Neokilianina, 1988

Schlagintweit, Felix, 2023, Neokilianina Concava Ramalho, 2015 And Neokilianina Rahonensis (Foury & Vincent, 1967): A Dimorphic Pair Of Upper Jurassic Larger Benthic Foraminifera?, Acta Palaeontologica Romaniae 19 (2), pp. 15-17 : 15

publication ID

https://doi.org/ 10.35463/j.apr.2023.02.02

DOI

https://doi.org/10.5281/zenodo.10974269

persistent identifier

https://treatment.plazi.org/id/E6659F32-FF85-FFC4-FF14-E5E3DC46F852

treatment provided by

Felipe

scientific name

Neokilianina
status

 

THE CASE STUDY OF NEOKILIANINA RAHONENSIS View in CoL ( FOURY & VINCENT, 1967) AND NEOKILIANINA CONCAVA RAMALHO, 2015

Generalities

The genus Neokilianina Septfontaine (type-species Kilianina rahonensis Foury & Vincent, 1967 ), not included in the recent classification of agglutinated foraminifera ( Kaminski, 2014), is considered a valid genus ( Schlagintweit, 2014; Septfontaine, 2020). The taxonomic history respectively has been summarized by Schlagintweit (2014, p. 28) as follows: ‘ In an abstract for the Benthos ´86 Meeting in Geneva, Septfontaine (1986) excluded it from the genus Kilianina and assigned it to a new taxon Neokilianina n. gen. Loeblich and Tappan (1987: p. 721) treated Neokilianina as invalid, since in the abstract of Septfontaine (1986) no description was provided and no type species was designated. The topic of the Geneva abstract was published two years after the meeting introducing Neokilianina rahonensis ( Septfontaine, 1988, p. 249) . As type species Septfontaine (1988: p. 249) explicitely named Kilianina rahonensis and concerning the description reference was made to that given by Foury and Vincent (1967).’ The reference to Foury & Vincent (1967) however needs to be corrected as the morphology of ‘ Kilianina ’ rahonensis has been originally described as orbitoliniform with uniserial adult chambers that follow the trochospirally coiled early stage. The genus Neokilianina has been assigned by Septfontaine (1988) to the family Valvulinidae Berthelin, 1880 , subfamily Parurgonininae Septfontaine, 1988 with trochospirally coiled chambers throughout ontogeny. It comprises the two species Neokilianina (ex Kilianina ) rahonensis ( Foury & Vincent, 1967) from the Kimmeridgian of France and N. concava Ramalho, 2015 from the Kimmeridgian of Portugal. It is worth mentioning that the stratigraphic distribution of N. rahonensis comprises the uppermost Oxfordian to lowermost Tithonian interval ( Pleş et al., 2019).

Taxonomic interpretation

In the description and diagnosis of the new species Neokilianina concava , occurring in the same (isochronous) levels with N. rahonensis, Ramalho (2015, p. 41) stressed the two main specific characteristics of the external morphology as a greater apical angle and a conspicuous basal concavity. ‘ Both species exhibit the same type of internal structure ’ ( Ramalho, 2015, p. 42). Herein, it is suggested to not consider them as two different species but instead as a dimorphic pair as reported from various other Jurassic-Cretaceous larger benthic foraminifera. A well-known cross-reference for example is represented by the (Lower) Cretaceous trocho- to uniserial Orbitolinidae Martin, 1890 (e.g., Hofker, 1966). Examples of the much rarer microspheric forms displaying wider apical cone angles along with greater test diameter, often also with a central concave depression at the base and including final annular chambers include the genera Neorbitolinopsis Schroeder, 1964 ( Berthou & Schroeder, 1978), Montseciella Cherchi & Schroeder (1999) ( Schroeder et al., 2010; this work), or Calveziconus Caus & Cornella, 1981 ( Fig. 1 View Fig a-d). An equivalent interpretation can be applied to the two morphotypes of Neokilianina with N. rahonensis referring to the high-conical specimens described by Foury & Vincent (1967) as the megalospheric form ( Fig. 1g View Fig ) and the low-conical N. concava as the microspheric form ( Fig. 1h View Fig ). The fact that the latter occurs in the same levels as forms designated as N. rahonenensis and that there are no internal structural differences between both supports such a conclusion. The co-occurrence of both morphotypes seems to exclude an interpretation as ecomorphotypes (difference on test shape given by adaptation to different ecological variables). With the preferred interpretation, the genus Neokilianina Septfontaine becomes reduced to its sole type-species N. rahonensis (Foury & Vincent) . Although Foury & Vincent (1967, p. 39) mention two morphological different types that might be related to different generations, all of the illustrated specimens have been referred to high-conical megalospheric specimens and also the diameter-height diagram illustrated in figure 5 therein does not show two discriminatory fields. In addition, details about morphological and dimensional differences have not been provided and do therefore not allow further comments. Foury & Vincent (1967, p. 40) reported a biloculine embryo consisting of a spherical protoconch enveloped by the deuteroconch and situated at the apex of the test. It is followed by 5 to 6 whorls of ‘helicospiral’ chambers (= informal praevalvulinid stage sensu Septfontaine, 2020). The megalospheric embryo has neither been illustrated by Foury & Vincent (1967) nor have dimensions been provided. Details on the proloculi of the two generations are therefore still pending, so that the observed dimorphism refers to the adult test morphologies. Finally, it should be mentioned, that an equivalent dimorphism as in Neokilianina rahonensis as assumed herein has been illustrated by Foury & Vincent (1967) from the middle Jurassic species Kilianina blancheti Pfender, 1933 ( Fig. 1 View Fig e-f).

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