Calculating the global contribution of coralline algae to carbon burial

The ongoing increase in anthropogenic carbon dioxide (CO2) emissions is changing the global marine environment and is causing warming and acidification of the oceans. Reduction of CO2 to a sustainable level is required to avoid further marine change. Many studies investigate the potential of marine carbon sinks (e.g. seagrass) to mitigate anthropogenic emissions, however, information on storage by coralline algae and the beds they create is scant. Calcifying photosynthetic organisms, including coralline algae, can act as a CO2 sink via photosynthesis and CaCO3 dissolution and act as a CO2 source during respiration and CaCO3 production on short-term time scales. Long-term carbon storage potential might come from the accumulation of coralline algae deposits over geological time scales. Here, the carbon storage potential of coralline algae is assessed using meta-analysis of their global organic and inorganic carbon production and the processes involved in this metabolism. Organic and inorganic production were estimated at 330 g C m−2 yr−1 and 880 g CaCO3 m−2 yr−1 respectively giving global organic/inorganic C production of 0.7/1.8 × 109 t C yr−1. Calcium carbonate production by free-living/crustose coralline algae (CCA) corresponded to a sediment accretion of 70/450 mm kyr−1. Using this potential carbon storage by coralline algae, the global production of free-living algae/CCA was 0.4/1.2 × 109 t C yr−1 suggesting a total potential carbon sink of 1.6 × 109 t C yr−1. Coralline algae therefore have production rates similar to mangroves, saltmarshes and seagrasses representing an as yet unquantified but significant carbon store, however, further empirical investigations are needed to determine the dynamics and stability of that store

A consistent treatment of link and writhe for open rods, and their relation to end rotation

We combine and extend the work of Alexander & Antman \cite{alexander.82} and Fuller \cite{fuller.71,fuller.78} to give a framework within which precise definitions can be given of topological and geometrical quantities characterising the contortion of open rods undergoing large deformations under end loading. We use these definitions to examine the extension of known results for closed rods to open rods. In particular, we formulate the analogue of the celebrated formula $Lk=Tw+Wr$ (link equals twist plus writhe) for open rods and propose an end rotation, through which the applied end moment does work, in the form of an integral over the length of the rod. The results serve to promote the variational analysis of boundary-value problems for rods undergoing large deformations.Comment: 17 pages, 4 figure

Geocoding library for Microsoft Excel

The task of developing the tool that allows an analyst who is analyzing the real estate market to use online geocoding services is considered. It is assumed that the analyst uses Microsoft Excel and geocoding service offered by Yandex, the most popular data analysis tool and the most popular Russian Internet company

Stroop dilution but not word-processing dilution : evidence for attention capture

Stroop dilution refers to the observation that the impact of a color word on the naming of a color bar is reduced if another word-like object is displayed simultaneously. Recently, Brown, Roos-Gilbert, and Carr (1995) concluded that Stroop dilution is due to early-visual interference. This conclusion was evaluated in three experiments. Experiment 1 showed that, contrary to the predictions of an early-visual interference account, (a) diluters that are similar in terms of visual complexity induced different amounts of dilution and (b) the size of the dilution effect is proportional to the size of the Stroop interference effect when the diluters are used as single distractors. Experiments 2 and 3 revealed that when the position of the color bar is pre-cued, Stroop dilution disappears. We argue that these findings support Van der Heijden’s (1992) attention-capture account of Stroop dilution.The first author was supported by a grant of the Westfalisch-Lippische Universitatsgesellschaft, Biefeld, Germany.peer-reviewe

Integrability of a conducting elastic rod in a magnetic field

We consider the equilibrium equations for a conducting elastic rod placed in a uniform magnetic field, motivated by the problem of electrodynamic space tethers. When expressed in body coordinates the equations are found to sit in a hierarchy of non-canonical Hamiltonian systems involving an increasing number of vector fields. These systems, which include the classical Euler and Kirchhoff rods, are shown to be completely integrable in the case of a transversely isotropic rod; they are in fact generated by a Lax pair. For the magnetic rod this gives a physical interpretation to a previously proposed abstract nine-dimensional integrable system. We use the conserved quantities to reduce the equations to a four-dimensional canonical Hamiltonian system, allowing the geometry of the phase space to be investigated through Poincar\'e sections. In the special case where the force in the rod is aligned with the magnetic field the system turns out to be superintegrable, meaning that the phase space breaks down completely into periodic orbits, corresponding to straight twisted rods.Comment: 19 pages, 1 figur

Solubility determination from clear points upon solvent addition

A method is described for determining the solubility of multicomponent crystalline compounds from clear points upon sample dilution at a constant temperature. Clear points are established by continuously adding a solvent mixture to a suspension of known composition until a clear solution appears. For validation, this solvent addition method is compared to the traditional equilibrium concentration method at constant temperature and the more recent temperature variation method with which clear point temperatures are determined upon increasing the sample temperature. Solubility data of binary systems (1 solute, 1 solvent) measured using the solvent addition method are obtained relatively quickly compared to the equilibrium concentration method. These solubility data are consistent with those of the temperature variation and the equilibrium concentration method. For the temperature variation method, the results are dependent on the heating rate. Likewise, for the solvent addition method, they are dependent on the addition rate. Additionally, for ternary systems involving antisolvent or cocrystals, solubilities are determined at a constant temperature using the solvent addition method. The use of the solvent addition method is especially valuable in the case of solvent mixtures and other complex multicomponent systems, in which the temperature variation method cannot be applied easily