scholarly journals Fossils of the Burgess Shale, a national treasure in Yoho National Park, British Columbia

1985 ◽  
Author(s):  
S C Morris ◽  
H B Whittington
2015 ◽  
Vol 89 (1) ◽  
pp. 82-95 ◽  
Author(s):  
Steven T. LoDuca ◽  
Jean-Bernard Caron ◽  
James D. Schiffbauer ◽  
Shuhai Xiao ◽  
Anthony Kramer

AbstractTo investigate the phylogenetic affinity of Yuknessia simplex Walcott, 1919, scanning electron microscopy was applied to the Burgess Shale (Cambrian Series 3, Stage 5) type material and to new material from the Trilobite Beds (Yoho National Park) and specimens from the Cambrian of Utah. On the basis of fine-scale details observed using this approach, including banding structure interpreted as fusellae, Yuknessia Walcott, 1919 is transferred from the algae, where it resided for nearly a century, to the extant taxon Pterobranchia (Phylum Hemichordata). Considered as such, Yuknessia specimens from the Trilobite Beds and Spence Formation (Utah) are amongst the oldest known colonial pterobranchs. Two morphs regarded herein as two different species are recognized from the Trilobite Beds based on tubarium morphology. Yuknessia simplex has slender erect tubes whereas Yuknessia stephenensis n. sp., which is also known in Utah, has more robust erect tubes. The two paratypes of Y. simplex designated by Walcott (1919) are formally removed from Yuknessia and are reinterpreted respectively as an indeterminate alga and Dalyia racemata Walcott, 1919, a putative red alga.


Paleobiology ◽  
2020 ◽  
Vol 46 (1) ◽  
pp. 58-81 ◽  
Author(s):  
Karma Nanglu ◽  
Jean-Bernard Caron ◽  
Robert R. Gaines

AbstractThe middle (Wuliuan Stage) Cambrian Burgess Shale is famous for its exceptional preservation of diverse and abundant soft-bodied animals through the “thick” Stephen Formation. However, with the exception of the Walcott Quarry (Fossil Ridge) and the stratigraphically older Tulip Beds (Mount Stephen), which are both in Yoho National Park (British Columbia), quantitative assessments of the Burgess Shale have remained limited. Here we first provide a detailed quantitative overview of the diversity and structure of the Marble Canyon Burgess Shale locality based on 16,438 specimens. Located 40 km southeast of the Walcott Quarry in Kootenay National Park (British Columbia), Marble Canyon represents the youngest site of the “thick” Stephen Formation. We then combine paleoecological data sets from Marble Canyon, Walcott Quarry, Tulip Beds, and Raymond Quarry, which lies approximately 20 m directly above the Walcott Quarry, to yield a combined species abundance data set of 77,179 specimens encompassing 234 species-level taxa. Marble Canyon shows significant temporal changes in both taxonomic and ecological groups, suggesting periods of stasis followed by rapid turnover patterns at local and short temporal scales. At wider geographic and temporal scales, the different Burgess Shale sites occupy distinct areas in multivariate space. Overall, this suggests that the Burgess Shale paleocommunity is far patchier than previously thought and varies at both local and regional scales through the “thick” Stephen Formation. This underscores that our understanding of Cambrian diversity and ecological networks, particularly in early animal ecosystems, remains limited and highly dependent on new discoveries.


Paleobiology ◽  
2015 ◽  
Vol 42 (1) ◽  
pp. 27-53 ◽  
Author(s):  
Lorna J. O’Brien ◽  
Jean-Bernard Caron

AbstractThe Tulip Beds locality on Mount Stephen (Yoho National Park, British Columbia) yields one of the most abundant and diverse (~10,000 specimens in 110 taxa) Burgess Shale fossil assemblages in the Canadian Rockies. Detailed semi quantitative and quantitative analyses of this assemblage suggest strong similarities with the Walcott Quarry on Fossil Ridge. Both assemblages are dominated by epibenthic, sessile, and suspension feeding taxa, mostly represented by arthropods and sponges and have comparable diversity patterns, despite sharing only about half the genera. However, the Tulip Beds has a higher relative abundance of suspension feeders and taxa of unknown affinity compared to the Walcott Quarry. These biotic variations are probably largely attributable to ecological and evolutionary differences between the two temporally distinct communities that adapted to similar, but not identical, environmental settings. For instance, the Tulip Beds is farther away from the Cathedral Escarpment than the Walcott Quarry. The Tulip Beds and Walcott Quarry assemblages are more similar to each other than either one is to the assemblages of the Chengjiang biota, although the relative diversity of major taxonomic groups and ecological patterns are similar in all assemblages. The conserved diversity patterns and ecological structures among sites suggest that the ecological composition of Cambrian Burgess Shale-type communities was relatively stable across wide geographic and temporal scales.


2015 ◽  
Author(s):  
Iain J Reid

Since the 1900s, dinosaur fossils have been discovered from Jurassic to Cretaceous age strata, from all across the prairie provinces of Canada and the Western United States, yet little material is known from the outer provinces and territories. In British Columbia, fossils have long been uncovered from the prevalent mid-Cambrian Burgess Shale, but few deposits date from the Mesozoic, and few of these are dinosaurian. The purpose of this paper is to review the history of dinosaurian body fossils in British Columbia. The following dinosaurian groups are represented: coelurosaurians, thescelosaurids, iguanodontians, ankylosaurs and hadrosaurs.


1996 ◽  
Vol 70 (2) ◽  
pp. 280-293 ◽  
Author(s):  
Desmond Collins

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.


Zootaxa ◽  
2019 ◽  
Vol 4666 (1) ◽  
pp. 1-180 ◽  
Author(s):  
VALERIE M. BEHAN-PELLETIER ◽  
ZOË LINDO

This checklist of the oribatid fauna of Canada and Alaska (excluding Astigmata) includes 580 identified species in 249 genera and 96 families. The known fauna of Canada includes 556 identified species in 247 genera, and that of Alaska includes 182 species in 95 genera; 39 of the 42 oribatid superfamilies are represented. We further list ~ 300 species that are currently unidentified, and possibly undescribed. In addition, we list 42 genera that are represented only by unidentified and probably undescribed species. For each species we give combinations and synonymies, specific locations in Alaska and the Provinces and Territories of Canada, habitats, and biogeography.                There are 182 identified species known for Alaska, 152 for Yukon, 122 for Northwest Territories, 58 for Nunavut; 210 for British Columbia, 213 for Alberta, 15 for Saskatchewan, 84 for Manitoba, 167 for Ontario, 210 for Québec, 110 for Nova Scotia, 77 for New Brunswick, 84 for Newfoundland and 6 for Prince Edward Island. The known fauna of Canada is smaller than that of Austria, and is approximately equivalent to that of the Czech Republic. As these countries are much smaller in size than Canada and less ecologically diverse, we consider the Canadian and Alaskan fauna are at most 25% known. The paucity of these data reflects the absence of taxonomic and faunistic studies on Oribatida in State, Provinces or Territories, and especially in the Canadian and Alaskan National Park systems and the hundreds of Provincial Parks.                Despite the almost 90% increase in described species since the catalogue of Marshall et al. (1987), there is a need for focussed, coordinated research on Oribatida in the natural regions throughout Canada and Alaska, and for monographs on families and genera with large numbers of undescribed species, such as Brachychthoniidae, Damaeidae, Cepheidae, Liacaridae, Oppiidae, Suctobelbidae, Hydrozetidae, Phenopelopidae, Scheloribatidae, Haplozetidae and Galumnidae. 


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