不同生物量的乳酸杆菌对对虾养殖池3种常见优势微藻的影响

在实验室条件下,分别把对虾养殖池常见优势种——微绿球藻（Nannochloropsis oculata）、隐藻（Cryptomonas erosa）和颤藻（Oscillatoria）与乳酸杆菌（Lactobacillusspp.）在对虾养殖水体中共同培养,研究不同生物量的乳酸杆菌对3种微藻的影响.实验分4组,乳酸杆菌分C1（10^3cells/cm^3）组、C2（10^4cells/cm^3）组、C3（10^5cells/cm^3）组、C4（10^6cells/cm^3）组四个浓度.结果表明：不同生物量的乳酸杆菌对不同微藻的影响有很大差异.C1（10^3cells/cm^3）乳酸杆菌对微绿球藻的生长没有明显的影响,对隐藻和颤藻生长有明显的抑制作用.C2（10^4cells/cm^3）乳酸杆菌对微绿球藻和隐藻生长有明显的促进作用,对颤藻生长有明显的抑制作用.C3（10^5cells/cm^3）乳酸杆菌对隐藻生长有明显的抑制作用,对颤藻的生长有明显的促进作用.C4（10^6cells/cm^3）乳酸杆菌对微绿球藻和颤藻生长有较明显的促进作用,对隐藻生长有微弱的抑制作用.无论是抑制作用还是促进作用,这种作用都随实验时间的延长而减弱.     

Development of an Enzyme Immunoassay for the Analysis of the Atrazine Metabolite Hydroxyatrazine Entwicklung eines Enzymimmunoassays zur Analyse des Atrazin-Metaboliten Hydroxyatrazin

A highly sensitive and specific enzyme immunoassay (EIA) is described for the detection of the atrazine metabolite hydroxyatrazine. Polyclonal antibodies were raised in rabbits by immunization with a hapten-bovine serum albumin (BSA) conjugate containing 8 hapten residues per molecule of BSA. An EIA with a horseradish peroxidase (HRP) hapten tracer was optimized in microtitre plates. A concentration of 50% B/B₀ was found at 0.10 μg/L for hydroxyatrazine. A limit of determination for hydroxyatrazine was reached at approximately 0.01 μg/L, i.e. well below the maximum concentration permitted by the EU guidelines for drinking water and the drinking water ordinance of the FRG. The assay did not require concentration or clean-up steps for drinking water or ground water samples. Validation experiments confirmed a good accuracy and precision. Hydroxyatrazine is reported to be the main atrazine metabolite found in soil samples. As organic solvents are usually employed for soil extraction, the influence of methanol as representative organic solvent on the assay was examined. Up to a concentration of 5% (v/v) methanol, the organic solvent did not affect the assay.     

A Screening Procedure for Heavy Metals in Soil Extracts by Alcohol Dehydrogenase and Urease Inhibition Eine Screening-Methode für Schwermetalle in Extrakten aus Bodenproben,basierend auf der Inhibierung der Enzyme Alkoholdehydrogenase und Urease

A screening method for heavy metals in aqueous extracts of soil is presented which is based on inhibition of the enzymes urease and alcohol dehydrogenase. The method is suitable to detect cupric and mercury ions in concentrations below 0.01 mg/L and several other heavy metal ions in 1000 fold higher concentration. It is shown that the test may be used for screening of mercury ion concentrations exceeding 0.03 mg/L in aqueous solution when copper chelators are added to the test system. The usefulness of the presented tests to detect heavy metals eluted from soil was verified with samples from ore mining waste. The concentration of copper, lead, and zinc eluted from these samples to different amount was determined by atomic absorption spectrometry and was in good agreement with the enzyme inhibition data obtained with these samples.     

Entwicklung eines Enzymimmunoassays zum Nachweis des Herbizids Mecoprop in Trink- und Grundwasser auf der Basis von Antikörpern aus den Eiern von Legehennen

Development of an Enzyme Immunoassay for the Detection of Mecoprop in Drinking Water and Groundwater Based on Antibodies Raised in Chicken Egg Yolk Antibodies against mecoprop were isolated from egg yolk of immunized hens and were used for the development of an enzyme-linked immunosorbent assay. We tested assay parameters (pH and concentration of buffer, incubation temperature, kind of enzyme tracer) to optimize the standard curve for mecoprop. By decreasing the pH, the detection limit was reached at a concentration of 0.35 μg/L mecoprop. The concentration for 50% inhibition (50% B/B₀) was 2.8 μg/L. Dichlorprop and the methyl esters of both mecoprop and dichlorprop showed high crossreactivity (165%, 400% and 233%). Antibodies against mecoprop separated from egg yolk were compared to antibodies raised in rabbit for both sensitivity and specificity. Chicken immunoglobulins were found to be less sensitive and specific than the mammalian IgG's.     

The Influence of Oxalate on Fe-Catalyzed S(IV) Oxidation by Oxygen in Aqueous Solution

This study demonstrates that oxalate has a strong inhibiting effect onFe-catalyzed S(IV) oxidation by oxygen in aqueous solution. While thepseudo-first order rate constant of S(IV) oxidation was determined to be1.6 × 10³ M^-1 s^-1 in experimentswithout oxalate, the oxidation of S(IV) was totally inhibited at a molarconcentration ratio of iron:oxalate = 1:5 at an oxalate concentration of 4M. Under these conditions, the Fe(II)/Fe(III) ratio remained nearlyconstant during the observed reaction time. The determined rate constants wereindependent of the initial oxidation state of iron. However, with increasingconcentrations of oxalate, a longer induction period is observed forexperiments with iron initially in the Fe(II) oxidation state.     

Seasonal growth in brown trout in two New Zealand streams

Brown trout Salmo trutta Linn, were marked with individual tags and recaptured throughout a year in two small Canterbury streams. The growth recorded showed a marked seasonal variation which differed in pattern in the two streams. There was a considerable difference in the growth rate between the two populations and fish transferred from the slow‐growth stream to the faster‐growth stream showed an immediate response to the change.     

pH值对适于页岩气储层的SDBS压裂液性能的影响研究

在低渗、低孔隙率页岩气储层压裂改造过程中,压裂液体系的pH值直接影响地层中的造缝、稳缝效果。pH值对阴离子表面活性剂压裂液的粘度、表面张力和页岩膨胀抑制性影响很大。通过改变阴离子表面活性剂的浓度,测定了在不同pH值条件下压裂液体系基本性能的变化。研究表明：SDBS压裂液体系的粘度随着pH值的增加先增大后减小,在pH值=9时达到最大;体系在pH值=5时降低体系表面张力的能力最好;页岩的膨胀量随着pH值的增大逐渐增大,在pH=7时膨胀量最大,且随着pH值的进一步增大,页岩膨胀量先减小后增大,在pH值=9时膨胀量最小;当体系的pH值一定时,SDBS在临界胶束浓度状态能够最大程度抑制页岩的膨胀。从化学微观角度上分析了pH值对SDBS压裂液性能的影响,有利于SDBS压裂液体系配方优化。     

Tracing of Peroxidase Activity in Humic Lake Water

An enzyme assay was developed for studies on peroxidase activities in humic lake water. 3,4-Dimethoxybenzyl alcohol (veratryl alcohol, VeraOH) was used as tracer substrate, and peroxidase (EC 1.11.1.7) activity was measured by high-performance liquid chromatography. The chemical stability of VeraOH and its application as peroxidase substrate was tested under light and dark conditions, different hydrogen peroxide (H₂O₂) concentrations and humic matter contents. VeraOH was stable under low UV radiation at in situ conditions in lake water (<0.010...0.25 kJ m^–2 d^–1), laboratory conditions (<0.05...0.30 kJ m^–2 d^–1), and low (1...100 μM) H₂O₂ concentrations. However, peroxides oxidized VeraOH above 1...10 mM H₂O₂ concentration in sterile Millipore-Q and humic lake water. Dark incubations showed little VeraOH oxidation products. The developed peroxidase assay was tested in the growth medium of Phanerochaete chrysosporium and a bacteria isolate (P.M.D. 20.4.3.1) from mesohumic lake Pääjärvi. Peroxidase activities were also measured in natural microbial communities under standard laboratory and under in situ conditions in humic lake water. Incubation times of about 5 to 12 days were usually needed to record significant (P < 0.05) peroxidase activities, in lake waters. In situ peroxidase activities varied in pelagial surface water (0...0.5 m) on a seasonal scale between 74 nmol L^–1 h^–1 and 273 nmol L^–1 (mean: 176 nmol L^–1 h^–1) and within the water column between 110 nmol L^–1 h^–1 and 800 nmol L^–1 h^–1 (mean: 500 nmol L^–1 h^–1) in polyhumic lake Mekkojärvi.