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  • 1
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effect of feeding the flagellate Isochrysis galbana (Parke; clone T-Iso) of modified lipid composition on the growth and lipid composition of juvenile scallops [Placopecten magellanicus (Gmelin)] was investigated in the spring of 1993. I. galbana grown in 85-liter cage culture turbidostats under conditions of nitrogen limitation had a significantly higher total lipid content than when grown under nutrient-replete conditions. This was due mainly to a doubling in the amount of less unsaturated triacylglycerol in the cells. The concentrations of methyl and ethyl ketones were also greater in nitrogen-limited cells. Diets of nitrogen-limited I. galbana and nutrient-replete I. galbana grown in continuous and semi-continuous cultures were compared. Scallop juveniles were batch fed daily, and measurements of ingestion were determined. Samples of juveniles were removed periodically for determination of organic weight. The juveniles did not grow when fed nitrogen-limited or nutrient-replete I. galbana alone; however, when each diet was supplemented with 20% of the diatom Chaetoceros muelleri (Lemm.), there was a significant increase in growth in the juveniles receiving the nitrogen-limited I. galbana compared with juveniles on other diets. In comparison with I. galbana,  C. muelleri provided a rich source of carbohydrates and the essential fatty acid 20:4ω6. This study shows the importance of providing optimal dietary levels of ω3 and ω6 polyunsaturated fatty acids, as well as less unsaturated fatty acids and carbohydrates.
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 382 (1996), S. 534-536 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Nautilus pompilius L. living at depths of 225-300 m were taken in baited traps from the sunken barrier reef south-east of Port Moresby, Papua New Guinea, and transported to the Motupore Island research station where they were acclimated to experimental temperatures (18 °C) which approximate ...
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  • 3
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Biochemistry 65 (1996), S. 609-634 
    ISSN: 0066-4154
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Chemistry and Pharmacology , Biology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0649
    Keywords: 42.55.Px ; 42.62.Fi ; 07.65.Gj
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract We present an optically stabilized lead-salt diode-laser system which is the nucleus of a very-high-resolution instrument for sub-Doppler molecular spectroscopy in the mid-infrared. By application of external optical feedback, we have narrowed the diode-laser linewidth by two orders of magnitude, yielding a spectral width of less than 200 kHz. The diode- laser frequency is stabilized and controlled via the external reflector by variable-frequency offset-locking the diode-laser to a CO laser frequency. This substantial improvement in the spectral properties enabled us to perform a Lamb-dip experiment on a carbonyl sulfide (OCS) absorption line near 1985 cm−1. We were able to detect a saturated dispersion signal at low pressure (5 Pa) with a signal-to-noise ratio of several thousand. The present paper describes the unique features of the optically stabilized tunable diode-laser system and its use as a spectroscopic tool for sub-Doppler applications.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Antonie van Leeuwenhoek 70 (1996), S. 317-330 
    ISSN: 1572-9699
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 28 (1996), S. 475-480 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas-phase reaction products of the OH radical with 2-ethoxyethyl acetate (EEA, CH3C(O)OCH2CH2OCH2CH3) have been investigated. 1,2-Ethanediol acetate formate (EAF, CH3C(O)OCH2CH2OC(O)H) and ethyl formate (EF, HC(O)OCH2CH3) were identified as the two main products. A third product, ethylene glycol diacetate (EGD, CH3C(O)OCH2CH2OC(O)CH3), was also observed. EAF, EF, and EGD formation yields were determined to be 0.37 ± 0.03 and 0.328 ± 0.018 and 0.040 ± 0.005, respectively. Proposed reaction mechanisms are discussed and compared with these data. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 637-644 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relative rate technique has been used to measure the hydroxyl radical (OH) reaction rate constant of ethyl 3-ethoxypropionate (EEP, CH3CH2(SINGLE BOND)O(SINGLE BOND)CH2CH2C(O)O(SINGLE BOND)CH2CH3). EEP reacts with OH with a bimolecular rate constant of (22.9±7.4)×10-12 cm3 molecule-1s-1 at 297±3 K and 1 atmosphere total pressure. In order to more clearly define EEP's atmospheric reaction mechanism, an investigation into the OH+EEP reaction products was also conducted. The OH+EEP reaction products and yields observed were: ethyl glyoxate (EG, 25±1% HC((DOUBLE BOND)O)C((DOUBLE BOND)O)(SINGLE BOND)O(SINGLE BOND)CH2CH3), ethyl (2-formyl) acetate (EFA, 4.86±0.2%, HC((DOUBLE BOND)O)(SINGLE BOND)CH2(SINGLE BOND)C((DOUBLE BOND)O)(SINGLE BOND)O(SINGLE BOND)CH2CH3), ethyl (3-formyloxy) propionate (EFP, 30±1%, HC((DOUBLE BOND)O)(SINGLE BOND)O(SINGLE BOND)CH2CH2(SINGLE BOND)C((DOUBLE BOND)O)(SINGLE BOND)O(SINGLE BOND)CH2CH3), ethyl formate (EF, 37±1%, HC((DOUBLE BOND)O)O(SINGLE BOND)CH2CH3), and acetaldehyde (4.9±0.2%, HC((DOUBLE BOND)O)CH3). Neither the EEP's OH rate constant nor the OH/EEP reaction products have been previously reported. The products' formation pathways are discussed in light of current understanding of oxygenated hydrocarbon atmospheric chemistry. © 1997 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 29 (1997), S. 445-451 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relative rate technique has been used to measure the hydroxyl radical (OH) reaction rate constant of hexamethyldisiloxane (MM, (CH3)3Si-O-Si(CH3)3), octamethyltrisiloxane (MDM, (CH3)3Si-O-Si(CH3)2-O-Si(CH3)3), and decamethyltetrasiloxane (MD2M, (CH3)3Si-O-Si(CH3)2-O-Si(CH3)2-O-Si(Ch3)3). Hexamethyldisiloxane, octamethyltrisiloxane, and decamethyltetrasiloxane react with OH with bimolecular rate constants of 1.32 ± 0.05 × 10-12 cm3molecule-1s-1, 1.83 ± 0.09 × 10-12 cm3 molecule-1s-1, and 2.66 ± 0.13 × 10-12 cm3molecule-1s-1, respectively. Investigation of the OH + siloxane reaction products yielded trimethylsilanol, pentamethyldisiloxanol, heptamethyltetrasiloxanol, hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, and other compounds. Several of these products have not been reported before because these siloxanes and the proposed reaction mechanisms yielding these products are complicated. Some unusual cyclic siloxane products were observed and their formation pathways are discussed in light of current understanding of siloxane atmospheric chemistry. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 445-451, 1997.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 745-752 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relative rate technique has been used to measure the hydroxyl radical (OH) reaction rate constant of +2-butanol (2BU, CH3CH2CH(OH)CH3) and 2-pentanol (2PE, CH3CH2CH2CH(OH)CH3). 2BU and 2PE react with OH yielding bimolecular rate constants of (8.1±2.0)×10-12 cm3molecule-1s-1 and (11.9±3.0)×10-12 cm3molecule-1s-1, respectively, at 297±3 K and 1 atmosphere total pressure. Both 2BU and 2PE OH rate constants reported here are in agreement with previously reported values [1-4]. In order to more clearly define these alcohols' atmospheric reaction mechanisms, an investigation into the OH+alcohol reaction products was also conducted. The OH+2BU reaction products and yields observed were: methyl ethyl ketone (MEK, (60±2)%, CH3CH2C((DOUBLEBOND)O)CH3) and acetaldehyde ((29±4)% HC((DOUBLEBOND)O)CH3). The OH+2PE reaction products and yields observed were: 2-pentanone (2PO, (41±4)%, CH3C((DOUBLEBOND)O)CH2CH2CH3), propionaldehyde ((14±2)% HC((DOUBLEBOND)O)CH2CH3), and acetaldehyde ((40±4)%, HC((DOUBLEBOND)O)CH3). The alcohols' reaction mechanisms are discussed in light of current understanding of oxygenated hydrocarbon atmospheric chemistry. Labeled (18O) 2BU/OH reactions were conducted to investigate 2BU's atmospheric transformation mechanism details. The findings reported here can be related to other structurally similar alcohols and may impact regulatory tools such as ground level ozone-forming potential calculations (incremental reactivity) [5]. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 745-752, 1998
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  • 10
    Publication Date: 1999-08-17
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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