133 research outputs found

    Mg/Ca-Temperature Calibration of Polar Benthic foraminifera species for reconstruction of bottom water temperatures on the Antarctic shelf

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    Benthic foraminifera Mg/Ca is a well-established bottom water temperature (BWT) proxy used in paleoclimate studies. The relationship between Mg/Ca and BWT for numerous species has been determined using core-top and culturing studies. However, the scarcity of calcareous microfossils in Antarctic shelf sediments and poorly defined calibrations at low temperatures has limited the use of the foraminiferal Mg/Ca paleothermometer in ice proximal Antarctic sediments. Here we present paired ocean temperature and modern benthic foraminifera Mg/Ca data for three species, Trifarina angulosa, Bulimina aculeata, and Globocassidulina subglobosa, but with a particular focus on Trifarina angulosa. The core-top data from several Antarctic sectors span a BWT range of −1.7 to +1.2 °C and constrain the relationship between Mg/Ca and cold temperatures. We compare our results to published lower-latitude core-top data for species in the same or related genera, and in the case of Trifarina angulosa, produce a regional calibration. The resulting regional equation for Trifarina angulosa is Temperature (°C) = (Mg/Ca −1.14 ± 0.035)/0.069 ± 0.033). Addition of our Trifarina angulosa data to the previously published Uvigerina spp. dataset provides an alternative global calibration, although some data points appear to be offset from this relationship and are discussed. Mg-temperature relationships for Bulimina aculeata and Globocassidulina subglobosa are also combined with previously published data to produce calibration equations of Temperature (°C) = (Mg/Ca-1.04 ± 0.07)/0.099 ± 0.01 and Temperature (°C) = (Mg/Ca-0.99 ± 0.03)/0.087 ± 0.01, respectively. These refined calibrations highlight the potential utility of benthic foraminifera Mg/Ca-paleothermometry for reconstructing past BWT in Antarctic margin settings

    Antarctic Environmental Change and Ice Sheet Evolution through the Miocene to Pliocene ¿ A perspective from the Ross Sea and George V to Wilkes Land Coasts

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    We wish to acknowledge the support of National Antarctic Programmes and the International Scientific Drilling Programmes and Projects that have allowed our community to acquire the critical records of environmental change that have been discussed in this review. We thank Jenny Black, GNS Science, for her assistance with Fig. 9.2. R.L., T.N., R.M., C.O. and N.G. acknowledge funding support from the New Zealand Ministry of Business and Innovation and Employment through the Antarctic Science Platform contract (ANTA1801) Antarctic Ice Dynamics Project (ASP-021-01). C.E. acknowledges funding by the Spanish Ministry of Economy, Industry and Competitivity (grant CTM2017-89711-C2-1/2-P), co-funded by the European Union through FEDER funds. L.F.P. was funded through the European Union’s Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement number 792773 for the West Antarctic Margin Signatures of Ice Sheet Evolution (WAMSISE) Project

    Cenozoic history of Antarctic glaciation and climate from onshore and offshore studies

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    The past three decades have seen a sustained and coordinated effort to refine the seismic stratigraphic framework of the Antarctic margin that has underpinned the development of numerous geological drilling expeditions from the continental shelf and beyond. Integration of these offshore drilling datasets covering the Cenozoic era with Antarctic inland datasets, provides important constraints that allow us to understand the role of Antarctic tectonics, the Southern Ocean biosphere, and Cenozoic ice sheet dynamics and ice sheet–ocean interactions on global climate as a whole. These constraints are critical for improving the accuracy and precision of future projections of Antarctic ice sheet behaviour and changes in Southern Ocean circulation. Many of the recent advances in this field can be attributed to the community-driven approach of the Scientific Committee on Antarctic Research (SCAR) Past Antarctic Ice Sheet Dynamics (PAIS) research programme and its two key subcommittees: Paleoclimate Records from the Antarctic Margin and Southern Ocean (PRAMSO) and Palaeotopographic-Palaeobathymetric Reconstructions. Since 2012, these two PAIS subcommittees provided the forum to initiate, promote, coordinate and study scientific research drilling around the Antarctic margin and the Southern Ocean. Here we review the seismic stratigraphic margin architecture, climatic and glacial history of the Antarctic continent following the break-up of Gondwanaland in the Cretaceous, with a focus on records obtained since the implementation of PRAMSO. We also provide a forward-looking approach for future drilling proposals in frontier locations critically relevant for assessing future Antarctic ice sheet, climatic and oceanic change.We thank many people who collaborated, by sharing data and ideas, on geoscience research projects under the umbrella of the highly successful Paleoclimate Records from the Antarctic Margin and Southern Ocean (PRAMSO) and Palaeotopographic-Palaeobathymetric Reconstructions subcommittees of the Scientific Committee on Antarctic Research (SCAR) Past Antarctic Ice Sheet scientific program. This synthesis, which reflects our views, would not have been possible without the efforts of these many investigators, most of whom continue their collaborative Antarctic studies, now under the successor SCAR INSTANT programme. Chris Sorlien is thanked for drafting Fig. 3.6. We thank John Anderson, Peter Barrett, Giuliano Brancolini and Alan Cooper for their useful comments and for their continuous dedication to the past Antarctic Ice Sheet evolution reconstructions. We thank Nigel Wardell, Frank Nitsche and Paolo Diviacco for maintaining the Seismic Data Library System and the National Antarctic funding agencies of many countries (Australia, China, Germany, Italy, Japan, Korea, New Zealand, Russia, Spain, the UK, the United States) for supporting geophysical and geological surveys essential for Paleotopographic and Paleobathymetric reconstructions. We thank the International Ocean Discovery Program (IODP) for its support of recent expeditions that arose out of PRAMSO discussions. R.M. was funded by the Royal Society Te Apārangi NZ Marsden Fund (grant 18-VUW-089). C.E. acknowledges funding by the Spanish Ministry of Economy, Industry and Competitivity (grants CTM2017-89711-C2-1/2-P), cofunded by the European Union through FEDER funds. L.D.S. and F.D. were funded by the Programma Nazionale delle Ricerche in Antartide (PNRA16_00016 project and PNRA 14_00119). R.Larter and C.D.H. were funded by the BAS Polar Science for Planet Earth Programme and NERC UK IODP grant NE/J006548/1. S.K. was supported by the KOPRI Grant (PE21050). L.P. was funded by the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 792773 WAMSISE. A.S. and S.G. were funded by NSF Office of Polar Programs (Grants OPP-1744970 (A.S.), -1143836 (A.S.), and -1143843 (S.G.). This is University of Texas Institute for Geophysics Contribution #3784. B.D. acknowledges funding from a Rutherford Foundation Postdoctoral Fellowship (RFT-VUW1804-PD). K.G. and G.K. were funded by AWI research programme Polar Regions and Coasts in the changing Earth System (PACES II) and the Sub-EIS-Obs programme by the Bundesanstalt für Geowissenschaften und Rohstoffe (BGR). RL, RM, TN acknowledge support from MBIE Antarctic Science Platform contract ANTA1801

    On the Origin and Trigger of the Notothenioid Adaptive Radiation

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    Adaptive radiation is usually triggered by ecological opportunity, arising through (i) the colonization of a new habitat by its progenitor; (ii) the extinction of competitors; or (iii) the emergence of an evolutionary key innovation in the ancestral lineage. Support for the key innovation hypothesis is scarce, however, even in textbook examples of adaptive radiation. Antifreeze glycoproteins (AFGPs) have been proposed as putative key innovation for the adaptive radiation of notothenioid fishes in the ice-cold waters of Antarctica. A crucial prerequisite for this assumption is the concurrence of the notothenioid radiation with the onset of Antarctic sea ice conditions. Here, we use a fossil-calibrated multi-marker phylogeny of nothothenioid and related acanthomorph fishes to date AFGP emergence and the notothenioid radiation. All time-constraints are cross-validated to assess their reliability resulting in six powerful calibration points. We find that the notothenioid radiation began near the Oligocene-Miocene transition, which coincides with the increasing presence of Antarctic sea ice. Divergence dates of notothenioids are thus consistent with the key innovation hypothesis of AFGP. Early notothenioid divergences are furthermore congruent with vicariant speciation and the breakup of Gondwana

    A large West Antarctic Ice Sheet explains early Neogene sea-level amplitude

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    Early to Middle Miocene sea-level oscillations of approximately 40-60 m estimated from far-field records1-3 are interpreted to reflect the loss of virtually all East Antarctic ice during peak warmth2. This contrasts with ice-sheet model experiments suggesting most terrestrial ice in East Antarctica was retained even during the warmest intervals of the Middle Miocene4,5. Data and model outputs can be reconciled if a large West Antarctic Ice Sheet (WAIS) existed and expanded across most of the outer continental shelf during the Early Miocene, accounting for maximum ice-sheet volumes. Here we provide the earliest geological evidence proving large WAIS expansions occurred during the Early Miocene (~17.72-17.40 Ma). Geochemical and petrographic data show glacimarine sediments recovered at International Ocean Discovery Program (IODP) Site U1521 in the central Ross Sea derive from West Antarctica, requiring the presence of a WAIS covering most of the Ross Sea continental shelf. Seismic, lithological and palynological data reveal the intermittent proximity of grounded ice to Site U1521. The erosion rate calculated from this sediment package greatly exceeds the long-term mean, implying rapid erosion of West Antarctica. This interval therefore captures a key step in the genesis of a marine-based WAIS and a tipping point in Antarctic ice-sheet evolution

    Climate-controlled submarine landslides on the Antarctic continental margin

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    Antarctica’s continental margins pose an unknown submarine landslide-generated tsunami risk to Southern Hemisphere populations and infrastructure. Understanding the factors driving slope failure is essential to assessing future geohazards. Here, we present a multidisciplinary study of a major submarine landslide complex along the eastern Ross Sea continental slope (Antarctica) that identifies preconditioning factors and failure mechanisms. Weak layers, identified beneath three submarine landslides, consist of distinct packages of interbedded Miocene- to Pliocene-age diatom oozes and glaciomarine diamicts. The observed lithological differences, which arise from glacial to interglacial variations in biological productivity, ice proximity, and ocean circulation, caused changes in sediment deposition that inherently preconditioned slope failure. These recurrent Antarctic submarine landslides were likely triggered by seismicity associated with glacioisostatic readjustment, leading to failure within the preconditioned weak layers. Ongoing climate warming and ice retreat may increase regional glacioisostatic seismicity, triggering Antarctic submarine landslides

    Radiation of Extant Cetaceans Driven by Restructuring of the Oceans

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    The remarkable fossil record of whales and dolphins (Cetacea) has made them an exemplar of macroevolution. Although their overall adaptive transition from terrestrial to fully aquatic organisms is well known, this is not true for the radiation of modern whales. Here, we explore the diversification of extant cetaceans by constructing a robust molecular phylogeny that includes 87 of 89 extant species. The phylogeny and divergence times are derived from nuclear and mitochondrial markers, calibrated with fossils. We find that the toothed whales are monophyletic, suggesting that echolocation evolved only once early in that lineage some 36–34 Ma. The rorqual family (Balaenopteridae) is restored with the exclusion of the gray whale, suggesting that gulp feeding evolved 18–16 Ma. Delphinida, comprising all living dolphins and porpoises other than the Ganges/Indus dolphins, originated about 26 Ma; it contains the taxonomically rich delphinids, which began diversifying less than 11 Ma. We tested 2 hypothesized drivers of the extant cetacean radiation by assessing the tempo of lineage accumulation through time. We find no support for a rapid burst of speciation early in the history of extant whales, contrasting with expectations of an adaptive radiation model. However, we do find support for increased diversification rates during periods of pronounced physical restructuring of the oceans. The results imply that paleogeographic and paleoceanographic changes, such as closure of major seaways, have influenced the dynamics of radiation in extant cetaceans

    Phylogenetic Relationships and Evolutionary Patterns of the Order Collodaria (Radiolaria)

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    Collodaria are the only group of Radiolaria that has a colonial lifestyle. This group is potentially the most important plankton in the oligotrophic ocean because of its large biomass and the high primary productivity associated with the numerous symbionts inside a cell or colony. The evolution of Collodaria could thus be related to the changes in paleo-productivity that have affected organic carbon fixation in the oligotrophic ocean. However, the fossil record of Collodaria is insufficient to trace their abundance through geological time, because most collodarians do not have silicified shells. Recently, molecular phylogeny based on nuclear small sub-unit ribosomal DNA (SSU rDNA) confirmed Collodaria to be one of five orders of Radiolaria, though the relationship among collodarians is still unresolved because of inadequate taxonomic sampling. Our phylogenetic analysis has revealed four novel collodarian sequences, on the basis of which collodarians can be divided into four clades that correspond to taxonomic grouping at the family level: Thalassicollidae, Collozoidae, Collosphaeridae, and Collophidae. Comparison of the results of our phylogenetic analyses with the morphological characteristics of each collodarian family suggests that the first ancestral collodarians had a solitary lifestyle and left no silica deposits. The timing of events estimated from molecular divergence calculations indicates that naked collodarian lineages first appeared around 45.6 million years (Ma) ago, coincident with the diversification of diatoms in the pelagic oceans. Colonial collodarians appeared after the formation of the present ocean circulation system and the development of oligotrophic conditions in the equatorial Pacific (ca. 33.4 Ma ago). The divergence of colonial collodarians probably caused a shift in the efficiency of primary production during this period
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