2007
DOI: 10.1016/j.palaeo.2006.11.039
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How and why did the Lingulidae (Brachiopoda) not only survive the end-Permian mass extinction but also thrive in its aftermath?

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Cited by 47 publications
(37 citation statements)
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“…After the destruction of coniferous vegetation, lycopod spore plants came to dominate the land (1), and total benthic marine diversity remained relatively low until the Middle Triassic time (2). This was an unusually long delay for biotic recovery after a mass extinction (3), and the Early Triassic has therefore often been viewed as an interval when global conditions remained hostile to life (4)(5)(6). Both the terminal Permian crisis and a lesser mass extinction at the end of the Middle Permian were accompanied by a sharp negative shift of stable carbon isotopes, as recorded in limestones and organic carbon in numerous marine and terrestrial strata (reviewed by Retallack et al,ref.…”
mentioning
confidence: 99%
“…After the destruction of coniferous vegetation, lycopod spore plants came to dominate the land (1), and total benthic marine diversity remained relatively low until the Middle Triassic time (2). This was an unusually long delay for biotic recovery after a mass extinction (3), and the Early Triassic has therefore often been viewed as an interval when global conditions remained hostile to life (4)(5)(6). Both the terminal Permian crisis and a lesser mass extinction at the end of the Middle Permian were accompanied by a sharp negative shift of stable carbon isotopes, as recorded in limestones and organic carbon in numerous marine and terrestrial strata (reviewed by Retallack et al,ref.…”
mentioning
confidence: 99%
“…Lingulid fossils are found in many Permian-Triassic (shallow) marine sections (e.g. Peng et al, 2007) and the lowering of salinities in shallow marine settings and spreading anoxia provided ecological space for the lingulids (Peng et al, 2007;Rodland and Bottjer, 2001). It has been suggested that rising seawater temperatures in the Tethys resulted in strengthened monsoonal activity (e.g.…”
Section: Sea-level and Salinity Changesmentioning
confidence: 99%
“…Several studies in East Greenland have reported fluctuating abundances of acritarchs during the late Permian and Early Triassic (e.g. Balme, 1979;Piasecki, 1984;Stemmerik et al, 2001), but very few late Permian studies have documented the relative abundance of the different genera of aquatic palynomorphs (for example, Shen et al, 2013). Similar to dinocysts, acritarch morphology has been linked to environmental conditions, and acritarchs with longer processes are generally more abundant in more open marine settings (Lei et al, 2012;Stricanne et al, 2004).…”
mentioning
confidence: 99%
“…2) (Chao, 1927), Crurithyris speciosa Wang 1956, Neochonetes strophomenoides (Waagen, 1884), N. substrophomenoides (Huang, 1932), Orthothetina ruber (Frech, 1911), Spinomarginifera alpha (Huang, 1932), S. chenyaoyanensis Huang, 1932, S. sp., Tethyochonetes guizhouensis (Liao, 1980), T. soochowensis (Chao, 1928), T. wongiana (Chao, 1928) sized ('dwarfed') lingulid brachiopods are also very common (Peng et al 2007, as is the microgastropod Polygyrina assemblage (He et al 2008). Together, the thin-shelled bivalves, 'dwarfed' brachiopods and microgastropods constitute a highly distinctive low-diversity and highabundance neritic fauna of earliest Triassic age at the Zhongzai section.…”
Section: Stratigraphymentioning
confidence: 99%
“…These changes are reminiscent of morphological adjustments in some other marine invertebrate groups of Permian-Triassic age. For example, various workers have noted morphological changes in brachiopods and conodonts that have been interpreted as a response to stressful environments and the shortage of primary productivity (food supply) during the Permian-Triassic transition (Hayami 1997, Luo et al 2006, He et al 2007b, Peng et al 2007, Twitchett 2007). …”
Section: Bivalve Biostratigraphymentioning
confidence: 99%