Ian P. Wilkinson

Megatsunami deposits on Kohala volcano, Hawaii, from flank collapse of Mauna Loa

The origin of coastal and high-elevation marine gravels on the Hawaiian islands of Lanai and Molokai is controversial, because the vertical tectonics of these islands is poorly constrained. The gravels are either from eustatic highstands or were left by massive tsunamis from offshore giant landslides. In contrast, at Kohala on the island of Hawaii, where continuous subsidence is well established, lithofacies analysis and dating of a fossiliferous marine conglomerate 1.5–61 m above present sea level support a tsunami origin and indicate a runup of >400 m >6 km inland. The conglomerate age, 110 ± 10 ka, suggests a tsunami caused by the ca. 120 ka giant Alika 2 landslide from nearby Mauna Loa volcano.

A record of late Cenozoic stratigraphy, sedimentation and climate change from the Hebrides Slope, NE Atlantic Ocean

A punctuated 103.3 m thick succession of upper Palaeogene to Quaternary sediments has been recovered in a borehole from the upper Hebrides Slope, west of Britain. The borehole proved 11.2m of upper Oligocene, carbonate-rich muds at the base, unconformably overlain by 2.85 m of middle to upper Miocene, glauconitic sands. This is in turn unconformably overlain by 89.25 m of predominantly Plio-Pleistocene sands and muds, with a Holocene sea-bed veneer. The post-Miocene succession is subdivided into two units: the sand-dominated, Pliocene to lower middle Pleistocene, Lower MacLeod sequence between 89.25 and 67.82 m, and the mud-dominated, middle Pleistocene to Holocene, Upper MacLeod sequence above 67.82 m. Regional mapping indicates that these sequences are commonly associated with large-scale shelf-margin progradation and slope-front fan construction. The borehole core provides an excellent record of the transition from pre-glacial to glacial conditions in the mid-latitude NE Atlantic Ocean. Climatic conditions warmer than present prevailed in the late Oligocene, mid- to late Miocene and Pliocene, although the influx of ice-rafted detritus in the late Pliocene marks the onset of climatic deterioration. This deterioration continued, in a fluctuating manner, until the early mid-Pleistocene (0.44 Ma) when fully glacial conditions were established on the Hebridean Margin.

Ostracoda and palaeo-oxygen levels, with particular reference to the Upper Cretaceous of East Anglia

Abstract It has been shown that the percentage of Platycopina (the sole remaining group of filter-feeding Ostracoda since the global extinction of the Metacopina in the Lower Toarcian) making up a fossil ostracod fauna can be used as a measure of dissolved oxygen in past oceans. High levels of platycopids indicate low oxygen and vice versa. A new scale is introduced here, based mainly on the environmental oxygen levels of modern oceans and their equivalent percentages of living platycopids, in order to evaluate the palaeo-oxygen levels of the Upper Chalk in East Anglia. The effects of varying oxygen concentrations on the overall simple species diversity of the Ostracoda is also shown to have important palaeoenvironmental implications. The study is based on 79 samples from the Santonian to Lower Maastrichtian of the Trunch Borehole and 126 samples from outcrops in Suffolk and Norfolk, ranging from the Coniacian to Lower Maastrichtian. The Coniacian is shown to have been a time of low to very low oxygen, except for its upper part that was much better ventilated. The Santonian and Lower Campanian were low to very low in their dissolved oxygen, while the Upper Campanian and particularly the Lower Maastrichtian had much higher oxygen levels. Notwithstanding these general trends, oxygen levels appear to have fluctuated rapidly throughout the interval, during times of both generally low and high oxygenation. These variations in oxygenation are thought to have been associated with the Oxygen Minimum Zone and its migrations onto the continental shelf and subsequent retreat to the continental slope. This in turn is related to sea-level fluctuations and this, together with the potential for the application of this technique to sequence stratigraphy are discussed.

Early Carboniferous (Late Tournaisian-Early Viséan) ostracods from the Ballagan Formation, central Scotland, UK

The Ballagan Formation (Late Tournaisian–Early Viséan) of central Scotland yields an ostracod fauna of 14 species in ten genera, namely Beyrichiopsis, Cavellina, Glyptolichvinella, Glyptopleura, Knoxiella, Paraparchites, Sansabella, Shemonaella, Silenites and Sulcella. The ostracods, in combination with palynomorphs, are important biostratigraphical indices for correlating the rock sequences, where other means of correlation, especially goniatites, conodonts, foraminifera, brachiopods or corals are absent. Stratigraphical distribution of the ostracods, calibrated with well-established palynomorph biozones, identifies three informally defined intervals: a sub-CM palynomorph Biozone interval with poor ostracod assemblages including Shemonaella scotoburdigalensis; a succeeding interval within the CM palynomorph Biozone where Cavellina coela, Cavellina incurvescens, Sansabella amplectans and the new species Knoxiella monarchella and Paraparchites discus first appear; and, an upper interval, in the upper CM Biozone, marked by the appearance of Sulcella affiliata. At least locally in central Scotland, S. affiliata permits a level of resolution equivalent to a sub-zonal upper division of the CM Biozone. The fauna, flora, sedimentology and stable isotope composition (δ13C and δ18O) of carbonate minerals in the Ballagan Formation suggest the ostracods inhabited brackish, hypersaline and ephemeral aquatic ecologies in a coastal floodplain setting.

Ostracods from freshwater and brackish environments of the Carboniferous of the Midland Valley of Scotland: the early colonization of terrestrial water bodies

The Mississippian Strathclyde Group of the Midland Valley of Scotland yields some of the earliest non-marine ostracods. The succession records shallow marine, deltaic, estuarine, lagoonal, lacustrine, fluvial and swamp environments representing a series of staging-posts between fully marine and limnetic settings. Macrofossils and ostracods are assigned to marine, marginal marine, brackish and freshwater environments based on their faunal assemblage patterns. Key brackish to freshwater ostracods are Geisina arcuata , Paraparchites circularis n. sp., Shemonaella ornata n. sp. and Silenites sp. A, associated with the bivalves Anthraconaia , Carbonicola , Cardiopteridium , Curvirimula , Naiadites , the microconchid ‘ Spirorbis ’, Spinicaudata and fish. Many Platycopina and Paraparchiticopina ostracods are interpreted as euryhaline, which corresponds with their occurrence in marine to coastal plain water bodies, and supports the ‘estuary effect’ hypothesis of non-marine colonization. The success of non-marine colonization by ostracods was dependent on the intrinsic adaptations of ostracod species to lower salinities, such as new reproductive strategies and the timing of extrinsic mechanisms to drive non-marine colonization, such as sea-level change. The genus Carbonita is the oldest and most common freshwater ostracod, and went on to dominate freshwater environments in the Late Palaeozoic.

Efficacy of δ18O data from Pliocene planktonic foraminifer calcite for spatial sea surface temperature reconstruction: comparison with a fully coupled ocean–atmosphere GCM and fossil assemblage data for the mid-Pliocene

Sea surface temperature (SST) estimates using the δ18O composition of fossil planktonic foraminifer calcite, within the time slice 3.12 to 3.05 Ma (Pliocene, Kaena Subchron – C2An1r) are assessed for nine Atlantic Ocean sites. These are compared with SST estimates from fossil assemblages for the ‘Time Slab’ 3.29–2.97 Ma and with estimates from a fully coupled ocean–atmosphere General Circulation Model (GCM) for the same time interval. Most SST estimates derived from the δ18O data indicate a cooler ocean surface than at present, through the latitudinal range 69.25° N to 46.88° S. At some sites the temperature difference is greater than 5 °C (cooler than at present). This contrasts with SST estimates from fossil assemblages that give warmer than present temperatures at mid- to high latitudes, and similar temperatures in the tropics, and with the GCM, which predicts SSTs warmer than at present across all latitudes for this time interval. Difficulties interpreting the ecology of fossil foraminifer assemblages and inaccurate estimates of mid-Pliocene seawater δ18O composition (δ18Osw) at some sites may partly produce the temperature discrepancy between isotope-based and fossil-based SST estimates, but do not adequately explain the cool signal of the former. We interpret the cool SST estimates from the δ18O data to be the product of: (a) calcite formed at a level deep within or below the ocean mixed-layer during the life-cycle of the foraminifera; (b) secondary calcite with higher δ18O formed in the planktonic foraminifer tests in sea bottom pore waters. Although these effects differ between sites, secular and temporal oceanographic trends are preserved in the primary calcite formed in the mixed-layer near the ocean surface, witnessed by the latitudinal variation in estimated SSTs. Reconstructing accurate mid-Pliocene SSTs with much of the existing published oxygen isotope data probably requires a detailed re-assessment of taphonomy, particularly at tropical sites. This study also indicates that methods for estimating Atlantic Pliocene δ18Osw need to be refined.

Exceptionally preserved ostracodes from a Middle Miocene palaeolake, California, USA

Abstract: Exceptionally well-preserved specimens of a new cypridid ostracode (Crustacea), Raepula ira sp. nov., are described from palaeolake sediments of the Middle Miocene Barstow Formation of the Mud Hills, southern California. This is only the second occurrence of exceptionally preserved ostracodes from the Miocene. Based on ages obtained from associated volcanic tuffs the palaeolake sediments were deposited between 16.3 and 15.8 Ma. The ostracodes form one element of a diverse lake community dominated by fairy shrimps, copepods, diatoms, larvae of diving beetles, flies and mosquitoes, and body fossils and ephippia of branchiopods and anomopods. The ostracodes are preserved three dimensionally with their soft anatomy replicated in microcrystalline silica. Submicron-scale details such as sensory setae are preserved, surpassing the resolution of most other ostracode-bearing lagerstätten and allowing their biology to be compared with extant taxa. Supplementary material: Red–blue anaglyphs of the exceptionally preserved ostracodes are available at http://www.geolsoc.org.uk/SUP18407.

Micropalaeontology reveals the source of building materials for a defensive earthwork (English Civil War?) at Wallingford Castle, Oxfordshire

Microfossils recovered from sediment used to construct a putative English Civil War defensive bastion at Wallingford Castle, south Oxfordshire, provide a biostratigraphical age of Cretaceous (earliest Cenomanian) basal M. mantelli Biozone. The rock used in the buttress – which may have housed a gun emplacement – can thus be tracked to the Glauconitic Marl Member, base of the West Melbury Marly Chalk Formation. A supply of this rock is available on the castle site or to the east of the River Thames near Crowmarsh Gifford. Microfossils provide a unique means to provenance construction materials used at the Wallingford site. While serendipity may have been the chief cause for use of the Glauconitic Marl, when compacted, it forms a strong, almost ‘road base’-like foundation that was clearly of use for constructing defensive works. Indeed, use of the Glauconitic Marl was widespread in the area for agricultural purposes and its properties may have been well-known locally.

Ostracod carnivory through time

Carnivory in modern ostracods takes the form of predation, scavenging and parasitism. In the fossil record, carnivory is difficult to prove without the fossilisation of diagnostic functional morphological features or the preservation of the intimate association between the ostracods and the carrion or prey. Six examples of putative carnivory are known in geological deep time, the most persuasive being scavenging myodocopes of Ordovician, Carboniferous and Triassic ages (Myodoprimigenia, Eocypridina and Triadocypris), where swarms of ostracods are found associated with carcasses, and the early Silurian Colymbosathon in which characteristic soft part anatomy is preserved. Other putative scavengers, such as late Jurassic Juralebris, are unlikely to be carnivorous.

Kimmeridge Clay Ostracoda of the North Wootton Borehole, Norfolk, England

Ostracoda from the Kimmeridge Clay Formation (Upper Jurassic) of the North Wootton Borehole was examined from a biostratigraphical point of view. The ostracod zonal scheme, previously erected for the stratotype section in Dorset, is modified and the faunas are related to the 47 beds which can be recognised by a combination of macrofaunal and lithological characteristics. Seven ostracod assemblage zones are recognised in the borehole, of these three are new and one is subdivided into two subzones. One new genus, Micrommatocythere, together with four new species and one new subspecies–Micrommatocythere edmundi, Paranotacythere (Unicosta) effusa, Mandelstamia (Xeromandelstamia) horrida, Macrodentina (Polydentina) woottonensis and Galliaecytheridea mandelstami kilenyii–are described.