Daughter taxa (time control age-window is: 0-800Ma) | ||||
Dipsidripella liqianyui Like D. danvillensis but with more evolute test, less lobate axial periphery, more flattened spiral side, broader interiomarginal aperture, and without secondary accessory apertures. | ||||
Dipsidripella danvillensis Test low trochospire, small, moderately lobate, increasing moderately in size, 4-6 in final whorl; sutures radial and depressed; umbilicus narrow to broad and moderately deep; aperture high arch; a semicircular accessory aperture may occur on the spiral side. | ||||
Dipsidripella sp. Specimens which cannot be assigned to established species |
Jenkins (1971) erected the monotypic subgenus Globorotalia (Testacarinata) to accommodate the small, planoconvex, carinate species Globorotalia inconspicua Howe, and he regarded his subspecies Globorotalia (Turborotalia) inconspicua aculeata as the non-carinate, hispid ancestor of G. (T.) inconspicua. Liu and others (1998) transferred inconspicua and aculeata to the new benthic genus Praepararotalia because of gross similarities in their “globigerinid” morphology and similar biofacies distributions that indicated a benthic mode of life. However, significant differences in wall texture, roundness of the equatorial periphery and apertural morphology between aculeata (which is now considered a junior synonym of danvillensis Howe) and the other species that Liu and others (1998) included in Praepararotalia, warrant their separation at the genus level. The most appropriate genus available for danvillensis is Dipsidripella, which was defined by Brotea (1995) to accommodate her new species D. hodisensis Brotea. This latter species was described from uppermost Eocene-lowermost Oligocene sediments in northern Transylvania, but it too is here considered a junior synonym of danvillensis (see discussion below).
Abundance of D. danvillensis in shallow to marginal marine biofacies, its near absence from pelagic carbonate deposits, its monolamellar wall structure, and its more positive oxygen and much more negative carbon isotope values relative to co-occurring planktonic species (Fig. 16.3) suggest it may have lived in a benthic or merobenthic habitat. However, the overall test morphology (e.g., presence of globular chambers, an interiomarginal aperture, and evenly scattered, smooth to pustulose test surface ornamentation) is typical of planktonic foraminifera. Because of the uncertainty regarding its mode of life and phylogenetic origin, Dipsidripella is placed in the Problematica category.
[Huber et al. 2006]
Catalog entries: Dipsidripella
Distinguishing features:
Parent taxon (Globigerinitidae): Microperforate
This taxon: monolamellar wall covered with randomly scattered short, blunt to hispid pustules
Morphology:
Wall type:
Size:
Phylogenetic relations
[Huber et al. 2006]
Geological Range:
Notes: Huber and others (2006) suggested that Dipsidripella danvillensis was restricted to the Eocene whereas D. liqianyui survived into Oligocene Zone O1. Subsequent study has shown that both species persisted well into the early Oligocene [Pearson et al. 2018]
Last occurrence (top): at top of O2 zone (100% up, 30.3Ma, in Rupelian stage). Data source: Total of ranges of the species in this database
First occurrence (base): within E9 zone (43.23-43.85Ma, base in Lutetian stage). Data source: Total of ranges of species in this database
Plot of occurrence data:
Primary source for this page: Pearson et al. 2018 - Olig Atlas chap.16 p.432 (major update of Huber et al. 2006 - Eocene Atlas chap 16, p. 493)
Fleisher, R. L. (1974a). Cenozoic planktonic foraminifera and biostratigraphy, Arabian Sea, Deep Sea Drilling Project, Leg 23A. Initial Reports of the Deep Sea Drilling Project. 23: 1001-1072. gs O Huber, B. T., Olsson, R. K. & Pearson, P. N. (2006). Taxonomy, biostratigraphy, and phylogeny of Eocene microperforate planktonic foraminifera (Jenkinsina, Cassigerinelloita, Chiloguembelina, Streptochilus, Zeauvigerina, Tenuitella, and Cassigerinella) and Problematica (Dipsidripella). 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 16): 461-508. gs O Jenkins, D. G. (1966b). Planktonic foraminiferal zones and new taxa from the Danian to lower Miocene of New Zealand. New Zealand Journal of Geology and Geophysics. 8 [1965](6): 1088-1126. gs Jenkins, D. G. (1971). New Zealand Cenozoic Planktonic Foraminifera. New Zealand Geological Survey, Paleontological Bulletin. 42: 1-278. gs Liu, C., Olsson, R. K. & Huber, B. T. (1998). A benthic paleohabitat for Praepararotalia gen. nov. and Antarcticella Loeblich and Tappan. Journal of Foraminiferal Research. 28(1): 3-18. gs Pearson, P. N., Wade, B. S. & Huber, B. T. (2018c). Taxonomy, biostratigraphy, and phylogeny of Oligocene Globigerinitidae (Dipsidripella, Globigerinita, and Tenuitella). 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 16): 429-458. gs OReferences:
Dipsidripella compiled by the pforams@mikrotax project team viewed: 12-10-2024
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