Foraging traces associated with the web-footed avian footprint ichnotaxon Presbyornithiformipes feduccii are described. Four new ichnospecies in three new ichnogenera are established to identify and describe the traces that resulted from foraging behaviors. All four ichnotaxa are, in places, overprinted by P. feduccii footprints and occur either laterally to, or sinuously woven between, P. feduccii trackways and therefore were clearly emplaced by the P. feduccii tracemaker.

Erevnoichnus blochi new ichnogenus new ichnospecies is established for a series of pits, joined by a marginal groove, that are associated with web-footed bird trackways. This ichnotaxon is interpreted to record regular probing/gaping as a waterbird swept its head from side to side searching for food. Erevnoichnus strimmena n. igen. new ichnospecies is established for en-echelon, gently arcuate grooves produced through forward probing by a waterbird searching for food. Ravdosichnus guntheri new ichnogenus new ichnospecies is established for simple grooves with u-shaped profiles produced when a waterbird dragged its bill backwards through the sediment. Aptosichnus diatarachi new ichnogenus new ichnospecies is established for a broad, shallow groove/trough characterized by sinuous margins and a complex, irregular fill. It is interpreted to record thorough bill stirring in an area with common prey.

All four ichnotaxa named herein are interpreted to record tactile feeding behavior by a marginal lacustrine waterbird searching for prey. Their association with Presbyornithiformipes feduccii suggests that the purported tracemaker, Presbyornis pervetus, did not forage solely through filter-feeding but was also capable of tactile foraging for larger prey.

UUID: www.zoobank.org/42c5d24b-6e9a-45da-9a48-78f8f040311c

The Lower Ordovician (Floian) Al Rose Formation from the Inyo Mountains, California, is a deeper-water, graptolitic equivalent of the well-known and richly fossiliferous successions described from Utah and Nevada. It is considered to have been originally marginal to the Laurentian paleocontinent. It has yielded a low-diversity trilobite fauna that differs strikingly from contemporary faunas to the east in its abundance of raphiophorid, nileid, olenid, and agnostoid trilobites, resembling that of the Nileid Biofacies known from scattered locations marginal to Laurentia. Two new trilobite species are described: Globampyx sexsegmentatus (Raphiophoridae) and Protopresbynileus divergens (Nileidae). Carolinites genacinaca Ross, 1951 is a link with the Great Basin. Other trilobites include the olenid Cloacaspis cf. C. ceryx anataphra Fortey, 1974, metagnostid Geragnostus cf. G. (Novoagnostus) longicollis Raymond, 1925, and pliomerid Hintzeia sp.

UUID: https://zoobank.org/19a679ce-968d-4ce1-a590-f7f55bf9d62d

In their detailed comments, Das et al. (2023) try to discount our arguments that the strata cropping out at the so-called Jhura pond locality are not Late Jurassic in age but Miocene. We wrote this paper (Fürsich et al., 2023) because of the far-reaching conclusions that have been drawn from the molluscan fauna at that locality, in particular with respect to the evolution of turritellid gastropods and the evolution of drilling predation by naticid gastropods. We still maintain that the beds containing abundant turritellids are not Jurassic but Neogene, most probably Miocene, in age. In no way do we contest the various analyses on the material collected from the outcrop by the authors, but just the erroneous age assignment of the strata. In order to keep this reply short, we support our point by referring to just to two aspects: the position of the outcrop and the composition of the fauna. Rather than refuting each of the other arguments of Das et al. (2023), we think that a joint visit to the locality would be more productive for arriving at a consensus on the origin and age of the fauna of the Jhura pond locality.

The free-living, stalkless comatulids make up the bulk of living crinoid diversity and are the only crinoids remaining in shallow water, but compared to the stalked crinoids their fossil record is fragmentary and understudied, especially outside Europe. We present new Albian fossil comatulids from the Glen Rose Formation, central Texas, and study them using computed tomography, scanning electron microscopy, morphometry, and cladistic analysis of discrete and continuous characters. New material comprises the previously described Decameros wertheimi and Semiometra klari? and the new taxa Semiometra alveoradiata n. sp. and an extremely unusual new form Castaneametra hodgesi n. gen. n. sp. In addition to being exceptionally variable, this species is the largest known comatulid, has the most cirri of any known comatulid, and exhibits unique architectural features and voluminous, through-going coelomic cavities. We reconstruct its paleobiology, infer its phylogenetic affinities, argue for its origin from small Semiometra-like ancestors in a brief Albian North American radiation, and suggest new interpretations of early comatulid phylogeny based on our findings. Adaptive allometry related to respiratory demands, along with an origin by peramorphosis, may explain some features of this odd, short-lived giant.

Soricidae is the most species-rich eulipotyphlan family since the Pliocene. Numerous Late Miocene soricids and plesiosoricids are well known from southern Europe. Localities from central Europe, despite being rare, historically have yielded better preserved material that reveals a great diversity. We here add to this existing record with the description of eight species from MN9- to MN12-aged localities of Slovakia (Paenelimnoecus repenningi, Paenesorex bicuspis, Isterlestes aenigmaticus n. gen. n. sp., Crusafontina endemica, Crusafontina kormosi, Amblycoptus jessiae, Asoriculus gibberodon, Petenyia dubia), alongside one species of Plesiosoricidae (Plesiosorex evolutus). The early occurrence of A. gibberodon and A. jessiae, the occurrence of Paenesorex, and the identification of Isterlestes aenigmaticus n. gen. n. sp., reinforce the hypothesis that the Pannonian region (south-eastern central Europe) was a source area for several soricid taxa (Allosoricinae, Anourosoricini, Soricini) during the Late Miocene.

UUID: https://zoobank.org/4466a6ea-4fc6-4a3b-88f8-dbe020f2292d

Revision of the type species of the Early Ordovician (Tulean, late Tremadocian) bathyurid trilobite Licnocephala Ross, 1951 demonstrates that it has significantly different morphology than that ascribed to it in the earlier literature, which was based largely on species now assigned to a different genus. In addition to the type species, L. bicornuta Ross, 1951, which is fully revised on the basis of new material, four species, all apparently new, have been recovered, two of which, L. ngi n. sp. and L. bradleyi n. sp., are well enough known to formally name. The overall phylogenetic structure of bathyurids is yet to be determined, but several apparent clades can now be recognized and are discussed. Among these is what is termed the “Chapmanopyge group,” including Chapmanopyge Fortey and Bruton, 2013, Punka Fortey, 1979, Uromystrum Whittington, 1953, and Licnocephala. These genera are united in the occurrence of much of the anterior cephalic border on the librigenal anterior projection, with most of the anterior margin of the cranidium representing the suture, the possession of very short (exsag.) strap-like posterior cranidial projections, and extremely narrow visual surfaces. A fifth genus of the group, Ibexocephala n. gen., is represented by two new species, I. lossoae (type species) and I. dekosterae. The taxon features a remarkable cranidial morphology involving a strong deflection of the posteriormost part of the cranidium from the anterior part in sagittal profile.

UUID: http://zoobank.org/ab9a8796-84c7-48b1-b0e5-84a22511a6b4

Jurassic cyrtocrinids from Spain are first documented here as representing relatively diverse assemblages from the western Tethys. The species Ascidicrinus pentagonus, Eugeniacrinites cariophilites, Gammarocrinites compressus, Pilocrinus moussoni, Sclerocrinus cf. S. strambergensis, and Tetracrinus moniliformis are described from Oxfordian marl levels belonging to the Yátova Formation, around Tosos (Zaragoza, NE Spain). Although based on partially disarticulated material, these fossils preserve cups, stem columnals, attachment structures, and brachial plates. Based on the sedimentology and associated invertebrate fauna, cyrtocrinids from this area lived below storm wave action but eventually were affected by storms, as opposed to their modern counterparts that occupy deep water environments. Some specimens preserve traces of interactions with other organisms, such as predation marks or epibiontic colonization during life and post-mortem. Attachment structures suggest cyrtocrinids mostly attached on sponges. We note that diversity of cyrtocrinids changed in step with the abundance of sponge reefs in the Jurassic, suggesting that both groups probably had an important link in that period related with similar ecological requirements.

Fossil egg capsules of chimaeroids (holocephalian fishes), although rare, have been known for more than 150 years (Bessels, 1869; Meunier, 1891a) and have been found in rocks as old as Upper Triassic (Gottfried and Fordyce, 2014). Egg capsules of extant chimaeroids are spindle shaped, with a smooth central body where the embryo develops, an elongate anterior beak through which the hatchling emerges, and an elongate posterior pedicle. The capsules are flanked by a lateral membrane or web on both sides, and the web is reinforced with branching or unbranching rib-like costae that extend laterally from the central body, beak, and pedicle. Specimens are typically about 10–30 cm long. Egg capsules of extant chimaeroids are made of collagen (Hamlett et al., 2005) and as fossils, chimaeroid egg capsules are typically preserved as external casts (Fischer et al., 2014).

Obruchevodid petalodonts are rare small chondrichthyans known from nearly complete to partial skeletons from the Upper Mississippian (Serpukhovian) Bear Gulch Limestone of central Montana and isolated teeth from the Upper Mississippian Bangor Limestone of northern Alabama. New records of obruchevodid petalodonts are presented here from the Middle Mississippian (Viséan) Joppa Member of the Ste. Genevieve Formation at Mammoth Cave National Park, Kentucky. Obruchevodids are here represented by multiple teeth of a new taxon, Clavusodens mcginnisi n. gen. n. sp., and a single tooth referred to ?Netsepoye sp. Clavusodens mcginnisi n. gen. n. sp. is characterized by teeth with pointed mesiodistal and lingual margins and more robust chisel-like cusps on the anterolateral and distolateral teeth. The suggestion that obruchevodid petalodonts evolved to inhabit complex reef-like environments and other nearshore habitats with a feeding ecology analogous to extant triggerfish is explored and discussed.

UUID: http://zoobank.org/0955c37a-c458-4a4d-89c4-01d6915adeca

Intense commercial exploitation of fossils in the famous El Qaid Errami area in the last 20 years has led to the discovery of the interesting Declivolithus Fauna in the Moroccan Anti-Atlas. This unusually large trinucleid trilobite, described originally from the Czech Republic, is the most conspicuous element of an assemblage mainly occurring in the Bofloss locality, a local biofacies development of pelagic mudstones and sandstones cropping out in a structurally isolated place in the Tizi n'Ounfite area. Here we revise this Declivolithus Fauna trilobite assemblage from Morocco, increasing the known trilobite diversity from four to 11 species: Ulugtella? biformis n. sp., Selenopeltis cf. S. vultuosa, Phacopidina quadrata, Eudolatites cf. E. bondoni, Prionocheilus cf. P. verneuili, Nobiliasaphus cf. N. kumatox, Cyclopyge cf. C. rediviva, Symphysops stevaninae, Heterocyclopyge sp., Dionide sp., and Declivolithus alfredi. The new data and the very good preservation of specimens in sandstones, clarify the specific identity of previously reported taxa. Although the stratigraphical correlation of the fossiliferous levels remains problematic, it probably corresponds to the upper part of the Lower Ktaoua Formation or to the lower half of the Upper Tiouririne Formation. Most taxa support previous assignment of the Moroccan assemblage to the late Berounian (ca. early Katian, Ka2), although a middle Berounian (ca. Sa2–Ka1) age cannot be excluded. Most of the identified species are known from the Czech Republic (eight out of 11), showing that the strong faunal link between Morocco and the Czech Republic still existed during the Late Ordovician, being stronger than the link with the coeval Ibero-Armorican domain faunas.

UUID: http://zoobank.org/3e6e55c7-168d-4008-98ba-38a795581ca3

Insights into the paleoneurology and endocranial anatomy of ornithopod dinosaurs come largely from Northern Hemisphere taxa. The recently described non-hadrosaurid iguanodontian Fostoria dhimbangunmal from the Cenomanian of eastern Australia includes a partial skull that offers novel insights into its endocranial anatomy (i.e., the cavity housing the brain). Here, we describe the paleoneurology of F. dhimbangunmal based on a digital cranial endocast obtained from computed tomography. The endocast is mostly complete; however, it is diagenetically dorsoventrally compressed and its ventral limits are not preserved. The endocranial anatomy of F. dhimbangunmal is generally consistent with that of other non-hadrosaurid iguanodontians, including a well-developed olfactory apparatus, suggesting a good sense of smell. In contrast to hadrosaurids and some non-hadrosaurid iguanodontians, F. dhimbangunmal possesses the ancestral flexure condition, in which cranial and pontine flexure angles are subequal. The cerebrum makes up a significant portion of the endocast volume; however, the cerebral hemispheres are not as enlarged or bulbous as seen in hadrosaurids. The forebrain of F. dhimbangunmal did not fill the braincase to the same extent as in hadrosaurids. A distinct vacuity in the supraoccipital of F. dhimbangunmal may represent a new autapomorphy. This study provides the first insights into the neuroanatomy of an Australian iguanodontian dinosaur.

Shape deformation during fossilization can prevent accurate reconstruction of an organism's form during life, hampering areas of paleontology ranging from functional morphology to systematics. Retrodeformation attempts to restore the original shape of deformed fossil specimens and requires an adequate knowledge of the deformation process. Although tectonic processes and retrodeformation are relatively well understood, research on quantifying the effect of compressive deformation on fossil morphology is scant. Here we investigate the factors that can cause changes in the shape of fossil specimens during compressive deformation. Three-dimensional (3D) models of trilobite cranidia/cephala are subjected to simulated deposition and compaction using rigid body simulation and scaling features of the open-source 3D software Blender. The variation in pitch and roll angle is lowest on flat surfaces, intermediate on tilted surfaces, and highest on irregular surfaces. These trends are reflected in the morphological differences captured by principal component scores in geometric morphometric analyses using landmarks. In addition, the different shapes of trilobite cranidia/cephala according to their systematic affinity influence the degree of angular variation, which in turn affects their posture—normal or inverted. Inverted cranidia/cephala show greater morphological variability than those with normal postures.

Harpetid and trinucleid trilobites share a similar and unusual morphology, the most striking feature of which is a wide, flattened cephalic brim with many pits or holes. This similarity was once interpreted as a sign that these two groups of trilobites were closely related, but in recent years it has instead been assumed that the ‘harpiform’ brim arose in both groups independently. However, relatedness and similarity can be difficult to disentangle in fossil taxa without close living relatives, and this assumption about the harpiform brim has never been explicitly tested. Our study re-evaluates the relationship between Harpetida and Trinucleioidea in order to test a longstanding assumption about trilobite relationships and as a case study in evaluating different kinds of morphological similarity in extinct groups. We inferred a new phylogenetic tree using parsimony methods and discrete morphological character data from a broad sampling of harpetids, trinucleids, and their relatives. Despite their gross morphological similarities, we found that harpetids and trinucleids were readily distinguished in our analyses, a result consistent with a hypothesis of multiple origins for the harpiform brim. By mapping brim-related characters across our new phylogeny, we identified a sequence of morphological innovations that arose in parallel in both groups and led ultimately in each case to the evolution of the harpiform brim. These results indicate that harpiform brims are a prime example of parallel evolution—the similar development of a morphological trait in distantly related taxa that nevertheless share a similar original morphology. In addition, our phylogeny supports the idea that trinucleids are specialized, harpiform asaphids, rather than an independent order of trilobites. We also provide new information on the relationships of the putative ‘basal-most’ members of Trinucleioidea, the Liostracinidae, and confirm recent assessments that this family is more distantly related to trinucleids.

Scandentians, commonly known as treeshrews (tree shrews), are the sister group of primates and colugos within the Euarchonta, a clade with an evolutionary history rooted in the Cretaceous (Roberts et al., 2011; Melin et al., 2016). Scandentians are, however, extremely rare in the fossil record (Ni and Qiu, 2012; Li and Ni, 2016) and, other than the Oligocene species Ptilocercus kylin Li and Ni, 2016, their earliest undoubted representatives are not older than 18 Ma (Li and Ni, 2016, and references therein).