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>Introduction to: Snakes from the Cenozoic of Europe – towards a macroevolutionary and palaeobiogeographic synthesis</title
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>Introduction to: Snakes from the Cenozoic of Europe</title
><author
role="aut"
><name
>Georgios L. GEORGALIS</name
><affiliation
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><name
>Hussam ZAHER</name
><affiliation
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></affiliation
><idno
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>0000-0002-6994-489X</idno
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><author
role="aut"
><name
>Michel LAURIN</name
><affiliation
><ref
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></ref
></affiliation
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>0000-0003-2974-9835</idno
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>2026-02-05T13:54:00</date
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>20/12/2024</date
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>04/02/2025</date
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>45-49</dim
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>19/02/2025</date
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>24</idno
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>19/02/2025</date
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>Introduction to: Snakes from the Cenozoic of Europe – towards a macroevolutionary and palaeobiogeographic synthesis</titlePart
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n="1"
style="txt_auteurs"
><ref
target="https://sciencepress.mnhn.fr/fr/auteurs/georgios-l-georgalis"
>Georgios L. GEORGALIS</ref
></byline
><byline
n="2"
style="txt_auteurs"
><affiliation
xml:id="aff01"
>Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Sławkowska 17, 31-016 Kraków (Poland) </affiliation
><ref
target="mailto:georgalis@isez.pan.krakow.pl"
><affiliation
xml:id="aff02"
>georgalis@isez.pan.krakow.pl</affiliation
></ref
><affiliation
xml:id="aff03"
> (corresponding author)</affiliation
></byline
><byline
n="3"
style="txt_auteurs"
><ref
target="https://sciencepress.mnhn.fr/fr/auteurs/hussam-zaher"
>Hussam ZAHER</ref
></byline
><byline
n="4"
style="txt_auteurs"
><affiliation
xml:id="aff04"
>Museu de Zoologia, Universidade de São Paulo, Avenida Nazaré 481, Ipiranga 04263-000, São Paulo, SP (Brazil)</affiliation
></byline
><byline
n="5"
style="txt_auteurs"
><ref
target="https://sciencepress.mnhn.fr/fr/auteurs/michel-laurin"
>Michel LAURIN</ref
></byline
><byline
n="6"
style="txt_auteurs"
><affiliation
xml:id="aff06"
>Centre de Recherches en paléontologie – Paris (CR2P), Centre national de la Recherche scientifique (CNRS), Muséum national d’Histoire naturelle (MNHN), Sorbonne Université, Département Origines &amp; Évolution, CP 38, 57 rue Cuvier, F-75231Paris cedex 05 (France)</affiliation
></byline
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type="chapitre"
xml:id="mainDiv"
><p
style="txt_Normal"
>Georgalis G. L., Zaher H. &amp; Laurin M. 2025. — Introduction to: Snakes from the Cenozoic of Europe – towards a macroevolutionary and palaeobiogeographic synthesis, <hi
rend="italic"
style="typo_Italique"
>in</hi
> ­Georgalis G. L., Zaher H. &amp; Laurin M. (eds), Snakes from the Cenozoic of Europe – towards a macroevolutionary and palaeobiogeographic synthesis. <hi
rend="italic"
style="typo_Italique"
>Comptes Rendus Palevol</hi
> 24 (3): 45-49. <ref
target="https://doi.org/10.5852/cr-palevol2025v24a3"
><hi
rend="underline"
style="typo_souligne"
>https://doi.org/10.5852/cr-palevol2025v24a3</hi
></ref
></p
><p
style="txt_Normal"
>Snakes have long been important components of most European ecosystems. This is not readily obvious to herpetologists given that the modest extant taxonomic richness represents simply a glimpse of their astonishing abundance in Europe during much of the Cenozoic. Indeed, the fossil record documents a high taxonomic diversity of snakes, which included a plethora of distinct shapes, sizes, feeding and reproductive adaptations, ecological strategies, and locomotion (<ref
target="#_idTextAnchor029"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rage 1984</hi
></ref
>; <ref
target="#_idTextAnchor016"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 2022</hi
></ref
>; <ref
target="#_idTextAnchor036"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Georgalis 2022)</hi
></ref
>. Interestingly (as of February 2025), as many as 162 extinct species have been established from the Cenozoic of Europe; these 162 species have been assigned to 92 different genera, among which 56 genera are extinct and established upon European fossil material, 10 genera are extinct and have originally established upon fossil material from other continents, and 26 represent extant genera (GLG, unpublished data). This high diversity included both early representatives of extant clades that now inhabit the continent, such as erycids, colubrids, natricids, and viperids (<ref
target="#_idTextAnchor041"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar 1984</hi
></ref
>, <ref
target="#_idTextAnchor042"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1991a</hi
></ref
>, <ref
target="#_idTextAnchor043"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>b</hi
></ref
>; <ref
target="#_idTextAnchor016"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 2022)</hi
></ref
>, giant forms of extant clades of the continent (<ref
target="#_idTextAnchor009"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2016)</hi
></ref
>, as well as taxa that are now absent from Europe, such as pythonids and elapids (<ref
target="#_idTextAnchor029"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rage 1984</hi
></ref
>; <ref
target="#_idTextAnchor042"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar 1991a</hi
></ref
>, <ref
target="#_idTextAnchor043"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>b</hi
></ref
>; <ref
target="#_idTextAnchor047"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar &amp; Rage 2003</hi
></ref
>; <ref
target="#_idTextAnchor049"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Zaher &amp; Smith 2020</hi
></ref
>; <ref
target="#_idTextAnchor016"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 2022)</hi
></ref
>, but also a parade of unique, bizarre, and now extinct clades, such as palaeophiids, russellophiids, and anomalophiids (<ref
target="#_idTextAnchor028"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rage 1983</hi
></ref
>, <ref
target="#_idTextAnchor029"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1984</hi
></ref
>; <ref
target="#_idTextAnchor010"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2020</hi
></ref
>; <ref
target="#_idTextAnchor036"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Georgalis 2022</hi
></ref
>; <ref
target="#_idTextAnchor051"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Fig. 1</hi
></ref
>).</p
><p
style="txt_Normal"
>Fossil snake remains from the European Cenozoic consist primarily of isolated vertebrae (<ref
target="#_idTextAnchor029"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rage 1984</hi
></ref
>; <ref
target="#_idTextAnchor041"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar 1984</hi
></ref
>, <ref
target="#_idTextAnchor042"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1991a</hi
></ref
>, <ref
target="#_idTextAnchor043"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>b</hi
></ref
>; <ref
target="#_idTextAnchor048"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Venczel 2000</hi
></ref
>; <ref
target="#_idTextAnchor047"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar &amp; Rage 2003</hi
></ref
>; <ref
target="#_idTextAnchor016"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 2022</hi
></ref
>; <ref
target="#_idTextAnchor036"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Georgalis 2022</hi
></ref
>; <ref
target="#_idTextAnchor051"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Fig. 1</hi
></ref
>). Articulated vertebrae and cranial remains are less common (e.g. <ref
target="#_idTextAnchor023"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Owen 1850</hi
></ref
>; <ref
target="#_idTextAnchor040"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szunyoghy 1932</hi
></ref
>; <ref
target="#_idTextAnchor012"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Hoffstetter 1939</hi
></ref
>; <ref
target="#_idTextAnchor041"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar 1984</hi
></ref
>; <ref
target="#_idTextAnchor015"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 1999</hi
></ref
>; <ref
target="#_idTextAnchor048"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Venczel 2000</hi
></ref
>; <ref
target="#_idTextAnchor047"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar &amp; Rage 2003</hi
></ref
>; <ref
target="#_idTextAnchor011"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2021</hi
></ref
>; <ref
target="#_idTextAnchor007"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis &amp; Scheyer 2022</hi
></ref
>; <ref
target="#_idTextAnchor003"
><hi
rend="underline"
style="typo_souligne"
>Čerňanský 2024</hi
></ref
>; <ref
target="#_idTextAnchor051"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Fig. 1</hi
></ref
>), while complete skeletons are exceptionally rare and typically limited to a few Fossillagerstätte localities (<ref
target="#_idTextAnchor021"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Meyer 1845</hi
></ref
>; <ref
target="#_idTextAnchor020"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Massalongo 1859</hi
></ref
>; <ref
target="#_idTextAnchor017"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Janensch 1906</hi
></ref
>; <ref
target="#_idTextAnchor019"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Kuhn 1939</hi
></ref
>; <ref
target="#_idTextAnchor044"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar 1992</hi
></ref
>; <ref
target="#_idTextAnchor045"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar &amp; Böhme 1996</hi
></ref
>; <ref
target="#_idTextAnchor001"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Baszio 2004</hi
></ref
>; <ref
target="#_idTextAnchor037"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Scanferla 2016</hi
></ref
>, <ref
target="#_idTextAnchor038"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>2021</hi
></ref
>, <ref
target="#_idTextAnchor039"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>2022</hi
></ref
>; <ref
target="#_idTextAnchor034"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Scanferla &amp; Smith 2020</hi
></ref
>; <ref
target="#_idTextAnchor049"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Zaher &amp; Smith 2020</hi
></ref
>; <ref
target="#_idTextAnchor011"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2021</hi
></ref
>; <ref
target="#_idTextAnchor035"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Seghetti et al. 2022</hi
></ref
>; <ref
target="#_idTextAnchor025"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Palci et al. 2024</hi
></ref
>; <ref
target="#_idTextAnchor051"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Fig. 1</hi
></ref
>). Remarkably, even mummified portions of snake bodies have been recovered in exceptional cases (<ref
target="#_idTextAnchor005"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Filhol 1877</hi
></ref
>; <ref
target="#_idTextAnchor032"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rochebrune 1884</hi
></ref
>; <ref
target="#_idTextAnchor011"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2021</hi
></ref
>; <ref
target="#_idTextAnchor051"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Fig. 1</hi
></ref
>)! Notably, the beautifully preserved skeletons from the Fossillagerstätte localities of Messel and Geiseltal in Germany have provided and continue to provide critical insight into the cranial anatomy and intracolumnar variation of multiple extinct snake taxa (<ref
target="#_idTextAnchor019"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Kuhn 1939</hi
></ref
>; <ref
target="#_idTextAnchor001"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Baszio 2004</hi
></ref
>; <ref
target="#_idTextAnchor034"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Scanferla &amp; Smith 2020</hi
></ref
>; <ref
target="#_idTextAnchor049"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Zaher &amp; Smith 2020</hi
></ref
>; <ref
target="#_idTextAnchor038"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Scanferla 2021</hi
></ref
>, <ref
target="#_idTextAnchor039"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>2022</hi
></ref
>; <ref
target="#_idTextAnchor011"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2021</hi
></ref
>; <ref
target="#_idTextAnchor025"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Palci et al. 2024</hi
></ref
>; <ref
target="#_idTextAnchor051"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Fig. 1</hi
></ref
>). Additionally, these fossils offer valuable information on palaeoecology and trophic interactions (e.g. <ref
target="#_idTextAnchor037"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Scanferla 2016)</hi
></ref
>.</p
><p
style="txt_Normal"
>The European Cenozoic fossil record of snakes dates back to the Paleocene and encompasses a wide geographic distribution. As such, it provides valuable insights into major climatic events, dispersals, faunal turnovers, and extinctions that shaped the European Cenozoic faunas, ultimately leading to the emergence of extant taxa. Such prominent events that affected European snake faunas include the high temperatures observed during the Paleocene-Eocene Thermal Maximum (PETM) and the Early Eocene Climatic Optimum (EECO), the cooling that triggered the “Grande Coupure” at the Eocene-Oligocene boundary, or the distinct palaeogeographic settings that arose during the formation of the “<hi
rend="italic"
style="typo_Italique"
>Gomphotherium </hi
>Landbridge” during the Early Miocene, and the Messinian Salinity Crisis during the Miocene-Pliocene boundary (<ref
target="#_idTextAnchor047"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar &amp; Rage 2003</hi
></ref
>; <ref
target="#_idTextAnchor030"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rage 2013</hi
></ref
>; <ref
target="#_idTextAnchor050"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Zaher et al. 2019</hi
></ref
>; <ref
target="#_idTextAnchor011"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis et al. 2021</hi
></ref
>; <ref
target="#_idTextAnchor016"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 2022</hi
></ref
>; <ref
target="#_idTextAnchor008"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Georgalis &amp; Szyndlar 2022</hi
></ref
>; <ref
target="#_idTextAnchor036"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Georgalis 2022)</hi
></ref
>. However, significant gaps remain from both a stratigraphic and a geographic point of view. Indeed, stratigraphically speaking, some geological epochs, such as the Paleocene and the Oligocene, are underrepresented, compared to other epochs, in the European snake fossil record (<ref
target="#_idTextAnchor036"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Georgalis 2022)</hi
></ref
>. Most notably from a geographic point of view, the Eastern portions of the continent remain notably less sampled for fossil snakes than Western and Central Europe (e.g. <ref
target="#_idTextAnchor016"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Ivanov 2022</hi
></ref
>; <ref
target="#_idTextAnchor036"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Smith &amp; Georgalis 2022)</hi
></ref
>.</p
><p
style="txt_Normal"
>European snake fossils have been known for over two centuries, with the earliest discoveries dating back to the early 19th century (<ref
target="#_idTextAnchor018"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Karg 1805)</hi
></ref
>. Throughout that century, notable fossil snake discoveries continued to capture the interest of European palaeontologists, including remarkable or enigmatic forms, such as the giant aquatic genus <hi
rend="italic"
style="typo_Italique"
>Palaeophis </hi
>Owen, 1841, from England, the giant viper <hi
rend="italic"
style="typo_Italique"
>Laophis </hi
>Owen, 1857, and <hi
rend="italic"
style="typo_Italique"
>Python euboicus </hi
>Römer, 1870 – representing the first record of the extant genus <hi
rend="italic"
style="typo_Italique"
>Python </hi
>Daudin, 1803, in Europe – both from Greece, as well as the constrictor <hi
rend="italic"
style="typo_Italique"
>Palaeopython </hi
>Rochebrune, 1880, from France (<ref
target="#_idTextAnchor022"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Owen 1841</hi
></ref
>, <ref
target="#_idTextAnchor023"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1850</hi
></ref
>, <ref
target="#_idTextAnchor024"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1857</hi
></ref
>; <ref
target="#_idTextAnchor021"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Meyer 1845</hi
></ref
>; <ref
target="#_idTextAnchor033"
><hi
rend="underline"
style="typo_souligne"
>Römer 1870</hi
></ref
>; <ref
target="#_idTextAnchor005"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Filhol 1877</hi
></ref
>; <ref
target="#_idTextAnchor031"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rochebrune 1880</hi
></ref
>, <ref
target="#_idTextAnchor032"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1884)</hi
></ref
>. The 20th century witnessed continued advancements in fossil snake discoveries in Europe, driven particularly by the comprehensive and meticulous work of Robert Hoffstetter, Jean-Claude Rage, and Zbigniew Szyndlar, who significantly enhanced our understanding of taxonomic diversity, cranial and vertebral diagnostic features, and intracolumnar variation in snakes (e.g. <ref
target="#_idTextAnchor012"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Hoffstetter 1939</hi
></ref
>; <ref
target="#_idTextAnchor014"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Hoffstetter &amp; Rage 1972</hi
></ref
>; <ref
target="#_idTextAnchor026"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Rage 1974</hi
></ref
>, <ref
target="#_idTextAnchor028"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1983</hi
></ref
>, <ref
target="#_idTextAnchor029"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1984</hi
></ref
>; <ref
target="#_idTextAnchor041"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar 1984</hi
></ref
>, <ref
target="#_idTextAnchor042"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1991a</hi
></ref
>, <ref
target="#_idTextAnchor043"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>1991b)</hi
></ref
>. In recent decades, our understanding of the taxonomic diversity and anatomy of Cenozoic fossil snakes from Europe has accelerated significantly, aided by the use of recent technologies such as micro-computed tomography (μCT) scanning (<ref
target="#_idTextAnchor002"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Bell et al. 2021)</hi
></ref
> and by an improved knowledge of the skeletal anatomy of extant taxa (<ref
target="#_idTextAnchor050"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Zaher et al. 2019</hi
></ref
>; <ref
target="#_idTextAnchor046"
type="bibl"
><hi
rend="underline"
style="typo_souligne"
>Szyndlar &amp; Georgalis 2023)</hi
></ref
>. Despite these advances, significant gaps remain, as many taxa have yet to be adequately described and the phylogenetic relationships of several groups are still poorly understood, hindering a full understanding of snake evolution in the European Cenozoic.</p
><p
style="txt_Normal"
>With this new volume in <hi
rend="italic"
style="typo_Italique"
>Comptes Rendus Palevol</hi
>, we aim to address significant gaps in our knowledge of the snake fossil record during the European Cenozoic. The forthcoming contributions in this volume will encompass a range of topics, including:</p
><p
style="txt_Normal"
>– descriptions of new taxa and revisions of poorly documented taxa;</p
><p
style="txt_Normal"
>– identifications of novel anatomical features in the skull and vertebrae of fossil snakes;</p
><p
style="txt_Normal"
>– studies of articulated skeletons from Fossillagerstätte localities, enhanced by the application of micro-computed tomography (μCT) scanning;</p
><p
style="txt_Normal"
>– documentation of new fossil snake occurrences from underexplored regions of Europe;</p
><p
style="txt_Normal"
>– revised taxonomic frameworks for enigmatic and previously ambiguous extinct snake groups;</p
><p
style="txt_Normal"
>– studies of palaeobiogeography, dispersal events, extinction and survivorship dynamics of snakes across the Cenozoic of Europe, using sophisticated analytical methods.</p
><p
style="txt_Normal"
>We anticipate that this volume will provide fresh perspectives on the evolution of Cenozoic snakes in Europe, while also serving as a trigger for future research and new discoveries about these fascinating and charismatic reptiles!</p
><figure
xml:id="_idTextAnchor051"
><graphic
url="../icono/br/Fig1_.jpg"
></graphic
><head
style="titre_figure"
><hi
rend="small-caps"
style="typo_SC"
>Fig. 1</hi
>. — Selected type specimens of European Cenozoic snakes: <hi
rend="bold"
style="typo_gras"
>A</hi
>, paratype skeleton (HLMD-Be 165) of <hi
rend="italic"
style="typo_Italique"
>Messelopython freyi </hi
>Zaher &amp; Smith, 2020, from the early to middle Eocene of Messel, Germany; <hi
rend="bold"
style="typo_gras"
>B</hi
>, holotype skeleton (SMF-ME 1828 A-B) of <hi
rend="italic"
style="typo_Italique"
>Messelophis variatus</hi
> Baszio, 2004, from the early to middle Eocene of Messel, Germany; <hi
rend="bold"
style="typo_gras"
>C</hi
>, syntype trunk vertebra (NHMUK PV OR 33209) of <hi
rend="italic"
style="typo_Italique"
>Palaeophis typhaeus</hi
> Owen, 1850, in right lateral view, from the early Eocene of Bracklesham, England; <hi
rend="bold"
style="typo_gras"
>D</hi
>, holotype trunk vertebra (ISEZ FR/RKI-10000) of <hi
rend="italic"
style="typo_Italique"
>Natrix longivertebrata</hi
> Szyndlar, 1984, in right lateral view, from the Late Pliocene (MN 16), of R<hi
rend="italic"
style="typo_Italique"
>ę</hi
>bielice Królewskie lA, Poland; <hi
rend="bold"
style="typo_gras"
>E</hi
>, holotype trunk vertebra (MNHN.F.<ref
target="http://coldb.mnhn.fr/CatalogNumber/MNHN/F/VCO29"
><hi
rend="underline"
style="typo_souligne"
>VCO29</hi
></ref
>) of <hi
rend="italic"
style="typo_Italique"
>Python europaeus</hi
> Szyndlar &amp; Rage, 2003, in dorsal view, from the Early-Middle Miocene (MN 4/5) of Vieux-Collonges, France; <hi
rend="bold"
style="typo_gras"
>F</hi
>, syntype trunk vertebra (MNHN.F.<ref
target="http://coldb.mnhn.fr/CatalogNumber/MNHN/F/LGA53"
><hi
rend="underline"
style="typo_souligne"
>LGA53</hi
></ref
>) of “<hi
rend="italic"
style="typo_Italique"
>Typhlops</hi
>”<hi
rend="italic"
style="typo_Italique"
> grivensis</hi
> Hoffstetter, 1946, in dorsal view, from the Middle Miocene (MN 7/8) of La Grive, France; <hi
rend="bold"
style="typo_gras"
>G</hi
>, holotype trunk vertebra (MNHN.F.<ref
target="http://coldb.mnhn.fr/CatalogNumber/MNHN/F/CB1603"
><hi
rend="underline"
style="typo_souligne"
>CB1603</hi
></ref
>) of <hi
rend="italic"
style="typo_Italique"
>Russellophis tenuis</hi
> Rage, 1975, in ventral view, from the early Eocene (MP 8/9) of Condé-en-Brie, France; <hi
rend="bold"
style="typo_gras"
>H</hi
>, right maxilla (GMH Ce I-5826-1926) part of the lectotype of <hi
rend="italic"
style="typo_Italique"
>Eoconstrictor spinifer</hi
> (Barnes, 1927), in labial view, from the late early to early middle Eocene of Geiseltal, Germany; <hi
rend="bold"
style="typo_gras"
>I</hi
>, holotype trunk vertebra (PIMUZ A/III 634) of <hi
rend="italic"
style="typo_Italique"
>Palaeopython helveticus</hi
> Georgalis &amp; Scheyer, 2019, in anterior view, from the late middle to late Eocene of Dielsdorf, Switzerland; <hi
rend="bold"
style="typo_gras"
>J</hi
>, paralectotype mummified trunk portion (MNHN.F.<ref
target="http://coldb.mnhn.fr/CatalogNumber/MNHN/F/QU16329"
><hi
rend="underline"
style="typo_souligne"
>QU16329</hi
></ref
>) of <hi
rend="italic"
style="typo_Italique"
>Rageophis lafonti</hi
> (Filhol, 1877) from the Eocene of the Phosphorites du Quercy, France (this specimen serves also as a paralectotype of <hi
rend="italic"
style="typo_Italique"
>Tachyophis nitidus </hi
>Rochebrune, 1884); <hi
rend="bold"
style="typo_gras"
>K</hi
>, holotype posterior caudal vertebra (MNHN.F.<ref
target="http://coldb.mnhn.fr/CatalogNumber/MNHN/F/COD1"
><hi
rend="underline"
style="typo_souligne"
>COD1</hi
></ref
>) of <hi
rend="italic"
style="typo_Italique"
>Bransateryx vireti</hi
> Hoffstetter &amp; Rage, 1972, in anterior view, from the late Oligocene (MP 30) of Coderet, France; <hi
rend="bold"
style="typo_gras"
>L</hi
>, paralectotype left dentary (MNHN.F.<ref
target="http://coldb.mnhn.fr/CatalogNumber/MNHN/F/QU16336"
><hi
rend="underline"
style="typo_souligne"
>QU16336</hi
></ref
>) of <hi
rend="italic"
style="typo_Italique"
>Palaelaphis antiquus</hi
> Rochebrune, 1884, in medial view, from the Eocene or Oligocene of the Phosphorites du Quercy, France. Collections: A, Hessisches Landesmuseum Darmstadt; B, Senckenberg Forschungsinstitut und Naturmuseum, Frankfurt am Main, C, Natural History Museum, London, D, Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Krakow; E-G, J-L, ­Muséum national d’Histoire naturelle, Paris; H, Geiseltalmuseum of Martin-Luther Universität Halle-Wittenberg, Halle; I, Palaeontological Institute of the University of Zurich. Scale bars: A, 50 mm; B, 40 mm; C, J, 10 mm; D, F, 1 mm; E, 3 mm; G, K, 2 mm; H, I, L, 5 mm. Photo credits: A, HZ; B, Anika Vogel; C-L, GLG.</head
></figure
><div
type="section1"
><head
style="T_1"
subtype="level1"
>Acknowledgements</head
><p
style="txt_Normal"
>For access to specimens under their care, we thank Nour-­Eddine Jalil (MNHN), Marc Jones and Mike Day (NHMUK), Krister Smith (SMF-ME), Oliver Wings and Roberto Rozzi (GMH), Christian Klug (PIMUZ), and Torsten Wappler (HLMD). GLG acknowledges funding from the research project no. 2023/49/B/ST10/02631 financed by the National Science Center of Poland (Narodowe Centrum Nauki), as well as travel support from SYNTHESYS FR-TAF_Call4_035 (MNHN) and the 2023 Richard Owen Fund of the Palaeontographical Society.</p
></div
></div
></body
><back
><div
type="bibliographie"
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