Neoproterozoic-early Cambrian successions in Iberia are reexamined. A gradual transition across the Neoproterozoic-Cambrian boundary is present in Central Iberia, whereas in the Cantabrian region and the Iberian Chains Lower Cambrian arenaceous successions rest with profound angular unconformity on Neoproterozoic turbidites. In Central Iberia, the Neoproterozoic sedimentary succession is referred to the informal Domo Extremeño group, representing mostly basinal facies, and the overlying Rio Huso group consisting of slope deposits and proximal turbidites that grade into shallower marine deposits. The latter is inferred to represent distal slope to outer platform depositional conditions and contains widespread carbonate olistostromic units. The position of the Precambrian-Cambrian boundary is within the Pusa shale of the Rio Huso group and can be correlated at the regional level by the occurrence of trace fossils, acritarchs, and in particular the abundant shelly metazoan Cloudina. The succession also yielded megascopic carbonaceous fossils, such as vendotaenids and Beltanelioides? sp. ind., and Sabellidites. Contrary to former interpretations assuming transport of older platform carbonates from the Ibor region into ‘younger’ olistostromic beds of the Rio Huso group, we interpret sedimentary and fossil evidence to suggest that shallower platform deposits of the informal Ibor group were penecontemporaneously incorporated in the olistostromic lower part of the Rio Huso group. Hence, the olistostromes are not believed to mark a major erosive unconformity. Based on the ichnofossil record and recent U-Pb age determinations, we argue that a proposed disconformity between Lower and Upper ‘Alcudian’ strata is neither regional nor does it mark a significant hiatus. Neoproterozoic-early Cambrian deposition in Central Iberia can be accommodated in a model that implies a generalized stretching of the crust during an extensional event which closely followed the Cadomian phase of the Pan-African Orogeny and which eventually could have included transcurrent components. An extensional phase with transcurrent components during the deposition of the Ibor and lower Rio Huso groups is regarded as a probable cause of widespread ponding resulting in the juxtaposition of platform and basinal successions, eventually leading to anoxic conditions in Pusa shale deposition times. A possible cause for repeated collapse events developing olistostromes and intra-sequential folding could be sought in this tectonic context.

Morphological and reproductive features and cell wall ultrastructure and biochemistry of Proterozoic acritarchs are used to determine their affinity to modern algae. The first appearance datum of these microbiota is traced to infer a minimum age of the divergence of the algal classes to which they may belong. The chronological appearance of microfossils that represent phycoma-like and zygotic cysts and vegetative cells and ⁄ or aplanospores, respectively, interpreted as prasinophyceaen and chlorophyceaen microalgae is related to the Viridiplantae phylogeny. An inferred minimum age of the Chlorophyte origin is before c. 1800 Ma, the Prasinophyceae at c. 1650 Ma and the Chlorophyceae at c. 1450 Ma. These divergence times differ from molecular clock estimates, and the palaeontological evidence suggests that they are older.

No abstract

No abstract

New information on acritarchs from the Duolbagáisá Formation, Digermulen Peninsula, Arctic Norway, enable recognition of the three Cambrian Series 2 acritarch-based zones: the Skiagia ornata–Fimbriaglomerella membranacea, Heliosphaeridium dissimilare–Skiagia ciliosa and Volkovia dentifera–Liepaina plana Assemblage zones. Acritarchs of the Skiagia ornata–Fimbriaglomerella membranacea Zone (Cambrian Stage 3) appear near the base of the unit, close to an undetermined trilobite. In the Upper Member of the Duolbagáisá Formation, in levels with Kjerulfia n. sp. and Elliptocephala n. sp., appears an assemblage with abundant Skiagia ciliosa, indicative of the Heliosphaeridium dissimilare–Skiagia ciliosa Zone. A few metres higher appear Liepaina plana, Heliosphaeridium notatum and Retisphaeridium dichamerum, which indicate the Volkovia dentifera–Liepaina plana Zone (Cambrian Stage 4). The transition between the Duolbagáisá Formation and the overlying Kistedalen Formation is marked by the appearance of Comasphaeridium longispinosum, Multiplicisphaeridium llynense and Eliasum llaniscum, diagnostic of the Miaolingian Series. This coincides with the disappearance of Skiagia; occurrences of Skiagia in Miaolingian strata consist of reworked material related to the Hawke Bay regression at the Cambrian Stage 4–Wuliuan transition. The absence of Skiagia in higher levels of the Duolbagáisá Formation and Kistedalen Formation suggests that no unconformity formed during the Hawke Bay regression in this area. The chronostratigraphical significance of the Skiagia ornata–Fimbriaglomerella membranacea, Heliosphaeridium dissimilare–Skiagia ciliosa and Volkovia dentifera–Liepaina plana zones is critically analysed. Correlation of the Duolbagáisá Formation with peri-Gondwanan terrains of Avalonia and Iberia is established. The Digermulen Peninsula has great potential as a reference section for establishing a Cambrian chronostratigraphy based on acritarchs.

We report on new occurrences of the late Ediacaran problematicum Palaeopascichnus (Protista?) from the Stáhpogieddi Formation, Arctic Norway. The stratigraphically lowest occurrences are in beds transitional between the Lillevannet and Indreelva members: the highest in the second cycle of the Manndrapselva Member, stratigraphically close to the lowest occurrences of Cambrian-type trace fossils. This establishes a long stratigraphical range of Palaeopascichnus on the Digermulen Peninsula, as has been previously documented from Newfoundland, South Australia, and elsewhere in Baltica. The age range of Palaeopascichnus in Avalonia and Baltica is from ∼565 to 541 Ma. Since the transition from the Mortensnes Formation to the Stáhpogieddi Formation is without a major break in sedimentation, this supports the inference that the underlying glacigenic Mortensnes Formation is ca. 580 Ma, and therefore Gaskiers-equivalent, or younger.

Acritarchs are reported from basal Cambrian rock units inthe Cantabrian region of northern Spain that are known to contain archaeocyathan and trilobite faunas. Biostratigraphic correlation of the Iberian sequences with other regions has been hampered by the strong provincialism of these faunas. However, this report of evidently cosmopolitan acritarch taxaestablishes the time equivalence of early Cambrian trilobite faunas from Iberia, Baltoscandia and the East European Platform (EEP). Our data suggest that the detrital deposition of the Lower Cambrian Herreria Formation embraces at least three (and possibly four) Lower Cambrian acritarch zones previously identified in the EEP, eastern Siberia, Baltoscandia, Scotland, Greenland, Svalbard and western North America. The early Cambrian transgression in northern Spain was probably initiated in Talsy times (Schmidtiellus mickwitzi trilobite Zone in Baltoscandia and the EEP), in part corresponding to the Dokidocyathus regularis archaeocyathian Zone of the Middle Tommotian in Siberia.

Diverse and well-preserved acritarchs are reported from the type section of the Cambrian Hanford Brook Formation at Hanford Brook, southern New Brunswick. This section fills an important gap in acritarch studies by providing the first detailed picture of changing acritarch associations close to the traditional lower–middle Cambrian boundary in Avalonia. Acritarchs from the St Martins Member, at the base of the succession, include Skiagia ciliosa, Heliosphaeridium notatum, H. longum and Liepaina plana and suggest attribution to Cambrian Stage 4. Acritarchs from the Somerset Street Member, in the middle of the formation, include Eliasum llaniscum and Comasphaeridium silesiense. This information adds new biochronological context to an ash bed in the Somerset Street Member previously dated as c. 510 Ma or 508 Ma, and to the endemic trilobites from the same member, including Protolenus elegans. It also places absolute ages on the basal range of stratigraphically important acritarchs. Both the acritarch assemblage and the radiometric age are consistent with a position very close to the traditional lower–middle Cambrian transition and likely within Cambrian Stage 5. Acritarchs from the Long Island Member, at the top of the succession, include additional taxa demonstrating assignment to Cambrian Stage 5. Both the Somerset Street and Long Island members probably correlate with the Morocconus notabilis Zone. The new acritarch species Retisphaeridium striatum Palacios is described. New data are presented on acritarchs from the upper part of the Hell's Mouth Formation, Wales, and correlation proposed with the Long Island Member.