Ediacaran fossils, obtained in stratigraphic context in 1993, 1995, and 1996, with the assistance of A. Seilacher, IGCP project 320 scientists, and the Geological Survey of Namibia, are described for the first time. Most are from the Kliphoek and Buchholzbrunn members of the Dabis Formation and the Huns and Spitskop members of the Urusis Formation, Witputs subbasin, but a significant number, including Pteridinium, are from the Kliphoek Member, Zaris Formation, and the Neiderhagen Member, Nudaus Formation, north of the Osis arch, which separates the two subbasins. We extend the stratigraphic ranges and geographic distributions of several important taxa, including Archaeichnium, Ernietta, Pteridinium, and Swartpuntia, provide reassessments of the paleobiology of these and other organisms, and describe a new sponge—possibly an unmineralized archaeocyath—Arimasia germsi n. gen. n. sp. We also describe and illustrate various ichnofossils (including the oldest known traces from the Nama Group), narrow down the first appearance of Treptichnus in the Nama succession, and reinforce the idea that there was a prolific infauna of micrometazoans during the latest Ediacaran by naming and describing previously reported microburrows found on the surfaces of gutter casts as Ariichnus vagus n. igen. n. isp.

UUID: http://zoobank.org/8c267425-135a-4b0a-98b6-cf726515cbf2

The ontogeny of two species of corynexochid trilobites from the middle Cambrian Mount Cap Formation of the eastern Mackenzie Mountains, northern Canada, is documented. Sahtuia carcajouensis (Dolichometopidae) and Mackenzieaspis parallelispinosa (Zacanthoididae) are both endemic to this formation and only known from one locality. They, along with several other corynexochid taxa, occur in a succession of mudstone with scattered carbonate interbeds, deposited in a weakly storm-agitated setting near the flank of a semi-enclosed basin. The ontogeny of both species is characterized by mainly normal cranidial development, but a unique distribution of segments in their thoraxes and pygidia. The number of trunk segments was typical for their respective families, whereas the final number of segments released into the thorax was reduced. This occurred in both species through timing modifications to segment release, indicating heterochrony. Sahtuia carcajouensis and Mackenzieaspis parallelispinosa are likely derived from two separate clades, and heterochrony probably arose separately but synchronously. The endemicity of both species probably reflects unique paleoecological conditions in this part of the basin. Preliminary results indicate that the fossil-bearing mudstone was deposited under well-oxygenated conditions that underwent high nutrient flux and possibly experienced varying salinity. These factors may have affected the organisms’ physiology, or perhaps provoked an adaptation to achieve early maturation.

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.

The Ediacaran Subcommission of the International Commission on Stratigraphy is diligently working toward the goal of subdividing the Ediacaran Period into precise and useful chronostratigraphic units. As emphasized by Xiao and colleagues in 2016, one of the most effective tools in this endeavor will be the use of index fossils. Our special issue serves as a presentation of ongoing research efforts aimed at advancing this task and contains explorations into taxonomy, taphonomy, and the diversity of life during the Ediacaran Period.

First-formed shells of several species of Dalmanellidae (Brachiopoda) from the Ordovician (Katian) of North America were measured and compared: Cincinnetina multisecta, Diceromyonia tersa, Diceromyonia storeya, Paucicrura corpulenta, Paucicrura rogata, and Paucicrura sillimani. Sizes and structures of the first-formed shells suggest that members of this family had planktotrophic subadults, with some species showing indications of only an unshelled larval stage and others showing both a larval stage and a shelled juvenile stage. This differs from modern rhynchonelliformean brachiopods, which all possess only a lecithotrophic larval stage. The range of sizes of first-formed shells of most studied species are similar, but P. sillimani of Baffin Island, Canada (middle Katian), has a significantly larger first-formed shell that formed during an extended juvenile stage. This may have enabled the species to colonize newly exploitable habitats during an interval of rapid sea level rise in Laurentia during the Katian. This plasticity of developmental modes in the Dalmanellidae shows not only that using distantly related modern brachiopods as an analog for extinct Paleozoic lineages may be misleading, but also that development can vary within a single lineage and that timing of developmental stages should not be considered a reliable character for use in phylogenetic studies of brachiopods.

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.

A new genus and species of arachnid (Chelicerata: Arachnida), Douglassarachne acanthopoda n. gen. n. sp., is described from the late Carboniferous (Moscovian) Coal Measures of the Mazon Creek Lagerstätte, Illinois, USA. This is a unique animal with distinctive large spines on the legs. It has a subovate body, a segmented opisthosoma, and a terminal anal tubercle. The legs are robust and appear to have been similar in construction throughout the limb series, with heavy spination of the preserved proximal podomeres. The mouthparts and coxo-sternal region are equivocal. The preserved character combination does not permit easy referral to any known arachnid order, living or extinct, thus the new fossil in placed as Arachnida/Pantetrapulmonata incertae sedis. It contributes to an emerging pattern of disparate body plans among late Carboniferous arachnids, ranging from anatomically modern members of living orders through to extinct taxa, such as the present fossil, whose phylogenetic position remains unresolved.

UUID: http://zoobank.org/b70f5f95-9c8b-4389-bee5-b6031bff2ee2

The Cambrian dokimocephalid trilobite genus Deckera Frederickson, 1949 is a minor component of Steptoean (Jiangshanian) faunas of Laurentian North America. The original diagnosis emphasized strongly inflated palpebral areas of fixed cheeks and elevated palpebral lobes as important and novel characters. An appraisal of archival and new specimens from Oklahoma, Missouri, Pennsylvania, Nevada, Utah, and Newfoundland show that the genus is geographically widespread and likely represented by as many as nine species, although only two of them are named formally. Deckera cf. D. aldenensis Frederickson, 1949 from Nevada extends the stratigraphic range of Deckera down to the base of the Jiangshanian Stage, and new species from Nevada and Newfoundland take the genus down farther, into upper Paibian strata. Paibian species show that some basal members of the genus have weakly inflated, nearly flat palpebral areas with palpebral lobes that sit well below the crest of the glabella. A revised diagnosis of Deckera focuses on the broad cranidium with width across the palpebral lobes much greater than the sagittal length. Pygidia are known for a few species and all of them have an unusual flexure of the posterior margin and border. Lectotype and paralectotype specimens are designated for Deckera completa.

Encompassing global cooling, the spread of grasslands, and biogeographic interchanges, the Hemphillian North American Land Mammal Age is an important interval for understanding the factors driving ecological and evolutionary change through time. McKay Reservoir near Pendleton, Oregon is a natural laboratory for analyses of these factors. It is remarkable for its small vertebrate fauna including rodents, bats, turtles, and lagomorphs, but also for its larger mammal fossils like camelids, rhinocerotids, canids, and felids. Despite the importance of the site, few revisions to its faunal list have been published since its original description. We expand on this description by identifying taxa not previously known from McKay Reservoir based on specimens collected during fieldwork and through reidentification of previously collected fossils. Newly identified taxa include the borophagine canid Borophagus secundus (Matthew and Cook, 1909), the camelids Megatylopus Matthew and Cook, 1909 and Pleiolama Webb and Meachen, 2004, a dromomerycid, and the equids Cormohipparion Skinner and MacFadden, 1977 and Pseudhipparion Ameghino, 1904. Specimens previously assigned to Neohipparion Gidley, 1903 and Hipparion de Christol, 1832 lack the features necessary to diagnose these genera, which are therefore removed from the site's faunal list. The presence of Borophagus secundus, Cormohipparion, and Pseudhipparion is especially important, because each occurrence represents a major geographic range extension. This refined understanding of the fauna lays the foundation for future studies of taphonomy, taxonomy, functional morphology, and paleoecology—potentially at the population, community, or ecosystem levels—at this paleobiologically significant Miocene locality.

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.

Tribrachidium heraldicum Glaessner in Glaessner and Daily, 1959 is a triradial Ediacaran organism found in abundance within the Ediacara Member of the Flinders Ranges, South Australia. Here we report and describe a new species within the genus Tribrachidium Glaessner in Glaessner and Daily, 1959: Tribrachidium gehlingi new species from Nilpena Ediacara National Park (NENP), South Australia. Tribrachidium gehlingi n. sp. has low relief and three slightly curved, main arm-like structures that leave a conspicuous gap between the end of the arm-like structures and rim. In place of the ‘bulla’ found on T. herladicum, there are three secondary arm-like structures approximately half of the length of the main arm-like structures. Key morphological differences between the two species are statistically significantly different. Additionally, the species occur together within the same fossiliferous event horizons, indicating that the observed morphological differences are unlikely a result of taphonomy.

UUID: http://zoobank.org/196bef68-54da-42a9-9327-dcb55411a457

The Eager Formation (Cambrian Stage 4) of the Cranbrook area, British Columbia, contains abundant, sometimes beautifully preserved, trilobites and rare non-biomineralized taxa. Trilobites were first reported just over a century ago but have received little research attention, resulting in uncertainty in the number and identity of species within the assemblage and ambiguity in the age of the fauna. The trilobites of the Eager Formation in the Cranbrook area are described herein based largely upon material collected in 2015. A minimum of eight (and perhaps up to 11) trilobite species are recognized. The four species of olenelloids (Olenellus santuccii Webster n. sp., Olenellus? schofieldi, Mesonacis eagerensis, and Wanneria cranbrookense Webster n. sp.) are by far the most abundant elements of the fauna. At least two, and perhaps as many as five, species of dorypygid are present, as are two species of “ptychoparioids”. Paucity and poor preservational quality of specimens mean that the various dorypygid and “ptychoparioid” species are left in open nomenclature. Trilobite diversity in the Cranbrook Lagerstätte is comparable to that within other Lagerstätten from Cambrian Stage 4 (Series 2) of Laurentia. The diversity and abundance of trilobites, combined with biostratinomic and trace fossil data, suggest that the assemblage is autochthonous and/or parautochthonous, and that the local environment was at least periodically able to support a “typical” benthic trilobite community. The age of the Cranbrook Lagerstätte is constrained to lie within the middle Dyeran Stage of Laurentia, within what was a substantial stratigraphic gap in the distribution of Burgess Shale-type Lagerstätten.

UUID: http://zoobank.org/5beab9df-6b6a-4d6d-95e8-57057cd47a66

Natural history museums house numerous previously undescribed species and unknown information hidden in their collections. We describe lower Carboniferous slit-bearing gastropods (order Pleurotomariida, subclass Vetigastropoda; and family Goniasmatidae, subclass Caenogastropoda) from previously unreported gastropod collections made by Jane Longstaff (Jane Donald), one of the pioneering paleontologists of Paleozoic gastropods in the late nineteenth and early twentieth centuries. The gastropods were collected from the Lower Limestone Formation (Visean, Brigantian) near Dalry, Ayrshire, Scotland. The collection consists largely of microgastropods, many of which are unusually well-preserved including delicate ornament and protoconchs (larval shells). Three new pleurotomariidan species are described—Biarmeaspira heidelbergerae new species, Neilsonia seussae new species, Tapinotomaria longstaffae new species—in addition to seven species belonging to Borestus Thomas, 1940, Stegocoelia (Stegocoelia) Donald, 1889, Stegocoelia (Hypergonia) Donald, 1892, Donaldospira Batten, 1966, and Platyzona Knight, 1945. The caenogastropod-type protoconch is documented for the first time in Hypergonia, which is therefore placed in Goniasmatidae. The new data confirm that Neilsonia Thomas, 1940 (type genus of Neilsoniinae) belongs to Pleurotomariida and is distinct from the morphologically convergent Peruvispira Chronic, 1949 (Goniasmatidae). The selenizone morphology is identical in Biarmeaspira Mazaev, 2006 and Baylea de Koninck, 1883 during their early ontogeny, and Biarmeaspira develops an angulation on the selenizone (the diagnostic feature) in late ontogeny. This corroborates earlier suggestions that Biarmeaspira evolved from Baylea. Biarmeaspira heidelbergerae n. sp. is the first Carboniferous record of Biarmeaspira, which was previously only known from the Permian. The angulated selenizone evidently evolved several times in Pleurotomariida and the repeated appearance of this character in different groups (e.g., Phymatopleuridae, Eotomariidae, Pleurotomariidae) needs further studies using phylogenetic methods.

UUID: http://zoobank.org/92ae9a99-5774-4ee9-bf5d-9a9319494ef6

This work presents a detailed taxonomic study on organic-walled microfossils from the Ediacaran Sete Lagoas Formation (Bambuí Group) at the Barreiro section in the Januária area of the São Francisco basin, Brazil. Seven species are described, including Siphonophycus robustum (Schopf, 1968), Ghoshia januarensis new species, Leiosphaeridia crassa (Naumova, 1949), Leiosphaeridia jacutica (Timofeev, 1966), Leiosphaeridia minutissima (Naumova, 1949), Leiosphaeridia tenuissima Eisenack, 1958, and Germinosphaera bispinosa Mikhailova, 1986. These taxa are recovered for the first time in the Sete Lagoas Formation. They occur abundantly in the lower portion of the studied section, but only Ghoshia januarensis is present in the upper part of the studied section, probably due to environmental or taphonomic changes. Leiosphaeridia species, particularly Leiosphaeridia minutissima, dominate the organic-walled microfossil assemblage. Although most taxa described here have long stratigraphic ranges, they are consistent with a terminal Ediacaran age as inferred from detrital zircon data and tubular fossils (e.g., Cloudina and Corumbella) from the Sete Lagoas Formation.

UUID: http://zoobank.org/7f92b900-0176-4da6-93a3-fd51edb22cbf

Silicified brachiopods from Hirnantian strata in three sections of the lower Whittaker Formation, Mackenzie Mountains, northwestern Canada, yielded a moderately diverse, Edgewood-type Hirnantian fauna, consisting of 13 species: Biparetis paucirugosus, Brevilamnulella laevis, Dalmanella edgewoodensis, Drabovia noixella, Eospirigerina putilla, Epitomyonia paucitropida, Epitomyonia sekwiensis, Glyptorthis papillosa new species, Gnamptorhynchos orbiculoidea, Katastrophomena mackenzii new species, K. parvicardinis, Parastrophina cf. P. minor, and Skenidioides sp. Compared to the typical Edgewood fauna of the American Midcontinent, Brevilamnulella laevis has a notably smaller shell than B. thebesensis, and is interpreted as a deeper-water form. The strong faunal affinity of the Mackenzie Mountains fauna to the Edgewood-type Hirnantian fauna is indicated by the occurrence of Biparetis, Brevilamnulella, Eospirigerina, and Gnamptorhynchos. In addition to the Edgewood type area within Laurentia, Biparetis, Eospirigerina, and Gnamptorhynchos are characteristic taxa that also occur in the Ellis Bay Formation (Hirnantian) of Anticosti Island. Multivariate and network analyses strongly support the differentiation between an Edgewood-type Hirnantian fauna in Laurentia and peri-Laurentia and the typical Hirnantia fauna of the Kosov Province in Gondwana, peri-Gondwana, South China, Kazakhstan terranes, Avalonia, and Baltica.

UUID: http://zoobank.org/7ff8f8c8-52d1-4527-acae-9bacd2e8b914

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

A new cornulitid genus and species, Porkuniconchus fragilis new genus and species, is here described from the Ärina Formation (Hirnantian, Porkuni Regional Stage) of northern Estonia. This new taxon differs from most cornulitids by having a fusiform ornamentation pattern that is somewhat similar to that of Kolihaia. All studied specimens are attached to a carbonate hardground. The hardground fauna is by abundance and encrustation area dominated by cornulitids. Other encrusters are represented only by a single sheet-like cystoporate bryozoan. The cornulitid specimens represent different growth stages, which suggest that the hardground was continuously colonized by cornulitid larvae. The high encrustation density indicates that the studied hardground may have represented a high-productivity site in the Hirnantian of the Baltic Basin.

UUID: http://zoobank.org/623afcc3-ab32-4e8f-be14-a1093cba4ae6

Paraconularia planicostata (Dawson, 1868) is one of two species in this genus (Sinclair, 1940) of conulariid cnidarian currently known from Mississippian strata in the Maritimes Basin in Atlantic Canada (Babcock and Feldmann, 1986). A salient characteristic of the species is the presence of a low and narrow internal carina at or near the longitudinal midline of each of the four faces of the gently tapered periderm (Van Iten et al., 2020). Paraconularia planicostata occurs in marine carbonates in the Upper Mississippian lower Windsor and lower Codroy groups in Nova Scotia and western Newfoundland, respectively (e.g., Bell, 1929; Stacy, 1953; Dix and James, 1988; Boehner et al., 1989; Boehner and Prime, 1993; Lavoie and Sami, 1998; Jutras et al., 2006; Ryan and Giles, 2017; Van Iten et al., 2020). The species is exceptionally abundant, with richly fossiliferous biohermal limestones containing up to approximately 20 specimens per 1000 cm3 of host rock (Van Iten, unpublished observations)—a volumetric density matched by few other conulariid-bearing rock units.

The Jurassic trigoniid bivalves of Gebel Maghara, northern Sinai, Egypt are described and figured. They belong to 14 species, nine genera, and two families. The identified taxa occur in rocks ranging in age from the Toarcian (Lower Jurassic) to the lower Kimmeridgian (Upper Jurassic). Five genera and one species are new: Magharitrigonia asymmetrica new genus new species; Cotswoldella aff. C. hemisphaerica (Lycett, 1853); Cornbrashella pullus (J. de C. Sowerby, 1826); Parorthotrigonia lepidomorpha (Abdallah and Fahmy, 1969); and Retetrigonia imbricata (J. de C. Sowerby, 1826). Five species, Trigonia reticulata Agassiz, 1840, T. cf. T. castor d'Orbigny, 1849, Promyophorella tuberculata (Agassiz, 1840), Orthotrigonia exortiva (Kitchin, 1903), and O. gracilis (Kitchin, 1903) are recorded from the Jurassic rocks of Gebel Maghara for the first time.

UUID: http://zoobank.org/4dc3cc67-6bc3-406f-a022-6a05ed97efc6

We report new material of the rare early Eocene rodent Lophiparamys debequensis Wood, 1962 from the Willwood Formation of the southern Bighorn Basin, north-central Wyoming. The new material constitutes the first record of L. debequensis from the Bighorn Basin and documents aspects of the anatomy of Lophiparamys that were previously unknown, including a portion of the maxilla and a portion of the tarsus. The maxillary fragment demonstrates that Lophiparamys has a small P3 and a relatively large infraorbital canal. The tarsus of Lophiparamys is similar to that of other early rodents but differs in a few features that suggest an arboreal locomotor repertoire, including an asymmetric astragalar trochlea, long astragalar neck, transverse astragalar sustentacular facet, short calcaneal tuber, elongate calcaneal ectal facet, and circular calcaneal cuboid facet. The presence of arboreally adapted features in the tarsus of Lophiparamys is consistent with a hypothesized relationship between small-bodied Eocene microparamyine rodents and extant Gliridae. Phylogenetic analysis fails to consistently support this relationship or monophyly of Microparamyinae, but both remain plausible. Comparison of L. debequensis with other species of the genus emphasizes the distinctiveness of L. debequensis and suggests the presence of multiple lineages of Lophiparamys.