Cyclotella paleo-ocellata, a new centric diatom (Bacillariophyta) from Lake Kinneret (Israel)

© Czech Phycological Society (2015). Large, subfossil populations of an unknown centric, planktonic diatom were observed in a lake sediment core from Lake Kinneret (Israel), which is here described as Cyclotella paleo–ocellata sp. nov. The new taxon, which belongs to the Cyclotella ocellata species complex, is described and separated from other similar taxa (e.g., Cyclotella ocellata, Cyclotella kuetzingiana, Cyclotella polymorpha, Cyclotella paraocellata) based on a combination of the following morphological characters: valve diameter, number of orbiculi depressi (circular depressions), number of striae/10 μm, stria length, number and position of rimoportulae and the number of central and marginal fultoportulae. Cyclotella paleo–ocellata can be distinguished mainly by two prominent characteristics: (1) the number and the arrangement of the orbiculi depressi (4–8) which increase with the valve diameter and (2) the marginal fultoportulae, situated on each, every second or third costa. Since Cyclotella paleo–ocellata is at present only known from the subfossil bottom sediments of Lake Kinneret, its ecological preferences are inferred simply from the associated diatom flora

Ferocia gen. nov., a new centric diatom genus (Bacillariophyceae) from the sub-Antarctic region

International audienceA new centric diatom genus, Ferocia Van de Vijver and Houk gen. nov. is described based on Melosira setosa Greville. Several samples collected in lava tunnels on Ile Amsterdam, a small isolated, volcanic island in the southern Indian Ocean where the latter taxon dominated the diatom flora, were investigated. The new genus is characterized by having heavily silicified, spherical frustules, connected into long chains by large, complex linking spines. Valves are dome-shaped with a high mantle with rounded to irregularly shaped areolae. Numerous small rimoportulae forming a marginal ring are present near the mantle edge. The cingulum is composed of a large number of narrow, open copulae. A second species, Ferocia ninae Van de Vijver and Houk sp. nov., is described from the nearby Crozet archipelago. Besides the typical features of the genus Ferocia, the rimoportulae in F. ninae are almost equidistant, the valves have a relatively low valve height and the spines are relatively small. Both F. ninae and F. setosa were found in shaded lava tunnels with a sparse moss vegetation. The two species are illustrated and discussed based on detailed LM and SEM observations

Influence of Terminal Carboxyl Groups on the Structure and Reactivity of Functionalized m-Carboranethiolate Self-Assembled Monolayers

The structure and function of self-assembled monolayers (SAMs) at the nanoscale are determined by the steric and electronic effects of their building blocks. Carboranethiol molecules form pristine monolayers that provide tunable two-dimensional systems to probe lateral and interfacial interactions. Additional omega-functionality, such as carboxyl groups, can be introduced to change the properties of the exposed surfaces. Here, two geometrically similar isomeric m-carborane analogues of m-mercaptobenzoic acid, 1-COOH-7-SH-1,7-C2B10H10 and racem-1-COOH-9-SH-1,7-C2B10H10, are characterized and their SAMs on Au{111} are examined. The latter isomer belongs to the rare group of chiral cage molecules and becomes, to our knowledge, the first example assembled on Au{111}. Although different in symmetry, molecules of both isomers assemble into similar hexagonal surface patterns. The nearest-neighbor spacing of 8.4 +/- 0.4 angstrom is larger than that of non-carboxylated isomers, consistent with the increased steric demands of the carboxyl groups. Computational modeling reproduced this spacing and suggests a tilt relative to the surface normal. However, tilt domains are not observed experimentally, suggesting the presence of strong lateral interactions. Analyses of the influence of the functional groups through the pseudo-aromatic m-carborane skeleton showed that the thiol group attached to either carbon or boron atoms increases the carboxyl group acidity in solution. In contrast, the acidity of the exposed carboxyl group in the SAMs decreases upon surface attachment; computational analyses suggest that the driving force of this shift is the dielectric of the environment in the monolayer as a result of confined intermolecular interactions, proximity to the Au surface, and partial desolvation