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International audience; The flowering plant family Annonaceae includes important commercially grown tropical crops, but development of promising species is hindered by a lack of genomic resources to build breeding programs. Annonaceae are part of the magnoliids, an ancient lineage of angiosperms for which evolutionary relationships with other major clades remain unclear. To provide resources to breeders and evolutionary researchers, we report a chromosome-level genome assembly of the soursop (Annona muricata). We assembled the genome using 444.32 Gb of DNA sequences (676x sequencing depth) from PacBio and Illumina short-reads, in combination with 10x Genomics and Bionano data (v1). A total of 949 scaffolds were assembled to a final size of 656.77 Mb, with a scaffold N50 of 3.43 Mb (v1), and then further improved to seven pseudo-chromosomes using Hi-C sequencing data (v2; scaffold N50: 93.2 Mb, total size in chromosomes: 639.6 Mb). Heterozygosity was very low (0.06%), while repeat sequences accounted for 54.87% of the genome, and 23,375 protein-coding genes with an average of 4.79 exons per gene were annotated using de novo, RNA-seq and homology-based approaches. Reconstruction of the historical population size showed a slow continuous contraction, probably related to Cenozoic climate changes. The soursop is the first genome assembled in Annonaceae, supporting further studies of floral evolution in magnoliids, providing an essential resource for delineating relationships of ancient angiosperm lineages. Both genome-assisted improvement and conservation efforts will be strengthened by the availability of the soursop genome. As a community resource, this assembly will further strengthen the role of Annonaceae as model species for research on the ecology, evolution and domestication potential of tropical species in pomology and agroforestry.

The question of the origin of petals has long been debated in the botanical literature. Ranunculales are characterized by a spectacular floral diversity, particularly at the perianth level. Recent progress in understanding the genetic bases of floral organ identity suggests a single origin for petals in Ranunculaceae, contrasting with the traditional morphological hypothesis of repeated evolution. However, perianth evolution at the ordinal level remains incompletely understood. Recent advances in the elucidation of phylogenetic relationships in the order now provide a new opportunity to study character evolution with model-based methods. We used ancestral state reconstruction methods that take into account various sources of uncertainty to reconstruct the evolution of floral traits at the scale of Ranunculales using a consensus phylogenetic framework of 144 terminal species representing all families in the order. Ancestrally, Ranunculales probably had three trimerous whorls of perianth organs differentiated into two categories of petaloid organs differing in their shape. Each whorl was further lost or duplicated. Moreover, our results support the hypothesis of a single origin of highly specialized (elaborate) nectariferous petals in Ranunculaceae.

AimLong‐distance dispersal has contributed to the disjunct biogeographical distribution of rain forest plants—something that has fascinated biogeographers since Humboldt's time. However, the dispersal agent for these tropical plant lineages remains puzzling. Here, we investigate which frugivory‐related traits may have facilitated past intercontinental long‐distance dispersal in the custard apple family (Annonaceae), a major vertebrate‐dispersed tropical plant family. We hypothesize that long‐distance dispersal was associated with the evolution of traits related to dispersal by large‐bodied mammals (e.g., large, dull‐coloured, “megafaunal” fruits) and strong‐flying, ocean‐crossing birds and bats (e.g., dehiscent, moniliform or cauliflorous fruits).LocationGlobal.TaxonAnnonaceae.MethodsWe used a fossil‐calibrated phylogenetic framework to infer the biogeographic history of 234 Annonaceae species (10%, covering nearly all genera) in relation to the evolution of 15 frugivory‐related traits, using maximum likelihood and Bayesian inferences. Furthermore, we used linear and generalized linear models and phylogenetic simulations to test whether ancestral fruit traits during intercontinental dispersal were different from those of other lineages not involved in long‐distance dispersal.ResultsWe inferred the ancestral Annonaceae fruits to be small with a single or few small seeds and a small number of fruitlets. These fruits were most probably apocarpous, indehiscent and/or moniliform (i.e., long beads of fruitlets). Furthermore, most of the long‐distance dispersal events in Annonaceae occurred via the expanded tropical forests in the Early Cenozoic (“geodispersal”), and were significantly associated with large (c. 3 cm long), dull‐coloured fruits and short stipes. Additionally, long‐distance dispersal was also facilitated by dehiscent, moniliform and non‐cauliflorous fruits.Main conclusionsWe suggest that the evolution of frugivory‐related traits associated with dispersal by frugivores that frequently move across large distances and/or barriers, such as large‐bodied mammals and strong‐flying birds, has contributed to the disjunct tropical biogeographical distribution of Annonaceae, and probably of tropical rain forest plants more generally.

International audience; Proteaceae are a basal eudicot family with a highly conserved floral groundplan but which displays considerable variation in other aspects of floral and inflorescence morphology. Their morphological diversity and phylogenetic position make them good candidates for understanding the evolution of floral architecture, in particular the question of the homology of the undifferentiated perianth with the differentiated perianth of core eudicots, and the mechanisms underlying the repeated evolution of zygomorphy. In this paper, we combine a morphological approach to explore floral ontogenesis and a transcriptomic approach to access the genes involved in floral organ identity and development, focusing on Grevillea juniperina, a species from subfamily Grevilleoideae. We present developmental data for Grevillea juniperina and three additional species that differ in their floral symmetry using stereomicroscopy, SEM and High Resolution X-Ray Computed Tomography. We find that the adnation of stamens to tepals takes place at early developmental stages, and that the establishment of bilateral symmetry coincides with the asymmetrical growth of the single carpel. To set a framework for understanding the genetic basis of floral development in Proteaceae, we generated and annotated de novo a reference leaf/flower transcriptome from Grevillea juniperina. We found Grevillea homologs of all lineages of MADS-box genes involved in floral organ identity. Using Arabidopsis thaliana gene expression data as a reference, we found homologs of other genes involved in floral development in the transcriptome of G. juniperina. We also found at least 21 class I and class II TCP genes, a gene family involved in the regulation of growth processes, including floral symmetry. The expression patterns of a set of floral genes obtained from the transcriptome were characterized during floral development to assess their organ specificity and asymmetry of expression.

Targeted enrichment and sequencing of hundreds of nuclear loci for phylogenetic reconstruction is becoming an important tool for plant systematics and evolution. Annonaceae is a major pantropical plant family with 109 genera and ca. 2450 species, occurring across all major and minor tropical forests of the world. Baits were designed by sequencing the transcriptomes of five species from two of the largest Annonaceae subfamilies. Orthologous loci were identified. The resulting baiting kit was used to reconstruct phylogenetic relationships at two different levels using concatenated and gene tree approaches: a family wide Annonaceae analysis sampling 65 genera and a species level analysis of tribe Piptostigmateae sampling 29 species with multiple individuals per species. DNA extraction was undertaken mainly on silicagel dried leaves, with two samples from herbarium dried leaves. Our kit targets 469 exons (364 653 bp of sequence data), successfully capturing sequences from across Annonaceae. Silicagel dried and herbarium DNA worked eaually well. We present for the first time a nuclear gene-based phylogenetic tree at the generic level based on 317 supercontigs. Results mainly confirm previous chloroplast based studies. However, several new relationships are found and discussed. We show significant differences in branch lengths between the two large subfamilies Annonoideae and Malmeoideae. A new tribe, Annickieae, is erected containing a single African genus Annickia. We also reconstructed a well resolved species-level phylogenetic tree of the Piptostigmteae tribe. Our baiting kit is useful for reconstructing well supported phylogenetic relationships within Annonaceae at different taxonomic levels. The nuclear genome is mainly concordant with plastome information with a few exceptions. Moreover, we find that substitution rate heterogeneity between the two subfamilies is also found within the nuclear compartment, and not just plastomes and ribosomal DNA as previously shown. Our results have implications for understanding the biogeography, molecular dating and evolution of Annonaceae.

International audience; A recommendation of the preprint: Pirie MD, Maas PJM, Wilschut RA, Melchers-Sharrott H, Chatrou LW. 2017. Parallel diversifications of Cremastosperma and Mosannona (Annonaceae), tropical rainforest trees tracking Neogene upheaval of the South American continent. BioRxiv 141127, http://dx.doi.org/10.1101/141127

center dot Background and Aims The basal eudicot family Proteaceae (approx. 1700 species) shows considerable variation in floral symmetry but has received little attention in studies of evolutionary development at the genetic level. A framework for understanding the shifts in floral symmetry in Proteaceae is provided by reconstructing ancestral states on an upated phylogeny of the family, and homologues of CYCLOIDEA (CYC), a key gene for the control of floral symmetry in both monocots and eudicots, are characterized. center dot Methods Perianth symmetry transitions were reconstructed on a new species-level tree using parsimony and maximum likelihood. CYC-like genes in 35 species (31 genera) of Proteaceae were sequenced and their phylogeny was reconstructed. Shifts in selection pressure following gene duplication were investigated using nested branch-site models of sequence evolution. Expression patterns of CYC homologues were characterized in three species of Grevillea with different types of floral symmetry. center dot Key Results Zygomorphy has evolved 10-18 times independently in Proteaceae from actinomorphic ancestors, with at least four reversals to actinomorphy. A single duplication of CYC-like genes occurred prior to the diversification of Proteaceae, with putative loss or divergence of the ProtCYC1 paralogue in more than half of the species sampled. No shifts in selection pressure were detected in the branches subtending the two ProtCYC paralogues. However, the amino acid sequence preceding the TCP domain is strongly divergent in Grevillea ProtCYC1 compared with other species. ProtCYC genes were expressed in developing flowers of both actinomorphic and zygomorphic Grevillea species, with late asymmetric expression in the perianth of the latter. center dot Conclusion Proteaceae is a remarkable family in terms of the number of transitions in floral symmetry. Furthermore, although CYC-like genes in Grevillea have unusual sequence characteristics, they display patterns of expression that make them good candidates for playing a role in the establishment of floral symmetry.

International audience; Background and Aims Fumarioideae (20 genera, 593 species) is a clade of Papaveraceae (Ranunculales) characterized by flowers that are either disymmetric (i.e. two perpendicular planes of bilateral symmetry) or zygomorphic (i.e. one plane of bilateral symmetry). In contrast, the other subfamily of Papaveraceae, Papaveroideae (23 genera, 230 species), has actinomorphic flowers (i.e. more than two planes of symmetry). Understanding of the evolution of floral symmetry in this clade has so far been limited by the lack of a reliable phylogenetic framework. Pteridophyllum (one species) shares similarities with Fumarioideae but has actinomorphic flowers, and the relationships among Pteridophyllum, Papaveroideae and Fumarioideae have remained unclear. This study reassesses the evolution of floral symmetry in Papaveraceae based on new molecular phylogenetic analyses of the family. Methods : Maximum likelihood, Bayesian and maximum parsimony phylogenetic analyses of Papaveraceae were conducted using six plastid markers and one nuclear marker, sampling Pteridophyllum, 18 (90 %) genera and 73 species of Fumarioideae, 11 (48 %) genera and 11 species of Papaveroideae, and a wide selection of outgroup taxa. Floral characters recorded from the literature were then optimized onto phylogenetic trees to reconstruct ancestral states using parsimony, maximum likelihood and reversible-jump Bayesian approaches. Key Results : Pteridophyllum is not nested in Fumarioideae. Fumarioideae are monophyletic and Hypecoum (18 species) is the sister group of the remaining genera. Relationships within the core Fumarioideae are well resolved and supported. Dactylicapnos and all zygomorphic genera form a well-supported clade nested among disymmetric taxa. Conclusions : Disymmetry of the corolla is a synapomorphy of Fumarioideae and is strongly correlated with changes in the androecium and differentiation of middle and inner tepal shape (basal spurs on middle tepals). Zygomorphy subsequently evolved from disymmetry either once (with a reversal in Dactylicapnos) or twice (Capnoides, other zygomorphic Fumarioideae) and appears to be correlated with the loss of one nectar spur.

Angiosperms are the most diversified clade of extant plants and are exceptionally species-rich in tropical regions. In this thesis, I investigated breeding system evolution and biogeographic history in the family Moraceae, which I used as a model clade to understand the origin and evolution of diversity of angiosperms. In Chapter I, I reconstructed and calibrated a new dated phylogenetic tree for Moraceae as a whole. I then used this tree to reconstruct ancestral states of breeding systems in Moraceae and Ficus. The crown group ages of Moraceae and Ficus were estimated in the Cretaceous and in the Eocene, respectively. Dioecy was inferred as the ancestral breeding systems of Moraceae, with several subsequent transitions to monoecy, including in Ficus. This result suggests that dioecy is not necessarily an evolutionary dead end. In Chapter II, I reconstructed a dated phylogenetic tree for tribe Dorstenieae, mainly distributed in tropical regions, with a new data set of nuclear genomic data generated with a Hyb-Seq approach. Biogeographic history was then reconstructed using dispersal-extinction-cladogenesis models. The crown group ages of Dorstenieae and Dorstenia were estimated in the Cretaceous and in the Cretaceous/Paleocene period, respectively. Two long-distance dispersal events from continental Africa to South America occurred in the Cenozoic (Dorstenia and Brosimum s.l.). In Chapter III, I tested the climatic niche difference (temperature and precipitation) between the two breeding systems (monoecy and gynodioecy) in Ficus using a new dataset of cleaned spatial occurrence records and breeding systems for 183 species. I used two comparative approaches: generalized estimating equations (GEE) and generalized linear models (GLM). A positive relationship between precipitation and gynodioecy was supported by GLM, but not GEE analyses, and no relationship between temperature and breeding systems was supported by either method. Higher dispersal ability and the potential for self-fertilization may explain why monoecious species of Ficus have been able to colonize and survive in drier environments. This thesis highlights the potential of phylogenetic comparative methods and phylogenomic data to address questions of breeding system evolution and biogeography in Moraceae, and opens up several important new perspectives worth investigating in other plant clades, such as a relationship between breeding system and climatic niche.; Les Angiospermes sont le clade le plus diversifié des plantes actuelles et sont exceptionnellement riches en espèces dans les régions tropicales. Dans cette thèse, j’ai étudié l’évolution des systèmes sexuels et l’histoire biogéographique de la famille des Moraceae, clade modèle utilisé pour comprendre l’origine et l’évolution de la diversité chez les Angiospermes. Dans le Chapitre I, j’ai reconstruit et calibré un nouvel arbre phylogénétique daté pour les Moraceae. J’ai ensuite utilisé cet arbre pour reconstruire les états ancestraux des systèmes sexuels chez les Moraceae et Ficus. Les âges des groupes-couronne des Moraceae et du genre Ficus sont estimés au Crétacé et à l’Eocène, respectivement. La dioécie est inférée comme l’état ancestral des systèmes sexuels chez les Moraceae, avec plusieurs transitions ultérieures vers la monoécie, y compris chez Ficus. Ce résultat suggère que la dioécie ne représente pas nécessairement un cul-de-sac évolutif. Dans le Chapitre II, j’ai reconstruit un arbre phylogénétique daté pour la tribu des Dorstenieae, distribuée principalement dans les régions tropicales, à partir d’un nouveau jeu de données génomiques nucléaires produit avec une approche Hyb-Seq. L’histoire biogéographique du groupe a ensuite été reconstruite en utilisant les modèles de dispersion-extinction-cladogenèse. Les âges des groupes-couronne des Dorstenieae et du genre Dorstenia sont estimés au Crétacé et dans la période du Crétacé au Paléocène, respectivement. Deux évènements de dispersion à longue distance depuis l’Afrique continentale vers l’Amérique du Sud ont eu lieu au Cénozoïque (Dorstenia et Brosimum s.l.). Dans le Chapitre III, j’ai testé les différences de niche climatique (température et précipitation) entre les deux systèmes sexuels (monoécie et gynodioécie) chez Ficus avec un nouveau jeu de données fiables d’occurrences spatiales et de systèmes sexuels chez 183 espèces. À cette fin, j’ai utilisé deux approches comparatives : équations d’estimation généralisées (GEE) et modèles linéaires généralisés (GLM). Une relation positive entre précipitation et gynodioécie est soutenue par les analyses GLM, et aucune méthode ne soutient une relation entre température et système sexuel. Une meilleure capacité à se disperser et le potentiel d’autopollinisation sont deux explications possibles pour la colonisation et la survie des espèces monoïques dans des environnements plus secs. Cette thèse démontre le potentiel des méthodes phylogénétiques comparatives et des données phylogénomiques pour répondre aux questions d’évolution des systèmes sexuels et de biogéographie chez les Moraceae et ouvre plusieurs nouvelles perspectives importantes méritant d’être approfondies chez d’autres clades de plantes, telles que la relation entre système sexuel et niche climatique.

Deep phylogenetic relationships in the angiosperms had long been uncertain. However, by the end of the 1990s, large-scale studies contributed to the current well resolved picture of the tree of flowering plants, in which eudicots, monocots, and magnoliids are the three largest clades. Whereas monocots and eudicots have been recognized since the very first phylogenetic analyses, the monophyly of magnoliids (Canellales, Laurales, Magnoliales, and Piperales) is a more recent result. Magnoliidae, as now circumscribed, consist of 20 families and ca. 10,000 species mostly distributed in the tropics. Before the present thesis, several parts of the magnoliid tree had been well studied, but little was known about the evolutionary history of Magnoliidae as a whole. The first chapter of this thesis is a phylogenetic study conducted to clarify the relationships among families and orders of Magnoliidae. To do so, I sampled 199 species of Magnoliidae and 12 molecular markers from the three genomes and conducted phylogenetic analyses using parsimony, maximum likelihood, and Bayesian methods. The results confirm, with a greater level of support, two clades in Magnoliidae: Canellale + Piperales, and Laurales + Magnoliales. In addition, the relationships among the 20 families are generally well supported, and Lactoridaceae and Hydnoraceae are nested within Aristolochiaceae (Piperales). In the second chapter, the ages and phylogenetic positions of 10 fossils attributed to Magnoliidae were reviewed in detail. The goal of this study was to provide new reliable calibration points in order to conduct molecular dating analyses. These fossils were selected from the rich fossil record of the group because of their previous inclusion in phylogenetic analyses with extant taxa. The resulting calibration scheme provides six solid, internal minimum age constraints. The third chapter includes molecular dating analyses using the present calibration scheme and the same molecular dataset of Chapter 1. This study tends to push back in time the ages of the crown nodes of Magnoliidae (127.1-198.9 Ma), and of the four orders, Canellales (126.3-141.0 Ma), Piperales (88.2-157.7 Ma), Laurales (111.8-165.6 Ma), and Magnoliales (115.0-164.2 Ma). In the same chapter, I investigated the mode of diversification in the group. The strongly imbalanced distribution of species appears to be best explained by models of diversification with 6 to 14 diversification rate shifts. Finally, in the last chapter, I traced the evolution of 26 floral characters to reconstruct the ancestral flowers in key nodes of Magnoliidae. I used the phylogeny of Chapter 1 and an exemplar approach. Our results show that the most recent common ancestor of all Magnoliidae was a tree bearing actinomorphic, bisexual flowers with a differentiated perianth of two alternate, trimerous whorls of free perianth parts (outer and inner tepals) and probably three free stamens. This work provides key results on the evolution of Magnoliidae and raises several new questions such as the impact of geological crises on diversification of the group or the influence of pollinators and the environment on the evolution of floral morphology.; Les relations de parentés profondes au sein des Angiospermes ont été longtemps incertaines. A la fin des années 90, les études phylogénétiques à grande échelle ont contribué à l’obtention de l’arbre actuel des Plantes à fleurs, dans lequel Eudicotylédones, Monocotylédones et Magnoliidae forment les trois plus grands clades. Contrairement aux Monocotylédones et aux Eudicotylédones, la monophylie des Magnoliidae (Canellales, Laurales, Magnoliales et Piperales) n’a été soutenue que plus récemment. Les Magnoliidae contiennent actuellement 20 familles et environ 10 000 espèces majoritairement présentes sous les tropiques. Avant cette thèse, de nombreuses parties de ce groupe avaient été étudiées en détail mais l’histoire évolutive du groupe dans son ensemble était encore mal connue. Le premier chapitre est une étude phylogénétique des relations entre les familles et les ordres de Magnoliidae. Pour réaliser cette étude, j’ai échantillonné 199 espèces du groupe et 12 marqueurs moléculaires issus des trois génomes. J’ai ensuite mené des analyses phylogénétiques avec les méthodes de parcimonie, d’inférence bayésienne et de maximum de vraisemblance. Les résultats confirment avec un plus fort soutien la présence de deux clades dans ce groupe : Canellales + Piperales et Laurales + Magnoliales. De plus, les relations entre les 20 familles sont généralement bien soutenues, les Lactoridaceae et les Hydnoraceae étant incluses dans les Aristolochiaceae (Piperales). Dans le second chapitre, j’ai révisé l’âge et la position de 10 fossiles identifiés comme appartenant aux Magnoliidae. Le but de cette étude était de fournir de nouveaux points de calibration fiables afin de conduire de nouvelles analyses de datation moléculaire. Parmi les nombreux fossiles du groupe, nous avons choisi ces espèces car elles avaient été placées phylogénétiquement par des études antérieures. Le schéma de calibration résultant de ce travail inclut six contraintes fiables d’âges minimum. Le troisième chapitre est une étude de datation moléculaire utilisant ce schéma de calibration et le même jeu de données moléculaires que le chapitre 1. Les résultats tendent à repousser l’âge des Magnoliidae (127.1-198.9 Ma), et des quatre ordres Canellales (126.3-141.0 Ma), Piperales (88.2-157.7 Ma), Laurales (111.8-165.6 Ma) et Magnoliales (115.0-164.2 Ma). Dans ce même chapitre, j’ai également étudié le mode de diversification du groupe. Les variations importantes du nombre d’espèces entre les différentes parties de l’arbre s’expliquent le mieux par des modèles de diversification incluant 6 à 14 transition du taux net de diversification. Enfin, dans le dernier chapitre de la thèse, j’ai retracé l’histoire évolutive de 26 caractères floraux pour reconstruire les fleurs ancestrales de nœuds-clés des Magnoliidae. Pour ce faire, j’ai tiré parti de la phylogénie du premier chapitre et utilisé les mêmes espèces dans ma matrice morphologique. Les résultats montrent que l’ancêtre commun le plus récent des Magnoliidae présentait des fleurs bisexuées et actinomorphes avec un périanthe différencié de deux cycles trimères à tépales libres et probablement trois étamines libres. Ce travail de thèse apporte des résultats importants sur l’évolution des Magnoliidae et soulève de nombreuses questions telles que l’impact des crises géologiques sur la diversification du groupe ou l’influence des pollinisateurs et de l’environnement sur l’évolution de la morphologie florale.

Deep phylogenetic relationships in the angiosperms had long been uncertain. However, by the end of the 1990s, large-scale studies contributed to the current well resolved picture of the tree of flowering plants, in which eudicots, monocots, and magnoliids are the three largest clades. Whereas monocots and eudicots have been recognized since the very first phylogenetic analyses, the monophyly of magnoliids (Canellales, Laurales, Magnoliales, and Piperales) is a more recent result. Magnoliidae, as now circumscribed, consist of 20 families and ca. 10,000 species mostly distributed in the tropics. Before the present thesis, several parts of the magnoliid tree had been well studied, but little was known about the evolutionary history of Magnoliidae as a whole. The first chapter of this thesis is a phylogenetic study conducted to clarify the relationships among families and orders of Magnoliidae. To do so, I sampled 199 species of Magnoliidae and 12 molecular markers from the three genomes and conducted phylogenetic analyses using parsimony, maximum likelihood, and Bayesian methods. The results confirm, with a greater level of support, two clades in Magnoliidae: Canellale + Piperales, and Laurales + Magnoliales. In addition, the relationships among the 20 families are generally well supported, and Lactoridaceae and Hydnoraceae are nested within Aristolochiaceae (Piperales). In the second chapter, the ages and phylogenetic positions of 10 fossils attributed to Magnoliidae were reviewed in detail. The goal of this study was to provide new reliable calibration points in order to conduct molecular dating analyses. These fossils were selected from the rich fossil record of the group because of their previous inclusion in phylogenetic analyses with extant taxa. The resulting calibration scheme provides six solid, internal minimum age constraints. The third chapter includes molecular dating analyses using the present calibration scheme and the same molecular dataset of Chapter 1. This study tends to push back in time the ages of the crown nodes of Magnoliidae (127.1-198.9 Ma), and of the four orders, Canellales (126.3-141.0 Ma), Piperales (88.2-157.7 Ma), Laurales (111.8-165.6 Ma), and Magnoliales (115.0-164.2 Ma). In the same chapter, I investigated the mode of diversification in the group. The strongly imbalanced distribution of species appears to be best explained by models of diversification with 6 to 14 diversification rate shifts. Finally, in the last chapter, I traced the evolution of 26 floral characters to reconstruct the ancestral flowers in key nodes of Magnoliidae. I used the phylogeny of Chapter 1 and an exemplar approach. Our results show that the most recent common ancestor of all Magnoliidae was a tree bearing actinomorphic, bisexual flowers with a differentiated perianth of two alternate, trimerous whorls of free perianth parts (outer and inner tepals) and probably three free stamens. This work provides key results on the evolution of Magnoliidae and raises several new questions such as the impact of geological crises on diversification of the group or the influence of pollinators and the environment on the evolution of floral morphology.; Les relations de parentés profondes au sein des Angiospermes ont été longtemps incertaines. A la fin des années 90, les études phylogénétiques à grande échelle ont contribué à l’obtention de l’arbre actuel des Plantes à fleurs, dans lequel Eudicotylédones, Monocotylédones et Magnoliidae forment les trois plus grands clades. Contrairement aux Monocotylédones et aux Eudicotylédones, la monophylie des Magnoliidae (Canellales, Laurales, Magnoliales et Piperales) n’a été soutenue que plus récemment. Les Magnoliidae contiennent actuellement 20 familles et environ 10 000 espèces majoritairement présentes sous les tropiques. Avant cette thèse, de nombreuses parties de ce groupe avaient été étudiées en détail mais l’histoire évolutive du groupe dans son ensemble était encore mal connue. Le premier chapitre est une étude phylogénétique des relations entre les familles et les ordres de Magnoliidae. Pour réaliser cette étude, j’ai échantillonné 199 espèces du groupe et 12 marqueurs moléculaires issus des trois génomes. J’ai ensuite mené des analyses phylogénétiques avec les méthodes de parcimonie, d’inférence bayésienne et de maximum de vraisemblance. Les résultats confirment avec un plus fort soutien la présence de deux clades dans ce groupe : Canellales + Piperales et Laurales + Magnoliales. De plus, les relations entre les 20 familles sont généralement bien soutenues, les Lactoridaceae et les Hydnoraceae étant incluses dans les Aristolochiaceae (Piperales). Dans le second chapitre, j’ai révisé l’âge et la position de 10 fossiles identifiés comme appartenant aux Magnoliidae. Le but de cette étude était de fournir de nouveaux points de calibration fiables afin de conduire de nouvelles analyses de datation moléculaire. Parmi les nombreux fossiles du groupe, nous avons choisi ces espèces car elles avaient été placées phylogénétiquement par des études antérieures. Le schéma de calibration résultant de ce travail inclut six contraintes fiables d’âges minimum. Le troisième chapitre est une étude de datation moléculaire utilisant ce schéma de calibration et le même jeu de données moléculaires que le chapitre 1. Les résultats tendent à repousser l’âge des Magnoliidae (127.1-198.9 Ma), et des quatre ordres Canellales (126.3-141.0 Ma), Piperales (88.2-157.7 Ma), Laurales (111.8-165.6 Ma) et Magnoliales (115.0-164.2 Ma). Dans ce même chapitre, j’ai également étudié le mode de diversification du groupe. Les variations importantes du nombre d’espèces entre les différentes parties de l’arbre s’expliquent le mieux par des modèles de diversification incluant 6 à 14 transition du taux net de diversification. Enfin, dans le dernier chapitre de la thèse, j’ai retracé l’histoire évolutive de 26 caractères floraux pour reconstruire les fleurs ancestrales de nœuds-clés des Magnoliidae. Pour ce faire, j’ai tiré parti de la phylogénie du premier chapitre et utilisé les mêmes espèces dans ma matrice morphologique. Les résultats montrent que l’ancêtre commun le plus récent des Magnoliidae présentait des fleurs bisexuées et actinomorphes avec un périanthe différencié de deux cycles trimères à tépales libres et probablement trois étamines libres. Ce travail de thèse apporte des résultats importants sur l’évolution des Magnoliidae et soulève de nombreuses questions telles que l’impact des crises géologiques sur la diversification du groupe ou l’influence des pollinisateurs et de l’environnement sur l’évolution de la morphologie florale.