- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
- Abstract
- Affiliation
- All
- Authors
- Book Series
- DOI
- EISBN
- EISSN
- Full Text
- GeoRef ID
- ISBN
- ISSN
- Issue
- Keyword (GeoRef Descriptor)
- Meeting Information
- Report #
- Title
- Volume
NARROW
GeoRef Subject
-
all geography including DSDP/ODP Sites and Legs
-
Africa
-
Madagascar (1)
-
North Africa
-
Morocco (1)
-
-
Southern Africa
-
Namibia (2)
-
-
-
Asia
-
Far East
-
China (1)
-
Philippine Islands (1)
-
-
-
Canada
-
Western Canada
-
Saskatchewan (1)
-
-
-
Europe
-
Central Europe
-
Germany (1)
-
-
-
Indian Ocean Islands
-
Madagascar (1)
-
-
North America
-
Western Interior (1)
-
-
United States
-
Alaska (1)
-
New York (1)
-
North Carolina (1)
-
South Dakota
-
Moody County South Dakota (1)
-
-
Washington (1)
-
Wisconsin
-
Marathon County Wisconsin (1)
-
-
-
-
fossils
-
bacteria (1)
-
burrows (2)
-
Chordata
-
Vertebrata
-
Tetrapoda
-
Mammalia
-
Theria
-
Eutheria
-
Cetacea (1)
-
-
-
-
Reptilia
-
Diapsida
-
Lepidosauria
-
Squamata
-
Lacertilia
-
Mosasauridae (1)
-
-
-
-
-
-
-
-
-
Cloudina (1)
-
coprolites (1)
-
Hemichordata (1)
-
ichnofossils (4)
-
Invertebrata
-
Arthropoda
-
Chelicerata (1)
-
Mandibulata
-
Crustacea
-
Cirripedia (1)
-
-
-
-
Cnidaria (1)
-
Echinodermata
-
Asterozoa
-
Stelleroidea
-
Asteroidea (1)
-
-
-
Crinozoa
-
Crinoidea (3)
-
-
-
Mollusca
-
Bivalvia (1)
-
Cephalopoda
-
Ammonoidea (2)
-
Nautiloidea
-
Nautilus (1)
-
-
-
Gastropoda (1)
-
-
-
Metazoa (1)
-
problematic fossils (2)
-
tracks (1)
-
-
geologic age
-
Cenozoic
-
Tertiary
-
Neogene
-
Miocene
-
upper Miocene (1)
-
-
-
Paleogene
-
Eocene (2)
-
-
-
-
Mesozoic
-
Cretaceous
-
Upper Cretaceous
-
Bearpaw Formation (1)
-
Pierre Shale (1)
-
-
-
Jurassic (1)
-
-
Paleozoic
-
Cambrian
-
Lower Cambrian (2)
-
Upper Cambrian (1)
-
-
Devonian (2)
-
Permian (1)
-
Silurian (1)
-
-
Precambrian
-
upper Precambrian
-
Proterozoic
-
Neoproterozoic
-
Ediacaran (3)
-
Vendian (4)
-
-
-
-
-
-
minerals
-
carbonates
-
siderite (1)
-
-
-
Primary terms
-
Africa
-
Madagascar (1)
-
North Africa
-
Morocco (1)
-
-
Southern Africa
-
Namibia (2)
-
-
-
Asia
-
Far East
-
China (1)
-
Philippine Islands (1)
-
-
-
bacteria (1)
-
Canada
-
Western Canada
-
Saskatchewan (1)
-
-
-
Cenozoic
-
Tertiary
-
Neogene
-
Miocene
-
upper Miocene (1)
-
-
-
Paleogene
-
Eocene (2)
-
-
-
-
Chordata
-
Vertebrata
-
Tetrapoda
-
Mammalia
-
Theria
-
Eutheria
-
Cetacea (1)
-
-
-
-
Reptilia
-
Diapsida
-
Lepidosauria
-
Squamata
-
Lacertilia
-
Mosasauridae (1)
-
-
-
-
-
-
-
-
-
coprolites (1)
-
data processing (1)
-
deformation (1)
-
diagenesis (1)
-
Europe
-
Central Europe
-
Germany (1)
-
-
-
Hemichordata (1)
-
ichnofossils (4)
-
Indian Ocean Islands
-
Madagascar (1)
-
-
Invertebrata
-
Arthropoda
-
Chelicerata (1)
-
Mandibulata
-
Crustacea
-
Cirripedia (1)
-
-
-
-
Cnidaria (1)
-
Echinodermata
-
Asterozoa
-
Stelleroidea
-
Asteroidea (1)
-
-
-
Crinozoa
-
Crinoidea (3)
-
-
-
Mollusca
-
Bivalvia (1)
-
Cephalopoda
-
Ammonoidea (2)
-
Nautiloidea
-
Nautilus (1)
-
-
-
Gastropoda (1)
-
-
-
Mesozoic
-
Cretaceous
-
Upper Cretaceous
-
Bearpaw Formation (1)
-
Pierre Shale (1)
-
-
-
Jurassic (1)
-
-
North America
-
Western Interior (1)
-
-
paleoecology (6)
-
paleogeography (1)
-
paleontology (1)
-
Paleozoic
-
Cambrian
-
Lower Cambrian (2)
-
Upper Cambrian (1)
-
-
Devonian (2)
-
Permian (1)
-
Silurian (1)
-
-
Precambrian
-
upper Precambrian
-
Proterozoic
-
Neoproterozoic
-
Ediacaran (3)
-
Vendian (4)
-
-
-
-
-
problematic fossils (2)
-
sedimentary rocks
-
clastic rocks
-
sandstone (1)
-
-
-
sedimentary structures
-
biogenic structures
-
algal structures
-
algal mats (1)
-
-
-
-
sedimentation (1)
-
United States
-
Alaska (1)
-
New York (1)
-
North Carolina (1)
-
South Dakota
-
Moody County South Dakota (1)
-
-
Washington (1)
-
Wisconsin
-
Marathon County Wisconsin (1)
-
-
-
-
rock formations
-
Nama Group (2)
-
-
sedimentary rocks
-
sedimentary rocks
-
clastic rocks
-
sandstone (1)
-
-
-
-
sedimentary structures
-
burrows (2)
-
coprolites (1)
-
sedimentary structures
-
biogenic structures
-
algal structures
-
algal mats (1)
-
-
-
-
tracks (1)
-
EARLY MOLLUSCAN EVOLUTION: EVIDENCE FROM THE TRACE FOSSIL RECORD
Hermit arthropods 500 million years ago?
Abstract: Invertebrate trace fossils are usually considered as stratigraphically less useful than vertebrate footprints. This is because they commonly lack diagnostic “fingerprints”, which are more closely related to the anatomy of the producer than to the biological purpose, or function, of the trace. Exceptions are trilobite burrows (Cruziana) , arthrophycid burrows, ichnospecies of Oldhamia, and Treptichnus pedum. Even if their makers are unknown, they represent taxonomically coherent groups of animals, whose evolving behavior marks geologic time. Cruziana ichnospecies can also be used in paleogeography.
CRINOID ANCHORING STRATEGIES FOR SOFT-BOTTOM DWELLING (SEILACHER AND MACCLINTOCK, 2005)
A re-examination of the Nama-type Vendian organism Rangea schneiderhoehni
Crinoid Anchoring Strategies for Soft-Bottom Dwelling
Whale barnacles: exaptational access to a forbidden paradise
Constructional Morphology of Pelagic Crinoids
A fresh look at sideritic “coprolites”
Precambrian “fossil” Vermiforma is a tectograph
Biomat-related lifestyles in the Precambrian
Alleged mosasaur bite marks on Late Cretaceous ammonites are limpet (patellogastropod) home scars
The Phylum Vendobionta; a sister group of the Eumetazoa?
Spirocosmorhaphe, a new graphoglyptid trace fossil
Pattern recognition problems in geology and paleontology
Constructional morphology of sand dollars
Use of Trace Fossil Assemblages for Recognizing Depositional Environments
Abstract For environmental interpretation, biogenic sedimentary structures have the obvious advantage that they are absolutely autochthonous (rare exceptions can be easily recognized) and that they reflect a direct behavioral response to environmental conditions. On the other hand, the palichnological record is largely biased by preservational factors. The majority of the biogenic traces that we observe in present-day environments, particularly the exichnial ones--those on the upper surface of a bed (Martinsson, 1970; Chapter 1 , Table 2) -- may have an almost zero fossilization potential. We, therefore, consider the study of modern traces as a prerequisite to understanding the origin of individual trace fossils, but our paleoenvironmental classification is based mainly on comparisons between fossil ichnocoenoses; i.e., on the other side of the “f ossilizati barrier”.