Measurement of the distribution of site enhancements in surface-enhanced Raman scattering

On nanotextured noble-metal surfaces, surface-enhanced Raman scattering (SERS) is observed, where Raman scattering is enhanced by a factor, G, that is frequently about one million, but underlying the factor G is a broad distribution of local enhancement factors, eta. We have measured this distribution for benzenethiolate molecules on a 330-nanometer silver-coated nanosphere lattice using incident light of wavelength 532 nanometers. A series of laser pulses with increasing electric fields burned away molecules at sites with progressively decreasing electromagnetic enhancement factors. The enhancement distribution P(eta)deta was found to be a power law proportional to (eta)(-1.75), with minimum and maximum values of 2.8 x 10(4) and 4.1 x 10(10), respectively. The hottest sites (eta >10(9)) account for just 63 in 1,000,000 of the total but contribute 24% to the overall SERS intensity.     

Heritability of inflorescence and floret traits in gerbera

Summary Heritability, repeatability, and components of variance were estimated for 68 morphological characters describing the inflorescence, scape, and florets of Gerbera hybrida. The heritability estimates were generally moderate to high for simple dimension characters and characters which were the mean of several measurements, low to moderate for ratio and composite characters, and low for enumeration characters and characters describing the intraplant variation of traits. The repeatability estimates were generally low for intraplant variation characters, moderate for simple ratio characters, and largest for composite and mean characters. For most of the characters, the variance among inflorescences from the same plant was the largest portion of the total phenotypic variance.     

Production and storage of sperm from the black sea bass Centropristis striata L

Black sea bass Centropristis striata L. are protogynous hermaphrodites that develop and spawn as females before changing sex to male. Since all fish eventually become males, determining the relationship between sperm production, sperm quality and seasonal changes in plasma levels of testosterone (T) and 11‐ketotestosterone (11‐KT) could be useful for identifying appropriate males to maintain as broodstock. Milt and blood samples were collected three times during an 8‐week spawning season. Milt volume (3.5±0.76 mL kg^?1), sperm density (3.2 × 10⁸± 0.31 cells mL^?1), sperm production [11 × 10⁸±3.4 cells kg^?1 body weight (BW)] and sperm motility (80±0.6%) were at their highest during the first sampling interval and coincided with the highest 11‐KT levels (1.0± 0.11 ng mL^?1). All of the sperm indices decreased to their lowest levels during the final 3 weeks of the study. Sperm viability was highly correlated (adjusted R²=0.84) with sperm motility. Sperm cryopreserved in modified Mounib's extender (MME) had the highest post‐thaw motility compared with two other extenders. Post‐thaw motility of sperm cryopreserved in MME was not different from fresh after 90 days of storage. There was no difference in fertilization rates between fresh (69±2.4%) and post‐thaw (67±4.1%) sperm samples taken from the same male or among males. These results demonstrate that the quality of black sea bass spermatozoa is higher earlier in the spawning season and that acceptable post‐thaw fertilization rates can be obtained from cryopreserved sperm.     

Diversity of microsporidia (Fungi: Microsporidia) among captive great apes in European zoos and African sanctuaries: evidence for zoonotic transmission?

Abstract: Two hundred and seventeen captive great apes (150 chimpanzees, Pan troglodytes; 14 bonobos, Pan paniscus; 53 western gorillas, Gorilla gorilla) and 20 personnel from thirteen European zoos and two African sanctuaries were sampled and examined in order to determine the occurrence ofEnterocytozoon bieneusi and species of Encephalitozoon in faecal specimens and to compare the epidemiological situation between zoos and sanctuaries. Microsporidia were detected at all sampling sites. Sequence analyses of ITS amplicons generated by using microsporidia-specific primers determined the presence ofmicrosporidia in 87 samples including 13 humans; since two cases of simultaneous occurrence of Encephalitozoon cuniculi and Enterocytozoon bieneusi were identified, 89 full-length ITS sequences were obtained, namely 78 Encephalitozoon cuniculi genotype I, five E. cuniculi genotype II, two E. hellem 1A and four Enterocytozoon bieneusi. No Encephalitozoon intestinalis-positive samples were identified. This is the first report of Encephalitozoon species and Enterocytozoon bieneusi genotypes in captive great apes kept under various conditions and the first record of natural infection with E. hellem in great apes. A comparison of zoos and sanctuaries showed a significantly higher prevalence of microsporidia in sanctuaries (P<0.001), raising a question about the factors affecting the occurrence of microsporidia in epidemiologically and sanitarily comparable types of facilities.     

A Bayesian multinomial model for analyzing categorical habitat selection data

Modeling the number of uses of discrete habitat types by animals with a multinomial distribution, we illustrate the use of Bayesian methods to estimate selection. An advantage of this approach in assessing selection is the construction of credibility intervals that do not rely on large sample normal theory. In addition, credibility intervals for ranked selection of habitats are easily obtained. Bayes factors and Bayesian p values (posterior predictive values) are used to test the hypothesis of selection for each animal, test selection across all animals and for multiple comparisons among habitats. We compare our method to alternative methods for a real dataset. Freely available WinBUGS software is used to fit the model and test hypotheses.     

Components of genetic variation for cut-flower yield in the Davis Population of Gerbera

Summary Genetic variances for cut-flower yield in Gerbera hybrida were partitioned into additive and dominance components. Mean additive variance was 37.3 with a standard error of 12.9. Mean dominance variance was 12.7 with a standard error of 32.6. The dominance ratio was 0.34. Narrow sense heritability, estimated from these components of variance, averaged 0.42 with a standard error of 0.13. Heritabilities estimated from parent-offspring regression averaged 0.25. Gain from selection was less then expected; realized heritabilities were approximately 0.20.