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Different Pairs (different + pair)
Selected AbstractsFISH mapping and sequence analysis of 87 porcine BAC clonesANIMAL GENETICS, Issue 1 2004R. Anistoroaei Summary Ninety-one bacterial artificial chromosomes (BAC) clones, selected effectively at random from our library, were used as probes for fluorescence in situ hybridization. Of these, 87 clones gave a specific signal in one, two or three different pair(s) of swine metaphase chromosomes. The ends of 35 BAC clones were sequenced in order to obtain information for comparative mapping. Fifteen of them gave useful comparative mapping information. [source] Response Surface Designs for Experiments in BioprocessingBIOMETRICS, Issue 2 2006Steven G. Gilmour Summary Many processes in the biological industries are studied using response surface methodology. The use of biological materials, however, means that run-to-run variation is typically much greater than that in many experiments in mechanical or chemical engineering and so the designs used require greater replication. The data analysis which is performed may involve some variable selection, as well as fitting polynomial response surface models. This implies that designs should allow the parameters of the model to be estimated nearly orthogonally. A class of three-level response surface designs is introduced which allows all except the quadratic parameters to be estimated orthogonally, as well as having a number of other useful properties. These subset designs are obtained by using two-level factorial designs in subsets of the factors, with the other factors being held at their middle level. This allows their properties to be easily explored. Replacing some of the two-level designs with fractional replicates broadens the class of useful designs, especially with five or more factors, and sometimes incomplete subsets can be used. It is very simple to include a few two- and four-level factors in these designs by excluding subsets with these factors at the middle level. Subset designs can be easily modified to include factors with five or more levels by allowing a different pair of levels to be used in different subsets. [source] Individuation of pairs of objects in infancyDEVELOPMENTAL SCIENCE, Issue 4 2007Alan M. Leslie Looking-time studies examined whether 11-month-old infants can individuate two pairs of objects using only shape information. In order to test individuation, the object pairs were presented sequentially. Infants were familiarized either with the sequential pairs, disk-triangle/disk-triangle (XY/XY), whose shapes differed within but not across pairs, or with the sequential pairs, disk-disk/triangle-triangle (XX/YY), whose shapes differed across but not within pairs. The XY/XY presentation looked to adults like a single pair of objects presented repeatedly, whereas the XX/YY presentation looked like different pairs of objects. Following familiarization to these displays, infants were given a series of test trials in which the screen was removed, revealing two pairs of objects in one of two outcomes, XYXY or XXYY. On the first test trial, infants familiarized with the identical pairs (XY/XY) apparently expected a single pair to be revealed because they looked longer than infants familiarized with the distinct pairs (XX/YY). Infants who had seen the distinct pairs apparently expected a double pair outcome. A second experiment showed outcomes of a single XY pair. This outcome is unexpected for XX/YY-familiarized infants but expected for XY/XY-familiarized infants, the reverse of Experiment 1. This time looking times were longer for XX/YY infants. Eleven-month-olds appear to be able to represent not just individual objects but also pairs of objects. These results suggest that if they can group the objects into sets, infants may be able to track more objects than their numerosity limit or available working memory slots would normally allow. We suggest possible small exact numerosity representations that would allow tracking of such sets. [source] Use of terrain variables for mapping gully erosion susceptibility in LebanonEARTH SURFACE PROCESSES AND LANDFORMS, Issue 12 2007Rania Bou Kheir Abstract This paper predicts the geographic distribution and size of gullies across central Lebanon using a geographic information system (GIS) and terrain analysis. Eleven primary (elevation; upslope contributing area; aspect; slope; plan, profile and tangential curvature; flow direction; flow width; flow path length; rate of change of specific catchment area along the direction of flow) and three secondary (steady-state; quasi-dynamic topographic wetness; sediment transport capacity) topographic variables were generated and used along with digital data collected from other sources (soil, geology) to statistically explain gully erosion field measurements. Three tree-based regression models were developed using (1) all variables, (2) primary topographic variables only and (3) different pairs of variables. The best regression tree model combined the steady-state topographic wetness and sediment transport capacity indices and explained 80% of the variability in field gully measurements. This model proved to be simple, quick, realistic and practical, and it can be applied to other areas of the Mediterranean region with similar environmental conditions, thereby providing a tool to help with the implementation of plans for soil conservation and sustainable management. Copyright © 2007 John Wiley & Sons, Ltd. [source] Post-fledging behaviour in Golden Eagles Aquila chrysaetos: onset of juvenile dispersal and progressive distancing from the nestIBIS, Issue 2 2006ALVARO SOUTULLO Thirteen juvenile Golden Eagles Aquila chrysaetos were tracked during their first year of life using satellite telemetry. Distances to the nest attained during that period and the age at the onset of juvenile dispersal were explored. The performance of nine different criteria to determine that age was analysed. In general, after a brief period of restricted movements around the nest, the average distance to the nest increased with time. Maximum distances to the nest ranged between 57.7 and 184.3 km, and were considerably greater in females (mean ± sd, 138.5 ± 44.5 km) than in males (70.5 ± 14.0 km). No sex difference was observed in the age at which that distance was attained (males: 329 ± 32 days, females: 312 ± 20 days). The onset of juvenile dispersal took place around the fifth month of life (September in Spain). Eight of the nine criteria provided similar results, suggesting that in Spain dispersal starts when birds are between 140 and 180 days old, and that the post-nestling period lasts between 60 and 120 days. For future studies, to determine the age at which the onset of juvenile dispersal occurs, we recommend the use of either the first day on which individuals were located beyond the mean distance between nests of different pairs (10 km in our study area), or the date of the record midway between the first and the last location recorded during the month in which the maximum variability in the distance to the nest was observed. [source] Isolation and characterization of polymorphic microsatellites in olive (Olea europaea L.) and their transferability to other genera in the OleaceaeMOLECULAR ECOLOGY RESOURCES, Issue 3 2002R. De La Rosa Abstract Seven polymorphic microsatellites were developed in olive. Six of them came from a genomic library enriched for GA and CA repeat sequences. They showed single locus polymorphism in a set of 23 olive cultivars (from six to nine alleles per locus). Three different pairs of loci were sufficient to discriminate all cultivars. The other polymorphic primer pair was designed from a published sequence for olive lupeol sgutase and revealed just two alleles. The seven primer pairs were tested on two accessions of five other species of the Oleaceae and three, EMO2, EMO13 and EMO90, revealed polymorphism in two, four and three species, respectively. [source] Distinguishing characteristics and vegetative compatibility of Colletotrichum kahawe in comparison with other related species from coffeePLANT PATHOLOGY, Issue 2 2002V. M. P. Varzea On the basis of pathogenicity tests on green berries or hypocotyls of coffee and by morphological and biochemical characteristics in culture, 31 isolates of Colletotrichum were classified into C. kahawe (24 isolates), C. gloeosporioides (six isolates) or C. acutatum (one isolate). Within these groups of isolates, vegetative compatibility groups (VCGs) were determined by complementation tests with mutants in the nitrate assimilation pathway. There were distinct incompatibility barriers between the three species. Among the C. gloeosporioides group, the three isolates tested were self-compatible but incompatible with each other. Within C. kahawe, 18 isolates were self-compatible and only one main VCG was detected. However, partial compatibility in C. kahawe was also indicated by variation in the intensity of heterokaryon formation between different pairs of isolates and between different types of mutant. The existence of only one VCG in C. kahawe is consistent with the low level of variation found in previous work on DNA polymorphism. [source] Six-Month-Old Infants' Categorization of Containment Spatial RelationsCHILD DEVELOPMENT, Issue 3 2003Marianella Casasola Six-month-old infants' ability to form an abstract category of containment was examined using a standard infant categorization task. Infants were habituated to 4 pairs of objects in a containment relation. Following habituation, infants were tested with a novel example of the familiar containment relation and an example of an unfamiliar relation. Results indicate that infants look reliably longer at the unfamiliar versus familiar relation, indicating that they can form a categorical representation of containment. A second experiment demonstrated that infants do not rely on object occlusion to discriminate containment from a support or a behind spatial relation. Together, the results indicate that by 6 months, infants can recognize a containment relation from different angles and across different pairs of objects. [source] | |||||||||||||