The tectonic evolution of the Sibumasu Block during the Permian remains controversial, and Permian faunas and their paleobiogeographic affinities provide some insight into its paleogeographic and tectonic evolutionary histories. In this paper, a new brachiopod fauna dominated by Spinomartinia prolifica Waterhouse, 1981 is described from the uppermost part of the Taungnyo Group in the Zwekabin Range, eastern Myanmar. This brachiopod fauna includes 23 species and its age is well constrained as late Kungurian by the associated conodonts, i.e., Vjalovognathus nicolli Yuan et al., 2016 and Mesogondolella idahoensis (Youngquist, Hawley, and Miller, 1951), contrary to the late Sakmarian age given to the same brachiopod faunas previously reported from southern Thailand and Malaysia. Based on comprehensive comparisons of the Cisuralian brachiopod faunas and other data in different parts of the Sibumasu Block, we consider that they are better subdivided into two independent stratigraphic assemblages, i.e., the lower (earlier) Bandoproductus monticulus-Spirelytha petaliformis Assemblage of a Sakmarian to probably early Artinskian age, and the upper (younger) Spinomartinia prolifica-Retimarginifera alata Assemblage of a late Kungurian age. The former assemblage is a typical cold-water fauna, mainly composed of Gondwanan-type genera, e.g., Bandoproductus Jin and Sun, 1981, Spirelytha Fredericks, 1924, and Sulciplica Waterhouse, 1968. The latter assemblage is strongly characterized by an admixture of both Cathaysian and Gondwanan elements, as well as some genera restricted to the Cimmerian continents. Notably, the spatial distribution pattern of these two separate brachiopod assemblages varies distinctly. The Sakmarian cold-water brachiopod faunas have been found in association with glacial-marine diamictites throughout the Sibumasu Block including both the Irrawaddy and Sibuma blocks. In contrast, the Kungurian biogeographically mixed brachiopod faunas are only recorded in the Irrawaddy Block, unlike the Sibuma Block that contains a contemporaneous paleotropical Tethyan fusuline fauna. Thus, it appears likely that by the end of Cisuralian (early Permian), the Sibumasu Block comprised the Irrawaddy Block in the south with cool climatic conditions, and the Sibuma Block in the north with a temperate to warm-water environment, separated by the incipient Thai-Myanmar Mesotethys.

The lower strata of the Umachiri Formation from the Altiplano of southeast Peru have yielded a brachiopod-dominated assemblage, containing representatives of the brachiopod superfamilies Polytoechioidea, Orthoidea, and Porambonitoidea, as well as subsidiary trilobite and echinoderm remains. Two new polytoechioid genera and species, Enriquetoechia umachiriensis new genus new species and Altiplanotoechia hodgini n. gen. n. sp. Colmenar in Colmenar and Hodgin, 2020, and one new species, Pomatotrema laubacheri n. sp., are described. The presence of Pomatotrema in the Peruvian Altiplano represents the occurrence at highest paleolatitude of this genus, normally restricted to low-latitude successions from Laurentia and South China. Other polytoechioids belonging to Tritoechia (Tritoechia) and Tritoechia (Parvitritoechia) also occur. Identified species of orthoids from the genera Paralenorthis, Mollesella, and Panderina? occur in the Peruvian Cordillera Oriental and in the Argentinian Famatina Range. The only porambonitoid represented is closely related to Rugostrophia latireticulata Neuman, 1976 from New World Island, interpreted as peri-Laurentian. These brachiopod occurrences indicate a strong biogeographic affinity of the Peruvian Altiplano with the Famatina and western Puna regions, suggesting that the brachiopod faunas of the Peruvian Altiplano, Famatina, and western Puna belonged to a well-differentiated biogeographical subprovince during the Early–Middle Ordovician on the margin of southwestern Gondwana. Links with peri-Laurentian and other low-latitude terranes could be explained by island hopping and/or continuous island arcs, which might facilitate brachiopod larvae dispersal from the Peruvian Altiplano to those terranes across the Iapetus Ocean. Brachiopods from the lower part of the Umachiri Formation indicate a Floian–?Dapingian age, becoming the oldest Ordovician fossils of the Peruvian Altiplano.

UUID: http://zoobank.org/9670a000-260d-4d75-9261-110854c7afb8

New linguliform microbrachiopods from the Middle Ordovician are described and illustrated. This fauna was recovered from the uppermost beds of the San Juan Formation in two sections of the Central Precordillera (Argentina), which are accurately dated to the Lenodus pseudoplanus Zone (middle Darriwilian). The fauna consists of the obolid Luthieria diminuta n. gen. n. sp., and the acrotretids Eoconulus tucunucoensis n. sp., Conotreta andina Lavié, Serra, and Feltes, Scaphelasma zharykensis Popov, and Numericoma rowelli Holmer et al. This low-diversity lingulate association displays close similarities with coeval faunas that inhabited the Laurentia, Baltica, and Kazakhstanian regions, in agreement with evidence from other linguliform and rhynchonelliform brachiopods.

UUID: http//zoobank.org/fe9acbb0-6654-4462-ba4d-ea2386ae79f6

The end-Ordovician mass extinction, linked to a major glaciation, led to deep changes in Hirnantian–Rhuddanian biotas. The Hirnantia Fauna, the first of two Hirnantian survival brachiopod-dominated communities, characterizes the lower–mid Hirnantian deposits globally, and its distribution is essential to understand how the extinction took place. In this paper, we describe, illustrate, and discuss the first macrofossiliferous Hirnantia Fauna assemblage from Belgium, occurring in the Tihange Member of the Fosses Formation at Tihange (Huy), within the Central Condroz Inlier. Six fossiliferous beds have yielded a low-diversity, brachiopod-dominated association. In addition to the brachiopods (Eostropheodonta hirnantensis, Plectothyrella crassicosta, Hirnantia sp., and Trucizetina? sp.), one trilobite (Mucronaspis sp.), four pelmatozoans (Xenocrinus sp., Cyclocharax [col.] paucicrenulatus, Conspectocrinus [col.] celticus, and Pentagonocyclicus [col.] sp.), three graptolites (Cystograptus ancestralis, Normalograptus normalis, and ?Metabolograptus sp.), together with indeterminate machaeridians and bryozoans were identified. The graptolite assemblage, from the Akidograptus ascensus-Parakidograptus acuminatus Biozone, indicates an early Rhuddanian (Silurian) age, and thus, an unexpectedly late occurrence of a typical Hirnantia Fauna. This Belgian association may represent an additional example of relict Hirnantia Fauna in the Silurian, sharing characteristics with the only other known from Rhuddanian rocks at Yewdale Beck (Lake District, England), although reworking has not been completely ruled out. The survival of these Hirnantian taxa into the Silurian might be linked to delayed post-glacial effects of rising temperature and sea-level, which may have favored the establishment of refugia in these two particular regions that were paleogeographically close during the Late Ordovician–early Silurian.

Devonian orthotetides from South America have often been uncritically assigned to a limited number of broadly described species. Schellwienella clarkei n. sp. is described from the Ponta Grossa Formation, Paraná Basin, southern Brazil. These brachiopods had been identified as Schuchertella agassizi. Schellwienella clarkei n. sp. differs from Schuchertella agassizi on the basis of shell structure, dental plates, and cardinalia.

UUID: http://zoobank.org/90ebc242-42c3-4bd7-9b63-461df05b6f28

The lower Famennian ‘Cyrtospirifer’ orbelianus brachiopod Zone established in Armenia by Abrahamyan (1957) (coeval to the crepida conodont Zone) contains an abundant and diverse brachiopod fauna that still remains poorly studied. In an effort to revise and update its systematic classification and to assess the brachiopod diversity in this area after the Kellwasser extinction event at the end of the Frasnian, our attention is here focused on rhynchonellides and athyrides. Six rhynchonellide species are described belonging to five genera as well as a single athyride species (Crinisarina pseudoglobularis n. sp.), which is new to science. The genus Crinisarina is reported for the first time in the South Armenian Block (SAB), which was then part of the northern margin of Gondwana. Some of the rhynchonellides identified were previously recognized in this area, but they require modern documentation and taxonomic reassessment. More particularly, it is the first time that the internal structure of Sartenaerus baitalensis (Reed, 1922) is illustrated, taking into account that it is the type species of a biostratigraphically significant Famennian genus. One of the oldest punctate rhynchonellide species, Greira transcaucasica Erlanger, 1993, is described for the first time from Armenia and its intraspecific morphological variability is documented quantitatively. From a paleobiogeographic viewpoint, the studied brachiopod fauna clearly shares affinities with contemporaneous ones from other regions of the Gondwanan northern margin that extend eastwards of the SAB to Afghanistan and Pamir, although there are also some endemic elements.

UUID: http://zoobank.org/798eb5f9-ad15-4d90-bc6a-ff22ee936438

We describe two new genera of Triassic Aviculopectinoidea: Cristaflabellum n. gen., which is biconvex and has a strongly plicate shell, and Globodiscus n. gen., which is equiconvex and externally smooth or nearly so. Globodiscus contains the new species G. kiliani n. gen. n. sp. and G. vinzenti n. gen. n. sp. In order to make the taxonomic concept of the superfamily Aviculopectinoidea more consistent with that of its sister group Pectinoidea (scallops), we use tribes rather than families or subfamilies for accommodating the new taxa. Cristaflabellum is placed in the tribe Antijanirini (previously family Antijaniridae), whereas Globodiscus is made the type genus of the new tribe Globodiscini. Both tribes are placed within the family Aviculopectinidae, which is revised to include both equiconvex and inequiconvex taxa. We suggest that tribes are a more appropriate taxonomic rank for many of the previously erected species-poor families and subfamilies of Aviculopectinoidea.

UUID: http://zoobank.org/d143663a-9016-459f-8e24-660102adcf6a

Hexangulaconulariids (Cambrian stages 1–2) are an extinct group of medusozoan polyps having a biradially symmetrical, fan-shaped periderm that is distinct from those of medusozoan polyps showing three-, four-, five-, or six-fold radial symmetry. Hexangulaconulariids exhibit substantial variation in gross morphology, including variation in the number of faces on each of the two major sides of the periderm. An intermediate taxon of hexangulaconulariids with ten faces (five on each major side) was expected. Here we describe a new hexangulaconulariid, Decimoconularia isofacialis new genus new species from Bed 5 of the Yanjiahe Formation (Cambrian Stage 2) in the Three Gorges area of Hubei Province, China. The new taxon differs from other hexangulaconulariids (Arthrochites, Hexaconularia, and Septuconularia) mainly in possessing a total of ten faces. The two lateral margins are each marked by a ridge in about the apertural half of the periderm and by a collinear furrow in about the apical half, while the five faces on each major side are bounded by a furrow in about the apertural half and by a collinear ridge in about the apical half. Among hexangulaconulariids, Decimoconularia and Septuconularia may be more closely related to each other than either genus is to Arthrochites or Hexaconularia.

UUID: http://zoobank.org/ca270a3b-25ee-4d1f-bdeb-91a963370e70

Strata of the Solvik Formation in the central Oslo Region (upper Hirnantian through most of Aeronian) are very fossiliferous and provide a good record relating to the survival and recovery faunas after the end-Ordovician mass extinctions. The ribbed atrypide fauna is especially rich with 21 species present. Samples from most of these taxa have been sectioned to reveal internal structures for taxonomic study. Of these, 13 species belong to the family Atrypidae, three of which are described in the present paper; Dihelictera engerensis n. sp., Gotatrypa vettrensis n. sp., and Rhinatrypa henningsmoeni n. gen. The family Atrypidae follows a global pattern of recovery with an increase in diversity registered in upper Rhuddanian and further diversification in Aeronian strata. The focus of this paper is the family Atrypinidae, which shows a different pattern. They are common and fairly diverse near the base of the Rhuddanian in deeper waters and rare further up, especially in the Aeronian. One new genus, Bockeliena, and two new species, Plectatrypa rindi and Euroatrypa? sigridi are defined. The relationship between the subfamilies Spirigerininae and Plectatrypinae is clarified through thin sections of material from the Ordovician/Silurian boundary layers. The plectatrypids originated in Baltica through transitional species found in upper Katian to Hirnantian strata leading from the cosmopolitan Eospirigerina to the Plectatrypa lineage with imbricate ribbing and, separately, to Bockeliena and others with lamellose, widely spaced ornamentation. The Oslo Region probably acted as a nexus for survival and spread of brachiopods after the end-Ordovician mass extinction.

UUID: http://zoobank.org/95340b41-5537-4192-9338-211a2940bea8.

Protandrous sex change (sex change from male to female) is one of the diverse sexual expressions exhibited by bivalves, but its expression in the shell is quite rare. Previous studies on living and fossil astartids suggest a relationship between protandrous sex change and the formation of crenulations on the ventral shell margin at later ontogenetic stages. Here we report the formation of such crenulations in the Early Jurassic astartid Nicaniella rakoveci (Kuhn, 1935) from the Amaltheenton Formation at Buttenheim, Franconia. This is the earliest known record of protandrous hermaphroditism in fossil bivalves, predating previous reports by at least 13 Myr. A principal component analysis of linear size measurements and Fourier shape analysis of the shell outlines revealed that the outline of Nicaniella rakoveci specimens varies from subquadrate to subcircular, but this variation is independent of the presence or absence of crenulations and therefore not associated with sex. Crenulated specimens exhibit a lower height/inflation ratio than non-crenulated ones, suggesting that the protandrous females have more inflated valves than the males. The formation of crenulations was probably related to allocation of resources for reproduction. The most likely function of the crenulations was to increase the internal shell volume in the female stage to accommodate more eggs rather than being an adaptation against predation as often assumed for other bivalves. The formation of crenulations is part of the protandrous life history and probably is controlled by a genetic mechanism that is also responsible for sex change.

In order to maximize the utility of future studies of trilobite ontogeny, we propose a set of standard practices that relate to the collection, nomenclature, description, depiction, and interpretation of ontogenetic series inferred from articulated specimens belonging to individual species. In some cases, these suggestions may also apply to ontogenetic studies of other fossilized taxa.

Paleozoic scaphopods are among the most poorly known mollusks because of their featureless tubular shell morphology and fragmentary preservation. An apical orifice at the posterior end of a conch is a diagnostic character of Scaphopoda that distinguishes them from other groups of animals that produce similar calcareous tubes, but this structure is rarely preserved. A rich molluscan fauna from the Permian Akasaka Limestone in central Japan includes scaphopod shells, and past studies have reported four species, all of which were based on fragmentary specimens. This study recognizes six species in the Akasaka Limestone mainly on the basis of museum/institution collections, and a new genus (Minodentalium) and three species (Prodentalium onoi, M. hayasakai, and M. okumurai) are described, two known species (P. akasakensis and P. neornatum) are redescribed in more detail, and one species (Prodentalium sp.) is described under open nomenclature. The following eight known species are allocated to the new genus Minodentalium: Plagioglypta furcata Waterhouse, 1980; Pl. girtyi Knight, 1940; Pl. subannulata Easton, 1962; Dentalium ingens De Koninck, 1843; D. meekianum Geinitz, 1866; Pl. prosseri Morningstar, 1922; Dentalium priscum Münster in Goldfuss, 1842; and D. herculeum De Koninck, 1863. All the species, except for M. hayasakai, are gigantic, reaching 200 mm or more in length. The species richness is the greatest known from a single locality/formation worldwide.

UUID: http://zoobank.org/35405b9d-3ba7-40bf-87c5-3f2b550b1a6d

The filter-feeding organ of some extinct brachiopods is supported by a skeletal apparatus called the brachidium. Although relatively well studied in Atrypida and Athyridida, the brachidial morphology is usually neglected in Spiriferida. To investigate the variations of brachidial morphology in Spiriferida, 65 species belonging to eight superfamilies were analyzed. Based on the presence/absence of the jugal processes and normal/modified primary lamellae of the spiralia, four types of brachidium are recognized. Type-I (with jugal processes) and Type-II (without jugal processes), both having normal primary lamellae, could give rise to each other by losing/re-evolving the jugal processes. Type-III, without jugal processes, originated from Type-II through evolution of the modified lateral-convex primary lamellae, and it subsequently gave rise to Type-IV by evolving the modified medial-convex primary lamellae. The evolution of brachidia within individual evolutionary lineages must be clarified because two or more types can be present within a single family. Type-III and Type-IV are closely associated with the prolongation of the crura, representing innovative modifications of the feeding apparatus in response to possible shift in the position of the mouth towards the anterior, allowing for more efficient feeding on particles entering the mantle cavity from the anterior gape. Meanwhile, the modified primary lamellae adjusted/regulated the feeding currents. The absence of spires in some taxa with Type-IV brachidium might suggest that they developed a similar lophophore to that in some extant brachiopods, which can extend out of the shell.

A new sinistrally coiled univalved mollusk Catalanispira n. gen. is described with two species; Catalanispira reinwaldti (Öpik, 1930) from the Middle Ordovician Kõgekallas Formation (Darriwilian) of Estonia and Catalanispira plattevillensis n. gen. n. sp. from the Upper Ordovician Platteville Formation (Sandbian) of northern Illinois, USA. Morphological features include a large, low-trochiform shell, a narrow lenticular aperture, a deep funnel-like umbilicus, a falcate inner lip and a large (1.4 mm wide) protoconch. Ornamentation consists of fine commarginal growth lines or ribs but superimposed on a slightly irregular shell surface. Catalanispira n. gen. is placed within the sinistrally coiled order Mimospirida and the family Onychochilidae, and Catalanispirinae n. subfam. is proposed. The large Lower Ordovician (Tremadocian) Pelecyogyra Ebbestad and Lefebvre, 2015 from Morocco and France is transferred to this new subfamily. The well-preserved initial growth stage of Catalanispira plattevillensis n. gen. n. sp. is cap-shaped, slightly asymmetrical, unusually large, and smooth, and represents either an unusually large embryonic shell (protoconch 1) or a larval shell (protoconch 2). It differs from the smaller protoconch described for the clisospirine Mimospira Koken in Koken and Perner, 1925, which might include a multiwhorled larval shell (protoconch 2). Mimospirids are dominantly Ordovician, and have been classified as untorted mollusks (only distantly related to gastropods), dextral hyperstrophic gastropods, or sinistral orthostrophic gastropods. Sinistral asymmetry already in the embryonic shell and lack of conclusive evidence for coiling direction, e.g., an operculum, could suggest that Catalanispira n. gen. or similar mimosprids were sinistral orthostrophic gastropods. Currently the group is therefore classified as a group of sinistral orthostrophic gastropods, unranked within the Gastropoda.

UUID: http://zoobank.org/affc8dcf-4c0f-493d-bee5-75a457996e84

Few bryozoans have been described from the Cretaceous Western Interior Seaway (WIS), which is consistent with the low diversity of other typically stenohaline groups in this large expanse of relatively shallow marine water. Here we describe a new cheilostome bryozoan, Conopeum flumineum n. sp., based on well-preserved material from the Campanian Judith River Formation of the Upper Missouri River Breaks National Monument in north-central Montana. The new species shows strong morphological similarities with Conopeum seurati, a Recent species that is often categorized as brackish, but which is euryhaline and can also be found in marine and stenohaline environments. The new Campanian bryozoan species was found in a locality also containing fragmentary remains of dinosaurs and other terrestrial vertebrates, as well freshwater mollusks and terrestrial plant debris. The sedimentology and facies associations of the fossil-bearing site suggest that the depositional setting was a swamp or tidally influenced fluvial backwater on the Judith River coastal plain. The proximity of the site to the western shoreline of the WIS presumably made it susceptible to occasional marine flooding during storms or extreme tides. Previous occurrences of Conopeum in the Cretaceous of the Western Interior have also been associated with dinosaur remains, corroborating the very nearshore and at times even ‘upstream’ distribution of this euryhaline genus.

UUID: http://zoobank.org/bb1fdc8a-5017-44c5-9251-9e24ef3995e3.

New atopid trilobites are described from the early Cambrian Cumbres beds and Herrerías shale of northern Huelva Province (Andalusia, Spain) and are dated as middle–late Marianian (Cambrian Series 2, Stage 4). New specimens of Atops calanus Richter and Richter, 1941 are described and the Laurentian species Pseudatops reticulatus (Walcott, 1890b) is recognized for the first time in the Mediterranean subprovince. The associated trilobite assemblage studied herein suggests an age close to the base of Cambrian Stage 4.

Although taxonomically distinct, the Cenozoic pleurotomariids are the bottlenecked remnants of the Mesozoic members of the family in terms of morphology, with only conical forms surviving the end-Cretaceous mass extinction. Here, we propose an updated classification scheme for the Cenozoic representatives of this group, based on data from the entire Cenozoic pleurotomariid fossil record. We consider all conventional as well as several new characters so that this scheme can readily help to distinguish Cenozoic pleurotomariid genera. Following the new classification scheme, a revision of the generic status of Cenozoic species previously assigned to ‘Pleurotomaria’ Defrance, 1826 is presented.

Only a few Cenozoic pleurotomariid gastropods have been reported from the Indian subcontinent. Here we report four species from the Oligocene of the Kutch Basin and the early Miocene (Burdigalian) of the Dwarka Basin of Gujarat, western India, of which two are described as new: Perotrochus bermotiensis n. sp., Entemnotrochus kathiawarensis n. sp., Entemnotrochus cf. E. bianconii, and Entemnotrochus? sp. 1.

UUID: http://zoobank.org/89b6ff67-2834-477f-862b-67691104aca4

We document and quantify one of the oldest predator–prey interactions between naticid gastropods and molluscan prey, on the basis of drill holes in shells, from the Late Jurassic (Oxfordian) beds of Kutch, western India. Previously, many workers recorded naticid-like drill holes on prey taxa from the Triassic and the Jurassic, but in the absence of associated naticid body fossils, they remained equivocal.

The present gastropod community is dominated by turritellines (98% of the sample) that form the turritelline-dominated assemblage, and the naticid drilling predation is restricted almost entirely to turritellines among gastropods. Confamilial naticid predation takes place occasionally. Within the bivalve community, corbulids and nuculids are most abundant and are drilled more often than other taxa. These observations indicate that prey selection was opportunistic and based solely on availability. Drilling intensities at both assemblage and lower taxon levels are low. Behavioral stereotypy of naticid predation in some cases is moderately high.

Turritellines are often the preferred prey of naticid gastropods since the late Early Cretaceous. These two groups form a recurrent association reflecting prey–predator interaction. Here we suggest that both turritellines and naticids evolved during the Jurassic, and the prey–predator interaction between them was established shortly thereafter. Among bivalves, corbulids also became important prey of naticids in the same spatiotemporal framework. Corbulids are older than naticids and first appeared during the Middle Jurassic. After their first encounter with naticids, corbulids evolved conchiolin layers within the valves to resist predation.

Bryozoans with calcified frontal shields formed by the fusion of costae, collectively constituting a spinocyst, are traditionally assigned to the family Cribrilinidae. Today, this family is regarded as nonmonophyletic. In the Argentine Cenozoic, cribrilinids were until recently represented by only two fossil species from the Paleocene of Patagonia. This study describes the first fossil representatives of Jolietina and Parafigularia: J. victoria n. sp. and P. pigafettai n. sp., respectively. A fossil species of Figularia, F. elcanoi n. sp., is also described. The material comes from the early Miocene of the Monte León and Chenque formations (Patagonia, Argentina). For comparison, we also provide redescriptions of the remaining extant species of Jolietina: J. latimarginata (Busk, 1884) and J. pulchra Canu and Bassler, 1928a. The systematic position of some species previously assigned to Figularia is here discussed. Costafigularia n. gen. is erected, with Figularia pulcherrima Tilbrook, Hayward, and Gordon, 2001 as type species. Two species previously assigned to Figularia are here transferred to Costafigularia, resulting in C. jucunda n. comb. and C. tahitiensis n. comb. One species of Figularia is reassigned to Vitrimurella, resulting in V. ampla n. comb. The family Vitrimurellidae is here reassigned to the superfamily Cribrilinoidea. The subgenus Juxtacribrilina is elevated to genus rank. Inferusia is regarded as a subjective synonym of Parafigularia. Parafigularia darwini Moyano, 2011 is synonymized with I. taylori Kuklinski and Barnes, 2009, resulting in Parafigularia taylori n. comb. Morphological data suggest that these genera comprise different lineages, and a discussion on the disparities among cribrilinid (sensu lato) spinocysts is provided.

UUID: http://zoobank.org/215957d3-064b-47e2-9090-d0309f6c9cd8

Olenellid trilobites from the lower Cambrian of the Iberian Peninsula are very scarce and poorly studied, making them difficult to compare with defined species and to include in biostratigraphic and paleobiogeographic analyses. Based on newly collected specimens, we revise the species ‘Callavia? lotzei’ Richter and Richter, 1941 from the ‘Cumbres beds’ of Cumbres de San Bartolomé and the ‘Herrerías shale’ of Cañaveral de León, Sierra del Bujo, and Hinojales (Huelva, Spain), and ‘Paradoxides choffati’ Delgado, 1904 from the Vila Boim Formation of Elvas (Portugal). The new material indicates that Callavia? lotzei is a junior synonym of ‘P. choffati.’ The Iberian species are here assigned to Callavia Matthew, 1897, for which morphological characters are reassessed, offering a valuable opportunity to discuss characters previously misinterpreted for this genus. Traditionally assigned to the Olenelloidea Walcott, 1890, Callavia lacks some of the diagnostic characters of this superfamily and is here assigned to Judomioidea Repina, 1979. A new diagnosis for this genus is provided, and Sdzuyomia Lieberman, 2001 is considered to represent a junior synonym of Callavia. The genus Callavia is distributed across the western margin of Gondwana, from the western Mediterranean region (Iberia and Morocco) throughout all the Avalonia sectors (UK, eastern Newfoundland, and Massachusetts). Its presence in Iberia supports the faunal links between the West Gondwana domain and Avalonia during Cambrian Series 2. The Iberian records of Callavia choffati are assigned to the middle part of the regional Marianian Stage (uppermost Cambrian Stage 3 to the lowermost Cambrian Stage 4) and correlates with the Callavia Biozone of Avalonia (lower Branchian Series).