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  • 2000-2004  (155)
  • 1960-1964  (15)
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    Publication Date: 2023-03-08
    Keywords: #22,9/87; #23,5/85; #23,7/85; #23,8/84; #23,9/87; #24,9/87; 1/77peeper,1/77core; 10/24/77; 10/82; 10/83; 10/85; 10/90; 100M; 11/10/78; 11/17/77; 11TW1; 12/83; 12GC2; 14GC1; 16AS; 16S; 2/17/78; 2/25/77; 21F; 24SC1,2; 3/24/78; 3/25/77; 3/85; 3/90A; 3/90B; 3/91A; 3/91B; 36S; 4/90A; 4/90B; 4/90C; 4/91A; 4/91B; 4/91C; 5/16/77; 5/16/78; 5/90; 5/91; 51F; 56M; 6/27/78; 6/30/77; 6/84; 6/90A; 6/90B; 6/90C; 6/91; 62M; 67F; 7/11/77; 7/90; 747-A; 75S; 7BC13; 7BC20; 7GC18; 8/11/78; 8/13/77; 8/84; 8/90A; 8/90B; 812-S; 834-C; 858-C; 8BC23; 8S; 9/27/77; 9/90A; 9/90B; 97S; 9BC26; 9BC27; 9BC33; BC; BC100; BC11; BC114; BC118; BC12; BC14; BC19; BC21; BC24; BC54; BC61; BC68; BC78; BC8; BC82; BCR; Box corer; Box corer (Reineck); BR3.77; CastroCove; Colman1999_001; Colman1999_002; Colman1999_003; Colman1999_004; Colman1999_005; Colman1999_006; Colman1999_007; Colman1999_008; Colman1999_009; Colman1999_010; Colman1999_011; Colman1999_012; Colman1999_013; Colman1999_014; Colman1999_015; Colman1999_016; Colman1999_017; Colman1999_018; Colman1999_019; Colman1999_020; Colman1999_021; Colman1999_022; Colman1999_023; Colman1999_024; Colman1999_025; Colman1999_026; Colman1999_027; Colman1999_028; Colman1999_029; Colman1999_030; Colman1999_031; Colman1999_032; Colman1999_033; Colman1999_034; Colman1999_035; Colman1999_036; Colman1999_037; Colman1999_038; Colman1999_039; Colman1999_040; Colman1999_041; Colman1999_042; Colman1999_043; Colman1999_044; Colman1999_045; Colman1999_046; Colman1999_047; Colman1999_048; Colman1999_049; Colman1999_050; Colman1999_051; Colman1999_052; Colman1999_053; Colman1999_054; Colman1999_055; Colman1999_056; Colman1999_057; Colman1999_058; Colman1999_059; Colman1999_060; Colman1999_061; Colman1999_062; Colman1999_063; Colman1999_064; Colman1999_065; Colman1999_066; Colman1999_067; Colman1999_068; Colman1999_069; Colman1999_070; Colman1999_071; Colman1999_072; Colman1999_073; Colman1999_074; Colman1999_075; Colman1999_076; Colman1999_077; Colman1999_078; Colman1999_079; Colman1999_080; Colman1999_081; Colman1999_082; Colman1999_083; Colman1999_084; Colman1999_085; Colman1999_086; Colman1999_087; Colman1999_088; Colman1999_089; Colman1999_090; Colman1999_091; Colman1999_092; Colman1999_093; Colman1999_094; Colman1999_095; Colman1999_096; Colman1999_097; Colman1999_098; Colman1999_099; Colman1999_100; Colman1999_101; Colman1999_102; Colman1999_103; Colman1999_104; Colman1999_105; Colman1999_106; Colman1999_107; Colman1999_108; Colman1999_109; Colman1999_110; Colman1999_111; Colman1999_112; Colman1999_113; Colman1999_114; Colman1999_115; Colman1999_116; Colman1999_117; Colman1999_118; Colman1999_119; Colman1999_120; Colman1999_121; Colman1999_122; Colman1999_123; Colman1999_124; Colman1999_125; Colman1999_126; Colman1999_127; Colman1999_128; Colman1999_129; Colman1999_130; Colman1999_131; Colman1999_132; Colman1999_133; Colman1999_134; Colman1999_135; Colman1999_136; Colman1999_137; Colman1999_138; Colman1999_139; Colman1999_140; Colman1999_141; Colman1999_142; Colman1999_143; Colman1999_144; Colman1999_145; Colman1999_146; Colman1999_147; Colman1999_148; Colman1999_149; Colman1999_150; Colman1999_151; Colman1999_152; Colman1999_153; Colman1999_154; Colman1999_155; Colman1999_156; Colman1999_157; Colman1999_158; Colman1999_159; Colman1999_160; Colman1999_161; Colman1999_162; Colman1999_163; Colman1999_164; Colman1999_165; Colman1999_166; Colman1999_167; Colman1999_168; Colman1999_169; Colman1999_170; Colman1999_171; Colman1999_172; Core_A/B; core08.3; core10.3; Core19; core28.4; core29.4; Core32; core36.1; core37.4; core38.2; core44.3; Core9; cores1,2,3,9,24,25; CT10-GC3; CT12-BC5; CT15-GC4; CT18-BC7; CT18-GC5; CT21-BC8; Deep-1; Deep-2; Deep-3; DEPTH, sediment/rock; DHC; DIAL; Dial.__A/B; Dialyzer; Diver-held corer; Fall/Winter; FOAM-1; FOAM-2; FOAM-3; FOAM-4; FOAM-5; FOAM-BC-D6/85; FOAM-GC-D5/85; GC; GC16; GC35; Giant box corer; GKG; Grab; GRAB; Gravity corer; GS32; Hand drill; HDRILL; JN3; JN5; JN6; JN6.75; JN7; Latitude of event; Longitude of event; Manop-B; Manop-H; Manop-M; MUC; MultiCorer; NH0487-BC1; NH0487-BC4; NH0987-BC2; NH1085-BC102; NH1085-BC89; NH1087-BC1; NH14; NWC-1; NWC-2; NWC-3; NWC-4; NWC-5; NWC-6; NWC-GC-D5/85; NWC-GC-K4/85; NWC-GC-K4/86; OaklandHarbor; ORFOIS; Origin and Fate of Biogenic Particle Fluxes in the Ocean; Phosphate, flux; Phosphate, flux, diffusive; Phosphate gradient at sediment-water interface; Phosphate gradient at sediment-water interface, maximum; Phosphate gradient at sediment-water interface. minimum; Reference/source; RN1.75; Sample code/label; SP6.77; SPC; Sphincter corer; Spring/Summer; Sta.1; Sta.10; Sta.11; Sta.11.5; Sta.12; Sta.12.5; Sta.13; Sta.14; Sta.15; Sta.2; Sta.3; Sta.4; Sta.6; Sta.7; Sta.8; Sta.A; Sta.B; Sta10; Sta11;BC-24; Sta13;BC-41; Sta14;BC-47; Sta15; Sta16; Sta17; Sta5;BC-6; Sta5;BC-7; Sta6;BC-9; TC; Trigger corer
    Type: Dataset
    Format: text/tab-separated-values, 1312 data points
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 35 (1963), S. 652-654 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Solid state phenomena Vol. 92 (May 2003), p. 125-128 
    ISSN: 1662-9779
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water 42 (2004), S. 0 
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Effects of aquifer travel time on nitrogen reaction and loading to Popponesset Bay, a eutrophic coastal embayment on western Cape Cod, Massachusetts, are evaluated through hydrologic analysis of flow and transport. Approximately 10% of the total nitrogen load to the embayment is intercepted by fresh water ponds and delivered to the coast by connecting streams. For the nitrogen load not intercepted by ponds, we compare two steady-state methods of analyzing nitrogen loss in the aquifer, one using a constant-loss factor and the other time-dependent loss rates. The constant-loss method, which assumes that all similar land uses have the same per unit area loading rate to surface water regardless of location within the watershed, predicts that 42% of the nonpond watershed nitrogen load originated within the zero to 2 yr time-of-travel zone, which is 40% of the contributing area. The time-of-travel loss method calculates loss rates based on aquifer travel times and denitrification reaction kinetics, evaluated separately for carbon-unlimited and carbon-limited cases. Time-of-travel loss calculations for percent of nonpond load that originated within the area of 〈 2 yr aquifer residence time are 64% when carbon is not limiting, but only 49% when carbon limitation is included, not greatly different from the constant-loss method. A feature of the kinetics used is that carbon (and the denitrified nitrogen) is lost rather quickly in the aquifer travel path, after which carbon limitation stops denitrification altogether. Carbon limitation causes the time-of-travel loss model to approximate the constant-loss model such that in most of the watershed, a nearly constant fraction of the nitrogen input is lost in both models.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 185 (1960), S. 112-112 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Could this singular arrangement sometimes constitute a mechanism whereby the members of a vertically migrating species can keep together even when the most important factor, light from the surface, is brusquely interrupted ? Consider a gregarious species, mainly light-con trolled, which occupies ...
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  • 7
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Since the first report of live mammals produced by nuclear transfer from a cultured differentiated cell population in 1995 (ref. 1), successful development has been obtained in sheep, cattle, mice and goats using a variety of somatic cell types as nuclear donors. The ...
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  • 8
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] It is over a decade since the first demonstration that mouse embryonic stem cells could be used to transfer a predetermined genetic modification to a whole animal. The extension of this technique to other mammalian species, particularly livestock, might bring numerous biomedical benefits, ...
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 23 (2000), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Induction of the carbon concentrating mechanism (CCM) has been investigated during the acclimation of 5% CO2-grown Chlamydomonas reinhardtii 2137 mt + cells to well-defined dissolved inorganic carbon (Ci) limited conditions. The CCM components investigated were active HCO3− transport, active CO2 transport and extracellular carbonic anhydrase (CAext) activity. The CAext activity increased 10-fold within 6 h of acclimation to 0·035% CO2 and there was a further slight increase over the next 18 h. The CAext activity also increased substantially after an 8 h lag period during acclimation to air in darkness. Active CO2 and HCO3− uptake by C. reinhardtii cells were induced within 2 h of acclimation to air, but active CO2 transport was induced prior to active HCO3− transport. Similar results were obtained during acclimation to air in darkness. The critical Ci concentrations effecting the induction of active Ci transport and CAext activity were determined by allowing cells to acclimate to various inflow CO2 concentrations in the range 0·035–0·84% at constant pH. The total Ci concentration eliciting the induction and repression of active Ci transport was higher during acclimation at pH 7·5 than at pH 5·5, but the external CO2 concentration was the same at both pHs of acclimation. The concentration of external CO2 required for the full induction and repression of Ci transport and CAext activity were 10 and 100 μM, respectively. The induction of CAext and active Ci transport are not correlated temporally, but are regulated by the same critical CO2 concentration in the medium.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Copenhagen : Munksgaard International Publishers
    Physiologia plantarum 111 (2001), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The effects of the carbonic anhydrase (CA) inhibitors acetazolamide (AZ) and dextran-bound sulfonamide (DBS) on HCO3−-dependent O2 evolution in Chlorella saccharophila were evaluated. Addition of 4 μM AZ or 0.4 mg ml−1 DBS to photosynthesizing cells reduced the O2 evolution rate at low dissolved inorganic carbon (DIC) concentration, decreased the size of the intracellular acid-labile carbon pool, and decreased the apparent affinity of the cells for DIC. Measurement of the whole-cell affinity of cells for CO2 and HCO3− in the presence and absence of inhibitors indicated that active HCO3− transport was inhibited by AZ and DBS. The inhibition of HCO3− transport was independent of the inhibition of external and internal CA. These results suggest that the active uptake of HCO3− occurs initially by the interaction of HCO3− and a CA-like transporter.
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