Multi-technique approach to characterise the effects of cryopreservation on larval development of the Pacific oyster (Crassostrea gigas)

Cryopreservation experiments were conducted on D-stage larvae of the Pacific oyster (Crassostrea gigas) to investigate the effects of two cryoprotectant solutions and three cooling rates on larval development from 1 to 22 days post-fertilisation. Cryoprotectant solutions were made up to final concentrations (after 1:1 dilution with larvae) of 10% ethylene glycol, 1% polyvinylpyrrolidone and either 0.2 or 0.4 M trehalose. Three cooling rates (0.5, 1 and 2 °C min^?1 between ?10 and ?35 °C post-holding) were tested in an orthogonal design with the two cryoprotectants. Results indicate that control larvae out-performed all cryopreservation treatments for survival, feeding consumption and shell length parameters. However, larvae exposed to 0.4 M trehalose did considerably better than those exposed to 0.2 M trehalose, regardless of cooling rate conditions. Scanning electron and light microscopy observations were used to assess larval morphology and organogenesis, indicating that treatments with surviving larvae were morphologically and developmentally similar to control larvae.     

Bank-derived carbonate sediment transport and dissolution in the Hawaiian Archipelago

This investigation used two approaches to examine the flux of bank-derived carbonate particles and determine the potential influence of benthic carbonate particle dissolution on the carbon chemistry of the waters around the Hawaiian Archipelago. First, the particle flux near several representative carbonate banks in the Hawaiian Archipelago was measured and compared with the flux at a distal site (ALOHA) approximately 100 km north of Oahu, Hawaii. The results of four sediment trap deployments on three carbonate banks in the Hawaiian Archipelago demonstrate that the flux of bank-derived carbonate particles are consistently one to two orders of magnitude higher than the fluxes at the distal station. Furthermore, the mineralogy of the carbonate flux near the banks, which includes very soluble bank-derived aragonite and magnesian calcite particles, is distinctly different from that of the distal fluxes. Second, the chemistry of the waters at each bank station along the archipelago was characterized and compared with the chemistry of the distal waters to determine if differences in the particle flux were reflected in the carbon chemistry. Higher alkalinity and carbonate ion concentrations were observed around all of the banks studied. The saturation state of these waters suggests that the dissolution of some magnesian calcite and aragonite phases could explain the higher alkalinity values. Calculations suggest that the dissolution of benthically-derived aragonite and magnesian calcite may be an important component of the North Pacific alkalinity budget and a potential sink for anthropogenic CO₂.     

Molecular parameters of maturation in the Toarcian shales,Paris Basin,France—I. Changes in the configurations of acyclic isoprenoid alkanes,steranes and triterpanes

The changes in configuration at a number of chiral centres in certain acyclic isoprenoid alkanes, steranes, rearranged steranes and triterpanes of the hopane type in a suite of fourteen Toarcian shales (Paris Basin) have been determined by gas chromatography and combined gas chromatography-mass spectrometry. A sequence of changes in the ratios of various stereoisomers occurs both with increasing maximum depth of burial and in a North-South direction for shallow samples (maximum burial depth < 1000m). These changes cover the full range of maturity shown by the samples. The presence of 5α(H), 14β(H), 17β(H)-steranes in immature samples indicates the presence of a reworked component. The extent of epimerisation at a number of the chiral centres suggests that it relates to the extent of steric hindrance at the centres.     

A MULTIBLOCK PARTIAL LEAST SQUARES ALGORITHM FOR INVESTIGATING COMPLEX CHEMICAL SYSTEMS

The details of a general multiblock partial least squares(PLS)algorithm based on one originallypresented by Wold et al.have been developed and are completely presented.The algorithm can handlemost types of relationships between the blocks and constitutes a significant advancement in the modelingof complex chemical systems.The algorithm has been programmed in FORTRAN and has been testedon two simulated multiblock problems,a three-block and a five-block problem.The algorithm combinesthe score vectors for all blocks predicting a particular block into a new block.This new block is used topredict the predicted block in a manner analogous to the two-block PLS.In a similar manner if one blockpredicts more than one other block,the score vectors of all predicted blocks are combined to form a newblock,which is then predicted by the predictor block as in the two-block PLS.Blocks that both predictand are predicted are treated in such a way that both of these roles can be taken into account whencalculating interblock relationships.The results of numerical simulations indicate that the computerprogram is operating properly and that the multiblock PLS produces meaningful and consistent results.     

Shoshonitic and calc-alkaline lavas from the Highlands of Papua New Guinea

Pleistocene to Recent stratovolcanoes in the Highlands of Papua New Guinea are made up of calc-alkaline to shoshonitic lava, tuff, agglomerate, ash, and lahar deposits. The volcanic rocks are characterized by high and variable Al, high K and total alkalis, and low Fe, Mg, and Ca. There is a continuous variation between high-K calc-alkaline, low-Si high-K calc-alkaline, and shoshonitic rocks. The elements V, Rb, Sr, Zn, Nb, and Ba are high relative to general andesitic abundances, particularly in the shoshonites. The Highlands volcanic rocks originated either in the base of thick sialic crust which is undergoing stabilization after major orogeny and uplift, or more probably, in eclogite sinking through the underlying mantle. Variation in content of K and other incompatible elements was either inherited from the source rocks in the base of the crust, or was produced by zone refining in a thick upper mantle zone containing interstitial fluid rich in these elements. Further variation, mainly in Fe/Mg, Si, and total alkalis, was caused by minor low-pressure crystal fractionation involving olivine, clinopyroxene, and, to a lesser extent, calcic plagioclase.     

Comparison of CO2 Dynamics and Air–Sea Gas Exchange in Differing Tropical Reef Environments

An array of MAPCO₂ buoys, CRIMP-2, Ala Wai, and Kilo Nalu, deployed in the coastal waters of Hawaii, have produced multi-year high temporal resolution CO₂ records in three different coral reef environments off the island of Oahu, Hawaii. This study, which includes data from June 2008 to December 2011, is part of an integrated effort to understand the factors that influence the dynamics of CO₂–carbonic acid system parameters in waters surrounding Pacific high-island coral reef ecosystems and subject to differing natural and anthropogenic stresses. The MAPCO₂ buoys are located on the Kaneohe Bay backreef, and fringing reef sites on the south shore of Oahu, Hawaii. The buoys measure CO₂ and O₂ in seawater and in the atmosphere at 3-h intervals, as well as other physical and biogeochemical parameters (conductivity, temperature, depth, chlorophyll-a, and turbidity). The buoy records, combined with data from synoptic spatial sampling, have allowed us to examine the interplay between biological cycles of productivity/respiration and calcification/dissolution and biogeochemical and physical forcings on hourly to inter-annual time scales. Air–sea CO₂ gas exchange was also calculated to determine whether the locations were sources or sinks of CO₂ over seasonal, annual, and interannual time periods. Net annualized fluxes for CRIMP-2, Ala Wai, and Kilo Nalu over the entire study period were 1.15, 0.045, and ?0.0056 mol C m^?2 year^?1, respectively, where positive values indicate a source or a CO₂ flux from the water to the atmosphere, and negative values indicate a sink or flux of CO₂ from the atmosphere into the water. These values are of similar magnitude to previous estimates in Kaneohe Bay as well as those reported from other tropical reef environments. Total alkalinity (A_T) was measured in conjunction with pCO₂, and the carbonic acid system was calculated to compare with other reef systems and open ocean values around Hawaii. These findings emphasize the need for high-resolution data of multiple parameters when attempting to characterize the carbonic acid system in locations of highly variable physical, chemical, and biological parameters (e.g., coastal systems and reefs).     

Burial and Preservation of Carbonate Rocks Over Phanerozoic Time

Comparison of results for the original burial rate of carbonate sediments over Phanerozoic time, as calculated using the GEOCARBSULFvolc model, with their rate of preservation to the present (survival rate) shows a considerable loss of mass, partly by subduction of oceanic crust, during the past 250 million years. Before that time, despite the evidence that preserved Paleozoic carbonates appear to have been deposited only in shallow water, we contend that there was also inorganic deposition of carbonates in the Paleozoic deep sea with subsequent loss by subduction. Inorganic carbonate deposition may have been abetted by the vastly different seawater and atmospheric composition for most of the Paleozoic than those of post-Cretaceous and end Paleozoic–early Mesozoic times. The hypothesis helps to explain the loss of mass greater than that predicted for shallow-water carbonates prior to 250 Ma.