Dictyoconella? minima Henson, 1948

Rashidi, Felix Schlagintweit Koorosh & Babadipour, Movlud, 2016, Orbitolinid Foraminifera From The Late Maastrichtian Of The Tarbur Formation (Zagros Zone, Sw Iran), Acta Palaeontologica Romaniae 12 (2), pp. 29-46 : 34

publication ID

https://doi.org/ 10.5281/zenodo.13190340

persistent identifier

https://treatment.plazi.org/id/F54F87FC-FFA8-FFAA-7DCE-19302AF15E54

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Felipe

scientific name

Dictyoconella? minima Henson, 1948
status

 

Dictyoconella? minima Henson, 1948 View in CoL

Figs. 3a–b View Fig pars, 5–6

*1948 Dictyoconella minima n. sp. – Henson, p. 25, pl. 11, fig. 3, 8-10.

2008 Dictyoconella minima Henson – Boudagher Fadel, pl. 5.7, figs. 1-3 (paratypes).

2016 Montseciella sp. – Afghah, fig. 5d (not indicated in the legend of the figure but in the text on page 175; Tarbur Formation of south Zagros Basin).

Description: Test medium conical (apical angles 50–90 degrees); both sides and cone base slightly convex. Some transverse sections display an oval outline ( Figs. 3b View Fig , 5j View Fig ).

The initial part is characterized by a small spire (?trochospiral,?planspiral) of few chambers and with acute margin; its axis is almost parallel to the test side wall ( Fig. 6e, g, l View Fig ). The embryo is poorly visible and its detailed structure unknown ( Fig. 6h–i View Fig ). The exoskeleton consists of horizontal (rafters) and radial vertical partitions (beams) subdividing the chamber margins. The beams are continuous from one chamber to the next ( Fig. 5c, 5e, 5n–m View Fig ). They extend to a marginal through marking the boundary to the central zone. Their distal ends slightly bend upwards in direction to the apex ( Fig. 5k View Fig ). There are 2 to 3 shorter intercalary beams intercalated between the beams ( Fig. 5b, 5o–p View Fig ). There are two rafters of inequal length per chamberlet in the marginal zone ( Fig. 5a View Fig ). Shallow-tangential sections display a pattern of subrounded alveolar compartments (subepidermal network) ( Fig. 5f View Fig ). The boundary between the marginal and central zones is marked by a marginal through, in close proximity to the marginal foramina ( Fig. 5g, 5j, 5p View Fig ). The latter with oblique axis ( Fig. 5k View Fig ) form a row of circular openings corresponding to the number of beams in transverse sections ( Fig. 5o View Fig ). Indistinct parts of the central zone are filled with opaque micritic masses (fused pillars and/or secondary deposits) masking the original structure ( Fig. 5a, 5h View Fig , middle part of the cone; Fig. 6b–e View Fig ). In other parts of the central zone vertical interseptal elements (pillars) alternating between successive chambers are discernible (see Fig. 5h View Fig , youngest chambers; Fig. 6k View Fig ). The non-marginal foramenal axes in the central zone maybe vertical (as the pillars) but also oblique.

Dimensions (in mm; data from Henson, 1948, between brackets):

Test diameter (D): 0.7–1.9 mm (0.7–1.8 mm)

Test height (H): 0.8–1.4 (1.0– 1.5 mm)

D/H: 0.8–1.35

Numbers of chambers per 1 mm axial length: 12–16, mostly 15–16 (15)

Remarks: Henson (1948, p. 25) noted that the test of D. minima is conical but slightly compressed, so that the base shows an elliptical outline. Elliptical (or oval) outline of the test base is rare in orbitolinids. It is reported from the early Albian Mesorbitolina ovalis throughout its ontogeny (see Görög and Arnaud-Vanneau, 1996), and the juvenile part of the late Albian Carinoconus casterasi (Bilotte, Canérot, Moullade & Peybernès) (see Schroeder, 1985). The acute margin of the initial spire of D.? minima however shows affinities to Carinoconus (see further remarks below) thus offering an explanation that only transverse sections of the juvenile test part might be ellipsoidal in outline.

Another typical feature of D.? minima are the dark, irregular distributed microgranular masses of fused pillars (and/or secondary deposits?) in the central zone. This was also observed by Henson (1948, p. 26), stating that interseptal structures are sporadic and poorly defined in the central part of the test. Among the Orbitolinidae , secondary deposits in the central zone are an extreme exception. An example is the genus Carinoconus Cherchi & Schroeder , with the type-species C. casterasi from the Late Albian of Spain (Bilotte, Canérot, Moullade & Peybernès) (Cherchi and Schroeder, 1983; Schroeder, 1985; Loeblich and Tappan, 1987). A second species has been described as Carinoconus iraqiensis by Bernaus and Masse (2006) from the Cenomanian of Iraq. Marginal foramina and main partitions (beams) arranged in vertical lines in subsequent chambers however are not reported from the genus Carinoconus . Without further details on the structure of the embryonic apparatus and the initial part in centered sections however a reliable attribution of Dictyoconella? minima to any known ( Carinoconus ?, or new?) orbitolinid genus is not possible for the moment being.

Henson (1948) reported D.? minima “most probably” from the late Cenomanian or Turonian of Qatar (Dukhan no. 2 and 3 wells; Wasia Group, see figs. 1-2 in Sugden and Standring, 1975). In addition, Henson (op. cit, p. 26) noted “a single specimen, possibly of this species” from the Maastrichtian of Iraq. For the Dukhan oil field of Qatar, Hewaidy and Al-Hitmi (1994) established a Late Cenomanian “ Dictyoconella minima total range Zone”. Curiously, Boudagher-Fadel (2008, chart 5.2) indicated the range of D.? minima as Late Cenomanian–Santonian.

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