Bollettino SPI Vol. 22 - Issues 1-2, 3

Issues 1-2

Published in April 1984

  • Pantić N., Grubić A. & Sladić-Trifunović M. (1983)

The importance of Mesozoic floras and faunas from intraoceanic carbonate platforms for interpretation of palaeogeographic and geodynamic events in the Tethys

pp. 5-14

Abstract

The analysis of palaeophytogeographic situations and the analysis of the distribution and migration of shallow water faunas during the Jurassic and the Cretaceous are given based on considerations of Mesozoic continental flora and oceanic fauna from shallow water deposits of West Tethyan intraoceanic carbonate platforms. A tropical Tethyan phytogeographic realm is separated; its characteristics, and particularly the tracing of changes in it, compared to the situations in Gondwana and Laurasian phytogeographic realms, give much new information for understanding geodynamic processes in the Tethys (horizontal movements, troughs as some kind of barriers, etc.). Similar analysis is given for shallow water faunas, whose occasional expansion is associated with changes in climate (contraction or expansion of tropical and subtropical climatic belt). Using all the available data, Mesozoic Tethys can be reconstructed as a very complex basin bounded by continental shelfs (African and Euro-Asian), and with carbonate platforms, islands and other archipelagos between them, separated sometimes by very deep troughs which seldom had the oceanic crust.

  • Pavlovec R. (1983)

Paleoecology of Nummulitines

pp. 15-19

Abstract

Data on the genesis of nummulitic beds («bancs à Nummulites») are still very incomplete. The majority of authors maintain that nummulites are benthonic animals of shallow and warm sea. Considering their way of life some researchers are conviced that they lived in the vertical position in the bottom mud, while others favour the idea they lived on marine plants. The observations of living nummulitins and related foraminifers tend to support the latter hypothesis. The ideal model of P. Arni postulates nummulitic beds on the outer margin of the continental platform. This scheme worked out on the basis of observations on the African platform does not suit in all parts of the shallow Tethys area, as already remarked by several authors. In the majority of recent discussions on the genesis of the nummulitic beds the following problems have not been considered with sufficient clarity:
— When occurs in the nummulitic beds a genuine biocenose (or better a paleobiocenose), and when a thanatocenose;
— Are the observed beds really from entirely synchronous horizons, or do exist between them smaller time differences;
— The abundance of macroforaminifers depends quite often more on sea plants and slight ecological differences than on the
depth of the sea; attention to this was called during investigations in the Red Sea by L. Hottinger, and it holds true possibly also for particular species of nummulites, operculinas and assilinas.
In western parts of the Outer Dinarides often indications were found by us of short range redeposition of nummulitins in nummulitic beds. In many beds occur mixed nummulites, alveolinas and other large foraminifers.
In western Yugoslavia the continental platform became intensively deformed during Paleocene and Eocene in course of orogenic movements. The uplifting progressed from northwest towards southeast. In front of the rising parts existed flysch basins.
South of the flysch basins remained the platform on which the nummulitic beds were deposited. From the platform numerous nummulitins came into the flysch sea, especially into the flysch olistostromes.
The least data are available on paleoecological differences between the nummulites, assilinas and operculinas. From differences in abundance of these genera in different beds smaller differences in the way of life of these genera can be inferred.

  • Peypouquet J.P. (1983)

Paleobathymetry and paleohydrology study based on ostracods in the Kef section (North Eastern Tunisia) between Maastrichtian and Ypresian stages

pp. 21-29

Abstract

An ostracod study carried out in the Kef section by Donze et al. (1982) helped to determine the classification of the fauna met, point out their stratigraphic interest, show the paleogeographic relationship among certain species, bring into light the general aspect of the environment.
In this paper, particular attention is paid to the paleobathymetric and paleohydrological evolution of the site between Maastrichtian and Ypresian stages.
1°) As far as the first point is concerned, the site evolves between an epibathyal domain than that of an outer shelf within the lapse of time considered.
2°) Krithe and Parakrithe used to the Peypouquet methods (1977-1979) helped to study the intensity and height of a minimum oxygen zone, deduce the major hydrological result during the Cretace-Tertiary transition and finally set a hypothetical evolution pattern concerning hydrological structures which occur later on.

  • Piccoli G. & Savazzi E. (1983)

Five shallow benthic mollusc faunas from the Upper Eocene (Baron, Priabona, Garoowe, Nanggulan, Takashima)

pp. 31-47

Abstract

Five benthic mollusc faunas from the Upper Eocene are put into comparison. Three of them belonged to the Tethys domain (Priabona, NE-Italy; Garoowe in Somalia; Nanggulan in Java, Indonesia); two were situated at its margins or outside it (Baron in the Paris basin, France; Takashima near Nagasaki in the Kyushu Island, Japan). The possible palaeoequator in Upper Eocene is inferred. An attempt is made of a mathematical elaboration of the faunal comparison.

  • Pleničar M. (1983)

The living environment of the Cretaceous fauna in the Northwestern Dinarides

pp. 49-51

Abstract

Important for Cretaceous organisms in the southwestern part of the northwest Dinarides is a carbonate platform which was accompanied in the northeast by a pelagic turbiditic flysch myogeosynclinal trough. This trough was rimmed on its northwestern side by an island arc beyond which were situated the lagoonal area and, still farther, the land. The carbonate platform was in existence since Triassic, and began to break in parts at the end of Cretaceous. According to recent authors, the carbonate platform was represented by the Adriatic plate which was moved under the influence of the African craton towards the east and northeast. Due to collision of the Adriatic and Pannonian plates subduction phenomena occured, as well as uplifting of marginal parts of the Adriatic plate. According to Polak, these marginal parts emerged also above the sea level, as indicated by bauxite deposits, or formed shallow thresholds on the sea bottom. In parts covered by shallow seas, conditions were favorable for the appearance of the reef fauna, which is considered in the present study.

  • Poluzzi A. & Forti P. (1983)

Substrata, areal distribution and competitive interaction of some Cheilostomatous Bryozoa from the Po River Delta plain

pp. 53-64

Abstract

The study area extends beyond the distributary channel named Po di Levante and consists of several, closely spaced lagoonal ponds («Paludi») and brackish coastal lakes («Valli»). The former are in contact with the open sea, the latter are closed basins with stagnant waters. Cheilostomatous Bryozoa were gathered in three major hard substrata such as aggregates of tube dwelling Polychaetes, boulders of artificial piers and acquatic weeds (Ruppia spiralis, Phragmites communis and Cystoseira sp.).
Field evidences suggests that the space-limited deltaic system is characterized by competitive framework in which the identified Bryozoa, due to their morphological and life-history attributes, should play a role of dominance owergrowing spatial antagonists of the hard substrata. In contrast, the distributional pattern of Bryozoa appears largely conditioned by direct or mediate influence of physical factors. Density estimates in lagoonal boulders show that under conditions of high sedimentary supply and of desiccation after low tides, there is a nearly complete exclusion of Bryozoa by other solitary and colonial animals. Further, in boulders subsurface of coastal lakes, where reducing conditions, here expressed by the redox potential, act as a threshold against the great majority of sedentary organisms, Conopeum seurati and Electra monostachys have an aggregative settlement and monopolize almost the entire substrata. In this contest the redox potential of various substrata seems appropriate to account for the dominance and the outcome in the interaction of two or more species of Bryozoa.

  • Reato S. (1983)

Palaeoecological meaning of Upper Eocene mollusc fauna from the Marna di Possagno Formation (Treviso, NE Italy) among shallow benthic Tethys faunas

pp. 65-75

Abstract

The palaeobiological meaning of the mollusc fauna from Possagno (Upper Eocene) is considered.
The variations of the mollusc faunas from the Upper Eocene are put into relationships with the environmental changes due to the geodynamic events in that part of the Paleogene Tethys.

  • Sahni A., Bhatia S.B. & Kumar K. (1983)

Faunal evidence for the withdrawal of the Tethys in the Lesser Himalaya, Northwestern India

pp. 77-86

Abstract

The Subathu Formation of the Lesser Himalaya represents the last phase of the Tethys in northwestern India. The Subathu sediments show a progressive continentality in sedimentation from the basal beds to the topmost red bed sequence. This regressive phase is documented both on lithological criteria and facies variation as well as on palaeontological evidences. Faunal assemblages represented by vertebrates (fishes, turtles, crocodiles and mammals) and the invertebrates (foraminifera, ostracods, molluscs and bryozoans) record the shallowing of the remnant tethyan basin.

  • Savazzi E. (1983)

Constructional morphology of cardiid bivalves: an overview (Konstruktions – Morphologie Nr. 142)

pp. 87-91

Abstract

Within the Cardiidae, extremely varied sculptural patterns contrast with evolutionary conservatism of other morphological characters. Most sculptural features can be interpreted as burrowing sculptures, and this accounts for part of the morphological convergences between different groups. However, there appears to be no univocal relation between particular types of sculptures, burrowing mechanisms and sediment types. In most cases, the microstructure of sculptural features seems to be of better taxonomic value than the general aspect of the sculptural pattern.

  • Schaub H. (1983)

Paleogene Tethys, domain of Nummulites

pp. 93-102

Abstract

Neritic sediments of the Paleogene Tethys can be dated by Nummulites and Assilina. Species of these genera can be used as markers for stages and biozones, if we know to which phyletic series they belong.
If correctly determined, those species do not only indicate the age of their beds and make correlation on long distances possible, but they mark also the zone of the shelf bordering the Tethys.
Nummulites found in the coarse-grained basal parts of turbiditic sandstone layers of flysch or in coarse-grained flyschoid intercalations in pelagic series inform us about their transport from neritic to bathyal parts of the Tethys.
When comparing nummulitic faunas from northern parts of Tethys (e.g. Pyrenees, Alps, Crimea, Iran) with faunas of the same age from the southern border of the Tethys (Northern Africa), we observe differences in faunal composition indicating that during much of the time, those regions were separated by a large non-neritic zone which could not be crossed by Nummulites and Assilinas. However, crossing was possible locally and for short periods of time.

  • Scudeler Baccelle L. & Marusso F. (1983)

Trace elements in Cenozoic Algal Limestones of the Venetian Region: Mn2+– Sr2+ negative correlation

pp. 103-107

Abstract

Cenozoic rhodolites from Veneto region are studied from the geochemical viewpoint, taking into consideration the Mg2+, Sr2+, Fe2+ and Mn2+ contents. The Cenozoic rhodolites presently consist of low-Mg calcite (LMC); they have lower Sr2+ and Mg2+ contents and higher Mn2+ and Fe2+ contents with respect to the modern nodules. This situation support the hypothesis that the Cenozoic rhodolites analysed were originally composed of high-Mg calcite (HMC), which altered into LMC during meteoric diagenesis. The chemical behaviour and in particular the negative correlation between Sr and Mn, are consistent with the model of meteoric diagenesis recently proposed by Pingitore (1978) and Brand & Veizer (1980).

  • Sorbini L. (1983)

The fossil fish fauna of Bolca and its biogeographical relationship with the living specimens

pp. 109-118

Abstract

A number of findings drawn mainly — but not solely — from the Eocene fossil beds of Bolca in Northern Italy are presented within the
framework of the debate existing between dispersal vs vicariance biogeographers.
The fish fauna of Bolca is represented by 180 genera, 61 of which have been re-examined during the last few years. Out of these 61 genera, 22 can be considered similar to specimens now living. By this we mean that the osteological changes which took place during more than 50 million years have been of minor import, which allows us to believe that a close phylogenetic kinship may exist between the Eocene fish specimens and their corresponding existing ones.
If we consider the biogeographical affinities between the 22 genera from Bolca on one side, and the 22 actual genera that are osteologically similar on the other, we see that all of the latter ones are now living in the western Indo-Pacific biogeographical region, but 14 genera are living also in the tropical or sub-tropical Atlantic, and some even in the Mediterranean.
On the basis of such findings, the old concept of a close biogeographical affinity between the fish fauna of Bolca and that of the Indo-Pacific Ocean should be modified and extended on account of the fact that a considerable number of present genera similar to the Bolca ones are available in the warm waters of the Atlantic.
The distribution then, assumes the character of a general track, on account of its being represented by a large number of genera, and is probably in connection with Tethys, thus dating back to a much earlier time than is expected.
In the study of the distribution of actual species, both similar among them or similar to the fossil ones, one conclusion seems to be inferred by the great majority of cases examined to wit, the present area is the result of a former and much wider one to which the old species belonged. This area was then split by barriers produced by geodynamic and climatological events, which agrees with the vicariance biogeographers’ hypothesis. Additional factors such as climatic changes, sea level changes and biological competition later accounted for the extinction of some species in some areas. However, at least in one case (vz. Lates from Africa) it is possible to spot along the coasts of northern Africa the point of origin of the species which colonized the African inland waters proceeding along a North-South direction, which would give credit to the dispersal biogeographers’ hypotheses. 

  • Strougo A. (1983)

The genus Carolia (Bivalvia: Anomiidae) in the Egyptian Eocene

pp. 119-126

Abstract

The earliest known occurrence of the genus Carolia is in the Lower Eocene, when it appeared simultaneously in Senegal, Egypt and Pakistan. After a period of rapid expansion during the Middle Eocene, it declined in the Upper Eocene and became extinct by the end of that time. In Egypt, where its record is most complete, Carolia is represented by five species and one subspecies distributed into six successive stratigraphic levels. From a common parent stock — Carolia blanfordiana — two lineages emerged. The first, the Wakullina (Huyella) lefevrei lineage, is characterized by progressive suppression of byssal attachment and development of a secondary hinge line; the second, the Carolia placunoides lineage, more conservative, retained the byssus for longer time. The Pododesmus-like Carolia libyca represents a side-branch of the main stock. A small anomiid — Tarturia quaasi n. gen., n. sp. — from the Maastrichtian of Egypt may have given rise to Carolia in the Eocene.

  • Tassos S.T. (1983)

Organic matter and clay minerals in the bottom sediments of Kalloni Bay Lesvos Island, Greece

pp. 127-133

Abstract

The total organic matter content in the bottom sediments of Kalloni Bay is 7.40% of dry weight. Average values of 11.6 ppm, 4.90 mg/g and 0.05% have been found for pheophytin, total carbohydrates and lipids, respectively.
A positive relationship between montmorillonite – illite ratio, and total organic matter content has been found.

  • Tassos S.T. (1983)

Marine Holocene foraminifera and ostracoda from Kalloni Bay, Lesvos Island, Greece

pp. 135-144

Abstract

The foraminifer Elphidium and the ostracod Loxoconcha dominate the bay microfauna and are characteristic of the euryhaline and shallow water environment of Kalloni Bay. General bay, upper and lower bay biofacies have been recognized.

  • Tassos S.T. (1983)

Geodynamic evolution of the Aegean Region

pp. 147-150

Abstract

The synchronous uprising of magma in the north Aegean and the gravitational compression due to spreading in the Atlantic, Indian and Pacific Oceans, as well as the sinistral Tethyan megashear, determine the geodynamic evolution of Tethys and of the Aegean region.
In the south Aegean the well defined Benioff zone is due to the underthrusting of the African continental lithosphere, while the weak north Benioff zone is due to the uprising mantle.

  • Huang T. (1983)

Foraminiferal biofacies of the Taiwan Strait, ROC

pp. 151-177

Abstract

The Taiwan Strait is about 500 km long and 150 km wide, with water depths ranging down to 150 m.
The bathymetry of the area studied and the Penghu Islands, the Taiwan Bank, the Taichung Bank, the Penghu Basin, the Matsu Basin, the Penghu Channel, and the Chilung Channel are recognizable in the area.
Three major currents occurs in the area; the Kuroshio Current, the China Coastal Stream, and drift due to monsoon in the South China Sea. Oceanographic observations, sediment, and other features in the strait of the different seasons are described.
Ninety sediment samples were taken in the Taiwan Strait to study distribution of the planktonic and the benthonic foraminifers. More than 400 species of the benthonic foraminifers and 27 species of the planktonic foraminifers were found in the strait and were used for the analyses.
The high density of the foraminifers is in the Matsu Basin and near the edge of the shelf off the coast of northern and southern Taiwan.
The distribution of planktonic foraminifers is controlled by the topography and the current action and the high density in the Penghu Channel and the Chilung Channel areas. The cool-water species are abundant in the north half of the strait and warmwater species are abundant in the south half.
Six foraminiferal facies were determined: (1) the near-shore facies (less than 40 m), characterized by predominant Pararotalia ozawai and P. taiwanica in the assemblage, with reworked worn specimens common; (2) the offshore facies along the west side of near-shore facies (40-100 m), characterized by mixed occurrences of the near-shore and basin facies with Textularia conica abundant in the assemblages; (3) the basin facies (60-100 m) in the central portion of the strait and along the west side of the offshore facies, characterized by the dominant occurrence of Bolivina robusta pacifica; (4) the bank facies in the area near the Taiwan Bank (20-150 m), characterized by the dominance of Cibicides pseudoungerianus and Cibicides sintikuensis together with Pararotalia and miliolids; (5) the Chilung Channel facies (50-150 m) near the Chilung Channel, characterized by the Cibicides pseudoungerianus – Asterorotalia inflata assemblage; and (6) the Penghu Channel facies (100-200 m) in the Penghu Channel, characterized by an association of rather deep water forms, including Bolivina, Bulimina, Cassidulina, Gyroidina, Hanzawaia, Siphogenerina, and Uvigerina.
For an attention for faunal diversity, four different index are measured. The result correlated well with the facies distribution and topography of the strait.

  • Wen Y. (1983)

Cretaceous Gastropod Assemblages from Xizang (Tibet) with reference to their paleozoogeographical significance

pp. 179-183

Abstract

The Cretaceous marine gastropods are mainly distributed to the north and south of the Yalung Zangbu River, characterized by having Nerineids as their principal element. Based on gastropods and their associated fossils, the assemblages of Xizang bear a similarity to those of Europe, Middle East, Baluchistan as well as Kashmir, all belonging to the Indo-Mediterranean Region of Tethyan Realm.

Issue 3

Published in November 1984

  • Mainelli M. (1983)

Nuove Rudiste del Cretacico inferiore – medio di monte La Costa (S. Polo Matese, Campobasso)

pp. 189-208

Abstract

Si descrivono le seguenti nuove Rudiste rinvenute nei calcari organogeni di monte La Costa, nel comune di S. Polo Matese (Campobasso): Schiosia nicolinae n. sp. dell’Aptiano superiore; Schiosia paolae n. sp. del Cenomaniano superiore; Toucasia danielae n. sp. del Cenomaniano superiore.
Le Schiosia si distinguono nei caratteri dei canali palleali; hanno ognuna forma generale singolarissima; il genere con S. nicolinae si rinviene per la prima volta nell’Aptiano.
Toucasia danielae, il cui genere viene segnalato per la prima volta nel Cenomaniano, si distingue nei caratteri delle valve spirali coniugate ed in particolare in quelli della valva fissa.

  • Coccioni R. (1983)

Foraminiferi planctonici miocenici anomali nella Scaglia Rossa Umbro-Marchigiana

pp. 209-224

Abstract

Foraminiferi planctonici di età langhiana (Miocene medio) sono stati ritrovati in alcune intercalazioni marnose della Scaglia Rossa (Cretacico superiore-Eocene medio) dell’Appennino umbro-marchigiano. I risultati di questo studio mettono in evidenza l’estraneità dei foraminiferi miocenici alla formazione e suggeriscono l’ipotesi di una contaminazione di tipo tettonico di materiale delle formazioni dello Schlier, del Bisciaro e della Scaglia Cinerea.

  • Taddei Ruggiero E. & Ungaro T. (1983)

Sardorhynchia crassa gen. nov., sp. nov. (Brachiopoda), from Jurassic of Sardinia

pp. 225-246

Abstract

In this work the new genus Sardorhynchia is instituted with S. crassa sp. nov. from Upper Bathonian-Callovian of the Nurra (N-W Sardinia) as type species. This paper provides also a study of the ultrastructure of both shell and inner structures as they appear at the S.E.M., while similarities with and differences from other members of the same subfamily Tetrarhynchiinae are discussed. A hypothesis is put forward concerning the ways of life of the adult and young individuals.

  • Ciampo G. (1983)

Alcuni ostracodi del Miocene superiore piemontese

pp. 247-262

Abstract

Vengono descritte 14 nuove specie di ostracodi del limite Tortoniano/ Messiniano provenienti dalle sezioni
di Rio Mazzapiedi e S. Agata Fossili (Piemonte). Vengono inoltre discusse alcune specie già note in letteratura.

  • Pittau Demelia P. (1983)

Stellapollenites muelleri (Reinh & Schmitz, 1965) n. comb. and Podocarpeaepollenites thiergartii (Madler 1964), two different Triassic pollens: observations under light and scanning electron microscope

pp. 263-269

Abstract

Two species belonging to different genera: Stellapollenites muelleri n. comb. and Podocarpeaepollenites thiergartii are re-described. Observations under scanning microscope allows to show the monosaccate nature and the relationship between the proto (?) monosaccus and the body of S. muelleri n. comb.

  • De Giuli C. & Masini F. (1983)

A new element of the Late Villafranchian (Tasso Unit) faunas of Italy: occurrence of Ovibovini (Bovidae, Artiodactyla, Mammalia) in the fauna of Casa Frata (Upper Valdarno, Tuscany)

pp. 271-280

Abstract

The occurrence of Ovibovini cf. Praeovibos in a Late Villafranchian fauna of Tuscany has been recognized. This taxon was not known in any Villafranchian fauna of Europe. Taxonomic characters of European Ovibovini are shortly discussed.

  • Ruggieri G. (1983)

Su alcuni Ostracodi illustrati nello “Stereo-Atlas”

pp. 281-286

Abstract

Vengono riesaminate alcune specie di Ostracodi marini neogeniche, pleistoceniche e recenti quali illustrate nello « Stereo-Atlas of Ostracod Shells ». Dal riesame emerge la possibilità di istituire alcune specie nuove, e precisamente Aurila fallax, Urocythereis nautae, Leptocythere mediorientalis, e un nuovo genere, Dorukella (specie tipo Orionina bireticulata Doruk).

  • Aruta L. & Ruggieri G. (1983)

Il genere Aurila (Ostracoda, Podocopa) nel Pleistocene inferiore di Olivella (Palermo)

pp. 287-295

Abstract

Vengono illustrati i rappresentanti del genere Aurila Pokorny 1955 nelle argille del Pleistocene inferiore (Emiliano?) di Olivella (Palermo). Sono istituite le nuove specie Aurila nana, A. elaborata, A. balanoides.

  • Ruggieri G. (1983)

Priorità del genere Rectotrachyleberis sul genere Costa (Ostacoda, Podocoplda)

pp. 297-299

Abstract

Il genere Costa Neviani, in quanto reso valido da Howe, 1955, risulta più giovane sinonimo di Rectotrachyleberis Ruggieri, 1952. Viene proposta una nuova specie, Rectotrachyleberis ciampoi, del Miocene superiore della Sicilia.

  • Sirna G. (1983)

Apricardia pachiniana, a new species from the Maastrichtian near Pachino (Southeastern Sicily)

pp. 301-303

Abstract

Apricardia pachiniana n. sp. a new species of the genus Apricardia is described. This species comes from the Maastrichtian limestones of the Pachino area (Southeastern Sicily).

  • Sartoni S. (1983)

Problemi e risultati delle ricerche compiute per la definizione dello stratotipo del limite Plio/Pleistocene

pp. 307-314

Abstract

Various problems and opinions concerning the definition of the Plio-Pleistocene boundary are briefly reviewed including the resolutions of the International Geologic Congresses of London (1948) and Algiers (1952). In the paper, the main results obtained by multidisciplinary researches carried out in the last years with the aim of establishing a workable definition of the Plio-Pleistocene boundary are reviewed as well. These researches, in which several Italian scholars have been involved, have brought to considerable advancements to the knowledge of biostratigraphy, magnetostratigraphy, radiometry and biochronology of the interval straddling the Plio-Pleistocene boundary.
Recently (Madrid, 1983) the INQUA Subcommission 1 d (P/P Boundary) and the ICS Working Group on the N/Q Boundary, in agreement with the Working Group of the IGCP Project No 41 (N/Q Boundary) officially proposed to the INQUA Commission on Stratigraphy the top of the marker bed «e» of the Vrica Section as the P/P Boundary-stratotype. This proposal should be approved by the Inter. Comm. on Stratigraphy during the next Inter. Geol. Congr. (Moscow, August 1984).
On July 15, 1983 the town council of Crotone issued a degree for the safeguard of the Vrica Section.

  • Ruggieri G. & Sprovieri R. (1983)

Recenti progressi nella stratigrafia del Pleistocene inferiore

pp. 315-321

Abstract

Recent proposals and improvements in the Chronostratigraphy, Biostratigraphy and Biochronology of the Lower Pleistocene are reviewed and discussed. The Selinuntian (Ruggieri and Sprovieri, 1979), originally erected as Superstage and now proposed at Stage rank, covers all the Lower Pleistocene, from the N/Q boundary at about 1.65 MA to the Lower/Middle Pleistocene boundary at about 0.8 MA, with a time-span of about
0.8 MA. The Selinuntian can be subdivided into three Substages, namely Santernian (Ruggieri and Sprovieri, 1976), Emilian (Ruggieri and Selli, 1950; Ruggieri et al., 1976, emended) and Sicilian (Doderlein, 1872; Ruggieri and Sprovieri, 1975, emended). The Calabrian (Gignoux, 1910, 1913), considered as junior synonym of the Sicilian substage, can no more be used in the Chronostratigraphic scale.

  • De Giuli C., Ficcarelli G., Mazza P. & Torre D. (1983)

Confronto tra successioni marine e continentali del Pliocene e Pleistocene inferiore in Italia e nell’area mediterranea

pp. 323-328

Abstract

1.1 – The zone, as defined in marine biostratigraphy, can not be identified dealing with continental faunas which have point distribution in space and time. Local Faunas are thus recognized in continental faunal sequences. Similar Locail Faunas make up a Faunal Unit which is defined by a type Local Fauna. Groups of Faunal Units form « Mammal Ages ». Boundaries among units can not be established and new units can be added in between.
Continental biostratigraphic criteria were discussed by Tedford, 1980 and Azzaroli, 1982. Tedford envisages Vertebrate Units as chronological entities drawn out of the embedding sediments, thus conceptually distinct from marine units that consist in rocks characterized by their paleontological content. There is no conceptual difference between biozone and faunal units since both are distinguished by the fossil content of rock bodies that are the expression of geologic time. The only but true difference is that the zone corresponds to a sedimentary continuum which enables the individuation of boundaries as physically existing surfaces. Faunal Units, instead, are not a sedimentary continuum in space and time, so boundaries are very difficult or, more often, impossible to be discriminated. Therefore correlations between continental and marine faunal sequences consist in projecting time segments, represented by the continental units, on the marine biostratigraphic scale.
1.2 – Still great confusion exists with regard to the established continental stratigraphies. Biostratigraphic scales in which faunal zones are distinguished by means of marine biostratigraphic statements applied to continental stratigraphy have been worked out. These subdivisions give a misleading impression of a continuous succession of faunal intervals.
2.1 – In the Italian Villafranchian « Mammal Age », the Triversa, Montopoli, Olivola, Tasso and Farneta Units can be distinguished. Other Italian local faunas, older and younger than the Villafranchian, can not stili be arranged in well defined faunal units. The pre-Villafranchian Local Faunas are Baccinello V3, Il Casino (upper lacustrine complex), Val di Pugna; the post-Villafranchian fossiliferous localities are far more numerous, but the exact chronological succession of most of them is still hard to establish.
The chronological gap between the Montopoli Unit and the Olivola Unit is covered by several French local faunas, such as Saint Vallier, Le Coupet and Chillac. Also the fauna of Tegelen, Holland, seems to be older than the one of Olivola. The Valle del Sacco and Collepardo (Anagni) fossil could stratigraphically be close to those of Saint Vallier.
2.2 – Baccinello V3 (Grosseto). The assemblage is characterized by Turolian (Tortonian p.p. – Messinian) forms together with elements that testify younger immigration events. Particularly meaningful is the occurrence of a leporid, indicated as aff. Hvpolagus, of a tapir and of a rhinoceros ascribed to Dicerorhinus  cf. megarhinus. The tapir testifies a return to umid climate as that of the Lower Ruscinian. The Baccinello V3 fauna represents the end of endemic conditions in Southern Tuscany and the final connection to the European continental area. Because of the association Baccinello V3 resembles Spanish, Libyan and South African local faunas that seem referable to the transition between the Turolian and the Ruscinian. Lorenz, 1968, assigns a Messinian age to the V3 level but the stratigraphy of Baccinello is still uncertain. Many correlations allow us to believe a correspondence of V3 with an initial phase of the marine Pliocene most probable.
2.3 – Il Casino – upper lignitic complex – (Siena). The faunal assemblage is poor; therefore detailed correlations with local faunas of the Mediterranean area are quite difficult. A Lower Ruscinian Age as that of the Montpellier Unit of Southern France can be inferred by the occurrence of Parabos cordieri and Sus minor, joined up with Tapirus arvernensis. The finding of Exaprotodon suggests a slightly older age than that of Montpellier. The relations with Baccinello V3 deserve deeper examination. Il Casino mammal deposits lie on gypsum beds ascribed to the Messinian or to part of it and underlie marine sediments assigned to the Globorotalia puncticulata Zone.
2.4 – Val di Pugna (Siena). The mammal fauna is very poor; anyhow the occurrence of Alephis lyrix and of a sirenid Felsinotherium gervaisi, more evolved than the Montpellier species, F. serresi, makes the correlation with the Perpignan Unit of Southern France most reliable. The mammal bearing marine sediments are referable to the Globorotalia puncticulata Zone. Suc, 1982, deems the Moltpellier and Perpignan faunas as belonging to a geologie horizon correlatable with the lower part of the Globorotalia crassaformis Zone. Taking in account also the stratigraphical data relevant to the following mammal units we believe more reasonable correlating the Perpignan Unit with the G. puncticulata Zone.

Significant macromammal local faunas between the Val di Pugna fauna and the following Triversa Unit faunal assemblage lack in Italy.
2.5 – Triversa Faunal Unit. The fauna comes from several sites along the Triversa and Triversola valleys nearby Villafranca d’Asti. Also the Local Faunas of Gaville and of the lignite mine of Santa Barbara, Upper Valdarno, of Barga and of Pieve Fosciana, in Garfagnana, and of Spoleto can be included into the Triversa Unit. Even the faunas of French localities, such as Vialette and Les Etouaires are surely referable to this same Faunal Unit. Baudet, Donville and Michaux assign to Vialette a radiometric age of 3.3 m.y. or younger, and anyhow not more recent than 2.6 m.y. In this lapse of time the paleomagnetic scale shows two negative events, Mammoth and Kaena, both comprised in the chrono-Gauss interval. Lindsay, Opdyke and Johnson, identified such negative events in the sediments that outcrop at one of the Triversa localities, Fornace RDB. Big size mammals suggest an increase of the forestal degrading that already began in the upper part of the previous unit. Such environmental alterations are well correlatable with the first climate cooling that took place about 3 m.y. ago. The Triversa continental deposits lie over, or, at least in part, laterally to the Pliocene marine sands of « Astian » facies that outcrop in the Asti area. Nearby Valleandona the occurence of Uvigerina cf. rutila was pointed out in a clayey level that underlies the « Astian » sands.
This Foram becomes extinct at the end of the G. puncticulata Zone in the Mediterranean basin. This datum also does not contradict the 3 m.y. assigned to the Triversa Unit.
2.6 – Montopoli Faunal Unit. It is essentially represented by the Montopoli (Pisa) Local Fauna, which must be considered the type fauna of the Unit. The Unit is characterized by the appearance of Equus and Mammuthus, while Zigolophodon and Tapirus seem disappeared. All this denotes a further forestal degrading and a marked increase of open spaces. The sediments that enclose the Montopoli mammals can be referred to the Middle Pliocene of Italian authors, that is to the Globorotalia crassaformis Zone.
According to several authors, the Triversa and Montopoli Units make up the Lower Villafranchian « Mammal Age ». However, because of their strong faunal change, faunal change clearly detectable at least in all Eurasia, it is advisable not to group these two Units into the same super-unit.
2.7 – Olivola Faunal Unit. It is characterized by the type Local Fauna collected at Olivola (Val di Magra) in an individual pocket of a fluvial deposit with thick gravel lenses. At Olivola, Canis etruscus and Pachycrocuta brevirostris are met for the first time in Italy. Some Upper Valdarno fauna were referred to the Olivola Unit; however, these are generally fossils of old collections with hagy indications relevantly to the collecting areas and without any geological reference. A Local Fauna that follows modern collecting criteria is that of Matassino; it is well correlable with the Olivola fauna. In order to date the Olivola unit, the fauna of Tegelen (Holland) should be taken under examination. The latter comes from clays with a Tiglian floral assemblage that comprises the Olduvai paleomagnetic event. The lack of genus Canis and of P. brevirostris, together with a higher primitivity of Mammuthus meridionalis and of Leptobos in the Tegelen fauna, lead to believe Olivola more recent. The migration of the dog and of the big hyaena could thus be related to the climatic cooling testified by the Eburonian flora that immediately follows the warm Tiglian phase.
2.8 – Tasso Faunal Unit. Only recently at Casa Frata near Terranova Bracciolini (Arezzo) a rich well representative fauna of the Tasso Unit assemblage was found. Therefore, the fauna of Casa Frata should be chosen as type Local Fauna of the Tasso Unit. The fauna novelties as a whole testify the persistence of degraded climatic conditions as those of the Eburonian phase. Thus the Tasso Unit is assumed correlatable with some interval of the upper part of the Globigerina cariacoensis Zone.
2.9 – Farneta Faunal Unit. This unit is not yet fully defined. It is used as gatherer of a group of faunas that come from various Italian localities (Selvella, Mugello, Imola, Crostolo, Leffe p.p., Gargano) that can generally be ascribed to the most recent phase of the Villafranchian. We can not tell if the Farneta Unit is still in the Eburonian phase or in a younger time. Mammals collected at Imola in littoral sediments overlying Hyalinea baltica bearing levels are referable to this unit. We can anyhow deem the Farneta Unit placed in a pre-Jaramillo phase since the French deposit of Le Vallonnet, characterized by a more modern fauna, showed a normai magnetisation referable to the Jaramillo event.
2.10 – Faunas just younger than those of the Farneta Unit are little known in Italy at present. The faunal renewal seems to pass through 3 following phases in which a progressive impoverishment of the Villafranchian facies components takes piace. In the first phase advanced Allophaiomys forms persist (Cava Sud and Viatelle near Verona, Monte Peglia in Umbria); the faunal assemblages are comparable with that of Le Vallonnet, mentioned above. In the second phase a micromammal fauna occurs devoid of Allophaiomys, with Mimomys savini and with macromammals mostly renewed but still with Villafranchian facies forms. The Italian Local Fauna that better exemplifies this second moment is that of Slivia. In the third phase the immigration of Arvicola takes piace; the Villafranchian facies forms are negligible. The Isernia fauna is typical of this period; radiometric dating and paleomagnetic surveys agree in assigning an age slightly older than 0.7 m.y.
In conclusion most of the faunal renewal in Italy seems to have occurred between 1.0 and 0.7 m.y. consistently with the Menapian cooling phase.