51 research outputs found
Fringe effect of electrical capacitance and resistance tomography sensors
Because of the 'soft-field' nature, all electrical tomography sensors suffer from electric field distortion, i.e. the fringe effect. In electrical resistance tomography (ERT) sensors, small pin electrodes are commonly used. It is well known that the pin electrodes result in severe electric field distortion or the fringe effect, and the sensing region of such an ERT sensor spreads out of the pin electrode plane to a large volume. This is also true for electrical capacitance tomography (ECT) sensors, even though it is less severe because of larger electrodes and grounded end guards used. However, when the length of electrodes in an ECT sensor without guards is reduced to almost the same dimension as those in an ERT sensor, the fringe effect is equally obvious. To investigate the fringe effect of ERT and ECT sensors with and without guards, simulations were carried out with different length of electrodes and the results are compared with the corresponding 2D simulation. It is concluded that ECT and ERT sensors with longer electrodes have less fringe effect. Because grounded end guards are effective in reducing the fringe effect of ECT sensors, we propose to apply grounded guards in ERT sensors and integrate ECT and ERT sensors together. Simulation results reveal that ERT sensors with grounded guards have less fringe effect. While commonly current excitation is used with ERT sensors, we propose voltage excitation instead to apply the grounded guards. The feasibility of this approach has been verified by experiment. Finally, a common structure for reducing the fringe effect is proposed for ECT and ERT sensors for the first time to simplify the sensor structure and reduce the mutual interference in ECT/ERT dual-modality measurements. © 2013 IOP Publishing Ltd
Increased Cell Proliferation and Mucocyte Density in the Sea Anemone Aiptasia pallida Recovering from Bleaching
Recovery of coral after bleaching episodes is a critical period for the health of the reef ecosystem. While events such as symbiont (genus Symbiodinium) shifting/shuffling or tissue apoptosis have been demonstrated to occur following bleaching, little is known concerning tissue recovery or cell proliferation. Here, we studied the sea anemone Aiptasia pallida exposed to a transient elevation of water temperature combined with high illumination (33°C and 1900 μmolphotons.m.s for 30h). Following such treatment bleached anemones showed a significant reduction of their Symbiodinium density. Cell proliferation in the ectodermis and gastrodermis was determined by assessing the densities of cells labeled with a thymidine analogue (EdU). Cell proliferation significantly increased during the first day following stress in both tissue types. This increased cell proliferation returned to pre-stress values after one week. Although cell proliferation was higher in the ectodermis in absence of stress, it was relatively more pronounced in the gastrodermis of stressed anemones. In addition, the ratio of ectodermal mucocytes significantly increased three weeks after induced stress. These results suggest that thermal/photic stress coupled with the loss of the symbionts is able to enhance cell proliferation in both gastrodermis and ectodermis of cnidarians. While new cells formed in the gastrodermis are likely to host new Symbiodinium, the fate of new cells in the ectodermis was only partially revealed. Some new ectodermal cells may, in part, contribute to the increased number of mucocytes which could eventually help strengthen the heterotrophic state until restoration of the symbiosis
Establishment of endosymbiosis: the case of cnidarians and <i>Symbiodinium</i>
The symbiosis between cnidarians and Symbiodinium algae (dinoflagellates) is the keystone responsible for the formation of the huge and important structures that are coral reefs. Today many environmental and/or anthropogenic threats compromise this tight relationship and lead to more frequent events of drastic loss of Symbiodinium pigments and eventually of algae themselves from cnidarians, better known as cnidarian bleaching. While the mechanisms underlying the collapse of the algae–coral symbiosis are progressively getting unraveled, the understanding of the mechanisms involved in the de novo infection of bleached cnidarians by Symbiodinium remains elusive. In this review, we describe the various steps needed to establish a stable symbiotic relationship between Symbiodinium and cnidarians. We review the mechanisms implicated in host–symbiont recognition and in symbiosome formation and persistence, with a special emphasis on the role played by lectins and Rab proteins. A better understanding of these molecular mechanisms may contribute to the development of strategies to promote post-bleaching recovery of corals
Impairment of symbiont photosynthesis increases host cell proliferation in the epidermis of the sea anemone <i>Aiptasia pallida</i>
Corals exposed to environmental stresses need to engage appropriate physiological strategies to survive. Here, we examined tissue modifications following algal dysfunction. Aiptasia pallida was exposed during 1 week to 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU), the herbicide called diuron. DCMU treatment produced a drastic loss in photosynthetic efficiency and a subsequent diminution of algae density over the following days. Cell proliferation evaluated by measuring the number of cells labeled with a thymidine analogue (EdU) revealed a significant increase in EdU+ cells in the epidermis after 1 week of DCMU incubation and in the gastrodermis at 4 weeks. TUNEL histology showed that the extent of cell death was, however, similar in the epidermis of control and treated specimens. In addition, we noticed a significant effect of DCMU treatment on the density of epidermal mucocytes after 1, 2 and 4 weeks. These results show that inhibition of Symbiodinium photosynthesis in the absence of any known direct effect of DCMU on host cells can induce an increase in epidermal host cell proliferation in both the epidermis and the gastrodermis. While new host gastrodermal cells are likely to promote tissue regeneration in order to recruit new algae, the new host epidermal cells may contribute to tissue adaptation following a decrease in energy income. Some of these new epidermal cells, such as mucocytes, may contribute to an eventual increase in the host heterotrophic ability until restoration of algal autotrophic contribution
Flow Pattern Evolution With Time Mixing of Non-Newtonian Fluid in a Stirred Tank Using Particle Image Velocimetry
Détermination du régime hydrodynamique dans une colonne à bulles par tomographie électrique résistive
peer reviewe
A possible new mineral species, "ferrogatehouseite" (Fe,Mn)5(PO4)2(OH)4 from Conţu Pegmatite, Romania.
peer reviewe
A structural, magnetic, and Mossbauer spectral study of several Na-Mn-Fe-bearing alluaudites
The synthesis and the chemical, structural, magnetic, and Mossbauer spectral characterization of three synthetic alluaudites, Na2Mn2Fe(PO4)(3), NaMn Fe-2(PO4)(3) and (Na2MnFeFeIII)-Fe-II(PO4)(3), and a natural sample with the nominal composition of NaMn Fe-2(PO4)(3), collected in the Buranga pegmatite, Rwanda, are reported. All four compounds have the expected alluaudite monoclinic C2/c structure with the general formula [A(2)A(2)'][A(1)A(1)'A(1)(2)'']M(1)M(2)(2)(PO4)(3) in which manganese(II) is on the M(1) site and manganese(II), iron(III) and, in some cases, iron(II) on the M(2) site. The X-ray structure of Na2Mn2Fe(PO4)(3) also indicates a partially disordered distribution of Na-I and Mn-II on the M(1) and A(1) crystallographic sites. All four compounds are paramagnetic above 40 K and antiferromagnetically ordered below. Above 40 K the effective magnetic moments of NaMnFe2(PO4)(3) and Na2MnFeII Fe-III(PO4)(3) are those expected of high-spin manganese(II) and iron(III) with the (6)A(1g) electronic ground state and high-spin iron(II) with the T-5(2g) electronic ground state. In contrast, the effective magnetic moment of Na2Mn2Fe(PO4)(3) is lower than expected as a result of enhanced antiferromagnetic exchange coupling by the manganese(II) on the M(2) site. The Mossbauer spectra of all four compounds have been measured from 4.2 to 295 K and have been found to be magnetically ordered below 40 K for Na2Mn2Fe(PO4)(3) and similar to35 K for the remaining compounds. The Mossbauer spectra of Na2Mn2Fe(PO4)(3) exhibit the two expected iron(III) quadrupole doublets and/or magnetic sextets expected for a random distribution of manganese(II) and iron(III) ions on the M(2) site. Further, the Mossbauer spectra of (Na2MnFeFeIII)-Fe-II(PO4)(3) exhibit the two iron(II) and two iron(III) quadrupole doublets and/or magnetic sextets expected for a random distribution of iron(II) and iron(III) on the M(2) site. Surprisingly, the synthetic and natural samples of NaMnFe2(PO4)(3) have 19 and 10% of iron(II) on the M(2) site; apparently the presence of some iron(II) stabilizes the alluaudite structure through the reduction of iron(III)-iron(III) repulsion. The temperature dependence of the iron(II) quadrupole splitting yields a 440 to 600 cm(-1) low-symmetry component to the octahedral crystal field splitting at the M(2) site. The iron(II) and iron(III) hyperfine fields observed at 4.2 K are consistent with the presence of antiferromagnetic ordering at low temperatures in all four compounds
Mineralogical and textural evolution of the economic manganese mineralisation in western Rhodope massif, N. Greece
High spatial resolution Raman mapping of complex mineral assemblages: Application on phosphate mineral sequences in pegmatites
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