Desiccation tolerance ofEurypanopeus depressus (smith) (Decapoda: Xanthidae) and the exploitation of microhabitat

Investigations into zonation of estuarine invertebrates often indicate that animals living higher in the intertidal region have greater tolerance to effects of aerial exposure. Desiccation tolerances ofEurypanopeus depressus, a xanthid mud crab, were measured in the laboratory for both intertidal and subtidal populations to determine whether intertidal distribution is the result of either increased physiological resistance to drying or other factors. Initially, both populations had a similar percentage of body weight due to water, and at time of death both had lost a similar percentage of water. Desiccation tolerance increased exponentially with size. In laboratory experiments,E. depressus appears very susceptible to desiccation stress with loss of tactile response occurring at 30% depletion of body water. This crab may be able to avoid desiccation and survive in the intertidal zone by remaining in the shelter and moisture of oyster shells and mud at low tide. However,E. depressus may not be limited strictly by physical factors of its environment. Biotic factors such as behavior leading to predator avoidance are possibly more important components in limiting distribution.     

Salinity stress in harpacticoid copepods

Three species of intertidal harpacticoid copepods,Tigriopus japonicus, Tachidius brevicornis andTisbe sp., were tested for their response to salinities ranging from 0‰ to 210‰. At 90‰Tigriopus became dormant, but could be reanimated if placed in 30‰ seawater within 18 hours.Tachidius became dormant at 60‰ but could also be revived if placed in 30‰ seawater.Tisbe died shortly after an exposure to seawater of 45‰. Death was brought about inTigriopus andTachidius by salinities of 150‰. Naupliar, copepodite, and adult stages ofTigriopus withstood the salinities equally well, while egg sacs could tolerate five times the length of exposure of these stages. The respiratory rate ofTigriopus was 3.76 (±1.32) μl 0₂ hr^?1 for active adults and 0.03 (±0.01) nl 0₂ hr^?1 mg dry wt^?1 for adults in the dormant state. The duration of dormancy, with successful revival, appears to be limited to the time before the loss of the vital water content of the tissues due to the high osmotic pressure. The ability to enter dormancy in times of stress may have high survival value to some intertidal copepods.     

Upper temperature tolerance of spot,Leiostomus xanthurus,from the cape Fear River estuary,North Carolina

The temperature tolerance and resistance times of postlarval (<25 mm SL) and small juvenile spot,Leiostomus xanthurus, from the Cape Fear Estuary, North Carolina were tested in the laboratory. Critical thermal maximum techniques were used to determine first equilibrium loss (FEL) and critical thermal maximum (CTM) end points and thermal shock methods were used to determine 96-h upper incipient lethal temperatures (LT₅₀). Acclimation temperatures ranged from 10 to 35°C and acclimation salinities were 10, 20 and 30‰. A quadratics model was fit to the CTM and FEL data; r² values were 0.924 and 0.928 respectively. Acclimation salinity, estimated weight, acclimation salinity by acclimation temperature interaction and acclimation temperature by estimated weight interaction were the significant components of the CTM model. Predicted CTM values ranged from 30°C at 10 °C and 30‰ acclimation to just over 40°C at 30 °C and 30‰ acclimation. Acclimation temperature, acclimation temperature squared, estimated weight and acclimation temperatures by estimated weight interaction were the significant components of the FEL model. Predicted FEL values ranged from around 28°C at 10°C and 10‰ acclimation to about 39°C at 30°C and 30‰ acclimation. The 96-h LT₅₀ values of spot acclimated to 20‰ increased linearly with acclimation temperature to 25°C. From about 25 to 35°C, LT₅₀ values increased very little with acclimation temperature. The ultimate upper incipient lethal temperature of postlarval and small juvenile spot was estimated at 35.2°C. Increased salinity increased resistance time but decreased LT₅₀ estimates. Thermal shock tests were better for predicting the effects of thermal addition than were CTM tests.     

Low temperature basalt alteration by sea water: an experimental study at 70°C and 150°C

Basaltic glass and diabase were reacted with seawater at 70°C at 1 bar and 150°C at 500 bars to determine fluid composition and alteration mineralogy. All experiments were performed at a water/ rock mass ratio of 10.The changes in seawater chemistry depended on temperature and crystallinity of the basalt. The experiment at 70°C produced a slight but continuous loss of Mg, Na and K and enrichment of Ca and SiO₂ in the seawater while pH decreased slowly. At 150°C, in contrast, Mg and SO₄ were quickly and quantitatively removed while Ca, SiO₂, Na, K, Fe, Mn and Ba were added to the seawater. pH rose to values between 5.5 and 6.5 after an initial drop to lower values. Basalt glass reacted more extensively at 150°C than diabase.Smectite was the major alteration product (iron-rich saponite) at 150°C for both the glass and diabase experiments. Smectite from the diabase experiment was well crystallized while that from the glass experiment was poorly crystallized. The smectites are similar to smectites found in altered oceanic ophiolitic basalts.     

The effect of temperature and food density on survival and growth of Menidia peninsulae larvae (Pisces: Atherinidae)

Day of hatch tidewater silversides, Menidia peninsulae, were stocked at 5 fish per liter in 3 1 of seawater at 30‰ and raised for 16 days at 20°, 25° and 30 °C. Food organisms (Brachionus sp. or Artemia nauplii) were maintained at 500, 1,000, 5,000 or 10,000 organisms per 1. The influence of food density on growth of larval M. peninsulae was temperature dependent. At 20 °C, there was no difference in final size of fish based on food densities. But at 25° and 30 °C there was an increase in final body size as food density increased. There were no significant differences in survival among food densities in tests at 20°, 25° or 30 °C. However, for any given temperature and food density, the number of survivors in a replicate affected the final size attained. Optimal culture condition for larval M. peninsulae, considering both survival and growth was determined to be 5,000 food organisms per 1 at 25 °C.     

Kinetics of biodegradation of diesel fuel by enriched microbial consortia from polluted soils

Three microbial consortia were isolated from three polluted soils located at an oil refinery and acclimated to grow on diesel fuel as the sole carbon source. Batch experiments were then conducted with the three consortia to study the kinetics of diesel biodegradation. The effects of temperature (25, 30 and 35?°C) and diesel concentration (0.5, 1 and 3?%) on the biodegradation of diesel were analysed. Several species were identified in the acclimated microbial consortia, and some of them appeared in more than one consortium. Thermal inhibition was observed at 35?°C. In the rest of experiments, over 80?% of the substrate was degraded after 40?h of treatment. These results proved the good feasibility of using the polluted sites as sources of mixed consortia for hydrocarbon degradation. However, diesel degradation efficiencies and rates were very similar, suggesting that the acclimation process produced mixed consortia with very similar characteristics; in this context, origin of the soil sample was not a decisive factor. A simple Monod-type kinetic model was used to simulate the biodegradation process, and accurate results were obtained. The ?? _max values were between 0.17 and 0.34?h^?1. The results of this study revealed that the consortia can function at high concentrations of hydrocarbons without any sign of growth inhibition, which is important for the design of bioreactors for wastewater treatment with high concentrations of fuel.     

Between-Population Differences in Multi-stressor Tolerance During Embryo Development in the American Horseshoe Crab, <Emphasis Type="Italic">Limulus polyphemus</Emphasis>

The American horseshoe crab, Limulus polyphemus, is found along the Atlantic and Gulf of Mexico coasts in genetically isolated populations. Eggs are laid in shoreline beaches that expose developing embryos to combinations of environmental stressors. Whether populations of L. polyphemus differ in multi-stressor tolerance had never been tested. We assessed the multi-stressor tolerance of L. polyphemus embryos from a population in Delaware Bay (DE) and determined whether these differed from the multi-stressor tolerance of embryos from a more southerly Florida Gulf Coast (FGC) population. We monitored the field sediment temperatures and determined multi-stressor tolerance of DE embryos, then compared these to published data for FGC embryos. For multi-stressor tolerance, we assessed development success of embryos in 2-week exposures to 36 full-factorial combinations of temperature (20, 25, 30, 35 °C), salinity (5, 15, and 34 ppt), and ambient O₂ (5, 13, and 21% O₂), followed by 2 weeks in recovery conditions. Sediment temperatures in the DE site ranged from 9.5 to 46 °C, with extended periods exceeding 35 °C. Development success was similar between the DE and FGC populations in 14 of 26 multi-stressor combinations. The DE embryos were generally more successful in conditions that included high temperature or moderate hyposalinity, whereas the FGC embryos were generally more successful in conditions that included extreme hyposalinity. This suggests that although multi-stressor tolerances are generally similar between the two populations, specific differences exist that correlate more with differences in nest microenvironment than latitude.     

Submarine metamorphism of gabbros from the Mid-Cayman rise: An oxygen isotopic study

Oxygen isotopic compositions of minerals in 22 samples of submarine gabbros were determined. The gabbros were collected using the submersible Alvin from the 700 m vertical section of the rift-valley wall of the Mid-Cayman spreading center. Our study indicates that in the Mid-Cayman Rise seawater barely reached the bottom of the plutonic layer. Abundant seawater penetration (water/rock mass ratio > 1) was limited to the upper part of the plutonic layer. From the observed oxygen isotopic compositions of coexisting minerals, and from the experimental and empirical determinations of equilibrium fractionation of oxygen isotopes for mineral-water, and mineral-mineral pairs, we show the following: (1) pyroxene and olivine did not exchange oxygen with seawater, (2) plagioclase is in isotopic disequilibrium with pyroxene; (3) the rate of oxygen exchange in plagioclase was not slowed by the absence of cation exchange; (4) plagioclase and amphibole have exchanged oxygen with seawater or isotopically modified seawater (δ¹⁸O ≤ 3%.); and (5) amphibole has exchanged or acquired (during formation) hydrogen from seawater at 380°C ≤ T ≤ 600°C. The decrease in extent of isotopic exchange of plagioclase and the decrease in amphibole abundance with depth indicate that seawater flux decreased rapidly with depth (water/rock mass ratio falling from 1.7 to 0.2 over a 300 m interval).     

Water release patterns of heated speleothem calcite and hydrogen isotope composition of fluid inclusions

Speleothem fluid inclusions are a potential paleo-precipitation proxy to reconstruct past rainwater isotopic composition (δ¹⁸O, δD). To get a better insight in the extraction of inclusion water from heated speleothem calcite, we monitored the water released from crushed and uncrushed speleothem calcite, heated to 900 °C at a rate of 300 °C/h, with a quadrupole mass spectrometer. Crushed calcite released water in three not well individualised peaks between 25 and 360 °C, 360 and 650 °C and between 650 and 800 °C while uncrushed calcite released water in two distinct temperature intervals: between 25 and 550 °C and between 550 and 900 °C.Water from two speleothems from the Han-sur-Lesse cave was recovered using three different techniques: i) the crushing and heating to 360 °C technique, ii) the decrepitation by heating to 550 °C and iii) the decomposition by heating to 900 °C technique. Measurements of the δD of water recovered by the decomposition of Han-sur-Lesse calcite heated to 900 °C did not show a 20 to 30‰ offset as found by previous authors. However a difference of 7‰ was observed between water released before and after decomposition of the calcite. Water recovery from the Han-sur-Lesse samples suggests that a simple heating technique (up to 550 °C) without crushing could both (a) recover water with δD representative of that of the drip water and (b) double the water yield as compared to the crushing and heating method.Our study warns for possible contamination of the recovered inclusion water with hydration water of lime, responsible for the recovery of water with very negative δD values.     

Solubility of corundum in supercritical water

Isothermal (670–700°C) solubility of corundum in supercritical water, within the stability range of corundum as a phase of the system Al₂O₃-H₂O, has been determined by the weight loss method. Experiments were performed in the pressure range 2.5 to 6 kbar in cold seal hydrothermal equipment at 670 ± 5°C using gold tubing. The overall uncertainty of the solubility values obtained was 8%. Experiments in the pressure range 10 to 20 kbar were performed in a piston cylinder apparatus at 700°C using sealed gold capsules held by supporting steel containers. The overall uncertainty of the solubility values obtained was estimated to be 10%.All data could be fitted by the linear equation S_[ppmAl2O3] = ?12.37 + 7.24 · p[_kbar] with correlation coefficient r = 0.9963. Separate fits of hydrothermal and piston cylinder results yielded a small difference between the two data sets, which is due rather to the experimental uncertainty than to the small temperature difference.     

Seawater sulfate reduction and sulfur isotope fractionation in basaltic systems: Interaction of seawater with fayalite and magnetite at 200–350°C

Sulfate reduction during seawater reaction with fayalite and with magnetite was rapid at 350°C, producing equilibrium assemblages of talc-pyrite-hematite-magnetite at low water/rock ratios and talc-pyrite-hematite-anhydrite at higher water/rock ratios. At 250°C, seawater reacting with fayalite produced detectable amounts of dissolved H₂S, but extent of reaction of solid phases was minor after 150 days. At 200°C, dissolved H₂S was not detected, even after 219 days, but mass balance calculations suggest a small amount of pyrite may have formed. Reaction stoichiometry indicates that sulfate reduction requires large amounts of H⁺, which, in subseafloor hydrothermal systems is provided by Mg metasomatism. Seawater contains sufficient Mg to supply all the H⁺ necessary for quantitative reduction of seawater sulfate.Systematics of sulfur isotopes in the 250 and 350°C experiments indicate that isotopic equilibrium is reached, and can be modeled as a Rayleigh distillation process. Isotopic composition of hydrothermally produced H₂S in natural systems is strongly dependent upon the seawater/basalt ratio in the geothermal system, which controls the relative sulfide contributions from the two important sulfur sources, seawater sulfate and sulfide phases in basalt. Anhydrite precipitation during geothermal heating severely limits sulfate ingress into high temperature interaction zones. Quantitative sulfate reduction can thus be accomplished without producing strongly oxidized rocks and resultant sulfide sulfur isotope values represent a mixture of seawater and basaltic sulfur.     

Biogeochemical implications of the isotopic equilibrium fractionation factor between the oxygen atoms of acetone and water

Carbonyl oxygens of organic molecules undergo isotopic exchange with water during reversible hydration reactions. The equilibrium isotopic fractionation factors between the carbonyl oxygen of acetone and water at 15°, 25°, and 35°C are 1.028, 1.028, and 1.026 respectively. The differences between the δ¹⁸O values of the carbonyl oxygen of acetone and of the water with which it is in equilibrium are similar to the differences that have been observed between the δ¹⁸O values of cellulose and the water used in its synthesis by a variety of aquatic plants and animals. Additionally, the identity of the acetone-water fractionation factors at 15° and 25°C parallels the observation that the difference between the δ¹⁸O values of cellulose and water shows no temperature dependence for individual species of plants grown over the same temperature range. These results are discussed in relation to the proposal that the oxygen isotopic relationship between cellulose and water is established by isotopic exchange occurring during the hydration of carbonyl groups of the intermediates of cellulose synthesis.     

The effect of pressure on the ionization of boric acid in sodium chloride and seawater from molal volume data at 0 and 25°C

The apparent molal volume, φ_V of boric acid, B(OH)₃ and sodium borate, NaB(OH)₄, have been determined in 35%. salinity seawater and 0·725 molal NaCl solutions at 0 and 25°C from precise density measurements. Similar to the behavior of nonelectrolytes and electrolytes in pure water, the φ_V of B(OH)₃ is a linear function of added molality and the φ_V of NaB(OH)₄ is a linear function of the square root of added molarity in seawater and NaCl solutions. The partial molal volumes, $\text{V}\text{?}\text{1}$, of B(OH)₃ and NaB(OH)₄ in seawater and NaCl were determined from the φ_V's by extrapolating to infinite dilution in the medium. The $\text{V}\text{?}\text{1}$ of B(OH)₃ is larger in NaCl and seawater than pure water apparently due to the ability of electrolytes to dehydrate the nonelectrolyte B(OH)₃. The $\text{V}\text{?}\text{1}$ of NaB(OH)₄ in itself, NaCl and seawater is larger than the expected value at 0·725 molal ionic strength due to ion pair formation [Na⁺ + B(OH)₄^? → NaB(OH)₄⁰]. The volume change for the formation of NaB(OH)₄⁰ in itself and NaCl was found to be equal to 29·4 ml mol^?1 at 25°C and 0·725 molal ionic strength. These large $\text{Δ}\text{V}\text{?}\text{1}$'s indicate that at least one water molecule is released when the ion pair is formed [Na⁺ + B(OH)₄^? → H₂O + NaOB(OH)₂⁰]. The observed $\text{V}\text{?}\text{1}$ in seawater and the $\text{Δ}\text{V}\text{?}\text{1}$ (NaB⁰) in water and NaCl were used to estimate $\text{Δ}\text{V}\text{?}\text{1 (MgB}{}^{\mathrm{+}}\text{) = Δ}\text{V}\text{?}\text{1 (CaB}{}^{\mathrm{+}}\text{) = 38·4 ml mol}{}^{\mathrm{?1}}$ for the formation of MgB⁺ and CaB⁺. The volume change for the ionization of B(OH)₃ in NaCl and seawater was determined from the molal volume data. Values of $\text{Δ}\text{V}\text{?}\text{1 = ?29·2 and ?25·9 ml mol}{}^{\mathrm{?1}}$ were found in seawater and $\text{Δ}\text{V}\text{?}\text{1 = ?21·6 and ?26·4}$ in NaCl, respectively, at 0 and 25°C. The effect of pressure on the ionization of B(OH)₃ in NaCl and seawater at 0 and 25°C determined from the volume change is in excellent agreement with direct measurements in artificial seawater (culberson and Pytkowicz, 1968; Disteche and Disteche, 1967) and natural seawater (Culberson and Pytkowicz, 1968).     

Computer simulation of the transformation of natural living matter into kerogen

Thermodynamic simulation of the system living matter (algae, zooplankton, or green plants) + mineral matter (25% carbonates + 75% clay minerals) + standard seawater at temperatures and pressure corresponding to diagenesis indicates that kerogen can be synthesized, together with hydrocarbons and carbon dioxide, in the reaction mix. The removal of CO₂(g) and N₂(g) from the system is favorable for the reaction Δ₁C₂₉₂H₂₈₈O₁₂ (s; H/C = 0.99, O/C = 0.041) → Δ₂C₁₂₈H₆₈O₇ (s; H/C = 0.53, O/C = 0.055) + xСH₄(aq) + yCO₂(aq) + zH₂O, whose constant and stoichiometric coefficients were calculated based on the simulation results. It is demonstrated that a pressure increase is favorable, while a temperature increase is not, for the procedure of this reaction at P-T parameters of diagenesis: log K =–567 (20°C, 35 bar), 1170 (20°C, 200 bar),–1530 (20°C, 60 bar), and +1030 (20°C, 600 bar).     

A novel multiproxy approach to reconstruct the paleoecology of extinct cephalopods

Reconstructing marine paleoenvironments from the skeletal hardparts of nektic organisms is often hampered by their unknown migrational pathways involving different water masses and their corresponding physico-chemical parameters. Despite significant progress over the last years, the reconstruction of migration patterns of extinct ammonoids is difficult because both, vertical and horizontal ones lead to an intricate combination of reconstructed seawater temperatures. Paleonvironmental data retrieved from exceptionally well-preserved lower Albian (Douvilleiceras mammillatum ammonite zone, uppermost CC8a nannofossil zone, 110.5–111.0 Ma) cephalopod shells from Madagascar (Mahajanga Basin, 40–42° southern latitude) are reconstructed based on a novel multi-proxy approach. Here we combine and contrast: (i) nacre tablet-paleobathymetry, (ii) Westermann Morphospace, and (iii) shell isotope geochemistry analysis. Results obtained allow for a robust reconstruction of habitat depth, paleo-seawater temperatures, and paleoecology of extinct cephalopod taxa. The discocone nautiloid Cymatoceras is regarded as vertical migrant with a maximum habitat depth of 250 m and a mean habitat water temperature of 20–21 °C. All three ammonoid taxa (Cleoniceras, Desmoceras, and Eogaudryceras) share a platycone to planorbicone shell shape suggesting a demersal life habit at maximal water depths of 450–500 m and temperatures of 19–21 °C for Cleoniceras and Desmoceras, and the deepest (525 m) and coolest (14 °C) habitat for Eogaudryceras. Circumstantial evidence from benthic mollusk shells from the same stratigraphic interval as well as sedimentological and paleopathological data provide further support for habitat reconstructions. Reconstructed paleotemperatures shown here provide well-constrained evidence for the thermal structure of past oceanic water masses and have significance for Cretaceous paleoceanography in general.     

Competitive interference during the biodegradation of cresols

Phenol and its methylated derivatives, cresol isomers, are hazardous pollutants that are commonly present in various industrial effluents and known to have detrimental effect on aquatic life as well as human health, due to their toxic and carcinogenic nature. It is essential, therefore, to reduce the concentration of these contaminants in industrial effluent to acceptable levels prior to being discharged into the environment. Bacterial cells of the strain Pseudomonas putida, with excellent biodegradation capabilities and high tolerance of cresols, were extracted and immobilized in polyvinyl alcohol (PVA) gel for cresols biodegradation. The biodegradation was carried out at different operating conditions, in both batch and continuous modes, using a cylindrical spouted bed bioreactor. Factors affecting o-cresol and m-cresol degradation were studied in batch experiments, and the results showed that the immobilized bacteria could tolerate cresols concentration up to 200 mg/l. Moreover, the experiments indicated that the biodegradation rate was highly affected by the operating parameters such as pH and temperature, with optimum ranges of 6–8 for pH and 30–35 °C for temperature. However, the optimum conditions were different for each cresol isomer. The potential of P. putida in degrading binary and ternary mixtures of cresols was also examined in the continuous process and compared with single component biodegradation. The experimental results revealed that the biodegradation of o-cresol was highly inhibited by the presence of p-cresol and m-cresol.     

Chemical exchange during hydrothermal alteration of basalt by seawater—II. Experimental results for Fe,Mn, and sulfur species

Fresh mid-ocean ridge basalts of varying crystallinity and an andesite were reacted with seawater and with a Na-K-Ca-Cl solution at 200–500°C and 500–1000 bar in sealed gold capsules. $\text{Water}\text{rock}$ mass ratios of one to three were used and durations ranged from two to twenty months. The concentrations of Fe, Mn, and reduced and oxidized sulfur species in solution reached steady state in most of the experiments at 400–500°C, but not in those at 200–300°. The concentrations of Fe and Mn were a few ppm at 200–300° and increased greatly with temperature between 300 and 500°. The low values at 200–300° are probably related to the uptake of Fe and Mn by smectite at the in situ pH, which was slightly acid at 200° and slightly alkaline at 300°. The quench pH values decreased with increasing temperature above 300°. The only reliable data for the concentration of Zn in solution were obtained at 400°, where values 1–2 ppm were found. Copper was extensively leached from basalt and andesite and was deposited as part of a Cu-Au alloy in the capsule walls or, in some experiments, as chalcopyrite.Reduced sulfur was readily leached from basalt into solution, and was also produced by the reduction of seawater sulfate by ferrous iron derived from the basalts. The proportion of seawater sulfate which was reduced in the experiments with a $\text{water}\text{rock}$ ratio of one varied from 5–10% at 300°C to > 95% at 500°. The rate of sulfate reduction depended on the run temperature, on the crystallinity and initial sulfur content of the rocks used as starting materials, and on the $\text{water}\text{rock}$ ratio. The final concentration of reduced sulfur in solution increased greatly with temperature, and generally exceeded that of Fe on a molal basis.The oxide-sulfide assemblages produced in the experiments resemble those in the basalt-seawater geothermal system at Reykjanes, Iceland, and in hydrothermally altered basalts and gabbros from the oceanic crust; they include pyrite, pyrrhotite. chalcopyrite, hematite, and probably magnetite. The particular assemblage varied systematically with the temperature, rock type, and crystallinity of each run. Anhydrite precipitated in all experiments with seawater, at all temperatures from 200–500°C. However, its persistence to the end of the runs was apparently metastable, as it should have reacted with the final solutions to produce pyrite or pyrrhotite.     

A secondary isotopic reference material of chlorine from selected seawater

A secondary isotopic reference material of chlorine as NaCl collected from a sea water, located at 4°18′N, 161°08′E and collected on October 22, 1994, was prepared using ion exchange technique. The δ³⁷Cl of an NaCl product named ISL 354 was measured to be −0.39±0.05‰ (2σ) related to NIST SRM 975, an isotopic standard reference material with an absolute ³⁷Cl/³⁵Cl ratio of 0.31977. No contamination or isotopic fractionation was observed due to a complete recovery of chlorine and the avoidance of chemical reagents during preparation of ISL 354 from selected seawater. The isotopic composition of chlorine in ISL 354 does not change on long-term storage. So ISL 354 can be used as a secondary isotopic reference material of chlorine.     

Calcite and aragonite saturation States of Kamaran strait surface seawater, Yemen: summer time

Surface seawater samples from Kamaran Strait of Yemen were collected for physical and chemical parameter determinations. This work reports the results of air and surface seawater temperature, salinity, pH, and total alkalinity measurements. The air temperature ranged from 29.9°C to 36.5°C with an average value of 31.5?±?1.5°C, whereas the seawater surface temperature ranged from 34.0°C to 36.0°C with a mean value of 34.5?±?0.5°C. The salinity was observed to be high, ranging from 38.03 to 38.81 with an average value of 38.45?±?0.22. The pH ranged from 7.74 to 8.27 with a mean value of 8.11?±?0.10. The total alkalinity was found to range from 2.3860 to 2.5000 meq L^?1 with an average value of 2.4288?±?0.0351 meq L^?1. The result of the study showed that there was a negative correlation between the pH and surface seawater temperature and salinity. The surface seawater of the Kamaran Strait was found to be several fold supersaturated with respect to calcium carbonate. The measured percent degree of saturation ranged from 454% to 668% with respect to calcite and from 246% to 361% with respect to aragonite. The lowest value of supersaturation with respect to both calcite and aragonite were found in front of as-Salif port, where human and developmental activities are intensively increased. The visual inspection of coral reefs distribution and their intensity were obviously observed in areas of high value of supersaturation with respect to both minerals, high transparency of seawater column, and low human activities. Further studies are needed to investigate the occurrence, distribution, and mineralogy of corals and the effects of physical and chemical parameters upon their growth in the region.     

Hydrogen and oxygen isotope ratios in nodular and bedded cherts

Hydrogen and oxygen isotopic compositions of cherts (δD for hydroxyl hydrogen in the chert, δ¹⁸O for the total oxygen) have been determined for a suite of samples from the central and western United States. When plotted on a δD-δ¹⁸O diagram, Phanerozoic cherts define domains parallel to the meteoric water line which are different for different periods of geologic time. The elongation parallel to the meteoric water line suggests that meteoric waters were involved in the formation of many cherts.The existence of different chert δ-values for different geologic times indicates that once the granular microcrystalline quartz of cherts crystallizes its isotopic composition is preserved with time. An explanation for the change with time of the isotopic composition of cherts involving large changes with time in the isotopic composition of ocean water is unlikely since δ¹⁸O of the ocean would have had to decrease by about 3‰between Carboniferous and Triassic time and then increase about 5%.` from Triassic to Cretaceous time. Such isotopic changes cannot be accounted for by extensive glaciation, sedimentation of hydrous minerals, or input of water from the mantle into the oceans.The variation with time of the chert δ-values can be satisfactorily explained in terms of past climatic temperature fluctuations if the chert-water isotope fractionation with temperature is approximated by 1000 lnα = 3.09 × 10⁶T^?2 – 3.29. Crystallization temperatures so inferred suggest that the average climatic temperatures for the central and western U.S. decreased from about 34 to 20°C through the Paleozoic, increased to 35–40°C in the Triassic, and then decreased through the Mesozoic to Tertiary values of about 17°C. A few data for the Precambrian suggest the possibility that Earth surface temperatures may have reached about 52°C at 1.3 b.y. and about 70°C at 3 b.y.