Dissertations / Theses on the topic 'Foraminifera'
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Lundquist, Jason James. "Foraminiferal biostratigraphic and paleoceanographic analysis of the Eagle Ford, Austin, and Lower Taylor groups (Middle Cenomanian through Lower Campanian) of central Texas /." Digital version accessible at:, 2000. http://wwwlib.umi.com/cr/utexas/main.
Full textBuchan, Olivia Claire Lewis Ronald D. "Relationships between large benthic foraminifera and their seagrass habitats, San Salvador, Bahamas." Auburn, Ala., 2006. http://repo.lib.auburn.edu/2006%20Spring/master's/BUCHAN_OLIVIA_31.pdf.
Full textCaromel, Aude Genevieve Marcelle. "Form and function in planktic foraminifera." Thesis, University of Bristol, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.628998.
Full textPearson, Paul Nicholas. "Evolution and phylogeny of Palaeogene planktonic foraminifera." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386154.
Full textSeears, Heidi. "Biogeography and phylogenetics of the planktonic foraminifera." Thesis, University of Nottingham, 2011. http://eprints.nottingham.ac.uk/11879/.
Full textWard, Juliette Natalie. "Foraminifera as proxiles for monitoring organic pollution." Thesis, University of Southampton, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398830.
Full textAl-Sayigh, Abdul Razak Siddiq. "Lower Tertiary Foraminifera from south east Oman." Thesis, Aberystwyth University, 1999. http://hdl.handle.net/2160/1a8d5b93-df4b-412e-aecb-38c02de78e03.
Full textCoxall, Helen Katherine. "Hantkeninid planktonic foraminifera and Eocene palaeoceanographic change." Thesis, University of Bristol, 2000. http://hdl.handle.net/1983/8efa1d22-0ff8-45a3-9a5c-bd5ea90e266f.
Full textLicari, Laetitia. "Ecological preferences of Benthic Foraminifera in the Eastern South Atlantic : distribution patterns, stable carbon isotopic composition, and paleoceanographic implications = Ökologische Ansprüche benthischer Foraminiferen im östlichen Südatlantik /." Bremerhaven : Alfred-Wegener-Inst. für Polar- und Meeresforschung, 2006. http://www.gbv.de/dms/bs/toc/514912308.pdf.
Full textHudson, Wendy. "The evolution and palaeobiogeography of Mesozoic planktonic foraminifera." Thesis, University of Plymouth, 2007. http://hdl.handle.net/10026.1/719.
Full textChapman, Mark Robert. "Late Pliocene planktonic foraminifera : palaeoceanography and faunal evolution." Thesis, University of East Anglia, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.332388.
Full textKhanna, Nikki. "The biological response of foraminifera to ocean acidification." Thesis, University of St Andrews, 2014. http://hdl.handle.net/10023/8089.
Full textDos, Santos Francisco Kelmo Oliveira. "Ecological consequences of the 1997-98 El Niño Southern Oscillation on the major coral reef communities from northern Bahia, Brazil." Thesis, University of Plymouth, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.246378.
Full textSpeed, Craig Duncan. "High-resolution palaeoceanography of extreme early Pliocene carbonate-opal cycles in the eastern equatorial Pacific." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274423.
Full textBordelon, Laura Anne. "AUSTRAL AUTUMN AND WINTER SEASONAL AFFECTS ON BENTHIC FORAMINIFERAL COMMUNITIES: BRANSFIELD AND NORTHERN GERLACHE STRAITS." OpenSIUC, 2009. https://opensiuc.lib.siu.edu/theses/150.
Full textHurley, John Vincent. "Late-middle Eocene glacioeustacy : evidence from stable isotopes and foraminifera of the the [sic] Planktonic foraminiferan zone P14 (Truncorotaloides rohri zone), Mossy Grove Core, Hinds County, Mississippi." Virtual Press, 1999. http://liblink.bsu.edu/uhtbin/catkey/1117851.
Full textDepartment of Geology
Vicedo, Vicedo Vicent. "Morfoestructura de los géneros cretácicos de los Rhapydioninidae (Foraminifera)." Doctoral thesis, Universitat Autònoma de Barcelona, 2008. http://hdl.handle.net/10803/3447.
Full textPara llevar a cabo la revisión de los taxones, se han muestreado las localidades tipo o, cuando ha sido imposible, las localidades equivalentes siempre lo más cercanamente posible a las localidades tipo. En México, para el muestreo se han seguido las indicaciones y descripciones estratigráficas de Pêcheux (1984) y Michaud (1987). En España, se han considerado los trabajos de Martín-Chivelet (1993) para la Cordillera Bética y Calonge (1989) para la Cordillera Ibérica. En Grecia se han seguido los trabajos de Fleury (1974), mientras que el material de Italia fue recolectado por Mariano Parente en los Apeninos. Todos los rapidionínidos proceden de sedimentos extraordinariamente poco profundos. Por consiguiente, su restringido nicho ecológico dificulta una correlación precisa con la escala cronoestratigráfica en general y con la escala biostratigráfica basada en biozonaciones de orbitoídidos en particular. En consecuencia, algunas de las conclusiones taxonómicas dadas a nivel específico se deben considerar provisionales o tentativas. Los resultados de este trabajo confirman en gran medida las observaciones realizadas por Fleury y Fourcade en su trabajo de 1990, el único trabajo publicado en el que se da una visión general del grupo de los rapidionínidos desde que Henson publicara, en 1948, su monografía.
The rhapydioninids represent an important, diverse and abundant element in the shallow-water communities of porcelaneous foraminifera of the Middle and Late Cretaceous. Their general morphology is very similar and called for a careful morphological analysis in order to distinguish the genera and the species within the different groups involved. The revision of the relevant taxa given here permits to eliminate contradictions and inconsistencies in the current literature, to enhance their potential as biostratigraphic index fossils and to understand the significance of their paleogeographic distribution. In particular, the use of the generic name Pseudedomia Henson, 1948, (type species: P. multistriata, Maastrichtian) for species belonging to the previous Global Community Maturation cycle (Hottinger, 2001), such as "P." drorimensis Reiss et al., 1964, (Cenomanian) or the supposed synonymy of the Caribbean Raadshoovenia guatemalensis van den Bold, 1946, (said to be of Paleocene age) with the Tethyan Cuvillierinella salentina Papetti and Tedeschi, 1965, (Late Cretaceous) have produced considerable difficulties to understand the evolution of the rhapydioninid family in time and space.
In order to revise the various taxa involved, their type localities or as close equivalents as possible where sampled. In Mexico the stratigraphical descriptions and indications of Pêcheux (1984) and Michaud (1987) were followed. In Spain, we could relay on the work of Martin-Chivelet (1993) for the Betic Cordillera and of Calonge (1989) for the Iberian range. In Greece we founded our sampling on the papers of Fleury (1974), whereas in Italy Mario Parente collected suitable material for our research from the Apennines. All rhapydioninids are found in sediments with an extremely very shallow facies. Thus, their restricted ecological range often hampers a precise correlation with the chronostratigraphic time scale in general and with the ecologically closest biostratigraphic zonation based on orbitoids in particular. Therefore, some of the taxonomic conclusions on the species level must be considered as provisional or tentative. The results of the revisions given here confirm to a large extent the views expressed by Fleury and Fourcade in their paper of 1990, the only comprehensive overview on the group to be found in literature since Henson's monograph in 1948.
Bryan, Sean Patrick. "Calibration of trace element paleoceanographic proxies in benthic foraminifera." Connect to online resource, 2007. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:1446083.
Full textAze, Tracy. "Cope's rule and macroevolution of Cenozoic macroperforate planktonic foraminifera." Thesis, Cardiff University, 2011. http://orca.cf.ac.uk/22350/.
Full textKelham, Angela. "Investigation into the post-mortem transport of benthic foraminifera." Thesis, University of Hull, 2011. http://hydra.hull.ac.uk/resources/hull:5473.
Full textEvans, John Rhys. "Late Neogene agglutinated foraminifera from the central Arctic Ocean." Thesis, University College London (University of London), 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.267751.
Full textKaminski, Michael Anthony. "Cenozoic deep-water agglutinated foraminifera in the North Atlantic." Thesis, Massachusetts Institute of Technology, 1987. http://hdl.handle.net/1721.1/55312.
Full textVita.
Includes bibliographical references (p. 243-259).
by Michael Anthony Kaminski.
Ph.D.
Rode, Sandra Lee 1955. "FORAMINIFERA AS A TEST OF HERITABILITY OF SPECIATION POTENTIAL." Thesis, The University of Arizona, 1987. http://hdl.handle.net/10150/276479.
Full textPazio, Magdalena. "The late Ediacaran Agglutinated Foraminifera from Finnmark, Northern Norway." Thesis, Uppsala universitet, Institutionen för geovetenskaper, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-183994.
Full textStewart, Duncan Ross McIver. "Evolution of Neogene globorotaliid foraminifera and Miocene climate change." Thesis, University of Bristol, 2003. http://hdl.handle.net/1983/2bd17901-2015-41b6-b43a-acb79c9cdf44.
Full textPettit, Laura Rachel. "The effects of ocean acidification on modern benthic foraminifera." Thesis, University of Plymouth, 2015. http://hdl.handle.net/10026.1/3465.
Full textBowen, Powell Jacqueline. "Larger Foraminiferal Biostratigraphy, Systematics And Paleoenvironments of The Avon Park Formation and Ocala Limestone, Highlands County, Florida." FIU Digital Commons, 2010. http://digitalcommons.fiu.edu/etd/288.
Full textJulian, Meaghan Elizabeth. "Benthic foraminiferal faunal changes during the Eocene/Oligocene climate transition at Ocean Drilling Program (ODP) sites 1209A and 1211A from the Shatsky Rise, central Pacific Ocean." Thesis, [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-1519.
Full textEdwards, Robin James. "Late Holocene relative sea level change and climate in southern Britain." Thesis, Durham University, 1998. http://etheses.dur.ac.uk/1056/.
Full textGroves, Daniel James. "HOLOCENE FORAMINIFERAL ASSEMBLAGE AND STABLE ISOTOPE ANALYSIS FOR THE GERLACHE STRAIT, ANTARCTIC PENINSULA." OpenSIUC, 2015. https://opensiuc.lib.siu.edu/theses/1642.
Full textArriaga, Cavalieri Maria Eugenia. "Patrones de supervivencia y recuperación de los macroforaminíferos después de la extinción en masa del límite Cenomaniense-Turoniense." Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/394041.
Full textLarger foraminifera are a k-strategists group extremely abundant in shallow water plat¬form environments, both in the recent and the fossil record. They represent one of the most sensitive marine organisms to environmental perturbations. During the Cenomanian-Turonian Boundary (CTB) interval, coinciding with a widespread episode of organic-rich sediments deposition (Oceanic Anoxic Event 2 or Bonarelli event), the larger foraminifera inhabiting the shallow environment were dramatically affected by a major paleoenvironmental conditions change. Such event finished with the middle Cretaceous Glo¬bal Community Maturation Cycle (GCMC). In this work we discuss the post-extinction recovery pattern. This works has been carried out in two neighboring paleoprovinces: Central Tethys, which outcrop at the southern Appenines, and the Pyrenean, outcrop located at the southern Pyrenees (Central Sud-pyrenean Unit). In the Pyrenees, like in most of the platforms, the water layer suffered an eutrophication process that leads demise the carbonate producer organisms, causing a stop on carbonate sedimentation. Such lack on sedimentation generates a sedimen¬tary hiatus perceptible in the stratigraphic record before the drowning episode. While the platform from southern Apennines was able to keep up on shallow carbonate sedimentation, and despite the colonization of cyanobacteria organisms, some small foraminifera were capa¬ble to survive. Here is suggest that even though the paleogeographic and depositional differences bet¬ween the studied areas, both present similar recovery patterns in the fallowing way: 1) The genetic information necessary for sustaining a k-strategy was lost with the extinction, but the “legacy” of larger foraminifera survived in the small r-strategist forms of Nezzazatinella, Cu¬neolina, Dictyopsella and Rotorbinella survivor genus. 2) chronostratigraphic calibration of Apenninic sections made by Strontium and Carbon Isotopic Stratigraphic data, indicates that the firth “newcomers ” appears during the upper part of lower Turonian with Moncharmontia apenninica and Pseudocyclammina spharoidea new species; but is not until middle-upper Tu¬ronian that more complex forms appears with Scandonea samnítica and Reticulinella kaeveri species. 3) In the Pyrenees, the shallow foraminiferal fauna reenter during the mid-upper Tu¬ronian after the carbonate sedimentation retrieval, represented by Moncharmontia apennini¬ca and Pseudocyclammina spharoidea species together with the “legacy” forms from Cenoma¬nian age; then also appear more complex genus as Eofallotia. 4) It seems like in both areas the Global Community Maduration Cycle of upper Cretaceous began simultaneously. However, from the middle-upper some sort of provincialism is noticeable with the presence of Scando¬nea and Reticulinella genus in the central Tethys, while the firth forms of meandropsinids are showns up for the Pyrenean realm, such paleoprovincialism considerably emphasizes during the latter stages of upper Cretaceous GCMC.
Cheng, Jie. "Paleoenvironmental Reconstruction of Florida Bay, South Florida, Using Benthic Foraminifera." FIU Digital Commons, 2009. http://digitalcommons.fiu.edu/etd/179.
Full textToomey, Heidi M. "Chlorophyll Fluorescence and Thermal Stress in Archaias angulatus (Class Foraminifera)." Thesis, University of South Florida, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=1549223.
Full textBenthic foraminifers that host algal symbionts are similar to corals in that they rely on their algal endosymbionts for their energy needs, calcify prolifically, and are sensitive to changes in environmental conditions. They are abundant in the benthos of coastal coral-reef areas and are found throughout the tropical and subtropical regions. Pulse Amplitude Modulated (PAM) chlorophyll fluorometry and chlorophyll a extraction techniques were used to quantify and compare the photosynthetic responses of the benthic foraminifera, Archaias angulatus and their isolated endosymbionts, Chlamydomonas hedleyi, to short-term changes in temperature. Maximum quantum efficiency (Fv/Fm) and rapid light curves (RLCs), from which relative electron transport rates (rETR) of photosystem II (PSII) were derived, were investigated over a thermal range from 4.4° to 33.9 °C in three experiments that were 7 to 31 days in duration. Typical mean yields (Fv/Fm) for healthy holobionts (symbionts in hospite) were 0.6 - 0.7, and for isolated symbionts 0.5 - 0.6. Chronic photoinhibition, indicated by significant decreases in Fv/Fm, occurred at temperatures above 31.0°C; there was minimal reduction in efficiency in cooler treatments. The trends between holobiont and symbionts were very similar in all of the photophysiological parameters measured [yield, photoefficiency (á), ETRmax and minimum saturating irradiance (Ek)] and supported the temperature range findings in terms of the tolerance of the specimens in the low temperatures up to 31.0 °C. For all photochemical measurements assessed, the holobiont values tended to be somewhat higher than those for the symbionts, with the exception of Ek, possibly indicating a tight coupling in the host-symbiont response during photosynthesis. Chlorophyll a (ìg/foram) was negatively correlated with temperature (r = -0.37, p < 0.001) in Experiments 1 and 2. However, in all 3 experiments, chlorophyll a was variable, suggesting a high degree of individual variability in A. angulatus and the ability to acclimate. Some differences observed among treatments may be related to differences in seasons when the specimens were collected and in length of time in culture prior to experiments. Holobiont median rETR light curve trends and photophysiological derived parameters recorded median Ek ranges of ~100-150 ìmol photons m-2 s-1, observed ETRmax light intensities of ~200 ìmol photons m-2 s-1 and photoinhibition, induced by increasing irradiance intensities, which occurred > 500 ìmol photons m-2 s-1. These light curve trends and derived parameters generally supported previous photosynthesis O2 and CO2 gas production studies of A. angulatus. The differences in responses associated with acclimation should be considered in design of future experimental studies. This was the first known physiological study of the viable temperature range and photobiology of A. angulatus using chlorophyll fluorometry methods. Though commonly found in Caribbean and Atlantic waters ranging from 14.0 – 31.0 °C, these results indicate a wider thermal-tolerance range for A. angulatus than was previously known.
Rae, James W. B. "Boron isotopes in benthic foraminifera : measurement, calibration and glacial CO2." Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.544334.
Full textRoss, Benjamin James. "Responses to Chemical Exposure by Foraminifera: Distinguishing Dormancy From Mortality." Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4397.
Full textDagher, Marcelle Bou. "Lower Eocene shelf smaller foraminifera a comparative inter-regional study." Thesis, University College London (University of London), 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.260930.
Full textHathorne, Edmund Charles. "The trace element and lithium isotope composition of planktonic foraminifera." Thesis, Open University, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.417477.
Full textBates, Stephanie. "Barium uptake by foraminifera : understanding past and present ocean processes." Thesis, University of Bristol, 2016. http://hdl.handle.net/1983/c12eed98-50c4-421f-8a79-af2f292fa971.
Full textAustin, Heather Anne. "The biology and ecology of benthic foraminifera inhabiting intertidal mudflats." Thesis, University of St Andrews, 2003. http://hdl.handle.net/10023/7099.
Full textOluyemi, Aturamu Adeyinka. "The palaeontology of Bering Sea foraminifera from the Late Quaternary." Thesis, University of Leicester, 2015. http://hdl.handle.net/2381/33161.
Full textBeer, Christopher James. "Planktic foraminifera, ocean sediments and the palaeo-marine carbonate system." Thesis, University of Southampton, 2010. https://eprints.soton.ac.uk/208361/.
Full textIshman, Scott E. "Quantitative analysis of Antarctic benthic foraminifera : application to paleoenvironmental interpretations /." The Ohio State University, 1990. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487683049375259.
Full textSchmuker, Barbara. "Recent planktic foraminifera in the Caribbean sea : distribution, ecology and taphonomy /." [S.l.] : [s.n.], 2000. http://e-collection.ethbib.ethz.ch/show?type=diss&nr=13559.
Full textMallon, Jürgen [Verfasser]. "Benthic Foraminifera of the Peruvian and Ecuadorian Continental Margin / Jürgen Mallon." Kiel : Universitätsbibliothek Kiel, 2012. http://d-nb.info/1020284048/34.
Full textLorenz, Andrea. "Variability of benthic foraminifera north and south of the Denmark Strait." [S.l.] : [s.n.], 2005. http://e-diss.uni-kiel.de/diss_1646/d1646.pdf.
Full textMarchitto, Thomas Mathew. "Zinc and cadmium in benthic foraminifera as tracers of ocean paleochemistry." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/55333.
Full textIncludes bibliographical references.
Benthic foraminiferal δ13C, Cd/Ca, and Ba/Ca are important tools for reconstructing nutrient distributions, and thus ocean circulation, on glacial-interglacial timescales. However, each tracer has its own "artifacts" that can complicate paleoceanographic interpretations. It is therefore advantageous to measure multiple nutrient proxies with the aim of separating the various complicating effects. Zn/Ca is introduced as an important aid toward this goal. Benthic (Hoeglundina elegans) Cd/Ca ratios from the Bahama Banks indicate that the North Atlantic subtropical gyre was greatly depleted in nutrients during the last glacial maximum (LGM). A high-resolution Cd/Ca record from 965 m water depth suggests that Glacial North Atlantic Intermediate Water formation was strong during the LGM, weakened during the deglaciation, and strengthened again during the Younger Dryas cold period. Comparison of Cd/Ca and δ13C data reveals apparent short-term changes in carbon isotopic air-sea signatures. Benthic foraminiferal Zn/Ca could be a sensitive paleoceanographic tracer because deep water masses have characteristic Zn concentrations that increase about ten-fold from the deep North Atlantic to the deep North Pacific. A "core top calibration" shows that Zn/Ca is controlled by bottom water dissolved Zn concentration and, like Cd/Ca and BalCa, by bottom water saturation state with respect to calcite Since Zn/Ca responds to a different range of saturation states than Cd/Ca, the two may be used together to evaluate changes in deep water carbonate ion (CO32- ) concentration. Zn/Ca and Cd/Ca ratios in the benthic foraminifer Cibicidoides wuellerstorfi exhibit large fluctuations over the past 100,000 years in a deep (3851 m) eastern equatorial Pacific sediment core. The data imply that bottom water CO32- concentrations were lowest during glacial Marine Isotope Stage 4 and highest during the last deglaciation. LGM CO32- concentrations appear to have been within a few μmol kg-1 of modern values. Deep North Atlantic Cd/Ca ratios imply much higher nutrient concentrations during the LGM. Although such data have usually been explained by a northward penetration of Southern Ocean Water (SOW), it has been suggested that they could result from increased preformed nutrient levels in the high-latitude North Atlantic or by increased aging of lower North Atlantic Deep Water (NADW). Glacial Zn/Ca data, however, require a substantially increased mixing with SOW and thus a reduction in NADW formation. Large changes in carbon isotopic air-sea exchange are invoked to reconcile benthic δ13C and trace metal data.
by Thomas Mathew Marchitto, Jr.
Ph.D.
Cotton, Laura. "Paleogene larger benthic foraminifera of Tanzania and the Eocene-Oligocene Transition." Thesis, Cardiff University, 2012. http://orca.cf.ac.uk/42726/.
Full textBergh, Eugene. "Neogene to quaternary foraminifera from the western margin of southern Africa." Doctoral thesis, Faculty of Science, 2019. http://hdl.handle.net/11427/30436.
Full textOzarko, Diana (Diana Lee) 1968 Carleton University Dissertation Earth Sciences. "Marsh foraminifera from Nanaimo, British Columbia: infaunal habitat and taphonomic implications." Ottawa.:, 1995.
Find full textEberwein, Astrid. "Holocene and Last Glacial Maximum (paleo-)productivity off Morroco : evidence from benthic foraminifera and stable carbon isotopes = (Paläo-)produktivität im Holozän und Letzten Glazialen Maximum vor Marokko erschlossen aus benthischen Foraminiferen und stabilen Kohlenstoffisotopen /." Bremerhaven : Alfred-Wegener-Institut für Polar- und Meeresforschung, 2007. http://www.loc.gov/catdir/toc/fy0712/2007425451.html.
Full text