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  • 1
    Publication Date: 2023-06-27
    Keywords: 27-263; Deep Sea Drilling Project; DEPTH, sediment/rock; DRILL; Drilling/drill rig; DSDP; DSDP/ODP/IODP sample designation; Glomar Challenger; Indian Ocean//PLAIN; Leg27; Mass spectrometer Finnigan Delta Plus; Sample code/label; δ13C, organic carbon
    Type: Dataset
    Format: text/tab-separated-values, 60 data points
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  • 2
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    PANGAEA
    In:  Supplement to: Oosting, A M; Leereveld, H; Dickens, Gerald Roy; Henderson, R A; Brinkhuis, Henk (2006): Correlation of Barremian-Aptian (mid-Cretaceous) dinoflagellate cyst assemblages between the Tethyan and Austral realms. Cretaceous Research, 27(6), 792-813, https://doi.org/10.1016/j.cretres.2006.03.012
    Publication Date: 2023-06-27
    Description: Quantified organic-walled dinoflagellate cyst (dinocyst) assemblages are presented for two sedimentary successions deposited in neritic environments of the Tethys Ocean during the Barremian and Aptian in an attempt to reconcile established dinocyst biostratigraphic schemes for Tethyan and Austral regions. One section is at Angles, southeast France (the Barremian stratotype section); the other is at Deep Sea Drilling Project Site 263, off northwest Australia. We also construct a carbon isotope record for Site 263 using bulk organic carbon. Both sections contain abundant, well-preserved dinocyst assemblages. These are diverse, with 89 taxa identified at Angles and 103 taxa identified at Site 263. Of these, more than 93% are cosmopolitan. When combined with other work at Angles and Site 263, we found that nine dinocysts have their first occurrence (FO) or last occurrence (LO) at both locations. These dinocyst events are, in alphabetical order: LO of Cassiculosphaeridia magna, FO of Criboperidinium? tenuiceras, LO of Kleithriasphaeridium fasciatum, LO of Muderongia staurota, FO of Odontochitina operculata, LO of Phoberocysta neocomica, FO of Prolixosphaeridium parvispinum, FO of Pseudoceratium retusum var. securigerum, and FO of Tehamadinium sousense. Although these events support a Barremian-Aptian age for both sections, their stratigraphic order is not the same in the sections. The d13Corg record at Site 263 displays a characteristic series of changes that have also been recorded in other carbon isotope curves spanning the Late Barremian-Early Aptian. Such independent dating (along with ammonite zones at Angles) suggests that three of the nine dinocyst events are approximately isochronous at Angles and Site 263: the LO of K. fasciatum in the mid Barremian, the FO of P. retusum var. securigerum and the FO of C.? tenuiceras in the earliest Aptian; the other six dinocyst events are diachronous. Dinocyst assemblages at Site 263 can be loosely placed within existing Australian zonation schemes, providing much-needed calibration. Our data suggest that the Muderongia testudinaria Zone ends in sediments of mid Barremian age, the succeeding Muderongia australis Zone extends into the Early Aptian, and the younger Odontochitina operculata Zone begins in Early Aptian deposits. The boundary between the M. australis and O. operculata zones, and the Ovoidinium cinctum (as Ascodinium) Subzone, positioned at the top of the M. australis Zone when present, could not be recognized incontrovertibly. Interestingly, however, this horizon broadly correlates with the onset and extent of the Selli Event, a time of major biogeochemical change.
    Keywords: 27-263; Angles; Deep Sea Drilling Project; DRILL; Drilling/drill rig; DSDP; France; Glomar Challenger; HAND; Indian Ocean//PLAIN; Leg27; Sampling by hand
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 3
    Publication Date: 2023-07-10
    Keywords: 27-263; Achomosphaera spp.; Adnatosphaeridium tutulosum; Alterbidinium spp.; Aprobolocysta eilema; Aprobolocysta sp.; Aprobolocysta spp.; Apteodinium granulatum; Apteodinium maculatum; Apteodinium sp.; Avellodinium lepidum; Batiacasphaera reticulata; Batiacasphaera spp.; Batioladinium jaegeri; Batioladinium micropodum; Batioladinium spp.; Belodinium dysculum; Canningia reticulata; Carpodinium granulatum; Carpodinium spp.; Cassiculosphaeridia magna; Cassiculosphaeridia pygmaeus; Cassiculosphaeridia spp.; Cerbia cf. tabulata; Cernicysta helbyi; Cernicysta sp.; Cernicysta spp.; Circulodinium colliveri; Circulodinium spp.; Circulodinium vermiculatum; Cleistosphaeridium spp.; Cometodinium spp.; Coronifera oceanica; Cribroperidinium sp.; Cribroperidinium spp.; Cribroperidinium tenuiceras; Cyclonephelium spp.; Deep Sea Drilling Project; DEPTH, sediment/rock; Diconodinium micropunctatum; Dingodinium cerviculum; Discorsia nannus; DRILL; Drilling/drill rig; Druggidium deflandrei; DSDP; DSDP/ODP/IODP sample designation; Endoscrinium attadalense; Endoscrinium bessebae; Endoscrinium spp.; Epitricysta vinckensis; Escharisphaeridea spp.; Exochosphaeridium spp.; Florentinia resex; Florentinia spp.; Fromea monilifera; Glomar Challenger; Gonyaulacysta spp.; Herendeenia postprojecta; Heslertonia spp.; Heterosphaeridium heteracanthum; Heterosphaeridium spp.; Hystrichodinium pulchrum; Hystrichodinium spp.; Impagidinium phlyctaena; Impagidinium spp.; Indian Ocean//PLAIN; Kaiwaradinium scrutillinum; Kiokansium unituberculatum; Kleithriasphaeridium eoinodes; Leg27; Leiosphaera spp.; Leptodinium spp.; Lithodinia spp.; Meiourogonyaulax psora; Meiourogonyaulax sp.; Microdinium spp.; Muderongia australis; Muderongia crusis; Muderongia mcwhaei; Muderongia staurota; Muderongia tetracantha; Odontochitina operculata; Oligosphaeridium complex; Ovoidinium cinctum; Pareodinia ceratophora; Pareodinia spp.; Pentafidia punctata; Pervosphaeridium truncatum; Platycistidia eisenackii; Prolioxosphaeridium parvispinium; Prolixosphaeridium spp.; Protoellipsodinium spinosum; Protoellipsodinium spp.; Pseudoceratium retusum var. securigerum; Pterodinium spp.; Pyxidiella tumida; Rhombodella natans; Sample code/label; Scriniodinium campanula; Sentusidinium spp.; Sepispinula ambigua; Sepispinula spp.; Spiniferites spp.; Stiphrosphaeridium anthophorum; Stiphrosphaeridium dictyophorum; Subtilisphaera spp.; Systematophora areolata; Tanyosphaeridium spp.; Tehamadinium sousense; Tenua spp.; Tetrachacysta allenii; Trichodinium castanea; Wallodinium luna
    Type: Dataset
    Format: text/tab-separated-values, 1456 data points
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  • 4
    Publication Date: 2023-07-10
    Keywords: Acanthaulax spp.; Achomosphaera spp.; Angles; Batioladinium micropodum; Callaiosphaeridium asymmetricum; Canningia spp.; Cassiculosphaeridia magna; Cassiculosphaeridia reticulata; Cerbia tabulata; Chytroeisphaeridia chytroeides; Circulodinium spp.; Cleistosphaeridium spp.; Cometodinium comatum; Cometodinium habibii; Coronifera albertii; Coronifera oceanica; Cribroperidinium spp.; Cribroperidinium tenuiceras; Ctenidodinium elegantulum; Cyclonephelium intonsum; Cymososphaeridium validum; Dingodinium cerviculum; Dingodinium europaeum; Discorsia nannus; Dissiliodinium globulum; Druggidium apicopaucicum; Druggidium deflandrei; Elytrocysta circulata; Endoscrinium bessebae; Escharisphaeridia spp.; Exiguisphaera phragma; Exochosphaeridium phragmites; Florentinia cooksoniae; Florentinia interrupta; Florentinia mantellii; Florentinia spp.; France; Gardodinium spp.; Gardodinium trabeculosum; HAND; Heslertonia heslertonensis; Heterosphaeridium heteracanthum; Histiocysta outananensis; Hystrichodinium pulchrum; Hystrichogonyaulax spp.; Hystrichosphaeridium recurvatum; Hystrichsphaeridium tubiferum; Kiokansium spp.; Kleithriasphaeridium corrugatum; Kleithriasphaeridium eoinodes; Meiourogonyaulax amlasis; Meiourogonyaulax stoveri; Muderongia simplex; Muderongia staurota; Occisucysta tentoria; Odontochitina operculata; Oligosphaeridium complex; Ovoidinium diversum; Palaeoperidinium cretaceum; Pareodinia ceratophora; Phoberocysta neocomica; Phoberocysta tabulata; Polystephanephorus euryanthus; Prolixosphaeridium parvispinum; Prolixosphaeridium spp.; Protoellipsodinium spp.; Protoellipsodinium touile; Pseudoceratium pelliferum; Pseudoceratium retusum; Pseudoceratium retusum var. securigerum; Pterodinium spp.; Rhynchodiniopsis fimbriata; Sample code/label; Sampling by hand; Scriniodinium campanula; Sentusidinium spp.; Sepispinula spp.; Spiniferites spp.; Stanfordella cretacea; Stiphrosphaeridium dictyophorum; Subtilisphaera spp.; Systematophora spp.; Tanyosphaeridium spp.; Tehamadinium coummia; Tehamadinium sousense; Trichodinium castanea; Trichodinium ciliatum; Wallodinium krutzschii; Wrevittia cassidata; Wrevittia helicoidea; Wrevittia perforobtusa
    Type: Dataset
    Format: text/tab-separated-values, 1800 data points
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 207 (1965), S. 1286-1287 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The section of Kaiti consists of rhythmically bedded graded sandstone and mudstone, interpreted to have been deposited largely by turbidity currents. Convoluted laminae are present in most of the sandstone beds. Individual beds containing convolutions are of uniform thickness throughout their ...
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1525-1314
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: Abstract Regional metamorphic rocks that form Late Palaeozoic subduction complexes in central Queensland, Australia, are products of two metamorphic episodes. Synaccretion metamorphism (M1) gave rise to prehnite-pumpellyite and greenschist facies rocks, whereas a subsequent episode (M2) at about 250 Ma formed upper greenschist to upper amphibolite facies rocks of both intermediate- and low-pressure type, probably in a compressive arc or back-arc setting. A similar pattern can be recognized for 1000 km along the New England Fold Belt, although at several localities, where higher grade rocks are exposed, metamorphism was essentially continuous over the M1-M2 interval, with a rapid rise in geothermal gradient at the end of accretion. Where out-stepping of tectonic elements has occurred at long-lived convergent margins elsewhere, similar overprinting of high- by lower-pressure facies series is anticipated, complicating the tectonic interpretation of metamorphism. The discrete character of metamorphic events may be blurred where conditions giving rise to a major episode of accretion and out-stepping are followed by the subduction of a major heat source.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The isotope260Lr, produced in reactions of18O with249Bk, was used to perform chemical experiments on lawrencium to learn more about its chemical properties. These experiments involved extractions with thenoyl trifluoroacetate, elutions from cation exchange resin columns with ammonium alpha-hydroxyisobutyrate, and reverse-phase chromatography using hydrogen di(2-ethylhexyl) orthophosphoric acid to investigate the chemical properties of Lr. The results from the elutions gave information about the ionic radius of Lr(III) which was found to elute very close to Er. An attempt to reduce Lr(III) with hydroxylamine hydrochloride was unsuccessful.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 202 (1964), S. 886-888 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] LAKE BONNEY is shown to be a natural example of j the trapping and storing of solar energy by a saltwater density gradient. Enough light passes through the 12-ft.-thick ice cover during the short Antarctic summer to maintain maximum temperatures of 7 C and 1-3 C in the eastern and western lobes ...
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0975
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences
    Notes: Abstract The nature and interpretation of the fossil record of Acanthaster planci from the GBR is reviewed in the light of comments from Keesing et al. (1992) and Pandolfi (1992). Skeletal remains of A. planci in reef-top sediment of many reefs has been derived from very large numbers of individuals, indicating substantial, long-term mortality at reef-top locations. The fossil record provides useful perspective on mortality patterns in the absence of substantive ecological data. The incidence of skeletal elements on reefs where they are abundant cannot be adequately accounted for by the mortality of non-outbreak populations as estimated by recent surveys. Analysis of all available data reaffirms a relationship between the incidence of skeletal elements in surface sediment and observed outbreak history. There is no presently identified taphonomic mechanism by which the accumulation of A. planci skeletal elements released on death might be systematically biased relative to other skeletal components of reefal sediment. Because of skeletal degradation, physical transport and extensive bioturbation that applies in shallow-water reefal sediment, reconstructive taphonomic analysis of A. planci skeletal remains is not achievable. Core sediment, on which interpretation of the longterm fossil record of A. planci is based, is homogeneous, unstratified, and has experienced substantial time averaging due to pervasive bioturbation. Extensive bulk sediment dating has shown that the cores have retained a general age structure but fine-scale stratigraphic detail, required for the recognition of outbreak events from the fossil record available in reefal sediment is unlikely. As required by the principle of simplicity, the proposition that abundant A. planci skeletal elements found in sediment from Green Island, John Brewer and other reefs of the GBR represent the time-averaged product of outbreaking populations should be adopted as the favoured working hypothesis. Other alternative explantions have been advanced but all require patterns or processes that have yet to be substantiated.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Coral reefs 11 (1992), S. 103-108 
    ISSN: 1432-0975
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences
    Notes: Abstract A total of 1655 crown-of-thorns starfish skeletal elements were recovered from 237 surface sediment samples from Davies, Centipede, Myrmidon, Hope, Holbourne Island, 22–110, Gannet Cay and Lady Musgrave Island Reefs of the central and southern sectors of the Great Barrier Reef. Three categories of reef may be recognised on the incidence of Acanthaster planci skeletal elements in surface sediment from these and previously studied reefs: category A (abundant, 〉12 elements kg1-), category C (common, 3–8 elements kg-1) and category C (rare, 0–0.1 elements kg-1). These categories parallel estimates of crown-of-thorns populations in the period 1986–1990. “A” reefs have generally experienced high intensity outbreaks, “C” reefs less intense or perhaps less frequent outbreaks and “R” reefs have had little or no crown-of-thorns presence. The incidence of crown-of-thorns skeletal elements in surface sediment potentially provides an indication of population densities and outbreaks over a time scale of several decades. A perspective of contemporary crown-of-thorns incidence on the many reefs of the GBR lacking direct observational records may thereby be obtained. For Holbourne Island a comparison was made of element incidence in an area of known mass mortality induced by poisoning with a control area that was undisturbed. The incidence of A. planci skeletal elements is comparable in the two areas and similar to the incidence established for other reefs such as Green Island and John Brewer where high intensity outbreaks are known to have occurred. A direct relationship between high incidence of elements in surface sediment and mass mortality following outbreak events is indicated.
    Type of Medium: Electronic Resource
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