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Radiodonta, apex Cambrian predators such as Anomalocaris have been known from the Kinzers Formation (Cambrian Series 2, Stage 4 – Pennsylvania, USA) for nearly 100 years. Work over the last ten years, mainly on radiodont material from the Chengjiang (Cambrian Series 2, Stage 3 – Yunnan, China) and Burgess Shale (Miaolingian, Wuliuan – British Columbia, Canada), has greatly improved our knowledge of the diversity and disparity of radiodonts and their frontal appendages, including the description of new species, genera and families. Previous work identified two species of radiodonts from the Kinzers Formation: Anomalocaris pennsylvanica Resser, 1929 and Anomalocaris? cf. pennsylvanica based on isolated frontal appendage material (Briggs, 1979). A restudy of Kinzers Formation material shows that only some of the specimens can be confirmed as Anomalocaris pennsylvanica, and a number of specimens previously attributed to Anomalocaris in fact belong to other more recently discovered radiodont genera Amplectobelua and Tamisiocaris. This reinterpretation makes the Kinzers Formation the most diverse Cambrian Stage 4 Burgess Shale Type Lagerstätten in terms of number of radiodont species. This assemblage includes the youngest known Tamisiocaris and the first from outside Greenland, the only Amplectobelua from Stage 4 and the oldest from Laurentia, two specimens tentatively assigned to the recently described Chengjiang genus Laminacaris, and the endemic Anomalocaris pennsylvanica. The identification of these new radiodont taxa increases the total known diversity of the Kinzers Formation to more than ten species, and so it should now be considered a Tier 2 Lagerstätte.

High-precision U-Pb zircon ages on SE Newfoundland tuffs now bracket the Avalonian Lower–Middle Cambrian boundary. Upper Lower Cambrian Brigus Formation tuffs yield depositional ages of 507.91 ± 0.07 Ma (Callavia broeggeri Zone) and 507.67 ± 0.08 Ma and 507.21 ± 0.13 Ma (Morocconus-Condylopyge eli Assemblage interval). Lower Middle Cambrian Chamberlain’s Brook Formation tuffs have depositional ages of 506.34 ± 0.21 Ma (Kiskinella cristata Zone) and 506.25 ± 0.07 Ma (Eccaparadoxides bennetti Zone). The composite unconformity separating the Brigus and Chamberlain’s Brook formations is constrained between these ages. An Avalonian Lower–Middle Cambrian boundary between 507.2 ± 0.1 and 506.3 ± 0.2 Ma is consistent with maximum depositional age constraints from southwest Laurentia, which indicate an age for the base of the Miaolingian Series, as locally interpreted, of ≤ 506.6 ± 0.3 Ma. The Miaolingian Series’ base is interpreted as correlative within ≤ 0.3 ± 0.3 Ma between Cambrian palaeocontinents, although its exact synchrony is questionable due to taxonomic problems with a possible Oryctocephalus indicus-plexus, invariable dysoxic lithofacies control of O. indicus and diachronous occurrence of O. indicus in temporally distinct δ 13C chemozones in South China and SW Laurentia. The lowest occurrence of O. indicus assemblages is linked to onlap (epeirogenic or eustatic) of dysoxic facies. A united Avalonia is shown by late Early Cambrian volcanics in SW New Brunswick; Cape Breton Island; SE Newfoundland; and the Wrekin area, England. The new U-Pb ages revise Avalonian geological evolution as they show rapid epeirogenic changes through depositional sequences 4a–6.

New U–Pb radioisotopic ages on early Cambrian volcanic zircons condition a high-resolution Bayesian age model that constrains the first occurrences and zonations of West Gondwanan archaeocyaths and trilobites in southern Morocco. The oldest archaeocyaths in the Tiout Member of the Igoudine Formation (519.71 + 0.26/− 0.35 Ma) are c. 6 Ma younger than the oldest Siberian archaeocyaths. The oldest Moroccan trilobite fragments, from the lower member of the Igoudine, are constrained to 519.95 + 0.43/− 0.40 Ma. The succeeding Issendalenian Stage (i.e. Hupetina antique – Eofallotaspis tioutensis – Fallotaspis plana – Choubertella – Daguinaspis trilobite zones) spans c. 1.5 Ma (519.78 + 0.26/− 0.37 Ma to 518.43 + 0.25/− 0.69 Ma). Identifiable Moroccan fallotaspidids and bigotinids, among Earth’s oldest trilobites, occur above a positive δ13C excursion dated with our age model at 520.27 + 0.59/− 0.57 Ma, and correlated with the IV excursion peak within the lower range of Siberian Atdabanian Stage trilobites (Repinaella Zone). This excursion is the best standard for a Cambrian Series 2 base. The oldest West Gondwana trilobite fragments are c. 1 Ma younger than those in Siberia and c. 0.5 Ma older than the oldest Avalonian trilobites (Callavia Zone). This diachrony means a trilobite first appearance datum is an inappropriate chronostratigraphic base for Cambrian Series 2. Taxonomic differences in the oldest trilobites between Cambrian palaeocontinents are in accordance with trace fossil evidence for the group’s appearance possibly as late as c. 530 Ma in the Cambrian Evolutionary Radiation. Coeval 519–517 Ma dates from Avalonia (cool-water siliciclastic shelf) and West Gondwana (tropical carbonate platform) sections with distinct macrofaunas emphasize these successions were latitudinally separate by the late Ediacaran Period.

The Central Asian Orogenic Belt (c. 1000-250 Ma) formed by accretion of island arcs, ophiolites, oceanic islands, seamounts, accretionary wedges, oceanic plateaux and microcontinents in a manner comparable with that of circum-Pacific Mesozoic-Cenozoic accretionary orogens. Palaeomagnetic and palaeofloral data indicate that early accretion (Vendian-Ordovician) took place when Baltica and Siberia were separated by a wide ocean. Island arcs and Precambrian microcontinents accreted to the active margins of the two continents or amalgamated in an oceanic setting (as in Kazakhstan) by roll-back and collision, forming a huge accretionary collage. The Palaeo-Asian Ocean closed in the Permian with formation of the Solonker suture. We evaluate contrasting tectonic models for the evolution of the orogenic belt. Current information provides little support for the main tenets of the one- or three-arc Kipchak model; current data suggest that an archipelago-type (Indonesian) model is more viable. Some diagnostic features of ridge-trench interaction are present in the Central Asian orogen (e.g. granites, adakites, boninites, near-trench magmatism, Alaskan-type mafic-ultramafic complexes, high-temperature metamorphic belts that prograde rapidly from low-grade belts, rhyolitic ash-fall tuffs). They offer a promising perspective for future investigations.

Trilobite moulting behaviour has been extensively investigated. However, exuviae in eodiscid trilobites are poorly known. Here, we report two eodiscid trilobite specimens, Tsunyidiscus niutitangensis and Tsunyidiscus sp., showing Somersault configuration from the Niutitang Formation and Mingxinsi Formation of South China, respectively (Cambrian Series 2, Stage 3). The arrangements of the exoskeletons indicate that the two specimens are the slightly disturbed and undisturbed exuviae. The impression of the lower cephalic unit (LCU) displays the rostral plate in Tsunyidiscus niutitangensis. The exuviae showing the LCU inverted anteriorly under the trunk. The opening of the facial and rostral sutures would have allowed the emergence of the post-ecdysial trilobite with the partial enrolment of exoskeleton. Moreover, our discovery indicates a Somersault configuration which employed the facial and rostral sutures to create an anterior exuvial gape that also exists in eodiscid trilobites besides redlichiid trilobites, corynexochid trilobites and ptychopariid trilobites during the Cambrian.

Selenium (Se) enrichments or deficiency in maize (Zea mays L.), one of the world’s most important staple foods and livestock feeds, can significantly affect many people’s diets, as Se is essential though harmful in excess. In particular, Se-rich maize seems to have been one of the factors that led to an outbreak of selenosis in the 1980s in Naore Valley in Ziyang County, China. Thus, this region’s geological and pedological enrichment offers some insight into the behavior of Se in naturally Se-rich crops. This study examined total Se and Se species in the grains, leaves, stalks, and roots of 11 maize plant samples, Se fractions of soils around the rhizosphere, and representative parent rock materials from Naore Valley. The results showed that total Se concentrations in the collected samples were observed in descending order of soil > leaf > root > grain > stalk. The predominant Se species detected in maize plants was SeMet. Inorganic Se forms, mainly Se(VI), decreased from root to grain, and were possibly assimilated into organic forms. Se(IV) was barely present. The natural increases of Se concentration in soils mainly affected leaf and root dry-weight biomasses of maize. In addition, Se distribution in soils markedly correlated with the weathered Se-rich bedrocks. The analyzed soils had lower Se bioavailability than rocks, with Se accumulated predominantly as recalcitrant residual Se. Thus, the maize plants grown in these natural Se-rich soils may uptake Se mainly from the oxidation and leaching of the remaining organic-sulfide-bound Se fractions. A viewpoint shift from natural Se-rich soils as menaces to possibilities for growing Se-rich agricultural products is also discussed in this study.

AbstractThe stratigraphic distribution of organic-walled microfossils and trace fossils in the Kobrin-1k borehole at the eastern Podlassko-Brest Depression in Belarus was analyzed. The Ryta and Stradech formations host two fossil assemblages (I – with Teophipolia lacerata – Ceratophyton sp., and II – with Retiranus cf. balticus – Sokoloviina costata – Ceratophyton sp.) corresponding to the Rovno–Lontova regional stages of the Lower Cambrian. The data considerably expand the paleontological characteristic of the section and provide new basis for biostratigraphic subdivision and age-estimation of the Vendian–Cambrian transitional interval of the East European Platform.

The natural selenium poisoning due to toxic Se levels in food chain had been observed in humans and animals in Lower Cambrian outcrop areas in Southern Shaanxi, China. To find out the distribution pattern of selenium and other hazardous elements in the plant, soil and water of Lower Cambrian in Southern Shaanxi, China, and their possible potential health risk, a total of 30 elements were analyzed and the health risk assessment of 18 elements was calculated. Results showed that the soil, plant and natural water of Lower Cambrian all had relatively high Se levels. In Lower Cambrian, the soil was enriched with Se, As, Ba, Cu, Mo, Ni, Zn, Ga, Cd and Cr (1.68 < Igeo < 4.48, Igeo; geo-accumulation index). In same plants, the contents of Se, Cd and Zn (except Cd in corn and rice, Zn in potato and corn) of Lower Cambrian were higher than that of the other strata. Ba and Ga in natural water were higher than that of the other strata, while K and Cs were opposite. The health risk assessment results showed that the people living in outcrop areas of Lower Cambrian had both high total non-carcinogenic risk of 18 elements (HI = 16.12, acceptable range: < 1) and carcinogenic risk of As (3.98E−04, acceptable range: 10−6–10−4). High contents of Se, As, Mo and Tl of Lower Cambrian may pose a health risk to local people, and food intake was the major pathway. For minimizing potential health risk, the local inhabitants should use the mix-imported food with local growing foods.

The Ediacaran–Cambrian (E-C) boundary is based on the first appearance of the ichnofossil Treptichnus pedum. Investing an ichnotaxon with such biostratigraphic pre-eminence has been the focus of criticism. Points of contention have revolved around four main issues: (1) ichnotaxonomy, (2) behavioural significance, (3) facies controls and (4) stratigraphic occurrence. First, confusion results from the fact that Treptichnus pedum was originally referred to as Phycodes pedum and, more recently, some authors have placed it in Trichophycus or Manykodes. However, the overall geometry of these burrows indicates they belong in Treptichnus. Second, regardless of its precise mode of feeding, the behaviour involved is iconic of the Cambrian explosion. Third, objections are based on the idea that trace fossils show a closer link to facies than body fossils. Notably, in contrast to common assumptions, T. pedum is not only present in the low-energy offshore of wave-dominated marine settings, but it occurs at considerably shallower water in intertidal and shallow-subtidal zones of tide-dominated systems, as well as in mouth bars of deltaic systems and lower shoreface to offshore transition zones of wave-dominated marine settings. Its broad environmental tolerance supports evolutionary innovations rather than facies controls as the main mechanism underlying the observed vertical pattern of distribution of T. pedum in most E-C successions comprising shallow-marine deposits. Fourth, although treptichnids have been documented below the E-C boundary, T. pedum is not known from Ediacaran rocks. The delayed appearance of T. pedum in E-C successions should be analysed on a case-by-case basis.

Ediacaran and early Cambrian strata in NW Canada contain abundant trace fossils that record the progressive development of complex behavior in early animal evolution. Five feeding groups can be recognized: microbial grazing, deposit-feeding, deposit-feeding/predatory, filter-feeding/predatory, and arthropod tracks and trails. The lower Blueflower Formation (ca. 560–550 Ma) contains abundant burrows that completely cover bedding surfaces with small (∼1 mm diameter) cylindrical burrows that were strictly restricted to microbial bedding surfaces and exhibited only primitive and inconsistent avoidance strategies. The upper Blueflower contains three-dimensional avoidance burrows and rare filter-feeding or possibly predatory burrows, suggesting increased behavioral responses in food gathering that marked the beginning of the agronomic revolution in substrate utilization. Cambrian strata of the Ingta Formation contain systematically meandering burrows and more diverse feeding strategies, including the onset of treptichnid probing burrows that may reflect predation. These observations imply that Ediacaran burrowers were largely characterized by crude, two-dimensional avoidance meanders that represented simple behavioral responses of individual burrowers to sensory information, and that the subsequent development of more diverse and complex feeding patterns with genetically programmed search pathways occurred during the earliest stages of the Cambrian explosion. These observations further imply that changes occurred in both the food source and substrate during the ecological transition from Proterozoic matgrounds to Phanerozoic mixgrounds.