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Population-based incremental learning with associative memory for dynamic environments
Copyright © 2007 IEEE. Reprinted from IEEE Transactions on Evolutionary Computation.
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By choosing to view this document, you agree to all provisions of the copyright laws protecting it.In recent years there has been a growing interest in studying evolutionary algorithms (EAs) for dynamic optimization problems (DOPs) due to its importance in real world applications. Several approaches, such as the memory and multiple population schemes, have been developed for EAs to address dynamic problems. This paper investigates the application of the memory scheme for population-based incremental learning (PBIL) algorithms, a class of EAs, for DOPss. A PBIL-specific associative memory scheme, which stores best solutions as well as corresponding environmental information in the memory, is investigated to improve its adaptability in dynamic environments. In this paper, the interactions between the memory scheme and random immigrants, multi-population, and restart schemes for PBILs in dynamic environments are investigated. In order to better test the performance of memory schemes for PBILs and other EAs in dynamic environments, this paper also proposes a dynamic environment generator that can systematically generate dynamic environments of different difficulty with respect to memory schemes. Using this generator a series of dynamic environments are generated and experiments are carried out to compare the performance of investigated algorithms. The experimental results show that the proposed memory scheme is efficient for PBILs in dynamic environments and also indicate that different interactions exist between the memory scheme and random immigrants, multi-population schemes for PBILs in different dynamic environments
Experimental study on population-based incremental learning algorithms for dynamic optimization problems
Copyright @ Springer-Verlag 2005.Evolutionary algorithms have been widely used for stationary optimization problems. However, the environments of real world problems are often dynamic. This seriously challenges traditional evolutionary algorithms. In this paper, the application of population-based incremental learning (PBIL) algorithms, a class of evolutionary algorithms, for dynamic problems is investigated. Inspired by the complementarity mechanism in nature a Dual PBIL is proposed, which operates on two probability vectors that are dual to each other with respect to the central point in the genotype space. A diversity maintaining technique of combining the central probability vector into PBIL is also proposed to improve PBILs adaptability in dynamic environments. In this paper, a new dynamic problem generator that can create required dynamics from any binary-encoded stationary problem is also formalized. Using this generator, a series of dynamic problems were systematically constructed from several benchmark stationary problems and an experimental study was carried out to compare the performance of several PBIL algorithms and two variants of standard genetic algorithm. Based on the experimental results, we carried out algorithm performance analysis regarding the weakness and strength of studied PBIL algorithms and identified several potential improvements to PBIL for dynamic optimization problems.This work was was supported by
UK EPSRC under Grant GR/S79718/01
Dual population-based incremental learning for problem optimization in dynamic environments
Copyright @ 2003 Asia Pacific Symposium on Intelligent and Evolutionary SystemsIn recent years there is a growing interest in the research of evolutionary algorithms for dynamic optimization problems since real world problems are usually dynamic, which presents serious challenges to traditional evolutionary algorithms. In this paper, we investigate the application of Population-Based Incremental Learning (PBIL) algorithms, a class of evolutionary algorithms, for problem optimization under dynamic environments. Inspired by the complementarity mechanism in nature, we propose a Dual PBIL that operates on two probability vectors that are dual to each other with respect to the central point in the search space. Using a dynamic problem generating technique we generate a series of dynamic knapsack problems from a randomly generated stationary knapsack problem and carry out experimental study comparing the performance of investigated PBILs and one traditional genetic algorithm. Experimental results show that the introduction of dualism into PBIL improves its adaptability under dynamic environments, especially when the environment is subject to significant changes in the sense of genotype space
Anthropometry and physical characteristics in English premiership women’s rugby
Rugby union is a field-based team sport characterized by repeated high-intensity activities (sprinting, agility and collisions) combined with periods of lower intensity activities (walking and jogging). Based on positional differences and match demands, athletes are generally grouped as forwards (front row, second row and back row) and backs (scrum half, inside backs and outside backs). English premiership women’s rugby union has been continually growing in popularity and gaining participants every year. Besides increases in participation, the standard of women’s rugby union has improved due to increased investment, which enabled international women rugby players to become semi or fully professional. The growth of women’s rugby union has naturally led to an increase in scientific interest and research. Research into women’s rugby union has focused on match demands, anthropometry, and physical characteristics.
In study 1, a systematic search of literature was undertaken to review existing research regarding identifying the characteristics to become a competitive women’s rugby union player. The result revealed that a total of 25 studies focused on identifying and discussing match demands, anthropometry, and physical characteristics. Forwards were found to have participated in more collisions, were heavier, and demonstrated greater absolute strength. Backs engaged in more high-speed running, were leaner, aerobically fitter, and relatively stronger.
In study 2, anthropometry using dual-X-ray absorptiometry and physical characteristics made up of strength and power tests (countermovement jump, drop jump, and isometric mid-thigh pull) were investigated and grouped by position. Overall, forwards had significantly (p 0.5) jump height, reactive strength index modified, and shorter drop jump contact time.
In study 3, Seasonal changes of anthropometry and physical characteristics were observed throughout pre-, mid- and post-season. Based on the tests used in study 1, statistically significant differences (p 0.5) in lean mass (mid- > pre-season), reactive strength index modified (post- > mid-season), time to take-off (post- 0.5) in lean mass (post- > pre-season) and drop jump flight time (pre- < mid- and post-season) throughout the season.
In study 4, sprint performance and kinematics were discussed between positions and fast, moderate, and slow groups based on the split times of acceleration and top speed were formed. Findings demonstrate that during acceleration backs performed statistically significantly higher velocity, step rate, step velocity, and shorter contact time (p 0.80). Forwards, despite being slower, still produced moderately higher to statistically significantly higher initial and top speed momentum (p 0.7) due to higher body mass. When comparing different speed groups, faster athletes used a shorter contact time (g = 1.58 to 1.64) to generate a moderate to larger toe-off thigh angle (g =0.57 to 1.00), and a longer flight length (g =1.21 to 1.34) to create a longer step length (g = 1.12 to 1.19) in both acceleration and top speed.
In study 5, seasonal changes of sprint performance and kinematics were observed throughout pre-, mid- and post-season. Velocity, initial momentum, flight time, toe off distance, and flight length statistically significantly decreased (p 1.33) in acceleration from pre- to mid-season. A similar trend was found in top speed, and step length, step velocity, foot strike distance, toe-off distance, and contact length all statistically significantly decreased (p 1.87) from pre-to mid-season. From mid- to post-season, trivial practical differences were found in acceleration velocity but large practical differences were observed in contact time, flight time, toe-off distance, and flight length (g > 0.90). Top speed had a moderate increase (g = 0.68) from mid- to post-season, and step velocity, foot strike distance, toe-off distance, contact and flight length all statistically significantly increased (p 1.38).
In study 6, change of direction ability and relationship was determined between positions. Further investigation using different speed groups was again undertaken and were based on the time of the 505 test, again split into thirds. Dominant side of the 505 test was based on the faster time compared between both left and right turn recorded during the test. Backs demonstrated statistically significantly faster 505 times in both the dominate and non-dominate side compared to forwards (p < 0.05, g = 0.93 and 1.06). However, no statistically significant differences were found in change of direction deficit between positions. Forwards’ dominant side 505 time demonstrated a significant positive relationship (r = 0.67) with body mass. Furthermore, forwards’ linear velocity had significant negative relationship (r = -0.70) with dominate side 505 time, but a positive relationship with dominate side change of direction deficit (r = 0.60). In contrast, no significant relationship in backs was found between linear velocity and dominate side 505 for backs. Backs linear sprint velocity was shown to have a significant positive relationship with both dominate (r = 0.60) and non-dominate side (r = 0.71) change of direction deficit. When observing speed group differences, faster athletes had statistically significantly lighter body mass, faster linear sprint, and non-dominate side 505 time (p < 0.05, g = 1.35 to 2.15).
In study 7, seasonal changes of change of direction ability were observed between mid- and post-season. No pre-season data was collected due to the impact the COVID 19 pandemic had to professional sport. Besides large practical increase in body mass and initial momentum, only small practical increases was found in 505 time on both the dominate and non-dominate side (g = 0.37 and 0.41).
In conclusion, the findings of this thesis determined the match demands that women rugby players face in different position. The results demonstrated that forwards, although slower than backs, have higher lean mass and fat mass, generated higher momentum and absolute peak force, which support positional match demands for forwards to face more frequent collisions. Backs were found to be leaner, faster in both linear and change of direction sprints, and were able to produce relative peak force similar to forwards. In addition, the results supported match demand studies identifying backs have more opportunity to reach high speed but also need the strength to face higher collision forces. The longitudinal studies determined that anthropometry characteristics are maintained throughout the season with only a small practical increase in lean mass from pre- to mid-season. However, in physical characteristics, both power tests and sprint performance results showed a decrease from pre- to mid-season and an increase from mid- to post-season. Lastly, as both sprinting and change of direction are motor skills rather than proxy measures of force and power output, understanding the kinematics in sprinting and change of direction can be used to identify common characteristics in fast athletes from which training can be devised and monitored. Overall, these finding represent novel contributions to women’s rugby union literature as well as providing insights and baseline data for future research and practitioners to make informed recruitment and training decisions
Influence of low-level Pr substitution on the superconducting properties of YBa2Cu3O7-delta single crystals
We report on measurements on Y1-xPrxBa2Cu3O7-delta single crystals, with x
varying from 0 to 2.4%. The upper and the lower critical fields, Hc2 and Hc1,
the Ginzburg-Landau parameter and the critical current density, Jc(B), were
determined from magnetization measurements and the effective media approach
scaling method. We present the influence of Pr substitution on the pinning
force density as well as on the trapped field profiles analyzed by Hall probe
scanning.Comment: 4 pages, 5 figures, accepted for publication in J. Phys. Conf. Se
In-plane thermal conductivity of large single crystals of Sm-substituted (YSm)BaCuO
We have investigated the in-plane thermal conductivity of
large single crystals of optimally oxygen-doped
(Y,Sm)BaCuO (=0, 0.1, 0.2 and 1.0)
and YBa(CuZn)O(=0.0071) as functions
of temperature and magnetic field (along the c axis). For comparison, the
temperature dependence of for as-grown crystals with the
corresponding compositions are presented.
The nonlinear field dependence of for all crystals was observed
at relatively low fields near a half of . We make fits of the
data to an electron contribution model, providing both the mean
free path of quasiparticles and the electronic thermal conductivity
, in the absence of field. The local lattice distortion due to the
Sm substitution for Y suppresses both the phonon and electron contributions. On
the other hand, the light Zn doping into the CuO planes affects solely
the electron component below , resulting in a substantial decrease in
.Comment: 7 pages,4 figures,1 tabl
Universal Scaling of the Neel Temperature of Near-Quantum-Critical Quasi-Two-Dimensional Heisenberg Antiferromagnets
We use a quantum Monte Carlo method to calculate the Neel temperature T_N of
weakly coupled S=1/2 Heisenberg antiferromagnetic layers consisting of coupled
ladders. This system can be tuned to different two-dimensional scaling regimes
for T > T_N. In a single-layer mean-field theory,
\chi_s^{2D}(T_N)=(z_2J')^{-1}, where \chi_s^{2D} is the exact staggered
susceptibility of an isolated layer, J' the inter-layer coupling, and z_2=2 the
layer coordination number. With a renormalized z_2, we find that this
relationship applies not only in the renormalized-classical regime, as shown
previously, but also in the quantum-critical regime and part of the
quantum-disordered regime. The renormalization is nearly constant; k_2 ~
0.65-0.70. We also study other universal scaling functions.Comment: 4 pages, 4 figure
Magnetic Excitations of Stripes and Checkerboards in the Cuprates
We discuss the magnetic excitations of well-ordered stripe and checkerboard
phases, including the high energy magnetic excitations of recent interest and
possible connections to the "resonance peak" in cuprate superconductors. Using
a suitably parametrized Heisenberg model and spin wave theory, we study a
variety of magnetically ordered configurations, including vertical and diagonal
site- and bond-centered stripes and simple checkerboards. We calculate the
expected neutron scattering intensities as a function of energy and momentum.
At zero frequency, the satellite peaks of even square-wave stripes are
suppressed by as much as a factor of 34 below the intensity of the main
incommensurate peaks. We further find that at low energy, spin wave cones may
not always be resolvable experimentally. Rather, the intensity as a function of
position around the cone depends strongly on the coupling across the stripe
domain walls. At intermediate energy, we find a saddlepoint at for
a range of couplings, and discuss its possible connection to the "resonance
peak" observed in neutron scattering experiments on cuprate superconductors. At
high energy, various structures are possible as a function of coupling strength
and configuration, including a high energy square-shaped continuum originally
attributed to the quantum excitations of spin ladders. On the other hand, we
find that simple checkerboard patterns are inconsistent with experimental
results from neutron scattering.Comment: 11 pages, 13 figures, for high-res figs, see
http://physics.bu.edu/~yaodx/spinwave2/spinw2.htm
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