praeangulata in this work, however, for the reasons given below. The holotype and one of the paratypes (3514/7) of quadratoseptata are characterized by 5 chambers in the last whorl and slightly (but distinctly) curved sutures sloping to a rounded to subangular, lobulate, noncarinate periphery. In both specimens, the early whorls are obscured, the tests are poorly preserved (strongly recrystallized), and the last chamber for each is missing. Paratype 3514/8 has a quadrate test and flat early whorls, and the chambers of its last whorl slope toward a distinctly subangular periphery. The test of this paratype is homeomorphic with the Pliocene noncarinate Globorotalia crassaformis. The remaining paratype (3514/9) is distinctly different, as it comes from a different locality and stratigraphic level, and it is referable to Acarinina mckannai. The drawing of this specimen is misleading and gives the impression of a morozovellid. A further problem lies in the fact that the specimens coil in the opposite direction to what is shown in the illustrations. The negatives were apparently retouched and printed backwards.
The Russian authors compared their new species with Acarinina pentacamerata Morozova, 1961, and A. praecursoria Morozova, 1961. Although believing that quadratoseptata may indeed be a senior synonym of praeangulata by 15 years, the fact that the type material of quadratoseptata is very poorly preserved and has been virtually ignored in Soviet/Russian literature (it was not mentioned by Shutskaya, 1970a, 1970b, in her comprehensive review of Paleocene-lower Eocene planktonic foraminifera) leads us to retain the name praeangulata for this morphospecies. [Olsson et al. 1999]
Catalog entries: Globorotalia (Acarinina) praeangulata
Type images:Distinguishing features:
Parent taxon (Morozovella): Test typically plano-convex, chambers strongly anguloconical.
Wall strongly pustulose (muricate) on parts of spire and umbilicus. Most species with muricocarina.
This taxon: Planoconvex, moderately lobulate test with 5-6 tangentially elongate chambers in last last whorl; umbilical sutures straight to weakly curved, incised; spiral intercameral sutures incised, weakly muricate, strongly recurved; peripheral margin strongly muricate but not muricocarinate; umbilicus narrow, deep; aperture an interiomarginal, umbilical-extraumbilical slit (with distinct lip in well preserved specimens).
Diagnostic characters:
Character matrix
| test outline: | Lobate | chamber arrangement: | Trochospiral | edge view: | Planoconvex | aperture: | Umbilical-extraumbilical |
| sp chamber shape: | Crescentic | coiling axis: | Low | periphery: | Muricocarinate | aperture border: | Thin lip |
| umb chbr shape: | Subtriangular | umbilicus: | Narrow | periph margin shape: | Moderately rounded | accessory apertures: | None |
| spiral sutures: | Raised muricate | umb depth: | Deep | wall texture: | Moderately muricate | shell porosity: | Finely Perforate: 1-2.5µm |
| umbilical or test sutures: | Moderately depressed | final-whorl chambers: | 5-6 | N.B. These characters are used for advanced search. N/A - not applicable | |||
Geographic distribution
species has been identified suggests a low to middle latitude distribution. [Olsson et al. 1999]
Aze et al. 2011 summary: Low to middle latitudes; based on Olsson et al. (1999)
Isotope paleobiology
18 and more negative 8 0 values than Subbotina spp. (Shackleton etal., 1985). [Olsson et al. 1999]
Aze et al. 2011 ecogroup 1 - Open ocean mixed-layer tropical/subtropical, with symbionts. Based on very heavy _13C and relatively light _18O. Sources cited by Aze et al. 2011 (appendix S3): Shackleton et al. (1985)
Phylogenetic relations
Most likely ancestor: Praemurica uncinata - at confidence level 3 (out of 5). Data source: Olsson et al. (1999) f5a (following Blow 1979) - alternative interpretation given on fig 5b, origin from Globanomalina imitata, following Olsson & Hemleben (1996). See evolution comments above..
Likely descendants: Acarinina strabocella; Morozovella angulata;
plot with descendants
Geological Range:
Notes: Zone P2 to Zone P3a. [Olsson et al. 1999]
Last occurrence (top): at top of P3a subzone (100% up, 61.3Ma, in Selandian stage). Data source: Olsson et al. 1999
First occurrence (base): near base of P2 zone (10% up, 62.6Ma, in Danian stage). Data source: Olsson et al. 1999
Plot of occurrence data:
Primary source for this page: Olsson et al. 1999 - Atlas of Paleocene Planktonic Foraminifera, p. 64
Blow, W. H. (1979). The Cainozoic Globigerinida: A study of the morphology, taxonomy, evolutionary relationships and stratigraphical distribution of some Globigerinida (mainly Globigerinacea). E. J. Brill, Leiden. 2: 1-1413. gs Bolli, H. M. (1957d). The genera Globigerina and Globorotalia in the Paleocene-Lower Eocene Lizard Springs Formation of Trinidad. In, Loeblich, A. R. , Jr., Tappan, H., Beckmann, J. P., Bolli, H. M., Montanaro Gallitelli, E. & Troelsen, J. C. (eds) Studies in Foraminifera. U.S. National Museum Bulletin . 215: 61-82. gs Davidzon, R. & Morozova, V. G. (1964). Планктонные и бентосные известковые фораминиферы бухарских слоев (палеоцен) Тадхикской депрессиы [Planktonic and benthonic calcareous foraminifers of the Bukhara Beds (Paleocene) of the Tadzhik depression]. Paleontologicheskiy Zhurnal. (3): 23-29. gs Olsson, R. K. & Hemleben, C. (1996). Phylogeny of Normal Perforate Paleocene Planktonic Foraminifera based on Wall Texture. [Abstract.]. In, North American Paleontology Conference, Washington, D.C, Abstracts with Program,. 294-. gs Olsson, R. K., Hemleben, C., Berggren, W. A. & Huber, B. T. (1999). Atlas of Paleocene Planktonic Foraminifera. Smithsonian Institution Press, Washington, DC. (85): 1-252. gsReferences:

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Morozovella praeangulata compiled by the pforams@mikrotax project team viewed: 12-11-2025
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