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  • Articles  (3,070,741)
  • 1985-1989  (1,185,261)
  • 1980-1984  (950,557)
  • 1970-1974  (692,018)
  • 1945-1949  (126,898)
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  • 1
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2014-08-15
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 2
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2014-08-13
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 3
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2014-08-19
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 4
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    Zeitschrift für Gletscherkunde und Glazialgeologie
    In:  EPIC3Innsbruck, Zeitschrift für Gletscherkunde und Glazialgeologie
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 5
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    Zeitschrift für Gletscherkunde und Glazialgeologie
    In:  EPIC3Innsbruck, Zeitschrift für Gletscherkunde und Glazialgeologie
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 6
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    Zeitschrift für Gletscherkunde und Glazialgeologie
    In:  EPIC3Innsbruck, Zeitschrift für Gletscherkunde und Glazialgeologie
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 7
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    Zeitschrift für Gletscherkunde und Glazialgeologie
    In:  EPIC3Innsbruck, Zeitschrift für Gletscherkunde und Glazialgeologie
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 8
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    Wiley
    In:  EPIC3The Ocean Floor : Bruce Heezen commemorative volume, (A Wiley-Interscience publication), Chichester, Wiley, pp. 147-163, ISBN: 0-471-10091-9
    Publication Date: 2014-05-12
    Description: The sedimentation regime off Northwest Africa is shaped by: (1) structur~al factors. which result in generallv low relief on land. shelf widths between 40 and more than 120 km. and av-erage sfope inclinations between 10 30' and 30; (2) land climates. which contral the delivery of terrigenous particles to the margin: (3) water movements including boundary currents and upwelling; and (4) the post- Pleistocene sea level rise. This chapter combines published and new results arising from research into the sedimentation processes off Northwest Africa. and emphasizes particularly the activities of the Kiel marine geological group during the past few years. Reviews of cruise activities and results were given in Closs et al. (1969) (Meteor cruise 8. 1967. off Morocco) . Seibold (1972) (Meteor cmise 25 . 1971. off Sahara to Central Senegal). Seibold and Hinz (1976) (Meteor cmise 39,1975 . and Valdivia cruise 10. 1975, from Morocco to South Senegal), and Waiden et al. (1974) (Meteor cmise 30, 1973, off Sierra Leone). Some of these cmises were used for pre- or post-site surveys for the Deep-Sea Drilling Project, or to add undisturbed Quaternary cores to the Glomar Challenger cores (leg 41, ] 975; Lancelot, et al .• 1978); leg 47 A, Arthur er al .• 1979; Lutze et al., 1979). We have concentrated our geological investigations on a number of standard profiles from the shelf to the upper continental rise as given in Figure 1. The manuscript was finished May 1979.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Inbook , peerRev
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  • 9
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    In:  EPIC3Neues Jahrbuch für Geologie und Paläontologie / Monatshefte, H 9, pp. 555-569, ISSN: 0028-3630
    Publication Date: 2014-05-14
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , peerRev
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  • 10
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 11
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 12
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 13
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 14
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
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  • 15
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 16
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 17
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 18
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 19
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 20
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
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  • 21
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
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  • 22
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 23
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    Colloques Internationaux du C.N.R.S.
    In:  EPIC3England, Colloques Internationaux du C.N.R.S.
    Publication Date: 2019-07-17
    Repository Name: EPIC Alfred Wegener Institut
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  • 24
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Communications and Media Relations, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2016-07-17
    Repository Name: EPIC Alfred Wegener Institut
    Type: Weekly Reports , notRev
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  • 25
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Alfred-Wegener-Institute for Polar- and Marine Research, Bremerhaven, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2016-07-16
    Repository Name: EPIC Alfred Wegener Institut
    Type: Weekly Reports , notRev
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  • 26
    Publication Date: 2017-09-18
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 27
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    Dating Laboratory, University of Helsinki
    In:  EPIC3Helsinki, Finland, Dating Laboratory, University of Helsinki
    Publication Date: 2019-09-03
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 28
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2020-06-12
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 29
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    Editions Aio
    In:  EPIC3Le Cannet, Editions Aio
    Publication Date: 2020-07-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 30
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    Dating Laboratory, University of Helsinki
    In:  EPIC3Helsinki, Finland, Dating Laboratory, University of Helsinki
    Publication Date: 2019-09-03
    Repository Name: EPIC Alfred Wegener Institut
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  • 31
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    University of Hawaii
    In:  EPIC3Honolulu, Hawaii, U.S.A., University of Hawaii
    Publication Date: 2016-09-27
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 32
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2016-10-29
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 33
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    OXFORD UNIV PRESS
    In:  EPIC3Journal of Plankton Research, OXFORD UNIV PRESS, 8(3), pp. 549-555, ISSN: 0142-7873
    Publication Date: 2017-02-02
    Repository Name: EPIC Alfred Wegener Institut
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  • 34
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
    Type: Miscellaneous , notRev
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  • 35
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 36
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 37
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
    Type: Thesis , notRev
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  • 38
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    In:  EPIC3Environmental seminar, BSH, Hamburg
    Publication Date: 2017-02-13
    Repository Name: EPIC Alfred Wegener Institut
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  • 39
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    In:  EPIC3. “Day of Biology“-Meeting, Technical University, Aachen, Germany
    Publication Date: 2017-02-13
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  • 40
    Publication Date: 2017-02-13
    Repository Name: EPIC Alfred Wegener Institut
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  • 41
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    Marine Geology, Elsevier
    In:  EPIC3Amsterdam, Marine Geology, Elsevier
    Publication Date: 2016-10-04
    Repository Name: EPIC Alfred Wegener Institut
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  • 42
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    Universität Hamburg
    In:  EPIC3Berichte des Zentrums für Meeres- und Klimaforschung der Universität Hamburg, Universität Hamburg
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 43
    Publication Date: 2017-02-02
    Repository Name: EPIC Alfred Wegener Institut
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  • 44
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    Journal of Geochemical Exploration, Elsevier
    In:  EPIC3Amsterdam, Journal of Geochemical Exploration, Elsevier
    Publication Date: 2016-10-07
    Repository Name: EPIC Alfred Wegener Institut
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  • 45
    Publication Date: 2016-10-06
    Description: https://www.researchgate.net/publication/230891291_The_Orbital_Theory_of_Pleistocene_Climate_Support_frim_a_Revised_Chronology_of_the_Marine_d18O_Record
    Repository Name: EPIC Alfred Wegener Institut
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  • 46
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    Alfred-Wegener-Institut für Polar- und Meeresforschung
    In:  EPIC3Bremerhaven, Alfred-Wegener-Institut für Polar- und Meeresforschung
    Publication Date: 2016-10-21
    Repository Name: EPIC Alfred Wegener Institut
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  • 47
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
    Type: Miscellaneous , notRev
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  • 48
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 49
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    Abt. f. Syst. Geobot.; RWTH-Aachen
    In:  EPIC3Abt. f. Syst. Geobot.; RWTH-Aachen, 182 p.
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 50
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    Universität Hamburg
    In:  EPIC3Berichte des Zentrums für Meeres- und Klimaforschung der Universität Hamburg, Universität Hamburg
    Publication Date: 2017-02-09
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  • 51
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    Alfred Wegener Institute for Polar and Marine Research
    In:  EPIC3Alfred-Wegener-Institute for Polar- and Marine Research, Bremerhaven, Bremerhaven, Alfred Wegener Institute for Polar and Marine Research
    Publication Date: 2015-12-02
    Repository Name: EPIC Alfred Wegener Institut
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  • 52
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    Geological Society of America Bulletin
    In:  EPIC3Boulder, Geological Society of America Bulletin
    Publication Date: 2015-12-14
    Repository Name: EPIC Alfred Wegener Institut
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  • 53
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    Earth and Planetary Science Letters
    In:  EPIC3UK, Earth and Planetary Science Letters
    Publication Date: 2015-12-16
    Repository Name: EPIC Alfred Wegener Institut
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  • 54
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    Marine Geology
    In:  EPIC3Amsterdam, Marine Geology
    Publication Date: 2016-02-04
    Repository Name: EPIC Alfred Wegener Institut
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  • 55
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2016-06-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 56
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2016-06-27
    Repository Name: EPIC Alfred Wegener Institut
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  • 57
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    Honeywell ELAC Nautik GmbH
    In:  EPIC3Kiel, Honeywell ELAC Nautik GmbH
    Publication Date: 2014-10-25
    Repository Name: EPIC Alfred Wegener Institut
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  • 58
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    Proceedings of NATO/NSF A.R.W. Symposium
    In:  EPIC3Grenoble, Proceedings of NATO/NSF A.R.W. Symposium
    Publication Date: 2015-09-15
    Repository Name: EPIC Alfred Wegener Institut
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  • 59
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    ATM Corporation
    In:  EPIC3Milwaukee, WI, USA, ATM Corporation
    Publication Date: 2017-10-27
    Repository Name: EPIC Alfred Wegener Institut
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  • 60
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    micromeritics
    In:  EPIC3Norcross, GA, micromeritics
    Publication Date: 2017-10-27
    Repository Name: EPIC Alfred Wegener Institut
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  • 61
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    Kosmos-Bibliothek
    In:  EPIC3Stuttgart, Kosmos-Bibliothek
    Publication Date: 2017-11-03
    Repository Name: EPIC Alfred Wegener Institut
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  • 62
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    Nieders. Geol. Verein
    In:  EPIC3Hannover, Nieders. Geol. Verein
    Publication Date: 2017-11-25
    Repository Name: EPIC Alfred Wegener Institut
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  • 63
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    Notgemeinschaft der deutschen Wissenschaft
    In:  EPIC3Berlin, Notgemeinschaft der deutschen Wissenschaft
    Publication Date: 2017-11-25
    Repository Name: EPIC Alfred Wegener Institut
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  • 64
    Publication Date: 2018-04-03
    Repository Name: EPIC Alfred Wegener Institut
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  • 65
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    "Meteor" Forsch.-Ergebnisse
    In:  EPIC3Berlin-Stuttgart, "Meteor" Forsch.-Ergebnisse
    Publication Date: 2018-04-12
    Repository Name: EPIC Alfred Wegener Institut
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  • 66
    Publication Date: 2018-08-28
    Description: Summary Holocene sediments of the North Lagoon, Bermuda, were studied with shallow seismic reflection profiles (200 km CSP-survey, UNIBOOM-system) and vibration coring (40 sediment cores, pneumatic vibration corer, Meischner et al., 1981). Seismic Stratigraphy Four seismic sequences are distinguishable by seismic stratigraphy. All seismic sequences correspond to depositional sequences built up during high sea levels in interglacial times. The seismic sequences are separated by unconformities which are often strongly reflective and correspond to emersion planes during glacial phases. The upper sequence (sequence 4) is related to Holocene sediments. The pre-Holocene bedrock is divided into three different seismic sequences (Kuhn et al., 1981): Sequence 1: oldest Pleistocene sequence (pre-Sangamon sea-level highstands), upper boundary with levelled relief (lower boundary not discernible), composed of strongly cemented carbonate sediments, forms the bedrock below Three Hill Shoals Sequence 2: Sangamon (125 ky sea-level highstand), distinct surface morphology, forms the bedrock of a large area below Holocene sediments, Holocene reefs grew up on elevations of the sequence 2 surface, the Holocene reef rim was developed on an elevated rim of sequence 2 Sequence 3: youngest Pleistocene sequence (Sangamon, 105 and 85 ky sealevel highstands lower than recent), deposited mainly in depressions of the bedrock deeper than -15 m below recent Mean Sea Level, levelling the older relief, peat sedimentation in places The distribution of recent reef areas and lagoonal basins is strongly controlled by pre-Holocene topography and geology of the bedrock. During the Holocene approx. 1050 x 106 m3 of carbonate sediments were deposited in the North Lagoon (290 km2) and approx. 1350 x 106 m3 in the reef rim area (170 km2). Sedimentology There are no larger oscillations of the Holocene sea level identifiable in the sedimentological record. The pre-Holocene topography was gradually drowned during the Holocene sea-level rise. At first, the depositional depressions were separated and landlocked. Fresh water peat marshes, fresh water ponds, marine ponds and bays were formed. With rising sea level, the land barriers were more and more eroded, drowned and lost their influence on the back-barrier sedimentation area. Autochthonous and allochthonous peat, lime gyttja and carbonate mud are a typical transgressive back-barrier sediment sequence. After destruction of the barrier, the depositional milieu changed from restricted marine to normal marine, open lagoonal. Sea-grass sediments and nearly mud-free carbonate sand were deposited in shallow water in an exposed environment. Hydrodynamic energy decreases with increasing water depth in the lagoonal basin. A more densely growing reef rim and intralagoonal reef growth added to the protection of the deeper lagoonal floors. Fine-grained sediments were deposited in this environment. They are distributed over a large area of the North Lagoon and form the top of the transgressive lagoonal sediment sequence. Holocene reefs mainly developed on rises of the pre-Holocene surface. In the early Holocene, solid reef build-ups were able to keep up with the rapid rise of sea level. Sand pockets in the reefs were left behind and filled up mainly in the later Holocene. The percentage of fine-grained sediments, produced and resuspended in the reef rim and deposited in the near lagoonal back-reef zone, increased during the Holocene. Two models of Holocene sedimentation in a depression and on an elevation of the pre-Holocene surface illustrate the dependence of vertical facies gradation on pre-Holocene topography. Trends of the mostly polymodal grain-size distributions of the Holocene sediments are a coarsening-upward in the back-barrier and a fining-upward in the lagoonal sediment sequences. Change in the composition of the molluscan fauna in the Holocene sediments (particle size 〉 2000 µm) is an Indication for fades changes. Gastropods are abundant in the basal backbarrier sediments. Bivalves are rare and their diversity 1s low. Sea-grass sediments contain Codakia orbicularis and Astraea phoebia shells. In the sheltered lagoonal environment shell fragments 〉 2000 µm become rare, common species are Gouldia cerina, Pitar fulminata and Finella sp. (approx. 1000 µm). Fine-grained reef-rim derived sediments differ from lagoonal sediments by a higher percentage of Homotrema rubrum fragments and Alcyonaria spicules.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Thesis , notRev
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  • 67
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    aerodata Flugmeßtechnik GmbH
    In:  EPIC3Braunschweig, aerodata Flugmeßtechnik GmbH
    Publication Date: 2016-07-20
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 68
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
    Type: Miscellaneous , notRev
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  • 69
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    Abt. f. Syst. Geobot.; RWTH-Aachen
    In:  EPIC3Abt. f. Syst. Geobot.; RWTH-Aachen, 154 p.
    Publication Date: 2017-02-09
    Repository Name: EPIC Alfred Wegener Institut
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  • 70
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    PANGAEA
    In:  EPIC3Bremerhaven, PANGAEA
    Publication Date: 2017-06-01
    Repository Name: EPIC Alfred Wegener Institut
    Type: PANGAEA Documentation , notRev
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  • 71
    Publication Date: 2018-09-21
    Description: Some fifty years after the Snellius I expedition (1929-1930) a Dutch-Indonesian joint expedition is carried out (1984-1985) in the Eastern Indonesian archpelago. Based on two months (September -October 1984) of research at nine different reef localities, a first report will be presented on the general morphology, composition and condition of recent and fossil reefs of these areas. The research areas that will be discussed are the following: Ambon: In the bay of Ambon fringing and patch reefs heavily damaged by silting up, caused by soi1. erosion on the island. North East Ambon an elevated reef from the old Pleistocene. Lucipara islands: Exposed very isolated atoll with some sand cays. Tukang Besi islands: Atoll reefs of Kaledupa. Binongko reef terraces; fossil cliffs modelled from massive Pleistocene reef limestone by coastal abrasion during tectonic uplift of the island; extensive reef terrace dating from the last interglacial; living reef not at the moment constructive. Sumba: East Sumba fringing reefs with influence of land and population. Young Pleistocene reef near Melolo, older terraces higher up. Komodo: Various fringing and patch reefs bordering the east side of the National Park of Komodo. Current swept reefs in the strait of Linta. Gililawa Laut and Tinandja lo~r Miocene reefs. Sumbawa: Fringing reefs in Telok Moti Toi and Sanggar bay near Tambora volcano (erupted in 1815). Coral growth in Bima bay. Pleistocene reef north east of Bima. Taka Bone Rate: Large pseudo atoll with small sand cay reefs (e.g. Tinandja) exposed reefs, coral banks and lagoons. Salayer: fringing reefs at west coast around islands Guang and Sahuluan. Pliocene reefs on both islands; Bahuluan with volcanic core. Sulawesi: Coral reef complex on the shallow shelf off South West Sulawesi, with three rows of reefs, most emerging as sand cay reefs. Because of young Holocene reg~ession in front of Ujung Pandang. Influence of sedimentation and population. Apart from these investigations during the Snellius II expedition, a long term project has been carried out since 1979 in the last area mentioned. A continuation of reef research is planned there, in close cooperation with UnHas (University of Ujung Pandang). The presentation of results will be accompanied by maps and photographs.
    Keywords: Reef geology ; Geomorphology ; ICRS5
    Repository Name: National Museum of Natural History, Netherlands
    Type: Article in monograph or in proceedings
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  • 72
    Publication Date: 2018-08-14
    Keywords: oceanography ; zoogeography ; taxonomy ; collecting stations ; faunistic assemblages ; list ; Canary Islands ; Archipelago of Cape Verde ; Archipelago of Madeira ; Archipelago of the Azores ; North Africa ; North Atlantic Ocean ; CANCAP-Project
    Repository Name: National Museum of Natural History, Netherlands
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  • 73
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.3 (1988) nr.1 p.297
    Publication Date: 2015-05-08
    Description: In this precursory paper to the forthcoming Flora Neotropica monograph of Rollinia 12 new species are described. One new combination is made, and there is a note on the correct author citation for Rollinia dolabripetala. Mr. E. J. van Marle, a former student at the University of Utrecht, contributed the description of one of the new species.
    Repository Name: National Museum of Natural History, Netherlands
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  • 74
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.3 (1988) nr.1 p.345
    Publication Date: 2015-05-08
    Description: There exist three different kinds of leaf arrangement in neotropical species of Rinorea. 1. an alternate leaf arrangement consisting of only laminar leaves; 2. an alternate leaf arrangement consisting of laminar leaves in the apical part of the branchlets and scale-like ones subpersistent in the basal part; 3. an apparently opposite leaf arrangement consisting of laminar leaves together with a pair of inconspicuous and soon deciduous scale-like leaves at the base of the inflorescences. In this article hypotheses have been constructed how one kind of leaf arrangement can be derived from the other, how these three different kinds of leaf arrangements can be correlated with the arrangements of the inflorescences and those of the branchlets, and finally how an apparently opposite leaf arrangement also can be correlated with a so called Fagerlind tree model.
    Repository Name: National Museum of Natural History, Netherlands
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  • 75
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.1 (1983) nr.1 p.49
    Publication Date: 2015-05-08
    Description: Twelve species of terricolous microlichens from the Angmagssalik District, Southeast Greenland, are reported: Caloplaca friesii, C. livida, Lecanora boligera, Lecidea oligotropha and Leciophysma arctophila, which are new to the lichen flora of Greenland, Rinodina conradi, which is new to the eastcoast, and Baeomyces roseus, B. rufus, Buellia geophila, B. punctata, Caloplaca tornoensis and Mycoblastus tornoensis, new to Southeast Greenland. In a discussion of the greenlandic distribution, unpublished records from the herbarium of Copenhagen (C) are incorporated. Notes on the habitats are given and the pertinent phytosociological units indicated. Some morphological and anatomical characters are commented upon briefly.
    Repository Name: National Museum of Natural History, Netherlands
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  • 76
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.347 (1970) nr.1 p.271
    Publication Date: 2015-05-08
    Description: The three species Galium silvaticum L., Galium aristatum L. and Galium schultesii Vest show differences in morphology, cytology and geographical distribution. These differences are described and discussed. Crossing experiments between the three species were without results. No hybrid could be obtained. Galium silvaticum, Galium aristatum and Galium schultesii must be considered as separate species.
    Repository Name: National Museum of Natural History, Netherlands
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  • 77
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    In:  Zoölogische Monographieën (0169-8478) vol.1 (1973) nr.1 p.3
    Publication Date: 2015-05-08
    Description: Although a large number of Tortricoid species and several genera from the Indo-Malayan region have been described by earlier authors (Walker, Snellen, Walsingham, Meyrick, and a few others), no survey of the present group has ever been made. Edward Meyrick, the author of most of the new names, has never attempted a synopsis of the Olethreutinae. He made surveys of the Australian and New Zealand Tortricoidea (1911), but the results are too superficial for our modern standards. During a long sojourn, working and collecting in Java, I became greatly fascinated by that fauna. Having completed a number of preliminary studies of the subfamily Tortricinae (1939 et seq.), I turned next to the South Asiatic, especially Javanese, Olethreutinae. After a long delay due to World War II, their revision has been initiated by the study of the two then least known and most confused genera, Bactra Stephens and Lobesia Guenée (Diakonoff, 1950 et seq.).
    Repository Name: National Museum of Natural History, Netherlands
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  • 78
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.1 (1983) nr.1 p.381
    Publication Date: 2015-05-08
    Description: The 16 recognized species of Sorocea are listed with their synonyms and distribution. Two new taxa are described: S. steinbachii C.C. Berg and S. hirtella Mildbread ssp. oligotricha Akkermans & Berg. Three new combinations are made: S. muriculata Miquel ssp. uaupensis (Baillon) C.C. Berg, S. trophoides W. Burger ssp. rhodorachis (Cuatrecasas) C.C. Berg, and S. sprucei (Baillon) Macbride ssp. saxicola (Hassler) C.C. Berg. A key to the species is presented.
    Repository Name: National Museum of Natural History, Netherlands
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  • 79
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.2 (1985) nr.1 p.305
    Publication Date: 2015-05-08
    Description: -The problems of reconstructing historical relationships for areas of endemism from distributional data for groups of taxa and the cladistic relationships among the members of those groups can be solved by applying the two principles of parsimony and mutual inclusion or exclusion (compatibility) of components. Components can be extracted from a data matrix by means of transcription into partial monothetic sets. The data matrix thus derived represents the distribution over areas for the monophyletic groups in one or more cladograms. It is derived from two different matrices by boolean multiplication. The first matrix gives the binary representation of distributions of taxa over areas of endemism; the second describes the cladogram for the same taxa, in terms of character states converted into binary form by additive binary coding. The derived data matrix can be used in historical biogeography to represent the given phyletic data ( Assumption 0 here newly defined), and can be amended to reflect Assumptions 1 or 2 to accomodate the problems of wide-spread taxa and missing areas. Areacladograms are determined from the derived matrix by searching for the largest sets of mutually compatible components. Area-cladograms are evaluated in terms of support (vicariance) and contradiction (ad hoc interpretations such as dispersal and extinction). Area-cladograms that best fit the data matrix regarding the balance between support and contradiction are selected as the best possible recontructions of relationships among the areas of endemism. The procedure is illustrated by the example of the poeciliid fish genera Heterandria and Xiphophorus, and several other standard examples.
    Repository Name: National Museum of Natural History, Netherlands
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  • 80
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.2 (1985) nr.1 p.505
    Publication Date: 2015-05-08
    Description: Aublet based Tontelea and its only named species, T. scandens, on material he collected in French Guiana, illustrated as pl. 10 in the original publication. Aublet’s specimens are incorporated in the herbarium of J. J. Rousseau (now located in the Paris Herbarium in herbier Denaiffe) and also in the Herbarium of the British Museum. The sheet in herbier Denaiffe was identified by Lanjouw and Uittien (1940) as the original for Aublet’s pl. 10, which shows a flowering twig, analysis of a flower, and a detached leaf much larger than the leaves on the twig. From a photograph of this sheet it appears that the inflorescence is reproduced only in fragmentary form in the drawing. In the latter the inflorescence is represented as a rather short, few-branched, flowering twig, whereas in the specimen the inflorescence is strictly dichotomously branched many times with occasional supernumerary branches in the leaf axils. The sheet also has four detached leaves.
    Repository Name: National Museum of Natural History, Netherlands
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  • 81
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.2 (1985) nr.1 p.197
    Publication Date: 2015-05-08
    Description: This catalogue provides an annotated listing of the liverworts and hornworts from the Guianas (Guyana, Surinam, French Guiana), based on the literature and on new data that have become available in the framework of the “Flora of the Guianas” project. In total 375 species in 93 genera are recorded, including more than 100 species and 28 genera new to the Guianas. A list of synonyms (including 30 new ones), a systematic arrangement of the genera and families, and an index to the collectors are also given.
    Repository Name: National Museum of Natural History, Netherlands
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  • 82
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.3 (1988) nr.1 p.243
    Publication Date: 2015-05-08
    Description: This paper follows upon an earlier paper in the series “Studies in Annonaceae” (Maas et al. 1986). Twelve new species are described, viz. 2 in Duguetia, 1 in Ephedranthus, 5 in Guatteria, 2 in Hornschuchia, 1 in Tetrameranthus, and 1 in Unonopsis. A new combination is made in Enicosanthellum. Some amendments and additions to the revision of Tetrameranthus (Westra 1985), including an updated key, are given. Monocarpia euneura Miq. appears to have priority over M. marginalis (R. Scheffer) James Sincl. Additional collections have been made of the rare species Bocagea longepedunculata Martius, Xylopia crinita R.E. Fries, and Xylopia excellens R.E. Fries. Attention is drawn to several recent collections from Bahia, Brazil, which are perhaps referable to Unonopsis stipitata Diels. H. León, Popayán, and D. Sánchez S., Medellín, contributed to three of the new species.
    Repository Name: National Museum of Natural History, Netherlands
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  • 83
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.350 (1971) nr.1 p.269
    Publication Date: 2015-05-08
    Description: Some rain and savanna forests of western Suriname (Corantijn R., Winana Creek; Upper Marataka R.; Upper Nickerie R;) were studied and their composition was compared with that of forests of other parts of Suriname and Guyana. The savanna forests of western Suriname proved to be much related to Guyanan ( Walabaand Dakama-) savanna forests as described by Davis & Richards (1934) and Fanshawe (1952). On the other hand, there was less relationship as regards rain forests of western Suriname when compared with ones of Guyana and other parts of Suriname, except for the Demerara greenheart forest of the Upper Marataka R., which was closely related to the Demerara greenheart forests of Guyana as described by Davis & Richards (1934). In addition an upland rain forest was studied near Blanche Marie falls, Upper Nickerie R., which proved to be very much like that of the Stofbroekoe Mts., eastern Suriname, as described by Schils (1960). Species/area curves for some rain and savanna forests are given. The geographical distribution of some common western Surinam tree species was studied; of the seventeen species studied one was endemic for Suriname. An annotated list of all species of trees and palms occurring in the explored areas is provided.
    Repository Name: National Museum of Natural History, Netherlands
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  • 84
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.375 (1972) nr.1 p.213
    Publication Date: 2015-05-08
    Description: Three sections with a total number of four species of the genus Phyllanthus have been examined. The pollen grains show a strong resemblance to each other and also the taxonomic arguments to differentiate between the three sections proved to be rather weak. Because of both palynological and taxonomic reasons the sections Ceramanthus Baillon, Cluytiopsis Mueller Arg. and Anisolobium Mueller Arg. have been united into one section; viz. section Ceramanthus Baillon s.l.
    Repository Name: National Museum of Natural History, Netherlands
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  • 85
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.509 (1981) nr.1 p.23
    Publication Date: 2015-05-08
    Description: Neohattoria Kamim. is a monotypic genus of the Jubulaceae (= Frullaniaceae) with a single species, N. herzogii (Hatt.) Kamim., known from central to northern Japan and the southern part of the Kurile Islands. The present genus was segregated from Frullania by Kamimura (1961; sub. nom. Hattoria Kamim. nom. illeg., non Schust., 1961) on the basis of the branching type, the shape of the first leaf and underleaf on branch, the total lack of secondary pigmentation, the uniform cell structure of the stem in cross section, and the strongly toothed leaf lobes. The generic concept of Neohattoria was greatly expanded by Schuster (1970), who included eight species and classified them into two subgenera, subgen. Neohattoria (with a single species) and subgen. Microfrullania Schust. (with seven species); however, Hattori et al. (1972) transferred all species of subgen. Microfrullania to a newly segregated genus Schusterella Hatt. et al., thus retaining the monotypic status of Neohattoria. As already described and illustrated by Hattori (1955), Kamimura (1961), Mizutani (1961), Ladyzhenskaja (1963), Schuster (1970), and Hattori et al. (1972), Neohattoria herzogii is closely related to species of both Jubula and Frullania. Regarding the taxonomic desposition of Neohattoria, Mizutani (1961) and Mizutani & Hattori (1969) placed it with Jubula in a subfamily Jubuloideae of Lejeuneaceae and Hattori et al. placed it in Jubulaceae (s. lat.). But, Kamimura (1961), Schuster (1970, 1979), and Guercke (1978) placed it more close to Frullania, e.g. in a subfamily Frullanioideae of Jubulaceae (s. lat.); more recently, Asakawa et al. (1979b), admitting three distinct families, Jubulaceae, Frullaniaceae, and Lejeuneaceae, placed Neohattoria and Jubula in the Jubulaceae (s. str.) but Frullania and Schusterella in the Frullaniaceae.
    Repository Name: National Museum of Natural History, Netherlands
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  • 86
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.94 (1946) nr.1 p.5
    Publication Date: 2015-05-08
    Description: As an introduction to a number of researches of his own the author wishes to give the following data: „Veen” has two meanings in Dutch: 1. in a petrographic sense (peat) Von Büllow’s definition was accepted: „Torf” ist zu deflnieren als ein meist dunkles, kohlenstoffreiches und ± saures Gemenge unvollständig spezifisch-zersetzter Pflanzenteile, das erdgeschichtlich jüngste Glied der Verwantschaftsreihe der Kohlen, dessen Bildung noch heute andauert.” 2. in a plant-sociological-geographic sense (bog) the following definition has been suggested: a bog is a plot, the surface of which consists of a layer of peat, either covered or not with vegetation, with which that layer is genetically connected. The classification of bogs according to their position with regard to the water-level of the surroundings (Staring) and that of the geological chart were rejected on account of their ambiguous character. The classification suggested by Van Baren according to the environment in which the bogs have been formed, was likewise thought insufficient. Preference was given to the classification according to the plants which gave rise to the peat (eutrophic, mesotrophic and oligotrophic bogs) and according to the origin of the water needed for peat formation (topogenous, ombrogenous and soligenous bogs). The conditions of peat-formation are of a botanical (presence of a vegetation and micro-organisms), climatologic (presence of a certain temperature and moisture) and geological nature (presence of a basin, valley or dead river-branch, certain level of ground water, a possible impervious layer). With reference to a number of authors (Picardt; Van Lier; Grisebach, Venema and Staring; Weber) the alteration in conception as to peatformation from the 17th via the 18th and 19th to the 20th century has been given. The word „Peel” cannot be derived from „palus”. Nothing is certain about its origin. It may mean the low land, bog or marsh. The bogs of the Peel lie on the Brabant-Limburg border-plateau (fig. 2). Lorié and Pannekoek van Rheden have shown that the peatformation of the Peel is likely to have occurred in channels, which have been formed by the Meuse, in co-operation with wind and rain (fig. 4). The bogs were therefore in the first instance topogenous formations, which afterwards developed into ombrogenous bogs. For his own research the author collected peat in three ways: 1. by cutting lumps of peat from open profiles; 2. by boring with a simple peat-bore (photograph 1); 3. by boring with the Utrecht peat-bore, an improvement on Dachnowski’s (fig. 5). To assist in the pollen-analytic examination the samples were treated according to Erdtman’s method. The latter has the following advantages compared with the usual treatment with a 10% KOH-solution: 1. the surface-structures of the pollen-grains are more distinct and as a result the grains themselves can be recognized better; 2. the pollen is more concentrated, so that in spite of the method taking up much time, a saving of time is possible. How the method is applied may be found in the chapter concerned (p. 38 and following). For the stratigraphic examination the samples were broken apart in a glass-bowl of water and viewed with a binocular microscope. Dry sandy samples were broken in water, when seeds and other vegetative parts came floating to the top; next they were put with a brush on thick blotting paper and studied through the binocular microscope. The designations for the sediments and species of peat have been derived from Fægri & Gams. For Scheuchzeria peat a new designation has been added. A plea was made for replacing the word pollen-analysis by „palynology”. A survey of the observations and examinations up to abt. 1935 closes the introduction (see the diagrams of Weber, Erdtman and Duyfjes in the figs. 6, 7, 8 and 9). The author’s own research refers to the Southern and Astense Peel, as in the remaining grounds of the geological chart indicated I 4v (= raised bog) no samples could be taken owing to the digging off having progressed too far. 10 profiles were examined. The situation of the bore-sites has been given in the geological chart of the grounds (fig. 3). The result of the examination (figs. 10—27) and the discussion on it may be summerized as follows: Zoning of pollen-diagrams The sub-zoning of the late- and post-glacial periods according to Blytt & Sernander has proved useful as a zoning of pollen-diagrams, provided atlantic and sub-boreal are joined. It is desirable to replace Blytt & Sernander’s terminology by a different one, because the authors gave a climatologic connotation to their names of periods. The limit between pleistocene and holocene was drawn between preboreal and boreal as Florschütz did. As phases of the holocene the following names were suggested: young post-glacial = sub-atlantic mid post-glacial = sub-boreal and atlantic old post-glacial = boreal. Neither in the Peel nor elsewhere in Holland have Allerød-deposits been found. They are not likely to be found either, as on account of the long distance from the land-ice-margin the flora will have been hardly or not at all influenced by the Allerød interstadial period. For Holland therefore the zoning of the late-glacial according to Firbas (1935) may be considered sufficient. The names of the periods do not bear a climatologic connotation as those of the post-glacial phases do. For the sake of a unity the following names have been suggested: young late-glacial = pre-boreal mid late-glacial = sub-arctic period old late-glacial = arctic period. Forest-history In a table (p. 98), in which likewise the Peel diagrams of Weber, Erdtman and Duyfjes have been inserted, the examined profiles have been arranged from North to South. From each profile it has been stated whether it originated in a certain period (+) or not (—). The sub-arctic phase was characterized by forests of Betula and Pinus and was followed by the pre-boreal phase, in which Corylus and Alnus occurred. Also from the other Dutch diagrams (see list on p. 99) it appeared that in the Netherlands the Alnus pollen occurs with an equal frequency before, during and after that of the Quercetum mixtum. The old post-glacial zone of the diagrams shows a peak in the Pinusline. In contrast with the from Mid-Europe there is not always a maximum in the Corylus-curve after the Pinus-peak. In other Dutch diagrams this phenomenon is likewise found. Only in 28% of all Dutch profiles with a boreal zone does a hazel-maximum succeed a Pinus one. They often co-incide (16%), while in the remaining cases no hazelpeak has been established. There is no fixed order of sequence in the occurrence of the components of the Quercetum mixtum, either in the Peel or elsewhere in Holland. The mid post-glacial is the phase of culmination of warmth-loving forest elements: Alnus pollen shows the highest percentage in this zone. Quercus pollen also occurs in great quantities, while Ulmus and Tilia take up an important place up to the „Grenzhorizont”. The absolute and empiric Fagus pollen limits are found at different heights in the mid post-glacial zone of the diagrams, the rational limit lies somewhere near the „Grenzhorizont”. In the young post-glacial phase the Fagus pollen attains fairly high percentages (up to 30%). The maxima in the East and South-east of the Netherlands are between 20% and 38%; they decrease towards the coast and increase towards the South-east (Hautes Fagnes, Belgium) and East (Germany). It seems incorrect to class the Netherlands almost entirely among the oak-alderterritory poor in beeches, as Firbas did. An attempt has been made to fit the Peel-diagrams into Overbeck & Schneider’s zonation system. For the territory for which it has been made there are already difficulties (p. 104), for use in the Peel and other Dutch diagrams there are even more objections (p. 68, 104). Godwin’s zonation system appeared to be a little less forced, but not quite useful on account of too many details. From his horizons that of Ulmus proved useless for the continent. Neither for the Peel nor for the Netherlands and its surrounding territory can a detailed zonation system be designed. It has proved difficult to proceed any farther than Rudolph’s „Grundsukzession”: birch, pine-hazel-mixed oak-forest-beech, in which the alder generally joins the mixed oak-forest and the hornbeam the beech. Before drawing far-reaching conclusions from the course of the curves (as has been done by some authors) more palynological researches are needed in accordance with the actuality principle, known from geology. Pollen-grains from warmth-loving trees in seemingly sub-arctic spectra In profile 4 (Deurnse Peel II) pollen-grains of Abies, Alnus, Picea, Tilia, Ulmus and Corylus were found in the „late-glacial” zone (figs. 14, 15). Investigations were made as to which of the following possibilities would be the cause of their appearance: 1. in taking and preparing the samples pollution occurred; 2. pollen-transport over long distances has taken place; 3. the pollen-grains found have got secondarily into the deposit; 4. warmth-loving trees have occurred in favourable circumstances in the late-glacial phase or 5. in an interstadial period or in an interglacial phase. The said pollen-grains probably hail from a Würm interstadial or interglacial phase. Interglacial peat On the site of the bore-point 7 it was possible to collect samples from the layers under the peat. The upper 40 cm of the diagram Griendtsveen IX (fig. 27) of this profile proved a repetition of the lower 40 cm of the Griendtsveen I profile (fig. 18). The diagram shows that pollen of Carpinus, Picea and Abies occurs showing the deposit to be of interglacial age. The pollen-curves, however, pass unnoticed from an interglacial into a post-glacial portion. The limit is likely to be found between the two, about 30 cm below the mowing field. There is therefore a great stratigraphic hiatus. Pollen-analytically it could not be decided from which interglacial period the profile hails; on account of its situation on the middle terrace, it was deemed likely that it was an Eem sea deposit. The examined profile probably corresponds to Jessen & Milthers’ zone g; showing it to have been formed at the end of the Eem sea period. The Meuse therefore cannot have flowed through this part of the Astense Peel after the mid Eemean phase. Stratigraphy This is difficult to summarize. Compare various profiles. Individual mention may be made here of: 1. peat on a podsol layer; this was found in two places (Deurnse Peel I Kraaienhut and Griendtsveen VIII). Peat-formation may be thought to have occurred in the following way: heather started growing on drift-sand giving rise to a podsol layer. As the latter is impervious the vegetation surface became marshy. The heath was replaced by a Caricetum from which peat arose. Gradually more Eriophorum occurred, from which almost pure vaginatum peat arose. The bog-surface grew moister and moister, Sphagnum cuspidatum and Scheuchzeria could grow on it and formed a „Vorlaufstorf”. Only then could non-extremehydrophile Sphagna join in peat-formation. 2. the occurrence of Scheuchzeria-peat after the „Grenzhorizont” period. This species of peat, which is often found at the basis of the old Sphagnum-peat as a mesotrophic transition vegetation, has for the Netherlands only been found in the young post-glacial phase in the Peel (Deurnse Peel I Kraaienhut, Griendtsveen V and VIII and Nederweerd). At present the plant is very rare. The severe decline of this plant was also observed elsewhere. Probably it is caused by the gradual drying up or reclaiming of the raised bogs. Of the present station of Scheuchzeria near Ommen a short description has been given (p. 59 and photographs 2, 3, 4). 3. the „Grenzhorizont”. Where the young Sphagnum-peat has not been dug for the preparation of moss-litter, the Peel bogs show a clear „Grenzhorizont” (photograph 8). The conceptions about its origin have been discussed. The distinct separation between the old and the young Sphagnum-peat was not considered sufficiently explained. Though on the whole the „Grenzhorizont” is synchronous in the North-west European profiles, the point of transition from old to young Sphagnumpeat was fairly unstable and easily changeable as to time. Generally the date of the „Grenzhorizont” is fixed at about 500 A.D., though there are differences in opinion. There is a lack of archeological correlation which renders a correct dating impossible. Interference of man in the Peel Three ways of interference were stated: 1. peat has been dug off for the greater part in the territory of the Peel: young Sphagnum-peat for the preparation of moss-litter, old Sphagnum-peat for fuel. The trees which appeared when the bog was dug up in the „Veenderij der Maatschappij Griendtsveen” are sometimes in so good a condition, that they are used for building sheds. The 1 st, 2nd and 4th beam in the foreground of the shed in photo 5 has been sawn from a 30 m long subfossil pine. 2. in a native peat-digging it was possible to collect recent young Sphagnum-peat. 40 to 50 years ago the peasants living there had dug peat in holes, which were afterwards left to themselves. Sphagnum started growing again and the holes were filled in again. The diagram (fig. Griendtsveen VII) represents the surrounding heath with scattered pines and birches, sown by the wind, and a pine-plantation close by. 3. in the profiles Nieuwe Peel, Griendtsveen VI and VII it has been fixed by the indications given by Firbas, that only in the surface layers of the bog has corn-pollen occurred. So in these parts cultivation of cereals will be of recent date. This also appeared from the history of the reclamation of the said territory.
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  • 87
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.412 (1974) nr.1 p.235
    Publication Date: 2015-05-08
    Description: Dicranella riparia (H. Lindb.) Mårt. & Nyh. is reported for the first time from Greenland, where it was found on a fluvioglacial delta in the Angmagssalik District in plant communities belonging to the association Calamagrosto-Ditrichetum (all. Calamagrostion neglectae). This is the sixth locality known, and the first outside Fennoscandia.
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  • 88
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.503 (1980) nr.1 p.7
    Publication Date: 2015-05-08
    Description: El género Plagiochila (hepatica) esta representada en las Islas Galapagos por ocho (8) especies diferentes: P. bursata (Desv.) Lindenbg., P. galapagona Inoue, P gradsteinii Inoue, P. guilleminiana Mont., P. inouei Grolle, P. scabrifolia Inoue, P. spinifera Ångstr. y P. subplana Lindenbg. El endemismo en este género es más alto que en otros géneros de las hepaticas, con cinco (5) especies que comienzan a conocerse solamente de los Galapagos ( P. galapagona, gradsteinii, scabrifolia, inouei, y spinifera). Las otras tres (3) son comunes y ampliamente distribuidas a lo largo de la America tropical. La mayoría de las especies estan restringidas a las zonas altas-húmedas de vegetación de las Islas Galapagos (matorrales de Zanthoxylum, Miconia y pampa) excepto P. guilleminiana muy común, la cual puede presentarse en la zona seca de transición de bosque. La más amplia variación de Plagiochila ha sido vista en Isabela (Cerro Azul), San Cristobal y Santa Cruz.
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  • 89
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.1 (1983) nr.1 p.43
    Publication Date: 2015-05-08
    Description: The species Polypodium banaense C.Chr. is transferred to Crypsinus. The recognition of a genus Phymatopteris Pic. Ser. (= Phymatopsis J.Sm.) separate from Crypsinus is discussed.
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  • 90
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    Unknown
    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.1 (1983) nr.1 p.33
    Publication Date: 2015-05-08
    Description: The six species of Curtia, including a hitherto undescribed species published here, as well as the monotypic genus Hockinia can be distinguished from each other by the seed coat structure. The anticlinal walls and the cuticle provide the most useful information. Curtia tenuifolia appears to be a complex species, but subsp. tenella can be readily separated from this complex by the seed coat structure. Heterostyly has been found in C. tenuifolia subsp. tenuifolia, C. obtusifolia, and Hockinia montana, but differences in seed coat structure can not be correlated with long-, short-, and equal-styled flowers. The differences in seed coat structure, the length of the seeds, and the number of cells per seed plead for maintaining Hockinia (closely related to Curtia) as a distinct genus. One new species of Curtia is described and a new combination is made.
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  • 91
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.1 (1983) nr.1 p.17
    Publication Date: 2015-05-08
    Description: SETTEN, A. K. van & KOEK-NOORMAN, J.: Studies in Annonaceae. VI. A leafanatomical survey of genera of Annonaceae in the Neotropics. — Bot. Jahrb. Syst. 108: 17—50. 1986. — ISSN 0006-8152. Within the scope of the multidisciplinary research project on systematics of Annonaceae, a survey of the leafanatomical features and their distribution in the neotropical Annonaceae is presented. The studied specimens form a rather homogeneous group, as may appear from the family description given here. A detailed study of the leafanatomical features reveals, that differences are mainly found in the indument, the position and contents of the idioblasts, the structure of the primary vein, the type of crystals in the epidermal cells, and the type of sclereids. Based on character states, phenetic similarities and differences are discussed and compared with the classifications of FRIES (1959) and WALKER (1971).
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  • 92
    facet.materialart.
    Unknown
    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.2 (1985) nr.1 p.327
    Publication Date: 2015-05-08
    Description: Haesselia roraimensis gen. et spec. nov. (Cephaloziaceae) from the foot of Mt. Roraima (Guyana) is described and figured. The new genus has been assigned to the subfamily Trabacelluloideae together with Fuscocephaloziopsis Fulf. and Trabacellula Fulf., two other neotropical genera of Cephaloziaceae with convex leaves.
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  • 93
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    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.1 (1983) nr.1 p.133
    Publication Date: 2015-05-08
    Description: One new species of Dorstenia from Brazil is described: D. carautae C.C. Berg, and four new combinations are made: D. cayapia Vellozo subsp. asaroides (Hooker) C.C. Berg, D. cayapia Vellozo subsp. paraguariensis (Hassler) C.C. Berg, D. cayapia Vellozo subsp. vitifolia (Gardner) C.C. Berg, and D. ramosa (Desvaux) Carauta, Valente & Sucre subsp. dolichocaula (Pilger) C.C. Berg. A list of and a key to the 22 Dorstenia species distinguished in south-eastern tropical America are presented, together with synonymy and distributional data.
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  • 94
    facet.materialart.
    Unknown
    In:  Miscellaneous publications of the University of Utrecht Herbarium (1572-6592) vol.2 (1985) nr.1 p.159
    Publication Date: 2015-05-08
    Description: Chemical analysis of representatives of about thirty genera of Lejeuneaceae has shown that the terpenoid and flavonoid content of the Lejeuneaceae is basically comparable to that of other Hepaticae and quite diversified. Among the terpenoids detected, some are common throughout the family (elemenenes, germacrenes), others are distributed more restrictedly and are indicative of evolutionary relationships among genera, e.g. borneols (Nipponolejeunea), pinguisanines (Acrolejeunea complex), striatenes (Ptychanthoideae, Omphalanthus complex), calamenanes ( Lopholejeunea) and labdanes (Ptychanthus, Tuzibeanthus). Flavonoids are present in smaller amounts than terpenoids and comprise some compounds unique to bryophytes (lutonarin, kaempferol-3-methylether). The genus Omphalanthus stands out by its total inability to biosynthesize flavonoids. At the species level the chemical constitution may vary considerably and in some species evidence for the existence of chemical races was detected.
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  • 95
    facet.materialart.
    Unknown
    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.363 (1971) nr.1 p.99
    Publication Date: 2015-05-08
    Description: The samples of the genus Calypogeia in the dutch institutional herbaria and private collections, those of C. arguta excluded, have been re-identified, according to the revision of the Swiss Calypogeias by Bischler (1957); distribution maps are given for all the taxa. More exact circumscriptions are given of several differentiating characters which were already established by previous authors. In C. fissa and C. sphagnicola the areolation of the leaves appeared to be a new differentiating character: in C. fissa the cells in the middle of the leaf show a great variation in length, whereas in C. sphagnicola the cell size is uniform. These differences are shown in histograms. C. muelleriana appeared to be restricted to the diluvial parts of the country, whereas C. fissa is common on both alluvium and diluvium; c. neesiana, C. sphagnicola and C. trichomanis are very rare, so that no clear geographical distribution can be given.
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  • 96
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.415 (1974) nr.1 p.1
    Publication Date: 2015-05-08
    Description: This study deals with the taxa of the section Rubus of the genus Rubus L., so far as they are found in the Guelders district within the flora of the Netherlands. It concerns fifty species and some subspecies and varieties, mainly of the subsections Fruticosi Wimm. et Grab. and Discolores P. J. Müller. The similarity with the bramble-flora of northern Germany is obvious. A number of species, that occur in the latter region are absent however. Species of Central-European hills and mountains are as good as limited to the southern border of the Veluwe, which is mostly considered to belong to the Subcentreuropean district. South-European, often calciphilous species are absent. The nomenclature in the genus Rubus is very confused. There is an abundance of homonyms and synonyms. The number of misidentifications is rather large, meaning that a great deal of the literature is unreliable. The descriptions with many authors are absolutely insufficient, and type-specimens are often with difficulty or not at all to be traced. The difficulties arise from the fact that many taxa are not clearly separated. Some of them are well distinguishable, others are related by transitions. From a geographical point of view there is much difference as well. Some species have as their area almost the whole of Europe, others are limited to a very restricted area. In addition there is a difference in chromosome numbers (from diploids (2n = 14) to hexaploids (2n = 42). Most taxa are tetraploid. The abundance of forms within the section Rubus arises from a partly apomictic, partly amphimictic propagation. To set up some order in all those differences, the author has made the following distinctions: morphologically there are the different ranks of species and infraspecific taxa. Geographically distinctions have been made by means of a code of the capitals A to D inclusive: A indicates the taxa with the largest area, D the local taxa. Cytologically a code of Roman numerals has been given: I for diploids, II for polyploids. Beside the introductory theoretical part a short description of all taxa of the section above the specific rank has been given. All species and infraspecific taxa of this section, that are found to occur in the Guelders district have been described in detail, with mention of the type-specimen. Pictures have been added of the newly described taxa, and of some others as well. Maps of the distribution in the Netherlands of all the taxa have been inserted.
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  • 97
    facet.materialart.
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    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.368 (1972) nr.1 p.95
    Publication Date: 2015-05-08
    Description: This paper is an addendum to the author’s (1971) paper. At the time that the latter paper was finished, there were difficulties in taking photographs of the newly described male fructifications. Subsequently those difficulties have been solved, and the present paper contains the photographs of the male fructifications of the type specimens of Hastystrobus muirii v. Kon., Masculostrobus harrisii v. Kon., and Pityanthus scalbiensis v. Kon., and the photographs of the male fructifications, as described in the above-mentioned paper, of Ginkgo huttoni (Heer) Sternberg and Brachyphyllum crucis Kendall. All specimens are preserved in the Division of Palaeobotany and Palynology, Botanical Museum and Herbarium, State University, Utrecht, The Netherlands. Most of the photographs were taken with the specimens illuminated obliquely in air, but some were taken with the specimens flooded with oil. This procedure is generally applied when the specimen requires enhancement of contrast, so that details are more evident than if the specimen was photographed dry.
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  • 98
    facet.materialart.
    Unknown
    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.516 (1983) nr.1 p.1
    Publication Date: 2015-05-08
    Description: Recently a multidisciplinary investigation program on the systematics of Annonaceae was started at Utrecht with special emphasis on the Neotropics. This project will be carried out largely within the framework of the UNESCO-project Flora Neotronica. The first goal is to provide a modern classification of the family as a whole, the second is the publication of a series of monographs for Flora Neotropica. The project has been planned and started in close consultation with leading botanists on the Neotropical flora. The Annonaceae are a family of pantropical distribution with between 2000 and 2500 species in ca. 130 genera as presently understood. In the Neotropics the family is represented by ca. 750 species and 35 genera. It is a family of trees, shrubs, and lianas. Its place is within the order of the Magnoliales and its supposedly closest relative is the family of the Myristicaceae. The Annonaceae, although generally considered primitive in many features, nevertheless offer a number of specialized features as well This makes it a promising object using various kinds of comparative morphological, karyological, and anatomical data. Besides, many species are of medicinal or commercial value, such as various species of Annona and Rollinia, the fruits of which are commonly eaten in most countries of Central America and South America; the Soursop (Annona muricata) is widely cultivated throughout the tropics.
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  • 99
    facet.materialart.
    Unknown
    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.383 (1972) nr.1 p.671
    Publication Date: 2015-05-08
    Description: Since the completion of Radlkofer’s monumental work on the Sapindaceae in Engler’s series “Das Pflanzenreich” 50 years have now elapsed, almost 40 since its publication. It is still the basis of virtually all taxonomic studies in the family. Some of the gerontogean genera have since been the subject of revisional work (Leenhouts 1969, 1971), but for the neogean representatives there are only some regional treatments (e.g. Rambo 1952; Barkley 1957; Reitz 1962; Soukup 1969), apart from descriptions of new taxa scattered through the literature. When studying the taxa native to Suriname in connection with the preparation of a supplement to the family treatment published previously in the “Flora of Suriname” (Uittien 1937) it soon became apparent to me that the genus Talisia was particularly incompletely known when Uittien published his account of the family, actually not much more than an extract from Radlkofer’s work. The number of species known or to be expected from Suriname proved to have doubled; this is not due to inadequateness of Uittien’s work but to much more extensive collecting. Two of the species met with since could not be identified with any species dealt with by Radlkofer or described after his time: these are described as new below. In order to establish that they were truly undescribed the descriptions and, where possible, types and/or other authentic specimens of all species described after Radlkofer were checked. A list of these follows; it may serve as a kind of bibliographic supplement to Radlkofer’s monograph. The two species marked with an asterisk have been posthumously listed in the supplement to his work.
    Repository Name: National Museum of Natural History, Netherlands
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  • 100
    facet.materialart.
    Unknown
    In:  Mededelingen van het Botanisch Museum en Herbarium van de Rijksuniversiteit te Utrecht (2352-5754) vol.397 (1972) nr.1 p.217
    Publication Date: 2015-05-08
    Description: Dicranella staphylina Whitehouse, a species recently described from Great Britain, is now recorded from Belgium, Denmark and The Netherlands. A new combination, Anisothecium staphylinum (Whitehouse) Sipman, Rubers & Riemann, is proposed. A study of the costal anatomy revealed that A. staphylinum in this respect most resembles A. rufescens.
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