2007
DOI: 10.1016/j.palaeo.2006.10.015
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Minimal insect herbivory for the Lower Permian Coprolite Bone Bed site of north-central Texas, USA, and comparison to other Late Paleozoic floras

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Cited by 75 publications
(93 citation statements)
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“…The Bletterbach damage frequency (3.5%) is comparable, within a factor of three, to analyses of bulk floral damage values on coeval palaeofloras from Euramerica (Beck and Labandeira, 1998;Labandeira and Allen, 2007;Vasilenko, 2007), Cathaysia (Glasspool et al, 2003), and other Gondwanan sites (e.g., Adami-Rodrigues et al, 2004a, 2004bPrevec et al, 2009;Gallego et al, 2014). Consequently, the Bletterbach level of overall herbivory is typical for Permian wetland floras.…”
Section: Plant-insect Interactionssupporting
confidence: 62%
“…The Bletterbach damage frequency (3.5%) is comparable, within a factor of three, to analyses of bulk floral damage values on coeval palaeofloras from Euramerica (Beck and Labandeira, 1998;Labandeira and Allen, 2007;Vasilenko, 2007), Cathaysia (Glasspool et al, 2003), and other Gondwanan sites (e.g., Adami-Rodrigues et al, 2004a, 2004bPrevec et al, 2009;Gallego et al, 2014). Consequently, the Bletterbach level of overall herbivory is typical for Permian wetland floras.…”
Section: Plant-insect Interactionssupporting
confidence: 62%
“…Until the Mid-Lower Cretaceous these traces were described on gymnosperms (Medullosales, Gingantopteridales, Cordaitales, Cycadales, Peltaspermales, Glossopteridales, Ginkgoales) and Sphenopsids, predominately from the Northern Hemisphere (North America and Europe), by Ash (1972Ash ( , 1997, Castro (1997), Grauvogel-Stamm & Kelber (1996), Beck & Labandeira (1998), Labandeira (2006), Trout et al (2000), Glasspool et al (2003), Labandeira & Allen (2007), Vasilenko (2007a). Moreover, there are a few preCretaceous records in South America that include circular to slot holes on Cordaites, Gangamopteris McCoy, 1875 and Glossopteris leaves from the Lower Permian of Brazil (Adami-Rodrigues et al, 2004;De Souza Pinheiro et al, 2012); circular to elliptical hole feeding traces in Glossopteris wilsonii Seward, 1914 andGinkgoites eximia Feruglio, 1942 from the Early Permian of Argentina (Gallego et al, 2014); hole and marginal feeding, leaf-mines and skeletonizations in different plant species from Middle-Late Triassic of Argentina (Adami-Rodrigues et al, 2012) and hole feeding on leaves of Taeniopteris sp.…”
Section: A B 231 Robledo Et Al -Phytophagy On Fossil Ferns From Argementioning
confidence: 99%
“…from the Lower Permian (Asselian) of Chemnitz, in the Erzgebirge Basin of Germany; however, he did not find larger, insect-like coprolites in the cortical parenchyma, as in Pennsylvanian-age specimens from the United States. By contrast, Permian compression-impression record from north-central Texas had fewer instances of detritivorous and herbivorous associations, and consumption of Psaronius-affiliated Pecopteris foliage either was virtually absent in the case of the Lower Permian (late Sakmarian) Coprolite Bone Bed Flora (Labandeira and Allen, 2007), or occurs at (very) low levels in other, similarly aged Texan floras that have been preliminarily studied (Beck and Labandeira, 1998). Notably, it is the seed plants, particularly medullosan and gigantopterid pteridosperms, that overwhelmingly display the highest herbivory levels in these compression floras (Labandeira, 2006a).…”
Section: Introductionmentioning
confidence: 92%
“…Stoval and Strain (1936) described Paleogene fecal structures, referred to a mammalian origin. This brief survey of coprolites from the late Palaeozoic to more recent occurrences clearly indicates that plant-animal associations have an ancient history, and were relatively abundant in late Paleozoic deposits, both as generalized detritivory but also as more specialized and highly varied types of herbivory (Kevan et al, 1975;Scott, 1977;Scott and Taylor, 1983;Labandeira, 2002;Labandeira and Allen, 2007).…”
Section: Introductionmentioning
confidence: 98%