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  • Chemistry  (45)
  • Chloroplast  (2)
  • Nederland
  • Magnetism
  • 2005-2009  (2)
  • 1975-1979  (47)
  • 1
    facet.materialart.
    Unknown
    EIS-Nederland, Leiden
    Publication Date: 2024-01-12
    Keywords: Oestridae ; faunistiek ; Nederland ; Horzels
    Repository Name: National Museum of Natural History, Netherlands
    Type: info:eu-repo/semantics/bookPart
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  • 2
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    In:  Nederlandse Faunistische Mededelingen vol. 22, pp. 113-120
    Publication Date: 2024-01-12
    Description: Review of the genus Psilota in the Netherlands (Diptera: Syrphidae)\nA review of the genus Psilota in the Netherlands is presented. It is demonstrated that the genus\nis represented by a complex of two species, Psilota anthracina Meigen, 1822 and P. atra (Fall\xc3\xa9n,\n1817), as already indicated by Kassebeer. Both species can be separated using the key provided\nbelow. The interpretation of the species is exactly opposite to that in recent literature.\nUnfortunately, the holotype of P. atra Fall\xc3\xa9n was lost during transport. Therefore, we designate\na neotype, again a male from Sweden (fig. 6). Our interpretation of the species is based on this\nneotype and the description and pictures of P. anthracina by Meigen.\nThe habitats of both species in the Netherlands differ. Psilota atra is found near pine forest\nwhereas P. anthracina is found near deciduous forest. This seems to agree with the situation in\nthe surrounding countries, as far as we could establish. A key to both species is provided and the\nmale genitalia are illustrated.\nKey to the Dutch species\n1 Hind femur strongly thickened, about twice as broad as the mid femur. Female: posterior\n(convex) part of mesanepisternite with white hairs, abdomen predominantly lighthaired,\nthe 2nd tergite with conspicuous long white hairs in the frontal corners, 3rd tergite\npredominantly\nlight-haired; 3rd antennal segment about 2 times longer than high.\nMale: genitalia: epandrium distinctly elongated (fig. 4). . . . . . . . . . . . . Psilota atra\n- Hind femur only slightly thickened, at most 1.5 times as broad as the mid femur. Female:\nposterior (convex) part of mesanepisternite black-haired, abdomen more black haired,\nthe 2nd tergite without conspicuous long white hairs in the frontal corners, 3rd tergite\npredominantly\nblack-haired; 3rd antennal segment about 1.5 times longer than high.\nMale: genitalia: epandrium not elongated (fig. 5). . . . . . . . . . . . Psilota anthracina
    Keywords: Verspreiding ; Nederland ; Herkenning ; Determinatiesleutel ; Taxonomie ; Biotopen
    Repository Name: National Museum of Natural History, Netherlands
    Type: info:eu-repo/semantics/article
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Planta 137 (1977), S. 97-105 
    ISSN: 1432-2048
    Keywords: Chloroplast ; Ferredoxin-coding-site ; Nicotiana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ferredoxins were isolated and purified from leaves of different species of Nicotiana and Petunia and from spinach leaves. Their spectral properties, degree of homogeneity, and molecular weights were determined. The preparations were further analyzed by polyacrylamide gel electrophoresis of tryptic hydrolysates. This allowed us to distinguish between not only ferredoxins of Nicotiana, Petunia, and spinach, but even ferredoxins of various Nicotiana species. We used the differences in tryptic peptide compositions as phenotypic markers to study the mode of inheritance of chloroplast ferredoxin to see whether the coding site is in the chloroplast or in the nucleus. Analysis of the tryptic peptide composition of ferredoxin from different interspecific hybrids of Nicotiana showed that the characteristics of both parental ferredoxins were present. The results indicate that the primary structure of at least the male ferredoxin is coded for in the nucleus. In some of the hybrids the relative contribution of the male parent appeared to be low, suggesting that the female genome (presumably that part located in the plastome) exerted a dominating influence.
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  • 4
    ISSN: 1432-2048
    Keywords: Chloroplast ; Ferredoxin ; Immunofluorescence ; Nicotiana
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Antibodies were raised in rabbits against 2Fe−2S ferredoxin from N. tabacum L. The antibodies showed partial cross-reactivity in the double diffusion test with ferredoxins from Spinacia oleracea L., Petunia inflata Fries., P. axillaris Lam., Phaseolus vulgaris L., Chlamydomonas remhardii Dang. A complete cross-reaction was observed with ferredoxins from five other Nicotiana species, thus with this test it was impossible to discriminate between these ferredoxins. Therefore the following test was performed. Heterologous ferredoxin (i.e., ferredoxin other than from N. tabacum) was coupled covalently to Sepharose beads. Rabbit anti-N. tabacum-serum was then pre-incubated with this ferredoxin which resulted in complete abolition of cross-reactivity with free heterologous ferredoxin. However, the serum retained antibody activity against specific antigenic determinants of N. tabacum ferredoxin. When this serum was tested against ferredoxin purified from the hybrid: N. tabacum (♀)xN. glutinosa (♂) it gave a positive reaction. The relative content of maternal N. tabacum ferredoxin in the hybrid was estimated by using a fluorescent derivative of this specific antibody and estimating the cross-reactivity compared with that of artificial mixtures of pure N. tabacum and N. glutinosa ferredoxins. The hybrid contained 50% of maternal ferredoxin. This technique was also applied to ferredoxins of other species of Nicotiana and to the ferredoxin from the hybrid N. clevelandii (♀)xN. glutinosa (♂). We conclude that it provides a good test system for the study of the expression of chloroplast ferredoxin in Nicotiana hybrids in general.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 1735-1745 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Infrared spectroscopy was used for the determination of the base-pairing content of four specific tRNAs in deuterium oxide solution. Infrared spectra were obtained in the 1750-1550 cm-1 region at various temperatures ranging from about 15 to 90°C. Melting curves were constructed by plotting the molar extinction coefficient at ν = 1657 cm-1 versus temperature. These transition curves enabled us to determine the ranges of temperature which correspond to the ordered (partially double-stranded) or randomly coiled structure of the tRNA. For a set of wavenumbers the extinction coefficients at these temperatures were used for the calculation of the base-pairing content. The procedure employed here is based on a method described earlier by Thomas [(1969) Biopolymers 7, 325-334]. For the conditions selected for this investigation (Mg2+-free D2O-buffer; 0.01M tris-DCl, 0.015M NaCl, pD 7.5) the results of this determination agree within the limits of errors with the number of base pairs predicted by the cloverleaf model.
    Additional Material: 7 Ill.
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  • 6
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Organic radicals were produced in the tensides C16H33(OCH2CH2)21OH and C14H29(OCH2CH2)3-SO3Na in aqueous solutions using a short pulse of high energy electrons. The radicals were formed by OH attack on the (OCH2CH2)x-parts of the tensides. The decay of the 250nm absorption of the radicals was recorded at different initial radical concentrations and tenside concentrations. Several radicals could be produced in one micelle. Radicals formed in the same micelle decay within microseconds or faster. The half life time τ1 in a micelle carrying two radicals is 2,0·10-6 s for C16H33(OCH2CH2)21 OH and less than 6·10-7 s for C14H29(OCH2CH2)3SO3Na. A model for intramicellar radical-radical reactions is proposed according to which the rate is faster in tensides of high critical micelle concentration. Single radicals in micelles of C16H33(OCH2CH2)21OH can deactivate each other without leaving the micelles. This intermicellar reaction is discussed in terms of the rate of diffusion-controlled micelle-micelle encounters, an encounter time of 7·10-8s, and the above time τ1 for intramicellar reaction. The observed rate constant 2k of intermicellar reaction is 3,5·106 mol-1·l·s-1. At low tenside concentrations, the bimolecular rate constant increases since more single tenside radicals are present in solution. They react rapidly (ca. 108 mol-1·l·s-1) with radicals in micelles. Single radicals in C14H33(OCH2CH2)3-SO3Na micelles cannot directly react with each other because of the Coulombic repulsion between two anionic micelles. Reaction occurs after the exit of a tenside radical from its micelle, the rate of which depends on the micellar equilibrium Mn⇄Mn-1+M (M: tenside molecule; n: agglomeration number of micelle). A single radical in solution reacts with a single radical in a micelle with 2k = 1,0·108 mol-1·l·s-1 and with another single radical in solution with 4,0·107 mol-1·l·s-1.γ-Irradiation of both tensides in aqueous solution leads to slight increases in viscosity, followed by turbidity beyond the “gel dose” and phase separation. These effects are explained in terms of crosslinking of tenside molecules. Formation of a large network requires bridges between all participating tenside molecules (not only bridges between micelles).
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 1 (1978), S. 97-97 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography ; Structure and relation of polyhalogenated aromatics ; discussed ; Silica gel/aluminium oxide compared ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 8
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary, glass ; Separation of polychloro biphenyls ; Separation of organochlorine pesticides ; Splitless automated injection ; Residue level ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complicated PCB mixtures can be separated in individual compounds using glass capillary gas chromatography, (GC)2. Depending on extraction and clean-up procedure it is also possible to separate and determine organochlorine pesticides at the same time.This (GC)2 technique can be used to determine the contents of individual chlorinated biphenyls in milk products and animal feedstuffs and in the analysis of complicated extracts of soil and vegetable material.Practical aspects concerning connection of the capillary, automatic splitless injection, repeatability of the retention time, quality of the column with respect to separation and adsorption and degradation of DDT are discussed.The detection of individual chlorinated biphenyls is possible at the ppb level in fats and vegetable materials, using an extraction and clean-up procedure, based on saponification of the sample.Preliminary results for milk, obtained from several areas, are shown.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 9 (1978), S. 406-413 
    ISSN: 0933-5137
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Form and Mechanisms of Cracks and Fractures Caused by Simultaneous Corrosive and Dynamic Stress under Various FrequenciesDistinction of crack nucleation and crack propagation under variable frequencies and electrolytic corrosion. Relationship between crack nucleation and frequency due to differing sliding mechanisms. Crack propagation under decreasing frequencies causes transition from corrosion fatigue to cyclic stress corrosion cracking and finally stress corrosion cracking can be observed. Coordination of that transition with the increasing influence of the KISCC-value as determinant of the crack propagation.The influence of frequency on high temperature materals in hot gas atmosphere is mainly determined by creep mechanisms during top-load phase and the gas-metal-reactions. Accordingly the life time increases with growing load frequency.
    Notes: Anrißphase und Phase des Rißfortschritts bei der Betrachtung der Frequenzabhängigkeit unter elektrolytischer Korrosion. Abhängigkeit der Anrißphase von der Frequenz infolge unterschiedlicher Gleitmechanismen. Beim Rißfortschritt erfolgt mit sinkender Frequenz Übergang von Schwingungsrißkorrosion zu zyklischer Spannungsrißkorrosion und schließlich zu Spannungsrißkorrosion. Zuordnung dieses Übergangs zum zunehmenden Einfluß des KISCC-Wertes als Bestimmungsgröße für den Bruchvorgang.Frequenzabhängigkeit bei Hochtemperaturwerkstoffen in Heißgasatmosphäre im wesentlichen bestimmt durch Kriechvorgänge bei Einwirkung der Oberlast und zeitabhängige Gas-Metall-Reaktionen. Entsprechend verlängern sich die Standzeiten mit zunehmender Belastungsfrequenz.
    Additional Material: 16 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 2 (1979), S. 11-14 
    ISSN: 0935-6304
    Keywords: Liquid chromatography ; Fluorescence ; Ion-pair extraction ; Amines ; Post-column reaction ; Auto-analyser ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detection system is described which is based on fluorescent ion-pair formation between tertiary amine drugs and dimethoxyanthracene sulphonate. A dynamic micro-extraction principle is then used to isolate the ion-pairs from the excess reagent. The band broadening of this extraction detector was kept below 20% using standard auto-analyser equipment. With the enhanced selectivity and sensitivity of this approach it was possible to analyse chloropheniramine in urine at ppb concentrations using a pre-column clean-up trace enrichment step.
    Additional Material: 5 Ill.
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