2010
DOI: 10.1134/s0031030110100072
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A new Bennettitalean genus from the Middle Jurassic of the Mikhailovskii Rudnik locality (Kursk Region, Russia)

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Cited by 7 publications
(4 citation statements)
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“…Finally, encryption of stomata in deep abaxial trichome‐filled grooves or chambers occurred in various extinct plant groups (e.g., noeggerathiopsid and rufloriacean cordaitaleans, Dicranophyllales, williamsoniacean Bennettitales and high‐latitude cheirolepidacean conifers) that characterized humid and even peat‐forming environments in the late Paleozoic and Mesozoic (e.g., Meyen, 1963; Alvin, 1982; Meyen and Smoller, 1986; McLoughlin and Drinnan, 1996; Villar de Seoane, 2001; Gordenko and Broushkin, 2010; Tosolini et al, 2014). Although clearly not subject to genuinely arid climates, these plants may have experienced high levels of water stress due to growth in areas of sustained winds or on acidic or low‐nutrient substrates, especially under locally seasonal climates (Haworth and McElwain, 2008; Pott et al, 2008; Pott and McLoughlin, 2009).…”
Section: Discussionmentioning
confidence: 99%
“…Finally, encryption of stomata in deep abaxial trichome‐filled grooves or chambers occurred in various extinct plant groups (e.g., noeggerathiopsid and rufloriacean cordaitaleans, Dicranophyllales, williamsoniacean Bennettitales and high‐latitude cheirolepidacean conifers) that characterized humid and even peat‐forming environments in the late Paleozoic and Mesozoic (e.g., Meyen, 1963; Alvin, 1982; Meyen and Smoller, 1986; McLoughlin and Drinnan, 1996; Villar de Seoane, 2001; Gordenko and Broushkin, 2010; Tosolini et al, 2014). Although clearly not subject to genuinely arid climates, these plants may have experienced high levels of water stress due to growth in areas of sustained winds or on acidic or low‐nutrient substrates, especially under locally seasonal climates (Haworth and McElwain, 2008; Pott et al, 2008; Pott and McLoughlin, 2009).…”
Section: Discussionmentioning
confidence: 99%
“…from the Middle Jurassic of Yorkshire, U.K. (Cleal & Rees 2003, Cleal et al 2006, Pott et al 2007, Zhao et al 2018, appears to lack trichomes or trichome bases, but these are very common among other Nilssoniopteris species (see Na et al 2014, Ray et al 2014 as well as in other genera of bennettitalean leaves (e.g. Sincock & Watson 1988, Watson & Sincock 1992, Boyd 2000, Gordenko & Broushkin 2010, Pott et al 2012. The trichome bases are typically one-or two-celled (rarely three-celled or more) and may be very sparse or abundant, and all appear very similar in morphology at high magnification under SEM (e.g.…”
Section: Palaeoecological Considerationsmentioning
confidence: 99%
“…Sympterophyllum is described as having what appear to be fused segments of lamina. The description of S. sympinnatum does not indicate that the adaxial surface is corrugated, but the leaf is reconstructed with each segment being adaxially convex, producing a corrugated configuration (Gordenko and Broushkin, 2010, fig. 1).…”
mentioning
confidence: 99%
“…As the result of the typically disarticulated nature of plant remains in the fossil record we do not yet have evidence for predicting to which, if either, of the seed cones N. corrugata belongs. Nevertheless, the distribution of the genus Nillsoniopteris in the fossil record reveals that plants with leaves of this type had extremely wide global diversity (i.e., 50 species) throughout the Mesozoic (Table 1; Taylor et al, Gordenko andBroushkin, 2010 2009). Because more than one species of bennettitalean remains characterize a large percentage of fossil plant assemblages that are preserved throughout their geologic range (e.g., references in Table 1), it is clear that bennettitalean plants were a major component of global vegetation for nearly 180 million years.…”
mentioning
confidence: 99%