A short survey of the environment at the dumping site for Santa Cruz Harbor dredging and A study of seaward dipping internal structures in marine ripple marks at Whaler's Cove, California. Annual report, Part 4, August 1972

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Are white-beaked dolphins Lagenorhynchus albirostris food specialst? Their diet in the southern North Sea

The white-beaked dolphin Lagenorhynchus albirostris is the most numerous cetacean after the harbour porpoise Phocoena phocoena in the North Sea, including Dutch coastal waters. In this study, the diet of 45 white-beaked dolphins stranded on the Dutch coast between 1968 and 2005 was determined by analysis of stomach contents. Although 25 fish species were identified, the diet was dominated by Gadidae (98.0% by weight, 40.0% in numbers), found in all stomachs. All other prey species combined contributed little to the diet by weight (2.0%W). The two most important prey species were whiting Merlangius merlangus (91.1% frequency of occurrence (FO), 30.5%N, 37.6%W) and cod Gadus morhua (73.3%FO, 7.4%N, 55.9%W). In numbers, gobies were most common (54.6%N), but contributed little to the diet by weight (0.6%W). Three stomachs contained different prey compared to the others: one animal had taken 2250 gobies, accounting for 96.4% of all gobies found; one animal had fed on 29 small sepiolids; and one animal had solely taken haddock Melanogrammus aeglefinus. Squid and haddock were not found in any other stomach. The overall diet showed a lasting predominance of whiting and cod, without clear changes over time (35 years) or differences between sexes or size-classes of dolphins. This study adds to earlier published and unpublished data for Dutch coastal waters and agrees well with studies of white-beaked dolphins from other parts of the species’ range, in the North Sea and in Canadian waters, with Gadidae dominating the diet on both sides of the Atlantic

Microscopic laser-driven high-energy colliders

The concept of a laser-guided $e^+e^-$ collider in the high-energy regime is presented and its feasibility discussed. Ultra-intense laser pulses and strong static magnetic fields are employed to unite in one stage the electron and positron acceleration and their head-on-head collision. We show that the resulting coherent collisions in the GeV regime yield an enormous enhancement of the luminosity with regard to conventional incoherent colliders

Alien Registration- Champagne, C Leopold (Lewiston, Androscoggin County)

https://digitalmaine.com/alien_docs/29384/thumbnail.jp

The Federal Waste Water Treatment System Construction Grant Program: What It Requires of States and How It Works

This paper is the result of a study conducted to inform the author as to how the Environmental Protection Agency (EPA) relates to state and intrastate programs that deal with waste water treatment systems in a coastal state. The investigation centered on how EPA actually manages its functions and assistance directed towards state-level and local-level efforts to control sewage treatment facilities. The study was not limited only to the federal-to-state-flow dynamics. It also looked at areas of purely state function, state-to-local flow, and also the opposite situation of local-to-sate-to-federal oriented inputs

A simple interpretation of the Fe2(-) photoelectron spectrum

The photoelectron spectrum of Fe2(-) can be simply interpreted in terms of electron detachment from the mildly bonding 4s sigma sup * sub u orbital of a (4s sigma sub s)(sup 2) (4s sigma sup * sub u)(sup 2) (3d)(sup 13) anion. This interpretation implies a (4s sigma sub g)(sup 2) (4s sigma sup * sub u)(sup1) (3d)(sup13) configuration for the ground state of Fe2, correlating with one ground state (4s2 3d6) and one excited state (4s1 3d7) Fe atom. A comparison of the bond length and vibrational frequency of Fe2 to values for transition metal dimers containing single 4s-4s bonds is suggestive of 3d-3d bonding in this molecule. The results of preliminary full-valence configuration interaction calculations provide stron support for the proposed Fe2 and Fe2(-) configurations

Enhanced Electrochemistry of Nanoparticle-Embedded Polyelectrolyte Films: Interfacial Electronic Coupling and Distance Dependence

Factors affecting the electronic communication believed to be responsible for the enhanced solution electrochemistry observed at electrodes modified with hybrid polyelectrolyte–nanoparticle (PE–NP) film assemblies were systematically investigated. Specifically, the faradaic current and voltammetric peak splitting recorded for cyclic voltammetry of ferricyanide redox species (Fe(CN)63−/4−) at films constructed with various architectures of citrate-stabilized gold NPs embedded in polyelectrolyte films composed of poly-l-lysine and poly-S-styrene were used to establish the relative importance of both distance and electronic coupling. Layer-by-layer construction of PE–NP films allowed for the position and density of NPs to be varied within the film to assess electronic coupling between particles (interparticle coupling) as well as at the electrode–film interface. The cumulative results observed at these films suggest that, while distance dependence prevails in nearly every case and interparticle coupling can contribute to facilitating the Fe(CN)63−/4− electrochemistry, interfacial electronic coupling of the PE–NP films is of critical importance and decoupling is easily achieved by disengaging NP–electrode interactions

Ultra-fast Formation of Stable Nanoparticle Film Assemblies

Novel assembled films of monolayer-protected clusters (MPCs) can be grown on gold and glass substrates with a 20-fold higher efficiency than established procedures. Thick MPC films grown using this new method, which can easily be scaled up or automated, are extremely stable and have properties identical to traditionally formed nanoparticle films, including unique quantized double layer charging effects. This new procedure for growing nanoparticle films shares the versatility of the traditional method but exhibits accelerated growth attributed to highly efficient sorption and mobility of metal ion linkers within swelled films and improved mass transfer of nanoparticles to assembly sites. Concentration and pH effects on the mechanism of film growth are shown to have substantial impact on the efficiency

Sintering-Induced Nucleation and Growth of Noble Metal Nanoparticles for Plasmonic Resonance Ceramic Color

This study demonstrates the formation of nanoparticles (NPs) from metal salts within ceramic glazes, such that the use of this colorant technology is more accessible to artisans, employs less metal content, is less environmentally harmful, and allows for the use of traditional kilns. Gold NPs have been demonstrated to possess a specific, low material loading use as a ceramic glaze colorant via plasmon resonance. Pre-synthesized gold NPs that are added to ceramic glazes have been found to significantly change in size after firing in both reductive and oxidative atmospheres, but still maintain some size relationships and color properties. Unfortunately, it is not viable for the art community to fabricate and employ gold NP systems with high precision in a studio setting; however, the use of noble metal salts or metal oxides are realistic. To that end, this work investigates spontaneous gold and silver NP synthesis by the firing-induced development of NPs from metallic salts included within the glaze materials. Glaze samples with gold and silver salts are fired in reductive and oxidative environments, yielding a range of surface plasmon coloring effects for ceramic coloring. Additionally, the use of gold NP waste (precipitated Au NPs waste) was added to wet ceramic glazes to investigate firing effects on NPs precipitate and potential use as an alternative colorant. Sintering-induced NP nucleation and growth was observed after firing in both oxidation and reduction environments, although to differing degrees. The direct noble metal salt application process eliminates the need for preliminary gold NP synthesis, thus allowing for more practical and environmentally friendly methods in creating plasmonic resonance ceramic coloring, potentially reflective of the processes employed in ancient nanoparticle glasses