Life path analysis: scaling indicates priming effects of social and habitat factors on dispersal distances

1. Movements of many animals along a life-path can be separated into repetitive ones within home ranges and transitions between home ranges. We sought relationships of social and environmental factors with initiation and distance of transition movements in 114 buzzards Buteo buteo that were marked as nestlings with long-life radio tags. 2. Ex-natal dispersal movements of 51 buzzards in autumn were longer than for 30 later in their first year and than 35 extra-natal movements between home ranges after leaving nest areas. In the second and third springs, distances moved from winter focal points by birds that paired were the same or less than for unpaired birds. No post-nuptial movement exceeded 2 km. 3. Initiation of early ex-natal dispersal was enhanced by presence of many sibs, but also by lack of worm-rich loam soils. Distances travelled were greatest for birds from small broods and with relatively little short grass-feeding habitat near the nest. Later movements were generally enhanced by the absence of loam soils and short grassland, especially with abundance of other buzzards and probable poor feeding habitats (heathland, long grass). 4. Buzzards tended to persist in their first autumn where arable land was abundant, but subsequently showed a strong tendency to move from this habitat. 5. Factors that acted most strongly in ½-km buffers round nests, or round subsequent focal points, usually promoted movement compared with factors acting at a larger scale. Strong relationships between movement distances and environmental characteristics in ½-km buffers, especially during early ex-natal dispersal, suggested that buzzards became primed by these factors to travel far. 6. Movements were also farthest for buzzards that had already moved far from their natal nests, perhaps reflecting genetic predisposition, long-term priming or poor habitat beyond the study area

Detector Description and Performance for the First Coincidence Observations between LIGO and GEO

For 17 days in August and September 2002, the LIGO and GEO interferometer gravitational wave detectors were operated in coincidence to produce their first data for scientific analysis. Although the detectors were still far from their design sensitivity levels, the data can be used to place better upper limits on the flux of gravitational waves incident on the earth than previous direct measurements. This paper describes the instruments and the data in some detail, as a companion to analysis papers based on the first data.Comment: 41 pages, 9 figures 17 Sept 03: author list amended, minor editorial change

Search for Gravitational Waves from Primordial Black Hole Binary Coalescences in the Galactic Halo

We use data from the second science run of the LIGO gravitational-wave detectors to search for the gravitational waves from primordial black hole (PBH) binary coalescence with component masses in the range 0.2--$1.0 M_\odot$. The analysis requires a signal to be found in the data from both LIGO observatories, according to a set of coincidence criteria. No inspiral signals were found. Assuming a spherical halo with core radius 5 kpc extending to 50 kpc containing non-spinning black holes with masses in the range 0.2--$1.0 M_\odot$, we place an observational upper limit on the rate of PBH coalescence of 63 per year per Milky Way halo (MWH) with 90% confidence.Comment: 7 pages, 4 figures, to be submitted to Phys. Rev.

Newton Algorithms for Analytic Rotation: an Implicit Function Approach

component loss criterion, factor analysis, gradient projection algorithm, oblique rotation, orthogonal rotation, orthogonal matrix, planar algorithm, principal components,

Biases and Standard Errors of Standardized Regression Coefficients

asymptotics, bias, consistency, Monte Carlo,

A simple general procedure for orthogonal rotation

factor analysis, quartimax, varimax, orthomax, simultaneous rotation, simultaneous diagonalization, singular value decomposition, pairwise methods, global convergence,

Core area and centre of activity of maned wolves, Chrysocyon brachyurus (Illiger) (Mammalia, Canidae), submitted to supplemental feeding

Based on the finding of remains (tracks, scats, and hairs), an analysis was made of the core area and centre of activity of maned wolves, Chrysocyon brachyurus (Illiger, 1815), living in a private natural reserve in which ecotourism activities are developed and these animals are daily fed bovine meat. A total of 465 samples of remains were recorded. Using the fixed kernel method, the area encompassing all samples recorded was estimated at 25.7 km², yet 50% of all samples were found in an area of only 1.5 km², representing 5.8% of the total area covered. For estimating the core area of the animals, the frequency of occurrence of the samples was determined by superimposing a 50 x 50 m cell grid over a map of the area encompassing all recorded occurrences. Based on the cells containing more than six occurrences, the animals' core area was 0.99 km², which included the place where the animals are fed. The centre of activity was located only 0.50 km from this place. The high negative correlation (r = -0.93, p < 0.05) between the densities of the recorded occurrences and the distances from these to the sanctuary indicates that the core area and centre of activity are conditioned by artificial feeding.<br>A área central e o centro de atividade de lobos-guará, Chrysocyon brachyurus (Illiger, 1815), foram determinados através de seus vestígios (fezes, pegadas e pêlos) em uma reserva natural particular, onde esses animais estão sujeitos à alimentação artificial e sofrem influência de atividades turísticas. No total, foram registrados 465 vestígios, sendo que 65,8% corresponderam à estação seca. Através do método Kernel fixo, a área compreendida por todos os vestígios foi de 25,7 km², sendo que 50% encontravam-se em uma área de apenas 1,5 km², o que representou 5,8% do total da área amostrada. A área central de atividade dos animais foi obtida pelo cálculo da freqüência dos registros dos vestígios através da sobreposição de uma quadrícula subdividida em células de 50 x 50 m sobre a área que abrangia todos os registros. Considerando as células com mais de seis registros a área central de atividade atribuída aos animais foi de 0,99 km², o que abrangeu a sede da reserva onde os animais são alimentados. O centro de atividade localizou-se somente a 0,50 km da sede. A alta correlação negativa (r = -0,93, p < 0,05) obtida entre as densidades dos registros e suas distâncias até a sede da reserva indicaram que o centro de atividade e o tamanho da área de maior intensidade de uso são condicionados pela alimentação artificial