Research paper
In the shadow of giants: Calcareous nannoplankton and smaller benthic foraminifera from an Eocene nummulitic accumulation (Transylvanian Basin, Romania)

https://doi.org/10.1016/j.marmicro.2021.101988Get rights and content

Highlights

  • Detailed micropaleontological study of a nummulitic accumulation

  • Multivariate data analyses were performed.

  • Abiotic factors are the main control on the distribution of the assemblages.

  • Paleoecological parameters reflect a preference for shallow water.

Abstract

Nummulitic accumulations are an important component of the Eocene sedimentary record in the Neotethyan realm. Their age, paleoenvironmental significance and depositional model are almost exclusively based on the interpretation of the larger benthic foraminiferal assemblages. We show here, however, that the high-resolution study of the other, often neglected, microfossils (calcareous nannoplankton and benthic foraminifera) is crucial to better constrain the diversity and paleoenvironmental gradient along the nummulitic accumulation(s). The studied micropaleontological assemblages, recovered from the large Eocene (Bartonian) nummulitic accumulation in the northwestern Transylvanian Basin (Romania), suggest an inner shelf depositional environment. A depth and nutrient gradient along the nummulitic accumulation from the south to the north could be recognized. In the southern part of the study area the environment was shallow and oligotrophic with Zygrablithus bijugatus, Blackites inflatus, Neococcolithes dubius, Ericsonia spp., larger sized reticulofenestrids and epiphytic foraminifera taxa (Pararotalia, Lobatula and Cibicides) on a sandy substrate. The progressive deepening toward the north led to an increase in clay content and more nutrient-rich marine waters in which calcareous nannoplankton (especially Reticulofenestra minuta), agglutinated foraminifera and calcareous infaunal foraminifera (Nonion, Protelphidium and Reusella) proliferated. The calcareous nannoplankton and smaller benthic foraminiferal assemblages confirm and further constrain the Bartonian age of the studied nummulitic accumulation, previously based on the larger benthic foraminiferal SBZ 17 zone.

Introduction

The Nummulites genus of larger benthic foraminifera is a diverse group of Paleogene Rotaliida that was especially widespread and abundant in the Eocene shallow water marine realm around the Neotethyan margin (Schaub, 1981). The build-up of calcareous Nummulites tests led to the formation of nummulitic accumulations (sometimes referred to as nummulitic banks), a peculiar sedimentary record without a modern counterpart (Racey, 2001). Because these accumulations are both interesting from a paleoecological point of view and may also be important hydrocarbon reservoirs, their paleoenvironmental interpretation is an important area of scientific research (Racey, 2001; Papazzoni and Seddighi, 2018). However, published studies have often reported contradictory results because they either use a purely paleontological approach focusing on the paleoecological interpretation based on Nummulites, or a sedimentological approach in which the nummulitic tests are treated as simple grains (see Mateu-Vicens et al., 2012; Briguglio et al., 2017 and references cited therein).

To shed light on the paleoenvironmental interpretation of nummulitic accumulations, we carried out a high-resolution study of the calcareous nannoplankton and smaller benthic foraminiferal content of the well exposed and extended Eocene nummulitic accumulation in the Transylvanian Basin, Romania. This is a classic example of a nummulitic accumulation, usually interpreted as a nummulitic bank (Papazzoni and Sirotti, 1995; Kövecsi et al., 2016; Papazzoni and Seddighi, 2018) which preserves mainly in situ, or rarely para-autochthonous assemblages (see Kövecsi et al., 2016; Pleș et al., 2020). The Nummulites which form the main part of the studied nummulitic accumulation, if transported, are transported as a bed load over a short distance (decimeters, rarely meters) because they imbricate rapidly (Briguglio et al., 2017. Furthermore, the monospecific or the “odd pairs”- type (Hohenegger et al., 1999) bi-specific assemblages, and the micrit or clay filling the spaces between the Nummulites are interpreted as clues for the autochthonous origin of the studied nummulitic accumulation (Briguglio et al., 2017; Pleș et al., 2020). Even so the depositional environment and the paleoecology of its fossil groups are still not well understood. Previous studies either focused on the paleoecological interpretation of Nummulites (Papazzoni, 2008; Kövecsi et al., 2016) or sedimentological analyses (Proust and Hosu, 1996) when interpreting this sedimentary record. As a result, few studies have focused on the calcareous nannoplankton assemblages identified within and/or below the nummulitic accumulation when constraining the age of this deposit, with no reference to the paleoecology of the fossil assemblages (Bombiţă et al., 1975; Popescu et al., 1978; Gheța, 1984; Rusu et al., 2004). The smaller benthic foraminifera associated with Nummulites have been almost completely neglected, except in one study (Bombiţă et al., 1975), while those occurring just below the nummulitic accumulation were studied on a purely taxonomic basis (Popescu et al., 1978; Rusu et al., 2004) with no reference to their biostratigraphy or paleoecology. This is curious, because it is well known that marine microfossils are sensitive to external factors (biotic and abiotic) and have a high preservation potential in the sedimentary record. They can therefore be good indicators of changes in the environmental and paleoenvironmental settings (Murray, 2006). A study of the microfossil assemblages i.e., of calcareous nannoplankton and smaller benthic foraminifera that lived in the “shadow” of the larger benthic foraminiferal communities may therefore offer a better view on the paleoenvironment of nummulitic accumulations and can further constrain the age and paleoecology of these fossil communities.

Thus, we carried out biostratigraphic framing by detailed comparison with other Eocene biozonations, determined the main taxa and assemblages using statistical analysis of the micropaleontological data, and interpreted the paleoenvironmental significance of the recovered assemblages based on the ecological preferences of their main taxa.

Section snippets

Geological setting

The Transylvanian Basin has a Late Cretaceous to Neogene sedimentary record, divided into four tectonostratigraphic megasequences by regional unconformities and/or their correlative conformity surfaces: a late Cretaceous synrift; a Paleogene sag; an early Miocene flexural; and a middle to late Miocene back-arc basin (Krézsek and Bally, 2006). The Paleogene sag megasequence consists mainly of Eocene–Oligocene siliciclastic and carbonate sediments deposited in three different areas of the sag

Materials and methods

The nummulitic accumulation was sampled at high resolution: 21 exposures grouped around nine locations in the GSA and MSA of the Transylvanian Basin (see Fig. 1, Appendix A, B and Table S1 in Bindiu-Haitonic et al., submitted). The Rona (Ro) outcrop is the only one where the underlying layer, a clay level, can be identified and sampled, whereas the various stacking patterns and sedimentary structures are dominant in the southern part of the basin (Fig. 2). Except for the clay samples, the

Assemblage composition and species richness

Forty-three calcareous nannoplankton taxa were identified in the studied samples (Appendix C), but some of the specimens could only be determined at the genus level due to their poor preservation. In general, the preservation of the calcareous nannoplankton specimens is poor to excellent, with the most well-preserved specimens recorded in the southern part of the nummulitic accumulation (MSA). The calcareous nannoplankton assemblages are dominated by the following taxa: Reticulofenestra umbilica

Calcareous nannoplankton

The calcareous nannoplankton assemblages from the studied areas lack the main Eocene marker species and therefore their assignment to standard biozones is difficult. This is exemplified by previous studies, which do not specify the exact location of the studied calcareous nannoplankton assemblages—that is, whether they were recovered from the nummulitic accumulation (= N. perforatus level) or below and/or above it.

Bombiţă et al. (1975) and Popescu et al. (1978) described the calcareous

Conclusions

The absence of calcareous nannoplankton marker species led us to adopt the regional biozonation scheme proposed for the Bartonian deposits of the Transylvanian Basin and to compare it with the standard biozonation schemes for this interval. Thus, we correlate the nummulitic accumulation with the regional Reticulofenestra bisecta Zone and standard NP17/CP14 Zones. Based on the calcareous nannoplankton, the identified Pararotalia subinermis Interval Zone, the age of the nummulitic accumulation is

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgments

This study represents a contribution to the PALNATB project supported by UEFISCDI grant PN-III-P1-1.1-TE-2016-0793. Ramona Bălc thanks the CNCSIS–UEFISCSU, project PN–III–P3–3.6–H2020–2016–0015 for financial support. The authors are grateful to Péter Ozsvárt and an anonymous reviewer for their useful suggestions that have improved our paper. Lucian Barbu Tudoran is thanked for his assistance with scanning electron microscopy images and Barabás Emese, Jakab Anna and Veciunca Alina for their help

References (153)

  • J. Hohenegger et al.

    Habitats of larger foraminifera on the upper reef slope of Sesoko Island, Okinawa, Japan

    Marine Micropaleontology

    (1999)
  • R. Imai et al.

    Evidence for eutrophication in the northwestern Pacific and eastern Indian oceans during the Miocene to Pleistocene based on the nannoplankton accumulation rate, Discoaster abundance, and coccolith size distribution of Reticulofenestra

    Mar. Micropaleontol.

    (2015)
  • A. Kahn et al.

    Provincialism associated with the Paleocene/Eocene thermal maximum: temporal constraint

    Mar. Micropaleontol.

    (2004)
  • K. Kaiho

    Global changes of Paleogene aerobic/anaerobic benthic foraminifera and deep-sea circulation

    Palaeogeogr. Palaeoclimatol. Palaeoecol.

    (1991)
  • K. Kaiho

    Effect of organic carbon flux and dissolved oxygen on the benthic foraminiferal oxygen index (BFOI)

    Mar. Micropaleontol.

    (1999)
  • K. Kaiho et al.

    End-Cenomanian benthic foraminiferal extinctions and oceanic dysoxic events in the northwestern Pacific Ocean

    Palaeogeogr. Palaeoclimatol. Palaeoecol.

    (1994)
  • A.L. Kalb et al.

    Nannoplankton origination events and environmental changes in the late Paleocene and early Eocene

    Mar. Micropaleontol.

    (2012)
  • S.A. Kövecsi et al.

    Odd partnerships among middle Eocene (Bartonian) Nummulites: examples from the Transylvanian (Romania) and Dorog (Hungary) basins

    Mar. Micropaleontol.

    (2016)
  • Cs Krézsek et al.

    The Transylvanian Basin (Romania) and its relation to the Carpathian fold and thrust belt: Insights in gravitational salt tectonics

    Mar. Pet. Geol.

    (2006)
  • A. McIntyre et al.

    Modern coccolithophoridae of the Atlantic Ocean – I. Placoliths and cyrtoliths

    Deep-Sea Research and Oceanographic Abstract

    (1967)
  • S. Monechi et al.

    Biotic signals from nannoflora across the iridium anomaly in the upper Eocene of the Massignano section: evidence from statistical analysis

    Mar. Micropaleontol.

    (2000)
  • Y.R. Narayan et al.

    Benthic foraminiferal assemblages from Moreton Bay, South-East Queensland, Australia: applications in monitoring water and substrate quality in subtropical estuarine environments

    Mar. Pollut. Bull.

    (2010)
  • Y.R. Narayan et al.

    Holocene benthic foraminferal assemblages indicate long-term marginality of reef habitats from Moreton bay, Australia

    Palaeogeogr. Palaeoclimatol. Palaeoecol.

    (2015)
  • J.G. Ogg et al.

    14 - Paleogene

  • H. Okada et al.

    Supplementary modification and introduction of code numbers to the low-latitude coccolith biostratigraphic zonation (Bukry, 1973;1975)

    Mar. Micropaleontol.

    (1980)
  • S. Ortiz et al.

    Palaeoenvironmental turnover across the Ypresian–Lutetian transition at the Agost section, Southeastern Spain: in search of a marker event to define the Stratotype for the base of the Lutetian Stage

    Mar. Micropaleontol.

    (2008)
  • C. Agnini et al.

    Responses of calcareous nannoplankton assemblages, mineralogy and geochemistry to the environmental perturbations across the Paleocene/Eocene boundary in the Venetian Pre-Alps

    Mar. Micropaleontol.

    (2006)
  • C. Agnini et al.

    Biozonation and biochronology of Paleogene calcareous nannoplanktons from low and middle latitudes

    Newsletter on Stratigraphy

    (2014)
  • M.P. Aubry

    Correlations biostratigraphiques entre les formations paleogenes epicontinentales de l’Europe du Nord-Ouest, basees sur la nannoplanton calcaire

    (1983)
  • M.P. Aubry

    Late Paleogene calcareous nannoplankton evolution: a tale of climatic deterioration

  • M.P. Aubry

    Early Paleogene Calcareous nannoplankton evolution: a tale of climatic amelioration

  • M.P. Aubry et al.

    Magnetic and calcareous-nannoplankton stratigraphy of the lower Paleogene formations of the Hampshire and London basins

    J. Geol. Soc.

    (1986)
  • F.T. Banner et al.

    Quaternary Haynesina n. gen. and Paleogene Protelphidium Haynes; their morphology affinities and distribution

    J. Foraminifer. Res.

    (1978)
  • J.M. Bernhard

    Characteristic assemblages and morphologies of benthic foraminifera from anoxic, organic rich deposits: Jurassic through Holocene

    J. Foraminifer. Res.

    (1986)
  • Bindiu-Haitonic, R., Bălc, R., Kövecsi, S.-A., Pleș, G., Silye, L., submitted. A dataset of calcareous nannoplankton...
  • A. Briguglio et al.

    Shear versus settling velocity of recent and fossil larger foraminifera: New insights on nummulite banks

    Palaios

    (2017)
  • G. Bombiţă et al.

    Éocène moyen-supérieur et Oligocène inférieur des environs de Cluj

  • P.R. Bown et al.

    Techniques

  • T.J. Bralower

    Evidence of surface water oligotrophy during the Paleocene–Eocene thermal maximum: nannoplankton assemblage data from Ocean Drilling Program Site 690, Maud Rise, Weddell Sea

    Paleoceanography

    (2002)
  • D. Bukry

    Low-latitude coccolith biostratigraphic zonation

    Initial Reports of the DSDP

    (1973)
  • R. Catanzariti et al.

    Late Eocene to Oligocene calcareous nannoplankton biostratigraphy in the northern Appennines: the Ranzano sandstone

    Memorie di Scienze Geologiche

    (1997)
  • D.F.R. Cleary et al.

    Relating species traits of foraminifera to environmental variables in the Spermonde Archipelago, Indonesia

    Mar. Ecol. Prog. Ser.

    (2007)
  • F. Cimerman et al.

    Late Eocene benthic foraminiferal fauna from clastic sequence of the Socka – Dobrna area and its chronostratigraphic importance (Slovenia)

    Geologija

    (2006)
  • S. Ćorić et al.

    Quantitative analyses of calcareous nannoplankton assemblages from the Baden-Sooss section (Middle Miocene of Vienna Basin, Austria)

    Geol. Carpath.

    (2008)
  • S. Ćorić et al.

    Roggendorf-1 borehole, a key section for Lower Badenian transgressions and the stratigraphic position of the Grund Formation

    Geol. Carpath.

    (2004)
  • B.H. Corliss et al.

    Morphotype patterns of Norwegian Sea deep-sea benthic foraminifera and ecological implications

    Geology

    (1988)
  • S. Dong et al.

    Responses of benthic foraminifera to changes of temperature and salinity: results from a laboratory culture experiment

    Science China Earth Sciences

    (2018)
  • D.L. Felder et al.

    Gulf of Mexico Origin, Waters and Biota

  • R. Fenero et al.

    Oligocene benthic foraminifera from the Fuente Caldera Section (Spain, Western Tethys): taxonomy and paleoenvironmental inferences

    J. Foraminifer. Res.

    (2012)
  • S. Filipescu

    Cenozoic lithostratigraphic units in Transylvania

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