Bollettino SPI Vol. 21 - Issues 1, 2-3
Issue 1
Published in July 1983
- Laghi G.F. & Sirotti A. (1982)
 
Orbitoclypeus Silvestri, 1907: revision of the type-specimens
pp. 1-4
Orbitoclypeus Silvestri and Discocyclina Gümbel are two genera with a very close resemblance, but of different origin, as is indicated by the structures of the nepionic stages of the microspheric specimens and by a different arrangement of the stolons connecting the equatorial chambers.
The type specimens of Orbitoclypeus Silvestri are restudied and illustrated and the lectotype of Orbitoclypeus himerensis is proposed. Orbitoclypeus himerensis, type-species of the genus, is recognized as a junior synonymous of Orbitoclypeus nummuliticus (Gümbel, 1861).
A list is given of the European species belonging to the genus Orbitoclypeus, together with the stratigraphical range of the genus in Europe.
- Bonfiglio L. (1982)
 
SEM observations on the structures of Cancer sismondai Meyer
pp. 5-20
Twenty fragments of exoskeleton of Cancer sismondai Meyer have been examined with the scanning electron microscope. They come from carapace, abdomen and pereiopods of juvenile and adult specimens of both sexes. The skeletal components form a complicated architecture which has the basic structure of living Decapod Crustaceans. Nevertheless, some new observations were carried out. We distinguish three series of layers, which are from outside: layers of horizontal laminae, layers of vertical laminae alternating with horizontal laminae, layers of vertical laminae; vertical laminae are always curved both in horizontal and vertical sections; where they come into contact they form acute cusps. There is a gradual transition among the layers of different structures and the inner layers are thinner than the external ones. In the youngest specimens only layers of horizontal laminae are present. Layers of laminae arch below tubercles of pereiopods but they do not arch below tubercles of dorsal carapace. There is not an helicoidal arrangement of layers of laminae as suggested by Bouligand (1965, 1971). Vertical laminae do not emerge from both sides of each horizontal lamina as suggested by Mutvei (1974) but vertical and horizontal laminae are indipendent structures only associated in the intermediate layers of exoskeleton. We think that horizontal laminae can represent a primitive structure, while vertical laminae are a more evoluted structure. Epicuticle is preserved in some specimens and is constituted by pillars of horizontal laminae which have a loose structure, specially in the youngest specimens.
- Matteucci R., Schiavinotto F. & Ventura G. (1982)
 
Biometric research on the embryonal chambers of Nummulitids
pp. 21-33
Biometrical characters of the embryonic apparatus have been investigated in 10 species of Nummulitidae, belonging to 5 genera (Operculina custugensis, O. karreri, O. parva, O. schwageri, O. alpina, Nummulites planulatus, N. carpenteri, Assilina exponens, Spiroclypeus granulosus, Heterostegina sp.).
The relationships between the diameters of the first two chambers of megalosphaeric forms correlate well with the development of the second chamber by incomplete division of the first one before the formation of the calcareous wall, as shown by Rotiger & Spindler (1976) in Heterostegina depressa.
The sizes of the embryonic apparatus influence the characters of the spiral growth in the first two whorls in the species with an evolute test like those belonging to Operculina; that influence is very low or lacking in the species with an involute test (Nummulites and Spiroclypeus) or with a very rapid spiral growth (Heterostegina).
- Cafiero B. & de Capoa Bonardi P. (1982)
 
Biostratigraphy of the pelagic Triassic of Sicily
pp. 35-71
The pelagic sequences of the Triassic Sicano and Imerese basins of Sicily have been studied (fig. 1). Stratigraphic data of sicilian pelagic Triassic agree with those of other regions of Mediterranean area (Lucania, Southern Apennines; Dinarids, Yugoslavia; Pindos, Greece). The completest and richest in fossils of the studied successions, the M. Cammarata succession, is assigned to Julian – Upper Alaunian stratigraphic interval on the basis of Halobiids, of rare conodonts and very rare ammonites contained (fig. 2). A biostratigraphic correlation (fig. 3) is possible at various stratigraphic levels between M. Cammarata succession (Sicano basin) and M. Triona (Sicano basin), Capo Grosso (Imerese basin), M. Judica and M. Scalpello (eastern end of both basins) successions. Gemmellaro’s collection of Sicilian Halobiids, stored in Paleontological Museum of Palermo University, has been studied, and Gemmellaro’s species have been re-described.
Three new species are described: Halobia pusilla, H. rajkae, H. darwini.
Diagnosis of Halobia pusilla: Small, almost equilateral and circular shell. Prominents radial ribs, ear divided and posterior area without ribs.
Diagnosis of Halobia rajke: Large, inequilateral shell, with thin and subdivided radial ribs, prononced and divided ear, posterior area without ribs. 
Diagnosis of Halobia darwini: Large, subcircular shell, with low ear, submedian umbo, little subdivided radial ribs and wide anterior and posterior areas without ribs.
- Gnoli M. (1982)
 
Lower Devonian orthocone cephalopods from Iglesiente and Sulcis regions (Southwestern Sardinia)
pp. 73-98
A systematic description of the Lower Devonian orthocone cephalopods is given for the first time in the Mediterranean area. Twenty species pertaining to thirteen genera have been recognized among more than 300 specimens mostly collected by the author. Among the previously unreported forms, three are proposed as new: Hemicosmorthoceras semimbricatum, Kopaninoceras floweri and Orthocycloceras pseudoextensum. The species Jovellania buchi (De Verneuil) is discussed as a probable stratigraphical marker during the Lower Devonian.
As regards cephalopod faunal provincialism, the assemblage seems to signal a break in that relationship between Sardinian and Bohemian fauna already known for the Upper Silurian.
- Sirotti A. (1982)
 
Phylogenetic classification of Lepidocyclinidae: a proposal
pp. 99-112
The temporal succession and the analysis of the internal structures of the various taxa included in the family Lepidocyclinidae allow us to understand the possible phylogenetic relationships among the different genera. Two lineages seem to be distinguishable on the basis of the different location and number of the stolons connecting the equatorial chambers.
They characterize the two subfamilies Lepidocyclininae and Helicolepidininae more consistently than the formerly used characters.
The embryonic apparatus and the equatorial layer of both subfamilies follow the same evolutionary path even at differente rates and times. Lepidocyclininae include the genera Eulinderina, Polylepidina and Eulepidina, which represent a logical, gradual evolutionary development of the embryonic apparatus in the macrospheric generation, and Lepidocyclina, descending from Polylepidina, the embryonic apparatus of which does not evolve further. Helicolepidina and Nephrolepidina belong to the Helicolepidininae; Nephrolepidina is suggested to be a descent of a Helicolepidina species.
- Aruta L. (1982)
 
Late Miocene (Sahelian) marine Ostracods from Bonfornello (Palermo, Sicily)
pp. 113-132
In this paper a marine ostracods fauna obtained from the Sahelian (late Miocene) marls outcropping near Bonfornello (Palermo) is described. Fifteen species out of the 60 species identified are news: Buntonia rarepunctata n. sp., Callistocythere aspera n. sp., C. joachinoi n. sp., C. producta n. sp., Cytherella levipunctata n. sp., Cytheretta ebraica n. sp., Eucytherura russoi n. sp., Keijella lucida n. sp., K. ruggierii
n. sp., Leptocythere elliptica n. sp., L. omnireticulata n. sp., Olimfalunia ruggierii n. sp., Semicytherura gibbera n. sp., S. himerensis n. sp., Xestoleberis retropunctata n. sp.
- Aruta L. & Ruggieri G. (1982)
 
Morphologic anomalies in two ostracods from the Miocene and the Lower Pleistocene
pp. 133-135
The note deals with two anomalous specimens of ostracoda, respectively belonging to Ruggieria tetraptera (from the Miocene of Sicily) and Semicytherura acuta (from the Lower Pleistocene of Sicily). Both specimens show the distal extremity of lateroventral ala affected by a strange inflation of still unknown origin.
Issues 2-3
Published in April 1984
- Abed M.M. & Metwally M.H. (1982)
 
Some Pectinids from the Egyptian Miocene deposits near the Mediterranean shore
pp. 145-152
The presence of the shallow marine Pectinidae in an excellent state of preservation is a notable feature in the Egyptian Miocene deposits. Abundant specimens of these species were collected from the northern part of the Western Desert of Egypt, very near to the Mediterranean Sea shore.
These species are paleontologically studied and compared with those of Southern Europe.
- Ahmad F. (1982)
 
The Myth of Oceanic Tethys
pp. 153-168
Presently available evidence on the distribution of flora and fauna, the latter including vertebrates, insects and fresh-water forms, indicates that Gondwanaland and the northern continents, particularly Angaraland and Cathaysia, were never separated by an oceanic deep, as often envisaged in the past. Nor was the Tethys, sensu stricto, of geosynclinal character.
Instead, it was an epicontinental sea, transgressing and regressing frequently, covering the area from northern India to southern Siberia, and from the present western Pacific coastal area to, perhaps Italy, in its former position besides Spain. It, apparently, continued into the Appalachian Geosyncline, and through it extended from eastern to western Panthalassa. It was, thus, a truly intra-Pangaean sea. On the other hand, it continued into the Yunnan-Malay Geosyncline, and perhaps with a small gap, into the Tasman, Samfrau, and the Cordilleran (Andean) geosynclines. It might, then have provided a link between the two ends of a vast hemi-elleptical geosyncline. Simultaneously, the Cordilleran-Nevadan-Laramide geosynclines existed along western North America, and with the hemi-elleptical geosyncline, described above, formed a sigma (2) like figure. In addition, there were the Cherskyi, the Mongolian and other geosynclines. Palaeozoic Pangaea, thus abounded in them, and along with the seas besides them, a vast area of Pangaea must have been covered by sea-water.
The floral differences between Gondwanaland and Laurasia in the Permian, on which much stress was laid in the past, were obviously, climate-controlled, and were not the evidence for an oceanic separation.
It is also probable that a land bridge connected the Indian shield with the Russian shield in the region west of Pamir, but was, on occasions, submerged. Thus, an oceanic Tethys, appearing on most Pangaean assemblies and requiring collision and subduction in the Himalayan region is a myth, and accordingly the reconstructions are invalid. Since this oceanic wedge disappears when Pangaea is assembled on a globe of a smaller diameter, we may have to accept the concept of expanding Earth.
Also there is no justification for the suggested northward drift of India, as envisaged on palaeomagnetic data. Instead, it appears that polar-wandering, sensu stricto, was responsible for this anomaly, for as the South Pole migrated to its present location, India appeared to have migrated northward. Absence of relevant data from Africa and South America precludes confirmation of the evidence from India. This large north-ward drift of India supported plate-tectonic interpretations, and consequently, received wide and prompt acceptance from its proponents.
In the Himalayan-Tibetan region, on the contrary, although 4 very thick stratigraphic succession accumulated from at least the Cambrian through Cretaceous, and may be later, almost none of it is geosynclinal in character. Deep seismic sounding in the Pamir region has convincingly demonstrated that all the faults in the area are high-angled and some even reached into the mantle. The so-called Indus Suture Zone is, in fact, a rift valley, and its eruptions might have produced some of the rocks classified as ophiolites. Numerous rift valleys and normal faults exist on the Tibetan plateau and unequivocally bespeak of tension all over the area, and not of compression, that one would expect from a subduction/collision zone.
Significant also is the occurrence of Gigantopteris flora, characteristic of the tropical parts of Cathaysia, in several areas of North America. It is inexplicable unless the Pacific itself was of a much smaller width, and permitted direct migration, for northeast Siberia was having a glacial climate in the Permian and this tropical flora could not migrate across it.
- Alméras Y. & Elmi S. (1982)
 
Variations of ammonite and brachiopod-populations in relation with bathymetric changes during the Lower and Middle Jurassic in the Western Mediterranean
pp. 169-188
Ammonite communities are often considered as pelagic indicators, whereas brachiopods should be bound more to neritic conditions. The study of carbonate-platforms and of their tectonic control, the use of paleotectonic and sedimentologic data allow a better approach of the population-dynamics.
The palaeobiogeography of brachiopods depends, but not exclusively, on the bathymetry which is mainly tectonically controlled. Thus, during the Lotharingian-Carixian, the large extension of the western mediterranean carbonate-platforms has induced infratidal, and even, tidal and confined environments which prevent the dispersion of the brachiopods and their mixing. In these conditions, an isolation occurs between the populations living in different sub-basins in process of differentiation: Hesperithyris fauna from Morocco and Italia (Southern Alps, Central Apennines, Calabria); T. davidsoni – Cuersithyris fauna from Portugal, Spain (Balearics, Iberic Cordillera) and France (Pyrenees, Provence); faunas from the Southern Alps (Aulacothyris furlana, Zeilleria hierlatzica…) are ranging within the Betic domain.
But, from the Domerian until the Bathonian, a relative homogeneisation of brachiopod-faunas occurs inside the tethyan domain and, sometimes, in Middle Europa. It is consecutive to the sinking of the carbonate-platforms. These events allow the migrations along emerged lands on the continental shelf which afford good fixation substrates and where existed abounding food supplies (high fertility).
Concerning the ammonites, the beginning of the dislocation (Lotharingian-Carixian) is coeval with the first exchanges between tethyan and european domains as testified by the northward displacement of Prodactylioceras and Harpoceratinids. These relations remain exceptional. Indeed, the tilting-blocks tectonics favourish the multiplication of ecological niches occupied by founding faunas which could sustained strongly unfavourable conditions.
At the end of the dislocation-process (Domerian), a general competition arises between mixed faunas (Amaltheids, Harpoceratinids). During the Toarcian, the ecological niches are restricted to confined bottoms or to shallow water zones. An exemple is given by dwarf faunas with atypical variability known in certain narrow subsiding furrows (Valdorbia).
- Angelucci A., Boni C.F., Bono P., Carbone F., Ciancetti G., Civitelli G., D’Alessandro L., Funiciello R., La Monica G.B., Lombardi S., Lupia Palmieri E., Mariotti G., Matteucci R. & Toro B. (1982)
 
Ghubbet Entatu bight in the Dahlak Archipelago (Red Sea): a case of carbonate sedimentation
pp. 189-200
Ghubbet Entatu is a shallow bight at the northwestern end of the Dahlak Archipelago in Southern Red Sea. This bight is one of the many hollows, ranging in depth from 30 m to more than 150 m, probably to be connected with salt tectonics due to a thick evaporite sequence underlying carbonate rocks. Salt tectonics is superimposed to the regional one, and it controls the morphological assessment and the sediment characteristics of the whole archipelago.
In the Ghubbet Entatu bight, ellipsoidal in shape and with a maximum lenght of 15 km about, the 30 m deep central hollow is interested by lime mud sedimentation, whereas along the bight borders and in the small bays like Khor Melill and Khor Und Abi, skeletal sediments without mud prevail. Sediment pattern seems to be linked to the tide and the central hollow acts as a trap for the finest sedimentary particles.
The micrite is characterized by abundant pelecypods (Corbula prevails) with young and well preserved shells, foraminifera (the most frequent is Challengerella bradyi) and pteropods (essentially Creseis acicula). In coarser sediments the faunal assemblage with Arcidae, Plicatula, Miliolidae and Textulariidae is less rich.
- Angelucci A., Carbone F. & Matteucci R. (1982)
 
The Ilisi fringing reef in the Bagiuni Islands (Southern Somalia)
pp. 201-210
In the fringing reef of Ilisi Island, from sea landwards, the following facies can be recognized: a) sandy plain with isolated bathymetric highs (depth 8-12 m); b) high steepness fore-reef slope densely covered by soft corals (Sarcophyton) and branched Poritids; c) reef rim covered by extensive masses of branched Porites; d) reef-flat characterized by little covering of corals and wide-spreading of biogenic pieces coarse gravel size; e) isolated patch-reefs in the very thick thriving plain; f) upper subtidal-intertidal zone.
Well developed Thalassodendron grasslands give an important contribution to sediment production; most part of the carbonatic material derives from the mechanical destruction of incrusting carbonate Red Algae growing round the stems: these muffs support flourishing population of articulate corallinaceans.
- Bernasconi M.P. & Robba E. (1982)
 
The Thecosomatous Pteropods: a contribution toward the Cenozoic Tethyan paleobiogeography
pp. 211-222
The Tethyan seaway seems to have had a rather low efficiency on the migration of Pteropods from Atlantic-Mediterranean toward Indo-Pacific and vice versa. The faunal interchanges between Caribbean-Mediterranean-Paratethys were active by the Oligocene and extended to Asia Minor as well during Middle Miocene; migration seems to have occurred from West toward East. Pteropods have been especially confined to the Atlantic-Mediterranean area until the entire Miocene at least; their Recent wide dispersal and ranges of species came to a definitive settlement during the Pleistocene.
- Bizzarrini F. & Braga G. (1982)
 
The Triassic Bryozoa of the Western Tethyan basin
pp. 223-234
The faunal assemblages of the Lower-Middle Triassic belong exclusively to palaeozoic surviving forms; in sum, there are 5 genera of Trepostomata and 2 of Cryptostomata.
In the Western Tethyan basin these occupy the reef environment (fam. Trematoporidae) and the shallow coastal sea (gen. Pseudobatostomella).
Cerioporinae, which joined and/or replaced Trematoporidae in the reef facies, occurred during the Ladinian-Carnian transitional stage in the above-mentioned basin, and later became widespread.
Tubuloporinae also spread during the Carnian in reef environment as encrusting Porifera and Corals.
In the epicontinental shallow waters of Western Tethys and in other Triassic seas, only surviving palaeozoic faunas are known (almost exclusively Trepostomata).
In sum, during the whole of the Triassic, 5 familiae and 10 genera of Trepostomata, 2 familiae and 2 genera of Cryptostomata and 2 familiae and 6 genera of Cyclostomata are reported; some Tubuloporina forms currently being studied by the Authors must be added.
The Authors also point out that up till now Triassic Cerioporinae have been found exclusively in the reef facies of the Western Tethyan basin.
The beginning and spread of these forms may have taken place during the Middle-Upper Triassic in the reef environment of the above-mentioned basin.
The group from which the Cerioporinae originated is doubtful, although Boardman (in: Recent and fossil Bryozoa, 1981) believes that Cerioporinae may descend from palaeozoic Trepostomata.
- Boccaletti M. (1982)
 
The Perimediterranean mountain chains in the framework of Tethys evolution
pp. 235-242
Two major stages are distinguished in the geodynamic evolution of the peri-mediterranean chains: 1) a first oceanic stage, ending in Cretaceous-Eocene with the complete closure of the Mesozoic oceanic basins between the Eurasia and the Afro-Arabian block and 2) a following continental stage, responsible of the Neogene-Quaternary deformations.
Concerning the first stage, the hypotheses about the number of original Mesozoic oceanic branches in the eastern Mediterranean region and about their relationship with the Paleotethys, are discussed. A model for the formation of the Ligurian-Piedmont oceanic basin is also indicated.
Concerning the second stage, a model of ensialic evolution, which induces and guides the continental lithosphere subductions, is proposed.
- Maxamed C.M. & Carush M.C. (1982)
 
The Indo-Mediterranean characters of the Somali shallow marine benthic faunas from Jurassic up to Oligocene
pp. 243-254
Examination of the paleontological literature and direct sampling of fossils in the stratigraphic series of Somalia show that the characters of the shallow marine benthic faunas (macroforaminifera, brachiopoda, bivalvia, gastropoda, echinida) are of Indo-Mediterranean type from the Jurassic (beginning of the paleontological record in Somalia) up to Oligocene.
Affinities have been of Indian and East African type since the Miocene, but with few exceptions no more direct relationships with coeval Mediterranean faunas can be shown.
Interruption of marine continuity with the former western part of the Tethys explains the fact better than climatic reasons.
On the contrary, climate seems to be the main cause for the reduction, step by step, of the extension areas of these faunas in Northwestern Europe during the Mesozoic.
- Chonglakmani C. (1982)
 
The Mesozoic Marine Faunas of Thailand and their Paleogeographic Implications
pp. 255-266
The Mesozoic sediments are distributed extensively in Thailand. They are mainly marine (Mae Moei and Lampang Groups) in the north, west and south, but are non-marine (Khorat Group) in the northeast. The marine sequences were accumulated in three sedimentary basins, the Mae Sariang-Kanchanaburi Basin in the west and northwest comprising the Mae Moei Group (? Lower Triassic-Upper Jurassic), the Lampang Basin in the central north represented by the Triassic Lampang Group (Upper Griesbachian-Lower Norian), and the Songkhla Basin (Na Thawi Formation – Upper Triassic) in the south.
The Mae Moei Group can be divided into upper and lower units. The Lower Mae Moei Group consists of three formations, viz., the basal unnamed redbed, the middle Mae Sariang Formation, and the top Kamawkala Limestone. A shallow marine fauna consisting of bivalves, ammonoids, brachiopods and other invertebrates ranging in age from Norian to Aalenian was recorded from the Kamawkala Limestone, while a deeper offsbore Halobia fauna (Middle-Upper Triassic) characterizes the predominantly clastic Mae Sariang Formation. The Upper Mae Moei Group consists of shales and sandstones with intercalations of limestones and contains ammonite faunas of Middle-Upper Jurassic age.
The revised classification of the Lampang Group in ascending order is as follows: Phra That, Doi Chang, Hong Hoi, and Doi Long Formations. The Phra That Formation, consisting of tuffaceous shales and sandstones with intercalations of limestones, contains Claraia–Ophiceras (Upper Griesbachian), Costatoria and Hollandites–Leiophyllites (Lower Anisian) faunas. The Doi Chang limestone is represented by the Hollandites–Balatonites fauna (Upper Anisian). The predominantly clastic sequence of the Hong Hoi Formation contains Daonella (Ladinian-Karnian), Halobia (Karnian) and Indopecten (Lower Norian) faunas. The ecologic interpretation of these faunas is discussed.
From the analysis of the marine Mesozoic invertebrate faunas, it suggests that during the Mesozoic Thailand was not part of Gondwanaland. Paleogeographically, Thailand was situated at the eastern part of the Tethys. It consists of two continental blocks, the Shan-Thai and the Indosinian, which have been joined together since Upper Triassic times. The Mesozoic marine sediments were deposited on both margins of the Shan-Thai block. The rock sequence of the Lampang Basin was folded and uplifted during the Middle Norian Indosinian Orogeny (Upper Triassic), while that of the Mae Sariang-Kanchanaburi Basin was affected by the Late Jurassic-Early Cretaceous Young Cimmerian Orogeny which ultimately consolidated the whole country into a single stable landmass.
- Farinacci A. & Köylüoglu M. (1982)
 
Evolution of the Jurassic-Cretaceous Taurus shelf (Southern Turkey)
pp. 267-276
Carbonate sequences of the Taurus moutains are the result of the sedimentation in a wide shallow marginal sea. Due to the Tethys opening in the Late Triassic, sedimentation was strongly influenced by tectonics and sea level variations.
Both frequent short subaerial exposures and long emergences of the shelf are recognized through facies analysis. Oolitic shoals and barrier rim environments of the Lower Jurassic developed into Upper Jurassic and Lower Cretaceous restricted lagoons.
Growth of Lower Turonian Rudist reefs was widespread on the shelf, but these were drowned during the Upper Cretaceous general transgression and particularly during Campanian-Maastrichtian time.
- Franco F. (1982)
 
Late Paleogene and Neogene Indo-Mediterranean molluscs
pp. 277-282
The Mediterranean Sea ceased to have direct marine connection with the Indian Ocean at the beginning of the Neogene. The Oligocene mollusc faunas of the two marine basins have many species in common. During the Neogene common mollusc species are found at various geologic levels. This phenomenon is better explained by temporary, repeated, marine connections during the Neogene than by the survival of the same species in the two seas after their separation.
- Hartenberger J.L. (1982)
 
Vertebrate faunal exchanges between Indian subcontinent and Central Asia in early Tertiary times
pp. 283-288
Early Paleogene rodents of Asia have been reviewed. On the basis of their evolutionary history and additional indications given by other groups of mammals, paleobiogeographic conclusions are drawn up. In middle Eocene times Indian subcontinent has a particular fauna which can be considered endemic in regard of Central Asiatic one. It is suggested that ancestors of these forms were widespread all over India and Central Asia at the beginning of the Eocene; a biogeographic barrier segregated Indian subcontinent faunas from those of Central Asia soon after. This should be a consequence of a climatic zonation as well as a physical barrier. New collectings of Vertebrates in the Paleocene of India suggest that by this time Indian faunas had Laurasiatic affinities. No indication of African affinities can be recorded in Indian terrestrial vertebrates of early Paleogene age.
- Khawlie M., Mroueh M., Ghalayni I. & Hamdan W. (1982)
 
Paleo-environmental conditions of deposition of the Jurassic sequences in Kfarhounah Area (South Lebanon)
pp. 289-296
The Middle and Upper Jurassic limestone sequence in southern central Lebanon represents carbonate units deposited over an open marine shelf. The environments of deposition, entirely under low to moderate energy conditions, consist of a general slope over relatively shallow shelf-marginal flats with local shoals. Petrographic analysis reveals five distinct microfacies that are cyclic, as they recur in each unit. They are characterized by: oncolites with pellets, pelecypods-crinoids, and sponges-pelecypods. All show minor other components, and minimal detrital influx.
Geochemical facies analysis, on organic matter, insoluble residue, Fe, Cu, Mo, Ni, and Pb confirms the petrographic results.
The carbonate units generally deposited in normal marine salinities and open conditions.
- Kotaka T. (1982)
 
Geologic History of Japanese Turritellid Fauna in Japan and adjacent Regions
pp. 297-302
Biostratigraphy of the Japanese turritellid fauna is discussed in relation to their origin, migration and evolution in and around the Japanese Islands and the adjacent regions in Cenozoic time.
- Martinell J. (1982)
 
Pliocenic shallow marine environments from NE Spain
pp. 303-310
In the marine Pliocene of Empordà (Catalunya, Spain), fourteen faunistic associations were distinguished, all of them characteristic of the shallow environments. Ten of these, very probably synchronous, are found in the yellow sands that form the upper Pliocene levels of this area. The other four associations are found in the lower blue clays. The general characteristics of these associations are described, naming them in the basis to the most representative taxons.
- McKenzie K.G. (1982)
 
Palaeozoic – Cenozoic Ostracoda of Tethys
pp. 311-326
Tethys was a warm Palaeozoic-Cenozoic sublatitudinal ocean/sea which ranged from the Americas eastwards to Australasia. There are now two widely divergent opinions on its nature. The adherents of Plate Tectonics claim that, at the development of Pangaea in the Permian, Tethys was wide and wedge-shaped, opening eastwards; that it gradually closed as Gondwanaland broke up, and disrupted finally in the Neogene. The other group visualises Tethys as analogous to the modern Mediterranean in its shape but not as narrow, and of vastly greater extent, more or less continuous from Central America to Australia for most of its history until it terminated finally in the Neogene.
Since Ostracoda range worldwide from Cambrian-Recent they prove useful in assessing these opposing viewpoints. Bradoriida, Leperditicopida, Entomozoacea, Eridostraca and Podocopida are taken as exemplar groups.
The critical faunas are deepwater ones. There are few known deepwater assemblages from Tethys until the Jurassic; and following the Cretaceous the best studied deepwater taxa are those of Europe and the DSDP cores. But shallow water assemblages characterise Tethys throughout its history. Faunal provincialism becomes progressively more marked from the Late Mesozoic onwards.
On the evidence, Tethys may have been an elongate, relatively shallow, thermospheric, sublatitudinal, intercontinental sea during the later Palaeozoic; became deeper in the Mesozoic, and retained oceanic characteristics throughout the Palaeogene. It disrupted in the Neogene.