| The middle Miocene palynofloras of the Salihpasalar lignite mine (Yatagan Basin, southwest Anatolia): environmental characterisation and comparison with palynofloras from adjacent basins |
5 |
| Palaeoenvironmental change across the Permian-Triassic boundary inferred from palynomorph assemblages (Godavari Graben, south India) |
5 |
| Conodont biostratigraphy of the Kesheh and Dizlu sections, and the age range of the Bahram Formation in central Iran |
5 |
| Cuticle surfaces of fossil plants as a potential proxy for volcanic SO2 emissions: observations from the Triassic-Jurassic transition of East Greenland |
4 |
| Rodent faunas from the Paleogene of south-east Serbia |
4 |
| On a new diatomyid (Rodentia, Mammalia) from the Paleogene of south-east Serbia, the first record of the family in Europe |
4 |
| New Melissiodontinae (Mammalia, Rodentia) from the Paleogene of south-east Serbia |
4 |
| Reconciling the stratigraphy and depositional history of the Lycian orogen-top basins, SW Anatolia |
3 |
| Fire in the paradise: evidence of repeated palaeo-wildfires from the Araripe Fossil Lagerstatte (Araripe Basin, Aptian-Albian), Northeast Brazil |
3 |
| A unique middle Miocene (Sarmatian) fish fauna from coastal deposits in the eastern Pannonian Basin (Romania) |
3 |
| Pappocricetodontinae (Rodentia, Muridae) from the Paleogene of south-east Serbia |
3 |
| Tetrapod diversity and palaeoecology in the German Middle Triassic (Lower Keuper) documented by tooth morphotypes |
3 |
| Lower Miocene alligatoroids (Crocodylia) from the Castillo Formation, northwest of Venezuela |
3 |
| Ostracods from the Devonian-Carboniferous transition in Dushan of Guizhou, South China |
2 |
| Fires and storms-a Triassic-Jurassic transition section in the Sichuan Basin, China |
2 |
| Palaeovegetational evolution of the cankiri-corum Basin during the Mio-Pliocene (Central Anatolia) based on the IPR analysis method |
2 |
| Fossil burrow assemblage, not mangrove roots: reinterpretation of the main whale-bearing layer in the late Eocene of Wadi Al-Hitan, Egypt |
2 |
| Conodont stratigraphy and conodont biofacies of the shallow-water Kuh-e-Bande-Abdol-Hossein section (SE Anarak, Central Iran) |
2 |
| Land or water: using taphonomic models to determine the lifestyle of the Triassic protorosaur Tanystropheus (Diapsida, Archosauromorpha) |
2 |
| Foraminiferal palaeobathymetry and depositional sequences of the subsurface Eocene Apollonia Formation in North Western Desert, Egypt |
2 |
| Paracricetodontinae (Mammalia, Rodentia) from the late Eocene and early Oligocene of south-east Serbia |
2 |
| A new carnivoran fauna from the late Oligocene of Hungary |
1 |
| Litho bio and sequence stratigraphy of the Boyle-Portwood Succession (Middle Devonian, Central Kentucky, USA) |
1 |
| Biochronological and palaeobiogeographical significance of the earliest Miocene mammal fauna from Northern Vietnam |
1 |
| First record of Eocene fossil rodent assemblages from the lower part of the Erden Obo Section, Erlian Basin (Nei Mongol, China) and its biochronological implications |
1 |
| Applications of species distribution modeling for palaeontological fossil detection: late Pleistocene models of Saiga (Artiodactyla: Bovidae, Saiga tatarica) |
1 |
| A remarkable mass-assemblage of lycopsid remains from the Rio Bonito Formation, lower Permian of the Parana Basin, Rio Grande do Sul, Brazil |
1 |
| Palaeoecology of Late Carboniferous encrusting chaetetids in North China |
1 |
| New data on the anatomy and palaeobiology of sandcoleid mousebirds (Aves, Coliiformes) from the early Eocene of Messel |
1 |
| Joint vegetation and mammalian records at the early Pleistocene sequence of Bovila Ordis (Banyoles-Besalu Basin, NE Spain) and their bearing on early hominin occupation in Europe |
1 |
| Record of the Miocene Climate Optimum in the northeast Indian Ocean: evidence from the microfossils |
1 |
| New Latonia (Amphibia: Alytidae) from the late Miocene of northern Caucasus (Russia) |
1 |
| Givetian-Frasnian arid palaeoenvironments from the northern Gondwana: a case study from the Moesian platform (Bulgaria) |
1 |
| An interim global bioregionalisation of Devonian areas |
1 |
| Floral diversity and environment during the middle Siwalik sedimentation (Pliocene) in the Arunachal sub-Himalaya |
1 |
| Colony growth strategies, dormancy and repair in some Late Cretaceous encrusting bryozoans: insights into the ecology of the Chalk seabed |
1 |
| Middle Jurassic palaeoenvironment and palaeobiogeography of the Tabas Block, Central Iran: palynological and palaeobotanical investigations |
1 |
| Early Miocene insectivores of Gokler (Kazan Basin, Central Anatolia, Turkey) |
1 |
| A palaeoenvironmental reconstruction of the Middle Jurassic of Sardinia (Italy) based on integrated palaeobotanical, palynological and lithofacies data assessment |
1 |
| Hangenberg Black Shale with cymaclymeniid ammonoids in the terminal Devonian of South China |
1 |
| Permineralized osmundaceous and gleicheniaceous ferns from the Jurassic of Inner Mongolia, NE China |
1 |
| Emsian (Lower Devonian) conodonts from the Lufengshan section (Guangxi, South China) |
1 |
| The Triassic to Early Jurassic palynological record of the Tarim Basin, China |
1 |
| Megaspores from the Lower Jurassic (Pliensbachian) Rotzo Formation (Monti Lessini, northern Italy) and their palaeoenvironmental implications |
0 |
| The diversity of Australian Mesozoic bennettitopsid reproductive organs |
0 |
| New data on the biostratigraphy of the Early Devonian Spirifer tonkinensis brachiopod fauna in South China and adjacent region |
0 |
| Palaeobiogeographic dynamics of brachiopod faunas during the Frasnian-Famennian biotic crisis in South China |
0 |
| Morphometrics and palaeoecology of syringoporoid tabulate corals from the upper Famennian (Devonian) Etoucun Formation, Huilong, South China |
0 |
| Origination and diversification of Devonian ambocoelioid brachiopods in South China |
0 |
| Tentaculitids and their evolutionary significance in the Early Devonian Dashatian section, South China |
0 |
