Fossil raninid crabs, Cretacoranina punctata (Rathbun, 1935), from the Pawpaw Formation (Upper Cretaceous) of Fort Worth, Texas, exhibit an unusual cuticular morphology. Comparison of the cuticle of extant Raninoides louisianensis to that of C. punctata reveals general similarities in endocuticular, exocuticular, and epicuticular ultrastructure; however, their gross morphology is strikingly different. The surface of the carapace of C. punctata appears pebbled, much like the surface of a basketball, with closely packed, hexagonal caps. In cross-section, these caps are the upper portion of fungiform structures within convoluted exocuticle. Along the anterior margin, anterolateral margins, and pterygostomial region of the carapace of C. punctata each cap dips slightly posteriorly, creating a series of tiny terraces. In contrast to terrace lines, questa lines, spines, and nodes that provide frictional resistance in interactions with coarse-grained sediments, the fine relief and contouring of the pebbled surface of the carapace of C. punctata provides frictional resistance in interactions with fine-grained sediments. Cretacoranina dichrous, C. trechmanni, C. testacea, and C. schloenbachi, as well as Eucorystes carteri were all found to possess variations of the exocuticular structures seen on C. punctata. This pebbled surface has not been recognized in any other decapod taxon, nor has its structure and function been described previously.

Specimens of Peronopora Nicholson, 1881, are abundant in Upper Ordovician rocks of the North American Midcontinent. Based on the positions of units in the Composite Conodont Standard Section, we have sampled 211 specimens over a stratigraphic interval of 9.1 million years. The average duration of sample spacing is 61,664 years but is commonly as small as 32,800 yr.

Thirty-four morphometric characters were measured in each specimen and were converted into multistate characters; character-state breaks were established based upon each character's ability to discriminate between phenetic groupings. Each character was subsequently weighted based on the number of derived states, degree of independence from other attributes, and estimated heritability.

Cladistic analysis of these data indicate that there are eight species in Peronopora each consisting of an optimally defined crown group and a basal stem group (or paraclade). Character states shared by stem and crown groups define species but, within species, stem and crown groups also differ in some character states. The species are, in ascending order from the base of the tree, Peronopora decipiens (Rominger, 1886), P. compressa (Ulrich, 1979), P. pauca Utgaard and Perry, 1964, P. milleri Nickles, 1905, P. horowitzi new species, P. vera Ulrich, 1888, P. sparsa Brown and Daly, 1985, and finally P. dubia (Cumings and Galloway, 1913). Diagnostic keys permit the unique assignment of each specimen to a species and the separation of members of stem groups from those of crown groups. Thirty-one characters are required to discriminate between all 211 specimens. This contrasts with previous studies of Peronopora where eight or fewer characteristics were used. Of the ten characters most useful in discrimination, only three had been used in the conventional species literature. This accounts, largely, for only 29.8 percent (51 of 171) of previously identified specimens being classified as members of the same species in this analysis. Discriminant function analysis of original measurements, using species identity as the grouping criterion, produces statistically significant separation of species.

It appears that stratigraphic position had an explicit and undue effect on previous concepts of species many of which could not be recognized independently of stratigraphic position. All species of Peronopora appear, or are inferred to have appeared, within the Lexington Limestone between the base of the Grier Member and the top of the Millersburg Member. The cladogram indicates that species evolved in a sequential order, but their first appearance datums have been stratigraphically punctuated. Three species have ranges terminating in the Early to Middle Maysvillian, one in the Middle Richmondian, and four in the Late Richmondian. The latter four (or five) of these species died out in the extinction associated with the unconformity at the top of the Richmondian.

Aetosaur fossils from the Upper Triassic Ischigualasto Formation of Argentina formerly assigned to Aetosauroides scagliai Casamiquela and Argentinosuchus bonapartei Casamiquela are reassigned to Stagonolepis robertsoni Agassiz (small specimens) and S. wellesi (Long and Ballew) (larger specimens). Numerous features of the skull, vertebral column, appendicular skeleton, and particularly the armor, of these Argentinian aetosaurs are identical to those of Stagonolepis and differ from other aetosaurs. Identification of Stagonolepis in South America has important implications for the correlation of nonmarine strata across Late Triassic Pangea. Stagonolepis is an index taxon of the Adamanian land-vertebrate faunachron of latest Carnian age. Its occurrences in the Ischigualasto and Santa Maria formations, as well as at the type locality in the Lossiemouth Sandstone of Scotland and in the Blasensandstein of the German Keuper, cross-correlate with a well-established tetrapod biostratigraphy of the Chinle Group in western North America. Thus, all Stagonolepis records are of Adamanian (latest Carnian) age, not Otischalkian (early or “middle” Carnian) age, as proposed by some earlier workers. This correlation also demonstrates that the oldest known dinosaurs are not from the Ischigualasto and Santa Maria formations. Previous workers obtained radioisotopic dates of 227.8 Ma from the Ischigualasto Formation, providing a maximum numerical date for Stagonolepis-bearing units. This date must be late Carnian, not of Ladinian age, and thus supports the apparent age of the Ladinian-Carnian boundary (232 Ma) of time scales based on the Newark Supergroup in eastern North America.

Codellaster keepersae new genus and species, from the Upper Cretaceous Codell Sandstone Member of the Carlile Shale of Colorado (U.S.A.), is assigned to the asteroid (Echinodermata) family Goniasteridae. Although clearly a goniasterid, the flattened body form and details of morphology of C. keepersae are remarkably similar to corresponding features of the modern astropectinid Astropecten regalis and also of the luidiid Luidia (Platasterias) latiradiata. The discovery facies of C. keepersae includes low-angle crossbeds and asymmetrical ripple marks that are suggestive of a very shallow marine environment. Both the modern species occur in shallow, turbulent settings, and homeomorphy beween ancient and modern asteroids suggests similar selective pressures and evolutionary responses. Limited evidence suggests goniasterids might have been more common in shallower waters during the Cretaceous than they are today, and absence of modern Codellaster-like goniasterids indicates that the family abandoned these habitats, although the fundamental morphological response to such settings remained viable for asteroid organization.

Lake deposits of the Pagoda Formation (Upper Carboniferous?-Lower Permian) at Mt. Butters, Shackleton Glacier area, central Transantarctic Mountains, Antarctica, yield a low diversity biota including a new species of conchostracan, Cyzicus (Lioestheria) shackletonensis. Locally, conchostracans occur in large numbers near the tops of thin coarsening-upward cycles in siliciclastic sediments. Regionally, the Pagoda Formation consists of glacigenic deposits of the Gondwanide ice sheet that covered much of the land in southern high latitudes. At Mt. Butters, the lake deposits document the presence of an ice-margin lake in front of the advancing ice sheet. Deposition from suspension within the lake was interrupted by introduction of sand and silt deposited in the conchostracan-bearing, upward-coarsening sequences. Conchostracans of the Pagoda Formation are associated with other arthropods (euthycarcinoids and ostracodes), and wood fragments; burrows produced by small animals moving just beneath the sediment surface are abundant in some horizons. Few conchostracan occurrences are known from the Carboniferous-Permian of Antarctica; this is the second recorded occurrence, and it increases the number of described species to three.

Rare to abundant silicified polyplacophoran faunas occur in the late Wolfcampian Bird Spring Formation and the Leonardian Pequop and Loray Formations in Nevada, the Leonardian Arcturus Formation in Utah, and the early Leonardian Ft. Apache Limestone Member of the Supai Formation in Arizona. The faunas associated with the polyplacophorans are dominated by molluscs. New species include Gryphochiton distinctus, Acutichiton gracilis, A. nevadensis, and Arcochiton richardsoni. Traces of color patterns are present on Arcochiton richardsoni.

Two neogastropod species occur in brackish intervals in the Pebas Formation (late Middle to early Late Miocene) of Peru and Colombia in western Amazonia. Purpura woodwardi Roxo, 1924, is assigned to Melongena Schumacher, 1817 (Melongenidae), and ?Nassarius reductus (Nassariidae) is recognized as a new species. These gastropods are among the very few marine invaders in the otherwise freshwater Pebas fauna. The small number of marine to freshwater transitions among South American molluscs contrasts with the situation among South American fishes and southeast Asian molluscs. It may be related to seasonal fluctuations in water level and anoxia in present-day South American freshwater environments, as well as to predation and productivity.

Costistricklandia is a common, easily recognizable pentamerid brachiopod in upper Llandovery to lowest Wenlock rocks of eastern Laurentia, Avalonia and Baltica. In this paper, the poorly known Costistricklandia canadensis (Billings) is re-described from the upper Telychian Rockway Dolomite of the Niagara Escarpment, Ontario. Compared to the relatively complete record of the Stricklandia-Costistricklandia evolution in the Welsh Borderland and the Baltic region, true representatives of the Stricklandia lens lineage are sporadic in North America, including those from the Merrimack Formation of Anticosti Island, the Red Mountain Formation of Alabama, the Hopkinton Formation of Iowa, and the Nonda Formation of the northern Rocky Mountains. Although the exact mode of speciation in the Stricklandia-Costistricklandia and the Pentamerus-Pentameroides transitions remains debatable, the common association of Costistricklandia and Pentameroides make them a useful concurrent biozone for correlating middle to upper Telychian rocks of North America and Europe. Paleobiogeographically, the Pentameroides-Costistricklandia Fauna marks the third major pulse of pentamerid faunal migration between Laurentia and its adjacent paleo-plates during the Early Silurian, following the limited intercontinental dispersal of the early Llandovery Virgiana Fauna and the quasi-cosmopolitan dispersal of the middle Llandovery Pentamerus Fauna.

Re-examination of the dentitions of carpolestid plesiadapiform mammals from the late Paleocene Swan Hills locality, northern Alberta, and correlative localities in the vicinity of Roche Percée, southeastern Saskatchewan, Canada, indicates that Carpodaptes cygneus (Russell) as known from these sites is polyphyletic: the name C. cygneus is here restricted to the Swan Hills carpolestid, while the Roche Percée form represents a new, more derived species, Carpodaptes stonleyi. Other purported records of C. cygneus are reconsidered as well: C. cygneus from DW-1, central Alberta, is more appropriately dubbed C. cf. cygneus; C. cygneus at Canyon Ski Quarry, central Alberta, is best identified as C. cf. stonleyi, while C. cf. cygneus from Police Point, southeastern Alberta, has closest affinities to C. hazelae Simpson. Carpolestids from the Tongue River Formation, North Dakota, are referred to Carpodaptes cf. hobackensis Dorr and C. cf. hazelae. After a review of the available evidence, the recent hypothesis that C. cygneus and other North American carpolestids are congeneric with Carpocristes oriens Beard and Wang from the Paleocene or Eocene of China, is rejected.

One new genus, Kalops, and two new species, K. monophrys and K. diophrys, are described from the Carboniferous (Namurian) marine Bear Gulch limestone of Montana (USA). The most conspicuous features of these elongate fusiform actinopterygians consist of one or two rows of anamestic supraorbital bones, a mosaic of suborbitals, and the presence of two rows of extrascapulars in one species. Discussions of their anatomical, morphometrical, and growth characters result in their placement in the same genus. Comparisons with other Palaeozoic actinopterygians show that Kalops is a Palaeoniscimorpha (=basal Actinopteri sensu Patterson).

Numerous pygocephalomorph crustaceans occur with conchostracans, plants, fishes, amphibians, and amniotes in the Petrolia Formation (Leonardian Series, Lower Permian) of Baylor and Archer counties, Texas. Two pygocephalomorph species are represented; Mamayocaris serendipitous, new species, by hundreds of specimens that appear to be molted exoskeletons, and Paulocaris schrami, new species, by only a few specimens. Mamayocaris has been reported previously from the Lower Permian of Texas and South Dakota and the Upper Carboniferous of Illinois; Paulocaris was previously known only from South America. Associated plant assemblages are dominated by conifers accompanied by other Early Permian and some Late Carboniferous elements. Accompanying vertebrate remains include aquatic to fully terrestrial forms with close taxonomic ties to genera or families recorded in Upper Carboniferous deposits. The fossils are preserved in local deposits of thin (<2 cm), lenticular to nodular beds of limestone and thin (<15 cm) intervals of dark-gray claystone. These deposits accumulated in abandoned, standing-water segments of suspended-load fluvial channels. The archaic nature of these plant and animal assemblages supports previous interpretations that the Permian Petrolia Formation contains paleoenvironmentally isolated biotic elements characteristic of the Carboniferous and underscores prior depictions of the assemblages as relictual.

Kochaspids are an informal group of ptychopariid trilobites that were both abundant and widespread in the early Middle Cambrian of North America. Based on the reassociation of pygidia and cranidia of some kochaspids, Kochiella Poulsen, 1927, is redefined and Hadrocephalites n. gen. is proposed. Hadrocephalites includes taxa previously assigned by Rasetti and Palmer to Schistometopus Resser, 1938a. Schistometopus is considered nomen dubium. Representatives of Kochiella and Hadrocephalites from the Pioche Shale and Carrara Formation of Nevada are described, including the new species Kochiella rasettii, K. brevaspis, Hadrocephalites lyndonensis, and H. rhytidodes. Other kochaspids previously assigned to Kochaspis Resser, 1935; Eiffelaspis Chang, 1963; Schistometopus; and Kochiella are discussed and some are reassigned. The type specimens of Kochiella augusta (Walcott, 1886); K. crito (Walcott, 1917b); K. chares (Walcott, 1917a); K. mansfieldi Resser, 1939; K. arenosa Resser, 1939; Hadrocephalites carina (Walcott, 1917b), and H. cecinna (Walcott, 1917b) are re-illustrated.

In cyclical Pennsylvanian strata, conodonts find their greatest stratigraphic utility as biotic signatures of physically defined stratigraphic entities (cycles, parasequences, high frequency sequences, etc.) rather then the primary means of stratigraphic subdivision (e.g., biostratigraphic interval zones). The practice of identifying depositional entities for purposes of regional correlation on the basis of their constituent conodont faunas is herein called conodont sequence biostratigraphy. In this paper, the concept is utilized to successfully correlate Pennsylvanian cycles of the Paradox basin with their Midcontinent counterparts.

The Honaker Trail section is the most accessible and well-studied succession of carbonate shelf strata in the Paradox basin. Approximately 350 m of cyclically bedded limestone, sandstone, and shale comprising 53 fifth-order cycles are exposed along the cliffs of the deeply entrenched San Juan River. Maximum transgressive facies of 19 cycles yielded Idiognathodus-Neognathodus- and/or Streptognathodus-dominated conodont faunas. Those from the Chimney Rock, Gothic, LHT-5, UHT-3, UHT-5, UHT-8, unnamed limestone, and Shafer correspond to faunas from the Verdigris, Lower Fort Scott, Altamont (Lake Neosho), Lost Branch, Hertha (Mound City), Swope (Hushpuckney), Dennis (Stark), and South Bend cycles of the Midcontinent, respectively. By extrapolation, all minor cycles of the Marmaton, Pleasanton, and Bronson Groups (except for the Critzer) also appear to have counterparts at Honaker Trail.

The position of the Desmoinesian–Missourian boundary in the Honaker Trail section can be approximated using conodonts in conjunction with fusulinids. The highest Desmoinesian conodont fauna, the Idiognathodus nodocarinatus fauna, occurs in cycle UHT-3 in the lower part of the Upper Honaker Trail sequence. The highest occurrence of Beedeina occurs in the same cycle. The lowest conodont fauna with the Missourian species I. eccentricus appears two cycles higher, in cycle UHT-5. Because in the Midcontinent region a small interval of strata separates the first appearance of I. eccentricus from the base of the Missourian, we place the base of the Missourian at the base of cycle UHT-4 (bed 105) at Honaker Trail. The appearance of Streptognathodus firmus and S. pawhuskaensis in the Shafer limestone indicates that the Missourian–Virgilian boundary lies slightly above or below this stratigraphic horizon.

The ichnogenus Pholeus Fiege, 1944, is a common constituent of the Lower Muschelkalk (Middle Triassic) carbonates of the Germanic Basin, where it occurs in the upper part of shallowing upward cycles. It is restricted to a marly limestone lithofacies and is commonly associated with omission and erosion surfaces. The dwelling structures (domichnia) were created in a shallow-marine to lagoonal paleoenvironment in an intertidal to shallow subtidal setting. New material from Thuringia and Lower Saxony makes a reevaluation of Pholeus possible and confirms the validity of this ichnogenus. Certain features, such as general form, wall, lining, and branching differentiate it from similar trace fossils. In addition to the already described P. abomasoformis, three new ichnospecies are named for distinctive forms: P. bifurcatus, P. platiformis, and P. elongatus. Based on geometry, size, and wall lining, the burrow producers were most probably decapod crustaceans. Many similarities to modern burrows of Callianassa sp., Neocallichirus grandimina, and Nephrops norvegicus suggest thalassinian shrimps and lobsters as likely tracemakers of Pholeus burrows. Compound burrow systems and retrusive burrow parts with spreiten-like structures are common and point to an upward shifting of the burrows related to certain sediment input in relation to tidal currents.

Brachiopods are common in the lower part of the late Early to Middle Devonian Bird Fiord Formation that is a carbonate-clastic transition succession found in Arctic Canada. These brachiopods, which lived in a shallow, near-shore, marine environment, includes three new genera: Borealistrophia, Arcticastrophia, and Grinnellathyis. The strophomenid Borealistrophia, which is characterized by two pairs of straight side septa, prominent and thick socket ridges, a thick but short median septum, and a cordate ventral muscle field, is found in the Baad Fiord, Blubber Point, and Norwegian members on Bathurst, Devon, North Kent, and Ellesmere islands. The strophomenid Arcticastrophia, which is distinctive because of its stout transmuscle septa, its narrow and low medium septum, and elevated ventral muscle field, is found in the Baad Fiord Member on Bathurst and Devon islands. The athyridid Grinnellathyris, which is characterized by an imperforated cardinal plate and inverted U-shaped jugum, is found in the Baad Fiord Member on Bathurst, North Kent, and Devon islands. The similarities between Grinnellathyris and Johnsonathyris Savage, Eberlein, and Churkin, 1978, in terms of their shell size and internal structures, may indicate that the latter evolved from the former.

The aïstopod family Phlegethontiidae is restudied based on new specimens from Pit 11 of Mazon Creek, Illinois, and the coal shales of Nýřany, Czech Republic, as well as most available specimens from North America. Phlegethontiids have highly fenestrate skulls, with orbits placed just anterior their skull's mid point. Dermal skull bones are greatly reduced in number and limited in extent, whereas the endochondral braincase is hyperossified. The frontals are fused medially and enclose the parietal foramen and anterior sagittal crest. As in most other aïstopods, the quadrate, pterygoid, and epipterygoid are fused into a composite bone, the palatoquadrate complex. Details of cranial anatomy contradict a previous model of cranial kinesis by severely limiting the skull's potential mobility. Remnants of the pectoral girdle are present, perhaps due to the presence of an operculum–opercularis-like connection to the stapes. No remnants of the pelvis are present.

Three species are recognised within the family. Phlegethontia linearis has short anterior vertebrae, high neural spines on at least the anterior four vertebrae, and vertebrae number between 230–250 in total. Phlegethontia longissima has low neural spines throughout the column, anterior vertebrae that are twice as long as P. linearis, and only 200–210 total vertebrae. Sillerpeton permianum, known from a single braincase and an unassociated string of vertebrae, is distinguished from Phlegethontia by the retention of a separate foramen for the passage of the occulomotor nerve. Phlegethontia “phanerhalpa” is a tiny braincase fragment that differs from the other species of Phlegethontia only in the placement of the jugular foramen relative to the centre of the foramen magnum. This is probably a size-related feature, and P. “phanerhalpa” is considered a nomen dubium.

Three important collections of European Devonian and Lower Carboniferous polyplacophorans have been located in United States institutions. The specimens provided a basis for better description of important characters and clarified some taxonomic assignments. Two new polyplacophoran species are in the collections, Helminthochiton carpenteri from the Devonian of Germany and Pterochiton absidatus from the Lower Carboniferous of Belgium. Beloplaxus sagittalis (Sandberger and Sandberger, 1853–1855) is recognized as a multiplacophoran and a new genus and species of turrilepadid, Bouturrilipas scutatus, is proposed.

Middle and Upper Devonian members of the phyllocarid order Archaeostraca Claus, 1888, are analyzed in both a phylogenetic and biogeographic context. Results of the phylogenetic analysis show that the suborders Ceratiocaridina Clarke in Zittel, 1900, and Rhinocaridina Hall and Clarke, 1888, are paraphyletic as traditionally defined. The diagnoses of these suborders are revised and the use of the suborders Echinocaridina Clarke in Zittel, 1900, and Pephricaridina Van Straelen, 1933, is proposed. Ceratiocaridina now contains the family Ceratiocarididae Salter, 1860; Rhinocaridina contains the family Rhinocarididae Hall and Clarke, 1888; Echinocaridina includes the families Aristozoidae Gürich, 1929, Ptychocarididae n. fam., and Echinocarididae Clarke in Zittel, 1900; Pephricaridina includes the families Pephricarididae Van Straelen, 1933, and Ohiocarididae Rolfe, 1962. Generic definitions within the Rhinocarididae, in particular “Rhinocaris” Clarke in Hall and Clarke, 1888, are revised. The genus Echinocaris is redefined to include a monophyletic assemblage of species. Each of these clades is supported by several synapomorphies. Two new genera, Paraechinocaris and Carinatacaris, are proposed. Biogeographic analysis of this group reveals an extremely low rate of vicariant speciation, while episodes of range expansion are frequent. All occurrences of vicariance preceded the Late Devonian mass extinction. This may suggest a relationship between increased dispersal, diminished speciation, and the Late Devonian biotic crisis. Parallels between the Late Devonian mass extinction and the modern biodiversity crisis are suggested by the frequency of episodes of range expansion indicative of invasive species.

Psilonichnus lutimuratus n. ichnosp. is described from a Pliocene estuarine-mouth depositional environment (Skolithos ichnofacies) of the Olympic Peninsula, Washington, U.S.A. These simple Y-, I-, and J-shaped, mud-lined burrows occur in situ as dense patches within alternating, wavy-bedded sandstone and mudstone in a storm and flood influenced coastal sequence from an active tectonic margin. The I- and J-shaped traces represent erosional modification of burrow tops during storm-flood events. The new ichnospecies differs from the two other Psilonichnus ichnospecies by the distinct mud-lining of the burrow wall. Comparison with living thalassinoidean shrimp burrows and shrimp ecology allow this new ichnospecies to be attributed to the extant mud shrimp Upogebia. Biological and behavioral characteristics of this living shrimp restrict it to the mouth of the open estuary, and these parameters can be used to narrowly define a shoreline environment in the stratigraphic record.

Evolutionary relationships between the Echinoconchidae, Productidae, Buxtoniinae, and Juresaniinae (Phylum Brachiopoda, Order Productida) have been the subject of debate for the better part of a century. The original (Muir-Wood and Williams, 1965) and revised (Brunton et al., 2000) Brachiopoda volumes of the Treatise on Invertebrate Paleontology use markedly different classifications and emphasize different characters. The 1965 Treatise classification for these taxa primarily was based on internal features, especially the cardinal process; the revised Treatise (2000) relied on external ornament and shell shape. Multiple phylogenetic analyses (global parsimony, stratocladistics, nearest-neighbor) of 14 genera, representing all of the relevant subfamilies and outgroups, are in strong agreement that 1) the subfamily Buxtoniinae belongs in the family Echinoconchidae, not to the Productidae; 2) the subfamily Juresaniinae is more closely related to the Echinoconchinae than to the Buxtoniinae; and 3) that internal characters, such as a shafted cardinal process and anterio-medial position of the brachial valve adductor field, provide the best phylogenetic signal, and are synapomorphic for the Echinoconchidae. Jackknifing and Bremer Support corroborate these results.