Abstract
The new subfamily Redmondininae is characterized by coarsely perforated and strikingly thick chamber walls, a reduced umbilical filling but with a canal system that tends to extend onto the dorsal side of the shell. This group encompasses four genera (Redmondina, Slovenites n. gen., Rotaliconus, Pachyrotalia n. gen.). Seven species (R. henningtoni, R. garganica n. sp., S. praecursorius n. sp., S. pembaphis n. sp., S. decastroi n. sp., R. arachosiae n. sp., P. massa n. sp.), are described and illustrated.
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This is a group of rotaliids with coarsely perforated and strikingly thick chamber walls, a reduced umbilical filling but with a canal system that tends to extend onto the dorsal side of the shell. Few and coarse funnels may appear in the umbilical filling. Redmondina Hasson, 1985, represents a branch of small-sized shells with a relatively simple morphology, Slovenites n. gen. a parallel group with a more complex architecture and a peculiar dorsal ornamentation by perforate pustules. In Pakistan’s SBZ 4 (Upper Paleocene), they are associated to Pachyrotalia massa with an enveloping canal system invading the dorsal side.
All rotaliines and redmondinines remain limited in size during all the Paleogene; there are never extreme morphological variants like multiple spirals (Dictyoconoides, Dictyokathina) with their corresponding, extreme dimorphism.
1 Redmondina Hasson, 1985
Type species: Redmondina henningtoni Hasson, 1985
Remarks: The trochospiral shells with very coarse pores are comparatively small. The dorsal ornamentation is scarce and often obscured by the large pores. The periphery of the shell is rounded, without any differentiation of the perforation. The septa are radial, curved and inclined backwards on the dorsal side of the shell. They house a simple canal system with orifices near the junction of the spiral suture with chamber sutures. There seems to be a single radial canal in the septum below the septal suture (Plate 4.3, Fig. 2). The ventral side of the shell is characterized by radial, deeply sunk septa admitting a large, radial interlocular space. The foramina form very low and narrow arches in interiomarginal position (Plate 4.1, Fig. 13). The folia are long and narrow, only a little bit inclined in respect to the axis of the ventral part of the chambers. The narrow umbilicus is empty or filled with a few piles that do not fuse. The piles arise from the imperforate narrow folia along their radial axis (Plate 4.3, Fig. 2) but do not fuse to a solid umbilical filling. In early species, the umbilical plate is small and difficult to see in random sections of the shell. In later species, the umbilical plates are much larger. The spiral interlocular space is obscured by the heavy ornaments produced by the umbilical piles. We have not observed any dimorphic features.
Redmondina henningtoni Hasson, 1985; Plate 4.1, Figs 1–19; Plate 4.2, Figs. 1–13.
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1985 Redmondina henningtoni—Hasson, p. 352, pl. 3, figs. 4–9.
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? 1973 Epistomaria separans Le Calvez—Ferrer et al., p. 43, pl. 1, figs. 9–11.
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2000 Redmondina henningtoni (Hasson)—Peybernès et al., p. 46, pl. 6/7–8.
Remarks: A species with the characteristics of the genus Redmondina characterized by a smooth dorsal umbo covering the early whorls of the shell. The umbo has few or no pores forming a kind of white cap that strikes the eye when picking free specimens from washed residues. The adult whorls of the shell have 8–10 chambers. The size of the proloculus is about 0.04 mm. Compare the short, radial folia that do not touch each other with their adaxial tips in Hasson (1985, pl. 3, fig. 4) and in the present paper (Plate 4.1, Fig. 15).
Hasson’s (1985) holotype of R. henningtoni has a rounded periphery whereas her specimen illustrated pl. 3, fig. 4 shows a strong keel. I consider the latter as an artefact due to the glue used to prepare the specimen for SEM analysis.
Redmondina garganica n. sp.; Fig. 4.1A–J; Plate 4.3, Figs. 1–12.
Syntypes: Specimens figured in Plate 4.3, Fig. 3 (section perpendicular to coiling axis) and Fig. 9 (axial section).
Type locality and type level: Monte Gargano, Italy; Early Eocene, middle Cuisian (SBZ 11).
Derivation of name: Monte Gargano represents the highest point on the Peninsula Garganica, the spur of the Italian boot.
Diagnosis: Shells with the generic characteristics of Redmondina, somewhat larger than the type species. 12–14 inflated chambers are counted in the last adult whorl. The septal sutures are sunk without revealing the enlarged intraseptal interlocular space below that reaches from the ventral to the dorsal cameral suture with single orifices on both sides. The equatorial to axial diameter ratio for adult shells varies from 1.5 to 1.7.
Extending over the shell apex, the dorsal umbo is scarcely perforated but distinctly inflated. It may be composed of a certain number of dorsal piles grouped closely around the shell apex. Umbilical filling reduced to few, free umbilical piles standing on the foliar walls that fuse around the shell axis with one another without showing on the shell face any central plug. Proloculus diameter is about 0.04 mm.
Remarks: Redmondina garganica n. sp. is distinguished from R. henningtoni by the higher number of chambers in the last whorl, by a reduced size of the dorsal umbo and by a widening of the intraseptal interlocular space over the whole septum from ventral to dorsal.
2 Slovenites n. gen.
Type species: Slovenites pembaphis n. sp.
Diagnosis: The lenticular shells have a spiral chamber arrangement that is evolute on the dorsal side and involute on the ventral side. The lamellar chamber wall is particularly thick and perforated by very coarse pores. The folia are thick and perforate. They are inclined backwards and fused with their tips to the umbilical filling produced by previous whorls. This umbonal mass is composed of few, thick units separated by furrows in random directions (ilc in Fig. 1.2C). The foliar lumina are separated from the main chamber lumen by an umbilical plate similar to all Rotaliidae. Comparatively few funnels connect the interlocular space from the junction of the intraseptal with the spiral canals to orifices in the umbilical furrows or at the umbilical surface of the shell. The intraseptal space is reduced to a canal running closely above the rim of the foramen for the entire extension of the interiomargin of the septal face. It opens in an orifice positioned at the proximal junction of whorl and chamber sutures on the dorsal side of the test. The position of this orifice is illustrated in Fig. 1.2C (dsc: dorsal sutural canal orifice).
Remarks: Slovenites n. gen. is closest to Medocia Parvati, 1971 by its similar, coarse funnels. It differs from Medocia by its much coarser perforation, its ornamented dorsal side of the shell with sutural canal orifices, and by its fissures in the umbilical mass where part of the funnels open onto the substrate of the shell. Rotalia sensu stricto has no funnels in its umbilical filling, nor has it dorsal sutural orifices of the canal system. However, the foliar characteristics including the foliar apertures in Slovenites and Rotalia are so similar that we consider this new genus as a member of the Rotaliinae.
Slovenites is a conservative genus with a long range from Middle Paleocene (SBZ 2) to Lutetian (SBZ 13 at least). The earliest species, S. praecursorius, from SBZ 2 has been found in Sardinia. Slovenites pembaphis is widespread on the Adriatic platform in SBZ 4 and 5. Slovenites decastroi is present at several levels of the Monte Gargano Peninsula and of the Adriatic platform with alveolinids from SBZ 11–13.
Slovenites praecursorius n. sp.; Plate 4.4, Figs. 15–26.
Syntypes: Axial section figured in Plate 4.4, Fig. 15 and section almost perpendicular to the coiling axis figured in Plate 4.4, Fig. 25.
Type locality and type level: From sample F 4a, Sardinia, see Dieni et al. (1985); Paleocene (SBZ 2).
Derivation of name: precursor species of a genus discovered first in Slovenia.
Diagnosis: The shells are lenticular, equally convex on both sides, composed of three to four whorls of low-trochospiral chambers. The ratio equatorial to axial diameter oscillates between 1.3 and 2.0. The periphery is angular, lacking any keel and marked by a looser disposition of the pores. The cameral septa are curved backwards on their dorsal side, radial on their ventral side. They are flush on the dorsal side of the shell but marked by a deep interlocular fissure on the ventral side. An adult whorl has about 12 chambers. The folia have thick, perforate walls and fuse their proximal tips with the umbilical mass produced by previous whorls. At the junction of the intraseptal space with the umbilical interlocular space and in some places in the sutures of neighboring folia, wide open funnels are generated that seem to distribute their orifices at random over the ventral surface of the umbilical fill. The foramen is a very low, slit-like arch in interiomarginal position followed in ventral direction by a small, low umbilical plate.
Remarks: All known specimens of his taxon are from cemented carbonate rock. Their morphology can be defined only in thin sections. The minimum number of sections that permit to support a morphological definition of the taxon is two. These sections must be perpendicular to each other, one of them centered. Therefore, two syntypes are selected from the restricted material at our disposal.
Slovenites pembaphis n. sp.; Plate 4.5, Figs. 1–25; Plate 4.6, Figs. 1–2.
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1969 Lockhartia tipperi (Davies, 1926)—Butterlin and Monod, p. 586, pl. 1, fig. 7.
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1998 ?Kathina sp.—Accordi et al., p. 202, pl. 17, fig. 5.
Holotype: Megalospheric specimen figured in Plate 4.6, Fig. 1.
Type locality and type level: Sopada, Slovenia, Adriatic platforms, Paleocene (SBZ 3–SBZ 5).
Derivation of name: Slovenites, first discovery in Slovenia; pembaphis, Greek allusion to swelling walls and coarse pores like the state of a corpse floating for some time in the water.
Diagnosis: Lenticular shells composed of about four whorls of spiral chambers with thick, coarsely perforate walls. The lens is equally convex on both sides, reaching an equatorial diameter of 2.5 mm. The ratio of equatorial to axial diameter of the lens varies from 1.65 to 1.85. There are 10–12 slightly inflated chambers in an adult whorl. The umbilical architecture is described in the definition of the genus Slovenites above. The proloculus is small, reaching 0.08 mm in diameter. No dimorphism has been observed so far.
Slovenites decastroi n. sp.; Plate 4.6, Figs. 3–10; Plate 4.7, Figs. 1–12.
Holotype: Megalospheric specimen figured in Plate 4.6, Fig. 5.
Type locality and type level: Monte Gargano, Italy, samples A 4340, A 4344, collected by P. De Castro; Cuisian (SBZ 11–12) by association with alveolinids.
Derivation of name: in honour of Piero De Castro (Naples) and his work on the Monte Gargano.
Diagnosis: The lenticular shells are composed of five to six whorls of low-trochospiral chambers that are dorsally evolute and ventrally involute, with a wide umbilicus filled by thick foliar walls that are fused to a solid mass. The lens is almost equally convex (index 1.9–2.2); the ventral side however may be flatted in the center of the umbilicus. The lenticular shells reach an equatorial diameter of about 1.8 mm, with 20 dorsally isometric chambers in the adult last whorl. The megalosphere reaches a diameter of 0.12 mm at most. No dimorphism has been observed so far.
Remarks: Slovenites decastroi is distinguished from S. pembaphis by its larger number of spiral chambers that are arranged in a spiral with more whorls. The differences in the umbilical architecture all are due to the higher number of whorls and spiral chambers: the number of funnels increases with the number of septa in the adult whorls while the very first, small sized nepionic whorls do not develop any funnels and keep therefore the center of the umbilicus free of these structural elements.
3 Rotaliconus Hottinger, 2007
Type species: Rotaliconus persicus Hottinger, 2007
Rotaliconus arachosiae n. sp.; Fig. 4.2A–B; Plate 4.8, Figs. 1–11, 14–15.
Syntypes: Specimen figured in Plate 4.8, Figs. 1, 4. Rotaliconus arachosiae is known only from cemented rock of SBZ 4 (Late Paleocene) in Pakistan. Since there are only thin-sections available, syntypes have to be designated to fix the main diagnostic morphological elements.
Type locality and type level: All77232 and 77233, Zhob valley, Baluchistan, western Pakistan; Late Paleocene (SBZ 4), dated by association with “Orbitolina” daviesi Hofker jun., 1966.
Derivation of name: Arachosia, classical name of the country West of the Indus in times of Persian dominance (500 a. s.), corresponding today to the western Pakistani border provinces.
Diagnosis: High-conical shells with a subspherical outline produced by a rounded apex and a round periphery. The cone base is slightly flattened. The chamber walls are thick and coarsely perforate. In sections perpendicular to the wall surface, they seem to be ornate by numerous pustules, each carrying many pores. The “pustules” are intersections of the perforate shell between the enveloping canals covering the free chamber walls. The foramen seems to correspond to a very narrow slit (Plate 4.8, Fig. 1) in interiomarginal position placed on the dorsal angle of the septal face. The intraseptal interlocular space is widely open and undivided. The enveloping canals appear only below the surface of the chambers, whereas the interlocular space is bridged by numerous ponticuli. The folia are radial, short and loosely fuse at their tips to an umbilical mass that admits some funnels placed over the sutures of neighboring folia. Over the septal sutures of the main chambers the interlocular space is subdivided and transformed into a ventral enveloping canal system that is denser than on the dorsal side (Plate 4.8, Fig. 6).
The equatorial to axial diameter ratio is 1.0–1.5. There are 16–18 spiral chambers in the last whorl. The nepiont exhibits 9–10 chambers per whorl following a proloculus of 0.08 mm in diameter. No dimorphism of generations has been observed.
Remarks: Rotaliconus persicus Hottinger, 2007 from the late Lutetian-Bartonian of Iran has an outline of the shell and a habit of the umbilical architecture that is similar to the ones observed in Rotaliconus arachosiae from the Late Paleocene. R. persicus (Fig. 4.2C) is distinguished from R. arachosiae by the absence of a ventral canal system that envelops the main spiral chamber walls. There is only a single row of orifices for communication of the interlocular space in the septa with the ambient environment in front of the shell’s face.
4 Pachyrotalia n. gen.
Type species: Pachyrotalia massa n. sp.
Remarks: The test is coarsely perforated and has very thick walls. The trochospiral arrangement of the chambers throughout does not impede the subglobular shape of the shell.
Pachyrotalia massa n. sp.; Plate 4.8, Figs. 12–13; Plate 4.9, Figs. 1–15.
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1998 unidentified rotaliid—Accordi et al., p. 182, pl. 7, fig. c.
Syntypes: Specimens illustrated in Plate 4.9, Figs. 1–2 (top left), 4.
Type locality and type level: Sample All77232 collected by F. Allemann; Zhob valley, Baluchistan, western Pakistan; Paleocene (SBZ 4).
Derivation of name: Pachyrotalia for thick (walled) Rotalia, massa for heavy, massive umbilical plugs.
Diagnosis: Trochospiral shells with a subglobular outline (equatorial to axial diameter ratio is 1.1–1.3). The walls are very thick and perforate. The outer shell surface exposed to the ambient environment exhibits a loose meshwork of enveloping canals. Their radial parts interrupt the much finer, regular perforation of the walls. The periphery is rounded or slightly angular, always without any keeled marks. The narrow umbilicus is filed with a very massive, composed umbilical plug composed of several piles. Their separate origin is marked by funnels or fissures. The umbilical architecture is limited to a narrow space around the axial umbilical plug showing minute and thin folia covering a foliar chamberlet by small umbilical plates. The intraseptal interlocular space is comparatively wide and undivided, giving rise to the enveloping canal system on the abaxial, ventral as well as on the dorsal side of the shell. A single centered section (Plate 4.9, Fig. 4) reveals a megalosphere of 0.08 mm. At an early equatorial diameter of about 0.8 mm, the shell has 8 chambers per whorl.
References
Accordi G, Carbone F, Pignatti J (1998) Depositional history of a Paleogene ramp (Western Cephalonia, Ionian islands, Greece). Geol Romana 34:131–205
Butterlin J, Monod O (1969) Biostratigraphie (Paléocène à Eocène moyen) d’une coupe dans le Taurus de Beysehir (Turquie). Etude des Nummulites cordelées et révision de ce groupe. Eclogae geol Helv 62(2):583–604
Davies LM (1926) Remarks on Carter’s genus Conulites–Dictyoconoides Nuttall, with description of some new species from the Eocene of North West India. Rec Geol Surv India Calcutta 59(2):237–257, 16–20 pls
Dieni I, Massari F, Radoicic R (1985) Marine Paleocene pebbles included in the Cuccuru’e Flores Conglomerate (Post-Cuisian) of Orosei (Sardinia). In: 19th European micropaleontological colloquium excursion guide. AGIP Mineraria, San Donato Milanese, Milano, pp 213–214
Ferrer J, Le Calvez Y, Luterbacher H-P, Premoli-Silva I (1973) Contribution à l'étude des foraminifères Ilerdiens de la region de Tremp (Catalogne). Mém Mus Nat Hist Nat Paris, Sér C 29:3–107
Haque A (1958) Cincoriola, a new generic name for Punjabia Haque, 1956, Contr Cushman Lab Foram Res 9(4):103
Hasson PF (1985) New observations on the biostratigraphy of the Saudi Arabian Umm er Radhuma Formation (Paleogene) and its correlation with neighboring regions. Micropaleontology 31(4):335–364
Hottinger L (2007) Revision of the foraminiferal genus Globoreticulina Rahaghi, 1978 and of its associated fauna of larger foraminifera from the late Middle Eocene of Iran. Carnets Géol Article 2007/06, CG2007_A06
Parvati S (1971) A study of some rotaliid Foraminifera. Proc Kon Ned Akad Wetensch Ser B74(1):1–26, 4 pls
Peybernès B, Fondecave-Wallez M-J, Hottinger L, Eichène P, Segonzac G (2000) Limite Crétacé-Tertiaire et biozonation micropaléontologique du Danien-Sélandien dans le Béarn occidental et la Haute-Soule (Pyrénées Atlantiques). Geobios 33:35–48
Rahaghi A (1983) Stratigraphy and faunal assemblage of Paleocene-Lower Eocene in Iran. Nat Iranian Oil Comp Geol Lab 10, 73 pp, 49 pls
Robador A, Samsó JM, Serra-Kiel J, Tosquella J (1991) Field Guide. In: Introduction to the Early Paleogene of the south Pyrenean Basin. Early Paleogene Benthos 1st meeting IGCP nº 286, Jaca 1990, 131–159 pp
Sirel E (1998) Foraminiferal description and biostratigraphy of the Paleocene-Eocene shallow water limestones and discussion of the Cretaceous-Tertiary boundary in Turkey. Gen Dir Min Res Expl (MTA), Monograph ser 2, 117 pp, 68 pls
Smout AH (1954) Lower Tertiary foraminifera of the Qatar peninsula. Brit Mus (Nat Hist), 96 pp, 44 figs, 15 pls
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Bassi, D. (2014). New Subfamily Redmondininae. In: Bassi, D. (eds) Paleogene larger rotaliid foraminifera from the western and central Neotethys. Springer, Cham. https://doi.org/10.1007/978-3-319-02853-8_4
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