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321.
Riparian vegetation is known to exert a number of mechanical and hydrologic controls on bank stability. In particular, plant roots provide mechanical reinforcement to a soil matrix due to the different responses of soils and roots to stress. Root reinforcement is largely a function of the strength of the roots crossing potential shear planes, and the number and diameter of such roots. However, previous bank stability models have been constrained by limited field data pertaining to the spatial and temporal variability of root networks within stream banks. In this paper, a method is developed to use root‐architecture data to derive parameters required for modeling temporal and spatial changes in root reinforcement. Changes in root numbers over time were assumed to follow a sigmoidal curve, which commonly represents the growth rates of organisms. Regressions for numbers of roots crossing potential shear planes over time showed small variations between species during the juvenile growth phase, but extrapolation led to large variations in root numbers by the time the senescent phase of the sigmoidal growth curve had been reached. In light of potential variability in the field data, the mean number of roots crossing a potential shear plane at each year of tree growth was also calculated using data from all species and an additional sigmoidal regression was run. After 30 years the mean number of roots predicted to cross a 1 m shear plane was 484, compared with species‐specific curves whose values ranged from 240 roots for black willow trees to 890 roots for western cottonwood trees. In addition, the effect of spatial variations in rooting density with depth on stream‐bank stability was modeled using the bank stability and toe erosion model (BSTEM). Three root distributions, all approximating the same average root reinforcement (5 kPa) over the top 1 m of the bank profile, were modeled, but with differing vertical distributions (concentrated near surface, non‐linear decline with depth, uniform over top meter). It was found that stream‐bank FS varied the most when the proportion of the failure plane length to the depth of the rooting zone was greatest. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
322.
323.
Several mechanisms contribute to streambank failure including fluvial toe undercutting, reduced soil shear strength by increased soil pore‐water pressure, and seepage erosion. Recent research has suggested that seepage erosion of noncohesive soil layers undercutting the banks may play an equivalent role in streambank failure to increased soil pore‐water pressure. However, this past research has primarily been limited to laboratory studies of non‐vegetated banks. The objective of this research was to utilize the Bank Stability and Toe Erosion Model (BSTEM) in order to determine the importance of seepage undercutting relative to bank shear strength, bank angle, soil pore‐water pressure, and root reinforcement. The BSTEM simulated two streambanks: Little Topashaw Creek and Goodwin Creek in northern Mississippi. Simulations included three bank angles (70° to 90°), four pore‐water pressure distributions (unsaturated, two partially saturated cases, and fully saturated), six distances of undercutting (0 to 40 cm), and 13 different vegetation conditions (root cohesions from 0·0 to 15·0 kPa). A relative sensitivity analysis suggested that BSTEM was approximately three to four times more sensitive to water table position than root cohesion or depth of seepage undercutting. Seepage undercutting becomes a prominent bank failure mechanism on unsaturated to partially saturated streambanks with root reinforcement, even with undercutting distances as small as 20 cm. Consideration of seepage undercutting is less important under conditions of partially to fully saturated soil pore‐water conditions. The distance at which instability by undercutting became equivalent to instability by increased soil pore‐water pressure decreased as root reinforcement increased, with values typically ranging between 20 and 40 cm at Little Topashaw Creek and between 20 and 55 cm at Goodwin Creek. This research depicts the baseline conditions at which seepage undercutting of vegetated streambanks needs to be considered for bank stability analyses. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
324.
Michael A. Rasheed Kara R. Dew Len J. McKenzie Robert G. Coles Simon P. Kerville Stuart J. Campbell 《Continental Shelf Research》2008
Detailed data on seagrass distribution, abundance, growth rates and community structure information were collected at Orman Reefs in March 2004 to estimate the above-ground productivity and carbon assimilated by seagrass meadows. Seagrass meadows were re-examined in November 2004 for comparison at the seasonal extremes of seagrass abundance. Ten seagrass species were identified in the meadows on Orman Reefs. Extensive seagrass coverage was found in March (18,700 ha) and November (21,600 ha), with seagrass covering the majority of the intertidal reef-top areas and a large proportion of the subtidal areas examined. There were marked differences in seagrass above-ground biomass, distribution and species composition between the two surveys. Major changes between March and November included a substantial decline in biomass for intertidal meadows and an expansion in area of subtidal meadows. Changes were most likely a result of greater tidal exposure of intertidal meadows prior to November leading to desiccation and temperature-related stress. 相似文献
325.
Abstract The main mesoscopic features of the ductile deformation in the Hongusan region of the Ryoke Belt can be explained in terms of a single deformation phase, Dm . The associated stretching lineation is roughly east–west and has an associated top-to-the-west sense of shear. This information fills an important gap in our knowledge about the deformational history of the Ryoke metamorphic belt. Andalusite porphyroblasts are well-developed in the Hongusan area and their microstructure can be used to link the deformational history with the metamorphism. However, the andalusite porphyroblasts show both intertectonic and post-tectonic microstructures. Some porphyroblasts have an intertectonic core and post-tectonic rim. Analysis of associated metamorphic minerals and bulk-rock chemistry suggests that the distinct types of microstructure can be explained in terms of distinct formation reactions related to regional and contact metamorphism. The intertectonic microstructure shows the presence of a deformation pre-dating Dm , referred to as Dc . These two deformation stages are sufficient to account for all the main deformation features. The distribution of post-tectonic andalusite growth shows a very broad thermal effect around an intrusion in the area. This can help place constraints on the thermal history of the Ryoke metamorphic belt. 相似文献
326.
Arumugam Sakunthalai Ramadhas Chandrasekaran Muraleedharan Simon Jayaraj 《洁净——土壤、空气、水》2008,36(12):978-983
Biodiesel is a renewable alternative fuel that can be used as substitute for mineral diesel. The use of biodiesel in diesel engines reduces all of the exhaust emissions expect NOx. The higher temperature in the combustion chamber increases the NOx emissions. The recirculation of a small percentage of cooled exhaust gases into the combustion chamber through the intake manifold reduces the in‐cylinder temperature. Moreover, the cooling of exhaust gases before mixing with fresh air introduced to the engine does not affect its volumetric efficiency but it absorbs the heat of combustion. This leads to a reduction in NOx emissions and improves the engine brake thermal efficiency. This paper describes the investigation of the performance and emission characteristics of a biodiesel‐fueled, naturally aspirated, single cylinder diesel engine with cooled exhaust gas recirculation. 相似文献
327.
There are four extensive sandbanks in the vicinity of the Isle of Portland, a headland in the English Channel. The formation and maintenance of the two most prominent of these sandbanks (one on either side of the headland) can largely be explained by net bedload convergence, driven by instantaneous headland eddies generated by tidal flow past the headland. However, there are also two less prominent sandbanks (again, one on either side of the headland), which are not located in zones of bedload convergence. It is suggested here that these latter two sandbanks were formed when the Isle of Portland was isolated from the mainland by a tidal strait. Relative sea-level data and radiocarbon dates indicate that this would have occurred ca. 9–7 ka BP, prior to the closure of the strait by sedimentation. Tidal flow through this strait generated eddy systems in addition to the headland eddies, leading to the formation of associated headland/island sandbanks. At 7 ka BP, sedimentation resulted in closure of the strait, leading to the present-day headland configuration, and subsequent reworking of these now moribund sandbanks formed by the strait. A series of idealised morphological model experiments, parameterised using bedrock depths and glacial isostatic adjustment model output of relative sea level, are here used to simulate this hypothesised sequence of sandbank evolution over the Holocene. The results of the model experiments are corroborated by in situ observations of bedforms and sediment characteristics, and by acoustic Doppler current profiler (ADCP) data applied to predictions of bedload transport over the sandbanks. In addition to demonstrating the mechanism which leads to the formation of sandbanks by tidal flow through a strait, the model results show that upon subsequent closure of such a strait, these sandbanks will no longer be actively maintained, in contrast to sandbanks which are continuously maintained by headland eddies. 相似文献
328.
Most-probable-number (MPN) dilution series were used to enumerate and isolate bacteria from bulk water, suspended aggregates, the oxic layer, and the oxic–anoxic transition zone of the sediment of a tidal flat ecosystem in the southern North Sea. The heterotrophic aerobic bacteria were able to grow on agar-agar, alginate, cellulose, chitin, dried and ground Fucus vesiculosus, Marine Broth 2216, palmitate, and starch. MPN counts of bulk water and aggregate samples ranged between 0.18?×?101 and 1.1?×?106 cells per milliliter and those of the sediment surface and the transition zone between 0.8?×?101 and 5.1?×?107 cells per gram dry weight. Marine Broth and F. vesiculosus yielded the highest values of all substrates tested and corresponded to 2.3–32% of 4,6-diamidinophenyl indole cell counts. Strains of seven phylogenetic classes were obtained: Actinobacteria, Bacilli, α- and γ-Proteobacteria, Sphingobacteria, Flavobacteria, and Planctomycetacia. Only with agar-agar as substrate could organisms of all seven classes be isolated. 相似文献
329.
Chuan Zhao Thorsten Brinkhoff Malte Burchardt Meinhard Simon Gunther Wittstock 《Ocean Dynamics》2009,59(2):305-315
Adhesion of two marine bacteria Shewanella sp. strain T1 and Pseudoalteromonas sp. strain T8, on differently terminated alkanethiolate self-assembled monolayers on gold was investigated. The selected
model surfaces—terminated by CH3, OH, NH2, COOH, OH-terminated oligo(ethylene glycol), and methyl-terminated oligo(ethylene glycol)—are characterized by contact angle
measurement using water, methylene iodide, 1-bromonaphthalene, and formamide. Surface free energies were calculated. Cell
counting of the two bacterial strains on the model surfaces after different times revealed differences between the two strains
by at least one order of magnitude. For the different surfaces, the bacteria showed comparably small selectivity. Atomic force
microscopy images of adhered bacteria showed very different fingerprints on the different surfaces.
Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible to authorized users. 相似文献
330.
Ineffective Natural Attenuation of Degradable Organic Compounds in a Phenol-Contaminated Aquifer 总被引:4,自引:0,他引:4