Fagopsis is an extinct genus of beech relative in the family Fagaceae with two accepted species – Fagopsis longifolia and Fagopsis undulata. It has been found in fossil strata ranging in age between the Early Eocene to the Late Eocene or Early Oligocene in British Columbia, Colorado, Montana, and Washington. Several other species were formerly placed in the genus, but later removed because of insufficient associated fossils.
The Florissant Formation is composed of successive lake deposits resulting from a volcanic debris flow damming a valley. When Fagopsis longifolia was originally described, the Florissant Formation was considered to be Miocene in age, based on the flora and fauna preserved. Successive research and fossil descriptions moved the age older and by 1985 the formation had been reassigned to an Oligocene age. Further refinement of the formation's age using radiometric dating of sanidine has resulted in an age of placing the formation in the Priabonian stage of the Late Eocene.
The type locality of Fagopsis unduata was given by paleobotanist Frank Hall Knowlton as on the bank of the Yellowstone River between Elk Creek and Hellroaring Creek. When collected in 1899 the area was assumed to belong to the Fort Union group and Paleocene in age. Following extensive geological mapping and field work the regional geology was reclassified by Harry W. Smedes and Harold J. Prostka in 1972 who formally subdivided the Absaroka Volcanic Supergroup into a number for groups and formations. The Yellowstone river location was one of a number of fossil bearing sites that were included in the nearly named Sepulcher Formation of the Washburn Group. Sanidine crystals from the Lost Creek Tuff Member provided potassium–argon radiometric dating ages of around 49.2±1.5 mya. This places the type locality as equal to the younger sites in the Okanagan Highlands.
Fagopsis is known from a series of six geologic formations in the Eocene Okanagan Highlands, with four occurrences of F. undulata and two defined as Fagopsis only. Leaves and fruits of F. undulata are known from the Klondike Mountain Formation sites around Ferry County, Washington, and the "Horsefly shales" near Horsefly, British Columbia. Isolated leaves, without fruits, are reported from the Allenby Formation near Princeton and the Coldwater Beds near Stump Lake, British Columbia. The two additional British Columbian Sites with unidentified Fagopsis are the Tranquille Formation near Cache Creek and the "Driftwood shales" near Smithers.
Early estimates of the highlands sites ranged from Miocene to Eocene in age. The age of the Klondike Mountain Formation was debated for many years, with plant fossils suggesting a Late Oligocene or Early Miocene age, and the first descriptions of species from the area included them in the Middle Miocene Latah Formation. By the early 1960s the Klondike Mountain formation was thought to be late Oligocene in age. Potassium–argon radiometric dating of samples taken near the Tom Thumb mine in 1966 resulted in a tentative age. Further refinement of sample dating has yielded an approximately Early Eocene, Ypresian age, being radiometrically dated as . A 2003 report using dating of detrital zircon crystals with the tuffs of the Klondike Mountain Formation had been dated to , the youngest of the Okanagan Highlands sites, A 2021 radiometric analysis report revised the possible oldest age to around based on isotopic data from zircon crystals.
As with other Okanagan sites, the age of the Allenby Formation was debated for many years, with fish and insect fossils hinting at an Eocene age, while mammal and plant fossils suggested a Late Oligocene or Early Miocene age. The lake sediments at Princeton were radiometrically dated using the K–Ar method in the 1960s based on ash samples exposed in the lake bed. These samples yielded an age of ~; however, dating published in 2005 provided a 40Ar–39Ar radiometric date placing some Princeton sites at . Dating obtained in the 2021 radiometric analysis paper consistently reaffirmed ages in the Late Ypresian, with oldest likely ages between .
While the historic Tranquille Formation site along the Tranquille River has not been reassessed in modern works, the related McAbee Fossil Beds west of Cache Creek in central British Columbia have been. The lake sediments at McAbee were first radiometrically dated using the K–Ar method in the 1960s based on ash samples exposed in the lake bed. These samples yielded an age of ~; however, dating published in 2005 provided a 40Ar–39Ar radiometric date placing the McAbee site at . Similar to the Tranquille River sites are the Driftwood Shales in Driftwood Canyon Provincial Park, near Smithers, British Columbia. The same 2005 dating paper established the shales at Driftwood, which had not been formally described, as dating to around in accordance with the other sites of the highlands, a date supported by the presence of the hedgehog-relative Silvacola from the same site.
Fagopsis unduata has additionally been identified from leaves and fruits from small region of Montana. The Ruby Reservoir area in southwestern Montana has been identified as part of the Renova Formation which is comprised of varying fissure fill deposits, riverine systems, and small shallow lakes which were all active during the transitional period across the Grande Coupure of the Latest Eocene to Youngest Oligocene.
In 1899 Knowlton published his work on the fossils of the "Green River Series" in Yellowstone National Park and some surrounding localities. Based on a small series of partial leaves collected from along the Yellowstone River he named a new Fagus species, Fagus undulata. As with Lesquereux's type description, Knowlton did not designate a type series, and it so specimens were selected by Peale, who chose USNM 5126, USNM 5136, and USNM 5185 as lectotypes. This placement went unchallenged until 1987 when new fossils from north central Washington were described by Jack Wolfe and Wesley Wehr. Based on similarities between the new fossils from around Republic, Washington, they moved Fagus undulata to Hollicks genus Fagopsis as Fagopsis undulata.
During the period between 1890 and 1910 a series of fossils were described from sites in central to southern central British Columbia by John Dawson and David P. Penhallow. Starting in 1890, Dawson identified a partial leaf from Stump Lake as Carpinus grandis, a European fossil species from the Croatian Miocene. Then in 1902, Penhallow noted a number of fragmentary leaves he placed into Planera longifolia recognizing the similarities of the leaves to those of Florissant. The largest increase in distribution came with Penhallows 1908 overview of fossils collected since the 1870s and detailing collections made under the oversight of Canadian chief geologist Laurance Lambe in 1906. This paper saw the expansion of "C. grandis" leaves to the Princeton area at Tulameen and Similkameen River sites, along with sites on the Tranquille River, and at Quilchena. For "P. longifolia", he mentions occurrences on the North Fork Similkameen River, Tulameen River, and Tranquille Rivers in addition to Horsefly.
In their 1987 redescription of Fagopsis undulata, Wolfe and Wehr included the Carpinus grandis fossils, as circumscribed by Dawson, within their expanded Fagopsis species. Thus the occurrences in the Coldwater Beds, Allenby Formation, Tranquille Formation and Horsefly Shales were identified to F. undulata. In 2023, Pigg, Manchester, and DeVore reviewed the Horsefly flora for the first time in a century. They specifically noted the fossils that had been identified as P. longifolia were actually F. undulata confirming Wolfe and Wehrs assessment. The only Okanagan Highlands specimens that have not been addressed to Fagopsis species are the Tranquille Formation fossils, which Richard Dillhoff, Estella Leopold, and Steven Manchesters 2005 overview of the McAbee Flora only listed to genus. In the same paper they noted the occurrence of Fagopsis sp. fossils at Driftwood Canyon.
Placement within Fagaceae has been considered unclear, with work the work of Manchester and Crane (1983) suggesting placement close to some Quercus species. Later work by Bouchal et al (2015) examining F. longifolia pollen showed instead a plausible relationship to some extinct and living members of the genus Castanopsis.
Three additional species were historically included in Fagopsis, but have subsequently been moved. Fagopsis groenlandicum, Fagopsis nipponica and Fagopsis rarytkinensis are known from isolated leaf fossils found in East Asia, North America, Greenland, and Europe. Unlike the two accepted species however, the three transferred species have not been found in association with the distinctive wedge shaped fruits of true Fagopsis. As such Manchester (1999) moved the three to a new morphogenus Fagopsiphyllum as Fagopsiphyllum groenlandicum, Fagopsiphyllum nipponica and Fagopsiphyllum rarytkinensis. Manchester specified the new genus was for isolate leaf species which resembled Fagopsis but had not been found with the fruits.
The leaves are up to long and wide, resulting in length to width ratios of 1 to 2 and 1 to 3. They have a petiole that is long and wide. The teeth are non-glandular and simple, with a supporting vein terminating in the tooth tip. The secondary veins are sub-opposite to alternate in position on the primary vein.
The male pollen cones are spherical in shape, ranging between in diameter, and comprised of numerous flowering heads. The cones develop on peduncles which reach up to in length by wide. Each flower has a filament and two basifixed anthers, each with two pollen sacks. On specimens with the cones still attached to branches, the cones are produced on small side branches of the main stem, and no female cones are present.
A detailed examination of pollen extracted from fossils was published by Johannes Bouchal et al in 2014. The overall pollen grain architecture is closer to subfamily Castaneoideae genera and not Quercus or Fagus. The pollen grains are produced as monads, with each grain separate from the other, rather than being triads or tetrads with multiple grains fused together. The grains range between spheroids to prolate, lemon-shaped, in outline. Pollen grains in the cones still were measured to have polar diameters between 22 and 27 µm, and an equatorial diameter of 19–21 µm. Loose pollen gains from sediment samples are slightly larger, with diameters of 22–28 µm polar and 19–26 µm equatorial. The grains have a threefold symmetry, being tricolporate and showing three germination furrows which range between 18 and 22 µm in length. The surface has microtexturing expressed as minute ridged textures, microrugulae, which combine into larger ridges which form a vermiculate "can of worms" sculpturing.
Unlike the male cones, female cones are ellipsoidal during early growth and pollination stages, with sizes averaging long and wide. The main body is surrounded by elongated filaments that Manchester and Crane deemed styles. The styles are grouped in threes with the tips curving in a slight hook and extend above the surface of the cone between .
After pollination the cones develop into fruiting cones, with an increased mature length between and width between . The fruiting head is comprised of approximately 40 "fruit wedges", possibly cupules, which are arranged in a helical pattern on the central axis. The basal and apical fruits appear to have been more firmly attached to the central axis and were frequently not shed when the central fruits were. After shedding fruits, the central axis shows scarring from each fruit shed. The scars are grouped in threes and have an encircling affixed bract.
The cupules are a wedge or cone shaped, having a base which flares over length to a wide heads. The head has up to nine minute teeth ringing the upper edge. Each internal side of the fruits appear to have been covered by mats of fine 50+ µm long hairs. The fruits are often divided into two to three sections vial longitudinal creases on the fruit sides. At the base of each fruit section are small fruits with ovoid outlines. The long axis are and the short sides are .
A full description of the female cones found associated with the F. undulata leaves at Resner Canyon and Graphite Creek was not provided, but they were noted to be smaller overall then the female cones of F. longifolia.
The Allenby and Klondike Mountain Formations represent a series of long upland lake systems that were surrounded by a warm temperate ecosystem with nearby volcanism dating from during and just after the early Eocene climatic optimum. The Okanagan Highlands likely had a Mesic habitat Microthermal to mesothermal climate, in which winter temperatures rarely dropped low enough for snow, and which were seasonably equitable. The paleoforest surrounding the lakes have been described as precursors to the modern temperate broadleaf and mixed forests of Eastern North America and Eastern Asia. Based on the fossil biotas the lakes were higher and cooler then the coeval coastal forests preserved in the Puget Group and Chuckanut Formation of Western Washington, which are described as Tropical forest ecosystems. Estimates of the elevation range between higher than the coastal forests. This is consistent with the paleoelevation estimates for the lake systems, which range between , which is similar to the modern elevation , but higher.
Estimates of the Climate have been derived from climate leaf analysis multivariate program (CLAMP) analysis and leaf margin analysis (LMA) of the Republic paleoflora. The CLAMP results after multiple linear regressions gave a mean annual temperature of approximately , with the LMA giving . A bioclimatic-based estimate based on modern relatives of the taxa found at Republic suggested mean annual temperatures around . This is lower than the mean annual temperature estimates given for the coastal Puget Group, which is estimated to have been between . The bioclimatic analysis for Republic suggests a mean annual precipitation amount of .
The Florissant paleoforest surrounding the lake has been described as similar to modern southeastern North America, with a number of taxa represented that are now found in the subtropics to tropics and confined to the old world. MacGinitie (1953) suggested a warm temperate climate based on the modern biogeographic relatives of the biota found in the formation. Modern estimates of the elevation range between , notably higher than the original estimates by MacGinitie of . Estimates of the Climate for the Florissant Formation have been derived from CLAMP analysis and modern forest equivalencies of the paleoflora. The results of the various methods have given a mean annual temperature rage between approximately , while the bioclimatic analysis for suggests mean annual precipitation amounts of .
The Renova Formation preserves a mosaic landscape with streams and small lakes located at high to middle altitudes and fairly climatologically buffered from the Grande Coupure changes across the Eocene-Oligocene boundary. The continued Laramide orogeny uplift of the Rocky Mountain belts to the west likely provided some stabilization of the seasonal temperatures and precipitation rates compared to sites of similar age to the north and south. The mountain lakes were likely surrounded by temperate forests.
Description
F. longifolia
F. undulata
Paleoecology
Paleoenvironment
External links
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