Cribrohantkenina inflata Howe 1928 from: Toumarkine, M.Luterbacher, H.P. (1985): Paleocene and Eocene Planktic Foraminifera. In: Plankton Stratigraphy p. 87-154 . |
Notice: This catalogue page may contain unedited data.
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Species Cribrohantkenina inflata Howe 1928 |
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Diagnosis / Definition: |
Pearson et al. (2006):
DESCRIPTION.
Type of wall: Smooth, normal perforate,
probably non-spinose; tubulospines imperforate, smooth
or with fine striations.
Test morphology: Planispiral, biumbilicate, 5-
6 chambers in the final whorl increasing rapidly in size
as added; chambers polygonal or spherical and laterally
inflated in the adult whorl, especially the final chamber;
peripheral outline lobate or angular; chambers of the
adult whorl extended into a hollow tubulospine; primary
aperture is an equatorial arch, low or tall and narrow,
bordered by an imperforate lip, supplemented on the
final 1-3 chambers by one or more (up to 16) additional
areal apertures on the chamber face set in a delicate
perforate apertural 'plate', each additional aperture
surrounded by an imperforate thickened rim; sutures
depressed and curved with deep restricted umbilici,
pustules sometimes present in the umbilical region;
tubulospines short and triangular, or long and slender,
ends tapering to a point, positioned at the anterior
chamber edge, spanning the suture between chambers,
arising sharply from the supporting chamber and
inclined forward in the direction of coiling at a low angle
almost tangential with respect to the periphery in the
final stages and contacting adjacent younger chambers
along their outer periphery; penultimate tubulospines
may be completely enveloped by globular younger
chambers.
Size: Maximum diameter excluding
tubulospines is 0.58 mm and including tubulospoines
0.75 mm (Howe, 1928). Generally large, 0.40-1.0 mm. |
Discussion / Comments: |
Toumarkine & Luterbacher (1985):
Cribrohantkenina inflata is readily recognized by its 4 to 6 inflated chambers each carrying a stout spine in the last whorl and by its peculiar accessory areal apertures. The primary aperture is trilobate as in Hantkenina whereas the accessory areal apertures are tuberculate holes.
Van Eijden & Smit (1991):
Remarks. C. inflata was observed in samples from Section 121-757B-14H by a shipboard scientist.
Pearson et al. (2006):
DISTINGUISHING FEATURES.-
Cribrohantkenina
inflata is distinguished from H. nanggulanensis and all
other hantkeninids by the presence of one of more areal
apertures in addition to the primary aperture in the final
adult chamber(s). Foms possessing a deeply crenulated
primary aperture but no isolated additional aperture (a
condition that probably represents the transition from
H. nanggulanensis) are excluded from the genus. This
taxon contains some of the largest individuals among
modem and fossil planktonic foraminifera, attaining
shell sizes in excess of 1.0 mm.
DISCUSSION.-
Several species with cribrate apertural
systems of varying complexity have been described, i.e.,
Hantkenina infata Howe, Hantkenina mccordi Howe
and Wallace, Hantkenina danvillensis Howe and
Wallace, Hantkenina (Cribrohantkenina) bermudezi Thalmann and Hantkenina lazzarii Pericoli. In our
research we examined large populations of
Cribrohantkenina in ODP Sites 865 and 1053 (Coxall,
2000) but were unable to distinguish any clear
stratigraphical or geographical trends in this character
other than the first cribrohantkeninids tend to have a
single additional areal aperture. Therefore, we refer all
Cribrohantkenina morphotypes to the earliest named
taxon, Hantkenina inflata Howe. Serial removal of the
chambers of C. inflata reveals that chambers formed
earlier in ontogeny possess simple Hantkenina-type
apertures, thus pre-adult C. inflata are indistinguishable
from co-occurring H. nanggulanensis and H.
alabamensis. This observation serves to unite the two
genera as members of a closely related clade.
The additional apertures of this taxon may be
circular, oval or keyhole-shaped and are usually
symmetrically arranged along the equatorial plane. It is
likely that they developed by invagination of the margins
of a typical Hantkenina-type aperture (Bermudez, 1937;
Bandy, 1949; Barnard, 1954; Banner and Blow, 1959;
Ramsay, 1962; Blow and Banner, 1962; Dieni and Proto
Decima, 1964). Specimens with apertures transitional
in morphology between Hantkenina and
Cribrohantkenina demonstrate that the evolution
involved several steps and processes: broadening of the
high-arched triradiate aperture (as seen in H.
nanggulanensis); crenulation and invagination of the imperforate margin; and restriction of the primary
aperture, creating isolated areal opening(s) in the
imperforate surround.
The precise stratigraphic range of
Cribrohantkenina in the uppermost Eocene is difficult
to establish in many sites because of common dissolution
events associated with the Eocene/Oligocene climatic
transition (e.g., Shackleton and Kennett, 1975; Zachos
and others, 1996). Rare complete specimens, or more
commonly fragments of the characteristic aperture
system, have been found ranging up to the Eocenel
Oligocene boundary at Torre Cardela, Fuente Caldera,
and Molino de Cobo, Spain; Massignano, Italy; Tanzania
(PNP, unpublished data); and ODP Site 707, Indian
Ocean (Martinez-Gallego and Molina, 1975; Molina,
1986; Molina and others, 1988; Coccioni, 1988; Nocchi
and others, 1988; Coxall, 2000) confirming that this
genus existed in parallel with Hantkenina until their
apparently simultaneous extinction at the boundary. Van
Eijden (1995, p. 240) figured an interesting specimen
with Cribrohantkenina-like areal apertures from Zone E12. This speclmen has the morphology of H.
compressa, and is relatively small and compressed in
comparison to the forms found in the upper Eocene. No
other occurrences of Cribrohantkenina have been
recorded below Zone E14, hence Van Eijden's specimen
is considered a probable teratoid Hantkenina.
An important feature of our Cribrohantkenina
taxonomy is the synonomy of Cribrohantkenina lazzarii
(Pericoli) with C. inflata. Cribrohantkenina lazzarii has
been commonly recorded from the uppermost Eocene
of Italy and Spain. It is described as differing from C.
infata in having a more polygonal peripheral outline,
more compact coiling (Pericoli, 1958) and a higher
stratigraphic range, extending above the last occurrence
of C. inflata to the Eocene/Oligocene boundary (Dieni
and Proto Decima, 1964; Coccioni, 1988; Gonzalvo and
Molina, 1992). The holotype of C. lazzarii has been
examined under SEM for the first time in this work.
Micrograph images revea~yhath e holotype is crushed
and very poorly preserved (PI. 8.3, Figs. 15-16),
hampering recognition of the cribrate aperture and
exaggerating the polygonal morphology. In our
investigations of uppermost Eocene assemblages
(including DSDP Site 522, ODP Sites 707, Tanzania,
Torre Cardela, and Massignano) we were unable to
stratigraphically or morphologically distinguish the C. lazzarii morphotype from C. inflata at any location.
Furthermore we have found inflated forms of the C.
inflata-type ranging up to the Eocene/Oligocene
boundary at Massignano, Tanzania and in the Spanish
sections. In agreement with Coccioni (1988) and
Gonzalvo and Molina (1992) we recognize that some
forms of Cribrohantkenina have more polygonal
chambers and an angular peripheral outline. However,
we observe that this feature is also characteristic of
earlier stages of ontogeny in all specimens of
Cribrohantkenina and that loss of the final globular chamber through breakage (which is common in upper Eocene foraminiferal assemblages from the Tethyan region) changes the overall aspect of the shell considerably by emphasizing the pre-adult polygonal
form.
PHYLOGENETIC RELATIONSHIPS.-
Cribrohantkenina
inflata evolved gradually from H. nanggulanensis
in the late Eocene by modification and
invagination of the primary aperture in the final growth
stages. As in Hantkenina, there is a tendency for specimens to become smaller and less inflated in the
latest Eocene (cf. the C. lazzarii concept).
STRATIGRAPHIC RANGE.-
Upper Eocene. Upper
Zone E1 4 to the Eocene/Oligocene boundary.
GEOGRAPHIC DISTRIBUTION.-
Worldwide, lowmid
latitudes. Common at ODP Site 1053, North
Atlantic, ODP Site 865, Central Pacific and coastal
Tanzania. Absent from the high northern and southern
hantkeninid localities such as the Labrador Sea and New
Zealand.
STABLE ISOTOPE PALEOBIOL0GY.-
This species
tends to yield low ň18O and high ň13C compared to other
CO-existing species analyzed (Poore and Matthews,
1984; Coxall and others, 2000) indicating a warm,
surface mixed layer habitat. There is no size related ň13C enrichment
trend. |
Systematics: |
1 Superregnum Eukaryota
Regnum Protoctista
Phylum Ciliophora
Subphylum Postciliodesmatophora
Ordo Globigerinida
Superfamilia Hantkeninacea
Superfamilia Nonionacea
Familia Hantkeninidae
Genus Cribrohantkenina
Species Cribrohantkenina inflata
15 Classis Foraminifera
Genus Cribrohantkenina
Species Cribrohantkenina inflata
32 Ordo Foraminiferida
Familia Hantkeninidae
Genus Cribrohantkenina
Species Cribrohantkenina inflata
35 Ordo Foraminiferida
Superfamilia Globigerinaceae
Familia Hantkeninidae
Genus Hantkenina
Species Cribrohantkenina inflata
Species Hantkenina alabamensis
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Synonym list: |
Toumarkine & Luterbacher (1985):
Van Eijden & Smit (1991):
Pearson et al. (2006):
1928 Hantkenina inflata Howe. - Howe : p.14 pl. 14; fig. 2 [lower
Oligocene, Old Fort St Stephens Bluff, Alabama, USA]
1932 Hantkenina mccordi Howe & Wallace. - Howe & Wallace : p.55 pl. 10; fig. 1a-b [Eocene, Jackson Fm., Danville Landing, Ouachita
River, Louisiana]
1934 Hantkenina danvillensis Howe & Wallace. - Howe & Wallace : p.37 pl. 5; fig. 14, 17 [Eocene, Jackson Fm., Danville Landing,
Ouachita River, Louisiana]
1937 Hantkenina (Sporohantkenina) brevispina Cushman. - Bermudez : p. 151-152 pl. 19; fig. 7-10 [upper Eocene, Globorotalia cerroazulensis Zone, Palmer Station
1640, Ramal Juan Criollo of Central Jatibonico, Camaguay Province, Cuba];
[Not Cushman, 1925]
1939 Hantkenina inflata Howe. - Rey : p.327 pl. XXII; fig. 18a-b [Bartonian and lower
Oligocene, Nummulitique du Rharb, Marocco]
1946 Cribrohantkenina mccordi Howe & Wallace. - Cushman : p.38 pl. 7; fig. 18-22 [Eocene, Jackson Fm., Danville
Landing, Ouachita River, Louisiana]
1957 Cribrohantkenina bermudezi Thalmann. - Bolli et al. : p.29 pl. 2; fig. 9-11 (hypotypes USNM
P4784a-c); [Eocene, Pachuta Fm., Cocoa Sands, Choctaw
County, Alabama]
1958 Hantkenina lazzarii Pericoli. - Pericoli : p.17 pl. 1; fig. 1-3 [upper
Eocene-lower Oligocene, Camp. Fl2, Nera Ponte Rotto,
Fossombrone, Italy]
1962 Cribrohantkenina danvillensis Howe & Wallace. - Blow & Banner : p.128 pl. 15, fig. 19(i-vii);
pl. 15, fig. g-h [middle part of the Globigerapsis semiinvoluta Zone
to the top of the C. danvillensis Zone, Lindi area,
Tanzania]
1962 Cribrohantkenina bermudezi Thalmann. - Ramsay : p.86 pl. 16; fig. 11 [middle Eocene, Kitunda Bluffs, Lindi, Tanzania, Samples
WA 1981]
1964 Cribrohantkenina lazzarii Pericoli. - Dieni & Proto Decima : p.576 pl. 45, fig. 25;
pl. 46, fig. 26-20 [upper Eocene, Castelnuovo, Euganean Hills, Italy]
1964 Cribrohantkenina thalmanni Brönnimann. - Dieni & Proto Decima : pl. 46; fig. 31-34 [upper Eocene,
Castelnuovo, Euganean Hills, Italy]; [Not Brönnimann,
1952]
1968 Cribrohantkenina inflata Howe. - Raju : p.291 pl. 1; fig. 6 [Turborotalia cerroazulensis Zone,
Karaikal, Cauvery Basin, India]
1969 Cribrohantkenina inflata Howe. - Samanta : p.337 pl. 1; fig. 11a-b [upper Eocene Globorotalia cerroazulensis Zone of Bolli,
upper Eocene, Kopili Fm., Garo Hills, Assam, India]
1975 Cribrohantkenina lazzarii Pericoli. - Martinez-Gallego & Molina : p.180 pl. 1; fig. 1a-b [upper Eocene C. inflata to C. lazzarii Zone, Torre
Cardela, Spain]
1979 Cribrohantkenina inflata Howe. - Blow : p.1171 pl. 52, fig. 1-3;
pl. 243, fig. 1-3 [late Eocene Zone P16,
Lindi, Tanzania]
1988 Cribrohantkenina inflata Howe. - Coccioni et al. : 87-88 pl. 2, fig. 9-12;
pl. 13, fig. 1-8 [upper Eocene, Massignano stratoptype section, Italy]
1988 Cribrohantkenina lazzarii Pericoli. - Coccioni : p.88 pl. 1; fig. 1-3 [upper Eocene Zone PIS-P17, Massignano, Marche-
Umbria Basin, Italy]
2006 Cribrohantkenina inflata Howe. - Pearson et al. : p.223 pl. 8.3; fig. 1-16 (Pl. 8.3, Figs. 1-2: new SEMs of the holotype of Hantkenina inflata Howe);
(PI. 8.3, Figs. 9-10: new SEMs of the holotype of Hantkenina danvillensis Howe and Wallace);
(P1. 8.3, Figs. 11-12: new SEM~of the holotype of Hantkenina mccordi Howe and W
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Stratigraphy - absolute ages: |
LAD: 34 ± 0 [Ma], Berggren et al. (1995)
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Specimen: |
Howe Collection - Louisiana State University Museum , Inventory number: LSU H 16
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References: |
Howe,H.V. (1928): An observation on the range of the genus Hantkenina . Journal of Paleontology Vol. 2 p. 13-14
Howe,H.V. and Wallace,W.E. (1932): Foraminifera of the Jackson Eocene at Danville Landing on the Ouachita, Catahoula Parish, Louisiana . Bull. Louisiana Dept. Conservation Geol. Vol. 2 p. 18-79
Howe,H.V. and Wallace,W.E. (1934): Apertural characteristics of the genus Hantkenina with description of a new species . J Vol. 8 p. 35-37
Bermudez,P.J. (1937): Nuevas especies de foraminiferos del Eoceno, de Cuba . Mem. Soc. Cubana Hist. Nat. Vol. 11 p. 137-150
Rey,M. (1939): Distribution stratigraphique des Hantkenina dans le Nummulitique du Rharb (Maroc) . Bulletin de la Société Géologique de France Vol. 5 p. 321-341
Thalmann,H.E. (1942): Foraminiferal genus Hantkenina and its subgenera . American Journal of Sciences Vol. 240 p. 809-823
Cushman,J.A. (1946): A rich foraminiferal fauna from the Cocoa sand of Alabama . Cushman Lab. Foram. Res. Spec. Publ. Vol. 16 p. 1-40
Brönnimann,P. (1950): The Genus Hantkenina Cushman in Trinidad and Barbados, B.W.I. . Journal of Paleontology Vol. 24 p. 397-420
Bolli,H.M.; Loeblich,A.R. and Tappan,H. (1957): The Planktonic foraminiferal families Hantkeninidae, Orbulinidae, Globorotaliidae, and Globotruncanidae . U.S. National Museum Bull. Vol. 215 p. 3-50
Pericoli,S. (1958): Sulla presenza del genere Hantkenina Cushman nella Scaglia dell' Urbinate . Bollettino della Societa dei Naturalisti in Napoli Vol. 157 p. 2-26
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