Gap-coding permits the use of continuous metric characters in cladistic analyses. Character means are converted to integer equivalents by placing character state divisions in the locations of phenetic breaks between specimen clusters, under the assumption that these breaks represent the locations of bottlenecks in character distributions. Similarities and differences between specimens from closely related species of cystoporate bryozoans were evaluated for the first time by converting continuous morphometric measurements into gap-coded binary and multistate characters and analyzing them cladistically, rather than just phenetically, across multiple species of Strotopora, Cliotrypa ramosa and Fistulipora compressa.

Our results demonstrate that cladistic analysis of gap-coded morphological characters can be effective in resolving phylogenetic relationships at low taxonomic levels (within and among genera) while objectively highlighting both the morphological features that specimens (taxa) share and those characteristics that differentiate them. Differences in cystiphragm abundances and sizes, especially in the proximal portions of colonies, discriminate between species of Strotopora. Colony size and growth form, abundances and lengths of hemiphragms, and sizes of cystopores discriminate between Strotopora and the closely related genus Cliotrypa. Cladistic patterns indicate that Strotopora foveolata Ulrich is a valid species with Strotopora dermata as its junior subjective synonym. Fistulipora compressa is reassigned to the genus Strotopora whereas a decision on the taxonomic status of Cliotrypa ramosa requires a broader cladistic analysis of fistuliporine genera.

The Murfreesboro Limestone and the succeeding Pierce Limestone (Black Riveran, Middle Ordovician) of the Stones River Group, the oldest rocks exposed in central Tennessee, contain a fossil invertebrate fauna including bryozoans. Bryozoans are relatively scarce in the Murfreesboro Limestone but are abundant in the overlying Pierce Limestone. The bryozoan fauna includes the cryptostomes, Escharopora, Graptodictya, Pachydictya, Phylloporina, Stictopora, Stictoporella, Trigonodictya, Ulrichostylus; the trepostomes Amplexopora, Batostoma, Hemiphragma, Nicholsonella, Parvohallopora; and the cystoporates Ceramophylla and Constellaria. These bryozoans are the oldest known in Tennessee and are the only early Black Riveran assemblage in North America described at the species level. Species of Nicholsonella, Pachydictya, and Stictopora in the Murfreesboro and species of Constellaria and Phylloporina? in the Pierce are closely related to those found in rocks of Chazyan age in New York and Vermont. Species of Ceramophylla, Escharopora, and Trigonodictya in the Pierce Limestone of central Tennessee are decidedly similar to species found in Black Riveran strata of New York. The stratigraphic ranges, geographic distribution, and taxonomy of previously described species from Tennessee are updated.

Cythere ikeyanoriyukii n. sp., an extant phytal ostracode genus, was obtained from the Middle Eocene McIntosh Formation in the Doty Hills, western Washington State, USA. It was associated with eleven taxa, which are extant phytal and shelfal genera such as Loxocorniculum, Xestoleberis, Ambostracon, Coquimba, and Acanthocythereis. The presence of Cythere in this assemblage is surprising and indicates that the first appearance of this genus was middle Eocene time at the latest, or at least 20 Ma earlier than previously thought. Cythere did not originate in the Pacific Ocean around Japan as previously thought, but instead must have migrated from the northeastern Pacific to the northwestern Pacific between middle Eocene and early Miocene time.

The Cincinnatian (Katian) of the Cincinnati Tri-State area is widely regarded as one of the most fossiliferous sections known (Meyer and Davis, 2009). Echinoderms from these strata include well-described asteroids, crinoids, cyclocystoids, edrioasteroids, glyptocystoids, mitrates, and ophiuroids. John Pope discovered a partially articulated echinoderm in float from the Fairview Formation that does not correspond to any known Cincinnatian echinoderm. Although mentioned in Ubaghs (1966, as a presumable personal communication from Pope, 1960), Haude and Langenstrassen (1976), Reich (2001), and Reich and Haude (2004), this specimen at the Cincinnati Museum Center (CMCPIP 51316) has neither been described nor illustrated; yet, these authors attributed it to Volchovia Hecker, 1938 in the Class Ophiocistioidea. Questions swirl around this fossil: what is its complete morphology; does it belong to Volchovia; whether or not it can be assigned to Volchovia, is it an ophiocistioid? The first step to understand this enigmatic echinoderm is to illustrate and describe the specimen, which is the objective of this note.

The silurian graptoloid genus Globosograptus was erected by Boucek and Přibyl (in Přibyl 1948, p. 37), who selected as type species Monograptus wimani Bouček, 1932. As noted by Bulman and Rickards in the Treatise (Bulman 1970, p. V155), Globosograptus “was based on the silhouette appearance of a slender Llandovery species on which the thecae possess a long prothecal portion, no thecal overlap, and a seemingly enrolled methathecal portion. The nature of this enrollment is indefinite … The genus has no precise significance and its application is quite impracticable.”

Closterocrinus elongatus Hall, 1852, long assigned to the cladid inadunate crinoid family Ampheristocrinidae (=Euspirocrinidae), has been found to possess pinnulate biserial arms and a cup composed of four exsert basals, five radials, a primanal above the radial circlet, and fixed primibrachials and secundibrachials. Accordingly, this species is herein reassigned to the monobathrid camerate crinoid family Paramelocrinidae.

Pandorinellina? boucoti (Klapper) is based on material from the Lochkovian–Pragian (Devonian) section at Royal Creek, Yukon Territory, Canada, where it is found with species of the pesavis and sulcatus Zones. The species is also a rare element in the late Lochkovian–early Pragian faunas in the Toquima Range, central Nevada, where it is found within the same zones. Pandorinellina? boucoti has been recovered from 17 beds in sequence at the IK IV section in the McMonnigal Limestone and shows a morphologic change from a Pa element with a simple blade, small lateral lobes, and an enlarged triangular anterior denticle to a Pa element with ornamented pillars surmounting both platform lobes. The simple blade form is present in beds IK IV 21–16. The next overlying bed yields specimens with a single pillar-like enlargement of the larger platform lobe and a slight swelling on the smaller platform lobe. The following beds (IK IV 14–6) have only morphotypes with the pillar-like enlargement on both platform lobes.

This morphologic change effectively divides the upper pesavis Zone into two segments in the IK IV section. The rarity of this species, however, will probably limit the usefulness of the lineage in refined biostratigraphy and the sequence of morphotypes needs to be verified in other areas. Nevertheless, where present, P.? boucoti should improve the accuracy of correlation in the late Lochkovian and early Pragian.

New and old species and genera of the family Guadalupiidae (spherulitic hypercalcified demosponges of the order Agelasida) are described or redescribed from the West Texas Permian. The entire family is reviewed and observations are made on the epibionts, growth patterns, functional morphology, ecological relationships, morphologic variability, modular structure, and evolutionary history of these largely reef-dwelling sponges. The stratigraphic distribution of species is also noted; many are limited and can define zones. The new genera Exovasa and Incisimura and the new species Guadalupia auricula, G. cupulosa, G. ramescens, G. microcamera, G. vasa, Cystothalamia megacysta, Lemonea simplex, Incisimura bella, and Exovasa cystauletoides are described. Almost all previously published taxa are redescribed and in some cases redefined. The Guadalupiidae are unique among hypercalcified sponges in having a modular thalamid layer (thalamidarium) covered on the exhalant surface by a non-modular stromatoporoid-like layer (trabecularium).

Triangulotarbus terrehautensis n. gen. and sp. is a Pennsylvanian phalangiotarbid (Arachnida) that occurs in the sandy shales of the lower Shelburn Formation, McLeansboro Group, Desmoinesian Series, above Coal VII (Danville Coal) of the Dugger Formation. Triangulotarbus terrehautensis is the youngest phalangiotarbid that has been collected in North America.

Three new species of the shallow-marine, warm-water bivalve Plicatula are reported from the upper Paleocene Santa Susana Formation of southern California. Plicatula simiensis new species is from the middle part of the formation on the south side of Simi Valley and occurs as a displaced specimen in deep-marine turbidites. Plicatula lapidicina new species and P. trailerensis new species are both from coralline-algal-rich muddy siltstone just beneath a nearshore, coralline-algal limestone interval in the upper part of the formation in the Santa Ynez Canyon area, east-central Santa Monica Mountains. These three new species represent the first late Paleocene records of genus Plicatula on the west coast of North America and the first Paleocene records of this genus in southern California.

With differentiated tissues and organs, a high-level eukaryotic macroalga Lanceaphyton xiaojiangensis n. gen. n. sp. lived on the middle–late Ediacaran (ca. 560–551 Ma) seafloor in South China. Its body had a pith (perhaps mechanical tissue) and outer tissue (perhaps epidermis and/or cortex). The lance-like macroalga consists of an unbranching thallus that grew over the sediment surface for sunlight and a holdfast grown into sediments to keep the thallus fixed on the seafloor. The pithy stipe (lower thallus) might have served to support the upper pithless thallus for photosynthesis. The holdfast is composed of a tapering pithy rhizome growing down into the sediments, with many filamentous pithless rhizoids dispersedly growing within the sediments. With the differentiated tissues and organs, especially the pith accounting for about half of the width of the rhizome and stipe, Lanceaphyton n. gen. was a high-level eukaryotic macroalga, similar to phaeophytes in morphological features, but further research is needed on its microstructural details. The pithy macroalga shows that the macroalgal pith had emerged in the Ediacaran.

UUID: http://zoobank.org/bc924c5c-84e4-4170-9ca1-caee0d56c6d5.

Gastropods are rare fossils in the Cambrian of Wisconsin. They are usually small and flattened. During the summer of 1978, while collecting trilobites along the western side of the state, I discovered a new gastropod in the Crepicephalus zone (as defined by Twenhofel, Raasch, and Thwaites, 1935; Nelson, 1951). It is a three-dimensional fossil represented by external mold and steinkern. This was the only gastropod uncovered during the splitting of over 200 kilograms of sandstone, which also yielded hundreds of trilobite cranidia and pygidia.

Gordonaster brassfieldensis is a new genus and species of Asteroidea (Echinodermata) described from the Lower Silurian Brassfield Formation of east-central Kentucky. Tentatively assigned to the poorly understood Palaeasteridae, Gordonaster shares much with Ordovician asteroids, yet it also exhibits apparent homoplasies that presage the post-Paleozoic crown group. Available specimens also indicate that the ontogenetic pattern of ossicular addition seen in the crown group was established during the Paleozoic.

The discovery of a new species, Cyclolampas altus new species in the upper Callovian of Burgundy (France) leads to the systematic revision of the rare echinoid genus Cyclolampas Pomel, 1883. Two morphometric approaches are used jointly to describe and quantify variations in test shape: the analysis of linear measurements and the Elliptic Fourier shape analysis. Both analyses yield congruent results that highlight the amplitude of within-species variations and quantify the part due to allometry. Along with the description of C. altus, the systematic position of species formerly assigned to the genera Pygorhytis Pomel, 1883 and Cyclolampas is amended. Previously attributed to the genus Pygorhytis, Cyclolampas castanea (Desor, 1858) is reassigned to the genus Cyclolampas on the base of new observations. Conversely, the examination of the Bajocian species Pygorhytis kiliani (Lambert, 1909) and Pygorhytis gillieroni Desor in Desor and de Loriol, 1872, which were previously assigned to Cyclolampas now supports their taxonomic reassignment to the genus Pygorhytis. Finally, the two species Cyclolampas verneuili (Cotteau, 1870) and Cyclolampas cotteaui Mintz, 1966 (nomen nudum) are considered junior synonyms of the genus type species Cyclolampas voltzii (Agassiz, 1839). The questioned origin date of the genus, estimated either to the Bajocian or to the Oxfordian, is now clearly established to be upper Callovian. These new results fit well with the overall scheme of atelostomate echinoid evolution and migration to deep-sea environments during the Middle and Upper Jurassic.

Murthya, a new ostracode genus of Cytherinae, is proposed for the species previously described as Leptocythere chadopadiensis Lyubimova and Guha from the Lower Miocene beds of Kachchh District, India. The genus also occurs in the Lower Miocene beds of Saurashtra, Quilon, and Thanjavur.

Agetolites is a problematic Late Ordovician genus possessing traits of both tabulate and rugose corals. The presence of numerous mural pores has often been considered to indicate a relation to tabulates, although an affinity to rugosans has also been proposed, based mainly on well-developed septa that alternate in length. To further consider the taxonomic position of Agetolites, growth characteristics of coralla representing three species from the Xiazhen Formation in South China are documented and assessed, focusing on modes of corallite increase. Three major modes of increase are recognized. By far the most common mode involves the development of an offset from a connective mural pore, without a clear relationship to a particular parent corallite. This mode of increase is usually associated with corner pores, but in one case occurs at a wall pore. The lateral mode of increase, which is relatively uncommon, is a typical feature in corallites along the boundary of intergrowths with stromatoporoids. The axial mode of increase is rare, occurring during rejuvenation of a damaged corallite or during regeneration following termination of a corallite. The mode of corallite increase that is characteristic of Agetolites, involving a connective mural pore and occurring without evidence of a particular parent, supports the interpretation that this genus is not a rugosan or a typical favositid tabulate. Mural pores are unknown in rugosans, and offsets arise from distinct parent corallites in favositids. The Ordovician genus Lichenaria, considered a representative of the most primitive stock of tabulate corals, shows the closest similarities with types of increase in Agetolites. Certain aspects of lateral and axial increase in Agetolites are comparable to features in a few more genera of Ordovician tabulates, further supporting a tabulate affinity. The phylogenetic relation of Agetolites to those and other tabulate genera, however, remains unresolved.

West Falls Group strata (Chemung facies) of Upper Devonian (Frasnian) age in New York State reflect sedimentation on a storm dominated sandy shelf. Rugose corals occur in storm deposited coquinites rich in bioclastic debris and are abundant locally, although representing only three species, Tabulophyllum orientale (Stumm), Macgeea ponderosa Stumm, and Disphyllum caespitosum (Goldfuss). The Tabulophyllum and Macgeea species are both characterized by large amounts of stereome (biogenic calcite) in the apical part of the corallite, perhaps useful in stabilizing corallites in the sediment.