The principles of classification and a classification of mammals. Bulletin of the AMNH ; v. 85

We redescribe the only previously known species of Myrsidea from bulbuls, M. pycnonoti Eichler. Sixteen new species are described; they and their type hosts are: M. phillipsi ex Pycnonotus goiavier goiavier (Scopoli), M. gieferi ex P. goiavier suluensis Mearns, M. kulpai ex P. flavescens Blyth, M. finlaysoni ex P. finlaysoni Strickland, M. kathleenae ex P. cafer (L.), M. warwicki ex Ixos philippinus (J. R. Forster), M. mcclurei ex Microscelis amaurotis (Temminck), M. zeylanici ex P. zeylanicus (Gmelin), M. plumosi ex P. plumosus Blyth, M. eutiloti ex P. eutilotus (Jardine and Selby), M. adamsae ex P. urostictus (Salvadori), M. ochracei ex Criniger ochraceus F. Moore, M. borbonici ex Hypsipetes borbonicus (J. R. Forster), M. johnsoni ex P. atriceps (Temminck), M. palmai ex C. ochraceus, and M. claytoni ex P. eutilotus. A key is provided for the identification of these 17 species.

A new species

Summary Here, the coevolution of mycorrhizal fungi and roots is assessed in the light of evidence now available, from palaeobotanical and morphological studies and the analysis of DNA-based phylogenies. The first bryophyte-like land plants, in the early Devonian (400 million years ago), had endophytic associations resembling vesicular‐ arbuscular mycorrhizas (VAM) even before roots evolved. Mycorrhizal evolution would have progressed from endophytic hyphae towards balanced associations where partners were interdependent due to the exchange of limiting energy and nutrient resources. Most mycorrhizas are mutualistic, but in some cases the trend for increasing plant control of fungi culminates in the exploitative mycorrhizas of achlorophyllous, mycoheterotrophic plants. Ectomycorrhizal, ericoid and orchid mycorrhizas, as well as nonmycorrhizal roots, evolved during the period of rapid angiosperm radiation in the Cretaceous. It is hypothesised that roots gradually evolved from rhizomes to provide more suitable habitats for mycorrhizal fungi and provide plants with complex branching and leaves with water and nutrients. Selection pressures have caused the morphological divergence of roots with different types of mycorrizas. Root cortex thickness and exodermis suberization are greatest in obligately mycorrhizal plants, while nonmycorrhizal plants tend to have fine roots, with more roots hairs and relatively advanced chemical defences. Major coevolutionary trends and the relative success of plants with different root types are discussed.

Coevolution of roots and mycorrhizas of land plants

Geological atlas of western and central Europe

The Cretaceous-Paleogene boundary similar to 65.5 million years ago marks one of the three largest mass extinctions in the past 500 million years. The extinction event coincided with a large asteroid impact at Chicxulub, Mexico, and occurred within the time of Deccan flood basalt volcanism in India. Here, we synthesize records of the global stratigraphy across this boundary to assess the proposed causes of the mass extinction. Notably, a single ejecta-rich deposit compositionally linked to the Chicxulub impact is globally distributed at the Cretaceous-Paleogene boundary. The temporal match between the ejecta layer and the onset of the extinctions and the agreement of ecological patterns in the fossil record with modeled environmental perturbations (for example, darkness and cooling) lead us to conclude that the Chicxulub impact triggered the mass extinction.

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The Chicxulub Asteroid Impact and Mass Extinction at the Cretaceous-Paleogene Boundary

This paper presents an overview of the space and time distributions of Lopingian strata and biotas in Australia, New Zealand, Timor and New Caledonia. Based on this review, we propose a new schematic Late Permian (Lopingian) regional palaeogeographical reconstruction and marine palaeobiogeographical synthesis. The latter also incorporates some key features of the ocean circulation patterns around southeastern Gondwana, inferred primarily from the distribution of regional marine Lopingian faunas. Across Australasia, Lopingian successions accumulated in a wide range of tectonic, palaeoenvironmental and palaeolatitudinal settings. In New Zealand, Lopingian strata are found in several tectonostratigraphical terranes, notably the Brook Street, Dun Mountain–Maitai, Caples, Waipapa and Torlesse terranes/superterranes, each originating as a distinctive basin, island arc or ocean ridge. For the most part, these successions represent displaced segments of volcanic arcs, arc-flanking clastic aprons, intra- and fore-arc basins and accretionary complexes, some of which have been traced via stratigraphical, biostratigraphical and petrological correlations into New Caledonia and eastern Australia. This spectrum of Lopingian tectono-sedimentary environments in New Zealand is interpreted to have been originally located near northeastern Australia on a convergent continental margin (i.e. the Panthalassan margin of southeastern Gondwana). Brachiopod and bivalve faunas occur widely throughout the Lopingian successions of New Zealand and have been closely studied. A total of five successive faunal zones are recognized, ranging in age from mid-late Wuchiapingian to the end of the Changhsingian. In Australia, Lopingian deposits are dominated by non-marine successions in a large number of widely distributed sedimentary basins; onshore exposures of marine deposits are known only from the Gympie Terrane in eastern Australia and the Canning and Bonaparte basins in Western Australia. Lopingian terrestrial sediments are most extensively represented in eastern Australia within a major meridional foreland basin complex (the Tasmania, Sydney, Gunnedah and Bowen basins), for which the evolution through the Lopingian and Early Triassic was governed by the dynamics of the New England Orogen along the Panthalassan margin of southeastern Gondwana. Most of the non-marine successions in eastern Australia are rich in coal measures and plant fossils and locally contain well-preserved non-marine invertebrate and vertebrate fossils. A succession of six palynostratigraphical zones has been recognized in eastern Australia spanning the Lopingian through the Early Triassic. Several of these palynozones have also been recognized in Western Australia, allowing the discrimination and correlation of Lopingian deposits in both onshore and offshore successions. In contrast to eastern Australia and New Zealand, the marine Lopingian successions of Western Australia and Timor are dominated by carbonates that are only locally interbedded with siliciclastic sediments and sparse volcaniclastics; these successions accumulated in a giant sedimentary basin located on a passive and actively rifting continental margin. Marine connections and free and frequent biotic interchanges between this Western Australian superbasin (including Timor) and the Himalayan region of Nepal, southern Tibet and northern India throughout the Lopingian are evident from the shared occurrences of many shallow-marine invertebrate species. Copyright # 2010 John Wiley & Sons, Ltd.

The Lopingian of Australasia : a review of biostratigraphy, correlations, palaeogeography and palaeobiogeography

Single, midrib-positioned galls and midrib-flanking oviposition scars are described from four species of Permian glossopterid foliage from Australia and South Africa. Several of these traces have been mistaken previously for glossopterid reproductive organs or fructification detachment scars. A single Early Triassic corystosperm leaf from Australia is reported bearing multiple disc-like galls on both the midrib and pinnules. A Middle Triassic taeniopterid gymnosperm leaf from Australia is described hosting oviposition scars between consecutive secondary veins flanking the midrib. These fossils attest to a much richer record of plant–arthropod interactions in the late Palaeozoic and early Mesozoic of high-latitude Gondwana than previously reported, and indicate that herbivory and reproductive strategies involving galling and foliar ovipositioning were re-established relatively soon after the end-Permian mass extinction event that saw major turnovers in both the flora and insect fauna.

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New records of leaf galls and arthropod oviposition scars in Permian–Triassic Gondwanan gymnosperms

Early Cretaceous (Neocomian) flora and fauna of the Lower Strzelecki Group, Gippsland Basin, Victoria

Seed ferns, dominant elements of the vegetation in many parts of the world from the Triassic to Cretaceous, were considered to have disappeared at the end of the Cretaceous together with several other groups that had occupied key positions in terrestrial and marine ecosystems such as dinosaurs, plesiosaurs, and ammonoids. Seed-fern demise is generally correlated with competition from diversifying flowering plants through the Cretaceous and the global environmental crisis related to the Chicxulub impact event in the paleotropics at the end of the period. New fossils from Tasmania show that one seed-fern lineage survived into the Cenozoic by at least 13 million years. These fossils are described here as a new species, Komlopteris cenozoicus. Komlopteris is a genus of seed ferns attributed to Corystospermaceae and until now was not known from sediments younger than the Early Cretaceous. Discovery of this "Lazarus taxon," together with the presence of a range of other relictual fossil and extant organisms in Tasmania, other southern Gondwanan provinces, and some regions of northern North America and Asia, underscores high-latitude regions as biodiversity refugia during global environmental crises and highlights their importance as sources of postextinction radiations.

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Seed ferns survived the end-cretaceous mass extinction in Tasmania

Molecular phylogenetic studies of extant organisms have shown that those branches of the Bacteria and Archaea that lie closest to the “last common ancestor” of all life are occupied by hyperthermophiles. At the same time, the search for former life on Mars has focussed on thermal spring deposits. For these reasons there is interest in the palaeobiology of ancient thermal spring deposits on Earth. Many such deposits are known but very few have been studied by palaeobiologists. The Devonian sinters of the Drummond Basin, Australia, rank with the Rhynie cherts of Scotland as the oldest well established examples of fossil subaerial hot springs. The Drummond Basin sinters are closely comparable with modem examples in Yellowstone National Park, Wyoming, and elsewhere. It is possible to recognise a range of palaeoenvironments from high temperature vents through former hot-water channelways and terraces to ambient temperature marsh deposits. Cyanobacterial stromatolites and microfossils are abundant in those palaeoenvitronments characterised by temperatures well above ambient, and the marsh and other ambient temperature palaeoenvironments contain abundant herbaceous lycopsids and sphenopsids encrusted by microbial overgrowths. © 1998 Association of Australasian Palaeontologists.

Stephen McLoughlin

Papers

The Lopingian of Australasia : a review of biostratigraphy, correlations, palaeogeography and palaeobiogeography

New records of leaf galls and arthropod oviposition scars in Permian–Triassic Gondwanan gymnosperms

Early Cretaceous (Neocomian) flora and fauna of the Lower Strzelecki Group, Gippsland Basin, Victoria

Seed ferns survived the end-cretaceous mass extinction in Tasmania

Palaeontology of Devonian thermal spring deposits, Drummond Basin, Australia