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Benton, M.J.1
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The plant-bearing strata of the Cape Stewart formation, Jameson Land, are Rhaetian-Hettangian (3) in age, supported by palynological analysis [K. R. Pedersen and J. J. Lund, Rev. Palaeobot. Palynol. 31, 1 (1980)]. These strata are marked by a >95% species-level turnover of megaflora resulting in two distinct floral zones: a pre-T-J boundary (Rhaetian) flora characterized by the presence of Lepidopteris species and a post-T-J boundary (Hettangian) flora marked by the presence of Thaumatopteris species. A transition zone flora occurs over 6 m of the 90-m outcrop containing elements from both floral zones and is characterized by the first occurrence of Thaumatopteris zone species and the last occurrence of >95% of Lepidopteris zone species. The beds that mark the last occurrence of Lepidopteris zone species have been used to designate the T-J boundary beds in Greenland.
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Rev. Palaeobot. Palynol.
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Pedersen, K.R.1
Lund, J.J.2
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The plant-bearing strata of the Höganas and Höör Sandstone formations, Scania, are Rhaetian-Hettangian in age (4), supported by palynological analysis [D. Guy-Ohlson, Geol. Foeren. Foerh. 103, 333 (1981)] and the presence of generically comparable megaflora to the Lepidopteris and Thaumatopteris zone flora of East Greenland (10). Transition zone flora [as in (10)] is absent in Scania.
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Beerling, D.J.1
Chaloner, W.G.2
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D. J. Beerling and W. G. Chaloner, Ann. Bot. 71, 431 (1992); D. J. Beerling, W. G. Chaloner, B. Huntley, J. A. Pearson, M. J. Tooley, Proc. R. Soc. London. B Biol. Sci. 251, 133 (1993); J. Van der Burgh, J. Visscher, H. Dilcher, W. M. Kurschner, Science 260, 1788 (1993); P. K. Van de Water, S. W. Leavitt, J. L. Betancourt, ibid. 264, 239 (1994); J. C. McElwain, Philos. Trans. R. Soc. London B 353, 83 (1998).
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Beerling, D.J.1
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Tooley, M.J.5
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D. J. Beerling and W. G. Chaloner, Ann. Bot. 71, 431 (1992); D. J. Beerling, W. G. Chaloner, B. Huntley, J. A. Pearson, M. J. Tooley, Proc. R. Soc. London. B Biol. Sci. 251, 133 (1993); J. Van der Burgh, J. Visscher, H. Dilcher, W. M. Kurschner, Science 260, 1788 (1993); P. K. Van de Water, S. W. Leavitt, J. L. Betancourt, ibid. 264, 239 (1994); J. C. McElwain, Philos. Trans. R. Soc. London B 353, 83 (1998).
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Science
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Van Der Burgh, J.1
Visscher, J.2
Dilcher, H.3
Kurschner, W.M.4
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D. J. Beerling and W. G. Chaloner, Ann. Bot. 71, 431 (1992); D. J. Beerling, W. G. Chaloner, B. Huntley, J. A. Pearson, M. J. Tooley, Proc. R. Soc. London. B Biol. Sci. 251, 133 (1993); J. Van der Burgh, J. Visscher, H. Dilcher, W. M. Kurschner, Science 260, 1788 (1993); P. K. Van de Water, S. W. Leavitt, J. L. Betancourt, ibid. 264, 239 (1994); J. C. McElwain, Philos. Trans. R. Soc. London B 353, 83 (1998).
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(1994)
Science
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Van De Water, P.K.1
Leavitt, S.W.2
Betancourt, J.L.3
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24
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D. J. Beerling and W. G. Chaloner, Ann. Bot. 71, 431 (1992); D. J. Beerling, W. G. Chaloner, B. Huntley, J. A. Pearson, M. J. Tooley, Proc. R. Soc. London. B Biol. Sci. 251, 133 (1993); J. Van der Burgh, J. Visscher, H. Dilcher, W. M. Kurschner, Science 260, 1788 (1993); P. K. Van de Water, S. W. Leavitt, J. L. Betancourt, ibid. 264, 239 (1994); J. C. McElwain, Philos. Trans. R. Soc. London B 353, 83 (1998).
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McElwain, J.C.1
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0344825581
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note
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Primary SD and SI data (Table 1) were normalized according to x̄ - x, where x̄ is the genus mean for all beds or localities in either Greenland or Sweden and x is the genus mean per bed or locality. Normalized data were then corrected for any shifts in floral composition between individual beds by multiplying by the percentage composition of that genus at each of the beds or localities in Sweden and Greenland. These procedures were repeated for all individual genera to calculate an artificially genus-weighted trend. Mean genus-weighted SD and SI trends were calculated for both sites and removed from the normalized data to provide detrended stomatal records, which were independent of any floral composition changes between individual beds or localities.
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30
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0033556495
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2) where ΔT is the difference in mean global surface air temperature. The estimates will be somewhat dependent on the responses of the thermohaline circulation [E. Barrera et al., Geology 25, 715 (1997)].
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Geophys. Res. Lett.
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Kothavala, Z.1
Oglesby, R.J.2
Saltzman, B.3
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31
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0031448788
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2) where ΔT is the difference in mean global surface air temperature. The estimates will be somewhat dependent on the responses of the thermohaline circulation [E. Barrera et al., Geology 25, 715 (1997)].
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(1997)
Geology
, vol.25
, pp. 715
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Barrera, E.1
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32
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0021556306
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2 [J. L. Sarmiento and J. R. Toggweiler, Nature 308, 621 (1984)]. Isotopic evidence supports a reduction in oceanic productivity at the T-J boundary (8); however, the data are equivocal because of potential diagenetic effects (8, 9).
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(1984)
Nature
, vol.308
, pp. 621
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Sarmiento, J.L.1
Toggweiler, J.R.2
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35
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0029505149
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-1) and close to daily maximum temperatures are reached. This approach was used to estimate relative maximum leaf size during the period of study (Fig. 3).
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(1995)
Global Change Biol.
, vol.1
, pp. 289
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Beerling, D.J.1
Quick, W.P.2
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36
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0001148592
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E. D. Schultze and M. M. Caldwell, Eds. Springer-Verlag, Berlin
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The threshold for thermal damage of nonsucculent leaves (45° to 52°C) is a highly conserved characteristic across a wide range of extant taxa [W. Larcher, in Ecophysiology of Photosynthesis, E. D. Schultze and M. M. Caldwell, Eds. (Springer-Verlag, Berlin, 1994), pp. 261-277; Y. Gauslaa, Holarct. Ecol. 7, 1 (1984)], implying little evolutionary change through time.
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(1994)
Ecophysiology of Photosynthesis
, pp. 261-277
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Larcher, W.1
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37
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0021576203
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The threshold for thermal damage of nonsucculent leaves (45° to 52°C) is a highly conserved characteristic across a wide range of extant taxa [W. Larcher, in Ecophysiology of Photosynthesis, E. D. Schultze and M. M. Caldwell, Eds. (Springer-Verlag, Berlin, 1994), pp. 261-277; Y. Gauslaa, Holarct. Ecol. 7, 1 (1984)], implying little evolutionary change through time.
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(1984)
Holarct. Ecol.
, vol.7
, pp. 1
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Gauslaa, Y.1
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39
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0345256853
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A review of fossil Ginkgoalean leaves revealed that species with the most dissected leaves, characterized by multidichotomies 0.5 to 2 mm wide, are restricted to Late Triassic to early Middle Jurassic facies [T. Kimura, G. Naito, T. Ohana, Bull. Natl. Sci. Mus. Tokyo 9, 91 (1983)].
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(1983)
Bull. Natl. Sci. Mus. Tokyo
, vol.9
, pp. 91
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Kimura, T.1
Naito, G.2
Ohana, T.3
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40
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84879883424
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The cause of T-J floral turnover has traditionally been attributed to a sedimentary hiatus (3). However, this hypothesis is unsupported by sedimentological evidence [G. Dam and F. Surlyk, Geology 20, 749 (1992); Spec. Publ. Int. Assoc. Sedimentol. 18, 4189 (1993)], which identifies no major facies changes or unconformities between the T-J strata in Greenland. Furthermore, the absence of the upper Rhaetian Ricciisporites-Polypodisporites acme zone [W. M. L. Schuurman, Rev. Palaeobot. Palynol. 23, 159 (1977)] in Greenland (10) and Sweden (11), which has also been tentatively interpreted as evidence of a hiatus at both localities, is questionable, as acme zones are generally considered of only local use, owing to the effects of ecological, environmental, and postdepositional processes on relative pollen abundances.
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(1992)
Geology
, vol.20
, pp. 749
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Dam, G.1
Surlyk, F.2
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41
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0344394005
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The cause of T-J floral turnover has traditionally been attributed to a sedimentary hiatus (3). However, this hypothesis is unsupported by sedimentological evidence [G. Dam and F. Surlyk, Geology 20, 749 (1992); Spec. Publ. Int. Assoc. Sedimentol. 18, 4189 (1993)], which identifies no major facies changes or unconformities between the T-J strata in Greenland. Furthermore, the absence of the upper Rhaetian Ricciisporites-Polypodisporites acme zone [W. M. L. Schuurman, Rev. Palaeobot. Palynol. 23, 159 (1977)] in Greenland (10) and Sweden (11), which has also been tentatively interpreted as evidence of a hiatus at both localities, is questionable, as acme zones are generally considered of only local use, owing to the effects of ecological, environmental, and postdepositional processes on relative pollen abundances.
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(1993)
Spec. Publ. Int. Assoc. Sedimentol.
, vol.18
, pp. 4189
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42
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0000610607
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The cause of T-J floral turnover has traditionally been attributed to a sedimentary hiatus (3). However, this hypothesis is unsupported by sedimentological evidence [G. Dam and F. Surlyk, Geology 20, 749 (1992); Spec. Publ. Int. Assoc. Sedimentol. 18, 4189 (1993)], which identifies no major facies changes or unconformities between the T-J strata in Greenland. Furthermore, the absence of the upper Rhaetian Ricciisporites-Polypodisporites acme zone [W. M. L. Schuurman, Rev. Palaeobot. Palynol. 23, 159 (1977)] in Greenland (10) and Sweden (11), which has also been tentatively interpreted as evidence of a hiatus at both localities, is questionable, as acme zones are generally considered of only local use, owing to the effects of ecological, environmental, and postdepositional processes on relative pollen abundances.
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(1977)
Rev. Palaeobot. Palynol.
, vol.23
, pp. 159
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Schuurman, W.M.L.1
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43
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0345256852
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note
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std)] - 1} × 1000 where unk the ratio of unknown to sample and std is the ratio of the pee dee belemnite standard.
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45
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0344394004
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note
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13C. We gratefully acknowledge funding from the Natural Environment Research Council, UK (GR9/02930), and through Royal Society Research Fellow and Equipment grants to D.J.B.
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