Allenby Formation
There are several notable fossil producing localities in the Princeton & Tulameen basins. Historical collection sites included Nine Mile Creek, Vermilian Bluffs, and Whipsaw Creek, while modern sites include One Mile Creek, Pleasant Valley, Thomas Ranch, and the Princeton Chert.
Extent and correlation
The Allenby is estimated to have an overall extent of approximately 300 km (120 sq mi), though actual outcroppings of the formation make up less than 1% of the formation, while other exploratory contact is via boreholes and mines. The half-graben which contains the formation is separated into two major depositional basins, the Princeton basin around Princeton, British Columbia and the Tulameen basin centered approximately 17 km (11 mi) west. The grabens extensional faults at the eastern side of the basin place the hanging wall Allenby strata in contact with much older foot wall strata of the Nicola Formation which dates to the Upper Triassic.
The Allenby Formation is the southern-most of the Eocene Okanagan Highlands lakes in British Columbia, and second most southern site after the Klondike Mountain Formation of Republic, Washington and northern Ferry County. In British Columbia, the formation is coeval to the Tranquille Formation, known from the McAbee Fossil Beds and Falkland site, the Coldwater Beds, known from the Quilchena site, and Driftwood Canyon Provincial Park. The highlands, including the Allenby Formation, have been described as one of the "Great Canadian Lagerstätten" based on the diversity, quality and unique nature of the biotas that are preserved. The highlands temperate biome preserved across a large transect of lakes recorded many of the earliest appearances of modern genera, while also documenting the last stands of ancient lines.
The warm temperate uplands floras of the Allenby Formation and the highlands, associated with downfaulted lacustrine basins and active volcanism are noted to have no exact modern equivalents, due to the more seasonally equitable conditions of the Early Eocene. However, the formation has been compared to the upland ecological islands in the Virunga Mountains within the Albertine Rift of the African rift valley.
The earliest work in the region was on exploratory expeditions in 1877 and 1878, with fossils collected in the areas of Nine-Mile Creek, Vermilian Bluffs on the Similkameen River, and Whipsaw Creek. While reporting on additional plant fossils collected from British Columbia, Penhallow (1906) noted the likely coeval status of the Princeton basins with many of the sites now considered the Okanagan Highlands. Modern collecting has centered on the areas around One Mile Creek, Pleasant Valley, and Thomas Ranch.
Age
The age estimates for the Allenby Formation have varied a number of times since the first explorations happened in the 1870s. Shaw (1952) dated the formation as Oligocene, an age followed by Arnold (1955). Half a decade later, the older age of 48 ± 2 million years old was first suggested, with a younger age being suggested at 46.2 ± 1.9 million years old in 2000 and an older date of 52.08 ± 0.12 million years ago obtained from uranium–lead dating of zircons from Vermilion Bluffs shale in 2005.
Lithology
The Allenby is composed of cyclical sedimentation events that were deposited along the course of a river-system in conjunction with depositional areas from nearby lakes and wetlands. Coeval volcanic eruptive events are recorded as interbeds of tephras and lavas, while the riverine course is marked with depositional areas of conglomerates and sandstones. The quieter environments are noted for finer layers of shales and coalified layers.
The coal seams throughout the formation are typically sub-bituminous.
Notable in conjunction with the coal seams are sections of chert which formed during silica rich periods. The rapid cyclical changes from coal to chert and back are not noted in any other fossil locality in the world. An estimated 49 coal-chert cycles are known, though the exact conditions for this process are not well understood. Silica rich volcanic episodes in the region during deposition would have been needed for formation of the cherts, while slowly moving waters and gently subsiding terrains would be needed for the peats and fens to accumulate. Rates of organic deposition in swamps have been estimated at 0.5–1 mm (0.020–0.039 in) in modern temperate climates, this suggests the time needed for each 10–20 cm (3.9–7.9 in) chert layer would be at least 100 years or more, with the full sequence of cycles taking place over no more than 15,000 years.
Palynoflora
Palynological analysis of samples from the Thomas ranch site by Dillhoff et al. (2013) resulted in the identification of 32 pollen and spore types that were assignable to family or genus level, with a total number of distinct pollen and spore types, including unassignable morphotypes, number over 70. The predominant pollens of the site are conifers, which make up between 85%–97% of the total pollens, while the angiosperm pollens are dominated by members of Betulaceae.
Several pteridophyte families and genera are represented as spore fossils alone, without corresponding megafossil records, including Lycopodiaceae, Osmundaceae, and Schizaeaceae. Similarly, at least three additional conifer genera are only present as pollen fossils and up to 12 angiosperms are present in the pollen record. Sometimes considered a Biostratgraphic index fossil, the angiosperm palynospecies Pistillipollenites macgregorii has been recovered from several sites in the Allenby Formation, while the palynospecies Erdtmanipollis pachysandroides is rare, having only been reported from the formation twice.
Family | Genus | Species | Pollen/Macrofossil | Notes | Images |
---|---|---|---|---|---|
Unidentified |
Pollen |
A holly palynomorph |
|||
Pollen |
A palm palynomorph |
||||
Pollen |
A box family palynomorph |
||||
Unidentified |
Pollen & macrofossils |
An alder palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A birch palynomorph |
|||
Unidentified |
Pollen |
A hornbeam palynomorph |
|||
unidentified |
Pollen |
A hazelnut palynomorph |
|||
unidentified |
Pollen |
A Cunninghamia like palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A redwood palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A Taxodioideae subfamily palynomorph |
|||
Unidentified |
Pollen |
An elaeagnaceous palynomorph, similar to oleaster |
|||
unidentified |
Unidentified |
Pollen |
An ericaceous palynomorph of uncertain affinity |
||
Unidentified |
Pollen |
A chestnut palynomorph |
|||
Unidentified |
Pollen |
A fagaceous palynomorph |
|||
"Fagus Pollen type 3" |
Pollen |
A beech palynomorph |
|||
"Fagus Pollen type 2" |
Pollen |
A beech palynomorph |
|||
Pollen |
A fagaceous palynomorph |
||||
"Quercus Pollen type 1" |
Pollen |
An oak palynomorph, similar to Quercus Group Lobatae pollen |
|||
"Quercus Pollen type 2" |
Pollen |
An oak palynomorph, ancestral type with Quercus Group Ilex morphology |
|||
Unidentified |
Pollen |
A fagaceous palynomorph |
|||
Unidentified |
Unidentified |
Pollen |
A Fagoideceous palynomorph |
||
Unidentified |
Pollen |
||||
Pollen & macrofossils |
A Gingko palynomorph |
||||
Unidentified |
Pollen |
A sweet gum palynomorph |
|||
Unidentified |
Pollen |
A hickory palynomorph |
|||
Unidentified |
Pollen |
A hickory palynomorph |
|||
Unidentified |
Pollen |
A lycopod palynomorph |
|||
Unidentified |
Pollen |
A linden palynomorph |
|||
Unidentified |
Pollen |
An osmundaceous fern palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A fir palynomorph |
|||
Unidentified |
Pollen |
A pine family palynomorph |
|||
Unidentified |
Pollen |
A Picea palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A Pinus palynomorph |
|||
Unidentified |
Pollen |
A pine family palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A Pseudolarix palynomorph |
|||
Unidentified |
Pollen |
A Tsuga palynomorph |
|||
Unidentified |
Pollen |
A Laricoidae palynomorph, similar to larch |
|||
Unidentified |
Pollen |
A Laricoidae palynomorph, similar to pseudotsuga |
|||
Unidentified |
Pollen |
A Platanus palynomorph |
|||
Unidentified |
Pollen |
A Potamogeton palynomorph |
|||
Unidentified |
Unidentified |
Pollen & macrofossils |
Rose famnily palynomorphs |
||
Unidentified |
Pollen |
A willow palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A duck weed palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A maple palynomorph |
|||
Unidentified |
Pollen & macrofossils |
A horse chestnut palynomorph |
|||
Unidentified |
Unidentified |
Pollen |
A sapotaceous palynomorph |
||
Unidentified |
Pollen |
A yew palynomorph |
|||
Unidentified |
Pollen & macrofossils |
An elm palynomorph |
|||
Pollen |
A palynomorph of uncertain affinity, possibly a Gentianaceae or Euphorbiaceae species |
Compression paleobiota
A group of six mosses were described from the Allenby Formation by Kuc (1972, 1974) representing the genera Ditrichites, Hypnites and Plagiopodopsis, with two species placed in the morphogenus Muscites. Dillhoff et al. (2013) identified twelve distinct gymnosperm taxa spanning the families Cupressaceae, Ginkgoaceae, and Pinaceae. While being the minority component of the Thomas Ranch flora by total fossil numbers, angiosperms have a higher diversity, with 45 distinct morphotypes represented as foliage, reproductive structures, or both. Seventeen of the morphotypes are identifiable to genus or species, with members of the family Betulaceae being most prominent. At least common one leaf type is suggested to possibly represent an extinct plant order, but has not been described. Only two pteridophyte species have been described from the compression flora, Azolla primaeva by Penhallow (1890) and Equisetum similkamense by Dawson (1878).
The following fossil conifers, pteridophytes, ginkgophytes and bryophytes have been described from the Allenby Formation:
Bryophytes
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
(Kuc) Miller |
An amblystegiaceous moss |
||||
(Kuc) Miller |
An amblystegiaceous moss |
||||
(Kuc) Miller |
A bartramiaceous moss |
||||
Kuc |
|||||
incertae sedis |
Kuc |
A moss of uncertain placement |
|||
incertae sedis |
Kuc |
A moss of uncertain placement |
Pteridophytes
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
A mosquito fern |
Gingkophytes
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
A ginkgo |
|||||
Mustoe, 2002 |
A ginkgo with highly dissected leaves |
Pinophytes
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
(Lesquereux) MacGinitie |
|||||
First identified as "Sequoia" brevifolia, "S." heeri. "S." langsdorfii (in part), "S." nordenskiöldi, & Taxodium distichum miocenum (in part) |
|||||
Lesquereux |
A redwood |
||||
First identified as "Sequoia" angustifolia, |
|||||
Oldest true fir described |
|||||
Undescribed |
A spruce |
||||
A pinaceous winged seed |
|||||
Dawson, 1890 |
|||||
(J.Nelson) Rehder |
Originally identified as Pseudolarix americana, then as Pseudolarix arnoldii |
||||
Gooch |
Angiosperms
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Wolfe & Wehr |
A sumac |
||||
Pigg, Bryan, & DeVore |
An onion relative |
||||
(Berry) Wolfe & Wehr |
An Alder |
||||
Wolfe & Wehr |
A birch |
||||
Pigg, Manchester, & Wehr |
A coryloid genus |
||||
(Dawson) Wolfe & Wehr |
A katsura |
||||
(Knowlton) Wolfe & Wehr |
A beech |
||||
Undescribed |
A beech species Not described to species | ||||
Undescribed |
A gooseberry species |
||||
Radtke, Pigg & Wehr |
A winter-hazel species |
||||
Undescribed |
A wingnut |
||||
Undescribed |
A laural species |
||||
Berry |
A laural species |
||||
Undescribed |
An extinct sterculioid flower |
||||
Wolfe & Wehr |
A dove-tree relative |
||||
Undescribed |
Manchester |
A sycamore morphospecies |
|||
(Lesquereux) Wolfe & Wehr |
A sycamore |
||||
Unidentified |
A service berry |
||||
A snow wreath |
|||||
A Sorbarieae genus |
|||||
Wolfe & Tanai |
A maple |
||||
Wolfe & Tanai |
A maple |
||||
Wolfe & Tanai |
A maple |
||||
Wolfe & Tanai |
A maple |
||||
Wolfe & Tanai |
A maple |
||||
Wolfe & Tanai |
A maple |
||||
Wolfe & Tanai |
A maple |
||||
McClain and Manchester |
A Dipteronia species |
||||
Pigg et al. |
A Tetracentron relative |
||||
Undescribed |
A trochodendraceous species |
||||
Denk & Dillhoff |
An elm |
||||
Undescribed |
|||||
(Lesquereux) Wang & Manchester |
A sapindalean flower of uncertain affiliations |
Mollusks
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
L.S. Russell, 1957 |
A hydrobiid mud snail |
||||
L.S. Russell, 1957 |
A lymnaeine pond snail |
||||
L.S. Russell, 1957 |
An aplexine bladder snail |
||||
L.S. Russell, 1957 |
A physine bladder snail |
||||
L.S. Russell, 1957 |
An ancylinine ramshorn snail |
||||
Indeterminate |
L.S. Russell, 1957 |
A possible planorbinine ramshorn snail |
|||
Indeterminate |
L.S. Russell, 1957 |
A possible sphaeriine fingernail clam |
Insects
Coleopterans
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Unidentified |
Unidentified |
A soldier beetle |
|||
Unidentified |
Unidentified |
A caraboid superfamily beetle |
|||
Scudder, 1895 |
|||||
Scudder, 1879 |
|||||
Scudder, 1879 |
|||||
Undescribed |
Scudder, 1895 |
A click beetle |
|||
Scudder, 1895 |
|||||
Scudder, 1879 |
|||||
Scudder, 1879 |
Dipterans
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Rice, 1959 |
A marchfly |
||||
Rice, 1959 |
A marchfly |
||||
(Handlirsch, 1910) |
A marchfly |
||||
(Handlirsh, 1910) |
A marchfly |
||||
(Handlirsch, 1910) |
A marchfly |
||||
(Handlirsch, 1910) |
A marchfly |
||||
(Handlirsch, 1910) |
A marchfly |
||||
Rice, 1959 |
A marchfly |
||||
(Handlirsh, 1910) |
A marchfly |
||||
(Handlirsh, 1910) |
A marchfly Penthetria lambei (1910), Penthetria ovalis (1910), & Penthetria separanda (1910) considered junior synonyms (1959) |
||||
(Handlirsch, 1910) |
A marchfly |
||||
(Handlirsh, 1910) |
A marchfly |
||||
(Handlirsh, 1910) |
A marchfly |
||||
(Scudder, 1879) |
A marchfly |
||||
(Handlirsh, 1910) |
A marchfly |
||||
Rice, 1959 |
A marchfly |
||||
(Handlirsch, 1910) |
A long-legged fly |
||||
Handlirsh, 1909 |
|||||
(Handlirsh, 1910) |
A cranefly |
Hemipterans
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Handlirsch, 1910 |
|||||
Scudder, 1895 |
|||||
Undescribed |
Scudder, 1895 |
A spittlebug |
|||
Scudder, 1895 |
|||||
Scudder, 1895 |
|||||
Scudder, 1879 |
|||||
Scudder, 1895 |
|||||
Scudder, 1895 |
|||||
Undescribed |
Scudder, 1895 |
A froghopper |
|||
Scudder, 1895 |
|||||
Scudder, 1895 |
|||||
Scudder, 1879 |
|||||
Undescribed |
Scudder, 1895 |
A fulgorid plant hopper |
|||
(Scudder, 1879) |
A gerrine water strider moved to Telmatrechus stali (1895) |
||||
Scudder, 1879 |
A hemipteran of uncertain placement |
Hymenopterans
Archibald, Mathewes, & Aase (2023) reported a Titanomyrma species ant queen from the Vermillion Bluffs site, and noted the range extension for Formiciinae into the highlands, as the subfamily was previously considered a strictly thermophilic ant group. Due to complications arising from preservational distortion during diagenesis, they were unable to determine the correct size of the queen in life. If the distortion was lateral, then compression to bilateral symmetry yielded an adult length of approximately 3.3 cm (1.3 in), placing it the same range as Formicium berryi and F. brodiei, known only from wings, and sugg4ested as possible males. Conversely stretching the fossil to bilateral symmetry results in a larger 5 cm (2.0 in) length estimate, placing it as comparable to queens of T. lubei and T. simillima.
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Undescribed |
A braconid wasp |
||||
Indeterminate |
A formiciine titan ant |
||||
(Handlirsch, 1910) |
A xoridine ichneumon parasitic wasp |
||||
Rice, 1968 |
Mecopterans
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Archibald, 2005 |
|||||
Archibald & Rasnitsyn, 2018 |
Neuropterans
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
(Scudder, 1895) |
A Polystoechotid-group giant lacewing |
Odonata
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Indeterminate |
Indeterminate |
A daner dragonfly |
|||
Archibald & Cannings, 2022 |
A possible Dysagrionidae odonate. |
Raphidiopterans
Family | Genus | Species | Authority | Notes | Images |
---|---|---|---|---|---|
Archibald & Makarkin, 2021 |
Vertebrates
Family | Genus | Species | Authors | Notes | Images |
---|---|---|---|---|---|
Wilson, 1982 |
A bowfin |
||||
Aves incertae sedis |
Unidentified |
Unidentified |
Mayr et al., 2019 |
Indeterminate feathers and a skeleton |
|
(Cope, 1893) |
A catostomid sucker |
||||
(Marsh, 1874) |
A tillodont species |
||||
(Hussakof, 1916) |
A mooneye |
||||
Wilson, 1977 |
A percopsiform fish |
||||
Wilson, 1977 |
An ancestral salmon |
||||
Undescribed |
A soft shelled turtle |
Princeton Chert biota
The Princeton chert biota is unique in the Allenby formation due to the silicification of the chert, which has resulted in cellular and anatomical preservation of the organisms. As of 2016 over 30 different plant taxa had been described from chert fossils along with a number of fungal species.
Fungi
Order | Genus | Species | Authors | Notes | Images |
---|---|---|---|---|---|
Currah, Stockey, LePage |
An ascomycetan fungus on the host palm Uhlia allenbyensis |
||||
Klymiuk |
An ascomycotan fungus |
||||
Currah, Stockey, LePage |
An ascomycetan fungus on the host palm Uhlia allenbyensis |
Ferns
Family | Genus | Species | Authors | Notes | Images |
---|---|---|---|---|---|
Karafit et al. |
|||||
Stockey, Nishida, & Rothwell |
|||||
Smith et al. |
|||||
Cevallos-Ferriz, Stockey, & Pigg |
|||||
Undescribed |
An osmundaceous fern |
Conifers
Family | Genus | Species | Authors | Notes | Images |
---|---|---|---|---|---|
Bassinger |
|||||
Stockey |
A 2-needled Pine foliage |
||||
Stockey |
A 3-needled Pine foliage |
||||
Miller |
A basal Pine |
||||
Stockey |
A pinaceous cone |
||||
Miller |
A basal Pine |
Angiosperms
Family | Genus | Species | Authors | Notes | Images |
---|---|---|---|---|---|
Erwin & Stockey |
An aquatic or emergent water-plantain |
||||
Grímsson, Zetter, & Halbritter |
A Cape-pondweed pollen |
||||
Cevallos-Ferriz & Stockey |
An arum family member |
||||
Erwin & Stockey |
|||||
Undescribed |
Cevallos-Ferriz |
A current fruit |
|||
Cevallos-Ferriz & Stockey |
|||||
Cevallos-Ferriz & Stockey |
A Liriodendron-like wood. |
||||
Pigg, Stockey & Maxwell |
A Myrtaceous fruit |
||||
Cevallos-Ferriz & Stockey |
A water lily relative |
||||
Stockey, LePage, & Pigg |
A tuplo relative. |
||||
Bassinger |
A rose family flower |
||||
Cevallos-Ferriz & Stockey |
A prunoid wood. |
||||
"Species 1" |
Cevallos-Ferriz & Stockey |
A prunoid seed. |
|||
"Species 2" |
Cevallos-Ferriz & Stockey |
A prunoid seed. |
|||
"Species 3" |
Cevallos-Ferriz & Stockey |
A prunoid seed. |
|||
Erwin & Stockey |
A possible dodonaecous soapberry family flower |
||||
Smith & Stockey |
A lizard's-tail species |
||||
Cevallos-Ferriz & Stockey |
A grape family fruit of uncertain generic placement |
||||
incertae sedis |
"Type 1" |
Cevallos-Ferriz & Stockey |
A grape family fruit of uncertain generic placement |
||
incertae sedis |
"Type 2" |
Cevallos-Ferriz & Stockey |
A grape family fruit of uncertain generic placement |
||
Zetter & Hesse |
A possible iridaceous pollen morphotype |
||||
Robison & Person |
A semi-aquatic dicot of uncertain affinity. |
||||
Erwin & Stockey |
A cyperaceous or juncaceous monocot |
||||
Stockey |
A possibly aquatic magnoliopsid flower of uncertain affiliation. |
||||
Erwin & Stockey |
A lilialean genus of uncertain placement |
References
- ^ Mustoe, G. (2010). "Cyclic sedimentation in the Eocene Allenby Formation of south-central British Columbia and the origin of the Princeton Chert fossil beds". Canadian Journal of Earth Sciences. 48 (1): 25–43. doi:10.1139/e10-085.
- ^ Dillhoff, R.M.; Dillhoff, T.A.; Greenwood, D.R.; DeVore, M.L.; Pigg, K.B. (2013). "The Eocene Thomas Ranch flora, Allenby Formation, Princeton, British Columbia, Canada". Botany. 91 (8): 514–529. doi:10.1139/cjb-2012-0313.
- ^ Greenwood, D.R.; Pigg, K.B.; Basinger, J.F.; DeVore, M.L. (2016). "A review of paleobotanical studies of the Early Eocene Okanagan (Okanogan) Highlands floras of British Columbia, Canada, and Washington, U.S.A." Canadian Journal of Earth Sciences. 53 (6): 548–564. Bibcode:2016CaJES..53..548G. doi:10.1139/cjes-2015-0177. hdl:1807/71961.
- ^ Archibald, S.; Greenwood, D.; Smith, R.; Mathewes, R.; Basinger, J. (2011). "Great Canadian Lagerstätten 1. Early Eocene Lagerstätten of the Okanagan Highlands (British Columbia and Washington State)". Geoscience Canada. 38 (4): 155–164.
- ^ DeVore, M. L.; Nyandwi, A.; Eckardt, W.; Bizuru, E.; Mujawamariya, M.; Pigg, K. B. (2020). "Urticaceae leaves with stinging trichomes were already present in latest early Eocene Okanogan Highlands, British Columbia, Canada". American Journal of Botany. 107 (10): 1449–1456. doi:10.1002/ajb2.1548. PMID 33091153. S2CID 225050834.
- ^ Penhallow, D.P. (1908). "A report on Tertiary plants of British Columbia, collected by Lawrence M. Lambe in 1906 together with a discussion of previously recorded Tertiary floras". Report 1013. Canada Department of Mines, Geological Survey Branch. pp. 1–167.
- ^ Shaw, W. S. (1952). "The Princeton Coalfield, British Columbia". Geological Survey of Canada.
- ^ Arnold, C. A. (1955). "A Tertiary Azolla from British Columbia" (PDF). Contributions from the Museum of Paleontology, University of Michigan. 12 (4): 37–45.
- ^ Grímsson, F.; Grimm, G.; Zetter, R.; Denk, T. (2016). "Cretaceous and Paleogene Fagaceae from North America and Greenland: evidence for a Late Cretaceous split between Fagus and the remaining Fagaceae". Acta Palaeobotanica. 56 (2): 247–305. doi:10.1515/acpa-2016-0016. S2CID 4979967.
- ^ Kuc, M. (1972). "Muscites eocenicus sp. nov.—a fossil moss from the Allenby Formation (middle Eocene), British Columbia". Canadian Journal of Earth Sciences. 9 (5): 600–602. Bibcode:1972CaJES...9..600K. doi:10.1139/e72-049.
- ^ Kuc, M. (1974). "Fossil mosses from the bisaccate zone of the mid-Eocene Allenby Formation, British Columbia". Canadian Journal of Earth Sciences. 11 (3): 409–421. Bibcode:1974CaJES..11..409K. doi:10.1139/e74-037.
- ^ Dawson, J. W. (1890). On fossil plants from the Similkameen Valley and other places in the southern interior of British Columbia. Royal Society of Canada.
- ^ Miller, N. G. (1980). "Fossil mosses of North America and their significance". The Mosses of North America. pp. 9–36.
- ^ Mustoe, G.E. (2002). "Eocene Ginkgo leaf fossils from the Pacific Northwest". Canadian Journal of Botany. 80 (10): 1078–1087. doi:10.1139/b02-097.
- ^ Arnold, C. A. (1955). "Tertiary conifers from the Princeton coal field of British Columbia" (PDF). University of Michigan: Contributions from the Museum of Paleontology. 12: 245–258.
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