| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Lionel Cavin | Q22110152 |
| Guillaume Guinot | Q21392380 | ||
| P2860 | cites work | Exploring the effects of phylogenetic uncertainty and consensus trees on stratigraphic consistency scores: a new program and a standardized method | Q57436964 |
| Regional to global patterns in Late Cretaceous selachian (Chondrichthyes, Euselachii) diversity | Q58333489 | ||
| Geologic and Biologic Controls on the Evolution of Reefs | Q58396808 | ||
| Extinction and recovery patterns of scleractinian corals at the Cretaceous-Tertiary boundary | Q58396857 | ||
| The early Toarcian (Early Jurassic) and the Cenomanian–Turonian (Late Cretaceous) mass extinctions: similarities and contrasts | Q58457329 | ||
| Mitogenomic evidence for an Indo-West Pacific origin of the Clupeoidei (Teleostei: Clupeiformes) | Q21003828 | ||
| Phylogenetic interrelationships of ginglymodian fishes (Actinopterygii: Neopterygii) | Q21089864 | ||
| Global patterns and predictors of marine biodiversity across taxa | Q22122181 | ||
| Explosive morphological diversification of spiny-finned teleost fishes in the aftermath of the end-Cretaceous extinction | Q24614560 | ||
| Nine exceptional radiations plus high turnover explain species diversity in jawed vertebrates | Q24645052 | ||
| Ecomorphological selectivity among marine teleost fishes during the end-Cretaceous extinction | Q24649103 | ||
| A phylogenetic analysis of the major groups of catfishes (Teleostei: Siluriformes) using rag1 and rag2 nuclear gene sequences | Q28254862 | ||
| Shark tales: a molecular species-level phylogeny of sharks (Selachimorpha, Chondrichthyes) | Q28299856 | ||
| Fifty million years of herbivory on coral reefs: fossils, fish and functional innovations | Q28657761 | ||
| Evolutionary origin of the Scombridae (tunas and mackerels): members of a paleogene adaptive radiation with 14 other pelagic fish families | Q28681208 | ||
| An analytical approach for estimating fossil record and diversification events in sharks, skates and rays | Q28728062 | ||
| Resolution of ray-finned fish phylogeny and timing of diversification | Q28728276 | ||
| Parallel evolutionary trajectories underlie the origin of giant suspension-feeding whales and bony fishes | Q28732802 | ||
| Evolutionary history of Otophysi (Teleostei), a major clade of the modern freshwater fishes: Pangaean origin and Mesozoic radiation | Q28742308 | ||
| Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes | Q28751601 | ||
| Using ghost lineages to identify diversification events in the fossil record | Q28754612 | ||
| Diversification trajectories and evolutionary life-history traits in early sharks and batoids | Q28754885 | ||
| Fossil ghost ranges are most common in some of the oldest and some of the youngest strata | Q28755283 | ||
| Congruence between phylogenetic and stratigraphic data on the history of life | Q28766150 | ||
| Climate, energy and diversity | Q28766767 | ||
| Geologic constraints on the macroevolutionary history of marine animals | Q28769514 | ||
| A palaeontological and phylogenetical analysis of squaliform sharks (Chondrichthyes: Squaliformes) based on dental characters | Q29308338 | ||
| The Phanerozoic record of global sea-level change | Q29617889 | ||
| An early Cenozoic perspective on greenhouse warming and carbon-cycle dynamics | Q29618074 | ||
| Chronology of fluctuating sea levels since the triassic | Q29618212 | ||
| Determinants of extinction in the fossil record | Q30828797 | ||
| Marine ecology warms up to theory | Q31109374 | ||
| The impact of the pull of the recent on the history of marine diversity | Q31142277 | ||
| The evolutionary origin of flatfish asymmetry | Q31162106 | ||
| Relationships among characiform fishes inferred from analysis of nuclear and mitochondrial gene sequences | Q33215389 | ||
| Temperature control of larval dispersal and the implications for marine ecology, evolution, and conservation | Q33268724 | ||
| Molecular systematics of the gonorynchiform fishes (Teleostei) based on whole mitogenome sequences: implications for higher-level relationships within the Otocephala. | Q54663964 | ||
| A long-bodied centriscoid fish from the basal Eocene of Kabardino-Balkaria, northern Caucasus, Russia. | Q54669668 | ||
| Early fossils illuminate character evolution and interrelationships of Lampridiformes (Teleostei, Acanthomorpha) | Q54745417 | ||
| Morphology, taxonomy, and phylogeny of Triassic pholidophorid fishes (Actinopterygii, Teleostei) | Q54747108 | ||
| †Tingitanius tenuimandibulus,a new platyrhinid batoid from the Turonian (Cretaceous) of Morocco and the cretaceous radiation of the Platyrhinidae | Q54770643 | ||
| Triplomystus applegatei, sp. nov. (Teleostei: Ellimmichthyiformes), a rare “triple armored herring” from El Espinal Quarry (Early Cretaceous), Chiapas, southeastern Mexico | Q54773163 | ||
| Global continental and ocean basin reconstructions since 200Ma | Q55877778 | ||
| A phylogeny of the families of fossil and extant tetraodontiform fishes (Acanthomorpha, Tetraodontiformes), Upper Cretaceous to Recent | Q55898564 | ||
| Early Cretaceous life, climate and anoxia | Q56004943 | ||
| THE SHAPE OF THE PHANEROZOIC MARINE PALAEODIVERSITY CURVE: HOW MUCH CAN BE PREDICTED FROM THE SEDIMENTARY ROCK RECORD OF WESTERN EUROPE? | Q56047677 | ||
| Predictions and tests of climate-based hypotheses of broad-scale variation in taxonomic richness | Q56081563 | ||
| Mass extinctions and sea-level changes | Q56225795 | ||
| The timing of paleoenvironmental change and cause-and-effect relationships during the early Jurassic mass extinction in Europe | Q56332396 | ||
| Life-history correlates of maximum population growth rates in marine fishes | Q56387728 | ||
| Latitudinal Gradients in Species Diversity: The Search for the Primary Cause | Q56387730 | ||
| Anatomy, systematics and phylogeny of both Recent and fossil latid fishes (Teleostei, Perciformes, Latidae) | Q56485207 | ||
| Mid-Cretaceous seafloor spreading pulse: Fact or fiction? | Q56657981 | ||
| A Comprehensive Phylogenetic Study of Amiid Fishes (Amiidae) Based on Comparative Skeletal Anatomy. an Empirical Search for Interconnected Patterns of Natural History | Q56658086 | ||
| Five hundred million years of extinction and recovery: a phanerozoic survey of large-scale diversity patterns in fishes | Q56827245 | ||
| Osteology of Eubiodectes libanicus (Pictet & Humbert, ) and some other ichthyodectiformes (Teleostei): phylogenetic implications | Q56838745 | ||
| The Late Eocene-Oligocene Extinctions | Q56853288 | ||
| Correlation between environment and Late Mesozoic ray-finned fish evolution | Q57235504 | ||
| Do reefs drive diversification in marine teleosts? Evidence from the pufferfishes and their allies (Order Tetraodontiformes). | Q33301520 | ||
| Paleontology. On giant filter feeders | Q33532347 | ||
| Phylogenetic position of the enigmatic Lepidogalaxias salamandroides with comment on the orders of lower euteleostean fishes | Q33646325 | ||
| Estimating divergence times of lizardfishes and their allies (Euteleostei: Aulopiformes) and the timing of deep-sea adaptations | Q33696714 | ||
| Cooler winters as a possible cause of mass extinctions at the Eocene/Oligocene boundary. | Q33923698 | ||
| 100-million-year dynasty of giant planktivorous bony fishes in the Mesozoic seas | Q34021311 | ||
| Coral reefs as drivers of cladogenesis: expanding coral reefs, cryptic extinction events, and the development of biodiversity hotspots | Q34045153 | ||
| Molecular phylogenetic evidence refuting the hypothesis of Batoidea (rays and skates) as derived sharks | Q34174703 | ||
| Faunal turnover of marine tetrapods during the Jurassic-Cretaceous transition | Q34338873 | ||
| The historical biogeography of the freshwater knifefishes using mitogenomic approaches: a mesozoic origin of the Asian notopterids (Actinopterygii: Osteoglossomorpha). | Q34607728 | ||
| Evolution of marine mammals: back to the sea after 300 million years | Q34630375 | ||
| A new phylogeny of tetraodontiform fishes (Tetraodontiformes, Acanthomorpha) based on 22 loci | Q34751915 | ||
| Dating the evolutionary origins of wrasse lineages (Labridae) and the rise of trophic novelty on coral reefs | Q34982685 | ||
| Phylogenetic relationships and timing of diversification in gonorynchiform fishes inferred using nuclear gene DNA sequences (Teleostei: Ostariophysi). | Q35217962 | ||
| Taxonomic review and phylogenetic analysis of Enchodontoidei | Q37889134 | ||
| Major patterns of higher teleostean phylogenies: a new perspective based on 100 complete mitochondrial DNA sequences. | Q38387971 | ||
| Organic carbon fluxes and ecological recovery from the cretaceous-tertiary mass extinction | Q38549777 | ||
| Reconstructing the phylogenetic relationships of the earth's most diverse clade of freshwater fishes--order Cypriniformes (Actinopterygii: Ostariophysi): a case study using multiple nuclear loci and the mitochondrial genome | Q40010537 | ||
| The complex evolutionary history of seeing red: molecular phylogeny and the evolution of an adaptive visual system in deep-sea dragonfishes (Stomiiformes: Stomiidae). | Q42630006 | ||
| Monophyly, phylogenetic position and inter-familial relationships of the Alepocephaliformes (Teleostei) based on whole mitogenome sequences | Q43432360 | ||
| Massive dissociation of gas hydrate during a Jurassic oceanic anoxic event | Q43530841 | ||
| Cretaceous extinctions: evidence overlooked | Q43534517 | ||
| Cretaceous extinctions: multiple causes | Q43534519 | ||
| Cretaceous extinctions: the volcanic hypothesis | Q43534525 | ||
| Body plan convergence in the evolution of skates and rays (Chondrichthyes: Batoidea). | Q44547111 | ||
| Ribosomal RNA genes and deuterostome phylogeny revisited: more cyclostomes, elasmobranchs, reptiles, and a brittle star | Q45820371 | ||
| Evolutionary origin and early biogeography of otophysan fishes (Ostariophysi: Teleostei). | Q46986081 | ||
| Uncertainty in the age of fossils and the stratigraphic fit to phylogenies | Q47194818 | ||
| Mitochondrial molecular clocks and the origin of the major Otocephalan clades (Pisces: Teleostei): A new insight | Q47223867 | ||
| The fossil record and evolution: comparing cladistic and paleontologic evidence for vertebrate history | Q47295101 | ||
| The modified gap excess ratio (GER*) and the stratigraphic congruence of dinosaur phylogenies | Q47632633 | ||
| Phylogenetic relationships among anchovies, sardines, herrings and their relatives (Clupeiformes), inferred from whole mitogenome sequences | Q48083261 | ||
| Amniote Phylogeny and the Importance of Fossils | Q53961449 | ||
| Extinction and environmental change across the Eocene-Oligocene boundary in Tanzania | Q53997701 | ||
| Filling the gap: a fossil frogfish, genus Antennarius (Teleostei, Lophiiformes, Antennariidae), from the Miocene of Algeria | Q54487007 | ||
| Enigmatic spiny-rayed fish from the Eocene of Monte Bolca, Italy | Q54555498 | ||
| A New Late Cretaceous Macrosemiid Fish (Neopterygii, Halecostomi) from Morocco, with Temporal and Geographical Range Extensions for the Family | Q54559300 | ||
| Four new basal acanthomorph fishes from the Late Cretaceous of Morocco | Q54559327 | ||
| Polazzodus, gen. nov., a new pycnodont fish from the Late Cretaceous of northeastern Italy | Q54636274 | ||
| Evolutionary history of the devilrays (Chondrichthyes: Myliobatiformes) from fossil and morphological inference | Q54650218 | ||
| A rare elasmobranch assemblage from the Valanginian (Lower Cretaceous) of southern France | Q54650232 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Actinopterygii | Q127282 |
| P304 | page(s) | 950-981 | |
| P577 | publication date | 2015-06-23 | |
| P1433 | published in | Biological Reviews | Q2500948 |
| P1476 | title | 'Fish' (Actinopterygii and Elasmobranchii) diversification patterns through deep time | |
| P478 | volume | 91 |
| Q90425923 | A bizarre Eocene dasyatoid batomorph (Elasmobranchii, Myliobatiformes) from the Bolca Lagerstätte (Italy) reveals a new, extinct body plan for stingrays |
| Q55129081 | A synoptic review of the Eocene (Ypresian) cartilaginous fishes (Chondrichthyes: Holocephali, Elasmobranchii) of the Bolca Konservat-Lagerstätte, Italy. |
| Q90240379 | Climate cooling and clade competition likely drove the decline of lamniform sharks |
| Q110667898 | Durnonovariaodus maiseyi gen. et sp. nov., a new hybodontiform shark-like chondrichthyan from the Upper Jurassic Kimmeridge Clay Formation of England |
| Q38738829 | Evolutionary bottlenecks in brackish water habitats drive the colonization of fresh water by stingrays. |
| Q98158706 | Evolutionary trends of the conserved neurocranium shape in angel sharks (Squatiniformes, Elasmobranchii) |
| Q54935953 | Exceptional preservation of a Cretaceous intestine provides a glimpse of the early ecological diversity of spiny-rayed fishes (Acanthomorpha, Teleostei). |
| Q28602865 | Extinction of fish-shaped marine reptiles associated with reduced evolutionary rates and global environmental volatility |
| Q110667485 | Guiclupea superstes, gen. et sp. nov., the youngest ellimmichthyiform (clupeomorph) fish to date from the Oligocene of South China |
| Q51212767 | Linking species habitat and past palaeoclimatic events to evolution of the teleost innate immune system. |
| Q28597314 | Little evidence for enhanced phenotypic evolution in early teleosts relative to their living fossil sister group |
| Q110668019 | Manta-like planktivorous sharks in Late Cretaceous oceans |
| Q116817011 | Morphology and paleobiology of the Late Cretaceous large-sized shark Cretodus crassidens (Dixon, 1850) (Neoselachii; Lamniformes) |
| Q64251903 | Netting the Stress Responses in Fish |
| Q33585188 | No evidence for the radiation time lag model after whole genome duplications in Teleostei |
| Q92638346 | On trends and patterns in macroevolution: Williston's law and the branchiostegal series of extant and extinct osteichthyans |
| Q51733194 | Phylogenetic analysis shows the general diversification pattern of deep-sea notacanthiforms (Teleostei: Elopomorpha). |
| Q57095387 | Revision of Eocene electric rays (Torpediniformes, Batomorphii) from the Bolca Konservat-Lagerstätte, Italy, reveals the first fossil embryo in marine batoids and provides new insights into the origin of trophic novelties in coral reef fishes |
| Q110668989 | Skeletal remains of the oldest known pseudocoracid shark Pseudocorax kindlimanni sp. nov. (Chondrichthyes, Lamniformes) from the Late Cretaceous of Lebanon |
| Q28818310 | Successive Losses of Central Immune Genes Characterize the Gadiformes' Alternate Immunity |
| Q36335297 | Testing for the Occurrence of Selective Episodes During the Divergence of Otophysan Fishes: Insights from Mitogenomics |
| Q54771059 | The first articulated specimen of the Cretaceous mackerel shark Haimirichia amonensis gen. nov. (Haimirichiidae fam. nov.) reveals a novel ecomorphological adaptation within the Lamniformes (Elasmobranchii) |
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