2012
DOI: 10.1016/j.marmicro.2012.06.003
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Discorhabdus as a key coccolith genus for paleoenvironmental reconstructions (Middle Jurassic, Lusitanian Basin): Biometry and taxonomic status

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Cited by 18 publications
(9 citation statements)
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“…It is thus fairly plausible that the absence of environmental stress would naturally promote the background genetic expression of Lotharingius and the increase of its coccolith size. Such a size increase seems to follow the Cope's rule, as already proposed for different marine microorganisms (Schmidt et al, 2006;López-Otálvaro et al, 2012) and the "left wall" model (Stanley, 1973), i.e., evolution often starts near some "limiting boundary", and then diffuses away from an originally small-sized ancestor. Moreover, ecological stability would uphold a faster coccolith growth rate and the occurrence of larger coccoliths as stressed by Schmidt et al (2006), besides enhancing the population interspecific variability.…”
Section: Evolutionary Pushsupporting
confidence: 62%
See 1 more Smart Citation
“…It is thus fairly plausible that the absence of environmental stress would naturally promote the background genetic expression of Lotharingius and the increase of its coccolith size. Such a size increase seems to follow the Cope's rule, as already proposed for different marine microorganisms (Schmidt et al, 2006;López-Otálvaro et al, 2012) and the "left wall" model (Stanley, 1973), i.e., evolution often starts near some "limiting boundary", and then diffuses away from an originally small-sized ancestor. Moreover, ecological stability would uphold a faster coccolith growth rate and the occurrence of larger coccoliths as stressed by Schmidt et al (2006), besides enhancing the population interspecific variability.…”
Section: Evolutionary Pushsupporting
confidence: 62%
“…Morphometric studies of marine microfossils have been applied in the past in order to understand evolution or ecological and phenotypic responses of organisms to palaeoenvironmental changes. Although biometric studies of Jurassic coccoliths and nannoliths have already been carried out (Mattioli and Pittet, 2002;Bornemann et al, 2003;Giraud et al, 2006;Suan et al, 2008a;Suchéras-Marx et al, 2010;Tiraboschi and Erba, 2010;Fraguas and Erba, 2010;Fraguas and Young, 2011;López-Otálvaro et al, 2012), none of them addressed the morphological evolution of the Lotharingius genus, the most abundant coccolithophore taxon across Lower-Middle Jurassic sediments. Though a significant size increase in Lotharingius coccoliths across this time period has already been qualitatively acknowledged in the Lusitanian Basin (Portugal; Ferreira et al, 2015), no biometric evaluation has been made so far.…”
Section: Introductionmentioning
confidence: 99%
“…However, the taxonomy adopted by some of these authors is someway different to the one followed herein. Actually, biometric studies of Jurassic coccoliths such as those performed on the genera Similiscutum/Biscutum (de Kaenel and Bergen, 1993;Mattioli et al, 2004), Lotharingius (Mattioli, 1996;Fraguas and Young, 2011;Ferreira et al, 2017), Crepidolithus (Suchéras-Marx et al, 2010;Fraguas and Erba, 2010), Discorhabdus (López-Otálvaro et al, 2012) and Watznaueria (Giraud et al, 2006;Tiraboschi and Erba, 2010), resulted in a quantitative and partially revised taxonomy. Such a revision deeply impacts biostratigraphic studies and therefore the chronostratigraphic range of the redefined taxa should be precisely determined.…”
Section: Previous Workmentioning
confidence: 99%
“…The reference section for this subzone is Rabaçal. Discorhabdus striatus can be differentiated from D. ignotus by its larger size (>5 µm) and brighter birefringence colors (light grey) under polarizing light (López-Otálvaro et al, 2012).…”
Section: Njt3 -Crepidolithus Pliensbachensis Zonementioning
confidence: 99%
“…The Bajocian GSSP has been defined by the first occurrence of the ammonite assemblage including Hyperlioceras mundum (Buckman) and related species – H. furcatum (Buckman), Braunsina aspera Buckman, B. elegantula (Buckman) – by the onset of different calcareous nannofossil species of Watznaueria , and by an inversion from reversed to normal polarity (Henriques et al ., ). More recently, other fossil groups have been studied in detail across the GSSP, namely brachiopods (Andrade, , ), calcareous nannoplankton (Neto, ; Neto et al ., ; López‐Otálvaro et al ., ) and benthic foraminifers (Canales and Henriques, , ).…”
Section: Introductionmentioning
confidence: 99%