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  • 1990-1994  (5)
  • 1980-1984  (2)
  • Analytical Chemistry and Spectroscopy  (5)
  • One-male units  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Cycle synchrony and probability of conception in female hamadryas baboonsPapio hamadryas (1994)
    Springer
    Behavioral ecology and sociobiology 35 (1994), S. 175-183 
    Details
    ISSN: 1432-0762
    Keywords: Papio hamadryas ; One-male units ; Probability of conception ; Synchrony of estrus ; Female-female competition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We investigated the factors affecting conception in a captive population ofPapio hamadryas. We collected data on reproductive states from 16 females over 12 years. Probability of conception was related to the outcome of the immediately preceding pregnancy and the fate of the preceding offspring. After abortions or when an infant survived more than 6 months, a female needed more cycles to conceive than when an infant died within the first 6 months post partum. The degree of estrus synchrony within, but not between, one-male units influenced the probability of conception. Females experiencing conceptive estrus showed less synchrony than those experiencing nonconceptive estrus. The number of females simultaneously in estrus within a one-male unit was negatively correlated with the probability of conception. Within our captive population, group size and male and female age had no influence on the probability of conception. The results indicate that sperm may be a limited resource in the one-male reproductive units of hamadryas baboons. Female-female competition for conception may exist and should influence the demography of one-male units.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00167957
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Cycle synchrony and probability of conception in female hamadryas baboons Papio hamadryas (1994)
    Springer
    Behavioral ecology and sociobiology 35 (1994), S. 175-183 
    Details
    ISSN: 1432-0762
    Keywords: Key words Papio hamadryas ; One-male units ; Probability of conception ; Synchrony of estrus ; Female-female competition
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We investigated the factors affecting conception in a captive population of Papio hamadryas. We collected data on reproductive states from 16 females over 12 years. Probability of conception was related to the outcome of the immediately preceding pregnancy and the fate of the preceding offspring. After abortions or when an infant survived more than 6 months, a female needed more cycles to conceive than when an infant died within the first 6 months post partum. The degree of estrus synchrony within, but not between, one-male units influenced the probability of conception. Females experiencing conceptive estrus showed less synchrony than those experiencing nonconceptive estrus. The number of females simultaneously in estrus within a one-male unit was negatively correlated with the probability of conception. Within our captive population, group size and male and female age had no influence on the probability of conception. The results indicate that sperm may be a limited resource in the one-male reproductive units of hamadryas baboons. Female-female competition for conception may exist and should influence the demography of one-male units.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00167957
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Qualitative and quantitative high performance liquid chromatographic analysis of monoamine neurotransmitters and metabolites in cerebrospinal fluid and brain tissue using reductive electrochemical detection (1990)
    New York, NY : Wiley-Blackwell
    Biomedical Chromatography 4 (1990), S. 215-220 
    Details
    ISSN: 0269-3879
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The application of reductive coulometric electrochemical detection for analysis of the monoamine neurotransmitters norepinephrine, dopamine, and serotonin and their common metabolites in brain and cerebrospinal fluid following separation by isocratic high performance liquid chromatography is described. The high sensitivity and screening capabilities of coulometric electrodes permits the accurate quantitation of as little as 3-5 pg of these compounds in tissue following a simple single step purification procedure. Moreover, comparison of peak height ratios obtained from analysis of authentic reference standards and tissue samples at selected multiple electrode potentials provides a straightforward means for qualitative evaluation of peak identification and purity during analysis of biological samples. The method is comparatively inexpensive and precise within and between day coefficients of variation for most compounds range from 2-5%. Thirty samples can be run in duplicate in a 24 h period.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bmc.1130040509
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Quantitative analysis of disaturated lecithins in human plasma by ammonia chemical ionization mass spectrometry (1981)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 8 (1981), S. 503-505 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three physiologically important disaturated lecithins have been analyzed quantitatively as the acetate derivatives using a solids inlet probe and ammonia chemical ionization. Concentration independent response factors have been determined over a tenfold range that brackets human plasma levels. The results obtained serve as an independent corroboration of gas chromatographic analyses.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200081008
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    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Analysis of mercapturic acid conjugates of xenobiotic compounds using negative ionization and tandem mass spectrometryPresented in part at the 36th Annual Conference on Mass Spectrometry and Allied Topics, San Francisco, 1988. (1993)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 22 (1993), S. 68-76 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectra of mercapturic acid conjugates of two xenobiotic products of lipid peroxidation (trans-4-hydroxy-2-hexenal and trans-4-hydroxy-2-nonenal) as well as conjugates of 1,3-dichloropropene, styrene oxide, 1,2-naphthalene oxide and α-chlorotoluene were obtained using fast atom bombardment or negative chemical ionization. Fragmentation pathways were investigated using linked scan and mass-analyzed ion kinetic energy spectrometric techniques. Characteristics of the spectra obtained using different ionization and sample introduction techniques are compared. Deprotonated molecular ions of mercapturic acids gave simple daughter ion spectra, with the dominant mode of decomposition involving cleavage of C—S bonds giving a characteristic neutral loss of 129 Da Screening for mercapturates in urine samples was performed using neutral loss scanning and yielded limits of detection in the low nanogram per milliliter range. Quantitative analysis of the S-benzyl mercapturic acid at 1 p.p.b. in urine has been demonstrated using combined gas chromatography/electron capture mass spectrometry with d3-S-benzyl mercapturic acid as internal standard.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200220109
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    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Confirmation of oxytetracycline, tetracycline and chlortetracycline residues in milk by particle beam liquid chromatography/mass spectrometryThis work was presented in part at the 38th ASMS Conference on Mass Spectrometry and Allied Topics, Tucson, Arizona, June 1990. (1991)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 20 (1991), S. 789-795 
    Details
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method using particle beam liquid chromatography/mass spectrometry was developed for the confirmation of oxytetracycline, tetracycline and chlortetracycline residues in bovine milk. This method is one of the first to apply particle beam technology to the confirmation of animal drug residues in food products for regulatory purposes. The milk is centrifuged, using molecular weight cut-off filters to remove components of 25 000 daltons and above from the milk. The filtrate is passed through a C-18 sample preparation cartridge which retains the tetracyclines. After the columns are washed with water, the tetracyclines are eluted with 0.1 M oxalic acid in methanol and concentrated. The compounds are separated on a Novapak C-18 column with a methanol-oxalic acid-acetonitrile mobile phase. Negative chemical ionization with selective ion monitoring is used to identify the tetracyclines. The procedure was used to confirm the presence of each tetracycline at 100 ng ml-1 in fortified and incurred milk samples.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200201208
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    Paper (German National Licenses)
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  • 7
    Electronic Resource
    Electronic Resource
    Metabolism of 1,1,1,2,2-pentafluorohexane and 1,1-difluorocyclohexane by rat liver microsomes in vitro (1984)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1984), S. 512-521 
    Details
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metabolism of 1,1,1,2,2-pentafluorohexane with liver microsomes from phenobarbital-treated rats gave only one metabolite, namely, the 5-hydroxy derivative. Under similar conditions 1,1-difluorocyclohexane was metabolized to give mainly the 3- and 4-hydroxy derivatives in the ratio 1:∼5.5 The structures of these metabolites were established by chemical ionization (CI) and/or electron impact (EI) mass spectrometry and confirmed by synthesis in the case of 1,1-difluorocyclohexan-4-ol. Oxidation of 1,1-difluorocyclohexane with lead tetrakis(trifluoroacetate) also gave, inter alia, the 3- and 4-hydroxy derivatives. In saturated hydrocarbons complete replacement of hydrogen by fluorine at one particular carbon will not only block microsomal hydroxylation thereat but will also inhibit hydroxylation at neighbouring hydrogen-bearing carbons, (α almost completely, β markedly, γ slightly).
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200111005
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    Paper (German National Licenses)
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