All Stories

  1. Symbiotic interactions in the Ordovician of Baltica
  2. Earliest known rugosan-stromatoporoid symbiosis from the Llandovery of Estonia (Baltica)
  3. Wenlock and Pridoli (Silurian) crinoids from Saaremaa, western Estonia (Phylum Echinodermata)
  4. Middle Jurassic (Callovian) cyclostome bryozoans from the Tethyan tropics (Matmor Formation, southern Israel)
  5. Bitten spines reveal unique evidence for fish predation on Middle Jurassic echinoids
  6. The earliest bryozoan parasite: Middle Ordovician (Darriwilian) of Osmussaar Island, Estonia
  7. Parasitism of a new apiocrinitid crinoid species from the Middle Jurassic (Callovian) of southern Israel
  8. Bivalve borings, bioclaustrations and symbiosis in corals from the Upper Cretaceous (Cenomanian) of southern Israel
  9. Earliest rhynchonelliform brachiopod parasite from the Late Ordovician of northern Estonia (Baltica)
  10. The Earliest Giant Osprioneides Borings from the Sandbian (Late Ordovician) of Estonia
  11. Symbiotic endobiont biofacies in the Silurian of Baltica
  12. SYMBIOTIC WORM ENDOBIONTS IN A STROMATOPOROID FROM THE RHUDDANIAN (EARLY SILURIAN) OF HIIUMAA, ESTONIA
  13. Microconchid-dominated cobbles from the Upper Devonian of Russia: Opportunism and dominance in a restricted environment following the Frasnian–Famennian biotic crisis
  14. Correlation of the Middle Jurassic (Callovian) Formations Across the Dead Sea Rift
  15. A Middle Ordovician crinoid from the beach gravels of Ristna Cape, Hiiumaa Island, Estonia
  16. Silurian cornulitids of Estonia (Baltica)
  17. Talexirhynchia, a new rhynchonellid genus from the Jurassic Ethiopian Province of Jordan
  18. Reinterpretation of the Cambrian ‘bryozoan’ Pywackia as an octocoral
  19. An event bed with abundant Skolithos burrows from the late Pridoli (Silurian) of Saaremaa (Estonia)
  20. Chondrichthyans from the Menuha Formation (Late Cretaceous: Santonian–Early Campanian) of the Makhtesh Ramon region, southern Israel
  21. New Tethyan Apiocrinitidae (Crinoidea, Articulata) From the Jurassic of Israel
  22. Crinoids from the Silurian of Western Estonia
  23. UNUSUAL TUBULAR FOSSILS ASSOCIATED WITH MICROBIAL CRUSTS FROM THE MIDDLE JURASSIC OF POLAND: AGGLUTINATED POLYCHAETE WORM TUBES?
  24. Palaeoecology, Preservation and Taxonomy of Encrusting Ctenostome Bryozoans Inhabiting Ammonite Body Chambers in the Late Cretaceous Pierre Shale of Wyoming and South Dakota, USA
  25. Origin, palaeoecology and stratigraphic significance of bored and encrusted concretions from the Upper Cretaceous (Santonian) of southern Israel
  26. Redescription and neotype designation of the Middle Devonian microconchid (Tentaculita) species ‘Spirorbis’ Angulatus Hall, 1861
  27. Jurassic Rhynchonellide Brachiopods from the Jordan Valley
  28. A New Microconchid Tubeworm from the Artinskian (Lower Permian) of Central Texas, USA
  29. Sea-level oscillations during the last interglacial highstand recorded by Bahamas corals
  30. Diverse sclerozoan assemblages encrusting large bivalve shells from the Callovian (Middle Jurassic) of southern Poland
  31. Middle Jurassic (Bathonian) encrusted oncoids from the Polish Jura, southern Poland
  32. Origin and paleoecology of Middle Jurassic hiatus concretions from Poland
  33. Sabellid-dominated shallow water calcareous polychaete tubeworm association from the equatorial Tethys Ocean (Matmor Formation, Middle Jurassic, Israel)
  34. Occurrence of Giant Borings ofOsprioneides kamptoin the Lower Silurian (Sheinwoodian) Stromatoporoids of Saaremaa, Estonia
  35. Endosymbiotic Cornulites in the Sheinwoodian (Early Silurian) stromatoporoids of Saaremaa, Estonia
  36. Bioerosion in an equatorial Middle Jurassic coral–sponge reef community (Callovian, Matmor Formation, southern Israel)
  37. A large coral reef in the Pennsylvanian of Ziyun County, Guizhou (South China): The substrate and initial colonization environment of reef-building corals
  38. Borings in Quartzite Surf Boulders from the Upper Cambrian Basal Deadwood Formation, Black Hills of South Dakota
  39. Early large borings in a hardground of Floian-Dapingian age (Early and Middle Ordovician) in northeastern Estonia (Baltica)
  40. Addition to the top of the stratigraphic column of the Be'er Sheva Formation (Jurassic, Callovian-Oxfordian) in Hamakhtesh Hagadol, Israel
  41. The Ramonalinids: a new family of mound-building bivalves of the Early Middle Triassic
  42. Paleoecology of a Pennsylvanian encrusting colonial rugose coral in south Guizhou, China
  43. A new equatorial, very shallow marine sclerozoan fauna from the Middle Jurassic (late Callovian) of southern Israel
  44. ORDOVICIAN BRYOZOANS FROM THE KANOSH FORMATION (WHITEROCKIAN) OF UTAH, USA
  45. Paleontological evidence of a brief global sea-level event during the last interglacial
  46. Macroborings and the Evolution of Marine Bioerosion
  47. Patterns and Processes in the Ordovician Bioerosion Revolution
  48. Predatory drill holes and partial mortality in Devonian colonial metazoans
  49. Predatory drill holes and partial mortality in Devonian colonial metazoans
  50. Development of a Jurassic rocky shore complex (Zohar Formation, Makhtesh Qatan, southern Israel)
  51. Calcite precipitation and dissolution of biogenic aragonite in shallow Ordovician calcite seas
  52. Palaeoecology and evolution of marine hard substrate communities
  53. A New Terminology for Marine Organisms Inhabiting Hard Substrates
  54. Edward Condon Remembered
  55. Palaeocology of Hard Substrate Faunas from the Cretaceous Qahlah Formation of the Oman Mountains
  56. Asteriacites lumbricalisvon schlotheim 1820: Ophiuroid trace fossils from the lower triassic thaynes formation, central Utah
  57. The first thecideide brachiopod from the Jurassic of North America
  58. a new ichnogenus for etchings made by cheilostome bryozoans into calcareous substrates
  59. Bahamian coral reefs yield evidence of a brief sea-level lowstand during the last interglacial: Reply
  60. Bahamian coral reefs yield evidence of a brief sea-level lowstand during the last interglacial
  61. Origin and Paleoecology of Free-Rolling Oyster Accumulations (Ostreoliths) in the Middle Jurassic of Southwestern Utah, USA
  62. Succession in a Jurassic marine cavity community and the evolution of cryptic marine faunas
  63. Paleoenvironmental and paleoecologic analyses of a Pleistocene mollusc-rich lagoonal facies, San Salvador Island, Bahamas
  64. Earliest preservation of soft-bodied fossils by epibiont bioimmuration: Upper Ordovician of Kentucky
  65. A carbonate hardground in the carmel formation (middle jurassic, sw utah, usa) and its associated encrusters, borers and nestlers
  66. Fossils in the Field
  67. The development of an Early Ordovician hard ground community in response to rapid sea-floor calcite precipitation
  68. Growth of ferruginous oncoliths in the Bajocian (Middle Jurassic) of Europe
  69. Paleoecology of Sphenothallus on an Upper Ordovician hardground
  70. Ecological Dynamics on Pebbles, Cobbles, and Boulders
  71. Disturbance and Ecologic Succession in an Upper Ordovician Cobble-Dwelling Hardground Fauna
  72. Origin of brachiopod-bryozoan assemblages in an Upper Carboniferous limestone: importance of physical and ecological controls