Discorbinasimulatilis Schwager, 1883:120, pl. 29: fig. 15a-d [? Zone P4, Farafra Oasis, Egypt],
Globorotaliaocclusa Loeblich and Tappan, 1957a: 191, pl. 55: fig. 3a-c [Zone P4, Vincentown Fm., New Jersey], pl. 64: fig. 3a-c [holotype, Zone P4, Velasco Shale, Tamaulipas, Mexico].—Luterbacher, 1964:690, text-figs. 112a-II 3c [Globorotaliavelascoensis Zone, Velasco Fm., Ebano, eastern Mexico], text-fig. 114a-c [Globorotaliavelacoensis Zone, Gubbio section, central Apennines, Italy].
Globorotaliacrosswicksensis Olsson, 1960:47, pl. 10: figs. 7-9 [Zone P3b, Hornerstown Fm., New Jersey],
Globorotalia (Truncorotalia) velascoensisocclusa Loeblich and Tappan.— Hillebrandt, 1962:139, pl. 13: figs. 22, 24, 25 [Zone F = Zone P4/5 this paper], pl. 13: figs. 23, 26 [Zone D = Globorotaliapusillapusilla Zone (upper part), Reichenhall-Salzburg Basin, Austro-German border].
Globorotalia (Morozovella) occlusa Loeblich and Tappan.—Jenkins, 1971:106, pl. 9: figs. 208-210 [Subbotina triloculinoides Zone, Waipawan Stage, Middle Waipara River section, New Zealand].—Blow, 1979:1007, pl. 90: figs. 7, 10 [lower part of Zone P4, DSDP Hole 21 A/3/6: 74-76 cm; South Atlantic Ocean], pl. 95: figs. 7-10, pl. 96: figs. 1-3 [Zone P5, sample FCRM. 1670, Lindi area, Tanzania], pl. 213: fig. 6. pl. 214: figs. 1-6, pl. 215: figs. 5, 6, pl. 103: figs. 4-6, pl. 108: figs. 9. 10 [Zone P6, lower part, DSDP Hole 20C/6/3: 76-78 cm; Brazil Basin. South Atlantic Ocean], pl. 118: figs. 1-7 [Zone P7, DSDP Hole 47.2/8/3: 83-85 cm; Shatsky Rise, northwestern Pacific Ocean].—Belford, 1984:9, pl. 17: figs. 6-14 [upper Paleocene, WABAG Sheet area, Papua, New Guinea].
Globorotalia (Morozovella) occlusacrosswickensis Olsson.—Blow, 1979:1011, pl. 88: figs. 1, 2, pl. 213: figs. 1,2 [upper part of Zone P3, DSDP Hole 47.2/10/1: 72-74 cm; Shatsky Rise, northwestern Pacific Ocean], pl. 90: figs. 3-6, 8, 9, pl. 213: figs. 3-5, pl. 215: figs. 1-4 [lower part of Zone P4, DSDP Hole 21 A/3/6: 74-76 cm; South Atlantic Ocean].
Morozovellasimulatilis (Schwager).—Snyder and Waters, 1985:470, pl. 9: figs. 7-9 [Zone P4/5, DSDP Site 549/16/4: 57-60 cm; northeastern Atlantic Ocean]. [Olsson et al. 1999]
Taxonomic discussion: The enhanced, expanded concept of M. occlusa applied by Hillebrandt (1962) to include biconvex forms with 5-8 chambers is followed herein (see also Gohrbandt, 1963; Luterbacher, 1964; Samanta, 1970). Blow (1979) interpreted this form as a morphologically and phylogenetically advanced (descendant) form of M. crosswicksensis Olsson, which was said to generally lack the circumumbilical muricate coronet present in M. occlusa. The former was described from Zone P3b (Hornerstown Fm., New Jersey); the latter was described from the Velasco Fm. (Zone P4) and is characteristic of Zones P4 and P5. We include crosswicksensis in the concept of the taxon occlusa; it bears a similar relationship to that observed in the Acarininacoalingensis! triplex (earlier rounded periphery)-/?ri »izriva (later angular periphery) morphotypic series. [Olsson et al. 1999]
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: Like M. acutispira but without raised early part of test.
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
Character matrix
test outline:
Lobate
chamber arrangement:
Trochospiral
edge view:
Equally biconvex
aperture:
Umbilical-extraumbilical
sp chamber shape:
Crescentic
coiling axis:
Moderate
periphery:
Muricocarinate
aperture border:
Thin lip
umb chbr shape:
Subtriangular
umbilicus:
Narrow
periph margin shape:
Subangular
accessory apertures:
None
spiral sutures:
Raised muricate
umb depth:
Deep
wall texture:
Smooth
shell porosity:
Finely Perforate: 1-2.5µm
umbilical or test sutures:
Moderately depressed
final-whorl chambers:
4-5
N.B. These characters are used for advanced search. N/A - not applicable
Biogeography and Palaeobiology
Geographic distributionThis species is widespread in the low to middle latitudes. [Olsson et al. 1999]
Aze et al. 2011 summary: Low to middle latitudes; based on Olsson et al. (1999) Isotope paleobiologyMorozovellaocclusa has δ13C and δ18O similar to coexisting M. velascoensis and Acarininamckannai and more positive δ13C and more negative δ18O than Subbotina spp. (Shackleton et al., 1985; Lu and Keller, 1996). [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); Lu & Keller (1996) Phylogenetic relationsThis species probably evolved from M. pasionenesis by a decrease in umbilical size, development of a biconvex test, and reduction of the muricate, sharp adumbilical ridges to lightly muricate, gently rounded surfaces around the umbilicus. Morozovellaocclusa is a sister species to M. acutispira, with which it shares the biconvex test shape and relatively constricted umbilicus. [Olsson et al. 1999]
Most likely ancestor:Morozovella pasionensis - at confidence level 4 (out of 5). Data source: Olsson et al. (1999) f5a.
Biostratigraphic distribution
Geological Range: Notes: Top of Zone P3b (typical crosswicksensis); Zone P4-P5 (typical occlusa). [Olsson et al. 1999] Last occurrence (top): at top of E2 zone (100% up, 55.2Ma, in Ypresian stage). Data source: Olsson et al. (1999) f5a First occurrence (base): near top of P3b subzone (90% up, 60.8Ma, in Selandian stage). Data source: Olsson et al. (1999) f5a
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. 62
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
Gohrbandt, K. (1963). Zur Gliederung des Palaeogen im Helvetikum nordlich Salzburg nach planktonischen Foraminiferen. Mitteilungen der Geologischen Gesellschaft in Wien. 56(1): 63-. 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
Loeblich, A. R. & Tappan, H. (1957b). Planktonic foraminifera of Paleocene and early Eocene Age from the Gulf and Atlantic coastal plains. 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: 173-198. 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
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
Samanta, B. K. (1970). Middle Eocene Planktonic Foraminifera from Lakhpat, Cutch, Western India. Micropaleontology. 16(2): 185-215. gs
Morozovella occlusa compiled by the pforams@mikrotax project teamviewed: 10-12-2024