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branch abscission

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Journal Article
Journal: Paleobiology
Published: 25 February 2013
Paleobiology (2013) 39 (2): 235–252.
...Cindy V. Looy Abstract Within conifers, active abscission of complete penultimate branch systems is not common and has been described mainly from juveniles. Here I present evidence for the abscission of penultimate branch systems within early so-called walchian conifers—trees with a plagiotropic...
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Diagram showing an  Araucaria australis  <span class="search-highlight">branch</span> before and after <span class="search-highlight">abscission</span>...
Published: 25 February 2013
Figure 2.  Diagram showing an Araucaria australis branch before and after abscission. The xylem (black) is strongly reduced close to the base of the branch. Prior to abscission, expansion of the cortex and central pith (gray) leads to an enlarged base diameter near the abscission zone
Journal Article
Published: 01 January 2001
Geological Magazine (2001) 138 (1): 39–52.
...H. J. FALCON-LANG; D. J. CANTRILL Abstract The leaf longevity and seasonal timing of leaf abscission within a plant community is closely related to climate, a phenomenon referred to as leaf phenology. In this paper the leaf phenology of some mid-Cretaceous (late Albian) forests which grew...
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Walchian conifer <span class="search-highlight">branch</span> systems and <span class="search-highlight">branch</span> bases from Colwell Creek Pond. T...
Published: 25 February 2013
Figure 3.  Walchian conifer branch systems and branch bases from Colwell Creek Pond. The fossils are preserved as three-dimensional reddish-brown goethite petrifactions in pink-reddish mudstones. Note the smooth abscission surfaces in all specimens, and pattern of penultimate leaf bases
Image
Bases of walchian conifer <span class="search-highlight">branch</span> systems from Colwell Creek Pond (upper two...
Published: 25 February 2013
the different morphotypes in distance between the first ultimate shoots and the branch base; also note the smooth abscission surfaces of the swollen branch bases. A–J, NMNH specimens (USNM 539423 (A), 530990 (B), 530991 (C), 539433 (D), 530937 (E), 531003 (F), 530993 (G), 531007 (H), 536456 (I), 531004 (J). K–M
Journal Article
Journal: PALAIOS
Published: 01 October 2005
PALAIOS (2005) 20 (5): 418–428.
... in the fossil record could be confused with traumatically removed branches when, indeed, this condition is a physiological response. Abscissed leaves tend to fall with their convex surface facing downwards ( Ferguson, 1995 ; Gastaldo et al., 1996 ; Martín-Closas and Gomez, 2004 ). This phenomenon, when...
Journal Article
Journal: Lithosphere
Publisher: GSW
Published: 01 December 2021
Lithosphere (2021) 2021 (Special 4): 2860087.
... in the western China. The SBBM working face was divided into several blocks according to the size of the mining area; protective coal pillars with certain widths were set between the adjacent blocks. Each block was divided into multiple recoveries of coal pillars to be mined by arranging branch roadways...
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Journal Article
Published: 01 March 2001
Journal of Paleontology (2001) 75 (2): 449–460.
... to result from compression of a thick lamina. These falcate ribbon-like organs may be pinnae of a pinnately compound cycad-like frond. If pinnae, the square base suggests that the pinnae were inserted perpendicularly, rather than obliquely, and broke away by abscission, as seen in some modern cycads. Among...
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Journal Article
Published: 01 May 2007
Journal of Paleontology (2007) 81 (3): 550–567.
... or truncate, pinnatasect pinnules. The initial description of the tenuinervis -type was later emended to include an expanded petiole base that is truncated by an inferred abscission layer which shows a ring of vascular strands ( Halle, 1913 ; Harris, 1964 ). Though these two leaf types differ...
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Journal Article
Published: 01 May 2000
Geological Magazine (2000) 137 (3): 257–268.
..., specimen no. ICN-PI-0268-1; (h) fertile branching axes, specimen no. ICN-PI-0380-1; (i) fertile branching axes showing bifurcate and trifurcate (arrows) branching, specimen no. ICN-PI-0327. Scale bars: (a) 10 mm, (b–d) 2 mm, (e, f) 5 mm, (g–i) 10 mm. Figure 4. Colpodexylon cf. deatsii Banks...
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Journal Article
Published: 28 November 2016
Journal of Paleontology (2017) 91 (1): 1–11.
...Steven T. LoDuca; Denis K. Tetreault Abstract The thallus of a new noncalcified dasycladalean alga, Wiartonella nodifera n. gen. n. sp., from the mid-Silurian Eramosa Lagerstätte of Ontario, Canada, comprises a narrow main axis with laterals in whorls (euspondyl). Laterals branch to the second...
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Journal Article
Published: 01 March 2010
Journal of Sedimentary Research (2010) 80 (3): 268–287.
.... 7A ), suggestive of branches and/or small trunks, and the longest is 1.25 m long. Sigillaria is common, and lepidodendroids are also present. Arborescent lycopsids had a pole-like architecture, and in many forms a reproductive crown of branches arose just prior to death ( Phillips and DiMichele...
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Journal Article
Published: 22 January 2015
Journal of the Geological Society (2015) 172 (2): 175–185.
... . Labandeira C.C. Johnson K.R. Wilf P. 2002 . Impact of the terminal Cretaceous event on plant–insect associations . Proceedings of the National Academy of Sciences of the USA , 99 , 2061 – 2066 . Looy C.V. 2013 . Natural history of a plant trait: Branch system abscission...
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Series: Geological Society, London, Special Publications
Published: 29 July 2022
DOI: 10.1144/SP521-2021-122
EISBN: 9781786205834
... by a scale (arrows). The scale bar is 0.1 mm. ( d ) Branch with helically arranged decurrent leaf scars (arrows). The scale bar is 1 mm. ( e ) Decurrent leaf base (arrow) with abscission zone at the tip. The scale bar is 0.1 mm. ( f ) Subtending scale (below the line) and an axillary primordium (arrow...
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Journal Article
Published: 10 May 2016
Bulletin of the Seismological Society of America (2016) 106 (3): 1125–1132.
... between the zone expressed as the absciss along the x axis is a translation of the uniform distribution in angle theta. After determining the area as a function of R and θ , the prior of x lim is expressed as Ultimately, what we need is the marginal probability of the limit itself; therefore...
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Journal Article
Journal: PALAIOS
Published: 01 November 2012
PALAIOS (2012) 27 (11): 765–778.
... in the vertical section of the ditch could thus be determined. After the blocks had been transported to, and dried out in, the laboratory, they were split into several smaller hand specimens. Plant remains (leaves, leafy shoots, cone scales, fragments of branches, woody debris) were exposed on all bedding...
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Journal Article
Published: 01 August 2016
Journal of Sedimentary Research (2016) 86 (8): 944–964.
.... 2013 , Natural history of a plant trait: branch-system abscission in Paleozoic conifers and its environmental, autecological, and ecosystem implications in a fire-prone world : Paleobiology , v. 39 , p. 235 – 252 . Looy...
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Journal Article
Published: 01 March 2002
Journal of Paleontology (2002) 76 (2): 347–376.
..., dichotomous branching, fragmentation along pre-formed abscission surfaces, and wart-like conceptacles collectively distinguish this population and support its possible placement among the fucalean brown algae. Whatever their affinities, these small, ribbon-shaped fossils are the most abundant constituents...
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Journal Article
Journal: PALAIOS
Published: 30 October 2023
PALAIOS (2023) 38 (10): 407–435.
...: Lebowskia gen. nov. (Majoniaceae ): International Journal of Plant Sciences , v. 168 , p. 957 – 972 . doi: 10.1086/518256 . Looy, C.V. 2013 , Natural history of a plant trait: branch-system abscission in Paleozoic conifers and its environmental, autecological...
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Journal Article
Journal: PALAIOS
Published: 01 March 2013
PALAIOS (2013) 28 (3): 163–177.
... were missing. Although five species of palms (four trees and one vine) were present in the Noah Creek plot, only fragments of the vine Calamus occurred in the leaf litter samples. The absence of palm leaves from the leaf litter is explained by their differing leaf abscission process. For the palms...
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