(Table 2) Relative abundance of planktonic foraminifera species in Pliocene - Early Quaternary sediments from ODP Hole 111-677A

Planktonic foraminifera from Pliocene - Early Quaternary sediments of ODP Hole 111-677A were studied in detail. It was shown that the majority of detected zonal taxa are reliable biostratigraphic reference points. Between 30 and 210 m in the core zones of planktonic foraminifera from PL1b to Pt1 (according to the W.A. Berggren scale) were distinguished. Changes of planktonic foraminifera complexes from sediments of Hole 111-677A are closely associated with climate-controlled development of surface water masses of the Eastern Equatorial Pacific during 4.6-0.65 million years ago. Sharp decrease in equatorial-tropical species about 3.4 million years ago correlated with cessation of surface water exchange between tropical regions of the Pacific and Atlantic oceans due to formation of the Central American isthmus. The paleotemperature method of M.S Barash was used for reconstructing surface temperatures. Maximum temperatures were reconstructed in late Early Pliocene (26.4°C) and in Late Pliocene (26.6°C) and minimum ones - in the beginning of Early Pliocene (18.4°C), in the middle of Late Pliocene (19.6°C). Cold events occurred: 4.6-4.3, 2.8-2.5, and 1.7-1.2 million years ago, and warm: 4.3, 4.18-3.4, 2.5-2.3, and 1 million years ago. In general, the middle of Early Pliocene, the middle of late Pliocene and early Pleistocene are characterized by cold-water conditions, and the end of Early and the end of Late Pliocene - by warm-water conditions.

Metallization of cyanide-modified Pt(111) electrodes with copper

Date of Acceptance: 12/07/2015 The support of the University of Aberdeen is gratefully acknowledged. CW acknowledges a summer studentship from the Carnegie Trust for the Universities of Scotland.

Metallization of cyanide-modified Pt(111) electrodes with copper

Date of Acceptance: 12/07/2015 The support of the University of Aberdeen is gratefully acknowledged. CW acknowledges a summer studentship from the Carnegie Trust for the Universities of Scotland.

In-situ examination of the selective etching of an alkanethiol monolayer covered Au{111} surface

An examination of the selective etching mechanism of a 1-alkanethiol self-assembled monolayer (SAM) covered Au{111} surface using in-situ atomic force microscopy (AFM) and molecular resolution scanning tunnelling microscopy (STM) is presented. The monolayer self-assembles on a smooth Au{111} surface and typically contains nanoscale non-uniformities such as pinholes, domain boundaries and monatomic depressions. During etching in a ferri/ferrocyanide water-based etchant, selective and preferential etching occurs at SAM covered Au(111) terrace and step edges where a lower SAM packing density is observed, resulting in triangular islands being relieved. The triangular islands are commensurate with the Au(111) lattice with their long edges parallel to its [11-0] direction. Thus, SAM etching is selective and preferential attack is localized to defects and step edges at sites of high molecular density contrast.

Mechanism that dictates pore width and <111>a pore propagation in InP

We report a mechanism for pore growth and propagation based on a three-step charge transfer model. The study is supported by electron microscopy analysis of highly doped n-InP samples anodised in aqueous KOH. The model and experimental data are used to explain propagation of pores of characteristic diameter preferentially along the <111>A directions. We also show evidence for deviation of pore growth from the <111>A directions and explain why such deviations should occur. The model is self-consistent and predicts how carrier concentration affects the internal dimensions of the porous structures.

Dissociative adsorption of methane on the Cu and Zn doped (111) surface of CeO2

The development of economical heterogeneous catalysts for the activation of methane is a major challenge for the chemical industry. Screening potential candidates becomes more feasible using rational catalyst design to understand the activity of potential catalysts for CH4 activation. The focus of the present paper is the use of density functional theory to examine and elucidate the properties of doped CeO2. We dope with Cu and Zn transition metals having variable oxidation state (Cu), and a single oxidation state (Zn), and study the activation of methane. Zn is a divalent dopant and Cu can have a +1 or +2 oxidation state. Both Cu and Zn dopants have an oxidation state of +2 after incorporation into the CeO2 (111) surface; however a Hubbard +U correction (+U = 7) on the Cu 3d states is required to maintain this oxidation state when the surface interacts with adsorbed species. Dissociation of methane is found to occur locally at the dopant cations, and is thermodynamically and kinetically more favorable on Zn-doped CeO2 than Cu-doped CeO2. The origins of this lie with the Zn(II) dopant moving towards a square pyramidal geometry in the sub surface layer which facilitates the formation of two-coordinated surface oxygen atoms, that are more beneficial for methane activation on a reducible oxide surface. These findings can aid in rational experimental catalyst design for further exploration in methane activation processes.