A new formula for the total longshore sediment transport rate     

Atilla Bayram  Magnus Larson  Hans Hanson 《Coastal Engineering》2007

A new predictive formula for the total longshore sediment transport (LST) rate was developed from principles of sediment transport physics assuming that breaking waves mobilize the sediment, which is subsequently moved by a mean current. Six high-quality data sets on hydrodynamics and sediment transport collected during both field and laboratory conditions were employed to evaluate the predictive capability of the new formula. The main parameter of the formula (a transport coefficient), which represents the efficiency of the waves in keeping sand grains in suspension, was expressed through a Dean number based on dimensional analysis. The new formula yields predictions that lie within a factor of 0.5 to 2 of the measured values for 62% of the data points, which is higher than other commonly employed formulas for the LST rate such as the CERC equation or the formulas developed by Inman–Bagnold and Kamphuis, respectively. The new formula is well suited for practical applications in coastal areas, as well as for numerical modeling of sediment transport and shoreline change in the nearshore.  相似文献   

Consistent fractionation of 13C in nature and in the laboratory: growth-rate effects in some haptophyte algae     

Bidigare RR  Fluegge A  Freeman KH  Hanson KL  Hayes JM  Hollander D  Jasper JP  King LL  Laws EA  Milder J  Millero FJ  Pancost R  Popp BN  Steinberg PA  Wakeham SG 《Global biogeochemical cycles》1997,11(2):279-292

The carbon isotopic fractionation accompanying formation of biomass by alkenone-producing algae in natural marine environments varies systematically with the concentration of dissolved phosphate. Specifically, if the fractionation is expressed by epsilon p approximately delta e - delta p, where delta e and delta p are the delta 13C values for dissolved CO2 and for algal biomass (determined by isotopic analysis of C37 alkadienones), respectively, and if Ce is the concentration of dissolved CO2, micromole kg-1, then b = 38 + 160*[PO4], where [PO4] is the concentration of dissolved phosphate, microM, and b = (25 - epsilon p)Ce. The correlation found between b and [PO4] is due to effects linking nutrient levels to growth rates and cellular carbon budgets for alkenone-containing algae, most likely by trace-metal limitations on algal growth. The relationship reported here is characteristic of 39 samples (r2 = 0.95) from the Santa Monica Basin (six different times during the annual cycle), the equatorial Pacific (boreal spring and fall cruises as well as during an iron-enrichment experiment), and the Peru upwelling zone. Points representative of samples from the Sargasso Sea ([PO4] < or = 0.1 microM) fall above the b = f[PO4] line. Analysis of correlations expected between mu (growth rate), epsilon p, and Ce shows that, for our entire data set, most variations in epsilon p result from variations in mu rather than Ce. Accordingly, before concentrations of dissolved CO2 can be estimated from isotopic fractionations, some means of accounting for variations in growth rate must be found, perhaps by drawing on relationships between [PO4] and Cd/Ca ratios in shells of planktonic foraminifera.  相似文献   

Pb and Nd isotope constraints on the origin of high Mg and tholeiitic amphibolites,Kolar Schist Belt,South India   总被引：1，自引：0，他引：1  

S. Balakrishnan  G. N. Hanson  V. Rajamani 《Contributions to Mineralogy and Petrology》1991,107(3):279-292

The late Archean, north-south trending Kolar Schist Belt in south India, 4 km wide by 80 km long, is thought to be a suture between two gneiss terranes (Krogstad et al. 1989). Within this volcanics-dominated belt are recognized both tholeiitic and high Mg (komatiitic and picritic) amphibolites, which make up some 70% and 5% respectively of the exposed outcrops. A massive tholeiitic amphibolite separates the belt into western and eastern parts. A Pb-Pb whole-rock age of 2732±155 Ma on samples from a single outcrop of massive tholeiite is a minimum age for this rock. Samples of this rock have _Nd values at 2700 Ma that range between +3.8 and +6.8, ₁ (initial ²³⁸U/²⁰⁴Pb) of 7.5 and K ₁ (initial ²³²Th/²³⁸U) of about 4. Two different types of high-Mg amphibolites are recognized from the western part of the belt: a picritic or P-type, and a komatiitic or K-type. The P-type have highly variable Ce/Al ratios all greater than chondritic, Nd/Yb ratios greater than chondritic, _Nd at 2700 Ma of +1.5 to +8, and Pb isotope compositions variable in ²⁰⁷Pb/²⁰⁴Pb with ₁ of about 8.0 and k ₁ of about 4. The trace-element data suggest that the light-REE enrichment is a character of the mantle source and is not due to residual garnet. The K-type amphibolites have near chondritic Ce/Al and Nd/Yb ratios, _Nd at 2700 Ma of +1.5 to +8, and ₁ of about 8 and k ₁ of about 4. Although the P-type is light-REE enriched compared to the K-type, both types have similar Ce/Nd ratios as well as initial Pb and Nd isotopes. If the 2696±136 Ma age for the Sm-Nd isochron which includes both types of high-Mg amphibolite has any significance it dates the time of light-REE enrichment of the mantle source for the P-type komatiitic amphibolites. The high-Mg amphibolites in the eastern part of the belt are light-REE enriched, have Pb isotopic compositions that are variable in ²⁰⁷Pb/²⁰⁴Pb with a ₁ about 8.5 and _Nd at 2700 Ma of +1.8 to +4.5. Hydrothermal fluids associated with metamorphism and shearing prior to about 2400 Ma ago were responsible for the introduction of gold-quartz-carbonate veins into the Kolar Schist Belt. The Pb isotope composition of galena in these veins suggests that these fluids may have also introduced extraneous Pb from adjacent older granitoid gneisses into the amphibolites, which could be responsible for the variability in the ²⁰⁷Pb/²⁰⁴Pb ratios of the samples. This extraneous Pb probably is not responsible for the distinct Pb isotope character of each type of amphibolite.  相似文献   

Determining the extent of weathering of spilled fuel in contaminated soil using the diastereomers of pristane and phytane     

Cameron P. McIntyre  Paul McA. Harvey  Susan Ferguson  Anna M. Wressnig  Ian Snape  Simon C. George 《Organic Geochemistry》2007,38(12):2131-2134

A method is described for determining the relative extent of weathering in moderately biodegraded, hydrocarbon-contaminated soils from Antarctica. Plotting the pristane diastereomer ratio (PrDR) vs. pristane/phytane (Pr/Ph) allows the relative extent of weathering (primarily evaporation in this case) to be determined. PrDR is used to account for biodegradation as it is independent of evaporation. The method is straightforward and as robust as conventional ratios.  相似文献   

The politics of firm networks: How large firm power limits small firm innovation     

Susan Christopherson  Jennifer Clark 《Geoforum》2007,38(1):1-3

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Species diversity of the Okavango Delta, Botswana   总被引：4，自引：0，他引：4  

Lars Ramberg  Peter Hancock  Markus Lindholm  Thoralf Meyer  Susan Ringrose  Jan Sliva  Jo Van As  Cornelis Vander Post 《Aquatic Sciences - Research Across Boundaries》2006,68(3):310-337

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Simulation of a Ground Water Recirculation Well with a Dual-Column Laboratory Setup     

Suzanne Lesage  Susan Brown  Kelly Millar  Helena Steer 《Ground Water Monitoring & Remediation》2003,23(2):102-110

This paper describes a dual-column laboratory setup consisting of a glass column and a stainless-steel column filled with aquifer material. The setup was used to replicate a ground water recirculation well that serves as an in situ reactor and a combined injection/withdrawal well. The treatment solution consisted of a buffered titanium (III) citrate/vitamin B₁₂ mixture. The first column, representing the well, was made of glass, allowing for visual inspection of the mixing. The stainless-steel column was instrumented with redox (Eh) probes to monitor the changes in redox conditions. The redox measurement showed that, although the sand contained large quantities of iron oxides, the oxidation rate was relatively slow and the titanium solution would remain reduced for some time in the aquifer, continuing to react with the contaminants. This laboratory setup was used to optimize the reagent concentrations and rate of delivery for field implementation. It was found that 4 mM titanium citrate and 3 mg/L vitamin B₁₂ were sufficient to degrade 1,1,2,2-tetrachloroethane and carbon tetrachloride within one day, but not trichloroethylene, which required five days with 10 mM titanium citrate and 5 mg/L vitamin B₁₂.  相似文献   

Mentoring Early Career Faculty in Geography: Issues and Strategies*     

Susan W. Hardwick 《The Professional geographer》2005,57(1):21-27

Early career geography faculty in colleges and universities in the United States are positioned at the leading edge of a challenging period of change in higher education. Demands brought on by new technologies, new administrative and research pressures, and an increasingly competitive campus climate, may make it difficult to balance teaching, research, and service while also trying to maintain a personal life. This article argues that many geographers could benefit from the support of mentoring. Using ideas generated by participants in the Association of American Geographers' recent project, the Geography Faculty Development Alliance, I provide both pragmatic and personal suggestions for establishing these all‐important mentoring relationships to help cope with the pressures facing early career faculty.  相似文献   

Stable carbon isotopic evidence for differences in the dietary origin of bone cholesterol, collagen and apatite: implications for their use in palaeodietary reconstruction     

Susan Jim  Richard P. Evershed 《Geochimica et cosmochimica acta》2004,68(1):61-72

Rats were raised on a variety of isotopically controlled diets comprising 20% C₃, C₄ or marine protein and C₃ and/or C₄ non-protein or energy (i.e. sucrose, starch and oil) macronutrients. Compound specific stable carbon isotope (δ¹³C) analysis was performed on the cholesterol isolated from the diet (n=7 ) and bone (n=15 ) of these animals and the values compared with bulk δ¹³C measurements of bone collagen and apatite. The dietary signals reflected by these three bone biochemical components were investigated using linear regression analysis. δ¹³C values of bone cholesterol were shown to reflect whole diet δ¹³C values, collagen to reflect mainly dietary protein values and apatite to reflect whole diet values. Further correlations between dietary protein-to-energy spacings (Δ¹³C_prot-engy = δ¹³C_protein - δ¹³C_energy) and whole diet-to-bone component fractionations (Δ¹³C_bcomp-wdiet = δ¹³C_{bone component} - δ¹³C_{whole diet}) indicates that for hypothetical diets where protein δ¹³C values are equal to energy values, fractionations between whole diet and bone biochemical fractions are -3.3‰ for cholesterol, +5.4‰ for collagen and +9.5‰ for apatite. Moreover, the narrow range of variation observed in apatite-to-cholesterol spacings (Δ¹³C_apat-bchol) suggests that cholesterol δ¹³C values can potentially also be used as an independent test for the isotopic integrity of apatite δ¹³C values. These insights into bone cholesterol, collagen and apatite dietary signals, diet-to-bone fractionations and bone component-to-bone component spacings provide the basis for more accurate interpretations of the dietary behaviour of archaeological populations and food webs when the δ¹³C analysis of bone is employed.  相似文献   

Fe isotopic fractionation during mineral dissolution with and without bacteria     

Susan L. Brantley  Laura J. Liermann  Ariel Anbar  Jane Barling 《Geochimica et cosmochimica acta》2004,68(15):3189-3204

Fe released into solution is isotopically lighter (enriched in the lighter isotope) than hornblende starting material when dissolution occurs in the presence of the siderophore desferrioxamine mesylate (DFAM). In contrast, Fe released from goethite dissolving in the presence of DFAM is isotopically unchanged. Furthermore, Δ⁵⁶Fe_{solution-hornblende} for Fe released to solution in the presence of ligands varies with the affinity of the ligand for Fe. The extent of isotopic fractionation of Fe released from hornblende also increases when experiments are agitated continuously. The Fe isotope fractionation observed during hornblende dissolution with organic ligands is attributed predominantly to retention of ⁵⁶Fe in an altered surface layer, while the lack of isotopic fractionation during goethite dissolution in DFAM is consistent with the lack of an altered layer. When a siderophore-producing soil bacterium is added to the system (without added organic ligands), Fe released to solution from both hornblende and goethite differs isotopically from Fe in the bulk mineral: Δ⁵⁶Fe_{solution-starting material} = −0.56 ± 0.19 (hornblende) and −1.44 ± 0.16 (goethite). Increased isotopic fractionation is attributed in this case to the fact that as bacterial respiration depletes the system in oxygen and aqueous Fe is reduced, equilibration between aqueous ferrous and ferric iron creates a pool of isotopically heavy ferric iron that is assimilated by bacterial cells. Adsorption of isotopically heavy ferrous iron (Fe(II) enriched in the heavier isotope) or precipitation of isotopically heavy Fe minerals may also contribute to observed fractionations.To test whether these Fe isotope signatures are recorded in natural systems, we also investigated extractions of samples of soils from which the bacteria were isolated. These extractions show variability in the isotopic signatures of exchangeable Fe and Fe oxyhydroxide fractions from one soil sample to another, but exchangeable Fe is observed to be lighter than Fe in soil Fe oxyhydroxides and hornblende. This observation is consistent with isotopically light Fe-organic complexes in soil pore water derived from the Fe-silicate starting materials in the presence of growing microorganisms, as documented in experiments reported here. The contributions from phenomena including organic ligand-promoted nonstoichiometric dissolution of Fe silicates, uptake of ferric iron by organisms, adsorption of isotopically heavy ferrous iron, and precipitation of iron minerals should create complex isotopic signatures in soils. Better understanding of these processes and the timescales over which they contribute to fractionation is needed.  相似文献