| 1. |
- Amundin, Mats, et al.
(författare)
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Estimating the abundance of the critically endangered Baltic Proper harbour porpoise (Phocoena phocoena) population using passive acoustic monitoring
- 2022
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Ingår i: Ecology and Evolution. - : Wiley. - 2045-7758. ; 12:2
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Tidskriftsartikel (refereegranskat)abstract
- Knowing the abundance of a population is a crucial component to assess its conservationstatus and develop effective conservation plans. For most cetaceans, abundanceestimation is difficult given their cryptic and mobile nature, especially when thepopulation is small and has a transnational distribution. In the Baltic Sea, the numberof harbour porpoises (Phocoena phocoena) has collapsed since the mid-20thcenturyand the Baltic Proper harbour porpoise is listed as Critically Endangered by the IUCNand HELCOM; however, its abundance remains unknown. Here, one of the largestever passive acoustic monitoring studies was carried out by eight Baltic Sea nationsto estimate the abundance of the Baltic Proper harbour porpoise for the first time. Bylogging porpoise echolocation signals at 298 stations during May 2011–April2013,calibrating the loggers’ spatial detection performance at sea, and measuring the clickrate of tagged individuals, we estimated an abundance of 71–1105individuals (95% CI,point estimate 491) during May–Octoberwithin the population's proposed managementborder. The small abundance estimate strongly supports that the Baltic Properharbour porpoise is facing an extremely high risk of extinction, and highlights theneed for immediate and efficient conservation actions through international cooperation.It also provides a starting point in monitoring the trend of the populationabundance to evaluate the effectiveness of management measures and determine itsinteractions with the larger neighboring Belt Sea population. Further, we offer evidencethat design-basedpassive acoustic monitoring can generate reliable estimatesof the abundance of rare and cryptic animal populations across large spatial scales.
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| 2. |
- Andersson, C. David, 1978-, et al.
(författare)
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Influence of Enantiomeric Inhibitors on the Dynamics of Acetylcholinesterase Measured by Elastic Incoherent Neutron Scattering
- 2018
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 122:36, s. 8516-8525
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Tidskriftsartikel (refereegranskat)abstract
- The enzyme acetylcholinesterase (AChE) is essential in humans and animals because it catalyzes the breakdown of the nerve-signaling substance acetylcholine. Small molecules that inhibit the function of AChE are important for their use as drugs in the, for example, symptomatic treatment of Alzheimer's disease. New and improved inhibitors are warranted, mainly because of severe side effects of current drugs. In the present study, we have investigated if and how two enantiomeric inhibitors of AChE influence the overall dynamics of noncovalent complexes, using elastic incoherent neutron scattering. A fruitful combination of univariate models, including a newly developed non-Gaussian model for atomic fluctuations, and multivariate methods (principal component analysis and discriminant analysis) was crucial to analyze the fine details of the data. The study revealed a small but clear increase in the dynamics of the inhibited enzyme compared to that of the noninhibited enzyme and contributed to the fundamental knowledge of the mechanisms of AChE-inhibitor binding valuable for the future development of inhibitors.
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| 3. |
- Karlsson, Maths, et al.
(författare)
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Quasielastic neutron scattering of hydrated BaZr(0.90)A(0.10)O(2.95) (A = Y and Sc)
- 2009
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Ingår i: Solid State Ionics. - : Elsevier BV. - 0167-2738. ; 180:1, s. 22-28
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Tidskriftsartikel (refereegranskat)abstract
- Proton motions in hydrated proton conducting perovskites BaZr(0.90)A(0.10)O(2.95) (A = Y and Sc) have been investigated using quasielastic neutron scattering. The results reveal a localized motion on the ps time scale and with an activation energy of similar to 10-30 meV, in both materials. The temperature dependence of the total mean square displacement of the protons shows an onset of this motion at a temperature of about 300 K. The low activation energy, much lower than the activation energy for the macroscopic proton conductivity, suggests that this motion is not the rate-limiting process for the long-range proton diffusion, i.e. it is not linked to the two materials significantly different proton conductivities. In fact, a comparison of the QENS results with density functional theory calculations indicates that for both materials the observed motion may be ascribed to intra-octahedral proton transfers occurring close to a dopant atom. (C) 2008 Elsevier B.V. All rights reserved.
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| 4. |
- Perrichon, Adrien, 1988, et al.
(författare)
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Proton Diffusion Mechanism in Hydrated Barium Indate Oxides
- 2023
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Ingår i: Chemistry of Materials. - 1520-5002 .- 0897-4756. ; 35:17, s. 6713-6725
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Tidskriftsartikel (refereegranskat)abstract
- We report on quasielastic neutron scattering (QENS) andab initiomolecular dynamics (AIMD) simulations of the mechanism of proton diffusionin the partially and fully hydrated barium indate oxide proton conductorsBa(2)In(2)O(5)(H2O)( x ) (x = 0.30 and 0.92). Structurally,these materials are featured by an intergrowth of cubic and "pseudo-cubic"layers of InO6 octahedra, wherein two distinct proton sites,H(1) and H(2), are present. We show that the main localized dynamicsof these protons can be described as rotational diffusion of O-H(1)species and H(2) proton transfers between neighboring oxygen atoms.The mean residence times of both processes are in the order of picosecondsin the two studied materials. For the fully hydrated material, Ba2In2O5(H2O)(0.92), we also reveal the presence of a third proton site, H(3), whichbecomes occupied upon increasing the temperature and serves as a saddlestate for the interexchange between H(1) and H(2) protons. Crucially,the occupation of the H(3) site enables long-range diffusion of protons,which is highly anisotropic in nature and occurs through a two-dimensionalpathway. For the partially hydrated material, Ba2In2O5(H2O)(0.30), the occupationof the H(3) site and subsequent long-range diffusion are not observed,which is rationalized by hindered dynamics of H(2) protons in thevicinity of oxygen vacancies. A comparison to state-of-the-art proton-conductingoxides, such as barium zirconate-based materials, suggests that thegenerally lower proton conductivity in Ba2In2O5(H2O)( x ) is dueto a large occupation of the H(1) and H(2) sites, which, in turn,means that there are few sites available for proton diffusion. Thisinsight suggests that the chemical substitution of indium by cationswith higher oxidation states offers a novel route toward higher protonconductivity because it reduces the proton site occupancy while preservingan oxygen-vacancy-free structure.
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| 5. |
- Tsapatsaris, Nikolaos, et al.
(författare)
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Polymorphic drugs examined with neutron spectroscopy: Is making more stable forms really that simple?
- 2013
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Ingår i: Chemical Physics. - : Elsevier BV. - 0301-0104. ; 427, s. 124-128
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Tidskriftsartikel (refereegranskat)abstract
- Understanding polymorphism in pharmaceutical ingredients is a long-standing challenge in formulation science. A well-known example is paracetamol, C8H9NO2. The marketed stable form I crystallizes with corrugated molecular layers. In contrast, form II, which is thermodynamically favorable at high pressures, has relatively planar layers that can slip over each other without difficulty, but is metastable at ambient conditions. By means of inelastic neutron scattering we demonstrated that the lattice modes of form II exhibit a sudden 1 meV energy shift at 300 K under a pressure of ca 0.4 GPa. Moreover, evidence of an increase of the vibrational energy in both polymorphs was found, which was accompanied, in form I, by an unexpectedly weak increase of the tunnel splitting. These results indicate an anisotropy of the potential surface probed by the methyl rotor, and are discussed in relation to the differences of the strength of the hydrogen bond environment for each polymorph. (C) 2013 Elsevier B. V. All rights reserved.
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