Dictyorbitolininae Schroeder, 1990

SCHLAGINTWEIT, FELIX & RASHIDI, KOOROSH, 2021, Dictyoconella Henson, 1948, Upper Cretaceous Larger Benthic Foraminifera: A Taxonomic Revision With The Establishment Of Gusicella Gen. Nov. (Type-Species Dictyoconella Minima Henson), Acta Palaeontologica Romaniae 17 (2), pp. 3-13 : 10

publication ID

https://doi.org/ 10.35463/j.apr.2021.02.01

persistent identifier

https://treatment.plazi.org/id/03B887C2-2B48-4E61-FF0B-D33AB6ACDEF1

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Felipe

scientific name

Dictyorbitolininae Schroeder, 1990
status

 

Subfamily Dictyorbitolininae Schroeder, 1990 View in CoL (in Schroeder et al., 1990)

Remarks: Subfamily Dictyorbitolininae includes the following genera: Dictyorbitolina Cherchi & Schroeder, 1976 , Praedictyorbitolina Schroeder in Schroeder et al., 1990, Paracoskinolina Moullade, 1965 (see Schroeder in Schroeder et al., 1990) of the Lower Cretaceous, Gusicella gen. nov. of the Upper Cretaceous, and Schroedericonus Schlagintweit, 2020b of the Paleogene.

Genus Gusicella n. gen.

Type species: Dictyoconella minima Henson, 1948 View in CoL . Holotype P. 35838 in Henson (1948), stored at the Natural History Museum London (see also https://data.nhm.ac.uk).

Derivation of the name: The name is dedicated to Ivan Gusič for his numerous contributions to Mesozoic benthic foraminifera and dasycladalean algae.

Diagnosis: Finely agglutinated shell of medium conical morphology; wall thin, without any texture. Early stage with small embryo and an eccentric spire consisting of a few compressed chambers (~ half a whorl) displaying an angular margin in vertical section. Transverse section of the cone can be slightly compressed. Adult conical part with numerous rectilinear chambers subdivided into marginal and central zones separated by an undivided marginal trough. Marginal zone with several orders of beams and rafters forming a polygonal network. Main vertical partitions (beams) continuous between chambers. Central zone with pillars alternating between successive chambers; secondary deposits may be present. Marginal foramina are inclined at about 45 degrees with respect to the cone axis and form a circular row at the outer margin of the marginal trough. Multiple foramina situated in the central test part. Microspheric forms presumably broader and with convex cone base.

Comparisons: Due to the vertically alignment of the main partitions, Gusicella belongs to the Dictyorbitolininae as defined by Schroeder in Schroeder et al. (1990). Gusicella is so far the only genus of the Dictyorbitolininae reported from the Late Cretaceous Global Community Maturation Cycle of larger benthic foraminifera (e.g., Hottinger, 1997, Consorti, 2017). Dictyoconella Henson instead with its alternating vertical skeletal elements belongs to the Dictyoconinae Moullade (see discussion in Schlagintweit et al., 2016). The discreteness of Gusicella gen. nov. is given by the combined features of the initial part, and structural (exo- and endoskeleton) and foraminal features. Dictyorbitolina Cherchi and Schroeder has an apical embryo consisting of a simple protoconch and septulate deuteroconch, and alternating pillars in the central zone. It is worth noting that Dictyorbitolina was previously placed within the subfamily Orbitolininae ( Cherchi and Schroeder, 1976; Loeblich and Tappan, 1987), then transferred to the Dictyorbitolininae by Schroeder in Schroeder et al. (1990). Praedictyorbitolina Schroeder et al., 1990 has a simple embryo in eccentric position and alternating pillars in the central zone. In Paracoskinolina Moullade, 1965 , the main partitions and pillars are aligned between the consecutive chambers.

Henson (1948, p. 24–25) noted the presence of a “zone with undivided chamber space” (or marginal ridge) between the marginal (with exoskeleton) and central zones (with endoskeleton; see also Hottinger, 2006, p. 22) as also described from Dictyoconus Blanckenhorn by Davies (1930: marginal trough; see Figs. 7a View Fig , 9d View Fig ). Henson (1948, p. 26) also noted that in D. minima “the interseptal structures are sporadic and poorly defined in the central shield” (= central zone). In this context, Henson (ibidem) was obviously referring to the presence of secondarily infilled shell material as for instance reported from the Pfenderinidae Smout and Sugden or the orbitolinid Carinoconus Cherchi & Schroeder ( Loeblich and Tappan, 1987). The characteristics compared to those of the dictyoconid genera Carinoconus Cherchi & Schroeder and Dictyoconus Blanckenhorn are compiled in figure 6.

Remarks: The new compilation shows that the post- Cenomanian Upper Cretaceous Orbitolinidae consists of nine genera which in alphabetical order are: Abrardia Neumann & Damotte , Calveziconus Caus & Cornella , Dictyoconella Henson , Dictyoconus Blanckenhorn , Falsurgonina Arnaud-Vanneau , Gusicella Schlagintweit & Rashidi , Orbitolinopsis Henson , Paleodictyoconus Moullade , and Pseudorbitolina Douvillé.

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