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GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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Africa
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Madagascar (1)
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North Africa
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Atlas Mountains
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Moroccan Atlas Mountains
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Anti-Atlas (2)
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Egypt (2)
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Morocco
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Moroccan Atlas Mountains
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Anti-Atlas (2)
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Tafilalt (1)
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-
-
Southern Africa
-
Namibia (1)
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South Africa
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Western Cape Province South Africa (1)
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-
-
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Antarctica
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Antarctic Peninsula (1)
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Arctic Ocean
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Barents Sea (1)
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Arctic region
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Greenland
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East Greenland (1)
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Jameson Land (1)
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Asia
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Arabian Peninsula
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Saudi Arabia (2)
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Far East
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Burma (1)
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China
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Indian Peninsula
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India (1)
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Middle East
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Sri Lanka (1)
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Atlantic Ocean
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Australasia
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Canada
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Newfoundland and Labrador
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Ontario
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Commonwealth of Independent States
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Southern Europe
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Indian Ocean
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commodities
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oil and gas fields (1)
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elements, isotopes
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carbon
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C-13 (1)
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C-13/C-12 (1)
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isotope ratios (2)
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isotopes
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stable isotopes
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C-13 (1)
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C-13/C-12 (1)
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metals
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alkaline earth metals
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calcium (1)
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molybdenum (1)
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nitrogen (1)
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oxygen (1)
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sulfur (1)
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fossils
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borings (4)
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burrows (15)
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Chordata
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Vertebrata
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Agnatha
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Heterostraci (1)
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Pisces
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Chondrichthyes (1)
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Osteichthyes
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Sarcopterygii
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Crossopterygii (1)
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Tetrapoda
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Reptilia
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Anapsida
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Testudines
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Cryptodira (1)
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Emydidae (1)
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Diapsida
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Archosauria
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dinosaurs (1)
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Pterosauria (1)
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cyanobacteria (1)
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Cyclostomata (1)
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Graptolithina
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Hemichordata (2)
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ichnofossils
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Ophiomorpha (1)
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Planolites (1)
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Skolithos (2)
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Teichichnus (1)
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Thalassinoides (2)
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Trypanites (1)
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Invertebrata
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Arthropoda
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Chelicerata
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Arachnida (1)
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Merostomata
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Eurypterida (1)
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Mandibulata
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Crustacea
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Branchiopoda (1)
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Cirripedia (1)
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Copepoda (1)
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Malacostraca
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Callianassa (1)
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Ostracoda
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Podocopida
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Cypridocopina (1)
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Insecta
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Pterygota
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Neoptera
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Endopterygota
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Diptera (1)
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Exopterygota
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Hemiptera (1)
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Orthoptera (1)
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Myriapoda (1)
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Trilobitomorpha
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Trilobita (10)
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Brachiopoda
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Articulata
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Orthida (1)
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Spiriferida (1)
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Inarticulata (1)
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Bryozoa (9)
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Cnidaria
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Anthozoa
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Zoantharia
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Scleractinia (1)
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Tabulata (1)
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Hydrozoa (4)
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Echinodermata
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Crinozoa
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Crinoidea (5)
-
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Echinozoa
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Holothuroidea (4)
-
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Homalozoa
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Machaeridia (3)
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-
-
Mollusca
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Bivalvia
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Heterodonta
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Veneroida
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Lucinidae (1)
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Vesicomyidae (1)
-
-
-
-
Cephalopoda
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Ammonoidea
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Baculites (1)
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Nautiloidea (2)
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Gastropoda
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Mesogastropoda (1)
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Polyplacophora (1)
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Scaphopoda (2)
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Porifera
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Demospongea (1)
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Protista
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Foraminifera
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Fusulinina
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Fusulinidae (1)
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Rotaliina
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Buliminacea
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Uvigerinidae
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Uvigerina
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Uvigerina peregrina (1)
-
-
-
-
-
-
Radiolaria (3)
-
-
Vermes
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Annelida
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Chaetopoda (1)
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Chaetognatha (1)
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Nematoida (1)
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Polychaeta
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Serpulidae (8)
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Priapulida (2)
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scolecodonts (14)
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-
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Metazoa (3)
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microfossils
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Chitinozoa (2)
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Conodonta (9)
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Fusulinina
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Fusulinidae (1)
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scolecodonts (14)
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palynomorphs
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acritarchs (3)
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Chitinozoa (2)
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Dinoflagellata (4)
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miospores
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pollen (1)
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Plantae
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algae
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Chlorophyta (1)
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Coccolithophoraceae (2)
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diatoms (2)
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nannofossils (2)
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Rhodophyta (1)
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Pteridophyta
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Lycopsida (1)
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Sphenopsida
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Equisetales
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Calamites (1)
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Spermatophyta
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Angiospermae (1)
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Gymnospermae
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Cordaitales (1)
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Ginkgoales (1)
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Pteridospermae (1)
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problematic fossils (7)
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Pterobranchia (2)
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thallophytes (3)
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trails (2)
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geologic age
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Cenozoic
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Quaternary
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Holocene
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upper Holocene (1)
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Pleistocene (2)
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Tertiary
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Neogene
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Miocene
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upper Miocene
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Messinian
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Pliocene (1)
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Paleogene
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Eocene
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lower Eocene
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Ypresian (1)
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upper Eocene (1)
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Oligocene (1)
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Paleocene
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Midway Group (1)
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-
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Mesozoic
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Cretaceous
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Dakota Formation (1)
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Graneros Shale (1)
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Lower Cretaceous
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Albian (1)
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Middle Cretaceous (1)
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Upper Cretaceous
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Cenomanian
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upper Cenomanian (1)
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Greenhorn Limestone (1)
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Pierre Shale (1)
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Senonian (1)
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Turonian
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upper Turonian (1)
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Jurassic
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Lower Jurassic
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Triassic-Jurassic boundary (1)
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Upper Jurassic
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Oxfordian (1)
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Triassic
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Lower Triassic
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Griesbachian (1)
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Permian-Triassic boundary (2)
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Montney Formation (1)
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Upper Triassic
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Triassic-Jurassic boundary (1)
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-
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Paleozoic
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Cambrian
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Lower Cambrian
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Poleta Formation (1)
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Middle Cambrian
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Burgess Shale (1)
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Upper Cambrian (1)
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Carboniferous
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Mississippian
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Windsor Group (1)
-
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Pennsylvanian
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Cumberland Group (1)
-
Francis Creek Shale (2)
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Joggins Formation (1)
-
Middle Pennsylvanian
-
Carbondale Formation (1)
-
-
Upper Pennsylvanian
-
Virgilian (1)
-
-
-
-
Deadwood Formation (1)
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Devonian
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Genesee Group (1)
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Lower Devonian
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Siegenian (1)
-
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Middle Devonian
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Eifelian (1)
-
-
Traverse Group (1)
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Upper Devonian
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Famennian (1)
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Ohio Shale (1)
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-
-
lower Paleozoic
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Cape Phillips Formation (1)
-
-
Ordovician
-
Lower Ordovician
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Tremadocian (1)
-
-
Middle Ordovician
-
Decorah Shale (1)
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Normanskill Formation (1)
-
-
Trenton Group (2)
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Upper Ordovician
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Caradocian (1)
-
Cincinnatian
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Richmondian (1)
-
-
Fairview Formation (1)
-
Hirnantian (1)
-
Kope Formation (2)
-
Trentonian (2)
-
Whitewater Formation (1)
-
-
Viola Limestone (1)
-
-
Permian
-
Khuff Formation (1)
-
Upper Permian
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Cadeby Formation (1)
-
Lopingian (1)
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Permian-Triassic boundary (2)
-
Zechstein (1)
-
-
-
Silurian
-
Lower Silurian
-
Llandovery
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Aeronian (1)
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Telychian (3)
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Wenlock (1)
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Upper Silurian (1)
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upper Paleozoic (1)
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-
Precambrian
-
upper Precambrian
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Proterozoic
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Neoproterozoic
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Ediacaran (3)
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-
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igneous rocks
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igneous rocks (1)
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metamorphic rocks
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turbidite (1)
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minerals
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carbonates
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dolomite (1)
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magnesian calcite (1)
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siderite (1)
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organic minerals
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amber (1)
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silicates
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sheet silicates
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clay minerals
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kaolinite (1)
-
-
serpentine group
-
berthierine (1)
-
-
-
-
sulfides
-
pyrite (1)
-
-
-
Primary terms
-
Africa
-
Madagascar (1)
-
North Africa
-
Atlas Mountains
-
Moroccan Atlas Mountains
-
Anti-Atlas (2)
-
-
-
Egypt (2)
-
Morocco
-
Moroccan Atlas Mountains
-
Anti-Atlas (2)
-
-
Tafilalt (1)
-
-
-
Southern Africa
-
Namibia (1)
-
South Africa
-
Western Cape Province South Africa (1)
-
-
-
-
Antarctica
-
Antarctic Peninsula (1)
-
-
Arctic Ocean
-
Barents Sea (1)
-
-
Arctic region
-
Greenland
-
East Greenland (1)
-
Jameson Land (1)
-
-
-
Asia
-
Arabian Peninsula
-
Saudi Arabia (2)
-
United Arab Emirates
-
Abu Dhabi (1)
-
-
-
Far East
-
Burma (1)
-
China
-
Shandong China
-
Huang He delta (1)
-
-
-
-
Indian Peninsula
-
Godavari River (1)
-
India (1)
-
-
Middle East
-
Cyprus (1)
-
Lebanon (1)
-
-
Sri Lanka (1)
-
-
Atlantic Ocean
-
North Atlantic
-
Bay of Fundy (1)
-
Gulf of Mexico (2)
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Gulf of Saint Lawrence (1)
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Irish Sea (1)
-
-
-
Australasia
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Australia (1)
-
-
bibliography (5)
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biogeography (6)
-
Canada
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Eastern Canada
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Maritime Provinces
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Nova Scotia
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Minas Basin (1)
-
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Newfoundland and Labrador
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Newfoundland
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Burin Peninsula (1)
-
-
-
Ontario
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Bruce County Ontario (1)
-
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Quebec
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Gaspe-Est County Quebec
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Gaspe Quebec (1)
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Quebec City Quebec (1)
-
-
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Western Canada
-
Alberta (2)
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British Columbia (4)
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Northwest Territories (1)
-
-
-
carbon
-
C-13 (1)
-
C-13/C-12 (1)
-
-
Caribbean region
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West Indies
-
Antilles
-
Greater Antilles
-
Hispaniola
-
Dominican Republic (1)
-
-
-
Lesser Antilles
-
Trinidad and Tobago
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Trinidad (1)
-
-
-
-
-
-
Cenozoic
-
Quaternary
-
Holocene
-
upper Holocene (1)
-
-
Pleistocene (2)
-
-
Tertiary
-
Neogene
-
Miocene
-
lower Miocene (1)
-
upper Miocene
-
Messinian
-
Messinian Salinity Crisis (1)
-
-
-
-
Pliocene (1)
-
-
Paleogene
-
Eocene
-
lower Eocene
-
Ypresian (1)
-
-
upper Eocene (1)
-
-
Oligocene (1)
-
Paleocene
-
Midway Group (1)
-
-
-
-
-
Chordata
-
Vertebrata
-
Agnatha
-
Heterostraci (1)
-
-
Pisces
-
Chondrichthyes (1)
-
Osteichthyes
-
Sarcopterygii
-
Crossopterygii (1)
-
-
-
-
Tetrapoda
-
Reptilia
-
Anapsida
-
Testudines
-
Cryptodira (1)
-
Emydidae (1)
-
-
-
Diapsida
-
Archosauria
-
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GeoRef Categories
Era and Period
Epoch and Age
Book Series
Date
Availability
Annelida
Exceptionally preserved burrows of ichnogenus Asterosoma from the lower Silurian of south China: systematic ichnology, palaeoecology and implications for ecosystem recovery following the late Ordovician mass extinction
NEOICHNOLOGY OF A MICROTIDAL CARBONATE INTERTIDAL ZONE: ABU DHABI, U.A.E.
Cryophilic polychaetes at the subtropical Laurentian margin of the Iapetus Ocean: Evidence for cold-water ocean circulation and upwelling
The famous fish beds of Lebanon: the Upper Cretaceous Lagerstätten of Haqel, Hjoula, Nammoura and Sahel Aalma
HYBRID NATURE OF A NEW JURASSIC–CRETACEOUS WORM BURROW INDICATED BY MICROBIAL MEDIATION OF ITS WALL FORMATION
HELMINTHOPSIS AND CYLINDRICHNUS ICHNOGUILDS FROM MIOCENE THIN-BEDDED TURBIDITES, TIERRA DEL FUEGO, ARGENTINA
Molybdenum isotope signature of microbial nitrogen utilization in siboglinid tubeworms
Aspects of Aktuo-Paläontologie of the rocky beaches of the eastern Isle of Mull, UK
Abstract Owing to the increasing availability of data for many fossil groups and a generally accepted palaeogeographical configuration, palaeontologists have been able to develop progressively more robust palaeobiogeographical scenarios for the spatial distributions of Ordovician marine faunas. However, most research in Early Paleozoic palaeobiogeography centres on data derived from extensively studied localities in North America and Europe. Thus, clear patterns are emerging of regional biogeography for these areas. However, the fragmentary nature of data from other regions hinders the development of a detailed understanding of palaeogeographical schemes of many clades at the global level. Provincial patterns are now available for several fossil groups, but the global coverage remains generally fragmentary. Palaeobiogeographical investigations were traditionally focused on better understanding of palaeogeographical scenarios and often employed quantitative analyses of faunal similarity. More recently palaeobiogeographical analyses have expanded to investigate questions such as the location and pace of speciation and macroevolution together with macroecological change. For example, studies on the evolution of speciation levels in the frame of the taxonomic radiation of the Great Ordovician Biodiversification are now available. Future investigations, including modelling, will provide more integrative, global patterns of provincialism, including the location of Ordovician biodiversity hotspots and the recognition of latitudinal diversity gradients.
Messinian seep-carbonates marking the transition to the evaporite deposits in the Romagna sector of the northern Apennines (Italy)
THE OCCURRENCE OF BONE MODIFICATION FEATURES IN THE CARAPACE AND PLASTRON OF THE EXTANT RED-EARED SLIDER TRACHEMYS SCRIPTA ELEGANS (WIED-NEUWIED, 1839): IMPLICATIONS FOR PALEOECOLOGICAL ANALYSES OF FOSSIL TURTLE ASSEMBLAGES
Machine learning identifies ecological selectivity patterns across the end-Permian mass extinction
The Late Ordovician Tafilalt Biota, Anti-Atlas, Morocco: a high-latitude perspective on the GOBE
Abstract The extensive, predominantly siliciclastic deposits of the Upper Ordovician of the Tafilalt have long been the subject of scientific investigation. In the past 25 years, intensified collecting for commercial purposes has resulted in the discovery of several exceptionally-preserved faunas (Konservat-Lagerstätten) in the Tafilalt region, preserving a range of non-biomineralized and soft-bodied organisms. The preservation of these fossils in the coarse clastic sediments of the Tafilalt is surprising, and in the case of soft-bodied organisms, remarkably similar to the preservational mode of typical Ediacaran biotas. These relatively recent discoveries have increased the scientific significance of the Tafilalt Biota, providing an unparalleled insight into the composition and temporal evolution of the shallow, open-marine ecosystems and their denizens during the later stages of the Great Ordovician Biodiversification Event. At least nine different phyla, in addition to several soft-bodied problematica are represented in the Tafilalt. While the highly diverse and remarkably well-preserved echinoderm and euarthropod faunas are most emblematic for the Tafilalt Biota, further studies have revealed a relatively high diversity of molluscs and brachiopods. Among soft-bodied fossils, the problematic paropsonemid eldonids are iconic for the Tafilalt and stand out both through their abundance, and their wide temporal and geographical range throughout the area.
Distribution and correlation of Sabellidites cambriensis (Annelida?) in the basal Cambrian on Baltica
The trace fossil Polykampton recurvum n. isp. (sequestrichnia) from the Maastrichtian–Paleocene deep-sea deposits of NW Italy
Abstract Nine non-pollen palynomorph (NPP) groups occur in Quaternary marine and brackish-water sediments; these groups represent various planktonic or micro- to macrobenthic organisms. Some extant NPP were previously classified as fossil Acritarcha, Chitinozoa or scolecodonts. We refer to reviews of these fossils and their applications for Paleozoic–Mesozoic biostratigraphy and palaeoecology but focus on extant marine NPP that can be studied by laboratory culture, genetics or micro-geochemical methods. Marine NPP include resting cysts of planktonic dinoflagellates and prasinophytes, tintinnids and other cilates, copepod eggs and skeletal remains, and various microzoobenthos: microforaminiferal organic linings, ostracod mandibles and carapace linings, various worm egg capsules and mouthparts. New micro-Fourier Transform Infrared spectroscopy spectra suggest the probable affinities of the tintinnid cyst type P and Beringiella . Our applications in marine biodiversity and provincialism studies emphasize under-studied polar regions and neglected ice-algae nano-plankton and compare climate-based NPP distributions to Ocean Biogeographic Information System realms. Trophic relationships are outlined using sediment-trap studies. Seasonal to annual-scale investigations of palaeoproduction provide new perspectives on ocean carbon budgets during times of rapid climate change and atmospheric carbon increase. More taxonomic and source-linkage studies of non-dinocyst marine NPP are needed but we outline potentials for studies of hemispheric or global-scale shifts in marine food webs as driven by ocean warming.