Globorotaliamembranacea (Ehrenberg). —Subbotina, 1953:205, pl. 16: fig. 13a-c [Paleocene, Tarkhankut Peninsula, Crimea] [in part, not pl. 16: figs. 7a-12c]. [Not Planulinamembranacea Ehrenberg, 1854.]
Globorotaliapseudomenardii Bolli, 1957a:77, holotype: pl. 20: figs. 14-16; paratype: pl. 20:fig.17 [Globorotaliapseudomenardii Zone, Lizard Springs Fm., Trinidad].—Loeblich and Tappan, 1957a: 193, pl. 47:fig.4a-c [Zone P4, Salt Mountain Limestone, Alabama], pl. 49:fig.6a-c [lower Zone P4, Homerstown Fm., New Jersey], pl. 54: figs. 10a-13c [Zone P4, Vincentown Fm., New Jersey], pl. 59:fig.3a-c [Zone P4, Aquia Fm., Maryland], pl. 60: fig. 8a-c [Zone P4, Nanafalia Fm., Alabama], pl. 63: fig. la-c [Zone P4, Velasco Fm., Mexico] [in part, not pl. 45: fig. 10a-c].—Bolli and Cita, 1960:26, pl. 33: fig. 2a-c [Globorotaliapseudomenardii Zone, Paderno d'Adda section, northern Italy].
Globorotalia (Globorotalia) pseudomenardii Bolli.—Hillebrandt, 1962:126, pl. 12: figs. 5a-6b [upper Paleocene beds of Reichhall-Salzburg Basin, Austria].—Blow, 1979:892, pl. 89: figs. 1-5 [Zone P4, DSDP Hole 21A/3/5: 74-76 cm; Rio Grande Rise, South Atlantic Ocean], pl. 94: figs. 1-5 [Zone P4, Lindi area, Tanzania], pl. 108: figs. 4-7 [Zone P4, DSDP Hole 20C/6/3 76-78 cm; Brazil Basin, South Atlantic Ocean], pl. Ill: figs. 1-4, pl. 112 figs. 2, 3, 9, 10 [Zone P4, Moogli Mudstones, Papua] [in part, not pl. 105 figs. 3, 7-10],
Planorotalitespseudomenardii Bolli.—Nederbragt and Van Hinte, 1987:587, pl. 1: figs. 1-16 [Zone P4, DSDP Site 605/46/4,46/6,46/3, 52/2; New Jersey margin, western North Atlantic Ocean]. — Nocchi et al., 1991:269, pl. 1: figs. 7-9 [Zone P4, ODP Hole 698A/11R/CC; northeast Georgia Rise, South Atlantic Ocean]. [Olsson et al. 1999]
Variants: Taxonomic discussion: There is considerable variation in the shape of the equatorial periphery, which varies from fairly smooth to strongly lobulate, depending on the rate of size increase or decrease of the final few chambers in the ultimate whorl. [Olsson et al. 1999]
Distinguishing features: Parent taxon (Globanomalina): Very low trochospiral; 5-6 chambers in final whorl; chamber-shape variable. Aperture interiomarginal, umbilical-extraumbilical, arch with narrow lip. Wall smooth, normally perforate, pustules in some species. This taxon: Test spiroconvex with distinct keel & sharply-angled axial periphery. Umbilicus narrow. 5 (rarely 6) chambers in final whorl.
NB These concise distinguishing features statements are used in the tables of daughter-taxa to act as quick summaries of the differences between e.g. species of one genus. They are being edited as the site is developed and comments on them are especially welcome.
Description
Diagnostic characters: The distinct keel, the sharply-angled axial periphery, spiroconvex test, and narrow umbilicus are distinguishing features. The number of chambers in the ultimate whorl is consistently 5, but rarely a 6 chambered form is observed. [Olsson et al. 1999]
Character matrix
test outline:
Lobate
chamber arrangement:
Trochospiral
edge view:
Inequally biconvex
aperture:
Umbilical-extraumbilical
sp chamber shape:
Petaloid
coiling axis:
Very low
periphery:
Single keel
aperture border:
Thin lip
umb chbr shape:
Subtriangular
umbilicus:
Narrow
periph margin shape:
Subangular
accessory apertures:
None
spiral sutures:
Weakly depressed
umb depth:
Shallow
wall texture:
Smooth
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
Biogeography and Palaeobiology
Geographic distributionWidely reported in the low to middle latitudes (Figure 18). [Olsson et al. 1999]
Aze et al. 2011 summary: Low to middle latitudes; based on Olsson et al. (1999) Isotope paleobiologyGlobanomalinapseudomenardii has δ18O and δ13C similar to Parasubbotinavarianta and S. velascoensis. The species has distinctly more positive δ18O and more negative δ13C than Morozovella, Acarinina, and Igorina. [Olsson et al. 1999] Aze et al. 2011 ecogroup 3 - Open ocean thermocline. Based on light _13C and relatively heavy _18O. Sources cited by Aze et al. 2011 (appendix S3): Olsson et al. (1999) Phylogenetic relationsThere is general agreement among workers that G. pseudomenardii originated from G. ehrenbergi (= G. haunsbergensis Gohrbandt) by an increase in the test size and the development of a peripheral keel. The species becomes extinct at the top of Zone P4. [Olsson et al. 1999]
Most likely ancestor: Globanomalina ehrenbergi - at confidence level 4 (out of 5). Data source: Olsson et al. 1999, fig 5a.
Biostratigraphic distribution
Geological Range: Notes: Zone P4. [Olsson et al. 1999]
The FAD of Globanomalina pseudomenardii marks the base of zone P4a / top of P3b (Wade et al. 2011) Last occurrence (top): at top of P4 zone (100% up, 57.1Ma, in Thanetian stage). Data source: zonal marker (Wade et al. 2011) First occurrence (base): at base of P4 zone (0% up, 60.7Ma, in Selandian stage). Data source: zonal marker (Wade et al. 2011)
Plot of occurrence data:
Range-bar - range as quoted above, pink interval top occurs in, green interval base occurs in.
Triangles indicate an event for which a precise placement has been suggested
Histogram - Neptune occurrence data from DSDP and ODP proceedings. Pale shading <50 samples in time bin. Interpret with caution & read these notes
Primary source for this page: Olsson et al. 1999 - Atlas of Paleocene Planktonic Foraminifera, p. 45
References:
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
Ehrenberg, C. G. (1854). Mikrogeologie: Das Erden und Felsen schaffende Wirken des unsichtbar kleinen selbständigen Lebens auf der Erde. Leopold Voss, Leipzig. 1-374. gs
Hillebrandt, A. , von (1962). Das Paleozän und seine Foraminiferenfauna im Becken von Reichenhall und Salzburg. Abhandlungen Bayerischen Akademie der Wissenschaften. 108: 1-182. gs
Nederbragt, A. J. & van Hinte, J. E. (1987). Biometric Analysis of Planorotalites pseudomenardii (Upper Paleo- cene) at Deep Sea Drilling Site 605, Northwestern Atlantic. Initial Reports of the Deep Sea Drilling Project. 93: 577-592. gs
Nocchi, M., Amici, E. & Premoli Silva, I. (1991). Planktonic foraminiferal biostratigraphy and paleoenvironmental interpretation of Paleogene faunas from the subantarctic transect, Leg 114. Proceedings of the Ocean Drilling Program, Scientific Results. 114: 233-273. 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. gs
Postuma, J. A. (1971). Manual of planktonic foraminifera. Elsevier for Shell Group, The Hague. 1-406. gs
Subbotina, N. N. (1953). Foraminiferes fossiles d'URSS Globigerinidae, Globorotaliidae, Hantkeninidae. Bureau de Recherches Geologiques et Minieres. 2239: 1-144. gs
Wade, B. S., Pearson, P. N., Berggren, W. A. & Pälike, H. (2011). Review and revision of Cenozoic tropical planktonic foraminiferal biostratigraphy and calibration to the geomagnetic polarity and astronomical time scale. Earth-Science Reviews. 104: 111-142. gs
Globanomalina pseudomenardii compiled by the pforams@mikrotax project teamviewed: 13-2-2026