The crinoid column is a paradox of crinoid paleontology. The crown is required for taxonomic identification and, therefore, prerequisite for phylogenetic, paleoecologic, or other studies. However, column elements (columnals and pluricolumnals) are by far the most common crinoidal fossil remains. The biostratigraphic utility of crinoid columns has been demonstrated in some cases (e.g., Donovan, 1984), but this is done with the risk of developing a parataxonomy among crinoids because in most cases columnals are not associated with crowns and, therefore, cannot be assigned to crown species with certainty.

Rosette-shaped problematica are relatively common structures in the Phanerozoic rock record. Historically, they have been accorded a variety of names and documented from various shallow to deep marine environments. Unfortunately, the detailed interpretation of many such structures as biogenic (trace fossils, medusoids, or other body fossils; see, for example, Häntzschel, 1970, 1975) or nonbiogenic (for example, Pickerill and Harris, 1979) in origin still remains to be resolved. However, a detailed analysis of one such structure by Fürsich and Bromley (1985), namely Dactyloidites Hall, 1886, convincingly demonstrated its biogenic origin. The distinctive morphology of Dactyloidites and its synonyms was interpreted by Fürsich and Bromley (1985) to result from successive probings of an essentially stationary deposit-feeding, worm-like organism, possibly possessing a proboscis, to produce a rosetted, vertical spreiten with a centrally located, vertical or subvertical shaft.

Several specimens of biogenic structures somewhat resembling plug-shaped ichnofossils have been collected in two muddy deposits, Sicilian (Early Pleistocene) in age (Bossio et al., 1987), outcropping near Lecce, southern Apulia, Italy. One sequence is exposed in an unused quarry located at the eastern side of the Cutrofiano–Supersano road, 31 km post; the other one is in an active quarry, southwest of Lecce, near the village of San Pietro in Lama (Figure 1). The diagnostic features of the traces differ from those of the five ichnogenera recognized by Pemberton et al. (1988) for plug-shaped ichnofossils. The minor ichnogenera related to plug-shaped trace fossils, as indicated by those authors, are also different from the present structure. A new ichnogenus is proposed to cover this form.

The fossil brachiopods of the Caribbean region are reasonably well known following publication of Cooper's (1979) monograph; however, the Jamaican fauna was not considered in this volume. Until recently, only Trechmann (1927, 1930) had described and figured fossil brachiopods from the island. Harper (1993; Harper and Donovan, 1990) has recently revised Trechmann's identifications and added to the still small faunal list, which includes two Cretaceous and 11 Cenozoic species (excluding those discussed below). Further specimens continue to be found and the present communication is a description of a significant collection of small terebratellaceans from the top of the Paleocene to Eocene Richmond Formation of eastern Jamaica. One of the two species described herein was originally recognized on the basis of three brachial valves as Argyrotheca sp. 1 in Harper (1993). The availability of superior material has confirmed the uniqueness of this species and has permitted adequate description and diagnosis. All specimens described herein are deposited in the James Mitchell Museum of University College, Galway (JMM), and the British Museum (Natural History), London (BMNH).

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.

Numerous specimens of the neritid gastropod Nerita (Bajanerita) n. subgen. californiensis (White, 1885) are present in the Upper Cretaceous Rosario Formation at Punta Banda, Baja California, Mexico (Figure 1). Marincovich (1975) assigned these strata to a Late Campanian to Early Maastrichtian age. The strata contain extensive biostromal deposits of the caprinid rudistid bivalve Coralliochama orcutti White, 1885, that probably lived below mean wave base in a shallow-water, low-energy environment periodically affected by storm waves or currents (Marincovich, 1975). The nearby shoreline was apparently defined by steep wave-washed bedrock cliffs and local pocket beaches that formed along the margin of a forearc basin (Yeo, 1984). Scattered about in the sandstone matrix among the rudistid remains are the small-sized specimens of N. (B.) californiensis, which commonly weather out as resistant, complete shells on the surface of the rock. Saul (1970) concluded that the neritid and other shallow-water gastropods at Punta Banda accumulated in sediment-trapping depressions within the Coralliochama buildups. These gastropods had originally roamed over the algal pastures of these buildups. The color patterns preserved on many of the specimens of N. (B.) californiensis also provide evidence that the depth of water was shallow and within the photic zone. Furthermore, Sohl (1971) reported that Campanian and Maastrichtian gastropod assemblages of the Baja California region are mostly associated with rudist buildups, and warm-water rocky intertidal neritids are among the dominant faunal elements. Lowenstam and Epstein (1959), using oxygen-isotope studies of an ammonite, suggested that the Punta Banda rudistids lived at a marginally tropical temperature of about 19°C.

In 1904 Osborn named a new species of Mesohippus, M. validus, based on a specimen consisting of a skull, jaws, and portions of the limbs. Osborn identified this specimen as American Museum of Natural History (AMNH) catalog number 680 and provided a brief description, some measurements, and an illustration.

Upper Silurian and lowermost Devonian fossil plant assemblages are often dominated by fragmentary remains of problematic land plants that are composed of a tubular anatomy. Traditionally, these remains have been divided into two morphotypes: large three-dimensionally preserved axes (the Prototaxites group), and smaller thalloid incrustations referred to the genus Nematothallus Lang. Because of their peculiar anatomy of different combinations of tubular elements, these plants do not appear to be closely related to the Tracheidatae (sensu Bremer et al., 1987). Neither do they fit easily into any extant algal groups (Rossat, 1952; Edwards, 1982; Strother, 1988). For these reasons, when he first described the genus Nematothallus, Lang (1937) constructed an informal class of plants, the nematophytales, to include these fossils. Strother (1988) further emphasized the differences between the nematophytales and both embryophytes and algae by placing them into a new group, the Paraphyta.