Novalesia producta ( Magniez, 1972 ), 2025

Schlagintweit, Felix & Rashidi, Koorosh, 2025, Novalesia Producta (Magniez, 1972), A Little-Known Benthic Foraminifer From The Aptian Taft Formation Of Central Iran, Acta Palaeontologica Romaniae 21 (1), pp. 81-88 : 84-86

publication ID

https://doi.org/10.35463/j.apr.2025.01.05

persistent identifier

https://treatment.plazi.org/id/03C087C0-FFF8-FFE8-2991-FF39331DFEFC

treatment provided by

Felipe

scientific name

Novalesia producta ( Magniez, 1972 )
status

 

Novalesia producta ( Magniez, 1972) View in CoL

Figs. 2E View Fig , 3 View Fig

*1972 Spiroplectamminoides productus sp. nov. – Magniez, pl. 1, figs. 1-13, pl. 4, figs. 1-12, fig. 3.

1974 Novalesia producta (Magniez) gen. et comb. nov. – Magniez, p. 155.

1980 Novalesia producta (Magniez) – Arnaud-Vanneau, p. 538, pl. 44, figs. 3-5, pl. 69, figs. 11-15, text-figs. 197- 198.

1995 Novalesia producta (Magniez) – Arnaud-Vanneau & Sliter, p. 551, pl. 1, fig. 8.

1995 Novalesia producta (Magniez) – Kirmaci et al., pl. 5, figs. 7-10.

1995 Novalesia producta (Magniez) – Koch et al., pl. 1, fig. 10.

2011 Pseudotextulariella cf. scarselai (De Castro) – Roozbahani, pl. 2, fig. 10.

Non 2015 Novalesia producta (Magniez) – Madhavaraju et al., 1-4 (= bi- or triserial agglutinated taxon with simple chambers), 5 (possible).

?2016 Novalesia producta (Magniez) – Yavari et al., fig. 4F.

Non 2016 Novalesia cf. producta (Magniez) – Hemmati et al., pl. 3, fig. 15 (= bi- or triserial agglutinated taxon with simple chambers).

2022 Praechrysalidina infracretacea – Hassani, fig. 9.5.

Description: Test elongate, conical, and slightly compressed (~cylindroconical) ( Figs. 3 View Fig C-D). Cross sections are oval to nearly circular. The subspherical proloculus is followed by an early planispirally coiled stage, about half a whorl, that comprises three to six chambers (e.g., Figs. 3A, G View Fig ). The winding plane of this spire is arranged perpendicular to the plane of biseriality. The chambers are interconnected by basal (interiomarginal) slit-like foramina. The early planispiral stage is followed by a biserial stage that consists of up to 25 chambers also displaying interio-marginal foramina ( Fig. 3B View Fig ). The biserial chambers gradually increase in width while the height remains more or less constant. The relationship between the relevant parameters, number of chambers in the biserial stage and the total test height exhibits a linear curve regression ( Fig. 4 View Fig ). The chambers are subdivided by four to five vertical partitions (or beams) protruding into the lumen without reaching the center (= plane of biseriality). Horizontal partitions (one or two?) may be present in the last ontogenetic adult part of the test. Cross-sections through the adult test part display vertical partitions (usually four per chamber) ( Figs. 3 View Fig M-O, Q-S). The wall is homogeneous (noncanaliculate), microgranular to finely agglutinated.

Dimensions: See table 1.

Remarks: On the one hand, the available biometric data of the Iranian specimens lie within the known range of the original material as recorded by Magniez (1972) but extends this at both the lower and upper end (e.g., test length: Fig. 4 View Fig ). Axial sections, especially of juvenile specimens appear to be simple and undivided, and can therefore be confused with a variety of biserial agglutinated taxa that exhibit an initial planispiral stage such as, for example, representatives of the Spiroplectammininae Cushman, 1927 (e.g., Loeblich & Tappan, 1987).

Stratigraphy: In the Taft Formation of SW Iran, N. producta occurs in inner platform wackestones-packstones associated with other (larger) benthic foraminifera ( Fig. 2 View Fig ). Among the orbitolinids, the species may be associated with praeorbitolinids, mesorbitolinids, Iraqia simplex Henson, Palaeodictyconus actinostoma Arnaud-Vanneau & Schroeder and Dictyoconus? pachymarginalis Schroeder indicating an overall Aptian age. The type-material of Spain is latest Aptian-earliest Albian in age ( Magniez, 1972). Arnaud-Vanneau (1980) recorded N. producta from an interval spanning the early Barremian to the early Aptian of southern France and Kirmaci et al. (1996) from the late Aptian of Turkey. A late Aptian age was indicated also by Koch et al. (1998) for occurrences in Slovenia.

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