Carnets Geol. 19 (2)  

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Outline:

[Introduction] [Studied sections]
[Material and depository] [Systematics]
[Concluding remarks] [Bibliographic references] and ... [Plates]


Uteria naghanensis n. sp. (Dasycladale)
from the Upper Maastrichtian of Iran

Koorosh Rashidi

Department of Geology, Yazd University, 89195-741 Tehran (Iran)

Felix Schlagintweit*

* Corresponding author
Lerchenauerstr. 167, 80935 Munich (Germany)

Published online in final form (pdf) on February 3, 2019
DOI 10.4267/2042/69755
[Editor: Bruno Granier; language editor: Stephen Eagar]

Click here to download the PDF version!

Abstract

A new dasycladalean alga is described as Uteria naghanensis n. sp. from the late Maastrichtian Tarbur Formation of the Zagros Zone, SW Iran. It is a small to medium-sized, rather well calcified species with small articles each bearing one fertile ampulla, alternating with close-set verticils of numerous sterile laterals. Another characteristic is its comparably wide main axis. The genus Uteria Michelin was so far only known from the Paleogene (Danian-Lutetian). The discovery of U. naghanensis n. sp. in inner platform wackestone of the Tarbur Fm. documents the origination of the genus already in the uppermost Cretaceous within an area belonging to the Arabian Plate.

Key-words

• green algae;
• larger benthic foraminifera;
• systematics;
• palaeobiogeography;
• Arabian Plate

Citation

Rashidi K. & Schlagintweit F. (2019).- Uteria naghanensis n. sp. (Dasycladale) from the Upper Maastrichtian of Iran.- Carnets Geol., Madrid, vol. 19, no. 2, p. 21-33.

Résumé

Uteria naghanensis n. sp. (Dasycladale) du Maastrichtien supérieur d'Iran.- Une algue dasycladale nouvelle, Uteria naghanensis n. sp., provenant du Maastrichtien supérieur de la Formation Tarbur du Zagros (sud-ouest de l'Iran) est décrite. Il s'agit d'une espèce de taille petite à moyenne, assez bien calcifiée, avec des petits éléments portant chacun une ampoule fertile, disposés en alternance avec des verticilles serrés consitués de nombreuses latérales stériles. Cette algue est aussi caractérisée par son axe principal assez large. Le genre Uteria Michelin n'était jusqu'à présent connu que dans le Paléogène (Danien-Lutétien). La découverte d'U. naghanensis n. sp. dans des boues bioclastiques de plate-forme interne de la Formation Tarbur atteste de l'apparition du genre dès la partie terminale du Crétacé dans une région rattachée à la Plaque Arabe.

Mots-clefs

• algues vertes ;
• grands foraminifères benthiques ;
• systématique ;
• paléobiogéographie ;
• plaque arabique


Introduction

The Upper Cretaceous Tarbur Formation, named after the village of Tarbur (Fars Province), and cropping out in the SW Zagros basin, represents a predominantly carbonate lithostratigraphic unit that contains rich microfauna and microflora associated with rudists (James & Wynd, 1965). It extends from the northwest to the southeast of the Zagros basin along the western edge of the imbricated Zagros zone, between the main Zagros fault and the Sabzposhan fault to the east (Alavi, 2004). The Tarbur Formation overlies and interfingers (towards the southwest) with the Gurpi Formation.

The microflora of the Tarbur Formation is rather poorly known and consists almost exclusively of calcareous green algae with a clear dominance of Dasycladales. Some taxa of dasycladalean algae were illustrated in a few recently published papers (Abyat et al., 2012, 2015; Afghah & Farhoudi, 2012; Afghah & Yaghmour, 2014; Afghah, 2016; Dehghani et al., 2016; Khosrow Tehrani & Afghah, 2004). These determinations however are dubious if not incorrect and therefore require further investigation. First results and critical revisions of the microflora of the Tarbur Formation were published recently (Rashidi et al., 2013; Schlagintweit et al., 2016c; Rashidi & Schlagintweit, 2018a, 2018b). The taxa identified so far include Clypeina sp. (rare), Dissocladella n. sp., Pseudocymopolia anadyomenea (Elliott) (common to abundant), Salpingoporella pasmanica Radoičić (common), Zittelina ? arumaensis (Okla) (rare to common), and Suppiluliumaella tarburensis Rashidi & Schlagintweit (common). Compared to the (larger) benthic foraminifera, the microflora is less diversified. In the present paper a new common to abundant dasycladale is described as Uteria naghanensis n. sp. The material comes from two sections of the Tarbur Formation.

Studied sections

The studied samples are from two sections of the Tarbur Formation (Fig. 1 ).

Fig. 1

Figure 1: Location of the Naghan and Mandegan sections (the background is an excerpt from Google Maps)

Fig. 1

Click on thumbnail to enlarge the image.

A) Naghan section

The studied area in the folded Zagros belt is located approximately 50 km south west of Naghan town near Gandomkar village and is here named the Naghan section. In this locality, the Tarbur Formation unconformably rests on the Gurpi Formation and is overlain by the Paleocene Sachun Formation. Lithologically, the Gurpi Formation consists of dark shales, grey calcareous shales containing planktonic foraminifera. The Sachun Formation consists of gypsum, red shales, anhydrite and some layer of carbonates.

The thickness of the Tarbur Formation at the Naghan section is about 274 m. It is composed of medium to thick–bedded grey limestone, shales and marls and can be subdivided into five units:

The total vertical distribution of Uteria naghanensis n. sp. is shown in Figure 3 , along with other dasycladales and some of the larger benthic foraminifera. The new species occurs in generally poorly diversified foraminiferal-algal wackestone (Fig. 2 ). It may be associated with small rudists, and dasycladales Pseudocymopolia anadyomenea (Elliott), and Salpingoporella pasmanica Radoičić. Among the benthic foraminifera small miliolids and rotaliids are typically co-occurring as well as large forms such as Dicyclina schlumbergeri Munier-Chalmas, Broeckinella arabica Henson, Persiella pseudolituus Schlagintweit & Rashidi, Spirolina ? farsiana Schlagintweit & Rashidi and more rarely Omphalocyclus macroporus Lamarck, and Neobalkhania bignoti Cherchi et al. (Fig. 3 ). The Greenwich coordinates of the section base are N 31°47'52" and E 50°32'53".

Fig. 2
Click on thumbnail to enlarge the image.

Figure 2: Microfacies with Uteria naghanensis n. sp. from the Naghan section. 1. Wackestone with small rudists. Thin-section 2NG 197. Scale bar 0.9 mm. 2. Wackestone with miliolids among Pseudonummoloculina kalantarii Schlagintweit & Rashidi. Thin-section N 83. Scale bar 0.6 mm.

B) Mandegan section

The study area, located in the High Zagros Belt, is situated north of Mount Dena, about 65 km south of the town of Semirom. The section of the Tarbur Formation is exposed about 10 km south of the village of Mandegan, and was named the Mandegan section (for further details of the location see Schlagintweit et al., 2016a). There the Tarbur Formation with a thickness of ~272 m conformably overlies the Gurpi Formation. The top of the section is unconformably overlain by conglomerates of the Pliocene Bakhtiari Formation. Based on the lithostratigraphy, the section has been subdivided into three units (from base to top): unit 1 is dominated by thick-bedded limestones, unit 2 mostly contains medium-bedded limestones with intercalated marly limestone layers, and unit 3 consists of marly limestone. The microfacies with Uteria naghanensis n. sp. is equivalent to the one from the Naghan section. The Greenwich coordinates of the Mandegan section base are N 31º25'8.13'' and E 51º24'34.58''.

Fig. 3
Click on thumbnail to enlarge the image.

Figure 3: Vertical distribution of selected dasycladaleans, including Uteria naghanensis n. sp. (green bar), and some larger benthic foraminifera in the Late Maastrichtian of the Tarbur Formation of the Naghan section.

Material and depository

All specimens from Uteria naghanensis n. sp. are from thin-sections stored at the Ardakan Payame Noor University, Iran, in the Rashidi collection, under the original sample numbers with the prefixes NG and 2NG for the Naghan, and Rt for the Mandegan sections. Twenty thin-sections from the Mandegan section have been stored at the Bayerische Staatssammlung für Paläontologie und historische Geology, Munich, under the official number SNSB-BSPG 2016 V 1 to V 20. They have been stored in the framework of the orbitolinid study of the authors (Schlagintweit et al., 2016b).

Systematics

Phylum Chlorophyta

Class Dasycladophyceae

Oder Dasycladales Pascher, 1931

Family Polyphysaceae (Kützing, 1843)

Tribe Uterieae (L. Morellet & J. Morellet, 1922), Bassoullet et al., 1979

Genus Uteria (Michelin, 1845), Dieni & Radoičić, 1985

Type-species: Uteria encrinella Michelin, 1845

Remarks: Based on which was previously known (e.g., Deloffre & Génot, 1982) the genus Uteria was emended by Dieni and Radoičić (1985) with respect to the order of laterals. The emendation was based on one longitudinal section of U. sarda Dieni et al. from the Paleocene of Sardinia, and one oblique section of U. cf. brochii L. Morellet & J. Morellet from the Paleocene of Slovenia. The sterile laterals display a more or less constant diameter, only in the distal part do they widen towards the thallus surface. For two verticils, a small central depression of the distal end is visibly covered by a thin layer of calcite (? remnant of the original algal skeleton). Therefore the terminal end of the laterals displays a (seemingly?) bifurcating aspect interpreted by Dieni and Radoičić (1985) as secondaries. For the section of the Slovenian specimen, tufts of tiny tertiary laterals at the end of the fertile vertical are illustrated. Neither from the type-species U. encrinella Michelin nor any other species have these higher order laterals been observed later in the literature. We may presume that their occurrence (interpretation?) was doubted by subsequent authors (e.g., Deloffre et al., 1989, p. 5 "si elles existent" ?). Also the short summarized diagnosis presented by Génot & Granier (2011) does not refer to the existence of higher order laterals: "Segmented thallus. Alternation along the stalk of whorls of slender sterile lateral segments and of very enlarged fertile segments bearing short secondary segments".

Uteria naghanensis n.sp.

(Pls. 1 - 2 - 3 )

Origin of the name: The species name refers to the type-locality situated near Naghan town.

Holotype: Longitudinal-oblique section illustrated in Pl. 1 , fig. 1, thin-section NG 60.

Type locality: Naghan section (Fig. 1 ).

Type level: Mud supported limestones (wackestone, packstone) with small and larger benthic foraminifera, dasycladales, and small rudists of the Tarbur Formation.

Diagnosis: Medium-sized, well and uniform calcified representative of Uteria displaying a rather wide axial cavity. The articulated thallus consists of regularly alternating sterile verticils and fertile verticils. The sterile verticils consist of numerous tubular and laterally attaching laterals. The fertile verticils contain each one swollen fertile ampulla bearing numerous short laterals at their distal surface.

Description: Thallus cylindrical, occasionally slightly bended, consisting up sparry calcite. The comparably (for the genus!) strong calcification comprises both main axis and laterals (Pl. 1 , fig. 1). Obviously due to the wackestone facies and/or strong calcification, long fragments composed of numerous articles are common (Pl. 1 , fig. 1). Smaller fragments often with 3 to 5 linked articles (Pl. 1 , fig. 7). The articulated thallus aspect is well discernible in longitudinal section and due to an insertion at the plane of the sterile laterals. The thallus consists of alternating fertile and sterile laterals arranged perpendicular to slightly inclined towards the main axis. Articles (between two successive sterile verticils) display a rectangular shape with a slightly convex outer side in axial sections (Pl. 1 , fig. 7; Pl. 3 , fig. 2). Each article consists of a layer with numerous primary fertile laterals. In vertical section these are subglobular often displaying a flattened distal side (Pl. 1 , fig. 5). Occasionally tapering "bulges" at the proximal parts of the fertile lateral are discernible (Pl. 1 , fig. 7, left side). They could correspond to neighboring pores. Each fertile lateral is connected to the main axis by means of a central tubular pore slightly widening to the former. These pores lie exactly in horizontal planes. At the distal surface numerous short secondaries arise that are slightly widening throughout most of their length. Towards the exterior surface they show a more marked widening. In shallow tangential section the secondaries form a close-set and alternating pattern (Pl. 3 , fig. 8). The sterile laterals are thin, tubular and display a distal widening (Pl. 2 , figs. 5-6). Secondary laterals arising from the distal ends have not been observed.

Dimensions: The main biometric parameters are compiled in Table 1 below.

no. sample L D d d/D w H l p fert. l'
1 NG 10 3.2 2.1 1.5 0.72 - 0.24 0.29 0.19 0.08
2 NG 49 - 3.6 2.6 0.73 - 0.48 0.48 0.27 -
3 NG 59 - 2.4 1.8 0.75 - - - - -
4 NG 60 4.7 2.4 1.5 0.64 - 0.31 0.36 - -
5 NG 83 - 2.6 1.68 0.65 - 0.31 0.42 0.22 -
6 NG 85 - 1.54 1.0 0.68 - - - - -
7 NG 85 - 1.2 0.74 0.62 72 - 0.21 - -
8 NG 85-1 - 2.7 1.6 0.59 - 0.36 0.55 0.26 0.12
9 NG 117 5.2 3.2 2.2 0.69 - 0.36 0.54 0.31 0.17
10 NG 117 - 3.1 2.2 0.71 124 - 0.5 - -
11 NG 121 - 2.2 1.7 0.77 - - 0.32 - -
12 NG 123 - 3.55 2.3 0.65 - - - - -
13 NG 117 - 3.1 2.2 0.71 124 - - - -
14 2NG 49 6.6 3.17 1.6 0.50 - 0.43 0.85 0.2 0.24
15 2NG 76 - 3.2 2.0 0.64 - 0.43 0.53 0.32 0.08
16 2NG 76 8.8 2.0 1.26 0.63 - 0.36 0.43 0.25 0.16
17 2NG 79 4.58 1.7 1.0 0.61 - 0.26 0.37 - 0.12
18 2NG 85-4 - 3.2 1.9 0.6 - 0.5 0.5 0.33 0.12
19 2NG 85-4 - 2.9 1.8 0.62 - - 0.5 - -
20 2NG 91 5.8 2.5 1.2 0.48 - 0.4 0.6 0.28 -
21 2NG 94 - 2.2 1.54 0.7 - 0.35 0.32 0.22 0.11
22 2NG 123 6.3 - - - - 0.32 - - -
23 2NG 197 - 2.3 1.44 0.63 - 0.44 0.43 0.26 -
24 Rt 67-2 - 2.8 1.9 0.68 - 0.48 0.57 0.42 0.14
25 Rt 86 9.7 2.3 1.3 0.56 - 0.3 0.47 - -
26 Rt 86 - 1.4 0.8 0.57 76 - 0.3 - -
27 Rt 86 5.6 2.4 1.6 0.67 - 0.31 0.42 0.24 0.15
28 Rt 89-3 - 2.4 1.6 0.66 - 0.28 0.39 - -
29 Rt 98-3 - 2.5 1.9 0.76 - 0.34 0.31 0.23 -
31 Rt 98-3 - 2.4 1.45 0.6 - 0.35 0.4 0.26 0.13
31 Rt 98-3 6.25 2.6 1.70 0.65 - 0.32 0.4 0.24 -
Range (max.) (9.7) 1.4-3.6 0.74–2.60 0.48–0.77 72-124 0.24–0.50 0.21–0.85 0.19–0.42 0.08-0.24
Mean - 2.5 1.6 0.65 - 0.33 0.42 0.25 0.135

Comparisons: The genus Uteria includes 7 species so far: type-species Uteria encrinella Michelin, 1845 (Ypresian-Bartonian of France), Uteria brocchii L. Morellet & J. Morellet, 1922 (?Ypresian of Belgium), Uteria merienda (Elliott, 1968), Radoičić, 1990 (Paleocene of Iraq), Uteria sarda Dieni et al., 1983 (Danian-Selandian of Sardinia, Italy), Uteria irregularis Dieni et al., 1985 (Danian-Selandian of Sardinia, Italy), Uteria medizzai Dieni et al., 1985 (Danian-Selandian of Sardinia, Italy), Uteria mexicana Deloffre et al., 1989 (upper Paleocene or lower Eocene of Mexico). The comparison table (Table 2 below) concludes that Uteria naghanensis n. sp. differs from the other species by its small articles (H), length of sterile laterals (~ wall thickness) (l), and just one fertile ampulla per article (g). The number of sterile laterals per vertical is in the range indicated for other species.

Dim. (mm)
U. naghanensis n. sp.
U. brochii
L. Morellet & J. Morellet
U. cf. brochii
(Dieni & Radoičić)
U. sarda
Dieni et al.
U. irregularis
Dieni et al.
U. medizzai
Dieni et al.
U. mexicana
Deloffre et al.
U. merienda
(Elliott)
U. encrinella
Michelin
D 1.4-3.6 1.5-2.5 2.00-2.56 3.92-5.04 2.48-3.68 2.08-2.24 1.25-2.37 Up to 2.5 0.9-3.0
d 0.74-2.60 0.7-1.0 0.88-1.28 1.92-2.40 1.30-1.76 1.28-1.76 0.81-1.31 Up to 1.0 0.28-0.80
d/D 0.48-0.77 0.40-0.46 0.44-0.50 0.47-0.48 0.47-0.52 0.69 0.55-0.64 - 0.24-0.36
H 0.24-0.5 0.8-1.2 0.75-1.28 0.88-1.66 0.96 0.48-0.80 0.68-1.87 - 0.44-1.2
l 0.21-0.86 - - - < 0.86 - 0.43-0.62 - -
w 72-124 40-50 ~40 100-120 < 70 40-50? 30-40? 50 or more 40-50
g 1 1-3 - 2-3 2 - 2 (3) - 6
pfert. 0.19-0.42 - - - - - - - -
Stratigr. Upper Maastr. Selandian Selandian? Danian-Thanetian Danian-Thanetian Danian-Thanetian Selandian-Ypresian Danian-Thanetian Ypresian-Lutetian

Stratigraphy: The occurrence of Canalispina iapygia Robles-Salcedo et al., 2018, in the samples NG 99-101 of the Naghan section is worth mentioning, as this taxon has its first appearance in the late Maastrichtian (according to Robles-Salcedo et al., 2018). This age assignment is also supported by some of the other larger benthic foraminifera, such as Neobalkhania bignoti. For the Mandegan section, the Upper Maastrichtian is evidenced with an association of orbitoids and Siderolites calcitrapoides, Canalispina iapygia Robles-Salcedo et al. in the lower part followed upwards by the dasycladalean-bearing strata (see Schlagintweit et al., 2016a, for further details).

Concluding remarks

Uteria represents a dasycladalean alga that was previously believed to be an exclusively Paleogene genus (Deloffre & Granier, 1992; Bucur, 1999, Table 10; Barattolo, 2002, Table 1). The Iranian finds from the late Maastrichtian of the Tarbur Formation show that the genus originated in the Late Cretaceous passing the K/Pg boundary. Another example includes Jodotella Morellet & Morellet (see Deloffre & Génot, 1982, Table 1) reported later from the Maastrichtian (Parente, 1997) and late Santonian (Schlagintweit, 2004). Analyzing the taxonomic inventories of Late Cretaceous and Paleogene dasycladaleans, especially at the K/Pg boundary, Barattolo (2002, p. 21) concluded that in the Maastrichtian the "environmentally restricted facies show a fundamental scarcity in the algal content if compared to similar, younger Paleocene facies. On the other hand, evidence of a moderately rich and diversified upper Maastrichtian microflora is recorded in open shelf/margin facies". The latter statement is referring essentially to the Ciolo Limestone of Southern Italy (e.g., Parente, 1997). The microflora observed from the Tarbur Formation represents an example of inner platform facies that can be considered not really impoverished but of moderate diversity (e.g., Clypeina sp., Dissocladella n. sp., Salpingoporella pasmanica, Zittelina ? arumaensis, Cymopolia eochoristosporica, Uteria naghanensis, and some other undescribed taxa). Unfortunately the Tarbur Formation obviously did not pass into the early Paleogene as some authors believe (see discussion in Schlagintweit et al., 2016a). This hinders providing further indicators on the effect of the K/Pg boundary event to dasycladaleans (Barattolo, 2002, for details).

Bibliographic references

Abyat A., Afghah M. & Feghhi A. (2012).- Stratigraphy and foraminiferal biozonation of Upper Cretaceous sediments in southwest Sepid Dasht, Lurestan, Iran.- Australian Journal of Basic and Applied Sciences, Montreal, vol. 6, no. 13, p. 18-26.

Abyat A., Afghah M. & Feghhi A. (2015).- Biostratigraphy and lithostratigraphy of Tarbur Formation (Upper Cretaceous) in southwest of Khorram Abad (southwest Iran).- Carbonates and Evaporites, Berlin, vol. 30, no. 1, p. 109-118.

Afghah M. (2016).- Biostratigraphy, facies analysis of Upper Cretaceous – Lower Paleocene strata in South Zagros Basin (southwestern Iran).- Journal of African Earth Sciences, vol. 119, p. 171-184.

Afghah M. & Farhoudi G. (2012).- Boundary between Upper Cretaceous and Lower Paleocene in the Zagros Mountain Ranges of southwestern Iran.- Acta Geologica Sinica, Xian, vol. 86, no. 2, p. 325-338.

Afghah M. & Yaghmour S. (2014).- Biostratigraphy study of Tarbur Formation (Upper Cretaceous) in Tang-E Kushk and east of Sarvestan (SW of Iran).- Journal of Earth Sciences, Berlin, vol. 25, no. 2, p. 263-274.

Alavi M. (2004).- Regional stratigraphy of the Zagros foldthrust belt of Iran and its proforeland evolution.- American Journal of Science, Los Gatos, vol. 304, p. 1-20.

Barattolo F. (2002).- Late Cretaceous–Paleogene Dasycladaleans and the K/T boundary problem. In: Bucur I.I. & Filipescu S. (eds.), Research advances in calcareous algae and microbial carbonates.- Proceedings 4th IFAA Regional Meeting, Cluj Napoca (29 August-5 September 2001), p. 17-40.

Bucur I.I. (1999).- Stratigraphic significance of some skeletal algae (Dasycladales, Caulerpales) of the Phanerozoic. In: Farinacci A. & Lord A.R. (eds.), Depositional Episodes and Bioevents. Palaeopelagos Special Publications, Rome, vol. 2, p. 53-104.

Dehghani M., Vaziri S.H. & Ahmadi V. (2016).- Lithostratigraphy and microbiostratigraphy of the Tarbur Formation in the Zangeneh section of interior Fars (Folded Zagros), south of Iran.- International Journal of Humanities and Cultural Studies, Gafsa, vol. 2, no. 4, p. 1872-1884.

Deloffre R. & Génot P. (1982).- Les Algues Dasycladales du Cénozoïque.- Bulletin des Centres de Recherches Exploration-Production elf-Aquitaine, Pau, Mémoire 4, 247 p.

Deloffre R., Fleury J.-J., Fourcade É. & Michaud F. (1989).- Dasycladales (Algues vertes) du Paléocène-Éocène inférieur du Mexique.- Revue de Micropaléontologie, Paris, vol. 32, no. 1, p. 3-15.

Deloffre R. & Granier B. (1992).- Inventaire des Algues Dasycladales fossiles. I° partie- Les Algues Dasycladales du Tertiaire.- Revue de Paléobiologie, Genève, vol. 11, no 2, p. 331-356.

Dieni I., Massari F. & Radoičić R. (1983).- New Palaeocene Dasyclads from the vicinity of Orosei (Sardinia).- Comptes Rendus des Séances de la Société Serbe de Géologie, Belgrade, 1982, p. 41-50.

Dieni I., Massari F. & Radoičić R. (1985).- Palaeocene Dasycladalean algae from Orosei (Eastern Sardinia).- Memorie di Scienze Geologiche, Padova, vol. 38, 77 p.

Dieni I. & Radoičić R. (1985).- Emendation of Uteria Michelin, 1845 (Dasycladaceae).- Bolletino della Societá Paleontologica Italiana, Modena, vol. 23, no. 2, p. 375-379.

Elliott G.F. (1968).- Permian to Palaeocene calcareous algae (Dasycladaceae) of the Middle East.- Bulletin of the British Museum Natural History (Geology), London, Supplement 4, 111 p.

Génot P. & Granier B. (2011).- Cenozoic Dasycladales. A photo-atlas of Thanetian, Ypresian and Bartonian species from the Paris Basin.- Carnets de Géologie, Madrid, Book 2011/01 (CG2011_SP01), 44 p.

James G.A. & Wynd J.G. (1965).- Stratigraphic nomenclature of Iranian Oil Consortium Agreement Area.- AAPG Bulletin, vol. 49, no. 12, p. 2218-2232.

Khosrow Tehrani Kh. & Afghah M. (2004).- Microbiostratigraphy and microfacies study of the Tarbur Formation in northeast and southeast of Shiraz.- Geosciences, Tehran, vol. 12, no. 53, p. 74-87.

Michelin H. (1840-1847).- Iconographie zoophytologique. Description par localités et terrains des Polypiers fossiles de France et pays environnants.- P. Bertrand, Paris, 348 p. URL: https://doi.org/10.5962/bhl.title.11504

Morellet L. & Morellet J. (1922).- Nouvelle contribution à l'étude des Dasycladacées tertiaires.- Mémoires de la Société géologique de France, Paris, t. XXV, fasc. 2, no. 58, 35 p.

Parente M. (1997).- Dasycladales from the Upper Maastrichtian of Salento Peninsula (Puglia, Southern Italy).- Facies, Erlangen, vol. 36, p. 91-122.

Radoičić R. (1990).- Paleogene Dasycladalean algae from the subsurface of the western Iraqi desert.- Bulletin de l'Académie Serbe des Sciences et des Arts, Classe des Sciences mathématiques et naturelles, Sciences naturelles, Beograd, no. 32, p. 91-103.

Rashidi K., Schlagintweit F., Parvizi T., Bamdad L. & Saberzadeh B. (2013).- Late Cretaceous (Maastrichtian) dasycladalean algae from the Naghan area (Zagros Mountains, SW Iran): preliminary results.- Berichte der Geologischen Bundesanstalt, Wien, vol. 99 (11th Workshop Alpine Geological Studies & 7th IFAA), p. 114-115.

Rashidi K. & Schlagintweit F. (2018a).- Cymopolia eochoristosporica Elliott, 1968 (green alga, Dasycladale) from the upper Maastrichtian of the Tarbur Formation (SW Iran).- Cretaceous Research, vol. 82, p. 99-103.

Rashidi K., Schlagintweit F. (2018b).- Zittelina ? arumaensis (Okla, 1995) nov. comb. and Suppiluliumaella tarburensis n. sp. (Dasycladales) from the Upper Maastrichtian of Iran.- Arabian Journal of Geosciences, vol. 11, Article 418.

Robles-Salcedo R., Vicedo V. & Caus E. (2018).- Latest Campanian and Maastrichtian Siderolitidae (larger benthic foraminifera) from the Pyrenees (S France and NE Spain).- Cretaceous Research, vol. 81, p. 64-85.

Robles-Salcedo R., Vicedo V., Parente M. & Caus E. (2019, in press).- Canalispina iapygia gen. et sp. nov.: the last Siderolitidae Finlay, 1939 (larger foraminifera) from the upper Maastrichtian (Upper Cretaceous) of southern Italy.- Cretaceous Research.

Schlagintweit F. (2004).- Calcareous green algae from the Santonian Hochmoos Formation of Gosau (Northern Calcareous Alps, Austria, Lower Gosau Subgroup).- Zitteliana, Munich, vol. A44, p. 97-103.

Schlagintweit F., Rashidi K. & Barani F. (2016a).- First record of Gyroconulina columellifera Schroeder & Darmoian, 1977 (larger benthic foraminifera) from the Maastrichtian Tarbur Formation of SW Iran (Zagros Fold-Thrust-Belt).- GeoPersia, Tehran, vol. 6, no. 2, p. 169-185.

Schlagintweit F., Rashidi K. & Babapidour M. (2016b).- Orbitolinid foraminifera from the Late Maastrichtian of the Tarbur Formation (Zagros Zone, SW Iran).- Acta Palaeontologica Romaniae, Cluj-Napoca, vol. 12, no. 2, p. 29-46.

Schlagintweit F., Rashidi K. & Kivani F. (2016c).- On the occurrence of Salpingoporella pasmanica Radoičić, 2002, (Dasycladales) from the Late Maastrichtian of the Zagros Zone, SW Iran.- Acta Palaeontologica Romaniae, Cluj-Napoca, vol. 12, no. 1, p. 33-42.


Plates

Plate 1: Uteria naghanensis n.sp.

Naghan (1-5), Mandegan (6-7) sections, upper Maastrichtian of Iran. Scale bars 1 mm, except 5 = 0.5 mm.

Fig. 1: Longitudinal-oblique section; holotype specimen. Thin-section NG 60.

Fig. 2: Longitudinal-oblique section. Thin-section 2NG 49.

Fig. 3: Tangential section. Thin-section 2NG 83.

Fig. 4: Oblique section. Thin-section 2NG 85.

Fig. 5: Fragmentary longitudinal section. Thin-section NG 82.

Fig. 6: Oblique section. Thin-section Rt 67.

Fig. 7: Longitudinal section of three segments. Note the bulges at the proximal part of the fertile lateral (arrows). Thin-section Rt 67-2.

Pl. 1
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Plate 2: Uteria naghanensis n.sp.

Naghan (1-4, 7-8), Mandegan (5-6) sections, upper Maastrichtian of Iran. Scale bars 1 mm.

Fig. 1: Oblique section. Thin-section 2NG 85.

Fig. 2: Longitudinal-oblique section. Thin-section NG 10.

Fig. 3: Oblique section. Thin-section 2NG 83.

Fig. 4: Longitudinal section cutting six segments. Thin-section NG 83.

Fig. 5: Slightly oblique transverse section through sterile verticil. Thin-section Rt 67.

Fig. 6: Slightly oblique transverse section through sterile verticil. Thin-section Rt 67-2n.

Fig. 7: Longitudinal oblique section. Thin-section 2NG 91.

Fig. 8: Oblique section (right), and transverse sections through through sterile verticils. Thin-section NG 117.

Pl. 2
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Plate 3: Uteria naghanensis n.sp.

Naghan (1, 5, 7), Mandegan (2-4, 6, 8) sections, upper Maastrichtian of Iran. Scale bars 1 mm.

Fig. 1: Two oblique sections. Thin-section 2NG 85.

Fig. 2: Oblique section. Thin-section Rt 67-3.

Fig. 3: Tangential-oblique section. Thin-section Rt 98.

Fig. 4: Longitudinal section cutting six segments cutting 19 segments. Thin-section Rt 86.

Fig. 5: Slightly oblique transverse section through sterile verticil. Thin-section 2NG 197.

Fig. 6: Tangential section cutting 7 segments. Thin-section Rt 98-3.

Fig. 7: Longitudinal section. Thin-section NG 85-1.

Fig. 8: Tangential section. Thin-section Rt 72.

Pl. 3
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