Crustal and upper mantle seismic structure of the Australian Plate, South Island, New Zealand

Seismic reflection and refraction data were collected west of New Zealand's South Island parallel to the Pacific–Australian Plate boundary. The obliquely convergent plate boundary is marked at the surface by the Alpine Fault, which juxtaposes continental crust of each plate. The data are used to study the crustal and uppermost mantle structure and provide a link between other seismic transects which cross the plate boundary. Arrival times of wide-angle reflected and refracted events from 13 recording stations are used to construct a 380-km long crustal velocity model. The model shows that, beneath a 2–4-km thick sedimentary veneer, the crust consists of two layers. The upper layer velocities increase from 5.4–5.9 km/s at the top of the layer to 6.3 km/s at the base of the layer. The base of the layer is mainly about 20 km deep but deepens to 25 km at its southern end. The lower layer velocities range from 6.3 to 7.1 km/s, and are commonly around 6.5 km/s at the top of the layer and 6.7 km/s at the base. Beneath the lower layer, the model has velocities of 8.2–8.5 km/s, typical of mantle material. The Mohorovicic discontinuity (Moho) therefore lies at the base of the second layer. It is at a depth of around 30 km but shallows over the south–central third of the profile to about 26 km, possibly associated with a southwest dipping detachment fault. The high, variable sub-Moho velocities of 8.2 km/s to 8.5 km/s are inferred to result from strong upper mantle anisotropy. Multichannel seismic reflection data cover about 220 km of the southern part of the modelled section. Beneath the well-layered Oligocene to recent sedimentary section, the crustal section is broadly divided into two zones, which correspond to the two layers of the velocity model. The upper layer (down to about 7–9 s two-way travel time) has few reflections. The lower layer (down to about 11 s two-way time) contains many strong, subparallel reflections. The base of this reflective zone is the Moho. Bi-vergent dipping reflective zones within this lower crustal layer are interpreted as interwedging structures common in areas of crustal shortening. These structures and the strong northeast dipping reflections beneath the Moho towards the north end of the (MCS) line are interpreted to be caused by Paleozoic north-dipping subduction and terrane collision at the margin of Gondwana. Deeper mantle reflections with variable dip are observed on the wide-angle gathers. Travel-time modelling of these events by ray-tracing through the established velocity model indicates depths of 50–110 km for these events. They show little coherence in dip and may be caused side-swipe from the adjacent crustal root under the Southern Alps or from the upper mantle density anomalies inferred from teleseismic data under the crustal root.     

Using stable isotope analyses to assess carbon dynamics in a shallow subtropical estuary

The sources of carbon, which fuel water column respiration, remain unresolved for most estuaries; our objective was to examine carbon dynamics in a shallow subtropical estuary. We sampled the Sabine-Neches estuary, Texas, during low (November 1999) and high (May 2000) freshwater inflow and measured stable carbon isotope ratios of the dissolved inorganic and orgnaic carbon (δ¹³C-DIC, δ¹³C-DOC), as well as quantifying accessory parameters (salinity, nutrients, total suspended solids, and photosynthetic pigments). Pigment analysis indicated that diatoms were the predominant phytoplankton. Data from the May 2000 sampling event exhibited conservative mixing, indicating that the system was acting as a conduit between the watershed and the Gulf of Mexico. During November, mixing was generally nonconservative indicating extensive recycling of allochthonous and autochthonous carbon sources. Our data imply that both carbon sources had similar isotope, ratios that made it impossible to unambiguously determine the dominant source supporting respiration. The nonconservative DIC concentration data indicating an autotrophic sink as well as the strong relationship between δ¹³C-DOC and chlorophylla, suggest that in situ production was an important component of the DOC pool. We hypothesize that uncharacteristically calm wind conditions during sampling may have promoted phytoplankton settling, removing autotrophs, from the water column, but leaving behind a dissolved biogeochemical signature. Interpretation of carbon dynamics may be confounded by spatial and temporal decoupling of producers and consumers from biogeochemical indicators.     

Did Paleogene North Atlantic rift-related eruptions drive early Eocene climate cooling?

The delivery of volcanogenic sulphur into the upper atmosphere by explosive eruptions is known to cause significant temporary climate cooling. Therefore, phreatomagmatic and phreatoplinian eruptions occurring during the final rifting stages of active flood basalt provinces provide a potent mechanism for triggering climate change.

During the early Eocene, the northeast Atlantic margin was subjected to repeated ashfall for 0.5 m.y. This was the result of extensive phreatomagmatic activity along 3000 km of the opening northeast Atlantic rift. These widespread, predominantly basaltic ashes are now preserved in marine sediments of the Balder Formation and its equivalents, and occur over an area extending from the Faroe Islands to Denmark and southern England. These ash-bearing sediments also contain pollen and spore floras derived from low diversity forests that grew in cooler, drier climates than were experienced either before or after these highly explosive eruptions. In addition, coeval plant macrofossil evidence from the Bighorn Basin, Wyoming, USA, also shows a comparable pattern of vegetation change. The coincidence of the ashes and cooler climate pollen and spore floras in northwest Europe identifies volcanism as the primary cause of climate cooling. Estimates show that whilst relatively few phreatomagmatic eruptive centres along the 3000 km opening rift system could readily generate 0.5–1 °C cooling, on an annual basis, only persistent or repeated volcanic phases would have been able to achieve the long-term cooling effect observed in the floral record. We propose that the cumulative effect of repeated Balder Formation eruptions initiated a biodiversity crisis in the northeast Atlantic margin forests. Only the decline of this persistent volcanic activity, and the subsequent climatic warming at the start of the Eocene Thermal Maximum allowed the growth of subtropical forests to develop across the region.     

Revision of the conchostracan genus Estherites from the Upper Cretaceous Nenjiang Formation of the Songliao Basin and its biogeographic significance in China

The diagnosis of Estherites corrugatus from the basal part of the Coniacian Second Member of the Nenjiang Formation in Nenjiang County, north-east China is revised following the application of a new preparation technique to some of the carapaces and an examination of specimens under a scanning electron microscope, both of which revealed morphological features on the carapace that had not been recognized previously. Restudy of the type species of the two subgenera Estherites (Euestherites) and Estherites (Parestherites) also revealed details of carapace features not seen hitherto. These indicate that they should be separated from Estherites. As a result, Euestherites is upgraded to genus level and Parestherites is placed in synonymy. The importance of Estherites and Euestherites is considered in the context of Late Cretaceous assemblages of these crustaceans and the three conchostracan provinces (South-West, South-East and North China) that are recognized to have been present in China during the Turonian–Santonian period.     

Pronounced occurrence of long-chain alkenones and dinosterol in a 25,000-year lipid molecular fossil record from Lake Titicaca, South America

Our analysis of lipid molecular fossils from a Lake Titicaca (16° S, 69° W) sediment core reveals distinct changes in the ecology of the lake over an ∼25,000-yr period spanning latest Pleistocene to late Holocene time. Previous investigations have shown that over this time period Lake Titicaca was subject to large changes in lake level in response to regional climatic variability. Our results indicate that lake algal populations were greatly affected by the changing physical and chemical conditions in Lake Titicaca. Hydrocarbons are characterized by a combination of odd-numbered, mid- to long-chain (C₂₁-C₃₁) normal alkanes and alkenes. During periods when lake level was higher (latest Pleistocene, early Holocene, and late Holocene), the C₂₁n-alkane, and the C₂₅ and C₂₇ alkenes dominate hydrocarbon distributions and indicate contribution from an algal source, potentially the freshwater alga Botryococcus braunii. The C₃₀ 4 α-methyl sterol (dinosterol) increases sharply during the mid-Holocene, suggesting a greatly increased dinoflagellate presence at that time. Long-chain alkenones (LCAs) become significant during the early Holocene and are highly abundant in mid-Holocene samples. There are relatively few published records of LCA detection in lake sediments but their occurrence is geographically widespread (Antarctica, Asia, Europe, North America). Lake Titicaca represents the first South American lake and the first low-latitude lake in which LCAs have been reported. LCA abundance and distribution may be related to the temperature-dependent response of an unidentified algal precursor. Although the LCA unsaturation indices cannot be used to determine absolute Lake Titicaca temperatures, we suspect that the published LCA U₃₇^K unsaturation calibrations can be applied to infer relative temperatures for early to mid-Holocene time when LCA concentrations are high. Using these criteria, the U₃₇^K unsaturation indices suggest relatively warmer temperatures in the mid-Holocene. In contrast to previous speculation, lipid analysis provides little evidence of a greatly increased presence of aquatic plants during the mid-Holocene. Instead, it appears that a few algal species were dominant in the lake. Based on the dramatic rise in abundances of LCAs and dinosterol during the early to mid-Holocene, we suspect that the algal producers of these compounds rose in response to a combination of physical and chemical changes in the lake. These include temperature, salinity, and alkalinity changes that occurred as lake level dropped sharply during a multi-millennial drought affecting the Central Andean Altiplano.     

Electronic structures of iron(III) and manganese(IV) (hydr)oxide minerals: Thermodynamics of photochemical reductive dissolution in aquatic environments

Sunlight-induced reduction and dissolution of colloidal Fe-Mn (hydr)oxide minerals yields elevated concentrations of Fe²⁺ and Mn²⁺ in natural waters. Since these elements may be biolimiting micronutrients, photochemical reactions might play a significant role in biogeochemical cycles. Reductive photodissolution of Fe (hydr)oxide minerals may also release sorbed metals. The reactivity of Fe-Mn (hydr)oxide minerals to sunlight-induced photochemical dissolution is determined by the electronic structure of the mineral-water interface. In this work, oxygen K-edge absorption and emission spectra were used to determine the electronic structures of iron(III) (hydr)oxides (hematite, goethite, lepidocrocite, akaganeite and schwertmannite) and manganese(IV) oxides (pyrolusite, birnessite, cryptomelane). The band gaps in the iron(III) (hydr)oxide minerals are near 2.0-2.5 eV; the band gaps in the manganese (IV) oxide phases are 1.0-1.8 eV. Using published values for the electrochemical flat-band potential for hematite together with experimental pH_pzc values for the (hydr)oxides, it is possible to predict the electrochemical potentials of the conduction and valence bands in aqueous solutions as a function of pH. The band potentials enable semiquantitative predictions of the susceptibilities of these minerals to photochemical dissolution in aqueous solutions. At pH 2 (e.g., acid-mine waters), photoreduction of iron(III) (hydr)oxides could yield millimolal concentrations of aqueous Fe²⁺ (assuming surface detachment of Fe²⁺ is not rate limiting). In seawater (pH 8.3), however, the direct photo-reduction of colloidal iron(III) (hydr)oxides to give nanomolal concentrations of dissolved, uncomplexed, Fe²⁺ is not thermodynamically feasible. This supports the hypothesis that the apparent photodissolution of iron(III) (hydr)oxides in marines systems results from Fe³⁺ reduction by photochemically produced superoxide. In contrast, the direct photoreduction of manganese oxides should be energetically feasible at pH 2 and 8.3.