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.

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.

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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.

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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.