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  • 1
    Series available for loan
    Series available for loan
    Washington, DC : United States Gov. Print. Off.
    Associated volumes
    Call number: SR 90.0002(1044-I)
    In: Professional paper
    Type of Medium: Series available for loan
    Pages: IV, I-47 S. + 1 pl.
    Series Statement: U.S. Geological Survey professional paper 1044-I
    Language: English
    Location: Lower compact magazine
    Branch Library: GFZ Library
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 30 (1991), S. 8512-8517 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 9527-9529 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present the resonance Raman and Raman excitation profile of mass-selected zirconium trimers in argon matrices. In the Raman spectra, two fundamentals and one overtone are observed. Average Raman shifts, along with standard deviations (in parentheses) are 176.7 (13) cm−1 (ν2), 258.0 (12) cm−1 (ν1), and 516.1 (8) cm−1 (2ν1). The ratio of the frequencies of the two lowest lines (ν1/ν2) is 1.46, which is very close to (square root of)2. This is indicative of a symmetrical equilateral geometry (D3h). In such a case we expect two normal frequencies, one for a totally symmetric stretch of symmetry a′1 (ν1) and a doubly degenerate bend of symmetry e′(ν2). The Raman excitation profiles of the ν1(a′1) line shows two broad maxima: one near 491 nm and the other near 614 nm. The ν2 (e′) profile shows a broad region of intensity only near 614 nm. With the aid of theory we assign the 614 nm band to be 1A′1−1E′ (x,y polarized) while the 491 nm band must be 1A′1−1A″2 (z polarized). © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 9280-9282 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report absorption and Raman spectra for cobalt dimers in an argon matrix prepared by the mass-selected ion deposition technique. A weak dimer absorption band was found between 425 and 485 nm. Resonance Raman spectra (obtained by exciting between 457.9–488.0 nm) give ωe‘= 296.8(54) cm−1 with ωexe‘ = 2.2(8) cm−1. The dicobalt data are discussed in terms of results from recent photodetachment experiments which suggest a changeover from d–d bonding to s–s bonding along the series Fe2→Cu2. © 1994 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 106 (1997), S. 8339-8343 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report on the optical, resonance Raman, and excitation profile spectra of mass selected hafnium trimers in argon matrices at 14 K. The absorption spectrum consists of four overlapping transitions in the range 605–620 nm. The Raman spectrum is too complex to be attributed to a single ground state. We may explain the observed spectrum by assuming five low-lying excited states A, B, C, D, and E at 319.0, 413.4, 609.6, 642.8 (weak), and 785.4 cm−1, respectively. The ground (X) state shows complex structure which may be interpreted as the result of a strong, but linear Jahn–Teller effect. Evidence is obtained for two pseudo-rotational progressions having states of vibronic angular momentum of j=±1/2,...,±7/2 based upon a1′ normal frequencies of 142.8 and 278.1 cm−1. This indicates a fluxional ground state with E symmetry in the D3h limit. No such effects are apparent in the low-lying excited states, although a1′ modes of 143–152 cm−1 are observed and in some cases geometrical information may be inferred. The A state (319.0 cm−1) is geometrically an equilateral triangle (D3h symmetry). The B state (413.4 cm−1) shows an a1′ vibration, but without an observed nontotally symmetric mode no geometrical information can be obtained. The C state (609.6 cm−1) shows only a nontotally symmetric mode at 116.7 cm−1, while the D state (642.8 cm−1) and the E state (785.4 cm−1) both appear to have D3h symmetry. Raman excitation profiles appear as several distinct types and correlate well with the four absorption bands at 606, 610, 615, and 619 nm. © 1997 American Institute of Physics.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 3289-3292 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have examined both the absorption and resonance Raman spectra of mass-selected Ta tetramers. The tetramers are produced in a sputtering source and mass filtered with a Wien filter, then neutralized and deposited in an Ar matrix at low temperatures. The absorption spectrum indicates two broad transitions, one in the red at 768 nm and another to the blue at 532 nm. Raman resonances could be excited in both regions giving three distinct fundamental frequencies at 270.2(1) cm−1, 185.1(1) cm−1, and 130.6(2) cm−1. The lowest vibration shows a long progression (up to seven overtones) with alternating separations of 135 cm−1 and 126 cm−1, indicative of a weak Jahn–Teller effect in the tetramer ground state. This, along with the observation that the fundamental frequency ratios are close to 2:(square root of)2:1 indicate that the molecule has a tetrahedral ground state geometry with an electronic E state symmetry. The appearance of three fundamentals in the resonance Raman spectrum indicates that both excited states corresponding to the observed absorption bands arise from severely distorted T electronic states. © 1995 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 5355-5357 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The absorption (scattering depletion) spectrum and Raman spectra for Nb3 in an argon matrix prepared by the mass selected ion deposition technique have been obtained. The absorption spectrum in the visible region shows three overlapping transitions, centered at 20 300 cm−1 (A), 18 800 cm−1 (B), and 17 000 cm−1 (C), respectively. Resonance Raman spectra obtained with excitation into these bands display two distinct fundamental frequencies at 227.4±2.9(e′) and 334.9±2.8(a1′) cm−1 which indicate that the ground state of the Nb3 molecule has a nearly equilateral triangular geometry (D3h). The fr (bond stretch) and frr (stretch–stretch interaction) force constants for Nb3 are determined to be 1.95 and 0.05 mdyn/A(ring), respectively. The Raman excitation profiles bear a strong resemblance to the triniobium absorption spectrum, but the peaks seem more closely spaced than the absorption spectrum. Both a1′ and e′ vibration are observed with the same intensity near the peak A, while the a1′ vibration dominates the profile at the peak B. Neither displays much intensity near the peak C. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 3420-3422 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The absorption and Raman spectra for nickel dimers in an argon matrix prepared by the mass-selected ion deposition technique have been measured. A weak dimer absorption band is centered around 480 nm. Resonance Raman spectra obtained from exciting into the dimer 480 nm band show a vibrational progression for which ωe=259.2±3.0 cm−1 with ωexe=1.9±0.7 cm−1. The dinickel Raman spectra are discussed in terms of isotopic shifts, as well as the changeover from d–d bonding to s–s bonding along the series Fe2→Cu2. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Aquaculture research 36 (2005), S. 0 
    ISSN: 1365-2109
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Species of the family Clionaidae (Porifera: Demospongiae) that excavate shell of the silver-lip pearl oyster, Pinctada maxima, in north Western and Northern Australia are described. Two species belong to the genus Cliona and one species to the closely related genus Pione. Cliona orientalis has only recently been reported from Australia in living and dead coral on the Great Barrier Reef, and this is the first report of this species from north Western and Northern Australia. Cliona dissimilis is reported from Australia for the first time. Pione velans was first described from Shark Bay, Western Australia and this study extends its distribution from Albany, south Western Australia to Port Bremer in the Northern Territory. The most common species found was C. dissimilis. Pione velans and C. orientalis were also present, although the latter species was rare. Cliona dissimilis and P. velans were found to be sexually reproductive in some shells with specimens of C. dissimilis with oocytes in May and P. velans in September 1999. Egg development was synchronous, indicating that the sponges were oviparous and would broadcast gametes in a spawning event.
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  • 10
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    Unknown
    Detroit, Mich. : Periodicals Archive Online (PAO)
    Technology and Culture. 17:4 (1976:Oct.) 776 
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