Globigerinainconstans Subbotina, 1953:58, pl. 3: figs. 1, 2 [holotype,fig.1; both specimensfromzone of rotaliform globorotaliids, Elburgan Fm., Kuban River, northern Caucasus = middle part of Acarininainconstans Zone of Leonova and Alimarina, I960],—Berggren, 1965:291, text-fig. 9:3, 4 [Zone P2, Mexia Clay member. Wills Point Fm., Midway Group, Mexia, Texas].
Transitional form between Globorotaliapseudobulloides (Plummer) and Globorotaliauncinata Bolli.—Bolli, 1957a:74, pl. 17: figs. 16-18 [Globorotaliauncinata Zone, lower Lizard Springs Fm., Trinidad],
Globorotalia (Acarinina) inconstans (Subbotina).—Leonov and Alimarina, 1960, pl. 3: figs. 1-3, 5-8 [Globorotaliainconstans Subzone: figs. 1, 7, Podkhoomok River section; figs. 2-6, Khieu River; fig. 8, Urukh River, northern Caucasus].
Globigerinascabrosa Bermudez, 1961:1196, 1197, pl. 5: fig. 5 [Petromex Well, 200 m, La Palma 56, Panuco, Veracruz, Mexico],
Globorotaliainconstans (Subbotina).—Luterbacher, 1964:650: figs. 19-23 [figs. 19, 23, topotypes from zone of rotaliform globorotaliids, upper part of Elburgan Fm., Kuban River, northern Caucasus; figs. 20, 22, Globorotaliatrinidadensis Zone, Gubbio section, central Apennines, Italy].
Globigerinaarabica El-Naggar, 1966:157, 158, pl. 18: fig. 6 [holotype from Sample 30, Gebel Owaina, Globorotaliacompressa/ 'Globigerinadaubjergensis Zone, upper Danian, Nile Valley, Egypt],
Acarininainconstans inconstans (Subbotina). —Shutskaya, 1970b: 108, pl. 6: figs. 4, 5 [middle part Acarininainconstans Zone:fig.4, western Turkmenia, Malyi Balkhan;fig.5, Elburgan Fm., northern Caucasus].
Globorotalia (Turborotalia) inconstans (Subbotina).—Blow, 1979:1080, pl. 71: figs. 6, 7 [Zone Pl, DSDP Hole47.2/1/1: top], pl. 75:figs.4-7 [Zone Pl, Lindi area, Tanzania], pl. 76: figs. 3, 6, 7 [Zone P2, DSDP Hole 47.2/10/6: 69-71 cm],fig.10 [Zone P2, Hole 47.2/10/5: 70-72 cm], pl. 77:fig.1 [Zone P2, DSDP Hole 20C/6/4: 72-74 cm; Brazil Basin, South Atlantic Ocean], pl. 81: figs. 1, 2 [Zone P2, DSDP Hole 47.2/10/4: 83-85 cm; Shatsky Rise, northwestern Pacific Ocean], pl. 233: figs. 4, 5 [Zone Pl, Lindi area, Tanzania],
Morozovellainconstans (Subbotina).—Berggren, 1992:564, pl. 1: figs. 12, 13 [Subzone Pic, ODP Hole 747A/19H/CC: Kerguelen Plateau, southern Indian Ocean]. [Olsson et al. 1999]
Taxonomic discussion: The extensive synonymy above reflects our current understanding and interpretation of this taxon. A variety of morphotypes have been ascribed to inconstans -trinidadensis -praecursoria over the past 40 years and assigned to the genera Globigerina, Globorotalia, Acarinina, Subbotina, and Turborotalia. We include this form in the genus Praemurica following the demonstration by Olsson et al. (1992) of a phylogenetically distinct and homogenous lower Paleocene cancellate, nonspinose lineage. One of us (W AB) has examined the type specimens of inconstans, praecursoria, trinidadensis, and schachdagica and the synonymic listing above is based to a large extent on those studies. The wide range of variation ascribed herein to this morphospecies unifies forms sharing the characteristics of a cancellate, nonspinose test intermediate between the pseudoinconstans -taurica morphology and the typically anguloconical, nonkeeled uncinata morphology. [Olsson et al. 1999]
Distinguishing features: Parent taxon (Praemurica): Test very low trochospiral, usually 5-6, globular to oval chambers in last whorl, periphery lobulate; Wall non-spinose, weakly cancellate; This taxon: 5-7 chambered test; rapidly expanding final whorl; sutures radial; aperture an interiomarginal, umbilical-extraumbilical slit with distinct lipped rim.
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
Wall type:
Soldan et al 2014 f01-2d.JPG
Character matrix
test outline:
Lobate
chamber arrangement:
Trochospiral
edge view:
Inequally biconvex
aperture:
Umbilical-extraumbilical
sp chamber shape:
Inflated
coiling axis:
Low
periphery:
N/A
aperture border:
Thin lip
umb chbr shape:
Inflated
umbilicus:
Wide
periph margin shape:
Broadly rounded
accessory apertures:
None
spiral sutures:
Strongly depressed
umb depth:
Shallow
wall texture:
Smooth
shell porosity:
Finely Perforate: 1-2.5µm
umbilical or test sutures:
Strongly depressed
final-whorl chambers:
5-6
N.B. These characters are used for advanced search. N/A - not applicable
Biogeography and Palaeobiology
Geographic distributionA cosmopolitan species in northern and southern hemisphere sections (Figure 28). [Olsson et al. 1999]
Aze et al. 2011 summary: Cosmopolitan; based on Olsson et al. (1999) Isotope paleobiologyPraemuricainconstans has more positive δ13C and more negative δ18O than Subbotina and Globanomalina but has a similar isotopic signature to P. taurica (Boersma and Premoli Silva, 1983; Berggren and Norris, 1997). There is a pronounced increase in δ13C with increased size in P. inconstans (Kelley et al., 1996). [Olsson et al. 1999] Aze et al. 2011 ecogroup 2 - Open ocean mixed-layer tropical/subtropical, without symbionts. Based on _13C lighter than species with symbionts; also with relatively light _18O. Sources cited by Aze et al. 2011 (appendix S3): Berggren & Norris (1997); Boersma & Premoli Silva (1983) Phylogenetic relationsThis morphospecies evolved from Praemuricapseudoinconstans by the development of umbilical-conical chambers in morphologically advanced forms, development of incised umbilical sutures, and an increase in the number of chambers in the final whorl. [Olsson et al. 1999]
Geological Range: Notes: Zone Pic to lower Zone P3. [Olsson et al. 1999] Last occurrence (top): near base of P3a subzone (10% up, 62.2Ma, in Danian stage). Data source: Olsson et al. (1999), fig. 5a First occurrence (base): at base of P1c subzone (0% up, 63.9Ma, in Danian stage). Data source: Olsson et al. (1999), fig. 5a
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. 73
References:
Berggren, W. A. (1965). Some Problems of Paleocene-Lower Eocene Planktonic Foraminiferal Correlations. Micropaleontology. 11: 278-300. gs
Berggren, W. A. (1992). Paleogene planktonic foraminifer magnetobiostratigraphy of the southern Kerguelen Plateau (sites 747-749). Proceedings of the Ocean Drilling Program, Scientific Results. 120: 551-568. gs
Bermudez, P. J. (1961). Contribucion al estudio de las Globigerinidea de la region Caribe-Antillana (Paleoceno-Reciente). Editorial Sucre, Caracas. (3): 1119-1393. gs
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
Hillebrandt, A. , von (1962). Das Paleozän und seine Foraminiferenfauna im Becken von Reichenhall und Salzburg. Abhandlungen Bayerischen Akademie der Wissenschaften. 108: 1-182. gs
Khalilov, D. M. (1956). 0 pelagicheskoy faune foraminifer Paleogenovykh otlozheniy Azerbaydzhana [Pelagic Foraminifera of the Paleogene Deposits of the Azerbaizhan SSR]. Trudy Instituta Geologii, Akademiya Nauk Azerbaidzhanskoi SSR. 17: 234-255. gs
Leonov, G. P. & Alimarina, V. (1960). Stratigrafiya i planktonnye foraminifery "perekhodnykh" ot mela k paleogeny sloev tsentral'nogo Predkavkazya [Stratigraphy and Plantonic Foraminifera of the Cretaceous-Paleogene "Transition" Beds of the Central Part of the North Caucasus]. In Problema V: Granitsa melovoi i paleogenovoi sistem. Mezhdunarodnyi Geologicheskii Kongress, XXI Sessiya, Doklady Sovetskikh Geologov, Izdatelstvo Akademiya Nauk. 29-60. gs
Luterbacher, H. P. (1964). Studies in some Globorotalia from the Paleocene and Lower Eocene of the Central Apennines. Eclogae Geologicae Helvetiae. 57: 631-730. gsO
Morozova, V. G. (1957). On the Foraminiferal superfamily Globigerinidea, nov. and some of its representatives (in Russian). Doklady Akademii Nauk SSSR. 114(5): 1109-1112. 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
Shutskaya, E. K. (1970b). Stratigrafiya, foraminifery i paleogeografiya nizhnego paleogena Kryma, predkavkaz'ya i zapadnoi chadsti srednei azii [Stratigraphy, Foraminifera and Paleogeography of the Lower Paleogene in the Crimea, Precaucasus and the Western Part of Central Asia]. Trudy Vsesoyuznego Neftyanogo Nauchno-Issledovatel'skogo Geologo-Razvedochnogo Instituta (VNIGRI). 70(1): 256-. gs
Soldan, D. M., Petrizzo, M. R. & Silva, I. P. (2014). Pearsonites, a new Paleogene planktonic foraminiferal genus for the broedermanni lineage. Journal of Foraminiferal Research. 44: 17-27. gs
Stott, L. D. & Kennett, J. P. (1990). The Paleoceanographic and Paleoclimatic signature of the Cretaceous/Paleogene boundary in the Antarctic: Stable isotopic results from ODP Leg 113. Proceedings of the Ocean Drilling Program, Scientific Results. 113: 829-848. gs
Subbotina, N. N. (1953). Foraminiferes fossiles d'URSS Globigerinidae, Globorotaliidae, Hantkeninidae. Bureau de Recherches Geologiques et Minieres. 2239: 1-144. gs
Praemurica inconstans compiled by the pforams@mikrotax project teamviewed: 9-9-2024