281 research outputs found
Interannual variability of planktic foraminiferal populations and test flux in the eastern North Atlantic Ocean
Planktic foraminiferal assemblages vary in response to seasonal fluctuations of hydrographic properties, between water masses, and after periodical changes and episodic events (e.g. reproduction, storms). Distinct annual variability of the planktic foraminiferal flux is also known from sediment trap data. In this paper we discuss the short-term impacts on interannual flux rates based on data from opening–closing net hauls obtained between the ocean surface and 500 m water depth. Data were recorded during April, May, June, and August at around 47°N, 20°W (BIOTRANS) in 1988, 1989, 1990, 1992, 1993, and during May 1989 and 1992 at 57°N, 20–22°W. Species assemblages closely resemble each other when comparing the mixed layer fauna with the fauna of the upper 100 m and the upper 500 m of the water column. In addition, species assemblages >100 ?m are almost indistinguishable from assemblages that are >125 ?m in test size. The standing stock of planktic foraminifers at BIOTRANS can vary by more than one order of magnitude over different years; however, species assemblages may be similar when comparing corresponding seasons. Early summer assemblages (June) are distinctly different from late summer assemblages (August). Significant variations in the species composition during spring (April/May) are independent of the mixed layer depth. Spring assemblages are characterized by high numbers of Globigerinita glutinata. In particular, day-to-day variations of the number of specimens and in species composition may have the same order of magnitude as interannual variations. This appears to be independent of the reproduction cycle. Species assemblages at 47°N and 57°N are similar during spring, although surface water temperatures and salinities differ by up to 10°C and 0.7 (PSU). We suggest that the main factors controlling the planktic foraminiferal fauna are the trophic properties in the upper ocean productive layer.Planktic foraminiferal carbonate flux as calculated from assemblages reveals large seasonal variations, a quasi-annual periodicity in flux levels, and substantial differences in timing and magnitude of peak fluxes. At the BIOTRANS station, the average annual planktic foraminiferal CaCO3 fluxes at 100 and 500 m depth are estimated to be 22.4 and 10.0 gm?2 yr?1, respectively
Modern planktic foraminifera
Planktic foraminifers are marine protozoans with calcareous Shells and chambered tests. They first appeared in the mid-Jurassic and spread since the mid-Cretaceous over all the world’s oceans. Modern planktic foraminifers evolved since the early Tertiary, when the first spinose species occurred. Most species live in the surface to sub-thermocline layer of the open ocean, and in marginal seas like the Mediterranean, Caribbean, South China Sea, and Red Sea. Planktic foraminifers are absent in shallow marginal seas, for example, the North Sea. Planktic foraminifers respond to food, temperature and chemistry of the ambient seawater. Species abundance varies according to seasons, water masses, and water depths. Symbiont-bearing species depend on light and are restricted to the euphotic zone. Planktic foraminifers constitute a minor portion of total Zooplankton, but are major producers of marine calcareous particles (shells) deposited on the ocean floor where they form the so-called foraminiferal ooze.Planktic foraminifers contribute substantially to the fossil record of marine Sediments and are of high ecologic, paleoceanographic, and stratigraphic significance since the mid-Cretaceous. Radiocarbon (14C) gives an absolute age of shell formation within late Pleistocene and Holocene Sediments. Factors that determine the modern faunal composition are applied to Interpretation of the fossil assemblages, for example, by multiple regression techniques (transfer functions) to yield an estimate on ancient environmental parameters. The chemical composition of the calcareous shell (stable isotopes and trace elements) holds clues to the chemical and physical State of the ambient seawater and is useful in the reconstruction of temperature, chemical State, and biological productivity of the ancient marine environment
Early Maastrichtian benthic foraminiferal assemblages from the western North Atlantic (Blake Nose) and their relation to paleoenvironmental changes
Benthic foraminiferal faunas from the Lower Maastrichtian (Globotruncana falsostuarti–Gansserina gansseri Planktic Foraminiferal Zone) of DSDP Site 390 (Blake Nose, western North Atlantic) were investigated in order to characterize changes in organic matter flux and bottom-water oxygenation and their relation to paleoceanographic changes. Benthic foraminiferal faunas in the lower part of the studied succession show high abundances of Praebulimina reussi and Nuttallides truempyi and are proposed to reflect fluctuations in organic matter flux to the seafloor (meso- to eutrophic) under oxygenated bottom-water conditions. The middle interval is characterized by very low numbers of benthic foraminiferal specimens but a dominance of thick-walled species (e.g., lenticulinids, laevidentalinids), may reflect carbonate dissolution. In contrast to the lower part, benthic foraminifera from the upper part of the succession show well-oxygenated bottom waters. The most dominant species during this interval are Gavelinella beccariiformis, Reussella szajnochae, and N. truempyi. Parallel to this change in the benthic foraminiferal assemblages the number of inoceramid shells decreases, reflecting a significant increase in bottom-water oxygenation. Based on these data we speculate, that the observed changes in benthic foraminiferal assemblages towards a well-oxygenated environment within the Early Maastrichtian of DSDP Site 390 could reflect the onset of a shift from low-latitude to high-latitude deep-water sources. This speculation will predate the major reorganization of the oceanic circulation resulting in a circulation mode similar to today at the Early/Late Maastrichtian boundary by 1 Ma. <br/
Agglutinated Foraminifera: An Introduction
Unicellular protozoans are among the oldest fossils which we can recognize from the Precambrian. Presumably, foraminiferal ancestors were among the earliest of them, but had not yet benefitted from being sheltered by a biomineralized test. During the earliest Cambrian the first agglutinating foraminifera made their first appearance in the geologic record. These “primitive” forms built their test of foreign particles held together by an organic cement. This organic cement may have been secreted by the foraminifer in cytoplasmic vacuoles as is the case with Recent agglutinating foraminifera. Yet, the capability to biomineralize calcite did not evolve until after another 60 million years when the fusulinids developed their microgranular wall. Calcitic cemented agglutinates occur even later, at the base of the Carboniferous. Thus, in the fossil record the agglutinated foraminifera occur as a twofold group with a rather distinct evolution
Three hundred eighty thousand year long stable isotope and faunal records from the Red Sea : influence of global sea level change on hydrography
Stable isotope and faunal records from the central Red Sea show high-amplitude oscillations for the past 380,000 years. Positive δ18O anomalies indicate periods of significant salt buildup during periods of lowered sea level when water mass exchange with the Arabian Sea was reduced due to a reduced geometry of the Bab el Mandeb Strait. Salinities as high as 53‰ and 55‰ are inferred from pteropod and benthic foraminifera δ18O, respectively, for the last glacial maximum. During this period all planktonic foraminifera vanished from this part of the Red Sea. Environmental conditions improved rapidly after 13 ka as salinities decreased due to rising sea level. The foraminiferal fauna started to reappear and was fully reestablished between 9 ka and 8 ka. Spectral analysis of the planktonic δ18O record documents highest variance in the orbital eccentricity, obliquity, and precession bands, indicating a dominant influence of climatically - driven sea level change on environmental conditions in the Red Sea. Variance in the precession band is enhanced compared to the global mean marine climate record (SPECMAP), suggesting an additional influence of the Indian monsoon system on Red Sea climates
New constraints on the timing and amplitude of sea level fluctuations during early to middle Marine Isotope Stage 3
To settle debate on the timing of sea level fluctuations during Marine Isotope Stage (MIS) 3, we present records of ?18Oruber (sea level proxy) and magnetic susceptibility from the same samples within the single sediment archive (i.e., ‘co-registered’) of central Red Sea core GeoTü-KL11. Core-scanning X-ray fluorescence and environmental magnetic data establish the suitability of magnetic susceptibility as a proxy for eolian dust content in Red Sea sediments. The eolian dust data record similar variability as Greenland ?18Oice during early to middle MIS 3, in agreement with previous observations that regional Arabian Sea climate fluctuated with a timing similar to that of Greenland climate variations. In contrast, the sea level record fluctuates with a timing similar to that of Antarctic-style climate variations. The co-registered nature of the two records in core KL11 unambiguously reveals a distinct offset in the phase relationship between sea level and eolian dust fluctuations. The results confirm that sea level rises, indicated by shifts in Red Sea ?18Oruber to lighter values, occurred during cold episodes in Greenland during early to middle MIS 3. This indicates that the amplitudes of the reconstructed MIS 3 sea level fluctuations would not be reduced by inclusion of regional climate fluctuations in the Red Sea sea level method. Our analysis comprehensively supports our earlier conclusions of large-amplitude sea-level variations during MIS 3 with a timing that is strongly similar to Antarctic-style climate variations
Climatic changes in the Late Campanian - Early Maastrichtian: micropaleontological and stable isotopic evidence from an epicontinental sea
Planktic foraminiferal production stimulated by chlorophyll redistribution and entrainment of nutrients
During September and October 1996 planktic foraminifers and pteropods were sampled from the upper 2500 m of the water column in the BIOTRANS area (47°N, 20°W), eastern North Atlantic, as part of the JGOFS program. Hydrography, chlorophyll fluorescence, and nutrient content were recorded at high spatial and temporal resolution providing detailed information about the transition time between summer and fall. At the beginning of the cruise a shallow pycnocline was present and oligotrophic conditions prevailed. Over the course of the cruise, the mixed layer depth increased and surface water temperature decreased by 1.5°C. Both chlorophyll-a dispersed in the upper 50 m by vertical mixing and chlorophyll-a concentrations at the sea surface increased. The nitracline shoaled and nutrient enriched waters were entrained into the mixed layer. Planktic foraminifers and pteropods closely reflected the changes in the hydrography by increased growth rates and changes in species composition. Three main groups of planktic foraminiferal species were recognized: (1) a temperate and low-productivity group dominated by Neogloboquadrina incompta characterized the shallow mixed layer depths. (2) A temperate and high-productivity group dominated by Globigerina bulloides characterized the period with wind-induced dispersal of chlorophyll-a and entrainment of nutrient-enriched waters. (3) A warm water group containing Globigerinoides sacculifer, Orbulina universa, Globigerinoides ruber (white), and Globigerinella siphonifera was most common during the first days of sampling. Synchronous with the hydrographic change from summer to fall, planktic foraminiferal and pteropod growth was stimulated by redistribution of chlorophyll-a and entrainment of nutrient-enriched waters into the mixed layer. In addition, the seasonal change in the eastern North Atlantic resulted in a transition of the epipelagic faunal composition and an increased calcareous particle flux, which could be used to trace seasonality in fossil assemblages and allow for better paleoceanographic interpretation of the boreal Atlantic
Tracking the Recent and late Pleistocene Azores front by the distribution of planktic foraminifers
South of the Azores Islands, the population dynamics and sedimentation of planktic foraminifers are significantly influenced by the hydrography of the Azores Front Current System (AFCS). Planktic foraminifers collected from the water column during seasonal cruises across the Azores Front, record the temporal and spatial scale of hydrographic and faunal dynamics within this area. Surface sediment analysis reveals the presence of a large number of pteropod shells indicating preservation of aragonite and, therefore, little alteration of the calcitic foraminiferal tests. Consequently, most of the seasonal and spatial variability of the Azores Front is expected to be recorded by the planktic foraminiferal assemblages present within the surface sediment. In particular, Globorotalia scitula, a subsurface-dwelling species, decreases significantly in abundance to the south of the Azores Front, and shows fine-scale changes at the glacial/interglacial time scale. Enhanced faunal proportions of G. scitula in a sediment core that is located to the south of the modern Azores Current indicate a southward shift of the Azores Front Current System during the glacials and the presence of a transitional water mass at the Azores region. <br/
Taxonomy, biostratigraphy, and phylogeny of Oligocene and lower Miocene Globoturborotalita
The taxonomy, phylogeny and biostratigraphy of
Oligocene and lower Miocene Globoturborotalita is
reviewed. Globoturborotalita is a long-ranging genus appearing in the basal Eocene and still present
in modern oceans with one living representative G.
rubescens. Species attributed to this genus are generally common and cosmopolitan. The following
species are recognized as valid: Globoturborotalita
barbula Pearson and Wade, Globoturborotalita bassriverensis Olsson and Hemleben, Globoturborotalita brazieri (Jenkins), Globoturborotalita cancellata
(Pessagno), Globoturborotalita connecta (Jenkins), Globoturborotalita eolabiacrassata Spezzaferri and
Coxall n. sp., Globoturborotalita euapertura (Jenkins), Globoturborotalita gnaucki (Blow and Banner), Globoturborotalita labiacrassata (Jenkins),
Globoturborotalita martini (Blow and Banner),
Globoturborotalita occlusa (Blow and Banner), Globoturborotalita ouachitaensis (Howe and Wallace),
Globoturborotalita paracancellata Olsson and Hemleben n. sp., Globoturborotalita pseudopraebulloides
Olsson and Hemleben n. sp., and Globoturborotalita
woodi (Jenkins)
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