Seasonal variation in lysosomal destabilization in oysters,Crassostrea virginica

Lysosomal destabilization assays have been used as valuable biomarkers of pollutant exposures in a variety of bivalve and fish species. The responses of oysters, Crassostrea virginica, deployed at and native to various reference and degraded sites were evaluated for lysosomal destabilization during both summer and winter seasons. In both native and deployed oysters, lysosomal destabilization rates tended to be higher during the winter at both reference and polluted sites. There are at least two hypothetical explanations. Greater lysosomal destabilization rates may be related to physiological changes associated with mobilization of nutrient reserves during the winter and gametogenesis. However, lysosomal destabilization in deployed oysters was correlated with tissue metal concentrations. These data also support a second hypothesis that seasonal differences in physico-chemical factors (such as reduced levels of acid volatile sulfides) may increase the bioavailability of metals during the winter so that adverse effects are more pronounced.     

Expression of P-glycoprotein in southeastern oysters, Crassostrea virginica

These studies provide important fundamental information regarding the expression of P-glycoprotein (p-gp) in southeastern oysters (Crassostrea virginica). Using rhodamine transport studies, p-gp activity was detected in newly fertilized embryos. A monoclonal antibody (C219) was used to evaluate p-gp expression in oyster tissues. On the basis of laboratory studies, p-gp expression tended to be higher in gill tissues than mantle tissues, and was generally not related to salinity differences. Seasonal studies were conducted with oysters collected monthly for 1 year from Lighthouse Creek, an unpolluted site. There was a general pattern of higher p-gp expression in the warmer months and lower expression in the colder months. In contrast, total gill protein concentrations decreased during the warmer months and increased during the colder months. These studies indicate that there are seasonal patterns in p-gp expression which may represent an adaptive response to natural stressors associated with summer conditions.     

A study of bernalite,Fe(OH)3, using Mössbauer spectroscopy,optical spectroscopy and transmission electron microscopy

To study the crystal chemistry of bernalite, Fe(OH)₃, and the nature of the octahedral Fe³⁺ environment, Mössbauer spectra were recorded from 80 to 350 K, optical spectra were recorded at room temperature and a sample was studied using transmission electron microscopy. The Mössbauer spectrum of bernalite consists of a single six-line magnetic spectrum at 80 K. A broadened six-line magnetic spectrum with significantly less intensity is observed at higher temperatures, and is attributed to a small fraction of bernalite occurring as small particles. The variation of hyperfine magnetic field data for bulk bernalite with temperature is well described by the Weiss molecular field model with parameters of H ₀ = 55.7±0.3 T and T _N = 427±5K. The centre shift data were fitted to the Debye model with parameters ₀=0.482±0.005 mm/s (relative to -Fe) and _M=492±30 K. The quadrupole shift is near zero at 300 K, and does not vary significantly with temperature. Absorption spectra in the visible and near infrared range show three crystal field bands of Fe³⁺ at 11 300, 16000 and 23 200 cm^-1, giving a crystal field splitting of 14 570 cm^-1 and Racah parameters of B=629 cm^-1 and C=3381 cm^-1. Infrared reflection spectra show two distinct OH-stretching frequencies, which could correspond to two structurally different types of OH groups. A band was also observed at 2250 cm^-1, suggesting the presence of molecular CO₂ in the large cation site. Analytical transmission electron microscopy indicates that Si occurs within the bernalite structure as well as along domain boundaries. Electron diffraction and imaging show that bernalite is polysynthetically twinned along {100} planes with twin domains ranging from 3 to 20 nm in thickness. Results are discussed with respect to the nature of the octahedral Fe³⁺ site, and compared with values for other iron oxides and hydroxides.     

Water solubility in orthopyroxene

The solubility of water in pure enstatite was measured on samples synthesized at 1,100 °C and pressures to 100 kbar. Enstatite crystals were grown under water-saturated conditions from a stoichiometric mixture of high-purity SiO₂ and Mg(OH)₂. Water contents were calculated from polarized FTIR spectra measured on oriented single crystals. The water solubility in orthoenstatite increases with pressure to 867ᆷ ppm H₂O by weight at 75 kbar. At 100 kbar, in the stability field of high-clinoenstatite, a water solubility of 714ᆷ ppm was observed. The water solubility in enstatite at 1,100 °C can be described by the equation c_H2O=Af_H2O exp(-P(V/RT), where f_H2O is water fugacity, A=0.0204 ppm/bar and (V=12.3 cm³/mol. The infrared spectra of the hydrous enstatite crystals show a sharp, intense band at 3,363 cm^-1 and a broad, weaker band at 3,064 cm^-1. Both bands are strongly polarized parallel c. Most likely, pairs of protons attached to non-bridging oxygen atoms substitute for Mg²⁺. In order to investigate the effect of chemical impurities on water solubility in enstatite, an additional series of experiments was carried out with gels doped with Al, B, or Li as starting material. Whereas, the presence of Li and B had no detectable effect on water solubility, the addition of about 1 wt% Al₂O₃ increased water solubility in enstatite from 199 to 1,100 ppm at 1,100°C and 15 kbar. In the infrared spectra of these aluminous samples, additional bands occur in the range from 3,450 to 3,650 cm^-1. Similar bands are also observed in natural, aluminous orthopyroxenes and are most likely caused by protons coupled with Al according to the substitution of Al³⁺+H⁺ for Si⁴⁺. A series of hydrous annealing experiments on a natural, gem-quality aluminous enstatite from Tanzania yielded water solubilities generally consistent with the results from the synthetic model systems. The results presented here imply that pure enstatite has a similar storage capacity for water as olivine; however, aluminous orthopyroxenes in the mantle may dissolve much larger amounts of water comparable with the entire mass of the present hydrosphere. Moreover, the mechanism of aluminum substitution in orthopyroxenes, i.e., the distribution of Al between tetrahedral and octahedral sites, may be a potential probe of water fugacity.     

Water quality variation and clam growth: Is pH really a non-issue in estuaries?

A tandem deployment system was used to critically evaluate relationships between important water chemistry parameters (pH, salinity, dissolved oxygen) and biotic performance based on clam growth. The effects of environmental conditions on growth of juvenile clams,Mercenaria mercenaria, were determined after 7-day field deployments in cages at reference sites from 1998 to 2000. Continuous measurements of the overlying water chemistry parameters were monitored by deploying an in situ water quality instrument (Hydrolab Datasonde) at the same time. While salinity was identified as an important determinant of clam growth over wide salinity ranges (10–35‰), pH was also found to be a very important parameter, especially in low-salinity regimes (<25‰). Average pH measurements ranged from 7.2 to 7.8; minimal pHs ranged from 6.9 to 7.6. The results indicated that when average pH levels fell below 7.5 or minimum pH levels fell below 7.2, growth rates were <50% that of clams deployed under higher pH conditions. Estuarine systems are generally perceived as being well-buffered so pH is frequently assumed to be unimportant, but our results suggest that pH levels can decline in estuarine systems to levels that can adversely affect biological responses. The potential impacts on biological resources of even moderate decreases in pH, particularly in systems that naturally tend to have lower pH conditions, may be more important than previously realized.     

The influence of the fluid phase composition on the solidus temperatures in the haplogranite system NaAlSi3O8-KAlSi3O8-SiO2-H2O-CO2

The solidus temperatures in the haplogranite-system NaAlSi₃O₈-KAlSi₃O₈-SiO₂-H₂O-CO₂ have been determined up to 15 kbar for a constant molar ratio of sodium to potassium of 11 and for fluid compositions ranging from pure water to pure carbon dioxide. The data for the water-saturated solidus are virtually identical with those of previous studies. At constant pressure, the solidus curve as a function of the fluid phase composition exhibits a point of inflection in the range of the water-rich compositions. This phenomenon is attributed to chemical interactions between the CO₂ and the H₂O in the silicate melt. The point of inflection disappears if the CO₂ in the gas phase is replaced by molecular nitrogen. The CO₂-saturated solidi have been measured at 2 and 5 kbars. The data at 5 kbar indicate a melting point depression in the order of 40° C compared to the dry solidus of Huang and Wyllie (1975). The experimental data can be used to estimate the melting temperatures of common quartz and feldspar bearing crustal rocks under the conditions of granulite facies metamorphism. Since for most fluid phase compositions, the solidus curves are very steep in the P, T-diagram, the beginning of melting is nearly exclusively determined by the fluid composition and almost independent of pressure between about 2 and more than 10 kbar. Therefore, the onset of partial melting in quartz and feldspar containing rocks under granulite facies conditions can be used to estimate the composition of a coexisting H₂O-CO₂ fluid phase if geothermometric data are available. The temperature range between the beginning of granulite facies metamorphism and the initiation of melting expands with increasing carbon dioxide content in the H₂O-CO₂ fluid phase. At a CO₂ molar fraction of 0.9, this range extends from about 600° C to 900° C and is almost independent of pressure.     

ULYSSES observations of energetic particle acceleration and the superposed CME and CIR events of November 1992

During November 1992, a series of forward and reverse shocks passed the ULYSSES spacecraft. Spectral and anisotropy measurements are reported for protons and alpha particles between 0.28 and 6 MeV observed by the Energetic Particle Composition Experiment, data recorded by the Magnetometer Experiment and the high-energy (2.7-300 MeV) proton data from the Kiel Electron Telescope. An analysis of energetic particle, plasma and magnetometer data from ULYSSES has allowed a unique study of the corresponding arrival of fare particles, particles within a corotating interaction region and particles transported with a coronal mass ejection. We present an analysis of these data in terms of possible diffusive shock acceleration but conclude that this is likely to be incompatible with the short transit time of the particles. Shock drift acceleration of particles with energies 0.3 MeV/nucleon or solar acceleration followed by particle trapping behind the shock front are alternative possibilities.     

The structure of sodium tetrasilicate glass from neutron diffraction, reverse Monte Carlo simulations and Raman spectroscopy

The reverse Monte Carlo (RMC) method was used for modelling the three-dimensional structure of sodium tetrasilicate glass (Na₂Si₄O₉, NS4). Neutron diffraction data over a large momentum transfer range and nuclear magnetic resonance results (Q-species distribution) as well as chemical bonding considerations have been used to constrain the RMC simulations. Very good agreement with the experimental structure factor was achieved. The three-dimensional model is analysed in terms of partial pair distribution functions, bond-angle distributions, short-range order (SRO) clusters and ring statistics. The average Si–O–Si bridging angle is different for the different Qⁱ–Q^j units. The effect of different Q species on the network connectivity is analysed by comparison with statistical SRO distributions. While the Q² species are randomly distributed, a high preference for the formation of Q⁴–Q⁴ units in three-membered rings is found. This explains why during the initial stages of hydration of NS4 glass, Si–OH groups are preferentially formed by breaking Q⁴–Q⁴ linkages. The RMC model also provides an independent test for the assignment of bands in the Si–O stretching region of the Raman spectrum. It is shown that the bands at about 1050 and 1100 cm⁻¹ are probably due to Q³ units surrounded by different numbers of Q⁴ units. Received: 7 April 1997 / Revised, accepted: 5 July 1997     

西天山喇嘛苏铜矿成矿斑岩的岩石学、地球化学特征及成因探讨

位于西天山别珍套-科古琴晚古生代岛弧西段的喇嘛苏铜矿床是区内最大的铜矿床,与成矿作用有着密切关系的斑岩体为英云闪长斑岩、花岗闪长斑岩,是同源岩浆分异演化的产物,且花岗闪长斑岩可能属于岩浆演化晚期的产物。本区成矿斑岩的主量、微量元素和Sr-Nd同位素地球化学特征表明,其富集大离子亲石元素,而相对亏损高场强元素,出现了较为明显的Ta、Nb负异常,初始锶同位素ISr和εNd(t=390Ma)值分别为0.7072～0.7076和-0.32～0.17,显示壳幔混合源的特征,利用Sr和Nd同位素估算其源区物质约有50%来源于地壳。岩石地球化学特征指示了其为典型钙碱性火山弧花岗岩,暗示其形成于大陆弧环境。结合区域地质背景,推测本区成矿斑岩是在洋壳俯冲作用下发生部分熔融,交代原先的地幔楔,并混合了部分下地壳的物质,经历分离结晶作用的产物,其形成可能与晚古生代准噶尔洋板块向南的俯冲作用有关。结合东西天山的成矿斑岩的地球化学特征对比研究,岩浆源区的差别可能导致不同类型斑岩型矿床的形成,斑岩型铜矿床的形成较斑岩型钼矿床可能有更少的地壳物质贡献。     

Relationships between molecular bacterial diversity and chemistry of groundwater in the Wairarapa Valley,New Zealand

Groundwater plays an important role in New Zealand water supplies and hence monitoring activities are conducted regularly. Most monitoring programmes aim to evaluate groundwater chemistry and almost completely overlook the microbial component in this ecosystem. In our present study, the bacterial community structure of groundwater in the Wairarapa Valley was examined using the terminal restriction fragment length polymorphism (T-RFLP), and relationships between bacterial community structure and groundwater chemistry, aquifer confinement and groundwater usage were explored. In addition, the results from this study were compared with a previous T-RFLP survey of the same area in an attempt to detect changes in bacterial community structure over time. The data obtained suggested that bacterial community structure was related to groundwater chemistry, especially to redox conditions. Species composition showed minimal variation over time if groundwater chemistry remained unchanged. These findings reflect the potential of using bacterial communities as biological indicators to evaluate the health of groundwater ecosystems. We suggest that it is important to include this type of broad bacterial diversity assessment criteria into regular groundwater monitoring activities.