homologous events between the limbs, especially when the two sets of limbs develop asynchronously.</p></sec></sec><sec><title>Competing interests</title><p>The author(s) declares that there are no competing interests.</p></sec><sec><title>Authors' contributions</title><p>JEJ and MKR collected the data, JEJ, ORPB-E and MKR carried out the analyses, MRS-V, ORPB-E, JH and MKR wrote the manuscript, MC advised on the analyses, JH, CP, LS, CtC, AR and CKO provided embryonic materials for the study and participated in discussions, and MKR conceived of the project. All authors read and approved the final manuscript.</p></sec></body><back><ack><sec><title>Acknowledgements</title><p>This paper is dedicated to the memories of A. Raynaud and H. Dudart. We thank K. Noorlander, M. de Bakker, Y. Bland and P. Bagley for their histological expertise and the late H. Dudart for his help with the zebra finches. Two anonymous reviewers and JR Hinchliffe made very useful suggestions that greatly helped to improve the manuscript. JEJ was supported by the Leverhulme Trust, and by the van der Leeuw funds. LS was supported by the Australian Research Council and the Ministry of Agriculture and Forestry, New Zealand. JH was supported by NSF. ORPB-E was supported by the van der Leeuw Fonds and a DFG Heisenberg Scholarship (BI 825/2-1). 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