scholarly journals Fractured clasts in the Mt Currie Conglomerate at Kata Tjuta (Central Australia): evidence of Early Cambrian earthquakes?

2020 ◽  
Vol 46 (1) ◽  
pp. 29 ◽  
Author(s):  
Antek K. Tokarski ◽  
Piotr J. Strzelecki

Lower Cambrian Mt Currie conglomerate at Kata Tjuta bornhardts (Central Australia) bears numerous fractured clasts. Clast-cutting fractures are restricted to particular clasts, the matrix of the conglomerate is not fractured. The fractures are tectonic joints of two sets. The joints were formed due to either seismic or aseismic deformation. In the former case, the fractures may result from Early Paleozoic earthquakes.

2008 ◽  
Vol 82 (5) ◽  
pp. 884-905 ◽  
Author(s):  
Ed Landing ◽  
Susan C. Johnson ◽  
Gerd Geyer

The Cambrian inlier at Beaver Harbour, southern New Brunswick, is now confidently referred to the marginal platform of the late Proterozoic–Early Paleozoic Avalon microcontinent. The sub-trilobitic Lower Cambrian Chapel Island and Random Formations are unconformably overlain by the mafic volcanic-dominated Wade's Lane Formation (new). Late Early Cambrian trilobites and small shelly taxa in the lowest Wade's Lane demonstrate a long Random–Wade's Lane hiatus (middle Terreneuvian–early Branchian). Latest Early–middle Middle Cambrian pyroclastic volcanism produced a volcanic edifice at Beaver Harbour that is one of three known volcanic centers that extended 550 km along the northwest margin of Avalon. Middle Middle Cambrian sea-level rise, probably in theParadoxides eteminicusChron, mantled the extinct volcanics with gray-green mudstone and limestone of the Fossil Brook Member. Black, dysoxic mudstone of the upper Manuels River Formation (upper Middle Cambrian,P. davidisZone) is the youngest Cambrian unit in the Beaver Harbour inlier.Lapworthella cornu(Wiman, 1903) emend., a senior synonym of the genotypeL. nigra(Cobbold, 1921),Hyolithellus sinuosusCobbold, 1921, and probablyAcrothyra seraMatthew, 1902a, range through the ca. 8 m.y. of the trilobite-bearing upper Lower Cambrian, andH. sinuosusandA. serapersist into the middle Middle Cambrian.Lapworthella cornuandH. sinuosusreplaced the tropical taxaL. schodackensis(Lochman, 1956) andH. micansBillings, 1872, in cool-water Avalon.


1988 ◽  
Vol 62 (2) ◽  
pp. 218-233 ◽  
Author(s):  
John Mark Malinky

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.


2004 ◽  
Vol 41 (11) ◽  
pp. 1273-1283 ◽  
Author(s):  
Christian B Skovsted ◽  
John S Peel ◽  
Christian J Atkins

The cap-shaped Early Cambrian fossil Triplicatella, previously known only from Australia, is reported from the upper Lower Cambrian of North and North-East Greenland, western Newfoundland, and Siberia. The occurrence of Triplicatella in Laurentia strengthens faunal ties between Laurentia and the Australian margin of Gondwana in late Early Cambrian times and supports hypotheses advocating the close proximity for the two palaeocontinents. Two new species, Triplicatella sinuosa n. sp., and T. peltata n. sp. are described, morphological details of which help elucidate the functional morphology and taxonomic affinity of the group. Three opercular types attributable to Triplicatella are left in open taxonomy. The postulated affinity of Triplicatella to hyoliths is confirmed, although the genus can not be placed within either of the two orders of hyoliths currently recognized.


1988 ◽  
Vol 25 (1) ◽  
pp. 1-19 ◽  
Author(s):  
William J. Devlin ◽  
Gerard C. Bond

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.


2000 ◽  
Vol 74 (5) ◽  
pp. 858-878 ◽  
Author(s):  
Stephen R. Westrop ◽  
Ed Landing

The Hanford Brook Formation, one of the classic Cambrian units of Avalonian North America, contains at least eight species of endemic trilobites, including Berabichia milleri Westrop n. sp., that are assigned to seven genera. The vertical succession of faunas is far more complex than has been recognized previously, with each member containing a lithofacies-specific assemblage. These are, in ascending order: a bradoriid-linguloid Association without trilobites in the nearshore St. Martin's Member, a Protolenus Association in dysaerobic siltstones and sandstones of the Somerset Street Member, and a Kingaspidoides-Berabichia Association in hummocky cross-stratified sandstones of the Long Island Member that overlie a parasequence boundary at Hanford Brook. Due to the breakdown of biogeographic barriers in the late Early Cambrian, two new species-based zones, the Protolenus elegans and Kingaspidoides cf. obliquoculatus zones, share trilobite genera with the Tissafinian Stage of Morocco. This generic similarity has been the basis for correlation of this upper Lower Cambrian interval on the Avalon continent with the West Gondwanan lowest Middle Cambrian. However, the clear facies control on the occurrence of genera in the Hanford Brook Formation and the presence of an abrupt faunal break and unconformity at the base of the Tissafinian in Morocco makes this correlation questionable. The Hanford Brook Formation may represent a late Early Cambrian interval unknown in Gondwana. Sequence-stratigraphic criteria even raise the possibility that the Protolenus Association is the biofacies equivalent of Callavia broeggeri Zone faunas of the Brigus Formation of Newfoundland, Nova Scotia and Massachusetts.


1992 ◽  
Vol 6 ◽  
pp. 272-272 ◽  
Author(s):  
Philip W. Signor

A handful of mass extinctions, scattered through the Phanerozoic, forever changed the course of life on Earth, eliminating large numbers of clades from the evolutionary race and allowing the survivors to diversify following the extinction. These ecological-evolutionary upheavals extirpated whole communities and eliminated otherwise successful clades from the evolutionary race. While the mechanism(s) responsible for most mass extinctions remain to be identified, their impact on the biosphere is self-evident. Thus, recognition of a previously overlooked, severe extinction early in the Phanerozoic provides important new insights and perspectives on the history of lifeIn the course of research on the biogeographic distribution of Early Cambrian metazoan taxa, I compiled a database on the geographic and stratigraphic distribution of metazoan genera. The data are derived from the primary literature on the paleogeographic and stratigraphic distributions and systematics of Early Cambrian fossils. The Russian zonation scheme for the Siberian Platform (incorporating four stages, in ascending order: Tommotian, Atabanian, Botomian, and Toyonian) was employed for biostratigraphic correlations. Correlations of other regions to the Siberian stages were based upon work by F. Debrenne and her colleagues on archaeocyathans and upon M. D. Brasier's correlations from small shelly fossils. While there is no accepted global correlation scheme for Lower Cambrian strata, this approach yields results that are useful at the four-stage level of resolution. The data base currently includes more than 850 genera.Examination of the aggregate data reveals a substantial reduction (>60%) in the global total of genera extant in the Toyonian, in comparison to the Botomian stage. The extinction rate of genera at the end of the Botomian exceeds 80 percent. By comparison, the end-Permian extinction eliminated slightly more than 60 percent of the extant genera.In addition to the general reduction in generic diversity, Brasier (1982) has documented a fall in sea level and reduction in the shelf area. Associated with this regression was a loss of reef-forming archaeocyathan genera. While a small number of archaeocyathan genera persisted into the Toyonian (and a few genera have been reported from Late Cambrian strata in Antarctica), the bulk of archaeocyath diversity was lost in the Botomian. The losses in diversity, extermination of reef-forming organisms, and high turnover in conjunction with a marine regression matches the pattern observed at most other mass extinctions.It is remarkable that this relatively severe extinction has gone mostly unnoticed by paleobiologists. Much of the data is relatively new, a product of intense international study of early metazoan faunas. Most likely, the mass of data produced by Lower Cambrian specialists over the past ten years has yet to reach the treatises and monographs where it can be easily summarized. Also, resolution of patterns within the Early Cambrian has waited on the development of correlations and a satisfactory zonation. Indeed, detailed study of the Botomian extinction will await more accurate correlations.


1995 ◽  
Vol 132 (5) ◽  
pp. 473-483 ◽  
Author(s):  
P. W. G. Tanner

AbstractThe Lower Cambrian Leny Limestone at Callander in Scotland lies within a sequence of palecoloured grits and dark slates (here named the Keltie Water Grit Formation (KWGF)) which has lithological similarities with members of the Highland Border Complex (HBC) (Ordovician) seen elsewhere along the Highland Border. The Keltie Water Grit Formation has a transitional boundary with a grit-slate sequence of undoubted Dalradian parentage; as the ‘Leny Grits’ of previous workers include both the KWGF and part of the Dalradian sequence, this term is now rendered invalid. The entire sequence youngs upwards from the Dalradian to the top of the overlying Keltie Water Grit Formation, shares the same structural sequence and geometry, and has the same facing and vergence direction on the main cleavage. All field and petrographic data are consistent with a minimum age of post-early Cambrian for the Grampian event, the main orogenic event to affect the Dalradian. Examination of critical sections elsewhere across the Highland Border shows that there is an apparently consistent stratigraphical and structural relationship between the Highland Border Complex and the Dalradian which, as suggested by some previous workers, would require the Grampian event to be post-Arenig in age. However, we are faced with a so-far unresolved paradox that there are certain palaeontological and radiometric data which are in conflict with this conclusion, and support the alternative hypothesis that the Highland Border Complex docked with the Dalradian in post-Ordovician times.


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