Wyniki wyszukiwania - BazTech

1

Lower Toarcian organic-rich sediments from the Tuscan Succession (Northern Apennines, Italy): preliminary results

Perilli N., Rodrigues R., Veiga de Oliveira L., Catanzariti R.

Volumina Jurassica

|

2009

|

Vol. 7, no. 1

55-65

EN

For the first time is here documented the presence of Lower Toarcian black shales in the lower portion of the Calcari e marne a Posidonia (Posidonia Marls auctt.) belonging to the Tuscan Nappe. It consists of alternations of 30 cm to 5 m thick black laminated marlstone and marly claystone, with TOC values ranging from 0.43% to 2.49%. Based on calcareous nannofossils, the basal portion of the Calcari e marne a Posidonia spans the Lotharingius hauffii to Carinolithus superbus zones, and the organic-rich interval lies within the Carinolithus superbus Zone.

2

The Pliensbachian/Toarcian boundary in the Almonacid de la Cuba section (Iberian Range, Spain)

Goy A., Comas-Rengifo J., Gomez J., Gonzales J., Herrero C., Palencia A., Perilli N., Rodrigo A.

Volumina Jurassica

|

2006

|

Vol. 4, no. 1

164-166

EN

The Almonacid de la Cuba section, representative of the Pliensbachian-Toarcian transition in the Iberian Range (Fig. 1), is reviewed. It is an expanded section where no important discontinuities have been detected. Four successive assemblages of ammonites, which are characterized by the presence of Pleuroceras (BH14-CU14), Canavaria (CU16-CU32), Dactylioceras (E.) (CU35.2-CU44) and Dactylioceras (O.) (CU44-CU87), are distinguished. The Pliensbachian/Toarcian boundary is located at the base of level CU35.2 with the first record of Dactylioceras (Fig. 2). These assemblages are mainly constituted by taxa typical of the NW European Province, such as Pleuroceras, Dactylioceras (O.) and P. paltum. However, frequent Mediterranean Province taxa such as Emaciaticeras, Canavaria, Lioceratoides, Neolioceratoides, Dactylioceras (E.) and P. madagascariense, are also recorded. In the Tenuicostatum Zone, dactylioceratidae are dominating with respect to harpoceratinae. In the Mirabile Subzone, species of Dactylioceras (E.) are coexisting with P. paltum. Brachiopods show two successive assemblages. The lower one is composed generally of the Pliensbachian taxa and the upper assemblage includes more endemic taxa. Coinciding with the Early Toarcian OAE, almost all these species disappeared at the end of the Tenuicostatum Chron. Foraminiferal assemblages are rich and diversified. Calcareous hyaline taxa are dominated by suborder Lagenina, agglutinated foraminifera are scarce, the suborders Spirillinina and Miliolina are represented by few specimens and taxa, and specimens of Robertinina have been recovered throughout the whole stratigraphic interval. The main biostratigraphical foraminiferal events can be recognized and compared with other sections of the Iberian Range and with another ones of selected NW European Basins. Ostracod assemblages of the Spinatum Zone are dominated by healdiids and cytheraceans, which decrease at the base of the Tenuicostatum Zone, where the cypridaceans are better represented. In the Semicelatum Subzone, coinciding with the disappearance of the healdiids, the cytheraceans become dominants.Calcareous nannofossils assemblages are rich and well preserved. This allowed locating precisely the biochronostratigraphical position of the main markers and events and comparing them with these recorded in other basins of Western Tethys. A magnetic polarity column for the Pliensbachian/Toarcian boundary has been constructed on the basis of the polarities of the 2C Component (Fig. 2). The lower boundary of the Toarcian is located within the R2 magnetozone. A relatively large magnetozone N3 of normal polarity is located within the Tenuicostatum Zone.

3

Pliensbachian calcareous nannofossil zones vs ammonite zones along the western and northern margins of the Iberian Massif and biostratigraphical potential of nannobiohorizons

Perilli N., Veiga de Oliveira L., Comas-Rengifo M., Duarte L.

Volumina Jurassica

|

2006

|

Vol. 4, no. 1

202-203

EN

Calcareous nannofossils, one of the main components of Lower Jurassic marly/limestone alternations, were studied along the western and northern margins of the Iberian Massif. Consequently, they were used to date the lithological successions as well abiotic signals (e.g. isotope or TOC profiles). Our work focuses on the main changes of calcareous nannofossil record and the biohorizons recognized in some reference Pliensbachian sections from Basque-Cantabrian area (Spain) and Lusitanian Basin (Portugal). The remarkable changes in composition are the appearances and abundance increases of the Biscutaceae (Similiscutum) and of Watznaueriaceae (Lotharingius). The appearances of large Biscutum (B. grande and B. finchii) and of medium-sized Lotharingius species (L. sigillatus) are also clearly detectable though their occurrence is discontinuous. The other events include the appearances of Biscutum dubium, Bussonius prinsii, Biscutum novum and Crepidolithus impontus and the disappearance of Parhabdolithus robustus. The reconstructed distribution pattern of the age-significant species supports the identification and description of the nannofossil zones and subzones proposed for NW Europe. The NJ3/NJ4, NJ4/NJ5 zone boundaries are easily identified by the FO of Similiscutum cruciulus (Lower Pliensbachian) and the FO of Lotharingius hauffii (Upper Pliensbachian), respectively. The subzone boundaries should be carefully checked because the zonal markers are rare and occur discontinuously. However, the other events are helpful to correlate the biostratigraphic frames outlined for the investigated areas and to calibrate the NJ4a/NJ4b, NJ5a/NJ5b zone boundaries with respect to the ammonite zones. Based on the achieved data, the main differences between the two schemes are related to the very low abundance and discontinuous occurrence of the some species in their initial (e.g., B. grande, B. finchii) or final (e.g., P. robustus) ranges. Since for the Basque-Cantabrian area ammonite zone and subzones are well constrained, some discrepancies should be related with a discontinuous or incomplete ammonite record from the Lusitanian Basin. Nevertheless, the biostratigraphic frames proposed for both areas could improve biochronocorrelation between the Pliensbachian successions cropping out along the western and northern margin of the Iberian Massif.

4

Lower Toarcian organic-rich sediments from the Tuscan Succession (Northern Apennines, Italy)

Perilli N., Veiga de Oliveira L., Rodrigues R., Catanzariti R.

Volumina Jurassica

|

2006

|

Vol. 4, no. 1

203-204

EN

This work is aimed to improve lithostratigraphy and biostratigraphy, based on calcareous nannofossils, of the deep-marine Lower Toarcian sediments belonging to Tuscan Nappe (Northern Apennines). The sampled lower part of the Calcari e marne a Posidonia (Posidonia Marls) correlates with the Marne del Monte Serrone of the Umbria-Marche Basin, which is characterized by the presence of the Lower Toarcian black shales. The Calcari e marne a Posidonia consists of grey to greenish hemipelagic to pelagic bivalves-bearing marlstones and limestones with interbedded grey to grey dark, sometimes reddish, clayey marlstones and marly claystones. In some localities, in the lower portion of this formation is recognized a thin to medium thick organic-rich interval of black marlstones and marly claystones. The recovered calcareous nannofossil assemblages allow to assigne the basal portion of the Marne a Posidonia to the Lower Toarcian with the thin organic-rich interval comprised between the appearances of the genera Carinolithus and Discorhabdus.

5

Calcareous nannofossils biostratigraphy and oxygen isotope composition of belemnites: Pliensbachian – lowermost Toarcian of Peniche (Lusitanian Basin, Portugal)

Veiga de Oliveira L., Duarte L., Rodrigues R., Perilli N.

Volumina Jurassica

|

2006

|

Vol. 4, no. 1

219-219

EN

The Lusitanian Basin is located in the western Iberian margin, opened during the Triassic.The Lower Jurassic is particularly well represented at Peniche, which exhibits a continuous seriesof carbonate sediments, more than 450 m thick and aged between Sinemurian and Toarcian.In lithostratigraphic terms it corresponds to the Agua de Madeiros, Vale das Fontes, Lemede and CaboCarvoeiro formations. In this study, 145 m thick section (from the Jamesoni to the Levisoni ammonite zones),was analyzed in terms of calcareous nannofossils biostratigraphy and oxygen isotopes of belemnite rostra.The nannofossil biozones NJ4a, NJ4b, NJ5a (Pliensbachian; upper part of Jamesoni to Spinatumammonite zones), NJ5b (uppermost Pliensbachian - lowermost Toarcian; upper part of Spinatumto Levisoni ammonite zones) and NJ6 (lowermost Toarcian; upper part of Levisoni ammonite Zone) wereidentified based on proposed NW European schema and correlated with ammonite zones. Additionally,the secondary biostratigraphic events were registered which will be useful to refine the nannofossilsbiozonation: the first occurrences (FO) of Biscutum grande and B. finchii were found in the upper part ofthe NJ4a biozone (lower part of Margaritatus ammonite Zone); the FO of Lotharingius frodoi wasidentified at the same stratigraphical level as L. hauffii; the FO of L. sigillatus was found in the upper partof the NJ5a biozone (Spinatum Zone); the first common occurrence (FCO) of Calyculus spp. was recognizedin the NJ5b base, near the Pliensbachian/Toarcian boundary; the FO of Carinolithus spp. was identifiedwithin NJ5b biozone, correlated with the lower part of the Levisoni ammonite Zone and below the extinctionlevels of Calcivascularis jansae and B. grande which are other nannofossil secondary events.The oxygen-isotope profile of the Peniche section seems to reflect primary signals and can be usedto interpret the sea water paleotemperatures variations. In the Early Pliensbachian the temperature showsa gradual cooling trend (NJ3 and the lower part of the NJ4a; Jamesoni ammonite Zone). Afterward,there is a warm period (NJ4a and NJ4b; Jamesoni to lower part of Spinatum ammonite Zone) correlatedwith high TOC values interval (up to 15%), suggesting a relative sea level rise and concomitant high surfacewaterproductivity. In fact, the Margaritatus ammonite Zone corresponds, in the Lusitanian Basin,to 2nd-order flooding interval. In the Late Pliensbachian and Early Toarcian (NJ5a and lowermost partof NJ5b; Spinatum to Polymorphum ammonite zones), the isotopic values show slight variations.However, they suggest a small cooling trend in the upper part of Spinatum ammonite Zone and a warmtendency in the lower part of Polymorphum ammonite Zone.

6

Aalenian carbon-isotope stratigraphy: a tool for the ammonite radiolarian and nannofossil zonation calibrations in the Western Tethys

Sandoval J., Aguado R., Bartolini A., Bill M., Bruchez S., O'Dogherty L., Perilli N.

Volumina Jurassica

|

2006

|

Vol. 4, no. 1

212-213

EN

Here we report a detailed carbon-isotope stratigraphy for the Aalenian (Middle Jurassic) pelagic carbonates in the Betic Cordillera (southern Spain), which represents an ideal region to directly tie the stable carbon-isotope curves to ammonite zones and subzones, and thereby for the first time achieve an accurate chronostratigraphic calibration. For this purpose we have selected two sections (Agua Larga in the province of Granada and Cerro de Mahoma in the province of Murcia) which represent basinal deposits of the southern Iberian palaeomargin. In these sections ammonite are common and relatively wellpreserved. Biostratigraphic analyses enable the recognition of the uppermost Toarcian (Aalensis Zone), the complete Aalenian (Opalinum, Murchisonae, Bradfordensis and Concavum zones) and the lowermost Bajocian (Discites Zone). Calcareous nannofossils and radiolarians (at discrete beds of the Upper Aalenian - Lower Bajocian) are also common in these Median Subbetic hemipelagic sections. The Subbetic Aalenian is characterized by a monotonous and rhythmical alternance of marlstones and marls in continuous sedimentation throughout the analysed interval. We present a ?13C curve very detailed (bed by bed) for the uppermost Toarcian - lowermost Bajocian interval. The curve shows a relative minimum (around 1‰) in the Upper Toarcian, a weak positive shift (around 2‰) in Lower Aalenian (Comptum Subzone), a decreasing values (newly around 1‰) in the Middle Aalenian (Bradfordensis Zone), a positive peak of 2.7‰ in the Upper Aalenian (Concavum Zone and Subzone) and a new relative minimum (1.5-1.7‰) at Aalenian/Bajocian boundary. A good correlation among the isotope curve and the different biostratigraphic zonations is accurately presented. We explore the powerfulness of this well-calibrated ?13C curve as a tool for stratigraphic correlation. In this sense, the biochronostratigraphic position of the radiolarian UAzones 1-2 (mainly based on Italian sections with scarce record of ammonites, Baumgartner et al. 1995) are here redefined by means of the isotope reference curve of the Subbetic. We present the results of a biostratigraphic study of nannofossils assemblages throughout the studied interval. In addition, on the base of a semiquantitative study, we have selected the most abundant taxa (>10%) from the whole assemblage to perform a multivariate analysis (principal components): Biscutum dubium, B. intermedium, Crepidolithus crassus, Carinolithus superbus, Discorhabdus striatus, Schizosphaerella spp., Watznaueria contracta and the genus Lotharingius. This multivariate analysis reveals a strong correlation between the abundances of oligotrophic (C. crassus and Schizosphaerella spp.) and eutrophic (B. dubium and B. intermedium) taxa and the fluctuation of the C degree curve.