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Electron microscope study of Sarcocystis sp

Sarcocystis sp. obtained from wild populations of grackles, Quiscalus quiscula (Linn.), were examined to clarify the effect of the parasite on the host. Electron micrographs are presented to show areas of muscle destruction adjacent to the parasite which appear to be mechanically produced by the parasite. The microtubules within the villus-like projections of the cyst suggest that their possible function is absorptive and/or conductive with regard to the production of a toxin or the conveyance of nutritive material to the developing cells. The proposed function of submembranous filaments and their relation to the conoid is discussed. Similarities in the ultrastructure to Toxoplasma and other protozoa tend to negate the relegation of Sarcocystis to the fungi and further emphasize its protozoan nature.

Experimental Parasitology↗

Systematic variation of rare-earth elements in cerium-earth minerals

In a continuation of a study reported previously, rare-earth elements and thorium have been determined in monazite, allanite, cerite, bastnaesite, and a number of miscellaneous cerium-earth minerals. A quantity called sigma (∑), which is the sum of the atomic percentages of La, Ce, and Pr, is proposed as an index of composition of all cerium-earth minerals with respect to the rare-earth elements. The value of ∑ for all of the minerals analysed falls between 58 and 92 atomic per cent. Monazites, allanites, and cerites cover the entire observed range, whereas bastnaesites are sharply restricted to the range between 80 and 92 atomic per cent. The minimum value of ∑ for a cerium-earth mineral corresponds to the smallest possible unit-cell size of the mineral. In monazite, this structurally controlled minimum value of ∑ is estimated to be around 30 atomic per cent. Neodymium, because of its abundance, and yttrium, because of its small size, have dominant roles in contraction of the structure. In the other direction, the limit of variation in composition will be reached when lanthanum becomes the sole rare-earth element in a cerium-earth mineral. Cerium-earth minerals from alkalic rocks are all characterized by values of ∑ greater than 80 atomic per cent, indicating that the processes that formed these rocks were unusually efficient in fractionating the rare-earth elements—efficient in the sense that a highly selected assemblage is produced without eliminating the bulk of these elements. Analyses of inner and outer parts of two large crystals of monazite from different deposits show no difference in ∑ in one crystal and a slightly smaller value of ∑ in the outer part of the other crystal compared to the inner part. The ∑ of monazites from pegmatites that intrude genetically related granitic rocks in North Carolina is found to be either higher or lower than the ∑ of monazites in the intruded host rock. These results indicate that the fractionation of the rare-earth elements is not a simple unidirectional process. When a cerium-earth mineral undergoes replacement, its rare-earth elements may be fractionated into two parts, one forming a new mineral with ∑ that is smaller, and the other a second new mineral with ∑ that is larger than that of the original mineral. The complete analysis of a cerium-earth mineral to determine its ∑ is time consuming. The discovery of a direct relationship between ∑ and the Ce/(Nd + Y) atomic ratio in cerium earth minerals allows a rapid determination of ∑ from spectrograms obtained in a previously described method for determining thorium in these minerals.

Geochimica et Cosmochimica Acta↗

Dissociation constants of KSO 4 - from 10°-50°C

A cell without liquid junction was used to obtain dissociation constants for the reaction: KSO 4 − = K + + SO 4 2− . At 10°, 25°, 38° and 50°C, values for K diss KSO 4 − are, respectively, 0.19 5 , 0.14 2 , 0.11 7 , and 0.09 5 . At 25°C, , and values for the KSO 4 − ion are −245.96 and −274.02 kcal mole −1 , and S ° is +42.3 cal mole −1 deg −1 .

Geochimica et Cosmochimica Acta↗

Simultaneous flow of water and solutes through geological membranes-I. Experimental investigation

The relative retardation by geological membranes of cations and anions generally present in subsurface waters was investigated using a high pressure and high temperature ‘filtration cell’. The solutions were forced through different clays and a disaggregated shale subjected to compaction pressures up to 9500 psi and to temperatures from 20 to 70°C. The overall efficiences measured increased with increase of exchange capacity of the material used and with decrease in concentration of the input solution. The efficiency of a given membrane increased with increasing compaction pressure but decreased slightly at higher temperatures for solutions of the same ionic concentration. The results further show that geological membranes are specific for different dissolved species. The retardation sequences varied depending on the material used and on experimental conditions. The sequences for monovalent and divalent cations at laboratory temperatures were generally as follows: Li < Na < NH 3 < K < Rb < Cs Mg < Ca < Sr < Ba. The sequences for anions at room temperature were variable, but at 70°C, the sequence was: HCO 3 < I < B < SO 4 < Cl < Br. Monovalent cations contrary to some field data were generally retarded with respect to divalent cations. The differences in the filtration ratios among the divalent cations were smaller than those between the monovalent cations. The passage rate of B, HCO 3 , I and NH 3 was greatly increased at 70°C.

Geochimica et Cosmochimica Acta↗

Degradation of carbohydrates and lignins in buried woods

Spruce, alder, and oak woods deposited in coastal sediments were characterized versus their modern counterparts by quantification of individual neutral sugars and lignin-derived phenols as well as by scanning electron microscopy, 13 C NMR, and elemental analysis. The buried spruce wood from a 2500 yr old deposit was unaltered whereas an alder wood from the same horizon and an oak wood from an open ocean sediment were profoundly degraded. Individual sugar and lignin phenol analyses indicate that at least 90 and 98 wt% of the initial total polysaccharides in the buried alder and oak woods, respectively, have been degraded along with 15–25 wt% of the lignin. At least 75% of the degraded biopolymer has been physically lost from these samples. This evidence is supported by the SEM, 13 C NMR and elemental analyses, all of which indicate selective loss of the carbohydrate moiety. The following order of stability was observed for the major biochemical constituents of both buried hardwoods: vanillyl and p- hydroxyl "> p-hydroxyl lignin structural units > syringyl and lignin structural units > pectin > α-cellulose > hemicellulose. This sequence can be explained by selective preservation of the compound middle lamella regions of the wood cell walls. The magnitude and selectivity of the indicated diagenetic reactions are sufficient to cause major changes in the chemical compositions of wood-rich sedimentary organic mixtures and to provide a potentially large in situ nutrient source.

Geochimica et Cosmochimica Acta↗

Kinetic and thermodynamic factors controlling the distribution of SO32- and Na+ in calcites and selected aragonites

Significant amounts of SO 4 2− , Na + , and OH − are incorporated in marine biogenic calcites. Biogenic high Mg-calcites average about 1 mole percent SO 4 2− . Aragonites and most biogenic low Mg-calcites contain significant amounts of Na + , but very low concentrations of SO 4 2− . The SO 4 2− content of non-biogenic calcites and aragonites investigated was below 100 ppm. The presence of Na + and SO 4 2− increases the unit cell size of calcites. The solid-solutions show a solubility minimum at about 0.5 mole percent SO 4 2− beyond which the solubility rapidly increases. The solubility product of calcites containing 3 mole percent SO 4 2− is the same as that of aragonite. Na + appears to have very little effect on the solubility product of calcites. The amounts of Na + and SO 4 2− incorporated in calcites vary as a function of the rate of crystal growth. The variation of the distribution coefficient ( D "> D ) of SO 4 2− in calcite at 25.0°C and 0.50 molal NaCl is described by the equation D = k 0 + k 1 R "> D = k 0 + k 1 R where k 0 "> k 0 and k 1 "> k 1 are constants equal to 6.16 &#xD7; 10 &#x2212;6 "> 6.16 × 10 −6 and 3.941 &#xD7; 10 &#x2212;6 "> 3.941 × 10 −6 , respectively, and R "> R is the rate of crystal growth of calcite in mg·min −1 ·g −1 of seed. The data on Na + are consistent with the hypothesis that a significant amount of Na + occupies interstitial positions in the calcite structure. The distribution of Na + follows a Freundlich isotherm and not the Berthelot-Nernst distribution law. The numerical value of the Na + distribution coefficient in calcite is probably dependent on the number of defects in the calcite structure. The Na + contents of calcites are not very accurate indicators of environmental salinities.

Geochimica et Cosmochimica Acta↗

Bacterial ethane formation from reduced, ethylated sulfur compounds in anoxic sediments

Trace levels of ethane were produced biologically in anoxic sediment slurries from five chemically different aquatic environments. Gases from these locations displayed biogenic characteristics, having 12 C-enriched values of δ 13 CH 4 (−62 to −86%.), δ 13 C 2 H 6 (−35 to −55%.) and high ratios (720 to 140,000) of CH 4 [C 2 H 6 + C 3 H 8 ] "> CH4[C2H6+ C3H8] . Endogenous production of ethane by slurries was inhibited by autoclaving or by addition of the inhibitor of methanogenic bacteria, 2-bromoethanesulfonic acid (BES). Ethane formation was stimulated markedly by ethanethiol (ESH), and, to a lesser extent, by diethylsulfide (DES). Formation of methane and ethane in ESH- or DES-amended slurries was blocked by BES. Experiments showed that ethionine (or an analogous compound) could be a precursor of ESH. Ethylamine or ethanol additions to slurries caused only a minor stimulation of ethane formation. Similarly, propanethiol additions resulted in only a minor enhancement of propane formation. Cell suspensions of a methyltrophic methanogen produced traces of ethane when incubated in the presence of DES, although the organism did not grow on this compound. These results indicate that methanogenic bacteria produce ethane from the traces of ethylated sulfur compounds present in recent sediments. Preliminary estimates of stable carbon isotope fractionation associated with sediment methane formation from dimethylsulfide was about 40%., while ethane formation from DES and ESH was only 4. 6 and 6.5%., respectively.

Geochimica et Cosmochimica Acta↗

Reduction of aqueous transition metal species on the surfaces of Fe(II)-containing oxides

Experimental studies demonstrate that structural Fe(II) in magnetite and ilmenite heterogeneously reduce aqueous ferric, cupric, vanadate, and chromate ions at the oxide surfaces over a pH range of 1–7 at 25°C. For an aqueous transition metal m , such reactions are 3 [ Fe 2 + Fe 2 3 + ] O 4 (magnetite) + 2 / n m z &#x2192; 4 [ Fe 2 3 + ] O 3 (magnetite) + Fe 2 + + 2 / n m z &#x2212; n "> 3[Fe2+Fe23+]O4(magnetite)+2/nmz→4[Fe23+]O3(magnetite)+Fe2++2/nmz−n and 3 [ Fe 2 + Ti ] O 3 (ilmenite) + 2 / n m z &#x2192; Fe 2 3 + Ti 3 O 9 (pseudorutile) + Fe 2 + + 2 / n m z &#x2212; n , "> 3[Fe2+Ti]O3(ilmenite)+2/nmz→Fe23+Ti3O9(pseudorutile)+Fe2++2/nmz−n, where z is the valance state and n is the charge transfer number. The half cell potential range for solid state oxidation [Fe(II)] → [Fe(III)] is −0.34 to −0.65 V, making structural Fe(II) a stronger reducing agent than aqueous Fe 2+ (−0.77 V). Reduction rates for aqueous metal species are linear with time (up to 36 h), decrease with pH, and have rate constants between 0.1 and 3.3 × 10 −10 mol m −2 s −1 . Iron is released to solution both from the above reactions and from dissolution of the oxide surface. In the presence of chromate, Fe 2+ is oxidized homogeneously in solution to Fe 3+ . X-ray photoelectron spectroscopy (XPS) denotes a Fe(III) oxide surface containing reduced Cr(III) and V(IV) species. Magnetite and ilmenite electrode potentials are insensitive to increases in divalent transition metals including Zn(II), Co(II), Mn(II), and Ni(II) and reduced V(IV) and Cr(III) but exhibit a log-linear concentration-potential response to Fe(III) and Cu(II). Complex positive electrode responses occur with increasing Cr(VI) and V(V) concentrations. Potential dynamic scans indicate that the high oxidation potential of dichromate is capable of suppressing the cathodic reductive dissolution of magnetite. Oxide electrode potentials are determined by the Fe(II)/Fe(III) composition of the oxide surface and respond to aqueous ion potentials which accelerate this oxidation process. Natural magnetite sands weathered under anoxic conditions are electrochemically reactive as demonstrated by rapid chromate reduction and the release of aqueous Fe(III) to experimental solution. In contrast, magnetite weathered under oxidizing vadose conditions show minimum reactivity toward chromate ions. The ability of Fe(II) oxides to reduce transition metals in soils and groundwaters will be strongly dependent on the redox environment.

Geochimica et Cosmochimica Acta↗

Rapid serological analysis of bacterial lipopolysaccharides by electrotransfer to nitrocellulose

Techniques are described for the rapid screening of proteinase K-treated bacterial lysates by electroblot and immunoenzymatic detection to assess O-specificity of antigens and antisera. Conditions are outlined which permit the use of a single polyacrylamide gel for both electrotransfer to nitrocellulose and silver staining. Immunodetection of transferred LPS bands was equally sensitive to silver stain when whole cell or O-specific antisera were used. The techniques were utilized to identify at least 4 O-serotypes among sorbitol fermenting isolates of the fish pathogen, Yersinia ruckeri . Observed variations in the electrophoretic mobilities of lipopolysaccharides from 17 field isolates of Y. ruckeri were used to accurately predict the O-serotype.

Journal of Immunological Methods↗

A herringbone bedform pattern of possible Taylor-Görtler type flow origin seen in sonographs

Side-scan sonar records collected in a shallow arctic lagoon (2&ndash;2.5 m depth) reveal a herringbone pattern of current-aligned linear reflectors with branching diagonals. The major longitudinal reflectors have no detectable relief (<20 cm), are spaced 5&ndash;10 m apart, and may represent current-aligned helical cell boundaries preserved in the silty fine sand of the lagoon floor. The pattern suggests a three-dimensional flow regime of the Taylor-G&ouml;rtler type.

Sedimentary Geology↗

A proposed mechanism for the formation of spherical vivianite crystal aggregates in sediments

Vivianite [Fe 3 (PO 4 ) 2 ·8H 2 O] is often found in the form of nodules composed of spherical aggregates of crystals. Crystallization of vivianite in agar gels of various concentrations yield crystal aggregates (nodules) that have spherical morphology and a bimodal size distribution. The aggregates were formed under both biotic and abiotic conditions. When special redox cells fitted with electrodes were used, more perfect spherical structures were formed when the electrodes were shorted than when they were on open circuit. In nature, vivianite nodules generally are found in sediments or clays that are gelatinous, often caused by the presence of organic debris. A model consistent with experimental observations and based on the dynamics of gels is proposed to explain a possible origin of nodular vivianite. To maintain iron and phosphate concentrations in sedimentary pore spaces filled with gel-like organic debris, the electric field spanning the aerobic-anerobic zones in the upper sediments may be an important driving force in addition to diffusion. It is suggested that the combination of the gel medium in the pore spaces and the natural electric field in the upper sediments could be contributing causes to explain the spherical aggregates of vivianite crystals found in nature.

Sedimentary Geology↗

An ion-selective electrode method for determination of chlorine in geological materials

A method is presented for the determination of chlorine in geological materials, in which a chloride-selective ion electrode is used after decomposition of the sample with hydrofluoric acid and separation of chlorine in a gas-diffusion cell. Data are presented for 30 geological standard materials. The relative standard deviation of the method is estimated to be better than 8% for amounts of chloride of 10 μg and greater.

Talanta↗

Embryotoxic and biochemical effects of waste crankcase oil on birds' eggs

Waste crankcase oil (WCO) is a major source of oil pollution in both the aquatic and terrestrial environment and has been implicated in the poisoning of mammals and fish. It is also mutagenic. Since birds' eggs are highly sensitive to external microliter applications of environmentally polluting oils, we examined the developmental effects of external applications of WCO on eggs of the mallard duck (Anas platyrhynchos) and the bobwhite quail (Colinus virginianus). At 48 hr of development, mallard eggs were exposed externally to 2, 5, or 15 :l of WCO or 15 :l of clean crankcase oil (CCO) while bobwhite eggs received proportional doses of 0.5, 1, or 3 :l of WCO and 3 :l of CCO in a similar manner. WCO was highly embryotoxic to both species compared to CCO and resulted in dose-dependent mortality, reduced growth, and abnormal survivors. Application of 15 :l WCO resulted in 84% mortality in mallards and 3 :l WCO resulted in 88% mortality in bobwhites. Abnormal survivors included embryos with subcutaneous edema, incomplete ossification, and eye and brain defects. Red blood cell *-aminolevulinic acid dehydratase (ALAD) activity, liver ALAD activity, and hemoglobin concentration were significantly lower after treatment with WCO in embryos and hatchlings of both species. Plasma uric acid, plasma alanine aminotransferase (ALT), and plasma aspartate aminotransferese (AST) were significantly elevated in WCO-treated mallards after hatching. Biochemical effects, growth retardation, and mortality at proportionally lower dose levels were more pronounced in mallards than in bobwhites. Chemical analysis of the WCO and CCO revealed a considerably higher content of aromatic hydrocarbons in WCO than in CCO. Lead levels were highly elevated in WCO (4600 ppm) compared to CCO (2 ppm).

Toxicology and Applied Pharmacology↗

Immune response of channel catfish, Ictalurus punctatus Rafinesque, to bacterial and protozoan antigens administered by three routes

Experiments were conducted to measure the agglutinating antibody response of channel catfish to a particulate and a soluble antigen administered simultaneously by one of three routes. Specific antibody production in response to administration of particulate brucella tube-test antigen via intramuscular injection, oral drench, and topical application peaked at 3 weeks in channel catfish held under identical conditions at 21°C. The humoral antibody response was greater in fish injected with antigen than in the orally or topically exposed channel catfish. Specific antibody was also produced by the same channel catfish in response to the administration of a soluble ciliary preparation derived from Tetrahymena pyriformis Lwoff. Intramuscular injection of Tetrahymena antigen was the only route that produced detectable levels of circulating antibody as measured by direct agglutination of live T. pyriformis cells. The response to the soluble antigen also peaked at 3 weeks. Neither antigen elicited detectable agglutinins in cutaneous mucus, regardless of the vaccination method used.

Aquaculture↗

Nutritional value of dietary nucleic acids and purine bases to rainbow trout (Oncorhynchus mykiss)

Rainbow trout were fed diets with graded levels (0.6%, 1.6%, 2.5%, and 4.1%) of a yeast nucleic acid extract corresponding to dietary Saccharomyces cerevisiae levels of 7.5%, 20%, 30% and 50% or diets supplemented isonitrogenously (0.8% N) with free purines (adenine, guanine, xanthine, and hypoxanthine) in two 12-week studies. Fish fed increasing levels of yeast extract manifested significant ( P < 0.05) corresponding incremental increases in growth and nitrogen retention. No negative effects on feed intake were observed. When fish were fed supplemental free purines, adenine was shown to be a potent inhibitor of feed intake and growth. While supplementation with the remaining purines did not negatively affect feed intake or growth, carcass nitrogen retention was significantly depressed, indicating the lack of a nitrogen-sparing effect. Our results indicate that the nutritional significance of free dietary adenine versus nucleic acid-bound adenine in yeast or yeast nucleic acid is an important consideration in evaluating the suitability of single cell proteins in fish feed formulations.

Aquaculture↗

Application of a simple cerebellar model to geologic surface mapping

Neurophysiological research into the structure and function of the cerebellum has inspired computational models that simulate information processing associated with coordination and motor movement. The cerebellar model arithmetic computer (CMAC) has a design structure which makes it readily applicable as an automated mapping device that "senses" a surface, based on a sample of discrete observations of surface elevation. The model operates as an iterative learning process, where cell weights are continuously modified by feedback to improve surface representation. The storage requirements are substantially less than those of a conventional memory allocation, and the model is extended easily to mapping in multidimensional space, where the memory savings are even greater. ?? 1991.

Computers & Geosciences↗

Metal contamination in wildlife living near two zinc smelters

Wildlife in an oak forest on Blue Mountain was studied 10 km upwind (Bake Oven Knob site) and 2 km downwind (Palmerton site) of two zinc smelters in eastern Pennsylvania, USA. Previous studies at sites near these smelters had shown changes in populations of soil microflora, lichens, green plants and litter-inhabiting arthropods. The 02 soil litter horizon at Palmerton was heavily contaminated with Pb (2700 mg kg −1 ), Zn (24 000 mg kg −1 ), and Cd (710 mg kg −1 ), and to a lesser extent with Cu (440 mg kg −1 ). Various kinds of invertebrates (earthworms, slugs and millipedes) that feed on soil litter or soil organic matter were rare at, or absent from, the Palmerton site. Those collected at Bake Oven Knob tended to have much higher concentrations of metals than did other invertebrates. Frogs, toads and salamanders were very rare at, or absent from, the Palmerton site, but were present at Bake Oven Knob and at other sites on Blue Mountain farther from the smelters. Metal concentrations (dry wt) in different organisms from Palmerton were compared. Concentrations of Pb were highest in shrews (110 mg kg −1 ), followed by songbirds (56 mg kg −1 ), leaves (21 mg kg −1 ), mice (17 mg kg −1 ), carrion insects (14 mg kg −1 ), berries (4·0 mg kg −1 ), moths (4·3 mg kg −1 ) and fungi (3·7 mg kg −1 ). Concentrations of Cd, in contrast, were highest in carrion insects (25 mg kg −1 ), followed by fungi (9·8 mg kg −1 ), leaves (8·1 mg kg −1 ), shrews (7·3 mg kg −1 ), moths (4·9 mg kg −1 ), mice (2·6 mg kg −1 ), songbirds (2·5 mg kg −1 ) and berries (1·2 mg kg −1 ). Concentrations of Zn and Cu tended to be highest in the same organisms that had the highest concentrations of Cd. Only a small proportion of the metals in the soil became incorporated into plant foliage, and much of the metal contamination detected in the biota probably came from aerial deposition. The mice from both sites seemed to be healthy. Shrews had higher concentrations of metals than did mice, and one shrew showed evidence of Pb poisoning; its red blood cell ALAD activity was greatly reduced, one kidney contained acid-fast intranuclear inclusion bodies, and the other kidney had 280 mg kg −1 Pb (wet wt). The livers from two cuckoos from Palmerton had elevated Pb concentrations (18 and 25 mg kg −1 , wet wt). Most of the songbirds seemed to be healthy.

Pennsylvania↗

Lead concentrations and reproductive success in European starlings Sturnus vulgaris nesting within highway roadside verges

In 1981, the authors studied lead concentrations and reproductive success in free-living European starlings Sturnus vulgaris nesting within the verges of two Maryland highways with different traffic volumes, Route 197(average daily traffic volume[ADT] = 10,800 vehicles) and the Baltimore-Washington Parkway (ADT=52,500 vehicles) and a nearby control area. Concentrations (mg kg-1 dry weight) of lead in the ingesta (84-94 mg kg-1), carcasses (4.0-9.6 mg kg-1)and feathers (6.8-52 mg kg-1) of Parkway nestlings and adults were 3 to 13 times those found in starlings from the control area, whereas lead concentrations in the ingesta and tissues of starlings from the verge of Route 197 were similar to those of controls. Activity of delta-aminolevulinic acid dehydratase (ALAD) in red blood cells (RBCs) of adult and nestling starlings from the Parkway was depressed from 43 to 60% compared to controls. RBC ALAD activity in adults from nests along Route 197 was similar to that of adult starlings from the control area, but that of their young was depressed 17%. Haemoglobin concentrations (-16%) and haematocrits (-10%) in Parkway nestlings were depressed compared with those of nestlings from the other two study areas, whereas those of adults were not affected. Clutch size, number of young hatched and the number of young in nests 1 to 3 days before fledging were similar among sites, as were body weights of adults and prefledging weights of their young. However, brain weights of Parkway nestlings were lower (P < 0.05) than those of nestlings from the other study areas. Results suggests that lead within verges of major highways probably does not pose a serious hazard to adult ground-foraging songbirds. However, the effects of lead-induced reductions in haemoglobin concentration, haematocrit, RBC ALAD activity and brain weight on the postfledging survival of their young are not known.

Environmental Pollution (Series A)↗