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  • 2000-2004  (155)
  • 1960-1964  (15)
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  • 1
  • 2
    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
    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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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Plant, cell & environment 24 (2001), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Physiological properties of photosynthesis were determined in the marine diatom, Phaeodactylum tricornutum UTEX640, during acclimation from 5% CO2 to air and related to H2CO3 dissociation kinetics and equilibria in artificial seawater. The concentration of dissolved inorganic carbon at half maximum rate of photosynthesis (K0·5[DIC]) value in high CO2-grown cells was 1009 mmol m−3 but was reduced three-fold by the addition of bovine carbonic anhydrase (CA), whereas in air-grown cells K0·5[DIC] was 71 mmol m−3, irrespective of the presence of CA. The maximum rate of photosynthesis (Pmax) values varied between 300 and 500 μmol O2 mg Chl−1 h−1 regardless of growth pCO2. Bicarbonate dehydration kinetics in artificial seawater were re-examined to evaluate the direct HCO3− uptake as a substrate for photosynthesis. The uncatalysed CO2 formation rate in artificial seawater of 31·65°/oo of salinity at pH 8·2 and 25 °C was found to be 0·6 mmol m−3 min−1 at 100 mmol m−3 DIC, which is 53·5 and 7·3 times slower than the rates of photosynthesis exhibited in air- and high CO2-grown cells, respectively. These data indicate that even high CO2-grown cells of P. tricornutum can take up both CO2 and HCO3− as substrates for photosynthesis and HCO3− use improves dramatically when the cells are grown in air. Detailed time courses were obtained of changes in affinity for DIC during the acclimation of high CO2-grown cells to air. The development of high-affinity photosynthesis started after a 2–5 h lag period, followed by a steady increase over the next 15 h. This acclimation time course is the slowest to be described so far. High CO2-grown cells were transferred to controlled DIC conditions, at which the concentrations of each DIC species could be defined, and were allowed to acclimate for more than 36 h. The K0·5[DIC] values in acclimated cells appeared to be correlated only with [CO2(aq)] in the medium but not to HCO3−, CO32−, total [DIC] or the pH of the medium and indicate that the critical signal regulating the affinity of cells for DIC in the marine diatom, P. tricornutum, is [CO2(aq)] in the medium.
    Type of Medium: Electronic Resource
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  • 7
    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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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 22 (2004), S. 381-382 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] To the editor: A paper in the January issue by Andrews and colleagues describes karyotype abnormalities in cultured human embryonic stem (hES) cell lines. Indeed, other reports have emerged describing similar abnormalities in hES cells, many of which were first communicated at the International ...
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  • 9
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] The increasing use of peptides as pharmaceutical agents, especially in the antiviral and anti-infective therapeutic areas, requires cost-effective production on a large scale. Many peptides need carboxy amidation for full activity or prolonged bioavailability. However, this modification is not ...
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  • 10
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Type 1 diabetes (T1D; or insulin-dependent diabetes mellitus, IDDM) is an autoimmune disease with both genetic and environmental components. In addition to the human leukocyte antigen (HLA) complex, the single major genetic contributor of susceptibility, an unknown number of other unidentified ...
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