Electrical characterization of gel collected from shark electrosensors.

To investigate the physical mechanism of the electric sense, we present an initial electrical characterization of the glycoprotein gel that fills the electrosensitive organs of marine elasmobranchs (sharks, skates, and rays). We have collected samples of this gel, postmortem, from three shark species, and removed the majority of dissolved salts in one sample via dialysis. Here we present the results of dc conductivity measurements, low-frequency impedance spectroscopy, and electrophoresis. Electrophoresis shows a range of large protein-based molecules fitting the expectations of glycoproteins, but the gels of different species exhibit little similarity. The electrophoresis signature is unaffected by thermal cycling and measurement currents. The dc data were collected at various temperatures, and at various electric and magnetic fields, showing consistency with the properties of seawater. The impedance data collected from a dialyzed sample, however, show large values of static permittivity and a loss peak corresponding to an unusually long relaxation time, about 1 ms. The exact role of the gel is still unknown, but our results suggest its bulk properties are well matched to the sensing mechanism, as the minimum response time of an entire electric organ is on the order of 5 ms.

Electron and mass transport in hybrid redox polyether melts contacted with carbon dioxide.

Films of neat metal salts with covalently attached oligoether side chains ([Co(bpy(CO(2)MePEG-350)(2))(3)](ClO(4))(2); bpy is 2,2'-bipyridine, and MePEG-350 is methyl-terminated oligomeric ethylene oxide with an average molecular weight of 350 Da) undergo marked changes in physical and electrochemical properties upon contact with CO(2). Electrochemical measurements indicate that the physical diffusion coefficient (D(PHYS)) of the Co(II) species, the observed rate constant for Co(II/I) self-exchange (k(EX)), and the physical diffusion coefficient of the perchlorate counterion (D(ClO4)) increase from 2.4 x 10(-11) to 7.0 x 10(-10) cm(2)/s, 6.8 x 10(5) to 4.5 x 10(6) M(-1) s(-1), and 3.4 x 10(-10) to 4.3 x 10(-9) cm(2)/s, respectively, as CO(2) pressure is increased from 0 to 2000 psi at 23 degrees C. A reduction in activation energy accompanies the enhancement of each of these properties over this pressure range. Increasing CO(2) pressure from ambient to 1000 psi causes the films to swell 13%, and free-volume theory explains the enhanced mass transport properties of the films. The origin of increases in electron-transfer kinetics is considered. Plots of log(k(EX)) versus log(D(PHYS)) and log(k(EX)) versus log(D(ClO4)) are both linear. This suggests that electron self-exchange is controlled by factors that also affect log(D(PHYS)) or log(D(ClO4)). One explanation is based on plasticization of the oligoether side-chain motions by CO(2) that affect ether dipole repolarization and Co complex diffusion rates. A second explanation for the changes in k(EX) is based on control of electron transfer by relaxation of counterions neighbor to the Co complexes, which is measured by D(ClO4). Both explanations represent a kind of solvent dynamics control of k(EX).