Postel Nunatak in the Patuxent Range has been previously mapped as Nelson Limestone but there was no biostratigraphic support for that interpretation until now. We confirm that limestone exposures at Postel Nunatak are at least partly correlated with the Nelson Limestone of the Neptune Range, 160 km north-east, and are not correlative with the lower Cambrian Schneider Hills Limestone of the Argentina Range. Upper beds have yielded the trilobites Suludella? davnii Palmer & Gatehouse, 1972 and Solenopleura pruina Palmer & Gatehouse, 1972, which provide a basis for assignment to Cambrian Series 3 (late middle Cambrian), within the Drumian or lower Guzhangian stages. Limestone beds were deposited in a shallow marine setting, ranging from supratidal to lagoonal facies with rare subtidal intervals. These settings contrast with deeper water facies of the Neptune Range. Despite limitations in sampling density, isotopic analysis indicates that a greater than +2.5‰ shift in δ13C is consistent with δ13C trends documented for the Drumian Stage. Because the upper and lower contacts at Postel Nunatak are covered by snow and ice, the relationship with rocks mapped as the Patuxent Formation in the Patuxent Range remains uncertain, but part of it may belong to the Precambrian Hannah Ridge Formation.

Latest Sandbian to early Katian sequences across Laurentia's epicontinental sea exhibit a transition from lithologies characterized as ‘warm-water’ carbonates to those characterized as ‘cool-water'carbonates. This shift occurs across the regionally recognized M4/M5 sequence stratigraphic boundary and has been attributed to climatic cooling and glaciation, basin reorganization and upwelling of open ocean water, and/or increased water turbidity and terrigenous input associated with the Taconic tectophase. Documentation of oxygen isotopic trends across the M4/M5 and through bracketing strata provides a potential means of distinguishing among these alternative scenarios; however, oxygen isotopic records generated to date have failed to settle the debate. This lack of resolution is because δ18O records are open to multiple interpretations and potentially confounding factors related to local environmental conditions have not been tested by examining the critical interval in multiple areas and different depositional settings. To begin to address this shortcoming, we present new species-specific and mixed assemblage conodont δ18O values in samples spanning the M4/M5 boundary from the Upper Mississippi Valley, Alabama, and Virginia. The new results are combined with previous studies, providing a record of δ18O variability across SE Laurentia. The combined dataset allows us to test for regional trends at a resolution not previously available. Our results document a ~1.5‰ decrease in values across Laurentia instead of increasing δ18O values across the M4/M5 as predicted in various ‘cool-water’ scenarios. In short, these results do not support a shift to ‘cool-water’ conditions as an explanation for changes in early Katian carbonates across the M4/M5.

Maastrichtian strata of the Zumaya-Algorta Formation of southwestern France and northeastern Spain record a major pulse of extinction among inoceramid bivalves well before the Cretaceous–Tertiary (K–T) boundary. Inoceramids are the most abundant macrofossils preserved in the study sections; at least six species of Inoceramus [I. (Endocostea) aff. I. (En.) balticus Giers, I. (En.) pteroides Giers, I. (Platyceramus) aff. I. (Pl.) cycloides Wegner, I. (Trochoceramus) nahorianensis Kociubynskij, I. (Tr.) morgani Sornay, and I.(?) goldfussianus d'Orbigny] are common to abundant in lower Maastrichtian strata. However, all six species disappear over a few tens of meters of section near the base of the upper Maastrichtian, as defined by the first appearance of the planktonic foraminifer Abathomphalus mayaroensis. Tenuipteria argentea (Conrad), which has not been recovered from the lower Maastrichtian portions of the sections, occurs at low abundances through the upper Maastrichtian, disappearing within 10 cm of the K–T boundary.

The mid-Maastrichtian extinction interval among inoceramids occurs within the upper Globotruncana gansseri to lower Abathomphalus mayaroensis planktonic foraminiferal zone, in nannofossil zone 24 to 25A, in the Anapachydiscus fresvillensis ammonite zone, in magnetochron 31N, and near the base of a change in slope of the seawater strontium curve, all as recognized by previous studies in one or more of the study sections. Whereas the new data presented here are not global in extent, the observed distribution of inoceramids may be the local manifestation of global oceanic changes during the mid-Maastrichtian.

New mid-Cretaceous stable isotope (δ18O and δ13C) records of multiple planktonic foraminiferal species and coexisting coccoliths from Blake Nose (western North Atlantic) document a major depth-ecology reorganization of planktonic foraminifera. Across the Albian/Cenomanian boundary, deep-dwelling Praeglobotruncana stephani and Rotalipora globotruncanoides adapted to living at a shallower depth, while, at the same time, the population of surface-dwelling Paracostellagerina libyca declined. Subsequently, the opportunistic species Hedbergella delrioensis shifted to a deep environment, and the deep-dwelling forms Rotalipora montsalvensis and Rotalipora reicheli first appeared. The primary paleoenvironmental cause of the observed changes in planktonic adaptive strategies is uncertain, yet their coincidence with an earliest Cenomanian cooling trend reported elsewhere implicates the importance of reduced upper-ocean stratification. Although there has been an implicit assumption that the species-specific depth habitats of fossil planktonic foraminifera were invariant through time, planktonic paleoecology is a potential variable. Accordingly, the possibility of evolutionary changes in planktonic foraminiferal depth ecology should be a primary consideration (along with other environmental parameters) in paleoceanographic interpretations of foraminiferal stable isotope data.

After having been very abundant in the Early Maastrichtian Globotruncana gansseri zone, Inoceramus remains disappear from five stratigraphic sections in the Basque region of France and Spain in the lower Abathomphalus mayaroensis zone, ~2.5 m.y. before the Cretaceous–Tertiary boundary. Several lines of evidence demonstrate that these shell fragments are preserved in place and accurately record the pattern of the decline and disappearance of the group. The dominant taphonomic process seems to have been passive disaggregation of the shell as shell proteins decayed. The resulting shell fragments were dispersed only locally by burrowing organisms. Shell fragments decline in abundance over tens of meters of section and there are subtle differences between sections which suggests Inoceramus was eliminated by gradual changes in ecological conditions that affected the basin roughly simultaneously but with some geographic variability.

Oxygen isotopic analysis of the phosphate in bioapatite has become a standard paleoclimatological tool with results documented in a rapidly expanding literature. Phosphate-based measurements are particularly important for samples where carbonates preservation is suspect (as is the case for many Paleozoic sites). Important analytical and observational advances that have fueled the expansion of phosphate-based studies include: 1) Oxygen isotopic ratios of biogenic apatite can be measured on small enough samples (≥ ~300 μg), quickly enough, cheaply enough, and accurately enough to permit meaningful high resolution paleoclimatic studies of trends through time, along spatial transects, and/or among taxa, 2) biogenic apatite is precipitated in approximate equilibrium with ambient waters and thus records the interplay of temperature and the isotopic composition of the water in which a sample grew, 3) tooth enamel and conodont crown material are quite resistant to diagenetic alteration and are preferred targets for both paleotemperature and paleoecological studies, 4) Paleozoic conodont δ18O records seem to provide robust paleotemperature information on time scales ranging from thousands of years to 100's of millions of years, and generation of increasingly refined paleotemperature records from this diagenetically resistant phase is likely to continue to be a useful field of study, 5) paleoenvironmental variations in δ18O values of seawater have been documented (e.g., differences between glacial and interglacial oceans), but whether and by how much the δ18O value of the hydrosphere may have increased since the Cambrian remains unresolved, and 6) differences in δ18O values among conodont taxa are increasingly well documented and, coupled with the potential to study growth series using ion microprobe techniques, are providing novel perspectives on and important tests of conodont paleoecology.