Maria Cristina Perri

PROTOGNATHODUS (CONODONTA) AND ITS POTENTIAL AS A TOOL FOR DEFINING THE DEVONIAN/CARBONIFEROUS BOUNDARY

The current definition of the Devonian/Carboniferous boundary is the first occurrence of the conodont Siphonodella sulcata . Due to difficulties in identification of the early siphonodellids, such as S. praesulcata and S. sulcata , investigation of Protognathodus which enters in the latest Devonian and extends into the Mississippian, was undertaken to determine use as a better indicator of the base of the Carboniferous. During the D/C boundary interval, Protognathus is represented by four species: Pr. meischneri , Pr. collinsoni , Pr. kockeli and Pr. kuehni. Although Pr. kockeli can be abundant in boundary interval sections, none of the four Protognathodus species has a high potential as a tool for redefining the D/C boundary, based on regional variation in first occurrence data, restricted stratigraphic ranges and global distribution, poorly understood facies occurrences, as well as general rarity of the taxa.

Millennial Physical Events and the End-Permian Mass Mortality in the Western Palaeotethys: Timing and Primary Causes

This chapter focuses on the nature and pattern of four transgressive–regressive depositional cycles (C1–C4) across the Permian–Triassic Boundary (PTB) in the Dolomites, on their timing and on the possible causal relationships with four mass-mortality events (E0–E3), which, considered together, constitute the end-Permian extinction event in the western Palaeotethys. The duration of the investigated interval is ca. 200 ky; the duration of each cycle ranged from less than 20 ky to ca. 100 ky; and the magnitude of the sea level changes ranged from 5 to 15 m. Each mass-mortality event affecting the shallow marine environments of the western Palaeotethys corresponds with a regressive phase lasting a few millennia. The oldest mortality event (E0) at the top of Cycle 1 (i.e., the top of the Ostracod Unit) in the Southern Alps is aligned with the regressive Bed 24e of the Meishan D section in the eastern Palaeotethys; it is usually considered the actual end-Permian extinction event. The same cooling/fall-stand has been identified in various sites along the shallow-marine Gondwana margin. In the Southern Alps, E0 is mostly masked by stressed conditions typical of the regional carbonate tidal flat. During the following transgression and high-stand periods of Cycle 2 (i.e., Bulla Member), the shallow marine environment became re-populated by ca. 200 species referred to ca. 30 genera. At the top of Cycle 2, the sea level fell 10 m or less in a few millennia; it started the most devastating mass-mortality event (E1) in the Southern Alps. This mortality event lasted less than 20 millennia; it continued briefly during the trangressive phase of the following Cycle 3—which brackets the Bellerophon-Werfen formational boundary (BWB). This interval, aligned with Beds 26–27a at Meishan in the eastern Palaeotethys, was deposited in a deeper and distal environment. About 90% of the marine skeletal biomass disappeared at the end of E1. The acme of mortality event, E1, corresponded with a submarine chemical-corrosion event, followed locally by subaerial exposure and pedogenesis. The mass-mortality event on land slightly predates—or is nearly coeval—with the mass-mortality event in shallow marine environments. The intensity of submarine corrosion became almost imperceptible at the foreshore–offshore boundary. The sea level rose ca. 15 m during Cycle 3 when the shallow marine environment, mostly over-saturated in carbonate but punctuated by short periods of vadose or submarine dissolution, transgressed rapidly more than 40 km inland over the corroded bedrock, depositing oolite shoals and microbialite. The subsequent mortality events E2 and E3 are obviously of less intensity. E2, ca. 20 ky after E1, corresponds to a regressive interval associated with the first appearance of Hindeodus parvus (i.e., the Permian–Triassic Boundary). It seems to be the acme of colonisation of the shallow sea floor by cyanobacteria (stromatolites). E3, ca. 10 ky after the Permian–Triassic Boundary, corresponds to the last occurrence of Permian-type red algae in the Dolomites area. Whereas the end of E3 is gradual in the shoreface, it appears to have been abrupt in the lower foreshore, probably because of general conditions of less-ventilated and suboxic conditions. We hypothesise that a few local palaeo-environmental factors (e.g., distance of stressing factors from the source area, the pattern of atmospheric and marine palaeocurrents, and reduction of the shallow coastal area due to retreat of the coastline) concurred to modulate the intensity and duration of mortality events in space and time. Data suggest that increased warming was of primary importance in controlling the mortality tail but doesn’t allow us to confirm or deny other local or general concurrent causes, such as up-welling of anoxic oceanic waters from the Palaeotethys. We interpret the cause of the mass-mortality events in the Dolomites area as having been a composite “top-down” mechanism with acid-rain events devastating the Permian-type life on continental and, subsequently, in shallow marine environments during millennial periods of cooling and regression of the Bellerophon sea. The ultimate causal factor was, very probably, large atmospheric perturbations connected with volcanism. Most of the sparse surviving biota disappeared immediately after the beginning of the following transgression―because of rapid global warming produced by greenhouse conditions, with only minor, repeated, episodes of acid rains. These stressed conditions contributed to inhibiting recovery of the long and efficient shallow-marine food chain. Because the magnitude of mass-mortality event E0 in the Dolomites and in much of the Gondwana margin is appreciably lower than the coeval one in Meishan, the first may have acted as refugia. Mass-mortality event E1 affected the shallow-marine western Palaeotethys for only a few millennia after E0. In the eastern Palaeotethys, coeval Beds 26–27a of Meishan were deposited from lower foreshore to marine shelf, lacking any clear record of anoxic conditions. It is the same for the coeval short-term parasequences in many sites along the Gondwana margin. We interpret the different magnitude of extinction on the shelves as due to different levels of temperature and excessive carbon dioxide (pCO2) in the seawater. The rapid demise of taxa (occurring concordantly with the diachronous major mortality events) caused local severing of food chains, mostly of small suspension feeders, resulting in the “Lilliput” faunas (sensu Twitchett 2005) of event E2 in the Dolomites. This aligns with Beds 27c–d at Meishan―these beds were deposited in the lower foreshore and marine shelf environments under suboxic to dysoxic bottom conditions. It seems unlikely that the disappearance of red algae in the western Palaeotethys was connected with dysoxic conditions; increased temperature seems a more likely factor. Doubtless a medley of different mechanisms, including rapid fluctuations in marine salinity, operated variously as regards time and space and produced the end-Permian extinction―occurring over a time span of less than 100 ky.

Famennian Chondrichthyan Microremains from Morocco and Sardinia

Abstract New material from the Famennian of Morocco in the southern Maider comprises chondrichthyan teeth (Thrinacodus, Cobelodus, Denaea, Stethacanthus), actinopterygian remains (scales, teeth and hemilepidotrichium) and one acanthodian scale. The absence of crushing teeth suggests deeper water environments for the Maider Basin than the Tafilalt Basin. Vertebrate microremains from the Famennian of Sardinia, including Siamodus and Jalodus teeth, are illustrated and described. Ichthyofaunal relationships of the North Gondwanan platform during the Famennian are examined.