2017
DOI: 10.1016/j.revmic.2017.08.002
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Late Ordovician (Katian) chitinozoans from northwest Saudi Arabia: Biostratigraphic and paleoenvironmental implications

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Cited by 10 publications
(14 citation statements)
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“…The success of the egg hypothesis is mainly owing to the hermetically sealed vesicle which restricts communication between the inner chamber and the outer environment, and the cocoon-like clustered specimens. However, among the 57 recognized chitinozoan genera [48,49], the cocoon-like clusters have only been observed in a single genus— Desmochitina [19,28]. Furthermore, the cocoon-like preservation could also make sense to be interpreted as a reproduction stage, for instance, a multiple fission stage of an individual organism.…”
Section: Discussionmentioning
confidence: 99%
“…The success of the egg hypothesis is mainly owing to the hermetically sealed vesicle which restricts communication between the inner chamber and the outer environment, and the cocoon-like clustered specimens. However, among the 57 recognized chitinozoan genera [48,49], the cocoon-like clusters have only been observed in a single genus— Desmochitina [19,28]. Furthermore, the cocoon-like preservation could also make sense to be interpreted as a reproduction stage, for instance, a multiple fission stage of an individual organism.…”
Section: Discussionmentioning
confidence: 99%
“…This interval consists of olive-grey siltstone, fine-grained sandstone, dark shale, and brown impure limestone interbeds, which contain graptolites, identified as Orthograptus amplexicaulis (Ghavidel-Syooki 2001), indicating a Late Ordovician (Katian) age ( clingani to acceps zone), providing additional age control. It has also been recorded from the upper Caradoc (lower Katian) of the Algerian Sahara (Taugourdeau and de Jekhowsky 1960), Morocco (Bourahrouh et al 2004), upper Caradoc (lower Katian), Ra'an Member of the Qasim Formation, Arabian Peninsula (Al-Hajri 1995; Paris et al 2000b; Al-Shawareb et al 2017), upper Caradoc (lower Katian), Turkey (Paris et al 2007), upper Caradoc (lower Katian) of Iran (Ghavidel-Syooki 2001, 2017; Ghavidel-Syooki and Winchester-Seeto 2002; Ghavidel-Syooki and Piri-Kangarshahi 2021) and the Hirnantian, Baq'a Shale Member of the Sarah Formation, Arabian Peninsula (Paris et al 2015). Tanuchitina fistulosa is well-preserved and abundant in the Seyahou Formation (interval samples MG-21 to MG-33), similar to that of the Ra'an Member of the Qasim Formation in the Arabian Peninsula (Paris et al 2000b).…”
Section: Biostratigraphy Of the Chitinozoan Faunasmentioning
confidence: 97%
“…Other chitinozoan taxa in this biozone consist of Calpichitina lenticularis (Bouché 1965), Lagenochitina baltica (Eisenack 1931), Acanthochitina pudica (Vandenbroucke 2008), Pistillachitina pistillifrons (Eisenack 1939), Hyalochitina hyalophrys (Eisenack 1959), Pistillachitina comma (Eisenack 1959), and Rhabdochitina usitata (Jenkins 1967). Amongst these chitinozoan taxa, Rhabdochitina usitata ranges from Middle to Late Ordovician (Darriwilian–Sandbian; see Jenkins 1967), but the others are classical components of the Late Ordovician (late Caradoc) in the North Gondwana Domain (Al-Hajri 1995; Oulebsir and Paris 1995; Ghavidel-Syooki 2001; Ghavidel-Syooki and Winchester-Seeto 2002; Ghavidel-Syooki 2008; Ghavidel-Syooki et al 2011a, 2011b; Paris et al 2015; Ghavidel-Syooki 2016; Al-Shawareb et al 2017; Ghavidel-Syooki 2017; Ghavidel-Syooki and Piri-Kangarshahi 2021).…”
Section: Biostratigraphy Of the Chitinozoan Faunasmentioning
confidence: 99%
“…Chitinozoans are organic-walled microfossils common in Ordovician to Devonian marine sediments. In spite of their disputed biological origin (see Liang et al, 2020a and references therein), chitinozoans are widely used in biostratigraphy of early and middle Paleozoic rocks (e.g., Grahn and Gutiérrez, 2001; Asselin et al, 2004; Vandenbroucke, 2004; Grahn, 2005a; Steemans et al, 2009; Vandenbroucke et al, 2010, 2015; de la Puente and Rubinstein, 2013; Wang et al, 2013; Paris et al, 2015a, b; Al-Shawareb et al, 2017; De Weirdt et al, 2019; Liang et al, 2020b) since the regional and global biozonal schemes were first established around the 1990s (Achab, 1989; Paris, 1990; Nõlvak and Grahn, 1993; Verniers et al, 1995; Paris et al, 2004; Grahn, 2005b, 2006). However, alongside revised genus- and family-level systematics (Paris et al, 1999), and continuously expanding datasets from different regions in recent years, revisions of several well-known taxa are required.…”
Section: Introductionmentioning
confidence: 99%