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1.
  1. As there was a paucity of information on the aquatic decomposition of leaves of willow (Salix alba), poplar (Populus gr. nigra) and alder (Alnus glutinosa), the net-bag technique was used to study chemical changes in the leaves over a period of six months in the Garonne (France).
  2. The disappearance rates of foliar organic matter were about similar for the three species (k = 0.0065 day?1 for alder, k = 0.0054 day?1 for poplar and k = 0.0050 day?1 for willow). Changes in carbon amount were comparable to those of organic matter. Nitrogen and organic phosphorus accumulated during the first months of decomposition. The C/N ratios of foliar matter changed in the same way in the three species, falling steeply for the first month, then levelling off. Amounts of sugar disappeared very rapidly, particularly for alder and willow. Cellulose concentrations were constant throughout the whole decomposition process whilst an increase in the amounts of lignin was observed during the first months; however the latter could be due to an interference by microbial compounds.
  3. The changes of some constituents, such as carbon, sugars and cellulose, were described with exponential or multiexponential models. Despite the very different initial ratios of C/N and lignin/N, these changes associated with leaf decomposition were similar for the three species.
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2.
The distributions of carbon, nitrogen and phosphorus in a moss community-soil system developed on a naked region in Rundvågskollane (69050'S, 39009'E), East Antarctica, were investigated in order to analyze the flow of matter in an Antarctic terrestrial ecosystem.
  1. The moss community was formed from many moss blocks of different sizes and was composed ofBryum pseudotriquetrum (Hedw.) Gaertn., Meyer et Scherb.,Ceratodon purpureus (Hedw.) Brid. andGrimmia lawiana J. H. Willis. The surface of the community was covered with cyanobacteria.
  2. It was estimated that nitrogen fixed by cyanobacteria flowed from these organisms to the moss and that little nitrogen was transported within the moss body.
  3. A large amount of phosphorus existed in the soil. The moss community had a high phosphorus content although the amount itself was relatively little due to the small phytomass.
  4. It seems that absorption of phosphorus from soil is difficult for moss, because of the paucity of water necessary for the movement of phosphorus and the suppressed growth of moss due to the arid conditions.
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3.
  1. During an investigation of the physiology of Azotobacter vinelandii with particular reference to polysaccharide formation, a suitable medium which was precipitate-free was developed by adding EDTA at a concentration of 50 mg/l to a basal medium containing one of eight different carbohydrates as sole carbon source.
  2. Acetylated alginate was always produced by the organism when cultured under defined conditions, regardless of the carbohydrate source incorporated in the basal medium.
  3. When EDTA was added to the medium, the bacteria produced acetylated polyuronides with a preponderance of mannuronic acid residues.
  4. A comparison of the infrared spectra of the alginate produced by Azotobacter vinelandii and the affect of EDTA upon the mannuronic acid/guluronic acid ratios of the alginate are reported.
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4.
  1. Growth of the floating aquatic weed, Salvinia, in sterile culture was exponential for at least 2 weeks under standardized conditions.
  2. Increase in light intensity or in CO2 resulted in increases in growth rate, but did not extend the exponential period of growth.
  3. This aquatic plant, like many others, discriminates against calcium relative to strontium.
  4. In culture Salvinia exhibited luxury consumption of N and P.
  5. Because of high C/N ratios, Salvinia may not be a favorable source of animal food, but might be useful in nutrient removal schemes.
  6. In sterile culture, S. molesta produced fewer leaves than S. minima, but maintained a significant increase in leaf area and dry weight. This may be correlated with the ability of the first species to rapidly spread over tropical waterways.
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5.
T. Kamaya 《Mycopathologia》1969,37(4):320-330
Young colonies of Sabouraud's glucose agar room temperature culture ofCandida species from human isolation were suspended in distilled water. The suspension was mixed with a solution of lysozyme and incubated in a 37° C water bath. Within 3–5 hours, various species ofCandida cells showed flocculation to varying degrees which occurred at varying periods of onset. Among sevenCandida species,Candida albicans andCandida stellatoidea showed the strongest flocculation, earliest onset and most solution clarity than did any other species.Candida stellatoidea was indistinguishable fromCandida albicans in its degree of flocculation, and in the clarity of solution.Candida species may be arranged in the following order according to their decreasing positivity in flocculation:
  1. Candida albicans
  2. Candida stellatoidea
  3. Candida tropicalis
  4. Candida krusei
  5. Candida pseudotropicalis
  6. Candida parapsilosis
  7. Candida guilliermondii
  8. Saccharomyces species may be placed afterCandida guilliermondii.
It seems possible to separate theCandida species into 3 groups by the rate of flocculation, and clarity of solution. Group I.Candida albicans andCandida stellatoidea. Group II.Candida tropicalis, C. krusei andCandida pseudotropicalis. Group III.Candida parapsilosis andCandida guilliermondii. Saccharomyces specimens (S. cerevisiae and others) were placed after group III.  相似文献   

6.
  1. The respiratory chain energy conservation systems of Bacillus megaterium strains D440 and M have been investigated following growth in batch and continuous culture. Respiratory membranes from these strains contained cytochromes b, aa 3 , o and b, c, a, o, respectively; both readily oxidised NADH but neither showed any pyridine nucleotide transhydrogenase activity.
  2. Whole cells of both strains exhibited endogenous →H-/O ratios of approximately 4; when loaded with specific substrates the resultant →H+/O ratios indicated that proton translocating loops 1 and 2 were present in strain D440 and that loops 2 and 3 were present in strain M.
  3. In situ respiratory activities were measured as a function of dilution rate during growth in continuous culture. True molar growth yields with respect to oxygen (Y O 2) of approximately 50 g cells·mole oxygen-1 were obtained for most of the nutrient limitations employed. Average values for Y ATP of 12.7 and 10.8 g cells·mole ATP equivalents-1 were subsequently calculated for strains D440 and M respectively.
  4. Energy requirements for maintenance purposes were low in energy-limited cultures but were substantially increased when growth was limited by nitrogen source (NH 4 + ). Under the latter conditions there is probably a partial uncoupling of energy-conserving and energy-utilising processes leading to energy wastage.
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7.
Improvements of the membrane filter method for DNA:rRNA hybridization   总被引:1,自引:1,他引:0  
We describe and recommend the following improvements of DNA:rRNA membrane filter hybridization methods. One of our aims was to avoid DNA release from filter discs during hybridization.
  1. Our hybridization conditions are 2 SSC in aq. dest., with 20% formamide, 50 C, overnight for 16 hr.
  2. Duplexing is over in 8–10 hr.
  3. Formamide has to be very pure (O.D.≤0.2/cm light path at 270 nm).
  4. RNAase treatment: 250 μg/5 ml 2 SSC/filter at 37 C for 1 hr.
  5. Our conditions for stepwise thermal denaturation are: 5°C steps from 50C to 90C in 1.5 SSC in 20% formamide.
  6. Single-stranded DNA, fixed on membrane filters, and stored in vacuo at 4C, can be used reliably for hybridization for up to 20 months.
  7. Concentrated DNA in 0.1 SSC, quick-frozen at ?50 C and stored at ?90 C for up to 2 years can be used for hybridization without much change.
  8. A CsCl gradient purification step yields much purer DNA, but increases the release of DNA from filters by about 20%. Filters with 20% more DNA is a compensation.
  9. rRNA can be stored for 20 months in SSC or 2 SSC at ?12C without changing the hybridization results.
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8.
  1. Out of 20 exogeneous substrates only ethanol and, to a much lesser extent, lactate and pyruvate were shown to be capable of stimulating the respiration of Acholeplasma laidlawii cells. However, none of these substrates changed the initial rate of active transport of 3-O-methyl-d-glucose (3-O-MG).
  2. From inhibitory analyses and spectroscopic data, it is apparent that the respiratory chain of A. laidlawii has no cytochromes and is probably not responsible for oxidative phosphorylation.
  3. Valinomycin and nigericin stimulated cell respiration only in the presence of K+-ions, while monensin stimulated it in the presence of Na+-ions.
  4. 3-O-MG transport was shown to be sensitive to uncouplers, ATPase inhibitors and arsenate are resistant to a majority of respiratory inhibitors tested. This suggested that there was no relationship between respiration and carbohydrate transport in the A. laidlawii cells. Further evidence was provided by the absence of respiratory stimulation during the transport of non-metabolizing carbohydrates.
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9.
The author investigated the presence of various carotenoids in the Echinodermata from Gullmar Fjord (Bohuslan, Sweden) by means of columnar and thin-layer chromatography. The investigations revealed the presence of the following:
  • - inHenricia sanguinolenta:β-carotene, echinenone, canthaxanthin, guraxanthin, lutein-5, 6-epoxide and astaxanthin.
  • - inAmphiura filiformis: canthaxanthin, cryptoxanthin, lutein, lutein-5, 6-epoxide, isozeaxanthin, zeaxanthin, astaxanthin and 4-hydroxy-4-keto-β-carotene.
  • - inAmphipholis squamata:β-carotene, cryptoxanthin, lutein, lutein-5, 6-epoxide, astaxanthin, astaxanthin ester, asterin-acid and rubixanthin derivative.
  • - inOphiopholis aculeata: canthaxanthin, cryptoxanthin, isozeaxanthin, astaxanthin, astaxanthin ester, asterinacid, 4-hydroxy-4-keto-β-carotene, hydroxy rubixanthin and gazaniaxanthin-like substances.
  • - inOphiothrix fragilis: canthaxanthin, lutein-5, 6-epoxide, isozeaxanthin, astaxanthin, astaxanthin ester, 4-hydroxy-4-keto-β-carotene, and hydroxy rubixanthin.
  • - inAntedon petatus:canthaxanthin, guaraxanthin, isozeaxan-thin, zeaxanthin, astaxanthin, astaxanthin ester and 4-keto-4-ethoxy-β-carotene.
  • - inEchinocardium cordatum:β-carotene,γ-carotene, canthaxanthin, lutein, isozeaxanthin, zeaxanthin, astaxanthin and astaxanthin ester.
  • - inSpatangus purpureus: isozeaxanthin, astaxanthin, astaxanthin ester and 4-hydroxy-4-keto-β-carotene.
  •   相似文献   

    10.
    The author investigated the carotenoids in the Echinodermata from Adriatic sea by means of columnar and thin-layer chromatography. The following carotenoids were identified:
  • - in Coscinasterias tenuispina: β-carotene, isocryptoxanthin lutein, lutein-5, 6-epoxide, 4-hydroxy-4-keto-β-carotene, zeaxanthin, astaxanthin and asterinacid.
  • - in Marthasterias glacialis: β-carotene, echinenone, cryptoxanthin, lutein, lutein 5, 6-epoxide, 4-hydroxy-4-keto-β-carotene, zeaxanthin, astaxanthin ester, astaxanthin and 3, 4-didehydro-α-carotene.
  • - in Paracentrotus lividus: β-carotene, echinenone, cryptothin, isocryptoxanthin, lutein, lutein-5, 6-epoxide, 4-hydroxy-4-keto-β-carotene, zeaxanthin, astaxanthin, astaxanthin ester and asterinacid.
  • - in Sphaerechinus granularis: ,β-carotene, echinenone, cryptoxanthin, lutein, lutein-5, 6-epoxide, astaxanthin and guaraxanthin.
  •   相似文献   

    11.
    Based on 388 parallel data of phytoplankton biomass and chlorophyll-a of two shallow lakes and two ponds, the following results were obtained:
    1. Relative chlorophyll-a content of phytoplankton biomass varied between 0.08–1.88%; chlorophyll-a concentration showed great differences among lakes.
    2. Significant correlations (r = 0.68–0.92) were established between phytoplankton biomass and chlorophyll-a concentration. The regression in the artificial ponds was non-linear.
    3. In parallel with the increase of average cell volume, a decrease in relative chlorophyll-a content was observed. A significant correlation (r = + 0.83) between the two variables was found. Relative chlorophyll-a content of phytoplankton is a log-function of average cell volume.
      相似文献   

    12.
    EPR spectroscopy is a powerful tool to identify at a molecular level, the different steps of catalyst preparation, and of catalytic reactions:
    1. Deposition of paramagnetic transition metal ions onto a support is monitored, and the coordination sphere of the metallic center is characterized by EPR.
    2. The catalyst is also characterized after activation (thermal oxidation or reduction):
  • - the distribution among the different sites in zeolites can be determined;
  • - the dispersion of the active phase may be appreciated;
  • - the unsaturation degree of the active site may be evaluated using probe molecules such as water or13C enriched carbon monoxide.
    1. The catalytic mechanisms can be investigated by studying the elementary steps of the catalytic reaction, as illustrated for methanol oxidation over Mo/SiO2 catalysts whose EPR results have extended the reaction mechanism proposed on the basis of kinetic data. In addition, reaction intermediates may be isolated inquasi-in situ conditions as in the case of olefin oligomerization catalyzed by Ni/SiO2 systems.
      相似文献   

    13.
    1. The lipid composition of mitochondria isolated from a fatty acid desaturase mutant ofSaccharomyces cerevisiae may be extensively manipulated by growing the organism on defined supplements of unsaturated fatty acid (UFA).
    2. The fatty acid composition of the mitochondrial lipids closely follows that of the whole cells from which the mitochondria are isolated. UFA-depleted mitochondria contain normal levels of sterols, neutral lipids and total phospholipids, but have much lower levels of phosphatidyl inositides.
    3. UFA-depleted mitochondria possess a full complement of cytochromes, oxidase both NAD-linked and flavoprotein-linked substrates at normal rates, and have levels of succinate and malate dehydrogenases similar to those of UFA-supplemented mitochondria. However, UFA-depletion has a marked effect on the ability of cytochromec to reactivate the NADH oxidase activity of cytochromec-depleted mitochondria.
    4. The efficiency of oxidative phosphorylation decreases progressively with the UFA content of the mitochondria, and oxidative phosphorylation is completely lost in mitochondria containing approximately 20% UFA.
    5. The incorporation of UFA into the lipids of UFA-depleted mitochondriain vivo results in a recoupling of oxidative phosphorylation. Recoupling is insensitive to both chloramphenicol and cycloheximide, indicating that all the proteins necessary for oxidative phosphorylation are present in UFA-depleted mitochondria, and that the less of oxidative phosphorylation is a purely lipid lesion.
    6. ATPase activity is apparently unaffected by UFA-depletion, but32Pi-ATP exchange activity is lost in mitochondria which have been extensively depleted in UFA.
    7. Valinomycin stimulates the respiration of UFA-supplemented mitochondria in media containing potassium, but has no effect on the respiration of UFA-depleted mitochondria, suggesting that active transport of potassium is lost as a result of UFA-depletion.
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    14.
    1. The inhibitory effects of CPTA, nicotine, DPA, and San 6706 on carotenogenesis in Myxococcus fulvus were investigated.
    2. The effects of CPTA, D-nicotine, and L-nicotine were very similar. The action of the drugs wasadditive. The cyclization was inhibited at low doses, the introduction of the hydroxyl group at C-1′ at higher doses. Lycopene accumulated at high drug concentration. The mode of action of the inhibitors is discussed.
    3. In a carotenoid mutant of M. fulvus a stimulation of the “7,8-dehydrogenase” by CPTA was observed.
    4. The specific carotenoid content of bacteria was increased by DPA due to an enhanced formation of phytoene. At low doses of DPA small amounts of an intermediate carotenoid glucoside ester, a 7,8-dihydro derivative, were detected.
    5. DPA was taken up by the plasma membrane. Quantitative removal of DPA by washing was not possible.
    6. San 6706 specifically and reversibly blocked the desaturation of phytoene.
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    15.
    1. Acute administration of ethanol (4 g/kg, i.p.) to mice inhibits the sequestration of calcium into endoplasmic reticulum-like organelles in synaptosomal membranes.
    2. Ethanol administration inhibits both Ca2+-stimulated adenosine triphosphate hydrolysis and ATP-dependent calcium uptake in the vesicles at time of loss of righting reflex.
    3. At recovery of righting reflex, the Ca2+-ATPase activity returns to normal levels, while the ATP-dependent uptake remains inhibited.
    4. The effect of ethanol is specific for the sequestration (active transport) of calcium since calcium binding to synaptic membranes is not altered.
    5. Alteration in mechanisms responsible for synaptosomal buffering of cytosolic Ca2+ levels by in vivo ethanol may contribute to altered transmitter release rates following ethanol adminstration.
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    16.
    1. A fully automated phototaxis monitoring device is described for measuring photo-topatactic responses of flagellated organisms.
    2. Photokinesis can be demonstrated in Chlamydomonas cells only after a dark period of about 72 hrs.
    3. Pre-darkening of a few hours duration raises the phototactic disposition, whereas pre-illumination has no significant effect.
    4. Circadian rhythms can be initiated by only one period of darkness or lower light intensity, whereas a period of higher intensity does not induce rhythms. The period length of the circadian rhythms is about 24 hrs.
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    17.
    U. H. Mane 《Hydrobiologia》1975,47(3-4):439-451
    1. The neutral red technique was employed to study the rate of filtration in Katelysia opima.
    2. The weight specific water filtration was found to be greater for younger clams compared to the older ones.
    3. The rate of water filtration increased with decreasing salinity.
    4. Water filtration was found to increase as temperature increased, reaching a maximum at 35°C. but then sharply decreasing at 39°C.
    5. Light had no significant effect on the rate of filtration.
    6. Suspended matter was found to affect the rate of water filtration.
    7. The rate of filtration was low at high pH and high in low pH.
    8. The rate of water filtration was found to be faster during high tide than during low tide.
    9. The presence of the parasitic crab, Pennotheris sp., in the mantle cavity of clams had a marked effect on the particle filtration.
    10. Accidental cut of the siphon tips had no effect on the rate of filtration.
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    18.
    In the absence of direct evidence concerning the nature of the early Earth environments, it is acceptable under the uniformitarian principle to attempt to define primitive habitats from modern procaryotic physiology. Combining the rock and fossil record with present phylogenetic reconstuctions, application of this paleoecological approach to the evolutionary biochemistry and physiology of nitrogen fixation and photosynthesis leads to several inferences about the nature of Archean environments:
    1. To stimulate nitrogenase evolution and avoid its repression, the activity of the NH 4 + ion was less than 10?3, and probably lower.
    2. To be consistent with a moderately protective ozone screen, while not also repressing nitrogenase activity, incursions of abiotic dissolved oxygen at levels in the range 10?1.2?10?3.5 PAL would have been acceptable.
    3. To induce the formation and activity of RuBP carboxylase, the pCO2 was less than 100 PAL.
    4. To support Photosystem I activity, sulfide concentrations of at least 10?4 M were present in the photic zone.
    5. To avoid a too-rapid oxidation of sulfide, the pH was probably between 6–7, where H2S exceeds HS?.
    Evolutionary ‘pressure’ to stimulate the later development of oxygenic photosynthesis (Photosystem II), would require several subsequent habitat modifications:
    1. Lowering the sulfide to < 10?4 M to inhibit Photosystem I.
    2. Raising the pH above neutral (HS? > H2S), to mediate more rapid oxidation of HS?.
    3. Maintaining either an illumination below 300–400 lux (to avoid photosynthetic O2 self-repression of nitrogen fixation), or an adequate local source of combined nitrogen (aNH 4 + > 10?4) to repress nitrogen fixation entirely.
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    19.
    1. Protease and amylase activity in the digestive system ofBarbus paludinosus Peters (Pisces, Cyprinidae) has been investigated.
    2. Chromatographic analysis showed seven amino acids to be present in both the anterior and posterior intestine. Only leucine, phenylalanine, valine, glycine and aspartic acid were positively identified.
    3. In the anterior intestine chromatography revealed two sugars, but only one in the posterior intestine which was identified as glucose.
    4. The pH of the intestinal fluid was found to be 5.8 and 7.8 for the fore and hind gut respectively, This correlates well with the enzyme pH optima found in in vitro experiments.
    5. Protease and amylase activity was found throughout the digestive tract. Maximum proteolytic activity being present in the anterior intestine. Amylase activity is similar in both regions of the gut.
    6. Correlation between the digestive enzymes and the fishes diet is briefly discussed.
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    20.
    1. Intracellular recording were obtained from P-cells of the LGN of the cat. The impulse trains of a single presynaptic retinal ganglion cell and the postsynaptic P-cell were separated by band-pass-filtering and subsequent amplitude discrimination.
    2. The rates of information and transinformation for the visual channel from the eye to a ganglion cell and to the connected P-cell were calculated. Input signals to the channel were trains of light flashes of different rate, luminance and spatial distribution.
    3. Transinformation was calculated without restrictive assumptions for the code.
    4. The transient behaviour of the system in response to a flash was fully considered for information calculations. Additionally, it was ensured that the state of the (adaptive) channel was considered correctly.
    5. Information theory was applied in an extended way. The time courses of information transfer were calculated for various flash stimuli and compared with each other.
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