arrayname: original
We change the species name to its masculine form to accord with Article 31.2 of the ICZN (“a species-group name, if it is or ends in a Latin or latinized adjective or participle in the nominative singular, must agree in gender with the generic name with which it is at any time combined”). Thus Protentelloides primitiva becomes P. primitivus. Protentelloides primitivus has a similar wall texture to the proposed ancestor G. atlanticus. Pore density is much lower than in G. variabilis and G. stainforthi. Longer ranging than its descendant, it exhibits a wide range of morphological variability in both the number of final whorl chambers and the nature of coiling. The morphologies assigned to this morphospecies clearly shows overlap with P. dalhousiei. We choose to separate the two due to the slightly higher stratigraphic appearance of forms that consistently have near-planispirally coiled and an elaborate aperture system. There are no published occurrences of this taxon since its description in 1995. In our recent studies of Oligocene material we find it in ODP Site 667, which is near to DSDP Site 366, but not outside of the eastern equatorial Atlantic Ocean where these two sites lie. [Coxall & Spezzaferri 2018]
Catalog entries: Protentelloides primitiva
Type images:Distinguishing features:
Parent taxon (Protentelloides): Laterally compressed, often with bulla/bullate final chamber
This taxon: Large, laterally compressed, low trochospiral/pseudoplanispiral, 4-6 chambers in the final whorl, final chamber reduced and bulla-like, sutures depressed, straight to curved; aperture an elongated slit at the base of the bulla-like final chamber.
Large and distinctive, Protentelloides primitivus differs from Globorotaloides atlanticus n. sp., from which it evolved, by the more irregularly shaped and inflated chambers, the deeply depressed sutures, more lobate peripheral outline and the distinctly equatorial position of the terminal bulla-like chamber. It differs from Globorotaloides hexagonus (Natland) in possession of a bulla and the equatorial-umbilical aperture. It is distinguished from Protentelloides dalhousiei in the slightly more involute coiling, the transitional position of the primary aperture, which is umbilical to extraumbilical, and in lacking accessory apertures. It also typically has fewer chambers in the final whorl than P. dalhousiei. It differs from Protentella prolixa Lipps (1964) in the lower stratigraphic range, possession of a bulla-like final chamber and the coarse cancellate wall. The tendency towards elongation of the final chamber represents another example of evolutionary convergence on a digitate form. [Coxall & Spezzaferri 2018]
Diagnostic characters:
Morphology:
Wall type:
Character matrix
test outline: | Lobate | chamber arrangement: | Pseudoplanispiral | edge view: | Equally biconvex | aperture: | Extraumbilical-peripheral |
sp chamber shape: | Globular | coiling axis: | Very low | periphery: | N/A | aperture border: | Bulla |
umb chbr shape: | Globular | umbilicus: | Wide | periph margin shape: | Broadly rounded | accessory apertures: | Intralaminal |
spiral sutures: | Weakly depressed | umb depth: | Shallow | wall texture: | Cancellate | shell porosity: | Finely Perforate: 1-2.5µm |
umbilical or test sutures: | Weakly depressed | final-whorl chambers: | 4-6 | N.B. These characters are used for advanced search. N/A - not applicable |
Geographic distribution
Isotope paleobiology
Phylogenetic relations
Most likely ancestor: Globorotaloides atlanticus - at confidence level 3 (out of 5). Data source: Coxall & Spezzaferri 2018 f4.1.
Likely descendants: Protentelloides dalhousiei;
plot with descendants
Geological Range:
Notes: Zhang and Scott (1995) report a short range for Protentelloides primitivus (~1.3 myr range), restricted to upper Oligocene Zone O7 (upper P22) (Spezzaferri, 1994; Zhang and Scott, 1995). Our recent studies based on ODP Site 667 material suggest this range can be extended into the early Miocene (Zone M1) (Fig. 4.1). [Coxall & Spezzaferri 2018]
Last occurrence (top): in mid part of M1b subzone (50% up, 21.8Ma, in Aquitanian stage). Data source: Coxall & Spezzaferri 2018 f4.1
First occurrence (base): near base of O7 zone (10% up, 25Ma, in Chattian stage). Data source: Coxall & Spezzaferri 2018 f4.1
Plot of occurrence data:
Primary source for this page: Coxall & Spezzaferri 2018 - Olig Atlas chap.4 p.119
Coxall, H. K. & Spezzaferri, S. (2018). Taxonomy, biostratigraphy, and phylogeny of Oligocene Catapsydrax, Globorotaloides, and Protentelloides. In, Wade, B. S., Olsson, R. K., Pearson, P. N., Huber, B. T. & Berggren, W. A. (eds) Atlas of Oligocene Planktonic Foraminifera. Cushman Foundation for Foraminiferal Research, Special Publication . 46(Chap 4): 79-124. gs Lipps, J. H. (1964). Miocene planktonic foraminifera from Newport Bay, California. Tulane Studies in Geology and Paleontology. 2: 109-133. gs O Olsson, R. K., Pearson, P. N. & Huber, B. T. (2006c). Taxonomy, biostratigraphy, and phylogeny of Eocene Catapsydrax, Globorotaloides, Guembelitrioides, Paragloborotalia, Parasubbotina, and Pseudoglobigerinella n. gen. In, Pearson, P. N., Olsson, R. K., Hemleben, C., Huber, B. T. & Berggren, W. A. (eds) Atlas of Eocene Planktonic Foraminifera. Cushman Foundation for Foraminiferal Research, Special Publication . 41(Chap 5): 67-110. gs O Spezzaferri, S. (1994). Planktonic foraminiferal biostratigraphy and taxonomy of the Oligocene and lower Miocene in the oceanic record. An overview. Palaeontographia Italica. 81: 1-187. gs Zhang, J. & Scott, D. B. (1995). New planktonic foraminiferal genus and species from the upper Oligocene, DSDP Hole 366A, Leg 41. Micropaleontology. 41(1): 77-83. gsReferences:
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Protentelloides primitivus compiled by the pforams@mikrotax project team viewed: 21-4-2025
Short stable page link: https://mikrotax.org/pforams/index.php?id=104334 Go to Archive.is to create a permanent copy of this page - citation notes |
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