The paleofauna of the Eocene Okanagan Highlands consists of Early Eocene arthropods, vertebrates, plus rare nematodes and molluscs found in geological formations of the northwestern North American Eocene Okanagan Highlands. The highlands lake bed series' as a whole are considered one of the great Canadian Lagerstätten . The paleofauna represents that of a late Ypresian upland temperate ecosystem immediately after the Paleocene-Eocene thermal maximum, and before the increased cooling of the middle and late Eocene to Oligocene. The fossiliferous deposits of the region were noted as early as 1873, with small amounts of systematic work happening in the 1880-90s on British Columbian sites, and 1920-30s for Washington sites. Focus and more detailed descriptive work on the Okanagan Highlands site started in the last 1970's. Most of the highlands sites are preserved as compression-impression fossils in "shales", but also includes a rare permineralized biota and an amber biota.
The 1,000 km (620 mi) series of lacustrine deposits are located across the Central British Columbia, Canada southeast to northern central Washington state, United States. grouped informally into "Northern", "Central", and "Southern" sites. [1] The Northern sites consist of unnamed Ootsa Group formations which outcrop as the "Driftwood shales" near Smithers, British Columbia, the "Horsefly shales", of an unnamed formation and unnamed group which outcrop around Horsefly, British Columbia, [1] and possibly sites now considered lost in the Quesnel, British Columbia area, [2] The Central sites represent Kamloops Group formations with the McAbee Fossil Beds, Tranquille River site and Falkland site, all in the Tranquille Formation, the Quichena site and Stump Lake site in the Coldwater Beds and outcrops of the Chu Chua Formation near Barriere, British Columbia. The Southern sites include the Princeton Group Allenby Formation sites surrounding Princeton, British Columbia, such as "Nine Mile Creek", "One Mile Creek", "Pleasant Valley", "Thomas Ranch", "Vermilian Bluffs", and "Whipsaw Creek". The Penticton Groups Kettle River, Marama and Marron Formations in the Boundary District along the Canada-United States border are closely correlated with the Klondike Mountain Formation across the border. [3] The most southerly of the Okanagan Highlands lakes, the Klondike Mountain Formation in Northern Ferry County, Washington include the "Boot Hill site", "Corner Lot site", "Gold Mountain site", "Knob Hill site", and "Mount Elizabeth site". [1]
There is debate as to the affiliation of the, potentially lost, Quesnel sites with the Greater Okanagan Highlands. Archibald et al. (2018) in a monograph of the Highlands Hymenoptera families included them as part of the series. [4] However the certainty for the placement was questioned earlier by Eberle et al. (2017) [5] and Archibald and Cannings (2022) who opted to tentatively exclude Quesnel from the highlands while discussing the history of field colleting in the region. [2]
The Okanagan highlands represent a snapshot of lake, wetlands, and montane forest animal life which existed approximately 15 million years ago after the Cretaceous–Paleogene extinction event. The temperate upland lakes hosted insects, fish, birds, and mammals with the notably well preserved megafossils often retaining insect colour patterns, gnat wing membrane hairs, and whole bird feathers. [6] In some cases the fine detail preservation of soft parts allows for the preservation of internal anatomy. [7]
Archibald and Makarkin (2006) suggested the disjunct distribution of genera between the Danish western Limfjord coasts Fur Formation and the Okanagan highlands may have been enabled by rising crust elevations in the northern Atlantic region and subsequent increase in landmass during the Late Paleocene which linked Northern Europe with Greenland until at least the Early Eocene. [8] Several land bridge routes may have acted as migration corridors for biotic interchange, the northern De Geer land bridge from Fennoscandia to North America via northern Greenland, and the southern Thulean land bridge from northern Britain though the Faroe Islands and then Greenland and North America. Several insect genera share disjunct distributions between the highlands and Limfjord including the mecopteran Cimbrophlebia , the giant lacewing Palaeopsychops , the green lacewing Protochrysa , the bull dog ant Ypresiomyrma . [8]
The Hat Creek Amber deposits in the central region provide evidence for small and microbiotic elements of the Okanagan Highlands forests though entombed organisms such at terrestrial nematodes and microwasps that otherwise would likely not be preserved in the lake environments. [9] The highlands as a whole have been described as one of the "Great Canadian Lagerstätten " [6] 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. [6] David Grimaldi et al. (2018) during discussion of inclusions in Alaskan Chickaloon amber, noted the Okanagan Highlands record of latitudinal extinctions, specifically the modern southern hemisphere endemic groups Eomeropidae mecopterans and Myrmeciinae bulldog ants. [10]
The majority of the lake deposits are compression fossils in lake bed sediments noted for both the paleofauna and paleofloras, with an additional pair of important non-compression biotas. A permineralized chert flora, the Princeton Chert is found along the Similkameen River interbedded with coal deposits of the Ashnola shale unit, Allenby Formation known for anatomically preserved plants. [11] In the Central sites, subbituminous coal of the Hat Creek Coalfield around Hat Creek hosts an entombment biota, the Hat Creek amber, which preserves highlands faunal elements that are not found in the compression biotas. [9] [4] Initial discussion of the amber presented by George Poinar, Jr. et al. (1999) suggested the Hat Creek amber producing tree was likely to be an araucarian tree in the genus Agathis , based on unreported magnetic resonance spectroscopic analysis and earlier reports of the genus in Mesozoic Canada. [12] A purported occurrence of Araucaria at the McAbee site was used as additional support for the ambers origin. [13] The Agathis origin for Canadian Mesozoic amber was later called into question by Ryan McKellar and Alexander Wolfe (2010) based on a lack of any araucarian macrofossil history in the northern hemisphere [12] the McAbee fossils having been already reidentifed as from the cupressaceous Cunninghamia . [13] Based on Fourier-transform infrared spectroscopic analysis and associated amber inclusion fossils, they suggested the Mesozoic ambers of Canada to be from the extinct cupressaceous genus Parataxodium . [12] The origin of the Hat Creek ambers was further noted as likely from a cupressaceous source by Grimaldi et al. (2018) who call out a primary floral component of the host coal being Metasequoia and that the coeval Puget Group Tiger Mountain amber of Washington state is also of Metasequoia origins. They hypothesize that the major amber producing plant of the Paleocene Pacific Northwest forests as Metasequoia, but note that further investigation of Chickaloon, Hat Creek, Coalmont, and Tiger Mountain ambers would be needed. [10]
Mollusks are a rare component of the highlands, usually being mentioned only in passing, such as by Mark Wilson (1977, 1978), [14] [15] and with fossils being reported from three sites only. A series of species were described from several Allenby Formation sites around Princeton by Russell (1957), who documented 4 gastropod species, and tentatively identified to genus another gastropod and a bivalve. [16] Additional unidentified small bivalve fossils were mentioned from the Pleasant Valley site by Wilson (1977) and the Quilchena site by Wilson (1987), [17] while unidentified gastropods were briefly mentioned by Kathleen Pigg et al. (2018). [18]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| A hydrobiid mud snail | ||||
| A lymnaeine pond snail | ||||
Physidae |
| An aplexine bladder snail | |||
| A physine bladder snail | ||||
Planorbidae |
| An ancylinine ramshorn snail | |||
Gyraulus ? | Indeterminate [16] |
| A possible planorbinine ramshorn snail | ||
Indeterminate [16] |
| A possible sphaeriine fingernail clam | |||
Unidentified | Unidentified |
| Unidentified freshwater bivalves. | ||
Unidentified | Unidentified | Unidentified [18] |
| Unidentified freshwater gastropods. | |
In the initial description of Hat Creek Amber, Poinar et al. make note of nematode specimens found in the deposit, with a brief commentary regarding them as the oldest terrestrial free-living nematode fossils to have been found up to that point, but did not give any specific taxonomic identification beyond that. [9]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified | Unidentified [9] |
| Unidentified terrestrial specimens in amber | |
A single arachnid has been described fully from the Okanagan highlands, the Nursery web spider Palaeoperenethis thaleri , known from an adult male. This spider was likely aquatic as are the other members of the family, and based on morphological similarities, it was possibly closer in relation to African and Asian species in the Perenethis genus group then to the only modern genus in British Columbia Dolomedes . [19] Another spider specimen, University of Alberta 5007 was noted by Wilson (1977) from the Kamloops area, while various spiders have been attributed to the McAbee fossil beds. [20] Undescribed male and female orb-web spiders were figured by Wehr (1998) from the Princeton area. [21] Unspecified spider compression fossils were mentioned as occurring in passing by David Greenwood et al. (2005) while discussing the increasing taxonomic richness of the highlands, but without specific site information. [22] Additionally, undiscussed amber fossils were mentioned by Poinar et al. (1999) in their initial report of Hat Creek amber inclusions. [9] Other arachnid evidence has been recovered in the form of fossil hymenopterans placed in families known predate or parasitize spiders. A diverse undescribed fauna of the "parasitoid" wasp family Ichneumonidae is known, some species of which are known to parasitize eggs or adult spiders. Another family, Sphecidae, which is a documented opportunistic predator of spiders and certain insets is known from a few isolated fossils at McAbee and Republic. Lastly the vespoid family Pompilidae has been found at both McAbee and Republic. This family, known as spider wasps, are behaviorally specialized as predators of spiders and a few other arachnids, provisioning newly laid eggs with a single spider as a larder to feed on while developing. [4] Galling preserved on Acer species leaf fossils has been attributed to mites in the family Eriophyidae. [23]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified [21] |
| An orb-weaver spider | ||
| |||||
Unidentified | Unidentified [23] |
| Trace fossils | ||
Unidentified | Unidentified |
| Spider Compression fossils from Kamloops area locations | ||
Unidentified [24] |
| Possible Araneidae? or Tetragnathidae? fossils | |||
Unidentified [22] |
| Spider compression fossils from unspecified highlands locations | |||
Unidentified [9] |
| Spider specimens in amber | |||
The earliest report of Crayfish from the highlands was by Wesley Wehr and Lisa Barksdale (1995). In a short Washington Geology article they reported the first identified occurrence of feathers from the Klondike Mountain Formation and crayfish from both there and the McAbee site. At that time, the moulted carapace section from Republic was not identified further than as a freshwater crayfish. The McAbee specimen was tentatively identified, from photograph, as being a possible Procambarus species fossil by malacologist Rodney M. Feldmann. [25] Subsequently an additional series of over ten fossils were recovered from McAbee and described in 2011 as Aenigmastacus crandalli by Feldmann, Carrie Schweitzer, and John Leahy. A. crandalli was placed in the southern hemisphere superfamily Parastacoidea based on several morphological characters, and they noted this species to be the only northern hemisphere member of the superfamily. [26]
At the Quilchena site, brief mention was reported in 2016 of ostracod fossils, though no further discussion or description has happened. [27]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| A parastacid crayfish. | ||||
unidentified | Unidentified | unidentified [25] |
| An unidentified crayfish | |
unidentified | Unidentified |
| Unidentified ostracod shells | ||
In the initial description of Hat Creek Amber, Poinar et al. make note of a single adult Corydiinae cockroach specimen found in the amber, with a brief commentary on the modern tropical-subtropical distribution of that subfamily and a lack of any native cockroach species in western Canada, but did not give any specific taxonomic identification for the specimen beyond that. [9]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed |
| Undescribed Diplopterine cockroaches. | |||
Undescribed | Undescribed [29] |
| A blattoidean cockroach | ||
Unidentified | Unidentified [9] |
| An undescribed corydiine cockroach | ||
Unidentified | Unidentified [20] |
| Harvester termites | ||
Undescribed |
| ||||
undescribed | Undescribed | Undescribed [29] |
| Undescribed termites of uncertain affiliation | |
The order Coleoptera is divided into four major lineages, Adephaga, Archostemata, Myxophaga, and Polyphaga, with the last group being the most species diverse of the four. Hat Creek amber has provided one fully described beetle species Prionocerites tattriei , [30] which is known from a larval stage specimen first reported by Poinar et al. (1999). [9] The species and genus were the first North American taxon from the family to be described. [30]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Carabidae |
| A sun beetle | |||
Undescribed [27] |
| A sun beetle relative | |||
Undescribed |
| Undescribed ground beetles. | |||
Undescribed | Undescribed [29] |
| |||
Undescribed | Undescribed | Undescribed [33] |
| A caraboid superfamily beetle | |
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed | Undescribed [20] |
| Reticulated beetles | ||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Brentidae |
| ||||
| |||||
Undescribed |
| long-horn beetles | |||
Chrysomelidae |
| ||||
| |||||
Caryobruchus – Speciomerus genus group | Undescribed [37] |
| palm beetles, originally identified as cf. tribe Caryopemina. [27] | ||
Undescribed |
| leaf beetles | |||
Undescribed |
| Undescribed weevils | |||
Undescribed | Undescribed [20] |
| Pintail beetles | ||
| A Prionocerid beetle | ||||
| |||||
Undescribed | Undescribed [20] |
| Undescribed checkered beetle relatives | ||
Undescribed | Undescribed [27] |
| Undescribed pleasing fungus beetle relatives. | ||
Unidentified | Undescribed | Undescribed [33] |
| A cucujiform beetle | |
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Buprestidae | Buprestis |
| |||
| |||||
| |||||
Undescribed | Undescribed [33] |
| A soldier beetle | ||
Elateridae |
| A click beetle | |||
| |||||
undescribed [36] |
| A click beetle. | |||
Undescribed |
| undescribed click beetles | |||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed |
| ||||
Undescribed | Undescribed [20] |
| Bess beetles | ||
| |||||
Undescribed | Undescribed |
| Undescribed scarab superfamily beetles. | ||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Cercyon ? |
| ||||
Undescribed | Undescribed [27] |
| Undescribed Omaliinae rove beetles. | ||
Unidentified | Undescribed | Undescribed [33] |
| A possible staphylinoid beetle | |
Earwig fossils were first noted from republic by paleoentomologist Standley Lewis (1992) in his initial report of the insect diversity at Republic. He noted the fossils to be some of the oldest Eocene demapterans in North America at that time and figured one undescribed specimen consisting of a females abdomen section and cerci. [29] Lewis (1994) tentatively identified the earwigs as members of family Forficulidae based on the shape of the cerci, and illustrated four female fossils, identified as such from the simple straight nature of the cercus. Lewis also suggested two different species were present, based on the differing lengths of the female cerci. [39]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
?Forficulidae | Undescribed | "Forficulid species 1" [39] |
| A forficulid? earwig species with long cerci | |
"Forficulid species 2" [39] |
| A forficulid? earwig species with short cerci | |||
Unidentified [20] |
| A possible forficulid earwig | |||
Undescribed | Undescribed [27] |
| A forficuline earwig of undetermined placement | ||
The most common animal fossils at many of the highlands sites are bibionid march flies, [22] with over twenty species from the genera Penthetria and Plecia described. [40] The modern diversity of the family is greatest in lower latitudes, and Plecia only reaches northward to the warm temperate areas of southeastern North America. [22] In the initial description of Hat Creek Amber, Poinar et al. make note of dipteran inclusions found in the deposit but did not give any specific taxonomic identification of taxa or illustrate any specimen. [9]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed | Undescribed [41] |
| Trace fossils | ||
| A long-legged fly | ||||
Undescribed |
| dagger flies | |||
Pipunculidae |
| ||||
Indeterminate |
| Big headed flies, | |||
Undescribed | Undescribed [33] |
| snipe flies | ||
Unidentified |
| hover flies or, less likely, thick headed flies | |||
The highlands have been noted for the number of Bibionid taxa named in the early work on British Columbian sites. Over 25 unique species have been ascribed to the fossils, with the current count sitting at 22, but doubt has been raised as to the true number of species present and around the generic affinities. The first species was described by Scudder (1879 from the Allenby Formation, while the largest number of species were named by Handlirsch (1910). Following the practice of the time, both Scudder and Handlirsch placed their species in the genus Penthetria . Harrington Molesworth Anthony Rice (1959) reviewed the British Columbian bibionids, notably deeming the majority of species as belonging to Plecia or an undescribed extinct genus and not Penthetria. [40] This placement decision has been questioned however, with Giuseppe Gentilini (1991) asserting the majority of highlands species should be returned to Penthetria. [46] Rice, noted to be a "splitter", [14] also noted the large overlap between the morphology of two species groups and mused that larger collection samples may reveal each group to be single species. He called out in the species discussions the similarities between Plecia avus , P. canadensis , P. dilatata , P. pictipennis , P. pulchra , and P. transitoria , and the similarities between P. curtula , P. nana , P. pulla , and P. reducta . [40]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Bibionidae |
| A possible penthetrian march fly | |||
Penthetria |
| A plecian marchfly | |||
| |||||
Plecia |
| A plecian marchfly | |||
| A plecian marchfly | ||||
| |||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| |||||
| |||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| A plecian marchfly | ||||
| |||||
Undescribed | Undescribed [29] |
| A march fly | ||
Undescribed | Undescribed [45] |
| A bolitophilid fungus gnat | ||
Undescribed | Undescribed [41] |
| Trace fossils | ||
Unidentified | Unidentified [20] |
| long-bodied craneflies | ||
Undescribed | Undescribed [45] |
| A possible keroplatid fungus gnat | ||
Unidentified | Unidentified [20] |
| Limoniid craneflies | ||
Mycetophilidae | Undescribed | Undescribed [45] |
| A gnoristine fungus gnat | |
Undescribed | Undescribed [45] |
| A leiine fungus gnat | ||
Undescribed | Undescribed [45] |
| A mycetophiline fungus gnat | ||
Undescribed | Undescribed [45] |
| A mycomyiine fungus gnat | ||
Undescribed | Undescribed [45] |
| A sciophiline fungus gnat | ||
Undescribed |
| fungus gnats unplaced to subfamily | |||
| |||||
Unidentified |
| dark-winged fungus gnats | |||
Tipulidae |
| A cranefly | |||
Undescribed |
| crane flies | |||
Unidentified | Unidentified [20] |
| winter craneflies | ||
Unidentified | Unidentified | Unidentified [9] |
| Unidentified dipteran specimens in amber | |
Lewis (1992) listed one species of Heptageniidae and three specimens that he did not place to family from Republic. [29] The next year Lewis and Wehr (1993) gave a slightly more detailed description of the specimens again identifying one to Heptageniidae, possibly in the genera Heptagenia or Stenonema . [51] The specimens were later examined by Nina D. Sinitchenkova (1999) who described one as a squaregill mayfly and the oldest member of the genus Neoephemera , confirmed the Heptageniidae identification but that it was unidentifiable to genus. The last specimen she confirmed as an ephemeropteran, but unidentifiable below order level. [52]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Indeterminate |
| A flat headed mayfly | |||
| |||||
Greenwood et al. (2005) briefly discussed the prevalence of Aphid fossils at highlands sites where the taphonomic factors allowed for fine detail preservation such as in the Driftwood shales. [22] Poinar et al. (1999) made note of hemipteran specimens found in Hat Creek Amber but did not give any specific taxonomic identification or illustrate any specimens. [9]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Aphrophoridae | Aphrophora |
| An aphrophorine spittle bug hindwing species. | ||
"Indeterminate" [53] |
| An aphrophorine spittle bug | |||
Undescribed [29] |
| An aphrophorid spittlebug | |||
| |||||
"Indeterminate" [49] |
| An aphrophorine spittle bug | |||
Undescribed [29] |
| An aphrophorid spittlebug | |||
| |||||
Cercopidae | Cercopis |
| |||
| |||||
| |||||
| |||||
| A froghopper | ||||
| |||||
| |||||
Undescribed |
| cercopid froghoppers | |||
Cicadellidae |
| ||||
Undescribed |
| leafhoppers | |||
Undescribed | Undescribed [20] |
| True cicadas | ||
Undescribed | Undescribed [27] |
| A cixiid planthopper | ||
"Indeterminate" [53] |
| An enchophorine lantern bug | |||
Undescribed |
| A ricaniid planthopper | |||
Undescribed | Undescribed | Undescribed [29] |
| A fulgoroidean hopper | |
Incertae sedis |
| A hemipteran [32] of uncertain placement | |||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed | Undescribed [20] |
| Relatives of leaf-footed bugs | ||
Undescribed | Undescribed [27] |
| A cydnid burrowing bug | ||
| A dinidorid shield bug | ||||
Gerridae | Undescribed [20] |
| gerrine water striders | ||
| |||||
† Telmatrechus |
| A gerrine water strider | |||
| A gerrine water strider | ||||
Undescribed |
| A Shield or stink bug | |||
Undescribed | Undescribed [27] |
| Pentatomoid shield bugs of uncertain familial placement | ||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Aphididae | Undescribed |
| Aphids | ||
Undescribed [41] |
| Trace fossils | |||
Unidentified | Unidentified | Unidentified |
| aphidoid specimens | |
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified | Unidentified [9] |
| Hemipterans in amber | |
Archibald, Mathewes, & Aase (2023) reported a Titanomyrma species ant queen from Allenby Formation, 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 suggested 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 . [57]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Cephidae |
| ||||
Undescribed | "Undescribed [4] |
| |||
Cimbicidae [4] |
| ||||
† Leptostigma [58] |
| ||||
| |||||
| |||||
| |||||
| |||||
| |||||
| |||||
Unidentified | Unidentified [58] |
| A cimbicid sawfly of indeterminate subfamily. | ||
| A parasitic wasp | ||||
Siricidae |
| ||||
| |||||
Tenthredinidae |
| ||||
| |||||
Undescribed | Undescribed [4] |
| Sawflys of the tenthredinid subfamily Allantinae | ||
Undescribed [4] |
| Sawflys of the tenthredinid subfamily Blennocampinae | |||
Undescribed [4] |
| Sawflys of the tenthredinid subfamily Nematinae | |||
Undescribed [4] |
| Sawflys of the tenthredinid subfamily Tenthredininae | |||
Undescribed [4] |
| Sawflys of the family Tenthredinidae, unplaced to subfamily | |||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Braconidae | Undescribed [32] |
| A Bracon sensu lato species wasp. | ||
Undescribed | Undescribed [4] |
| braconid parasitic wasps unplaced to subfamily | ||
Undescribed | Undescribed [41] |
| Trace fossils | ||
Cynipidae (?) | Undescribed |
| cynipid Cynipoid gallwasps | ||
Undescribed | Undescribed [4] |
| diapriid diaprioid wasps | ||
Undescribed | Undescribed [4] |
| figitid cynipoid wasps | ||
Undescribed | Undescribed [4] |
| helorid proctotrupoid wasps | ||
Ichneumonidae |
| A xoridine ichneumon parasitic wasp | |||
Undescribed |
| ichneumonid parasitic wasps unplaced to subfamily | |||
Undescribed | Undescribed [4] |
| ceraphronoid Megaspilid parasitic wasps | ||
Undescribed | Undescribed [4] |
| monomachid diaprioid wasps | ||
Undescribed | Undescribed [4] |
| peradeniid proctotrupoid wasps | ||
Undescribed | Undescribed [4] |
| proctotrupid parasitic wasps | ||
Undescribed | Undescribed [4] |
| roproniid (sensu lato) proctotrupoid wasps | ||
incertae sedis [4] | Undescribed | Undescribed |
| Chalcidoid superfamily wasps | |
Undescribed [4] |
| mymarommatoid microhymenopterans | |||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed | Undescribed [4] |
| Chrysidoid wasps of the chrysidid subfamily Chrysidinae | ||
Undescribed |
| pompilid spider wasps | |||
Undescribed |
| Scoliid wasps of the subfamily Archaeoscoliinae | |||
Undescribed | Undescribed [4] |
| trigonalid parasitic wasps | ||
Undescribed | Undescribed [4] |
| Vespid wasps | ||
subfamily | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Dolichoderinae | Undescribed [4] |
| Dolichoderus species ants. [4] Not described to species | ||
Undescribed | Undescribed [4] |
| Dolichoderine ants. [4] Not described to genus/species | ||
Indeterminate [57] |
| A formiciine titan ant. | |||
Formicinae |
| A weaver ant | |||
| A weaver ant | ||||
Indeterminate | indeterminate [62] |
| An weaver ant tribe worker | ||
Undescribed | Undescribed [4] |
| Formicinae subfamily ants. [4] | ||
Myrmeciinae | † Avitomyrmex |
| |||
| |||||
| |||||
| |||||
† Myrmeciites |
| ||||
| |||||
| |||||
| bull dog ants | ||||
| A myrmeciine bulldog ant, first described as a rhopalosomatid wasp. [4] | ||||
† Ypresiomyrma |
| ||||
| |||||
Undescribed | Undescribed [4] |
| Myrmeciinae ants. [4] Not described to species | ||
Undescribed | Undescribed [4] |
| Myrmicine ants of either Leptothorax or Tetramorium [4] Not described to species | ||
Incertae sedis |
| An ant of uncertain subfamily placement [4] | |||
Undescribed |
| Ants of uncertain subfamily placement. [4] | |||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Angarosphecidae | † Eosphecium |
| A spheciform wasp. | ||
Undescribed [4] |
| Spheciform wasps. | |||
Undescribed | Undescribed [4] |
| Spheciform wasps, likely not Eosphecium . | ||
Undescribed | Undescribed [4] |
| Apid bees | ||
Halictidae (?) | Halictus ? |
| A sweat bee of uncertain generic placement | ||
Undescribed | Undescribed [4] |
| sweat bees | ||
Undescribed | Undescribed [4] |
| Megachilid leaf-cutter bee herbivory trace fossils on leaves | ||
Undescribed | Undescribed [4] |
| Sphecid (sensu stricto) wasps | ||
A solitary complete adult female lepidopteran fossil has been recovered, but no full descriptive work has been published on the specimen, aside from a single PhD dissertation. [33] Early examination placed the moth in the family Geometridae, but later work has identified it as the oldest member of the tiger moth subfamily Arctiinae. [67] Two additional isolated wing fossils have been found with one tentatively placed within Noctuidae based on the wing venation and structure, [33] while the second has not been placed beyond order level. [68] Laval mining and hole feeding damage on leaves has been attributed to the families Coleophoridae, Gracillariidae, Heliozelidae, Incurvariidae, and Nepticulidae [41] [69]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| Trace fossils | ||||
Undescribed | Undescribed [67] |
| An arctiine tiger moth | ||
Undescribed |
| Trace fossils | |||
Undescribed |
| Trace fossils | |||
Undescribed [41] |
| Trace fossils | |||
Undescribed [41] |
| Trace fossils | |||
Undescribed [41] |
| Trace fossils | |||
Undescribed | Undescribed [33] |
| A possible owlet moth | ||
Undescribed | Undescribed | Undescribed [68] |
| A lepidopteran forewing | |
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Undescribed | Undescribed [20] |
| hangingfly specimens | ||
†Cimbrophlebiidae | † Cimbrophlebia |
| |||
| |||||
| |||||
| |||||
†Dinopanorpidae | † Dinokanaga |
| |||
| |||||
| |||||
| |||||
| |||||
| |||||
Eomeropidae | † Eomerope |
| |||
| |||||
| |||||
†Eorpidae | † Eorpa |
| |||
| |||||
| |||||
† Holcorpa |
| ||||
Undescribed | Undescribed [74] |
| Undescribed common scorpionflies | ||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| |||||
Chrysopidae | † Adamsochrysa |
| |||
| |||||
† Archaeochrysa |
| ||||
| |||||
| |||||
| |||||
| |||||
| |||||
| A corydasialid lacewing | ||||
Hemerobiidae |
| A hemerobiid lacewing | |||
| |||||
Undescribed | Undescribed [20] |
| Brown lacewing specimens | ||
Ithonidae |
| An Ithonid group moth lacewing | |||
† Palaeopsychops |
| A polystechotid group moth lacewing | |||
| A polystechotid group moth lacewing | ||||
| A polystechotid group moth lacewing | ||||
| A polystechotid group moth lacewing | ||||
| A polystechotid group moth lacewing | ||||
† Polystoechotites |
| A polystechotid group moth lacewing | |||
| A polystechotid group moth lacewing | ||||
| A polystechotid group moth lacewing | ||||
| A Polystoechotid-group moth lacewing [86] | ||||
Undescribed | Undescribed [20] |
| Polystoechotid-group moth lacewings | ||
Nymphidae |
| A split-footed lacewing, possibly sister species to † Nymphes georgei | |||
| A split-footed lacewing | ||||
Osmylidae | † Osmylidia |
| |||
| |||||
Indeterminate [90] |
| A protosmyline osmylid lacewing, | |||
Undescribed | Undescribed [20] |
| osmylid lacewing specimens | ||
| A possible psychopsid lacewing | ||||
Undescribed | Undescribed | Undescribed [20] |
| Members of an undescribed neuropteran family | |
Trace fossil evidence of damselflies has been recorded from oviposition scars on various leaves from the Klondike Mountain Formation that have been placed in the ichnogenus Paleoovoidus . Lewis and Carrol (1991) originally identified the damage on an Alnus parvifolia leaf as caused by leaf beetles of the genus Altica . This was later questioned by Conrad Labandeira who noted the scar patterns did not match modern Altica egg laying behaviour.
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Aeshnidae |
| ||||
† Eoshna |
| ||||
| |||||
† Ypshna |
| ||||
| |||||
†Dysagrionidae |
| ||||
† Dysagrionites |
| A probable dysagrionine cephalozygopteran odonate | |||
| A probable dysagrionine cephalozygopteran odonate | ||||
† Okanagrion |
| ||||
| |||||
| |||||
| |||||
| |||||
| |||||
| |||||
| |||||
† Okanopteryx |
| ||||
| |||||
| |||||
| |||||
| |||||
† Allenbya |
| A possible Dysagrionidae odonate. | |||
| A gossamerwing damselfly. | ||||
| |||||
| A possible cephalozygopteran odonate | ||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified [20] |
| Catanopine short-horned grasshopper specimens | ||
Unidentified | Unidentified [20] |
| Possible leaf-rolling cricket specimens | ||
| |||||
†Palaeorehniidae |
| ||||
| A palaeorehniid ensiferan. | ||||
Unidentified | Unidentified [20] |
| grig specimens | ||
Unidentified | Unidentified [20] |
| katydid specimens | ||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| |||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified | Unidentified [20] |
| stonefly specimens | |
The only reported Psocodea fossils from the highlands are known from Hat Creek amber. They were mentioned, as "Psocoptera", in passing by Poinar et al. (1999) who did not give any finer taxonomic detail or illustrate any specimens. [9]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified | Unidentified [9] |
| specimens in amber | |
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| |||||
Raphidiidae |
| ||||
† Megaraphidia |
| ||||
| |||||
| |||||
| |||||
Poinar et al. (1999) illustrated a Thrips specimen in Hat Creek amber and noted the presence of the order in the fossils they examined, however they did not provide any finer taxonomic details on the affinities of the fossils. [9]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | Unidentified | Unidentified [9] |
| specimens in amber | |
Trichopterans are known mainly from laraval cases and occasional isolated wings. [27]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Unidentified | unidentified [29] |
| northern caddisflies | ||
Unidentified |
| giant caddisflies | |||
Unidentified | Unidentified |
| Isolated wings and larval cases | ||
The first fish to be described from the Okanagan Highlands were recovered from Allenby Formation shales and subsequently studied by Edward Drinker Cope who named Amyzon brevipinne in 1894. The next descriptive work for a fish came in 1916 with the naming of "Lucious" rosei by Louis Hussakof from Tranquille Formation fossils collected at "Red point" on Kamloops Lake in 1914. [100] "Lucious" rosei was redescribed in 1966 by Ted Cavander, who moved the species to a new genus Eohiodon placed into the mooneye family Hiodontidae. The largest body of work for fish of the Highlands was by Mark Wilson (1977) who published a monograph detailing the Canadian highlands formations fish fauna, naming four new species in three new genera, plus redescribing both "Amyzon" brevipinne and "Eohiodon" rosei. The monograph added the families Salmonidae with Eosalmo driftwoodensis , Libotoniidae with Libotonius blakeburnensis , and Moronidae with Priscacara aquilonia . [24] A year later the first species from the Republic area, "Eohiodon" woodruffi was described by Wilson, [101] and the second Republic species Libotonius pearsoni followed in 1979. [102] in 1982 the final new fish species named from the highlands, Amia hesperia , was described, being initially placed by Wilson in the modern bowfin genus Amia . [103] This placement was later questioned by Lance Grande and William Bemis (1998), who noted that due to preservational orientation of the A. hesperia holotype, generic placement of the species was problematic. Phylogenetic analysis of Amiidae fossils by Grande and Bemis found the fossil as a member of the amiinae subfamily, but with key mouth anatomy missing, were unable to determine if Amia or the extinct genus Cyclurus was correct. [104] In 2021 fossils of "Amyzon" brevipinne were redescribed by Juan Liu based on the holotype and additional fossils from the Allenby Formation, and based on the anatomical differences between the species and the type species of Amyzon mentale determined that the Princeton fossils were part of a different genus. As such Liu moved the species to the new genus Wilsonium . [105]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Amiidae | Amia ? |
| |||
† Amia? hesperia ? [28] [103] |
| ||||
Catostomidae | † Amyzon |
| A sucker | ||
| A sucker | ||||
† Wilsonium |
| A catostomid sucker, | |||
| A catostomid sucker, | ||||
Hiodontidae | Hiodon |
| A mooneye, first described as Lucious rosei (1916), | ||
| A mooneye, first described as Eohiodon woodruffi. [101] | ||||
Unidentified [28] |
| A mooneye jaw. | |||
†Libotoniidae | † Libotonius |
| A sand roller relative. | ||
| A sand roller relative. | ||||
| |||||
Salmonidae | † Eosalmo |
| A basal Salmon | ||
| A basal Salmon | ||||
The only reptile fossils known from the Okanagan highlands come from the Allenby Formation. A soft-shelled turtle is known from the "Ashnola shales" unit and unidentified turtle bone are known from the interbedded Princeton Chert. The soft shelled turtle was first discovered by James Basinger from dark shale layers above the chert and reported by Wilson (1982). [103] The unidentified turtle bones were found preserved within the chert layers and first reported by Stockey and Pigg (1994). [110] In his 1995 Masters thesis, G. Guthrie listed an isolated tooth from the Quilchena site as from a crocodile, which would have been the only instance of a crocodylian in the highlands. [28] The taxonomic affinity was later revised after further examination and Mathewes et al. (2016) listed the specimen as an unidentified fish tooth. [111]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Cf. Apalone or Aspideretes |
| A soft shelled turtle | |||
Undescribed | Undescribed | undescribed [110] |
| A turtle, | |
A small avifauna is known from the Okanagan Highlands, but due to the incomplete nature of the fossils, placement of studied specimens has been tentative at best. [113] Gerald Mayr et al. (2019) published an initial overview of the fossils with descriptions and commentary of the material, noting the taxa identified were all previously unknown to Northwestern North American Eocene sites. Despite the tentative nature of the fossil identifications, the Highlands sites are the richest Paleogene avifauna described from Canada. Mayr et al. (2019) posited that the fossils likely represent the more common species in the avifauna of the Highlands, but at the same time, include taxa that are considered rare or absent in the most studied avifaunas from the same time frame. [113] Additional evidence of birds at some sites consists of preserved egested bird pellets, which are composed of randomly grouped fish bone clumps, occasionally including multiple fish or insects. [28]
Isolated feathers are also known from several of the sites and have not described in detail. [113]
Order/Clade | Family | Material | Sites | Notes | Images |
---|---|---|---|---|---|
indeterminate | partial skeleton |
| a large possible Coliiform, | ||
indeterminate | left wing and partial right wing, with feathers |
| a possible gaviiform, | ||
articulated postcranial skeleton |
| A possible songziid bird, | |||
complete, but poorly preserved, skeleton |
| a possible zygodactylid, | |||
indeterminate [113] | indeterminate | partial skeletons |
| partial skeletons missing details for identification. | |
indeterminate | feathers |
| isolated feathers | ||
Eocene mammals are exclusively known from sites in, or possibly in, the Okanagan Highlands. The earliest reported mammals were of teeth from the Princeton area in 1935, with one of the fossils subsequently being "lost". More recent work in 2014 and 2017 on fossils from Driftwood and Princeton have expanded the mammal families to three, possibly four, and an undescribed Quilchena fossil being identified as a "lipotyphla". [114] [5] The record of Brontotheriidae is uncertain due to the split opinion regarding inclusion of the Quesnel area sediments as part of the Highlands. [5] [4] [2]
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
Erinaceidae |
| A hedgehog and moonrat relative | |||
| An unidentified hedgehog relative, | ||||
Esthonychidae | † Trogosus |
| A tillodont species | ||
| An indeterminate tillodont | ||||
indeterminate [114] |
| ||||
undescribed | undescribed | undescribed [5] |
| A "lipotyphlan" | |
Pellets of fish bone and other animal material which were likely eaten by larger predators and then regurgitated have been reported from the Quilchena and Republic sites. These traces, called regurgitalites, have so far been understudied, with only a few passing mentions in Okanagan highlands literature. [113]
If the Quesnel sites are included as part of the Greater Okanagan Highlands per Archibald et al. (2018) the fauna of the region is expanded by a number of insect taxa, an additional arachnid, and a brontothere.
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| An orb-web spider egg sack. | ||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| |||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| An anthomyiid fly. | ||||
| An anthomyiid fly. | ||||
Undescribed | Undescribed [32] |
| An undescribed robber fly | ||
Undescribed [118] |
| An undescribed long-legged fly. | |||
| |||||
"Lonchaea" |
| A lauxaniid fly. First placed in Lonchaea [118] | |||
| A fungus gnat. | ||||
| |||||
| |||||
| |||||
| |||||
| |||||
| A marsh fly. | ||||
| |||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| A shield bug | ||||
Incertae sedis |
| An aphidomorph of uncertain placement | |||
incertae sedis |
| An aphidoid of uncertain placement | |||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| A myrmicine ant, possibly nomen dubium. [120] | ||||
| An ant of uncertain placement. | ||||
| A dolichoderine ant | ||||
| A formicine ant | ||||
| |||||
| |||||
| |||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
| A hemerobiid lacewing of uncertain subfamily placement | ||||
Family | Genus | species | Sites | Notes | Images |
---|---|---|---|---|---|
indeterminate | indeterminate [122] |
| A Brontotheriina subtribe Brontothere | ||
Driftwood Canyon Provincial Park is a provincial park in British Columbia, Canada. Driftwood Canyon Provincial Park covers 23 hectares of the Bulkley River Valley, on the east side of Driftwood Creek, a tributary of the Bulkley River, 10 km northeast of the town of Smithers. The park is accessible from Driftwood Road from Provincial Highway 16. It was created in 1967 by the donation of the land by the late Gordon Harvey (1913–1976) to protect fossil beds on the east side of Driftwood Creek. The beds were discovered around the beginning of the 20th century. The park lands are part of the asserted traditional territory of the Wet'suwet'en First Nation.
Psychopsidae is a family of winged insects of the order Neuroptera. They are commonly called silky lacewings.
Tilia johnsoni is an extinct species of flowering plant in the family Malvaceae that, as a member of the genus Tilia, is related to modern lindens. The species is known from fossil leaves found in the early Eocene deposits of northern Washington state, United States and a similar aged formation in British Columbia, Canada.
Archiinocellia is an extinct genus of snakefly in the family Raphidiidae known from Eocene fossils found in western North America. The genus contains two species, the older Archiinocellia oligoneura and the younger Archiinocellia protomaculata. The type species is of Ypresian age and from the Horsefly Shales of British Columbia, while the younger species from the Lutetian Green River Formation in Colorado. Archiinocellia protomaculata was first described as Agulla protomaculata, and later moved to Archiinocellia.
Microberotha is an extinct monotypic genus of "beaded lacewing" in the family Berothidae known from a fossil found in North America. When described the genus contained a single Ypresian-age species Microberotha macculloughi.
Ithonidae, commonly called moth lacewings and giant lacewings, is a small family of winged insects of the insect order Neuroptera. The family contains a total of ten living genera, and over a dozen extinct genera described from fossils. The modern Ithonids have a notably disjunct distribution, while the extinct genera had a more global range. The family is considered one of the most primitive living neuropteran families. The family has been expanded twice, first to include the genus Rapisma, formerly placed in the monotypic family Rapismatidae, and then in 2010 to include the genera that had been placed into the family Polystoechotidae. Both Rapismatidae and Polystoechotidae have been shown to nest into Ithonidae sensu lato. The larvae of ithonids are grub-like, subterranean and likely phytophagous.
The McAbee Fossil Beds is a Heritage Site that protects an Eocene Epoch fossil locality east of Cache Creek, British Columbia, Canada, just north of and visible from Provincial Highway 97 / the Trans-Canada Highway. The McAbee Fossil Beds, comprising 548.23 hectares, were officially designated a Provincial Heritage Site under British Columbia's Heritage Conservation Act on July 19, 2012. The site is part of an old lake bed which was deposited about 52 million years ago and is internationally recognised for the diversity of plant, insect, and fish fossils found there. Similar fossil beds in Eocene lake sediments, also known for their well preserved plant, insect and fish fossils, are found at Driftwood Canyon Provincial Park near Smithers in northern British Columbia, on the Horsefly River near Quesnel in central British Columbia, and at Republic in Washington, United States. The Princeton Chert fossil beds in southern British Columbia are also Eocene, but primarily preserve an aquatic plant community. A 2016 review of the early Eocene fossil sites from the interior of British Columbia discusses the history of paleobotanical research at McAbee, the Princeton Chert, Driftwood Canyon, and related Eocene fossil sites such as at Republic.
The Coldwater Beds are a geologic formation of the Okanagan Highlands in British Columbia, Canada. They preserve fossils dating back to the Ypresian stage of the Eocene period, or Wasatchian in the NALMA classification.
Wesmaelius mathewesi is an extinct species of lacewing in the neuropteran family Hemerobiidae known from an Eocene fossil found in North America
Cretomerobius is an extinct genus of lacewings in the neuropteran family Hemerobiidae known from fossils found in Asia. The genus currently contains a single species, the Aptian C. disjunctus.
Cuspilongus is an extinct genus of symphytan wasps in the sawfly family Cephidae and the only genus in the subfamily Cuspilonginae. At the time of its description, the genus comprised a single species, Cuspilongus cachecreekensis. A second species, Cuspilongus ghilarovi, was transferred from Mesocephus, which it had been ascribed to at the time of description in 1988. The genus is known from fossils found in the Early Cretaceous of Mongolia and Early Eocene of Canada.
Comptonia columbiana is an extinct species of sweet fern in the flowering plant family Myricaceae. The species is known from fossil leaves found in the early Eocene deposits of central to southern British Columbia, Canada, plus northern Washington state, United States, and, tentatively, the late Eocene of Southern Idaho and Earliest Oligocene of Oregon, United States.
Fagus langevinii is an extinct species of beech in the family Fagaceae. The species is known from fossil fruits, nuts, pollen, and leaves found in the early Eocene deposits of South central British Columbia, and northern Washington state, United States.
Polystoechotites is an extinct parataxon of lacewings in the moth lacewing family Ithonidae. The taxon is a collective group for fossil polystechotid giant lacewing species whose genus affiliation is uncertain, but which are distinct enough to identify as segregate species. Polystoechotites species are known from Eocene fossils found in North America and is composed of four named species Polystoechotites barksdalae, Polystoechotites falcatus, Polystoechotites lewisi, and Polystoechotites piperatus, plus two unnamed species. Three of the described species are known from fossils recovered from the Eocene Okanagan Highlands of Washington State, while the fourth is from Colorado.
Republicopteron is an extinct orthopteran genus in the katydid-like family Palaeorehniidae with a single described species, Republicopteron douseae.
The Paleobiota of the Klondike Mountain Formation comprises a diverse suite of Early Eocene plants and animals recovered in North Central Washington State from the Klondike Mountain Formation. The formation outcrops in locations across the north western area of Ferry County, with major sites in Republic, north west of Curlew Lake, and on the Toroda Creek area. The formation is the southern most of the Eocene Okanagan Highlands, sharing much of the paleoflora and paleofauna with site across Central and southern British Columbia.
Okanagrion is an extinct odonate genus in the damselfly-like family Dysagrionidae. The genus was first described in 2021 with a series of eight species included from early Eocene Okanagan Highlands sites in western North America. The genus is known from the Late Ypresian sediments exposed in northeast central Washington at Republic where five species are present, and from the coeval McAbee Fossil Beds near Cache Creek in Central British Columbia, where four species are present. The species richness is attributed to high latitude high alpha diversity resulting from climatic equitability during the Early Eocene in combination with resultant beta diversity between sites due to impassible topographical barriers.
Allenbya is an extinct odonate genus possibly in the damselfly-like family Dysagrionidae with the single included species Allenbya holmesae. The genus was first described in 2022 from an Early Eocene Okanagan Highlands site in western North America. The species is known from the late Ypresian sediments exposed around Princeton in Central British Columbia.
Republica is an extinct zygopteran genus in the damselfly family Euphaeidae with a single described species, Republica weatbrooki. The species is solely known from the Early Eocene sediments exposed in the northeast of the U.S. state of Washington.
Libotonius is an extinct genus of percopsiform fish which lived during the early Eocene epoch and contains two species, the type species Libotonius blakeburnensis plus Libotonius pearsoni. Libotonius has been variously treated as part of the expanded Percopsidae family, or formerly as a member of the monotypic family Libotoniidae.