Evolution of planktic organisms from benthic ancestors is commonly thought to represent unidirectional expansion into new ecological domains, possibly only once per clade. For foraminifera, this evolutionary expansion occurred in the Early-Middle Jurassic, and all living and extinct planktic foraminifera have been placed within 1 clade, the Suborder Globigerinina. The subsequent radiation of pl...

Fossils of marine microorganisms such as planktic foraminifera are among the cornerstones of palaeoclimatological studies. It is often assumed that the proxies derived from their shells represent ocean conditions above the location where they were deposited. Planktic foraminifera, however, are carried by ocean currents and, depending on the life traits of the species, potentially incorporate di...

Larger symbiont-bearing foraminifera are prominent and important producers of calcium carbonate in modern tropical environments. With an estimated production of at least 130 million tons of CaCO(3) per year, they contribute almost 5% of the annual present-day carbonate production in the world's reef and shelf areas (0-200 m) and approximately 2.5% of the CaCO(3) of all oceans. Together with non...

The geochemical composition of foraminiferal tests is a valuable archive for the reconstruction of paleo-climatic, -oceanographic and -ecological changes. However, dissolution of biogenic calcite and precipitation of inorganic calcite (overgrowth and recrystallization) at the seafloor and in the sediment column can potentially alter the original geochemical composition of the foraminiferal test...

A series of recent papers has called for multiple radiocarbon dates on planktic foraminifera to assess stratigraphic continuity in deep-sea sediment cores. This recommendation comes from observations of anomalous 14C dates in planktic foraminifera from the same stratigraphic level. Potential reasons include bioturbation, downslope transport, secondary calcification, carbonate dissolution, and d...

The relationship between seawater temperature and the average Mg/Ca ratios in planktic foraminifera is well established, providing an essential tool for reconstructing past ocean temperatures. However, many species display alternating high and low Mg-bands within their shell walls that cannot be explained by temperature alone. Recent experiments demonstrate that intrashell Mg variability in Orb...

The geochemical composition of foraminiferal tests is a valuable archive for the reconstruction of paleo-climatic, -oceanographic and -ecological changes. However, dissolution of biogenic calcite and precipitation of inorganic calcite (overgrowth and recrystallization) at the seafloor and in the sediment column can potentially alter the original geochemical composition of the foraminiferal test...

Assessing the extent to which population subdivision during cladogenesis is necessary for long-term phenotypic evolution is of fundamental importance in a broad range of biological disciplines. Differentiating cladogenesis from anagenesis, defined as evolution within a species, has generally been hampered by dating precision, insufficient fossil data, and difficulties in establishing a direct l...

Planktic foraminifera have traditionally been classified within a single order: Globigerinida. However, recent phylogenetic studies, both molecular and stratophenetic, are evidencing the polyphyletic origin of planktic from several benthic ancestors. At least four independent events benthic-planktic transition identified. One them occurred after Cretaceous–Paleogene boundary mass extincti...

[1] In recent years it has become apparent that the ‘‘cool tropic paradox’’ of Paleogene and Cretaceous ‘‘greenhouse’’ climates arises because of the diagenetic alteration of tropical planktic foraminiferal calcite near the seafloor, yielding artificially high dO values. Because the Mg/Ca compositions of foraminiferal and inorganic calcite are thought to be quite different, Mg/Ca measurements s...