Dinosaur Park Formation
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The Dinosaur Park Formation is the uppermost member of the Belly River Group (also known as the Judith River Group), a major geologic unit in southern Alberta. It was deposited during the Campanian stage of the Late Cretaceous, between about 76.5 and 74.4 million years ago.[1] It was deposited in alluvial and coastal plain environments, and it is bounded by the nonmarine Oldman Formation below it and the marine Bearpaw Formation above it.[2]
The Dinosaur Park Formation contains dense concentrations of dinosaur skeletons, both articulated and disarticulated, which are often found with preserved remains of soft tissues. Remains of other animals such as fish, turtles, and crocodilians, as well as plant remains, are also abundant.[3] The formation has been named after Dinosaur Provincial Park, a UNESCO World Heritage Site where the formation is well exposed in the badlands that flank the Red Deer River.[4]
Research history
The Dinosaur Park Formation has been a significant source of terrestrial vertebrate fossils for over a century. The first recorded account of fossils was in 1871 by the priest Jean-Baptiste L’Heureux who was shown bones of the "grandfather of the buffalo" by the Blackfoot Confederacy he was living with, though these notes were never published. Official reports of dinosaur bones in western Canada were reported by George Mercer Dawson in 1874 from southern Saskatchewan and Alberta along the Milk River. Further discoveries by Dawson and his colleagues of the Geological Survey of Canada continued in the 1880s, including the 1884 discovery by Joseph Burr Tyrrell of the skull of a theropod identified as Laelaps by American palaeontologist Edward Drinker Cope but named in 1905 as Albertosaurus by American palaeontologist Henry Fairfield Osborn. In 1889 rich fossil beds in the areas of Deadlodge CanyonTemplate:Efn and Berry CreekTemplate:Efn were found by Thomas Chesmer Weston along the Red Deer River. The areas along the Red Deer River would be more completely surveyed by Canadian palaeontologist Lawrence Lambe from 1897 until 1901, when he, along with Osborn, described the fossils found in what was then considered to be the Belly River Formation of mid-Cretaceous age.[5]
Geological setting
The Dinosaur Park Formation is composed of sediments that were derived from the erosion of the mountains to the west. It was deposited on an alluvial to coastal plain by river systems that flowed eastward and southeastward to the Bearpaw Sea, a large inland sea that was part of the Western Interior Seaway. That sea gradually inundated the adjacent coastal plain, depositing the marine shales of the Bearpaw Formation on top of the Dinosaur Park Formation.[2]
The Dinosaur Park Formation is about Script error: No such module "convert". thick at Dinosaur Park. The lower portion of the formation was laid down in fluvial channel environments and consists primarily of fine- to medium-grained, crossbedded sandstones. The upper portion, which was deposited in overbank and floodplain environments, consists primarily of massive to laminated, organic-rich mudstones with abundant root traces, and thin beds of bentonite. The Lethbridge Coal Zone, which consists of several seams of low-rank coal interbedded with mudstones and siltstones, marks the top of the formation.[2]
The sediments of the Dinosaur Park Formation are similar to those of the underlying Oldman Formation and they were originally included in that formation. The two formations are separated by a regional disconformity, however, and are distinguished by petrographic and sedimentologic differences. In addition, articulated skeletal remains and bonebeds are rare in the Oldman Formation but abundant in the Dinosaur Park Formation.[4][2]
Biostratigraphy
The Dinosaur Park Formation can be divided into at least two distinct faunas. The lower part of the formation is characterized by the abundance of Corythosaurus and Centrosaurus. This group of species is replaced higher in the formation by a different ornithischian fauna characterized by the presence of Lambeosaurus and Styracosaurus.[6] The appearance of several new, rare species of ornithischian at the very top of the formation may indicate that a third distinct fauna had replaced the second during the transition into younger, non-Dinosaur Park sediments, at the same time an inland sea transgresses onto land, but there are fewer remains here. An unnamed pachyrhinosaur, Vagaceratops irvinensis, and Lambeosaurus magnicristatus may be more common in this third fauna.[7][8]
Template:Dinosaur Park Formation biostratigraphy
Fossil content
Amphibians
Remains of the following amphibians have been found in the formation:[9]
Albanerpetontidae (extinct, salamander-like amphibians)
- Habrosaurus prodilatus
- Lisserpeton
- Opisthotriton kayi
- Scapherpeton tectum
- unnamed caudatan
- Two indeterminate caudatans
- Two unnamed salientans
- Tyrrellbatrachus brinkmani[10]
- Hensonbatrachus kermiti[11]
Dinosaurs
Color key
|
Notes Uncertain or tentative taxa are in small text; |
Remains of the following dinosaurs have been found in the formation:[12][13]
Ornithischians
Remains of the following ornithischians have been found in the formation:[14]
Ankylosaurs
Numerous specimens that cannot be definitively assigned to ankylosaurs are known from the formation, including fragmentary cranial, dental, postcranial, and armour material.[15] As all ankylosaurids from the Campanian of Alberta and Montana were historically referred to Euoplocephalus sensu lato, the taxonomy is variable between studies and ranges from one to seven valid genera between the Dinosaur Park, Judith River, Two Medicine, and Horseshoe Canyon Formations.[16]
| Ankylosaurs from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location[17] | Stratigraphic position | Material | Notes | Images |
| Anodontosaurus[16] | A. inceptus | Hilda, Alberta[16] | Middle DPF | Two skulls, one with partial skeleton | Previously considered specimens of Euoplocephalus but then referred to Anodontosaurus lambei, otherwise only known from the Horseshoe Canyon Formation,[15] before being given the new species A. inceptus.[16] | File:Anodontosaurus lambei.tif |
| Dyoplosaurus[16][15] | D. acutosquameus | Q002 | Lower DPF | Partial skull and skeleton, two tail clubs | Thought to be a synonym of Euoplocephalus for a time but separated as a distinct taxon.[16][15] | File:Dyoplosaurus.tif |
| Edmontonia[18] | E. rugosidens | Q009, Q043, Q101, Q201, Q229, Q230 | Lower DPF | At least six partial skulls and skeletons | A nodosaurid also known from the Two Medicine Formation | File:Edmontonia half.jpg |
| Euoplocephalus[16][15] | E. tutus | Q059, Q198 | Lower to middle DPF | Partial skulls and skeletons | An ankylosaurid historically including all material from the formation. While some studies include up to 11 specimens even with Anodontosaurus, Dyoplosaurus and Scolosaurus separated, others limit it to 5 specimens and also separate Platypelta.[16][15] | File:Euoplocephalus TMP 1991.127.1.tif |
| Panoplosaurus[18] | P. mirus | Q008, Q228 | Middle DPF | Skulls and skeleton | A nodosaurid 1/3 less common than Edmontonia.[17] | File:Panoplosaurus.jpg |
| Platypelta[16] | P. coombsi | Q052 | Lowermost DPF | Skulls and skeletons | Considered specimens of Euoplocephalus by some studies,[15] but separated as a distinct genus by others.[16] | File:Platypelta AMNH 5337.tiff |
| Scolosaurus[16][15] | S. cutleri | Q080, Q089 | Base of DPF | Skull(s?) and skeletons | Thought to be a synonym of Euoplocephalus for a time but separated as a distinct taxon.[16] Has been suggested to include Oohkotokia from the Two Medicine Formation, and also to be from the top of the Oldman Formation if the quarry is incorrectly mapped.[15] | File:Scolosaurus mummy.jpg |
| S. thronus[16] | Quarry No. 112[16] | Upper DPF | Skull and partial skeletons | Considered indeterminate ankylosaurids or specimens of Euoplocephalus by some studies,[15] but separated as a distinct species by others.[16] | File:Euoplocephalus ROM1930.tif | |
Ceratopsians
An unnamed Pachyrhinosaurus-like taxon has been recovered from the formation.[19]
| Ceratopsians from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
| Centrosaurus | C. apertus | Middle, 76.2-75.5Ma ago[12] | "[Fifteen] skulls, several skeletons, all adult; abundant bone-bed material with rare juveniles and subadults."[20][21] C. nasicornis may be a synonym. | A centrosaurine ceratopsid | ||
| Chasmosaurus | C. belli | Middle, 76–75.5Ma ago[12] | "[Twelve] skulls, several skeletons."[20] | A chasmosaurine ceratopsid | ||
| C. russelli | Lower, 76.5-76Ma ago[12] | "[Six] complete or partial skulls."[22] | ||||
| Mercuriceratops | M. gemini[23] | Lower, ~77Ma ago[23] | "one apomorphic squamosal"[23] | A chasmosaurine ceratopsid | ||
| Monoclonius | M. lowei | A dubious centrosaurine ceratopsid. Possibly synonymous with Centrosaurus. | ||||
| Pentaceratops[24] | P. aquilonius[24] | Uppermost, 74.8 MA[24] | two frill fragments[24] | A dubious chasmosaurine ceratopsid that may be the same species as Spiclypeus shipporum.[25] | ||
| Spinops[26] | S. sternbergorum[26] | Lower, 76.5Ma[26] | "partial parietal bone, partial dentary, unidentifiable limb fragments, partial skull, and partial right squamosal."[26] | A centrosaurine ceratopsid.It may actually be from the upper Oldman Formation.[26] | ||
| Styracosaurus | S. albertensis | Upper, 75.5-75.2Ma ago[12] | "[Two] skulls, [three] skeletons, additional material in bone beds."[20] | A centrosaurine ceratopsid | ||
| Unescoceratops | U. koppelhusae | Partial lower jaw[27] | A leptoceratopsid thought to have been between one and two meters long and less than 91 kilograms. Its teeth were the roundest of all leptoceratopsids. | |||
| Vagaceratops | V. irvinensis | Upper, 75Ma ago[12] | "[Three] skulls, skeleton lacking tail."[22] | A chasmosaurine ceratopsid species previously classified as a species of Chasmosaurus.[28] | ||
Ornithopods
At least one indeterminate thescelosaurid specimen has been recovered from the formation.
In a 2001 review of hadrosaur eggshell and hatchling material from the Dinosaur Park Formation, Darren H. Tanke and M. K. Brett-Surman concluded that hadrosaurs nested in both the ancient upland and lowlands of the formation's depositional environment.[29] The upland nesting grounds may have been preferred by the less common hadrosaurs, like Brachylophosaurus or Parasaurolophus. However, the authors were unable to determine what specific factors shaped nesting ground choice in the formation's hadrosaurs. They suggested that behavior, diet, soil condition, and competition between dinosaur species all potentially influenced where hadrosaurs nested.[30]
Sub-centimeter fragments of pebbly-textured hadrosaur eggshell have been reported from the Dinosaur Park Formation. This eggshell is similar to the hadrosaur eggshell of Devil's Coulee in southern Alberta as well as that of the Two Medicine and Judith River Formations in Montana, United States.[31] While present, dinosaur eggshell is very rare in the Dinosaur Park Formation and is only found in two different microfossil sites.[29] These sites are distinguished by large numbers of pisidiid clams and other less common shelled invertebrates like unionid clams and snails. This association is not a coincidence as the invertebrate shells would have slowly dissolved and released enough basic calcium carbonate to protect the eggshells from naturally occurring acids that otherwise would have dissolved them and prevented fossilization.[31]
In contrast with eggshell fossils, the remains of very young hadrosaurs are actually somewhat common. Darren Tanke has observed that an experienced collector could actually discover multiple juvenile hadrosaur specimens in a single day. The most common remains of young hadrosaurs in the Dinosaur Park Formation are dentaries, bones from limbs and feet, as well as vertebral centra. The material showed little or none of the abrasion that would have resulted from transport, meaning the fossils were buried near their point of origin.[32] Bonebeds 23, 28, 47, and 50 are productive sources of young hadrosaur remains in the formation, especially bonebed 50. The bones of juvenile hadrosaurs and fossil eggshell fragments are not known to have preserved in association with each other, despite both being present in the formation.[33]
| Ornithopods from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
| Corythosaurus | C. casuarius | Lower-Middle, 76.5-75.5Ma ago[12] | "Approximately [ten] articulated skulls and associated postcrania, [ten to fifteen] articulated skulls, isolated skull elements, juvenile to adult."[34] | A lambeosaurin lambeosaurine hadrosaur | ||
| Gryposaurus | G. notabilis | Lower, 76.2-76Ma ago[12] | "Approximately [ten] complete skulls, [twelve] fragmentary skulls, associated postcrania."[35] | A kritosaurin saurolophine hadrosaur | ||
| Lambeosaurus | L. lambei | Upper, 75.5-75Ma ago[12] | "Approximately [seven] articulated skulls with associated postcrania, [possibly ten] articulated skulls, isolated skull elements, juvenile to adult."[36] | |||
| L. magnicristatus | Upper/Bearpaw Formation, 74.8Ma ago[12] | "[Two] complete skulls, one with associated, articulated postcrania."[36] | ||||
| Parasaurolophus | P. walkeri | Lower, 76.5-75.3Ma ago[8] | "Complete skull and postcranial skeleton."[36] | A parasaurolophin lambeosaurine hadrosaur. | ||
| Prosaurolophus | P. maximus | Upper, 75.5 – 74.8 Ma | "[Twenty to twenty-five] individuals, including at least [seven] articulated skulls and associated postcrania."[35] | A saurolophin saurolophine hadrosaur. | ||
Pachycephalosaurs
| Pachycephalosaurs from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
|
F. brevis |
Also present in the Oldman Formation |
Frontoparetal dome, various other skull fragments including juvenile and subadult material |
Once thought to be a species of Stegoceras |
|||
|
G. albertae |
"Frontoparietal dome."[37] |
Potentially synonymous with Stegoceras validum.[38] |
| |||
|
H. sternbergi |
Lower, also present in the Oldman Formation and Judith River Formation |
Potentially synonymous with Stegoceras validum.[38] |
| |||
|
S. lyonsi[39] |
Upper, 76.10 ± 0.5 Ma[39] |
Right squamosal[39] |
||||
|
S. validum |
Specimens including frontoparietal dome.[37] |
| ||||
|
A nomen nudum. |
||||||
Theropods
In the Dinosaur Park Formation, small theropods are rare due to the tendency of their thin-walled bones to be broken or poorly preserved.[40] Small bones of small theropods that were preyed upon by larger ones may have been swallowed whole and digested.[41] In this context, the discovery of a small theropod dinosaur with preserved tooth marks was especially valuable.[40] Possible indeterminate avimimid remains are known from the formation.
Ornithomimids
| Ornithomimids from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
| Ornithomimus | O. sp.[42] | Type specimen | An ornithomimid, possibly a species of Struthiomimus.[43] | |||
| Qiupalong | Q. sp.[44] | Several specimens | An ornithomimid, possibly a radiation of this genus from Asia.[44] | |||
| Rativates | R. evadens | Type specimen | An ornithomimid, formerly a specimen of Struthiomimus.[45] | |||
Oviraptorosaurs
| Oviraptorosaurs from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
| Caenagnathus | C. collinsi | Mandible, type specimen | A caenagnathid[46] which rivalled Anzu in size.[47] | |||
| Chirostenotes | C. pergracilis | Several fragmentary specimens, type specimen | A mid-sized caenagnathid. | |||
| Citipes | C. elegans[47] | Several fragmentary specimens, type specimen | Smallest caenagnathid from the formation.[47] | |||
| Macrophalangia | M. canadensis | Junior synonym of Chirostenotes pergracilis | ||||
Paravians
A new taxon of troodontid based solely on teeth is known from the upper part of the formation.[48]
| Paravians from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
| cf. Baptornis | Indeterminate | A hesperornithine bird | ||||
| cf. Cimolopteryx | Indeterminate | Partial coracoid | A possible charadriiform bird | |||
| Dromaeosaurus | D. albertensis | Several specimens and teeth, type specimen | A dromaeosaurid | |||
| Hesperonychus | H. elizabethae | Hip bones and partial toes and claws, type specimen | A dromaeosaurid or an avialan,[49][50] also found in the Oldman Formation | |||
| Latenivenatrix | L. mcmasterae | Hip bones, pelvis, skull fragments, type specimen | A large troodontid measuring Script error: No such module "convert".. | |||
| cf. Palintropus | Unnamed | Partial shoulder girdles | An ambiortiform bird | |||
| cf. Paronychodon | cf. P. lacustris | Teeth | An indeterminate maniraptoran, also found in the Judith River | |||
| cf. Pectinodon[51] | Indeterminate | Teeth | A troodont | |||
| Polyodontosaurus | P. grandis | Dentary, type specimen | Nomen dubium. Possibly synonymous with Latenivenatrix. | |||
| Richardoestesia | R. gilmorei | Mandible, type specimen | A dromaeosaurid | |||
| R. isosceles[48] | Teeth | |||||
| Saurornitholestes | S. langstoni | Incomplete skeleton and teeth, type specimen. A dentary referred to Saurornitholestes was discovered that preserved tooth marks left by a young tyrannosaur.[52] | A dromaeosaurid | |||
| Stenonychosaurus | S. inequalis | Nearly complete skeleton and other partial skeletons, type specimen | A troodontid once thought to be a species of Troodon | |||
Tyrannosaurs
| Tyrannosaurs from the Dinosaur Park Formation | ||||||
|---|---|---|---|---|---|---|
| Genus | Species | Location | Stratigraphic position | Material | Notes | Images |
| Daspletosaurus | D. wilsoni[53] | Middle-Upper, ~75 Ma ago[12] | Several specimens | A tyrannosaurine tyrannosaurid, also present in the Bearpaw Formation. | File:FMNH Daspletosaurus.jpg | |
| Gorgosaurus | G. libratus | Lower-Middle, 76.5–75 Ma ago[12] | Numerous specimens, type specimen[54] | An albertosaurine tyrannosaurid whose fossils have been unearthed in the Judith River Formation and possibly the Two Medicine Formation. It was the most common large carnivore in the area.[55] | ||
Other reptiles
Color key
|
Notes Uncertain or tentative taxa are in small text; |
Choristoderes
Choristoderes, or champsosaurs, were aquatic reptiles. Small examples looked like lizards, while larger types were superficially similar to crocodilians. Remains of the following Choristoderes have been found in the formation:[56]
- Champsosaurus (at least 3 species)
- Cteniogenys sp. cf. antiquus (possibly another genus)
Crocodylians
Remains of the following Crocodylians have been found in the formation:[57]
- Albertochampsa
- Leidyosuchus
- at least 1 unnamed taxon
Lizards
Remains of the following lizards have been found in the formation:[58]
Plesiosaurs
Remains of the following Plesiosaurs have been found in the formation:[59]
- Fluvionectes
- indeterminate polycotylids (shorter-necked)
Pterosaurs
Remains of the following pterosaurs have been found in the formation:[60]
- Cryodrakon [61] (known from small and large specimens)
- 1 unnamed non-azhdarchid pterosaur
Turtles
Remains of the following turtles have been found in the formation:[62]
- Adocus
- "Apalone"
- Aspideretoides (3 species)
- Basilemys
- Boremys
- Judithemys
- Neurankylus
- Plesiobaena
- 2 indeterminate taxa
Mammals
Remains of the following mammals have been found in the formation:[63]
- Multituberculata
- Cimexomys sp.
- Cimolodon spp.
- Cimolomys clarki
- Meniscoessus major
- Mesodma primaeva
- unnamed multituberculates
- Metatherians
- Alphadon halleyi
- Eodelphis browni
- E. cutleri
- 5 species of "Pediomys"
- Turgidodon russelli
- T. praesagus
- Eutherians
- Cimolestes sp. (uncertain taxonomy)
- Gypsonictops lewisi
- Paranyctoides sternbergi
- Unknown therians: at least 1 species
Fish
Remains of the following fish have been found in the formation:[64]
- Chondrichthyans
- Cretorectolobus olsoni (a carpet shark)
- Eucrossorhinus microcuspidatus (a carpet shark)
- Ischyrhiza mira (a sclerorhynchid)[65]
- Meristodonoides montanensis (a shark)
- Myledaphus bipartitus (a ray)
- Protoplatyrhina renae (a guitarfish)
- indeterminate orectolobid
- Acipenseriformes (sturgeons)
- "Acipenser albertensis"
- Anchiacipenser acanthaspis[66]
- unnamed sturgeon
- unnamed paddlefish
- Holostean fish
- Lepisosteus occidentalis (the gar)
- unnamed bowfin
- at least 2 other holosteans
- Teleost fish
- Archaeosiilik sp. (a pike)[67]
- Belonostomus longirostris
- Cretophareodus alberticus (an osteoglossomorph)
- Coriops amnicolus
- Estesesox foxi (a pike)
- Horseshoeichthys armaserratus (an ellimmichthyiform)[67]
- Nunikuluk gracilis (a pike)[67]
- Oldmanesox canadensis (a pike)
- Paralbula (including Phyllodus)
- Paratarpon apogerontus (an elopomorph, like the tarpon)
- Primuluchara laramidensis (a characin)[68][69]
- Sivulliusalmo sp. (a salmonid)[67]
- at least 8 other teleosts
Invertebrates
Remains of the following invertebrates have been found in the formation:[70]
- Freshwater bivalves
- Freshwater gastropods
- Campeloma (2 species)
- Elimia
- Goniobasis (3 species)
- Hydrobia
- Lioplacodes (2 species)
Flora
Plant body fossils
The following plant body fossils have been found in the formation:[71]
- various ferns
- Equisetum (Equisetaceae)
- Gymnosperms
- Platyspiroxylon (Cupressaceae)
- Podocarpoxylon (Podocarpaceae)
- Elatocladus (Taxodiaceae)
- Sequoia (Taxodiaceae)
- Sequoiaxylon (Taxodiaceae)
- Taxodioxylon (Taxodiaceae)
- Ginkgos
- Angiosperms
Palynomorphs
Palynomorphs are organic-walled microfossils, like spores, pollen, and algae. The following palynomorphs have been found in the formation:[72]
- Unknown producers
- at least 8 species
- Fungi
- at least 35 taxa
- Chlorophyta (green algae and blue-green algae)
- at least 12 species
- Pyrrhophyta (dinoflagellates, a type of marine algae)
- unassigned cysts
- Bryophytes (mosses, liverworts, and hornworts)
- Anthocerotophyta (hornworts)
- at least 5 species
- Marchantiophyta (liverworts)
- at least 14 species
- Bryophyta (mosses)
- at least 5 species
- Anthocerotophyta (hornworts)
- Lycopodiophyta
- Lycopodiaceae (club mosses)
- at least 11 species
- Selaginellaceae (small club mosses)
- at least 6 species
- Isoetaceae (quillworts)
- at least 1 species
- Lycopodiaceae (club mosses)
- Polypodiophyta
- Osmundaceae (cinnamon ferns)
- at least 6 species
- Schizaeaceae (climbing ferns)
- at least 20 species
- Gleicheniaceae (Gleichenia and allies; coral ferns)
- at least 5 species
- Cyatheaceae (Cyathea and allies)
- at least 4 species
- Dicksoniaceae (Dicksonia and allies)
- at least 3 species
- Polypodiaceae (ferns)
- at least 4 species
- Matoniaceae
- at least 1 species
- Marsileaceae
- at least 1 species
- Osmundaceae (cinnamon ferns)
- Pinophyta (gymnosperms)
- Cycadaceae (cycads)
- at least 3 species
- Caytoniaceae
- at least 1 species
- Pinaceae (pines)
- at least 4 species
- Cupressaceae (cypresses)
- at least 3 species
- Podocarpaceae (Podocarpus and allies)
- at least 4 species
- Cheirolepidiaceae
- at least 2 species
- Ephedraceae (Mormon teas)
- at least 6 species
- Unknown gymnosperms: at least 3 species
- Cycadaceae (cycads)
- Magnoliophyta (angiosperms)
- Magnoliopsida (dicots)
- Buxaceae (boxwood)
- at least 1 species
- Gunneraceae (gunneras)
- at least 1 species
- Salicaceae (willows, cottonwood, quaking aspen)
- at least 1 species
- Droseraceae (sundews)
- at least 1 species
- Olacaceae (tallowwood)
- at least 2 species
- Loranthaceae (showy mistletoes)
- at least 1 species
- Sapindaceae (soapberry)
- at least 1 species
- Aceraceae (maples)
- at least 1 species
- Proteaceae (proteas)
- at least 9 species
- Compositae (sunflowers)
- at least 1 species
- Fagaceae (beeches, oaks, chestnuts)
- at least 2 species
- Betulaceae (birches, alders)
- at least 1 species
- Ulmaceae (elms)
- at least 1 species
- Chenopodiaceae (goosefoots)
- at least 1 species
- Buxaceae (boxwood)
- Liliopsida (monocots)
- Liliaceae (lilies)
- at least 6 species
- Cyperaceae (sedges)
- at least 1 species
- Sparganiaceae (bur-reeds)
- possibly 1 species
- Unknown angiosperms: at least 88 species
- Liliaceae (lilies)
- Magnoliopsida (dicots)
See also
Footnotes
References
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- ↑ Script error: No such module "Citation/CS1".
- ↑ a b c d Eberth, D.A. 2005. The geology. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p.54-82. Template:ISBN.
- ↑ Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 277-291. Template:ISBN.
- ↑ a b Cite error: Script error: No such module "Namespace detect".Script error: No such module "Namespace detect".
- ↑ Script error: No such module "citation/CS1".
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- ↑ Ryan and Evans (2005).
- ↑ a b Script error: No such module "Citation/CS1".Script error: No such module "Unsubst".
- ↑ Gardner, J.D. 2005. Lissamphibians. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 186-201. Template:ISBN.
- ↑ Script error: No such module "citation/CS1".
- ↑ Script error: No such module "citation/CS1".
- ↑ a b c d e f g h i j k l Script error: No such module "Citation/CS1".
- ↑ Currie, P.J. 2005. Theropods, including birds. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 367-397. Template:ISBN.
- ↑ Ryan, M.J., and Evans, D.C. 2005. Ornithischian dinosaurs. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 312-348. Template:ISBN.
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- ↑ a b c "Table 23.1," in Weishampel, et al. (2004). Page 495.
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- ↑ a b "Abstract," Tanke and Brett-Surman (2001). Page 206.
- ↑ "Conclusions," Tanke and Brett-Surman (2001). Page 212.
- ↑ a b "Eggshell," Tanke and Brett-Surman (2001). Page 209.
- ↑ "Introduction," Tanke and Brett-Surman (2001). Page 208.
- ↑ "Discussion," Tanke and Brett-Surman (2001). Page 212.
- ↑ "Table 20.1," in Weishampel, et al. (2004). Page 441.
- ↑ a b "Table 20.1," in Weishampel, et al. (2004). Page 440.
- ↑ a b c "Table 20.1," in Weishampel, et al. (2004). Page 442.
- ↑ a b "Table 21.1," in Weishampel, et al. (2004). Page 465.
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- ↑ a b "Introduction," Jacobsen (2001). Page 59.
- ↑ "Discussion," Jacobsen (2001). Page 61.
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- ↑ "Abstract," Jacobsen (2001). Page 58.
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- ↑ K.Gao and Brinkman, D.B. 2005. Choristoderes from the Park and its vicinity. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 221-234. Template:ISBN.
- ↑ Xiao-Chun Wu. 2005. Crocodylians. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 277-291. Template:ISBN.
- ↑ Caldwell, M.W. The squamates: origins, phylogeny, and paleoecology. In: Currie, P.J., and Koppelhus, E.B. (eds). 2005. Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 235-248. Template:ISBN.
- ↑ Sato, T., Eberth, D.A., Nicholls, E.L., and Manabe, M. 2005. Plesiosaurian remains from non-marine to paralic sediments. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 249-276. Template:ISBN.
- ↑ Godfrey, S.J., and Currie, P.J. 2005. Pterosaurs. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 292-311. Template:ISBN.
- ↑ Script error: No such module "Citation/CS1".
- ↑ Brinkman, D.B. 2005. Turtles: diversity, paleoecology, and distribution. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 202-220. Template:ISBN.
- ↑ Fox, R.C. 2005. Late Cretaceous mammals. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 417-435. Template:ISBN.
- ↑ Neuman, A.G., and Brinkman, D.B. 2005. Fishes of the fluvial beds. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 167-185. Template:ISBN.
- ↑ Script error: No such module "citation/CS1".
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- ↑ Johnston, P.A., and Hendy, A.J.W. 2005. Paleoecology of mollusks from the Upper Cretaceous Belly River Group. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 139-166. Template:ISBN.
- ↑ Koppelhus, E.B. 2005. Paleobotany. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 131-138. Template:ISBN.
- ↑ Braman, D.R., and Koppelhus, E.B. 2005. Campanian palynomorphs. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, p. 101-130. Template:ISBN.
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- Brinkman, D.B. 2005. Turtles: diversity, paleoecology, and distribution. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, 202–220.
- Caldwell, M.W. The squamates: origins, phylogeny, and paleoecology. In: Currie, P.J., and Koppelhus, E.B. (eds). 2005. Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, 235–248.
- Currie, P.J. 2005. Theropods, including birds. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, 367–397.
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- K. Gao and Brinkman, D.B. 2005. Choristoderes from the Park and its vicinity. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, 221–234.
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- Sato, T., Eberth, D.A., Nicholls, E.L., and Manabe, M. 2005. Plesiosaurian remains from non-marine to paralic sediments. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, 249–276.
- Tanke, D.H. and Brett-Surman, M.K. 2001. Evidence of Hatchling and Nestling-Size Hadrosaurs (Reptilia:Ornithischia) from Dinosaur Provincial Park (Dinosaur Park Formation: Campanian), Alberta, Canada. pp. 206–218. In: Mesozoic Vertebrate Life—New Research Inspired by the Paleontology of Philip J. Currie. Edited by D.H. Tanke and K. Carpenter. Indiana University Press: Bloomington. xviii + 577 pp.
- Xiao-Chun Wu. 2005. Crocodylians. In: Currie, P.J., and Koppelhus, E.B. (eds), Dinosaur Provincial Park: A Spectacular Ancient Ecosystem Revealed. Indiana University Press: Bloomington and Indianapolis, 277-291