9 results on '"Schmidt, Daniela"'
Search Results
2. Radiolarians Decreased Silicification as an Evolutionary Response to Reduced Cenozoic Ocean Silica Availability
- Author
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Lazarus, David B., Kotrc, Benjamin, Wulf, Gerwin, Schmidt, Daniela N., and Stanley, Steven M.
- Published
- 2009
- Full Text
- View/download PDF
3. Morphological Evolution, Ecological Diversification and Climate Change in Rodents
- Author
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Renaud, Sabrina, Michaux, Jacques, Schmidt, Daniela N., Aguilar, Jean-Pierre, Mein, Pierre, and Auffray, Jean-Christophe
- Published
- 2005
- Full Text
- View/download PDF
4. Linking evolution and development: Synchrotron Radiation X-ray tomographic microscopy of planktic foraminifers
- Author
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Schmidt, Daniela N, Rayfield, Emily J, Cocking, Alexandra, Marone, Federica, University of Zurich, and Schmidt, Daniela N
- Subjects
170 Ethics ,1911 Paleontology ,1105 Ecology, Evolution, Behavior and Systematics ,X-ray tomographic miscroscopy ,synchrotron radiation ,evolution ,610 Medicine & health ,10237 Institute of Biomedical Engineering ,planktic foraminifers ,development - Published
- 2012
5. The future of the northeast Atlantic benthic flora in a high CO2 world
- Author
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Brodie, Juliet, Williamson, Christopher J., Smale, Dan A., Kamenos, Nicholas A., Mieszkowska, Nova, Santos, Rui, Cunliffe, Michael, Steinke, Michael, Yesson, Christopher, Anderson, Kathryn M., Asnaghi, Valentina, Brownlee, Colin, Burdett, Heidi L., Burrows, Michael T., Collins, Sinead, Donohue, Penelope J.C., Harvey, Ben, Foggo, Andrew, Noisette, Fanny, Nunes, Joana, Ragazzola, Federica, Raven, John A., Schmidt, Daniela N., Suggett, David, Teichberg, Mirta, Hall-Spencer, Jason M., Department of Life Sciences, The Natural History Museum [London] (NHM), School of Earth and Ocean Sciences [Cardiff], Cardiff University, Marine Biological Association of the UK, The Laboratory, National Oceanography Centre [Southampton] (NOC), University of Southampton, School of Geographical and Earth Sciences, University of Glasgow, Marine Plant Ecology Research Group (ALGAE), Centre of Marine Sciences [Faro] (CCMAR), University of Algarve [Portugal]-University of Algarve [Portugal], School of Biological Sciences [Colchester], University of Essex, Institute of Zoology, Zoological Society of London, Department of Zoology (The University of British Columbia), University of British Columbia (UBC), Department of Earth, Environmental and Life Sciences (DISTAV), Universita degli studi di Genova, Marine Biological Association, Scottish Oceans Institute, University of St Andrews [Scotland], School of Earth and Environmental Sciences [University St Andrews], Scottish Marine Institute, Institute of Evolutionary Biology, University of Edinburgh, Marine Biology and Ecology Research Centre, Plymouth University, Ecogéochimie et Fonctionnement des Ecosystèmes Benthiques (EFEB), Adaptation et diversité en milieu marin (AD2M), Station biologique de Roscoff [Roscoff] (SBR), Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Station biologique de Roscoff [Roscoff] (SBR), Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Plymouth Marine Laboratory (PML), Plymouth Marine Laboratory, School of Earth Sciences [Bristol], University of Bristol [Bristol], Plant Functional Biology and Climate Change Cluster (C3), University of Technology Sydney (UTS), Division of Plant Sciences, University of Dundee, Leibniz-Zentrum für Marine Tropenökologie, UK Ocean Acidification Research Programme - NERC, UK Ocean Acidification Research Programme - Defra, UK Ocean Acidification Research Programme - DECC, NERC OARP [NE/H016996/1], University of St Andrews. Earth and Environmental Sciences, and Università degli studi di Genova = University of Genoa (UniGe)
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macroalgae ,Calcified algae ,Climate Research ,microphytobenthos ,Evolution ,QH301 Biology ,[SDV]Life Sciences [q-bio] ,Seagrasses ,Growth ,Review ,Ecosystems ,Klimatforskning ,invasive species ,QH301 ,Macroalgae ,SDG 13 - Climate Action ,Climate change ,SDG 14 - Life Below Water ,volatile gases ,Climate-change ,Biology ,Ekologi ,Ecology ,Invasive species ,Ocean acidification ,fungi ,Microphytobenthos ,Temperature ,Geokemi ,Coralline Algae ,Carbon ,Geochemistry ,Volatile gases ,Kelp ,climate change ,seagrasses ,[SDE]Environmental Sciences - Abstract
Seaweed and seagrass communities in the northeast Atlantic have been profoundly impacted by humans, and the rate of change is accelerating rapidly due to runaway CO2 emissions and mounting pressures on coastlines associated with human population growth and increased consumption of finite resources. Here, we predict how rapid warming and acidification are likely to affect benthic flora and coastal ecosystems of the northeast Atlantic in this century, based on global evidence from the literature as interpreted by the collective knowledge of the authorship. We predict that warming will kill off kelp forests in the south and that ocean acidification will remove maerl habitat in the north. Seagrasses will proliferate, and associated epiphytes switch from calcified algae to diatoms and filamentous species. Invasive species will thrive in niches liberated by loss of native species and spread via exponential development of artificial marine structures. Combined impacts of seawater warming, ocean acidification, and increased storminess may replace structurally diverse seaweed canopies, with associated calcified and noncalcified flora, with simple habitats dominated by noncalcified, turf-forming seaweeds. In this study, predictions are made as to how rapid warming and ocean acidification are likely to affect benthic flora and coastal ecosystems of the north-east Atlantic in this century based on global evidence from the literature as interpreted by the collective knowledge of the authorship. We predict that kelp forests will die out in the south due to warming, maerl habitat lost in the north through acidification, seagrasses will proliferate, associated epiphytes will switch from calcified algae to diatoms and filamentous species, and invasive species will thrive. Thus, structurally diverse seaweed canopies with associated calcified and noncalcified flora may be replaced with simple habitats dominated by noncalcified, turf-forming seaweeds. © 2014 The Authors.
- Published
- 2014
6. Linking evolution and development: Synchrotron Radiation X-ray tomographic microscopy of planktic foraminifers.
- Author
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SCHMIDT, DANIELA N., RAYFIELD, EMILY J., COCKING, ALEXANDRA, and MARONE, FEDERICA
- Subjects
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FORAMINIFERA , *BIOLOGICAL evolution , *DEVELOPMENTAL biology , *TOMOGRAPHY , *ONTOGENY , *PHYLOGENY , *MICROPALEONTOLOGY - Abstract
Making the link between evolutionary processes and development in extinct organisms is usually hampered by the lack of preservation of ontogenetic stages in the fossil record. Planktic foraminifers, which grow by adding chambers, are an ideal target organism for such studies as their test incorporates all prior developmental stages. Previously, studies of development in these organisms were limited by the small size of their early chambers. Here, we describe the application of synchrotron radiation X-ray tomographic microscopy (SRXTM) to document the ontogenetic history of the foraminifers Globigerinoides sacculifer and Globorotalia menardii. Our SRXTM scans permit resolution at submicrometre scale, thereby displaying additional internal structures such as pores, dissolution patterns and complexity of the wall growth. Our methods provide a powerful tool to pick apart the developmental history of these microfossils and subsequently assist in inferring phylogenetic relationships and evolutionary processes. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
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7. Biogeography and evolution of body size in marine plankton
- Author
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Schmidt, Daniela N., Lazarus, David, Young, Jeremy R., and Kucera, Michal
- Subjects
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MARINE plankton , *MARINE organisms , *PLANKTON , *AQUATIC biology - Abstract
Abstract: Body size is a central feature of any organism, reflecting its physiology, ecology and evolutionary history. Marine microplankton are major contributors to the particulate inorganic carbonate (foraminifers and coccolithophorids) and opal flux (radiolaria and diatoms) in the ocean and, hence, size changes in these organisms can influence global biogeochemical cycles. This paper is discussing abiotic influences on micro- and macroecological size changes among major marine plankton groups, linking these to evolutionary size changes during the Neogene. We review the patterns and outline the causes of size changes geographically and through time in coccolithophorids, foraminifers and radiolarians. The main feature of the Neogene size record is a dramatic size increase in foraminifers, a similarly dramatic reduction in the size range of coccolithophorids and highly variable size patterns in radiolarians. We argue that the observed pattern is too complex to be explained by a simple common forcing and propose that speculations on the response of oceanic biomineralisation to global warming have to consider the scales at which marine plankton evolve. [Copyright &y& Elsevier]
- Published
- 2006
- Full Text
- View/download PDF
8. The evolutionary history of size variation of planktic foraminiferal assemblages in the Cenozoic
- Author
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Schmidt, Daniela N., Thierstein, Hans R., and Bollmann, J.
- Subjects
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CLIMATE change , *NEOGENE paleoclimatology , *RADIATION , *GEOGRAPHY - Abstract
The iterative evolutionary radiation of planktic foraminifers is a well-documented macroevolutionary process. Here we document the accompanying size changes in entire planktic foraminiferal assemblages for the past 70 My and their relationship to paleoenvironmental changes. After the size decrease at the Cretaceous/Paleogene (K/P) boundary, high latitude assemblages remained consistently small. Size evolution in low latitudes can be divided into three major phases: the first is characterized by dwarfs (65–42 Ma), the second shows moderate size fluctuations (42–14 Ma), and in the third phase, planktic foraminifers have grown to the unprecedented sizes observed today.Our analyses of size variability with paleoproxy records indicate that periods of size increase coincided with phases of global cooling (Eocene and Neogene). These periods were characterized by enhanced latitudinal and vertical temperature gradients in the oceans and high diversity (polytaxy). In the Paleocene and during the Oligocene, the observed (minor) size changes of the largely low-diversity (oligotaxic) assemblages seem to correlate with productivity changes. However, polytaxy per se was not responsible for larger test sizes. [Copyright &y& Elsevier]
- Published
- 2004
- Full Text
- View/download PDF
9. Habitat tracking as a response of the planktic foraminifer Globorotalia truncatulinoides to environmental fluctuations during the last 140 kyr
- Author
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Renaud, Sabrina and Schmidt, Daniela N.
- Subjects
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FOSSIL globorotalia , *HABITATS - Abstract
Morphological variability of the planktic foraminifer Globorotalia truncatulinoides, estimated by size, shape, and coiling direction of the test, has been studied throughout the last 140 kyr in three cores in the South Atlantic. The biogeographic component of the morphological variation has been identified as difference between the three cores, located in the subantarctic frontal system, the equatorial upwelling zone, and the northern margin of the subtropical gyre. Temporal variability of morphology has been quantified and compared to biogeographic morphological variations, and paleoenvironmental proxies. The most important morphological differentiation is related to biogeography. Size and shape vary according to a temperature gradient across the different cores. This pattern is likely the result of differences between the four cryptic genetic species that have been previously identified within the taxon, and that are associated with different ecological preferences. Temporal variations can be recognized within each of the three cores, even in the most stable situation of the subtropical gyre. Significant correlations emerge between morphology and paleoenvironmental proxies, suggesting that the morphological variations are a response to environmental change. The same shape–temperature relationship emerges from both, biogeographic differences and local temporal variations. This suggests that the complex of species G. truncatulinoides mainly reacted to the glacial–interglacial climatic fluctuations of the last 140 kyr by a process of habitat tracking, i.e. the different species shifted their geographic distribution without major modifications of their ecological preferences. Yet, evolution may be involved as a response to environmental changes on a longer time scale. [Copyright &y& Elsevier]
- Published
- 2003
- Full Text
- View/download PDF
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