We describe a partial skeleton of a large-sized owl from Wasatchian strata of the Willwood Formation (Wyoming, U.S.A.). The holotype of Primoptynx poliotauros, gen. et sp. nov., includes all major postcranial bones and is one of the most substantial Paleogene records of the Strigiformes. The fossil shows that owls exhibited a considerable morphological diversity in the early Eocene of North America and occupied disparate ecological niches. As in the protostrigid taxon Minerva from the late early to early middle Eocene of North America, but unlike in extant owls, the ungual phalanges of the hallux and the second toe of the new species are distinctly larger than those of the other toes. Primoptynx poliotauros gen. et sp. nov., however, does not exhibit the derived tibiotarsus morphology of the Protostrigidae. Even though the new species may well be a stem group representative of protostrigid owls, current data do not allow an unambiguous phylogenetic placement. Concerning the size of the ungual phalanges, the feet of P. poliotauros correspond to those of extant hawks and allies (Accipitridae). We therefore hypothesize that it used its feet to dispatch prey items in a hawk-like manner, whereas extant owls kill prey with their beak. Primoptynx and protostrigid owls were possibly specialized in foraging on prey items that required an accipitrid-like killing strategy, such as larger-sized or more defensive mammals. The extinction of these peculiar owls may have been related to the radiation of accipitrid diurnal birds of prey, which appear to have diversified in the late Eocene and early Oligocene.
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RBINS Staff Publications 2020
In 1880, the early Eocene fluvial deposits of the Erquelinnes sand quarry in the southern part of the Mons basin in Belgium yielded their first mammal fossil, a well preserved jaw of a primitive perissodactyl. By 1927, about 40 mammal specimens had been recovered from Erquelinnes and were attributed to Adapisorex, ‘Protomomys’, Paramys, Plesiadapis, Arctocyonides, Hyracotherium, Coryphodon and ‘Oxyaena or Miacidae’. By that time however, the Erquelinnes fauna had already been eclipsed by the contemporaneous Dormaal fauna from northeastern Belgium, which yielded thousands of specimens rather than only a few dozen. Since then, attention for the Erquelinnes fauna has therefore been limited to the passing mentions of referred specimens in the formal descriptions of the new plesiadapiform Platychoerops georgei and of the miacid Gracilocyon solei. Here we present an updated faunal list of the complete Erquelinnes mammal fauna. We show that also hyaenodontids, mesonychids, hyopsodontids, and dichobunid artiodactyls are present in the Erquelinnes fauna, and some of the earlier identifications are corrected or detailed further. This update of the Erquelinnes mammal fauna almost doubles its diversity, and strengthens the correlation with the earliest Eocene (MP7) Dormaal reference fauna. Results from δ13Corg analysis of the mammal-bearing level at Erquelinnes and the strata immediately below it, seem to independently support the faunal correlation. Faunal differences between Erquelinnes and Dormaal are most likely the result of subtle differences in depositional environments and thus in taphonomic bias. Details of the stratigraphic origin of the Erquelinnes perissodactyl specimens however show that these are derived from two distinct stratigraphic levels, which potentially have significantly different age correlations.
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This paper presents a review of records of pollen and botanical macroremains of a selection of food plants from late and post-medieval cesspits (12th century-19th century ad) in the Netherlands and northern Belgium. The presented data demonstrate that several food plants remain largely invisible in the macrobotanical records. These are all plants from which the flowers or flower buds (Borago officinalis, Capparis, Carthamus tinctorius, Crocus sativus, Syzygium aromaticum) or leaves (Anthriscus cerefolium, Spinacia oleracea) are eaten, or that are typical components of honey (Cistus). As a result, little is known about the import or local production and consumption of these food plants in these times. This review now shows that past use of some of these plants is reflected in the pollen assemblages of (post-) medieval cesspits. For the first time, a large archaeobotanical dataset is presented, including pollen, providing information on the past use of these plants between the 12th and 19th century ad in the Netherlands and Belgium.
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RBINS Staff Publications 2019
