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1.
Mean daily consumption rates on Mytilus spp. were compared among juveniles of the non-indigenous Carcinus maenas, juveniles of the indigenous Cancer irroratus, and adults of the indigenous Dyspanopeus sayi between June and August 2005 to assess the relative impact of juvenile C. maenas in field (Benacadie Channel (45°54′ N, 60°53′ E), Bras d’Or Lakes, Nova Scotia, Canada) and laboratory experiments. This study examined: (1) whether consumption rates in a field setting vary among species; (2) the effect of laboratory and field settings on species-specific consumption rates, and whether rates vary between settings for each species; and (3) the effects of temperature and salinity on the consumption rates of these species. In field experiments, there was no significant difference in consumption among C. maenas, C. irroratus, and D. sayi (0.100?±?0.067, 0.450?±?0.189, and 0.800?±?0.423 mussels crab?1 d?1, respectively). However, both C. maenas and C. irroratus consumed two to four times more prey in the laboratory than in the field. D. sayi prey consumption was also greater (although not significant) in the laboratory than in the field. In the laboratory, consumption rate was greater for C. irroratus in salinities of 26 than 17 (2.75 and 1.69–1.81 mussels crab?1 d?1, respectively), and in 17°C than 13°C (1.10–1.21 and 0.56–0.64 mussels crab?1 d?1, respectively) for C. maenas. In all experiments, consumption rates of juvenile C. maenas were lower than or similar to those of the juvenile and adult indigenous species, suggesting that the potential predatory impact of juvenile C. maenas on Mytilus spp. may not be as significant as that of the adults of this non-indigenous species.  相似文献   

2.
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.  相似文献   

3.
The combination of cathodoluminescence (CL) analysis, temperature and temperature–time calculations, and microstructural numerical modelling offers the possibility to derive the time-resolved evolution of a metamorphic rock. This combination of techniques is applied to a natural laboratory, namely the Ballachulish contact aureole, Scotland. Analysis of the Appin Quartzite reveals that the aureole was produced by two distinct magmatic events and infiltrated by associated fluids. Developing microstructures allow us to divide the aureole into three distinct regions. Region A (0–400?m, 663°C?<?T max?<?714°C) exhibits a three-stage grain boundary migration (GBM) evolution associated with heating, fluid I and fluid II. GBM in region B (400–700?m, 630°C?<?T max?<?663°C) is associated with fluid II only. Region C (>700?m of contact, T max?<?630°C) is characterised by healed intragranular cracks. The combination of CL signature analysis and numerical modelling enables us to recognise whether grain size increase occurred mainly by surface energy-driven grain growth (GG) or strain-induced grain boundary migration (SIGBM). GG and SIGBM result in either straight bands strongly associated with present-day boundaries or highly curved irregular bands that often fill entire grains, respectively. At a temperature of ~620°C, evidence for GBM is observed in the initially dry, largely undeformed quartzite samples. At this temperature, evidence for GG is sparse, whereas at ~663°C, CL signatures typical for GG are commonplace. The grain boundary network approached energy equilibrium in samples that were at least 5?ka above 620°C.  相似文献   

4.
The estuarine opossum shrimp Mysidopsis almyra Bowman is a useful laboratory organism and has been cultured continuously for over three years in a recirculating artificial seawater system. This system is composed of one 57 1 and one 19 1 glass aquarium joined by a power filter and siphons. Optimal culture conditions are 20 ppt artificial seawater at 25°C and a 14∶10 hour light∶dark photoperiod. Adult mysids are maintained in the large aquarium and fed newly hatched nauplii of Artemia salina. Newly hatched M. almyra postlarvae are carried by the siphons into the smaller aquarium where they are trapped in cylinders made of 0.3 mm nesh nylon netting. One-hundred to four-hundred post-larvae are harvested each day from the system.  相似文献   

5.
A laboratory heating experiment was conducted in an attempt to evaluate the possible role of lipids as precursors for petroleum hydrocarbons. Lipids were extracted from a Recent lake sediment (Lake Haruna, Japan), and heated under N2 atmosphere, at 125–370°C, for 1–7 days. A significant amount of lipids was polymerized to kerogen-like matter (lipid-derived kerogen) at the low temperature of 175°C for 1 day. The polymerization follows first-order kinetics, and the half life of lipids is calculated to be 104–105 yr at 0–30°C. The lipid-derived kerogen generated a significant amount (62 mg/g) of n-alkanes (C14–C36) on heating at 350°C for 1 day.The results indicate a possible occurrence of lower temperature thermal polymerization of lipids in a relatively early stage of diagenesis as one of the formation pathways of kerogen with high hydrocarbon producing potential.  相似文献   

6.
Constant-temperature laboratory culture experiments of the planktonic foraminiferal species Globigerinoides sacculifer (Brady) suggest that the ratios of Li and Sr to Ca in the shells are a function of these ratios in the culture solutions. MgCa and NaCa in the shells did not vary with changes of these ratios in the culture solution. These are the first direct determinations of the relationship between foraminiferal shell chemistry and solution composition.The possibility of temperature dependence for the minor elemental composition of foraminiferal shells was also investigated in the laboratory and by analysis of several planktonic and one benthic foraminiferal species from sediment trap and sediment core samples. The SrCa, MgCa, and NaCa ratios in the natural samples roughly correlate with calcification temperature, whereas differences in the Li/Ca ratios are small and not systematically related to temperature. However, laboratory culture experiments at 20°C and 30°C showed no variation in the LiCa, SrCa, MgCa, and NaCa ratios with calcification temperature for the planktonic foraminifera G. sacculifer and Orbulina universa. Therefore, observed differences in the SrCa, MgCa, and NaCa ratios for the sediment trap and core foraminiferal samples cannot be ascribed to direct effects of calcification temperature, but may be due to some other environmental factor which is correlated with temperature.  相似文献   

7.
An integrated structural, petrographic and microthermometric methodology has been applied on syn- to late-orogenic quartz veins from the High-Ardenne slate belt (Belgium) to define their relative timing. The quartz precipitates, which do not show any mutual cross-cutting relationships, represent the meso-scale brittle accommodation during fold initiation, amplification and locking. Crystal-plastic deformation structures and P–T trapping conditions indicate that the different processes accommodating folding occurred in a progressive manner along a retrograde deformation path, associated with the gradual exhumation of the slate belt from ca. 7.5 to 6 km depth. Successive veining occurred from peak metamorphic conditions (ca. 300 °C and 190 MPa), measured in extrados veins, to subsequent lower P–T conditions in the periphery of a lenticular vein (ca. 275 °C and 180 MPa), late-orogenic saddle reef filling (ca. 245 °C and 160 MPa), and the core of a lenticular vein (ca. 220 °C and 150 MPa). Open-cavity growth and fluid-assisted brecciation indicate that veining occurred under overpressured fluid conditions. It is therefore fair to assume that the High-Ardenne slate belt acted – at least episodically – as a mid-crustal overpressured fluid reservoir, not only in the earliest and latest stages, but also during the main stage of orogeny.  相似文献   

8.
Amelia albite annealed at > 1080 °C for 3200 hrs by Duba and Piwinskii (1974) shows very fine twin lamellae (～1 μm) after the albite law, suggesting that it once underwent transformation into monalbite. A fragment of this specimen was investigated at 27 °C, 300 °C, 550 °C, 800 °C and 930 °C using the high-temperature precession technique. As the temperature increases, the splitting angle of c *-axes (likewise c *-axes) of two twin individuals continues to decrease. The photographs taken at 930 °C show that these two splitting angles have converged to 0o, indicating completion of the transformation into monalbite. The transition point we observe supports the results of MacKenzie (1952) (920±20 °C) and Grundy et al. (1967) (930 °C) rather than those of Sueno et al. (1973) and Prewitt et al. (1974) (> 1080 °C); the discrepancy is most likely due to the differences in the degree of Al-Si disorder of the samples used in the experiments.  相似文献   

9.
The paper presents critical analysis of literature data on the stability constants of aqueous species in the system Zn-O-H-S?II-Cl. In order to more accurately determine the composition and stability of chloride Zn complexes, additional experiments were carried out to determine the solubility of sphalerite ZnSc in chloride-sulfide solutions at 175°C and the saturated vapor pressure of the solution. Having processed the data, we obtained the thermodynamic properties at 25°C and parameters of the HKF (Helgeson-Kirkham-Flowers) equation of state (EoS) for hydroxide, chloride and hydrosulfide Zn complexes. The constants of sphalerite dissolution reactions with the formation of hydrosulfide and, particularly, chloride complexes increase with increasing temperature. The predominant Zn transport species in high-temperatures (>250°C) chloride-sulfide hydrothermal solutions are chloride complexes, first of all, ZnCl 4 2? . As the temperature decreases, the concentrations of complexes with smaller numbers of Cl? ligands increase. The region of weakly acidic to alkaline pH is dominated by hydrosulfide Zn complexes, but their concentrations in equilibrium with sphalerite are relatively low (a few ppm at 400°C and S concentrations <0.1 mol kg?1) and decreases with a temperature decrease. In the region dominated by chloride complexes, the concentration of dissolved Zn can amount to a few fractions of a percent at near-neutral pH, 400°C, and m(NaCl) = 1.0 and increases if the fluid becomes more acidic. An extremely important factor controlling the concentrations of dissolved Zn is temperature: cooling leads to the effective precipitation of sphalerite, particularly in the region dominated by chloride complexes. The thermodynamic properties of the solid phases and parameters of the HKF model for aqueous species in the system Zn-O-H-S-II-Cl are presented in the on-line version of the FreeGC database (http://www-b.ga.gov.au/minerals/research/methodology/geofluids/thermo/calculator/search.jsp), which enables calculating the Gibbs energy values of components of the system and reaction constants involving these components at PT parameters up to 600°C and 3 kbar.  相似文献   

10.
The electrical conductivity of calcite cleavage fragments was measured using direct current. Five temperature intervals, characterized by different activation energies of conduction, were established — T 1: (300°)–500° C, T 2: 500–725° C, T 3: 725°–800° C, T 4: 800°–985° C and T 5: 985°–(1,200)° C. The data above 600° C indicate various intrinsic conduction mechanisms which are likely to be related to disorder in the CO3-sublattice of calcite. The transitions between the temperature intervals T 2-T 3-T 4 and T 4-T 5 are probably correlated with high-temperature transitions of calcite at 800° and 985° C. Measurement of the thermoelectric voltage indicates a conductivity dominated by negatively charged carriers.  相似文献   

11.
MX-1 tridymite is one of the room-temperature polymorphs of SiO2 tridymite and has an underlying monoclinic structure (Cc) with incommensurate modulations along a * and c * (Hoffmann et al. 1983; Löns and Hoffmann 1987). With increasing temperature up to 500° C, MX-1 is reported to experience at least five structural phase transitions. However, its structures and the relationships to other tridymite polymorphs are unclear. We present here a 29Si MAS NMR study of the room-temperature incommensurate structure of MX-1 and its structural phase transitions up to 540° C. Our results suggest that at room temperature, all the Si sites in MX-1 tridymite are in positions with similiar ∠Si-O-Si of ～150° and are consistent with the presence of two incommensurate modulations proposed by Hoffmann et al. (1983). Simulations of the spectra yield modulation amplitudes of 1.33 and 0.87 ppm, corresponding to 0.009 and 0.006 Å for Si-Si. The maximum atomic displacements along a and b due to the modulations appear to be ～0.01–0.02 Å. The structural phase transitions of MX-1 are significantly different from those of MC tridymite below 220° C. Our high temperature results confirm that MX-1 tridymite transforms to the H5 phase at about 65° C. The most important transition occurs near 110° C, where the H5 phase transforms to a phase yielding a single, narrow NMR peak, indicating the disappearance of the superstructure and possibly the onset of the dynamic averaging. The NMR lineshapes of H5 are consistent with the metrically orthorhombic unit cell and commensurate superstructure of 2a, 2b and 10c proposed by Graetsch and Flörke (1991). The phase present above 110° C is probably similar to the OC phase, but has a mean ∠Si-O-Si of ～152.0° at 113° C, 152.9° at 185° C and 154.1° at 500° C. The transitions at ～160 and 220° C for MX-1 are subtle and probably due to impurity MC. Analysis of the modulations in the OS phase of MC tridymite indicates that their amplitudes are of the order of 0.02 Å, significantly less than the value 0.3 Å proposed by Nukui et al. (1979).  相似文献   

12.
It is attempted to determineT, P values for the lowgrade metamorphic facies. From geologic-petrographic observations and from experiments mineralreactions are outlined which characterize the zeolitic-, the glaucophane- and the greenschistfacies, respectively. Only such reactions are considered which are univariant if Pf=Ps; thus aP-T grid can be arrived at. Experimental data on the equilibria of the relevant reactions is taken from the literature and from own experiments. Experimental results are always checked against known field-observations. Contrary to current opinium, we arrive at rather higher temperatures for the beginning of the lowgrade metamorphic facies: Diagenesis. From sedimentation up to slightly below 300° C. Zeolitic facies. From slightly below 300° C up to about 400° C. Greenschistfacies. From about 400° C up to about 550° C. Glaucophaneschistfacies. Under pressures of at least 6–7 kb this facies begins somewhat above 300° C, probably at about 330° C, grading into high-pressure greenschistfacies.  相似文献   

13.
Four distinct components of natural remanent magnetization were isolated from a single site in welded tuffs in the Upper Cretaceous Kisin Group of the Sikhote Alin mountain range, Russia. In order to contribute toward a basis for an interpretation of multicomponent magnetization, rock magnetic experiments were performed on the welded tuffs. All four magnetization components essentially reside in magnetite. The lowest-temperature component up to 300 °C (component A: D=349.3°, I=60.9°, α95=7.3°, N=7) is a present day viscous magnetization. The third-removed component (component C: D=41.4°, I=51.8°, α95=3.5°, N=8), isolated over the temperature range of 450–560 °C, is a primary remanence. The second- and fourth-demagnetized components (component B: D=174.7°, I=−53.1°, α95=21.2°, N=3 and component D: D=188.1°, I=−64.5°, α95=4.0°, N=8, respectively) are secondary magnetizations related to a thermal event in Sikhote Alin between 66 and 51 Ma. Components B and D were acquired through different remagnetization processes. Component B is ascribed to a thermoviscous remanent magnetization carried by single-domain magnetite, and component D is a chemical remanent magnetization.  相似文献   

14.
The influences of temperature and environmental hypoxia on the growth rates of two California anadromous fishes, white sturgeon (Acipenser transmontanus) and striped bass (Morone saxatilis) were examined. Fish (0.5–0.6 g initial weight) were fedad libitum rations ofArtemia in flow-through aquaria regulated for temperature (15, 20, and 25°C) and oxygen tension (130 and 90 torr Po 2). Growth of sturgeon was significantly greater at 20 °C compared with 15 °C, but there was no difference between 20 and 25 °C. Striped bass growth increased with each 5° increment of temeprature elevation to 3.2% body weight per d at 25 °C, the fastest growth rate measured. The temperature of maximum growth reflected the temperature of the native estuarine rearing area. Environmental hypoxia (90 torr Po 2) reduced growth of sturgeon within each temperature level, whereas striped bass growth was reduced by hypoxia only at the upper two temperatures. Sturgeon were much more active in the growth chambers than striped bass. Sturgeon activity increased with each 5 °C temperature increase under normoxia and hypoxia, except at 25 °C (hypoxia) where activity was insignificantly different from that at 20 °C (hypoxia).  相似文献   

15.
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.  相似文献   

16.
The thermal expansion of anhydrite, CaSO4, has been measured from 22° to 1,000° C by X-ray diffraction, using the Guinier-Lenné heating powder camera. The heating patterns were calibrated with Guinier-Hägg patterns at 25° C, using quartz as internal standard. Heating experiments were run on natural anhydrite (Bancroft, Ontario), which at room temperature has lattice constants in close agreement with those of synthetic material. The orthorhombic unit cell at 22° C (space group Amma) has a=7.003 (1) Å, b=6.996 (2) Å and c=6.242 (1) Å, V=305.9 (2) Å3. At room temperature, the thermal expansion coefficients α and β (α in °C?1×104, β in °C?2×108) are for a, 0.10, ?0.69; for b, 0.08, 0.19; for c, 0.18, 1.60; for V, 0.37, 1.14. Second-order coefficients provide an excellent fit over the whole range to 1,000° C.  相似文献   

17.
Melt inclusions in olivine and pyroxene phenocrysts in kersantite and camptonite at Chhaktalao in Madhya Pradesh, India are mainly of the evolved type forming daughter minerals of olivine, pyroxene, plagioclase, spinel, mica, titanomagnetite and sulphides. Heating studies exhibit a temperature range from 1215° to 1245°C for the melt inclusions in olivine in camptonite and 1220–1245°C for olivine in kersantite. The temperature for melt inclusions in pyroxene ranged from 1000° to 1150°C in camptonite and 850–1100°C for pyroxene in kersantite. The bubble inside these melt inclusions is mainly CO2. The Th°C of CO2 into liquid phase occurred between 26° and 31°C in olivine and 25–30°C in pyroxene from kersantite and camptonite. The maximum density estimated is 0.72 g/cm3 and the minimum is 0.45 g/cm3. The depth of entrapment of the melt inclusion is estimated between 10–15 km. The pressure of entrapment of melt inclusion in olvine is 4.6 kbar where as that in pyroxene is 3.7 kbar. The lamprophyres in the Chhaktalao area are considered to be derived from low depth and low pressure region, possibly within spinel lherzolite zone.  相似文献   

18.
Zhang and Sachs [Hydrogen isotope fractionation in freshwater algae: I. Variations among lipids and species. Organic Geochemistry 38, 582–608, 2007] demonstrated that algal lipid δD values track water δD values with high fidelity (R2 > 0.99), but that D/H fractionation varied among lipids and algal species. Here we report on the influence of temperature and nitrogen limitation on D/H fractionation in lipids from cultured microalgae. Two species of freshwater green algae, Eudorina unicocca and Volvox aureus, were grown in batch culture at 15 °C and 25 °C. Increased D/H fractionation of 2?4‰/°C occurred at the higher temperature in all lipids analyzed. The marine diatom Thalassiosira pseudonana was grown in continuous culture under nitrogen replete (NR) and nitrogen limited (NL) conditions, resulting in a growth rate that was 4.4 fold lower under the latter conditions. The fatty acid content of NL cells was approximately 4 fold higher than in NR cells, whereas the sterol content was similar in both. While sterols from the NL culture were enriched in deuterium by 37‰ relative to the NR culture, fatty acids from both cultures had similar δD values, implying that D/H fractionation during isoprenoid (branched) lipid synthesis is affected by nitrogen limitation, but D/H fractionation during acetogenic (linear) lipid synthesis is not. Cross-talk of the precursor isopentenyl diphosphate between the cytosolic MVA and plastidic DOXP/MEP synthetic pathways is a plausible mechanism for the observed D/H differences between isoprenoid and acetogenic lipids. This preliminary study highlights the need to consider both the type of lipid and potential changes in growth conditions in paleoenvironmental studies using lipid D/H ratios.  相似文献   

19.
Heat of solution measurements in an oxide-melt were performed on samples of natural sillimanite heat-treated in the range 1200–1700°C at pressures of 16–23 kbar. A distinct enthalpy of solution decrement relative to the unheated sillimanite of about 1.3 kc/mole is shown by samples run at 1400–1550°C. Pressure variations in the range 16–23 kbar cause little change in the heat of solution in this temperature range. This pressure-independent ‘plateau’ in heat of solution is interpreted to be due to Al-Si disordering on tetrahedral sites in the sillimanite structure. A simple temperature-dependent disordering model developed by navrotsky and Kleppa (1967) for spinels leads to an Al-Si interchange enthalpy, ΔHnt, of16 ± 1 kcal/mole, in good agreement with the value derived by Holdaway(1971) on entirely different grounds.Above 1550°C, larger heat of solution decrements were observed. Microprobe analyses of quenched samples indicate that the sillimanite has not deviated significantly from the ideal formula. Some unknown profound disordering process may account for the heat effects in the very high temperature range.Unit cell volumes of quenched samples also describe a ‘plateau’ region in the temperature range 1400–1550°C. This plateau consists of an increase of the 6 crystallographic axis beginning at 1350°C without much change in the other axes in the range 1350–1550°C. A sudden expansion of the α-axis occurs between 1550 and 1630°C.We conclude that Al-Si disorder of the type postulated by Beger et al. (1970), and Holdaway (1971) has been confirmed calorimetrically for samples heated under pressure in the temperature range 1400–1550°C.  相似文献   

20.
The distribution of interatomic distances in amorphous NaAlSi3O8 has been determined at 805°C by X-ray radial distribution analysis to investigate structural differences between the glass (T < 763°C) and the supercooled liquid (763°C < T < 1118°C). Except for slight differences attributable to thermal expansion, no significant changes were observed. The sample crystallized during the course of the experiment, but at least one crystal-free data set was obtained. The transition from the inferred six-membered ring structure of the supercooled liquid to the four-membered ring structure of the crystal was clearly visible in radial distribution function (RDF's) determined before and after crystallization.RDF's were also determined at 25°C for two NaAlSi3O8 glasses with different histories. The first was derived from a melt that had been cooled slowly from 1600 to 32°C above the melting point (Tf = 1118°C) to detect possible repolymerization to a more ‘crystal-like’ structure as the melt approached Tf. The second glass was prepared by holding a single crystal of Amelia albite at 50°C above Tf to see if the crystalline four-membered ring structure was preserved in melts at temperatures just above the liquidus. No significant differences were observed between these two RDF's and one obtained from a glass quenched from 1800°C. These results suggest that in addition to the destruction of formation of a periodic structure, melting and crystallization in NaAlSi3O8 also involves a repolymerization of tetrahedra. This would explain the observed kinetic barrier to melting and crystallization in the anhydrous system and the catalytic effect of small amounts of water or alkali oxide.  相似文献   

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