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  • 1
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Analysis of the chemistry of calcified tissues has been suggested to be a source of useful information on the population structure and environmental history of fishes. We have investigated this approach as a means of determining the number of spawning areas and diversity of migration routes in the large pelagic scombrid, Thunnus maccoyii (southern bluefin tuna). Analysis was based on ontogenetic variation in the composition of sagittal otoliths, as measured using two probe microanalysers (wavelength dispersive electron probe microanalysis and proton-induced X-ray emission microanalysis), of 9 larvae collected on the single known spawning ground (NE Indian Ocean), of 29 juveniles caught at different points along the known migration routes (off western Australia, southern Australia, and South Africa), and of 14 adults caught in the high-seas fishery (off SE Australia). Fifteen elements were detected in T. maccoyii sagittae, but only six (Ca, Na, Sr, K, S, and Cl) were consistently present at concentrations above minimum detection limits. No attempt was made to measure the concentrations of C, N and O, which are assumed to also be present. Comparisons among different samples indicated that: (1) variation in the composition of the otolith primordium was unimodal and, generally, normally distributed; (2) this composition varied among specimens as a function of their size or, apparently, year-class; (3) individuals collected from widely separated locations did not differ clearly in the composition of the most recently deposited sections of their otoliths; and (4) all variation in the composition of adult otoliths was encompassed in the range of variation of juveniles collected along the major known migration route. These observations are consistent with the hypothesis of a single spawning area for T. maccoyii, but also indicate that the range of environmentally correlated variation in composition is too low to provide a robust test of the diversity of migration routes. It is not clear why this variation is so low, but we suspect that it reflects both the relative homogeneity of the pelagic environment and a weak effect of environmental factors on the concentration of elements present in otoliths at levels≳1 ppm.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 385 (1982), S. 109-132 
    ISSN: 0375-9474
    Keywords: Nuclear reactions
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 31 (1992), S. 1881-1889 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 32 (1993), S. 397-402 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 32 (1993), S. 403-408 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 69 (1998), S. 1075-1075 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A negative ion sputter source incorporating a microbeam Cs+ source intended for application in accelerator mass spectrometry (AMS) has been developed from a General Ionex HICONEX 834™ source. (HICONEX is a trade mark of High Voltage Engineering Europa.) The source is part of a microbeam AMS system, designed for in situ microanalysis of geological samples known as AUSTRALIS (AMS for UltraSensitive TRAce eLement and Isotopic Studies) recently developed at the Heavy Ion Analytical Facility laboratory. With requirements of precise beam positioning on mineralogical samples, a high magnification sample viewing system is a vital part of the source, enabling live observation of the sputtering process and visual tuning of the primary beam. Microbeam of Cs+ of 30 μm in diameter can be produced routinely with adequate intensity for a number of applications. The "screen" electrode in the secondary ion extraction system facilitates steering of the primary beam affected by the extraction field, back into the geometric center of the sample. The injector system includes high resolution electric and magnetic analyzers, improving the background suppression before injection into the accelerator. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 69 (1998), S. 1353-1358 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A negative ion sputter source incorporating a microbeam Cs+ source intended for application in accelerator mass spectrometry (AMS) has been developed from a General Ionex HICONEX 834™ source. (HICONEX is a trade mark of High Voltage Engineering Europa.) The source is part of a microbeam AMS system, designed for in situ microanalysis of geological samples known as AUSTRALIS (AMS for UltraSensitive TRAce eLement and Isotopic Studies) recently developed at the Heavy Ion Analytical Facility laboratory. With requirements of precise beam positioning on mineralogical samples, a high magnification sample viewing system is a vital part of the source, enabling live observation of the sputtering process and visual tuning of the primary beam. Microbeam of Cs+ of 30 μm in diameter can be produced routinely with adequate intensity for a number of applications. The "screen" electrode in the secondary ion extraction system facilitates steering of the primary beam affected by the extraction field, back into the geometric center of the sample. The injector system includes high resolution electric and magnetic analyzers, improving the background suppression before injection into the accelerator. © 1998 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Inst. and Methods in Physics Research, B 92 (1994), S. ix-x 
    ISSN: 0168-583X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Crystalline primary inclusions in diamonds from the Argyle and Ellendale lamproites have been analyzed for Mn, Ni, Cu, Zn, Ga, Pb, Rb, Sr, Y, Zr, Nb, Ta, Ba and Mo by proton microprobe. Eclogite-suite inclusions dominate at Argyle and occur in equal proportions with peridotite-suite inclusions at Ellendale. Eclogitic phases present include garnet, omphacitic clinopyroxene, coesite, rutile, kyanite and sulfide. Eclogitic clinopyroxenes are commonly rich in K and contain 300–1060 ppm Sr and 3–70 ppm Zr: K/Rb increases with K content up to 1400 at 0.7–1.1% K. Rutiles have high Zr and Nb contents with Zr/Nb=1.5–4 and Nb/Ta ∼16. Of the peridotite-suite inclusions, olivine commonly contains 〉 10 ppm Sr and Mo; Cr-pyropes are depleted in Sr, Y and Zr, and enriched in Ni, relative to eclogitic garnets. Eclogite-suite diamonds grew in host rocks that were depleted in Mn, Ni and Cr, and enriched in Sr, Zn, Cu, Ga and Ti, relative to Type I eclogite xenoliths from the Roberts Victor Mine. Crystallization temperatures of the eclogite-suite diamonds, as determined by coexisting garnet and clinopyroxene from single diamonds, range from ∼1085 to ∼1575° C. Log K D (C i cpx /C i gnt ) varies linearly with 1/T for Zr, Sr and Ga in most of the same samples. This supports the validity of the temperature estimates; Argyle eclogite-suite diamonds have grown over a T range ≥400° C. Comparison with data from eclogite xenoliths in kimberlites suggests that K D Sr and K D Zr are mainly T-dependent, while K D Ga may be both temperature-and pressuredependent. K D Ni , K D Cu and K D Zn show no T dependence in these samples. In several cases, significant major-and/or trace-element disequilibrium is observed between different grains of the same mineral, or between pyroxene and garnet, within single diamonds. This implies that these diamonds grew in an open system; inclusions trapped at different stages of growth record changes in major and trace-element composition occurring in the host rock. Diamond growth may have been controlled by a fluid flux which introduced or liberated carbon and modified the composition of the rock. The wide range of equilibration temperatures and the range of composition recorded in the inclusions of single diamonds suggest that a significant time interval was involved in diamond growth.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Contributions to mineralogy and petrology 103 (1989), S. 199-202 
    ISSN: 1432-0967
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Proton microprobe analyses of the minerals in garnet-peridotite xenoliths from kimberlites show that the partitioning of Ni between chrome pyrope garnet and olivine is strongly temperature(T)-dependent. The range of Ni contents in olivines is small relative to that in the analyzed garnets; a geothermometer therefore can be derived, based only on the Ni content of garnet. This allows estimation of T for single Cr-pyrope grains, such as the inclusions in diamonds, if these can be assumed to have equilibrated with olivine.
    Type of Medium: Electronic Resource
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