Spontaneous Strain Research Articles

Rational Selection of Mixed Yeasts Starters for Agave Must Fermentation

Tequila and mezcal are both traditional Mexican liquors that are produced from cooked Agave spp. must fermentation and usually rely on spontaneous or pure Saccharomyces cerevisiae strain inoculation. In order to contribute to the rational selection of yeast starters for tequila and mezcal productions, we tested a collection of 25 yeasts originally isolated from mezcal musts, spanning 10 different yeast species. These strains were first characterized in a semi synthetic medium (labeled as M2, having 90 g/L fructose and 10 g/L glucose of initial hexoses) at 48 h of culture, observing a differential pattern in the consumption of sugars and productivity. Selected Saccharomyces strains left around 10 g/L of fructose and showed higher fermentation performance. However, some non-Saccharomyces strains, specifically from Torulospora (Td), Kluyveromyces (Km), and Zygosaccharomyces (Zb) genera, consumed almost all the sugar (i.e., Km1Y9 with <5 g/L) and had a high productivity of ethanol. In general, all Saccharomyces strains presented a high production of ethyl-butyrate, ethyl-decanoate, and ethyl-hexanoate with peaks of 10, 38, and 3 μg/L, respectively. In addition, some Kluyveromyces and Torulospora strains showed a high production of phenyl ethyl acetate (i.e., Km1D5 with up to 1400 μg/L); isoamyl acetate (i.e., Km1D5 and Td1AN2 with more than 300 μg/L), and hexyl acetate (i.e., Td1AN2 with 0.3 μg/L). Representative strains of the most productive genera (Saccharomyces, Torulospora, and Kluyveromyces) were selected to evaluate their fermentative performance and survival in a mixed culture on a medium based on Agave tequilana must, and their population kinetics was characterized using specific fluorescent in situ hybridization (FISH) probes in a qualitative and semi-quantitative analysis during fermentation. We observed that the mixture ratios of 0.1:1:1 or 1:1:1 (Saccharomyces:Kluyveromyces:Torulospora), maintained good fermentation productivities, with alcohol yields above 0.45 g/g, and allowed a high survival rate of the non-Saccharomyces strains during the fermentation process. Finally, mixed inoculum fermentations on A. tequilana must medium, including different Saccharomyces strains and the finally selected Torulospora and Kluyveromyces strains, showed the best production parameters in terms of ethanol, carbon dioxide, glycerol, and acetic acid values, as well as improved volatile metabolite profiles as compared to the pure cultures. All these data were used to propose a methodology of selection of strains to be used as a pure or mixed starter for tequila and mezcal fermentations, with high primary metabolite productivity and desired aromatic profile.

Monoclinic–orthorhombic first-order phase transition in K2ZnSi5O12 leucite analogue; transition mechanism and spontaneous strain analysis

AbstractHydrothermally synthesised K2ZnSi5O12 has a polymerised framework structure with the same topology as leucite (KAlSi2O6, tetragonal I41/a), which has two tetrahedrally coordinated Al3+ cations replaced by Zn2+ and Si4+. At 293 K it has a cation-ordered framework P21/c monoclinic structure with lattice parameters a = 13.1773(2) Å, b = 13.6106(2) Å, c = 13.0248(2) Å and β = 91.6981(9)°. This structure is isostructural with K2MgSi5O12, the first cation-ordered leucite analogue characterised. With increasing temperature, the P21/c structure transforms reversibly to cation-ordered framework orthorhombic Pbca. This transition takes place over the temperature range 848−863 K where both phases coexist; there is an ~1.2% increase in unit cell volume between 843 K (P21/c) and 868 K (Pbca), characteristic of a first-order, displacive, ferroelastic phase transition. Spontaneous strain analysis defines the symmetry- and non-symmetry related changes and shows that the mechanism is weakly first order; the two-phase region is consistent with the mechanism being a strain-related martensitic transition.

Unusual stress and strain concentration behaviors at the circular hole of a large monodomain liquid crystal elastomer sheet

Liquid crystal elastomers combine the hyperelasticity of elastomers with the multi-functionality of liquid crystals and have emerged as an important class of soft active materials. Monodomain liquid crystal elastomers under loading exhibit the soft elastic behavior due to the stress induced director rotation and the resulting spontaneous strain. Here, we numerically study their stress and strain concentration behavior by considering the classical example, a large sheet with a small circular hole in the middle under uniaxial loading. The concentration behavior is found to be very different from regular elastomers. Firstly, the concentration factors are much bigger at both small and large strains. Secondly, the locations of the strain concentration may not coincide with that of the stress concentration. Detailed analysis of the director rotation and the resulting spontaneous strain around the free edge of the hole are shown to be the main causes for the unusual concentration behavior. Moreover, under a given strain, the stress level of the LCE sample, and therefore the free energy, is slightly lower than that of the neo-Hookean material, while the local free energy density on the hole edge is much bigger due to the severer concentrations. By considering material parameters obtained from various samples of polysiloxane and polyacrylate side-chain nematic elastomers, we find that their stress and strain concentration behaviors are qualitatively similar but quantitatively quite different. As a result, at a prescribed strain, the samples with a larger maximal spontaneous strain has severer stress and strain concentrations. The stress concentration factor difference scaled by a coupling constant that combines the effect of the two material parameters, r and a, increases as the semi-soft coefficient a decreases. Similar results are found for the scaled maximal spontaneous strains and the scaled strain concentration factor difference at small strains.

Inoculation of grape musts with single strains of Saccharomyces cerevisiae yeast reduces the diversity of chemical profiles of wines.

Anecdotal evidence suggests that spontaneous alcoholic fermentation of grape juice is becoming a more popular option in global wine production. Wines produced from the same grape juice by inoculation or spontaneous fermentation usually present distinct chemical and sensorial profiles. Inoculation has been associated with more similar end-products, a loss of typicity, and lower aroma complexity, and it has been suggested that this may be linked to suppression of the local or regional wine microbial ecosystems responsible for spontaneous fermentations. However, whether inoculated fermentations of different juices from different regions really end up with a narrower, less diverse chemical profile than those of spontaneously fermented juices has never been properly investigated. To address this question, we used grape juice from three different varieties, Grüner Veltliner (white), Zweigelt (red), and Pinot noir (red), originating from different regions in Austria to compare spontaneous and single active dry yeast strains inoculated fermentations of the same grape samples. The chemical analysis covered primary metabolites such as glycerol, ethanol and organic acids, and volatile secondary metabolites, including more than 40 major and minor esters, as well as higher alcohols and volatile fatty acids, allowing an in depth statistical evaluation of differences between fermentation strategies. The fungal (mainly yeast) communities throughout fermentations were monitored using automated ribosomal intergenic spacer analysis. The data provide evidence that inoculation with single active dry yeast strains limits the diversity of the chemical fingerprints. The fungal community profiles clearly show that inoculation had an effect on fermentation dynamics and resulted in chemically less diverse wines.

Trojans That Flip the Black Phase: Impurity-Driven Stabilization and Spontaneous Strain Suppression in γ-CsPbI3 Perovskite

The technological progress and widespread adoption of all-organic CsPbI3 perovskite devices is hampered by its thermodynamic instability at room temperature. Because of its inherent tolerance toward deep trap formation, there has been no shortage to exploring which dopants can improve the phase stability. While the relative size of the dopant is important, an assessment of the literature suggests that its relative size and impact on crystal volume do not always reveal what will beneficially shift the phase transition temperature. In this perspective, we analyze the changes in crystal symmetry of CsPbI3 perovskite as it transforms from a thermodynamically stable high-temperature cubic (α) structure into its distorted low-temperature tetragonal (β) and unstable orthorhombic (γ) perovskite structures. Quantified assessment of the symmetry-adapted strains which are introduced due to changes in temperature and composition show that the stability of γ-CsPbI3 is best rationalized from the point of view of crystal symmetry. In particular, improved thermal-phase stability is directly traced to the suppression of spontaneous strain formation and increased crystal symmetry at room temperature.

Two-dimensional ferroelasticity in van der Waals \u03b2\u2019-In2Se3

Two-dimensional (2D) materials exhibit remarkable mechanical properties, enabling their applications as flexible and stretchable ultrathin devices. As the origin of several extraordinary mechanical behaviors, ferroelasticity has also been predicted theoretically in 2D materials, but so far lacks experimental validation and investigation. Here, we present the experimental demonstration of 2D ferroelasticity in both exfoliated and chemical-vapor-deposited β’-In2Se3 down to few-layer thickness. We identify quantitatively 2D spontaneous strain originating from in-plane antiferroelectric distortion, using both atomic-resolution electron microscopy and in situ X-ray diffraction. The symmetry-equivalent strain orientations give rise to three domain variants separated by 60° and 120° domain walls (DWs). Mechanical switching between these ferroelastic domains is achieved under ≤0.5% external strain, demonstrating the feasibility to tailor the antiferroelectric polar structure as well as DW patterns through mechanical stimuli. The detailed domain switching mechanism through both DW propagation and domain nucleation is unraveled, and the effects of 3D stacking on such 2D ferroelasticity are also discussed. The observed 2D ferroelasticity here should be widely available in 2D materials with anisotropic lattice distortion, including the 1T’ transition metal dichalcogenides with Peierls distortion and 2D ferroelectrics such as the SnTe family, rendering tantalizing potential to tune 2D functionalities through strain or DW engineering.

Antiferroelectricity in pure ferroelastics

In pure ferroelastics, the coupling existing under applied electric field between spontaneous strain and electric polarization is shown theoretically to transform the paraelastic and ferroelastic phases into polarized phases. This effect is rooted in the existence in the zero-field crystal structure of most ferroelastics of polarizable crystallographic sites forming an antiferroelectric array of dipoles. Under high fields the polar ferroelastic phase can become ferroelectric across a first-order isostructural transition, which exhibits a double hysteresis loop.

Structural and Electronic Properties of Ag-Doped in Ba-Site of YBa<sub>2-x</sub>Ag<sub>x</sub>Cu<sub>3</sub>O<sub>δ</sub> Using Density Functional Theory via First Principle Study

This study reports on the First Principle Study via Density Functional Theory (DFT) used to determine the structural and electronic properties of Ag-dopant in Ba-site of YBa2-xAgxCu3Oδ superconductor. The computational method adopting CASTEP computational code was used to calculate the structural and electronic properties for Ag-dopant in range of x=0.150 to x=0.250 in Ba-site of YBa2-xAgxCu3Oδ to enhance the performance finding of experimental work shown at dopant x=0.20 ceramic superconductor. The structural changes in terms of lattice parameters were compared as the percentage of dopant increases to seek both CuO chain and CuO2 plane bond length and the spontaneous strain variance on the structure orthorhombicity. The crystal structure constructed and calculated using Visual Crystal Approximation (VCA) applying the local density approximation (LDA) and ultrasoft pseuodopotential. Geometry optimization shown energy converged at 400 eV with k-point sampling of 4x4x1. The structural properties of YBa2-xAgxCu3Oδ are observed to be approximately close to the experimental data obtained by other researches. The electronic properties were determined via energy band gap, density of states and electron energy differences visualisation a to further enhance the experimental findings.

Effect of mismatch repair on the mutational footprint of the bacterial SOS mutator activity

The bacterial SOS response to DNA damage induces an error-prone repair program that is mutagenic. In Escherichia coli, SOS-induced mutations are caused by the translesion synthesis (TLS) activity of two error-prone polymerases (EPPs), Pol IV and Pol V. The mutational footprint of the EPPs is confounded by both DNA damage and repair, as mutations are targeted to DNA lesions via TLS and corrected by the mismatch repair (MMR) system. To remove these factors and assess untargeted EPP mutations genome-wide, we constructed spontaneous SOS mutator strains deficient in MMR, then analyzed their mutational footprints by mutation accumulation and whole genome sequencing. Our analysis reveals new features of untargeted SOS-mutagenesis, showing how MMR alters its spectrum, sequence specificity, and strand-bias. Our data support a model where the EPPs prefer to act on the lagging strand of the replication fork, producing base pair mismatches that are differentially repaired by MMR depending on the type of mismatch.

"One for All": Functional Transfer of OMV-Mediated Polymyxin B Resistance From Salmonella enterica sv. Typhi ΔtolR and ΔdegS to Susceptible Bacteria.

The appearance of multi-resistant strains has contributed to reintroducing polymyxin as the last-line therapy. Although polymyxin resistance is based on bacterial envelope changes, other resistance mechanisms are being reported. Outer membrane vesicles (OMVs) are nanosized proteoliposomes secreted from the outer membrane of Gram-negative bacteria. In some bacteria, OMVs have shown to provide resistance to diverse antimicrobial agents either by sequestering and/or expelling the harmful agent from the bacterial envelope. Nevertheless, the participation of OMVs in polymyxin resistance has not yet been explored in S. Typhi, and neither OMVs derived from hypervesiculating mutants. In this work, we explored whether OMVs produced by the hypervesiculating strains Salmonella Typhi ΔrfaE (LPS synthesis), ΔtolR (bacterial envelope) and ΔdegS (misfolded proteins and σE activation) exhibit protective properties against polymyxin B. We found that the OMVs extracted from S. Typhi ΔtolR and ΔdegS protect S. Typhi WT from polymyxin B in a concentration-depending manner. By contrast, the protective effect exerted by OMVs from S. Typhi WT and S. Typhi ΔrfaE is much lower. This effect is achieved by the sequestration of polymyxin B, as assessed by the more positive Zeta potential of OMVs with polymyxin B and the diminished antibiotic’s availability when coincubated with OMVs. We also found that S. Typhi ΔtolR exhibited an increased MIC of polymyxin B. Finally, we determined that S. Typhi ΔtolR and S. Typhi ΔdegS, at a lesser level, can functionally and transiently transfer the OMV-mediated polymyxin B resistance to susceptible bacteria in cocultures. This work shows that mutants in genes related to OMVs biogenesis can release vesicles with improved abilities to protect bacteria against membrane-active agents. Since mutations affecting OMV biogenesis can involve the bacterial envelope, mutants with increased resistance to membrane-acting agents that, in turn, produce protective OMVs with a high vesiculation rate (e.g., S. Typhi ΔtolR) can arise. Such mutants can functionally transfer the resistance to surrounding bacteria via OMVs, diminishing the effective concentration of the antimicrobial agent and potentially favoring the selection of spontaneous resistant strains in the environment. This phenomenon might be considered the source for the emergence of polymyxin resistance in an entire bacterial community.

Photochemical-induced phase transitions in photoactive semicrystalline polymers.

The emergent photoactive materials obtained through photochemistry make it possible to directly convert photon energy to mechanical work. There has been much recent work in developing appropriate materials, and a promising system is semicrystalline polymers of the photoactive molecule azobenzene. We develop a phase field model with two order parameters for the crystal-melt transition and the trans-cis photoisomerization to understand such materials, and the model describes the rich phenomenology. We find that the photoreaction rate depends sensitively on temperature: At temperatures below the crystal-melt transition temperature, photoreaction is collective, requires a critical light intensity, and shows an abrupt first-order phase transition manifesting nucleation and growth; at temperatures above the transition temperature, photoreaction is independent and follows first-order kinetics. Further, the phase transition depends significantly on the exact forms of spontaneous strain during the crystal-melt and trans-cis transitions. A nonmonotonic change of photopersistent cis ratio with increasing temperature is observed accompanied by a reentrant crystallization of trans below the melting temperature. A pseudo phase diagram is subsequently presented with varying temperature and light intensity along with the resulting actuation strain. These insights can assist the further development of these materials.

Layer number dependent ferroelasticity in 2D Ruddlesden\u2013Popper organic-inorganic hybrid perovskites

Ferroelasticity represents material domains possessing spontaneous strain that can be switched by external stress. Three-dimensional perovskites like methylammonium lead iodide are determined to be ferroelastic. Layered perovskites have been applied in optoelectronic devices with outstanding performance. However, the understanding of lattice strain and ferroelasticity in layered perovskites is still lacking. Here, using the in-situ observation of switching domains in layered perovskite single crystals under external strain, we discover the evidence of ferroelasticity in layered perovskites with layer number more than one, while the perovskites with single octahedra layer do not show ferroelasticity. Density functional theory calculation shows that ferroelasticity in layered perovskites originates from the distortion of inorganic octahedra resulting from the rotation of aspherical methylammonium cations. The absence of methylammonium cations in single layer perovskite accounts for the lack of ferroelasticity. These ferroelastic domains do not induce non-radiative recombination or reduce the photoluminescence quantum yield.

Influence of Sb2O3 doping on the sintering and polarization characteristics of PbTiO3 ceramic materials

In this paper, the effect of Sb2O3 doping on the sintering and polarization stability of PbTiO3 ceramics was investigated. The Sb2O3-doped PbTiO3 ceramic materials were prepared viaa conventional piezoelectric ceramic processing. The results showed that the as-prepared PbTiO3 ceramics exhibit a good sintering stability without cracking during sintering because of reducing spontaneous strain stemmed from decrease the tetragonal degree of PbTiO3 by Sb2O3 doping. Furthermore, the polarization stability of Sb2O3-doped PbTiO3 ceramics was considerably enhanced by the relaxation of strain and stress concentration during poling stemmed from the formation of good microstructure with fine grain and high density, and by decreasing the loss stemmed from reduction of oxygen vacancy concentration due to the substitution of Sb[Formula: see text] ions for Ti[Formula: see text] ions under a polarization condition with temperature of 130–150[Formula: see text]C and applied electric field of 4.5–5.5 kV/mm, and its yield of polarization is achieved ca. 80%.

Role of correlated disorder on structural stability and functional properties in [formula omitted

In perovskites, correlated disorder arises due to chemical substitution and often stimulates the functional properties of these materials. Powder neutron diffraction measurements have been used in conjunction with electrical measurements to investigate the effect of correlated disorder in (1−x)NaNbO3−(x)BaTiO3 (NNBTx) solid solution by partially substituting the Ba site with Ca. The effect of correlated disorder on competition and cooperation between polar and antiferrodistortive mode has been investigated. Enhanced dielectric constant (by three times) is observed compared to NNBTx. Emergence/vanishing of diffraction peaks along with change in the intensities is observed in powder neutron diffraction data of (1−x)NaNbO3−x(Ba0.7Ca0.3)TiO3 (NNBCTx). Analysis of this data suggests a structural phase transition with composition change (x), while the phase stability of functional ferroelectric phase at room temperature is extended to lower temperatures. It has also been found that there is a gradual weakening of antiferrodistortive mode (R4+) and presence of spontaneous lattice strain with increasing x. The structural parameters of low-temperature orthorhombic phase of NNBCT05 are modeled in the framework of Grüneisen approximation with a Debye model for the internal energy.

A PolyQ Membrane Protein of Vibrio cholerae Acts as the Receptor for Phage Infection.

Bacteriophage VP1 is a typing phage used for the phage subtyping of Vibrio cholerae O1 biotype El Tor, but the molecular mechanisms of its receptor recognition and the resistance of its host to infection are mostly unknown. In this study, we aimed to identify the host receptor and its role in resistance in natural VP1-resistant strains. Generating spontaneous resistance mutations and genome sequencing mutant strains found the polyQ protein VcpQ, which carries 46 glutamine residues in its Q-rich region, to be responsible for infection by VP1. VcpQ is a membrane protein and possibly forms homotrimers. VP1 adsorbed to V. cholerae through VcpQ. Sequence comparisons showed that 72% of natural VP1-resistant strains have fewer glutamines in the VcpQ Q-rich stretch than VP1-sensitive strains. This difference did not affect the membrane location and oligomer of VcpQ but abrogated VP1 adsorption. These mutant VcpQs did not recover VP1 infection sensitivity in a V. cholerae strain with vcpQ deleted. Our study revealed that the polyQ protein VcpQ is responsible for the binding of VP1 during its infection of V. cholerae and that glutamine residue reduction in VcpQ affects VP1 adsorption to likely be the main cause of VP1 resistance in natural resistant strains. The physiological functions of this polyQ protein in bacteria need further clarification; however, mutations in the polyQ stretch may endow V. cholerae with phage resistance and enhance survival against VP1 or related phages.IMPORTANCE Receptor recognition and binding by bacteriophage are the first step for its infection of bacterial cells. In this study, we found the Vibrio cholerae subtyping phage VP1 uses a polyQ protein named VcpQ (V. cholerae polyQ protein) as the receptor for VP1 infection. Our study reveals the receptor's recognition of phage VP1 during its adsorption and the VP1 resistance mechanism of the wild resistant V. cholerae strains bearing the mutagenesis in the receptor VcpQ. These mutations may confer the survival advantage on these resistant strains in the environment containing VP1 or its similar phages.

Efficient IL-2R signaling differentially affects the stability, function, and composition of the regulatory T-cell pool

Signaling via interleukin-2 receptor (IL-2R) is a requisite for regulatory T (Treg) cell identity and function. However, it is not completely understood to what degree IL-2R signaling is required for Treg cell homeostasis, lineage stability and function in both resting and inflammatory conditions. Here, we characterized a spontaneous mutant mouse strain endowed with a hypomorphic Tyr129His variant of CD25, the α-chain of IL-2R, which resulted in diminished receptor expression and reduced IL-2R signaling. Under noninflammatory conditions, Cd25Y129H mice harbored substantially lower numbers of peripheral Treg cells with stable Foxp3 expression that prevented the development of spontaneous autoimmune disease. In contrast, Cd25Y129H Treg cells failed to efficiently induce immune suppression and lost lineage commitment in a T-cell transfer colitis model, indicating that unimpaired IL-2R signaling is critical for Treg cell function in inflammatory environments. Moreover, single-cell RNA sequencing of Treg cells revealed that impaired IL-2R signaling profoundly affected the balance of central and effector Treg cell subsets. Thus, partial loss of IL-2R signaling differentially interferes with the maintenance, heterogeneity, and suppressive function of the Treg cell pool.

Composition, Thermal Expansion and Phase Transitions in Framework Silicates: Revisitation and Review of Natural and Synthetic Analogues of Nepheline-, Feldspar- and Leucite-Mineral Groups

Framework silicates form about 70% of the Earth’s crust, mainly feldspars ~50–60% and quartz ~10–15%. Less-abundant feldspathoids include nepheline-, leucite-, and sodalite-group minerals, rich in structurally challenging properties. This review paper deals with anhydrous feldspar-, nepheline-, and leucite/pollucite groups, emphasising the importance of parallel studies on natural and synthetic samples. Four topics are covered. For decades, petrologists have analysed nephelines and recalculated their compositions as endmember molecules but, by not following rules of stuffed-tridymite crystal chemistry, have not estimated reliably the excess SiO2 present in solid solution. Some materials scientists make similar mistakes, and a new approach is described here. Synthesis studies of analogue feldspars, nephelines, and leucite/pollucites led to collaborative studies, mainly using laboratory and synchrotron X-ray powder diffraction methods at room and elevated temperatures, to study thermal expansion and displacive phase transitions. Such work was recently expanded to address the spontaneous strain relations. Topics covered here include work on nepheline/kalsilite analogues in the system SrAl2O4—BaAl2O4; thermal expansion of (K,Na)Al-, RbAl-, RbGa-, and SrAl-feldspars; and thermal expansion and phase transitions in analogue leucites KGaSi2O6 (tetragonal to cubic) and K2MgSi5O12 (monoclinic to orthorhombic). Results are reviewed in the context of research published in mineralogical and more-widely in physical sciences journals.

Isolation of novel alcohol-tolerant spontaneous mutant strains from sake yeast Kyokai no. 6 and no. 7, and their brewing characteristics

Isolation of novel alcohol-tolerant spontaneous mutant strains from sake yeast Kyokai no. 6 and no. 7, and their brewing characteristics

An unprecedented hexagonal double perovskite organic-inorganic hybrid ferroelastic material: (piperidinium)2[KBiCl6

An unprecedented A2MIMIIIX6-type double perovskite adopting a fully hexagonal BaNiO3-type structure, (piperidinium)2[KBiCl6], undergoes a 2/mF1[combining macron] ferroelastic phase transition at 285 K with a spontaneous strain of 0.0615, arising from the order-disorder transition of organic cations together with the synchronous displacement of inorganic chains.

Order–disorder, ferroelasticity and mobility of domain walls in multiferroic Cu–Cl boracite

Domain walls in Cu–Cl boracite develop as a consequence of an improper ferroelastic, improper ferroelectric transition, and have attracted close interest because some are conductive and all can be mechanically written and repositioned by application of an electric field. The phase transition and its associated dynamical properties have been analysed here from the perspective of strain and elasticity. Determination of spontaneous strains from published lattice parameter data has allowed the equilibrium long-range order parameter for F 3c → Pca21 to be modelled simply as being close to the order–disorder limit. High acoustic loss in the cubic phase, revealed by resonant ultrasound spectroscopy, is consistent with the presence of dynamical microdomains of the orthorhombic structure with relaxation times in the vicinity of ∼10−5–10−6 s. Low acoustic loss in the stability field of the orthorhombic structure signifies, on the other hand, that ferroelastic twin walls which develop as a consequence of the order–disorder process are immobile on this time scale. A Debye loss peak accompanied by ∼1% elastic stiffening at ∼40 K is indicative of some freezing of defects which couple with strain or of some more intrinsic freezing process. The activation energy of ⩾∼0.01–0.02 eV implies a mechanism which could involve strain relaxation clouds around local ferroelectric dipoles or freezing of polarons that determine the conductivity of twin walls.