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Unbound sediment

Transport of mud in Long Island Sound requires, first, resuspension of pellets from the surficial layer on the bottom and then the advection and diffusion of the resuspended material. To describe the transport of suspended sediment quantitatively, the sediment concentration gradient in the vertical direction through the water column and the flux of material into (or out of) the bottom layer of unbound sediment must be known. Both quantities depend on the distribution of velocity fluctuations in the tidal stream and so, even in deep water, are sensitive to weather condi-... [Pg.93]

Mass per unit area of mud bottom Reservoirs of unbound sediment Average amount of unbound sediment 0.29 kg/(m yr)... [Pg.98]

Figure 8 Chemiluminescent (A and B) and bioluminescent (C) detections for immobilized hybridizations of PCR product. Dg, digoxigenin Bt, biotin Ad, avidin. Procedure A [30] Biotin moiety is incorporated into PCR products during the amplification reaction, using one 5 -biotinylated primer. The product is hybridized with a Dg-labeled probe and is immobilized on streptavidin-coated magnetic beads. This capture reaction is carried out for 30 min at 37°C. A permanent magnet is used to sediment the beads during washing to remove unbound DNA. By incubation with the washed beads for 45 min at 37°C, anti-Dg antibody conjugated to HRP enzyme is bound to the Dg-labeled probe, and luminol reaction is performed for CL detection. Procedure B [31] Wells of apolystyrene microtiter plate are activated with l-ethyl-3-(3-dimethylaminopropyl)-carbodiimide, and then coated with a labeled cDNA probe complementary to an internal region of the target DNA. Figure 8 Chemiluminescent (A and B) and bioluminescent (C) detections for immobilized hybridizations of PCR product. Dg, digoxigenin Bt, biotin Ad, avidin. Procedure A [30] Biotin moiety is incorporated into PCR products during the amplification reaction, using one 5 -biotinylated primer. The product is hybridized with a Dg-labeled probe and is immobilized on streptavidin-coated magnetic beads. This capture reaction is carried out for 30 min at 37°C. A permanent magnet is used to sediment the beads during washing to remove unbound DNA. By incubation with the washed beads for 45 min at 37°C, anti-Dg antibody conjugated to HRP enzyme is bound to the Dg-labeled probe, and luminol reaction is performed for CL detection. Procedure B [31] Wells of apolystyrene microtiter plate are activated with l-ethyl-3-(3-dimethylaminopropyl)-carbodiimide, and then coated with a labeled cDNA probe complementary to an internal region of the target DNA.
The expansion of the oxygen minimum zone in the incipient North Atlantic during the Upper Cretaceous enhanced the preservation of sedimentary organic matter. Organic carbon values ranging from 1.7 to 13-7% and the proportions of unbound lipid to total lipid content (>70%) support this premise. A present point of contention is the origin of the organic matter-rich Upper Cretaceous deep-sea sediments. [Pg.91]

With eustatic sea level transgression and flooding of continental lowlands, transport of terrigenous organic matter into the North American basin may have increased. Analyses of Upper Cretaceous sediments from DSDP Site 6O3B, lower continental rise east of Cape Hatteras, indicate that, the organic matter was continentally derived. d C values of -23.5 to 27.1°/oo, C/N ratios of 32 to 72, and lipid class maxima of unbound alkanes (C-. and Cp-), unbound fatty acids (C and C2g) and bound fatty acids (C-g. [Pg.91]

Unbound lipid was extracted by refluxing sediment in methanol/toluene/H O for three hours following sonication ( ). [Pg.92]

Unbound lipids, compounds which are generally more labile than their bound counterparts (J 9), represented the greatest proportion of total lipid In each sediment sample. More than 80 of the total lipid was unbound In the black shales Core 34-1 had the highest... [Pg.95]

Bound aliphatic hydrocarbons comprised 7 of the saponifiable lipid (<1 to 15 ug/g). Unbound/bound ratios of <1 to 67 of this hydrocarbon fraction, with the exception of 603B-29-1, agree with values reported in other studies (, 37). Bound alkane distributions were dominated by C or C-, (Figure 3). Even-carbon predominance of alkanes is an anomaly, but distributions similar to those in the present study have been observed in other North Atlantic deep-sea sediments ( 29). The source of these compounds, however, is unknown. [Pg.97]

Bound and unbound short -ohaln and long-chain fatty acids were generally predominated by the even-carbon compounds. Even-carbon preference, both In the short-chain and long-chain range. Is not unoorammon for fatty acids In ancient sediments. Both the Devonian Antrim shale and the Soudan shale have shown similar even-carbon preferences although the respective n alkane fractions lacked odd-carbon preference. [Pg.102]

Distributions among Bound and Unbound Lipid Fractions of Estuarine Sediments... [Pg.198]

Since a layer of unbound particles is almost always present on the muddy bottom of the Sound, and the formation of the permanent sediment (i.e., the sediment not subject to excitation by water movements) occurs below this layer, it follows that the detailed mechanics and local patterns of mud transport by currents in Long Island Sound have no direct bearing on the sedimentation process. In dealing with sediment formation it suffices to know that mud-size minerals are everywhere supplied faster than they can be incorporated into the permanent bottom sediment. [Pg.93]

The tube is transferred, cap side down, into the adapters, which are placed in the rotor buckets. The tubes are centrifuged at 1000 g for 10 min. During centrifugation the sperm, with chromatin-bound vesicles and other proteins, will sediment through the sucrose solution, while unbound components of the extract will not sediment. [Pg.383]

The unbound components and the 1 M sucrose solution are removed by careful aspiration. The sides of the tube are cleaned with a cotton swab, and the cap is unthreaded. The cover glass, onto which the assembly intermediates have been sedimented, is removed and plunged into fixative and processed for immunofluorescence. The fixation and incubation conditions that are appropriate for the specific antibody being used should be applied to the assembly intermediates on the cover slip. The cover slips can be inverted and mounted onto a microscope slide for observation. [Pg.383]


See other pages where Unbound sediment is mentioned: [Pg.96]    [Pg.102]    [Pg.96]    [Pg.102]    [Pg.150]    [Pg.175]    [Pg.94]    [Pg.97]    [Pg.102]    [Pg.102]    [Pg.470]    [Pg.413]    [Pg.1511]    [Pg.541]    [Pg.278]    [Pg.111]   
See also in sourсe #XX -- [ Pg.98 ]




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