Lower and Early Middle Cambrian Formations near Mount Robson, British Columbia and Alberta

1975 ◽  
Vol 12 (2) ◽  
pp. 119-131 ◽  
Author(s):  
W. H. Fritz ◽  
E. W. Mountjoy
Keyword(s):  
British Columbia ◽  
Lower Cambrian ◽  
Middle Cambrian ◽  
Physical Evidence ◽  
Control Section ◽  
Middle Unit

Five formations and part of a sixth were examined in order to resolve conflicting reports as to their age and lateral relationship. The formations are redescribed at their type sections and equivalent strata are described at a control section. It is concluded that the Lower Cambrian Mural, Mahto, and Hota Formations and the Middle Cambrian Chetang Formation are valid and that the Tah (= Mural) and Adolphus (= Hota) Formations should be suppressed. The boundary between the Nevadella and Bonnia-Olenellus Zone falls within the middle unit of the Mural. The Lower – Middle Cambrian boundary is located at or very near the contact between the Hota and overlying Chetang Formation. This is a sharp lithologic contract, but no physical evidence of an unconformity was noted.

Lower Cambrian pediculate lingulids from Yunnan, China

1993 ◽  
Vol 67 (5) ◽  
pp. 788-798 ◽  
Author(s):  
Jin Yugan ◽  
Hou Xianguang ◽  
Wang Huayu
Keyword(s):  
New York ◽  
British Columbia ◽  
Lower Cambrian ◽  
Structure And Function ◽  
The Other ◽  
Burgess Shale ◽  
Middle Cambrian ◽  
Middle Ordovician ◽  
Early Ordovician ◽  
And Function

The vermiform pedicle is one of the most distinctive organs of modern lingulids, but it is rarely preserved. Only two fossil specimens of lingulids with pedicle casts have been reported, one from the Ordovician and the other from the Devonian. No record of fossil pedicles of Lingulella and Lingulepis, the dominant Cambrian and Early Ordovician lingulids, is known. Fossil lingulids from the Lower Cambrian of Chengjiang County, Yunnan, suggest that the structure and function of the pedicle of the lingulids has not changed significantly from its first appearance. A comparison of fossil pedicle of lingulids from the Lower Cambrian, Chengjiang County (China), the Burgess Shale, Middle Cambrian, British Columbia (Canada), the Trenton Formation, Middle Ordovician, New York (U.S.A.), and the Devonian, Devonshire (England, U.K.) shows that the delthyrial area to which the pedicle muscles are attached was reduced in length through time until these muscles were completely embraced by the two valves.Two species, Lingulella chengjiangensis n. sp. and Lingulepis malongensis Rong, are described.

Cambrian Lagerstätten: their distribution and significance

1985 ◽  
Vol 311 (1148) ◽  
pp. 49-65 ◽  
Keyword(s):  
British Columbia ◽  
Special Reference ◽  
Community Ecology ◽  
Lower Cambrian ◽  
South Australia ◽  
Burgess Shale ◽  
Middle Cambrian ◽  
Upper Cambrian ◽  
Exceptional Preservation ◽  
Biotic Diversity

The geological setting, biotic diversity and taphonomy of Cambrian soft-bodied Lagerstätten are reviewed with special reference to the Lower Cambrian Emu Bay Shale (South Australia) and Kinzers Formation (Pennsylvania), and the Middle Cambrian Stephen Formation (Burgess Shale and adjacent localities, British Columbia). Brief mention is made also of a number of more minor occurrences in the U.S.A., China and Spain. Exceptional preservation in the Upper Cambrian is discussed by K. J. Müller (this symposium). These soft-bodied Lagerstätten afford a series of special insights into the nature of Cambrian life. Emphasis is laid on the information they provide with regards (i) levels of diversity and the proportion of skeletized taxa; (ii) the origin and relative success of bodyplans; (iii) community ecology and evolution.

Early Paleozoic Hyolitha from North America: reexamination of Walcott's and Resser's type specimens

1988 ◽  
Vol 62 (2) ◽  
pp. 218-233 ◽  
Author(s):  
John Mark Malinky
Keyword(s):  
North America ◽  
Lower Cambrian ◽  
Type Species ◽  
New Genus ◽  
Early Paleozoic ◽  
Type Specimens ◽  
Middle Cambrian ◽  
Upper Cambrian ◽  
New Family ◽  
The Family

Concepts of the family Hyolithidae Nicholson fide Fisher and the genera Hyolithes Eichwald and Orthotheca Novak have been expanded through time to encompass a variety of morphologically dissimilar shells. The Hyolithidae is here considered to include only those hyolithid species which have a rounded (convex) dorsum; slopes on the dorsum are inflated, and the venter may be flat or slightly inflated. Hyolithes encompasses species which possess a low dorsum and a prominent longitudinal sulcus along each edge of the dorsum; the ligula is short and the apertural rim is flared. The emended concept of Orthotheca includes only those species of orthothecid hyoliths which have a subtriangular transverse outline and longitudinal lirae covering the shell on both dorsum and venter.Eighteen species of Hyolithes and one species of Orthotheca from the Appalachian region and Western Interior were reexamined in light of more modern taxonomic concepts and standards of quality for type material. Reexamination of type specimens of H. similis Walcott from the Lower Cambrian of Newfoundland, H. whitei Resser from the Lower Cambrian of Nevada, H. billingsi Walcott from the Lower Cambrian of Nevada, H. gallatinensis Resser from the Upper Cambrian of Wyoming, and H. partitus Resser from the Middle Cambrian of Alabama indicates that none of these species represents Hyolithes. Hyolithes similis is here included under the new genus Similotheca, in the new family Similothecidae. Hyolithes whitei is designated as the type species of the new genus Nevadotheca, to which H. billingsi may also belong. Hyolithes gallatinensis is referred to Burithes Missarzhevsky with question, and H. partitus may represent Joachimilites Marek. The type or types of H. attenuatus Walcott, H. cecrops Walcott, H. comptus Howell, H. cowanensis Resser, H. curticei Resser, H. idahoensis Resser, H. prolixus Resser, H. resseri Howell, H. shaleri Walcott, H. terranovicus Walcott, and H. wanneri Resser and Howell lack shells and/or other taxonomically important features such as a complete aperture, rendering the diagnoses of these species incomplete. Their names should only be used for the type specimens until better preserved topotypes become available for study. Morphology of the types of H.? corrugatus Walcott and “Orthotheca” sola Resser does not support placement in the Hyolitha; the affinities of these species are uncertain.

Identification and significance of late Holocene tephra from Otter Creek, southern British Columbia, and localities in west-central Alberta

1977 ◽  
Vol 14 (11) ◽  
pp. 2593-2600 ◽  
Author(s):  
J. A. Westgate
Keyword(s):  
British Columbia ◽  
Late Holocene ◽  
Far North ◽  
West Central ◽  
Tephra Beds ◽  
Middle Unit ◽  
Mount St Helens

Three thin, light-coloured, ash-grade tephra beds occur within the uppermost metre of peat at Otter Creek bog in southern British Columbia. The youngest tephra is related to the ~2600 year old Bridge River tephra but is probably the product of a younger and weaker eruption that directed tephra to the southeast of the vent, believed to be located in the Meager Mountain district of southwestern British Columbia. The middle unit is ~2100 years old and is tentatively correlated with one of the upper beds of set P tephra of Mount St. Helens in Washington. The lowermost tephra is equivalent to the Yn bed of set Y, derived from an eruption of Mount St. Helens about 3400 years ago.The Yn tephra has been located as far north as Entwistle in west-central Alberta but mineralogically and chemically similar tephra elsewhere in this region is ~4300 years old and thus represents an older part of the Y set. Significant compositional differences between these two extensive members of the Y set have not yet been recognized.

Articulated halkieriids from the Lower Cambrian of North Greenland and their role in early protostome evolution

1995 ◽  
Vol 347 (1321) ◽  
pp. 305-358 ◽  
Keyword(s):  
Body Size ◽  
Molecular Biology ◽  
Lower Cambrian ◽  
Burgess Shale ◽  
Internal Anatomy ◽  
Middle Cambrian ◽  
Functional Consequence ◽  
Primitive State ◽  
North Greenland

Articulated halkieriids of Halkieria evangelista sp. nov. are described from the Sirius Passet fauna in the Lower Cambrian Buen Formation of Peary Land, North Greenland. Three zones of sclerites are recognizable: obliquely inclined rows of dorsal palmates, quincuncially inserted lateral cultrates and imbricated bundles of ventro-lateral siculates. In addition there is a prominent shell at both ends, each with radial ornamentation. Both sclerites and shells were probably calcareous, but increase in body size led to insertion of additional sclerites but marginal accretion of the shells. The ventral sole was soft and, in life, presumably muscular. Recognizable features of internal anatomy include a gut trace and possible musculature, inferred from imprints on the interior of the anterior shell. Halkieriids are closely related to the Middle Cambrian Wixaxia , best known from the Burgess Shale: this clade appears to have played an important role in early protostome evolution. From an animal fairly closely related to Wixaxia arose the polychaete annelids; the bundles of siculate sclerites prefigure the neurochaetae whereas the dorsal notochaetae derive from the palmates. Wixaxia appears to have a relic shell and a similar structure in the sternaspid polychaetes may be an evolutionary remnant. The primitive state in extant polychaetes is best expressed in groups such as chrysopetalids, aphroditaceans and amphinomids. The homology between polychaete chaetae and the mantle setae of brachiopods is one line of evidence to suggest that the latter phylum arose from a juvenile halkieriid in which the posterior shell was first in juxtaposition to the anterior and rotated beneath it to provide the bivalved condition of an ancestral brachiopod. H. evangelista sp. nov. has shells which resemble those of a brachiopod; in particular the posterior one. From predecessors of the halkieriids known as siphogonuchitids it is possible that both chitons (polyplacophorans) and conchiferan molluscs arose. The hypothesis of halkieriids and their relatives having a key role in annelid—brachiopod—mollusc evolution is in accord with some earlier proposals and recent evidence from molecular biology. It casts doubt, however, on a number of favoured concepts including the primitive annelid being oligochaetoid and a burrower, the brachiopods being deuterostomes and the coelom being an archaic feature of metazoans. Rather, the annelid coelom arose as a functional consequence of the transition from a creeping halkieriid to a polychaete with stepping parapodial locomotion.

The “evolution” of Anomalocaris and its classification in the arthropod class Dinocarida (nov.) and order Radiodonta (nov.)

1996 ◽  
Vol 70 (2) ◽  
pp. 280-293 ◽  
Author(s):  
Desmond Collins
Keyword(s):  
British Columbia ◽  
Sea Cucumber ◽  
Great Difficulty ◽  
Burgess Shale ◽  
Middle Cambrian ◽  
The Past ◽  
History Of ◽  
The Many ◽  
Life On Earth ◽  
Mistaken Identification

The remarkable “evolution” of the reconstructions of Anomalocaris, the extraordinary predator from the 515 million year old Middle Cambrian Burgess Shale of British Columbia, reflects the dramatic changes in our interpretation of early animal life on Earth over the past 100 years. Beginning in 1892 with a claw identified as the abdomen and tail of a phyllocarid crustacean, parts of Anomalocaris have been described variously as a jellyfish, a sea-cucumber, a polychaete worm, a composite of a jellyfish and sponge, or have been attached to other arthropods as appendages. Charles D. Walcott collected complete specimens of Anomalocaris nathorsti between 1911 and 1917, and a Geological Survey of Canada party collected an almost complete specimen of Anomalocaris canadensis in 1966 or 1967, but neither species was adequately described until 1985. At that time they were interpreted by Whittington and Briggs to be representatives of “a hitherto unknown phylum.”Here, using recently collected specimens, the two species are newly reconstructed and described in the genera Anomalocaris and Laggania, and interpreted to be members of an extinct arthropod class, Dinocarida, and order Radiodonta, new to science. The long history of inaccurate reconstruction and mistaken identification of Anomalocaris and Laggania exemplifies our great difficulty in visualizing and classifying, from fossil remains, the many Cambrian animals with no apparent living descendants.

The initiation of the early Paleozoic Cordilleran miogeocline: evidence from the uppermost Proterozoic – Lower Cambrian Hamill Group of southeastern British Columbia

1988 ◽  
Vol 25 (1) ◽  
pp. 1-19 ◽  
Author(s):  
William J. Devlin ◽  
Gerard C. Bond
Keyword(s):  
British Columbia ◽  
Lower Cambrian ◽  
Direct Evidence ◽  
Thermal Anomaly ◽  
Passive Margin ◽  
Early Paleozoic ◽  
Upper Proterozoic ◽  
Windermere Supergroup ◽  
Depositional Setting ◽  
Thermal Subsidence

The uppermost Proterozoic–Lower Cambrian Hamill Group of southeastern British Columbia contains geologic evidence for a phase of extensional tectonism that led directly to the onset of thermally controlled subsidence in the Cordilleran miogeocline. Moreover, the Hamill Group contains the sedimentological record of the passage of the ancient passive margin from unstable tectonic conditions associated with rifting and (or) the earliest phases of thermal subsidence to post-rift conditions characterized by stabilization of the margin and dissipation of the thermal anomaly generated during the rift phase (the rift to post-rift transition). Widespread uplift that occurred prior to and during the deposition of the lower Hamill Group is indicated by an unconformable relation with the underlying Windermere Supergroup and by stratigraphic relations between Middle and Upper Proterozoic strata and unconformably overlying upper Lower Cambrian quartz arenites (upper Hamill Group) in the southern borderlands of the Hamill basin. In addition, the coarse grain size, the feldspar content, the depositional setting, and the inferred provenance of the lower Hamill Group are all indicative of the activation of basement sources along the margins of the Hamill basin. Geologic relations within the Hamill Group that provide direct evidence for extensional tectonism include the occurrence of thick sequences of mafic metavolcanics and rapid vertical facies changes that are suggestive of syndepositional tectonism.Evidence of extensional tectonism in the Hamill Group directly supports inferences derived from tectonic subsidence analyses that indicate the rift phase that immediately preceded early Paleozoic post-rift cooling could not have occurred more than 10–20 Ma prior to 575 ± 25 Ma. These data, together with recently reported isotopic data that suggest deposition of the Windermere Supergroup began ~730–770 Ma, indicate that the rift-like deposits of the Windermere Supergroup are too old to represent the rifting that led directly to the deposition of the Cambro-Ordovician post-rift strata. Instead, Windermere sedimentation was apparently initiated by an earlier rift event, probably of regional extent, that was part of a protracted, episodic rift history that culminated with continental breakup in the latest Proterozoic – Early Cambrian.

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