Evaluation of mussel immune responses as indicators of contamination in San Francisco Bay

Several immune parameters were evaluated in two species of mussels (Mytilus californianus and M. galloprovincialis/M. trossulus) as bioindicators of contaminant effects. The mussels were deployed in San Francisco Bay Estuary and a control site at Bodega Marine Laboratory. Assays for phagocytosis and phagocytic index (average number of particles engulfed per hemocyte) were conducted with hemocytes in their own hemolymph-the "Serum" method. The responses were compared with contaminant concentrations in those mussels. For both species, the contaminated South Bay Dumbarton Bridge and Redwood Creek sites had elevated phagocytosis relative to the Bodega control site, indicating contaminant stress. The results also showed that M. californianus had higher percentages of phagocytosis (74%) and a higher phagocytic index (4.6 particles per cell) than those of M. galloprovincialis/M. trossulus (60% phagocytosis and 3.5 particles per cell). As there is a difference in immune response to contaminants, it is suggested that future San Francisco Estuary monitoring should be conducted with endemic M. galloprovincialis/M. trossulus rather than with the currently utilized M. californianus, which is not found in the estuary.     

The effects of fire on rock weathering: some further considerations of laboratory experimental simulation

Fire in the natural environment is a widespread agent of geomorphological and biological change. Temperatures can exceed 1000°C. There is often a rapid rise from ambient conditions through a steep thermal gradient, promoting rock disintegration. Laboratory simulation studies have established that temperature changes which are representative of natural fires affect rock material properties, which can then be related to weathering susceptibility. This study extends previous work by more closely replicating the natural environment, (a) through the simulation of rainfall and (b) by encasing samples to reflect the exposure of a single rock face to a passing fire event. Rock samples collected on Cyprus were prepared and tested following previously reported procedures. Change in modulus of elasticity was monitored using a non-destructive ultrasonic method. The data corroborate previous work but with somewhat different degrees of change. The new results are more likely to be representative of natural conditions and real-world change. The rate of rock disintegration and effects such as case-hardening appear to be a function of rock thermal characteristics, material properties and environmental constraints such as diurnal temperature range. Copyright © 1999 John Wiley & Sons, Ltd.     

A new map of the Mitdluagkat glacier—a preliminary report

Hasholt, Bent: A new map of the Mitdluagkat glacier—a preliminary report. Geografisk Tidsskrift 87: 19–21, Copenhagen June 1987.

A new map covering the whole Mitdluagkat Glacier has been elaborated. The map is based on air photos from Geodetic Institute in scale 1:150,000 taken July 30, 1981. The scale of the new map is 1:20,000 with 10-m contour intervals. Preliminary field tests indicate that the map is so accurate that it might be used for comparative studies of long-term variations in mass balance of the glacier.     

δB, Sr, Mg and B in a modern Porites coral: the relationship between calcification site pH and skeletal chemistry

Sr/Ca, B/Ca, Mg/Ca and δ¹¹B were determined at high spatial resolution across ∼1 year of a modern Hawaiian Porites lobata coral by secondary ion mass spectrometry (SIMS). We observe significant variations in B/Ca, Mg/Ca, Sr/Ca and δ¹¹B over short skeletal distances (nominally equivalent to periods of <20 days). This heterogeneity probably reflects variations in the composition of the extracellular calcifying fluid (ECF) from which the skeleton precipitates. Calcification site pH (total scale) was estimated from skeletal δ¹¹B and ranged from 8.3 to 8.8 (± ∼0.1) with a mean of ∼8.6. Sr/Ca and B/Ca heterogeneity is not simply correlated with calcification site pH, as might be expected if Ca-ATPase activity increases the pH and decreases the Sr/Ca and B(OH)₄⁻/CO₃²⁻ ratios of the ECF. We produced a simple model of the ECF composition and the skeleton deposited from it, over a range of calcium transport and carbonate scenarios, which can account for these observed geochemical variations. The relationship between the pH and Sr/Ca of the ECF is dependent on the concentration of DIC at the calcification site. At higher DIC concentrations the ECF has a high capacity to buffer the [H⁺] changes induced by Ca-ATPase pumping. Conversely, at low DIC concentrations, this buffering capacity is reduced and ECF pH changes more rapidly in response to Ca-ATPase pumping. The absence of a simple correlation between ECF pH and skeletal Sr/Ca implies that calcification occurred under a range of DIC concentrations, reflecting variations in the respiration and photosynthesis of the coral and symbiotic zooxanthellate in the overlying coral tissues. Our observations have important implications for the use of coral skeletons as indicators of palaeo-ocean pH.     

Acidic compounds in biodegraded petroleum

Twelve oil samples have been characterised by titration, FT-IR and chromatographic analysis to determine the differences between the organic acid composition of biodegraded and non-biodegraded oils. The biodegraded oils have higher total acid and total base contents, both by titration and extraction. The molecular weight ranges of the extracted acids are lowest in the biodegraded oils, and the equivalent weight calculations indicate a dominance of multi-functional molecules. Gel permeation chromatography gives a molecular weight range with most of the molecules between 300 and 500 g/mol. FT-IR shows that the extracted acids from biodegraded oils are more carboxylic and aliphatic while the non-degraded oils are more phenolic. Molecular analysis of the derivatised extracts give UCM envelopes for biodegraded oils, and no molecular identification. The results indicate that the acidic constituents in biodegraded oils are a product of the biodegradation, as the composition is very different from the non-biodegraded oils.     

Notes on the origin of inertinite macerals in coals: Observations on the importance of fungi in the origin of macrinite

Macrinite is a, generally, rare inertinite maceral, often incorporating remnants and fragments of other macerals, including vitrinite, liptinite, and other inertinite. The associated inertinites include multiple forms of funginite. Funginite is also commonly found in association with vitrinite of slightly elevated reflectance and with degraded varieties of vitrinite. Together with the highly degraded macrinite, the latter two associations are here inferred to be part of a continuum of fungal and microbial degradation of peat. In any case, the origin of some macrinite is potentially distinct from that of inertinite generated by fire.     

Palaeoenvironmental records from fossil corals: The effects of submarine diagenesis on temperature and climate estimates

The geochemistry of coral skeletons may reflect seawater conditions at the time of deposition and the analysis of fossil skeletons offers a method to reconstruct past climate. However the precipitation of cements in the primary coral skeleton during diagenesis may significantly affect bulk skeletal geochemistry. We used secondary ion mass spectrometry (SIMS) to measure Sr, Mg, B, U and Ba concentrations in primary coral aragonite and aragonite and calcite cements in fossil Porites corals from submerged reefs around the Hawaiian Islands. Cement and primary coral geochemistry were significantly different in all corals. We estimate the effects of cement inclusion on climate estimates from drilled coral samples, which combine cements and primary coral aragonite. Secondary 1% calcite or ∼2% aragonite cement contamination significantly affects Sr/Ca SST estimates by +1 °C and −0.4 to −0.9 °C, respectively. Cement inclusion also significantly affects Mg/Ca, B/Ca and U/Ca SST estimates in some corals. X-ray diffraction (XRD) will not detect secondary aragonite cements and significant calcite contamination may be below the limit of detection (∼1%) of the technique. Thorough petrographic examination of fossils is therefore essential to confirm that they are pristine before bulk drilled samples are analysed. To confirm that the geochemistry of the original coral structures is not affected by the precipitation of cements in adjacent pore spaces we analysed the primary coral aragonite in cemented and uncemented areas of the skeleton. Sr/Ca, B/Ca and U/Ca of primary coral aragonite is not affected by the presence of cements in adjacent interskeletal pore spaces i.e. the coral structures maintain their original composition and selective SIMS analysis of these structures offers a route to the reconstruction of accurate SSTs from altered coral skeletons. However, Mg/Ca and Ba/Ca of primary coral aragonite are significantly higher in parts of skeletons infilled with high Mg calcite cement. We hypothesise this reflects cement infilling of intraskeletal pore spaces in the primary coral structure.     

Strontium in coral aragonite: 1. Characterization of Sr coordination by extended absorption X-ray fine structure

Aragonite was analyzed from Porites lobata, Pavona gigantea, Pavona clavus, and Montastrea annularis corals by Sr K-edge extended absorption X-ray fine structure (EXAFS) and compared with aragonite, strontianite, and mechanically mixed standards. Bulk analyses were performed and data compared with equivalent micro-EXAFS analyses on small (∼400 μm³) analytical volumes with a microfocused X-ray beam. As a result of the architecture of the coral skeleton, the crystals within the microanalytical volume are not randomly oriented, and the microanalytical X-ray absorption spectra show orientational dependence. However, refinement of bulk and microanalytical data provided indistinguishable interatomic distances and thermal vibration parameters in the third shell (indicative of Sr speciation). The Sr K-edge EXAFS of all the coral samples refine, within error, to an ideally substituted Sr in aragonite, in contrast to previous studies, in which significant strontianite was reported. Some samples from that study were also analyzed here. Strontianite may be less widely distributed in corals than previously thought.     

Stress–strain behavior of cement-improved clays: testing and modeling

The results of a series of laboratory tests on unimproved and cement-improved specimens of two clays are presented, and the ability of a bounding surface elastoplastic constitutive model to predict the observed behavior is investigated. The results of the oedometer, triaxial compression, extension, and cyclic shear tests demonstrated that the unimproved soil behavior is similar to that of soft clays. Cement-improved specimens exhibited peak/residual behavior and dilation, as well as higher strength and stiffness over unimproved samples in triaxial compression. Two methods of accounting for the artificial overconsolidation effect created by cement improvement are detailed. The apparent preconsolidation pressure method is considerably easier to use, but the fitted OCR method gave better results over varied levels of confining stresses. While the bounding surface model predicted the monotonic behavior of unimproved soil very well, the predictions made for cyclic behavior and for improved soils were only of limited success.