|
|
|
Annual Report 2011 of the Working Group on Paleogene Larger Foraminifera.
Unfortunately, the chairman Lukas Hottinger died recently, he could not send the report and we are looking for a new chairman.
Annual Report 2009-2010 of the Working Group on Paleogene Larger Foraminifera.
I have been discharged two years ago from the responsibility of leading the working group of larger foraminifera. Therefore I can give you only my personal contributions of the matter at hand. My state of health does not permit me to do fieldwork anymore but there are many corpses in the cellar awaiting a decent burial. Thus, I have finished and published a monograph on the Miscellaneidae and am working now on a revision of the larger Tethyan Paleogene Rotaliidae, mainly from Pakistan and Oman. This paper is scheduled to go to print in the same place in spring next year. Publications on paper take more and more time and increasing amounts of funding to be published. I have no more energy and time to wait. At request of the Museum Basel I just finished a bibliographic list of 2009:
Hottinger, L. (2009). The Paleocene and Earliest Eocene foraminiferal family Miscellaneidae: neither nummulitids nor rotaliids. Carnets de Géologie, article 2009/06, PDF p. 1-41.
Bassi, D., Hottinger, L. & Iryu, Y. (2009). Reassessment of "Boueina" pacifica Ishijima 1978 (Orbitolininae, Foraminiferida). Formerly considered as a green halimedacean alga. Journal Foraminiferal Research. 39 (2), 120-125.
Hottinger, L. & Caus, E. (2009). Meandropsinidae, an ophtalmidid family of Late Cretaceous K-stragegist foraminifera endemic in the Pyrenean Gulf. Neues Jahrbuch Geologie Paläontologie, Abhandlungen, vol. 253, no. 2-3, p. 249-279.
Boix, C., Vilalonga, R., Caus, E. & Hottinger, L. (2009). Late Cretaceous rotaliids (Foraminiferida) from the Western Tethys. Neues Jahrbuch Geologie Paläontologie, Abhandlungen. 253, 197-227.
Vicedo, V,. Aguilar, M., Caus, E. & Hottinger, L. (2009). Fusiform and laterally compressed alveolinaceans (Foraminiferida) from both sides of the Late Cretaceous Atlantic. Neues Jahrbuch Geologie Paläontologie, Abhandlungen. 253 (2-3), 229-247.
Report by Lukas Hottinger, Chairman of the Larger Foraminifera
Working Group.
Working Group on Paleogene
Larger Foraminifera – Report 2006 & 2007
Larger foraminifera are of increasing importance for dating shallow
water carbonate deposits where sequence stratigraphy and geochemical
stratigraphy meet with increasing problems and where planktonic
organisms are absent. In addition, the complex morphology of the
larger foraminifera that registers ontogeny, their abundance in
the sediment and their response to environmental requirements
provide new or more detailed insight into the mechanisms of community
maturation and evolutionary processes. The Paleogene epoch starting
after the K-T boundary event from scrap documents the maturation
of the benthic communities much better than the Late Cretaceous
cycles before and the Neogene cycles after this epoch that is
characterized by a long duration of climatic and biological stability.
In a period in which biology searches, beyond molecular mechanisms,
for new approaches to more complex systems and returns to organismic
biology, the historical dimension of life on Earth as recorded
by fossils is fundamental.
We are happy to announce, after several years, substantial progress
in the following fields:
1. Biozonation: G. LESS and coauthors have extended the Shallow
Benthic Zonation based on biometry to the nummulitic genera Heterostegina
(1) and Spiroclypeus (2) that confirm a revised zonation of orthophragminids
troughout the Eocene (3, 4) and the one of the nummulitids of
the Middle and Late Eocene and permit to subdivide these zones
into subzones.
2. Contributions to the knowledge on regional faunas, their composition,
ecology and age: With the work of E. SIREL (5) and the intensive
activity of E. ÖZCAN (6), the focus of interest is directed
to the immense potential of research in Turkey where the Paleogene
lithology, the ecological variation and the relative completeness
of the fossil record offer possibilities that are at least equivalent
to the ones in the Pyrenees (7). The Turkish faunas will provide
a key to the Middle Eastern hotspot (8) of diversity in Late Middle
Eocene to Oligocene times that characterizes the so-called Lockhartia
Sea. The full diversity will be recognized when the current studies
on the SaltRange in Pakistan by A. BUTT and co-workers (9, 10),
on Oman and on Sokotra by J. SERRA-KIEL and co-workers will be
completed.
On the Adriatic carbonate platform the Paleogene succession starts
early in SBZ 1 that contains an elphidiid index used for years
but formally described only now: Bangiana hanseni (11) with its
associated and subsequent Paleocene faunas (12). In the Carpathians
M. TISCHLER (13) has found Late Middle Eocene porcelaneous faunas
that clearly belong to a "Mediterranean" faunal province
with Borelis vonderschmitti whereas the Apulian platform (14)
was immerged by the Lockhartia Sea with Neorhipidionina. The Trentinara
formation characterizing the Lower to Middle Eocene deposits on
the Eastern side of the Apulian platform has produced Alveolinids
(15), a particular Periloculina (16), conical agglutinated (17)
and rotaliid foraminifera with a considerable number of new taxa
that are found also in Iran and Pakistan. In Spain, investigations
of the Paleocene faunas from the Betic realm are in progress.
3. Facies analysis of Priabonian shallow-water carbonate successions
in the outcrops near Mossano (eastern Colli Berici, north-eastern
Italy) and on Mt. Klokova (Greece) have been used to produce detailed
palaeoenvironmental models. The facies distribution and the processes
which controlled the larger benthic foraminiferal and coralline
algal assemblages are discussed in detail in terms of palaeoecology
and benthic community structure (18-20).
The term "Facies Dynamics" is introduced. This concept
aims to define and interpret spatial and temporal changes of carbonate
facies patterns. It is based on Middle Eocene to Early Oligocene
shallow-water carbonate facies types from the circumalpine area
(north-eastern Italy, northern Slovenia, Austria and southern
Bavaria), which are compared with respect to dominating biogenic
components and their distribution along the depth gradient on
the shelves (21).
4. The marginal basins around the core of the Tethys are of particular
interest for a better understanding of the response of larger
foraminifera to different kinds of stress. Intensive studies by
ZAKREVSKAYA and coworkers have updated and detailed the taxonomy
of nummulites and orthophragminids from the North-Eastern Peritethys
and assessed their biostratigraphic ranges. New endemic or facies-dependant
particular species are described (22), their age correlated with
cosmopolitan species to the SBZ zonation and where ever possible
with planktonic organisms (23-26). ZAKREVSKAYA's studies cover
an immense surface reaching from the Crimea and the Northern Caucasus
to Mangyschlak and the Northern Peri-Aralian (27). They demonstrate
the decrease of the diversity of the larger foraminifera with
time and with the increasing distance from the Tethyan oceanic
core.
In the Aquitaine, K. SZTRAKOS investigated benthic foraminifera
from numerous boreholes. The Cuisian alveolinid faunas recovered
from these boreholes contain A. canavarii, a typical member of
the Mediterranean assemblages that complements the occasional
occurrences of mediterranean assilinid and alveolinid species
in the Lower Lutetian. This suggests that the Aquitaine, during
Lower and early Middle Eocene at least, was not a true marginal
basin but submitted to particular local environmental conditions
and calls for additional investigations of the facies in the Central
Pyrenees that contain higher contents of carbonate. The northern,
clearly marginal basins in Belgium show occasional incursions
of low-diverse, often monospecific nummulite faunas currently
under investigation by J. BACCAERT (28).
5. The limits between Late Eocene and Oligocene, with the substitution
of the orthophragminids by the lepidocyclinids as well as the
Oligo-Miocene have again entered in the focus of biostratigraphical
research on larger foraminifera. During the last 2-3 years, the
larger foraminifera (mainly Nephrolepidina, Eulepidina and Miogysinids,
but also all the nummulitids) of the Oligocene and the early Miocene
were sampled from shallow-marine successions located in SW Turkey
(successions overlying the early Tertiary units of the Bey Da_larĶ
carbonate platform between Denizli and Antalya), in the Sivas
Basin in central Turkey and in the Mu_ Basin in eastern Turkey.
Whenever possible, pelagic faunas and floras have also been studied
and integrated. The evolutionary scheme for Nephrolepidina proposed
in European localities is not totally applicable here since the
early Miocene specimens have quite primitive features (in the
Sivas and Mu_ basins). The Mu_ basin provided a continuous section
with about 20 successive horizons with larger foraminifera of
Rupelian to Chattian age (29).
A moderately diverse larger foraminiferal fauna from the north-eastern
Italian ‘Arenarie e calcari di S. Urbano’ formation
with important stratigraphic, palaeoecologic and palaeobiogeographic
implications is described with respect to its position from the
Western Tethys area. The presence of Archaias hensoni SMOUT and
EAMES shows that some members of the much more diverse Middle
Eastern associations of shallow water larger porcelaneous foraminifera
are also present in the north-western parts of the Western Tethys.
This reveals the presence of a diversity gradient among larger
foraminiferal faunas in the Western Tethys that may be related
to a decrease in temperature along a geographical gradient (30).
6. Paleobiogeography: A significant and consistent paleobiogeographic
analysis of the Paleogene larger foraminifera needs a paleogeographic
base with sufficient details to map climatic gradients and oceanic
current patterns to be correlated with the distribution patterns
of the taxa. Usually, we have to operate on the species level
in order to get significant results. The taxa have to be conceived
in a way that is consistant at least within the group considered.
The first attempts in this direction are still rather far from
satisfactory (31, 32).
7. Structural analyses and functional morphology of Paleogene
larger foraminifera: Comparative anatomy and structural analysis
need a standartised vocabulary to designate the structural elements
in a consistant way. Therefore, an illustrated glossary was prepared
and presented at the Forams 2006 congress in Brazil (33, 34).
The functional significance of the "face" of selected
benthic foraminifera (35), of ornamental features such as papillae
as collectors of light for the symbiosis (36) and the meaning
of meandrine structures repeated in unrelated groups of larger
forams (37) were investigated. J. BARTHOLDI presented his thesis
on the structure of Nummulites in 2002 (38) where such meandrine
structures are frequent.
References:
1. LESS, G., ÖZCAN, E., PAPAZZONI C.A. & STOCKAR, R.
in press. – Middle to Late Eocene evolution of involute
Heterostegina, nummulitid Foraminifera, in the Western Tethys.
– Acta Palaeotol. Polonica.
2. LESS, G. & ÖZCAN, E. in press. - Late Eocene evolution
of Spiroclypeus, nummulitid Foraminifera, in the Western Tethys.
- Acta Palaeontol. Polonica.
3. ÖZCAN, E., LESS, G., BALDI-BEKE, M., KOLLANY, K., &
KERTESZ, B. 2007.- Biometric analysis of Middle and Upper Eocene
Discocyclinidae and Orbitoclypeidae (Foraminifera) from Turkey
and updated orthophragmine zonation in the Wesren Tethys. micropaleontology
52: 485 – 520.
4. LESS GY., ÖZCAN, E., BÁLDI-BEKE M. & KOLLÁNYI
K. (2007): Thanetian and early Ypresian orthophragmines (Foraminifera:
Discocyclinidae and Orbitoclypeidae) from the central Western
Tethys (Turkey, Italy and Bulgaria) and their revised taxonomy
and biostratigraphy. Rivista Italiana di Paleontologia e Stratigrafia,
113, 3, 419–448.
5. SIREL, E. 2004.- Türkiye'nin Mesozoyik ve Senozoyik Yeni
Bentik Foraminiferleri. – Ankara (TMMOB Jeoloji Mühendisleri
Odasi 84), 219 pp. 66 pls.
6. ÖZCAN, E., LESS, G. & KERTESZ, B. 2007.- Late Ypresian
to Middle Lutetian Orthophragminid record from Central and Northern
Turkey: Taxonomy and remarks on zonal scheme. – Turkish
J. Earth Sciences 16: 281 – 318.
7. LESS GY. & Ó. KOVÁCS L. (in press): Typological
versus morphometric separation of orthophragminid species in single
samples – a case-study from Horsarrieu (upper Ypresian,
SW Aquitaine, France). Revue de Micropaléontologie
8. HOTTINGER, L. 2007.- Revision of the foraminiferal genus Globoreticulina
RAHAGHI, 1978, and of its associated fauna of larger foraminifera
from the late Middle Eocene of Iran. Notebooks on Geology (Brest),
CG2007-A06, pp. 1-51, 3 Figs., 15 Pls.
9. SAMEENI. S. J. & BUTT, A.A. 2004.- Alveolinid biostratigraphy
of the Salt Range succession, Northern Pakistan. Revue Paleobiologie,
23(2):505-527 and corrigendum—ibid. 2005 - 24(2): 803-805.
10. GHAZI, S., BUTT, A.A. & ASHRAF, M. 2006.- Microfacies
analysis and diagenesis of the Lower Eocene Sakesar Limestone,
Nilawahan Gorge, central Salt Range, Pakistan. Jour. Nepal Geol.
Soc., 33: 23-32.
11. DROBNE, K., OGORELEC B. & RICCAMBONI, R. 2007.- Bangiana
hanseni n. gen. n. sp. (Foraminifera), index species of Danian
age (Lower Paleocene) from the Adiatic carbonate platform in SW
Slovenia, NE Italy and Herzegovina. - Razprave IV. Razreda SAZU
(Ljubljiana). 48: 5-71, 31 Figs., 12 Pls.
12. OGORELEC, B., DROBNE, K., JURKOV_EK, B., DOLENEC, T. &
TOMAN. M. 2001.- Paleocene beds of the Liburnia Formation in _ebulovica
(Slovenia, NW Adriatic – Dinaric platform). Geologija, (Ljubljana),
44/1, 15 – 65, 12 Figs., 11 Pls.
13. TISCHLER, M. & HOTTINGER, L. in preparation.- Paleogene
larger foraminifera from the carbonate sediment cover of the Preluca
Massif and the Radua Horst (Rumanian Carpathians).
14. SARTORIO, D. & HOTTINGER, L. in preparation. - Neorhipidionina
uranensis (Henson), a Middle-Eastern porcelaneous foraminifer
on the Apulian carbonate platform.
15. VECCHIO, E., BARATTOLO, F. & HOTTINGER, L. 2007.- Alveolina
horizons in the Trentinara Formation (Southern Apennines, Italy):
stratigraphic and paleogeographic implications. Rivista Italiana
Paleontologia e Stratigrafia Vol. 113/1, pp. 21 - 42.
16. VECCHIO, E. & BARATTOLO, F. 2006.- Periloculina (?) decastroi
n. sp., a new foraminifer from the Eocene (uppermost Ypresian
- lowermost Lutetian) Trentinara Formation (southern Apennines,
Italy). BARATTOLO F. & VECCHIO E. Eds., Paleontology and stratigraphy
in the Mediterranean palaeogeography, Naples, 20-21 June 2005.
Bollettino della Società Paleontologica Italiana Vol. 45/1,
pp. 147-158.
17. VECCHIO, E. & HOTTINGER, L. 2007. – Agglutinated
conical foraminifera from the Lower-Middle Eocene of the Trentinara
Formation (southern Italy). – Facies (Erlangen), 53/4: 509
- 533.
18. BASSI, D. 2005a. – Larger foraminiferal and coralline
algal facies in an Upper Eocene storm-influenced, shallow water
carbonate platform (Colli Berici, north-eastern Italy). Palaeogeography
Palaeoclimatology Palaeoecology, 226: 17-35.
19. BASSI, D. 2005b. – The Upper Eocene crustose coralline
algal pavement in the Colli Berici, north-eastern Italy. Annali
Univ. Ferrara, sez. Museologia Scientifica e Naturalistica, vol.
spec.: 63-74.
20. BARATTOLO, F., BASSI, D. & ROMANO, R. 2007.- Upper Eocene
larger foraminiferal-coralline algal facies from the Klokova Mountain
(Southern continental Greece). Facies, 53: 361-375.
21. NEBELSICK, J.H., RASSER, M. & BASSI, D. 2005. –
Facies dynamics in Eocene to Oligocene circumalpine carbonates.
Facies, 51: 197-216.
22. ZAKREVSKAYA, E.YU. 2004a. - On “Paleocene” Nummulites
from Mangyshlak. - Paleontological Journal. Moscow: Nauka. 38,
No. 5: 469 – 478 (in English).
23. ZAKREVSKAYA, E.YU. 2004b. - Distribution of larger foraminifera
near the Lower-Middle Eocene boundary in the Northeastern Peritethys.
- N. Jb. Geol. Paläont. Abh., Stuttgart, 234 (1-3): 335-360
24. ZAKREVSKAYA E.YU. 2007. – The late Paleocene species
Discocyclina seunesi Douv. in the Eastern Crimea. Paleontological
studies in Ukraine: history, present-day state and prospects.
Sbornik nauchnykh trudov IGS NASU. Kiev. pp. 228-232. (in Russian)
25. ZAKREVSKAYA, E.YU. 2005a. - Stratigraphic distribution of
Larger Foraminifera in the Paleogene of Northeastern Peritethys.
- Stratigraphy and Geological correlation, 13, No. 1: 59-79 (in
English)
26. ZAKREVSKAYA, E., STUPIN, S. & BUGROVA, E. in press - Larger
foraminiferal distribution in Eocene hemipelagic deposits of the
Western Caucasus (Southern Slope) and their correlation with planktic
foraminifera. – Spec. Number of Geologica Acta. (Intern.
Meet. Climate and biota of the early Paleogene, Bilbao, June 2006).
27. ZAKREVSKAYA E.YU. 2005b. – The regularities of larger
foraminifera distribution in Paleocene-Eocene. - Micropaleontology
in Russia on a boundary of centuries. Proceeding vol. Moscow,
2005. P. 20-21. (in Russian)
28. BACCAERT, J. 2007.- Analysis of some nummulite populations
of the Belgian Early Eocene and (re)determination of their taxa.
Abstract RCNNS meeting Krakow, Sept. 07.
29. ÖZCAN, E., LESS GY., BÁLDI-BEKE M., KOLLÁNYI
K. & ACAR, F., Oligo-Miocene Foraminiferal Record (Miogypsinidae,
Lepidocyclinidae and Nummulitidae) from the Western Taurides (SW,
Turkey): biometry and implications for the Regional Geology: Journal
of Asian Earth Sciences (in review).
30. BASSI, D., HOTTINGER, L. & NEBELSICK, J.H. 2007. –
Larger foraminifera from the Late Oligocene of the Venetian area,
north-eastern Italy. Palaeontology, 50: 845-868.
31. DROBNE, K. & HOTTINGER, L. 2004. – Larger Miliolid
Foraminifera in Time and Space. – Bulletin Academie Serbe
Sciences et Arts, Sciences Naturelles no. 42: 83 – 99.
32. BASSI, D., CIRILLO, S., NEBELSICK, J.H., HOTTINGER, L. &
BRAGA, J.C. in preparation. – Oligocene diversity patterns
in larger foraminifera: perspectives to Tethyan palaeobiogeography.
33. HOTTINGER, L. 2006.- Illustrated glossary of terms used in
foraminiferal research.- Notebooks on Geology, Brest, Memoir 2006/2,
126 p. 83 figs. Electronic publication: http://paleopolis.rediris.es/cg/uk_index.html_MO2
pdf 1- 4.
34. BASSI, D., FUGAGNOLI, A. & HOTTINGER, L. 2006. –
Foraminiferal shell structures – 1st and 2nd part. Annali
dell’Università degli Studi di Ferrara, sez. Museologia
Scientifica e Naturalistica, vol. 2 (1). http://eprints.unife.it/annali/museologia/vol2.htm
35. HOTTINGER, L. 2006.- The "face" of benthic foraminifera.
Bolletino Società Paleontologica Italiana (Modena) vol.
45 (1): 75-89.
36. HOTTINGER, L. 2006.- The depth-depending ornamentation of
some lamellar-perforate foraminifera. Symbiosis vol. 42: 141 -151.
37. HOTTINGER, L. 2005.- Geometrical constraints in foraminiferal
architecture: consequences of change from planispiral to annular
growth. Studia geologica polonica 124: 99-115.
38. BARTHOLDY, J. 2002.- The Architecture of Nummulites (Foraminifera)
reexamined. – PhD thesis Freie Universität Berlin.
64 pp., 22 figs,. 16 pls.
Report by Lukas Hottinger, Chairman of the Larger Foraminifera
Working Group.
|