Description: Six spinose species of planktonic foraminifera (Hastigerina pelagica (d'Orbigny), Globigerinella aequilateralis (Brady), Globigerinoides ruber (d'Orbigny), Globigerinoides sacculifer (Brady), Globigerinoides conglobatus (Brady) and Orbulina universa d'Orbigny) are routinely collected by scuba diving in the Sargasso Sea off Bermuda and are maintained in the laboratory. These and non-spinose species can also be collected with plankton nets for laboratory culture. H. pelagica recovers extremely well from the net-towing operation. The mean survival times of H. pelagica, G. aequilateralis, G. ruber, G. sacculifer, G. conglobatus and O. universa in laboratory cultures are 21.1, 10.6, 6.2, 6.7, 11.8 and 8.8 days, respectively. These figures reflect in part the onset of gametogenesis, which terminates the life of the mother cell. During gametogenesis, which occurs over a period of about thirteen hours, the mother shell sinks and sheds its spines, and hundreds of thousands of gametes are released. Gametogenesis has been observed in nine species. All six spinose species possess one or more types of associated algae, which vary widely in size and number. The external ones are large dinoflagellates, such as Pyrocystis fusiformis, P. noctiluca and Dissodinium spp., which occur with H. pelagica. The smaller ones (zooxanthellae) in G. sacculifer, G. ruber and O. universa exhibit a circadian periodicity of ingress into the shell in the evening and egress to the rhizopodial network and the distal parts of the spines during the day. Some planktonic foraminiferal species are herbivorous, others are carnivorous, and still others are omnivorous. Copepods appear to be the main diet of G. aequilateralis and H. pelagica, both of which are fed Artemia nauplii in the laboratory. Shell and spine growth have been observed, and the formation of a new chamber in G. ruber takes place in about 90 minutes.

Description: We report direct δ44Ca-temperature calibration on cultured and fossil calcite foraminifera, showing that Ca isotopes are potentially a new proxy for past sea surface temperatures (SST). Samples have been analyzed using a 43Ca-48Ca double spike and thermal ionization mass spectrometry (TIMS). In order to avoid species-dependent isotope fractionation we focused our investigations on a single foraminifera species (Globigerinoides sacculifer), which is known to inhabit shallow euphotic waters in tropical and subtropical oceans. Ca isotope measurements were performed on cultured G. sacculifer that grew in seawater kept at temperatures of 19.5°, 26.5°, and 29.5°C. A δ44Ca change of 0.24 ± 0.02 per 1°C is defined by the weighted linear regression through reproduced δ44Ca data of the three temperatures (95% confidence level). Application of this new method to fossil G. sacculifer of an Equatorial East Atlantic sediment core (GeoB1112; 5°46.7′S, 10°45.0′W, 3125 m) indicates that the δ44Ca difference between marine isotope stage 1 (MIS-1) and MIS-2 is 0.71 ± 0.24. According to the current δ44Ca-temperature calibration this value corresponds to a temperature difference between MIS-1 and MIS-2 of ∼3.0 ± 1.0°C.

Description: We critically evaluate the applicability of Ca-isotope ratios in planktonic foraminifers as proxy for past sea surface temperatures (SST) and isotope composition of paleo-seawater (δ44Casw) reconstructions. Previous studies have shown discrepancies regarding the temperature sensitivity of Ca isotope fractionation in foraminifers of more than one order of magnitude. We present new data from the planktonic foraminifer species Orbulina universa, Globigerinoides sacculifer and Neogloboquadrina pachyderma (sinistral) from culture experiments, multinet deployments and coretop samples. Specimens of G. sacculifer cultured at low salinities (33–34.5) show predominantly no major temperature dependent Ca isotope fractionation, in contrast to previous individuals cultured at higher salinities of 34.5–36. The new data of O. universa are consistent with previously published results, revealing a small but significant temperature sensitivity. Calcium isotope fractionation in tests of N. pachyderma shows a significant variation with temperature, which is not uniform over the total investigated temperature range (−1.6 °C to +10 °C), possibly reflecting the influence of additional controlling factors besides temperature. Controlled dissolution experiments in the laboratory indicate that the Ca-isotope composition of G. sacculifer and N. pachyderma is relatively insensitive to partial dissolution of their tests. Calcium isotope ratios in the planktonic foraminifers G. sacculifer and N. pachyderma (s) reveal a complex Ca isotope fractionation behaviour, which is not yet fully understood. Additional validation studies are crucial to enhance the basic understanding of the calcium isotope systematics in planktic foraminifer shells, and the potential for applying Ca-isotope ratios as proxies for seawater temperature and the oceanic Ca budget.

Description: In a midoceanic region of the northeast Atlantic, patches of freshly deposited phytodetritus were discovered on the sea floor at a 4500 m depth in July/August 1986. The color of phytodetritus was variable and was obviously related to the degree of degradation. Microscopic analyses showed the presence of planktonic organisms from the euphotic zone, e.g., cyanobacteria, small chlorophytes, diatoms, coccolithophorids, silicoflagellates, dinoflagellates, tintinnids, radiolarians, and foraminifers. Additionally, crustacean exuviae and a great number of small fecal pellets, “minipellets,” were found. Although bacteria were abundant in phytodetritus, their number was not as high as in the sediment. Phytodetrital aggregates also contained a considerable number of benthic organisms such as nematodes and special assemblages of benthic foraminifers. Pigment analyses and the high content of particulate organic carbon indicated that the phytodetritus was relatively undegraded. Concentrations of proteins, carbohydrates, chloroplastic pigments, total adenylates, and bacteria were found to be significantly higher in sediment surface samples when phytodetritus was present than in equivalent samples collected at the same stations in early spring prior to phytodetritus deposition. Only the electron transport system activity showed no significant difference between the two sets of samples, which may be caused by physiological stress during sampling (decompression, warming). The chemical data of phytodetritus samples displayed a great variability indicative of the heterogeneous nature of the detrital material. The gut contents of various megafauna (holothurians, asteroids, sipunculids, and actiniarians) included phytodetritus showing that the detrital material is utilized as a food source by a wide range of benthic organisms. Our data suggest that the detrital material is partly rapidly consumed and remineralized at the sediment surface and partly incorporated into the sediment. Incubations of phytodetritus under simulated in situ conditions and determination of the biological oxygen demand under surface water conditions showed that part of its organic matter can be biologically utilized. Based on the measured standing stock of phytodetritus, it is estimated that 0.3–3% of spring primary production sedimented to the deep-sea floor. Modes of aggregate formation in the surface waters, their sedimentation, and distribution on the seabed are discussed.