The proboscidean Gomphotherium is reported here from the Alajuela Formation of Panama. Gomphotherium was widespread throughout Holarctica during the Miocene, and the Panama fossil represents the extreme southernmost occurrence of this genus in the New World. Allocation of the Panama Gomphotherium to a valid species is impossible given both the fragmentary material represented and the taxonomic complexity of species assigned to this genus. In North America, Gomphotherium has a relatively long biochronological range from the middle Miocene (~15 Ma) to early Pliocene (~5 Ma). Based on morphological comparisons, the Panama Gomphotherium is either middle Miocene, thus representing the earliest-known entry of this genus into Central America, or late Miocene/early Pliocene, which challenges the currently accepted middle Miocene age of the Alajuela Formation as it has been previously reported from Panama.

A rare diminutive belemnite, Pumiliobelus n. gen., is described based on the new species P. haigi and P. tumidus from the upper Gearle Siltstone (Cenomanian) of the Carnarvon Basin, Western Australia. No smaller belemnites than these species are known. That they are based on adult specimens rather than juveniles is supported by a large sample, some 80 specimens, of P. haigi which collectively show a proportional range in size typical of belemnite species in general, a group in which juveniles are conspicuously lacking in the fossil record. Rostral morphology places Pumiliobelus in the Dimitobelidae, a distinctively Austral family of Aptian–Maastrichtian age, which became progressively restricted to high latitudes through the late Cretaceous. Each species of Pumiliobelus is known from a single locality where it co-occurs with the long-ranging (Albian–Cenomanian) Dimitobelus diptychus Whitehouse of widespread distribution at mid to high latitudes in the Southern Hemisphere. Dwarfism in the Dimitobelidae, as expressed by Pumiliobelus, is considered to reflect adaptive evolution to engage opportunistic life strategies that favored small body size and rapid population turnover. The rare occurrence of dwarf Dimitobelidae indicates that such strategies were limited in both geographic range and duration. Dwarfism expressed by Pumiliobelus may relate to paedomorphosis induced by rising seawater temperatures in the mid Cretaceous.

A new crinoid association reported from the Kope Formation (Katian, Ordovician) of northern Kentucky and southwestern Ohio changes the model for facies distribution of crinoids along an Ordovician onshore-offshore depth gradient. Glyptocrinus nodosus n. sp., Plicodendrocrinus casei (Meek, 1871), Cincinnaticrinus varibrachialis (Warn and Strimple, 1977), and Ectenocrinus simplex (Hall, 1847) are reported from a suspension-feeding assemblage with 26 taxa. This assemblage developed above an argillaceous packstone with most of the fossils preserved in shale. The fauna was comprised principally of secondary epifaunally tiered suspension feeders, deposit feeders, and predators. This is the first reported occurrence of Glyptocrinus Hall, 1847 and Plicodendrocrinus Brower, 1995 from the Kope Formation (lower Cincinnatian), and Glyptocrinus is represented by a new species, G. nodosus. Also, this is the first report of pinnulate camerate crinoids from the deep-water facies of the Kope Formation. Thus, deep-water Cincinnatian crinoid assemblages were comprised of disparids, cladids, and camerates; and the assemblage was characterized by a variety of filtration fan types for acquisition of resources.

Llanocystis wilbernsensis n. gen. n. sp. (Eocrinoidea, Echinodermata) is described based on three specimens from the Furongian Point Peak Shale Member of the Wilberns Formation in central Texas. It displays a unique morphology including a very long stem constructed with holomeric columnals, few feeding appendages, and a polyplated theca. The specimens occur in an intraformational conglomerate deposited in a proximal carbonate platform environment and represent an example of the poorly documented “pelmatozoan” radiation that occurred in proximal facies by the end of the Cambrian.

The Cretaceous Period (145–66 Ma) consisted of several oceanic anoxic events (120–80 Ma), stimulated by global greenhouse effects. The Oceanic Anoxic Event 2 (OAE2) occurred worldwide from the late Cenomanian to the early-middle Turonian, causing a significant faunal turnover, mostly in marine biota, pushing some species to the brink of extinction. Some organisms also underwent morphological changes, including reduction in size. This anoxic event drove other changes—e.g., in habitats or strategy of life. We show that stalkless crinoids (comatulids) from the Turonian of Poland adapted to unfavorable environmental conditions by reducing their body size. Furthermore, at the moment when environmental factors became favorable again, these crinoids regained their regular (pre-event) size. This phenomenon likely illustrates the so-called dwarfing mode of the Lilliput effect.

A new eocrinoid ?Ubaghsicystis sp. from the middle Cambrian (Series 3, Stage 5) Burgess Shale is reported based on a single known specimen. This species extends the stratigraphic range of columnal-bearing eocrinoids in Laurentia significantly from Cambrian Stage 7 (Guzhangian) to Stage 5. It increases the diversity of echinoderms in this well-known fossil-Lagerstätte, provides the oldest evidence of columnal-bearing eocrinoids from Laurentia, and further documents the cosmopolitan distribution of middle Cambrian echinoderm clades.

A tooth recovered from the middle Miocene Choptank Formation (Chesapeake Group) of Maryland is identified as a new cynarctin borophagine (Canidae: Borophaginae: Cynarctina), here called Cynarctus wangi n. sp. The tooth, identified as a right upper second molar, represents the first carnivoran material reported from the Choptank Formation and part of a limited record of borophagine canids from eastern North America. As ?Cynarctus marylandica (Berry, 1938), another cynarctin borophagine from the older Calvert Formation, is known only from lower dentition, its generic affinities are uncertain. However, features of this new material are compared to features of ?C. marylandica through occlusal relationships, allowing for referral to a distinct species. Even so, the Choptank Formation material still offers two possible scenarios regarding its identification. In one, its geographic and stratigraphic provenance could imply that it belongs to ?C. marylandica. If this were correct, then the generic placement of ?C. marylandica would be correct and the taxon would be more derived than some other Cynarctus species in regard to hypocarnivory, and less derived than others. The second possibility, and the one believed to be most probable, is that a distinct cynarctin borophagine is present in the Chesapeake Group in strata younger than the type specimen of ?C. marylandica. This new borophagine canid expands the sparse fossil record of this group in northeastern North America and furthers our knowledge of the fossil record of terrestrial taxa in this region.