Characteristic trace fossils in nearshore to offshore sequences, Upper Cretaceous of east-central Utah

1984 ◽  
Vol 21 (2) ◽  
pp. 200-219 ◽  
Author(s):  
James D. Howard ◽  
Robert W. Frey

More than 20 trace fossil species occur in marine facies of the Cretaceous Star Point and Blackhawk formations in the Book Cliffs and Wasatch Plateau provinces of Utah. Major genera include Ancorichnus, Arenicolites, Aulichnites, Chondrites, Conichnus, Cylindrichnus, Medousichnus, Ophiomorpha, Palaeophycus, Planolites, Rosselia, Schaubcylindrichnus, Scolicia, Skolithos, Teichichnus, Teredolites, and Thalassinoides. Newly named taxa include Ancorichnus capronus, Medousichnus loculatus, and Rosselia chonoides.Most trace fossils occur in characteristic, albeit intergradational ichnofacies correlative with major lithofacies of regressive nearshore to offshore sequences. The latter include foreshore, foreshore–shoreface transition, shoreface, and offshore facies. Landward facies are typified by clean, well sorted, well stratified, sparsely burrowed sandstones. Seaward facies, except where interrupted by hummocky bedded sandstones, exhibit successively less pure, less well sorted and stratified, more intensely bioturbated, finer grained sandstones, siltstones, and mudstones.Characteristic ichnofacies and lithofacies in the Cretaceous of east-central Utah should provide potentially useful models for reconstruction of nearshore to offshore sequences elsewhere, especially in the Western Interior Region of North America.

1998 ◽  
Vol 72 (4) ◽  
pp. 773-778 ◽  
Author(s):  
Richard G. Bromley ◽  
A. A. Ekdale

The trace fossilOphiomorpha irregulaireFrey, Howard and Pryor, 1978, has been described chiefly from the Campanian (Upper Cretaceous) of the Book Cliffs of Carbon County, central Utah, U.S.A. Owing to the lack of type specimens and a well-defined type locality, a neotype and new paratypes are designated. Abundant material in the Spring Canyon Member of the Blackhawk Formation at Coal Creek Canyon, Book Cliffs, serves to supply a type locality and allows a more detailed description of the trace fossil than has been available hitherto, leading to an emended diagnosis. At the type locality,O. irregulaireis a shallow-tier trace fossil occurring in marine, delta-front or back-barrier, muddy, fine-grained sandstone. It probably represents the work of a crustacean deposit feeder.


1994 ◽  
Vol 31 (5) ◽  
pp. 767-782 ◽  
Author(s):  
H. J. Hofmann ◽  
M. P. Cecile ◽  
L. S. Lane

Trace fossil assemblages from green and maroon argillites at 34 localities in the British Mountains and Barn Mountains of northernmost Yukon, and 3 localities in the Grant Land Formation of northern Ellesmere Island contain abundant Planolites spp., Oldhamia curvata, Oldhamia flabellata, and Oldhamia radiata, and rare Oldhamia antiqua, Oldhamia? wattsi (n.comb.), Bergaueria hemispherica, Cochlichnus sp., Didymaulichnus? sp., Helminthoidichnites sp., Monomorphichnus sp., Protopaleodictyon sp., and Tuberculichnus? sp. Additionally, 11 new sites in the Selwyn Mountains of north-central Yukon have yielded an ichnofauna including Helminthorhaphe sp., O. curvata, O. flabellata, O. radiata, Plagiogmus? sp., Planolites spp., and unidentified small hemispherical traces. All these assemblages are interpreted as Early Cambrian to early Middle Cambrian, based on comparison with Oldhamia-bearing ichnofaunas of similar age in North America, Argentina, and western Europe, and on archaeocyathids and olenellids in overlying units.


I wish to emphasize the im portance of trace fossil evidence in studying the terrestrialization of invertebrates. Associations of trace fossils of arthropod origin are known from the late Silurian and Devonian non-marine sediments in the Welsh Borders, Scotland (Midland Valley and Orcadian basins), Norway (Ringerike and Hornelen basins), Spitzbergen, Appalachians of North America and Antarctica (Pollard et al . 1982, figure 15; Pollard & W alker 1984, figure 3).


Phytotaxa ◽  
2017 ◽  
Vol 297 (1) ◽  
pp. 62 ◽  
Author(s):  
ALEXANDER B. DOWELD

The nomenclature of some fossil and extant homonymic species of Aralia is resolved. Aralia laevis J. Wen (extant) is replaced by a new name A. indonesica nom. nov., because of earlier homonym, A. laevis E.M.Reid (fossil). Aralia debilis J. Wen is rehabilitated as a legitimate substitute to the later homonym, A. elegans Ho, due to the existence of several earlier homonyms, the extant A. elegans Linden ex Koch, A. elegans Cunn. ex W.Hill and A. elegans Hort. ex Saporta, and the fossil A. elegans Velenovský. Additional four new replacement names are proposed for fossil species based on endocarp remains from the Miocene sediments of Siberia: Aralia asiatica nom. nov. for A. rugosa Dorofeev non Blume, A. mammuthica nom. nov. for A. dubia V.P. Nikitin non Sprengel nec Fontaine, A. borealis nom. nov. for A. tertiaria Dorofeev non Pilar, and A. tobolica nom. nov. for A. lucida Dorofeev non Hasskarl. The later homonym A. angustiloba Kolakovsky non Lesquereux, based on the fossil foliage from the Pliocene sediments of Transcaucasus, is transferred into Brassaiopsis as B. kolakovskyana nom. nov. Fossil species A. furcata, described on the basis of leaf remains from the Upper Cretaceous (Cenomanian) of Bohemia, is transferred into Haliserites as H. furcatus comb. nov. The fossil later homonym A. serrata Knowlton non Saporta, described on the basis of leaf remains from the Palaeocene of North America, is transferred into Platanus as P. serrata nom. nov.


2015 ◽  
Vol 52 (8) ◽  
pp. 537-541 ◽  
Author(s):  
Dennis R. Braman

The fossil pollen genus Morinoipollenites has been frequently reported in strata from the Upper Cretaceous of northern China and southeastern Russia. Pollen grains belonging to a single fossil species, Morinoipollenites normalis, have been only rarely encountered in Upper Cretaceous strata of North America. Just five specimens of Morinoipollenites have been recovered from sites of definite or probable Maastrichtian age in Alaska, Alberta, Saskatchewan, and Colorado. It is argued that the rarity in North America, common Asian occurrences, large size of pollen grains, and complex morphology of the pollen favour these pollen grains having been transported to North America from Asia by some vector. The transporting vector would most likely have been a flying organism based on the life styles of the producing plants and transporting organisms, long distance of transport, and morphology of the pollen grains.


1995 ◽  
Vol 32 (5) ◽  
pp. 631-643 ◽  
Author(s):  
James D. Gardner ◽  
Anthony P. Russell ◽  
Donald B. Brinkman

Four valid species of trionychine trionychid turtles are recognized from the Upper Cretaceous (mid-Campanian; Judithian) Judith River Group, western North America. Cladistic analysis of extant and Judith River Group trionychines supports referral of three fossil species to Aspideretoides gen. nov. and one fossil species to Apalone, the genus of extant North American trionychines. The taxonomic diversity of Judith River Group trionychids is less than that of younger Maastrichtian and Paleocene assemblages from the Western Interior, largely because of the absence of plastomenine trionychids in the Judith River Group assemblage.


1999 ◽  
Vol 73 (5) ◽  
pp. 872-885 ◽  
Author(s):  
Daniel L. Geiger ◽  
Lindsey T. Groves

Compared to their Recent counterparts, fossil abalone are rare and poorly known. Their taxonomy is problematic, because most of the 35 fossil species have been described from single specimens and shell characteristics of Recent species are extremely plastic. Thus, the use of fossil species in phylogeny is questionable. Abalone first appear in the Upper Cretaceous (Maastrichian) with one species each in California and the Caribbean, are unknown in the Paleocene, and appear again in the late Eocene and Oligocene of New Zealand and Europe. They are regularly found from the late Miocene to the Recent in tropical to temperate regions worldwide. Most records are from intensely studied areas: SW North America, Caribbean, Europe, South Africa, Japan, and Australia. Despite their highest present-day diversity being found in the Indo-Pacific, their scarcity in the fossil record in this region is remarkable. The family may have originated in the central Indo-Pacific, Pacific Rim, or Tethys. An extensive list of all known fossil records including new ones from Europe and western North America is given. Fossil and Recent abalone both apparently lived in the shallow, rocky sublittoral in tropical and temperate climates. No on-shore/off-shore pattern is detected.


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