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  • Articles  (1,460)
  • Data  (2)
  • Inorganic Chemistry  (1,459)
  • earthquakes
  • velocity
  • 1980-1984  (1,462)
  • 1983  (703)
  • 1980  (759)
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  • 1980-1984  (1,462)
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  • 1
    Publication Date: 2023-05-12
    Description: Abstract
    Description: Sodankylä geophysical observatory (SGO) has operated in Sodankylä in northern Finland since 1913. SGO was originally founded by the Finnish Academy of Science and Letters. Now it takes care of national and international duties studying the space and geoenvironment as an independent research organisation in the University of Oulu. SGO performs long-term measurements, builds instruments, innovates and maintains domestic and international measurements, and performs research from these measurements. The seismic observations at SGO started in Sodankylä 1956. In 2005-2006 SGO seismic stations were updated to broadband instrumentation and connected to GEOFON data center. Today, the number of seismic stations has increased to 9. The stations have Streckeisen STS-2 or Nanometrics Trillium PA/PH broadband sensors. 3 of the stations are so called Posthole stations located in borehole 7-20 m below surface. The rest of the stations are located on the surface or in a more traditional type of vault. Data acquisition systems are either Earth Data PS6-24 digitisers and PC with Seiscomp or Nanometrics Centaurs. The continuous wave form data is collected at 100 Hz sampling frequency. The VH, LH and BH channel data is available from GEOFON data center and the 100Hz HH data from SGO by request. Further information about instrumentation can be found at the Institute’s web site (https://www.sgo.fi/). Waveform data are available from the GEOFON data centre, under network code FN, and arefully open.
    Keywords: geophysics ; seismology ; seismic noise ; earthquakes ; induced ; seismic hazard ; broad band ; velocity ; acceleration ; displacement ; Broadband seismic waveforms ; Seismic monitoring ; EARTH SCIENCE 〉 SOLID EARTH 〉 TECTONICS 〉 EARTHQUAKES ; In Situ/Laboratory Instruments 〉 Magnetic/Motion Sensors 〉 Seismometers ; In Situ Land-based Platforms 〉 GEOPHYSICAL STATIONS/NETWORKS ; In Situ Land-based Platforms 〉 GEOPHYSICAL STATIONS/NETWORKS 〉 SEISMOLOGICAL STATIONS
    Type: Dataset , Seismic Network
    Format: ~300G
    Format: .mseed
    Format: XML
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  • 2
    Publication Date: 2023-02-08
    Description: Abstract
    Description: The Institute of Seismology, University of Helsinki (ISUH) was founded in 1961 as a response to the growing public concern for environmental hazards caused by nuclear weapon testing. Since then ISUH has been responsible for seismic monitoring in Finland. The current mandate covers government regulator duties in seismic hazard mitigation and nuclear test ban treaty verification, observatory activities and operation of the Finnish National Seismic Network (FNSN) as well as research and teaching of seismology at the University of Helsinki.The first seismograph station of Finland was installed at the premises of the Department of Physics, University of Helsinki in 1924. However, the mechanical Mainka seismographs had low magnification and thus the recordings were of little practical value for the study of local seismicity. The first short-period seismographs were set up between 1956 and 1963. The next significant upgrade of FNSN occurred during the late 1970’s when digital tripartite arrays in southern and central Finland became fully operational, allowing for systematic use of instrumental detection, location and magnitude determination methods. By the end of the 1990’s, the entire network was operating using digital telemetric or dial-up methods. The FNSN has expanded significantly during the 21st Century. It comprises now 36 permanent stations. Most of the stations have Streckeisen STS-2, Nanometrics Trillium (Compact/P/PA/QA) or Guralp CMG-3T broad band sensors. Some Teledyne-Geotech S13/GS13 short period sensors are also in use. Data acquisition systems are a combination of Earth Data PS6-24 digitizers and PC with Seiscomp/Seedlink software or Nanometrics Centaurs. The stations are connected to the ISUH with Seedlink via Internet and provide continuous waveform data at 40 Hz (array) or 100-250 Hz sampling frequency. Further information about instrumentation can be found at the Institute’s web site (www.seismo.helsinki.fi). Waveform data are available from the GEOFON data centre, under network code HE, and arefully open.
    Keywords: geophysics ; seismology ; seismic noise ; earthquakes ; induced ; seismic hazard ; broad band ; velocity ; acceleration ; displacement ; Monitoring system ; Seismological stations ; In Situ/Laboratory Instruments 〉 Magnetic/Motion Sensors 〉 Seismometers ; In Situ Land-based Platforms 〉 GEOPHYSICAL STATIONS/NETWORKS
    Type: Dataset , Seismic Network
    Format: ~300G
    Format: .mseed
    Format: XML
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Hydrobiologia 106 (1983), S. 157-168 
    ISSN: 1573-5117
    Keywords: benthic macroinvertebrates ; instream flow management ; depth ; velocity ; substrate ; microhabitat preferences
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Estimates of numbers, biomass, and diversity of benthic macroinvertebrates were made quarterly over a two-year period to investigate microhabitat preferences. Although biomass of most taxa was significantly different among sampling times, physical factors also appeared to be important in determining abundance of many taxa. Optimum depth, velocity, substrate type, and turbulence were determined for major taxa. Optimum conditions for diversity appeared to be 34 cm depth, 60 cm s−1 velocity, and rubble and boulder substrate type. Habitat preference functions were derived for several taxa based on significant polynomial regressions of biomass on depth, velocity, substrate, and Froude number (turbulence). The relationship between abundance and physical habitat conditions was tested by using the product of the preference factors (range: 0–1) for depth, velocity and substrate type as a measure of habitat suitability (joint preference factor). There were significant correlations between biomass [transformed by loge (x + 1)] of 10 benthic species and the joint preference factor. The joint preference factors accounted for from 11 to 61% of the variation of biomass of the 10 benthic species. The intercepts of the relationships between biomass of individual species and the joint preference factor were not significantly different from zero for any species. Therefore, the joint preference factors appear to be valid indicators of biomass. The preference functions have utility in habitat assessment studies, specifically with regard to minimum instream flow determinations.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 800-805 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2-Disubstituted 1,3-Dithianes from β-Dicarbonyl Compounds1,3-Dicarbonyl compounds 2 can be condensed with 1,3-propanedithiol (1) to yield 2,2-disubstituted 1,3-dithianes 3 which are remarkably stable in contrast to analogous open-chain thioacetals 6. Compounds with alkoxycarbonyl functions are easily hydrolysed to the corresponding carboxylic acids 11 which by further esterification with alkanols 12 yield estermodified 1,3-dithianes 3. All new compounds are characterized by 13C NMR spectroscopy.
    Additional Material: 3 Tab.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 806-807 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Perchloro-2-methylene-2H-pyranThe synthesis of the title compound 4 is described. 4 is thermally and chemically very stable.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980), S. 808-810 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Anchimerically Enhanced Homolyses, V. Fluoride Ion Catalysed Rearrangements of Benzyl 9-(Trimethylgermyl)-9-fluorenyl EtherThe thermal rearrangement (homolysis) of the germanium compound 1d into 4d is considerably slower than that of the analogous Si compound 1c. Thus, a correlation is suggested between the velocity of the rearrangement and the strength of the new bond to oxygen. The rearrangement 1d→4d is also induced by fluoride ions at room temperature.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 113 (1980) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 55-65 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cycloaddition Reactions of Heterocumulenes, XXVI. Cycloadducts from Aryl Isothiocyanates and 2,2-Disubstituted EnaminesAryl isothiocyanates 1 react with enamines 2 to give two types of 2:1 cycloadducts. Below 50°C, 1a - g and 2 give rise to 6-imino-1,3-thiazine-2-thiones 5, the constitutions of which are proved by an X-ray analysis of 5c. Above 50°C or starting from 4-nitrophenyl isothiocyanate (1h),2,4-dithiouracils 6 are formed. 1:1 cycloadducts of the reactants are detected spectroscopically; on workup, they hydrolyze to give 2-formylthiopropionanilides 9.
    Notes: Arylisothiocyanate 1 und Enamine 2 reagieren zu zwei Typen von 2:1-Cycloaddukten. Unterhalb von 50°C entstehen aus 1a - g und 2 6-Imino-1,3-thiazin-2-thione 5, deren Konstitution durch die Röntgenstrukturanalyse von 5c bewiesen wurde. Oberhalb 50°C oder aus 4-Nitrophenylisothio-cyanat (1h) bilden sich 2,4-Dithiouracile 6. 1:1-Cycloaddukte der Reaktanten lassen sich spektroskopisch nachweisen; bei der Aufarbeitung hydrolysieren sie zu 2-Formylthiopropionaniliden 9.
    Additional Material: 3 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 116 (1983), S. 544-548 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal and Molecular Structure of the Anthraquinonophane [2.0.0](1,4)Benzeno(1,8)anthraquinono(1,4)benzenophaneBoth phenylene rings in the [5.2]paracyclophane subunit of the anthraquinonophane [2.0.0](1,4)benzeno(1,8)anthraquinono(1,4)benzenophane (1) are tilted by 37.6°. They show a boat-like deformation. The carbonyl group pointing towards the interior of the molecule interacts with the paracyclophane system. From this a strong boat-like deformation of the quinone ring of the anthraquinone moiety results.
    Notes: Die beiden Phenylenringe in der [5.2]Paracyclophan-Untereinheit des [2.0.0](1,4)Benzeno(1,8)-anthrachinono(1,4)benzenophans (1) sind um 37.6° gegeneinander geneigt und wannenförmig deformiert. Die Wechselwirkungen der ins Molekülinnere zeigenden Carbonylgruppe mit dem Paracyclophan-System verursachen eine starke wannenförmige Deformation des Chinonringes in der Anthrachinon-Einheit.
    Additional Material: 2 Tab.
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  • 10
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Four- and Five-membered Phosphorus Heterocycles, 55. 1,2,4-Diazaphospholo-[1,2,3]diazaphospholes - Preparation by Phosphaalkene + Nitrilimine Cycloaddition, Decomposition by Nitrile Elimination, and Structural Comparison of Addend and Adduct2,5-Dimethyl-1,2,3-diazaphosphole (1a) reacts with N-Phenylbenzohydrazonoyl chloride (6a) and a base in a sequence of nitrilimine cycloaddition, benzonitrile elimination, and another cycloaddition to give in the second step the 4-anilino derivative 7 of 1a, in the first and third step the 7a-unsubstituted and 7a-anilino-substituted title compound, 3a and 8, respectively. - As shown by the molecular structures, determined by X-ray analysis, there is a 6 π delocalization in 7 which is lost in 8 with remarkably little geometrical change at the phosphorus. - Other nitrilimines add to 1a in the same direction, that is with PC- and CN-bond formation.
    Notes: 2,5-Dimethyl-1,2,3-diazaphosphol (1a) reagiert mit N-Phenylbenzohydrazonoylchlorid (6a) und einer Base in einer Folge von Nitrilimin-Cycloaddition, Benzonitril-Eliminierung und neuerlicher Cycloaddition. In der zweiten Stufe bilden sich dabei das 4-Anilinoderivat 7 von 1a, in der ersten und dritten Stufe entstehen die 7a-unsubstituierte und 7a-anilinosubstituierte Titelverbindung, 3a bzw. 8. - Die röntgenographisch bestimmten Molekülstrukturen zeigen für den Übergang von 7 in 8 die Aufhebung einer 6 π-Delokalisierung bei nur geringen geometrischen Veränderungen am Phosphor. - Auch andere Nitrilimine addieren sich an 1a in gleicher Richtung, also unter PC- und CN-Verknüpfung.
    Additional Material: 6 Tab.
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